Spatial diversity patterns of Pristimantis frogs in the Tropical Andes

Although biodiversity gradients have been widely documented, the factors governing broad‐scale patterns in species richness are still a source of intense debate and interest in ecology, evolution, and conservation biology. Here, we tested whether spatial hypotheses (species–area effect, topographic heterogeneity, mid‐domain null model, and latitudinal effect) explain the pattern of diversity observed along the altitudinal gradient of Andean rain frogs of the genus Pristimantis. We compiled a gamma‐diversity database of 378 species of Pristimantis from the tropical Andes, specifically from Colombia to Bolivia, using records collected above 500 m.a.s.l. Analyses were performed at three spatial levels: Tropical Andes as a whole, split in its two main domains (Northern and Central Andes), and split in its 11 main mountain ranges. Species richness, area, and topographic heterogeneity were calculated for each 500‐m‐width elevational band. Spatial hypotheses were tested using linear regression models. We examined the fit of the observed diversity to the mid‐domain hypothesis using randomizations. The species richness of Pristimantis showed a hump‐shaped pattern across most of the altitudinal gradients of the Tropical Andes. There was high variability in the relationship between area and species richness along the Tropical Andes. Correcting for area effects had little impact in the shape of the empirical pattern of biodiversity curves. Mid‐domain models produced similar gradients in species richness relative to empirical gradients, but the fit varied among mountain ranges. The effect of topographic heterogeneity on species richness varied among mountain ranges. There was a significant negative relationship between latitude and species richness. Our findings suggest that spatial processes partially explain the richness patterns of Pristimantis frogs along the Tropical Andes. Explaining the current patterns of biodiversity in this hot spot may require further studies on other possible underlying mechanisms (e.g., historical, biotic, or climatic hypotheses) to elucidate the factors that limit the ranges of species along this elevational gradient.     

Bird diversity along elevational gradients in the Andes of Colombia: area and mass effects

Aim The decrease in species richness with increasing elevation is a widely recognized pattern. However, recent work has shown that there is variation in the shape of the curve, such that both negative monotonic or unimodal patterns occur, influenced by a variety of factors at local and regional scales. Discerning the shape of the curve may provide clues to the underlying causes of the observed pattern. At regional scales, the area of the altitudinal belts and mass effects are important determinants of species richness. This paper explores the relationship between bird species richness, elevation, mass effects and area of altitudinal zones for birds in tropical mountains. Location The three Andean ranges of Colombia and the peripheral mountain ranges of La Macarena and Santa Marta. Methods Lists of bird species were compiled for altitudinal belts in eastern and western slopes of the three Andean Cordilleras and for La Macarena and Santa Marta. The area of the altitudinal belts was computed from digital elevation models. The effect of area was analysed by testing for differences among altitudinal belts in the slopes and intercepts of the species‐area relationships. Mass effects were explored by separately analysing two sets of species: broadly distributed species, i.e. lowland species whose distributions extend into the Andes, and tropical Andean species, i.e., species that evolved in the Andes. Results Plotting total number of species in each altitudinal belt revealed a decline in species richness with elevation. In slopes with a complete elevational gradient from lowlands to mountain peaks, the decrease was monotonic. In internal Andean slopes where the lower elevational belts are truncated, there was a peak at mid elevations. There was a linear relationship between number of species and area of the altitudinal belts. When controlling for area, there were no differences in the number of species among altitudinal belts (500–2600 m), except for the two upper‐elevation zones (2600–3200 and > 3200 m), which had lower species richness. Diversity of widely distributed species declined monotonically with elevation, whereas tropical Andean species exhibited a mid‐elevation peak. Main conclusions A large proportion of the variation in species richness with elevation was explained by area of the altitudinal belts. When controlling for area, species richness remained constant up to 2600 m and then decreased. This pattern contrasts with a previously reported hump‐shaped pattern for Andean birds. Diversity patterns of widely distributed species suggested that immigration of lowland species inflates diversity of lower elevational belts through mass effects. This influence was particularly evident in slopes with complete altitudinal gradients (i.e. connected to the lowlands). Tropical Andean species, in contrast, were more diverse in mid‐elevational belts, where speciation rates are expected to be higher. The influence of these species was more prevalent in internal Andean slopes with no connection to the lowlands. The decline of species richness at high elevations may be related to higher extinction rates and lower resource levels.     

