R. Commane

Cold season emissions dominate the Arctic tundra methane budget

Significance Arctic ecosystems are major global sources of methane. We report that emissions during the cold season (September to May) contribute ≥50% of annual sources of methane from Alaskan tundra, based on fluxes obtained from eddy covariance sites and from regional fluxes calculated from aircraft data. The largest emissions were observed at the driest site (<5% inundation). Emissions of methane in the cold season are linked to the extended “zero curtain” period, where soil temperatures are poised near 0 °C, indicating that total emissions are very sensitive to soil climate and related factors, such as snow depth. The dominance of late season emissions, sensitivity to soil conditions, and importance of dry tundra are not currently simulated in most global climate models. Arctic terrestrial ecosystems are major global sources of methane (CH4); hence, it is important to understand the seasonal and climatic controls on CH4 emissions from these systems. Here, we report year-round CH4 emissions from Alaskan Arctic tundra eddy flux sites and regional fluxes derived from aircraft data. We find that emissions during the cold season (September to May) account for ≥50% of the annual CH4 flux, with the highest emissions from noninundated upland tundra. A major fraction of cold season emissions occur during the “zero curtain” period, when subsurface soil temperatures are poised near 0 °C. The zero curtain may persist longer than the growing season, and CH4 emissions are enhanced when the duration is extended by a deep thawed layer as can occur with thick snow cover. Regional scale fluxes of CH4 derived from aircraft data demonstrate the large spatial extent of late season CH4 emissions. Scaled to the circumpolar Arctic, cold season fluxes from tundra total 12 ± 5 (95% confidence interval) Tg CH4 y−1, ∼25% of global emissions from extratropical wetlands, or ∼6% of total global wetland methane emissions. The dominance of late-season emissions, sensitivity to soil environmental conditions, and importance of dry tundra are not currently simulated in most global climate models. Because Arctic warming disproportionally impacts the cold season, our results suggest that higher cold-season CH4 emissions will result from observed and predicted increases in snow thickness, active layer depth, and soil temperature, representing important positive feedbacks on climate warming.

Carbon dioxide sources from Alaska driven by increasing early winter respiration from Arctic tundra

Significance Rising arctic temperatures could mobilize reservoirs of soil organic carbon trapped in permafrost. We present the first quantitative evidence for large, regional-scale early winter respiration flux, which more than offsets carbon uptake in summer in the Arctic. Data from the National Oceanic and Atmospheric Administration’s Barrow station indicate that October through December emissions of CO2 from surrounding tundra increased by 73% since 1975, supporting the view that rising temperatures have made Arctic ecosystems a net source of CO2. It has been known for over 50 y that tundra soils remain unfrozen and biologically active in early winter, yet many Earth System Models do not correctly represent this phenomenon or the associated CO2 emissions, and hence they underestimate current, and likely future, CO2 emissions under climate change. High-latitude ecosystems have the capacity to release large amounts of carbon dioxide (CO2) to the atmosphere in response to increasing temperatures, representing a potentially significant positive feedback within the climate system. Here, we combine aircraft and tower observations of atmospheric CO2 with remote sensing data and meteorological products to derive temporally and spatially resolved year-round CO2 fluxes across Alaska during 2012–2014. We find that tundra ecosystems were a net source of CO2 to the atmosphere annually, with especially high rates of respiration during early winter (October through December). Long-term records at Barrow, AK, suggest that CO2 emission rates from North Slope tundra have increased during the October through December period by 73% ± 11% since 1975, and are correlated with rising summer temperatures. Together, these results imply increasing early winter respiration and net annual emission of CO2 in Alaska, in response to climate warming. Our results provide evidence that the decadal-scale increase in the amplitude of the CO2 seasonal cycle may be linked with increasing biogenic emissions in the Arctic, following the growing season. Early winter respiration was not well simulated by the Earth System Models used to forecast future carbon fluxes in recent climate assessments. Therefore, these assessments may underestimate the carbon release from Arctic soils in response to a warming climate.

