Telothyria Telothyria cupreiventris Thereuops Miltogramma brevipennis Miltogramma brevipennis Telothyria schineri Therevops Thereuops Thelothyria Telothyria Comatacta Brachycoma pallidula Stomoxys variegata Leskiopsis Myiobia thecata Ptilomyia Ptilomyia Ptilomyia plumata Ptilomyoides Ptilomyia becquaerti Eutelothyria Eutelothyria itaquaquecetubae Ptilomyiopsis Ptilomyia Ptilomyia plumata Ptilomyia Ptilomyia Comatacta Ptilomyia Ptilomyia plumata Comatacta Comatacta Euptilomyia Euptilomyia frontalis Floradalia Floradalia major Telothyria Telothyria bequaerti Ptilomyia Telothyria Leskiopsis cruenta Chaetona cupreiventris Telothyria frontalis Euptilomyia Telothyria Telothyria insularis Comatacta itaquaquecetubae Eutelothyria major Floradalia micropalpus Ptilomya minor Floradalia nautlana Comatacta Telothyria Telothyria plumata Ptilomya relicta Telothyria Telothyria Viviana Telothyria Telothyria schineri Miltogramma brevipennis brevipennis Miltogramma Miltogramma brevipennis Miltogramma brevipennis Miltogramma brevipennis Sarcophagidae Telothyria schineri Miltogramma brevipennis thecata Myiobia trinitatis Eutelothyria variegata Stomoxys tricincta Musca pallidula Brachycoma Telothyria Telothyria cupreiventris Revision of Telothyria van der Wulp (Diptera: Tachinidae) and twenty-five new species from Area de Conservacion Guanacaste in northwestern Costa Rica with a key to Mesoamerican species Fleming, AJ Wood, D. Monty Smith, M. Alex Dapkey, Tanya Hallwachs, Winnie Janzen, Daniel Biodiversity Data Journal 2020 8 47157 47157 95B4FE67-0487-5BED-AA7D-B795A869C8CB van der Wulp, 1890 van der Wulp 1890 Insecta Tachinidae Telothyria CoL Animalia Telothyria Diptera 0 47157 Arthropoda genus   Telothyriavan der Wulp, 1890: 44, [also 1890: 167]. Type species:  Telothyria cupreiventrisvan der Wulp, 1890, by subsequent designation of Brauer & Bergenstamm (1891: 378 [also 1891: 74]).  ThereuopsBrauer & Bergenstamm, 1891: 378 [also 1891: 74]. Type species:  Miltogramma brevipennisSchiner, 1868 (preocc. by  Miltogramma brevipennisBigot, 1861), by subsequent designation of Brauer & Bergenstamm (1891: 378 [also 1891: 74]). Synonymy proposed by Aldrich 1929:7. [see below under  Telothyria schineriFleming & Wood, nom. n.]  Therevops. Incorrect subsequent spelling of  ThereuopsBrauer & Bergenstamm, 1891 ( Aldrich 1929: 7, 33).  Thelothyria. Incorrect subsequent spelling of  Telothyriavan der Wulp, 1890 (Brauer & Bergenstamm 1893: 132 [also 1893: 44]).  ComatactaCoquillett, 1902: 199. Type species:  Brachycoma pallidulavan der Wulp, 1890 (=  Stomoxys variegataFabricius, 1805), by original designation. Syn. n.  LeskiopsisTownsend, 1916: 627. Type species:  Myiobia thecataCoquillett, 1895, by original designation. Synonymy proposed by Wood and Zumbado 2010: 1412.  PtilomyiaCurran, 1925: 8 (preocc. by  PtilomyiaCoquillett, 1910). Type species:  Ptilomyia plumataCurran, 1925, by original designation. Synonymy proposed by Curran 1928: 112.  PtilomyoidesCurran, 1928: 112. Type species:  Ptilomyia becquaertiCurran, 1925, by monotypy. Syn. n.  EutelothyriaTownsend, 1931: 332. Type species:  Eutelothyria itaquaquecetubaeTownsend, 1931, by original designation. Syn. n.  PtilomyiopsisTownsend, 1933: 527 ( nomen novumfor  PtilomyiaCurran). Type species:  Ptilomyia plumataCurran, 1925, by designation of the same species for  PtilomyiaCurran, 1925. [ Curran 1928proposed the synonymy of  PtilomyiaCurran, 1925 with  ComatactaCoquillett, 1902. Despite this proposed synonymy Townsend 1933proposed a replacement name for  PtilomyiaCurran, erected on the basis of  Ptilomyia plumataCurran, 1925 which Townsend considered to be generically distinct from  Comatacta; junior synonym of  ComatactaCoquillett, 1902 [ teste Curran 1928: 112]]. Syn. n.  EuptilomyiaTownsend, 1939: 451. Type species:  Euptilomyia frontalisTownsend, 1939, by original designation. Syn. n.  