Arsipoda povilaensis, Samuelson & Biondi, 2016
publication ID |
https://doi.org/ 10.5852/ejt.2016.230 |
publication LSID |
lsid:zoobank.org:pub:80B8573D-AEF3-4E98-A9C8-BF652ED4124E |
DOI |
https://doi.org/10.5281/zenodo.3853561 |
persistent identifier |
https://treatment.plazi.org/id/6E5BDE56-5D9F-4E95-AC92-7CA05D7CAD8E |
taxon LSID |
lsid:zoobank.org:act:6E5BDE56-5D9F-4E95-AC92-7CA05D7CAD8E |
treatment provided by |
Valdenar |
scientific name |
Arsipoda povilaensis |
status |
sp. nov. |
Arsipoda povilaensis sp. nov.
urn:lsid:zoobank.org:act:6E5BDE56-5D9F-4E95-AC92-7CA05D7
Figs 2D View Fig , 5A View Fig , 9E View Fig , 11L View Fig , 15B View Fig
Diagnosis
Arsipoda povilaensis sp. nov. shares a thickset, ovoid body with A. atra sp. nov., A. evax and A. transversa sp. nov. ( Figs 1B, F View Fig , 2D, I View Fig ). It can be distinguished by the yellowish integuments ( A. evax is black and metallic, A. atra sp. nov. is black, and A. transversa sp. nov. is reddish); compared to A. transversa sp. nov., with which it can be more easily confused, it also displays a less transverse and less convex pronotum ( Fig. 5A, D View Fig ). Genitalia are also clearly distinguishable ( Figs 8C, G View Fig , 9E View Fig , 10A View Fig , 11B, F, L, P View Fig ).
Etymology
The specific name is a Latinized adjective formed after Povila, the type locality where the species has been collected.
Type material
Holotype
NEW CALEDONIA (N): ³, Pic d’Amoa (Povila), -20.95020 165.29320, 400–450 m, rainforest, 17 Nov. 2010, R. Ruta and M. Wanat leg. ( MNHN). GoogleMaps
Paratypes
NEW CALEDONIA: 1 ³, 3 ♀♀, same data of the holotype ( MNHW); 1 ³, Pic d’Amoa (Povila), -20.9510 165.29120, 400 m, lower rainforest, 18 Nov. 2010, M. Wanat and R. Ruta leg. ( MNHW); 3 ♀♀, ditto, end 0.5 km of road, -20.95530 165.29100, 450 m, 18 Nov. 2010 ( MNHW); 1 ♀, ditto, -20.95659 165.29103, 23 Nov. 2010, M. Wanat leg. ( MNHW); 1 ♀, Pic d’Amoa, 20°57.2' S 165°17.5' E, 360 m, forest, at light, 14 Jan. 2007, R. Dobosz and M. Wanat leg. ( USMB).
Description of the holotype (³)
Body thickset, slightly convex ( Fig. 2D View Fig ); LB = 2.38 mm; maximum pronotal width at base (WP = 0.85 mm); maximum elytral width at basal third (WE = 1.18 mm). Dorsum yellowish, not metallic. Frons and vertex microreticulate and punctate; head grooves weakly impressed, not continued to postantennal region; genae and frontal carina short; antennae slightly longer than ½ body length ( LAN = 1.28 mm; LAN/LB= 0.54), basally yellow, gradually and slightly darker towards apex; LA:100:6 7:56:56:78:78:78:78:89:78:122. Pronotum trapezoidal, clearly transverse (LP = 0.51 mm; WP/LP = 1.66), laterally weakly convex ( Fig. 5A View Fig ); anterior angles distinctly prominent; antebasal transverse sulcus weakly impressed, slightly sinuate, without clearly distinguishable lateral fovea; pronotal surface microreticulate, with small and dense punctuation, similar to that on head. Elytra slightly elongate (LE = 1.73 mm; WE/ LE = 0.68), laterally clearly arcuate; punctuation quite small, but distinctly larger than on pronotum; interstriae very finely microreticulate and micropunctuate. Legs yellow; first pro- and mesotarsomeres distinctly dilated; adhesive setae present on ventral side of first pro-, meso- and, partially, metatarsomeres. Venter light brown; last abdominal ventrite laterally clearly incised, without special preapical impressions. Median lobe of aedeagus (LAED = 0.94 mm; LE/LAED = 1.83) ( Fig. 9E View Fig ) in ventral view laterally parallel, slightly narrower in pre-apical part; apex rounded; in lateral view median lobe curved at basal third, then straight; apex sinuate, ventrally oriented; dorsal ligula from half length to apical part of median lobe of aedeagus, narrow.
