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Becker 2021 - The New World Ocnonemidinae Genus NOCT

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7/30/22, 3:30 PM The New World Ocnonemidinae genus Neogalea Hampson, 1906 (Lepidoptera: Noctuidae)

Artículos
The New World Ocnonemidinae genus
Neogalea Hampson, 1906 (Lepidoptera:
Noctuidae)

El género Neogalea Hampson, 1906 de


Onconemidinae del Nuevo Mundo (Lepidoptera:
Noctuidae)

V. O. Becker becker.vitor@gmail.com
Reserva Serra Bonita, Brasil

The New World Ocnonemidinae genus Neogalea Hampson, 1906 (Lepidoptera: Noctuidae)
SHILAP Revista de lepidopterología, vol. 49, núm. 193, pp. 47-54, 2021
Sociedad Hispano-Luso-Americana de Lepidopterología

Recepción: 01 Octubre 2020


Aprobación: 02 Diciembre 2020
Publicación: 30 Marzo 2021

Abstract:
The genus Neogalea Hampson, 1906 is reviewed, including three species. N. sunia (Guenée, 1852) with
Pan- American distribution, N. caracara Troubridge, 2020 known from the Florida Keys and Brazil and
a new one restricted to a specific region of Brazil: Neogalea sororcula Becker, sp. n. (Semiarid or
Caatinga biome). A key to species, diagnosis, descriptions, and illustrations for the three species are
presented.

Keywords:
Lepidoptera, Noctuidae, Neogalea, taxonomy, diagnosis, distribution, Brazil.

Resumen:
Se revisa el género Neogalea Hampson, 1906, incluyendo tres especies: N. sunia (Guenée, 1852) con
distribución Panamericana, N. caracara Troubridge, 2020 conocida de los Caicos de la Florida y de
Brasil, y una nueva N. sororcula Becker, sp. n., restringida a la región semiárida de la Caatinga en
Brasil. Se presenta una clave para las especies, diagnosis, distribuciones e ilustraciones de las tres
especies.

Palabras clave:
Lepidoptera, Noctuidae, Neogalea, taxonomía, diagnosis, distribución, Brasil.

Introduction

Neogalea Hampson, 1906, has been regarded as a monotypic genus since it was proposed
to accommodate N. braziliensis Hampson, 1906. TODD (1972: 260) synonymized N.
braziliensis under N. esula (Druce, 1889), and HAYES (1975: 173), described N. esula
longfieldae Hayes, 1975, a form from the Galapagos Archipelago. POOLE (1989: 681), treated
all these names, in the Cuculliinae, as synonyms of N. sunia (Guenée, 1852). A second species:
N. caracara Troubridge, 2020 was just described, based on a single male from the Florida Keys
and is here recorded for Brazil for first time. Neogalea sunia is a common species throughout
the neotropical region, whose caterpillars feed on Lantana species, and for this reason has
been introduced into several countries as a biological control agent (ZHANG, 1994: 333). The
genus was listed in the Oncocnemidini by FRANCLEMONT & TODD (1983: 146), next to

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7/30/22, 3:30 PM The New World Ocnonemidinae genus Neogalea Hampson, 1906 (Lepidoptera: Noctuidae)
Catabena Walker, 1865, and by TROUBRIDGE (2008: 59) (as Oncocnemidinae) between
Catabenoides Poole, 2002 and Calophasia Stephens, 1829.

Materials and methods

This review is based on 88 specimens (including nine genitalia slides), 32 in VOB, 56 HTC,
and on the type-material in NHMUK. Synoptic collections representing the Noctuidae species
in VOB were taken to the last institution and to USNM and compared with their collections in
previous years. The global coronavirus quarantines prevented travel or borrowing specimens
during the preparation of this manuscript, but it was possible to examine images of the USNM
specimens, including seven genitalia slides. The holotype of the new species is provisionally
deposited in VOB, and will be transferred, together with the collection, to a Brazilian
institution in the future. Genitalia were prepared following the methods described by
ROBINSON (1976). Terms for morphological characters follow HODGES (1971).

