Science.gov

Sample records for 8-hour average ozone

  1. 40 CFR 51.908 - What modeling and attainment demonstration requirements apply for purposes of the 8-hour ozone...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... demonstration requirements apply for purposes of the 8-hour ozone NAAQS? 51.908 Section 51.908 Protection of..., AND SUBMITTAL OF IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient... purposes of the 8-hour ozone NAAQS? (a) What is the attainment demonstration requirement for an...

  2. 40 CFR 51.908 - What modeling and attainment demonstration requirements apply for purposes of the 8-hour ozone...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... demonstration requirements apply for purposes of the 8-hour ozone NAAQS? 51.908 Section 51.908 Protection of..., AND SUBMITTAL OF IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient... purposes of the 8-hour ozone NAAQS? (a) What is the attainment demonstration requirement for an...

  3. 40 CFR 51.908 - What modeling and attainment demonstration requirements apply for purposes of the 8-hour ozone...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... demonstration requirements apply for purposes of the 8-hour ozone NAAQS? 51.908 Section 51.908 Protection of..., AND SUBMITTAL OF IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient... purposes of the 8-hour ozone NAAQS? (a) What is the attainment demonstration requirement for an...

  4. 40 CFR 51.908 - What modeling and attainment demonstration requirements apply for purposes of the 8-hour ozone...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... demonstration requirements apply for purposes of the 8-hour ozone NAAQS? 51.908 Section 51.908 Protection of..., AND SUBMITTAL OF IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient... purposes of the 8-hour ozone NAAQS? (a) What is the attainment demonstration requirement for an...

  5. 40 CFR 51.914 - What new source review requirements apply for 8-hour ozone nonattainment areas?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... apply for 8-hour ozone nonattainment areas? 51.914 Section 51.914 Protection of Environment... Standard § 51.914 What new source review requirements apply for 8-hour ozone nonattainment areas? The requirements for new source review for the 8-hour ozone standard are located in § 51.165 of this part....

  6. 40 CFR 51.914 - What new source review requirements apply for 8-hour ozone nonattainment areas?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... apply for 8-hour ozone nonattainment areas? 51.914 Section 51.914 Protection of Environment... Standard § 51.914 What new source review requirements apply for 8-hour ozone nonattainment areas? The requirements for new source review for the 8-hour ozone standard are located in § 51.165 of this part....

  7. 40 CFR 51.914 - What new source review requirements apply for 8-hour ozone nonattainment areas?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... apply for 8-hour ozone nonattainment areas? 51.914 Section 51.914 Protection of Environment... Standard § 51.914 What new source review requirements apply for 8-hour ozone nonattainment areas? The requirements for new source review for the 8-hour ozone standard are located in § 51.165 of this part....

  8. 40 CFR 51.914 - What new source review requirements apply for 8-hour ozone nonattainment areas?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... apply for 8-hour ozone nonattainment areas? 51.914 Section 51.914 Protection of Environment... Standard § 51.914 What new source review requirements apply for 8-hour ozone nonattainment areas? The requirements for new source review for the 8-hour ozone standard are located in § 51.165 of this part....

  9. 40 CFR 51.914 - What new source review requirements apply for 8-hour ozone nonattainment areas?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... apply for 8-hour ozone nonattainment areas? 51.914 Section 51.914 Protection of Environment... Standard § 51.914 What new source review requirements apply for 8-hour ozone nonattainment areas? The requirements for new source review for the 8-hour ozone standard are located in § 51.165 of this part....

  10. 76 FR 54412 - Determination of Nonattainment and Reclassification of the Baltimore 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-01

    ... Part 81 Air pollution control, National parks, Wilderness areas. Authority: 42 U.S.C. 7401 et seq... Baltimore Area) did not attain the 1997 8-hour ozone national ambient air quality standard (NAAQS) by its... Agency, Region III, 1650 Arch Street, Philadelphia, Pennsylvania 19103. D. Hand Delivery: At...

  11. 40 CFR 51.916 - What are the requirements for an Ozone Transport Region under the 8-hour NAAQS?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 2 2010-07-01 2010-07-01 false What are the requirements for an Ozone... IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.916 What are the requirements for an Ozone Transport Region under the 8-hour NAAQS? (a) In...

  12. 40 CFR 50.10 - National 8-hour primary and secondary ambient air quality standards for ozone.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... ambient air quality standards for ozone. 50.10 Section 50.10 Protection of Environment ENVIRONMENTAL....10 National 8-hour primary and secondary ambient air quality standards for ozone. (a) The level of the national 8-hour primary and secondary ambient air quality standards for ozone, measured by...

  13. 40 CFR 52.387 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-hour ozone and PM2.5 NAAQS. 52.387 Section 52.387 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.387 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On March 13, 2007, the State...)(D)(i) interstate transport requirements of the Clean Air Act for the 1997 8-hour ozone and...

  14. 40 CFR 51.916 - What are the requirements for an Ozone Transport Region under the 8-hour NAAQS?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 2 2014-07-01 2014-07-01 false What are the requirements for an Ozone... IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.916 What are the requirements for an Ozone Transport Region under the 8-hour NAAQS? (a) In...

  15. 40 CFR 51.916 - What are the requirements for an Ozone Transport Region under the 8-hour NAAQS?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 2 2012-07-01 2012-07-01 false What are the requirements for an Ozone... IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.916 What are the requirements for an Ozone Transport Region under the 8-hour NAAQS? (a) In...

  16. 40 CFR 52.387 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-hour ozone and PM2.5 NAAQS. 52.387 Section 52.387 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.387 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On March 13, 2007, the State...)(D)(i) interstate transport requirements of the Clean Air Act for the 1997 8-hour ozone and...

  17. 40 CFR 51.916 - What are the requirements for an Ozone Transport Region under the 8-hour NAAQS?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 2 2011-07-01 2011-07-01 false What are the requirements for an Ozone... IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.916 What are the requirements for an Ozone Transport Region under the 8-hour NAAQS? (a) In...

  18. 40 CFR 52.387 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...-hour ozone and PM2.5 NAAQS. 52.387 Section 52.387 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.387 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On March 13, 2007, the State...)(D)(i) interstate transport requirements of the Clean Air Act for the 1997 8-hour ozone and...

  19. 40 CFR 52.387 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...-hour ozone and PM2.5 NAAQS. 52.387 Section 52.387 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.387 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On March 13, 2007, the State...)(D)(i) interstate transport requirements of the Clean Air Act for the 1997 8-hour ozone and...

  20. 40 CFR 50.10 - National 8-hour primary and secondary ambient air quality standards for ozone.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... ambient air quality standards for ozone. 50.10 Section 50.10 Protection of Environment ENVIRONMENTAL....10 National 8-hour primary and secondary ambient air quality standards for ozone. (a) The level of the national 8-hour primary and secondary ambient air quality standards for ozone, measured by...

  1. 40 CFR 51.916 - What are the requirements for an Ozone Transport Region under the 8-hour NAAQS?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 2 2013-07-01 2013-07-01 false What are the requirements for an Ozone... IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.916 What are the requirements for an Ozone Transport Region under the 8-hour NAAQS? (a) In...

  2. 40 CFR 52.387 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-hour ozone and PM2.5 NAAQS. 52.387 Section 52.387 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.387 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On March 13, 2007, the State...)(D)(i) interstate transport requirements of the Clean Air Act for the 1997 8-hour ozone and...

  3. 40 CFR 52.1393 - Interstate Transport Declaration for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... the 1997 8-hour ozone and PM2.5 NAAQS. 52.1393 Section 52.1393 Protection of Environment ENVIRONMENTAL... (CONTINUED) Montana § 52.1393 Interstate Transport Declaration for the 1997 8-hour ozone and PM2.5 NAAQS. The... Section 110(a)(2)(D)(i) for the 8-hour ozone and PM2.5 NAAQS promulgated in July 1997. The...

  4. 40 CFR 52.1393 - Interstate Transport Declaration for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... the 1997 8-hour ozone and PM2.5 NAAQS. 52.1393 Section 52.1393 Protection of Environment ENVIRONMENTAL... (CONTINUED) Montana § 52.1393 Interstate Transport Declaration for the 1997 8-hour ozone and PM2.5 NAAQS. The... Section 110(a)(2)(D)(i) for the 8-hour ozone and PM2.5 NAAQS promulgated in July 1997. The...

  5. 40 CFR 52.1393 - Interstate Transport Declaration for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... the 1997 8-hour ozone and PM2.5 NAAQS. 52.1393 Section 52.1393 Protection of Environment ENVIRONMENTAL... (CONTINUED) Montana § 52.1393 Interstate Transport Declaration for the 1997 8-hour ozone and PM2.5 NAAQS. The... Section 110(a)(2)(D)(i) for the 8-hour ozone and PM2.5 NAAQS promulgated in July 1997. The...

  6. 40 CFR 52.1393 - Interstate Transport Declaration for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... the 1997 8-hour ozone and PM2.5 NAAQS. 52.1393 Section 52.1393 Protection of Environment ENVIRONMENTAL... (CONTINUED) Montana § 52.1393 Interstate Transport Declaration for the 1997 8-hour ozone and PM2.5 NAAQS. The... Section 110(a)(2)(D)(i) for the 8-hour ozone and PM2.5 NAAQS promulgated in July 1997. The...

  7. 40 CFR 52.2499 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. 52.2499 Section 52.2499 Protection of Environment ENVIRONMENTAL PROTECTION...) Washington § 52.2499 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On January 17, 2007,...

  8. 40 CFR 52.97 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. 52.97 Section 52.97 Protection of Environment ENVIRONMENTAL PROTECTION....97 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On February 7, 2008, the...

  9. 40 CFR 52.97 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. 52.97 Section 52.97 Protection of Environment ENVIRONMENTAL PROTECTION....97 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On February 7, 2008, the...

  10. 40 CFR 52.97 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. 52.97 Section 52.97 Protection of Environment ENVIRONMENTAL PROTECTION....97 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On February 7, 2008, the...

  11. 40 CFR 52.2499 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. 52.2499 Section 52.2499 Protection of Environment ENVIRONMENTAL PROTECTION...) Washington § 52.2499 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On January 17, 2007,...

  12. 40 CFR 52.97 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. 52.97 Section 52.97 Protection of Environment ENVIRONMENTAL PROTECTION....97 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On February 7, 2008, the...

  13. 40 CFR 52.2499 - Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. 52.2499 Section 52.2499 Protection of Environment ENVIRONMENTAL PROTECTION...) Washington § 52.2499 Interstate Transport for the 1997 8-hour ozone and PM2.5 NAAQS. On January 17, 2007,...

  14. 40 CFR 50.10 - National 8-hour primary and secondary ambient air quality standards for ozone.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... ozone NAAQS are codified in 40 CFR part 81. ... ambient air quality standards for ozone. 50.10 Section 50.10 Protection of Environment ENVIRONMENTAL....10 National 8-hour primary and secondary ambient air quality standards for ozone. (a) The level...

  15. 40 CFR 50.10 - National 8-hour primary and secondary ambient air quality standards for ozone.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... with respect to the 1997 ozone NAAQS are codified in 40 CFR part 81. ... ambient air quality standards for ozone. 50.10 Section 50.10 Protection of Environment ENVIRONMENTAL....10 National 8-hour primary and secondary ambient air quality standards for ozone. (a) The level...

  16. 40 CFR 50.10 - National 8-hour primary and secondary ambient air quality standards for ozone.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... with respect to the 1997 ozone NAAQS are codified in 40 CFR part 81. ... ambient air quality standards for ozone. 50.10 Section 50.10 Protection of Environment ENVIRONMENTAL....10 National 8-hour primary and secondary ambient air quality standards for ozone. (a) The level...

  17. 75 FR 79302 - Determination of Nonattainment and Reclassification of the Dallas/Fort Worth 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-20

    ...-Hour Ozone Nonattainment Area; Texas AGENCY: Environmental Protection Agency (EPA). ACTION: Final rule... nonattainment area failed to attain the 1997 8-hour ozone national ambient air quality standard (NAAQS or... Federal Regulations (CFR) for moderate nonattainment areas. This final determination is based on...

  18. 40 CFR 51.918 - Can any SIP planning requirements be suspended in 8-hour ozone nonattainment areas that have air...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... suspended in 8-hour ozone nonattainment areas that have air quality data that meets the NAAQS? 51.918... 8-hour Ozone National Ambient Air Quality Standard § 51.918 Can any SIP planning requirements be suspended in 8-hour ozone nonattainment areas that have air quality data that meets the NAAQS? Upon...

  19. 40 CFR 51.918 - Can any SIP planning requirements be suspended in 8-hour ozone nonattainment areas that have air...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... suspended in 8-hour ozone nonattainment areas that have air quality data that meets the NAAQS? 51.918... 8-hour Ozone National Ambient Air Quality Standard § 51.918 Can any SIP planning requirements be suspended in 8-hour ozone nonattainment areas that have air quality data that meets the NAAQS? Upon...

  20. 40 CFR 51.918 - Can any SIP planning requirements be suspended in 8-hour ozone nonattainment areas that have air...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... suspended in 8-hour ozone nonattainment areas that have air quality data that meets the NAAQS? 51.918... 8-hour Ozone National Ambient Air Quality Standard § 51.918 Can any SIP planning requirements be suspended in 8-hour ozone nonattainment areas that have air quality data that meets the NAAQS? Upon...

  1. 40 CFR 51.918 - Can any SIP planning requirements be suspended in 8-hour ozone nonattainment areas that have air...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... suspended in 8-hour ozone nonattainment areas that have air quality data that meets the NAAQS? 51.918... 8-hour Ozone National Ambient Air Quality Standard § 51.918 Can any SIP planning requirements be suspended in 8-hour ozone nonattainment areas that have air quality data that meets the NAAQS? Upon...

  2. 40 CFR 51.917 - What is the effective date of designation for the Las Vegas, NV, 8-hour ozone nonattainment area?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... designation for the Las Vegas, NV, 8-hour ozone nonattainment area? 51.917 Section 51.917 Protection of... Air Quality Standard § 51.917 What is the effective date of designation for the Las Vegas, NV, 8-hour ozone nonattainment area? The Las Vegas, NV, 8-hour ozone nonattainment area (designated on September...

  3. 40 CFR 51.917 - What is the effective date of designation for the Las Vegas, NV, 8-hour ozone nonattainment area?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... designation for the Las Vegas, NV, 8-hour ozone nonattainment area? 51.917 Section 51.917 Protection of... Air Quality Standard § 51.917 What is the effective date of designation for the Las Vegas, NV, 8-hour ozone nonattainment area? The Las Vegas, NV, 8-hour ozone nonattainment area (designated on September...

  4. 40 CFR 51.917 - What is the effective date of designation for the Las Vegas, NV, 8-hour ozone nonattainment area?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... designation for the Las Vegas, NV, 8-hour ozone nonattainment area? 51.917 Section 51.917 Protection of... Air Quality Standard § 51.917 What is the effective date of designation for the Las Vegas, NV, 8-hour ozone nonattainment area? The Las Vegas, NV, 8-hour ozone nonattainment area (designated on September...

  5. 40 CFR 51.917 - What is the effective date of designation for the Las Vegas, NV, 8-hour ozone nonattainment area?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... designation for the Las Vegas, NV, 8-hour ozone nonattainment area? 51.917 Section 51.917 Protection of... Air Quality Standard § 51.917 What is the effective date of designation for the Las Vegas, NV, 8-hour ozone nonattainment area? The Las Vegas, NV, 8-hour ozone nonattainment area (designated on September...

  6. 40 CFR 51.917 - What is the effective date of designation for the Las Vegas, NV, 8-hour ozone nonattainment area?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... designation for the Las Vegas, NV, 8-hour ozone nonattainment area? 51.917 Section 51.917 Protection of... Air Quality Standard § 51.917 What is the effective date of designation for the Las Vegas, NV, 8-hour ozone nonattainment area? The Las Vegas, NV, 8-hour ozone nonattainment area (designated on September...

  7. 75 FR 57220 - Rule To Implement the 1997 8-Hour Ozone National Ambient Air Quality Standard: New Source Review...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-20

    ..., e-mail address, and telephone and fax numbers. Questions concerning the August 24, 2010 (75 FR 51960... holding the public hearing was published in the Federal Register on August 24, 2010 (75 FR 51960), and is... AGENCY 40 CFR Part 51 RIN 2060-AP30 Rule To Implement the 1997 8-Hour Ozone National Ambient Air...

  8. 77 FR 28423 - Final Rule To Implement the 1997 8-Hour Ozone National Ambient Air Quality Standard...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-05-14

    ... based.'' The process for making these adjustments is described at 69 FR 23863 et seq. (April 30, 2004... rulemaking (74 FR 2936). \\1\\ 74 FR 2936, January 16, 2009. III. This Action A. Classification of 8-Hour Ozone... Determination, pursuant to 40 CFR 51.918, 70 FR 71702). The obligation to complete and submit those...

  9. 75 FR 68733 - Approval and Promulgation of One-Year Extension for Attaining the 1997 8-Hour Ozone Standard for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-11-09

    ... for a 1-year extension, the Philadelphia Area's 4th highest daily 8-hour monitored ozone value during...), as required by 40 CFR 51.907(a). The highest-reading monitoring site had a 4th high value for 2009 of... Control Measure'' proposed July 22, 2010 (75 FR 42672); and (2) The maximum 4th highest daily...

  10. 76 FR 33647 - Approval and Promulgation of Determination of Attainment for the 1997 8-Hour Ozone Standard...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-06-09

    .... Louis (MO-IL) metropolitan nonattainment area on February 28, 2011 (76 FR 10815). A detailed discussion... that the area has attained the NAAQS during the 2008- 2010 monitoring period. On March 27, 2008 (73 FR... addressed this 2008 revised standard and proposed to set the primary 8-hour ozone standard within the...

  11. 76 FR 2859 - Approval and Promulgation of Air Quality Implementation Plans; Virginia; Adoption of 8-hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-18

    ... of 8-hour Ozone Standard and Related Reference Conditions, and Update of Appendices AGENCY... reference conditions, and updating the list of appendices under ``Documents Incorporated by Reference.'' In... Reference Conditions, and Update of Appendices,'' that is located in the ``Rules and Regulations''...

  12. 40 CFR 51.908 - What modeling and attainment demonstration requirements apply for purposes of the 8-hour ozone...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... classified as moderate or higher under subpart 2 pursuant to § 51.903? An area classified as moderate or... area subject only to subpart 1 in accordance with § 51.902(b)? An area subject to § 51.902(b) shall be... demonstration requirements apply for purposes of the 8-hour ozone NAAQS? 51.908 Section 51.908 Protection...

  13. 76 FR 10815 - Approval and Promulgation of Determination of Attainment for the 1997 8-Hour Ozone Standard...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-28

    ... 12898 (59 FR 7629, February 16, 1994). In addition, this proposed 8-hour ozone clean NAAQS data... that the area has attained the NAAQS during the 2008-2010 monitoring period. On March 27, 2008 (73 FR... by the Office of Management and Budget under Executive Order 12866 (58 FR 51735, October 4,...

  14. 76 FR 13289 - Approval of One-Year Extension for Attaining the 1997 8-Hour Ozone Standard in the Baltimore...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-11

    ...).) List of Subjects in 40 CFR Part 81 Environmental protection, Air pollution control, National parks... Baltimore nonattainment area, which is classified as moderate for the 1997 8-hour ozone National Ambient Air....S. Environmental Protection Agency, Region III, 1650 Arch Street, Philadelphia, Pennsylvania...

  15. 40 CFR 52.1989 - Interstate Transport for the 1997 8-hour ozone NAAQS and 1997 PM2.5 NAAQS.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Interstate Transport for the 1997 8-hour ozone NAAQS and 1997 PM2.5 NAAQS. 52.1989 Section 52.1989 Protection of Environment ENVIRONMENTAL... (CONTINUED) Oregon § 52.1989 Interstate Transport for the 1997 8-hour ozone NAAQS and 1997 PM2.5 NAAQS....

  16. 40 CFR 51.918 - Can any SIP planning requirements be suspended in 8-hour ozone nonattainment areas that have air...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... suspended in 8-hour ozone nonattainment areas that have air quality data that meets the NAAQS? 51.918 Section 51.918 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS... 8-hour Ozone National Ambient Air Quality Standard § 51.918 Can any SIP planning requirements...

  17. 78 FR 65877 - Approval and Promulgation of Implementation Plans; Atlanta, Georgia 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-11-04

    ... noted, EPA has already approved Rule (jjj). See 64 FR 67491 and 74 FR 62249. This rulemaking does not... Georgia's ROP plan for the 1-hour ozone NAAQS for the Atlanta Area on April 26, 1999. See 64 FR 20196. \\3..., Paulding, and Rockdale. See 56 FR 56694, November 6, 1991. \\4\\ Seven additional ``ring'' counties...

  18. 78 FR 32135 - Approval and Promulgation of Implementation Plans; Atlanta, Georgia 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-05-29

    ... the 1-hour ozone NAAQS for the Atlanta Area on April 26, 1999. See 64 FR 20196. \\3\\ The 13-County... Area's original attainment date was June 15, 2007. See 69 FR 23951, April 30, 2004. The Atlanta Area.... See 73 FR 12013, March 6, 2008. When an area is reclassified, a new attainment date for...

  19. Trends analyses of 30 years of ambient 8 hour ozone and precursor monitoring data in the South Central U.S.: progress and challenges.

    PubMed

    Sather, Mark E; Cavender, Kevin

    2016-07-13

    In the last 30 years ambient ozone concentrations have notably decreased in the South Central U.S. Yet, current ambient ozone concentrations measured over the past three years 2013-2015 in this area of the U.S. are not meeting the U.S. 2015 8 hour ozone standard of 70 parts per billion (ppb). This paper provides an update on long-term trends analyses of ambient 8 hour ozone and ozone precursor monitoring data collected over the past 30 years (1986-2015) in four South Central U.S. cities, following up on two previously published reviews of 20 and 25 year trends for these cities. All four cities have benefitted from national ozone precursor controls put in place during the 1990s and 2000s involving cleaner vehicles (vehicle fleet turnover/replacement over time), cleaner fuels, cleaner gasoline and diesel engines, and improved inspection/maintenance programs for existing vehicles. Additional ozone precursor emission controls specific to each city are detailed in this paper. The controls have resulted in impressive ambient ozone and ambient ozone precursor concentration reductions in the four South Central U.S. cities over the past 30 years, including 31-70% ambient nitrogen oxides (NOx) concentration declines from historical peaks to the present, 43-72% volatile organic compound (VOC) concentration declines from historical peaks to the present, a related 45-76% VOC reactivity decline for a subset of VOC species from historical peaks to the present, and an 18-38 ppb reduction in city 8 hour ozone design value concentrations. A new challenge for each of the four South Central U.S. cities will be meeting the U.S. 2015 8 hour ozone standard of 70 ppb. PMID:27282109

  20. 75 FR 51960 - Proposed Rule To Implement the 1997 8-Hour Ozone National Ambient Air Quality Standard: New...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-24

    ... designation (for most areas the effective date of the 1997 8-hour designation was June 15, 2004). 40 CFR 51... (69 FR 23951, April 30, 2004). The rule further provides that an area remains subject to these applicable requirements until the area attains the 1997 8-hour NAAQS. 40 CFR 51.905(b). Additionally,...

  1. 75 FR 8331 - Adequacy Status of the Cincinnati, Ohio/Indiana Submitted 8-Hour Ozone Redesignation and...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-02-24

    ... submitted SIP budgets in our July 1, 2004, preamble starting at 69 FR 40038, and we used the information in... (NOx) as precursors to ozone in the Ohio and Indiana portions of the Cincinnati-Hamilton,...

  2. 76 FR 2829 - Approval and Promulgation of Air Quality Implementation Plans; Virginia; Adoption of 8-hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-18

    ... NAAQS for ozone on March 27, 2008 (73 FR 16436). II. Summary of SIP Revision On September 27, 2010, the... Budget under Executive Order 12866 (58 FR 51735, October 4, 1993); Does not impose an information...); Does not have Federalism implications as specified in Executive Order 13132 (64 FR 43255, August...

  3. 75 FR 47746 - Determination of Nonattainment and Reclassification of the Dallas/Fort Worth 1997 8-hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-09

    .... It is not usually emitted directly into the air, but at ground level is created by a chemical reaction between volatile organic compounds (VOCs) and oxides of nitrogen (NO X ) in the presence of... is more protective than the previous 1-hour ozone standard (62 FR 38855) that was established by...

  4. Eastern Texas Air Quality Forecasting System to Support TexAQS-II and 8-hour Ozone Modeling

    NASA Astrophysics Data System (ADS)

    Byun, D. W.

    2005-12-01

    The main objective of the Second Texas Air Quality Study (TexAQS-II) for 2005 and 2006 is to understand emissions and processes associated with the formation and transport of ozone and regional haze in Texas. The target research area is the more populated eastern half of the state, roughly from Interstate 35 eastward. Accurate meteorological and photochemical modeling efforts are essential to support this study and further enhance modeling efforts for establishing the State Implementation Plan (SIP) by Texas Commission on Environmental Quality (TCEQ). An air quality forecasting (AQF) system for Eastern Texas has been developed to provide these data and to further facilitate retrospective simulations to allow for model improvement and increased understanding of ozone episodes and emissions. We perform two-day air quality forecasting simulations with the 12-km Eastern Texas regional domain, and the 4-km Houston-Galveston area (HGA) domain utilizing a 48-CPU Beowulf Linux computer system. The dynamic boundary conditions are provided by the 36-km resolution conterminous US (CONUS) domain CMAQ simulations. Initial meteorological conditions are provided by the daily ETA forecast results. The results of individual runs are stored and made available to researchers and state and local officials via internet to study the patterns of air quality and its relationship to weather conditions and emissions. The data during the pre- and post-processing stages are in tens of gigabytes and must be managed efficiently during both the actual real-time and the subsequent computation periods. The nature of these forecasts and the time at which the initial data is available necessitates that models be executed within tight deadlines. A set of complex operational scripts is used to allow automatic operation of the data download, sequencing processors, performing graphical analysis, building database archives, and presenting on the web.

  5. 40 CFR Appendix I to Part 50 - Interpretation of the 8-Hour Primary and Secondary National Ambient Air Quality Standards for Ozone

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... and Secondary National Ambient Air Quality Standards for Ozone I Appendix I to Part 50 Protection of... Secondary National Ambient Air Quality Standards for Ozone 1. General. This appendix explains the data... secondary ambient air quality standards for ozone specified in § 50.10 are met at an ambient ozone...

  6. 40 CFR Appendix I to Part 50 - Interpretation of the 8-Hour Primary and Secondary National Ambient Air Quality Standards for Ozone

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... and Secondary National Ambient Air Quality Standards for Ozone I Appendix I to Part 50 Protection of... Secondary National Ambient Air Quality Standards for Ozone 1. General. This appendix explains the data... secondary ambient air quality standards for ozone specified in § 50.10 are met at an ambient ozone...

  7. 40 CFR Appendix I to Part 50 - Interpretation of the 8-Hour Primary and Secondary National Ambient Air Quality Standards for Ozone

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... and Secondary National Ambient Air Quality Standards for Ozone I Appendix I to Part 50 Protection of... Secondary National Ambient Air Quality Standards for Ozone 1. General. This appendix explains the data... secondary ambient air quality standards for ozone specified in § 50.10 are met at an ambient ozone...

  8. 40 CFR Appendix I to Part 50 - Interpretation of the 8-Hour Primary and Secondary National Ambient Air Quality Standards for Ozone

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... and Secondary National Ambient Air Quality Standards for Ozone I Appendix I to Part 50 Protection of... Secondary National Ambient Air Quality Standards for Ozone 1. General. This appendix explains the data... secondary ambient air quality standards for ozone specified in § 50.10 are met at an ambient ozone...

  9. A Procedure for Inter-Comparing the Skill of Regional-Scale Air Quality Model Simulations of Daily Maximum 8-Hour Ozone Concentrations

    EPA Science Inventory

    An operational model evaluation procedure is described to quantitatively assess the relative skill among several regionalscale air quality models simulating various percentiles of the cumulative frequency distribution of observed daily maximum 8-h ozone concentrations. Bootstrap ...

  10. 40 CFR 51.906 - Redesignation to nonattainment following initial designations for the 8-hour NAAQS.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... OF IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality... subsequently redesignated to nonattainment for the 8-hour ozone NAAQS, any absolute, fixed date applicable...

  11. 40 CFR 51.906 - Redesignation to nonattainment following initial designations for the 8-hour NAAQS.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... OF IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality... subsequently redesignated to nonattainment for the 8-hour ozone NAAQS, any absolute, fixed date applicable...

