Environmental Indicators: Ozone Depletion
Technical SupplementThis technical appendix contains:
In addition to the format below, the entire Technical Supplement is available in Adobe Acrobat (PDF) format. It is a 139K file called techsupp.pdf. For additional information, please contact the
contacts for each chart or Ms. Susan Auby, Mail Code
2152, Office of Environmental Information, USEPA, 1200
Pennsylvania Avenue, NW, Washington, DC 20460. Phone
(202) 260-4901, e-mail:
auby.susan@epa.gov.
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U.S. Impact on the Ozone layer |
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DATA SOURCEU.S. production data for chlorofluorocarbons CFC-11
and CFC-12 come from the United States International
Trade Commission,
Synthetic Organic Chemicals; United States Production
and Sales, 1993, Table 3-1, p. 3-21 (Washington, DC:
GPO, 1994), and from earlier annual reports in this
series. Annual production data are summed and cumulative
totals calculated for years 1958 through 1993.
World production data for CFC-11 and CFC-12 come from
the Alternative Fluorocarbons Environmental Acceptability
Study (AFEAS),
Production, Sales and Atmospheric Release of
Fluorocarbons Through 1993, Data Tables 2 and 3
(Washington, DC: AFEAS, 1995). Annual production data are
reported by participating companies to an independent
accountant. Production data are summed and reported for
years 1958 through 1993 for the purpose of this bulletin.
U.S. cumulative totals (ITC) are subtracted from AFEAS
world totals to calculate "rest of the world" totals.
DATA COLLECTED AND PURPOSEThe U.S. International Trade Commission reports
annually on domestic production and sales of synthetic
organic chemicals and the raw materials from which they
are made. The report is prepared under investigation No.
332-135, Synthetic Organic Chemical Reports. This
investigation is conducted under the authority of section
332(g) of the Tariff Act of 1930 (19 U.S.C. 1322(g)), for
the purpose of collecting data and preparing public
reports on synthetic organic chemicals, plastics
materials, medicinal chemicals, pesticides, and other
chemical products. The data are collected by survey of
chemical manufacturers and include the total output of
each company's plants, i.e., the quantities produced for
consumption within the producing plant, as well as the
quantities produced for domestic and foreign sales.
Statistics for an individual chemical or group of
chemicals are given only when there are three or more
producers, no one or two of which may be predominant, and
when their publication would not violate the statutory
provisions relating to unlawful disclosure of information
accepted in confidence by the Commission.
GEOGRAPHICAL COVERAGEIn the AFEAS survey, global production of CFCs reflects production by plants in the following countries: Argentina, Australia, Brazil, Canada, the European Union, Japan, Mexico, South America, the United States, and Venezuela. It has been estimated that the data collected for 1993 represents probably less than 75 percent of worldwide production for dispersive uses. Coverage varies from year to year since 1982, as shown in the following table. For years prior to 1982, 100 percent coverage is assumed. U.S. production reported to ITC is the total quantity of a commodity made available by original manufacturers located within the customs territory of the United States (including the 50 states, the District of Columbia, and Puerto Rico). Table 1: World coverage of CFC-11 and CFC-12 production data, 1982-1993
DATA COLLECTION PERIODFor CFC-12, there is an unbroken time series for world production since 1931 and for U.S. production since 1958. For CFC-11, there is an unbroken time series for world production since 1934 and for U.S. production since 1958. Prior to 1958, total cumulative production of CFC-11 and CFC-12 was less than 750 thousand metric tons. For graphical purposes, only data from 1958 forward are displayed. METHOD AND FREQUENCY OF DATA COLLECTIONData contained in the ITC annual report are compiled primarily from the Commission's questionnaires sent to domestic chemical producers (643 companies for the 1993 annual report). Data are collected annually.Data contained in the AFEAS annual report are compiled from questionnaires solicited by the Alternative Fluorocarbons Environmental Acceptability Study and submitted by chemical manufacturers. A listing of all the companies surveyed inclusive of any related subsidiaries and/or joint ventures that may have reported data is contained in each annual report. Sales are divided into use categories, such as refrigeration, foam blowing, aerosols, solvents, and other uses. Some degree of geographical breakdown is also provided. In addition, calculations of atmospheric release of fluorocarbons, based on the survey data, are made. Further detail of data collection and emission estimation procedures and associated uncertainties, and the geographical distribution of emissions has been published (see References below). DATA PRESENTATIONThe data for the indicator (Figure 2) which are listed in Table 2 show the total cumulative production of CFC-11 and CFC-12 for the United States and the rest of the world from 1958 through 1993. See the table above for percent of world coverage in a given year. ITC reports production data in kilograms and AFEAS reports in metric tons. For this bulletin, data were converted to metric tons.