FloradaliaThompson, 1963: 486. Type species:  Floradalia majorThompson, 1963, by original designation. Syn. n.  Telothyria Other species included in  TelothyriaRobineau-Desvoidy  bequaertiCurran, 1925: 352 (  Ptilomyia). Holotype male (AMNH), by original designation. Type locality: Brazil, Roraima, San Alberto. [Type locality cited in Curran (1928)as Honduras in error] Comb. n.  Telothyria brasiliensis  Leskiopsis  cruentaGiglio-Tos, 1893: 3 (  Chaetona). Holotype female (MRSN), by original designation. Type locality: Mexico. Comb. n.  cupreiventrisvan der Wulp, 1890: 169 in key [1890: 182, description] (  Telothyria). Lectotype male [not female as published, Townsend 1931: 91] (BMNH), by fixation of Townsend 1931: 91. Type locality: Mexico, Tabasco, Teapa.  frontalisTownsend, 1939: 451 (  Euptilomyia). Syntypes, 2 males (USNM), by original designation. Type locality: Brazil, SaoPaulo, Juquia[cited in  Guimaraes1971: 121 as Itaquaquecetuba]. Comb. n.  Telothyria illucens  Telothyria  insularisCurran, 1927: 12 (  Comatacta). Holotype male (AMNH), by original designation. Type locality: Puerto Rico, San Juan. Comb. n.  itaquaquecetubaeTownsend, 1931: 333 (  Eutelothyria). Holotype male (USNM), by original designation. Type locality: Brazil, SaoPaulo, Itaquaquecetuba Comb. n.  majorThompson, 1963: 486 (  Floradalia). Holotype female (CNC), by original designation. Type locality: Trinidad, Maracas Valley. Comb. n.  micropalpusCurran, 1925: 9 (  Ptilomya). Holotype male (AMNH), by original designation. Type locality: Brazil, "Piedra Blanca" (as "Chapada", in error according to Arnaud 1963: 126). Comb. n.  minorThompson, 1963: 488 (  Floradalia). Holotype male (CNC), by original designation. Type locality: Trinidad, St. Augustine. Comb. n.  nautlanaTownsend, 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.  Telothyria placida  Telothyria  plumataCurran, 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 Guimaraes]. Comb. n.  relictavan der Wulp, 1890: 171 (  Telothyria). Holotype female (BMNH). Type locality: Mexico, Veracruz, Atoyac.  Telothyria rufopygata  Viviana V.? rufopygata  Telothyria rufostriata  Telothyria  schineriFleming & Wood, nom. n.for  Miltogramma brevipennisSchiner, 1869  brevipennisSchiner, 1868: 324 (  Miltogramma). Holotype male (NHMW). Type locality: Brazil. Junior primary homonym of  Miltogramma brevipennis Bigot 1861. [  Miltogramma brevipennis Schiner 1868is a junior primary homonym of  Miltogramma brevipennisBigot, 1861 a valid name within the Sarcophagidae. The authors hereby propose the replacement name  Telothyria schinerifor  Miltogramma brevipennisSchiner. The type material originally referenced by Schiner is conserved, with the specific epithet being selected in honor of Ignaz Rudolph Schiner.]  thecataCoquillett, 1895: 105 (  Myiobia). Lectotype male (USNM), by fixation of Townsend in Townsend 1939: 250 (mention of "Ht male" from Bucks and Delaware counties in USNM is regarded as a lectotype fixation). Type locality: USA, Pennsylvania, Bucks County.  trinitatisThompson, 1963: 484 (  Eutelothyria). Syntypes males and females (1 male in CNC), by original designation. Type locality: Trinidad, Brazil (village name). Comb. n.  variegataFabricius, 1805: 281 (  Stomoxys). Holotype male (ZMUC), by original designation. Type locality: South America. Comb. n.  tricinctaFabricius, 1805: 301 (  Musca). Holotype female (ZMUC). Type locality: South America. Syn. n.  pallidulavan der Wulp, 1890: 95 (  Brachycoma). Holotype male (BMNH). Type locality: Mexico, North Yucatan, Temax.  Telothyria Telothyria cupreiventrisvan der Wulp, 1890: 169. by subsequent designation  Description  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. 