Science Rendue Possible

Vasconcelos, T., Boyko, J. D., & Beaulieu, J. M. (2021). Linking mode of seed dispersal and climatic niche evolution in flowering plants. Journal of Biogeography. doi:10.1111/jbi.14292 https://doi.org/10.1111/jbi.14292

Aim: Due to the sessile nature of flowering plants, movements to new geographical areas occur mainly during seed dispersal. Frugivores tend to be efficient dispersers because animals move within the boundaries of their preferable niches, so seeds are more likely to be transported to environments tha…

Oh, D., Kowalski, K. P., Quach, Q. N., Wijesinghege, C., Tanford, P., Dassanayake, M., & Clay, K. (2021). Novel genome characteristics contribute to the invasiveness of Phragmites australis (common reed). Molecular Ecology. doi:10.1111/mec.16293 https://doi.org/10.1111/mec.16293

The rapid invasion of the non-native Phragmites australis (Poaceae, subfamily Arundinoideae) is a major threat to native wetland ecosystems in North America and elsewhere. We describe the first reference genome for P. australis and compare invasive (ssp. australis) and native (ssp. americanus) genot…

Xue, T., Gadagkar, S. R., Albright, T. P., Yang, X., Li, J., Xia, C., … Yu, S. (2021). Prioritizing conservation of biodiversity in an alpine region: Distribution pattern and conservation status of seed plants in the Qinghai-Tibetan Plateau. Global Ecology and Conservation, 32, e01885. doi:10.1016/j.gecco.2021.e01885 https://doi.org/10.1016/j.gecco.2021.e01885

The Qinghai-Tibetan Plateau (QTP) harbors abundant and diverse plant life owing to its high habitat heterogeneity. However, the distribution pattern of biodiversity hotspots and their conservation status remain unclear. Based on 148,283 high-resolution occurrence coordinates of 13,450 seed plants, w…

Grebennikov, K. (2021). Ecological niche modeling to assessment of potential distribution of Neodiprion abietis (Harris, 1841) (Insecta, Hymenoptera, Diprionidae) in Eurasia. International Journal of Agricultural Sciences and Technology, 1(1), 1–7. doi:10.51483/ijagst.1.1.2021.1-7 https://doi.org/10.51483/ijagst.1.1.2021.1-7

In the article first assesses the potential distribution in Eurasia of Neodiprion abietis (Harris, 1841) first time assessed. The species id a widely distributed in North America fir and spruce defoliator, intercepted in 2016 in the Netherlands. Analysis of the literature data on the known distribut…

Wang, C.-J., & Wan, J.-Z. (2021). Functional trait perspective on suitable habitat distribution of invasive plant species at a global scale. Perspectives in Ecology and Conservation. doi:10.1016/j.pecon.2021.07.002 https://doi.org/10.1016/j.pecon.2021.07.002

Plant invasion has been proved to threaten biodiversity conservation and ecosystem maintenance at a global scale. It is a challenge to project suitable habitat distributions of invasive plant species (IPS) for invasion risk assessment at large spatial scales. Interaction outcomes between native and …

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…

Lake, T. A., Briscoe Runquist, R. D., & Moeller, D. A. (2020). Predicting range expansion of invasive species: Pitfalls and best practices for obtaining biologically realistic projections. Diversity and Distributions, 26(12), 1767–1779. doi:10.1111/ddi.13161 https://doi.org/10.1111/ddi.13161

Aim: Species distribution models (SDMs) are widely used to forecast potential range expansion of invasive species. However, invasive species occurrence datasets often have spatial biases that may violate key SDM assumptions. In this study, we examined alternative methods of spatial bias correction a…

Goodwin, Z. A., Muñoz-Rodríguez, P., Harris, D. J., Wells, T., Wood, J. R. I., Filer, D., & Scotland, R. W. (2020). How long does it take to discover a species? Systematics and Biodiversity, 1–10. doi:10.1080/14772000.2020.1751339 https://doi.org/10.1080/14772000.2020.1751339

The description of a new species is a key step in cataloguing the World’s flora. However, this is only a preliminary stage in a long process of understanding what that species represents. We investigated how long the species discovery process takes by focusing on three key stages: 1, the collection …

Folk, R. A., Stubbs, R. L., Mort, M. E., Cellinese, N., Allen, J. M., Soltis, P. S., … Guralnick, R. P. (2019). Rates of niche and phenotype evolution lag behind diversification in a temperate radiation. Proceedings of the National Academy of Sciences, 116(22), 10874–10882. doi:10.1073/pnas.1817999116 https://doi.org/10.1073/pnas.1817999116

Environmental change can create opportunities for increased rates of lineage diversification, but continued species accumulation has been hypothesized to lead to slowdowns via competitive exclusion and niche partitioning. Such density-dependent models imply tight linkages between diversification and…

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…