Jonathan M Chase

German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig | iDiv · Biodiversity Synthesis

There is little consensus about how natural (e.g. productivity, disturbance) and anthropogenic (e.g. invasive species, habitat destruction) ecological drivers influence biodiversity. Here, we show that when sampling is standardised by area (species density) or individuals (rarefied species richness), the measured effect sizes depend critically on t...

Although invasive plant species often reduce diversity, they rarely cause plant extinctions. We surveyed paired invaded and uninvaded plant communities from three biomes. We reconcile the discrepancy in diversity loss from invaders by showing that invaded communities have lower local richness but steeper species accumulation with area than that of...

Deterministic theories in community ecology suggest that local, niche-based processes, such as environmental filtering, biotic interactions and interspecific trade-offs largely determine patterns of species diversity and composition. In contrast, more stochastic theories emphasize the importance of chance colonization, random extinction and ecologi...

Net primary productivity is a principal driver of biodiversity; large-scale regions with higher productivity generally have more species. This pattern emerges because β-diversity (compositional variation across local sites) increases with productivity, but the mechanisms underlying this phenomenon are unknown. Using data from a long-term experiment...

There remains considerable doubt, debate, and confusion regarding how biodiversity responds to gradients of important environmental drivers, such as habitat size, resource productivity, and disturbance. Here we develop a simple but comprehensive theoretical framework based on competition–colonization multispecies communities to examine the separate...

Motivation: Freshwater ecosystems have been heavily impacted by land-use changes, but syntheses on the impacts on freshwater ecosystems are still limited. Here, we compiled a global database encompassing 248 studies with species abundance data (from multiple taxon groups and geographic locations) across sites with different land-use categories. Thi...

Ecological stability is a vital component of natural ecosystems that can inform effective conservation and ecosystem management. Furthermore, there is increasing interest in making comparisons of stability values across sites, systems and taxonomic groups, often using comparative synthetic approaches, such as meta‐analysis. However, these synthetic...

Conspecific negative density dependence (CNDD) is thought to be a key process in maintaining plant diversity. However, the strength of CNDD is highly variable in space and time as well as among species, and correlates of this variation that might help to understand and explain it remain largely unquantified. Using Bayesian hierarchical models, we t...

Microbial communities can be found nearly everywhere on Earth, from within our own intestines to lakes and soil. These microbiomes are dynamic and sensitive to environmental disturbances, which are only becoming more common as t he impact of human activity grows. To better understand exactly how microbiomes in different environments respond to disr...

Anthropogenic habitat destruction leads to habitat loss and fragmentation, both of which interact to determine how biodiversity changes at the landscape level. While the detrimental effects of habitat loss are clear, there is a long-standing debate about the role of habitat fragmentation per se. We identify the influence of the total habitat amount...

Spatial and trophic processes profoundly influence biodiversity, yet ecological theories often treat them independently. The theory of island biogeography and related theories on metacommunities predict higher species richness with increasing area across islands or habitat patches. In contrast, food-web theory explores the effects of traits and net...

Theory links dispersal and diversity, predicting the highest diversity at intermediate dispersal levels. However, the modulation of this relationship by macro-eco-evolutionary mechanisms and competition within a landscape is still elusive. We examine the interplay between dispersal, competition and landscape structure in shaping biodiversity over 5...

Background Disturbances alter the diversity and composition of microbial communities. Yet a generalized empirical assessment of microbiome responses to disturbance across different environments is needed to understand the factors driving microbiome recovery, and the role of the environment in driving these patterns. Results To this end, we combine...

Herbivorous insects consume a large proportion of the energy flow in terrestrial ecosystems and play a major role in the dynamics of plant populations and communities. However, high-resolution, quantitative predictions of the global patterns of insect herbivory and their potential underlying drivers remain elusive. Here, we compiled and analyzed a...

