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The influence of snow grain size and impurities on the vertical profiles of actinic flux and associated NOx emissions on the Antarctic and Greenland ice sheets

机译:雪粒大小和杂质对南极和格陵兰冰原上光化通量的垂直剖面及相关NOx排放的影响

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摘要

We use observations of the absorption properties of black carbon and non-black carbon impurities in near-surface snow collected near the research stations at South Pole and Dome C, Antarctica, and Summit, Greenland, combined with a snowpack actinic flux parameterization to estimate the vertical profile and e-folding depth of ultraviolet/near-visible (UV/near-vis) actinic flux in the snowpack at each location. We have developed a simple and broadly applicable parameterization to calculate depth and wavelength dependent snowpack actinic flux that can be easily integrated into large-scale (e.g., 3-D) models of the atmosphere. The calculated e-folding depths of actinic flux at 305 nm, the peak wavelength of nitrate photolysis in the snowpack, are 8–12 cm near the stations and 15–31 cm away (>11 km) from the stations. We find that the e-folding depth is strongly dependent on impurity content and wavelength in the UV/near-vis region, which explains the relatively shallow e-folding depths near stations where local activities lead to higher snow impurity levels. We calculate the lifetime of NO in the snowpack interstitial air produced by photolysis of snowpack nitrate against wind pumping (T) from the snowpack, and compare this to the calculated lifetime of NO against chemical conversion to HNO (T) to determine whether the NO produced at a given depth can escape from the snowpack to the overlying atmosphere. Comparison of T and T suggests efficient escape of photo produced NO in the snowpack to the overlying atmosphere throughout most of the photochemically active zone. Calculated vertical actinic flux profiles and observed snowpack nitrate concentrations are used to estimate the potential flux of NO from the snowpack. Calculated NO fluxes of 4.4 × 10–3.8 × 10 molecules cm s in remote polar locations and 3.2–8.2 × 10 molecules cm s near polar stations for January at Dome C and South Pole and June at Summit suggest that NO flux measurements near stations may be underestimating the amount of NO emitted from the clean polar snowpack.
机译:我们使用对南极,南极洲Dome C和格陵兰岛Summit的研究站附近收集的近地表雪中黑碳和非黑碳杂质的吸收特性的观察,结合雪堆光化通量参数化来估算积雪中每个位置的紫外线/近视(UV /近视)光化通量的垂直剖面和电子折叠深度。我们已经开发了一种简单且可广泛应用的参数化方法,可以计算与深度和波长相关的积雪光化通量,可以轻松地将其集成到大气的大规模(例如3-D)模型中。计算得出的光化通量在305 nm处的电子折叠深度(雪堆中硝酸盐光解的峰值波长)在站点附近为8–12 cm,而在站点附近为15–31 cm(> 11 km)。我们发现电子折叠深度很大程度上取决于紫外线/近视区域中的杂质含量和波长,这解释了在局部活动导致较高的雪杂质水平的站点附近电子折叠深度相对较浅。我们计算了雪堆硝酸盐对雪堆中的风抽(T)进行光解而产生的雪堆填隙空气中NO的寿命,并将其与计算得出的NO相对于化学转化为HNO(T)的NO寿命进行比较,以确定是否产生了NO在给定深度处,可以从雪堆中逃逸到上层大气。 T和T的比较表明,在整个光化学活性区域中,雪堆中产生的NO有效逃逸到上层大气中。计算出的垂直光化通量分布图和观察到的积雪的硝酸盐浓度可用于估算积雪中NO的潜在通量。在Dome C和South Pole的一月和在Summit的六月,在偏远极地的NO的通量为4.4×10–3.8×10分子cm s,在极地站附近为3.2–8.2×10分子cm s,这表明在站附近的NO通量测量可能低估了清洁极地积雪排放的NO的量。

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