Global concordance in diversity patterns of vascular plants and terrestrial vertebrates

The factors that determine large-scale patterns of species richness are poorly understood. In particular, biologists have not determined the relative roles of taxon-specific characteristics that influence diversification and distribution, and region-specific features that promote and constrain diversity. We show that the numbers of species of vascular plants and of four terrestrial vertebrate taxa (mammals, birds, reptiles and amphibians) vary in parallel across 296 geographic areas covering most of the globe, even after accounting for sample area, climate, topographic heterogeneity and differences between continents. Thus, a common set of regional characteristics and processes appears to shape patterns of species richness in a diverse set of taxa, despite substantial differences in their biological traits.     

Regional effects as important determinants of local diversity in both marine and terrestrial systems

Community ecologists have struggled to create unified theories across diverse ecosystems, but it has been difficult to acertain whether marine and terrestrial communities differ in the mechanisms responsible for structure and dynamics. One apparent difference between marine and terrestrial ecology is that the influence of regional processes on local populations and communities is better established in the marine literature. We examine three potential explanations: 1) influential early studies emphasized local interactions in terrestrial communities and regional dispersal in marine communities. 2) regional‐scale processes are actually more important in marine than in terrestrial communities. 3) recruitment from a regional species pool is easier to study in marine than terrestrial communities. We conclude that these are interrelated, but that the second and especially the third explanations are more important than the first. We also conclude that in both marine and terrestrial systems, there are ways to improve our understanding of regional influences on local community diversity. In particular, we advocate examining local vs regional diversity relationships at localities within environmentally similar regions that differ in their diversity either because of their sizes or their varying degrees of isolation from a species source.     

Spatial patterns of plant diversity below-ground as revealed by DNA barcoding

Our understanding of the spatial organization of root diversity in plant communities and of the mechanisms of community assembly has been limited by our ability to identify plants based on root tissue, especially in diverse communities. Here, we test the effectiveness of the plastid gene rbcL, a core plant DNA barcoding marker, for investigating spatial patterns of root diversity, and relate observed patterns to above-ground community structure. We collected 3800 root fragments from four randomly positioned, 1-m-deep soil profiles (two vertical transects per plot), located in an old-field community in southern Ontario, Canada, and extracted and sequenced DNA from 1531 subsampled fragments. We identified species by comparing sequences with a DNA barcode reference library developed previously for the local flora. Nearly 85% of sampled root fragments were successfully sequenced and identified as belonging to 29 plant species or species groups. Root abundance and species richness varied in horizontal space and were negatively correlated with soil depth. The relative abundance of taxa below-ground was correlated with their frequency above-ground (r = 0.73, P = 0.0001), but several species detected in root tissue were not observed in above-ground quadrats. Multivariate analyses indicated that diversity was highly structured below-ground, and associated with depth, root morphology, soil chemistry and soil texture, whereas little structure was evident above-ground. Furthermore, analyses of species co-occurrence indicates strong species segregation overall but random co-occurrence among confamilials. Our results provide insights into the role of environmental filtering and competitive interactions in the organization of plant diversity below-ground, and also demonstrate the utility of barcoding for the identification of plant roots.     

Plant diversity surpasses plant functional groups and plant productivity as driver of soil biota in the long term

Background

One of the most significant consequences of contemporary global change is the rapid decline of biodiversity in many ecosystems. Knowledge of the consequences of biodiversity loss in terrestrial ecosystems is largely restricted to single ecosystem functions. Impacts of key plant functional groups on soil biota are considered to be more important than those of plant diversity; however, current knowledge mainly relies on short-term experiments.

Methodology/Principal Findings

We studied changes in the impacts of plant diversity and presence of key functional groups on soil biota by investigating the performance of soil microorganisms and soil fauna two, four and six years after the establishment of model grasslands. The results indicate that temporal changes of plant community effects depend on the trophic affiliation of soil animals: plant diversity effects on decomposers only occurred after six years, changed little in herbivores, but occurred in predators after two years. The results suggest that plant diversity, in terms of species and functional group richness, is the most important plant community property affecting soil biota, exceeding the relevance of plant above- and belowground productivity and the presence of key plant functional groups, i.e. grasses and legumes, with the relevance of the latter decreasing in time.

