Megarthrus wayqecha Pérez, Rodríguez & Asenjo, 2020
publication ID |
https://doi.org/ 10.11646/zootaxa.4731.4.11 |
publication LSID |
lsid:zoobank.org:pub:58EB7FD6-8724-4546-89BC-66187D340D16 |
DOI |
https://doi.org/10.5281/zenodo.3665119 |
persistent identifier |
https://treatment.plazi.org/id/D381BA9B-848E-4D9B-B125-37EE635F93D4 |
taxon LSID |
lsid:zoobank.org:act:D381BA9B-848E-4D9B-B125-37EE635F93D4 |
treatment provided by |
Plazi |
scientific name |
Megarthrus wayqecha Pérez, Rodríguez & Asenjo |
status |
sp. nov. |
Megarthrus wayqecha Pérez, Rodríguez & Asenjo View in CoL , sp. nov.
( Figs. 1–21 View FIGURES 1–7 View FIGURES 8–16 View FIGURES 17–19 View FIGURES 20–21 )
urn:lsid:zoobank.org:act:D381BA9B-848E-4D9B-B125-37EE635F93D4
Type material (43♂♂, 51♀♀). Holotype: PERU : ♂, labeled “PERU: CU[Department of Cuzco], Kosñipata, / Wayqecha , Trocha / Canopy , 13°11’32.8’’S, / 71°35’16.0’’W, 2931 m,” “ 02.xi.2017, cloud forest, / sifting of leaf litter, M. / Rodríguez & L. Pérez leg.” “ HOLOTYPE [red label] / Megarthrus wayqecha / sp. nov. / Desig. Pérez et al., 2019” ( MUSM) GoogleMaps . Paratypes (94): 32♂♂, 33♀♀ labeled with the same data as holotype (21♂♂, 28♀♀ MUSM; 2♂♂, 1♀ MEKRB; 1♂, 1♀ CEMT; 2♂♂, 1♀ FMNH; 2♂♂, 1♀ MHNG; 1♂, 1♀ VMDC; 2♂♂, MPEG; 1 ♂, IADIZA) GoogleMaps . 3 ♂♂ labeled as holotype with additional green label “DNA BARCODING / VOUCHER / BOLD Sys- tems / CCDB-30362-B01 to B03” ( MUSM) . 2♂♂, 6♀♀ labeled “PERU: CU[Department of Cuzco], Kosñipata, / Wayqecha Research / Center , 13°10’29.07’’S,” “ 71°35’11.98’’W, 2950 m, / 23.x.2017, cloud forest, /sifting of leaf litter, M. / Rodríguez & L. Pérez leg.” ( MUSM) GoogleMaps . “ Peru: Cuzco Dept. /, Pillahuata. Manu rd, / km 126, 24.IX.1982, / FMND #82-2861, ex” “vine litter & fungus / nr. seepage area, / L. E. Watrous and G. / Mazurek ”(2 ♀♀ FMNH) ; same data but “km 128, 17.IX.1982, FMND #82-249, ex litter & seepage area” (1 ♀ FMNH) ; same data but “ 19. IX.1982, FMND #82-262, ex litter nr. falls” (1 ♂, 1♀ FMNH) ; same data but “ 23.IX.1982, FMND #82-281, ex litter & fungus nr. seepage area” (2 ♀♀ FMNH) ; same data but “ 25.IX.1982, FMND #82-293, ex litter, some nr. stream” (1♂, 2 ♀♀ FMNH; 2 ♂♂ MHNG) ; same data but “ 26.IX.1982, FMND #82-299, ex litter along stream” (1 ♂, 2 ♀♀ FMNH, 2 ♀♀ MHNG) ; same data but “ 27.IX.1982, FMND #82-307, ex leaf litter”(1 ♂ FMNH) . All paratypes labeled “ PARATYPE [yellow label] / Megarthrus wayqecha / sp. nov. / Desig. Pérez et al., 2019” .
