Water availability drives aboveground biomass and bird richness in forest restoration plantings to achieve carbon and biodiversity cobenefits

To combat global warming and biodiversity loss, we require effective forest restoration that encourages recovery of species diversity and ecosystem function to deliver essential ecosystem services, such as biomass accumulation. Further, understanding how and where to undertake restoration to achieve carbon sequestration and biodiversity conservation would provide an opportunity to finance ecosystem restoration under carbon markets. We surveyed 30 native mixed‐species plantings in subtropical forests and woodlands in Australia and used structural equation modeling to determine vegetation, soil, and climate variables most likely driving aboveground biomass accrual and bird richness and investigate the relationships between plant diversity, aboveground biomass accrual, and bird diversity. We focussed on woodland and forest‐dependent birds, and functional groups at risk of decline (insectivorous, understorey‐nesting, and small‐bodied birds). We found that mean moisture availability strongly limits aboveground biomass accrual and bird richness in restoration plantings, indicating potential synergies in choosing sites for carbon and biodiversity purposes. Counter to theory, woody plant richness was a poor direct predictor of aboveground biomass accrual, but was indirectly related via significant, positive effects of stand density. We also found no direct relationship between aboveground biomass accrual and bird richness, likely because of the strong effects of moisture availability on both variables. Instead, moisture availability and patch size strongly and positively influenced the richness of woodland and forest‐dependent birds. For understorey‐nesting birds, however, shrub cover and patch size predicted richness. Stand age or area of native vegetation surrounding the patch did not influence bird richness. Our results suggest that in subtropical biomes, planting larger patches to higher densities, ideally using a diversity of trees and shrubs (characteristics of ecological plantings) in more mesic locations will enhance the provision of carbon and biodiversity cobenefits. Further, ecological plantings will aid the rapid recovery of woodland and forest bird richness, with comparable aboveground biomass accrual to less diverse forestry plantations.     

Disentangling environmental correlates of vascular plant biodiversity in a Mediterranean hotspot

We determined the environmental correlates of vascular plant biodiversity in the Baetic‐Rifan region, a plant biodiversity hotspot in the western Mediterranean. A catalog of the whole flora of Andalusia and northern Morocco, the region that includes most of the Baetic‐Rifan complex, was compiled using recent comprehensive floristic catalogs. Hierarchical cluster analysis (HCA) and detrended correspondence analysis (DCA) of the different ecoregions of Andalusia and northern Morocco were conducted to determine their floristic affinities. Diversity patterns were studied further by focusing on regional endemic taxa. Endemic and nonendemic alpha diversities were regressed to several environmental variables. Finally, semi‐partial regressions on distance matrices were conducted to extract the respective contributions of climatic, altitudinal, lithological, and geographical distance matrices to beta diversity in endemic and nonendemic taxa. We found that West Rifan plant assemblages had more similarities with Andalusian ecoregions than with other nearby northern Morocco ecoregions. The endemic alpha diversity was explained relatively well by the environmental variables related to summer drought and extreme temperature values. Of all the variables, geographical distance contributed by far the most to spatial turnover in species diversity in the Baetic‐Rifan hotspot. In the Baetic range, climate was the most significant driver of nonendemic species beta diversity, while lithology and climate were the main drivers of endemic beta diversity. Despite the fact that Andalusia and northern Morocco are presently separated by the Atlantic Ocean and the Mediterranean Sea, the Baetic and Rifan mountain ranges have many floristic similarities – especially in their western ranges – due to past migration of species across the Strait of Gibraltar. Climatic variables could be shaping the spatial distribution of endemic species richness throughout the Baetic‐Rifan hotspot. Determinants of spatial turnover in biodiversity in the Baetic‐Rifan hotspot vary in importance between endemic and nonendemic species.     

