Journal articles on the topic 'Bryophytes – Classification'

Эпифитные и эпиксильные виды мохообразных и лишайников могут выступать в качестве диагностических не только при дифференциации своих синузий, но и на уровне лесного сообщества в целом, формируя единые детерминантные группы вместе с сосудистыми растениями и эпигейными мхами. Это подтверждают результаты доминантно-детерминантной классификации широколиственных лесов, описанных в заповедниках «Калужские засеки» и «Мордовский». В обоих случаях выделенные синтаксоны поддаются флористической дифференциации с помощью не только сосудистых растений, но и эпифитных мохообразных. При необходимости их можно было бы разграничить исключительно по видам эпифитной бриосинузии. Формирование единых детерминантных групп обусловлено влиянием факторов, единообразно воздействующих на все виды, входящие в эти группы. Первостепенную роль предположительно играют микроклиматические факторы, особенно влажность и амплитуды температур приземного слоя воздуха. Эдафические факторы не оказывают прямого влияния на сопряженность видов сосудистых растений и эпифитных мохообразных, но их косвенное влияние также может быть существенным. Piphytic and epixylic species of bryophytes and lichens may serve as determinants in differentiation of not only their synusiae but also at the level of forest plant communities where they grow, forming integrated differential groups together with vascular plant and epigeic bryophyte species. This is proved by the results of the broadleaved forest classification, performed following the complex dominant-determinant approach in the Kaluzhskie Zaseki (see Table 1) and Mordovian (see Table 2) nature reserves, Russia. All the recognized broadleaved-forest syntaxa are subject to distinct floristic differentiation with the help of both vascular and epiphytic bryophyte species under ecologically contrasting habitat conditions. Moreover, if necessary, these syntaxa can be distinguished using the epiphytic species only. The ecological and phytocoenotical association of vascular and epiphytic bryophyte species presumably originates due to microclimatic factors such as air humidity and temperature ranges near the ground. Edaphic factors do not influence the association of vasculars and epiphytic bryophytes within the integrated determinant groups directly, but their indirect influence may be also essential.

The central aim in ecometabolomics and chemical ecology is to pinpoint chemical features that explain molecular functioning. The greatest challenge is the identification of compounds due to the lack of constitutive reference spectra, the large number of completely unknown compounds, and bioinformatic methods to analyze the big data. In this study we present an interdisciplinary methodological framework that extends ultra-performance liquid chromatography coupled to electrospray ionization quadrupole time-of-flight mass spectrometry (UPLC/ESI-QTOF-MS) with data-dependent acquisition (DDA-MS) and the automated in silico classification of fragment peaks into compound classes. We synthesize findings from a prior study that explored the influence of seasonal variations on the chemodiversity of secondary metabolites in nine bryophyte species. Here we reuse and extend the representative dataset with DDA-MS data. Hierarchical clustering, heatmaps, dbRDA, and ANOVA with post-hoc Tukey HSD were used to determine relationships of the study factors species, seasons, and ecological characteristics. The tested bryophytes showed species-specific metabolic responses to seasonal variations (50% vs. 5% of explained variation). Marchantia polymorpha, Plagiomnium undulatum, and Polytrichum strictum were biochemically most diverse and unique. Flavonoids and sesquiterpenoids were upregulated in all bryophytes in the growing seasons. We identified ecological functioning of compound classes indicating light protection (flavonoids), biotic and pathogen interactions (sesquiterpenoids, flavonoids), low temperature and desiccation tolerance (glycosides, sesquiterpenoids, anthocyanins, lactones), and moss growth supporting anatomic structures (few methoxyphenols and cinnamic acids as part of proto-lignin constituents). The reusable bioinformatic framework of this study can differentiate species based on automated compound classification. Our study allows detailed insights into the ecological roles of biochemical constituents of bryophytes with regard to seasonal variations. We demonstrate that compound classification can be improved with adding constitutive reference spectra to existing spectral libraries. We also show that generalization on compound classes improves our understanding of molecular ecological functioning and can be used to generate new research hypotheses.

Mosses and hepatics (bryophytes) are the most diverse and abundant understorey vegetation within the Coastal Western Hemlock (CWH) and Interior Cedar–Hemlock (ICH) zones of British Columbia. This study intensively sampled bryophytes in 287 young- and old-growth stands in the CWH and ICH zones. Two major variables strongly influence the patterning of bryophyte diversity in these zones: stand age and habitat heterogeneity. Canonical correspondence analyses (CCA) identified these as the most important variables explaining stand–environment interactions. Alpha diversity is much greater in old-growth forests and beta diversity is high between young and old forests. Old-growth cedar–hemlock forests have between 60 (ICH) and 100% (CWH) more species than younger forests disturbed by wildfire in the ICH zones or logging in the CWH zones. Furthermore, a stand classification built on species composition partitioned species into stands of different ages and mesohabitat heterogeneity. Beta diversity was also partitioned between stands of different ages and habitat heterogeneity. This indicates that both young and old forests have a unique assemblage of species. Indicator analysis was used to choose a partial lists of species that are indicators of "old growthness". These old forests support a rich flora of hepatics and rare western North American endemics. High environmental continuity is associated with the most humid watersheds and cedar–hemlock forests within these watersheds have the highest bryophyte diversity. The establishment of rich communities of bryophytes in the moist cedar–hemlock forest has been occurring over the last 2000–7000 years, with the coastal rainforest much older than the inland rainforest. Large-scale disturbance, such as forestry, threatens the existence of these highly diverse communities. A better understanding of the patterning of bryophyte diversity will provide an opportunity to minimize the impact of forest operations on biodiversity. Bryophyte diversity in British Columbia cedar–hemlock forests will be sustained through ecosystem management of old-growth legacies (i.e., landscapes, stands, and their components) and preservation of areas of high diversity. Temporal and habitat variables are influential in the patterning of bryophyte diversity. Management plans that consider these variables will be better equipped to manage cedar–hemlock forests for maintaining biodiversity. Key words: biodiversity, bryophytes, cedar–hemlock, CWH, disturbance, ecosystem management, floristic habitat sampling, forest conservation, ICH, old growth, patterning of diversity, rare species, species richness.

In plant ecology, biochemical analyses of bryophytes and vascular plants are often conducted on dried herbarium specimen as species typically grow in distant and inaccessible locations. Here, we present an automated in silico compound classification framework to annotate metabolites using an untargeted data independent acquisition (DIA)–LC/MS–QToF-sequential windowed acquisition of all theoretical fragment ion mass spectra (SWATH) ecometabolomics analytical method. We perform a comparative investigation of the chemical diversity at the global level and the composition of metabolite families in ten different species of bryophytes using fresh samples collected on-site and dried specimen stored in a herbarium for half a year. Shannon and Pielou’s diversity indices, hierarchical clustering analysis (HCA), sparse partial least squares discriminant analysis (sPLS-DA), distance-based redundancy analysis (dbRDA), ANOVA with post-hoc Tukey honestly significant difference (HSD) test, and the Fisher’s exact test were used to determine differences in the richness and composition of metabolite families, with regard to herbarium conditions, ecological characteristics, and species. We functionally annotated metabolite families to biochemical processes related to the structural integrity of membranes and cell walls (proto-lignin, glycerophospholipids, carbohydrates), chemical defense (polyphenols, steroids), reactive oxygen species (ROS) protection (alkaloids, amino acids, flavonoids), nutrition (nitrogen- and phosphate-containing glycerophospholipids), and photosynthesis. Changes in the composition of metabolite families also explained variance related to ecological functioning like physiological adaptations of bryophytes to dry environments (proteins, peptides, flavonoids, terpenes), light availability (flavonoids, terpenes, carbohydrates), temperature (flavonoids), and biotic interactions (steroids, terpenes). The results from this study allow to construct chemical traits that can be attributed to biogeochemistry, habitat conditions, environmental changes and biotic interactions. Our classification framework accelerates the complex annotation process in metabolomics and can be used to simplify biochemical patterns. We show that compound classification is a powerful tool that allows to explore relationships in both molecular biology by “zooming in” and in ecology by “zooming out”. The insights revealed by our framework allow to construct new research hypotheses and to enable detailed follow-up studies.

