| scholarly article | Q13442814 |
| P50 | author | Jose M. Montoya | Q55099889 |
| Alfredo Valido | Q56550513 | ||
| Jens M Olesen | Q59556285 | ||
| Guy Woodward | Q63877373 | ||
| Philip H. Warren | Q104745072 | ||
| P2093 | author name string | Bo Ebenman | |
| Mark Emmerson | |||
| P433 | issue | 7 | |
| P921 | main subject | ecological network | Q5333246 |
| P6104 | maintained by WikiProject | WikiProject Ecology | Q10818384 |
| P1104 | number of pages | 8 | |
| P304 | page(s) | 402-409 | |
| P577 | publication date | 2005-07-01 | |
| P1433 | published in | Trends in Ecology & Evolution | Q15265725 |
| P1476 | title | Body size in ecological networks | |
| P478 | volume | 20 |
| Q35663696 | A Multi Size-Level Assessment of Benthic Marine Communities in a Coastal Environment: Are They Different Sides of the Same Coin? |
| Q98465411 | A Teleost Fish Model to Understand Hormonal Mechanisms of Non-breeding Territorial Behavior |
| Q57019475 | A common framework for identifying linkage rules across different types of interactions |
| Q38367276 | A conceptual framework for studying the strength of plant-animal mutualistic interactions |
| Q57230072 | A dirty job: manure removal by dung beetles in both a cattle ranch and laboratory setting |
| Q92967860 | A functional trait approach to identifying life history patterns in stochastic environments |
| Q51689001 | A general model for food web structure. |
| Q35034654 | A method for detecting positive growth autocorrelation without marking individuals |
| Q94686310 | A new framework for growth curve fitting based on the von Bertalanffy Growth Function |
| Q47203979 | A unifying theory for top-heavy ecosystem structure in the ocean |
| Q28473922 | Aboveground herbivory shapes the biomass distribution and flux of soil invertebrates |
| Q28703605 | Abundance is not enough: the need for multiple lines of evidence in testing for ecological stability in the fossil record |
| Q57066861 | Across ecosystem comparisons of size structure: methods, approaches and prospects |
| Q39660695 | Allometric and temporal scaling of movement characteristics in Galapagos tortoises |
| Q33311695 | Allometric degree distributions facilitate food-web stability |
| Q35183754 | Allometric scaling of indirect effects: body size ratios predict non-consumptive effects in multi-predator systems |
| Q37146787 | An intertidal snail shows a dramatic size increase over the past century |
| Q36153080 | Animal diversity and ecosystem functioning in dynamic food webs. |
| Q56457179 | Antagonistic effects of biological invasion and temperature change on body size of island ectotherms |
| Q60912449 | Applying generalized allometric regressions to predict live body mass of tropical and temperate arthropods |
| Q57048806 | Assessing the functional importance of large-bodied invertebrates in experimental headwater streams |
| Q51523740 | Bigger mothers are better mothers: disentangling size-related prenatal and postnatal maternal effects. |
| Q46277952 | Biodiversity and ecosystem functioning in food webs: the vertical diversity hypothesis. |
| Q60450023 | Body Length Determines the Diet and Niche Specialization of Non-Biting Midge Predator (Tanypodinae) Larvae in Shallow Reservoirs |
| Q51644728 | Body downsizing caused by non-consumptive social stress severely depresses population growth rate. |
| Q64230806 | Body mass as a supertrait linked to abundance and behavioral dominance in hummingbirds: A phylogenetic approach |
| Q56522775 | Body mass estimation for †Cyonasua (Procyonidae, Carnivora) and related taxa based on postcranial skeleton |
| Q51115389 | Body size and mortality rates in coral reef fishes: a three-phase relationship. |
| Q35143065 | Body size as a predictor of species loss effect on ecosystem functioning. |
| Q28710268 | Body size distribution of the dinosaurs |
| Q39101860 | Body size drives allochthony in food webs of tropical rivers |
| Q34611673 | Body size is a significant predictor of congruency in species richness patterns: a meta-analysis of aquatic studies |
| Q28601818 | Body size is negatively correlated with trophic position among cyprinids |