Roles of Spatial Scale and Rarity on the Relationship between Butterfly Species Richness and Human Density in South Africa

Wildlife and humans tend to prefer the same productive environments, yet high human densities often lead to reduced biodiversity. Species richness is often positively correlated with human population density at broad scales, but this correlation could also be caused by unequal sampling effort leading to higher species tallies in areas of dense human activity. We examined the relationships between butterfly species richness and human population density at five spatial resolutions ranging from 2'' to 60'' across South Africa. We used atlas-type data and spatial interpolation techniques aimed at reducing the effect of unequal spatial sampling. Our results confirm the general positive correlation between total species richness and human population density. Contrary to our expectations, the strength of this positive correlation did not weaken at finer spatial resolutions. The patterns observed using total species richness were driven mostly by common species. The richness of threatened and restricted range species was not correlated to human population density. None of the correlations we examined were particularly strong, with much unexplained variance remaining, suggesting that the overlap between butterflies and humans is not strong compared to other factors not accounted for in our analyses. Special consideration needs to be made regarding conservation goals and variables used when investigating the overlap between species and humans for biodiversity conservation.     

Diversity of European habitat types is correlated with geography more than climate and human pressure

Habitat richness, that is, the diversity of ecosystem types, is a complex, spatially explicit aspect of biodiversity, which is affected by bioclimatic, geographic, and anthropogenic variables. The distribution of habitat types is a key component for understanding broad‐scale biodiversity and for developing conservation strategies. We used data on the distribution of European Union (EU) habitats to answer the following questions: (i) how do bioclimatic, geographic, and anthropogenic variables affect habitat richness? (ii) Which of those factors is the most important? (iii) How do interactions among these variables influence habitat richness and which combinations produce the strongest interactions? The distribution maps of 222 terrestrial habitat types as defined by the Natura 2000 network were used to calculate habitat richness for the 10 km × 10 km EU grid map. We then investigated how environmental variables affect habitat richness, using generalized linear models, generalized additive models, and boosted regression trees. The main factors associated with habitat richness were geographic variables, with negative relationships observed for both latitude and longitude, and a positive relationship for terrain ruggedness. Bioclimatic variables played a secondary role, with habitat richness increasing slightly with annual mean temperature and overall annual precipitation. We also found an interaction between anthropogenic variables, with the combination of increased landscape fragmentation and increased population density strongly decreasing habitat richness. This is the first attempt to disentangle spatial patterns of habitat richness at the continental scale, as a key tool for protecting biodiversity. The number of European habitats is related to geography more than climate and human pressure, reflecting a major component of biogeographical patterns similar to the drivers observed at the species level. The interaction between anthropogenic variables highlights the need for coordinated, continental‐scale management plans for biodiversity conservation.     

­­Cross-taxon congruence in wetlands: Assessing the value of waterbirds as surrogates of macroinvertebrate biodiversity in Mediterranean Ramsar sites

Wetlands are among the most threatened habitats and the species they support among the most endangered taxa. Measuring and monitoring wetland biodiversity is vital for conservation, restoration and management, and often relies on the use of surrogate taxa. Waterbirds are commonly used as flagships of biodiversity and are the subject of major conservation initiatives. Therefore, it is important to assess the extent to which waterbirds indicate the general biodiversity of wetlands and serve as surrogates.We explore the relationships between community composition and species richness of waterbirds and aquatic macroinvertebrates in 36 Ramsar wetlands in southern Spain to assess if waterbirds are good surrogates for other taxonomic groups. Specifically, we aimed to (i) test the congruence of patterns of species composition and richness among waterbirds and aquatic macroinvertebrates; and (ii) investigate which environmental variables are associated with the biodiversity patterns of waterbirds and macroinvertebrates, with the purpose of identifying key factors explaining potential discordance in these patterns.We found a limited concordance between assemblage patterns of both taxonomic groups that may be related to their contrasting responses to environmental gradients. Assemblages of waterbirds appear to be more affected by climate variables and water surface area, whereas conductivity was the most important factor influencing macroinvertebrate communities. Furthermore, we found a negligible or inverse relationship in their patterns of richness, with wetlands with higher waterbird species richness showing significantly lower richness of Hemiptera and macroinvertebrate families, and no significant relationship with Coleoptera. In addition, GLM models showed that, in general, different environmental variables are related with the richness patterns of the different taxonomic groups.Given the importance of the Ramsar convention for the conservation of an international network of wetlands, our findings underline the limited potential of waterbirds as aquatic biodiversity indicators in Mediterranean wetlands, and the need for caution when using waterbirds as flagships. An integrative analysis of different biological communities, using datasets from different taxonomic groups, is a necessary precursor for successful conservation policies and monitoring. Our results illustrate the need to create a diversified and complete network of protected sites able to conserve multiple components of wetland biodiversity.     

