Clubiona filicata
publication ID |
https://doi.org/ 10.5281/zenodo.181670 |
DOI |
https://doi.org/10.5281/zenodo.6228344 |
persistent identifier |
https://treatment.plazi.org/id/692187BD-FFC3-FFD3-FF0D-FE71404B7729 |
treatment provided by |
Plazi |
scientific name |
Clubiona filicata |
status |
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Clubiona filicata View in CoL O. P.- Cambridge, 1874
( Figs 5–7 View FIGURES 5 – 10 , 30–33 View FIGURES 30 – 33 )
Clubiona filicata View in CoL O. P.- Cambridge, 1874: 413, fig. 35 (description of ɗ, Ψ); Gravely 1931: 261, fig. 16d; Tikader & Biswas 1981: 69, figs 120–121; Gong 1989: 109, figs 1–13; Majumder & Tikader 1991: 23, figs 30–35; Bis-
was & Raychaudhuri 1996: 199, figs 27–33; Song, Zhu & Chen 1999: 415, figs 245L–M, 248F–G. Clubiona swatowensis Strand, 1907: 562 View in CoL (Description of Ψ); Strand 1909: 39, fig. 24.
Material examined. THAILAND: Chaiyaphum Province and District: 2ɗ, Thad Tone National Park, 15.– 20.xi.2006, leg. P. Dankittipakul ( MHNG, TNHM).
Diagnosis. Males of C. filicata can be easily recognized by the following features: an apical appendage of the male palp consists of a truncate embolus with a triangular retrolateral tubercle and a very long, filiform conductor that gives impression of the embolus ( Figs 6–7 View FIGURES 5 – 10 , 30–32 View FIGURES 30 – 33 ); a digitiform tegular apophysis ( Fig. 31 View FIGURES 30 – 33 ) located anterio-prolaterally on the tegulum, situated close to the base of an apical appendage. Clubiona filicata closely resembles another species in the japonica -group, C. biembolata , in possessing a filiform conductor and enlarged posterior median eyes (see also Deeleman-Reinhold 2001: figs 67, 69). The latter species differs in the lack of a dorsal pattern on the opisthosoma (replaced by a lightly sclerotized dorsal scutum occupying ¾ of opisthosoma length) as well as the absence of a tegular apophysis on the male palp. The female can be recognized by its epigynal atrium situated anteriorly, by parallel insemination ducts running longitudinally to the posterior spermathecae and by the more or less triangular spermathecal heads.
Description. Male (Thad Tone National Park): Total length 4.2; prosoma 2.0 long, 1.4 wide; opisthosoma 2.2 long, 1.2 wide.
Coloration and pattern ( Fig. 5 View FIGURES 5 – 10 ). Prosoma longly oval, narrowed in pars cephalica; in profile slightly higher behind longitudinal fovea; integument smooth, clothed with short fine hairs. Dorsal shield of prosoma pale yellow, slightly darker in front, without distinctive color pattern; fovea reddish. Chelicerae dark brown. Labium and endites yellowish brown. Sternum pale yellow. Legs pale yellow; anterior tibiae, metatarsi and tarsi distinctly darker. Opisthosoma elongate-oval; dorsum with a pattern consisting of dark purple blotches and stripes; venter pale. Spinnerets white.
Male palp ( Figs 6–7 View FIGURES 5 – 10 , 30–33 View FIGURES 30 – 33 ). Retrolateral tibial apophysis broad at base, gradually tapering towards its tip. Cymbium excavated dorso-apically, a profound depression covered with thick patch of short hairs. Bulb oval; sperm duct sinuate, forming a double loop. Tegular apophysis digitiform, situated proapically. Apical appendage consisting of truncate embolus and very long filiform conductor, forming a coiled structure, directed distad.
Natural history. The specimen examined was obtained from a Malaise trap set in a deciduous forest. The collecting locality, Thad Tone National Park, locates on Phu Lan Ka mountain range and consists of dipterocarp forest and lowland evergreen forest.
Distribution. South and Southeast Asia: India, Bangladesh, Pakistan, China and Thailand (new record, Fig. 69 View FIGURE 69 ); probably common in tropical forests of Indochina.
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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Clubiona filicata
Dankittipakul, Pakawin & Singtripop, Tippawan 2008 |
Clubiona filicata
Majumder 1991: 23 |
Gong 1989: 109 |
Tikader 1981: 69 |
Gravely 1931: 261 |
Cambridge 1874: 413 |