Biodiversity Data Journal :
Taxonomic Paper
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Corresponding author: AJ Fleming (ajfleming604@gmail.com)
Academic editor: Daniel Whitmore
Received: 22 Jun 2016 | Accepted: 02 Mar 2017 | Published: 07 Mar 2017
© 2017 AJ Fleming, D. Monty Wood, M. Alex Smith, Winnie Hallwachs, Daniel Janzen, Tanya Dapkey
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Fleming A, Wood D, Smith M, Hallwachs W, Janzen D, Dapkey T (2017) Nine new species of Uramya Robineau-Desvoidy (Diptera: Tachinidae) from Area de Conservación Guanacaste in northwestern Costa Rica, with a key to their identification. Biodiversity Data Journal 5: e9649. https://doi.org/10.3897/BDJ.5.e9649
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We describe nine new species in the genus Uramya Robineau-Desvoidy, 1830 from Area de Conservación Guanacaste (ACG) in northwestern Costa Rica. All species were reared from an ongoing inventory of wild-caught caterpillars spanning a variety of families (Lepidoptera: Erebidae; Limacodidae; Megalopygidae; Lasiocampidae and Dalceridae). Our study provides a concise description of each new species using morphology, life history, molecular data, and photographic documentation. In addition to the new species the authors provide a redescription the previously described Uramya sibinivora Guimarães, which was also collected within ACG during this study. We also provide a redescription of the genus, and a revised key to species of Uramya occurring in Central and South America.
The following nine new species of Uramya, all authored by Fleming & Wood, are described: Uramya albosetulosa Fleming & Wood sp. nov., Uramya constricta Fleming & Wood sp. nov., Uramya contraria Fleming & Wood sp. nov., Uramya infracta Fleming & Wood sp. nov., Uramya lativittata Fleming & Wood sp. nov., Uramya lunula Fleming & Wood sp. nov., Uramya nitida Fleming & Wood sp. nov., Uramya pannosa Fleming & Wood sp. nov., and Uramya penicillata Fleming & Wood sp. nov.
The following are proposed by Wood as new synonyms of Uramya: Olinda Townsend, syn. nov. and Procleonice Townsend, syn. nov. The following new combination is proposed as a result of the new synonymies: Uramya brasiliensis Macquart, comb. nov. Procleonice prolixa Townsend is synonymized under Uramya brevicauda Curran, syn. nov.
tropical rain forest, tropical dry forest, cloud forest, parasitoid flies, host-specificity, caterpillars, ACG, Dexiinae, Uramyiini
Tachinidae are the second most diverse family of Diptera (
The last major taxonomic work on the Uramyini was by
All flies and rearing information described here derive from the ongoing inventory of the tri-trophic relationships between caterpillars, their food plants and their parasitoids within the dry, rain, and cloud forests of the terrestrial portion of ACG (
Our descriptions of these nine new species of Uramya build on existing knowledge and are based on differences in external morphology, COI (coxI or cytochrome c oxidase I) gene sequences, and male terminalia (when necessary). As the inventory is continually growing, it should be noted that this paper should not be taken as an indication of the final total number of species of Uramya present in ACG or Costa Rica. Our descriptions are limited only to the species known and reared from ACG. This paper on Uramya is part of a larger effort to describe new species reared during the ACG inventory (
All reared specimens were obtained from host caterpillars collected in ACG (
Species accounts presented in this paper are deliberately brief and only include basic descriptions of body morphology and coloration commonly used in the identification of Tachinidae. The descriptions are complemented with a series of color photos of every species, used to illustrate the morphological differences among them. The morphological terminology used follows
Male terminalia of Uramya spp.; a: lateral view of terminalia of U. nitida sp. nov.; b: dorsal view of terminalia of U. sibinivora Guimarães.
All caterpillars reared from the ACG efforts receive a unique voucher code in the format yy–SRNP–xxxxx. Any parasitoid emerging from a caterpillar receives the same voucher code as a record of the rearing event. If and when the parasitoid is later dealt with individually it receives a second voucher code unique to it, in the format DHJPARxxxxxxx. These voucher codes assigned to both host and parasitoids may be used to obtain the individual rearing record at http://janzen.bio.upenn.edu/caterpillars/database.lasso.
