Resource Strategies of Wild Plants

By Surya Raghu. 2011

141 citations recorded by the source corpus.

Subfields: Ecology, Ecology, Evolution, Behavior and Systematics, Forestry

View Paper: https://www.semanticscholar.org/paper/91e5307f5b2e4271a8b7a324a4707ed37fb6e888

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Citations in the corpus

A trait-based approach to comparative functional plant ecology: concepts, methods and applications for agroecology. A review (2012, unknown): “Suites of correlated traits appear to also exist in roots and represent a trade-off between root longevity and growth rate (cf. Roumet et al. 2006; Craine 2009; Freschet et al. 2010).”
Mechanisms of plant competition for nutrients, water and light (2013, background): “In simultaneously addressing competition for the three types of resources, consistent terminology is important (Craine 2009).”
The world‐wide ‘fast–slow’ plant economics spectrum: a traits manifesto (2014, background): “…and high tissue longevity, which excel at tolerating low resources and/or suppressing resource supply to neighbours, are successful under low nutrient supply (Tilman 1987; Tilman & Wedin 1991; Aerts & Chapin 2000; Craine et al. 2002; Craine 2009; Holdaway et al. 2011; Mason et al. 2012).”
Ecophysiological traits associated with the competitive ability of invasive Australian acacias (2011, unknown): “Root biomass can be preferentially allocated to enriched shallow soils and/or towards growing deeper roots to tap unused nutrient resources (Jobbágy & Jackson, 2001; Lambers et al., 2008a; Craine, 2009).”
Root nutrient concentration and biomass allocation are more plastic than morphological traits in response to nutrient limitation (2017, background): “Increasing the branching frequency of fine roots is another possible adjustment to enhance nutrient foraging capacity into resource-rich soil patches (Craine 2009; Kong et al. 2014).”
Responses of common and rare aliens and natives to nutrient availability and fluctuations (2017, background): “There is evidence that, in contrast to plants from constant environments, plants from fluctuating environments have higher nutrient-uptake rates and show a stronger increase in potential uptake rates when nutrient availability increases (Craine 2009).”
Interspecific integration of trait dimensions at local scales: the plant phenotype as an integrated network (2017, background): “Developing a general classification scheme for plant diversity based on different aspects of ecological strategies has been a central focus in plant ecology (Grime 1977; Southwood 1988; Westoby et al. 2002; Craine 2009).”
Scaling from Traits to Ecosystems: Developing a General Trait Driver Theory via Integrating Trait-Based and Metabolic Scaling Theories (2015, background): “While this has long been part of comparative physiology and ecology (see Arnold, 1983; Grime, 1977), it is now being heralded as its central paradigm (Craine, 2009; 251Scaling from Traits to Ecosystems Westoby and Wright, 2006).”
A multi‐trait test of the leaf‐height‐seed plant strategy scheme with 133 species from a pine forest flora (2010, background): “Plants are multifaceted organisms that have evolved ecolog- ical strategies for sustaining populations in resource-limited environments (Grime 1979; Craine 2009).”