AbstractThe aim of the present study was to determine a relationship between physiological traits and functional types of bryophytes from five boreonemoral habitats with a particular emphasis on discriminative ability of these traits. Sampling of 25 species was performed four times during one season. Water content, chlorophyll a fluorescence and photosynthetic pigment concentration were measured in field and water-equilibrated samples. Principal component analysis indicated the existence of an inverse relationship between concentration of pigments and water content. Linear discriminant analysis showed that relatively high mean predicted posterior probabilities of correct classification of functional types by physiological traits were found for water conducting system, followed by substrate and habitat, but it was highly variable and type-specific for life form and relatively less variable for life strategy. Field water content had the highest average discriminative importance among physiological traits, followed by chlorophyll fluorescence indices field Fv/Fm, equilibrated PI, equilibrated RC/ABS, and field RC/ABS. Photosynthetic pigment concentrations had relatively less average importance for classification of functional types.

By mean of a line-taxation (ordination), the floristic discontinuities of epiphytic bryophytes were shown within an altitudinal gradient from the eastern Congo basin to the mountains of the Riftvalley (Mt. Kahuzi) (BRYOTROP III-transect). By this ordination, the epiphytic vegetation can be grouped into four ecological groups, indicating the climatic factors. They show a strong correlation to the known altitudinal zonation, the different forest zones, and the plantsociological classification. These groups consist of taxa of different relationships which grow and evolve under similar environmental conditions.

Alterations to the inventory of about 24 000 species and infraspecific taxa of bryophytes and vascular plants in southern Africa are reported for the year 1987. The inventory, as presently maintained in the Taxon component of the PRECIS system, contains the accepted name for each taxon, synonyms previously in use as accepted names during the past half-century, and literature references necessary to identify species in each genus and to establish the synonymy. The inventory is updated as new research affecting plant classification in southern Africa is published. During 1987 there were 678 alterations, representing about 2,8% of the total number of taxa.a

Alterations to the inventory of about 24 000 species and infraspecific taxa of bryophytes and vascular plants in southern Africa are reported for the year 1988. The inventory, as currently maintained in the Taxon component of the PRECIS system, contains the accepted name for each taxon, synonyms previously in use as accepted names during the past half-century, and literature references necessary to identify species in each genus and to establish the synonymy. The inventory is updated as new research affecting plant classification in southern Africa is published. During 1988 there were 744 alterations, affecting about 3% of the total number of taxa.

AbstractThe maintenance of protected lichen species and their biodiversity in general depends on good management practices based on their distribution and habitat preferences. To date, 10 of the 17 protected lichen species of Hungary have been recorded in the Bakony Mts including the Balaton Uplands region. Habitat preferences of three protected Cladonia species (C. arbuscula, C. mitis and C. rangiferina) growing on underlying rocks of red sandstone, basalt, Pannonian sandstone and gravel were investigated by detailed sampling. We recorded aspect, underlying rock type, soil depth, pH and CaCO3 content, habitat type (as defined by the General National Habitat Classification System Á-NÉR), all species of lichen, bryophyte and vascular plants as well as percentage cover of exposed rock, total bryophytes, lichens, vascular plants and canopy, degree of disturbance and animal impacts. Sporadic populations of these species mostly exist at the top of hills and mountains in open acidofrequent oak forests, but they may occur in other habitats, such as closed acidofrequent oak forests, slope steppes on stony soils, siliceous open rocky grasslands, open sand steppes, wet and mesic pioneer scrub and dry Calluna heaths. Cladonia rangiferina was found to grow beneath higher canopy cover than either C. arbuscula or C. mitis in the Balaton Uplands. Furthermore, there were significant differences in canopy cover between occupied and unoccupied quadrats in the case of all three species. Cladonia rangiferina is a good indicator species of natural habitats in Hungary due to its restricted distribution and low ecological tolerance. These results may lead to the adoption of effective conservation methods (e.g. game exclusion, artificial dispersal) in the future.

Fourier transform infrared spectroscopy (FT-IR) with Horizontal Attenuated Total Reflectance (HATR) techniques is used to obtain the FT-IR spectra of five kinds of mosses, such asPtychomitrium dentatum(Mitt.) Jaeg.,Ptychomitrium polyphylloides(C. Muell.) Par.,Ptychomitrium sinense(Mitt.) Jaeg.,Macromitrium syntrichophyllumTher. Etp. Vard., andMacromitrium ferrieiCard. Sz Ther. Based on the comparison of the above mosses in the FT-IR spectra, the region ranging from 4000 to 650 cm−1was selected as the characteristic spectra for analysis. Principal component analysis (PCA) and cluster analysis are considered to identify the five moss species. Because they belong to the homogeneous plants, and have similar chemical components and close FT-IR spectroscopy, PCA and cluster analysis can only give a rough result of classification among the five moss species, Fourier self-deconvolution (FSD) and discrete wavelet transform (DWT) methods are used to enhance the differences between them. We use these methods for further study. Results show that it is an excellent method to use FT-IR spectroscopy combined with FSD and DWT to classify the different species in the same family. FT-IR spectroscopy combined with chemometrics, such as FSD and DWT, can be used as an effective tool in systematic research of bryophytes.

Abstract Swamp forests dominated by Picea abies contribute strongly to the total plant species richness in boreal forests. The variation in species composition and environmental conditions in swamp forests and the relationships of swamp forests to mires and upland forest, have, however, remained insufficiently known. From a preliminary survey of 57 spruce swamp forests, eleven localities were selected to represent the variation in the study area with respect to size and nutrient status, and altitude and position in the landscape. Physiographic and hydrotopographic descriptions were made. A total of 150 1-m2 plots were distributed on the localities by a restricted random procedure. In each plot, the abundance of all vascular plants, bryophytes and macrolichens was recorded as frequency in 16 subplots, 53 variables (topographic and geographic, tree influence, water-table, water chemical and physical, and soil chemical and physical) were measured. The gradient ( coenocline) structure of vegetation was found by parallel DCA and LNMDS ordinations, interpreted ecologically by analysis of correlations and geostatistical patterns. The two main coenoclines were the same for the full species composition and for vascular plant and cryptogams considered separately. The first gradient was related to soil acidity and nutrient concentrations: plots segregated into relatively poor (and intermediate) and richer swamp forests. Nitrogen availability is considered a decisive factor for species’ responses to this gradient. The second gradient was related to depth to the water table and mesotopographic relief of the swamp-forest surface, varying mostly on fine (0.75-1.5 m) scales. Vascular plants segregate along this gradient due to a trade-off between tolerances to waterlogging and drought, bryophyte are influenced by a complex set of factors. Two minor vegetation gradients were also found; one related to microtopography (extending from flat, lawn-like areas dominated by large bryophytes to more strongly sloping sites dominated by small mosses and hepatics; ‘pocket species’) and one weakly related to the annual water-table amplitude. Relatively strong coenoclines were found that separated entire swamp forests but were uncorrelated with measured variables. These occurred because all swamp forests, notably the richer, had a strong element of uniqueness in species composition, probably because species are recruited from a large species pool during thousands of years. Swamp forest is proposed as a broad term for all peatlands with trees, including mire margin, from which it is essentially indistinguishable. Similarities with, and differences from, open mire and forest on mineral soil are discussed. Some unique features of swamp forests are pointed out. A classification of swamp forests into eight site-types by division of the two main gradients is proposed. Descriptions are provided for the six site-types encountered in the study area. All intact richer swamp forests and a representative selection of poor swamp forests should be protected if maintenance of the biological diversity of (coniferous) forests in general, and swamp forests in particular, is aimed at.

In the last few years, the occurrence and abundance of tree-related microhabitats and habitat trees have gained great attention across Europe as indicators of forest biodiversity. Nevertheless, observing microhabitats in the field requires time and well-trained staff. For this reason, new efficient semiautomatic systems for their identification and mapping on a large scale are necessary. This study aims at predicting microhabitats in a mixed and multi-layered Mediterranean forest using Airborne Laser Scanning data through the implementation of a Machine Learning algorithm. The study focuses on the identification of LiDAR metrics useful for detecting microhabitats according to the recent hierarchical classification system for Tree-related Microhabitats, from single microhabitats to the habitat trees. The results demonstrate that Airborne Laser Scanning point clouds support the prediction of microhabitat abundance. Better prediction capabilities were obtained at a higher hierarchical level and for some of the single microhabitats, such as epiphytic bryophytes, root buttress cavities, and branch holes. Metrics concerned with tree height distribution and crown density are the most important predictors of microhabitats in a multi-layered forest.

