Contribution Of Biomass Burning Emissions Research Articles

Significant chlorine emissions from biomass burning affect the long-term atmospheric chemistry in Asia.

Biomass burning (BB) is a major source of trace gases and particles in the atmosphere, influencing air quality, radiative balance, and climate. Previous studies have mainly focused on the BB emissions of carbon and nitrogen species with less attention on chlorine. Reactive chlorine chemistry has significant effects on atmospheric chemistry and air quality. However, quantitative information on chlorine emissions from BB, particularly the long-term trend and associated atmospheric impacts, is limited both on regional and global scales. Here, we report a long-term (2001-2018) high-resolution BB emission inventory for the major chlorine-containing compounds (HCl, chloride, and CH3Cl) in Asia based on satellite observations. We estimate an average of 730 Gg yr-1 chlorine emitted from BB activity in Asia, with China contributing the largest share at 24.2% (177 Gg yr-1), followed by Myanmar at 18.7% and India at 18.3%. Distinct seasonal patterns and significant spatial and interannual variability are observed, mainly driven by human-mediated changes in agricultural activity. By incorporating the newly developed chlorine emission inventory into a global chemistry-climate model (CAM-Chem), we find that the BB-chlorine emissions lead to elevated levels of HCl and CH3Cl (monthly average up to 2062 and 1421 parts per trillion by volume (pptv), respectively), subsequently resulting in noticeable changes in oxidants (up to 3.1% in O3 and 17% in OH radicals). The results demonstrate that BB is not only a significant source of air pollutants but also of oxidants, suggesting a larger role of BB emissions in the atmospheric chemistry and oxidation process than previously appreciated. In light of the projected increase in BB activity toward the end of the century and the extensive control of anthropogenic emissions worldwide, the contribution of BB emissions may become fundamental to air quality composition in the future.

Molecular compositions of marine organic aerosols over the Bohai and Yellow Seas: Influence of primary emission and secondary formation

To understand the influences of continental emissions on marine aerosols from East Asia, the total suspended particle (TSP) samples were collected from the Yellow Sea (YS) and Bohai Sea (BS) of China through a cruise campaign during the spring of 2018. >100 individual organic compounds were identified and determined in the samples, and they were classified into 6 major groups according to the functionality and sources. The mass concentrations of total quantified organic compounds in BS (307.6 ± 268.3 ng m−3) was approximately 3 times those of YS (111.0 ± 97.3 ng m−3). Organic compounds from biomass burning (23.2 ± 34.2 ng m−3), marine/microbial source (23.1 ± 6.2 ng m−3) and fossil fuel combustion (21.4 ± 11.3 ng m−3) were the most abundant in the YS samples, whereas primary biological origins (90.0 ± 107.1 ng m−3), biomass burning (52.1 ± 39.1 ng m−3) and fossil fuel combustion (41.9 ± 20.1 ng m−3) were the most important organic species in BS marine aerosols. The concentrations of total biogenic secondary organic aerosol (BSOA) tracers including six isoprene SOA (SOAI), three monoterpene SOA (SOAM), and one β-caryophyllene SOA (SOAC) were 2.4 ± 1.5 ng m−3 and 7.3 ± 4.4 ng m−3 in the YS and BS samples, respectively. A strong correlation between BSOA tracers and levoglucosan was shown in the marine aerosol samples, indicating that biomass burning emissions could also promote BSOA formations. The spatial distribution of chemical and source characteristics suggests a relatively large impacts of continental emissions to the BS aerosols. Based on the tracer-based method, the biomass burning (YS: 4.9 ± 6.8%; BS: 8.8 ± 8.0%) was the largest contributor to OC, followed by primary biogenic OC (YS: 0.59 ± 0.44%; BS: 2.9 ± 3.0%) and biogenic secondary OC (YS: 0.45 ± 0.23%; BS: 1.0 ± 0.59%). This study suggests important contributions of biomass burning emissions to organic aerosols in the YS and BS marine atmosphere, although marine source, fossil fuel combustion and secondary formation was also substantial.

