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Atmospheric and ice core chemistry of hydroperoxides in West Antarctica: Links to stratospheric ozone and climate variability.

机译:西南极洲氢过氧化物的大气和冰芯化学性质:与平流层臭氧和气候多变性的联系。

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Current and past records of hydroperoxides in air, snow and firn of West Antarctica were investigated over 3 field seasons covering >5000 km and 24 sites. Concentrations of methylhydroperoxide (MHP), the only important organic atmospheric hydroperoxide found, were ten times the levels expected based on past photochemical modeling. Between 76 and 90°S, the snow pack is a net source for hydrogen peroxide (H2O2) but not for MHP in summer. There is strong evidence that low stratospheric ozone leads to increases of H2O2 at the surface. The modeled sensitivity of H2O2 and particularly MHP to nitrogen oxide (NO) shows that atmospheric hydroperoxides help constrain the NO background and thus estimate the past atmospheric oxidation capacity using ice cores. Century-scale H2O2 ice core records from 24 locations across the West Antarctic Ice Sheet (WAIS) were used to develop a regional semi-empirical deposition model, with accumulation rate and temperature as parameters. The model fit using longterm average H2O2 concentrations is consistent with an existing physically based atmosphere-to-snow transfer model and predicts 'effective' annual mean atmospheric H2O 2 mixing ratios of 1-3 pptv across the region, comparable to observations. Modeled sensitivities suggest that recent Antarctic temperature changes have no noticeable effect on the H2O2 record in the interior of WAIS and that accumulation rates dominate the interannual variability of H2O2 under the current temperature regime. This leads to the imprint of a large-scale climate signal in the H2O 2 record, with significant spectral peaks at ENSO-like periodicities (2-7 yr). Validation of results from the new ECMWF reanalysis (ERA-40) using accumulation records from the same cores showed that simulated accumulation rates are too low at 21 of the 22 ice core sites, averaging only 66% (range 34-22%) of the observed accumulation over 1958-2001. Compared to the pre-satellite era (1958-1977) total amounts of accumulation matched better and linear correlations improved after 1978, showing statistical significance at 10 of 22 core sites (0.11 r 0.73, p 0.1).
机译:对南极西部的空气,雪和火星中氢过氧化物的当前和过去记录进行了调查,涉及3个超过5000公里的野外季节,分布在24个地点。发现的唯一重要的有机大气氢过氧化物甲基氢过氧化物(MHP)的浓度是根据过去的光化学模型预期的十倍。在76至90°S之间,积雪是过氧化氢(H2O2)的净来源,但在夏天不是MHP的净来源。强有力的证据表明,低平流层臭氧会导致表面H2O2的增加。 H2O2(尤其是MHP)对氮氧化物(NO)建模的敏感性表明,大气过氧化氢有助于限制NO背景,从而使用冰芯估算过去的大气氧化能力。利用南极西部冰原(WAIS)上24个地点的世纪规模H2O2冰芯记录,以累积速率和温度为参数,建立了区域半经验沉积模型。使用长期平均H2O2浓度进行的模型拟合与现有的基于物理的大气到雪气转移模型一致,并预测该地区的“有效”年平均大气H2O2混合比为1-3 pptv,与观测值相当。模拟的敏感性表明,南极最近的温度变化对WAIS内部的H2O2记录没有明显影响,并且在当前温度条件下,累积速率主导了H2O2的年际变化。这导致在H2O 2记录中留下了大规模的气候信号,并在类似ENSO的周期性(2-7年)上出现了明显的光谱峰。使用来自相同岩心的累积记录对新ECMWF再分析(ERA-40)的结果进行验证,结果表明,在22个冰岩心站点中的21个中,模拟的蓄积率太低,平均仅占66%(范围34-22%)。在1958-2001年期间观察到的积累。与卫星前时代(1958-1977年)相比,1978年之后的总积累量更好,线性相关性得到改善,在22个核心站点中的10个显示了统计学意义(0.11

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