139 research outputs found

    Beta-diversity of Central European forests decreases along an elevational gradient due to the variation in local community assembly processes

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    Beta-diversity has been repeatedly shown to decline with increasing elevation, but the causes of this pattern remain unclear, partly because they are confounded by coincident variation in alpha- and gamma-diversity. We used 8,795 forest vegetation-plot records from the Czech National Phytosociological Database to compare the observed patterns of beta diversity to null-model expectations (beta-deviation) controlling for the effects of alpha- and gamma-diversity. We tested whether \b{eta}-diversity patterns along a 1,200 m elevation gradient exclusively depend on the effect of varying species pool size, or also on the variation of the magnitude of community assembly mechanisms determining the distribution of species across communities (e.g., environmental filtering, dispersal limitation). The null model we used is a novel extension of an existing null-model designed for presence/absence data and was specifically designed to disrupt the effect of community assembly mechanisms, while retaining some key features of observed communities such as average species richness and species abundance distribution. Analyses were replicated in ten subregions with comparable elevation ranges. Beta-diversity declined along the elevation gradient due to a decrease in gamma-diversity, which was steeper than the decrease in alpha-diversity. This pattern persisted after controlling for alpha- and gamma-diversity variation, and the results were robust when different resampling schemes and diversity metrics were used. We conclude that in temperate forests the pattern of decreasing beta-diversity with elevation does not exclusively depend on variation in species pool size, as has been hypothesized, but also on variation in community assembly mechanisms. The results were consistent across resampling schemes and diversity measures, thus supporting the use of vegetation plot databases for understanding...Comment: Accepted version 25 pages, 5 figures, 1 tabl

    Forest management plans as data source for the assessment of the conservation status of European Union habitat types

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    Natura 2000 is a European network of protected sites that should enable natural habitats to be maintained or restored at a favorable conservation status. Progress toward this objective must be periodically reported by states members of the European Union. We investigated how forest management plans might provide data to support the reporting. The study was done in the forests of the Dolomites and Venetian Prealps, Italy. Here, about 200 forest management plans, divided into several forest compartments, have been drawn up and revised every 10–15 years. Stand structure variables were retrieved from past (OR, 1970–1980) and more recent revisions (NR, 2000–2010) of 331 forest compartments ranging between 0.35 and 53.1 ha. In the beech and spruce forest habitat types (coded 9130 and 9410 in Annex I of the Directive 92/43/EEC, respectively), we found an increase from OR to NR in the density of large trees (from 32 to 46/ha and from 31 to 50/ha, respectively for the two habitats), basal area (from 27.3 to 31.5 m2/ha and from 31 to 34.5 m2/ha), mean diameter (from 34.1 to 36.2 cm and from 33.9 to 36 cm) and Gini index (from 0.35 to 0.37 and from 0.33 to 0.36). Pursuant to the Directive 92/43/EEC, the conservation status of these two habitat types should be taken as “favorable” with regards to the criterion related to the habitats’ specific structure and functions that are necessary for its long-term maintenance. We conclude that forest management plans provide a great portion of the information needed for assessing and monitoring the conservation status of forest habitat types in the Natura 2000 framework

    GrassPlot v. 2.00 : first update on the database of multi-scale plant diversity in Palaearctic grasslands

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    GrassPlot is a collaborative vegetation-plot database organised by the Eurasian Dry Grassland Group (EDGG) and listed in the Global Index of Vegetation-Plot Databases (GIVD ID EU-00-003). Following a previous Long Database Report (Dengler et al. 2018, Phyto-coenologia 48, 331–347), we provide here the first update on content and functionality of GrassPlot. The current version (GrassPlot v. 2.00) contains a total of 190,673 plots of different grain sizes across 28,171 independent plots, with 4,654 nested-plot series including at least four grain sizes. The database has improved its content as well as its functionality, including addition and harmonization of header data (land use, information on nestedness, structure and ecology) and preparation of species composition data. Currently, GrassPlot data are intensively used for broad-scale analyses of different aspects of alpha and beta diversity in grassland ecosystems

    Quantifying the effect of sampling plot size on the estimation of structural indicators in old-growth forest stands

