20 research outputs found

    Ecology of bryophytes along altitudinal and latitudinal gradients in New Zealand

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    Six altitudinal transects through temperate rain forests were studied at different latitudes in the South and North Island of New Zealand with respect to species numbers of bryophytes, cover and phytomass of epiphytic bryophytes, composition of life forms and ratio liverworts : mosses. Phytodiversity of bryophytes is almost constant from the lowlands to the high montane belt but decreases in the subalpine belt. Similarly, phytomass and cover increase with elevation but decrease in the subalpine belt. The percentage of liverworts increases accordingly and can reach maxima of 80-90%. The most significant life forms are tails and wefts characteristic for hyperhygric conditions, pendents for cloud belts and cushions for subalpine belts. The altitudinal gradient is much stronger then the latitudinal gradient, that means the differences between the elevations within a transect are more important than the differences between the transects. They are attributed to the humidity. The temperate rain forests of New Zealand have similar bryological characteristics as the tropical rain forests in equatorial latitudes in 2000 – 3000 m altitude but differ in the drier subalpine belt and higher phytomass

    Can we predict which species win when new habitat becomes available?

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    Land cover change is a key component of anthropogenic global environmental change, contributing to changes in environmental conditions of habitats. Deforestation is globally the most widespread and anthropogenically driven land cover change leading to conversion from closed forest to open non-forest habitat. This study investigates the relative roles of geographic features, characteristics of species climatic niche and species traits in determining the ability of open-habitat plant species to take advantage of recently opened habitats. We use current occurrence records of 18 herbaceous, predominantly open-habitat species of the genus Acaena (Rosaceae) to determine their prevalence in recently opened habitat. We tested correlation of species prevalence in anthropogenically opened habitat with (i) geographic features of the spatial distribution of open habitat, (ii) characteristics of species climatic niche, and (iii) species traits related to dispersal. While primary open habitat (naturally open) was characterised by cold climates, secondary open habitat (naturally closed but anthropogenically opened) is characterised by warmer and wetter conditions. We found high levels of variation in the species prevalence in secondary open habitat indicating species differences in their ability to colonise newly opened habitat. For the species investigated, geographical features of habitat and climatic niche factors showed generally stronger relationships with species prevalence in secondary open habitat than functional traits. Therefore, for small herbaceous species, geographical features of habitat and environmental factors appear to be more important than species functional traits for facilitating expansion into secondary open habitats. Our results suggested that the land cover change might have triggered the shifts of factors controlling open-habitat plant distributions from the competition with forest trees to current environmental constraints

    Disentangling the influence of climatic and geological changes on species radiations

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    Aim Our aim was to seek explanations for the differences in the diversity among the austral continents by comparing the diversification rates and patterns in the grass subfamily Danthonioideae. We asked specifically whether diversification is density dependent, whether it is different for each continent, and whether immigration rates impact on diversification rates. We attempted to account for intercontinental differences by comparing the Pleistocene climatic and Neogene geomorphological histories with the inferred diversification rates. Location Mainly the Southern Hemisphere, treated as four areas for the analyses: Africa, Australia, New Zealand and South America. Methods We based our analyses on a densely sampled, dated phylogeny for the grass subfamily Danthonioideae. We compared 24 diversification models for these continental radiations, taking into account speciation models, and extinction and dispersal rates. We used available distribution data to infer the climates under which danthonioids are found, and used these to estimate the change in area and location of suitable habitats between contemporary and Last Glacial Maximum climates. We inferred the geomorphological history from the literature. Results We show that long-distance dispersal led to parallel radiations, which more than doubled the final standing diversity in the subfamily. Diversification models with the strongest support included separate time-varying diversification processes for each major geographical region. Pleistocene climatic fluctuation did not explain the intercontinental differences in diversification patterns. Main conclusions Although our results are consistent with density-dependent diversification, this explanation is not consistent with the time of arrival of danthonioids on each continent. The diversification patterns on the four major Southern Hemisphere landmasses are idiosyncratic. The two most important predictors of diversity may be the lineage-specific effect of time, and the general effect of topographical complexity and orogenesis

    Rapid range shifts of species associated with high levels of climate warming

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    The distributions of many terrestrial organisms are currently shifting in latitude or elevation in response to changing climate. Using a meta-analysis, we estimated that the distributions of species have recently shifted to higher elevations at a median rate of 11.0 meters per decade, and to higher latitudes at a median rate of 16.9 kilometers per decade. These rates are approximately two and three times faster than previously reported. The distances moved by species are greatest in studies showing the highest levels of warming, with average latitudinal shifts being generally sufficient to track temperature changes. However, individual species vary greatly in their rates of change, suggesting that the range shift of each species depends on multiple internal species traits and external drivers of change. Rapid average shifts derive from a wide diversity of responses by individual species

    Direct and indirect effects of climate and habitat factors on butterfly diversity.

