Biodiversity Data Journal :
Taxonomic Paper
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Corresponding author: AJ Fleming (ajfleming604@gmail.com)
Academic editor: Pierfilippo Cerretti
Received: 08 Oct 2019 | Accepted: 21 Apr 2020 | Published: 28 Apr 2020
© 2020 AJ Fleming, D. Monty Wood, M. Alex Smith, Tanya Dapkey, Winnie Hallwachs, Daniel Janzen
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 DM, Smith MA, Dapkey T, Hallwachs W, Janzen D (2020) Revision of Telothyria van der Wulp (Diptera: Tachinidae) and twenty-five new species from Area de Conservación Guanacaste in northwestern Costa Rica with a key to Mesoamerican species. Biodiversity Data Journal 8: e47157. https://doi.org/10.3897/BDJ.8.e47157
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We describe 25 new species in the genus Telothyria van der Wulp, 1890 from Area de Conservación Guanacaste (ACG) in northwestern Costa Rica. All species herein described were reared from an ongoing inventory of wild-caught caterpillars spanning two families (Lepidoptera: Crambidae, and Tortricidae). Our study provides a concise description of each new species using morphology, life history, molecular data, and photographic documentation; a redescription of the genus, and its type species as well as a revised key to species of Telothyria occurring in the Mesoamerican region. We also suggest seven new synonymies resulting in 11 new combinations.
The following 25 new species of Telothyria are described: T. aidani sp. n., T. alexanderi sp. n., T. auranticrus sp. n., T. auriolus sp. n., T. bicuspidata sp. n., T. carolinacanoae sp. n., T. clavata sp. n., T. cristata sp. n., T. diniamartinezae sp. n., T. duniagarciae sp. n., T. duvalierbricenoi sp. n., T. eldaarayae sp. n., T. erythropyga sp. n., T. fimbriata sp. n., T. fulgida sp. n., T. gloriashihezarae sp. n., T. grisea sp. n., T. harryramirezi sp. n., T. incisa sp. n., T. manuelpereirai sp. n., T. obscura sp. n., T. omissa sp. n., T. osvaldoespinozai sp. n., T. peltata sp. n., and T. ricardocaleroi sp. n.
The following are proposed by Fleming & Wood as new generic synonyms of Telothyria: Comatacta Coquillett Syn. n., Floradalia Thompson Syn. n., Ptilomyia Curran Syn. n., Ptilomyiopsis Townsend Syn. n., Ptilomyoides Curran Syn. n., Euptilomyia Syn. n., Eutelothyria Townsend Syn. n.
The following new combinations are proposed as a result of the new synonymies: Telothyria bequaerti (Curran, 1925) Comb. n., Telothyria cruenta (Giglio-Tos, 1893) Comb. n., Telothyria frontalis (Townsend, 1939) Comb. n., Telothyria insularis (Curran, 1927) Comb. n., Telothyria itaquaquecetubae (Townsend, 1931) Comb. n., Telothyria major (Thompson, 1963) Comb. n., Telothyria micropalpus (Curran, 1925) Comb. n., Telothyria minor (Thompson, 1963) Comb. n., Telothyria nautlana (Townsend, 1908) Comb. n., Telothyria plumata (Curran, 1925) Comb. n., Telothyria trinitatis (Thompson, 1963) Comb. n., Telothyria variegata (Fabricius, 1805) Comb. n. Musca tricincta Fabricius is synonymized under Telothyria variegata Fabricius, Syn. n.
Telothyria schineri Fleming & Wood nom. n. is proposed as a replacement name for Miltogramma brevipennis Schiner.
Additionally we provide redescriptions of two previously named species: the type species Telothyria cupreiventris (van der Wulp) due to its being the type species, and Telothyria relicta (van der Wulp) due to its having been reared as an outcome of the inventory.
tropical rain forest, tropical dry forest, cloud forest, parasitoid flies, host-specificity, caterpillars, ACG, Dexiinae, Telothyriini
The Neotropical genus Telothyria
Our goal is to systematically revise and analyze the known members of the New World tachinid genus Telothyria van der Wulp (Dexiinae: Telothyriini). The tribe Telothyriini is distributed almost exclusively within the Neotropical region, except for one species from North America. The vast tachinid fauna of the Neotropical region, along with the huge number of genera, has proven to be one of the largest hurdles to understanding the generic boundaries within the Telothyriini, and properly understanding Neotropical Tachinidae.
