8 research outputs found

    Stipo pulcherrimae-Festucetalia pallentis Pop 1968 of calcareous petrophytic steppes in Ukraine

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    Nine hundred and eight-nine relevés from calcareous petrophytic steppes in Ukraine and its adjacent territories were assessed with the help of expert systems to determine the syntaxonomic affiliation of the plant communities at class and order levels. At least 488 relevés belonging to the class Festuco-Brometea were analyzed using the TWINSPAN algorithm, and 8 distinctive clusters were obtained, recognized as alliances of the order Stipo pulcherrimae-Festucetalia pallentis. A new alliance, Bromopsido cappadocicae-Asphodelinion tauricae, was ascribed to the Crimean Mountains and the presence of two alliances, Diantho lumnitzeri-Seslerion albicantis and Genisto tetragonae-Seselion peucedanifoliae, was confirmed as new for this vegetation in Ukraine. Unlike in the Pannonian Basin, Bromo pannonici-Festucion csikhegyensis alliance communities mentioned in the literature do not occur in Ukraine. Centaureo carbonatae-Koelerion talievii has been provisionally transferred from Festucetalia valesiacae to the order Stipo pulcherrimae-Festucetalia pallentis. Furthermore, we distinguished alliances by their geographic locations and their climatic (thermoregime, cryoregime, light in communities) and edaphic (carbonate content, salinity, and acidity) features

    Phytosociological and ecological peculiarities of Festuca pallens Host in Ukraine

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    This paper is focused on the phytosociological and ecological requirements of the vulnerable species, Festuca pallens, in Ukraine. Based on the analysis of 51 relevés, we recognized the occurrence of Festuca pallens in three associations within the Festuco-Brometea class. Some communities with the presence of Festuca pallens present with transitional stages of succession to forest-edge vegetation according to the expert system refinement. Moreover, we assessed the ecological differences between occupied habitats using Didukh’s phytoindication scales and concluded that the leading ecological factors are soil humidity, nitrogen content, aeration of the soil, salt regime, carbonate content, thermoregime and continentality of the climate. Finally, we evaluated threats to the existence of these communities with the presence of Festuca pallens considering climate change and other impacts of anthropogenic related activities

    Rare shady chasmophytic habitat communities (8210) in Ukraine

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    The characteristics of shadow chasmophytic habitats on shady calcareous rocks in forest conditions are described. For such communities, the forest canopy primarily acts as a shading factor that determines microclimate, humidity and light levels. The characteristic species of the calcareous rock communities are affected by shade and microclimate but are also broadly defined by the properties of the rock type, topography and aspect and are to some extent independent of the development of forest ecosystems. These communities can be found in deciduous forests of the Carpinion betuli, Fagion sylvaticae and Tilio-Acerion alliances, where they are confined to steep calcareous rock faces and cliffs, with a diameter of rocks of more than 2 m. A particular characteristic of these communities is the high abundance of ferns: Asplenium trichomanes, A. ruta-muraria, A. viridis, Phyllitis scolopendrium, Cystopteris fragilis, Polypodium vulgare, a dense cover of bryophytes that occur as mats over rocks, and a low or insignificant contribution of vascular plants. Syntaxonomically, these communities belong to the Polypodietea class (Ctenidio-Polypodietalia vulgaris order, Ctenidio-Polypodion vulgaris alliance) and belong to four informal communities (Isothecium alopecuroides-Polystichum braunii, Porella platyphylla-Asplenium ruta-muraria, Pseudanomodon attenuatus-Chrysosplenium alternifolium and Pedinophyllum interruptum-Polystichum aculeatum). We evaluated indices of environmental parameters according to the synphytoindication method using Didukh’s scales. According to this methodology, an assessment of the threat impacts and indicators of sociological significance shows that the habitat belongs to a rare type (II class), and therefore requires specific conservation measures

    Fine-grain beta diversity of Palaearctic grassland vegetation

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    Questions: Which environmental factors influence fine-grain beta diversity of vegetation and do they vary among taxonomic groups? Location: Palaearctic biogeographic realm. Methods: We extracted 4,654 nested-plot series with at least four different grain sizes between 0.0001 m² and 1,024 m² from the GrassPlot database, covering a wide range of different grassland and other open habitat types. We derived extensive environmental and structural information for these series. For each series and four taxonomic groups (vascular plants, bryophytes, lichens, all), we calculated the slope parameter (z-value) of the power law species–area relationship (SAR), as a beta diversity measure. We tested whether z-values differed among taxonomic groups and with respect to biogeographic gradients (latitude, elevation, macroclimate), ecological (site) characteristics (several stress–productivity, disturbance and heterogeneity measures, including land use) and alpha diversity (c-value of the power law SAR). Results: Mean z-values were highest for lichens, intermediate for vascular plants and lowest for bryophytes. Bivariate regressions of z-values against environmental variables had rather low predictive power (mean R² = 0.07 for vascular plants, less for other taxa). For vascular plants, the strongest predictors of z-values were herb layer cover (negative), elevation (positive), rock and stone cover (positive) and the c-value (U-shaped). All tested metrics related to land use (fertilization, livestock grazing, mowing, burning, decrease in naturalness) led to a decrease in z-values. Other predictors had little or no impact on z-values. The patterns for bryophytes, lichens and all taxa combined were similar but weaker than those for vascular plants. Conclusions: We conclude that productivity has negative and heterogeneity positive effects on z-values, while the effect of disturbance varies depending on type and intensity. These patterns and the differences among taxonomic groups can be explained via the effects of these drivers on the mean occupancy of species, which is mathematically linked to beta diversity

    Fine‐grain beta diversity of Palaearctic grassland vegetation

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    Questions Which environmental factors influence fine-grain beta diversity of vegetation and do they vary among taxonomic groups? Location Palaearctic biogeographic realm. Methods We extracted 4,654 nested-plot series with at least four different grain sizes between 0.0001 m2 and 1,024 m2 from the GrassPlot database, covering a wide range of different grassland and other open habitat types. We derived extensive environmental and structural information for these series. For each series and four taxonomic groups (vascular plants, bryophytes, lichens, all), we calculated the slope parameter (z-value) of the power-law species–area relationship (SAR), as a beta diversity measure. We tested whether z-values differed among taxonomic groups and with respect to biogeographic gradients (latitude, elevation, macroclimate), ecological (site) characteristics (several stress-productivity, disturbance and heterogeneity measures, including land use) and alpha diversity (c-value of the power-law SAR). Results Mean z-values were highest for lichens, intermediate for vascular plants and lowest for bryophytes. Bivariate regressions of z-values against environmental variables had rather low predictive power (mean R2 = 0.07 for vascular plants, less for other taxa). For vascular plants, the strongest predictors of z-values were herb layer cover (negative), elevation (positive), rock and stone cover (positive) and the c-value (u-shaped). All tested metrics related to land use (fertilisation, livestock grazing, mowing, burning, decrease in naturalness) led to a decrease in z-values. Other predictors had little or no impact on z-values. The patterns for bryophytes, lichens and all taxa combined were similar but weaker than those for vascular plants. Main conclusions We conclude that productivity has negative and heterogeneity positive effects on z-values, while the effect of disturbance varies depending on type and intensity. These patterns and the differences among taxonomic groups can be explained via the effects of these drivers on the mean occupancy of species, which is mathematically linked to beta diversity

    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 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
    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
    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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