Relationships between boreal wildfire emissions and day-to-day variations in meteorological variables are complex and have important implications for the sensitivity of high-latitude ecosystems to climate change. We examined the influence of environmental conditions on boreal fire emissions and fire contributions to regional trace gas variability in interior Alaska during the summer of 2013 using two types of analysis. First, we quantified the degree to which meteorological and fire weather indices explained regional variability in fire activity using four different products, including active fires, fire radiative power, burned area, and carbon emissions. Second, we combined daily emissions from the Alaskan Fire Emissions Database (AKFED) with the coupled Polar Weather Research and Forecasting/Stochastic Time-Inverted Lagrangian Transport model to estimate fire contributions to trace gas concentration measurements at the Carbon in Arctic Reservoirs Vulnerability Experiment-NOAA Global Monitoring Division (CRV) tower in interior Alaska. Tower observations during two high fire periods were used to estimate CO and CH4 emission factors. We found that vapor pressure deficit and temperature had a level of performance similar to more complex fire weather indices. Emission factors derived from CRV tower measurements were 134 ± 25 g CO per kg of combusted biomass and 7.74 ± 1.06 g CH4 per kg of combusted biomass. Predicted daily CO mole fractions from AKFED emissions were moderately correlated with CRV observations (r = 0.68) and had a high bias. The modeling system developed here allows for attribution of emission factors to individual fires and has the potential to improve our understanding of regional CO, CH4, and CO2 budgets.

Black carbon (BC) aerosol emitted by boreal fires has the potential to accelerate losses of snow and ice in many areas of the Arctic, yet the importance of this source relative to fossil fuel BC emissions from lower latitudes remains uncertain. Here we present measurements of the isotopic composition of BC and organic carbon (OC) aerosols collected at two locations in interior Alaska during the summer of 2013, as part of NASA's Carbon in Arctic Reservoirs Vulnerability Experiment. We isolated BC from fine air particulate matter (PM2.5) and measured its radiocarbon (Δ14C) content with accelerator mass spectrometry. We show that fires were the dominant contributor to variability in carbonaceous aerosol mass in interior Alaska during the summer by comparing our measurements with satellite data, measurements from an aerosol network and predicted concentrations from a fire inventory coupled to an atmospheric transport model. The Δ14C of BC from boreal fires was 131 ± 52‰ in the year 2013 when the Δ14C of atmospheric CO2 was 23 ± 3‰, corresponding to a mean fuel age of 20 years. Fire-emitted OC had a similar Δ14C (99 ± 21‰) as BC, but during background (low fire) periods OC (45 to 51‰) was more positive than BC (-354 to -57‰). We also analyzed the carbon and nitrogen elemental and stable isotopic composition of the PM2.5. Fire-emitted aerosol had an elevated carbon to nitrogen (C/N) ratio (29 ± 2) and δ15N (16 ± 4‰). Aerosol Δ14C and δ13C measurements were consistent with a mean depth of burning in organic soil horizons of 20 cm (and a range of 8 to 47 cm). Our measurements of fire-emitted BC and PM2.5 composition constrain the end-member of boreal forest fire contributions to aerosol deposition in the Arctic and may ultimately reduce uncertainties related to the impact of a changing boreal fire regime on the climate system.