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 25 new species of Telothyria are based on differences in external morphology, COI (coxI or cytochrome c oxidase I) gene sequences, and male terminalia (whenever possible). As the inventory is continually growing, this paper should not be taken as an indication of the final total number of species of Telothyria present in Costa Rica or even within ACG. While our key is comprehensive across the Mesoamerican range (also inclusive of several species from the Antilles), our descriptions are limited to a redescription of the type species, and the species known and reared from ACG to date. This paper on Telothyria 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 (
The management of voucher specimens has been detailed in previous papers in this series (
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. Unless otherwise noted the primary type material of the species newly described herein are all deposited in the CNC.
Species accounts and 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
Landmarks and salient features of Telothyria anatomy; a: lateral view of terminalia of Telothyria manuelpereirai sp. n.; b: dorsal view of terminalia of T. manuelpereirai; c: ventral view of sternite 5 T. relicta van der Wulp, 1890; d–e: detail of different meral hair types.
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 "Phostria Janzen52" or "Desmia benealisDHJ03", 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 sequences derived from a standardized 5’ region of the mitochondrial cytochrome c oxidase I (COI) gene were obtained for all ACG inventoried specimens using DNA extracts prepared from single legs using a modified glass fibre protocol (
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
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
NHMW, Naturhistorisches Museum Wien, Vienna, Austria
USNM, United States National Museum of Natural History, Washington, D.C., USA
ZMUC, Natural History Museum of Denmark, Zoological Museum, Copenhagen, Denmark
Telothyria van der Wulp, 1890: 44, [also 1890: 167]. Type species: Telothyria cupreiventris van der Wulp, 1890, by subsequent designation of Brauer & Bergenstamm (1891: 378 [also 1891: 74]).
Thereuops Brauer & Bergenstamm, 1891: 378 [also 1891: 74]. Type species: Miltogramma brevipennis Schiner, 1868 (preocc. by Miltogramma brevipennis Bigot, 1861), by subsequent designation of Brauer & Bergenstamm (1891: 378 [also 1891: 74]). Synonymy proposed by
Therevops. Incorrect subsequent spelling of Thereuops Brauer & Bergenstamm, 1891 (
Thelothyria. Incorrect subsequent spelling of Telothyria van der Wulp, 1890 (Brauer & Bergenstamm 1893: 132 [also 1893: 44]).
Comatacta Coquillett, 1902: 199. Type species: Brachycoma pallidula van der Wulp, 1890 (= Stomoxys variegata Fabricius, 1805), by original designation. Syn. n.
Leskiopsis Townsend, 1916: 627. Type species: Myiobia thecata Coquillett, 1895, by original designation. Synonymy proposed by
Ptilomyia Curran, 1925: 8 (preocc. by Ptilomyia Coquillett, 1910). Type species: Ptilomyia plumata Curran, 1925, by original designation. Synonymy proposed by
Ptilomyoides Curran, 1928: 112. Type species: Ptilomyia becquaerti Curran, 1925, by monotypy. Syn. n.
Eutelothyria Townsend, 1931: 332. Type species: Eutelothyria itaquaquecetubae Townsend, 1931, by original designation. Syn. n.
Ptilomyiopsis Townsend, 1933: 527 (nomen novum for Ptilomyia Curran). Type species: Ptilomyia plumata Curran, 1925, by designation of the same species for Ptilomyia Curran, 1925. [
Euptilomyia Townsend, 1939: 451. Type species: Euptilomyia frontalis Townsend, 1939, by original designation. Syn. n.
Floradalia Thompson, 1963: 486. Type species: Floradalia major Thompson, 1963, by original designation. Syn. n.
