The evolutionary consequences of learning under competition.

Learning is a taxonomically widespread process by which animals change their behavioural responses to stimuli as a result of experience. In this way, it plays a crucial role in the development of individual behaviour and underpins substantial phenotypic variation within populations. Nevertheless, the impact of learning in social contexts on evolutionary change is not well understood.

A critical review of risk-sensitive foraging.

Foraging is risk sensitive if choices depend on the variability of returns from the options as well as their mean return. Risk-sensitive foraging is important in behavioural ecology, psychology and neurophysiology. It has been explained both in terms of mechanisms and in terms of evolutionary advantage.

A general framework for modelling trade-offs in adaptive behaviour.

An animal's behaviour can influence many variables, such as its energy reserves, its risk of injury or mortality, and its rate of reproduction. To identify the optimal action in a given situation, these various effects can be compared in the common currency of reproductive value. While this idea has been widely used to study trade-offs between pairs of variables, e.

Behavioural specialization and learning in social networks.

Interactions in social groups can promote behavioural specialization. One way this can happen is when individuals engage in activities with two behavioural options and learn which option to choose. We analyse interactions in groups where individuals learn from playing games with two actions and negatively frequency-dependent payoffs, such as producer-scrounger, caller-satellite, or hawk-dove games.

Biological adaptation in light of the Lewontin-Williams (a)symmetry.

Neo-Darwinism characterizes biological adaptation as a one-sided process, in which organisms adapt to their environment but not vice versa. This asymmetric relationship-here called Williams' asymmetry-is called into question by Niche Construction Theory, which emphasizes that organisms and their environments often mutually affect each other. Here, we clarify that Williams' asymmetry is specifically concerned with (quasi)-directed modifications toward phenotypes that increase individual fitness.

A critical evaluation of the index of patch quality.

The inverse optimality approach can allow us to learn about an animal's environment by assuming their behaviour is optimal. This approach has been applied to animals diving underwater for food to produce the index of patch quality (IPQ), which aims to provide a proxy for prey abundance or quality in a foraging patch based on the animal's diving behaviour. The IPQ has been used in several empirical studies but has never been evaluated theoretically.

How to Model Optimal Group Size in Social Carnivores.

AbstractModels of optimal group size need to identify the currency that correctly captures the fitness consequences of foraging. Although daily intake or daily net energy gain per animal are widely used as currencies, they are not ideal. They predict that all available time should be spent hunting and do not reflect performance during a hunt.

Matching Behaviours and Rewards.

Matching describes how behaviour is related to rewards. The matching law holds when the ratio of an individual's behaviours equals the ratio of the rewards obtained. From its origins in the study of pigeons working for food in the laboratory, the law has been applied to a range of species, both in the laboratory and outside it (e.

Learning, exploitation and bias in games.

We focus on learning during development in a group of individuals that play a competitive game with each other. The game has two actions and there is negative frequency dependence. We define the distribution of actions by group members to be an equilibrium configuration if no individual can improve its payoff by unilaterally changing its action.

Gains v. losses, or context dependence generated by confusion?

Tversky and Kahneman introduced the term framing for the finding that people give different answers to the same question depending on the way it is posed. One form of framing involves presenting the same outcome as either a gain or a loss. An experiment on starlings by Marsh and Kacelnik suggests that this form of framing occurs in non-humans.

The overall discount rate.

Discounting refers to the way in which the value of an outcome depends on the delay until it is obtained. If an organism's discount function is known, then its rate of discounting at any delay can be found. If the function is not known, the normalised area under an estimate of the discount function has been used as a measure that summarises the strength of discounting over a range of delays.

Mechanistic models must link the field and the lab.

In the theory outlined in the target article, an animal forages continuously, making sequential decisions in a world where the amount of food and its uncertainty are fixed, but delays are variable. These assumptions contrast with the risk-sensitive foraging theory and create a problem for comparing the predictions of this model with many laboratory experiments that do not make these assumptions.

Optimal gut size of small birds and its dependence on environmental and physiological parameters.

Most optimal foraging models assume that the foraging behaviour of small birds depends on a single state variable, their energy reserves in the form of stored fat. Here, we include a second state variable-the contents of the bird's gut-to investigate how a bird should optimise its gut size to minimise its long-term mortality, depending on the availability of food, the size of meal and the bird's digestive constraints. Our results show that (1) the current level of fat is never less important than gut contents in determining the bird's survival; (2) there exists a unique optimal gut size, which is determined by a trade-off between the energetic gains and costs of maintaining a large digestive system; (3) the optimal gut size increases as the bird's digestive cycle becomes slower, allowing the bird to store undigested food; (4) the critical environmental factor for determining the optimal gut size is the mass of food found in a successful foraging effort ("meal size").

Trust your gut: using physiological states as a source of information is almost as effective as optimal Bayesian learning.

Approaches to understanding adaptive behaviour often assume that animals have perfect information about environmental conditions or are capable of sophisticated learning. If such learning abilities are costly, however, natural selection will favour simpler mechanisms for controlling behaviour when faced with uncertain conditions. Here, we show that, in a foraging context, a strategy based only on current energy reserves often performs almost as well as a Bayesian learning strategy that integrates all previous experiences to form an optimal estimate of environmental conditions.

