scholarly journals Integrating Source Apportionment Tracers into a Bottom-up Inventory of Methane Emissions in the Barnett Shale Hydraulic Fracturing Region

2015 ◽  
Vol 49 (13) ◽  
pp. 8175-8182 ◽  
Author(s):  
Amy Townsend-Small ◽  
Josette E. Marrero ◽  
David R. Lyon ◽  
Isobel J. Simpson ◽  
Simone Meinardi ◽  
...  
2019 ◽  
Vol 6 (8) ◽  
pp. 473-478 ◽  
Author(s):  
Jianxiong Sheng ◽  
Shaojie Song ◽  
Yuzhong Zhang ◽  
Ronald G. Prinn ◽  
Greet Janssens-Maenhout

2017 ◽  
Author(s):  
Marielle Saunois ◽  
Philippe Bousquet ◽  
Benjamin Poulter ◽  
Anna Peregon ◽  
Philippe Ciais ◽  
...  

Abstract. Following the recent Global Carbon project (GCP) synthesis of the decadal methane (CH4) budget over 2000–2012 (Saunois et al., 2016), we analyse here the same dataset with a focus on quasi-decadal and inter-annual variability in CH4 emissions. The GCP dataset integrates results from top-down studies (exploiting atmospheric observations within an atmospheric inverse-modelling frameworks) and bottom-up models, inventories, and data-driven approaches (including process-based models for estimating land surface emissions and atmospheric chemistry, inventories of anthropogenic emissions, and data-driven extrapolations). The annual global methane emissions from top-down studies, which by construction match the observed methane growth rate within their uncertainties, all show an increase in total methane emissions over the period 2000–2012, but this increase is not linear over the 13 years. Despite differences between individual studies, the mean emission anomaly of the top-down ensemble shows no significant trend in total methane emissions over the period 2000–2006, during the plateau of atmospheric methane mole fractions, and also over the period 2008–2012, during the renewed atmospheric methane increase. However, the top-down ensemble mean produces an emission shift between 2006 and 2008, leading to 22 [16–32] Tg CH4 yr−1 higher methane emissions over the period 2008–2012 compared to 2002–2006. This emission increase mostly originated from the tropics with a smaller contribution from mid-latitudes and no significant change from boreal regions. The regional contributions remain uncertain in top-down studies. Tropical South America and South and East Asia seems to contribute the most to the emission increase in the tropics. However, these two regions have only limited atmospheric measurements and remain therefore poorly constrained. The sectorial partitioning of this emission increase between the periods 2002–2006 and 2008–2012 differs from one atmospheric inversion study to another. However, all top-down studies suggest smaller changes in fossil fuel emissions (from oil, gas, and coal industries) compared to the mean of the bottom-up inventories included in this study. This difference is partly driven by a smaller emission change in China from the top-down studies compared to the estimate in the EDGARv4.2 inventory, which should be revised to smaller values in a near future. Though the sectorial partitioning of six individual top-down studies out of eight are not consistent with the observed change in atmospheric 13CH4, the partitioning derived from the ensemble mean is consistent with this isotopic constraint. At the global scale, the top-down ensemble mean suggests that, the dominant contribution to the resumed atmospheric CH4 growth after 2006 comes from microbial sources (more from agriculture and waste sectors than from natural wetlands), with an uncertain but smaller contribution from fossil CH4 emissions. Besides, a decrease in biomass burning emissions (in agreement with the biomass burning emission databases) makes the balance of sources consistent with atmospheric 13CH4 observations. The methane loss (in particular through OH oxidation) has not been investigated in detail in this study, although it may play a significant role in the recent atmospheric methane changes.


2018 ◽  
Vol 24 (6) ◽  
pp. 1051-1071 ◽  
Author(s):  
Miroslaw Zimnoch ◽  
Jaroslaw Necki ◽  
Lukasz Chmura ◽  
Alina Jasek ◽  
Dorota Jelen ◽  
...  

2019 ◽  
Vol 19 (4) ◽  
pp. 2561-2576 ◽  
Author(s):  
Anna Karion ◽  
Thomas Lauvaux ◽  
Israel Lopez Coto ◽  
Colm Sweeney ◽  
Kimberly Mueller ◽  
...  

