scholarly journals A mass spectrometric multiple soil-gas flux measurement system with portable high-resolution mass spectrometer MULTUM coupled to automatic chamber for continuous field observation

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.

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.


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 ◽  

2015 ◽  
Vol 12 (17) ◽  
pp. 14593-14617 ◽  
Author(s):  
N. Pirk ◽  
M. Mastepanov ◽  
F.-J. W. Parmentier ◽  
M. Lund ◽  
P. Crill ◽  
...  

Abstract. The closed chamber technique is widely used to measure the exchange of methane (CH4) and carbon dioxide (CO2) from terrestrial ecosystems. There is, however, large uncertainty about which model should be used to calculate the gas flux from the measured gas concentrations. Due to experimental uncertainties the robust linear regression model (first order polynomial) is often applied, even though theoretical considerations of the technique suggest the application of other, curvilinear models. High-resolution automatic chamber systems which sample gas concentrations several hundred times per flux measurement make it possible to resolve the curvilinear behavior and study the information imposed by the natural variability of the temporal concentration changes. We used more than 50 000 such flux measurements of CH4 and CO2 from five field sites located in peat forming wetlands to calculate fluxes with different models. The flux differences from independent linear estimates are generally found to be smaller than the local flux variability on the plot scale. The curvilinear behavior of the gas concentrations within the chamber is strongly influenced by wind driven chamber leakage, and less so by changing gas concentration gradients in the soil during chamber closure. Such physical processes affect both gas species equally, which makes it possible to isolate biochemical processes affecting the gases differently, such as photosynthesis limitation by chamber headspace CO2 concentrations under high levels of incoming solar radiation. We assess the possibility to exploit this effect for a partitioning of the net CO2 flux into photosynthesis and ecosystem respiration and argue that high-resolution automatic chamber measurements could be used for purposes beyond the estimation of the net gas flux.


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

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