  12. 40 CFR 51.906 - Redesignation to nonattainment following initial designations for the 8-hour NAAQS.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... OF IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality... subsequently redesignated to nonattainment for the 8-hour ozone NAAQS, any absolute, fixed date applicable...

  13. 40 CFR 51.906 - Redesignation to nonattainment following initial designations for the 8-hour NAAQS.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... OF IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality... subsequently redesignated to nonattainment for the 8-hour ozone NAAQS, any absolute, fixed date applicable...

  14. 40 CFR Appendix I to Part 50 - Interpretation of the 8-Hour Primary and Secondary National Ambient Air Quality Standards for Ozone

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... decimal place of the computed value is rounded, with values equal to or greater than 5 rounding up. Thus....089 0.086 0.084 0.080 1995 98% 0.087 0.085 0.083 0.080 0.075 Average 98% (2) As shown in example...

  15. 40 CFR 51.915 - What emissions inventory requirements apply under the 8-hour NAAQS?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.915 What... emissions inventories for these areas, the ozone-relevant data element requirements under 40 CFR part...

  16. 40 CFR 51.915 - What emissions inventory requirements apply under the 8-hour NAAQS?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.915 What... emissions inventories for these areas, the ozone-relevant data element requirements under 40 CFR part...

  17. 40 CFR 51.915 - What emissions inventory requirements apply under the 8-hour NAAQS?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.915 What... emissions inventories for these areas, the ozone-relevant data element requirements under 40 CFR part...

  18. 40 CFR 51.913 - How do the section 182(f) NOX exemption provisions apply for the 8-hour NAAQS?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.913... designated nonattainment for the 8-hour ozone NAAQS and for any area in a section 184 ozone transport region...) A section 182(f) NOX exemption granted for the 1-hour ozone standard does not relieve the area...

  19. Average ozone vertical distribution at Sodankyla based on the 1988-1991 ozone sounding data

    NASA Technical Reports Server (NTRS)

    Kyro, Esko; Rummukainen, Markku; Taalas, Petteri; Supperi, Ari

    1994-01-01

    The study presents the statistical analysis of ozone sonde data obtained at Sodankyla (67.4 deg N, 26.6 deg E) from the beginning of the sounding program on March 1988 to the end of December 1991. The Sodankyla sounding data offers the longest continuous record of the ozone vertical distribution in the European Arctic. In this paper, we present the average ozone partial pressures within each 1 km column obtained for different seasons during the almost four year long period. We believe that the data represented here are useful as an interim reference ozone atmosphere, especially considering the fact that northern Scandinavia has become a popular campaign site for the big international ozone experiments.

  20. 77 FR 75386 - Approval and Promulgation of Air Quality Implementation Plans; Virginia; Fredericksburg 8-Hour...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-20

    ... From the Federal Register Online via the Government Publishing Office ENVIRONMENTAL PROTECTION...; Fredericksburg 8-Hour Ozone Maintenance Area Revision to Approved Motor Vehicle Emissions Budgets AGENCY: Environmental Protection Agency (EPA). ] ACTION: Final rule; correcting amendment. SUMMARY: This...

  1. 77 FR 65490 - Approval and Promulgation of Air Quality Implementation Plans; Virginia; Fredericksburg 8-Hour...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-10-29

    ... ambient air quality standard (NAAQS) for ozone. This action is being taken under the Clean Air Act (CAA... requirements of Section 12(d) of the National Technology Transfer and Advancement Act of 1995 (15 U.S.C. 272...; Fredericksburg 8-Hour Ozone Maintenance Area Revision to Approved Motor Vehicle Emissions Budgets...

  2. 40 CFR 51.915 - What emissions inventory requirements apply under the 8-hour NAAQS?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.915 What... emissions inventory requirement in section 172(c)(3) of the Act shall apply, and an emission inventory SIP... emissions inventories for these areas, the ozone-relevant data element requirements under 40 CFR part...

  3. 40 CFR 51.913 - How do the section 182(f) NOX exemption provisions apply for the 8-hour NAAQS?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... provisions apply for the 8-hour NAAQS? 51.913 Section 51.913 Protection of Environment ENVIRONMENTAL... IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.913... petition the Administrator for an exemption from NOX obligations under section 182(f) for any...

  4. 40 CFR 51.913 - How do the section 182(f) NOX exemption provisions apply for the 8-hour NAAQS?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... provisions apply for the 8-hour NAAQS? 51.913 Section 51.913 Protection of Environment ENVIRONMENTAL... IMPLEMENTATION PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.913... petition the Administrator for an exemption from NOX obligations under section 182(f) for any...

  5. 40 CFR 51.915 - What emissions inventory requirements apply under the 8-hour NAAQS?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... emissions inventories for these areas, the ozone-relevant data element requirements under 40 CFR part 51... nonattainment area subject only to title I, part D, subpart 1 of the Act in accordance with § 51.902(b), the... apply under the 8-hour NAAQS? 51.915 Section 51.915 Protection of Environment ENVIRONMENTAL...

  6. A Kalman-filter bias correction of ozone deterministic, ensemble-averaged, and probabilistic forecasts

    SciTech Connect

    Monache, L D; Grell, G A; McKeen, S; Wilczak, J; Pagowski, M O; Peckham, S; Stull, R; McHenry, J; McQueen, J

    2006-03-20

    Kalman filtering (KF) is used to postprocess numerical-model output to estimate systematic errors in surface ozone forecasts. It is implemented with a recursive algorithm that updates its estimate of future ozone-concentration bias by using past forecasts and observations. KF performance is tested for three types of ozone forecasts: deterministic, ensemble-averaged, and probabilistic forecasts. Eight photochemical models were run for 56 days during summer 2004 over northeastern USA and southern Canada as part of the International Consortium for Atmospheric Research on Transport and Transformation New England Air Quality (AQ) Study. The raw and KF-corrected predictions are compared with ozone measurements from the Aerometric Information Retrieval Now data set, which includes roughly 360 surface stations. The completeness of the data set allowed a thorough sensitivity test of key KF parameters. It is found that the KF improves forecasts of ozone-concentration magnitude and the ability to predict rare events, both for deterministic and ensemble-averaged forecasts. It also improves the ability to predict the daily maximum ozone concentration, and reduces the time lag between the forecast and observed maxima. For this case study, KF considerably improves the predictive skill of probabilistic forecasts of ozone concentration greater than thresholds of 10 to 50 ppbv, but it degrades it for thresholds of 70 to 90 ppbv. Moreover, KF considerably reduces probabilistic forecast bias. The significance of KF postprocessing and ensemble-averaging is that they are both effective for real-time AQ forecasting. KF reduces systematic errors, whereas ensemble-averaging reduces random errors. When combined they produce the best overall forecast.

  7. DEVELOMENT AND EVALUATION OF A MODEL FOR ESTIMATING LONG-TERM AVERAGE OZONE EXPOSURES TO CHILDREN

    EPA Science Inventory

    Long-term average exposures of school-age children can be modelled using longitudinal measurements collected during the Harvard Southern California Chronic Ozone Exposure Study over a 12-month period: June, 1995-May, 1996. The data base contains over 200 young children with perso...

  8. Radiative forcing and climate metrics for ozone precursor emissions: the impact of multi-model averaging

    NASA Astrophysics Data System (ADS)

    MacIntosh, C. R.; Shine, K. P.; Collins, W. J.

    2015-04-01

    Multi-model ensembles are frequently used to assess understanding of the response of ozone and methane lifetime to changes in emissions of ozone precursors such as NOx, VOCs (volatile organic compounds) and CO. When these ozone changes are used to calculate radiative forcing (RF) (and climate metrics such as the global warming potential (GWP) and global temperature-change potential (GTP)) there is a methodological choice, determined partly by the available computing resources, as to whether the mean ozone (and methane) concentration changes are input to the radiation code, or whether each model's ozone and methane changes are used as input, with the average RF computed from the individual model RFs. We use data from the Task Force on Hemispheric Transport of Air Pollution source-receptor global chemical transport model ensemble to assess the impact of this choice for emission changes in four regions (East Asia, Europe, North America and South Asia). We conclude that using the multi-model mean ozone and methane responses is accurate for calculating the mean RF, with differences up to 0.6% for CO, 0.7% for VOCs and 2% for NOx. Differences of up to 60% for NOx 7% for VOCs and 3% for CO are introduced into the 20 year GWP. The differences for the 20 year GTP are smaller than for the GWP for NOx, and similar for the other species. However, estimates of the standard deviation calculated from the ensemble-mean input fields (where the standard deviation at each point on the model grid is added to or subtracted from the mean field) are almost always substantially larger in RF, GWP and GTP metrics than the true standard deviation, and can be larger than the model range for short-lived ozone RF, and for the 20 and 100 year GWP and 100 year GTP. The order of averaging has most impact on the metrics for NOx, as the net values for these quantities is the residual of the sum of terms of opposing signs. For example, the standard deviation for the 20 year GWP is 2-3 times larger

  9. Radiative forcing and climate metrics for ozone precursor emissions: the impact of multi-model averaging

    NASA Astrophysics Data System (ADS)

    MacIntosh, C. R.; Shine, K. P.; Collins, W. J.

    2014-10-01

    Multi-model ensembles are frequently used to assess understanding of the response of ozone and methane lifetime to changes in emissions of ozone precursors such as NOx, VOC and CO. When these ozone changes are used to calculate radiative forcing (RF) (and climate metrics such as the global warming potential (GWP) and global temperature potential (GTP)) there is a methodological choice, determined partly by the available computing resources, as to whether the mean ozone (and methane lifetime) changes are input to the radiation code, or whether each model's ozone and methane changes are used as input, with the average RF computed from the individual model RFs. We use data from the Task Force on Hemispheric Transport of Air Pollution Source-Receptor global chemical transport model ensemble to assess the impact of this choice for emission changes in 4 regions (East Asia, Europe, North America and South Asia). We conclude that using the multi-model mean ozone and methane responses is accurate for calculating the mean RF, with differences up to 0.6% for CO, 0.7% for VOC and 2% for NOx. Differences of up to 60% for NOx 7% for VOC and 3% for CO are introduced into the 20 year GWP as a result of the exponential decay terms, with similar values for the 20 years GTP. However, estimates of the SD calculated from the ensemble-mean input fields (where the SD at each point on the model grid is added to or subtracted from the mean field) are almost always substantially larger in RF, GWP and GTP metrics than the true SD, and can be larger than the model range for short-lived ozone RF, and for the 20 and 100 year GWP and 100 year GTP. We find that the effect is generally most marked for the case of NOx emissions, where the net effect is a smaller residual of terms of opposing signs. For example, the SD for the 20 year GWP is two to three times larger using the ensemble-mean fields than using the individual models to calculate the RF. Hence, while the average of multi-model fields

  10. Exponential approximation for daily average solar heating or photolysis. [of stratospheric ozone layer

    NASA Technical Reports Server (NTRS)

    Cogley, A. C.; Borucki, W. J.

    1976-01-01

    When incorporating formulations of instantaneous solar heating or photolytic rates as functions of altitude and sun angle into long range forecasting models, it may be desirable to replace the time integrals by daily average rates that are simple functions of latitude and season. This replacement is accomplished by approximating the integral over the solar day by a pure exponential. This gives a daily average rate as a multiplication factor times the instantaneous rate evaluated at an appropriate sun angle. The accuracy of the exponential approximation is investigated by a sample calculation using an instantaneous ozone heating formulation available in the literature.

  11. Version 8 SBUV Ozone Profile Trends Compared with Trends from a Zonally Averaged Chemical Model

    NASA Technical Reports Server (NTRS)

    Rosenfield, Joan E.; Frith, Stacey; Stolarski, Richard

    2004-01-01

    Linear regression trends for the years 1979-2003 were computed using the new Version 8 merged Solar Backscatter Ultraviolet (SBUV) data set of ozone profiles. These trends were compared to trends computed using ozone profiles from the Goddard Space Flight Center (GSFC) zonally averaged coupled model. Observed and modeled annual trends between 50 N and 50 S were a maximum in the higher latitudes of the upper stratosphere, with southern hemisphere (SH) trends greater than northern hemisphere (NH) trends. The observed upper stratospheric maximum annual trend is -5.5 +/- 0.9 % per decade (1 sigma) at 47.5 S and -3.8 +/- 0.5 % per decade at 47.5 N, to be compared with the modeled trends of -4.5 +/- 0.3 % per decade in the SH and -4.0 +/- 0.2% per decade in the NH. Both observed and modeled trends are most negative in winter and least negative in summer, although the modeled seasonal difference is less than observed. Model trends are shown to be greatest in winter due to a repartitioning of chlorine species and the increasing abundance of chlorine with time. The model results show that trend differences can occur depending on whether ozone profiles are in mixing ratio or number density coordinates, and on whether they are recorded on pressure or altitude levels.

  12. 40 CFR 51.906 - Redesignation to nonattainment following initial designations for the 8-hour NAAQS.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... following initial designations for the 8-hour NAAQS. 51.906 Section 51.906 Protection of Environment... Standard § 51.906 Redesignation to nonattainment following initial designations for the 8-hour NAAQS. For any area that is initially designated attainment or unclassifiable for the 8-hour NAAQS and that...

  13. 40 CFR 51.907 - For an area that fails to attain the 8-hour NAAQS by its attainment date, how does EPA interpret...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.907 For an area that... 40 Protection of Environment 2 2012-07-01 2012-07-01 false For an area that fails to attain the 8... the CAA? 51.907 Section 51.907 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY...

  14. 40 CFR 51.907 - For an area that fails to attain the 8-hour NAAQS by its attainment date, how does EPA interpret...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.907 For an area that... 40 Protection of Environment 2 2014-07-01 2014-07-01 false For an area that fails to attain the 8... the CAA? 51.907 Section 51.907 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY...

  15. 75 FR 80340 - Approval and Promulgation of Implementation Plans; New Jersey; 8-Hour Ozone Control Measures

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-22

    ... consists of two new rules, Subchapter 26, ``Prevention of Air Pollution From Adhesives, Sealants, Adhesive Primers and Sealant Primers,'' and Subchapter 34, ``TBAC Emissions Reporting,'' (TBAC means tertiary butyl acetate or t-butyl acetate) and revisions to Subchapter 23, ``Prevention of Air Pollution...

  16. 75 FR 9781 - Determination of Nonattainment and Reclassification of the Atlanta, Georgia, 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-04

    ... standard, was approved by EPA on March 6, 2008 (73 FR 12013). However, EPA inadvertently excluded Hall... this action. Statutory and Executive Order Reviews Under Executive Order 12866 (58 FR 51735, October 4... Use'' (66 FR 28355, May 22, 2001). This action merely corrects an inadvertent error of omission in...

  17. 78 FR 45188 - Agency Information Collection Activities; Proposed Collection; Comment Request; 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-07-26

    ... Protection Agency, T.W. Alexander Drive, Research Triangle Park, NC 27711; telephone number: (919) 541-2363...., Monday through Friday, excluding legal holidays. The telephone number for the Reading Room is 202-566... information, including the validity of the methodology and assumptions used; (iii) enhance the...

  18. 78 FR 47572 - Disapproval of State Implementation Plan; Infrastructure Requirements for the 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-08-06

    ... restricted by statute. Certain other material, such as copyrighted material, is not placed on the Internet and will be publicly available only in hard copy form. Publicly available docket materials are..., section 110(a)(2)(E)(ii), is described in detail in our proposal of May 31, 2013 (78 FR 32613). The...

  19. 78 FR 32613 - Disapproval of State Implementation Plan; Infrastructure Requirements for the 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-05-31

    ... 0.12 parts per million (ppm) to 0.08 ppm (62 FR 38856). By statute, SIPs meeting the requirements of..., 2007, which was determined to be complete on March 27, 2008 (73 FR 16205), and another dated December 22, 2009. On May 19, 2011 (76 FR 28934), EPA published a notice of proposed rulemaking (NPR) for...

  20. 78 FR 32222 - Approval and Promulgation of Implementation Plans; Atlanta, Georgia 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-05-29

    ... 73 FR 16436. The current action, however, is being taken to address requirements under the earlier..., Gwinnett, Hall, Henry, Newton, Paulding, Rockdale, Spalding and Walton Counties in Georgia. EPA is...

  1. 78 FR 44439 - Approval and Promulgation of Implementation Plans: Atlanta, Georgia 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-07-24

    ... institute a second comment period on this action. DATES: The direct final rule published at 78 FR 32135 on... May 29, 2013 (78 FR 32135), EPA published a direct final rulemaking to approve Georgia's October 21... action, also published on May 29, 2013 (78 FR 32222). EPA will not institute a second comment period...

  2. 78 FR 34965 - Approval and Promulgation of Air Quality Implementation Plans; Ohio; 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-06-11

    ... accepted during the Regional Office ] normal hours of operation, and special arrangements should be made... second comment period. Any parties interested in commenting on this action should do so at this...

  3. 75 FR 42672 - Approval and Promulgation of Implementation Plans; New Jersey; 8-hour Ozone Control Measures

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-07-22

    ... conditionally approved. See 74 FR 22837 (May 15, 2009). If EPA approves this proposed SIP revision, the RACT... Subchapter 24 occurred on January 25, 2006 (71 FR 4045). EPA had previously approved Subchapter 24 provisions... FR 2938 (January 19, 2010). In this proposed rule, based upon reconsideration of the primary...

  4. 75 FR 26225 - Adequacy Status of the Chicago, Illinois Area Submitted 8-Hour Ozone Redesignation and...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-11

    ... budgets in our July 1, 2004, preamble starting at 69 FR 40038, and we used the information in these... Plans for Transportation Conformity Purposes AGENCY: Environmental Protection Agency (EPA). ACTION... conformity determinations. Illinois submitted a redesignation request and maintenance plan for the...

  5. 78 FR 34903 - Approval and Promulgation of Air Quality Implementation Plans; Ohio; 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-06-11

    ... section 176(c) of the CAA. See the official release of the MOVES2010 emissions model (75 FR 9411-9414) for... source emissions for criteria pollutants, including precursors. Transportation plans and projects... highway emissions. EPA announced the release of MOVES2010 on March 2, 2010 (75 FR 9411). Use of the...

  6. A New Method of Deriving Time-Averaged Tropospheric Column Ozone over the Tropics Using Total Ozone Mapping Spectrometer (TOMS) Radiances: Intercomparison and Analysis Using TRACE A Data

    NASA Technical Reports Server (NTRS)

    Kim, J. H.; Hudson, R. D.; Thompson, A. M.

    1996-01-01

    Error analysis of archived total 03 from total ozone mapping spectrometer (TOMS) (version 6) presented. Daily total 03 maps for the tropics, from the period October 6-21, 1992, are derived from TOMS radiances following correction for these errors. These daily maps, averaged together, show a wavelike feature, which is observed in all latitude bands, underlying sharp peaks which occur at different longitudes depending on the latitude. The wave pattern is used to derive both time-averaged stratospheric and tropospheric 03 fields. The nature of the wave pattern (stratospheric or tropospheric) cannot be determined with certainty due to missing data (no Pacific sondes, no lower stratospheric Stratospheric Aerosol and Gas Experiment (SAGE) ozone for 18 months after the Mt. Pinatubo eruption) and significant uncertainties in the corroborative satellite record in the lower stratosphere (solar backscattered ultraviolet (SBUV), microwave limb sounder (MLS)). However, the time- averaged tropospheric ozone field, based on the assumption that the wave feature is stratospheric, agrees within 10% with ultraviolet differential absorption laser Transport and Atmospheric Chemistry near the Equator-Atlantic) (TRACE A) 03 measurements from the DC-8 and with ozonesonde measurements over Brazzaville, Congo, Ascension Island, and Natal, Brazil, for the period October 6-21, 1992. The derived background (nonpolluted) Indian Ocean tropospheric ozone amount, 26 Dobson units (DU), agrees with the cleanest African ozonesonde profiles for September-October 1992. The assumption of a totally tropospheric wave (flat stratosphere) gives 38 DU above the western Indian Ocean and 15-40% disagreements with the sondes. Tropospheric column 03 is high from South America to Africa, owing to interaction of dynamics with biomass burning emissions. Comparison with fire distributions from advanced very high resolution radiometer (AVHHR) during October 1992 suggests that tropospheric 03 produced from biomass

  7. Ozone

    MedlinePlus

    ... reactive form of oxygen. In the upper atmosphere, ozone forms a protective layer that shields us from the sun’s ultraviolet rays. At ground level, ozone is a harmful air pollutant and a primary ...

  8. Ozone

    MedlinePlus

    Ozone is a gas. It can be good or bad, depending on where it is. "Good" ozone occurs naturally about 10 to 30 miles above ... the sun's ultraviolet rays. Part of the good ozone layer is gone. Man-made chemicals have destroyed ...

  9. A 4.8 hour periodicity in the spectra of Cyg X-3

    NASA Technical Reports Server (NTRS)

    Becker, R. H.; Robinson-Saba, J. L.; Boldt, E. A.; Holt, S. S.; Pravdo, S. H.; Serlemitsos, P. J.; Swank, J. H.

    1978-01-01

    The X-ray spectra from three observations of the X-ray binary Cyg X-3 by the cosmic X-ray spectroscopy experiment on OSO can be represented by power-law continua with strong iron line emission. Comparisons of spectra taken within the same observation at various phases of the 4.8 hour period reveal a relative excess of low energy X-ray emission near zero phase (i.e. the minimum) of the 4.8 hour modulation. In addition, the centroid of the line emission is observed to vary in phase with the 4.8 hour cycle. The possibility of persistent thermal X-ray emission from material surrounding the binary system is introduced in an effort to account for the observed effects.

  10. A survey of ozone concentrations in rural western Utah: unexpected results and spatial heterogeneity from 2010-2013

    NASA Astrophysics Data System (ADS)

    Arens, S. J.; Harper, K.

    2013-12-01

    Ozone concentrations and meteorological variables were monitored at eleven sites in rural western Utah during late spring through summer of 2010-2013 to determine regional background concentrations of ozone and to determine attainment or nonattainment of the ozone National Ambient Air Quality Standard (NAAQS). Ozone concentrations have been monitored along the Wasatch Front of Utah (Logan, Ogden, Salt Lake City and Provo) for 30 years by the Utah Division of Air Quality (DAQ), but no ozone data from outside the cities of Wasatch Front existed prior to 2010. All rural sites, except Badger Springs, west of St. George, UT, were in attainment of the ozone NAAQS, which is 75 ppb averaged over 8 hours. However, ozone concentrations were higher than expected at seven of the eleven sites. All eleven sites were located in either small rural towns or uninhabited areas of western Utah, which were distant from anthropogenic emissions of ozone precursors. In 2010, ozone concentrations were relatively low along the Wasatch Front of Utah. Ozone concentrations exceeded 65 ppb for one day at three of four rural sites. Ozone concentrations at two of the four sites were generally in the range of expected rural ozone concentrations of 50-60 ppb. Ozone concentrations during 2011-2012 were higher throughout Utah compared to 2010. In 2011, 8-hour ozone concentrations exceeded 70 ppb for at least one day at four of five sites. The maximum 8-hour ozone concentration was 78 ppb, observed at Lytle Ranch, west of St. George, UT. Ozone concentrations at only one rural Utah site were in the expected range of 50-60 ppb. Ozone concentrations during 2012 were the highest observed during the four years of the study with 8-hour ozone concentrations exceeding 75 ppb at three of five rural sites and exceeding 70 ppb for at least four days at four of five sites. Although data collected was not considered regulatory by the EPA, the ozone NAAQS was exceeded at Badger Springs in southwestern Utah. Ozone

  11. New ozone standard in the U.S.A. applied to Mexico City metropolitan air quality

    SciTech Connect

    Bravo A, H. Sosa E, R.; Sanchez A, P.; Jaimes P, M.

    1998-12-31

    The air quality of the Mexico City Metropolitan Zone (MCMZ) is recognized as one of the worst air pollution problems in the world. At the present, ozone is the most critical atmospheric pollutant in the area. According to the air quality data of the monitoring station at the University of Mexico, the ozone problem started in 1986. Mexican Ozone Air Quality Standard (MOAQS) specifies that a concentration of 0.11 ppm must not be exceeded more than one hour a day, one day a year in the term of three years. The Official Air Quality Data (RAMA) from 19 monitoring stations in the MCMZ coincides with the University station`s data, presenting the same atmospheric pollution problem. In the most critical sites the MOAQS is exceeded more than 1,300 hours in a year. Now, the Environmental Protection Agency of the United States (EPA) is working to establish the new ozone standard. EPA is setting the standard at 0.08 ppm on an average of 8 hours, considering the 3 year average of the annual 4th highest daily maximum 8 hour ozone concentration. The purpose of this paper is to present the tendency and comparison between two standards (1 hour and 8 hours) of the ozone concentrations in the MCMZ, since 1986 to 1996. Although Mexico does not yet have the 8 hour standard for ozone, it is very important to analyze the existing air quality data with this new standard. In this way the aim is to protect the health of more than 20 million inhabitants in the MCMZ.

  12. Ozone

    SciTech Connect

    Not Available

    1988-06-01

    The author discusses the debate over whether concern about a hole in the ozone layer in Antarctic is real or science fiction. There is a growing consensus that efforts must be taken to protect the ozone layer. The issue now is not whether chlorofluorocarbons (CFCs) should be controlled and regulated but how much and how soon. The United States has urged that the production of dangerous CFCs, and any other chemicals that affect the ozone layer, be restricted immediately to current levels and that their use be reduced 95 percent over the next decade. The American position was too strong for many European nations and the Japanese. Negotiations at an international conference on the matter broke down. The breakdown is due in part to a more acute concern for environmental matters in the United States than exists in many countries. Meanwhile CFCs are linked to another environmental problem that equally threatens the world - the Greenhouse Effect. The earth is in a natural warming period, but man could be causing it to become even warmer. The Greenhouse Effect could have a catastrophic impact on mankind, although nothing has been proven yet.

  13. 75 FR 80420 - Reasonable Further Progress Requirements for the 1997 8-Hour Ozone National Ambient Air Quality...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-22

    ... discussion of EPA's rationale for applying this interpretation in the Phase 2 Rule, see 70 FR at 71647- 49... FR 71612, November 29, 2005). \\2\\ The memorandum is available on the EPA Technology and Transfer... approach for crediting reductions from outside nonattainment areas (``outside'' reductions). See 72...

  14. 77 FR 35285 - Approval of Air Quality Implementation Plan; Arizona; Attainment Plan for 1997 8-Hour Ozone Standard

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-06-13

    ... Order Reviews I. Proposed Action On April 11, 2012 (70 FR 21690), EPA proposed to approve the ``Eight... Budget under Executive Order 12866 (58 FR 51735, October 4, 1993); Does not impose an information...); Does not have Federalism implications as specified in Executive Order 13132 (64 FR 43255, August...

  15. 76 FR 3840 - Approval of One-Year Extension for Attaining the 1997 8-Hour Ozone Standard for the Delaware...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-21

    ... November 9, 2010 (75 FR 68736), EPA published a notice of proposed rulemaking (NPR) for the States. The NPR... Executive Order Reviews A. General Requirements Under Executive Order 12866 (58 FR 51735, October 4, 1993...'' (66 FR 28355, May 22, 2001). This action merely approves state law as meeting Federal requirements...

  16. 76 FR 3838 - Approval and Promulgation of One-Year Extension for Attaining the 1997 8-Hour Ozone Standard for...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-21

    ... attainment date be extended to June 15, 2011. On November 9, 2010 (75 FR 68733), EPA proposed to approve New...).'' IV. Statutory and Executive Order Reviews Under Executive Order 12866 (58 FR 51735, October 4, 1993...'' (66 FR 28355 (May 22, 2001)). This action merely finds that an area has qualified for a...

  17. 75 FR 68736 - Approval of One-Year Extension for Attaining the 1997 8-Hour Ozone Standard for the Delaware...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-11-09

    ...'' subject to review by the Office of Management and Budget under Executive Order 12866 (58 FR 51735, October... Executive Order 13132 (64 FR 43255, August 10, 1999); Is not an economically significant regulatory action based on health or safety risks subject to Executive Order 13045 (62 FR 19885, April 23, 1997); ] Is...

  18. 75 FR 43069 - Approval of One-Year Extension for Attaining the 1997 8-Hour Ozone Standard in the Baltimore...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-07-23

    ... Concerning Regulations That Significantly Affect Energy Supply, Distribution, or Use'' (66 FR 28355 (May 22... From the Federal Register Online via the Government Publishing Office ENVIRONMENTAL PROTECTION... Baltimore Moderate Nonattainment Area AGENCY: Environmental Protection Agency (EPA). ACTION: Direct...

