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The climate impact of ship NOx emissions: an improved estimate accounting for plume chemistry

机译:船上NOx排放对气候的影响:一种改进的估算方法,用于估算烟羽化学

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摘要

Nitrogen oxide (NO) emissions from maritime shipping produceozone (O) and hydroxyl radicals (OH), which in turn destroy methane(CH). The balance between this warming (due to O) and cooling(due to CH) determines the net effect of ship NO onclimate. Previous estimates of the chemical impact and radiative forcing (RF)of ship NO have generally assumed that plumes of ship exhaustare instantly diluted into model grid cells spanning hundreds of kilometers,even though this is known to produce biased results. Here we improve theparametric representation of exhaust-gas chemistry developed in the GEOS-Chemchemical transport model (CTM) to provide the first estimate of RF fromshipping that accounts for sub-grid-scale ship plume chemistry. The CTM nowcalculates O production and CH loss both within and outside theexhaust plumes and also accounts for the effect of wind speed. With theimproved modeling of plumes, ship NO perturbations are smallerthan suggested by the ensemble of past global modeling studies, but if weassume instant dilution of ship NO on the grid scale, the CTMreproduces previous model results. Our best estimates of the RF componentsfrom increasing ship NO emissions by 1 Tg(N) yr aresmaller than that given in the past literature: + 3.4 ±0.85 mW m (1σ confidence interval) from the short-livedozone increase, −5.7 ± 1.3 mW m from the CH decrease, and−1.7 ± 0.7 mW m from the long-lived O decrease thataccompanies the CH change. The resulting net RF is −4.0 ±2.0 mW m for emissions of 1 Tg(N) yr. Due to non-linearityin O production as a function of background NO, RF fromlarge changes in ship NO emissions, such as the increase sincepreindustrial times, is about 20% larger than this RF value for smallmarginal emission changes. Using sensitivity tests in one CTM, we quantifysources of uncertainty in the RF components and causes of the ±30%spread in past model results; the main source of uncertainty is thecomposition of the background atmosphere in the CTM, which is driven by modelformulation (±10 to 20%) and the plausible range of anthropogenicemissions (±10%).
机译:海上生产的臭氧(O)和羟基自由基(OH)排放的氮氧化物(NO)会破坏甲烷(CH)。这种变暖(归因于O)和冷却(归因于CH)之间的平衡决定了船舶NO对气候的净影响。以前对NO的化学影响和辐射强迫(RF)的先前估计通常假定船舶废气的烟气会立即稀释到跨越数百公里的模型网格中,即使已知会产生偏差的结果。在这里,我们改进了在GEOS-Chemical传输模型(CTM)中开发的废气化学的参数表示形式,以提供对来自电网的RF的第一个估计,该估计是次网格规模船羽化学的原因。现在,CTM可以计算排气羽流内部和外部的O生成量和CH损失,还可以计算风速的影响。随着羽流建模的改进,船舶NO的扰动比过去的全球建模研究的集成所建议的要小,但是如果我们假设船舶NO在网格规模上的即时稀释,则CTM会再现以前的模型结果。我们对船舶NO排放量每增加1 Tg(N)yr的射频分量的最佳估算值比过去的文献中的估算值要小:短期活动区增加+ 3.4±0.85 mW m(1σ置信区间),-5.7±1.3 mW CH降低的m值和长寿命O降低的−1.7±0.7 mW m伴随CH的变化。对于1 Tg(N)yr的发射,最终的净RF为-4.0±2.0 mW m。由于O生成的非线性是背景NO的函数,因此船舶NO排放量的大变化所产生的RF(例如,自工业化时代以来的增加)比小幅度排放变化的RF值大约20%。使用一个CTM中的灵敏度测试,我们可以量化RF组件中不确定性的来源以及过去模型结果中±30%扩展的原因。不确定性的主要来源是CTM中背景大气的成分,这是由模型公式化(±10%至20%)和人为排放的合理范围(±10%)驱动的。

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