Striking impacts of biomass burning on PM2.5 concentrations in Northeast China through the emission inventory improvement

Biomass burning exerts substantial influences on air quality and climate, which in turn to further aggravate air quality. The biomass burning emissions in particular of the agricultural burning may suffer large uncertainties which limits the understanding of their impact on air quality. Based on an improved emission inventory of the Visible Infrared Imaging Radiometer Suite (VIIRS) relative to commonly used Global Fire Emissions Database (GFED), we thoroughly evaluate the impact of biomass burning on air quality and climate during the episodes of November 2017 in Northeast China which is rich in agriculture burning. The results first indicate substantial underestimates in simulated PM2.5 concentrations without the inclusion of biomass burning emission inventory, based on a regional air quality model Weather Research and Forecasting model and Community Multiscale Air Quality model (WRF-CMAQ). The addition of biomass burning emissions from GFED then reduces the bias to a certain extent, which is further reduced by replacing the agricultural fires data in GFED with VIIRS. Numerical sensitivity experiments show that based on the improved emission inventory, the contribution of biomass burning emissions to PM2.5 concentrations in Northeast China reaches 32%, contrasting to 15% based on GFED, during the episode from November 1 to 7, 2017. Aerosol direct radiative effects from biomass burning are finally elucidated, which not only reduce downward surface shortwave radiation and planetary boundary layer height, but also affect the vertical distribution of air temperature, wind speed and relative humidity, favorable to the accumulation of PM2.5. During November 1–7, 2017, the mean daily PM2.5 enhancement due to aerosol radiative effects from VIIRS_G is 16 μg m−3, a few times higher than that of 2.8 μg m−3 from GFED. The study stresses the critical role of biomass burning, particularly of small fires easily missed in the traditional low-resolution satellite products, on air quality.

Combustion related ammonia promotes PM2.5 accumulation in autumn in Tianjin, China

Ammonium (NH4+) is one of the most important inorganic components in PM2.5, and plays key roles in increasing the concentration of PM2.5. Understanding the sources and formation processes of NH4+ is an effective way to control PM2.5. In this study, daily PM2.5 samples were collected from September 01 to November 30, 2017 in Tianjin, and water-soluble ion concentrations and δ15N-NH4+ in PM2.5 were analyzed. The results showed that (NH4)2SO4 and NH4NO3 were the major chemical forms of NH4+. In particular, NH4NO3 dominated the liquid water content (ALWC) increase on haze days, leading to more NH3 partitioning into the particle phase, and this formation mechanism of NH4NO3 might be self-amplified with an increase in ALWC concentrations. The mean values of δ15N-NH4+ were 14.7 ± 5.2‰, and the estimated initial ambient δ15N-NH3 was −15.6 ± 9.3‰. The mean fractional contributions of volatilization sources, fossil fuel-related sources and biomass burning were 31.9 ± 15.8%, 45.9 ± 12.6% and 22.2 ± 18.3%, respectively, which were estimated by the stable isotope mixing model. Obviously, the NH3 related to combustion emissions (68.1 ± 15.9%) dominated the source of aerosol NH4+ during autumn in Tianjin in this study. We also found that the fractional contributions of these sources have varied during different pollution periods, and the contributions of biomass burning emissions increased to 60% on haze days in November. Our results highlight that fossil fuel related source emissions of NH3 dominate the formation of NH4NO3 in autumn, leading to the occurrence of haze in autumn in Tianjin. Nevertheless, the biomass burning emissions were non-ignorable.

Analysis of the Contribution of Biomass Burning Emissions in East Asia to the PM<sub>10</sub> and Radiation Energy Budget in Korea

Analysis of the Contribution of Biomass Burning Emissions in East Asia to the PM<sub>10</sub> and Radiation Energy Budget in Korea

Attributed radiative forcing of air pollutants from biomass and fossil burning emissions

Energy is vital to human society but significantly contributes to the deterioration of environmental quality and the global issue of climate change. Biomass and fossil fuels are important energy sources but have distinct pollutant emission characteristics during the burning process. This study aimed at attributing radiative forcing of climate forcers, including greenhouse gases but also short-lived climate pollutants, from the burning of fossil and biomass fuels, and the spatiotemporal characteristics. We found that air pollutant emissions from the burning process of biofuel and fossil fuels induced RFs of 68.2 ± 36.8 mW m−2 and 840 ± 225 mW m−2, respectively. The relatively contribution of biomass burning emissions was 7.6% of that from both fossil and biofuel combustion processes, while its contribution in energy supply was 11%. These relative contributions varied obviously across different regions. The per unit energy consumption of biomass fuel in the developed regions, such as North America (0.57 ± 0.33 mW m−2/107TJ) and Western Europe (0.98 ± 0.79 mW m−2/107TJ), had higher impacts of combustion emission related RFs compared to that of developing regions, like China (0.40 ± 0.26 mW m−2/107TJ), and South and South-East Asia (0.31 ± 0.71 mW m−2/107TJ) where low efficiency biomass burning in residential sector produced significant amounts of organic matter that had a cooling effect. Note that the study only evaluated fuel combustion emission related RFs, and those associated with the production of fuels and land use change should be studied later in promoting a comprehensive understanding on the climate impacts of biomass utilization.

