Ann. Bot. Fennici 48: 361–367
Helsinki 30 August 2011
ISSN 0003-3847 (print) ISSN 1797-2442 (online)
© Finnish Zoological and Botanical Publishing Board 2011
Bilacunaria aksekiensis (Apiaceae), a new species from
south Anatolia, Turkey
Ahmet Duran1, Bekir Doğan2,* & Hilal Ay1
1)
2)
Selçuk University, Education Faculty, Department of Biology Education, 42090 Konya, Turkey
Selçuk University, Education Faculty, Department of Science Education, 42090 Konya, Turkey
(*corresponding author’s e-mail: bdogan@selcuk.edu.tr)
Received 1 Oct. 2009, revised version received 28 Apr. 2010, accepted 4 May 2010
Duran, A., Doğan, B. & Ay, H. 2011: Bilacunaria aksekiensis (Apiaceae), a new species from south
Anatolia, Turkey. — Ann. Bot. Fennici 48: 361–367.
A new species, Bilacunaria aksekiensis A. Duran & B. Doğan (Apiaceae), is described
and illustrated from Anatolia, Turkey. It grows in open Pinus brutia forests and on
calcareous stony slopes of the Taurus Mountains in the district of Akseki (C3 Antalya
province). Bilacunaria aksekiensis is morphologically close to B. microcarpa. The
diagnostic morphological characters of B. aksekiensis are discussed. In addition, the
pollen characteristics and mericarp surface of B. aksekiensis and B. microcarpa are
examined by SEM. The geographical distribution of the new species and the morphologically related species is mapped. Bilacunaria aksekiensis is diploid with the chromosome number of 22.
The family Apiaceae includes approximately 450
genera and 3700 species (Pimenov & Leonov
1993). The largest genera in Asia are Ferula,
Bupleurum, Pimpinella, Heracleum, Seseli,
Angelica, Bunium and Prangos. The Asian countries with the greatest Apiaceae diversity are
China, Turkey, Iran, Russia and Kazakhstan.
Among these countries, Turkey has the highest diversity in Asia and probably in the world,
with 151 species in 42 genera (Pimenov &
Leonov 2004, Duran et al. 2005, Duman &
Sağıroğlu 2005, Parolly & Nordt 2005, Pimenov
et al. 2005, Özhatay & Kültür 2006, Sağıroğlu
& Duman 2007, Kandemir & Hedge 2007,
Dirmenci 2008).
The genus Hippomarathrum was previously
revised by Chamberlain (1972) for the Flora
of Turkey. Traditionally Hippomarathrum is
divided into two genera according to carpologi-
cal differences (Pimenov & Tikhomirov 1983):
Bilacunaria and Cachrys. Bilacunaria has four
species, mainly distributed in Anatolia, Armenia,
Cyprus, Iran, Israel, Transcaucasia and Syria
(Davis 1972, Meikle 1977, Rechinger 1987,
Shishkin 1950, Zohary 1987). Two of them, B.
microcarpa and B. scabra, are distributed in
the southeast and east Anatolia. The Mediterranean species of Hippomarathrum are placed
in Cachrys (Pimenov & Tikhomirov 1983). That
genus has two species in Turkey, C. crassiloba
and C. cristata, which mainly grow in southwest
and west Anatolia.
Bilacunaria differs from Cachrys primarily
in its fruit characters. Bilacunaria species have
almost round fruits with indistinct ridges and
projections on the surface. In anatomical studies of the fruits of Bilacunaria, the cross-section
appears round with two lacunae in the funiculus.
362
There are five ridges on each mericarp and five
vascular bundles beneath the ribs. Cachrys species have oblong or ovate and relatively large
fruits with conspicuous ridges and projections
on the surface. Cachrys species do not have
lacunae in the funiculus; however, there is sclerification throughout the mesocarp layer. Therefore, it is possible to distinguish Bilacunaria
from Cachrys according to fruit characteristics
(Pimenov & Tikhomirov 1983).
Turkey has two native Bilacunaria species:
B. microcarpa and B. scabra, distributed in Anatolia. In this paper, a new species is added to the
genus.