Seasonal fluxes of carbonyl sulfide in a midlatitude forest

Significance The flux of carbonyl sulfide (OCS) provides a quantitative, independent measure of biospheric activity, especially stomatal conductance and carbon uptake, at the ecosystem scale. We describe the factors controlling the hourly, daily, and seasonal fluxes of OCS based on 1 year of observations in a forest ecosystem. Vegetation dominated uptake of OCS, with daytime fluxes accounting for 72% of the total uptake for the year. Nighttime fluxes had contributions from both incompletely closed stomata and soils. Net OCS emission was observed at high temperature in summer. Diurnal and seasonal variations in OCS flux show variable stoichiometry relative to photosynthetic uptake of CO2. An effective model framework is shown, using an explicit representation of ecosystem processing of OCS. Carbonyl sulfide (OCS), the most abundant sulfur gas in the atmosphere, has a summer minimum associated with uptake by vegetation and soils, closely correlated with CO2. We report the first direct measurements to our knowledge of the ecosystem flux of OCS throughout an annual cycle, at a mixed temperate forest. The forest took up OCS during most of the growing season with an overall uptake of 1.36 ± 0.01 mol OCS per ha (43.5 ± 0.5 g S per ha, 95% confidence intervals) for the year. Daytime fluxes accounted for 72% of total uptake. Both soils and incompletely closed stomata in the canopy contributed to nighttime fluxes. Unexpected net OCS emission occurred during the warmest weeks in summer. Many requirements necessary to use fluxes of OCS as a simple estimate of photosynthesis were not met because OCS fluxes did not have a constant relationship with photosynthesis throughout an entire day or over the entire year. However, OCS fluxes provide a direct measure of ecosystem-scale stomatal conductance and mesophyll function, without relying on measures of soil evaporation or leaf temperature, and reveal previously unseen heterogeneity of forest canopy processes. Observations of OCS flux provide powerful, independent means to test and refine land surface and carbon cycle models at the ecosystem scale.

The atmospheric chemistry of trace gases and particulate matter emitted by different land uses in Borneo

We report measurements of atmospheric composition over a tropical rainforest and over a nearby oil palm plantation in Sabah, Borneo. The primary vegetation in each of the two landscapes emits very different amounts and kinds of volatile organic compounds (VOCs), resulting in distinctive VOC fingerprints in the atmospheric boundary layer for both landscapes. VOCs over the Borneo rainforest are dominated by isoprene and its oxidation products, with a significant additional contribution from monoterpenes. Rather than consuming the main atmospheric oxidant, OH, these high concentrations of VOCs appear to maintain OH, as has been observed previously over Amazonia. The boundary-layer characteristics and mixing ratios of VOCs observed over the Borneo rainforest are different to those measured previously over Amazonia. Compared with the Bornean rainforest, air over the oil palm plantation contains much more isoprene, monoterpenes are relatively less important, and the flower scent, estragole, is prominent. Concentrations of nitrogen oxides are greater above the agro-industrial oil palm landscape than over the rainforest, and this leads to changes in some secondary pollutant mixing ratios (but not, currently, differences in ozone). Secondary organic aerosol over both landscapes shows a significant contribution from isoprene. Primary biological aerosol dominates the super-micrometre aerosol over the rainforest and is likely to be sensitive to land-use change, since the fungal source of the bioaerosol is closely linked to above-ground biodiversity.

Tundra photosynthesis captured by satellite-observed solar-induced chlorophyll fluorescence

Accurately quantifying the timing and magnitude of respiration and photosynthesis by high-latitude ecosystems is important for understanding how a warming climate influences global carbon cycling. Data-driven estimates of photosynthesis across Arctic regions often rely on satellite-derived enhanced vegetation index (EVI); we find that satellite observations of solar-induced chlorophyll fluorescence (SIF) provide a more direct proxy for photosynthesis. We model Alaskan tundra CO2 cycling (2012–2014) according to temperature and shortwave radiation, and alternately input EVI or SIF to prescribe the annual seasonal cycle of photosynthesis. We find that EVI-based seasonality indicates spring “green-up” to occur nine days prior to SIF-based estimates, and that SIF-based estimates agree with aircraft and tower measurements of CO_2. Adopting SIF, instead of EVI, for modeling the seasonal cycle of tundra photosynthesis can result in more accurate estimates of growing season duration and net carbon uptake by arctic vegetation.

A multiyear estimate of methane fluxes in Alaska from CARVE atmospheric observations

Methane (CH4) fluxes from Alaska and other arctic regions may be sensitive to thawing permafrost and future climate change, but estimates of both current and future fluxes from the region are uncertain. This study estimates CH4 fluxes across Alaska for 2012-2014 using aircraft observations from the Carbon in Arctic Reservoirs Vulnerability Experiment (CARVE) and a geostatistical inverse model (GIM). We find that a simple flux model based on a daily soil temperature map and a static map of wetland extent reproduces the atmospheric CH4 observations at the state-wide, multi-year scale more effectively than global-scale, state-of-the-art process-based models. This result points to a simple and effective way of representing CH4 flux patterns across Alaska. It further suggests that contemporary process-based models can improve their representation of key processes that control fluxes at regional scales, and that more complex processes included in these models cannot be evaluated given the information content of available atmospheric CH4 observations. In addition, we find that CH4 emissions from the North Slope of Alaska account for 24% of the total statewide flux of 1.74 ± 0.44 Tg CH4 (for May-Oct.). Contemporary global-scale process models only attribute an average of 3% of the total flux to this region. This mismatch occurs for two reasons: process models likely underestimate wetland area in regions without visible surface water, and these models prematurely shut down CH4 fluxes at soil temperatures near 0°C. As a consequence, wetlands covered by vegetation and wetlands with persistently cold soils could be larger contributors to natural CH4 fluxes than in process estimates. Lastly, we find that the seasonality of CH4 fluxes varied during 2012-2014, but that total emissions did not differ significantly among years, despite substantial differences in soil temperature and precipitation; year-to-year variability in these environmental conditions did not affect obvious changes in total CH4 fluxes from the state.

