Protohermes dichrous (Brauer)
publication ID |
https://doi.org/ 10.11646/zootaxa.3620.4.1 |
publication LSID |
lsid:zoobank.org:pub:3234B0FB-5630-4080-A98B-2474C4A86C6D |
DOI |
https://doi.org/10.5281/zenodo.6149970 |
persistent identifier |
https://treatment.plazi.org/id/717887AC-CB05-FFAF-FF57-F9A3FBACD82E |
treatment provided by |
Plazi |
scientific name |
Protohermes dichrous (Brauer) |
status |
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Protohermes dichrous (Brauer) View in CoL
( Figs. 3 View FIGURES 1 – 3 , 20–26 View FIGURES 20 – 26 )
Neuromus dichrous Brauer, 1878: 205 . Type locality: Borneo.
Diagnosis. In appearance there are one pair of black markings on posterolateral portions of vertex and two pairs of black markings on pronotum, and the forewing has a darkened transverse band, which extends posteriorly to CuA vein, between proximal and median pale markings. Genitalia of this species are characterized by the male ninth sternum with a pair of broadly subtriangular posterior lobes and the male ectoproct, which widely connects with ninth tergum by a suboval base.
Description. Male. Body length 20–25 mm; forewing length 28–33 mm, hindwing length 26–30 mm.
Head ( Fig. 3 View FIGURES 1 – 3 ) yellow, vertex posterolaterally with a pair of subquadrate black markings; post-ocular spine almost absent. Compound eyes brown; ocelli yellow, medially margined black, lateral ocelli close to median ocellus. Antenna black with scape and pedicle yellow. Mouthparts yellow; mandible with distal half black; maxillary and labial palpi respectively with distal two segments brown.
Thorax ( Fig. 3 View FIGURES 1 – 3 ) yellow; pronotum with two pairs of black markings near lateral margins. Thoracic pilosity yellowish, much longer on meso- and metathorax. Legs yellow, with short dense yellowish setae; tarsal claws pale reddish brown. Wings hyaline, with several yellowish markings. Forewing slightly brownish; proximally with one subtriangular marking, medially with several irregular markings usually fused with each other, and with one round marking at distal 1/3; membrane between basal and median markings darkened into a short transverse band, posteriorly narrowed and extending to CuA. Hindwing almost hyaline with marginal area pale brown. Veins mostly yellowish; veins in costal area and dark area of forewing blackish brown; veins in distal area of hindwing pale brown. Rs 8 to 9-branched; MA bifurcate; 6–9 crossveins between R and Rs; anterior branch of MP 4 to 6–branched, posterior branch of MP 2-branched.
Abdomen yellow. Ninth tergum ( Fig. 21 View FIGURES 20 – 26 ) subtrapezoidal, with arcuately incised anterior margin and truncate posterior margin. Ninth sternum ( Fig. 22 View FIGURES 20 – 26 ) medially short, subtrapezoidal; posterior margin shallowly incised trapezoidal, forming a pair of subtriangular posterior lobes. Ninth gonostylus ( Fig. 22 View FIGURES 20 – 26 ) slender unguiform, directed posteriad in lateral view, with tip distinctly incurved. Ectoproct ( Fig. 21–23 View FIGURES 20 – 26 ) slender band-like, extremely elongate, ~5.0 times as long as ninth tergum, arcuately incurved with apex slightly narrowed and more or less bended ventrad; base widely connected to ninth tergum and slightly inflated into a suboval structure. Tenth gonocoxite ( Fig. 24 View FIGURES 20 – 26 ) arched, dorsomedially strongly expanded into a broad plate; lateral lobes digitiform, straightly directed posteriad.
Female. Body length 19–30 mm; forewing length 29–35 mm, hindwing length 27–32 mm.
Eighth gonocoxite ( Figs. 25–26 View FIGURES 20 – 26 ) in lateral view subtriangular with arcuately convex posterior margin, in ventral view posterior margin medially with a deep V-shaped incision. Ninth gonocoxite ( Fig. 25 View FIGURES 20 – 26 ) broad, posteriorly rounded and ventrally incised, with a small gonostylus. Ectoproct ( Fig. 25 View FIGURES 20 – 26 ) short, with posterior margin medially incised, leaving subtriangular dorsal and slightly shorter and thinner ventral lobes in lateral view.
Type material. Neotype 3, “ MALAYSIA: Sabah, Kimanis Road [5°26ʹN, 116°05ʹE], 4.IV.1998 ” (HFIC).