Threats and biodiversity in the mediterranean biome

Aim Global conservation assessments recognize the mediterranean biome as a priority for the conservation of the world's biodiversity. To better direct future conservation efforts in the biome, an improved understanding of the location, magnitude and trend of key threats and their relationship with species of conservation importance is needed. Location Mediterranean‐climate regions in California‐Baja California, Chile, South Africa, Australia and the Mediterranean Basin. Methods We undertook a systematic, pan‐regional assessment of threats in the mediterranean biome including human population density, urban area and agriculture. To realize the full implications of these threats on mediterranean biodiversity, we examined their relationship with species of conservation concern: threatened mammals at the global scale and threatened plants at the subecoregional scale in California, USA. Results Across the biome, population density and urban area increased by 13% and agriculture by 1% between 1990 and 2000. Both population density and urban area were greatest in California‐Baja California and least in Australia while, in contrast, agriculture was greatest in Australia and least in California‐Baja California. In all regions lowlands were most affected by the threats analysed, with the exception of population density in the Chilean matorral. Threatened species richness had a significant positive correlation with population density at global and subecoregional scales, while threatened species were found to increase with the amount of urban area and decrease as the amount of natural area and unfragmented core area increased. Main conclusions Threats to mediterranean biodiversity have increased from 1990 to 2000, although patterns vary both across and within the five regions. The need for future conservation efforts is further underlined by the positive correlation between species of conservation concern and the increase in population density over the last decade. Challenges to reducing threats extend beyond those analysed to include human–environmental interactions and their synergistic effects, such as urbanization and invasive species and wildfires.     

The role of transitional areas as avian biodiversity centres

Aim  With the ever-increasing threats to biodiversity, efforts are being directed towards identifying hotspots of special importance for conservation. In particular, there has been an effort to identify irreplaceable regions that are especially rich in rare species. Areas of transition between ecological systems in which multiple species coincide are expected, almost by definition, to be species-rich. Here, we examine whether this is simply a result of an overlap between two communities in boundary regions, or whether boundary areas also hold concentrations of rare (e.g. range-limited) species. We ask whether an analysis that includes areas of transition may be a useful contribution to the identification of biodiversity centres.
Location and methods  To address these questions, we examined the relationship between passeriform richness and range size rarity of approximately 2300 bird species in 4889 1° New World grid cells, and the distance of the cells to boundaries between adjacent plant-based ecoregions.
Results  Areas nearer to boundary regions between ecoregions not only had more bird species, but also scored more highly in terms of species rarity. The range centres of the rarest 10% of species were distributed significantly closer to boundaries between ecoregions than were species in general. This pattern persisted for rarity when we divided the New World into three latitudinal belts and analysed each separately, and when we excluded the Andes. It also persisted when compared with randomly generated ecoregion polygons.
Main conclusions  The findings of this work suggest that transitional environments harbour many rare species, in addition to high richness. Consequently areas of biotic transition should be highly valued as biodiversity centres and need to be included in future global conservation analyses and decisions.     

