G. Gonzalez-Gil
ETH Zurich
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Featured researches published by G. Gonzalez-Gil.
Waste Management | 2012
Martin H. Schroth; Werner Eugster; K.E. Gómez; G. Gonzalez-Gil; Pascal A. Niklaus; P. Oester
Landfills are a major anthropogenic source of the greenhouse gas methane (CH(4)). However, much of the CH(4) produced during the anaerobic degradation of organic waste is consumed by methanotrophic microorganisms during passage through the landfill-cover soil. On a section of a closed landfill near Liestal, Switzerland, we performed experiments to compare CH(4) fluxes obtained by different methods at or above the cover-soil surface with below-ground fluxes, and to link methanotrophic activity to estimates of CH(4) ingress (loading) from the waste body at selected locations. Fluxes of CH(4) into or out of the cover soil were quantified by eddy-covariance and static flux-chamber measurements. In addition, CH(4) concentrations at the soil surface were monitored using a field-portable FID detector. Near-surface CH(4) fluxes and CH(4) loading were estimated from soil-gas concentration profiles in conjunction with radon measurements, and gas push-pull tests (GPPTs) were performed to quantify rates of microbial CH(4) oxidation. Eddy-covariance measurements yielded by far the largest and probably most representative estimates of overall CH(4) emissions from the test section (daily mean up to ∼91,500μmolm(-2)d(-1)), whereas flux-chamber measurements and CH(4) concentration profiles indicated that at the majority of locations the cover soil was a net sink for atmospheric CH(4) (uptake up to -380μmolm(-2)d(-1)) during the experimental period. Methane concentration profiles also indicated strong variability in CH(4) loading over short distances in the cover soil, while potential methanotrophic activity derived from GPPTs was high (v(max)∼13mmolL(-1)(soil air)h(-1)) at a location with substantial CH(4) loading. Our results provide a basis to assess spatial and temporal variability of CH(4) dynamics in the complex terrain of a landfill-cover soil.
Journal of Geophysical Research | 2008
Karina Urmann; Martin H. Schroth; Matthias Noll; G. Gonzalez-Gil; Josef Zeyer
[1] Emissions of the greenhouse gas CH 4 , which is often produced in contaminated aquifers, are reduced or eliminated by microbial CH 4 oxidation in the overlying vadose zone. The aim of this field study was to estimate kinetic parameters and isotope fractionation factors for CH 4 oxidation in situ in the vadose zone above a methanogenic aquifer in Studen, Switzerland, and to characterize the involved methanotrophic communities. To quantify kinetic parameters, several field tests, so-called gas push-pull tests (GPPTs), with CH 4 injection concentrations ranging from 17 to 80 mL L -1 were performed. An apparent V max of 0.70 ±0.15 mmol CH 4 (L soil air) -1 h -1 and an apparent K m of 0.28 ± 0.09 mmol CH 4 (L soil air) -1 was estimated for CH 4 oxidation at 2.7 m depth, close to the groundwater table. At 1.1 m depth, K m (0.13 ± 0.02 mmol CH 4 (L soil air) -1 ) was in a similar range, but V max (0.076 ± 0.006 mmol CH 4 (L soil air) -1 h -1 ) was an order of magnitude lower. At 2.7 m, apparent first-order rate constants determined from a CH4 gas profile (1.9 h -1 ) and from a single GPPT (2.0 ± 0.03 h -1 ) were in good agreement. Above the groundwater table, a V max much higher than the in situ CH 4 oxidation rate prior to GPPTs indicated a high buffer capacity for CH 4 . At both depths, known methanotrophic species affiliated with Methylosarcina and Methylocystis were detected by cloning and sequencing. Apparent stable carbon isotope fractionation factors a for CH 4 oxidation determined during GPPTs ranged from 1.006 to 1.032. Variability was likely due to differences in methanotrophic activity and CH 4 availability leading to different degrees of mass transfer limitation. This complicates the use of stable isotopes as an independent quantification method.
Waste Management | 2009
K.E. Gómez; G. Gonzalez-Gil; A. Lazzaro; Martin H. Schroth
Methane (CH(4)) oxidation by aerobic methanotrophs in landfill-cover soils decreases emissions of landfill-produced CH(4) to the atmosphere. To quantify in situ rates of CH(4) oxidation we performed five gas push-pull tests (GPPTs) at each of two locations in the cover soil of the Lindenstock landfill (Liestal, Switzerland) over a 4 week period. GPPTs consist of the injection of a gas mixture containing CH(4), O(2) and noble gas tracers followed by extraction from the same location. Quantification of first-order rate constants was based upon comparison of breakthrough curves of CH(4) with either Ar or CH(4) itself from a subsequent inactive GPPT containing acetylene as an inhibitor of CH(4) oxidation. The maximum calculated first-order rate constant was 24.8+/-0.8 h(-1) at location 1 and 18.9+/-0.6 h(-1) at location 2. In general, location 2 had higher background CH(4) concentrations in vertical profile samples than location 1. High background CH(4) concentrations in the cover soil during some experiments adversely affected GPPT breakthrough curves and data interpretation. Real-time PCR verified the presence of a large population of methanotrophs at the two GPPT locations and comparison of stable carbon isotope fractionation of CH(4) in an active GPPT and a subsequent inactive GPPT confirmed that microbial activity was responsible for the CH(4) oxidation. The GPPT was shown to be a useful tool to reproducibly estimate in situ rates of CH(4) oxidation in a landfill-cover soil when background CH(4) concentrations were low.
Environmental Science & Technology | 2005
Karina Urmann; G. Gonzalez-Gil; Martin H. Schroth; Markus Hofer; Josef Zeyer
Vadose Zone Journal | 2007
Karina Urmann; G. Gonzalez-Gil; Martin H. Schroth; Josef Zeyer
Environmental Science & Technology | 2007
G. Gonzalez-Gil; Martin H. Schroth; Josef Zeyer
Environmental Science & Technology | 2008
Katherine Gómez; G. Gonzalez-Gil; Martin H. Schroth; Josef Zeyer
Geochimica et Cosmochimica Acta | 2008
G. Gonzalez-Gil; Martin H. Schroth; K.E. Gómez; Andreas Papritz; Josef Zeyer
International Congress Series | 2006
G. Gonzalez-Gil; Karina Urmann; K.E. Gómez; Martin H. Schroth; Josef Zeyer
Archive | 2003
Martin H. Schroth; Karina Urmann; G. Gonzalez-Gil; Josef Zeyer