Elevational gradients in ant species richness: area, geometry, and Rapoport's rule

Studying the distributions of plants and animals along environmental gradients can illuminate the factors governing and maintaining species diversity. There are two general predictions of how species richness and elevation are related: either species richness decreases monotonically with increasing elevation or richness peaks at mid-elevations. Several processes might contribute to this pattern. In this paper, I examine patterns in ant species richness along elevational gradients in three states in the western US: Colorado, Nevada, and Utah. I test for the effects of available area and the geometric constraints model on species richness patterns. I also test Rapoport's rescue hypothesis, which relates the extent of species' elevational ranges to patterns in species richness. In each state, species richness peaked at mid-elevations. Area explained more variation in species richness than the geometric constraints model in Colorado and Utah, but not in Nevada. Area and geometric constraints together explained 90%, 99%, and 57% of the variation in species richness in Colorado, Nevada, and Utah, respectively. Even though there were peaks at mid-elevations, I still found a strong Rapoport effect. This work suggests that the influences of area and geometric constraints cannot be overlooked when examining patterns in species richness along environmental gradients.     

Elevational Gradient of Vascular Plant Species Richness and Endemism in Crete – The Effect of Post-Isolation Mountain Uplift on a Continental Island System

Understanding diversity patterns along environmental gradients and their underlying mechanisms is a major topic in current biodiversity research. In this study, we investigate for the first time elevational patterns of vascular plant species richness and endemism on a long-isolated continental island (Crete) that has experienced extensive post-isolation mountain uplift. We used all available data on distribution and elevational ranges of the Cretan plants to interpolate their presence between minimum and maximum elevations in 100-m elevational intervals, along the entire elevational gradient of Crete (0–2400 m). We evaluate the influence of elevation, area, mid-domain effect, elevational Rapoport effect and the post-isolation mountain uplift on plant species richness and endemism elevational patterns. Furthermore, we test the influence of the island condition and the post-isolation mountain uplift to the elevational range sizes of the Cretan plants, using the Peloponnese as a continental control area. Total species richness monotonically decreases with increasing elevation, while endemic species richness has a unimodal response to elevation showing a peak at mid-elevation intervals. Area alone explains a significant amount of variation in species richness along the elevational gradient. Mid-domain effect is not the underlying mechanism of the elevational gradient of plant species richness in Crete, and Rapoport''s rule only partly explains the observed patterns. Our results are largely congruent with the post-isolation uplift of the Cretan mountains and their colonization mainly by the available lowland vascular plant species, as high-elevation specialists are almost lacking from the Cretan flora. The increase in the proportion of Cretan endemics with increasing elevation can only be regarded as a result of diversification processes towards Cretan mountains (especially mid-elevation areas), supported by elevation-driven ecological isolation. Cretan plants have experienced elevational range expansion compared to the continental control area, as a result of ecological release triggered by increased species impoverishment with increasing elevation.     

Altitudinal patterns of plant species richness on the Baekdudaegan Mountains, South Korea: mid-domain effect, area, climate, and Rapoport’s rule

