Butterflies of Sulawesi

ZV-343 003-268 | vane-wright 04-01-2007 15:47 Page 3
The butterflies of Sulawesi: annotated checklist for

a critical island fauna1
R.I. Vane-Wright & R. de Jong
With contributions from P.R. Ackery, A.C. Cassidy, J.N. Eliot, J.H. Goode, D. Peggie,
R.L. Smiles, C.R. Smith and O. Yata.
Vane-Wright, R.I. & R. de Jong. The butterflies of Sulawesi: annotated checklist for a critical island fauna.
Zool. Verh. Leiden 343, 11.vii.2003: 3-267, figs 1-14, pls 1-16.— ISSN 0024-1652/ISBN 90-73239-87-7.
R.I. Vane-Wright, Department of Entomology, The Natural History Museum, Cromwell Road, London
SW7 5BD, UK;
R. de Jong, Department of Entomology, National Museum of Natural History, PO Box 9517, 2300 RA
Leiden, The Netherlands.
Keywords: butterflies; skippers; Rhopalocera; Sulawesi; Wallace Line; distributions; biogeography;

hostplants.
All species and subspecies of butterflies recorded from Sulawesi and neighbouring islands (the Sulawesi
Region) are listed. Notes are added on their general distribution and hostplants. References are given to
key works dealing with particular genera or higher taxa, and to descriptions and illustrations of early
stages. As a first step to help with identification, coloured pictures are given of exemplar adults of
almost all genera. General information is given on geological and ecological features of the area. Combi-
ned with the distributional information in the list and the little phylogenetic information available, ende-
micity, links with surrounding areas and the evolution of the butterfly fauna are discussed.
Contents
Introduction ....................................................................................................................................................... 3
Acknowledgements ....................................................................................................................................... 5
Sulawesi and its place in the Malay Archipelago ............................................................................ 6
Biogeography of Sulawesi butterflies ................................................................................................. 14
Annotated checklist ..................................................................................................................................... 31
References ...................................................................................................................................................... 238
Index to butterfly names ......................................................................................................................... 256
Introduction
This paper presents an annotated checklist of the butterflies (Lepidoptera: Rho-

palocera) of the Sulawesi Region (see below), and was originally conceived in connec-
tion with the 1985 Royal Entomological Society of London Memorial Expedition Pro-
ject Wallace to Dumoga-Bone National Park, Sulawesi Utara. During this international
expedition, which extended over a full year, many members committed their field
notes on butterflies to large notebooks. These books, based on an illustrated version of
the original draft list that was made to aid field identifications, are deposited in The
1 Project Wallace Contribution 154.

4 Vane-Wright & de Jong. The butterflies of Sulawesi. Zool. Verh. Leiden 343 (2003)
Natural History Museum, London, and form an as yet largely untapped source of bio-
logical information. The information included in the present checklist is based primar-
ily on publications, personal experience and unpublished information received from
various colleagues. Museum collections have been checked only in cases of uncertain-
ty of identification, and the distributional information contained in collections has
only been used to a limited extent. The following abbreviations have been used:
BMNH – The Natural History Museum, London, ZSBS – Zoologische Sammlung des
Bayerischen Staates, München; other museums have been printed in full. The main
purpose of this checklist is to make the butterfly fauna of Sulawesi more accessible, so
that future students can more easily fill in the gaps. We remain hopeful that this work
will also form the starting point for production of a much-needed field-guide. Such a
guide would give an opportunity to include information from the Project Wallace field
notes.
Since the work on this checklist started, numerous publications have appeared that
directly or indirectly relate to the butterfly fauna of Sulawesi. We have tried to include
them all, but inevitably we will have missed some. Additions are most welcome. Also, the
classification to be adopted has had our special attention. There are widely different
classifications in use. For instance, the number of butterfly families recognised ranges
from five in Papilionoidea and Hesperioidea together (as in Ackery et al., 1999) to four-
teen in Papilionoidea only (as in d’Abrera, 2001). Little or no rational explanation can be
offered for such inconsistency, other than personal whim. We consider this an undesir-
able situation. If we do not take ourselves seriously, why should politicians and other
decision-makers do so? We are therefore strong supporters of the idea of an authorita-
tive standardized classification (e.g. Vane-Wright, in press b) – although we would not
agree with all of the proposals made by Godfray (2002). In this checklist we have fol-
lowed the as yet unpublished higher classification of the Global Butterfly Information
System (GloBIS: Lamas et al., 2000). GloBIS will eventually provide an updateable stan-
dard list world-wide, to be made available through the internet (Lamas et al., in prep.).
The current GloBIS higher classification is largely based on Ackery et al. (1999), the latest
comprehensive publication on the higher classification of butterflies, but also takes into
account a number of more recent works (e.g. Brower, 2000; Freitas & Brown, submitted).
Vernacular names in English have also been included. These are taken from a variety
of sources (e.g. Evans, Corbet & Pendlebury), and a few new ones have been coined
(e.g. Jordan’s Mormon for Papilio jordani, and Bedford-Russell’s Idea for Idea tambu-
sisiana). Lower case is used for common names applied to whole groups or genera
(e.g. awls), but the names are capitalised when they refer to a single species (e.g. Com-
mon Awl). Plant names largely follow Robinson et al. (2001).
The peculiar fauna of Sulawesi has attracted the attention of many collectors and
biogeographers, and continues to do so (e.g. Holloway, 2003). For a better under-
standing of the distribution and evolution of the fauna, exact knowledge of the distri-
bution of the species, their ecological requirements and phylogenetic relationships,
together with the geological history of the region, are all indispensable. We have used
available sources to assess the general distribution of the species. It would have been
beyond the scope of this paper to give exact localities on the island. We have restricted
ourselves to general indications like N, W, etc., as approximate estimations of the
known distributions across Sulawesi, and as a means to check whether the various
Vane-Wright & de Jong. The butterflies of Sulawesi. Zool. Verh. Leiden 343 (2003) 5
“arms” (peninsulas) of the island have faunas of their own. Although we have a gen-
eral idea of the ecological requirements of most species, such as “restricted to under-
storey of primary forest”, “only above 1500 m”, or “open shrubs”, our knowledge is
still too fragmentary to allow a correlation between ecological requirements and dis-
tribution. As a first step to a better understanding of ecological requirements we have
listed foodplants as far as known at present, and we give (but not exhaustively) litera-
ture references to published figures and descriptions of early stages (with these food-
plants and early stages usually being based on material from outside Sulawesi; data
are thus available for only a few of the endemic species).
Interest in the butterflies of SE Asia has been mainly descriptive: distributional
data, faunal surveys, description of early stages and new taxa. These studies have
brought a wealth of information. Little attention has, however, been given to phyloge-
netic systematics. This is disappointing, since the evaluation of phylogenetic relation-
ships gives a relative time frame for historical events. We have tried to assemble all
relevant information.
In recent years much progress has been made in reconstructing the complicated
geological history of the island. On the basis of recent geological information, the dis-
tributional information contained in the present checklist and, where available, phylo-
genetic analyses, our current understanding of the biogeography of the butterflies of
Sulawesi is reviewed.
Acknowledgements
As members of the Royal Entomological Society Project Wallace expedition, we

would particularly like to thank Bill Knight, the administrators of LIPI (Jakarta), and
the many expedition team members we worked with in Sulawesi in 1985 for making
this project a reality. We are grateful to the UK NERC Taxonomic Publications Grant
Programme, administered by the Linnean Society of London, for generous support in
defraying the costs of the coloured plates. We wish to thank Hideuki Chiba, Julie Har-
vey, Axel Hausmann, Jeremy Holloway, Lee and Jackie Miller, John Tennent, Andrew
Rawlins, Shen-Horn Yen and Gerardo Lamas for help with many taxonomic, biogeo-
graphical and bibliographical questions. Special thanks are also due to Phillip Ackery,
Alan Cassidy, John Eliot, Jane Goode, Djunijanti Peggie, Bob Smiles, Campbell Smith
and Osamu Yata. At various stages in the production of this work they made signifi-
cant contributions to its content. Formerly it was our intention to include many or
even all of them as co-authors. However, over the last eight or more years the list has
undergone innumerable changes due almost entirely to the input of RdJ and RIVW
(Osamu Yata contributed more recently with guidance on particular genera, notably
Appias). As none of our collaborators has had the opportunity to work on the numer-
ous iterations and revisions, or even sections of it, we have decided that authority
must rest with just the two of us: all errors of commission and omission are solely our
responsibility. The debt we owe to our colleagues is nonetheless considerable, and we
hope that inclusion of their names under the title goes some way to acknowledging
our special dues. Finally, we acknowledge Jeremy Holloway and Harish Gaonkar for
making numerous suggestions for improving and correcting the final manuscript,
many of which we have gratefully adopted.
Fig. 1. Sulawesi lies at the heart of the Malayan Archipelago. The pecked line encloses the Sulawesi
Region, the area covered in this publication.
Sulawesi and its place in the Malay Archipelago
Topography
Sulawesi, eleventh largest island in the world, lies almost literally at the heart of
the great Malay Archipelago (fig. 1). Immediately to its west is Borneo, the world’s
third largest island, four times the area of Sulawesi, the two being divided by about
120 km of open sea at the northern end of the Makassar Strait. To the north is Min-
danao, main island of the southern Philippines, a little over half the area of Sulawesi.
Although the two are separated by 400 km of the eastern Celebes Sea, an oceanic ridge
with scattered islands lies between. Notably, the Sangihe Archipelago occurs at the
half way point, and the largest uninterrupted sea gap in this whole chain is about 80
km (although many of the intermediate islands are very small). Some 700 km to the
east is New Guinea, largest tropical island in the world, well over four times Sulawesi
in area. Almost filling the Moluccan and Seram seas between the two, however, are
the extensive islands of northern and central Maluku (the “Moluccas”), as well as the
Banggai and Sula archipelagoes which together extend over 300 km to the east from
Sulawesi. As a result the largest uninterrupted sea gap between Sulawesi and New
Guinea is no more than 120 km. Approximately 600 km to the south-west lies Java,
two-thirds the size of Sulawesi and fifth largest island in the Archipelago. The unin-
terrupted distance between southern Sulawesi and eastern Java is probably no more
than 110 km, by way of the substantial Lesser Sunda islands of Flores, Sumbawa,
Lombok and Bali, and the many smaller islands of the Flores Sea.
Fig. 2. The Sulawesi Region. All names of islands of this region mentioned in this publication can be
found here, with the spelling adopted (mainly after Whitten et al., 2002). The thick lines are the
approximate boundaries of the areas used here; they do not coincide with provincial boundaries.
The Sulawesi Region

In addition to the main island of Sulawesi, the Sulawesi Region (sensu Vane-
Wright, 1991) covers the Sangihe and Talaud archipelagoes to the north, the Banggai
and Sula archipelagoes to the east, Buton and nearby islands, and the Tukangbesi
archipelago to the south east, and islands to the south including Salayar and Kalao
(fig. 2) 2. This is essentially the region described by Whitten et al. (1987, 2002), except
that Kep. Sula is politically part of Maluku province.
2 In the rest of the paper we shall use the Indonesian word kepulauan for archipelago, abbreviated to Kep.
Outline of present-day ecology

A detailed treatment of the ecology of Sulawesi, with extensive literature referen-
ces, is presented by Whitten et al. (1987, 2002). For the present purpose we are mainly
interested in surface relief, climate and vegetation.
Sulawesi is a mountainous island, reaching its highest point in the Latimojong
Mountains (Gunung Rantemario, 3440 m) in southern Torajaland (northern part of the
southwest arm), with a number of other peaks over 3000 m in C Sulawesi. Going
north, east and south the mountains are generally lower, but in the extreme south of
the southwest arm Gunung Lompobatang still reaches 2871 m, and peaks of over 2000
m are also found in the other arms. There are 10 volcanoes, mainly in the northeast tip
of the north arm and in the Sangihe Archipelago that have erupted in historical time.
In addition there are a number of mountains with volcanic activity, like fumaroles.
Extensive land below 1000 m is mainly found in the various arms and less so in the
central part of the island.
Rainfall is not evenly distributed over the island. In November-December cool
northwesterly winds bring moisture to the west coast, but the central part of this coast
is sheltered from these winds by Borneo. Around February humid winds blow from
the southeast. The eastern part of Sulawesi receives most rain between April and June.
When Australia cools down (winter) the southeasterly winds become stronger and
dryer, particularly influencing the climate on the southern tips, where the dry season
may last from April until November.
The general rainfall scheme is locally modified by mountain ranges. While Maros,
on the west side of the southwest arm, receives over 500 mm per month during the
rainy season, towns on the other side of the peninsula are in the rain shadow and
receive little. The effect of mountains is even more strongly expressed in the Palu Val-
ley, sheltered as it is by north-south mountain ridges. While the surroundings receive
2500-3000 mm rain per year (and the mountains even more), the Palu valley has an
annual rainfall of less than 600 mm.
In addition to altitude and climate, exposure, soil chemistry, soil quality and struc-
ture are important factors affecting the vegetation. Much of the eastern and southeas-
tern arms consist of ultramafic and mafic rocks, with Neogene and Quaternary sedi-
ments in large parts of the southeastern arm (and on the islands of Muna and Buton).
There is continental basement in the Banggai-Sula block and the opposite part of the
eastern arm, largely covered with carbonates. Much of the western part of the island
and the northern arm consists of Cenozoic volcanics and volcaniclastics, interspersed
with Tertiary sediments. Extensive areas of Quaternary sediments are found in the
central part of the southwestern arm, and along the west coast northwards. Tertiary
carbonates, once covered by volcanics, but exposed again due to erosion of the volca-
nic upper layer, are mainly found in the southern half of the southwestern arm and
locally in the northern part of the southwestern arm. One such area, east of Maros
(north of Makassar, for many years known as Ujung Pandang), is famous among col-
lectors for the numerous butterflies found along the river (fig. 5). Near the village of
Bantimurung the river empties from the Eocene and Miocene coral limestone hills
onto the plains. The locality is not only attractive to butterflies, it is also a popular
weekend resort for the people of Makassar who seek cooling in the river under the
waterfall. The waterfall is part of a nature reserve.
Fig. 3. Lowland forest along the Sungai Tumpah, Dumoga-Bone National Park, Sulawesi Utara, near
Project Wallace Base Camp, 225 m, 25th April 1985.
Fig. 4. Appias zarinda (left) and four species of Graphium (androcles, rhesus, eurypylus, anthedon) along
Sungai Tumpah, 225 m, Dumoga-Bone National Park, Sulawesi Utara, near Project Wallace Base
Camp, 10th May 1985.
Outline of present-day vegetation

The island must once have been almost entirely covered with lowland and monta-
ne primary rain forest, varying in composition according to soil type and variation in
rainfall (figs 3, 6-9). Forests on limestone mainly occur in the southwest and southeast
arms. Forests on ultrabasic soils are mainly found in the northern part of the southeast
arm. Much of central Sulawesi and the northern part of the southwest arm, stretches
in the north arm, and mountain ridges elsewhere, are clad in montane forest (figs 6-9).
In the southern part of the southeast arm, where the climate is more pronouncedly
seasonal, lowland monsoon forest occurs. Much of the lowland forest, particularly in
areas with high population pressure like the southwest arm, the southern part of the
southeast arm and the tip of the north arm, is disturbed, degraded, or completely
gone. The disturbance may go quite high into the mountains. Around West Toraja, for
instance, hardly any forest is left up to 1600 m (fig. 8). A number of rather extensive
forest areas are protected, like Dumoga-Bone in the north arm (the main site of Project
Wallace; fig. 3), Lore Lindu in the central part, and Morowali at the base of the eastern
arm (see Collins et al., 1991: map 19.5).
Although not contributing much to the butterfly fauna, large stretches of inland
swamp must be mentioned. They are mainly found near the west coast of Central
Sulawesi, and in the north and the south of the southeast arm. The last area, the
Aopa swamp, about 100 km west of Kendari, is the only major area of peat swamp
in Sulawesi. It forms part of the Rawa Aopa-Watumohae National Park. Another
type of vegetation that does not contribute much to the butterfly fauna is mangrove
(although populations of the very variable species Danaus affinis should be sought
there). Most mangrove is found along the northern part of the Bone Bay (between
the southwest and southeast arms) and along the coast of the southeast arm. Most of
the west and north coast of Sulawesi is devoid of mangrove vegetation.
Outline of geological evolution

The region is of very great interest to geologists, and access to much of the older
geological literature, together with valuable accounts of current ideas on the geolo-
gical history of the area, can be found in Hall & Blundell (1996), Hall & Holloway
(1998) and Hall (2002). A good review of recent findings and conclusions with
regard to Sulawesi was presented by Moss & Wilson (1998). Sulawesi originated
from a number of tectonic provinces that during the Cretaceous and Tertiary accre-
ted onto Sundaland. The following areas will be discussed: west, central, and part of
southeast Sulawesi; east and part of southeast Sulawesi; north Sulawesi; south Sula-
wesi; Banggai-Sula block; Buton-Tukangbesi block. In addition, a few words will be
said on the evolution of the Moluccas and the Philippines, since these islands may
have played a part in the colonisation of Sulawesi (cf. Mey, 2003).
By the late Cretaceous west Sulawesi had been accreted to Borneo and there was
continuous land. West, central, and parts of the SE arm of Sulawesi are thought to
have formed a contiguous land area during the early Paleogene, and at least west
Sulawesi, connected to Borneo, appears to have been emergent up to the early Eoce-
ne. In the middle of the Eocene, approximately 42 Ma, the land connection between
Borneo and Sulawesi was severed and the Makassar Strait formed. Much of the land
of proto-Sulawesi disappeared below sea-level, and only a number of small islands
may have been in existence until the middle Miocene. There was, however, a volca-
nic arc, part of which may have been emergent, extending down the east side of
western Sulawesi into southern Java. Probably land areas became emergent in centr-
al Sulawesi as a result of the late Oligocene collision of the east and part of southeast
arm onto west Sulawesi. In late Miocene and Pliocene there were extensive low
lying land areas in west, central and east Sulawesi. Pliocene collisions and subduc-
tion east of Sulawesi resulted in uplift of extensive areas in Sulawesi, and rapid
uplift of high mountain areas, particularly in central Sulawesi.
The east arm and part of the southeast arm, drifting from the edge of the Austra-
lian plate, remained submerged until after they had accreted onto Sulawesi in late
Oligocene (ca 18 Ma). Since Miocene times (ca 20 Ma) there has been extensive low
lying stretches of emergent land.
The north arm is composed of thick Tertiary sedimentary and volcanic deposits.
There was a volcanic arc in Miocene and Pliocene, related to the south-dipping sub-
duction of the Celebes Sea oceanic crust under the north arm. Some of the volcanoes
may have been emergent. The Quaternary to Recent arc of active volcanoes running
from the eastern part of the north arm through the Sangihe Islands, is related to west-
dipping subduction under this area. During the early Pliocene most of the north arm
was submerged. Similarly, the south arm was below sea level for much of the Tertia-
ry, except for emergent volcanoes. Probably only in the Pliocene did the island areas
of the south arm become connected with the land area in central Sulawesi.
During the Miocene or earliest Pliocene two microcontinental blocks, Banggai-
Sula and Buton-Tukangbesi, accreted onto east Sulawesi, undoubtedly resulting in
the formation of emergent land areas. These blocks rifted from the margins of the
Australian continent in the late Mesozoic. After rifting they submerged and only
became emergent in the Tertiary. Consequently, no Australian fauna or flora could
have been rafted on these microcontinental blocks. On the other hand, the emergen-
ce of areas of dry land between Sulawesi and the steadily northwards-drifting Aus-
tralian continent may have facilitated island hopping.
Similarly, although there was no dry land between Sulawesi and the coast of
Australia-New Guinea before the Miocene emergence (Audley-Charles, 1986, 1993),
the emergence of (part of) the Moluccas must have made the distance between Sula-
wesi and New Guinea considerably shorter. Fortuin & de Smet (1991) estimate the
time of emergence of Seram at 5 Ma, and a similar figure may apply to other islands
of the Moluccas. Halmahera in the northern Moluccas, however, itself of composite
origin, has a very different history (for a summary, see Hall et al., 1995). It was part
of an island arc that also comprised the east Philippine islands, as well as Waigeo,
Biak, Yapen and parts of present-day northern New Guinea. At 10 Ma Halmahera
still lay approximately 800 km southeast of its present position (Rangin et al., 1990).
Probably it was mainly submerged for much of its life. The younger, volcanic wes-
tern part and the much older (Cretaceous or older) eastern part collided only
between 3 and 1 Ma. The island reached its present position only recently and is still
moving westward. Thus it has never been closer to Sulawesi than nowadays, and
faunal exchange has never been so easy. However, there is still a relatively long
stretch of sea between the islands.
Not only the Philippine archipelago as a whole, but also several of its compo-
Fig. 5. Gate to the Bantimurung waterfall, near Maros, Sulawesi Selatan, 50 m, 10th June 1985. In later
years the butterfly gate was replaced by a gate with a huge monkey, but the butterflies still abound
along the water.
Fig. 6. Lower montane forest in Dumoga-Bone National Park, Sulawesi Utara, Edward’s subcamp,
Project Wallace, 780 m, 30th April 1985.
Fig. 7. View from top of Gunung Sampapolulu, 1590 m, Pulau Kabaena, Sulawesi Tenggara, 3rd
November 1989; monsoon forest and natural grassland.
Fig. 8. Practically all forest up to c. 1600 m has been cleared in West Toraja; vicinity of Mamasa, 1650
m, Sulawesi Selatan, 10th April 1991.
nent islands (including Mindanao, the main Philippine island closest to Sulawesi)
are of a composite nature (Rammlmair, 1993; Hall, 1998). Much of the eastern
islands once belonged to an island arc of which Halmahera and, at an earlier stage,
the north arm of Sulawesi also formed parts. Although there must have been areas
of dry land (e.g. emergent volcanoes), their extent is unclear and it seems unlikely
that possible similarities between the faunas of Sulawesi, Halmahera and the Philip-
pines are due to their once having belonged to the same island arc. We are of the
opinion that butterfly exchange between Sulawesi and the Philippines has been lar-
gely dependent on the dispersive powers of the insects. Substantial exchange (which
may still be going on) only became possible in the Pliocene, when north Sulawesi
emerged from the sea and the Philippine islands reached their present position.
The repeated drop in sea level during the Pleistocene as a consequence of glacia-
tions in the northern hemisphere did not bring the Moluccas or the Philippines much
closer to Sulawesi, but the southeastern coast-line of Borneo extended considerably
eastward to Sulawesi. Even during the last 17000 years sea level was 100 m below pre-
sent level for about 4000 years (Voris, 2000), bringing Borneo within about 50 km from
Sulawesi. Based on distance alone faunal exchange between these islands cannot have
been more difficult than between Sulawesi and the Moluccas or the Philippines.
Biogeography of Sulawesi butterflies
Ever since Alfred Russel Wallace (in a letter to Henry Bates in 1858, and in a series
of later publications) proposed the idea of a line (the so-called Wallace Line, Huxley,
1868) dividing the Asian and Australian faunas, the region has been of exceptional
interest to biogeographers (for reviews, see Whitmore, 1981, 1987; Holloway, 1997;
Turner et al., 2001). Wallace’s views on the exact position of the line changed with
time, from between Borneo and Sulawesi (Celebes) to east of Sulawesi. This had to do
with the enigmatic nature of the fauna of Sulawesi. Later authors proposed still other
demarcation lines, depending on the group of animals studied. The easternmost of
these lines (Lydekker’s Line and part of Weber’s Line) followed the 180 m line of the
Sahul shelf between New Guinea and the Moluccas, while the original Wallace Line to
the west of Sulawesi more or less followed the 180 m line of the Sunda shelf. Debate
and discussion of these supposed lines continues to this day (e.g. Atkins et al., 2001)
but, as Williams et al. (1999) have demonstrated for African birds, it is not realistic to
look for simple “lines”, but rather investigate transitions in terms of species richness
and species turnover (cf. Holloway & Jardine, 1968). Such methods have yet to be
applied to the Malay Archipelago.
The sea between the Sunda shelf and the Sahul shelf is deep. The islands in this
area were called Wallacea by Dickerson (1928), suggesting that they have much in
common, but actually the faunas of the included islands may differ considerably, par-
ticularly on Sulawesi, where endemism is high.
The first major account of the butterflies of Sulawesi was in a series of papers by
Martin (1914-1920, 1920-1924, 1929; see also Röber, 1940). The biogeography of Sula-
wesi butterflies has been discussed by a number of authors, including Toxopeus
(1930), Röber (1940), Holloway & Jardine (1968), de Jong (1990), Vane-Wright (1991),
Holloway (1991, 2003) and Vane-Wright & Peggie (1994). See also Otsuka (1996), who
concludes that there is almost no influence of Sulawesi on the butterflies of Borneo.

The composition and distribution of the butterfly fauna of Sulawesi were discus-
sed at length by Vane-Wright (1991) in relation to the known or assumed geological
evolution of the area. He concluded that “the original terrestrial biota of Sulawesi was
Asian, and that collision with the Australian Plate 15 [Ma] brought few (if any) Austr-
alian Region butterflies directly to Sulawesi.” and a “significant increase in the land
area of Sulawesi over the last 15 [Ma] could offer an explanation for the island’s relati-
vely low number of species.” To reach these conclusions he analysed the links
between the butterfly faunas of Sulawesi and surrounding islands at species and
genus level, and also used the few relevant cladistic analyses available. While general-
ly still supporting these conclusions, we present an update of the analysis.
As already described, Sulawesi is a composite island that originated from the
accretion of several land areas which were islands since the early Tertiary. It implies
that most, if not all, butterflies on Sulawesi are progeny of species that crossed water
gaps. Success of colonization is dependent on finding the right habitat and, most
importantly for Lepidoptera, the right foodplants. Apart from geological evolution,
ecological evolution must have played a major role in the distribution of the butter-
flies. Similarly, present-day ecology is important in the distribution within the island.
Unfortunately, as stated above, the ecological requirements of most of the species are
poorly known in detail. There is some general knowledge of foodplants and broad
habitat preferences (like open grassy areas, open forest, closed forest, etc.), but altitu-
dinal ranges, for instance, are poorly documented. This lack of knowledge hampers
the analysis of a possible correlation between distribution and ecology.
High endemism, low richness: basic puzzle of the Sulawesi butterfly fauna
All of the major islands and island groups surrounding Sulawesi, together with a few
others such as Palawan (850 km to the nor-nor-west), are areas of endemism. Given the
central position of Sulawesi, it is surprising that its butterfly fauna is relatively more
endemic than any of the immediately surrounding islands. Equally, given its large size as
well as centrality, the smaller absolute size of its butterfly fauna in comparison to the
smaller and seemingly peripheral islands of Mindanao and Java is also surprising. Note-
worthy also is the comparison with Borneo: only 120 km away, it has more than twice the
number of butterfly species found on Sulawesi, a magnitude of difference not readily
explicable by its greater size alone. The basic figures per family are given in table 1.
Table 1. Number of endemic and non-endemic species in the Sulawesi Region per family. SR = ende-
mic to (some part of ) the Sulawesi Region, Sul = restricted to the island of Sulawesi, si = restricted to
satellite islands.
total non-end SR Sul si

Hesperiidae 187 163 124 115 10
Papilionidae 140 125 115 117 14
Pieridae 152 126 126 114 14
Lycaenidae 183 106 177 150 11
Riodinidae 114 114 10 110 10
Nymphalidae 191 194 197 147 19
total 557 318 239 133 28

Fig. 9. Montane forest at top of Gunung Muajat, 1780 m, east of Kotamobagu, Sulawesi Utara, 31st
May 1985.
Non-endemic faunal elements
As noted above, Vane-Wright (1991), based on the original version of this checklist
prepared for Project Wallace, analysed the distribution patterns of the non-endemic
Sulawesi butterfly fauna in an attempt to understand this problem. He enumerated
and tabulated the Sulawesi species and genera shared with seven surrounding areas
of endemism, singly and in any of the 120 possible combinations of these areas. Those
taxa found in all seven surrounding areas were considered uninformative, as were the
endemic taxa, which can only be made informative in the light of cladistic analyses (as
already indicated, still lacking for more than a fraction of the taxa). Vane-Wright con-
cluded that two general patterns could be observed. First, an ‘older’ pattern, based on
the analysis of genera, which linked Sulawesi to Asia, but with no special links to Bor-
neo. Not a single, currently recognised butterfly genus is restricted to Sulawesi + Bor-
neo – although the rare and rather widespread Artipe appears to hold that distinction
when looking at just the seven areas and Sulawesi. Second, a set of ‘younger’ patterns,
based on the analysis of non-endemic species, links Sulawesi to Maluku, the Philippi-
nes and the Lesser Sunda islands, in addition to the Asian pattern, also strongly evi-
dent in the species distributions. Of these so-called younger patterns, Vane-Wright
(1991) concluded that the link to the Moluccas was the “most pronounced.”
Faunal analysis revisited

Since 1991, the number of species recorded in our Sulawesi list has increased
modestly, from 470 to 488 for the island of Sulawesi only (to 557 for the Sulawesi
Region), and the number of genera likewise, from 183 to 191 (194 for the Sulawesi
Region). Some of these changes are due to new discoveries, others to changing taxo-
nomy. However, in terms of the distribution of non-endemics, other changes also
involve refinement in our documentation and knowledge of the surrounding areas,
and in particular the fauna of northern and central Maluku. Vane-Wright & Peggie
(1994) demonstrated that these two areas were indeed separate areas of endemism,
and that Obi (treated as “ambiguous” by Vane-Wright, 1991) clearly belonged, on the
basis of its faunal composition, to northern Maluku. Their work depended on still lar-
gely unpublished lists (Peggie et al., 1995, is the exception) documenting the entire
Maluku butterfly fauna, and we have drawn on these compilations to refine our esti-
mates of the ranges of the non-endemic Sulawesi genera and species. The publications
of Seki et al. (1991), Corbet & Pendlebury (1992), de Jong & Treadaway (1993c), Tre-
adaway (1995), and Parsons (1999) have also been of great help in this general faunal
documentation, together with a host of scattered papers by many different authors,
often dealing with discoveries of individual new populations and subspecies.
Although quite a lot of details have thus changed, and the tabulated numbers and
percentages now differ as a result, the overall conclusions of Vane-Wright (1991)
remain broadly valid – at least, in terms of any analysis along the same lines. Rather
than duplicate the entire discussion and argumentation presented in Vane-Wright
(1991), we present here just the basic information about the areas used in the analyses,
together with four tables: one for genera and one for species, corresponding to tables 2
and 3 in Vane-Wright (1991), a third concerning within-Sulawesi distributions, and a
fourth dealing with endemism. Given the descriptive distributional account presented
for each taxon, together with the codes indicating distribution in the seven surroun-
ding areas, all the data are explicit in the checklist, and available to anyone who might
wish to make their own analyses.
The areas and codes

Sulawesi is defined here as the main island bounded by its sea shore.
(E) Known distribution entirely within the island. Butterfly taxa found widely but
apparently never beyond the shoreline include Aoa, Bletogona, and the subgenus
Pseudamathusia.
Sulawesi Region includes numerous offshore islands, extending to Talaud to the
north, Sula to the east, Buton, Tukangbesi to the south-east, and Salayar, Tanah-
jampea, Kalao and other islands to the south (fig. 2).
(R) Taxon with known distribution entirely bounded by the Sulawesi Region, inclu-
ding records for at least one of its off-shore islands in addition to confirmation for
the main island. Such regional endemics include Lohora, Papilio gigon and Neptis ida.
(L) Taxon with distribution bounded by Sulawesi Region, but no records from the
main island. Such local endemics include Troides dohertyi, found only in the Sangi-
he and Talaud archipelagos.
(P) Taxon occurring both within and beyond the Sulawesi Region, but without any
records from the main island. Such peripheral butterflies include Papilio rumanzo-
via, likewise found in Sangihe and Talaud, but also beyond, in the Philippines.
(1) Palawan. Palawan island and its close “satellites”. Endemics include Trogonoptera
trojana and Elymnias parce.
(2) Mindanao. The southern Philippines: Mindanao, Basilan, Bohol, Leyte and Samar.
Endemics include Papilio antonio and Discophora philippina.
(3) Northern Maluku (as defined by Vane-Wright & Peggie, 1994). Halmahera, Moro-
tai, Ternate, Batjan and Obi. Hypochrysops siren is endemic to this area.
(4) Central Maluku (as defined by Vane-Wright & Peggie, 1994). Buru, Seram,
Ambon, Saparua and various smaller islands. Delias dorimene and Hypolimnas pan-
darus are among those species restricted to this area.
(5) Lesser Sunda Islands (with Bali as ambiguous). The great chain of small islands,
from Bali and Lombok east through Flores to Timor and Tanimbar. Endemics to
this area include Melanitis belinda and Delias sambawana.
(6) Java (with Bali as ambiguous). Java, Bali and some minor offshore islands. Species
restricted to this area include Ypthima nigricans and Cyrestis lutea.
(7) Borneo. The main islands and its close “satellites”, including Laut. Endemics
include Troides andromache and Chersonesia excellens.
Combination codes are used to specify the distribution of Sulawesi taxa on two
or more of the seven surrounding islands or island groups. Thus, if there were a
butterfly known only from Sulawesi, Palawan and Flores, it would be coded (1+5).
No such taxon has been found - and indeed, of the 120 possible combinations invol-
ving 2, 3, 4, 5, 6 or 7 islands at a time, less than half (52) are supported by empirical
evidence and, of these, no less than 19 are represented by just single examples. The
most common combinatorial pattern of all involves all of the surrounding islands
(1+2+3+4+5+6+7), coded more simply as widespread (W) in the checklist: a total of
Table 2. Principal, repeated, potentially informative distribution patterns amongst non-endemic but-
terfly genera found on Sulawesi (all totally widespread and Sulawesi Region endemic genera exclu-
ded, together with patterns exhibited by only one genus). The eight repeated patterns not tabulated
here were supported by just two or three examples each. The top 4 of the 14 repeated patterns account
for 65% of the 89 genera covered by the table, and represent all of the surrounding areas except nort-
hern and central Maluku. This is the ‘older’, Asian pattern discussed in the text.
The coded areas are 1: Palawan, 2: Mindanao region, 3: northern Maluku, 4: central Maluku, 5: Lesser
Sunda Islands, 6: Java, 7: Borneo.
pattern percent no. of examples

1+2+3+4+5+6+7 28.1% (25)
1+2+3+4+5+6+7 20.2% (18)
1+2+3+4+5+6+7 9.0% (8)
1+2+3+4+5+6+7 7.9% (7)
1+2+3+4+5+6+7 6.7% (6)
1+2+3+4+5+6+7 5.6% (5)
Eight others 22.5% (20)
100.0% (89)
Table 3. The ten most strongly supported biogeographic patterns shown by native, non-endemic
Sulawesi butterfly species, as subsets of the seven surrounding areas of endemism. Endemic, perip-
heral and totally widespread species have been disregarded. Two major classes of these ‘younger’
patterns are evident: Asian links involving combinations of areas 1, 2, 5, 6 and 7, very similar to those
seen in the generic analysis, and an eastern linking of Sulawesi with the Moluccas. Components lin-
king to the north (Mindanao) and to the south (Lesser Sundas + Java) are also apparent, and are
stronger than any pattern linking exclusively to Borneo (just five species exhibit this pattern, not
shown here as it lies outside this ‘top ten’).
For area codes, see table 2.
pattern percent no. of examples

1+2+3+4+5+6+7 7.4% (8)
1+2+3+4+5+6+7 10.1% (11)
1+2+3+4+5+6+7 12.0% (13)
1+2+3+4+5+6+7 11.1% (12)
1+2+3+4+5+6+7 7.4% (8)
1+2+3+4+5+6+7 7.4% (8)
1+2+3+4+5+6+7 17.6% (19)
1+2+3+4+5+6+7 2.7% (3)
1+2+3+4+5+6+7 19.4% (21)
1+2+3+4+5+6+7 3.7% (4)
100.0% (107)
130 genera and species found on Sulawesi show this uninformative pattern. The
second most common pattern involves five areas (1+2+5+6+7); a total of 45 species
and genera found on Sulawesi have this pattern, equivalent to widespread other
than in N and C Maluku. The distributions of all but one of the total of 751 genera
and species recorded here from the Sulawesi Region can be encoded by this system -
the distinctive nymphalid genus Pseudergolis being the lone exception. Represented
on Sulawesi by a single endemic species, this disjunct genus is not recorded from
any of the surrounding islands, but recurs only on the Asian mainland; in our list
this single exception is coded (D). Finally, it should be noted that a few species are
listed that are considered very uncertain with respect to their genuine presence in
Sulawesi, and no distribution code is given for any of these. Likewise, if a species is
known, for example, from Sulawesi, Borneo and Java, but only tentatively for the
Lesser Sundas, it is coded as (6+7), not (5+6+7), nor even (5?+6+7).
Are there distributional patterns on Sulawesi itself?

In the checklist the distribution over the island of Sulawesi has been very rough-
ly indicated by N, C, S, E and SE (not exactly coinciding with the four administrati-
ve provinces). The inventory is far from exhaustive. In particular, the east and sou-
theast arms are underrepresented: published records are much scarcer than for the
other parts, and some good collections from these areas still await working up. Even
so, if we only take the species in N, C and S into account, a remarkable pattern is
evident (Table 4). Of the 356 non-endemic species on Sulawesi, similar numbers of
species occur in N, C and S (columns 8-10 in Table 4). However, if we break these
numbers down according to their distributional width, the distribution is not as
even as it may seem. Supposing that a non-endemic species occurring in N and S,
but not known from C, has been overlooked in C, the number of species widespread
on Sulawesi is 246 (70%). Disregarding the few non-endemics that for unclear reas-
ons are restricted to C (perhaps overlooked in N and S, or with narrow ecological
tolerance), we find that the number of species restricted to N (24) and to N+C (27)
together make up 14.3% of the non-endemics, while the number of species restricted
to S (34) and to C+S (15) together make up 13.8% of the non-endemics. Far fewer
species are restricted to C, and the total number in C (52, or 14.6%: 42 N+C and S+C,
plus 10 restricted to C) is only so high because of overlap of N+C and S+C. In other
words, the non-widespread non-endemics show peaks in N and S. Considering that
the butterfly fauna on Sulawesi is the result of immigration, these figures suggest
that the non-endemics restricted to the northern or southern parts of Sulawesi are
later arrivals (from the Philippines and Java/Lesser Sunda Islands, respectively; a
historical explanation) or slower dispersers (an ecological explanation) than the non-
endemics which are widespread on Sulawesi. Moreover, the higher number of spe-
cies restricted to N+C than to S+C may point to an easier dispersal from N to C than
from S to C, that is to say, barriers between N and C are less severe than between S
and C.
The within-island distribution of endemic taxa will be discussed below.
Table 4. Distribution of non-endemic and endemic species over N, C and S Sulawesi (E and SE have
been disregarded, see text). The numbers in the first seven columns (N to N+C+S) refer to species res-
tricted to the marked areas. In this table, endemic species are species restricted to the island of Sulawe-
si only; all other species on Sulawesi also occurring on other islands, even when restricted to islands of
the Sulawesi Region, have been considered non-endemic.
N C S N+C N+S C+S N+C+S N total C total S total

total 38 50 50 47 17 23 263 365 383 353
non-end (Sul) 24 10 34 27 16 15 230 297 282 295
end (Sul) 24 40 16 20 1 8 33 68 101 58
Endemism, and Sulawesi as a critical island fauna
Generic level endemism

As yet we do not have sufficient collated data available to evaluate Sulawesi
Region generic endemism in relation to other parts of the Malay Archipelago, but at
3.6% it appears to be modest (cf. genus level endemism for New Guinea calculated at
14.8% by Parsons, 1999: 33). The significance of this Sulawesi endemism is uncertain.
Six of the seven genera involved have only one (Ilma, Aoa, Nirvanopsis, Lamasia) or two
included species (Bletogona, Uranobothria). The exception is Lohora (Satyrinae: Mycale-
sina), with 17 species currently recognised. Unlike most mycalesines, however, the
species of Lohora are difficult to separate by their male genitalia, and the status of
several remains doubtful (Vane-Wright & Fermon, in press). Moreover, the characters
by which Lohora is separated from Mycalesis, other than certain constant modifications
to the wing-pattern and venation groundplan, are not clear to us. This suggests the
possibility that Lohora represents an internal subgroup of Mycalesis that has undergo-
ne recent radiation in the Sulawesi Region. The genus would make an excellent sub-
ject for investigation by molecular systematics.
Species endemism: Sulawesi as a critical island fauna

Species level endemism in the Sulawesi Region exceeds 40%. This is very high
compared to the Malay Peninsula (2%: Corbet & Pendlebury, 1992). It is also high in
comparison to most of the surrounding islands, with the exception of the collective
Philippine islands proper (Philippines minus Palawan group), which approach the
same level (Treadaway, 1995; de Jong & Treadaway, 1993c; Vane-Wright, 1990; Vane-
Wright & Peggie, 1994), and the very much larger island of New Guinea (46%, rising
to 55% if satellite islands are included: Parsons, 1999: 22-23). For northern and central
Maluku, Vane-Wright & Peggie (1994) documented levels of butterfly species ende-
mism at about 11% and 15% respectively. Species endemism for the western Lesser
Sundas, Java, Borneo and Palawan is, in each case, probably no more than about 10%,
but the relevant data have yet to be collated. Although all these values pale in compa-
rison to Madagascar (70-74% species endemism: Lees et al., in press), a value of over
40% for a land area or even island the size of Sulawesi is nonetheless impressive.
Notably, the Danaina plus Euploeina (Danaini) of the Sulawesi Region include 15
endemics out of a total of 38 species, making this the richest and most specialised
fauna for milkweed butterflies in the world. This observation, plus the personal expe-
rience of the present authors of the ecological destruction of the neighbouring central
Philippines, led Ackery & Vane-Wright (1984) to explore the idea of minimum sets of
local faunas across the world that could represent all species of a particular group.
The procedure they proposed, “critical faunas analysis”, depended heavily on a
knowledge of endemism. Collins & Morris (1985) applied this method to the Papilion-
idae, and as a result also recognised Sulawesi as an outstanding critical fauna for glo-
bal conservation needs.
Table 5. Endemism among butterfly genera and species found in Sulawesi Region, and on Sulawesi.
Total genera found in Sulawesi Region 194

Total genera on Sulawesi 191
Total genera unique to Sulawesi Region 7
Total genera unique to Sulawesi 5
Total species known from Sulawesi Region (a) 557
Total species known from Sulawesi (b) 488
Total species unique to Sulawesi Region (c) 239
Total species unique to Sulawesi 133
Total spp. endemic to Region not on main island (d) 28
Total number of non-endemic, peripheral species 43
Percentage endemic spp. in Sulawesi Region (c/a x 100) 42.9%
Percentage endemics on Sulawesi (c-d/b x 100) 43.2%
Although the unsophisticated procedures adopted in such analyses have now

been entirely superseded by methods based on assessing data for near equal-areas
using complementarity (Williams, 2001), incorporating for practical conservation eva-
luation a far wider range of factors (Margules & Pressey, 2000; Williams & Araújo,
2000; Araújo et al. 2002), the present simple analysis of relative and absolute levels of
endemism nevertheless underlines the significance of Sulawesi as a critical fauna. If
all the native butterflies of the Sulawesi Region became extinct, the world would lose
more than one in a hundred of all known butterfly species. Currently there is a very
real danger of this happening to the equally significant fauna of the Philippines. Habi-
tat destruction in Sulawesi is less advanced, but seems to be continuing, and at an
alarming pace (M.F. Kinnaird and T.G. O’Brien, in Whitten et al., 2002: xiv-xx).
Is the Sulawesi Region an area of endemism?

Vicariance biogeography relies heavily on the idea of “areas of endemism” to pro-
vide units for analysis. The definition of an area of endemism is, however, not precise.
Vane-Wright & Peggie (1994) explored a simple “test” based on the expectation that,
on incrementally increasing land area sub-sampled within an area of endemism, per-
centage endemism should rise (tending to zero as sampled area tends to zero, and ten-
ding to 100% on approaching continental and global scales). If, as a result of adding a
particular area, percentage endemism falls (or at the limit remains the same), then it is
likely that a boundary has been transgressed, and that two or more incomplete and
separate areas of endemism are being conflated. For example, Vane-Wright & Peggie
(op. cit.) found that on adding faunal data for Obi to data for Morotai, Bacan, Halma-
hera and Ternate in northern Maluku, percentage endemism for the combined area
almost doubled. In contrast, on adding the Obi data to that for Buru, Seram and
Ambon in central Maluku, percentage endemism fell from 15% to 14%. From this they
concluded that Obi belonged to an area of endemism they termed N Maluku, and not
to C Maluku. On combining the data for N and C Maluku, percentage endemism
increased to 21% (although, for other reasons, Vane-Wright & Peggie concluded that
the two areas taken together did not form “a well-marked” area of endemism).
On adding data for all the peripheral islands included here as part of the “Sulawe-
si Region”, it is notable that percentage species endemism drops slightly (Table 5).
This suggests that, although convenient for the purposes of our checklist, the Sulawesi
Region as defined here is not a fully coherent area of endemism. Further work is nee-
ded to establish the natural limit of the Sulawesi endemic area. Almost certainly it will
be found that, for example, inclusion of data for close island and island groups like
Muna and Kep. Banggai will increase total percentage endemism, whereas more
remote islands and island groups such as Kalao and Kep. Talaud will reduce it (as
they almost certainly sample the fauna of the western Lesser Sunda and Mindanao
regions, respectively, to which they most probably “belong”). In order to make any
such tests, comprehensive data sets for all the surrounding islands and areas are nee-
ded. Regrettably, we do not yet have the relevant data fully collated.
Are there distribution patterns in the endemics of Sulawesi?

The endemics of Sulawesi show a very different distribution pattern from the non-
endemics (Table 4). The number of widespread endemics (i.e. occurring in N and C
and S - a total of 32) is only 25% of the total number of endemics, quite different from
the 70% of widespread non-endemics. Comparing the total number of endemics in N,
C and S (Table 4 columns 8-10) it becomes already apparent that C, with ca 76% of the
endemics, is richest, but it is even more apparent if we break the numbers down into
smaller areas. Of the species restricted to either N, C or S (70 in total), 57% (40) are
found in C. Of the 98 species restricted to one area or two adjoining areas, 85.7% are
restricted to N and/or C. In other words, C is richest in endemics in general and in
narrow endemics in particular and, similarly to the situation with non-endemics, the
barrier between N and C appears less severe than between C and S. The reason for
this is not clear. There may be better opportunities for speciation in C, or C may have
had a longer subaerial life.
Celebes forewing and gigantism: other manifestations of endemism?

In some parts of the world, notably areas of the tropics, many un-related butterfly
species share a particular facies. Almost all such cases are caused by mimicry: conver-
gence to form “rings” of aposematic and pseudaposematic species all locally similar in
appearance, such as the well-known glasswings and their mimics in the neotropics, or
Amauris and its look-alikes in Africa. In contrast, the butterflies of Sulawesi are unique
in that quite unrelated species show apparent convergence in size and wing shape,
seemingly unconnected with mimicry. These phenomena, known as “Celebes fore-
wing” and “gigantism”, were first noticed and commented upon by Wallace (1865,
1867, 1869). Celebes or Sulawesi forewing involves either extreme acumination of the
forewing tip (well seen in Appias zarinda), and/or a pronounced bending of the fore-
wing costa (as in Idea tambusisiana), in comparison to related species (e.g. Appias nero,
Idea blanchardii). Gigantism refers to the observation that Sulawesi butterfly species are
often larger than corresponding subspecies or their close relatives in surrounding
areas. Good examples include Papilio peranthus (the Sulawesi race is far larger than the
other populations of this species or complex, found in Java and the Lesser Sundas)
and Zethera incerta (spectacularly large for a satyrid, and much larger than any of the
other five species of the genus, all of which are confined to the Philippines).
Wallace described these parallelisms only among Papilionidae, Pieridae and
Nymphalidae, but they are more widespread, also commonly occurring in Lycaeni-
dae (Toxopeus, 1930). Moreover, in many Lycaenidae there are parallel shifts in
sarpedon group Oriental & Australian Regions

aricles Burma to Sundaland, Palawan
meyeri Sulawesi endemic
leechi China
bathycles Sundaland
chiron continental Asia
doson West of Wallace’s Line
procles N Borneo
evemon SE Asia to Sundaland
euryples NE India to Australia
Fig. 10. Species and area cladogram of the Graphium eurypylus group, after Saigusa et al. (1982). Taxa
occurring in the Sulawesi Region have been printed in bold.
wing markings (widening of dark margin on upperside of forewings in females;

stronger discoidal stripe on upper and underside; expansion of eyespots, and their
colour intensified; tornal spot on the underside of the hindwing with orange lunule
strongly reduced, but with expanded white or pale blue distal line). Although these
phenomena have yet to be investigated in a quantitative, rigorous manner, casual
observations suggest they are real. Even though their origins and biological signifi-
cance remain mysterious, they appear to be further manifestations of the endemism
and peculiarity of the Sulawesi fauna.
Cladistic analysis
Application of phylogenetic information to biogeographic analysis renders endemic

species informative, by placing them in a broader context through recognition of their
sister taxa, and thereby establishing their place in the evolution of the monophyletic
group to which they belong. This makes it possible to set historical events in a chronolo-
gical order. Unfortunately there are not many useful phylogenetic analyses available for
endemic Sulawesi butterflies. The available information is summarized here.
Graphium meyeri is a Sulawesi endemic belonging to the G. eurypylus group. In the
phylogenetic tree for all nine species proposed by Saigusa et al. (1982) it occupies the
most basal position but one (fig. 10). All other species are confined to the areas to the
subgenus Hestia Sri Lanka, S India to Sundaland

tambusisiana Sulawesi endemic
leuconoe Thailand, Sundaland, Phil., Taiwan
hypermnestra Thailand, Sundaland
electra Philippines
blanchardii Sulawesi Region endemic
durvillei N Moluccas, New Guinea
idea S Moluccas
Fig. 11. Species and area cladogram of Idea (Idea), after Kitching et al. (1987) and Vane-Wright (1991).
Species occurring in the Sulawesi Region have been printed in bold.
pumila group Papuan Region

crowleyi group Indo-sundaland to Flores
Philippines, Sulawesi
menadensis Sulawesi Region endemic
tityoides Sumatra
pseudomelaneus Java
albata Sumatra, Java, Bali
timorica Timor endemic
hypowattan Sulawesi endemic
dabrerai Sulawesi endemic
toxopei Sulawesi endemic
kuekenthali Sulawesi endemic
Fig. 12. Species and area cladogram of a clade of Parantica, after Ackery & Vane-Wright (1984). Species
occurring in the Sulawesi Region have been printed in bold. According to Morishita (1985), tityoides is
a subspecies of pseudomelaneus.
west and north of Sulawesi, except the crown species G. eurypylus, which extends from
India to Australia. This strongly suggests an Asian origin of G. meyeri, at a relatively
early date. After its separation, seven other species evolved from its sister species.
Yata (1989), analysing the Old World species of the pierid genus Eurema, did not
find special links between Sulawesi and the Philippines or the Moluccas. The five spe-
cies of the tilaha subgroup occur in Sundaland, Sulawesi and the Lesser Sunda Islands.
Of these, only E. tominia occurs on Sulawesi, and is one of the very few butterflies res-
tricted to Sulawesi and Borneo. On the basis of his phylogenetic scheme for the subg-
roup, Yata concluded that the two Lesser Sunda Islands endemics, E. timorensis and E.
lombokiana, were the first split off. Then E. tominia separated on Sulawesi from the
Sundaland population. The last split was between the population of Java and Bali (E.
tilaha) and the rest of Sundaland (E. nicevillei). Finally, E. tominia spread to Borneo to
become sympatric and hybridise with E. nicevillei (Holloway, 1973; see also Yata, 1992).
The sari subgroup of eight species is divided by Yata into two sections, the sari section
of three species, distributed from Burma to Sundaland and the Philippines, but not on
Sulawesi, and the andersoni complex of five species, to which the Sulawesi endemic E.
celebensis belongs. The phylogenetic relationships of the latter complex are unresolved,
but since the complex does not occur in the Philippines or the Moluccas, the only link
shown is between Sulawesi and Sundaland. The simulatrix subgroup consists of the
Sulawesi endemic E. irena and the widespread E. simulatrix. The latter species is found
from Burma to Sundaland and the Philippines. From this distribution it cannot be
concluded whether E. irena links Sulawesi to Sundaland or to the Philippines.
As pointed out by Vane-Wright (1991), the cladistic analysis of Idea Fabricius of Kit-
ching et al. (1987), transformed into an area cladogram (Vane-Wright’s fig. 3; cf. our fig.
11), leads to the conclusion that an originally Asian ancestor first spread from Sunda-
land to Sulawesi, where it speciated, and later again spread from Sundaland to Sulawe-
si, either directly or through the Philippines. After speciating again in Sulawesi, it
spread to the Moluccas and hence to western New Guinea. This scenario is consistent
with the geological interpretation that west Sulawesi has always been close (and until
the middle Eocene connected) to Sundaland and that opportunities for exchange with
Azania camillus
acilia acilia
group eximia
themire
cocles
cocles
group
paulinus
cassander
thyonneus theresae
Cyrestis
group thyonneus
tabula
thyodamas
heracles
nais
thyodamas nivea
group irmae
lutea
risa
excellens
peraka
Chersonesia
rahria
intermedia
nicevillei
Fig. 13. Strict consensus tree of 40 equally parsimonious trees for Cyrestis and Chersonesia (Nymphali-
dae), based on data provided by Holloway (1973) (length 158, CI=0.671, RI=0.858, RI=0.576). Species
occurring in the Sulawesi Region have been printed in bold. See text for further explanation.
the Philippines and the Moluccas only became significant in the Pliocene.
As explained by Vane-Wright (1991), the phylogenetic relationships among the
eight members of the monophyletic Parantica tityoides group (Ackery & Vane-Wright,
1984) tell a different story (fig. 12). This group, which includes a monophyletic subg-
roup of four Sulawesi endemics, occurs in Sumatra, Java, Bali and Timor, but is absent
from Borneo, the Philippines and the Moluccas. Unless it has become extinct in Bor-
neo, it must have reached Sulawesi through Java and possibly the Lesser Sunda
Islands. Its occurrence on Timor indicates that extinction must have occurred in most
of the Lesser Sunda Islands. A link between Sulawesi and the Lesser Sunda Islands is
still apparent in the monophyletic group comprising Parantica sulewattan (Lompoba-
tang in south-western Sulawesi), P. philo (Sumbawa) and P. wegneri (Flores).
Smiles (1982) was aware of only one of the two endemic Polyura species known
from Sulawesi. In his cladistic analysis, the endemic P. cognata emerged as sister to P.
dehanii, found only on Sumatra and Java. In Smiles’ scheme this pair form the sister
taxon of the athamas group, seven species collectively distributed through Sri Lanka,
India, southern China, SE Asia, the Philippines, Sulawesi, and the Greater and Lesser
Sunda Islands, to Timor (Smiles, 1982: map 2). None of the athamas group species is
found in N or C Maluku, New Guinea or Australia. On Sulawesi, the group is repre-
sented by the only non-endemic Polyura found on the island, P. alphius (= agraria).
Thus P. cognata appears to be of SE Asian origin, and may have evolved on Sulawesi
following a vicariance event with, or dispersal from Java. The endemic species that
Smiles unfortunately overlooked, Polyura inopinatus, is very distinctive. It is known
only from the unique holotype, described from northern Sulawesi in 1939, and its
place within Smiles’ scheme has not been determined. P. inopinatus was not encounte-
red during Project Wallace.
The genus Cyrestis, with only five species in the Sulawesi Region (of which three
are endemic) is remarkable for the various biogeographic links it demonstrates. Hollo-
way (1973) analysed the Cyrestis group of genera, using a distance method. We re-ana-
lysed his data matrix (p. 170), applying maximum parsimony (PAUP4b10). The strict
consensus tree of the 40 equally parsimonious trees found (our fig. 13) is slightly diffe-
rent from Holloway’s dendrogram (his fig. 10). We have used Azania (with camillus as
exemplar species) to root the tree. Conspecific subspecies have been merged and the
names for species groups have been added, following Tsukada (1985). If this cladogram
truly reflects phylogenetic relationships, then the monophyly of Cyrestis is not strongly
supported (in fact, in 70% of the 40 trees the acilia group clusters with Chersonesia), and
recognition of a nivea group as does Tsukada (1985) renders the thyodamas group para-
phyletic. However, these taxonomic problems do not affect Sulawesi relationships.
We find Sulawesi taxa in four species groups. The acilia group is mainly distribu-
ted in the Papuan Region, C. strigata (recognised as a separate species here, but consi-
dered a subspecies of C. acilia by Holloway, 1973) being the representative in the Sula-
wesi Region, while the endemic C. eximia of Kep. Sangihe also belongs to this group.
Thus, these species show an eastern connection, but since the sister of the acilia group
is uncertain, nothing can be said on direction of spread.
The cocles group demonstrates an interesting sequence of speciation events, star-
ting with an early split between the Sundaland-continental Asian taxa C. themire and
C. cocles. The next split is between C. cocles and a Philippines-Sulawesi-Molluccas-
Vogelkop complex. This is a Sundaland connection, but it cannot be decided whether
the ancestor of C. cassander and C. paulinus went from Borneo directly to Sulawesi or
via the Philippines. Finally, C. paulinus apparently extended its range further east and
reached the Vogelkop, demonstrating the Moluccan connection.
In the thyonneus group we find again a Sundaland connection in the sisters C. the-
resae (Sumatra and Borneo) and C. thyonneus (Sulawesi and C. Moluccas). The thyoda-
mas group is very widespread, occurring throughout the Oriental Region, extending
north to S Japan, and east to the Solomon Islands and New Caledonia. Since the ear-
lier speciation events are between continental Asian and Sundaland taxa, the spread
would seem to have been from west to east across Wallace’s Line. In our area we have
the telamon complex of species, with C. heracles on C and N Sulawesi and Kep. Sula, C.
telamon in C and N Moluccas, C. achates in New Guinea, and additional taxa in the Bis-
marck and Solomon Islands. According to fig. 10, the sister of this complex is C. nais,
an endemic of the Lesser Sunda Islands (Lombok to Timor). This suggests a southern
connection, but because of the absence of C. heracles from the south and southeast
arms of Sulawesi (as well as from the southern islands) the possibility cannot be ruled
out that the route was from the Lesser Sunda Islands to the Moluccas (although now
absent from S Moluccas) and from there into Sulawesi.
De Jong (1983) found an exclusive link between Sulawesi and the Philippines in
laxmi continental Asia

similis Philippines
minor Philippines
kehelatha Sulawesi Region
semperi Philippines
palawana Sundaland
Fig. 14. Species and area cladogram for the laxmi group of the genus Coladenia (Hesperiidae), after de
Jong (1996). The Sulawesi species has been printed in bold.
the sister species Matapa celsina (Sulawesi endemic) and M. intermedia (Sulawesi and
the Philippines). The sister species of the two species combined is M. sasivarna, distri-
buted from NE India to Sumatra and Borneo. Sister to the three species combined are
the sister species M. aria and M. druna, both with a wide distribution in the Oriental
Region, M. aria also occurring in the Philippines. Apparently, the ancestor of M. celsina
and M. intermedia originally came from Borneo. Since M. celsina and M. intermedia
overlap in Sulawesi, it is likely that M. intermedia colonized Sulawesi after speciation
in the Philippines. Whether the common ancestor of the two came first to Sulawesi (in
which case it indicates a link between Sulawesi and Borneo) or to the Philippines (in
which case Sulawesi was twice colonized from the north) cannot be decided on the
basis of present knowledge.
Links between Sulawesi and Borneo (or rather Sundaland) are also apparent in
the sister species Gangara tumpa (Sulawesi endemic) and G. lebadea (Oriental Region
to Java, Borneo, Palawan and Leyte) (de Jong, 1992), and Pirdana ismene (Sulawesi
endemic) and P. distanti or P. hyela (both Sundaland, with northward extension on
the continent) (de Jong & Treadaway, 1993b). A very different situation occurs in the
genus Coladenia (de Jong, 1996). The only Sulawesi representative, C. kehelatha,
belongs to the laxmi group of six species which are interrelated as in fig. 14. The
Sulawesi endemic is embedded, as it were, in Philippine endemics, strongly indica-
ting an exclusive Sulawesi-Philippines connection. From fig. 14 it also follows that at
some time a Philippine species returned to Sundaland. Interesting as this may be, it
does not involve Sulawesi and therefore falls outside the scope of this paper.
The genus Taractrocera has three species on Sulawesi: T. ardonia, T. luzonensis and T.
nigrolimbata. All three occur in Sundaland, luzonensis also in the Philippines. Although
they generally indicate a Sulawesi-Sundaland link, they have very different histories,
and may have arrived in Sulawesi at very different times and from different directions
(de Jong, 2001). The genus is of Australian origin. At some time, possibly in the Mioce-
ne, it spread to Asia, where it successively speciated into T. luzonensis, T. archias (not in
Sulawesi), T. nigrolimbata and several other Asian species (see also Morley, 2000: fig.
9.27, for dispersal paths between Asia and Australia in the Miocene based on pollen
analysis). It returned to Australia and New Guinea, leaving behind a population that
eventually split into the continental Asian T. maevis and the Sundaland species T.
ardonia. Since T. ardonia is only known from W Malaysia, Borneo and the Sulawesi
Region, it would appear that it reached Sulawesi directly from Borneo. The older T.
nigrolimbata occurs from Indo-China and Malaysia through Sumatra and Java to Sumba-
wa. It is unknown from Borneo. Therefore, a direct link between Sulawesi and the Les-
ser Sunda Islands seems obvious. This is strengthened by the fact that the species can be
subdivided in two subspecies, the one from Sulawesi otherwise being restricted to the
Lesser Sunda Islands. Finally T. luzonensis, the oldest Asian species of the genus, has a
wide distribution, from Burma through Sundaland to the Philippines and the Sulawesi
Region, but not occurring on Java or the Lesser Sunda Islands. Since it (or its ancestor)
came from Australia, it may well have reached Sulawesi directly from the south-east.
Remarkably, an additional case of an originally Australian group colonizing Asia is
found in the related genus Cephrenes (de Jong, 2001). After an early Papuan-Australian
development one species reached Asia and speciated there to produce C. acalle. This
species is widespread in the Oriental Region and also occurs in the Philippines, but not
on the Lesser Sunda Islands. Since it is high in the crown of the phylogenetic tree, it is
likely that it arrived in Asia much later than Taractrocera luzonensis. Although other spe-
cies of the genus also occur in the Papuan Region, the sister species of C. acalle, Cephrenes
trichopepla, is only known from N. Queensland, suggesting that the ancestor of C. acalle
did not move to the north-west by way of New Guinea and the Moluccas. Although its
route remains unclear, it is still an Australian element in the Oriental fauna, and thus in
the fauna of Sulawesi. The same is probably true for the Sulawesi representatives of
such eastern genera as Psychonotis (Lycaenidae), and possibly Elodina (Pieridae).
Even though the cladistic information on the butterflies of the Sulawesi Region is
poor, the absence of a single pattern suggesting a single historical event to explain the
butterfly diversity of the region, is obvious. This is in agreement with information on
the geological history of the area. Apparently, Sulawesi (or its constituent parts) has
been colonized from different directions over a period of millions of years.
Note added in press: Fric et al. (submitted) have made a very interesting cladistic
analysis of the Palaearctic/Indian region genus Araschnia (Nymphalini), which they
demonstrate to be the sister group of Symbrenthia, the latter to include the former genus
Mynes. Within their expanded concept of Symbrenthia, the five Sulawesi species occupy
a diverse set of relationships. The Sulawesi endemic S. intricata forms a basal clade, sis-
ter to all the other two dozen or more members of the genus. The ‘Asian’ species S. hip-
poclus and S. lilaea, and another Sulawesi endemic, S. platena, also occupy basal lin-
eages, forming together with intricata and two other species a basal stem group of six.
Of the two crown groups, one appears to be of New Guinea origin, as it includes only
one species occurring west of Weber’s line, the Sulawesi endemic S. hippalus. Accord-
ing to Fric et al., this terminal taxon forms part of a terminal clade of three species for-
merly included in Mynes, and appears very good evidence of a Papuan origin for this
one element of the Sulawesi fauna. The very high rank accorded S. intricata also sug-
gests a relatively ancient element among the Sulawesi butterflies, comparable to stem-
group species such as the danaines Euploea magou and Idea tambusisana (Ackery &
Vane-Wright, 1984; Vane-Wright, 1991).
Conclusions
Both faunal and cladistic analysis point to a butterfly fauna of mainly Asian (Sunda-
land) origin, with no special relationship with Borneo. Generic endemism is considered
low: seven genera are endemic to the Sulawesi Region, of which only one, the satyrine
Lohora, shows evidence of extensive radiation. This, coupled with the high level of spe-
cies endemism, suggests a long but not excessive period of evolution in isolation, proba-
bly “seeded” in geological W Sulawesi by species derived from Asia and Sundaland.
Possibly ancestors of some of these species rafted on W Sulawesi, when it separated
from Borneo in the middle Eocene, and in due course speciated in isolation. The Sula-
wesi endemics are not evenly distributed over the island. Only 25.7% are widespread,
while more than twice that number (63.6%) are restricted to the northern and central
areas. This may be due to ecological rather than historical factors: the northern and, par-
ticularly, central parts of Sulawesi may offer more chances for isolation.
Since the collision of the Asian and Australian plates bringing east and west Sula-
wesi together, continuing faunal exchange has mainly been a one-way route: into
Sulawesi. However, it also seems plausible that some taxa that evolved on Sulawesi
have extended east into the Moluccas, and a few may have penetrated further east
into New Guinea and even the Solomon Islands. More rarely a few others, such as
Eurema tominia, could have spread west into Borneo. These processes seem to be con-
tinuing to the present day. For example, Melanitis boisduvalia appears to have arrived
in northern Sulawesi from the Philippines via Talaud and Sangihe in the recent past.
Similarly, Papilio demoleus appears to be in a very active process of range extension,
from the Philippines to N Sulawesi. Sometimes (at present only demonstrable in Idea
and Taractrocera) Sulawesi has been colonized more than once by the same monophy-
letic group at different times.
The Asian connection ran through the Philippines, Borneo and the Lesser Sunda
Islands, but the faunal exchange with Sundaland has probably been mainly from the
north (Philippines) and south (Java and Lesser Sundas). The first and last links are
apparent as exclusive links either at the species level or at sister group level. Further
indication of the importance of these links is found in the distribution of non-endemic
species with restricted distribution on Sulawesi (ca 30% of the non-endemic species):
contrary to the narrow endemics on Sulawesi, they are mainly found in the north and
south, suggesting that they have not yet extended their ranges further across the
island. Exclusive links with Borneo are hard to find, but this is hardly surprising as
Borneo’s present island state is recent (ca 8000 yr). The island has been connected to
the mainland for much of the time since the Cretaceous. It has also intermittently been
connected to Java in the Tertiary, and broadly so in the Quaternary. Not surprisingly,
the faunas of Java and Borneo have much in common. In the Quaternary the lowering
of the sea level during the northern Ice Ages brought Borneo relatively close to the
Philippines (Palawan actually formed a northward extension of Borneo), giving the
opportunity for further faunal exchange. As a consequence, most of the species that
Sulawesi has in common with Borneo have a much wider distribution.
At taxonomic levels above the sister group, exclusive links between Sulawesi
and the Philippines or the Lesser Sunda Islands are not apparent (e.g. there is no
genus restricted to such a combination). This could be so because species invading
Sulawesi belong mainly to more dispersive groups. The link that appeared last
seems to be with the Moluccas. The greater part of the genera and species on Sula-
wesi are widespread around the island, but do not occur in the Moluccas. The
Moluccan link is only apparent in the distribution of a number of species, not even
at the species group level. This agrees with the young age of the Moluccas: the
islands emerged not longer ago than 5 Ma. When they rose out of the sea they were
obviously devoid of butterflies, offering some Sulawesi species the opportunity to
spread eastward and eventually to reach Irian Jaya. The genus Acrophtalmia is a
good example of this that also exhibits the Philippine link: this very distinct genus is
restricted to the Philippines (not Palawan), Sulawesi, Moluccas, and the Arfak
Mountains in Irian Jaya. Since the population in the Arfak Mountains appears con-
specific with the Moluccan population, a recent eastward spread rather than a west-
ward one is clearly suggested.
The almost complete lack of any distinctly eastern taxa on Sulawesi could be explai-
ned by the strong possibility that eastern Sulawesi was completely submerged up until
the suture event, and thus did not act as a “raft” for eastern taxa. Yet in two genera of
Hesperiidae (Taractrocera and Cephrenes) an Australian origin is recognizable. In both
cases the Moluccas are not involved and it is very likely that the dispersion occurred
before the Moluccas became subaerial. Although further phylogenetic analysis may
reveal more such cases, it cannot be accidental that Taractrocera lives on grasses and
some species can even be found on the beach, while Cephrenes lives on palms, such as
coco that can also be found on beaches. Both taxa are thus potentially good colonizers.
Annotated checklist
Lepidoptera Linnaeus, 1758

(butterflies and moths)
This major insect order contains in the order of 200,000 species (Heppner, 1991),
divided amongst four suborders (Zeugloptera, Aglossata, Heterobathmiina, Glossata).
The Lepidoptera occur in all terrestrial regions of the earth (except the Antarctic conti-
nent and extreme Arctic), and appear to have evolved at least as early as the Mesozoic.
Their biology is dominated by the ecology of the early stages (mainly feeding on or wit-
hin plant tissues), and the mate-location strategies and dispersal abilities of the adults.
Key works.–– Common (1970), Barlow (1982), Whalley (1986), Holloway et al.
(1987, 2001), Stehr (1987), Nielsen (1989), Common (1990), Nielsen & Common (1991),
Scoble (1992), Robinson et al. (1994, 2001), Kristensen (1999), Pitkin 2002 (website).
Rhopalocera Boisduval, 1840

(butterflies)
The butterflies, which include about 17,500-20,000 species (Ackery et al., 1999),
belong to the Ditrysia, a major subgroup of the Glossata. The two major subgroups,
superfamilies Hesperioidea (with the single family Hesperiidae) and Papilionoidea,
are cosmopolitan and well-represented in the Sulawesi Region. A third group, the
Hedyloidea (which include about 40 known species, all restricted to the New World),
may or may not represent the closest relatives of the butterflies or even be internal to
the group (Scoble, 1986; Weller & Pashley, 1995; de Jong et al., 1996). The oldest
known fossil considered to be a hesperioid butterfly is from the Upper Paleocene
(Kristensen & Skalski, 1999). Butterfly diversification is generally considered to have
come about through co-evolution with flowering plants, or more probably by adapti-
ve radiation onto flowering plants, coupled with geographical isolation. Mate location
in butterflies is typically initiated by visually guided male activity (in contrast to
moths, in which mate location is normally initiated by controlled release of female
pheromones).
Key general works on butterflies: Ehrlich (1958), Ehrlich & Raven (1965), Hemming
(1967), Kristensen (1976), Vane-Wright (1978), Scott (1986), Scoble (1986, 1990, 1992),
Bridges (1988c), Nielsen (1989), Vane-Wright & Ackery (1989), Shields (1989a), Scoble
& Aiello (1990), Weller & Pashley (1995), de Jong et al. (1996), Ackery et al. (1999).
Key works for South East Asian and Australasian butterflies:

SE Asia: d’Abrera (1982, 1985, 1986), Aoki et al. (1982), Morishita
(1981), Tsukada & Nishiyama (1982), Tsukada (1985, 1991),
Yata (1981a);
Hong Kong: Bascombe et al. (1999);
Taiwan: Shirôzu (1960);
Laos: Motono & Negishi (1989), Osada et al. (1999);
Thailand: Pinratana (1974-1985), Pinratana & Eliot (1996);
W Malaysia: Corbet & Pendlebury (1992);
Borneo: Cassidy (1985), Otsuka (1988, 1991), Seki et al. (1991),
Maruyama (1991);
Sumatra: de Nicéville & Martin (1896);
Java: Roepke (1935-1942);
Sulawesi: Martin (1914-1929);
Philippines: Treadaway (1995);
Papua New Guinea: Parsons (1999);
Solomon Islands: Tennent (2002);
New Caledonia: Holloway & Peters (1976);
Australia: Common & Waterhouse (1981), Braby (2000), Dunn & Dunn
(1991).
For the early stages and life histories, the works of Igarashi & Fukuda (1997, 2000)
represent a remarkable resource. Chou (1990, 1998) provides illustrations of all Chine-
se butterflies, many of which are Oriental in distribution. The series on Chinese but-
terflies produced by Satoshi Koiwaya (e.g. 1996) is another remarkable source of infor-
mation on life histories. Ackery et al. (1995; see also d’Abrera, 1980) provide a catalo-
gue of the butterflies of the Afrotropical Region, which is undoubtedly the most simi-
lar major region to Indo-Australia in terms of its butterfly fauna.
Hesperiidae Latreille, 1809

