Solute Movement in the Rhizosphere
By P. Tinker, P. Nye. 2000
602 citations recorded by the source corpus.
Subfields: Plant Science
View Paper: https://www.semanticscholar.org/paper/a701116e24a5d5e84a0f2336b511f4b6d3fa1a61
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In Plant Science
Citations in the corpus
- A dynamic model for the combined effects of N, P and K fertilizers on yield and mineral composition; description and experimental test (2007, methodology): “These and a number of other soil chemical processes can affect nutrient availability (Tinker and Nye 2000).”
- Acquisition of phosphorus and nitrogen in the rhizosphere and plant growth promotion by microorganisms (2009, background): “Orthophosphate is rapidly depleted in the immediate vicinity of plant roots, and as such a large concentration gradient occurs across the rhizosphere between bulk soil and the root surface (Gahoonia and Nielsen 1997; Tinker and Nye 2000; Fig.”
- Effects of Root Exudates in Microbial Diversity and Activity in Rhizosphere Soils (2008, background): “The role of phosphatases in the rhizosphere remains uncertain (Tinker and Nye 2000).”
- Plant species traits and capacity for resource reduction predict yield and abundance under competition in nitrogen‐limited grassland (2006, background): “Journal compilation © 2006 British Ecological Society Blackwell Publishing LtdPlant species traits and capacity for resource reduction predict yield and abundance under competition in nitrogen-limited grassland J. FARGIONE*† and D. TILMAN”
- A dynamic root system growth model based on L-Systems (2010, background): “The root system grew in a pot with a bottom radius of 3 cm, a top radius of 5 cm and a height of 10 cm. Model parameters were taken from liter- ature and represent typical values for phosphate uptake from soil by maize (Tinker and Nye 2000; Föhse et al. 1991).”
- Plant mechanisms to optimise access to soil phosphorus (2009, background): “Characteristics of roots (Table 1) that assist exploration of soil and P acquisition include: high rootmass ratio (i.e. a large rootmass as a proportion of total plant mass; Tinker and Nye 2000), high root elongation rate (Silberbush and Barber 1983; Wissuwa 2003), high specific root length or ‘SRL’”
- Modelling the rhizosphere: a review of methods for ‘upscaling’ to the whole‐plant scale (2006, methodology): “…is the volumetric water content of the soil, u is the Darcy flux of water and D is the diffusion coefficient of nutrient in the pore solution (¼ DLf where DL is the diffusion coefficient in water and f is the diffusion impedance factor; Tinker & Nye 2000), t is time and ds is defined below.”
- Mechanisms of plant competition for nutrients, water and light (2013, background): “If we assume that uptake is a linear function of the supply per unit root length over low nutrient supplies (Tinker & Nye 2000), then over this range fðSLÞ ¼ SL AllocR SRL NR½ eqn 3 where AllocR is the relative allocation of acquired nutrients to root biomass, [NR] is the nutrient concentration of…”
- Mycorrhizal Fungi Can Dominate Phosphate Supply to Plants Irrespective of Growth Responses1 (2003, background): “…contribution to total P uptake have often assumed that the direct and mycorrhizal uptake pathways act in concert, although it is recognized that uptake directly from soil may decrease as the concentration of P in the soil solution adjacent to the roots becomes depleted (Tinker and Nye, 2000).”
- Arbuscular Mycorrhizal Mediated Nutrition in Plants (2009, background): “This can at least partially be attributed to the assumption that AM fungi have little capacity to enhance plant uptake of mobile ions such as NO3− because these ions move rapidly in soil (Tinker and Nye, 2000).”
- Trade-Offs in Arbuscular Mycorrhizal Symbiosis: Disease Resistance, Growth Responses and Perspectives for Crop Breeding (2017, positive): “In the ajority of soils, phosphate supply is li ited due to rapid i obilisation by free cations [14].”
- Ecophysiological traits associated with the competitive ability of invasive Australian acacias (2011, positive): “Mass flow of nutrients requires adequate soil water to supply transpirational demand and hence operates at the expense of WUE (Barber, 1995; Tinker & Nye, 2000; Raven et al., 2004; Cramer et al., 2009).”
- Resource Exchange in the Rhizosphere: Molecular Tools and the Microbial Perspective (2006, background): “This soil structure strongly influences general rhizosphere resource exchange (e.g., Hillel 1998, Tinker & Nye 2000).”