We studied the altitudinal patterns of plant species richness and examined the effects of geometric constraints, area, and climatic factors on the observed richness patterns along the ridge of the Baekdudaegan Mountains, South Korea. Rapoport’s altitudinal rule was evaluated by examining the relationship between altitudinal range size and midpoint. We also examined the latitudinal effect on species richness. Plant data were collected from 1,100 plots along a 200–1,900 m altitudinal gradient along the ridge of the Baekdudaegan. A total of 802 plant species from 97 families and 342 genera were found. The altitudinal patterns of plant species richness along the ridge of the Baekdudaegan depicted distinctly hump-shaped patterns, although the absolute altitudes of the richness peaks vary somewhat among plant groups. While the mid-domain effect (MDE) was the most powerful explanatory variable in simple regression models, species richness was also associated with climatic factors, especially mean annual precipitation (MAP) and temperature (MAT) in multiple regression models. The relative importance of the MDE and climatic factors were different among plant groups. The MDE was more important for woody plants and for large-ranged species, whereas climatic factors were better predictors for total and herbaceous plants and for small-ranged species. Rapoport’s altitudinal rule and a latitudinal effect on species richness were not supported. Our study suggests that a combined interaction of the MDE and climatic factors influences species richness patterns along the altitudinal gradient of the Baekdudaegan Mountains, South Korea.     

Species Richness of Nonvolant Small Mammals Along Elevational Gradients in Northwestern Argentina

The Nevados del Aconquija (5500 m) and Cumbres Calchaquíes (4600 m) are isolated mountain ranges that contain at least three physiognomic units in their eastern slopes: Neotropical rainforests, Andean grasslands and High Andean Steppes. Despite phytogeographical similarities, the two ranges differ in the amount and spatial distribution of rainfall over the elevation gradient. We studied terrestrial small mammals by direct trapping in two altitudinal transects on the eastern slope of the two mountain ranges. We recorded the changes in richness and species composition, as well as the relationships between species and microhabitats at each altitudinal level. The results show a similar structure of the small mammal assemblage in the two ranges. The largest differences, in terms of species composition, were registered at lower elevation forests, and faunal affinities increased with elevation to the point of finding identical species composition at the top of the mountains. Species richness showed a clear curvilinear pattern with a peak at the upper limit of the forests. Our findings suggest that total rainfall has an important influence on the composition and abundance of small mammal species but apparently not on the species richness along the elevation gradient. The highest values of species richness were observed at the sites where a contact between two different physiognomic units exists. These results indicate that habitat heterogeneity plays an important role in allowing the juxtaposition of small terrestrial mammal assemblages of the highlands and lowlands at a given point, contributing significantly to the considerable diversity of species observed in intermediate altitudinal sites.
     

Small mammal species richness and turnover along elevational gradient in Yulong Mountain,Yunnan, Southwest China

Understanding the species diversity patterns along elevational gradients is critical for biodiversity conservation in mountainous regions. We examined the elevational patterns of species richness and turnover, and evaluated the effects of spatial and environmental factors on nonvolant small mammals (hereafter “small mammal”) predicted a priori by alternative hypotheses (mid‐domain effect [MDE], species–area relationship [SAR], energy, environmental stability, and habitat complexity]) proposed to explain the variation of diversity. We designed a standardized sampling scheme to trap small mammals at ten elevational bands across the entire elevational gradient on Yulong Mountain, southwest China. A total of 1,808 small mammals representing 23 species were trapped. We observed the hump‐shaped distribution pattern of the overall species richness along elevational gradient. Insectivores, rodents, large‐ranged species, and endemic species richness showed the general hump‐shaped pattern but peaked at different elevations, whereas the small‐ranged species and endemic species favored the decreasing richness pattern. The MDE and the energy hypothesis were supported, whereas little support was found for the SAR, the environmental stability hypothesis, and the habitat complexity. However, the primary driver(s) for richness patterns differed among the partitioning groups, with NDVI (the normalized difference vegetation index) and MDE being the most important variables for the total richness pattern. Species turnover for all small mammal groups increased with elevation, and it supported a decrease in community similarity with elevational distance. Our results emphasized for increased conservation efforts in the higher elevation regions of the Yulong Mountain.     