Table 2: Cumulative production of CFC-11 and
CFC-12 for the United States and the rest of the world,
1958-1993
Source: ITC and AFEAS, with world coverage factors applied to AFEAS data. REFERENCESAlternative Fluorocarbons Environmental Acceptability Study, Production, Sales and Atmospheric Release of Fluorocarbons through 1993 (Washington, DC: AFEAS, 1995). Note: This report was published annually by the Chemical Manufacturers Association until 1991. Since 1992, it has been published by the Alternative Fluorocarbons Environmental Acceptability Study. Gamlen, P.H., B.C. Lane, and P.M. Midgely, The Production and Release to the Atmosphere of CCl 3F and CCl 2F 2 (Chlorofluorocarbons CFC-11 and CFC-12). Atmospheric Environment, 20: 1107-1085 (1986). McCarthy, R.L., F.A. Bower, and J.P. Jenson, The Fluorocarbon-Ozone Theory - I. Production and Release: World Production and Release of CCl 3F and CCl 2F 2 (Fluorocarbons 11 and 12) Through 1975. Atmospheric Environment, 11: 491-497 (1977). United States International Trade Commission (ITC),
Synthetic Organic Chemicals; United States Production
and Sales, 1993, Table 3-1, pp. 3-19 and 3-21
(Washington, DC: GPO, 1994), and from earlier annual
reports in this series.
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Indicator:
Atmospheric Concentration of Selected Ozone-Depleting Chemicals |
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DATA SOURCEMeasurements of the atmospheric concentrations of selected ozone-depleting chemicals come from the Atmospheric Lifetime Experiment (ALE)/Global Atmospheric Gases Experiment (GAGE)/Advanced GAGE network. Contact Person for Atmospheric Concentrations of
Selected Ozone-Depleting Chemicals:
For information about CDIAC numeric data packages and
select data bases, contact:
DATA COLLECTED AND PURPOSEIn the ALE/GAGE/AGAGE global network program, continuous high frequency gas chromatographic measurements of two biogenic/anthropogenic gases (methane and nitrous oxide) and five anthropogenic gases [chlorofluorocarbons CFCl 3 (CFC-11), CF 2Cl 2 (CFC-12), and CF 2ClCFCl 2 (CFC-113); methyl chloroform, CH 3CCL 3; and carbon tetrachloride, CCl4] are carried out at four globally-distributed sites: Cape Grim, Tasmania; Point Matatula, American Samoa; Ragged Point, Barbados; and Mace Head, Ireland. Stations also previously existed at Cape Meares, Oregon, and at Adrigole, Ireland. The program, which began in 1978, is designed to accurately determine the atmospheric concentrations and long-term trends of these important trace gases so that their global circulation rates and globally averaged atmospheric lifetimes can be calculated. The Cape Grim, Tasmania station was selected as the source of data for this indicator as it is both representative and has the longest time series for the complete ALE/GAGE schedule of trace gases. GEOGRAPHICAL COVERAGEGlobal. The Cape Grim data are shown. DATA COLLECTION PERIODData for CFC-11, CFC-12, and nitrous oxide have been collected fairly continuously at each station since July 1978. Beginning in late 1983 at Cape Grim and later at the other sites, the additional measurements were added to the program. By mid-1986, ALE had ended and was succeeded by GAGE at all sites except the Adrigole (Ireland) station, which closed in December 1983 and was replaced by the GAGE station at Mace Head in January 1987. METHOD AND FREQUENCY OF DATA COLLECTIONAir samples, collected 4 times daily for ALE and 12 times daily for GAGE, are filtered, dried, and analyzed using Hewlett Packard HP5840A (ALE) or HP5880A (GAGE) electron capture gas chromatographs. The recently initiated Advanced GAGE (AGAGE) uses a custom-designed sample module and HP5890 and Carle Instruments gas chromatographic components. DATA PRESENTATIONThe data from Cape Grim used for the indicator (Figure 3), which are listed in Table 3, show monthly mean halocarbon mixing ratios expressed as parts per trillion by volume. The principal investigators calculated monthly mixing ratios by averaging individual measurements (after removing pollution events). Data are available, in principle, from measurements taken four-times daily for ALE from July 1978 through June 1985 and 12 times-daily for GAGE from December 1981 through June 1994. For CFC-11, individual measurements actually represent averages of the separate measurements made on two different chromatographic columns when both values are available. For the graphical presentation of the data, in the bulletin gaps caused by missing monthly values were filled with averages.