Other species included in Telothyria Robineau-Desvoidy
bequaerti Curran, 1925: 352 (Ptilomyia). Holotype male (AMNH), by original designation. Type locality: Brazil, Roraima, San Alberto. [Type locality cited in
brasiliensis Townsend, 1929: 369 (Leskiopsis). Holotype female (USNM). Type locality: Brazil, São Paulo, Itaquaquecetuba.
cruenta Giglio-Tos, 1893: 3 (Chaetona). Holotype female (MRSN), by original designation. Type locality: Mexico. Comb. n.
cupreiventris van der Wulp, 1890: 169 in key [1890: 182, description] (Telothyria). Lectotype male [not female as published,
frontalis Townsend, 1939: 451 (Euptilomyia). Syntypes, 2 males (USNM), by original designation. Type locality: Brazil, São Paulo, Juquía [cited in
illucens van der Wulp, 1890: 169 [also 1890: 183] (Telothyria). Syntypes, 3 males and 2 females (3 in BMNH). Type locality: Mexico, Tabasco, Teapa.
insularis Curran, 1927: 12 (Comatacta). Holotype male (AMNH), by original designation. Type locality: Puerto Rico, San Juan. Comb. n.
itaquaquecetubae Townsend, 1931: 333 (Eutelothyria). Holotype male (USNM), by original designation. Type locality: Brazil, São Paulo, Itaquaquecetuba Comb. n.
major Thompson, 1963: 486 (Floradalia). Holotype female (CNC), by original designation. Type locality: Trinidad, Maracas Valley. Comb. n.
micropalpus Curran, 1925: 9 (Ptilomya). Holotype male (AMNH), by original designation. Type locality: Brazil, “Piedra Blanca” (as “Chapada”, in error according to
minor Thompson, 1963: 488 (Floradalia). Holotype male (CNC), by original designation. Type locality: Trinidad, St. Augustine. Comb. n.
nautlana Townsend, 1908: 101 (Comatacta). Holotype male [sex not given in original description, determined from holotype examination] (USNM), by original designation. Type locality: Mexico, Veracruz, San Rafael, Jicaltepec. Comb. n.
placida van der Wulp, 1890: 169 [also 1890: 182] (Telothyria). Holotype female (BMNH). Type locality: Mexico, Tabasco, Teapa.
plumata Curran, 1925: 8 (Ptilomya). Lectotype male (AMNH), designated by Arnaud (1963). Type locality: Brazil, Mato Grosso, "Chapada" [probably in or near present-day Parque Nacional da Chapada dos Guimarães]. Comb. n.
relicta van der Wulp, 1890: 171 (Telothyria). Holotype female (BMNH). Type locality: Mexico, Veracruz, Atoyac.
rufopygata Bigot, 1889: 262 (Viviana, as "V.? rufopygata"). Holotype female (BMNH). Type locality: Mexico.
rufostriata van der Wulp, 1890: 172 (Telothyria). Syntypes, 1 male and 1 female (BMNH). Type locality: Mexico, Veracruz (Atoyac) and Tabasco (Teapa).
schineri Fleming & Wood, nom. n. for Miltogramma brevipennis Schiner, 1869
brevipennis Schiner, 1868: 324 (Miltogramma). Holotype male (NHMW). Type locality: Brazil. Junior primary homonym of Miltogramma brevipennis
thecata Coquillett, 1895: 105 (Myiobia). Lectotype male (USNM), by fixation of Townsend in
trinitatis Thompson, 1963: 484 (Eutelothyria). Syntypes males and females (1 male in CNC), by original designation. Type locality: Trinidad, Brazil (village name). Comb. n.
variegata Fabricius, 1805: 281 (Stomoxys). Holotype male (ZMUC), by original designation. Type locality: South America. Comb. n.
tricincta Fabricius, 1805: 301 (Musca). Holotype female (ZMUC). Type locality: South America. Syn. n.
pallidula van der Wulp, 1890: 95 (Brachycoma). Holotype male (BMNH). Type locality: Mexico, North Yucatan, Temax.
Male. Head: frons narrow 1/10-1/8 of head width; 1–4 reclinate orbital setae; anteriormost reclinate orbital seta distinctly longer than uppermost frontal seta; ocellar setae most often absent, if present then these appearing short and underdeveloped, easily confused with vertical setulae arising behind anterior ocellus; eye bare, ventral margin below level of vibrissa; fronto-orbital plate ranging from shining silver or gold to brownish with a silver sheen; fronto-orbital plate with short black or blonde hairs interspersed among frontal setae; fronto-orbital plate with setae not extending below lower margin of pedicel; lower margin of face slightly lower than vibrissa almost not visible in profile; facial ridge bare in most species, the few exceptions possessing yellow almost inconspicuous hairs along margin; palpus either straight or with a slight club at apex, sparsely haired; arista ranging from bare to plumose, usually distinctly-thickened on basal 1/2, ranging in color from orange to dark brown-black. Thorax: gray to golden tomentose over a black to reddish-brown ground color; thorax covered in dense plumose blonde hairs or plumose hairs confined to lateral surfaces with disc of scutum covered in thin black hairs; prosternum bare; chaetotaxy: one proepimeral seta; one proepisternal seta; 4–5 postpronotal setae, basal setae arranged in a straight line; supra-alar setae 1–2:3; intra-alar setae 1–2:2–3; dorsocentral setae 3–4:3–4; acrostichal setae 3–4:3–4; katepisternum with 2–3 setae; meral setae usually absent in the traditional sense instead meral row replaced by a fan of long plumose hairs (Fig.
