Co-diversity and co-distribution in phyllostomid bats: Evaluating the relative roles of climate and niche conservatism

Explaining the causes of geographic gradients in biodiversity remains an elusive task. Traditionally, correlative approaches have been used to relate species richness with contemporary climate, without actually explaining the causal factors. Recent approaches propose simulation models as more appropriate tools for assessing potential causes of macroecological patterns. Here we developed stochastic models to assess the relative contribution of climate and niche conservatism in determining compositional similarity among sites (co-diversity) and geographic association among species (co-distribution) in the bat family Phyllostomidae. We used range-diversity plots and variance-ratio tests to describe and evaluate such patterns. Our results supported a strong effect of climate in determining cohesive ranges causing positive co-diversity and co-distribution. We also demonstrated a marginal effect of niche conservatism, as modeled here, among species in shaping these patterns. However, climate and niche conservatism are not sufficient and other processes are still required to explain observed patterns. Our study highlights the importance of historical processes and demonstrates the usefulness of a simulation framework in testing biogeographical hypothesis to understand the relationship between diversity and distribution.     

Untangling latitudinal richness gradients at higher taxonomic levels: familial perspectives on the diversity of New World bat communities

Aims (i) To describe at the level of local communities latitudinal gradients in the species richness of different families of New World bats and to explore the generality of such gradients. (ii) To characterize the relative effects of changes in the richness of each family to the richness of entire communities. (iii) To determine differences in the rate and direction of latitudinal gradients in species richness within families. (iv) To evaluate how differences among families regarding latitudinal gradients in species richness influence the latitudinal gradient in species richness of entire communities. Location Continental New World ranging from the northern continental United States (Iowa, 42° N) to eastern Paraguay (Canindeyú, 24° S). Methods Data on the species composition of communities came from 32 intensively sampled sites. Analyses focused on species richness of five of nine New World bat families. Multivariate analysis of variance and discriminant function analysis determined and described differences among temperate, subtropical, and tropical climatic zones regarding the species richness of bat families. Simple linear regression described latitudinal gradients in species richness of families. Path analysis was used to describe: (i) the direct effect of latitude on species richness of communities, (ii) the indirect effects of latitude on the species richness of communities through its effect on the species richness of each family, (iii) the relative effects of latitude on the species richness of bat families, and (iv) the relative contribution of each family to variation in the species richness of communities. Results Highly significant differences among climatic zones existed primarily because of a difference between the temperate zone and the tropical and subtropical zones combined. This difference was associated with the high number of vespertilionids in the temperate zone and the high number of phyllostomids in the tropical and subtropical zones. Latitudinal gradients in species richness were contingent on phylogeny. Although only three of the five families exhibited significant gradients, all families except for the Vespertilionidae exhibited indistinguishable increases in species richness with decreases in latitude. The Emballonuridae, Phyllostomidae and Vespertilionidae exhibited significant latitudinal gradients whereby the former two families exhibited the classical increase in species richness with decreasing latitude and the latter family exhibited the opposite pattern. Variation in species richness of all families contributed significantly to variation in the species richness of entire communities. Nonetheless, the Phyllostomidae made a significantly stronger contribution to changes in species richness of communities than did all other families. Much of the latitudinal gradient in species richness of communities could be accounted for by the effects of latitude on the species richness of constituent families. Main conclusions Ecological and evolutionary differences among higher taxonomic units, particularly those differences involving life‐history traits, predispose taxa to exhibit different patterns of diversity along environmental gradients. This may be particularly true along extensive gradients such as latitude. Nonetheless, species rich taxa, by virtue of their greater absolute rates of change, can dominate and therefore define the pattern of diversity at a higher taxonomic level and eclipse differences among less represented taxa in their response to environmental gradients. This is true not only with respect to how bats drive the latitudinal gradient in species richness for all mammals, but also for how the Phyllostomidae drives the latitudinal gradient for all bats in the New World. Better understanding of the mechanistic basis of latitudinal gradients of diversity may come from comparing and contrasting patterns across lower taxonomic levels of a higher taxon and by identifying key ecological and evolutionary traits that are associated with such differences.     

