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Root system architecture is a fundamentally important trait for resource acquisition in both ecological and agronomic contexts.
Resource acquisition in herbivores can be optimised through the modulation of their intake and patch selection, both being strongly dependent on the characteristics of swards.
Our experimental design allowed us to disentangle the independent effects of juvenile resource acquisition in both sexes (as reflected by body size) and resource acquisition by adult males (feeding).
Dissecting how much of the differences between the populations are due to the effects of dietary intake versus genetic divergence will shed light on the important role of resource acquisition in the evolution of nuptial feeding mating systems and the adaptive plasticity of life-history trade-offs in general.
According to classic theoretical predictions on resource acquisition in animals, individuals should be distributed in environments so as to maximise their fitness.
For instance, many laboratory studies have addressed the importance of genetic variation in resource acquisition in driving positive relationships between suites of life-history traits (King et al.
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A schematic representation of the hypothesis that V36 females allocated resources to functions related to the rapid change in priority between litters, rather than to increasing resource acquisition, is in Figure 6 (reprinted from Pascual et al. [ 18]).
We show that under certain conditions, root modification in the presence of a secondary species may limit competition as tree-crop root plasticity differentiates belowground allocation and resource acquisition zones in an agroforestry system.
Neither the different foundational criteria of LP and V females (i.e. LP vs. V36) nor the selection history of line V (i.e. V16 vs. V36) altered the females' resource acquisition capacity in normal conditions.
For example, multiple matings could have facilitated resource acquisition, either in direct exchange for sex (Symons, 1979) or by eliciting paternal investment from multiple men via paternity confusion (Hrdy, 1981).
This preference is thought to reflect the direct benefits of large body size in territory defense, resource acquisition, and reproduction in addition to genetic benefits associated with mating with a large-bodied partner.
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