A comparison of altitudinal species richness patterns of bryophytes with other plant groups in Nepal, Central Himalaya

Aim To explore species richness patterns in liverworts and mosses along a central Himalayan altitudinal gradient in Nepal (100–5500 m a.s.l.) and to compare these patterns with patterns observed for ferns and flowering plants. We also evaluate the potential importance of Rapoport’s elevational rule in explaining the observed richness patterns for liverworts and mosses. Location Nepal, Central Himalaya. Methods We used published data on the altitudinal ranges of over 840 Nepalese mosses and liverworts to interpolate presence between maximum and minimum recorded elevations, thereby giving estimates of species richness for 100‐m altitudinal bands. These were compared with previously published patterns for ferns and flowering plants, derived in the same way. Rapoport’s elevational rule was assessed by correlation analyses and the statistical significance of the observed correlations was evaluated by Monte Carlo simulations. Results There are strong correlations between richness of the four groups of plants. A humped, unimodal relationship between species richness and altitude was observed for both liverworts and mosses, with maximum richness at 2800 m and 2500 m, respectively. These peaks contrast with the richness peak of ferns at 1900 m and of vascular plants, which have a plateau in species richness between 1500 and 2500 m. Endemic liverworts have their maximum richness at 3300 m, whereas non‐endemic liverworts show their maximum richness at 2700 m. The proportion of endemic species is highest at about 4250 m. There is no support from Nepalese mosses for Rapoport’s elevational rule. Despite a high correlation between altitude and elevational range for Nepalese liverworts, results from null simulation models suggest that no clear conclusions can be made about whether liverworts support Rapoport’s elevational rule. Main conclusions Different demands for climatic variables such as available energy and water may be the main reason for the differences between the observed patterns for the four plant groups. The mid‐domain effect may explain part of the observed pattern in moss and liverwort richness but it probably only works as a modifier of the main underlying relationship between climate and species richness.     

Latitudinal and altitudinal patterns of plant community diversity on mountain summits across the tropical Andes

The high tropical Andes host one of the richest alpine floras of the world, with exceptionally high levels of endemism and turnover rates. Yet, little is known about the patterns and processes that structure altitudinal and latitudinal variation in plant community diversity. Herein we present the first continental‐scale comparative study of plant community diversity on summits of the tropical Andes. Data were obtained from 792 permanent vegetation plots (1 m²) within 50 summits, distributed along a 4200 km transect; summit elevations ranged between 3220 and 5498 m a.s.l. We analyzed the plant community data to assess: 1) differences in species abundance patterns in summits across the region, 2) the role of geographic distance in explaining floristic similarity and 3) the importance of altitudinal and latitudinal environmental gradients in explaining plant community composition and richness. On the basis of species abundance patterns, our summit communities were separated into two major groups: Puna and Páramo. Floristic similarity declined with increasing geographic distance between study‐sites, the correlation being stronger in the more insular Páramo than in the Puna (corresponding to higher species turnover rates within the Páramo). Ordination analysis (CCA) showed that precipitation, maximum temperature and rock cover were the strongest predictors of community similarity across all summits. Generalized linear model (GLM) quasi‐Poisson regression indicated that across all summits species richness increased with maximum air temperature and above‐ground necromass and decreased on summits where scree was the dominant substrate. Our results point to different environmental variables as key factors for explaining vertical and latitudinal species turnover and species richness patterns on high Andean summits, offering a powerful tool to detect contrasting latitudinal and altitudinal effects of climate change across the tropical Andes.     

Environmental and geometric drivers of small mammal diversity along elevational gradients in Utah

The mechanisms shaping patterns of biodiversity along spatial gradients remain poorly known and controversial. Hypotheses have emphasized the importance of both environmental and spatial factors. Much of the uncertainty about the relative role of these processes can be attributed to the limited number of comparative studies that evaluate multiple potential mechanisms. This study examines the relative importance of six variables: temperature, precipitation, productivity, habitat heterogeneity, area, and the mid-domain effect on patterns of species richness for non-volant small mammals along four neighboring mountain ranges in central Utah. Along each of these elevational gradients, a hump-shaped relationship of richness with elevation is evident. This study evaluates whether the processes shaping this common pattern are also common to all gradients. Model selection indicates that no one factor or set of factors best explains patterns of species richness across all gradients, and drivers of diversity may vary seasonally. These findings suggest that commonality in the pattern of species richness, even among elevational gradients with a similar biogeographic history and fauna, cannot be attributed to a simple universal explanation.     

