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Optical Properties of Emissions from Laboratory Peat Combustion

机译:实验室泥炭燃烧排放的光学特性

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Globally, organic soils and peats may store as much as 600 Gt of terrestrial carbon, representing 20 - 30% of the planet's terrestrial organic carbon mass. This is approximately the same carbon mass as that contained in Earth's atmosphere, despite peatlands occupying only 3% of its surface. Effects of increasing fire frequency and size in these ecosystems are of global concern due to the potential for enormous carbon release into the atmosphere with significant implications for the global carbon cycle and radiative forcing. Combustion of peat mostly takes place in the low temperature, smoldering phase of a fire. It consumes carbon that may have accumulated over a period of hundreds to thousands of years. In comparison, combustion of aboveground biomass fuels releases carbon that has accumulated much more recently, generally over a period of years or decades. Here, we present the aerosol optical properties from the controlled laboratory combustion of peat soil samples from three regions, Siberia (Russia) and Alaska and Florida (USA). Aerosol absorption and scattering coefficients measured using a three-wavelengths photoacoustic instrument were analyzed for single scattering albedo (SSA) and absorption Angstrom coefficient (AAC) and compared with previously reported values for other common wildland fuels. The mean organic mass-normalized absorption cross-section (MAC) of peat samples was found to be quite low, ranging from as low as 0.001 m~2g~(-1) at 781 nm to as high as 0.32 at 405 nm; however, combustion emissions from all peat samples depicted large AAC. While SSA values (0.9-1.0 at 405 nm) were similar to those from other wildland fuels, AAC values, (4.5-7.2 range at 405-870 nm) were substantially higher for emissions from peat combustion. These results have important implications for radiative forcing, actinic fluxes driving photochemistry, and optical source apportionment. Three fuel moisture levels were used in this work to enable us to determine whether peat sources or fuel moisture content were more important for the optical characteristics of combustion emissions. Results showed that SSA and AAC vary with moisture content-higher moisture content results in higher SSA values and lower spectral dependence of AAC. Florida lake peat (at 10% moisture level) exhibited the highest AAC value (~7.2).
机译:在全球范围内,有机土壤和泥炭可以储存多达600 Gt的陆地碳,占地球陆地有机碳质量的20-30%。尽管泥炭地仅占据地球表面的3%,但其碳含量与地球大气中的碳含量大致相同。在这些生态系统中,不断增加的火灾频率和规模所产生的影响是全球关注的问题,这是因为有可能向大气中大量释放碳,这对全球碳循环和辐射强迫具有重大影响。泥炭的燃烧大部分发生在火灾的低温闷燃阶段。它消耗的碳可能累积了数百到数千年。相比之下,地上生物质燃料的燃烧释放的碳,其积累的时间要长得多,通常是数年或数十年。在这里,我们介绍了来自三个地区(西伯利亚(俄罗斯),阿拉斯加和佛罗里达州(美国))的泥炭土壤样品受控实验室燃烧的气溶胶光学特性。分析了使用三波长光声仪器测量的气溶胶吸收和散射系数的单次散射反照率(SSA)和吸收埃系数(AAC),并将其与先前报告的其他常见野地燃料值进行了比较。泥炭样品的平均有机物质量归一化吸收截面(MAC)非常低,范围从781 nm的0.001 m〜2g〜(-1)到405 nm的0.32高。但是,所有泥炭样品的燃烧排放都显示出较大的AAC。尽管SSA值(在405 nm处为0.9-1.0)与其他野外燃料的相似,但AAC值(405-870 nm处在4.5-7.2的范围内)对于泥炭燃烧的排放而言要高得多。这些结果对辐射强迫,驱动光化学的光化通量和光源分配具有重要意义。在这项工作中使用了三种燃料水分含量,以使我们能够确定泥炭源或燃料水分含量对燃烧排放物的光学特性是否更为重要。结果表明,SSA和AAC随水分含量而变化-水分含量越高,SSA值越高,AAC的光谱依赖性越低。佛罗里达湖泥炭(湿度为10%)显示出最高的AAC值(约7.2)。

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