AbstractSigny Island has experienced a dramatic increase in fur seal numbers over recent decades, which has led to the devastation of lowland terrestrial vegetation, with the eradication of moss turfs and carpets being the most prominent feature. Here we demonstrate that fur seals also affect the other major component of this region’s typical cryptogamic vegetation, the lichens, although with a lower decrease in variability and abundance than for bryophytes. Classification (UPGMA) and ordination (Principal Coordinate Analysis) of vegetation data highlight differences in composition and abundance of lichen communities between areas invaded by fur seals and contiguous areas protected from these animals. Multivariate analysis relating lichen communities to environmental parameters, including animal abundance and soil chemistry (Canonical Correspondence Analysis), suggests that fur seal trampling results in the destruction of muscicolous-terricolous lichens, including several cosmopolitan and bipolar fruticose species. In addition, animal excretion favours an increase in nitrophilous crustose species, a group which typically characterizes areas influenced by seabirds and includes several Antarctic endemics. The potential effect of such animal-driven changes in vegetation on the fragile terrestrial ecosystem (e.g. through modification of the ground surface temperature) confirms the importance of indirect environmental processes in Antarctica.

The <em>Isoëto-Nanojuncetea</em>-class includes short-lived and ephemerical communities occurring on temporarily flooded places in Western, Southern and Central Europe and Northern Africa. Results of the numerical classification of 739 phytosociological releves of the communities occurring in Poland are presented and discussed. Ali the releves were made in accordance with the principles of the BRAUN-BLANQUET school of syntaxonomy. The calculations were performed using NCLAS program of the SYN-TAX IV package. The JACCARD formuła and the unweighted pair-group method, using arithmetic averages (UPGMA) were applied. There is a strong habitat and floristic differentation of the communities of the <em>Isoëto-Nanojuncetea</em>-class occurring in Poland. The results of the numerical classification indicate that, the distuinguished communities belong to two alliances: the <em>Radiolion linoidis</em> (Rivas Goday 1961) Pietsch 1965 (for associations occurring on synanthropic localities like stubble fields) and the <em>Elatini-Eleocharition ovatae</em> Pietsch 1965 (for communities growing on bottoms of dried ponds and exposed river or lakę banks). The distinguished communities arę phytosociologically characterized on basis of 223 selected releves. These arę: <em>Spergulario-Illecebretum verticillati, Ranunculo-Myosuretum minimi, Centaurium pulchellum-Pottia truncata-commumiy, Heleocharetum ovatae, Cyperetum flavescentis</em> and <em>Cyperus fuscus-Limosella aquatica</em>-commumiy. The study focused on: (1) attempting to solve the problem of phytosociological classification for the communities occurring in Poland, (2) preparing a complete catalogue of them and (3) giving the full list of character species (also among bryophytes) of distinguished syntaxa. It has led to finding out the relation between the communities occurring in Poland and the associations of Western Europe. The problem of the naturality of certain distinguished associations was discussed. The paper gives also some open questions demanding further studies and some suggestions of methods to be applied.

AbstractA directional primary succession with moderate species replacement was quantitatively characterized on Signy Island in zones of a glacial valley corresponding to their age since deglaciation. A continuous increase in diversity and abundance of lichens and bryophytes was observed between terrains deglaciated in the late 20th century, to areas where deglaciation followed the Little Ice Age, and others thought to be ice-free since soon after the Last Glacial Maximum. Classification (UPGMA) and ordination (principal co-ordinate analysis) of vegetation data identified three different stages of development: a) pioneer communities, which rapidly develop in a few decades, b) immature communities developing on three to four century old terrains, and c) a climax stage (Polytrichum strictum-Chorisodontium aciphyllum community) developing on the oldest terrains, but only where local-scale environmental features are more favourable. Multivariate analysis including environmental parameters (canonical correspondence analysis) indicated terrain age as being the dominant controlling factor, with other environmental factors also exhibiting significant conditional effects (duration of snow cover, surface stoniness). These findings not only quantitatively verify reports of the rapid colonization of Maritime Antarctic terrains following recent climate amelioration and associated decrease in glacial extent, but also show how local-scale environmental resistance may slow or even prevent vegetation succession from pioneer to more mature stages in future.

Light-harvesting-like (LIL) proteins are low-molecular-mass membrane proteins related to the light-harvesting complexes, which form the dominant antenna system in most photosynthetic eukaryotes. To analyze the LIL protein family, we mined a number of publicly available databases to identify members of this family in a broad range of organisms. LIL proteins are diverse, having one to three predicted transmembrane helices. One- and two-helix LIL proteins were found in all the major photosynthetic eukaryote lineages (glaucophytes, red algae, and green algae) and are particularly well conserved in the green algae and land plants. In most cases, however, these proteins are not conserved between major lineages, and in some cases appear to have evolved independently. Three-helix LIL proteins are well conserved within the gymnosperms and angiosperms, but are much more divergent, and have been duplicated multiple times, in the green algae and bryophytes. We also identified a novel LIL protein in two Micromonas strains that contains a fourth hydrophobic region. This analysis identifies conserved members of the LIL protein family, signifying their importance to photosynthetic eukaryotes. It also indicates that classification of these proteins based on structural characteristics alone inadequately reflects the evolutionary history observed in this complex protein family.

ABSTRACTVolcán Barva, Costa Rica, has on its northern slope an unbroken sequence of rain forest on volcanic parent materials from near sea level at La Selva Field Station up to its summit at 2906 m. It provides a good area to study forest changes with altitude and their causes. In the present paper we describe the forests as a background for soil and litterfall studies from 1 ha plots at each of the following altitudes: 100 m, 500 m, 1000 m, 1500 m, 2000 m and 2600 m. The canopy heights (with height of the highest emergent in parentheses) ranged from 35–40 m (45 m) at 100 m to 20–23 m (32 m) at 2600 m; basal area was least (22.7 m2) at 100 m and highest (51.2 m2) at 2600 m; the tree (≥10 cm dbh) density ranged from 391 ha–1at 500 m to 617 ha–1 at 2600 m. Most trees were identified and on samples of them we recorded presence of buttresses, lianes, skiophytic climbers, vascular epiphytes and bryophytes; and drew profile diagrams. In the classification of Whitmore (1984) the two lower plots are evergreen lowland rain forests; the other four are lower montane rain forest. Species richness was highest in the plot at 500 m, with at least 135 species of tree, and least at 2600 m, with at least 35 species. The Volcán Barva forest altitudinal sequence is briefly compared with those elsewhere.

The classification of synusial epigeic and epiphytic bryophyte communities of forest coenoses of forest-steppe zone of UkraineThe syntaxonomical classification and characteristics of synusial epigeic and epiphytic bryophyte communities of forest coenoses of forest-steppe zone of Ukraine is presented in this paper.

AbstractCanadian peatlands can be classified into ombrotrophic bogs and minerotrophic fens, the latter subdivided into poor, moderate-rich, and extreme-rich fens, each with distinctive indicator species, acidity, alkalinity, and base cation content. If hydrology is considered the most important factor in peatland classification then the primary division must be between ombrotrophic bogs and minerotrophic fens; however both chemical and vegetational differences strongly indicate that the primary division of peatlands should be between acidic, Sphagnum-dominated bogs and poor fens on the one hand, and alkaline, brown-moss-dominated rich fens on the other. Although some metals such as sulphur and aluminum also vary along this gradient, nutrient contents of the surface waters do not. Bogs and fens are oligotrophic to mesotrophic wetlands that should be distinguished from eutrophic, non-peat-forming wetlands such as marshes and swamps by the presence in the former of a well-developed ground layer of bryophytes associated with relatively little seasonal water level fluctuation. Oligotrophy is probably maintained in bogs and poor fens by reduced water flow, whereas rich fens maintain mesotrophy by having larger water through-puts; however this is not well documented. Sphagnum appears to have real ecological significance, both in the initial stages of acidification and in controlling surface water temperature. Seasonal variation in surface water chemistry in all peatland types is relatively small, however precipitation events leading to changes in water levels do affect some chemical components. Although both autogenic and allogenic factors affect peatland development, initiation of peat formation and early development of peatlands during the Early and Mid Holocene were considerably influenced by regional climatic change. Later developmental patterns during the late Holocene and those seen at the present time appear to be more influenced by autogenic factors.

