Richness and composition of plants and birds on land‐bridge islands: effects of island attributes and differential responses of species groups

Aim To test relationships between the richness and composition of vascular plants and birds and attributes of habitat fragments using a model land‐bridge island system, and to investigate whether the effects of fragmentation differ depending on species natural history traits. Location Thousand Island Lake, China. Methods We compiled presence/absence data of vascular plant and bird species through exhaustive surveys of 41 islands. Plant species were assigned to two categories: shade‐intolerant and shade‐tolerant species; bird species were assigned to three categories: edge, interior, and generalist species. We analysed the relationships between island attributes (area, isolation, elevation, shape complexity, and perimeter to area ratio) and species richness using generalized linear models (GLMs). We also investigated patterns of composition in relation to island attributes using ordination (redundancy analysis). Results We found that island area explained a high degree of variation in the species richness of all species groups. The slope of the species–area relationship (z) was 0.16 for all plant species and 0.11 for all bird species. The lowest z‐value was for generalist birds (0.04). The species richness of the three plant species groups was associated with island area per se, while that of all, generalist, and interior birds was explained mainly by elevation, and that of edge bird species was associated primarily with island shape. Patterns of species composition were most strongly related to elevation, island shape complexity, and perimeter to area ratio rather than to island area per se. Species richness had no significant relationship with isolation, but species composition did. We also found differential responses among the species groups to changes in island attributes. Main conclusions Within the Thousand Island Lake system, the effects of fragmentation on both bird and plant species appear to be scale‐dependent and taxon‐specific. The number of plant species occurring on an island is strongly correlated with island area, and the richness of birds and the species composition of plants and birds are associated with variables related to habitat heterogeneity. We conclude that the effects of fragmentation on species diversity and composition depend not only on the degree of habitat loss but also on the specific patterns of habitat fragmentation.     

The relationship between nested subsets,habitat subdivision,and species diversity

Biotic assemblages are said to be nested when the species making up relatively species-poor biotas comprise subsets of the species present at richer sites. Because species number and site area are often correlated, previous studies have suggested that nestedness may be relevant to questions of how habitat subdivision affects species diversity, particularly with respect to the question of whether a single large, contiguous patch of habitat will generally contain more species than collections of smaller patches having the same total combined area. However, inferences from analyses of nestedness are complicated by (1) variability in degrees of nestedness measured in natural communities, (2) variability in species-area relationships, and (3) the fact that nestedness statistics do not account for the size of habitat patches, only in the degree of overlap among sites with different numbers of species. By comparing various indices of nestedness with a saturation index that more directly measures the effect of habitat subdivision, it is shown that the first two of these factors are not as important as the third. Whether a single large site or several smaller ones having the same total combined area maximizes species diversity is dependent on (1) overlap in species composition among sites and (2) the number of species per unit area in the different sites. Because nestedness indices do not account for species number at a site, they cannot accurately predict how habitat subdivision affects species diversity patterns. Still, nestedness analyses are important in that they indicate the degree to which rare species tend to be found in the largest, or the most species-rich, sites, patterns not revealed by the saturation index. Both types of analysis are important in order to obtain a more complete picture of how species richness and compositional patterns are influenced by habitat subdivision.     

Environmental drivers of ant species richness and composition across the Argentine Pampas grassland

