Biological stoichiometry of plant production: metabolism, scaling and ecological response to global change.

By James J. Elser, William F. Fagan, A. Kerkhoff, N. Swenson, Brian J. Enquist. New Phytologist, 2010

953 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Nature and Landscape Conservation, Plant Science

View Paper: https://www.semanticscholar.org/paper/02cef75245643dbdf0e6c255e5b1a2b608118782

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In Global and Planetary Change

In Nature and Landscape Conservation

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Citations in the corpus

C:N:P stoichiometry of Artemisia species and close relatives across northern China: unravelling effects of climate, soil and taxonomy (2015, background): “Species identity and growth form impose a variety of structural- and size-related constraints on construction and metabolism and subsequently on stoichiometry (Elser et al. 2010).”
Species‐specific responses of foliar nutrients to long‐term nitrogen and phosphorus additions in a lowland tropical forest (2014, background): “30) to decline towards those found in high-latitude, putatively Nlimited plants (i.e. <14, Reich & Oleksyn 2004; Elser et al. 2010).”
The elemental stoichiometry of aquatic and terrestrial ecosystems and its relationships with organismic lifestyle and ecosystem structure and function: a review and perspectives (2011, background): “:P ratios range from 5 to 65 with a mean of 28–30 (Elser et al. 2000b, 2010).”
Stoichiometry of potassium is largely determined by water availability and growth in Catalonian forests (2012, background): “The growth rate hypothesis (GRH), one of the central paradigms of ecological stoichiometry (Elser et al. 1996, 2010), proposes that growing organisms must increase their allocation of P to RNA to meet the elevated demands for protein synthesis associated with growth.”
Allocation of foliar phosphorus fractions and leaf traits of tropical tree species in response to decreased soil phosphorus availability on Mount Kinabalu, Borneo (2011, background): “:P ratios are indeed associated with plant growth rates based on the GRH (Ågren 2004; Niklas & Cobb 2005; Niklas et al. 2005; Reef et al. 2010).”
Paradigm shift in plant growth control. (2015, background): “Basic stoichiometric laws do not permit significant departures from element ratios, specific for certain tissue types and plant species [21–25] and these constraints even include C incorporation in soil humus (e.”
Connecting the green and brown worlds . allometric and stoichiometric predictability of above- and below-ground networks (2013, background): “Assessed individ- ually, foliar N did not show a latitudinal trend (Elser et al., 2007, 2010; Reich and Oleksyn, 2004), unlike foliar P and foliar and litter N”
Effects of nitrogen and phosphorus supply on growth rate, leaf stoichiometry, and nutrient resorption of Arabidopsis thaliana (2014, neutral): “5b), consistent with the predictions of the relative resorption hypothesis proposed by Han et al. (2013). NRE and PRE should be tightly coupled because N and P functionally interact with each other (Ågren 2008; Güsewell 2004, 2005b; Han et al.”