  19. 78 FR 34906 - Approval and Promulgation of Air Quality Implementation Plans; Ohio; Lima 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-06-11

    ... the following methods: 1. www.regulations.gov : Follow the on-line instructions for submitting....regulations.gov , including any personal information provided, unless the comment includes information claimed....regulations.gov or email. The www.regulations.gov Web site is an ``anonymous access'' system, which means...

  20. 75 FR 43114 - Approval of One-Year Extension for Attaining the 1997 8-Hour Ozone Standard in the Baltimore...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-07-23

    ... the following methods: A. http://www.regulations.gov . Follow the on-line instructions for submitting... the use of special characters, any form of encryption, and be free of any defects or viruses....

  1. 75 FR 16456 - Adequacy Status of the Beaumont-Port Arthur, TX Maintenance Plan; 8-Hour Ozone Motor Vehicle...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-04-01

    ...; Transportation Conformity Rule Amendments: Response to Court Decision and Additional Rule Changes'' (69 FR 40004... been made, pursuant to 40 CFR 93.104(e). See, 73 FR 4419 (January 24, 2008). Authority: 42 U.S.C. 7401... motor vehicle emissions budgets (MVEB) in the Beaumont-Port Arthur, Texas (BPA) Redesignation...

  2. 78 FR 34965 - Approval and Promulgation of Air Quality Implementation Plans; Ohio; Lima 1997 8-Hour Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-06-11

    ... arrangements should be made for deliveries of boxed information. The Regional Office official hours of business... second comment period. Any parties interested in commenting on this action should do so at this...

  3. 75 FR 55977 - Adequacy Status of the Knoxville, TN 1997 8-Hour Ozone Maintenance Plan Motor Vehicle Emission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-15

    ... Additional Rule Changes'' (69 FR 40004). Please note that an adequacy review is separate from EPA's... made, pursuant to 40 CFR 93.104(e). See 73 FR 4419 (January 24, 2008). Authority: 42 U.S.C. 7401 et seq... Vehicle Emission Budgets for Transportation Conformity Purposes AGENCY: Environmental Protection...

  4. 76 FR 28223 - Adequacy Status of the Baton Rouge, Louisiana Maintenance Plan 8-Hour Ozone Motor Vehicle...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-16

    ... Additional Rule Changes'' (69 FR 40004). Please note that an adequacy review is separate from EPA's... the new MVEB if the demonstration has not already been made, pursuant to 40 CFR 93.104(e). See, 73 FR... Emission Budgets for Transportation Conformity Purposes AGENCY: Environmental Protection Agency...

  5. 78 FR 7429 - Adequacy Status of the Dallas-Fort Worth, TX Reasonable Further Progress 8-Hour Ozone Motor...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-01

    ...: Response to Court Decision and Additional Rule Changes'' (69 FR 40004). Please note that an adequacy review..., pursuant to 40 CFR 93.104(e). See, 73 FR 4419 (January 24, 2008). Authority: 42 U.S.C. 7401 et seq. Dated... Vehicle Emission Budgets for Transportation Conformity Purposes AGENCY: Environmental Protection...

  6. 75 FR 9893 - Adequacy Determination for the Denver Metro Area and North Front Range 8-Hour Ozone Attainment...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-04

    ... North Front Range Metropolitan Planning Organization (NFR MPO), the Colorado Department of...) which was promulgated August 15, 1997 (see 62 FR 43780). We described our process for determining the adequacy of submitted SIP MVEBs in our July 1, 2004 Transportation Conformity Rule Amendments (see 69...

  7. 77 FR 21690 - Approval and Promulgation of Air Quality Implementation Plan for 1997 8-Hour Ozone Standard; Arizona

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-04-11

    .../Projects/Project.asp?CMSID2=1120 &MID=Environmental%20Programs. In June 2007, the United States Court of... documentation in their submittals explaining how the emissions data were calculated. See 70 FR 71612 (Nov. 29... is proposing to approve revisions to the Arizona state implementation plan (SIP) that...

  8. 40 CFR 52.1342 - Control strategy: Ozone.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-IL) metropolitan 1997 8-hour ozone nonattainment area has attained the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR 51.918, suspends the requirements for this area to submit an attainment... measures, and other plan elements related to attainment of the standards for as long as the area...

  9. 77 FR 73570 - Approval and Promulgation of Implementation Plans; New Jersey and New York Ozone Attainment...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-11

    ... 8-hour ozone implementation rule, published on November 29, 2005 (70 FR 71612) (Phase 2 Rule... of the 2008 ozone NAAQS. \\2\\ See 73 FR 16436; March 27, 2008. For a detailed explanation of the... to address the requirements of the 1997 8-hour ozone standard: On July 17, 2008 (73 FR 41068),...

  10. 40 CFR 51.913 - How do the section 182(f) NOX exemption provisions apply for the 8-hour NAAQS?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 2 2011-07-01 2011-07-01 false How do the section 182(f) NOX exemption... How do the section 182(f) NOX exemption provisions apply for the 8-hour NAAQS? (a) A person may petition the Administrator for an exemption from NOX obligations under section 182(f) for any...

  11. 40 CFR 51.913 - How do the section 182(f) NOX exemption provisions apply for the 8-hour NAAQS?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 2 2013-07-01 2013-07-01 false How do the section 182(f) NOX exemption... How do the section 182(f) NOX exemption provisions apply for the 8-hour NAAQS? (a) A person may petition the Administrator for an exemption from NOX obligations under section 182(f) for any...

  12. Synoptic and meteorological drivers of extreme ozone concentrations over Europe

    NASA Astrophysics Data System (ADS)

    Otero, Noelia Felipe; Sillmann, Jana; Schnell, Jordan L.; Rust, Henning W.; Butler, Tim

    2016-04-01

    The present work assesses the relationship between local and synoptic meteorological conditions and surface ozone concentration over Europe in spring and summer months, during the period 1998-2012 using a new interpolated data set of observed surface ozone concentrations over the European domain. Along with local meteorological conditions, the influence of large-scale atmospheric circulation on surface ozone is addressed through a set of airflow indices computed with a novel implementation of a grid-by-grid weather type classification across Europe. Drivers of surface ozone over the full distribution of maximum daily 8-hour average values are investigated, along with drivers of the extreme high percentiles and exceedances or air quality guideline thresholds. Three different regression techniques are applied: multiple linear regression to assess the drivers of maximum daily ozone, logistic regression to assess the probability of threshold exceedances and quantile regression to estimate the meteorological influence on extreme values, as represented by the 95th percentile. The relative importance of the input parameters (predictors) is assessed by a backward stepwise regression procedure that allows the identification of the most important predictors in each model. Spatial patterns of model performance exhibit distinct variations between regions. The inclusion of the ozone persistence is particularly relevant over Southern Europe. In general, the best model performance is found over Central Europe, where the maximum temperature plays an important role as a driver of maximum daily ozone as well as its extreme values, especially during warmer months.

  13. Observation of gamma rays with a 4.8 hour periodicity from CYG X-3

    NASA Technical Reports Server (NTRS)

    Lamb, R. C.; Fichtel, C. E.; Hartman, R. C.; Kniffen, D. A.; Thompson, D. J.

    1976-01-01

    Energetic (E35 MeV) Gamma rays were observed from Cyg X-3 with the SAS-2 Gamma ray telescope. They are modulated at the 4.8 sup h period observed in the X-ray and infrared regions, and within the statistical error are in phase with this emission. The flux above 100 MeV has an average value of (4.4 + or - 1.1)x 10 to the -6 power/sq cm/sec. If the distance to Cyg X-3 is 10 kpcs, this flux implies a luminosity of more than 10 to the 37th power ergs/s if the radiation is isotropic and about 10 to the 36th power ergs/s if the radiation is restricted to a cone of one steradian, as it might be in a pulsar.

  14. Behavioral changes in neonatal swine after an 8-hour rest during prolonged transportation.

    PubMed

    Williams, J L; Richert, B T; Marchant-Forde, J N; Eicher, S D

    2012-09-01

    Long distance transportation of weaned piglets (Sus scrofa) is increasingly common in the united states and may result in delayed eating, drinking, or normal social behaviors. A potential solution is a mid-journey rest (lairage). The objective of this study was to determine if a lairage altered behavior after a 16-h transport. Pigs that weighed approximately 18 kg each (n = 894) were housed in 16 pens with 8 pens per treatment. Lairaged pigs were transported for 8 h and given an 8-h rest with food and water, whereas control pigs were transported continuously for 16 h. The heaviest, the lightest, and 2 average-BW pigs relative to the average weight of the pen were observed by video recording for 24 h immediately before and after transport, and during d 6 and 13 after transport. Postures (lying, sitting, and standing) were recorded using 10-min-interval scan sampling, and behavioral categories included inactivity, activities (eating, drinking, alert, manipulating pen, rooting, and walking) and social interactions (aggression, belly nosing, playing, tail biting, and positive social behaviors). In both treatments, sitting occurred most before transport (P < 0.01) than at other times, but did not differ between treatments. Standing increased (time effect; P < 0.01) for both treatments immediately after transport through d 6, but returned to pre-transport values by d 13. In contrast, lying decreased (time effect; P < 0.01) after transport, but returned to above pre-transport values by d 13. Time effects were evident for activity (P < 0.01), pen manipulation (P = 0.05), rooting (P < 0.01), initiation of belly-nosing (P = 0.01), and receiving belly-nosing (P = 0.03); however, initiation of aggression did not differ for day (P = 0.19) or treatment (P = 0.56). Lairaged pigs initiated more (P = 0.05) play than continuously transported pigs, but no differences (P = 0.84) were seen in receipt of play behavior. Pigs that were to be transported for 16 h continuously walked less

  15. 40 CFR 52.2125 - Control strategy: Ozone.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR 51.918, suspends the... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.2125... strategy: Ozone. (a) Determination of attaining data. EPA has determined, as of November 15, 2011, the...

  16. 40 CFR 52.1779 - Control strategy: Ozone.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR 51.918, suspends the... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.1779... strategy: Ozone. (a) Determination of attaining data. EPA has determined, as of November 15, 2011, the...

  17. 40 CFR 52.2125 - Control strategy: Ozone.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR 51.918, suspends the... 40 Protection of Environment 5 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.2125... strategy: Ozone. (a) Determination of attaining data. EPA has determined, as of November 15, 2011, the...

  18. 40 CFR 52.1779 - Control strategy: Ozone.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR 51.918, suspends the... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.1779... strategy: Ozone. (a) Determination of attaining data. EPA has determined, as of November 15, 2011, the...

  19. 40 CFR 52.2125 - Control strategy: Ozone.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR 51.918, suspends the... 40 Protection of Environment 5 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.2125... strategy: Ozone. (a) Determination of attaining data. EPA has determined, as of November 15, 2011, the...

  20. Impact of climate change on ambient ozone level and mortality in southeastern United States.

    PubMed

    Chang, Howard H; Zhou, Jingwen; Fuentes, Montserrat

    2010-07-01

    There is a growing interest in quantifying the health impacts of climate change. This paper examines the risks of future ozone levels on non-accidental mortality across 19 urban communities in Southeastern United States. We present a modeling framework that integrates data from climate model outputs, historical meteorology and ozone observations, and a health surveillance database. We first modeled present-day relationships between observed maximum daily 8-hour average ozone concentrations and meteorology measured during the year 2000. Future ozone concentrations for the period 2041 to 2050 were then projected using calibrated climate model output data from the North American Regional Climate Change Assessment Program. Daily community-level mortality counts for the period 1987 to 2000 were obtained from the National Mortality, Morbidity and Air Pollution Study. Controlling for temperature, dew-point temperature, and seasonality, relative risks associated with short-term exposure to ambient ozone during the summer months were estimated using a multi-site time series design. We estimated an increase of 0.43 ppb (95% PI: 0.14-0.75) in average ozone concentration during the 2040's compared to 2000 due to climate change alone. This corresponds to a 0.01% increase in mortality rate and 45.2 (95% PI: 3.26-87.1) premature deaths in the study communities attributable to the increase in future ozone level.

  1. Cerebral blood flow determination within the first 8 hours of cerebral infarction using stable xenon-enhanced computed tomography

    SciTech Connect

    Hughes, R.L.; Yonas, H.; Gur, D.; Latchaw, R.

    1989-06-01

    Cerebral blood flow mapping with stable xenon-enhanced computed tomography (Xe/CT) was performed in conjunction with conventional computed tomography (CT) within the first 8 hours after the onset of symptoms in seven patients with cerebral infarction. Six patients had hemispheric infarctions, and one had a progressive brainstem infarction. Three patients with very low (less than 10 ml/100 g/min) blood flow in an anatomic area appropriate for the neurologic deficit had no clinical improvement by the time of discharge from the hospital; follow-up CT scans of these three patients confirmed infarction in the area of very low blood flow. Three patients with moderate blood flow reductions (15-45 ml/100 g/min) in the appropriate anatomic area had significant clinical improvement from their initial deficits and had normal follow-up CT scans. One patient studied 8 hours after stroke had increased blood flow (hyperemia) in the appropriate anatomic area and made no clinical recovery.

  2. Unraveling the sources of ground level ozone in the Intermountain Western United States using Pb isotopes.

    PubMed

    Christensen, John N; Weiss-Penzias, Peter; Fine, Rebekka; McDade, Charles E; Trzepla, Krystyna; Brown, Shaun T; Gustin, Mae Sexauer

    2015-10-15

    Ozone as an atmospheric pollutant is largely produced by anthropogenic precursors and can significantly impact human and ecosystem health, and climate. The U.S. Environmental Protection Agency has recently proposed lowering the ozone standard from 75 ppbv (MDA8 = Maximum Daily 8-Hour Average) to between 65 and 70 ppbv. This will result in remote areas of the Intermountain West that includes many U.S. National Parks being out of compliance, despite a lack of significant local sources. We used Pb isotope fingerprinting and back-trajectory analysis to distinguish sources of imported ozone to Great Basin National Park in eastern Nevada. During discrete Chinese Pb events (> 1.1 ng/m(3) & > 80% Asian Pb) trans-Pacific transported ozone was 5 ± 5.5 ppbv above 19 year averages for those dates. In contrast, concentrations during regional transport from the Los Angeles and Las Vegas areas were 15 ± 2 ppbv above the long-term averages, and those characterized by high-altitude transport 3 days prior to sampling were 19 ± 4ppbv above. However, over the study period the contribution of trans-Pacific transported ozone increased at a rate of 0.8 ± 0.3 ppbv/year, suggesting that Asian inputs will exceed regional and high altitude sources by 2015-2020. All of these sources will impact regulatory compliance with a new ozone standard, given increasing global background.

  3. Unraveling the sources of ground level ozone in the Intermountain Western United States using Pb isotopes.

    PubMed

    Christensen, John N; Weiss-Penzias, Peter; Fine, Rebekka; McDade, Charles E; Trzepla, Krystyna; Brown, Shaun T; Gustin, Mae Sexauer

    2015-10-15

    Ozone as an atmospheric pollutant is largely produced by anthropogenic precursors and can significantly impact human and ecosystem health, and climate. The U.S. Environmental Protection Agency has recently proposed lowering the ozone standard from 75 ppbv (MDA8 = Maximum Daily 8-Hour Average) to between 65 and 70 ppbv. This will result in remote areas of the Intermountain West that includes many U.S. National Parks being out of compliance, despite a lack of significant local sources. We used Pb isotope fingerprinting and back-trajectory analysis to distinguish sources of imported ozone to Great Basin National Park in eastern Nevada. During discrete Chinese Pb events (> 1.1 ng/m(3) & > 80% Asian Pb) trans-Pacific transported ozone was 5 ± 5.5 ppbv above 19 year averages for those dates. In contrast, concentrations during regional transport from the Los Angeles and Las Vegas areas were 15 ± 2 ppbv above the long-term averages, and those characterized by high-altitude transport 3 days prior to sampling were 19 ± 4ppbv above. However, over the study period the contribution of trans-Pacific transported ozone increased at a rate of 0.8 ± 0.3 ppbv/year, suggesting that Asian inputs will exceed regional and high altitude sources by 2015-2020. All of these sources will impact regulatory compliance with a new ozone standard, given increasing global background. PMID:25934382

  4. Ozone Air Quality Impacts of Shale Gas Development in South Texas Urban Areas

    NASA Astrophysics Data System (ADS)

    Chang, C.; Liao, K.

    2013-12-01

    Recent technological advances, mainly horizontal drilling and hydraulic fracturing, and continued drilling in shale, have increased domestic production of oil and gas in the United State (U.S.). However, shale gas developments could also affect the environment and human health, particularly in areas where oil and gas developments are new activities. This study is focused on the impacts of shale gas developing activities on summertime ozone air quality in South Texas urban areas since many of them are already ozone nonattainment areas. We use an integrated approach to investigate the ozone air quality impact of the shale gas development in South Texas urban areas. They are: (1) satellite measurement of precursors, (2) observations of ground-level ozone concentrations, and (3) air mass trajectory modeling. Nitrogen dioxide (NO2) is an important precursor to ozone formation, and summertime average tropospheric nitrogen dioxide (NO2) column densities measured by the National Aeronautics and Space Administration's Ozone Monitoring Instrument increased in the South Texas shale area (i.e., the Eagle Ford Shale area) in 2011 and 2012 as compared to 2008-2010. The U.S. Environmental Protection Agency's ground-level observations showed summertime average and peak ozone (i.e., the 4th highest daily maximum 8-hour average ozone) concentrations slightly increased from 2010 to 2012 in Austin and San Antonio. However, the frequencies of peak ozone concentrations above the 75ppb ozone standard have been significantly increasing since 2011 in Austin and San Antonio. It is expected to increase the possibilities of violating the ozone National Ambient Air Quality Standard (NAAQS) for South Texas urban areas in the future. The results of trajectory modeling showed air masses transported from the southeastern Texas could reach Austin and San Antonio and confirmed that emissions from the Eagle Ford Shale area could affect ozone air quality in South Texas urban areas in 2011 and 2012

  5. Gridded global surface ozone metrics for atmospheric chemistry model evaluation

    NASA Astrophysics Data System (ADS)

    Sofen, E. D.; Bowdalo, D.; Evans, M. J.; Apadula, F.; Bonasoni, P.; Cupeiro, M.; Ellul, R.; Galbally, I. E.; Girgzdiene, R.; Luppo, S.; Mimouni, M.; Nahas, A. C.; Saliba, M.; Tørseth, K.

    2016-02-01

    The concentration of ozone at the Earth's surface is measured at many locations across the globe for the purposes of air quality monitoring and atmospheric chemistry research. We have brought together all publicly available surface ozone observations from online databases from the modern era to build a consistent data set for the evaluation of chemical transport and chemistry-climate (Earth System) models for projects such as the Chemistry-Climate Model Initiative and Aer-Chem-MIP. From a total data set of approximately 6600 sites and 500 million hourly observations from 1971-2015, approximately 2200 sites and 200 million hourly observations pass screening as high-quality sites in regionally representative locations that are appropriate for use in global model evaluation. There is generally good data volume since the start of air quality monitoring networks in 1990 through 2013. Ozone observations are biased heavily toward North America and Europe with sparse coverage over the rest of the globe. This data set is made available for the purposes of model evaluation as a set of gridded metrics intended to describe the distribution of ozone concentrations on monthly and annual timescales. Metrics include the moments of the distribution, percentiles, maximum daily 8-hour average (MDA8), sum of means over 35 ppb (daily maximum 8-h; SOMO35), accumulated ozone exposure above a threshold of 40 ppbv (AOT40), and metrics related to air quality regulatory thresholds. Gridded data sets are stored as netCDF-4 files and are available to download from the British Atmospheric Data Centre (doi: 10.5285/08fbe63d-fa6d-4a7a-b952-5932e3ab0452). We provide recommendations to the ozone measurement community regarding improving metadata reporting to simplify ongoing and future efforts in working with ozone data from disparate networks in a consistent manner.

  6. Antarctic Ozone Hole, 2000

    NASA Technical Reports Server (NTRS)

    2002-01-01

    Each spring the ozone layer over Antarctica nearly disappears, forming a 'hole' over the entire continent. The hole is created by the interaction of some man-made chemicals-freon, for example-with Antarctica's unique weather patterns and extremely cold temperatures. Ozone in the stratosphere absorbs ultraviolet radiation from the sun, thereby protecting living things. Since the ozone hole was discovered many of the chemicals that destroy ozone have been banned, but they will remain in the atmosphere for decades. In 2000, the ozone hole grew quicker than usual and exceptionally large. By the first week in September the hole was the largest ever-11.4 million square miles. The top image shows the average total column ozone values over Antarctica for September 2000. (Total column ozone is the amount of ozone from the ground to the top of the atmosphere. A relatively typical measurement of 300 Dobson Units is equivalent to a layer of ozone 0.12 inches thick on the Earth's surface. Levels below 220 Dobson Units are considered to be significant ozone depletion.) The record-breaking hole is likely the result of lower than average ozone levels during the Antarctic fall and winter, and exceptionally cold temperatures. In October, however (bottom image), the hole shrank dramatically, much more quickly than usual. By the end of October, the hole was only one-third of it's previous size. In a typical year, the ozone hole does not collapse until the end of November. NASA scientists were surprised by this early shrinking and speculate it is related to the region's weather. Global ozone levels are measured by the Total Ozone Mapping Spectrometer (TOMS). For more information about ozone, read the Earth Observatory's ozone fact sheet, view global ozone data and see these ozone images. Images by Greg Shirah, NASA GSFC Scientific Visualization Studio.

  7. 40 CFR 52.582 - Control strategy: Ozone.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... area has attaining data for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR... satisfies 40 CFR 58.20(f) which requires the State to provide for the establishment and maintenance of... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.582...

  8. 40 CFR 52.582 - Control strategy: Ozone.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... data for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR 51.918, suspends..., into the Georgia State Implementation Plan. This submittal satisfies 40 CFR 58.20(f) which requires the... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.582...

  9. 40 CFR 52.582 - Control strategy: Ozone.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... area has attaining data for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR... satisfies 40 CFR 58.20(f) which requires the State to provide for the establishment and maintenance of... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.582...

  10. Alternative ozone metrics and daily mortality in Suzhou: the China Air Pollution and Health Effects Study (CAPES).

    PubMed

    Yang, Chunxue; Yang, Haibing; Guo, Shu; Wang, Zongshuang; Xu, Xiaohui; Duan, Xiaoli; Kan, Haidong

    2012-06-01

    Controversy remains regarding the relationship between various metrics of ozone (O(3)) and mortality. In China, the largest developing country, there have been few studies investigating the acute effect of O(3) on death. We used three exposure metrics of O(3) (1-hour maximum, maximum 8-hour average and 24-hour average) to examine its short-term association with daily mortality in Suzhou, China. We used a Generalized Additive Model (GAM) with penalized splines to analyze the mortality, O(3), and covariate data. We examined the association by season, age group, sex and educational level. We found that the current level of O(3) in Suzhou is associated with death rates from all causes and cardiovascular diseases. Among various metrics of O(3), maximum 8-hour average and 1-hour maximum concentrations seem to be more strongly associated with increased mortality rate compared to 24-hour average concentrations. Using maximum 8-hour average, an inter-quartile range increase of 2-day average O(3) (lag 01) corresponds to 2.15% (95%CI, 0.36 to 3.93), 4.47% (95%CI, 1.43 to 7.51), -1.85% (95%CI, -6.91 to 3.22) increase in all-cause, cardiovascular, and respiratory mortality, respectively. The associations between O(3) and daily mortality appeared to be more evident in the cool season than in the warm season. In conclusion, maximum 8-hour average and 1-hour maximum concentrations of O(3) are associated with daily mortality in Suzhou. Our analyses strengthen the rationale for further limiting levels of O(3) pollution in the city. PMID:22521098

  11. 75 FR 2935 - Extension of Deadline for Promulgating Designations for the 2008 Ozone National Ambient Air...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-01-19

    ..., 2008, EPA promulgated revised 8-hour primary and secondary ozone NAAQS (73 FR 16436; March 27, 2008... Protection Agency 40 CFR Parts 50, 58 and 81 Ozone National Ambient Air Quality Standards; Final Rule and... Designations for the 2008 Ozone National Ambient Air Quality Standards AGENCY: Environmental Protection...

  12. 40 CFR 50.15 - National primary and secondary ambient air quality standards for ozone.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... air quality standards for ozone. 50.15 Section 50.15 Protection of Environment ENVIRONMENTAL....15 National primary and secondary ambient air quality standards for ozone. (a) The level of the national 8-hour primary and secondary ambient air quality standards for ozone (O3) is 0.075 parts...

  13. 40 CFR 50.15 - National primary and secondary ambient air quality standards for ozone.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... air quality standards for ozone. 50.15 Section 50.15 Protection of Environment ENVIRONMENTAL....15 National primary and secondary ambient air quality standards for ozone. (a) The level of the national 8-hour primary and secondary ambient air quality standards for ozone (O3) is 0.075 parts...

  14. 40 CFR 52.2043 - Control strategy for maintenance plans: ozone.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...: ozone. 52.2043 Section 52.2043 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control strategy for maintenance plans: ozone. (a) As of December 26, 2013, EPA approves the following... (VOCs) for the Lancaster 1997 8-Hour Ozone Maintenance Area submitted by the Secretary of...

  15. 40 CFR 50.15 - National primary and secondary ambient air quality standards for ozone.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... air quality standards for ozone. 50.15 Section 50.15 Protection of Environment ENVIRONMENTAL....15 National primary and secondary ambient air quality standards for ozone. (a) The level of the national 8-hour primary and secondary ambient air quality standards for ozone (O3) is 0.075 parts...

  16. 40 CFR 50.15 - National primary and secondary ambient air quality standards for ozone.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... air quality standards for ozone. 50.15 Section 50.15 Protection of Environment ENVIRONMENTAL....15 National primary and secondary ambient air quality standards for ozone. (a) The level of the national 8-hour primary and secondary ambient air quality standards for ozone (O3) is 0.075 parts...

  17. 40 CFR 52.2052 - Motor vehicle emissions budgets for Pennsylvania ozone areas.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... Pennsylvania ozone areas. 52.2052 Section 52.2052 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY...) Pennsylvania § 52.2052 Motor vehicle emissions budgets for Pennsylvania ozone areas. (a) As of December 26... nitrogen oxides (NOX) and volatile organic compounds (VOCs) for the Lancaster 1997 8-Hour Ozone...

  18. 40 CFR 50.15 - National primary and secondary ambient air quality standards for ozone.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... air quality standards for ozone. 50.15 Section 50.15 Protection of Environment ENVIRONMENTAL....15 National primary and secondary ambient air quality standards for ozone. (a) The level of the national 8-hour primary and secondary ambient air quality standards for ozone (O3) is 0.075 parts...

  19. 40 CFR 52.1989 - Interstate Transport for the 1997 8-hour ozone NAAQS and 1997 PM2.5 NAAQS.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Act section 169A and 40 CFR 51.308(e) regarding Best Available Retrofit Technology and the requirements of 40 CFR 51.308(d)(2) and (d)(4)(v) regarding the calculation of baseline and natural conditions... National Park, Diamond Peak Wilderness Area, Three Sisters Wilderness Area, Strawberry Mountain...

  20. 40 CFR 52.1989 - Interstate Transport for the 1997 8-hour ozone NAAQS and 1997 PM2.5 NAAQS.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... Act section 169A and 40 CFR 51.308(e) regarding Best Available Retrofit Technology and the requirements of 40 CFR 51.308(d)(2) and (d)(4)(v) regarding the calculation of baseline and natural conditions... National Park, Diamond Peak Wilderness Area, Three Sisters Wilderness Area, Strawberry Mountain...

  1. 40 CFR 52.1989 - Interstate Transport for the 1997 8-hour ozone NAAQS and 1997 PM2.5 NAAQS.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Act section 169A and 40 CFR 51.308(e) regarding Best Available Retrofit Technology and the requirements of 40 CFR 51.308(d)(2) and (d)(4)(v) regarding the calculation of baseline and natural conditions for the Mt. Hood Wilderness Area, Mt. Jefferson Wilderness Area, Mt Washington Wilderness...

  2. Surface ozone background in the United States: Canadian and Mexican pollution influences

    NASA Astrophysics Data System (ADS)

    Wang, Huiqun; Jacob, Daniel J.; Le Sager, Philippe; Streets, David G.; Park, Rokjin J.; Gilliland, Alice B.; van Donkelaar, A.