Conclusions/Significance

Plant diversity effects on biota are not only due to the presence of key plant functional groups or plant productivity highlighting the importance of diverse and high-quality plant derived resources, and supporting the validity of the singular hypothesis for soil biota. Our results demonstrate that in the long term plant diversity essentially drives the performance of soil biota questioning the paradigm that belowground communities are not affected by plant diversity and reinforcing the importance of biodiversity for ecosystem functioning.     

Policies for plant diversity conservation on a global scale: a Nitrogen driver analysis

Diversity is a complex term that includes taxonomic, functional, spatial and temporal aspects of organisms variety. Conservation policies must be supported by holistic studies of ecosystem function, must aim to transform scientific knowledge into social responsibility creating a culture of respect towards nature and should also include economic components. Mediterranean ecosystems will likely experience the greatest proportional changes in biodiversity due to the substantial influence of land use and climate change as major drivers. Land use includes not only rural abandonment but also intensive exploitation of native forests (cork oak woodlands) or shrublands for animal or crop production. These last two are dependent on large Nitrogen (N) inputs. In this paper we intend to show the responses of Mediterranean ecosystems to increased N availability in terms of biodiversity and ecosystem functionality. We present two case studies: 1) a gradient of N availability due to a N point source; and 2) N manipulative field experiment (doses and forms). With these results our aim is to pinpoint the importance of improving scientific knowledge at a local level before we establish conservation policies at global level. The two case studies reflect a strong influence of the N source on ecosystem function. Finally, we use the SWOT (Strengths, Weakness, Opportunities and Threats) analysis approach to underpin the complexities of human intervention in the N cycle and the problem it poses for policies of plant conservation.     

Eco-evolutionary litter feedback as a driver of exotic plant invasion

Many studies have examined positive feedbacks between invasive plant traits and nutrient cycling, but few have investigated whether feedbacks arise from introduction of pre-adapted species or from eco-evolutionary feedback that develops after introduction. Eco-evolutionary feedback could occur between an invader's leaf tissue C:N ratio and its response to litter accumulation. Previous modeling predicts that occurrence of this feedback would be reflected by: (1) field data showing higher litter:biomass ratios in the invasive range; (2) high C:N genotypes benefiting more from experimental litter additions than low C:N genotypes; (3) this beneficial effect on high C:N genotypes inducing a critical transition toward invader dominance when a critical amount of litter is added to a native species-dominated community experiencing low nutrient conditions. Here, we empirically tested these predictions for the invasive grass Phalaris arundinacea, which has undergone post-introduction evolutionary change toward attaining higher C:N ratios under high nutrient conditions. We performed a biogeographical comparison of litter:biomass ratios in the native (Europe) and invasive (USA) range, and an experiment with mesocosms from the invasive range under low nutrient conditions. Low and high C:N Phalaris genotypes were introduced into native-dominated and bare mesocosms, to which varying litter amounts were added. The biogeographical comparison revealed that litter:biomass ratios were higher in the invasive range. The mesocosm experiment showed that when grown in isolation, only high C:N genotypes responded positively to litter. This effect, however, was not strong enough to stimulate Phalaris when exposed to competition with native species. Our results suggest that eco-evolutionary feedback between Phalaris’ C:N ratio and litter accumulation could occur, but only under high nutrient conditions. Our experiments suggest that eco-evolutionary feedback may select for specialist rather than superior genotypes. Hence, genotypic variation induced by post-introduction admixture may be subject to context-dependent selection due to eco-evolutionary feedback, increasing trait variation within invasive populations.     

