Beyond taxonomic diversity patterns: how do α, β and γ components of bird functional and phylogenetic diversity respond to environmental gradients across France?
By C. Meynard, V. Devictor, David Mouillot, Wilfried Thuiller, Frédéric Jiguet, N. Mouquet. 2011
235 citations recorded by the source corpus.
Subfields: Ecological Modeling, Ecology, Evolution, Behavior and Systematics, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/63029bb20c043c629a2fb8ae9be34935d5101edd
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Ecological Modeling
- Frédéric Jiguet
- Wilfried Thuiller
- Francesco de Bello
- V. Devictor
- Pedro Cardoso
- J. Heino
- Romain Julliard
- Denis Couvet
In Ecology, Evolution, Behavior and Systematics
- Francesco de Bello
- Frédéric Jiguet
- Pedro Cardoso
- J. Heino
- David Mouillot
- Wilfried Thuiller
- V. Devictor
- José Carlos Carvalho
In Nature and Landscape Conservation
- Frédéric Jiguet
- Wilfried Thuiller
- Francesco de Bello
- J. Heino
- Pedro Cardoso
- David Mouillot
- V. Devictor
- Dénes Schmera
Citations in the corpus
- Drivers of β‐diversity along latitudinal gradients revisited (2013, background): “The latitudinal diversity gradient – the number of species per unit area decreases from the equator to poles – has been known for over a century (Darwin, 1859; Wallace, 1878), but the causes of this diversity gradient remain poorly resolved (Mittelbach et al., 2007).”
- From diversity indices to community assembly processes: a test with simulated data (2012, background): “This combination favours the coexistence of different but functionally related species in local communities (Mizera and Meszena 2003).”
- Patterns, Causes, and Consequences of Anthropocene Defaunation (2016, background): “As with PD, anthropogenic change generally tends to cause higher FD loss than species loss, and high functional loss may be observed even without loss in α-diversity (D’agata et al. 2014, Meynard et al. 2011).”
- Contrasting changes in taxonomic, phylogenetic and functional diversity during a long‐term succession: insights into assembly processes (2013, background): “Second, phylogenetic diversity may represent a more inclusive overall measure of ecological similarity than measures of functional diversity, which are based on a limited set of traits (Cadotte et al. 2009; Meynard et al. 2011).”
- French citizens monitoring ordinary birds provide tools for conservation and ecological sciences (2012, methodology): “In France, a breeding bird survey is running since 1989 and offers keen birdwatchers to count spring birds annually during 5 min exactly on 10 fix points within a randomly selected square.”
- Partitioning taxon, phylogenetic and functional beta diversity into replacement and richness difference components (2014, background): “Thus, the last decade has seen a growing interest in alternative representations of biodiversity, including phylogenetic diversity (PD) and functional diversity (FD) (Devictor et al., 2010; Meynard et al., 2011; Stegen & Hurlbert, 2011).”
- Ecological drivers of multiple facets of beta diversity in a lentic macroinvertebrate metacommunity (2017, background): “Rather, current ideas emphasize that multiple facets of biodiversity should be considered more fully to provide a clearer picture of spatial patterning of ecological communities (Graham and Fine 2008; Meynard et al. 2011).”
- Impacts of agricultural intensification on bird communities: New insights from a multi-level and multi-facet approach of biodiversity (2016, background): “Agricultural intensification can also affect functional diversity but not necessarily in the same direction as taxonomic diversity, depending on the spatial scale considered (Devictor et al., 2010; Filippi-Codaccioni et al., 2010; Meynard et al., 2011).”