首页> 外文期刊>Journal of Geophysical Research. Biogeosciences >DIEL VARIATIONS OF H2O2 IN GREENLAND - A DISCUSSION OF THE CAUSE AND EFFECT RELATIONSHIP
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DIEL VARIATIONS OF H2O2 IN GREENLAND - A DISCUSSION OF THE CAUSE AND EFFECT RELATIONSHIP

机译:格陵兰H2O2的Diel变化-原因和效果关系的讨论。

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Atmospheric hydrogen peroxide (H2O2) measurements at Summit, Greenland, in May-June, 1993 exhibited a diel variation, with afternoon highs typically 1-2 parts per billion by volume (ppbv) and nighttime lows about 0.5 ppbv lower, This variation closely followed that for temperature; specific humidity exhibited the same general trend, During a 17-day snowfall-free period, surface snow was accumulating H2O2, apparently from nighttime cocondensation of H2O and H2O2. Previous photochemical modeling (Neftel et al., 1995) suggests that daytime H2O2 should be about I ppbv, significantly lower than our measured values, Previous equilibrium partitioning measurements between ice and gas phase (Conklin et al., 1993) suggest that air in equilibrium with H2O2 concentrations measured in surface snow (15-18 mu M) should have an H2O2 concentration 2-3 times what we measured 0.2-3.5 m above the snow surface, A simple eddy diffusion model, with vertical eddy diffusion coefficients calculated from balloon soundings, suggested that atmospheric H2O2 concentrations should be affected by any H2O2 degassed from surface snow, However, field measurements showed the absence of either high concentrations of H2O2 or a measurable concentration gradient between inlets 0.2 and 3 m above the snow. A surface resistance to degassing, that is, slow release of H2O2 from the ice matrix, is a plausible explanation for the differences between observations and modeled atmospheric profiles, Degassing of H2O2 at a rate below our detection limit would still influence measured atmospheric concentrations and help explain the difference between measurements and photochemical modeling, The cumulative evidence suggests that surface snow adjusts slowly to drops in atmospheric H2O2 concentration, over timescales of at least weeks. The H2O2 losses previously observed in pits sampled over more than 1 year are thought to have occurred later in the summer or fall, after the May-July field season. [References: 13]
机译:1993年5月至6月在格陵兰的Summit进行的大气过氧化氢(H2O2)测量显示出狄尔变化,下午的高点通常为ppbv的十亿分之1-2(ppbv),夜间的低点约为0.5 ppbv,这一变化紧随温度相对湿度表现出相同的总体趋势。在没有降雪的17天期间,表面积雪显然是由H2O2和H2O2的夜间共冷凝引起的。以前的光化学模型(Neftel等,1995)表明白天的H2O2应该约为1 ppbv,大大低于我们的测量值。先前的冰和气相之间的平衡分配测量(Conklin等,1993)表明空气处于平衡状态在表层雪(15-18μM)中测得的H2O2浓度应为我们在雪面上方0.2-3.5 m处测得的H2O2浓度的2-3倍,这是一个简单的涡流扩散模型,其垂直涡流扩散系数由气球测深计算得出,建议大气中的H2O2浓度应该受到从表雪中脱气的任何H2O2的影响。但是,现场测量表明,在雪上方0.2和3 m的入口之间既没有高浓度的H2O2也不存在可测量的浓度梯度。表面脱气的阻力,即H2O2从冰基质中的缓慢释放,是对观测值与模拟大气剖面之间差异的合理解释。以低于我们的检测极限的速率对H2O2脱气仍会影响测得的大气浓度并有助于解释了测量和光化学模型之间的区别。累积的证据表明,在至少几周的时间范围内,表面积雪会缓慢调整以适应大气H2O2浓度的下降。以前在超过1年的采样坑中观察到的H2O2损失被认为是在5月至7月的田间季节之后的夏季或秋季晚些时候发生的。 [参考:13]

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