Asymmetry in species regional dispersal ability and the neutral theory

The neutral assumption that individuals of either the same or different species share exactly the same birth, death, migration, and speciation probabilities is fundamental yet controversial to the neutral theory. Several theoretical studies have demonstrated that a slight difference in species per capita birth or death rates can have a profound consequence on species coexistence and community structure. Whether asymmetry in migration, a vital demographic parameter in the neutral model, plays an important role in community assembly still remains unknown. In this paper, we relaxed the ecological equivalence assumption of the neutral model by introducing differences into species regional dispersal ability. We investigated the effect of asymmetric dispersal on the neutral local community structure. We found that per capita asymmetric dispersal among species could reduce species richness of the local community and result in deviations of species abundance distributions from those predicted by the neutral model. But the effect was moderate compared with that of asymmetries in birth or death rates, unless very large asymmetries in dispersal were assumed. A large difference in species dispersal ability, if there is, can overwhelm the role of random drift and make local community dynamics deterministic. In this case, species with higher regional dispersal abilities tended to dominate in the local community. However, the species abundance distribution of the local community under asymmetric dispersal could be well fitted by the neutral model, but the neutral model generally underestimated the fundamental biodiversity number but overestimated the migration rate in such communities.     

Explaining bird species composition and richness in eucalypt-dominated remnants in subhumid Tasmania

Aim To determine the factors influencing the distribution of birds in remnants in a fragmented agricultural landscape. Location Forty‐seven eucalypt remnants and six sites in continuous forest in the subhumid Midlands region of Tasmania, Australia. Methods Sites were censused over a two‐year period, and environmental data were collected for remnants. The avifauna of the sites was classified and ordinated. The abundances of bird species, and bird species composition, richness, abundance and diversity were related to environmental variables, using simple correlation and modelling. Results There were two distinct groups of sample sites, which sharply differed in species composition, richness, diversity and bird abundance, separated on the presence/absence of noisy miner (Manorina melanocephala Latham) colonies, remnant size, vegetation structural attributes and variables that reflected disturbance history. The approximate remnant size threshold for the change from one group to another was 20–30 ha. Remnant species richness and diversity were most strongly explained by remnant area and noisy miner abundance, with contributions from structural and isolation attributes in the second case. Segment richness was explained by precipitation, logging history and noisy miner abundance. Bird abundance was positively related to precipitation and negatively related to tree dieback. The 28 individual bird species models were highly individualistic, with vegetation structural variables, noisy miner abundance, climatic variables, variables related to isolation, area, variables related to floristics, disturbance variables, the nature of the matrix and remnant shape all being components in declining order of incidence. Age of the remnant did not relate to any of the dependent variables. Main conclusions Degraded and small remnants may have become more distinct in their avifaunal characteristics than might otherwise be the case, as a result of the establishment of colonies of an aggressive native bird, the noisy miner. The area, isolation and shape of remnants directly relate to the abundance of relatively few species, compared to vegetation attributes, climate and the abundance of the noisy miner. The nature of the matrix is important in the response of some species to fragmentation.     

Multi-scale analysis on species diversity within a 40-ha old-growth temperate forest

In order to better explore the maintenance mechanisms of biodiversity,data collected from a 40-ha undisturbed Pinus forest were applied to the Individual SpecieseArea Relationship model (ISAR) to determine distribution patterns for species richness.The ecological processes influencing species abundance distribution patterns were assessed by applying the same data set to five models:a LogNormal Model (LNM),a Broken Stick Model (BSM),a Zipf Model (ZM),a Niche Preemption Model (NPM),and a Neutral Model (NM).Each of the five models was used at six different sampling scales (10 m×10 m,20 m×20 m,40 m×40 m,60 m×60 m,80 m×80 m,and 100 m×100 m).Model outputs showed that:(1) Accumulators and neutral species strongly influenced species diversity,but the relative importance of the two types of species varied across spatial scales.(2) Distribution patterns of species abundance were best explained by the NPM at small scales (10 me20 m),whereas the NM was the best fit model at large spatial scales.(3) Species richness and abundance distribution patterns appeared to be driven by similar ecological processes.At small scales,the niche theory could be applied to describe species richness and abundance,while at larger scales the neutral theory was more applicable.     