A climatic stability approach to prioritizing global conservation investments

Climate change is impacting species and ecosystems globally. Many existing templates to identify the most important areas to conserve terrestrial biodiversity at the global scale neglect the future impacts of climate change. Unstable climatic conditions are predicted to undermine conservation investments in the future. This paper presents an approach to developing a resource allocation algorithm for conservation investment that incorporates the ecological stability of ecoregions under climate change. We discover that allocating funds in this way changes the optimal schedule of global investments both spatially and temporally. This allocation reduces the biodiversity loss of terrestrial endemic species from protected areas due to climate change by 22% for the period of 2002-2052, when compared to allocations that do not consider climate change. To maximize the resilience of global biodiversity to climate change we recommend that funding be increased in ecoregions located in the tropics and/or mid-elevation habitats, where climatic conditions are predicted to remain relatively stable. Accounting for the ecological stability of ecoregions provides a realistic approach to incorporating climate change into global conservation planning, with potential to save more species from extinction in the long term.     

Biodiversity surrogate effectiveness in two habitat types of contrasting gradient complexity

Enormous and increasing loss of biodiversity requires evaluation of surrogate taxa as a tool for conservation biology and new reserve selection, in spite of the fact that this approach has become questionable. The aim of this study was to assess the effect of gradient complexity on species richness and community composition among three taxonomic groups. We compared efficiency of vascular plants to indicate diversity of cryptogams (bryophytes, lichens) and snails in two contrasting habitat types (treeless fens and forests) within the same geographic region. We examined correlation of their species richness (Spearman rank correlation), community composition (Bray–Curtis similarity, Mantel test) and their responses to environmental variables (detrended and canonical correspondence analysis). We also focused on Red List species. We found that spatial congruence among studied taxa was affected by habitat type, however vascular plants were good indicator of snail biodiversity in both habitats. Nevertheless, all significant positive correlations of species richness were associated with the congruence in main environmental gradients. Although there was a consistency in significantly positive cross-taxon correlation in community similarity, the congruence was insufficient for conservation purposes. Furthermore we confirmed the necessity of integration of at-risk species in conservation planning as Red List species were poor indicators for total species richness and vice versa. We suggest the complementation of existing reserve network with small-scale protected areas focused on conservation of at-risk ecosystems, communities or species. In this study vascular plants were not found as a sufficient indicator for fine-filter conservation of other taxa.     

Ants and people: a test of two mechanisms potentially responsible for the large‐scale human population–biodiversity correlation for Formicidae in Europe

Aim: Recent coarse‐scale studies have shown positive relationships between the biodiversity of plants/vertebrates and the human population. Little is known about the generality of the pattern for invertebrates. Moreover, biodiversity and human population might correlate because they both covary with other factors such as energy availability and habitat heterogeneity. Here we test these two non‐mutually exclusive mechanisms with ant species‐richness data from the Fauna Europaea. Location Forty‐three European countries/regions. Methods We derived mixed models of total, native and exotic ant species richness as a function of human population size/density, controlling for country area, plant species richness (as a proxy for habitat heterogeneity), and mean annual temperature and precipitation (variables related to energy availability). Results Ant species richness increased significantly with increasing human population. This result was confirmed when controlling for variations in country area. Both for human population size/density and for ant species richness, there were positive correlations with temperature but not with precipitation. This finding is in agreement with the energy‐availability hypothesis. However, we observed a negative latitudinal gradient in ant and plant species richness, although not in human population size/density. Plant species richness was positively correlated with ant species richness but not with human population size/density. Thus, there is evidence that this type of habitat heterogeneity can play a role in the observed latitudinal gradient of ant species richness, but not in the positive correlation between ant species richness and human population. The results were confirmed for the 545 native and the 32 exotic ant species reported, and we observed a good correlation between exotic and native ant species richness. Main conclusions Ant species richness in European countries conforms to six macroecological patterns: (1) a negative latitudinal gradient; and a positive (2) species–energy relationship, (3) species–area relationship, (4) correlation with plant species richness, (5) exotic–native species richness correlation, and (6) species–people correlation. There is some evidence for the energy‐availability hypothesis, but little evidence for habitat heterogeneity as an explanation of the large‐scale human population–ant biodiversity correlation. This correlation has implications for the conservation of ant diversity in Europe.     

