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The influence of biogenic emissions from Africa on tropical tropospheric ozone during 2006: A global modeling study

机译:全球模拟研究:2006年非洲生物排放对热带对流层臭氧的影响

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We have performed simulations using a 3-D global chemistry-transport model to investigate the influence that biogenic emissions from the African continent exert on the composition of the troposphere in the tropical region. For this purpose we have applied two recently developed biogenic emission inventories provided for use in large-scale global models (Granier et al., 2005; Lathière et al., 2006) whose seasonality and temporal distribution for biogenic emissions of isoprene, other volatile organic compounds and NO is markedly different. The use of the 12 year average values for biogenic emissions provided by Lathière et al. (2006) results in an increase in the amount of nitrogen sequestrated into longer lived reservoir compounds which contributes to the reduction in the tropospheric ozone burden in the tropics. The associated re-partitioning of nitrogen between PAN, HNO_3 and organic nitrates also results in a ~5% increase in the loss of nitrogen by wet deposition. At a global scale there is a reduction in the oxidizing capacity of the model atmosphere which increases the atmospheric lifetimes of CH_4 and CO by ~1.5% and ~4%, respectively. Comparisons against a range of different measurements indicate that applying the 12 year average of Lathière et al. (2006) improves the performance of TM4-AMMA for 2006 in the tropics. By the use of sensitivity studies we show that the release of NO from soils in Africa accounts for between ~2-45% of tropospheric ozone in the African troposphere, ~10% in the upper troposphere and between ~5-20% of the tropical tropo-spheric ozone column over the tropical Atlantic Ocean. The subsequent reduction in OH over the source regions allows enhanced transport of CO out of the region. For biogenic volatile organic C1 to C3 species released from Africa, the effects on tropical tropospheric ozone are rather limited, although this source contributes to the global burden of VOC by between ~2-4% and has a large influence on the organic composition of the troposphere over the tropical Atlantic Ocean.
机译:我们使用3-D全球化学运输模型进行了模拟,以研究非洲大陆的生物排放物对热带地区对流层组成的影响。为此,我们应用了两个最新开发的生物排放清单,这些清单可用于大规模全球模型(Granier等,2005;Lathière等,2006),其异戊二烯,其他挥发性有机物的生物排放的季节性和时间分布。化合物与NO明显不同。使用Lathière等人提供的12年平均值作为生物排放量。 (2006年)导致固存到寿命更长的储层化合物中的氮含量增加,这有助于减少热带对流层臭氧的负担。 PAN,HNO_3和有机硝酸盐之间相关的氮重新分配也会使湿法沉积造成的氮损失增加约5%。在全球范围内,模型大气的氧化能力下降,这使CH_4和CO的大气寿命分别增加了约1.5%和约4%。对一系列不同测量值的比较表明,应用Lathière等人的12年平均值。 (2006)提高了TM4-AMMA在热带地区2006年的性能。通过敏感性研究,我们发现非洲土壤中NO的释放量占非洲对流层对流层臭氧的约2-45%,对流层上层约10%,热带对流层的约5-20%热带大西洋上空的对流层臭氧柱。源区域上的OH的后续减少可增强CO从该区域向外的传输。对于从非洲释放的生物成因挥发性有机C1至C3物种,对热带对流层臭氧的影响相当有限,尽管该来源对全球VOC的负担贡献了约2-4%,并且对该物种的有机组成有很大影响。热带大西洋的对流层。

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