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
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

Received: 01 October 2020

Accepted: 02 December 2020

Published: 30 March 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 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).

Abbreviations

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.

Neogalea Hampson, 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

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

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

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

Neogalea sunia (Guenée, 1852) (Figs. 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.

N. sororcula Becker, sp. n., paratype ♀.
Figs 1.
N. sororcula Becker, sp. n., paratype ♀.

N. sunia (Gn.).
Fig. 2
N. sunia (Gn.).

N. caracaraTroubridge, ♂, Brazil
Fig. 3
N. caracaraTroubridge, ♂, Brazil

N. sororcula Becker, sp. n., holotype ♂.
Fig. 4
N. sororcula Becker, sp. n., holotype ♂.

N. sororcula, aedeagus.
Fig. 5
N. sororcula, aedeagus.

N. sunia (Gn.) ♂
Fig. 6
N. sunia (Gn.) ♂

N. sunia (Gn.), aedeagus.
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, 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.

Neogalea sororcula Becker, sp. n. (Figs. 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.

N. caracara Troubridge ♂
Fig. 8
N. caracara Troubridge ♂

N. caracara Troubridge, aedeagus
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.

N. caracara Troubridge ♀
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).

Neogalea caracara Troubridge, 2020 (Figs 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.

N. sunia (Gn.), ♂
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.

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

BIBLIOGRAPHY

BAARS, J.-R., 2003.– Geographic range, impact, and parasitism of lepidopteran species associated with the invasive weed Lantana camara in South Africa.– Biological Control,28: 293-301. DOI:10.1016/S1049- 9644(03)00070-7.

BADO, S. G., PANUNZIO M. G. & ARTALE, L., 2004.– Aspectos morfológicos, biológicos y daño de Neogalea sunia Guenée (Lepidoptera, Noctuidae) sobre Lantana camara L. (Verbenaceae).– Idesia, 22: 35-43.

BARNES, W. & McDUNNOUGH, J. H., 1913.– Illustrations of rare and typical Lepidoptera (continued).– Contributions to the Natural History of the Lepidoptera of North America, 2(1): 1-47, plates I-XXI.

BECKER, V. O. & MILLER, S. E., 2002.– Large moths of Guana Island, British Virgin Islands: a survey of efficient colonizers (Lepidoptera: Sphingidae, Notodontidae, Noctuidae, Arctiidae, Geometridae, Hyblaeidae, Cossidae).– Journal of the Lepidopterists’ Society, 56: 9-44, 191-192.

COMSTOCK, J. A. & DAMMERS, C. M., 1935.– Notes on the early stages of three butterflies and five moths from California.– Bulletin of the Southern California Academy of Sciences, 33: 136-151 (1934).

DRUCE, H., 1889.– Lepidoptera-Heterocera.– In F. D. GODMAN & O. SALVIN. Biologia Centrali-Americana, 1: 490 pp.

FRANCLEMONT, J. G. & TODD, E. L., 1983.– Noctuidae.– In R. W. HODGES et al., eds. Check List of Lepidoptera of America North of Mexico: 120-159. Classey, London.

GUENÉE, A., 1852.– Histoire naturelle des insectes. Noctuélites I, 5: 407 pp.

HAYES, A. H., 1975.– The larger moths of the Galapagos Islands (Geometroidea: Sphingoidea: Noctuoidea).– Proceedings of the California Academy of Sciences, (4) 40: 145-208.

HAMPSON, G. F., 1906.– Catalogue of Lepidoptera Phalaenae in the British Museum, 6: 532 pp. Taylor and Francis, London.

HAMPSON, G. F., 1909.– Catalogue of Lepidoptera Phalaenae in the British Museum, 8: 583 pp. Taylor and Francis, London.

HODGES, R. W., 1971.– Sphingoidea.– In R. B. DOMINICK et al. The moths of America North of Mexico, 21: 158 pp. Classey and R. B. D. Publications, London.

HOLLOWAY, J. D., 1977.– The Lepidoptera of Norfolk Island: Their biogeography and ecology: 291 pp. W. Junk, The Hague.

POOLE, R. W., 1989.– Noctuidae-. Lepidopterorum catalogus 118: 1-1314.

REINERT, J. A., GEORGE, WS. W., MACKAY, A. & CAMPOS, C., 2009.– Resistance Among Lantana Cultivars to the Lantana Stick Caterpillar, Neogalea sunia (Lepidoptera: Noctuidae).– Southwestern Entomologist, 35: 51-58. doi: 10.3958/059.035.0106.

ROBINSON, G. S., 1976.– The preparation of slides of Lepidoptera genitalia with special reference to the Microlepidoptera.– Entomologist’s gazette 27: 127-132.

TODD, E. L., 1972.– A note on the generic transfer of “Catabena. esula (Druce) and new synonymy.– Proceedings of the Entomological Society of Washington, 74: 260.

TROUBRIDGE, J. T., 2008.– A generic realignment of the Onconcnemidini sensu Hodges (1983) (Lepidoptera: Noctuidae: Oncocnemidinae), with description of a new genus and 50 new species.– Zootaxa, 1903: 1-95.

TROUBRIDGE, J. T., 2020.– A new genus and 37 new Noctuid species from peninsular Florida and the Keys (Lepidoptera: Noctuoidea).– Insecta mundi, 789: 1-56.

WALKER, F., 1865.– List of the specimens of Lepidopterous insects in the collections of the British Museum, 32: 324-706. E, Newman, London.

ZHANG, B.-C., 1994.– Index of economically important Lepidoptera: 599 pp. CAB International. Wallingford, Oxon.

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