The nutritional control of root development

By B. Forde, H. Lorenzo. Plant and Soil, 2001

527 citations recorded by the source corpus.

Subfields: Plant Science

View Paper: https://www.semanticscholar.org/paper/5c5a79f1616c64753267fe48e8925cc6350ab588

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Plant Science

1. J. Lynch
2. P. White
3. K. Brown
4. J. Barea
5. P. Hinsinger
6. A. Richardson
7. C. Plassard
8. John Hammond

Citations in the corpus

• A dynamic root system growth model based on L-Systems (2010, methodology): “…to resource heterogeneity in the soil are subject to ongoing empirical research concerning phytohormone mediated signalling pathways and species specific morphological and physiological reactions (e.g. Forde and Lorenzo 2001; Callaway et al. 2003; Hodge 2004; Zhang et al. 2007; Peret et al. 2009).”
• Vertical Vegetation Structure Below Ground: Scaling from Root to Globe (2005, background): “Local proliferation tends to be strongest in patches containing nutrients most limiting to plant growth, such as nitrogen and phosphorus (Robinson 1994; Robinson and van Vuuren 1998; Forde and Lorenzo 2001).”
• Functional biology of plant phosphate uptake at root and mycorrhiza interfaces. (2007, background): “Root development is remarkably sensitive to variations in the supply and distribution of P in the soil (Wiersum, 1958; Forde & Clarkson, 1999; Forde & Lorenzo, 2001) and roots respond in many ways to altering P availability, for example by changes in root architecture (López-Bucio et al ., 2003),…”
• Nutrient Sensing and Signalling in Plants: Potassium and Phosphorus (2005, background): “initiation and growth of lateral (Chevalier et al., 2003; Forde and Lorenzo, 2001; Lynch and Brown, 2001; Malamy, 2005) or cluster roots (Dinkelaker et al.”
• Acquisition of phosphorus and nitrogen in the rhizosphere and plant growth promotion by microorganisms (2009, background): “Whilst primary root growth is generally less sensitive to nutritional effects than is the growth of secondary or higher root orders (Forde and Lorenzo 2001), the diameter of first and second order laterals were significantly thicker in cereals grown at high concentrations of NO3 − (Drew et al.”
• Modelling diverse root density dynamics and deep nitrogen uptake—A simple approach (2009, background): “The development and proliferation of the roots in soil are affected by intrinsic and extrinsic parameters such as the supply of photosynthates from the shoot, the nutrient status of the plant, soil type and compaction, water potential at the root surface and availability and distribution of nutrient”
• ROOT STRATEGIES FOR PHOSPHORUS ACQUISITION (2008, background): “However, increased SRL could result from the increased proportion of secondary roots, since comparisons are not usually made within root classes (Eissenstat et al. 2000; Forde and Lorenzo 2001).”
• Intrinsic and environmental response pathways that regulate root system architecture. (2005, background): “2003) and root system responses to nutrients (Forde & Lorenzo 2001; LopezBucio, Cruz-Ramirez & Herrera-Estrella 2003).”
• Plant morphology and root hydraulics are altered by nutrient deficiency in Pistacia lentiscus (L.) (2006, background): “Some plant strategies to cope with drought, such as increased biomass allocation belowground, increased WUE or changes in root morphology (Ingestad and Ågren 1991; Jackson et al. 2000) have been described for nutrient-limited plants (Forde and Lorenzo 2001).”
• Effects of rhizobacterial ACC deaminase activity on Arabidopsis indicate that ethylene mediates local root responses to plant growth-promoting rhizobacteria (2008, background): “By contrast, lateral root development, which process is integrated at the whole plant level and involves systemic regulation by shoot-derived compounds [78], appears not to be affected by the AcdS activity of rhizosphere colonizing bacteria.”
• Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, unknown): “The transcript abundance was normalized against peanut Ubiquitin (Luo et al. , 2005) transcript levels.”
• The role of nutrient availability in regulating root architecture. (2003, background): “The development of root systems is usually highly asymmetric and reflects the ability of roots to adjust their growth and development to environmental factors [3,4 ].”