Models of multiple potentially limiting nutrients currently employ either multiplicative or threshold formulations, neither of which has a sound mechanistic explanation. Despite experimental evidence that lack of P severely constrains N assimilation, this mechanism has not been considered for constructing models of multi-nutrient limitation. We construct a phytoplankton optimal growth model linking C, chlorophyll (Chl), N, and P through a limitation chain in which P limits N assimilation, N limits photosynthesis and photosynthesis limits growth. The resulting formulation possesses characteristics of both multiplicative and threshold approaches and provides a mechanistic foundation for modelling multi-nutrient and light limitation of phytopl...
In this paper we have proposed and analyzed a simple mathematical model consisting of four variables...
To increase the efficiency of computing phytoplankton growth rate (μ), chlorophyll-to-carbon (θ) and...
Phytoplankton cell size influences particle sinking rate, food web interactions and biogeographical...
Phytoplankton growth and stoichiometry depend on the availability of multiple nutrients. We use a ma...
The widely used concept of constant ”Redfield” phytoplankton stoichiometry is often applied for esti...
The elemental ratios of marine phytoplankton emerge from complex interactions between the biotic and...
The aim of this study is to evaluate the consequences of accounting for variable Chl:C (chlorophyll:...
© 2014, Springer International Publishing Switzerland. Phosphorus (P) limitation has been regarded a...
The aim of this study is to evaluate the consequences of accounting for variable Chl:C (chlorophyll:...
Marine phytoplankton can regulate their stoichiometric composition in response to variations in the ...
International audienceThe aim of this study is to evaluate the consequences of accounting for variab...
We try to answer the question of to what extent details in nutrient uptake and phytoplankton physiol...
There is a long-established, remarkable correspondence between the nitrogen-to-phosphorus ratio N:P~...
In this paper we have proposed and analyzed a simple mathematical model consisting of four variables...
In this paper we have proposed and analyzed a simple mathematical model consisting of four variables...
To increase the efficiency of computing phytoplankton growth rate (μ), chlorophyll-to-carbon (θ) and...
Phytoplankton cell size influences particle sinking rate, food web interactions and biogeographical...
Phytoplankton growth and stoichiometry depend on the availability of multiple nutrients. We use a ma...
The widely used concept of constant ”Redfield” phytoplankton stoichiometry is often applied for esti...
The elemental ratios of marine phytoplankton emerge from complex interactions between the biotic and...
The aim of this study is to evaluate the consequences of accounting for variable Chl:C (chlorophyll:...
© 2014, Springer International Publishing Switzerland. Phosphorus (P) limitation has been regarded a...
The aim of this study is to evaluate the consequences of accounting for variable Chl:C (chlorophyll:...
Marine phytoplankton can regulate their stoichiometric composition in response to variations in the ...
International audienceThe aim of this study is to evaluate the consequences of accounting for variab...
We try to answer the question of to what extent details in nutrient uptake and phytoplankton physiol...
There is a long-established, remarkable correspondence between the nitrogen-to-phosphorus ratio N:P~...
In this paper we have proposed and analyzed a simple mathematical model consisting of four variables...
In this paper we have proposed and analyzed a simple mathematical model consisting of four variables...
To increase the efficiency of computing phytoplankton growth rate (μ), chlorophyll-to-carbon (θ) and...
Phytoplankton cell size influences particle sinking rate, food web interactions and biogeographical...