Range shifts and adaptive responses to Quaternary climate change.
By M. Davis, R. Shaw. Science, 2001
2,433 citations recorded by the source corpus.
Subfields: Atmospheric Science, Ecological Modeling, Genetics
View Paper: https://www.semanticscholar.org/paper/8860f8d7c1b2084623cacf71de19eeb902d93b81
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Atmospheric Science
- J. Bradley St. Clair
- Solomon Dobrowski
- D. Nogués-Bravo
- A. Tribsch
- R. Holderegger
- S. Normand
- Wilfried Thuiller
- I. Stehlik
In Ecological Modeling
- Miguel B. Araújo
- A. Townsend Peterson
- Wilfried Thuiller
- Antoine Guisan
- Jorge M. Lobo
- Jane Elith
- Jorge Soberón
- Jens‐Christian Svenning
In Genetics
- A. Townsend Peterson
- Jorge Soberón
- Jorge M. Lobo
- Miguel B. Araújo
- Jane Elith
- A. Jiménez‐Valverde
- Wilfried Thuiller
- E. Martínez‐Meyer
Citations in the corpus
- The Resurrection Initiative: Storing Ancestral Genotypes to Capture Evolution in Action (2008, neutral): “to Capture Evolution in Action”
- Genetic variation in productivity of foundation riparian species at the edge of their distribution: implications for restoration and assisted migration in a warming climate (2011, background): “Studies including a genetic component in climate change models generally show that populations are adapted to a narrow climatic range (Morgenstern, 1996; O’Neill et al., 2008; Wang et al., 2010), outside of which populations are maladapted (Crespi, 2000; Davis & Shaw, 2001; St Clair & Howe, 2007).”
- Deterministic Plio‐Pleistocene extinctions in the European cool‐temperate tree flora (2003, neutral): “Trees often show adaptation to local environmental conditions and such adaptation has probably been of importance during past range expansions (e.g. Davis & Shaw 2001).”
- The role of forest genetic resources in responding to biotic and abiotic factors in the context of anthropogenic climate change (2014, background): “local extirpations (Davis and Shaw, 2001).”
- Use of niche models in invasive species risk assessments (2011, background): “Facilitative interactions, ecological and physiological plasticity, and microevolutionary adaptation may also lead nonnative species to occupy novel environmental conditions in invaded areas (Orr and Smith 1998; Rodro´guez-Trelles and Rodro ´guez 1998; Gomulkiewicz et al. 1999; Davis and Shaw 2001;”
- ORIGINAL ARTICLE: Towards an understanding of the Holocene distribution of Fagus sylvatica L. (2006, background): “It could be argued that the long tails in the F. sylvatica pollen curves and the delayed spread in north-western Europe could also be a result of slow adaptation (Davis & Shaw, 2001).”
- Latitudinal gradients as natural laboratories to infer species' responses to temperature (2013, background): “As a result, patterns of genetic differentiation and local adaptation are expected to differ along latitudinal and altitudinal transects (Davis & Shaw 2001; Jump, M aty as & Pe~nuelas 2009).”
- Genetic maladaptation of coastal Douglas‐fir seedlings to future climates (2007, background): “…populations may adjust to climate change by exhibiting phenotypic plasticity (i.e. altering their biochemistry, physiology, and development in response to environmental change), migrating to new habitats, or evolving in place (Davis & Shaw, 2001; Rehfeldt et al., 2001; Westfall & Millar, 2004).”
- Spatial and interspecific variability in phenological responses to warming temperatures (2009, background): “However, groups of species may vary in their responses to climatic variation across a wide geographical range due to genetic and environmental variation (Davis and Shaw, 2001; Etterson and Shaw, 2001).”
- Ecological niches as stable distributional constraints on mammal species, with implications for Pleistocene extinctions and climate change projections for biodiversity (2004, background): “The degree to which these shifts follow consistent climate regimes (‘ecological niches’, at least at coarse scales), however, has yet to be tested rigorously ( Davis & Shaw, 2001 ).”
- Considerations for restoring temperate forests of tomorrow: forest restoration, assisted migration, and bioengineering (2015, background): “Climate projections indicate trees must migrate more than 3000 m per year, far exceeding their observed annual rates of less than 500 m (Davis and Shaw 2001; Aitken et al. 2008).”
- Eco-evolutionary conservation biology: contemporary evolution and the dynamics of persistence (2007, background): “This could be particularly important in populations facing climate change, where immigrants from southern populations convey adaptive genes into northern populations during a range shift (Pease et al. 1989; Davis & Shaw 2001 ).”
- Geographic variation in the upper thermal limits of an intertidal snail: implications for climate envelope models. (2009, background): “Although some have recognized the importance of heterogeneous tolerances among populations across a species’ range (Davis & Shaw 2001, Harte et al. 2004, Aitken et al. 2008, O’Neill et al. 2008), a common expectation based on a simple latitudinal temperature gradient is that populations from low…”