Global gradients in moss and vascular plant diversity

Knowledge on the distribution and hotspots of different taxon groups is indispensable for improving the state of biodiversity protection. Our aim was to determine if the relations between major environmental factors and species richness of two plant groups, mosses and vascular plants differ on a global scale. The dependence of species richness on environmental factors in 50 regions, covering 17 % of the global terrestrial territory, was analysed with SAS statistical software. Species richness of vascular plants increases significantly towards the equator, but for mosses the increase is not significant. Species richness of mosses and vascular plants are significantly positively correlated only in the near equator zone. Although there were similarities in the trends of mosses and vascular plant diversities at a global scale, their relations with some factors differ with distance from the equator. The effect of precipitation on species richness is similar for both plant groups, but coastline length has a significant positive influence only on moss richness, whereas species richness of vascular plants was related strongly to area and energy input. Therefore, effective conservation policy at both local and global scale demands consideration of all diversity drivers of different taxon groups.     

Bryophyte vegetation in a wooded meadow: relationships with phanerogam diversity and responses to fertilisation

In the Laelatu wooded meadow in Estonia, famous for its phanerogam diversity, the bryophyte community has been investigated in order to compare its flora and diversity relationships with those of the vascular plant community. Ninety-six bryophyte species were found, 13 of them are hepatics; the majority of the bryophytes are epigeic species common to meadows and forests, including many calciphilous species. Vascular plants and bryophytes display opposite responses to fertilisation. For vascular plants, fertilisation increases the coverage and diminishes the number of species, while for bryophytes it diminishes coverage and increases the number of species. The relationship between the number of species in small plots and the total number of species in the area is similar for vascular plants and bryophytes. No significant changes in the bryophyte community in Laelatu wooded meadow has been detected during the last 30 years.     

Bryophyte and vascular plant species richness in boreo-nemoral moist forests and mires

We compare species richness of bryophytes and vascular plants in Estonian moist forests and mires. The material was collected from two wetland nature reserves. Bryophyte and vascular plant species were recorded in 338 homogeneous stands of approximately 1 ha in nine forest and two mire types. Regional species pools for bryophytes and vascular plants were significantly correlated. The correlations between the species richnesses of bryophytes and vascular plants per stand were positive in all community types. The relative richnesses (local richness divided by the regional species pool size) were similar for bryophyte species and for vascular plant species. This shows that on larger scales, conservation of the communities rich in species of one taxonomic plant group, maintains also the species richness of the other. The minimum number of stands needed for the maintenance of the regional species pool of typical species for the every community type was calculated using the species richness accumulation curves. Less stands are needed to maintain the bryophyte species pools (300–5300 for bryophytes and 400–35 000 for vascular plants).     

Vascular plant and bryophytes species representation in the protected areas network on the national scale

The complexity of nature conservation raises questions about biodiversity protection at the level of species as well as their spatial distribution between differently designated nature conservation areas. We have concentrated on comparison of the existing protected areas and recently established conservation initiative areas—Important Plant Areas. We have estimated how well these areas support the protection of two plant groups—bryophytes and vascular plants. We sought answers to the following questions: (a) are there any trends in the distribution of protected bryophyte and vascular plant species in the protected areas network, and (b) does the Important Plant Areas network promote better protection of bryophyte species compared with the existing protected areas network. Our results demonstrated that bryophytes need special care in nature conservation decisions to reach the reasonable conservation target. Important Plant Areas that were targeted to vascular plants have less importance in preserving bryophyte diversity than already existing conservation areas system. Conservation programs like IBA, IPA etc. have their specific tool and outcome to add conservation values to the existing protected areas system.     

Dispersal limitations and historical factors determine the biogeography of specialized terrestrial protists