    We use a global chemical transport model (GEOS-Chem) with 1° × 1° horizontal resolution to quantify the effects of anthropogenic emissions from Canada, Mexico, and outside North America on daily maximum 8-hour average ozone concentrations in US surface air. Simulations for summer 2001 indicate mean North American and US background concentrations of 26 ± 8 ppb and 30 ± 8 ppb, as obtained by eliminating anthropogenic emissions in North America vs. in the US only. The US background never exceeds 60 ppb in the model. The Canadian and Mexican pollution enhancement averages 3 ± 4 ppb in the US in summer but can be occasionally much higher in downwind regions of the northeast and southwest, peaking at 33 ppb in upstate New York (on a day with 75 ppb total ozone) and 18 ppb in southern California (on a day with 68 ppb total ozone). The model is successful in reproducing the observed variability of ozone in these regions, including the occurrence and magnitude of high-ozone episodes influenced by transboundary pollution. We find that exceedances of the 75 ppb US air quality standard in eastern Michigan, western New York, New Jersey, and southern California are often associated with Canadian and Mexican pollution enhancements in excess of 10 ppb. Sensitivity simulations with 2020 emission projections suggest that Canadian pollution influence in the Northeast US will become comparable in magnitude to that from domestic power plants.

  3. 40 CFR 51.905 - How do areas transition from the 1-hour NAAQS to the 8-hour NAAQS and what are the anti...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... Ambient Air Quality Standard § 51.905 How do areas transition from the 1-hour NAAQS to the 8-hour NAAQS...)(3)(iii) of this section. 40 CFR part 81, subpart C identifies the boundaries of areas and the area... obligations approved into the SIP pursuant to 40 CFR 51.121 and 51.122 may be modified by the State only...

  4. 40 CFR 51.905 - How do areas transition from the 1-hour NAAQS to the 8-hour NAAQS and what are the anti...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... Ambient Air Quality Standard § 51.905 How do areas transition from the 1-hour NAAQS to the 8-hour NAAQS...)(3)(iii) of this section. 40 CFR part 81, subpart C identifies the boundaries of areas and the area... obligations approved into the SIP pursuant to 40 CFR 51.121 and 51.122 may be modified by the State only...

  5. Ozone Layer Observations

    NASA Technical Reports Server (NTRS)

    McPeters, Richard; Bhartia, P. K. (Technical Monitor)

    2002-01-01

    The US National Aeronautics and Space Administration (NASA) has been monitoring the ozone layer from space using optical remote sensing techniques since 1970. With concern over catalytic destruction of ozone (mid-1970s) and the development of the Antarctic ozone hole (mid-1980s), long term ozone monitoring has become the primary focus of NASA's series of ozone measuring instruments. A series of TOMS (Total Ozone Mapping Spectrometer) and SBUV (Solar Backscatter Ultraviolet) instruments has produced a nearly continuous record of global ozone from 1979 to the present. These instruments infer ozone by measuring sunlight backscattered from the atmosphere in the ultraviolet through differential absorption. These measurements have documented a 15 Dobson Unit drop in global average ozone since 1980, and the declines in ozone in the antarctic each October have been far more dramatic. Instruments that measure the ozone vertical distribution, the SBUV and SAGE (Stratospheric Aerosol and Gas Experiment) instruments for example, show that the largest changes are occurring in the lower stratosphere and upper troposphere. The goal of ozone measurement in the next decades will be to document the predicted recovery of the ozone layer as CFC (chlorofluorocarbon) levels decline. This will require a continuation of global measurements of total column ozone on a global basis, but using data from successor instruments to TOMS. Hyperspectral instruments capable of measuring in the UV will be needed for this purpose. Establishing the relative roles of chemistry and dynamics will require instruments to measure ozone in the troposphere and in the stratosphere with good vertical resolution. Instruments that can measure other chemicals important to ozone formation and destruction will also be needed.

  6. The Impact of Emission and Climate Change on Ozone in the United States under Representative Concentration Pathways (RCPs)

    SciTech Connect

    Gao, Yang; Fu, Joshua S.; Drake, John B.; Lamarque, J.-F.; Liu, Yang

    2013-09-27

    Dynamical downscaling was applied in this study to link the global climate-chemistry model Community Atmosphere Model (CAM-Chem) with the regional models: Weather Research and Forecasting (WRF) Model and Community Multi-scale Air Quality (CMAQ). Two Representative Concentration Pathway (RCP) scenarios (RCP 4.5 and RCP 8.5) were used to evaluate the climate impact on ozone concentrations in 2050s. Ozone concentrations in the lower-mid troposphere (surface to ~300 hPa), from mid- to high latitudes in the Northern Hemisphere (NH), show decreasing trends in RCP 4.5 between 2000s and 2050s, with the largest decrease of 4-10 ppbv occurring in the summer and the fall; and increasing trends (2-12 ppbv) in RCP 8.5 resulting from the increased methane emissions. In RCP 8.5, methane emissions increase by ~60% by the end of 2050s, accounting for more than 90% of ozone increases in summer and fall, and 60-80% in spring and winter. Under the RCP 4.5 scenario, in the summer when photochemical reactions are the most active, the large ozone precursor emissions reduction leads to the greatest decrease of downscaled surface ozone concentrations, ranging from 6 to 10 ppbv. However, a few major cities show ozone increases of 3 to 7 ppbv due to weakened NO titration. Under the RCP 8.5 scenario, in winter, downscaled ozone concentrations increase across nearly the entire continental US in winter, ranging from 3 to 10 ppbv due to increased methane emissions and enhanced stratosphere-troposphere exchange (STE). More intense heat waves are projected to occur by the end of 2050s in RCP 8.5, leading to more than 8 ppbv of the maximum daily 8-hour daily average (MDA8) ozone during the heat wave days than other days; this indicates the dramatic impact heat waves exert on high frequency ozone events.

  7. The Impact of Meteorology on Ozone Levels in the Lake Tahoe Basin

    NASA Astrophysics Data System (ADS)

    Theiss, Sandra

    The Lake Tahoe Basin is located on the California-Nevada border and occasionally experiences elevated levels of ozone exceeding the 70 ppb California Air Resources Board (CARB) ambient air quality standard (8-hour average). Previous studies indicate that both the local generation of ozone in the Basin and long-range transport from out-of-Basin sources are important in contributing to ozone exceedances, but little is known about the impact of meteorology on the distribution of ozone source regions. In order to develop a better understanding of the factors affecting ozone levels and sources in the Lake Tahoe Basin, this study combines observational data from a 2010 and 2012 summer field campaigns, HYSPLIT back trajectories, and WRF model output to examine the meteorological influences of ozone transport in the topographically complex Lake Tahoe Basin. Findings from the field work portions of this study include enhanced background ozone levels at higher elevations, the local circulation pattern of lake breezes occurring at Lake level sites, and an indication that ozone precursors are coming off the Lake. Our analysis also showed that if transport of ozone does occur, it is more likely to come from the San Joaquin Valley to the south rather than originate in the large cities to the west, such as Sacramento and San Francisco. Analysis of modeled PBL schemes as compared with observational data showed that the ACM2 PBL scheme best represented the geographical domain. The ACM2 PBL scheme was then used to show wind circulation patterns in the Lake Tahoe Basin and concluded that there is decent vertical mixing over the Basin and no indication of ozone transport from the west however some indication of transport from the east. Overall this study concludes that transport from the west is less significant than transport from the south and east, and that transport only influences ozone values at higher elevations. Within the Basin itself (at lower elevations), local factors

  8. The role of refinery flaring events and bay breezes on a high surface ozone episode during the Houston, Texas DISCOVER-AQ field campaign

    NASA Astrophysics Data System (ADS)

    Loughner, C.; Follette-Cook, M. B.; Fried, A.; Pickering, K. E.

    2015-12-01

    The highest observed surface ozone concentrations in the Houston metropolitan area in 2013 occurred on September 25, which coincided with the Texas DISCOVER-AQ (Deriving Information on Surface Conditions from Column and Vertically Resolved Observations Relevant to Air Quality) field campaign. Surface ozone was elevated throughout the Houston metropolitan area with maximum 8-hour average ozone peaking along the western shore of Galveston Bay, reaching 124 ppbv, almost 50 ppbv above the current EPA standard of 75 ppbv. The NASA P-3B aircraft observed plumes from refinery flares west and northwest of Galveston Bay that were transported over the water. Continental air pollution from the north was transported into the Houston metropolitan area where it mixed with locally generated emissions. A bay breeze circulation formed causing pollutants that were transported out over the water in the morning to recirculate back inland where they mixed with freshly emitted pollution near the bay breeze convergence zone. The highest surface ozone concentrations were reported near the bay breeze front. This ozone episode will be presented using measurements made during the DISCOVER-AQ field campaign and a CMAQ model simulation with integrated source apportionment, which tracks the contribution of emissions source groups and regions on ozone concentrations.

  9. Effects of stratospheric ozone recovery on photochemistry and ozone air quality in the troposphere

    NASA Astrophysics Data System (ADS)

    Zhang, H.; Wu, S.; Huang, Y.; Wang, Y.

    2014-04-01

    There has been significant stratospheric ozone depletion since the late 1970s due to ozone-depleting substances (ODSs). With the implementation of the Montreal Protocol and its amendments and adjustments, stratospheric ozone is expected to recover towards its pre-1980 level in the coming decades. In this study, we examine the implications of stratospheric ozone recovery for the tropospheric chemistry and ozone air quality with a global chemical transport model (GEOS-Chem). With a full recovery of the stratospheric ozone, the projected increases in ozone column range from 1% over the low latitudes to more than 10% over the polar regions. The sensitivity factor of troposphere ozone photolysis rate, defined as the percentage changes in surface ozone photolysis rate for 1% increase in stratospheric ozone column, shows significant seasonal variation but is always negative with absolute value larger than one. The expected stratospheric ozone recovery is found to affect the tropospheric ozone destruction rates much more than the ozone production rates. Significant decreases in surface ozone photolysis rates due to stratospheric ozone recovery are simulated. The global average tropospheric OH decreases by 1.7%, and the global average lifetime of tropospheric ozone increases by 1.5%. The perturbations to tropospheric ozone and surface ozone show large seasonal and spatial variations. General increases in surface ozone are calculated for each season, with increases by up to 0.8 ppbv in the remote areas. Increases in ozone lifetime by up to 13% are found in the troposphere. The increased lifetimes of tropospheric ozone in response to stratospheric ozone recovery enhance the intercontinental transport of ozone and global pollution, in particular for the summertime. The global background ozone attributable to Asian emissions is calculated to increase by up to 15% or 0.3 ppbv in the Northern Hemisphere in response to the projected stratospheric ozone recovery.

  10. 40 CFR 52.1779 - Control strategy: Ozone.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-state Charlotte-Gastonia-Rockhill, North Carolina-South Carolina nonattainment area has attaining data for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR 51.918, suspends the requirements for this area to submit an attainment demonstration, associated reasonably available...

  11. 40 CFR 52.582 - Control strategy: Ozone.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... satisfies 40 CFR 58.20(f) which requires the State to provide for the establishment and maintenance of... area has attaining data for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR... transportation control measures. (1) HOV Lane—This project referred to as AR 073B is the addition of HOV lanes...

  12. Recovery of the Ozone Layer: The Ozone Depleting Gas Index

    NASA Astrophysics Data System (ADS)

    Hofmann, David J.; Montzka, Stephen A.

    2009-01-01

    The stratospheric ozone layer, through absorption of solar ultraviolet radiation, protects all biological systems on Earth. In response to concerns over the depletion of the global ozone layer, the U.S. Clean Air Act as amended in 1990 mandates that NASA and NOAA monitor stratospheric ozone and ozone-depleting substances. This information is critical for assessing whether the Montreal Protocol on Substances That Deplete the Ozone Layer, an international treaty that entered into force in 1989 to protect the ozone layer, is having its intended effect of mitigating increases in harmful ultraviolet radiation. To provide the information necessary to satisfy this congressional mandate, both NASA and NOAA have instituted and maintained global monitoring programs to keep track of ozone-depleting gases as well as ozone itself. While data collected for the past 30 years have been used extensively in international assessments of ozone layer depletion science, the language of scientists often eludes the average citizen who has a considerable interest in the health of Earth's protective ultraviolet radiation shield. Are the ozone-destroying chemicals declining in the atmosphere? When will these chemicals decline to pre-ozone hole levels so that the Antarctic ozone hole might disappear? Will this timing be different in the stratosphere above midlatitudes?

  13. Ozone trends in California`s South Coast Air Basin, 1976--1996

    SciTech Connect

    Cohanim, S.; Cassmassi, J.; Bassett, M.

    1998-12-31

    The South Coast Air Basin (Basin) of Southern California exhibits the worst air quality in the nation, as measured by the annual number of days exceeding the 1-hour National Ambient Air Quality Standard (NAAQS) for ozone. Hourly pollutant concentration data collected by the South Coast Air Quality Management District`s air monitoring network are compared to the existing 1-hour and new 8-hour federal ozone ambient air quality standards to depict ozone trends and compliance in the Basin. Results of trend analyses for the different areas of the Basin are presented for the 1-hour and 8-hour standards, and the relative stringency of the existing and new federal standards is examined. Based on an analysis of the effect of the recently adopted federal standard on ozone compliance in the Basin, ozone concentrations exceed the new federal 8-hour standard level more often than the existing 1-hour standard in most locations. However, examination of the trends in design values for the 1-hour and 8-hour ozone standards suggests that for most locations in the Basin the new standard probably should not be significantly more difficult to attain than the existing standard. The weather-adjusted ozone trend analysis in the Basin confirms the fact that the downtrends in ozone concentrations and number of days exceeding standards are real and independent of annual variation in weather. An analysis of weekday/weekend differences in exceedances for the existing 1-hour and new 8-hour ozone standards show a higher number of days exceeding both standards on weekends for most locations in the Basin, with differences being more evident in the 1990s than in the late 1970s and 1980s

  14. Ozonation of Canadian Athabasca asphaltene

    NASA Astrophysics Data System (ADS)

    Cha, Zhixiong

    Application of ozonation in the petrochemical industry for heavy hydrocarbon upgrading has not been sufficiently explored. Among heavy hydrocarbons, asphaltenes are the heaviest and the most difficult fractions for analysis and treatment. Therefore, ozonation of asphaltenes presents an interesting application in the petrochemical industry. Commercial application of ozonation in the petrochemical industry has three obstacles: availability of an ozone-resistant and environmentally friendly solvent, the precipitation of ozonation intermediates during reaction, and recovery of the solvent and separation of the ozonation products. Preliminary ozonation of Athabasca oil sands asphaltene in nonparticipating solvents encountered serious precipitation of the ozonation intermediates. The precipitated intermediates could be polymeric ozonides and intermolecular ozonides or polymeric peroxides. Because the inhomogeneous reaction medium caused low ozone efficiency, various participating solvents such as methanol and acetic acid were added to form more soluble hydroperoxides. The mass balance results showed that on average, one asphaltene molecule reacted with 12 ozone molecules through the electrophilic reaction and the subsequent decomposition of ozonation intermediates generated acetone extractable products. GC/MS analysis of these compounds indicated that the free radical reactions could be important for generation of volatile products. The extensively ozonated asphaltene in the presence of participating solvents were refluxed with methanol to generate more volatile products. GC/MS analysis of the methanol-esterified ozonation products indicated that most volatile products were aliphatic carboxylic acid esters generated through cleavage of substituents. Reaction kinetics study showed that asphaltene ozonation was initially a diffusion rate-controlled reaction and later developed to a chemical reaction rate-controlled reaction after depletion of the reactive aromatic sites

  15. The role of bay breezes and regional transport on a high surface ozone episode during the Houston, Texas DISCOVER-AQ field campaign

    NASA Astrophysics Data System (ADS)

    Loughner, C.; Follette-Cook, M. B.; Pickering, K. E.; Estes, M. J.

    2014-12-01

    The highest observed surface ozone concentrations in the Houston metropolitan area in 2013 occurred on September 25, which coincided with the Texas DISCOVER-AQ (Deriving Information on Surface Conditions from Column and Vertically Resolved Observations Relevant to Air Quality) field campaign. Surface ozone was elevated throughout the Houston metropolitan area. Maximum 8-hour average ozone peaked along the western shore of Galveston Bay, reaching 124 ppbv, almost 50 ppbv above the current EPA standard of 75 ppbv, at La Porte Sylvan Beach. Continental air pollution from the north and northeast was transported into the Houston metropolitan area where it mixed with locally generated emissions. A bay breeze circulation formed causing pollutants that were transported out over the water in the morning to recirculate back inland where they mixed with freshly emitted pollution near the bay breeze convergence zone. The highest surface ozone concentrations were reported near the bay breeze front at La Porte Sylvan Beach. This ozone episode will be presented using measurements made during the DISCOVER-AQ field campaign and WRF and CMAQ model simulations.

  16. 75 FR 10420 - Approval and Promulgation of Implementation Plans: 1-Hour Ozone Extreme Area Plan for San Joaquin...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-08

    ....'' 57 FR 13498 (April 16, 1992). ARB used its mobile source emissions model EMFAC2002 to generate the on... of Proposed Actions On July 14, 2009 at 74 FR 33933, EPA proposed to approve in part and disapprove...-hour ozone standard). 69 FR 20550 (April 15, 2004). Although we established a new 8-hour ozone...

  17. Unequivocal detection of ozone recovery in the Antarctic Ozone Hole through significant increases in atmospheric layers with minimum ozone

    NASA Astrophysics Data System (ADS)

    de Laat, Jos; van Weele, Michiel; van der A, Ronald

    2015-04-01

    An important new landmark in present day ozone research is presented through MLS satellite observations of significant ozone increases during the ozone hole season that are attributed unequivocally to declining ozone depleting substances. For many decades the Antarctic ozone hole has been the prime example of both the detrimental effects of human activities on our environment as well as how to construct effective and successful environmental policies. Nowadays atmospheric concentrations of ozone depleting substances are on the decline and first signs of recovery of stratospheric ozone and ozone in the Antarctic ozone hole have been observed. The claimed detection of significant recovery, however, is still subject of debate. In this talk we will discuss first current uncertainties in the assessment of ozone recovery in the Antarctic ozone hole by using multi-variate regression methods, and, secondly present an alternative approach to identify ozone hole recovery unequivocally. Even though multi-variate regression methods help to reduce uncertainties in estimates of ozone recovery, great care has to be taken in their application due to the existence of uncertainties and degrees of freedom in the choice of independent variables. We show that taking all uncertainties into account in the regressions the formal recovery of ozone in the Antarctic ozone hole cannot be established yet, though is likely before the end of the decade (before 2020). Rather than focusing on time and area averages of total ozone columns or ozone profiles, we argue that the time evolution of the probability distribution of vertically resolved ozone in the Antarctic ozone hole contains a better fingerprint for the detection of ozone recovery in the Antarctic ozone hole. The advantages of this method over more tradition methods of trend analyses based on spatio-temporal average ozone are discussed. The 10-year record of MLS satellite measurements of ozone in the Antarctic ozone hole shows a

  18. Field Testing of New Interference-Free Ambient Ozone Monitors

    NASA Astrophysics Data System (ADS)

    Ollison, W. M.; Capel, J.; Crow, W.; Johnson, T.; Spicer, C. W.

    2013-05-01

    Multibillion-dollar strategies control ambient air ozone (O3) levels in the U.S. so it is essential that the O3 measurements made for developing state implementation plans, assessing population risks, and determining compliance with regulations be accurate. The predominant U.S. regulatory method employed to monitor ambient O3 is ultraviolet (254 nm) photometry and many previous studies have demonstrated positive interferences associated with this technology. We evaluate two new humidity-controlled commercial instruments - a 2B Technology Model 211 ultraviolet O3 photometer that replaces its conventional MnO2 scrubber with gas-phase NO titration and a Teledyne-API Model 265E NO-O3 chemiluminescence monitor - both designed to minimize the aromatic organic, mercury, and water vapor interferences common to O3 photometers. New units were paired with conventional photometers sampling indoor, outdoor, and in-vehicle environments where populations spend most of their time. Overall, during the fixed-site monitor comparisons in Houston, TX, the three instruments were highly correlated (r2 ≥ 0.99) with regression slopes of 1.00 ± 0.01, and O3 averaged over the study period agreed within 1 ppb; however, U.S. O3 standard compliance depends on fourth highest annual daily maximum 8-hour O3 values, so urban monitors must measure accurately during typically hot, humid, and stagnant O3-conducive day conditions. Conventional photometers reported the highest values for the four highest 8-hour daily maxima during our three month late summer test period, with 8-hour average differences between the new and conventional monitors ranging up to 4 ppb. In paired 10-minute average sampling with a Model 211 in Durham, NC, conventional photometers generally exhibited modest positive interference bias (under 5 ppb) in 176 sampled residences, shops, malls, restaurants, offices, parks, roadways, and vehicles; however, in six percent of our samples indoor differences exceeded 10 ppb and in two

  19. Tropospheric ozone in the vicinity of the ozone hole - 1987 Airborne Antarctic Ozone Experiment

    NASA Technical Reports Server (NTRS)

    Gregory, Gerald L.; Warren, Linda S.; Hypes, Warren D.; Tuck, Adrian F.; Kelly, Kenneth K.; Krueger, Arlin J.

    1989-01-01

    Results are presented on ozone measurements in the upper troposphere/lower stratosphere over Antarctica, obtained by NASA DC-8 aircraft during the August/September 1987 Airborne Antarctic Ozone Experiment. The ozone mixing ratios as high as several hundred ppbv were measured, but in all cases these ratios were observed in pockets of upper atmospheric air, both in the vicinity of and away from the location of the ozone hole. The background ozone values in the surrounding troposphere were typically in the range of 20-50 ppbv. Correlation of tropospheric ozone observations with the boundaries of the ozone hole differed in the course of the experiment. During the August 28 - September 2 flights, encounters with ozone-rich air were limited, and the background tropospheric ozone appeared to decrease beneath the hole. For the later flights, and as the ozone hole deepened, the ozone-rich air was frequently observed in the vicinity of the hole, and the average ozone values at the flight altitude were frequently higher than the background values.

  20. Tropospheric ozone in the vicinity of the ozone hole: 1987 Airborne Antarctic Ozone Experiment

    SciTech Connect

    Gregory, G.L.; Warren, L.S. ); Hypes, W.D. ); Tuck, A.F.; Kelly, K.K. ); Krueger, A.J. )

    1989-11-30

    Tropospheric ozone measurements over Antarctica aboard the NASA DC-8 aircraft are summarized. As part of the August/September 1987 Airborne Antarctic Ozone Experiment, the aircraft flew 13 missions covering a latitude of 53{degree}-90{degree}S, at altitudes to 13 km. Ozone mixing ratios as high as several hundred parts per billion by volume (ppbv) were measured, but in all cases these ratios were observed in pockets or patches of upper atmospheric air. These pockets were observed both in the vicinity of and away from the location of the ozone hole. At times, and as a result of these pockets, the ozone levels at the flight altitude of the aircraft, as averaged beneath the boundaries of the stratospheric ozone hole, were 2-3 times higher than background tropospheric values. The data suggest that the ozone-rich air seldom penetrated below about 9-km altitude. Background ozone values in the surrounding troposphere were typically in the range of 20-50 ppbv. Correlation of tropospheric ozone observations with the boundaries of the ozone hole differed during the experiment. During the early flights (August 28 through September 2), encounters with ozone-rich air were limited and background tropospheric ozone (at the flight altitude) appeared to decrease beneath the hole. For many of the later flights, and as the hole deepened, the reverse was noted, in that ozone-rich air was frequently observed in the vicinity of the hole and, as noted earlier, average ozone at the flight altitude was frequently higher than background values.

  1. Alteration in carboxyhemoglobin concentrations during exposure to 9 ppm carbon monoxide for 8 hours at sea level and 2134 m altitude in a hypobaric chamber

    SciTech Connect

    Horvath, S.M.; Bedi, J.F. )

    1989-10-01

    Seventeen non-smoking young men served as subjects to determine the alteration in carboxyhemoglobin (COHb) concentrations during exposure to 0 or 9 ppm carbon monoxide for 8 hours (CO) at sea level or an altitude of 2134 meters (7000 feet) in a hypobaric chamber. Nine subjects rested during the exposure and 8 exercised for 10 minutes of each exposure hour at a mean ventilation of 25 L (BTPS). All subjects performed a maximal aerobic capacity test at the completion of their respective exposures. Carboxyhemoglobin concentrations fell in all subjects during their exposures to 0 ppm CO at sea level or 2134 m. During the 8-h exposures to 9 ppm CO, COHb rose linearly from approximately 0.2 percent to 0.7 percent. No significant differences in uptake were found whether the subjects were resting or intermittently exercising during their 8-h exposures. COHb levels attained were similar at both sea level and 2134 m. Maximal aerobic capacity was reduced approximately 7-10 percent consequent to altitude exposure during 0 ppm CO exposures. These values were not altered following exposure for 8 h to 9 ppm CO in either the resting or exercising subjects.

  2. Quaternion Averaging

    NASA Technical Reports Server (NTRS)

    Markley, F. Landis; Cheng, Yang; Crassidis, John L.; Oshman, Yaakov

    2007-01-01

    Many applications require an algorithm that averages quaternions in an optimal manner. For example, when combining the quaternion outputs of multiple star trackers having this output capability, it is desirable to properly average the quaternions without recomputing the attitude from the the raw star tracker data. Other applications requiring some sort of optimal quaternion averaging include particle filtering and multiple-model adaptive estimation, where weighted quaternions are used to determine the quaternion estimate. For spacecraft attitude estimation applications, derives an optimal averaging scheme to compute the average of a set of weighted attitude matrices using the singular value decomposition method. Focusing on a 4-dimensional quaternion Gaussian distribution on the unit hypersphere, provides an approach to computing the average quaternion by minimizing a quaternion cost function that is equivalent to the attitude matrix cost function Motivated by and extending its results, this Note derives an algorithm that deterniines an optimal average quaternion from a set of scalar- or matrix-weighted quaternions. Rirthermore, a sufficient condition for the uniqueness of the average quaternion, and the equivalence of the mininiization problem, stated herein, to maximum likelihood estimation, are shown.

  3. Smoke in the City: How Often and Where Does Smoke Impact Summertime Ozone in the United States?

    NASA Astrophysics Data System (ADS)

    Brey, S. J.; Fischer, E. V.

    2015-12-01

    The mechanisms and magnitude of the contribution of fires to ozone (O3) production is poorly understood. In this work we investigate the influence of fire on O3 abundances over the contiguous United States. Using co-located observations of particulate matter (PM2.5) and the National Weather Service Hazard Mapping System smoke data, we identify summertime days between 2005 and 2014 that Environmental Protection Agency (EPA) Air Quality System (AQS) O3 monitors are influenced by smoke. We then compare O3 mixing ratio distributions for smoke-free and smoke-impacted days for each O3 monitor. We observe that the mean O3 abundance measured on smoke-impacted days is higher than on smoke-free days. The magnitude of the effect varies by location with a range of 0 to 37 parts per billion by volume (ppbv). We find that smoke is present on a non-negligible proportion of days when the 8-hour average O3 mixing ratio exceeds the EPA limit of 75 ppbv in regions and locations with significant O3 issues, including the Northeast urban corridor, Dallas, Houston, Atlanta, Birmingham, and Kansas City. Most U.S. cities maintain a similar proportion of smoke-impacted exceedence days when they are held against a more stringent limit of 65 ppbv for an 8-hour average. We show that smoke-impacted O3 mixing ratios are most elevated in U.S. cities with the highest emissions of nitrogen oxides (NOX).

  4. Calculations of Polar Ozone Loss Rates

    NASA Technical Reports Server (NTRS)

    Dessler, A. E.; Wu, J.

    1999-01-01

    We calculate vortex-averaged ozone loss rates at 465-K potential temperature during the Aug.-Sept. time period in the southern hemisphere and Feb.-Mar. time period in the northern hemisphere. Ozone loss rates are calculated two ways. First, from the time series of measurements of 03. Second, from measurements of ClO, from which ozone loss is inferred based on our theories of Cl-catalyzed ozone destruction. Both measurement sets are from the Upper Atmosphere Research Satellite (UARS) Microwave Limb Sounder (MLS) instrument. We find good agreement between vortex-averaged ozone loss rates calculated from these methods. Our analysis provides no support for recent work suggesting that current theories of Cl-catalyzed ozone loss underestimate the observed decrease in polar ozone during the ozone "hole" period.

