Hantu niah, Huber, 2016
publication ID |
https://doi.org/ 10.5852/ejt.2016.186 |
publication LSID |
lsid:zoobank.org:pub:B73C6A06-1245-41CB-9175-C33BC2273245 |
DOI |
https://doi.org/10.5281/zenodo.10812831 |
persistent identifier |
https://treatment.plazi.org/id/0C378095-994C-427A-8989-E119A644A7EC |
taxon LSID |
lsid:zoobank.org:act:0C378095-994C-427A-8989-E119A644A7EC |
treatment provided by |
Jeremy |
scientific name |
Hantu niah |
status |
gen. et sp. nov |
Hantu niah View in CoL gen. et sp. nov.
urn:lsid:zoobank.org:act:0C378095-994C-427A-8989-E119A644A7EC
Figs 3–6 View Figs 1 – 6 , 26–39 View Figs 26 – 30 View Figs 31 – 39 , 43–45 View Figs 40 – 45
Gen.n. Bor20 – Huber et al. 2015a: 73–74.
Diagnosis
Easily distinguished from H. kapit gen. et sp. nov. by absence of horns in male ocular area ( Fig. 31 View Figs 31 – 39 ), by highly distinctive male palp ( Figs 26–27 View Figs 26 – 30 ; square-shaped trochanter apophysis; dorsal process on procursus), by strong distal apophyses on male chelicerae ( Fig. 28 View Figs 26 – 30 ), and by scape on epigynum ( Figs 29 View Figs 26 – 30 , 43 View Figs 40 – 45 ) more sclerotized and without Fne transversal folds. From other putatively close relatives in the genera Khorata and Savarna by male procursus shape (dorsal process) and epigynal scape.
Etymology
The species name is derived from the type locality; noun in apposition.
Type material
MALAYSIA-BORNEO: holotype, Ƌ, Sarawak, Niah Cave N.P. , forest near cave, 3.814° N, 113.771° E, 40 m a.s.l., 28 Jul. 2014 (B.A. Huber), ZFMK ( Ar 15071 ) GoogleMaps .
Other material examined
MALAYSIA-BORNEO, Sarawak: 10 ƋƋ, 15 ♀♀, 1 juv., same data as holotype, ZFMK ( Ar 15072–73 ; 9 ƋƋ, 14 ♀♀) GoogleMaps and SMK (1 Ƌ, 1 ♀) GoogleMaps ; 4 ♀♀, same data, in pure ethanol, ZFMK ( Bor 226 ) GoogleMaps ; 2 ♀♀, Niah Cave N.P. , forest along main trail, 3.814– 3.821° N, 113.763– 113.771° E, 20–40 m a.s.l., 27 Jul. 2014 (B.A. Huber, S.B. Huber), ZFMK ( Ar 15074 ) GoogleMaps ; 1 ♀, 1 juv., same data, in pure ethanol, ZFMK ( Bor 177 ) GoogleMaps .
Description
Male (holotype)
MEASUREMENTS. Total body length 2.3, carapace width 1.0. Leg 1: 20.5 (5.0 + 0.4 + 5.1 + 7.7 + 2.3), tibia 2: 3.0, tibia 3: 2.2, tibia 4: 2.9; tibia 1 L/d: 58. Distance PME-PME 420 µm, diameter PME 90 µm, distance PME-ALE 25 µm, no AME.
COLOR. Carapace light ochre with narrow lateral dark margins and large median dark mark including ocular area. Clypeus not darkened. Sternum dark brown. Legs ochre to light brown, without dark rings. Abdomen grey with large dorsal and lateral marks; ventrally with three large dark marks (in genital area, at spinnerets, and in-between).
