Ecology Letters

Papers
(The TQCC of Ecology Letters is 16. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-04-01 to 2024-04-01.)
ArticleCitations
Co‐occurrence is not evidence of ecological interactions426
The effectiveness of flower strips and hedgerows on pest control, pollination services and crop yield: a quantitative synthesis320
AVONET: morphological, ecological and geographical data for all birds284
Designing optimal human‐modified landscapes for forest biodiversity conservation277
A process‐based metacommunity framework linking local and regional scale community ecology191
The effects of livestock grazing on biodiversity are multi‐trophic: a meta‐analysis138
Effect of allelopathy on plant performance: a meta‐analysis133
Uncovering ecological state dynamics with hidden Markov models108
Ecological impacts of human‐induced animal behaviour change102
Soil carbon persistence governed by plant input and mineral protection at regional and global scales98
A global agenda for advancing freshwater biodiversity research97
The worldwide impact of urbanisation on avian functional diversity95
Biotic interactions are more often important at species’ warm versus cool range edges88
Biodiversity promotes ecosystem functioning despite environmental change85
Global trends in phenotypic plasticity of plants81
The context dependence of non‐consumptive predator effects80
Species distribution models have limited spatial transferability for invasive species78
The seventh macronutrient: how sodium shortfall ramifies through populations, food webs and ecosystems76
Functional roles of microbial symbionts in plant cold tolerance76
Plant community composition steers grassland vegetation via soil legacy effects76
A group of ectomycorrhizal fungi restricts organic matter accumulation in boreal forest76
Root‐derived inputs are major contributors to soil carbon in temperate forests, but vary by mycorrhizal type75
Biodiversity loss underlies the dilution effect of biodiversity71
A tipping point in carbon storage when forest expands into tundra is related to mycorrhizal recycling of nitrogen70
Sick plants in grassland communities: a growth‐defense trade‐off is the main driver of fungal pathogen abundance69
Global functional and phylogenetic structure of avian assemblages across elevation and latitude68
We should not necessarily expect positive relationships between biodiversity and ecosystem functioning in observational field data67
Long‐term change in the avifauna of undisturbed Amazonian rainforest: ground‐foraging birds disappear and the baseline shifts65
The dimensionality and structure of species trait spaces64
Winter in water: differential responses and the maintenance of biodiversity64
Tree growth sensitivity to climate is temporally variable63
Quantifying 25 years of disease‐caused declines in Tasmanian devil populations: host density drives spatial pathogen spread63
Seeing through the static: the temporal dimension of plant–animal mutualistic interactions63
Reduced phenotypic plasticity evolves in less predictable environments62
Towards the fully automated monitoring of ecological communities62
Latitudinal patterns of terrestrial phosphorus limitation over the globe62
Floral resource diversification promotes solitary bee reproduction and may offset insecticide effects – evidence from a semi‐field experiment58
Consistently positive effect of species diversity on ecosystem, but not population, temporal stability58
A global analysis of song frequency in passerines provides no support for the acoustic adaptation hypothesis but suggests a role for sexual selection58
The jury is still out regarding the generality of adaptive ‘transgenerational’ effects58
Landscape simplification increases vineyard pest outbreaks and insecticide use57
Adaptation and coordinated evolution of plant hydraulic traits57
Number of growth days and not length of the growth period determines radial stem growth of temperate trees57
High water use in desert plants exposed to extreme heat57
Montane species track rising temperatures better in the tropics than in the temperate zone56
Landscape simplification shapes pathogen prevalence in plant‐pollinator networks56
Trait matching and phenological overlap increase the spatio‐temporal stability and functionality of plant–pollinator interactions56
Intuitive and broadly applicable definitions of niche and fitness differences55
Bee phenology is predicted by climatic variation and functional traits55
Future climate risks from stress, insects and fire across US forests54