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    There is increasing awareness that structure-based indicators should be considered for assessing the biological value of late successional forests. In order to increase the unique habitat features critical for old-growth associated species, it is important to identify and rank candidate potential forest sites on the basis of their distinctive structural features. Data on living and deadwood components for the identification of old-growth condition are usually acquired in the considered forest stands by two sampling survey: (i) census performed in relatively large monitoring sites; (ii) network of small sampling units, on which inventory practices are usually based. Several authors argued that choosing between these survey strategies might have substantial effects on the values of common indicators of old-growth condition. Our study aims at (i) assessing the total estimate differences among old-growth structural indicators measured in field plots with different sizes, and (ii) defining the optimal sample size for the reliable assessment of such indicators. The study was carried out in six beech dominated forest stands on the Apennines range in Italy. In each stand, living and deadwood components were surveyed and geocoded in 1-ha square areas. Based on these dataset, circular plots with radii ranging from 4 m up to 20 m were then considered in order to quantify the effect of sampling plot size on the estimation of four structural indicators: (1) number of living trees; (2) number of large trees (dbhP50 cm); (3) total deadwood volume; (4) number of deadwood elements (snags, dead standing trees; lying dead trees, lying deadwood)with dbh (or average diameter for lying deadwood)P30 cm. We found that the size of the sampling plots should be at least 500 m2 in order to establish a database for the assessment of the investigated indicators. The census approach should be preferred to the sampling plot approach for old-growth forest stands smaller than 3–5 ha. The achieved results contribute to define assessment protocols for characterizing and ranking the degree to which forest stands approximate old-growth condition based on standardized indicators.L'articolo è disponibile sul sito dell'editore www.elsevier.com/locate/forec

    Protection gaps and restoration opportunities for primary forests in Europe

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    Aims: Primary forests are critical for forest biodiversity and provide key ecosystem services. In Europe, these forests are particularly scarce and it is unclear whether they are sufficiently protected. Here we aim to: (a) understand whether extant primary forests are representative of the range of naturally occurring forest types, (b) identify forest types which host enough primary forest under strict protection to meet conservation targets and (c) highlight areas where restoration is needed and feasible. Location: Europe. Methods: We combined a unique geodatabase of primary forests with maps of forest cover, potential natural vegetation, biogeographic regions and protected areas to quantify the proportion of extant primary forest across Europe\u27s forest types and to identify gaps in protection. Using spatial predictions of primary forest locations to account for underreporting of primary forests, we then highlighted areas where restoration could complement protection. Results: We found a substantial bias in primary forest distribution across forest types. Of the 54 forest types we assessed, six had no primary forest at all, and in two-thirds of forest types, less than 1% of forest was primary. Even if generally protected, only ten forest types had more than half of their primary forests strictly protected. Protecting all documented primary forests requires expanding the protected area networks by 1,132 km2 (19,194 km2 when including also predicted primary forests). Encouragingly, large areas of non-primary forest existed inside protected areas for most types, thus presenting restoration opportunities. Main conclusion: Europe\u27s primary forests are in a perilous state, as also acknowledged by EU\u27s “Biodiversity Strategy for 2030.” Yet, there are considerable opportunities for ensuring better protection and restoring primary forest structure, composition and functioning, at least partially. We advocate integrated policy reforms that explicitly account for the irreplaceable nature of primary forests and ramp up protection and restoration efforts alike

    GrassPlot v. 2.00 – first update on the database of multi-scale plant diversity in Palaearctic grasslands

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    Abstract: GrassPlot is a collaborative vegetation-plot database organised by the Eurasian Dry Grassland Group (EDGG) and listed in the Global Index of Vegetation-Plot Databases (GIVD ID EU-00-003). Following a previous Long Database Report (Dengler et al. 2018, Phyto- coenologia 48, 331–347), we provide here the first update on content and functionality of GrassPlot. The current version (GrassPlot v. 2.00) contains a total of 190,673 plots of different grain sizes across 28,171 independent plots, with 4,654 nested-plot series including at least four grain sizes. The database has improved its content as well as its functionality, including addition and harmonization of header data (land use, information on nestedness, structure and ecology) and preparation of species composition data. Currently, GrassPlot data are intensively used for broad-scale analyses of different aspects of alpha and beta diversity in grassland ecosystems
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