A bbreviations

CNC Canadian National Collection, Ottawa, Canada

FW Forewing

G. s. genitalia slide

HTC Hubert Thöny Collection, Camacan, Bahia, Brazil

HW Hind wing

NHMUK Natural History Museum, United Kingdom

MNHN Muséum Nationale d’Histoire Naturelle, Paris, France

USNM National Museum of Natural History, Smithsonian Institution, Washington, USA

VOB Vitor O. Becker collection, Serra Bonita Reserve, Camacan, Bahia, Brazil

Results

The large series of specimens studied revealed that three species belong to Neogalea, one
of them new. All species are described, and diagnosis, and illustrations of both adults and
genitalia are presented allowing the identification of the species.

N eogalea H ampson , 1905

TS: Neogalea braziliensis Hampson, 1905. Cat. Lep. Phal., 6: 8

Diagnosis: Medium size; FW 12-16 mm (28-36 mm wingspan), gray to dark gray, ante- and
postmedial bands indistinct, ill-defined; HW translucent white, margins narrowly fringed gray.
Abdomen with a pad with long bristles at 2nd sternite. Male genitalia symmetrical; uncus long,
evenly curved, apex sharp; sacculus broad, 2/3 as long as valva, sacculus process long,
tapering distad, strongly bent towards costa. Aedeagus as long as valva; vesica with a small
sac with pouch of small cornuti near base, rows of long, thin spines distad. Female genitalia
with ostium wide, ductus bursae short, with sclerotized area before corpus bursae; corpus
bursae globose or elongate, signum present or absent; appendix bursae large; both corpus
and appendix bursae wrinkled.

Distribution: New World Tropics, from southern United States, to southern Brazil and
Argentina.

Remarks: TODD (1972: 260) regarded Neogalea Hampson, 1906 as distinct to Catabena
Walker, 1865 on the base of the corona, formed by a multiple row of long, thin bristles,
whereas in Catabena (where he included all the species currently in Catabenoides Poole,
2002), it is formed by a single row of stronger bristles along the apical margin.

There is a lineage of species that are externally similar to Neogalea in Central America and
the Caribbean which are near Neogalea and Catabenoides but differ from both in male
genitalia. The sacculus processes are long, straight, pointing to the apex of valva, whereas in
Neogalea they are angled towards costa (examples include USNM ENT 01276341, 01343384,
01343385, and VOB 14210, 72842, 121899, 129151). Thus, any critical identifications of
Neogalea from south of the United States should include examination of male genitalia.

Key to species: male genitalia

1. Valva strongly constricted ...........caracara

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Valva with margins parallel .........................2

2. Sacculus process single ..................sunia

Sacculus process branched ..........sororcula

N eogalea sunia (G uenée , 1852) (F igs . 2, 6, 7, 11)

Xylomyges sunia Guenée, 1852. Hist. nat. Ins., Noct., 1: 149

Holotype ♂, [US Virgin Islands ]: St. Thomas, [no further data] (MNHN) [image examined].

= Neogalea braziliensis Hampson, 1905. Cat. Lep. Phal., 6: 8

Holotype ♀, BRAZIL, Rio de Janeiro, Rio de Janeiro (NHMUK) [examined]

= Xylina esula Druce, 1889. Biol. Cent. Amer. Lep.-Het., 1: 297, pl. 28, fig1

Holotype ♂, MEXICO, Tabasco, Teapa (NHMUK) [examined].

= Neogalea esula longfieldae Hayes, 1975. Proc. Calif. Acad. Sci., 40(7): 173

Holotype ♂, Ecuador , Galápagos Archipelago, Isabela Island, Tagus Cove, 150 ft, 3-VIII-1924
(Collenette) (NHMUK) [examined].

Diagnosis: Sexes similar (Fig. 2). FW 13-15 mm (30-35 mm wingspan), gray; veins marked
dark gray; mixed with white scales; antemedial band indistinct, postmedial ill-defined, serrate,
slightly visible from M3 to dorsum. HW translucent white, thin, gray margin, broadening
towards apex, veins gray towards margins. Abdomen gray, whitish ventrally. Male genitalia
(Fig. 6): Sacculus process long, tapering distad, bent in a straight angle towards mid costa;
aedeagus (Fig. 7) as long as valva, vesica with row of long, thin spines. Female genitalia
(Fig.11): Ostium bursae wide; ductus bursae with short membranous base, sclerotized distad;
corpus bursae globose, signa indistinct; appendix bursae half the size of corpus bursae; both
corpus and appendix bursae finely wrinkled.

