搜索结果: 1-10 共查到“海洋生物学 phytoplankton growth”相关记录10条 . 查询时间(0.122 秒)
Nitrate–nitrite dynamics and phytoplankton growth: Formulation and experimental evaluation of a dynamic model
Nitrate–nitrite dynamics phytoplankton growth Formulation and experimental evaluation dynamic model
2014/4/4
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...
Nitrate–nitrite dynamics and phytoplankton growth: Formulation and experimental evaluation of a dynamic model
Nitrate–nitrite dynamics phytoplankton growth Formulation experimental evaluation a dynamic model
2014/4/3
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...
Comment: Temperature, nutrients, and the size-scaling of phytoplankton growth in the sea
Comment Temperature nutrients size-scaling of phytoplankton growth the sea
2014/4/4
Comment: Temperature, nutrients, and the size-scaling of phytoplankton growth in the sea。
Relationships between phytoplankton growth and cell size in surface oceans: Interactive effects of temperature, nutrients, and grazing
phytoplankton growth cell size in surface oceans Interactive effects temperature nutrients grazing
2014/4/17
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...
Nitrogen and phosphorus inputs control phytoplankton growth in eutrophic Lake Taihu, China
Nitrogen phosphorus inputs control phytoplankton growth eutrophic Lake Taihu
2014/4/16
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...
Vitamin B12 and iron colimitation of phytoplankton growth in the Ross Sea
Vitamin B12 iron colimitation phytoplankton growth Ross Sea
2014/4/22
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...
On the nonlinear relationship between dissolved cadmium and phosphate in the modern global ocean: Could chronic iron limitation of phytoplankton growth cause the kink?
On the nonlinear relationship dissolved cadmium and phosphate the modern global ocean chronic iron limitation phytoplankton growth
2014/5/4
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 enrichments in the northeastern subarctic Pacific: Ligand production and zinc availability in response to phytoplankton growth
Iron and zinc enrichments northeastern subarctic Pacific Ligand production and zinc availability response to phytoplankton growth
2014/5/13
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 ...
Phytoplankton growth rates in the Atlantic subtropical gyres
Phytoplankton growth rates Atlantic subtropical gyres
2014/5/8
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...
A comparison of two N-irradiance interaction models of phytoplankton growth
two N-irradiance interaction models phytoplankton growth
2014/6/10
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...