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  1. Abstract

    In arctic tundra, large and small mammalian herbivores have substantial impacts on the vegetation community and consequently can affect the magnitude of carbon cycling. However, herbivores are often absent from modern carbon cycle models, partly because relatively few field studies focus on herbivore impacts on carbon cycling. Our objectives were to quantify the impact of 21 years of large herbivore and large and small herbivore exclusion on carbon cycling during peak growing season in a dry heath tundra community. When herbivores were excluded, we observed a significantly greater leaf area index as well as greater vascular plant abundance. While we did not observe significant differences in deciduous dwarf shrub abundance across treatments, evergreen dwarf shrub abundance was greater where large and small herbivores were excluded. Both foliose and fruticose lichen abundance were higher in the large herbivore, but not the small and large herbivore exclosures. Net ecosystem exchange (NEE) likewise indicated the highest carbon uptake in the exclosure treatments and lowest uptake in the control (CT), suggesting that herbivory decreased the capacity of dry heath tundra to take up carbon. Moreover, our calculated NEE for average light and temperature conditions for July 2017, when our measurements were taken, indicated that the tundra was a carbon source in CT, but was a carbon sink in both exclosure treatments, indicating removal of grazing pressure can change the carbon balance of dry heath tundra. Collectively, these findings suggest that herbivore absence can lead to changes in plant community structure of dry heath tundra that in turn can increase its capacity to take up carbon.

     
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  2. Vegetation (species) abundances were measured from LTER heath tundra herbivore exclosures using the point frame method. This file contains the number of pin hits per species for each subplot. 
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  3. Ecosystem carbon dioxide (CO2) flux light response curves were measured from Arctic LTER heath tundra herbivore exclosures. Plot photographs were taken of each subplot using five consumer grade red, green and blue (RGB) wavelength camera. Structure from motion (SFM) photogrammetric method was then used to derive canopy structure. This file contains the CO2, normalized difference vegetation index (NDVI) data and photographs for each plot. 
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  4. Percent cover of tundra vole and brown lemming structures collected from within the Team Vole enclosure/exclosure fences near Nome, Toolik, Utqiagvik, AK 2019. 
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  5. Soil and plant sampling analysis under small mammal-built structures and controls sites from near the Team Vole fences: Nome, Toolik, Utqiagvik, AK 2018-2020. 
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  6. 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. 
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  7. 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. 
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  8. 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. 
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  9. 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. 
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