AVAILABILITY OF FOOD AND THE POPULATION DYNAMICS OF ARVICOLINE RODENTS

By Peter Turchin, G. O. Batzli. 2001

186 citations recorded by the source corpus.

Subfields: Ecology, Nature and Landscape Conservation, Public Health, Environmental and Occupational Health

View Paper: https://www.semanticscholar.org/paper/0988a9ce0da061319f3028dcb6342b09c92ae29a

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology

1. Evelyn H. Merrill
2. D. Fortin
3. Jacqui Frair
4. Daniel T. Haydon
5. J. Morales
6. P. Banks
7. Lauri Oksanen
8. J. Olofsson

In Nature and Landscape Conservation

1. D. Fortin
2. Evelyn H. Merrill
3. Daniel T. Haydon
4. P. Banks
5. J. Morales
6. Jacqui Frair
7. T. Oksanen
8. Peter Turchin

In Public Health, Environmental and Occupational Health

1. Peter Turchin
2. Lauri Oksanen
3. R. Ims
4. E. Fuglei
5. T. Oksanen
6. E. Korpimäki
7. J. Olofsson
8. Jonas Dahlgren

Citations in the corpus

• Landscape scale, heterogeneity, and the viability of Serengeti grazers (2005, methodology): “Similar logic has been used to model grassland dynamics in the face of grazing by voles (Turchin & Batzli 2001).”
• Arctic lemmings, Lemmus spp. and Dicrostonyx spp.: integrating ecological and evolutionary perspectives (2008, methodology): “The Barrow model of Turchin and Batzli (2001), which focuses on brown lemmings, differs from the simple arvicoline–plant model by assuming that lemmings also have annually renewed resources, uninfluenced by past herbivory (e.g. graminoids, sprouting from subterranean rhizomes).”
• Adaptive models for large herbivore movements in heterogeneous landscapes (2005, methodology): “The modeling of plant growth dynamics was based on a modified version of (Turchin and Batzli 2001) regrowth model.”
• Can Reindeer Overabundance Cause a Trophic Cascade? (2007, background): “Because food limitation in small rodents is expected to kick in at the culmination of the peak phase ( Turchin and Batzli 2001 ), the timing of our study was ideal with respect to testing for effects of reindeer overabundance on small rodent populations.”
• Vole cycles and predation in temperate and boreal zones of Europe (2005, background): “2000; Ekerholm, Oksanen & Oksanen 2001; Turchin & Batzli 2001) suggest that even the arvicoline rodent cycles at high latitudes may be a heterogeneous phenomenon, where different trophic interactions account for different cycles.”
• SMALL‐RODENT DYNAMICS AND PREDATION (2001, methodology): “…(1971, 1977; see also Rosenzweig and MacArthur 1963), applied by Oksanen (1990) to rodent–predator dynamics, and the model of Leslie (1948) and May (1973), first used by Hanski et al. (1991) to model vole–weasel dynamics, have major structural differences (see also Turchin and Batzli 2001).”
• A rodent plague on prairie diversity (2002, background): “Microtines show 10-fold pulses of abundance with a periodicity of 3±6 years (Taitt & Krebs 1985), whether predation, resource depletion, chaos, or some dynamic mix of factors drives rodent ¯uctuations (Turchin & Ellner 2000; Turchin & Batzli 2001).”
• Trophic Interaction Cycles in Tundra Ecosystems and the Impact of Climate Change (2005, methodology): “Both types of compounds, at least in theory, can create multiannual population cycles in herbivore populations, if the induced response in plants operates with a time delay ( Turchin and Batzli 2001 ).”