Elevational Species Richness Research Articles

Once upon a time: exploring the biogeographic history of the largest endemic lizard family in the Neotropics (Squamata: Gymnophthalmidae)

Abstract Gymnophthalmids are a diverse lineage of Neotropical lizards that present challenges in the understanding of their phylogenetic relationships and biogeographic history. Using a densely sampled phylogeny and distribution data, we investigated their biogeography at the family level. Dividing South and Central America into 12 regions, we tested six biogeographic models considering dispersal-extinction, vicariance, and founder events. Our analysis revealed high taxonomic and phylogenetic endemism in the Andes, Amazon, and Guiana Shield. The best-fit model identified the Guiana Shield as the likely ancestral area of the family, with dispersal events dominating over vicariance. Key areas for species interchange were the Amazon, Northern Andes, and Guiana Shield. The core regions of diversification included the Andes, Amazon, and Guiana Shield, with elevated species richness and biotic interchange events during the Eocene and Oligocene. The Guiana Shield stood out as a stronghold of gymnophthalmid diversity, driven by dispersal rates and ancient lineages. Our findings challenge previous hypotheses about the diversification of these lizards, suggesting a colonization pattern from lowlands to high elevations rather than the South-to-North Speciation Hypothesis for Andean lineages.

Rocky outcrops form islands of high and unique tree biodiversity within an ocean of grass in Serengeti National Park

AbstractAfrican savannahs are characterised by a high plant diversity, partly resulting from a high turnover in community compositions across space. However, it is poorly understood what is driving this spatial turnover in plant communities. Here, we investigate to which extent the presence of rocky outcrops (also called kopjes) explains the community composition of trees in an African savannah, and how we can understand the responses of tree species to rocky outcrops by their functional traits. Along a precipitation gradient, we visited 24 sites in Serengeti National Park (Tanzania). At each site, we characterised tree communities, as well as their functional traits, in both a kopje and an adjacent open savannah plot (matrix plot). We found that kopjes harboured elevated tree abundances and species richness. Their dominant trees were more often evergreen, had a higher specific leaf area, a lower leaf nitrogen content and a lower spine density, than dominant trees in the savannah matrix. Differences in tree communities between kopjes and savannah matrix plots were generally the largest at sites with low precipitation. Our results indicate that kopjes are strong drivers of tree biodiversity, possibly due to locally increased soil moisture and low fire frequencies. The uniqueness of kopje tree communities may have important implications for higher trophic levels and ecosystem functioning.

Fire-modulated fluctuations in nutrient availability stimulate biome-scale floristic turnover in time, and elevated species richness, in low-nutrient fynbos heathland.

In many systems, postfire vegetation recovery is characterized by temporal changes in plant species composition and richness. We attribute this to changes in resource availability with time since fire, with the magnitude of species turnover determined by the degree of resource limitation. Here, we test the hypothesis that postfire species turnover in South African fynbos heathland is powered by fire-modulated changes in nutrient availability, with the magnitude of turnover in nutrient-constrained fynbos being greater than in fertile renosterveld shrubland. We also test the hypothesis that floristic overlaps between fynbos and renosterveld are attributable to nutritional augmentation of fynbos soils immediately after fire. We use vegetation survey data from two sites on the Cape Peninsula to compare changes in species richness and composition with time since fire. Fynbos communities display a clear decline in species richness with time since fire, whereas no such decline is apparent in renosterveld. In fynbos, declining species richness is associated with declines in the richness of plant families having high foliar concentrations of nitrogen, phosphorus and potassium and possessing attributes that are nutritionally costly. In contrast, families that dominate late-succession fynbos possess adaptations for the acquisition and retention of sparse nutrients. At the family level, recently burnt fynbos is compositionally more similar to renosterveld than is mature fynbos. Our data suggest that nutritionally driven species turnover contributes significantly to fynbos community richness. We propose that the extremely low baseline fertility of fynbos soils serves to lengthen the nutritional resource axis along which species can differentiate and coexist, thereby providing the opportunity for low-nutrient extremophiles to coexist spatially with species adapted to more fertile soil. This mechanism has the potential to operate in any resource-constrained system in which episodic disturbance affects resource availability.