2 c). Scutellum with three pairs marginal setae; apical scutellar setae crossed apically, 1/8-1/10th as long as subapical scutellars; basal scutellar setae equal in length to subapical setae, often slightly shorter; subapical setae straight, ranging from divergent to convergent; ranging from gray to golden pollinose. Legs: ranging in ground color from yellow to dark reddish-brown; coxae covered in dense plumose blonde hairs. Wing: slightly longer than abdomen; translucent slightly hyaline; all veins bare, with 1-2 setula at base of vein R4+5; apical cell open at or just before the apex of wing; bend of vein M obtuse-angled. Abdomen: ground color ranging from a deep maroon, to different tonalities of yellow-orange with longitudinal middorsal brown markings; middorsal depression on syntergosternite 1+2 (ST1+2) reaching to hind margin of tergite; median marginal setae present only on tergite 4 (T4) and tergite 5 (T5) (one exception  Telothyria omissa sp. n., which lacks the marginal setae on tergite 4 (T4)); median discal setae absent on ST1+2-T4, occasionally present on T5; sex patch absent. Male terminalia: Sternite 5 with median cleft ranging from deeply excavated and smoothly V-shaped, to shallow and only slightly separated; margins either bare or covered in dense pollinosity; lateral lobes of sternite either sharply pointed, rounded apically or squared, sometimes with a small group of strong setulae along outer margins; basal section of sternite 5 subequal to slightly longer than length of apical lobes. Cerci in posterior view sharply pointed and triangular typically with a well defined basal shoulder separating upper lobe from apical section, ranging from slightly shorter to subequal in length of surstyli, fused along entire length; in lateral view, with a strong downward curve on apical 1/3, and several strong widely spaced setae along basal 2/3. Surstylus in lateral view, almost equilateral along its length, rounded at tip, sometimes slightly pinched at midpoint appearing digitiform, appearing fused with epandrium, when viewed dorsally straight and slender or with a slight sinusoidal curve, parallel at apices. Distiphallus either long and slender or short and stout, ranging from 1.5X to 2X as long as basiphallus and tubular, weakly tapering apically. Distiphallus, hinged at a strong acute angle with basiphallus, a synapomorphy of the Dexiinae.  Femaleas 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. 2 d) or a mix of both plumose blonde hairs and regular setae (Fig. 2 e); legs: can display dimorphic coloration from males; abdomen: slightly more globose than males, coloration of the abdomen can be dimorphic between the sexes; female terminalia were not dissected, however external examination showed these to be unspecialized.  Diagnosis   Telothyriacan 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  Telothyriaare: 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. 1); wings lacking costal spine. Abdomen with median marginal setae only on T4 and T5 (exception  Telothyria omissa sp. n.), and discal setae absent.  Distribution From southeastern USA west to Mexico and south to Brazil.  Ecology Within the ACG inventory  Telothyriahas been reared from two families of lepidopteran hosts throughout the diverse ecosystems of the research area, Crambidae, and Tortricidae.  Guimaraes(1977), suggested  Spodopterasp. of the family Noctuidae, however he failed to identify the species of  Telothyriaand as such casts a doubt on this potential host.  Taxon discussion 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 Telothyriiniare a phylogenetically nested sub-clade within the Dexiinae( Stireman et al. 2019); this evidence, is still the subject of discussion, as the reconstruction of the Dexiinaeis still unclear. So, for the sake of continuity, taking into account all the available evidence, and given the remarkable difference between  Telothyriaand other genera within the Dexiinae, the authors have chosen to maintain the Telothyriinias a monotypic tribe, until further examination is conducted to clarify its classification.