Understanding the underlying mechanisms causing diversity patterns is a fundamental objective in ecology and science‐based conservation biology. Energy and environmental‐heterogeneity hypotheses have been suggested to explain spatial changes in ant diversity. However, the relative roles of each one in determining alpha and beta diversity patterns remain elusive. We investigated the main factors driving spatial changes in ant (Hymenoptera, Formicidae) species richness and composition (including turnover and nestedness components) along a 500 km longitudinal gradient in the Pampean region of Argentina. Ants were sampled using pitfall traps in 12 sample sites during the summer. We performed a model selection approach to analyse responses of ant richness and composition dissimilarity to environmental factors. Then, we computed a dissimilarity partitioning of the contributions of spatial turnover and nestedness to total composition dissimilarity. Temporal habitat heterogeneity and temperature were the primary factors explaining spatial patterns of epigean ant species richness across the Pampas. The distance decay in species composition similarity was best accounted by temperature dissimilarity, and turnover had the greatest contribution to the observed beta diversity pattern. Our findings suggest that both energy and environmental‐heterogeneity‐related variables are key factors shaping richness patterns of ants and niche‐based processes instead of neutral processes appear to be regulating species composition of ant assemblages. The major contribution of turnover to the beta diversity pattern indicated that lands for potential reconversion to grassland should represent the complete environmental gradient of the Pampean region, instead of prioritizing a single site with high species richness.     

How,and how much,natural cover loss increases species richness

Aim The species–area relationship has been applied in the conservation context to predict monotonic species richness declines as natural area is converted to human‐dominated land covers. However, some conversion of natural cover could introduce new habitat types and allow new open habitat species to occur. Moreover, decelerating richness–area relationships suggest that, as natural area is converted to human‐dominated covers, more species will be added to the rare habitat than are lost from the common one. Area effects and increased habitat diversity could each lead to a peaked relationship between species richness and the relative amount of natural area. The purpose of this study is to quantify the effect on avian species richness of conversion of natural area to human‐dominated land cover. Location Ontario, Canada. Methods We evaluated the responses of total avian richness, forest bird richness and open habitat bird richness to remaining natural area within 993 quadrats, each of 100 km². We quantified the amount of natural land cover and land‐cover heterogeneity using remote sensing data. We used structural equation modelling (SEM) to disentangle the relationships among avian richness, natural area and land‐cover heterogeneity. Results Spatial variation in avian richness was a peaked function of remaining natural area, such that losses of up to 44% of the natural area increased avian richness. This partly reflects increased variety of land cover; however, SEM suggests that much of the increase in richness is due to pure area effects. Richness of forest species declined by two species over this range of natural cover loss while open habitat bird richness increased by approximately 20 species. The effect of natural area on species richness is consistent with the sum of species–area curves for natural habitat species and human‐dominated habitat species. Main conclusions At least in northern temperate forests, almost half of the natural land cover can be converted to human‐dominated forms before avian richness declines. Conversion of < 50% of regional natural area to human‐dominated land cover can benefit open‐area species richness with relatively few losses of forest obligate species. However, with > 50% natural area conversion, species begin to drop out of regional assemblages.     

Effects of site and species characteristics on nested patterns of species composition in sedge meadows

Biotas of both geographical islands and habitat islands are often nested subsets of the biotas of successively more species-rich islands within the same system. The life history characteristics of a species may determine how that species contributes to the general pattern of species nestedness. Here, I investigate the floras of 56 sedge meadow wetlands in northern Illinois (USA) in order to characterize the degree of nestedness in these communities, determine which individual plant species contribute to the nested pattern, and investigate species characteristics that might be related to nonrandom patterns of distribution in individual plant species. The entire assemblage of species at all sedge meadows was significantly nested. Species richness and area were significantly correlated, and the nested pattern was closely related to site area, suggesting that species drop out of the assemblage in a predictable order as site area decreases. Some individual species exhibited nonrandom distributions across the sites, occurring more often in large, species-rich sites. Large sites were more likely than smaller sites to contain conservative species, i.e., those typical of pristine natural habitat, whereas nonconservative species were distributed more randomly among sites. Nested patterns of distribution of conservative species with respect to site area may result from their high probability of extinction on small sites or from a tendency for required habitats to co-occur on the same large sites. This revised version was published online in June 2006 with corrections to the Cover Date.     

