scholarly article | Q13442814 |
P50 | author | David Mouillot | Q68686696 |
Norman W. H. Mason | Q88480344 | ||
David R. Bellwood | Q22102363 | ||
Sébastien Villéger | Q56439957 | ||
Nicholas A. J. Graham | Q58149774 | ||
P2860 | cites work | Small clades at the periphery of passerine morphological space | Q81816709 |
Biodiversity loss and its impact on humanity | Q22122163 | ||
Ecomorphological selectivity among marine teleost fishes during the end-Cretaceous extinction | Q24649103 | ||
Graptoloid diversity and disparity became decoupled during the Ordovician mass extinction | Q28731493 | ||
Ecological basis of extinction risk in birds: habitat loss versus human persecution and introduced predators | Q28776619 | ||
Species' traits predict the effects of disturbance and productivity on diversity | Q30840353 | ||
Regional vegetation die-off in response to global-change-type drought | Q31010402 | ||
Reorganization of an arid ecosystem in response to recent climate change | Q33181295 | ||
Functional diversity: back to basics and looking forward | Q33243788 | ||
From plant traits to plant communities: a statistical mechanistic approach to biodiversity | Q33259505 | ||
Low functional diversity and no redundancy in British avian assemblages | Q33294915 | ||
Incorporating plant functional diversity effects in ecosystem service assessments | Q33311452 | ||
New multidimensional functional diversity indices for a multifaceted framework in functional ecology | Q33362955 | ||
Loss of functional diversity under land use intensification across multiple taxa | Q33393377 | ||
The intermediate disturbance hypothesis applies to tropical forests, but disturbance contributes little to tree diversity | Q33453820 | ||
Diversity partitioning of Rao's quadratic entropy | Q33509691 | ||
Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation | Q33718334 | ||
Measuring biodiversity to explain community assembly: a unified approach | Q33771136 | ||
Extinction vulnerability of coral reef fishes. | Q33820170 | ||
Invasive species and habitat degradation in Iberian streams: an analysis of their role in freshwater fish diversity loss | Q33881068 | ||
Recent ecological responses to climate change support predictions of high extinction risk | Q33957519 | ||
Advances, challenges and a developing synthesis of ecological community assembly theory | Q33964792 | ||
Rapid worldwide depletion of predatory fish communities | Q34197133 | ||
The functions of biological diversity in an age of extinction | Q34304781 | ||
Diversity in tropical rain forests and coral reefs | Q34684821 | ||
Future hotspots of terrestrial mammal loss | Q35119385 | ||
Range contraction in large pelagic predators | Q35123054 | ||
Trends in wood density and structure are linked to prevention of xylem implosion by negative pressure. | Q39039559 | ||
Multivariate identification of plant functional response and effect traits in an agricultural landscape | Q42611053 | ||
A trait-based test for habitat filtering: convex hull volume | Q42692777 | ||
Documenting loss of large trophy fish from the Florida Keys with historical photographs | Q44050581 | ||
The multidimensionality of the niche reveals functional diversity changes in benthic marine biotas across geological time | Q45145899 | ||
Interactive and cumulative effects of multiple human stressors in marine systems | Q46123465 | ||
A trait-based approach to community assembly: partitioning of species trait values into within- and among-community components. | Q46934904 | ||
Evidence for a three-way trade-off between nitrogen and phosphorus competitive abilities and cell size in phytoplankton | Q47338413 | ||
Testing the species traits-environment relationships: the fourth-corner problem revisited | Q47647254 | ||
Neutral communities may lead to decreasing diversity-disturbance relationships: insights from a generic simulation model. | Q51599659 | ||
A distance-based framework for measuring functional diversity from multiple traits. | Q51633516 | ||
Equal rates of disturbance cause different patterns of diversity. | Q51664842 | ||
A global overview of drought and heat-induced tree mortality reveals emerging climate change risks for forests | Q55966720 | ||
Small fish, big fish, red fish, blue fish: size-biased extinction risk of the world's freshwater and marine fishes | Q56287438 | ||
