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Bontrager, M., T. Usui, J. A. Lee‐Yaw, D. N. Anstett, H. A. Branch, A. L. Hargreaves, C. D. Muir, and A. L. Angert. 2021. Adaptation across geographic ranges is consistent with strong selection in marginal climates and legacies of range expansion. Evolution 75: 1316–1333. 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., A. Koutsodendris, E. Appel, W. Rösler, T. Reichgelt, S. Kaboth-Bahr, A. A. Prokopenko, and J. Pross. 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 101: 177–195. 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…

Lake, T. A., R. D. Briscoe Runquist, and D. A. Moeller. 2020. Predicting range expansion of invasive species: Pitfalls and best practices for obtaining biologically realistic projections C. Bellard [ed.],. Diversity and Distributions 26: 1767–1779. 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…

de Jesús Hernández-Hernández, M., J. A. Cruz, and C. Castañeda-Posadas. 2020. Paleoclimatic and vegetation reconstruction of the miocene southern Mexico using fossil flowers. Journal of South American Earth Sciences 104: 102827. https://doi.org/10.1016/j.jsames.2020.102827

Concern about the course of the current environmental problems has raised interest in investigating the different scenarios that have taken place in our planet throughout time. To that end, different methodologies have been employed in order to determine the different variables that compose the envi…

Lindberg, C. L., H. M. Hanslin, M. Schubert, T. Marcussen, B. Trevaskis, J. C. Preston, and S. Fjellheim. 2020. Increased above‐ground resource allocation is a likely precursor for independent evolutionary origins of annuality in the Pooideae grass subfamily. New Phytologist 228: 318–329. https://doi.org/10.1111/nph.16666

Semelparous annual plants flower a single time during their one‐year life cycle, investing much of their energy into rapid reproduction. In contrast, iteroparous perennial plants flower multiple times over several years, and partition their resources between reproduction and persistence. To which ex…

van Treuren, R., R. Hoekstra, R. Wehrens, and T. van Hintum. 2020. Effects of climate change on the distribution of crop wild relatives in the Netherlands in relation to conservation status and ecotope variation. Global Ecology and Conservation 23: e01054. https://doi.org/10.1016/j.gecco.2020.e01054

Crop wild relatives (CWR) are wild plant taxa that are genetically related to a cultivated species and are considered rich sources of useful traits for crop improvement. CWR are generally underrepresented in genebanks, while their survival in nature is not guaranteed. Inventories and risk analyses a…

Goodwin, Z. A., P. Muñoz-Rodríguez, D. J. Harris, T. Wells, J. R. I. Wood, D. Filer, and R. W. Scotland. 2020. How long does it take to discover a species? Systematics and Biodiversity 18: 784–793. 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 …

Li, M., J. He, Z. Zhao, R. Lyu, M. Yao, J. Cheng, and L. Xie. 2020. Predictive modelling of the distribution of Clematis sect. Fruticella s. str. under climate change reveals a range expansion during the Last Glacial Maximum. PeerJ 8: e8729. https://doi.org/10.7717/peerj.8729

Background The knowledge of distributional dynamics of living organisms is a prerequisite for protecting biodiversity and for the sustainable use of biotic resources. Clematis sect. Fruticella s. str. is a small group of shrubby, yellow-flowered species distributed mainly in arid and semi-arid areas…

Ringelberg, J. J., N. E. Zimmermann, A. Weeks, M. Lavin, and C. E. Hughes. 2020. Biomes as evolutionary arenas: Convergence and conservatism in the trans‐continental succulent biome A. Moles [ed.],. Global Ecology and Biogeography 29: 1100–1113. https://doi.org/10.1111/geb.13089

Aim: Historically, biomes have been defined based on their structurally and functionally similar vegetation, but there is debate about whether these similarities are superficial, and about how biomes are defined and mapped. We propose that combined assessment of evolutionary convergence of plant fun…

Schubert, M., T. Marcussen, A. S. Meseguer, and S. Fjellheim. 2019. The grass subfamily Pooideae: Cretaceous–Palaeocene origin and climate‐driven Cenozoic diversification G. Jordan [ed.],. Global Ecology and Biogeography. https://doi.org/10.1111/geb.12923

Aim: Frost is among the most dramatic stresses a plant can experience, and complex physiological adaptations are needed to endure long periods of sub‐zero temperatures. Owing to the need to evolve these complex adaptations, transitioning from tropical to temperate climates is regarded as difficult. …