Figs 1.

N. sororcula Becker, sp. n., paratype ♀.

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Fig. 2

N. sunia (Gn.).

Fig. 3

N. caracaraTroubridge, ♂, Brazil

Fig. 4

N. sororcula Becker, sp. n., holotype ♂.

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Fig. 5

N. sororcula, aedeagus.

Fig. 6

N. sunia (Gn.) ♂

Fig. 7

N. sunia (Gn.), aedeagus.

Material studied: 61 ♂♂ (5 g. s.), 24 ♀♀ (1 g. s.). Mexico , Chiapas, Villas las Rosas, 1300 m, 1
♂, 27-VI-1981 (Becker 43347) (VOB); San Luis Potosi, Cerro Potosi, 2800 m, 1 ♂ (g. s. 5563), 26-
VI- 1997 (Becker 110281) (VOB); Ciudad Maiz, 1200 m, 1 ♂ , 24-VI-1997 (Becker 110135);
Tamaulipas, San Fernando, 50 m, 1 ♂, 1 ♀, 28-VI-1997 (Becker 110454) (VOB); Gómez Farias,
1200 m, 1 ♂, 2 ♀♀, 29-31-VII-1988, 26-V-1997 (Becker 69241, 108952) (VOB); Cuba : Santiago,
Gran Piedra, 1200 m, 1 ♂, 1 ♀, 20-VII-1980 (Becker 72841) (VOB); British Virgin Islands , Guana
Island, 80 m, 4 ♂♂ (g. s. 5595), 9-23-VII-1987, X-1989 (Becker & Miller 66610, 70709); US Virgin
Islands , St. Thomas, 300 m, 1 ♂ (g. s. 5562), 25-30-VII-1987 (Becker 66997) (VOB); Ecuador :
Loja, Catamayo, 1300 m, 1 ♀ (g. s. 5564), 20-XII-1992 (Becker 102614) (VOB); Brazil : Bahia,

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Camacan, 15º23’S - 39º33’W, 800 m, 6 ♂♂ (g. s. 5565), 21-30-IX-1991, 9-20-IV-2005, VI, VIII-2010,
II-2012 (Becker 83593, 136287, 145870, 146654, 148636) (VOB); Porto Seguro, 16º27’S -
39º03’W, 40 m, 1 ♀ (g. s. 5566), 6-8-X-2008 (Becker 140962) (VOB); Ceará, Pacatuba, 250 m, 1
♀, 6-IV-19914 (Becker 91566) (VOB); Espirito Santo, Santa Leopoldina, 650 m, 25 ♂♂, 11 ♀♀,
10-25-XI, 8-20-XII-1996, 10-25-I, 15-IV, 10-VI-10- VII, 20-VIII, 15-X-1997, 2-29-IV-1998, 1-19-V; 1-
31-XI-1999, 1-3-III-2000 (Thöny) (HTC); Minas Gerais, Sete Lagoas, 720 m, 20-V-1974 (Becker
2886) (VOB); Poté, 500 m, 2 ♂♂, 1 ♀, 15-XI-1985, 30-IV-1996,15-II-1997 (Thöny) (HTC); Paraná,
Curitiba, 920 m, 1 ♂, 25-X-1975 (Becker 3394) (VOB); Tijucas do Sul, Castelhanos, 500 m, 7 ♂♂,
7 ♀ ♀ , 2-29-V-1999 (Thöny) (HTC); Rio de Janeiro, Arraial do Cabo, 50 m, 3 ♂ ♂ , 29-I-1985
(Becker 55406) (VOB); Santa Catarina, São Bento do Sul, 800 m, 2 ♂ ♂ , 2-9-VII-1998 (Thöny)
(HTC); USA Hawaii , Oahu, Honolulu, 1 ♂, 16-28-II-1992 (Becker & Miller) (VOB).

Distribution: Widely distributed throughout the New World tropics, from southern USA,
south to Argentina and southern Brazil. Specimens in USNM indicate it is widespread in
Southern California, Arizona, and Texas, and occasionally collected in Florida. It has been
intentionally introduced into Australia, Hawaii, New Caledonia, and South Africa as a biological
control of weedy Lantana species (ZHANG, 1994: 333). The South African introduction was
apparently not successful (BAARS, 2003).