(skippers)
Range.–– Cosmopolitan, but not occurring in New Zealand; about 3500 species;
one family, divided into six subfamilies, three of which are represented in the Sulawe-
si Region.
Foodplants.–– A wide variety of angiosperms.
page 54 ➞
1 5 10
2 11
3 8 12
4 9 13
Plate 1
Plate 1. Hesperiidae (Figs 1-4, Coeliadinae; Figs 5-13, Pyrginae). 1: Burara aphrodite Fruhstorfer (male,
underside), Kep. Sula (Mangole, x.1897, W. Doherty, Rothschild Bequest). 2: Hasora mixta fenestrata
Fruhstorfer (male), Kep. Banggai (1904, ex J. Waterstradt, R. Oberthür Coll.). 3: Badamia exclamationis
Fabricius (female), Sulawesi (Ujung Pandang, 1896, W. Doherty, R. Oberthür Coll.). 4: Choaspes plateni
plateni Staudinger (male), Sulawesi (ix-x, Van der Poll, H. J. Adams Bequest). 5: Celaenorrhinus ficulnea
tola Hewitson (male), Sulawesi (ix-x, Van der Poll, H. J. Adams Bequest). 6: Celaenorrhinus asmara pala-
java Staudinger (male), Sulawesi (Ujung Pandang, ? ex Swinhoe Coll.). 7: Odina chrysomelaena Mabille
(male), Sulawesi (Ujung Pandang, 1896, W. Doherty, R. Oberthür Coll.). 8: Pseudocoladenia dan eacus
Latreille (male), Sulawesi (Mt G. Lompobatang, 1000-2000 m, 1896, W. Doherty, R. Oberthür Coll.). 9:
Coladenia kehelatha Hewitson (male), Sulawesi (Palu, Biromaroe, sea level, x.1936, J. P. A. Kalis, Roth-
schild Bequest). 10: Gerosis celebica celebica Felder & Felder (male), Sulawesi (Ujung Pandang, 1896, W.
Doherty, R. Oberthür Coll.). 11: Tagiades trebellius trebellius Hopffer (male), Sulawesi (Palu, Kintabaroe,
600 ft, xi.1936, J. P. A. Kalis, Rothschild Bequest). 12: Odontoptilum angulatum helias Felder & Felder
(male), Sulawesi (S. Sulawesi, viii-ix.1891, W. Doherty, Rothschild Bequest). 13: Caprona agama agama
Moore (male), Sulawesi (J. J. Joicey Coll.).
1 17
2 9 18
19
3 10
20
4 11 21
5 12 22
6 13 23
7 14 24
8 15 25
16
Plate 2
1 5
2 6
3 7
4 8
Plate 3
1 5
2 6
3 7
4 8
Plate 4
5
1
Plate 5
1 10
2 6 11
3
7
12
9 13
5 14
Plate 6
1 11 19
2 3 12 20
5 13
21
4
14
6 15 22
7 16 23
9 8
17 24
10 18 25
Plate 7
1 10 18 29
2 11 19 30
3 20 31
12 21
4 32
13 22
5 23 33
24
6 14 34
25
35
7 15 26
8 16 27 36
9 17 28 37
Plate 8
1 4
2 5
3 7
Plate 9
1 6
2
7 12
13
3 8 14
9 15
4
19
5 11 16
Plate 10
1 5
2 6
3 7
4 8
Plate 11
1 7
2 9
3 10
5 11
6 12
Plate 12
1 6
2 7
3 8
4 10
Plate 13
1 8
2 9
3 6 10
4 7 11
5 12
Plate 14
1 6
2 7
3 8
4 9
5 10
Plate 15
Plate 16
Plate 2. Hesperiidae (Figs 1-25, Hesperiinae). 1: Halpe beturia Hewitson (male), Sulawesi (between
Maros and Tjamba, 1896, W. Doherty, R. Oberthür Coll.). 2: Psolos fuligo fuscula Snellen (male), Sulawe-
si (Ujung Pandang, 1896, W. Doherty, R. Oberthür Coll.). 3: Ancistroides longicornis Butler (female, teste
Evans), Sulawesi (Manado, ex Hamilton Druce, J. J. Joicey Coll.). 4: Notocrypta paralysos volux Mabille
(male), Philippines (Mindanao, 1903-1904, J. Waterstradt, R. Oberthür Coll.) [NOTE: N. paralysos yaya
Fruhstorfer, the subspecies found in the Sulawesi Region and Maluku, has a much narrower forewing
band]. 5: Cupitha purreea Moore (female), Sulawesi (G. Lompobatang, 1000-2000 m, 1896, W. Doherty,
R. Oberthür Coll.). 6: Zographetus abima Hewitson (female), Sulawesi (between Maros & Tjamba, 1896,
W. Doherty, R. Oberthür Coll.). 7: Plastingia tessellata tessellata Hewitson (female, underside), Sulawesi
(? Jawangan, 1903, Rolle, R. Oberthür Coll.). 8: Lotongus calathus taprobanus Plötz (female), Sulawesi
(Tombugu, 1885, H. Kühn, Godman & Salvin Coll.). 9: Gangara thyrsis Fabricius (male, underside),
Sulawesi (R. Oberthür Coll.). 10: Erionota hiraca sakita Ribbe (female), Sulawesi (Tombugu, 1885, C.
Ribbe, Godman & Salvin Coll.). 11: Ilma irvina Plötz (female), Sulawesi (E. Sulawesi, Crowley Bequest).
12: Matapa celsina Felder & Felder (male), Sulawesi (Tombugu, 1885, H. Kühn, R. Oberthür Coll.). 13:
Acerbas azona Hewitson (male), Sulawesi (S. Sulawesi, viii-ix.1991, W. Doherty, W. H. Evans Coll.). 14:
Pirdana ismene Hewitson (male), Sulawesi (Minahassa, ex P. Mabille, R. Oberthür Coll.). 15: Taractro-
cera nigrolimbata talantus Plötz (male), Sulawesi (Samanga, xi.1895, H. Fruhstorfer, Fruhstorfer Coll.).
16: Oriens alfurus Plötz (male), Sulawesi (G. Lompobatang, 1000-2000 m, 1896, W. Doherty, ex Oberthür
Coll.). 17: Potanthus fettingi nikaja Fruhstorfer (male), Sulawesi (G. Lompobatang, 1000-2000 m, 1896,
W. Doherty, R. Oberthür). 18: Telicota ternatensis testa Evans (male), Sulawesi (between Maros and
Tjamba, 1896, W. Doherty, R. Oberthür Coll.). 19: Cephrenes augiades augiades Felder & Felder (male),
Sulawesi (Mt Mata, ix.1998, A.E., Crowley Bequest). 20: Prusiana kuehni Plötz (male), Sulawesi (Ujung
Pandang, 1896, W. Doherty, R. Oberthür Coll.). 21: Parnara kawazoei Chiba & Eliot (male), “Philip-
pines” (1916, ex Swinhoe, J. J. Joicey Coll.). 22: Borbo bevani Moore (male), Sulawesi (G. Lompobatang,
1000-2000 m, 1896, W. Doherty, R. Oberthür Coll.). 23: Pelopidas agna agna Moore (male), Sulawesi (Toli
Toli, xi-xii.1895, H. Fruhstorfer, Rothschild Bequest). 24: Polytremis lubricans lubricans Herrich-Schäffer
(male), Sulawesi (between Maros and Tjamba, 1896, W. Doherty, R. Oberthür Coll.). 25: Caltoris mehav-
agga Fruhstorfer (male), Sulawesi (Ujung Pandang, 1896, W. Doherty, R. Oberthür Coll.).
Plate 3. Papilionidae (Figs 1-8, Papilioninae, Troidini). 1: Troides (Troides) hypolitus cellularis Roth-
schild (female), Sulawesi (Gorontalo, 1896, A. W. Mucks, J. J. Joicey Coll.). 2: Pachliopta polyphontes
polyphontes Boisduval (male), Sulawesi (Toli-Toli, xi-xii.1895, H. Fruhstorfer, Fruhstorfer Coll.). 3: Atro-
phaneura dixoni Grose-Smith (male), Sulawesi (Palopo, 8.vi.1975, C. G. Treadaway). 4: the same (holo-
type female), Sulawesi (N. Sulawesi, Bhool, F. Dixon, ex Grose-Smith, J. J. Joicey Coll.). 5: Troides
(Troides) helena hephaestus Felder & Felder (male), Sulawesi (Tondano, Fruhstorfer Coll.). 6: Losaria palu
Martin (male), Sulawesi (Palu, 14.iv.1983, ex D. L. Hancock). 7: Atrophaneura kuehni kuehni Honrath
(male syntype), Sulawesi (Tombugu, 1885, H. Kühn, H. J. Adams Bequest). 8: Atrophaneura kuehni
mesolamprus Rothschild (female), Sulawesi (Toli Toli, xi-xii.1895, H. Fruhstorfer, H. Fruhstorfer Coll.).
Plate 4. Papilionidae (Figs 1-8, Papilioninae, Papilionini). 1: Papilio (Menelaides) ascalaphus ascalaphus
Boisduval (female), Sulawesi (N. Sulawesi, Djiko Malobok, Bolaang Magondouw, 10.2.1927, Braekel, J. J.
Joicey Coll.). 2: Chilasa (Chilasa) veiovis Hewitson (male), Sulawesi (Ujung Pandang, 1896, W. Doherty, C.
Oberthür Coll.). 3: Papilio (Menelaides) jordani Fruhstorfer (male), Sulawesi (N. Sulawesi, Djiko Malobok,
Bolaang Magondouw, 25.vii.1927, Braekel, J. J. Joicey Coll.). 4: the same (female), Sulawesi (N. Sulawesi,
ex Niepelt, ex Joicey, H. M. Peebles Coll.). 5: Papilio (Achillides) blumei blumei Boisduval (male), Sulawesi
(Tenggari, 1898, C. Oberthür Coll.). 6: Papilio (Menelaides) sataspes sataspes Felder & Felder (female),
Sulawesi (Tondano, Fruhstorfer Coll.). 7: Papilio (Menelaides) gigon gigon Felder & Felder (male), Sulawe-
si (Gorontalo, 1896, A. W. Mucks, P. I. Lathy Coll.). 8: Papilio (Achillides) peranthus insulicola Rothschild
(male), Sulawesi (between Maros and Tjamba, 1898, W. Doherty, C. Oberthür Coll.).
Plate 5. Papilionidae (Figs 1-7, Papilioninae, Leptocircini). 1: Graphium (Paranticopsis) deucalion deu-
calion Boisduval (male), Sulawesi (Tondano, 9.10.1899, R. E. Turner Coll.). 2: Graphium (Graphium)
meyeri Hopffer (male), Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.). 3: Graphium
(Graphium) agamemnon comodus Fruhstorfer (male), Sulawesi (Tonsea Lama, 29.iii.1920, ex Zoological
Museum Buitenzorg). 4: Graphium (Graphium) monticolus Fruhstorfer (male), Sulawesi (Bua-Kraeng,
5000’, ii.1896, H. Fruhstorfer, Fruhstorfer Coll.). 5: Graphium (Pathysa) dorcus dorcus de Haan (male),
Sulawesi (no data, ?ex Honrath, H. J. Adams Bequest). 6: Graphium (Graphium) codrus celebensis Wal-
lace (male), Sulawesi (Toli-Toli, xi-xii.1895, H. Fruhstorfer, Rothschild Bequest). 7: Lamproptera meges
akirai Tsukada & Nishiyama (male), Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.).
Plate 6. Pieridae (Figs 2, 6, 14, Coliadinae; Figs 1, 3-5, 7-13, Pierinae). 1: Pareronia tritaea bargylia Fruh-
storfer (female), Sulawesi (Ujung Pandang, 1896, W. Doherty, R. Oberthür Coll.). 2: Eurema (Terias)
tominia tominia Vollenhoven (male), Sulawesi (Toli-Toli, xi-xii.1895, H. Fruhstorfer, Rothschild
Bequest). 3: Aoa affinis Vollenhoven (female), Sulawesi (Tondano, J. J. Joicey Coll.). 4: Ixias paluensis
Martin (male), Sulawesi (Palu, 15.vii.1912, L. Martin, Rothschild Bequest). 5: Hebomoia glaucippe
celebensis Wallace (female), Sulawesi (N. Sulawesi, xi-xii.1895, H. Fruhstorfer, Fruhstorfer Coll.). 6:
Gandaca butyrosa samanga Fruhstorfer (male), Sulawesi (S. Sulawesi, viii-ix.1891, W. Doherty, Roth-
schild Bequest). 7: Belenois java java Sparrman (male), Sulawesi (Palu, 14.iii.1912, L. Martin). 8: Elodina
sota Eliot (female paratype), Sulawesi (S. Sulawesi, Malino, 3000 ft, 9.iv.1937, J. N. Eliot). 9: Leptosia
lignea Vollenhoven (male), Sulawesi (Palu, 2.vi.1912, L. Martin, Rothschild Bequest). 10: Delias benasu
Martin (female), Sulawesi (C. Sulawesi, 1500m, 14.xi.1979, pres. C. G. Treadaway). 11: Cepora timnatha
filia Fruhstorfer (male), Sulawesi (G. Lompobatang, 1000-2000 m, 1896, W. Doherty, R. Oberthür Coll.).
12: Saletara panda nigerrima Holland (female), Sulawesi (S. Sulawesi, viii-ix.1891, W. Doherty, Roth-
schild Bequest). 13: Appias (Catophaga) new species (= nero zarinda ab. aurosa Fruhstorfer (male),
Sulawesi (Ujung Pandang, 1896, W. Doherty, R. Oberthür Coll.). 14: Catopsilia pomona flava Butler
(female), Sulawesi (Minahassa, Tanggari, 1898, Van der Poll, J. J. Joicey Coll.).
Plate 7. Lycaenidae (Fig. 1, Poritiinae; Figs 2-5, Miletinae; Fig. 6, Curetinae; Figs 7-25, Theclinae). 1:
Deramas nigrescens Eliot (male holotype), Sulawesi (Tawaya, north of Palos Bay, viii-ix.1896, W.
Doherty, Rothschild Bequest). 2: Allotinus (Paragerydus) albatus albatus Felder & Felder (female),
Sulawesi (Dumoga-Bone National Park, 1000 m, iii.1985, J. D. Holloway, Project Wallace Expedition). 3:
Logania obscura Röber (male), Sulawesi (Tombugu, 1885, H. Kühn, C. Oberthür Coll.). 4: Miletus leos
maximus Holland (female), Sulawesi (S. Sulawesi, Pawnuang, i.1896, H. Fruhstorfer, Fruhstorfer Coll.).
5: Spalgis epius titius Fruhstorfer (male), Java (E. Java, Malang, ix.1928, E. Overdijkink, J. J. Joicey Coll.).
6: Curetis tagalica celebensis Felder & Felder (male), Sulawesi (G. Lompobatang, 1885, C. Ribbe, Godman-
Salvin Coll.). 7: Arhopala eridanus elfeta Hewitson (female), Kep. Sula (Mangole, 1894, Platen, Rothschild
Bequest). 8: Flos apidanus palawanus Staudinger (female), Philippines (Palawan, Rothschild Bequest). 9:
Surendra vivarna samina Fruhstorfer (female), Sulawesi (Toli-Toli, xi-xii.1895, H. Fruhstorfer, Rothschild
Bequest). 10: Amblypodia narada confusa Riley (female), Sulawesi (S. Sulawesi, viii-ix.1891, W. Doherty, J.
J. Joicey Coll.). 11: Iraota rochana johnsoniana Holland (female), Sulawesi (S. Sulawesi, viii-ix.1891, W.
Doherty, Rothschild Bequest). 12: Hypothecla honos de Nicéville (female), Sulawesi (Toli-Toli, W. H.
Evans Coll.). 13: Loxura atymnus sulawesiensis Takanami (male), Sulawesi (Ujung Pandang, A. R. Wal-
lace, Godman-Salvin Coll.). 14: Horaga selina Grose-Smith (female, underside), Sulawesi (S. Sulawesi,
viii-ix.1891, W. Doherty, Rothschild Bequest). 15: Drupadia theda thaliarchus Staudinger (female),
Sulawesi (Minahassa, ex Staudinger, Godman-Salvin Coll.). 16: Tajuria cyrillus Hewitson (male),
Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.). 17: Rachana jalindra tarpina Hewitson
(male), Andaman Islands (S. Andamans, 6.vi.1924, M. L. Ferrer). 18: Dacalana anysis Hewitson (male),
Sulawesi (Minahassa, ex Staudinger, Godman-Salvin Coll.). 19: Remelana jangala orsolina Hewitson
(male), Sulawesi (Minahassa, ex Staudinger, Godman-Salvin Coll.). 20: Hypolycaena sipylus giscon Fruh-
storfer (male), Sulawesi (Birumaru, Palu, sea-level, x.1936, J. P. A. Kalis, Rothschild Bequest). 21: Binda-
hara phocides fumata Röber (female, underside), Sulawesi (Toli-Toli, xi-xii.1895, H. Fruhstorfer, Fruhstor-
fer Coll.). 22: Rapala zylda Seitz (female holotype), Lutungan Island ([nr Toli-Toli, Sulawesi], xii.1895,
H. Fruhstorfer, Fruhstorfer Coll.). 23: Deudorix epijarbas megakles Fruhstorfer (male), Sulawesi (Ujung
Pandang, 1896, W. Doherty, C. Oberthür Coll.). 24: Artipe eryx alax Eliot (male holotype), Sulawesi
(Malino, 3500 ft, 12.iv.1937, J. N. Eliot). 25: Sinthusa verriculata Snellen (male syntype of S. verena Grose-
Smith), Sulawesi (S. Sulawesi, viii-ix.1891, W. Doherty, Rothschild Bequest).
Plate 8. Lycaenidae (Figs 1-35, Polyommatinae); Riodinidae (Figs 36-37). 1: Anthene licates licates
Hewitson (male), Sulawesi (Sg. Maros, 23.iii.1937, J. N. Eliot). 2: Una usta usta Distant (male, under-
side), Malaysia (Penang Hills, 30.x.1956, M. J. V. Miller, M. J. V. Miller Coll.). 3: Petrelaea sp. (male,
underside), Malaysia (Mt Tahan, Waterstradt, Rothschild Bequest). 4: Nacaduba berenice eliana Fruh-
storfer (male, underside), Sulawesi (Maros, ix.1923, C. J. Brooks, C. J. Brooks Bequest). 5: Nacaduba
angusta pamela Grose-Smith (male), Sulawesi (S. Sulawesi, viii-ix.1891, W. Doherty, Rothschild
Bequest). 6: Prosotas nora nora Felder (male, underside), Sulawesi (between Maros and Tjamba, 1896,
W. Doherty, C. Oberthür Coll.). 7: Ionolyce helicon helicon Felder (male, underside), Sulawesi (S.
Sulawesi, viii-ix.1891, W. Doherty, Rothschild Bequest). 8: Catopyrops ancyra subfestivus Röber (male,
underside), Sulawesi (G. Lompobatang, 3000 ft, iii.1896, H. Fruhstorfer, Fruhstorfer Coll.). 9: Discolam-
pa ilissus ilissus Felder (male), Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.). 10:
Caleta caleta caleta Hewitson (male), Sulawesi (Dumoga-Bone National Park, ca 1200 m, 25.iii.1985, A.
Cassidy, Project Wallace Expedition). 11: the same (underside), 22.iii.1985. 12: Psychonotis piepersii
Snellen (male), Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.). 13: Nothodanis schaef-
fera schaeffera Erschoff (male, underside), Sulawesi (Minahassa, ex Staudinger, Godman-Salvin Coll.).
14: Jamides aratus lunata de Nicéville (male), Sulawesi (Toli-Toli, xi-xii.1895, H. Fruhstorfer, Fruhstorfer
Coll.). 15: Catochrysops strabobinna Swinhoe (male, underside), Sulawesi (Samanga, xi.1895, H. Fruh-
storfer, Fruhstorfer Coll.). 16: Lampides boeticus Linnaeus (female), Sulawesi (G. Lompobatang, 1000-
2000 m, 1896, W. Doherty, C. Oberthür Coll.). 17: Leptotes plinius plutarchus Fruhstorfer (male, under-
side), Sulawesi (G. Lompobatang, 1000-2000 m, 1896, W. Doherty, C. Oberthür Coll.). 18: Castalius fas-
ciatus adorabilis Fruhstorfer (male), Sulawesi (Dumoga-Bone National Park, Hog’s Back Ridge,
6.ii.1985, J. D. Holloway, Project Wallace Expedition). 19: the same (female, underside). 20: Zizeeria
karsandra karsandra Moore (male, underside), Kep. Tukangbesi (Tomia, xii.1901, H. Kühn, Rothschild
Bequest). 21: Zizina otis Fabricius, subsp. (male, underside), Sulawesi (G. Lompobatang, 3000 ft,
iii.1896, H. Fruhstorfer, Fruhstorfer Coll.). 22: Famegana alsulus lulu Mathew (male, underside), Vulcan
Island (xi.1913-i.1914, A. S. Meek, Rothschild Bequest). 23: Zizula hylax hylax Fabricius (male, under-
side), Sulawesi (Manado, 1896, W. Doherty, C. Oberthür Coll.). 24: Everes lacturnus Godart, subsp.
(male, underside), Sulawesi (G. Rangkoenau, 900 ft, xi.1936, J. P. A. Kalis, Rothschild Bequest). 25:
Pithecops phoenix Röber (male, underside), Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür
Coll.). 26: Megisba malaya sikkima Moore (male, underside), Sulawesi (Ujung Pandang, 1896, W. Doher-
ty, C. Oberthür Coll.). 27: Sancterila deliciosa Pagenstecher (female paratype of S. sohmai Eliot & Kawa-
zoé), Sulawesi (G. Osing, nr Pulu Pulu, 2000-2100 m, 31.vii.1980, S. InouJ). 28: Udara camenae euphon
Fruhstorfer (male), Sulawesi (Pulu Pulu, 7.i.1981, K. Sohma). 29: Acytolepis samanga Fruhstorfer
(female), Sulawesi (G. Lompobatang, 1000-2000 m, 1896, W. Doherty, C. Oberthür Coll.). 30: Celastrina
philippina gradeniga Fruhstorfer (male, underside), Sulawesi (Tombugu, 1882, C. Ribbe, Fruhstorfer
Coll.). 31: Uranobothria tsukadai Eliot & Kawazoé (male paratype, underside), Sulawesi (nr Pulu Pulu,
Parado, 2300 m, 1-15.vi.1980). 32: Monodontides kolari Ribbe (male, underside), Sulawesi (Punchak,
Palopo, 1975). 33: Euchrysops cnejus Fabricius, subsp. (male, underside), Sulawesi (Kintabaru, Palu,
600 ft, xi.1936, J. P. A. Kalis, Rothschild Bequest). 34: Chilades boopis boopis Fruhstorfer (male, under-
side), Sulawesi (G. Rangkoenau, Palu, 900 ft, xi.1936, J. P. A. Kalis, Rothschild Bequest). 35: Freyeria
putli Kollar (male, underside), Bali (Gilimanoek, sea-level, v.1935, J. P. A. Kalis, Rothschild Bequest).
36: Zemeros flegyas celebensis Fruhstorfer (male), Sulawesi (Tombugu, 1882, C. Ribbe). 37: Abisara
kausambi sabina Stichel (female), Sulawesi (Tondano, 9-10.1899, ex Van der Poll, J. J. Joicey Coll.).
Plate 9. Nymphalidae (Figs 1-7, Morphinae). 1: Amathusia (Pseudamathusia) virgata thoanthea Fruh-
storfer (male), Sulawesi (Tombugu, 1882, C. Ribbe, Godman-Salvin Coll.). 2: Amathuxidia plateni
plateni Staudinger (male), Sulawesi (Dumoga-Bone National Park, in banana trap by Sg. Tumpah,
2.viii.1985, Project Wallace Expedition). 3: the same (female), Sulawesi (S. Sulawesi, viii-ix.1891, W.
Doherty, Rothschild Bequest). 4: Amathusia (Amathusia) phidippus celebensis Fruhstorfer (male),
Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.). 5: Discophora bambusae bambusae
Felder & Felder (female), Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.). 6: the
same (male), Sulawesi (Tanggari, Minahassa, 2.ix.1898, C. Oberthür Coll.). 7: Faunis menado menado
Hewitson (male), Sulawesi (C. Oberthür Coll.).
Plate 10. Nymphalidae (Figs 1-16, Satyrinae). 1: Bletogona mycalesis mycalesis Felder & Felder
(female), Sulawesi (S. Sulawesi, viii-ix.1891, W. Doherty, Rothschild Bequest). 2: Bletogona inexspectata
Uémura (female), Sulawesi (Kintabaru, Palu, 200m, x.1936, J. P. A. Kalis, W. K. J. Roepke Coll,
Rijksmueum Leiden). 3: Melanitis boisduvalia ernita Fruhstorfer (male), Sulawesi (Dumoga-Bone
National Park, confluence of Sg. Toraut and Sg. Tumpah, in banana trap, 23.vi.85, R. L. Smiles, Pro-
ject Wallace Expedition). 4: Elymnias cumaea cumaea Felder & Felder (male), Sulawesi (Toli-Toli, xi-
xii.1895, H Fruhstorfer). 5: Lethe europa arcuata Butler (female), Sulawesi (Tondano, 9-10.1899, C.
Oberthür Coll.). 6: Zethera incerta Hewitson (male), Sualwesi (Tanggari, Minahassa, 2.ix.1898, C.
Oberthür Coll.). 7: Bletogona inexspectata Uémura (male, underside), Sulawesi (Kintabaru, Palu, 600
ft, xi.1936, J. P. A. Kalis, W. K. J. Roepke Coll., Rijksmuseum Leiden). 8: Orsotriaena jopas jopas Hewit-
son (male, underside), Sulawesi (Manado, ex Museum of Zoology, Cambridge, G. T. Bethune-Baker
Coll.). 9: Ypthima (Ypthima) gavalisi Martin (male, underside), Sulawesi (Palu, 3000 ft, 9.xi.1912, L.
Martin). 10: Mycalesis itys remulina Fruhstorfer (female syntype), Suawesi (G. Lompobatang, 3000 ft,
iii.1896, H. Fruhstorfer, Fruhstorfer Coll.). 11: Mycalesis mynois Hewitson, subsp. (male, underside),
Sulawesi (S. Sulawesi, Malino-goa, 1100 m, vi.1938, van Groenendael, ITZ Amsterdam). 12: Acroph-
talmia windorum Miller & Miller (male), Sulawesi (Dumoga-Bone National Park, Hog’s Back Ridge,
i.1985, J. D. Holloway, Project Wallace Expedition). 13: Acrophtalmia leuce chionides de Nicéville
(female), Kep. Sula (vi-ix.1918, W. J. C. Frost, Joicey Coll.). 14: Nirvanopsis hypnus Tsukada &
Nishiyama (female paratype), Sulawesi (Traja Parado, 2300 m, viii.1979, Zoologische Staatssamm-
lung München). 15: Lohora (Pseudomycalesis) tanuki Tsukada & Nishiyama (female), Sulawesi (Para-
do, 2300 m, 24.x.1980, Koiwaya, Zoologische Staatssammlung München). 16: Lohora (Physcon) imita-
trix Martin (male holotype), Sulawesi (N.W. Sulawesi, Riou, viii.1912, L. Martin, Zoologische
Staatssammlung München).
Plate 11. Nymphalidae (Figs 1-2, Charaxinae; Figs 3-8, Heliconiinae). 1: Charaxes bernardus repetitius
Butler (male), Sulawesi (N. Sulawesi, xi-xii.1895, H. Fruhstorfer, Rothschild Bequest). 2: Polyura
cognata cognata Vollenhoven (male), Sulawesi (Manado, 1906). 3: Acraea moluccana dohertyi Holland
(female), Sulawesi (S. Sulawesi, Mongoloe, 5.ix.06, L. Martin). 4: Cethosia biblis picta Felder & Felder
(male), Sulawesi (G. Lompobatang, 1000-2000 m, 1896, W. Doherty, C. Oberthür Coll.). 5: Terinos tax-
iles poros Fruhstorfer (male), Sulawesi, Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.). 6: Vin-
dula erota banta Eliot (female), Sulawesi (Djiko Malobok, Bolaang Magondouw, 100m, 20.iii.1928, C.
van Braekel, J. J. Joicey Coll.). 7: Cupha arias celebensis Fruhstorfer (female), Sulawesi (Dongala, south
of Palos Bay, viii-ix.1896, W. Doherty, Rothschild Bequest). 8: Algia satyrina satyrina Felder & Felder
(female), Sulawesi (Toli-Toli, xi-xii.1895, H. Fruhstorfer, Rothschild Bequest).
Plate 12. Nymphalidae (Figs 1-5, Heliconiinae; Figs 6-12, Biblidinae). 1: Cirrochroa thule Felder &
Felder (male), Sulawesi (S. Sulawesi, viii-ix.1891, W. Doherty, Rothschild Bequest). 2: Vagrans sinha
nupta Staudinger (male), Sulawesi (Tondano, 9.10.1899, ex Van de Poll, Adams Bequest). 3: Phalanta
alcippe celebensis Wallace (male), Sulawesi (S. Sulawesi, viii-ix.1891, W. Doherty, Rothschild Bequest).
4: Argyreus hyperbius javanica Oberthür (male), Bali (Kintamani, 4000 ft., ii-iii.1911, E. Stresemann, Roth-
schild Bequest). 5: the same (female). 6: Pantoporia antara antara Moore (male), Sulawesi (Manado,
2.ix.1897, G. T. Bethune-Baker Coll.). 7: Lasippa neriphus tawayana Fruhstorfer (male), Sulawesi (G.
Lompobatang, 1000-2000 m, 1896, W. Doherty, C. Oberthür Coll.). 8: Neptis celebica celebica Moore
(female), Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.). 9: Neptis ida celebensis Hopf-
fer (male), Sulawesi (Manado, G. T. Bethune-Baker Coll.). 10: Ariadne celebensis celebensis Holland
(male), Sulawesi (G. Lompobatang, 1000-2000 m, 1896, W. Doherty, C. Oberthür Coll.). 11: Ariadne
merionoides merionoides Holland (male), Sulawesi (G. Lompobatang, 1000-2000 m, 1896, W. Doherty, C.
Oberthür Coll.). 12: Laringa castelnaui Felder & Felder, subsp. (male), Sulawesi (Palu, G. Rangkoenau,
900 ft, xi.1936, J. P. A. Kalis, Rothschild Bequest).
Plate 13. Nymphalidae (Figs 1-10, Biblidinae). 1: Euthalia amanda amanda Hewitson (female), Sulawe-
si (Manado, Rothschild Bequest). 2: Lexias aeetes aeetes Hewitson (male), Sulawesi (Minahassa, G. Tal-
bot Coll.). 3: Dophla evelina dermoides Rothschild (male), Sulawesi (Minahassa, ex Staudinger 1887, C.
Oberthür Coll.). 4: Parthenos sylvia saltentia Hopffer (male), Sulawesi (Tondano, 7-8.1899, C. Oberthür
Coll.). 5: Chersonesia rahria celebensis Rothschild (female), Sulawesi (S. Sulawesi, viii-ix.1891, W. Doher-
ty, Rothschild Bequest). 6: Euthalia amanda amanda Hewitson (male), Sulawesi (N. Sulawesi, ex Janson
1906, C. Oberthür Coll.). 7: Cyrestis thyonneus celebensis Staudinger (male), Sulawesi (S. Sulawesi, viii-
ix.1891, W. Doherty, Rothschild Bequest). 8: Dichorragia nesimachus pelurius Fruhstorfer (male),
Sulawesi (Manado, Tonsea Lama, 5.4.1927, Braekel, J. J. Joicey Coll.). 9: Pseudergolis avesta toalarum
Fruhstorfer (male), Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.). 10: Bassarona labo-
tas Hewitson (male), Sulawesi (N. Sulawesi, C. van Braeckel, J. J. Joicey Coll.).
Plate 14. Nymphalidae (Figs 1, 5, Biblidinae; Figs 2-4, 6-12, Nymphalinae). 1: Tacola eulimene badoura
Butler (male), Sulawesi (Minahassa, G. Talbot Coll.). 2: Doleschallia polibete celebensis Fruhstorfer
(male), Sulawesi (Tondano, 3-4.1899, G. T. Bethune-Baker Coll.). 3: Kaniska canace maniliana (male),
Borneo (Mt Kinabalu, 5-8.1903, J. Waterstradt, C. Oberthür Coll.). 4: Junonia erigone gardineri Fruhstor-
fer (female), Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.). 5: Athyma libnites libnites
Hewitson (male), Sulawesi (Tondano, 3-4.1899, C. Oberthür Coll.). 6: Symbrenthia intricata Fruhstorfer
(male syntype), Sulawesi (Toli-Toli, xi-xii.1895, H. Fruhstorfer). 7: Symbrenthia hippalus Felder & Felder
(male), Sulawesi (N. Sulawesi, Rothschild Bequest). 8: Yoma sabina nimbus Tsukada (male), Sulawesi
(Kalawara, 6.vi.1912, L. Martin). 9: Rhinopalpa polynice megalonice Felder & Felder (male, underside),
Sulawesi (S. Sulawesi, viii-ix.1891, W. Doherty, Rothschild Bequest). 10: Vanessa buana Fruhstorfer
(male), Sulawesi (G. Lompobatang, 5000-7000 ft, x.1895, A. Everett, Rothschild Bequest). 11: Sym-
brenthia hippalus Felder & Felder (female), Sulawesi (N. Sulawesi, C. Hose, Rothschild Bequest). 12:
Hypolimnas anomala stellata Fruhstorfer (male), Sulawesi (S. Sulawesi, viii-ix.1891, W. Doherty, Roth-
schild Bequest).
Plate 15. Nymphalidae (Figs 1-4, Apaturinae; Fig. 5, Libytheinae; Figs 6-10, Danainae). 1: Rohana
macar macar Wallace (female), Sulawesi (Ujung Pandang, 1896, W. Doherty, C. Oberthür Coll.). 2: Hel-
cyra hemina borneenesis Hall (holotype male), Borneo (Mt Kinabalu, 5-8.1903, J. Waterstradt, C.
Oberthür Coll.). 3: Hestinalis divona Hewitson (male), Sulawesi (C. Sulawesi, 17.ix.1975, ex C. G.
Treadaway). 4: Euripus robustus Wallace (male), Sulawesi (Manado, J. J. Joicey Coll.). 5: Libythea geof-
froy celebensis Staudinger (male), Sulawesi (Dumoga-Bone National Park, Toraut crossing at wet sand,
ii.1985, J. D. Holloway, Project Wallace Expedition). 6: Ideopsis juventa tontoliensis Fruhstorfer (male),
Sulawesi (N. Sulawesi, Tanggari, 1898, P. I. Lathy Coll.). 7: Tirumala choaspes kalawara Martin (male),
Sulawesi (Palu, 15.i.1913, L. Martin). 8: Danaus (Salatura) genutia leucoglene Felder & Felder (male),
Sulawesi (N. Sulawesi, Tanggari, C. Oberthür Coll.). 9: Danaus (Anosia) chrysippus chrysippus Linnaeus
(male), Sulawesi (N. Sulawesi, H. Fruhstorfer, Fruhstorfer Coll.). 10: Parantica sulewattan Fruhstorfer
(female), Sulawesi (G. Lompobatang, 1000-2000 m, 1896, W. Doherty, C. Oberthür Coll.).
Plate 16. Nymphalidae (Figs 1-3, Danainae). 1: Euploea magou Martin (male), Sulawesi (Palopo,
viii.1978, ex T. Fujioka). 2: Idea blanchardii blanchardii Marchal (male), Sulawesi (Manado, A. R.
Wallace, Hewitson Coll.). 3: Idea tambusisiana hideoi Okano (male), Sulawesi (Pendoro, 70 km south of
Lake Poso, 1200-1500 m, ex Y. Nishiyama).
Key works.–– Evans (1949), Corbet & Pendlebury (1992), Common & Waterhouse
(1981), Ackery (1989), Maruyama (1991), de Jong & Treadaway (1993c), Bridges (1994),
Ackery et al. (1999), Braby (2000).
Coeliadinae Evans, 1937

(= Rhopalocamptinae Evans, 1934; unnecessary replacement name:
ICZN 1999 Art. 40; Lamas et al., in prep.).
(awls and awlets, policemen — Pl. 1, figs 1-4)
Range.–– Palaeotropics; a small group of about 80 species, often crepuscular in

habit, included in about seven genera – five of which occur in Sulawesi.
Foodplants.–– Asclepiadaceae, Araliaceae, Barringtoniaceae, Bignoniaceae, Com-
bretaceae, Connaraceae, Corynocarpaceae, Euphorbiaceae, Fabaceae, Geraniaceae, Ica-
cinaceae, Malpighiaceae, Malvaceae, Menispermaceae, Moraceae, Myristicaceae, Myr-
sinaceae, Nyctaginaceae, Oleaceae, Rubiaceae, Sabiaceae, Solanaceae, ?Zingiberaceae.
Key works.–– As family.
Burara Swinhoe, [1893]

(awls and awlets — Pl. 1, fig. 1)
Range (1+2+5+6+7): Sri Lanka, India and China to Malay Peninsula, Greater and
Lesser Sunda Islands, Philippines and Sulawesi Region. Sixteen species formerly
included in Bibasis (de Jong & Treadaway, 1993c; Tsukiyama, 1985). Apart from morp-
hological characteristics, they differ from Bibasis in being crepuscular (Maruyama,
1991). Chiba (1995, 1997) divided the genus in two species groups, the smaller one
continental, the larger one, with 12 species, with a wider distribution, up to 6 of which
occur on Sulawesi.
Foodplants.–– Araliaceae, Combretaceae, Malpighiaceae, Myristicaceae, Myrsi-
naceae, ?Zingiberaceae.
Key works.–– Evans (1949), Tsukiyama (1985), Maruyama (1991), de Jong & Tre-
adaway (1993a).
B. oedipodea Swainson, 1820 (Branded Orange Awlet)

Range (1+2+6+7).–– Sri Lanka, India, Indo-China, Malay Peninsula, Sumatra, Java,
Borneo, Palawan, Philippines, Sulawesi Region.
Foodplants.–– Combretum (Combretaceae); Hiptage (Malpighiaceae).
–– *B. oedipodea excellens Hopffer, 1874
Range.–– Sulawesi (N, C, S), Kep. Sula (Mangole).
B. tuckeri Elwes & Edwards, 1897

(Tucker’s Awlet)
Note.–– Evans (1949) mentioned only two specimens, one from Burma, the other
from W Malaysia. Maruyama (1991) recorded the species also from S Thailand,
Sumatra and N Borneo. Igarashi & Fukuda (2000) give the distribution as mentioned
below.
Range (1+2+6+7).–– Sri Lanka, N India to Indo-China, Malay Peninsula, Sumatra,
Java, Borneo, Palawan, Mindanao, Sulawesi, Kep. Banggai and Kep. Sula.
Foodplants.–– Hiptage (Malpighiaceae) (Robinson et al., 2001). Igarashi & Fukuda
(2000) describe and illustrate the larva and pupa from the Cameron Highlands,
Malay Peninsula. The small tree on which the mature larva was found had already
been defoliated and the tree died before it could be identified.
*B. phul Mabille, 1876

(Mabille’s Awlet)
Range (E).–– Sulawesi (N, C, S).
Note.–– Tsukiyama (1985) includes phul in a largely unresolved group of six spe-
cies, including gomata. Old records for the Philippines should be discounted (see de
Jong & Treadaway, 1993c).
*B. imperialis Plötz, 1886

(Imperial Awlet)
Range (R).–– Sulawesi Region.
–– *B. imperialis imperialis Plötz, 1886
Range.–– Sulawesi (N, C, S).
–– *B. imperialis veteratrix Detani, 1983
Range.–– Kep. Banggai (Peleng).
*B. aphrodite Fruhstorfer, 1905

(Aphrodite’s Awlet — Pl. 1, fig. 1)
Range (R).–– Sulawesi (C, S), Kep. Banggai (Peleng), Kep. Sula (Mangole).
Note.–– The status of this taxon, often treated as a subspecies of B. harisa Moore,
is discussed by de Jong & Treadaway (1993a).
B. gomata Moore, 1865

(Pale Green Awlet)
Range (1+2+6+7).–– India, China, Indo-China, Thailand, Malay Peninsula, Suma-
tra, Java, Borneo, Palawan, Philippines, Sulawesi Region.
Note.–– Although originally included by Evans (1949) in the harisa-group, accor-
ding to Tsukiyama (1985) the relationships of gomata within Bibasis (now Burara)
remain unresolved.
Foodplants.–– Schefflera (= Heptapleurum); Trevesia (Araliaceae); Horsfieldia (Myris-
ticaceae); Embelia (Myrsinaceae). The early stages have been illustrated by Johnston &
Johnston (1980) and Igarashi & Fukuda (2000).
–– *B. gomata radiosa Plötz, 1885
Range.–– Sulawesi (N, S, C), Bangka, ?Kep. Banggai.
Bibabis Moore, 1881

(awls and awlets)
Range (1+2+5+6+7).–– Sri Lanka, India, China and Japan to Malay Peninsula,
Greater and Lesser Sunda Islands, Philippines and Sulawesi Region. Unlike Burara,
the species of this genus are diurnal. The genus comprises three species formerly
recognised by Tsukiyama (1985) as one of the species groups of Bibasis. Two of them
occur in the Sulawesi Region.
Note.–– Bridges (1994) listed six species for Bibasis, one of which, owstoni, belongs
to Burara, while two of the others (mahinta Moore, 1874, and nestor Möschler, 1878)
are generally considered subspecies of iluska.
Foodplants.–– Combretaceae, Malpighiaceae, Nyctaginaceae, Rubiaceae.
Key works.–– Evans (1949), Tsukiyama (1985), de Jong & Treadaway (1993a),
Maruyama (1991).
B. iluska Hewitson, 1867

Range (5+6).–– Assam, Indo-China, Java, Lesser Sunda Islands, Sulawesi Region.
–– *B. iluska iluska Hewitson, 1867
Range.–– Sulawesi (N, C, S), Kalao.
Foodplants.–– Hiptage (Malpighiaceae) (Igarashi & Fukuda, 2000, who also illu-
strate the early stages).
Note.–– Tsukiyama (1985) apparently refers to this taxon under the junior name
mahintha Moore, 1874, which represents the Assam/Burma race; the reason for aban-
doning the name iluska for the species is not clear, and mahintha is not adopted here.
Tsukiyama (op. cit.) places this butterfly as the sister of the next species, sena, in a
separate major division of the old, inclusive genus Bibasis. Bridges (1994) listed three
subspecies of iluska (subspecies mahintha, nestor Möschler, 1878, and iluska) as separa-
te species. According to Igarashi & Fukuda (2000) B. iluska (the species) is restricted
to the Sulawesi Region.
B. sena Moore, 1865

(Orange Tailed Awl)
Range (1+2+5+6+7).–– Sri Lanka, India, Indo-China, Malay Peninsula, Sumatra,
Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region. The spe-
cies looks superficially like a Hasora.
Foodplants.–– Combretum (Combretaceae); Hiptage (Malpighiaceae); Pisonia (Nyctagi-
naceae); Urophyllum (Rubiaceae). Igarashi & Fukuda (2000) illustrate the larva and pupa.
–– *B. sena senata Evans, 1934
Range.–– Sulawesi (N, C, S), Kep. Banggai.
Hasora Moore, 1881

(awls — Pl. 1, fig. 2)
Range (W).–– India and China to New Hebrides and Australia. A genus of over 30
species, divided by Evans (1949) into 6 species groups, four of which (with 10 species
recorded) occur in Sulawesi.
Foodplants.–– Fabaceae.
Key works.–– Evans (1949), de Jong (1982c).
*H. umbrina Mabille, 1891

Range (E).–– Sulawesi (N, S).
H. chromus Cramer, 1782

Range.–– From Pakistan to Australia and Fiji. Igarashi & Fukuda (2000) include
Sulawesi in their distribution map. Although the species is likely to occur there, we
have not seen specimens or pertinent literature references.
Foodplants.–– Ricinus (Euphorbiaceae); Derris, Pongamia, Pithecellobium (Fabaceae);
Swietenia, Trichilia (Meliaceae); Murraya, Toddalia (Rutaceae), Camellia (Theaceae). Iga-
rashi & Fukuda (2000) illustrate the larva and pupa, and some foodplants.
H. taminatus Hübner, 1818

(White-banded Awl)
Range (W).–– Sri Lanka, India to Indo-China, Malay Peninsula, Sumatra, Java, Les-
ser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region, N & C Maluku,
Irian Jaya (Waigeo).
Foodplants.–– Dalbergia, Derris, Millettia, Rourea (Fabaceae); Terminalia (Combre-
taceae). Igarashi & Fukuda (2000) illustrate foodplants and early stages.
–– *H. taminatus attenuata Staudinger, 1889
Range.–– Sulawesi (N, C, S), Kep. Banggai (Peleng), Kep. Sula (Sanana).
H. mixta Mabille, 1876

(Pl. 1, fig. 2)
Range (1+2+3+4+6+7).–– Indo-China, Thailand (Kimura, 1996), Malay Peninsula,
Sumatra, Java, Borneo (Maruyama, 1991), Palawan, Philippines, Sulawesi Region, N &
C Maluku.
Foodplants.–– Derris (Fabaceae).
–– *H. mixta fenestrata Fruhstorfer, 1911
Range.–– Sulawesi (N, C), Kep. Sangihe (Sangihe, Siao), Wowoni, Kep. Banggai
(Peleng), Kep. Sula (Mangole, Sanana).
H. badra Moore, 1858

(Common Awl)
Range (1+5+6+7).–– Sri Lanka, India, Indo-China, Malay Peninsula, Sumatra,
Java, Lesser Sunda Islands, Borneo, Philippines (Balabac, Calamian, Palawan – de
Jong & Treadaway, 1993c; not confirmed for other Philippine islands: Treadaway,
1995), Sulawesi (S).
Foodplants.–– Derris, Millettia, Pongamia (Fabaceae). Igarashi & Fukuda (2000) illu-
strate foodplants, larva and pupa.
–– H. badra badra Moore, 1858
Range.–– As for species except Sri Lanka.
*H. sakit Maruyama & Uehara, 1992

Note.–– Fujioka et al. (1997) synonymized this taxon with H. quadripunctata.
Maruyama (2000) defends its specific status and illustrates the holotype.
Range (E).–– Sulawesi (N, C).
H. quadripunctata Mabille, 1876

Range (2+3+6+7).–– Malay Peninsula, Sumatra, Java, Borneo, Philippines (but not
Palawan), Sulawesi, N Maluku (Halmahera, Bacan).

–– *H. quadripunctata celebica Staudinger, 1889
Range.–– Sulawesi (N, C, S), Kep. Banggai (Peleng).
Note.–– De Jong & Treadaway (1993c) list only N Sulawesi. Maruyama (2000) illu-
strates the lectotype.
H. vitta Butler, 1870

(Plain Banded Awl)
Range (1+2+7).–– India, China, Indo-China, Malay Peninsula, Sumatra, Borneo,
Palawan, Philippines, Sulawesi Region, Irian Jaya (Evans, 1949), but not listed for
Papua New Guinea by Parsons (1999).
Foodplants.–– Derris, Millettia, Phaseolodes, Pongamia, Spatholobus (Fabaceae).
Johnston & Johnston (1980) illustrate the pupa.
–– *H. vitta sula Evans, 1932
Range.–– Sulawesi (N, C), Kep. Banggai (Peleng), Kep. Sula (Sanana).
H. moestissima Mabille, 1876

Range (2+4).–– Philippines, Sulawesi (N, C, S), Kep. Banggai, central Maluku
(Saparua: de Jong, 1982c), ?Aru (de Jong, 1982c).
Note.–– Evans (1934) separated the single known specimen from the Aru Islands
as ssp. unica, but he did not trust the locality. Previous records for Palawan apparently
relate to H. caeruleostriata de Jong, 1982, which originally was described as a subspe-
cies of H. moestissima.
H. khoda Mabille, 1876

(Large Banded Awl)
Range (W).–– Assam, Indo-China, Malay Peninsula, Sumatra (de Jong, 1982c),
Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region, N & C
Maluku, New Guinea region, Solomon Islands, New Caledonia, Lifu, Australia.
Foodplants.–– Millettia (Fabaceae); in Australia also found on introduced Wisteria
(Fabaceae) (Braby, 2000).
–– *H. khoda burgeri Ribbe, 1889
Range.–– Sulawesi (N, C, S), Kep. Talaud, Kep. Sangihe (Siao), Kep. Banggai
(Peleng; Nieuwenhuis, 1946), Tukangbesi (Kaledupa).
H. leucospila Mabille, 189

(Violet Awl)
Range (1+2+4+6+7).–– Indo-China, Thailand, Sumatra, Java, Borneo, Palawan
(Treadaway, 1995), Philippines, Sulawesi (N, C), Maluku (Ambon).
–– H. leucospila leucospila Mabille, 1891
Range.–– As for species except Maluku.
Badamia Moore, 1881

(awls — Pl. 1, fig. 3)
Range (W).–– Sri Lanka, Pakistan, India, Indo-China, Malay Peninsula, Sumatra,
Maluku, New Guinea region, Solomon Islands, Pacific islands, Australia. A genus
containing two species, one widespread including Sulawesi and the Pacific, the other
restricted to the Pacific.
Foodplants.–– Bignoniaceae, Combretaceae, Fabaceae, Malpighiaceae, ?Moraceae,
Oleaceae.
Key works.–– Evans (1949).
B. exclamationis Fabricius, 1775

(Brown Awl — Pl. 1, fig. 3)
Range (W).–– As for genus, including Sulawesi (N, C, S), Kep. Tukangbesi
(Tomea), Salayar, Kep. Banggai (Peleng).
Foodplants.–– Bignonia (Bignoniaceae), Anogeissus, Combretum, Terminalia (Combre-
taceae); Pongamia (Fabaceae); Hiptage, Rhyssopteryx, Tristellateia (Malpighiaceae); ?Ficus
(Moraceae); Chionanthus, Linociera (Oleaceae); ?Bambusa (Poaceae). Igarashi & Fukuda
(1997) illustrate larva and pupa.
Choaspes Moore, 1881

(awlkings — Pl. 1, fig. 4)
Range (1+2+3+4+6+7).–– Sri Lanka, India, Indo-China, Malay Peninsula, Sumatra,

Java, Borneo, Palawan, Philippines, Sulawesi, N & C Maluku, New Guinea. Evans
(1949) recognised six species but, on the basis of immature stages Igarashi (1992) and
Igarashi & Fukuda (1997) convincingly demonstrated that there were more. Depen-
ding on the taxonomic rank attached to apparently monophyletic but allopatric island
forms, 7-11 species can be distinguished. Whatever scheme is applied, only two have
been found on Sulawesi.
Foodplants.–– Combretaceae, Icacinaceae, Menispermaceae, Sabiaceae, Sapindaceae.
Key works.–– Evans (1949), Chiba (1988), Igarashi (1992), Tsukiyama (1992), Chiba
(1992), de Jong & Treadaway (1993a,c), Igarashi & Fukuda (1997).
C. plateni Staudinger, 1888

(Pl. 1, fig. 4)
Range (1+2+6+7).–– Assam to Sundaland, Philippines and Sulawesi (Evans, 1949;
de Jong & Treadaway, 1993c).
Note.–– This is the conventional interpretation, in accordance with Maruyama
(1991), Corbet & Pendlebury (1992) and de Jong & Treadaway (1993a, c). The species
defined in this way is based on an apparently autapomorphic secondary sexual
character. It can be divided into a number of allopatric forms, some of which Chiba
(1992) and Tsukiyama (1992) recognise as distinct species (see also de Jong & Tre-
adaway, 1993c: 19). According to these authors C. plateni is a species restricted to
Sulawesi.
Foodplants.–– Meliosma (Meliosmaceae); Pometia (Sapindaceae) (recorded by Iga-
rashi & Fukuda, 1997, who also illustrate larva and pupa).
–– *C. plateni plateni Staudinger, 1888
C. hemixanthus Rothschild & Jordan, 1903

(Hooked Awlking)
Range (3).–– Sulawesi, Halmahera, New Guinea (Igarashi & Fukuda, 1997). Each
island has its own subspecies.
Note.–– Evans (1949), Chiba (1992) and Tsukiyama (1992) agree in the occurrence
of a subspecies of this species, furcatus Evans, 1932, in the Asian continent (Nepal to
Indo-China and S China, with unconfirmed and improbable occurrence on Palawan),
thus making the species highly disjunct. Igarashi & Fukuda (1997) consider furcatus a
distinct species on the basis of differences in the immature stages. From a bioge-
ographical point of view the opinion of the last authors seems most likely. Without
presenting new evidence, Parsons (1999) suggests that the continental furcatus as well
as the three island subspecies could be four different species. We follow Igarashi &
Fukuda (1997).
Foodplants.–– Rhyticaryum (Icacinaceae); Meliosma (Meliosmaceae); Pycnarrhena
(Menispermaceae); Sabia (Sabiaceae). Igarashi & Fukuda (1997) illustrate larva and pupa.
–– *C. hemixanthus wallacei Tsukiyama & Chiba, 1991
Range.–– Sulawesi (C).
Pyrginae Burmeister, 1878

(flats, angles, elfs, grizzled skippers — Pl. 1, figs 5-13)
Range.–– Cosmopolitan, about 1200 species in total; in Old World about 300 spe-
cies in 40 genera; eight of these genera occur in Sulawesi.
Foodplants.–– Dicotyledons (with rare exceptions).
Key works.–– Evans (1949), Corbet & Pendlebury (1992), Common & Waterhouse
(1981), Bridges (1994), Ackery et al. (1999)
Celaenorrhinus Hübner, 1819

(flats, sprites — Pl. 1, figs 5, 6)
Range (W).–– Pantropical, but not extending to New Guinea or Australia. Of the
approximately 90 species, more than 30 occur in the Oriental Region, including four
on Sulawesi (mainly in the south).
Foodplants.–– Acanthaceae, Fabaceae, Gesneriaceae, Oleaceae, Verbenaceae.
Key works.–– Evans (1949), de Jong (1982a).
C. ficulnea Hewitson, 1868

(Velvet Flat — Pl. 1, fig. 5)
Range (1+3+4+7).–– Indo-China, Malay Peninsula, Sumatra, Borneo, Palawan
(Treadaway, 1995), Sulawesi, Buru, northern Maluku.
Foodplants.–– Didissandra (Gesneriaceae) (Igarashi & Fukuda, 2000, who also illu-
strate the foodplant, larva and pupa).
–– C. ficulnea tola Hewitson, 1878
Range.–– Sulawesi (N, S), Maluku (Ternate).
C. ruficornis Mabille, 1878

(Tamil Spotted Flat)
Range (6).–– India, Java, Sulawesi Region.
Foodplants.–– Phaulopsis, Strobilanthes (Acanthaceae). Igarashi & Fukuda (2000)
illustrate foodplant, larva and pupa.
–– *C. ruficornis area Plötz, 1885 (=Celaenorrhinus chamunda subconcolor Röber, 1940;
see Evans, 1957b: 749, as “subcincolor”)
Range.–– Sulawesi (S), Kep. Banggai (Peleng).
C. asmara Butler, 1879

(White-banded Flat — Pl. 1, fig. 6)
Range (1+6+7).–– Assam, Indo-China, Thailand, Malay Peninsula, Sumatra, Java,
Borneo, Palawan, Sulawesi.
Foodplants.–– Gendarussa (Acanthaceae) (Igarashi & Fukuda, 2000); Jasminum
(Oleaceae) (Maruyama, 1991; Igarashi & Fukuda, 2000). The old record of Cleroden-
drum (Verbenaceae) (Piepers & Snellen, 1910) needs confirmation.
–– C. asmara palajava Staudinger, 1889
Range.–– Borneo, Palawan, Sulawesi (S).
C. dhanada Moore, 1865

(Himalayan Yellow-banded Flat)
Range (5+6+7).–– India, Indo-China, Sumatra, Borneo, Java, Bali, Lombok, Sulawesi.
Foodplants.–– Phaulopsis (Acanthaceae) (Igarashi & Fukuda, 2000, who illustrate
foodplant, larva and pupa).
–– *C. dhanada snelleni Fruhstorfer, 1909
Range.–– Sulawesi (S).
Odina Mabille, 1891

(flats — Pl. 1, fig. 7)
Range (1+2+7).–– Sikkim, Assam, Burma, Indo-China, Malay Peninsula, Sumatra,

Borneo, Palawan, Philippines (including Luzon and Mindanao: de Jong & Treadaway,
1993c; Tsukiyama & Chiba, 1994; Treadaway, 1995), Sulawesi Region. Evans (1949)
recognised two species, one of which was split into three allopatric species by Tsukiy-
ama & Chiba (1994). The latter authors are followed here.
Key works.–– Evans (1949), Tsukiyama & Chiba (1994).
*O. chrysomelaena Mabille, 1891

(Polygon Flat — Pl. 1, fig. 7)
Range (R).–– Sulawesi (N, C, S), Kep. Sula (Sanana).
Pseudocoladenia Shirôzu & Saigusa, 1962

(pied flats — Pl. 1, fig. 8)
Range (5+6+7).–– India, China, Indo-China, Malay Peninsula, Sumatra, Java, Les-
ser Sunda Islands, Borneo, Sulawesi (monobasic).
Note.–– Shimonoya & Murayama (1976) described a second species (pinsbukana) in

the genus, but it belongs to Coladenia (de Jong, 1996).
Foodplants.–– Amaranthaceae (Achyranthes, Cyathula). The record of Mimosa
(Mimosaceae) (Fleming, 1983) needs confirmation.
Key works.–– Shirôzu & Saigusa (1962), Corbet & Pendlebury (1992).
P. dan Fabricius, 1787

(Fulvous Pied Flat — Pl. 1, fig. 8)
Range (5+6+7).–– As genus.
Foodplants.–– As genus. Igarashi & Fukuda (2000) illustrate foodplants and
early stages.
–– P. dan eacus Latreille, 1823
Range.–– Java, Lesser Sunda Islands, Sulawesi (S).
Coladenia Moore, 1881

(pied flats — Pl. 1, fig. 9)
Range (1+2+5+6+7).–– Sri Lanka, India and China to Java, Lesser Sunda Islands,
Philippines and Sulawesi. About 15 species, only one of which occurs in the Sulawesi
Region.
Foodplants.–– Euphorbiaceae, Fabaceae, Rosaceae, Rutaceae, Sapindaceae, Tiliaceae.
Key works.–– Evans (1949), Corbet & Pendlebury (1992), de Jong & Treadaway
(1992b), de Jong (1996).
*C. kehelatha Hewitson, 1878

(Pl. 1, fig. 9)
Range (R).–– Sulawesi (N, C, S), Kep. Sula (Mangole, Sanana).
Gerosis Mabille, 1903

(white, or yellow-breasted flats — Pl. 1, fig. 10)
Range (1+2+6+7).–– Eastern Palaearctic (China), India, Indo-China, Malay Penin-

sula, Sumatra, Java, Borneo, Palawan (Treadaway, 1995), Philippines, Sulawesi Region.
Six species, of which only one, an endemic, occurs in Sulawesi.
Foodplants.–– Fabaceae (Abrus, Dalbergia).
Key works.–– Evans (1949), Corbet & Pendlebury (1992).
*G. celebica Felder & Felder, 1867

(Pl. 1, fig. 10)
–– *G. celebica celebica Felder & Felder, 1867
Range.–– Sulawesi (N, C, S), Bangka, Kep. Banggai.
–– *G. celebica sulina Evans, 1932
Range.–– Kep. Sula (Mangole, Sanana), Buton, Kep. Tukangbesi (Kaledupa, Tomea).
Tagiades Hübner, 1819

(snow or clouded flats — Pl. 1, fig. 11)
Range (W).–– Palaeotropics. About 16 species in total, of which the dozen or so

occurring in the Indo-Australian region can be divided into two species groups, both
represented on Sulawesi by single species.
Foodplants.–– Convolvulaceae, Dioscoreaceae, ?Poaceae, Roxburghiaceae, Smi-
lacaceae, ?Tiliaceae.
T. japetus Stoll, 1781

(Common Snow Flat, or Black and White Flat)
Range (W).–– Sri Lanka, India, Indo-China, Malay Peninsula, Sumatra, Java, Les-
ser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region, N & C Maluku,
New Guinea region, Solomon Islands, Australia.
Foodplants.–– Ipomoea (Convolvulaceae); Dioscorea (Dioscoreaceae); Shorea (Dipte-
rocarpaceae); Smilax (Smilaceae); ?Zea (Poaceae); Roxburghiaceae. Igarashi & Fukuda
–– *T. japetus prasnaja Fruhstorfer, 1910
Range.–– Sulawesi (N, C, S), Kep. Banggai (Peleng), Salayar.
–– *T. japetus obscurata Staudinger, 1859
Range.–– Kep. Sangihe.
–– *T. japetus navus Fruhstorfer, 1910
Range.–– Kep. Sula (Mangole, Sanana), Kep. Tukangbesi (Kaledupa).
T. trebellius Hopffer, 1874

(Pl. 1, fig. 11)
Range (1+2+3+4+5+7).–– Lesser Sunda Islands, Borneo, Palawan, Philippines,
Sulawesi Region, N & C Maluku (Maruyama, 1991), New Guinea, Solomon Islands.
Foodplants.–– Dioscorea (Dioscoreaceae). Igarashi & Fukuda (1997) illustrate larva
and pupa.
–– T. trebellius trebellius Hopffer, 1874
Range.–– Sulawesi (N, C, S), Kep. Banggai (Peleng), Lesser Sunda Islands (Leti).
–– *T. trebellius mitra Mabille, 1895
Range.–– Kep. Sula (Mangole, Sanana).
–– *T. trebellius sem Mabille, 1883
Range.–– Kep. Talaud, Kep. Sangihe.
Odontoptilum de Nicéville, 1890

(angles — Pl. 1, fig. 12)

Java, western Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi. A small
group of three species, only one of which occurs in Sulawesi; of the other two, one
occurs in Sundaland, while the other is restricted to the Philippines.
Foodplants.–– Bombacaceae, Malvaceae, Sapindaceae, Tiliaceae.
O. angulatum Felder, 1862

(chestnut angle — Pl. 1, fig. 12)
Range (2+5+6+7).–– As genus, except not recorded from Palawan (Treadaway, 1995).
Foodplants.–– Ceiba, Eriodendron (Bombacaceae); Hibiscus, Urena (Malvaceae); Allo-
phylus (Sapindaceae); Grewia, Microcos (Tiliaceae). Igarashi & Fukuda (1997) illustrate
all life stages. Bascombe et al. (1999) illustrate the pupa.
–– *O. angulatum helias Felder & Felder, 1867
Caprona Wallengren, 1857

(angles, ragged skippers — Pl. 1, fig. 13)
Range (5+6).–– Africa, Sri Lanka, India, China, Indo-China, Java, Lesser Sunda
Islands, Sulawesi. Six species; of the three Oriental Region species, the two not found
in Sulawesi are restricted to the Asian mainland and Sri Lanka. The genus has not
been recorded from the Malay Peninsula, Sumatra, Borneo or the Philippines.
Foodplants.–– Sterculiaceae, Tiliaceae, Urticaceae.
C. agama Moore, 1858

(Spotted Golden Angle — Pl. 1, fig. 13)
Range (5+6).–– India, Indo-China, Java, Lesser Sunda Islands, Sulawesi (S).
Foodplants.–– Microcos (Tiliaceae); Laportea (Urticaceae). Igarashi & Fukuda (2000)
illustrate a foodplant and the larva and pupa.
–– C. agama agama Moore, 1858
Range.–– As for species, except Lesser Sunda Islands.
Hesperiinae Latreille, 1809

(bobs, redeyes, darters, swifts and skippers — Pl. 2)
Range.–– Cosmopolitan, about 2000 species in total; about 300 in the Oriental and
Australian Regions, included in over 50 genera, of which about 24 occur in the Sula-
wesi Region.
Foodplants.–– Monocotyledons (with rare exceptions - probably only Cupitha
Moore, Udaspes Moore and Zographetus Watson amongst Asian genera: Corbet &
Pendlebury, 1992; T. Larsen, pers. comm.).
Key works.–– Evans (1949), Common & Waterhouse (1981), Corbet & Pendlebury
(1992), Bridges (1994), Ackery et al. (1999).
Halpe Moore, 1878

(aces — Pl. 2, fig. 1)
Range (1+2+6+7).–– Sri Lanka, India, China, Indo-China, Malay Peninsula, Suma-
tra, Java, Bali, Borneo, Palawan, Philippines, Sulawesi. A genus of some 35 Oriental
species; the Sulawesi Region, with three endemic species, represents its eastern limit.
Foodplants.–– Poaceae.
Key works.–– Evans (1949), Bedford Russell (1984), Maruyama (1989), Tsukiyama
& Chiba (1991), de Jong & Treadaway (1993d).
*H. beturia Hewitson, 1868

(Pl. 2, fig. 1)
Range (R).–– Sulawesi (N, S), Kep. Banggai (Peleng).
Note.–– Formerly treated as conspecific with the Philippine species H. sulphurifera
Herrich-Schäffer, 1869, beturia is now considered to be distinct (de Jong & Treadaway,
1993d).
*H. damar Bedford Russell, 1984

Range (E).–– Sulawesi.
–– *H. damar damar Bedford Russell, 1984
Range.–– Sulawesi (C - Mt Tambusisi).
–– *H. damar tsukadai Maruyama, 1989
Range.–– Sulawesi (C - 50 km northeast of Palopo).
*H. albicilia Tsukiyama & Chiba, 1991

Range (E).–– Sulawesi (C).
Psolos Staudinger, 1889

(coons — Pl. 2, fig. 2)
Range (1+2+6+7).–– India, Indo-China, Malay Peninsula, Sumatra, Java, Bali, Bor-
neo, Palawan, Philippines, Sulawesi Region (monobasic).
Foodplants.–– ?Araceae, Marantaceae.
P. fuligo Mabille, 1876

(The Coon — Pl. 2, fig. 2)
Range (1+2+6+7).–– As genus.
Foodplants.–– Donax, Stachyphrynium (Marantaceae). According to Igarashi &
Fukuda (2000), who illustrate foodplant, larva and pupa, the old record of Araceae
needs confirmation.
–– * P. fuligo fuscula Snellen, 1878
Range.–– Sulawesi (N, S), Kep. Banggai (Peleng).
Ancistroides Butler, 1874

(demons — Pl. 2, fig. 3)
Range (1+2+6+7).–– India, Indo-China, Malay Peninsula, Sumatra, Java, Borneo,

Palawan, Philippines, Sulawesi, ?N Maluku. A small group of six species.
Foodplants.–– Zingiberaceae.
*A. longicornis Butler, 1874

(Longhorn Demon — Pl. 2, fig. 3)
Range (E).–– “Timor” (?Ternate, ?Sulawesi), Sulawesi (N).
Note.–– Butler, in his original description, gives “Timor Wallace” as the type infor-
mation, and “Timor” is repeated by Evans (1949). However, the single type specimen in
the BMNH collection is clearly labelled Ternate (Wallace); it appears indistinguishable
from material from northern Sulawesi, and it seems quite likely that Butler’s type did
not even come from the Moluccas, but is a mislabelled Wallace specimen from Minahas-
sa (part of Wallace’s Malay Archipelago material does appear to be mislabelled).
Notocrypta de Nicéville, 1889

(banded demons — Pl. 2, fig. 4)
Range (W).–– Eastern Palaearctic (China), Oriental and Australian Regions, from
Sri Lanka to Australia and Fiji. About a dozen species, two of which extend to China,
and another to Australia; Sulawesi has representatives of two of the species widely
distributed in the Orient.
Foodplants.–– Costaceae, Marantaceae, Musaceae, Zingiberaceae.
N. paralysos Wood-Mason & de Nicéville, 1881

(Banded Demon — Pl. 2, fig. 4)
Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region, Maluku.
Foodplants.–– Curcuma, Zingiber (Zingiberaceae).
–– N. paralysos yaya Fruhstorfer, 1911
Range.–– Sulawesi (N, C, S), Kep. Talaud, Kep. Sangihe, Kep. Banggai (Peleng),
Kep. Sula (Mangole), Maluku (Saparua).
N. feisthamelii Boisduval, 1832

(Spotted Demon)
Range (W).–– China, India, Indo-China, Malay Peninsula, Java, Lesser Sunda
Islands, Borneo, Palawan, Philippines, Sulawesi, northern and central Maluku.
Foodplants.–– Costus (Costaceae); Maranta (Marantaceae); Musa (Musaceae); Amo-
mum, Curcuma, Elettaria, Hedychium, Zingiber (Zingiberaceae).
–– *N. feisthamelii celebensis Staudinger, 1889
Range.–– Sulawesi (N, S).
Cupitha Moore, 1884

(wax darts — Pl. 2, fig. 5)
Range (1+6+7).–– India, Indo-China, Malay Peninsula, Sumatra, Java, Borneo,

Balabac, Palawan (Treadaway, 1995), Sulawesi Region (monobasic).
Foodplants.–– Boraginaceae, Combretaceae.
C. purreea Moore, 1877

(Wax Dart — Pl. 2, fig. 5)
Range (1+6+7).–– As genus, including Sulawesi (N, C, S), Kep. Sula (Mangole)
Foodplants.–– Ehretia (Boraginaceae) ; Combretum, Terminalia (Combretaceae).
Zographetus Watson, 1893

(flitters — Pl. 2, fig. 6)
Range (1+2+5+6+7).–– Northern India, Indo-China, Malay Peninsula, Sumatra,

Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi. A heterogeneous
group of about eight Oriental species, two of which occur in Sulawesi; apparently
very rare.
Foodplants.–– Fabaceae, Gnetaceae, Poaceae, Sterculiaceae. The widely differing
foodplants may reflect the morphological heterogeneity of the genus.
Z. rama Mabille, 1877

Range (2).–– Indo-China, Malay Peninsula, Sumatra, Philippines (Mindoro, Leyte,
Samar: Treadaway, 1995), Sulawesi (N).
Foodplants.–– Gnetum (Gnetaceae) (Igarashi & Fukuda, 2000, who also illustrate
foodplant, larva and pupa).
Z. abima Hewitson, 1877

(Pl. 2, fig. 6)
Range (1).–– Palawan (Treadaway, 1995), Sulawesi (N, C, S).
Foodplants.–– Pterospermum (Sterculiaceae) (Igarashi & Fukuda, 2000, who also
illustrate foodplant, larva and pupa).
Plastingia Butler, 1870

(lancers — Plate 2, fig. 7)
Range (1+2+6+7).–– Northern India, Indo-China, Malay Peninsula, Sumatra, Java,

Bali, Borneo, Palawan, Philippines, Sulawesi Region. Eliot (in Corbet & Pendlebury,
1978), in proposing the new genera Xanthoneura, Salanoemia, Pyroneura and Pemara,
reduced Plastingia to a group of six Oriental species, three of which are endemic to the
Sulawesi Region.
Foodplants.–– Arecaceae.
*P. mangola Evans, 1949

Range (R).–– Sulawesi (S), Kep. Sula (Mangole, Sanana).
*P. tessellata Hewitson, 1866

(Straw Spotted Lancer — Pl. 2, fig. 7)
Foodplants.–– Possibly Arenga (Arecaceae), like the related P. naga de Nicéville
(Assam through Sundaland to Philippines). Igarashi & Fukuda (2000) illustrate larva
and pupa.
–– *P. tessellata tessellata Hewitson, 1866
Range.–– Sulawesi (N, C, S), Bangka, Kep. Banggai, Kep. Sula (Mangole, Sanana).
–– *P. tessellata tessa Evans, 1949
*P. flavescens Felder, 1867

Lotongus Distant, 1886

(palmers — Pl. 2, fig. 8)
Range (1+2+6+7).–– Northern India, China, Indo-China, Malay Peninsula, Suma-

tra, Java, Borneo, Palawan, Philippines, Sulawesi Region. A small group of three spe-
cies, one of which extends to Sulawesi.
Key works.–– Evans (1949), Eliot (in Corbet & Pendlebury, 1978).
L. calathus Hewitson, 1876

(White-tipped Palmer — Pl. 2, fig. 8)
Range (1+2+6+7).–– Burma, Indo-China, Malay Peninsula, Sumatra, Java, Borneo,
Palawan, Philippines (Basilan: Treadaway, 1995; Mindanao: Treadaway, in litt.), Sula-
wesi Region.
Foodplants.–– Calamus, Cocos, Daemonorops, Trachycarpus (Arecaceae); remarkably,
the larvae have been found in Malaysia in apparently mutual association with Dolicho-
derus ants (Igarashi & Fukuda, 1997, who also illustrate all life stages).
–– *L. calathus taprobanus Plötz, 1885
Gangara Moore, 1881

(redeyes — Pl. 2, fig. 9)
Range (1+2+6+7).–– Sri Lanka, India, Indo-China, Malay Peninsula, Sumatra, Java,
Bali, Borneo, Palawan, Philippines, Sulawesi. A small group of four large skippers,
one of which is distributed throughout the generic range, doubtfully including Sula-
wesi, and another is a Sulawesi endemic.
Foodplants.–– Arecaceae, Musaceae.
Key works.–– Evans (1949), de Jong (1992).
G. thyrsis Fabricius, 1775

(Giant Redeye — Pl. 2, fig. 9)
Range.–– As genus, except only uncertainly recorded from Sulawesi. The record is
based on two males in BMNH from “Celebes”, reported by Evans (1949) - but this
requires confirmation before being accepted as genuine.
Foodplants.–– Arenga, Calamus, Caryota, Cocos, Eugeissona, Korthalsia, Licuala, Livis-
tona, Metroxylon, Nypa, Phoenix, Roystonea, Trachycarpus (Arecaceae); Musa (Musaceae);

Philydrum (Philydraceae). Igarashi & Fukuda (2000) illustrate the larva and pupa; the
larva is decorated with waxy filaments
*G. tumpa de Jong, 1992

Range (E).–– Sulawesi (N).
Erionota Mabille, 1878

(redeyes, banana skippers — Pl. 2, fig. 10)
Range (1+2+3+5+6+7).–– Northern India, southern China, Indo-China, Malay

Peninsula, Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sula-
wesi Region, N Maluku; E. thrax thrax, a banana pest, has extended to Mauritius
(since 1970), Guam (since 1956), Saipan (1960s), Hawaii (since 1973), and Papua
New Guinea (since 1986: see Waterhouse & Norris, 1989). A group of seven large
skippers of mainly Oriental distribution, three of which (including one endemic) are
found on Sulawesi.
Foodplants.–– Arecaceae, Musaceae, Zingiberaceae.
Key works.–– Evans (1949), de Jong & Treadaway (1992a).
E. thrax Linnaeus, 1767

(Banana Skipper, or Palm Redeye)
Range (1+2+3+5+6+7).–– As genus, including Sulawesi (N, C, S), Kep. Sangihe,
Kep. Banggai (Peleng) and Kep. Sula; not recorded from central Maluku.
Foodplants.–– Arenga, Calamus, Cocos, Elaeis, Licuala, Metroxylon, Nypa, Rhapis
(Arecaceae); Australimusa, Eumusa, Musa (Musaceae); Chrysopogon, Saccharum (Poace-
ae); Ravenala (Strelitziaceae); Curcuma (Zingiberaceae). Igarashi & Fukuda (2000) illu-
strate the early stages.
–– E. thrax thrax Linnaeus, 1767
Range.–– As species except some parts of Philippines (see Treadaway, 1995), Kep.
Sula and Maluku.
–– E. thrax hasdrubal Fruhstorfer, 1910
Range.–– Kep. Sula (Mangole, Sanana), N Maluku, New Guinea (Parsons, 1999).
E. hiraca Moore, 1881

(Pl. 2, fig. 10)
Range (1+2+6+7).–– Sikkim, Assam, Indo-China, Malay Peninsula, Nias, Java, Bor-
neo, Palawan (Treadaway, 1995), Philippines (Luzon, Mindoro, Polillo, Ticao, Leyte,
Samar, Mindanao: Treadaway, 1995), Sulawesi Region.
Note.–– Until recently this species has been known as E. acroleuca Wood-Mason &
de Nicéville, 1881 (see de Jong & Treadaway, 1992a).
Foodplants.–– Elaeis (Arecaceae).
–– *E. hiraca sakita Ribbe, 1895
Range.–– Sulawesi (N, C, S), Bangka, Kep. Banggai (Peleng), Kep. Sula (Mangole).
*E. tribus Evans, 1941

*Ilma Swinhoe, 1905

(Pl. 2, fig. 11)
Range (E).–– Sulawesi (N, C, S) (monobasic).

*I. irvina Plötz, 1886

(Pl. 2, fig. 11)
Range (E).–– As genus.
Matapa Moore, 1881

(branded redeyes — Pl. 2, fig. 12)
Range (1+2+5+6+7).–– India, southern China, Indo-China, Malay Peninsula,

Sumatra, Java, Lesser Sunda islands, Borneo, Palawan, Philippines, Sulawesi Region.
A genus of eight or nine Oriental species, two of which occur on Sulawesi.
Key works.–– Evans (1949), de Jong (1983, 1987).
*M. celsina Felder & Felder, 1867

(Pl. 2, fig. 12)
Range (R).–– Sulawesi (N, C, S), Kep. Banggai.
M. intermedia de Jong, 1983

Range (2).–– Philippines (Samar: Treadaway, 1995), Sulawesi.
–– *M. intermedia intermedia de Jong, 1983
Range.–– Sulawesi (N).
Acerbas de Nicéville, 1895

(wights — Pl. 2, fig. 13)
Range (2+6+7).–– Burma, Malay Peninsula, Sumatra, Java, Borneo, Philippines,

Sulawesi, and Kep. Banggai (Detani, 1983). A small group of seven or eight Oriental
skippers, three of which are Sulawesi endemics (but see also Chiba, 1989).
Foodplants.–– Arecaceae (Igarashi & Fukuda, 2000).
Key works.–– Evans (1949), de Jong (1982b), Bedford Russell (1984).
*A. azona Hewitson, 1866

(Pl. 2, fig. 13)
Range (R).–– Sulawesi (S), ?Kep. Banggai (Peleng; Detani, 1983).
*A. latefascia de Jong, 1982

Note.–– This and the next species belong to the A. duris complex, known from
Pulo Laut (S. Borneo), Philippines and Sulawesi. Chiba (1989) suggested that A. latef-
ascia and A. suttoni may prove to be synonymous. This could be correct, but more
material is needed to take a final decision.
*A. suttoni Bedford Russell, 1984

Note.–– Chiba (1989) describes and illustrates the female.
Pirdana Distant, 1886

(green palmers — Pl. 2, fig. 14)
Range (1+2+6+7).–– Sikkim, Indo-China, Malay Peninsula, Sumatra, Java, Borneo,

Palawan, Philippines (Luzon, Samar, Mindanao; Treadaway, 1995) and Sulawesi. A
small Oriental group of four or five species, one of which is endemic to Sulawesi.
Foodplants.–– Liliaceae (Cordyline, Dracaena, Peliosanthes).
Key works.–– Evans (1949), de Jong & Treadaway (1993b), Chiba & Tsukiyama
(1993, 1994).
*P. ismene Felder & Felder, 1867

(Pl. 2, fig. 14).
Note.–– This taxon was raised to species rank by de Jong & Treadaway (1993b),
from P. hyela.
Taractrocera Butler, 1870

(grass darts — Pl. 2, fig. 15)
Range (1+2+5+6+7).–– Eastern Palaearctic, Oriental and Australian Regions. Six-

teen species occurring from Sri Lanka and China to the Philippines, Lesser Sunda
Islands, New Guinea, Australia and Tasmania. There do not seem to be any reliable
records for the Moluccas. The seven Australian and New Guinea species on one hand,
and the Oriental species on the other, although almost completely separated geograp-
hically, are both paraphyletic groups. The three Sulawesi species all belong to the
‘Oriental series’ (de Jong, 1991, 2001; in press).
Key works.–– Evans (1949), de Jong (1991; in press).
T. ardonia Hewitson, 1868

Range (7).–– Malay Peninsula, Sumatra, Borneo, Sulawesi Region.
–– *T. ardonia ardonia Hewitson, 1868
Range.–– Sulawesi (S), Kep. Sangihe, Salayar.
T. luzonensis Staudinger, 1889 (= ziclea Plötz, 1884, sensu auctt.)

(Veined Grass Dart)
Range (1+2+7).–– Burma, Malay Peninsula, Sumatra, Borneo, Palawan, Philippines
(Treadaway, 1995), Sulawesi Region.