Harvestman (Arachnida: Opiliones) species distribution along three Neotropical elevational gradients: an alternative rescue effect to explain Rapoport's rule?

Aim Relationships between elevation and litter‐dweller harvestman (Arachnida: Opiliones) species richness along three elevational gradients in the Brazilian Atlantic Forest were evaluated. Specifically, three candidate explanatory factors for the observed patterns were tested: (1) the mid‐domain effect, (2) the Rapoport effect, and (3) the influence of environmental variables on species density and specimen abundance. Location Cuscuzeiro, Corcovado and Capricórnio mountains, in Ubatuba (23°26′ S, 45°04′ W), a coastal municipality in São Paulo state, south‐eastern Brazil. Methods We recorded harvestman species and abundance through active sampling using 8 × 8‐m plots in both summer and winter. At each plot we measured the temperature, humidity and mean litter depth. Harvestman species richness per elevational band was the sum of all species recorded in each band, plus the species supposed to occur due to the interpolation of the upper and lower elevational records. Differences between observed and expected species richness per elevational band, based on the mid‐domain effect, were examined through a Monte Carlo simulation. The Rapoport effect was evaluated using both the midpoint method and a new procedure proposed here, the ‘specimen method’. We applied multiple regression analysis to evaluate the contribution of each environmental variable (elevation, temperature, humidity and litter depth) on species density and specimen abundance per plot. Results Harvestman abundance and species richness decreased at higher elevations in the three mountains. The decrease in species richness was not monotonic and showed a plateau of high species richness at lower elevations. The number of harvestman species per elevational band does not fit that predicted by the mid‐domain effect based solely on geometric constraints assuming hard boundaries. Species with their midpoints at higher elevations tended to cover broader elevational range sizes. Both the midpoint method and the specimen method detected evidence of the Rapoport effect in the data. At fine spatial scales, temperature and humidity had positive effects on species density and specimen abundance, while mean litter depth had no clear effect. These relationships, however, were not constant between seasons. Main conclusions Our results suggest that harvestman species density declines at higher elevations due to restrictions imposed by temperature and humidity. We found a pattern in species range distribution as predicted by the elevational Rapoport effect. However, the usual rescue effect proposed to explain the Rapoport effect does not apply in our study. Since the majority of harvestman species covering broader elevational ranges do not exhibit reduced abundance at low elevations, an alternative rescue effect is proposed here. According to this alternative rescue effect, the decrease in species richness at higher elevations occurs due to differential upper limits of species with source populations below mid‐elevations. The seasonal differences in the relationships between environmental variables and species richness/specimen abundance per plot is an indication that species occurrence on elevational gradients is seasonally dependent. Thus relationships and hypotheses based on data recorded over short time periods, or in a single season, should be viewed cautiously.     

Elevational gradients and species richness: do methods change pattern perception?

Aim Species richness patterns along elevational gradients have been documented extensively. Yet, the implications of differences in how the data are compiled are seldom explored. We investigate the effect of grain size on the richness–elevation relationship. Grain size varies among the principal methods used to collect or aggregate species occurrences: localized sites, elevational ‘bins’ and interpolation of species ranges. Assumptions of sampling and species distributions also vary among these methods. Methodology can influence the pattern that is perceived and comparability of results. We compare patterns from all three methods explicitly using the same suite of observations, based on museum records and field surveys of non‐flying small mammals. Our assessment is enhanced by comparing patterns resulting from each method for each of six adjacent mountain ranges. Location Utah, North America. Methods We document elevational species richness patterns using generalized linear models (GLMs), comparing the general shape of the trend as well as curvature, location and magnitude of peak richness across methods, both within and among gradients. We also introduce a new procedure to test for richness peaks using site‐based occurrences. Results We find a general congruence of the richness–elevation relationship, depicting a hump‐shaped pattern with a second‐order polynomial GLM showing a significant fit to nearly all gradient‐methodology combinations. However, underlying characteristics of the trend may vary with grain size. As grain size coarsens, maximum species richness increases and elevation of the mode slightly decreases. Results for curvature vary, but degree of curvature tends to increase as grain size coarsens. The richness–elevation patterns are independent of sampling effects. Main conclusions The perceived elevational diversity pattern for small mammals along these mountain ranges is not scale‐dependent. Differences in how the data are compiled are not reflected in major differences in patterns, even when local samples are neither uniformly spaced nor sampled with the same intensity. This result lends confidence to the assertion that patterns documented in similar studies with different methodologies and for which sampling is sufficiently comprehensive are good indicators of diversity. However, consistency of results from more than one compilation method may help to address issues of scale‐dependence, more so when these comparisons are made explicit.     