Species richness correlates of raw and standardized co‐occurrence metrics

Measuring β‐diversity and changes in species composition across multiple sites and environments is a major research focus in macroecology, and a variety of metrics have been proposed to quantify species co‐occurrence patterns in a species × site occurrence matrix. However, indices of β‐diversity and species co‐occurrence are often statistically dependent on the number of species in an assemblage. We compared the results of several common co‐occurrence metrics with patterns generated by a spatially explicit neutral model simulation. We found that all measures of co‐occurrence and β‐diversity, whether raw, rescaled or standardized by a null model expectation, were highly correlated with the total species richness of the landscape. The one important exception were the effect sizes of the fixed–fixed null model algorithm, which preserves row and column sums of the original matrix during matrix randomization. Our results call for a careful interpretation of meta‐analyses of assemblages that differ widely in species richness. At a minimum, observed species richness should be used as a statistical covariate in regression analyses, and results of the fixed–fixed algorithm should be compared carefully with the results of other randomization tests.     

The presence–absence matrix reloaded: the use and interpretation of range–diversity plots

Aim A great deal of information on distribution and diversity can be extracted from presence–absence matrices (PAMs), the basic analytical tool of many biogeographic studies. This paper presents numerical procedures that allow the analysis of such information by taking advantage of mathematical relationships within PAMs. In particular, we show how range–diversity (RD) plots summarize much of the information contained in the matrices by the simultaneous depiction of data on distribution and diversity. Innovation We use matrix algebra to extract and process data from PAMs. Information on the distribution of species and on species richness of sites is computed using the traditional R (by rows) and Q (by columns) procedures, as well as the new Rq (by rows, considering the structure of columns) and Qr (by columns, considering the structure by rows) methods. Matrix notation is particularly suitable for summarizing complex calculations using PAMs, and the associated algebra allows the implementation of efficient computational programs. We show how information on distribution and species richness can be depicted simultaneously in RD plots, allowing a direct examination of the relationship between those two aspects of diversity. We explore the properties of RD plots with a simple example, and use null models to show that while parameters of central tendency are not affected by randomization, the dispersion of points in RD plots does change, showing the significance of patterns of co‐occurrence of species and of similarity among sites. Main conclusion Species richness and range size are both valid measures of diversity that can be analysed simultaneously with RD plots. A full analysis of a system requires measures of central tendency and dispersion for both distribution and species richness.     

Regional variation in the historical components of global avian species richness

Aim Using a global data base of the distribution of extant bird species, we examine the evidence for spatial variation in the evolutionary origins of contemporary avian diversity. In particular, we assess the possible role of the timing of mountain uplift in promoting diversification in different regions. Location Global. Methods We mapped the distribution of avian richness at four taxonomic levels on an equal‐area 1° grid. We examined the relationships between richness at successive taxonomic levels (e.g. species richness vs. genus richness). We mapped the residuals from linear regressions of these relationships to identify areas that are exceptional in the number of lower taxa relative to the number of higher taxa. We use generalized least squares models to test the influence of elevation range and temperature on lower‐taxon richness relative to higher‐taxon richness. Results Peaks of species richness in the Neotropics were congruent with patterns of generic richness, whilst peaks in Australia and the Himalayas were congruent with patterns of both genus and family richness. Hotspots in the Afrotropics did not reflect higher‐taxon patterns. Regional differences in the relationship between richness at successive taxonomic levels revealed variation in patterns of taxon co‐occurrence. Species and genus co‐occurrence was positively associated with elevational range across much of the world. Taxon occurrence in the Neotropics was associated with a positive interaction between elevational range and temperature. Conclusions These results demonstrate that contemporary patterns of richness show different associations with higher‐taxon richness in different regions, which implies that the timing of historical effects on these contemporary patterns varies across regions. We suggest that this is due to dispersal limitation and phylogenetic constraints on physiological tolerance limits promoting diversification. We speculate that diversification rates respond to long‐term changes in the Earth's topography, and that the role of tropical mountain ranges is implicated as a correlate of contemporary diversity, and a source of diversification across avian evolutionary history.     

