Horniella kaengkrachan Yin and Li

Yin, Zi-Wei & Li, Li-Zhen, 2014, Revision of the Oriental genus Horniella Raffray (Coleoptera, Staphylinidae, Pselaphinae), Zootaxa 3850 (1), pp. 1-83 : 50-51

publication ID

https://doi.org/ 10.11646/zootaxa.3850.1.1

publication LSID

lsid:zoobank.org:pub:BFD1F483-4255-429B-9E17-8D4A9E559C5F

DOI

https://doi.org/10.5281/zenodo.6142765

persistent identifier

https://treatment.plazi.org/id/CD490758-D821-FFD9-FF01-459140CFFAD7

treatment provided by

Plazi

scientific name

Horniella kaengkrachan Yin and Li
status

sp. nov.

16. Horniella kaengkrachan Yin and Li , new species

Figs 27 View FIGURE 27 B, 29, 49B; Map 4 View MAP 4

Type material (7 ♂♂, 12 ♀♀). Holotype, ♂, labeled ‘ THAILAND: Phetchaburi, Kaeng Krachan Nat. Pk , 300–400 m, 17.xi.1985, Burckhardt- Löbl / Holotype [red], ♂, Horniella kaengkrachan sp. n., det. Yin & Li, 2014, MHNG’ . Paratypes: 2 ♀♀, same data as the holotype ; 3 ♂♂, 8 ♀♀, same data, except ‘ 450 m, 18.xi.1985 ’; 3 ♂♂, 2 ♀♀, same data, except ‘ 19.xi.1985 ’. All paratypes are housed in MHNG, and each bears a yellow type label similar to that of the holotype except ‘ PARATYPE ♂ (or ♀)’.

Description. Male ( Fig. 27 View FIGURE 27 B). Length 2.96–3.21 mm. Head about as long as wide, HL 0.64–0.67 mm, HW 0.64– 0.61 mm; anterolateral genal projections ( Fig. 29 View FIGURE 29 C) distinct, anterior margins roundly concave; median sulcus between antennal tubercles short; scapes ( Fig. 29 View FIGURE 29 B) angularly expanded at anterolateral margins; clubs ( Fig. 29 View FIGURE 29 A) loosely formed by apical three moderately enlarged antennomeres; venter with pair of short, relatively thick lateral spines ( Fig. 29 View FIGURE 29 D). Maxillary palpomeres II stout, widest near middle. Each eye composed of about 35–45 facets. Pronotum as long as wide, PL 0.59–0.64 mm, PW 0.58–0.61 mm. Elytra wider than long, EL 0.79–0.84 mm, EW 1.19–1.29 mm; shallow discal striae reaching apical 3/4 of elytral length. Protrochanters and profemora ( Fig. 29 View FIGURE 29 E) each with one long ventral spine, protibiae ( Fig. 29 View FIGURE 29 F) with small triangular spur; mesotrochanters ( Fig. 29 View FIGURE 29 G) with extremely short, apically blunt ventral spine, mesofemora and mesotibiae ( Fig. 29 View FIGURE 29 H) simple; tarsomeres II normal, not extending to beneath tarsomeres III. Abdomen large, AL 0.94–1.06 mm, AW 1.22–1.23 mm, tergite IV (first visible tergite) with distinct median carina extending to apical 3/4 of tergal length, lacking lateral discal carinae, tergite V lacking median carina. Sternite IX ( Fig. 29 View FIGURE 29 I) with well-sclerotized apical half, and membranous narrowed basal half. AeL 0.61 mm; aedeagus ( Figs 29 View FIGURE 29 J–L) with nearly symmetric median lobe, apex obliquely truncate; endophallus complicated, composed of four major sclerites.

Female. Similar to male in general appearance; each eye composed of about 25 facets; profemora each with two ventral spines near base, lacking spine or spur on mid and hind legs. BL 2.79–3.01 mm, HL 0.62–0.65 mm, HW 0.53–0.58 mm, PL 0.56–0.61 mm, PW 0.56–0.59 mm, EL 0.73–0.74 mm, EW 1.06–1.16 mm, AL 0.87–1.02 mm, AW 1.19–1.22 mm. Genital complex ( Fig. 49 View FIGURE 49 B) weakly sclerotized, composed of broadly transverse, platelike apical sclerite, and elongate membranous basal portion.

Differential diagnosis. This species is placed as a member of the H. burckhardti group. As discussed above, males share with H. intricata the roundly concave anterior margins of the apicolateral genal projections, the short and apically blunt ventral spine on the mesotrochanters, the nearly symmetric aedeagal median lobe with an obliquely truncate apex, and complicated structure of the aedeagal endophallus. These two species are easily separated by the weakly-developed expansion on the lateral margins of the scapes, the presence of a triangular apical spur on the mesotibiae in H. kaengkrachan , which also has a completely different form of the aedeagal endophallus.

Distribution. Thailand: Phetchaburi ( Map 4 View MAP 4 ).

Collection notes. Adults were collected from leaf litter samples by sifting and use of Winkler-Moczarski extractors.

Etymology. The new species is named after its type locality, the Kaeng Krachan National Park.

MHNG

Museum d'Histoire Naturelle

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