Ant Species Diversity in the Central and Northern Parts of the Western Sichuan Plateau in China

Understanding how species richness changes along elevational gradients has attracted increasing attention from many researchers. The relationships between species richness and elevations were characterized by monotonic decreases or mid-elevational peaks. The western Sichuan Plateau is an important species diversity hotspot. However, there is little information available about the ant species diversity and distribution patterns of this region. In this study, we hypothesize that ant diversity will show a monotonic decrease from mid-elevation with increasing elevation. Here, the ant species diversity and distribution patterns of this region were investigated by plot surveys. A total of 22,645 ants were collected from eight elevational transects in the central and northern parts of the western Sichuan Plateau, which were identified as belonging to 40 species, 18 genera, and 4 subfamilies. We found a unimodal relationship between elevation and ant species richness, with the highest ant species richness occurring at mid-elevations. The similarity coefficient of ant communities in each elevational transect was at a moderate level of dissimilarity, indicating that the elevation difference and habitat heterogeneity had a great impact on ant communities in the central and northern areas of the western Sichuan Plateau.

A comprehensive phylogeny and revised taxonomy illuminate the origin and diversification of the global radiation of Papilio (Lepidoptera: Papilionidae)

The swallowtail genus Papilio (Lepidoptera: Papilionidae) is species rich, distributed worldwide, and has broad morphological habits and ecological niches. Because of its elevated species richness, it has been historically difficult to reconstruct a densely sampled phylogeny for this clade. Here we provide a taxonomic working list for the genus, resulting in 235 Papilio species, and assemble a molecular dataset of seven gene fragments representing ca. 80% of the currently described diversity. Phylogenetic analyses reconstructed a robust tree with highly supported relationships within subgenera, although a few nodes in the early history of the Old World Papilio remain unresolved. Contrasting with previous results, we found that Papilio alexanor is sister to all Old World Papilio and that the subgenus Eleppone is no longer monotypic. The latter includes the recently described Fijian Papilio natewa with the Australian Papilio anactus and is sister to subgenus Araminta (formerly included in subgenus Menelaides) occurring in Southeast Asia. Our phylogeny also includes rarely studied (P. antimachus, P. benguetana) or endangered species (P. buddha, P. chikae). Taxonomic changes resulting from this study are elucidated. Molecular dating and biogeographic analyses indicate that Papilio originated ca. 30 million years ago (Oligocene), in a northern region centered on Beringia. A rapid early Miocene radiation in the Paleotropics is revealed within Old World Papilio, potentially explaining their low early branch support. Most subgenera originated in the early to middle Miocene followed by synchronous southward biogeographic dispersals and repeated local extirpations in northern latitudes. This study provides a comprehensive phylogenetic framework for Papilio with clarification of subgeneric systematics and species taxonomic changes enumerated, which will facilitate further studies to address questions on their ecology and evolutionary biology using this model clade.

Mechanisms behind elevational plant species richness patterns revealed by a trait‐based approach

AbstractAimsElevational patterns of plant species richness may be caused by multiple underlying mechanisms, and the same pattern can be predicted by different mechanisms. Using the steep elevational gradient of Tenerife as a model system, we aimed to test if the application of a trait‐based approach can help disentangle the role of potential mechanisms behind local elevational plant species richness patterns.LocationTenerife, Canary Islands, Spain.MethodsBased on vegetation relevés from natural vegetation and disturbed roadside habitat, along an elevational gradient of 2300 m, we observed a peak of plant species richness in the lowest third of the gradient. We considered three mechanisms potentially shaping this pattern: environmental filtering (temperature and precipitation), effects of area and disturbance. For these mechanisms, we hypothesized a distinct pattern of functional trait–elevation relationships. These were tested with in‐situ data of nine functional leaf traits, from which we calculated community‐weighted means (CWM) of traits and functional diversity (Rao's Q).ResultsWhile species richness was significantly positively correlated with temperature, area and disturbance, filtering through temperature was the only mechanism for which we could confirm most of our mechanism‐specific hypotheses about elevational trait changes: with increasing elevation, CWMs of most traits indicated shifts from acquisitive to conservative growth strategies, and functional diversity decreased. The shift of growth strategies also supported the disturbance effect, as we found overall more acquisitive communities at roadsides compared to natural habitats.ConclusionsOur results indicate that simple correlations between species richness and abiotic variables are not necessarily causal. Additional testing of mechanism‐specific hypotheses for elevational patterns of both CWMs and functional diversity can help distinguishing between correlational and mechanistic relationships between species richness and environmental variables. The trait‐based framework presented here can be fruitfully applied to better understand species richness patterns in other regions and across other types of environmental gradients.

