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Mires or peatlands host unique biodiversity and provide many valuable ecosystem services. Mires often undergo different development phases during their evolution. Two mire phases that have clearly divergent hydrological regimes and characteristic biotas are minerotrophic fen and ombrotrophic bog. Open mires can be overgrown by trees and develop into peatland forests. Mire development trajectories are expected to be associated with three major factors—post‐glacial isostatic uplift, autogenic succession and climate‐induced changes. Understanding long‐term mire development is important for the conservation planning of these threatened habitats.We use data from modern pollen samples to characterize differences between the pollen signal and to identify indicator pollen taxa for three mire development phases—open fens, forested fens and bogs. The modern reference samples are then used to support the interpretation of the sediment records in terms of mire development phases and related biodiversity changes in six mires within a 20 × 30 km area in western Saaremaa, Estonia. Palynological richness and phylogenetic diversity (PD) as well as Ellenberg indicator values are compared throughout the 10,000‐year history of the Saaremaa mires.Pollen of herbaceous taxa discriminates between open fens, forested fens and bogs, and indicator pollen taxa can be associated with each mire phase. In general, the fen phases of the mires show higher richness and PD than the bog phases but there is considerable variation between the sites. The mire diversity peaks are often associated with transitional periods when high local community heterogeneity allows the coexistence of high numbers of taxa from different phylogenetic lineages.Synthesis. When the initiation of mires in isostatic land uplift areas is closely related to water‐level changes and the position of the sites in relation to the sea, the development of mires and their biodiversity in the late Holocene is associated with local conditions but mediated by climate. The ongoing rapid climate change is likely to accelerate changes in existing mires, and while the transitional periods are characterized by high diversity, these periods are temporary, and the overall diversity of mires can be expected to decrease. [ABSTRACT FROM AUTHOR]

Global change drivers (e.g. climate and land use) affect the species and functional traits observed in a local site but also its dark diversity—the set of species and traits locally suitable but absent. Dark diversity links regional and local scales and, over time, reveals taxa under expansion lags by depicting the potential biodiversity that remains suitable but is absent locally. Since global change effects on biodiversity are both spatially and temporally scale dependent, examining long-term temporal dynamics in observed and dark diversity would be relevant to assessing and foreseeing biodiversity change. Here, we used sedimentary pollen data to examine how both taxonomic and functional observed and dark diversity changed over the past 14 500 years in northern Europe. We found that taxonomic and functional observed and dark diversity increased over time, especially after the Late Glacial and during the Late Holocene. However, dark diversity dynamics revealed expansion lags related to species' functional characteristics (dispersal limitation and stress intolerance) and an extensive functional redundancy when compared to taxa in observed diversity. We highlight that assessing observed and dark diversity dynamics is a promising tool to examine biodiversity change across spatial scales, its possible causes, and functional consequences. [ABSTRACT FROM AUTHOR]

European dry thin-soil calcareous grasslands (alvars) are species-rich semi-natural habitats. Cessation of traditional management, such as mowing and grazing, leads to shrub and tree encroachment and the local extinction of characteristic alvar species. While soil microbes are known to play a critical role in driving vegetation and ecosystem dynamics, more information is needed about their composition and function in grasslands of different dynamic stages. Here we assess the composition of soil fungal, prokaryotic, and plant communities using soil environmental DNA from restored alvar grasslands in Estonia. The study areas included grasslands that had experienced different degrees of woody encroachment prior to restoration (woody plant removal and grazing), as well as unmanaged open grasslands. We found that, in general, different taxonomic groups exhibited correlated patterns of between-community variation. Previous forest sites, which had prior to restoration experienced a high degree of woody encroachment by ectomycorrhizal Scots pine, were compositionally most distinct from managed open grasslands, which had little woody vegetation even prior to restoration. The functional structure of plant and fungal communities varied in ways that were consistent with the representation of mycorrhizal types in the ecosystems prior to restoration. Compositional differences between managed and unmanaged open grasslands reflecting the implementation of grazing without further management interventions were clearer among fungal, and to an extent prokaryotic, communities than among plant communities. While previous studies have shown that during woody encroachment of alvar grassland, plant communities change first and fungal communities follow, our DNA-based results suggest that microbial communities reacted faster than plant communities during the restoration of grazing management in alvar grassland. We conclude that while the plant community responds faster to cessation of management, the fungal community responds faster to restoration of management. This may indicate hysteresis, where the eventual pathway back to the original state (grazed ecosystem) differs from the pathway taken towards the alternative state (abandoned semi-natural grassland ecosystem). [ABSTRACT FROM AUTHOR]

Research over the past decade has shown that quantifying spatial variation in ecosystem properties is an effective approach to investigating the effects of environmental change on ecosystems. Yet, current consensus among scientists is that we need a better understanding of short‐ and long‐term (temporal) variation in ecosystem properties to plan effective ecosystem management and predict future ecologies.Trait‐based approaches can be used to reconstruct ecosystem properties from long‐term ecological records and contribute significantly to developing understandings of ecosystem change over decadal to millennial time‐scales.Here, we synthesise current trait‐based approaches and explore how organisms' functional traits (FTs) can be scaled across time and space. We propose a framework for reconstructing long‐term variation in ecosystems by means of analysing FTs derived from palaeoecological datasets. We then summarise challenges that must be overcome to reconcile trait‐based approaches with palaeo‐datasets. Finally, we discuss the benefits and limitations of trait‐based reconstructions of ecosystem temporal dynamics and suggest future directions for research.Reconstructing environmental properties through time vis‐à‐vis FTs can be separated into two parts. The first is to record trait data for organisms present in modern ecosystems, and the second is to reconstruct temporal variability in FTs from palaeoecological datasets, capturing changes in trait composition over time. Translating palaeoecological datasets into FTs is challenging due to taphonomic, taxonomic and chronological uncertainties, as well as uniformitarian assumptions. Explicitly identifying and addressing these challenges is important to effectively calculate changes in FT through time.Palaeo‐trait research offers insights into questions related to short‐ and long‐term ecosystem functioning, environmental change and extinction and community assembly rules across time. As work in this area matures, we expect that trait‐based approaches integrating palaeoecology and neo‐ecology will improve understanding of past ecologies and provide a deeper insight of their implications for present‐day and future ecosystem management and conservation. Read the free Plain Language Summary for this article on the Journal blog. [ABSTRACT FROM AUTHOR]

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/datab ases/Grass landD ivers ityEx plorer) 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. [ABSTRACT FROM AUTHOR]