Biometry
Male (n = 3; range): 1.60 Ĺ LE Ĺ 1.73 mm; 1.05 Ĺ WE Ĺ 1.08 mm; 0.48 Ĺ LP Ĺ 0.51 mm; 0.81 Ĺ WP Ĺ 0.85 mm; 1.25 Ĺ LAN Ĺ 1.28 mm; 0.94 Ĺ LAED Ĺ 0.94 mm; 2.16 Ĺ LB Ĺ 2.38 mm; 3.37 Ĺ LE/LP Ĺ 3.42; 1.26 Ĺ WE/WP Ĺ 1.38; 1.66 Ĺ WP/LP Ĺ 1.79; 0.66 Ĺ WE/LE Ĺ 0.68; 0.54 Ĺ LAN/LB Ĺ 0.59; 1.69 Ĺ LE/ LAED Ĺ 1.83.
Female (n = 8; mean and standard deviation; range): LE = 1.68 ± 0.04 mm (1.63 Ĺ LE Ĺ 1.74 mm); WE = 1.10 ± 0.04 mm (1.03 Ĺ WE Ĺ 1.15 mm); LP = 0.48 ± 0.01 mm (0.48 Ĺ LP Ĺ 0.51 mm); WP = 0.83 ± 0.03 mm (0.80 Ĺ WP Ĺ 0.88 mm); LAN = 1.13 ± 0.04 mm (1.10 Ĺ LAN Ĺ 1.18 mm); LSPc = 0.17 ± 0.01 mm (0.16 Ĺ LSPc Ĺ 0.18 mm); LB = 2.24 ± 0.08 mm (2.16 Ĺ LB Ĺ 2.34 mm); LE/LP = 3.46 ± 0.10 (3.27 Ĺ LE/LP Ĺ 3.58); WE/WP = 1.32 ± 0.04 (1.29 Ĺ WE/WP Ĺ 1.39); WP/LP = 1.72 ± 0.04 (1.66 Ĺ WP/ LP Ĺ 1.76); WE/LE = 0.66 ± 0.02 (0.62 Ĺ WE/LE Ĺ 0.68); LAN/LB = 0.51 ± 0.01 (0.49 Ĺ LAN/LB Ĺ 0.52); LE/LSPc = 10.06 ± 0.46 (9.38 Ĺ LE/LSPc Ĺ 10.86).
Paratypes very similar in shape and sculpture to the holotype. Some specimens slightly darker on elytra. Spermatheca ( Fig. 11L View Fig ) with rounded basal part; collum length about twice as long as apical part; ductus thickset, elongate, apically inserted.
Distribution
Endemic to the Pic d’Amoa, Central Grande Terre ( Fig. 15B View Fig ).
Ecological notes
Collected in rainforest between 360 and 450 m a.s.l. No information about host plants is available.
MNHN |
Museum National d'Histoire Naturelle |
LAN |
Lancing College |
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.
Kingdom |
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Phylum |
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Class |
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Order |
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SubOrder |
Polyphaga |
SuperFamily |
Chrysomeloidea |
Family |
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SubFamily |
Galerucinae |
Tribe |
Alticini |
Genus |