9 research outputs found

    From Naples 1963 to Rome 2013 — A brief review of how the International Research Group on Ostracoda (IRGO) developed as a social communication system.

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    The 1st International Symposiumon Ostracoda (ISO) was held in Naples (1963). The philosophy behind this symposiumand the logical outcome of what is nowknown as the International Research Group on Ostracoda (IRGO) are here reviewed, namely ostracodology over the last 50 years is sociologically analysed. Three different and important historic moments for the scientific achievements of this domain are recognised. The first one, between about 1963 and 1983, is related to applied research for the oil industry aswell as to the great interest in the better description of the marine environment by both zoologists and palaeontologists. Another important aspect during this period was thework by researchers dealing with Palaeozoic ostracods,who had their own discussion group, IRGPO. Gradually, the merger of this latter group with those dealing with post-Palaeozoic ostracods at various meetings improved the communication between the two groups of specialists. A second period was approximately delineated between 1983 and 2003. During this time-slice, more emphasis was addressed to environmental research with topics such as the study of global events and long-term climate change. Ostracodologists profited also from the research “politics” within national and international programmes. Large international research teams emerged using new research methods. During the third period (2003–2013), communication and collaborative research reached a global dimension. Amongst the topics of research we cite the reconstruction of palaeoclimate using transfer functions, the building of large datasets of ostracod distributions for regional and intercontinental studies, and the implementation of actions that should lead to taxonomic harmonisation. Projects within which molecular biological techniques are routinely used, combined with sophisticated morphological information, expanded now in their importance. The documentation of the ostracod description improved through new techniques to visualise morphological details, which stimulated also communication between ostracodologists. Efforts of making available ostracod information through newsletters and electronic media are evoked

    Quantitative relationship between water-depth and sub-fossil ostracod assemblages in Lake Donggi Cona, Qinghai Province, China

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    A calibration data set of 51 surface sediment samples from Lake Donggi Cona on the northeastern Tibetan Plateau was investigated to study the relationship between sub-fossil ostracod assemblages and water depth. Samples were collected over a depth range from 0.6 to 80 m. A total of 16 ostracod species was identified from the lake with about half of the species restricted to the Tibetan Plateau and its adjacent mountain ranges and poorly known in terms of ecological preferences, and the other half displaying a mainly Holarctic distribution. Living macrophytes and macroalgae were recorded in Lake Donggi Cona down to a depth of about 30 m, and bivalve (Pisidium cf. zugmayeri) and gastropod (Gyraulus, Radix) shells were found down to depths of 43 and 48 m, respectively. The ostracod-waterdepth relationship was assessed by multivariate statistical analysis and ostracod-based transfer functions for water depth were constructed. Weighted averaging partial least squares (WA-PLS) regression provided the best model with a coefficient of determination r2 of 0.91 between measured and ostracod-inferred water depth, a root mean square error of prediction of 8% and a maximum bias of 10.6% of the gradient length, as assessed by leaveone-out cross-validation. Our results show the potential of ostracods as palaeo-depth indicators in appropriate settings. However, transfer-function applications using fossil ostracod assemblages for palaeo-depth estimations require a thorough understanding of the palaeolimnological conditions of lakes and therefore detailed multi-proxy analysis to avoid misinterpretation of ostracod-based inferences

    Sediment penetration depths of epi- and infaunal ostracods from Lake Geneva (Switzerland)

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    Many (palaeo-)environmental parameters can be deduced from ecological and chemical analyses of ostracods. However, the specific ecology of each taxon has a great impact on its reaction to changing environmental conditions. As a consequence, each taxon records these changes differently. The mean penetration depth (MPD) and relative individual abundances have been documented along sediment depth profiles for the dominant sub-littoral to profundal species of ostracods in western Lake Geneva, Switzerland, and this data can be used to estimate their preferential habitat in terms of sediment depths. Isocypris beauchampi, Limnocytherina sanctipatricii, Cypria ophtalmica forma lacustris at 13-m water depths, Limnocythere inopinata, and a winter generation of Herpetocypris reptans have the shallowest habitat preferences at the study sites (MPDs of 0.45, 0.48, 0.49, 0.60, and 0.81 cm, respectively). These results suggest that these populations may be regarded as being preferentially epifaunal forms. Populations of Cytherissa lacustris (MPDs of 0.61, 0.73, and 0.82 cm at 13-, 33-, and 70-m water depths, respectively), Cypria ophtalmica forma lacustris at 70 m (MPD = 0.96 cm), Fabaeformiscandona caudata (MPD = 0.99 cm), and a summer generation of Herpetocypris reptans (MPD = 1.03 cm) were identified as being infaunal. Candona neglecta is the species that was found the deepest in the sediment of Lake Geneva, with MPDs of 0.65, 1.22, and 1.30 cm at 13-, 33-, and 70-m water depths, respectively. Information on the sediment texture and oxygen concentrations inferred from the analyses of sediment pore water suggest that the oxygen content of the sediment pore water is not the only dominant parameter controlling the differences in ostracod sediment penetration depths observed among the different sites, but that they might also be influenced by the sediment 'softness,' which itself depends on grain size, water content, and the abundance of organic matter in sediment
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