Species–area relationships always overestimate extinction rates from habitat loss (original) (raw)
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- Published: 18 May 2011
Nature volume 473, pages 368–371 (2011) Cite this article
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Abstract
Extinction from habitat loss is the signature conservation problem of the twenty-first century1. Despite its importance, estimating extinction rates is still highly uncertain because no proven direct methods or reliable data exist for verifying extinctions. The most widely used indirect method is to estimate extinction rates by reversing the species–area accumulation curve, extrapolating backwards to smaller areas to calculate expected species loss. Estimates of extinction rates based on this method are almost always much higher than those actually observed2,3,4,5. This discrepancy gave rise to the concept of an ‘extinction debt’, referring to species ‘committed to extinction’ owing to habitat loss and reduced population size but not yet extinct during a non-equilibrium period6,7. Here we show that the extinction debt as currently defined is largely a sampling artefact due to an unrecognized difference between the underlying sampling problems when constructing a species–area relationship (SAR) and when extrapolating species extinction from habitat loss. The key mathematical result is that the area required to remove the last individual of a species (extinction) is larger, almost always much larger, than the sample area needed to encounter the first individual of a species, irrespective of species distribution and spatial scale. We illustrate these results with data from a global network of large, mapped forest plots and ranges of passerine bird species in the continental USA; and we show that overestimation can be greater than 160%. Although we conclude that extinctions caused by habitat loss require greater loss of habitat than previously thought, our results must not lead to complacency about extinction due to habitat loss, which is a real and growing threat.
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Figure 1: Sampling differences for SAR and EAR.

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Figure 2: Species– and endemics–area curves for six of the nine data sets in Table 1 .

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Acknowledgements
We acknowledge the work of the principal investigators and their field assistants for collecting the field data on the large plots of the Center for Tropical Forest Science network. We are grateful to P. Gowaty, K. Gaston and M. Rosenzweig for their comments on the paper. We thank R. Condit, R. Perez and S. Agular for Barro Colorado Island, R. Valencia for Yasuni, N. Supardi Noor and R. Kassim for Pasoh, D. Thomas, D. Kenfack and G. Chuyong for Korup, W.-H. Ye for Dinghushan, I.-F. Sun and C.-F. Hseih for Fushan, X.-H. Wang for Tiantong, Z.-Q. Hao for Changbaishan and X.-L. Wang for processing the passerine data. This work was supported by Sun Yat-sen University, the Natural Sciences and Engineering Research Council (Canada), NASA (National Aeronautics and Space Administration) and the US National Science Foundation.
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Authors and Affiliations
- State Key Laboratory of Biocontrol and School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, China
Fangliang He - Department of Renewable Resources, University of Alberta, Edmonton, Alberta, T6G 2H1, Canada,
Fangliang He - Department of Ecology and Evolutionary Biology, University of California, Los Angeles, 90095, California, USA
Stephen P. Hubbell - Center for Tropical Forest Science, Smithsonian Tropical Research Institute, Unit 0948, APO AA 34002-0948, Republic of Panama ,
Stephen P. Hubbell
Authors
- Fangliang He
- Stephen P. Hubbell
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Both authors designed the study, analysed and interpreted data, and wrote the paper.
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Correspondence toFangliang He or Stephen P. Hubbell.
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The authors declare no competing financial interests.
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He, F., Hubbell, S. Species–area relationships always overestimate extinction rates from habitat loss.Nature 473, 368–371 (2011). https://doi.org/10.1038/nature09985
- Received: 21 December 2010
- Accepted: 08 March 2011
- Published: 18 May 2011
- Issue date: 19 May 2011
- DOI: https://doi.org/10.1038/nature09985
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- Suresh Babu 22 May 2011, 16:15
Although this article deals with a better way to measure extinction rates (of which a score of methods are already debated) than the reverse SAR, it has been made to sound as though it is a scientific breakthrough. The flaws with the classical approach has been known and debated. Serious concerns remain in their adopting 'the last individual' of a species as the object of conservation. It is now well understood that a breeding population of a minimum size is necessary for the survival of a species. When we take this minimum viable population in to consideration, the new extinction rates are likely to be 'gross under-estimates'. Besides, the new estimates would put the present extinction rates at 40-400 or 4000 times the background rates, without factoring in minimum viable populations that grossly vary across taxa, which is hardly a relief. If only we could devise a model to plug that model in to this one, we could come up with an even better model of how habitat destruction impacts species extinctions. We need to, at some point begin to question the relevance of these all pervasive, unifying macro-models and the manner in which they crumble at the sight of reality.
Editorial Summary
Getting a handle on extinction rates
There is broad agreement that Earth is facing a biodiversity crisis, but estimating extinction rates remains a daunting task, not least because it is almost impossible to determine when the very last individual of a species has died. Fangliang He and Stephen Hubbell demonstrate that a widely used indirect method of estimating extinction rates — based on backward extrapolation of species–area relationship data — tends to overestimate the problem. As an example, they cite data on passerine bird species in the United States. He and Hubbell stress that habitat loss remains a real and growing threat to biodiversity, although we need to develop more reliable means of monitoring the situation.