Decline in native ladybirds in response to the arrival of Harmonia axyridis: early evidence from England | Q56763651 | ||
Not novel, just better: competition between native and non-native plants in California grasslands that share species traits | Q56767343 | ||
LIFE-HISTORY STRATEGIES PREDICT FISH INVASIONS AND EXTIRPATIONS IN THE COLORADO RIVER BASIN | Q56781657 | ||
Functional trait niches of North American lotic insects: traits-based ecological applications in light of phylogenetic relationships | Q56924977 | ||
Scaling environmental change through the community-level: a trait-based response-and-effect framework for plants | Q57007971 | ||
Factors Preventing the Recovery of New Zealand Forests Following Control of Invasive Deer | Q57009355 | ||
Climatic constraints on trait-based forest assembly | Q57026281 | ||
Let the concept of trait be functional! | Q57051570 | ||
PLANT FUNCTIONAL MARKERS CAPTURE ECOSYSTEM PROPERTIES DURING SECONDARY SUCCESSION | Q57051610 | ||
Predicting changes in community composition and ecosystem functioning from plant traits: revisiting the Holy Grail | Q57051630 | ||
Rao's quadratic entropy as a measure of functional diversity based on multiple traits | Q57069649 | ||
Fire-induced tree mortality in a neotropical forest: the roles of bark traits, tree size, wood density and fire behavior | Q57183057 | ||
The partitioning of diversity: showing Theseus a way out of the labyrinth | Q57195201 | ||
The underpinnings of the relationship of species richness with space and time | Q57198501 | ||
Size structural change in lightly exploited coral reef fish communities: evidence for weak indirect effects | Q57232477 | ||
Predicting trophic guild and diet overlap from functional traits: statistics, opportunities and limitations for marine ecology | Q58063140 | ||
Using life-history traits to explain bird population responses to changing weather variability | Q59048971 | ||
Matching species traits to environmental variables: a new three-table ordination method | Q59049757 | ||
More species, but all do the same: contrasting effects of flood disturbance on ground beetle functional and species diversity | Q59269584 | ||
Disentangling plant trait responses to livestock grazing from spatio-temporal variation: the partial RLQ approach | Q59392459 | ||
Functional versatility supports coral reef biodiversity | Q60451756 | ||
Thresholds and multiple scale interaction of environment, resource use, and market proximity on reef fishery resources in the Solomon Islands | Q60453767 | ||
Functional diversity of herbaceous species under different fire frequencies in Brazilian savannas | Q60473362 | ||
Functional diversity measures: an overview of their redundancy and their ability to discriminate community assembly rules | Q60534574 | ||
Stand development moderates effects of ungulate exclusion on foliar traits in the forests of New Zealand | Q60536526 | ||
Testing the response of macroinvertebrate functional structure and biodiversity to flooding and confinement | Q60557330 | ||
The new diversity: management gains through insights into the functional diversity of communities | Q60571677 | ||
What determines disturbance-productivity-diversity relationships? The effect of scale, species and environment on richness patterns in an Australian woodland | Q61466438 | ||
P433 | issue | 3 | |
P1104 | number of pages | 11 | |
P304 | page(s) | 167-177 | |
P577 | publication date | 2012-11-08 | |
P1433 | published in | Trends in Ecology & Evolution | Q15265725 |
P1476 | title | A functional approach reveals community responses to disturbances | |
P478 | volume | 28 |
Q57069046 | A Catalogue of Marine Biodiversity Indicators |
Q35954710 | A Trait-Based Approach to Advance Coral Reef Science |
Q94601008 | A database of functional traits for spiders from native forests of the Iberian Peninsula and Macaronesia |
Q41550419 | A functional approach to the structural complexity of coral assemblages based on colony morphological features |
Q92491491 | A global database for metacommunity ecology, integrating species, traits, environment and space |
Q55021101 | A global mismatch in the protection of multiple marine biodiversity components and ecosystem services. |
Q56427812 | A plant strategy approach to understand multidecadal change in community assembly processes in Australian grassy woodlands |
