2,777 research outputs found

    Mimicry - Sheep in wolves' clothing

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    A framework for modelling and analysing conspecific brood parasitism

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    Recently several papers that model parasitic egg-laying by birds in the nests of others of their own species have been published. Whilst these papers are concerned with answering different questions, they approach the problem in a similar way and have a lot of common features. In this paper a framework is developed which unifies these models, in the sense that they all become special cases of a more general model. This is useful for two main reasons; firstly in order to aid clarity, in that the assumptions and conclusions of each of the models are easier to compare. Secondly it provides a base for further similar models to start from. The basic assumptions for this framework are outlined and a method for finding the ESSs of such models is introduced. Some mathematical results for the general, and more specific, models are considered and their implications discussed. In addition we explore the biological consequences of the results that we have obtained and suggest possible questions which could be investigated using models within or very closely related to our framework

    Does practice shape the brain?

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    Combining motility and bioluminescent signalling aids mate finding in deep-sea fish: a simulation study

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    We present a model to estimate the mean time required for mate finding among deep-sea fish as a function of motility and the extent of bioluminescent signalling. This model differs from those of previous works in 3 important ways by including (1) sex differences in motility, (2) a maximum detection range of bioluminescent signals derived from a recently published mechanistic model based on physical principles and the physiology of vision, and (3) a novel consideration of the likelihood of individuals passing within detection range only in the interval between flashes and hence, failing to detect the signaller. We argue that the flash rates required for effective detection are low, with rates of less than 1 per minute being entirely plausible, and that predation pressure may further encourage low flash rates. Further, even at high flash frequencies, the energetic cost of bioluminescent signalling is argued to be a trivial fraction of resting metabolic rates. Using empirically derived estimates for parameter values, we estimate that a female will be detected and reached by a male within 2 to 4 h of beginning to signal. Hence, we argue that mate finding may not seriously restrict reproductive success in species that can exploit this signalling system. We further argue that where male motility allows bioluminescent signalling, this may have some advantages over chemical-based signalling. Bioluminescent signalling may, therefore, be more important to mate finding in the deep sea (relative to chemical signals) than some previous works have suggested

    An evolutionarily stable joining policy for group foragers

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    For foragers that exploit patchily distributed resources that are challenging to locate, detecting discoveries made by others with a view to joining them and sharing the patch may often be an attractive tactic, and such behavior has been observed across many taxa. If, as will commonly be true, the time taken to join another individual on a patch increases with the distance to that patch, then we would expect foragers to be selective in accepting joining opportunities: preferentially joining nearby discoveries. If competition occurs on patches, then the profitability of joining (and of not joining) will be influenced by the strategies adopted by others. Here we present a series of models designed to illuminate the evolutionarily stable joining strategy. We confirm rigorously the previous suggestion that there should be a critical joining distance, with all joining opportunities within that distance being accepted and all others being declined. Further, we predict that this distance should be unaffected by the total availability of food in the environment, but should increase with decreasing density of other foragers, increasing speed of movement towards joining opportunities, increased difficulty in finding undiscovered food patches, and decreasing speed with which discovered patches can be harvested. We are further able to make predictions as to how fully discovered patches should be exploited before being abandoned as unprofitable, with discovered patches being more heavily exploited when patches are hard to find: patches can be searched for remaining food more quickly, forager density is low, and foragers are relatively slow in traveling to discovered patches

    Professor W. E. Ayrton, 1847-1908: the \u27Never-resting, Keen-eyed chief\u27

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    Volume â…£, Part 3: Engineers & teachers in Meiji Japan, Chapter 1

    John Newman (1925-1993): Judoka, Broadcaster and Academic

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    Volume X, Chapter 1

    Consequences of variation in predator attack for the evolution of the selfish herd

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    There is a strong body of evidence that patterns of collective behaviour in grouping animals are governed by interactions between small numbers of individuals within the group. These findings contrast with study of the ‘selfish herd’, where increasingly complex individual-level movement rules have been proposed to explain the rapid increase in aggregation observed when prey groups are startled by or detect a predator. While individuals using simple rules take into account the position of only a few neighbours, those using complex rules incorporate multiple neighbours, and their relative distance, to determine their movement direction. Here, we simulate the evolution of selfish herd behaviour to assess the conditions under which simple and complex movement rules might evolve, explicitly testing predictions arising from previous work. We find that complex rules outperform simple ones under a range of predator attack strategies, but that simple rules can fix in populations particularly when they are already in the majority, suggesting strong positive frequency dependence in rule success. In addition, we explore whether a movement rule derived from studies of collective behaviour (where individuals use the position of seven neighbours to determine movement direction) performs as successfully as more complex rules, finding again positive frequency dependence in rule success, and a particular role for predator attack strategy (from within or outside the group)

    Professor W. E. Ayrton, 1847-1908: the \u27Never-resting, Keen-eyed chief\u27 - Notes

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    Volume â…£, Part 3: Engineers & teachers in Meiji Japan, Chapter 15, Note
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