Bird species richness is associated with phylogenetic relatedness,plant species richness,and altitudinal range in Inner Mongolia

Bird species richness is mediated by local, regional, and historical factors, for example, competition, environmental heterogeneity, contemporary, and historical climate. Here, we related bird species richness with phylogenetic relatedness of bird assemblages, plant species richness, topography, contemporary climate, and glacial‐interglacial climate change to investigate the relative importance of these factors. This study was conducted in Inner Mongolia, an arid and semiarid region with diverse vegetation types and strong species richness gradients. The following associated variables were included as follows: phylogenetic relatedness of bird assemblages (Net Relatedness Index, NRI), plant species richness, altitudinal range, contemporary climate (mean annual temperature and precipitation, MAT and MAP), and contemporary‐Last Glacial Maximum (LGM) change in climate (change in MAT and change in MAP). Ordinary least squares linear, simultaneous autoregressive linear, and Random Forest models were used to assess the associations between these variables and bird species richness across this region. We found that bird species richness was correlated negatively with NRI and positively with plant species richness and altitudinal range, with no significant correlations with contemporary climate and glacial–interglacial climate change. The six best combinations of variables ranked by Random Forest models consistently included NRI, plant species richness, and contemporary‐LGM change in MAT. Our results suggest important roles of local ecological factors in shaping the distribution of bird species richness across this semiarid region. Our findings highlight the potential importance of these local ecological factors, for example, environmental heterogeneity, habitat filtering, and biotic interactions, in biodiversity maintenance.     

内蒙古昆虫物种多样性分布格局及其机制

物种多样性的地理分布格局及其机制是宏生态学和生物地理学的核心问题之一。区域尺度与局域尺度的影响因素, 如温度、降水、海拔变化、生境过滤、捕食、竞争与互惠等, 共同影响昆虫物种多样性的分布格局。然而, 迄今为止少有研究同时讨论不同尺度驱动因子对昆虫多样性地理分布格局的影响。本文基于内蒙古自治区86个旗县的昆虫多样性数据, 结合各地年平均气温、年降水量、古气候变化、海拔变化及植物多样性, 探讨昆虫物种多样性分布格局及其主要驱动因子。结果发现内蒙古昆虫多样性主要受到植物多样性与海拔变化的影响, 而气候因子对昆虫物种多样性的影响并不大。这一结果表明种间关系(食物多样性)与生境异质性可能对内蒙古昆虫多样性的分布格局起着主导作用。     

The influence of past and present climate on the biogeography of modern mammal diversity

Within most terrestrial groups of animals, including mammals, species richness varies along two axes of environmental variation, representing energy availability and plant productivity. This relationship has led to a search for mechanistic links between climate and diversity. Explanations have traditionally focused on single mechanisms, such as variation in environmental carrying capacity or evolutionary rates. Consensus, though, has proved difficult to achieve and there is growing appreciation that geographical patterns of species richness are a product of many interacting factors including biogeographic history and biological traits. Here, we review some current hypotheses on the causes of gradients in mammal richness and range sizes since the two quantities are intimately linked. We then present novel analyses using recent datasets to explore the structure of the environment-richness relationship for mammals. Specifically, we consider the impact of glaciation on present day mammalian diversity gradients. We conclude that not only are multiple processes important in structuring diversity gradients, but also that different processes predominate in different places.     

Changes in species diversity and canopy cover in steppe vegetation in Inner Mongolia under protection from grazing

This study describes changes in species diversity and canopy cover in relation to variation in livestock grazing in a semi-arid area in Inner Mongolia, China. Canopy cover for each species was recorded 2 and 3 years after cessation of livestock grazing, as well as in an area with continued grazing. Total species richness, alpha diversity, beta diversity and canopy cover were analysed. Sixty species were recorded during the study; 25 of them were annuals. The total number of species was the same, 52, in the grazed and the protected area, but species richness and alpha diversity per plot were lower in the area protected from grazing. The beta diversity showed little difference between the protected area and the grazed control. The total canopy cover was highest in the protected area, but the cover of annuals was higher in the grazed area. In CA ordination, the difference between treatments increased with time of protection. However, in the short period covered by this study it was difficult to separate the effects of protection from grazing and fluctuation in weather conditions, particularly of precipitation.     