| Q22679622 | Body size of Chrysomelidae (Coleoptera, Insecta) in areas with different levels of conservation in South Brazil |
| Q46241711 | Body size variation in aquatic consumers causes pervasive community effects, independent of mean body size. |
| Q38724807 | Body size-based trophic structure of a deep marine ecosystem |
| Q37655933 | Body size-trophic position relationships among fishes of the lower Mekong basin |
| Q59084880 | Body-size shifts in aquatic and terrestrial urban communities |
| Q34630663 | Cannibalism as an interacting phenotype: precannibalistic aggression is influenced by social partners in the endangered Socorro Isopod (Thermosphaeroma thermophilum). |
| Q55425210 | Capacity to support predators scales with habitat size. |
| Q57245774 | Carcass size shapes the structure and functioning of an African scavenging assemblage |
| Q33447078 | Cascading extinctions and community collapse in model food webs |
| Q90430880 | Caught in the web: Spider web architecture affects prey specialization and spider-prey stoichiometric relationships |
| Q30870299 | Challenges in assessing biological recovery from acidification in Swedish lakes |
| Q95824190 | Changes in stream food-web structure across a gradient of acid mine drainage increases local community stability |
| Q57504952 | Chapter 1 Allometry of Body Size and Abundance in 166 Food Webs |
| Q51151832 | Climate change and body size shift in Mediterranean bivalve assemblages: unexpected role of biological invasions |
| Q28751779 | Climate change and freshwater ecosystems: impacts across multiple levels of organization |
| Q97899803 | Climate change and intensive land use reduce soil animal biomass via dissimilar pathways |
| Q30570463 | Climate change impacts in multispecies systems: drought alters food web size structure in a field experiment |
| Q30570477 | Climate change impacts on body size and food web structure on mountain ecosystems. |
| Q34420500 | Climate change in size-structured ecosystems |
| Q37558023 | Community structure affects trophic ontogeny in a predatory fish |
| Q28710066 | Competition drives clumpy species coexistence in estuarine phytoplankton |
| Q64266798 | Competitive interaction with keystone taxa induced negative priming under biochar amendments |
| Q30815747 | Consequences of biodiversity loss for litter decomposition across biomes |
| Q30445504 | Consequences of stage-structured predators: cannibalism, behavioral effects, and trophic cascades |
| Q47314587 | Consumer-resource body-size relationships in natural food webs |
| Q46456682 | Contacts with large, active individuals intensify the predation risk of small conspecifics. |
| Q52723694 | Convergence of trophic interaction strengths in grassland food webs through metabolic scaling of herbivore biomass. |
| Q90389127 | Cooling requirements fueled the collapse of a desert bird community from climate change |
| Q37882773 | Cross-ecosystem differences in stability and the principle of energy flux |
| Q39311017 | Current limitations of global conservation to protect higher vulnerability and lower resilience fish species. |
| Q55665532 | Decline in top predator body size and changing climate alter trophic structure in an oceanic ecosystem. |
| Q51203881 | Defaunation effects on plant recruitment depend on size matching and size trade-offs in seed-dispersal networks. |
| Q39157949 | Deforestation homogenizes tropical parasitoid-host networks |
| Q37253660 | Demands of eicosapentaenoic acid (EPA) in Daphnia: are they dependent on body size? |
| Q35716578 | Detecting Subtle Shifts in Ecosystem Functioning in a Dynamic Estuarine Environment |
| Q34746857 | Diatoms can be an important exception to temperature-size rules at species and community levels of organization |
| Q30357204 | Diet and condition of mesopredators on coral reefs in relation to shark abundance. |
| Q38209952 | Discontinuities, cross-scale patterns, and the organization of ecosystems. |
| Q35904727 | Disentangling the influences of mean body size and size structure on ecosystem functioning: an example of nutrient recycling by a non-native crayfish |
| Q54537077 | Do Performance-Safety Tradeoffs Cause Hypometric Metabolic Scaling in Animals? |
