Marion Island (47°S, 38°E) has one of the most oceanic climates on earth, with consistently low air temperatures, high precipitation, constantly high humidity, and low incident radiation. Since 1968 mean surface air temperature has increased significantly, by 0.025° C year. This was strongly associated with corresponding changes in sea surface temperature but only weakly, or not at all, with variations in radiation and precipitation. We suggest that changing sealevel (atmospheric and oceanic) circulation patterns in the region underlie all of these changes. Sub-Antarctic terrestrial ecosystems are characterized by being species-poor and having a simple trophic structure. Marion Island is no exception and a scenario is presented of the implications of climatic change for the structure and functioning of its ecosystem. Primary production on the island is high and consequently the vegetation has a large annual requirement for nutrients. There are no macroherbivores and even the insects play only a small role as herbivores, so most of the energy and nutrients incorporated in primary production go through a detritus, rather than grazing, cycle. Ameliorating temperatures and increasing CO levels are expected to increase productivity and nutrient demand even further. However, most of the plant communities occur on soils which have especially low available levels of nutrients and nutrient mineralization from organic reserves is the main bottleneck in nutrient cycling and primary production. Increasing temperatures will not significantly enhance microbially-mediated mineralization rates since soil microbiological processes on the island are strongly limited by waterlogging, rather than by temperature. The island supports large numbers of soil macro-arthropods, which are responsible for most of the nutrient release from peat and litter. The activities of these animals are strongly temperature dependent and increasing temperature will result in enhanced nutrient availability, allowing the potential for increased primary production due to elevated temperature and CO levels to be realized. However, housemice occur on the island and have an important influence on the ecosystem, mainly by feeding on soil invertebrates. The mouse population is strongly temperature-limited and appears to be increasing, possibly as a result of ameliorating temperatures. We suggest that an increasing mouse population, through enhanced predation pressure on soil invertebrates, will decrease overall rates of nutrient cycling and cause imbalances between primary production and decomposition. This, along with more direct effects of mice (e.g. granivory) has important implications for vegetation succession and ecosystem structure and functioning on the island. Some of these are already apparent from comparisons with nearby Prince Edward Island where mice do not occur. Other implications of climatic change for the island are presented which emphasize the very marked influences that invasive organisms have on ecosystem structure and functioning. We sugges...
Abstract. Soil chemistry and vegetation data for 176 sites on sub‐Antarctic Marion Island (47° S, 38° E) were subjected to Canonical Correspondence Analysis. 21 habitats in six habitat complexes were recognized from a clustering analysis of the site scores on the canonical axes. Another two habitats and one habitat complex were added to this. The resultant habitat classification closely reflects the between‐habitat variation in the relative magnitudes of the main forcing variables that determine ecological succession on the island (moisture, exposure, parent soil material, salt‐spray and manuring and trampling by seals and seabirds). It can be used by persons with a minimum of botanical or soil expertise. The habitat complexes (number of habitats in complex) are: Coastal Salt‐spray Complex (2); Fellfield (2); Slope (6); Biotic Grassland (3); Biotic Herbfield (3); Mire (6); Polar Desert (1). A key is provided whereby the habitat to which a particular site belongs can be determined using botanical criteria, although infrequently soil moisture and pH information is also needed. Summaries of the soil chemistry and vegetation characteristics of the various habitats are also provided.
The densities, diets and habitat preferences of the soil macrofaunal species on sub-Antarctic Marion Island (47°S, 38°E) are described. Their role in N cycling on the island is assessed, using a mire-grassland community as an example. Primary production on the island is high and this leads to a substantial annual requirement of nutrients by the vegetation. This requirement must almost wholly be met by mineralization of nutrient reserves in the organic matter. Rates of peat nitrogen mineralization mediated by microorganisms alone are much too low to account for rates of N uptake by the vegetation. Although soil macroinvertebrates, and bacteria represent a very small fraction of the total N pool, their interaction accounts for most of the peat N mineralization, as indicated by the amounts of inorganic N released into solution in microcosms. Extrapolation of the microcosm results shows that the soil macrofauna (mainly earthworms) stimulate the release of enough N from the mire-grassland peat to account for maximum N mineralization rates calculated from temporal changes in peat inorganic N levels and plant uptake during the most active part of the growing season. Considering that large numbers of mesoand microinvertebrates occur and must also contribute to nutrient mineralization, the soil faunal component is clearly of crucial importance to nutrient cycling on Marion Island. This is probably true of all sub-Antarctic islands.
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