The Bilacunaria specimen did not have fruits
when it was collected in 2005. Specimens with
fruits were collected from the same locality
in 2008. The specimens were not referable to
any known Bilacunaria or Cachrys species. The
study of the specific descriptions of Hippomarathrum given in Chamberlain (1972), Herrnstadt
and Heyn (1972, 1977), Tutin (1968), Zohary
(1987), Shishkin (1950), Rechinger (1987),
Pimenov and Tikhomirov (1983), Pimenov and
Leonov (1993), Meikle (1977) and GruenbergFertig et al. (1973) as well as the comparison
with specimens in the herbaria KNYA, ANK,
GAZI, HUB, ISTE and K showed that the specimens represented a species new to science.
Each provided numerical value is the average
of ten measurements from different specimens.
The specimens of Bilacunaria aksekiensis were
examined and compared with specimens of the
morphologically similar B. microcarpa and B.
scabra.
Pollen grains were prepared for examination by light microscopy according to Wodehouse (1935), and the measurements were made
with an Olympus BX-50 microscope. The pollen
diameter measurements are based on ca. 50
samples and the other characters on approximately ten. For SEM study, the pollen grains and
mericarp surfaces were coated with gold, and
the micrographs were obtained using an Oxford
Leo-440 microscope. The descriptive terminology of Erdtman (1969) was followed.
For the study of somatic chromosomes, root
tips were obtained from germinated seeds, which
were pre-treated in a-monobromonaphthalene
overnight and then fixed in alcohol:acetic acid
Duran et al.
•
ANN. BOT. FENNICI Vol. 48
(3:1). Roots were hydrolyzed in 1 N HCl at
60 °C for 16 minutes and stained in Feulgen; in
addition, squashes were made in 1% lactopropionic orcein. Permanent slides were made in
Depex. Chromosome measurements were based
on at least five metaphase plates.
Bilacunaria aksekiensis A. Duran & B.
Doğan, sp. nova (Figs. 1–3)
Species plantis perennibus; caulibus glabris;
foliis segmentatis 25–60 ¥ 0.4–0.7 mm, glabris, apiculatis; radiis 7–22 mm longis, asperis;
bracteis 4–5; petalis puberulis; stylis 4–6 mm
longis; fructibus 5–6 ¥ 6–6.5 mm, distincte aculeatis diversa.
Type: Turkey. Antalya: Akseki, Çukurköy, Alçaktepe,
Kocaöz vicinity, 920 m, 7.VIII.2005 A. Duran 7087 (holotype KNYA; isotypes GAZI, ANK, HUB, and Selçuk University, Herbarium of Education Faculty).
Perennial, monocarpic, 70–130 cm tall,
thickened rootstock cylindrical-oblong, vertical, 3–6 cm in diameter. Stem stout, glabrous,
sparsely or densely resinous at surface, distinctly sulcate, angular or ± terete, entirely much
branched, with a weakly developed fibrous collar
3–6 cm long, 4–8 cm diameter at base, lower
and middle stem sometimes slightly purplish.
Basal leaves broadly oblong to obovate in outline, 50–75 ¥ 40–60 cm (including petiole), petiole with weakly developed sheath, lamina 5–7
pinnate, primary segments 3 and remote, ultimate segments linear, filiform, 25–60 ¥ 0.4–0.7
mm, apiculate, glabrous. Petioles ± flattened,
12–17 cm long. Lower cauline leaves partly
reduced, semiamplexicaule, broadly obovate in
outline, middle and upper cauline leaves gradually reduced to flowering parts, especially upper
cauline leaves much reduced, sessile, sometimes
slightly asperulous, 1–2 pinnate or few segments, or lobed to entire. Inflorescence much
branched, the branches ascending to erect, alternate, opposite or in whorls 3 or more, upper
flowering branches very dense, leaves at base
of lateral branches reduced to oblong sheath.
Flowers hermaphrodite. Umbels 5–8 rayed, rays
7–22 mm long, equal, asperulous; bracts 4–5,
(3–)5–10(–15) ¥ 0.8–1.2 mm, linear-lanceo-
ANN. BOT. FENNICI Vol. 48
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Bilacunaria aksekiensis, a new species from Turkey
363
Fig. 1. Holotype of Bilacunaria aksekiensis.
late, acuminate, slightly asperulous, persistent. Umbellules 9–11-flowered, when ripe 2–9,
4–6 mm long, asperous. Bracteoles 5–8, 2–5 ¥
0.7–1 mm, linear-subulate, slightly asperulous.