Climate change and the future restructuring of Neotropical anuran biodiversity

Climate change is likely to impact multiple dimensions of biodiversity. Species range shifts are expected and may drive changes in the composition of species assemblages. In some regions, changes in climate may precipitate the loss of geographically restricted, niche specialists and facilitate their replacement by more widespread, niche generalists, leading to decreases in β-diversity and biotic homogenization. However, in other regions climate change may drive local extinctions and range contraction, leading to increases in β-diversity and biotic heterogenization. Regional topography should be a strong determinant of such changes as mountainous areas often are home to many geographically restricted species, whereas lowlands and plains are more often inhabited by widespread generalists. Climate warming, therefore, may simultaneously bring about opposite trends in β-diversity in mountainous highlands versus relatively flat lowlands. To test this hypothesis, we used species distribution modelling to map the present-day distributions of 2669 Neotropical anuran species, and then generated projections of their future distributions assuming future climate change scenarios. Using traditional metrics of β-diversity, we mapped shifts in biotic homogenization across the entire Neotropical region. We used generalized additive models to then evaluate how changes in β-diversity were associated with shifts in species richness, phylogenetic diversity and one measure of ecological generalism. Consistent with our hypothesis, we find increasing biotic homogenization in most highlands, associated with increased numbers of generalists and, to a lesser extent, losses of specialists, leading to an overall increase in alpha diversity, but lower mean phylogenetic diversity. In the lowlands, biotic heterogenization was more common, and primarily driven by local extinctions of generalists, leading to lower α-diversity, but higher mean phylogenetic diversity. Our results suggest that impacts of climate change on β-diversity are likely to vary regionally, but will generally lead to lower diversity, with increases in β-diversity offset by decreases in α-diversity.     

Ecological and evolutionary drivers of the elevational gradient of diversity

Ecological, evolutionary, spatial and neutral theories make distinct predictions and provide distinct explanations for the mechanisms that control the relationship between diversity and the environment. Here, we test predictions of the elevational diversity gradient focusing on Iberian bumblebees, grasshoppers and birds. Processes mediated by local abundance and regional diversity concur in explaining local diversity patterns along elevation. Effects expressed through variation in abundance were similar among taxa and point to the overriding role of a physical factor, temperature. This determines how energy is distributed among individuals and ultimately how the resulting pattern of abundance affects species incidence. Effects expressed through variation in regional species pools depended instead on taxon‐specific evolutionary history, and lead to diverging responses under similar environmental pressures. Local filters and regional variation also explain functional diversity gradients, in line with results from species richness that indicate an (local) ecological and (regional) historical unfolding of diversity–elevation relationships.     

环境梯度下蒙古栎群落的物种多样性特征

通过样地法研究了东北地区处于不同经度、纬度和海拔的 13个地点蒙古栎群落的物种丰富度、Gini指数、PIE指数、Shannon指数和 Pielou指数 ,利用相关和回归的统计方法分析了不同地点物种的丰富度指数、Simpson多样性指数和 Shannon多样性指数与各地所处的经度、纬度和海拔的关系。结果发现 :不仅不同地点 (较大尺度 )的物种丰富度和多样性指数均有差异 ,即使在相同的地点 (较小尺度 ) ,物种丰富度及多样性指数也有差异 ,有时还具有很大的差异 ,呈现空间异质性分布的特征 ;因为影响这些多样性指数的环境因子更加复杂 ,不仅受经度、纬度和海拔的影响 ,也受地形、群落的年龄、干扰史等多种生态因子影响。不同地点的物种丰富度与海拔和纬度都具有明显的相关性 (p<0 .0 5 ) ,物种丰富度随海拔和纬度的升高而降低 ,依据显著度的大小可以推测物种丰富度与海拔的相关性比与纬度的相关性更密切 ;蒙古栎群落不同类群的植物种的丰富度具有不同的分布格局 ,木本植物的丰富度与当地纬度具有明显的相关性 (p<0 .0 5 ) ,而与所在地的海拔没有显著的关系 (p>0 .0 5 ) ,而草本植物受海拔的影响更显著 (p<0 .0 5 ) ,而与纬度之间没有显著的关系 (p>0 .0 5 )。群落的 Gini指数、PIE指数、Shannon指数和Pielou指数未发现与海     

