Calapnita dinagat, Bernhard A. Huber, 2017
publication ID |
https://doi.org/ 10.5281/zenodo.273086 |
publication LSID |
lsid:zoobank.org:pub:0FA0F51A-3868-4F13-A93D-E34CA5A689F8 |
DOI |
https://doi.org/10.5281/zenodo.6040249 |
persistent identifier |
https://treatment.plazi.org/id/03B66F68-8502-0700-FF6A-FE7A2F79F884 |
treatment provided by |
Plazi |
scientific name |
Calapnita dinagat |
status |
sp. nov. |
Calapnita dinagat View in CoL sp. nov. Figs 131 View FIGURES 128 – 133 , 236–244 View FIGURES 236 – 253
Diagnosis. Distinguished from other species of vermiformis group by shape of procursus (bifid ventral flap and distinctive prolateral process, Figs 236–238 View FIGURES 236 – 253 ) and by additional ventral process close to distal ventral process on male palpal femur (arrow in Fig. 240 View FIGURES 236 – 253 ). From most species also by small pedipalps ( Figs 287–288 View FIGURES 285 – 288 ). From C. bario and C. bariengi also by distal cheliceral apophyses clearly bipartite ( Fig. 241 View FIGURES 236 – 253 ); from several species also by dark male sternum and by oval pore plates in transversal orientation ( Fig. 244 View FIGURES 236 – 253 ).
Etymology. The species name is derived from the type locality; noun in apposition.
Material examined. Holotype. PHILIPPINES: ♂, ZFMK (Ar 16052), Dinagat Island , near Libjo , Paragua Forest , ‘site 1’ (10.222°N, 125.553°E), 130 m a.s.l., forest at brook, on leaf, 20.ii.2014 (B.A. Huber, P.N. Banaag). GoogleMaps
Other material. PHILIPPINES: 2♂ 5♀ 2 juvs, ZFMK (Ar 16053), same data as holotype GoogleMaps ; 2 juvs in absolute ethanol, ZFMK (Phi 233), same data GoogleMaps .
Description. Male (holotype)
MEASUREMENTS. Total body length 5.5, carapace width 0.75. Leg 1: 31.5 (8.0 + 0.3 + 7.1 + 13.6 + 2.5), tibia 2: 5.5, tibia 3: 3.4, tibia 4: 6.1; tibia 1 L/d: 118. Distance PME-PME 200 µm, diameter PME 90 µm, distance PME- ALE ~30 µm; no trace of AME.
COLOR. Entire animal mostly pale gray to whitish, sternum darker, legs slightly yellowish with brown patellae and tibia-metatarsus joints.
BODY. Habitus as in Fig. 131 View FIGURES 128 – 133 ; ocular area barely elevated, each triad on very low hump; carapace without median furrow; clypeus unmodified; sternum as wide as long (0.48), unmodified.
CHELICERAE. As in Figs 241–242 View FIGURES 236 – 253 , with pair of bipartite apophyses near lamellae, pair of lateral processes; without modified hairs; without stridulatory ridges.
PALPS. In general similar to C. vermiformis (cf. figs 139 and 140 in Huber 2011) but much smaller; trochanter apophysis as in Fig. 239 View FIGURES 236 – 253 ; femur as in Fig. 240 View FIGURES 236 – 253 , distal process at 24% of femur length; tibia length/diameter 0.43/ 0.27; procursus as in Figs 236–238 View FIGURES 236 – 253 , with conical semitransparent prolateral process, with flat bifid ventro-distal sclerite; bulb length 0.29; embolus length 0.35.
LEGS. Without spines and curved hairs; few vertical hairs; retrolateral trichobothrium on tibia 1 at 2%; prolateral trichobothrium absent on tibia 1, present on other tibiae; tarsus 1 pseudosegments not seen in dissecting microscope.
Male (variation). Tibiae 1 missing in other males.
Female. In general similar to male but sternum whitish; eye triads slightly closer together (distance PME-PME 190 µm). Tibia 1 in 4 females: 5.2, 5.2, 5.6, 5.7. Epigynum as in Fig. 243 View FIGURES 236 – 253 , weakly sclerotized with wide anterior ‘knob’; internal genitalia as in Fig. 244 View FIGURES 236 – 253 , with oval pore plates far apart.
Natural history. One male had an ectoparasitic mite on its prosoma ( Fig. 131 View FIGURES 128 – 133 ; cf. C. bankirai above). Such mites are not rare in spiders (e.g., Welbourn & Young 1988) but have rarely been reported for Pholcidae .
Distribution. Known from type locality on Dinagat Island only ( Fig. 284 View FIGURE 284 ).
ZFMK |
Zoologisches Forschungsmuseum Alexander Koenig |
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.