To date, all DHJPARxxxxxx-coded tachinids have had one leg removed for DNA barcoding at the Biodiversity Institute of Ontario (BIO) in Guelph, ON, Canada. All successful barcodes and collateral data are first deposited in the Barcode of Life Data System (BOLD, www.boldsystems.org) (
Inventoried Tachinidae were collected under Costa Rican government research permits issued to DHJ, and exported from Costa Rica to Philadelphia, en route to their final depository in the Canadian National Insect collection in Ottawa, Canada (CNC). Tachinid identifications for the inventory were done by DHJ in coordination with a) visual inspection by AJF and DMW, b) DNA barcode sequence examination by MAS and DHJ, and c) correlation with host caterpillar identifications by DHJ and WH through the inventory itself. Dates of collection cited for each ACG specimen are the dates of eclosion of the fly, not the date of capture of the caterpillar, since the fly eclosion date is much more representative of the time when that fly species is on the wing than is the time of capture of the host caterpillar. The collector listed on the label is the parataxonomist who found the caterpillar, rather than the person who retrieved the newly eclosed fly from its rearing container. The holotypes of the species newly described herein are all deposited at CNC.
AMNH American Museum of Natural History, New York, New York, USA
BMNH The Natural History Museum, London, United Kingdom
CNC Canadian National Collection of Insects, Arachnids and Nematodes, Ottawa, Canada
MNCR Museo Nacional de Costa Rica (formerly Instituto Nacional de Biodiversidad - INBio), Santo Domingo de Heredia, Costa Rica
MNHN Muséum National d'Histoire Naturelle, Paris, France
MZSP Museu de Zoologia da Universidade de São Paulo, São Paulo, Brazil
MRSN Museo Regionale di Scienze Naturali di Torino (collection formerly housed at Museo di Zoologia, Istituto di Zoologia e Anatomia Comparata, Università di Torino - MZUT), Turin, Italy
NMW Naturhistorisches Museum Wien, Vienna, Austria
USNM United States National Museum of Natural History, Washington, D.C., USA
Names of undescribed host species follow a standardized, interim naming system used for taxonomic units considered as distinct species and identified by DNA barcodes. The interim names are given in the format "Eois Janzen52" or "Caviria reginaDHJ01", where the "species epithet" is either composed of the name of the taxonomist who identified the species and a number or the name of a species-group followed by a code. This prevents confusion with already described species while maintaining traceability of each undescribed species within the ACG project.
DNA barcodes (DNA sequences from a standardized 5’ region of the mitochondrial cytochrome c oxidase I (COI) gene) for all ACG inventoried specimens were obtained using DNA extracts prepared from single legs using a modified glass fibre protocol (
Uramya Robineau-Desvoidy, 1830: 215. Type species: Uramya producta Robineau-Desvoidy, 1830, by monotypy.
Olinda Robineau-Desvoidy, 1830: 116. Type species: Olinda brasiliensis Robineau-Desvoidy, 1830, by monotypy. Syn. nov.
Aporia Macquart, 1846: 297 (1846: 169) (preocc. by Hübner, 1819). Type species: Aporia quadrimaculata Macquart, 1846, by monotypy.
Oxydexia Bigot, 1885: xxxiii. Type species: Oxydexia acuminata Bigot, 1885, by monotypy.
Neaporia Townsend, 1908: 67 (nom. nov. for Aporia Macquart but preocc. by Gorham, 1897). Type species: Aporia quadrimaculata Macquart, 1846, automatic [by designation of the same species (by monotypy) for Aporia Macquart, 1846].
Paraporia Townsend, 1912: 48 (nom. nov. for Neaporia Townsend). Type species: Aporia quadrimaculata Macquart, 1846, automatic [by designation of the same species (automatic) for Neaporia Townsend, 1908].
Pseudeuantha Townsend, 1915: 416. Type species: Pseudeuantha linellii Townsend, 1915 [= Lydella indita Walker, 1860], by original designation.
Uromacquartia Townsend, 1916b: 626. Type species: Uromacquartia halisidotae Townsend, 1916, by original designation.
Gymnaporia Townsend, 1919: 170. Type species: Gymnostylia fasciata Macquart, 1848, by original designation.
Orthaporia Townsend, 1919: 167. Type species: Orthaporia similis Townsend, 1919 [= Dexia longa Walker, 1852], by original designation.
Uraporia Townsend, 1919: 170. Type species: Aporia caudata Schiner, 1868, by original designation.