Seed size predicts global effects of small mammal seed predation on plant recruitment53
The evolutionary ecology of fatty‐acid variation: Implications for consumer adaptation and diversification53
Dilution effects in disease ecology52
Shape matters: the relationship between cell geometry and diversity in phytoplankton51
Generalising indirect defence and resistance of plants51
Temporal changes in spatial variation: partitioning the extinction and colonisation components of beta diversity50
When do Janzen–Connell effects matter? A phylogenetic meta‐analysis of conspecific negative distance and density dependence experiments49
Smaller adult fish size in warmer water is not explained by elevated metabolism49
Field‐realistic neonicotinoid exposure has sub‐lethal effects on non‐Apis bees: A meta‐analysis49
The relative importance of plasticity versus genetic differentiation in explaining between population differences; a meta‐analysis48
Quantifying impacts of plastic debris on marine wildlife identifies ecological breakpoints48
Habitat amount and distribution modify community dynamics under climate change48
Grazing‐induced biodiversity loss impairs grassland ecosystem stability at multiple scales47
Latitudinal gradient in the intensity of biotic interactions in terrestrial ecosystems: Sources of variation and differences from the diversity gradient revealed by meta‐analysis47
Towards revealing the global diversity and community assembly of soil eukaryotes47
The geography of metapopulation synchrony in dendritic river networks47
Trade‐off between seed dispersal in space and time47
Assessing metacommunity processes through signatures in spatiotemporal turnover of community composition45
Historical decrease in agricultural landscape diversity is associated with shifts in bumble bee species occurrence43
Using a newly introduced framework to measure ecological stressor interactions43
Climate change transforms the functional identity of Mediterranean coralligenous assemblages43
Plant and soil biodiversity have non‐substitutable stabilising effects on biomass production43
Insect and plant invasions follow two waves of globalisation43
Mechanisms underlying host persistence following amphibian disease emergence determine appropriate management strategies43
Interaction diversity explains the maintenance of phytochemical diversity42
Bugs scaring bugs: enemy‐risk effects in biological control systems41
Phenological asynchrony: a ticking time‐bomb for seemingly stable populations?41
Functional traits explain the consistent resistance of biodiversity to plant invasion under nitrogen enrichment41
Structural forecasting of species persistence under changing environments41
Leaf size of woody dicots predicts ecosystem primary productivity41
Developmental plasticity in thermal tolerance: Ontogenetic variation, persistence, and future directions41
Experimental nitrogen fertilisation globally accelerates, then slows decomposition of leaf litter41
Soil fungal mycelia have unexpectedly flexible stoichiometric C:N and C:P ratios41
Directional turnover towards larger‐ranged plants over time and across habitats39
Pesticides do not significantly reduce arthropod pest densities in the presence of natural enemies39
Universal rules of life: metabolic rates, biological times and the equal fitness paradigm39
Diversity and coexistence are influenced by time‐dependent species interactions in a predator–prey system39
Diverging functional strategies but high sensitivity to an extreme drought in tropical dry forests38
Fire frequency, state change and hysteresis in tallgrass prairie38
Why disease ecology needs life‐history theory: a host perspective37
How long do population level field experiments need to be? Utilising data from the 40‐year‐old LTER network37
Drivers of local extinction risk in alpine plants under warming climate37
Measuring habitat complexity and spatial heterogeneity in ecology36
Multiple spatial behaviours govern social network positions in a wild ungulate36
Ecophylogenetics redux36
A place to land: spatiotemporal drivers of stopover habitat use by migrating birds36
Combining range and phenology shifts offers a winning strategy for boreal Lepidoptera35
Hot droughts compromise interannual survival across all group sizes in a cooperatively breeding bird35
Microbe‐mediated adaptation in plants34
Trophic control changes with season and nutrient loading in lakes33
Thermal performance under constant temperatures can accurately predict insect development times across naturally variable microclimates33
Tractable models of ecological assembly32