Species richness and structure of three Neotropical bat assemblages

We compared the assemblages of phyllostomid bats in three Neotropical rainforests with respect to species richness and assemblage structure and suggested a method to validate estimates of species richness for Neotropical bat assemblages based on mist-netting data. The fully inventoried bat assemblage at La Selva Biological Station (LS, 100 m elevation) in Costa Rica was used as a reference site to evaluate seven estimators of species richness. The Jackknife 2 method agreed best with the known bat species richness and thus was used to extrapolate species richness for an Amazonian bat assemblage (Tiputini Biodiversity Station; TBS, 200 m elevation) and an Andean premontane bat assemblage (Podocarpus National Park; BOM, 1000 m elevation) in Ecuador. Our results suggest that more than 100 bat species occur sympatrically at TBS and about 50 bat species coexist at BOM. TBS harbours one of the most species-rich bat assemblages known, including a highly diverse phyllostomid assemblage. Furthermore, we related assemblage structure to large-scale geographical patterns in floral diversity obtained from botanical literature. Assemblage structure of these three phyllostomid assemblages was influenced by differences in floral diversity at the three sites. At the Andean site, where understorey shrubs and epiphytes exhibit the highest diversity, the phyllostomid assemblage is mainly composed of understorey frugivores and nectarivorous species. By contrast, canopy frugivores are most abundant at the Amazonian site, coinciding with the high abundance of canopy fruiting trees. Assemblage patterns of other taxonomic groups also may reflect the geographical distribution patterns of floral elements in the Andean and Amazonian regions.  © 2008 The Linnean Society of London, Biological Journal of the Linnean Society , 2008, 94 , 617–629.     

Climate and plant structure determine the spatiotemporal butterfly distribution on a tropical mountain

Mountains are among the most powerful natural gradients for testing ecological and evolutionary responses of biota to environmental influences because differences in climate and plant structure occur over short spatial scales. We describe the spatiotemporal distribution patterns and drives of fruit‐feeding butterfly diversity in the mountainous region of Serra do Cipó, Minas Gerais, Brazil. Seven elevations from 822 to 1,388 m a.s.l. were selected for evaluating the effects of abiotic factors and vegetation characteristics on butterfly diversity. A total of 44 fruit‐feeding butterfly species were recorded in a two‐year study. Species richness (local and regional) of fruit‐feeding butterflies decreased with increasing elevation. The interaction between temperature or humidity and precipitation influenced the abundance and β‐diversity of butterflies in the elevation gradient, whereas β‐diversity decreased with increasing plant richness. Butterfly richness (local and regional) and β‐diversity varied with the sampling period, with fewer species in July (2012 and 2013), the dry period, as expected for Neotropical insects. β‐Diversity in space and time was due to species replacement (turnover), indicating that butterfly composition differs throughout the mountain and over time. In summary, climate and plant richness largely influence butterfly diversity in the elevational gradient. Climatic changes in conjunction with increasing anthropic impacts on mountainous regions of southeast Brazil will likely influence the community of mountaintop butterflies in the Espinhaço Mountain Range. Abstract in Portuguese is available with online material.     