Precipitation drives species accumulation whereas temperature drives species decline in Himalayan vertebrates

AbstractAimMany studies have explored taxon‐specific richness patterns with elevation, but few have concurrently evaluated different mechanisms to explain elevational patterns across multiple taxa. We used a novel, cross‐taxa approach to study species richness patterns combined with a framework that tests drivers of species accumulation versus decline along the elevational gradient in the Himalayas.LocationThe Himalayas.TaxonMammals, birds and amphibians.MethodsWe used geographical and elevational data of 314 mammals, 842 breeding birds and 147 amphibians to investigate species richness patterns across elevational and geographical spaces. We divided the elevational species richness gradient into segments of species accumulation versus species decline by piecewise linear regressions. We used path analysis to disentangle the direct and indirect effects of the predictors on species richness for the overall pattern and its divided segments. We test the asymmetry of main drivers between the accumulation and decline segments of richness by iteration procedure.ResultsSpecies richness for most taxa tracks an elevational hump‐shaped distribution. The dominant driver of the overall pattern varied by taxa and in context to subregion. Across taxa, precipitation best predicts the accumulation of species richness, whereas temperature best predicts the decline in species richness. Moreover, temperature and precipitation can affect species richness indirectly through productivity, showcasing a large interactional effect of climate and productivity on species richness.Main conclusionsResource allocation of the ecosystem and requirements of the species differ between the lower and upper elevation segments but remain consistent across the overall gradient. The resources essential for promoting diversity and mediating stochastic processes are directly tied to precipitation at the process of species accumulation and temperature at the process of species richness decline. Our findings support the existing theory in climate change science that reduced precipitation combined with increasing temperature may cause species extinction in the species‐rich lowlands.

Composition and distribution of polychaete assemblages associated with hydrothermal vents and cold seeps in the Bering Sea

Two areas with reducing habitats in the western Bering Sea were investigated during two expeditions onboard the RV Akademik M.A. Lavrentyev in 2016 and 2018. Hydrothermal vents of the Piip submarine volcano, located in the southwestern Bering Sea, and methane seep communities recently discovered on the Koryak slope in the northwestern Bering Sea were surveyed using a ROV Comanche 18. Species composition and distribution of polychaete (Annelida) assemblages of hydrothermal vents, cold seeps, and background sediments from the studied areas were investigated. A total of 47 species and 20 families were identified from the Piip volcano. In the area of methane emission on the Koryak slope, 86 species belonging to 32 families were collected from five separate fields at depths from 400 to 700 m. Considerable differences in structure and composition were revealed between seep polychaete assemblages, as well as between polychaete assemblages of the vent, seep, and background habitats, which showed different abundance and species richness values, sets of dominant species, and taxonomic compositions of species specific to vents and seeps. Elevated abundance and species richness values, as well as a higher diversity of the vent and seep-associated polychaete assemblages compared to the surrounding seafloor were found in vesicomyid Calyptogena pacifica beds. In contrast, the vent and seep polychaete assemblages associated with microbial mats showed a poorer family and species composition, and had a lower abundance, species richness, and diversity compared to the surrounding benthos. The variations observed in the structure and composition of polychaete assemblages are apparently associated with geochemical local conditions due to changes in intensity of toxic vent fluids and seepage emissions. The similarity between the vent and seep faunas of the studied areas of the Bering Sea was found to be low, which suggests the existence of distinct assemblages inhabiting reducing ecosystems. In addition, the higher similarity between the vent and seep polychaete assemblages was associated with vesicomyid bivalve beds. The dissimilarities between the vent and seep polychaete assemblages were mainly due to the different sets of vent- or seep-specific species.