内蒙古罕山国家级自然保护区大型真菌多样性

本文对内蒙古罕山国家级自然保护区800余份大型真菌标本进行了研究,结合形态特征和ITS序列鉴定出308种,隶属于2门4纲14目45科108属。在科属组成上,优势科为红菇科Russulaceae、蘑菇科Agaricaceae、丝盖伞科Inocybaceae等共8科,含195种,分别占总科数、总种数的17.78%和63.31%;优势属为红菇属Russula、丝盖伞属Inocybe、蘑菇属Agaricus等共15属,分别占总属数、总种数的13.89%和54.87%。在地理分布上,以世界广布种和北温带分布种为主,分别含有128种和107种,占总种数的41.56%和34.74%,表现出明显的北温带区系特征,但不同植被类型中大型真菌多样性差异显著。     

Ecological drivers of avian diversity in a subtropical landscape: Effects of habitat diversity,primary productivity and anthropogenic disturbance

Understanding the roles of ecological drivers in shaping biodiversity is fundamental for conservation practice. In this study, we explored the effects of elevation, conservation status, primary productivity, habitat diversity and anthropogenic disturbance (represented by human population density and birding history) on taxonomic, phylogenetic and functional avian diversity in a subtropical landscape in southeastern China. We conducted bird surveys using 1‐km transects across a total of 30 sites, of which 10 sites were located within a natural reserve. Metrics of functional diversity were calculated based on six functional traits (body mass, clutch size, dispersal ratio, sociality, diet and foraging stratum). We built simultaneous autoregression models to assess the association between the ecological factors and diversity of the local avian communities. Local avian diversity generally increased with increasing habitat diversity, human population density and primary productivity. We also detected phylogenetic and functional clustering in these communities, suggesting that the avian assemblages were structured mainly by environmental filtering, rather than interspecific competition. Compared with sites outside the natural reserve, sites within the natural reserve had relatively lower avian diversity but a higher level of phylogenetic heterogeneity.     

Erosion of community diversity and stability by herbivore removal under warming

Climate change has the potential to influence the persistence of ecological communities by altering their stability properties. One of the major drivers of community stability is species diversity, which is itself expected to be altered by climate change in many systems. The extent to which climatic effects on community stability may be buffered by the influence of species interactions on diversity is, however, poorly understood because of a paucity of studies incorporating interactions between abiotic and biotic factors. Here, I report results of a 10-year field experiment, the past 7 years of which have focused on effects of ongoing warming and herbivore removal on diversity and stability within the plant community, where competitive species interactions are mediated by exploitation through herbivory. Across the entire plant community, stability increased with diversity, but both stability and diversity were reduced by herbivore removal, warming and their interaction. Within the most species-rich functional group in the community, forbs, warming reduced species diversity, and both warming and herbivore removal reduced the strength of the relationship between diversity and stability. Species interactions, such as exploitation, may thus buffer communities against destabilizing influences of climate change, and intact populations of large herbivores, in particular, may prove important in maintaining and promoting plant community diversity and stability in a changing climate.     