Exploring the relationship between canopy height and terrestrial plant diversity

A relatively small number of broad-scale patterns describe the distribution of biodiversity across the earth. All of them explore biodiversity focusing on a mono or bi-dimensional space. Conversely, the volume of the forests is rarely considered. In the present work, we tested a global correlation between vascular plant species richness (S) and average forest canopy height (H), the latter regarded as a proxy of volume, using the NASA product of Global Forest Canopy Height map and the global map of plant species diversity. We found a significant correlation between H and S both at global and macro-climate scales, with strongest confidence in the tropics. Hence, two different regression models were compared and discussed to provide a possible pattern of the H–S relation. We suggested that the volume of forest ecosystems should be considered in ecological studies as well as in planning and managing natural sites, although in this first attempt, we cannot definitively prove our hypothesis. Again, high-resolution spatial data could be highly important to confirm the H–S relation, even at different scales.     

Global patterns of plant diversity and floristic knowledge

Aims We present the first global map of vascular plant species richness by ecoregion and compare these results with the published literature on global priorities for plant conservation. In so doing, we assess the state of floristic knowledge across ecoregions as described in floras, checklists, and other published documents and pinpoint geographical gaps in our understanding of the global vascular plant flora. Finally, we explore the relationships between plant species richness by ecoregion and our knowledge of the flora, and between plant richness and the human footprint – a spatially explicit measure of the loss and degradation of natural habitats and ecosystems as a result of human activities. Location Global. Methods Richness estimates for the 867 terrestrial ecoregions of the world were derived from published richness data of c. 1800 geographical units. We applied one of four methods to assess richness, depending on data quality. These included collation and interpretation of published data, use of species–area curves to extrapolate richness, use of taxon‐based data, and estimates derived from other ecoregions within the same biome. Results The highest estimate of plant species richness is in the Borneo lowlands ecoregion (10,000 species) followed by nine ecoregions located in Central and South America with ≥ 8000 species; all are found within the Tropical and Subtropical Moist Broadleaf Forests biome. Among the 51 ecoregions with ≥ 5000 species, only five are located in temperate regions. For 43% of the 867 ecoregions, data quality was considered good or moderate. Among biomes, adequate data are especially lacking for flooded grasslands and flooded savannas. We found a significant correlation between species richness and data quality for only a few biomes, and, in all of these cases, our results indicated that species‐rich ecoregions are better studied than those poor in vascular plants. Similarly, only in a few biomes did we find significant correlations between species richness and the human footprint, all of which were positive. Main conclusions The work presented here sets the stage for comparisons of degree of concordance of plant species richness with plant endemism and vertebrate species richness: important analyses for a comprehensive global biodiversity strategy. We suggest: (1) that current global plant conservation strategies be reviewed to check if they cover the most outstanding examples of regions from each of the world's major biomes, even if these examples are species‐poor compared with other biomes; (2) that flooded grasslands and flooded savannas should become a global priority in collecting and compiling richness data for vascular plants; and (3) that future studies which rely upon species–area calculations do not use a uniform parameter value but instead use values derived separately for subregions.     

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.     

Beech carbon productivity as driver of ectomycorrhizal abundance and diversity

We tested the hypothesis that carbon productivity of beech ( Fagus sylvatica ) controls ectomycorrhizal colonization, diversity and community structures. Carbon productivity was limited by long-term shading or by girdling. The trees were grown in compost soil to avoid nutrient deficiencies. Despite severe limitation in photosynthesis and biomass production by shading, the concentrations of carbohydrates in roots were unaffected by the light level. Shade-acclimated plants were only 10% and sun-acclimated plants were 74% colonized by ectomycorrhiza. EM diversity was higher on roots with high than at roots with low mycorrhizal colonization. Evenness was unaffected by any treatment. Low mycorrhizal colonization had no negative effects on plant mineral nutrition. In girdled plants mycorrhizal colonization and diversity were retained although ¹⁴C-leaf feeding showed almost complete disruption of carbon transport from leaves to roots. Carbohydrate storage pools in roots decreased upon girdling. Our results show that plant carbon productivity was the reason for and not the result of high ectomycorrhizal diversity. We suggest that ectomycorrhiza can be supplied by two carbon routes: recent photosynthate and stored carbohydrates. Storage pools may be important for ectomycorrhizal survival when photoassimilates were unavailable, probably feeding preferentially less carbon demanding EM species as shifts in community composition were found.     