Table 3: Atmospheric concentrations of selected
ozone-depleting chemicals, 1978-1994
CFC-11 (GAGE)
Table 3: Atmospheric concentrations of selected
ozone-depleting chemicals, 1978-1994 (continued)
CFC-12 (GAGE)
Table 3: Atmospheric concentrations of selected
ozone-depleting chemicals, 1978-1994 (continued)
CH 3CCl 3 (GAGE)
Table 3: Atmospheric concentrations of selected
ozone-depleting chemicals, 1978-1994 (continued)
CCl 4 (GAGE)
Source: Prinn, et al. (1994) and recent updates to database. See References. REFERENCESCunnold, D.M., P.J. Fraser, R.F. Weiss, R.G. Prinn, P.G. Simmonds, F.N. Alyea, and A.J. Crawford. Global trends and annual releases of CCl 3F and CCl 2F 2 estimated from ALE/GAGE and other measurements for July 1978 to June 1991. J. Geophys. Res. 99(D1):1107-1126 (January 1994). Prinn, R.G., P.G. Simmonds, R.A. Rasmussen, R.D. Rosen, F.N. Alyea, C.A. Cardelino, A.J. Crawford, D.M. Cunnold, P.J. Fraser, and J.E. Lovelock. The Atmospheric Lifetime Experiment. 1. Introduction, instrumentation and overview. J. Geophys. Res. 88 (C13):8353-8367 (January 1983). Prinn, R.G., D.M. Cunnold, R.A. Rasmussen, P.G. Simmonds, F.N. Alyea, A.J. Crawford, P.J. Fraser, and R.D. Rosen. Atmospheric emissions and trends of nitrous oxide deduced from 10 years of ALE-GAGE data. J. Geophys. Res. 95(D11):18369-18385 (October 1990). Prinn, R.G., D.M. Cunnold, P.G. Simmonds, F.N. Alyea, R. Boldi, A.J. Crawford, P.J. Fraser, D. Gutzler, D. Hartley, R. Rosen, and R.A. Rasmussen. Global average concentration and trend for hydroxyl radicals deduced from ALE/GAGE trichloroethane (methyl chloroform) data for 1978-1990. J. Geophys. Res. 97(D2):2445-2461 (February 1992). Prinn, R.G., R.F. Weiss, F.N. Alyea, D.M. Cunnold, P.J. Fraser, P.G. Simmonds, A.J. Crawford, R.A. Rasmussen, and R.D. Rosen. 1994. "Atmospheric CFC-11 (CCL3F), CFC-12 (CCL2F2), and N2O from the ALE-GAGE network," pp. 396-420 . In T.A. Boden, D.P. Kaiser, R.J. Sepanski, and F.W. Stoss (eds.), Trends '93: A Compendium of Data on Global Change. ORNL/CDIAC-65. Carbon Dioxide Information Analysis Center, Oak Ridge National Laboratory, Oak Ridge, TN, U.S.A. Prinn, R.G., R.F. Weiss, B.R. Miller, J. Huang, F.N. Alyea, D.M. Cunnold, P.B. Fraser, D.E. Hartley, and P.G. Simmonds. Atmospheric trends and lifetime of Trichloroethane and global hydroxyl radical concentrations. Accepted for publication in Science (May, 1995). Simmonds, P., D. Cunnold, F. Alyea, C. Cardelino, A.
Crawford, P. Fraser, R. Prinn, R. Rasmussen, and R.
Rosen. Carbon tetrachloride lifetime and emissions
determined from global daily measurements during
1978-1985.