Global patterns of plant diversity

Summary Using 94 data sets from across the globe, we explored patterns of mean community species richness, landscape species richness, mean similarity among communities and mosaic diversity. Climate affected community species richness primarily through productivity while other climatic factors were secondary. Climatic equability affected species richness only in temperate regions where richness was greatest at high levels of temperature variability and low levels of precipitation variability. Landscape species richness correlated positively with community species richness. A global gradient in mean similarity existed but was uncorrelated with community species richness. Mean similarity was least and mosaic diversity was greatest between 25 and 30° latitude. The most diverse landscapes (low mean similarity) correlated with warm temperatures, high elevations, large areas and large seasonal temperature fluctuations. The most complex landscapes (high mosaic diversity) correlated with large areas, high productivity and warm winters. We compared diversity measures among continents and found only one significant difference: Australian landscapes have greater mosaic diversity than African landscapes. Based on our analyses we propose two hypotheses: (1) for plants, biotic interactions are more important in structuring landscapes in warmer climates and (2) longer isolated landscapes have more clearly differentiated ecological subunits.     

Global patterns of diversity among the specialist birds of riverine landscapes

1. Despite the growing view that biodiversity provides a unifying theme in river ecology, global perspectives on richness in riverine landscapes are limited. As a result, there is little theory or quantitative data on features that might have influenced global patterns in riverine richness, nor are there clear indications of which riverine landscapes are important to conservation at the global scale. As conspicuous elements of the vertebrate fauna of riverine landscapes, we mapped the global distributions of all of the world's specialist riverine birds and assessed their richness in relation to latitude, altitude, primary productivity and geomorphological complexity (surface configuration). 2. Specialist riverine birds, typical of high‐energy riverine landscapes and dependent wholly or partly on production from river ecosystems, occur in 16 families. They are represented by an estimated 60 species divided equally between the passerines and non‐passerines. Major radiation has occurred among different families on different continents, indicating that birds have evolved several times into the niches provided by riverine landscapes. 3. Continental richness varies from four species in Europe to 28 in Asia, with richness on the latter continent disproportionately larger than would be expected from a random distribution with respect to land area. Richness is greatest in mountainous regions at latitudes of 20–40°N in the riverine landscapes of the Himalayan mountains, where 13 species overlap in range. 4. Family, genus and species richness in specialist riverine birds all increase significantly with productivity and surface configuration (i.e. relief). However, family richness was the best single predictor of the numbers of species or genera. In keeping with the effect of surface configuration, river‐bird richness peaks globally at 1300–1400 m altitude, and most species occur typically on small, fast rivers where they feed predominantly on invertebrates. Increased lengths of such streams in areas of high relief and rainfall might have been responsible for species–area effects. 5. We propose the hypothesis that the diversity in channel forms and habitats in riverine landscapes, in addition to high temperature and primary productivity, have been prerequisites to the development of global patterns in the richness of specialist riverine organisms. We advocate tests of this hypothesis in other taxonomic groups. We draw attention, however, to the challenges of categorically defining riverine organisms in such tests because (i) rivers grade into many other habitat types across several different ecotones and (ii) `terrestrialisation' processes in riverine landscapes means that they offer habitat for organisms whose evolutionary origins are not exclusively riverine.     

Relative influences of current and historical factors on mammal and bird diversity patterns in deglaciated North America

Aim To investigate the relative contributions of current vs. historical factors in explaining broad‐scale diversity gradients using a combination of contemporary factors and a quantitative estimate of the temporal accessibility of areas for recolonization created by glacial retreat following the most recent Ice Age. Location The part of the Nearctic region of North America that was covered by ice sheets during the glacial maximum 20 000 BP. Methods We used range maps to estimate the species richness of mammals and terrestrial birds in 48 400 km² cells. Current conditions in each cell were quantified using seven climatic and topographical variables. Historical conditions were estimated using the number of years before present when an area became exposed as the ice sheets retreated during the post‐Pleistocene climate warming. We attempted to tease apart contemporary and historical effects using multiple regression, partial regression and spatial autocorrelation analysis. Results A measure of current energy inputs, potential evapotranspiration, explained 76–82% of the variance in species richness, but time since deglaciation explained an additional 8–13% of the variance, primarily due to effects operating at large spatial scales. Because of spatial covariation between the historical climates influencing the melting of the ice sheet and current climates, it was not possible to partition their effects fully, but of the independent effects that could be identified, current climate explained two to seven times more variance in richness patterns than age. Main Conclusions Factors acting in the present appear to have the strongest influence on the diversity gradient, but an historical signal persisting at least 13 000 years is still detectable. This has implications for modelling changes in diversity patterns in response to future global warming.     