| Q34071894 | Do food web models reproduce the structure of mutualistic networks? |
| Q90697504 | Do larger individuals cope with resource fluctuations better? An artificial selection approach |
| Q64064840 | Does body size predict the buzz-pollination frequencies used by bees? |
| Q44371335 | Does consumption rate scale superlinearly? |
| Q58383375 | Does selective fishing conserve community biodiversity? Predictions from a length-based multispecies model |
| Q58406554 | Does size matter for dispersal distance? |
| Q51724112 | Driving forces from soil invertebrates to ecosystem functioning: the allometric perspective. |
| Q58721367 | Eat whole and less often: ontogenetic shift reveals size specialization on kelp bass by the California moray eel, Gymnothorax mordax |
| Q92836336 | Eco-hydromorphic Classification for Understanding Stream Macroinvertebrate Biodiversity in Brunei Darussalam, Northern Borneo |
| Q34777854 | Ecological emergence of thermal clines in body size. |
| Q36395146 | Ecological impact of the end-Cretaceous extinction on lamniform sharks. |
| Q36541608 | Ecological networks and their fragility |
| Q28137442 | Ecological networks are more sensitive to plant than to animal extinction under climate change |
| Q64057315 | Ecological traits of the world's primates |
| Q45339704 | Ecological, historical and evolutionary determinants of modularity in weighted seed-dispersal networks |
| Q33321025 | Ecosystem functioning in stream assemblages from different regions: contrasting responses to variation in detritivore richness, evenness and density |
| Q57009106 | Effects of directional environmental change on extinction dynamics in experimental microbial communities are predicted by a simple model |
| Q59219976 | Effects of environmental warming and drought on size-structured soil food webs |
| Q57039802 | Effects of increasing nutrient supply and omnivorous feeding on the size spectrum slope: a size-based nutrient-phytoplankton-zooplankton model |
| Q35073421 | Effects of predator richness on prey suppression: a meta-analysis. |
| Q31103257 | Effects of temperature variability on community structure in a natural microbial food web. |
| Q57863959 | Effects of the early Toarcian Oceanic Anoxic Event on ichthyosaur body size and faunal composition in the Southwest German Basin |
| Q30984813 | Eight decades of sampling reveal a contemporary novel fish assemblage in coastal nursery habitats |
| Q33517948 | Environmental DNA sequencing primers for eutardigrades and bdelloid rotifers |
| Q90713264 | Estimating the size distribution of plastics ingested by animals |
| Q98164985 | Evaluation of Particle Size Distribution Metrics to Estimate the Relative Contributions of Different Size Fractions Based on Measurements in Arctic Waters |
| Q36199149 | Experimental whole-stream warming alters community size structure |
| Q36230037 | Extensions of Island Biogeography Theory predict the scaling of functional trait composition with habitat area and isolation |
| Q91794496 | Farming system shapes traits and composition of spider assemblages in Mediterranean cherry orchards |
| Q58793976 | Flow regulation increases food-chain length through omnivory mechanisms in a Mediterranean river network |
| Q33850224 | Food web complexity and allometric scaling relationships in stream mesocosms: implications for experimentation |
| Q33563975 | Food webs are more than the sum of their tritrophic parts |
| Q44137919 | Foraging and vulnerability traits modify predator-prey body mass allometry: freshwater macroinvertebrates as a case study. |
| Q35604819 | Foraging mode affects the evolution of egg size in generalist predators embedded in complex food webs |
| Q52688498 | Form, function, and fitness: pathways to survival. |
| Q28606891 | Fractal Hypothesis of the Pelagic Microbial Ecosystem-Can Simple Ecological Principles Lead to Self-Similar Complexity in the Pelagic Microbial Food Web? |
| Q36015582 | Frog eat frog: exploring variables influencing anurophagy |
| Q38446089 | From mice to elephants: overturning the 'one size fits all' paradigm in marine plankton food chains |
| Q96135501 | Functional diversity of marine megafauna in the Anthropocene |