Note.–– Until the publication of de Jong (1991), this taxon was usually referred to
by the name T. ziclea Plötz, 1884.
–– *T. luzonensis dongala Evans, 1932
Range.–– Sulawesi (N, C), Kep. Banggai (Peleng), Kep. Sula.
–– *T. luzonensis bessa Evans, 1949
Range.–– Salayar, Kep. Tukangbesi (Kaledupa), Tanahjampea.
T. nigrolimbata Snellen, 1876 (= aliena Plötz, 1883)

(Yellow Grass Dart — Pl. 2, fig. 15)
Range (5+6).–– Indo-China, Malay Peninsula, Sumatra, Java, Lesser Sunda Islands,
Sulawesi.
Note.–– This species was formerly known as T. aliena Plötz, 1883 (see de Jong, 1991).
–– T. nigrolimbata talantus Plötz, 1885
Range.–– Lesser Sunda Islands, Sulawesi (S).
Oriens Evans, 1932

(dartlets — Pl. 2, fig. 16)
Range (1+2+5+6+7).–– Sri Lanka, India, southern China, Indo-China, Malay Penin-
sula, Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi, Fiji
and Samoa. Seven of the eight species have essentially Oriental distributions (inclu-
ding the single Sulawesi endemic), but the eighth is a disjunct Pacific species (Fiji and
Samoa, Australia).
*O. alfurus Plötz, 1885

(Pl. 2, fig. 16)
Range (E).–– Sulawesi (N, S).
Potanthus Scudder, 1872

(darts — Pl. 2, fig. 17)
Range (W).–– Eastern Palaearctic and Oriental Regions to Maluku and Waigeo
(Maruyama, 1991), but unconfirmed for mainland New Guinea (Parsons, 1999). About
30 species, four of which occur in Sulawesi.
Note.–– This genus is much in need of revision.
Foodplants.–– Poaceae. Records of other families need confirmation.
P. omaha Edwards, 1863

(The Lesser Dart)
Range (2+5+7).–– Indo-China, Malay Peninsula, Sumatra, Lesser Sunda Islands,
Borneo, Philippines (Mindanao, Tawitawi: Treadaway, 1995), Sulawesi.
–– *P. omaha nita Evans, 1934
P. fettingi Möschler, 1878

(Pl. 2, fig. 17)
Range (3+4+5+6+7).–– Sumatra, Java, Bali, Lombok, Borneo, Philippines (Luzon:
de Jong & Treadaway, 1993c), Sulawesi Region, northern and central Maluku, Waigeo.
Note.–– This species was formerly known as P. taxilus Mabille, [1879] - see Maruy-
ama (1991).
–– *P. fettingi nikaja Fruhstorfer, 1911
Range.–– Sulawesi (N, S), Kep. Talaud, Kep. Sangihe (Siao), Kep. Banggai, Kep.
Sula (Sanana), Kep. Tukangbesi (Kaledupa, Tomea), Tanahjampea, Kalao.
P. pava Fruhstorfer, 1911

Range (2).–– India, China, Indo-China, Malay Peninsula, Philippines, Sulawesi.
–– P. pava lesbia Evans, 1934
Range.–– Philippines (Luzon, Mindoro, Polillo, Dinagat, Sibuyan, Mindanao, but
excluding Palawan: Treadaway, 1995), Sulawesi (C).
P. hetaerus Mabille, 1883

Range (2).–– Philippines (Treadaway, 1995), Sulawesi (see de Jong & Treadaway,
1993c).
–– *P. hetaerus dina Evans, 1934
Telicota Moore, 1881

(darters — Pl. 2, fig. 18)
Range (W).–– Eastern Palaearctic, Oriental and Australian Regions. At least 35

species, with highest diversity in New Guinea; three species occur in Sulawesi.
Foodplants.–– Arecaceae, Flagellariaceae, Poaceae.
Key works.–– Evans (1949), Parsons (1986, 1999).
T. colon Fabricius, 1775

(Pale Darter)
Java, Lesser Sunda Islands, Palawan, Philippines, Sulawesi Region, N & C Maluku,
New Guinea, Pacific islands, Australia. Maruyama (1991) notes the lack of any record
for Borneo.
Foodplants.–– Chrysopogon, Imperata, Microstegium, Miscanthus, Ophiurus, Oryza,
Phragmites, Pennisetum, Saccharum, Setaria, Zizania (Poaceae). Igarashi & Fukuda (2000)
illustrate larva and pupa.
–– T. colon vaja Corbet, 1942
Range.–– Sumatra, Java, Lesser Sunda Islands, Palawan, Philippines, Sulawesi (N,
C, S), Kep. Sangihe, Kep. Banggai.
–– T. colon argeus Plötz, 1883
Range.–– Tanahjampea, eastern Lesser Sunda Islands, Australia.
T. ohara Plötz, 1883

(Dark Darter)
Range (W).–– Assam, Indo-China, Malay Peninsula, Sumatra, Java, Lesser Sunda
Islands, Borneo, Palawan, Philippines, Sulawesi, N & C Maluku, New Guinea.
Foodplants.–– Oryza, Setaria (Poaceae).
–– *T. ohara rahula Fruhstorfer, 1911
T. ternatensis Swinhoe, 1907

(Pl. 2, fig. 18)
Range (3+4).–– Sulawesi Region, N & C Maluku, New Guinea region, Solomon
Islands.
–– *T. ternatensis testa Evans, 1934
–– *T. ternatensis ranga Evans, 1949
Range.–– Kep. Talaud, Kep. Sangihe (Sangihe, Siao). Evans (1949) recorded 2 males
and one female from “Salayer”; probably, the specimens are mislabelled, or else they
represent a parallel development.
–– *T. ternatensis sula Evans, 1949
Cephrenes Waterhouse & Lyell, 1914

(palm darts — Pl. 2, fig. 19)
Range (W).–– Oriental and Australian Regions, from north-eastern India to Solo-
mon Islands and Australia. Of the eight species, all but one have eastern distributions.
One of the two Cephrenes found on Sulawesi represents the western species.
Key works.–– Evans (1949), Parsons (1999), Braby (2000).
C. acalle Hopffer, 1874

(Plain Palm Dart)
Range (1+2+6+7).–– India, Indo-China, Malay Peninsula, Sumatra, Java, Borneo,
Palawan, Philippines, Sulawesi.
Note.–– Until recently this species was known as C. chrysozona Plötz, 1883, but
Maruyama (1991), checking Hopffer’s type of Hesperia acalle, found it to belong to the
same taxon as Cephrenes chrysozona lompa Evans, 1934. The genitalia of the type of the
latter were checked by de Jong (pers. obs., 2001).
Foodplants.–– Calamus, Cocos, Elaeis, Ptychosperma, Roystonea (Arecaceae). Igarashi
& Fukuda (2000) illustrate larva and pupa.
–– *C. acalle acalle Hopffer, 1874 (=lompa Evans, 1934)
C. augiades Felder & Felder, 1860

(Orange Palmdart — Pl. 2, fig. 19)
Range.–– Lesser Sunda Islands, ?Sulawesi, N & C Maluku, New Guinea region,
Solomon Islands, Australia.
Foodplants.–– Many Arecaceae: Archontophoenix, Calamus, Carpentaria, Cocos, Elais

(introduced African oil palm), Hydriastele, Laccospadix, Licuala, Livistona, Ptychosperma,
Rhopalostylus, Wodyetia (many of these only known from observations in Australia, see
Braby, 2000).
–– C. augiades augiades Felder & Felder, 1860
Range: ?Sulawesi, Ambon, Seram, Gisser. The occurrence on Sulawesi is highly
uncertain. Evans (1949) mentioned three males under ssp. augiades, but only two spe-
cimens can be found in the collection in London (Ackery, pers. comm., 2001). One
would expect the Sulawesi specimens to be most similar to ssp. buruana from Buru
and not to ssp. augiades from further east. One specimen is from ‘Mt. Mata, Celebes’.
Evans (1949) suspects this to be Mt. Mada on Buru. The other specimen, only bearing
‘Celebs’ as locality could as well be mislabelled.
Prusiana Evans, 1937

(Pl. 2, fig. 20)
Range (1+2+3+4+7).–– Borneo, Palawan, Philippines, Sulawesi Region, Maluku,

Kep. Kai. A small group of three Wallacean species, all found on Sulawesi, with one
extending west to Palawan and east to Kep. Kai, one shared only with Borneo, and
one endemic.
Key works.–– Evans (1949), Maruyama (1991).
P. kuehni Plötz, 1886

(Pl. 2, fig. 20)
Range (7).–– Borneo (Kinabalu, Kalimantan, Pulo Laut - see Maruyama, 1991),
Sulawesi Region.
–– *P. kuehni kuehni Plötz, 1886
Range.–– Sulawesi (N, C, S), Kep. Banggai
*P. hercules Mabille, 1889

Range (E).–– Sulawesi (S).
P. prusias Felder & Felder, 1861

Range (1+2+3+4).–– Palawan, Philippines, Sulawesi Region, N & C Maluku.
Note.–– Old records of prusias from Borneo should be discounted; they refer to P.
kuehni insularis (see Maruyama, 1991).
–– P. prusias matinus Fruhstorfer, 1911
Range.–– Palawan, Philippines, Kep. Sangihe, ?Sulawesi (see de Jong & Treadaway,
1993c).
–– P. prusias prusias Felder & Felder, 1861
Range.–– Sulawesi (S), Kep. Banggai, Kep. Sula (Mangole, Sanana), Salayar, N & C
Maluku, Teoor.
Parnara Moore, 1881

(swifts, watchmen — Pl. 2, fig. 21)
Range (1+2+3+5+6+7).–– Palaeotropics. A small group of nine species collectively

having a very wide range, from Africa to Australia; two occur on Sulawesi.
Foodplants.–– Arecaceae, Poaceae.
Key works.–– Evans (1949), Chiba & Eliot (1991).
P. kawazoei Chiba & Eliot, 1991

(Pl. 2, fig. 21)
Range (2+7).–– Borneo, Philippines (Luzon, Visayan islands, Mindanao), Sulawesi.
Note.–– Evans (1949) recorded this species from Sulawesi under the name P. gutta-
ta andra Evans, which proved to be a misidentification (Chiba & Eliot, 1991).
P. bada Moore, 1878

(Ceylon Swift, Water Watchman)
Range (1+2+3+5+6+7).–– Sri Lanka to southern Japan, east to Lesser Sunda Islands,
Philippines, N Maluku, New Guinea (Parsons, 1999) and Australia.
Foodplants.–– Colocasia (Arecaceae); Apluda, Bambusa, Leersia, Miscanthus, Oryza,
Saccharum, Zea (Poaceae).
–– P. bada bada Moore, 1878
Range.–– Sri Lanka, India, China, Indo-China, Malay Peninsula, Sumatra, Java, Les-
ser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi (N, S), N Maluku (Bacan).
Note.–– According to Treadaway (1995) the Philippine populations are attributa-
ble to P. bada borneana Chiba & Eliot, 1991, but according to the authors of this name
ssp. borneana is restricted to Borneo.
Borbo Evans, 1949

(swifts — Pl. 2, fig. 22)
Range (W).–– Palaeotropics, with about 18 species in the Afrotropical Region (one
extending into Mediterranean region) and 5 in the Indo-Australian, two of which
occur in Sulawesi.
B. cinnara Wallace, 1866

(Rice Swift)
Range (W).–– Sri Lanka (Harish Gaonkar, pers. comm.), India, Indo-China, Malay
wesi (N, S), Kep. Sangihe, Kep. Banggai (Peleng), Kep. Sula, Maluku (no details), New
Guinea region, Solomon Islands, Vanuatu, New Caledonia, Australia.
Foodplants.–– Andropogon, Apluda, Axonopus, Brachiaria, Cymbopogon, Digitaria, Eula-
lia, Eleusine, Eragrostis, Imperata, Isachne, Ischaemum, Miscanthus, Oryza, Oplismenus, Pani-
cum, Paspalum, Pennisetum, Rottboellia, Saccharum, Setaria, Spodipogon, Urochloa, Zizania
(Poaceae).
B. bevani Moore, 1878

(Bevan’s Swift — Pl. 2, fig. 22)
Range (4+6).–– India, Burma, China, Indo-China, peninsular Thailand, Sumatra,
Java, Sulawesi (S), central Maluku, Australia. Not known from Malay Peninsula (Cor-
bet & Pendlebury, 1992).
Foodplants.–– Imperata, Oryza, Paspalum, Saccharum (Poaceae).
Note.–– Lee (1966) erected the monotypic genus Pseudoborbo for this species on the
basis of differences in the male and female genitalia with other Borbo species. We do
not accept this separation; a comparative study involving related genera is required to
justify such an action.
Pelopidas Walker, 1870

(swifts, millet skippers — Pl. 2, fig. 23)
Range (W).–– Palaeotropics, eastern Mediterranean and eastern Palaearctic. The

genus is distributed from Africa and Turkey to the south-west Pacific; two of the ten
species occur on Sulawesi.
P. agna Moore, 1866

(Common, or Bengal Swift — Pl. 2, fig. 23)
Range (W).–– Sri Lanka and Kashmir to N & C Maluku, Solomon Islands, Austra-
lia and Vanuatu.
Foodplants.–– Imperata, Ischaemum, Microstegium, Oryza, Paspalum, Saccharum,
Sorghum (Poaceae).
–– P. agna agna Moore, 1866
Range.–– Sri Lanka, India, Indo-China, Malay Peninsula, Sumatra, Java, Lesser
Sunda Islands, Borneo, Palawan, Philippines, Sulawesi (N, S), Kep. Talaud, Kep. San-
gihe, Kep. Banggai (Peleng), Kep. Sula, Kep. Tukangbesi (Kaledupa).
P. mathias Fabricius, 1798

(Small Branded or Black Branded Swift, Lesser Millet Skipper)
Range (1+2+5+6+7).–– As genus, but not recorded from northern or central Malu-
ku, and apparently absent from Australia.
Foodplants.–– Andropogon, Cymbopogon, Digitaria, Dinochloa, Imperata, Miscanthus,
Oryza, Paspalum, Saccharum, Sorghum, Zea (Poaceae). Also recorded from Caryota, Livis-
tona (Arecaceae) and Crotolaria (Fabaceae), but these records need conformation.
–– P. mathias mathias Fabricius, 1798
Range.–– Africa, Sri Lanka, India, Indo-China, Malay Peninsula, Sumatra, Java,
Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi (N, C), Kep. Banggai
(Peleng), Tanahjampea, Kalao.
Polytremis Mabille, 1904

Range (5+6+7).–– India, China, Japan, Indo-China, Malay Peninsula, Sumatra,

Java, Lesser Sunda Islands, Borneo, Sulawesi Region. About a dozen species, mostly
Indo-Chinese in distribution, but with one ranging from India through the Malay
Peninsula to the Lesser Sunda Islands and Sulawesi Region.
P. lubricans Herrich-Schäffer, 1869

(Contiguous Swift — Pl. 2, fig. 24)
Range (5+6+7).–– From India to Sulawesi, as indicated under the genus.
Foodplants.–– Imperata, Microstegium, Miscanthus (Poaceae). Igarashi & Fukuda
–– P. lubricans lubricans Herrich-Schäffer, 1869
Range.–– India, Indo-China, Malay Peninsula, Sumatra, Java, Borneo, Philippines
(Sulu archipelago: see de Jong & Treadaway, 1993c, Treadaway, 1995), Sulawesi (N, C,
S), Kep. Sangihe, Kep. Banggai (Peleng), Kep. Sula.
Caltoris Swinhoe, 1893

Range (W).–– Eastern Palaearctic, Oriental and Australian Regions, from India and
China to Solomon Islands. A genus of about 18 species, four of which occur in the
Sulawesi Region.
Foodplants.–– Poaceae (Bambusa, Imperata).
C. bromus Leech, 1894

Range (1+2+5+6+7).–– India, China, Taiwan, Okinawa, Indo-China, Malay Penin-
sula, Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines (Visayan
islands, Mindanao: Treadaway, 1995), Sulawesi (S).
Foodplants.–– Bambusa (Poaceae).
–– C. bromus bromus Leech, 1894
Range.–– As species, excluding Taiwan and Okinawa.
C. philippina Herrich-Schäffer, 1869

(Philippine Swift)
Range (1+2+3+4).–– Sri Lanka, India, Malay Peninsula, Nias, Palawan, Philippi-
nes, Sulawesi Region, N & C Maluku, New Guinea region, Solomon Islands.
–– C. philippina philippina Herrich-Schäffer, 1869
Range.–– Sri Lanka, India, Malay Peninsula, Nias, Palawan, Philippines, Sulawesi
(N, S), Kep. Talaud, Kep. Sangihe, Kep. Sula (Mangole, Sanana).
C. mehavagga Fruhstorfer, 1911

(Pl. 2, fig. 25)
Range (4).–– Sulawesi (C, S), Kep. Sula (Mangole), Maluku (Buru).
*C. beraka Plötz, 1885

Range (R).–– Sulawesi (C, S), Kep. Sangihe, Kep. Sula (Sanana).
Papilionidae Latreille, [1802]

(swallowtails and parnassians)
Range.–– Cosmopolitan; about 550 species in three subfamilies, only one of which
occurs in the Malay Archipelago, including the Sulawesi Region.
Foodplants.–– Approximately 45 families of flowering plants, amongst which the
following are particularly important: Annonaceae, Aristolochiaceae, Lauraceae, Mag-
noliaceae and Rutaceae.
Status.–– The Papilionidae are the only family of insects to have been made the
subject of an IUCN Red Data Book; the conservation status is given for each species,
following Collins & Morris (1985) and Baillie & Groombridge (1996). See also New &
Collins (1991).
Key works.–– Munroe (1961), Igarashi (1979, 1984), Haugum et al. (1980), d’Abrera
(1982), Tsukada & Nishiyama (1982), Hancock (1983b), Collins & Morris (1985),
Bridges (1988a), Corbet & Pendlebury (1992), Häuser (1993), Tyler et al. (1994), Scriber
et al. (1994), Parsons (1996a,b), Igarashi & Fukuda (1997, 2000), Häuser et al. (2001).
Papilioninae Latreille, [1802]

(birdwings, kites and swallowtails — Pls 3-5)
Range.–– Cosmopolitan; about 480 species in four tribes, three of which occur in
the Sulawesi Region.
Foodplants.–– As family.
Key works.–– Tsukada & Nishiyama (1982), Hancock (1983b), Collins & Morris
(1985), Miller (1987), Bridges (1988a).
Troidini Talbot, 1939

(birdwings, batwings, roses, windmills and clubtails — Pl. 3)
Range.–– Pantropical (except for African mainland), with weak extension into
temperate regions; about 130 species in 12 genera, 4 of which occur in the Sulawesi
Region: Troides, Atrophaneura, Losaria and Pachliopta. Ornithoptera is very doubtfully
recorded from Kep. Sula.
Foodplants.–– Aristolochiaceae.
Key works.–– Munroe (1961), Tsukada & Nishiyama (1982), Collins & Morris
(1985), Miller (1987), Parsons (1996a,b), de Jong (2003), Vane-Wright (in press a).
Troides Hübner, 1819

(birdwings — Pl. 3, figs 1, 5)
Range (W).–– Oriental Region, including Philippines, Lesser Sunda Islands, Sula-
wesi and Maluku, with one species extending into the Papuan Region. About 20 spe-
cies, in 2 subgenera (one monobasic). All species are protected under CITES.
Foodplants.–– Aristolochia, Thottea (Aristolochiaceae).
Key works.–– d’Abrera (1975), Igarashi (1979), Tsukada & Nishiyama (1982), Hau-
gum & Low (1985), Collins & Morris (1985), Miller (1987), Parsons (1996a,b), Igarashi
& Fukuda (1997), Matsuka (2001).
Troides (Ripponia) Haugum & Low, 1975

(birdwings — Pl. 3, fig. 1)
Range.–– A single species restricted to the Sulawesi Region and Maluku. Someti-
mes placed as a separate genus, but its distinction from Troides is doubtful (Matsuka,
2001: 163).
Foodplants.–– Aristolochia (Aristolochiaceae).
Key works.–– d’Abrera (1975), Tsukada & Nishiyama (1982), Haugum & Low
(1985), Collins & Morris (1985), Miller (1987), Parsons (1996a,b), Igarashi & Fukuda
(1997), Matsuka (2001).
T. (R.) hypolitus Cramer, 1775

(Rippon’s Birdwing — Pl. 3, fig.1)
Range (3+4).–– Sulawesi Region, N & C Maluku.
Foodplants.–– Aristolochia (Aristolochiaceae). Igarashi & Fukuda (1997) illustrate
all life stages (see also Igarashi, 1979; Matsuka, 2001).
Status.–– Not rare and apparently not threatened, but protected in Indonesia.
–– *T. (R.) hypolitus cellularis Rothschild, 1895
Range.–– Sulawesi, Kep. Sangihe, ?Kep. Talaud, Kep. Togian, Buton, Muna, Kep.
Tukangbesi (Wangiwangi, Tomea, Binongko), Salayar (Matsuka, 2001).
–– *T. (R.) hypolitus caelicola Haugum & Low, 1982
Range.–– Kep. Banggai (Peleng, Potil-besar).
–– *T. (R.) hypolitus sulaensis Staudinger, 1895
Range.–– Kep. Sula (Mangole, Sanana, Taliabu).
Troides (Troides) Hübner, 1819

(birdwings — Pl. 3, fig. 5)
Range.–– As genus.
Foodplants.–– As genus.
Key works.–– As genus.
T. (T.) helena Linnaeus, 1758

(Common Yellow Birdwing — Pl. 3, fig. 5)
Range (5+6+7).–– India, Indo-China, Hainan, Malay Peninsula, Sumatra, Java,
western Lesser Sunda Islands, Borneo, Sulawesi Region. This and the next four spe-
cies belong to the helena-group, comprising about 15 species with a total distribution
extending from Sri Lanka to New Guinea (including the Philippines and the Lesser
Sunda Islands).
Foodplants.–– Aristolochia, Thottea (Aristolochiaceae). Igarashi & Fukuda (1997)
illustrate the early stages (see also Igarashi, 1979; Matsuka, 2001).
Status.–– Often common, but vulnerable in places (Peninsular Malaysia); protected
in Indonesia.
–– *T. (T.) helena hephaestus Felder & Felder, 1864
Range.–– Sulawesi, Salayar, Kep. Tukangbesi (Tomea, Binongko), Kabaena, Muna,
Kabaena, Buton, Kep. Banggai (Peleng), ?Kep. Sula (Matsuka, 2001).
T. (T.) oblongomaculatus Goeze, 1779

(Eastern Yellow Birdwing)
Range (4).–– Sulawesi, central Maluku, New Guinea.
the early stages (see also Matsuka, 2001).
Status.–– Common, not threatened.
–– *T. (T.) oblongomaculatus thestius Staudinger, 1895
Range.–– Salayar, Buton, Kep. Tukangbesi, Tanahjampea (Matsuka, 2001).
–– *T. (T.) oblongomaculatus subsp. (‘Celebean form’: Haugum & Low, 1985)
Note.–– Hancock (1983b) considered the rare Sulawesi oblongomaculatus might be
examples of T. helena affected by introgression from T. haliphron; Haugum & Low
(1985) considered them to represent a relict race of uncertain status. Not included by
Matsuka (2001). Andrew Rawlins (pers. comm.) is also of the opinion that this species
does not occur on mainland Sulawesi.
–– T. (T.) oblongomaculatus bouruensis Wallace, 1865 (= mangolensis Tsukada & Nishiy-
ama, 1982)
Range.–– Kep. Sula (Mangole), Buru, Ambelau. Andrew Rawlins (pers. comm.) is of
the opinion, based on information from H. Detani, that mangolensis was based on misla-
belled material from Buru, and that T. oblongomaculatus does not occur on Kep. Sula.
T. (T.) haliphron Boisduval, 1836

(Southern Yellow Birdwing)
Range (5).–– Southern Sulawesi Region, S Maluku (Lucipara island), Lesser Sunda
Islands.
Foodplants.–– “Small-leaved Aristolochia” (Aristolochiaceae) (Matsuka, 2001, who
also illustrates all stages; see also Igarashi, 1979).
Status.–– Not known to be threatened, but protected in Indonesia.
–– *T. (T.) haliphron haliphron Boisduval, 1836
Range.–– Sulawesi (C, S, SE).
–– *T. (T.) haliphron pallens Oberthür, 1879
Range.–– Salayar.
–– *T. (T.) haliphron pistor Rothschild, 1896
Range.–– Tanahjampea, Kayuadi, Kalao, Kalaotoa, Karompa, Madu, Bonerate
(Matsuka, 2001).
–– *T. (T.) haliphron purahu Kobayashi, 1987
Range.–– Batuata.
T. (T.) criton Felder, 1860

(Halmahera Yellow Birdwing)
Range.–– ?Sulawesi, northern Maluku (including Obi).
Foodplants.–– Aristolochia (Aristolochiaceae). Matsuka (2001) illustrates the early
stages (from N. Maluku).
Status.–– Not known to be threatened, but protected in Indonesia.
–– *T. (T.) criton celebensis Wallace, 1865 [hybrid?]
Range.–– Sulawesi.
–– *T. (T.) criton selayarensis Kobayashi & Koiwaya, 1981 [hybrid?]

Note.–– According to Hancock (1983b) and Haugum (quoted in Collins & Mor-
ris, 1985), celebensis and selayarensis represent hybrids, T. helena x T. haliphron, and
thus true T. criton is not represented in the Sulawesi Region. According to Matsuka
(2001: 165), H. Detani confirmed hybrid status in 1994 by handpairing. However, it
appears that relatively numerous specimens of ‘celebensis’ have been collected in
recent years (B. d’Abrera, pers. comm.), and it is not clear if these are the result of
deliberate breeding or not. The status of these butterflies requires further investiga-
tion.
*T. (T.) dohertyi Rippon, 1893

(Sangihe Yellow Birdwing)
Range (L).–– Kep. Talaud (Salebabu, Karakelong, Kaburuang), Kep. Sangihe (San-
gihe) (Matsuka, 2001).
Foodplants.–– Aristolochia (Aristolochiaceae). Matsuka (2001) illustrates all stages.
Status.–– Listed as vulnerable by Collins & Morris (1985) and Baillie & Groom-
bridge (1996) on account of its very restricted range, and as Indeterminate by New &
Collins (1991). Protected under Indonesian legislation (as subspecies of rhadamantus, a
species otherwise restricted to the Philippines). Separation from rhadamantus is based
on adult colour difference, and may not be justified (Matsuka, 2001).
Ornithoptera Boisduval, 1832

(birdwings — not illustrated)
Range.–– ?Kep. Sula, Maluku, New Guinea, Bismarcks, Solomon Islands, Austra-
lia. All 12 species are protected under CITES.
Foodplants.–– Aristolochia, but mainly Pararistolochia (Aristolochiaceae).
Key works.–– d’Abrera (1975), Igarashi (1979), Haugum & Low (1980), Collins &
Morris (1985), Parsons (1996a,b), Matsuka (2001).
O. croesus Wallace, 1859

(Wallace’s Golden Birdwing)
Range.–– ?Kep. Sula, northern Maluku. A member of the priamus species-group
which, including croesus, is only confirmed to occur east of Weber’s Line.
Foodplants.–– Pararistolochia (Aristolochiaceae). Matsuka (2001) illustrates the
early stages (from N. Maluku; see also Igarashi, 1979).
Status.–– Vulnerable (Collins & Morris, 1985).
–– *O. croesus sananaensis Tsukada & Nishiyama, 1980
Range.–– ?Kep. Sula (Sanana).
Note.–– Almost certainly recorded in error (see Haugum & Low, 1981; Matsuka,
2001: 349), this taxon is probably based on an aberrant specimen from N Maluku (H.
Detani, pers. comm. to A. Rawlins; Peggie et al., in prep.).
There exists much disagreement about the taxonomy of the next three genera (see
Parsons, 1999: 218). Here we follow the arrangement proposed by Häuser et al. (2001).
Atrophaneura Reakirt, 1865

(batwings — Pl. 3, figs 3, 4, 7, 8)
Range (1+2+6+7).–– Nepal to Assam and Indo-China, Sundaland, Taiwan, Philip-

pines and Sulawesi; 12 species.
Note.–– Hancock (1988) treats this genus as the nox species group of Atrophaneura
(Atrophaneura).
Foodplants.–– Aristolochia, Pararistolochia, Thottea (Aristolochiaceae), Piperaceae.
Key works.–– Tsukada & Nishiyama (1982), Hancock (1983b, 1988), Collins &
Morris (1985), Miller (1987), Parsons (1996a,b).
*A. kuehni Honrath, 1886

(Kuehn’s Batwing — Pl. 3, figs 7, 8)
Foodplants.–– Thottea (Aristolochiaceae). Igarashi & Fukuda (1997) illustrate larva
and pupa.
Status.–– ?Rare (Collins & Morris, 1985); insufficiently known (New & Collins, 1991).
–– *A. kuehni mesolamprus Rothschild, 1908
–– *A. kuehni kuehni Honrath, 1886
Range.–– Sulawesi (C, E).
*A. dixoni Grose Smith, 1901

(Dixon’s Batwing — Pl. 3, figs 3, 4)
Status.–– ?Rare (Collins & Morris, 1985); insufficiently known (New & Collins, 1991).
Losaria Moore, [1902]

(clubtails — Pl. 3, fig. 6)
Range (1+6+7).–– Assam and Hainan, south to the Andamans and Nicobars, Gre-
ater Sunda Islands, Palawan and Sulawesi. Subgenus Losaria includes just four spe-
cies, none of which is found in the Philippines or to the east of Sulawesi. A single
endemic occurs on Sulawesi (Hancock, 1984), included by Miller (1987) in Pachliopta
(Losaria). Hancock (1988), however, placed Losaria as a synonym of Atrophaneura sub-
genus Pachliopta.
Foodplants.–– Aristolochia, Thottea (Aristolochiaceae), Piperaceae.
Morris (1985), Miller (1987), Parsons (1996a,b).
*L. palu Martin, 1912

(Sulawesi Clubtail — Pl. 3, fig. 6)
Range (E).–– Sulawesi (C - Palu district).
Status.–– Insufficiently known (Collins & Morris, 1985; Baillie & Groombridge,
1996). See New & Collins (1991).
Pachliopta Reakirt, [1865]

(roses — Pl. 3, fig. 2)
Range (W).–– Mainly Oriental, but extending as far as N Queensland; 16 species.

Note.–– Hancock (1988) treats Pachliopta as a subgenus of Atrophaneura.
Foodplants.–– Aristolochia, Thottea (Aristolochiaceae).
Morris (1985), Miller (1987), Page & Treadaway (1995), Parsons (1996a,b).
P. polyphontes Boisduval, 1836

(Sulawesi Rose — Pl. 3, fig. 2)
Range (3).–– Sulawesi Region, northern and ?central Maluku (?Seram: J. Weint-
raub, pers. comm.).
Note.–– No record for central Maluku is confirmed by Page & Treadaway (1995),
who interestingly suggest that P. polyphontes is most closely related to the Philippine
species, P. kotzebuea Eschscholtz.
all life stages.
Status.–– Not known to be threatened.
–– *P. polyphontes polyphontes Boisduval, 1836
Range.–– Sulawesi, Kep. Sangihe, Kep. Talaud, Wowoni, Muna, Kabaena (Jurri-
aanse & Lindemans, 1920)
–– *P. polyphontes aipytos Fruhstorfer, 1908
Range.–– Kep. Banggai (Peleng), Kep. Sula (Taliabu, Mangole, Sanana), ?Kasiruta
(Fujioka et al., 1997).
–– *P. polyphontes rosea Oberthür, 1879
P. adamas Zinken 1831

(Zinken’s Rose)
Range (P).–– Enganno, Java, Kangean, Bawean, Tanahjampea, western Lesser
Sunda Islands, from Bali to Flores (see Page and Treadaway, 1995, who have only
recently separated this taxon from P. aristolochiae Fabricius).
Foodplants.–– Probably Aristolochia, Thottea (Aristolochiaceae).
Status.–– Not threatened.
–– *P. adamas agricola Tsukada & Nishiyama, 1980
Range.–– Tanahjampea.
Papilionini Latreille, [1802]

(mimes, helens, mormons, peacocks and swallowtails — Pl. 4)
Range.–– Cosmopolitan; about 210 species in three genera, two of which occur in
Sulawesi.
Foodplants.–– Approximately 30 families of flowering plants, the most important
being: Apiaceae, Lauraceae, Magnoliaceae, Rutaceae.
Key works.–– Hancock (1983b, 1993), Collins & Morris (1985), Miller (1987).
Chilasa Moore, [1881]

(mimes — Pl. 4, fig. 2)
Range (1+2+5+6+7).–– Oriental Region, extending east to Philippines, Sulawesi

and Lesser Sunda Islands, absent from the Moluccas, but recurs in New Guinea, Bis-
marck Archipelago and the Solomon Islands. Thirteen species recognised in two sub-
genera, of which one is restricted to China and Taiwan.
Foodplants.–– Lauraceae (Cinnamomum, Cryptocarya, Litsea).
Chilasa (Chilasa) Moore, [1881]
Range.–– As genus; 11 species in 4 groups, of which the single, endemic species

found on Sulawesi represents the veiovis-group, otherwise only known from two Phi-
lippine species (Mindanao and Leyte).
*C. (C.) veiovis Hewitson, 1865

(Sulawesi Mime — Pl. 4, fig. 2)
Range (E).–– Sulawesi (see Roos, 1995)
Papilio Linnaeus, 1758

(helens, mormons, peacocks and swallowtails — Pl. 4)
Range (W).–– Cosmopolitan; about 195 species, divided into 9 subgenera of which
three occur in the Sulawesi Region.
Note.–– Hancock (1983b) divided Papilio into six genera, with two of these divided
into two subgenera, and a third with four subgenera. Collins & Morris (1985) recogni-
sed Hancock’s six full genera as subgenera, and treated all his subgenera as syno-
nyms. The classification adopted here is that of Häuser et al. (2001), with a total of nine
subgenera, three of which occur in the Sulawesi Region.
Foodplants.–– As tribe.
Key works.–– Igarashi (1979), Tsukada & Nishiyama (1982), Hancock (1983b), Collins
& Morris (1985).
Papilio (Achillides) Hübner, [1819]

(peacocks — Pl. 4, figs 5, 8)
Range.–– About 25 species, mainly in Oriental Region, but extending into E Palae-
arctic, and eastward to Solomon Islands, Australia and New Caledonia.
Foodplants.–– Rutaceae.
*P. (A.) blumei Boisduval, 1836

(Blume’s Peacock — Pl. 4, fig. 5)
Range (E).–– Sulawesi. This outstandingly beautiful insect is an endemic mem-
ber of the palinurus-group, which comprises five species distributed from Sri Lanka
to Sumatra, Borneo and the Philippines.

Foodplants.–– Euodia, Toddalia (Rutaceae). Igarashi (1994) and Igarashi & Fukuda
(2000) illustrate larvae and pupae.
Status.–– Not known to be threatened (Collins & Morris, 1985); insufficiently
known (New & Collins, 1991).
–– *P. (A.) blumei blumei Boisduval, 1836
Range.–– Sulawesi (N, C, SE; see also Roos, 1993).
–– *P. (A.) blumei fruhstorferi Röber, 1897
P. (A.) peranthus Fabricius, 1787

(Swift Peacock — Pl. 4, fig. 8)
Range (5+6).–– Java, Bawean, Lesser Sunda Islands (to Alor), and Sulawesi
Region. The peranthus-group currently includes four species, distributed from Java to
Tanimbar, Sulawesi, the Moluccas and Irian Jaya.
Note.–– The Sulawesi Region races grouped here under peranthus are much larger
than peranthus from Java and the Lesser Sundas, and may eventually prove to repre-
sent a separate, endemic species (Collins & Morris, 1985). In northern Sulawesi this
species can often be seen flying along streams and valleys in rapid flight, but is far less
often encountered on damp sand than P. blumei.
Foodplants.–– Micromelum (Rutaceae). Early stages and hostplant illustrated from
Sulawesi by Igarashi (1979) and Igarashi & Fukuda (2000).
Status.–– not known to be threatened.
–– *P. (A.) peranthus adamantius Felder & Felder, 1864
–– *P. (A.) peranthus insulicola Rothschild, 1896
Range.–– Sulawesi (S, ?C — Kitahara, 1989), Salayar.
–– *P. (A.) peranthus subsp. (Roos, 1993)
Range.–– Sulawesi (SE).
–– *P. (A.) peranthus intermedius Snellen, 1890
Range.–– Tanahjampea, Kalao, Bonerate.
–– *P. (A.) peranthus kransi Jurriaanse & Lindemans, 1920
Range.–– Buton.
–– *P. (A.) peranthus wangiwangiensis Kitahara, 1989
Range.–– Kep. Tukangbesi (Wangiwangi)
Note.–– Kitahara (1989) did not compare his new taxon with subspecies kransi, but
only with mainland peranthus.
Papilio (Menelaides) Hübner, [1819]

(helens, mormons and swallowtails — Pl. 4, figs 1, 3, 4, 6, 7)
Range.–– Oriental and Australian Regions, slightly extending to temperate Asia.

Nearly 60 species, divided amongst 10 species-groups, 10 and 5 of which respectively
are found in the Sulawesi Region.
Foodplants.–– Rubiaceae, Rutaceae.
*P. (M.) gigon Felder & Felder, 1864

(Sulawesi Banded Swallowtail — Pl. 4, fig. 7)
Range (R).–– Sulawesi Region. One of the four members of the demolion-group,
distributed from Asia to the Papuan Region, including the Philippines but not the Les-
ser Sunda Islands.
Foodplants.–– Citrus, Euodia, Glycosmis (Rutaceae). Igarashi & Fukuda (1997) illu-
strate all life stages (see also Igarashi, 1979).
–– *P. (M.) gigon gigon Felder & Felder, 1864
Range.–– Sulawesi, Kep. Sangihe (Siao).
–– *P. (M.) gigon neriotes Rothschild, 1908
Range.–– Kep. Talaud, Kep. Sangihe (Sangihe).
–– *P. (M.) gigon mangolinus Fruhstorfer, 1899
Range.–– Kep. Banggai (Peleng), Kep. Sula (Mangole, Sanana, Taliabu).
*P. (M.) sataspes Felder & Felder, 1864

(Sulawesi Red Helen — Pl. 4, fig. 6)
Range (R).–– Sulawesi Region. Endemic representative of the helenus-group (about
eight species), found from Asia to the Philippines, Sulawesi and the Lesser Sunda
Islands, but not in the Moluccas or New Guinea.
Foodplants.–– Euodia, Micromelum, Toddalia (Rutaceae) (Igarashi & Fukuda, 2000,
who also illustrate the early stages).
–– *P. (M.) sataspes sataspes Felder & Felder, 1864
–– *P. (M.) sataspes artaphernes Honrath, 1886
Range.–– Kep. Banggai (Banggai, Peleng).
–– *P. (M.) sataspes ahasverus Staudinger, 1895
Range.–– Kep. Sula (Sanana).
P. (M.) hipponous Felder & Felder, 1862

Range (P).–– Philippines (Haugum & Collins, 1987; Treadaway, 1995), Kep.
Talaud, Kep. Sangihe, ?Sulawesi.
Foodplants.–– Citrus (Rutaceae). Ae (1977) described the early stages.
Status.–– Insufficiently known (New & Collins, 1991).
P. (M.) fuscus Goeze, 1779

(Blue Helen)
Range (3+4+5).–– Lesser Sunda Islands (including Bali), Sulawesi Region, N & C
Maluku, New Guinea region, Australia, Solomon Islands, Vanuatu. The fuscus com-
plex consists of three allopatric species (Hancock, 1983a, 1985, 1992) distributed from
Asia to Vanuatu.
Foodplants.–– Morinda (Rubiaceae); Bosistoa, Citrus, Clausena, Euodia, Fagara, Geijera,
Glycosmis, Halfordia, Microcitrus, Micromelum, Murraya, Zanthoxylum (Rutaceae). Igaras-
hi & Fukuda (2000) illustrate eggs, larvae and pupae (see also Igarashi, 1979).
–– *P. (M.) fuscus minor Oberthür, 1879

Range.–– Sulawesi (N), Kep. Sangihe (Sangihe, Siao).
–– *P. (M.) fuscus pertinax Wallace, 1865
Range.–– Sulawesi (S, SE: Roos, 1995), Kabaena. Jurriaanse & Lindemans (1920)
suggested that a separate subspecies may fly on Kabaena, but the three females in
Coll. Jurriaanse in the Leiden Museum, although variable in the extension of white on
the hindwing, do not warrant separation (see also Roos, 1995).
–– *P. (M.) fuscus lunifer Rothschild, 1895
Range.–– Kep. Talaud (Salebabu, ?Karakelong).
–– *P. (M.) fuscus porrothenus Jordan, 1909
Range.–– Sulawesi (SW), Kalao, Tanahjampea, ?Salayar.
–– *P. (M.) fuscus wasiensis Hanafusa, 1991
Range.–– Kep. Tukangbesi (Wangiwangi).
–– *P. (M.) fuscus metagenes Fruhstorfer, 1904
Range.–– Kep. Tukangbesi (Binongko).
–– *P. (M.) fuscus talyabona Joicey & Talbot, 1932
P. (M.) alphenor Cramer, 1776

(Philippine Mormon)
Range (1+2+3+4).–– Philippines (including Palawan), Palau Islands, Kep. Talaud,
Kep. Sangihe, Kep. Sula, N & C Maluku, Misool, ?New Guinea (not noted by Parsons,
1999). This and the next two species belong to the polytes-group, five species with a
combined distribution ranging from Sri Lanka to the Solomon Islands.
–– *P. (M.) alphenor perversus Rothschild, 1895 (= P. polytes alpheios Jordan, 1909, see
Moonen, 1998)
Range: Sulawesi (N), Kep. Talaud, Kep. Sangihe.
–– *P. (M.) alphenor polycritos Fruhstorfer, 1901
Range: Kep. Banggai (Peleng), Kep. Sula (Taliabu, Sanana).
P. (M.) polytes Linnaeus, 1758

(Common Mormon)
Range (5+6+7).–– Sri Lanka, India, Indo-China, China, Ryukyu Islands, Malay
Peninsula, Sumatra, Java, Lesser Sunda Islands, Borneo, Philippines (Batan Islands
only), Sulawesi Region.
Foodplants.–– Aegle, Atalantia, Citrus, Clausena, Euodia, Fortunella, Glycosmis, Micro-
melum, Murraya, Paramignya, Poncirus, Toddalia, Triphasia, Zanthoxylum (Rutaceae). Iga-
rashi (1979) and Bascombe et al. (1999) illustrate the early stages.
Status.–– Common.
–– *P. (M.) polytes alcindor Oberthür, 1879
Range.–– Sulawesi (N, C, S, SE), Kabaena, Buton, Salayar. See Moonen (1998).
–– *P. (M.) polytes tucanus Jordan, 1909
Range.–– Kep. Tukangbesi (Binongko, Kaledupa).
*P. (M.) jordani Fruhstorfer, 1906

(Jordan’s Mormon — Pl. 4, figs 3, 4)
Note.–– The females of this rare species look and fly remarkably like the danaine
Idea blanchardii (Pl. 16, fig. 2), with which they occur locally in the Minahassa Peninsu-
la (RIVW, pers. obs.).
Status.–– Listed as rare by Collins & Morris (1985), and as vulnerable by Baillie &
Groombridge (1996). See New & Collins (1991).
P. (M.) rumanzovia Eschscholtz, 1821

(Red Mormon)
Range (P).–– Philippines (excluding Balabac, and central and southern Palawan:
see Treadaway, 1995), Kep. Talaud, Kep. Sangihe (Sangihe, Siao). This and the next 2
species belong to the memnon-group, 13 species with a collective range from India to
the Philippines, Sulawesi, Moluccas and Lesser Sunda Islands.
Foodplants.–– Atalantia, Citrus (Rutaceae).
P. (M.) memnon Linnaeus, 1758

(Great Mormon)
Range (P).–– North-east India, Indo-China, China, Taiwan, southern Japan, Malay
Peninsula, Sumatra, Java, Lesser Sunda Islands (to Alor), Borneo, Kangean, Kalao,
?Maluku (?Obi: P. memnon nestor Talbot, 1929; ?Ambon).
Note.–– A recently introduced hybrid “race” of P. memnon is now widespread in C
Maluku; Andrew Rawlins, pers. comm.).
Foodplants.–– Aristolochia (Aristolochiaceae); Magnolia, Michelia (Magnoliaceae);
Atalantia, Citrus, Fortunella, Paramignya, Poncirus, Severinia, Toddalia, Zanthoxylum
(Rutaceae). Igarashi (1979) and Bascombe et al. (1999) illustrate the early stages.
Status.–– Not threatened.
–– *P. (M.) memnon kalaomemnon Hachitani, 1987
Range.–– Kalao.
*P. (M.) ascalaphus Boisduval, 1836

(Sulawesi Blue Mormon — Pl. 4, fig. 1)
Foodplants.–– Citrus (Rutaceae). Igarashi (1979) illustrates the early stages.
–– *P. (M.) ascalaphus ascalaphus Boisduval, 1836
Range.–– Sulawesi, Salayar, Buton (Fujioka et al., 1997).
–– *P. (M.) ascalaphus munascalaphus Hachitani, 1988
Range.–– Muna.
–– *P. (M.) ascalaphus fukuyamai Detani, 1983
Range.–– Kep. Banggai (Peleng) (Fujioka et al., 1997, record material from Peleng
as nominate subspecies).
–– *P. (M.) ascalaphus ascalon Staudinger, 1895
Papilio (Princeps) Hübner, [1807]

(swallowtails — not illustrated)
Range.–– 19 Species divided amongst 6 species groups. Afrotropical except one

invasive species occurring from the Arabian Peninsula eastward through the Orien-
tal and Australian Regions, and into the Pacific (Hawaii and possibly other Pacific
islands).
Foodplants.–– As genus, but not including Apiaceae.
P. (Pr.) demoleus Linnaeus, 1758

(Lime, Lemon, or Chequered Swallowtail)
Range (1+2+5+6+7).–– Arabia, Afghanistan, Oriental and Australian Regions,
including Malay Peninsula, Sumatra, Java (Kato, 1989; sporadic introduction? - see
Moonen, 1991), Lesser Sunda Islands, Borneo (Otsuka, 1988), Palawan, Philippines,
Irian Jaya (Moonen, 1999), Australia (Braby, 2000) and Papua New Guinea (Parsons,
1999; Igarashi & Fukuda, 2000), but absent from Maluku. In the Sulawesi Region,
found in Kep. Sula, Kep. Sangihe, Kep. Talaud and, most recently, N Sulawesi. The
other four species belonging to the demoleus-group occur in the Afrotropical Region,
three being Madagascan endemics.
Foodplants.–– Cullen (Australia; Braby, 2000; previously included in Psoralea),
Psoralea (Fabaceae); Fagraea (Loganiaceae); Michelia (Magnoliaceae); Ziziphus (Rham-
naceae); Acronychia, Aegle, Atalantia, Chloroxylon, Citrus (cultivars!), Clausena, Flinder-
sia, Fortunella, Glycosmis, Limonia, Microcitrus, Micromelum, Murraya, Ruta, Zanthoxylum
(Rutaceae). Igarashi (1979) illustrates all life stages.
–– P. (Pr.) demoleus libanius Fruhstorfer, 1908
Range.–– Taiwan, Philippines (including Palawan), Kep. Talaud, Kep. Sangihe
(Sangihe; F. Kodong, pers. comm., 1988), Kep. Sula (Sanana), and Manado district of
N Sulawesi, where it is now common (F. Kodong, pers. comm., 2002).
Leptocircini Kirby, 1896 (= Graphiini, = Lampropterini)

(kites, triangles, jays, swordtails and dragontails — Pl. 5)
Range.–– Pantropics, with extensions into temperate regions; about 150 species in
7 genera, only 2 of which occur in the Sulawesi Region.
Foodplants.–– Primarily Annonaceae; also Lauraceae, Rosaceae.
Morris (1985), Miller (1987).
Graphium Scopoli, 1777

(kites, triangles, jays and swordtails — Pl. 5, figs 1-6)
Range (W).–– Palaeotropics, with weak extensions to temperate regions. About

100 species in 5 subgenera, 3 of which occur in Sulawesi.
Foodplants.–– Predominantly Annonaceae and Lauraceae; also ?Apocynaceae,
Aquifoliaceae, Atherospermataceae, Euphorbiaceae, Hernandiaceae, Magnoliaceae,
Monimiaceae, Myrtaceae, Rutaceae, Sapotaceae, Winteraceae.

Key works.–– Saigusa et al. (1982), Tsukada & Nishiyama (1982), Collins & Morris
(1985), Miller (1987), Hancock (1993).
Graphium (Graphium) Scopoli, 1777

(Pl. 5, figs 2-4, 6)
Range.–– Indo-Australian region, extending to Japan. About 28 species (6 in Sula-

wesi) in 5 species groups (3 in Sulawesi).
Foodplants.–– Range similar to genus.
G. (G.) codrus Cramer, 1779

(Eastern Olive Triangle — Pl. 5, fig. 6)
Range (2+3+4).–– Philippines (excluding Palawan), Sulawesi Region, N & C Malu-
ku, New Guinea region, Solomon Islands. This and the next two species are members
of the sarpedon-group, ten species with a combined widespread distribution from Sri
Lanka to Japan, New Caledonia and Tasmania. G. empedovana Corbet, which occurs
throughout the Greater Sundas, is sometime included as a subspecies of codrus (see
Collins & Morris, 1985).
Foodplants.–– Annona, Uvaria (Annonaceae); Hernandia (Hernandiaceae); ?Thespesia
(Malvaceae). Igarashi (1979) and Igarashi & Fukuda (2000) illustrate larvae and pupae.
–– *G. (G.) codrus celebensis Wallace, 1865
Range.–– Sulawesi, Kep. Banggai (Peleng).
–– *G. (G.) codrus taloranus Jordan, 1909
Range.–– Kep. Talaud.
–– *G. (G.) codrus stiris Jordan, 1909
*G. (G.) monticolus Fruhstorfer, 1896

(Sulawesi Blue Triangle — Pl. 5, fig. 4)
Note.–– Long treated as a subspecies of G. sarpedon, separation as a montane Sulawe-
si endemic appears justified (d’Abrera, 1982; Roos, 1993; Moonen, 1998; Parsons, 1999).
Foodplants.–– According to Toxopeus (1950), can be bred on (literally) the same
plant as G. anthedon milon - unfortunately he did not say what it was! Based on Igaras-
hi & Fukuda (2000), possibly Cinnamomum (Lauraceae).
–– *G. (G.) monticolus textrix Tsukada & Nishiyama, 1980 (= longilinea Joicey & Talbot,
1922; = longilineatus Toxopeus, 1950; unavailable names)
Note.–– d’Abrera (1982) regarded this as a straight synonym of monticolus, but the
work of Toxopeus (1950) indicates that this is not the case. Superficial examination of
museum material even suggests that the two taxa could represent separate species.
–– *G. (G.) monticolus monticolus Fruhstorfer, 1896
G. (G.) anthedon Felder & Felder, 1864 (= milon)

(Wallacea Bluebottle)
Note.–– This species was long treated as a subspecies of G. sarpedon. Tsukada &
Nishiyama (1980) recognised it as separate, under the name G. milon Felder & Fel-
der, 1865, but this name is junior to anthedon Felder & Felder, 1864 (Kirby, 1871;
Moonen, 1998). Application of Article 23.9 (ICZN, 1999) to conserve the use of milon
by giving it precedence over anthedon does not appear justifiable, given the relative
obscurity of this taxon.
Foodplants.–– Cinnamomum (Lauraceae). Igarashi & Fukuda (2000) illustrate food-
plant and early stages (as G. milon).
–– *G. (G.) anthedon milon Felder & Felder, 1865
Range.–– Sulawesi, Kep. Talaud, Kabaena, Buton, Kep. Banggai (Peleng). Fujioka et
al. (1997) include material from Peleng and Kep. Sangihe in the following subspecies.
–– *G. (G.) anthedon coelius Fruhstorfer, [May] 1899 (= sulaensis Lathy, June 1899)
Range.–– Kep. Sula (Mangole, Sanana, Taliabu: Moonen, 1998).
G. (G.) eurypylus Linnaeus, 1758

(Pale Green Triangle, or Great Jay)
Range (W).–– Northern India, Indo-China, China, Malay Peninsula, Sumatra, Java,
Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region, Maluku, New
Guinea region, Australia. This and the next species belong to the eurypylus-group,
nine species which together have a widespread distribution extending from Sri Lanka
to Japan, New Guinea and northern Australia.
Foodplants.–– Annona (also on introduced and cultivated species), Artabotrys,
Desmos, Fitzalania, Melodorum, Miliusa, Mitrephora, Polyalthia, Pseuduvaria, Rauwenhof-
fia, Saccopetalum, Uvaria (Annonaceae); in Thailand on Michelia (Magnoliaceae); in
Australia also found on introduced Magnolia (Magnoliaceae). Igarashi & Fukuda
(2000) illustrate eggs, larvae and pupae.
–– *G. (G.) eurypylus pamphylus Felder & Felder, 1865
–– *G. (G.) eurypylus sangira Oberthür, 1879
–– G. (G.) eurypylus gordion Felder & Felder, 1864
Range.–– Philippines, Kep. Talaud.
–– *G. (G.) eurypylus insularis Rothschild, 1896
Range.–– Salayar, Kalao, Tanahjampea.
–– *G. (G.) eurypylus fumikoe Detani, 1983
–– *G. (G.) eurypylus arctofasciatus Lathy, 1899.
*G. (G.) meyeri Hopffer, 1874

(Meyer’s Triangle — Pl. 5, fig. 2)
–– *G. (G.) meyeri meyeri Hopffer, 1874
Range.–– Sulawesi (see Roos, 1993), Kep. Banggai (Peleng).
–– *G. (G.) meyeri extremum Tsukada & Nishiyama, 1980
G. (G.) agamemnon Linnaeus, 1758

(Green-spotted Triangle, or Tailed Jay — Pl. 5, fig. 3)
Range (W).–– Sri Lanka, India, southern China, Indo-China, Malay Peninsula,
Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi
Region, Maluku, New Guinea region, Solomon Islands, northern Australia. G. aga-
memnon is the only widespread member of the agamemnon-group of subgenus Grap-
hium, the other six members being completely restricted to the Papuan Region, to
the east of Weber’s Line.
Foodplants.–– Ancana, Annona (also on introduced and cultivated species), Arta-
botrys, Cyathostemma, Desmos, Fissistigma, Fitzalania, Goniothalamus, Guatteria, Haplo-
stichanthus, Meiogyne, Melodorum, Miliusa, Mitrephora, Oncodostigma, Polyalthia, Pseu-
duvaria, Rauwenhoffia, Rollinia, Uvaria, Xylopia (Annonaceae); Durio (Bombacaceae);
Dioscorea (Dioscoreaceae); Cassia (Fabaceae); Cinnamomum, Cryptocarya (Lauraceae);
Elmerillia, Magnolia, Michelia (Magnoliaceae); Piper (Piperaceae); Citrus (Rutaceae).
Igarashi & Fukuda (2000) illustrate the early stages; see also Igarashi (1979) and Bas-
combe et al. (1999).
–– *G. (G.) agamemnon comodus Fruhstorfer, 1903
Range.–– Throughout Sulawesi Region.
Graphium (Pathysa) Reakirt, 1865

(swordtails and zebras — Pl. 5, fig. 5)
Range.–– Oriental and Australian Regions. Collins & Morris (1985) recognised 23
species in two species groups, the antiphates group and the macareus group. These
groups are recognised here as subgenus Pathysa and subgenus Paranticopsis, respecti-
vely. Pathysa includes about a dozen species, five of which occur in Sulawesi.
Foodplants.–– Annonaceae, Lauraceae, Magnoliaceae.
*G. (Pat.) rhesus Boisduval, 1836

(Monkey Swordtail)
–– *G. (Pat.) rhesus rhesus Boisduval, 1836
Range.–– Sulawesi (N, ?C, E, SE — see Roos, 1993), Buton.
–– *G. (Pat.) rhesus rhesulus Fruhstorfer, 1902
Range.–– Sulawesi (?C, S), Kep. Banggai (Peleng).
–– *G. (Pat.) rhesus rhapia Jordan, 1908

Range.–– Tanahjampea, Kep. Tukangbesi.
–– *G. (Pat.) rhesus subsp. (Okano, 1988)
Range.–– Kalao.
–– *G. (Pat.) rhesus parvimacula Joicey & Talbot, 1922
Range.–– Kep. Sula (Sanana, Mangole).
*G. (Pat.) androcles Boisduval, 1836

(Lion Swordtail)
–– *G. (Pat.) androcles androcles Boisduval, 1836
Range.–– Sulawesi (see Roos, 1993).
–– *G. (Pat.) androcles pelengensis Detani, 1983
–– *G. (Pat.) androcles cleomenes Fruhstorfer, 1911
*G. (Pat.) dorcus de Haan, 1840

(Tabitha’s Swordtail — Pl. 5, fig. 5)
Range (R).–– Sulawesi, Buton.
Status.–– Insufficiently known (Collins & Morris, 1985; New & Collins, 1991).
–– *G. (Pat.) dorcus dorcus de Haan, 1840
Range.–– Sulawesi (N; see Haugum, 1988).
–– *G. (Pat.) dorcus ventus Tsukada & Nishiyama, 1980
–– *G. (Pat.) dorcus butungensis Hanafusa, 1997
Range.–– Buton.
G. (Pat.) antiphates Cramer, 1775

(Five-bar Swordtail)
Range (5+6+7).–– Sri Lanka, southern and northern India, Indo-China, China,
Malay Peninsula, Sumatra, Java, Lesser Sunda Islands, Borneo, southern Sulawesi
Region.
Foodplants.–– Annona, Desmos, Goniothalamus, Melodorum, Miliusa, Uvaria, Xylopia
(Annonaceae); Michelia (Magnoliaceae). Igarashi & Fukuda (2000) illustrate the early
stages.
–– *G. (Pat.) antiphates kurosawai Igarashi, 1979
Range.–– Sulawesi (C, S).
–– G. (Pat.) antiphates kalaoensis Rothschild, 1896
Range.–– Lesser Sunda Islands (Lombok to Alor), Kalao, Tanahjampea.
G. (Pat.) euphrates Felder & Felder, 1862

(Euphrates Swordtail)
Range (1+2+3).–– Banggi (small island between Borneo and Balabac), Balabac,
Palawan, Philippines, Sulawesi, N Maluku (Halmahera and Bacan: Andrew Rawlins,

pers. comm.). See Tsukada & Nishiyama (1982), Page (1987).
Foodplants.–– Lauraceae.
–– *G. (Pat.) euphrates elegantia Tsukada & Nishiyama, 1980
Graphium (Paranticopsis) Wood-Mason & de Nicéville, 1887

(zebras — Pl. 5, fig. 1)
Range.–– Oriental and Australian Regions. Only two species of this group (inclu-
ding one of the two species in Sulawesi) are found east of the Wallace Line. These eas-
tern species do not occur beyond New Guinea. Collins & Morris (1985) distinguished
the 12 species involved as the macareus group of the subgenus Pathysa.
Foodplants.–– Aquifoliaceae (Hancock, 1983b).
*G. (Par.) encelades Boisduval, 1836

(Sulawesi Zebra)
Range (R).–– Sulawesi, Kep. Banggai (Peleng). Moonen (1998) illustrates the female.
G. (Par.) deucalion Boisduval, 1836

(Yellow Zebra — Pl. 5, fig. 1)
Range (3).–– Sulawesi, Kep. Banggai, northern Maluku, Biak (Irian Jaya).
Note.–– Inclusion of the Biak population (felixi Joicey & Noakes) within G. deuca-
lion follows the novel suggestion of Hancock (1979), but Parsons (1999) appears to
retain felixi as a subspecies of G. thule Wallace (from Waigeo and New Guinea).
–– *G. (Par.) deucalion deucalion Boisduval, 1836
–– *G. (Par.) deucalion marabuntana Detani, 1983
Lamproptera Gray, 1832

(dragontails — Pl. 5, fig. 7)
Range (1+2+6+7).–– Northeastern Indian Region, Indo-China and southern China

south to Sumatra, Java, Philippines and Sulawesi Region. Two species only; both occur
together throughout much of their range, except that L. meges, the species found in Sula-
wesi, exceeds the range of L. curius by extending through the Philippines proper to Sula-
wesi and Kep. Banggai.
Foodplants.–– Hernandiaceae.
Key works.–– Tsukada & Nishiyama (1982), Collins & Morris (1985).
L. meges Zinken, 1831

(Green Dragontail — Pl. 5, fig. 7)
Range (1+2+6+7).–– Assam, Indo-China, Hainan, Malay Peninsula, Sumatra, Java,
Borneo, Palawan, Philippines, Sulawesi.

Foodplants.–– Illigera (Hernandiaceae). In the Philippines also recorded from Zan-
thoxylum (Rutaceae). Igarashi & Fukuda (2000) illustrate eggs, larvae and pupae.
Status.–– Not known to be threatened (in Indonesia).
–– *L. meges ennius Felder & Felder, 1865
Range.–– Sulawesi (N, C, S, SE; see also Roos, 1993), Kep. Banggai (Peleng).
–– *L. meges akirai Tsukada & Nishiyama, 1980
Pieridae Swainson, 1831

(whites and sulphurs)
Range.–– Cosmopolitan (about 1200 species, 60 genera); two major subfamilies

(both represented in Sulawesi), and two minor subfamilies (both unrepresented in the
Oriental and Australian Regions).
Foodplants.–– More than 30 families of flowering plants, but primarily Asteraceae,
Brassicaceae, Capparaceae, Fabaceae, Loranthaceae, Rhamnaceae, Santalaceae and
Zygophyllaceae; Coniferales (one American genus).
Key works.–– Klots (1933), d’Abrera (1982), Corbet & Pendlebury (1992), Common
& Waterhouse (1981), Yata (1981a), Bridges (1988a), Ackery (1989), Peggie et al. (1995).
Coliadinae Swainson, 1821

(sulphurs, yellows — Pl. 6, figs 2, 6, 14)
Range.–– Cosmopolitan; more than 200 species, in about a dozen genera.

Foodplants.–– Primarily Asteraceae, Fabaceae, Rhamnaceae and Zygophyllaceae;
never Brassicaceae or Loranthaceae, a few records of Capparaceae.
Gandaca Moore, 1906

(tree yellows — Pl. 6, fig. 6)
Range (W).–– Oriental and Australian Regions, from Sikkim to New Guinea. For-
merly treated as monobasic, Yata (1981a) recognised two allopatric species, with the
Sulawesi Region populations belonging to the eastern taxon, while the distinctive but
more easterly Kep. Banggai and Kep. Sula population belongs to the western taxon
(Yamauchi & Yata, 2000). As Yamauchi & Yata point out, such a doubly disjunct dis-
tribution is unique.
Foodplants.–– Annonaceae (Monocarpia, Mitrephora); Connaraceae (Connarus);
Rhamnaceae (Ventilago).
Key works.–– Corbet & Pendlebury (1992), Yata (1981a), Yamauchi & Yata (2000).
G. butyrosa Butler, 1875

(Eastern Tree Yellow — Pl. 6, fig. 6)
Range (2+3+4).–– S Philippines (Dinagat, Mindanao), Sulawesi, N & C Maluku,
Aru, Waigeo, New Guinea. Whether or not both species are truly sympatric in parts of
S Philippines remains uncertain (Yamauchi & Yata, 2000).
–– *G. butyrosa samanga Fruhstorfer, 1910

G. harina Horsfield, 1829

(Tree Yellow)
Range (P).–– Eastern India, southern China, Andamans, Peninsula Malaya, Suma-
tra, Java, Lesser Sundas, Borneo, Palawan, N & S Philippines, Kep. Banggai, Kep. Sula.
Foodplants.–– Mitrephora, Monocarpia (Annonaceae); Connarus (Connaraceae); Ven-
tilago (Rhamnaceae). Igarashi & Fukuda (2000) illustrate the life history.
–– *G. harina auriflua Fruhstorfer, 1898
Range.–– Kep. Banggai (Peleng), Kep. Sula (Mangole, Sanana, Taliabu). Yam-
auchi & Yata (2000) speculate that Gandaca from N Sulawesi could also possibly
belong to harina, but they were unable to obtain material from Sulawesi Utara for
examination.
Eurema Hübner, 1819

(grass yellows — Pl. 6, fig. 2)
Range (W).–– Cosmotropical, extending weakly into temperate regions. A large

genus with well over 60 species (about half of which occur in the Old World) and cur-
rently divided into just two subgenera, both represented in Sulawesi.
Foodplants.–– Apocynaceae, Asteraceae, Connaraceae, Cucurbitaceae, Euphor-
biaceae, Fabaceae, Hypericaceae, Osmundaceae, Palmae, Rhamnaceae, Rubiaceae,
Santalaceae, Simaroubaceae, Theaceae, Verbenaceae.
Key works.–– Holloway (1973), Corbet & Pendlebury (1992), Common & Water-
house (1981), Yata (1981a, 1988, 1989, 1991, 1992, 1994, 1995).
Eurema (Eurema) Hübner, 1819
Range.–– As genus but primarily Neotropical, with only four Old World species.
Of these, one is purely Afrotropical and another is Australian. Of the two species
widespread in the Indo-Australian tropics, only one occurs on Sulawesi.
E. (E.) brigitta Stoll, 1780

(No-brand Grass Yellow)
Range (2+3+4+5+6+7).–– palaeotropics, from West Africa to Madagascar, Sri
Lanka, China and Taiwan, Malay Peninsula, Sumatra, Java, Borneo (Otsuka, 1991),
Philippines (Luzon, Mindanao, Siquijor: only in clearings - see Treadaway, 1995), Les-
ser Sunda Islands, Sulawesi, Palau islands, northern and central Maluku to New Gui-
nea, eastern Australia and Fiji.
Foodplants.–– Adenanthera, Albizia, Cassia, Chamaecrista, Desmodium, Erioglossum,
Neptunia, Pithecolobium , Senna, Sesbania (Fabaceae); Hypericum (Hypericaceae). The life
history has been described by Bascombe et al. (1999) for the Hong Kong population,
and by Henning et al. (1997) for southern Africa.
–– *E. (E.) brigitta ina Eliot, 1956
Range.–– Sulawesi, Muna. Yata (1989) gives S. Sulawesi only.
Eurema (Terias) Swainson, 1821
Range.–– Palaeotropics, particularly the Oriental Region. Nearly 30 species, divi-

ded by Yata (1988, 1989) into 5 species groups; Sulawesi has 6 species, representing 2
of these groups.
E. (T.) hecabe Linnaeus, 1758

(Common Grass Yellow)
Range (W).–– Palaeotropics, from West Africa to Japan, Malay Peninsula, Sumatra,
Maluku, New Guinea, eastern Australia, Solomons, New Caledonia, Fiji, etc. This and
the next three species all belong to the hecabe-group, an assemblage totalling eight spe-
cies with a collective distribution comparable to the subgenus as a whole.
Foodplants.–– Alstonia (Apocynaceae); Solidago (Asteraceae); Connarus (Conna-
raceae); Bryonia (Cucurbitaceae); Breynia, Bridelia, Phyllanthus (Euphorbiaceae); Abrus,
Acacia, Aeschynomene, Albizia, Alstonia, Arachis, Archidendron, Caesalpinia, Cassia, Cha-
maecrista, Delonix, Entada, Galactia, Gleditsia, Indigofera, Kummerowia, Lespedeza, Leucae-
na, Macrotropis, Medicago, Mimosa, Moullava, Ormocarpum, Paraserianthes, Parkia, Pithe-
cellobium, Pterocarpus, Robinia, Senna, Sesbania, Smithia, Trigonella, Wagatea (Fabaceae);
Cratoxylon (Hypericaceae); Osmunda (Osmundaceae); Cocos (Palmae); Phyllanthus,
Rhamnus, Sageretia, Ventilago (Rhamnaceae); Coffea (Rubiaceae); Santalum (Santalace-
ae); Camellia (Theaceae); Tectona (Verbenaceae). Igarashi & Fukuda (2000) illustrate
egg, larva and pupa.
–– *E. (T.) hecabe latimargo Hopffer, 1874
Range.–– Sulawesi (N, C), Buton, Muna. According to Yata (1995), “this subspecies
is restricted to North and West Sulawesi”.
–– *E. (T.) hecabe sinda Fruhstorfer, 1910
–– *E. (T.) hecabe pylos Fruhstorfer, 1910
Range.–– Kep. Banggai (Banggai, Peleng), Kep. Sula (Mangole, Sanana).
–– *E. (T.) hecabe dentyris Fruhstorfer, 1910
Range.–– Salayar, Tanahjampea. According to Yata (1995), the type specimen of
dentyris may represent E. alitha (subspecies djampeana); the correct placement of mate-
rial from Salayar now seems open to doubt - it may also belong to alitha.
–– *E. (T.) hecabe kalidupa Fruhstorfer, 1910
Range.–– Kep. Tukangbesi (Kaledupa, Tomea; Yata, 1995, gives only Kaledupa).
E. (T.) alitha Felder & Felder, 1862

Range (W).–– Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippi-
nes, Taiwan, Sulawesi Region, N & C Maluku, New Guinea. The work of Kitamura
(1996) suggests that true alitha may not extend further north than Mindanao in the
Philippines.
Foodplants.–– Albizia, Cassia, Desmanthus, Entada, Galactia, Glycine, Ormocarpum,
Pithecellobium, Senna (Fabaceae); Rhamnus (Rhamnaceae). The early stages are illustra-
ted by Igarashi & Fukuda (2000).
–– *E. (T.) alitha zita Felder & Felder, 1865

Range.–– Sulawesi (N, C), Kep Banggai (Peleng), ?Kep. Sula (Yata, 1988, 1995).
–– *E. (T.) alitha lorquini Felder & Felder, 1865
–– *E. (T.) alitha subsp. (Jurriaanse & Lindemans, 1920)
Range.–– Sulawesi (SE), Kabaena, Muna, Masalaka, Buton, Kep. Tukangbesi (Kale-
dupa, Tomea).
Note.–– Yata (1995) does not list alitha from these islands.
–– *E. (T.) alitha sangira Fruhstorfer, 1910
Range.–– Kep. Sangihe (Sangihe).
–– *E. (T.) alitha subsp. (ZSBS, de Jong in litt.)
Range.–– Salayar. Yata (1995) does not list E. alitha from Salayar.
–– *E. (T.) alitha djampeana Fruhstorfer, 1908
E. (T.) blanda Boisduval, 1836

(Three-spot Grass Yellow)
Range (W).–– Oriental and Australian Regions, from Sri Lanka to Solomons, inclu-
ding Indo-China, Malay Peninsula, Sumatra, Java, Lesser Sunda Islands, Borneo, Pala-
wan, Philippines, Sulawesi Region, N & C Maluku and New Guinea.
Foodplants.–– Alstonia (Apocynaceae); Acacia, Acrocarpus, Agati, Albizia, Alstonia,
Archidendron, Caesalpinia, Cassia, Delonix, Gelditsia, Gliricidia, Guilandina, Macrotropis,
Moullava, Ormosia, Parkia, Paraserianthes, Pithecellobium, Senna, Sesbania, Wagatea, Xylia
(Fabaceae); Camellia (Theaceae), Agatea (Violaceae). Igarashi & Fukuda (2000) illustrate
eggs, larvae and pupae.
–– *E. (T.) blanda norbana Fruhstorfer, 1910
Range.–– Sulawesi (N, C), Kep. Talaud (Peggie et al., 1995 - but Yata, 1994, does
not mention Talaud), Kep. Sangihe (Yata, 1994), Kep. Banggai (Peleng), Kep. Sula
(Mangole, Sanana).
–– *E. (T.) blanda odinia Fruhstorfer, 1910
Range.–– Sulawesi (S), Buton (but Yata, 1994, does not mention Buton).
*E. (T.) irena Corbet & Pendlebury, 1932

Note.–– Formally raised to full species status by Yata (1994).
*E. (T.) celebensis Wallace, 1867

Range (R).–– Sulawesi Region. This and the next species belong to the sari-group,
18 species restricted to the Indo-Australian region.
–– *E. (T.) celebensis celebensis Wallace, 1867
Range.–– Sulawesi, ?Kep. Sangihe.
Note.–– According to Yata (1991), the nominate race is confined to the main island
of Sulawesi - he does give any record of the species from Kep. Sangihe.
–– *E. (T.) celebensis exophthalma Fruhstorfer, 1910
Range.–– Kep Banggai (Peleng), Kep. Sula (Mangole, Sanana).
E. (T.) tominia Vollenhoven, 1865

(Pl. 6, fig. 2)
Range (7).–– Borneo, Sulawesi Region.
Foodplants.–– Yata (1992) cites old literature indicating that the hostplant is a tall
tree belonging to the Fabaceae.
–– *E. (T.) tominia tominia Vollenhoven, 1865
–– *E. (T.) tominia theristra Fruhstorfer, 1911
–– *E. (T.) tominia talissa Westwood, 1888
Range.–– Talisei, Kep. Sangihe (Siao).
–– *E. (T.) tominia halesa Fruhstorfer, 1910
–– *E. (T.) tominia arsia Fruhstorfer, 1910
Range.–– Tanahjampea and Kalao (Yata 1992).
–– *E. (T.) tominia faunia Fruhstorfer, 1910
Range.–– Kep. Tukangbesi (?Kaledupa, ?Tomea).
–– *E. (T.) tominia mangolina Fruhstorfer, 1910
Range.–– Kep Banggai (Peleng), Kep. Sula (Mangole, Sanana; Yata, 1992, adds
?Taliabu).
Catopsilia Hübner, 1819

(emigrants — Pl. 6, fig. 14)
Range (W).–– Palaeotropics. Four species in the Indo-Australian region, all wides-
pread and found on Sulawesi except one confined to Australia.
Foodplants.–– Fabaceae; there are scattered records on Araceae, Capparaceae and
Thymelaeaceae.
Key works.–– Corbet & Pendlebury (1992), Common & Waterhouse (1981), Yata
(1981a).
C. scylla Linnaeus, 1763

(Orange Emigrant)
Range (W).–– Burma, Malay Peninsula, Sumatra, Java, Lesser Sunda Islands, Bor-
neo, Palawan, Philippines, Sulawesi Region, N & C Maluku, ?New Guinea, Bismarcks,
northern Australia, New Caledonia and Fiji.
Foodplants.–– Crateva (Capparaceae); Cassia, Senna, Tephrosia (Fabaceae). Igaras-
hi & Fukuda (1997) illustrate larva and pupa.
–– C. scylla asema Staudinger, 1885
Range.–– central and southern Philippines, Sulawesi, Salayar, Kalao, Kabaena,
Buton, Kep. Tukangbesi (Kaledupa).
–– *C. scylla bangkejana Fruhstorfer, 1903
Range.–– Kep. Banggai (Peleng), Kep. Sula (Sanana).
C. pyranthe Linnaeus, 1758

(Mottled Emigrant)
Range (1+2+4+5+6+7).–– Oriental and Australian Regions, from Sri Lanka to Tai-
wan, Malay Peninsula, Sumatra, Java, western Lesser Sunda Islands, Borneo, Pala-
wan, Philippines, Sulawesi Region, C Maluku (Yata, 1981a; Peggie et al., 1995), Solo-
mon Islands, New Caledonia, northern and eastern Australia. Not recorded from
New Guinea.
Foodplants.–– Colocasia (Araceae); Crateva (Capparaceae); Cassia, Crotalaria, Ormo-
carpum, Paraserianthes, Senna, Sesbania (Fabaceae); Gnidia (Thymelaeaceae). Igarashi &
Fukuda (1997) illustrate the early stages.
–– C. pyranthe pyranthe Linnaeus, 1758
Range.–– Sri Lanka, India, Indo-China, southern China, Malay Peninsula, Suma-
tra, Java, Lesser Sunda Islands, Borneo, Philippines, Sulawesi, Kep. Sula (Sanana),
Maluku (Seram, Ambon).
C. pomona Fabricius, 1775

(Lemon Emigrant — Pl. 6, fig. 14)
Range (W).–– Sri Lanka, India, Indo-China, southern China, Malay Peninsula,
Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region,
Maluku, New Guinea region, Solomon Islands, New Caledonia, Australia.
Foodplants.–– Bauhinia, Brownea, Butea, Cassia, Pterocarpus, Senna, Sesbania (Fabace-
ae). Igarashi & Fukuda (1997) illustrate the early stages.
–– *C. pomona flava Butler, 1869
Range.–– Sulawesi, Salayar, Tanahjampea, Kalao, Kabaena, Muna (Galla), Buton,
Kep. Tukangbesi (Tomea), Kep. Banggai (Peleng).
–– *C. pomona dionysiades Fruhstorfer, 1911
Range.–– Kep. Talaud, Kep. Sangihe (Sangihe, Siao).
–– C. pomona rivalis Fruhstorfer, 1910
Range.–– Kep. Sula (Mangole, Sanana), N & C Maluku, New Guinea region, Solo-
mon Islands, Vanuatu, New Caledonia, Australia.
Pierinae Swainson, 1831 (1821)

(whites, orange tips, jezebels — Pl. 6, figs 1, 3-5, 7-13)
Range.–– Cosmopolitan; about 900 species in more than 50 genera.

Foodplants.–– Primarily Brassicaceae, Capparaceae, Euphorbiaceae, Loranthaceae,
Resedaceae, Santalaceae, Tropaeolaceae; very rarely Fabaceae, Rhamnaceae, Asterace-
ae or Zygophyllaceae.
Hebomoia Hübner, 1819

(giant orange tips — Pl. 6, fig. 5)
Range (W).–– Oriental Region, eastwards to Lesser Sunda Islands, Philippines,

Sulawesi Region and Maluku. Despite the superficial resemblance to Ixias and Colotis,
Klots (1933) considered Hebomoia to be unrelated to these genera. Two species are cur-
rently recognised, one predominantly western and widespread, represented on Sula-
wesi, the other eastern, being restricted to central Maluku and eastern Sulawesi
Region (Kep. Banggai).
Foodplants.–– Brassicaceae, Capparaceae.