Short-term responses of small mammal diversity to varying stand-scale patterns of retention tree patches.

Retention forestry is a common practice for biodiversity conservation in forests managed for wood production. Retention forestry often leaves unharvested patches of trees that vary in size and spatial pattern but experiments evaluating the effects of different retention patch configurations at a constant level of retention are lacking for many regions and taxonomic groups. We implemented an experimental study in clearcut conifer stands with retention across the U.S. Pacific Northwest region. The study consisted of five stand-level (11–55 ha) experimental treatments each replicated 10 times within a randomized complete block design, resulting in 50 treated stands. Retained tree density was comparable across treatments but size, number, and location (upland or riparian) of patches within stands varied among the five treatments. Within experimental treatments, we measured small mammal (<1kg) species and functional trait (i.e., body size, diet, activity stratum) richness in retention patches, surrounding harvested portions of stands, and nearby unharvested stands. We evaluated species and functional trait richness by treatment using generalized linear mixed-effects models and species-specific responses to retention placement using a community occupancy model. We obtained repeat captures of 21 species of small mammals but found limited evidence of a treatment effect on species richness, and no differences in functional trait richness. Species richness was highest where all retained trees were aggregated into one patch placed adjacent to a forested riparian buffer (mean = 6.6 species, 95% CI = 5.7–7.5), and lowest in the treatment containing one retention patch in the upland portion of a harvested stand (mean = 4.7 species, 95% CI = 3.8–5.6). Furthermore, estimates of species richness within retention patches of harvested stands (i.e., not considering species in harvested areas) did not differ among treatments, indicating that the slightly elevated species richness in riparian-associated retention results from 1–2 species in these patches that do not occur in adjacent harvested portions of each treated stand. Patch occupancy of several species was higher in riparian patches than harvested portions of the treated stands, and fewer species had higher occupancy in upland patches compared to harvested portions of treated stands. Our results indicated that at retention densities currently required in Oregon and Washington, the location of retention patches had a small influence on stand-scale measures of small mammal diversity, but local increases in species richness may be obtained by retaining trees adjacent to riparian buffers.

Species richness and turnover patterns for tropical and temperate plants on the elevation gradient of the eastern Himalayan Mountains

Understanding species’ elevational distributions in mountain ecosystems is needed under climate change, but remote biodiverse mountain areas may be poorly documented. National Forest Inventories (NFIs) offer a potential source of data. We used NFI records from Bhutan to ask three questions about elevational richness patterns of Himalayan woody plant species. First, does the mean elevation for all species differ from those species whose entire elevational distribution is recorded in the survey? Second, how does the elevation of maximum richness differ when combining species originating from temperate and tropical regions vs. analyzing them separately? And third, do the highest species turnover rates adjoin elevation zones of maximum species richness? We used 32,198 species records from 1685 forest plots along a 7570 m gradient to map species elevation ranges. Species whose entire range was documented were those whose lowest records are located above 400 m, while bare rock defined all species’ upper limits. We calculated species richness and turnover using 400 m elevation bands. Of 569 species, 79% of temperate and 61% of tropical species’ elevation ranges were fully sampled within the NFI data. Mean elevation of tree and shrub species differed significantly for temperate and tropical species. Maximum combined species richness is from 1300 to 1700 m (277 species), differing significantly from maximum tropical (900–1300 m, 169) and temperate species richness (2500–2900 m, 92). Temperate tree turnover rate was highest in the bands adjoining its maximum species richness (2500–2900 m). But turnover for tropical trees was highest several bands above their maximum species richness, where turnover and decrease in richness interact. Shrub species turnover patterns are similar, but rates were generally higher than for trees. Bhutan’s NFI records show that woody plant species are arrayed on the Himalaya in part according to floristic origins, and that combining temperate- and tropical-originating floras for gradient-based studies such as species richness and turnover obscures actual elevational patterns. In addition, species whose ranges extend below the Himalayan elevation gradient should be accounted for in future studies that correlate climate and environment factors with elevational species richness patterns.