Additional materials. 13, Borneo (ISNB); 1Ƥ, Borneo, 1969 (NSMT); INDONESIA: 13, Java, Tosari [7°52ʹN, 112°54ʹE] (BMNH); 1Ƥ, Midden O-Borneo [= central eastern Borneo, collecting site in East Kalimantan], 16.X.1925, H.C. Siebers (RMNH); MALAYSIA: 1m, Nord[= North]-Borneo, Waterstradt (MZPW); Sabah: 132Ƥ, near Poring hotspring [6°02ʹN, 116°42ʹE], F. Hayashi (one male emerged from larva in 6.X.1994, two females emerged from larvae in 26.VI.1994, HFIC); 2Ƥ, Mt. Trus Madi, IV.1992, H. Karube (HFIC); 1Ƥ, Trus Madi, 1000 m, IV.2005, M. Sawai (HFIC); 13, Trus Madi, 1000m, 1–15.IV.2006, M. Sawai (HFIC); 3Ƥ, Trus Madi, 1000 m, 15/ 25.IV.2007, M. Sawai (HFIC); 3Ƥ, Trus Madi, 1000 m, 6/ 20.IV.2008, M. Sawai (HFIC); 1Ƥ, Kinabalu, Staudinger (SDEI); 132Ƥ, Kinabalu (ZMHU); 13, Gunong Monkobo, 5.48N, 116.56E, 974 m, 7–13.VIII.1987, K.R. Tuck (BMNH); 231Ƥ (paralectotypes of P. bellulus ), Mt. Kinabalu, Kiau [6°01ʹN, 116°29ʹE], 3000 ft [= 914 m], 4/ 10.IV.1929 (BMNH); 131Ƥ, Kinabalu Nat[ional]. P[ark]., H.Q. 5100 ft [= 1554 m], 14/ 19.II.1980, L. Oosterweghel (RMNH); 13, Kinabalu (RMNH); 23, 18 km on r[oa]d. Keningau-Kimanis, 5.26N, 116.05E, 1050 m, 20.XI.1987, J. Huisman & R. de Jong (RMNH); 2Ƥ, Long Pa Sia, Airtrip along S[outhern] Pa Sia, 4°25’N, 115°43’E, 1090 m, 14.X.1986, J. Huisman et al (RMNH); 13, Marak Parak [6°19ʹN, 116°44ʹE], at lights, beside primary forest, 25/ 26.V.1985, Schimdt, Schimdt & Starr (USNM); 132Ƥ, 10 mi [les] N[orth]W[est] of Keningau, 900 m, 9/ 11.X.1980, S. Nagai (EUMJ); 531Ƥ, Daerh Penapang, Crocker Range National Park, Kipandi Butterfly Park [5°59ʹN, 116°04ʹE], 700 m, 23/ 25.III.2011, O. Tominaga (HFIC); Labuan: 13 [5°18ʹN, 115°13ʹE] (RMNH).
Distribution. Indonesia (East Kalimantan); Malaysia (Labuan, Sabah).
Remarks. van der Weele (1906) noted that he did not find the Brauer’s types (two males) which should have been deposited in the NHMW. We also searched for these types in the NHMW recently, but failed to find them. Therefore, the primary types of this species are probably lost. Based on the original description by Brauer (1878), it is difficult to determine the exact identity of P. dichrous because there are three additional species ( P. bellulus , P. decolor , and P. goodgeri sp. nov.) that are closely related to and similar to P. d i c h ro u s. However, the only available redescription and illustration of the male genitalia of P. d i c h ro u s in van der Weele (1906) show that the specimen he described belongs to a different species from P. bellulus , P. decolor , and P. goodgeri sp. nov. We examined a numerous old specimens with van der Weele’s handwritten identification labels as P. dichrous and found that all the males and most females he examined belonged to only one species, which is different from P. bellulus , P. decolor , and P. goodgeri sp. nov., but a few female specimens belong to P. d e co lo r. In order to prevent unnecessary taxonomic change, we follow van der Weele’s concept of the male of P. d i c h ro u s and designate a Neotype from Sabah.
The male of P. dichrous differs from P. bellulus , P. dichrous , and P. goodgeri sp. nov. by the ninth sternum with a pair of broadly subtriangular posterior lobes and the ectoproct proximally connected to the ninth tergum by an suboval inflated base.
We have examined a large number of specimens of Corydalidae from Indonesia and Malaysia but found only one specimen of P. dichrous with a collecting site in Java. This specimen was probably collected during or before the 1900’s as it was also examined by van der Weele (1906). Old specimens with incorrect locality labels can be found occasionally in several European collections. These specimens were sold by native collectors and usually were incompletely or incorrectly labeled. Here we consider that the record of P. dichrous in Java is doubtful since no additional specimens nor records of Protohermes species are known from the island.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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