Ongoing habitat loss and fragmentation caused by human activities represent one of the greatest causes of biodiversity loss. However, the effects of habitat loss and fragmentation are not felt equally among species. Here, we examined how habitat loss influenced the diversity and abundance of species from different trophic levels, with different tra...

Plant diversity decline under nutrient addition in local grassland communities is typically ascribed to the loss of rare species, species with particular traits ill-suited for high nutrient levels, and displacement of many localized species with a few widespread species. Whether these changes result in stronger diversity decline and vegetation homo...

Although native species diversity is frequently reported to enhance invasion resistance, within‐species diversity of native plants can also moderate invasions. While the positive diversity–invasion resistance relationship is often attributed to competition, indirect effects mediated through plant–soil feedbacks can also influence the relationship....

It is commonly thought that the biodiversity crisis includes widespread declines in the spatial variation of species composition, called biotic homogenization. Using a typology relating homogenization and differentiation to local and regional diversity changes, we synthesize patterns across 461 metacommunities surveyed for 10 to 91 years, and 64 sp...

Herbivorous insects consume a large proportion of the energy flow in terrestrial ecosystems and play a major role in the dynamics of plant populations and communities. However, high-resolution, quantitative predictions of the global patterns of insect herbivory and their potential underlying drivers remain elusive. Here, we compiled and analyzed a...

Studies have reported widespread declines in terrestrial insect abundances in recent years1–4, but trends in other biodiversity metrics are less clear-cut5–7. Here we examined long-term trends in 923 terrestrial insect assemblages monitored in 106 studies, and found concomitant declines in abundance and species richness. For studies that were resol...

Human activities continue to create land-use/land-cover (LULC) change across the Earth's surface, and together with climate change, are major drivers of changes in biodiversity through time. However, the impacts of these spatiotemporally variable drivers on biodiversity change can be complex. We examined the effects of interactions between climate...

Background Disturbances alter the diversity and composition of microbial communities. Yet a generalized empirical assessment of microbiome responses to disturbance across different environments is needed to understand the factors driving microbiome recovery, and the role of the environment in driving these patterns. Results To this end we combined...

The island species–area relationship (ISAR) describes how species richness increases with increasing area of a given island or island‐like habitat, such as freshwater lakes. While the ISAR is one of the most common phenomena observed in ecology, there is variation in both the form of the relationship and its underlying mechanisms. We compiled a glo...

The island species–area relationship (SAR) describes how the number of species on an island varies with its area and provides important information about the maintenance of species diversity and how species might be lost as habitats are lost and fragmented. While the island SAR has been widely studied among macroorganisms, patterns for soil microbe...

Anthropogenic habitat modification is a leading contributor to biodiversity change, but it is unclear what factors, including scale, influence the magnitude of change. Changes in species richness and its scaling relationship across an anthropogenic gradient can be influenced by changes in the total number of individuals in each sample, the species...

There is considerable interest in understanding patterns of β-diversity that measure the amount of change in species composition through space or time. Most hypotheses for β-diversity evoke nonrandom processes that generate spatial and temporal within species aggregation; however, β-diversity can also be driven by random sampling processes. Here, w...

Biotic responses to global change include directional shifts in organismal traits. Body size, an integrative trait that determines demographic rates and ecosystem functions, is thought to be shrinking in the Anthropocene. Here, we assessed the prevalence of body size change in six taxon groups across 5025 assemblage time series spanning 1960 to 202...

The rate and extent of global biodiversity change is surpassing our ability to measure, monitor and forecast trends. We propose an interconnected worldwide system of observation networks — a global biodiversity observing system (GBiOS) — to coordinate monitoring worldwide and inform action to reach international biodiversity targets.

Global change alters the stability of biological communities by affecting species richness and how species covary through time (i.e., synchrony). There are few large-scale empirical tests of stability-diversity-synchrony relationships and those mostly focus on the terrestrial realm. Moreover, the effect of synchrony is largely unknown when species...