Diagnosis. Among the members of the genus possessing the eleventh antennomeres piriform, Megarthrus wayqecha sp. nov. uniquely shares with the Argentinian M. ogloblini Bruch, 1940 (Fig. 147: Cuccodoro 2011) and the Colombian M. andinus López-García et al., 2011 the pronotum shallowly notched laterobasally with the lateral outline forming 4 distinct angles. However M. andinus is readily distinguished from these species by its conspicuous anterior adsutural elytral humps, and M. ogloblini has the male metatibiae cylindrical bearing peg-like setae on apical half, while males of M. wayqecha have the metatibiae enlarged and notched with peg-like setae grouped subapically. The shape of the aedeagus of M. wayqecha is also diagnostic: the median lobe in lateral view has the ventral face subapically straight with the tip of apex acute ( Fig. 18 View FIGURES 17–19 ) and the dorsal valve (seen in dorsal view) is Vshaped ( Fig. 19 View FIGURES 17–19 ).
Description. Holotype male (BL=3.11, BW=1.18, PL+EL=1.82). Body dark brown with appendages and legs somewhat paler, antennomeres 9–11 paler than antennomeres 1–8 ( Fig. 1 View FIGURES 1–7 ). Dorsal pubescence of body fairly uniform, frontal setae directed forward, median area of frons less dense than on vertex; pronotum, elytra and abdomen with setae directed backward, denser on pronotum than on elytra, pronotal setae curved and recumbent, denser on pronotal disc; elytral setae curved and recumbent, becoming denser near humeral area with interspaces as wide as puncture diameters; metaventral pubescence uniform, with small protuberance near posterior margin; pubescence on abdominal tergites parallel, uniform. Frons with granulation conspicuous, with granulae about as high as their diameter or higher; pronotum and elytra granulofossulate, with granulation small.
Head ( Fig. 3 View FIGURES 1–7 ) wider than long (HW=0.71, HL=0.53), mesal portion of disc strongly convex in lateral view; Ushaped frontal impression shallow; eyes medium size on posterior half; clypeus carinate, nearly rounded; temples convex in dorsal view. Antenna ( Fig. 2 View FIGURES 1–7 ) symmetrical and filiform, 2.1 times longer than pronotum, antennomeres 1–4 without pubescence, antennomeres 5–11 pubescent; antennomere 11 piriform.
Pronotum wider than long (PW=1.27, PL=0.65), 1.2 times longer than head, anterior margin slightly concave and posterior margin slightly convex and bilobed in the middle ( Fig. 4 View FIGURES 1–7 ). Pronotum with disc strongly convex and deeply depressed near middle of lateral edges, lateral and posterior edges shallowly depressed along disc. Anterior angles projected forward, lateral contours forming four denticles, posterior angles weakly projected backwards. Medial groove punctate and flat, slightly narrower in middle ( Fig. 4 View FIGURES 1–7 ). Hypomeron with inner edge wider in its median portion, ridged from anterior margin to laterobasal angle, without a discal pit. Proventral medial ridge absent.
Scutellum triangular with anterior border rounded and posterior border slightly acute, margins slightly raised and with pubescence directed backward. Elytra wider than long (EL=0.96, EW=1.30), 1.8 times longer than pronotum, gradually widened toward apex ( Fig. 2 View FIGURES 1–7 ), humeral callus raised, moderately convex; disc with low swellings, moderately depressed posteriorly and along lateral external edge, the latter finely carinate, slightly arcuate in dorsal view. Protrochanter without transverse ridge, small, subtriangular with one macroseta near the apex; profemur oblong with base flattened; protibia thin and shorter than profemur, inner face with many setae in the apical two thirds; protarsomere 1–4 dorsoventrally setose, protarsomere 1 as long as protarsomere 2–3 combined, protarsomere 5 with scarce setae, longer than protarsomere 1. Mesotrochanter subtriangular with peg-like setae arranged in two rows, one row with 7–8 peg-like setae and the second with 4–5 peg-like setae, and bearing one subapical macroseta ( Fig. 5 View FIGURES 1–7 ); mesofemur oblong; mesotibia sinuate, shorter than mesofemur, with peg-like setae arranged in two rows, a row along 4/5 apical length and a short row from base to middle, and some apical peg-like setae not aligned ( Fig. 6 View FIGURES 1–7 ); mesotarsomeres similar to protarsomeres. Metatrochanter subtriangular, incrassate ( Fig. 7 View FIGURES 1–7 ); metafemur strongly very robust about twice as long as broad (0.71/0.30) ( Fig. 7 View FIGURES 1–7 ); metatibia gradually enlarged toward apex, shorter than metafemur, with notched at subapical quarter constriction, and with peg-like setae grouped on apical quarter ( Fig. 7 View FIGURES 1–7 ); metatarsomeres similar to protarsomeres.