Large contribution of biomass burning emissions to ozone throughout the global remote troposphere

Ozone is the third most important anthropogenic greenhouse gas after carbon dioxide and methane but has a larger uncertainty in its radiative forcing, in part because of uncertainty in the source characteristics of ozone precursors, nitrogen oxides, and volatile organic carbon that directly affect ozone formation chemistry. Tropospheric ozone also negatively affects human and ecosystem health. Biomass burning (BB) and urban emissions are significant but uncertain sources of ozone precursors. Here, we report global-scale, in situ airborne measurements of ozone and precursor source tracers from the NASA Atmospheric Tomography mission. Measurements from the remote troposphere showed that tropospheric ozone is regularly enhanced above background in polluted air masses in all regions of the globe. Ozone enhancements in air with high BB and urban emission tracers (2.1 to 23.8 ppbv [parts per billion by volume]) were generally similar to those in BB-influenced air (2.2 to 21.0 ppbv) but larger than those in urban-influenced air (-7.7 to 6.9 ppbv). Ozone attributed to BB was 2 to 10 times higher than that from urban sources in the Southern Hemisphere and the tropical Atlantic and roughly equal to that from urban sources in the Northern Hemisphere and the tropical Pacific. Three independent global chemical transport models systematically underpredict the observed influence of BB on tropospheric ozone. Potential reasons include uncertainties in modeled BB injection heights and emission inventories, export efficiency of BB emissions to the free troposphere, and chemical mechanisms of ozone production in smoke. Accurately accounting for intermittent but large and widespread BB emissions is required to understand the global tropospheric ozone burden.

Temporal variations in the chemical composition of aerosols over the coastal Bay of Bengal

Variations in source, ionic composition and carbonaceous components of aerosols are expected in the atmosphere due to reversing the direction of winds from winter to summer over the coastal Bay of Bengal (BoB). To examine this monthly, samples were collected at the weekly interval between March 2016 and February 2017 in the coastal BoB. The air mass back trajectories suggested that the study region received aerosols from Indo-Gangetic Plain from October to February whereas from central India during June to September and south or southwest during March to May. A higher concentration of total suspended particulate matter (TSP) was observed from November to February (winter) compared to other months. The concentration of sulphate contributed more than half of water-soluble inorganic species followed by sodium, ammonium and nitrate. The dominant contribution of anthropogenic SO42− (>90%) to total SO42− was observed. The ambient elemental carbon loadings and organic carbon to EC ratios indicate the dominant contribution of biomass burning emissions in the study region. The significant contribution of non-sea salt sulphate and nss-K+ indicates a dominant contribution from the continental sources throughout the year. The mass ratio of NO3−/anthropogenic SO42− suggests stationary sources (i.e., coal burning in power plants) contribute significantly over vehicular emissions during the entire study period. The mass balance of ionic composition suggests the acidic nature of aerosols. The estimated secondary aerosols accounted for ∼50% of organic carbon and 7% of TSP in the study region. This study has implications for understanding the source, composition and nature of aerosols and possible impacts on coastal water upon its deposition.

