Two new Cypridopsinae ostracods, Potamocypris meissnerisp. nov. and Sarscypridopsis harundinetisp. nov. are described. Both were found only as asexual (all-female) populations in temporary waters of southern Africa. Potamocypris meissneri was collected from a small pan in the North-West Province of South Africa. It is approximately 0.5 mm long and belongs to the species group with long swimming setae on the second antennae. However, the species has a somewhat isolated position in the genus owing to the conspicuously reticulated carapace, which is furthermore densely covered by prominent conuli with normal pores carrying long sensilla, as well as to the wide anterior and posterior flanges on the left valve. To allow identification of the new species in relation to its closest congeners, a key to the species of the genus Potamocypris Brady, 1870 from southern Africa is provided. The genus Sarscypridopsis McKenzie, 1977 mostly has an Afrotropical distribution with only few species occurring in other regions. Sarscypridopsis harundineti was collected from floodplains of the outskirts of the Okavango Delta in Botswana. It is approximately 0.4 mm long and can be distinguished from congeners mainly by the smaller and more oval-shaped valves. We conclude that southern African Cypridopsinae urgently need integrated taxonomic revision, by means of both morphological characters and DNA-sequence data.

Botswana constitutes a major gap in our knowledge of the distribution of Ostracoda in the region of Southern Africa, restraining thorough biogeographic interpretations. We combine records from previously published surveys along with our own field collections to provide a collation of living and fossil (Late Pleistocene to Holocene) Ostracoda recorded in Botswana. Our survey yielded 17 species, of which nine species have not been recorded before in the country. Including the present update, 54 species (45 living and nine fossil or subfossil) belonging to 22 genera of five families (with 76% species belonging to the family Cyprididae) are currently reported from Botswana. Yet, 23 taxa are left in open nomenclature, indicating the urgent need for sound systematic studies on harmonizing taxonomy of Southern African ostracods, especially of those inhabiting small temporary waterbodies, considered as threatened with extinction before being properly described or discovered. This updated checklist provides detailed information about the distribution and habitat of each recorded species. Species richness, distribution patterns, and diversity of ostracod species regionally and in different freshwater ecoregions are also discussed. We found low alpha (site) diversity (mean 3.3 species per site) and a significant difference in species composition and beta diversity of the Okavango ecoregion versus the Kalahari and Zambezian Lowveld ecoregions.

Our knowledge of the ecology of non-marine Ostracoda inhabiting endorheic wetlands (pans) of the semi-arid regions of South Africa is very scarce. The present study investigates the distribution of ostracod species in grass, open, and salt pans in the central part of the North West province and tests ostracod response to abiotic and biotic predictor variables operating at a local scale. Distance-based linear models revealed three variables (pan type, water electrical conductivity and abundance of macroinvertebrate predators, and collector-gatherers) that best explained variation in the ostracod dataset. Ostracod assemblages from the three studied pan types differed by the dominance structure rather than by the species composition. Salt pans with high conductivity and high ratio of predaceous macroinvertebrates were dominated by Heterocypris giesbrechti, with accessory presence of Plesiocypridopsis newtoni. In open pans with low conductivities and the lowest ratio of predators (but highest ratio of collector-gatherers) Potamocypris mastigophora was typically a dominant species, while in grass pans, all the three mentioned species had similar relative abundances. Although our findings lend provisional support to some models of ostracod assemblage diversity across different pan types, more studies replicating endorheic depression wetlands in other regions are required before generalizations can be made.

No abstract

No abstract