Recent studies show that soil eukaryotic diversity is immense and dominated by micro‐organisms. However, it is unclear to what extent the processes that shape the distribution of diversity in plants and animals also apply to micro‐organisms. Major diversification events in multicellular organisms have often been attributed to long‐term climatic and geological processes, but the impact of such processes on protist diversity has received much less attention as their distribution has often been believed to be largely cosmopolitan. Here, we quantified phylogeographical patterns in Hyalosphenia papilio, a large testate amoeba restricted to Holarctic Sphagnum‐dominated peatlands, to test if the current distribution of its genetic diversity can be explained by historical factors or by the current distribution of suitable habitats. Phylogenetic diversity was higher in Western North America, corresponding to the inferred geographical origin of the H. papilio complex, and was lower in Eurasia despite extensive suitable habitats. These results suggest that patterns of phylogenetic diversity and distribution can be explained by the history of Holarctic Sphagnum peatland range expansions and contractions in response to Quaternary glaciations that promoted cladogenetic range evolution, rather than the contemporary distribution of suitable habitats. Species distributions were positively correlated with climatic niche breadth, suggesting that climatic tolerance is key to dispersal ability in H. papilio. This implies that, at least for large and specialized terrestrial micro‐organisms, propagule dispersal is slow enough that historical processes may contribute to their diversification and phylogeographical patterns and may partly explain their very high overall diversity.     

Diversity of bryophyte vegetation in some forest types in Estonia: a comparison of old unmanaged and managed forests

The bryophyte vegetation of 3 pairs of unmanaged and managed forest stands, representing Oxalis drained peatland, Aegopodium and Oxalis forest site type, were compared. The total number of bryophyte species in unmanaged stands was 74 and that in managed stands 54. Out of the 20 species occurring only in unmanaged forests, 9 grow on decaying wood, and 3 on trunks or bases of big trees; 13 of them were hepatics. In unmanaged forests 11 hemerophobic species were recorded altogether. Although the difference in substrate and species diversity between unmanaged and managed stands is not statistically significant, in unmanaged forests more substrates characteristic for an old-growth stand are available, and the percentage of species preferring dryer habitats or prolonged humidity is a bit higher than in managed forests; the percentage of species associated with better illuminated habitats is higher in managed forests. Analysis of classification structure of the bryophyte layer synusia shows that the number of societies is also higher in unmanaged forests. This is associated with more numerous microhabitats; the average light and humidity indices calculated for every society, confirm this conclusion. The large discrepancy in bryophyte layer classification structure in old-growth and managed forests of the same forest site type is manifested not so much by species content in synusia as by their abundance proportions. The larger diversity of classification units in unmanaged forests is also seen at the synusia facies level; four of nine facies are confined exclusively to unmanaged stands. This is a strong argument for the informativeness of bryophyte layer classification structure for purposes of indication and monitoring as well.     

Relationships between species richness patterns in deciduous forests at the north Estonian limestone escarpment

Abstract. The flora of the deciduous forests at the base of the north Estonian limestone escarpment is species rich, with an exceptionally high number of rare bryophyte species. Relationships between species richness of bryophyte and herb layers and biotic and environmental conditions were studied, using General Linear Mixed Models. Human disturbance (waste deposit, tree damage etc) was significantly negatively correlated with species richness of both plant layers. Soil nitrogen content was negatively and soil water retention positively correlated with bryophyte species richness, while herb richness was unrelated to soil factors. After eliminating the effects of environment, negative correlations in species richness and cover between the bryophyte and herb layers were discovered on finer scales (1 m²), referring to biotic interactions. This relationship was obscured with the simple correlation analysis. On the other hand, the positive correlation in species pools between the bryophyte and herb layers (0.1 ha) was insignificant. The species pools of both bryophyte and herb layers were significantly positively correlated with the species richness of the tree layer. In summary, bryophyte and herb layer richness responded differently to environmental conditions, but human disturbance significantly decreased the richness of both layers. Due to the uniqueness and small area of these forests we recommend protection and restoration of disturbed sites.     

Methods for monitoring threatened bryophytes

Monitoring is an indispensable tool for assessment of the state of species both locally and globally. The monitoring of bryophyte species has started quite recently and there is need for uniform methods that can be applied in different countries to get comparable results to give a basis for more effective species conservation. Here we present three general monitoring methods that are suitable for all European bryophytes. The method of permanent squares is used for long-lived species inhabiting stable communities on the ground or large rocks. The method of counting separated substrate units is used for species inhabiting tree trunks, boulders or large pieces of decaying wood. The method of sampling is used for short-lived species in unstable communities and for species that are difficult to identify with a hand-lens. The selection of species and sites to be monitored is discussed. Assessment of the current conservational state of the species depends on the state of habitats at monitoring plots that are defined through character and rate of threats, and change of population size compared with previous and first monitoring events. The three monitoring methods are illustrated with examples based on Estonian monitoring experiences. Suggestions of monitoring methods for bryophyte species belonging to the EU Habitat Directive are given.