Coordination of carbon supply and plant growth.

By Alison M. Smith, Mark Stitt. Plant, Cell and Environment, 2007

1,028 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/22180b53d5319d2ec12a574d4aa916c3f1781286

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Citations in the corpus

Growth and carbon relations of tree line forming conifers at constant vs. variable low temperatures (2009, background): “Clearly, due to complex feedback mechanisms between photosynthetic activity and carbon sink activities (Smith & Stitt 2007), and physiological limitations (e.g. the carrying capacity of plastids for starch granula), the accumulation of carbon reserves is not infinite and reaches an upper limit.”
Starch: its metabolism, evolution, and biotechnological modification in plants. (2010, background): “Mutant Arabidopsis plants that cannot synthesize starch, or cannot degrade it at night, have reduced growth rates under most conditions (129).”
The use of metabolomics to dissect plant responses to abiotic stresses (2012, background): “Even short periods of C starvation lead to an inhibition of growth, which is not immediately reversed when C becomes available again [94, 95].”
Recovery following defoliation involves shifts in allocation that favour storage and reproduction over radial growth in black oak (2017, background): “…under stressful conditions as a mechanism to avoid carbon starvation, where there is insufficient carbon supply for the metabolism, defence and hydraulic maintenance necessary for sustaining life (Smith & Stitt 2007; McDowell & Sevanto 2010; Sala, Woodruff & Meinzer 2012; Wiley & Helliker 2012).”
Some aspects of citrus ecophysiology in subtropical climates: re-visiting photosynthesis under natural conditions (2007, background): “This is accomplished by regulating the partitioning of photoassimilates, starch degradation at night and plant growth in a changing environment, as occurs during the seasonal variation of in light and water availability, day length and temperature (Smith and Stitt, 2007).”
Species-specific water use by forest tree species: from the tree to the stand (2012, background): “, 2001; Piper and Fajardo, 2011) and seasonal coupling between supply and demand of carbon for growth (Walter et al., 2005; Smith and Stitt, 2007), are all factors modulating the final carbon balance of tree and their capacity to cope with extreme dry events in the long term (see Sala et al.”
Dynamics of non-structural carbohydrates in terrestrial plants: a global synthesis (2016, background): “On a daily basis, starch storage during the day supplies carbon for growth and respiration at night (Walter et al. 2005, Smith and Stitt 2007).”