Root structure and functioning for efficient acquisition of phosphorus: Matching morphological and physiological traits.
By H. Lambers, M. W. Shane, M. Cramer, Stuart J. Pearse, Erik J. Veneklaas. Annals of Botany, 2006
1,287 citations recorded by the source corpus.
Subfields: Plant Science, Soil Science
View Paper: https://www.semanticscholar.org/paper/c3a55c23d9b21e27a29d2ea43024bd816f992109
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
- H. Lambers
- J. Lynch
- J. Barea
- A. Richardson
- Vincent Vadez
- F. Andrew Smith
- Erik J. Veneklaas
- P. Hinsinger
In Soil Science
- H. Lambers
- Benjamin L Turner
- Johnw. G. Cairney
- Etienne Laliberté
- P. Hayes
- F. Albornoz
- P. Hinsinger
- Richard J. Simpson
Citations in the corpus
- The role of complementarity and selection effects in P acquisition of intercropping systems (2017, background): “…to be exhausted by increased food needs in the future (Gilbert 2009), and therefore it is important to better exploit soil P resources, for example by rhizosphere management strategies to optimize P bioavailability in agro-ecosystems (Lambers et al. 2006; Zhang et al. 2010; Hinsinger et al. 2011).”
- Soil and fertilizer phosphorus in relation to crop nutrition (2008, background): “In general, a tendency to increasing acidification is the common trend in cropping systems (Lambers et al. 2006).”
- Variation in seedling growth of 11 perennial legumes in response to phosphorus supply (2010, background): “For instance, many Australian native plant species have evolved in P-impoverished soils (Handreck 1997) and have developed various mechanisms to acquire P from such soils, e.g., root clusters, mycorrhizal symbioses, exudation of carboxylates and phosphatases ( Lambers et al. 2006 ).”
- Greater root phosphatase activity in nitrogen‐fixing rhizobial but not actinorhizal plants with declining phosphorus availability (2017, background): “…production of root phosphatases used by non-legumes in this study include cluster-root formation (e.g. Brundrett & Abbott 1991; Diem et al. 2000; Lambers et al. 2006, 2008), specialising in the acquisition of soluble or insoluble inorganic forms of soil P (e.g. Lambers et al. 2008; Turner…”
- Novel approaches in plant breeding for rhizosphere-related traits (2009, background): “From a physiological perspective, a focus should be placed on traits leading to enhanced root exudation of compounds capable of solubilizing soil-bound nutrients such as P (Lambers et al. 2006), Zn (Hoffland et al. 2006) or iron (Fe; Ishimaru et al. 2006).”
- A fresh framework for the ecology of arid Australia (2011, background): “The first significant consequence in arid Australia is that nutrient-acquiring mechanisms are prominent, including heavy investment in root structures and N-fixing microbes or mycorrhizal fungi (Lambers et al., 2006); conservation is achieved through the long-lived foliage already noted.”
- Mycorrhizal associations and other means of nutrition of vascular plants: understanding the global diversity of host plants by resolving conflicting information and developing reliable means of diagnosis (2009, background): “abundant than elsewhere in the world (Lamont 1982; Lambers et al. 2006).”
- Management of soil phosphorus and plant adaptation mechanisms to phosphorus stress for sustainable crop production: a review (2012, neutral): “tion of organic anions (especially citrate and malate) and phosphatases, which help to solubilize insoluble P resources and hydrolyze organic P for plant uptake (Playsted et al., 2006; Lambers et al., 2006).”
- Phosphorus acquisition characteristics of cotton (Gossypium hirsutum L.), wheat (Triticum aestivum L.) and white lupin (Lupinus albus L.) under P deficient conditions (2008, background): “According to Lamont et al. (1984) and Pessarakli (1999), average root hair length of wheat (about 1.”
- Rhizosphere: biophysics, biogeochemistry and ecological relevance (2009, background): “Specialized organs such as ectomycorrhizal roots and cluster roots are additional sources of heterogeneities in exudation, uptake and acquisition of nutrients along root systems (Plassard et al. 2002; Casarin et al. 2003; Shane and Lambers 2005; Lambers et al. 2006).”
- Plant-microbe-soil interactions in the rhizosphere: an evolutionary perspective (2009, background): “However, it should be borne in mind that Hakea prostrata, like other cluster-bearing plants in Mediterranean environments, produces root clusters only during the wet winter months, so that the C costs on an annual basis are probably four times less (Lambers et al. 2006).”
- Ecophysiological traits associated with the competitive ability of invasive Australian acacias (2011, neutral): “Cluster roots are efficient at acquiring nutrients, particularly P from low-concentration and sparingly soluble sources (Lambers et al., 2006).”