The allometry of plant height explains species loss under nitrogen addition32
Hydraulic prediction of drought‐induced plant dieback and top‐kill depends on leaf habit and growth form32
Plant volatiles induced by herbivore eggs prime defences and mediate shifts in the reproductive strategy of receiving plants32
General statistical scaling laws for stability in ecological systems31
Ecological and conceptual consequences of Arctic pollution31
Flowering synchrony drives reproductive success in a wind‐pollinated tree31
Landscape‐scale habitat fragmentation is positively related to biodiversity, despite patch‐scale ecosystem decay31
Decay by ectomycorrhizal fungi couples soil organic matter to nitrogen availability31
Making sense of virus size and the tradeoffs shaping viral fitness31
Persistent soil seed banks promote naturalisation and invasiveness in flowering plants31
Advancing nature‐based approaches to address the biodiversity and climate emergency31
A shift from phenol to silica‐based leaf defences during long‐term soil and ecosystem development30
Geographic mosaic of selection by avian predators on hindwing warning colour in a polymorphic aposematic moth30
Assessing the risk of human‐to‐wildlife pathogen transmission for conservation and public health30
On the sensitivity of food webs to multiple stressors30
The hidden ageing costs of sperm competition30
Implications of scale dependence for cross‐study syntheses of biodiversity differences29
Nonlinear responses of ecosystem carbon fluxes to nitrogen deposition in an old‐growth boreal forest29
Leaf trait network architecture shifts with species‐richness and climate across forests at continental scale29
Grassland ecosystem recovery after soil disturbance depends on nutrient supply rate29
Integrating data mining and transmission theory in the ecology of infectious diseases29
Experimental (co)evolution in a multi‐species microbial community results in local maladaptation29
Interactive effects of multiple stressors vary with consumer interactions, stressor dynamics and magnitude29
Reconstructing large interaction networks from empirical time series data29
Landscape modification and nutrient‐driven instability at a distance29
The deep sea is a hot spot of fish body shape evolution29
Impacts of invasive plants on animal behaviour29
Silver‐spoon upbringing improves early‐life fitness but promotes reproductive ageing in a wild bird29
Pesticide resistance in arthropods: Ecology matters too28
Soil properties as key predictors of global grassland production: Have we overlooked micronutrients?28
Predicting how climate change threatens the prey base of Arctic marine predators28
The influence of vector‐borne disease on human history: socio‐ecological mechanisms28
Determinants of community compositional change are equally affected by global change27
A meta‐analysis of global avian survival across species and latitude27
Bryophyte C:N:P stoichiometry, biogeochemical niches and elementome plasticity driven by environment and coexistence27
Systematic bias in studies of consumer functional responses27
Predictive models aren't for causal inference27
Was the COVID‐19 pandemic avoidable? A call for a “solution‐oriented” approach in pathogen evolutionary ecology to prevent future outbreaks27
Global impacts of climate change on avian functional diversity26
Terrestrial ecosystem restoration increases biodiversity and reduces its variability, but not to reference levels: A global meta‐analysis26
Climate change impacts on seabirds and marine mammals: The importance of study duration, thermal tolerance and generation time26
Macrogenetic studies must not ignore limitations of genetic markers and scale26
A broadscale analysis of host‐symbiont cophylogeny reveals the drivers of phylogenetic congruence26
Efficient movement strategies mitigate the energetic cost of dispersal26
How community adaptation affects biodiversity–ecosystem functioning relationships25
Rapid adaptive evolution to drought in a subset of plant traits in a large‐scale climate change experiment25
Local canopy disturbance as an explanation for long‐term increases in liana abundance25
Towards a more precise – and accurate – view of eco‐evolution25
Plant community impact on productivity: Trait diversity or key(stone) species effects?25
Direct and indirect disturbance impacts in forests24
Herbivory meets fungivory: insect herbivores feed on plant pathogenic fungi for their own benefit24
A case for associational resistance: Apparent support for the stress gradient hypothesis varies with study system24
