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Deciduous forests form the dominant natural vegetation of Europe today, but were restricted to small refugia during Pleistocene cold stages, implying an evolutionary past shaped by recurrent range contractions and expansions. Cold‐stage forest refugia were probably widespread in southern and central Europe, with the northwestern Balkan Peninsula being of particular importance. However, the actual number and location of deciduous forest refugia, as well as the connections between them, remain disputed. Here, we address the evolutionary dynamics of the deciduous forest understorey species Euphorbia carniolica as a proxy for past forest dynamics. To do so, we obtained genomic and morphometric data from populations representing the species' entire range, investigated phylogenetic position and intraspecific genetic variation, tested explicit demographic scenarios and applied species distribution models. Our data support two disjoint groups linked to separate refugia on the northwestern and central Balkan Peninsula. We find that genetic differentiation between groups started in the early Pleistocene via vicariance, suggesting a larger distribution in the past. Both refugia acted as sources for founder events to the southeastern Alps and the Carpathians; the latter were likely colonised before the last cold stage. In line with traditional views on the pre‐Pleistocene origin of many southeastern European deciduous forest species, the origin of E. carniolica was dated to the late Pliocene. The fact that E. carniolica evolved at a time when a period of continuous forestation was ending in much of Eurasia provides an interesting biogeographical perspective on the past links between Eurasian deciduous forests and their biota. [ABSTRACT FROM AUTHOR]

Aim: Our knowledge of Pleistocene refugia and post‐glacial recolonization routes of forest understorey plants is still very limited. The geographical ranges of these species are often rather narrow and show highly idiosyncratic, often fragmented patterns indicating either narrow and species‐specific ecological tolerances or strong dispersal limitations. However, the relative roles of these factors are inherently difficult to disentangle. Location: Central and south‐eastern Europe. Time period: 17,100 BP – present. Major taxa studied: Five understorey herbs of European beech forests: Aposeris foetida, Cardamine trifolia, Euphorbia carniolica, Hacquetia epipactis and Helleborus niger. Methods: We used spatio‐temporally explicit modelling to reconstruct the post‐glacial range dynamics of the five forest understorey herbs. We varied niche requirements, demographic rates and dispersal abilities across plausible ranges and simulated the spread of species from potential Pleistocene refugia identified by phylogeographical analyses. Then we identified the parameter settings allowing for the most accurate reconstruction of their current geographical ranges. Results: We found a largely homogenous pattern of optimal parameter settings among species. Broad ecological niches had to be combined with very low but non‐zero rates of long‐distance dispersal via chance events and low rates of seed dispersal over moderate distances by standard dispersal vectors. However, long‐distance dispersal events, although rare, led to high variation among replicated simulation runs. Main conclusions: Small and fragmented ranges of many forest understorey species are best explained by a combination of broad ecological niches and rare medium‐ and long‐distance dispersal events. Stochasticity is thus an important determinant of current species ranges, explaining the idiosyncratic distribution patterns of the study species despite strong similarities in refugia, ecological tolerances and dispersal abilities. [ABSTRACT FROM AUTHOR]

Aims: Oak–hornbeam forests and related vegetation types (phytosociological order Carpinetalia betuli) are widespread in temperate western Eurasia. However, their national classification systems are poorly compatible, and a broad‐scale classification based on numerical analyses is lacking. Therefore, we aimed to establish a unified formalized classification system based on a large data set of vegetation plots covering the entire range of these forests. Location: Europe, Anatolia, Caucasus and northern Iran. Methods: We compiled a data set of 15,817 vegetation plots from the European Vegetation Archive and the Hyrcanian Forest Vegetation Database, using the formal definition of the EUNIS habitat type T1E Carpinus and Quercus mesic deciduous forest. We classified the data set using TWINSPAN. Biogeographically and ecologically similar plot clusters were merged into oak–hornbeam forest types, which were interpreted as alliances. We also developed expert systems for automatically classifying vegetation at the alliance level for both the EuroVegChecklist (EVC) system and the revised classification. In addition, we calculated ordinations to show the major gradients in the species composition of the data set. Results: We present a revised classification system of the order Carpinetalia betuli with nine alliances, including basic descriptions of their species composition, distribution, ecology and syntaxonomy. The analyses largely supported the biogeographic concept of classification, analogous to EVC. Compared to EVC, we recognized an additional alliance Physospermo verticillati‐Quercion cerridis (southern Italy) but found no support for the alliances Astrantio‐Carpinion, Erythronio‐Carpinion and Scillo‐Quercion. The greatest difference in species composition was found between the southern and northern‐northeastern Carpinetalia types. Expert systems for the revised classification system (~89% of plots classified) and the EVC system (~72%) are also included. Conclusions: We provide the first comprehensive overview of alliances of the order Carpinetalia betuli across its whole distribution range. The associated expert systems allow consistent application of the classification of these forests in nature conservation, habitat monitoring, and biodiversity and ecological research.We provide the first formal classification for oak–hornbeam forests and related vegetation types (phytosociological order Carpinetalia betuli) across Europe and adjacent areas. It includes both traditional and revised classifications of this vegetation. Furthermore, we developed expert systems for vegetation‐plot assignment to vegetation types, which can be applied in research and biodiversity conservation, monitoring and management. [ABSTRACT FROM AUTHOR]