Remarks: A common species, occurring in all kinds of biomes, from sea level up to 2800 m,
especially in open, disturbed areas, where Lantana species grow as invasive, pioneer plants.
COMSTOCK & DAMMERS (1935) and REINERT et al. (2009) described the biology of sunia in
California and Texas, respectively. BADO et al. (2004) described the morphology of all
development stages (including six instars), biological traits and damage in Argentina. Male
genitalia (Fig. 5) of specimens from St. Thomas, the type locality of sunia, from Mexico,
Ecuador and from Brazil are consistently similar. Similar to sororcula and caracara, easily
distinguished from those by the shape of genitalia: sacculus process a single, long, curved rod
in sunia whereas forked in sororcula; valva strongly constricted, with large sacculus in
caracara.

Hampson treated this species in three different places, once in the Cuculliinae, as Neogalea
braziliensis Hampson, 1906: 7, and twice in the Acronyctinae: esula Druce in Catabena Walker
(HAMPSON, 1909: 234), and sunia Guenée, in Xylomyges Guenée, 1852 [= Spodoptera
Guenée, 1852] as the senior synonym of albula (Walker, 1857) (HAMPSON, 1909: 274). TODD
(1972: 260) synonymized braziliensis under esula and treated both as Neogalea. POOLE (1989:
681) established the synonymy as treated above.

The wings have been figured multiple times including BARNES & MCDUNNOUGH (1913: pl.
9), HAYES (1975), HOLLOWAY (1977), BECKER & MILLER (2002) and BADO et al. (2004) but the
genitalia have evidently never been figured.

N eogalea sororcula B ecker , sp . n . (F igs . 1, 4, 5, 12)

Material examined: Holotype 1 ♂ , BRAZIL, Bahia, 9 km W of Boa Nova, 14º36’S - 40º26’W,


750 m, 4-XII-2013, g. s. 5567 (Becker 150604) (VOB). Paratypes: 1 ♀, g. s. 5568, same data as
holotype (VOB); 1 ♂, Idem, Jussiape, 700 m, 1-30-XI-1997 (Thöny) (HTC).

Diagnosis: Sexes similar. FW dark gray; darker between ante- and postmedial bands; HW
translucent white, slightly dusted gray around apex. Male genitalia symmetrical, sacculus
process forked distad, as sharp pointed, asymmetrical Y. Female genitalia: Female genitalia
with sclerotized area before corpus bursae larger than in sunia; corpus bursae oblong.

Description: Sexes similar. Male 12 mm (28 mm wingspan); female (Fig. 1) 14 mm (33 mm


wingspan). Dark gray. Labial palpi with whitish scales below; frons black, vertex whitish, thin
black line across; antenna black, some white scales on basal third. Thorax dark gray dorsally,
white ventrally. Legs gray, hind tarsi black. Patagia with thin, black line below; tegula dark
gray. FW with veins and lines between veins, black; area basad to postmedial band darker;
ante- and postmedial bands indistinct, postmedial, above dorsum edged whitish outside; two
small, elongate, white dots in the middle: one at middle of cell, the other just outside; area on
tornus, distad of postmedial band, whitish. HW translucent white, termen edged with thin,
gray line, widening towards apex. Abdomen dorsally light gray, banded with thin, white lines
whitish underside.

Male genitalia (Fig. 4): Uncus thin, long, curved rod, basal 2/3 with same diameter
throughout, tapering distad to a sharp tip; sacculus process forked, longer branch crossing
valva reaching mid costa; juxta subsquare, wider towards base. Aedeagus (Fig. 5) slightly
shorter than valva, bent ventrad; vesica with a lateral, long sac with thin, long spine at tip; two
pockets of strong cornuti at base; multiple long bristles to apex.

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Fig. 8

N. caracara Troubridge ♂

Fig. 9

N. caracara Troubridge, aedeagus

Female genitalia (Fig. 12): Ostium bursae, conical; ductus bursae short, membranous at
base, strong, widely sclerotized at distal third towards corpus bursae; corpus bursae large,
elongate; signum absent; appendix bursae smaller than corpus bursae.

