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Peter J. B. Slater

Other affiliations: University of Sussex
Bio: Peter J. B. Slater is an academic researcher from University of St Andrews. The author has contributed to research in topics: Zebra finch & Population. The author has an hindex of 52, co-authored 121 publications receiving 9192 citations. Previous affiliations of Peter J. B. Slater include University of Sussex.


Papers
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Book
30 Oct 2003
TL;DR: The study of bird song focuses on how song develops, sexual selection and female choice, and themes and variations in time and space.
Abstract: Introduction 1. The study of bird song 2. Production and perception 3. How song develops 4. Getting the message across 5. When do birds sing? 6. Recognition and territorial defence 7. Sexual selection and female choice 8. Themes and variations 9. Variation in time and space List of common and scientific names References Index.

2,315 citations

Journal ArticleDOI
TL;DR: It is found that unexpected genetic or environmental factors can have considerable effects on vocal behaviour in birds and mammals and are often more likely to cause changes or differences in vocalizations than investigators may assume.

452 citations

Journal ArticleDOI
TL;DR: Signature whistle copying was rare and did not initiate reunions or specific vocal responses, which strongly support the hypothesis that signature whistles are used to maintain group cohesion.

437 citations

Journal ArticleDOI
14 Nov 2002-Nature
TL;DR: Investigating the response of harbour seals to the underwater calls of different populations of killer whales found that the seals responded strongly to the calls of mammal-eating killer whales and unfamiliar fish- eating killer whales but not to the familiar calls of the local fish-eating population.
Abstract: Predation is a major force in shaping the behaviour of animals, so that precise identification of predators will confer substantial selective advantages on animals that serve as food to others. Because experience with a predator can be lethal, early researchers studying birds suggested that predator recognition does not require learning. However, a predator image that can be modified by learning and experience will be advantageous in situations where cues associated with the predator are highly variable or change over time. In this study, we investigated the response of harbour seals (Phoca vitulina) to the underwater calls of different populations of killer whales (Orcinus orca). We found that the seals responded strongly to the calls of mammal-eating killer whales and unfamiliar fish-eating killer whales but not to the familiar calls of the local fish-eating population. This demonstrates that wild harbour seals are capable of complex acoustic discrimination and that they modify their predator image by selectively habituating to the calls of harmless killer whales. Fear in these animals is therefore focused on local threats by learning and experience.

199 citations


Cited by
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Journal ArticleDOI
TL;DR: A wide variety of data on capacity limits suggesting that the smaller capacity limit in short-term memory tasks is real is brought together and a capacity limit for the focus of attention is proposed.
Abstract: Miller (1956) summarized evidence that people can remember about seven chunks in short-term memory (STM) tasks. How- ever, that number was meant more as a rough estimate and a rhetorical device than as a real capacity limit. Others have since suggested that there is a more precise capacity limit, but that it is only three to five chunks. The present target article brings together a wide vari- ety of data on capacity limits suggesting that the smaller capacity limit is real. Capacity limits will be useful in analyses of information processing only if the boundary conditions for observing them can be carefully described. Four basic conditions in which chunks can be identified and capacity limits can accordingly be observed are: (1) when information overload limits chunks to individual stimulus items, (2) when other steps are taken specifically to block the recoding of stimulus items into larger chunks, (3) in performance discontinuities caused by the capacity limit, and (4) in various indirect effects of the capacity limit. Under these conditions, rehearsal and long-term memory cannot be used to combine stimulus items into chunks of an unknown size; nor can storage mechanisms that are not capacity- limited, such as sensory memory, allow the capacity-limited storage mechanism to be refilled during recall. A single, central capacity limit averaging about four chunks is implicated along with other, noncapacity-limited sources. The pure STM capacity limit expressed in chunks is distinguished from compound STM limits obtained when the number of separately held chunks is unclear. Reasons why pure capacity estimates fall within a narrow range are discussed and a capacity limit for the focus of attention is proposed.

