Ciência habilitada

Li, X., Li, B., Wang, G., Zhan, X., & Holyoak, M. (2020). Deeply digging the interaction effect in multiple linear regressions using a fractional-power interaction term. MethodsX, 7, 101067. doi:10.1016/j.mex.2020.101067 https://doi.org/10.1016/j.mex.2020.101067

In multiple regression Y ~ β0 + β1X1 + β2X2 + β3X1 X2 + ɛ., the interaction term is quantified as the product of X1 and X2. We developed fractional-power interaction regression (FPIR), using βX1M X2N as the interaction term. The rationale of FPIR is that the slopes of Y-X1 regression along the X2 gr…

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 …

Hochmair, H. H., Scheffrahn, R. H., Basille, M., & Boone, M. (2020). Evaluating the data quality of iNaturalist termite records. PLOS ONE, 15(5), e0226534. doi:10.1371/journal.pone.0226534 https://doi.org/10.1371/journal.pone.0226534

Citizen science (CS) contributes to the knowledge about species distributions, which is a critical foundation in the studies of invasive species, biological conservation, and response to climatic change. In this study, we assessed the value of CS for termites worldwide. First, we compared the abunda…

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…

Schubert, M., Marcussen, T., Meseguer, A. S., & Fjellheim, S. (2019). The grass subfamily Pooideae: Cretaceous–Palaeocene origin and climate‐driven Cenozoic diversification. Global Ecology and Biogeography. doi:10.1111/geb.12923 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. …

Scharff, N., Coddington, J. A., Blackledge, T. A., Agnarsson, I., Framenau, V. W., Szűts, T., … Dimitrov, D. (2019). Phylogeny of the orb‐weaving spider family Araneidae (Araneae: Araneoidea). Cladistics. doi:10.1111/cla.12382 https://doi.org/10.1111/cla.12382

We present a new phylogeny of the spider family Araneidae based on five genes (28S, 18S, COI, H3 and 16S) for 158 taxa, identified and mainly sequenced by us. This includes 25 outgroups and 133 araneid ingroups representing the subfamilies Zygiellinae Simon, 1929, Nephilinae Simon, 1894, and the typ…

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…

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…

Crespo-Mendes, N., Laurent, A., Bruun, H. H., & Hauschild, M. Z. (2019). Relationships between plant species richness and soil pH at the level of biome and ecoregion in Brazil. Ecological Indicators, 98, 266–275. doi:10.1016/j.ecolind.2018.11.004 https://doi.org/10.1016/j.ecolind.2018.11.004

Soil pH has been used to indicate how changes in soil acidity can influence species loss. The correlation between soil pH and plant species richness has mainly been studied in North America and Europe, while there is a lack of studies exploring Tropical floras. Here, our aim was therefore to investi…