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This data describes above-ground and below-ground variables collected under small mammal-built structures and control sites from two tundra locations in polygonal tundra near Utqiagvik, Alaska, USA. Small mammal structures sampled included hay piles (winter nests), runways, latrines, and burrow entrances. Above-ground data collected include relative percent cover, litter depth, and Normalized Difference Vegetation Index. Below-ground data collected include inorganic soil nutrients, total extractable soil nutrients, microbial biomass nutrients, microbial exo-enzyme activities, soil pH, soil conductivity, soil temperature, and soil respiration. 

We use a simple model of coupled carbon and nitrogen cycles in terrestrial ecosystems to examine how explicitly representing grazers versus having grazer effects implicitly aggregated in with other biogeochemical processes in the model alters predicted responses to elevated carbon dioxide and warming. The aggregated approach can affect model predictions because grazer-mediated processes can respond differently to changes in climate from the processes with which they are typically aggregated. We use small-mammal grazers in arctic tundra as an example and find that the typical three-to-four-year cycling frequency is too fast for the effects of cycle peaks and troughs to be fully manifested in the ecosystem biogeochemistry. We conclude that implicitly aggregating the effects of small-mammal grazers with other processes results in an underestimation of ecosystem response to climate change relative to estimations in which the grazer effects are explicitly represented. The magnitude of this underestimation increases with grazer density. We therefore recommend that grazing effects be incorporated explicitly when applying models of ecosystem response to global change. 

We use a simple model of coupled carbon and nitrogen cycles in terrestrial ecosystems to examine how explicitly representing grazers versus having grazer effects implicitly aggregated in with other biogeochemical processes in the model alters predicted responses to elevated carbon dioxide and warming. The aggregated approach can affect model predictions because grazer-mediated processes can respond differently to changes in climate from the processes with which they are typically aggregated. We use small-mammal grazers in arctic tundra as an example and find that the typical three-to-four-year cycling frequency is too fast for the effects of cycle peaks and troughs to be fully manifested in the ecosystem biogeochemistry. We conclude that implicitly aggregating the effects of small-mammal grazers with other processes results in an underestimation of ecosystem response to climate change relative to estimations in which the grazer effects are explicitly represented. The magnitude of this underestimation increases with grazer density. We therefore recommend that grazing effects be incorporated explicitly when applying models of ecosystem response to global change. 

Small mammals (rodents and shrews) were sampled 7-12 years following the Anaktuvuk River Fire to examine how post-fire ecological changes influence small mammal abundance. Small mammals were snap-trapped in August 2014, 2017-2019 at the site of the 2007 Anaktuvuk River Fire, and a nearby unburned control site. At each site, 120 traps were set in 3 parallel lines spaced 40m apart. Each trap was spaced 10m apart, baited, and set to rodent sign within one meter of the trap station. Traps were checked the following two mornings with all captures collected and sprung traps reset. Abundance estimates (captures per 100 trap nights) are presented for tundra voles (Microtus oeconomus), red-backed voles (Myodes rutilus) and shrews (Sorex spp.) The goals of the project were to examine the impact of post-fire changes in plant community composition and structure on habitat suitability and rodent herbivore activity in response to a large, severe, and unprecedented fire in northern Alaska moist acidic tundra.