J. Atmos. Chem. 7: 35-58 (1988).
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Indicator:
Ozone Depletion Over Antarctica |
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Ozone Depletion Over Antarctica, Mean October Values at Halley Station, Graph 1
DATA SOURCEBritish Antarctic Survey (BAS)
DATA COLLECTED AND PURPOSEData are collected using the Dobson ozone spectrophotometer. Some experimental zenith observations at low solar elevation are included in data beginning in April 1993. GEOGRAPHICAL COVERAGEThe Dobson ozone spectrophotometer is at the Halley Research Station, located at 75°35’ South and 26°34’ West on the Brunts Ice Shelf in Coats Land, Antarctica. DATA COLLECTION PERIODThe data collection period is from 1956 through 2002. METHODOLOGY AND FREQUENCY OF DATA COLLECTIONData are collected with a Dobson ozone spectrophotometer at the Halley Station in Antarctica. 1987/88 data include ozonesonde flight results. Data are approximately corrected to Bass-Paur ozone absorption coefficients. DATA PRESENTATIONData are expressed in Dobson units for the time period 1956 through 2002. Table 4: Ozone Depletion Over Antarctica, Mean October Values, 1956-2002
REFERENCESNatural Environment Research Council, British Antarctic Survey. 2002. “Halley Research Station.” http://www.antarctica.ac.uk/Living_and_Working/Stations/Halley/index.php. Accessed 5/30/03. Natural Environment Research Council, British Antarctic Survey. 2003. “British Antarctic Survey Ozone Halley, Rothera, and Vernadsky/Faraday.” http://www.antarctica.ac.uk/met/jds/ozone/. Accessed 5/30/03. Shanklin, J.D. British Antarctic Survey, Madingley Road, Cambridge, England. CB3 0ET. “Provisional monthly mean ozone values for Faraday/Vernadsky and Halley between 1956 and 2002.” http://www.antarctica.ac.uk/met/jds/ozone/data/zoz5699.dat. Accessed 5/30/03. |
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Indicator:
Impact of Montreal Protocol on Chlorine Content of the Atmosphere |
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DATA SOURCEInformation extracted from industry reports was used as input to a model that generates estimates of chlorine loading to the stratosphere. Industry reports are on file at the U.S. Environmental Protection Agency. Contact Person for Information on Chlorine Loading to the Stratosphere :Erin Birgfeld U.S. Environmental Protection Agency (EPA) Office of Air and Radiation Global Programs Division Mail Code 6205J 1200 Pennsylvania Avenue, NW Washington, DC 20460 Telephone: (202) 564-9079 Email: birgfeld.erin@epa.gov DATA COLLECTED AND PURPOSEData on chlorine loading were not collected, but were generated by a model, based on reported information. GEOGRAPHICAL COVERAGEGlobal. DATA COLLECTION PERIODModel-generated estimates based on reported data are from 1985 through 1991. Later estimates are model-generated forecasts are based on assumptions to 2030. METHODOLOGY AND FREQUENCY OF DATA COLLECTIONData were not collected, but generated by the Atmospheric Stabilization Framework (ASF), a model developed during a 1988 workshop sponsored by NASA and EPA. The ASF is documented at NASA. The ASF is not a physical simulation. Rather, it is a parameterized model based on more complicated simulations and calibrated to meet historical measurements of ozone depletion in 1985 and 1989. DATA PRESENTATIONThe data for the indicator (Figure 5), which are listed in Table 5, show adjusted atmospheric chlorine loading in parts per billion (ppb) for the time period 1985 to 2030. One scenario assumes no controls to limit chlorine loading and the other scenario assumes the phaseout of production and consumption of ozone-depleting chemicals in accordance with the Montreal Protocol on Substances that Deplete the Ozone Layer (which entered into force in 1989).
Table 5: Adjusted atmospheric chlorine loading,
1985-2030
REFERENCESNational Aeronautics and Space Administration (NASA), Goddard Space Flight Center (GSFC). An Assessment Model for Atmospheric Composition. NASA Conference Publication 3203 (94N17827) (Greenbelt, MD: NASA/GSFC, 1988). TERMINOLOGYA chlorofluorocarbon is one of a group of organic chemicals containing carbon, fluorine and chlorine. CFCs have been used as coolants in refrigerators and air conditioners and as foaming agents, solvents, and aerosol propellants. Chlorofluorocarbons discussed in this technical supplement include CFC-11 (Trichlorofluoromethane), CFC-12 (Dichlorodifluoromethane), CFC-113 (Trichlorotrifluoroethane), and HCFC-22 (Chlorodifluoromethane). Carbon tetrachloride is an industrial solvent. It is largely used in the manufacture of chlorofluorocarbons and similar chemicals. A Dobson unit is a unit of measure used to estimate the thickness of the ozone layer. One hundred (100) Dobson units represent a quantity equivalent to a 1 mm thick layer of ozone at sea level. Hydrochlorofluorocarbons contain hydrogen, in addition to carbon, chlorine and fluorine. HCFCs have many of the same uses as CFCs and are increasingly used as interim substitutes for CFCs. HCFCs retain many of the desirable properties of CFCs but because they exist for a shorter time in the atmosphere, ozone depletion and global warming concerns are significantly reduced.
Irradiance refers to solar light that is
reflected in the atmosphere.
Links to Other InformationOzone Depletion ScienceOzone Monitoring UV Index and UV Monitoring Health Effects of Ozone Depletion |
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