Tergites III–VII pubescent with one pair of paratergites; tergites II–III covered by elytra, tergite IV partially covered. Medial process of sternite II shorter and smaller than medial process of sternite III ( Fig. 11 View FIGURES 8–16 ). Sternite III– VII rectangular with pubescence. Tergite VIII triangular with anterior angles slightly projected forward, posterior margin forming an obtuse angle ( Fig. 8 View FIGURES 8–16 ), with small and broad medial apical projection convex in lateral view ( Fig. 9 View FIGURES 8–16 ). Sternite VIII trapezoidal, with lateral margin slightly convex, posterior margin strongly concave and membranous with four short macrosetae, anterior margin characteristic, inner plate asymmetrical with apex acute exceeding a little the anterior margin of sternite VIII ( Fig. 10 View FIGURES 8–16 ). Hemitergites IX slightly asymmetrical, left hemitergite slightly bigger in ventral view, anterior margin of right hemitergite more concave than left ( Fig. 12 View FIGURES 8–16 ). Sternite IX asymmetrical, oblong and thin ( Fig. 12 View FIGURES 8–16 ).
Aedeagus as in Figs. 13–14 View FIGURES 8–16 (internal sac evaginated), with median lobe oval-shaped in ventral view ( Fig. 13 View FIGURES 8–16 ), in lateral view with ventral face subapically straight with the tip of apex acute ( Fig. 14 View FIGURES 8–16 ), dorsal valve V-shaped.
Female. Similar to male, except mesotrochanter without peg-like setae; mesotibia without peg-like; metafemur thin; metatibia without peg-like setae; tergite VIII in lateral view with little and thin medioapical projection convex; sternite VIII without inner plate and posterior margin almost straight; genital segments as in Figs. 15–16 View FIGURES 8–16 ; gonocoxal plate lacking mediodorsal ridge.
Remarks. The new species M. wayqecha sp. nov. is included in the definition of Megarthrus inaequalis - supergroup proposed by Cuccodoro (2011a) based on the following characters: presence of a long prohypomeral ridge extended posteriorly to the laterobasal angle, frontal pubescence directed forward ( Figs. 1, 3 View FIGURES 1–7 ), antennomere 11 piriform ( Figs. 1, 2 View FIGURES 1–7 ), and lack of adventral adhesive setae on the first male protarsomere. Within this supergroup only M. wayqecha , M. andinus and the Costa Rican M. mammiger Bierig, 1940 , lack a mediodorsal ridge on the female gonocoxal plate. However, M. mammiger has the pronotum conspicuously notched laterobasally, while it is only slightly notched laterobasally in M. wayqecha and M. andinus . Megarthrus wayqecha differs notably from M. andinus by its elytra lacking conspicuous antebasal adsutural humps. The sexually dimorphic features on the male legs, the shape of the aedeagal ventral wall, and the conformation of the female valvifers are also diagnostic.
Aedeagus with the internal sac not evaginated from a paratype as in Figs. 17–19 View FIGURES 17–19 .
Three male paratypes and 16 female paratypes have the antennomere 9 yellow in apical half and brown in basal half.
Distribution and natural history. The specimens fron wayquecha were collected in a cloud forest between 2931 m and 2950 m, from the biological station “Wayqecha”, a private area recently protected by Peruvian law with the aim to preserve the biodiversity of Peruvian Yungas (MINAM, 2016) ( Figs. 20, 21 View FIGURES 20–21 ). Wayqecha is placed 19 km SW of Pillahuata (13°08’S, 71°25’W), the type locality of M. machu Cuccodoro, 2001 . According to the information provided by the collector, the specimens were found in leaf litter with moss, ferns, and bamboo leaves alongside the roots and trunks of trees as observed in Fig. 21 View FIGURES 20–21 .
Etymology. The specific name “Wayqecha” refers to the locality of collection of this new species. Wayqecha means ‘little brother’ in Quechua language. This is a noun in apposition.
Barcoding. The mitochondrial DNA sequences (COI) of three paratypes were identical ( Table 1 View TABLE 1 ). One COI sequence is as follows:
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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