We report on the completed third volume of Vegetation Classification and Survey (VCS). VCS has been included in the Scopus bibliometric database and will receive its first CiteSore in mid-2023. We announce the 2022 Editors' Award for a paper selected from the four papers nominated for Editors' Choice during 2022. We selected Liu et al. (2022; Vegetation Classification and Survey 3: 121-144) for the Editors' Award. This author team developed a comprehensive hierarchical classification system for the steppe vegetation over China. We present five Special Collections (two concluded and three ongoing) which form a backbone for VCS. Apart from Research Papers, Long and Short Database Reports were the prevailing article category in 2022. By contrast, there were no VCS Methods paper in 2022, and thus we encourage submissions particularly in this category. Finally, we welcome new members to the Editorial Board and open a call for free applications for our Editorial Review Board or as a Linguistic Editor. [ABSTRACT FROM AUTHOR]

The occurrence and origin of dry grasslands and their rich biota in the moderately humid Central‐European climate have fascinated scientists for over a century. Modern palaeoecological and phylogeographical data support earlier hypotheses that these grasslands are late Pleistocene relicts and can therefore be considered part of the Eurasian forest–steppe biome. However, it is still unclear which factors fostered the maintenance of steppe patches in Central Europe throughout the Holocene. Here, we provide an overview of the main hypotheses, which stress, respectively, the effects of climate, edaphic conditions and disturbances. We then develop a general conceptual framework on how these three factors interact to form forest–steppe mosaics. We thereby emphasize the role of topography as a crucial control on forest–steppe patterns at the landscape scale. Topography is related to several mechanistic drivers that influence vegetation processes, such as near‐surface microclimate and soil formation. Consequently, topographic variation allows both forest and steppe patches to occur beyond their macroclimatic niche, favouring the development of forest–steppe mosaics. To illustrate our framework, we demonstrate the interactive effect of macroclimate and topography on the occurrence of steppe patches at 108 selected Central European forest–steppe sites. Although we developed our framework focusing on the current distribution of Central European forest–steppe, we suggest that it contributes to the understanding of similar transitions between temperate forest and steppe biomes in the past as well as elsewhere in the world. [ABSTRACT FROM AUTHOR]

The importance of environmental difference among sites and dispersal limitations of species to the explanation of diversity differs among biological systems and geographical regions. We hypothesized that climate and then dispersal limitation will predominantly explain the similarity of alpine vegetation at increasing distances between pairs of regions at subcontinental extent. We computed the similarity of all pairs of 23 European mountain regions below 50° N after dividing the species lists of each region by calcareous or siliceous substrates. Distance decay in similarity was better fitted by a cubic polynomial than a negative exponential function, and the fit was better on calcareous than on siliceous substrate. Commonality analysis revealed that the proportion of explanation of beta diversity by climatic difference had unimodal patterns on a gradient of increasing distance between regions, while explanation by dispersal limitation had consistently rising patterns on both substrates. On siliceous substrate, dispersal limitation explained more of the variation in beta diversity only at longer distances, but it was predominant at all distances on calcareous substrate. The steeper response to distance at <1600 km and >2600 km may indicate dispersal limitation at different temporal scales, and the uptick in the response to distance at the longest distances may reflect how isolated some regions have been before and since the last glacial maximum. [ABSTRACT FROM AUTHOR]