  5. The 1990 Antarctic ozone hole as observed by TOMS. [Total Ozone Mapping Spectrometer

    SciTech Connect

    Newman, P.; Stolarski, R.; Schoeberl, M.; McPeters, R.; Krueger, A.

    1991-04-01

    The 1990 Antarctic ozone hole matched the record 1987 ozone hole in depth, duration, and area. During the formation phase of the hole (August), total ozone values were the lowest yet recorded. The decline rate approximately matched the record 1987 decline, and reached a minimum of 125 Dobson Units on October 4, 1990. October total ozone averages were marginally higher than 1987. As during 1987, the 1990 total ozone values within the hole slowly and steadily increased during the mid-October through November period. The ozone hole breakup was the latest yet recorded (early December), with low ozone values persisting over the pole through December, setting a record low for December average polar ozone. Temperatures were near average during the early spring, but were below normal for the late-spring. Temperatures in the early spring of 1990 were substantially warmer than those observed in the early spring of 1987.

  6. The 1990 Antarctica ozone hole as observed by TOMS. [Total Ozone Mapping Spectrometer

    NASA Technical Reports Server (NTRS)

    Newman, Paul; Stolarski, Richard; Schoeberl, Mark; Mcpeters, Richard; Krueger, Arlin

    1991-01-01

    The 1990 Antarctic ozone hole matched the record 1987 ozone hole in depth, duration, and area. During the formation phase of the hole (August), total ozone values were the lowest yet recorded. The decline rate approximately matched the record 1987 decline and reached a minimum of 125 Dobson Units on October 4, 1990. October total ozone averages were marginally higher that 1987. As during 1987, the 1990 total ozone values within the hole slowly and steadily increased during the mid-October through November period. The ozone hole breakup was the latest yet recorded (early December), with low ozone values persisting over the pole through December, setting a record low for December average polar ozone. Temperatures were near average during the early spring, but were below normal for the late spring. Temperatures in the early spring of 1990 were substantially warmer than those observed in the early spring of 1987.

  7. Impact of downward-mixing ozone on surface ozone accumulation in southern Taiwan.

    PubMed

    Lin, Ching-Ho

    2008-04-01

    The ozone that initially presents in the previous day's afternoon mixing layer can remain in the nighttime atmosphere and then be carried over to the next morning. Finally, this ozone can be brought to the ground by downward mixing as mixing depth increases during the daytime, thereby increasing surface ozone concentrations. Variation of ozone concentration during each of these periods is investigated in this work. First, ozone concentrations existing in the daily early morning atmosphere at the altitude range of the daily maximum mixing depth (residual ozone concentrations) were measured using tethered ozonesondes on 52 experimental days during 2004-2005 in southern Taiwan. Daily downward-mixing ozone concentrations were calculated by a box model coupling the measured daily residual ozone concentrations and daily mixing depth variations. The ozone concentrations upwind in the previous day's afternoon mixing layer were estimated by the combination of back air trajectory analysis and known previous day's surface ozone distributions. Additionally, the relationship between daily downward-mixing ozone concentration and daily photochemically produced ozone concentration was examined. The latter was calculated by removing the former from daily surface maximum ozone concentration. The measured daily residual ozone concentrations distributed at 12-74 parts per billion (ppb) with an average of 42 +/- 17 ppb are well correlated with the previous upwind ozone concentration (R2 = 0.54-0.65). Approximately 60% of the previous upwind ozone was estimated to be carried over to the next morning and became the observed residual ozone. The daily downward-mixing ozone contributes 48 +/- 18% of the daily surface maximum ozone concentration, indicating that the downward-mixing ozone is as important as daily photochemically produced ozone to daily surface maximum ozone accumulation. The daily downward-mixing ozone is poorly correlated with the daily photochemically produced ozone and

  8. Interannual Variability in Baseline Ozone and Its Relationship to Surface Ozone in the Western U.S.

    PubMed

    Baylon, Pao M; Jaffe, Daniel A; Pierce, R Bradley; Gustin, Mae S

    2016-03-15

    Baseline ozone refers to observed concentrations of tropospheric ozone at sites that have a negligible influence from local emissions. The Mount Bachelor Observatory (MBO) was established in 2004 to examine baseline air masses as they arrive to North America from the west. In May 2012, we observed an O3 increase of 2.0-8.5 ppbv in monthly average maximum daily 8-hour average O3 mixing ratio (MDA8 O3) at MBO and numerous other sites in the western U.S. compared to previous years. This shift in the O3 distribution had an impact on the number of exceedance days. We also observed a good correlation between daily MDA8 variations at MBO and at downwind sites. This suggests that under specific meteorological conditions, synoptic variation in O3 at MBO can be observed at other surface sites in the western U.S. At MBO, the elevated O3 concentrations in May 2012 are associated with low CO values and low water vapor values, consistent with transport from the upper troposphere/lower stratosphere (UT/LS). Furthermore, the Real-time Air Quality Modeling System (RAQMS) analyses indicate that a large flux of O3 from the UT/LS in May 2012 contributed to the observed enhanced O3 across the western U.S. Our results suggest that a network of mountaintop observations, LiDAR and satellite observations of O3 could provide key data on daily and interannual variations in baseline O3. PMID:26882468

  9. Protecting beans from ozone

    SciTech Connect

    Pierce, R.

    1983-03-01

    A chemical treatment to protect navy beans from ozone damage increased yields by an average of more than 20% in 3 years of tests. An experimental antioxidant chemical, EDU, made by the DuPont company was tested as soil applications and sprays on several varieties and under a variety of soil and planting conditions. The average yield increases were between 16 and 24%. Chemical treatment also increased snap bean pod production by 12%.

  10. Chemistry and Dynamics of the Unusual 2015 Antarctic Ozone Hole

    NASA Astrophysics Data System (ADS)

    Braathen, Geir O.

    2016-04-01

    The Global Atmosphere Watch of the World Meteorological Organization includes several stations in Antarctica that keep a close eye on the ozone layer during the ozone hole season. Observations made during the unusually large ozone hole of 2015 will be compared to ozone holes from 2003 to 2014 and interpreted in light of the meteorological conditions. Satellite observations will be used to get a more general picture of the size and depth of the ozone hole and will also be used to calculate various metrics for ozone hole severity. In 2003, 2005 and 2006, the ozone hole was relatively large with more ozone loss than normal. This is in particular the case for 2006, which by most ozone hole metrics was the most severe ozone hole on record. On the other hand, the ozone holes of 2004, 2007, 2010 and 2012, 2013 and 2014 were less severe than normal, and only the very special ozone hole of 2002 had less ozone depletion when one regards the ozone holes of the last decade. The South Polar vortex of 2015 was unusually stable and long-lived, so ozone depletion lasted longer than seen in recent years. The ozone hole area, i.e. the area where total ozone is less that 220 DU, averaged over the worst 60 consecutive days was larger in 2015 than in any other year since the beginning of the ozone hole era in the early 1980s.

  11. 78 FR 9596 - Approval and Promulgation of Implementation Plans; New Jersey and New York Ozone Attainment...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-11

    ... attainment of the 1997 8-hour ozone NAAQS during this monitoring period. See 77 FR 36163, 77 FR 47533, 77 FR 17341, and 74 FR 63993. EPA is aware that preliminary ambient air quality monitoring data for 2012 may... moderate nonattainment areas. On December 11, 2012 (77 FR 73570), EPA published a notice of...

  12. 78 FR 21302 - Approval and Promulgation of Implementation Plans; New York State Ozone Implementation Plan Revision

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-04-10

    ... outdoors, and individuals with a pre-existing respiratory disease, such as asthma. On April 30, 2004 (69 FR... a requirement to submit a demonstration of attainment. EPA notes that on December 7, 2009 (74 FR..., 2008 (73 FR 15672) EPA determined that Jefferson County attained the 8-hour ozone standard. On June...

  13. 76 FR 77178 - Approval and Promulgation of Implementation Plans; New York State Ozone Implementation Plan Revision

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-12

    ... individuals with a pre-existing respiratory disease, such as asthma. On April 30, 2004 (69 FR 23858), EPA... Poughkeepsie nonattainment area is composed of Dutchess, Orange and Putnam counties. On December 7, 2009 (74 FR 63993), EPA determined that the Poughkeepsie area attained the 8-hour ozone standard and on March...

  14. 77 FR 26950 - Designation of Areas for Air Quality Planning Purposes; California; Western Mojave Desert Ozone...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-05-08

    ...'' nonattainment for the 1997 8-hour ozone NAAQS.\\1\\ See 69 FR 23858, at 23884 (April 30, 2004) and 40 CFR 81.305... FR 29073, May 20, 2008), and reclassified the Sacramento Metro area from ``Serious'' to ``Severe-15'' nonattainment effective June 4, 2010 (75 FR 24409, May 5, 2010). \\3\\ CARB subsequently submitted a SIP...

  15. 78 FR 7672 - Approval and Promulgation of Implementation Plans; Texas; Beaumont/Port Arthur Ozone Maintenance...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-04

    ... Vehicle Emissions Simulator (MOVES) 2010a emissions model. The BPA 1997 8-hour ozone maintenance area... index, some information is not publicly available, e.g., Confidential Business Information or other... at the Air Planning Section (6PD-L), Environmental Protection Agency, 1445 Ross Avenue, Suite...

  16. Improved Space-Time Forecasting of next Day Ozone Concentrations in the Eastern U.S.

    EPA Science Inventory

    There is an urgent need to provide accurate air quality information and forecasts to the general public and environmental health decision-makers. This paper develops a hierarchical space-time model for daily 8-hour maximum ozone concentration (O3) data covering much of the easter...

  17. 76 FR 48207 - Federal Implementation Plans: Interstate Transport of Fine Particulate Matter and Ozone and...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-08-08

    ... FIP Federal Implementation Plan FR Federal Register EPA U.S. Environmental Protection Agency GHG... proposed revisions to the 8-hour ozone NAAQS that the Agency had issued March 12, 2008 (75 FR 2938); the... the District of Columbia Circuit (``Court'') in 2008. CAIR, promulgated May 12, 2005 (70 FR...

  18. Identifying and forecasting deep stratospheric ozone intrusions over the western United States from space

    NASA Astrophysics Data System (ADS)

    Lin, M.; Fiore, A. M.; Horowitz, L. W.; Cooper, O. R.; Langford, A. O.; Pan, L.; Liu, X.; Reddy, P. J.

    2012-12-01

    Recent studies have shown that deep stratospheric ozone intrusions can episodically enhance ground-level ozone above the health-based standard over the western U.S. in spring. Advanced warning of incoming intrusions could be used by state agencies to inform the public about poor air quality days. Here we explore the potential for using total ozone retrievals (version 5.2, level 3) at twice daily near global coverage from the AIRS instrument aboard the NASA Aqua satellite to identify stratospheric intrusions and forecast the eventual surface destination of transported stratospheric ozone. The method involves the correlation of AIRS daily total ozone columns at each 1ox1o grid box ~1-3 days prior to stratospheric enhancements to daily maximum 8-hour average ozone at a selected surface site using datasets from April to June in 2003-2011. The surface stratospheric enhancements are estimated by the GFDL AM3 chemistry-climate model which includes full stratospheric and tropospheric chemistry and is nudged to reanalysis winds. Our earlier work shows that the model presents deep stratospheric intrusions over the Western U.S. consistently with observations from AIRS, surface networks, daily ozone sondes, and aircraft lidar available in spring of 2010 during the NOAA CalNex field campaign. For the 15 surface sites in the U.S. Mountain West considered, a correlation coefficient of 0.4-0.7 emerges with AIRS ozone columns over 30o-50oN latitudes and 125o-105oW longitudes - variability in the AIRS column within this spatial domain indicates incoming intrusions. For each "surface receptor site", the spatial domain can narrow to an area ~5ox5o northwest of the individual site, with the strong correlation (0.5-0.7) occurring when the AIRS data is lagged by 1 day from the AM3 stratospheric enhancements in surface air. The spatial pattern of correlations is consistent with our process-oriented understanding developed from case studies of extreme intrusions. Surface observations

  19. Ozone decomposition

    PubMed Central

    Batakliev, Todor; Georgiev, Vladimir; Anachkov, Metody; Rakovsky, Slavcho

    2014-01-01

    Catalytic ozone decomposition is of great significance because ozone is a toxic substance commonly found or generated in human environments (aircraft cabins, offices with photocopiers, laser printers, sterilizers). Considerable work has been done on ozone decomposition reported in the literature. This review provides a comprehensive summary of the literature, concentrating on analysis of the physico-chemical properties, synthesis and catalytic decomposition of ozone. This is supplemented by a review on kinetics and catalyst characterization which ties together the previously reported results. Noble metals and oxides of transition metals have been found to be the most active substances for ozone decomposition. The high price of precious metals stimulated the use of metal oxide catalysts and particularly the catalysts based on manganese oxide. It has been determined that the kinetics of ozone decomposition is of first order importance. A mechanism of the reaction of catalytic ozone decomposition is discussed, based on detailed spectroscopic investigations of the catalytic surface, showing the existence of peroxide and superoxide surface intermediates. PMID:26109880

  20. Ozone decomposition.

    PubMed

    Batakliev, Todor; Georgiev, Vladimir; Anachkov, Metody; Rakovsky, Slavcho; Zaikov, Gennadi E

    2014-06-01

    Catalytic ozone decomposition is of great significance because ozone is a toxic substance commonly found or generated in human environments (aircraft cabins, offices with photocopiers, laser printers, sterilizers). Considerable work has been done on ozone decomposition reported in the literature. This review provides a comprehensive summary of the literature, concentrating on analysis of the physico-chemical properties, synthesis and catalytic decomposition of ozone. This is supplemented by a review on kinetics and catalyst characterization which ties together the previously reported results. Noble metals and oxides of transition metals have been found to be the most active substances for ozone decomposition. The high price of precious metals stimulated the use of metal oxide catalysts and particularly the catalysts based on manganese oxide. It has been determined that the kinetics of ozone decomposition is of first order importance. A mechanism of the reaction of catalytic ozone decomposition is discussed, based on detailed spectroscopic investigations of the catalytic surface, showing the existence of peroxide and superoxide surface intermediates. PMID:26109880

  1. Polar ozone

    NASA Technical Reports Server (NTRS)

    Solomon, S.; Grose, W. L.; Jones, R. L.; Mccormick, M. P.; Molina, Mario J.; Oneill, A.; Poole, L. R.; Shine, K. P.; Plumb, R. A.; Pope, V.

    1990-01-01

    The observation and interpretation of a large, unexpected ozone depletion over Antarctica has changed the international scientific view of stratospheric chemistry. The observations which show the veracity, seasonal nature, and vertical structure of the Antarctic ozone hole are presented. Evidence for Arctic and midlatitude ozone loss is also discussed. The chemical theory for Antarctic ozone depletion centers around the occurrence of polar stratospheric clouds (PSCs) in Antarctic winter and spring; the climatology and radiative properties of these clouds are presented. Lab studies of the physical properties of PSCs and the chemical processes that subsequently influence ozone depletion are discussed. Observations and interpretation of the chemical composition of the Antarctic stratosphere are described. It is shown that the observed, greatly enhanced abundances of chlorine monoxide in the lower stratosphere are sufficient to explain much if not all of the ozone decrease. The dynamic meteorology of both polar regions is given, interannual and interhemispheric variations in dynamical processes are outlined, and their likely roles in ozone loss are discussed.

  2. Ozone decomposition.

    PubMed

    Batakliev, Todor; Georgiev, Vladimir; Anachkov, Metody; Rakovsky, Slavcho; Zaikov, Gennadi E

    2014-06-01

    Catalytic ozone decomposition is of great significance because ozone is a toxic substance commonly found or generated in human environments (aircraft cabins, offices with photocopiers, laser printers, sterilizers). Considerable work has been done on ozone decomposition reported in the literature. This review provides a comprehensive summary of the literature, concentrating on analysis of the physico-chemical properties, synthesis and catalytic decomposition of ozone. This is supplemented by a review on kinetics and catalyst characterization which ties together the previously reported results. Noble metals and oxides of transition metals have been found to be the most active substances for ozone decomposition. The high price of precious metals stimulated the use of metal oxide catalysts and particularly the catalysts based on manganese oxide. It has been determined that the kinetics of ozone decomposition is of first order importance. A mechanism of the reaction of catalytic ozone decomposition is discussed, based on detailed spectroscopic investigations of the catalytic surface, showing the existence of peroxide and superoxide surface intermediates.

  3. Impact of biogenic emissions on ozone and fine particles over Europe: Assessing the effect of temperature increase and the role of anthropogenic NOx emissions reduction

    NASA Astrophysics Data System (ADS)

    Tagaris, Efthimios; Sotiropoulou, Rafaella-Eleni P.; Gounaris, Nikos; Andronopoulos, Spyros; Vlachogiannis, Diamando

    2014-05-01

    The role of biogenic emissions on ozone and PM2.5 levels over Europe is assessed for July 2006 using the CMAQ modeling system. Biogenic emissions are simulated to increase the daily maximum 8 hour ozone (Max8hrO3) mixing ratios and to decrease PM2.5 average concentrations over Europe. Since climate change will lead to higher temperatures increasing subsequently biogenic emissions, sensitivity analysis to temperature is performed. Higher temperatures suggest an average increase in Max8hrO3 mixing ratios over Europe by about 3% and an average decrease in PM2.5 concentrations by about 6%, related to a temperature increase by 3 K degrees. Temperature increases are simulated, also, to increase the organic part of PM2.5 and to decrease the inorganic one on average over Europe. In order to examine if abatement measures for anthropogenic emissions could offset ozone increases in a warmer environment and their effect on PM2.5 concentrations, simulation with a domain wide reduction of anthropogenic NOx emissions by 10% is performed. This is estimated to reduce Max8hrO3 mixing ratios on average over Europe, however, in VOCs limited areas there is an increase. The reduction in anthropogenic NOx emissions is simulated to reduce PM2.5 concentrations on average over Europe enhancing the reduction simulated in a warmer environment but further modifying PM2.5 component concentrations. This work was supported by the National Strategic Reference Framework (NSRF) 2007-2013 grand No 09SYN-31-667.

  4. Selected Measurements of Total Arctic Column Ozone Amounts from Aura's Ozone Monitoring Instrument,

    NASA Technical Reports Server (NTRS)

    2005-01-01

    Images from Aura's Ozone Monitoring Instrument showing the average total column ozone during the months of January and March, and the total column ozone on the single day of 11 March. Although there was near record chemical ozone loss between January and March, comparing the January and March images shows that on average the lowest total column ozone values in polar regions are slightly higher in March than in January. This is because of the other process that brought higher ozone into the vortex region, thus compensating for the very significant chemical loss. The 11 March image shows that, despite the unremarkable overall March values, on an individual day, chemical loss and dynamical processes combined to result in localized regions of much lower ozone (which resulted in higher UV exposure at the Earth's surface for individual days and places).

  5. Ozone variability

    NASA Astrophysics Data System (ADS)

    Duetsch, H. U.

    1983-09-01

    The annual and long-term variations in the atmospheric ozone layer were examined on the basis of 55 yr of data taken at Aroya, Switzerland and 25 yr of data gathered by the global ozone network. Attention was given to annual and biennial variations, which showed that the midlatitude peak concentration was affected by a quasi-biennial variation of the tropical stratospheric circulation. Smaller scale circulation patterns were dominant in the lower stratosphere, although an observed negative trend of the total ozone was equally distributed between the troposphere and 24 km altitude. The global ozone increase detected in the 1960s was possible due to general circulation alterations, but may also have been influenced by injection of NO(x) into the atmosphere during atomic bomb testing.

  6. Ozone, Tropospheric

    NASA Technical Reports Server (NTRS)

    Fishman, Jack

    1995-01-01

    In the early part of the 20th century, ground-based and balloon-borne measurements discovered that most of atmosphere's ozone is located in the stratosphere with highest concentrations located between 15 and 30 km (9,3 and 18.6 miles). For a long time, it was believed that tropospheric ozone originated from the stratosphere and that most of it was destroyed by contact with the earth's surface. Ozone, O3, was known to be produced by the photo-dissociation of molecular oxygen, O2, a process that can only occur at wavelengths shorter than 242 nm. Because such short-wave-length radiation is present only in the stratosphere, no tropospheric ozone production is possible by this mechanism. In the 1940s, however, it became obvious that production of ozone was also taking place in the troposphere. The overall reaction mechanism was eventually identified by Arie Haagen-Smit of the California Institute of Technology, in highly polluted southern California. The copious emissions from the numerous cars driven there as a result of the mass migration to Los Angeles after World War 2 created the new unpleasant phenomenon of photochemical smog, the primary component of which is ozone. These high levels of ozone were injuring vegetable crops, causing women's nylons to run, and generating increasing respiratory and eye-irritation problems for the populace. Our knowledge of tropospheric ozone increased dramatically in the early 1950s as monitoring stations and search centers were established throughout southern California to see what could be done to combat this threat to human health and the environment.

  7. Is There an Arctic Ozone Hole?

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.

    2000-01-01

    Total ozone observations from the Total Ozone Mapping Spectrometer (TOMS) instruments during March 1997 revealed an extensive region of low column densities in the Arctic region centered near the north pole. Values were below 250 Dobson units for nearly a two week period during this period, and were correlated with the position of the northern lower stratospheric polar vortex. The March 1997 average total ozone column densities were more than 30% lower than the average of column densities observed during the 1979-1982 March period. Both the northern spring seasons of 1998 and 1999 have shown much higher levels of total ozone. In this presentation, we will discuss the causes of the low total ozone values in 1997 and contrast those low values with the higher 1998 and 1999 observations. I will additionally discuss the just completed SOLVE campaign and the March 2000 ozone values.

  8. Lower tropospheric ozone and aerosol measurements at a coastal mountain site in Central California

    NASA Astrophysics Data System (ADS)

    Post, A.; Faloona, I. C.; Lighthall, D.; Wexler, A. S.; Cliff, S. S.; Conley, S. A.; Zhao, Y.

    2013-12-01

    Increasing concern over the impacts of exogenous air pollution in California's Central Valley has prompted the establishment of a coastal, high altitude monitoring site at the Chews Ridge Observatory (1550 m) approximately 30 km east of Point Sur in Monterey County, operated by the Monterey Institute for Research in Astronomy. Eighteen months of ozone and aerosol measurements are presented in the context of long-range transport and its potential impact on surface air quality in the southern San Joaquin Valley. Moreover, several ozone surveys have been conducted by aircraft upwind, over the Pacific Ocean, and downwind, over the Central Valley, to characterize horizontal and vertical transport across the coastal mountains. Diurnal variations present at Chews Ridge indicate the formation of a convective boundary layer on the ridge during the daytime leading to a 6-8 ppb decrease in ozone accompanied by a rise in specific humidity of 2-3 g/kg due to coupling with the forest. During the nighttime, the sampled air masses are representative of free tropospheric conditions which have not been significantly influenced by either local emissions nor convective coupling to the surface. The maximum daily 8-hour average ozone concentration at Chews Ridge is used in lagged correlation analysis with two sites in the San Joaquin Valley, Fresno and Arvin, to de-emphasize the influence of locally produced, diurnally cycled ozone. The correlation coefficients (~0.60) peak between 9-21 hour lag and tend to decorrelate completely within 4-5 days. These and other analyses along with data provided by the aircraft sampling are used to provide a deeper understanding of ozone transport into the San Joaquin Valley. Aerosol size is measured with a scanning mobility particle sizer and composition is analyzed with an 8-stage rotating drum impactor whose substrates are characterized by X-ray fluorescence. Various elemental ratios and back trajectory calculations are used to infer the temporal

  9. The threee-dimensional morphology of the Antarctic ozone hole

    NASA Technical Reports Server (NTRS)

    Aikin, Arthur C.; Mcpeters, R. D.

    1988-01-01

    The three-dimensional morphology of the spring antarctic ozone distribution as determined by the Nimbus 7 Solar Backscatter Ultraviolet (SBUV) spectrometer instrument is presented for the period 1 to 11 October in 1986. The data show that a clearly defined minimum in ozone relative to the local ozone field extends throughout the stratosphere from the tropopause to above 50 km, though decreasing in intensity with altitude. Near 18 km ozone in the ozone hole is 50 percent less than the average surrounding ozone. But even at 50 km the ozone is 20 percent less than the surrounding ozone field. The ozone minimum in the upper stratosphere is displaced about 6 degrees toward the equator so that observations at a fixed station may provide the illusion that the ozone minimum is restricted only to low altitudes. While the ozone minimum is spatially coherent throughout the stratosphere, there are differences in the behavior of ozone at different altitudes that suggest the existence of at least three distinct altitude domains. Below 30 km ozone is characterized by classic ozone hole behavior. Between 33 and 43 km ozone is more stable, actually increasing during September and October. Above 43 km ozone has always decreased during September to a minimum in October, but it has suffered a long term decrease of 7 to 12 percent since 1979 similar to that seen at low altitudes.

  10. Options to accelerate ozone recovery: ozone and climate benefits

    NASA Astrophysics Data System (ADS)

    Daniel, J. S.; Fleming, E. L.; Portmann, R. W.; Velders, G. J. M.; Jackman, C. H.; Ravishankara, A. R.

    2010-08-01

    Hypothetical reductions in future emissions of ozone-depleting substances (ODSs) and N2O are evaluated in terms of effects on equivalent effective stratospheric chlorine (EESC), globally-averaged total column ozone, and radiative forcing through 2100. Due to the established success of the Montreal Protocol, these actions can have only a fraction of the impact on ozone depletion that regulations already in force have had. If all anthropogenic ODS and N2O emissions were halted beginning in 2011, ozone is calculated to be higher by about 1-2% during the period 2030-2100 compared to a case of no additional restrictions. Direct radiative forcing by 2100 would be about 0.23 W/m2 lower from the elimination of anthropogenic N2O emissions and about 0.005 W/m2 lower from the destruction of the chlorofluorocarbon (CFC) bank. Due to the potential impact of N2O on future ozone levels, we provide an approach to incorporate it into the EESC formulation, which is used extensively in ozone depletion analyses. The ability of EESC to describe total ozone changes arising from additional ODS and N2O controls is also quantified.

  11. Trends in ozone profile measurements

    NASA Technical Reports Server (NTRS)

    Johnston, H.; Aikin, A.; Barnes, R.; Chandra, S.; Cunnold, D.; Deluisi, J.; Gille, J. C.; Hudson, R.; Mccormick, M. P.; Mcmaster, L.

    1989-01-01

    From an examination of the agreements and differences between different satellite instruments, it is difficult to believe that existing satellite instruments determine upper stratospheric ozone much better than 4 pct.; by extension, it probably would require at least a 4 pct. change to be reliably detected as a change. The best estimates of the vertical profiles of ozone change in the upper stratosphere between 1979 and 1986 are judged to be those given by the two SAGE satellite instruments. SAGE-2 minus SAGE-1 gives a much lower ozone reduction than that given by the archived Solar Backscatter UV data. The average SAGE profiles of ozone changes between 20 and 50 degs north and between 20 and 50 degs south are given. The SAGE-1 and SAGE-2 comparison gives an ozone reduction of about 4 pct. at 25 km over temperate latitudes. Five ground based Umkehr stations between 36 and 52 degs north, corrected for the effects of volcanic aerosols, report an ozone reduction between 1979 and 1987 at Umkehr layer 8 of 9 + or - 5 pct. The central estimate of upper stratospheric ozone reduction given by SAGE at 40 km is less than the central value estimated by the Umkehr method at layer 8.

  12. Effects of Ozone and Peroxyacetyl Nitrate on Polar Lipids and Fatty Acids in Leaves of Morning Glory and Kidney Bean

    PubMed Central

    Nouchi, Isamu; Toyama, Susumu

    1988-01-01

    To compare the effects of ozone and peroxyacetyl nitrate (PAN) on leaf lipids, fatty acids and malondialdehyde (MDA), morning glory (Pharbitis nil Choisy cv Scarlet O'Hara) and kidney bean (Phaseolus vulgaris L. cv Gintebo) plants were exposed to either ozone (0.15 microliter per liter for 8 hours) or PAN (0.10 microliter per liter for up to 8 hours). Ozone increased phospholipids in morning glory and decreased in kidney bean at the initial stage (2-4 hours) of exposure, while it scarcely changed glycolipids, the unsaturated fatty acids, and MDA in both plants. A large reduction of glycolipids occurred 1 day after ozone exposure in both plants. PAN caused marked drops in phospholipids and glycolipids in kidney bean at relatively late stage (6-8 hours) of exposure, while it increased phosphatidic acid and decreased the unsaturated fatty acids, an increase which was accompanied by a large increase in MDA. These results suggest that ozone may not directly oxidize unsaturated fatty acids at the initial stage of exposure, but may alter polar lipid metabolism, particularly phospholipids. On the other hand, PAN may abruptly and considerably degrade phospholipids and glycolipids by peroxidation or hydrolysis at the late stage of exposure. The present study shows that ozone and PAN affect polar lipids in different manners. Images Fig. 2 Fig. 3 PMID:16666199

  13. Pulmonary Responses in Healthy Young Adults Exposed to Low Concentration of Ozone for 6.6 Hours with Mild Exercise

    EPA Science Inventory

    Rational: Recent studies have shown small but significant decreases in lung function following a prolonged exposure (6.6 hour) of healthy young adults to levels of ozone (0.08 ppm) near the current 8 hour standard. It is unclear, however, if such effects may be extended to concen...