This study aimed at an investigation of the structure, ecology and mapping of mixed communities with the participation of spruce, pine and broad-leave trees in one of the regions of broad-leave–coniferous zone. Despite the long history of the nature use of the study area, including forestry practices (Kurnayev, 1968; Rysin, Saveliyeva, 2007; Arkhipova, 2014; Belyaeva, Popov, 2016), the communities kept the main features of the indigenous forests of the broad-leave–coniferous zone ­— the tree species polydominance of the stands, the multilayer structure of communities and the high species diversity. In the course of field works in the southwestern part of the Moscow Region (2000–2016) 120 relevés were made. Spatial structure, species composition as well as cover values (%) of all vascular plants and bryophytes were recorded in each stand. The relevés were analysed following the ecology-phytocenotic classification approach and methods of multivariate statistical analysis that allowed correctly to differentiate communities according the broad-leave species participation. The accuracy of the classification based on the results of discriminant analysis was 95.8 %. Evaluation of the similarity of the selected units was carried out with the help of cluster analysis (Fig. 12). Clustering into groups is performed according to the activity index of species (A) (Malyshev, 1973) within the allocated syntaxon using Euclidean distance and Ward’s method. The classification results are corrected by DCA ordination in PC-ORD 5.0 (McCune, Mefford, 2006) (Fig. 1). Spatial mapping of forest cover was carried out on the basis of ground data, Landsat satellite images (Landsat 5 TM, 7 ETM +, 8 OLI_TIRS), digital elevation (DEM) and statistical methods (Puzachenko et al., 2014; Chernenkova et al., 2015) (Fig. 13 а, б). The obtained data and the developed classification refine the existing understanding of the phytocenotic structure of the forest cover of the broad-leave–coniferous zone. Three forest formation groups with different shares of broad-leave species in the canopy with seven groups of associations were described: a) coniferous forests with broad-leave species (small- and broad-herb spruce forests with oak and lime (1)); broad-herb spruce forests with oak and lime (2); small- and broad-herb pine forests with spruce, lime, oak and hazel (3); broad-herb pine forests with lime, oak and hazel (4)), b) broad-leave–coniferous forests (broad-herb spruce–broad-leave forests (5)), and c) broad-leave forests (broad-herb oak forests (6), broad-herb lime forests (7)). In the row of discussed syntaxa from 1 to 7 group, the change in the ratio of coniferous and broad-leave species of the tree layer (A) reflects re­gular decrease in the participation of spruce in the plant cover (from 66 to 6 %; Fig. 3 A1, A2) and an increase in oak and lime more than threefold (from 15 to 65 %; Fig. 4 a). Nemoral species predominate in the composition of ground layers, the cove­rage of which increases (from 40 to 80 %) in the range from 1 to 7 group, the coverage of the boreal group varies from 55 to 8 % (Fig. 11) while maintaining the presence of these species, even in nemoral lime and oak forests. In forests with equal share of broad-leave and coniferous trees (group 5) the nemoral species predominate in herb layer. In oak forests (group 6) the species of the nitro group are maximally represented, which is natural for oak forests occurring on rich soils, and also having abundant undergrowth of hazel. Practically in all studied groups the presence of both coniferous (in particular, spruce) and broad-leave trees in undergrowth (B) and ground layer (C) were present in equal proportions (Fig. 3). This does not confirm the unambiguity of the enrichment with nemoral species and increase in their cover in complex spruce and pine forests in connection with the climate warming in this region, but rather indicates on natural change of the main tree species in the cenopopulations. Further development of the stand and the formation of coni­ferous or broad-leave communities is conditioned by landscape. It is proved that the distribution of different types of communities is statistically significant due to the relief. According to the results of the analysis of remote information, the distribution areas of coniferous forests with broad-leave species, mixed and broad-leave forest areas for the study region are represented equally. The largest massifs of broad-leave–coniferous forests are located in the central and western parts of the study area, while in the eastern one the broad-leave forests predominate, that is a confirmation of the zonal ecotone (along the Pakhra River: Petrov, Kuzenkova, 1968) from broad-leave–coniferous forests to broad-leave forests.

This paper presents a syntaxonomical revision and statistical determination of diagnostic, constant and dominant species of higher syntaxa of Poland based on releves stored in the Polish Vegetation Database. All the analyses were performed on a data set consisting of 43,686 releves containing 2,853 species of vascular plants, bryophytes, algae and lichenized fungi. The data set was subjected to formalized and hierarchical classification, which revealed 44 classes and 153 alliances. The vegetation of Poland is divided into the classes: <em>Zosteretea marinae</em>, <em>Charetea</em>, <em>Elyno-Seslerietea</em>, <em>Violetea calaminariae</em>, <em>Stellarietea mediae</em>, <em>Cakiletea maritimae</em>, <em>Salicetea herbaceae</em>, <em>Isoëto-Nano-Juncetea</em>, <em>Oxycocco-Sphagnetea</em>, <em>Ammophiletea arenariae</em>, <em>Potametea</em>, <em>Thero-Salicornietea</em>, <em>Carici- Kobresietea</em>, <em>Festuco-Puccinellietea</em>, <em>Erico-Pinetea</em>, <em>Juncetea trifidi</em>, <em>Loiseleurio-Vaccinietea</em>, <em>Lemnetea</em>, <em>Quercetea pubescentis</em>, <em>Littorelletea unifiorae</em>, <em>Koelerio-Corynephoretea</em>, <em>Roso pendulinae-Pinetea mugo</em>, <em>Cymbalario-Parietari- etea</em>, <em>Bidentetea tripartitae</em>, <em>Alnetea glutinosae</em>, <em>Scheuchzerio-Caricetea</em>, <em>Robinietea</em>, <em>Montio-Cardaminetea</em>, <em>Thlaspi- etea rotundifolii</em>, <em>Festuco-Brometea</em>, <em>Salicetea purpureae</em>, <em>Molinio-Arrhenatheretea</em>, <em>Mulgedio-Aconitetea</em>, <em>Carpino- Fagetea</em>, <em>Calluno-Ulicetea</em>, <em>Quercetea robori-petraeae</em>, <em>Vaccinio-Piceetea</em>, <em>Polygono arenastri-Poëtea</em>, <em>Asplenietea trichomanis</em>, <em>Phragmito-Magno-Caricetea</em>, <em>Artemisietea vulgaris</em>, <em>Epilobietea angustifolii</em>, <em>Galio-Urticetea</em>, <em>Rhamno- Prunetea</em>. In order to determine a diagnostic species for allianc sures of fidelity were used. A revised list of vegetation units of Poland is presented.

Studies of surface-water pH and bryophyte assemblages in 440 plots from five peatland regions across northern North America reveal a very distinct, two-fold division into fens with a pH mode at 6.76-7.00, in which <i>Amblystegiaceae</i> are prominent, and bogs with a pH mode at 4.01-4.25, in which <i>Sphagnaceae</i> are dominant. The relevance of the data to past and current views on peatland classification is explored.

Daerah penelitian adalah Cagar Alam Sibolangit yang merupakan bagian dari Tahura (taman hutan raya) di sumatera utara. cagar alam sibolangit ini memiliki luas 85,15 Ha. Tujuan penelitian ini adalah 1)mengetahui bagaimana ciri fisik vegetasi flora yang ada di hutan sibolangit, 2) menganalisis klasifikasi jenis flora yang tumbuh dengan suhu dan ketinggian tempat yang berbeda di hutan sibolangit. Teknik pengumpulan data pada penelitian ini menggunakan metode survey lapangan. Survey lapangan digunakan untuk mendapatkan data valid terkait ciri fisik flora untuk klasifikasi flora tersebut. Hasil penelitian menunjukan bahwa jenis flora yang tumbuh di hutan sibolangit sangat beragam dan diklasifikasikan ke dalam 3 filum yaitu: filum spermatophyta, herydophita, dan byrophita. Ketiga jenis filum ini mendominasi pada ketinggian berbeda. Pada ketinggian 700m – 900m filum yang mendominasi adalah spermatophyta dengan kelas Gymnospermae dan angyospermae, ptherophyta, ricciocarpus sp, lycophyta, pada ketinggian 900m – 1100m didominasi filum pheryophyta dengan kelas Pherophyta dan sphenphyta serta lycophyta, angyospermae, bryophyta, hepatophyta dan pada ketinggian 1100m – 1300m, didominasi filum byrophyta dengan kelas Bryophyta dan hepatophyta serta rthocerophyta (mendominasi), ptheropchyta, sphenophyta, lycophyta, angyosmpermae. Kata kunci : Ketinggian tempat, Klasifikasi flora , Filum, Kelas. AbstractThe research area is Sibolangit Nature Reserve which is part of Tahura (forest park) in north sumatera. sibolangit nature reserve has an area of 85.15 Ha. The objectives of this research are 1) to know how the physical characteristics of flora vegetation present in the sibolangite forest, 2) to analyze the classification of flora species that grow with the temperature and height of different places in the sibolangite forest. Data collection techniques in this study using field survey methods. A field survey was used to obtain valid data related to the physical characteristics of the flora for the classification of the florate. The results showed that the type of flora that grows in the forest sibolangit very diverse. And classified into 3 phyla namely: phylum spermatophyta, herydophita, and byrophita. These three types of phyla dominate at different heights. At the height of 700m - 900m the dominant phylum is spermatophyta with class Gymnospermae and angyospermae, ptherophyta, ricciocarpus sp, lycophyta, at an altitude of 900m - 1100m dominated pheryophyta phyla with class Pherophyta and sphenphyta as well as lycophyta, angyospermae, bryophyta, hepatophyta and at an altitude of 1100m - 1300m , dominated byumhyyta phyla by class Bryophyta and hepatophyta and rthocerophyta (dominate), ptheropchyta, sphenophyta, lycophyta, angyosmpermae.Keywords: Elevation of places, Classification of flora, Phylum, Class.

