48 resultados para trombose venosa

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Magellania venosa, the largest recent brachiopod, occurs in clusters and banks in population densities of up to 416 ind/m**2 in Comau Fjord, Northern Chilean fjord region. Below 15 m, it co-occurs with the mytilid Aulacomya atra and it dominates the benthic community below 20 m. To determine the question of why M. venosa is a successful competitor, the in situ growth rate of the brachiopod was studied and its overall growth performance compared with that of other brachiopods and mussels. The growth in length was measured between February 2011 and March 2012 after mechanical tagging and calcein staining. Settlement and juvenile growth were determined from recruitment tiles installed in 2009 and from subsequent photocensus. Growth of M. venosa is best described by the general von Bertalanffy growth function, with a maximum shell length (Linf) of 71.53 mm and a Brody growth constant (K) of 0.336/year. The overall growth performance (OGP index = 5.1) is the highest recorded for a rynchonelliform brachiopod and in the range of that for Mytilus chilensis (4.8-5.27), but lower than that of A. atra (5.74). The maximal individual production (PInd) is 0.29 g AFDM/ind/year at 42 mm shell length and annual production ranges from 1.28 to 89.25 g AFDM/year/m**2 (1-57% of that of A. atra in the respective fjords). The high shell growth rate of M. venosa, together with its high overall growth performance may explain the locally high population density of this brachiopod in Comau Fjord. However, the production per biomass of the population (P/B-ratio) is low (0.535) and M. venosa may play only a minor role in the food chain. Settling dynamics indicates that M. venosa is a pioneer species with low juvenile mortality. The coexistence of the brachiopod and bivalve suggests that brachiopod survival is affected by neither the presence of potential brachiopod predators nor that of space competitors (i.e. mytilids).

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Succession was already studied over decades. The present thesis investigated the succession on hard substrate at two different study sites within the fjord Comau, Chile. Nine plates were installed at both sites (mouth of fjord and inner fjord) and photographed over three years. Additionally the natural community was recorded and a ground truthing was carried out to verify the analyzed species. Respectively at both sites over 50 different species were identified. Abundance data decreased with only one exception continuously, whereas the percentage cover increased. But the communities on the recruitment plates do still not reach the community structure of the natural environment. The present data showed that the hard-bottom succession in the fjord Comau is best described by the TOLERANCE MODEL (Connell & Slatyer, 1977). An important species of the natural community is the stony coral Desmophyllum dianthus, which normally (outside the fjord) grows beneath 1000 m water depth. The results of this work indicate that the mature community is not reached after 36 months.

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The Marion Plateau is a large carbonate platform off northeastern Queensland. Three sites (815, 816, and 826) were drilled on this platform and form the basis for this study. Larger benthic foraminifers, together with rare planktonic forms from the shallow-water carbonates that form the main part of the platform sequence, were studied to establish a biostratigraphy. The presence of Lepidocyclina (Nephrolepidiná) howchini sensu lato and Ladoronia vermicularis, together with Globorotalia (Globorotalia) praemenardii and Orbulina, indicate an early middle Miocene (N9-N12) age (i.e., lower Tf stage) for these carbonates. Dolomitization has destroyed much of the original fabric of these carbonates, making study of the larger foraminifers difficult. Sites 815 (forereef location) and 826 (backreef, lagoonal setting) provide the best faunas. However, at all sites nodular coralline algae and Halimeda are the major bioclasts; coral fragments form a major component at Sites 816 and 826. The middle Miocene neritic sequence is separated from the overlying hemipelagic sequence by an unconformity that spans much of the middle and late Miocene. At Site 815, which is in a forereef situation, the overlying hemipelagic sequence contains a Zone N17A fauna, but at Site 816, higher on the platform, a similar sequence contains a Zone N19 fauna. The faunas indicate that the platform was built up during the early middle Miocene and remained at fairly constant water depths and temperatures during this period. It was then exposed prior to subsiding rapidly during the late Miocene and Pliocene to depths similar to those of the present day.