Explaining Andean megadiversity: the evolutionary and ecological causes of glassfrog elevational richness patterns

The Tropical Andes are an important global biodiversity hotspot, harbouring extraordinarily high richness and endemism. Although elevational richness and speciation have been studied independently in some Andean groups, the evolutionary and ecological processes that explain elevational richness patterns in the Andes have not been analysed together. Herein, we elucidate the processes underlying Andean richness patterns using glassfrogs (Centrolenidae) as a model system. Glassfrogs show the widespread mid‐elevation diversity peak for both local and regional richness. Remarkably, these patterns are explained by greater time (montane museum) rather than faster speciation at mid‐elevations (montane species pump), despite the recency of the major Andean uplift. We also show for the first time that rates of climatic‐niche evolution and elevational change are related, supporting the hypothesis that climatic‐niche conservatism decelerates species' shifts in elevational distributions and underlies the mid‐elevation richness peak. These results may be relevant to other Andean clades and montane systems globally.     

Latitudinal and altitudinal diversity patterns and Rapoport effects in north-west European land snails and their causes

The latitudinal and altitudinal range sizes of north-west European land-snail species increase with increasing latitude/altitude. These Rapoport effects are not caused by northern/high-altitude species with wider latitudinal/altitudinal ranges and southern/low-altitude species with narrower latitudinal/altitudinal ranges, as predicted by the climatic variability hypothesis. They are instead caused mainly by different northern/upper borders of species occurring in the south part of the study area or at low and intermediate altitudes, respectively. This pattern indicates that the observed Rapoport effects are the result mainly of differential northward/upward expansion of species that were restricted to southern/low or intermediate altitude refugia during the glacials. Although all species occurring in a refugium experienced the same climatic conditions, there is stochastic variation in their climatic tolerance. Species with broader climatic tolerance were able to expand farer northwards/upwards postglacial. The altitudinal distribution of species richness in the analysed alpine faunas cannot be explained by the Rapoport-rescue hypothesis, because species richness peaks at intermediate altitudes and because there is no negative correlation between the number of range borders and altitude. The Rapoport-rescue hypothesis alone is probably also insufficient to explain the decrease in species richness with increasing latitude.  © 2006 The Linnean Society of London, Biological Journal of the Linnean Society , 2006, 87 , 309–323.     

Are there latitudinal and altidudinal Rapoport effects in the geographic ranges of Andean passerine birds?

We analysed the range-sizes of 835 Andean passerine species (including 414 endemics and 421 non-endemics) to test for latitudinal and altitudinal Rapoport effects (LRE and ARE). We tested for positive range-size: latitude/altitude correlations using three different methods: (i) Rohde's mid-point method, (ii) species sorted out by altitude, and (iii) a phylogenetic comparative method (CAIC). Using Rohde's mid-point method, the mean latitudinal extent of species does not follow a Rapoport pattern, but the mean latitudinal occupancy of all passerines and non-endemics do increase with latitude. The latitudinal ranges of endemics sorted out by altitude follow a reverse Rapoport effect, but non-endemics support the pattern. CAIC confirms the latitudinal increase in the occupancy of non-endemics, but regressions have low coefficients of determination. The ARE is supported by the mean altitudinal extent of species, but the trend vanishes when controlling for geometric effects. Low-altitude species occupy about the same proportion of the available altitudinal space as do high-altitude ones. Our analyses suggest that latitude and altitude have low explanatory power for understanding the spatial variation in range-sizes at a continental scale. We show how different patterns can emerge from applying different criteria to the analysis of data.     