Abundance of common species,not species richness,drives delivery of a real‐world ecosystem service

Biodiversity‐ecosystem functioning experiments have established that species richness and composition are both important determinants of ecosystem function in an experimental context. Determining whether this result holds for real‐world ecosystem services has remained elusive, however, largely due to the lack of analytical methods appropriate for large‐scale, associational data. Here, we use a novel analytical approach, the Price equation, to partition the contribution to ecosystem services made by species richness, composition and abundance in four large‐scale data sets on crop pollination by native bees. We found that abundance fluctuations of dominant species drove ecosystem service delivery, whereas richness changes were relatively unimportant because they primarily involved rare species that contributed little to function. Thus, the mechanism behind our results was the skewed species‐abundance distribution. Our finding that a few common species, not species richness, drive ecosystem service delivery could have broad generality given the ubiquity of skewed species‐abundance distributions in nature.     

Random sampling, abundance–extinction dynamics and niche-filtering immigration constraints explain the generation of species richness gradients

Aim  The paradigm that species' patterns of distribution, abundance and coexistence are the result of adaptations of the species to their niches has recently been challenged by evidence that similar patterns may be generated by simple random processes. We argue here that a better understanding of macroecological patterns requires an integration of both ecological and neutral stochastic approaches. We demonstrate the utility of such an integrative approach by testing the sampling hypothesis in a species–energy relationship of forest bird species.
Location  A Mediterranean biome in Catalonia, Spain.
Methods  To test the sampling hypothesis we designed a metacommunity model that reproduces the stochastic sampling from a regional pool to predict local species richness variation. Four conceptually different sampling procedures were evaluated.
Results  We showed that stochastic sampling processes predicted a substantial part (over 40%) of the observed variation in species richness, but left considerable variation unexplained. This remaining variation in species richness may be better understood as the result of alternative ecological processes. First, the sampling model explained more variation in species richness when the probability that a species colonises a new locality was assumed to increase with its niche width, suggesting that ecological differences between species matter when it comes to explaining macroecological patterns. Second, extinction risk was significantly lower for species inhabiting high-energy regions, suggesting that abundance–extinction processes play a significant role in shaping species richness patterns.
Main conclusions  We conclude that species–energy relationships may not simply be understood as a result of either ecological or random sampling processes, but more likely as a combination of both.     

Plant species richness as the main driver of moth metacommunities

1. Ecologists have recognised several factors that may explain the distribution of species in a metacommunity. These factors may be related to the dispersal of individuals among the patches and environmental conditions. 2. Here, we attempted to determine which of the four different metacommunity frameworks (patch dynamics, mass effect, neutral processes, and species sorting) explain the distribution of Arctiinae moths in Brazilian savanna areas with different tree species richness. 3. The Arctiinae moths were categorised as habitat specialists or generalists, common or rare, and belonging to the tribes Arctiini and Lithosiini. We hypothesized that environmental variables best explain the abundance and occurrence of habitat specialist species, common species, and members of Lithosiini; whereas spatial processes are more closely related to habitat generalists, rare species, and members of Arctiini. 4. Contrary to our expectations, we found that the species sorting (mainly dictated by the species richness of trees) best explained the variation in abundance and occurrence of the majority of species groups. Spatial processes (more related to patch dynamics, mass effect, and neutral), although they were significantly related to some species groups, were not strong enough to explain the distribution of these species in the study area. 5. The plant species richness was the most important environmental condition, related to moth species niches. Therefore, species sorting best explained the distribution of the species of Arctiinae in the Brazilian savanna.     