Anaporia Townsend, 1919: 560. Type species: Aporia limacodis Townsend, 1892, by original designation.
Procleonice Townsend, 1935: 223. Type species: Procleonice prolixa Townsend, 1935, by original designation. Syn. nov.
Thelairomima Townsend, 1935: 222. Type species: Thelairomima pictipennis Townsend, 1935, by original designation.
Other Neotropical species included in Uramya Robineau-Desvoidy
acuminata Wulp, 1890: 130 (Macquartia). Syntypes: 2 males, 3 females (BMNH) [examined by DMW]. Type localities: Mexico, Guerrero, Amula, 7,000 feet (2 males and 1 female); Omilteme (2 females).
aldrichi Reinhard, 1935: 163 (Uramya). Holotype male (USNM) [examined by DMW]. Type locality: Mexico, Oaxaca, Etla. (We have opted to leave this species out of the key on account of the holotype being too damaged; however, it most resembles U. nitens Schiner.)
brasiliensis Robineau-Desvoidy, 1830: 116 (Olinda). Holotype female (MNHN). Type locality: Brazil, Garatuba [examined by AJF]. Comb. nov. (The holotype of this species was presumed lost; after ascertaining its existence, we confirm that it belongs to the genus Uramya; unfortunately, it is too damaged to identify properly and as such we have opted to leave this species out of the key.)
brevicauda Curran, 1934: 503 (Uramya). Holotype male (AMNH) [examined by DMW]. Type locality: Venezuela, Guanoco.
prolixa Townsend, 1935: 223 (Procleonice). Holotype female (BMNH) [examined by DMW]. Type locality: Trinidad. Syn. nov.
trinitatis Thompson, 1963: 352 (Uromacquartia). Syntypes male and female (USNM) [examined by DMW]. Type locality: Trinidad, Santa Cruz Valley, Mt. Lambert.
caudata Schiner, 1868: 320 (Aporia). Syntypes: 2 males, presumed in NMW, but possibly lost. (NMW) Type locality: South America.
fasciata Macquart, 1848: 212 (Gymnostylia). Syntypes: 2 males. (BMNH) [examined by DMW]. Type locality: Brazil.
indita Walker, 1861: 306 (Lydella). Holotype male [published as female] (BMNH) [examined by DMW]. Type locality: Mexico.
elegans Giglios-Tos, 1863: 3 (Aporia). Holotype male (MRSN) [examined by DMW]. Type locality: Mexico, Tuxpango.
linellii Townsend, 1915: 416 (Pseudeuantha). Holotype female (USNM) [examined by DMW]. Type locality: Mexico, Tehuantepec.
insolita Guimarães, 1980: 198 (Uramya). Holotype male (MZSP) [examined by DMW]. Type locality: Brazil, Santa Catarina, Nova Teutònia.
longa Walker, 1853: 311 (Dexia). Holotype male (BMNH) [examined by DMW]. Type locality: South America.
similis Townsend, 1919: 167 (Orthaporia). Holotype male (AMNH) [examined by DMW]. Type locality: Brazil, Rio de Janeiro.
nubilis Townsend, 1929: 367 (Pseudeuantha). Holotype female (USNM) [examined by DMW]. Type locality: Brazil, São Paulo, Tremembé de Cantareira.
nitens Schiner, 1868: 320 (Aporia). Lectotype male (NMW), designated by Guimarães (1971) [examined by DMW]. Type locality: Venezuela.
octomaculata Townsend, 1919: 560 (Pseudeuantha). Holotype male (USNM) [examined by DMW]. Type locality: Peru, Huadquina, 5,000 ft.
penai Guimarães, 1980: 200 (Uramya). Holotype male (MZSP) [examined by DMW]. Type locality: Bolivia, Cochabamba, Chupare Locotal.
plaumanni Guimarães, 1980: 199 (Uramya). Holotype male (MZSP) [examined by DMW]. Type locality: Brazil, Santa Catarina, Nova Teutònia.
producta Robineau-Desvoidy, 1830: 216 (Uramya). Neotype male (MZSP), designated by Guimarães (1980) [examined by DMW]. Type locality: Brazil, Rio de Janeiro, Novo Friburgo, Mury.
acuminata Bigot, 1885: xxxiii (Oxydexia). Holotype male (BMNH) [examined by DMW]. Type locality: Brazil.