Q90273816 | A theory of pulse dynamics and disturbance in ecology |
Q56446924 | A trait-based approach for assessing and mapping niche overlap between native and exotic species: the Mediterranean coastal fish fauna as a case study |
Q35838907 | A trait-based metric sheds new light on the nature of the body size-depth relationship in the deep sea. |
Q35928436 | AM and DSE colonization of invasive plants in urban habitat: a study of Upper Silesia (southern Poland) |
Q60367369 | Accounting for intraspecific diversity when examining relationships between non-native species and functional diversity |
Q55380105 | An automated device for the digitization and 3D modelling of insects, combining extended-depth-of-field and all-side multi-view imaging. |
Q97548621 | Are endemic species necessarily ecological specialists? Functional variability and niche differentiation of two threatened Dianthus species in the montane steppes of northeastern Iran |
Q43969419 | Are functional traits a good predictor of global change impacts on tree species abundance dynamics in a subtropical forest? |
Q35944959 | Assessing the Importance of Intraspecific Variability in Dung Beetle Functional Traits |
Q55436445 | Assessing the multi-scale predictive ability of ecosystem functional attributes for species distribution modelling. |
Q38598746 | Assessing the relationships between phylogenetic and functional singularities in sharks (Chondrichthyes). |
Q35454830 | Association of extinction risk of saproxylic beetles with ecological degradation of forests in Europe. |
Q33948851 | Asynchrony of taxonomic, functional and phylogenetic diversity in birds |
Q93134722 | Avian functional responses to landscape recovery |
Q35940497 | Avian responses to an extreme ice storm are determined by a combination of functional traits, behavioural adaptations and habitat modifications |
Q36054825 | Bat and bird diversity along independent gradients of latitude and tree composition in European forests |
Q36217452 | Bee communities along a prairie restoration chronosequence: similar abundance and diversity, distinct composition. |
Q35799488 | Biodiversity and Resilience of Ecosystem Functions |
Q61454905 | Biogeography of functional trait diversity in the Taiwanese reef fish fauna |
Q35342141 | Biotic homogenization and differentiation of soil faunal communities in the production forest landscape: taxonomic and functional perspectives. |
Q92963458 | Biotic predictors complement models of bat and bird responses to climate and tree diversity in European forests |
Q46748956 | Can species traits predict the susceptibility of riverine fish to water resource development? An Australian case study |
Q60300895 | Change in fish functional diversity and assembly rules in the course of tidal marsh restoration |
Q61797124 | Changes in species richness and composition of boreal waterbird communities: a comparison between two time periods 25 years apart |
Q56433928 | Characteristic and derived diversity: implementing the species pool concept to quantify conservation condition of habitats |
Q63388448 | Chronic fertilization and irrigation gradually and increasingly restructure grassland communities |
Q30801150 | Climate extremes drive changes in functional community structure |
Q51145964 | Comparing functional traits and abundance of invasive versus native woodwasps |
Q64359254 | Comparing species richness, functional diversity and functional composition of waterbird communities along environmental gradients in the neotropics |
Q90783094 | Competition and specialization in an African forest carnivore community |
Q31165064 | Consistent role of Quaternary climate change in shaping current plant functional diversity patterns across European plant orders |
Q30315422 | Contrasting changes in the abundance and diversity of North American bird assemblages from 1971 to 2010. |
Q47176860 | Contrasting responses of functional diversity to major losses in taxonomic diversity |
Q30666633 | Controls on soil microbial community stability under climate change |
Q41074673 | Cost-effective conservation of amphibian ecology and evolution. |
Q58385451 | Cumulative effects of fire and drought in Mediterranean ecosystems |
Q39311017 | Current limitations of global conservation to protect higher vulnerability and lower resilience fish species. |