Female as in male except in the following aspects: head: bearing 2–3 pairs of proclinate orbital setae, as well as 2–3 pairs of reclinate inner orbital setae; one pair of outer vertical setae present; thorax: meron bearing either typical meral setae not plumose blonde hairs as in male (Fig.
Telothyria can be recognized most easily by the presence of long plumose hairs covering more than 50% of the thoracic surfaces, a trait that was historically used to unify the genera within the tribe. In males of the genus, and many of the females, the meral setae are also replaced with these plumose hairs. Characters of note within Telothyria are: prosternum bare; fronto-orbital plate haired; parafacial bare; arista ranging from plumose to bare; ocellar setae weakly developed or absent; eye bare; females of all species with two pairs of well-developed proclinate orbital setae, absent in males; first postsutural supra-alar seta poorly developed in length at most 0.5X second postsutural supra-alar; the three major setae of the postpronotum arranged in a straight line; most of the thorax covered in plumose blonde or coppery hairs (some species lack these setae dorsally) (Fig.
From southeastern USA west to Mexico and south to Brazil.
Within the ACG inventory Telothyria has been reared from two families of lepidopteran hosts throughout the diverse ecosystems of the research area, Crambidae, and Tortricidae.
Based on our observations of the apomorphies shared by the species assigned to the tribe Telothyriini, expressed as a result described herein, we propose the synonymy of all the genus-group names listed above within the tribe Telothyriini. Most recently, it has been suggested that the Telothyriini are a phylogenetically nested sub-clade within the Dexiinae (
Male. Length: 5–9 mm (Fig.
Female. Length: 5–7 mm (Fig.
Telothyria aidani sp. n. can be distinguished from all other Telothyria by the following combination of traits: ocellar setae absent, parafacial pale silver, postpedicel entirely orange, arista plumose on lower half with microtrichia at most 3X as wide as arista, facial ridge bare, thorax entirely covered in dense plumose blonde hairs. Differs from T. alexanderi by ST1+2 brown over medial 50%, in females abdominal coloration overall darker than that of females of T. alexanderi, ground color brown dorsally on ST1+2 and T3 with orange laterally, and T4 entirely brown ground color. CO1 barcode differs from Telothyria alexanderi by 1%.
Telothyria aidani sp. n. the new species is named in honor of my second son Aidan José Fleming. Just as we honor those who have worked before us, we must also recognize the potential of those who might continue our work and carry our legacy into the future.
Costa Rica, ACG, Guanacaste Province, 85–305 m elevation.
Telothyria aidani sp. n. has been reared 11 times from two species of Lepidoptera in the family Crambidae: Herpetogramma Janzen04 and Spoladea recurvalis (Fabricius, 1775) in dry forest and dry-rain lowland intergrade.
Male. Length: 6 mm (Fig.
Female. Length: 6–8 mm (Fig.
Telothyria alexanderi sp. n. can be distinguished from all other Telothyria by the following combination of traits: ocellar setae absent, parafacial pale silver, postpedicel entirely orange, arista plumose on lower half with microtrichia at most 3X as long as width of arista, facial ridge bare, thorax entirely covered in dense plumose blonde hairs. Differs from T. aidani by ST1+2 brown over medial 30%, females generally lighter than those of T. aidani, with ground color orange entirely and a dorsocentral brown stripe along T3 and T4 and anterior 1/2 of T5. CO1 barcode differs from Telothyria aidani sp. n. by 1%.
Telothyria alexanderi sp. n. the new species is named in honor of my first son Alexander José Fleming, who inspires me everyday to continue to learn and strive to make this world a better place for the future.
