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      FTIR time-series of biomass burning products (HCN, C<sub>2</sub>H<sub>6</sub>, C<sub>2</sub>H<sub>2</sub>, CH<sub>3</sub>OH, and HCOOH) at Reunion Island (21° S, 55° E) and comparisons with model data

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          Abstract

          <p><strong>Abstract.</strong> Reunion Island (21&amp;deg; S, 55&amp;deg; E), situated in the Indian Ocean at about 800 km east of Madagascar, is appropriately located to monitor the outflow of biomass burning pollution from Southern Africa and Madagascar, in the case of short-lived compounds, and from other Southern Hemispheric landmasses such as South America, in the case of longer-lived species. Ground-based Fourier transform infrared (FTIR) solar absorption observations are sensitive to a large number of biomass burning products. We present in this work the FTIR retrieval strategies, suitable for very humid sites such as Reunion Island, for hydrogen cyanide (HCN), ethane (C<sub>2</sub>H<sub>6</sub>), acetylene (C<sub>2</sub>H<sub>2</sub>), methanol (CH<sub>3</sub>OH), and formic acid (HCOOH). We provide their total columns time-series obtained from the measurements during August–October 2004, May–October 2007, and May 2009–December 2010. We show that biomass burning explains a large part of the observed seasonal and interannual variability of the chemical species. The correlations between the daily mean total columns of each of the species and those of CO, also measured with our FTIR spectrometer at Reunion Island, are very good from August to November (<i>R</i> &amp;geq; 0.86). This allows us to derive, for that period, the following enhancement ratios with respect to CO: 0.0047, 0.0078, 0.0020, 0.012, and 0.0046 for HCN, C<sub>2</sub>H<sub>6</sub>, C<sub>2</sub>H<sub>2</sub>, CH<sub>3</sub>OH, and HCOOH, respectively. The HCN ground-based data are compared to the chemical transport model GEOS-Chem, while the data for the other species are compared to the IMAGESv2 model. We show that using the HCN/CO ratio derived from our measurements (0.0047) in GEOS-Chem reduces the underestimation of the modeled HCN columns compared with the FTIR measurements. The comparisons between IMAGESv2 and the long-lived species C<sub>2</sub>H<sub>6</sub> and C<sub>2</sub>H<sub>2</sub> indicate that the biomass burning emissions used in the model (from the GFED3 inventory) are probably underestimated in the late September–October period for all years of measurements, and especially in 2004. The comparisons with the short-lived species, CH<sub>3</sub>OH and HCOOH, with lifetimes of around 5 days, suggest that the emission underestimation in late September–October 2004, occurs more specifically in the Southeastern Africa-Madagascar region. The very good correlation of CH<sub>3</sub>OH and HCOOH with CO suggests that, despite the dominance of the biogenic source of these compounds on the global scale, biomass burning is their major source at Reunion Island between August and November.</p>

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          Biomass burning in the tropics: impact on atmospheric chemistry and biogeochemical cycles.

          Biomass burning is widespread, especially in the tropics. It serves to clear land for shifting cultivation, to convert forests to agricultural and pastoral lands, and to remove dry vegetation in order to promote agricultural productivity and the growth of higher yield grasses. Furthermore, much agricultural waste and fuel wood is being combusted, particularly in developing countries. Biomass containing 2 to 5 petagrams of carbon is burned annually (1 petagram = 10(15) grams), producing large amounts of trace gases and aerosol particles that play important roles in atmospheric chemistry and climate. Emissions of carbon monoxide and methane by biomass burning affect the oxidation efficiency of the atmosphere by reacting with hydroxyl radicals, and emissions of nitric oxide and hydrocarbons lead to high ozone concentrations in the tropics during the dry season. Large quantities of smoke particles are produced as well, and these can serve as cloud condensation nuclei. These particles may thus substantially influence cloud microphysical and optical properties, an effect that could have repercussions for the radiation budget and the hydrological cycle in the tropics. Widespread burning may also disturb biogeochemical cycles, especially that of nitrogen. About 50 percent of the nitrogen in the biomass fuel can be released as molecular nitrogen. This pyrdenitrification process causes a sizable loss of fixed nitrogen in tropical ecosystems, in the range of 10 to 20 teragrams per year (1 teragram = 10(12) grams).
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            Emissions of primary aerosol and precursor gases in the years 2000 and 1750 prescribed data-sets for AeroCom

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              An Asian emission inventory of anthropogenic emission sources for the period 1980–2020

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                Author and article information

                Journal
                Atmospheric Chemistry and Physics
                Atmos. Chem. Phys.
                Copernicus GmbH
                1680-7324
                2012
                November 07 2012
                : 12
                : 21
                : 10367-10385
                Article
                10.5194/acp-12-10367-2012
                f252cbbb-12b0-439d-92e1-9c922b7af571
                © 2012

                https://creativecommons.org/licenses/by/3.0/

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