Species co‐occurrence networks show reptile community reorganization under agricultural transformation

Agricultural transformation represents one of the greatest threats to biodiversity, causing degradation and loss of habitat, leading to changes in the richness and composition of communities. These changes in richness and composition may, in turn, lead to altered species co‐occurrence, but our knowledge of this remains limited. We used a novel co‐occurrence network approach to examine the impact of agricultural transformation on reptile community structure within two large (> 172 000 km²; 224 sites) agricultural regions in southeastern Australia. We contrasted assemblages from sites surrounded by intact and modified landscapes and tested four key hypotheses that agricultural transformation leads to (H1) declines in species richness, (H2) altered assemblages, (H3) declines in overall co‐occurrence, and (H4) complex restructuring of pairwise associations. We found that modified landscapes differed in composition but not richness compared with intact sites. Modified landscapes were also characterized by differences in co‐occurrence network structure; with species sharing fewer sites with each other (reduced co‐occurrence connectance), fewer highly‐connected species (truncation of the frequency distribution of co‐occurrence degree) and increased modularity of co‐occurrence networks. Critically, overall loss of co‐occurrence was underpinned by complex changes to the number and distribution of pair‐wise co‐occurrence links, with 41–44% of species also gaining associations with other species. Change in co‐occurrence was not correlated with changes in occupancy, nor by functional trait membership, allowing a novel classification of species susceptibility to agricultural transformation. Our study reveals the value of using co‐occurrence analysis to uncover impacts of agricultural transformation that may be masked in conventional studies of species richness and community composition.     

Centers of endemism and diversity patterns for typhlocybine leafhoppers （Hemiptera： Cicadellidae： Typhlocybinae） in China

This study identifies ＇centers of endemism＇ for typhlocybine leafhoppers in China, revealing diversity patterns and congruence of patterns between total species rich- ness and endemism. Distribution patterns of 774 Typhlocybinae （607 described and 167 undescribed species） were mapped on a 1.5° × 1.5° latitude/longitude grid. Total species richness, endemic species richness and weighted endemism richness were calculated for each grid cell. Grid cells within the top 5% highest values of weighted endemism richness were considered as ＇centers of endemism＇. Diversity patterns by latitude and altitude were obtained through calculating the gradient richness. A congruence of diversity patterns between total species richness and endemism was confirmed using correlation analysis. To investigate the bioclimatic factors （19 variables） contributing to the congruence be- tween total species richness and endemism, we compared the factor＇s difference between non-endemic and endemic species using the Kruskal-Wallis test. Eleven centers of en- demism, roughly delineated by mountain ranges, were identified in central and southern China, including the south Yunnan, Hengduan Mountains, Qinling Mountains, Hainan Is- land, Taiwan Island and six mountain areas located in western Sichuan, northwest Fujian, southeast Guizhou, southeast Hunan, central and western Guangdong, and north Zhejiang. Total species richness and endemic species richness decreased with increased latitude and had a consistent unimodal response to altitude. The proportions of endemism decreased with increased latitude and increased with rising altitude. Diversity patterns between total species richness and endemism were highly consistent, and ＇Precipitation of Coldest Pe- riod＇ and ＇Temperature of Coldest Period＇ may contribute to the congruence of pattern. Migration ability may play a role in the relationship of endemism and species richness; climate, environment factors and important geologic isolation events can also play crucial effect     

Using null model analysis of species co-occurrences to deconstruct biodiversity patterns and select indicator species