  14. Evaluation of microporous carbon filters as catalysts for ozone decomposition

    SciTech Connect

    Whinnery, L.; Coutts, D.; Shen, C.; Adams, R.; Quintana, C.; Showalter, S.

    1994-12-31

    Ozone is produced in small quantities in photocopiers and laser printers in the workplace and large quantities in industrial waste water treatment facilities. Carbon filters are commonly used to decompose this unwanted ozone. The three most important factors in producing a filter for this purpose are flow properties, efficiency, and cost. Most ozone decomposition applications require very low back-pressure at modest flow rates. The tradeoff between the number of pores and the size of the pores will be discussed. Typical unfiltered emissions in the workplace are approximately 1 ppm. The maximum permissible exposure limit, PEL, for worker exposure to ozone is 0.1 ppm over 8 hours. Several methods have been examined to increase the efficiency of ozone decomposition. Carbon surfaces were modified with catalysts, the surface activated, and the surface area was increased, in attempts to decompose ozone more effectively. Methods to reduce both the processing and raw material costs were investigated. Several sources of microporous carbon were investigated as ozone decomposition catalysts. Cheaper processing routes including macropore templating, faster drying and extracting methods were also studied.

  15. Evaluation of Global Model Simulation of Tropospheric Ozone from ECHAM6-HAMMOZ1 with Surface Measurements over the Mediterranean Region

    NASA Astrophysics Data System (ADS)

    Kaffashzadeh, Najmeh; Schultz, Martin G.; Lyapina, Olga; Schröder, Sabine; Stadtler, Scarlet

    2016-04-01

    Current chemistry transport models are generally successful in describing the principle features of the present-day global tropospheric ozone (O3) distribution, but they exhibit large differences of ozone concentrations over the Mediterranean region. The Mediterranean region can be perturbed by long-range pollution import from Northern Europe, North Africa and Asia, in addition to local emissions, which may all contribute to ozone concentrations in this area. Identifying the main drivers for Mediterranean ozone concentrations and understanding the reasons for the inter-model differences remain scientific challenges. To investigate the geographical distribution of tropospheric ozone over the Mediterranean, we analyze hourly surface ozone measurements from more than 1000 stations in the Tropospheric Ozone Assessment Report (TOAR) database and compare these to hourly model outputs from the global chemistry climate model ECHAM6-HAMMOZ1 for the year 2012. The daily maximum 8-hour running mean value of ozone mixing ratios is calculated for both model and observation and compared. The preliminary results show that the model captures many features of the ozone and its precursor concentrations in many regions of Europe throughout the year. However, it substantially underestimates ozone in the Po Valley region in summer and overestimates ozone over much of the Mediterranean region during spring. The reasons for this behavior will be investigated through detailed sensitivity studies with respect to VOC emissions, anthropogenic emissions, ozone deposition, specific chemical reactions, and long range-import of ozone and precursors.

  16. Observations of the Antarctic Ozone Hole from 2003 to 2014

    NASA Astrophysics Data System (ADS)

    Braathen, Geir O.

    2015-04-01

    The Global Atmosphere Watch of WMO includes several stations in Antarctica that keep a close eye on the ozone layer during the ozone hole season. Observations made during the ozone holes from 2003 to 2014 will be compared to each other and interpreted in light of the meteorological conditions. Satellite observations will be used to get a more general picture of the size and depth of the ozone hole and will also be used to calculate various metrics for ozone hole severity. In 2003, 2005 and 2006, the ozone hole was relatively large with more ozone loss than normal. This is in particular the case for 2006, which by most ozone hole metrics was the most severe ozone hole on record. On the other hand, the ozone holes of 2004, 2007, 2010 and 2012 were less severe than normal, and only the very special ozone hole of 2002 had less ozone depletion when one regards the ozone holes of the last decade. The ozone hole of 2011 suffered more ozone depletion than in 2010, but it was quite average in comparison to other years of the last decade. The situation was similar in 2013 and 2014. The interannual variability will be discussed with the help of meteorological data, such as temperature conditions, possibility for polar stratospheric clouds, vortex shape and vortex longevity.

  17. Observations of the Antarctic Ozone Hole from 2003 to 2013

    NASA Astrophysics Data System (ADS)

    Braathen, Geir O.

    2014-05-01

    The Global Atmosphere Watch of WMO includes several stations in Antarctica that keep a close eye on the ozone layer during the ozone hole season. Observations made during the ozone holes from 2003 to 2013 will be compared to each other and interpreted in light of the meteorological conditions. Satellite observations will be used to get a more general picture of the size and depth of the ozone hole and will also be used to calculate various metrics for ozone hole severity. In 2003, 2005 and 2006, the ozone hole was relatively large with more ozone loss than normal. This is in particular the case for 2006, which by most ozone hole metrics was the most severe ozone hole on record. On the other hand, the ozone holes of 2004, 2007, 2010 and 2012 were less severe than normal, and only the very special ozone hole of 2002 had less ozone depletion when one regards the ozone holes of the last decade. The ozone hole of 2011 suffered more ozone depletion than in 2010, but it was quite average in comparison to other years of the last decade. The situation was similar in 2013. The interannual variability will be discussed with the help of meteorological data, such as temperature conditions, possibility for polar stratospheric clouds, vortex shape and vortex longevity. Observations will also be compared to 3-D chemical transport model calculations.

  18. Evaluation of emission control strategies to reduce ozone pollution in the Paso del Norte region using a photochemical air quality modeling system

    NASA Astrophysics Data System (ADS)

    Valenzuela, Victor Hugo

    Air pollution emissions control strategies to reduce ozone precursor pollutants are analyzed by applying a photochemical modeling system. Simulations of air quality conditions during an ozone episode which occurred in June, 2006 are undertaken by increasing or reducing area source emissions in Ciudad Juarez, Chihuahua, Mexico. Two air pollutants are primary drivers in the formation of tropospheric ozone. Oxides of nitrogen (NOx) and volatile organic compounds (VOC) undergo multiple chemical reactions under favorable meteorological conditions to form ozone, which is a secondary pollutant that irritates respiratory systems in sensitive individuals especially the elderly and young children. The U.S. Environmental Protection Agency established National Ambient Air Quality Standards (NAAQS) to limit ambient air pollutants such as ozone by establishing an 8-hour average concentration of 0.075 ppm as the threshold at which a violation of the standard occurs. Ozone forms primarily due reactions in the troposphere of NOx and VOC emissions generated primarily by anthropogenic sources in urban regions. Data from emissions inventories indicate area sources account for ˜15 of NOx and ˜45% of regional VOC emissions. Area sources include gasoline stations, automotive paint bodyshops and nonroad mobile sources. Multiplicity of air pollution emissions sources provides an opportunity to investigate and potentially implement air quality improvement strategies to reduce emissions which contribute to elevated ozone concentrations. A baseline modeling scenario was established using the CAMx photochemical air quality model from which a series of sensitivity analyses for evaluating air quality control strategies were conducted. Modifications to area source emissions were made by varying NOx and / or VOC emissions in the areas of particular interest. Model performance was assessed for each sensitivity analysis. Normalized bias (NB) and normalized error (NE) were used to identify

  19. Quantitative characterization of the Antarctic ozone hole

    NASA Technical Reports Server (NTRS)

    Ito, T.; Sakoda, Y.; Matsubara, K.; Takao, T.; Akagi, K.; Watanabe, Y.; Shibata, S.; Naganuma, H.

    1994-01-01

    The long-term evolution of the Antarctic ozone hole is studied based on the TOMS data and the JMA data-set of stratospheric temperature in relation with the possible role of polar stratospheric clouds (PSC's). The effective mass of depleted ozone in the ozone hole at its annual mature stage reached a historical maximum of 55 Mt in 1991, 4.3 times larger than in 1981. The ozone depletion rate during 30 days before the mature ozone hole does not show any appreciable long-term trend but the interannual fluctuations do, ranging from 0.169 to 0.689 Mt/day with the average of 0.419 Mt/day for the period of 1979 - 1991. The depleted ozone mass has the highest correlation with the region below 195 K on the 30 mb surface in June, whereas the ozone depletion rate correlates most strongly with that in August. The present result strongly suggests that the long-term evolution of the mature ozone hole is caused both by the interannual change of the latitudinal coverage of the early PSC's, which may control the latitude and date of initiation of ozone decrease, and by that of the spatial coverage of the mature PSC's which may control the ozone depletion rate in the Antarctic spring.

  20. Effects of stratospheric ozone recovery on tropospheric chemistry and air quality

    NASA Astrophysics Data System (ADS)

    Zhang, H.; Wu, S.; Wang, Y.

    2013-08-01

    The stratospheric ozone has decreased greatly since 1980 due to ozone depleting substances (ODSs). As a result of the implementation of the Montreal Protocol and its amendments and adjustments, stratospheric ozone is expected to recover towards its pre-1980 level in the coming decades. We examine the implications of stratospheric ozone recovery for the tropospheric chemistry and ozone air quality with a global chemical transport model (GEOS-Chem). Significant decreases in surface ozone photolysis rates due to stratospheric ozone recovery are simulated. Increases in ozone lifetime by up to 7% are calculated in the troposphere. The global average OH decreases by 1.74% and the global burden of tropospheric ozone increases by 0.78%. The perturbations to tropospheirc ozone and surface ozone show large seasonal and spatial variations. General increases in surface ozone are calculated for each season, with increases by up to 5% for some regions.

  1. Impacts of Stratospheric Ozone Change on Tropospheric Chemistry and Air Quality

    NASA Astrophysics Data System (ADS)

    Wu, S.; Zhang, H.

    2013-05-01

    The stratospheric ozone has decreased greatly since 1980 due to ozone depleting substances (ODSs). As a result of the implementation of the Montreal Protocol and its Amendments and Adjustments, stratospheric ozone is expected to recover towards its pre-1980 level in the coming decades. We examine the implications of stratospheric ozone recovery for the tropospheric chemistry and ozone air quality with a global chemical transport model (GEOS-Chem). Significant decreases in surface ozone photolysis rates due to stratospheric ozone recovery are simulated. Increases in ozone lifetime by up to 7% are calculated in the troposphere. The global average OH decreases by 1.74% and the global burden of tropospheric ozone increased by 0.78%. The perturbations to tropospheirc ozone and surface ozone show large seasonal and spatial variations. General increases in surface ozone are calculated for each season, with increases by up to 5% for some regions.

  2. Ozone uptake by citrus trees exposed to a range of ozone concentrations

    NASA Astrophysics Data System (ADS)

    Fares, Silvano; Park, Jeong-Hoo; Ormeno, Elena; Gentner, Drew R.; McKay, Megan; Loreto, Francesco; Karlik, John; Goldstein, Allen H.

    2010-09-01

    The Citrus genus includes a large number of species and varieties widely cultivated in the Central Valley of California and in many other countries having similar Mediterranean climates. In the summer, orchards in California experience high levels of tropospheric ozone, formed by reactions of volatile organic compounds (VOC) with oxides of nitrogen (NO x). Citrus trees may improve air quality in the orchard environment by taking up ozone through stomatal and non-stomatal mechanisms, but they may ultimately be detrimental to regional air quality by emitting biogenic VOC (BVOC) that oxidize to form ozone and secondary organic aerosol downwind of the site of emission. BVOC also play a key role in removing ozone through gas-phase chemical reactions in the intercellular spaces of the leaves and in ambient air outside the plants. Ozone is known to oxidize leaf tissues after entering stomata, resulting in decreased carbon assimilation and crop yield. To characterize ozone deposition and BVOC emissions for lemon ( Citrus limon), mandarin ( Citrus reticulata), and orange ( Citrus sinensis), we designed branch enclosures that allowed direct measurement of fluxes under different physiological conditions in a controlled greenhouse environment. Average ozone uptake was up to 11 nmol s -1 m -2 of leaf. At low concentrations of ozone (40 ppb), measured ozone deposition was higher than expected ozone deposition modeled on the basis of stomatal aperture and ozone concentration. Our results were in better agreement with modeled values when we included non-stomatal ozone loss by reaction with gas-phase BVOC emitted from the citrus plants. At high ozone concentrations (160 ppb), the measured ozone deposition was lower than modeled, and we speculate that this indicates ozone accumulation in the leaf mesophyll.

  3. The Antarctic Ozone Hole

    ERIC Educational Resources Information Center

    Jones, Anna E.

    2008-01-01

    Since the mid 1970s, the ozone layer over Antarctica has experienced massive destruction during every spring. In this article, we will consider the atmosphere, and what ozone and the ozone layer actually are. We explore the chemistry responsible for the ozone destruction, and learn about why conditions favour ozone destruction over Antarctica. For…

  4. Total ozone measurements made with the Brewer ozone spectrophotometer during STOIC 1989

    NASA Astrophysics Data System (ADS)

    Kerr, J. B.; McElroy, C. T.

    1995-05-01

    The Canadian Atmospheric Environment Service participated in the Stratospheric Ozone Intercomparison Campaign (STOIC) by operating a Brewer ozone spectrophotometer at the Table Mountain Observatory from July 19 to August 2, 1989. Frequent direct Sun measurements of total column ozone were made throughout most days during the 2 weeks of the intercomparison. Results of the Brewer instrument total ozone measurements are given. They show that there is a diurnal variation of total ozone with values increasing on average by 6.6±2.4 Dobson units between early morning and late afternoon. Comparing the total ozone measurements with ozone concentration measurements made at ground level suggests that the daytime increase is a result of a buildup of surface ozone during the day. The total ozone measurements made by the Brewer instrument during STOIC are compared with total ozone measurements made by the National Oceanic and Atmospheric Administration (NOAA) Dobson instrument, the NASA/Wallops electrochemical concentration cell ozonesondes and the total ozone mapping spectrometer satellite instrument.

  5. Contribution of ozone to airborne aldehyde formation in Paris homes.

    PubMed

    Rancière, Fanny; Dassonville, Claire; Roda, Célina; Laurent, Anne-Marie; Le Moullec, Yvon; Momas, Isabelle

    2011-09-15

    Indoor aldehydes may result from ozone-initiated chemistry, mainly documented by experimental studies. As part of an environmental investigation included in the PARIS birth cohort, the aim of this study was to examine ozone contribution to airborne aldehyde formation in Paris homes. Formaldehyde, acetaldehyde and hexaldehyde levels, as well as styrene, nitrogen dioxide and nicotine concentrations, comfort parameters and carbon dioxide levels, were measured twice during the first year of life of the babies. Ambient ozone concentrations were collected from the closest background station of the regional air monitoring network. Traffic-related nitrogen oxide concentrations in front of the dwellings were estimated by an air pollution dispersion model. Home characteristics and families' way of life were described by questionnaires. Stepwise multiple linear regression models were used to link aldehyde levels with ambient ozone concentrations and a few aldehyde precursors involved in oxidation reactions, adjusting for other indoor aldehyde sources, comfort parameters and traffic-related nitrogen oxides. A 4 and 11% increase in formaldehyde and hexaldehyde levels was pointed out when 8-hour ozone concentrations increased by 20 μg/m(3). The influence of potential precursors such as indoor styrene level and frequent use of air fresheners, containing unsaturated volatile organic compounds as terpenes, was also found. Thus, our results suggest that ambient ozone can significantly impact indoor air quality, especially with regard to formaldehyde and hexaldehyde levels.

  6. Earth's Endangered Ozone

    ERIC Educational Resources Information Center

    Panofsky, Hans A.

    1978-01-01

    Included are (1) a discussion of ozone chemistry; (2) the effects of nitrogen fertilizers, fluorocarbons, and high level aircraft on the ozone layer; and (3) the possible results of a decreasing ozone layer. (MR)

  7. Ozone crisis

    SciTech Connect

    Roan, S.

    1989-01-01

    The author presents an account of the depletion of the atmosphere's ozone layer since the discovery of the phenomenon 15 years ago. The book recounts the flight to ban chlorofluorocarbons (CFC's) and describes the science, the people, and the politics involved, up to the March 1988 international treaty restricting CFC production. It surveys the media's coverage, describes the struggle for remedies, and offers a prognosis for the future.

  8. Response of macaque bronchiolar epithelium to ambient concentrations of ozone

    SciTech Connect

    Harkema, J.R.; Plopper, C.G.; Hyde, D.M.; St. George, J.A.; Wilson, D.W.; Dungworth, D.L. )

    1993-09-01

    Recently, we reported that exposure to ambient concentrations of ozone, near the U.S. National Ambient Air Quality Standard (0.12 ppm), induced significant nasal epithelial lesions in a non-human primate, the bonnet monkey. The present study defines the effects of ambient concentrations of ozone on the surface epithelium lining respiratory bronchioles and on the underlying bronchiolar interstitium in these same monkeys. Bonnet monkeys were exposed to filtered air or to 0.15 or 0.30 ppm ozone 8 hours/day for 6 or 90 days. At the end of exposures, monkeys were anesthetized and killed by exsanguination. Microdissected bronchiolar airways of infusion-fixed lungs were evaluated morphometrically by light microscopy and quantitatively by scanning and transmission electron microscopy for ozone-induced epithelial changes. Hyperplasia of nonciliated, cuboidal epithelial cells and intraluminal accumulation of macrophages characterized ozone-induced lesions in respiratory bronchioles. There were no significant differences in epithelial thickness or cell numbers among ozone-exposed groups. Ozone-exposed epithelium was composed of 80% cuboidal and 20% squamous cells compared with 40% cuboidal and 60% squamous cells in filtered air controls. In addition, the arithmetic mean thickness of the surface epithelium, a measure of tissue mass per unit area of basal lamina, was significantly increased in all of the ozone-exposed groups. The number of cuboidal epithelial cells per surface area of basal lamina was increased above control values by 780% after 6 days exposure to 0.15 ppm, 777% after 90 days to 0.15 ppm, and 996% after 90 days exposure to 0.30 ppm. There was also a significant ozone-induced increase in the thickness of the bronchiolar interstitium that was due to an increase in both cellular and acellular components.

  9. Mesospheric ozone measurements by SAGE II

    NASA Astrophysics Data System (ADS)

    Chu, D. A.; Cunnold, D. M.

    1994-04-01

    SAGE II observations of ozone at sunrise and sunset (solar zenith angle = 90 deg) at approximately the same tropical latitude and on the same day exhibit larger concentrations at sunrise than at sunset between 55 and 65 km. Because of the rapid conversion between atomic oxygen and ozone, the onion-peeling scheme used in SAGE II retrievals, which is based on an assumption of constant ozone, is invalid. A one-dimensional photochemical model is used to simulate the diurnal variation of ozone particularly within the solar zenith angle of 80 deg - 100 deg. This model indicates that the retrieved SAGE II sunrise and sunset ozone values are both overestimated. The Chapman reactions produce an adequate simulation of the ozone sunrise/sunset ratio only below 60 km, while above 60 km this ratio is highly affected by the odd oxygen loss due to odd hydrogen reactions, particularly OH. The SAGE II ozone measurements are in excellent agreement with model results to which an onion peeling procedure is applied. The SAGE II ozone observations provide information on the mesospheric chemistry not only through the ozone profile averages but also from the sunrise/sunset ratio.

  10. Mesospheric ozone measurements by SAGE II

    NASA Technical Reports Server (NTRS)

    Chu, D. A.; Cunnold, D. M.

    1994-01-01

    SAGE II observations of ozone at sunrise and sunset (solar zenith angle = 90 deg) at approximately the same tropical latitude and on the same day exhibit larger concentrations at sunrise than at sunset between 55 and 65 km. Because of the rapid conversion between atomic oxygen and ozone, the onion-peeling scheme used in SAGE II retrievals, which is based on an assumption of constant ozone, is invalid. A one-dimensional photochemical model is used to simulate the diurnal variation of ozone particularly within the solar zenith angle of 80 deg - 100 deg. This model indicates that the retrieved SAGE II sunrise and sunset ozone values are both overestimated. The Chapman reactions produce an adequate simulation of the ozone sunrise/sunset ratio only below 60 km, while above 60 km this ratio is highly affected by the odd oxygen loss due to odd hydrogen reactions, particularly OH. The SAGE II ozone measurements are in excellent agreement with model results to which an onion peeling procedure is applied. The SAGE II ozone observations provide information on the mesospheric chemistry not only through the ozone profile averages but also from the sunrise/sunset ratio.

  11. User's guide for SBUV/TOMS ozone derivative products

    NASA Technical Reports Server (NTRS)

    Fleig, A. J.; Wellemeyer, C.; Oslik, N.; Lee, D.; Miller, J.; Magatani, R.

    1984-01-01

    A series of products are available derived from the total-ozone and ozone vertical profile results for the Solar Backscattered Ultraviolet/Total-Ozone Mapping Spectrometer (SBUV/TOMS) Nimbus-7 operation. Products available are (1) orbital height-latitude cross sections of the SBUV profile data, (2) daily global total ozone contours in polar coordinates, (3) daily averages of total ozone in global 5x5 degree latitude-longitude grid, (4) daily, monthly and quarterly averages of total ozone and profile data in 10 degree latitude zones, (5) tabular presentation of zonal means, (6) daily global total ozone and profile contours in polar coordinates. The ""Derivative Products User's Guide'' describes each of these products in detail, including their derivation and presentation format. Information is provided on how to order the tapes and microfilm from the National Space Science Data Center.

  12. Effect of photoperiodic pretreatments on symptom development in plants exposed to ozone

    SciTech Connect

    Godish, T.

    1980-01-01

    Results presented in this report on the effects of photoperiodic pretreatment on ozone sensitivity of plants are significantly different from the lone previous report on this subject. Juhren et al (5) studied the effects of photoperiodic pretreatments on sensitivity of pinto beans exposed to oxidants (presumably ozone). They reported that pinto bean plants were most sensitive to oxidants under short photoperiods (8 hours) and least sensitive to long photoperiods (16 hours). In studies of tomato and peas presented in this report, minimum sensitivity for tomato was observed under the 8 hour pretreatment; for peas minimum sensitivity was observed for the 8 and 10 hour pretreatments. Maximum sensitivity for tomato was observed for the 12-hour photoperiodic pretreatment; peas showed maximum sensitivity under the 14-hour photoperiod. 7 references, 1 table.

  13. Effects of ozone and peroxyacetyl nitrate on polar lipids and fatty acids in leaves of morning glory and kidney bean. [Pharbitis nil; Phaseolus vulgaris

    SciTech Connect

    Nouchi, Isamu; Toyama, Susumu Ochanomizu Univ., Tokyo )

    1988-07-01

    To compare the effects of ozone and peroxyacetyl nitrate (PAN) on leaf lipids, fatty acids and malondialdehyde (MDA), morning glory (Pharbitis nil Choisy cv Scarlet O'Hara) and kidney bean (Phaseolus vulgaris L. cv Gintebo) plants were exposed to either ozone (0.15 microliter per liter for 8 hours) or PAN (0.10 microliter per liter for up to 8 hours). Ozone increased phospholipids in morning glory and decreased in kidney bean at the initial stage (2-4 hours) of exposure, while it scarcely changed glycolipids, the unsaturated fatty acids, and MDA in both plants. A large reduction of glycolipids occurred 1 day after ozone exposure in both plants. PAN caused marked drops in phospholipids and glycolipids in kidney bean at relatively late stage (6-8 hours) of exposure, while it increased phosphatidic acid and decreased the unsaturated fatty acids, an increase which was accompanied by a large increase in MDA. These results suggest that ozone may not directly oxidize unsaturated fatty acids at the initial stage of exposure, but may alter polar lipid metabolism, particularly phospholipids. On the other hand, PAN may abruptly and considerably degrade phospholipids and glycolipids by peroxidation or hydrolysis at the late stage of exposure. The present study shows that ozone and PAN affect polar lipids in different manners.

  14. [Temporal and spatial distribution characteristics of ozone in Beijing].

    PubMed

    Wang, Zhan-shan; Li, Yun-ting; Chen, Tian; Zhang, Da-wei; Sun, Feng; Sun, Rui-wen; Dong, Xin; Sun, Nai-di; Pan, Li-bo

    2014-12-01

    Ozone concentrations obtained from 35 automatic air monitoring stations in Beijing were analyzed to investigate their temporal and spatial distribution characteristics. A process with high ozone concentration in summer was analyzed. The results showed that ozone maintained relatively high concentration from May to August while in other months, the ozone concentration was at a low level. Overall, the average concentrations of ozone in different stations in a descending order were comparison and regional station, suburban environment evaluation station, urban environmental assessment station and traffic pollution monitoring station. Ozone diurnal variation showed a single peak distribution, the peak of which appeared at 15:00 or 16:00. Ozone concentration showed obvious weekend effect, which meant ozone concentration in daytime of weekend was higher than that in weekday. Ozone concentration was lower in urban Beijing, higher in surrounding counties and the highest in northeast area with more vegetation. A high ozone concentration process occurred in Beijing on June 3, 2013. Under the effect of southwest wind in the afternoon, the concentration peaks of ozone in Yufa, Fengtaihuayuan, Olympic center and Huairou station occurred in order from south to north. Concentration peak of ozone in Huairou station occurred at 20:00 in the night. It could be concluded that significant ozone transmission characteristic was reflected in this process.

  15. [Characteristics of acid red 3R wastewater treatment by ozone microbubbles].

    PubMed

    Zhang, Jing; Du, Ya-Wei; Liu, Xiao-Jing; Zhou, Yu-Wen; Liu, Chun; Yang, Jing-Liang; Zhang, Lei

    2015-02-01

    The application of microbubble technology for ozonation wastewater treatment could enhance ozone mass transfer, improve ozonation performance and increase ozone utilization efficiency. The ozone microbubbles were used to treat synthetic acid red 3R wastewater in the present study, and compared to ozone conventional bubbles. The ozone mass transfer and ozonation characteristics of acid red 3R were investigated when ozone microbubbles and ozone conventional bubbles were applied. The results confirmed the enhanced ozone mass transfer using microbubbles. The ozone mass transfer coefficient using microbubbles was 3.6 times higher than that using conventional bubbles under the same conditions. Simultaneously, the ozone decomposition coefficient using microbubbles was 6.2 times higher than that using conventional bubbles, which would be favorable for *OH generation. The ozonation rate and mineralization efficiency of acid red 3R could be improved significantly using ozone microbubbles. A TOC removal efficiency of 78.0% was achieved using ozone microbubbles, which was about 2 times higher than that using ozone conventional bubbles. The ozone utilization efficiency using microbubbles was much higher that using conventional bubbles during ozonation treatment of acid red 3R. The average ozone utilization efficiencies were 97.8% and 69.3% when microbubbles and conventional bubbles were used, respectively. The oxidative ability of ozone microbubbles could be increased by enhancing *OH generation, and as a result, the oxidative reaction of degradation intermediates was accelerated by ozone microbubbles. Especially, the mineralization ability of small organic acid intermediates using ozone microbubbles was about 1.6 times higher than that using ozone conventional bubbles.

  16. Effects of nitrogen oxide emission controls on Eastern US surface ozone: A comparison between urban cores and rural background sites

    NASA Astrophysics Data System (ADS)

    Rieder, Harald E.; Fiore, Arlene M.

    2016-04-01

    Nitrogen oxide (NOx) emission controls have led to improved air quality over the past two decades, particularly over the Eastern US. In recent work we quantified the effects of the efforts to abate surface ozone (O3) pollution under the NOx State Implementation Plan (NOx SIP Call) for Eastern US background sites (available from the Clean Air Status and Trends Network (CASTNET)) using methods from statistical extreme value theory (Rieder et al., 2013). Our analysis showed that the number of summer (JJA) days above the US national ambient air quality standard (NAAQS) declined on average by a factor of two between 1988-1998 and 1999-2009 and that probabilistic 1-yr O3 return values declined by about 10 ppb between these two time periods. Here we extend the analysis to observations available from the US EPA Air Quality System (AQS), comprising sites ranging from polluted urban cores to rural sites. We focus on changes in (i) the seasonal and annual average number of days with maximum daily 8-hour average surface O3 above the NAAQS and (ii) probabilistic O3 return values following the NOx SIP Call. Particular focus is given on similarities and differences in surface O3 responses on regional to local level and on contrasting urban cores and rural background sites. References: Rieder H.E., Fiore A.M., Polvani L.M., Lamarque J.-F., Fang Y. (2013): Changes in the frequency and return level of high ozone pollution events over the Eastern United States following emission controls, Environ. Res. Lett., 8, 014012, 2013.