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    Many factors, including climate, resource availability, and habitat diversity, have been proposed as determinants of global diversity, but the links among them have rarely been studied. Using structural equation modeling (SEM), we investigated direct and indirect effects of climate variables, host-plant richness, and habitat diversity on butterfly species richness across Britain, at 20-km grid resolution. These factors were all important determinants of butterfly diversity, but their relative contributions differed between habitat generalists and specialists, and whether the effects were direct or indirect. Climate variables had strong effects on habitat generalists, whereas host-plant richness and habitat diversity contributed relatively more for habitat specialists. Considering total effects (direct and indirect together), climate variables had the strongest link to butterfly species richness for all groups of species. The results suggest that different mechanistic hypotheses to explain species richness may be more appropriate for habitat generalists and specialists, with generalists hypothesized to show direct physiological limitations and specialists additionally being constrained by trophic interactions (climate affecting host-plant richness)

    Global biome patterns of the Middle and Late Pleistocene

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    Our primary aim was to assess the hypothesis that distinctive features of the patterns of vegetation change during successive Quaternary glacial–interglacial cycles reflect climatic differences arising from forcing differences. We addressed this hypothesis using 207 half-degree resolution global biome pattern simulations, for time slices between 800 ka and 2 ka, made using the LPJ-GUESS dynamic global vegetation model. Simulations were driven using ice-core atmospheric CO2 concentrations, Earth’s obliquity, and outputs from a pre-industrial and 206 palaeoclimate experiments; four additional simulations were driven using projected future CO2 concentrations. Climate experiments were run using HadCM3. Using a rule-based approach, above-ground biomass and leaf area index of LPJ-GUESS plant functional types were used to infer each grid cell’s biome. The hypothesis is supported by the palaeobiome simulations. To enable comparisons with the climatic forcing, multivariate analyses were performed of global vegetation pattern dissimilarities between simulations. Results showed generally similar responses to glacial–interglacial climatic variations during each cycle, although no two interglacials or glacials had identical biome patterns. Atmospheric CO2 concentration was the strongest driver of the dissimilarity patterns. Dissimilarities relative to the time slice with the lowest atmospheric CO2 concentration show the log–linear relationship to atmospheric CO2 concentration expected of an index of ecocarbon sensitivity. For each simulation, extent and total above-ground biomass of each biome were calculated globally and for three longitudinal segments corresponding to the major continental regions. Mean and minimum past extents of forest biomes, notably Temperate Summergreen Forest, in the three major continental regions strongly parallel relative tree diversities, hence supporting the hypothesis that past biome extents played an important role in determining present diversity. Albeit that they reflect the climatic consequences only of the faster Earth system components, simulated potential future biome patterns are unlike any during the past 800 ky, and likely will continue to change markedly for millennia if projected CO2 concentrations are realised

    The coincidence of climatic and species rarity: high risk to small-range species from climate change

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    Why do areas with high numbers of small-range species occur where they do? We found that, for butterfly and plant species in Europe, and for bird species in the Western Hemisphere, such areas coincide with regions that have rare climates, and are higher and colder areas than surrounding regions. Species with small range sizes also tend to occur in climatically diverse regions, where species are likely to have been buffered from extinction in the past. We suggest that the centres of high small-range species richness we examined predominantly represent interglacial relict areas where cold-adapted species have been able to survive unusually warm periods in the last ca 10 000 years. We show that the rare climates that occur in current centres of species rarity will shrink disproportionately under future climate change, potentially leading to high vulnerability for many of the species they contain

    Projected climatic changes lead to biome changes in areas of previously constant biome

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    Aim Recent studies in southern Africa identified past biome stability as an important predictor of biodiversity. We aimed to assess the extent to which past biome stability predicts present global biodiversity patterns, and the extent to which projected climatic changes may lead to eventual biome changes in areas with constant past biome. Location Global. Taxon Spermatophyta; terrestrial vertebrates. Methods Biome constancy was assessed and mapped using results from 89 dynamic global vegetation model simulations, driven by outputs of palaeoclimate experiments spanning the past 140 ka. We tested the hypothesis that terrestrial vertebrate diversity is predicted by biome constancy. We also simulated potential future vegetation, and hence potential future biome patterns, and quantified and mapped the extent of projected eventual future biome change in areas of past constant biome. Results Approximately 11% of global ice-free land had a constant biome since 140 ka. Apart from areas of constant Desert, many areas with constant biome support high species diversity. All terrestrial vertebrate groups show a strong positive relationship between biome constancy and vertebrate diversity in areas of greater diversity, but no relationship in less diverse areas. Climatic change projected by 2100 commits 46%–66% of global ice-free land, and 34%–52% of areas of past constant biome (excluding areas of constant Desert) to eventual biome change. Main conclusions Past biome stability strongly predicts vertebrate diversity in areas of higher diversity. Future climatic changes will lead to biome changes in many areas of past constant biome, with profound implications for biodiversity conservation. Some projected biome changes will result in substantial reductions in biospheric carbon sequestration and other ecosystem services. SIGNIFICANCE STATEMENT Using global biome patterns inferred from simulations made using the LPJ-GUESS dynamic global vegetation model, we show that a substantial fraction of areas that are simulated to have supported the same biome throughout the last glacial-interglacial cycle are projected to experience biome change as a consequence of 21st century climatic changes. We further show that, with the exception of some desert areas, areas of the highest past biome constancy correspond to areas of the highest terrestrial vertebrate diversity. As a result, the projected biome changes are likely to have disproportionately large negative impacts upon global biodiversity
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