Evolution in plant populations as a driver of ecological changes in arthropod communities

Heritable variation in traits can have wide-ranging impacts on species interactions, but the effects that ongoing evolution has on the temporal ecological dynamics of communities are not well understood. Here, we identify three conditions that, if experimentally satisfied, support the hypothesis that evolution by natural selection can drive ecological changes in communities. These conditions are: (i) a focal population exhibits genetic variation in a trait(s), (ii) there is measurable directional selection on the trait(s), and (iii) the trait(s) under selection affects variation in a community variable(s). When these conditions are met, we expect evolution by natural selection to cause ecological changes in the community. We tested these conditions in a field experiment examining the interactions between a native plant (Oenothera biennis) and its associated arthropod community (more than 90 spp.). Oenothera biennis exhibited genetic variation in several plant traits and there was directional selection on plant biomass, life-history strategy (annual versus biennial reproduction) and herbivore resistance. Genetically based variation in biomass and life-history strategy consistently affected the abundance of common arthropod species, total arthropod abundance and arthropod species richness. Using two modelling approaches, we show that evolution by natural selection in large O. biennis populations is predicted to cause changes in the abundance of individual arthropod species, increases in the total abundance of arthropods and a decline in the number of arthropod species. In small O. biennis populations, genetic drift is predicted to swamp out the effects of selection, making the evolution of plant populations unpredictable. In short, evolution by natural selection can play an important role in affecting the dynamics of communities, but these effects depend on several ecological factors. The framework presented here is general and can be applied to other systems to examine the community-level effects of ongoing evolution.     

Plant species diversity as a driver of early succession in abandoned fields: a multi-site approach

Succession is one of the most studied processes in ecology and succession theory provides strong predictability. However, few attempts have been made to influence the course of succession thereby testing the hypothesis that passing through one stage is essential before entering the next one. At each stage of succession ecosystem processes may be affected by the diversity of species present, but there is little empirical evidence showing that plant species diversity may affect succession. On ex-arable land, a major constraint of vegetation succession is the dominance of perennial early-successional (arable weed) species. Our aim was to change the initial vegetation succession by the direct sowing of later-successional plant species. The hypothesis was tested that a diverse plant species mixture would be more successful in weed suppression than species-poor mixtures. In order to provide a robust test including a wide range of environmental conditions and plant species, experiments were carried out at five sites across Europe. At each site, an identical experiment was set up, albeit that the plant species composition of the sown mixtures differed from site to site. Results of the 2-year study showed that diverse plant species mixtures were more effective at reducing the number of natural colonisers (mainly weeds from the seed bank) than the average low-diversity treatment. However, the effect of the low-diversity treatment depended on the composition of the species mixture. Thus, the effect of enhanced species diversity strongly depended on the species composition of the low-diversity treatments used for comparison. The effects of high-diversity plant species mixtures on weed suppression differed between sites. Low-productivity sites gave the weakest response to the diversity treatments. These differences among sites did not change the general pattern. The present results have implications for understanding biological invasions. It has been hypothesised that alien species are more likely to invade species-poor communities than communities with high diversity. However, our results show that the identity of the local species matters. This may explain, at least partly, controversial results of studies on the relation between local diversity and the probability of being invaded by aliens. Received: 13 July 1999 / Accepted: 4 February 2000     

特有植物多样性分布格局测度方法的新进展

特有植物是生物多样性保护的重要对象,对其分布格局的研究可以为生物多样性优先保护区的确定提供重要参考.研究人员利用多种测度和分析方法,在不同地理区域对特有现象的分布格局开展了大量研究.随着分子系统学方法的不断完善及一些空间统计分析方法的引入,新的生物多样性测度方法应运而生.本文介绍了生物多样性测度方法的类型及其特点、应用现状与前景.这些测度方法的发展经历了从单一的时间或空间格局到时空格局统一的过程,具体涉及物种丰富度、谱系多样性、进化特异性以及这3种测度方法整合空间分布加权的算法.其中,谱系多样性指数(phylogenetic diversity)、谱系特有性指数(phylogenetic endemism)以及空间加权的进化特异性指数(biogeographically weighted evolutionary distinctiveness)尤其值得关注.中国特有植物分布格局的研究需要在以下4个方面进一步开展工作:(1)完善特有物种的分布格局研究;(2)加强物种的测序工作,完善谱系多样性格局的分析;(3)结合系统发育信息,揭示谱系多样性及进化历史的分布格局,进而深入开展物种p多样性和谱系p多样性的研究;(4)加强物种分布区变化的模拟,在时间维度上探讨特有现象的变化格局,为生物多样性保护提供更完善的理论支持.     