Linking species traits with the variation in species assemblages across habitats has often proved useful for developing a more mechanistic understanding of species distributions in metacommunities. However, summarizing the rich tapestry of a species in all of its nuance with a few key ecological traits can also lead to an abstraction that provides...

Advances in restoration ecology are needed to guide ecological restoration in a variable and changing world. Coexistence theory provides a framework for how variability in environmental conditions and species interactions affects species success. Here, we conceptually link coexistence theory and restoration ecology. First, including low-density gro...

The causes of biodiversity change are of great scientific interest and central to policy efforts aimed at meeting biodiversity targets. Changes in species diversity and high rates of compositional turnover have been reported worldwide. In many cases, trends in biodiversity are detected, but these trends are rarely causally attributed to possible dr...

Estimating biodiversity change across the planet in the context of widespread human modification is a critical challenge. Here, we review how biodiversity has changed in recent decades across scales and taxonomic groups, focusing on four diversity metrics: species richness, temporal turnover, spatial beta-diversity and abundance. At local scales, c...

While human activities are known to elicit rapid turnover in species composition through time, the properties of the species that increase or decrease their spatial occupancy underlying this turnover are less clear. Here, we used an extensive dataset of 238 metacommunity time series of multiple taxa spread across the globe to evaluate whether speci...

Islands have long been recognized as distinctive evolutionary arenas leading to morphologically divergent species, such as dwarfs and giants. We assessed how body size evolution in island mammals may have exacerbated their vulnerability, as well as how human arrival has contributed to their past and ongoing extinctions, by integrating data on 1231...

Ecologists routinely use statistical models to detect and explain interactions among ecological drivers, with a goal to evaluate whether an effect of interest changes in sign or magnitude in different contexts. Two fundamental properties of interactions are often overlooked during the process of hypothesising, visualising and interpreting interacti...

Geodiversity - the abiotic heterogeneity of Earth's (sub)surface - is gaining recognition for its ecological links to biodiversity. However, theoretical and conceptual knowledge of geodiversity-trait diversity relationships is currently lacking and can improve understanding of abiotic drivers of community assembly. Here we synthesise the state of k...

Human impacts have led to dramatic biodiversity change which can be highly scale‐dependent across space and time. A primary means to manage these changes is via passive (here, the removal of disturbance) or active (management interventions) ecological restoration. The recovery of biodiversity, following the removal of disturbance, is often incomple...

Biotic responses to global change include directional shifts in organismal traits. Body size, an integrative trait that determines demographic rates and ecosystem functions, is often thought to be shrinking in the Anthropocene. Here, we assess the prevalence of body size change in six taxon groups across 5,032 assemblage time-series spanning 1960-2...

Widespread evidence shows that local species richness (α-diversity) loss hampers the biomass production and stability of ecosystems. β-Diversity, namely the variation of species compositions among different ecological communities, represents another important biodiversity component, but studies on how it drives ecosystem functioning show mixed resu...

The species–area relationship (SAR) has over a 150‐year‐long history in ecology, but how its shape and origins vary across scales and organisms remains incompletely understood. This is the first subcontinental freshwater study to examine both these properties of the SAR in a spatially explicit way across major organismal groups (diatoms, insects, a...

Global change drivers, such as anthropogenic nutrient inputs, are increasing globally. Nutrient deposition simultaneously alters plant biodiversity, species composition and ecosystem processes like aboveground biomass production. These changes are underpinned by species extinction, colonisation and shifting relative abundance. Here, we use the Pric...

Our goal is to mobilize global species abundance and assemblage information, via a dedicated and openly accessible data repository and web portal. Preservation of raw observational data is a complement to the modelled geographic projections that are the focus of related projects such as the EBV Data Portal, which provides access to EBV (Essential B...

Biodiversity metrics often integrate data on the presence and abundance of multiple species. Yet our understanding of covariation between changes to the numbers of individuals, the evenness of species relative abundances, and the total number of species remains limited. Using individual‐based rarefaction curves, we show how expected positive relati...

