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Surface and Boundary Layer Exchanges of Volatile Organic Compounds, Nitrogen Oxides and Ozone During the GABRIEL Campaign

机译:GABRIEL战役期间挥发性有机化合物,氮氧化物和臭氧的表面和边界层交换

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摘要

Abstract. We present an evaluation of sources, sinks and turbulent transport of nitrogen oxides, ozone and volatile organic compounds (VOC) in the boundary layer over French Guyana and Suriname during the October 2005 GABRIEL campaign by simulating observations with a single-column chemistry and climate model (SCM) along a zonal transect. Simulated concentrations of O3 and NO as well as NO2 photolysis rates over the forest agree well with observations when a small soil-biogenic NO emission flux was applied. This suggests that the photochemical conditions observed during GABRIEL reflect a pristine tropical low-NOx regime. The SCM uses a compensation point approach to simulate nocturnal deposition and daytime emissions of acetone and methanol and produces daytime boundary layer mixing ratios in reasonable agreement with observations. The area average isoprene emission flux, inferred from the observed isoprene mixing ratios and boundary layer height, is about half the flux simulated with commonly applied emission algorithms. The SCM nevertheless simulates too high isoprene mixing ratios, whereas hydroxyl concentrations are strongly underestimated compared to observations, which can at least partly explain the discrepancy. Furthermore, the model substantially overestimates the isoprene oxidation products methlyl vinyl ketone (MVK) and methacrolein (MACR) partly due to a simulated nocturnal increase due to isoprene oxidation. This increase is most prominent in the residual layer whereas in the nocturnal inversion layer we simulate a decrease in MVK and MACR mixing ratios, assuming efficient removal of MVK and MACR. Entrainment of residual layer air masses, which are enhanced in MVK and MACR and other isoprene oxidation products, into the growing boundary layer poses an additional sink for OH which is thus not available for isoprene oxidation. Based on these findings, we suggest pursuing measurements of the tropical residual layer chemistry with a focus on the nocturnal depletion of isoprene and its oxidation products.
机译:抽象。我们通过模拟单柱化学和气候模型的观测资料,对法国圭亚那和苏里南边界层上的氮氧化物,臭氧和挥发性有机化合物(VOC)的来源,汇和湍流传输进行了评估,方法是在2005年10月的GABRIEL运动期间进行。 (SCM)沿地带剖面。当使用少量土壤生物源性NO排放通量时,森林中的O3和NO的模拟浓度以及NO2的光解速率与观察结果非常吻合。这表明GABRIEL期间观察到的光化学条件反映了原始的热带低NOx状况。 SCM使用补偿点方法模拟夜间沉积和丙酮和甲醇的白天排放,并产生与观察值合理吻合的白天边界层混合比。从观察到的异戊二烯混合比和边界层高度推断出的异戊二烯面积平均排放通量大约是常用排放算法模拟的通量的一半。然而,SCM模拟的异戊二烯混合比例太高,而与观察值相比,羟基浓度被大大低估了,这至少可以部分解释这一差异。此外,该模型实质上高估了异戊二烯的氧化产物甲基烯丙基乙烯基酮(MVK)和甲基丙烯醛(MACR)的部分原因是由于异戊二烯氧化引起的模拟夜间活动增加。假设有效去除了MVK和MACR,则这种增加在残留层中最为明显,而在夜间反转层中,我们模拟了MVK和MACR混合比的降低。在MVK和MACR以及其他异戊二烯氧化产物中增加的残留层空气质量被夹带到生长的边界层中,构成了额外的OH吸收池,因此无法用于异戊二烯氧化。基于这些发现,我们建议对热带残留层化学物质进行测量,重点是异戊二烯及其氧化产物的夜间消耗。

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