Aim: The steppe grasslands of eastern Central Europe are exceptionally species rich and valuable from a nature conservation point of view. However, their historical biogeography is still poorly understood. Here we use the regional diversity of habitat specialists and chloroplast DNA data to investigate potential long-term refugia of steppe species in this region. Location: Pannonian Basin and adjacent regions; SW Russia. Taxon: Vascular plants. Methods: After identifying habitat specialists of the three main steppe types (meadow steppes, grass steppes and rocky steppes), we compiled their regional presence--absence in grid cells of 75 km x 75 km. We analysed the dependency of habitat specialist diversity to climate, topographic heterogeneity and geographical distance to potential refugia. For genetic analysis, we sampled three or four habitat specialists of each steppe type and used cpDNA markers to investigate intraspecific diversity and geographical distribution of haplotypes. We also tested for correspondence between the number of habitat specialists and haplotype diversity. Results: Climate and topography explained between 40% and 63% of the variance in habitat specialist diversity. Adding geographical distance to potential refugia increased the explained variance in the models for all steppe types. Chloroplast haplotypes featured a complex pattern across the study area. Several species showed a strong geographical differentiation, suggesting migration waves from multiple refugia with only limited subsequent genetic intermixture. Maximum haplotype diversity in a region showed a better correlation with the number of habitat specialists per steppe type than mean haplotype diversity. Main conclusions: We can clearly reject the scenario of a late-Holocene immigration of steppe species from areas outside the Pannonian Basin. Most species must have been present in the region since at least the early Holocene, highlighting the importance of the lower mountain ranges surrounding the Pannonian Basin as long-term refugia for European steppe species. Dispersal limitation and resulting migration lags seem to have a strong influence on the distribution of steppe species in Central Europe. [ABSTRACT FROM AUTHOR]

The fourth edition of the International Code of Phytosociological Nomenclature (ICPN) was prepared by the Steering Committee of the IAVS Working Group for Phytosociological Nomenclature (GPN). The edition consists of 14 Definitions, 7 Principles, 53 Articles, and 7 Appendices. When compared with the previous edition, the main amendments are: (a) the acceptance of electronic publications (Art. 1); (b) the introduction of binding decisions (Definition XIV, Principle II, Articles 1, 2b, 3c, 29b, 40, 42, 44, Appendices 6 and 7); (c) the mandatory use of the English or Latin terminology for syntaxonomic novelties (Definition II, Principle II, Articles 3d and 3i); (d) the introduction of autonyms for the main ranks when the corresponding secondary ranks are created (Articles 13b and 24); (e) the automatic correction of the taxon names (name‐giving taxa) used in the names of syntaxa in accordance with the International Code of Nomenclature for algae, fungi, and plants (ICN) (Article 44); (f) the possibility to mutate the name of a syntaxon in using other correct, alternative names for the name‐giving taxa (Article 45); (g) the introduction of inadequate names, a new category of rejected names (Definition V, Articles 43 through 45); and (h) the introduction of a conserved type (Definition XIII, Article 53). The fourth edition of ICPN was approved by the GPN on 25 May 2019 and becomes effectively binding on 1 January 2021. [ABSTRACT FROM AUTHOR]

Aims: The effect of biogeographical processes on the spatial turnover component of beta‐diversity over large spatial extents remains scarcely understood. Here, we aim at disentangling the roles of environmental and historical factors on plant taxonomic and phylogenetic turnover, while controlling for the effects of species richness and rarity. Location: European beech (Fagus sylvatica) forests in Europe. Methods: We aggregated plant species occurrences from vegetation plots in spatial grid cells of 0.25º × 0.25º to calculate the spatial turnover component of taxonomic (TBDturn) and phylogenetic (PBDturn) beta‐diversity for each cell. We also calculated the deviation of PBDturn given TBDturn (PBDdev‐turn), which measures the importance of phylogenetic turnover after factoring out taxonomic turnover. Beta‐diversity was calculated for each grid cell as the mean pairwise dissimilarity between the focal cell and all other cells. We used structural equation modeling (SEM) to examine the relationships between environmental (climate, soil pH, and distance from the geographical distribution limit of beech) and historical (distance from beech glacial refugia) predictors and beta‐diversity metrics. Results: We found a geographically consistent variation in taxonomic and phylogenetic turnover. Overall, TBDturn and PBDturn increased significantly toward more extreme climatic conditions, on more acidic soils, and toward the margins of beech distribution. The effects of environmental variables and the distance from glacial refugia on beta‐diversity metrics were mediated by species richness and rarity. Phylogenetic turnover was low in relation to taxonomic turnover (i.e., high PBDdev‐turn) in areas closer to glacial refugia. Conclusions: Continental‐scale patterns of beta‐diversity in European beech forests are the result of complementary ecological and evolutionary processes. In general, beech forests are taxonomically and phylogenetically more distinct in climatically marginal areas of their European range. However, the spatial variation of beta‐diversity in European beech forest flora is still strongly characterized by the distribution of groups of closely related species that evolved or survived in glacial refugia. [ABSTRACT FROM AUTHOR]