Process‐explicit models reveal pathway to extinction for woolly mammoth using pattern‐oriented validation24
Cooperative breeding and the emergence of multilevel societies in birds24
Biodiversity and yield trade‐offs for organic farming24
Three questions about the eco‐physiology of overwintering underground24
Effects of multiple stressors on the dimensionality of ecological stability24
Enhanced light interception and light use efficiency explain overyielding in young tree communities24
Coexistence barriers confine the poleward range of a globally distributed plant23
Sampling bias exaggerates a textbook example of a trophic cascade23
Dispersers and environment drive global variation in fruit colour syndromes23
Shifting limitation of primary production: experimental support for a new model in lake ecosystems23
A plant–pollinator metanetwork along a habitat fragmentation gradient22
Untangling the complexity of priority effects in multispecies communities22
A general theory of avian migratory connectivity22
Global distribution and evolutionary transitions of angiosperm sexual systems22
Global plant‐frugivore trait matching is shaped by climate and biogeographic history22
Temporal turnover of the soil microbiome composition is guild‐specific22
Systematic variation in the temperature dependence of bacterial carbon use efficiency22
An individual‐based model for the eco‐evolutionary emergence of bipartite interaction networks22
The origins of global biodiversity on land, sea and freshwater22
Ecology and evolutionary biology must elevate BIPOC scholars22
Forest fire induces short‐term shifts in soil food webs with consequences for carbon cycling22
Local stressors mask the effects of warming in freshwater ecosystems22
Global biogeographic patterns of avian morphological diversity22
The ecological causes and consequences of hard and soft selection22
Can I afford to publish? A dilemma for African scholars21
Species interactions have predictable impacts on diversification21
Uncovering patterns of freshwater positive interactions using meta‐analysis: Identifying the roles of common participants, invasive species and environmental context21
Detecting and interpreting higher‐order interactions in ecological communities21
Microbiome influence on host community dynamics: Conceptual integration of microbiome feedback with classical host–microbe theory21
Towards robust statistical inference for complex computer models21
Biota‐mediated carbon cycling—A synthesis of biotic‐interaction controls on blue carbon21
Unveiling ecological assembly rules from commonalities in trait distributions21
Species–habitat networks elucidate landscape effects on habitat specialisation of natural enemies and pollinators21
Phenotypic plasticity masks range‐wide genetic differentiation for vegetative but not reproductive traits in a short‐lived plant21
Stress causes interspecific facilitation within a compost community21
Artificial selection of stable rhizosphere microbiota leads to heritable plant phenotype changes20
Trait dimensions in bacteria and archaea compared to vascular plants20
Meta‐population structure and the evolutionary transition to multicellularity20
Climate‐driven, but dynamic and complex? A reconciliation of competing hypotheses for species’ distributions20
The latitudinal gradient in plant community assembly processes: A meta‐analysis20
Understanding the relationship between dispersal and range size20
Is habitat selection in the wild shaped by individual‐level cognitive biases in orientation strategy?20
Ecology and evolution of cycad‐feeding Lepidoptera20
Offspring polymorphism and bet hedging: a large‐scale, phylogenetic analysis20
Life history mediates the trade‐offs among different components of demographic resilience20
Industrial rearing of edible insects could be a major source of new biological invasions20
Siderophores drive invasion dynamics in bacterial communities through their dual role as public good versus public bad20
Light availability and light demand of plants shape the arbuscular mycorrhizal fungal communities in their roots19
How disturbance history alters invasion success: biotic legacies and regime change19
Behavioural heat‐stress compensation in a cold‐adapted ungulate: Forage‐mediated responses to warming Alpine summers19
Environmental and anthropogenic constraints on animal space use drive extinction risk worldwide19
Specific sequence of arrival promotes coexistence via spatial niche pre‐emption by the weak competitor19
No complementarity no gain—Net diversity effects on tree productivity occur once complementarity emerges during early stand development19
