The role of biomass allocation in the growth response of plants to different levels of light, CO2, nutrients and water : a quantitative review
By Hendrik Poorter, O. Nagel. 2000
232 citations recorded by the source corpus.
Subfields: Agronomy and Crop Science, Global and Planetary Change, Plant Science
View Paper: https://www.semanticscholar.org/paper/e070f72cf2280d8513dd94b464f833f68045617d
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In Agronomy and Crop Science
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Citations in the corpus
- Survival and reproduction of plant species in the Qinghai–Tibet Plateau (2014, background): “Like many other mountain areas (e.g., Charlesworth & Charlesworth, 1981; Poorter & Nagel, 2000; Poorter et al., 2012), the QTP offers an excellent system for studying resource allocation patterns in plant species due to its extreme climatic and geomorphological diversity.”
- Responses of common and rare aliens and natives to nutrient availability and fluctuations (2017, background): “…in the relative allocation of biomass to the root system, which is in line with predications of resource-limitation theory, posing that plants should allocate biomass to structures that help them acquire more of the most limiting resource (Bloom, Chapin & Mooney 1985; Poorter & Nagel 2000).”
- Intra-specific variability in biomass partitioning and carbon isotopic discrimination under moderate drought stress in seedlings from four Pinus pinaster populations (2010, methodology): “Differences in slopes and intercepts for the four populations and two watering regimes were tested by a parallelism test (Poorter and Nagel 2000).”
- Phenotypic variation in growth and biomass distribution for two advanced-generation pedigrees of hybrid poplar (2005, background): “As a result, inferences are limited, and there is a need to examine growth and biomass distribution using a larger number of clones, preferably from structured pedigrees (Stettler and Bradshaw 1994), focusing not only on phenotypic variation among clones, but also on identifying loci responsible for”
- Responses of temperate woody seedlings to shade and drought: do trade‐offs limit potential niche differentiation? (2004, methodology): “The plasticities of biomass allocation traits were calculated using quotients (Table 2), so that a greater quotient typically corresponded to larger plasticity, according to patterns found in previous work (Veneklaas and Poorter 1998, Poorter and Nagel 2000, Valladares et al. 2002).”
- Nutrient Addition Differentially Affects Ecological Processes of Avicennia germinans in Nitrogen versus Phosphorus Limited Mangrove Ecosystems (2007, background): “In many plant species, increases in growth rates with relief of nutrient limitations are achieved through greater investment in leaf tissue and reduced investment in stems and roots (Poorter and Nagel 2000).”
- Responses of wetland graminoids to the relative supply of nitrogen and phosphorus (2004, background): “For example, RMR and SLA are negatively correlated with growth rates across light levels but positively across nutrient levels Poorter and Nagel 2000 .”
- Understanding plant responses to drought - from genes to the whole plant. (2003, unknown): “Most of the drought-avoidance responses enable plant adjustment to low resources (water and minerals) (Lambers et al. 1998; Poorter and Nagel 2000).”
- Morphology and response of roots of pasture species to phosphorus and nitrogen nutrition (2006, unknown): “Root mass fraction (RMF; fraction of root dry matter as a proportion of total plant dry matter) was calculated from root mass data (present paper) and shoot mass data (Hill et al., 2005), and was used in preference to root: shoot ratio (Poorter and Nagel, 2000).”