Q38209952 | Discontinuities, cross-scale patterns, and the organization of ecosystems. |
Q57020293 | Disentangling relationships between plant diversity and decomposition processes under forest restoration |
Q55056301 | Disentangling the pathways of land use impacts on the functional structure of fish assemblages in Amazon streams. |
Q33856725 | Distance-based functional diversity measures and their decomposition: a framework based on Hill numbers |
Q38994995 | Disturbance by an endemic rodent in an arid shrubland is a habitat filter: effects on plant invasion and taxonomical, functional and phylogenetic community structure |
Q36364978 | Disturbance-induced phytoplankton regime shifts and recovery of cyanobacteria dominance in two subtropical reservoirs |
Q35212948 | Does logging and forest conversion to oil palm agriculture alter functional diversity in a biodiversity hotspot? |
Q31031939 | Drought stress limits the geographic ranges of two tree species via different physiological mechanisms |
Q63071685 | Ecological continuity and transformation after the Permo-Triassic mass extinction in northeastern Panthalassa |
Q37296673 | Ecology of Caribbean sponges: are top-down or bottom-up processes more important? |
Q53077453 | Effect of tropical forest disturbance on the competitive interactions within a diverse ant community. |
Q92538396 | Effects of forest management on vertebrates: synthesizing two decades of data from hardwood forests in Missouri, USA |
Q90726500 | Effects of patch size and basal area on avian taxonomic and functional diversity in pine forests: Implication for the influence of habitat quality on the species-area relationship |
Q112669973 | Effects of time since invasion and control actions on a coastal ecosystem invaded by non‐native pine trees |
Q56391660 | Environmental determinants of fish community structure in gravel pit lakes |
Q58537735 | Evidence of neotropical anuran community disruption on rice crops: a multidimensional evaluation |
Q92483303 | Exploitation may influence the climate resilience of fish populations through removing high performance metabolic phenotypes |
Q28657761 | Fifty million years of herbivory on coral reefs: fossils, fish and functional innovations |
Q56380388 | Fish assemblages in Atlantic Forest streams: the relative influence of local and catchment environments on taxonomic and functional species |
Q91272218 | Floodplain land cover affects biomass distribution of fish functional diversity in the Amazon River |
Q57257373 | Forest fragmentation and loss reduce richness, availability, and specialization in tropical hummingbird communities |
Q62928818 | Four decades of functional community change reveals gradual trends and low interlinkage across trophic groups in a large marine ecosystem |
Q61796979 | Frequency of disturbance alters diversity, function, and underlying assembly mechanisms of complex bacterial communities |
Q97519395 | Functional Diversity of Riparian Woody Vegetation Is Less Affected by River Regulation in the Mediterranean Than Boreal Region |
Q59134869 | Functional Redundancy in bird community decreases with riparian forest width reduction |
Q57438285 | Functional Role of the Herbaceous Layer in Eastern Deciduous Forest Ecosystems |
Q59789387 | Functional biodiversity loss along natural CO gradients |
Q57067963 | Functional diversity of North American broad-leaved trees is codetermined by past and current environmental factors |
Q96135501 | Functional diversity of marine megafauna in the Anthropocene |
Q36308622 | Functional diversity response to hardwood forest management varies across taxa and spatial scales |
Q57263465 | Functional ecology of fish: current approaches and future challenges |
Q34281213 | Functional over-redundancy and high functional vulnerability in global fish faunas on tropical reefs. |
Q58841318 | Functional responses of multitaxa communities to disturbance and stress gradients in a restored floodplain |
Q92073328 | Functional shifts in bird communities from semi-natural oak forests to conifer plantations are not consistent across Europe |
Q58087977 | Functional traits reveal early responses in marine reserves following protection from fishing |
Q28601193 | Functional traits, convergent evolution, and periodic tables of niches |
