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Chemical characterization of biogenic secondary organic aerosol generated from plant emissions under baseline and stressed conditions: inter- and intra-species variability for six coniferous species

机译:在基线和胁迫条件下植物排放物产生的生物性次级有机气溶胶的化学特征:六个针叶树种的种间和种内变异性

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摘要

The largest global source of secondary organic aerosol (SOA) in the atmosphere isderived from the oxidation of biogenic emissions. Plant stressors associatedwith a changing environment can alter both the quantity and composition ofthe compounds that are emitted. Alterations to the biogenic volatile organic compound (BVOC) profilecould impact the characteristics of the SOA formed from those emissions.This study investigated the impacts of one global change stressor, increasedherbivory, on the composition of SOA derived from real plant emissions.Herbivory was simulated via application of methyl jasmonate (MeJA), a proxycompound. Experiments were repeated under pre- and post-treatment conditionsfor six different coniferous plant types. Volatile organic compounds (VOCs) emitted from the plants wereoxidized to form SOA via dark ozone-initiated chemistry. The SOAchemical composition was measured using a Aerodyne high-resolution time-of-flightaerosol mass spectrometer (HR-AMS). The aerosol mass spectraof pre-treatment biogenic SOA from all plant types tended to be similar withcorrelations usually greater than or equal to 0.90. The presence of astressor produced characteristic differences in the SOA mass spectra.Specifically, the following were identified as a possible biogenicstress AMS marker with the corresponding HR ion(s) shown in parentheses: 31 (CHO), 58 (CHO,CHO), 29 (CH), 57(CHO), 59 (CHO,CHO), 71 (CHO,CHO), and 83 (CHO). The firstaerosol mass spectrum of SOA generated from the oxidation of the plantstress hormone, MeJA, is also presented. Elemental analysisresults demonstrated an O : C range of baseline biogenic SOA between 0.3 and 0.47.The O : C of standard MeJA SOA was 0.52. Results presented herecould be used to help identify a biogenic plant stress marker in ambientdata sets collected in forest environments.
机译:大气中最大的全球次级有机气溶胶(SOA)来源源自生物排放物的氧化。与环境变化相关的植物胁迫源可以改变排放化合物的数量和组成。生物挥发性有机化合物(BVOC)剖面的变化可能会影响由这些排放物形成的SOA的特性。本研究调查了一种全球变化压力源-食草动物对源自真实植物排放物的SOA组成的影响。代理化合物茉莉酸甲酯(MeJA)的应用。在预处理和后处理条件下针对六种不同的针叶植物类型重复了实验。从植物中散发出的挥发性有机化合物(VOC)通过暗臭氧引发的化学作用氧化为SOA。使用Aerodyne高分辨率飞行时间气溶胶质谱仪(HR-AMS)测量SOA化学成分。来自所有植物类型的预处理过的生物SOA的气溶胶质谱趋于相似,相关性通常大于或等于0.90。应力源的存在在SOA质谱图中产生特征差异。具体来说,以下是可能的生物应力AMS标记,括号中显示了相应的HR离子:31(CHO),58(CHO,CHO),29 (CH),57(CHO),59(CHO,CHO),71(CHO,CHO)和83(CHO)。还介绍了由植物胁迫激素MeJA氧化产生的SOA的第一气溶胶质谱。元素分析结果表明,基线生物源SOA的O:C范围在0.3到0.47之间。标准MeJA SOA的O:C为0.52。本文提供的结果可用于帮助识别森林环境中收集的环境数据集中的生物植物胁迫标记。

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