Detecting regional patterns of changing CO2 flux in Alaska

Significance Dramatic warming in northern high latitudes has led to increased photosynthetic carbon uptake during the short, intense growing season; however, microbial decomposition of soil carbon and increased emissions during the long cold season may offset summer uptake and impart a positive feedback on the global climate system. We show that current airborne and satellite measurements of atmospheric CO2 can accurately quantify summer uptake but are insufficient to detect regional changes in cold season emissions. As the potential for Arctic carbon budgets to become impacted by permafrost thaw and cold season emissions increases, strategies focused on year-round vertical profiles and improved spatial sampling will be needed to track carbon balance changes. With rapid changes in climate and the seasonal amplitude of carbon dioxide (CO2) in the Arctic, it is critical that we detect and quantify the underlying processes controlling the changing amplitude of CO2 to better predict carbon cycle feedbacks in the Arctic climate system. We use satellite and airborne observations of atmospheric CO2 with climatically forced CO2 flux simulations to assess the detectability of Alaskan carbon cycle signals as future warming evolves. We find that current satellite remote sensing technologies can detect changing uptake accurately during the growing season but lack sufficient cold season coverage and near-surface sensitivity to constrain annual carbon balance changes at regional scale. Airborne strategies that target regular vertical profile measurements within continental interiors are more sensitive to regional flux deeper into the cold season but currently lack sufficient spatial coverage throughout the entire cold season. Thus, the current CO2 observing network is unlikely to detect potentially large CO2 sources associated with deep permafrost thaw and cold season respiration expected over the next 50 y. Although continuity of current observations is vital, strategies and technologies focused on cold season measurements (active remote sensing, aircraft, and tall towers) and systematic sampling of vertical profiles across continental interiors over the full annual cycle are required to detect the onset of carbon release from thawing permafrost.

Plant Uptake of Atmospheric Carbonyl Sulfide in Coast Redwood Forests

Author(s): Campbell, JE; Whelan, ME; Berry, JA; Hilton, TW; Zumkehr, A; Stinecipher, J; Lu, Y; Kornfeld, A; Seibt, U; Dawson, TE; Montzka, SA; Baker, IT; Kulkarni, S; Wang, Y; Herndon, SC; Zahniser, MS; Commane, R; Loik, ME | Abstract: ©2017. American Geophysical Union. All Rights Reserved. The future resilience of coast redwoods (Sequoia sempervirens) is now of critical concern due to the detection of a 33% decline in California coastal fog over the 20th century. However, ecosystem-scale measurements of photosynthesis and stomatal conductance are challenging in coast redwood forests, making it difficult to anticipate the impacts of future changes in fog. To address this methodological problem, we explore coastal variations in atmospheric carbonyl sulfide (COS or OCS), which could potentially be used as a tracer of these ecosystem processes. We conducted atmospheric flask campaigns in coast redwood sites, sampling at surface heights and in the canopy (~70 m), at the University of California Landels-Hill Big Creek Reserve and Big Basin State Park. We simulated COS atmosphere-biosphere exchange with a high-resolution 3-D model to interpret these data. Flask measurements indicated a persistent daytime drawdown between the coast and the downwind forest (45 ± 6 ppt COS) that is consistent with the expected relationship between COS plant uptake, stomatal conductance, and gross primary production. Other sources and sinks of COS that could introduce noise to the COS tracer technique (soils, anthropogenic activity, nocturnal plant uptake, and surface hydrolysis on leaves) are likely to be small relative to daytime COS plant uptake. These results suggest that COS measurements may be useful for making ecosystem-scale estimates of carbon, water, and energy exchange in coast redwood forests.

The influence of daily meteorology on boreal fire emissions and regional trace gas variability

Author(s): Wiggins, EB; Veraverbeke, S; Henderson, JM; Karion, A; Miller, JB; Lindaas, J; Commane, R; Sweeney, C; Luus, KA; Tosca, MG; Dinardo, SJ; Wofsy, S; Miller, CE; Randerson, JT | Abstract: ©2016. American Geophysical Union. All Rights Reserved. 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.