USE AND INTERPRETATION OF LOGISTIC REGRESSION IN HABITAT-SELECTION STUDIES
By K. Keating, S. Cherry. 2004
595 citations recorded by the source corpus.
Subfields: Ecology, Small Animals, Statistics and Probability
View Paper: https://www.semanticscholar.org/paper/48abc6a2c81a8026c24346d6153d645e334551da
How researchers see this paper
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In Ecology
- Jane Elith
- Antoine Guisan
- A. Townsend Peterson
- Rune Halvorsen
- Jorge Soberón
- Wilfried Thuiller
- M. Boyce
- Miguel B. Araújo
In Small Animals
- J. Fieberg
- M. Boyce
- Mark Hebblewhite
- Jason Matthiopoulos
- K. Wilson
- G. Blouin‐Demers
- T. O'Shea
- Miroslav Dud'ik
In Statistics and Probability
- Jane Elith
- Antoine Guisan
- J. Leathwick
- J. Pearce
- A. Townsend Peterson
- Jorge Soberón
- Simon C. Barry
- J. Kie
Citations in the corpus
- Variation in niche and distribution model performance: The need for a priori assessment of key causal factors (2012, background): “Much theory (Keating and Cherry, 2004; Pearce and Boyce, 2006; Phillips et al., 2009; Ward et al., 2009; Li et al., 2011) and data (Brotons et al.”
- Climate change‐linked range expansion of Nathusius’ pipistrelle bat, Pipistrellus nathusii (Keyserling & Blasius, 1839) (2010, background): “This is an important distinction when interpreting models based on records that do not result from full surveys of all possible locations (Keating & Cherry, 2004).”
- Protected areas network is not adequate to protect a critically endangered East Africa Chelonian: Modelling distribution of pancake tortoise, Malacochersus tornieri under current and future climates (2020, background): “Such models are commonly referred to as the resource selection functions in the habitat suitability literature (Manly et al. 2002, Keating and Cherry 2004, Johnson et al. 2006).”
- Error and uncertainty in habitat models (2006, methodology): “The most statistically accurate way to model with pseudo-absence data is through the use of specialized models such as case control ( Keating & Cherry 2004; Pearce and Boyce 2006) and resource selection functions (Manly et al. 2002).”
- Human Activity Differentially Redistributes Large Mammals in the Canadian Rockies National Parks (2011, methodology): “…the recommended method for evaluating resource selection because it appropriately measures availability from a mechanistically biological perspective (Moorcroft and Barnett 2008), and results in robust relative probabilities of selection in a used-availability design (Keating and Cherry 2004).”
- Sample selection bias and presence-only distribution models: implications for background and pseudo-absence data. (2009, methodology): “We first investigate how to interpret models produced with random background, using the theory of use–availability sampling in habitat-selection studies (Keating and Cherry 2004).”
- Niche and area of distribution modeling: a population ecology perspective (2010, methodology): “When unbiased absence data are available, correlative methods can be used to estimate the probability P (Y 1j ej ) of the species being present (Y 1), conditioned to environmental information e j (Guisan and Zimmermann 2000, Keating and Cherry 2004, Phillips et al. 2009).”
- Study Designs and Tests for Comparing Resource Use and Availability II (2006, methodology): “For studies that used logistic regression, we identified the data type (see Keating and Cherry 2004) employed: single sample, case control (used–unused), use–availability, or paired use– availability.”
- Modeling of species distributions with Maxent: new extensions and a comprehensive evaluation (2008, background): “Perhaps more importantly, when used on presence-only data, regression-based methods suffer from the problem of ‘‘contaminated controls’’ (Keating and Cherry 2004), in Table 6.”
- Accounting for animal movement in estimation of resource selection functions: sampling and data analysis. (2009, methodology): “For details on how we accounted for autocorrelation in the regression procedure and for the computation of robust standard errors of the selection coefficient estimates, see Appendix C.”
- Accounting for spatially biased sampling effort in presence‐only species distribution modelling (2015, methodology): “Based on occurrence localities of rare (i.e. NatureServe S1- to S3-ranked; NatureServe, 2013) species of vascular plants, bryophytes and butterflies, the probability of sampling was estimated for each taxonomic group across Alberta using logistic regression (Keating & Cherry, 2004).”
- Linking moose habitat selection to limiting factors (2005, unknown): “importance of habitat types (Keating and Cherry 2004).”
- Modelling distribution and abundance with presence‐only data (2006, methodology): “Models estimated using case‐control logistic regression are based on the contrasts between used and control resource units and can be interpreted as odds ratios or relative likelihoods of occurrence ( Keating & Cherry 2004 ).”
- Scale for resource selection functions (2006, methodology): “A special case of presence/absence is the case-control design where intensity of sampling of used and unused resource units is not random (Keating & Cherry, 2004).”
- Resting structures and resting habitat of fishers in the southern Sierra Nevada, California (2009, methodology): “…by the unknown constant pr, and since we are interested only in the relationship between the response and the explanatory variables, we modeled logit(gi) as a linear regression model treating the intercept as a nuisance parameter (for more details see Manly et al., 1993; Keating and Cherry, 2004).”
- Predicting species distributions from museum and herbarium records using multiresponse models fitted with multivariate adaptive regression splines (2007, methodology): “Case-control regression that takes account of contaminated zeros is one example of this (Keating & Cherry, 2004; Pearce & Boyce, 2006), and relevant software for dealing with typical ecological applications is in development (Simon Barry, Gill Ward, pers.comm.).”