pictipennis Townsend, 1935: 222 (Thelairomima). Holotype female (MZSP) [examined by DMW]. Type locality: Brazil, São Paulo, São Vicente.
quadrimaculata Macquart, 1846: 297 (1846: 169) (Aporia). Holotype male (MNHN) [examined by DMW]. Type locality: Colombia.
hariola Reinhard, 1961: 206 (Uramya). Holotype male (CNC) [examined by DMW]. Type locality: Colombia.
sermyla Walker, 1849: 850 (Dexia). Holotype male (BMNH). Type locality: Brazil. (
setiventris Wulp, 1890: 129 (Macquartia). Syntypes: 2 males (BMNH and MRSN) [examined by DMW]. Type localities: Mexico: Orizaba (coll. Bellardi in MRSN); Guerrero, Omilteme, 8,000 ft (BMNH).
sibinivora Guimarães, 1980: 201 (Uramya). Holotype male (MZSP) [examined by DMW]. Type locality: Paraguay, Villarica.
townsendi Guimarães, 1980: 200 (Uramya). Holotype male (MZSP) [examined by DMW]. Type locality: Brazil, São Paulo, Mogi Guaçu, Fazenda Campininha.
umbratilis Reinhard, 1935: 164 (Pseudeuantha). Holotype female (USNM) [examined by DMW]. Type locality: USA, Texas, Donna.
venusta Wulp, 1890: 130 (Macquartia). Syntypes: 6 males (BMNH) [examined by DMW]. Type localities: Mexico, Guerrero, Amula, 6,000 ft. (1 male); Xucumanatlan, 7,000 ft. (5 males).
Head: frontal bristles not extending beyond level of pedicel; eyes haired; facial margin not visible in profile; vibrissa arising at level of facial margin; first flagellomere almost reaching facial margin; arista slightly pubescent; facial ridge devoid of bristles; ocellar bristles weak to absent; inner vertical bristles elongate, parallel, in some cases indistiguishable from upper frontal bristles; outer orbitals weak to absent in males, but strong in females; females with two pairs of proclinate orbital bristles.
Thorax: chaetotaxy as follows: postsutural supra-alar bristles 3 (2 in U. pannosa sp. nov.); acrostichal bristles 2:3; dorsocentral bristles 3:3 (4 in U. venusta); postpronotal bristles 4 or 5; two strong scutellar marginal bristles (except 3 in U. brevicauda); apical scutellar bristles long and decussate; 2–3 katepisternal bristles; propleuron bare; wings smoky gray, in some species with brown markings or bicolored: yellow at base and brownish-black distally; calypters broad, of yellow-amber color, haired marginally; legs black; claws and pulvilli elongate in males.
Abdomen: narrowed and elongate, at least twice as long as wide; frequently acutely produced dorsally into a tail-like process; mid-dorsal depression on ST1+2 reaching hind margin of syntergite; T3, T4 and sometimes ST1+2 with one to three pairs of discal bristles; all tergites with marginals. In females, abdomen usually not as elongate as males and with a rounded posterior end.
Uramya is easily distinguished by the following combination of traits: densely haired eyes; facial carina absent; facial ridge bare; parafacial bare (sometimes with a few black setulae in females); ocellar bristles weak to absent; prosternum bare; postpronotum with 4–5 bristles; 3 postsutural supra-alar bristles (2 in U. pannosa); 3 large postsutural dorsocentral bristles (4 in U. venusta); metathoracic spiracle fringed with plumose hairs of about equal size along anterior and posterior edges, leaving a V-shaped mid-dorsal opening; scutellum with 3–4 pairs of strong marginal scutellar bristles (1 pair of basal scutellar bristles, 1–2 pairs of lateral bristles, and 1 pair of subapical bristles), excluding a pair of strong, crossed apicals; vein M sharply angled at bend; abdomen subcylindrical (in males often with T5 dorsally produced into a tail-like structure), with 1–2 pairs of median discal bristles on tergites 3 and 4.
Nearctic and Neotropical (not known from Chile and southern Argentina)
According to
Male (Fig.
Female (Fig.
Uramya albosetulosa can be distinguished from all other Neotropical species of Uramya by the following combination of traits: dark brown to black antennae, 3 postsutural supra-alar bristles, underside of scutellum with a tuft of white hairs near basal marginal bristle, 1 pair of median marginal bristles on ST1+2 and T3; T4 and T5 with a row of marginal bristles; underside of abdomen pale pilose and silver pollinose.
