Design and evaluation of a long-term soil gas flux sampler

1992 ◽  
Vol 26 (4) ◽  
pp. 709-714 ◽  
Author(s):  
Stuart A. Batterman ◽  
Brian C. McQuown ◽  
Prahlad N. Murthy ◽  
Andrew R. McFarland
Keyword(s):  
Soil Gas ◽  
Gas Flux ◽  
2020 ◽  
Vol 13 (12) ◽  
pp. 6657-6673
Author(s):  
Noriko Nakayama ◽  
Yo Toma ◽  
Yusuke Iwai ◽  
Hiroshi Furutani ◽  
Toshinobu Hondo ◽  
...  

Abstract. We developed a mass spectrometric soil-gas flux measurement system using a portable high-resolution multi-turn time-of-flight mass spectrometer, called MULTUM, and we combined it with an automated soil-gas flux chamber for the continuous field measurement of multiple gas concentrations with a high temporal resolution. The developed system continuously measures the concentrations of four different atmospheric gases (NO2, CH4, CO2, and field soil–atmosphere flux measurements of greenhouse gases (NO2, O2) ranging over 6 orders of magnitude at one time using a single gas sample. The measurements are performed every 2.5 min with an analytical precision (2 standard deviations) of ±34 ppbv for NO2; ±170 ppbv, CH4; ±16 ppmv, CO2; and ±0.60 vol %, O2 at their atmospheric concentrations. The developed system was used for the continuous field soil–atmosphere flux measurements of greenhouse gases (NO2, CH4, and CO2) and O2 with a 1 h resolution. The minimum quantitative fluxes (2 standard deviations) were estimated via a simulation as 70.2 µgNm-2h-1 for NO2; 139 µgCm-2h-1, CH4; 11.7 mg C m−2 h−1, CO2; and 9.8 g O2 m−2 h−1, O2. The estimated minimum detectable fluxes (2 standard deviations) were 17.2 µgNm-2h-1 for NO2; 35.4 µgCm-2h-1, CH4; 2.6 mg C m−2 h−1, CO2; and 2.9 g O2 m−2 h−1, O2. The developed system was deployed at the university farm of the Ehime University (Matsuyama, Ehime, Japan) for a field observation over 5 d. An abrupt increase in NO2 flux from 70 to 682 µgNm-2h-1 was observed a few hours after the first rainfall, whereas no obvious increase was observed in CO2 flux. No abrupt NO2 flux change was observed in succeeding rainfall events, and the observed temporal responses at the first rainfall were different from those observed in a laboratory experiment. The observed differences in temporal flux variation for each gas component show that gas production processes and their responses for each gas component in the soil are different. The results of this study indicate that continuous multiple gas concentration and flux measurements can be employed as a powerful tool for tracking and understanding underlying biological and physicochemical processes in the soil by measuring more tracer gases such as volatile organic carbon, reactive nitrogen, and noble gases, and by exploiting the broad versatility of mass spectrometry in detecting a broad range of gas species.


2019 ◽  
Vol 95 (5) ◽  
Author(s):  
Ianina Altshuler ◽  
Jennifer Ronholm ◽  
Alice Layton ◽  
Tullis C Onstott ◽  
Charles W. Greer ◽  
...  

2020 ◽  
Author(s):  
Noriko Nakayama ◽  
Yo Toma ◽  
Yusuke Iwai ◽  
Hiroshi Furutani ◽  
Toshinobu Hondo ◽  
...  

Abstract. We developed a mass spectrometric soil-gas flux measurement system using a portable high-resolution multi-turn time-of-flight mass spectrometer, called MULTUM, combined with an automated soil-gas flux chamber for continuous field measurement of multiple gas concentrations. The developed system continuously measures concentrations of four different atmospheric gases (i.e., N2O, CH4, CO2, and O2), of which the concentrations range over six orders of magnitude at a time within a single gas sample. The measurements were performed every 2.5 min with analytical precisions (two standard deviations) of ±34 ppbv for N2O, ±170 ppbv for CH4, ±16 ppmv for CO2, and ±0.60 vol% for O2 at their atmospheric concentrations. The developed system was used for continuous field soil–atmosphere flux measurements of greenhouse gases (GHGs: N2O, CH4, and CO2) and O2 with 1 h resolution. The minimum quantitative fluxes (two standard deviations) were estimated through simulation as 70.2 µg N m−2 h−1 for N2O, 139 µg C m−2 h−1 for CH4, 11.7 mg C m−2 h−1 for CO2, and 9.8 g O2 m−2 h−1 (negative) for O2, whereas the estimated minimum detectable fluxes (two standard deviations) were 17.2 μg N m−2 h −1 for N2O, 35.4 μg C m−2 h−1 for CH4, 2.6 mg C m−2 h−1 for CO2, and 2.9 g O2 m−2 h−1 for O2. The developed system was deployed in the University Farm of the Ehime University (Matsuyama, Ehime, Japan) for a field observation over five days. Interestingly, an abrupt increase in N2O flux from 70 to 682 µg N m−2 h−1 was observed a few hours after the first rainfall, whereas no obvious increase in the CO2 flux was observed, although the temporal responses were different from those observed in a laboratory experiment. No abrupt N2O flux change was observed in succeeding rainfalls. Continuous multiple-gas flux and concentration measurements can be a powerful tool for tracking and understanding of underlying biological and physicochemical processes in the soil through measuring more tracer gases, such as volatile organic carbon gases, reactive-nitrogen gases, and noble gases by taking advantage of the broad versatility of mass spectrometry in detecting broad range of gas species.


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