| Q58694036 | Genetic basis of thermal plasticity variation in Drosophila melanogaster body size |
| Q34845431 | Genetic variation, predator-prey interactions and food web structure. |
| Q57052130 | Geographic signatures in species turnover: decoupling colonization and extinction across a latitudinal gradient |
| Q28584669 | Geohistorical records indicate no impact of the Deepwater Horizon oil spill on oyster body size |
| Q38893812 | Global patterns in predator-prey size relationships reveal size dependency of trophic transfer efficiency |
| Q34104376 | Global warming and hepatotoxin production by cyanobacteria: what can we learn from experiments? |
| Q51147208 | Go big or … don't? A field-based diet evaluation of freshwater piscivore and prey fish size relationships. |
| Q58406927 | Habitat structure and body size distributions: cross-ecosystem comparison for taxa with determinate and indeterminate growth |
| Q57004334 | Handbook of protocols for standardized measurement of terrestrial invertebrate functional traits |
| Q59224337 | Harvest Pressure and Environmental Carrying Capacity: An Ordinal-Scale Model of Effects on Ungulate Prey |
| Q100503948 | High fidelity defines the temporal consistency of host-parasite interactions in a tropical coastal ecosystem |
| Q57805193 | Hope and caution: rewilding to mitigate the impacts of biological invasions |
| Q92077286 | Horizontal and vertical diversity jointly shape food web stability against small and large perturbations |
| Q36765151 | Including trait-based early warning signals helps predict population collapse. |
| Q30679162 | Increases in disturbance and reductions in habitat size interact to suppress predator body size. |
| Q34626395 | Increasing zooplankton size diversity enhances the strength of top-down control on phytoplankton through diet niche partitioning |
| Q30489565 | Indicator Properties of Baltic Zooplankton for Classification of Environmental Status within Marine Strategy Framework Directive |
| Q35799167 | Indirect Energy Flows in Niche Model Food Webs: Effects of Size and Connectance |
| Q46864373 | Individual and species-specific traits explain niche size and functional role in spiders as generalist predators |
| Q36273994 | Influence of ocean acidification on plankton community structure during a winter-to-summer succession: An imaging approach indicates that copepods can benefit from elevated CO2 via indirect food web effects. |
| Q64119792 | Insights into Body Size Evolution: A Comparative Transcriptome Study on Three Species of Asian Sisoridae Catfish |
| Q90703968 | Insights into the assembly rules of a continent-wide multilayer network |
| Q56972737 | Integrating elements and energy through the metabolic dependencies of gross growth efficiency and the threshold elemental ratio |
| Q37938189 | Integrating food web diversity, structure and stability. |
| Q47329726 | Interactive effects of body-size structure and adaptive foraging on food-web stability |
| Q56330320 | Invader Relative Impact Potential: a new metric to understand and predict the ecological impacts of existing, emerging and future invasive alien species |
| Q57021873 | Is fisheries production within Large Marine Ecosystems determined by bottom-up or top-down forcing? |
| Q57039074 | Keystone species in seed dispersal networks are mainly determined by dietary specialization |
| Q57003908 | Lake Baikal amphipods under climate change: thermal constraints and ecological consequences |
| Q36308702 | Large but uneven reduction in fish size across species in relation to changing sea temperatures. |
| Q88785416 | Legacy effects of developmental stages determine the functional role of predators |
| Q44178094 | Linking secondary structure of individual size distribution with nonlinear size-trophic level relationship in food webs |
| Q51716723 | Little left in the tank: metabolic scaling in marine teleosts and its implications for aerobic scope. |
| Q60507254 | Local adaptation reduces the metabolic cost of environmental warming |
| Q55711746 | Loss of functionally unique species may gradually undermine ecosystems. |
| Q34822893 | Mammal predator and prey species richness are strongly linked at macroscales |