Costa Rica, ACG, Guanacaste Province, 85–305 m elevation.
Telothyria alexanderi sp. n. has been reared five times from two species of Lepidoptera in the family Crambidae: Herpetogramma Janzen04 and Spoladea recurvalis in dry forest and dry-rain lowland intergrade.
Male. Length: 9–11mm (Fig.
Female. Unknown at this time.
Telothyria auranticrus sp. n. can be distinguished from all other Telothyria by the following combination of traits: frons narrow, fronto-orbital plate pale brassy-gold throughout, parafacial pale silver, two katepisternal setae, thorax entirely covered in dense plumose blonde hairs, sometimes sparse on disc of scutum, T4 entirely dark brown, and T5 orange with gold tomentum.
Telothyria auranticrus sp. n. From the Latin adjective, “aurantium” for orange and the noun "crus" for leg, in reference to its bright orange legs.
Mexico, Veracruz Province, Lake Catemaco; San Luis Potosi Province, Xilitila.
Specimens hand collected two times, further ecology not available.
Male. Length: 10 mm (Fig.
Female. unknown at this time.
Telothyria auriolus sp. n. can be distinguished from all other Telothyria by the following combination of traits: frons narrow, fronto-orbital plate silver throughout, parafacial pale silver, three katepisternal setae, two postsutural intra-alar setae, basicosta ivory white, thorax entirely covered in dense plumose blonde hairs, median marginal setae absent from T3.
Telothyria auriolus sp. n. From the Latin adjective, “auriolus” meaning made of gold, in reference to its overall light color and its brilliant yellow legs.
Mexico, Chiapas Province, Palenque Ruins; Honduras, Atlantida, 950 m elevation.
Specimens hand collected five times at high elevations, further ecology not available.
Male. Length: 8–10 mm (Fig.
Female. Unknown at this time.
Telothyria bicuspidata sp. n. can be distinguished from its congeners by the following combination of traits: frons narrow, fronto-orbital plate pale brassy-gold throughout, thorax covered in dense plumose blonde hairs throughout, two katepisternal setae, three postsutral intra-alar setae, wings slightly infuscate, calypters brassy brown, and median marginal setae present on ST1+2 and T3.
Telothyria bicuspidata sp. n. From the Latin prefix "bi-" meaning two, the noun, "cuspis" meaning tooth, and the suffix "ata" in reference to T5 resembling a pair of canine (cuspid) teeth.
Costa Rica, Puntarenas Province, Monteverde 1500 m elevation.
Specimens hand collected, six times from 1500 m, further ecology not available.
Female. Length: 6 mm (Fig.
Male. Unknown at this time.
Telothyria carolinacanoae sp. n. can be distinguished from all other Telothyria by the following combination of traits: ocellar setae absent, plumose blonde hairs absent from disc of scutum, katepisternum with three setae, two postsutural intra-alar setae, and T1+2–T4 with gold tomentum at tergal margin changing to silver tomentum extending over up to 50% of tergite, ground color mostly brown with yellow-orange present ventrolaterally.
Telothyria carolinacanoae sp. n. is named in recognition of Carolina Cano's outstanding work on the team that conducts the caterpillar and parasite inventory from ACG’s Estación Biológica San Gerardo.
Costa Rica, ACG, Guanacaste Province, 292m elevation.
Telothyria carolinacanoae sp. n. has been reared once from a single species of Lepidoptera in the family Crambidae: Herpetogramma phaeopteralis, in rain forest.
Male. Length: 10–11mm (Fig.
Female. Unknown at this time.
Very distinctive species of Telothyria can be distinguished from its congeners by the following combination of traits: ocellar setae absent, or apparently absent, fronto-orbital plate and parafacial pale brassy-gold, with four thick and distinct dorsal stripes, bearing a basal dark dorsomedial stripe on postsutural scutum directly adjacent to scutellum, plumose blonde hairs absent from disc of scutum, punctuated on anepisternum at base of postpronotum with a spot of long brown plumose hairs, dorsally thorax densely covered in black hairs, katepisternum with three setae, and entire abdomen bright orange.
Telothyria clavata sp. n. From the Latin noun, “clavus” for the stripes on the tunics of Roman senators, in reference to the uniquely bold dorsal stripes.
