the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Characterization of trace gas emissions from controlled laboratory burning of Canadian boreal forest fuels
Abstract. Although boreal wildfires are a major global source of trace gases, their emissions remain poorly characterized. To address this gap, controlled burns of Canadian Boreal surface and ground fuels were conducted during the Biomass Burning Canada (BBCan) Campaign. Emission factors (EF) for 46 volatile organic compounds (VOC) were determined using iodide chemical ionization mass spectrometry (I-CIMS) and Vocus proton transfer reaction mass spectrometry (Vocus PTR-MS). Total non-methane organic compound (NMOC) emissions, which were measured separately, were found to account for 1–13 % of total emitted gas-phase carbon (i.e., CO2, CO, CH4, NMOC), with total quantified VOCs (ΣVOCs) accounting for 13–34 % of that fraction. The dominant compounds contributing to the measured ΣVOCs include oxygenates and organic reactive nitrogen (Nr) species. Boreal peat fuels, which are prone to residual smoldering combustion, produced significantly higher total NMOC, total Nr, and individual VOC emissions than the other fuels. In contrast, boreal mulch, which burned very efficiently, produced low emissions. Combustion efficiency was observed to have a strong impact on total and individual VOC emissions, but VOC emission profiles were also dependent on fuel type and moisture content. The findings indicate that the EFs currently used to speciate NMOC emission may not adequately capture emissions from smoldering boreal peat fires. Study results provide the first comprehensive VOC EF for fresh emissions for a range of Canadian boreal surface and ground fuels, which can be used to improve emission inventories and enhance predictions of wildfire smoke impacts on air quality, climate, and health.
Competing interests: At least one of the (co-)authors is a member of the editorial board of Atmospheric Chemistry and Physics.
Publisher's note: Copernicus Publications remains neutral with regard to jurisdictional claims made in the text, published maps, institutional affiliations, or any other geographical representation in this paper. While Copernicus Publications makes every effort to include appropriate place names, the final responsibility lies with the authors. Views expressed in the text are those of the authors and do not necessarily reflect the views of the publisher.- Preprint
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Data sets
Replication data for: Emission factors for gaseous species measured at the individual burn level using I-CIMS and Vocus PTR-MS Rowshon Afroz https://doi.org/10.5683/SP3/OGR3J1
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In this manuscript, Afroz et al. fill the gap in the current understanding of Canadian wildfire boreal surface fuels and provide useful implications for evaluating current Canadian wildfire emission inventories, which underestimate the Canadian boreal peat EF. This manuscript also takes advantage of two Picarro measurements to quantify the total NMOC and provides promising insight by using fuel moisture to explain the variability in VOC emissions. However, several aspects require further clarification. In particular, the manuscript needs better justification for the duct-flow-based EF calculation method relative to the more commonly used carbon mass balance approach, and for missing low-molecular-weight VOCs and gas-particle partitioning. In addition, some comparisons between laboratory and aircraft-based measurements would benefit from a more cautious interpretation that accounts for differences in fuel type, combustion conditions, plume age, dilution, chemical processing, and sampling platform.
My major comments are below:
Detailed comments are:
Line 319, acrylic acid should be C₃H₄O₂.
Line 330-334, guaiacol is considered a low-temperature pyrolysis indicator in a PMF analysis. Even high- or low-temperature pyrolysis does not correspond exactly to the commonly used “flaming” or “smoldering”, but it still can be helpful to add here.
Line 372, can you explain why MU has poor correlations?
Line 391, most of the quantified VOC. How many? Can you present XX out of 46 or as a percentage?
Line 560, the higher EFs of HONO, NO, VOCs, and other species observed in lab studies compared with aircraft measurements cannot be explained simply by the difference between fresh and aged smoke. Other factors, such as differences in fuel type, peat contribution, fuel nitrogen content, combustion conditions, and sampling platform, can also affect this. For example, peat fuels can emit more N-containing species, while aircraft measurements of aged plumes may be affected by chemical processing, gas-particle partitioning, dilution, and possible loss or evaporation of SVOCs, IVOCs, etc.
Citation:
https://pubs.acs.org/doi/abs/10.1021/acs.est.3c05017
www.atmos-chem-phys.net/14/199/2014/
10.5194/acp-11-12197-2011
https://doi.org/10.1002/jgrd.50828