Chemical composition and bioreactivity of PM2.5 during 2013 haze events in China

Abstract Chemical composition and bioreactivity of PM2.5 samples collected from Beijing (BJ), Xi'an (XA), Xiamen (XM) and Hong Kong (HK) in China during haze events were characterized. PM2.5 mass concentrations in BJ, XA, XM and HK in the episodes were found to be 258 ± 100 μg m−3, 233 ± 52 μg m−3, 46 ± 9 μg m−3 and 48 ± 13 μg m−3, respectively. Significant increase of sulfate, nitrate and ammonium concentrations in northern cities were observed. High contributions of biomass burning emissions to organic carbon (OC) in northern cities were estimated in this study implying frequent biomass burning during the haze periods. The urea concentrations in PM2.5 were 1855 ± 755 ng m−3 (BJ), 1124 ± 243 ng m−3 (XA), 543 ± 104 ng m−3 (XM) and 363 ± 61 ng m−3 (HK) suggesting higher or close to upper limits compared to other regions in the world. Dose-dependent alterations in oxidative potential, IL-6, IFN-γ and TNF-α levels were also investigated. The oxidative potential levels are BJ > XM > XA > HK, whereas levels of IL-6, IFN-γ and TNF-α were BJ > XA > XM > HK. The sulfate, nitrate, ammonium, OC, urea and levoglucosan are associated with oxidative-inflammatory responses. These experimental results are crucial for the policymakers to implement cost-effective abatement strategies for improving air quality.

Characteristics and applications of size-segregated biomass burning tracers in China's Pearl River Delta region

Biomass burning activities in China are ubiquitous and the resulting smoke emissions may pose considerable threats to human health and the environment. In the present study, size-segregated biomass burning tracers, including anhydrosugars (levoglucosan (LG) and mannosan (MN)) and non-sea-salt potassium (nss-K+), were determined at an urban and a suburban site in the Pearl River Delta (PRD) region. The size distributions of biomass burning tracers were generally characterized by a unimodal pattern peaking in the particle size range of 0.44–1.0 μm, except for MN during the wet season, for which a bimodal pattern (one in fine and one in coarse mode) was observed. These observed biomass burning tracers in the PRD region shifted towards larger particle sizes compared to the typical size distributions of fresh biomass smoke particles. Elevated biomass burning tracers were observed during the dry season when biomass burning activities were intensive and meteorological conditions favored the transport of biomass smoke particles from the rural areas in the PRD and neighboring areas to the sampling sites. The fine mode biomass burning tracers significantly correlated with each other, confirming their common sources. Rather high ΔLG/ΔMN ratios were observed at both sites, indicating limited influence from softwood combustion. High Δnss-K+/ΔLG ratios further suggested that biomass burning aerosols in the PRD were predominately associated with burning of crop residues. Using a simplified receptor-oriented approach with an emission factor of 0.075 (LG/TC) obtained from several chamber studies, average contributions of biomass burning emissions to total carbon in fine particles were estimated to be 23% and 16% at the urban and suburban site, respectively, during the dry season. In contrast, the relative contributions to total carbon were lower than 8% at both sites during the wet season.

Seasonal variations of anhydrosugars in PM2.5 in the Pearl River Delta Region, China

Anhydrosugars including levoglucosan and mannosan are the most effective organic tracers for biomass burning aerosol in the atmosphere. In this study, to investigate the contribution of biomass burning emissions to the aerosol burden in the Pearl River Delta (PRD) region, China, 24-hour integrated PM2.5 samples were collected simultaneously at four locations, (i) Guangzhou (GZ), (ii) Zhaoqing (ZQ) in Guangdong province, (iii) Hok Tsui (HT) and (iv) Hong Kong Polytechnic University (PU) in Hong Kong, in four seasons between 2006 and 2007. Levoglucosan and mannosan, together with water-soluble inorganic ions and water-soluble organic carbon (WSOC), were determined to elucidate the seasonal and spatial variations in biomass burning contributions. The concentrations of levoglucosan and mannosan were on average 82.4±123 and 5.8±8.6 ng m−3, respectively. The WSOC concentrations ranged from 0.2 to 9.4 µg m−3, with an average of 2.1±1.6 µg m−3. The relative contributions of biomass burning emissions to OC were 33% in QZ, 12% in GZ, 4% at PU and 5% at HT, respectively, estimated by the measured levoglucosan to organic carbon ratio (LG/OC) relative to literature-derived LG/OC values. The contributions from biomass burning emissions were in general 1.7–2.8 times higher in winter than those in other seasons. Further, it was inferred from diagnostic tracer ratios that a significant fraction of biomass burning emissions was derived from burning of hard wood and likely also from field burning of agricultural residues, such as rice straw, in the PRD region. Our results highlight the contributions from biomass/biofuel burning activities on the regional aerosol budget in South China.

