Plant mineral nutrition in ancient landscapes: high plant species diversity on infertile soils is linked to functional diversity for nutritional strategies

By H. Lambers, Mark C. Brundrett, J. Raven, S. Hopper. Plant and Soil, 2010

291 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/10f8f7eb1bb195bad0662c1d39f1f70c6fad5870

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Citations in the corpus

Consortium of endophyte and rhizosphere phosphate solubilizing bacteria improves phosphorous use efficiency in wheat cultivars in phosphorus deficient soils (2020, background): “Mining strategies enhance the kinetics of P adsorption/desorption reactions, solubilization of inorganic P compounds or mineralization of organic P, using root exudates (protons, organic anions and phosphatases) (Richardson et al., 2011; Lambers et al., 2010).”
The agronomic relevance of arbuscular mycorrhizas in the fertility of Australian extensive cropping systems (2012, background): “However, plants have a large range of adaptations, other than AMF, to ensure adequate P nutrition under hot, dry summer conditions (Handreck, 1997; Lambers et al., 2010; Pang et al., 2010a,b; Lambers et al., 2011).”
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): “Plants generally reduce foliar P concentration in response to low soil P availability (Crews et al. 1995; Richardson, Allen & Doherty 2008; Fyllas et al. 2009; Hidaka &Kitayama 2009; Lambers et al. 2010).”
From North to South: A latitudinal look at legume nodulation processes (2013, background): “There has been much attention given to the ways in which plants of the SWAFR cope with their impoverished soils, with most of the experimental data being on phosphorus and its acquisition in non-legumes (Lambers et al., 2011).”
Experimental assessment of nutrient limitation along a 2‐million‐year dune chronosequence in the south‐western Australia biodiversity hotspot (2012, background): “White lupin was selected as a phytometer species in this study due to its cluster roots (Gardner, Parbery & Barber 1981), a nutrient-uptake strategy shared by many native plants in our study system (Lambers et al. 2010).”
Ectomycorrhizal fungi: the symbiotic route to the root for phosphorus in forest soils (2011, background): “Indeed, even in instances where total soil P is not particularly scarce, the differential abilities of ECM fungi to enhance P acquisition by their hosts from the various soil pools may be important in competitive interactions between plants (Lambers et al. 2010).”
Which plant traits determine abundance under long‐term shifts in soil resource availability and grazing intensity? (2012, background): “specific root length, average rooting depth, presence of specialized root structures) could be very important in determining community structure, especially in nutrient-poor soils (Aerts 1999; Lambers et al. 2010).”
Beyond species: functional diversity and the maintenance of ecological processes and services (2011, background): “Journal of Applied Ecology 2011 British Ecological Society, Journal of Applied Ecology explain the tendency for nutrient poor soils to foster high species diversity (Lambers et al. 2010).”
Impacts of Nitrogen and Phosphorus: From Genomes to Natural Ecosystems and Agriculture (2017, background): “In nature excessive loadings of N and P are extrinsic drivers that (i) often reduce biodiversity directly (Chapin et al., 2000; Erisman et al., 2008; Lambers et al., 2010), and have indirect effects through (ii) increased local extinction via dominance of a few competitive species, leading to (iii)…”