Nested bird and micro-habitat assemblages in a peatland archipelago

Biotic assemblages of insular habitats are nested when poor assemblages are subsets of richer ones. Nestedness of species assemblages is frequent and may result from selective extinction or frequent colonization in insular habitats. It may also be created by a nested distribution of habitats among islands or by sampling bias. We sampled 67 isolated peatlands (7–843 ha) in southern Quebec, Canada, to measure nestedness of bird species assemblages among peatlands and assess the habitat nestedness hypothesis. Species and microhabitat assemblages were both strongly nested among peatlands. Whether sites were ranked by species richness, microhabitat richness or peatland area had no effect on nestedness. However, microhabitat nestedness was significantly reduced when sites were sorted by area rather than by microhabitat richness. As expected, if bird-microhabitat associations are responsible for the nested pattern of distribution, we found a positive correlation between the contributions of bird species and microhabitats to individual site nestedness. Nevertheless, microhabitat assemblages were significantly less nested than bird species assemblages, possibly because of frequent recolonization by birds or uneven sampling among sites. Received: 12 June 1998 / Accepted: 20 September 1998     

Vascular plant species richness on wetland remnants is determined by both area and habitat heterogeneity

There is an ongoing ecological debate on whether area per se or habitat heterogeneity is the main driver for species richness. The wetland remnants in the Sanjiang Plain, NE China harbor a high biodiversity and play an important role for local ecosystems. Fifty-one wetland remnants were sampled to examine the effect of area and habitat heterogeneity on vascular plant species richness. Number of community types, elevation, water heterogeneity and soil resource heterogeneity were employed as habitat heterogeneity variables, but only water heterogeneity was identified as the proper surrogate for habitat heterogeneity. Compared with the classic species-area model, the choros model achieved better fitness when water heterogeneity and elevation were employed as habitat heterogeneity variables. Nevertheless, elevation was poorly correlated with species richness. It suggests, without a comprehensive analysis of habitat heterogeneity variables, the choros model might result in a misleading result. In this study, species richness was significantly influenced by water heterogeneity, area and number of community types. Water heterogeneity and area both controlled the number of community types, and they were the two main determinants of species richness. As area was significantly and positively correlated with water heterogeneity, the variance in species richness was mainly related to the mutual effect of area and water heterogeneity. The results of this study confirmed that the relationship between the area per se hypothesis and the habitat heterogeneity hypothesis was conjunct rather than mutually exclusive. In addition, it is critical that both area and water heterogeneity should be taken into account for biodiversity conservation and management in wetland remnants.     

Deconstructing responses of dragonfly species richness to area,nutrients, water plant diversity and forestry

Understanding large-scale variation in species richness in relation to area, energy, habitat heterogeneity and anthropogenic disturbance has been a major task in ecology. Ultimately, variation in species richness results from variation in individual species occupancies. We studied whether the individual species occupancy patterns are determined by the same candidate factors as total species richness. We sampled 26 boreal forest ponds for dragonflies (Odonata) and studied the effects of shoreline length, water vascular plant species density (WVPSD), availability of nutrients, intensity of forestry, amount of Sphagnum peat cover and pH on dragonfly species richness and individual dragonfly species. WVPSD and pH had a strong positive effect on species richness. Removal of six dragonfly species experiencing strongest responses to WVPSD cancelled the relationship between species richness and WVPSD. By contrast, removal of nine least observed species did not affect the relationship between WVPSD and species richness. Thus, our results showed that relatively common species responding strongly to WVPSD shaped the observed species richness pattern whereas the effect of least observed, often rare, species was negligible. Also, our results support the view that, despite of the great impact of energy on species richness at large spatial scales, habitat heterogeneity can still have an effect on species richness in smaller scales, even overriding the effects of area.     