Ozone production from the interaction of wildfire and biogenic emissions: a case study in Russia during spring 2006

Abstract. The objective of this study is to investigate the contribution of biomass burning emissions to O3 production during small-scale dry-grass fires over Western Russia (24 April–10 May 2006) as well as to quantify the effect of biogenic emissions in this environment. By using the Factor Separation methodology, we evaluate the pure contribution of each one of these two sources and we appoint the significance of their synergistic effect on O3 production. The total (actual) contribution of each source is also estimated. Sensitivity simulations assess the effect of various fire emission parameters, such as chemical composition, emissions magnitude and injection height. The model results are compared with O3 and isoprene observations from 117 and 9 stations of the EMEP network, respectively. Model computations show that the fire episode determines the sensitivity of O3 chemistry in the area. The reference run which represents grass fires with high NOx/CO emission ratio (0.06) is characterized by VOC-sensitive O3 production. In that case, the pure impact of fire emissions on surface O3 is up to 40–45 ppb, while their synergistic effect with the biogenic emissions is proven significant (up to 8 ppb). Under a lower NOx/CO molar ratio (0.025, representative of agricultural residues), the area is characterized by NOx-sensitive chemistry and the maximum surface O3 predictions are almost doubled due to higher O3 production at the fire spots and lower fires' NO emissions.

Biomass burning contributions to urban aerosols in a coastal Mediterranean City

Mean annual biomass burning contributions to the bulk particulate matter (PMX) load were quantified in a southern-European urban environment (Barcelona, Spain) with special attention to typical Mediterranean winter and summer conditions. In spite of the complexity of the local air pollution cocktail and the expected low contribution of biomass burning emissions to PM levels in Southern Europe, the impact of these emissions was detected at an urban background site by means of tracers such as levoglucosan, K+ and organic carbon (OC). The significant correlation between levoglucosan and OC (r2=0.77) and K+ (r2=0.65), as well as a marked day/night variability of the levoglucosan levels and levoglucosan/OC ratios was indicative of the contribution from regional scale biomass burning emissions during night-time transported by land breezes. In addition, on specific days (21–22 March), the contribution from long-range transported biomass burning aerosols was detected.Quantification of the contribution of biomass burning aerosols to PM levels on an annual basis was possible by means of the Multilinear Engine (ME). Biomass burning emissions accounted for 3% of PM10 and PM2.5 (annual mean), while this percentage increased up to 5% of PM1. During the winter period, regional-scale biomass burning emissions (agricultural waste burning) were estimated to contribute with 7±4% of PM2.5 aerosols during night-time (period when emissions were clearly detected). Long-range transported biomass burning aerosols (possibly from forest fires and/or agricultural waste burning) accounted for 5±2% of PM2.5 during specific episodes. Annually, biomass burning emissions accounted for 19%–21% of OC levels in PM10, PM2.5 and PM1. The contribution of this source to K+ ranged between 48% for PM10 and 97% for PM1 (annual mean). Results for K+ from biomass burning evidenced that this tracer is mostly emitted in the fine fraction, and thus coarse K+ could not be taken as an appropriate tracer of biomass burning.

Implications of fires on carbon budgets in Andean cloud montane forest: The importance of peat soils and tree resprouting

Fire in tropical montane cloud forests (TMCFs) is not as rare as once believed. Andean TMCFs sit immediately below highly flammable, high-altitude grasslands (Puna/Páramo) that suffer from recurrent anthropogenic fire. This treeline is a zone of climatic tension where substantial future warming is likely to force upward tree migrations, while increased fire presence and fire impacts are likely to force it downwards. TMCFs contain large carbon stocks in their peat soils and their loss through fire is a currently unaccounted for regional source of CO 2. This study, conducted in the southern Peruvian Andes (>2800 m), documents differences in live tree biomass, fine root biomass, fallen and standing dead wood, and soil organic carbon in 4 paired-sample plots (burned versus control) following the severe ground fires that occurred during the 2005 Andean drought. Peat soils contributed the most to biomass burning emissions, with lower values corresponding to an 89% mean stock difference compared to the controls (mean ± SE) (54.1 ± 22.3 vs. 5.8 ± 5.3 MgC ha −1). Contrastingly, carbon stocks from live standing trees differed by a non-significant 37% lower value in the burned plots compared to the controls, largely compensated by vigorous resprouting (45.5 ± 17.4 vs. 69.2 ± 13.4 MgC ha −1). Both standing dead trees and fallen dead wood were significantly higher in the burned plots with a three-fold difference from the controls: dead Trees 45.2 ± 9.4 vs. 16.4 ± 4.4 MgC ha −1, and ca. a 2 fold difference for the fallen dead wood: 11.2 ± 5 vs. 6.7 ± 3.2 MgC ha −1 for the burned plots versus their controls. A preliminary estimate of the regional contribution of biomass burning emissions from Andean TMCFs for the period 2000–2008, resulted in mean carbon emission rates of 1.3 TgC yr −1 (max-min: 1.8–0.8 TgC yr −1). This value is in the same order of magnitude than South American annual fire emissions (300 TgC yr −1) suggesting the need for further research on Andean forest fires. On-going projects on the region are working on the promotion of landowner participation in TMCFs conservation through REDD+ mechanism. The heart of the proposed initiative is reforestation of degraded lands with green fire breaks enriched with economically valuable Andean plant species. The cultivation of these species may contribute to reduce deforestation pressure on the Amazonian cloud forest by providing an alternative income to local communities, at the same time that they prevent the spread of fire into Manu National Park and adjacent community-held forests, protecting forest and reducing CO 2 emissions.

