Biomedical subjects

Andrew R Watkinson

Publications and source records attributed to Andrew R Watkinson.

6 recordsLinked to original sources

PubMed2006

Opposing forces of aerosol cooling and El Nino drive coral bleaching on Caribbean reefs.

Bleaching of corals as a result of elevated sea surface temperatures (SST) is rapidly becoming a primary source of stress for reefs globally; the scale and extent of this threat will depend on how the drivers of SST interact to influence bleaching patterns. We demonstrate how the opposing forces of the El Niño-Southern Oscillation (ENSO) and levels of atmospheric aerosols drive regional-scale patterns of coral bleaching across the Caribbean. When aerosol levels are low, bleaching is largely determined by El Niño strength, but high aerosol levels mitigate the effects of a severe El Niño. High aerosol levels, resulting principally from recent volcanic activity, have thus protected Caribbean reefs from more frequent widespread bleaching events but cannot be relied on to provide similar protection in the future.

Aerosols↗

PubMed2006

Census error and the detection of density dependence.

1. Studies aiming to identify the prevalence and nature of density dependence in ecological populations have often used statistical analysis of ecological time-series of population counts. Such time-series are also being used increasingly to parameterize models that may be used in population management. 2. If time-series contain measurement errors, tests that rely on detecting a negative relationship between log population change and population size are biased and prone to spuriously detecting density dependence (Type I error). This is because the measurement error in density for a given year appears in the corresponding change in population density, with equal magnitude but opposite sign. 3. This effect introduces bias that may invalidate comparisons of ecological data with density-independent time-series. Unless census error can be accounted for, time-series may appear to show strongly density-dependent dynamics, even though the density-dependent signal may in reality be weak or absent. 4. We distinguish two forms of census error, both of which have serious consequences for detecting density dependence. 5. First, estimates of population density are based rarely on exact counts, but on samples. Hence there exists sampling error, with the level of error depending on the method employed and the number of replicates on which the population estimate is based. 6. Secondly, the group of organisms measured is often not a truly self-contained population, but part of a wider ecological population, defined in terms of location or behaviour. Consequently, the subpopulation studied may effectively be a sample of the population and spurious density dependence may be detected in the dynamics of a single subpopulation. In this case, density dependence is detected erroneously, even if numbers within the subpopulation are censused without sampling error. 7. In order to illustrate how process variation and measurement error may be distinguished we review data sets (counts of numbers of birds by single observers) for which both census error and long-term variance in population density can be estimated. 8. Tests for density dependence need to obviate the problem that measured population sizes are typically estimates rather than exact counts. It is possible that in some cases it may be possible to test for density dependence in the presence of unknown levels of census error, for example by uncovering nonlinearities in the density response. However, it seems likely that these may lack power compared with analyses that are able to explicitly include census error and we review some recently developed methods.

Animals↗

PubMed2005

Characterising spatial and temporal variation in the finite rate of population increase across the northern range boundary of the annual grass Vulpia fasciculata.

Understanding the factors that influence plant distributions is a considerable challenge for ecologists in the face of environmental change. Here, we quantify spatial and temporal variation in the finite rate of population increase of the annual grass Vulpia fasciculata. Specifically, we test the hypothesis that the northern range boundary is associated with finite rates of population increase of less than one. Seeds of three ecotypes of the annual grass V. fasciculata were introduced annually across a range of sites in Great Britain both within (11) and to the north (4) of its current range boundary in each of 4 years. Populations failed to establish at 17% of target sites due to disturbance. At the remaining target sites, the finite rate of population increase, lambda, varied from 0.06 to 33.3 with a geometric mean of 1.88. Of the total variance in the rate of population growth, site and year effects accounted independently for 40% of the variation and in interaction for 50%; ecotype accounted for less than 5% of the variation. Variation in the weather between sites and years had little impact on plant performance, and there was no indication that the rate of population growth was lower to the north of the current range boundary. We conclude that current climatic conditions on the coast of Great Britain are not limiting the distribution of V. fasciculata and that seeds from across its current range have roughly equivalent colonising potential.

Analysis of Variance↗

PubMed2003

Demographic threats to the sustainability of Brazil nut exploitation.

A comparative analysis of 23 populations of the Brazil nut tree (Bertholletia excelsa) across the Brazilian, Peruvian, and Bolivian Amazon shows that the history and intensity of Brazil nut exploitation are major determinants of population size structure. Populations subjected to persistent levels of harvest lack juvenile trees less than 60 centimeters in diameter at breast height; only populations with a history of either light or recent exploitation contain large numbers of juvenile trees. A harvesting model confirms that intensive exploitation levels over the past century are such that juvenile recruitment is insufficient to maintain populations over the long term. Without management, intensively harvested populations will succumb to a process of senescence and demographic collapse, threatening this cornerstone of the Amazonian extractive economy.

Bertholletia↗

PubMed2003

The theory and application of plant competition models: an agronomic perspective.

Many studies of plant competition have been directed towards understanding how plants respond to density in monocultures and how the presence of weeds affects yield in crops. In this Botanical Briefing, the development and current understanding of plant competition is reviewed, with particular emphasis being placed on the theory of plant competition and the development and application of mathematical models to crop-weed competition and the dynamics of weeds in crops. By consolidating the results of past research in this manner, it is hoped to offer a context in which researchers can consider the potential directions for future research in competition studies and its application to integrated weed management.

Agriculture↗

PubMed2003

Long-term region-wide declines in Caribbean corals.

We report a massive region-wide decline of corals across the entire Caribbean basin, with the average hard coral cover on reefs being reduced by 80%, from about 50% to 10% cover, in three decades. Our meta-analysis shows that patterns of change in coral cover are variable across time periods but largely consistent across subregions, suggesting that local causes have operated with some degree of synchrony on a region-wide scale. Although the rate of coral loss has slowed in the past decade compared to the 1980s, significant declines are persisting. The ability of Caribbean coral reefs to cope with future local and global environmental change may be irretrievably compromised.

Animals↗