Plant Strategies, Vegetation Processes, and Ecosystem Properties

By D. Aplin. 2002

251 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/06301a360f8d6428b49484a65208df6973503ac8

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Citations in the corpus

Refining the stress‐gradient hypothesis for competition and facilitation in plant communities (2009, unknown): “uptake rates of the benefactor compared to the beneficiary species (Grime 2001).”
Allocating CSR plant functional types: the use of leaf economics and size traits to classify woody and herbaceous vascular plants (2013, unknown): “As predicted by Grime (2001), woody species occupied a region of the CSR triangle from S (typically gymnosperm trees or angiosperm bushes), through CS (angiosperm trees and woody lianas) to C (angiosperm trees with larger leaves): that is S ?”
Causal networks clarify productivity–richness interrelations, bivariate plots do not (2014, background): “He argues, instead, that relationships in the Adler et al. data are actually strong and, further, that failure to adhere to the humped-back model (HBM; sensu Grime 1979) threatens scientists’ ability to advise conservationists.”
Now you See them, Now you don't! – Population Crashes of Established Introduced Species (2004, background): “Or an introduced plant may produce an allelopathic chemical that remains in the soil long after the plant has disappeared (see, e.g., Rice 1984; Grime 2001).”
Predicting changes in community composition and ecosystem functioning from plant traits: revisiting the Holy Grail (2002, methodology): “Although precursors of this framework have been presented previously (Chapin et al. 2000; Díaz et al. 1999; Grime 2001), we have now linked disconnected conceptual elements and a suite of empirical data.”
Impact of different meadow mowing techniques on field invertebrates (2010, background): “Agricultural grasslands are disturbance-dependent habitats, and one or two cuts per year are usually considered beneficial to meadow plant diversity (Huston 1994; Grime 2001; Antonsen and Olsson 2005).”
Plant functional types: are we getting any closer to the Holy Grail? (2007, background): “For the resource axis it showed that responses to resource availability and effects on biogeochemistry are jointly constrained by the trade-off between acquisition and conservation strategies, and their characteristic traits (Chapin et al. 1993, Grime 2001).”
Seedling Ecology and Evolution: Seedling morphology, evolution, and physiology (2008, background): “Additional information about regeneration strategies may be found in Harper (1977), Grubb (1977, 1998), and Grime (2001).”
Competition increases with abiotic stress and regulates the diversity of biological soil crusts (2010, background): “Operating concurrently with these forces, plant competition generally manifests as competition for water and nutrients in the rhizosphere, or competition for light in the canopy (Grime 2001).”
Biodiversity Regulation of Ecosystem Services (2005, background): “In nature, therefore, high species diversity and high productivity are often not positively correlated (Grime 1979, 2001; Gough et al. 1994; Waide et al. 1999).”
Is successional research nearing its climax? New approaches for understanding dynamic communities (2015, methodology): “Secondary succession on fertile substrate typically promotes early dominance by high resource demanding herbs that are able to usurp light and soil resources and that strongly inhibit woody colonization (Grime 2001).”
What do the biodiversity experiments tell us about consequences of plant species loss in the real world (2004, unknown): “Dispersal syndromes are only vaguely dependent on the established strategies (Grime, 2001).”
The resource availability hypothesis revisited: a meta‐analysis (2011, background): “Our results are consistent with the well-established fact that species growth rates vary with fertility levels (Grime 2001) and light requirements (Swaine & Whitmore 1988).”