Diversity patterns of seasonal wetland plant communities mainly driven by rare terrestrial species

In cleared landscapes, wetlands can represent important reservoirs of native plant diversity, which include terrestrial species. Depending on study aims, non-wetland plants might be removed before analysis, affecting conclusions around biodiversity and community structure. We compared the native plant communities of seasonal wetlands in a predominately agricultural landscape as defined geographically (including all species) with that of the obligate wetland assemblage. We were primarily concerned with determining how this design decision affects ecological and conservation conclusions. We analysed a survey database containing >12,900 flora records from South Australia, developing a new area-based method to remove sampling bias to include only wetlands with a near-complete census. We modelled occupancy, species-area relationships, β-diversity and nestedness under our contrasting community definitions. Terrestrial species were 57.4 % of total richness. Removing these species reduced wetland α-diversity by 45 %, but did not affect the scaling of richness with area (power-law species-area relationship z = 0.21 ± 0.01). Occupancies for wetland plants were relatively uniform, but were heavily dominated by rare (satellite) species when terrestrial plants were included, and this also increased β-diversity. Nestedness for terrestrial species occupancies was marginally lower than predicted under null models, suggesting that rare species often do not co-occur with common species. An implication of these occupancy patterns is that twice as many wetlands (and 50 % more wetland area) would be needed to include every native species within at least one wetland compared with wetland-only species.     

The significance of plant growth-forms as shelter for terrestrial animals

Different plant growth-forms such as tussocks and rosettes, were selected as micro ecosystems in an area in which these structures were spatially isolated from each other. These growth forms are important during winter since they serve to regulate temperatures, which is important to invertebrate animals. This was shown with intensive temperature recordings in winter, correlated with numbers of animals. Plant growth-forms are more important in young bare areas where there are fewer plants to provide shelter, than in older areas, where a denser vegetation cover affords more possibilities for shelter. Such differences can be expected to influence the abundance as well as the occurrence of animals during the development of a community.     

Ecosystem-phase interactions: aquatic eutrophication decreases terrestrial plant diversity in California vernal pools

Eutrophication has long been known to negatively affect aquatic and terrestrial ecosystems worldwide. In freshwater ecosystems, excessive nutrient input results in a shift from vascular plant dominance to algal dominance, while the nutrient-species richness relationship is found to be unimodal. Eutrophication studies are usually conducted in continuously aquatic or terrestrial habitats, but it is unclear how these patterns may be altered by temporal heterogeneity driven by precipitation and temperature variation. The California vernal pool (CVP) ecosystem consists of three distinct phases (aquatic, terrestrial, and dry) caused by variation in climatic conditions. The purpose of this study was to test the hypothesis that resource addition during the aquatic phase results in increased algal abundance, which reduces vascular plant cover and richness of the terrestrial phase upon desiccation. We used mesocosms layered with CVP soil, in which treatments consisted of five levels of nitrogen and phosphorous added every 2 weeks. Resource addition increased available phosphorus levels and algae cover during the aquatic phase. Increased algal crusts resulted in decreased vascular plant percent cover and species richness. Few significant patterns were observed with individual plant species and total biomass. The phosphorus-plant richness relationship was not significant, but species composition was significantly different among the low and high treatment comparisons. These results highlight a neglected effect of eutrophication in seasonal habitats. Interactions among ecosystem phases clearly require more attention empirically and theoretically. Management and restoration of temporally heterogeneous habitat, such as the endemic-rich CVP, need to consider the extensive effects of increased nutrient input.