Aim Using total species richness to characterize biodiversity may mask multiple response patterns of species. We propose a null model analysis of species co‐occurrence‐based classification to identify sets of species that may have similar (within‐groups) and distinct (between groups) response patterns to their environment. The classification should also provide an explicit framework for selecting indicator species with characteristic co‐occurrence patterns to predict overall species richness. Location Côte‐Nord, Québec, Canada. Methods We combined null‐model of species co‐occurrence and cluster analysis to identify species groups within diverse assemblages of ground‐dwelling and flying beetles of stands in a boreal forest mosaic; we then examined their co‐occurrence and response patterns to habitat characteristics. Best subset regressions were used to select indicator species of richness within each group, from which indicators of total species richness were selected. Results The identified species groups appeared to display contrasting co‐occurrence and response patterns to at least one of the stand‐level habitat characteristics. Among flying beetles, for example, richness increased with stand‐level heterogeneity for two groups and decreased for two other groups, but the relationship was non‐significant for the total richness. We identified 28 indicator species that explained > 80% (validated by bootstrap analysis) of the variation in total species richness. Predictive performance of indicators was higher than when their co‐occurrence were reshuffled, even under a highly constrained null model, indicating that co‐occurrence patterns contributed to their predictive performance. Main conclusions Co‐occurrence‐based classification appears as a promising and effective tool for deconstructing biodiversity into species groups which reflect their ecological commonalities and differences, thus reducing the risk of making faulty inferences about the causes underlying overall diversity patterns. The method provides an explicit framework for selecting indicator species representing different species groups that may reflect the multiple responses of species co‐occurring with them. Indicator species can be effective for predicting overall species richness.     

Distorted perception of the spatial distribution of plant diversity through uneven collecting efforts: the example of Asteraceae in Australia

Aim Our aims were (1) to compare observed, estimated and predicted patterns of species richness using the Australian native Asteraceae as an example, (2) to identify candidates for hotspots of diversity for the study group, and (3) to examine the distortion of our perception of the spatial distribution of species richness through uneven or misdirected sampling efforts. Location Australia. Methods Based on data from Australia’s Virtual Herbarium, we calculated and visualized observed species richness, the Chao1 estimate of richness, the C index of collecting completeness, and an estimate of richness derived from environmental niche modelling for grid cells at a resolution of 1°. The 20 cells with the highest diversity values were used to define hotspots of diversity. Results Uneven collecting activity results in misleading diversity patterns for the family Asteraceae. While observed species richness is much higher in central Australia than in other parts of the arid interior, this is an artefact resulting from the area being a hotspot of collecting activity. The mountain ranges of south‐eastern Australia and Tasmania are candidates for unbiased hotspots of species richness. Main conclusions Vast areas of the Australian interior are insufficiently sampled on a local scale, although most of them can be expected to be relatively species poor. Some areas in the south‐east and south‐west of the continent remain undersampled relative to their high species richness. Observed species numbers, estimators and environmental niche‐modelling all have their unique advantages and disadvantages for the inference of patterns of diversity.     

Patterns of functional diversity across an extensive environmental gradient: vertebrate consumers, hidden treatments and latitudinal trends

Over the last two decades, although much has been learned regarding the multifaceted nature of biodiversity, relatively little is known regarding spatial variation in constituents other than species richness. This is particularly true along extensive environmental gradients such as latitude. Herein, we describe latitudinal gradients in the functional diversity of New World bat communities. Bat species from each of 32 communities were assigned to one of seven functional groups. Latitudinal gradients existed for the richness, diversity and scaled‐dominance of functional groups. No significant patterns were observed for evenness of functional groups. Measures of functional diversity were different in magnitude and increased towards the equator at a faster rate than expected given the underlying spatial variation in species richness. Thus, latitudinal gradient in species richness alone do not cause the latitudinal gradient in functional diversity. When variation in species composition of the regional fauna of each community was incorporated into analyses, many differences between observed and simulated patterns of functional diversity were not significant. This suggests that those processes that determine the composition of regional faunas strongly influence the latitudinal gradient in functional diversity at the local level. Nonetheless, functional diversity was lower than expected across observed sites. Community‐wide responses to variation in the quantity and quality of resources at the local level probably contribute to differences in functional diversity at local and regional scales and enhance beta diversity.     