Bryophytic communities in plateau forests of mature Eucalyptus regnans are distributed according to substrate type and microclimate, whereas those in gully rainforests are more catholic. Objective classification of releves indicated the extent to which groupings are shared between these major topographic sites and the degree to which their distribution is mediated by differences in microclimate. Communities on many substrates in E. regnans forests are either seral to a fern floor 'climax' or exhibit pattern and process cycles of regenerative stability.

Peatland plant communities surrounding small (<200 ha) boreal ponds were characterized by indicator species, water and peat chemistry, and diversity. Peatland–pond complexes are common in boreal Alberta and are found in three different landforms (clay-till plain, outwash plain, and moraine). Pond area and perimeter were larger in the clay-till plain than in other landforms, although not significantly different. Across the three landforms, cluster analysis detected five peatland communities: marshes, wet open fens, dry open fens, treed fens, and bogs. The zonation pattern of communities surrounding the ponds varied at all sites, and there was no typical pattern, except that marshes were always found closest to water. Based on the bryophyte species, most communities are considered moderate-rich fens. Nonmetric multidimensional scaling indicated communities fell along a wet-to-dry gradient and a bare-to-vegetated gradient. Water depth and temperature, peat depth, and peat C/N ratios differed between open and treed peatland communities, and pH was similar in all communities. Alpha and gamma diversity was highest in the treed fen and lowest in the marsh community in both total species and bryophyte species. The total number of plant species, some of which are considered rare, found in all communities was 139.Key words: marsh, fen, bog, classification, vegetation ecology, diversity.

Abstract The occurrence of 13 species belonging to eight complex thalloid genera and six families are reported for Hunan. Conocephalum japonicum (Thunb.) Grolle, C. salebrosum Szweykowski et al. and Dumortiera hirsuta (Sw.) Nees are moderately common in Hunan, Conocephalum conicum (L.) Dumort., Marchantia palaecea Bertol. and M. emarginata Reinw. et al. subsp. tosana (Steph.) Bischler are rather rare, M. polymorpha L., Plagiochasma pterospermum Mass., Reboulia hemisphaerica (L.) Raddi, and Wiesnerella denutata (Mitt.) Steph. are rare and Asterella khasyana (Griff.) Pandé et al., Plagiochasma appendiculatum Lehm. & Lindenb. and Riccia fluitans L. are very rare. Of them the following are new to Hunan: Genus Plagiochasma with two species, P. appendiculatum, P. pterospermum, Riccia fluitans, Marchantia paleacea and Conocephalum salebrosum. The altitudinal ranges of taxa in Hunan are mapped. The distribution, ecology and the classification of taxa into distributional elements, as well as the characters are discussed. Some thalloid hepatic genera, i.e. Conocephalum and Dumortiera include cryptic taxa that pose unsolved taxonomic problems that await further future research.

Underground continuity and fungi diversity of old forest sites Old-growth forests (old stands) and ancient forests (historically old forest sites) in general provide a higher biodiversity (number of species) than comparable younger ones. Thus the forest and forest site history in terms of continuity is fundamental for the biodiversity status. Underground continuity comprises several aspects, each of which impacts the biodiversity: continuity of carbon and nitrogen storage, undisturbed ageing of the ground surface (large terrestrial bryophyte cushions and lichen turfs), uninterrupted soil hydrological processes, continuity of natural processes such as bio- and cryoturbation, continuity of soil development and geological layers as well as underground and above ground structural diversity. We describe two approaches for assessing underground continuity. The first is based on records of indicator fungi species (signal species), and the second considers structural surface components. We show the relation between fungi species indicating forest continuity and total fungi diversity without signal species at plot level (500 m2) considering a continuity index and the classification of a regression tree. Finally we conclude that 1) the conservation of forests with long continuity should be prioritized as the high fungi species diversity of these sites contributes greatly to biodiversity, and 2) the underground diversity should be markedly considered in forest monitoring schemes.

An annotated checklist of the pleurocarpous moss genus Plagiothecium in Eurasia is presented for the first time based on a thorough review of the literature. Data have been compiled from previous relevant works conducted on the genus over more than 70 years and published up to the end of June 2020 for 107 Eurasian countries (and islands). Sectional classification is based on molecular phylogeny of the genus published recently. A total of 41 taxa are reported, including 29 species and 12 infraspecific taxa (nine varieties and three forms) belonging to eight sections. The highest numbers of taxa were found in China (20 taxa), the Russian Federation (20 taxa) and Japan (18 taxa), while the smallest numbers of taxa were recorded in the Middle East, Central Asia and the islands area. Not a single species of Plagiothecium was recorded in 26 regions, whereas P. denticulatum, P. nemorale and P. cavifolium turned out to be the most widespread species in the entire study area. They were recorded in most of the surveyed countries and islands. For each accepted taxon, information on relevant literature, synonyms, distribution within Eurasia and globally are provided. Comments on each taxon, ecological preferences, and notes on doubtful records are also included. Additionally, distribution maps for each recognised taxon are supplied. This checklist can enlighten and foster a better understanding of the distribution, diversity, and ecology of Plagiothecium in Eurasia and provides an incentive for future research on the genus.

