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We used chemical data (3,907 lakes) and phytoplankton biomass (chlorophyll a) data (225 lakes) from Swedish lake monitoring programs to assess the effects of atmospheric nitrogen (N) deposition on nut...
We determined lysis rates of phytoplankton cells in Lake Kinneret and in lake-water microcosms by measuring the activities of particle-associated and dissolved esterases and the decay rate of the latt...
Reported estimates of phytoplankton growth rate (μ) in the subtropical gyres range widely from 0.1-0.2 to 1-2 d-1. Dividing chlorophyll a (Chl a)-normalized photosynthesis (PB) by the phytoplankton ca...
Low inorganic phosphorus (SRP) concentrations and high inorganic nitrogen to phosphorus ratios suggest that phytoplankton production in the northwestern Sargasso Sea may be controlled to some extent b...
Because of recent findings that Fe is a limiting factor for phytoplankton activity even at relatively high dissolved iron (DFe) concentrations, the potential importance of Fe limitation was revisited ...
Glutathione is an abundant intracellular thiol that is involved in the detoxification of reactive oxygen species generated in the presence of light. We used short-term continuous cultures of Emiliania...
We assessed relationships between phytoplankton standing stock, measured as chlorophyll a (Chl a), primary production (PP), and heterotrophic picoplankton production (HPP), in the epipelagic zone (0-1...
The impacts of global warming on aquatic ecosystems are expected to be most pronounced at higher trophic levels in cold-water environments. Therefore, we hypothesized that warming of fishless alpine p...
Changes in the size and neutral aldose (NAld) composition of phytoplankton photosynthetic products during the early diagenetic process were experimentally examined using 13C as a tracer. Most (94.7%) ...
The potentially toxic element selenium is first concentrated from solution to a large but highly variable degree by algae and bacteria before being passed on to consumers. The large loads of abiotic a...
The outputs of simple models relating phytoplankton growth and chlorophyll a (Chl a) to irradiance and nutrient (nitrogen [N] and/or iron [Fe]) availability are compared with those of complex mechanis...
To establish the influence of phytoplankton blooms on the cycling of dissolved and particulate species of organic carbon and nitrogen, we conducted a field study during a series of blooms in a coastal...
In the Gulf of Aqaba, the northeasternmost segment of the Red Sea, phytoplankton blooms are more intense than in other oligotrophic regions (e.g., the Sargasso Sea). In this study, we use multiyear in...
Variability in upper ocean optical properties is often driven by changes in the particle pool. We investigated the effects of such changes by characterizing individual particles. For particles in natu...
Our understanding of the dynamics of phytoplankton communities has been limited by the space and timescales associated with traditional monitoring approaches. To overcome some of these limitations, we...

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