Sea-age variation in maiden Atlantic salmon spawners: phenotypic plasticity or genetic polymorphism?

Atlantic salmon exhibit a partially heritable polymorphism in which the morphs are distinguished by the duration and location of the sea-phase of their life-cycle. These morphs co-occur, albeit in characteristically different proportions, in most Scottish rivers and in both the spring and autumn spawner runs; early running fish being generally associated with upland spawning locations while late running fish are associated with lowland spawning. Thus, differences in riverine and marine environment appear to be linked to differences in the relative abundance of the morphs, rather than to the specific morph which is optimally adapted.

Stochastic growth reduces population fluctuations in Daphnia-algal systems.

Deterministic, size-structured models are widely used to describe consumer-resource interactions. Such models typically ignore potentially large random variability in juvenile development rates. We present simple representations of this variability and show five approaches to calculating the model parameters for Daphnia pulex interacting with its algal food.

Maturity dispersion, stock auto-correlation, and management strategy in exploited populations.

Fishery management policies need to be based on historical summaries of stock status which are well correlated with the size of the group of individuals who will be affected by any harvest. This paper is motivated by the problem of managing stocks of Atlantic salmon, which can be accurately monitored during the riverine stages of their life-history, but which spend a lengthy period at sea before returning to spawn. We begin by formulating a minimal stochastic model of stock-recruitment driven population dynamics, which linearises to a standard ARMA form.

The dynamics of size-at-age variability.

In this paper, we propose a theoretical framework within which a unified treatment of the key sources of size-at-age variability-size dependence of growth rate, stochastic growth rate variations and individual-to-individual variability in growth performance-is possible. We use this framework to develop a general criterion for growth depensation in cohorts, which we define as the increase of the coefficient of variation of size-at-age, with increasing age. We use this criterion to show that size dependence of growth rate, acting alone, is depensatory only if the growth rate increases faster than linearly with size (that is, if growth is faster than exponential), while stochastic growth rate variation is invariably depensatory.

Modeling the demographic effects of endocrine disruptors.

In this article we describe a series of strategic models of populations and individuals subject to challenge by endocrine disruptors. These models are not designed to be fitted to detailed data on specific species but rather are intended to provide general insights on the relative importance of different demographic mechanisms in the population context. Therefore, the models contain the minimum necessary biological detail, but in recompense they are highly accessible to mathematical analysis.

Resource allocation, hyperphagia and compensatory growth.

Organisms often shown enhanced growth during recovery from starvation, and can even overtake continuously fed conspecifics (overcompensation). In an earlier paper (Ecology 84, 2777-2787), we studied the relative role played by hyperphagia and resource allocation in producing overcompensation in juvenile (non-reproductive) animals. We found that, although hyperphagia always produces growth compensation, overcompensation additionally requires protein allocation control which routes assimilate preferentially to structure during recovery.