Science Enabled

Bontrager, M., Usui, T., Lee‐Yaw, J. A., Anstett, D. N., Branch, H. A., Hargreaves, A. L., … Angert, A. L. (2021). Adaptation across geographic ranges is consistent with strong selection in marginal climates and legacies of range expansion. Evolution. doi:10.1111/evo.14231 https://doi.org/10.1111/evo.14231

Every species experiences limits to its geographic distribution. Some evolutionary models predict that populations at range edges are less well‐adapted to their local environments due to drift, expansion load, or swamping gene flow from the range interior. Alternatively, populations near range edges…

Allstädt, F. J., Koutsodendris, A., Appel, E., Rösler, W., Reichgelt, T., Kaboth-Bahr, S., … Pross, J. (2021). Late Pliocene to early Pleistocene climate dynamics in western North America based on a new pollen record from paleo-Lake Idaho. Palaeobiodiversity and Palaeoenvironments. doi:10.1007/s12549-020-00460-1 https://doi.org/10.1007/s12549-020-00460-1

Marked by the expansion of ice sheets in the high latitudes, the intensification of Northern Hemisphere glaciation across the Plio/Pleistocene transition at ~ 2.7 Ma represents a critical interval of late Neogene climate evolution. To date, the characteristics of climate change in North America duri…

Bazzicalupo, A. L., Whitton, J., & Berbee, M. L. (2019). Over the hills, but how far away? Estimates of mushroom geographic range extents. Journal of Biogeography. doi:10.1111/jbi.13617 https://doi.org/10.1111/jbi.13617

Aim: Geographic distributions of mushroom species remain poorly understood despite their importance for advancing our understanding of the habitat requirements, species interactions and ecosystem functions of this key group of organisms. Here, we estimate geographic range extents (maximum within‐spe…

Mienna, I. M., Speed, J. D. M., Bendiksby, M., Thornhill, A. H., Mishler, B. D., & Martin, M. D. (2019). Differential patterns of floristic phylogenetic diversity across a post‐glacial landscape. Journal of Biogeography. doi:10.1111/jbi.13789 https://doi.org/10.1111/jbi.13789

Aim: In this study, we explored spatial patterns of phylogenetic diversity (PD) and endemism in the flora of Norway and tested hypothesized post‐glacial environmental drivers of PD, including temperature, precipitation, edaphic factors and time since glacial retreat. Location: Norway. Taxon: Vascula…

Chardon, N. I., Pironon, S., Peterson, M. L., & Doak, D. F. (2019). Incorporating intraspecific variation into species distribution models improves distribution predictions, but cannot predict species traits for a wide‐spread plant species. Ecography. doi:10.1111/ecog.04630 https://doi.org/10.1111/ecog.04630

The most common approach to predicting how species ranges and ecological functions will shift with climate change is to construct correlative species distribution models (SDMs). These models use a species’ climatic distribution to determine currently suitable areas for the species and project its po…

Rotllan-Puig, X., & Traveset, A. (2019). Determining the Minimal Background Area for Species Distribution Models: MinBAR Package. doi:10.1101/571182 https://doi.org/10.1101/571182

One of the crucial choices when modelling species distributions using pseudo-absences approaches is the delineation of the background area to fit the model. We hypothesise that there is a minimum background area around the centre of the species distribution that characterizes well enough the range o…

Karger, D. N., Kessler, M., Conrad, O., Weigelt, P., Kreft, H., König, C., & Zimmermann, N. E. (2019). Why tree lines are lower on islands-Climatic and biogeographic effects hold the answer. Global Ecology and Biogeography. doi:10.1111/geb.12897 https://doi.org/10.1111/geb.12897

Aim: To determine the global position of tree line isotherms, compare it with observed local tree limits on islands and mainlands, and disentangle the potential drivers of a difference between tree line and local tree limit. Location: Global. Time period: 1979–2013. Major taxa studied: Trees. Method…