The specific epithet is derived from the Latin adjective “ albus ”, for white, and the noun “ seta ”, for bristle, in reference to the tuft of white hairs present along the underside of the scutellum in this species.
Costa Rica, ACG (Guanacaste and Alajuela Provinces), 340–600 m.
Uramya albosetulosa sp. nov. has been reared 35 times from Acharia sarans (Dyar), Acharia hyperoche Dognin and Acharia apicalis (Dyar) (Limacodidae), from 2,035 wild-caught mixed siblings and non-siblings found in both dry and rain forest.
Male (Fig.
Female (Fig.
Uramya constricta can be distinguished from all other Neotropical species of Uramya by the following combination of traits: pedicel dark brown, 3 postsutural supra-alar bristles, underside of scutellum with a tuft of black hairs near basal marginal bristle, only 1 pair of median marginal bristles on ST1+2, T3 and T4, and by the shape of the surstylus.
The specific epithet is derived from the Latin adjective “constrictus”, for constricted or compressed, in reference to the slightly constricted base of ST1+2 where it meets the thorax.
Costa Rica, ACG (Prov. Guanacaste), 1,150 m.
Uramya constricta has been reared 38 times from Acharia ophelians Dyar (Limacodidae) (one sibling brood of caterpillars) and once from Euclea mesoamericanaDHJ04 (Lepidoptera: Limacodidae) in ACG cloud forest.
Male (Fig.
Female (Fig.
Uramya contraria can be distinguished from all other Neotropical species of Uramya by the following combination of traits: dark brown to black antennae, 3 postsutural supra-alar bristles, 2 strong lateral scutellar bristles, no discal scutellar bristles, underside of scutellum with a tuft of white hairs near basal marginal bristle, abdomen flattened dorsoventrally, ST1+2 with lateral white pollinose spots on either side of mid-dorsal depression, T5 subtriangular, not strongly produced into a long, tail-like process, 1 pair of median discal bristles on T3, T4 and T5, and silver pollinosity on underside of abdomen.
The species epithet is derived from the latin adjective " contrarius " for contrary or opposed, referring to its overall similarity but differing terminalia to U. halisidotae.
Costa Rica, ACG (Prov. Guanacaste), 440–520 m.
Uramya contraria has been reared four times from a sample of 100 wild-caught, non-sibling Caviria regina Cramer (Erebidae, Lymantriinae) in ACG rain forest.
Male (Fig.
Female: Unknown.
Uramya infracta can be distinguished from all other Neotropical species of Uramya by the following combination of traits: dark brown to black antennae with only a slight orange tinge and dark brown pedicel, thorax with black hairs interspersed among the bristles dorsally, and yellow-white hairs on sides and ventrally, underside of scutellum with a tuft of black hairs near basal marginal bristle, 1 pair of median marginal bristles on ST1+2, and a row of marginal bristles on T3 and T4.
The species epithet is derived from the latin adjective " infractus " meaning broken or weakened, in reference to the broken band of silver pollinosity on T5, which appears as two pollinose spots.
Costa Rica, ACG (Prov. Guanacaste), 900 m.
Uramya infracta has been reared only once, from a total of 153 wild-caught non-sibling Natada fusca Druce (Limacodidae) caterpillars in ACG rain forest.
Male (Fig.
Female (Fig.
Uramya lativittata can be distinguished from all other Neotropical species of Uramya by the following combination of traits: dark brown to black antennae, 3 postsutural supra-alar bristles, underside of scutellum with a tuft of black hairs near basal bristle, 4–5 pairs of marginal scutellar bristles, and silver pollinosity on underside of abdomen.
The species epithet is derived from a combination of the latin nouns " latus ", meaning side, and " vitta ", meaning band, in reference to its distinctive abdominal pattern.
Costa Rica, ACG (Provs. Guanacaste and Alajuela), 280–700 m.
Uramya lativittata has been reared 23 times from large caterpillars belonging to the genera Norape Walker, Megalopyge Hübner, Podalia Walker and Trosia Hübner (Megalopygidae) in a sample of 2,816 non-siblings from dry, rain and dry-rain intergrade forest.
Male (Fig.