The scientific discussion concerning the development of the promising approaches for phyto-diversity conservation and the rational use of plant resources in Russian Federation was held at the Presidium of the Russian Academy of Sciences in December 2019. After the reports of leading scientists from biological institutes, a resolution No. 195 dated December 10, 2019 «Global changes in terrestrial ecosystems of Russia in the 21st century: challenges and opportunities» was adopted. The resolution includes a set of priority scientific aims including the development and application of modern technologies for inventory of the plant communities and the development of vegetation classification in Russia. As a result of the opinion exchange between phytocoenologists from different regions, the Concept of Russian Vegetation Classification was proposed. It is based on the following principles. 1. The use of the ecological-floristic approach and the hierarchy of the main syntaxonomic categories applied for the Classification of Vegetation of Europe. 2. Development of the Russian archive of geobotanical relevés and syntaxa in accordance with international standards and with the remote access functions. 3. Application of strict rules for syntaxon names formulated in the International Code of Phytosociological Nomenclature. The Concept assumes the development of a special program «Russian Vegetation Classification» with the justification of the necessity for targeted funding of the program in Research Institutions and Universities involved for solving this scientific problem on the principle of network collaboration. The final results of this program will be represented in the multi-volume publication «Vegetation of Russia». A shortened version of the Concept (English version was kindly revised by Dr. Andrew Gillison, Center for Biodiversity Management, Cairns, Queensand, Australia) is below. Vegetation classification of Russia Research Program Concept Systematic classification and inventory of plant communities (phytocoenoses) is fundamental to the study and forecasting of contemporary complex processes in the biosphere, controlled among other factors, by global climate change. Vegetation classification serves as a common language that enables professionals in various fields of science to communicate and interact with each other in the process of studying and formulating practical ecosystem-related management decisions. Because plant community types can carry a great deal of information about the environment, nearly all approaches to simulation of changes in global biota are based inevitably on vegetation categories. Phytocoenosis is a keystone element when assessing the biodiversity genetic potential, formulating decisions in biological resource management and in sustaining development across Russian territories. Among the world’s vegetation classification systems, phytosociology is a system in which the concept of plant association (basic syntaxon) is the basic element in the classification of phytocoenoses. The phytosociological approach as applied in this concept proposal, has its origins in the Brussels Botanical Congress in 1910. However, despite the broad acceptance of phytocoenotic diversity as a fundamental methodological tool for understanding biosphere processes and managing biological resources nowadays, we still lack a unified approach as to its systematization at both global and country levels with the consequence that, there is no a single classification system. The results obtained by vegetation scientists working under European Vegetation Survey led by L. Mucina became the effective reference for international cooperation in vegetation classification. In the last 17 years they have produced a system of vegetation classification of Europe, including the European part of Russia (Mucina et al., 2016. «Vegetation of Europe: hierarchical floristic classification system of vascular plant, bryophyte, lichen, and algal communities»). Despite the fact that «Vegetation of Europe» is based on ecological and floristic principles, it nevertheless represents an example of the synthesis of one of the most effective approaches to systematizing vegetation diversity by different vegetation science schools. The synthetic approach implemented in this study assumes full accounting of the ecological indicative significance of the floristic composition and structure of plant community and habitat attributes. The approach has already demonstrated its high efficiency for understanding and forecast modeling both natural and anthropogenic processes in the biosphere, as well as in assessment of the environmental and resource significance of vegetation (ref). The demand for this approach is supported by its implementation in a number of pan-European and national projects: NATURE 2000, CORINE, CarHAB, funded at the state and pan-European levels. Currently, one of the main systems for the study and protection of habitats within the framework of environmental programs of the European Union (Davies, Moss, 1999; Rodwell et al., 2002; Moss, 2008; Linking..., 2015; Evans et al., 2018) is EUNIS (European Nature Information System), the framework of which is a multilevel classification of habitats in Europe has been established. EUNIS was used as the basis for the preparation and establishment of the Red List of European Habitats (Rodwell et al., 2013). It is approved by the Commission of the European Union (EU) (Habitats Directive 92/43 / EEC, Commission of the European Communities) for use in environmental activities of EU countries. In its Resolution of 10.12.2019, the Presidium of the Russian Academy of Sciences (RAS) expressed the need in a modern vegetation classification for the assessment of the ecosystem transformations under current climate changes and increasing anthropogenic impacts, as well as in development of effective measures for the conservation and rational use of plant resources of Russia. The resolution recommended the development of the Concept of Vegetation Classification of Russia to the Science Council for biodiversity and biological resources (at RAS Department of biological sciences — Section of Botany). As a consequence, a group of Russian vegetation researchers has developed the Concept for Vegetation Classification of Russia and proposed principles and a plan for its implementation. Aim Elaboration of a system of vegetation classification of Russia reflecting the natural patterns of plant communities formation at different spatial and geographical levels and serving as the fundamental basis for predicting biosphere processes, science-based management of bioresources, conservation of biodiversity and, ultimately, rational nature management for planning sustainable development of its territories. Research goals 1. Development of fundamental principles for the classification of vegetation by synthesis of the achievements of Russian and world’s vegetation science. 2. Inventory of plant community diversity in Russia and their systematization at different hierarchical levels. Elaboration and publication of a Prodromus of vegetation of Russia (syntaxon checklist) with an assessment of the correctness of syntaxa, their Nomenclatural validization and bibliography. Preparation and publication of a book series «Vegetation of Russia» with the entire classification system and comprehensive description of all syntaxonomic units. 3. The study of bioclimatic patterns of the phytocoenotic diversity in Russia for predictive modeling of biosphere processes. Assessment of qualitative changes in plant cover under global climate change and increasing anthropogenic impact in its various forms. 4. Assessment of the conservation value of plant communities and ecosystems. Habitat classification within Russia on the basis of the vegetation classification with a reference to world experience. 5. Demonstration of the opportunities of the vegetation classification for the assessment of actual plant resources, their future prognoses under climate and resource use change, optimization of nature management, environmental engineering and planning of projects for sustainable development. Basic principles underlying the vegetation classification of Russia I. Here we address the synthesis of accumulated theoretical ideas about the patterns of vegetation diversity and the significant features of phytocoenoses. The main goal is to identify the most significant attributes of the plant cover at different hierarchical levels of classification: floristic, structural-phytocoenotic, ecotopic and geographical.We propose the following hierarchy of the main syntaxonomical categories used in the classification of European vegetation (Mucina et al., 2016) by the ecological-floristic approach (Braun-Blanquet): Type of vegetation, Class, Order, Alliance, Association. Applying the ecological-floristic approach to the vegetation classification of Russia will maximize the use of the indicative potential of the plant community species composition to help solve the complex tasks of modern ecology, notably plant resource management, biodiversity conservation, and the forecast of vegetation response to environmental change of environment changes. II. We plan to establish an all-Russian archive of geobotanical relevés in accordance with international standards and reference information system on the syntaxonomical diversity coupled with implemented remote access capabilities. At present, the archives in botanical, biological, environmental and geographical institutes of the Russian Academy of Sciences, as well as those of universities, have accumulated a large mass of geobotanical relevés for most regions of Russia (according to preliminary estimates — more than 300,000). These documents, which are fundamental to solving the most important national tasks for the conservation and monitoring of the natural human environment, need to be declared a National treasure. In this respect, the development of the all-Russian Internet portal for the vegetation classification is an urgent priority. III. The vegetation classification procedure will be based on a generalization of field data (geobotanical relevés) performed in accordance with international standards, using up-to-date mathematical and statistical methods and information technology. IV. The vegetation classification of Russia will be based on strict rules for naming of syntaxa, according to their validity as formulated in the International Code of Phytosociological Nomenclature, which is constantly being improved (Weber et al., 2020). These underlying principles will help develop the ecological indicative potential of a wide range of vegetation features that can be used to focus on solving a range of global and regional ecology problems, plant resources management, biodiversity protection, and forecasting of the consequences of environmental changes. Prospects for the implementation of the concept «Vegetation classification of Russia» At present, the academic research centers and universities of Moscow, St. Petersburg, Novosibirsk, Vladivostok, Irkutsk, Murmansk, Crimea, Bashkiria, Komi and other regions have sufficient scientific potential to achieve the goals in the framework of the special Program of the Russian Academy of Sciences — that is, to develop a vegetation classification of Russia. To achieve this goal will require: - organization of a network of leading teams within the framework of the Scientific Program of the Russian Academy of Sciences «Vegetation classification of Russia», adjustment of the content of state assignment with the allocation of additional funding. - approval of the thematic Program Committee by the RAS for the development of organizational approaches and elaboration of specific plans for the realization of the Scientific Program, - implementation of the zonal-geographical principle in organization of activity on developing the regional classifications and integrating them into a single classification system of the vegetation of Russia. - ensuring the integration of the system of vegetation classification of Russia with similar systems in the countries of the former USSR, Europe, USA, China, Japan, etc. Potential organizations-participants in the scientific Program — 18 institutes of the Russian Academy of Sciences and 8 Universities. Estimated timelines of the implementation of the concept «Vegetation classification of Russia» — 2021–2030. General schedule for the entire period of research 2021. Approval of classification principles, unified methodical and methodological approaches by project participants. Discussion and elaboration of the rules of organization of the all-Russian archive of geobotanical relevés and syntaxa. 2022–2026. Formation of all-Russian archive of geobotanical relevés and syntaxa. Development of plant community classification and identification of the potential indicative features of units of different ranks based on quantitative methods and comparative syntaxonomic analysis with existing classification systems in Europe, North and East Asia. Justification of new concepts for key syntaxa. The study of environmental and geographical patterns of the vegetation diversity in Russia using up-to-date methods of ordination modeling and botany-geography ana­lysis. 2022. Publication of a Prodromus of vegetation classification of Russia. Schedule for the publication of volumes of the «Vegetation classification of Russia» 2023. «Boreal forests and pre-tundra woodlands» 2024. «Forests of the temperate zone» 2025. «Tundra and polar deserts» and «Alpine ve­getation» 2026. «Steppe vegetation» and «Meadow vegetation» 2027. «Aquatic and bog vegetation» 2028. «Halophytic vegetation» 2029. «Synanthropic vegetation» 2027–2030. Development of criteria for assessing the environmental significance of the plant community syntaxonomic categories for various natural zones based on world criteria. Preparation of the volume «Classification of habitats of Russia and assessment of their environmental significance».