BODY. Habitus as in Figs 3–4 View Figs 1 – 6 ; ocular area slightly raised, each triad on short stalk directed toward lateral ( Fig. 31 View Figs 31 – 39 ); carapace with shallow but distinct thoracic furrow; clypeus unmodiFed; sternum wider than long (0.65/0.55), unmodiFed. Chelicerae as in Fig. 28 View Figs 26 – 30 , with pair of proximal lateral apophyses and pair of strong distal apophyses curved toward median line; without modiFed hairs.
PALPS. As in Figs 26–27 View Figs 26 – 30 , coxa with sclerotized protruding rim ventro-distally; trochanter with short but very large, square-shaped ventral apophysis with very small teeth distally; femur very large, without processes; patella unusually long; tibia long and slender. Procursus very long; with distinctive dorsal process and complex tip. Bulb oval, with simple weakly sclerotized embolus.
LEGS. With single ventral row of ~10 spines on femora 1; without curved hairs; with short vertical hairs in two dorsal rows on all femora and tibiae; retrolateral trichobothrium on tibia 1 at 7.5%; prolateral trichobothrium absent on tibia 1, present on other tibiae. Tarsus 1 pseudosegments indistinct, only distally ~20 visible in dissecting microscope.
Male (variation)
Tibia 1 in 8 other males: 4.8–5.3 (mean 5.0). Margins of carapace sometimes not dark; dorsal pattern on abdomen sometimes indistinct. Number and thickness of spines on femora variable, from few barely thicker hairs (small males) to ~20 distinct spines (large males).
Female
In general similar to male ( Figs 5–6 View Figs 1 – 6 ); eye triads closer together (distance PME-PME 220 µm), not on stalks ( Fig. 34 View Figs 31 – 39 ); no spines on femora; fewer vertical hairs on femora and tibiae (but especially on tibiae also with higher than usual density). Tibia 1 in 16 females: 4.3–4.7 (mean 4.5). Entire epigynal area protruding, posteriorly sclerotized with distinctive scape ( Figs 29 View Figs 26 – 30 , 43, 44 View Figs 40 – 45 ); internal genitalia as in Figs 30 View Figs 26 – 30 and 45 View Figs 40 – 45 .
Natural history
The spiders were found close to the ground in small domed webs among and under rocks, under dead leaves, and in little cavities. They were extremely efFcient at escaping through the closed hand, then dropped to the ground and remained motionless, becoming essentially invisible.
Distribution
Known from Niah Cave N.P. only ( Fig. 7 View Fig. 7 ).
Discussion
Pholcid spiders are widely known for their long-legged representatives, some of which are synanthropic, but a large number of species in a range of genera are actually relatively short-legged ground and litterdwellers. About half of all currently recognized genera either include or consist entirely of such shortlegged species (e.g., Huber 2005a, 2005b, 2011, 2013, 2015; Huber et al. 2005). This suggests multiple convergent shifts among microhabitats; in fact, molecular data support the notion that such shifts have occurred repeatedly in various directions ( Huber et al. 2010; Dimitrov et al. 2013; see also Huber & Dimitrov 2014).
Ground and litter-dwelling pholcids share a similar habitus to a degree that allows reasonable predictions even for museum specimens without microhabitat information. They are small (body size ~ 1–3 mm), relatively short legged (leg 1 length <30 mm), rather dark (brown), and have a globular or oval abdomen. This combination seems to be extremely rare in pholcids living in other microhabitats. The only apparent exception known to me are West and Central African representatives of the genus Anansus Huber, 2007 that were collected by canopy fogging ( Huber 2007).
In Southeast Asia, at least seven pholcid genera other than Hantu gen. nov. include ground and litterdwelling representatives: Aetana Huber, 2005 ; Belisana Thorell, 1898 ; Holocneminus Berland, 1942 ; Pholcus Walckenaer, 1805 ; Savarna Huber, 2005 ; Spermophora Hentz, 1841 ; and wugigarra Huber, 2001.
ZFMK |
Germany, Bonn, Zoologische Forschungsinstitut und Museum "Alexander Koenig" |
SMK |
SMK |
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