Contaminant Vapors as a Component of Soil Gas in the Unsaturated Zone

Author(s):  
Warren J. Lyman ◽  
Patrick J. Reidy ◽  
Benjamin Levy ◽  
Chi-Yuan Fan
Keyword(s):  
2003 ◽  
Vol 23 (2) ◽  
pp. 73-83
Author(s):  
David W. Ostendorf ◽  
Erich S. Hinlein ◽  
Alan J. Lutenegger ◽  
Pierre S. Tehrany

Radiocarbon ◽  
2013 ◽  
Vol 55 (2) ◽  
pp. 932-942 ◽  
Author(s):  
I Carmi ◽  
D Yakir ◽  
Y Yechieli ◽  
J Kronfeld ◽  
M Stiller

A study of CO2 in soil gas was conducted in a bare plot in the unsaturated zone (USZ) of Yatir Forest, northern Negev, Israel. In 2006, 6 tubes for sampling of soil gas were inserted into the USZ to depths of 30, 60, 90, 120, 200, and 240 cm. Profiles of soil gas in the USZ were collected from the tubes 5 times between October 2007 and September 2008. Measurements of the collected profiles of soil gas were of CO2 (ppm), δ13C (′), and Δ14C (′). At all times, the concentration of CO2 in the soil gas was higher than in the air at the surface (CO2 ≃ 400 ppm; δ13C ≃ −9′). The main source of the CO2 in soil gas is from biotic activity released through roots of trees and of seasonal plants close to the surface. In the winter, the CO2 concentrations were lowest (6000 ppm) and the δ13C was −20′. In the spring and through the summer, the CO2 concentration increased. It was estimated that the major source of CO2 is at ≃240 cm depth (δ13C ≃ −22′; CO2 ≃ 9000 ppm) or below. Above this level, the concentrations decrease and the δ13C (′) become more positive. The 14C values in the measured profile are all less than atmospheric and biotic 14C. It was deduced that biotic CO2 dissolves in porewater to form carbonic acid, which then dissolves secondary carbonate (δ13C ≃ −8′; 14C ≃ −900′) from the sediments of the USZ. With the 14C data, the subsequent release of CO2 into the soil gas was then estimated. The 14C data, supported by the 13C and CO2 data, also indicate a biotic source at the root zone, at about 90 cm depth.


1991 ◽  
Vol 24 (11) ◽  
pp. 127-138
Author(s):  
R. C. A. Hirata ◽  
R. W. Cleary

In 1983, a serious accident occurred in Porto Feliz, São Paulo, Brazil when the rupture of a storage tank released 400,000 litres of volatile organic solvents. A large portion of the underlying aquifer was contaminated including some deep wells and shallow hand-dug wells. Soil-gas sampling was the technique used to evaluate the degree and extent of contamination. The method is based on the analysis of small quantities of soil vapors extracted at shallow depths. The origin of these vapors is the underlying contaminated groundwater and the vapor concentration distribution reflects the degree and extent of aquifer contamination. Other techniques were rejected since the physico-chemical characteristics of the pollutants did not allow their detection by traditional geophysical methods and the thick unsaturated zone and difficult geology would have resulted in exorbitant drilling costs for monitoring wells. The use of soil-gas sampling allowed mapping of the pollution plume, defining its two-dimensional shape and location. Vapor analyses at different depths permitted the establishment of concentration gradients and an estimation of vertical vapor flow behavior in the unsaturated zone as well as surface losses by volatilization. Water levels in existing wells made it possible to construct potentiometric surface maps, defining the groundwater flow pattern. Periodic groundwater quality monitoring furnished data for the evaluation of the plume migration velocity and the influence of rainfall on the increase of pollutant concentrations in the aquifer. The groundwater pollutant concentrations obtained gave a good correlation between the two means.


Radiocarbon ◽  
1989 ◽  
Vol 31 (03) ◽  
pp. 934-939 ◽  
Author(s):  
Lorenz Eichinger

Extensive investigations of isotope content and hydrochemical parameters in soil gas, soil material, groundwater and seepage water from a Quaternary aquifer show a good correlation between 14C concentration of the groundwater and its mean residence time in the unsaturated zone. The initial 14C concentration varies between 100 and 50% modern. It decreases through solution and dissolution of carbonates to 50% of the 14C concentration of atmospheric CO2.


2005 ◽  
Vol 33 (1) ◽  
pp. 373-376 ◽  
Author(s):  
Péter Hegymegi ◽  
Anita Gál ◽  
Imre Czinkota ◽  
Tony Vyn
Keyword(s):  
Soil Gas ◽  

2013 ◽  
Vol 2 (1) ◽  
pp. 22-26
Author(s):  
Joanna Czekaj ◽  
Kamil Trepka

Abstract Goczałkowice reservoir is one of the main source of drinking water for Upper Silesia Region. In reference to Water Frame Directive matter since 2010 the strategic research project: „Integrated system supporting management and protection of dammed reservoir (ZiZoZap)”, which is being conducted on Goczałkowice reservoir, has been pursued. In the framework of this project complex groundwater monitoring is carried on. One aspect is vadose zone research, conducted to obtain information about changes in chemical composition of infiltrating water and mass transport within this zone. Based on historical data and the structural model of direct catchment of Goczałkowice reservoir location of the vadose zone research site was selected. At the end of November 2012 specially designed lysimeter was installed with 10 MacroRhizon samplers at each lithological variation in unsaturated zone. This lysimeter, together with nested observation wells, located in the direct proximity, create the vadose zone research site which main aim is specifying the amount of nitrate transport in the vertical profile.


2001 ◽  
Author(s):  
Silvia Terziotti ◽  
Jo Leslie Eimers

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