5,677 citations

Journal ArticleDOI
22 Nov 2002-Science
TL;DR: It is argued that an understanding of the faculty of language requires substantial interdisciplinary cooperation and how current developments in linguistics can be profitably wedded to work in evolutionary biology, anthropology, psychology, and neuroscience is suggested.
Abstract: We argue that an understanding of the faculty of language requires substantial interdisciplinary cooperation. We suggest how current developments in linguistics can be profitably wedded to work in evolutionary biology, anthropology, psychology, and neuroscience. We submit that a distinction should be made between the faculty of language in the broad sense (FLB)and in the narrow sense (FLN) . FLB includes a sensory-motor system, a conceptual-intentional system, and the computational mechanisms for recursion, providing the capacity to generate an infinite range of expressions from a finite set of elements. We hypothesize that FLN only includes recursion and is the only uniquely human component of the faculty of language. We further argue that FLN may have evolved for reasons other than language, hence comparative studies might look for evidence of such computations outside of the domain of communication (for example, number, navigation, and social relations).

3,293 citations

Journal Article
TL;DR: In this paper, a test based on two conserved CHD (chromo-helicase-DNA-binding) genes that are located on the avian sex chromosomes of all birds, with the possible exception of the ratites (ostriches, etc.).

2,554 citations

Book ChapterDOI
01 Jan 1998
TL;DR: This chapter discusses Sperm Competition in Birds, Sexual Selection in Spiders and Other Arachnids, and Reproduction, Mating Strategies and Sperm competition in Marsupials and Monotremes.
Abstract: General Themes: G.A. Parker, Sperm Competition and the Evolution of Ejaculates: Towards a Theory Base. A.P. Moller, Sperm Competition and Sexual Selection. W.G. Eberhard, Female Roles in Sperm Competition. J. Wright, Paternity and Paternal Care. Taxonomic Treatments: L.F. Delph and K. Havens, Pollen Competition in Flowering Plants. D.R. Levitan, Sperm Limitation, Gamete Competition and Sexual Selection in External Fertilizers. N.K. Michiels, Mating Conflicts and Sperm Competition in Simultaneous Hermaphrodites. B. Baur, Sperm Competition in Molluscs. M.A. Elgar, Sperm Competition and Sexual Selection in Spiders and Other Arachnids. L.W. Simmons and M.T. Siva-Jothy, Sperm Competition in Insects: Mechanisms and the Potential for Selection. C.W. Petersen and R.R. Warner, Sperm Competition in Fishes. T.R. Halliday, Sperm Competition in Amphibians. M. Olsson and T. Madsen, Sexual Selection and Sperm Competition in Reptiles. T.R. Birkhead, Sperm Competition in Birds: Mechanisms and Function. D.A. Taggart, W.G. Breed, P.D. Temple-Smith, A. Purvis, and G. Shimmin, Reproduction, Mating Strategies and Sperm Competition in Marsupials and Monotremes. M. Gomendio, A.H. Harcourt, and E.R.S. Roldan, Sperm Competition in Mammals. T.R. Birkhead and A.P. Moller, Sperm Competition, Sexual Selection and Different Routes to Fitness. Index.

2,051 citations

Journal ArticleDOI
17 Jun 1999-Nature
TL;DR: It is found that 39 different behaviour patterns, including tool usage, grooming and courtship behaviours, are customary or habitual in some communities but are absent in others where ecological explanations have been discounted.
Abstract: As an increasing number of field studies of chimpanzees (Pan troglodytes) have achieved long-term status across Africa, differences in the behavioural repertoires described have become apparent that suggest there is significant cultural variation1,2,3,4,5,6,7. Here we present a systematic synthesis of this information from the seven most long-term studies, which together have accumulated 151 years of chimpanzee observation. This comprehensive analysis reveals patterns of variation that are far more extensive than have previously been documented for any animal species except humans8,9,10,11. We find that 39 different behaviour patterns, including tool usage, grooming and courtship behaviours, are customary or habitual in some communities but are absent in others where ecological explanations have been discounted. Among mammalian and avian species, cultural variation has previously been identified only for single behaviour patterns, such as the local dialects of song-birds12,13. The extensive, multiple variations now documented for chimpanzees are thus without parallel. Moreover, the combined repertoire of these behaviour patterns in each chimpanzee community is itself highly distinctive, a phenomenon characteristic of human cultures14 but previously unrecognised in non-human species.

1,964 citations