256 resultados para occurrence number


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Pack ice around Svalbard was sampled during the expedition ARK XIX/1 of RV "Polarstern" (March-April 2003) in order to determine environmental conditions, species composition and abundances of sea-ice algae and heterotrophic protists during late winter. As compared to other seasons, species diversity of algae (total 40 taxa) was not low, but abundances (5,000-448,000 cells/l) were lower by one to two orders of magnitude. Layers of high algal abundances were observed both at the bottom and in the ice interior. Inorganic nutrient concentrations (NO2, NO3, PO4, Si(OH)4) within the ice were mostly higher than during other seasons, and enriched compared to seawater by enrichment indices of 1.6-24.6 (corrected for losses through the desalination process). Thus, the survival of algae in Arctic pack ice was not limited by nutrients at the beginning of the productive season. Based on less-detailed physical data, light was considered as the most probable factor controlling the onset of the spring ice-algal bloom in the lower part of the ice, while low temperatures and salinities inhibit algal growth in the upper part of the ice at the end of the winter. Incorporation of ice algae probably took place during the entire freezing period. Possible overwintering strategies during the dark period, such as facultative heterotrophy, energy reserves, and resting spores are discussed.

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In the East Indian Ocean direct contribution of land volcanism to sedimentation appears as interlayers of tephra and tuffaceous sediments, pumice fragments, and dispersed volcanoclastic materials of silty grain size. Similarity of distribution of tephra, tuffaceous sediments, Ethmodiscus ooze, and turbidites in the Pleistocene section results from deposition of all these materials under controll of a single factor, namely synchronous redistribution owing to seismic activity on the ocean floor and on the Sunda Islands. Burial of layers of oxidized deposits and formation of iron-manganese nodules is at least partly related to global climate cooling and to circulation of ocean waters.

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Calcareous nannoplankton biostratigraphy has been worked out in the eastern Mediterranean utilizing deep-sea sediments recovered from DSDP Leg 42A Sites 375 and 376. These two drill sites were located approximately 55 km west of Cyprus on the Florence Rise. Sediments, ranging in age from early Miocene (Helicosphaera ampliaperta Zone) through Holocene, contain sufficient age-diagnostic species to recognize essentially all of the lowlatitude nannoplankton zones described by Bukry, although regional, secondary marker species are needed to define some zonal boundaries. Reworked Cretaceous and Paleogene nannoplankton occur throughout the stratigraphic interval studied, but not in quantities large enough to mask indigenous species. Sedimentation rates at Sites 375 and 376 were highest in the late Miocene and late Pleistocene. Open-marine, warm-water species of discoasters are present in significant numbers throughout the Miocene and Pliocene. Earliest Pliocene assemblages contain numerous specimens of ceratoliths. Nannoplankton in post-Messinian sediments at the drill sites and the Zanclean stratotype at Capo Rossello, Sicily, indicate that the base of the Amaurolithus tricorniculatus Zone (base of Triquetrorhabdulus rugosus Subzone) corresponds with the Miocene-Pliocene boundary.

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The common occurrence of parallel phenotypic patterns suggests that a strong relationship exists between ecological dynamics and micro-evolution. Comparative studies from a large number of populations under varying sets of ecological drivers could contribute to a better understanding of this relationship. We used data on morphology of arctic charr (Salvelinus alpinus) and ecological factors from 35 Icelandic lakes to test the hypothesis that morphological patterns among monomorphic charr populations from different lakes are related to interlake variation in ecological characteristics. There is extensive phenotypic diversity among populations of Icelandic charr, and populations are easily distinguished based on overall body morphology. The results obtained in the present study showed that the morphological diversity of charr was related to large-scale diversity in lake ecology. Variation in charr morphology was related to water origin (e.g. spring fed versus run-off), bedrock age, and fish community structure. The present study shows how various ecological factors can shape the biological diversity that we observe.