Distribution and Local Species Diversity of Freshwater Ostracoda in Relation to Habitat in the Kahramanmaraş Province of Turkey

To understand the relationship between local (alpha) diversity of ostracods and their distribution, 95 different locations were randomly sampled from southern Kahramanmaraş (Turkey) between 7 June and 31 July, 2010. Total of 46 ostracods were encountered from 68 sites. Four alpha diversity indices (Shannon‐Wiener, Menhinick, Brillouin, Margalef) individually quantified higher species diversity and evenness for three types of habitats (limnocrene springs, ponds, stream). Diversity partitioning analyses revealed a significant and substantial beta‐diversity among the sites. First axis of CCA exhibited about 71% of the correlations between species and environmental variables. Water temperature, having either a negative or positive correlation with individual species, was the most influential factor affecting diversity. Altitude did not significantly affect the numbers of species identified from the elevation ranges of 400–600 m and 800–1000 m. At least nine cosmopolitan species from 56 sites had an important contribution to local diversity. Hence, suitability of aquatic (ecological) conditions and habitat types provide better explanations for ostracod diversity than do other abiotic factors such as altitude, pH and salinity. The results may support the Habitat Diversity Hypothesis but the study needs to be expanded to different regions and cannot be generalized at the moment. (© 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Moth diversity,species composition,and distributional pattern in Aravalli Hill Range of Rajasthan,India

Moths are phytophagous, cosmopolitan, agricultural pests, night pollinators, chiefly nocturnal and potential bio-indicators. The current study will be the first report on species diversity, species composition, abundance, and distributional pattern of moth fauna in Aravalli Hill Range Rajasthan. During the survey period of 2018–2019, 758 specimens of moths were collected pertaining to 34 species, 26 genera belonging to 05 families, and 13 subfamilies from three different sites of Aravalli Hill Range. Based on the number of genera, family Sphingidae was most dominant with 9 genera, and family Crambidae was least dominant with 2 genera. Based on the number of species, the family Sphingidae was the most dominant, representing 13 species, followed by Erebidae representing 11 species, Saturniidae and Noctuidae with 4 species each, the least dominant was Crambidae with 2 species. The diversity indices for moths have been calculated for the first time from the Aravalli Range of Rajasthan. Across the survey, Simpson’s Diversity Index (D′), Shannon Diversity Index (H′), Dominance & Evenness was calculated as 0.95, 3.3, 0.04, and 0.8, respectively, which reflects that moth fauna is diverse in the surveyed areas.     

The diversity of insectivorous bat assemblages among habitats within a subtropical urban landscape

We investigated the bat (Microchiroptera) diversity of four major habitat types within a large Australian subtropical city (Brisbane, Australia) to determine whether species richness was affected by habitat changes associated with urbanization, as suggested from studies elsewhere. Forty sites, ten in each habitat type (remnant bushland, parkland, low‐density residential and high‐density residential) were surveyed using acoustic bat detectors on six non‐consecutive occasions. Fourteen bat species were recorded. The species accumulation curve of the entire Brisbane bat assemblage reached a plateau at 14 species. The total numbers of species in bushland, parkland, low‐density residential and high‐density residential habitats were 14, 13, 14 and 11 species, respectively. Asymptotic estimates of species richness for each habitat were close or equal to these totals. Mean asymptotic estimated species richness differed significantly among habitats, being lowest in high‐density residential sites and highest in low‐density residential sites. Evenness profiles were similar across habitats, and were not strongly dominated by a few species. Partitioning of diversity components showed that landscape (γ) diversity was mainly determined by the high species richness of low‐density residential and bushland habitats (α diversity), rather than high beta (β) diversity among habitats. These findings contradict those of other studies on bat diversity in which species richness was highest within ‘natural’ areas of the urban landscape and assemblages were dominated by one or two species. This highlights the need for caution in making generalizations based on existing information, which is dominated by studies in temperate regions.     

