Dynamic Energy and Mass Budgets in Biological Systems

By Sebastiaan A. L. M. Kooijman. 2000

1,061 citations recorded by the source corpus.

Subfields: History, Literature and Literary Theory, Sociology and Political Science

View Paper: https://www.semanticscholar.org/paper/e4114f891d8d020c4d76b218cbc20b7d12a5ae1e

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Citations in the corpus

Interconnection of nitrogen fixers and iron in the Pacific Ocean: Theory and numerical simulations (2012, methodology): “…given by Dutkiewicz et al. [2009], but temperature modification is changed from that used by Dutkiewicz et al. [2009], and is based on the Arrenhius function [Kooijman, 2000]: gT ¼ t1 exp AE 1T þ 273:15 1 To where coefficients t1,AE and To regulate the form of the temperature modification function.”
Bio‐energetics underpins the spatial response of North Sea plaice (Pleuronectes platessa L.) and sole (Solea solea L.) to climate change (2012, background): “Species differences are described by species-specific traits (values of model parameters) that determine the relative amounts of energy directed to different processes as well as the tolerance levels to environmental factors (Kooijman, 2000, 2010; Freitas et al., 2011).”
A comparison of scope for growth (SFG) and dynamic energy budget (DEB) models applied to the blue mussel (Mytilus edulis) (2011, methodology): “We have adapted the DEB symbols and notations from Kooijman (2000), where braces {} denote quantities expressed as per unit surface-area of the structural volume and first derivatives with respect to time are indicated with overdots.”
Modelling the cultivation and bioremediation potential of the kelp Saccharina latissima in close proximity to an exposed salmon farm in Norway (2013, background): “…area specific growth and uptake rates (μ and J, respectively): (4) Here, T1 and TArr are reference and Arrhenius temperatures (°K), respectively (e.g. Kooijman 2000), while μmax and Jmax are the maximal area-specific growth and uptake rates as functions of the present growth model state variables…”
Relationship between symbiont density and photosynthetic carbon acquisition in the temperate coral Cladocora caespitosa (2010, background): “This is based on the concept that conditions that allow maximal energy acquisition also maximize organism growth, reproduction, and survival (e.g., Kooijman 2000).”
Energetics approach to predicting mortality risk from environmental stress: a case study of coral bleaching (2009, background): “A growing number of studies have used energetics as a framework for linking sub-organism processes to population ecology in unitary organisms (Noonburg et al. 1998; Koiijman 2000; Nisbet et al. 2000, 2004).”
Optimal nitrogen-to-phosphorus stoichiometry of phytoplankton (2004, background): “Others have modelled carbon allocation to different cellular component”
Modelling trace metal (Hg and Pb) bioaccumulation in the Mediterranean mussel, Mytilus galloprovincialis , applied to environmental monitoring (2006, methodology): “Kooijman (2000) introduced a threshold value of the structural volume VP which marks the transition between development and gamete production and showed that: ( ) [ ]Mp pVVpdtdR C && ⋅⋅−−⋅−= ),min(1)1( κκκ (J.d-1) [5] Spawning was triggered at a given date corresponding to observations of dramatic…”