Effect of species richness and relative abundance on the shape of the species accumulation curve

Abstract We explain how species accumulation curves are influenced by species richness (total number of species), relative abundance and diversity using computer‐generated simulations. Species richness defines the boundary of the horizontal asymptote value for a species accumulation curve, and the shape of the curve is influenced by both relative abundance and diversity. Simulations with a high proportion of rare species and a few abundant species have a species accumulation curve with a low ‘shoulder’ (inflection point on the ordinate axis) and a long upward slope to the asymptote. Simulations with a high proportion of relatively abundant species have a steeply rising initial slope to the species accumulation curve and plateau early. Diversity (as measured by Simpson's and Shannon–Weaver indices) for simulations is positively correlated with the initial slope of the species accumulation curve. Species accumulation curves cross when one simulation has a high proportion of both rare and abundant species compared with another that has a more even distribution of abundance among species.     

Non‐neutrality in forest communities: evolutionary and ecological determinants of tree species abundance distributions

The unified neutral theory of biodiversity and biogeography provides a promising framework that can be used to integrate stochastic and ecological processes operating in ecological communities. Based on a mechanistic non‐neutral model that incorporates density‐dependent mortality, we evaluated the deviation from a neutral pattern in tree species abundance distributions and explored the signatures of historical and ecological processes that have shaped forest biomes. We compiled a dataset documenting species abundance distributions in 1168 plots encompassing 16 973 tree species across tropical, temperate, and boreal forests. We tested whether deviations from neutrality of species abundance distributions vary with climatic and historical conditions, and whether these patterns differ among regions. Non‐neutrality in species abundance distributions was ubiquitous in tropical, temperate, and boreal forests, and regional differences in patterns of non‐neutrality were significant between biomes. Species abundance evenness/unevenness caused by negative density‐dependent or abiotic filtering effects had no clear macro‐scale climatic drivers, although temperature was non‐linearly correlated with species abundance unevenness on a global scale. These findings were not significantly biased by heterogeneity of plot data (the differences of plot area, measurement size, species richness, and the number of individuals sampled). Therefore, our results suggest that environmental filtering is not universally increasing from warm tropical to cold boreal forests, but might affect differently tree species assembly between and within biomes. Ecological processes generating particularly dominant species in local communities might be idiosyncratic or region‐specific and may be associated with geography and climate. Our study illustrates that stochastic dynamical models enable the analysis of the interplay of historical and ecological processes that influence community assemblies and the dynamics of biodiversity.     

Effect of local and regional processes on plant species richness in tallgrass prairie

Historically, diversity in a community was often believed to result primarily from local processes, but recent evidence suggests that regional diversity may strongly influence local diversity as well. We used experimental and observational vegetation data from Konza Prairie, Kansas, USA, to determine if: (1) there is a relationship between local and regional richness in tallgrass prairie vegetation; (2) local dominance reduces local species richness; and (3) reducing local dominance increases local and regional species richness. We found a positive relationship between regional and local richness; however, this relationship varied with grazing, topography and fire frequency. The decline in variance explained in the grazed vegetation, in particular, suggested that local processes associated with grazing pressure on the dominant grasses strongly influenced local species richness. Experimental removal of one of the dominant grasses, Andropogon scoparius , from replicate plots resulted in a significant increase in local species richness compared to adjacent reference plots. Overall all sites, species richness was higher in grazed (192 spp.) compared to ungrazed (158 spp.) areas. Across the Konza Prairie landscape, however, there were no significant differences in the frequency distribution of species occurrences, or in the relationship between the number of sites occupied and average abundance in grazed compared to ungrazed areas. Thus, local processes strongly influenced local richness in this tallgrass prairie, but local processes did not produce different landscape-scale patterns in species distribution and abundance. Because richness was enhanced at all spatial scales by reducing the abundance of dominant species, we suggest that species richness in tallgrass prairie results from feedbacks between, and interactions among, processes operating at multiple scales in space and time.     