Key works.–– Yata (1981a).
H. glaucippe Linnaeus, 1758

(Great Orange Tip — Pl. 6, fig. 5)
Range (1+2+3+5+6+7).–– Sri Lanka, India, Indo-China, China, Ryukyu Islands,
Malay Peninsula, Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines,
Sulawesi Region, northern Maluku.
Foodplants.–– Brassica (Brassicaceae); Capparis, Crateva (Capparaceae). Igarashi &
Fukuda (1997) illustrate the early stages.
–– *H. glaucippe celebensis Wallace, 1863
Range.–– Sulawesi, Kep. Talaud, Salayar, Kalao, Tanahjampea, Buton, Kep. Bang-
gai (Peleng).
–– *H. glaucippe uedai Morita, 1996
Range.–– Kep. Banggai (Salue Is.).
–– *H. glaucippe sangirica Fruhstorfer, 1911
–– *H. glaucippe sulaensis Fruhstorfer, 1908
H. leucippe Cramer, 1775

Range (P).–– Kep. Banggai, central Maluku.
–– *H. leucippe detanii Nishimura, 1983
Pareronia Bingham, 1907

(wanderers — Pl. 6, fig. 1)
Range (W).–– Mainly Oriental Region, from Sri Lanka to the Philippines and Flo-
res, but with two species in the Moluccas, one of which (or a separate species) also
occurs on Biak. A genus of about a ten species, represented in the Sulawesi Region by
a single but highly polytypic endemic.
Foodplants.–– Capparaceae (Capparis).
Key works.–– Corbet & Pendlebury (1992), Yata (1981a).
–– *P. tritaea Felder & Felder, 1859
(Pl. 6, fig. 1)
Foodplants.–– As genus. Igarashi & Fukuda (2000) illustrate the early stages.
–– *P. tritaea tritaea Felder & Felder, 1859
Range.–– Sulawesi (N, C), Bangka.
–– *P. tritaea bargylia Fruhstorfer, 1910
Range.–– Sulawesi (S, SE).
–– *P. tritaea bilinearis Fruhstorfer, 1910
–– *P. tritaea octaviae Snellen, 1894
Range.–– Tanahjampea, Kalao.
–– *P. tritaea binongkoensis Hanafusa, 1998

Range.–– Binongko.
–– *P. tritaea illustris Hanafusa, 1991
Range.–– Kep. Tukangbesi (Wangiwangi).
–– *P. tritaea subsp.
Range.–– Batuata (Hanafusa, 1998)
–– *P. tritaea sarasinorum Martin, 1913
Range.–– Kabaena, Muna, Buton.
–– *P. tritaea hermocinia Fruhstorfer, 1910
–– *P. tritaea sulaensis Joicey & Talbot, 1926
Range.–– Kep. Sula.
Ixias Hübner, 1819

(Indian, or small orange tips — Pl. 6, fig. 4)
Range (1+2+5+6+7).–– Oriental Region eastwards to Lesser Sunda Islands, Phi-

lippines and Sulawesi. A medium-sized genus of about 16 species, considered by
Klots (1933) to be very closely related to the primarily Afrotropical Colotis. Repre-
sented in Sulawesi, at the eastern limit of the distribution of the group, by two allo-
patric endemics.
Foodplants.–– Capparaceae (Capparis, Crateva).
Key works.–– Gabriel (1943), Holloway (1973), Yata (1981a).
*I. piepersi Snellen, 1878

*I. paluensis Martin, 1914

(Pl. 6, fig. 4)
Leptosia Hübner, 1818

(spirits — Pl. 6, fig. 9)
Range (1+2+5+6+7).–– Afrotropical and Oriental Regions, eastwards to Lesser

Sunda Islands, Philippines and Sulawesi; about half a dozen species. According to
Klots (1933) this genus of exceptionally fragile butterflies is very isolated, with no
obvious close relatives. As such, it is notable that it occurs in the Lesser Sunda Islands
and western Wallacea, but has not been found in Kep. Banggai, Kep. Sula, Maluku or
further east. Corbet & Pendlebury (1992) speculate that the wide distribution of nina,
the principal Oriental species (which might only be a subspecies of the African L. alce-
sta), could have been influenced by man’s cultivation of the larval foodplants. The
presence of two supposedly distinct species on Sulawesi appears to conflict with this
idea but, as the two Sulawesi Region species are allopatric, the separate status of the
endemic must itself be open to doubt.
Foodplants.–– Capparaceae, ?Rhamnaceae.
Key works.–– Corbet & Pendlebury (1992), Yata (1981a).
L. nina Fabricius, 1793

(Psyche)
Range (1+2+5+6+7).–– Sri Lanka, India, Indo-China, China, Malay Peninsula,
Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region.
Foodplants.–– Capparis, Cleome, Crateva, Polanisia (Capparaceae); ?Rhamnus (Rham-
naceae). Foodplants and early stages illustrated by Igarashi & Fukuda (1997, 2000).
–– *L. nina dione Wallace, 1867
Range.–– Sulawesi (S, SE), Buton, Kabaena, Muna (Galla).
–– *L. nina aebutia Fruhstorfer, 1910
–– *L. nina subsp. (Jurriaanse & Lindemans, 1920)
Range.–– Kep. Tukangbesi (Binongko, Tolandono).
*L. lignea Vollenhoven, 1865

(Pl. 6, fig. 9)
Foodplants.–– Capparis (Capparidaceae) (Igarashi & Fukuda, 2000, who illustrate
the early stages as well as the foodplants).
Elodina Felder & Felder, 1865

(pearl whites — Pl. 6, fig. 8)
Range (4+5+6).–– Eastern Java, Lesser Sunda Islands, Sulawesi Region, central
Maluku, New Guinea region, Solomon Islands, New Caledonia, Australia. A genus of
about 16-24 very poorly understood and rather fragile species, mainly occurring in
Australia and the Papuan subregion, with three or four representatives in Sulawesi
(where they appear to be submontane in habitat). According to Klots (1933), Elodina is
“distinct ... with no near relatives.” Probably the genus is an eastern (Papuan) element
in the Sulawesi butterfly fauna, as it occurs in E Java and the Lesser Sunda Islands,
but in the absence of a phylogenetic analysis such an opinion is rather speculative and
only based on the centre of the diversity of the genus.
It seems likely that a still undescribed species occurs in N Sulawesi. Moreover, the
conspecificity of boisduvali and egnatia is disputable.
Foodplants.–– Capparaceae (Capparis).
Key works.–– Common & Waterhouse (1981), Yata (1981a), Parsons (1999).
E. egnatia Godart, 1819

Range (4+5).–– Northern Sulawesi, central Maluku (Ambon, Seram), and Lesser
Sunda Islands (Sumba, Timor and Tanimbar).
Foodplants.–– Capparis (Capparaceae).
–– *E. egnatia boisduvali Fruhstorfer, 1911
*E. sota Eliot, 1956

(Pl. 6, fig. 8)
*E. dispar Röber, 1887

Range (L).–– Kep. Banggai (Banggai, Peleng).
Delias Hübner, 1819

(jezebels — Pl. 6, fig. 10)
Range (W).–– Oriental, south-eastern Palaearctic and Australian Regions, from Sri
Lanka to Solomon Islands, Australia and New Caledonia. This very large genus, with
about 220 species (Yagishita et al., 1993), is widely distributed throughout the Indo-
Australian area but most richly represented in the Papuan Region. Yagishita et al.
(1993) have revised Talbot’s (1928-1937) division of Delias into 20 species groups, to
recognise a total of 22 groups; 7 of these occur in the Sulawesi Region, represented by
10 species (all but one of which are endemic). Of these, five represent three widespre-
ad groupings, but the other five belong to exclusively western groups. Thus, although
the richest potential source-area for Delias on Sulawesi would appear to lie to the east
(in the Papuan Region), the limited taxonomic information available is consistent with
an Asian or Sundanian origin for the local fauna.
Foodplants.–– Anacardiaceae (Mangifera), Buddlejaceae (Buddleja), Dioscoreaceae
(Dioscorea), Fabaceae (Butea, Senna), Loranthaceae (Amyema, Amylotheca, Decaisnina,
Dendrophthoe, Diplatia, Helicanthes, Helixanthera, Korthalsella, Loranthus, Macrosolon,
Muellerina, Notothixos, Oryctanthus, Scurrula, Taxillus), Malvaceae (Abelmoschus), Myr-
taceae (Psidium), Oxalidaceae (Averrhoa), Rubiaceae (Coffea, Nauclea), Rutaceae (Citrus),
Santalaceae (Dendrotrophe, Exocarpos, Santalum), Sterculiaceae (Brachychiton, Pterosper-
mum, Theobroma), Theaceae (Camellia), Viscaceae (Viscum).
Key works.–– Talbot (1928-1937), Yata (1981a), Okano (1989), Yagishita et al.
(1993).
D. kuehni Honrath, 1886

(Kuehn’s Jezebel)
Range (4).–– Sulawesi Region and C Maluku (Buru - see Yagishita et al., 1993; Peg-
gie et al., 1995). A member of the singhapura-group, which includes species occurring
from Burma, Thailand, Malay Peninsula, Sumatra, Borneo and Philippines, to the
Sulawesi Region and Buru.
–– *D. kuehni prinsi Martin, 1912
–– *D. kuehni kuehni Honrath, 1886
Range.–– Kep. Banggai.
–– *D. kuehni sulana Staudinger, 1894
*D. battana Fruhstorfer, 1896

Range (E).–– Sulawesi (C, S). This and the next species, which appear to be closely
related, were included by Talbot (1928-1937) in the widespread nysa-group, with battana
as a subspecies of georgina (a species otherwise distributed through Sundaland, inclu-
ding the Philippines). Yagishita et al. (1993) subdivide the nysa-group into two, to inclu-
de the Sulawesi species in the georgina-group, which is entirely western in distribution.
–– *D. battana battana Fruhstorfer, 1896

–– *D. battana ariae Nakano, 1993
*D. shirozui Yata, 1981

(Shirôzu’s Jezebel)
Range (E).–– Sulawesi (C). Yata (1981b) noted that this species flies at 500-800 m,
whereas in C Sulawesi D. battana is found at 1600-2000 m. Delias kikuoi Okano, 1989,
described from central Sulawesi, is included by Yagishita et al. (1993) as a synonym.
*D. surprisa Martin, 1913

Range (E).–– Sulawesi (C). This species (treated by Talbot as a subspecies of D. bel-
ladonna) is an isolated member of the belladonna-group, otherwise restricted to the
Asian mainland except for belladonna itself, which extends from China to the Malay
Peninsula and Sumatra.
*D. benasu Martin, 1912

(Pl. 6, fig. 10)
Range (E).–– Sulawesi (C). Included by Talbot in the belladonna-group, but placed
by Yagishita et al., 1993, in the (entirely western) pasithoe-group.
–– *D. benasu benasu Martin, 1912
–– *D. benasu subsp. nov. Yamauchi et al. (in press).
Range.–– Sulawesi (C: Mt Tambusisi).
*D. zebuda Hewitson, 1862

Range (R).–– Sulawesi (N, C, S), Salayar, Muna, Kabaena, Kep. Banggai (Peleng)
(Yagishita et al., 1993). Belongs to the widespread belisama group.
*D. melusina Staudinger, 1891

Range (E).–– Sulawesi (N, C). A member of the widespread dorimene-group, Talbot
(1928-1937) considered it to be closely related to D. agostina, which belongs to the
group confined to the Asian mainland (including the Malay Peninsula). The northern
and central populations appear to be distinct races, but Yagishita et al. (1993) do not
differentiate them. The following species is closely related.
*D. kazueae Kitahara, 1986

Range (L).–– Kep. Sula (Taliabu).
*D. rosenbergi Vollenhoven, 1865

(Rosenberg’s Painted Jezebel)
Range (R).–– Sulawesi Region. This species and the next (which should perhaps best
be treated as a single polytypic species) belong to the widespread hyparete-group. Both
are considered by Talbot (1928-1937) as vicariants of hyparete itself, an Indo-Malayan
species distributed from China to the Greater Sunda Islands and the Philippines.
Foodplants.–– Loranthus sp. (Loranthaceae).

–– *D. rosenbergi rosenbergi Vollenhoven, 1865
Range.–– Sulawesi (N, C, SE), Kep. Banggai (Peleng; Nieuwenhuis, 1946).
–– *D. rosenbergi chrysoleuca Mitis, 1893
–– *D. rosenbergi saleyerana Rothschild, 1915
–– *D. rosenbergi munaensis Nakano, 1988
Range.–– Muna, Buton (Yagishita et al., 1993).
*D. mitisi Staudinger, 1894

Range (L).–– Kep. Banggai, Kep. Sula.
–– *D. mitisi banggaiensis Talbot, 1928
–– *D. mitisi mitisi Staudinger, 1894
Range.–– Kep. Sula (Mangole, Sanana, Taliabu: Allyn Museum - see also Yagishita
et al., 1993).
Appias Hübner, 1819

(albatrosses and puffins — Pl. 6, fig. 13)
Range (W).–– Afrotropical, Oriental and Australian Regions. A genus of nearly 40

species divided by Klots (1933) into four subgenera, three of which are represented on
Sulawesi, and by Yata (1981a) into seven groups, including five subgenera, four of
which are found on Sulawesi.
Foodplants.–– Mainly Capparaceae, Euphorbiaceae.
Key works.–– Klots (1933), Corbet & Pendlebury (1992), Common & Waterhouse
(1981), Yata (1981a).
Appias (Appias) Hübner, 1819
Range.–– Oriental Region. Yata (1981a) recognised that lyncida, ithome, nephele,
hombroni and ada collectively form a distinct group, the lyncida-group, but gave no
subgeneric name. Here we propose to include them, tentatively, within the nomino-
typical subgenus. Subgenus Appias includes seven species, three of which occur on
Sulawesi.
A. (A.) lyncida Cramer, 1777

(Chocolate Albatross)
Range (1+2+5+6+7).–– Sri Lanka, southern India, northeastern India, Indo-
China, southern China, Malay Peninsula, Sumatra, Java, Lesser Sunda Islands, Bor-
neo, Palawan, Philippines, Sulawesi Region.
Foodplants.–– Capparis, Crateva, ?Gynotroches (oviposition record in Morrell, 1960)
(Capparaceae). Igarashi & Fukuda (1997) illustrate the early stages.
–– *A. (A.) lyncida gellia Fruhstorfer, 1910
Range.–– Sulawesi (N, C).
–– *A. (A.) lyncida lycaste Felder & Felder, 1865

–– *A. (A.) lyncida subsp. (BMNH)
–– *A. (A.) lyncida subsp. (ZSBS, de Jong in litt.)
Range.–– Salayar, Buton.
–– *A. (A.) lyncida lutatia Fruhstorfer, 1910
Range.–– Kalao, Tanahjampea.
–– *A. (A.) lyncida subsp. (Jurriaanse & Lindemans, 1920)
Range.–– Kabaena.
–– A. (A.) lyncida floresiana Butler, 1898
Range.–– Lesser Sunda Islands (Flores, Alor, ?Sumba), Kep. Tukangbesi (Kaledupa).
*A. (A.) ithome Felder & Felder, 1859

Range (R).–– Sulawesi (N, C, S), Salayar.
Foodplants.–– Capparis (Capparaceae) (Igarashi & Fukuda, 2000, who illustrate the
foodplant and the early stages).
A. (A.) hombroni Lucas, 1852

Range (3).–– Sulawesi Region, N Maluku (Peggie et al., 1995).
–– *A. (A.) hombroni hombroni Lucas, 1852
Range.–– Sulawesi, Kep. Sangihe (Sangihe, Siao).
–– *A. (A.) hombroni tombugensis Fruhstorfer, 1902
Range.–– Sulawesi (C, SE), Kep. Banggai (Peleng).
–– *A. (A.) hombroni sulanorum Fruhstorfer, 1902
Range.–– Kabaena (Jurriaanse & Lindemans, 1920), Kep. Sula (Mangole, Sanana).
Appias (Phrissura) Butler, 1870
Range.–– Malay Peninsula, Sumatra, Borneo, Palawan, Philippines, Sulawesi

Region, ?northern Maluku. According to Corbet (1946a), the subgenus consists of a
single species distributed from the Malay Peninsula to Sulawesi. Yata (1981a), howe-
ver, recognises two allopatric species, the Sulawesi Region populations being conspe-
cific with the Philippine taxon.
A. (P.) aegis Felder & Felder, 1861

(Eastern Forest White)
Range (1+2).–– Philippines (including Palawan), Sulawesi Region, ?northern
Maluku (not confirmed by Peggie et al., 1995).
Foodplants.–– Capparis (Capparaceae - see Nuyda & Kitamura, 1993a).
–– *A. (P.) aegis polisma Hewitson, 1861
–– *A. (P.) aegis aegina Fruhstorfer, 1899
–– *A. (P.) aegis gerasa Fruhstorfer, 1910
Range.–– Kep. Sula (Mangole).
Appias (Hiposcritia) Geyer, 1832
Range.–– Oriental Region. About 13 species, one of which occurs in Sulawesi.
*A (H.) urania Wallace, 1867 (= zondervani Toxopeus, 1950)

Note.–– Formal synonymy of these names will be established by Yata et al. (in
prep.).
Appias (Catophaga) Hübner, 1819
Range.–– Oriental and Australian Regions. Fifteen species, five of which occur in
Key works.–– Yata et al. (in prep.).
A. (C.) nero Fabricius, 1793

(Orange Albatross)
Range (P).–– Burma, Malay Peninsula, Greater Sundas, Bali, Lombok, Palawan,
Philippines, Tanahjampea.
Foodplants.–– Capparis (Capparaceae); Drypetes, Pithecolobium (Euphorbiaceae:
Dupont & Scheepmaker, 1936)
–– A. (C.) nero subsp. (cf. zamobanga C & R Felder, 1862)
Range.–– Kep Talaud (Talaud, Salebabu; BMNH).
–– *A. (C.) nero acuminata Snellen, 1890
A (C.) zarinda Boisduval, 1836

(Eastern Orange Albatross)
Range (4).–– Sulawesi Region, C Maluku (Buru). Formally separated from A. nero
Fabricius by Yata (1981a; see also Peggie et al., 1995).
–– *A (C.) zarinda zarinda Boisduval, 1836
Range.–– Sulawesi, Kabaena, Kep. Tukangbesi, Kep. Banggai (Peleng).
–– *A (C.) zarinda phestus Westwood, 1888
Range.–– Kep. Sangihe, Kep. Talisei.
–– *A (C.) zarinda sulana Fruhstorfer, 1899
*A. (C.) new species Yata & Vane-Wright, in prep.

(= Tachyris nero zarinda ab. aurosa Fruhstorfer, 1899 [unavailable name])
(Golden Albatross – Pl. 6, fig. 13)
Range (E).–– Sulawesi (C, S), Buton.
Note.–– This taxon has previously been treated as a male form of A. zarinda, but
represents a distinct species, as yet only known from the male sex (Yata et al., in prep.).
A. (C.) albina Boisduval, 1836

(White, or Common Albatross)
Range (W).–– Sri Lanka, southern India, Andamans, NE India, Indo-China, SE
China, Hainan, to Malay Peninsula, Sumatra, Java, Lesser Sunda Islands, Borneo,
Palawan, Philippines, Sulawesi Region, Maluku, New Guinea, and northern Aus-
tralia.
Foodplants.–– Capparis, Crataeva (Capparaceae); Drypetes (Euphorbiaceae). Igaras-
hi & Fukuda (2000) illustrate foodplants and early stages.
–– A. (C.) albina albina Boisduval, 1836
Range.–– Borneo, Sulawesi, Tanahjampea, Kep. Banggai (Peleng; Nieuwenhuis,
1946), Kep. Sula, N & C Maluku, eastern Lesser Sunda islands, Aru, Kep. Kai, New
Guinea, northern Australia.
A (C.) paulina Cramer, 1777

(Common Albatross)
Range (W).–– Burma, Indo-China, SE China, Taiwan, Ryukyu Islands, Malay
Peninsula, Nicobars, Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippi-
nes, Sulawesi Region, N & C Maluku, New Guinea, New Caledonia, Vanuatu,
?Samoa, Australia.
Foodplants.–– Capparis (Capparaceae); Drypetes, Putranjiva (Euphorbiaceae). Iga-
rashi & Fukuda (2000) illustrate the early stages.
–– *A (C.) paulina albata Hopffer, 1874 (= urania auctt. nec Wallace, 1867)
Range.–– Sulawesi, Kep. Sula (Mangole).
Note.–– The taxonomy of this subspecies will be clarified by Yata et al.(in prep.).
Saletara Distant, 1885

(albatrosses — Pl. 6, fig. 12)
Range (1+2+3+4+6+7).–– Malay Peninsula, Sumatra, Java, Bali, Borneo, Palawan,

Philippines, Sulawesi Region, N & C Maluku, New Guinea region, Solomon Islands.
Three or four species.
Key works.–– Cowan (1955), Corbet & Pendlebury (1992), Yata (1981a).
S. panda Godart, 1819

(Pl. 6, fig. 12)
Range (1+2+6+7).–– Malay Peninsula, Sumatra, Java, Bali, ?Sumbawa, Borneo,
Palawan, Philippines, Sulawesi Region.
–– *S. panda nigerrima Holland, 1891
Range.–– Sulawesi (N: Allyn Museum; C, S, SE: Roos, 1995).
–– *S. panda watanabei Detani, 1983
–– *S. panda aurantiaca Staudinger, 1894
Cepora Billberg, 1820

(gulls — Pl. 6, fig. 11)
Range (W).–– Oriental, Australian and Pacific Regions. A medium-sized genus of

about 20 species, not less than eight of which have been recorded from the Sulawesi
Region, with five from Sulawesi itself.
Foodplants.–– Capparaceae (Cadaba, Capparis, Maerua), Stachyuraceae (Stachyurus).

Key works.–– Corbet & Pendlebury (1992), Common & Waterhouse (1981), Yata
(1981a).
*C. timnatha Hewitson, 1862

(Pl. 6, fig. 11)
–– *C. timnatha timnatha Hewitson, 1862
–– *C. timnatha filia Fruhstorfer, 1902
–– *C. timnatha subsp. (Roos, 1995)
–– *C. timnatha aurulenta Fruhstorfer, 1899
–– *C. timnatha filiola Fruhstorfer, 1899
–– *C. timnatha soror Fruhstorfer, 1899
*C. celebensis Rothschild, 1892

–– *C. celebensis celebensis Rothschild, 1892
Range.–– Sulawesi (N, C, S), Salayar, Kep. Banggai (Peleng).
–– *C. celebensis kazuyoe Watanabe, 1987
Range.–– Buton.
*C. eurygonia Hopffer, 1874

Range (L).–– Kep. Togian.
Note.–– Separate specific status for this nominal taxon must be open to doubt.
C. perimale Donovan, 1805

(Australian Gull)
Range (P).–– Bawean, Kangean, Lesser Sunda Islands, Salayar, Kep. Tukangbesi,
Muna, C & S Maluku, New Guinea region, Solomon Islands, New Caledonia, Vanu-
atu, Norfolk Island, Fiji, Australia.
–– *C. perimale subsp. (Jurriaanse & Lindemans, 1920)
Range.–– Muna (Galla).
–– *C. perimale toekangbesiensis Jurriaanse & Lindemans, 1920
Range.–– Kep. Tukangbesi (Binongko, Tomea).
–– *C. perimale kuehni Röber, 1885
C. iudith Fabricius, 1787

(Orange Gull)
Range (5+6+7).–– Burma, Thailand, Malay Peninsula, Sumatra, Java, Lesser Sunda
Islands, Borneo, Sulawesi.
–– *C. iudith subsp. (ZSBS; de Jong in litt., Hausmann in litt.)
C. aspasia Stoll, 1790

Range (P).–– Philippines (including Palawan), Kep. Talaud, N & C Maluku, New
Guinea.
Foodplants.–– Capparis (Capparaceae) (Igarashi & Fukuda, 1997).
–– *C. aspasia talautensis Niepelt, 1926
*C. eperia Boisduval, 1836

Range (R).–– Sulawesi, Kep. Banggai (Peleng; Nieuwenhuis, 1946).
*C. fora Fruhstorfer, 1897

–– *C. fora papayatana Watanabe, 1987
–– *C. fora fora Fruhstorfer, 1897
–– *C. fora milos Watanabe, 1987
Range.–– Buton.
*Aoa de Nicéville, 1898

(Pl. 6, fig. 3)
Range (E).–– Sulawesi (monobasic). According to Klots (1933), the relationships of

this distinctive butterfly are uncertain.
*A. affinis Vollenhoven, 1865

(Pl. 6, fig. 3)
Range (E).–– As genus.
Belenois Hübner, 1819

(pioneers — Pl. 6, fig. 7)
Range (4+5+6).–– A genus of about 30 species mainly occurring in the Afrotropical

Region and the Indian subcontinent, discontinuously distributed in the Indo-Austra-
lian region (absent from the Malay Peninsula); the only representative in the Malay
Archipelago and the Australian and Pacific Regions is the highly migratory B. java.
Foodplants.–– Capparaceae.
B. java Sparrman, 1767

(Caper White — Pl. 6, fig. 7)
Range (4+5+6).–– Java, Lesser Sunda Islands, Sulawesi, central Maluku (Ambon),
Bismarck Islands to New Caledonia, Fiji, Samoa, Tonga, Australia.
Foodplant.–– Apophyllum, Capparis (Capparaceae). Igarashi & Fukuda (1997) illu-
strate all life stages.
–– B. java java Sparrman, 1767
Range.–– Java, Lesser Sunda Islands, Sulawesi (N, C, S), Salayar, Tanahjampea,
Maluku (Ambon).
Lycaenidae [Leach], [1815]

(blues, coppers, hairstreaks)
Range.–– Cosmopolitan; about 4000 species; following the standard list of Glo-
BIS (Lamas et al., in prep.) and contrary to Ackery et al. (1999) and a number of ear-
lier authors [e.g., Eliot (1973, 1990) and Kristensen (1976)], the Riodininae are given
family rank. In the GloBIS list, Eliot’s (1990) proposal to include the Lipteninae wit-
hin the Poritiinae, and the Liphyrinae within the Miletinae has been followed,
leaving the Lycaenidae with six subfamilies, five of which are represented in the
Sulawesi Region.
Food.–– A great variety of trophic relationships affect lycaenid butterflies (Fiedler,
1996a); about 150 families of plants recorded as hosts (Fiedler, 1995); one major (Afri-
can) group feeds on minute algae associated with lichens (Henning, 1983; Bampton,
1995); many lycaenids are associated with ants (Pierce et al., 2002), and some are aphy-
tophagous, feeding on the early stages of ants, or various Homoptera tended by them
(Cottrell, 1984; Fiedler, 1991).
Key works.–– Ehrlich (1958), Eliot (1973, 1990), Kristensen (1976), Corbet & Pend-
lebury (1992), Common & Waterhouse (1981), Cottrell (1984), Maschwitz et al. (1984,
1985a, 1985b, 1988), d’Abrera (1986), Bridges (1988b), Shields (1989a), Ackery (1989),
Fiedler (1991, 1995), de Jong et al. (1996), Ackery et al. (1999), Pierce et al. (2002).
Miletinae Reuter, 1896

(moth butterflies, harvesters, brownies, darkies — Pl. 7, figs 2-5)
Range.–– Palaeotropics and Holarctic Region; a small subfamily of about 150

species, divided into five tribes and 18 genera; three tribes and five genera are found
on Sulawesi.
Food.–– Wholly aphytophagous, feeding mainly on Homoptera, sometimes on ant
brood, and often attended by ants.
Key works.–– Eliot (1973), Corbet & Pendlebury (1992), Cottrell (1984), R.L. Kit-
ching (1987), Maschwitz et al. (1985a, 1985b, 1988).
Liphyrini Doherty, 1889

(moth butterflies — not illustrated)
Range.–– A rather small group of about 20 species included in five genera, four of
which are Afrotropical, and represented in the Indo-Australian region by Liphyra.

Food.–– Aphytophagous, feeding wholly on ant brood, ant regurgitations, or
Homoptera (Cottrell, 1984; Fiedler, 1991).
Key works.–– d’Abrera (1977, 1980, 1986).
Liphyra Westwood, 1864

(moth butterflies — not illustrated)
Range (3+6+7).–– Northern India to Thailand, Malay Peninsula, Sumatra, Belitung,

Java, Borneo, Philippines (Luzon, Homonhon: Treadaway, 1995), Sulawesi, N Maluku,
Kep. Kai, New Guinea, Solomons (Samson & Smart, 1980) and Australia. Two species.
Food.–– As subfamily. See also Cottrell (1987) and Fiedler (1991).
Key works.–– d’Abrera (1977, 1986), Samson & Smart (1980), Parsons (1999).
L. brassolis Westwood, 1864

(moth butterfly — not illustrated)
–– L. brassolis robusta Felder & Felder, 1865
Range.–– Sulawesi (N), N Maluku (Halmahera), New Guinea, Manam, Solomon
Islands (Tennent, 2002).
Westwood’s (1888) record of L. brassolis from N Sulawesi stood unconfirmed for
over a century. Samson & Smart (1980) were unable to locate his material, and were
thus uncertain about identity of the Sulawesi population with b. robusta (type-locality:
Halmahera). Ishii (1997) illustrates a single, rather dark male collected near Kotamo-
bagu (Sulawesi Utara), in March 1994, but declined to place it to subspecies; it appears
similar to but not identical with L. b. robusta Felder from Maluku.
Food.–– Brood of Oecophylla ants (Johnson & Valentine, 1986; Cottrell, 1987; Iga-
rashi & Fukuda, 2000).
Miletini Reuter, 1896

(brownies, darkies — Pl. 7, figs 2-4)
Range.–– Palaeotropics; about 80 species in five genera, three of which are found
in the Sulawesi Region.
Food.–– Homoptera (aphids, coccids, membracids) and, more rarely, ant brood;
often attended by ants (e.g. Dolichoderus, Crematogaster, Anoplolepis).
Key works.–– Eliot (1986b).
Allotinus Felder & Felder, 1865

(darkies — Pl. 7, fig. 2)
Range (1+2+5+6+7).–– Northern India to Java, Lesser Sunda Islands, Philippines and
Sulawesi. Three subgenera, two of which occur in Sulawesi. The subgenus not represen-
ted consists of 10 species, distributed from Burma to Sundaland and the Philippines.
Food.–– Aphids, membracids; often ant-attended.
Key works.–– Corbet & Pendlebury (1992), Eliot (1986b).
Allotinus (Allotinus) Felder & Felder, 1865
Range.–– Burma, Malay Peninsula, Sumatra, Java, Borneo, Philippines and Sula-
wesi. A group of seven species divided into two species groups, both represented in
Food.–– Species of this subgenus are recorded to feed on membracids, and be
attended by ants (e.g. Anoplolepis) (R.L. Kitching, 1987; Maschwitz et al., 1988).
A. (A.) fallax Felder & Felder, 1865

Range (P).–– West Malaysia, Sumatra, northern Borneo, Philippines (excluding
Palawan), Kep. Talaud. The only member of the fallax-group to occur in the Sulawesi
Region.
–– A. (A.) fallax aphacus Fruhstorfer, 1913
Range.–– Southern Philippines, Kep. Talaud (one female: Cassidy, 1995a).
*A. (A.) major Felder & Felder, 1865

Range (R).–– Sulawesi, Kep. Sangihe, Kep. Banggai (Peleng), Kep. Sula (Mangole).
This and the next species comprise the major-group, which is thus restricted to the
Sulawesi Region.
Food.–– Terentius (Membracidae); attended by Anoplolepis (Formicidae) (R.L. Kit-
ching, 1987). Igarashi & Fukuda (2000) illustrate larva and pupa.
*A. (A.) maximus Staudinger, 1888

Range (E).–– Sulawesi (N, C, S: Cassidy, 1995a).
Allotinus (Paragerydus) Distant, 1884

(Pl. 7, fig. 2)
Range.–– Northern India, Burma, Malay Peninsula, Sumatra, Java, Borneo, Lesser
Sunda Islands, Philippines and Sulawesi Region. Of the 16 species included, four
occur on Sulawesi.
Food.–– A species of this subgenus has been recorded to feed on Pseudoregma
(Hormaphididae), attended by Crematogaster; in another case, the first instar larvae
probably fed on coccids, and thereafter on brood of a myrmicine ant, Myrmicaria
(Maschwitz et al., 1988), or in association with Anoplolepis (Fiedler, 1996b).
A. (P.) samarensis Eliot, 1986

Range (2).–– Philippines (Samar, Leyte, Mindanao: Treadaway, 1995), Sulawesi.
–– *A. (P.) samarensis russelli Eliot, 1986
*A. (P.) macassarensis Holland, 1891

–– *A. (P.) macassarensis macassarensis Holland, 1891
Range.–– Sulawesi (C, S), Kep. Banggai.
–– *A. (P.) macassarensis menadensis Eliot, 1967
Range.–– Sulawesi (N), Bangka.
A. (P.) albatus Felder & Felder, 1865

(Pl. 7, fig. 2)
Range (2).–– Philippines (Luzon, Marinduque, Samar: Treadaway, 1995), Sulawesi.
–– *A. (P.) albatus albatus Felder & Felder, 1865
Range.–– Sulawesi (N: Cassidy, 1995a).
A. (P.) unicolor Felder & Felder, 1865

(Lesser Darkie)
Range (2+5+6+7).–– Assam, Indo-China, Malay Peninsula, Sumatra, Java, Lesser
Sunda Islands, Borneo, Philippines (Bohol, Mindoro, Sanga Sanga, Tawitawi: Treada-
way, 1995), Sulawesi Region.
Food.–– Oviposition recorded on 5 aphid species, 1 psyllid and 2 membracids;
associated with ants (Anoplolepis, Formicinae) (Fiedler & Maschwitz, 1989).
–– *A. (P.) unicolor zitema Fruhstorfer, 1916
Range.–– Sulawesi, Kep. Banggai, Kep. Sula (Mangole).
Logania Distant, 1884

(mottles — Pl. 7, fig. 3)
Range (W).–– Oriental Region eastwards to New Guinea and Bismarcks, including
Lesser Sunda Islands. Eleven species, three of which are Sulawesi Region endemics.
Food.–– Homoptera (e.g. Pseudoregma, coccids, membracids, aphids) and, in some
cases, their secretions (or possibly even ant larvae: Parsons, 1999); attended by ants
(e.g. myrmicines Leptothorax, Rhoptromyrmex, Technomyrmex and the dolichoderine
Hypoclinea), apparently in some cases (at least) in permanent specific associations invol-
ving the pupae as well as larvae (Maschwitz et al., 1988; Fiedler, 1993; Parsons, 1999).
Key works.–– Corbet & Pendlebury (1992), Eliot (1986b).
*L. paluana Eliot, 1986

*L. obscura Röber, 1886

(Pl. 7, fig. 3)
Range (R).–– Sulawesi (?N, S), Buton, Kep. Tukangbesi, Kep. Banggai.
*L. dumoga Cassidy, 1995

The species bears a superficial resemblance to L. marmorata palawana. The record of
the latter species from Sulawesi by Seki et al. (1991) is probably based on confusion
with the present taxon.
Miletus Hübner, 1819

(brownies — Pl. 7, fig. 4)
Range (W).–– Oriental Region, Wallacea and New Guinea (Eliot, 1986b; no Miletus
from New Guinea noted by Parsons, 1999). The genus includes about 25 species divi-
ded into five species-groups; the four species found on Sulawesi represent two of
these groups.
Food.–– Aphids and coccids; often ant-attended (e.g., Maschwitz et al., 1985a, 1988,
record a Malayan Miletus on coccids and on hormaphids, including Pseudoregma, in all
cases attended by Dolichoderus; Fiedler, 1996b, notes association with Hypoclinea).
Key works.–– Eliot (1961, 1986b), Corbet & Pendlebury (1992).
M. boisduvali Moore, 1858

(Boisduval’s Brownie)
Range (3+4+5+6+7).–– Sumatra, Java, Lesser Sunda Islands, Borneo, Sulawesi
Region, N & C Maluku, New Guinea. This is the Sulawesi representative of the boisdu-
vali-group, which includes three other species.
Food.–– Ceratophis (Aphididae), Pseudococcus (Coccidae); attended by Dolichoderus
(Formicidae).
–– *M. boisduvali diotrophes Fruhstorfer, 1913
Range.–– Sulawesi (E).
–– M. boisduvali boisduvali Moore, 1858
Range.–– As species, including Kep. Sula (Mangole, Sanana), but excluding Sula-
wesi, Timor and Kai Islands.
*M. celinus Eliot, 1961

Range (E).–– Sulawesi (S). This and the remaining two Sulawesi Miletus belong to
the symethus-group, which includes a total of about eight species.
*M. rosei Cassidy, 1995

M. leos Guérin-Ménéville, 1830

(Pl. 7, fig. 4)
Range (3+4+5).–– Lesser Sunda Islands, Sulawesi Region, N & C Maluku, New
Guinea.
–– *M. leos maximus Holland, 1890
Range.–– Sulawesi (N, C, S, SE), Kep. Sangihe, Kep. Talaud, Buton, Muna, Kep.
Banggai (Peleng) (see Cassidy, 1995a).
–– *M. leos catoleucos Fruhstorfer, 1913
Range.–– Salayar, Kep. Tukangbesi.
–– *M. leos tellus Fruhstorfer, 1913
Range.–– “Java” (doubtful), “Wetar” (doubtful), ?Sumbawa (Eliot, 1961), Tanah-
jampea.
–– *M. leos subsp. (Eliot, 1961)
Range.–– Kep. Tukangbesi.
–– *M. leos mangolicus Fruhstorfer, 1913
Spalgini Toxopeus, 1929

(apeflies, or harvesters — Pl. 7, fig. 5)
Range.–– As subfamily; two genera, one being the monotypic Nearctic genus
Feniseca.
Note.–– Some authors have suggested that the Spalgini are more closely related to
the Polyommatinae than to the true Miletinae.
Food.–– Homoptera (Coccidae, Pemphigidae, Pseudococcidae); not associated
with ants.
Key works.–– Eliot (1973), Corbet & Pendlebury (1992), Cottrell (1984).
Spalgis Moore, 1879

(apeflies — Pl. 7, fig. 5)
Range (W).–– Palaeotropics. A small genus of about 10 species (only 5 according to

Parsons, 1999), only one of which occurs on Sulawesi.
Food.–– Coccids and pseudococcids, often camouflaging themselves with the
debris of their prey (Parsons, 1999).
Key works.–– Corbet & Pendlebury (1992), Cottrell (1984), Parsons (1986).
S. epius Westwood, 1851

(Apefly — Pl. 7, fig. 5)
Range (W).–– Sri Lanka, India, Malay Peninsula, Sumatra, Java, Lesser Sunda
Islands, Borneo, Palawan, Philippines (Treadaway, 1995), Sulawesi Region, N & C
Maluku, Kep. Kai.
Food.–– Dactylopius (Coccidae). Igarashi & Fukuda (2000) illustrate the early stages.
–– *S. epius substrigatus Snellen, 1878
–– *S. epius subsp. (BMNH)
Poritiinae Doherty, 1886

(gems and bluejohns; zulus, Acraea mimics — Pl. 7, fig. 1)
Range.–– Afrotropical and Oriental Regions; about 600 species divided amongst
three tribes, Pentilini, Liptenini and Poritiini. The former two are Afrotropical and
contain, with about 122 and 400 species, respectively, by far the larger part of the
subfamily.
Foodplants.–– Lichens and microscopic algae; Fagaceae.
Key works.–– Eliot (1973), Corbet & Pendlebury (1992), d’Abrera (1986).
Poritiini Doherty, 1886
Range.–– Oriental Region, including Philippines and Sulawesi; a small tribe of

about 65, mostly rare species included within five genera; two of these genera are now
known to be represented on Sulawesi. According to Osada (1994), more Poritiinae
from Sulawesi await description.
Foodplants.–– Fagaceae.
Key works.–– Eliot (1973), Corbet & Pendlebury (1992), d’Abrera (1986).
Poritia Moore, 1866

(gems — not illustrated)
Range (1+2+6+7).–– North-eastern India, Malay Peninsula, Sumatra, Java, Borneo,

Palawan, Philippines, Sulawesi.
Foodplants.–– Fagaceae (Castanea; P. sumatrae in Sabah also on Lithocarpus, pers.
obs. by K. Fiedler). Larvae gregarious (processionary), not attended by ants.
Over 20 species, with two recently described representatives from Sulawesi.
Key works.–– Eliot (1957), Corbet & Pendlebury (1992), Osada (1987, 1994).
*P. palos Osada, 1987

*P. personata Osada, 1994

Deramas Distant, 1886

(gems and bluejohns — Pl. 7, fig. 1)
Range (2+6+7).–– Burma, Malay Peninsula, Sumatra, Java, Borneo, Philippines

(excluding Palawan), Sulawesi. About 30 species, of which four endemics occur in
Central Sulawesi.
Key works.–– Eliot (1964b, 1970), D’Abrera (1986), Osada (1987, 1994), Corbet &
Pendlebury (1992).
*D. nigrescens Eliot, 1964

(Pl. 7, fig. 1)
Range (E).–– Sulawesi. Osada (1994) records this species from Palolo, near Palu.
*D. suwartinae Osada, 1987

*D. nanae Osada, 1994

*D. masae Kawai (in Osada), 1994

Curetinae Distant, 1884

(sunbeams — Pl. 7, fig. 6)
Range.–– Oriental Region, including Lesser Sunda Islands, just extending into
Palaearctic and Papuan Regions; 18 species in 3 species groups in a single genus.
Foodplants.–– Fabaceae (Abrus, Adenanthera, Millettia, Pongamia), Meliaceae; someti-

mes associated with ants (e.g. Anoplolepis, Formicinae: DeVries, 1984; but perhaps not
normally: Fiedler et al., 1995, Fiedler, 1996b).
Key works.–– Shirôzu & Yamamoto (1957), Eliot (1973, 1990), DeVries et al. (1986),
Fiedler et al. (1995).
Curetis Hübner, 1819

(sunbeams — Pl. 7, fig. 6)
Range (W).–– As subfamily. Two species occur on Sulawesi, both belonging to the
thetis-group.
Foodplants.–– As subfamily.
Key works.–– Evans (1954), d’Abrera (1986), Eliot (1990), Corbet & Pendlebury
(1992).
*C. venata Fruhstorfer, 1908

–– *C. venata venata Fruhstorfer, 1908
–– *C. venata saleyerensis Chapman, 1915
C. tagalica Felder & Felder, 1862

(Pl. 7, fig. 6)
Range (1+2+6+7).–– South Vietnam, Malay Peninsula, Sumatra, Java, Bali, Borneo,
Palawan, Philippines, Sulawesi Region.
Foodplant.–– Millettia atropurpurea (Fabaceae) (unpubl. record by Peter Seufert
from Ulu Gombak, West Malaysia). Larvae not attended by ants.
–– *C. tagalica celebensis Felder & Felder, 1865
–– *C. tagalica talautensis Chapman, 1915
–– *C. tagalica brunnescens Ribbe, 1926 (= thetis nakamotoi Detani, 1983)
Range.–– Kep. Banggai (Peleng), Kep. Sula (Mangole).
Theclinae Swainson, 1830

(hairstreaks — Pl. 7, figs 7-25)
Range.–– Cosmopolitan; one of the largest subfamilies within the Rhopalocera,

with well over 2000 species in 19 tribes and numerous genera. It is very well represen-
ted in South East Asia; 12 of the tribes occur on Sulawesi.
Foodplants.–– A very wide range of plant families, including: Araliaceae, Arecace-
ae, Asteraceae, Barringtoniaceae, Casuarinaceae, Celastraceae, Combretaceae, Convol-
vulaceae, Dioscoreaceae, Ebenaceae, Ehretaceae, Elaeagnaceae, Elaeocarpaceae, Epa-
cridaceae, Euphorbiaceae, Fabaceae, Fagaceae, Flagellariaceae, Hippocastanaceae,
Lauraceae, Lecythidaceae, Loranthaceae, Lythraceae, Malpighiaceae, Malvaceae,
Melastomataceae, Moraceae, Myrsinaceae, Myrtaceae, Olacaceae, Orchidaceae, Oxali-

daceae, Pittosporaceae, Polypodiaceae, Proteaceae, Punicaceae, Rhamnaceae, Rhizop-
horaceae, Rosaceae, Rubiaceae, Rutaceae, Santalaceae, Sapindaceae, Saxifragaceae,
Smilacaceae, Sterculiaceae, Theaceae, Urticaceae, Verbenaceae. Some Theclinae are
associated with ants, including some that feed on ant brood (Fiedler, 1991).
Key works.–– Eliot (1973), d’Abrera (1977, 1986), Corbet & Pendlebury (1992).
Luciini Waterhouse & Lyell, 1914

(jewels)
Range.–– Australian Region, with minor representation in South East Asia; in

total, about 150 species in six or seven genera. A single undescribed species is known
from Sulawesi.
Foodplants.–– Over 30 families of flowering plants (Fiedler, 1991); associated with
ants.
Key works.–– Eliot (1973), d’Abrera (1977), Common & Waterhouse (1981).
Hypochrysops Felder & Felder, 1860

(jewels — not illustrated)
Range (3+4+7).–– A large genus of about 60 species, confined to the Australian

and Papuan Regions, including Maluku, except for a single species (H. coelisparsus
Butler) in the Oriental Region (southern Thailand, Malay Peninsula, Kep. Riau,
?Sumatra, Mentawi Islands, Borneo, ?Sulawesi - Parsons, 1999), and an undescribed
species reported from Sulawesi.
Foodplants.–– Araliaceae, Asteraceae, Barringtoniaceae, Casuarinaceae, Combre-
taceae, Dioscoreaceae, Elaeocarpaceae, Epacridaceae, Euphorbiaceae, Fabaceae, Lecyt-
hidaceae, Loranthaceae, Malpighiaceae, Melastomataceae, Myrsinaceae, Myrtaceae,
Polypodiaceae, Proteaceae, Pteridophyta, Rhamnaceae, Rhizophoraceae, Rosaceae,
Rubiaceae, Santalaceae, Sapindaceae, Smilacaceae, Sterculiaceae, Theaceae, Verbe-
naceae; attended by ants (Crematogaster, Iridomyrmex, Pheidole).
Key works.–– Common & Waterhouse (1981), Sands (1986), d’Abrera (1990).
*H. species (Sands, 1986; in collection of E. Tsukada)

Range (E).–– Sulawesi (C). According to Sands (1986) this species, collected at Palo-
po in 1978, belongs to the H. chrysanthis-group (a group comprising only three other
species: the western coelisparsus (noted by Parsons, 1999, as occurring on Sulawesi, but
unconfirmed here), H. apollo Miskin from Queensland and New Guinea, and chrysanthis
Felder from central Maluku), and is probably most closely related to chrysanthis itself.
Arhopalini Bingham,1907
(oakblues — Pl. 7, figs 7-9)
Range.–– Oriental and Australian Regions, with slight extension into Palaearctic;
about 250 species in six genera, the great majority of which belong to Arhopala s.l. Four
of the genera are represented in the Sulawesi Region.
Foodplants.–– Anacardiaceae, Barringtoniaceae, Boraginaceae, Chrysobalanaceae,

Clusiaceae, Combretaceae, Ehretiaceae, Euphorbiaceae, Fabaceae, Fagaceae, Laurace-
ae, Loranthaceae, Lythraceae, Malvaceae, Meliaceae, Myrtaceae, Sapindaceae, Stercu-
liaceae, Verbenaceae. Attended by ants.
Key works.–– Eliot (1973), Corbet & Pendlebury (1992).
Arhopala Boisduval, 1832

(oakblues — Pl. 7, fig. 7)
Range (W).–– Oriental and Australian Regions, extending to Australia, the Solo-
mon Islands and Japan. About 200 species, with at least 12 occurring on Sulawesi (in
contrast, Seki et al., 1991, list some 90 species from Borneo).
Foodplants.–– Most species on Fagaceae or Euphorbiaceae, but using a wide range
of other plant families as well. The Fabaceae are positively recorded for only two spe-
cies, A. pseudocentaurus and A. similis (Peter Seufert unpublished; Megens, 2002). All
species appear to be attended by ants, either facultatively or in an obligate relations-
hip (the latter with e.g. Oecophylla, Crematogaster: Maschwitz et al., 1984; Fiedler &
Seufert, 1995; Fiedler, 1996b). One Australian species (A. wildei) is myrmecophagous
inside Polyrhachis nests.
Key works.–– Corbet (1941, 1946b), Evans (1957a), Eliot (1963, 1972), Corbet &
Pendlebury (1992), Seki et al. (1991), Megens (2002).
A. eridanus Felder, 1860

(Pl. 7, fig. 7)
Range (1+3+4).–– Philippines (Balabac, Cuyo, Palawan), Sulawesi Region, N & C
Maluku.
–– *A. eridanus lewara Ribbe, 1926
Range.–– Sulawesi, Kep. Banggai (Peleng: Hayashi, 1984).
–– *A. eridanus elfeta Hewitson, 1869
A. annulata Felder, 1860

Range (1+2+4).–– Palawan, Philippines (Mindanao: Treadaway, 1995), Sulawesi
(C), Kep. Banggai, central Maluku (Buru, Ambon).
*A. dohertyi Bethune-Baker, 1903

(Doherty’s Oakblue)
*A. irregularis Bethune-Baker, 1903

Range (R).–– Sulawesi, Kep. Banggai (Peleng).
*A. argentea Staudinger, 1888

*A. sangira Bethune-Baker, 1897

Range (L).–– Kep. Sangihe.
*A. hercules Hewitson, 1862

Range (E).–– Sulawesi, ?northern Maluku (including Obi), ?New Guinea region
(non-Sulawesi populations apparently excluded as separate species by Parsons, 1999).
*A. quercoides Röber, 1886

A. cleander Felder, 1860

Range (2+4+5+6+7).–– Burma, Malay Peninsula, Sumatra, Java, Lombok, Borneo,
Philippines (Luzon, Camiguin de Luzon, Mindanao, Leyte, Negros, Sibutu: Treada-
way, 1995), Sulawesi Region, central Maluku (including Buru), New Guinea region.
–– *A. cleander sostrata Fruhstorfer, 1914
Range.–– Sulawesi (S), Salayar, Kep. Banggai.
A. phaenops Felder & Felder, 1865

Range (P).–– Malay Peninsula, Sumatra, Java, Borneo, Palawan, Philippines (inclu-
ding Luzon and Mindanao: Treadaway, 1995), Kep. Sangihe, Kep. Talaud, Kep. Bang-
gai, Maluku.
–– *A. phaenops phaenops Felder, 1865
Range.–– ?Philippines, Kep. Sangihe, Kep. Talaud, Kep. Banggai (Peleng - Seki et
al., 1991), northern Maluku.
A. alitaeus Hewitson, 1862

Range (1+2+6+7).–– Burma, Malay Peninsula, Sumatra, Java, Borneo, Palawan,
Philippines (including Luzon and Mindanao: Treadaway, 1995), Sulawesi Region.
–– *A. alitaeus alitaeus Hewitson, 1862
Range.–– Sulawesi, Kep. Banggai.
*A. acetes Hewitson, 1862

Range (R).–– Sulawesi, Kep. Talaud, Kep. Tukangbesi, Kep. Banggai.
A. tephlis Hewitson, 1869

Range (3).–– Sulawesi, northern Maluku.
–– *A. tephlis bicolora Röber, 1886
A. araxes Felder & Felder, 1865

Range (5+6).–– Sumatra, Java, Lesser Sunda Islands, Sulawesi Region (records
from New Guinea region not confirmed by Tennent, 2002, or Parsons, 1999; not
known from Maluku).
–– *A. araxes araxes Felder & Felder, 1865
Range.–– Sulawesi, Kep. Sangihe, ?Kep. Banggai, Kep. Sula (Mangole).
–– *A. araxes talauta Evans, 1957
–– *A. araxes verelius Fruhstorfer, 1914

Range.–– Kalao.
A. philander Felder & Felder, 1865

Range (P).–– Kep. Sangihe, Maluku, New Guinea region.
–– A. philander philander Felder & Felder, 1865
Range.–– Kep. Sangihe, N Maluku.
*A. straatmani Nieuwenhuis, 1969

(Straatman’s Oakblue)
A. species (Detani, 1983, as pseudocentaurus Doubleday, 1847)

Detani (1983) recorded an Arhopala from Kep. Banggai (Peleng) as an unnamed
subspecies of A. pseudocentaurus. According to Harish Gaonkar (pers comm.), there
has been a long-standing confusion over the identity of A. centaurus Fabricius, 1775, of
which it now appears that pseudocentaurus is a strict synonym. Gaonkar has establish-
ed that the original material of centaurus came from Java, not Malaya (Evans, 1957a) or
Australia (e.g. Braby, 2000). Seki et al. (1991) do not list pseudocentaurus or centaurus
from the Sulawesi Region. Without access to material, the identity of this Arhopala can
only be guessed at.
Range (P).–– Kep. Banggai (Peleng); probable wider range uncertain.
Flos Doherty, 1889

(plushblues — Pl. 7, fig. 8)
Range (1+2+5+6+7).–– Indo-China, Malay Peninsula, Sumatra, Java, Lesser Sunda

Islands, Borneo, Philippines and Sulawesi Region. About 10 species, four of which
have been recorded from Sulawesi.
Foodplants.–– Fagaceae, Lythraceae, Myrtaceae. Larvae always attended by ants
(Dolichoderus spp.), probably an obligate relationship, as indicated by observations on
Bornean F. anniella (pers. obs. K. Fiedler).
Key works.–– Evans (1957a), Corbet & Pendlebury (1992).
F. diardi Hewitson, 1862

(Shining Plushblue)
Range (1+2+6+7).–– Northern India, Malay Peninsula, Sumatra, Java, Borneo,
Palawan, Philippines (including Luzon, Mindanao and Tawitawi: Treadaway, 1995),
Sulawesi.
Foodplant.–– Lithocarpus (Fagaceae) (Corbet & Pendlebury, 1992).
Note.–– Seki et al. (1991) do not list diardi for Sulawesi, so the specific assignment
of imperiosa is perhaps questionable.
–– *F. diardi imperiosa Fruhstorfer, 1914
*F. kuehni Röber, 1887

(Kuehn’s Plushblue)
Range (R).–– Sulawesi, Kep. Banggai.
*F. arca de Nicéville, 1893

F. apidanus Cramer, 1777

(Plain Plushblue — Pl. 7, fig. 8)
Range (P).–– Assam, Malay Peninsula, Sumatra, Java, Lesser Sunda Islands, Bor-
neo, Palawan, Philippines, Sulawesi Region.
Foodplants.–– Lagerstroemia (Lythraceae); Eugenia, Syzygium (Myrtaceae).
–– F. apidanus palawanus Staudinger, 1889
Range.–– Palawan, Balabac, Philippines (Luzon, Mindoro, Panay, Samar, Bohol,
but not Mindanao - see Treadaway, 1995), ?Sulawesi.
Note.–– Seki et al. (1991) include apidanus from Sulawesi without raising doubts,
but this may refer to the next subspecies; the presence of this Philippine race on
Sulawesi requires confirmation; Treadaway lists F. apidanus himna Fruhstorfer, 1914,
from Mindanao.
–– F. apidanus apidanus Cramer, 1779
Range.–– Java to Sumbawa, Tanahjampea.
Semanga Distant, 1884

(rededges — not illustrated)
Range (P).–– Malay Peninsula, Sumatra, Java, Borneo, Sanga Sanga (Treadaway,
1995), Kep. Banggai. Two very rare species, discontinuously distributed, one being
endemic to Banggai; the genus has not been recorded from Sulawesi.
Foodplants.–– Including Fabaceae (Saraca); constantly attended by Dolichoderus
ants (Fiedler & Seufert, 1995; Seufert & Fiedler, 1996b).
Key works.–– Corbet & Pendlebury (1992), d’Abrera (1986).
*S. helena Röber, 1887

(Helena Rededge)
Range (L).–– Kep. Banggai.
Surendra Moore, 1879

(acacia blues — Pl. 7, fig. 9)
Range (1+2+6+7).–– Sri Lanka, India, China, Indo-China, Malay Peninsula, Sumatra,
Java, Bali, Borneo, Palawan, Philippines, Sulawesi. A small genus of about three to five
species, represented by a single species in Sulawesi, at the eastern limit of the range.
Note.–– Takanami (1989) appears to regard S. v. samina as a separate Sulawesi
endemic, but we prefer here to follow Cantlie (1962) in recognising only three species
within the genus; further work is evidently required.
Foodplants.–– Fabaceae (Acacia, Albizia, Paraserianthes); facultatively attended by
various ants.
Key works.–– Cantlie (1962, 1964), d’Abrera (1986), Takanami (1989), Fiedler (1992b).
S. vivarna Horsfield, 1829

(Acacia Blue — Pl. 7, fig. 9)
Range (1+6+7).–– As genus, except not recorded from China, or on Philippines
proper (where it is replaced by S. manilana Felder & Felder: see Treadaway, 1995, who
records S. vivarna from Balabac, Palawan and Calamian group only). See also note
above (under genus) regarding status of subspecies samina.
Larvae facultatively attended by ants (e.g. Anoplolepis: Maschwitz et al. 1985b)
–– *S. vivarna samina Fruhstorfer, 1904
Note.–– Igarashi & Fukuda (2000) list this taxon as a separate species.
Foodplants.–– Acacia (Fabaceae).
Range.–– Sulawesi, ?Kep. Banggai.
Amblypodiini Doherty, 1886

(leaf, fig-tree and silverstreak blues — Pl. 7, figs 10, 11)
Range.–– Palaeotropics; a small tribe of three genera, two of which occur in the
Oriental Region; both are known from Sulawesi.
Foodplants.–– Celastraceae, Dipterocarpaceae, Moraceae, Olacaceae, Rubiaceae.
Amblypodia Horsfield, 1829

(leaf blues — Pl. 7, fig. 10)
Range (W).–– Oriental and Australian Regions, east to the Solomon Islands (Ten-
nent, 2002), but not Australia. A genus of about 15 species, with a single representati-
ve in Sulawesi.
Foodplants.–– Olacaceae. Ant-associations not positively recorded.
Key works.–– d’Abrera (1977, 1986), Corbet & Pendlebury (1992).
A. narada Horsfield, 1829

(Blue Leaf Blue — Pl. 7, fig. 10)
Range (1+2+3+6+7).–– Burma, Malay Peninsula, Sumatra, Java, Borneo, Palawan,
Philippines, Sulawesi, northern Maluku.
Foodplants.–– Olax (Olacaceae).
–– *A. narada confusa Riley, 1922
Iraota Moore, 1881

(silverstreak blues — Pl. 7, fig. 11)
Range (1+2+5+6+7).–– Oriental Region, including Lesser Sunda Islands (Takana-

mi, 1986a), Philippines and Sulawesi Region. A small genus of about four species,
with a single member represented on Sulawesi.
Foodplants.–– Moraceae.
Key works.–– Corbet & Pendlebury (1992), Takanami (1985), d’Abrera (1986), Seki
et al. (1991).
I. rochana Horsfield, 1829

(Scarce Silverstreak Blue — Pl. 7, fig. 11)
Range (1+2+6+7).–– Assam, Malay Peninsula, Sumatra, Java, Bali, Borneo, Pala-
wan, Philippines, Sulawesi Region.
Foodplants.–– Ficus (Moraceae).
–– *I. rochana johnsoniana Holland, 1890
–– *I. rochana mangolina Fruhstorfer, 1911
Hypotheclini Eliot, 1973

(Pl. 7, fig. 12)
Range.–– Papuan Region and Wallacea (Philippines and Sulawesi). A small group
of two genera, one of which occurs in Sulawesi.
Key works.–– Eliot (1973).
Hypothecla Semper, 1890

(Pl. 7, fig. 12)
Range (1+2).–– Palawan, Philippines (Treadaway, 1995) and Sulawesi Region.

Two rare species.
Key works.–– d’Abrera (1986).
*H. honos de Nicéville, 1898

(Pl. 7, fig. 12)
Range (R).–– Sulawesi, Kep. Banggai (Peleng; Nieuwenhuis, 1946).
Loxurini Swinhoe, 1910

(imperials, yamflies — Pl. 7, fig. 13)
Range.–– Oriental Region and Wallacea. Six genera, only one of which is found
in Sulawesi. According to Eliot (in Corbet & Pendlebury, 1978), this and the next
two tribes are closely related and should perhaps be combined.
Foodplants.–– Dioscoreaceae, Smilacaceae, Solanaceae; some species attended by
ants (Fiedler, 1994a).
Loxura Horsfield, 1829

(yamflies — Pl. 7, fig. 13)
Range (1+2+5+6+7).–– Sri Lanka to Sundaland, Palawan, Philippines, Lesser Sunda

Islands and southern Sulawesi Region. Two species, the more widespread of which
occurs on Sulawesi.
Key works.–– d’Abrera (1986).
L. atymnus Stoll, 1780

(Yamfly — Pl. 7, fig. 13)
Range (5+6+7).–– Sri Lanka, India, Malay Peninsula, Sumatra, Java, Lesser Sunda
Islands, Borneo, Philippines (Luzon: Treadaway, 1995), Sulawesi Region.
Foodplants.–– Dioscorea (Dioscoreaceae); Smilax (Smilacaceae); Solanum (Solanace-
ae). Igarashi & Fukuda (2000) illustrate all life stages.
–– *L. atymnus sulawesiensis Takanami, 1986
–– *L. atymnus subsp. (BMNH)
–– *L. atymnus subsp. (BMNH)
Range.–– Kalao.
Horagini Swinhoe, 1910

(Pl. 7, fig. 14)
Range.–– Oriental Region, from Sri Lanka to Taiwan and eastwards to New Gui-
nea. Two genera, only one of which occurs in Sulawesi; the other, which is monobasic,
is restricted to the Indian subregion.
Foodplants.–– Bombacaceae, Coriariaceae, Euphorbiaceae, Lauraceae, Loranthace-
ae, Myrtacae, Rubiaceae, Sapindaceae, Styracaceae.
Key works.–– Cowan (1966b), Eliot (1973), Corbet & Pendlebury (1992).
Horaga Moore, 1881

(onyxes — Pl. 7, fig. 14)
Range (W).–– As tribe, including the Philippines, Maluku and Lesser Sunda
Islands. About ten species, four of which are found on Sulawesi.
Foodplants.–– Bombacaceae (Kuroko & Lewvanich, 1993), Coriariaceae, Euphor-
biaceae (Fiedler, 1991; Igarashi & Fukuda, 2000), Lauraceae (Bascombe et al., 1999).
Ant-associations so far unknown.
Key works.–– Cowan (1966b), Corbet & Pendlebury (1992), Eliot (1986a), d’Abrera
(1986), Seki et al. (1991), Schroeder et al. (2001).
H. syrinx Felder, 1860

(Yellow Onyx)
Range (W).–– Northern India, Malay Peninsula, Sumatra, Java, Bali, Lombok (Par-
sons, 1999), Borneo, Palawan, Philippines (Treadaway, 1995; Schroeder et al., 2001),
Sulawesi, N & C Maluku, New Guinea (Parsons, 1999).
–– *H. syrinx permagna, Fruhstorfer, 1912
*H. selina Grose Smith, 1895

(Pl. 7, fig. 14)
Range (E).–– Sulawesi (C, S).
H. chalcedonyx Fruhstorfer, 1914

Range (2+6+7).–– Singapore, Bali, Borneo, Philippines (Luzon, Marinduque, Negros:
Treadaway, 1995; Sibutu, Mindoro, Mindanao: Schroeder et al., 2001), Sulawesi.
–– *H. chalcedonyx taweya Cowan, 1966
*H. sohmai Osada, 2001

Range (E).–– Sulawesi (C, S; Osada, 2001).
Cheritrini Swinhoe, 1910

(imperials, posies — Pl. 7, fig. 15)
Range.–– Afrotropical and Oriental Regions. Of the four Oriental genera, only one
is represented on Sulawesi.
Foodplants.–– ?Annonaceae (oviposition only), Barringtoniaceae, Clusiaceae, Dip-
terocarpaceae, Fabaceae, Lauraceae, Lecythidaceae, Meliaceae, Myrtaceae, Rubiaceae,
Sapindaceae.
Key works.–– Cowan (1967), Eliot (1973), Corbet & Pendlebury (1992).
Drupadia Moore, 1884

(posies — Pl. 7, fig. 15)
Range (1+2+6+7).–– India to Java, Philippines and Sulawesi. About 15 species, one
of which occurs in Sulawesi.
Foodplants.–– As tribe; attended by ants (e.g. Crematogaster, Pheidole), either in
facultative or obligate relationship (Fiedler, 1996b).
Key works.–– Cowan (1974), Corbet & Pendlebury (1992), d’Abrera (1986), Seki et
al. (1991).
D. theda Felder & Felder, 1862

(Dark Posy — Pl. 7, fig. 15)
Range (1+2+7).–– Burma, Malay Peninsula, Sumatra, Borneo, Palawan, Philippi-
nes, Sulawesi Region.
Foodplants.–– ?Annonaceae (oviposition only); Barringtonia (Barringtoniaceae);
Saraca, Bauhinia, Millettia (Fabaceae); Garcinia (Clusiaceae); Lansium (Meliaceae); Ixora
(Rubiaceae); Arytera, Pometia, Lepisanthes (Sapindaceae), always at young growth or
inflorescences (Seufert & Fiedler, 1996a; Igarashi & Fukuda, 2000). Obligate associa-
tion with Crematogaster ants (Maschwitz et al., 1985a; Seufert & Fiedler, 1996a,b). Iga-
–– *D. theda thaliarchus Staudinger, 1888
–– *D. theda inexpectata Ribbe, 1926
–– *D. theda namusa Hewitson, 1863

–– *D. theda bangkaiensis Ribbe, 1926
Aphnaeini Distant, 1884

(silverlines — not illustrated)
Range.–– Afrotropical, Oriental and Palaearctic Regions. This large group of spe-
cies, divided into about 16-18 genera, is primarily Afrotropical; represented in the
Oriental Region by a few species of Spindasis.
Foodplants.–– Anacardiaceae, Asteraceae, Bruniaceae, Capparaceae, Cistaceae,
Combretaceae, Convolvulaceae, Crassulaceae, Dioscoreaceae, Ebenaceae, Elaeagnace-
ae, Euphorbiaceae, Fabaceae, Loranthaceae, Malpighiaceae, Malvaceae, Melastomace-
ae, Myrsinaceae, Myrtaceae, Olacaceae, Pinaceae, Polygonaceae, Proteaceae, Rham-
naceae, Rosaceae, Rubiaceae, Rutaceae, Santalaceae, Sapindaceae, Sterculiaceae, Thy-
melaceae, Verbenaceae, Zygophyllaceae; attended by ants, and some may feed addi-
tionally on ant regurgitations, or perhaps even ant brood.
Spindasis Wallengren, 1857

(silverlines — not illustrated)
Range (P).–– Afrotropical and Oriental Regions, extending to China, Japan, Malay
Peninsula, Sumatra, Java, Borneo, Philippines and the Sulawesi Region (Buton). Well
over 30 species are known, with about six occurring in the Malay Archipelago.
Foodplants.–– Asteraceae, Capparaceae, Combretaceae, Convolvulaceae, Diosco-
reaceae, Eleagnaceae, Euphorbiaceae, Fabaceae, Loranthaceae, Malpighiaceae, Mal-
vaceae, Melastomaceae, Myrtaceae, Olacaceae, Pinaceae, Proteaceae, Rhamnaceae,
Rosaceae, Rubiaceae, Rutaceae, Santalaceae, Sapindaceae, Verbenacae, Zygophyllace-
ae; attended by ants.
Key works.–– Corbet & Pendlebury (1992), d’Abrera (1986), Seki et al. (1991).
S. vulcanus Fabricius, 1775

(Common Silverline)
Range (P).–– Sri Lanka, India, Burma, Thailand, Java, Buton.
Foodplants.–– Cadaba (Capparaceae); Ziziphus (Rhamnaceae); Canthium (Rubiace-
ae); Allophylus (Sapindaceae); Clerodendrum (Verbenaceae) (all from India: Bell, 1919);
always and obligately associated with Crematogaster (Formicidae).
–– *S. vulcanus subsp. (Jurriaanse & Lindemans, 1920).
Range.–– Buton.
Iolaini Verity, 1943

(royals, imperials — Pl. 7, figs 16-18)
Range.–– Palaeotropics. A large group with at least 16 genera in the Oriental

Region, of which only three are found on Sulawesi.

Foodplants.–– Fabaceae, Hydrangeaceae, Loranthaceae, Olacaceae.
Tajuria Moore, 1881

(royals — Pl. 7, fig. 16)
Range (1+2+6+7).–– Sri Lanka to Taiwan, Java, Philippines and Sulawesi. A

somewhat heterogeneous assemblage of about 40 species, four of which are known to
occur on Sulawesi.
Foodplants.–– Fabaceae, Hydrangeaceae, Loranthaceae.
Key works.–– Corbet & Pendlebury (1992), d’Abrera (1986), Takanami (1989), Seki
et al. (1991), Seki (1997).
T. mantra Felder & Felder, 1860

(Felder’s Royal)
Range (1+2+6+7).–– Burma, Malay Peninsula, Sumatra, Java, Borneo, Palawan
(Treadaway, 1995), Philippines, Sulawesi Region.
Foodplants.–– Dendrophthoe, Scurrula (Loranthaceae). Igarashi & Fukuda (2000)
illustrate the pupa.
–– *T. mantra jalysus Felder & Felder, 1865
Range.–– Sulawesi, Kep. Banggai.
*T. cyrillus Hewitson, 1865

(Pl. 7, fig. 16)
*T. species (BMNH; d’Abrera, 1986)

Range (E).–– Sulawesi (C: Palu region).
*T. iapyx Hewitson, 1865

Range (R).–– Sulawesi Region, ?Maluku.
–– *T. iapyx iapyx Hewitson, 1865
–– *T. iapyx bangkaianus Ribbe, 1926
–– *T. iapyx subsp. (BMNH)
Range.–– Kep. Tukangbesi (Kaledupa).
–– *T. iapyx subsp. (BMNH)
Pratapa Moore, 1881

(not illustrated — cf. Pl. 7, fig. 17)
Range (1+2+5+6+7).–– Sri Lanka, India, China, Malay Peninsula, Greater and Les-
ser Sundas, Palawan, Philippines (Treadaway, 1995), Sulawesi. Six species (Seki, 1997).
Key works.–– d’Abrera (1986), Seki (1997).
*P. cameria de Nicéville, 1898

Paruparo Takanami, 1982

(not illustrated — cf. Pl. 7, fig. 17)
Range (1+2+6+7).–– Sri Lanka, India, Malay Peninsula, Sumatra, Java, Borneo, Phi-
lippines and Sulawesi Region. A group of about a dozen species, several of which
have only recently been described from the Philippines, where the genus is most well
represented; a single very rare species occurs in the Sulawesi Region.
Note.–– Seki & Takanami (1990) moved the Sulawesi species from Eliotia Hayashi
1978 (=Rachana Eliot, 1978; Eliotia Hayashi preoccupied) to Paruparo Takanami, 1982.
The generic placement of species in Paruparo, Rachana (and possibly Pratapa and Elio-
tiana: Eliot & Kirton, 2000) needs clarification. Treadaway (1995) lists several Rachana
(as Eliotia) and several Paruparo from the Philippines. A species from the Andaman
islands that has been placed in Rachana is illustrated on Pl. 7 (fig. 17).
Foodplants.–– Loranthaceae (Loranthus).
Key works.–– Hayashi (1978), Eliot in Corbet & Pendlebury (1978), d’Abrera
(1986), Seki & Takanami (1990).
*P. kuehni Röber, 1887

–– *P. kuehni regulus Staudinger, 1888
–– *P. kuehni birumki Ribbe, 1926
–– *P. kuehni kuehni Röber, 1887
Dacalana Moore, 1884

Range (1+2+6+7).–– Northern India to Java, Philippines and Sulawesi Region. A

group of about 20 species, well represented in the Philippines (there have been several
recent discoveries), and by three species in the Sulawesi Region.
Foodplants.–– Loranthaceae.
Key works.–– Eliot (1962), Corbet & Pendlebury (1992), d’Abrera (1986), Takanami
(1989).
*D. anysis Hewitson, 1865

(Pl. 7, fig. 18)
Foodplants.–– Scurrula (Loranthaceae). Igarashi & Fukuda (1997, 2000) illustrate
the foodplant, larva and pupa.
–– *D. anysides Röber, 1887

*D. sangirica Fruhstorfer, 1912

Range (L).–– Kep. Sangihe, Kep. Talaud.
Remelanini Eliot, 1973

Range.–– Oriental Region, Wallacea and Lesser Sunda Islands. A small tribe
comprising three genera, one of which occurs in Sulawesi.
Foodplants.–– Bombacaceae, Ericaceae, Euphorbiaceae, Fabaceae, Hypericaceae,
Loranthaceae, Myrsinaceae, Rubiaceae, Sapindaceae, Sterculiaceae, Verbenaceae.
Remelana Moore, 1884

Range (1+2+5+6+7).–– Oriental Region, except Sri Lanka and southern India,
extending to Palawan, Philippines, Sulawesi and Lesser Sunda Islands. Two species,
one very widespread, the other restricted to the Philippines (see Treadaway, 1995).
Foodplants.–– Bombacaceae (Durio: Kuroko & Lewvanich, 1993); Ericaceae (Rho-
dodendron); Euphorbiaceae (Bascombe et al., 1999); Fabaceae (gen. indet.: K. Fiedler,
pers. obs. in Borneo); Hypericaceae; Myrsinaceae; Myrtaceae (Cleistocalyx: Young,
1998); Rhizophoraceae (Kandelia: Young, 1998); Rubiaceae, Sapindaceae (Litchi:
Young, 1998), Sterculiaceae; Theaceae (Eurya: Young, 1998); Verbenaceae (Bascombe
et al., 1999); facultatively attended by ants (e.g. Anoplolepis in Borneo, Polyrachis in
Hong Kong).
R. jangala Horsfield, 1829

(Chocolate Royal — Pl. 7, fig. 19)
Range (1+2+5+6+7).–– As genus.
Foodplants.–– As genus. Young (1998) illustrates all life stages (Hong Kong).
–– *R. jangala orsolina Hewitson, 1865
Hypolycaenini Swinhoe, 1910

(tits — Pl. 7, fig. 20)
Range.–– Afrotropical and Oriental Regions, extending to Australia. Well repre-

sented in Africa, with one genus in Indo-Australia (Fiedler, 1992a, regards Chliaria
Moore and Zeltus de Nicéville as synonymous with Hypolycaena).
Foodplants.–– Aizoaceae, Bignoniaceae, Bombacaceae, Clusiaceae, Combretaceae,
Connaraceae, Crassulaceae, Cucurbitaceae, Fabaceae, Flagellariaceae, Lauraceae, Lecy-
thidaceae, Loganiaceae, Loranthaceae, Meliaceae, Myrsinaceae, Myrtaceae, Olacacaeae,
Opiliaceae, Orchidaceae, Proteaceae, Punicaceae, Rhamnaceae, Rhizophoraceae,

Rubiaceae, Sapindaceae, Smilacaceae and Verbenaceae; sometimes or always attended
by ants (Fiedler, 1991, 1992a).
Key works.–– Eliot (1973), Corbet & Pendlebury (1992), Takanami (1989), Larsen
(1991), Fiedler (1991).
Hypolycaena Felder & Felder, 1862

(tits — Pl. 7, fig. 20)
Range (W).–– As tribe. About 25 species in the Indo-Australian region (Fiedler,

1992a), of which 4 are found on Sulawesi, and about 20 species in Africa (Ackery et al.,
1995).
Foodplants.–– As tribe, except not recorded from Aizoaceae or Crassulaceae,
sometimes or always attended by ants (e.g. Camponotus, Crematogaster, Oecophylla,
Polyrhachis).
Key works.–– Common & Waterhouse (1981), d’Abrera (1986), Fiedler (1991,
1992a), Corbet & Pendlebury (1992).
H. erylus Godart, 1824

(Common Tit)
Range (W).–– Northern India, Indo-China, Malay Peninsula, Sumatra, Java, Lesser
Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region, Maluku, New Guinea
region.
Foodplants.–– Ceiba (Bombacaceae); Lumnitzera (Combretaceae); Agelaea (Conna-
raceae); Acacia, Paraserianthes, Saraca (Fabaceae); Garcinia (Clusiaceae: Igarashi & Fuku-
da, 2000); Cinnamomum (Lauraceae); Fagraea (Loganiaceae); Dendrophthoe, Helixanthera
(Loranthaceae); Sandoricum (Meliaceae); Eugenia (Myrtaceae); Champereia (Opiliaceae);
Dimocarpus (Sapindaceae: Kuroko & Lewvanich, 1993); Macadamia (Proteaceae); Zizip-
hus (Rhamnaceae); Bruguiera, Rhizophora (Rhizophoraceae); Ixora, Nauclea (Igarashi &
Fukuda, 2000), Scyphiphora (Seufert, 1997), Vangueria (Rubiaceae); Clerodendron (Verbe-
naceae); always attended by ants (Oecophylla smaragdina; Fiedler, 1996b). Igarashi &
Fukuda (2000) illustrate the larvae attended by ants, and the pupa.
–– * H. erylus gamatius Fruhstorfer, 1912
Range.–– Sulawesi, Kep. Talaud, Kep. Sangihe (Siao), Kep. Tukangbesi, Kep. Sula
(Mangole).
*H. umbrata Seki & Takanami, 1988

H. sipylus Felder, 1860 (= lewara Ribbe, kalawara Ribbe)

(Pl. 7, fig. 20)
Range (1+2+3+4+5+6).–– Eastern Java, Lesser Sunda Islands, Balabac, Palawan,
Philippines, Sulawesi Region, N & C Maluku, ?New Guinea (not noted in Parsons,
1999); no record for Borneo (Seki et al., 1991).
Foodplant.–– Eugenia (Myrtaceae: Semper 1890), recorded as tharrytas from Mani-
la. Igarashi & Fukuda (2000), who illustrate the early stages and the larva attended by
ants, report the larvae from ornamental Ixora (Rubiaceae) in the Philippines.
–– *H. sipylus giscon Fruhstorfer, 1912
Range.–– Sulawesi, Tanahjampea, Kalao, Kep. Tukangbesi, Kep. Banggai (Peleng),
Kep. Sula (Mangole, Sanana).
*H. xenia Grose Smith, 1895 (= celebica Ribbe, J. N. Eliot, pers. comm.)
Deudorigini Doherty, 1886

(cornelians, planes, flashes — Pl. 7, figs 21-25)
Range.–– Afrotropical and Oriental, extending weakly into Palaearctic and Austra-
lian Regions. A large grouping which includes eight genera in the Oriental Region,
five of which are found on Sulawesi.
Foodplants.–– Aitoniaceae, Anacardiaceae, Apiaceae, Arecaceae, Caprifoliaceae,
Celastraceae, Combretaceae, Connaraceae, Elaeocarpaceae, Eleagnaceae, Ericaceae,
Euphorbiaceae, Fabaceae, Fagaceae, Hippocastanaceae, Hippocrateaceae, Loganiace-
ae, Loranthaceae, Lythraceae, Melastomataceae, Myrtaceae, Olacaceae, Oleaceae, Oxa-
lidaceae, Pinaceae, Piperaceae, Pittosporaceae, Poaceae, Proteaceae, Punicaceae,
Rhamnaceae, Rosaceae, Rubiaceae, Rutaceae, Sapindaceae, Sapothaceae, Saxifragace-
ae, Solanaceae, Symplocaceae, Theaceae, Verbenaceae.
Bindahara Moore, 1881

(planes — Pl. 7, fig. 21)
Range (1+2+4+5+6+7).–– Oriental and Australian Regions, from Sri Lanka to Aus-
tralia and the Solomon Islands. Three species, one of which occurs on Sulawesi.
Foodplants.–– Celastraceae (Celastris, Euonymus, Salacia; larvae in fruits), Rham-
naceae. Ant-associations not recorded.
Key works.–– Corbet & Pendlebury (1992), Common & Waterhouse (1981).
B. phocides Fabricius, 1793

(Plane — Pl. 7, fig. 21)
Range (1+2+4+5+6+7).–– As genus, including Malay Peninsula, Sumatra, Java,
Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region and C Maluku
(Buru).
Foodplants.–– As genus. Igarashi & Fukuda (2000) illustrate all life stages.
–– *B. phocides fumata Röber, 1887
Range.–– Sulawesi, Kep. Talaud, Kep. Banggai, Kep. Sula (Mangole, Sanana).
Rapala Moore, 1881

(flashes — Pl. 7, fig. 22)
Range (W).–– Oriental Region, extending eastwards into Palaearctic and Austra-
lian Regions. A genus of about 30 or more species, often very local, with six occurring
on Sulawesi; Takanami (1998) lists 28 species from “the southeast Asian Islands”.
Foodplants.–– Anacardiaceae, Annonaceae, Caprifoliaceae, Combretaceae, Conna-
raceae, Elaeagnaceae, Ericaceae, Euphorbiaceae, Fabaceae, Fagaceae, Lythraceae,
Melastomataceae, Myrtaceae, Oleaceae, Oxalidaceae, Piperaceae, Rhamnaceae, Ros-
aceae, Sapindaceae, Saxifragaceae, Symplocaceae, Theaceae, Ulmaceae, Verbenaceae.
Attended by ants (e.g. Iridomyrmex), either facultatively or in obligate relationship
(Fiedler, 1996b).
Key works.–– d’Abrera (1977, 1986), Corbet & Pendlebury (1992), Common &
Waterhouse (1981), Takanami (1989, 1992a, 1998), Seki et al. (1991).
*R. ribbei Röber, 1886

*R. dioetas Hewitson, 1869 (? = zylda Seitz, [1922])

(Pl. 7, fig. 22 — zylda)
Range (R).–– Sulawesi, Kep. Sangihe, Kep. Talaud, Kep. Banggai, Salayar.
Foodplants.–– Lagerstroemia (Lythraceae) (recorded by Igarashi & Fukuda, 1997,
who also illustrate larva and pupa).
*R. enipeus Staudinger, 1888 (= cindy d’Abrera, 1986)

Range (R).–– Sulawesi, Salayar, Kep. Banggai, Manui (Takanami, 1992a).
*R. cassidyi Takanami, 1992