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Fig. 10

N. caracara Troubridge ♀

Distribution: Brazil, Bahia, in the Caatinga biome or semiarid region Etymology: From the
Latin soror =sister; diminutive [the little sister]; feminine.

Remarks: Similar to C. sunia; slightly smaller, darker. Easily distinguished by male genitalia,
with sacculus process branched into an asymmetrical, Y-shape structure (a single process in
sunia).

N eogalea caracara T roubridge , 2020 (F igs 3, 8, 9, 10)

Neogalea caracara Troubridge, 2020. Insecta mundi, 789: 32

Holotype ♂ , USA, Florida, Munroe Co., Florida Keys, Dagny Johnson State Park, 11-III-2012
(CNC) [not examined].

Material studied three specimens (two g. s.). BRAZIL: Rondonia, Cacaulândia, Rancho
Grande, 350 m, 2 ♂♂, 1 ♀, 1-20-XI-1999, g. s. 5569, 5570 (Thöny) (VOB, HTC).

Diagnosis: Sexes similar. Male FW 17 mm (38 mm wingspan); female FW 18 mm (wingspan).


Gray; veins marked dark gray; mixed with white scales; antemedial band indistinct,
postmedial ill- defined, serrate, slightly visible from M3 to dorsum. HW translucent white,
narrowly bordered gray, broadening towards apex, veins dark towards margins. Abdomen
gray, whitish ventrally. Male genitalia: valva strongly constricted at distal third; aedeagus
slightly shorter than valva. Female genitalia: Ostium bursae wide, nearly square; corpus
bursae elongate; signa present.

Description male (Fig. 3): 17 mm (38 mm wingspan); female 18 mm (40 mm wingspan).


Gray. Labial palpi whitish below; frons black, white line above, below antenna; vertex gray;
antenna fuscous, mixed with white scales at basal half. Thorax dorsally mixed with white,
black, and fuscous scales; patagia with four horizontal, thin lines, the outside ones black. FW
veins and lines between veins dashed dark gray; mixed with white scales; antemedial band
indistinct, postmedial ill-defined, serrate, slightly visible from M3 to dorsum, white outside;
diffuse fuscous patch on tornus; termen edged with thin lunules between veins; cilia gray,
interrupted white on veins. HW translucent white, narrowly bordered gray at apex, veins dark
towards margins. Abdomen gray, whitish ventrally.

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Fig. 11

N. sunia (Gn.), ♂

Male genitalia (Fig. 8): Uncus long, curved, basal third flattened dorso-ventrally, distal two
thirds a curved rod, densely covered with long bristles, apex blunt; valva strongly constricted
at distal third; sacculus large, ventral margin evenly round, distal end tapering to a curved,
sharp pointed hook; cucullus oblong, ventral margin with a thin, long, curved, sharp pointed
process; corona a multiple row of thin, long spines; ampulla triangular; juxta trapezoidal,
wider basal; saccus converging to a sharp process in the middle. Aedeagus (Fig. 9) twice as
long as thick, straight; vesica with a group of cornuti near base, multiple, long spines distad.

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Fig. 12

N. sororcula Becker, sp. n., paratype ♀

Female genitalia (Fig. 10): Ostium wide, square, slightly sclerotized; pair of lateral, rounded
knobs at junction with ductus bursae; ductus bursae narrow, wrinkled; corpus twice as long
as wide; wrinkled; signa a pair of opposite, long, narrow, minutely spined, with ridge along
middle; appendix bursae globose, a sclerotized band towards connection with corpus bursae.

Distribution: Southern USA (Florida Keys) and Brazil (Amazon region).

Remarks: Externally almost identical to sunia, slightly larger and paler. Genitalia much
different, especially the constricted valva with large sacculus, as shown by the illustrations.
The species was described from a single male specimen. The records from Brazil expands it is
distribution widely and brings information about its female. This manuscript was ready and
under review for publication, including the description of this species as new, when the
author received Troubridge’s publication.

Acknowledgments

Robiara U. S. Becker and Paulo Nunes (Serra Bonita Reserve) prepared the illustrations.
Hubert Thöny, Camacan, Bahia, made available the specimens in his collection. Scott E. Miller
revised the manuscript, making several corrections and suggestions that improved it greatly,
and for providing images of specimens from USNM.

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