  17. Record low global ozone in 1992

    NASA Astrophysics Data System (ADS)

    Gleason, J. F.; Bhartia, P. K.; Herman, J. R.; McPeters, R.; Newman, P.; Stolarski, R. S.; Flynn, L.; Labow, G.; Larko, D.; Seftor, C.

    1993-04-01

    The 1992 global average total ozone, measured by the Total Ozone Mapping Spectrometer (TOMS) on the Nimbus-7 satellite, was 2 to 3 percent lower than any earlier year observed by TOMS (1979 to 1991). Ozone amounts were low in a wide range of latitudes in both the Northern and Southern Hemispheres, and the largest decreases were in the regions from 10 to 20 deg S and 10 to 60 deg N. Global ozone in 1992 is at least 1.5 percent lower than would be predicted by a statistical model that includes a linear trend and accounts for solar cycle variation and the quasi-biennial oscillation. These results are confirmed by comparisons with data from other ozone monitoring instruments: the SBUV/2 instrument on the NOAA-11 satellite, the TOMS instrument on the Russian Meteor-3 satellite, the World Standard Dobson Instrument 83, and a collection of 22 ground-based Dobson instruments.

  18. Influence of the ozone profile above Madrid (Spain) on Brewer estimation of ozone air mass factor

    NASA Astrophysics Data System (ADS)

    Antón, M.; López, M.; Costa, M. J.; Serrano, A.; Bortoli, D.; Bañón, M.; Vilaplana, J. M.; Silva, A. M.

    2009-08-01

    The methodology used by Brewer spectroradiometers to estimate the ozone column is based on differential absorption spectroscopy. This methodology employs the ozone air mass factor (AMF) to derive the total ozone column from the slant path ozone amount. For the calculating the ozone AMF, the Brewer algorithm assumes that the ozone layer is located at a fixed height of 22 km. However, for a real specific site the ozone presents a certain profile, which varies spatially and temporally depending on the latitude, altitude and dynamical conditions of the atmosphere above the site of measurements. In this sense, this work address the reliability of the mentioned assumption and analyses the influence of the ozone profiles measured above Madrid (Spain) in the ozone AMF calculations. The approximated ozone AMF used by the Brewer algorithm is compared with simulations obtained using the libRadtran radiative transfer model code. The results show an excellent agreement between the simulated and the approximated AMF values for solar zenith angle lower than 75°. In addition, the relative differences remain lower than 2% at 85°. These good results are mainly due to the fact that the altitude of the ozone layer assumed constant by the Brewer algorithm for all latitudes notably can be considered representative of the real profile of ozone above Madrid (average value of 21.7±1.8 km). The operational ozone AMF calculations for Brewer instruments are limited, in general, to SZA below 80°. Extending the usable SZA range is especially relevant for Brewer instruments located at high mid-latitudes.

  19. Decadal evolution of the Antarctic ozone hole

    NASA Technical Reports Server (NTRS)

    Jiang, Y.; Yung, Y. L.; Zurek, R. W.

    1996-01-01

    Ozone column amounts obtained by the total ozone mapping spectrometer (TOMS) in the southern polar region are analyzed during late austral winter and spring (days 240-300) for 1980-1991 using area-mapping techniques and area-weighted vortex averages. The vortex here is defined using the -50 PVU (1 PVU = 1.0 x 10(-6) K kg-1 m2 s-1) contour on the 500 K isentropic surface. The principal results are: (1) there is a distinct change after 1985 in the vortex-averaged column ozone depletion rate during September and October, the period of maximum ozone loss, and (2) the vortex-averaged column ozone in late August (day 240) has dropped by 70 Dobson units (DU) in a decade due to the loss in the dark and the dilution effect. The mean ozone depletion rate in the vortex between day 240 and the day of minimum vortex-averaged ozone is about 1 DU d-1 at the beginning of the decade, increasing to about 1.8 DU d-1 by 1985, and then apparently saturating thereafter. The vortex-average column ozone during September and October has declined at the rate of 11.3 DU yr-1 (3.8%) from 1980 to 1987 (90 DU over 8 years) and at a smaller rate of 2 DU yr-1 (0.9%) from 1987 to 1991 (10 DU over 5 years, excluding the anomalous year 1988). We interpret the year-to-year trend in the ozone depletion rate during the earlier part of the decade as due to the rise of anthropogenic chlorine in the atmosphere. The slower trend at the end of the decade indicates saturation of ozone depletion in the vortex interior, in that chlorine amounts in the mid-1980s were already sufficiently high to deplete most of the ozone in air within the isolated regions of the lower-stratospheric polar vortex. In subsequent years, increases in stratospheric chlorine may have enhanced wintertime chemical loss of ozone in the south polar vortex even before major losses during the Antarctic spring.

  20. Comparative Effects of Gamma Irradiation and Ozone Treatment on Hygienic Quality of Korean Red Ginseng Powder

    NASA Astrophysics Data System (ADS)

    Byun, Myung-Woo; Yook, Hong-Sun; Kang, Il-Jun; Chung, Cha-Kwon; Kwon, Joong-Ho; Choi, Kang-Ju

    1998-06-01

    For the purpose of improving hygienic quality of Korean red ginseng powder, the comparative effects of gamma irradiation and ozone treatment on the microbial and physicochemical properties were investigated. Gamma irradiation at 7.5 kGy resulted in sterilization of total aerobic bacteria, molds and coliforms below detective levels, while ozone treatment for 8 hours up to 18 ppm did not sufficiently eliminate the microorganisms of the red ginseng powder. Physicochemical properties including compositions of the red ginseng saponin (ginsenosides) and fatty acids, pH and hydrogen doanting activity were not significantly changed by gamma irradiation, whereas, ozone treatment caused significant changes in fatty acid compositions, TBA value, pH, acidity and hydrogen donating activity. The results from this study led us to conclude that gamma irradiation was more effective than ozone treatment both for the improvement of hygienic quality and for the maintenance of physicochemical quality of red ginseng powder.

  1. Ozone Hole Over Antarctica

    NASA Technical Reports Server (NTRS)

    2002-01-01

    These images from the Total Ozone Mapping Spectrometer (TOMS) show the progressive depletion of ozone over Antarctica from 1979 to 1999. This 'ozone hole' has extended to cover an area as large as 10.5 million square miles in September 1998. The previous record of 10.0 million square miles was set in 1996. The Antarctic ozone hole develops each year between late August and early October. Regions with higher levels of ozone are shown in red. NASA and NOAA instruments have been measuring Antarctic ozone levels since the early 1970s. Large regions of depleted ozone began to develop over Antarctica in the early 1980s. Ozone holes of substantial size and depth are likely to continue to form during the next few years, scientists hope to see a reduction in ozone loss as levels of ozone-destroying CFCs (chlorofluorocarbons) are gradually reduced. Credit: Images by Greg Shirah, NASA Goddard Space Flight Center Scientific Visualization Studio

  2. Ozone profiles above Palmer Station, Antarctica

    NASA Technical Reports Server (NTRS)

    Torres, Arnold L.; Brothers, George

    1988-01-01

    NASA's Goddard Space Flight Center/Wallops Flight Facility conducted a series of 52 balloon-borne measurements of vertical ozone profiles over the National Science Foundation (NSF) research facility at Palmer Station, Antarctica (64 deg 46 S, 64 deg 3 W) between August 9 and October 24, 1987. High resolution measurements were made from ground level to an average of 10 mb. While much variation was seen in the profile amounts of ozone, it is clear that a progressive depletion of ozone occurred during the measurement period, with maximum depletion taking place in the 17 to 19 km altitude region. Ozone partial pressures dropped by about 95 percent in this region. Shown here are plotted time dependences of ozone amounts observed at 17 km and at arbitrarily selected altitudes below (13 km) and above (24 km) the region of maximum depletion. Ozone partial pressure at 17 km is about 150nb in early August, and has decreased to less than 10nb in the minimums in October. The loss rate is of the order of 1.5 percent/day. In summary, a progressive depletion in stratospheric ozone over Palmer Station was observed from August to October, 1987. Maximum depletion occurred in the 17 to 19 km range, and amounted to 95 percent. Total ozone overburden decreased by up to 50 percent during the same period.

  3. Recovery of the Antarctic Ozone Hole

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.; Nash, Eric R.; Kawa, S. Randolph; Montzka, Steve; Schauffler, Sue; Stolarski, Richard S.; Douglass, Anne R.; Pawson, Steven; Nielsen, J. Eric

    2006-01-01

    The Antarctic ozone hole develops each year and culminates by early Spring. Antarctic ozone values have been monitored since 1979 using satellite observations from the TOMS and OMI instruments. The severity of the hole has been assessed using the minimum total ozone value from the October monthly mean (depth of the hole), the average size during the September-October period, and the ozone mass deficit. Ozone is mainly destroyed by halogen catalytic cycles, and these losses are modulated by temperature variations in the collar of the polar lower stratospheric vortex. In this presentation, we show the relationships of halogens and temperature to both the size and depth of the hole. Because atmospheric halogen levels are responding to international agreements that limit or phase out production, the amount of halogens in the stratosphere should decrease over the next few decades. We use two methods to estimate ozone hole recovery. First, we use projections of halogen levels combined with age-of-air estimates in a parametric model. Second, we use a coupled chemistry climate model to assess recovery. We find that the ozone hole is recovering at an extremely slow rate and that large ozone holes will regularly recur over the next 2 decades. Furthermore, full recovery to 1980 levels will not occur until approximately 2068. We will also show some error estimates of these dates and the impact of climate change on the recovery.

  4. When Will the Antarctic Ozone Hole Recover?

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.

    2006-01-01

    The Antarctic ozone hole develops each year and culminates by early spring (late September - early October). Antarctic ozone values have been monitored since 1979 using satellite observations from the TOMS instrument. The severity of the hole has been assessed from TOMS using the minimum total ozone value from the October monthly mean (depth of the hole) and by calculating the average area coverage during this September-October period. Ozone is mainly destroyed by halogen (chlorine and bromine) catalytic cycles, and these losses are modulated by temperature variations in the collar of the polar lower stratospheric vortex. In this talk, I will show the relationships of halogens and temperature to both the size and depth of the hole. Because atmospheric halogen levels are responding to international agreements that limit or phase out production, the amount of halogens in the stratosphere should decrease over the next few decades. Using projections of halogen levels combined with age-of-air estimates, we find that the ozone hole is recovering at an extremely slow rate and that large ozone holes will regularly recur over the next 2 decades. The ozone hole will begin to show first signs of recovery in about 2023, and the hole will fully recover to pre-1980 levels in approximately 2070. This 2070 recovery is 20 years later than recent projections. I will also discuss current assessments of mid-latitude ozone recovery.

  5. The Antarctic ozone hole

    NASA Technical Reports Server (NTRS)

    Molina, Mario J.

    1988-01-01

    Observations of Antarctic ozone levels and the discovery of a hole in the Antarctic region are examined. The effects of chlorofluorocarbons (CFCs) on the level of stratospheric ozone are analyzed. Three cycles explaining the cause of ozone depletion in the poles are proposed. A comparison of field data and proposed depletion cycles reveals that the chemical origin of the ozone hole is due to CFCs. The potential global effects of the Antarctic ozone hole are discussed.

  6. Spatial distribution of tropospheric ozone in western Washington, USA

    USGS Publications Warehouse

    Cooper, S.M.; Peterson, D.L.

    2000-01-01

    We quantified the distribution of tropospheric ozone in topographically complex western Washington state, USA (total area a??6000 km2), using passive ozone samplers along nine river drainages to measure ozone exposure from near sea level to high-elevation mountain sites. Weekly average ozone concentrations were higher with increasing distance from the urban core and at higher elevations, increasing a mean of 1.3 ppbv per 100 m elevation gain for all mountain transects. Weekly average ozone concentrations were generally highest in Cascade Mountains drainages east and southeast of Seattle (maximum=55a??67 pbv) and in the Columbia River Gorge east of Portland (maximum=59 ppbv), and lowest in the western Olympic Peninsula (maximum=34 ppbv). Higher ozone concentrations in the Cascade Mountains and Columbia River locations downwind of large cities indicate that significant quantities of ozone and ozone precursors are being transported eastward toward rural wildland areas by prevailing westerly winds. In addition, temporal (week to week) variation in ozone distribution is synchronous within and between all drainages sampled, which indicates that there is regional coherence in air pollution detectable with weekly averages. These data provide insight on large-scale spatial variation of ozone distribution in western Washington, and will help regulatory agencies optimize future monitoring networks and identify locations where human health and natural resources could be at risk.

  7. Spatial distribution of tropospheric ozone in western Washington, USA.

    PubMed

    Cooper, S M; Peterson, D L

    2000-03-01

    We quantified the distribution of tropospheric ozone in topographically complex western Washington state, USA (total area approximately 6000 km(2)), using passive ozone samplers along nine river drainages to measure ozone exposure from near sea level to high-elevation mountain sites. Weekly average ozone concentrations were higher with increasing distance from the urban core and at higher elevations, increasing a mean of 1.3 ppbv per 100 m elevation gain for all mountain transects. Weekly average ozone concentrations were generally highest in Cascade Mountains drainages east and southeast of Seattle (maximum=55-67 pbv) and in the Columbia River Gorge east of Portland (maximum=59 ppbv), and lowest in the western Olympic Peninsula (maximum=34 ppbv). Higher ozone concentrations in the Cascade Mountains and Columbia River locations downwind of large cities indicate that significant quantities of ozone and ozone precursors are being transported eastward toward rural wildland areas by prevailing westerly winds. In addition, temporal (week to week) variation in ozone distribution is synchronous within and between all drainages sampled, which indicates that there is regional coherence in air pollution detectable with weekly averages. These data provide insight on large-scale spatial variation of ozone distribution in western Washington, and will help regulatory agencies optimize future monitoring networks and identify locations where human health and natural resources could be at risk. PMID:15092980

  8. Ozone depletion at northern and southern latitudes derived from January 1979 to December 1991 Total Ozone Mapping Spectrometer Data

    SciTech Connect

    Herman, J.R.; McPeters, R.; Larko, D.

    1993-07-20

    Long-term ozone depletion rates (percentage change) have been computed from 13 years of Nimbus 8/Total Ozone Mapping Spectrometer (TOMS) data as a function of latitude, longitude, and month for the period January 1, 1979, to December 31, 1991. In both hemispheres the amount of ozone has decreased at latitudes above 30{degrees} by amounts that are larger than predicted by homogeneous chemistry models for the 13-year time period. The largest rates of ozone decrease occur in the southern hemisphere during winter and spring, with partial recovery during the summer and autumn. Outside of the Antarctic ozone hole region, the 12-year ozone depletion rates reach 8-10% per decade during the winter and spring at 55{degrees}S. Ozone depletion rates in excess of 7% per decade occur over populated regions in the southern hemisphere poleward of 45{degrees}S for 7 months of the year. Similar rates of decrease occur during northern winter and spring over large populated regions. The enhanced zonal average ozone depletion rates at northern mid-latitudes (40-50{degrees}N) during January, February, and March, that correspond to five geographically localized regions of high ozone depletion rates, are probably associated with long-term dynamical or temperature changes. Only the equatorial band between {+-}20{degrees} shows little or no long-term ozone change since January 1979. Ozone time series data have been examined for effect of volcanic eruptions on stratospheric ozone observed by TOMS, with only the Mount Pinatubo stratospheric aerosol injection affecting ozone amounts for a few months after the eruption in June 1991. Errors caused by the short-term presence of stratospheric aerosols in the TOMS zonally averaged ozone data are less than 1% before correction, and have no significant effect on ozone trend determination. 49 refs., 6 figs., 2 tabs.

  9. [Ozone decline and UV increase].

    PubMed

    Winkler, P; Trepte, S

    2004-02-01

    The following results have been obtained from long-term observations on the ozone layer and UV at the Meteorological Observatory Hohenpeigenberg:The seasonally varying decline of the ozone layer determines the maximum exposure to UV. Since ozone decline shows the highest rates in the spring months the UV exposure has most strongly increased in this time of the year. This is especially important because in spring the human skin is not adapted to UV exposure. Weather changes from day to day can induce rapid ozone reductions in spring about -30% which in turn is followed by an increase in UV of about 40%. Clouds, especially the transparent cirrus clouds (high clouds consisting of ice particles) have increased in frequency during spring and fall while a decrease is observed in summer. This change in cloudiness reduces the daily UV dose in spring and fall while it is enhanced in summer. With increasing height above sea level UV rises by roughly 10% per 1000 m (rule of thumb). Snow reflects the UV-radiation by up to 80% enhancing the UV-doses at relevant conditions. Strong volcano eruptions destroy ozone in the stratosphere additionally during 1-2 years after the eruption. Therafter the ozone layer recovers. In April 1993, after the eruption of Mt. Pinatubo (1991), the UV burden was still 40% higher than average. Miniholes and streamers can appear unexpected on a short-time scale and cross over Central Europe within 1-2 days, thus enhancing UV irradiation. The human skin reacts to UV exposure depending on the type of skin. The campaign "Sonne(n) mit Verstand" of the Bavarian Ministries for Environment, for Health and for Education informs about the danger of UV radiation (see www.sonne-mit-ver-stand.de). The German Weather Service informs the public on present developments of the ozone layer and relevant topics byits ozone bulletin, which is also available via internet under (www.dwd.de/deFundE/Observator/MOHp/hp2/ozon/bulletin.htm).

  10. [Ozone decline and UV increase].

    PubMed

    Winkler, P; Trepte, S

    2004-02-01

    The following results have been obtained from long-term observations on the ozone layer and UV at the Meteorological Observatory Hohenpeigenberg:The seasonally varying decline of the ozone layer determines the maximum exposure to UV. Since ozone decline shows the highest rates in the spring months the UV exposure has most strongly increased in this time of the year. This is especially important because in spring the human skin is not adapted to UV exposure. Weather changes from day to day can induce rapid ozone reductions in spring about -30% which in turn is followed by an increase in UV of about 40%. Clouds, especially the transparent cirrus clouds (high clouds consisting of ice particles) have increased in frequency during spring and fall while a decrease is observed in summer. This change in cloudiness reduces the daily UV dose in spring and fall while it is enhanced in summer. With increasing height above sea level UV rises by roughly 10% per 1000 m (rule of thumb). Snow reflects the UV-radiation by up to 80% enhancing the UV-doses at relevant conditions. Strong volcano eruptions destroy ozone in the stratosphere additionally during 1-2 years after the eruption. Therafter the ozone layer recovers. In April 1993, after the eruption of Mt. Pinatubo (1991), the UV burden was still 40% higher than average. Miniholes and streamers can appear unexpected on a short-time scale and cross over Central Europe within 1-2 days, thus enhancing UV irradiation. The human skin reacts to UV exposure depending on the type of skin. The campaign "Sonne(n) mit Verstand" of the Bavarian Ministries for Environment, for Health and for Education informs about the danger of UV radiation (see www.sonne-mit-ver-stand.de). The German Weather Service informs the public on present developments of the ozone layer and relevant topics byits ozone bulletin, which is also available via internet under (www.dwd.de/deFundE/Observator/MOHp/hp2/ozon/bulletin.htm). PMID:14770335

  11. Long-Term Exposure to Ozone and Life Expectancy in the United States, 2002 to 2008.

    PubMed

    Li, Chaoyang; Balluz, Lina S; Vaidyanathan, Ambarish; Wen, Xiao-Jun; Hao, Yongping; Qualters, Judith R

    2016-02-01

    Long-term exposure to ground-level ozone is associated with increased risk of morbidity and mortality. The association remains uncertain between long-term exposure to ozone and life expectancy. We assessed the associations between seasonal mean daily 8-hour maximum (8-hr max) ozone concentrations measured during the ozone monitoring seasons and life expectancy at birth in 3109 counties of the conterminous U.S. during 2002 to 2008. We used latent class growth analysis to identify latent classes of counties that had distinct mean levels and rates of change in ozone concentrations over the 7-year period and used linear regression analysis to determine differences in life expectancy by ozone levels. We identified 3 classes of counties with distinct seasonal mean daily 8-hr max ozone concentrations and rates of change. When compared with the counties with the lowest ozone concentrations, the counties with the highest ozone concentrations had 1.7- and 1.4-year lower mean life expectancy in males and females (both P < 0.0001), respectively. The associations remained statistically significant after controlling for potential confounding effects of seasonal mean PM2.5 concentrations and other selected environmental, demographic, socio-economic, and health-related factors (both P < 0.0001). A 5 ppb higher ozone concentration was associated with 0.25 year lower life expectancy in males (95% CI: -0.30 to -0.19) and 0.21 year in females (95% CI: -0.25 to -0.17). We identified 3 classes of counties with distinct mean levels and rates of change in ozone concentrations. Our findings suggest that long-term exposure to a higher ozone concentration may be associated with a lower life expectancy.

  12. Long-Term Exposure to Ozone and Life Expectancy in the United States, 2002 to 2008

    PubMed Central

    Li, Chaoyang; Balluz, Lina S.; Vaidyanathan, Ambarish; Wen, Xiao-Jun; Hao, Yongping; Qualters, Judith R.

    2016-01-01

    Abstract Long-term exposure to ground-level ozone is associated with increased risk of morbidity and mortality. The association remains uncertain between long-term exposure to ozone and life expectancy. We assessed the associations between seasonal mean daily 8-hour maximum (8-hr max) ozone concentrations measured during the ozone monitoring seasons and life expectancy at birth in 3109 counties of the conterminous U.S. during 2002 to 2008. We used latent class growth analysis to identify latent classes of counties that had distinct mean levels and rates of change in ozone concentrations over the 7-year period and used linear regression analysis to determine differences in life expectancy by ozone levels. We identified 3 classes of counties with distinct seasonal mean daily 8-hr max ozone concentrations and rates of change. When compared with the counties with the lowest ozone concentrations, the counties with the highest ozone concentrations had 1.7- and 1.4-year lower mean life expectancy in males and females (both P < 0.0001), respectively. The associations remained statistically significant after controlling for potential confounding effects of seasonal mean PM2.5 concentrations and other selected environmental, demographic, socio-economic, and health-related factors (both P < 0.0001). A 5 ppb higher ozone concentration was associated with 0.25 year lower life expectancy in males (95% CI: −0.30 to −0.19) and 0.21 year in females (95% CI: −0.25 to −0.17). We identified 3 classes of counties with distinct mean levels and rates of change in ozone concentrations. Our findings suggest that long-term exposure to a higher ozone concentration may be associated with a lower life expectancy. PMID:26886595

  13. Long-Term Exposure to Ozone and Life Expectancy in the United States, 2002 to 2008.

    PubMed

    Li, Chaoyang; Balluz, Lina S; Vaidyanathan, Ambarish; Wen, Xiao-Jun; Hao, Yongping; Qualters, Judith R

    2016-02-01

    Long-term exposure to ground-level ozone is associated with increased risk of morbidity and mortality. The association remains uncertain between long-term exposure to ozone and life expectancy. We assessed the associations between seasonal mean daily 8-hour maximum (8-hr max) ozone concentrations measured during the ozone monitoring seasons and life expectancy at birth in 3109 counties of the conterminous U.S. during 2002 to 2008. We used latent class growth analysis to identify latent classes of counties that had distinct mean levels and rates of change in ozone concentrations over the 7-year period and used linear regression analysis to determine differences in life expectancy by ozone levels. We identified 3 classes of counties with distinct seasonal mean daily 8-hr max ozone concentrations and rates of change. When compared with the counties with the lowest ozone concentrations, the counties with the highest ozone concentrations had 1.7- and 1.4-year lower mean life expectancy in males and females (both P < 0.0001), respectively. The associations remained statistically significant after controlling for potential confounding effects of seasonal mean PM2.5 concentrations and other selected environmental, demographic, socio-economic, and health-related factors (both P < 0.0001). A 5 ppb higher ozone concentration was associated with 0.25 year lower life expectancy in males (95% CI: -0.30 to -0.19) and 0.21 year in females (95% CI: -0.25 to -0.17). We identified 3 classes of counties with distinct mean levels and rates of change in ozone concentrations. Our findings suggest that long-term exposure to a higher ozone concentration may be associated with a lower life expectancy. PMID:26886595

  14. Ozone depletion at northern and southern latitudes derived from January 1979 to December 1991 Total Ozone Mapping Spectrometer data

    NASA Technical Reports Server (NTRS)

    Herman, J. R.; Mcpeters, R.; Larko, D.

    1993-01-01

    An extended version of the Nimbus 7/TOMS ozone data set from the period January 1, 1979 to December 31, 1991 is presented. It is shown that the ozone-trend data indicate that regions of enhanced ozone depletion rates have formed at middle and high latitudes during recent years. The seasonal dependence and geographical extent of the enhanced ozone-depletion rates for the Northern and Southern hemispheres are examined. The variability of the long-term ozone trend determination is discussed via consideration of the differences among 11-, 12-, and 13-yr trend calculations. The effects of the Mount Pinatubo eruption and other volcanic eruptions on the TOMS equatorial zonal average ozone measurements, and its influence on long-term trend determinations are discussed. On the basis of a determination of the aerosol phase function using TOMS data, the effect of stratospheric aerosols on determination of ozone amounts from TOMS are shown to be less than 1 percent.

  15. Options to accelerate ozone recovery:ozone and climate benefits

    NASA Astrophysics Data System (ADS)

    Daniel, J. S.; Fleming, E. L.; Portmann, R. W.; Velders, G. J. M.; Jackman, C. H.; Ravishankara, A. R.

    2010-04-01

    Hypothetical reductions in future emissions of ozone-depleting substances (ODSs), including N2O, are evaluated in terms of effects on equivalent effective stratospheric chlorine (EESC), globally-averaged total column ozone, and radiative forcing through 2100. Due to the established success of the Montreal Protocol, these actions can have only a fraction of the impact that regulations already in force have had. If all anthropogenic ODS emissions were halted beginning in 2011, ozone is calculated to be higher by about 1-2{%} during the period 2030-2100 compared to a case of no additional ODS restrictions. Radiative forcing by 2100 would be about 0.23 W/m2 lower due to the elimination of N2O emissions and about 0.005 W/m2 lower due to destruction of the chlorofluorocarbon (CFC) bank. The ability of EESC to be a suitable metric for total ozone is also quantified. Responding to the recent suggestion that N2O should be considered an ODS, we provide an approach to incorporate N2O into the EESC formulation.

  16. Ozone reaction with interior building materials: Influence of diurnal ozone variation, temperature and humidity

    NASA Astrophysics Data System (ADS)

    Rim, Donghyun; Gall, Elliott T.; Maddalena, Randy L.; Nazaroff, William W.

    2016-01-01

    Elevated tropospheric ozone concentrations are associated with increased morbidity and mortality. Indoor ozone chemistry affects human exposure to ozone and reaction products that also may adversely affect health and comfort. Reactive uptake of ozone has been characterized for many building materials; however, scant information is available on how diurnal variation of ambient ozone influences ozone reaction with indoor surfaces. The primary objective of this study is to investigate ozone-surface reactions in response to a diurnally varying ozone exposure for three common building materials: ceiling tile, painted drywall, and carpet tile. A secondary objective is to examine the effects of air temperature and humidity. A third goal is to explore how conditioning of materials in an occupied office building might influence subsequent ozone-surface reactions. Experiments were performed at bench-scale with inlet ozone concentrations varied to simulate daytime (ozone elevated) and nighttime (ozone-free in these experiments) periods. To simulate office conditions, experiments were conducted at two temperatures (22 °C and 28 °C) and three relative humidity values (25%, 50%, 75%). Effects of indoor surface exposures were examined by placing material samples in an occupied office and repeating bench-scale characterization after exposure periods of 1 and 2 months. Deposition velocities were observed to be highest during the initial hour of ozone exposure with slow decrease in the subsequent hours of simulated daytime conditions. Daily-average ozone reaction probabilities for fresh materials are in the respective ranges of (1.7-2.7) × 10-5, (2.8-4.7) × 10-5, and (3.0-4.5) × 10-5 for ceiling tile, painted drywall, and carpet tile. The reaction probability decreases by 7%-47% across the three test materials after two 8-h periods of ozone exposure. Measurements with the samples from an occupied office reveal that deposition velocity can decrease or increase with time

  17. Ozone’s Impact on Public Health: Contributions from Indoor Exposures to Ozone and Products of Ozone-Initiated Chemistry

    PubMed Central

    Weschler, Charles J.

