We present a decadal (1994-2004) record of carbon dioxide flux in a 160-year-old black spruce forest/veneer bog complex in central Manitoba, Canada. The ecosystem shifted from a source (+41 g Cm-2, 1995) to a sink (-21 g C m-2, 2004) of CO2 over the decade, with an average net carbon balance near zero. Annual mean temperatures increased 1-2° during the period, consistent with the decadal trend across the North American boreal biome. We found that ecosystem carbon exchange responded strongly to air temperature, moisture status, potential evapotranspiration, and summertime solar radiation. The seasonal cycle of ecosystem respiration significantly lagged that of photosynthesis, limited by the rate of soil thaw and the slow drainage of the soil column. Factors acting over long time scales, especially water table depth, strongly influenced the carbon budget on annual time scales. Net uptake was enhanced and respiration inhibited by multiple years of rainfall in excess of evaporative demand. Contrary to expectations, we observed no correlation between longer growing seasons and net uptake, possibly because of offsetting increases in ecosystem respiration. The results indicate that the interactions between soil thaw and water table depth provide critical controls on carbon exchange in boreal forests underlain by peat, on seasonal to decadal time scales, and these factors must be simulated in terrestrial biosphere models to predict response of these regions to future climate. © 2007 Blackwell Publishing Ltd.

We used eddy covariance to measure the net exchange of CO₂ between the atmosphere and a black spruce (Picea mariana) forest in Manitoba for 16,500 hours from March 16, 1994 to October 31, 1996. We then partitioned net exchange into gross photosynthesis and respiration by estimating daytime respiration as a function of temperature, and used these data to define the physiological responses of the forest to weather. The annual rates of gross production and respiration by the forest were both around 8 t C ha⁻¹ yr⁻¹. Both photosynthetic and respiratory response were reduced in winter, recovered with warming in spring, and varied little in summer. Respiration in mid summer increased with air temperature (T _air) at a Q ₁₀ of around 2 to a rate of 2–8 μmol m⁻² s⁻¹ at 15°C. Gross photosynthesis at high light (photon flux density (PPFD) greater than 600 μmol m⁻² s⁻¹) was negligible at T_air < 0°C, increased linearly with T_air from 0° to 14°C, and was relatively insensitive to T _air > 14°C. Gross CO₂ uptake at T _air > 14°C increased with increasing light at an ecosystem-level quantum yield of 0.05 mol CO₂ mol⁻¹ photons before saturating at an uptake rate of 8–18 μmol m⁻² s⁻¹ at PPFDs greater than 500–700 μmol m⁻² s⁻¹. Photosynthesis in summer did not appear limited by high evaporative demand or soil water depletion.

The first phase of the Atmospheric Tomography Mission (ATom-1) took place in July-August 2016 and included flights above the remote Pacific and Atlantic oceans. Sampling of atmospheric constituents during these flights is designed to provide new insights into the chemical reactivity and processes of the remote atmosphere and how these processes are affected by anthropogenic emissions. Model simulations provide a valuable tool for interpreting these measurements and understanding the origin of the observed trace gases and aerosols, so it is important to quantify model performance. Goddard Earth Observing System Model version 5 (GEOS-5) forecasts and analyses show considerable skill in predicting and simulating the CO distribution and the timing of CO enhancements observed during the ATom-1 aircraft mission. We use GEOS-5's tagged tracers for CO to assess the contribution of different emission sources to the regions sampled by ATom-1 to elucidate the dominant anthropogenic influences on different parts of the remote atmosphere. We find a dominant contribution from non-biomass-burning sources along the ATom transects except over the tropical Atlantic, where African biomass burning makes a large contribution to the CO concentration. One of the goals of ATom is to provide a chemical climatology over the oceans, so it is important to consider whether August 2016 was representative of typical boreal summer conditions. Using satellite observations of 700 hPa and column CO from the Measurement of Pollution in the Troposphere (MOPITT) instrument, 215 hPa CO from the Microwave Limb Sounder (MLS), and aerosol optical thickness from the Moderate Resolution Imaging Spectroradiometer (MODIS), we find that CO concentrations and aerosol optical thickness in August 2016 were within the observed range of the satellite observations but below the decadal median for many of the regions sampled. This suggests that the ATom-1 measurements may represent relatively clean but not exceptional conditions for lower-tropospheric CO.

Formic acid (HCOOH) is an important component of atmospheric acidity but its budget is poorly understood, with prior observations implying substantial missing sources. Here we combine pole-to-pole airborne observations from the Atmospheric Tomography Mission (ATom) with chemical transport model (GEOS-Chem CTM) and back trajectory analyses to provide the first global in-situ characterization of HCOOH in the remote atmosphere. ATom reveals sub-100 ppt HCOOH concentrations over most of the remote oceans, punctuated by large enhancements associated with continental outflow. Enhancements correlate with known combustion tracers and trajectory-based fire influences. The GEOS-Chem model underpredicts these in-plume HCOOH enhancements, but elsewhere we find no broad indication of a missing HCOOH source in the background free troposphere. We conclude that missing non-fire HCOOH precursors inferred previously are predominantly short-lived. We find indications of a wet scavenging underestimate in the model consistent with a positive HCOOH bias in the tropical upper troposphere. Observations reveal episodic evidence of ocean HCOOH uptake, which is well-captured by GEOS-Chem; however, despite its strong seawater undersaturation HCOOH is not consistently depleted in the remote marine boundary layer. Over fifty fire and mixed plumes were intercepted during ATom with widely varying transit times and source regions. HCOOH:CO normalized excess mixing ratios in these plumes range from 3.4 to >50 ppt/ppb CO and are often over an order of magnitude higher than expected primary emission ratios. HCOOH is thus a major reactive organic carbon reservoir in the aged plumes sampled during ATom, implying important missing pathways for in-plume HCOOH production.