The decoupling of abundance and species richness in lizard communities

1. Patterns of species richness often correlate strongly with measures of energy. The more individuals hypothesis (MIH) proposes that this relationship is facilitated by greater resources supporting larger populations, which are less likely to become extinct. Hence, the MIH predicts that community abundance and species richness will be positively related. 2. Recently, Buckley & Jetz (2010, Journal of Animal Ecology, 79, 358-365) documented a decoupling of community abundance and species richness in lizard communities in south-west United States, such that richer communities did not contain more individuals. They predicted, as a consequence of the mechanisms driving the decoupling, a more even distribution of species abundances in species-rich communities, evidenced by a positive relationship between species evenness and species richness. 3. We found a similar decoupling of the relationship between abundance and species richness for lizard communities in semi-arid south-eastern Australia. However, we note that a positive relationship between evenness and richness is expected because of the nature of the indices used. We illustrate this mathematically and empirically using data from both sets of lizard communities. When we used a measure of evenness, which is robust to species richness, there was no relationship between evenness and richness in either data set. 4. For lizard communities in both Australia and the United States, species dominance decreased as species richness increased. Further, with the iterative removal of the first, second and third most dominant species from each community, the relationship between abundance and species richness became increasingly more positive. 5. Our data support the contention that species richness in lizard communities is not directly related to the number of individuals an environment can support. We propose an alternative hypothesis regarding how the decoupling of abundance and richness is accommodated; namely, an inverse relationship between species dominance and species richness, possibly because of ecological release.     

Spatial variation of species diversity across scales in an old-growth temperate forest of China

Species richness and abundance are the two most important diversity variables. Species abundance is additive when aggregated across spatial scale, whereas species richness is non-additive. This study analyzes the effect of spatial scale and site on species abundance and richness in a 25-ha temperate forest plot in the Changbai Mountains, northeastern China. The result shows that species abundance and richness are not only dependent on spatial scales, but also dependent on site. Species abundance responds linearly to changes of spatial scale with no intersection in different sites of the study area. However, although species richness also increases with the increase of spatial scale, there are some intersections for the different sites, suggesting that a species-rich site does not always have a high value if the spatial scale is changed. In all, with respect to additive variables, it is relatively easy to extrapolate them from one spatial scale to another spatial scale, as they and the spatial scale usually form a linear relationship. In contrast, non-additive variables are difficult to extrapolate across spatial scales, because they often respond nonlinearly to spatial scale changes. In order to extrapolate these non-additive variables across spatial scales, it is necessary to estimate the relationships between them and spatial scales. As a result, extrapolation of information among spatial scales may be possible, but very difficult, especially for non-additive variables. Because the 25-ha Changbai plot is very small compared to the extent of the world temperate forests, and the vegetation is a relatively uniform type, more such studies in other ecosystems are needed before theories and generalization about scaling effects can be formulated.     

A multivariate model of plant species richness in forested systems: old-growth montane forests with a long history of fire

Recently, efforts to develop multivariate models of plant species richness have been extended to include systems where trees play important roles as overstory elements mediating the influences of environment and disturbance on understory richness. We used structural equation modeling to examine the relationship of understory vascular plant species richness to understory abundance, forest structure, topographic slope, and surface fire history in lower montane forests on the North Rim of Grand Canyon National Park, USA based on data from eighty‐two 0.1 ha plots. The questions of primary interest in this analysis were: (1) to what degree are influences of trees on understory richness mediated by effects on understory abundance? (2) To what degree are influences of fire history on richness mediated by effects on trees and/or understory abundance? (3) Can the influences of fire history on this system be related simply to time‐since‐fire or are there unique influences associated with long‐term fire frequency? The results we obtained are consistent with the following inferences. First, it appears that pine trees had a strong inhibitory effect on the abundance of understory plants, which in turn led to lower understory species richness. Second, richness declined over time since the last fire. This pattern appears to result from several processes, including (1) a post‐fire stimulation of germination, (2) a decline in understory abundance, and (3) an increase over time in pine abundance (which indirectly leads to reduced richness). Finally, once time‐since‐fire was statistically controlled, it was seen that areas with higher fire frequency have lower richness than expected, which appears to result from negative effects on understory abundance, possibly by depletions of soil nutrients from repeated surface fire. Overall, it appears that at large temporal and spatial scales, surface fire plays an important and complex role in structuring understory plant communities in old‐growth montane forests. These results show how multivariate models of herbaceous richness can be expanded to apply to forested systems.     

