Dyscolus silvestris Moret, 2020
publication ID |
https://doi.org/ 10.5852/ejt.2020.646 |
publication LSID |
lsid:zoobank.org:pub:4C9F63B2-DB17-4EDB-ADEE-13AC9EFB921B |
DOI |
https://doi.org/10.5281/zenodo.3848391 |
persistent identifier |
https://treatment.plazi.org/id/8DA5B9B7-F332-4D75-AC2D-CEBBD34ADA3C |
taxon LSID |
lsid:zoobank.org:act:8DA5B9B7-F332-4D75-AC2D-CEBBD34ADA3C |
treatment provided by |
Valdenar |
scientific name |
Dyscolus silvestris Moret |
status |
sp. nov. |
Dyscolus silvestris Moret View in CoL sp. nov.
urn:lsid:zoobank.org:act:8DA5B9B7-F332-4D75-AC2D-CEBBD34ADA3C
Figs 52–53 View Figs 52–53
Etymology
Latin adjective meaning ‘forest related’.
Type material
Holotype
ECUADOR • ♂; Napo Province, Termas de Papallacta ; 3300 m a.s.l.; 1 Jul. 2001; P. Moret leg.; “sousbois”; QCAZ.
Paratypes (5 ♂♂, 10 ♀♀)
ECUADOR – Napo Province • 1 ♂, 1 ♀; same collection data as for holotype; CPM • 1 ♂, 1 ♀; Papallacta, Termas Jamanco, Waypoint 41 ; 0°22′24.6″ S, 78°10′5.5″ W; 3410 m a.s.l.; 25 Oct. 2015; P. Moret leg.; MNHN GoogleMaps • 1 ♀; same collection data as for preceding; QCAZ GoogleMaps • 1 ♂, 3 ♀♀; same collection data as for preceding; CPM GoogleMaps • 1 ♂; same collection data as for preceding; COI voucher PM041-02, BOLD sequence SUM103-18; CPM GoogleMaps • 1 ♀; same collection data as for preceding; COI voucher in ethanol PM041-06, BOLD sequence SUM104-18; CPM GoogleMaps • 2 ♀♀; Lago Papallacta ; 3370 m a.s.l.; 9 Apr. 1986; A. Vigna; CPM • 1 ♀; Papallacta ; 2700 m a.s.l.; 6–8 Apr. 1979; H. Frania leg.; UASM • 1 ♂; Lago Papallacta ; 0°20′29″ S, 78°10′23″ W; 3400 m a.s.l.; 6 Nov. 1999; R. Anderson leg.; CMNC GoogleMaps .
Diagnostic description
Habitus: Fig. 52 View Figs 52–53 . Wingless. Body length: 9.1–10.0 mm. Body colour variable, predominantly dark brown with reddish brown areas in some specimens; legs, antennae and mouthparts reddish brown. Elytral microsculpture isodiametric. Head broad and convex, neck slightly constricted, eyes moderately bulging. Pronotum subcordiform, the base much narrower than the apex; sides arcuate anterad, markedly sinuate posterad; hind angles obtuse, sharp; two pairs of lateral setae. Elytra subovate, moderately convex; striae entire, well impressed; intervals flat. Third elytral interval with 3–4 discal setae. Legs: protarsi of the male much broader than those of the female. Fifth metatarsomere asetose ventrally. Last visible abdominal ventrite with one pair (♂) or two pairs (♀) of setae along its apical margin. Male genitalia: Fig. 53 View Figs 52–53 . Median lobe arcuate, shortly and bluntly triangular at apex, endophallus unarmed. Female genitalia: unstudied.
Comparisons
Dyscolus silvestris Moret sp. nov. is similar to the shorter and broader individuals of Dyscolus denigratus . The main differences are: head slightly bigger and broader; sides of the pronotum sinuate basally, hind angles sharply obtuse (completely rounded in D. denigratus ); femora of the male not swollen as in D. denigratus . The apex of the median lobe of the male genitalia has a shorter apex, and the endophallus is entirely unarmed (with a heavily sclerotized area in D. denigratus ).
Habitat
Upper montane forest on the Amazonian slope of the Andes , from 2700 to 3400 m a.s.l. This species lives in the leaf litter.
Geographic distribution
Only known from the type locality around Papallacta in Northern Ecuador, probably microendemic.
QCAZ |
Ecuador, Quito, Pontificia Universidad Catolica del Ecuador, Catholic Zoology Museum |
MNHN |
France, Paris, Museum National d'Histoire Naturelle |
UASM |
Canada, Alberta, Edmonton, University of Alberta, E.H. Strickland Entomological Museum |
CMNC |
Canada, Ottawa, Canadian Museum of Nature |
QCAZ |
Museo de Zoologia, Pontificia Universidad Catolica del Ecuador |
CPM |
Christoffel Park Museum |
MNHN |
Museum National d'Histoire Naturelle |
UASM |
University of Alberta, E.H. Strickland Entomological Museum |
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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