Pala
publication ID |
https://doi.org/ 10.11646/zootaxa.2944.1.1 |
persistent identifier |
https://treatment.plazi.org/id/03B087E5-5B15-FFE3-FF79-F361FB3DFA29 |
treatment provided by |
Felipe |
scientific name |
Pala |
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Pala group
Ten species are included in the Pala group: H. pala , H. maculopala , H. nanopala , H. palamita , H. formosopala , H. tritropis , H. torosopala , H. koje , H. dudgeoni , and H. fasciolata ( Figs. 202 View FIGURE 202 , 203 View FIGURE 203 , 206 View FIGURE 206 , 207 View FIGURE 207 , 210 View FIGURE 210 , 211 View FIGURE 211 , 214 View FIGURE 214 , 215 View FIGURE 215 , 218 View FIGURE 218 , 219 View FIGURE 219 ). Members of this group are very small to moderately sized (ca. 1.23 to 1.58 mm), with distinctive coloration, and a broad body shape. Species in this group (except H. tritropis ) are unique in the shape of the prosternal intercoxal process: it is relatively wide, the midlongitudinal carina is restricted to the anterior part of the prosternum, and the intercoxal part is wide and concave (e.g., Figs. 214 View FIGURE 214 , 219 View FIGURE 219 ). The color varies somewhat, but the pronotum usually does not have a fascia or macula, is usually light brown or testaceous, lighter than the frons and the elytra. In a few species the elytra are fasciate.
Some of the broadest species of PNG Hydraena are found in this group. The mesoventral intercoxal process (P2) is comparatively wide and concave, and all of the species have widely separated, carinate plaques. The protibiae of males are modified, but not markedly so. The male genitalia have a similar basic plan, with a tendency for the left paramere to be rotated toward the dorsal surface of the aedeagus (e.g. Figs. 220, 221 View FIGURES 220–221 ).
Members of the Pala group are similar to members of the Impala group, but the latter have the midlongitudinal carina of the prosternum extending the entire length; therefore the posterior part is not concave. Although H. tritropis lacks the concave prosternal intercoxal area, the carina is straight, not bisinuate as in members of the Impala group; the form of the aedeagus of this species also supports its placement in the Pala group. The female tergite X, gonocoxite, and spermatheca of H. pala are illustrated ( Fig. 411 View FIGURES 408–411 ); as expected, they show some similarities (setal patterns, spermatheca shape) with those structures in the Impala group, but have a very differently shaped tergite X ( Figs. 410, 411 View FIGURES 408–411 ).
Members of the Pala group have only been collected in lowland rain forest, at an elevation range of 160–400 m (maps Figs. 428 View FIGURES 427–428 , 527–533 View FIGURES 527–530 View FIGURES 531–534 ). Only the three following microhabitat descriptors are given in the locality records: "ex. gravel banks"; "unshaded creek, small to medium cobbles, gravel and fine sand (the latter in areas of slack water), filamentous algae on stony substrates, small accumulations of leaf litter"; "river."
Five species in the Pala group were collected from Kojé Creek in Area 3. In fact, four species in the group are only known from that site ( Fig. 528 View FIGURES 527–530 ). These collections were made during a large rotenone study ( Dudgeon 1990, 1994). A total of 13 species of Hydraena were collected, and the site is the type locality of seven species, six of which are only known from there. Probably because of the collection method, via rotenone, the specimens were not well preserved and most of them lack some or all of the legs, or parts of legs, and maxillary palpi. The species in the Pala group from Koje are quite difficult, and require dissection of males for reliable determinations. Because of this decomposed condition, many females (ca. 300) from the Koje site were not identified.
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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