In this Report, three previously published nomenclatural proposals are discussed, and recommendations on acceptance or rejection of these proposals are provided. The proposals concern the following syntaxa: Berberidion Braun-Blanquet 1950, Aceretalia pseudoplatani Moor 1976 and Festucetalia valesiacae Braun-Blanquet et Tüxen ex Braun-Blanquet 1950. [ABSTRACT FROM AUTHOR]

Aims: To link the Braun-Blanquet units of the EuroVegChecklist (EVC) with the upper levels of the International Vegetation Classification (IVC), and to propose a division level classification for Europe. Study area: Europe. Methods: We established a tabular linkage between EVC classes and IVC formations and identified mismatches between these two levels. We then proposed IVC division level units to organize EVC classes. Results: We organized the EVC classes into 21 formations and 30 divisions. We flagged classes that did not fit comfortably within an existing formation, either because its content corresponded to more than one formation or because it did not fit any formation description. In a few cases, we split EVC classes because they seemed too heterogenous to be assigned to a single formation. Conclusions: The IVC approach adds a set of physiognomic and ecological criteria that effectively organizes the EVC classes, which are already being increasingly informed by physiognomy. Therefore, the formation concepts are relatively natural extensions of concepts already embedded in the classes. However, physiognomic placement of Braun-Blanquet classes can be difficult when the sampling of the vegetation is at finer grain than usual in the respective formation (tall-scrub, annual pioneer communities). Some EVC classes seem too heterogenous to fit into the IVC formation system. Delimitation of these classes has often been a matter of debate for many decades, and the IVC perspective might help to solve these intricate issues. In other cases, mismatches between phytosociological classes and IVC formations might better be solved by emending the current formation concepts. [ABSTRACT FROM AUTHOR]

Aims: We studied the syntaxonomic position, biodiversity, ecological features, nature conservation value and current status of dry grasslands investigated by Josias Braun-Blanquet more than 60 years ago. Study area: Inner-alpine valleys of Austria. Methods: We sampled 67 plots of 10 m2, following the standardized EDGG methodology. We subjected our plots to an unsupervised classification with the modified TWINSPAN algorithm and interpreted the branches of the dendrogram syntaxonomically. Biodiversity, structural and ecological characteristics of the resulting vegetation units at association and order level were compared by ANOVAs. Results: All the examined grasslands belong to the class Festuco-Brometea. From ten distinguished clusters, we could assign four clusters to validly published associations, while the remaining six clusters were named tentatively. We classified them into three orders: Stipo-Festucetalia pallentis (Armerio elongatae-Potentilletum arenariae, Phleo phleoidis-Pulsatilletum nigricantis, Medicago minima-Melica ciliata community, Koelerio pyramidatae-Teucrietum montani), Festucetalia valesiacae (Sempervivum tectorum-Festuca valesiaca community); Brachypodietalia pinnati (Astragalo onobrychidis-Brometum erecti, Agrostis capillaris-Avenula adsurgens community, Anthericum ramosum-Brachypodium pinnatum community, Ranunculus bulbosus-Festuca rubra community, Carduus defloratus-Brachypodium pinnatum community). Conclusions: The ten distinguished dry grassland communities of the Austrian inner-alpine valleys differ in their ecological affinities as well as their vascular plant, bryophyte and lichen diversity. We point out their high nature conservation importance, as each of them presents a unique habitat of high value. [ABSTRACT FROM AUTHOR]