In Amazon forests, the relative contributions of climate, phenology, and disturbance to net ecosystem exchange of carbon (NEE) are not well understood. To partition influences across various timescales, we use a statistical model to represent eddy-covariance-derived NEE in an evergreen eastern Amazon forest as a constant response to changing meteorology and phenology throughout a decade. Our best fit model represented hourly NEE variations as changes due to sunlight, while seasonal variations arose from phenology influencing photosynthesis and from rainfall influencing ecosystem respiration, where phenology was asynchronous with dry-season onset. We compared annual model residuals with biometric forest surveys to estimate impacts of drought disturbance. We found that our simple model represented hourly and monthly variations in NEE well (R 2 Combining double low line 0.81 and 0.59, respectively). Modeled phenology explained 1 % of hourly and 26 % of monthly variations in observed NEE, whereas the remaining modeled variability was due to changes in meteorology. We did not find evidence to support the common assumption that the forest phenology was seasonally light- or water-triggered. Our model simulated annual NEE well, with the exception of 2002, the first year of our data record, which contained 1.2 MgC ha'1 of residual net emissions, because photosynthesis was anomalously low. Because a severe drought occurred in 1998, we hypothesized that this drought caused a persistent, multi-year depression of photosynthesis. Our results suggest drought can have lasting impacts on photosynthesis, possibly via partial damage to still-living trees.

The MethaneSAT satellite instrument and its aircraft precursor, MethaneAIR, are imaging spectrometers designed to measure methane concentrations with wide spatial coverage, fine spatial resolution, and high precision compared to currently deployed remote sensing instruments. At 12 960 m cruise altitude above ground (13 850 m above sea level), MethaneAIR datasets have a 4.5 km swath gridded to 10 m × 10 m pixels with 17-20 ppb standard deviation on a flat scene. MethaneAIR was deployed in the summer of 2021 in the Permian Basin to test the accuracy of the retrieved methane concentrations and emission rates using the algorithms developed for MethaneSAT. We report here point source emissions obtained during a single-blind volume-controlled release experiment, using two methods. (1) The modified integrated mass enhancement (mIME) method estimates emission rates using the total mass enhancement of methane in an observed plume combined with winds obtained from Weather Research Forecast driven by High-Resolution Rapid Refresh meteorological data in Large Eddy Simulations mode (WRF-LES-HRRR). WRF-LES-HRRR simulates winds in stochastic eddy-scale (100-1000 m) variability, which is particularly important for low-wind conditions and informing the error budget. The mIME can estimate emission rates of plumes of any size that are detectable by MethaneAIR. (2) The divergence integral (DI) method applies Gauss's theorem to estimate the flux divergence fields through a series of closed surfaces enclosing the sources. The set of boxes grows from the upwind side of the plume through the core of each plume and downwind. No selection of inflow concentration, as used in the mIME, is required. The DI approach can efï¬ ciently determine ï¬ uxes from large sources and clusters of sources but cannot resolve small point emissions. These methods account for the effects of eddy-scale variation in different ways: The DI averages across many eddies, whereas the mIME re-samples many eddies from the LES simulation. The DI directly uses HRRR winds, while mIME uses WRF-LES-HRRR wind products. Emissions estimates from both the mIME and DI methods agreed closely with the single-blind volume-controlled experiments (N Combining double low line 21). The York regression between the estimated emissions and the released emissions has a slope of 0.96 [0.84, 1.08], R Combining double low line 0.83 and N Combining double low line 21, with 30 % mean percentage error for the whole dataset, which indicates that MethaneAIR can quantify point sources emitting more than 200 kg h-1 for the mIME and 500 kg h-1 for the DI method. The two methods also agreed on methane emission estimates from various uncontrolled sources in the Permian Basin. The experiment thus demonstrates the powerful potential of the MethaneAIR instrument and suggests that the quantification method should be transferable to MethaneSAT if it meets the design specifications.

The net ecosystem exchange of carbon dioxide was measured by eddy covariance methods for 3 years in two old-growth forest sites near Santarém, Brazil. Carbon was lost in the wet season and gained in the dry season, which was opposite to the seasonal cycles of both tree growth and model predictions. The 3-year average carbon loss was 1.3 (confidence interval: 0.0 to 2.0) megagrams of carbon per hectare per year. Biometric observations confirmed the net loss but imply that it is a transient effect of recent disturbance superimposed on long-term balance. Given that episodic disturbances are characteristic of old-growth forests, it is likely that carbon sequestration is lower than has been inferred from recent eddy covariance studies at undisturbed sites.                      

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.