Gradients in density variations of small rodents – the importance of latitude and snow cover
Summary. Microtine rodents are known to show extreme population variations (cycles) but non-cyclic populations have also been recognized uring recent years. The cyclic populations have been widely thought o be regulated by intrinsic mechanisms. However, such predictions for cyclic populations are us...
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| Format: | Text |
| Language: | English |
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1985
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| Online Access: | http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.591.1346 http://www.arctic-predators.uit.no/biblio_IPYappl/HanssonOecologia85 gradients density variations snow cover.pdf |
| Summary: | Summary. Microtine rodents are known to show extreme population variations (cycles) but non-cyclic populations have also been recognized uring recent years. The cyclic populations have been widely thought o be regulated by intrinsic mechanisms. However, such predictions for cyclic populations are usually not applicable to non-cyclic ones and extrinsic factors may have to be included in any expla-nation. A hypothesis that the degree of fluctuations in small rodent numbers is related to the sustainable number of gen-eralist predators was tested on mainly literature data by computing "indices of cyclicity " for local populations. These indices were related to latitude and snow cover (two measures) as these variables will affect he amount of alter-native prey available for these generalists. Within Fenno-scandia such indices for Clethrionomys glareolus and Micro-tus agrestis were clearly positively related to latitude and snow cover. The fraction of populations with summer de-clines in numbers, characterizing highly cyclic populations, increased in the same way. Cyclicity indices in Great Britain were similar to those in southern Fennoscandia, both areas being poor in snow, but were higher at the same latitudes in eastern Europe with more snow. Indices of density varia-tions were generally low in North American Clethrionomys species and very variable in Microtus species. The gradients observed and differences between conti-nents are interpreted as due to microtine-vegetation interac-tions in northern European areas poor in generalist preda-tors but with important small mustelid predation, and to similar snowshoe hare-vegetation i teractions in mainly Canada-Alaska, where small rodents may serve as alterna-tive prey for numerically fluctuating hare predators, at least in the forests. Western European microtine populations, and probably many others, seem to be regulated by general-ist predators. 1. |
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