Q36145728 | Functional, size and taxonomic diversity of fish along a depth gradient in the deep sea |
Q57068033 | Geographic patterns in functional diversity deficits are linked to glacial-interglacial climate stability and accessibility |
Q92740671 | Global vulnerability of marine mammals to global warming |
Q56460575 | Going beyond taxonomic diversity: deconstructing biodiversity patterns reveals the true cost of iceplant invasion |
Q90291290 | Habitat effects on intra-species variation in functional morphology: Evidence from freshwater fish |
Q57004334 | Handbook of protocols for standardized measurement of terrestrial invertebrate functional traits |
Q90289058 | Harnessing global fisheries to tackle micronutrient deficiencies |
Q92208601 | Herbivorous fish rise as a destructive fishing practice falls in an Indonesian marine national park |
Q57046262 | Heterogeneous flows foster heterogeneous assemblages: relationships between functional diversity and hydrological heterogeneity in riparian plant communities |
Q98153723 | High environmental stress and productivity increase functional diversity along a deep-sea hydrothermal vent gradient |
Q34784131 | High intraspecific variability in the functional niche of a predator is associated with ontogenetic shift and individual specialization. |
Q49830608 | Homogenization and impoverishment of taxonomic and functional diversity of ants in Eucalyptus plantations |
Q56330476 | Impact of anthropogenic disturbances on a diverse riverine fish assemblage in Fiji predicted by functional traits |
Q39312342 | Improving understanding of the functional diversity of fisheries by exploring the influence of global catch reconstruction |
Q56837340 | Incorporating intraspecific trait variation into functional diversity: Impacts of selective logging on birds in Borneo |
Q36106957 | Indices for assessing coral reef fish biodiversity: the need for a change in habits |
Q35195428 | Inferring resilience to fragmentation-induced changes in plant communities in a semi-arid Mediterranean ecosystem |
Q34373376 | Integrating abundance and functional traits reveals new global hotspots of fish diversity |
Q58643147 | Integrating taxonomic and trait analyses to assess the impact of damming on fish communities in a northern cold region river |
Q34889744 | Interactions in the microbiome: communities of organisms and communities of genes |
Q92646884 | Intercontinental trends in functional and phylogenetic structure of stream fish assemblages |
Q56393654 | Invasion of exotic piscivores causes losses of functional diversity and functionally unique species in Japanese lakes |
Q51731217 | Land use change has stronger effects on functional diversity than taxonomic diversity in tropical Andean hummingbirds. |
Q57004358 | Land-use change promotes avian diversity at the expense of species with unique traits |
Q57201151 | Land-use effects on the functional distinctness of arthropod communities |
Q36258970 | Land-use type and intensity differentially filter traits in above- and below-ground arthropod communities |
Q35814703 | Landscape simplification filters species traits and drives biotic homogenization |
Q64084109 | Large-sized rare tree species contribute disproportionately to functional diversity in resource acquisition in African tropical forest |
Q62084526 | Light limitation increases multidimensional trait evenness in phytoplankton populations |
Q56942336 | Linking functional diversity and ecosystem processes: A framework for using functional diversity metrics to predict the ecosystem impact of functionally unique species |
Q36022914 | Linking multidimensional functional diversity to quantitative methods: a graphical hypothesis--evaluation framework |
Q36014892 | Linking species functional roles to their network roles. |
Q56379345 | Linking the impacts of plant invasion on community functional structure and ecosystem properties |
Q39268073 | Long-term resilience of above- and below ground ecosystem components among contrasting ecosystems |
Q46263019 | Mapping functional diversity from remotely sensed morphological and physiological forest traits. |
Q57901132 | Mare Incognitum: A Glimpse into Future Plankton Diversity and Ecology Research |
Q27342219 | Marine reserves lag behind wilderness in the conservation of key functional roles |
