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Colimitation of the unicellular photosynthetic diazotroph Crocosphaera watsonii by phosphorus, light, and carbon dioxide
Colimitation unicellular photosynthetic diazotroph Crocosphaera watsonii phosphorus, light carbon dioxide
2014/4/2
We describe interactive effects of total phosphorus (total P = 0.1–4.0 μmol L−1; added as H2NaPO4), irradiance (40 and 150 μmol quanta m−2 s−1), and the partial pressure of carbon di...
A model of phytoplankton acclimation to iron–light colimitation
phytoplankton acclimation iron–light colimitation
2014/4/16
We developed and calibrated a dynamic model for cellular carbon, chlorophyll (Chl), and iron under iron–light
colimitation. The model allows growth rate and two other state variables (Fep
: C and Ch...
Colimitation of decomposition by substrate and decomposers – a comparison of model formulations
Colimitation decomposition substrate decomposers model formulations
2010/1/15
Decomposition of soil organic matter (SOM) is limited by both the available substrate and the active decomposer community. The understanding of this colimitation strongly affects the understanding of ...
Zinc-cobalt colimitation of Phaeocystis antarctica
Zinc-cobalt colimitation Phaeocystis antarctica
2014/4/21
We present evidence demonstrating the capability of Phaeocystis antarctica colonies to substitute cobalt (Co) and zinc (Zn) as micronutrients, in which Co limitation is alleviated by additions of Zn a...
Some thoughts on the concept of colimitation: Three definitions and the importance of bioavailability
Some thoughts the concept of colimitation Three definitions bioavailability
2014/4/21
We discuss the concept of colimitation of primary productivity in aquatic environments, with an emphasis on reconciling this concept with recent advances in marine bioinorganic chemistry. Colimitation...
Some thoughts on the concept of colimitation: Three definitions and the importance of bioavailability
concept of colimitation Three definitions mportance of bioavailability
2014/4/18
We discuss the concept of colimitation of primary productivity in aquatic environments, with an emphasis on reconciling this concept with recent advances in marine bioinorganic chemistry. Colimitation...
Zinc-cobalt colimitation of Phaeocystis antarctica
Zinc-cobalt colimitation Phaeocystis antarctica
2014/4/18
We present evidence demonstrating the capability of Phaeocystis antarctica colonies to substitute cobalt (Co) and zinc (Zn) as micronutrients, in which Co limitation is alleviated by additions of Zn a...
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...
Evidence for phosphorus, nitrogen, and iron colimitation of phytoplankton communities in Lake Erie
Evidence for phosphorus nitrogen iron colimitation of phytoplankton communities Lake Erie
2014/4/22
Three nutrient enrichment experiments involving the addition and removal of iron (Fe) alone, as well as in combination with phosphorus (P) and/or nitrogen (N), were conducted in the offshore and nears...
Zinc-bicarbonate colimitation of Emiliania huxleyi
Zinc-bicarbonate colimitation Emiliania huxleyi
2014/5/21
In analogy to the Fe hypothesis, the Zn hypothesis states that Zn may limit primary production in some regions
of the world oceans and therefore influence the global carbon cycle. The proposed ...