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      Continued Emissions of the Ozone-Depleting Substance Carbon Tetrachloride From Eastern Asia

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          Abstract

          Carbon tetrachloride (CCl 4) is an ozone-depleting substance, accounting for about 10% of the chlorine in the troposphere. Under the terms of the Montreal Protocol, its production for dispersive uses was banned from 2010. In this work we show that, despite the controls on production being introduced, CCl 4 emissions from the eastern part of China did not decline between 2009 and 2016. This finding is in contrast to a recent bottom-up estimate, which predicted a significant decrease in emissions after the introduction of production controls. We find eastern Asian emissions of CCl 4 to be 16 (9–24) Gg/year on average between 2009 and 2016, with the primary source regions being in eastern China. The spatial distribution of emissions that we derive suggests that the source distribution of CCl 4 in China changed during the 8-year study period, indicating a new source or sources of emissions from China’s Shandong province after 2012.

          Plain Language Summary

          Carbon tetrachloride is one of several man-made gases that contribute to the depletion of the ozone layer high in the atmosphere. Because of this, restrictions were introduced on the use of this ozone-depleting substance, with the expectation that production should by now be close to 0. However, the slower than expected rate of decline of carbon tetrachloride in the atmosphere shows this is not the case, and a large portion of global emissions are unaccounted for. In this study we use atmospheric measurements of carbon tetrachloride from a site in East Asia to identify the magnitude and location of emissions from this region between 2009 and 2016. We find that there are significant ongoing emissions from eastern China and that these account for a large part of the missing emissions from global estimates. The presence of continued sources of this important ozone-depleting substance indicates that more could be done to speed up the recovery of the ozone layer.

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          Most cited references38

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          Inverse Problem Theory and Methods for Model Parameter Estimation

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            An unexpected and persistent increase in global emissions of ozone-depleting CFC-11

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              Description of the analysis of a wide range of volatile organic compounds in whole air samples collected during PEM-tropics A and B.

              A large number of hydrocarbons, halocarbons, and organic nitrates were quantified in whole air samples acquired for the NASA-sponsored GTE missions PEM-Tropics A and B. The samples were collected in electro-polished stainless steel canisters from two aircraft while flying over the Pacific Basin. Two nominally identical multicolumn multidetector gas chromatographic analytical systems were employed. Whole air samples were also used as working and calibrated standards and were collected specifically for this purpose. This paper describes the analytical procedure employed during PEM-Tropics B. Minor differences in the PEM-Tropics A system will also be discussed. More than 3,900 samples were analyzed for 34 gases during PEM-Tropics A, over 4,500 samples were analyzed for 58 gases during PEM-Tropics B. An overview is presented of the collection, analysis, and quantification of whole air samples during the PEM-Tropics missions, along with an analysis of the analytical precision achieved during these missions.
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                Author and article information

                Journal
                9882887
                22888
                Geophys Res Lett
                Geophys Res Lett
                Geophysical research letters
                0094-8276
                1944-8007
                3 September 2020
                28 September 2018
                28 October 2018
                30 September 2020
                : 45
                : 20
                : 11423-11430
                Affiliations
                [1 ]School of Chemistry, University of Bristol, Bristol, UK
                [2 ]Kyungpook Institute of Oceanography, College of Natural Sciences, Kyungpook National University, Daegu, South Korea
                [3 ]Department of Oceanography, School of Earth System Sciences, Kyungpook National University, Daegu, South Korea
                [4 ]Empa, Swiss Federal Laboratories for Materials Science and Technology, Dübendorf, Switzerland
                [5 ]Hadley Centre, UK Met Office, Exeter, UK
                [6 ]School of Geographical Sciences, University of Bristol, Bristol, UK
                [7 ]Department of Chemistry, University of California, Irvine, CA, USA
                [8 ]Atmospheric Chemistry and Dynamics, NASA Goddard Space Flight Center, Greenbelt, MD, USA
                [9 ]Scripps Institution of Oceanography, University of California, San Diego, La Jolla, CA, USA
                [10 ]Climate Science Centre, CSIRO Oceans and Atmosphere, Aspendale, Victoria, Australia
                [11 ]Center for Global Change Science, Massachusetts Institute of Technology, Cambridge, MA, USA
                Author notes
                Correspondence to: M. F. Lunt and M. Rigby, Mark.Lunt@ 123456bristol.ac.uk ; matt.rigby@ 123456bristol.ac.uk
                Author information
                http://orcid.org/0000-0002-0827-2137
                http://orcid.org/0000-0002-6637-4887
                http://orcid.org/0000-0002-1431-7514
                http://orcid.org/0000-0001-5715-8923
                http://orcid.org/0000-0002-4211-1126
                http://orcid.org/0000-0002-8283-5014
                http://orcid.org/0000-0002-8430-0515
                http://orcid.org/0000-0002-4051-6760
                http://orcid.org/0000-0001-9776-3642
                http://orcid.org/0000-0001-9551-7739
                http://orcid.org/0000-0002-4884-3678
                http://orcid.org/0000-0001-5925-3801
                http://orcid.org/0000-0002-9885-7138
                http://orcid.org/0000-0002-2020-9253
                Article
                NASAPA1517285
                10.1029/2018gl079500
                7526663
                33005064
                2a777792-21dd-42d1-a0dc-7c52564b475b

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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