Adaptive and non-adaptive models of depression: A comparison using register data on antidepressant medication during divorce.

Divorce is associated with an increased probability of a depressive episode, but the causation of events remains unclear. Adaptive models of depression propose that depression is a social strategy in part, whereas non-adaptive models tend to propose a diathesis-stress mechanism. We compare an adaptive evolutionary model of depression to three alternative non-adaptive models with respect to their ability to explain the temporal pattern of depression around the time of divorce.

Scalar utility theory and proportional processing: What does it actually imply?

Scalar Utility Theory (SUT) is a model used to predict animal and human choice behaviour in the context of reward amount, delay to reward, and variability in these quantities (risk preferences). This article reviews and extends SUT, deriving novel predictions. We show that, contrary to what has been implied in the literature, (1) SUT can predict both risk averse and risk prone behaviour for both reward amounts and delays to reward depending on experimental parameters, (2) SUT implies violations of several concepts of rational behaviour (e.

Fatness and fitness: exposing the logic of evolutionary explanations for obesity.

To explore the logic of evolutionary explanations of obesity we modelled food consumption in an animal that minimizes mortality (starvation plus predation) by switching between activities that differ in energy gain and predation. We show that if switching does not incur extra predation risk, the animal should have a single threshold level of reserves above which it performs the safe activity and below which it performs the dangerous activity. The value of the threshold is determined by the environmental conditions, implying that animals should have variable 'set points'.

Costs of Foraging Predispose Animals to Obesity-Related Mortality when Food Is Constantly Abundant.

Obesity is an important medical problem affecting humans and animals in the developed world, but the evolutionary origins of the behaviours that cause obesity are poorly understood. The potential role of occasional gluts of food in determining fat-storage strategies for avoiding mortality have been overlooked, even though animals experienced such conditions in the recent evolutionary past and may follow the same strategies in the modern environment. Humans, domestic, and captive animals in the developed world are exposed to a surplus of calorie-rich food, conditions characterised as 'constant-glut'.

Adaptive learning can result in a failure to profit from good conditions: implications for understanding depression.

Background And Objectives: Depression is a major medical problem diagnosed in an increasing proportion of people and for which commonly prescribed psychoactive drugs are frequently ineffective. Development of treatment options may be facilitated by an evolutionary perspective; several adaptive reasons for proneness to depression have been proposed. A common feature of many explanations is that depressive behaviour is a way to avoid costly effort where benefits are small and/or unlikely.

Risk attitudes in a changing environment: An evolutionary model of the fourfold pattern of risk preferences.

A striking feature of human decision making is the fourfold pattern of risk attitudes, involving risk-averse behavior in situations of unlikely losses and likely gains, but risk-seeking behavior in response to likely losses and unlikely gains. Current theories to explain this pattern assume particular psychological processes to reproduce empirical observations, but do not address whether it is adaptive for the decision maker to respond to risk in this way. Here, drawing on insights from behavioral ecology, we build an evolutionary model of risk-sensitive behavior, to investigate whether particular types of environmental conditions could favor a fourfold pattern of risk attitudes.

The starvation-predation trade-off shapes the strategic use of protein for energy during fasting.

The primary function of lipid storage by animals is as an energy source for surviving periods without food. However, muscle and organ protein can be metabolised for energy, and empirical studies have shown that the onset of protein metabolism begins before the exhaustion of lipid reserves. Since protein tissues are important for reasons other than resisting starvation, the adaptive basis for this early onset is unclear.

Capital and income breeding: the role of food supply.

An aspect of life history that has seen increasing attention in recent years is that of strategies for financing the costs of offspring production. These strategies are often described by a continuum ranging from capital breeding, in which costs are met purely from endogenous reserves, to income breeding, in which costs are met purely from concurrent intake. A variety of factors that might drive strategies toward a given point on the capital-income continuum has been reviewed, and assessed using analytical models.

An evolutionary perspective on information processing.

Behavioral ecologists often assume that natural selection will produce organisms that make optimal decisions. In the context of information processing, this means that the behavior of animals will be consistent with models from fields such as signal detection theory and Bayesian decision theory. We discuss work that applies such models to animal behavior and use the case of Bayesian updating to make the distinction between a description of behavior at the level of optimal decisions and a mechanistic account of how decisions are made.

The evolution of decision rules in complex environments.

Models and experiments on adaptive decision-making typically consider highly simplified environments that bear little resemblance to the complex, heterogeneous world in which animals (including humans) have evolved. These studies reveal an array of so-called cognitive biases and puzzling features of behaviour that seem irrational in the specific situation presented to the decision-maker. Here we review an emerging body of work that highlights spatiotemporal heterogeneity and autocorrelation as key properties of most real-world environments that may help us understand why these biases evolved.

On the evolution and optimality of mood States.

Moods can be regarded as fluctuating dispositions to make positive and negative evaluations. Developing an evolutionary approach to mood as an adaptive process, we consider the structure and function of such states in guiding behavioural decisions regarding the acquisition of resources and the avoidance of harm in different circumstances. We use a drift diffusion model of decision making to consider the information required by individuals to optimise decisions between two alternatives, such as whether to approach or withdraw from a stimulus that may be life enhancing or life threatening.