Sepals nearly obsolate, ca. 0.5 mm, ± rounded,
yellow, minutely puberulent. Petals yellow, 0.7–
1.0 ¥ 0.8–1.0 mm, oblong, strongly incurved,
puberulous externally. Stylopodium flattened,
with an undulate margin, not embedded in corky
pericarp; style clearly long, slightly curved at the
upper part, graceful conical, minutely scabridu-
lous especially lower part, 4–6 mm long; stigma
capitate. Mericarps mostly well-developed,
didymous or slightly unequal. Mature fruits 5–6
¥ 6–6.5 mm, broadly oblong, aculeate. Chromosome number: 2n = 22 (in holotype). Flowering
June–July, fruiting July–August.
Bilacunaria aksekiensis appears to be
endemic to south Anatolia and thus belongs to
the East Mediterranean floristic element. The
specimens were collected in Akseki (Antalya
province), where the species appears to be rare
364
Duran et al.
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ANN. BOT. FENNICI Vol. 48
Fig. 2. — A: Habitat of
Bilacunaria aksekiensis.
— B: Habitat of B. microcarpa. — C: General view
of the type locality of B.
aksekiensis.
Fig. 3. Cross-section of mericarp of Bilacunaria aksekiensis.
and local (Fig. 4). Bilacunaria aksekiensis grows
on calcareous stony slopes in open Pinus forest
and scrubs of Conringia grandiflora, Rhamnus
nitidus, Cotinus coggygria, Rhus coriaria, Pistacia terebinthus subsp. terebinthus, Cercis siliquastrum subsp. hebecarpa, Colutea cilicica,
Astragalus lusitanicus subsp. orientalis, Ononis
viscosa subsp. breviflora, Crataegus monogyna
subsp. monogyna, Ferulago cassia, Valeriana
dioscoridis, Xeranthemum annuum, Helichrysum pamphylicum, Styrax officinalis, Fraxinus
ornus subsp. cilicica, Phlomis grandiflora var.
grandiflora, Micromeria myrtifolia, Quercus
Fig. 4. Distribution map of Bilacunaria aksekiensis (),
B. microcarpa () and B. scabra () in Turkey.
infectoria subsp. boissieri, Q. coccifera, Ostrya
carpinifolia and Piptatherum coerulescens.
Mericarp surfaces and pollen grains of B.
aksekiensis and B. microcarpa were studied by
SEM. The mericarp surface of B. aksekiensis is
aculeate whereas in B. microcarpa it is verrucose
(Fig. 5). The pollen grain characteristics of B.
aksekiensis and B. microcarpa are compared in
Table 1 and Fig. 6.
Bilacunaria aksekiensis is clearly related to
B. microcarpa, which is endemic in south Anatolia. The former differs from B. microcarpa
mainly by the characters given in Table 2.
Bilacunaria aksekiensis also resembles B.
ANN. BOT. FENNICI Vol. 48
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Bilacunaria aksekiensis, a new species from Turkey
365
Fig. 5. SEMs of fruits. — A
and B: Bilacunaria aksekiensis. A: General shape.
B: Details of surface. — C
and D: B. microcarpa. C:
General shape. D: Details
of surface.
Fig. 6. SEMs of pollen
grains. — A and B: Bilacunaria aksekiensis. A:
General shape. B: Details
of surface. — C and D:
B. microcarpa. C: General
shape. D: Details of surface.
scabra, which grows in southeast Anatolia,
Cyprus and Syria. The former differs from B.
scabra by its glabrous (vs. hairy) stems; not
swollen nodes (vs. swollen); oblong–obovate,
5–7 pinnate basal leaves (vs. broadly oblong-
obovate, 4–5 pinnate); umbels with 5–8 rays,
7–22 mm long, slightly asperous (vs. 4–5 rays,
10–20 mm long, ± unequal, scabridulous);
slightly puberulous sepals (vs. papillose–puberulous); 4–6 mm long styles (vs. 1–3 mm long) and
Duran et al.
366
Fig. 7. Somatic metaphase chromosomes of Bilacunaria aksekiensis. Scale bar 5 µm.
oblong, 5–6 ¥ 6–6.5 mm fruits (vs. globose, 4–5
¥ 4–5 mm).
Bilacunaria aksekiensis has 2n = 22, which
is the basic number in the genus Bilacunaria
(Fig. 7). Also B. boissieri, B. microcarpa and
Table 1. Pollen morphology of Bilacunaria aksekiensis
and B. microcarpa.
