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A four-compartment lettuce model designed to predict the effects of abrupt changes in nitrogen availability is described.
Our simulations help to interpret and understand responses of plant metabolism, which include rearrangements of metabolic fluxes and changes in energy and reductant requirements, as a result of changes in nitrogen availability.
Traditional bottom culture Gracilaria farms face production problems mainly related to the cultivation system and seasonal changes in nitrogen availability and irradiance.
Yet, our understanding of the responses of long-lived species such as trees to changes in nitrogen availability is based primarily on studies of the growth response of individual trees or seedlings and saplings to experimental changes in nitrogen availability [3], [4], [5] that are scaled-up to the population level [6].
Our finding that secondary succession occurred independently of changes in nitrogen availability supports the findings of Menge et al. [22] that forest ecosystems are not limited by available nitrogen over long time scales.
It is clear that diverse strategies to respond to changes in nitrogen availability have evolved in the prokaryote kingdom.
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In a previous QTL study, we have demonstrated that a simple change in nitrogen availability completely changes the genetic control of biomass growth and allocation, as well as carbon partitioning within wood components [ 62].
Assuming crop husbandry factors are unchanged, farm yields would show only marginal increases (3 6%) due to climate change owing to limitations in nitrogen availability.
We noted that the 'nitrogen metabolism' pathway was directly involved in nitrogen availability [ 26].
Glucose uptake in E. coli is regulated in response to perturbations in nitrogen availability.
The rapamycin-sensitive TORC1 complex, universally conserved among eukaryotic cells, is the central mediator and coordinator of physiological responses of the cell to changes in nitrogen source and availability (De Virgilio and Loewith 2006a).
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