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SMALL‐RODENT DYNAMICS AND PREDATION
Author(s) -
Hanski Ilkka,
Henttonen Heikki,
Korpimäki Erkki,
Oksanen Lauri,
Turchin Peter
Publication year - 2001
Publication title -
ecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.144
H-Index - 294
eISSN - 1939-9170
pISSN - 0012-9658
DOI - 10.1890/0012-9658(2001)082[1505:srdap]2.0.co;2
Subject(s) - predation , population cycle , generalist and specialist species , vole , ecology , rodent , taiga , biology , weasel , microtus , predator , population , boreal , habitat , demography , sociology
The hypothesis that the regular multiannual population oscillations of boreal and arctic small rodents (voles and lemmings) are driven by predation is as old as the scientific study of rodent cycles itself. Subsequently, for several decades, the predation hypothesis fell into disrepute, possibly because the views about predation and rodent dynamics were too simplistic. Here we review the work that has been done on the predation hypothesis primarily in Fennoscandia over the past decade. Models of predator–prey interaction have been constructed for the least weasel ( Mustela nivalis ) and the field vole ( Microtus agrestis ), which are considered to be the key specialist predator and the key prey species in the multispecies communities in the boreal forest region in Fennoscandia. The basic model has been parameterized with independent field data, and it predicts well the main features of the observed dynamics. An extension of the model also including generalist and nomadic avian predators predicts correctly the well‐documented and striking geographic gradient in rodent oscillations in Fennoscandia, with the amplitude and cycle period decreasing from north to south. These geographic changes are attributed to the observed latitudinal change in the density of generalist and nomadic predators, which are expected to have a stabilizing effect on rodent dynamics. We review the other observational, modeling, and experimental results bearing on the predation hypothesis and conclude that it accounts well for the broad patterns in rodent oscillations in Fennoscandia. We discuss the application of the predation hypothesis to other regions in the northern hemisphere. The predation hypothesis does not make predictions about multiannual and latitudinal changes in body size, behavior, and demography of rodents, which may have some population‐dynamic consequences. With the current evidence, however, we consider it unlikely that the phenotypic and genotypic composition of populations would be instrumental for generating the broad patterns in rodent oscillations.