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Fawcett, T. W.

Publications and source records attributed to Fawcett, T. W..

3 recordsLinked to original sources

Acorn-omics: Optimal Foraging Behaviour Generates Steep Discounting and Preference Reversals in Laboratory Tasks

Classic foraging models and discounting tasks may oversimplify the decision-makers environment, resulting in a discrepancy between predicted and observed behaviour. In delay discounting tasks, animals typically steeply devalue larger-later (LL) outcomes, choosing smaller-sooner (SS) rewards after short delays. This steep discounting appears to be irreconcilable with natural foraging behaviour, where animals frequently endure long delays when travelling to find food, handling tough items, and storing food for future use. This apparent mismatch in behaviour has led to questions regarding the ecological validity of laboratory discounting tasks. Here, we developed a rich dynamic optimisation model to identify the conditions under which animals should choose LL or SS outcomes. In our model, a food-storing animal encounters food items differing in energy content and handling time and must decide which items to eat immediately and which to cache, so that it has enough stored food to survive winter. We simulated a range of environments, including laboratory conditions where foragers face negligible predation risk when searching for food and have a high probability of finding food, compared to more natural conditions where searching for food is risky, and food is harder to find. In line with preference reversals seen in the discounting literature, our model predicts that LL items should be rejected more often when the handling time for such items is increased, whereas SS items should be rejected more often when the handling time for both items is increased. Importantly, our model only predicts rejection of food items under parameter values that reflect laboratory conditions, supporting the notion that the steep devaluation of rewards seen in animals may be driven by the artificiality of traditional discounting tasks.

animal behavior and cognition↗

Biomimetic robots reveal flexible adjustment of sexual signalling in a wild invertebrate.

Sexual signals are often structured in bouts, which can be adjusted in response to changes in the signallers physical and social environment. For example, we might expect individuals to adjust their own signalling behaviour in response to changes in the signalling behaviour of rivals, because this can affect their relative attractiveness to potential mates. In this study, we used a biomimetic robot to experimentally manipulate rival waving behaviour in a wild population of fiddler crabs (Afruca tangeri), and investigated whether this leads to changes in the activity and waving behaviour of a focal male. Analysing the focal males behaviour using hidden Markov models and linear hurdle models, we found no evidence that the focal males waving rate changed in response to changes in the behaviour of the robotic rival. However, bouts of waving lasted longer when the robotic rival was waving at a fast rate. Focal males were also less likely to enter their burrow when the robotic rival was waving, and spent less time in their burrow if they did enter. These results reveal tactical adjustment of behaviour by competing signallers, and highlight the flexible nature of bout-structured sexual displays.

animal behavior and cognition↗

The evolution of dynamic and flexible courtship displays that reveal individual quality

Sexual selection is a major force shaping morphological and behavioral diversity. Existing theory focuses on courtship display traits such as morphological ornaments whose costs and benefits are assumed be to fixed across individuals lifetimes. In contrast, empirically observed displays are often inherently dynamic, as vividly illustrated by the acrobatic dances, loud vocalizations, and vigorous motor displays involved in courtship behavior across a broad range of taxa. One empirically observed form of display flexibility occurs when signalers adjust their courtship investment based on the number of rival signalers. The predictions of established sexual selection theory cannot readily be extended to such displays because display expression varies between courtship events, such that any given display may not reliably reflect signaler quality. Thus, we lack an understanding of how dynamic displays coevolve with sexual preferences and how signalers should tactically adjust their display investment across multiple courtship opportunities. To address these questions, we extended an established model of the coevolution of a female sexual preference and a male display trait to allow for dynamic, flexible displays. We find that a dynamic display can coevolve with a sexual preference away from their naturally selected optima, though display intensity is a weaker signal of male quality than for static ornaments. Furthermore, we find that males evolve to decrease their display investment when displaying alongside more rivals. This research represents a first step towards generalizing the findings of sexual selection theory to account for the ubiquitous dynamism of animal courtship. Significance StatementAnimal courtship displays are typically costly for survival: songs attract predators; dances are exhausting; extravagant plumage is cumbersome. Because of the trade-off between mating benefits and survival costs, displaying individuals often vary their displays across time, courting more intensely when the potential benefit is higher or the cost is lower. Despite the ubiquity of such adjustment in nature, existing theory cannot account for how this flexibility might affect the coevolution of displays with sexual preferences, nor for the patterns of tactical display adjustment that might result, because those models treat displays as static, with fixed costs and benefits. Generalizing a well-studied model of sexual selection, we find that a static display and a flexible display can evolve under similar conditions. Our model predicts that courtship should be less intense when more competitors are present.

evolutionary biology↗