Ecological niche modelling of two cryptic bat species calls for a reassessment of their conservation status

By Thomas Sattler, F. Bontadina, A. Hirzel, R. Arlettaz. 2007

189 citations recorded by the source corpus.

Subfields: Ecological Modeling, Ecology, Ecology, Evolution, Behavior and Systematics

View Paper: https://www.semanticscholar.org/paper/cb502448f753fd31b80f28d29faa9e546a22ac15

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

In Ecology

In Ecology, Evolution, Behavior and Systematics

Citations in the corpus

Moving in three dimensions: effects of structural complexity on occurrence and activity of insectivorous bats in managed forest stands (2012, background): “Both species are nearly identical in wing morphology and foraging behaviour, but they are known to differ in their use of forest habitats (e.g. DavidsonWatts, Walls & Jones 2006; Sattler et al. 2007).”
The projected effects of climatic and vegetation changes on the distribution and diversity of Southeast Asian bats (2012, background): “The identification of these cryptic species may prove key to their future conservation (Sattler et al., 2007), as many currently unrecognized taxa are currently assigned lower levels of conservation status than may be warranted.”
Ground validation of presence‐only modelling with rare species: a case study on barbastelles Barbastella barbastellus (Chiroptera: Vespertilionidae) (2010, background): “…productive when addressing issues such as planning field surveys, defining reintroduction areas, identifying population fragmentation, planning rapid biodiversity assessments in poorly documented regions and supporting a wide range of conservation strategies or policies (Sattler et al. 2007).”
Niche Breadth: Causes and Consequences for Ecology, Evolution, and Conservation (2020, background): “In contrast, species that are both scarce and have a narrow range of habitat affinities will be more vulnerable to acute perturbations such as point-source pollution, a species’ invasion, or local land-use change (Sattler et al. 2007).”
Habitat suitability modelling and niche theory (2008, methodology): “In particular, niche theory provides many niche overlap measures (e.g. Hurlbert 1978) that have still to be ported to the HSM world (but see Sattler et al .”
Effects of landscape-scale broadleaved woodland configuration and extent on roost location for six bat species across the UK (2011, background): “pygmaeus and water features seen in studies of foraging associations (Davidson-Watts et al., 2006; Downs and Racey, 2006; Nicholls and Racey, 2006b; Sattler et al., 2007) extends to the selection of roost location.”
Bats and Water: Anthropogenic Alterations Threaten Global Bat Populations (2016, background): “2000) and allowing interspecific niche partitioning and thus coexistence (Oakeley and Jones 1998; Nicholls and Racey 2006; DavidsonWatts et al. 2006; Sattler et al. 2007).”
Carnivore biodiversity in Tanzania: revealing the distribution patterns of secretive mammals using camera traps (2010, methodology): “We computed three presence-only evaluation measures, that is absolute validation index (AVI), contrast validation index (CVI; Sattler et al., 2007) and continuous Boyce’s index (BI; Hirzel et al., 2006).”
Differential impact of landscape transformation on pumas (Puma concolor) and jaguars (Panthera onca) in the Upper Paraná Atlantic Forest (2011, methodology): “, 2002) and that its results allow a direct comparison among multiple species that inhabit the same region by interpreting the parameters from the ecological niche perspective (e.g. their relative specialization level; Chefaoui et al., 2005; Acevedo et al., 2007; Sattler et al., 2007; Durant et al.,”
Landscape connectivity, habitat structure and activity of bat guilds in farmland-dominated matrices (2013, unknown): “pipistrellus, as was expected (Sattler et al. 2007), given it is a generalist species (Davidson-Watts, Walls & Jones 2006).”