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I report two vertical profiles of dissolved cadmium (Cd) and phosphate (PO4) from the Bering Sea: one from a high-nutrient, low-chlorophyll (HNLC) area, in which phytoplankton growth is limited by iro...
During the European Iron Fertilisation Experiment (EIFEX), performed in the Southern Ocean, we investigated the reactions of different phytoplankton size classes to iron fertilization, applying measur...
A cross-ecosystem comparison of data obtained from 92 coastal zone ecosystems worldwide revealed a strong positive response of marine phytoplankton biomass to nutrient enrichment that is highly consi...
Phytoplankton response to nutrients was examined with a 26-yr database from the Delaware Estuary. Biomassnormalized primary production did not increase linearly with increasing nutrient concentrations...
We report the first direct measurements of the contribution of phytoplankton and bacterial cells to the measured alkalinity of unfiltered seawater. Phytoplankton and bacterial cells suspe...
Resource distributions in the ocean are heterogeneous in time and space. Theory predicts planktonic predators may exploit these resource patches by modifying their movements in response to mechanical...
We investigated the carbon acquisition of three marine microalgae, Skeletonema costatum, Phaeocystis globosa, and Emiliania huxleyi in response to different light regimes. Rates of photosynthetic O2 ...
Phytoplankton carbon (C) and nitrogen (N) content is commonly normalized to phosphorus (P) quotas as Redfield C:N: P ratios. We examined how surface-bound P pools affect Redfield stoichiometry and P u...
We performed dilution experiments and primary production measurements in surface waters during a cruise in the northwestern Mediterranean Sea in June 2000 to quantify the carbon (C) flux through phyto...
Under high nutrient concentrations and sufficient light conditions, large phytoplankton may display higher photosynthetic efficiency than smaller cells. This is unexpected since smaller phytoplankton,...
Iron- and zinc-enrichment experiments were carried out at Ocean Station Papa in the subarctic North Pacific. In iron-enriched treatments, phytoplankton chlorophyll a (Chl a) increased 20-fold (9.7 μg ...
The Continuous Plankton Recorder (CPR) survey has been used to characterize phytoplankton and zooplankton space-time dynamics in the North Sea since 1931 and in the North Atlantic since 1939. Phytopla...
We developed an absorption-based primary production model that includes the effects of phytoplankton community size structure for the continental margin and adjoining Gulf Stream waters of the Middle ...
We report the results of a field study, in productive waters off California, of the factors that control the particulate cadmium (Cd) : phosphorus (P) composition of natural assemblages of marine phyt...
We examined the interannual variability in the timing and magnitude of seasonal phytoplankton blooms in the North Atlantic (708N–108N, 908W–108E) in relation to variability in wind forcing during the...

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