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Temporal and spatial variability of the stable isotopic composition of atmospheric molecular hydrogen: observations at six EUROHYDROS stations

机译:大气分子氢的稳定同位素组成的时间和空间变异:六个EurohydroS站的观察

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Despite the potential of isotope measurements to improve our understanding of the global atmospheric molecular hydrogen (H2) cycle, few H2 isotope data have been published so far. Now, within the EUROpean network for atmospheric HYDRogen Observations and Studies project (EUROHYDROS), weekly to monthly air samples from six locations in a global sampling network have been analysed for H2 mixing ratio (m(H2)) and the stable isotopic composition of the H2 ((D,H2), hereafter referred to as D). The time series thus obtained now cover one to five years for all stations. This is the largest set of ground station observations of D so far. Annual average D values are higher at the Southern Hemisphere (SH) than at the Northern Hemisphere (NH) stations; the maximum is observed at Neumayer (Antarctica), and the minimum at the non-arctic NH stations. The maximum seasonal differences in D range from ≈18 at Neumayer to ≈45 at Schauinsland (Southern Germany); in general, seasonal variability is largest at the NH stations. The timing of minima and maxima differs per station as well. In Alert (Arctic Canada), the variations in D and m(H2) can be approximated as simple harmonic functions with a ≈5-month relative phase shift. This out-of-phase seasonal behaviour of D and m(H2) can also be detected, but delayed and with a ≈6-month relative phase shift, at Mace Head and Cape Verde. However, no seasonal D cycle could be observed at Schauinsland, which likely reflects the larger influence of local sources and sinks at this continental station. At the two SH stations, no seasonal cycle could be detected in the D data. If it is assumed that the sink processes are the main drivers of the observed seasonality in m(H2) and D on the NH, the relative seasonal variations can be used to estimate the relative sink strength of the two major sinks, deposition to soils and atmospheric oxidation by the hydroxyl (OH) radical. For the NH coastal and marine stations this analysis suggests that the relative contribution of soil uptake to the total annual H2 removal increases with latitude.
机译:尽管有同位素测量的可能性来改善我们对全球大气分子氢(H2)循环的理解,但到目前为止已经发布了很少的H2同位素数据。现在,在欧洲大气氢观察和研究项目(EurohydroS)内,每周到每月到全局采样网络中的六个位置的空气样本已经分析了H 2混合比(M(H2))和稳定的同位素组成H2((d,h2),下文称为d)。如此获得的时间序列现在占据了所有站点的一到五年。这是迄今为止D的最大地面站观测。南半球(SH)的年平均D值高于北半球(NH)站;在Neumayer(南极洲)处观察到最大值,并且在非北极NH站处的最小值。 D Neumayer in Niceumayer至Zhauinsland(德国南部)的最大季节差异为≈45);通常,NH站的季节性变异性最大。最小值和最大值的时机也不同于电台。在警报(北极加拿大)中,D和M(H2)的变化可以近似为简单的谐波函数,具有≈5个月的相对相位偏移。也可以检测到D和M(H2)的这种不相间的季节性行为,但延迟并延迟了Mace Head和Cape Verde的≈6个月的相对相移。然而,在舒塞兰没有观察到季节性D循环,这可能反映了当地来源的较大影响和在这座大陆驻地的汇。在两个SH站,在D数据中没有检测到季节性循环。如果假设水槽过程是在M(H2)和D上观察到的季节性的主要驱动器,则可以使用相对季节性变化来估计两个主要水槽的相对沉降强度,沉积到土壤和土壤羟基(OH)自由基氧化大气氧化。对于NH沿海和海洋电台,该分析表明土壤吸收对年度H2的相对贡献随着纬度而增加。

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