Landscape composition and habitat area affects butterfly species richness in semi-natural grasslands

During the last 50 years, the distribution and abundance of many European butterfly species associated with semi-natural grasslands have declined. This may be the result of deteriorating habitat quality, but habitat loss, resulting in decreasing area and increasing isolation of remaining habitat, is also predicted to result in reduced species richness. To investigate the effects of habitat loss on species richness, we surveyed butterflies in semi-natural grasslands of similar quality and structure, but situated in landscapes of different habitat composition. Using spatially explicit habitat data, we selected one large (6–10 ha) and one small (0.5–2 ha) grassland site (pasture) in each of 24 non-overlapping 28.2 km² landscapes belonging to three categories differing in the proportion of the area that consisted of semi-natural grasslands. After controlling for local habitat quality, species richness was higher in grassland sites situated in landscapes consisting of a high proportion of grasslands. Species richness was also higher in larger grassland sites, and this effect was more pronounced for sedentary than for mobile species. However, the number of species for a given area did not differ between large and small grasslands. There was also a significant relationship between butterfly species richness and habitat quality in the form of vegetation height and abundance of flowers. In contrast, butterfly density was not related to landscape composition or grassland size. When species respond differently to habitat area or landscape composition this leads to effects on community structure, and nestedness analysis showed that depauperate communities were subsets of richer ones. Both grassland area and landscape composition may have contributed to this pattern, implying that small habitat fragments and landscapes with low proportions of habitat are both likely to mainly contain common generalist species. Based on these results, conservation efforts should aim at preserving landscapes with high proportions of the focal habitat.     

Alien and native birds in South Africa: patterns, processes and conservation

The spatial distribution of alien species richness often correlates positively with native species richness, and reflects the role of human density and activity, and primary productivity and habitat heterogeneity, in facilitating the establishment and spread of alien species. Here, we investigate the relationship between the spatial distribution of alien bird species, human density, and anthropogenic and natural environmental conditions. Next, we examined the relationship between the spatial distribution of alien bird species and native bird species richness. We examined alien species richness as a response variable, using correlative analyses that take spatial autocorrelation into account. Further, each alien bird species was examined as a response variable, using logistic regression procedures based on binary presence–absence data. A combination of human density and natural habitat heterogeneity best explained the spatial distribution of alien species richness. This contrasts with the results for individual alien species and with previous studies on other non-native taxa showing the importance of primary productivity and anthropogenic habitat modification as explanatory variables. In general, native species richness is an important correlate of the spatial distribution of alien species richness and individual alien species, with alien species being more similar to common species than to rare species.     

Determinants of species‐area relationships for marsh‐nesting birds

ABSTRACT To clarify the underlying causes of the species‐area relationship in marsh‐nesting birds, I studied eight freshwater tidal marshes of the Connecticut River that differed in area, degree of isolation, mudflat cover, water cover, tidal regime, and extent of individual plant communities. I measured these habitat variables on aerial infrared photos, and surveyed bird populations by mapping the distribution of all birds in marshes under 5 ha in area and establishing 50‐m radius plots in marshes over 5 ha. From surveys, I determined species richness, population densities, and total populations. Analysis revealed a positive relationship between species richness and area, but no correlation between area and habitat heterogeneity. Other habitat variables were poor predictors of species richness. The lack of a relationship between habitat and species richness appeared to be a consequence of most vegetation types present not being sufficiently distinct for birds to differentially associate with them. I also found no relationship between bird population density and area, suggesting that habitat quality in marshes did not improve with increasing size, and species evenness declined with increasing richness because greater richness was associated with the presence of more rare species. Larger marshes had more rare species, species with larger populations, and species with a minimum threshold area for occurrence. Thus, my results are consistent with theoretical predictions that larger populations are less prone to local extinction and, as individuals are added to a community, more rare species are present.     