Different temporal trends in vascular plant and bryophyte communities along elevational gradients over four decades.

Despite many studies showing biodiversity responses to warming, the generality of such responses across taxonomic groups remains unclear. Very few studies have tested for evidence of bryophyte community responses to warming, even though bryophytes are major contributors to diversity and functioning in many ecosystems. Here, we report an empirical study comparing long‐term change in bryophyte and vascular plant communities in two sites with contrasting long‐term warming trends, using “legacy” botanical records as a baseline for comparison with contemporary resurveys. We hypothesized that ecological changes would be greater in sites with a stronger warming trend and that vascular plant communities, with narrower climatic niches, would be more sensitive than bryophyte communities to climate warming. For each taxonomic group in each site, we quantified the magnitude of changes in species' distributions along the elevation gradient, species richness, and community composition. We found contrasted temporal changes in bryophyte vs. vascular plant communities, which only partially supported the warming hypothesis. In the area with a stronger warming trend, we found a significant increase in local diversity and dissimilarity (β‐diversity) for vascular plants, but not for bryophytes. Presence–absence data did not provide sufficient power to detect elevational shifts in species distributions. The patterns observed for bryophytes are in accordance with recent literature showing that local diversity can remain unchanged despite strong changes in composition. Regardless of whether one taxon is systematically more or less sensitive to environmental change than another, our results suggest that vascular plants cannot be used as a surrogate for bryophytes in terms of predicting the nature and magnitude of responses to warming. Thus, to assess overall biodiversity responses to global change, abundance data from different taxonomic groups and different community properties need to be synthesized.

Effects of Plasticity on Elevational Range Size and Species Richness.

AbstractElevational ranges within many taxa are greater in the north temperate region than the tropics. Two hypotheses to explain the pattern are, first, that large elevational ranges in the temperate region arise because species have evolved broad tolerance curves in response to seasonality and, second, that a low diversification rate in the temperate region (speciation minus extinction) has led to relatively few species, each of which occupies a large elevational range in the absence of competitors (character release). We build a quantitative genetic model of selection on a phenotypic trait, whereby increased tolerance is modeled as arising from plasticity in the trait. We show that broad tolerances result in evolution of large elevational ranges because they induce shallower genotypic clines and hence reduced maladaptive gene flow. The evolution of large elevational ranges results in relatively few competing species arranged along the elevational gradient at a species carrying capacity. In such saturated communities, species have much elevational overlap. In contrast, in similar-sized communities that could accommodate many more species, the resulting character release is associated with smaller elevational overlaps. Empirical assessment of these predictions should contribute to assessing any role for ecological limits in driving the latitudinal diversity gradient in species richness.

The Importance of Energy Theory in Shaping Elevational Species Richness Patterns in Plants.

