Add to ORKGEvolutionary theory for life-history allometry in mammals is extended to include a trade-off between body-size growth rate and adult lifespan
Background: To maximize their fitness, parents are assumed to allocate their resources optimally bet...
Several phenomenological descriptions, such as the von Bertalanffy growth model, have been widely us...
AbstractSeveral phenomenological descriptions, such as the von Bertalanffy growth model, have been w...
Size dependence of mortality over the ontogeny is added to life-history optimization schemes for ma...
Evolutionary theory for life-history allometry in mammals is extended to include a trade-off between...
If we assume that adult life span and age-at-maturity are described correctly by quarter power allom...
Optimization models have been widely and successfully used in evolutionary ecology to predict the at...
This article develops a new evolutionary model for life histories by combining a new production-grow...
The recently formulated metabolic theory of ecology has profound implications for the evolution of l...
A unified approach is developed for the evolutionary structure of mammalian life histories; it blend...
The Smith-Fretwell model for optimal offspring size assumes the existence of an inverse proportional...
<p>The pace of life history is highly variable across mammals, and several evolutionary biologists h...
Understanding evolutionary coordination among different life‐history traits is a key challenge for e...
The Smith‐Fretwell model for optimal offspring size assumes the existence of an inverse proportional...
It is suggested that Damuth’s ‘energy-equivalence rule’ for mammal populations follows from a partic...
Background: To maximize their fitness, parents are assumed to allocate their resources optimally bet...
Several phenomenological descriptions, such as the von Bertalanffy growth model, have been widely us...
AbstractSeveral phenomenological descriptions, such as the von Bertalanffy growth model, have been w...
Size dependence of mortality over the ontogeny is added to life-history optimization schemes for ma...
Evolutionary theory for life-history allometry in mammals is extended to include a trade-off between...
If we assume that adult life span and age-at-maturity are described correctly by quarter power allom...
Optimization models have been widely and successfully used in evolutionary ecology to predict the at...
This article develops a new evolutionary model for life histories by combining a new production-grow...
The recently formulated metabolic theory of ecology has profound implications for the evolution of l...
A unified approach is developed for the evolutionary structure of mammalian life histories; it blend...
The Smith-Fretwell model for optimal offspring size assumes the existence of an inverse proportional...
<p>The pace of life history is highly variable across mammals, and several evolutionary biologists h...
Understanding evolutionary coordination among different life‐history traits is a key challenge for e...
The Smith‐Fretwell model for optimal offspring size assumes the existence of an inverse proportional...
It is suggested that Damuth’s ‘energy-equivalence rule’ for mammal populations follows from a partic...
Background: To maximize their fitness, parents are assumed to allocate their resources optimally bet...
Several phenomenological descriptions, such as the von Bertalanffy growth model, have been widely us...
AbstractSeveral phenomenological descriptions, such as the von Bertalanffy growth model, have been w...