| Q57050636 | A model-based approach to studying changes in compositional heterogeneity |
| Q56773958 | A perfect storm: two ecosystem engineers interact to degrade deciduous forests of New Jersey |
| Q49714406 | A regional assessment of white-tailed deer effects on plant invasion |
| Q56332909 | Biotic homogenization in an increasingly urbanized temperate grassland ecosystem |
| Q56924948 | Biotic homogenization: a new research agenda for conservation biogeography |
| Q51165390 | Broadening the ecological context of ungulate-ecosystem interactions: the importance of space, seasonality, and nitrogen. |
| Q58869723 | Climate envelope, life history traits and the resilience of birds facing global change |
| Q56749752 | Colonization and Effects of Garlic Mustard (Alliaria petiolata), European Buckthorn (Rhamnus cathartica), and Bell's Honeysuckle (Lonicera × bella) on Understory Plants After Five Decades in Southern Wisconsin Forests |
| Q56461211 | Consumers and establishment limitations contribute more than competitive interactions in sustaining dominance of the exotic herb garlic mustard in a Wisconsin, USA forest |
| Q56985673 | Deer density and plant palatability predict shrub cover, richness, diversity and aboriginal food value in a North American archipelago |
| Q40090387 | Deer herbivory alters forest response to canopy decline caused by an exotic insect pest. |
| Q57050710 | Distinguishing between turnover and nestedness in the quantification of biotic homogenization |
| Q35135368 | Disturbance by large herbivores alters the relative importance of the ecological processes that influence the assembly pattern in heterogeneous meta-communities |
| Q91168845 | Does functional homogenization accompany taxonomic homogenization of British birds and how do biotic factors and climate affect these processes? |
| Q40674014 | Drivers of observed biotic homogenization in pine barrens of central Wisconsin |
| Q40325394 | Ecological and evolutionary consequences of biotic homogenization |
| Q28315707 | Ecology and management of white-tailed deer in a changing world |
| Q51185341 | Effects of earthworm invasion on plant species richness in northern hardwood forests. |
| Q30577906 | Elk herbivory alters small mammal assemblages in high-elevation drainages |
| Q30389159 | Emerging ecosystems change the spatial distribution of top carnivores even in poorly populated areas |
| Q56427080 | Evaluating taxonomic homogenization of freshwater fish assemblages in Chile |
| Q44469928 | Evaluation of a regional monitoring program's statistical power to detect temporal trends in forest health indicators |
| Q56696005 | Floristic composition and diversity changes over 60 years in eastern mulga communities of south central Queensland, Australia |
| Q56529845 | Forest plant diversity is threatened by Robinia pseudoacacia (black-locust) invasion |
| Q56439955 | From current distinctiveness to future homogenization of the world's freshwater fish faunas |
| Q58869717 | Functional biotic homogenization of bird communities in disturbed landscapes |
| Q56474032 | Gains in native species promote biotic homogenization over four decades in a human-dominated landscape |
| Q55124185 | Habitat quality is more important than matrix quality for bird communities in protected areas. |
| Q33399203 | Herbivory more limiting than competition on early and established native plants in an invaded meadow |
| Q33268338 | Homogenization dynamics and introduction routes of invasive freshwater fish in the Iberian Peninsula |
| Q34057118 | Homogenization patterns of the world's freshwater fish faunas. |
| Q56359253 | Independent Effects of Invasive Shrubs and Deer Herbivory on Plant Community Dynamics |
| Q34553298 | Invasive plants have scale-dependent effects on diversity by altering species-area relationships |
| Q56745103 | Landscape disturbance causes small-scale functional homogenization, but limited taxonomic homogenization, in plant communities |
| Q31143661 | Large, connected floodplain forests prone to flooding best sustain plant diversity |
| Q35083363 | Limited impacts of extensive human land use on dominance, specialization, and biotic homogenization in boreal plant communities |
| Q56769128 | Linking biotic homogenization to habitat type, invasiveness and growth form of naturalized alien plants in North America |
| Q56451874 | Local increases in diversity accompany community homogenization in floodplain forest understories |
| Q30359777 | Long-Term Effects of White-Tailed Deer Exclusion on the Invasion of Exotic Plants: A Case Study in a Mid-Atlantic Temperate Forest. |
| Q34797204 | Long-term regional shifts in plant community composition are largely explained by local deer impact experiments |
| Q56047471 | Monitoring and evaluating the ecological integrity of forest ecosystems |
| Q83345133 | Nature is changing in more ways than one |
| Q56383779 | New Manual of Vascular Plants of Northeastern United States and Adjacent Canada |
| Q56925002 | On defining and quantifying biotic homogenization |
| Q56745272 | Overabundant suburban deer, invertebrates, and the spread of an invasive exotic plant |
| Q56755139 | Phylogenetic measures of plant communities show long-term change and impacts of fire management in tallgrass prairie remnants |
| Q30318830 | Plant extinctions and introductions lead to phylogenetic and taxonomic homogenization of the European flora |
| Q56417572 | Positive plant and bird diversity response to experimental deer population reduction after decades of uncontrolled browsing |
| Q28647250 | Predicting species' vulnerability in a massively perturbed system: the fishes of Lake Turkana, Kenya |
| Q51110253 | Prediction of extinction in plants: interaction of extrinsic threats and life history traits. |
| Q57899795 | Revealing the regime of shallow coral reefs at patch scale by continuous spatial modeling |
| Q42372691 | Sea level rise may increase extinction risk of a saltmarsh ontogenetic habitat specialist |
| Q35115340 | Spatial patterning and floral synchrony among trillium populations with contrasting histories of herbivory |
| Q56777545 | Spatial scale and evolutionary history determine the degree of taxonomic homogenization across island bird assemblages |
| Q51719768 | Spatial segregation of specialists and generalists in bird communities. |
| Q56566991 | Taxonomic and functional homogenization of an endemic desert fish fauna |
| Q46639948 | Tempering threats to temperate forests |
| Q56925029 | The Human Dimensions of Biotic Homogenization |
| Q35646192 | The colonisation of exotic species does not have to trigger faunal homogenisation: lessons from the assembly patterns of arthropods on oceanic islands. |
| Q39127935 | The impact of Sika deer on vegetation in Japan: setting management priorities on a national scale |
| Q46237966 | The paradox of long-term ungulate impact: increase of plant species richness in a temperate forest. |
| Q56767928 | The role of non-native plants and vertebrates in defining patterns of compositional dissimilarity within and across continents |
| Q56774749 | The varying role of population abundance in structuring indices of biotic homogenization |
| Q31114681 | Tracking lags in historical plant species' shifts in relation to regional climate change |
| Q30845352 | Trait--environment relationships remain strong despite 50 years of trait compositional change in temperate forests |
| Q56774574 | Trait-Based Filtering of the Regional Species Pool to Guide Understory Plant Reintroductions in Midwestern Oak Savannas, U.S.A |
| Q46309074 | Ungulates increase forest plant species richness to the benefit of non-forest specialists. |
| Q56438174 | Urbanization promotes non-native woody species and diverse plant assemblages in the New York metropolitan region |
| Q56511385 | Use of a Native Matrix Species to Facilitate Understory Restoration in an Overbrowsed, Invaded Woodland |
| Q42717087 | White-tailed deer are a biotic filter during community assembly, reducing species and phylogenetic diversity |
| Q56743879 | Widespread plant species: natives versus aliens in our changing world |