Richness and diversity of Leguminosae in an altitudinal gradient in the tropical semi‐arid zone of Brazil

Abstract Many studies are based on the premise that, on a local scale, diversity is the result of ecological processes, whereas on a regional scale factors such as the topography, geology, hydrology, and historical and evolutionary events would influence this control. The Baturité Mountain Range (Ceará state), located in the Brazilian semi‐arid zone, is considered an area of extreme importance for conservation with its vegetation varying with the altitude and slope (windward vs. leeward). On the windward (wet) slope, rainforest dominates, whereas the leeward (dry) slope is dominated by seasonal forests and thorny woodland. The aim of this study was to contribute to the knowledge of the patterns of richness and diversity of the family Leguminosae on a local scale (Baturité Mountain Range) as well as a regional scale (northeastern Brazil). The two slopes present quite distinct floras. The dry slope presents higher richness and diversity indices for Leguminosae than the wet slope. The highest diversity of Leguminosae in the dry areas did not corroborate the ideas of other studies carried out in neotropical forests (total flora) that the higher species richness was predicted for wet areas. The present study indicates that the historical and evolutionary processes influence the diversity patterns on a local scale (Baturité Mountain Range), as well as on a regional scale (Brazilian semi‐arid). Our results reinforce the uniqueness of each portion of this area and its importance for conservation.     

Butterfly diversity at the ecotone between agricultural and semi‐natural habitats across a climatic gradient

Aim Understanding the response of species to ecotones and habitat edges is essential to designing conservation management, especially in mosaic agricultural landscapes. This study examines how species diversity and composition change with distance from semi‐natural habitats, over ecotones into agricultural fields, and how within‐site patterns of community transition change across a climatic gradient and differ between crop types. Location A total of 19 sites in Israel where semi‐natural habitats border agricultural fields (wheat fields or olive groves) distributed along a sharp climatic gradient ranging between 100 and 800 mm mean annual rainfall. Methods  We performed butterfly surveys in 2006. We analysed species richness (α‐diversity), diversity, community nestedness and species turnover (β‐diversity) within sites and between sites (γ‐diversity). We also assessed where species of conservation concern occurred. Results In wheat sites, richness and diversity declined abruptly from ecotones to fields and remained homogenously poor throughout the fields, regardless of climate. In olive sites, despite the sharp structural boundary, richness and diversity remained high from the semi‐natural habitat to the grove margins and then declined gradually into groves. Species of conservation concern occurred across all habitats at olive sites, but none were found inside wheat fields or at their ecotones. The contrast in community structure between semi‐natural habitats and fields was affected by both climate and field type. Irrigation in arid regions did not augment species diversity. Main conclusions Our results indicate that consideration of crop type, within a climatic context, should receive high priority in biodiversity conservation in agricultural areas. In ‘hostile’ crops, such as wheat, we suggest favouring a combination of high‐intensity management and wide margins over less intensive management without margins, which may merely aid generalist butterfly species. The scarcity of butterflies in arid irrigated fields suggests a need to carefully assess the effects of irrigation and agrochemicals on species’ communities.     

Bat diversity of a Cerrado habitat in central Brazil

The Cerrado is considered one of the 25 biodiversity hotspots in the world by conservation organizations. There are few studies on bat taxonomic groups for this biome. Herein we present a bat survey employing mist nets in the protected area of a private natural heritage reserve Reserva Particular do Patrimônio Natural Pousada das Araras, located in the west-central Brazil. We investigate the hypothesis that the Cerrado habitat complexity plays a role on the different structuring forces in bat ecological communities. Bats represent a diversity of trophic levels, and they occupy a wide range of available Cerrado habitats and microhabitats. The patterns and processes we discuss represent the factors influencing coexisting species of bats in different habitats and their implications for conservation. We captured 758 individuals of 25 species belonging to four families. Phyllostomidae was the dominant family, represented by 20 species (80%). The average recapture rate was 6.2%, and the species with most proportional recapture was A. caudifer. Greater species richness was observed among bats with predominantly insectivore habits, followed by frugivores. Glossophaga soricina was a dominant species, with about 30% of the captures. There was seasonal variation relating to the number of bats captured, with greater bat frequency occurring during the wet season, although some species occurred at higher rates during the dry season, such as C. perspicillata and S. lilium. Sanguivore bats were abundant, reflecting the availability of shelters and food supply (livestock) in the surrounding area. Compared to other surveyed areas, Pousada das Araras may be considered of high species diversity, supplanting the majority of known Cerrado studied areas. Apparently Cerrado favours the occurrence of insectivore species, with emphasis on the foliage-gleaning insectivores belong to the subfamily Phyllostominae. This study indicates that apparently the conservation of the Cerrado savanna fragments can support a considerable diversity of bat species.     