| Q92610304 | Mammalian tolerance to humans is predicted by body mass: evidence from long-term archives |
| Q33579858 | Marine biodiversity, ecosystem functioning, and carbon cycles |
| Q47308775 | Measurement of body size and abundance in tests of macroecological and food web theory |
| Q28676979 | Metabolic rate and body size are linked with perception of temporal information |
| Q58042414 | Modeling foundation species in food webs |
| Q36771859 | Modelling disease spread and control in networks: implications for plant sciences. |
| Q35224223 | Modelling size structured food webs using a modified niche model with two predator traits |
| Q21090569 | Morphometry, bite-force, and paleobiology of the late miocene caiman Purussaurus brasiliensis |
| Q30376170 | Multitrophic diversity effects of network degradation. |
| Q39274402 | Network structural properties mediate the stability of mutualistic communities |
| Q26771568 | Networking Our Way to Better Ecosystem Service Provision |
| Q56001294 | New data on the diversity and abundance of small-bodied ornithopods (Dinosauria, Ornithischia) from the Belly River Group (Campanian) of Alberta |
| Q56376038 | Non-native introductions influence fish body size distributions within a dryland river |
| Q27026921 | Novel communities from climate change |
| Q37359153 | On the balance between niche and neutral processes as drivers of community structure along a successional gradient: insights from alpine and sub-alpine meadow communities |
| Q35994217 | On the context-dependent scaling of consumer feeding rates |
| Q34822843 | Ontogenetic functional diversity: size structure of a keystone predator drives functioning of a complex ecosystem |
| Q28647056 | Open science resources for the discovery and analysis of Tara Oceans data |
| Q45281412 | Optimizing size thresholds in a plant-pollinator interaction web: towards a mechanistic understanding of ecological networks |
| Q39285203 | Origin of compartmentalization in food webs. |
| Q34775508 | Parasites affect food web structure primarily through increased diversity and complexity |
| Q49886477 | Parasitism and the Biodiversity-Functioning Relationship |
| Q100524039 | Particulate organic matter as causative factor to eutrophication of subtropical deep freshwater: Role of typhoon (tropical cyclone) in the nutrient cycling |
| Q37947340 | Patterns and processes in abundance-body size relationships for marine benthic invertebrates |
| Q42671164 | Pellets of proof: First glimpse of the dietary composition of adult odonates as revealed by metabarcoding of feces. |
| Q28602859 | Phylogenetic analyses suggest that diversification and body size evolution are independent in insects |
| Q46856205 | Phylogeny and micro-habitats utilized by lizards determine the composition of their endoparasites in the semiarid Caatinga of Northeast Brazil. |
| Q51561692 | Phylogeny versus body size as determinants of food web structure. |
| Q51729607 | Plankton motility patterns and encounter rates. |
| Q56937631 | Plant diversity induces shifts in the functional structure and diversity across trophic levels |
| Q55029573 | Pollen sleuthing for terrestrial plant surveys: Locating plant populations by exploiting pollen movement. |
| Q48141428 | Potential disruption of seed dispersal in the absence of a native Kauai thrush |
| Q57063452 | Predation and competition effects on the size diversity of aquatic communities |
| Q98613080 | Predation shapes the impact of cancer on population dynamics and the evolution of cancer resistance |
| Q60922358 | Predator size-structure and species identity determine cascading effects in a coastal ecosystem |
| Q92172439 | Predator traits determine food-web architecture across ecosystems |
| Q57517290 | Predator-prey mass ratio revisited: does preference of relative prey body size depend on individual predator size? |
| Q40124509 | Predicting the abundance of European stream macroinvertebrates using biological attributes. |
| Q35891424 | Predicting the consequences of species loss using size-structured biodiversity approaches |
| Q28598234 | Predictors of shell size in long-lived lake gastropods |