R. manea Hewitson, 1863

(Slate Flash)
Range (1+2+5+6+7).–– Sri Lanka, India, southern China, Malay Peninsula, Suma-
tra, Java, Lesser Sunda Islands, Borneo, Palawan (Treadaway, 1995), Philippines, Sula-
wesi Region.
Foodplants.–– Mangifer (Anacardiaceae); Viburnum (Caprifoliaceae); Quisqualis
(Combretaceae: Wynter Blyth 1982, under R. schistacea from India); Antidesma (Eup-
horbiaceae); Acacia, Albizia, Bauhinia, Lasiobema, Millettia, Pueraria (Fabaceae); Lithocar-
pus (Fagaceae); Jasminum (Bascombe et al., 1999) (Oleaceae); Ziziphus (Rhamnaceae);
Photinia, Sorbaria, Spiraea (Rosaceae); Nephelium, Dimocarpus (Kuroko & Lewvanich,
1993) (Sapindaceae); Camellia, Gordonia (Theaceae); Lantana (Verbenaceae). Igarashi &
Fukuda (1997) illustrate larva and pupa.
–– *R. manea manea Hewitson, 1863
Range.–– Sulawesi, Kep. Talaud, Salayar, Tanahjampea, Kalao, Buton, Kep. Bang-
gai (Peleng), Kep. Sula (Mangole).
R. varuna Horsfield, 1829

(Indigo Flash)
Range (W).–– Sri Lanka, India, Taiwan, Malay Peninsula, Sumatra, Java, Lesser
Sunda Islands, Borneo, Palawan, Philippines, Sulawesi, N & C Maluku, New Guinea
region, Australia.
Foodplants.–– Quisqualis (Combretaceae); Acacia, Dendrolobium (Fabaceae); Psidium

(Myrtaceae); ?Buckinghamia (Proteaceae); Alphitonia, Zizyphus (Rhamnaceae); Litchi,
Sapindus (Wynter Blyth, 1982; from India), Nephelium (Kuroko & Lewvanich, 1993)
(Sapindaceae); Gordonis (Theaceae); Celtis (Ulmaceae: Shen-Horn Yen in litt., from Tai-
wan); Verbenaceae.
–– *R. varuna olivia Druce, 1895
Deudorix Hewitson, 1863

(cornelians, playboys — Pl. 7, fig. 23)
Range (W).–– Oriental, Australian and Pacific Regions, from Sri Lanka to Samoa;
also Afrotropical Region. A genus of about 35 species (excluding the African mem-
bers, many of which are often placed in the genus or subgenus Virachola Moore, 1881),
with three occurring on Sulawesi.
Foodplants.–– Aitoniaceae, Apiaceae, Arecaceae, Celastraceae, Combretaceae, Con-
naraceae, Elaeocarpaceae, Euphorbiaceae, Fabaceae, Hippocastanaceae, Loganiaceae,
Loranthaceae, Lythraceae, Myrtaceae, Olacaceae, Pinaceae, Pittosporaceae, Poaceae,
Proteaceae, Punicaceae, Rosaceae, Rubiaceae, Rutaceae, Sapindaceae, Sapotaceae, Sola-
naceae, Theaceae. Larvae of most species only occasionally attended by ants.
Key works.–– d’Abrera (1977, 1986), Corbet & Pendlebury (1992), Common &
Waterhouse (1981).
*D. cleora Miller & Miller, 1986

(Millers’ Playboy)
Note.–– Known only from the holotype, preserved in the Allyn Museum, this stri-
king species was discovered in the Tondano area in 1940.
D. epijarbas Moore, 1858

(Cornelian — Pl. 7, fig. 23)
Range (W).–– As genus, including Malay Peninsula, Sumatra, Java, Lesser Sunda
Islands, Borneo, Palawan, Philippines, Sulawesi Region and N & C Maluku.
Foodplants.–– Typically fruits belonging to a variety of families, including Are-
caceae; Connarus (Connaraceae); Elaeocarpus (Elaeocarpaceae); Drypetes, Euphorbia,
Phyllanthes (Euphorbiaceae); Bauhinia, Cynometra (Fabaceae); seed capsules of Aesculus
(Hippocastanaceae); Pinus (Pinaceae); Panicum (Poaceae); Proteaceae; Punica (Puni-
caceae); Dimocarpus, Euphoria, Lepisanthes, Litchi, Nephelium, Sapindus (Sapindaceae).
Igarashi & Fukuda (1997) illustrate larva and pupa.
–– *D. epijarbas megakles Fruhstorfer, 1911
Range.–– Sulawesi, Kep. Talaud, Kalao, Kep. Banggai.
*D. loxius Hewitson, 1869

Artipe Boisduval, 1870

(green flashes — Pl. 7, fig. 24)
Range (7).–– Northern India, China, Indo-China, Malay Peninsula, Taiwan, Bor-
neo, Sulawesi and New Guinea region: not known from Sumatra, Java, Lesser Sunda
Islands, Philippines and Maluku. A small genus (about six species; Parsons 1999) with
a curious distribution; one of the species reaches southern Sulawesi.
Foodplants.–– ?Lythraceae, Rubiaceae.
Key works.–– d’Abrera (1977, 1986), Corbet & Pendlebury (1992).
A. eryx Linnaeus, 1771

(Green Flash — Pl. 7, fig. 24)
Range (7).–– As genus.
Foodplants.–– ?Lythraceae (Fiedler, 1991); fruits of Gardenia, Randia (Rubiaceae).
Osada (1997) illustrates Randia and the damage done to the fruits by Artipe.
–– *A. eryx alax Eliot, 1956
Sinthusa Moore, 1884

(sparks — Pl. 7, fig. 25)
Range (1+2+6+7).–– Oriental Region, from northern India to Taiwan and Java to
Palawan, Philippines and Sulawesi; absent from Maluku and the Lesser Sunda
Islands. A group of about a dozen species, at least two of which occur on Sulawesi.
Foodplants.–– Rosaceae (Rubus).
*S. verriculata Snellen, 1892

(Pl. 7, fig. 25)
Range (R).–– Sulawesi (SE), Kep. Banggai (Peleng), ?Kep. Sula (Sanana).
Note.–– The nominal taxon verena Grose Smith is treated here as a synonym of ver-
riculata, but this needs confirmation; two males in BMNH from Sanana may represent a
further species.
*S. indrasari Snellen, 1878

Polyommatinae Swainson, 1827

(blues and coppers — Pl. 8)
Range.–– The Polyommatinae are a very large, cosmopolitan group of well over
1000 species, divided into four unequal tribes of which only the largest, the Polyom-
matini, and the Lycaenesthini (represented by Anthene) occur in the Sulawesi Region.
Foodplants.–– Many families of plants, including Aizoaceae, Amaranthaceae,
Boraginaceae, Cycadaceae, Euphorbiaceae, Fabaceae, Loranthaceae, Malpighiaceae,
Meliaceae, Oxalidaceae, Plumbaginaceae, Proteaceae, Rhamnaceae, Rubiaceae, Ruta-
ceae, Sapindaceae, Ulmaceae, Urticaceae, Verbenaceae, Zingiberaceae, Zygophyllace-

ae. Some Polyommatini are associated with ants.
Key works.–– Eliot (1973), d’Abrera (1977, 1986), Corbet & Pendlebury (1992),
Hirowatari (1992).
Lycaenesthini Toxopeus, 1929

(ciliate blues, hairtails — Pl. 8, fig. 1)
Range.–– Palaeotropics (mainly African). Seven genera are included, of which

only one is represented in the Indo-Australian Region.
Foodplants.–– Anacardiaceae, Combretaceae, Connaraceae, Crassulaceae, Escallo-
niaceae, Euphorbiaceae, Fabaceae, Fagaceae, Flagellariaceae, Lauraceae, Loranthaceae,
Lythraceae, Malpighiaceae, Meliaceae, Melianthaceae, Myricaceae, Myrtaceae, Rosace-
ae, Rubiaceae, Sapindaceae, Smilacaceae, Sterculiaceae, Ulmaceae, Verbenaceae.
Anthene Doubleday, 1847

(ciliate blues, hairtails — Pl. 8, fig. 1)
Range (W).–– Palaeotropics. A large genus (ca 100 species), about 10 of which
occur in the Indo-Australian region, four of them on Sulawesi.
Foodplants.–– As tribe (except Loranthaceae); attended by ants (Oecophylla), at
least some species in obligate relationships (Fiedler, 1996b).
Key works.–– Tite (1966), Corbet & Pendlebury (1992).
A. lycaenina Felder, 1868

Range (1+2+5+6+7).–– Sri Lanka to Malay Peninsula, Lombok, Palawan, Philip-
pines (Treadaway, 1995), Sulawesi Region.
Foodplants.–– Buchanania (Anacardiaceae); Caesalpinia (Fabaceae).
–– *A. lycaenina subsp.
Range.–– Sulawesi, Kep. Banggai (Peleng) (Seki et al., 1991: 47).
A. paraffinis Fruhstorfer, 1916

Range (P).–– Kep. Sula, Maluku, New Guinea, Bismarcks, Solomon Islands.
Foodplants.–– ?Saraca (Fabaceae; Parsons, 1999).
–– A. paraffinis emoloides Tite, 1966
Range.–– Kep. Sula, C Maluku (Buru), New Guinea.
*A. philo Hopffer, 1874

–– *A. philo philo Hopffer, 1874
Range.–– Sulawesi, Salayar, Kep. Tukangbesi, Kep. Banggai, Kep. Sula.
–– *A. philo scintillans Tite, 1966
Range.–– Kep. Sangihe, Kep. Talaud.
*A. lycaenolus Tite, 1966

Range (L).–– Kep. Talaud.
A. licates Hewitson, 1874

(Pl. 8, fig. 1)
Range (1+3).–– Malay Peninsula, Sumatra, Palawan, Sanga Sanga (Treadaway,
1995), Sulawesi, Kep. Banggai, Maluku (Obi), New Guinea.
–– *A. licates licates Hewitson, 1874
*A. villosa Snellen, 1878

Range (R).–– Sulawesi, Kep. Sangihe (Sangihe, Siao), Kep. Talaud.
Polyommatini Swainson, 1827

(blues — Pl. 8, figs 2-35)
Range.–– A vast, cosmopolitan assemblage, comprising most of the Polyom-

matinae. Over 30 genera are represented on Sulawesi.
Foodplants.–– Including (in the Oriental Region), Aizoaceae, Amaranthaceae,
Boraginaceae, Cycadaceae, Euphorbiaceae, Fabaceae, Malpighiaceae, Meliaceae, Oxa-
lidaceae, Plumbaginaceae, Proteaceae, Rhamnaceae, Rubiaceae, Rutaceae, Sapindace-
ae, Ulmaceae, Urticaceae, Zingiberaceae, Zygophyllaceae.
Key works.–– Eliot (1973), Corbet & Pendlebury (1992), Eliot & Kawazoé (1983),
Hirowatari (1986b).
Cupidopsis Karsch, 1895

(meadow blues — not illustrated)
Range.–– Afrotropical Region, including Madagascar and Yemen, with one of the
three species anomalously recorded from Sulawesi (see below).
Foodplants (in Afrotropics).–– Flowers, buds and seed pods of Fabaceae (Eriosema,
Rhynchosia, Vigna); attended by ants.
Key works.–– d’Abrera (1980), Ackery et al. (1995).
C. jobates Hopffer, 1855

(Tailed Meadow Blue)
Range.–– Africa. Tennent (1996a) gives an account of the collection of a male speci-
men from a locality near Molibagu, Sulawesi Utara, during the 1985 Royal Entomolo-
gical Society of London Project Wallace expedition. This apparently genuine record
remains unexplained. In the rather unlikely event that this species does prove to be
established on Sulawesi, plausibly it was introduced from Africa in seedpods of a
forage plant such as Vigna (cowpea).
Foodplants (in Afrotropics).–– Eriosema, Rhynchosia (Fabaceae).
Una de Nicéville, 1890

(singeltons — Pl. 8, fig. 2)
Range (2+6+7).–– Assam, Hainan, Malay Peninsula, Sumatra, Java, Borneo, Philip-
pines (Mindanao), Sulawesi (C: Takanami, 1986b). One or two species.
Key works.–– Schroeder & Treadaway (1986), Corbet & Pendlebury (1992), Hiro-
watari (1992).
U. usta Distant, 1886

(Singleton — Pl. 8, fig. 2)
Range (6+7).–– As genus.
–– U. usta usta Distant, 1886
Range.–– As genus (including central Sulawesi), except Java and Philippines.
According to Treadaway (1995), the Mindanao population represents a separate spe-
cies (U. philippensis Schröder & Treadaway, 1986), but Hirowatari (1992) considered
Una to be monobasic.
Petrelaea Toxopeus, 1929

(dingy lineblues — Pl. 8, fig. 3)
Range (1+2+3+6+7).–– Chagos Archipelago, Sri Lanka, India, Assam, Andaman

Islands, Malay Peninsula, Sumatra, Java, Borneo, Palawan, Philippines (Mindanao:
Treadaway, 1995), Sulawesi, N & ?S Maluku, New Guinea, Bismarcks, northern
Australia, Solomon Islands. Two species.
Key works.–– Tite (1963), Corbet & Pendlebury (1992), Common & Waterhouse
(1981), Fujioka & Chiba (1988), Hirowatari (1992), Parsons (1999).
P. tombugensis Röber, 1886

(Eastern Dingy Lineblue - cf. Pl. 8, fig. 3)
Range (3).–– Andaman Islands, ?Palawan, Sulawesi (N, E: Cassidy, 1990), Kep.
Sula (Mangole), N Maluku (Bacan, Obi), New Guinea, Solomon Islands (Tennent,
2002), North Australia (Hirowatari, 1992), Ogasawara Islands (Hirowatari, 1992).
Note.–– This distribution is based largely on Fujioka & Chiba (1988), but Hirowa-
tari (1992) does not list the Andamans, describing tombugensis as a species “distributed
eastward of Sulawesi” (sic); it is likely that this recently separated species will be
recognised from a wider range of localities in future. Parsons (1999), following Fujioka
& Chiba, considered that the two species were sympatric in the Andamans.
Nacaduba Moore, 1881

(lineblues — Pl. 8, figs 4, 5)
Range (W).–– Oriental, Australian and Pacific Regions, from Sri Lanka to Samoa
and Tahiti. A large genus of 40 species (Hirowatari, 1992), at least 12 of which occur in
the Sulawesi Region (Cassidy, 1990).
Foodplants.–– Anacardiaceae, Dipterocarpaceae, Fabaceae, Myrsinaceae, Primu-
laceae, Proteaceae, Sapindaceae, Sapotaceae, Sterculiaceae, Ulmaceae; attended by
ants (Iridomyrmex, Prolasius).
Key works.–– Eliot (1955), Tite (1963), Corbet & Pendlebury (1992), Common &
Waterhouse (1981), d’Abrera (1986), Hirowatari (1986b, 1990, 1992), Takanami (1990,
1992b), Cassidy (1990).
N. angusta H. Druce, 1873

(White Lineblue — Pl. 8, fig. 5)
Range (1+2+6+7).–– India, Burma, Thailand, Indo-China (Hirowatari, 1992), Malay
Peninsula, Sumatra, Java, Borneo, Palawan, Philippines, Sulawesi Region.
–– *N. angusta pamela Grose Smith, 1895
Range.–– Sulawesi (N, C, S), Kep. Banggai (Peleng), Kep. Sula (Sanana, Mangole).
–– *N. angusta sangira Fruhstorfer, 1916
Takanami (1992b) points out that the name azureus Röber was for long misapplied
to this species; on transfer of azureus to N. pavana, the senior name available for N.
angusta from Sulawesi is N. pamela.
N. pactolus Felder, 1860

(Large 4-lineblue)
Range (1+2+4+5+6+7).–– Sri Lanka, India, south China, Taiwan, Burma, Thailand,
Indo-China, Malay Peninsula, Sumatra, Java, Lesser Sunda Islands (Takanami, 1986a),
Borneo, Palawan, Philippines, Sulawesi Region, C Maluku (Hirowatari, 1992), New
Guinea region (including Aru: Takanami, 1992b), Solomon Islands (Tennent, 2002).
Foodplants.–– Entada (Fabaceae: Bean, 1964); Embelia (Myrsinaceae: Wynter Blyth,
from India). Facultatively attended by ants (e.g. Camponotus).
–– *N. pactolus pactolides Fruhstorfer, 1916
Range.–– Sulawesi (N, C, S), Kep. Banggai, Kep. Talaud, Kep. Sula (Sanana).
N. pavana Horsfield, 1828

(Small 4-lineblue)
Range (1+2+6+7).–– India, Burma, Malay Peninsula, Sumatra (Hirowatari, 1992),
Java, Borneo (Seki et al., 1991; Hirowatari, 1992), Palawan, Philippines (Leyte, Sibuyan,
Mindanao: Treadaway, 1995), Sulawesi.
–– *N. pavana azureus Röber, 1886
Range.–– Sulawesi (N, C, E).
Takanami (1992b) explains the transfer of the name azureus Röber from N. angusta,
to which species it was previously considered to refer, and the consequent synonymy
of N. pavana visuna Fruhstorfer.
N. hermus Felder, 1860

Range (W).–– Sri Lanka and India to Borneo (Seki et al., 1991), Java, Lombok, Phi-
lippines, Sulawesi, Maluku, New Guinea (Parsons, 1999).
Foodplants.–– Lannea (Anacardiaceae); Pongamia (Fabaceae).
–– N. hermus hermus Felder 1860
Range.–– Sulawesi (Morowali District: Cassidy, 1990), Maluku (Obi, Seram, Ambon).
N. subperusia Snellen, 1896

(Violet 4-lineblue)
Range (1+2+3+5+6+7).–– Assam, Malay Peninsula, Sumatra, Java, Sumba (Seki et al.,
1991), Borneo, Palawan, Philippines, Sulawesi Region, Maluku, New Guinea region.
–– N. subperusia paska Eliot, 1955
Range.–– Palawan, Philippines (Treadaway, 1995), Sulawesi (N: Cassidy, 1990),

Kep. Sula (Sanana), N Maluku.
N. sanaya Fruhstorfer, 1916

Range (2+3+4+6+7).–– India, Burma, Malay Peninsula, Sumatra, Java, Borneo,
Philippines (excluding Palawan: Treadaway, 1995), Sulawesi, Maluku (no details:
Hirowatari, 1992).
–– N. sanaya metallica Fruhstorfer, 1916
Range.–– Philippines, Sulawesi (N), ?Kep. Banggai.
*N. angelae Cassidy, 1990

N. berenice Herrich-Schäffer, 1869

(Rounded Six Lineblue — Pl. 8, fig. 4)
Range (W).–– Oriental and Australian Regions, from Sri Lanka, N & C Maluku to
the Solomon Islands, including Australia.
Foodplants.–– Calliandra, Wagatea (Fabaceae); Macadamia (Proteaceae); Alectryon,
Cupaniopsis, Heterodendron (Sapindaceae); Theobroma (Sterculiaceae; Fujii, 1987); Apha-
nanthe (Ulmaceae; Braby, 2000).
–– *N. berenice eliana Fruhstorfer, 1916
Range.–– Sulawesi, Kep. Banggai (Peleng), Kep. Sula.
–– N. berenice zyrthis Fruhstorfer, 1916
Range.–– Java, Lesser Sunda Islands east to Banda, Tanahjampea, Kalao.
N. normani Eliot, 1969

(Norman’s Lineblue)
Range (7).–– Borneo, Sulawesi.
Foodplants.–– Bauhinia (Fabaceae); Paranephelium (Sapindaceae); Theobroma (Ster-
culiaceae) (Pan & Morishita, 1990).
–– *N. normani titei Eliot, 1969
N. kurava Moore, 1858

(Transparent 6-lineblue)
Range (1+2+4+5+6+7).–– Widespread throughout Oriental and Australian Regions,
including Palawan and Mindanao (Philippines) and C Maluku.
Foodplants.–– Dipterocarpaceae; Pueraria (Fabaceae); Aegiceras, Ardisia, Embelia,
Maesa, Myrsine, Rapanea (Myrsinaceae); Lysimachia (Primulaceae); Cupaniopis, Nepheli-
um (Sapindaceae). Igarashi & Fukuda (1997) illustrate larva and pupa.
–– *N. kurava menyangka Takanami, 1990
Range.–– Sulawesi (N, C, S), Kep. Talaud, Kep. Banggai (Peleng), Kep. Sula (Sanana).
Cassidy (1990) argues that the geographical distribution of phenotypes precludes
division of N. kurava into subspecies in the Sundaland-Philippines-Sulawesi part of
the species’ range, and includes Sulawesi material in the nominotypical subspecies
(type locality Java). However, we here tentatively accept the taxon introduced by
Takanami (1990), described from C and S Sulawesi, for the Sulawesi Region.
N. beroe Felder & Felder, 1865

(Opaque 6-lineblue)
Range (1+2+5+6+7).–– Widespread in Oriental Region, Malay Peninsula, Sumatra,
Java, Bali, Sumba (Seki et al., 1991), Borneo, Palawan, Philippines (Treadaway, 1995),
Sulawesi, Kalao.
Foodplants.–– Fabaceae.
–– *N. beroe hayashii Takanami, 1990
Range.–– Sulawesi (N, C, S), Kalao (Cassidy, 1990).
N. calauria Felder, 1860

(Dark Ceylon 6-lineblue)
Range (P).–– Sri Lanka, India (Hirowatari, 1992), Malay Peninsula, Sumatra, Java,
Sumbawa, Flores (Takanami, 1986a), Borneo, ?Philippines (not included by Treadaway,
1995), Kep. Sula (Cassidy, 1990), Maluku, New Guinea, New Britain (Seki et al., 1991).
–– N. calauria calauria Felder, 1860
Range.–– Kep. Sula, N & C Maluku, New Guinea, ?New Britain.
Psychonotis Toxopeus, 1930

(green-banded blues — Pl. 8, fig. 12)
Range (3+4).–– A genus of nine species (Hirowatari, 1992), most richly represented
in the Papuan Region but extending into Australia, Maluku and Sulawesi.
Foodplants.–– Rhamnaceae (Alphitonia).
Key works.–– d’Abrera (1977), Common & Waterhouse (1981), Hirowatari (1992).
*P. piepersii Snellen, 1878

(Pl. 8, fig. 12)
Range (E).–– Sulawesi, Kep. Banggai (Peleng), Kep. Sula (Sanana).
Prosotas H.H. Druce, 1891

(lineblues — Pl. 8, fig. 6)
Range (W).–– Oriental and Australian Regions. One third of the 18 or so known
species are found in the Sulawesi Region.
Foodplants.–– Combretaceae, Fabaceae, Myrtaceae, Proteaceae, Sapindaceae;
sometimes ant attended.
(1981), d’Abrera (1986), Hirowatari (1992).
P. aluta H. Druce, 1873

(Banded Lineblue)
Range (1+2+5+6+7).–– Sikkim, Assam, Thailand, Malay Peninsula, Sumatra, Java,
Sumbawa, Dammar (Seki et al., 1991), Borneo, Palawan, Philippines, Sulawesi Region.
Foodplant.–– Dalbergia (Veenakumari et al., 1998); gen. indet. (Fiedler, pers. obs. in
Sabah, Borneo) (Fabaceae) – facultatively attended by ants (Anoplolepis).
–– *P. aluta alutina Fruhstorfer, 1916
Range.–– Sulawesi (N), Kep. Banggai (Peleng). Cassidy (1990) reports that this but-
terfly was not rediscovered during the 1985 Project Wallace expedition to N Sulawesi.
P. nora Felder, 1860

(Common Lineblue — Pl. 8, fig. 6)
Range (1+2+4+5+6+7).–– Sri Lanka, India, Burma, Taiwan, Malay Peninsula,
Sumatra, Java, Lesser Sunda Islands (Takanami, 1986a), Borneo, Palawan, Philippines,
Sulawesi Region, Maluku, New Guinea region, Solomon Islands, northern Australia.
Foodplants.–– Combretaceae (Wynter Blyth, 1982); Acacia, Mimosa, Pithecellobium
(Fabaceae); Myrtaceae; Allophylus (Sapindaceae).
–– P. nora nora Felder, 1860
Range.–– Sulawesi (N, C, S), Kep. Sangihe, Kep. Talaud, Kep. Banggai (Peleng),
Kep. Sula (Sanana, Mangole), C Maluku, New Guinea, Bismarcks.
P. pia Toxopeus, 1929

(Margined Lineblue)
Range (4+6+7).–– India, Nepal, Assam, Burma, Indo-China, Thailand, Malay
Peninsula, Sumatra, Java, Borneo, Sulawesi, C Maluku (Seram).
–– *P. pia elioti Tite, 1963
*P. ella Toxopeus, 1930

Range (E).–– Sulawesi (N, C). Cassidy (1990) records a male from Dumoga-Bone
National Park.
P. gracilis Röber, 1886

Range (1+2+3+4+6+7).–– India, Burma, Thailand, Malay Peninsula, Sumatra, Java,
Borneo, Palawan, Philippines (Luzon, Mindanao: Treadaway, 1995), Sulawesi, N & C
Maluku, New Guinea region.
–– P. gracilis gracilis Röber, 1886.
Range.–– Sulawesi (N, C: Cassidy, 1990), northern and central Maluku (Obi,
Seram), New Guinea region.
P. dubiosa Semper, 1879

(Small Purple Lineblue, or Tailless Lineblue)
Range (1+2+5+6+7).–– Widespread in Oriental and Australian Regions, from Sri
Lanka to Queensland and Solomon Islands, including Palawan and the Philippines
proper (Treadaway, 1995). Presence in Maluku uncertain.
Foodplants.–– Acacia, Archidendron, Cajanus, Dalbergia (Fabaceae); Macadamia (Pro-
teaceae); Litchi (Sapindaceae); attended by ants (e.g. Anoplolepis) on a weak or casual
basis (Cassidy, 1990; Fiedler, 1996b; Braby, 2000). Igarashi & Fukuda (1997) illustrate
larva and pupa.
–– *P. dubiosa subardates Piepers & Snellen, 1918
Range.–– Sulawesi (Takanami, 1987; Cassidy, 1990), Kep. Sangihe, Kep. Talaud,
Tanahjampea, Kalao (Cassidy, 1990).
Nothodanis Hirowatari, 1992

(Pl. 8, fig. 13)
Range (1+2+3+7).–– A recently erected monobasic genus occurring from Indo-

China, north Borneo, Palawan, Philippines, Sulawesi Region, N Maluku, New Guinea
region to the Solomon Islands, Vanuatu and New Caledonia. Previously included in
Danis Fabricius, 1807.
Foodplants.–– Connaraceae (Connarus).
Key works.–– d’Abrera (1977), Hirowatari (1992).
N. schaeffera Erschoff, 1821

(Pl. 8, fig. 13)
–– N. schaeffera schaeffera Erschoff, 1821
Range.–– Northern Borneo, Palawan, Philippines, Kep. Talaud, Sulawesi, Kep.
Togian (Seki et al., 1991).
Catopyrops Toxopeus, 1929

Range (1+2+4+5+6+7).–– Oriental and Australian Regions, from India to the Solo-
mon Islands. Eight species, two of which occur in Sulawesi.
Foodplants.–– Euphorbiaceae, Fabaceae, Sapindaceae (Alectryon, Cupaniopsis),
Ulmaceae (Trema), Urticaceae; attended by ants.
(1981), Parsons (1986), Hirowatari (1992).
C. ancyra Felder, 1860

(Felder’s Lineblue — Pl. 8, fig. 8)
Range (1+2+4+5+6+7).–– Assam, Burma, Thailand, Malay Peninsula, Sumatra,
Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region, C Malu-
ku (Ambon, ?Seram), New Guinea region, Torres Strait, Solomon Islands, Fiji (Hiro-
watari, 1992).
Foodplants.–– Glochidion (Euphorbiaceae); Caesalpinia (Fabaceae); Pipturus (Urti-
caceae) (Parsons 1991; Braby, 2000).
–– *C. ancyra subfestivus Röber, 1886
Range.–– Sulawesi (N, C, S), Kep. Talaud, Kep. Sangihe (Sangihe, Siao), Kep. Tuk-
angbesi, Kep. Banggai (Peleng; Nieuwenhuis, 1946), Kep. Sula (Mangole, Sanana).
C. rita Grose Smith, 1895

Range (5+6).–– Java, Lesser Sunda Islands, Sulawesi (S), Tanahjampea.
–– *C. rita bora Eliot, 1956
Range.–– Sulawesi (C, S: Cassidy, 1990).
–– C. rita altijavana Toxopeus, 1930
Range.–– Java, Tanahjampea.
Ionolyce Toxopeus, 1929

Range (1+2+4+5+6+7).–– Oriental and Australian Regions, from Sri Lanka to Solo-
mon Islands and Vanuatu. Three species, two of which are restricted to the Solomon
Islands and Bougainville.
(1981), Hirowatari (1992), Tennent (2002), Parsons (1999).
I. helicon Felder, 1860

(Pointed Lineblue — Pl. 8, fig. 7)
Range (1+2+4+5+6+7).–– Sri Lanka to Australia and New Guinea region, inclu-
ding Palawan and the Philippines.
–– *I. helicon helicon Felder, 1860
Range.–– Sulawesi (N, C, S), Kep. Talaud, Kep. Banggai (Peleng), Kep. Sula (Sana-
na), C Maluku.
Caleta Fruhstorfer, 1922

(pierrots — Pl. 8, figs 10, 11)
Range (1+2+4+5+6+7).–– Oriental Region, C. Maluku, eastwards to New Guinea.

Three of the nine species occur on Sulawesi.
Foodplants.–– Rhamnaceae; not attended by ants (Fiedler, 1994b, 1996b).
Key works.–– d’Abrera (1977, 1986), Corbet & Pendlebury (1992), Takanami
(1989), Hirowatari (1992).
C. caleta Hewitson, 1876

(Angled Pierrot — Pl. 8, figs 10, 11)
Range (2).–– Southern Philippines (including Sulu Archipelago: Treadaway, 1995),
Sulawesi, Kep. Banggai.
Note.–– Hirowatari (1992) considers argola Hewitson, from southern Philippines,
to be a distinct but sister species of caleta, but Treadaway (1995) continues to treat arg-
ola as a subspecies.
Foodplants.–– Ziziphus (Rhamnaceae).
–– *C. caleta caleta Hewitson, 1876
–– *C. caleta kalawara Ribbe, 1926
Note.–– Takanami (1989) suggests that this taxon is probably a synonym of caleta
caleta.
–– *C. caleta subsp. (Detani, 1983)
C. rhode Hopffer, 1874

Range (4+5).–– Lesser Sunda Islands, Sulawesi Region, Maluku (Buru).
–– *C. rhode rhode Hopffer, 1874
Range.–– Sulawesi (N, C), Kep. Banggai (Peleng; Nieuwenhuis, 1946).

–– *C. rhode rhodana Fruhstorfer, 1918
Range.–– Sulawesi (S), Kalao, Kep. Sula (Sula Mangole).
–– *C. rhode subsp. (BMNH)
*C. celebensis Staudinger, 1889.

Discolampa Toxopeus, 1929

(pierrots — Pl. 8, fig. 9)
Range (W).–– Oriental, extending to the Papuan Region. A small genus of three
species (Hirowatari, 1992), two occurring on Sulawesi.
Foodplants.–– Rhamnaceae; attended by ants (Fiedler, 1996b).
Key works.–– d’Abrera (1977, 1986), Corbet & Pendlebury (1992), Hirowatari (1992).
D. ethion Westwood, 1851

(Banded Blue Pierrot)
Range (W).–– Sri Lanka, India, Burma, Indo-China, south China, Thailand, Malay
wesi, Maluku (no details; Hirowatari, 1992).
Foodplants.–– Ziziphus (Rhamnaceae). Koiwaya & Wakahara (1999) illustrate the
pupa.
–– *D. ethion ulyssides Grose Smith, 1895
D. ilissus Felder, 1859

(Pl. 8, fig. 9)
Range (3+4).–– Sulawesi, Kep. Banggai, northern and central Maluku (Buru).
–– *D. ilissus ilissus Felder, 1859
Jamides Hübner, 1819

(caeruleans — Pl. 8, fig. 14)
Range (W).–– Oriental, Australian and Pacific Regions. An extensive genus of

some 60 species (Hirowatari, 1992, lists 57). About 20 members of this beautiful but
complex group are found in the Sulawesi Region; others may await discovery.
Foodplants.–– Euphorbiaceae, Fabaceae, Marantaceae, Meliaceae, Myrtaceae,
Rutaceae, Sapindaceae, Sterculiaceae, Zingiberaceae; facultatively attended by ants
(Seufert & Fiedler, 1996b).
Key works.–– Riley & Corbet (1938), Corbet & Pendlebury (1992), Common &
Waterhouse (1981), Hirowatari (1986a, 1992), Takanami (1989), Hirowatari & Cassidy
(1994).
J. bochus Stoll, 1782

(Dark Caerulean)
Range (W).–– Widespread in Oriental, Australian and Pacific Regions from Sri
Lanka to Fiji, including Lesser Sunda Islands, Palawan, Philippines, N & C Maluku
and New Guinea region (Parsons, 1999), but not found in Australia.
Foodplants.–– Butea, Caesalpinia, Cajanus, Canavalia, Crotalaria, Derris, Flemingia,
Millettia, Phaseolus, Pongamia, Pueraria, Tephrosia, Vigna, Xylia (Fabaceae); Citrus
(Rutaceae). Igarashi & Fukuda (1997) illustrate all life stages.
–– *J. bochus phaidon Fruhstorfer, 1915
Range.–– Sulawesi, Kep. Talaud, Kep. Banggai (Peleng).
J. seminiger Grose Smith, 1895

Range (P).–– N Maluku, Kep. Sula.
–– *J. seminiger tiglath Fruhstorfer, 1915
*J. biru Ribbe, 1926

Range (L).–– Kep. Banggai.
Note.–– This species is not listed by Hirowatari (1992).
J. cyta Boisduval, 1832

(Pale Caerulean)
Range (1+2+3+5+6+7).–– Burma, Thailand, Malay Peninsula, Sumatra, Java, Lesser
Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region, N Maluku, New Gui-
nea region, northern Australia.
Foodplants.–– Eugenia (Kirton & Kirton, 1987); Syzygium (Braby, 2000) (Myrtace-
ae); Elettaria, Kaempferia (Zingiberaceae).
–– *J. cyta zelia Fruhstorfer, 1916
Range.–– Sulawesi (S), Kep. Banggai (Peleng).
–– J. cyta hellada Fruhstorfer, 1916
*J. snelleni Röber, 1886 (= ohtai Hayashi)

(Snellen’s Caerulean)
J. celeno Cramer, 1775

(Common Caerulean)
Range (W).–– Widespread in Oriental and Australian Regions, from Sri Lanka to
Vanuatu, including Lesser Sunda Islands, Palawan, Philippines, N & C Maluku, New
Guinea region, Solomon Islands, Vanuatu, but not found in Australia.
Foodplants.–– Abrus, Butea, Calopogonium, Canavalia, Delonix, Derris, Dolichos,
Dysolobium, Mucuna, Pongamia, Pueraria, Saraca, Vigna, Xylia (Fabaceae); Donax (Mar-
antaceae); Heynea, Melia, Trichilia (Meliaceae); Theobroma (Sterculiaceae); Elettaria (Zin-
giberaceae); attended by various ant genera (Seufert & Fiedler, 1996b). The early sta-
ges are illustrated by Igarashi & Fukuda (2000).
–– J. celeno optimus Röber, 1886

Range.–– Philippines, Kep. Talaud, Sulawesi, Kep. Tukangbesi, Kep. Banggai
(Peleng).
–– *J. celeno kalawarus Ribbe, 1926
Range.–– Sulawesi (C: Palu district: see Takanami, 1989).
–– *J. celeno subsp. (BMNH)
*J. tsukadai Takanami, 1994

*J. fractilinea Tite, 1960

Range (R).–– Sulawesi, Kep. Sula (Mangole).
J. aratus Stoll, 1781

(Pl. 8, fig. 14)
Range (1+3+4+5+6+7).–– Malay Peninsula, Sumatra, Java, Lesser Sunda Islands,
Borneo, Sibutu (Treadaway, 1995), Palawan, Balabac, Sulawesi Region, N & C Malu-
ku.
Note.–– See Hirowatari (1992) regarding separation of aratus from the more eas-
tern aetherialis Butler.
–– *J. aratus lunata de Nicéville, 1899
Range.–– Sulawesi, Kep. Sangihe, Kep. Banggai (Peleng).
–– *J. aratus makitai Takanami, 1987
–– *J. aratus subsp. (BMNH)
–– *J. aratus djampeana Snellen, 1890
–– *J. aratus subsp. (BMNH)
Range.–– Kep. Tukangbesi (Kaledupa, Binongko).
–– *J. aratus minthe Fruhstorfer, 1916
J. cleodus Felder & Felder, 1865

Range (1+2+7).–– Northern Borneo, Palawan, Philippines, Sulawesi Region.
Note.–– Seki et al. (1991) and Hirowatari (1992) do not record this species for Sula-
wesi or Borneo.
–– *J. cleodus subsp. (= lydanus Fruhstorfer, 1916: homonym)
Range.–– Sulawesi (N), Kep. Banggai (Peleng; Nieuwenhuis, 1946).
J. philatus Snellen, 1878

(Burmese Caerulean)
Range (1+2+3+4+6+7).–– India (Hirowatari, 1992), Burma, Thailand, Malay Penin-
sula, Sumatra, Java, Borneo, Palawan, Philippines, Sulawesi Region, N & C Maluku,
New Guinea.
–– *J. philatus philatus Snellen, 1878

Range.–– Sulawesi, Kep. Banggai (Peleng), Kep. Sula (Sanana).
*J. elioti Hirowatari & Cassidy, 1994

(Eliot’s Caerulean)
*J. festivus Röber, 1886

–– *J. festivus festivus Röber, 1886
–– *J. festivus bangkaia Ribbe, 1926
J. alecto Felder, 1860

(Metallic Caerulean)
Range (W).–– Sri Lanka, India, south China, Taiwan, Indo-China (Hirowatari, 1992),
Sulawesi Region, N & C Maluku, New Guinea (Waigeo, Irian Jaya: BMNH).
Foodplants.–– Hevea (Euphorbiaceae); Pueraria (Fabaceae); Alpinia, Boesenbergia,
Curcuma, Elettaria, Hedychium, Kaempferia, Zingiber (Zingiberaceae). Larvae facultative-
ly attended by a variety of ant genera (Pheidole, Crematohgaster, Tetramorium, Rhoptro-
myrmex, Myrmicaria, Tapinoma, Technomyrmex, Anoplolepis and more). Igarashi & Fuku-
da (1997) illustrate all life stages.
–– *J. alecto subsp. (BMNH)
–– *J. alecto luniger Toxopeus, 1930
–– *J. alecto latimargus Snellen, 1878
Note.–– Hirowatari (1992) lists latimargus (currently ambiguous) as a distinct spe-
cies, endemic to Sulawesi, but also lists the widespread alecto as present on the island.
–– *J. alecto alvenus Fruhstorfer, 1916
*J. halus Takanami, 1994

J. pseudosias Rothschild, 1915

Range (3).–– ?Borneo (Parsons, 1999; not listed by Seki et al., 1991, or Hirowatari,
1992), Sulawesi, N Maluku (including Obi), New Guinea region including New Ire-
land.
–– *J. pseudosias echeilea Fruhstorfer, 1916
*J. species (BMNH)

Range (L).–– Kep. Sula.
Note.–– The identity of this material is uncertain.
J. schatzi Röber, 1886

Range (1+2+3).–– Palawan, Philippines (Treadaway, 1995), Sulawesi Region, N
Maluku (including Obi).
–– *J. s. argentiferus Fruhstorfer, 1916
Range.–– Sulawesi (N), Kep. Banggai (Peleng: Detani, 1983).
–– *J. s. demetrias Fruhstorfer, 1916
Range.–– Kep. Talaud, Kep. Sangihe (Sangihe, Siao), ?Kep. Sula.
J. elpis Godart, 1824

Range (W).–– Sikkim, Assam, Malay Peninsula, Sumatra, Java, Borneo, Palawan,
Philippines, Sulawesi Region, N & C Maluku, Timor.
Note.–– J. elpis is not listed by Seki et al. (1991) for Sulawesi Region or Maluku.
Foodplants.–– Sapindaceae (Lepisanthes: Fiedler, unpubl., in West Malaysia); Boe-
senbergia, Elettaria (Zingiberaceae).
–– *J. elpis espada Fruhstorfer, 1916
–– *J. elpis comeda Fruhstorfer, 1916
*J. celebica Eliot, 1969

Catochrysops Boisduval, 1832

(forget-me-nots — Pl. 8, fig. 15)
Range (W).–– Sri Lanka, India, and through the Malay Archipelago (including
Lesser Sunda Islands, Borneo, Philippines and Maluku) to Australia, New Caledonia
and Society Islands. A genus of six species, well represented on Sulawesi.
Foodplants.–– Fabaceae, Sapindaceae; attended by ants.
(1981), Hirowatari (1992).
C. strabo Fabricius, 1793

(Forget-me-not)
Range (W).–– Oriental and Australian Regions from Sri Lanka to Louisiade Archi-
pelago, including Lesser Sunda Islands, Palawan, Philippines and N & C Maluku.
Foodplants.–– Abrus, Acacia, Butea, Cajanus, Cylista, Desmodium, Dolichos, Dunbaria,
Lablab, Phaseolus, Phyllodium, Pisum, Vigna (Fabaceae); Schleichera (Wynter Blyth, 1982)
(Sapindaceae).
–– C. strabo celebensis Tite, 1959
Range.–– Sulawesi, Kep. Tukangbesi, Kalao, Buton, Kep. Sula, Maluku.
–– C. strabo luzonensis Tite, 1959
Range.–– Palawan, Philippines, Kep. Talaud, Kep. Sangihe.
C. strabobinna Swinhoe, 1916

(Pl. 8, fig. 15)
Range (3+4+5).–– Lesser Sunda Islands (including Bali), Sulawesi, Kep. Talaud,
Kep. Tukangbesi, Kep. Sula (Sula Mangole), N & C Maluku.
Note.–– Hirowatari (1992) gives only Maluku.
C. panormus Felder, 1860

(Silver Forget-me-not)
Range (W).–– As genus (limited known range in Philippines: see Treadaway,
1995).
Foodplants.–– Caesalpinia, Cajanus, Crotalaria, Dendrolobium, Dolichos, Flemingia, Phaseo-
lus (Fabaceae).
–– *C. panormus subsp. (BMNH)
Lampides Hübner, 1819

(peablues — Pl. 8, fig. 16)
Range (W).–– A monobasic genus distributed throughout Africa and the Indo-
Australian Region, and extending to southern Europe and Hawaii.
Foodplants.–– Mainly buds and pods of many legumes (Fabaceae), including Butea,
Cajanus, Canavalia, Chamaecytisus, Clianthus, Crotalaria, Cullen, Dolichos, Dunbaria, Gly-
cine, Gompholobium, Kennedia, Lablab, Lathyrus, Lespedeza, Lotus, Lupinus, Medicago,
Melilotus, Millettia, Phaseolus, Pisum, Psophocarpus, Psoralea, Pueraria, Pultenaea, Sesba-
nia, Swainsona, Vicia, Vigna, Virgilia; additionally on Tecoma (Pelzer, 1991) (Bignoniace-
ae); Capparis (Jordano et al., 1988 in Spain, during drought) (Capparidaceae); Macaran-
ga (Euphorbiaceae) and Lilium (Liliaceae); attended facultatively by a variety of ants
(Fiedler, in Hesselbarth et al., 1995).
Key works.–– Corbet & Pendlebury (1992), Common & Waterhouse (1981), Hiro-
watari (1992).
L. boeticus Linnaeus, 1767

(Long-tailed Blue, or Peablue — Pl. 8, fig. 16)
Range (W).–– As genus, including Lesser Sunda Islands, Borneo, Palawan, Philip-
pines, Sulawesi, Kep. Talaud, Kep. Banggai (Peleng), Galla and N & C Maluku.
Castalius Hübner, 1819

(Pl. 8, figs 18, 19)
Range (2+5+6+7).–– Sri Lanka, India, southern China, Indo-China, Malay Peninsu-
la, Sumatra, Java, Lesser Sunda Islands, Borneo, Philippines (Luzon, Samar: Treada-
way, 1995), Sulawesi Region. Four species, all of which occur on Sulawesi.
Note.–– Takanami (1989) places these species in the genus Tarucus Moore, 1881,
otherwise known from the Afrotropical Region and the Indian subregion, but Evans
(1955) specifically excluded the Sulawesi Region species; Larsen (1982) regards Castalius
(type species: Papilio rosimon Fabricius) as strictly monobasic; Hirowatari (pers. comm.
to J. N. Eliot) considers that the three additional Sulawesi taxa listed here belong to Cas-
talius, but Hirowatari (1992) gives only two species for the genus, rosimon and fasciatus.
Thus, the species clathratus and fluvialis may be newly combined here in Castalius, and it
is clear that this group is in need of formal revision.
Foodplants.–– Rhamnaceae.
Key works.–– Larsen (1982), Corbet & Pendlebury (1992), Hirowatari (1992).
C. rosimon Fabricius, 1775

(Common Pierrot)
Range (2+5+6+7).–– As genus, except restricted to Sulawesi in Sulawesi Region.
Foodplants.–– Paliurus (Bascombe et al., 1999), Ziziphus (Rhamnaceae). Igarashi &
Fukuda (2000) illustrate the foodplant and early stages.
–– *C. rosimon silas Fruhstorfer, 1922
*C. fasciatus Röber, 1887

(Pl. 8, figs 18, 19)
–– *C. fasciatus adorabilis Fruhstorfer, 1918
–– *C. fasciatus fasciatus Röber, 1887
*C. clathratus Holland, 1891

*C. fluvialis Grose Smith, 1895

Famegana Eliot, 1973

(grass blues — Pl. 8, fig. 22)
Range (5).–– Southern China, Hainan, Taiwan, Lesser Sunda Islands, Philippines
(Luzon: Treadaway, 1995), Sulawesi, New Guinea region, Vanuatu, Fiji, Samoa,
Tonga, Australia (monobasic).
Foodplants.–– Buds and flowers of Fabaceae; Zygophyllaceae; attended by ants.
Key works.–– Common & Waterhouse (1981), Hirowatari (1992), Parsons (1999).
F. alsulus Herrich-Schäffer, 1869

(Black-spotted Grass Blue — Pl. 8, fig. 22)
Range (5).–– As genus.
Foodplants.–– Cajanus, Desmodium, Flemingia, Indigofera, Moghamia, Phyllodium
(Fabaceae); additionally recorded from Zygophyllaceae (Shen-Horn Yen in litt., from
Taiwan).
–– *F. alsulus kalawarus Ribbe, 1926

Pithecops Horsfield, 1828

(quakers — Pl. 8, fig. 25)
Range (W).–– Oriental Region to New Guinea region, Solomon Islands and nort-
hern tip of Cape York. A small genus of five species (Hirowatari, 1992), two of which
occur in the Sulawesi Region.
Foodplants.–– Fabaceae, Rubiaceae, Rutaceae.
Key works.–– Cowan (1966a), Corbet & Pendlebury (1992), Hirowatari (1992).
P. corvus Fruhstorfer, 1919

(Forest Quaker)
Range (P).–– India, Burma (Hirowatari, 1992), Indo-China, Taiwan, Ryukyu
Islands, Thailand, Malay Peninsula, Sumatra, Java, western Lesser Sunda Islands, Bor-
neo, Palawan, Philippines, Kep. Talaud.
Foodplants.–– Desmodium (Fabaceae); Gardenia (Rubiaceae); Glycosmis (Rutaceae).
Igarashi & Fukuda (2000) illustrate one of the foodplants and the early stages.
–– P. corvus corax Fruhstorfer, 1917
Range.–– Java, western Lesser Sunda Islands, Borneo, Philippines, Kep. Talaud.
Note.–– Seki et al. (1991) treat corax as a synonym of corvus corvus.
*P. phoenix Röber, 1886

(Sulawesi Quaker — Pl. 8, fig. 25)
Range (R).–– Sulawesi, Kep. Talaud, Kep. Sangihe, Kep. Banggai (Peleng), Kep.
Sula (Mangole, Sanana).
Note.–– Takanami (1989) considers moeros Staudinger, 1888, from northern Sula-
wesi to be a good subspecies of P. phoenix.
Leptotes Scudder, 1876 (= Syntarucus Butler, 1900)

(zebra blues — Pl. 8, fig. 17)
Range (2+3+4+5+6+7).–– Palaearctic, Afrotropical, Oriental and Australian Regions.

Best developed in Africa, the genus is only represented in the Indo-Australian region
by a single polytypic species (not so far recorded from Malay Penisnula or Palawan:
Corbet & Pendlebury, 1992; Treadaway, 1995).
Foodplants.–– Fabaceae, Fagaceae, Plumbaginaceae, Rhamnaceae, Rosaceae; atten-
ded by ants (Fiedler, in Hesselbarth et al., 1995).
Key works.–– Common & Waterhouse (1981), Corbet & Pendlebury (1992).
L. plinius Fabricius, 1793

(Zebra Blue, Plumbago Blue — Pl. 8, fig. 17)
Range (2+3+4+5+6+7).–– Sri Lanka, India, Indo-China, Sumatra, Java, Lesser Sunda
Islands, Taiwan, Borneo (one male: Seki et al., 1991), Philippines (Luzon, Leyte, Mind-
anao: Treadaway, 1995), Sulawesi Region, N & C Maluku, New Guinea region, Austra-
lia, Vanuatu, New Caledonia.
Foodplants.–– Albizia, Dolichos, Galactia, Galscutia, Glycine, Indigofera, Lablab, Mimo-

sa, Rhynchosia, Sesbania, Tephrosia (Fabaceae); Dyerophytum, Plumbago (Plumbaginace-
ae); Ziziphus (Rhamnaceae); sometimes attended by ants. Igarashi & Fukuda (1997)
illustrate all life stages.
–– *L. plinius plutarchus Fruhstorfer, 1922
Range.–– Sulawesi (N, S), Kep. Talaud, Kep. Sangihe, Kep. Sula (Mangole).
–– *L. plinius celis Fruhstorfer, 1922
–– *L. plinius zingis Fruhstorfer, 1922
Range.–– Buton.
Zizeeria Chapman, 1910

(grass blues — Pl. 8, fig. 20)
Range (W).–– Palaeotropics, southern and eastern Palaearctic. A genus of two allo-
patric species.
Foodplants.–– Aizoaceae, Amaranthaceae, Chenopodiaceae, Euphorbiaceae, Fabace-
ae, Molluginaceae, Oxalidaceae, Polygonaceae, Zygophyllaceae; attended by ants (Fied-
ler & Hagemann, 1995).
Z. karsandra Moore, 1865

(Dark Grass Blue — Pl. 8, fig. 20)
Range (W).–– From Algeria and northern Arabia, eastwards throughout the Orien-
tal Region to Australia, including the Lesser Sunda Islands, Palawan, Philippines,
Moluccas (Seki et al., 1991), New Guinea (Parsons, 1999).
Foodplants.–– Glinus (Aizoaceae); Amaranthus (Amaranthaceae); Glycine, Medicago,
Zornia (Fabaceae); Oxalis (Oxalidaceae); Polygonaceae; Tribulus (Zygophyllaceae);
associated facultatively with ants (Tapinoma: Fiedler, in Hesselbarth et al., 1995).
–– Z. karsandra karsandra Moore, 1865
Range.–– As for species, including Lesser Sunda Islands, Sulawesi (S), Kep. Tuk-
angbesi and Maluku (no details), but not Australia.
Zizina Chapman, 1910

(lesser grass blues — Pl. 8, fig. 21)
Range (W).–– Palaeotropics. Three allopatric species, one confined to Africa and
peninsular India, and another to the Australian Region and the Pacific.
Foodplants.–– Fabaceae, Zygophyllaceae; attended by ants.
Z. otis Fabricius, 1787

(Lesser Grass Blue — Pl. 8, fig. 21)
Range (W).–– Indo-China to Japan, Malay Peninsula, Sumatra, Java, Lesser Sunda
Islands (Takanami, 1986a), Borneo, Palawan, Philippines, Sulawesi Region, N & C
Maluku.
Foodplants.–– Alysicarpus, Cullen, Daviesea, Desmodium, Hardenbergia, Indigofera,

Lotus, Mimosa, Pultenaea, Sesbania, Swainsona, Trifolium, Trigonella, Vandellia, Vigna,
Zornia (Fabaceae); in Australia also on a number of introduced Fabaceae including:
Glycine, Lupinus, Macroptilium, Medicago, Phaseolus, Pisum, Trifolium, Vicia, Virgilia
(Braby, 2000); Tribulus (Zygophyllaceae).
–– *Z. otis subsp. (BMNH)
Range.–– Sulawesi, Salayar.
–– *Z. otis subsp. (Detani, 1983)
–– Z. otis tanagra Felder, 1860
Range.–– Kep. Tukangbesi, Kep. Sula (Sanana), N & C Maluku.
Zizula Chapman, 1910

(tiny grass blues — Pl. 8, fig. 23)
Range (W).–– Pantropical. Two allopatric species, one confined to the Americas.
Foodplants.–– Acanthaceae, Fabaceae, Oxalidaceae, Verbenaceae, Zygophyllaceae;
attended by ants.
Z. hylax Fabricius, 1775

(Tiny Grass Blue — Pl. 8, fig. 23)
Range (W).–– Afrotropical, Oriental and Australian Regions, including Malay
wesi Region, Maluku, New Guinea region, Solomon Islands, Vanuatu, New Caledo-
nia.
Note.–– Larsen (in press) is of the view that division of hylax into subspecies is not
really practicable.
Foodplants.–– Belopeone, Dicliptera, Dipteracanthus, Blechum, Hygrophila, Nelsonia,
Phaulopsis, Ruellia (Australia, introduced; Braby 2000), Strobilanthes (Acanthaceae; other
genera in Africa); Desmodium, Mimosa, Vicia (Fabaceae); Oxalis (Oxalidaceae); Lantana
(Verbenaceae); Zygophyllaceae. Igarashi & Fukuda (2000) illustrate the larva and pupa.
–– Z. hylax hylax Fabricius, 1775
Range.–– Sri Lanka, India, Indo-China, Malay Peninsula, Sumatra, Java, Lesser
Sunda Islands, Borneo, Palawan, Philippines, Sulawesi, Kep. Talaud, Kep. Tukangbe-
si, Kep. Banggai (Peleng), Kep. Sula (Sanana), N & C Maluku, New Guinea, Guam,
Fiji, Loyalty Islands.
Everes Hübner, 1819

(cupids, tailed or short-tailed blues — Pl. 8, fig. 24)
Range (W).–– Primarily found in the Holarctic and Sino-Himalayan regions, with
about half a dozen species; one member extends throughout the Oriental Region east
to Australia.
Foodplants.–– Crassulaceae, Fabaceae, Gesneriaceae. Facultatively attended by ants.
E. lacturnus Godart, 1824

(Tailed Cupid — Pl. 8, fig. 24)
Range (W).–– Oriental Region east to Australia and the Solomon Islands, inclu-
ding Malay Peninsula, Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philip-
pines and N & C Maluku.
Foodplants.–– Desmodium, Lotus, Trifolium (Fabaceae); Lysionotus (Gesneriaceae)
(Shen-Horn Yen in litt., from Taiwan).
–– *E. lacturnus subsp. (BMNH)
Range.–– Kep. Talaud, Kep. Sangihe.
–– *E. lacturnus subsp. (Detani, 1983)
Range.–– Kep. Sula (Sula Mangole).
Neopithecops Distant, 1884

(quakers — not illustrated)
Range (P).–– Sri Lanka to Taiwan, Malay Peninsula, Greater and Lesser Sunda
Islands, Palawan, Philippines, Kep. Sula, northern Maluku (including Obi) and New
Guinea region, just reaching northern Australia, but not recorded from Sulawesi. A
small genus of five known species.
Foodplants.–– Ebenaceae (Diospyros); Rutaceae (Glycosmis); sometimes attended
by ants.
Key works.–– Eliot & Kawazoé (1983), Cassidy (1995b).
N. sumbanus Eliot & Kawazoé, 1983

Range (P).–– Lesser Sunda Islands, Tanahjampea.
–– N. sumbanus sumbanus Eliot & Kawazoé, 1983
Range.–– Sumba, Tanahjampea.
N. umbretta Grose Smith, 1895

Range (P).–– Lesser Sunda Islands, Tanahjampea, Kep. Sula, N Maluku.
–– *N. umbretta tituria Fruhstorfer, 1919
Range.–– Lesser Sunda Islands, Tanahjampea (Takanami, 1986a).
–– *N. umbretta dorothea Eliot & Kawazoé, 1983
Megisba Moore, 1881

(malayans — Pl. 8, fig. 26)
Range (W).–– Oriental and Australian Regions. Two allopatric species.

Foodplants.–– Euphorbiaceae, Rhamnaceae, Sapindaceae.
Key works.–– Common & Waterhouse (1981), Eliot & Kawazoé (1983), Corbet &
Pendlebury (1992), Cassidy (1995b).
M. malaya Horsfield, 1828

(Malayan — Pl. 8, fig. 26)
Range (1+2+5+6+7).–– Sri Lanka to Indo-China, Malay Peninsula, Sumatra, Java,
Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region.
Foodplants.–– Macaranga, Mallotus, Trigonostemon (Euphorbiaceae); Rhamnus
(Rhamnaceae); Allophylus, Schmidella (Sapindaceae).
–– M. malaya sikkima Moore, 1884
Range.–– Northern India to Taiwan and Ryukyu Islands, Malay Peninsula, Suma-
tra, Java, Borneo, Palawan, Philippines, Sulawesi (N, C, S), Kep. Sangihe, Kep. Tuk-
angbesi, Kep. Banggai (Peleng), Kep. Sula.
Cebrella Eliot & Kawazoé, 1983

(hedge blues — not illustrated)
Range (2+6+7).–– Malay Peninsula, Bangka, Sumatra, Java, Borneo, Philippines

(Mindanao, Panay) and Sulawesi. Six species divided into two subgenera; the subge-
nus found on Sulawesi has four members. C. (Chelakina) matanga Chapman, or a very
closely related species, has been bred in Borneo from an aquatic larva found in pitcher
plants (J. N. Eliot, pers. comm.).
Key works.–– Eliot & Kawazoé (1983).
Cebrella (Chelakina) Eliot & Kawazoé, 1983
Range.–– Bangka, Borneo and Sulawesi. Three described species are known from
Borneo, one of which also occurs on Bangka; the Sulawesi species has yet to be descri-
bed (and is not discussed by Cassidy, 1995b).
*C. species nova (Eliot in litt.)

Sancterila Eliot & Kawazoé, 1983

(Pl. 8, fig. 27)
Range (4).–– Sulawesi and central Maluku. Four species, three of which occur on
Sulawesi; the fourth is known from Buru and Ambon.
*S. deliciosa Pagenstecher, 1896

(Pl. 8, fig. 27)
–– *S. deliciosa deliciosa Pagenstecher, 1896
–– *S. deliciosa sohmai Eliot & Kawazoé, 1983
Range.–– Sulawesi (C: Cassidy, 1995b).
*S. russelli Eliot & Kawazoé, 1983

*S. drakei Cassidy, 1995

Udara Toxopeus, 1928

(hedge blues — Pl. 8, fig. 28)
Range (W).–– Oriental and Australian Regions (including Australia), just exten-
ding into the eastern Palaearctic, and to Hawaii. About 40 species (Parsons, 1999),
divided amongst three subgenera, one with eight species restricted to New Guinea,
another monobasic and restricted to Hawaii.
Foodplants.–– Aquifoliaceae, Caprifoliaceae, Fabaceae, Fagaceae, Rosaceae, Rubiace-
ae, Sapindaceae, Symplocaceae, Urticaceae.
Key works.–– d’Abrera (1977), Eliot & Kawazoé (1983), Corbet & Pendlebury
(1992), Cassidy (1995b).
Udara (Udara) Toxopeus, 1928
Range.–– As genus, except Hawaii. About 20 species, six of which occur on Sula-
wesi.
U. dilecta Moore, 1879

(Pale Hedge Blue)
Range (2+4+5+6+7).–– Himalayas and Indo-China to Japan, Malay Peninsula,
Sumatra, Java, western Lesser Sunda Islands, Borneo, ?Palawan (not confirmed by
Treadaway, 1995), Philippines, Sulawesi, C Maluku (Buru, Seram), New Guinea.
Foodplants.–– Castanopsis (Fagaceae). Igarashi & Fukuda (2000) illustrate the larva
and pupa.
–– *U. dilecta thoria Fruhstorfer, 1910
U. rona Grose Smith, 1894

Range (4+6).–– Malay Peninsula, Sumatra, Java, Sulawesi, central Maluku, New
Guinea, New Britain.
–– U. rona rona Grose Smith, 1894
Range.–– Sulawesi (N, C), C Maluku, New Guinea and New Britain.
U. placidula H.H. Druce, 1895

Range (W).–– Assam, Indo-China, Malay Peninsula, Sumatra, Java, Lesser Sunda
Islands, Borneo, Palawan, Philippines, Sulawesi, N & C Maluku.
–– U. placidula placidula Druce, 1895
Range.–– Borneo, Sulawesi (N, C).
U. camenae de Nicéville, 1895

(Pl. 8, fig. 28)
Range (2+4+7).–– Malay Peninsula, Sumatra, Borneo, ?Palawan (not confirmed by
Treadaway, 1995), Philippines, Sulawesi, C Maluku.
–– *U. camenae euphon Fruhstorfer, 1910
Range.–– Sulawesi (N, C, S: Cassidy, 1995b).
*U. aristius Fruhstorfer, 1910

–– *U. aristius lewari Ribbe, 1926.
–– *U. aristius aristius Fruhstorfer, 1910
*U. etsuzoi Eliot & Kawazoé, 1983

Sidima Eliot & Kawazoé, 1983

(not illustrated)
Range (2).–– Sumatra, Mindanao, Sulawesi, New Guinea. Four allopatric species.
*S. sulawesiana Eliot & Kawazoé, 1983

Acytolepis Toxopeus, 1927

Range (1+2+5+6+7).–– Oriental Region to southern Japan, Java, Lesser Sunda

Islands, Borneo, Philippines, Sulawesi Region and ?Maluku. Five species, three of
which occur on Sulawesi.
Foodplants.–– Caprifoliaceae, Combretaceae, Cycadaceae, Dipterocarpaceae, Eri-
caceae, Euphorbiaceae, Fabaceae, Fagaceae, Hamamelidaceae, Malphigiaceae, Myri-
caceae, Rosaceae, Sapindaceae, Saxifragaceae, Ulmaceae; sometimes ant attended.
Key works.–– Eliot & Kawazoé (1983), Corbet & Pendlebury (1992), Cassidy
(1995b).
A. puspa Horsfield, 1828

(Common Hedge Blue)
Range (1+2+5+6+7).–– Sri Lanka to Indo-China and Japan, Malay Peninsula,
Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi
Region, ?C Maluku.
Foodplants.–– Viburnum (Caprifoliaceae); Combretaceae; Cycas (Cycadaceae); Sho-
rea (Dipterocarpaceae); Enkianthus, Lyonia, Rhododendron, Vaccinium (Ericaceae); Anti-
desma, Breynia, Bridelia, Glochidion (Euphorbiaceae); Calliandra, Cylista, Paracalyx, Pel-
tophorum, Xylia (Fabaceae); Quercus (Fagaceae); Distylum (Hamamelidaceae); Hiptage

(Malphigiaceae); Myrica (Myricaceae); Aruncus, Chaenomeles, Malus, Photinia, Prunus,
Rosa, Spiraea (Rosaceae; several other genera in Japan); Dimocarpus, Euphoria, Litchi,
Sapindus, Schleichera (Sapindaceae); Astilbe (Saxifragaceae); Celtis (Ulmaceae) (Fukuda
et al., 1992; Fiedler, unpubl.). Facultatively associated with ants (Fiedler, 1996b). Iga-
–– *A. puspa kuehni Röber, 1886
Range.–– Sulawesi (N, C, S, E), Kep. Banggai.
–– *A. puspa deronda Fruhstorfer, 1922
Range.–– ?Tondano (Cassidy, 1995b), Kep. Sula (Mangole, Sanana).
*A. najara Fruhstorfer, 1910

Range (E).–– Sulawesi (N, C, S: Cassidy, 1995b).
*A. samanga Fruhstorfer, 1910

(Pl. 8, fig. 29)
Celastrina Tutt, 1906

(holly blues, hedge blues — Pl. 8, fig. 30)
Range (W).–– Holarctic and Oriental Regions, extending to Papuan Region. About
15 species, one of them (C. argiolus) being extremely widespread; two species occur in
Sulawesi.
Foodplants.–– Aceraceae, Anacardiaceae, Aquifoliaceae, Araliaceae, Asteraceae,
Buddlejaceae,Caprifoliaceae, Celastraceae, Cornaceae, Ericaceae, Fabaceae, Fagaceae,
Hamamelidaceae, Hippocastanaceae, Lamiaceae, Lythraceae, Moraceae, Oleaceae,
Polygonaceae, Ranunculaceae, Rhamnaceae, Rosaceae, Rutaceae, Saxifragaceae, Sta-
phyleaceae, Theaceae, Ulmaceae; sometimes ant-attended.
Key works.–– Eliot & Kawazoé (1983), Corbet & Pendlebury (1992) Cassidy
(1995b)
C. philippina Semper, 1889

(Philippine Hedge Blue — Pl. 8, fig. 30)
Range (1+2+3+4+5+7).–– Borneo, Palawan, Philippines, Sulawesi Region, N & C
Maluku, eastern Lesser Sunda Islands, New Guinea region.
–– *C. philippina gradeniga Fruhstorfer, 1910
Range.–– Sulawesi (N, E, S), Kep. Sula.
–– C. philippina philippina Semper, 1889
Range.–– Borneo, Palawan, Philippines, Kep. Talaud.
C. lavendularis Moore, 1877

(Plain Hedge Blue)
Range (2+3+4+5+6+7).–– Sri Lanka to Indo-China and Taiwan, Malay Peninsula,
Sumatra, Java, Lesser Sunda Islands, Borneo, Philippines (see Treadaway, 1995), Sula-
wesi, N & C Maluku, New Guinea.
Foodplants.–– Millettia (Fabaceae); Acer (Aceraceae); Celtis (Ulmaceae) (last two

records from Shen-Horn Yen, for Taiwan); ant-attended.
–– *C. lavendularis lyce Grose Smith, 1896
*Uranobothria Toxopeus, 1927

Range (E).–– Sulawesi. An endemic genus of two species; according to Eliot &
Kawazoé (1983), possibly related to the monobasic genus Notarthrinus from Assam
and Burma.
*U. celebica Fruhstorfer, 1917

*U. tsukadai Eliot & Kawazoé, 1983

(Tsukada’s Hedge Blue — Pl. 8, fig. 31)
Range (E).–– Sulawesi (N, C: Cassidy, 1995b).
Monodontides Toxopeus, 1927

Range (1+2+3+5+6+7).–– Oriental and Australian Regions (but not Australia, and
not recorded from central Maluku). Two subgenera, one monobasic, the other with
seven species, both represented on Sulawesi.
Key works.–– Eliot & Kawazoé (1983), Corbet & Pendlebury (1992), Cassidy (1995b).
Monodontides (Monodontides) Toxopeus, 1927
Range.–– As genus. Seven species, with one member in Sulawesi.
M. (M.) kolari Ribbe, 1926

(Pl. 8, fig. 32)
Range (2).–– Mindanao, Sulawesi (N, C: Cassidy, 1995b).
*Monodontides (Buakraengius) Eliot & Kawazoé, 1983
Range.–– Sulawesi (monobasic).
*M. (B.) cara de Nicéville, 1898

Euchrysops Butler, 1900

(plain cupids, gram blues — Pl. 8, fig. 33)
Range (1+2+4+5+6+7).–– Richly represented in the Afrotropical Region, but with

only a single species in the Oriental, Australian and Pacific Regions.

Foodplants.–– Boraginaceae, Cycadaceae, Euphorbiaceae, Fabaceae, Lamiacae,
Myrtaceae, Orchidaceae, Scrophulariaceae, Verbenaceae; attended by ants.
E. cnejus Fabricius, 1798

(Gram Blue — Pl. 8, fig. 33)
Range (1+2+4+5+6+7).–– Arabia, Sri Lanka to India and Indo-China, Malay Penin-
sula and Philippines eastwards to C Maluku (Buru) and New Guinea, the Pacific and
Australia. Watson et al. (1995) also record Kenya.
Foodplants.–– Cycas (Cycadaceae); Hevea (Euphorbiaceae); Abrus, Acacia, Butea,
Cajanus, Canavalia, Crotalaria, Desmodium, Flemingia, Lablab, Macroptilium, Paracalyx,
Phaseolus, Pisum, Psophocarpus, Pueraria, Sesbania, Vigna (Fabaceae); Dendrobium (Orchi-
daceae); Clerodendrum (Verbenaceae); attended by ants (Camponotus, Crematogaster, Iri-
domyrmex, Polyrhachis). Watson et al. (1995) describe the life history.
–– *E. cnejus subsp. (BMNH)
Range.–– Sulawesi (N, C, S), Kep. Banggai (Peleng; Nieuwenhuis, 1946), Kep. Sula
(Mangole, Sanana), Kep. Tukangbesi.
–– E. cnejus luzonicus Röber, 1886
Range.–– Philippines (Palawan, Cebu, Leyte, Luzon, Tawitawi), Kep. Sangihe,
Kep. Talaud.
Note.–– Treadaway (1995) includes all Philippine records within the typical sub-
species, E. cnejus cnejus.
Chilades Moore, 1881

(lime blues and grass jewels — Pl. 8, figs 34, 35)
Range (W).–– Palaearctic, Afrotropical, Oriental and Australian Regions, exten-

ding to Lesser Sunda Islands, Philippines, Sulawesi, Maluku, Solomon Islands and
Australia. A genus of approximately 22 species (including two species recently transf-
erred from Freyeria Couvoisier, a junior synonym according to Fiedler (1991) and Hes-
selbarth et al. (1995). Three Chilades are found on Sulawesi.
Foodplants.–– Anacardiaceae, Boraginaceae, Cycadaceae, Euphorbiaceae, Fabace-
ae, Rutaceae, Tiliaceae; some species attended facultatively by ants (e.g. Iridomyrmex:
Fiedler, in Hesselbarth et al., 1995).
Key works.–– d’Abrera (1977, as Luthrodes; 1986), Corbet & Pendlebury (1992).
C. boopis Fruhstorfer, 1915

(Pl. 8, fig. 34)
Range (3+4).–– Sulawesi, N & C Maluku, Misool, Waigeo.
–– *C. boopis boopis Fruhstorfer, 1915
Range.–– Sulawesi (N, C), Kep. Banggai (Peleng).
C. lajus Stoll, 1780

(Lime Blue)
Range (1+2+7).–– Sri Lanka to Indo-China, Taiwan and Japan, Assam, Malay
Peninsula, northern Borneo (Mangalum I.), Palawan, Philippines, Sulawesi.

Note.–– Igarashi & Fukuda (2000: 563) do not include Sulawesi in the distribution
of this species.
Foodplants.–– ?Cycadaceae (probably refers to Chilades pandava); Atalantia, Citrus,
Feronia, Limonia, Naringi, Severinia, Triphasia (Rutaceae); Tilia (Tiliaceae). Larvae occa-
sionally carnivorous on aphids (Agarwala & Saha, 1984). Igarashi & Fukuda (2000)
illustrate the larva and pupa.
–– *C. lajus cromyon Fruhstorfer, 1916
C. putli Kollar, 1848

(Least Grass Jewel — Pl. 8, fig. 35)
Range (5+6).–– Sri Lanka, India, Nepal, southern China, Indo-China, Java, Lesser
Sunda Islands, Sulawesi, New Guinea, Australia.
Note.–– Formerly included in the genus Freyeria, this small species appears to be
absent from the Malay Peninsula, Sumatra, Borneo, Maluku and the Philippines, but
its precise distribution requires confirmation. In the past putli has often been treated
as a subspecies of trochylus Freyer, but more recently (e.g. Fujioka, 1970) many authors
have considered it to be distinct. According to Smith (1994) both species fly in Nepal;
according to Koiwaya (1989: 99) both fly in China; H.S. Rose and A.K. Sidhu (in litt.,
1996) found both in India; Motono & Negishi (1989) list both for Laos, but illustrate
only putli, suggesting that they did not find true trochylus locally. Treadaway (1995)
lists F. trochylus gnoma Snellen from Luzon, but not elsewhere in the Philippines; the
identity should be checked.
Foodplants.–– Heliotropium (Boraginaceae); Alysicarpus, Flemingia, Indigofera, Lotus,
Pisum, Rhynchosia, Zornia (Fabaceae); attended by ants (Iridomyrmex).
Riodinidae Grote, 1895 (1827)

(metalmarks, punches, judies — Pl. 8, figs 36, 37)
Range.–– Cosmopolitan, but the great majority of the ca 1500 species occur in the
neotropics. Five subfamilies currently recognised (but two South American groups are
likely to be downgraded), only one of which occurs outside of the Americas.
Foodplants.–– Myrsinaceae (in Oriental Region); many South American species
are thought to be associated with ants.
Key works.–– d’Abrera (1977, 1986), Harvey (1987).
Nemeobiinae Bates, 1868

(punches, judies)
Range.–– Exclusively Old World, including Palaearctic, Afrotropical, Oriental, and

Indo-Australian regions; of the approximately 100 species, one just reaches the nort-
hern tip of Queensland. About seven genera occur in the Malay Archipelago west of
Maluku, of which two are found in Sulawesi.
Foodplants.–– See family.
Key works.–– Bennett (1950), Harvey (1987), Corbet & Pendlebury (1992).
Zemeros Boisduval, 1836

(punchinellos — Pl. 8, fig. 36)
Range (1+5+6+7).–– Northern India and Indo-China to Lesser Sunda Islands, Pala-
wan and Sulawesi Region. Two species, both of which have been recorded from Sula-
wesi (but one requires confirmation).
Foodplants.–– Myrsinaceae.
Key works.–– d’Abrera (1986), Corbet & Pendlebury (1992).
Z. flegyas Cramer, 1780

(Punchinello — Pl. 8, fig. 36)
Range (1+5+6+7).–– Sikkim, China, Indo-China, Malay Peninsula, Sumatra, Java,
Lesser Sunda Islands, Borneo, Palawan (Treadaway, 1995), Sulawesi Region.
Foodplants.–– Maesa (Myrsinaceae). Igarashi & Fukuda (2000) illustrate foodplant
and early stages.
–– *Z. flegyas celebensis Fruhstorfer, 1899
–– *Z. flegyas sosiphanes Fruhstorfer, 1912
Z. emesoides Felder & Felder, 1860

Range.–– Malay Peninsula, Sumatra, Borneo, ?Banggai, ?Philippines (Sulu Archi-
pelago - not confirmed by Treadaway, 1995), ?Sulawesi.
–– *Z. emesoides subsp. (BMNH)
Note.–– Requires confirmation; Otsuka (1988) confirms only the records for Neo-
malaya.
Abisara Felder & Felder, 1860

(judies — Pl. 8, fig. 37)
Range (1+2+6+7).–– Afrotropical and Oriental Regions, including Wallacea. About a

dozen of the 30 or so species occur in the Malay Peninsula, including two on Sulawesi.
Foodplants.–– Myrsinaceae.
Key works.–– Bennett (1950), d’Abrera (1986), Corbet & Pendlebury (1992).
A. echerius Stoll, 1790

(Plain Judy)
Range (1+2).–– Sri Lanka, India, China, Indo-China, Burma, Ryukyu Islands, Hai-
nan, Palawan, Philippines (Basilan, Sibutu, Bongao, Sanga Sanga, Tawitawi, Panay,
Mindoro, Luzon: Treadaway, 1995), Sulawesi Region.
Foodplants.–– Ardisia, Embelia, Maesa (Myrsinaceae) (Igarashi & Fukuda, 2000,
who also illustrate foodplant and early stages.
–– *A. echerius bugiana Fruhstorfer, 1904
–– *A. echerius celebica Röber, 1886
–– *A. echerius saleyra Fruhstorfer, 1914

–– *A. echerius satellitica Nieuwenhuis, 1946
Range.–– Kep. Banggai (Banggai, Peleng).
–– *A. echerius porphyritica Fruhstorfer, 1914
A. kausambi Felder & Felder, 1860

(Straight Plum Judy – Pl. 8, fig. 37)
Range (1+6+7).–– Burma, Malay Peninsula, Sumatra, Java, Borneo, Palawan (inclu-
ding Balabac and Calamian group: Treadaway, 1995), Sulawesi.
Foodplants.–– Embelia (Myrsinaceae) (Igarashi & Fukuda, 2000, who also illustrate
foodplant and early stages.
–– *A. kausambi sabina Stichel, 1924
Nymphalidae Rafinesque, 1815

(nymphs, browns, milkweeds, admirals, emperors)
Range.–– Cosmopolitan; about 6500 species divided into 9 subfamilies and 4 tribes
incertae sedis (Lamas et al., in prep.), all of which except the Sino-Himalayan Calinagi-
nae are represented in the Sulawesi Region.
Note added in proof. – The classification adopted here may be changed consider-
ably in the near future, particularly with regard to the groups listed here under Biblid-
inae; see Wahlberg et al. (in press).
Foodplants.–– About 100 families of flowering plants; in addition, a small number
of species feed on non-flowering plants (e.g., cycads, lycopods).
Key works.–– Ehrlich (1958), Kristensen (1976), Ackery (1988), Shields (1989a),
Teshirogi (1990), Harvey (1991), Ackery et al. (1999), Brower (2000), Yoshimoto (2001),
Freitas & Brown (submitted), Lamas et al. (in prep).
Libytheinae Boisduval, 1833

(snouts or beaks — Pl. 15, fig. 5)
Range.–– Cosmopolitan. This extremely widespread group consists of 12 species,

usually divided into two genera, one in the New World the other in the Old. Shields
(1989b) maintains that this group should have family status, representing the stem
group of a major butterfly lineage, the Nymphalidae; de Jong et al. (1996) confirm
this relationship, but retain the snouts within the Nymphalidae sensu lato.
Foodplants.–– Ulmaceae.
Key works.–– Pagenstecher (1901), Shields (1985), Okano (1987), Ackery (1988).
Libythea Fabricius, 1807

(beaks — Pl. 15, fig. 5)
Range (W).–– Old World. Seven species, of which two are known from Sulawesi.
Foodplants.–– Ulmaceae.
Key works.–– Pagenstecher (1901), Common & Waterhouse (1981), Shields (1985),
Corbet & Pendlebury (1992).
L. narina Godart, 1819

(White-spotted Beak)
Range (1+3+4+5+6).–– Sikkim to northern Malaysia, Langkawi Islands, Sumatra,
Java, Lesser Sunda Islands, Palawan, northern Philippines (Luzon, Mindoro: Treada-
way, 1995), Sulawesi, N & C Maluku (Halmahera, Obi, Seram), New Guinea (Arfak
Mts: Parsons, 1999: 484). Apparently absent from Borneo and southern Philippines.
–– *L. narina canuleia Fruhstorfer, 1909
L. geoffroy Godart, 1824

(Geoffroy’s, Blue, Purple, Eastern or Australian Beak - Pl. 15, fig. 5)
Range (1+2+3+4+5+6).–– Burma, Indo-China, Java, Lesser Sunda Islands, Man-
galum Island (Sabah), Palawan, Philippines, Sulawesi, N & C Maluku, New Guinea
region, Solomon Islands, New Caledonia, northern Australia.
Foodplants.–– Celtis (Ulmaceae). Igarashi & Fukuda (2000) illustrate all life stages
(Laos).
–– *L. geoffroy celebensis Staudinger, 1889
Morphinae Newman, 1834

(morphos, owls — Pl. 9)
Range.–– Neotropical, Oriental and Australian Regions. About 240 species, divisi-
ble into three tribes (recognised by Ackery, 1988, as separate subfamilies), of which
only one is represented in the Old World.
Foodplants.–– Primarily monocotyledons in the Oriental and Australian Regions.
Key works.–– Ehrlich (1958), DeVries et al. (1985), Ackery (1988).
Amathusiini Moore, 1893

(fauns, kings, saturns, duffers)
Range.–– Oriental and Australian Regions. About 100 species in 13 genera, of which
four are represented in Sulawesi.
Foodplants.–– As subfamily.
Key works.–– Stichel (1912), Kirchberg (1942), Aoki et al. (1982).
Faunis Hübner, 1819

(fauns — Pl. 9, fig. 7)
Range (1+2+6+7).–– Sikkim, Indo-China, Malay Peninsula, Sumatra, Java, Borneo,

Philippines, Sulawesi Region. A medium sized genus of about 15 species, represented
in the Sulawesi Region by a single but polytypic endemic.
Foodplants.–– Arecaceae (Caryota, Phoenix, Pholidocarpus), Liliaceae (Liriope),
Musaceae (Musa), Pandanaceae (Pandanus), Smilacaceae (Smilax).