Zonal tundra vegetation occupies slightly sloped watershed surfaces, weakly convex tops and gentle slopes of moraine hills and ridges with moderate snow cover and loamy soils (plakors). Environmental conditions of such sites are most relevant to macroclimate (Aleksandrova, 1971; Matveyeva, 1998). For the East European sector of the Arctic this vegetation was described in 30–70 years of last century by the Soviet geobotanists V. D. Aleksandrova (1956), ­ V. N. Andreyev (1932), I. D. Bogdanovskaya-Giye­nef (1938), A. A. Dedov (2006), A. E. Katenin (1972), Z. N. Smirnova (1938), who, following the dominant approach, attributed the described associations mainly to the moss vegetation type. In the Asian sector of the Arctic (Yamal and Taymyr peninsulas, Arctic Yakutia, Wrangel Isl.) and in Alaska some associations of zonal communities with Carex bigelowii s. str., C. bigelowii subsp. arctisibi­rica and C. lugens have been described according to Braun-Blanquet approach: Carici arctisibiricae–Hylocomietum alaskani Matveyeva 1994, Dryado integrifoliae–Caricetum bigelowii Walker et al. 1994, Salici polaris–Hylocomietum alaskani Matveyeva 1998, Carici lugentis–Hylocomietum alaskani Sekretareva 1998 ex Kholod 2007, Salici polaris–Sanionietum uncinatae Kholod 2007, Tephrosero atropurpureae–Vaccinietum vitis-idaeae Telyatnikov et Pristyazhnyuk 2012, Festuco brachyphyllae–Hylocomietum alaskani Lashchinskiy ex Telyatnikov et al. 2014. Our study area in the East European tundras (730 km of south–north and 550 km of west–east directions) covers 3 tundra subzones (arctic, typical and southern) and two floristic subprovinces (Kanin-Pechora and Ural-Novaya Zemlya) (Fig. 1). 7 associations (one with 5 subassociations) based upon 101 authors’ relevés as well 95 ones by geobotanists-predecessors were described or validated on plakors and habitats close to these. Zonal communities are comprised by thick multi-species moss layer formed by mesophylous bryophytes (Aulacomnium turgidum, Hylocomium splendens, Ptilidium ciliare, Racomitrium lanuginosum and Tomentypnum nitens), the presence of Carex bigelowii subsp. arctisibirica, Deschampsia borealis or D. glauca in the herb layer, the high abundance of dwarf-shrubs, the presence, but not always, of Dryas octopetala and shrubby willows. Their plant cover is closed or discontinuous with frost-boils (3-component module of patch of bare ground – rim – trough or 2-component one of flat surface – patches of bare ground — see Fig. 2, 3). Zonal syntaxa are the richest in species number, compare to all others because the placor habitats are moderate in such important environmental characters as moisture and nutrition of soil and snow depth. That’s why they contain, with the same constancy and sometimes abundance, some character species of alliances and classes of intrazonal vegetation: Kobresio-Dryadion Nordh. 1943 (dryad fell-fields on well drained snowless or poor snowy habitats with slightly carbonated loamy-gravelly soils at outcrops of bedrock) and Carici rupestris–Kobresietea bellardii Ohba 1974, Loiseleurio-Arctostaphylion Kalliola ex Nordhagen 1943 (dwarf-shrub and dwarf-shrub-lichen (often with Betula nana) communities on sandy soils) and Loiseleurio procumbentis–Vaccinietea Eggler ex Schubert 1960, Rubo chamaemori–Dicranion elongati Lavrinenko et Lavrinenko 2015 (dwarf-shrub-cloudberry-moss (Dicranum elongatum, Polytrichum strictum)-lichen communities of oligotrophic palsa and polygon peatlands) and Oxycocco-Sphagnetea Br.-Bl. et Tx. ex Westhoff et al. 1946. The basic syntaxon, whose communities occupy the placor habitats in the arctic tundra subzone (southern­ variant) is Salici polaris–Polytrichetum juniperini Aleksandrova 1956, described on the Southern Island of Novaya Zemlya (Table 1). Similar syntaxa in the typical tundra subzone are Carici arctisibiricae–Hylocomietum splendentis Andreyev 1932 nom. mut. propos. hoc loco (Table 5, Fig. 14–17) and Dryado octopetalae–Hylocomietum splendentis Andreyev 1932 nom. mut. propos. hoc loco salicetosum nummulariae (Bogdanov­skaya-Giyenef 1938) subass. nov. (stat. nov.), nom. corr. hoc loco, described by us and earlier by I. D. Bogdanov­skaya-Giyenef (1938) and Z. N. Smirnova (1938) on the Kolguyev Isl. (Table 2, Fig. 3, 5, 6); D. o.–H. s. caricetosum redowskianae subass. nov. hoc loco and D. o.–H. s. caricetosum arctisibiricae (Koroleva et Kulyugina in Chytrý et al. 2015) subass. nov. (stat. nov.) hoc loco (Table 4, Fig. 4, 9–13) — in the most eastern part of the studied area (Vaygach Isl., Yugorskiy Peninsula and Pay-Khoy Range); D. o.–H. s. typicum subass. nov. hoc loco (Tab­le 3), described by us with use the V. N. Andreyev (1932) relevés on Vangureymusyur Upland (Bolshezemelskaya tundra). In the southern tundra subzone the basic zonal association is Calamagrostio lapponicae–Hylocomietum splenden­tis ass. nov. hoc loco (Table 6, Fig. 20–22). Even small deviations from placor habitat conditions are reflected in the community species composition. In such habitats the following syntaxa are described: Deschampsio borealis–Limprichtietum revolventis Aleksandrova 1956 nom. mut. propos. hoc loco and Flavocet­rario nivalis–Dryadetum octopetalae Aleksandrova 1956 nom. mut. propos. hoc loco on gentle slopes and loamy soils, not in moderate soil moisture, but in wet or, on the contrary, well-drained ecotopes on the Novaya Zemlya (Table 1); Dryado octopetalae–Hylocomietum splendentis caricetosum capillaris subass. nov. hoc loco — on the deluvial tails, in the mid and lower parts of the gentle slopes in Bolshezemelskaya and Malozemelskaya tundras (Table 4, Fig. 2, 7, 8); Oxytropido sordidae–Hylocomietum splendentis ass. nov. hoc loco — in the Pakhancheskaya Bay area (the northern part of the Bolshezemelskaya tundra) on strongly sloping well drained slopes (Table 6, Fig. 18, 19). We attributed these syntaxa to zonal vegetation due to the presence of such taxa of its differential combination as shrub Salix glauca, dwarf-shrub Salix polaris, herbs Bistorta major, Carex bigelowii subsp. arctisibirica, Deschampsia borealis, D. glauca, Eriophorum brachyantherum, Juncus biglumis, Luzula arcuata, Pedicularis lapponica, Petasites frigidus, Poa arctica, Saxifraga hieracifolia, S. hirculus, Stellaria peduncularis, Valeriana capitata, mosses Aulacomnium turgidum, Hylocomium splendens, Ptilidium ciliare, Racomitrium lanuginosum, Tomentypnum nitens and lichens Lobaria linita, Nephroma expallidum, Protopannaria pezizoides, Psoroma hypnorum. This combination of taxa differentiates (by the presence, constancy, abundance) the zonal communities in studied area from vegetation of other classes (Carici rupestris–Kobresietea bellardii, Loiseleurio procumbentis–Vaccinietea, Oxycocco-Sphagnetea) (Table 7). The borders of many species area distribution are held in the East European tundras, so the variation of the community species composition along the latitudinal and longitude gradients is quite natural. Thus, in zonal communities Ledum palustre subsp. decumbens and Salix phylicifolia occur and Betula nana as well as hypoarctic dwarf-shrubs Arctous alpina, Empetrum hermaphroditum, Vaccinium uliginosum subsp. microphyllum­ and V. vitis-idaea subsp. minus are most active only in the southern tundra subzone; Salix polaris (its activity increases to the north) and, in some syntaxa, Dryas octopetala are common in the subzones of typical and arctic tundras. In zonal conditions shrubs Salix glauca, Betula nana (prostrate) and all hypoarctic dwarf-shrubs occur in the typical tundra subzone on the mainland and on Kolguyev Isl., while in the northern part of this subzone on Vaygach Isl. they are already absent, ­except the Vaccinium spp. (with low constancy). In the arctic tundra subzone there are no shrubs and hypoarctic dwarf-shrubs on plakors, while Salix polaris is abundant. We believe that these floristic differences of zonal communities can be considered as markers of their subzonal affiliation. A similar shift in species distribution on the latitudinal gradient is established (Matveyeva, 1998) for the zonal biotopes on Taymyr Peninsula. Some species (Arctagrostis latifolia, Cerastium regelii subsp. caespitosum, Saxifraga oppositifolia, Silene acaulis) have high constancy in zonal communities within the Ural-Novaya Zemlya subprovince, as opposed to the Kanin-Pechora one. Herbs Oxyria digyna, Papaver polare, Parrya nudicaulis, Pedicularis sudetica subsp. arctoeuropaea, Saxifraga cernua and S. cespitosa occur with high constancy only in zonal communities on Novaya Zemlya that brings them closer to syntaxa described in the arctic and typical tundra subzones on Taymyr Peninsula (Matveyeva, 1994, 1998). Already in 1994, N. V. Matveyeva stated the need to describe a new class for zonal vegetation. The name Carici arctisibiricae–Hylocomietea alaskani cl. prov. has been reserved for this class in Yalta’s conference on the classification of Russian vegetation (Lavrinenko et al., 2016), Prague’s “Circumpolar Arctic Vegetation Archive and Classification Workshop” (presentation by N. V. Matveyeva) and “Arctic Science Summit Week 2017” (Lavrinenko et al., 2017). We do not attribute the newly described syntaxa to alliance Dryado octopetalae–Caricion arctisibiricae Koroleva et Kulyugina in Chytrý et al. 2015, which was described at the base of 15 relevés by geobotanists-predecessors (V. N. Andreyev, A. A. Dedov) and as well the 11 ones by E. E. Kulyugina for zonal habitats in the East European tundras (Koroleva, Kulyugina, 2015). At least, it is necessary to revise this alliance, since the name of ass. Pediculari oederi–Dryadetum octopetalae (Andreev 1932) Koroleva et Kulyugina 2015 are not legitimate (nomen superfluum), ass. Salici reticulatae–Dryadetum octopetalae Koroleva et Kulyugina 2015 need to be revised and the rank of the third one (Dryado octopetalae–Caricetum arctisibiricae Koroleva et Kulyugina in Chytrý et al. 2015 was lowered by us (in this paper) to subass. Dryado octopetalae–Hylocomietum splendentis caricetosum arctisibiricae; the definitions of both vegetation and habitats are not quite appropriate to the nature reality; diagnostic species were selected randomly. The current position of this alliance within the Carici rupestris–Kobresietea bellardii is debatable, because this makes vague the syntaxonomical content and expands the syntaxonomical boundaries of class whose communities occur in the intrazonal habitats (fell-fields and dwarf-scrub graminoid stands on base-rich substrates). New higher units of zonal vegetation with sedges Carex bigelowii subsp. arctisibirica, C. bige­lowii s. str. and C. lugens, and, most likely, with cotton grass Eriophorum vaginatum, need to be described in the near future, since the data for this are available from various sectors of the Arctic.