Environmental effects on Neotropical liana species richness

Aim Lianas differ physiologically from trees, and therefore their species‐richness patterns and potential climate‐change responses might also differ. However, multivariate assessments of spatial patterns in liana species richness and their controls are lacking. Our aim in this paper is to identify the environmental factors that best explain the variation in liana species richness within tropical forests. Location Lowland and montane Neotropical forests. Methods We quantified the contributions of environmental variables and liana and tree‐and‐shrub abundance to the species richness of lianas, trees and shrubs ≥ 2.5 cm in diameter using a subset of 65 standardized (0.1 ha) plots from 57 Neotropical sites from a global dataset collected by the late Alwyn Gentry. We used both regression and structural equation modelling to account for the effects of environmental variables (climate, soil and disturbance) and liana density on liana species richness, and we compared the species‐richness patterns of lianas with those of trees and shrubs. Results We found that, after accounting for liana density, dry‐season length was the dominant predictor of liana species richness. In addition, liana species richness was also related to stand‐level wood density (a proxy for disturbance) in lowland forests, a pattern that has not hitherto been shown across such a large study region. Liana species richness had a weak association with soil properties, but the effect of soil may be obscured by the strong correlation between soil properties and climate. The diversity patterns of lianas and of trees and shrubs were congruent: wetter forests had a greater species richness of all woody plants. Main conclusions The primary association of both liana and tree‐and‐shrub species richness with water availability suggests that, if parts of the Neotropics become drier as a result of climate change, substantial declines in the species richness of woody plants at the stand level may be anticipated.     

Is camera trapping helping us to fill knowledge gaps related to the conservation of wild mammals?

The magnitude of human impact on biodiversity makes producing information on the conservation status of wildlife an urgent matter. Despite the increasingly widespread use of camera trapping for mammal monitoring, there are no assessments on how this tool helps fill specific knowledge gaps. We reviewed studies published between 2000 and 2018 in Mexico, a country with very high mammalian diversity, and analysed their spatial distribution. Specifically, we looked at how the number of studies at the level of the country’s states related to a) each state’s medium/large mammalian species richness and b) each state’s proportion of mammalian species classified as threatened at the national and global level. Moreover, we assessed the occurrence of studies within protected areas, terrestrial ecoregions, and mammal geographic provinces. Finally, we recorded the proportion of studies focused on estimating mammal population density and community richness that incorporated measures of variability and completeness, respectively. Based on a compilation of 191 papers published in 48 journals, we found a weak relationship between the number of studies and mammalian species richness and no clear evidence of a relationship between the number of studies and the proportion of threatened species. The studies concentrated on a few mammalian species, protected areas, forested ecoregions, and mammal geographic provinces in the country’s southern region. More than half of the studies that conducted population density estimations included measures of variability, but only one-third of the studies estimating species richness included completeness assessments. There is a need for more coordinated efforts to take full advantage of camera traps in order to produce more comprehensive and standardised surveys of the status of mammalian fauna at the country level.     

浙江定海次生林内物种丰富度与生物量和生产力关系的环境依赖性

迄今生物多样性与生态系统功能关系的研究主要在物种组成随机配置的人工生态系统中进行, 在自然生态系统中研究较少, 且未考虑环境因子如何影响生态系统功能及其与生物多样性的关系。本研究选取亚热带广泛分布的次生林为研究对象, 利用模型拟合的方法, 探讨亚热带次生林中物种丰富度与生物量和生产力之间的关系, 以及环境因子(海拔、坡度、坡向、土层厚度)和次生林恢复时间(林龄)对生物量、生产力、物种丰富度与生物量和生产力间关系的影响。结果表明, 当不考虑环境因子时, 物种丰富度与生物量之间存在显著的线性正相关关系, 而与生产力之间存在显著的二次关系(先增加后减少的驼峰型)。当考虑环境因子时, 个体密度和土层厚度对生物量具有显著影响, 而环境因子对生产力并无显著效应。在坡度较陡、坡向朝南及土层较厚的环境条件下, 物种丰富度与生物量具有显著的线性正相关关系; 而在坡度较缓、坡向朝北及土层较薄的环境条件下, 物种丰富度不影响生物量。在较高海拔环境条件下, 生产力随物种丰富度先增加后减少(驼峰形状), 而在其他环境条件下, 生产力均不响应物种丰富度。以上结果说明自然森林生态系统中物种丰富度与生物量和生产力的关系存在差异, 且其相互间的关系依赖于环境因子。     