Key works.–– Stichel (1912), Aoki et al. (1982).
*F. menado Hewitson, 1865

(Sulawesi or Menado Faun — Pl. 9, fig. 7)
Foodplants.–– Arecaceae (unidentified), recorded by Igarashi & Fukuda (2000),
who illustrate the larva and pupa.
–– *F. menado menado Hewitson, 1865
–– *F. menado zenica Fruhstorfer, 1911
–– *F. menado klados Brooks, 1933
–– *F. menado chitone Hewitson, 1862
–– *F. menado fruhstorferi Röber, 1896
–– *F. menado pleonasma Röber, 1896
–– *F. menado intermedius Röber, 1896
–– *F. menado syllus Fruhstorfer, 1911
–– *F. menado sulanus Fruhstorfer, 1899
Amathusia Fabricius, 1807

(palmkings — Pl. 9, figs 1, 4)
Range (1+2+5+6+7).–– Burma, Indo-China, Malay Peninsula, Sumatra, Java, Bali,

Lombok, Borneo, Philippines, Palawan, Sulawesi Region. A genus of about a dozen
butterflies, represented on Sulawesi by one widespread species and one very dis-
tinctive endemic.
Key works.–– Stichel (1912), Eliot (1964a), Aoki et al. (1982).
Amathusia (Amathusia) Fabricius, 1887
Range.–– As genus.
A. (A.) phidippus Linnaeus, 1763

(The Palmking — Pl. 9, fig. 4)
Range (1+2+5+6+7).–– as genus.
Foodplants.–– Borassus, Cocos, Elaeis (Arecaceae); Musa (Musaceae). Igarashi &
Fukuda (1997) illustrate all life stages (Java).
–– *A. (A.) phidippus celebensis Fruhstorfer, 1763

Range.–– Sulawesi, Talisei, Kep. Banggai (Peleng).
*Amathusia (Pseudamathusia) Honrath, 1886
*A. (P.) virgata Butler, 1870

(Honrath’s Palmking — Pl. 9, fig. 1)
–– *A. (P.) virgata thoanthea Fruhstorfer, 1911
Range.–– Sulawesi (N, C, SE).
–– *A. (P.) virgata virgata Butler, 1870
Amathuxidia Staudinger, 1887

(kohinoors — Pl. 9, figs 2, 3)
Range (2+6+7).–– Assam, Indo-China, Malay Peninsula, Sumatra, Java, Borneo,

southern Philippines (Treadaway, 1995), Sulawesi Region. A genus of only two spe-
cies, represented in Sulawesi by an endemic.
*A. plateni Staudinger, 1887

(Platen’s Kohinoor — Pl. 9, figs 2, 3)
–– *A. plateni plateni Staudinger, 1855
–– *A. plateni iamos Brooks, 1937
–– *A. plateni pelengensis Okano, 1986
–– *A. plateni suprema Fruhstorfer, 1899
Discophora Boisduval, 1836

(duffers — Pl. 9, figs 5, 6)

Java, Lombok, Borneo, Philippines, Sulawesi Region. A genus of of 12 or so species
represented in Sulawesi, at the eastern limit of the range, by a single endemic.
Foodplants.–– Arecaceae; Poaceae: Bambuseae (Arundinaria, Bambusa, Dendrocala-
mus, Schizostachyum).
*D. bambusae Felder & Felder, 1867

(Sulawesi Duffer — Pl. 9, figs 5, 6)
–– *D. bambusae bambusae Felder & Felder, 1865
–– *D. bambusae celebensis Holland, 1891
–– *D. bambusae bangkaiensis Fruhstorfer, 1902
Satyrinae Boisduval, 1833 (1820)

(satyrs, browns — Pl. 10)
Range.–– Cosmopolitan. This major group of butterflies, with perhaps 2000 or

more species, is currently divided into six tribes (Harvey, 1991; Lamas et al., in prep.).
Four are represented on Sulawesi, divided among eleven genera.
Foodplants.–– Mostly monocotyledons.
Key works.–– Miller (1968), Corbet & Pendlebury (1992), Aoki et al. (1982), Ackery
(1988).
Melanitini Reuter, 1896

(evening browns — Pl. 10, figs 1-3, 7)
Range.–– Palaeotropical. Five genera, of which two occur in the Sulawesi Region,
one endemic, the other widespread throughout the old world tropics. Vane-Wright
(1995) suggests the possibility of a sixth genus, from Papua New Guinea, based on a
painting by Ellis Rowan.
Note.–– This tribe is referred by Harvey (1991) as the Biini, but with removal of
the monobasic neotropical genus Bia to the Brassolini (Vane-Wright, 1972; DeVries et
al., 1985; Freitas et al., 2002; Lamas et al., in prep.), the correct tribal name for this resi-
dual old world group is Melanitini.
Foodplants.–– Predominantly grasses (Poaceae).
Key works.–– Smiles (1973), Aoki et al. (1982), Uémura (1987).
*Bletogona Felder & Felder, 1867

(celebeans — Pl. 10, figs 1, 2, 7)
Range (E).–– Sulawesi. An endemic genus of just two species. The phylogenetic
relationship of Bletogona to other Melanitini is obscure, but B. mycalesis shares the
same habit of being easily attracted to fruit bait, especially in the evening.
Key works.–– Aoki et al. (1982), Uémura (1987).
*B. mycalesis Felder & Felder, 1867

(Common Celebean — Pl. 10, fig. 1)
–– *B. mycalesis unicolor Martin, 1929
–– *B. mycalesis mycalesis Felder & Felder, 1867

*B. inexspectata [sic!] Uémura, 1987

(New Celebean — Pl. 10, figs 2, 7)
Note.–– Plate 10, fig. 2, illustrates the sexually dimorphic female of this taxon. See
also Uémura (1993).
Melanitis Fabricius, 1807

(evening browns — Pl. 10, fig. 3)
Range (W).–– As tribe. A medium-sized genus of 12 species (R.L. Smiles, unpu-

blished), many of which occur in the Indo-Australian tropics. Seven species have been
found in the Sulawesi Region, each one representing a different distribution pattern.
Foodplants.–– Arecaceae; ?Cyperaceae, Poaceae.
Key works.–– Corbet & Pendlebury (1992), Aoki et al. (1982).
M. leda Linnaeus, 1758

(Common Evening Brown)
Range (W).–– Ethiopian, Oriental, eastern Palaearctic and Australian Regions.
Note.–– The type specimen of obsoleta Felder & Felder, purported to be from Sula-
wesi and formerly regarded to be the local subspecies of M. leda, represents M. zitenius
Herbst, a species not found in the Sulawesi Region.
Foodplants.–– Cocos, Elaeis (Arecaceae); ?Cyperaceae; Apluda, Axonopus, Bambusa,
Brachiaria, Capillipedium, Chrysopogon, Coix, Cyrtococcum, Digitaria, Eleusine, Heteropo-
gon, Imperata, Leersia, Melinis, Microstegium, Miscanthus, Ophiuros, Oplismenus, Oryza,
Panicum, Paspalum, Pennisetum, Poa, Rottboellia, Saccharum, Setaria, Sorghum, Stenotaph-
rum, Themeda, Thysanolaena, Zea, Zizania (Poaceae). Bascombe et al. (1999) illustrate all
life stages (Hong Kong).
–– *M. leda celebicola Martin, 1929
Range.–– Sulawesi, Kep. Sangihe (Sangihe, Siao), Kep. Banggai (Peleng).
–– M. leda leda Linnaeus, 1758
Range.–– Sri Lanka, India, Indo-China, China, Malay Peninsula, Sumatra, Java,
Lesser Sunda Islands, Borneo, Philippines, Tanahjampea, Kalao.
–– M. leda bouruana Holland, 1900
Range.–– Kep. Sula (Mangole), N & C Maluku, New Guinea region.
M. phedima Cramer, 1780

(Dark Evening Brown)
Range (6).–– Sri Lanka to Indo-China and Japan, Malay Peninsula, Sumatra, Java,
Sulawesi.
Foodplants.–– Apluda, Bambusa, Brachiaria, Capillipedium, Coix, Cyrtococcum, Eleusine,
Isachne, Ischaemum, Microstegium, Miscanthus, Oplismenus, Oryza, Panicum, Saccharum,
Setaria, Sorghum, Thysanolaena, Zea (Poaceae). Bascombe et al. (1999) illustrate egg, larva
and pupa (Hong Kong).
–– *M. phedima linga Fruhstorfer, 1908

M. velutina Felder & Felder, 1867

Range (4).–– Sulawesi Region, central Maluku.
–– *M. velutina velutina Felder & Felder, 1867
–– *M. velutina ribbei Röber, 1886
Range.–– Sulawesi (C, S, SE), Kep. Banggai.
–– *M. velutina panvila Fruhstorfer, 1911
M. atrax Felder, 1863

Range (P).–– Philippines (excluding Palawan), Kep. Talaud, Kep. Sangihe.
–– M. atrax pitya Fruhstorfer, 1911
Range.–– Kep. Talaud, Kep. Sangihe (Sangihe, Siao).
M. boisduvalia Felder & Felder, 1863

(Boisduval’s Evening Brown – Pl. 10, fig. 3)
Range (1+2).–– Philippines (including Palawan: Treadaway, 1995), northern Sula-
wesi Region, ?Ternate.
–– *M. boisduvalia ernita Fruhstorfer, 1911
Range.–– Sulawesi (N), Kep. Talaud, Kep. Sangihe (Sangihe, Siao).
M. pyrrha Röber, 1887

Range (3).–– Sulawesi Region, northern Maluku (Bacan), ?Ambon.
–– *M. pyrrha hylecoetes Holland, 1890
–– *M. pyrrha pyrrha Röber, 1887
M. constantia Cramer, 1777

(Constantia Evening Brown)
Range (P).–– Kep. Sula, N & C Maluku, New Guinea region.
Hostplants.–– Imperata (Igarashi & Fukuda , 2000), Saccharum, Setaria (Parsons, 1999)
(Poaceae). Igarashi & Fukuda (2000) illustrate the larva and pupa (Papua New Guinea).
–– *M. constantia salapia Fruhstorfer, 1911
Elymniini Herrich-Schäffer, 1864

(Pl. 10, figs 4-6, 8, 10, 11, 14-16)
Range.–– Predominantly palaeotropical, with relatively weak representation in the

Palaearctic, Nearctic and Neotropical Regions. Divided into four subtribes, all repre-
sented in Sulawesi.
Foodplants.–– Arecaceae, Musaceae, Poaceae (often Bambuseae).
Key works.–– Miller (1968), Ackery (1988).
Elymniina Herrich-Schäffer, 1864
Range.–– Palaeotropics. Two genera, one in Africa, the other in the Indo-Austra-
lian region.
Elymnias Hübner, 1818

(palmflies — Pl. 10, fig. 4)
Range (W).–– Oriental and Australian Regions. Over 40 species, represented in the
Sulawesi Region by five endemics.
Foodplants.–– Arecaceae (Archontophoenix, Areca, Arenga, Calamus, Caryota, Chry-
salidocarpus, Cocos, Cyrtostachys, Elaeis, Licuala, Livistonia, Metroxylon, Phoenix, Pinanga,
Ptychosperma, Rhapis, Roystonea, Trachycarpus), Musaceae (Musa), Orchidaceae (Acriop-
sis: Igarashi & Fukuda, 1997).
*E. cumaea Felder & Felder, 1867

(Pl. 10, fig. 4)
–– *E. cumaea cumaea Felder & Felder, 1867
–– *E. cumaea toliana Fruhstorfer, 1899
–– *E. cumaea resplendens Martin, 1929
–– *E. cumaea bornemanni Ribbe, 1889
–– *E. cumaea phrikonis Fruhstorfer, 1899
*E. sangira Fruhstorfer, 1899

Range (L).–– Kep. Sangihe (Sangihe, Siao), Kep. Talaud.
*E. mimalon Hewitson, 1862

–– *E. mimalon mimalon Hewitson, 1862
–– *E. mimalon ino Fruhstorfer, 1894
–– *E. mimalon nysa Fruhstorfer, 1907
*E. hicetas Wallace, 1869

–– *E. hicetas rarior Martin, 1929

–– *E. hicetas hicetas Wallace, 1869
–– *E. hicetas bonthainensis Fruhstorfer, 1899
–– *E. hicetas hicetina Fruhstorfer, 1904
Range.–– Sulawesi (C, SE).
–– *E. hicetas butona Fruhstorfer, 1904
Range.–– Buton.
*E. hewitsoni Wallace, 1869

(Hewitson’s Palmfly)
Range (R).–– southern Sulawesi, Salayar.
–– *E. hewitsoni hewitsoni Wallace, 1869
–– *E. hewitsoni atys Fruhstorfer, 1907
–– *E. hewitsoni meliophila Fruhstorfer, 1896
Zetherina Reuter, 1896
Range.–– Indo-China, Philippines (excluding Palawan) and Sulawesi. Two genera,

one of which occurs on Sulawesi.
Zethera Felder, 1861

(wallaceans — Pl. 10, fig. 6)
Range (2).–– Philippines (excluding Palawan: C. G. Treadaway, pers. comm.),

Sulawesi. Six species.
Foodplants.–– Poaceae (Dinochloa).
Key works.–– Vane-Wright & Smiles (1975), Aoki et al. (1982), Roos (1992).
*Z. incerta Hewitson, 1861

(Great Wallacean — Pl. 10, fig. 6)
–– *Z. incerta incerta Hewitson, 1869
–– *Z. incerta tenggara Roos, 1992
Z. musa Felder & Felder, 1861

Range.–– Philippines (Mindanao, Basilan), ?Sulawesi Region.
–– Z. musa subsp. (Vane-Wright & Smiles, 1975)
Range.–– ?Kep. Talaud.
Lethina Reuter, 1896
Range.–– As tribe. A large group of 20 or more genera, but with only one represen-
ted in Sulawesi.
Foodplants.–– ?Arecaceae, Cyperaceae, Poaceae.
Lethe Hübner, 1819

(foresters and tree-browns — Pl. 10, fig. 5)
Range (W).–– Sri Lanka to China, Philippines, Maluku and Lesser Sunda Islands.
A genus of more than 60 species, including many in Asia, but only two (which are
probably closely related) in Sulawesi.
Foodplants.–– Cyperaceae (rare), Poaceae (mainly Bambuseae).
L. europa Fabricius, 1775

(Bamboo Tree-brown — Pl. 10, fig. 5)
Range (W).–– India, Indo-China, Malay Peninsula, Sumatra, Java, western Lesser
Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region, N & C Maluku.
Foodplants.–– Bambusa, Dinochloa, Microstegium, Phyllostachys, Pleioblastus (Poace-
ae). Igarashi & Fukuda (1997) illustrate the larva and pupa (Philippines); Bascombe et
al. (1999) illustrate all life stages (Hong Kong).
–– *L. europa arcuata Butler, 1868
Range.–– Sulawesi (N, C, SE), Kep. Banggai (Peleng).
–– *L. europa nagaraja Fruhstorfer, 1911
Range.–– Sulawesi (S), Salayar.
–– *L. europa velitra Fruhstorfer, 1911
Range.–– Kep. Sangihe, Kep. Talaud.
–– *L. europa anatha Fruhstorfer, 1911
*L. violae Tsukada & Nishiyama, 1979

(Violet Tree-brown)
Mycalesina Reuter, 1896
Range.–– Palaeotropics. A group of about 12 genera, of which four occur in the

Indo-Australian region, including the very large Mycalesis; two of the genera are ende-
mic to the Sulawesi Region.
Orsotriaena Wallengren, 1858

(niggers, or jungle browns — Pl. 10, fig. 8)
Range (W).–– Oriental and Australian Regions. Two species, both present in
Sulawesi.
Key works.–– Aoki et al. (1982).
O. medus Fabricius, 1775

(The Nigger)
Range (W).–– Sri Lanka, southern India, Nepal, Sikkim, Indo-China, Malay Penin-
sula, Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi
Region, N & C Maluku, New Guinea region, Solomon Islands.
Foodplants.–– Imperata, Oryza, Oplismenus, Panicum (in captivity), Saccharum
(Poaceae). Igarashi & Fukuda (1997) illustrate all life stages (Philippines).
–– O. medus medus Fabricius, 1775
Range.–– As species, including Sulawesi, Kep. Talaud (Salebabu), Kep. Sangihe
(Sangihe, Siao), Salayar, Tanahjampea, Kep. Tukangbesi (Binongko, Kaledupa), Kep.
Banggai (Peleng), but not Sri Lanka, southern India, Nicobars, Mentawi Islands, nort-
hern Queensland and Bismarcks.
Note: H. Gaonkar (pers. comm.) considers that the true type locality for medus is
southern India; the nomenclature of the subspecies will therefore need revision.
*O. jopas Hewitson, 1864

(Sulawesi Jungle Brown — Pl. 10, fig. 8)
–– *O. jopas jopas Hewitson, 1864
Range.–– Sulawesi (N, C, SE), Kep. Talaud, ?Kep. Banggai.
Note.–– Nieuwenhuis (1946) states that jopas does not occur in Kep. Banggai.
–– *O. jopas mendice Fruhstorfer, 1911
–– *O. jopas paupercula Fruhstorfer, 1908
Range.–– Kep. Bowokan, Kep. Sula (Mangole, Sanana).
Mycalesis Hübner, 1818

(bush browns — Pl. 10, figs 10, 11)
Range (W).–– Oriental and Australian Regions. A large genus of perhaps 100 or
more species, still in need of much revision; seven species have been found in the
Sulawesi Region.
*M. itys Felder, 1867

(Itys Bush Brown — Pl. 10, fig. 10)
Foodplants.–– Paniscum psilopodium (Igarashi & Fukuda, 2000), who also illustrate
the larva and pupa.
–– *M. itys itys Felder, 1867
–– *M. itys remulina Fruhstorfer, 1897

Range.–– Sulawesi (N, C, S, SE).
–– *M. itys sulensis Grose Smith & Kirby, 1896
M. janardana Moore, 1858

(Common Bush Brown, Janardana Bush Brown)
Range (2+3+5+6+7).–– Malay Peninsula, Sumatra, Java, Bali, Lombok, Borneo,
southern Philippines (Treadaway, 1995), Sulawesi Region, northern Maluku.
Foodplants.–– Digitaria, Oplismenus, Paspalum (Poaceae). Igarashi & Fukuda (2000)
illustrate all life stages.
–– *M. janardana opaculus Fruhstorfer, 1908
Range.–– Sulawesi, Kep. Sangihe (Sangihe), Salayar.
–– *M. janardana besina Fruhstorfer, 1908
Range.–– Kep. Sula (Mangole, Sanana, ?Bowokan).
M. perseus Fabricius, 1775

(Dingy Bush Brown)
Range (W).–– Sri Lanka, India, China, Burma, Malay Peninsula, Sumatra, Java,
Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region, Maluku, New
Guinea region, Solomon Islands, northern Australia. Uémura (1985b) includes this
and the next three species in the mineus species group, a group of about 20 species dis-
tributed from Sri Lanka to Vanuatu.
Foodplants.–– Axonopus (in captivity), Dichanthium, Heteropogon, Imperata, Oplis-
menus (in captivity), Oryza, Panicum (in captivity), Themeda; also on introduced Pani-
cum in Australia (all Poaceae). Igarashi & Fukuda (1997) illustrate all life stages (Phi-
lippines).
–– M. perseus lalassis Hewitson, 1864
Range.–– Sulawesi, Tanahjampea, Kep. Tukangbesi (Kaledupa), Kep. Banggai
(Peleng), Kep. Sula (Mangole, Sanana), N & C Maluku, New Guinea region, Solomon
Islands.
M. horsfieldi Moore, 1892

(Horsfield’s Bush Brown)
Range (1+6+7).–– Malay Peninsula, Sumatra, Java, Bali, Borneo, Palawan, Sulu
Archipelago (Treadaway, 1995), Sulawesi Region.
Note.–– Aoki et al. (1982) and Uémura (1985b) place newayana Fruhstorfer as a
separate endemic species from southern Sulawesi; we treat it here as a subspecies of
horsfieldi. For a description of the female, see Uémura (1993).
Foodplants.–– Imperata, Oryza, Panicum, Saccharum (Poaceae). Igarashi & Fukuda
(2000) illustrate all life stages
–– *M. horsfieldi tessimus Fruhstorfer, 1908
Range.–– Sulawesi (N), Kep. Banggai (Peleng), ?Kep. Sula.
–– *M. horsfieldi newayana Fruhstorfer, 1911
Range.–– Sulawesi (S), Kabaena.
–– *M. horsfieldi ptyleus Fruhstorfer, 1908
M. mynois Hewitson, 1864

(Pl. 10, fig. 11)
Range (5).–– Lesser Sunda Islands (Lombok to Timor), Tanahjampea, Sulawesi (S).
–– *M. mynois subsp. (Zoölogisch Museum, Amsterdam)
Range.–– Tanahjampea, Sulawesi (S). The identity of this material, much darker
than typical mynois, requires further investigation.
M. mineus Linnaeus, 1758

(Dark-brand Bush Brown)
Range (P).–– Sri Lanka, India, China, Japan, Malay Peninsula, Sumatra, Java, Les-
ser Sunda Islands, Borneo, Palawan, Philippines (absent from Mindanao region:
Uémura, 1985b; Treadaway, 1995), Kalao, Tanahjampea.
Foodplants.–– Eleusine, Leersia, Lophatherum, Microstegium, Pogonatherum, Saccha-
rum, Thysanolena (Poaceae). Bascombe et al. (1999) illustrate all life stages (Hong
Kong).
–– *M. mineus subsp. (BMNH)
M. sirius Fabricius, 1775

(Cedar Bush Brown)
Range (P).–– Kep. Sula, C Maluku, New Guinea region, Australia.
Foodplants.–– Imperata, Ischaemum, Panicum, Themeda; also on introduced Panicum
in Australia (all Poaceae).
–– *M. sirius subsp. (BMNH)
*Lohora Moore, 1880

(Sulawesi browns — Pl. 10, figs 15, 16)
Range (R).–– Sulawesi Region, including Kep. Sangihe, Kep. Banggai, Kep. Sula,
Kabaena and Buton. The largest generic group of butterflies endemic to the Sulawesi
Region, all 17 species would formerly have been included within Mycalesis. Separation
of Lohora may render Mycalesis paraphyletic. Reliable recognition of a number of Loho-
ra taxa, notably those related to ophthalmicus, seems difficult. Unlike most Mycalesis,
Lohora species show little differentiation of the male genitalia.
Foodplants.–– Undoubtedly various Poaceae, including Centotheca (Igarashi &
Fukuda, 2000).
Key works.–– Aoki et al. (1982), Vane-Wright & Fermon (2003).
*Lohora (Lohora) Moore, 1880
Range.–– As genus, but not known from Kep. Sula.

*L. (L.) dexamenus Hewitson, 1862

*L. (L.) transiens Fruhstorfer, 1908

Range (R).–– Sulawesi (C, SE; see Roos, 1995), Buton, Kabaena (Vane-Wright &
Fermon, 2003).
*L. (L.) dinon Hewitson, 1864

*L. (L.) tilmara Fruhstorfer, 1906

Range (L).–– Kep. Sangihe (Sangihe, Siao).
*L. (L.) anna Vane-Wright & Fermon (2003)

=Lohora deianira Hewitson, [1862], sensu Aoki et al. 1982, nec Hewitson.
Misidentification.
Range (E).–– Sulawsei (C).
*L. (L.) ophthalmicus Westwood, 1888

Range (R).–– Sulawesi (N, C), Talisei, Lembeh.
Foodplants.–– Centotheca longilamina (Poaceae), recorded by Igarashi & Fukuda
(2000), who also illustrate all life stages.
*L. (L.) unipupillata Fruhstorfer, 1898

Range (E).–– Sulawesi (C, SE).
*L. (L.) haasei Röber, 1887

Range (L).–– Kep. Banggai (Peleng).
*Lohora (Physcon) de Nicéville, 1898
Range.–– Sulawesi and Kep. Sula.

Foodplants.–– Unknown, probably Poaceae.
*L. (Ph.) inga Fruhstorfer, 1899

Range (L).–– Kep. Sula (Mangole, Sanana).
*L. (Ph.) pandaea Hopffer, 1874

*L. (Ph.) deianirina Fruhstorfer, 1897

Range.–– Sulawesi (N, C). See Vane-Wright & Fermon (2003) regarding taxonomic
status.
*L. (Ph.) decipiens Martin, 1929

*L. (Ph.) umbrosa Roos, 1997

Range (E).–– Sulawesi (SE).
*L. (Ph.) deianira Hewitson, 1862

*L. (Ph.) imitatrix Martin, 1929

(Pl. 10, fig. 16)
*L. (Ph.) erna Fruhstorfer, 1898

*Lohora (Pseudomycalesis) Tsukada & Nishiyama, 1979

Foodplants.–– unknown.
L. (Ps.) tanuki Tsukada & Nishiyama, 1979

(Pl. 10, fig. 15)
Range (E).–– Sulawesi (C, E).
*Nirvanopsis Vane-Wright, new name

= Nirvana Tsukada & Nishiyama, 1979, not Nirvana Kirkaldy, 1900
(Hemiptera: Cicadellidae)
(Pl. 10, fig. 14)
Range (E).–– Sulawesi (C, E).

This beautiful monobasic genus appears to be very closely related to Lohora (Vane-
Wright & Fermon, 2003); its status may have to be re-assessed after a cladistic analysis
of the Mycalesina.
Key works.–– Aoki et al. (1982).
*N. hypnus Tsukada & Nishiyama, 1979

(The Hypnotist — Pl. 10, fig. 14)
Range (E).–– as genus.
Ragadiini Herrich-Schäffer, 1864

(Pl. 10, figs 12, 13)
Range.–– Assam, Indo-China, Malay Peninsula, Sumatra, Java, Borneo, Palawan,

Philippines, Sulawesi Region, northern Maluku and Irian Jaya. Two genera, one of
which occurs in Sulawesi; the two only overlap in the Philippines.
Foodplants.–– Selaginellaceae.
Key works.–– Aoki et al. (1982), Vane-Wright (1990), Igarashi & Fukuda (1997).
Acrophtalmia Felder, 1861

(pale ringlets — Pl. 10, figs 12, 13)
Range (2+3+4).–– Philippines (excluding Palawan), Sulawesi Region, Buru, nort-

hern Maluku, Irian Jaya. About five or six species occur in the Philippines, one or two
in Sulawesi, and one in Maluku. The Allyn Museum of Entomology (Florida) has
three male specimens of an Acrophtalmia from the Arfak Mts, Irian Jaya, which appear
to represent an endemic race of A. chione Felder & Felder, the Maluku taxon (L. & J.
Miller, pers. comm.).
Hostplants.–– Selaginellaceae (Selaginella).
Key works.–– Uémura & Yamaguchi (1982), Aoki et al. (1982), Igarashi & Fukuda
(1997).
*A. leuce Felder & Felder, 1867

(Pl. 10, fig. 13)
Range (R).–– Sulawesi Region (excluding S).
Foodplants.–– Selaginella delicatula (Igarashi & Fukuda, 2000), who also illustrate
the larva and pupa.
–– *A. leuce leuce Felder & Felder, 1867
–– *A. leuce banggaaiensis Nieuwenhuis, 1946
–– *A. leuce chionides de Nicéville, 1900
*A. windorum Miller & Miller, 1978

(Pl. 10, fig. 12)
The status and distribution of this taxon requires investigation; the late A. Bedford
Russell (pers. comm.) considered it to be a subspecies of leuce.
Satyrini Boisduval, 1833 (1820)

(browns, graylings, ringlets — Pl. 10, fig. 9)
Range.–– Cosmopolitan. Ten subtribes are recognised, of which only one is repre-
sented in the Sulawesi Region.
Foodplants.–– Mostly Poaceae.
Key works.–– Miller (1968), Ackery (1988).
Ypthimina Reuter, 1896
Range.–– Palaeotropics, with weak extension into the Palaearctic Region. Of the
dozen or more genera, only one occurs in Sulawesi.
Foodplants.–– Cyperaceae, Juncaceae, Poaceae, Restoniaceae, Zingiberaceae.
Ypthima Hübner, 1818

(rings — Pl. 10, fig. 9)
Range (W).–– Palaeotropics, including Australia if Xois arctous is included (see

Shirôzu & Shima, 1979; Parsons, 1999: 567). A large genus of more than 100 species.
Shima (1988) recognised two subgenera, both represented in the Sulawesi Region (one
by a single endemic species, the other by seven, five of which are endemic).
Hostplants.–– Various genera of Poaceae.
Key works.–– Corbet & Pendlebury (1992), Shirôzu & Shima (1979), Aoki et al.
(1982), Uémura (1982; 1985a, 1999), Shima (1988).
Ypthima (Thymipa) Moore, 1893

(rings)
Range.–– Oriental Region, about 40 species divided by Shima (1988) into three
species groups, one of which extends eastwards through the Malay Archipelago to N
Maluku and Timor.
Foodplants.–– Poaceae (including Miscanthus, Oplismenus, Pogonatherum).
*Y. (T.) nynias Fruhstorfer, 1911

Range (R).–– Sulawesi Region. A member of the philomela-group (Shima, 1988), a
group of about ten species distributed from Sri Lanka to China and Japan, and
through the Malay Archipelago to the Philippines, Sulawesi Region, northern Maluku
and Timor.
–– *Y. (T.) nynias nynias Fruhstorfer, 1911
Range.–– Sulawesi, Muna, Buton.
–– *Y. (T.) nynias aretas Fruhstorfer, 1911
–– *Y. (T.) nynias gadames Fruhstorfer, 1911
Ypthima (Ypthima) Hübner, 1818

(rings)
Range.–– Palaeotropics, including part of Pacific, and with some extension into
southern Palaearctic. Over 60 species, many African, divided by Shima (1988) into
nine groups, two of which are represented in the Sulawesi Region.
Foodplants.–– Poaceae (including Bambusa, Cynodon, Digitaria, Ehrharta, Imperata,
Microstegium, Oplismenus, Paspalum, Pogonatherum).
Y. (Y.) norma Westwood, 1851

Range (4+5).–– Burma, Indo-China, China, northern Philippines (north Luzon:
Treadaway, 1995), Lesser Sunda Islands, southern Sulawesi Region, central Maluku
(Buru, Ambon). A member of the asterope-group (Shima, 1988), richly represented in
the Afrotropical Region, but with only two species in the Orient, extending east from
India to central Maluku and the Lesser Sunda Islands.
–– Y. (Y.) norma pusilla Fruhstorfer, 1911

Range.–– Sulawesi (C, S), Buton, Buru, Ambon.
Y. (Y.) kalelonda Westwood, 1888

Range (3).–– Sulawesi Region, northern Maluku. This and the remaining five Ypt-
hima belong to the pandocus-group (Shima, 1988; Uémura, 1999), about a dozen species
with a collective distribution extending from Thailand through the Malay Archipela-
go to Bali, Borneo, Philippines, Sulawesi Region and northern Maluku.
–– *Y. (Y.) kalelonda kalelonda Westwood, 1888
Range.–– Sulawesi (N), Talisei.
–– *Y. (Y.) kalelonda celebensis Rothschild, 1892
–– *Y. (Y.) kalelonda anana Fruhstorfer, 1911
–– *Y. (Y.) kalelonda mangolina Uémura, 1982
*Y. (Y.) risompae Uémura, 1982

Foodplants.–– Unknown in nature, Miscanthus (in captivity) (Poaceae) (Igarashi &
Fukuda, 1997, who also illustrate larva and pupa).
*Y. (Y.) ancus Fruhstorfer, 1911

*Y. (Y.) gavalisi Martin, 1913

(Pl. 10, fig. 9)
*Y. (Y.) junkoae Uémura, 1999

*Y. (Y.) loryma Hewitson, 1865

Foodplants.–– Unidentified species of Poaceae (Igarashi & Fukuda, 1997, who also
illustrate larva and pupa).
Charaxinae Guénée, 1865

(charaxids — Pl. 11, figs 1, 2)
Range.–– cosmotropical, with moderate extension into temperate regions. Six tri-
bes, of which two occur in the Indo-Australian region, with only one represented in
Sulawesi.
Foodplants.–– Recorded from more than 30 families of flowering plants, notably the
Convolvulaceae, Fabaceae, Flacourtiaceae, Euphorbiaceae, Piperaceae, Sapindaceae.
Key works.–– Rydon (1971), Corbet & Pendlebury (1992), Ackery (1988), Teshirogi
(1990), Tsukada (1991).
Charaxini Guénée, 1865

(nawabs, rajahs)
Range.–– Palaeotropics. Two major genera, both present in Sulawesi.

Foodplants.–– A variety of families, with Fabaceae most characteristic.
Key works.–– As subfamily.
Charaxes Ochsenheimer, 1816

(rajahs, pashas — Pl. 11, fig. 1)
Range (W).–– Palaeotropics with some extension into temperate regions. The
genus is most richly represented in Africa (by 152 species: Henning, 1989); about 25
occur in the Indo-Australian region.
Foodplants.–– Annonaceae, Euphorbiaceae, Fabaceae, Lauraceae, Meliaceae,
Rutaceae (Oriental representatives only).
Key works.–– Corbet & Pendlebury (1992), Tsukada (1991).
C. latona Butler, 1865

(Orange Emperor)
Range (P).–– Kep. Sula, northern Maluku, New Guinea region including Bougain-
ville, and northern Australia (Common & Waterhouse, 1981).
Foodplants.–– Dalbergia, Pterocarpus (Fabaceae); Aglaia, Dysoxylum (Meliaceae);
Cryptocarya, Litsea (Lauraceae). Parsons (1999) illustrates all life stages (Papua New
Guinea).
–– *C. latona artemis Rothschild, 1900
*C. nitebis Hewitson, 1862

(Green Rajah)
–– *C. nitebis nitebis Hewitson, 1862
–– *C. nitebis sulaensis Rothschild, 1900
Range.–– Kep. Banggai (Peleng), Kep. Sula (Mangole, Sanana, Taliabu).
*C. affinis Butler, 1865

Foodplants.–– Manihot (Euphorbiaceae) (recorded by Igarashi & Fukuda, 1997,
who illustrate the larva and pupa), and Persea americana (Lauraceae) (recorded by Tes-
hirogi, 2001, who also illustrates the larva and pupa).
–– *C. affinis affinis Butler, 1865
Range.–– Sulawesi, Kep. Togian.
–– *C. affinis butongensis Tsukada, 1991
Range.–– Buton, Kabaena.
–– *C. affinis spadix Tsukada, 1991
*C. musashi Tsukada, 1991

(Sulawesi Tawny Rajah)
*C. mars Staudinger, 1885

(Iron Rajah)
Note.–– Nieuwenhuis (1959) described the female, also illustrated by Tsukada
(1991). C. m. dohertyi Rothschild, 1892, is a synonym (Tsukada, 1991); C. madensis Roth-
schild, 1899, from Buru, which has been treated as a subspecies of C. mars, is evidently
a separate, very distinct species.
*C. setan Detani, 1983

(Black Rajah)
Range (L).–– Kep. Banggai (Peleng).
C. solon Fabricius, 1793

(Wise Rajah)
Range (1+2+7).–– Sri Lanka, India, Burma, Thailand, Malay Peninsula, Sumatra,
Borneo, Palawan, Philippines, Sulawesi Region.
Foodplants.–– Acacia, Dalbergia, Moullava, Pithecellobium, Tamarindus, Wagatea,
Xylia (Fabaceae). Igarashi & Fukuda (1997) illustrate the larva and pupa (Philippines).
–– *C. solon hannibal Butler, 1869
–– *C. solon catulus Fruhstorfer, 1914
Range.–– Siao, Kep. Sangihe, Kep. Talaud.
–– *C. solon brevis Tsukada, 1991
Range.–– Buton.
–– *C. solon iliona Tsukada, 1991
–– *C. solon mangolianus Rothschild, 1900
C. bernardus Fabricius, 1793

(Pl. 11, fig. 1)
Range.–– Sri Lanka, Peninsular India, Nepal to south China, Malay Peninsula,
Sumatra, Java, Bali, Bawean, Kangean, Borneo, ?Sulawesi.
Foodplants.–– Various Annonaceae, Euphorbiaceae, Fabaceae, Lauraceae, and
Rutaceae noted by Igarashi & Fukuda (1997), who also illustrate all life stages (Hong
Kong).
–– C. bernardus repetitius Butler, 1896
Range.–– Borneo, ?N Sulawesi.
Note.–– Four male specimens in BNMH possibly from Sulawesi, apparently from
three independent sources but all with poor data (one indicates “Menado”), are phe-
notypically very similar or identical to Bornean C. bernardus repetitius. So far as we are
aware, this species was not collected during the Project Wallace expedition, and Tsuka-
da (1991) does not record it from Sulawesi. Generally similar in appearance to the
endemic C. affinis, these BMNH bernardus specimens probably have false data. Unfor-
tunately, before this anomaly was realised, the “Menado” specimen was photograp-
hed as the representative Charaxes to be illustrated.
Polyura Billberg, 1820

(nawabs — Pl. 11, fig. 2)
Range (W).–– Oriental, Australian and Pacific Regions. About 27 species, of which
three occur on Sulawesi.
Foodplants.–– Anonaceae (Annona), Clusiaceae (Mesua), Connaraceae (Rourea),
Euphorbiaceae (Bridelia), Fabaceae (Abarema, Acacia, Adenanthera, Albizia, Archidendron,
Caesalpinia, Cassia, Cynometra, Delonix, Leucaena, Millettia, Moullava, Pararchidendron,
Paraserianthes, Parkia, Peltophorum, Pithecellobium, Poinciana, Robinia, Senna, Wagatea,
Wisteria), Fagaceae (Castanopsis), Lauraceae (Cinnamomum), Lythraceae (Lagerstroemia),
Oleaceae (Jasminium), Rhamnaceae (Rhamnella, Ventilago), Rhizophoraceae (Bruguiera,
Rhizophora), Rosaceae (Prunus, Rosa), Sapindaceae (Nephelium), Simaroubaceae (Guil-
foylia), Sterculiaceae (Brachychiton, Sterculia, Theobroma), Tiliaceae (Grewia), Ulmaceae
(Celtis, Trema), Verbenaceae (Tectona).
Key works.–– Common & Waterhouse (1981), Smiles (1982), Tsukada (1985, 1991),
Teshirogi (1990), Corbet & Pendlebury (1992).
*P. inopinatus Röber, 1939

Note.–– Described by Röber (1940) from a single male from Tondano, this distinc-
tive taxon was overlooked by Smiles (1982). Tsukada (1991: 236) reproduces the ori-
ginal colour illustration; so far as we are aware, no further material of this beautiful
species has come to light.
*P. cognata Vollenhoven, 1861

(Sulawesi Blue Nawab — Pl. 11, fig. 2)
–– *P. cognata cognata Vollenhoven, 1861
Range.–– Sulawesi (N, C, and including SE: Roos, 1995)
–– *P. cognata bellona Tsukada, 1991
Range.–– Sulawesi (S), Kep. Tukangbesi (Hanafusa, 1985).
–– *P. cognata yumikoe Nishimura, 1984
P. alphius Staudinger, 1886

(Staudinger’s Nawab)
Range (5+6).–– India, Nepal, Burma, Java, Lesser Sunda Islands, Sulawesi. Otsuka
(1988) included this Sulawesi butterfly within P. athamas, but Smiles (1982) had sepa-
rated it as a distinct species under the name agraria Swinhoe, 1887. Tsukada (1991)
placed the two disjunct groups of populations grouped by Smiles under the older
name alphius Staudinger.
–– *P. alphius piepersianus Martin, 1924

Range.–– Sulawesi (probably S only).
P. galaxia Butler, 1865

(Kalao Nawab)
Range (P).–– Lesser Sunda Islands (Lombok to Tanimbar), Kalao.
–– *P. galaxia kalaonicus Rothschild, 1898
Biblidinae Boisduval, 1833

(Pl. 12, figs 6-12; Pl. 13, figs 1-10; Pl. 14, figs 1, 5)
Range.–– More usually known as the “Limenitinae” or “Limenitidinae” (e.g. Har-

vey, 1991), this large group of well over 1000 species and 100 genera (Ackery et al.,
1999) is now widely regarded as a paraphyletic or even polyphyletic assemblage (e.g.
Brower, 2000). The artificial combination is maintained here, under the senior name
Biblidinae, awaiting a definitive proposal for their re-classification (e.g. Wahlberg et
al., in press). Here we recognise four tribes: Cyrestini incertae sedis, Biblidini, Pseu-
dergolini incertae sedis, and Limenitidini incertae sedis. The last named tribe will proba-
bly prove to be very distinct, but even with its exclusion, the first three are not likely
to form a natural group.
Foodplants.–– See individual tribes.
Key works.–– Ackery (1988), Teshirogi (1990), Harvey (1991), Corbet & Pendlebu-
ry (1992), Ackery et al. (1999), Brower (2000), Wahlberg et al. (in press), Freitas & Brown
(submitted).
Cyrestini Guénée, 1865, incertae sedis

(map wings — Pl. 13, figs 5, 7)
Range.–– Three genera in the palaeotropics (but not Australia), two of which repre-
sented on Sulawesi, with a fourth, perhaps doubtfully related genus in the New World
(Marpesia). Freitas & Brown (submitted) have proposed to include this group within the
resurrected Biblidinae. Parsons (1999), placed Cyrestis and its allies in the Apaturinae.
Wahlberg et al. (in press) propose promoting the map wings to subfamily rank, the
Cyrestinae, to include the Cyrestini and Pseudergolini as its constituent tribes.
Foodplants.–– Dilleniaceae, Moraceae.
Key works.–– Holloway (1973), Ackery (1988), Teshirogi (1990), Corbet & Pendle-
bury (1992), Parsons (1999), Brower (2000).
Chersonesia Distant, 1883

(maplets — Pl. 13, fig. 5)
Range (1+2+6+7).–– Northern India, Indo-China, China, Malay Peninsula, Suma-

tra, Java, Borneo, Palawan, Philippines, Sulawesi Region. About seven species, one of
which occurs in Sulawesi.
Foodplants.–– Moraceae.
Key works.–– Holloway (1973), Tsukada (1985), Corbet & Pendlebury (1992).
C. rahria Moore, 1858

(Wavy Maplet — Pl. 13, fig. 5)
Range (1+6+7).–– Thailand, Malay Peninsula, Sumatra, Java, Bali, Borneo, Pala-
wan, Sulawesi Region.
Foodplants.–– Ficus (Moraceae). Igarashi & Fukuda (1997) illustrate the larva and
pupa (Malaya).
–– *C. rahria celebensis Rothschild, 1892
Range.–– Sulawesi (including SE: Roos, 1995), Kep. Togian.
–– *C. rahria banggaina Tsukada & Nishiyama, 1985
–– *C. rahria mangolina Fruhstorfer, 1899
Cyrestis Boisduval, 1832

(map wings — Pl. 13, fig. 7)
Range (W).–– Oriental Region to China and Japan, and Malaya Archipelago to the
Solomons and New Caledonia, but absent from Australia. A genus of perhaps 25 spe-
cies, depending on taxonomic limits (see Parsons, 1999: 582), of which five occur in the
Sulawesi Region, three of them exhibiting eastern links to Maluku and the Papuan
Region. See also Introduction and fig. 13.
Foodplants.–– Dilleniaceae, Moraceae.
Key works.–– Holloway (1973), Tsukada (1985), Teshirogi (1990), Corbet & Pendle-
bury (1992), Parsons (1999).
C. paulinus Felder & Felder, 1860

(Paulinus Map)
Range (3+4).–– Sulawesi Region, N & C Maluku, New Guinea (Vogelkop).
Foodplants.–– Streblus ilicifolius (Moraceae), recorded by Igarashi & Fukuda (2000),
who also illustrate all life stages.
–– *C. paulinus mantilis Staudinger, 1886
Range.–– Sulawesi (N, C), Kep. Togian (Dolong).
–– *C. paulinus kransi Jurriaanse & Lindemans, 1920
Range.–– Butung, Wowoni.
–– *C. paulinus kuehni Röber, 1886
–– *C. paulinus seneca Wallace, 1869
*C. heracles Staudinger, 1896

Range (R).–– Sulawesi, Kep. Sula, Salayar.
–– *C. heracles heracles Staudinger, 1896
Range.–– Sulawesi (N, C), Kep. Sula (Mangole).
–– *C. heracles selayarensis Hanafusa, 1993
C. thyonneus Cramer, 1779

(Pl. 13, fig. 7)
Range (4).–– Sulawesi Region, central Maluku. Appears closely related to C. there-
sae, from Sumatra and Borneo.
–– *C. thyonneus celebensis Staudinger, 1896
Range.–– Sulawesi, Kabaena.
–– *C. thyonneus pelensis Detani, 1983
–– *C. thyonneus sulaensis Staudinger, 1896
*C. eximia Oberthür, 1879

Range (L).–– Kep. Sangihe (Sangihe, Tona Tahuna, Siao).
*C. strigata Felder & Felder, 1867

(Celebes Map)
Range (R).–– Sulawesi Region. This species is intimately related to the acilia-group
(Tsukada, 1985), which is distributed from Buru to the Solomon Islands.
Foodplants.–– Streblus (Moraceae) (recorded by Igarashi & Fukuda, 1997, who also
illustrate larva and pupa).
–– *C. strigata strigata Felder & Felder, 1867
Range.–– Sulawesi, Kep. Togian (Dolong), Kabaena, Wowoni, Butung.
–– *C. strigata parthenia Röber, 1887
–– *C. strigata bettina Fruhstorfer, 1899
Biblidini Boisduval, 1833

(Pl. 12, figs 10-12)
Range.–– Mainly Neotropical, but also Afrotropical and Oriental Regions, east to
Maluku. Up to 40 genera included, just two of which occur on Sulawesi. Freitas &
Brown (submitted) propose to place this group within the resurrected subfamily Bibli-
dinae. Harvey (1991) divided the group into seven subtribes, only one of which occurs
in the Sulawesi Region. Wahlberg et al. (in press) likewise recognise these seven tribes,
within the resurrected subfamily Biblidinae sensu stricto.
Foodplants.–– Casuarinaceae, Euphorbiaceae, Malvaceae, Passifloraceae (in Orien-
tal Region).
Key works.–– Ackery (1988), Teshirogi (1990), Harvey (1991), Corbet & Pendlebu-
ry (1992), Brower (2000).
Eurytelina Doubleday, 1845
Range.–– Palaeotropics. Two of the nine genera occur in Sulawesi.

Foodplants.–– Mainly Euphorbiaceae.
Ariadne Horsfield, 1829

(castors — Pl. 12, figs 10, 11)
Range (W).–– Oriental Region including Lesser Sunda Islands, Philippines, Sula-
wesi Region and N & C Maluku. A genus of about 14 species, 5 of which occur in Afri-
ca, and 4 are found in the Sulawesi Region.
Foodplants.–– Casuarinaceae, Euphorbiaceae, Malvaceae, Passifloraceae (Adenia:
Igarashi & Fukuda, 1997).
Key works.–– Tsukada (1985), Teshirogi (1990), Corbet & Pendlebury (1992).
A. ariadne Linnaeus, 1763

(Angled Castor)
Range (P).–– Sri Lanka, India, Indo-China, China, Japan, Malay Peninsula, Suma-
tra, Java, Lesser Sunda Islands, Borneo, Butung, Muna, Kabaena.
Foodplants.–– Acalypha, Cnesmone, Ricinus, Tragia (Euphorbiaceae). Teshirogi
(1990) (Japan) and Igarashi & Fukuda (1997) (Malaya) illustrate all life stages, as do
Bascombe et al. (1999) (Hong Kong).
–– A. ariadne gedrosia Fruhstorfer, 1912
Range.–– Lesser Sunda Islands, Butung, Muna, Kabaena.
A. specularia Fruhstorfer, 1899

Range (P).–– Thailand (Otsuka, 1988; Pinratana & Eliot, 1996), Malay Peninsula,
Sumatra, Java, Lesser Sunda Islands, Borneo, Kalao.
–– *A. specularia intermedia Fruhstorfer, 1899
Range.–– Sumbawa, Alor, Kalao.
*A. celebensis Holland, 1891

(Celebes Castor — Pl. 12, fig. 10)
–– *A. celebensis dongalae Fruhstorfer, 1903
–– *A. celebensis subsp. (Roos, 1995)
–– *A. celebensis celebensis Holland, 1891
*A. merionoides Holland, 1891

(Holland’s Castor — Pl. 12, fig. 11)
–– *A. merionoides merionoides Holland, 1891
Range.–– Sulawesi, Talisse, Butung, Kabaena.
–– *A. merionoides pecten Tsukada, 1985
–– *A. merionoides sulaensis Joicey & Talbot, 1922
Laringa Moore, 1901

(dandies — Pl. 12, fig. 12)
Range (1+6+7).–– Burma, Malay Peninsula, Sumatra, Java, Borneo, Palawan, Sula-
wesi. Two species, one of which has been found in Sulawesi.
Key works.–– Tsukada (1985), Corbet & Pendlebury (1992).
L. castelnaui Felder & Felder, 1860

(Blue Dandy — Pl. 12, fig. 12)
Range (1+6+7).–– Thailand, Malay Peninsula, Sumatra, Java, Borneo, Palawan,
Sulawesi.
–– *L. castelnaui subsp. (d’Abrera, 1985)
Pseudergolini Jordan, 1898, incertae sedis

(Pl. 13, figs 8, 9)
Range.–– Indo-Australian region, extending to Japan (but not Australia). A small

group of four or five genera (see Morishita, 1995), two of which occur on Sulawesi.
This tribal group has long been included in the “Limenitidinae”, but its correct
position could be within the Apaturinae (Pinratana & Eliot, 1996; Parsons, 1999). Tes-
hirogi (1990) proposed placing Dichorragia in a separate subfamily, the Dichorragiinae,
while Harvey (1991) placed it in the Cyrestini. Igarashi & Fukuda (1997) noted a stri-
king peculiarity of both Pseudergolis and Dichorragia, whereby the first-instar larvae
make, at the edge of a leaf, a rod-like structure fashioned from chewed leaf fragments,
and then rest along the underside of this fine projection. However, the precise inter-
pretation of this behaviour may be problematic, as Parsons (1999: 581) describes the
process rather differently, and notes that identical or very similar behaviour is also
exhibited by the early instars of some Cyrestis, which he also included in the Apaturi-
nae. The work of Brower (2000) offers little support for a close link between the Apa-
turinae and Cyrestis. Here we maintain the Pseudergolini sensu Morishita (1995) as a
separate tribe, incertae sedis within the Biblidinae. Wahlberg et al. (in press) propose to
include the Pseudergolini as a second tribe within a newly-promoted subfamily Cyre-
stinae.
Foodplants.–– Anacardiaceae, Burseraceae, Meliosmaceae, Urticaceae.
Key works.–– Ackery (1988), Teshirogi (1990), Corbet & Pendlebury (1992), Moris-
hita (1995), Pinratana & Eliot (1996), Fukuda & Igarashi (1997), Parsons (1999).
Dichorragia Butler, 1869

(constables — Pl. 13, fig. 8)
Range (W).–– Northern India, Thailand, China, Taiwan, Japan, Malay Peninsula,
Sumatra, Java, Lesser Sundas, Borneo, Palawan, Philippines, Sulawesi Region,
Maluku, New Guinea region. Two allopatric species.
Foodplants.–– Anacardiaceae (Smiles in litt: Parsons, 1999), Burseraceae (Canarium:
Igarashi & Fukuda, 1997), Meliosmaceae.
Key works.–– d’Abrera (1977), Teshirogi (1990), Tsukada (1991), Corbet & Pendle-
bury (1992).
D. nesimachus Doyère, 1840

(The Constable — Pl. 13, fig. 8)
Range (1+2+3+5+6+7).–– Northern India, Thailand, China, Taiwan, Japan, Malay
Peninsula, Sumatra, Java, Bali, Lombok, Borneo, Palawan, Philippines, Sulawesi
Region, N Maluku.
Foodplants.–– Meliosma (Meliosmaceae). Teshirogi (1990) (Japan) and Igarashi &
Fukuda (1997) (Taiwan) illustrate all life stages, as do Bascombe et al. (1999) (Hong
Kong).
–– *D. nesimachus pelurius Fruhstorfer, 1897
–– *D. nesimachus harpalycus Fruhstorfer, 1913
–– *D. nesimachus peisandrus Fruhstorfer, 1913
Pseudergolis Felder & Felder, 1867

(tabbies — Pl. 13, fig. 9)
Range (D).–– India, China, Burma, Thailand, Sulawesi. The disjunct distribution of
the three species comprising this small genus led Corbet & Pendlebury (1978) to spe-
culate it “must once have occurred in Sundaland, where it is now apparently extinct.”
Pseudergolis is a distinctive genus, offering the only example of a distribution pattern
of this type in the Sulawesi butterfly fauna.
Foodplants.–– Urticaceae.
Key works.–– Tsukada (1991); Pinratana & Eliot (1996), Harada (1997), Fukuda &
Igarashi (1997).
*P. avesta Felder & Felder, 1867

(Sulawesi Tabby — Pl. 13, fig. 9)
Range (R).–– Sulawesi, Butung.
Foodplants.–– Pipturus argenteus (Urticaceae), recorded by Igarashi & Fukuda
(2000), who also illustrate the larva and pupa.
–– *P. avesta avesta Felder & Felder, 1867
–– *P. avesta toalarum Fruhstorfer, 1912
–– *P. avesta nimbus Tsukada, 1991
Range.–– Butung.
Limenitidini Behr, 1864, incertae sedis

(admirals, sergeants, commanders — Pl. 13, figs 1-4, 6, 10; Pl. 14, figs 1, 5)
Range.–– Cosmopolitan. A large, distinct and diverse assemblage of many species,

in over 40 genera. Harvey (1991) divided the group into four subtribes, all of which
are represented on Sulawesi. As noted above, the Limenitidines almost certainly do
not belong to the Biblidinae, but no definitive reclassification has yet been published.
Wahlberg et al. (in press) propose to recognise the four subtribes of Harvey as tribes,
within the subfamily Limenitidinae sensu stricto.
Foodplants.–– Numerous families, including Anacardiaceae, Bombacaceae, Capri-
foliaceae, Clusiaceae, Euphorbiaceae, Fabaceae, Fagaceae, Hypericacae, Loranthaceae,
Naucleaceae, Oleaceae, Passifloraceae, Rhamnaceae, Rubiaceae, Salicaceae, Sapindace-
ae, Sterculiaceae, Ulmaceae and Urticaceae.
Key works.–– Chermock (1950), Ackery (1988), Corbet & Pendlebury (1992).
Limenitidina Behr, 1864

(admirals, sergeants, commanders — Pl. 14, figs 1, 5)
Range.–– Cosmopolitan. A large group of species in about 20 genera, 5 of which

occur on Sulawesi.
Foodplants.–– Principally Caprifoliaceae, Naucleaceae, Rubiaceae, Salicaceae,
Ulmaceae, Urticaceae.
Key works.–– Chermock (1950), Ackery (1988), Corbet & Pendlebury (1992).
Tarattia Moore, 1898

(commanders — not illustrated)
Range (1+2+7).–– Northern Borneo, Palawan, Philippines, Sulawesi Region. Four

species, separated from Moduza and placed in the resurrected genus Tarattia by Hana-
fusa (1989) and Tsukada (1991), two of which occur in the Sulawesi Region.
Foodplants.–– Rubiaceae (Wendlandia) (Igarashi & Fukuda, 2000).
Key works.–– Tsukada (1991).
*T. lysanias Hewitson, 1859

–– *T. lysanias lysanias Hewitson, 1859
Range.–– Sulawesi, Kabaena.
–– *T. lysanias aberrans Hanafusa, 1989
Range.–– Muna.
–– *T. lysanias hiromii Hanafusa, 1989
–– *T. lysanias karschi Fruhstorfer, 1912
*T. bruijni Oberthür, 1879

Range (L).–– Kep. Sangihe.
Note.–– Incorrectly spelled ‘brujini’ by Tsukada (1991)
Athyma Westwood, [1850]

(sergeants — Pl. 14, fig. 5)
Range (1+2+5+6+7).–– India (including Andamans), China, Japan, Malay Archi-

pelago to Palawan, Philippines, Sulawesi, Java, Lesser Sunda Islands (to Flores) and
Sulawesi Region. Athyma includes about 15-20 species (Tsukada, 1985; Bascombe et al.,
1999); the single Sulawesi representative has only recently been placed in the genus
(Igarashi, 1997).
Foodplants.–– Euphorbiaceae, Oleaceae, Rubiaceae (Adina, Mussaenda: Bascombe
et al., 1999).
Key works.–– Tsukada (1991), Corbet & Pendlebury (1992), Igarashi (1997).
*A. libnites Hewitson, 1859

(Pl. 14, fig. 5)
Foodplants.–– Glochidion philippicum (Euphorbiaceae), as recorded by Igarashi &
Fukuda (2000), who illustrate all life stages.
–– *A. libnites libnites Hewitson, 1859
–– *A. libnites noctesco Tsukada, 1991
Range.–– Butung, Muna, Kabaena.
–– *A. libnites nieuwenhuisi Hanafusa, 1989
Moduza Moore, 1881

(commanders — not illustrated)
Range (1+2+5+6+7).–– Indo-Australian region eastwards to Palawan, Philippines,

Sulawesi Region, Lesser Sundas and ?C Maluku. A small group of about 12 species
(Bascombe et al., 1999) none of which occurs further east than the Moluccas (and
Maluku requires confirmation); represented on Sulawesi by two endemic species.
Foodplants.–– Rubiaceae (Mussaenda, Nauclea, Timonias, Uncaria, Wendlandia).
Key works.–– Tsukada (1991), Corbet & Pendlebury (1992), Igarashi (1997).
*M. lymire Hewitson, 1859

–– *M. lymire lymire Hewitson, 1859
–– *M. lymire munaensis Hanafusa, 1989
Range.–– Muna, Butung.
–– *M. lymire nectareus Tsukada, 1991
–– *M. lymire citatus Tsukada, 1991
Range.–– Kep. Togian (Waleabahi).
–– *M. lymire potens Hanafusa, 1989
–– *M. lymire neolymira Fruhstorfer, 1913

*M. lycone Hewitson, 1859

–– *M. lycone lycone Hewitson, 1859
–– *M. lycone lyconides Fruhstorfer, 1913
Range.–– Sulawesi (S), Butung, Wowoni, Muna.
–– *M. lycone kojimai Detani, 1983 (= obatratus Tsukada, 1991)
–– *M. lycone nubilus Tsukada, 1991
*Lamasia Moore, 1898

(not illustrated)
Range (R).–– Sulawesi Region. Tsukada (1991) has recently separated this species
from Moduza, in the resurrected monobasic genus Lamasia.
Key works.–– Tsukada (1991).
*L. lyncides Hewitson, 1859

–– *L. lyncides lyncides Hewitson, 1859
–– *L. lyncides eutenia Fruhstorfer, 1913
–– *L. lyncides togiana Tsukada, 1991
Range.–– Kep. Togian.
–– *L. lyncides notus Tsukada, 1991
Range.–– Muna.
–– *L. lyncides amarapta Fruhstorfer, 1913
Tacola Moore, 1898

(sergeants — Pl. 14, fig. 1)
Range (1+2+4+6+7).–– Malay Peninsula, Sumatra, Java, Borneo, Palawan, sout-

hern and central Philippines, Sulawesi Region, northern and central Maluku. Until
recently the single Sulawesi representative (T. eulimene) was included in the genus
Athyma Westwood (e.g. Corbet & Pendlebury, 1992), a widespread group of about 15
species. Tsukada (1991), however, placed it in the resurrected genus Tacola, to include
also A. magindana and A. larymna.
Key works.–– Tsukada (1985, 1991).
T. eulimene Godart, 1824

(Sulawesi Sergeant — Pl. 14, fig. 1)
Range (3+4).–– Sulawesi Region, N & C Maluku (Buru, Ambon, Seram, Obi,
Bacan: Tsukada, 1991).
–– *T. eulimene badoura Butler, 1866
–– *T. eulimene hegelochus Fruhstorfer, 1913
–– *T. eulimene symphelus Fruhstorfer, 1913
Range.–– Kep. Sula (Taliabu, Sanana).
Neptina Newman, 1870

(aeroplanes, sailers, lascars — Pl. 12, figs 6-9)
Range.–– Palaearctic, Afrotropical, Oriental and Australian Regions. Five genera

are recognised, one widespread in the Old World, the others restricted to the Indo-
Pacific. Four of these genera occur in Sulawesi and, with one exception, all of the spe-
cies are local endemics - and that exception (Pantoporia antara) extends only as far as
Buru where, according to Eliot (1969), “it must be a recent arrival from the Sula Is.,
since it has not yet developed strong subspecific characters.”
Foodplants.–– Bombacaceae, Clusiaceae, Fabaceae, Sterculiaceae, Ulmaceae (in the
Austro-Orient).
Key works.–– Eliot (1969).
Pantoporia Hübner, 1819

(lascars, planes, aeroplanes — Pl. 12, fig. 6)
Range (W).–– Oriental and Australian Regions, including N & C Maluku. About
14 species, only one of which occurs in the Sulawesi Region.
Note.–– Pinratana & Eliot (1996) place Pantoporia as a subgenus of Neptis.
Foodplants.–– Fabaceae (Abarema, Acacia, Albizia, Archidendron, Austroteenisia, Dal-
berga, Derris, Kuntsleria, Lonchocarpus, Parkia, Pithecellobium); Poaceae (Isachne: Igarashi
& Fukuda, 1997); ?Sapindaceae (Braby, 2000).
Key works.–– Eliot (1969), Common & Waterhouse (1981), Tsukada (1985), Corbet
& Pendlebury (1992).
P. antara Moore, 1858

(Pl. 12, fig. 6)
Range (3+4).–– Sulawesi Region, Maluku (Buru, Bacan).
–– *P. antara antara Moore, 1858
–– *P. antara pytheas Fruhstorfer, 1913
Range.–– Sulawesi (C, S), Kep. Tukangbesi (Kapolla, Kaledupa), Kabaena, Butung.
–– *P. antara sulana Eliot, 1969
Range.–– Kep. Banggai (Peleng), Kep. Sula.
Lasippa Moore, 1898

(lascars — Pl. 12, fig. 7)
Range (1+2+6+7).–– Oriental Region, extending eastwards to the Philippines and

Sulawesi Region; absent from Lesser Sunda Islands. About 10 species, one of which
occurs in Sulawesi.
Note.–– Pinratana & Eliot (1996) place Lasippa as a subgenus of Neptis.
Foodplants.–– Hypericaceae (Cratoxylon), Combretaceae (Quisqualis), Fabaceae
(Dalbergia), Rhamnaceae (Ventilago).
Key works.–– Eliot (1969), Tsukada (1985), Corbet & Pendlebury (1992).
*L. neriphus Moore, 1889

(Pl. 12, fig. 7)
Foodplants.–– Ventilago oblongifolia (Rhamnaceae), as recorded by Igarashi &
Fukuda (2000), who also illustrate the larva and pupa.
–– *L. neriphus tawayana Fruhstorfer, 1899
Range.–– Sulawesi, Kep. Togian (“Dolong”), Kep. Banggai (Peleng), Butung, Kaba-
ena, Muna.
–– *L. neriphus sangira Fruhstorfer, 1908
–– *L. neriphus neriphus Hewitson, 1868
Neptis Fabricius, 1807

(sailers, planes, aeroplanes — Pl. 12, figs 8, 9)
Range (1+2+5+6+7).–– Afrotropical, Oriental, Australian and southern Palaearctic

Regions. In addition to a major (and distinctive) group of Neptis in the Afrotropical
Region, there are about 70 species distributed through the south-eastern Palaearctic
and Indo-Australian area (with only one species in Australia itself). A maximum of
four Neptis occur in the Sulawesi Region. So far as we are aware, the genus is not posi-
tively recorded from N & C Maluku (although Parsons, 1999, includes “Moluccas”),
other than Kep. Sula and Gebe.
Foodplants.–– Aceraceae, Bombacaceae, Convolvulaceae, Corylaceae, Fabaceae,
Lauraceae, Malvaceae, Moraceae, Rosaceae, Sterculiaceae (Parsons, 1999), Tiliaceae,
Ulmaceae, Urticaceae, ?Verbenaceae (Parsons, 1999) (Indo-Australian records only).
Key works.–– Eliot (1969), Tsukada (1985), Teshirogi (1990), Corbet & Pendlebury
(1992).
*N. celebica Moore, 1899

(Celebes Sailer — Pl. 12, fig. 8)
–– *N. celebica oresta Fruhstorfer, 1913
–– *N. celebica celebica Moore, 1899

–– *N. celebica arachroa Fruhstorfer, 1913
N. cymela Felder & Felder, 1863

Range.–– Philippines (excluding Palawan), ?Sulawesi.
–– *N. cymela anemorcia Fruhstorfer, 1913
Range.–– ?Sulawesi (very doubtful; requires confirmation).
*N. ida Moore, 1858

(Pl. 12, fig. 9)
Note.–– There is considerable confusion surrounding the subspecific taxonomy
of this insect; we have followed Tsukada (1985), not Eliot (1969), but extensive mate-
rial in the ZSBS suggests that ida s.str. applies to a bright southern race with narrow
hindwing submarginal spots, celebensis applies to a bright Minahassa race with
broad hindwing submarginal spots, and that other northern, central and south-eas-
tern populations are mostly dull (white markings “sullied”) and referable to carbo-
nespersa Martin, 1924.
Foodplants.–– Desmodium (Fabaceae) (recorded by Igarashi & Fukuda, 1997, who
also illustrate larva and pupa).
–– *N. ida ida Moore, 1858
–– *N. ida celebensis Hopffer, 1874
Range.–– Sulawesi (N, C), Kep.Togian, Kep. Banggai (Peleng).
–– *N. ida sphaerica Fruhstorfer, 1907
–– *N. ida saleyra Fruhstorfer, 1908
–– *N. ida liliputa Martin, 1924
Range.–– Butung, Muna, Kabaena.
–– *N. ida kalidupa Eliot, 1969
Range.–– Kep. Tukangbesi (Kaledupa)
N. hylas Linnaeus, 1758

(Common Sailer)
Range (P).–– Sri Lanka, India, China, Japan, Indo-China, Malay Peninsula, Suma-
tra, Java, Lesser Sunda Islands, Borneo, Sulu islands, Tanahjampea, Bonerate, Kalao,
Kep. Tukangbesi.
Foodplants.–– Numerous genera in ?Bombacaceae, Fabaceae (Canavalia, Crotalaria,
Desmodium, Flemingia, Lathyrus, Lespedeza, Mucuna, Paracalyx, Psophocarpus, Pueraria,
Rhynchosia, Tadehagi, Vigna), ?Icacinaceae, Malvaceae, Moraceae (Broussonetia), ?Ster-
culiaceae, Tiliaceae, Ulmaceae (Trema). Teshirogi (1990) and Igarashi & Fukuda (1997)
illustrate all life stages (Japan), as do Bascombe et al. (1999) (Hong Kong).
–– N. hylas timorensis Röber, 1891
Range.–– Lesser Sunda Islands (except Flores to Pura), Tanahjampea, Bonerate,
Kalao, Kep. Tukangbesi (Kaledupa).
Phaedyma Felder, 1861

(sailers, planes, aeroplanes — not illustrated)
Range (1+2+3+4+5+6).–– Oriental Region, extending to central China, Lesser

Sunda Islands, Palawan, Philippines, Sulawesi Region, N & C Maluku, New Guinea
region, Solomon Islands, and northern and eastern Australia, but absent from Borneo.
About a dozen species, represented on Sulawesi by a single endemic.
Note.–– Pinratana & Eliot (1996) place Phaedyma as a subgenus of Neptis.
Foodplants.–– Bombacaceae (Bombax), Boraginaceae (Cordia, Ehretia: Braby, 2000),
Hypericaceae (Cratoxylon), Fabaceae (Dalbergia, Desmodium, Mucuna, Pongamia, Ptero-
carpus, Pteroloma, Tadehagi), Rhamnaceae (Sageretia), Sterculiaceae (Brachychiton, Reeve-
sia, Sterculia), Tiliaceae (Grewia: Braby, 2000), Ulmaceae (Aphananthe, Celtis), Verbe-
naceae (Petraeovitex).
Key works.–– Eliot (1969), Tsukada (1985), Corbet & Pendlebury (1992).
*P. daria Felder & Felder, 1867

–– *P. daria daria Felder & Felder, 1867
–– *P. daria hiereia Fruhstorfer, 1913
Range.–– Sulawesi (C), Kep. Banggai (Peleng).
–– *P. daria albescens Rothschild, 1892
Range.–– Sulawesi (C, S), Kabaena.
–– *P. daria osima Fruhstorfer, 1913
Parthenina Reuter, 1896

(clippers — Pl. 13, fig. 4)
Range.–– Oriental and Australian Regions, to Solomon Islands (but not Australia).
Two genera, one restricted to India-Sundaland.
Foodplants.–– ?Cucurbitaceae, ?Menispermaceae, Passifloraceae.
Key works.–– Corbet & Pendlebury (1992).
Parthenos Hübner, 1819

(clippers — Pl. 13, fig. 4)
Range (1+2+3+4+6+7).–– Oriental and Australian Regions, from Sri Lanka to the
Solomon Islands, but absent from the Lesser Sunda Islands and Australia. A small
genus with one very widespread species and, in the eastern part of the range, two
further species.
Key works.–– d’Abrera (1977), Corbet & Pendlebury (1992).
P. sylvia Cramer, 1775

(The Clipper — Pl. 13, fig. 4)
Range (1+2+3+4+6+7).–– Sri Lanka, India, China, Thailand, Malay Peninsula,
Sumatra, Java, Borneo, Palawan, Philippines, Sulawesi Region, N & C Maluku, New
Guinea region, Solomon Islands.
Foodplants.–– ?Cucurbitaceae (Parsons, 1999); ?Tinospora (Menispermaceae); Ade-
nia, Passiflora (Passifloraceae) (Ackery, 1988; Parsons, 1999: 588; Igarashi & Fukuda,
2000). Igarashi & Fukuda (2000) also illustrate all life stages (Malaya).
–– *P. sylvia salentia Hopffer, 1874
–– *P. sylvia sangira Talbot, 1932
–– *P. sylvia bangkaiensis Fruhstorfer, 1913
–– *P. sylvia sulana Fruhstorfer, 1898
Adoliadina Doubleday, 1845

(dukes, barons, counts — Pl. 13, figs 1-3, 6, 10)
Range.–– Palaeotropics. About a dozen genera, with five occurring in the Indo-
Australian Region - of which all but the Oriental Tanaecia occur in Sulawesi.
Foodplants.–– Mainly found on Anacardiaceae, Clusiaceae, Euphorbiaceae, Fag-
aceae, Loranthaceae and Sapindaceae.
Key works.–– Ackery (1988), Corbet & Pendlebury (1992).
Lexias Boisduval, 1832

(archdukes — Pl. 13, fig. 2)
Range (1+2+3+4+6+7).–– Oriental Region eastwards to Java, Philippines, Sulawesi

Region, N & C Maluku and the New Guinea region. A genus of about a dozen species,
divisible into two groups, the Moluccan and Oriental. Sulawesi has a representative of
the Oriental group, while the Moluccan species occurs in the eastern part of the Sula-
wesi Region.
Foodplants.–– Clusiaceae (Calophyllum, Garcinia), Hypericacae (Cratoxylum).
Key works.–– d’Abrera (1977), Tsukada (1991), Corbet & Pendlebury (1992).
*L. aeetes Hewitson, 1861

–– *L. aeetes aeetes Hewitson, 1861
–– *L. aeetes phasiana Butler, 1870
–– *L. aeetes satellita Jurriaanse & Lindemans, 1920
Range.–– Sulawesi (C - Tsukada, 1991), Wowoni.
–– *L. aeetes butongensis Tsukada, 1991
Range.–– Butung, Kabaena.
–– *L. aeetes rubellio Fruhstorfer, 1898
L. aeropa Linnaeus, 1764

(Orange-banded Plane)
Range (P).–– Kep. Sula, N & C Maluku, New Guinea region, including northern
tip of Queensland.
Foodplants.–– Calophyllum (Clusiaceae: Braby, 2000).
–– *L. aeropa orestias Fruhstorfer, 1913
Euthalia Hübner, 1819

(barons, counts, duchesses, earls, marquesses — Pl. 13, figs 1, 6)
Range (1+2+5+6+7).–– Oriental Region, from Sri Lanka eastwards to China, Java,
Lesser Sunda Islands, Philippines and Sulawesi Region. A genus of over 20 species,
divided into the aconthea and lubentina species groups. The former is represented on
Sulawesi by E. aconthea itself (only recently discovered there: Müller, 1994), and the
latter by an endemic species found on Sulawesi and various nearby islands, and a
further endemic restricted to the Sula Archipelago.
Note.–– Pinratana & Eliot (1996) and Yokochi (1999b) include within Euthalia a
number of groups separated by Tsukada and others as full genera.
Foodplants.–– Anacardiaceae, Asteraceae, Cucurbitaceae, Dipterocarpaceae, Ebe-
naceae, Euphorbiaceae, Fagaceae, Loranthaceae, Melastomataceae, Moraceae, Rosace-
ae, Sapindaceae.
Key works.–– Talbot (1943), Tsukada (1991), Corbet & Pendlebury (1992), Igarashi
& Fukuda (1997), Yokochi (1999a,b,c,d).
E. aconthea Cramer, 1777

(The Baron)
Range (1+5+6+7).–– Sri Lanka, S India and N India eastwards to southern China,
Malay Peninsula, Andamans, Sumatra, Java, Kangean, Lesser Sunda Islands, Palawan,
SW Philippines (Bongao, Sibutu, Jolo) and Sulawesi.
–– *E. aconthea bakrii Müller, 1994
*E. amanda Hewitson, 1862

(Sulawesi Gaudy Baron — Pl. 13, figs 1, 6)
Foodplants.–– Scurrula (Loranthaceae: recorded by Igarashi, 1994, and Igarashi &
Fukuda, 1997, who also illustrate larva and pupa).
–– *E. amanda amanda Hewitson, 1862 (= rubicundus Tsukada, 1991; see Yokochi, 1999c)
Range.–– Sulawesi, Kabaena, Butung, Muna (Yokochi, 1999d), WangiWangi.
–– *E. amanda selayarensis Tsukada, 1991
Range.–– Salayar. The male is described by Yokochi (1996).
–– *E. amanda subsp. (BMNH)
–– *E. amanda periya Fruhstorfer, 1913
Range.–– Kep. Banggai (Peleng). Lectotype designated by Yokochi (1999c).
*E. amabilis Staudinger, 1896

Range (L).–– Kep. Sula (Mangole, Sanana, Taliabu: Yokochi, 1999d).
Yokochi (1999a) selected a lectotype from Mangole, in Zoologisches Museum der
Humboldt Universität, Berlin. Euthalia amanda sulaensis Talbot, 1943, is a synonym
(lectotype designated by Yokochi, 1999c).
Dophla Moore, 1880

(dukes — Pl. 13, fig. 3)
Range (1+2+6+7).–– Sri Lanka, India, Indo-China, Hainan, Malay Peninsula,

Sumatra, Java, Borneo, Palawan, Philippines, Sulawesi Region. Pinratana & Eliot
(1996) and Yokochi (1999b) place the monobasic Dophla as a subgenus of Euthalia.
Foodplants.–– Anacardiaceae, Ebenaceae, Euphorbiaceae, Fagaceae.
Key works.–– Corbet & Pendlebury (1992).
D. evelina Stoll, 1790

(Redspot Duke — Pl. 13, fig. 3)
Foodplants.–– Anacardium (Anacardiaceae), Diospyros (Ebenaceae), Antidesma
(Euphorbiaceae), Lithocarpus (Fagaceae). Igarashi & Fukuda (1997) illustrate all life sta-
ges (Malaya).
–– *D. evelina bolitissa Fruhstorfer, 1913
–– *D. evelina dermoides Rothschild, 1892
Range.–– Sulawesi (N, C), Salayar, Kabaena.
–– *D. evelina bangkaiana Fruhstorfer, 1904
–– *D. evelina fumosa Fruhstorfer, 1899
Bassarona Moore, 1897

(marquesses — Pl. 13, fig. 10)
Range (1+2+5+6+7).–– Oriental Region, from Assam to Java, Flores, Philippines

and Sulawesi. A small genus represented in the Sulawesi Region by a single endemic.
Pinratana & Eliot (1996) and Yokochi (1999b) place Bassarona as a subgenus of
Euthalia.
*B. labotas Hewitson, 1864

(Sulawesi Marquis — Pl. 13, fig. 10)
Range (R).–– Sulawesi, Butung, Kep. Banggai.
–– *B. labotas labotas Hewitson, 1864
–– *B. labotas pallesco Tsukada, 1991
Range.–– Butung.
–– *B. labotas pelengensis Yokochi, 1990

Apaturinae Boisduval, 1840

(Pl. 15, figs 1-4)
Range.–– Cosmopolitan (but absent from Australia). Over 400 species in about 22
genera, 20 of which occur in the Old World, 6 in Malaysia, and 4 on Sulawesi. Addi-
tionally, Pinratana & Eliot (1996) include the four genera of the Pseudergolini within
this subfamily (see also Parsons, 1999: 581; Lamas et al. in prep.).
Foodplants.–– Betulaceae, Carpinaceae, Fagaceae, Salicaceae, Ulmaceae.
Key works.–– Le Moult (1950), Rydon (1971), DeVries et al. (1985), Ackery (1988),
Teshirogi (1990), Corbet & Pendlebury (1992), Pinratana & Eliot (1996).
Rohana Moore, 1880

(black princes — Pl. 15, fig. 1)
Range (1+2+6+7).–– Sri Lanka, India, China, Burma, Thailand, Malay Peninsula,
Sumatra, Java, Bali, Borneo, Palawan, Philippines, Sulawesi. A small group of five or
six species, with a single representative in Sulawesi.
Foodplants.–– Ulmaceae (Celtis).
Key works.–– Le Moult (1950), Nguyen-Phung (1985), Tsukada (1991), Corbet &
Pendlebury (1992).
*R. macar Wallace, 1869

(Wallace’s Black Prince — Pl. 15, fig. 1)
Range (R).–– Sulawesi Region. Until resurrected by Tsukada (1991), this taxon was
generally included as a subspecies within R. rhea Felder (Philippines, including Pala-
wan).
–– *R. macar macar Wallace, 1869
Range.–– Sulawesi, Muna, Kep. Banggai (Peleng: Nieuwenhuis, 1946).
–– *R. macar butongensis Tsukada, 1991
Range.–– Buton.
Helcyra Felder, 1860

(white emperors — Pl. 15, fig. 2)
Range (3+4+5+6+7).–– Northern India, Thailand, China, Taiwan, Sumatra, Java,

Lesser Sunda Islands, Borneo, Philippines (Luzon), Sulawesi, northern and central
Maluku, New Guinea region. Rare butterflies with partly discontinuous distributions.
Parsons (1999) considered that there were only four species, but Le Moult (1950) listed
five, one having been found on Sulawesi. A species from Luzon, noted in Treadaway
(1995), was described by Tsukada (1991), and a Lesser Sundas subspecies (of H.
hemina) by Kotaki (1985). Masui & Inomata (1992) recognised seven species.
Key works.–– Evans (1932), Le Moult (1950), d’Abrera (1977), Tsukada (1991),
Masui & Inomata (1992), Masui (1999).
*H. celebensis Martin, 1913

(Sulawesi White Emperor — cf. Pl. 15, fig. 2)
Range (R).–– Sulawesi, Kep. Banggai. Until separated by Tsukada (1991), this
taxon was regarded as a subspecies of H. hemina Hewitson, from SE Asia, Sumatra,
Java and Borneo.
–– *H. celebensis celebensis Martin, 1913 (= c. australis Tsukada, 1991)
Range.–– Sulawesi (C, N, S).
–– *H. celebensis fabulose Tsukada, 1991
–– *H. celebensis semifusca Masui, 1999
Range.–– Buton.
Hestinalis Bryk, 1938

(sorcerers — Pl. 15, fig. 3)
Range (2+6).–– Northern India, China, Malay Peninsula, Sumatra, Java, Philippi-
nes (not Palawan), Sulawesi. This interesting genus comprises a number of apparently
mimetic butterflies, and has an unusual distribution. Formerly included in Hestina
Westwood, the single Sulwesi endemic was placed by Le Moult (1950; see also Moris-
hita, 1997), together with two other former Hestina species, in the genus Hestinalis
Bryk. Tsukada (1991) extended this usage to cover at least six species.
Key works.–– Le Moult (1950), Teshirogi (1990), Tsukada (1991), Corbet & Pendle-
bury (1992).
*H. divona Hewitson, 1851

(Sulawesi Sorcerer — Pl. 15, fig. 3)
Range (E).–– Sulawesi (N, C; see Roos, 1995).
Euripus Doubleday, 1848

(courtesans — Pl. 15, fig. 4)
Range (1+2+6+7).–– Northern India, Indo-China, Malay Peninsula, Sumatra, Java,

Bali, Borneo, Palawan, Philippines, Sulawesi. Another small but interesting genus,
with a total of about five species, represented on Sulawesi by a single endemic.
Foodplants.–– Ulmaceae (Celtis, Trema), Urticaceae.
Key works.–– Le Moult (1950), Tsukada (1991), Corbet & Pendlebury (1992).
*E. robustus Wallace, 1869

(Wallace’s Courtesan — Pl. 15, fig. 4)
Nymphalinae Rafinesque, 1815

(admirals, pansies, leaf-butterflies — Pl. 14, figs 2-4, 6-12)
Range.–– Cosmopolitan. A major group, with perhaps 50 or more genera divided

into four tribes, two of which are represented in the Sulawesi Region.
Foodplants.–– A variety of flowering plant families, but mainly Acanthaceae and
Urticaceae.
Key works.–– Ackery (1988), Nakanishi (1988), Teshirogi (1990), Harvey (1991),
Brower (2000), Nylin et al. (2001).
Nymphalini Rafinesque, 1815

(admirals, jesters, painted ladies, tortoiseshells, commas — Pl. 14, figs 3, 6, 7, 10, 11)
Range.–– As subfamily. About a hundred species, a number of them very familiar

and frequently referred to as “vanessids” (a synonym), are included in this cosmopoli-
tan group. Three of the 13 genera occur in the Sulawesi Region.
Foodplants.–– Largely as subfamily, but Kaniska has apparently “host shifted” to
various Liliales.
Symbrenthia Hübner, 1819

(jesters — Pl. 14, figs 6, 7, 11)
Range (W).–– Oriental, south-eastern Palaearctic and Australian Regions (but not
Australia). Five of the known species occur on Sulawesi. Parsons (1999) considers
there to be 13 species, but due to taxonomic problems the total is very uncertain. Here
we follow Tsukada (1985) and Motono & Negishi (1989) in applying the name lilaea,
but not hippoclus, to one of the species found on the Asian mainland. Koiwaya (1989)
applied hippoclus (type-locality Ambon) to a species that includes China within its
range. Parsons (1999) apparently applies hippoclus to a taxon occuring from India and
China through the Malay Archipelago, as far east as Bougainville. We treat hippoclus
here as a species extending from Thailand to Maluku. Note added in proof: Fric et al.
(submitted) now propose to include the formerly separate Papuan region genus
Mynes within Symbrenthia, bringing the group to over two dozen species. The bioge-
ographic implications of their work, which for all five Sulawesi species are very inte-
resting, are noted briefly in the introductory section, under “cladistic analysis.”
Foodplants.–– Urticaceae.
Key works.–– Holloway (1973), Tsukada (1985), Corbet & Pendlebury (1992),
Parsons (1999), Fric et al. (submitted).
S. lilaea Hewitson, 1864

(Common Jester)
Range (2+5+6+7).–– Northern India, China, Thailand, Malay Peninsula, Sumatra,
Java, Bali, Lombok, Borneo, Philippines (excluding Palawan), Sulawesi.
Foodplants.–– Boehmeria, Debregeasia, Girardinia (Urticaceae). Bascombe et al. (1999)
illustrate all life stages (Hong Kong).
–– *S. lilaea utakata Tsukada & Nishiyama, 1985
S. hippoclus Cramer, 1779

Range (W).–– Thailand, Malay Peninsula, Sumatra, western Lesser Sunda Islands,
Borneo, Palawan, Philippines, Sulawesi Region, N & C Maluku.