Elevational gradients of diversity for lizards and snakes in the Hengduan Mountains,China

Comparing elevational gradients across a wide spectrum of climatic zones offers an ideal system for testing hypotheses explaining the altitudinal gradients of biodiversity. We document elevational patterns of lizard and snake species richness, and explore how land area and climatic factors may affect species distributions of lizards and snakes. Our synthesis found 42 lizard species and 94 snake species known from the Hengduan Mountains. The lizards are distributed between 500 and 3500 m, and the snakes are distributed between 500 and 4320 m. The relationship between species richness and elevation for lizards and snakes is unimodal. Land area explains a significant amount of the variation in lizard and snake species richness. The cluster analysis reveals pronounced distinct assemblages for lizards and snakes to better reflect the vertical profiles of climate in the mountains. Climatic variables are strongly associated with lizard and snake richness along the elevational gradient. The data strongly implicate water availability as a key constraint on lizard species richness, and annual potential evapotranspiration is the best predictor of snake species richness along the elevational gradient in the Hengduan Mountains.     

What drives the species richness patterns of non‐volant small mammals along a subtropical elevational gradient?

The biodiversity of non‐volant small mammals along an extensive subtropical elevational gradient was studied for the first time on Gongga Mountain, the highest mountain in Hengduan Mountain ranges in China, located in one of the 25 global biodiversity hotspots. Non‐volant small mammals were replicate sampled in two seasons at eight sampling sites between 1000 and 4200 m elevation on the eastern slope of Gongga Mountain. In all, 726 individual small mammals representing 25 species were documented in 28 800 trap nights. The species richness pattern for non‐volant small mammals along the elevational gradients was hump‐shaped with highest richness at mid‐elevations. However, different richness patterns emerged between endemic and non‐endemic species, between larger‐ranged and smaller‐ranged species and between rodents and insectivores. Temperature, precipitation, plant species richness and geometric constraints (mid‐ domain effect) were most significant in explaining species richness patterns. Based on the analysis of simple ordinary least squares (OLS) and stepwise multiple regressions, the overall richness pattern, as well as the pattern of insectivores, endemic species and larger‐ranged species showed strong correlation with geometric constraint predictions. However, non‐endemic species richness was more strongly correlated with temperature, while rodent richness was correlated with plant species richness. Our study shows that no single key factor can explain all richness patterns of non‐volant small mammals. We need to be cautious in summarizing a general richness pattern of large species groups (e.g. small mammals or mammals) from species in smaller groups having different ecological distributions and life histories. Elevational richness patterns and their driving factors for small mammals are more likely dependent on what kind of species we study.     

Community of small mammals along an elevational gradient in Biological Reserve of Serra do Japi,municipality of Jundiaí‐SP,Brazil

Studies of elevational gradients in forests are particularly interesting for the considerable differences that can be observed over short distances, such as in vegetation and temperature. Different taxonomic groups display varying types of distribution patterns along elevational gradients, with unimodal distribution being recognised as the most common pattern. The distribution of species can be affected by a range of factors that include, biotic, spatial, climatic, historic and energetic. Small mammals represent an ideal model for studies about distribution and habitat use as they can be highly abundant, tend to have different diets and use space differently. The aims of this study are to build a comprehensive understanding of the community of small mammals of the Biological Reserve of Serra do Japi and to explore its distribution pattern along elevational gradients. We investigated the influence of biomass of arthropods, fruits and seeds and percentage of ground cover, canopy cover and vertical vegetation at richness and abundance of small mammals at three different elevations. To accomplish this, we used seventy‐two pitfall traps of 63 L to capture small mammals and distributed them equally across three elevations defined as low (880–899 m), intermediate (1046–1089 m) and high (1170–1189 m). Each elevation had three lines or replicas of traps. Throughout the study, we captured one hundred and fourteen individuals belonging to eleven species of small mammals. The presence of rare and endemic species demonstrates the importance of conservation and maintenance of the Biological Reserve of Serra do Japi. In regard to the distribution of species, despite the short gradient range, we found a unimodal pattern and a positive correlation between ground cover (fallen twigs and branches up to 1 m high) and richness and abundance of small mammals. More ground cover can reduce the effects of competition and predation on small mammals’ communities. Abstract in Portuguese is available with online material.     

