Stevenson David, Doherty Ruth, Sanderson Michael, Johnson Colin, Collins Bill, Derwent Dick
Institute for Atmospheric and Environmental Science, The University of Edinburgh, UK.
Faraday Discuss. 2005;130:41-57; discussion 125-51, 519-24. doi: 10.1039/b417412g.
Two coupled climate-chemistry model experiments for the period 1990-2030 were conducted: one with a fixed climate and the other with a varying climate forced by the is92a scenario. By comparing results from these experiments we have attempted to identify changes and variations in physical climate that may have important influences upon tropospheric chemical composition. Climate variables considered include: temperature, humidity, convective mass fluxes, precipitation, and the large-scale circulation. Increases in humidity, directly related to increases in temperature, exert a major influence on the budgets of ozone and the hydroxyl radical: decreasing 03 and increasing OH. Warming enhances decomposition of PAN, releasing NOx, and increases the rate of methane oxidation. Surface warming enhances vegetation emissions of isoprene, an important ozone precursor. In the changed climate, tropical convection generally reduces, but penetrates to higher levels. Over northern continents, convection tends to increase. These changes in convection affect both vertical mixing and lightning NOx emissions. We find no global trend in lightning emissions, but significant changes in its distribution. Changes in precipitation and the large-scale circulation are less important for composition, at least in these experiments. Higher levels of the oxidants OH and H202 lead to increases in aerosol formation and concentrations. These results indicate that climate-chemistry feedbacks are dominantly negative (less 03, a shorter CH4 lifetime, and more aerosol). The major mode of inter-annual variability in the is92a climate experiment is ENSO. This strongly modulates isoprene emissions from vegetation via tropical land surface temperatures. ENSO is also clearly the dominant source of variability in tropical column ozone, mainly through changes in the distribution of convection. The magnitude of inter-annual variability in ozone is comparable to the changes brought about by emissions and climate changes between the 1990s and 2020s, suggesting that it will be difficult to disentangle the different components of near-future changes.
针对1990 - 2030年期间开展了两项耦合的气候 - 化学模型实验:一项是固定气候条件下的实验,另一项是在is92a情景强迫下的变化气候条件下的实验。通过比较这些实验的结果,我们试图确定可能对对流层化学成分有重要影响的物理气候的变化和变异。所考虑的气候变量包括:温度、湿度、对流质量通量、降水和大尺度环流。湿度增加与温度升高直接相关,对臭氧和羟基自由基的收支有重大影响:臭氧减少而羟基增加。变暖增强了过氧乙酰硝酸酯(PAN)的分解,释放出氮氧化物(NOx),并提高了甲烷氧化速率。地表变暖增强了异戊二烯(一种重要的臭氧前体)的植被排放。在变化的气候中,热带对流总体上减少,但穿透到更高高度。在北半球大陆上空,对流趋于增加。这些对流变化影响垂直混合和闪电产生的氮氧化物排放。我们发现闪电排放没有全球趋势,但其分布有显著变化。降水和大尺度环流的变化对成分的影响较小,至少在这些实验中是这样。氧化剂羟基(OH)和过氧化氢(H2O2)水平升高导致气溶胶形成和浓度增加。这些结果表明气候 - 化学反馈主要是负反馈(臭氧减少、甲烷寿命缩短和气溶胶增多)。is92a气候实验中年际变率的主要模式是厄尔尼诺 - 南方涛动(ENSO)。这通过热带陆地表面温度强烈调节植被的异戊二烯排放。ENSO显然也是热带柱状臭氧变率的主要来源,主要通过对流分布的变化。臭氧中年际变率的幅度与20世纪90年代和20年代之间排放和气候变化所带来的变化相当,这表明很难区分近期变化的不同组成部分。