Costa Rica, Puntarenas Province, Monteverde 1400–1500 m elevation.
Specimens hand collected once, ecology not available.
Male. Length: 7–9 mm (Fig.
Female. Length: 5–7 mm (Fig.
Telothyria cristata sp. n. can be distinguished from all other Telothyria by the following combination of traits: ocellar setae absent, parafacial entirely gold, silvery–gray in females, postpedicel only 30% orange, directly adjacent to pedicel, thorax with only two outer stripes evident, plumose blonde hairs absent from disc of scutum, abdominal ground color dark maroon to blackish under certain angles of light, with dark orange lateroventrally from ST1+2–T5, and T5 maroon with silver tomentum. T. cristata differs from its closest congener T. cupreiventris Van der Wulp, by the presence of orange along the lateral surfaces of the abdomen in both males and females.
Telothyria cristata sp. n. From the Latin adjective “cristatum” meaning crested, in reference to the crest of hairs that line ST5 in the male terminalia.
Costa Rica, ACG, Alajuela Province, 360–500 m elevation.
Telothyria cristata sp. n. has been reared six times from six species of Lepidoptera in the family Crambidae: Pilemia Janzen42, Pilemia periusalis, Piletosoma thialis, Desmia benealisDHJ02, Herpetogramma Solis11 in dry forest, rain forest, and dry-rain lowland intergrade.
Telothyria cupreiventris van der Wulp, 1890: 169 in key [also 1890: 182 in description]. Lectotype male [not female as published, Townsend 1931: 91] (BMNH), by fixation of Townsend (1931: 91). Type locality: Mexico, Tabasco, Teapa.
Male. Length: 7–9 mm (Fig.
Female. Length: 5–7 mm (Fig.
Telothyria cupreiventris can be distinguished from all other Telothyria by the following combination of traits: ocellar setae absent, parafacial entirely gold, silvery–gray in the female, postpedicel only 30% dark burnt-orange, directly adjacent to pedicel, thoracic stripes truncated and only slightly evident, plumose hairs on thorax absent from disc of scutum, lateral plumose hairs reddish-brown mixed with blonde, abdominal ground color dark maroon appearing blackish under certain angles of light, without any traces of orange lateroventrally, and T5 with silver tomentum. Telothyria cupreiventris differs from T. cristata by the entirely maroon abdomen, and its reddish-brown plumose hairs present on lateral surfaces of thorax.
Mexico, Tabasco and Veracruz.
Ecology of Telothyria cupreiventris van der Wulp unknown.
Female. Length: 5 mm (Fig.
Male. Unknown at this time.
Telothyria diniamartinezae sp. n. can be distinguished from all other Telothyria by the following combination of traits: ocellar setae minimal but present, plumose hairs on thorax absent from disc of scutum, katepisternum with three setae, three postsutural intra-alar setae, legs with yellow coxa, T4 entirely dark brown, and T5 mostly dark brown with orange apically and covered in bronze-brown tomentum.
Telothyria diniamartinezae sp. n. is named in recognition of Dinia Martinez's outstanding work on the team that conducts the caterpillar and parasite inventory from ACG’s Estación Biológica Quica.
Costa Rica, ACG, Alajuela Province, 400 m elevation.
Telothyria diniamartinezae sp. n. has been reared once from a single species of Lepidoptera in the family Crambidae: Neoleucinodes Janzen02, in rain forest.
Male. Length: 8 mm (Fig.
Female. Length: 6 mm (Fig.
Telothyria duniagarciae sp. n. can be distinguished from all other Telothyria by the following combination of traits: ocellar setae absent, arista brown, with microtrichia at most 1.5X as long as width of arista, pedicel orange and postpedicel orange over 60% of surface, parafacial gold, silver in females, thorax covered in dense plumose blonde hairs laterally, plumose hairs on disc of scutum present yet sparse, and mixed in with short black hairs, katepisternum with three setae, legs yellow, abdominal ground color yellow-orange, and T5 yellow with silver tomentum.
Telothyria duniagarciae sp. n. is named in recognition of Dunia Garcia's outstanding work on the team that conducts the caterpillar and parasite inventory from ACG’s Estación Biológica Cacao.
Costa Rica, ACG, Alajuela and Guanacaste Provinces, 121–410 m elevation.