Contrasting patterns in local and zonal family richness of stream invertebrates along an Andean altitudinal gradient

1. Describing and understanding patterns in biological diversity along major geographical gradients is an important topic in ecology. Samples collected from a large number of physically and chemically comparable stream sites along a 4000 m gradient of altitude in the Andes of Ecuador served to characterise patterns of family richness of aquatic macroinvertebrates at the scale of the stream site (local) and at that of discrete altitudinal zones. 2. Both mean local and zonal family richness decreased by about 50% from sea level to 4000 m a.s.l. Local richness declined linearly, while zonal richness remained constant from sea level up to a threshold altitude of about 1800 m, whereafter it decreased. 3. From sea level to 1800 m few families were lost from zonal richness and few were gained. From 1800 to 3800 m the decrease in the number of families was accounted for by a loss of families present in lowland streams, with few new families gained. Hence, there was relatively little turnover of families along the entire gradient. 4. The diverging pattern of local and zonal richness was caused by sporadically occurring families inflating zonal richness at mid‐altitudes. If the sporadic families were represented by the same species found commonly in the lowlands, then the mid‐altitudinal zonal richness would be maintained by a ‘rescue effect’. More probably, however, the sporadically occurring families found at mid‐altitudes are each represented by new species replacing each other along the gradient, the families progressively diminishing in species richness and occurrence as the overall temperature tolerance of the family is approached. 5. This study demonstrates that spatial scale affects altitudinal patterns in the taxonomic richness of stream invertebrates. It also showed that family‐level identification can facilitate interpretation of sources and sinks of biodiversity along geographic gradients.     

Diversity and species composition of West African ungulate assemblages: effects of fire,climate and soil

Aim Anthropogenic fires are a major component of the ecology of rangelands throughout the world. To assess the effects of these fires on the diversity patterns of herbivores, we related gradients in fire occurrence, climate and soil fertility to patterns in alpha and beta diversity of African ungulates. Location West Africa. Methods We used a survey‐based approach for ungulates in 37 protected areas in desert, savanna and rain forest habitats throughout West Africa, combined with satellite images of fire occurrence and digital maps of actual evapotranspiration and soil fertility. Alpha diversity was related to the environmental variables using conventional and spatial regression models. We investigated beta diversity using partial Mantel tests and ordination techniques, and by partitioning the variance in assemblage composition into environmental and spatial components. Results The species richness of grazers showed a quadratic relationship with actual evapotranspiration, whereas that of browsers and frugivores showed a linear relationship. However, in the multiple regression models fire occurrence was the only variable that significantly correlated with the species richness of grazers. Soil fertility was weakly related to overall beta diversity and the species richness of browsers, but was non‐significant in the multiple regression models. Fire occurrence was the most important variable explaining species composition of the overall species set and of grazers, whereas the assemblage composition of browsers and frugivores was explained mostly by actual evapotranspiration. Main conclusions In contrast to previous studies, our analyses show that moisture and nutrients alone fail to adequately predict the diversity patterns of grazing ungulates. Rather, the species richness and assemblage composition of grazers are largely governed by anthropogenic fires that modify the quality and structure of the grass sward. Diversity patterns of browsers and frugivores are markedly different from grazers and depend mainly on the availability of moisture, which is positively correlated with the availability of foliage and fruits. Our study highlights the importance of incorporating major human‐induced disturbances or habitat alterations into analyses of diversity patterns.