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A multi-nutrient quota model was modified to describe the coupled dynamics of nitrate and nitrite utilization for four phytoplankton species, Picochlorum atomus (Butcher) (Chlorophyta), Nannochloropsi...
A multi-nutrient quota model was modified to describe the coupled dynamics of nitrate and nitrite utilization for four phytoplankton species, Picochlorum atomus(Butcher) (Chlorophyta), Nannochloropsis...
We analyzed long-term (5–8 yr) hourly time series of chlorophyll (Chl) converted from fluorescence measurements in relation to discharge and light in three medium- to large-size rivers, where plankton...
Comment: Temperature, nutrients, and the size-scaling of phytoplankton growth in the sea。
We compile two data sets from14C uptake and dilution experiments conducted in surface waters of the global ocean to investigate the relationship between phytoplankton mass-specific growth rate and cel...
Lake Taihu (Taihu) is the third largest freshwater lake in China and an important drinking water, fishing, and tourism resource for Jiangsu Province. Recent toxic cyanobacterial blooms caused by exces...
We conducted 28 dilution experiments during August–September 2007 to investigate the coupling of growth and microzooplankton grazing rates among ultraphytoplankton populations and the phytoplankton c...
Primary production in the Ross Sea, one of the most productive areas in the Southern Ocean, has previously been shown to be seasonally limited by iron. In two of three bottle incubation experiments co...
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...
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 ...
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...
Phytoplankton growth and stoichiometry depend on the availability of multiple nutrients. We use a mathematical model of phytoplankton with flexible stoichiometry to explain patterns of phytopla...
We present an analysis of the global impact of microplanktonic grazers on marine phytoplankton and its implications for remineralization processes in the microbial community. The data were obtained by...
Near-surface seawater from the northeastern subarctic Pacific was incubated on deck for 8 d, supplemented with (1) control, no additions (2) 1Zn (3) 1Fe (4) 1Zn1Fe. Concentrations of total Zn a...
The N-photoacclimation interaction models of Geider et al. (GM) and Flynn et al. (FM) are compared by tuning them to data from a light-shift experiment for a diatom. Both the original model constructs...

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