Ecological biogeography of Malagasy non‐volant mammals: community structure is correlated with habitat

Aim To examine the relationship between ecoregions, as a proxy for regional climate and habitat type, and mammalian community structure, defined by species composition and richness (e.g. taxonomic structure) and ecological diversity (e.g. ecological structure) of non‐volant species. Location Madagascar. Methods Faunal lists of non‐volant mammal species occurring in 35 communities from five World Wildlife Fund ecoregions were collected from published and unpublished sources. Species were assigned to ecological groups defined by trophic status, locomotor habits, activity cycle and body mass. We used Mantel tests, cluster analysis and principal coordinates analysis to evaluate geographic patterning in taxonomic composition and species richness. We used stepwise multiple discriminant analysis to characterize patterns in the ecological diversity of the mammalian communities from each ecoregion. Communities from transitional habitats (e.g. representing more than one ecoregion) were used to test the predictive power of the analyses. Results Non‐volant mammal communities divided into clusters that correspond to ecoregions. There was a strong distance effect in the taxonomic structure of communities across the island and within both humid and dry forest communities, but this effect was weak within humid forest communities. Mammalian species richness was significantly lower in dry forest than in humid forest communities. The ecological structure of communities was also correlated with ecoregions. Changes in the relative percentages of omnivory, arboreal quadrupedalism, terrestrial/arboreal quadrupedalism and two body mass classes accounted for 98.1% of the variation in ecological structure. Transitional communities were projected in intermediate positions by the discriminant model. Main conclusions Our analysis demonstrates that the broad‐scale habitat and climate variables captured by the ecoregion model have shaped the assembly of non‐volant mammal communities in Madagascar over evolutionary time. The spatial pattern is consistent with ecological sorting of species ranges along environmental gradients. Historical processes, such as recent extinction and migration, may have also affected the structure of mammal communities, although these factors have played a secondary role.     

Human population, grasshopper and plant species richness in European countries

Surprisingly, several studies over large scales have reported a positive spatial correlation of people and biodiversity. This pattern has important implications for conservation and has been documented for well studied taxa such as plants, amphibians, reptiles, birds and mammals. However, it is unknown whether the pattern applies also to invertebrates other than butterflies and more work is needed to establish whether the species–people relationship is explained by both variables correlating with other environmental factors. We studied whether grasshopper species richness (Orthoptera, suborder Caelifera) is related to human population size in European countries. As expected, the number of Caelifera species increases significantly with increasing human population size. But this is not the case when controlling for country area, latitude and number of plant species. Variations in Caelifera species richness are primarily associated with variations in plant species richness. Caelifera species richness also increases with decreasing mean annual precipitation, Gross Domestic Product per capita (used as an indicator for economic development) and net fertility rate of the human population. Our analysis confirms the hypothesis that the broad-scale human population–biodiversity correlations can be explained by concurrent variations in factors other than human population size such as plant species richness, environmental productivity, or habitat heterogeneity. Nonetheless, more populated countries in Europe still have more Caelifera species than less populated countries and this poses a particular challenge for conservation.     

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.     