Q57525159 | Modelling climate change impacts on marine fish populations: process-based integration of ocean warming, acidification and other environmental drivers |
Q35836274 | Moderate land use changes plant functional composition without loss of functional diversity in India's Western Ghats |
Q33933170 | New insights into the consequences of post-windthrow salvage logging revealed by functional structure of saproxylic beetles assemblages |
Q35737030 | No evidence for leaf-trait dissimilarity effects on litter decomposition, fungal decomposers, and nutrient dynamics |
Q35995737 | Non-Random Variability in Functional Composition of Coral Reef Fish Communities along an Environmental Gradient |
Q36308697 | On the risks of using dendrograms to measure functional diversity and multidimensional spaces to measure phylogenetic diversity: a comment on Sobral et al. (2016). |
Q57229992 | On the use of predator traits and distribution in environmental impact assessment: the trophic/dispersal sufficiency concept |
Q30839268 | Opportunities and challenges in deriving phytoplankton diversity measures from individual trait-based data obtained by scanning flow-cytometry |
Q51160398 | Optimising Methods for Dung Beetle (Coleoptera: Scarabaeidae) Sampling in Brazilian Pastures. |
Q35987801 | Organic amendments increase phylogenetic diversity of arbuscular mycorrhizal fungi in acid soil contaminated by trace elements |
Q90208324 | Passive rewilding may (also) restore phylogenetically rich and functionally resilient forest plant communities |
Q56755139 | Phylogenetic measures of plant communities show long-term change and impacts of fire management in tallgrass prairie remnants |
Q38808565 | Phylogenetic perspectives on reef fish functional traits |
Q57657845 | Phytoplankton functional response to spatial and temporal differences in a cold and oligotrophic lake |
Q58261126 | Post-Fire Salvage Logging Imposes a New Disturbance that Retards Succession: The Case of Bryophyte Communities in a Macaronesian Laurel Forest |
Q30885396 | Predicting climate-driven regime shifts versus rebound potential in coral reefs |
Q101248836 | Pre‐fire vegetation drives post‐fire outcomes in sagebrush ecosystems: evidence from field and remote sensing data |
Q91496547 | Projected impacts of climate change on functional diversity of frugivorous birds along a tropical elevational gradient |
Q96136277 | Pyrodiversity promotes interaction complementarity and population resistance |
Q57193908 | REVIEW: On the species abundance distribution in applied ecology and biodiversity management |
Q30902767 | Rapid adjustment of bird community compositions to local climatic variations and its functional consequences |
Q91937010 | Rapid redistribution of agricultural land alters avian richness, abundance, and functional diversity |
Q51297232 | Rare species contribute disproportionately to the functional structure of species assemblages. |
Q91974992 | Reduced fish diversity despite increased fish biomass in a Gulf of California Marine Protected Area |
Q36196399 | Regional diversity reverses the negative impacts of an alien predator on local species-poor communities. |
Q98563660 | Reintroduced grazers and prescribed fire effects on beetle assemblage structure and function in restored grasslands |
Q57008189 | Relationships among taxonomic, functional, and phylogenetic ant diversity across the biogeographic regions of Europe |
Q58348409 | Relationships between structural complexity, coral traits, and reef fish assemblages |
Q59138583 | Remotely sensed habitat variables are poor surrogates for functional traits of rocky reef fish assemblages |
Q55019095 | Resource diversity and provenance underpin spatial patterns in functional diversity across native and exotic species. |
Q36319151 | Responses of coral reef fishes to past climate changes are related to life-history traits |
Q89800815 | Retention forestry influences understory diversity and functional identity |
Q57269514 | Richness is not all: how changes in avian functional diversity reflect major landscape modification caused by pine plantations |
Q110697718 | Seasonality in the Brazilian Pantanal influences avian functional diversity |
Q58556303 | Sediment deposition from eroding peatlands alters headwater invertebrate biodiversity |
Q92126947 | Seedling traits predict drought-induced mortality linked to diversity loss |