Revealing Beta-Diversity Patterns of Breeding Bird and Lizard Communities on Inundated Land-Bridge Islands by Separating the Turnover and Nestedness Components

Beta diversity describes changes in species composition among sites in a region and has particular relevance for explaining ecological patterns in fragmented habitats. However, it is difficult to reveal the mechanisms if broad sense beta-diversity indices (i.e. yielding identical values under nestedness and species replacement) are used. Partitioning beta diversity into turnover (caused by species replacement from site to site) and nestedness-resultant components (caused by nested species losses) could provide a unique way to understand the variation of species composition in fragmented habitats. Here, we collected occupancy data of breeding birds and lizards on land-bridge islands in an inundated lake in eastern China. We decomposed beta diversity of breeding bird and lizard communities into spatial turnover and nestedness-resultant components to assess their relative contributions and respective relationships to differences in island area, isolation, and habitat richness. Our results showed that spatial turnover contributed more to beta diversity than the nestedness-resultant component. The degree of isolation had no significant effect on overall beta diversity or its components, neither for breeding birds nor for lizards. In turn, in both groups the nestedness-resultant component increased with larger differences in island area and habitat richness, respectively, while turnover component decreased with them. The major difference among birds and lizards was a higher relevance of nestedness-resultant dissimilarity in lizards, suggesting that they are more prone to local extinctions derived from habitat fragmentation. The dominance of the spatial turnover component of beta diversity suggests that all islands have potential conservation value for breeding bird and lizard communities.     

Temporal variability of nestedness and idiosyncratic species in stream insect assemblages

Aims The nested subset pattern has been widely studied in the last 20 years, and recent syntheses have challenged the prevalence of this pattern in nature. We examined the degree of nestedness, its temporal variability and its environmental correlates in stream insects of a boreal drainage system. We also examined differences between nested and idiosyncratic species in site occupancy, niche position and niche breadth. Location Koutajoki drainage basin in northern Finland. Methods We used (i) nestedness analyses with three null models for testing the significance of nestedness; (ii) Spearman rank correlation to examine the correlates of nestedness; (iii) outlying mean index analysis to analyse the niche characteristics of species; (iv) and t‐test to examine differences in niche breadth, niche position and site occupancy of idiosyncratic and other nested species. Results Stream insect assemblages were significantly nested in each of the three study years. The maximally packed matrices were significantly nested according to the nestedness calculator based on null models I (species frequencies and site richness equiprobable) and II (species frequencies fixed and site richness equiprobable), but non‐significant based on a conservative null model III (species frequencies and site richness fixed to those of the observed matrix). The most important correlate of nestedness was stream size, whereas isolation, productivity (total phosphorus) and habitat heterogeneity exhibited non‐significant relationship with nestedness. Idiosyncratic species occurred, on average, at more sites than nested species, mirroring the restricted distributions of several nested species that were inclined towards species‐rich sites. Idiosyncratic and nested species also differed in niche position and niche breadth, with idiosyncratic species having, on average, less marginal niche positions and wider niches than nested species. Main conclusions Stream size correlated with nestedness, possibly because small streams were inhabited only by species able to persist under, or colonize shortly after, disturbances, while most species could occur at larger sites where disturbances are less severe. From the conservation perspective, our findings suggest that stream size really matters, given that sites with high species richness and many rare species are more likely to occur in larger streams. However, also the requirements of idiosyncratic species should be accommodated in conservation planning.     

合肥市小微湿地鸟类多样性的时空格局及其影响因素

小微湿地是城市生态系统的重要组成部分, 也是生物多样性的重要庇护场所。鸟类作为城市小微湿地生态系统的指示类群, 其多样性时空格局受多种环境因子影响。本研究于2020年8月至2021年7月采用样点法对合肥市45个小微湿地鸟类的种类、数量分布和生境因子进行了调查, 并获取湿地面积、湿地形状、建筑面积比例、植被面积比例、环境噪声、人为干扰和城市化指数等生境变量。通过α多样性和β多样性分析, 研究城市小微湿地鸟类多样性的时空特征及其决定因素。采用信息论模型选择和模型平均法以及基于距离矩阵的多重回归模型进行计算, 确定影响鸟类群落α多样性和β多样性及其组分的主要环境因子。结果显示, 研究区域共有鸟类13目39科102种, 其中水鸟31种, 国家二级重点保护鸟类2种, 安徽省重点保护鸟类17种, IUCN濒危物种红色名录中的易危(VU)物种1种。湿地面积和城市化指数对小微湿地陆地鸟类和水鸟的α多样性、β多样性及其组分均具有显著影响, 其中陆地鸟类物种丰富度在中度和低度城市化之间的小微湿地中达到最高值, 面积超过4 ha的小微湿地能维持较多的水鸟物种。植被面积比例对陆地鸟类多样性具有重要的影响, 而建筑面积比例对水鸟多样性具有显著影响。此外, 总体β多样性及其组分计算结果显示物种周转组分占明显优势, 表明城市小微湿地群作为城市复合生态系统的重要组成部分, 加强整体保护更为必要。研究结果对于加强城市鸟类保护和提高城市生态环境质量具有指导意义。     

