Measuring beta diversity for presence–absence data
By Patricia Koleff, Kevin J. Gaston, J. Lennon. 2003
1,877 citations recorded by the source corpus.
Subfields: Ecology, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/d49393566bcf40933a2e86a34d75c120873d9f32
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Ecology
- Hanna Tuomisto
- G. Grenouillet
- A. Baselga
- Wilfried Thuiller
- Julian D. Olden
- Jane Elith
- Pierre Legendre
- J. Heino
In Nature and Landscape Conservation
- Wilfried Thuiller
- Julian D. Olden
- Hanna Tuomisto
- A. Baselga
- Pierre Legendre
- G. Grenouillet
- J. Heino
- J. Soininen
Citations in the corpus
- Distance decay of similarity among European urban floras: the impact of anthropogenic activities on β diversity (2008, methodology): “We estimated the level of compositional similarity between pairs of floras using the β-sim dissimilarity index which has a range from 0 to 1, high similarity to low similarity, respectively (Lennon et al., 2001; Koleff et al., 2003).”
- Patterns of beta diversity in Europe: the role of climate, land cover and distance across scales (2012, methodology): “Therefore, we quantified dissimilarity in species composition (beta diversity) using the bsim index (Koleff et al., 2003), which is expressed as bsim ¼ minðb; cÞ minðb; cÞ þ a ð1Þ where a is the number of species that are shared between two grid cells, b is the number of species that occur in the…”
- Functional homogenization exceeds taxonomic homogenization among European fish assemblages (2014, background): “historically totally distinct (a = 0), dissimilarity was entirely driven by turnover, as all the diversity present in the poorest assemblage was also present in the richest one (Koleff et al., 2003).”
- New similarity indices for the assignment of relevés to the vegetation units of an existing phytosociological classification (2005, methodology): “These qualitative and quantitative indices were originally designed to measure the compositional similarity between two sites (Boyce and Ellison 2001; Koleff et al. 2003).”
- From communities to continents: beta diversity of herbivorous insects (2005, background): “These trends combined should result in an increasing rate of species turnover from high to low latitudes, a pattern indeed confirmed for vertebrates and plants, but no information is available on insects (Koleff et al. 2003b, Rodriguez & Arita 2004).”
- Phylogenetic beta diversity: linking ecological and evolutionary processes across space in time. (2008, background): “Beta diversity (often referred to as turnover) is the change in species composition across geographic space (Whittaker 1960, 1972) and can be calculated many different ways ( Koleff et al. 2003 ).”
- Habitat heterogeneity, species diversity and null models (2005, background): “The Wilson-Shmida index (bT) considers differences only in terms of the presence or absence of species (Wilson and Shmida 1984): bT g(H) l(H) 2a (1) where g(H) is the number of species present in habitat 2 but not in habitat 1, l(H) is the number of species present in habitat 1 but not habitat 2,…”
- Scale dependence in the species-richness-productivity relationship: The role of species turnover (2004, result): “Our results using Jaccard’s dissimilarity index as a measure of species turnover were qualitatively similar to results obtained using an alternate measure of species turnover (bsim) advocated by Koleff et al. (2003).”
- A framework for delineating biogeographical regions based on species distributions (2010, methodology): “Three broad categories of indices can be distinguished (Koleff et al., 2003): indices that focus on richness gradients, on differences in species composition or on both.”