Stay‐green: A consequence of the balance between supply and demand for nitrogen during grain filling?

By Andrew Borrell, Graeme L. Hammer, Erik J. van Oosterom. 2001

316 citations recorded by the source corpus.

Subfields: Agronomy and Crop Science, Plant Science

View Paper: https://www.semanticscholar.org/paper/768c4aa3588a0d1700e49f0671ee52b158dc6d8e

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Citations in the corpus

The molecular analysis of leaf senescence--a genomics approach. (2002, background): “used in some cereal improvement programmes (Borrell et al., 2001; Thomas and Howarth, 2000).”
Heat Stress in Wheat during Reproductive and Grain-Filling Phases (2011, background): “Certain stay-green sorghum genotypes have been found to contain higher specific leaf nitrogen contents, indicating that this trait is correlated with shoot nitrogen content (Borrell et al., 2001).”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, unknown): “A few tentative physiological explanations for the staygreen phenotype have been attributed to higher cytokinin levels and/or reduced ethylene production or perception (Thomas and Howarth, 2000) or higher N assimilation (Borrell et al., 2001; and reviewed in Hirel et al. 2007).”
Nitrogen partitioning and remobilization in relation to leaf senescence, grain yield and grain nitrogen concentration in wheat cultivars ☆ (2014, background): “…tay-green, the ability to retain green area during grain filling, has een related to the N supply-demand balance during grain fillng in sorghum (Borrell et al., 2001; Van Oosterom et al., 2010). artre et al. (2003) suggested that N remobilization is not driven y demand for N by the grain but…”
Small temporal differences in water uptake among varieties of pearl millet (Pennisetum glaucum (L.) R. Br.) are critical for grain yield under terminal drought (2013, background): “It is interesting that among the main mechanistic hypotheses proposed thus far to explain the expression of staygreen, most have been related to plant nitrogen status (e.g., Borrell et al. 2001; Thomas and Howarth 2000) while only a few have been related to water status (Tuinstra et al. 1998).”
Plant biomass and nitrogen partitioning changes between silking and maturity in newer versus older maize hybrids (2015, background): “All rights reserved. cation (Muchow 1994; Pan et al., 1995; Borrell et al., 2001; Gallais and Coque, 2005; Coque and Gallais, 2007; Ciampitti and Vyn, 2013).”
The challenge of improving nitrogen use efficiency in crop plants: towards a more central role for genetic variability and quantitative genetics within integrated approaches. (2007, background): “…critical NUE components under N-limiting conditions in a number of crops, the transfer of knowledge should be relatively straightforward when the experimental procedures have been adapted to larger or structurally different root systems (Hochholdinger et al., 2004) grown under agronomic conditions.”
Physiological traits used in the breeding of new cultivars for water-scarce environments. (2006, background): “In a rain-out shelter experiment a stay-green hybrid retained some photosynthesis for an additional 15 days longer than a senescent hybrid counterpart (Borrell et al., 2001).”