Simple SummaryMountains are storehouses of global biodiversity; they host one-quarter of all terrestrial species at condensed spatial scales. Understanding the mechanisms and patterns that are associated with species richness along elevational gradients would help us to answer why mountains are so biologically diverse. However, despite decades of effort, a consensus regarding the processes that contribute to diversity in these locations is yet to be reached. Here, we compare the importance of four hypotheses on shaping the elevational species richness patterns of plants in 22 global mountainous regions. Moreover, a comparative analysis among different plant growth form groups was conducted to remove the influence of specific mountain attributes, such as topography complexity, history, and area. The results reveal that the performance of these hypotheses depend on the growth form and climatic conditions. The energy hypothesis provides a better explanation for the elevational species richness patterns of woody plants than the other hypotheses, while energy-related factors show greater explanatory power for predicting elevational species richness patterns in colder mountain regions. Our results highlight the importance of energy availability for the production of plant elevational species richness patterns, which is essential for the conservation and management of biodiversity.Many hypotheses have been proposed to explain elevational species richness patterns; however, evaluating their importance remains a challenge, as mountains that are nested within different biogeographic regions have different environmental attributes. Here, we conducted a comparative study for trees, shrubs, herbs, and ferns along the same elevational gradient for 22 mountains worldwide, examining the performance of hypotheses of energy, tolerance, climatic variability, and spatial area to explain the elevational species richness patterns for each plant group. Results show that for trees and shrubs, energy-related factors exhibit greater explanatory power than other factors, whereas the factors that are associated with climatic variability performed better in explaining the elevational species richness patterns of herbs and ferns. For colder mountains, energy-related factors emerged as the main drivers of woody species diversity, whereas in hotter and wetter ecosystems, temperature and precipitation were the most important predictors of species richness along elevational gradients. For herbs and ferns, the variation in species richness was less than that of woody species. These findings provide important evidence concerning the generality of the energy theory for explaining the elevational species richness pattern of plants, highlighting that the underlying mechanisms may change among different growth form groups and regions within which mountains are nested.

Range-wide habitat use of the Harpy Eagle indicates four major tropical forest gaps in the Key Biodiversity Area network

Abstract Quantifying habitat use is important for understanding how animals meet their requirements for survival and provides information for conservation planning. Currently, assessments of range-wide habitat use that delimit species distributions are incomplete for many taxa. The Harpy Eagle (Harpia harpyja) is a raptor of conservation concern, widely distributed across Neotropical lowland forests, that currently faces threats from habitat loss and fragmentation. Here, we use penalized logistic regression to identify species-habitat associations and predict habitat suitability based on a new International Union for the Conservation of Nature range metric, termed Area of Habitat. From the species-habitat model, we performed a gap analysis to identify areas of high habitat suitability in regions with limited coverage in the key biodiversity area (KBA) network. Range-wide habitat use indicated that Harpy Eagles prefer areas of 70%–75% evergreen forest cover, low elevation, and high vegetation species richness. Conversely, Harpy Eagles avoid areas of &amp;gt;10% cultivated landcover and mosaic forest, and topographically complex areas. Our species-habitat model identified a large continuous area of potential habitat across the pan-Amazonia region, and a habitat corridor from the Chocó-Darién ecoregion of Colombia running north along the Caribbean coast of Central America. Little habitat was predicted across the Atlantic Forest biome, which is now severely degraded. The current KBA network covered 18% of medium to high Harpy Eagle habitat exceeding a target biodiversity area representation of 10%, based on species range size. Four major areas of high suitability habitat lacking coverage in the KBA network were identified in north and west Colombia, western Guyana, and north-west Brazil. We recommend these multiple gaps of habitat as new KBAs for strengthening the current KBA network. Modeled area of habitat estimates as described here is a useful tool for large-scale conservation planning and can be readily applied to many taxa.

Elevational patterns in tropical bryophyte diversity differ among substrates: A case study on Baru volcano, Panama

AbstractQuestionsBryophytes attain their highest diversity in tropical mountain forests. Although distribution patterns have been described, little emphasis has been placed on comparing patterns among substrates (e.g., terrestrial, epiphytic). Understanding these patterns is important, because they determine not only the pool of genetic resources, but also the functioning of these forest ecosystems. Therefore, we studied how bryophyte species diversity changes with elevation, how elevational patterns differ between substrate types, and how elevational trends relate to environmental drivers.LocationBaru volcano, Panama.MethodsAt each of eight elevations, between 1900 and 3300 m, bryophytes were collected in 600‐cm2 plots from six substrate types with four replicates. Species cover was registered as a measure of relative abundance. Species richness and community structure were determined and related to elevation, substrate types, and environmental drivers at three scales (plots, sets of four replicate plots per substrate per elevation, and all plots at each elevation).ResultsBryophyte species richness decreased towards higher elevations, at all three scales and on all substrates except bryophytes on soil, for which, at the plot scale, richness peaked at higher elevations than on the other substrates. Relative humidity explained richness slightly better than elevation. Communities at the lowest elevations had the most uneven compositions, due to the presence of many small species with low abundance.ConclusionsIn studies on the spatial distribution of bryophyte diversity, it is essential to consider different substrates and spatial scales separately. If substrates differ in their elevational species richness patterns, climate and land‐use change may affect bryophyte diversity patterns not only directly, but also indirectly via changes in substrate availability. Therefore, a better understanding of the spatial variation in bryophyte diversity in mountains is essential to elucidate the effects of environmental change on this important group of plants and their implications for ecosystem functioning.