Female: Unknown.
Uramya lunula can be distinguished from all other Neotropical species of Uramya by the following combination of traits: dark brown to black antennae, 3 postsutural supra-alar bristles, 2 strong lateral scutellar bristles, weak discal scutellar bristles, underside of scutellum with a tuft of black hairs near basal marginal bristle, abdomen flattened dorsoventrally, ST1+2 lacking silver pollinose spots on either side of mid-dorsal depression, T5 subtriangular, not strongly produced into a long, tail-like process, 2 pairs of median discal bristles on T3, T4 and T5, and silver pollinosity on underside of abdomen.
The species epithet is derived from the Latin noun “lunula”, for little moon, in reference to the crescent-shaped markings present on the abdomen of this species.
Costa Rica, ACG (Prov. Guanacaste), 405 m.
Uramya lunula has been reared only once, from a Podalia orsilocha (Cramer) (Megalopygidae) caterpillar found in ACG rain forest. Podalia orsilocha has been reared 175 times from sibling and non-sibling groups in ACG.
Male (Fig.
Female (Fig.
Uramya nitida can be distinguished from all other Neotropical species of Uramya by the following combination of traits: light-colored, orange-brown antennae, 2 postsutural supra-alar bristles, underside of scutellum with a tuft of black hairs near basal marginal bristle, 1 pair of median marginal bristles on ST1+2, and a row of marginal bristles on T3 and T4.
Uramya nitida is derived from the Latin noun "nitidus", meaning bright or glossy, in reference to the glossy appearance of the abdomen under certain angles of light.
Costa Rica, ACG (Prov. Guanacaste), 660–1220 m.
Uramya nitida has been reared 18 times from Parasa sandrae Corrales & Epstein (Limacodidae), in a sample of 497 non-sibling, wild-caught larvae in both cloud and rain forest.
Male (Fig.
Female (Fig.
Uramya pannosa can be distinguished from all other Neotropical species of Uramya by the following combination of traits: pedicel orange, 2 postsutural supra-alar bristles, underside of scutellum with a tuft of black hairs near basal marginal bristle, overall absence of abdominal hairs, only 1 pair of median marginal bristles on ST1+2, and 2 pairs of median discal bristles on T3 and T4.
The species epithet is derived from the Latin adjective “ pannosus ”, meaining tattered or shabby, in reference to the irregular and ragged appearance of the abdominal banding.
Costa Rica, ACG (Prov. Guanacaste), 900–1220 m.
Uramya pannosa has been reared 5 times from Parasa macrodonta Hering & Hopp (Limacodidae) in both cloud and rain forest, and is the only species of tachinid to have been reared from this species of caterpillar in 166 non-sibling rearings.
Male (Fig.
Female: Unknown.
Uramya penicillata is distinguished from all other Neotropical species of Uramya by the following combination of traits: light colored pedicel, 3 postsutural supra-alar bristles, the first of which is 4X smaller than the second, underside of scutellum with a tuft of black hairs near basal marginal bristle, rows of marginal bristles on T3 and T4, and transverse bands of silver pollinosity extending across tergites to underside of abdomen.
The species epithet is derived from the Latin noun “penicillus”, for paintbrush, in reference to the brush-like tuft of hairs present along the underside of the scutellum in this species.
Costa Rica, ACG (Prov. Guanacaste), 1460 m
Uramya penicillata has been reared only once, from an Isochaetes dwagsi Corrales & Epstein (Limacodidae) caterpillar found in cloud forest. Isochaetes dwagsi has been reared 503 times from sibling and non-sibling groups in ACG.
Male (Fig.
Female: no female specimen was available to us for study.
Uramya sibinivora can be distinguished from all other Neotropical species of Uramya by the following combination of traits: conspicuous white pilosity covering the katepisternum, meron, and anepimeron, ventral surface of abdomen, dorsum of the thorax, scutellum white pilose, only one pair of median discal bristles on T3, and the shape of the surstylus.
Costa Rica: ACG (Provs. Alajuela and Guanacaste), 280–1,080 m; Paraguay: Guairá, Villarica; Venezuela: Edo. Nueva Esparta, El Valle.
Within the context of the ACG inventory, Uramya sibinivora has been reared 6 times from Parasa wellesca Dyar and Euclea mesoamericana Corrales & Epstein (Limacodidae).