Variability in Energy Influences Avian Distribution Patterns Across the USA

Habitat transformations and climate change are among the most important drivers of biodiversity loss. Understanding the factors responsible for the unequal distribution of species richness is a major challenge in ecology. Using data from the North American Breeding Bird Survey to measure species richness and a change metric extracted from the MODerate resolution Imaging Spectroradiometer (MODIS), we examined the influence of energy variability on the geographic distribution of avian richness across the conterminous U.S. and in the different ecoregions, while controlling for energy availability. The analysis compared three groups of birds: all species, Neotropical migrants, and permanent residents. We found that interannual variability in available energy explained more than half of the observed variation in bird richness in some ecoregions. In particular, energy variability is an important factor in explaining the patterns of overall bird richness and of permanent residents, in addition to energy availability. Our results showed a decrease in species richness with increasing energy variability and decreasing energy availability, suggesting that more species are found in more stable and more productive environments. However, not all ecoregions followed this pattern. The exceptions might reflect other biological factors and environmental conditions. With more ecoclimatic variability predicted for the future, this study provides insight into how energy variability influences the geographical patterns of species richness. PR designed study, performed research, analyzed data and wrote paper. CAL, MAL, AMP, VCR, PDC, and EFL designed study and wrote paper.     

Environmental determinants of freshwater mollusc biodiversity and identification of priority areas for conservation in Mediterranean water courses

This study evaluates which environmental factors influence the biodiversity, distribution and conservation of freshwater mollusc communities in a Mediterranean Biosphere Reserve in the south-western Iberian Peninsula. Habitat features and two biodiversity indices (native species richness and diversity) were evaluated at 109 locations. Environmental gradients were assessed using principal component analysis, which orders the habitat variables along two gradients: headwater characteristics and water availability. According to a canonical correspondence analysis, the main environmental factors related to the distribution of species and community structure were, also, climate and headwater habitat features (precipitation, order, channel width, slope and pH), and heterogeneity and trophic features (IHF index and instream macrophytes cover). Relationships between biodiversity indices and environmental variables were best explained by a regression model incorporating, basically, aridity index and precipitation as the variables that accounted for most of the variance. This study demonstrates that distribution of freshwater molluscs along a highly stressed by drought Mediterranean region mostly depends on the local pool of species and their adaptive patterns to water availability.     

Hotspots and ecoregions: a test of conservation priorities using taxonomic data

The loss of biodiversity is now recognized as a global problem of significant magnitude [ Science 289: 2279]. Conservation efforts focus on measuring species diversity and distribution, assessing biodiversity threats, and managing habitats to maintain that diversity. The accuracy of measuring species diversity depends on the quality and scale of the data. Recently indirect estimates of diversity based on the skilled opinions of international taxonomic authorities were used to define 25 global conservation hotspots [ Nature 403: 853–858] and 871 ecoregions [ Bioscience 51: 933–938]. These data, originating from first-hand fieldwork and museum study, are readily available, but not necessarily repeatable nor testable. If this type of information prevails for conservation purposes, it is critical that we test the quality of this information with verifiable data at finer scales (e.g., regional inventories, specimen records, and accumulated distribution data). Here we perform such a test for the hotspots and ecoregions found in the Indo-Pacific by comparing the estimates of the expert scientists with authenticated published diversity data on flowering plants. We found a high correlation between our counts of species richness and endemism with the experts' estimates, but surprisingly found less congruity among the seven families examined. A revised list of conservation priority regions based on our plant data is provided.     

A comparative measure of biodiversity based on species composition

In conservation planning, species richness and species endemism are the most often used metrics for describing the biodiversity importance of areas. However, when it comes to prioritizing regions for conservation actions these measures alone are insufficient because they do not reveal how similar or different the actual composition of species may be from one area to another. For comparative analysis an additional useful metric would be one that indicates the degree to which the species assemblage in one area is also represented in—or is distinct from—species assemblages of other areas. Here we describe a method for quantifying the compositional representativeness of species assemblages among geographic regions. The method generates asymmetric pairwise similarity coefficients that are then used to calculate separate measures for the representativeness and the distinctiveness of species assemblages in the regions being compared. We demonstrate the method by comparing fish communities among freshwater ecoregions of the Mississippi Basin, and then among smaller hydrological units within two individual freshwater ecoregions. At both scales of analysis, our measures of representativeness and distinctiveness reveal patterns of fish species composition that differ from patterns of species richness. This information can enhance conservation planning processes by ensuring that priority-setting explicitly consider the most representative and distinctive species assemblages.