including the URL of the record and the reason for the withdrawal request.

Lysenko 91,92 | Armin Macanović 93 | Parastoo Mahdavi 94 | Peter Manning 35 | Corrado Marcenò 13 | Vassiliy Martynenko 95 | Maurizio Mencuccini 96 | Vanessa Minden 97 | Jesper Erenskjold Moeslund 54 | Marco Moretti 98 | Jonas V. Müller 99 | Abstract Aims: Vegetation-plot records provide information on the presence and cover or abundance of plants co-occurring in the same community. Vegetation-plot data are spread across research groups, environmental agencies and biodiversity research centers and, thus, are rarely accessible at continental or global scales. Here we present the sPlot database, which collates vegetation plots worldwide to allow for the exploration of global patterns in taxonomic, functional and phylogenetic diversity at the plant community level.Results: sPlot version 2.1 contains records from 1,121,244 vegetation plots, which comprise 23,586,216 records of plant species and their relative cover or abundance in plots collected worldwide between 1885 and 2015. We complemented the information for each plot by retrieving climate and soil conditions and the biogeographic context (e.g., biomes) from external sources, and by calculating community-weighted means and variances of traits using gap-filled data from the global plant trait database TRY. Moreover, we created a phylogenetic tree for 50,167 out of the 54,519 species identified in the plots. We present the first maps of global patterns of community richness and community-weighted means of key traits. Conclusions: The availability of vegetation plot data in sPlot offers new avenues for vegetation analysis at the global scale. K E Y W O R D S biodiversity, community ecology, ecoinformatics, functional diversity, global scale, macroecology, phylogenetic diversity, plot database, sPlot, taxonomic diversity, vascular plant, vegetation relevé 166 |

The Palaearctic steppes range from the Mediterranean basin towards China, forming one of the largest continuous terrestrial biomes. The literature on steppe ecology and conservation is vast but scattered and often not available in English. We provide a review of some key topics based on a new definition of steppes, which includes also Mediterranean steppes and alpine rangelands of the Asian Highlands. Revisiting the terrestrial ecoregions of the world, we estimate that the Palaearctic steppe biome extends over ca. 10.5 million km 2 . Major chorological regions differ in their macroclimatic niche with a clear distinction between Middle Asia with its winter precipitation and the Central Asian summer-rain regions of the Mongolian plateau and of Tibet. Steppe soils store large amounts of carbon, yet the sequestration potential is debated and depends on land use.

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The stability of ecological communities is critical for the stable provisioning of ecosystem services, such as food and forage production, carbon sequestration, and soil fertility. Greater biodiversity is expected to enhance stability across years by decreasing synchrony among species, but the drivers of stability in nature remain poorly resolved. Our analysis of time series from 79 datasets across the world showed that stability was associated more strongly with the degree of synchrony among dominant species than with species richness. The relatively weak influence of species richness is consistent with theory predicting that the effect of richness on stability weakens when synchrony is higher than expected under random fluctuations, which was the case in most communities. Land management, nutrient addition, and climate change treatments had relatively weak and varying effects on stability, modifying how species richness, synchrony, and stability interact. Our results demonstrate the prevalence of biotic drivers on ecosystem stability, with the potential for environmental drivers to alter the intricate relationship among richness, synchrony, and stability.

Aim To assess the consequences of agricultural intensification since the 1950s for Central Europe's plant communities of arable plants.Location Central Germany.Methods We employed a semipermanent plot design to analyse changes in 392 field interiors for 10 study regions, including sandy, limestone and loamy sites between the 1950s/60s and 2009. ResultsThe analysis revealed a reduction in the regional species pool during the 50-year period of 23% (from 301 to 233 vascular species) and dramatic losses in plot-level diversity (from medians of 24 to 7). Median cover of spontaneously growing arable plants decreased from 30% to 3%. Losses were disproportionally larger on limestone sites while sandy sites maintained a larger fraction of the original diversity. Archaeophytes, neophytes and most Poaceae (including some aggressive weeds) showed similarly strong losses as indigenous plants. This contradicts the assumption that grasses and neophytes are generally profiting from agricultural intensification. Crop diversity decreased from 25 crop plants present in the 1950s/60s to only 16 in 2009, while crop cover generally increased. Winter cereals, oilseed rape and maize are dominant today, while all other crop types showed strong declines.Main conclusions Vegetation change over time depended on soil substrate with once markedly different arable communities now showing more homogenized community structure. Increasing Ellenberg indicator values for nitrogen and pH point to N fertilization as a major driver of change. New conservation measures such as the establishment of field flora reserves and agri-environment schemes with less intensive land use are thus urgently needed especially on limestone substrates to bring an end to the decline of this functionally distinct and increasingly threatened component of the Central European flora.

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With 450,000 kmKobresia (syn. Carex) pygmaea dominated pastures in the eastern Tibetan highlands are the world's largest pastoral alpine ecosystem forming a durable turf cover at 3000-6000 m a.s.l. Kobresia's resilience and competitiveness is based on dwarf habit, predominantly below-ground allocation of photo assimilates, mixture of seed production and clonal growth, and high genetic diversity. Kobresia growth is co-limited by livestock-mediated nutrient withdrawal and, in the drier parts of the plateau, low rainfall during the short and cold growing season. Overstocking has caused pasture degradation and soil deterioration over most parts of the Tibetan highlands and is the basis for this man-made ecosystem. Natural autocyclic processes of turf destruction and soil erosion are initiated through polygonal turf cover cracking, and accelerated by soil-dwelling endemic small mammals in the absence of predators. The major consequences of vegetation cover deterioration include the release of large amounts of C, earlier diurnal formation of clouds, and decreased surface temperatures. These effects decrease the recovery potential of Kobresia pastures and make them more vulnerable to anthropogenic pressure and climate change. Traditional migratory rangeland management was sustainable over millennia, and possibly still offers the best strategy to conserve and possibly increase C stocks in the Kobresia turf.