Foodplants.–– Boehmeria, Debregeasia, Girardinia, Oreocnide, Pipturus (Urticaceae).
Igarashi & Fukuda (1997) illustrate all life stages (Malaya).
–– *S. hippoclus clausus Fruhstorfer, 1904
Range.–– Sulawesi (N, C), Buton, Kabaena, Kep. Togian.
–– *S. hippoclus confluens Fruhstorfer, 1896
–– *S. hippoclus centho Fruhstorfer, 1904
Range.–– Kep. Banggai (Peleng), Kep Sula (Mangole, Sanana).
*S. platena Staudinger, 1896

*S. hippalus Felder & Felder, 1867

(Pl. 14, figs 7, 11)
*S. intricata Fruhstorfer, 1897

(Pl. 14, fig. 6 — Fancy Jester)
Vanessa Fabricius, 1807

(admirals, painted ladies — Pl. 14, fig. 10)
Range (1+2+5+6+7).–– Generally regarded as “cosmopolitan”, but not recorded

from Maluku, and only recently positively recorded from Borneo (see below). This
extremely familiar group of butterflies, which includes a total of 13 species divisible
amongst three subgenera, is represented on Sulawesi by a single endemic restricted to
Mt Lompobatang.
Foodplants.–– Apiaceae, Asteraceae, Balsaminaceae, Boraginaceae, Cannabidaceae,
Chenopodiaceae, Fabaceae, Geraniaceae, Lamiaceae, Malvaceae, Oleaceae, Salicaceae,
Scrophulariaceae, Smilacaceae, Tiliaceae, Ulmaceae, Urticaceae.
Key works.–– Field (1971), Tsukada (1985), Teshirogi (1990).
Vanessa (Vanessa) Fabricius, 1807
Range.–– North and Central America, Hawaii, Palaearctic Region, Oriental Region,
including the Philippines (Treadaway, in litt.), Sulawesi, and the Lesser Sunda
Islands; the subgenus does not occur in Maluku or further east into New Guinea, and
is only recently confirmed for Borneo: V. cardui Linnaeus was mapped for Borneo by
Tsukada (1985: 302), but not listed by Field (1971) or Otsuka (1988), nor is there any
authentic material in BMNH; Otsuka (1991), however, has now positively recorded it
from West Kalimantan.
Foodplants.–– Asteraceae (Ambrosia, Ammobium, Bracteantha, Carduus, Chrysocep-
halum, Cirsium, Helichrysum, Gnaphalium, Rhodanthe), Cannabidaceae (Humulus),
Lamiaceae (Braby, 2000), Malvaceae (Braby, 2000), Salicaceae (Populus, Salix),
Tiliaceae (Corchorus), Ulmaceae (Ulmus), Urticaceae (Boehmeria, Girardinia, Neraudia,

Parietaria, Pipturus, Soleirolia, Touchardia, Urera, Urtica).
*V. (V.) buana Fruhstorfer, 1898

(Lompobatang Lady — Pl. 14, fig. 10)
Kaniska Moore, 1899

(admirals — Pl. 14, fig. 3)
Range (2+6+7).–– Sri Lanka, India, Indo-China, China, Korea, Japan, Malay Penin-
sula, Sumatra, Java, Borneo, Philippines (Luzon, Mindoro, Panay and Mindanao only:
Treadaway, 1995), Sulawesi. This beautiful monobasic genus has often been conside-
red closely related to the Holarctic Polygonia and Nymphalis, but Nakanishi (1988), Tes-
hirogi (1990), Yoshimoto (2001) and Nylin et al. (2001) all demonstrate that, although
close, it is sufficiently distinct to justify continuing separation.
Foodplants.–– ?Dioscoreaceae, Liliaceae, Smilacaceae. Teshirogi (1990) (Japan) and
Bascombe et al. (1999) (Hong Kong) illustrate all life stages.
Key works.–– Tsukada (1985), Teshirogi (1990), Corbet & Pendlebury (1992).
K. canace Linnaeus, 1763

(Blue Admiral — Pl. 14, fig. 3)
Range (2+6+7).–– as genus.
Foodplants.–– ?Dioscoreaceae; Lilium, Streptopus, Tricyrtis (Liliaceae); Heterosmilax,
Smilax (Smilacaceae).
–– *K. canace muscosa Tsukada & Nishiyama, 1979
Kallimini Doherty, 1886

(pansies, buckeyes, egg-flies, leafwings — Pl. 14, figs 2, 4, 8, 9, 12)
Range.–– A mainly pantropical group, numbering well over 100 species. Five of
the approximately 16 genera occur in the Sulawesi Region.
Foodplants.–– Largely as subfamily.
Junonia Hübner, 1819

(pansies, soldiers, buckeyes — Pl. 14, fig. 4)
Range (W).–– Cosmopolitan, except for western Palaearctic.

The nominal genera Junonia and Precis Hübner, together up to 40 or more species,
are seen as closely related, yet separate genera by many authors, based largely on dif-
ferences in the male genitalia. Van Son (1979) strongly advocated treating them as no
more than subgenera. However, a recent analysis based on one mitochondrial and
two nuclear genes (COI, wingless and EF1α), although confirming the monophyly of
the two genera, strongly indicates that they are not sister to each other, Precis being
sister to Hypolimnas, while Junonia is sister to a group of three other, African genera
(Wahlberg, pers. comm.). Precis is restricted to Africa. Five species of Junonia occur on
Sulawesi.
Foodplants.–– Mainly Acanthaceae, Lamiaceae, Onagraceae, Poaceae, Scrophula-
riaceae, Verbenaceae, Violaceae.
Key works.–– Common & Waterhouse (1981), Tsukada (1985), Teshirogi (1990),
Corbet & Pendlebury (1992).
J. hedonia Linnaeus, 1764

(Brown Soldier, Chocolate Argus)
Range (W).–– Malay Peninsula, Sumatra, Java, western Lesser Sunda Islands, Bor-
neo, Palawan, Philippines, Sulawesi Region, N & C Maluku, New Guinea, Solomon
Islands, Australia.
Foodplants.–– Blechum, Hemigraphis, Hygrophila, Ruellia (Acanthaceae), Sida (Mal-
vaceae: Parsons, 1999). Parsons (1999) illustrates the pupa (Papua New Guinea). Braby
(2000) describes life cycle and behaviour.
–– *J. hedonia intermedia Felder & Felder, 1867 (= permagna Martin, 1920)
Range.–– Sulawesi, Kep. Sangihe (Siao), Salayar, Kabaena, Buton, Kep. Banggai
(Peleng).
–– J. hedonia ida Cramer, 1775
Range.–– Malay Peninsula, Sumatra, Java, Bali, Bawean, Borneo, Palawan, Philip-
pines, Kep. Talaud (Kaburuang, Karakelong, Salebabu), Kep. Sangihe (Sangihe).
–– *J. hedonia teurnia Fruhstorfer, 1912
Range.–– Kep Sula (Mangole, Sanana).
J. atlites Linnaeus, 1763

(Grey Pansy)
Range (W).–– Sri Lanka, India, Indo-China, China, Malay Peninsula, Sumatra,
Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi, Kep. Banggai, N
& C Maluku.
Foodplants.–– Asteracantha, Barleria, Blechum (in captivity: Igarashi & Fukuda,
1997), Hygrophila, Justicia, Nelsonia, Pseuderanthemum, Strobilanthes (Acanthaceae);
Achyranthes, Alternanthera (Amaranthaceae); Oryza (Poaceae); Lindernia (Scrophula-
riaceae); Phyla (Verbenaceae; in captivity). Igarashi & Fukuda (1997) illustrate all life
stages (Philippines).
–– *J. atlites acera Fruhstorfer, 1912
J. almana Linnaeus, 1758

(Peacock Pansy)
Range (1+2+5+6+7).–– Sri Lanka, India, Indo-China, China, Ryukyu Islands,
Malay Peninsula, Sumatra, Java, Lesser Sunda Islands, Borneo (Otsuka, 1991), Pala-
wan, Philippines, Sulawesi.
Foodplants.–– Acanthus, Asteracantha, Barleria, Blechum, Hemigraphis, Hygrophila,
Ruellia, Strobilanthes (Acanthaceae); Alternanthera (Amaranthaceae); Mimosa (Fabace-
ae); Gloxinia (Gesneriaceae); Osbeckia (Melastomataceae); Ludwigia (Onagraceae); Plan-
tago (Plantaginaceae); Antirrhinum, Bonnaya, Ilysanthes, Lindernia, Mimulus (Scrophula-

riaceae); Lippia, Phyla, ?Stachytarpheta (Verbenaceae). Teshirogi (1990) (Japan) and Iga-
rashi & Fukuda (1997) (Malaya) illustrate all life stages, as do Bascombe et al. (1999)
(Hong Kong).
–– *J. almana battana Fruhstorfer, 1906
Range.–– Sulawesi (C, S), Salayar, Buton, Kep. Tukangbesi (Kaledupa).
J. erigone Cramer, 1779

(Northern Argus)
(Pl. 14, fig. 4)
Range (3+4+5+6).–– Java, Lesser Sunda Islands, Sulawesi Region, N & C Maluku,
New Guinea, just reaching Wessel Islands, northern Australia (Braby, 2000).
–– J. erigone gardineri Fruhstorfer, 1902
Range.–– Sulawesi (C, S), Salayar, Buton, Kabaena, Kep. Tukangbesi (Tomea), cen-
tral Maluku.
J. timorensis Wallace, 1869

Range (P).–– Lesser Sunda Islands, Kalao.
–– *J. timorensis kucil Tsukada & Kaneko, 1985
Range.–– Kalao.
J. orithya Linnaeus, 1758

(Blue Pansy, Blue Argus)
Range (W).–– Afrotropical Region, Sri Lanka, southern India, northern India, Indo-
China, China, Malay Peninsula, Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan,
Philippines, Sulawesi Region, N & C Maluku, New Guinea region, Australia.
Foodplants.–– Acanthus, Asystasia, Barleria, Brunoniella, Hygrophila, Hypoestes, Justi-
cia, ?Lepidagathis, Pseuderanthemum , Rostellularia (Acanthaceae); Ipomoea (Convolvul-
aceae); Englerastrum, Plectranthus (Lamiaceae); Plantago (Plantaginaceae); Angelonia,
Antirrhinum, Buchnera, Misopates, Scrophularia, Striga (Scrophulariaceae); Thunbergia
(Thunbergiaceae); Lippia, Phyla (Verbenaceae); Viola (Violaceae). Teshirogi (1990)
(Japan) and Igarashi & Fukuda (1997) (Malaya) illustrate all life stages, as do Bascom-
be et al. (1999) (Hong Kong).
–– *J. orithya kontinentalis Martin, 1920
–– J. orithya celebensis Staudinger, 1888
Range.–– Sulawesi (C, S), Muna. Otsuka (1991) considers that material from Balik-
papan, eastern Kalimantan, also belongs to this subspecies.
–– *J. orithya saleyra Fruhstorfer, 1912
–– J. orithya kuehni Fruhstorfer, 1904
Range.–– Lesser Sunda Islands, Kalao, Kep. Tukangbesi (Kaledupa, Tomea, Bin-
ongko).
–– J. orithya orthosia Godart, 1823
Range.–– Kep. Sula (Sanana), central Maluku.
Yoma Doherty, 1886

(lurchers — Pl. 14, fig. 8)
Range (W).–– Burma, Indo-China, southern China, Malay Peninsula, Java, Lesser
Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region, N & C Maluku, New
Guinea region, Solomon Islands, northern Australia, Vanuata and New Caledonia.
Two species, apparently sympatric in parts of New Guinea (Parsons, 1999).
Foodplants.–– Acanthaceae.
Key works.–– Common & Waterhouse (1981), Tsukada (1985), Parsons (1999).
Y. sabina Cramer, 1780

(The Lurcher, Australian Lurcher — Pl. 14, fig. 8)
Range (W).–– Burma, Indo-China, southern China, Malay Peninsula, Java, Lesser
Guinea, northern Australia, Vanuata and New caledonia.
Foodplants.–– Dipteracanthus, Hemigraphis (Parsons, 1999), Ruellia, also Blechum
and Glendarussa in captivity (all Acanthaceae); Igarashi & Fukuda (2000) illustrate all
life stages (Maluku).
–– *Y. sabina nimbus Tsukada, 1985
Range.–– Sulawesi, Muna, Kalao, Kep. Tukangbesi (Kaledupa), Kep. Togian
(Waleabahi), Kep. Banggai (Peleng), Kep. Sula (Sanana).
–– *Y. sabina magnus Tsukada, 1985
Range.–– Kep. Talaud (Maburuan).
Rhinopalpa Felder & Felder, 1860

(wizards — Pl. 14, fig. 9)
Range (2+6+7).–– Assam, Thailand, Malay Peninsula, Sumatra, Java, Bali, Borneo,
Philippines (excluding Palawan), Sulawesi (monobasic).
Foodplants.–– Cecropiaceae, Urticaceae.
R. polynice Cramer, 1779

(The Wizard — Pl. 14, fig. 9)
Foodplants.–– Poikilospermum (Cecropiaceae); Conocephalus, Dendrocnide, Poikilos-
permum (Urticaceae). Igarashi & Fukuda (1997) illustrate all life stages (Philippines).
–– *R. polynice megalonice Felder & Felder, 1867
Hypolimnas Hübner, 1819

(diadems, egg-flies — Pl. 14, fig. 12)
Range (W).–– Palaeotropics, with slight extension into Neotropical Region. A

genus of about 30 species, some half of which occur in the Indo-Australian tropics.
Only three occur in Malaysia, whereas seven are recorded from the Sulawesi Region.
Foodplants.–– Acanthaceae, Amaranthaceae, Arecaceae, Asclepiadaceae, Asterace-

ae, Commelinaceae, Convolvulaceae, Crassulaceae, Fabaceae, Lamiaceae, Malvaceae,
Moraceae, Plantaginaceae, Polygonaceae, Portulacaceae, Rubiaceae, Tiliaceae, Urti-
caceae.
Key works.–– Vane-Wright et al. (1977), Common (1978), Common & Waterhouse
(1981), Tsukada (1985), Teshirogi (1990), Corbet & Pendlebury (1992).
*H. dimona Fruhstorfer, 1913

Range (L).–– Kep. Sula (Mangole).
*H. diomea Hewitson, 1861

Foodplants.–– Elatostema lineolatum (Urticaceae); see Teshirogi (2001), who also
illustrates egg, larva and pupa.
–– H. diomea diomea Hewitson, 1861
Range.–– Sulawesi (N, C, SE), Buton.
–– *H. diomea fraterna Wallace, 1869
–– *H. diomea sororia Hall, 1930
–– *H. diomea serica Tsukada, 1985
H. anomala Wallace, 1869

(Malayan Egg-fly, Crow Egg-fly — Pl. 14, fig. 12)
Range (1+2+5+6+7).–– Guam (Schreiner & Nafus, 1991), southern Japan, Ryukyu
Islands, southern China (rare: Bascombe et al., 1999), Taiwan, Malay Peninsula, Suma-
tra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region; recor-
ded twice from extreme northern Australia (Common & Waterhouse, 1981).
Foodplants.–– Claoxylon (Euphorbiaceae); Pipturus, Pouzolzia, Villebrunea (Urticace-
ae). Teshirogi (1990) illustrates the egg, first, second and fifth instars and the pupa
(Japan). Igarashi & Fukuda (1997) illustrate the larva and pupa (Philippines). Bascom-
be et al. (1999) illustrate the remarkable egg-guarding behaviour of this species
(Schreiner & Nafus, 1991).
–– *H. anomala stellata Fruhstorfer, 1912
Range.–– Sulawesi (N, C, S), Buton, Kabaena, Kep. Banggai (Peleng), Kep. Sula
(Sanana).
–– H. anomala anomala Wallace, 1869
Range.–– Malay Peninsula, Sumatra, Java, Borneo, Palawan, Philippines, Kep.
Sangihe.
H. antilope Cramer, 1777

Range (P).–– Kep. Talaud, Kep. Sangihe, N & C Maluku, New Guinea region,
Solomon Islands, New Caledonia, Fiji, Samoa.
Foodplants.–– Asystasia, Graptophyllum, Pseuderanthemum (Acanthaceae); Oreocnide,
Pipturus (Urticaceae: Parsons, 1999).
__ *H. antilope phalkes Fruhstorfer, 1908

Range.–– Kep. Talaud (Karakelong, Salebabu), Kep. Sangihe (Siao).
–– H. antilope antilope Cramer, 1777
Range.–– Kep. Sula (Mangole, Sanana), Maluku.
H. bolina Linnaeus, 1758

(Great Egg-fly, Varied Egg-fly)
Range (W).–– ?Kenya, Madagascar, Socotra, Sri Lanka, India, Indo-China, China,
Sulawesi Region, N & C Maluku, New Guinea, Australia, Pacific region.
Foodplants.–– Asystasia, Dipteracanthus, Justicia, Pseuderanthemum, Rostellularia,
Ruellia, Systasia (Acanthaceae); Alternanthera (Amaranthaceae); Eclipta, Synedrella
(Asteraceae); Commelina (Commelinaceae); Ipomoea, Merremia (Convolvulaceae); Des-
modium, Phaseolus, Vigna (Fabaceae); Perilla (Lamiaceae); Abutilon, Malvastrum, Sida
(Malvaceae); Ficus (Moraceae); Polygonum, Persicaria (Polygonaceae); Portulaca (Portu-
lacaceae); Richardia (Rubiaceae); Triumfetta (Tiliaceae); Boehmeria, Elatostema, Fleurya,
Laportea, Pipturus, Urtica (Urticaceae). Teshirogi (1990) (Japan) and Igarashi & Fukuda
(1997) (Philippines) illustrate all life stages, as do Bascombe et al. (1999) (Hong Kong).
–– H. bolina bolina Linnaeus, 1758 (= celebensis Fruhstorfer)
Range.–– Sumatra, Java, Lesser Sunda Islands, western Borneo, Sulawesi, Salayar,
Kabaena, Galla, Kep. Banggai (Peleng), Kep. Sula, northern Maluku, New Guinea
region, Solomon Islands, Australia, New Caledonia (distribution based on Fukuda &
Nicho, 1988).
Note.–– The “correct” subspecies is open to doubt; Parsons (1999) placed all New
Guinea populations as H. b. nerina Fabricius; Peggie et al. ( in litt.) applied the name H.
b. lisianassa Cramer to both northern and central Maluku populations.
–– *H. bolina gigas Oberthür, 1879
H. alimena Linnaeus, 1758

(Blue-banded Egg-fly)
Range (P).–– Eastern Lesser Sunda Islands, Kep. Talaud, ?Kep. Banggai, Kep. Sula,
Maluku, New Guinea region, Solomon Islands, New Caledonia, Australia.
Foodplants.–– Asystasia, Graptophyllum, Pseuderanthemum (Acanthaceae), Sida
(Malvaceae: Parsons, 1999), Pipturus (Urticaceae: Parsons, 1999). Braby (2000) descri-
bes eggs and larvae.
–– *H. alimena talauta Fruhstorfer, 1912
–– H. alimena alimena Linnaeus, 1758
Range.–– ?Kep. Banggai (Peleng; Nieuwenhuis, 1946), Kep. Tukangbesi (Wangi-
wangi and Lintea: Ohnishi & Sugimoto, 1998), Kep. Sula (Mangole), N & C Maluku,
New Guinea, Australia.
H. misippus Linnaeus, 1764

(Danaid Egg-fly)
Range (W).–– Antilles, northern South America, and throughout Afrotropical,
Oriental and Australian Regions, including Sulawesi, Muna and N & C Maluku.
Foodplants.–– Asystasia, Barlesia, Blepharis, Justicia, Pseuderanthemum, Ruellia (Aca-
nthaceae); Amaranthus (Amaranthaceae); Eleais (Arecaceae); Batatas (=Ipomoea) (Con-
volvulaceae); Abelmoschus, Abutilon, Gossypium, Hibiscus (Malvaceae); Ficus? (Morace-
ae); Plantago (Plantaginaceae); Portulaca, Talinum (Portulacaceae); Elatostema (Urticace-
ae). The life history was extensively described and early stages illustrated in Van Son
(1979). Teshirogi (1990) also illustrates all life stages.
Doleschallia Felder & Felder, 1860

(leafwings, autumn leaves — Pl. 14, fig. 2)
Range (W).–– Oriental and Australian Regions. A genus of about 10 species, most
richly developed in the New Guinea region. Sulawesi has a single representative.
Foodplants.–– Acanthaceae, Calycanthaceae, Fabaceae, Moraceae, ?Rubiaceae,
Urticaceae.
Key works.–– Common & Waterhouse (1981), Tsukada (1985), Corbet & Pendlebu-
ry (1992), Parsons (1999).
D. polibete Cramer, 1782

(Australian Leafwing — Pl. 14, fig. 2)
Range (3+4+5+6).–– Java, Lesser Sunda Islands, Sulawesi Region, N & C Maluku,
New Guinea (where it is locally sporadic: Parsons, 1999) and Australia (D. polibete aus-
tralis, Felder & Felder). Doleschallia butterflies from the Solomons, New Caledonia,
Vanuatu and Fiji formerly included in D. bisaltide or D. polibete, are now placed by
Parsons (1999) as a separate species, D. tongana Hopkins, 1927.
Foodplants.–– Asystasia, Graptophyllum, Pseuderanthemum, Strobilanthes (Acan-
thaceae).
–– *D. polibete celebensis Fruhstorfer, 1899
Range.–– Sulawesi, Kep. Talaud (Karakelong), Kep. Togian (Dolong), Salayar,
Buton, Galla, Kalao.
–– *D. polibete maturitas Tsukada, 1985
–– *D. polibete sulaensis Fruhstorfer, 1899
Danainae Boisduval, 1833

(milkweeds, crows, tigers, glasswings — Pl. 15, figs 6-10, Pl. 16)
Range.–– Cosmotropical, extending weakly into temperate Nearctic and Palaearc-

tic Regions. About 60 genera containing over 450 species divided into three tribes, one
of which is confined to the New Guinea region (Tellervini), and one to the Neotropics
(Ithomiini). The third is well represented in the Malay Archipelago, and is especially
diverse on Sulawesi.
Foodplants.–– Primarily Apocynaceae, Asclepiadaceae, Moraceae and Solanaceae.
Status.–– Several species are on the IUCN red list of threatened animals; their sta-
tus is given following Baillie & Groombridge (1996).
Key works.–– Morishita (1981), Ackery & Vane-Wright (1984), Kitching (1985),
Ackery (1987, 1988), Kitching et al. (1993), Ackery et al. (1999), Brower (2000).
Danaini Boisduval, 1833

(milkweeds, monarchs, tigers, crows, ghosts — Pl. 15, figs 6-10, Pl. 16)
Range.–– Cosmotropical, extending weakly into temperate Nearctic, Neotropical

and Palaearctic Regions. Twelve genera containing over 150 species divided into two
subtribes, both well represented in the Indo-Australian tropics.
Foodplants.–– Primarily Apocynaceae, Asclepiadaceae and Moraceae.
Key works.–– Morishita (1981), Ackery & Vane-Wright (1984), Ackery et al. (1999),
Brower (2000), Vane-Wright et al. (2002).
Danaina Boisduval, 1833

(milkweeds, monarchs, queens, tigers, wood nymphs — Pl. 15, figs 6-10)
Range.–– As subfamily. Two subgroups, both represented in Sulawesi, the first by

two of the four genera (Parantica and Ideopsis), the second by two of the three genera
(Danaus and Tirumala).
Foodplants.–– Primarily Apocynaceae and Asclepiadaceae.
Key works.–– Morishita (1981), Ackery & Vane-Wright (1984), Vane-Wright et al.
(2002).
Parantica Moore, 1880

(tigers — Pl. 15, fig. 10)
Range (W).–– Oriental, Australian and eastern Palaearctic Regions. A genus of

about 40 species, richly represented on Sulawesi by seven or even eight species. Four
(possibly five) of them belong to the entirely endemic kuekenthali-group (kuekenthali,
toxopei, dabrerai, hypowattan). The southern endemic sulewattan belongs to a small
group otherwise restricted to the Lesser Sunda Islands, while the Sulawesi Region
endemic, menadensis, is related to a large group of Indo-Philippine-Sundanian species.
The only local Parantica which extends outside the Sulawesi Region is cleona, found
also in Maluku; cleona forms a group with aspasia, found from Indo-China to Palawan
and Sumbawa.
Status.–– Five of the endemic species are on the IUCN red list of threatened ani-
mals (Baillie & Groombridge, 1996). Their status is given below.
Foodplants.–– Mainly Asclepiadaceae (Calotropis, Ceropegia, Cynanchum, Gymnema,
Hoya, Marsdenia, Metaplexis, Tylophora), Parsonsia (Apocynaceae: Parsons, 1999), Perip-
locaceae (Cryptolepis).
Key works.–– Morishita (1981), Ackery & Vane-Wright (1984), Vane-Wright et al.
(2002).
P. cleona Stoll, 1782

(Eastern Yellow Glassy Tiger)
Range (3+4).–– Sulawesi Region, N & C Maluku and Kep. Kai.
Foodplants.–– Gymnema tingens (Asclepiadaceae), recorded by Igarashi & Fukuda

(2000), who also illustrate all life stages.
–– *P. cleona luciplena Fruhstorfer, 1892
Range.–– Sulawesi, Salayar, Wowoni, Buton, Kep. Banggai (Peleng).
–– *P. cleona talautica Snellen, 1896
–– *P. cleona lucida Fruhstorfer, 1899
*P. sulewattan Fruhstorfer, 1896

(Bonthain Tiger — Pl. 15, fig. 10)
Status.–– endangered (Baillie & Groombridge, 1996).
*P. toxopei Nieuwenhuis, 1969

(Toxopeus’ Tiger)
Status.–– Vulnerable (Baillie & Groombridge, 1996).
*P. kuekenthali Pagenstecher, 1896

(Kuekenthal’s Tiger)
Status.–– Endangered (Baillie & Groombridge, 1996).
*P. dabrerai Miller & Miller, 1978

(d’Abrera’s Tiger)
*P. hypowattan Morishita, 1981

(Morishita’s Tiger)
*P. sp. (Zoological Museum, Amsterdam)

Range (E).–– Sulawesi (no more precise data). As noted by Ackery & Vane-Wright
(1984), a single female belonging to the Zoological Museum, Amsterdam, appears to
represent a fifth species of the kuekenthali-group.
*P. menadensis Moore, 1883

(Manado Tiger)
Status.–– Listed as threatened and rare in 1994 (Groombridge, 1994), but removed
from the red list in 1996 (Baillie & Groombridge, 1996).
–– *P. menadensis menadensis Moore, 1883
–– *P. menadensis niuwenhuisi Detani, 1983

–– *P. menadensis subsp. (Ackery & Vane-Wright, 1984)
Ideopsis Horsfield, 1858

(wood nymphs, tigers — Pl. 15, fig. 6)
Range (W).–– Sri Lanka, Indo-China, Malay Peninsula, Nicobar islands, Sumatra,
Java, Lesser Sunda Islands, Borneo, Philippines, Sulawesi Region, Maluku, New Gui-
nea eastwards to the Solomon Islands. A genus of ‘difficult’ butterflies still requiring
considerable work to arrive at meaningful species limits. The two species found in
Sulawesi are, however, extremely easy to separate from each other, representing the
two major clades (each with four currently recognised species) into which Ideopsis can
confidently be divided.
Foodplants.–– Mainly Apocynaceae, Asclepiadaceae, also Cardiopteridaceae,
?Piperaceae.
Key works.–– Morishita (1981), Ackery & Vane-Wright (1984).
I. juventa Cramer, 1777

(Young Tiger — Pl. 15, fig. 6)
Range (W).–– Malay Peninsula, Sumatra, Java, Lesser Sunda Islands, Borneo, Pala-
wan, Philippines, Sulawesi Region, N & C Maluku, western Lesser Sunda Islands and
New Guinea eastwards to the Solomon Islands.
Foodplants.–– Cynanchum, Gymnema, Heterostemma (Parsons, 1999), Pergularia,
Telosma (Asclepiadaceae); ?Piper (Piperaceae). Igarashi & Fukuda (2000) illustrate all
life stages (Malaya).
–– *I. juventa tontoliensis Fruhstorfer, 1897
–– *I. juventa tawaya Fruhstorfer, 1904
–– *I. juventa ultramontana Martin, 1914
–– *I. juventa ishma Butler, 1869
Range.–– Sulawesi (S, SE - Roos, 1993), Buton, Kabaena, Muna, Kep. Banggai
(Peleng).
–– *I. juventa lirungensis Fruhstorfer, 1899
Range.–– Kep. Talaud
–– *I. juventa satellitica Fruhstorfer, 1899
–– *I. juventa sequana Fruhstorfer, 1910
Range.–– Kep. Tukangbesi (Tomea, Binongko and Kaledupa).
–– *I. juventa homonyma Bryk, 1937
–– *I. juventa kallatia Fruhstorfer, 1904
Range.–– Kalao.
–– *I. juventa lycosura Fruhstorfer, 1910

Range.–– Bonerate.
–– *I. juventa sophonisbe Fruhstorfer, 1904
I. vitrea Blanchard, 1853

(Blanchard’s Wood Nymph)
Range (3+4).–– Sulawesi Region, N & C Maluku (apparently very rare in central
Maluku), New Guinea (Irian Jaya). The gaura complex, to which vitrea belongs, is dis-
tributed through Sundaland and Wallacea eastwards only to New Guinea (Vogelkop
and Biak); the complex is not represented in the Lesser Sunda Islands.
Foodplants.–– Cardiopteris moluccana (Cardiopteridaceae, or Icacinaceae) (also
Marsdenia tomentosa as substitute in captivity), recorded by Igarashi & Fukuda (2000),
who also illustrate all life stages.
–– *I. vitrea vitrea Blanchard, 1853
–– *I. vitrea arachosia Fruhstorfer, 1910
Range.–– Sulawesi (C, S), Buton.
–– *I. vitrea ribbei Röber, 1887
–– *I. vitrea iza Fruhstorfer, 1898
Range.–– Kep. Sula (Taliabu, Mangole, Sanana).
Tirumala Moore, 1880

(blue tigers — Pl. 15, fig. 7)
Range (1+2+4+5+6+7).–– Palaeotropics (but not recorded from N Maluku other

than Gebe). Another group of ‘difficult’ species; of the nine currently recognised, two
occur in Africa, the others in the Indo-Pacific. The genus is richly represented in Sula-
wesi by four species.
Foodplants.–– Mainly Apocynaceae, Asclepiadaceae.
T. choaspes Butler, 1886

(Sulawesi Blue Tiger — Pl. 15, fig. 7)
Range (R).–– ?extreme southern Philippines, Sulawesi Region.
Note.–– the southern Mindanao taxon tumanana Semper, also found on the near-
by Sarangani Islands, was attributed by Ackery & Vane-Wright (1984) to choaspes,
but it is placed by Morishita (1981) and by Treadaway (1995) as a disjunct race of
limniace; it should perhaps be regarded as a distinct species.
–– *T. choaspes choaspes Butler, 1886
–– *T. choaspes kalawara Martin, 1913
–– *T. choaspes subsp. (Roos, 1993)
–– *T. choaspes kroeseni Martin, 1910

Range.–– Buton.
–– *T. choaspes oxynthas Fruhstorfer, 1911
T. limniace Cramer, 1775

(The Blue Tiger)
Range (5+6).–– Throughout much of the Oriental Region, from Afghanistan to
China, Malay Peninsula, Java, ?Borneo, Lesser Sunda Islands, northern and central
Philippines (absent from Palawan and perhaps southern Philippines - but see note
under choaspes), and Sulawesi Region (but absent in north).
Foodplants.–– Holarrhena (Apocynaceae); Asclepias, Calotropis, Dregea, Heterostem-
ma, Hoya, Marsdenia, Tylophora (Asclepiadaceae); Crotalaria (Fabaceae); Epibaterium (=
Cocculus) (Menispermaceae). Ackery & Vane-Wright (1984) illustrate all life stages
(Hong Kong).
–– *T. limniace makassara Martin, 1910
–– *T. limniace bentenga Martin, 1910
–– *T. limniace subsp. (BMNH)
–– *T. limniace conjuncta Moore, 1883
Range.–– Kalao.
–– *T. limniace ino Butler, 1871
T. hamata Macleay, 1827

(Dark Blue Tiger, Blue Wanderer)
Range (1+2+4+5+6).–– Java, Lesser Sunda Islands, Philippines (apparently inclu-
ding Palawan: Treadaway, 1995), Hong Kong, Sulawesi Region, C Maluku, Gebe,
New Guinea region, Solomon Islands, Fiji, Tonga, Samoa, New Caledonia, Australia,
New Zealand.
Foodplants.–– Parsonsia (Apocynaceae); Cynanchum, Heterostemma, Hoya, Leichard-
tia?, Marsdenia, Secamone, Tylophora (Asclepiadaceae); Cryptostegia (Periplocaceae).
–– *T. hamata goana Martin, 1910
–– *T. hamata talautensis Talbot, 1943
–– *T. hamata arikata Fruhstorfer, 1910
T. ishmoides Moore, 1883

(Uncertain Blue Tiger)
Range (2+5+6).–– Java, Lesser Sunda Islands (Sumba), Philippines (absent from
Palawan), Sulawesi Region. The validity of the collective taxon remains open to doubt.
Foodplants.–– ?Parsonsia sp. (Apocynaceae).
–– *T. ishmoides ishmoides Moore, 1883

Range.–– Sulawesi, Bangka, Muna, Kep. Banggai.
Danaus Kluk, 1802

(monarchs, queens, tigers — Pl. 15, figs 8, 9)
Range (W).–– As subfamily. The 11 species are divided amongst three subgenera,
all represented in Sulawesi.
Foodplants.–– Mainly Asclepiadaceae.
Key works.–– Morishita (1981), Ackery & Vane-Wright (1984), Kitching et al. (1993).
Danaus (Danaus) Kluk, 1802
Range.–– As subfamily. The three species are all American but plexippus, the famous
Monarch butterfly, spread across the Atlantic and Pacific oceans during the 19th century
(Vane-Wright, 1993a); it was first recorded from Sulawesi by Semper (1873).
D. (D.) plexippus Linnaeus, 1758

(The Monarch, Milkweed, Wanderer, Black-veined Brown)
Range (3+4+5).–– As subfamily but absent from the Afrotropical Region (except
Mauritius), the Indian subcontinent, Malay Peninsula and islands of the Sunda Shelf
(formerly recorded in Borneo and the Philippines, but apparently extinct there now).
Foodplants.–– Apocynum? (Apocynaceae); Acerates, Araujia, Asclepias, Calotropis,
Gomphocarpus, Gonolobus, Marsdenia, Matelea, Oxypetalum, Stapelia (Asclepiadaceae);
Ipomoea (Convolvulaceae). Igarashi & Fukuda (1997) illustrate all life stages (Hawaii).
–– D. (D.) plexippus plexippus Linnaeus, 1758
Range.–– Northern and central America, Antilles, Azores, Canary Islands, Spain,
Mauritius, Réunion, Polynesia, Micronesia, New Caledonia, New Zealand, Solomon
Islands, Australia, New Guinea region, eastern Lesser Sunda Islands, N & C Maluku,
northern Sulawesi (Semper, 1873; Morishita, 1981), Philippines (material in BMNH;
apparently extinct), ?Borneo (probably extinct), Taiwan, and southern China (proba-
bly extinct: Bascombe et al., 1999).
Danaus (Salatura) Moore, 1880
Range.–– Oriental and Australian Regions. Four species, all represented on Sulawesi.
Foodplants.–– Asclepiadaceae.
D. (S.) ismare Cramer, 1780

(Wallacean Tiger)
–– *D. (S.) ismare alba Morishita, 1981
Range.–– Sulawesi (N), Kep. Sangihe (Sangihe, Siao), Kep. Talaud.
–– *D. (S.) ismare fulvus Ribbe, 1890
Range.–– Sulawesi (C, S), Kabaena.
–– *D. (S.) ismare subsp. (Ackery & Vane-Wright, 1984)

D. (S.) genutia Cramer, 1779

(Common Tiger, Orange Tiger, Dark Veined Tiger — Pl. 15, fig. 8)
Range (1+2+5+6+7).–– Sri Lanka, northern India, Indo-China, China, Malay Penin-
sula, Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi
Region, north-western Australia (absent from Maluku and New Guinea).
Foodplants.–– Asclepias, Ceropegia, Cynanchum, Graphistemma, Gymnema, Marsdenia,
Pergularia, Raphistemma, Sarcostemma, Stephanotis, Tylophora (Asclepiadaceae). Igarashi
& Fukuda (2000) illustrate all life stages (Laos), as do Ackery & Vane-Wright (1984)
and Bascombe et al. (Hong Kong).
–– *D. (S.) genutia leucoglene Felder & Felder, 1865
–– *D. (S.) genutia telmissus Fruhstorfer, 1910
Range.–– Buton, Kabaena, Muna.
–– *D. (S.) genutia tychius Fruhstorfer, 1910
–– *D. (S.) genutia subsp. (Ackery & Vane-Wright, 1984)
D. (S.) affinis Fabricius, 1775

(Malay Tiger, Swamp Tiger)
Range (3+4+5+6).–– Thailand, Malay Peninsula, Java, Lesser Sunda Islands, Phi-
lippines (Luzon, Mindoro and Marinduque only: Treadaway, 1995), Sulawesi Region,
N & C Maluku, New Guinea region, Solomon Islands, Australia, Vanuatu and New
Caledonia.
Foodplants.–– Cynanchum, Heterostemma (Parsons, 1999), Ischnostemma, Tylophora,
Vincetoxicum (Asclepiadaceae). Ackery & Vane-Wright (1984) illustrate the larva and
pupa (Australia).
–– *D. (S.) affinis fulgurata Butler, 1866
Range.–– Sulawesi, Kep. Sangihe (Siao), Bangka.
–– *D. (S.) affinis taruna Fruhstorfer, 1899
Range.–– Kep. Sangihe (Sangihe), Kep. Kawio (Marore).
–– *D. (S.) affinis affinoides Fruhstorfer, 1899
–– *D. (S.) affinis wentholti Martin, 1914
–– *D. (S.) affinis subsp. (Ackery & Vane-Wright, 1984)
Range.–– Kep. Tukangbesi (Binongko).
–– *D. (S.) affinis djampeana Van Eecke, 1915
–– *D. (S.) affinis hegesippinus Röber, 1891
–– *D. (S.) affinis subsp. (Ackery & Vane-Wright, 1984)
–– *D. (S.) affinis decentralis Fruhstorfer, 1899

Range.–– Kep. Banggai (Peleng), Kep. Sula (Mangole, Sanana).
D. (S.) melanippus Cramer, 1777

(White Tiger)
Range (1+2+5+6+7).–– North-eastern India, Indo-China, Malay Peninsula, Suma-
tra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi. The Sulawesi
races of melanippus are pale, largely white, like those found in the Philippines and Bor-
neo, quite unlike the dark orange or olivaceous races found in Java and the Lesser
Sunda Islands.
Foodplants.–– Gymnema, Tylophora (Asclepiadaceae). Igarashi & Fukuda (1997)
illustrate all life stages (Philippines).
–– *D. (S.) melanippus celebensis Staudinger, 1889
–– *D. (S.) melanippus meridionigra Martin, 1913
Danaus (Anosia) Hübner, 1816
Range.–– Nearctic, Neotropical, Afrotropical, Oriental and Australian Regions,

extending weakly into the Pacific and southern Palaearctic. Three of the four species are
exclusively American, while the fourth is very widely distributed in the Old World.
D. (A.) chrysippus Linnaeus, 1758

(Plain Tiger, African Queen, Lesser Wanderer — Pl. 15, fig. 9)
Range (W).–– Palaeotropics, westwards to the Cape Verde Islands, eastwards to
New Zealand, and northwards to the southern Palaearctic.
Foodplants.–– Asclepias, Aspidoglossum (=Schizoglossum), Brachystelma, Calotropis,
Caralluma, Ceropegia, Cynanchum, Gomphocarpus, Huernia, Ischnostemma, Kanahia, Lei-
chardtia, Leptadenia, Marsdenia, Metaplexis, Pachycarpus, Pentarrhinum, Pentatropis, Per-
gularia, Pleurostelma, Raphistemma, Rhyncharrhena, Sarcostemma, Schizoglossum, Secamo-
ne, Stathmostelma, Stapelia, Tylophora (Asclepiadaceae); Ipomoea (Convolvulaceae); Eup-
horbia (Euphorbiaceae), Periploca (Periplocaceae), Dyerophytum (Plumbaginaceae),
Erioglossum (Sapindaceae). Igarashi & Fukuda (1997) illustrate all life stages (Malaya),
as do Bascombe et al. (1999) (Hong Kong).
–– D. (A.) chrysippus chrysippus Linnaeus, 1758
Range.–– Mediterranean, NE Spain, North Africa (Tennent, 1996b), Middle East,
Indian subcontinent, China, Malay Peninsula, Sumatra, Borneo, Palawan, Philippines,
Kep. Sangihe, Kep. Talaud, Sulawesi (N).
–– *D. (A.) chrysippus gelderi Snellen, 1891
–– D. (A.) chrysippus bataviana Moore, 1883
Range.–– Java, Lesser Sunda Islands (to Flores), Salayar, Tanahjampea, Kalao,
Kep. Banggai (Peleng).
–– *D. (A.) chrysippus subsp. (Hopffer, 1874; Ackery & Vane-Wright, 1984)
–– *D. (A.) chrysippus subsp. (Ackery & Vane-Wright, 1984)

–– *D. (A.) chrysippus subsp. (Jurriaanse & Lindemans, 1920)
–– *D. (A.) chrysippus subsp. (Ackery & Vane-Wright, 1984)
–– D. (A.) chrysippus cratippus Felder, 1860
Range.–– ?Kep. Sula, N & C Maluku.
Euploeina Moore, 1880

(crows, tree nymphs, ghosts — Pl. 16)
Range.–– Cosmotropical, except for the whole of Africa and Madagascar. Two
subgroups, one in the New World (two genera), one in the Old (three genera). In latter
group the butterflies range from the Indian Ocean (Seychelles, Mascarenes) to the
Pacific. Two of these genera are represented on Sulawesi; the third (Protoploea) is
monobasic, and restricted to New Guinea.
Foodplants.–– Mainly Apocynaceae, Asclepiadaceae and Moraceae.
Euploea Fabricius, 1807

(crows — Pl. 16, fig. 1)
Range (W).–– Oriental, Australian and Pacific Regions, extending westwards to

include the Seychelles and Mascarene Islands. The largest genus of Danainae, with
more than 50 species, 14 of which occur in the Sulawesi Region. Cladistic resolution of
this potentially rich source of biogeographic data remains weak, and it is difficult to
conclude much from the Euploeas at present. The most remarkable Euploea species on
Sulawesi is E. magou, which appears to represent a stem lineage.
*E. magou Martin, 1912

(Magou Crow — Pl. 16, fig. 1)
E. sylvester Fabricius, 1793

(Two-brand Crow, Double-banded Black Crow)
Range (W).–– Sri Lanka, southern India, north-eastern India, Indo-China, Hong
Kong (rare: Bascombe et al., 1999), Malay Peninsula, Sumatra, Java, Lesser Sunda
Islands, Borneo, Palawan, Philippines, Sulawesi Region, N & C Maluku, New Guinea,
Australia.
Foodplants.–– Ichnocarpus, Parsonsia (Apocynaceae); Cynanchum, ?Gymnema (see
Braby, 2000), Hoya, Marsdenia (Asclepiadaceae); Ficus (Moraceae). Parsons (1999) illu-
strates the pupa (Papua New Guinea), and Braby (2000) describes eggs and larvae
(Australia).
–– *E. sylvester schlegelii Felder & Felder, 1865

Range.–– Sulawesi Region.
–– *E. sylvester glarang Martin, 1912
–– *E. sylvester subsp. (Ackery & Vane-Wright, 1984)
Range.–– Kabaena, Muna.
–– *E. sylvester agapa Fruhstorfer, 1911
E. phaenareta Schaller, 1785

(Giant Crow)
Range (W).–– Sri Lanka, Indo-China, Malay Peninsula, Sumatra, Java, Lesser
Guinea region, Solomon Islands.
Foodplants.–– Cerbera, Plumeria (Apocynaceae). Igarashi & Fukuda (1997) illustrate
all life stages (Palawan).
–– *E. phaenareta celebica Fruhstorfer, 1898
–– *E. phaenareta rolanda Fruhstorfer, 1904
Range.–– Sulawesi (C), Kep. Banggai (Peleng), Kep. Sula (Mangole).
–– *E. phaenareta subsp. (Ackery & Vane-Wright, 1984)
–– *E. phaenareta locupletior Fruhstorfer, 1899
–– *E. phaenareta subsp. (Ackery & Vane-Wright, 1984)
Range.–– Buton.
*E. configurata Felder & Felder, 1865

(Sulawesi Striped Blue Crow)
Range (E).–– Sulawesi (including SE: Roos, 1995).
Status.–– Listed as rare and threatened in 1994 (Groombridge, 1994), but removed
*E. eupator Hewitson, 1858

(Vanoort’s Crow)
Status.–– Listed as rare and threatened in 1994 (Groombridge, 1994), but removed
–– *E. eupator eupator Hewitson, 1858
Range.–– Sulawesi (N, C, S), Kep. Banggai (Peleng).
–– * E. eupator subsp. (Roos, 1995)
–– *E. eupator vanoorti Jurriaanse & Lindemans, 1920
–– *E. eupator thrasetes Fruhstorfer, 1911
–– *E. eupator sulaensis Joicey & Talbot, 1922

E. leucostictos Gmelin, 1790

(Orange-flash Crow)
Range (P).–– Kep. Talaud, Kep. Sangihe, Bunaken, N & C Maluku, New Guinea
region to New Caledonia and Fiji. Records of “leucostictos” from further west (e.g.,
Borneo: Otsuka, 1988) refer to E. eunice (see Ackery & Vane-Wright, 1984).
Foodplants.–– Ficus, Streblus (Moraceae). Parsons (1999) illustrates the larva and
pupa (Papua New Guinea).
–– *E. leucostictos lykeia Fruhstorfer, 1910
–– *E. leucostictos depuiseti Oberthür, 1879
–– *E. leucostictos subsp. (BMNH)
Range.–– Kep. Sangihe (Siao).
–– *E. leucostictos subsp. (BMNH)
Range.–– Bunaken (island near Manado, N. Sulawesi).
*E. westwoodii Felder & Felder, 1865

(Westwood’s King Crow)
–– *E. westwoodii meyeri Hopffer, 1874
Range.–– Sulawesi (N, C, SE - Roos, 1993).
–– *E. westwoodii westwoodii Felder & Felder, 1865
–– *E. westwoodii subsp. (BMNH)
Range.–– Bangka.
–– *E. westwoodii subsp. (BMNH)
Range.–– Buton.
–– *E. westwoodii leochares Fruhstorfer, 1910
Range.–– Salayar, Tanahjampea.
–– *E. westwoodii bangkaiensis Fruhstorfer, 1899
–– *E. westwoodii labreyi Moore, 1883
*E. cordelia Martin, 1912

(Cordelia Crow)
E. eleusina Cramer, 1780

(Vollenhov’s Crow)
Range (5+6).–– Pulo Laut (off southern Borneo), Kangean, Bawean, Java, western
Lesser Sunda Islands, Sulawesi Region.
Foodplants.–– Streblus asper (Moraceae) (recorded by Igarashi & Fukuda, 1997:

414). Igarashi & Fukuda (2000) illustrate all life stages.
–– *E. eleusina vollenhovii Felder & Felder, 1865
Range.–– Sulawesi (N, C, SE).
–– *E. eleusina anitra Fruhstorfer, 1910
–– *E. eleusina palata Fruhstorfer, 1910
–– *E. eleusina mniszechii Felder, 1859
–– *E. eleusina aganor Fruhstorfer, 1910
*E. hewitsonii Felder & Felder, 1865

(Hewitson’s Dwarf Crow)
–– *E. hewitsonii hewitsonii Felder & Felder, 1865
–– *E. hewitsonii reducta Jurriaanse, 1919
Range.–– Buton, Kabaena, Muna.
–– *E. hewitsonii mangolina Fruhstorfer, 1899
–– *E. hewitsonii besinensis Fruhstorfer, 1899
E. algea Godart, 1819

(Long-branded Crow, Mournful Crow, Algea Crow)
Range (1+3+4+5+6+7).–– Northern India, Indo-China, Malay Peninsula, Sumatra,
Java, Lesser Sunda Islands, Borneo, Palawan, Sulawesi Region, N & C Maluku, New
Guinea region, New Caledonia, Pacific islands, Australia. The validity of this taxon is
open to doubt (Ackery & Vane-Wright, 1984).
Foodplants.–– Ichnocarpus (Apocynaceae); Cynanchum (Asclepiadaceae); Ficus,
Streblus (Moraceae). Igarashi & Fukuda (2000) illustrate all life stages of the distinctive
Palau race. Parsons (1999) illustrates the pupa (Papua New Guinea).
–– *E. algea kirbyi Felder & Felder, 1865
–– *E. algea horsfieldii Felder & Felder, 1865
Range.–– Sulawesi (C, S, SE - Roos, 1993).
–– *E. algea bevagna Fruhstorfer, 1911
–– *E. algea talautensis Piepers & Snellen, 1896
–– *E. algea maura Hopffer, 1874
–– *E. algea laodikeia Fruhstorfer, 1910
–– *E. algea tombugensis Fruhstorfer, 1899

Range.–– Wowoni, Buton, Kabaena, Muna.
–– *E. algea wiskotti Röber, 1887
–– *E. algea corvina Fruhstorfer, 1898
E. core Cramer, 1780

(Common Crow, Common Indian Crow)
Range (P).–– One member of a group of five or more allopatric species (Vane-
Wright, 1993b.) widely but discontinuously distributed in the Oriental, Australian
and Pacific Regions. The complex is apparently unrepresented in Borneo, Philippi-
nes, Sulawesi, Maluku and New Guinea. The oldest named member, E. core Cramer
sensu stricto, is distributed from Sri Lanka through India to China, southwards
through the Malay Peninsula to Sumatra, Java and the Lesser Sundas islands (where
it may be being replaced by the common and well-known Australian Region mem-
ber of the complex, E. corinna Macleay), just penetrating the southern Sulawesi
Region in Kalao and Salayar. Other members of the complex occur in the Andamans
(E. andamanensis Atkinson), Nicobars (E. scherzeri Felder), Biak and Bismarck Archi-
pelago (E. charox Kirsch), with further splinter-species probably separable in the
Solomons area.
Foodplants.–– numerous genera in the Apocynaceae, Asclepiadaceae, Moraceae
and Periplocaceae. Igarashi & Fukuda (2000) illustrate all life stages (India).
–– *E. core bauermanni Röber, 1885
–– *E. core kalaona Fruhstorfer, 1898
Range.–– Kalao.
E. latifasciata Weymer, 1885

(Broad-banded Crow)
Range (3).–– Sulawesi Region, northern Maluku (including Obi).
–– *E. latifasciata latifasciata Weymer, 1885
Range.–– Sulawesi (see Roos, 1993).
–– *E. latifasciata hashimotoi Detani, 1983
E. redtenbacheri Felder & Felder, 1865

(Redtenbacher’s Crow)
Range (3+4).–– Southern Ryukyu Islands (Uesugi, 1984; requires confirmation),
Sulawesi, northern Maluku, central Maluku (Buru).
–– *E. redtenbacheri coracina Hopffer, 1874
–– *E. redtenbacheri redtenbacheri Felder & Felder, 1865
–– *E. redtenbacheri selayarensis Tsukada & Nishiyama, 1979
Idea Fabricius, 1807

(tree nymphs, ghosts, spectres, ideas, paper butterflies — Pl. 16, figs 2, 3)
Range (1+2+3+4+6+7).–– Sri Lanka, southern India, Burma, Malay Peninsula,

Sumatra, Java and Borneo east to New Guinea (Irian Jaya), including Philippines, Tai-
wan and Ryukyu Islands, but absent from Lesser Sunda Islands. A genus of 12 species
divided into two subgenera, only one of which occurs in Sulawesi.
Foodplants.–– Apocynaceae, Asclepiadaceae.
Key works.–– Morishita (1981), Ackery & Vane-Wright (1984), Kitching et al.
(1987), Okano (1985).
Idea (Idea) Fabricius, 1807
Range.–– As genus, except for Sri Lanka, southern India and northern Burma.
Seven species; of the two found on Sulawesi, one represents a stem lineage of the sub-
genus (tambusisiana). The other (blanchardii) is most closely related to a pair of species
from Maluku and the Vogelkop. A third species (leuconoe) is represented in the most
northerly part of the Sulawesi Region, and a fourth (idea) occurs on Kep. Sula.
*I. (I.) blanchardii Marchal, 1845

(Blanchard’s Ghost or Tree Nymph — Pl. 16, fig. 2)
Foodplants.–– Unknown in nature, but Igarashi & Fukuda (2000), who illustrate
all life stages, successfully raised this species on non-native Parsonsia (Apocynaceae).
–– *I. (I.) blanchardii blanchardii Marchal, 1845
Range.–– Sulawesi (N), Bangka, Kep. Sangihe (Siao).
–– *I. (I.) blanchardii marosiana Fruhstorfer, 1903
–– *I. (I.) blanchardii paluana Martin, 1914
–– *I. (I.) blanchardii subsp. (Roos, 1993)
–– *I. (I.) blanchardii garunda Fruhstorfer, 1910
–– *I. (I.) blanchardii munaensis Fruhstorfer, 1899
Range.–– Kabaena, Muna.
–– *I. (I.) blanchardii phlegeton Fruhstorfer, 1904
Range.–– Kep. Tukangbesi (Tolandono).
–– *I. (I.) blanchardii silayara Martin, 1914
–– *I. (I.) blanchardii djampeana Fruhstorfer, 1899
–– *I. (I.) blanchardii subsp. (Ackery & Vane-Wright, 1984)
Range.–– Kalao.
–– *I. (I.) blanchardii kuehni Röber, 1887
I. (I.) idea Linnaeus, 1763

(Linnaeus’ Idea)
Range (P).–– Kep. Sula, C. Maluku, Kep. Banda, Goram.
–– *I. (I.) idea sula de Nicéville, 1900
Range.–– Kep. Sula (Mangole, Sanana)
*I. (I.) tambusisiana Bedford Russell, 1981

(Bedford Russell’s Idea — Pl. 16, fig. 3)
–– *I. (I.) tambusisiana tambusisiana Bedford Russell, 1981
–– *I. (I.) tambusisiana hideoi Okano, 1985
I. (I.) leuconoe Erichson, 1834

(Siam Tree Nymph)
Range (P).–– Thailand, Malay Peninsula, Sumatra, ?Java, Borneo, Palawan, Philip-
pines, Taiwan, Ryukyu Islands, Kep. Talaud, Kep. Sangihe.
Foodplants.–– Parsonsia (Apocynaceae); Cynanchum, Dregea, Tylophora (Asclepia-
daceae). Igarashi & Fukuda (1997) illustrate all life stages (Philippines).
–– *I. (I.) leuconoe godmani Oberthür, 1879
–– *I. (I.). leuconoe esanga Fruhstorfer, 1898
Heliconiinae Swainson, 1822

(fritillaries, heliconians, acraeas, lacewings - Pl. 11, figs 3-8; Pl. 12, figs 1-4)
Range.–– Cosmopolitan, except New Zealand. Another large and widespread

group, it has been considered to comprise about 40 genera divided among four named
tribes, and an unnamed tribal assemblage. For a long period the exclusively American
and well-characterised tribe the Heliconiini (as prescribed by Michener, 1942) was
ranked as a full subfamily, but in recent years the group has been widened to embrace
the tropical Acraeini (often treated in the past as a separate subfamily also), the main-
ly north-temperate Argynnini and Boloriini, and an uncharacterised series of genera
including Cethosia, Vindula, Cupha, Phalanta and Yramea (Harvey, 1991). The Pardopsi-
ni are a monobasic African group, in the past included within the Acraeini, but now
considered of uncertain affinity. New insights into the classification of the Heliconii-
nae are given by Penz & Peggie (submitted), who propose to recognise three tribes,
but we cannot fully anticipate their results here.
Foodplants.–– Mainly Asteraceae, Flacourtiaceae, Passifloraceae, Urticaceae and
Violaceae.
Key works.–– Michener (1942), Warren (1944, 1955), Dos Passos & Grey (1945),
Brown (1981), Ackery (1988), Teshirogi (1990), Harvey (1991), Brower (2000), Penz &
Peggie (submitted).
unnamed tribal assemblage, incertae sedis

(Pl. 11, figs 5-8; Pl. 12, figs 1-3)
Range.–– An assemblage of about 16 genera, collectively worldwide in their distri-
bution, 7 of which are represented on Sulawesi. Harvey (1991) listed most of those
included in two groups as “subtribe uncertain”, to which the Boloriina must be
added.
Note added in proof.— If the scheme proposed by Penz & Peggie (submitted) is
accepted, then the next seven genera (Terinos to Phalanta) will be included in a named
subtribe of the Heliconiini.
Key works.–– Harvey (1991), Brower (2000).
Terinos Boisduval, 1836

(assyrians — Pl. 11, fig. 5)
Range (1+2+3+6+7).–– Oriental and Australian Regions, from Burma to the Bis-
marcks, but absent from Australia, C Maluku and Lesser Sundas. About eight species,
only one of which occurs on Sulawesi.
Foodplants.–– Euphorbiaceae (Antidesma), Flacourtiaceae (Casearia: Nuyda & Kita-
mura, 1993b; Homalium: Igarashi & Fukuda, 1997), Stilaginaceae, Violaceae (Rinorea:
Parsons, 1999).
Key works.–– Brooks (1930), Tsukada (1985), Corbet & Pendlebury (1992).
T. taxiles Hewitson, 1862

(Pl. 11, fig. 5)
Range (3).–– Sulawesi Region, N Maluku, New Guinea region. Parsons (1999) for-
mally treated the New Guinea and Bismarck components as distinct species, under
the names T. alurgis Godman & Salvin and T. maddelena Grose-Smith & Kirby, but con-
ceded that “alurgis may be better treated as a race of … abisares … known only from
Sulawesi … this may also be true of maddelena …” Here we treat them as a single spe-
cies; at the very least, it seems likely that the northern Maluku populations belong to
the same species-level taxon as the Sulawesi taxiles.
Foodplants.–– Rinorea (Violaceae: Parsons, 1999, for T. alurgis). Parsons (1999) also
illustrates the larva (Papua New Guinea).
–– *T. taxiles abisares Felder & Felder, 1867
Range.–– Sulawesi (N), Kep. Togian.
–– *T. taxiles poros Fruhstorfer, 1906
–– *T. taxiles banggaiensis Detani, 1983
–– *T. taxiles angurium Tsukada, 1985
T. clarissa Boisduval, 1836

(The Assyrian)
Range (P).–– Southern Burma, Thailand, Malay Peninsula, Sumatra, Java, Borneo,
Palawan, Philippines, Kep. Sangihe.
Foodplants.–– Homalium (Flacourtiaceae) and Rinorea (Violaceae), the former reco-

red by Igarashi & Fukuda (2000), who also illustrate all life stages (Palawan).
–– *T. clarissa ludmilla Staudinger, 1889
Vindula Hemming, 1934

(cruisers — Pl. 11, fig. 6)
Range (W).–– Oriental and Australian Regions, from Sri Lanka to N & C Maluku
and the Solomon Islands, including Australia. A small group of three or four species
(see Parsons, 1989, 1999), often difficult to separate; two occur on Sulawesi.
Foodplants.–– Passifloraceae.
Key works.–– Eliot (1956), Nieuwenhuis (1962), Common & Waterhouse (1981),
Tsukada (1985), Parsons (1989), Corbet & Pendlebury (1992).
V. erota Fabricius, 1793

(Common Cruiser — Pl. 11, fig. 6)
Range (1+6+7).–– Sri Lanka, India, Indo-China, China, Malay Peninsula, Sumatra,
Java, Borneo, Palawan, Sulawesi Region.
Note.–– Material currently identified as erota from the Sulawesi Region may repre-
sent a distinct endemic species, for which boetonensis would probably be the oldest
available name.
Foodplants.–– Adenia, Modecca, Passiflora (Passifloraceae). Igarashi & Fukuda
(1997) illustrate all life stages (Thailand).
–– *V. erota banta Eliot, 1956
–– *V. erota boetonensis Jurriaanse & Lindemans, 1920
Range.–– Buton.
–– *V. erota sulaensis Joicey & Talbot, 1924
V. dejone Erichson, 1834

(Erichson’s Cruiser)
Range (W).–– Thailand, Malay Peninsula, Sumatra, Java, Lesser Sunda Islands,
Borneo, Palawan, Philippines, Sulawesi Region, N & C Maluku.
Foodplants.–– Adenia, Passiflora (Passifloraceae). Igarashi & Fukuda (1997) illustra-
te eggs and pupae (Philippines).
–– *V. dejone celebensis Butler, 1883
Range.–– Sulawesi, Buton.
–– *V. dejone susanoo Tsukada, 1985
Range.–– Kep. Talaud (Karakelong, Kaburuang).
–– *V. dejone kabiana Fruhstorfer, 1912
–– V. dejone austrosundana Fruhstorfer, 1897
Range.–– Java, Lesser Sunda Islands, Kalao.
–– *V. dejone bushi Tsukada, 1985
–– *V. dejone satellitica Fruhstorfer, 1899

–– *V. dejone dioneia Fruhstorfer, 1912
Cupha Billberg, 1820

(rustics — Pl. 11, fig. 7)
Range (W).–– Oriental and Australian Regions, from Sri Lanka to New Guinea,
Solomon Islands and Australia. A genus of about ten species, three of which are found
in the Sulawesi Region.
Foodplants.–– Euphorbiaceae (Breynia: may be error according to Braby, 2000;
Glochidion), Flacourtiaceae (Flacourtia, Homalium, Scolopia, Xylosma), Rosaceae (Photi-
nia?), Salicaceae (Salix), Sapindaceae (Erioglossum, Lepisanthes).
Key works.–– Common & Waterhouse (1981), Tsukada (1985), Parsons (1989), Tes-
hirogi (1990), Corbet & Pendlebury (1992).
C. arias Felder, 1867

(Pl. 11, fig. 7)
Range (1+2).–– islands off coast NW Borneo (Mengalum, Mantanani), but not
recorded from main island (Otsuka, 1988), Palawan, Philippines, Sulawesi Region.
–– *C. arias celebensis Fruhstorfer, 1899
Range.–– Sulawesi, Kep. Banggai (Peleng; Nieuwenhuis, 1946).
–– *C. arias sangirica Fruhstorfer, 1912
Range.–– Kep. Sangihe (Sangihe, Siao), Kep. Talaud (Karakelong, Salebabu).
–– *C. arias muna Fruhstorfer, 1897
Range.–– Muna, Buton.
–– *C. arias subsp. (Rothschild Collection, BMNH)
Range.–– Kep Tukangbesi.
*C. maeonides Hewitson, 1859

–– *C. maeonides maeonides Hewitson, 1859 (including m. rovena Fruhstorfer)
Range.–– Sulawesi, Kep. Togian (Waleabahi, Dolong), Muna, Kabaena.
–– *C. maeonides butungensis Tsukada, 1985
Range.–– Buton.
–– *C. maeonides nigrico Tsukada, 1985
–– *C. maeonides maenada Grose Smith, 1898
C. crameri Felder, 1860

Range (P).–– Kalao, N & C Maluku, Gorong, Kep. Kai, western Irian Jaya.
–– *C. crameri kalaoensis Tsukada, 1985
Range.–– Kalao.
Algia Herrich-Schäffer, 1864 (= Paduca Moore, 1886: see Hemming, 1967)

(yeomen — Pl. 11, fig. 8)
Range (1+2+6+7).–– Oriental and Australian Regions, from Burma to New Guinea
(disjunct), being unknown from Maluku and the Lesser Sunda Islands. Three species,
the Sulawesi representative being endemic to the local region.
Foodplants.–– Unrecorded, but Richard Carver discovered the early stages in Papua
New Guinea, and they are thought to be similar to Cirrochroa (Parsons, 1999: 628).
Key works.–– Igarashi (1985), Tsukada (1985), Parsons (1989), Corbet & Pendle-
bury (1992).
A. fasciata Felder & Felder, 1860

(Branded Yeoman)
Range (P).–– Southern Burma, Thailand, Malay Peninsula, Sumatra, Java, Borneo,
Palawan, Philippines, Kep. Banggai, Kep. Sula.
–– *A. fasciata lautus Tsukada, 1985
–– *A. fasciata angustata Fruhstorfer, 1912
*A. satyrina Felder & Felder, 1867

(Pl. 11, fig. 8)
–– *A. satyrina satyrina Felder & Felder, 1867
–– *A. satyrina sibylla Röber, 1887
–– *A. satyrina subsp. (Roos, 1995)
–– *A. satyrina similliana Röber, 1887
Cirrochroa Doubleday, 1847

(yeomen — Pl. 12, fig. 1)
Range (1+2+3+5+6+7).–– Oriental and Australian Regions, from Sri lanka to N

Maluku, Flores and New Guinea. Of the 16-18 species, four regional endemics occur
on Sulawesi.
Foodplants.–– Flacourtiaceae (Flacourtia, Hydnocarpus).
Key works.–– Brooks (1930), Tsukada (1985), Parsons (1989), Corbet & Pendlebury
(1992), Roos (1996).
*C. thule Felder & Felder, 1860

(Pl. 12, fig. 1)
Range (R).–– Sulawesi, Kep. Togian (Dolong), Kep. Banggai (Peleng).
*C. semiramis Felder & Felder, 1867

*C. eremita Tsukada, 1985

*C. recondita Roos, 1996

Range (E).–– Sulawesi (SE).
Vagrans Hemming, 1934

(vagrants — Pl. 12, fig. 2)
Range (W).–– Oriental, Australian and Pacific Regions, from northern India to
Samoa and Tahiti. Two allopatric species according to Tsukada (1985), who is follo-
wed here (and by Treadaway, 1995), but many authors (e.g. Pinratana & Eliot, 1996;
Igarashi & Fukuda, 1997; Parsons, 1999) still recognise only one (egista Cramer, 1780).
Foodplants.–– Dilleniaceae (Dillenia: Igarashi & Fukuda, 1997), Flacourtiaceae (Fla-
courtia; Homalium: Braby, 2000; Xylosma: Bascombe et al., 1999).
Key works.–– Common & Waterhouse (1981), Tsukada (1985), Parsons (1989), Cor-
bet & Pendlebury (1992).
V. sinha Kollar, 1844

(The Vagrant — Pl. 12, fig. 2)
Range (1+2+5+6+7).–– Northern India, China, Indo-China, Malay Peninsula,
Sumatra, Java, Lesser Sunda Islands, Borneo, Palawan, Philippines, Sulawesi Region.
Foodplants.–– Flacourtia (Flacourtiaceae). Igarashi & Fukuda (1997) illustrate all
life stages (as egista, Malaya).
–– *V. sinha nupta Staudinger, 1889
Range.–– Sulawesi (N, C), Kep. Sula (Sanana).
Phalanta Horsfield, 1829

(leopards — Pl. 12, fig. 3)
Range (W).–– Afrotropical, Oriental, Australian and Pacific Regions. Five species,
with both the Indo-Australian species being found in Sulawesi (Parsons, 1989, recog-
nised only four, and Parsons, 1999, possibly five).
Foodplants.–– Celastraceae, Flacourtiaceae, Rubiaceae, Salicaceae, Smilacaceae,
Violaceae.
P. alcippe Stoll, 1782

(Small Leopard — Pl. 12, fig. 3)
Range (W).–– Sri Lanka, northern India, Indo-China, Malay Peninsula, Sumatra,
Maluku, New Guinea region, Solomon Islands, Samoa.
Foodplants.–– Flacourtia, Hydnocarpus (Flacourtiaceae); Salix (Salicaceae); Alsod-

eia, Melicytus, Rinorea (Violaceae). Igarashi & Fukuda (1997) illustrate all life stages
(Sulawesi).
–– *P. alcippe celebensis Wallace, 1869
Range.–– Sulawesi, Wowoni, Kep. Togian (Waleabahi).
–– *P. alcippe onyx Tsukada, 1985
Range.–– Kep. Talaud (Kaburuang).
–– P. alcippe aridus Tsukada, 1985
Range.–– Sumba, Kalao.
–– *P. alcippe handjahi Tsukada, 1985
–– *P. alcippe omarion Fruhstorfer, 1912
P. phalantha Drury, 1773

(Common Leopard, Spotted Rustic)
Range (1+2+5+6+7).–– Afrotropical Region, Sri Lanka, India, China, Indo-China,
southern Sulawesi Region, northern Australia.
Foodplants.–– Gymnosporia, Maytenus (Celastraceae); Petalostigma (Euphorbiaceae);
Aberia, Doryalis, Flacourtia, Scolopia, Trimeria, Xylosma (Flacourtiaceae); Canthium, Ixora
(Rubiaceae); Populus, Salix, Scolopia (Salicaceae); Smilax (Smilacaceae). Igarashi & Fuku-
da (1997) illustrate all life stages (India), as do Bascombe et al. (1999) (Hong Kong).
–– *P. phalantha sabulum Tsukada, 1985
Range.–– Sulawesi (S), Buton.
Argynnini Swainson, 1833

(fritillaries — Pl. 12, fig. 4)
Range.–– mainly north temperate. The approximately 100 species are divided into
about 12 genera, of which one occurs on Sulawesi.
Foodplants.–– Flacourtiaceae, Stilaginaceae, Violaceae.
Key works.–– Ackery (1988), Parsons (1989), Teshirogi (1990), Harvey (1991), Cor-
bet & Pendlebury (1992), Brower (2000).
Argyreus Scopoli, 1777

(The Indian Fritillary, Laced Fritillary — Pl. 12, fig. 4)
Range (5+6).–– Ethiopia, Sri Lanka, India, China, Japan, Indo-China, Malay Penin-
sula, Sumatra, Java, Bali, Lesser Sunda Islands (Flores), Philippines (Luzon, Mindoro),
Sulawesi, New Guinea, Australia. A monobasic but polytypic montane genus with a
most interesting distribution. Not recorded from Maluku (Samson, 1976).
Foodplants.–– Violaceae.
Key works.–– Warren (1955), Common & Waterhouse (1981), Tsukada (1985), Tes-
hirogi (1990), Corbet & Pendlebury (1992).
A. hyperbius Linnaeus, 1763

(The Indian Fritillary — Pl. 12, fig. 4)
Range (5+6).–– as genus.
Foodplants.–– Viola (Violaceae). Teshirogi (1990) (Japan) and Bascombe et al.
(1999) (Hong Kong) illustrate all life stages.
–– *hyperbius centralis Martin, 1913
Acraeini Boisduval, 1833

(acraeas, costers, lacewings — Pl. 11, figs 3, 4)
Range.–– Pantropical. Over 200 species, included in only three genera.