Assessing taxonomic and functional change in British breeding bird assemblages over time

AbstractAimThe aim was to identify the primary drivers of compositional change in breeding bird assemblages over a 40‐year period.LocationBritain.Time periodFrom 1970 to 2010.Major taxa studiedBirds.MethodsUsing morphological trait measurements and a dataset of presence–absence data for British breeding birds surveyed in 10 km × 10 km hectads during two time periods, we calculated temporal taxonomic and functional beta diversity for each hectad alongside the change in species richness, mean nearest taxon distance (MNTD) and mean pairwise distance (MPD). We also estimated potential drivers of beta diversity, including climatic and land‐use and land‐cover (LULC) change variables, elevation and assemblage species richness in 1970 (1970rich). We used random forest regressions to test which variables best explained compositional change in the assemblages. We also assessed spatial taxonomic and functional change by analysing multiple‐site beta diversity and pairwise dissimilarities between time periods.ResultsInitial (1970) species richness was the most important predictor (highest importance score) across all models, with areas characterized by higher initial richness experiencing less assemblage change overall. The coordinates included to capture spatial autocorrelation in the data were also important predictors of change. Most climate and LULC variables had relatively low explanatory power; elevation and average temperature were the most influential. All metrics increased slightly with increasing elevation, except for species richness change and MPD, which decreased.Main conclusionsThe composition of British breeding bird assemblages changed substantially between 1970 and 2010. Spatial heterogeneity increased, both taxonomically and functionally. We show evidence that hectads with larger assemblages have been buffered from temporal diversity change and that those at higher elevations changed more in composition than those at lower elevations. Overall, coarse‐resolution climate and LULC explained only small to moderate amounts of variation, suggesting that stochastic assembly change or finer‐scale drivers might be drivers of temporal changes in assemblage composition.

Environmental influence on Triatoma vitticeps occurrence and Trypanosoma cruzi infection in the Atlantic Forest of south-eastern Brazil.

Trypanosoma cruzi requires a triatomine insect vector for its life cycle, which can be complex in different enzootic scenarios, one of which is the unique transmission network in the Atlantic Forest of south-eastern Brazil. In Espírito Santo (ES) State, highly infected Triatoma vitticeps are frequently reported invading domiciles. However, triatomines were not found colonizing residences and mammals in the surrounding areas did not present T. cruzi infection. To date, the biotic and abiotic variables that modulate T. vitticeps occurrence and T. cruzi infection in ES State are still unknown. The aim of this study was to identify the environmental variables that modulate their occurrence. Local thematic maps were generated for two response variables: T. vitticeps occurrence and T. cruzi infection. The following explanatory variables were tested: climate (temperature, relative air humidity and rainfall), altitude elevation, mammalian species richness as well as soil and vegetation types. Spatiotemporal distribution patterns and correlation levels between response and explanatory variables were assessed through spatial statistics and map algebra modelling. The central and southern mesoregions presented higher T. vitticeps and T. cruzi distributions and can be considered transmission hotspots. The explanatory variables that can explain these phenomena were relative air humidity, average temperature, soil type, altitude elevation and mammalian species richness. Algebra map modelling demonstrated that central and southern mesoregions presented the environmental conditions needed for T. vitticeps occurrence and T. cruzi infection. The consideration of environmental variables is essential for understanding the T. cruzi transmission cycle. Cartographic and statistical methodologies used in parasitology have been demonstrated to be reliable and enlightening tools that should be incorporated routinely to expand the understanding of vector-borne parasite transmission.

