Kayler Zachary E, Sulzman Elizabeth W, Marshall John D, Mix Alan, Rugh William D, Bond Barbara J
Department of Forest Science, Oregon State University, 321 Richardson Hall, Corvallis, OR 97331, USA.
Rapid Commun Mass Spectrom. 2008 Aug;22(16):2533-8. doi: 10.1002/rcm.3643.
The stable isotopic composition of soil (13)CO(2) flux is important for monitoring soil biological and physical processes. While several methods exist to measure the isotopic composition of soil flux, we do not know how effective each method is at achieving this goal. To provide clear evidence of the accuracy of current measurement techniques we created a column filled with quartz sand through which a gas of known isotopic composition (-34.2 per thousand) and concentration (3,000 ppm) diffused for 7 h. We used a static chamber at equilibrium and a soil probe technique to test whether they could identify the isotopic signature of the known gas source. The static chamber is designed to identify the source gas isotopic composition when in equilibrium with the soil gas, and the soil probe method relies on a mixing model of samples withdrawn from three gas wells at different depths to identify the gas source. We sampled from ports installed along the side of the sand column to describe the isotopic and concentration gradient as well as to serve as a control for the soil probe. The soil probe produced similar isotopic and concentration values as the control ports, as well as Keeling intercepts. The static chamber at equilibrium did not identify the source gas but, when applied in a two end-member mixing model, did produce a similar Keeling intercept produced from the control ports. Neither of the methods was able to identify the source gas via the Keeling plot method probably because CO(2) profiles did not reach isotopic steady state. Our results showed that the static chamber at equilibrium should be used only with a Keeling plot approach and that the soil probe is able to provide estimates of uncertainty for the isotopic composition of soil gas as well as information pertinent to the soil profile.
土壤(13)CO(2)通量的稳定同位素组成对于监测土壤生物和物理过程至关重要。虽然存在几种测量土壤通量同位素组成的方法,但我们不知道每种方法在实现这一目标方面的效果如何。为了提供当前测量技术准确性的明确证据,我们创建了一个填充石英砂的柱体,一种已知同位素组成(-34.2‰)和浓度(3000 ppm)的气体在其中扩散了7小时。我们使用平衡状态下的静态箱和土壤探针技术来测试它们是否能够识别已知气体源的同位素特征。静态箱旨在识别与土壤气体平衡时的源气体同位素组成,土壤探针方法则依赖于从不同深度的三个气井中抽取的样品的混合模型来识别气体源。我们从沿砂柱侧面安装的端口进行采样,以描述同位素和浓度梯度,并作为土壤探针的对照。土壤探针产生的同位素和浓度值与对照端口相似,以及基林截距。处于平衡状态的静态箱没有识别出源气体,但在应用于两端元混合模型时,确实产生了与对照端口相似的基林截距。这两种方法都无法通过基林图方法识别源气体,可能是因为CO(2)剖面未达到同位素稳态。我们的结果表明,处于平衡状态的静态箱仅应与基林图方法一起使用,并且土壤探针能够提供土壤气体同位素组成的不确定性估计以及与土壤剖面相关的信息。