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Spatial size variations of labial palps, gills and the adductor muscle of the invasive feral oyster, Crassostrea gigas, were studied along two gradients of suspended particulate matter (SPM) concentrations in the temperate macrotidal Bourgneuf Bay, (annual mean SPM concentration gradient of 21.0–154.0 mg l−1) and the adjacent Loire Estuary (annual mean SPM concentration gradient of 24.1–630.4 mg l−1) on the French Atlantic Coast. The gill-to-palp (G:P) ratios decreased with increasing turbidity, both in the bay and the estuary. Changes in G:P ratios were chiefly related to palp area variations, increasing gradually from low turbidity to very high-turbidity sites, while gill area showed no clear relationship with turbidity conditions. The G:P ratio, showing a significant relationship (r2 = 0.97) with SPM concentrations, is proposed as a pallial organ index of oyster acclimation to turbidity conditions. The area of the striated part of the adductor muscle was always greater than that of the smooth one, and adductor muscle area tended to decrease when SPM concentration increased. These observations show the morphological capacity of the oyster C. gigas to tolerate SPM concentrations above the feeding cessation thresholds previously determined experimentally. They also suggest that pallial organ size variations could help explain the success of recent feral oyster invasions in temperate turbid ecosystems.  相似文献   
2.
Yves  Gruet 《Marine Ecology》1986,7(4):303-319
Abstract. Important intertidal sabellarian reefs are built by the polychaete Sabellaria alveolata (LINNÉ) in the Mont Saint-Michel Bay in Normandy at Champeaux (France). Typical profiles and plans were done over a ten year period. At the same time, population dynamics were examined during the last six years. At this site a nearly complete morphological cycle spread itself over more than ten years. Initially built on rock substrate (primary settlement phase), the studied reefs actually lie on a sandy shore. The growth phase begins by stages of balls which are then joined with new settlements between or on older tubes (secondary settlement). This phase comes to an end with an important platform stage. Then, the destruction phase brings us back to dead eroded reefs on which new worms can settle (secondary settlement). This cycle seems to be independent of the age of the living population, although new settlements of young worms and also sufficient hydrodynamics seem necessary.  相似文献   
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