Habitat heterogeneity overrides the species–area relationship

Aim The most obvious, although not exclusive, explanation for the increase of species richness with increasing sample area (the species–area relationship) is that species richness is ultimately linked to area-based increases in habitat heterogeneity. The aim of this paper is to examine the relative importance of area and habitat heterogeneity in determining species richness in nature reserves. Specifically, the work tests the hypothesis that species–area relationships are not positive if habitat heterogeneity does not increase with area. Location Sixteen nature reserves (area range 89–11,030 ha) in central Hungary. Methods Four-year faunistic inventories were conducted in the reserves involving c. 70 fieldworkers and 65 taxonomists. CORINE 50,000 land-cover maps were used for calculating the heterogeneity of the reserve landscape (number of habitat types, number of habitat patches and total length of edges). Results Large reserves were less heterogeneous than small reserves, probably because large reserves were established in large blocks of unproductive land whereas small reserves tended to be in more fertile land. In total, 3975 arthropod species were included in the analysis. The slope of the species–area relationship was positive only for Neuroptera and Trichoptera. There was no significant relationship in the other nine taxa examined (Collembola, Acari, Orthoptera, Thysanoptera, Coleoptera, Araneae, Diplopoda, Chilopoda, Diptera). The density (number of species ha⁻¹) of all species, however, showed a positive correlation with heterogeneity. Main conclusions The general lack of fit of species–area relationships in this study is inconsistent with most previous published studies. Importantly, and unlike many other studies, habitat heterogeneity was not correlated with reserve area in the studied system. In the absence of this source of covariation, stronger relationships were identified that suggested a fundamental link between species richness and habitat heterogeneity. The results indicate that habitat heterogeneity rather than area per se is the most important predictor of species richness in the studied system.     

Nested assemblages of Orthoptera species in the Netherlands: the importance of habitat features and life-history traits

Aim Species communities often exhibit nestedness, the species found in species‐poor sites representing subsets of richer ones. In the Netherlands, where intensification of land use has led to severe fragmentation of nature, we examined the degree of nestedness in the distribution of Orthoptera species. An assessment was made of how environmental conditions and species life‐history traits are related to this pattern, and how variation in sampling intensity across sites may influence the observed degree of nestedness. Location The analysis includes a total of 178 semi‐natural sites in the Pleistocene sand region of the Netherlands. Methods A matrix recording the presence or absence of all Orthoptera species in each site was compiled using atlas data. Additionally, separate matrices were constructed for the species of suborders Ensifera and Caelifera. The degree of nestedness was measured using the binmatnest calculator. binmatnest uses an algorithm to sort the matrices to maximal nestedness. We used Spearman’s rank correlations to evaluate whether sites were sorted by area, isolation or habitat heterogeneity, and whether species were sorted by their dispersal ability, rate of development or degree of habitat specificity. Results We found the Orthoptera assemblages to be significantly nested. The rank correlation between site order and sampling intensity was high. The degree of nestedness was lower, but remained significant when under‐ and over‐sampled sites were excluded from the analysis. Site order was strongly correlated with both size of sample site and number of habitat types per site. Rank correlations showed that species were probably ordered by variation in habitat specificity, rather than by variation in dispersal capacity or rate of development of the species. Main conclusions Variation in sampling intensity among sites had a strong impact on the observed degree of nestedness. Nestedness in habitats may underlie the observed nestedness within the Orthoptera assemblages. Habitat heterogeneity is closely related to site area, which suggests that several large sites should be preserved, rather than many small sites. Furthermore, the results corroborate a focus of nature conservation policy on sites where rare species occur, as long as the full spectrum of habitat conditions and underlying ecological processes is secured.     