Foodplants.–– Mainly Asteraceae, Passifloraceae, Urticaceae.
Key works.–– Pierre (1984, 1987), Ackery (1988), Harvey (1991), Brower (2000).
Acraea Fabricius, 1807

(acraeas, costers — Pl. 11, fig. 3)
Range (3+4+5+6).–– Palaeotropics. Only weakly represented in the Indo-Pacific

region by about four or five species collectively occurring in India, China, Indo-China,
Burma, Sumatra, Java, Lesser Sunda Islands, Sulawesi, N & C Maluku, New Guinea,
Solomon Islands, Australia, New Caledonia, Samoa and Fiji, but the genus is not
known from the Malay Peninsula, Borneo or the Philippines. Two species are found in
Foodplants.–– Passifloraceae, Malvaceae, Violaceae, Urticaceae.
Key works.–– Common & Waterhouse (1981), Pierre (1984), Tsukada (1985), Cor-
A. andromacha Fabricius, 1775

(The Glasswing)
Range (P).–– Lesser Sunda Islands, Salayar, Kabia (E of Tanahjampea), Kep. Tuk-
angbesi (Tomea, Binongko), New Guinea, Solomon Islands (New Georgia), Australia,
New Caledonia, Samoa, Fiji.
Foodplants.–– Adenia, Passiflora (Passifloraceae); Hybanthus (Violaceae). Parsons
(1999) illustrates the larva (Papua New Guinea), and Braby (2000) describes larval
behaviour.
–– *A. andromacha indica Röber, 1885
Range.–– Salayar, Kabia, Kep. Tukangbesi (Tomea, Binongko).
A. moluccana Felder, 1860

(Eastern Mountain Coster — Pl. 11, fig. 3)
Range (3+4).–– Sulawesi Region, N & C Maluku, Papua New Guinea, Woodlark,
Bismarcks, Admiralty Islands, Solomon Islands.
–– *A. moluccana dohertyi Holland, 1891
Range.–– Sulawesi (N, C, S), Buton (material in ZSBS).
–– *A. moluccana parce Staudinger, 1896
Cethosia Fabricius, 1807

(lacewings — Pl. 11, fig. 4)
Range (W).–– Throughout the Indo-Australian Region, from Sri Lanka to China,
Lesser Sunda Islands, Sulawesi region, Maluku, New Guinea Region and northern
Australia. About 15 species (Parsons, 1989, 1999, recognises only 10), 4 of which have
been found in the Sulawesi Region.
Note added in proof.— In the scheme proposed by Penz & Peggie (submitted),
this genus is placed as a true heliconiine (tribe Heliconiini, subtribe Heliconiina).
Foodplants.–– Apocynaceae (Parsonsia: Igarashi & Fukuda, 1997), mainly Passiflo-
raceae (e.g. Adenia).
C. biblis Drury, 1773

(The Red Lacewing — Pl. 11, fig. 4)
Range (1+2+3+4+6+7).–– Northern India, Nepal, China, Indo-China, Malay Penin-
sula, Sumatra, western Java, Borneo, Palawan, Philippines, Sulawesi Region, N & C
Maluku.
Foodplants.–– Adenia, Balbas, Modecca, Passiflora (Passifloraceae). Igarashi & Fuku-
da (1997) illustrate all life stages (Nepal), as do Bascombe et al. (1999) (Hong Kong).
–– *C. biblis sarsina Fruhstorfer, 1912
Range.–– Sulawesi (N, C), Kep. Talaud (requires confirmation).
–– *C. biblis picta Felder & Felder, 1866
Range.–– Sulawesi (C, S), Kabaena, Muna, Buton.
–– *C. biblis togiana Fruhstorfer, 1902
*C. myrina Felder & Felder, 1867

(Violet Lacewing)
Foodplants.–– Raised on non-native Adenia (Passifloraceae) by Igarashi & Fukuda
(2000), who also illustrate the larva and pupa.
–– *C. myrina myrina Felder & Felder, 1867
–– *C. myrina melancholica Fruhstorfer, 1909
Range.–– Sulawesi (C), Kep. Togian (Waleabahi).
–– *C. myrina sarnada Fruhstorfer, 1912
–– *C. myrina vanbemmeleni Jurriaanse & Lindemans, 1918
Range.–– Buton.
–– *C. myrina ribbei Honrath, 1886
C. tambora Doherty, 1891

Range (P).–– Eastern Java, Bawean, Lesser Sunda Islands, Kalao.
–– *C. tambora atia Fruhstorfer, 1905
C. cydippe Linnaeus, 1763

(Eastern Red Lacewing)
Range (P).–– Kep. Sangihe, N & C Maluku, New Guinea region, northern Australia.
Foodplants.–– Adenia, Hollrungia (Passifloraceae).
–– *C. cydippe sangira Fruhstorfer, 1906
Range.–– Kep. Sangihe (requires confirmation).
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Received: 8.xi.2002
Accepted: 3.ii.2003
Edited: C. van Achterberg
Index to butterfly names
Species names are followed by the genus name, subspecies names by the name of the
species they are assigned to. References to figures on plates 1-16 are in italics, with
number of plate and number of figure separated by a slash; they are given for genus,
species and, if appropriate, subspecies.
aberrans (lysanias) ................ 194 albata (Parantica) .................... 25 andromacha (Acraea) ............ 236
abima (Zographetus) ........ 67, 2/6 albata (paulina) ..................... 110 andromache (Troides) .............. 18
Abisara ......................... 166, 8/37 albatus (Allotinus) ......... 116, 7/2 anemorcia (cymela) ................ 199
abisares (taxiles) .................... 230 albescens (daria) .................... 200 angelae (Nacaduba) ............... 143
acalle (Cephrenes) .............. 29, 74 albicilia (Halpe) ....................... 65 angulatum (Odontoptilum) ..........
acera (atlites) ......................... 209 albina (Appias) ...................... 109 ................................ 64, 1/12
Acerbas ........................... 70, 2/13 alcesta (Leptosia) ................... 103 angurium (taxiles) ................. 230
acetes (Arhopala) .................... 123 alcindor (polytes) ..................... 88 angusta (Nacaduba) ....... 142, 8/5
achates (Cyrestis) ..................... 27 alcippe (Phalanta) ........ 234, 12/3 angustata (fasciata) ............... 233
Achillides ................... 85, 4/5, 4/8 alecto (Jamides) ...................... 151 anitra (eleusina) .................... 226
acilia (Cyrestis) .......... 26, 27, 190 alfurus (Oriens) ............. 71, 2/16 anna (Lohora) ........................ 180
aconthea (Euthalia) ................ 202 algea (Euploea) ...................... 226 annulata (Arhopala) .............. 122
Acraea ................... 228, 235, 11/3 Algia ............................. 233, 11/8 anomala (Hypolymnias) ...............
Acraeini ........................ 229, 236 aliena (Taractrocera) ............... 72 ............................. 212, 14/12
acroleuca (Erionota) ................. 69 alimena (Hypolimnas) ........... 213 Anosia ........................... 222, 15/9
Acrophtalmia .. 31, 182, 10/12-13 alitaeus (Arhopala) ................ 123 antara (Pantoporia) ...... 197, 12/6
acuminata (nero) .................... 109 alitha (Eurema) .................. 98, 99 anthedon (Graphium) .... 9, 91, 92
Acytolepis ..................... 161, 8/29 Allotinus ................ 114, 115, 7/2 Anthene .................. 138, 139, 8/1
ada (Appias)............................ 107 almana (Junonia) ................... 209 antilope (Hypolimnas) ........... 212
adamantius (peranthus) ........... 86 alpheios (polytes) ..................... 88 antiphates (Graphium) ...... 93, 94
adamas (Pachliopta) ................. 84 alphenor (Papilio) .................... 88 antonio (Papilio) ...................... 18
Adoliadina ........................... 201 alphius (Polyura) ............. 26, 187 anysides (anysis) ................... 133
adorabilis (fasciatus) . 154, 8/18-19 alsulus (Famegana) ...... 154, 8/22 anysis (Dacalana) ......... 132, 7/18
aebutia (nina) ......................... 104 altijavana (rita) ...................... 146 Aoa .................... 18, 21, 112, 6/3
aeetes (Lexias) ............... 201, 13/2 aluta (Prosotas) ..................... 144 Apaturinae ........... 188, 192, 204
aegina (aegis) ......................... 108 alutina (aluta) ........................ 144 aphacus (fallax) ..................... 115
aegis (Appias) ........................ 108 alvenus (alecto) ...................... 151 Aphnaeini ............................ 130
aeropa (Lexias) ....................... 202 amabilis (Euthalia) ................ 203 aphrodite (Burara) ............ 55, 1/1
affinis (Aoa) .................... 112, 6/3 amanda (Euthalia) 202, 13/1, 13/6 apidanus (Flos) ............... 125, 7/8
affinis (Charaxes) .......... 185, 187 amarapta (lyncides) ............... 196 Appias 9, 23, 107, 108, 109, 6/13
affinis (Danaus) ............... 10, 221 Amathusia ...................... 169, 9/1 arachosia (vitrea) ................... 218
affinoides (affinis) .................. 221 Amathusiini ......................... 168 arachroa (celebica) ................. 199
agama (Caprona) ............ 64, 1/13 Amathuxidia .................. 170, 9/2 Araschnia ............................... 29
agamemnon (Graphium) .. 93, 5/3 Amauris ................................... 23 aratus (Jamides) ........... 150, 8/14
aganor (eleusina) ................... 226 Amblypodia .................. 126, 7/10 araxes (Arhopala) .................. 123
agapa (sylvester) .................... 224 Amblypodiini ...................... 126 arca (Flos) .............................. 125
agna (Pelopidas) ............. 77, 2/23 anana (kalelonda) .................. 184 archias (Taractrocera) ............. 28
agostina (Delias) .................... 106 anatha (europa) ...................... 176 arctofasciatus (eurypylus) ....... 92
agraria (Polyura) ............. 26, 187 Ancistroides ...................... 65, 2/3 arctous (Xois) ........................ 183
agricola (adamas) ..................... 84 ancus (Ypthima) .................... 184 arcuata (europa) ........... 176, 10/5
ahasverus (sataspes) ................ 87 ancyra (Catopyrops) ....... 146, 8/8 ardonia (Taractrocera) ....... 28, 71
aipytos (polyphontes) ............... 84 andamanensis (Euploea) ....... 227 area (ruficornis) ....................... 61
akirai (meges) ................... 96, 5/7 andersoni (Eurema) ................. 25 aretas (nynias) ....................... 183
alax (eryx) .................... 138, 7/24 andra (guttata) ........................ 76 argentea (Arhopala) ............... 122
alba (ismare) .......................... 220 androcles (Graphium) ......... 9, 94 argentiferus (schatzi) ............. 152
argeus (colon) .......................... 73 bambusae (Discophora) ......... 171 ............ 23, 24, 89, 228, 16/2
argiolus (Celastrina) ............. 162 banggaaiensis (leuce) ............. 182 blanda (Eurema) ...................... 99
Argynnini ..................... 229, 235 banggaiensis (mitisi) ............. 107 Bletogona 18, 21, 171, 10/2, 10/7
Argyreus ................... 235, 12/4-5 banggaiensis (taxiles) ............ 230 blumei (Papilio) ................ 85, 4/5
Arhopala ................. 121, 122, 7/7 banggaina (rahria) ................. 189 bochus(Jamides) ..................... 149
Arhopalini .............................. 121 bangkaia (festivus) ................. 151 boeticus (Lampides) ...... 153, 8/16
aria (Matapa) ........................... 28 bangkaiana (evelina) .............. 203 boetonensis (erota) ................. 231
Ariadne ................. 191, 12/10-11 bangkaianus (iapyx) .............. 131 boisduvali (Elodina) .............. 104
ariadne (Ariadne) .................. 191 bangkaiensis (bambusae) ....... 171 boisduvali (Miletus) .............. 117
ariae (battana) ........................ 106 bangkaiensis (sylvia) ............. 201 boisduvali (egnatia) ............... 104
arias (Cupha) ................ 232, 11/7 bangkaiensis (theda) .............. 130 boisduvalia (Melanitis) ................
aricles (Graphium) .................. 24 bangkaiensis (westwoodii) ..... 225 ........................ 30, 173, 10/3
aridus (alcippe) ...................... 235 bangkejana (scylla) ................ 100 bolina (Hypolimnas) .............. 213
arikata (hamata) .................... 219 banta (erota) ................. 231, 11/6 bolitissa (evelina) ................... 203
aristius (Udara) ..................... 161 bargylia (tritaea) ............ 102, 6/1 Boloriini ................................ 229
aristolochiae (Pachliopta) ........ 84 Bassarona ................... 203, 13/10 bonthainensis (hicetas) .......... 175
arsia (tominia) ....................... 100 bataviana (chrysippus) .......... 222 boopis (Chilades) .......... 164, 8/34
artaphernes (sataspes) ............. 87 bathycles (Graphium) .............. 24 bora (rita) ............................... 146
artemis (latona) ..................... 185 battana (Delias) ............. 105, 106 Borbo ............................... 76, 2/22
Artipe ..................... 17, 138, 7/24 battana (almana) ................... 210 borneana (bada) ....................... 76
ascalaphus (Papilio) ......... 89, 4/1 bauermanni (core) ................. 227 borneensis (hemina) ............. 15/2
ascalon (ascalaphus) ................ 89 Belenois ........................... 112, 6/7 bornemanni (cumaea) ............ 174
asema (scylla) ........................ 100 belinda (Melanitis) .................. 18 bouruana (leda) ..................... 172
asmara (Celaenorrhinus) .. 61, 1/6 belisama (Delias) ................... 106 bouruensis (oblongomaculatus) 81
aspasia (Cepora) .................... 112 belladonna (Delias) ................ 106 Brassolini .............................. 171
asterope (Ypthima) ................ 183 bellona (cognata) ................... 187 brassolis (Liphyra) ................. 114
athamas (Polyura) ........... 26, 187 benasu (Delias) ............. 106, 6/10 brevis (solon) ......................... 186
Athyma ................. 195, 196, 14/5 bentenga (limniace) ............... 219 brigitta (Eurema) ..................... 97
atia (tambora) ........................ 237 beraka (Caltoris) ...................... 78 bromus (Caltoris) .................... 78
atlites (Junonia) ..................... 209 berenice (Nacaduba) ....... 143, 8/4 bruijni (Tarattia) ................... 194
atrax (Melanitis) ................... 173 bernardus (Charaxes) ... 186, 11/1 brunnescens (tagalica) ........... 120
Atrophaneura ............................... beroe (Nacaduba) ................... 144 Buakraengius ......................... 163
........ 79, 83, 84, 3/3-4, 3/7-8 besina (janardana) ................. 178 buana (Vanessa) ......... 208, 14/10
attenuata (taminatus) ............. 57 besinensis (hewitsonii) .......... 226 bugiana (echerius) ................. 166
atymnus (Loxura) ........ 128, 7/13 bessa (luzonensis) .................... 72 Burara ................. 54, 55, 56, 1/1
atys (hewitsoni) ..................... 175 bettina (strigata) .................... 190 burgeri (khoda) ........................ 58
augiades (Cephrenes) ..... 74, 2/19 beturia (Halpe) ................. 65, 2/1 buruana (augiades) .................. 75
aurantiaca (panda) ................ 110 bevagna (algea) ...................... 226 bushi (dejone) ........................ 231
auriflua (harina) ...................... 97 bevani (Borbo) ................ 76, 2/22 butona (hicetas) ..................... 175
aurosa (zarinda ab.) .............. 109 Bia ....................................... 171 butongensis (aeetes) ............... 201
aurulenta (timnatha) ............. 111 Bibasis .......................... 54, 55, 56 butongensis (affinis) .............. 185
australis (celebensis) .............. 205 Biblidinae ..................... 188, 194 butongensis (macar) .............. 204
australis (polibete) ................. 214 Biblidini ........................ 188, 190 butungensis (dorcus) ............... 94
austrosundana (dejone) ......... 231 biblis (Cethosia) ............ 237, 11/4 butungensis (maeonides) ....... 232
avesta (Pseudergolis) .... 193, 13/9 bicolora (tephlis) .................... 123 butyrosa (Gandaca) .......... 96, 6/6
Azania ................................ 26, 27 Biini ....................................... 171 caelicola (hypolitus) ................. 80
azona (Acerbas) .............. 70, 2/13 bilinearis (tritaea) .................. 102 caeruleostriata (Hasora) .......... 58
azureus (pavana) ................... 142 Bindahara ..................... 135, 7/21 calathus (Lotongus) .......... 68, 2/8
bada (Parnara) ......................... 76 binongkoensis (tritaea) .......... 103 calauria (Nacaduba) .............. 144
Badamia ......................... 58, 1/3 biru (Jamides) ........................ 149 Caleta ...................... 147, 8/10-11
badoura (eulimene) ....... 197, 14/1 birumki (kuehni) .................... 132 caleta (Caleta) ......... 147, 8/10-11
badra (Hasora) ......................... 57 bisaltide (Deleschallia) .......... 214 Caltoris ........................... 78, 2/25
bakrii (aconthea) .................... 202 blanchardii (Idea) .......................... camenae (Udara) .......... 161, 8/28
cameria (Pratapa) .................. 132 celebica (Uranobothria) ......... 163 coelius (anthedon) ................... 92
camillus (Azania) .................... 27 celebicola (leda) ...................... 172 cognata (Polyura) .........................
canace (Kaniska) ........... 208, 14/3 celeno (Jamides) ..................... 149 .................. 26, 27, 187, 11/2
canuleia (narina) ................... 168 celinus (Miletus) ................... 117 Coladenia .................... 28, 62, 1/9
Caprona .......................... 64, 1/13 celis (plinius) ......................... 156 Coliadinae .............................. 96
cara (Monodontides) ............. 163 cellularis (hypolitus) ........ 80, 3/1 colon (Telicota) ........................ 73
cardui (Vanessa) .................... 207 celsina (Matapa) ....... 28, 70, 2/12 Colotis ............................ 101, 103
cassander (Cyrestis) .......... 26, 27 centaurus (Arhopala) ............ 124 comeda (elpis) ........................ 152
cassidyi (Rapala) ................... 136 centho (hippoclus) ................. 207 comodus (agamemnon) .... 93, 5/3
Castalius ......... 153, 154, 8/18-19 centralis (hyperbius) .............. 236 configurata (Euploea) ............ 224
castelnaui (Laringa) ... 192, 12/12 Cephrenes ........... 29, 30, 74, 2/19 confluens (hippoclus) ............ 207
Catochrysops ................ 152, 8/15 Cepora ........................... 110, 6/11 confusa (narada) ........... 126, 7/10
catoleucos (leos) ..................... 117 Cethosia ................ 229, 237, 11/4 conjuncta (limniace) .............. 219
Catophaga ................. 109, 6/13 chalcedonyx (Horaga) ............ 129 constantia (Melanitis) ........... 173
Catopsilia ...................... 100, 6/14 chamunda (Celaenorrhinus) .... 61 coracina (redtenbacheri) ........ 227
Catopyrops ..................... 146, 8/8 Charaxes ....................... 185, 11/1 corax (corvus) ........................ 155
catulus (solon) ....................... 186 Charaxinae ........................... 184 cordelia (Euploea) .................. 225
Cebrella .................................. 159 Charaxini .............................. 185 core (Euploea) ........................ 227
Celaenorrhinus ....... 60, 61, 1/5-6 charox (Euploea) .................... 227 corinna (Euploea) .................. 227
Celastrina ..................... 162, 8/30 Chelakina ............................... 159 corvina (algea) ....................... 227
celebensis (alcippe) ....... 235, 12/3 Cheritrini .............................. 129 corvus (Pithecops) ................. 155
celebensis (Ariadne) ... 191, 12/10 Chersonesia 18, 26, 27, 188, 13/5 crameri (Cupha) .................... 232
celebensis (arias) ........... 232, 11/7 Chilades ........................ 164, 8/34 cratippus (chrysippus) .......... 223
celebensis (bambusae) ............ 171 Chilasa .............................. 85, 4/2 criton (Troides) ........................ 81
celebensis (bolina) .................. 213 chione (Acrophtalmia) ........... 182 croesus (Ornithoptera) ............ 82
celebensis (Caleta) ................. 148 chionides (leuce) ......... 182, 10/13 cromyon (lajus) ..................... 165
celebensis (Cepora) ................ 111 chiron (Graphium) .................. 24 crowleyi (Parantica) ................ 25
celebensis (codrus) ............ 91, 5/6 chitone (menado) ................... 169 cumaea (Elymnias) ....... 174, 10/4
celebensis (criton) .............. 81, 82 Chliaria .................................. 133 Cupha ................... 229, 232, 11/7
celebensis (dejone) ................. 231 Choaspes ........................... 59, 1/4 Cupidopsis ............................. 140
celebensis (Eurema) ................. 99 choaspes (Tirumala) ..... 218, 15/7 Cupitha ........................ 64,66, 2/5
celebensis (feisthamelii) ........... 66 chromus (Hasora) .................... 56 Curetinae .............................. 119
celebensis (flegyas) ....... 166, 8/36 chrysanthis (Hypochrysops) . 121 Curetis ............................ 120, 7/6
celebensis (geoffroyi) .... 168, 15/5 chrysippus (Danaus) .... 222, 15/9 curius (Lamproptera) .............. 95
celebensis (glaucippe) ..... 102, 6/5 chrysoleuca (rosenbergi) ........ 107 cydippe (Cethosia) ................. 238
celebensis (Helcyra) ............... 204 chrysomelaena (Odina) .... 61, 1/7 cymela (Neptis) ..................... 199
celebensis (ida) ............. 199, 12/9 chrysozona (Cephrenes) .......... 74 Cyrestini ............................... 188
celebensis (kalelonda) ............ 184 cinnara (Borbo) ........................ 76 Cyrestis ....................... 18, 26, 27,
celebensis (melanippus) ......... 222 Cirrochroa .................... 233, 12/1 .............. 188, 189, 192, 13/7
celebensis (orithya) ................ 210 citatus (lymire) ...................... 195 cyrillus (Tajuria) .......... 131, 7/16
celebensis (phidippus) ............ 170 clarissa (Terinos) ................... 230 cyta (Jamides) ........................ 149
celebensis (polibete) ...... 214, 14/2 clathratus (Castalius) ............ 154 dabrerai (Parantica) 25, 215, 216
celebensis (rahria) ......... 189, 13/5 clausus (hippoclus) ................ 207 Dacalana ....................... 132, 7/18
celebensis (strabo) .................. 152 cleander (Arhopala) ............... 123 damar (Halpe) .......................... 65
celebensis (tagalica) ........ 120, 7/6 cleodus (Jamides) ................... 150 dan (Pseudocoladenia) ..... 62, 1/8
celebensis (thyonneus) . 190, 13/7 cleomenes (androcles) .............. 94 Danaina ................................ 215
celebica (echerius) .................. 166 cleona (Parantica) .................. 215 Danainae .............................. 214
celebica (Gerosis) ............ 62, 1/10 cleora (Deudorix) ................... 137 Danaini ................................. 215
celebica (Hypolycaena) .......... 135 cnejus (Euchrysops) ..... 164, 8/33 Danaus ........ 10, 215, 220, 15/8-9
celebica (Jamides) ................... 152 cocles (Cyrestis) ................. 26, 27 daria (Phaedyma) .................. 200
celebica (Neptis) ........... 198, 12/8 codrus (Graphium) ........... 91, 5/6 decentralis (affinis) ................ 222
celebica (phaenareta) ............. 224 Coeliadinae ............................ 54 decipiens (Lohora) ................. 180
celebica (quadripunctata) ........ 58 coelisparsus (Hypochrysops) . 121 dehanii (Polyura) ..................... 26
deianira (Lohora) ........... 180, 181 druna (Matapa) ....................... 28 Euploeina ............................. 223
deianirina (Lohora) ................ 180 Drupadia ...................... 129, 7/15 Eurema ................. 25, 30, 97, 6/2
dejone (Vindula) .................... 231 dubiosa (Prosotas) ................. 145 Euripus ......................... 205, 15/4
Delias .................... 18, 105, 6/10 dumoga (Logania) .................. 116 europa (Lethe) ............... 176, 10/5
deliciosa (Sancterila) .... 159, 8/27 duris (Acerbas) ........................ 71 eurygonia (Cepora) ................ 111
demetrius (schatzi) ................ 152 durvillei (Idea) ......................... 24 eurypylus (Graphium) .................
demoleus (Papilio) ............. 30, 90 eacus (dan) ....................... 62, 1/8 ......................... 9, 24, 25, 92
dentyris (hecabe) ...................... 98 echeilea (pseudosias) .............. 151 Eurytelina ............................. 190
depuiseti (leucostictos) .......... 225 echerius (Abisara) .................. 166 eutenia (lyncides) .................. 196
Deramas ......................... 119, 7/1 egista (Vagrans) .................... 234 Euthalia ....... 202, 203, 13/1, 13/6
dermoides (evelina) ...... 203, 13/3 egnatia (Elodina) ................... 104 evelina (Dophla) ........... 203, 13/3
deronda (puspa) ..................... 162 electra (Idea) ............................ 24 evemon (Graphium) ................ 24
detanii (leucippe) ................... 102 elegantia (euphrates) ............... 95 Everes ........................... 157, 8/24
deucalion (Graphium) ...... 95, 5/1 eleusina (Euploea) ................. 225 excellens (Chersonesia) ...... 18, 26
Deudorigini ......................... 135 elfeta (eridanus) .............. 122, 7/7 excellens (oedipodea) ............... 54
Deudorix ...................... 137, 7/23 eliana (berenice) ............. 143, 8/4 exclamationis (Badamia) .. 59, 1/3
dexamenus (Lohora) .............. 178 elioti (Jamides) ....................... 151 eximia (Cyrestis) ....... 26, 27, 190
dhanada (Celaenorrhinus) ....... 61 elioti (pia) ............................... 145 exophthalma (celebensis) ......... 99
diardi (Flos) ........................... 124 Eliotia .................................... 132 extremum (meyeri) .................. 93
Dichorragia .................. 192, 13/8 Eliotiana ................................ 132 fabulose (celebensis) ............... 205
dilecta (Udara) ....................... 160 ella (Prosotas)..........................145 fallax (Allotinus) ................... 115
dimona (Hypolimnas) ........... 212 Elodina ..................... 29, 104, 6/8 Famegana ..................... 154, 8/22
dina (hetaerus) ......................... 73 elpis (Jamides) ........................ 152 fasciata (Algia) ...................... 233
dinon (Lohora) ....................... 180 Elymnias ................ 18, 174, 10/4 fasciatus (Castalius) 154, 8/18-19
dioetas (Rapala) ..................... 136 Elymniina ............................. 174 faunia (tominia) ..................... 100
diomea (Hypolimnas) ............ 212 Elymniini .............................. 173 Faunis ................................... 168
dione (nina) ........................... 104 emesoides (Zemeros) .............. 166 feisthamelii (Notocrypta) ........ 66
dioneia (dejone) ...................... 232 emoloides (paraffinis) ............ 139 felixi (deucalion) ...................... 95
dionysiades (pomona) ............ 101 encelades (Graphium) .............. 95 fenestrata (mixta) ............. 57, 1/2
diotrophes (boisduvali) .......... 117 enipeus (Rapala) .................... 136 festivus (Jamides) .................. 151
Discolampa ..................... 148, 8/9 ennius (meges) ......................... 96 fettingi (Potanthus) ........ 73, 2/17
Discophora ....................... 18, 170 eperia (Cepora) ...................... 112 ficulnea (Celaenorrhinus) 60, 1/5
dispar (Elodina) ..................... 105 epijarbas (Deudorix) .... 137, 7/23 filia (timnatha) ............. 111, 6/11
distanti (Pirdana) .................... 28 epius (Spalgis) ................ 118, 7/5 filiola (timnatha) .................... 111
divona (Hestinalis) ....... 205, 15/3 eremita(Cirrochroa) ............... 234 flava (pomona) .............. 101, 6/14
dixoni (Atrophaneura) .. 83, 3/3-4 eridanus (Arhopala) ....... 122, 7/7 flavescens (Plastingia) ............. 68
djampeana (affinis) ................ 221 erigone (Junonia) .......... 210, 14/4 flegyas (Zemeros) ......... 166, 8/36
djampeana (alitha) ............. 98, 99 Erionota .......................... 69, 2/10 floresiana (lyncida) ................ 108
djampeana (aratus) ................ 150 erna (Lohora) ......................... 181 Flos ................................ 124, 7/8
djampeana (blanchardii) ........ 228 ernita (boisduvalia) ...... 173, 10/3 fluvialis (Castalius) ............... 154
dohertyi (Arhopala) ............... 122 erota (Vindula) ............. 231, 11/6 fora (Cepora) .......................... 112
dohertyi (mars) ...................... 186 erylus (Hypolycaena) ............ 134 fraterna (diomea) ................... 212
dohertyi (Troides) .............. 18, 82 eryx (Artipe) ................. 138, 7/24 fractilinea (Jamides) ............... 150
dohertyi (moluccana) ... 236, 11/3 esanga (leuconoe) ................... 229 Freyeria ................ 164, 165, 8/35
Doleschallia .................. 214, 14/2 espada (elpis) ......................... 152 fruhstorferi (blumei) ................ 86
dongala (luzonensis) ................ 72 ethion (Discolampa) .............. 148 fruhstorferi (menado) ............ 169
dongalae (celebensis) ............. 191 etsuzoi (Udara) ...................... 161 fukuyamai (ascalaphus) ........... 89
Dophla .......................... 203, 13/3 Euchrysops ................... 163, 8/33 fulgurata (affinis) .................. 221
dorcus (Graphium) ........... 94, 5/5 eulimene (Tacola) . 196, 197, 14/1 fuligo (Psolos) ................... 65, 2/2
dorimene (Delias) ............ 18, 106 eupator (Euploea) .................. 224 fulvus (ismare) ...................... 220
dorothea (umbretta) ............... 158 euphon (camenae) ......... 161, 8/28 fumata (phocides) ......... 135, 7/21
doson (Graphium) ................... 24 euphrates (Graphium) ............. 94 fumikoe (eurypylus) ................ 92
drakei (Sancterila) ................. 160 Euploea ................... 29, 223, 16/1 fumosa (evelina) .................... 203
furcatus (Choaspes) ................. 60 hegelochus (eulimene) ........... 197 hypnus (Lohora) ......... 181, 10/14
fuscula (fuligo) ................. 65, 2/2 hegesippinus (affinis) ............ 221 Hypochrysops ............... 18, 121
fuscus (Papilio) ........................ 87 Helcyra ......................... 204, 15/2 Hypolimnas .. 18, 209, 211, 14/12
gadames (nynias) ................... 183 helena (Semanga) .................. 125 hypolitus (Troides) ........... 80, 3/1
galaxia (Polyura) ................... 188 helena (Troides) .......... 80, 82, 3/5 Hypolycaena ......... 133, 134, 7/20
gamatius (erylus) .................. 134 helias (angulatum) ......... 64, 1/12 Hypolycaenini ..................... 133
Gandaca ............................ 96, 6/6 helicon (Ionolyce) ........... 147, 8/7 Hypothecla .................... 127, 7/12
Gangara ...................... 28, 68, 2/9 Heliconiinae ......................... 229 Hypotheclini ........................ 127
gardineri (erigone) ....... 210, 14/4 Heliconiini ........................... 229 hypowattan (Parantica) ................
garunda (blanchardii) ............ 228 hellada (cyta) ......................... 149 .......................... 25, 215, 216
gavalisi (Ypthima) ........ 184, 10/9 hemina (Helcyra) .......... 204, 15/2 iamos (plateni) ....................... 170
gedrosia (ariadne) .................. 191 hemixanthus (Choaspes) ......... 60 iapyx (Tajuria) ...................... 131
gelderi (chrysippus) ............... 222 hephaestus (helena) .......... 80, 3/5 ida (hedonia) .......................... 209
gellia (lyncida) ....................... 107 heracles (Cyrestis) ..... 26, 27, 189 ida (Neptis) ............. 18, 199, 12/9
genutia (Danaus) ......... 221, 15/8 hercules (Arhopala) ............... 123 Idea ............................... 4, 23, 24,
geoffroyi (Libythea) ...... 168, 15/5 hercules (Prusiana) ................. 75 25, 29, 30, 228, 228, 16/2-3
georgina (Delias) ................... 105 hermocinia (tritaea) ............... 103 idea (Idea) .................. 24, 89, 229
gerasa (aegis) ......................... 108 hermus (Nacaduba) ............... 142 Ideopsis ................. 215, 217, 15/6
Gerosis ............................ 62, 1/10 Hesperiidae ..................... 15, 32 iliona (solon) .......................... 186
gigas (bolina) ......................... 213 Hesperiinae ............................ 64 ilissus (Discolampa) ....... 148, 8/9
gigon (Papilio) ............ 18, 87, 4/7 Hesperioidea ......................... 31 illustris (tritaea) .................... 103
giscon (sipylus) ............ 135, 7/20 Hestia ....................................... 24 Ilma ........................... 21, 70, 2/11
glarang (sylvester) ................. 224 Hestina .................................. 205 iluska (Bibasis) ........................ 56
glaucippe (Hebomoia) ..... 102, 6/5 Hestinalis ..................... 205, 15/3 imitatrix (Lohora) ...... 181, 10/16
gnoma (trochylus) ................. 165 hetaerus (Potanthus) ............... 73 imperialis (Burara) .................. 55
goana (hamata) ...................... 219 hewitsoni (Elymnias) ............ 175 imperiosa (diardi) .................. 124
godmani (leuconoe) ............... 229 hewitsonii (Euploea) .............. 226 ina (brigitta) ............................ 97
gomata (Burara) ...................... 55 hicetas (Elymnias) ................. 174 incerta (Zethera) .... 23, 175, 10/6
gordion (eurypylus) ................. 92 hicetina (hicetas) .................... 175 indica (andromacha) .............. 236
gracilis (Prosotas) .................. 145 hideoi (tambusisiana) ... 229, 16/3 indrasari (Sinthusa) .............. 138
gradeniga (philippina) .. 162, 8/30 hiereia (daria) ........................ 200 inexpectata (theda) ................ 129
Graphiini ................................ 90 hima (apidamus) .................... 125 inexspectata (Bletogona) ..............
Graphium ..................................... Hiposcritia ........................... 109 ...................... 172, 10/2, 10/7
.... 9, 24, 90, 91, 93, 95, 5/1-6 hippalus (Symbrenthia) ................ inga (Lohora) ......................... 180
guttata (Parnara) .................... 76 .............. 29, 207, 14/7, 14/11 ino (limniace) ......................... 219
haasei (Lohora) ...................... 180 hippoclus (Symbrenthia) . 29, 206 ino (mimalon) ........................ 174
halesa (tominia) ..................... 100 hipponous (Papilio) ................. 87 inopinatus (Polyura) ....... 27, 187
haliphron (Troides) ............ 81, 82 hiraca (Erionota) ............ 69, 2/10 insularis (eurypylus) ............... 92
Halpe ................................ 64, 2/1 hiromii (lysanias) .................. 194 insularis (kuehni) .................... 75
halus (Jamides) ...................... 151 hombroni (Appias) ................. 108 insulicola (peranthus) ...... 86, 4/8
hamata (Tirumala) ................ 219 homonyma (juventa) ............. 217 intermedia (Chersonesia) ......... 26
handjahi (alcippe) .................. 235 honos (Hypothecla) ...... 127, 7/12 intermedia (hedonia) ............. 209
hannibal (solon) ..................... 186 Horaga .......................... 128, 7/14 intermedia (Matapa) ......... 28, 70
harina (Gandaca) ..................... 97 Horagini ............................... 128 intermedia (specularia) .......... 191
harisa (Burara) ........................ 55 horsfieldi (Mycalesis) ............ 178 intermedius (menado) ........... 169
harpalycus (nesimachus) ....... 193 horsfieldii (algea) ................... 226 intermedius (peranthus) .......... 86
hasdrubal (thrax) ..................... 69 hyela (Pirdana) .................. 28, 71 intricata (Symbrenthia) ................
hashimotoi (latifasciata) ........ 227 hylas (Neptis) ........................ 199 ......................... 29, 207, 14/6
Hasora .............................. 56, 1/2 hylax (Zizula) ............... 157, 8/23 Iolaini .................................... 130
hayashii (beroe) ...................... 144 hylecoetes (pyrrha) ................ 173 Ionolyce .......................... 147, 8/7
Hebomoia ........................ 101, 6/5 hyparete (Delias) ................... 106 Iraota ............................ 126, 7/11
hecabe (Eurema) ...................... 98 hyperbius (Argyreus) 236, 12/4-5 irena (Eurema) .................. 25, 99
hedonia (Junonia) .................. 209 hypermnestra (Idea) ................ 24 irmae (Cyrestis).........................26
irregularis (Arhopala) ........... 122 kirbyi (algea) .......................... 226 lesbia (pava) ............................. 73
irvina (Ilma) ................... 70, 2/11 klados (menado) ..................... 169 Lethe ........................... 176, 10/15
ishma (juventa) ...................... 217 kojimai (lycone) ..................... 196 Lethina .................................. 176
ishmoides (Tirumala) ............ 219 kolari (Monodontides) .. 163, 8/32 leuce (Acrophtalmia) .. 182, 10/13
ismare (Danaus) .................... 220 kontinentalis (orithya) ........... 210 leucippe (Hebomoia) .............. 102
ismene (Pirdana) ...... 28, 71, 2/14 kotzebuea (Pachliopta) ............. 84 leucoglene (genutia) ..... 221, 15/8
ithome (Appias) ..................... 108 kransi (paulinus) ................... 189 leuconoe (Idea) ................. 24, 229
Ithomiini ............................... 214 kransi (peranthus) ................... 86 leucospila (Hasora) .................. 58
itys (Mycalesis) .......... 177, 10/10 kroeseni (choaspes) ................ 219 leucostictos (Euploea) ............ 225
iudith (Cepora) ...................... 112 kucil (timorensis) ................... 210 lewara (eridanus) ................... 122
Ixias ........................ 101, 103, 5/4 kuehni (Atrophaneura) . 83, 3/7-8 lewara (Hypolycaena) ............ 134
iza (vitrea) ............................. 218 kuehni (blanchardii) .............. 228 lewari (aristius) ..................... 161
jalindra (Rachana) ................ 7/17 kuehni (Delias) ...................... 105 Lexias ............................ 201, 13/2
jalysus (mantra) .................... 131 kuehni (Flos) .......................... 125 libanius (demoleus) ................. 90
Jamides ......................... 148, 8/14 kuehni (orithya) ..................... 210 libnites ((Athyma) ........ 195, 14/5
janardana (Mycalesis) ........... 178 kuehni (Paruparo) ................. 132 Libythea ..................... 167, 15/5
jangala (Remelana) ...... 133, 7/19 kuehni (paulinus) .................. 189 Libytheinae .......................... 167
japetus (Tagiades) .................... 63 kuehni (perimale) ................... 111 licates (Anthene) ............ 140, 8/1
java (Belenois) ........ 112, 113, 6/7 kuehni (Prusiana) .......... 75, 2/20 lignea (Leptosia) ............. 104, 6/9
javanica (hyperbius) ......... 12/4-5 kuehni (puspa) ....................... 162 lilaea (Symbrenthia) ........ 29, 206
jobates (Cupidopsis) .............. 140 kuekenthali (Parantica) ................ liliputa (ida) ........................... 199
johnsoniana (rochana) .. 127, 7/11 ......................... 25, 215, 216 Limenitidina ........................ 194
jopas (Orsotriaena) ...... 177, 10/8 kurava (Nacaduba) ................ 143 Limenitidini ......... 188, 193, 194
jordani (Papilio) ........ 4, 89, 4/3-4 kurosawai (antiphates) ............ 94 limniace (Tirumala) ............... 219
junkoae (Ypthima) ................. 184 labotas (Bassarona) .... 203, 13/10 linga (phedima) ...................... 173
Junonia ......................... 208, 14/4 labreyi (westwoodii) .............. 225 LiphyraI ................................. 114
juventa (Ideopsis) ......... 217, 15/6 lacturnus (Everes) ........ 158, 8/24 Liphyrinae ............................ 112
kabiana (dejone) ..................... 231 lajus (Chilades) ...................... 164 Liphyrini .............................. 113
kalaoensis (antiphates) ............ 94 lalassis (perseus) .................... 178 lirungensis (juventa) ............. 217
kalaoensis (crameri) ............... 232 Lamasia ............................ 21, 196 locupletior (phaenareta) ........ 224
kalaomemnon (memnon) ......... 89 Lampides ...................... 153, 8/16 Logania ........................... 116, 7/3
kalaona (core) ......................... 227 Lamproptera ..................... 95, 5/7 Lohora . 18, 21, 30, 179, 10/15-16
kalaonicus (galaxia) ............... 188 Lampropterini ....................... 90 lombokiana (Eurema) .............. 25
kalawara (caleta) .................... 147 laodikeia (algea) ..................... 226 lompa (chrysozona) ................. 74
kalawara (choaspes) ...... 218, 15/7 Laringa ....................... 192, 12/12 longicornis (Ancistroides) 66, 2/3
kalawara (Hypolycaena) ........ 134 larymna (Tacola) ................... 196 longilinea (monticolus) ........... 91
kalawarus (alsulus) ............... 155 Lasippa ......................... 198, 12/7 longilineatus (monticolus) ...... 91
kalawarus (celeno) ................. 150 latefascia (Acerbas) .................. 70 lorquini (alitha) ....................... 99
kalelonda (Ypthima) .............. 184 latifasciata (Euploea) ............. 227 loryma (Ypthima) .................. 184
kalidupa (hecabe) ..................... 98 latimargo (hecabe) ................... 98 Losaria ........................ 79, 83, 3/6
kalidupa (ida) ......................... 199 latimargus (alecto) ................. 151 Lotongus ........................... 68, 2/8
kallatia (juventa) ................... 217 latona (Charaxes) .................. 185 loxius (Deudorix) .................. 137
Kallimini ............................... 208 lautus (fasciata) ..................... 233 Loxura .......................... 127, 7/13
Kaniska ................. 206, 208, 14/3 lavendularis (Celastrina) ....... 162 Loxurini ................................ 127
karsandra (Zizeeria) ..... 156, 8/20 laxmi (Coladenia) .................... 28 lubricans (Polytremis) ... 78, 2/24
karschi (lysanias) ................... 194 lebadea (Gangara) .................... 28 lucida (cleona) ....................... 216
kausambi (Abisara) ...... 167, 8/37 leda (Melanitis) ..................... 172 Luciini ................................... 121
kawazoei (Parnara) ........ 76, 2/21 leechi (Graphium) .................... 24 luciplena (cleona) .................. 216
kazueae (Delias) ..................... 106 leochares (westwoodii) ........... 225 ludmilla (clarissa) .................. 231
kazuyoe (celebensis) ............... 111 leos (Miletus) ................. 117, 7/4 lulu (alsulus) ........................ 8/22
kehelatha (Coladenia) . 28, 62, 1/9 Leptocircini ............................ 90 lunata (aratus) ............. 150, 8/14
khoda (Hasora) ........................ 58 Leptosia ........................... 103, 6/9 lunifer (fuscus) ........................ 88
kikuoi (Delias) ....................... 106 Leptotes ......................... 155, 8/17 luniger (alecto) ...................... 151
lutatia (lyncida) ..................... 107 marosiana (blanchardii) ........ 228 mniszechii (eleusina) ............. 226
lutea (Cyrestis) .................. 18, 26 mars (Charaxes) .................... 186 Moduza .......................... 194, 195
luzonensis (strabo) ................ 152 masae (Deramas) ................... 119 moeros (Pithecops) ................. 155
luzonensis (Taractrocera) ............. matanga (Cebrella) ................ 159 moestissima (Hasora) .............. 58
.............................. 28, 29, 71 Matapa ..................... 28, 70, 2/12 moluccana (Acraea) ...... 236, 11/3
luzonicus (cnejus) ................. 164 mathias (Pelopidas) ................. 77 Monodontides ............... 163, 8/32
Lycaenesthini .............. 138, 139 matinus (prusias) .................... 75 monticolus (Graphium) ... 91, 5/4
Lycaenidae ..................... 15, 113 maturitas (polibete) ............... 214 Morphinae ........................... 168
lycaenina (Anthene) .............. 139 maura (algea) ......................... 226 muna (arias) .......................... 232
lycaenolus (Anthene) ............. 139 maximus (Allotinus) ............. 115 munaensis (blanchardii) ........ 228
lycaste (lyncida) ..................... 108 maximus (leos) ............... 117, 7/4 munaensis (lymire) ............... 195
lyce (lavendularis) ................. 163 medus (Orsotriaena) ............. 177 munaensis (rosenbergi) ......... 107
lycone (Moduza) .................... 196 megakles (epijarbas) ..... 137, 7/23 munascalaphus (ascalaphus) ... 89
lyconides (lycone) .................. 196 megalonice (polynice) ... 211, 14/9 musa (Zethera) ...................... 175
lycosura (juventa) ................. 218 meges (Lamprotpera) ........ 95, 5/7 musashi (Charaxes) ............... 186
lydanus (cleodus) ................... 150 Megisba ........................ 158, 8/26 muscosa (canace) ................... 208
lykeia (leucostictos) ............... 225 mehavagga (Caltoris) ..... 78, 2/25 Mycalesina ........................... 176
lymire (Moduza) .................... 195 melancholica (myrina) ........... 237 mycalesis (Bletogona) ... 171, 10/1
lyncida (Appias) .................... 107 melanippus (Danaus) ............ 222 Mycalesis ........ 21, 177, 10/10-11
lyncides (Lamasia) ................. 196 Melanitini ............................. 171 Mynes .............................. 29, 206
lysanias (Tarattia) ................. 194 Melanitis .......... 18, 30, 172, 10/3 mynois (Mycalesis) .... 179, 10/11
macar (Rohana) ............ 204, 15/1 meliophila (hewitsoni) ........... 175 myrina (Cethosia) .................. 237
macareus (Graphium) ............. 93 melusina (Delias) .................. 106 Nacaduba .................... 141, 8/4-5
macassarensis (Allotinus) ..... 115 memnon (Papilio) .................... 89 naja (Plastingia) ...................... 67
madensis (Charaxes) ............. 186 menadensis (macassarensis) .. 115 nagaraja (europa) .................. 176
maenada (maeonides) ............ 232 menadensis (Parantica) ................ nais (Cyrestis) ................... 26, 27
maeonides (Cupha) ................ 232 .......................... 25, 215, 216 najara (Acytolepis) ................ 162
maevis (Taractrocera) .............. 28 menado (Faunis) .................... 169 nakamotoi (thetis) .................. 120
magnus (sabina) .................... 211 mendice (jopas) ...................... 177 namusa (theda) ...................... 130
magou (Euploea) .... 29, 223, 16/1 Menelaides ............. 86, 4/1, 4/6-7 nanae (Deramas) ................... 119
mahinta (iluska) ...................... 56 menyangka (kurava) .............. 143 narada (Amblypodia) ... 126, 7/10
major (Allotinus) ................... 115 meridionirga (melanippus) .... 222 narina (Libythea) ................... 168
makassara (limniace) ............. 219 merionoides (Ariadne) .................. navus (japetus) ........................ 63
makitai (aratus) ..................... 150 ............................. 191, 12/11 nectareus (lymire) ................. 195
malaya (Megisba) ......... 159, 8/26 mesolamprus (kuehni) ...... 83, 3/8 Nemeobiinae ....................... 165
manea (Rapala) ...................... 136 metagenes (fuscus) .................. 88 neolymira (lymire) ................. 196
mangola (Plastingia) ............... 67 metallica (sanaya) .................. 143 Neopithecops .......................... 158
mangolensis (oblongomaculatus) meyeri (Graphium) 24, 25, 93, 5/2 nephele (Appias) .................... 107
......................................... 81 meyeri (westwoodii) .............. 225 Neptina ................................. 197
mangolianus (solon) .............. 186 Miletinae ...................... 113, 118 Neptis .. 18, 197, 198, 200, 12/8-9
mangolicus (leos) ................... 117 Miletini ................................. 114 nerina (bolina) ....................... 213
mangolina (hewitsonii) ......... 226 Miletus ................... 116, 117, 7/4 neriotes (gigon) ........................ 87
mangolina (kalelonda) ........... 184 milon (anthedon) ............... 91, 92 neriphus (Lasippa) ....... 198, 12/7
mangolina (rahria) ................ 189 milos (fora) ............................. 112 nero (Appias) ................... 23, 109
mangolina (rochana) ............. 127 mimalon (Elymnias) .............. 174 nesimachus (Dichoraggia) ............
mangolina (tominia) .............. 100 mineus (Mycalesis) ....... 178, 179 ............................... 193, 13/8
mangolinus (gigon) ................. 87 minor (Coladenia) .................... 28 nestor (iluska) .......................... 56
manilana (Surendra) ............. 126 minor (fuscus) ......................... 88 nestor (memnon) ..................... 89
maniliana (canace) ............... 14/3 minthe (aratus) ...................... 150 newayana (horsfieldi) ............ 178
mantilis (paulinus) ................ 189 misippus (Hypolimnas) ......... 213 nicevillei (Chersonesia) ........... 26
mantra (Tajuria) .................... 131 mitisi (Delias) ........................ 107 nicevillei (Eurema) .................. 25
marabuntana (deucalion) ........ 95 mitra (trebellius) ..................... 63 nieuwenhuisi (libnites) .......... 195
marmorata (Logania) ............. 116 mixta (Hasora) ................. 58, 1/2 nigerrima (panda) ........ 110, 6/12
nigrescens (Deramas) ..... 119, 7/1 oresta (celebica) ...................... 198 Pareronia ........................ 102, 6/1
nigricans (Ypthima) ................ 18 orestias (aeropa) ..................... 202 Parnara ........................... 75, 2/21
nigrico (maeonides) ............... 232 Oriens ............................. 72, 2/16 parthenia (strigata) ................ 190
nigrolimbata (Taractrocera) ......... orithya (Junonia) ................... 210 Parthenina ............................ 200
........................... 28, 72, 2/15 Ornithoptera ...................... 79, 82 Parthenos ...................... 200, 13/4
nikaja (fettingi) ............... 73, 2/17 orsolina (jangala) ......... 133, 7/19 Paruparo ................................ 132
nimbus (avesta) ..................... 193 Orsotriaena .................. 176, 10/8 parvimacula (rhesus) ............... 94
nimbus (sabina) ............ 211, 14/8 orthosia (orithya) ................... 210 pasithoe (Delias) .................... 106
nina (Leptosia) ............... 103, 104 osima (daria) .......................... 200 paska (subperusia) ................. 142
Nirvana .................................. 181 otis (Zizina) .................. 156, 8/21 Pathysa ............................. 93, 5/5
Nirvanopsis .......... 21, 181, 10/14 owstoni (Burara) ..................... 56 paulina (Appias) .................... 110
nita (omaha) ............................. 72 oxynthas (choaspes) ............... 219 paulinus (Cyrestis) .... 26, 27, 189
nitebis (Charaxes) .................. 185 Pachliopta ............. 79, 83, 84, 3/2 paupercula (jopas) ................. 177
niuwenhuisi (menadensis) .... 217 pactolides (pactolus) .............. 142 pava (Potanthus) ..................... 73
nivea (Cyrestis) ................. 26, 27 pactolus (Nacaduba) .............. 142 pavana (Nacaduba) ................ 142
noctesco (libnites) .................. 195 Paduca ................................... 233 pecten (merionoides) .............. 191
nora (Prosotas) ............... 145, 8/6 palajava (asmara) ............. 61, 1/6 peisandrus (nesimachus) ....... 193
norbana (blanda) ..................... 99 palata (eleusina) .................... 226 pelengensis (androcles) ............ 94
norma (Ypthima) ................... 183 palawana (Coladenia) .............. 28 pelengensis (labotas) .............. 204
normani (Nacaduba) ............. 143 palawana (marmorata) .......... 116 pelengensis (plateni) .............. 170
Notarthrinus ......................... 163 palawanus (apidanus) .... 124, 7/8 pelensis (thyonneus) .............. 190
Nothodanis ................... 146, 8/13 palinurus (Papilio) .................. 85 Pelopidas ......................... 77, 2/23
Notocrypta ........................ 66, 2/4 pallens (haliphron) .................. 81 pelurius (nesimachus) .. 193, 13/8
notus (lyncides) ..................... 196 pallesco (labotas) .................... 203 Pemara ..................................... 67
nox (Atrophaneura) ................. 82 palos (Poritia) ........................ 119 peraka (Chersonesia) ................ 26
nubilus (lycone) ..................... 196 palu (Losaria) ................... 83, 3/6 peranthus (Papilio) .... 23, 86, 4/8
nupta (sinha) ................ 234, 12/2 paluana (blanchardii) ............ 228 perimale (Cepora) .................. 111
Nymphalidae .......... 15, 23, 167 paluana (Logania) .................. 118 periya (amanda) ..................... 202
Nymphalinae ....................... 205 paluensis (Ixias) ............. 103, 5/4 permagna (syrinx) ................. 128
Nymphalini ......................... 206 pamela (angusta) ............ 142, 8/5 perseus (Mycalesis) ............... 178
Nymphalis ............................. 208 pamphylus (eurypylus) ........... 92 personata (Spalgis) ................ 119
nynias(Ypthima) ................... 183 panda (Saletara) ........... 110, 6/12 pertinax (fuscus) ..................... 88
nysa (Delias) .......................... 105 pandaea (Lohora) ................... 180 perversus (alphenor) ................ 88
nysa (mimalon) ...................... 174 panadarus (Hypolimnas) ......... 18 Petrelaea ......................... 141, 8/3
obatratus (lycone) .................. 196 pandocus (Ypthima) .............. 184 Phaedyma .............................. 200
oblongomaculatus (Troides) .... 81 panormus (Catochrysops) ..... 153 phaenareta (Euploea) ............. 224
obscura (Logania) ........... 196, 7/3 Pantoporia ................. 197, 12/6 phaenops (Arhopala) ............. 123
obscurata (japetus) .................. 63 panvila (velutina) .................. 173 phaidon (bochus) ................... 149
obsoleta (leda) ........................ 172 papayatana (fora) ................... 112 Phalanta ....... 229, 230, 234, 12/3
octaviae (tritaea) .................... 102 Papilio ........................... 4, 18, 23, phalanta (Phalanta) ............... 235
Odina ................................ 61, 1/7 ..... 30, 85, 86, 90, 4/1, 4/3-8 phalkes (antilope) ................... 213
odinia (blanda) ......................... 99 Papilionidae ......... 15, 23, 79, 85 phasiana (aeetes) .................... 201
Odontoptilum ............. 63, 1/12 Papilioninae ........................... 79 phedima (Melanitis) .............. 172
oedipodea (Burara) .................. 54 Papilionini .............................. 84 phestus (zarinda) ................... 109
ohara (Telicota) ........................ 74 Papilionoidea ......................... 31 phidippus (Amathusia) ......... 169
ohtai (Jamides) ....................... 149 paraffinis (Anthene) .............. 139 philander (Arhopala) ............. 124
olivia (varuna) ....................... 137 Paragerydus ................... 115, 7/2 philatus (Jamides) .......... 150, 151
omaha (Potanthus) .................. 72 paralysos (Notocrypta) ..... 66, 2/4 philippensis (Una) ................. 141
omarion (alcippe) ................... 235 Parantica ........ 25, 26, 215, 15/10 philippina (Caltoris) ................ 78
onyx (alcippe) ........................ 235 Paranticopsis .............. 93, 95, 5/1 philippina (Celastrina) . 162, 8/30
opaculus (janardana) ............. 178 parce (Elymnias) ..................... 18 philippina (Discophora) .......... 18
ophthalmicus (Lohora) .......... 180 parce (moluccana) .................. 236 philo (Anthene) ...................... 139
optimus (celeno) .................... 150 Pardopsini ............................ 229 philo (Parantica) ...................... 26
philo (Parantica) ...................... 26 Princeps ................................... 90 rhapia (rhesus) ......................... 94

philomela (Ypthima) .............. 183 prinsi (kuehni) ....................... 105 rhesulus (rhesus) ..................... 93
phlegeton (blanchardii) .......... 228 procles (Graphium) ................. 24 rhesus (Graphium) .............. 9, 93
phocides (Bindahara) .... 135, 7/21 Prosotas ......................... 144, 8/6 Rhinopalpa ................... 211, 14/9
phoenix (Pithecops) ...... 155, 8/25 Protoploea .............................. 223 rhodana (rhode) ..................... 148
phrikonis (cumaea) ................ 174 Prusiana ......................... 75, 2/20 rhode (Caleta) ........................ 147
Phrissura .............................. 108 prusias (Prusiana) ................... 75 Rhopalocamptinae ................ 54
phul (Burara) ........................... 55 Pseudamathusia ....... 18, 170, 9/1 ribbei (Rapala) ....................... 136
Physcon ...................... 180, 10/16 Pseudergolini .............. 188, 192 ribbei (myrina) ....................... 237
pia (Prosotas) ......................... 145 Pseudergolis ... 19, 192, 193, 13/9 ribbei (velutina) ..................... 173
picta (biblis) .................. 237, 11/4 Pseudoborbo ............................. 77 ribbei (vitrea) ......................... 218
piepersi (Ixias) ....................... 103 pseudocentaurus (Arhopala) ........ Riodinidae ...................... 15, 165
piepersianus (alphius) ........... 188 ................................ 122, 124 Riodininae ............................ 113
piepersii (Psychonotis) . 144, 8/12 Pseudocoladenia ............... 61, 1/8 Ripponia .................................. 80
Pieridae ...................... 15, 23, 96 pseudomelaneus (Parantica) ... 25 risa (Chersonesia) .................... 26
Pierinae ................................. 101 Pseudomycalesis ......... 181, 10/15 risompae (Ypthima) ............... 184
pinsbukana (Coladenia) ........... 62 pseudosias (Jamides) .............. 151 rita (Catopyrops) ................... 146
Pirdana ..................... 28, 71, 2/14 Psolos ............................. 65, 2/2 rivalis (pomona) .................... 101
pistor (haliphron) .................... 81 Psychonotis ............ 29, 144, 8/12 robusta (brassolis) ................. 114
Pithecops ...................... 155, 8/25 ptyleus (horsfieldi) ................. 178 robustus (Euripus) ....... 205, 15/4
pitya (atrax) ........................... 173 pumila (Parantica) .................. 25 rochana (Iraota) ............ 127, 7/11
placidula (Udara) .................. 160 purahu (haliphron) .................. 81 Rohana .......................... 204, 15/1
Plastingia ......................... 67, 2/7 purreea (Cupitha) ............. 67, 2/5 rolanda (phaenareta) ............. 224
platena (Symbrenthia) ..... 29, 207 pusilla (norma) ...................... 184 rona (Udara) .......................... 160
plateni (Amathuxidia) .... 170, 9/2 puspa (Acytolepis) ................. 161 rosea (polyphontes) .................. 84
plateni (Choaspes) ............ 59, 1/4 putli (Chilades) ............. 165, 8/35 rosei (Miletus) ....................... 117
pleonasma (menado) .............. 169 pylos (hecabe) ........................... 98 rosenbergi (Delias) ........ 106, 107
plexippus (Danaus) ............... 220 pyranthe (Catopsilia) ............. 100 rosimon (Castalius) ............... 154
plinius (Leptotes) ......... 155, 8/17 Pyrginae ................................. 60 rovena (maeonides) ................ 231
plutarchus (plinius) ..... 156, 8/17 Pyroneura ................................ 67 rubellio (aeetes) ...................... 201
polibete (Doleschallia) .. 214, 14/2 pyrrha (Melanitis) ................. 173 rubicundus (amanda) ............ 202
polisma (aegis) ....................... 108 pytheas (antara) ..................... 197 ruficornis (Celaenorrhinus) .... 61
polycritos (alphenor) ............... 88 quadripunctata (Hasora) ......... 57 rumanzovia (Papilio) ......... 18, 89
Polygonia ............................... 208 quercoides (Arhopala) ............ 123 russelli (Sancterila) ............... 160
polynice (Rhinopalpa) .. 211, 14/9 Rachana ........................ 132, 7/17 russelli (samarensis) .............. 115
Polyommatinae ........... 118, 138 radiosa (gomata) ...................... 55 sabina (Yoma) .............. 211, 14/8
Polyommatini .............. 138, 140 Ragadiini .............................. 181 sabina (kausambi) ......... 167, 8/37
polyphontes (Pachliopta) .. 84, 3/2 rahria (Chersonesia) 26, 189, 13/5 sabulum (phalanta) ............... 235
polytes (Papilio) ....................... 88 rahula (ohara) .......................... 74 sakit (Hasora) .......................... 57
Polytremis ...................... 77, 2/24 rama (Zopgraphetus) ............... 67 sakita (hiraca) ................. 69, 2/10
Polyura ............. 26, 27, 187, 11/2 ranga (ternatensis) .................. 74 Salanoemia ............................... 67
pomona (Catopsilia) ..... 101, 6/14 Rapala ........................... 135, 7/22 salapia (constantia) ............... 173
Poritia .................................... 119 rarior (hicetas) ....................... 174 Salatura ........................ 220, 15/8
Poritiinae ...................... 113, 118 recondita (Cirrochroa) ........... 234 salentia (sylvia) ............ 201, 13/4
Poritiini ................................. 118 redtenbacheri (Euploea) ......... 227 Saletara ....................... 110, 6/12
poros (taxiles) ............... 230, 11/5 reducta (hewitsonii) ............... 226 saleyerana (rosenbergi) .......... 107
porphyritica (echerius) .......... 167 regulus (kuehni) .................... 132 saleyerensis (venata) ............. 120
porrothenus (fuscus) ............... 88 Remelana ...................... 133, 7/19 saleyra (echerius) ................... 167
Potanthus ....................... 72, 2/17 Remelanini ........................... 133 saleyra (ida) ........................... 199
potens (lymire) ...................... 195 remulina (itys) ........... 178, 10/10 saleyra (orithya) .................... 210
prasnaja (japetus) .................... 63 repetitius (bernardus) .. 186, 11/1 samanga (Acytolepis) ... 162, 8/29
Pratapa .......................... 131, 132 resplendens (cumaea) ............ 174 samanga (butyrosa) .......... 97, 6/6
Precis ..................................... 208 rhadamantus (Troides) ............ 82 samarensis (Allotinus) .......... 115
sambawana (Delias) ................ 18 shirozui (Delias) .................... 106 sulaensis (glaucippe) ............. 102
samina (vivarna) .... 125, 126, 7/9 sibylla (satyrina) ................... 233 sulaensis (hypolitus) ............... 80
sananaensis (croesus) .............. 82 Sidima .................................... 161 sulaensis (merionoides) ......... 191
sanaya (Nacaduba) ................ 143 sikkima (malaya) .......... 159, 8/26 sulaensis (nitebis) .................. 185
Sancterila ...................... 159, 8/27 silas (rosimon) ....................... 154 sulaensis (polibete) ................ 214
sangira (alitha) ........................ 99 silayara (blanchardii) ............ 228 sulaensis (thyonneus) ............ 190
sangira (Arhopala) ................ 123 similis (Arhopala) .................. 122 sulaensis (tritaea) .................. 103
sangira (angusta) .................. 142 similis (Coladenia) ................... 28 sulana (antara) ...................... 197
sangira (cydippe) ................... 238 similliana (satyrina) .............. 233 sulana (kuehni) ...................... 105
sangira (Elymnias) ................ 174 simulatrix (Eurema) ................ 25 sulana (sylvia) ....................... 201
sangira (eurypylus) ................. 92 sinda (hecabe) .......................... 98 sulana (zarinda) .................... 109
sangira (neriphus) ................. 198 singhapura (Delias) ............... 105 sulanorum (hombroni) .......... 108
sangira (sylvia) ...................... 201 sinha (Vagrans) ............ 234, 12/2 sulanus (menado) .................. 169
sangirica (arias) ..................... 232 Sinthusa ....................... 138, 7/25 sulawesiana (Sidima) ............ 161
sangirica (Dacalana) ............. 133 sipylus (Hypolycaena) . 134, 7/20 sulawesiensis (atymnus) ..............
sangirica (glaucippe) ............. 102 siren (Hypochrysops) .............. 18 ............................... 128, 7/13
sarasinorum (tritaea) ............. 103 sirius (Mycalesis) .................. 179 sulensis (itys) ........................ 178
sari (Eurema) ........................... 25 snelleni (Jamides) .................. 149 sulewattan (Parantica) .................
sarnada (myrina) ................... 237 snelleni (dhanada) ................... 61 ............... 26, 215, 216, 15/10
sarpedon (Graphium) .. 24, 91, 92 sohmai (deliciosa) .................. 159 sulina (celebica) ....................... 62
sarsina (biblis) ....................... 237 sohmai (Horaga) .................... 129 sulphurifera (Halpe) ................ 65
sasivarna (Matapa) .................. 28 solon (Charaxes) .................... 186 sumbanus (Neopithecops) ..... 158
sataspes (Papilio) .............. 87, 4/6 sophonisbe (juventa) .............. 218 suprema (plateni) .................. 170
satellita (aeetes) ..................... 201 soror (timnatha) .................... 111 Surendra ......................... 125, 7/9
satellitica (dejone) .................. 232 sororia (diomea) ..................... 212 surprisa (Delias) .................... 106
satellitica (echerius) ............... 167 sosiphanes (flegyas) ............... 166 susanoo (dejone) .................... 231
satellitica (juventa) ................ 217 sostrata (cleander) ................. 123 suttoni (Acerbas) ..................... 71
satyrina (Algia) ............ 233, 11/8 sota (Elodina) ................. 104, 6/8 suwartinae (Deramas) ........... 119
Satyrinae .............................. 171 spadix (affinix) ...................... 185 syllus (menado) ..................... 169
Satyrinii ................................ 182 Spalgini ................................. 118 sylvester (Euploea) ................ 223
schaeffera (Nothodanis) 146, 8/13 Spalgis ............................ 118, 7/5 sylvia (Parthenos) ........ 200, 13/4
schatzi (Jamides) .................... 152 specularia (Ariadne) .............. 191 Symbrenthia .................................
scherzeri (Euploea) ................ 227 sphaerica (ida) ........................ 199 .......... 29, 206, 14/6-7, 14/11
schlegelii (sylvester) .............. 224 Spindasis ................................ 130 symethus (Miletus) ............... 117
scitillans (philo) ..................... 139 stellata (anomala) ....... 212, 14/12 symphelus (eulimene) ............ 197
scylla (Catopsilia) .................. 100 stiris (codrus) .......................... 91 Syntarucus ............................ 155
selayarensis (amanda) ........... 202 straatmani (Arhopala) ........... 124 syrinx (Horaga) ..................... 128
selayarensis (criton) ................ 82 strabo (Catochrysops) ............ 152 tabula (Cyrestis) ...................... 26
selayarensis (heracles) ........... 189 strabobinna (Catochrysops) .......... Tachyris ................................. 109
selayarensis (redtenbacheri) .. 227 ............................... 153, 8/15 Tacola ........................... 196, 14/1
selina (Horaga) ............. 129, 7/14 strigata (Cyrestis) ........... 27, 190 tagalica (Curetis) ............ 120, 7/6
sem (trebellius) ........................ 63 subardatus (dubiosa) ............. 145 Tagiades .......................... 63, 1/11
Semanga ................................ 125 subcincolor (chamunda) .......... 61 Tajuria .......................... 131, 7/16
semifusca (celebensis) ............ 205 subconcolor (chamunda) ......... 61 talantus (nigrolimbata) .. 72, 2/15
seminiger (Jamides) ............... 149 subfestivus (ancyra) ....... 146, 8/8 talauta (alimena) ................... 213
semiramis (Cirrochroa) ......... 234 subperusia (Nacaduba) .......... 142 talauta (araxes) ...................... 123
semperi (Coladenia) ................. 28 substrigatus (epius) ............... 118 talautensis (algea) .................. 226
sena (Bibasis) ........................... 56 sula (idea) .............................. 229 talautensis (aspasia) .............. 112
senata (sena) ............................ 56 sula (ternatensis) ..................... 74 talautensis (hamata) .............. 219
seneca (paulinus) ................... 189 sula (vitta) ............................... 58 talautensis (tagalica) ............. 120
sequana (juventa) .................. 217 sulaensis (amanda) ................ 203 talautica (cleona) ................... 216
serica (diomea) ....................... 212 sulaensis (erota) ..................... 231 talissa (tominia) ..................... 100
setan (Charaxes) .................... 186 sulaensis (eupator) ................ 225 taloranus (codrus) ................... 91
talyabona (fuscus) ................... 88 thyrsis (Gangara) ............. 68, 2/9 umbrosa (Lohora) .................. 180
tambora (Cethosia) ................ 237 tiglath (seminiger) ................. 149 Una ................................. 140, 8/2
tambusisiana (Idea) ...................... tilaha (Eurema) ........................ 25 unica (moestissima) ................. 48
......... 4, 23, 24, 29, 229, 16/3 tilmara (Lohora) .................... 180 unicolor (Allotinus) ............... 116
taminatus (Hasora) ................. 57 timnatha (Cepora) ........ 111, 6/11 unicolor (mycalesis) .............. 171
Tanaecia ................................. 201 timorensis (Eurema) ................ 25 unipupillata (Lohora) ............ 180
tanagra (otis) ......................... 157 timorensis (Junonia) .............. 210 urania (Appias) ............. 109, 110
tanuki (Lohora) .......... 181, 10/15 timorensis (hylas) .................. 199 Uranobothria .......... 21, 163, 8/31
taprobanus (calathus) ....... 68, 2/8 timorica (Parantica) ................ 25 usta (Una) ...................... 141, 8/2
Taractrocera . 28, 30, 31, 71, 2/15 Tirumala ............... 215, 218, 15/7 utakata (lilaea) ....................... 206
Tarattia .................................. 194 titei (normani) ....................... 143 Vagrans ........................ 234, 12/2
tarpira (jalindra) .................. 7/17 titius (epius) ........................... 7/5 vaja (colon) .............................. 73
Tarucus .................................. 153 tituria (umbretta) .................. 158 vanbemmeleni (myrina) ........ 237
taruna (affinis) ...................... 221 tityoides (Parantica) .......... 25, 26 Vanessa ...................... 207, 14/10
tawaya (juventa) .................... 217 toalarum (avesta) ......... 193, 13/9 vanoorti (eupator) .................. 224
tawayana (neriphus) .... 198, 12/7 toekangbesiensis (perimale) ... 111 varuna (Rapala) ..................... 136
taweya (chalcedonyx) ............ 129 togiana (biblis) ....................... 237 veiovis (Chilasa) ............... 85, 4/2
taxiles (Terinos) ........... 230, 11/5 togiana (lyncides) .................. 196 velitra (europa) ...................... 176
taxilus (Potanthus) .................. 73 toliana (cumaea) .................... 174 velutina (Melanitis) .............. 173
telamon (Cyrestis) ................... 27 tola (ficulnea) ................... 60, 1/5 venata (Curetis) ..................... 120
Telicota ........................... 73, 2/18 tombugensis (Petrelaea) ........ 141 ventus (dorcus) ........................ 94
Tellervini .............................. 214 tombugensis (algea) ............... 227 verelius (araxes) .................... 124
tellus (leos) ............................. 117 tombugensis (hombroni) ....... 108 verena (Sinthusa) .................. 138
telmissus (genutia) ................ 221 tominia (Eurema) ......................... verriculata (sinthusa) ... 138, 7/25
tenggara (incerta) .................. 175 ..................... 25, 30, 100, 6/2 veteratrix (imperialis) ............. 55
tephlis (Arhopala) .................. 123 tongana (Doleschallia) .......... 214 villosa (Anthene) ................... 140
Terias ................................ 98, 6/2 tontoliensis (juventa) ... 217, 15/6 Vindula ................ 229, 231, 11/6
Terinos .......................... 230, 11/5 toxopei (Parantica) .. 25, 215, 216 violae (Lethe) ......................... 176
ternatensis (Telicota) ..... 74, 2/18 transiens (Lohora) ................. 180 Virachola ............................... 137
tessa (tessellata) ....................... 68 trebellius (Tagiades) ....... 63, 1/11 virgata (Amathusia) ....... 170, 9/1
tessellata (Plastingia) . 67, 68, 2/7 tribus (Erionota) ...................... 70 visuna (pavana) ..................... 142
tessimus (horsfieldi) .............. 178 trichopepla (Cephrenes) ........... 29 vitrea (Ideopsis) ..................... 218
testa (ternatensis) ........... 74, 2/18 tritaea (Pareronia) .......... 102, 6/1 vitta (Hasora) .......................... 58
teurnia (hedonia) ................... 209 trochylus (Freyeria) ............... 165 vivarna (Surendra) ........ 126, 7/9
textrix (monticolus) ................. 91 Trogonoptera ........................... 18 vollenhovi (eleusina) ............. 226
thaliarchus (theda) ....... 129, 7/15 Troides ........... 18, 79, 80, 3/1, 3/5 volux (paralysos) .................... 2/4
Theclinae .............................. 120 Troidini ................................... 79 vulcanus (Spindasis) ............. 130
theda (Drupadia) .......... 129, 7/15 trojana (Trogonoptera) ............ 18 wallacei (hemixanthus) ........... 60
themire (Cyrestis) .................... 26 tsukadai (damar) ...................... 65 wangiwangiensis (peranthus) . 86
theresae (Cyrestis) ............. 26, 27 tsukadai (Jamides) ................. 150 wasiensis (fuscus) .................... 88
theristra (tominia) ................. 100 tsukadai (Uranobothria) 163, 8/31 watanabei (panda) ................. 110
thestius (oblongomaculatus) ... 81 tucanus (polytes) ..................... 88 wegneri (Parantica) ................. 26
thetis (Curetis) ...................... 120 tuckeri (Burara) ....................... 54 wentholti (affinis) .................. 221
thoanthea (virgata) ......... 170, 9/1 tumpa (Gangara) ............... 28, 69 westwoodii (Euploea) ............ 225
thoria (dilecta) ....................... 160 tychius (genutia) ................... 221 windorum (Acrophtalmia) ...........
thrasetes (eupator) ................. 224 Udara ............................ 160, 8/28 ............................. 182, 10/12
thrax (Erionota) ....................... 69 Udaspes .................................... 64 wiskotti (algea) ...................... 227
thule (Graphium) .................... 95 uedai (glaucippe) ................... 102 Xanthoneura ............................ 67
thule (Cirrochroa) ........ 233, 12/1 ultramontana (juventa) ......... 217 xenia (Hypolycaena) .............. 135
Thymipa ................................. 183 ulyssides (ethion) ................... 148 Xois ........................................ 183
thyodamas (Cyrestis) ......... 26, 27 umbrata (Hypolycaena) ......... 134 yaya (paralysos) ....................... 66
thyonneus (Cyrestis) .................... umbretta (Neopithecops) ....... 158 Yoma ............................. 211, 14/8
................... 26, 27, 190, 13/7 umbrina (Hasora) .................... 56 Ypthima .................. 18, 183, 10/9
Ypthimina .............................. 182 Zemeros ..................... 166, 8/36 zitenius (Melanitis) ............... 172
Yramea ................................... 229 zenica (menado) ..................... 169 Zizeeria ......................... 156, 8/20
yumikoe (cognata) ................. 187 Zethera ................. 23, 175, 10/6 Zizina ......................... 156, 8/21
zamboanga (nero) .................. 109 Zetherina .............................. 175 Zizula ........................... 157, 8/23
zarinda (Appias) .......... 9, 23, 109 ziclea (Taractrocera) .......... 71, 72 Zographetus ............ 64, 67, 2/6
zebuda (Delias) ...................... 106 zingis (plinius) ...................... 156 zondervani (Appias) .............. 109
zelia (cyta) ............................. 149 zita (alitha) .............................. 99 zylda (Rapala) .............. 136, 7/22
Zeltus ..................................... 133 zitema (unicolor) ................... 116 zyrthis (berenice) ................... 143

Butterflies of Sulawesi

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ZV-343 003-268 | vane-wright 04-01-2007 15:47 Page 3

The butterflies of Sulawesi: annotated checklist for

R.I. Vane-Wright & R. de Jong

Keywords: butterflies; skippers; Rhopalocera; Sulawesi; Wallace Line; distributions; biogeography;

This paper presents an annotated checklist of the butterflies (Lepidoptera: Rho-

1 Project Wallace Contribution 154.

As members of the Royal Entomological Society Project Wallace expedition, we

Sulawesi and its place in the Malay Archipelago

The Sulawesi Region

Outline of present-day ecology

Outline of present-day vegetation

Outline of geological evolution

Biogeography of Sulawesi butterflies

concludes that there is almost no influence of Sulawesi on the butterflies of Borneo.

total non-end SR Sul si

total 557 318 239 133 28

Non-endemic faunal elements

Faunal analysis revisited

The areas and codes

pattern percent no. of examples

pattern percent no. of examples

Are there distributional patterns on Sulawesi itself?

N C S N+C N+S C+S N+C+S N total C total S total

Endemism, and Sulawesi as a critical island fauna

Generic level endemism

Species endemism: Sulawesi as a critical island fauna

Total genera found in Sulawesi Region 194

Although the unsophisticated procedures adopted in such analyses have now

Is the Sulawesi Region an area of endemism?

Are there distribution patterns in the endemics of Sulawesi?

Celebes forewing and gigantism: other manifestations of endemism?

sarpedon group Oriental & Australian Regions

wing markings (widening of dark margin on upperside of forewings in females;

Application of phylogenetic information to biogeographic analysis renders endemic

subgenus Hestia Sri Lanka, S India to Sundaland

pumila group Papuan Region

laxmi continental Asia

Lepidoptera Linnaeus, 1758

Rhopalocera Boisduval, 1840

Key works for South East Asian and Australasian butterflies:

Hesperiidae Latreille, 1809

Coeliadinae Evans, 1937

Range.–– Palaeotropics; a small group of about 80 species, often crepuscular in

Burara Swinhoe, [1893]

B. oedipodea Swainson, 1820 (Branded Orange Awlet)

B. tuckeri Elwes & Edwards, 1897

*B. phul Mabille, 1876

*B. imperialis Plötz, 1886

*B. aphrodite Fruhstorfer, 1905

B. gomata Moore, 1865

Bibabis Moore, 1881

B. iluska Hewitson, 1867

B. sena Moore, 1865

Hasora Moore, 1881

*H. umbrina Mabille, 1891

H. chromus Cramer, 1782

H. taminatus Hübner, 1818

H. mixta Mabille, 1876

H. badra Moore, 1858

*H. sakit Maruyama & Uehara, 1992