Plant species richness in continental southern Siberia: effects of pH and climate in the context of the species pool hypothesis

Aim Many high‐latitude floras contain more calcicole than calcifuge vascular plant species. The species pool hypothesis explains this pattern through an historical abundance of high‐pH soils in the Pleistocene and an associated opportunity for the evolutionary accumulation of calcicoles. To obtain insights into the history of calcicole/calcifuge patterns, we studied species richness–pH–climate relationships across a climatic gradient, which included cool and dry landscapes resembling the Pleistocene environments of northern Eurasia. Location Western Sayan Mountains, southern Siberia. Methods Vegetation and environmental variables were sampled at steppe, forest and tundra sites varying in climate and soil pH, which ranged from 3.7 to 8.6. Species richness was related to pH and other variables using linear models and regression trees. Results Species richness is higher in areas with warmer winters and at medium altitudes that are warmer than the mountains and wetter than the lowlands. In treeless vegetation, the species richness–pH relationship is unimodal. In tundra vegetation, which occurs on low‐pH soils, richness increases with pH, but it decreases in steppes, which have high‐pH soils. In forests, where soils are more acidic than in the open landscape, the species richness–pH relationship is monotonic positive. Most species occur on soils with a pH of 6–7. Main conclusions Soil pH in continental southern Siberia is strongly negatively correlated with precipitation, and species richness is determined by the opposite effects of these two variables. Species richness increases with pH until the soil is very dry. In dry soils, pH is high but species richness decreases due to drought stress. Thus, the species richness–pH relationship is unimodal in treeless vegetation. Trees do not grow on the driest soils, which results in a positive species richness–pH relationship in forests. If modern species richness resulted mainly from the species pool effects, it would suggest that historically common habitats had moderate precipitation and slightly acidic to neutral soils.     

Bryozoan assemblages on hard substrata: species abundance distribution and competition for space

Bryozoans are colonial invertebrates that often dominate epibenthic assemblages on the lower surfaces of hard substrata. Competition among neighbouring organisms is usually a critical process regulating biodiversity, and hard substrata have proved to be a suitable model habitat to analyse spatial interactions. We explored the relationships among abundance, species richness, diversity, competitive ability, coverage, available surface, depth and substratum size in an assemblage of bryozoans encrusting pebbles and cobbles in a bank off the eastern mouth of the Strait of Magellan. We also tested whether overgrowth competition can be regarded as hierarchical, and whether the species abundance distribution shows a mode of rare species and a decreasing frequency of increasingly abundant species. Abundance, species richness, diversity and overgrowth competition were highest on the largest substrata. Smaller pebbles tended to be encrusted by the commonest bryozoans, while the rarest species were mainly found on relatively larger clasts. A high proportion of the lower surfaces of most substrata was available for growth. Diversity values of relatively shallow stations were lower than expected under Caswell’s neutral model. Interspecific competition was hierarchical, but the abundance of colonies was not related to the competitive ability of each species. The species abundance distribution was bimodal, with a main mode of rare species and a second one partly composed of relatively abundant bryozoans with poor competitive abilities. This study shows that even in an encrusting assemblage where competition is hierarchical, the weakest competitors persist and the dominant species are far from being capable of monopolizing space.     