Revised key to the males of Uramya Robineau-Desvoidy of Central and South America This key builds on the work accomplished by |
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1 | Thorax either yellow-white or black pilose dorsally; katepisternum, meron, anepimeron, and ventral surface of abdomen yellow-white pilose | 2 |
– | Thorax black pilose dorsally; katepisternum, meron and anepimeron black pilose; ventral surface of abdomen black pilose | 11 |
2 | Dorsum of thorax and scutellum yellow-white pilose, matching sides and ventral surface of abdomen; postpronotum and anepisternum with fine, yellow-white hairs | 3 |
– | Dorsum of thorax and scutellum black pilose, contrasting with white pilose sides of thorax and ventral surface of abdomen | 5 |
3 | 2 pairs of median discals on T3, and a row of median marginals on T4; surstyli slender | U. plaumanni Guimarães |
– | Only 1 pair of median discals on T3 and T4; surstyli falciform | 4 |
4 | Abdomen cylindrical and elongate, narrower than thorax at basein dorsal view; surstyli long and scythe-like; 2 katepisternal bristles; row of marginal bristles on T3 and T4 | U. sibinivora Guimarães |
– | Abdomen subtriangular, at base in dorsal view; surstyli uniformly wide, tapering to a pointed tip; 3 katepisternal bristles; 1 pair of marginal bristles on T3 and T4 | U. insolita Guimarães |
5 | First postusutural supra-alar bristle absent; median marginal bristles only on ST1+2; two pairs of median discals on T3 and T4 | U. pannosa sp. nov. |
– | Three postsutural supra-alar bristles; median marginal bristles present on all tergites; one or two pairs of discal bristles on T3 and T4 | 6 |
6 | Pedicel orange | 7 |
– | Pedicel dark brown | 9 |
7 | One pair of median marginals on ST1+2, T3 and T4; femora of dark ground color, covered in gray pollinosity; tibiae of yellow or dark brown ground color | U. penicillata sp. nov. |
– | One pair of median marginals on ST1+2, an incomplete row of marginal bristles on T3, T4 and T5; legs of yellow ground color, covered in black hairs; coxae orange | 8 |
8 | Sides of thorax and underside of abdomen densely pilose; legs conspicuously yellow, thinly dark haired; T3 and T4 densely covered in erect hairs more than half as long as discal bristles; T5 lacking row of discal bristles. | U. setiventris (Wulp) |
– | Sides of thorax and underside of abdomen moderately pilose; legs densely covered in dark hair, making them appear brown; T3 and T4 densely covered in appressed hairs not more than 1/3 as long as discal bristles; row of discal bristles present on T5. | U. nitida sp. nov. |
9 | 3katepisternal bristles | U. infracta sp. nov. |
– | 2katepisternal bristles | 10 |
10 | ST1+2 with gray pollinosity dorsolaterally; underside of scutellum with a tuft of black hairs near basal marginal bristle; ST1+2 with 2 strong median marginal bristles and a row of weaker marginal bristles, extending to lateral marginal bristles; T3 and T4 with a row of marginal bristles | U. constricta sp. nov. |
– | Abdominal ST1+2 lacking gray pollinosity dorsolaterally; only one pair of median marginals on each of ST1+2 and T3, and T4 with a row of marginal bristles; underside of scutellum with a tuft of white hairs near basal marginal bristle | U. albosetulosa sp. nov. |
11 | Wings yellow along base, brown on outer costal portion; calypters strongly infuscate | 12 |
– | Wings brownish costobasally; calypters pale yellow to white, not strongly infuscate | 18 |
12 | ST1+2, T3, T4, and T5 segments with conspicuous patches of white pollinosity dorsolaterally | U. octomaculata (Townsend) |
– | At most 3 of the 5 visible abdominal segments with conspicuous patches of white pollinosity dorsolaterally or abdomen devoid of white pollinosity. | 13 |
13 | Abdomen completely devoid of white pollinosity | U. umbratilis (Reinhard) |
– | Abdomen with patches of white pollinosity | 14 |
14 | Abdomen with tergal banding broken into distinct, white pollinose patches on ST1+2, T3 and T4; T5 testaceous pollinose | U. quadrimaculata (Macquart) |
– | Abdomen with tergal banding broken into distinct, white pollinose patches on T3–T5, ST1+2 bare. | 15 |
15 | Thorax with greenish-gold pollinosity | U. penai (Guimarães) |