Pollen morphology
Polar axis (µm)
Equatorial axis (µm)
P/E
Exine thickness (µm)
Intine thickness (µm)
Shape
B. aksekiensis
B. microcarpa
29.43 ± 1.2
15.35 ± 1.1
01.91
01.43 ± 0.7
00.75 ± 0.2
subprolate
29.24 ± 1.2
13.99 ± 1.1
02.09
01.75 ± 0.7
00.81 ± 0.2
perprolate
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ANN. BOT. FENNICI Vol. 48
B. scabra have 2n = 22 (Pimenov & Vassilieva
1983).
Palaeopalynological data show that Anatolia
had a dense vegetation cover in the last interglacial period. The topography of Turkey has
changed many times since then, which resulted
in different microclimates in the tectonic valleys (Gemici 1993). The Taurus Mountains are a
botanically interesting area located in the Mediterranean phytogeographical region and very
rich in local endemic plants (Duran et al. 2005).
Bilacunaria aksekiensis grows in the Taurus
Mountains, which are affected by the Mediterranean Sea (Fig. 2C). Recently several new species
have been described from this region, including Linaria dumanii, Arabis davisii, Centaurea
antalyensis (Özhatay & Kültür 2006), Chaerophyllum aksekiense (Duran & Duman 1999),
Tordylium ketenoglui (Duman 2000), Peucedanum isauricum (Parolly & Nordt 2004), and
Astragalus antalyensis and A. cedreticola (Duran
& Podlech 1999).
AddiTionAl specimens exAmined. — Bilacunaria aksekiensis (paratypes): Turkey. C3 Antalya: Akseki, Çukurköy,
Alçaktepe, Fireklidünek vicinity, 1000 m, 2005 A. Duran
7074 (KNYA, GAZI); ibid., 2005 A. Duran 7087 (KNYA);
ibid., 2007 A. Duran and M. Öztürk 7498 (MR); Antalya:
Akseki, Çukurköy, north of Kavzan Dağı, Saytaş vicinity,
ca. 1150 m, 2008 A. Duran 8134 (MR). — Bilacunaria
microcarpa: Turkey. A5 Amasya: Direkli, S. Peker 1545
(GAZI); A7 Gümüşhane: 1968, T. Baytop s.n. (ISTE); Erzurum: Aşkale-Bayburt road, A. Duran 6012 (MR); A9 Kars:
between Karaurgan-Sarıkamış, A. Duran 6825 (MR); B5
Yozgat: Akdağmadeni, T. Ekim & A. Değerli 4098 (ANK);
B6 Kahramanmaraş: Göksun-Sarız road, A. Duran 6867
(MR); B7 Erzincan: Erzincan-Sivas road, M. Dinç 2841 and
Table 2. A comparison of the diagnostic characters and fruit anatomy of Bilacunaria aksekiensis and B. microcarpa.
Character
B. aksekiensis
B. microcarpa
Stem
Basal leaves
Terminal segments
glabrous
oblong-obovate
25–60 ¥ 0.4–0.7 mm, glabrous, apiculate
Umbels
Bracts
Petals
Style length (mm)
Fruit shape
Fruit surface ornamentation
Endosperms
5–8 rays, 7–22 mm long, slightly asperous
4–5
outer surface puberulous
4–6
broadly oblong, 5–6 ¥ 6–6.5 mm
distinctly aculeate
horseshoe-shaped
glabrous to ± slightly asperous
obconical
10–30 ¥ 0.5–2 mm, ± hispidulous,
acuminate
7–10 rays, 20–40 mm long, ± glabrous
5–8
glabrous
1.5–2
oblong-globose, 3–5 ¥ 4–6 mm
obtuse-verrucose
horseshoe-shaped, tips of endosperm
slightly curved
ANN. BOT. FENNICI Vol. 48
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Bilacunaria aksekiensis, a new species from Turkey
A. Duran (MR); B8 Bingöl: between Göymük-Kanlıova, T.
Baytop 18267 (ISTE); B9 Ağrı: Tutak-Ağrı road, A. Duran
7531 (MR); C5 Niğde: Ulukışla, A. Duran 7645 (MR). —
Bilacunaria scabra: Turkey. C7/8 Diyarbakır/Mardin: in
Mesopotamia inter Diyarbakır et Mardin, Kotschy 322 (isotype K, photo!); Şanlıurfa: Ceylanpınar, H. Ay 1001 (MR);
C8 Mardin: Dargeçit-Midyat road, A. Duran 7958 (MR).
Acknowledgements
We express our thanks to TÜBİTAK (project no. TBAG105T355) and The Scientific Investigation Projects Coordinate Office of The Selçuk University (project no. 05401046)
for financial support.
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