Tools for integrating range change, extinction risk and climate change information into conservation management
By Damien A. Fordham, H. Resit Akçakaya, Miguel B. Araújo, David A. Keith, Barry W. Brook. 2013
133 citations recorded by the source corpus.
Subfields: Ecological Modeling, Ecology, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/f71215d45cbd690fe19b21d0ad9ea1d6b4dae9f8
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
- Diogo Alagador
- A. Hoffmann
- M. Byrne
- J. Cerdeira
- Miguel B. Araújo
- F. Mark
- Stefan Gößling-Reisemann
- H. Poertner
In Ecology
- Diogo Alagador
- Miguel B. Araújo
- A. Hoffmann
- J. Cerdeira
- F. Mark
- Stefan Gößling-Reisemann
- H. Poertner
- Hauke Reuter
In Nature and Landscape Conservation
- Diogo Alagador
- A. Hoffmann
- J. Cerdeira
- Miguel B. Araújo
- Stefan Gößling-Reisemann
- M. Byrne
- L. Joseph
- F. Mark
Citations in the corpus
- A framework for incorporating evolutionary genomics into biodiversity conservation and management (2015, background): “Whilst uses of such models have been criticised in the past, models that thoroughly account for algorithmic uncertainties, followed by careful interpretation of results, remain useful and widely used tools for forecasting impacts of climate change on large numbers of species [126].”
- Climate change, species range shifts and dispersal corridors: an evaluation of spatial conservation models (2016, methodology): “In an ideal scenario, it would be possible to adequately mechanistically assess persistence of all species of conservation concern and use predictions to define conservation targets (e.g. Fordham et al. 2013b).”
- Modelling climate change impacts on marine fish populations: process-based integration of ocean warming, acidification and other environmental drivers (2016, background): “…it is 462 difficult to include ontogenetic shifts in environmental tolerance or preference in different 463 life stages (Robinson et al., 2011), but more detailed, stage-structured representations of 464 population processes have been achieved in terrestrial models (e.g. Fordham et al., 2013).”