| Q89530462 | Prehistoric baseline reveals substantial decline of oyster reef condition in a Gulf of Mexico conservation priority area |
| Q33505397 | Press perturbations and indirect effects in real food webs |
| Q46635536 | Prey size structure diminishes cascading effects by increasing interference competition and predation among prey |
| Q58063123 | Projected climate change and the changing biogeography of coastal Mediterranean fishes |
| Q51234226 | Protection of large predators in a marine reserve alters size-dependent prey mortality |
| Q31032113 | Quantifying heterogeneous responses of fish community size structure using novel combined statistical techniques |
| Q33911228 | Re-structuring of marine communities exposed to environmental change: a global study on the interactive effects of species and functional richness |
| Q39973422 | Reconciling the role of organic matter pathways in aquatic food webs by measuring multiple tracers in individuals |
| Q36314729 | Relationships between abiotic environment, plant functional traits, and animal body size at Mount Kilimanjaro, Tanzania |
| Q36776375 | Relationships between body size and abundance in ecology |
| Q51463771 | Resolving the roles of body size and species identity in driving functional diversity. |
| Q90003035 | Rethinking megafauna |
| Q98225711 | Rethinking trophic niches: Speed and body mass colimit prey space of mammalian predators |
| Q56269697 | Seed dispersal by Galápagos tortoises |
| Q38368952 | Shotgun mitogenomics across body size classes in a local assemblage of tropical Diptera: Phylogeny, species diversity and mitochondrial abundance spectrum. |
| Q37068423 | Simple prediction of interaction strengths in complex food webs. |
| Q92984716 | Size dependency of patch departure behavior: evidence from granivorous rodents |
| Q35689179 | Size matters at deep-sea hydrothermal vents: different diversity and habitat fidelity patterns of meio- and macrofauna |
| Q56363687 | Size matters: predation of fish eggs and larvae by native and invasive amphipods |
| Q46852300 | Size-dependent diffusion promotes the emergence of spatiotemporal patterns. |
| Q47189655 | Size-spectra dynamics from stochastic predation and growth of individuals |
| Q96816050 | Small vertebrates are key elements in the frugivory networks of a hyperdiverse tropical forest |
| Q50349551 | Soil resource supply influences faunal size-specific distributions in natural food webs |
| Q38975568 | Spatial and temporal distribution of gerrid (Heteroptera) and predation on microcrustaceans from a tropical shallow lake |
| Q56764661 | Spatio-temporal segregation and size distribution of fish assemblages as related to non-native species occurrence in the middle rio Doce Valley, MG, Brazil |
| Q90372317 | Species diversity as a surrogate for conservation of phylogenetic and functional diversity in terrestrial vertebrates across the Americas |
| Q33817207 | Species traits and interaction rules shape a species-rich seed-dispersal interaction network. |
| Q39292828 | Species, functional groups, and thresholds in ecological resilience |
| Q28829838 | Structure and inference in annotated networks |
| Q57904401 | Taxonomic versus allometric constraints on non-linear interaction strengths |
| Q31160917 | Temporal dynamics in a pollination network. |
| Q33907085 | Testing effects of consumer richness, evenness and body size on ecosystem functioning. |
| Q36670027 | The "Goldilocks factor" in food webs |
| Q38912135 | The Labile Limits of Forbidden Interactions. |
| Q56947991 | The assessment of a global marine ecosystem model on the basis of emergent properties and ecosystem function: a case study with ERSEM |
| Q57232447 | The birds and the seas: body size reconciles differences in the abundance-occupancy relationship across marine and terrestrial vertebrates |
| Q57068499 | The body-size structure of macrobenthos changes predictably along gradients of hydrodynamic stress and organic enrichment |
| Q57066882 | The consequences of size dependent foraging for food web topology |
| Q34032835 | The ecological and evolutionary implications of merging different types of networks. |
| Q34208030 | The effects of body mass on dung removal efficiency in dung beetles |