– | Thorax with grayish-white pollinosity | 16 |
16 | Wing with strongly contrasting colors: yellow along basal 1/3 and brown on outer 2/3 of costal portion; abdomen reddish-black with white pollinosity along sides of tergites | U. indita (Walker) |
– | Wing coloration not strongly contrasting; abdomen not distinctly reddish black, lacking white pollinosity on sides of tergites | 17 |
17 | Abdominal T5 sharply pointed; thorax with 3 katepisternal bristles and 3 postsutural dorsocentrals; wing coloration overall very faint, pale yellow at base and with costal portion faintly brown | U. acuminata (Wulp) |
– | Abdominal T5 broadly rounded; thorax with 2 katepisternal bristles and 4 postsutural dorsocentrals; wing bright yellow at base, with brown costal region | U. venusta (Wulp) |
18 | Abdominal T3 and T4 with a continuous transverse band of white pollen on anterior 1/4, fading towards apex; T5 not pollinose | U. nitens (Schiner) |
– | Abdominal T3 and T4 with thick silver pollen on sides, broken by a longitudinal dorsocentral stripe, present on basal 2/3 or less; T5 pollinose | 19 |
19 | T5 uniformly brown pollinose | U. townsendi Guimarães |
– | T5 brownish pollinose from middle to apex, white pollinose on sides | 20 |
20 | Scutellum uniformly white pollinose, bearing at least two strong lateral bristles and at least two pairs of discal bristles | 21 |
– | Scutellum brownish pollinose on anterior half, with two strong lateral bristles and discal bristles weak to absent (if discals are present, they are almost indistinct from surrrounding hairs) | 22 |
21 | Two strong, distinct discal scutellar bristles; anatergite bare | U. brevicauda (Curran) |
– | Discal scutellar bristles almost indistinct, appearing as thickened scutellar hairs; anatergite with a small patch of black hairs | U. lativittata sp. nov. |
22 | Abdominal T4 bearing a distinct ventrolateral tuft of hairs. | U. fasciata (Macquart) |
– | Abdominal T4 with hairs uniform in length. | 23 |
23 | Abdomen cylindrical; T5 elongated into a long tail-like process, at least 2–3X as long as T4; T3 with a pair of strong, median discal bristles; arista long and pubescent on basal half | U. producta Robineau-Desvoidy |
– | Abdomen more or less flattened dorsoventrally; T5 not produced into a long, tail-like process; if pointed, then less than 2–3X as long as T4; arista bare to minutely pubescent on basal half | 24 |
24 | Ventral surface of abdomen yellow-white pilose | U. longa (Walker) |
– | Ventral surface of abdomen black pilose | 25 |
25 | Abdominal ST1+2 bearing silver pollinose spots, lacking silver pollinosity along posterior margin; wing veins strongly infuscate, giving a dark grey tonality to the leading edge of the wing. | U. contraria sp. nov. |
– | Abdominal ST1+2 lacking silver pollinose spots, but with a thin transverse band of silver pollinosity along posterior margin; wing veins not strongly infuscate, infuscation only visible on basal halves of R4+5 and M. | U. lunula sp. nov. |
Fig.
Neighbor Joining tree (NJ –
We gratefully acknowledge the unflagging support of the team of ACG parataxonomists (Janzen et al. 2009, Janzen & Hallwachs 2011) who found and reared the specimens used in this study, and the team of biodiversity managers who protect and manage the ACG forests that host these tachinids and their caterpillar hosts. The study has been supported by U.S. National Science Foundation grants BSR 9024770 and DEB 9306296, 9400829, 9705072, 0072730, 0515699, and grants from the Wege Foundation, International Conservation Fund of Canada, Jessie B. Cox Charitable Trust, Blue Moon Fund, Guanacaste Dry Forest Conservation Fund, Area de Conservación Guanacaste, Permian Global, and University of Pennsylvania (DHJ & WH), and in-kind support from INBio and the Museo Nacional de Costa Rica. This study has also been supported by the Government of Canada through its ongoing support of the Canadian National Collection, Genome Canada, the Biodiversity Institute of Ontario, and the Ontario Genomics Institute (2008–0GI–ICI–03) (MAS), and by a Discovery Grant from Natural Sciences and Engineering Research Council of Canada (MAS).