搜索结果: 1-15 共查到“phytoplankton growth”相关记录19条 . 查询时间(0.125 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...
Phytoplankton growth in three rivers: The role of meroplankton and the benthic retention hypothesis
Phytoplankton growth three rivers The role of meroplankton the benthic retention hypothesis
<
2014/4/8
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
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...
Effects of the pH/pCO2 control method on medium chemistry and phytoplankton growth
Effects pH/pCO2 control method medium chemistry phytoplankton growth
<
2010/1/20
The control of key chemical parameters in phytoplankton cultures, such as pCO2, pH and Ω (the saturation state of calcium carbonate), is made difficult by the interdependence of these parameters and b...
Close coupling between phytoplankton growth and microzooplankton grazing in the western South China Sea
Close coupling phytoplankton growth microzooplankton grazing
<
2014/4/18
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...
Preliminary report on evaluating the effects of agricultural drainage on phytoplankton growth in Lake Biwa
phytoplankton growth bioassay
<
2009/4/1
The effects of pesticides and nutrient loading from paddy fields on the growth of natural phytoplankton assemblages collected from Lake Biwa were examined by bioassay using the waters from Lake Biwa, ...
Microzooplankton grazing and phytoplankton growth in marine mesocosms with increased CO2 levels
Microzooplankton grazing phytoplankton growth marine mesocosms CO2 levels
<
2010/1/18
Microzooplankton grazing and algae growth responses to increasing pCO2 levels (350, 700 and 1050 μatm) were investigated in nitrate and phosphate fertilized mesocosms during the PeECE III experiment 2...
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 ...
Interactive effects of temperature and nutrient limitation on the response of alpine phytoplankton growth to ultraviolet radiation
Interactive effects of temperature nutrient limitation on the response alpine phytoplankton growth ultraviolet radiation
<
2014/5/13
We performed bag-enclosure experiments for 7 d in a lake in the Beartooth Mountains (in Montana andWyoming) using natural phytoplankton assemblages. Ultraviolet radiation (UVR) (exposed or blocked), t...
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...