Relative contributions of biomass burning emissions and atmospheric transport to carbon monoxide interannual variability

Biomass burning is an important source of greenhouse gases and of ozone precursors such as CO. Recent analyses combining the use of satellite data and of ecosystem models showed that wild fire emissions are subject to a large interannual variability. In this study, NOAA/ESRL CO surface measurements are used in conjunction with the results from the LMDz‐INCA global chemistry‐transport model and analyzed over the 1997–2001 period in order to quantify the relative contributions of biomass burning emissions and of climate to the CO interannual variability (IAV). Over the considered five year period, the mean CO IAV was found to be about 11% for stations far from regional pollution and 4.5% for Antarctic stations. At both southern and northern high latitude stations, the CO IAV is controlled almost equally by variations in biomass burning emissions and atmospheric meteorology. On the contrary, meteorological variability prevails in the tropics, where it explains 50% to 90% of the CO IAV. Variability in long‐range transport and climate is thus the dominant process controlling the CO interannual variability, except during specific episodes, such as the intense fires associated with the 1997–1998 El Niño event.

Isotopic Composition of Non-Methane Hydrocarbons in Emissions from Biomass Burning

The stable carbon isotope ratios of nonmethane hydrocarbons (NMHC) and methyl chloride emitted from biomass burning were determined by analyzing seven whole air samples collected during different phases of the burning process as part of a laboratory study of wood burning. The average of the stable carbon isotope ratios of emitted alkanes, alkenes and aromatic compounds is identical to that of the burnt fuel; more than 50% of the values are within a range of ±1.5‰ of thecomposition of the burnt fuel wood. Thus for the majority of NMHC emitted from biomass burning stable carbon isotope ratio of the burnt fuel a good first order approximation for the isotopic composition of the emissions. Of the more than twenty compounds we studied, only methyl chloride and ethyne differed in stable carbon isotope ratios by more than a few per mil from the composition of the fuel. Ethyne is enriched in 13C by approximately 20–30‰, and most of the variability can beexplained by a dependence on flame temperature. The δ 13C values decreaseby 0.019 ‰/K (±0.0053‰/K) with increasing temperature. Methyl chloride is highly depleted in 13C, on average by25‰. However the results cover a wide range of nearly 30‰. Specifically, in two measurements with wood from Eucalyptus (Eucalyptus delegatensis) as fuel we observed the emission of extremely light methyl chloride (–68.5‰and–65.5‰). This coincides with higher than average emission ratiosfor methyl chloride (15.5 × 10−5 and 18 ×10−5 mol CH3Cl/mol CO2). These high emission ratios are consistent with the highchlorine content of the burnt fuel, although, due to the limited number of measurements, it would be premature to generalize these findings. The limited number of observations also prevents any conclusion on a systematic dependence between chlorine content of the fuel, emission ratios and stable carbon isotope ratio of methyl chloride emissions. However, our results show that a detailed understanding of the emissions of methyl chloride from chloride rich fuels is important for understanding its global budget. It is also evident that the usefulness of stable carbon isotope ratios to constrain the global budget of methyl chloride will be complicated by the very large variability of the stable carbon isotope ratio of biomass burning emissions. Nevertheless, ultimately the large fractionation may provide additional constraints for the contribution of biomass burning emissions to the atmospheric budget of methyl chloride.