Micropholcus fauroti

Huber, Bernhard A., 2009, Four new generic and 14 new specific synonymies in Pholcidae, and transfer of Pholcoides Roewer to Filistatidae (Araneae), Zootaxa 1970, pp. 64-68: 66

publication ID

zt01970p068

persistent identifier

http://treatment.plazi.org/id/8D7DE08A-371D-1F74-ACE9-5D9CAF08E7AE

treatment provided by

Donat

scientific name

Micropholcus fauroti
status

 

Micropholcus fauroti  (Simon, 1887)

Mariguitaia divergentis  González-Sponga, 2004: 64-67; pl. 1, figs. 1-9; new synonymy.

Mariguitaia museorum  González-Sponga, 2004: 68-70; pl. 2, figs. 1-9; new synonymy.

Mariguitaia neoespartana  González-Sponga, 2004: 70-72; pl. 3, figs. 1-9; new synonymy.

Mariguitaia sucrensis  González-Sponga, 2004: 72-75; pl. 4, figs. 1-7; new synonymy.

Justification of synonymies. Two lines of evidence strongly support the synonymies: the characters used by González- (2004) to diagnose the species, and the microhabitats of the “new” species. Biogeographic data support the conclusions .

Characters. As for Tibiosa  above, most of González-Sponga’s (2004) drawings of the palps are good enough to immediately hint at M. fauroti  (drawings in Millot 1941, 1946, Deeleman-Reinhold & Prinsen 1987, Saaristo 2001, Beatty et al. 2008). The retrolateral views all show the characteristic dorsal hinged process of the procursus. No comparable structure exists in any other known pholcid. More difficult to interpret are the prolateral views, especially the bulbal projections. In M. fauroti  , the bulb bears several very complex projections that are partly sclerotized and partly transparent . This, together with the small size (about 0.2 mm) makes these projections difficult to understand. Nevertheless, the drawings all show the principal lines seen in M. fauroti  .

Among the drawings of the male chelicerae, only the one in plate 3 comes very close to the actual situation in M. fauroti  , with one pair of distal and two pairs of proximal projections. In all other drawings, the lateral proximal pair is missing. These proximal apophyses are difficult to see unless the chelicerae are detached from the specimen. The drawing in plate 1 suggests that González-Sponga did not detach the chelicerae: it shows the chelicerae together with the palpal endites, erroneously fused into a single structure.

The epigynum of M. fauroti  is an externally simple oval plate with a transparent knob on its posterior border. The most distinctive feature is a median crescent-shaped internal structure visible through the cuticle. This is shown in all epigynal drawings in González-Sponga (2004). Lateral structures of similar shape but variable size (as in plates 2 and 3) are more or less visible in most M. fauroti  females.

All species diagnoses in González-Sponga (2004) include measurements, but in which sense these are supposed to be diagnostic is not stated. All measures are clearly within the range of M. fauroti  (e.g. tibia 1 length: 22 males from around the world: 5.0-7.0 mm, 39 females: 4.4-5.6; unpublished data). The four males and three females measured by González-Sponga (2004) are in fact surprisingly similar (e.g. tibia 1 length, males: 5.7-6.2 mm, females: 4.8-5.1). As for carapace shape and eye positions, see Tibiosa  above.

Finally, one surprising character emphasized by González-Sponga (2004) is the single trichobothrium on the male palpal tibia in all " new species ". All M. fauroti  specimens (in fact all pholcids) I have ever seen have two trichobothria on the palpal tibiae. Since both trichobothria are equally easy (or difficult) to see, I have no explanation for this. A single trichobothrium was described by the same author for Anomalaia  (now Metagonia  ) mariguitarensis  ( González-Sponga 1998); subsequent study has shown that it also has two trichobothria (Huber 2000).

Microhabitat. In the introduction, González-Sponga (2004) writes that Mariguitaia  occurs "both in forests and in human dwellings" (my translation). However, three species were found in buildings only, the fourth under shrubs in the village of Mariguitar  . No specimen was collected in a forest.

Biogeography. The original distribution of Micropholcus  is difficult to reconstruct. Only one congener  of the type species is known: Micropholcus jacominae Deeleman & van Harten  , 2001 from Yemen. Micropholcus fauroti  is widely distributed around the world (Deeleman & Prinsen 1987, Saaristo 2001). I have seen M. fauroti  from many countries, including Venezuela ( Península de Paraguaná: Coro), Cuba, the Dominican Republic, and the USA (unpublished). A further record for Venezuela (Zulia: Maracaibo) was recently published by Colmenares-García (2008). The fewer records for this species than for C. lyoni  and P. globosus  may partly be due to the small size and pale colour of this species.