The functional roles of species in metacommunities, as revealed by metanetwork analyses of bird–plant frugivory networks19
Defining an epidemiological landscape that connects movement ecology to pathogen transmission and pace‐of‐life19
Nitrogen enrichment alters multiple dimensions of grassland functional stability via changing compositional stability19
Quantifying the relative importance of variation in predation and the environment for species coexistence19
Species richness and food‐web structure jointly drive community biomass and its temporal stability in fish communities19
Reducing dispersal limitation via seed addition increases species richness but not above‐ground biomass19
The effect of insect food availability on songbird reproductive success and chick body condition: Evidence from a systematic review and meta‐analysis19
Phosphorus supply shifts the quotas of multiple elements in algae and Daphnia: ionomic basis of stoichiometric constraints19
Body size and digestive system shape resource selection by ungulates: A cross‐taxa test of the forage maturation hypothesis19
Disease hotspots or hot species? Infection dynamics in multi‐host metacommunities controlled by species identity, not source location18
Demographic consequences of foraging ecology explain genetic diversification in Neotropical bird species18
Soils and topography control natural disturbance rates and thereby forest structure in a lowland tropical landscape18
Climatic and evolutionary contexts are required to infer plant life history strategies from functional traits at a global scale18
Globally consistent reef size spectra integrating fishes and invertebrates18
Cascading effects of a disease outbreak in a remote protected area18
Ecological conditions predict the intensity of Hendra virus excretion over space and time from bat reservoir hosts18
Changes in flight period predict trends in abundance of Massachusetts butterflies18
Sex roles in birds: Phylogenetic analyses of the influence of climate, life histories and social environment18
Acoustic restoration: Using soundscapes to benchmark and fast‐track recovery of ecological communities18
Soil element coupling is driven by ecological context and atomic mass18
Climate warming can reduce biocontrol efficacy and promote plant invasion due to both genetic and transient metabolomic changes18
Hidden layers of density dependence in consumer feeding rates18
Diversity and extinction risk are inversely related at a global scale17
Are networks of trophic interactions sufficient for understanding the dynamics of multi‐trophic communities? Analysis of a tri‐trophic insect food‐web time‐series17
Residence time determines invasiveness and performance of garlic mustard (Alliaria petiolata) in North America17
The better, the choosier: A meta‐analysis on interindividual variation of male mate choice17
Phylogenetic and functional clustering illustrate the roles of adaptive radiation and dispersal filtering in jointly shaping late‐Quaternary mammal assemblages on oceanic islands17
Net plant interactions are highly variable and weakly dependent on climate at the global scale17
Nutrient identity modifies the destabilising effects of eutrophication in grasslands17
Addressing the Eltonian shortfall with trait‐based interaction models17
Detecting patterns of vertebrate biodiversity across the multidimensional urban landscape17
Technical Comment on Pande et al. (2020): Why invasion analysis is important for understanding coexistence17
A global meta‐analysis reveals higher variation in breeding phenology in urban birds than in their non‐urban neighbours17
Top predators as biodiversity indicators: A meta‐analysis17
Phylogenetic reconstruction of ancestral ecological networks through time for pierid butterflies and their host plants17
The hidden role of multi‐trophic interactions in driving diversity–productivity relationships16
Disentangling key species interactions in diverse and heterogeneous communities: A Bayesian sparse modelling approach16
Global patterns of resilience decline in vertebrate populations16
Combining multiple tactics over time for cost‐effective eradication of invading insect populations16
Disturbance structures canopy and understory productivity along an environmental gradient16
Intensive human land uses negatively affect vertebrate functional diversity16
Revisiting the growth rate hypothesis: Towards a holistic stoichiometric understanding of growth16
Integrating eco‐evolutionary dynamics and modern coexistence theory16
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