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Coevolution can reverse predator–prey cycles
Edited by Alan Hastings, University of California, Davis, CA, and accepted by the Editorial Board February 10, 2014 (received for review September 18, 2013)

Significance
The abundances of predators and their prey can oscillate in time. Mathematical theory of predator–prey systems predicts that in predator–prey cycles, peaks in prey abundance precede peaks in predator abundance. However, these models do not consider how the evolution of predator and prey traits related to offense and defense will affect the ordering and timing of peaks. Here we show that predator–prey coevolution can effectively reverse the ordering of peaks in predator–prey cycles, i.e., peaks in predator abundance precede peaks in prey abundance. We present examples from three distinct systems that exhibit reversed cycles, suggesting that coevolution may be an important driver of cycles in those systems.
Abstract
A hallmark of Lotka–Volterra models, and other ecological models of predator–prey interactions, is that in predator–prey cycles, peaks in prey abundance precede peaks in predator abundance. Such models typically assume that species life history traits are fixed over ecologically relevant time scales. However, the coevolution of predator and prey traits has been shown to alter the community dynamics of natural systems, leading to novel dynamics including antiphase and cryptic cycles. Here, using an eco-coevolutionary model, we show that predator–prey coevolution can also drive population cycles where the opposite of canonical Lotka–Volterra oscillations occurs: predator peaks precede prey peaks. These reversed cycles arise when selection favors extreme phenotypes, predator offense is costly, and prey defense is effective against low-offense predators. We present multiple datasets from phage–cholera, mink–muskrat, and gyrfalcon–rock ptarmigan systems that exhibit reversed-peak ordering. Our results suggest that such cycles are a potential signature of predator–prey coevolution and reveal unique ways in which predator–prey coevolution can shape, and possibly reverse, community dynamics.
Footnotes
- ↵1To whom correspondence should be addressed. E-mail: michael.cortez{at}biology.gatech.edu.
Author contributions: M.H.C. designed research; M.H.C. performed research; M.H.C. contributed new reagents/analytic tools; M.H.C. and J.S.W. analyzed data; and M.H.C. and J.S.W. wrote the paper.
The authors declare no conflict of interest.
This article is a PNAS Direct Submission. A.H. is a guest editor invited by the Editorial Board.
This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1317693111/-/DCSupplemental.