The relative contribution of bryophytes to plant diversity, primary productivity, and ecosystem functioning increases towards colder climates. Bryophytes respond to environmental changes at the species level, but because bryophyte species are relatively difficult to identify, they are often lumped into one functional group. Consequently, bryophyte function remains poorly resolved. Here, we explore how higher resolution of bryophyte functional diversity can be encouraged and implemented in tundra ecological studies.
 We briefly review previous bryophyte functional classifications and the roles of bryophytes in tundra ecosystems and their susceptibility to environmental change. Based on shoot morphology and colony organization, we then propose twelve easily distinguishable bryophyte functional groups. To illustrate how bryophyte functional groups can help elucidate variation in bryophyte effects and responses, we compiled existing data on water holding capacity, a key bryophyte trait. Although plant functional groups, can mask potentially high inter- and intraspecific variability, we found better separation of bryophyte functional group means compared to previous grouping systems regarding water holding capacity. This suggests that our bryophyte functional groups truly represent variation in the functional roles of bryophytes in tundra ecosystems. Lastly, we provide recommendations to improve monitoring of bryophyte community changes in tundra study sites.

AbstractChanges in composition and structure of alpine and subalpine plant communities in relation to ecological factors were analysed in the Nízke Tatry Mts, Slovakia. Species cover values of vascular and non-vascular plants in each vegetation plot were recorded on the nine-degree scale. A data set of 156 relevés of alpine and subalpine vegetation was sampled recently during one year in the eastern part of the Nízke Tatry National Park. The data set was analysed by cluster analysis and Detrended Correspondence Analysis. analyses were carried out on the entire data set, including the subset of short grassland and dwarf-shrub vegetation. Major gradients and clusters were ecologically interpreted using Ellenberg indicator values. In the entire data set, the major gradient in species composition was associated with nutrient availability and the second most important gradient with light. In the case of short grassland and dwarf-shrub vegetation, the gradients were different. The first one was associated with soil reaction and the second gradient was associated with moisture. Clusters proposed by numerical classification reproduced many traditional phytosociological associations, namely Seslerietum distichae, Sphagno capillifolii-Empetretum nigri, Junco trifidi-Callunetum vulgaris, Juncetum trifidi, Dryopterido dilatatae-Pinetum mugo, Luzuletum obscurae, Agrostio pyrenaiceae-Nardetum strictae, while some other associations were less clearly differentiated (communities of the alliances Calamagrostion villosae, Adenostylion alliariae, Trisetion fusci, Cratoneuro filicini-Calthion laetae or Salicion herbaceae). The next clusters included Vaccinium and Festuca supina dominated communities and artificial roadside grasslands sown 50 years ago. Bryophytes and lichens were highly represented among diagnostic species of particular associations. Distribution pattern of particular plant communities was strongly influenced by site position either on northern or southern slope of the mountains.

The World Flora Online (WFO) is the collaborative, international initiative to achieve Target 1 of the Global Strategy for Plant Conservation (GSPC): "An online flora of all known plants." WFO provides an open-access, web-based compendium of the world’s plant species, which builds upon existing knowledge and published floras, checklists and revisions but will also require the collection and generation of new information on poorly known groups and unexplored regions (Borsch et al. 2020). The construction of the WFO Taxonomic Backbone is central to the entire WFO as it determines the accessibility of additional content data and at the same time, represents a taxonomic opinion on the circumscription of those taxa. The Plant List v.1.1 (TPL 2013) was the starting point for the backbone, as this was the most comprehensive resource covering all plants available. We have since curated the higher taxonomy of the backbone, based on the following published community-derived classifications: the Angiosperm Phylogeny Group (APG IV 2016), the Pteridophyte Phylogeny Group (PPG I 2016), Bryophytes (Buck et al. 2008), and Hornworts & Liverworts (Söderström et al. 2016). The WFO presents a community-supported consensus classification with the aim of being the authoritative global source of information on the world's plant diversity. The backbone is actively curated by our Taxonomic Expert Networks (TEN), consisting of specialists of taxonomic groups, ideally at the Family or Order level. There are currently 37 approved TENs, involving more than 280 specialists, working with the WFO. There are small TENs like the Begonia Resource Center and the Meconopsis Group (with five specialists), medium TENs like Ericaceae and Zingiberaceae Resource Centers or SolanaceaSource.org (around 15 experts), and larger TENs like Caryophyllales.org and the Legume Phylogeny Working Group, with more than 80 specialists involved. When we do not have taxonomic oversight, the World Checklist of Vascular Plants (WCVP 2019) has been used to update those families from the TPL 2013 classification. Full credit and acknowledgement given to the original sources is a key requirement of this collaborative project, allowing users to refer to the primary data. For example, an association with the original content is kept through the local identifiers used by the taxonomic content providers as a link to their own resources. A key requirement for the WFO Taxonomic Backbone is that every name should have a globally unique identifier that is maintained, ideally forever. After considering several options, the WFO Technology Working Group recommended that the WFO Council establish a WFO Identifier (WFO-ID), a 10-digit number with a “wfo-” prefix, aimed at establishing a resolvable identifier for all existing plant names, which will not only be used in the context of WFO but can be universally used to reference plant names. Management of the WFO Taxonomic Backbone has been a challenge as TPL v1.1 was derived from multiple taxonomic datasets, which led to duplication of records. For that reason, names can be excluded from the public portal by the WFO Taxonomic Working Group or the TENs, but not deleted. A WFO-ID is not deleted nor reused after it has been excluded from the WFO Taxonomic Backbone. Keeping these allows for better matching when assigning WFO-IDs to data derived from content providers. Nevertheless, this implies certain considerations for new names and duplications. New names are added to the WFO Taxonomic Backbone via nomenclators like the International Plants Name Index (IPNI, The Royal Botanic Gardens, Kew et al. 2021) for Angiosperms, and Tropicos (Missouri Botanical Garden 2021) for Bryophytes, as well as harvesting endemic and infraspecific names from Flora providers when providing descriptive content. New names are passed to the TEN to make a judgement on their taxonomic status. When TENs provide a new authoritative taxonomic list for their group, we first produce a Name Matching report to ensure no names are missed. Several issues come from managing and maintaining taxonomic lists, but the process of curating an ever-growing integrated resource leads to an increase in the challenges we face with homonyms, non-standard author abbreviations, orthographic variants and duplicate names when Name Matching. The eMonocot database application, provided by Royal Botanic Gardens, Kew, (Santarsiero et al. 2013) and subsequently adapted by the Missouri Botanical Garden to provide the underlying functionality for WFO's current toolset, has also proven itself to be a challenging component to update. In this presentation, we will share our hands-on experience, technical solutions and workflows creating and maintaining the WFO Taxonomic Backbone.