6 research outputs found

    The relationship between the functional diversity, functional redundancy and community stability in mountain rangelands

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    Aims We studied species redundancy, functional redundancy, and community stability relationship in mountain rangelands of Northern Iran via assessing vegetation and soil resources. This study aimed to examine whether community redundancy contributes to community stability, quantify the importance of species redundancy versus functional redundancy to keep the stability of the community, and compare the relationship between these community and altitude gradient. Methods Ecological gradient determined by its environment, and disturbance factors were used to evaluate the variation in diversity, redundancy, and stability across a range of communities. We constructed a structural equation model (SEM) based on the bivariate relationships to understand the causal pathways through which the species diversity indices, functional diversity, redundancy diversity, and soil nutrients affect community stability. Results Positive and significant path coefficients were found for functional diversity and redundancy, species redundancy, and altitude gradient with stability. There was a significantly negative effect of functional diversity on species diversity. Species function had no effect on species redundancy. Conclusions Community stability improved at higher functional redundancy. In general, it can be concluded that the math- ematical representation of functional redundancy can be an effective tool to evaluate the causal models which link plant diversity to community stability

    Grazing intensity alters the plant diversity‐ecosystem carbon storage relationship in rangelands across topographic and climatic gradients

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    1. Plant diversity supports multiple ecosystem functions, including carbon sequestration. Recent shifts in plant diversity in rangelands due to increased grazing pressure and climate changes have the potential to impact the sequestration of carbon in arid to semi-humid regions worldwide. However, plant diversity, grazing intensity and carbon storage are also influenced by environmental factors such as nutrient availability, climate, and topography. The complexity of these interactions limits our ability to fully assess the impacts of grazing on biodiversity-ecosystem function (BEF) relationships. Read the free Plain Language Summary for this article on the Journal blog. 2. We assessed how grazing intensity modifies BEF relationships by determining the links between plant diversity and ecosystem carbon stocks (plant and soil carbon) across broad environmental gradients and different plant growth forms. To achieve this, we surveyed 1493 quadrats across 10 rangelands, covering an area of 23,756 ha in northern Iran. 3. We show that aboveground carbon stocks increased with plant diversity across topographic, climatic and soil fertility gradients. The relationship between aboveground carbon stocks and plant diversity was strongest for forbs, followed by shrubs and grasses. Soil carbon stocks increased strongly with soil fertility across sites, but aridity, grazing, plant diversity and topography were also important in explaining variation in soil carbon stocks. 4. Importantly, aboveground and soil carbon stocks declined at high grazing intensity, and grazing modified the relationship between plant diversity and carbon stocks regardless of differences in abiotic conditions across sites. 4. Our study demonstrates that relationships between plant diversity and ecosystem carbon stocks persist across gradients of aridity, topography, and soil fertility, but the relationships are modified by grazing intensity. Our findings suggest that potential losses in plant diversity under grazing intensification could reduce ecosystem carbon storage across wide areas of arid to semi-humid rangelands. We discuss the potential mechanisms underpinning rangeland BEF relationships to stimulate future research

    Benchmarking plant diversity of Palaearctic grasslands and other open habitats

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    Aims Understanding fine-grain diversity patterns across large spatial extents is fundamental for macroecological research and biodiversity conservation. Using the GrassPlot database, we provide benchmarks of fine-grain richness values of Palaearctic open habitats for vascular plants, bryophytes, lichens and complete vegetation (i.e., the sum of the former three groups). Location Palaearctic biogeographic realm. Methods We used 126,524 plots of eight standard grain sizes from the GrassPlot database: 0.0001, 0.001, 0.01, 0.1, 1, 10, 100 and 1,000 m2 and calculated the mean richness and standard deviations, as well as maximum, minimum, median, and first and third quartiles for each combination of grain size, taxonomic group, biome, region, vegetation type and phytosociological class. Results Patterns of plant diversity in vegetation types and biomes differ across grain sizes and taxonomic groups. Overall, secondary (mostly semi-natural) grasslands and natural grasslands are the richest vegetation type. The open-access file ”GrassPlot Diversity Benchmarks” and the web tool “GrassPlot Diversity Explorer” are now available online (https://edgg.org/databases/GrasslandDiversityExplorer) and provide more insights into species richness patterns in the Palaearctic open habitats. Conclusions The GrassPlot Diversity Benchmarks provide high-quality data on species richness in open habitat types across the Palaearctic. These benchmark data can be used in vegetation ecology, macroecology, biodiversity conservation and data quality checking. While the amount of data in the underlying GrassPlot database and their spatial coverage are smaller than in other extensive vegetation-plot databases, species recordings in GrassPlot are on average more complete, making it a valuable complementary data source in macroecology

