Warming of the Arctic can stimulate microbial decomposition and release of permafrost soil carbon (C) as greenhouse gases, and thus has the potential to influence climate change. At the same time, plant growth can be stimulated and offset C release. This study presents a 15‐year time series comprising chamber and eddy covariance measurements of net ecosystem C exchange in a tundra ecosystem in Alaska where permafrost has been degrading due to regional warming. The site was a carbon dioxide source to the atmosphere with a cumulative total loss of 781.6 g C m−2 over the study period. Both gross primary productivity (GPP) and ecosystem respiration (Reco) were already likely higher than historical levels such that increases in Reco losses overwhelmed GPP gains in most years. This shift to a net C source to the atmosphere likely started in the early 1990s when permafrost was observed to warm and thaw at the site. Shifts in the plant community occur more slowly and are likely to constrain future GPP increases as compared to more rapid shifts in the microbial community that contribute to increased Reco. Observed rates suggest that cumulative net soil C loss of 4.18–10.00 kg C m−2—8%–20% of the current active layer soil C pool—could occur from 2020 to the end of the century. This amount of permafrost C loss to the atmosphere represents a significant accelerating feedback to climate change if it were to occur at a similar magnitude across the permafrost region.
Permafrost formation and degradation creates a highly patchy mosaic of boreal peatland ecosystems in Alaska driven by climate, fire, and ecological changes. To assess the biophysical factors affecting permafrost dynamics, we monitored permafrost and ecological conditions in central Alaska from 2005 to 2021 by measuring weather, land cover, topography, thaw depths, hydrology, soil properties, soil thermal regimes, and vegetation cover between burned (1990 fire) and unburned terrain. Climate data show large variations among years with occasional, extremely warm–wet summers and cold–snowless winters that affect permafrost stability. Microtopography and thaw depth surveys revealed both permafrost degradation and aggradation. Thaw depths were deeper in post-fire scrub compared to unburned black spruce and increased moderately during the last year, but analysis of historical imagery (1954–2019) revealed no increase in thermokarst rates due to fire. Recent permafrost formation was observed in older bogs due to an extremely cold–snowless winter in 2007. Soil sampling found peat extended to depths of 1.5–2.8 m with basal radiocarbon dates of ~5–7 ka bp, newly accumulating post-thermokarst peat, and evidence of repeated episodes of permafrost formation and degradation. Soil surface temperatures in post-fire scrub bogs were ~1 °C warmer than in undisturbed black spruce bogs, and thermokarst bogs and lakes were 3–5 °C warmer than black spruce bogs. Vegetation showed modest change after fire and large transformations after thermokarst. We conclude that extreme seasonal weather, ecological succession, fire, and a legacy of earlier geomorphic processes all affect the repeated formation and degradation of permafrost, and thus create a highly patchy mosaic of ecotypes resulting from widely varying ecological trajectories within boreal peatland ecosystems.
As climate change accelerates in northern latitudes, there is an increasing need to understand the role of climate in influencing predator-prey systems. We investigated wolf population dynamics and numerical response in Denali National Park and Preserve in Alaska, United States from 1986 to 2016 under a long-term range of varying climatic conditions and in the context of prey vulnerability, abundance, and population structure using an integrated population modeling approach. We found that wolf natality, or the number of wolves added to packs, increased with higher caribou population size, calf:cow ratio, and hare numbers, responding to a 1-year lag. Apparent survival increased in years with higher calf:cow ratios and cumulative snowfall in the prior winter, indicators of a vulnerable prey base. Thus, indices of prey abundance and vulnerability led to responses in wolf demographics, but we did not find that the wolf population responded numerically. During recent caribou and moose population increases wolf natality increased yet wolf population size declined. The decline in wolf population size is attributed to fewer packs in recent years with a few very large packs as opposed to several packs of comparable size. Our results suggest that territoriality can play a vital role in our study area on regulating population growth. These results provide a baseline comparison of wolf responses to climatic and prey variability in an area with relatively low levels of human disturbance, a rare feature in wolf habitat worldwide.
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