Influence of area,habitat and water chemistry on richness and composition of macrophyte assemblages in southern Brazilian wetlands

Questions: Two hypotheses were tested: (1) physical features, such as wetland surface area and habitat diversity, together with water chemistry, are important determinants of species richness and composition of macrophyte assemblages and (2) species richness and composition of macrophyte assemblages differ between wetlands of different types (i.e., palustrine versus lacustrine) and between wetlands of different hydrologies (i.e. permanent versus intermittent). Location: A subtropical coastal plain segment (2500 km²) of southern Brazil. Methods: Quarterly collections were carried out in 15 wetlands (2004–2005) in southern Brazil. Differences in richness over time were tested using repeated measures ANOVA. Stepwise multiple regression was performed to investigate relationships between total richness and environmental variables. Significance of differences between wetland types and hydroperiods on species composition was verified by MRPP (Multi‐Response Permutation Procedure). The influence of the environmental variables on species composition was assessed using CCA (Canonical Correspondence Analysis). Results: Macrophyte species richness changed with time, was not significantly different between wetland types, but was higher in permanent wetlands than in intermittent ones. Area, habitat diversity and soluble reactive phosphorus concentration explained 76% of the variation in species richness. Species composition was different between permanent and intermittent wetlands, although it was not significantly different between wetland types. Area, habitat diversity and water chemistry explained 50.1% of species composition. Conclusions: Species richness and composition of wetland macrophytes were mainly determined by area, habitat diversity and hydroperiod. These results can be used for the development of conservation and management programs in southern Brazil.     

BIODIVERSITY RESEARCH: Nestedness for different reasons: the distributions of birds,lizards and small mammals on islands of an inundated lake

Aim We examined whether the community compositions of birds, lizards and small mammals were nested in a fragmented landscape in the Thousand Island Lake, China. We also assessed whether the mechanisms influencing nestedness differed among these taxonomic groups. Location Thousand Island Lake, China. Methods Presence/absence matrices were compiled for birds (42 islands) and lizards (42 islands) using line‐transect methods, and for small mammals (14 islands) using live‐trapping methods from 2006 to 2009. Nestedness was analysed using BINMATNEST, and statistical significance was assessed using the conservative null model 3. We used Spearman rank correlations and partial Spearman rank correlations to examine associations of nestedness and habitat variables (area, isolation, habitat diversity and plant richness) as well as life‐history traits (body size, habitat specificity, geographical range size and area requirement) related to species extinction and immigration tendencies. Results The community compositions of birds, lizards and small mammals were all significantly nested, but the causal factors underlying nestedness differed among taxonomic groups. For birds, island area, habitat specificity and area requirement were significantly correlated with nestedness after controlling for other independent variables. For lizards, habitat heterogeneity was the single best correlate of nestedness. For small mammals, island area, habitat heterogeneity and habitat specificity were significantly correlated with nestedness. The nested patterns of birds, lizards and small mammals were not attributable to passive sampling or selective colonization. Main conclusions The processes influencing nested patterns differed among taxonomic groups. Nestedness of bird assemblages was driven by selective extinction, and lizard assemblage was caused by habitat nestedness, while nestedness of small mammals resulted from both selective extinction and habitat nestedness. Therefore, we should take taxonomic differences into account when analysing nestedness to develop conservation guidelines and refrain from using single taxa as surrogates for others.     

