Science Enabled by Specimen Data

Rozefelds, A. C., Stull, G., Hayes, P., & Greenwood, D. R. (2020). The fossil record of Icacinaceae in Australia supports long-standing Palaeo-Antarctic rainforest connections in southern high latitudes. Historical Biology, 1–11. doi:10.1080/08912963.2020.1832089 https://doi.org/10.1080/08912963.2020.1832089

Fossil fruits of Icacinaceae are recorded from two Cenozoic sites in Australia, at Launceston in northern Tasmania and the Poole Creek palaeochannel in northern South Australia, representing the first report of fossil Icacinaceae from Australia. The Launceston material includes two endocarps with br…

Brandt, A. J., Bellingham, P. J., Duncan, R. P., Etherington, T. R., Fridley, J. D., Howell, C. J., … Peltzer, D. A. (2020). Naturalised plants transform the composition and function of the New Zealand flora. Biological Invasions. doi:10.1007/s10530-020-02393-4 https://doi.org/10.1007/s10530-020-02393-4

The New Zealand flora has a high proportion of endemic species but has been invaded by almost the same number of non-native plant species. To support management of invasive plant species, we provide an updated inventory of New Zealand’s naturalised flora and compare it with the native flora to ident…

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

JARAMILLO-VIVANCO, T. S., & BALSLEV, H. (2020). <p><strong>Revision of <em>Otoba</em> (Myristicaceae)</strong></p>. Phytotaxa, 441(2), 143–175. doi:10.11646/phytotaxa.441.2.3 https://doi.org/10.11646/phytotaxa.441.2.3

Otoba is one of six American genera of Myristicaceae and recognized by having three stamens with almost fused to free filaments, globose arillate seeds and absence of bracteoles in the male flower. Species of Otoba are distinguished by a suite of characters, mainly pubescence of the ovary and anther…

Reginato, M., Vasconcelos, T. N. C., Kriebel, R., & Simões, A. O. (2020). Is dispersal mode a driver of diversification and geographical distribution in the tropical plant family Melastomataceae? Molecular Phylogenetics and Evolution, 148, 106815. doi:10.1016/j.ympev.2020.106815 https://doi.org/10.1016/j.ympev.2020.106815

Species of plants with different life history strategies may differ in their seed dispersal mechanisms, impacting their distribution and diversification patterns. Shorter or longer distance dispersal is favored by different dispersal modes, facilitating (or constraining) population isolation, which …

Stropp, J., Umbelino, B., Correia, R. A., Campos-Silva, J. V., Ladle, R. J., & Malhado, A. C. M. (2020). The ghosts of forests past and future: deforestation and botanical sampling in the Brazilian Amazon. Ecography. doi:10.1111/ecog.05026 https://doi.org/10.1111/ecog.05026

The remarkable biodiversity of the Brazilian Amazon is poorly documented and threatened by deforestation. When undocumented areas become deforested, in addition to losing the fauna and flora, we lose the opportunity to know which unique species had occupied a habitat. Here we quantify such knowledge…

Ritter, C. D., Faurby, S., Bennett, D. J., Naka, L. N., ter Steege, H., Zizka, A., … Antonelli, A. (2019). The pitfalls of biodiversity proxies: Differences in richness patterns of birds, trees and understudied diversity across Amazonia. Scientific Reports, 9(1). doi:10.1038/s41598-019-55490-3 https://doi.org/10.1038/s41598-019-55490-3

Most knowledge on biodiversity derives from the study of charismatic macro-organisms, such as birds and trees. However, the diversity of micro-organisms constitutes the majority of all life forms on Earth. Here, we ask if the patterns of richness inferred for macro-organisms are similar for micro-or…

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…

Peterson, A. T., Asase, A., Canhos, D., de Souza, S., & Wieczorek, J. (2018). Data Leakage and Loss in Biodiversity Informatics. Biodiversity Data Journal, 6. doi:10.3897/bdj.6.e26826 https://doi.org/10.3897/bdj.6.e26826

The field of biodiversity informatics is in a massive, “grow-out” phase of creating and enabling large-scale biodiversity data resources. Because perhaps 90% of existing biodiversity data nonetheless remains unavailable for science and policy applications, the question arises as to how these existin…

Crespo-Mendes, N., Laurent, A., & Hauschild, M. Z. (2018). Effect factors of terrestrial acidification in Brazil for use in Life Cycle Impact Assessment. The International Journal of Life Cycle Assessment. doi:10.1007/s11367-018-1560-7 https://doi.org/10.1007/s11367-018-1560-7

Purpose:In Life Cycle Impact Assessment, atmospheric fate factors, soil exposure factors, and effect factors are combined to characterize potential impacts of acidifying substances in terrestrial environments. Due to the low availability of global data sets, effect factors (EFs) have been reported a…