Abstract. Greenhouse gas emissions mitigation requires understanding the dominant processes controlling fluxes of these trace gases at increasingly finer spatial and temporal scales. Trace gas fluxes can be estimated using a variety of approaches that translate observed atmospheric species mole fractions into fluxes or emission rates, often identifying the spatial and temporal characteristics of the emission sources as well. Meteorological models are commonly combined with tracer dispersion models to estimate fluxes using an inverse approach that optimizes emissions to best fit the trace gas mole fraction observations. One way to evaluate the accuracy of atmospheric flux estimation methods is to compare results from independent methods, including approaches in which different meteorological and tracer dispersion models are used. In this work, we use a rich data set of atmospheric methane observations collected during an intensive airborne campaign to compare different methane emissions estimates from the Barnett Shale oil and natural gas production basin in Texas, USA. We estimate emissions based on a variety of different meteorological and dispersion models. Previous estimates of methane emissions from this region relied on a simple model (a mass balance analysis) as well as on ground-based measurements and statistical data analysis (an inventory). We find that in addition to meteorological model choice, the choice of tracer dispersion model also has a significant impact on the predicted downwind methane concentrations given the same emissions field. The dispersion models tested often underpredicted the observed methane enhancements with significant variability (up to a factor of 3) between different models and between different days. We examine possible causes for this result and find that the models differ in their simulation of vertical dispersion, indicating that additional work is needed to evaluate and improve vertical mixing in the tracer dispersion models commonly used in regional trace gas flux inversions.


2015 ◽  
Vol 49 (13) ◽  
pp. 7889-7895 ◽  
Author(s):  
Tara I. Yacovitch ◽  
Scott C. Herndon ◽  
Gabrielle Pétron ◽  
Jonathan Kofler ◽  
David Lyon ◽  
...  

2003 ◽  
Author(s):  
Mark Parker ◽  
Billy Slabaugh ◽  
Harold Walters ◽  
Thomas Hart ◽  
F. Howard Howard Walsh ◽  
...  

2020 ◽  
Vol 39 (4) ◽  
pp. 291-291

The March 2020 TLE article by Alexandrov et al., “Normal faulting activated by hydraulic fracturing: A case study from the Barnett Shale, Fort Worth Basin,” contained an error in the third author's affiliation and e-mail address. Umair bin Waheed's correct affiliation is King Fahd University of Petroleum and Minerals, and the correct e-mail address for the author is [email protected] .


2003 ◽  
Vol 3 (1) ◽  
pp. 73-88 ◽  
Author(s):  
F. Dentener ◽  
M. van Weele ◽  
M. Krol ◽  
S. Houweling ◽  
P. van Velthoven

Abstract. The trend and interannual variability of methane sources are derived from multi-annual simulations of tropospheric photochemistry using a 3-D global chemistry-transport model. Our semi-inverse analysis uses the fifteen years (1979--1993) re-analysis of ECMWF meteorological data and annually varying emissions including photo-chemistry, in conjunction with observed CH4 concentration distributions and trends derived from the NOAA-CMDL surface stations. Dividing the world in four zonal regions (45--90 N, 0--45 N, 0--45 S, 45--90 S) we find good agreement in each region between (top-down) calculated emission trends from model simulations and (bottom-up) estimated anthropogenic emission trends based on the EDGAR global anthropogenic emission database, which amounts for the period 1979--1993 2.7 Tg CH4 yr-1. Also the top-down determined total global methane emission compares well with the total of the bottom-up estimates. We use the difference between the bottom-up and top-down determined emission trends to calculate residual emissions. These residual emissions represent the inter-annual variability of the methane emissions. Simulations have been performed in which the year-to-year meteorology, the emissions of ozone precursor gases, and the stratospheric ozone column distribution are either varied, or kept constant. In studies of methane trends it is most important to include the trends and variability of the oxidant fields. The analyses reveals that the variability of the emissions is of the order of 8Tg CH4 yr-1, and likely related to wetland emissions and/or biomass burning.


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