Q28603297 | Selective logging: does the imprint remain on tree structure and composition after 45 years? |
Q35848545 | Similarity in the difference: changes in community functional features along natural and anthropogenic stress gradients. |
Q96578846 | Singing streams: Describing freshwater soundscapes with the help of acoustic indices |
Q41139961 | Small fire refugia in the grassy matrix and the persistence of Afrotemperate forest in the Drakensberg mountains. |
Q64068872 | Social-ecological alignment and ecological conditions in coral reefs |
Q90098028 | Spatiotemporal effects of logging and fire on tall, wet temperate eucalypt forest birds |
Q56417427 | Species and functional trait turnover in response to broad-scale change and an invasive species |
Q46271301 | Species traits and connectivity constrain stochastic community re-assembly |
Q36319911 | Street trees reduce the negative effects of urbanization on birds. |
Q31104873 | Strong paleoclimatic legacies in current plant functional diversity patterns across Europe |
Q58406891 | Structural complexity mediates functional structure of reef fish assemblages among coral habitats |
Q91886506 | Taxonomic and functional diversity of insect herbivore assemblages associated with the canopy-dominant trees of the Azorean native forest |
Q46302247 | Template for using biological trait groupings when exploring large-scale variation in seafloor multifunctionality. |
Q46237360 | Temporal and spatial differences between taxonomic and trait biodiversity in a large marine ecosystem: Causes and consequences |
Q95641646 | The Influence of Forests on Freshwater Fish in the Tropics: A Systematic Review |
Q55870210 | The Pliocene marine megafauna extinction and its impact on functional diversity |
Q92406836 | The conservation value of cacao agroforestry for bird functional diversity in tropical agricultural landscapes |
Q58208110 | The differential influences of human-induced disturbances on tree regeneration community: a landscape approach |
Q36381287 | The effects of restoring logged tropical forests on avian phylogenetic and functional diversity |
Q63071041 | The evolution of traits and functions in herbivorous coral reef fishes through space and time |
Q37044937 | The impact of individual and combined abiotic factors on daily otolith growth in a coral reef fish |
Q46847976 | The impact of livestock grazing on plant diversity: an analysis across dryland ecosystems and scales in southern Africa |
Q35999123 | The meaning of functional trait composition of food webs for ecosystem functioning. |
Q28607953 | The relationship between pond habitat depth and functional tadpole diversity in an agricultural landscape |
Q56926269 | The shape of success in a turbulent world: wave exposure filtering of coral reef herbivory |
Q99579691 | Toward spatio-temporal delineation of positive interactions in ecology |
Q33807928 | Trait choice profoundly affected the ecological conclusions drawn from functional diversity measures |
Q38754244 | Traits Without Borders: Integrating Functional Diversity Across Scales |
Q101127212 | Tricky partners: native plants show stronger interaction preferences than their exotic counterparts |
Q57135217 | Tropical dung beetle morphological traits predict functional traits and show intraspecific differences across land uses |
Q51244678 | Unexpected high vulnerability of functions in wilderness areas: evidence from coral reef fishes. |
Q40502467 | Urbanization reduces and homogenizes trait diversity in stream macroinvertebrate communities |
Q58648955 | Using a trait-based approach to measure the impact of dam closure in fish communities of a Neotropical River |
Q56331006 | Vegetation dynamics during last 35,000 years at a cold desert locale: preferential loss of forbs with increased aridity |
Q57134713 | Weak functional response to agricultural landscape homogenisation among plants, butterflies and birds |
Q102154112 | What do you mean "functional" in ecology? Patterns versus processes |
Q35653758 | When does diversity matter? Species functional diversity and ecosystem functioning across habitats and seasons in a field experiment |
Q56379538 | Whether disturbances alter salt marsh soil structure dramatically affectsSpartina alterniflorarecolonization rate |
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