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Ostracods belonging to the genus Bennelongia differ much in valve morphology between adults and juveniles. Adult valves are asymmetrical, characterised by a beak-like feature in the anteroventral region of the left valve, and, with some notable exceptions, mostly have smooth or weaklyornamented valves. Juvenile specimens, on the other hand, have valves that are almost symmetrical, with no beak-like feature and are often heavily ornamented. We have examined the last 3 - 4 juvenile stages of 6 Bennelongia species from 5 different lineages, in order to decipher the types of external valve ornamentation and their recurrences during ontogeny and across lineages. It is clear that ornamentation is more prevalent at the early instar stages compared to the last 2 pre-adult stages, and especially when compared to the adult stage itself. We also examined the surprising presence of a calcified inner lamella with a prominent inner list in the pre-adult stages of Bennelongia species, that is usually absent in juveniles of other ostracods, thus questioning if heterochronic processes have provided an intermediate valve morphology between the simple (normal) cypridinid juvenile state and the heavily derived and modifi ed state of adult Bennelongia. We discuss the possible (speculative) functionality of the ornamentation in juveniles.
The ostracod genus Bennelongia De Deckker & McKenzie, 1981 is endemic to Australia and New Zealand. Extensive sampling in Western Australia (WA) revealed a high specific and largely undescribed diversity. Here, we describe seven new species belonging to the B. barangaroo lineage: B. timmsi sp. nov., B. gnamma sp. nov., B. hirsuta sp. nov., B. ivanae sp. nov., B. mcraeae sp. nov., B. scanloni sp. nov. and B. calei sp. nov., and confirm the presence of an additional species, B. dedeckkeri, in WA. For five of these eight species, we could construct molecular phylogenies and parsimonious networks based on COI sequences. We also tested for cryptic diversity and specific status of clusters with a statistical method based on the evolutionary genetic species concept, namely Birky’s 4 theta rule. The analyses support the existence of these five species and a further three cryptic species in the WA B. barangaroo lineage. The molecular evidence was particularly relevant because most species described herein have very similar morphologies and can be distinguished from each other only by the shape, size and position of the antero-ventral lapel on the right valve, and, in sexual populations, by the small differences in shape of the hemipenes and the prehensile palps in males. Four species of the WA B. barangaroo lineage occur in small temporary rock pools (gnammas) on rocky outcrops. The other four species are mainly found in soft bottomed seasonal water bodies. One of the latter species, B. scanloni sp. nov., occurs in both claypans and deeper rock pools (pit gnammas). All species, except for B. dedeckkeri, originally described from Queensland, have quite clearly delimited distributions in WA. With the seven new species described here, the genus Bennelongia now comprises 25 nominal species but several more await formal description.