Regional‐scale patterns and predictors of species richness and abundance across twelve major tropical inter‐reef taxa

Species richness and abundance are biodiversity metrics widely used to describe and estimate changes in biodiversity. Studies of marine species richness and abundance typically focus on one, or just a few, taxa. Consequently, it is currently not possible to understand the performance of predictors of species richness and abundance across marine taxa. Using a taxonomically comprehensive dataset of twelve major taxa of flora and fauna from eight phyla sampled from the inter‐reef seabed region of the Great Barrier Reef, Australia, we used boosted regression trees to test the performance of fourteen environmental and spatial predictors of species richness and abundance. Sediment composition predicted richness best for all taxa: gravel contributed up to 39% relative influence for one group and all taxa had low richness in muddy habitats. Sea surface temperature, seabed current shear stress, depth and latitude were also influential predictors for species richness for eight groups. Sediment was frequently an influential predictor for abundance also, while distance to domain (reef/coast) and longitude were relatively influential for six taxa. Within‐site richness was correlated between nearly all pairs of taxa, as was within‐site abundance, however ρ values were low. Overall, model performance was high, explaining up to 62% deviance of species richness, and 38% of abundance. Typically, deviance explained was greater for richness than abundance and may indicate that some drivers of species richness operate independently of any effects on species richness mediated by their effect on abundance. Deviance explained differed most between richness and abundance for bryozoans (23.3% difference) and soft corals (15.2% difference). While sediments were consistently the best predictors across all taxa, the inconsistent influence of all other predictors across taxonomic groups, as well as the low correlation of richness and abundance across taxonomic groups, cautions against predicting regional patterns of species richness and abundance from few taxa.     

Mammal density and patterns of ectoparasite species richness and abundance

Patterns of species richness, prevalence and abundance of ectoparasites have rarely been investigated at both the levels of populations and species of hosts. Here, we investigated the effects in changes in small mammal density on species richness, abundance and prevalence of ectoparasitic fleas. The comparative analyses were conducted for different small mammal species and among several populations during a long-term survey. We tested the hypothesis that an increase in host density should be linked with an increase in parasite species richness both among host species and among populations within host species, as predicted by epidemiological models. We also used host species density data from literature. We found that host density has a major influence on the species richness of ectoparasite communities of small mammals among host populations. We found no relationship between data of host density from the literature and parasite species richness. In contrast with epidemiological hypotheses, we found no relationships between abundance, or prevalence, and host density, either among host species or among host populations. Moreover, a decrease in abundance of fleas in relation with an increase in host density was observed for two mammal species (Apodemus agrarius and A. flavicollis). The decrease or the lack of increase in flea abundance in relation with an increase in host density suggests anti-parasitic behavioural activities such as grooming.     

Host abundance,durability, basidiome form and phylogenetic isolation determine fungivore species richness

Species with close associations to a specific host species, such as parasites and phytophages, make immense contributions to biodiversity. Hence, factors determining the variation in species richness among hosts are a main focus of ecological research. Investigations of determining factors of fungivorous species among host species are still scarce. Based on ecological patterns of parasites and phytophages, we hypothesized that the species richness of tree‐fungus beetles of the family Ciidae (Coleoptera) would increase with increasing basidiome size, niche diversity of the growth form, durability, increasing abundance and decreasing phylogenetic isolation of the host fungus. Our generalized least‐squares model, controlled by host phylogeny, revealed that Ciidae species richness increases with host abundance, but decreases with host phylogenetic isolation. In contrast with our prediction, Ciidae species richness was higher in annual basidiomes than in perennials. Pileate basidiomes revealed higher species richness than resupinate and stipitate basidiomes, which may be interpreted as being a result of their higher host niche diversity. The importance of host abundance, measured on the landscape scale, corroborates that fungivore species richness among macrofungal hosts is determined by factors similar to those that determine parasite and phytophage species richness among their hosts. © 2015 The Linnean Society of London, Biological Journal of the Linnean Society, 2015, 114 , 699–708.     