Ecological thresholds comprise relatively fast changes in ecological conditions, with respect to time or external drivers, and are an attractive concept in both scientific and policy arenas. However, there is considerable debate concerning the existence, underlying mechanisms, and generalizability of ecological thresholds across a range of ecologic...

Patterns of biodiversity provide insights into the processes that shape biological communities around the world. Variation in species diversity along biogeographical or ecological gradients, such as latitude or precipitation, can be attributed to variation in different components of biodiversity: changes in the total abundance (i.e., more-individua...

Species abundances and distributions are changing in response to changing climate and other anthropogenic drivers but how this translates into how well species can match their optimal climate conditions as they change is not well understood. Using a continental-scale 30-year time series, we quantified temporal trends in climate matching of North Am...

It is commonly thought that the biodiversity crisis includes widespread decreases in the uniqueness of different sites in a landscape (biotic homogenization). Using a typology relating homogenization and differentiation to local and regional diversity changes, we synthesize patterns across 283 metacommunities surveyed for 10-91 years, and 54 specie...

The same features that generate biodiversity patterns across and within oceanic islands over evolutionary time - interactions between isolation, area, and heterogeneity - also influence their vulnerability to biological invasions. Here, we identify the factors that shape the richness and abundance of woody aliens in forest communities across the Ha...

Global change drivers such as anthropogenic nutrient inputs simultaneously alter biodiversity, species composition, and ecosystem functions such as aboveground biomass. These changes are interconnected by complex feedbacks among extinction, colonization, and shifting relative abundance. Here, we use a novel temporal application of the Price equatio...

Patterns of biodiversity provide insights into the processes that shape biological communities around the world. Variation in species diversity along biogeographical or ecological gradients, such as latitude or precipitation, can be attributed to variation in different components of biodiversity: changes in the total abundance (i.e. more-individual...

Patterns of biodiversity provide insights into the processes that shape biological communities around the world. Variation in species diversity along biogeographical or ecological gradients, such as latitude or precipitation, can be attributed to variation in different components of biodiversity: changes in the total abundance (i.e. more-individual...

In metacommunity ecology, a major focus has been on combining observational and analytical approaches to identify the role of critical assembly processes, such as dispersal limitation and environmental filtering, but this work has largely ignored temporal community dynamics. Here, we develop a “virtual ecologist” approach to evaluate assembly proce...

Broad‐scale biodiversity monitoring relies, at least in part, on the efforts of citizen, or community, scientists. To ensure robust inferences from citizen science data, it is important to understand the spatial pattern of sampling effort by citizen scientists and how it deviates from an optimal pattern. Here, we develop a generalized workflow to e...

1. Human impacts have led to dramatic biodiversity change which can be highly scale-dependent across space and time. A primary means to manage these changes is via passive or active ecological restoration. The recovery of biodiversity following the removal of disturbance (passive) is often incomplete. The magnitude of recovery can very much depend...

Variables describing the abiotic environment (e.g. climate, topography or biogeographic history) have a long tradition of use as predictors of tree species richness patterns. However, these variables may capture variations in richness related to climate, but not those that are related to soil type or forest disturbance. Canopy structure has previou...

1.Estimates of temporal change of biodiversity, and its components loss and gain, are needed at local and geographical scales. However, we lack them because of data in-completeness, heterogeneity, and lack of temporal replication. Hence, we need a tool to integrate heterogeneous data and to account for their incompleteness.2.We introduce spatiotemp...

Aim The abundances and distributions of some species are more closely matched to variations in climate than others. Species traits that might influence how well the distribution and abundance of a species are matched to climatic variation include life history (e.g., body size and dispersal ability), ecology (e.g., habitat specialization and territo...

Changes in the abundances of animals, such as with the ongoing concern about insect declines, are often assumed to be general across taxa. However, this assumption is largely untested. Here, we used a database of assemblage-wide long-term insect and arachnid monitoring to compare abundance trends among co-occurring pairs of taxa. We show that 60% o...