Carbon fluxes and species diversity in grazed and fenced typical steppe grassland of Inner Mongolia,China

Aim Grasslands are dominant vegetation of China, support outstanding biodiversity and sequester bulk amount of atmospheric CO₂. These grasslands are highly degraded and fragmented due to remarkable anthropogenic and grazing loads. Chinese Government has made great attempt to restore by grazing exclusion. The relations of carbon fluxes with species composition and diversity in the communities sensitive to grazing by large herbivores are needed to be analysed under the global climate change scenario. The objective of present study was to comprehend the effects of grazing and fencing on the ecosystem structure and function of the typical steppe grassland.     

Does predator abundance influence species diversity of equilibrium macroinvertebrate assemblages in spring fens?

1. Predation may significantly control number and density of coexisting species. The effects of predation on species diversity have traditionally been tested in experiments and theoretical models of simple trophic systems. In complex natural ecosystems, however, disentangling multiple sources of variation is difficult. In groundwater-fed environments, a significant effect of predation can be expected due to the relatively stable environmental conditions; however, it has never been properly examined.
2. We analysed species diversity and total abundance of macroinvertebrate assemblages in 48 Western Carpathian spring fens, separately for whole sites and mesohabitat/season, and partitioned the effects of predation intensity from those of environmental variables in robust models using a bootstrapping technique. We verified our results by accounting for taxa resistant to predation.
3. The assumption that predation-mediated coexistence of species is the main mechanism responsible for the relatively species-rich assemblages in the Western Carpathian spring fens was not supported. However, predation may significantly influence abundance of non-predatory species and, under some conditions, it may contribute to explaining patterns in species diversity.
4. The effect of predation did not differ between the mesohabitats with different stability. However, we found higher environmental control in spring and a stronger effect of predators in autumn, which suggests that different mechanisms influence fen assemblages in different seasons.
5. Our study provides a new robust approach how to test the effect of predation on natural macroinvertebrate assemblages. The importance of predation was lower than expected in equilibrium assemblages but it may vary in time.

     

Bird diversity patterns in Neotropical temperate farmlands: The role of environmental factors and trophic groups in the spring and autumn

Productivity, habitat heterogeneity and environmental similarity are of the most widely accepted hypotheses to explain spatial patterns of species richness and species composition similarity. Environmental factors may exhibit seasonal changes affecting species distributions. We explored possible changes in spatial patterns of bird species richness and species composition similarity. Feeding habits are likely to have a major influence in bird–environment associations and, given that food availability shows seasonal changes in temperate climates, we expect those associations to differ by trophic group (insectivores or granivores). We surveyed birds and estimated environmental variables along line‐transects covering an E‐W gradient of annual precipitation in the Pampas of Argentina during the autumn and the spring. We examined responses of bird species richness to spatial changes in habitat productivity and heterogeneity using regression analyses, and explored potential differences between seasons of those responses. Furthermore, we used Mantel tests to examine the relationship between species composition similarity and both the environmental similarity between sites and the geographic distance between sites, also assessing differences between seasons in those relationships. Richness of insectivorous birds was directly related to primary productivity in both seasons, whereas richness of seed‐eaters showed a positive association with habitat heterogeneity during the spring. Species composition similarity between assemblages was correlated with both productivity similarity and geographic proximity during the autumn and the spring, except for insectivore assemblages. Diversity within main trophic groups seemed to reflect differences in their spatial patterns as a response to changes between seasons in the spatial patterns of food resources. Our findings suggest that considering different seasons and functional groups in the analyses of diversity spatial pattern could contribute to better understand the determinants of biological diversity in temperate climates.