Genotypic diversity of an invasive plant species promotes litter decomposition and associated processes

Following studies that showed negative effects of species loss on ecosystem functioning, newer studies have started to investigate if similar consequences could result from reductions of genetic diversity within species. We tested the influence of genotypic richness and dissimilarity (plots containing one, three, six or 12 genotypes) in stands of the invasive plant Solidago canadensis in China on the decomposition of its leaf litter and associated soil animals over five monthly time intervals. We found that the logarithm of genotypic richness was positively linearly related to mass loss of C, N and P from the litter and to richness and abundance of soil animals on the litter samples. The mixing proportion of litter from two sites, but not genotypic dissimilarity of mixtures, had additional effects on measured variables. The litter diversity effects on soil animals were particularly strong under the most stressful conditions of hot weather in July: at this time richness and abundance of soil animals were higher in 12-genotype litter mixtures than even in the highest corresponding one-genotype litter. The litter diversity effects on decomposition were in part mediated by soil animals: the abundance of Acarina, when used as covariate in the analysis, fully explained the litter diversity effects on mass loss of N and P. Overall, our study shows that high genotypic richness of S. canadensis leaf litter positively affects richness and abundance of soil animals, which in turn accelerate litter decomposition and P release from litter.     

Environmental effects on Neotropical liana species richness

Aim Lianas differ physiologically from trees, and therefore their species‐richness patterns and potential climate‐change responses might also differ. However, multivariate assessments of spatial patterns in liana species richness and their controls are lacking. Our aim in this paper is to identify the environmental factors that best explain the variation in liana species richness within tropical forests. Location Lowland and montane Neotropical forests. Methods We quantified the contributions of environmental variables and liana and tree‐and‐shrub abundance to the species richness of lianas, trees and shrubs ≥ 2.5 cm in diameter using a subset of 65 standardized (0.1 ha) plots from 57 Neotropical sites from a global dataset collected by the late Alwyn Gentry. We used both regression and structural equation modelling to account for the effects of environmental variables (climate, soil and disturbance) and liana density on liana species richness, and we compared the species‐richness patterns of lianas with those of trees and shrubs. Results We found that, after accounting for liana density, dry‐season length was the dominant predictor of liana species richness. In addition, liana species richness was also related to stand‐level wood density (a proxy for disturbance) in lowland forests, a pattern that has not hitherto been shown across such a large study region. Liana species richness had a weak association with soil properties, but the effect of soil may be obscured by the strong correlation between soil properties and climate. The diversity patterns of lianas and of trees and shrubs were congruent: wetter forests had a greater species richness of all woody plants. Main conclusions The primary association of both liana and tree‐and‐shrub species richness with water availability suggests that, if parts of the Neotropics become drier as a result of climate change, substantial declines in the species richness of woody plants at the stand level may be anticipated.     

Grazing and an invasive grass confound spatial pattern of exotic and native grassland plant species richness

Previous work has shown exotic and native plant species richness are negatively correlated at fine spatial scales and positively correlated at broad spatial scales. Grazing and invasive plant species can influence plant species richness, but the effects of these disturbances across spatial scales remain untested. We collected species richness data for both native and exotic plants from five spatial scales (0.5–3000 m²) in a nested, modified Whittaker plot design from severely grazed and ungrazed North American tallgrass prairie. We also recorded the abundance of an abundant invasive grass, tall fescue (Schedonorus phoenix (Scop.) Holub), at the 0.5-m² scale. We used linear mixed-effect regression to test relationships between plant species richness, tall fescue abundance, and grazing history at five spatial scales. At no scale was exotic and native species richness linearly related, but exotic species richness at all scales was greater in grazed tracts than ungrazed tracts. Native species richness declined with increasing tall fescue abundance at all five spatial scales, but exotic species richness increased with tall fescue abundance at all but the broadest spatial scales. Severe grazing did not reduce native species richness at any spatial scale. We posit that invasion of tall fescue in this working landscape of originally native grassland plants modifies species richness-spatial scale relationships observed in less disturbed systems. Tall fescue invasion constitutes a unique biotic effect on plant species richness at broad spatial scales.