Telothyria duniagarciae sp. n. has been reared three times from two species of Lepidoptera in the families Crambidae and Depressariidae: Ategumia Solis01, and Filinota Janzen154 respectively, in rain forest.
Female. Length: 5 mm (Fig.
Male. Unknown at this time.
Telothyria duvalierbricenoi sp. n. can be distinguished from all other Telothyria by the following combination of traits: ocellar setae absent, fronto-orbital plate mostly silver, pale brassy-gold along upper third inclusive of ocellar triangle, plumose hairs on thorax absent from disc of scutum, thorax brassy-gold tomentose dorsally, grey laterally, katepisternum with three setae, legs dark reddish-brown, abdominal ground color yellow-orange, and T5 black marroon along anterior margin with yellow apically, entirely covered in silver tomentum. Differentiates from Telothyria insularis Curran with its entirely silver gena, the presence of four thin dorsal stripes on the thorax, and the color of the coxae.
Telothyria duvalierbricenoi sp. n. is named in recognition of Duvalier Briceño's outstanding work on managing the caterpillar and parasite inventory from his home and rearing barn in Brasilia, Alajuela Province. Costa Rica.
Costa Rica, ACG, Alajuela Province, 109 m elevation.
Telothyria duvalierbricenoi sp. n. has been reared once times from a single species of Lepidoptera in the family Crambidae: Salbia cassidalis (Guenée, 1854), in rain forest.
Male. Length: 6–7 mm (Fig.
Female. Length: 5 mm (Fig.
Telothyria eldaarayae sp. n. can be distinguished from all other Telothyria by the following combination of traits: ocellar setae present but minimal, plumose hairs absent from disc of scutum, katepisternum with three setae, two postsutural intra-alar setae, three postsutural intra-alar setae in females, and T5 yellow with silver tomentum. Can be distinguished from T. minor (Thompson) by the yellow ground color and tomentum present on the legs.
Telothyria eldaarayae sp. n. is named in recognition of Elda Araya’s outstanding work on the team that conducts the caterpillar and parasite inventory from ACG’s Estación Biológica San Gerardo.
Costa Rica, ACG, Alajuela Province, 123–461 m elevation.
Telothyria eldaarayae sp. n. has been reared six times from a single species of Lepidoptera in the family Crambidae: Salbia hameorrhoidalis Guenée, 1854, in rain forest.
Male. Length: 5–9 mm (Fig.
Female. Length: 5–7 mm (Fig.
Telothyria erythropyga sp. n. can be distinguished from all other Telothyria by the following combination of traits: ocellar setae present but so small as to appear absent, parafacial brilliant silver, postpedicel orange over at most 60% of surface, arista plumose microtrichia at most equally as long as width of arista, facial ridge bare, thorax entirely covered in dense plumose blonde hairs, and T5 orange with gold tomentum.
Telothyria erythropyga sp. n. From the Greek adjective “erythros” meaning red and the Greek noun "pygo" meaning rump or tail, in reference to the apically orange T5.
Costa Rica, ACG, Alajuela and Guanacaste Provinces, 320–540 m elevation.
Telothyria erythropyga sp. n. has been reared 33 times from four species of Lepidoptera in the family Crambidae: Phostria Janzen05, Phostria Janzen03, Desmia Solis19, Desmia Janzen576, Desmia Janzen07 in rain forest and dry-rain lowland intergrade.
Male. Length: 6–8 mm (Fig.
Female. Length: 6–8 mm (Fig.
Telothyria fimbriata sp. n. can be distinguished from all other Telothyria by the following combination of traits: ocellar setae present but minimal, parafacial brilliant silver, postpedicel almost entirely orange, arista plumose on lower half with microtrichia not exceeding the width of the arista, fine yellow hairs extending along at least lower half of facial ridge, thorax entirely covered in dense plumose blonde hairs, and T5 yellow with gold tomentum.
Telothyria fimbriata sp. n. From the Latin adjective “fimbriatus” meaning fringed in reference to the pale blonde hairs that line the facial ridge.
Costa Rica, ACG, Alajuela Province, 123–135 m elevation.
Telothyria fimbriata sp. n. has been reared eight times from a single species of Lepidoptera in the family Tortricidae: Phricanthes flexilineana (Walker, 1863), in rain forest.
Male. Length: 7–9 mm (Fig.