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Mahalanobis distances for ecological niche modelling and outlier detection: implications of sample size, error, and bias for selecting and parameterising a multivariate location and scatter method. PeerJ 9: e11436.
DOI: 10.7717/peerj.11436
Reduction in the potential distribution of bumble bees (Apidae:Bombus) in Mesoamerica under different climate change scenarios: Conservation implications. Global Change Biology 27: 1772.
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Anthropogenic Pressures Lead to Different Patterns of Niche Contraction and Protected Area Cover in Three Species Procapra Gazelles on Qinghai‐Tibet Plateau and Mongolia. Diversity and Distributions 31: .
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Effects of occurrence data density on conservation prioritization strategies. Biological Conservation 284: 110207.
DOI: 10.1016/j.biocon.2023.110207
Rare edges and abundant cores: range-wide variation in abundance in North American birds. Proceedings of the Royal Society B: Biological Sciences 291: .
DOI: 10.1098/rspb.2023.1760
Identifying priority areas for landscape connectivity for three large carnivores in northwestern Mexico and southwestern United States. Landscape Ecology 36: 877.
DOI: 10.1007/s10980-020-01185-4
Long-term environmental data explain better the abundance of the red octopus (Octopus maya) when testing the niche centroid hypothesis. Journal of Experimental Marine Biology and Ecology 544: 151609.
DOI: 10.1016/j.jembe.2021.151609
Ecological marginalization is widespread and increases extinction risk in mammals. Proceedings of the National Academy of Sciences 120: .
DOI: 10.1073/pnas.2205315120
Using species distribution modeling to generate relative abundance information in socio‐politically unstable territories: Conservation of Felidae in the central‐western region of Mexico. Ecology and Evolution 13: .
DOI: 10.1002/ece3.10534
Multiple Long‐Term, Landscape‐Scale Data Sets Reveal Intraspecific Spatial Variation in Temporal Trends for Bird Species. Ecology Letters 27: .
DOI: 10.1111/ele.14531
Individual fitness is decoupled from coarse‐scale probability of occurrence in North American trees. Ecography 44: 789.
DOI: 10.1111/ecog.05446
Species persistence and climatic stability have shaped plant communities of the Atlantic forest biodiversity hotspot. Plant Ecology & Diversity 17: 85.
DOI: 10.1080/17550874.2024.2396285
Abundant‐core thinking clarifies exceptions to the abundant‐center distribution pattern. Ecography 2023: .
DOI: 10.1111/ecog.06365
Making the most of scarce data: Mapping distribution range and variation in population abundance of a threatened narrow-range endemic plant. Journal for Nature Conservation 57: 125889.
DOI: 10.1016/j.jnc.2020.125889
A grazer's niche edge is associated with increasing diet diversity and poor population performance. Ecology Letters 27: .
DOI: 10.1111/ele.14357
Bees travelling south: Climate‐induced range shifts and suitable habitat losses in south‐eastern neotropics. Journal of Biogeography 51: 2259.
DOI: 10.1111/jbi.14989
Using niche centrality within the scope of the nearly neutral theory of evolution to predict genetic diversity in a tropical conifer species‐pair. Journal of Biogeography 47: 2755.
DOI: 10.1111/jbi.13979
Leaf functional traits and ecological niche of Fagus grandifolia and Oreomunnea mexicana in natural forests and plantings as a proxy of climate change. American Journal of Botany 111: .
DOI: 10.1002/ajb2.16322
Using a robust multi‐settings inference framework on published datasets still reveals limited support for the abundant centre hypothesis: More testing needed on other datasets. Global Ecology and Biogeography 30: 2211.
DOI: 10.1111/geb.13376
Occupancy patterns and upper range limits of lowland Bornean birds along an elevational gradient. Journal of Biogeography 46: 2583.
DOI: 10.1111/jbi.13691
Partial Clonality Expands the Opportunity for Spatial Adaptation. The American Naturalist 202: 681.
DOI: 10.1086/726335