Plant invasion and speciation along elevational gradients on the oceanic island La Palma,Canary Islands

Ecosystems that provide environmental opportunities but are poor in species and functional richness generally support speciation as well as invasion processes. These processes are expected not to be equally effective along elevational gradients due to specific ecological, spatial, and anthropogenic filters, thus controlling the dispersal and establishment of species. Here, we investigate speciation and invasion processes along elevational gradients. We assess the vascular plant species richness as well as the number and percentage of endemic species and non‐native species systematically along three elevational gradients covering large parts of the climatic range of La Palma, Canary Islands. Species richness was negatively correlated with elevation, while the percentage of Canary endemic species showed a positive relationship. However, the percentage of Canary–Madeira endemics did not show a relationship with elevation. Non‐native species richness (indicating invasion) peaked at 500 m elevation and showed a consistent decline until about 1,200 m elevation. Above that limit, no non‐native species were present in the studied elevational gradients. Ecological, anthropogenic, and spatial filters control richness, diversification, and invasion with elevation. With increase in elevation, richness decreases due to species–area relationships. Ecological limitations of native ruderal species related to anthropogenic pressure are in line with the absence of non‐native species from high elevations indicating directional ecological filtering. Increase in ecological isolation with elevation drives diversification and thus increased percentages of Canary endemics. The best preserved eastern transect, including mature laurel forests, is an exception. The high percentage of Canary–Madeira endemics indicates the cloud forest's environmental uniqueness—and thus ecological isolation—beyond the Macaronesian islands.     

Distribution of vascular plant species richness and endemic richness along the Himalayan elevation gradient in Nepal

Aim Species richness and endemic richness vary along elevation gradients, but not necessarily in the same way. This study tests if the maxima in gamma diversity for flowering plants and the endemic subset of these plants are coherent or not. Location The study was conducted in Nepal, between 1000 and 5000 m a.s.l. Methods We used published data on distribution and elevational ranges of the Nepalese flora to interpolate presence between maximum and minimum elevations. Correlation, regression and graphical analyses were used to evaluate the diversity pattern between 1000 and 5000 m a.s.l. Results The interval of maximum species endemic to Nepal or the Himalayas (3800–4200 m) is above the interval of maximum richness (1500–2500 m). The exact location of maximum species density is uncertain and its accuracy depends on ecologically sound estimates of area in the elevation zones. There is no positive statistically significant correlation between log‐area and richness (total or endemic). Total richness is positively correlated with log‐area‐adjusted, i.e. estimated area adjusted for the degree of topographic heterogeneity. The proportion of endemic species increases steadily from low to high elevations. The peak in endemism (c. 4000 m) corresponds to the start of a rapid decrease in species richness above 4000 m. This may relate to the last glacial maximum (equilibrium line at c. 4000 m) that penetrated down to 2500–3000 m. This dynamic hard boundary may have caused an increase in the extinction rate above 4000 m, and enhanced the probability of isolation and facilitated speciation of neoendemics, especially among genera with a high proportion of polyploids. Main conclusions The results reject the idea of corresponding maxima in endemic species and species richness in the lowlands tentatively deduced from Stevens’ elevational Rapoport effect. They confirm predictions based on hard boundary theory, but hard‐boundaries should be viewed as dynamic rather than static when broad‐scale biogeographical patterns with a historical component are being interpreted.