Poupinia hirsuta Guinot, 1991
publication ID |
https://doi.org/ 10.5281/zenodo.5397969 |
persistent identifier |
https://treatment.plazi.org/id/C5482F17-9027-FFCE-C5CD-FABCFB5EFB8E |
treatment provided by |
Marcus |
scientific name |
Poupinia hirsuta Guinot, 1991 |
status |
|
Poupinia hirsuta Guinot, 1991 View in CoL
Female 54 × 41 mm, allotype, French Polynesia, Raiatea (MNHN-B 24346).
It was possible to observe partly the skeleton and the spermatheca of this female without immersion in a bath of potassium hydroxyde. Its carapace was partly detached from the rest of the body, and the spermatheca was visible only on one side. The thoracic sternum ( Fig. 20 View FIG ) is relatively wide, medially with a large, flat, and translucid horizontal area. All sutures are lateral, except for suture 6/7, which forms a transverse ridge throughout most of its course, but bends sharply backwards and slightly inwards at the level of the P3 coxae (Guinot 1991: pl. 3F). At each extremity of its horizontal course, suture 6/7 shows a marked spine in the male, while there is only a prominence in the female. Sternite 8 is longitudinally divided by a very short median line, and the sternoabdominal notch is deep. As in the Homolidae , the sternal plate bears large and well delimited sterno-coxal depressions at the level of the P2, P3 and P4 (sterno-coxal depressions 5, 6, 7).
Sternites 5, 6 and 7 of Poupinia hirsuta bear paired formations looking like setiferous cupules ( Figs 20 View FIG ; 21 View FIG ). Each cupule (small cup) comes in contact with the basal region of the corresponding coxa, specifically with its inflated supracondylar part, which shows a different texture and is covered by a very short, worn tomentum, mixed with longer setae along the margins. These cupules exist only in the female, while they are absent in the male, which shows similar P2-P4 coxae, with inflated and tomentose supra-condylar areas.
The axial skeleton of Poupinia is very peculiar, and such a disposition had never been described. There is a wide and short intertagmal phragma (i n c o n t r a s t t o l o n g i t u d i n a l l y e x t e n d e d i n Homola ranunculus , Fig. 18 View FIG ), but the center of the body is empty ( Fig. 22 View FIG ). This means that the short endopleurites and endosternites exclusively join laterally and do not present the median connections (by interfingering) seen in the other Homolidea. Poupinia lacks the median mass that constitutes the transverse binding between the two lateral endopleural parts, either by interfingering ( Homolodromiidae , Homolidae , Latreilliidae ) or by fusion ( Dromiidae , Dynomenidae, Cyclodorippoidea, Raninoidea , all Eubrachyura). Nevertheless, careful examination revealed that the external surface of the lateral endosternites were covered by irregular elongated structures, contrasting with the smooth surface of the intertagmal phragma ( Fig. 22B View FIG ). These structures actually correspond to the digitations (presumably corresponding to extremities of interosternites) that normally constitute the transverse, median binding by interfingering in the Homolidea. Here they are displaced to the sides so that Poupinia , as in the other Homolidea, actually presents interdigitations, but in a different location. We speculate that these digitations will ultim a t e l y f u s e w i t h e n d o p l e u r i t e s i n a n o t h e r evolutionary stage. The original condition of the Poupiniidae is now completed by this unusual skeletal organization. The skeletal data support the views pointed out by Guinot (1995) that Poupiniidae is unique to the Podotremata . However, if placement of the family Poupiniidae in the Homolidea remains unquestioned, this newly presented character does not permit to surely interpret it as a basal or advanced condition in this subsection. We will have to wait pending a more thorough investigation into the skeletal morphology and diversity in the Anomura, the Astacidea Latreille, 1802, and the Palinura Latreille, 1802. It is true that the relationships of the Archaeobrachyura (as a whole or partly) remain debatable.
Externally, the spermatheca occupies approximately the two-thirds of suture 7/8 and lies far from transversal suture 6/7. There is an extended aperture corresponding to the wole membranous area, which is relatively simple ( Fig. 20 View FIG ). Internally, the chamber is very inflated on its inner side and is filled by sperm.
CONCLUSIONS FOR THE HOMOLIDEA
In the Homolidea the sternum around the sutures 7/8 is modified to form the external part of the spermathecae, with distinct membranous areas belonging either to sternite 7, or to sternite 8, or to both. The relatively large spermathecal apertures are always situated on a level with female gonopores on the P3 coxae. The internal organization is rather similar among the genera and species, always with a chamber never far from the aperture and directly opening on the exterior.
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.