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Nature | 2000

Global patterns in biodiversity

Kevin J. Gaston

To a first approximation, the distribution of biodiversity across the Earth can be described in terms of a relatively small number of broad-scale spatial patterns. Although these patterns are increasingly well documented, understanding why they exist constitutes one of the most significant intellectual challenges to ecologists and biogeographers. Theory is, however, developing rapidly, improving in its internal consistency, and more readily subjected to empirical challenge.


(2007) | 2000

Pattern and process in macroecology

Kevin J. Gaston; Tim M. Blackburn

© 2000 by Blackwell Science Ltd. All rights reserved. Issues of scale have become increasingly important to ecologists. This book addresses the structure of regional (large-scale) ecological assemblages or communities, and the influence this has at a local (small-scale) level. This macroecological perspective is essential for the broader study of ecology because the structure and function of local communities cannot be properly understood without reference to the region in which they are situated. The book reviews and synthesizes the issues of current importance in macroecology, providing a balanced summary of the field that will be useful for biologists at advanced undergraduate level and above. These general issues are illustrated by frequent reference to specific well-studied local and regional assemblages -- an approach that serves to relate the macroecological perspective (which is perhaps often difficult to comprehend) to the everyday experience of local sites. Macroecology is an expanding and dynamic discipline. The broad aim of the book is to promote an understanding of why it is such an important part of the wider program of research into ecology. Summarises the current macroecological literature. Provides numerous examples of key patterns. Explicitly links local and regional scale processes. Exploits detailed knowledge of one species assemblage to explore broad issues in the structuring of biodiversity.


Nature | 2004

Effectiveness of the global protected area network in representing species diversity

Ana S. L. Rodrigues; Sandy Andelman; Mohamed I. Bakarr; Luigi Boitani; Thomas M. Brooks; Richard M. Cowling; Lincoln D. C. Fishpool; Gustavo A. B. da Fonseca; Kevin J. Gaston; Michael R. Hoffmann; Janice S. Long; Pablo A. Marquet; John D. Pilgrim; Robert L. Pressey; Jan Schipper; Wes Sechrest; Simon N. Stuart; Les G. Underhill; Robert W. Waller; Matthew E. Watts; Xie Emily Yan

The Fifth World Parks Congress in Durban, South Africa, announced in September 2003 that the global network of protected areas now covers 11.5% of the planets land surface. This surpasses the 10% target proposed a decade earlier, at the Caracas Congress, for 9 out of 14 major terrestrial biomes. Such uniform targets based on percentage of area have become deeply embedded into national and international conservation planning. Although politically expedient, the scientific basis and conservation value of these targets have been questioned. In practice, however, little is known of how to set appropriate targets, or of the extent to which the current global protected area network fulfils its goal of protecting biodiversity. Here, we combine five global data sets on the distribution of species and protected areas to provide the first global gap analysis assessing the effectiveness of protected areas in representing species diversity. We show that the global network is far from complete, and demonstrate the inadequacy of uniform—that is, ‘one size fits all’—conservation targets.


Nature | 2005

Global hotspots of species richness are not congruent with endemism or threat

C. David L. Orme; Richard G. Davies; Malcolm D. Burgess; Felix Eigenbrod; Nicola Pickup; Valerie A. Olson; Andrea J. Webster; Tzung-Su Ding; Pamela C. Rasmussen; Robert S. Ridgely; Ali J. Stattersfield; Peter M. Bennett; Tim M. Blackburn; Kevin J. Gaston; Ian P. F. Owens

Biodiversity hotspots have a prominent role in conservation biology, but it remains controversial to what extent different types of hotspot are congruent. Previous studies were unable to provide a general answer because they used a single biodiversity index, were geographically restricted, compared areas of unequal size or did not quantitatively compare hotspot types. Here we use a new global database on the breeding distribution of all known extant bird species to test for congruence across three types of hotspot. We demonstrate that hotspots of species richness, threat and endemism do not show the same geographical distribution. Only 2.5% of hotspot areas are common to all three aspects of diversity, with over 80% of hotspots being idiosyncratic. More generally, there is a surprisingly low overall congruence of biodiversity indices, with any one index explaining less than 24% of variation in the other indices. These results suggest that, even within a single taxonomic class, different mechanisms are responsible for the origin and maintenance of different aspects of diversity. Consequently, the different types of hotspots also vary greatly in their utility as conservation tools.


Conservation Biology | 2008

Quantification of Extinction Risk: IUCN's System for Classifying Threatened Species

Georgina M. Mace; Nigel J. Collar; Kevin J. Gaston; Craig Hilton-Taylor; H. Resit Akçakaya; Nigel Leader-Williams; E. J. Milner-Gulland; Simon N. Stuart

The International Union for Conservation of Nature (IUCN) Red List of Threatened Species was increasingly used during the 1980s to assess the conservation status of species for policy and planning purposes. This use stimulated the development of a new set of quantitative criteria for listing species in the categories of threat: critically endangered, endangered, and vulnerable. These criteria, which were intended to be applicable to all species except microorganisms, were part of a broader system for classifying threatened species and were fully implemented by IUCN in 2000. The system and the criteria have been widely used by conservation practitioners and scientists and now underpin one indicator being used to assess the Convention on Biological Diversity 2010 biodiversity target. We describe the process and the technical background to the IUCN Red List system. The criteria refer to fundamental biological processes underlying population decline and extinction. But given major differences between species, the threatening processes affecting them, and the paucity of knowledge relating to most species, the IUCN system had to be both broad and flexible to be applicable to the majority of described species. The system was designed to measure the symptoms of extinction risk, and uses 5 independent criteria relating to aspects of population loss and decline of range size. A species is assigned to a threat category if it meets the quantitative threshold for at least one criterion. The criteria and the accompanying rules and guidelines used by IUCN are intended to increase the consistency, transparency, and validity of its categorization system, but it necessitates some compromises that affect the applicability of the system and the species lists that result. In particular, choices were made over the assessment of uncertainty, poorly known species, depleted species, population decline, restricted ranges, and rarity; all of these affect the way red lists should be viewed and used. Processes related to priority setting and the development of national red lists need to take account of some assumptions in the formulation of the criteria.