| Q26750432 | The effects of climatic fluctuations and extreme events on running water ecosystems |
| Q30934132 | The effects of fire severity on macroinvertebrate detritivores and leaf litter decomposition. |
| Q92647297 | The fiddler crab, Minuca pugnax, follows Bergmann's rule |
| Q28655870 | The impact of 850,000 years of climate changes on the structure and dynamics of mammal food webs |
| Q28584568 | The importance of digitized biocollections as a source of trait data and a new VertNet resource |
| Q31131883 | The influence of variability in species trait data on community-level ecological prediction and inference |
| Q46415257 | The macroecology of marine cleaning mutualisms. |
| Q36128431 | The network organization of protein interactions in the spliceosome is reproduced by the simple rules of food-web models |
| Q39289940 | The probabilistic niche model reveals substantial variation in the niche structure of empirical food webs |
| Q28749869 | The probabilistic niche model reveals the niche structure and role of body size in a complex food web |
| Q37220345 | The role of body mass in diet contiguity and food-web structure |
| Q39618017 | The roles of productivity and ecosystem size in determining food chain length in tropical terrestrial ecosystems |
| Q56520747 | The utility of height for the Ediacaran organisms of Mistaken Point |
| Q51345190 | The vulnerability of species to range expansions by predators can be predicted using historical species associations and body size. |
| Q56925227 | Thermogeographic variation in body size of Carcinus maenas, the European green crab |
| Q55285062 | Time- and depth-wise trophic niche shifts in Antarctic benthos. |
| Q46342412 | Top predators determine how biodiversity is partitioned across time and space |
| Q56817107 | Towards novel approaches to modelling biotic interactions in multispecies assemblages at large spatial extents |
| Q55717382 | Trait-based predictions and responses from laboratory mite populations to harvesting in stochastic environments. |
| Q46849951 | Traits and phylogenetic history contribute to network structure across Canadian plant-pollinator communities |
| Q101051184 | Treeline ecotones shape the distribution of avian species richness and functional diversity in south temperate mountains |
| Q58622169 | Trophic trickles and cascades in a complex food web: impacts of a keystone predator on stream community structure and ecosystem processes |
| Q63952167 | Ubiquitous abundance distribution of non-dominant plankton across the global ocean |
| Q59457924 | Unexpected changes in community size structure in a natural warming experiment |
| Q35209496 | Unifying elemental stoichiometry and metabolic theory in predicting species abundances |
| Q98395249 | Unlocking the potential of historical abundance datasets to study biomass change in flying insects |
| Q36479246 | Using community viability analysis to identify fragile systems and keystone species. |
| Q57257681 | Using sensitivity analysis to identify keystone species and keystone links in size-based food webs |
| Q56565945 | Using stable isotope analyses to determine the ecological effects of non-native fishes |
| Q51565944 | Warming alters community size structure and ecosystem functioning. |
| Q30570473 | Warming and nitrogen affect size structuring and density dependence in a host-parasitoid food web |
| Q59220028 | Warming up the system: higher predator feeding rates but lower energetic efficiencies |
| Q88603255 | What drives interaction strengths in complex food webs? A test with feeding rates of a generalist stream predator |
| Q54555257 | When a beetle is too small to carry phoretic mites? A case of hydrophilid beetles (Coleoptera: Hydrophilidae) and Uropoda orbicularis (Acari: Mesostigmata) |
| Q34592910 | When herbivores eat predators: predatory insects effectively avoid incidental ingestion by mammalian herbivores |
| Q58732021 | Zooming into plant-flower visitor networks: an individual trait-based approach |
| Q57900846 | Zooplankton Are Not Fish: Improving Zooplankton Realism in Size-Spectrum Models Mediates Energy Transfer in Food Webs |
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