    Benchmarking plant diversity of Palaearctic grasslands and other open habitats

    No full text
    Aims: Understanding fine-grain diversity patterns across large spatial extents is fundamental for macroecological research and biodiversity conservation. Using the GrassPlot database, we provide benchmarks of fine-grain richness values of Palaearctic open habitats for vascular plants, bryophytes, lichens and complete vegetation (i.e., the sum of the former three groups). Location: Palaearctic biogeographic realm. Methods: We used 126,524 plots of eight standard grain sizes from the GrassPlot database: 0.0001, 0.001, 0.01, 0.1, 1, 10, 100 and 1,000 m(2) and calculated the mean richness and standard deviations, as well as maximum, minimum, median, and first and third quartiles for each combination of grain size, taxonomic group, biome, region, vegetation type and phytosociological class. Results: Patterns of plant diversity in vegetation types and biomes differ across grain sizes and taxonomic groups. Overall, secondary (mostly semi-natural) grasslands and natural grasslands are the richest vegetation type. The open-access file "GrassPlot Diversity Benchmarks" and the web tool "GrassPlot Diversity Explorer" are now available online () and provide more insights into species richness patterns in the Palaearctic open habitats. Conclusions: The GrassPlot Diversity Benchmarks provide high-quality data on species richness in open habitat types across the Palaearctic. These benchmark data can be used in vegetation ecology, macroecology, biodiversity conservation and data quality checking. While the amount of data in the underlying GrassPlot database and their spatial coverage are smaller than in other extensive vegetation-plot databases, species recordings in GrassPlot are on average more complete, making it a valuable complementary data source in macroecology

    Benchmarking plant diversity of Palaearctic grasslands and other open habitats

    No full text
    Abstract Aims: Understanding fine-grain diversity patterns across large spatial extents is fundamental for macroecological research and biodiversity conservation. Using the GrassPlot database, we provide benchmarks of fine-grain richness values of Palaearctic open habitats for vascular plants, bryophytes, lichens and complete vegetation (i.e., the sum of the former three groups). Location: Palaearctic biogeographic realm. Methods: We used 126,524 plots of eight standard grain sizes from the GrassPlot database: 0.0001, 0.001, 0.01, 0.1, 1, 10, 100 and 1,000 m² and calculated the mean richness and standard deviations, as well as maximum, minimum, median, and first and third quartiles for each combination of grain size, taxonomic group, biome, region, vegetation type and phytosociological class. Results: Patterns of plant diversity in vegetation types and biomes differ across grain sizes and taxonomic groups. Overall, secondary (mostly semi-natural) grasslands and natural grasslands are the richest vegetation type. The open-access file ”GrassPlot Diversity Benchmarks” and the web tool “GrassPlot Diversity Explorer” are now available online (https://edgg.org/databases/GrasslandDiversityExplorer) and provide more insights into species richness patterns in the Palaearctic open habitats. Conclusions: The GrassPlot Diversity Benchmarks provide high-quality data on species richness in open habitat types across the Palaearctic. These benchmark data can be used in vegetation ecology, macroecology, biodiversity conservation and data quality checking. While the amount of data in the underlying GrassPlot database and their spatial coverage are smaller than in other extensive vegetation-plot databases, species recordings in GrassPlot are on average more complete, making it a valuable complementary data source in macroecology
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