Proceedings of the Royal Society of London. Series B, Biological Sciences | 2000

Thermal tolerance, climatic variability and latitude

Abraham Addo-Bediako; Steven L. Chown; Kevin J. Gaston

The greater latitudinal extents of occurrence of species towards higher latitudes has been attributed to the broadening of physiological tolerances with latitude as a result of increases in climatic variation. While there is some support for such patterns in climate, the physiological tolerances of species across large latitudinal gradients have seldom been assessed. Here we report findings for insects based on published upper and lower lethal temperature data. The upper thermal limits show little geographical variation. In contrast, the lower bounds of supercooling points and lower lethal temperatures do indeed decline with latitude. However, this is not the case for the upper bounds, leading to an increase in the variation in lower lethal limits with latitude. These results provide some support for the physiological tolerance assumption associated with Rapoports rule, but highlight the need for coupled data on species tolerances and range size.


Biology Letters | 2007

Psychological benefits of greenspace increase with biodiversity.

Richard A. Fuller; Katherine N. Irvine; Patrick Devine-Wright; Philip H. Warren; Kevin J. Gaston

The worlds human population is becoming concentrated into cities, giving rise to concerns that it is becoming increasingly isolated from nature. Urban public greenspaces form the arena of many peoples daily contact with nature and such contact has measurable physical and psychological benefits. Here we show that these psychological benefits increase with the species richness of urban greenspaces. Moreover, we demonstrate that greenspace users can more or less accurately perceive species richness depending on the taxonomic group in question. These results indicate that successful management of urban greenspaces should emphasize biological complexity to enhance human well-being in addition to biodiversity conservation.


Biological Reviews | 2005

Species-energy relationships at the macroecological scale: a review of the mechanisms

Karl L. Evans; Philip H. Warren; Kevin J. Gaston

Correlations between the amount of energy received by an assemblage and the number of species that it contains are very general, and at the macro‐scale such species‐energy relationships typically follow a monotonically increasing curve. Whilst the ecological literature contains frequent reports of such relationships, debate on their causal mechanisms is limited and typically focuses on the role of energy availability in controlling the number of individuals in an assemblage. Assemblages from high‐energy areas may contain more individuals enabling species to maintain larger, more viable populations, whose lower extinction risk elevates species richness. Other mechanisms have, however, also been suggested. Here we identify and clarify nine principal mechanisms that may generate positive species‐energy relationships at the macro‐scale. We critically assess their assumptions and applicability over a range of spatial scales, derive predictions for each and assess the evidence that supports or refutes them. Our synthesis demonstrates that all mechanisms share at least one of their predictions with an alternative mechanism. Some previous studies of species‐energy relationships appear not to have recognised the extent of shared predictions, and this may detract from their contribution to the debate on causal mechanisms. The combination of predictions and assumptions made by each mechanism is, however, unique, suggesting that, in principle, conclusive tests are possible. Sufficient testing of all mechanisms has yet to be conducted, and no single mechanism currently has unequivocal support. Each may contribute to species‐energy relationships in some circumstances, but some mechanisms are unlikely to act simultaneously. Moreover, a limited number appear particularly likely to contribute frequently to species‐energy relationships at the macro‐scale. The increased population size, niche position and diversification rate mechanisms are particularly noteworthy in this context.


Journal of Animal Ecology | 1997

Interspecific abundance-range size relationships: An appraisal of mechanisms

Kevin J. Gaston; Tim M. Blackburn; John H. Lawton

1. Positive relationships between the local abundance and the range size of the species in a taxonomic assemblage are very general. 2. Explanations for these relationships typically focus on two mechanisms, based on differences in the niche breadths of species, or metapopulation dynamics. Others have, however, also been suggested. 3. Here we identify and clarify all the principal mechanisms proposed to explain positive interspecific abundance-range size relationships. We critically assess the assumptions and predictions that they make, and the evidence in support of them. 4. A number of predictions are common to all of the biological (as opposed to artefactual) mechanisms, but the combination of predictions and assumptions made by each is unique, suggesting that, in principle, conclusive tests of all of the mechanisms are possible. 5. On present evidence, no single mechanism has unequivocal support. We discuss reasons why this might be the case.


Journal of Applied Ecology | 1996

Biodiversity : a biology of numbers and difference

Kevin J. Gaston

What is biodiversity? Part 1 Measuring biodiversity: genetics of biological diversity - from varieties to species comparing character diversity among biotas species richness - measure and measurement measuring relations among biodiversity, ecological function and functional diversity diversity and higher-levels of organization. Part 2 Patterns in biodiversity: spatial and temporal patterns of genetic diversity within species spatial patterns in taxonomic diversity temporal changes in biodiversity - detecting patterns and identifying causes spatial and temporal patterns in functional diversity. Part 3 Conservation and management: does biodiversity matter? - evaluating the case for conserving species identifying priorities for the conservation of biodiversity - systematic biological criteria within a socio-political framework managing biodiversity biodiversity and global change.

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