Relationships between bird species and tree species assemblages in forested habitats of eastern North America

Aim We examined the relative influence of geographical location, habitat structure (physiognomy), and dominant plant species composition (floristics) on avian habitat relationships over a large spatial extent. Although it has been predicted that avian distributions are more likely to covary with physiognomy than with floristics at coarse scales, we sought to determine, more specifically, whether there remained a significant association between gradients in assemblages of bird species and dominant plant species within a general biome type, after statistically controlling for structural variation and geographical location of sampling sites. Location Our sample consisted of a subset of North American Breeding Bird Census survey sites that covered most of the range of eastern forests, from Florida to Nova Scotia, and west to Minnesota and North Dakota (up to c. 2500 km between sites). Methods We restricted our analyses to the single year (1981) that provided the largest sample of sites (47) for which vegetation data were available within ± 2 years of the avian surveys. We examined the relationship between avian community composition and tree species composition over this series of forested plots. Data were divided into four sets: (1) bird species abundances, (2) tree species abundances, (3) physiognomic or structural variables and (4) geographical location (latitude and longitude). We performed separate detrended correspondence analysis ordinations of birds and trees, before and after statistically partialling out covariation associated with structural variables and geographical location. To gauge the relationship between the two sets of species we correlated site scores resulting from separate ordinations. We also compared continental‐scale patterns of variation in bird and tree assemblages to understand possible mechanisms controlling species distribution at that scale. Results Both bird and tree communities yielded strong gradients, with first‐axis eigenvalues from 0.75 to 0.97. All gradients were relatively long (> 4.0), implying complete turnover in species composition. However, geographical location accounted for < 10% of the total variation associated with any ordination. Prior to partialling out covariation resulting from location and physiognomy, bird species ordinations were strongly correlated with tree species ordinations. The strength of association was reduced after partialling, but one bird and one tree axis remained significantly correlated. There was a significant species–area effect for birds, but not for trees. Main conclusions There was a significant relationship between bird species assemblages and tree species assemblages in the eastern forests of North America. Even after partialling out covariation associated with spatial location and forest physiognomy, there remained a significant correlation between major axes from bird and tree ordinations, consistent with the hypothesis that floristic variation is likely to be important in organizing assemblages of birds within a general biome type, albeit over a much larger spatial extent than originally predicted. Forest tree species ordinations differed from bird species ordinations in several ways: trees had a higher rate of turnover along underlying environmental gradients; trees appeared more patchily distributed than birds at this scale; and tree species were more spaced out along the underlying ecological gradients, with less overlap. By understanding the relationship between bird assemblages and forest floristics, we might better understand how avian communities are likely to change if tree species distributions are altered as a result of climatic changes.     

Woodland area,species turnover and the conservation of bird assemblages in lowland England

A study over 4 years into the number of breeding bird species and species turnover (extinctions and colonisations) in relation to area was conducted in 35 woodlands, set in an intensively farmed landscape, in north-east Essex, UK. A total of 46 species was recorded. The number of species breeding increased with woodland area; the slope of the species–area relationship did not differ between years. Habitat diversity was the only other measured variable to influence species richness. Absolute species turnover was independent of woodland area but relative turnover declined with increase in woodland area. The numbers of territories of nine species were determined. For four summer visitors the number of woods occupied increased as the overall populations increased but, for the other species, changes in overall population size led to changes in numbers in occupied woods. Chaffinch Fringilla coelebs and Song Thrush Turdus philomelos were more associated with woodland edges, Nightingale Luscinia megarhynchos, Garden Warbler Sylvia borin, Chiffchaff Phylloscopus collybita and Willow Warbler P. trochilus with interiors. Several species showed an inverse relationship between population density and woodland area. Collections of small woods hold similar species richness to single large woods. While the acquisition of large woods for conservation purposes should be a priority, the extension of smaller woods to a size of about 10 ha would be highly beneficial to both the species richness and population stability of regional woodland bird assemblages.