A Small-Scale Analysis of Elevational Species Richness and Beta Diversity Patterns of Arthropods on an Oceanic Island (Terceira, Azores)

A Small-Scale Analysis of Elevational Species Richness and Beta Diversity Patterns of Arthropods on an Oceanic Island (Terceira, Azores)

A Small-Scale Analysis of Elevational Species Richness and Beta Diversity Patterns of Arthropods on an Oceanic Island (Terceira, Azores).

Simple SummaryWe studied the diversity of arthropods in native forests along a 1000 m elevation gradient on Terceira Island, Azores (Portugal). These forests form an isolated and threatened habitat with unique endemic species. We analysed the change in alpha and beta diversity of arthropod species with elevation and if the diversity of endemic, native non-endemic and introduced species responds differently to elevation. Resident arthropods were sampled using SLAM (Sea, Land and Air Malaise) traps between 2014 and 2018. Spiders (Araneae), beetles (Coleoptera), true bugs (Hemiptera) and barklice (Psocoptera), as well as endemic, native and introduced species, were analysed separately. Total species richness decreases with elevation for all species, Coleoptera and Psocoptera, and particularly so for introduced species, but peaks at mid-high elevation for Araneae and endemic species. These patterns are probably driven by unfavourable climatic conditions at higher elevations while being influenced by human disturbance at lower elevations. Total species diversity along the whole elevation gradient is shaped by this decreasing richness as well as the replacement of species at different elevations.We present an analysis of arthropod diversity patterns in native forest communities along the small elevation gradient (0–1021 m a.s.l.) of Terceira island, Azores (Portugal). We analysed (1) how the alpha diversity of Azorean arthropods responds to increasing elevation and (2) differs between endemic, native non-endemic and introduced (alien) species, and (3) the contributions of species replacement and richness difference to beta diversity. Arthropods were sampled using SLAM traps between 2014 and 2018. We analysed species richness indicators, the Hill series and beta diversity partitioning (species replacement and species richness differences). Selected orders (Araneae, Coleoptera, Hemiptera and Psocoptera) and endemic, native non-endemic and introduced species were analysed separately. Total species richness shows a monotonic decrease with elevation for all species and Coleoptera and Psocoptera, but peaks at mid-high elevation for Araneae and endemic species. Introduced species richness decreases strongly with elevation especially. These patterns are most likely driven by climatic factors but also influenced by human disturbance. Beta diversity is, for most groups, the main component of total (gamma) diversity along the gradient but shows no relation with elevation. It results from a combined effect of richness decrease with elevation and species replacement in groups with many narrow-ranged species.

Area modulates the effect of elevation but not of land use or canopy on tropical plant species richness

One of the few general patterns in ecology is the increase of species richness with area. However, factors driving species-area relationship (SAR) are under debate, and the role of human-induced changes has been overlooked so far. Furthermore, SAR studies in tropical regions, in particular in multilayered rain forests are scarce. On the other side, studies of global change-induced impacts on biodiversity have become increasingly important, particular in the tropics, where these impacts are especially pronounced. Here, we investigated if area modulates the effect of land use, elevation and canopy on plant species richness. For the first time we studied SAR in multilayered tropical forests considering all functional groups. We selected 13 natural and disturbed habitats on Kilimanjaro in Tanzania, distributed over an elevational range of 3700 m. In each habitat type, we set up three to six modified Whittaker plots. We recorded all plant species in 64 plots and 640 subplots and described SAR using the power function. Area consistently modulated effects of elevation on plant species richness, partly effects of land use but not effects of plant canopy. Thus, area needs to be taken into account when studying elevational plant species richness patterns. In contrast to temperate regions open and forest habitats did not differ in SAR, probably due to a distinct vertical vegetation zonation in tropical forests. Therefore, it is important to consider all vegetation layers including epiphytes when studying SAR in highly structured tropical regions.