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In situ unsaturated zone water stable isotope (H-2 and O-18) measurements in semi-arid environments: a soil water balance

机译:半干旱环境中原位不饱和带水稳定同位素(H-2和O-18)的测量:土壤水平衡

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Stable isotopes (deuterium, H-2, and oxygen-18, O-18) of soil water were measured in the field using a liquid water isotope analyzer (tunable off-axis integrated cavity output spectroscope, OA-ICOS, LGR) and commercially available soil gas probes (BGL-30, UMS, Munich) in the semi-arid Cuvelai- Etosha Basin (CEB), Namibia. Results support the applicability of an in situ measurement system for the determination of stable isotopes in soil pore water. High spatial and temporal resolution was achieved in the study area with reasonable accuracy and measurements were in agreement with laboratory-based cryogenic vacuum extraction and subsequent cavity ring-down laser spectroscopic isotope analysis (CRDS, L2120-i, Picarro Inc.). After drift and span correction of the in situ isotope data, precision for over 140 measurements taken during two consecutive field campaigns (June and November 2014) was 1.8 and 0.48 parts per thousand for delta H-2 and delta O-18, respectively. Mean measurement trueness is determined using quality check standards and was 5 and 0.3 parts per thousand for delta H-2 and delta O-18, respectively. The isotope depth profiles are used quantitatively to calculate a soil water balance. The contribution of transpiration to total evapotranspiration ranged between 72 and 92 %. Shortly after a rain event, the contribution of transpiration was much lower, at 35 to 50 %. Potential limitations of such an in situ system are related to environmental conditions which could be minimized by using a temperature-controlled chamber for the laser spectrometer. Further, the applicability of the system using previously oven-dried soil material might be limited by physicochemical soil properties (i.e., clay minerals). Uncertainty in the in situ system is suggested to be reduced by improving the calibration procedure and further studying fractionation effects in-fluencing the isotope ratios in the soil water, especially at low water contents. Furthermore, the influence of soil-respired CO2 on isotope values within the root zone could not be deduced from the data.
机译:使用液态水同位素分析仪(可调离轴集成腔输出光谱仪,OA-ICOS,LGR)和商业化方法在田间测量土壤水的稳定同位素(氘,H-2和氧18,O-18)纳米比亚半干旱的Cuvelai-Etosha盆地(CEB)可用的土壤气体探头(BGL-30,UMS,慕尼黑)。结果支持原位测量系统在土壤孔隙水中测定稳定同位素的适用性。在研究区域内以合理的准确度实现了较高的时空分辨率,其测量结果与基于实验室的低温真空提取以及随后的腔衰荡激光光谱同位素分析(CRDS,L2120-i,Picarro Inc.)一致。在对原位同位素数据进行漂移和跨度校正后,两次连续野战(2014年6月和2014年11月)进行的140多次测量的精度分别为δH-2和δO-18千分之1.8和0.48千分之几。使用质量检查标准确定平均测量真实度,δH-2和δO-18分别为5和0.3千分之几。同位素深度剖面用于定量计算土壤水平衡。蒸腾作用对总蒸散量的贡献在72%至92%之间。雨后不久,蒸腾作用降低了很多,为35%至50%。这种原位系统的潜在局限性与环境条件有关,可以通过使用用于激光光谱仪的温度控制室来使其最小化。此外,使用先前烘箱干燥的土壤材料的系统的适用性可能受到物理化学土壤特性(即粘土矿物)的限制。建议通过改进校准程序并进一步研究影响土壤水中同位素比的分馏效应来降低原位系统的不确定性,尤其是在低含水量的情况下。此外,无法从数据推导出土壤呼吸的CO2对根区域内同位素值的影响。

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