    2006-01-01

    Objective The associations between ozone concentrations measured outdoors and both morbidity and mortality may be partially due to indoor exposures to ozone and ozone-initiated oxidation products. In this article I examine the contributions of such indoor exposures to overall ozone-related health effects by extensive review of the literature as well as further analyses of published data. Findings Daily inhalation intakes of indoor ozone (micrograms per day) are estimated to be between 25 and 60% of total daily ozone intake. This is especially noteworthy in light of recent work indicating little, if any, threshold for ozone’s impact on mortality. Additionally, the present study estimates that average daily indoor intakes of ozone oxidation products are roughly one-third to twice the indoor inhalation intake of ozone alone. Some of these oxidation products are known or suspected to adversely affect human health (e.g., formaldehyde, acrolein, hydroperoxides, fine and ultrafine particles). Indirect evidence supports connections between morbidity/mortality and exposures to indoor ozone and its oxidation products. For example, cities with stronger associations between outdoor ozone and mortality tend to have residences that are older and less likely to have central air conditioning, which implies greater transport of ozone from outdoors to indoors. Conclusions Indoor exposures to ozone and its oxidation products can be reduced by filtering ozone from ventilation air and limiting the indoor use of products and materials whose emissions react with ozone. Such steps might be especially valuable in schools, hospitals, and childcare centers in regions that routinely experience elevated outdoor ozone concentrations. PMID:17035131

  18. Ozone-induced changes in the expression of the genes encoding regulatory enzymes for polyamine, ethylene and phenylpropanoid metabolisms in ozone tolerant and sensitive birch (Betula pendula Roth) clones

    SciTech Connect

    Talvinen, J.; Pellinen, R.; Eloranta, T.; Kangasjaervi, J. ); Julkunen-Tiitto, R. ); Karjalainen, R. )

    1993-05-01

    Increase in the atmospheric ozone concentration has been shown to affect plant growth in several ways; from decreased photosynthetic activity to visible dames and in some extreme situations even to tissue death. Plants protect themselves from the damaging effect of ozone by inducing several physiological reactions. For example, increases in ethylene production, polyamine and phenylpropanoid synthesis have been observed in stress reaction induced by increased atmospheric ozone. similar changes, which are often called general stress reactions, are induced by several other biotic and which are often called general stress reactions, are induced by several other biontic and abiotic factors, e.g., plant pathogens. It has been shown previously that the production of stress ethylene can partly be responsible for the ozone damage formation in plants. Induction of stress-polyamine synthesis can prevent ethylene formation and is higher in some ozone-tolerant plants. We have exposed ozone sensitive and resistant birch clones to ozone (150 ppb. 8 hours) to analyze ozone-induced changes in the phenylpropanoid and polyamine metabolisms and gene expression. The polyamine and phenylpropanoid contents of the experimental material are currently being analyzed and the results will be presented. We have also cloned by PCR gene probes for birch ACC-synthase, arginine decarboxylase (ADC) and phenylalanine ammoniumlyase (PAL) genes. Results will be presented where the probes have been used to analyze ozone-induced expression of the genes in the birch clones.

  19. Aircraft cabin ozone measurements on B747-100 and B747-SP aircraft: Correlations with atmospheric ozone and ozone encounter statistics

    NASA Technical Reports Server (NTRS)

    Perkins, P. J.; Holdeman, J. D.; Gauntner, D. J.

    1978-01-01

    Simultaneous measurements of atmospheric (outside) ozone concentration and ozone levels in the cabin of the B747-100 and B747-SP airliners were made by NASA to evaluate the aircraft cabin ozone contamination problem. Instrumentation on these aircraft measured ozone from an outside probe and at one point in the cabin. Average ozone in the cabin of the B747-100 was 39 percent of the outside. Ozone in the cabin of the B747-SP measured 82 percent of the outside, before corrective measures. Procedures to reduce the ozone in this aircraft included changes in the cabin air circulation system, use of the high-temperature 15th stage compressor bleed, and charcoal filters in the inlet cabin air ducting, which as separate actions reduced the ozone to 58, 19 and 5 percent, respectively. The potential for the NASA instrumented B747 aircraft to encounter high levels of cabin ozone was derived from atmospheric oxone measurements on these aircraft. Encounter frequencies for two B747-100's were comparable even though the route structures were different. The B747-SP encountered high ozone than did the B747-100's.

  20. When will the Antarctic Ozone Hole Recover?

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.; Nash, Eric R.; Kawa, S. Randolph; Montzka, Steve

    2006-01-01

    The Antarctic ozone hole develops each year and culminates by early Spring. Antarctic ozone values have been monitored since 1979 using satellite observations from the .TOMS instrument. The severity of the hole has been assessed from TOMS using the minimum total ozone value from the October monthly mean (depth of the hole) and by calculating the average size during the September-October period. Ozone is mainly destroyed by halogen catalytic cycles, and these losses are modulated by temperature variations in the collar of the polar lower stratospheric vortex. In this presentation, we show the relationships of halogens and temperature to, both the size and depth of the hole. Because atmospheric halogen levels are responding to international agreements that limit or phase out production, the amount of halogens in the stratosphere should decrease over the next few decades. Using projections of halogen levels combined with age-of-air estimates, we find that the ozone hole is recovering at an extremely slow rate and that large ozone holes will regularly recur over the next 2 decades. The ozone hole will begin to show first signs of recovery in about 2023, and the hole will fully recover to pre-1980 levels in approximately 2070. This 2070 recovery is 20 years later than recent projections.

  1. When Will the Antarctic Ozone Hole Recover?

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.; Nash, Eric R.; Kawa, S. Randolph; Montzka, Steve

    2005-01-01

    The Antarctic ozone hole develops each year and culminates by early Spring. Antarctic ozone values have been monitored since 1979 using satellite observations from the TOMS instrument. The severity of the hole has been assessed from TOMS using the minimum total ozone value from the October monthly mean (depth of the hole) and by calculating the average size during the September-October period. Ozone is mainly destroyed by halogen catalytic cycles, and these losses are modulated by temperature variations in the collar of the polar lower stratospheric vortex. In this presentation, we show the relationships of halogens and temperature to both the size and depth of the hole. Because atmospheric halogen levels are responding to international agreements that limit or phase out production, the amount of halogens in the stratosphere should decrease over the next few decades. Using projections of halogen levels combined with age-of-air estimates, we find that the ozone hole is recovering at an extremely slow rate and that large ozone holes will regularly recur over the next 2 decades. We will show estimates of both when the ozone hole will begin to show first signs of recovery, and when the hole will fully recover to pre-1980 levels.

  2. Ozone Trend Detectability

    NASA Technical Reports Server (NTRS)

    Campbell, J. W. (Editor)

    1981-01-01

    The detection of anthropogenic disturbances in the Earth's ozone layer was studied. Two topics were addressed: (1) the level at which a trend in total ozoning is detected by existing data sources; and (2) empirical evidence in the prediction of the depletion in total ozone. Error sources are identified. The predictability of climatological series, whether empirical models can be trusted, and how errors in the Dobson total ozone data impact trend detectability, are discussed.

  3. Structural changes in wood during ozonation

    NASA Astrophysics Data System (ADS)

    Ben'ko, E. M.; Manisova, O. R.; Murav'eva, G. P.; Lunin, V. V.

    2013-07-01

    It is found that ozone treatment of aspen wood leads to changes in its structural characteristics, i.e., its specific surface area and the crystallinity index of cellulose. Using optical microscopy, it is shown that ozonation is accompanied by a decrease in the average size and visible surface of wood particles. The values for the specific area of the outer surface of samples are calculated. The specific surface area available to the enzyme molecules is determined from data on the adsorption of inert protein hemoglobin on wood. It is shown that this value is an order of magnitude higher than that of the outer surface and increases considerably for an ozonized sample. Based on the results from X-ray analysis, it is established that the structure of cellulose is disordered during ozone delignification, as is indicated by a reduction in the crystallinity index and crystallite sizes.

  4. Ozone Antimicrobial Efficacy

    EPA Science Inventory

    Ozone is a potent germicide that has been used extensively for water purification. In Europe, 90 percent of the municipal water systems are treated with ozone, and in France, ozone has been used to treat drinking water since 1903. However, there is limited information on the bioc...

  5. Ozone drinking water treatment handbook

    SciTech Connect

    Rice, R.G.

    1990-01-01

    This book explains how ozone can be used to provide primary disinfection, while minimizing halogenated by-products. This is of use to those who design pilot plant studies in full scale ozone plants-and those who employ ozone and regulatory personnel. Detailed section on components of an ozonization system outlines feed gas preparation (air and oxygen), ozone generation, ozone contacting, ozone off gas destruction, monitoring and control of ozonation systems, engineering aspects of ozone, cost factors in ozone technology, case histories (European and U.S.).

  6. Monitoring and future projections of the Antarctic Ozone Hole using the new Ozone Mapping and Profiler Suite (OMPS)

    NASA Astrophysics Data System (ADS)

    Kramarova, N. A.; Newman, P. A.; Nash, E. R.; Bhartia, P. K.; McPeters, R. D.; Rault, D. F.; Seftor, C. J.; Xu, P.

    2013-12-01

    Using the new Ozone Mapping and Profiler Suite (OMPS), launched October 2011 on board the Suomi National Polar-orbiting Partnership satellite, we have studied the structure and evolution of the 2012 and 2013 ozone holes. The 1st ozone hole observations by OMPS began in 2012. We quality check the OMPS measurements by comparing to other satellite instruments (Aura MLS, OMI and SBUV) and ozone sonde balloon measurements. The comparisons reveal that OMPS is producing excellent Antarctic ozone hole information, and, thus, OMPS data can be used to continue the historical record of Antarctic ozone observations. In 2012 the ozone hole developed quite normally in the August to-late September 2012 period, but disappeared much more rapidly during the late-September to November period than it would be expected in a normal year. This resulted in the second weakest ozone hole observed since 1988. Some have suggested that the rapid 2012 disappearance is evidence that the Montreal Protocol is working. However, the development of the ozone hole in August and September is largely driven by chlorine and bromine from human-produced compounds, and the normal development of the ozone hole in August-September 2012 suggests that chlorine and bromine levels were roughly the same as previous years. At the same time, observations from meteorological data show that there were stronger than average weather systems, faster warming during the September -November period, and stronger vertical motions, that led to a rapid decay of the 2012 ozone hole. Hence, the weak ozone hole of 2012 is not evidence that the Montreal Protocol has impacted the ozone hole. The characteristics of the 2013 ozone hole, as observed by OMPS, will also be shown in the presentation. Model predictions suggest that the ozone hole will begin showing signs of recovery in about 2018, and it will be fully recovered back to 1980 levels in about 2065. We will update projections of the ozone hole recovery using a parametric model

  7. Neutron resonance averaging

    SciTech Connect

    Chrien, R.E.

    1986-10-01

    The principles of resonance averaging as applied to neutron capture reactions are described. Several illustrations of resonance averaging to problems of nuclear structure and the distribution of radiative strength in nuclei are provided. 30 refs., 12 figs.

  8. Paradoxes in Averages.

    ERIC Educational Resources Information Center

    Mitchem, John

    1989-01-01

    Examples used to illustrate Simpson's paradox for secondary students include probabilities, university admissions, batting averages, student-faculty ratios, and average and expected class sizes. Each result is explained. (DC)

  9. Response of macaque bronchiolar epithelium to ambient concentrations of ozone.

    PubMed Central

    Harkema, J. R.; Plopper, C. G.; Hyde, D. M.; St George, J. A.; Wilson, D. W.; Dungworth, D. L.

    1993-01-01

    Recently, we reported that exposure to ambient concentrations of ozone, near the U.S. National Ambient Air Quality Standard (0.12 ppm), induced significant nasal epithelial lesions in a non-human primate, the bonnet monkey. The present study defines the effects of ambient concentrations of ozone on the surface epithelium lining respiratory bronchioles and on the underlying bronchiolar interstitium in these same monkeys. Bonnet monkeys were exposed to filtered air or to 0.15 or 0.30 ppm ozone 8 hours/day for 6 or 90 days. At the end of exposures, monkeys were anesthetized and killed by exsanguination. Microdissected bronchiolar airways of infusion-fixed lungs were evaluated morphometrically by light microscopy and quantitatively by scanning and transmission electron microscopy for ozone-induced epithelial changes. Hyperplasia of nonciliated, cuboidal epithelial cells and intraluminal accumulation of macrophages characterized ozone-induced lesions in respiratory bronchioles. There were no significant differences in epithelial thickness or cell numbers among ozone-exposed groups. Ozone-exposed epithelium was composed of 80% cuboidal and 20% squamous cells compared with 40% cuboidal and 60% squamous cells in filtered air controls. In addition, the arithmetic mean thickness of the surface epithelium, a measure of tissue mass per unit area of basal lamina, was significantly increased in all of the ozone-exposed groups. The number of cuboidal epithelial cells per surface area of basal lamina was increased above control values by 780% after 6 days exposure to 0.15 ppm, 777% after 90 days to 0.15 ppm, and 996% after 90 days exposure to 0.30 ppm. There was also a significant ozone-induced increase in the thickness of the bronchiolar interstitium that was due to an increase in both cellular and acellular components. These results demonstrate that exposure to low ambient concentrations of ozone, near the current. National Ambient Air Quality Standard, induces pulmonary lesions

  10. Projections of Future Summertime Ozone over the U.S.

    SciTech Connect

    Pfister, G. G.; Walters, Stacy; Lamarque, J. F.; Fast, Jerome D.; Barth, Mary; Wong, John; Done, James; Holland, Greg; Bruyere, Cindy

    2014-05-05

    This study uses a regional fully coupled chemistry-transport model to assess changes in surface ozone over the summertime U.S. between present and a 2050 future time period at high spatial resolution (12 km grid spacing) under the SRES A2 climate and RCP8.5 anthropogenic pre-cursor emission scenario. The impact of predicted changes in climate and global background ozone is estimated to increase surface ozone over most of the U.S; the 5th - 95th percentile range for daily 8-hour maximum surface ozone increases from 31-79 ppbV to 30-87 ppbV between the present and future time periods. The analysis of a set of meteorological drivers suggests that these mostly will add to increasing ozone, but the set of simulations conducted does not allow to separate this effect from that through enhanced global background ozone. Statistically the most robust positive feedbacks are through increased temperature, biogenic emissions and solar radiation. Stringent emission controls can counteract these feedbacks and if considered, we estimate large reductions in surface ozone with the 5th-95th percentile reduced to 27-55 ppbV. A comparison of the high-resolution projections to global model projections shows that even though the global model is biased high in surface ozone compared to the regional model and compared to observations, both the global and the regional model predict similar changes in ozone between the present and future time periods. However, on smaller spatial scales, the regional predictions show more pronounced changes between urban and rural regimes that cannot be resolved at the coarse resolution of global model. In addition, the sign of the changes in overall ozone mixing ratios can be different between the global and the regional predictions in certain regions, such as the Western U.S. This study confirms the key role of emission control strategies in future air quality predictions and demonstrates the need for considering degradation of air quality with future

  11. Spatial and temporal patterns of ozone in the high elevation ecosystems of the Colorado Rocky Mountains

    NASA Astrophysics Data System (ADS)

    Liptzin, D.; Helmig, D.

    2015-12-01

    Tropospheric ozone is regulated by the US EPA to protect human health and welfare. Because the precursors to ozone formation largely come from transportation and industrial activity, ozone has typically been thought of as an urban pollution problem. However, there is growing concern about increased ozone concentrations in rural areas. Surprisingly high ozone concentrations have been measured in the high elevation Rocky Mountain ecosystems in the Front Range of Colorado. The annual median ozone mixing ratios over the past decade at three high elevation monitoring stations ranged from 47 to 53 ppbv. The hourly ozone mixing ratio typically exceeds 100 ppbv at some point every year at these sites. The number of days where the ozone mixing ratio exceeded the current 8 hour US EPA National Ambient Air Quality Standard of 75 ppb has ranged from 0 to 25 since 1987 at the monitoring site in Rocky Mountain National Park. A comparison with lower elevation sites suggests that ozone mixing ratios generally increase with elevation. In addition, the diurnal and seasonal variability of ozone decreases with elevation. Along an elevational gradient from the plains to the tundra, the tundra site had the highest median values and the least variability of any site. The seasonal pattern at these high elevation sites is also distinct as the maximum mixing ratios occur in the spring in contrast to the summer maximum typically observed in urban areas. While there have been relatively small changes in concentration in the measured data record going back a few decades, modeling suggests that ozone mixing ratios have almost doubled over the last one hundred years in Colorado. A plethora of studies has shown that elevated ozone damages foliage, with sensitive species showing effect at levels exceeding 35-40 ppbv. Since ozone levels in these high elevation ecosystems are clearly above that, we believe that they have been and will continue to be severely affected by elevated ozone. It is not

  12. Ozone and the stratosphere

    NASA Technical Reports Server (NTRS)

    Shimazaki, Tatsuo

    1987-01-01

    It is shown that the stratospheric ozone is effective in absorbing almost all radiation below 300 nm at heights below 300 km. The distribution of global ozone in the troposphere and the lower stratosphere, and the latitudinal variations of the total ozone column over four seasons are considered. The theory of the ozone layer production is discussed together with catalytic reactions for ozone loss and the mechanisms of ozone transport. Special attention is given to the anthropogenic perturbations, such as SST exhaust gases and freon gas from aerosol cans and refrigerators, that may cause an extensive destruction of the stratospheric ozone layer and thus have a profound impact on the world climate and on life.

  13. Assessing control strategies for ground level ozone

    NASA Astrophysics Data System (ADS)

    Sule, Neelesh Vijay

    2009-12-01

    combination of targeted control strategies that brings the region into attainment for the 8-hour ozone. Each day was optimized individually in sequence. In order to demonstrate applicability of the DMF 5 days (August 15, 16, 17, 18 and 19) of the episode were optimized. Although the optimization identified the key sources, time periods, and control strategies, the existing controls on these sources were not adequate to bring the region in attainment. Further reductions at these sources beyond the existing list of TCEQ/NCTCOG control strategies were required. Further modifications in the DMF for DFW were suggested to improve its performance.

  14. A global tropospheric ozone climatology from trajectory-mapped ozone soundings

    NASA Astrophysics Data System (ADS)

    Liu, G.; Liu, J. J.; Tarasick, D. W.; Fioletov, V. E.; Jin, J. J.; Moeni, O.; Liu, X.; Sioris, C. E.

    2013-05-01

    A global three-dimensional (i.e. latitude, longitude, altitude) climatology of tropospheric ozone is derived from the ozone sounding record by trajectory mapping. Approximately 52 000 ozonesonde profiles from more than 100 stations worldwide since 1962 are used. The small number of stations causes the set of ozone soundings to be sparse in geographical spacing. Here, forward and backward trajectory calculations are performed for each sounding to map ozone measurements to a number of other locations, and so to fill in the spatial domain. This is possible because the lifetime of ozone in the troposphere is of the order of weeks. This physically-based interpolation method offers obvious advantages over typical statistical interpolation methods. The trajectory-mapped ozone values show reasonable agreement, where they overlap, to the actual soundings, and the patterns produced separately by forward and backward trajectory calculations are similar. Major regional features of the tropospheric ozone distribution are clearly evident in the global maps. An interpolation algorithm based on spherical functions is further used for smoothing and to fill in remaining data gaps. The resulting three-dimensional global tropospheric ozone climatology facilitates visualization and comparison of different years, decades, and seasons, and offers some intriguing insights into the global variation of tropospheric ozone. It will be useful for climate and air quality model initialization and validation, and as an a priori climatology for satellite data retrievals. Further division of the climatology into decadal averages provides a global view of tropospheric ozone trends, which appear to be surprisingly modest over the last four decades.

  15. Spatial patterns of tropospheric ozone in the Mount Rainier region of the Cascade Mountains, USA

    USGS Publications Warehouse

    Brace, S.; Peterson, D.L.

    1998-01-01

    Few data exist on tropospheric ozone concentrations in rural and wildland areas of western Washington, U.S.A. We measured tropospheric ozone in Mount Rainier National Park and the Puget Sound region of Washington using electronic analyzers and passive samplers during the summers of 1994 and 1995. Electronic analyzers recorded hourly ozone concentrations from five locations between Seattle and Mount Rainier. Ozone concentrations generally increased with distance from Seattle, with maximum hourly concentrations recorded at Enumclaw (319 m elevation, 50 km SE of Seattle). Paradise (1650 m elevation, 100 km SE of Seattle) had the highest monthly mean concentration of all sites measured with analyzers. Diurnal patterns on high-ozone days indicate that concentrations at Paradise remain near 60 ppbv throughout the day, whereas ozone concentrations closer to Seattle had higher peaks during the afternoon but dropped to near zero at night. Passive ozone samplers were used to measure weekly average ozone exposures in four river drainages within Mount Rainier National Park, across an elevation gradient (420 a??2100 m). In most drainages, ozone levels increased with elevation, with highest average weekly ozone exposure (47 ppbv) recorded at 2100 m. Ozone concentrations are significantly higher in the western portion of the park, indicating that ozone exposure varies considerably over short distances. These data provide a reference point for air quality in western Washington and indicate that intensive sampling is necessary to quantify spatial patterns of tropospheric ozone in mountainous regions.

  16. Microbubble enhanced ozonation process for advanced treatment of wastewater produced in acrylic fiber manufacturing industry.

    PubMed

    Zheng, Tianlong; Wang, Qunhui; Zhang, Tao; Shi, Zhining; Tian, Yanli; Shi, Shanshan; Smale, Nicholas; Wang, Juan

    2015-04-28

    This work investigated microbubble-ozonation for the treatment of a refractory wet-spun acrylic fiber wastewater in comparison to macrobubble-ozonation. CODcr, NH3-N, and UV254 of the wastewater were removed by 42%, 21%, and 42%, respectively in the microbubble-ozonation, being 25%, 9%, and 35% higher than the removal rates achieved by macrobubble-ozonation at the same ozone dose. The microbubbles (with average diameter of 45μm) had a high concentration of 3.9×10(5) counts/mL at a gas flow rate of 0.5L/min. The gas holdup, total ozone mass-transfer coefficient, and average ozone utilization efficiency in the microbubble-ozonation were 6.6, 2.2, and 1.5 times higher than those of the macrobubble-ozonation. Greater generation of hydroxyl radicals and a higher zeta potential of the bubbles were also observed in the microbubble ozonation process. The biodegradability of the wastewater was also significantly improved by microbubble-ozonation, which was ascribed to the enhanced degradation of alkanes, aromatic compounds, and the many other bio-refractory organic compounds in the wastewater. Microbubble-ozonation can thus be a more effective treatment process than traditional macrobubble-ozonation for refractory wastewater produced by the acrylic fiber manufacturing industry.

  17. Microbubble enhanced ozonation process for advanced treatment of wastewater produced in acrylic fiber manufacturing industry.

    PubMed

    Zheng, Tianlong; Wang, Qunhui; Zhang, Tao; Shi, Zhining; Tian, Yanli; Shi, Shanshan; Smale, Nicholas; Wang, Juan

    2015-04-28

    This work investigated microbubble-ozonation for the treatment of a refractory wet-spun acrylic fiber wastewater in comparison to macrobubble-ozonation. CODcr, NH3-N, and UV254 of the wastewater were removed by 42%, 21%, and 42%, respectively in the microbubble-ozonation, being 25%, 9%, and 35% higher than the removal rates achieved by macrobubble-ozonation at the same ozone dose. The microbubbles (with average diameter of 45μm) had a high concentration of 3.9×10(5) counts/mL at a gas flow rate of 0.5L/min. The gas holdup, total ozone mass-transfer coefficient, and average ozone utilization efficiency in the microbubble-ozonation were 6.6, 2.2, and 1.5 times higher than those of the macrobubble-ozonation. Greater generation of hydroxyl radicals and a higher zeta potential of the bubbles were also observed in the microbubble ozonation process. The biodegradability of the wastewater was also significantly improved by microbubble-ozonation, which was ascribed to the enhanced degradation of alkanes, aromatic compounds, and the many other bio-refractory organic compounds in the wastewater. Microbubble-ozonation can thus be a more effective treatment process than traditional macrobubble-ozonation for refractory wastewater produced by the acrylic fiber manufacturing industry. PMID:25681716

  18. Mechanism and Trend Change of Sudden Increase of Total Ozone in Seoul

    NASA Astrophysics Data System (ADS)

    Cho, H.; Park, S.; Kim, J.; Lee, Y.; Mok, J.; Lee, Y.

    2009-12-01

    The total ozone column values have been observed by numerous satellites including TOMS and OMI, and extensive network of ground-based measurements (Dobson & Brewer Spectrophotometer etc.), over long time period over the globe, in which statistical long-term trend or ozone recovery are analyzed. In March 14th, 2006, sudden increase of the total ozone values are observed in East Asia, where the mixing ratio of ozone in ozonesonde data at Sapporo (14th Mar, 2006) increased between 10 and 15km remarkably. In general, stratospheric ozone does not change that abruptly. However from late winter to early spring, sudden increase of total ozone values were observed over the North-east Eurasian Continent and the Sea of Ohotsuku. In the beginning of this periods, observed total ozone values increased by more than 40~50 DU, compared with previous day’s value, maintaining abnormal condition for a few days. This mechanism is not understood clearly but in previous studies, this effect occurred by secondary ozone peak that is caused by Stratosphere-Troposphere Exchange (STE). To explain this phenomenon, we select the highest 5% of total ozone values observed in Seoul since 1985 and analyze the back trajectory and NCEP/NCAR reanalysis data between 10~20km at the same time. In the events of sudden total ozone increase, air parcels of 10~15km altitudes came mostly from arctic region, which is statistically evident. These `arctic origin air’ are ozone-rich in mixing ratio thus results in the secondary ozone peak and ozone enhancements in Seoul. These enhancements were occurred several times in a month. Thus, it changes the average of total ozone and climatological values, which affects the trend of stratospheric ozone recovery. In this study, using the ozonesonde and total ozone data, we separate the total ozone and sudden enhancement of ozone in Upper troposphere/ Lower Stratosphere and examine the effect of these changes on the ozone recovery trend in Seoul.

  19. Simultaneous measurements of ozone outside and inside cabins of two B-747 airliners and a Gates Learjet business jet

    NASA Technical Reports Server (NTRS)

    Perkins, P. J.; Briel, D.

    1978-01-01

    The average amount of ozone measured in the cabins of two B-747 airliners varied from 40 percent to 80 percent of the atmospheric concentrations without special ozone destruction systems. A charcoal filter in the cabin air inlet system of one B-747 reduced the ozone to about 5 percent of the atmospheric concentration. A Learjet 23 was also instrumented with monitors to measure simultaneously the atmospheric and ozone concentrations. Results indicate that a significant portion of the atmospheric ozone is not destroyed in the pressurization system and remains in the aircraft cabin of the Learjet. For the two cabin configurations tested, the ozone retentions were 63 and 41 percent of the atmospheric ozone concentrations. Ozone concentrations measured in the cabin near the conditioned-air outlets were reduced only slightly from atmospheric ozone concentrations. It is concluded that a constant difference between ozone concentrations inside and outside the cabin does not exist.

  20. Erythrocyte survival in sheep exposed to ozone

    SciTech Connect

    Moore, G.S.; Calabrese, E.J.; Labato, F.J.

    1981-07-01

    Erythrocyte survival studies in the Dorset ewe using chromium 51 were performed. The purpose of the study was to determine if ozone exposure produces decreased cell survival which may be the result of premature erythrocyte aging. This strain of sheep has an erythrocyte glucose-6-phosphate dehydrogenase (G6PD) activity that is very low, being comparable to human A-variants with G6PD deficiency. Ozone exposure may produce hemolytic effects in G6PD deficients more readily than in erythrocytes with normal activity. A decrease in hematocrit was observed in the ozone exposed groups. With respect to red cell destruction, ozone does not appear to act immediately, but rather there appears to be a delayed effect. At 0.25 ppM ozone, the group reached the 50% remaining level an average of 1 day sooner than the control group. There was no significant difference between control and exposed groups at the 0.50 ppM and 0.70 ppM levels. Also, the results demonstrate a net decrease in hematocrit which is greater for 0.25 ppM ozone than any other exposure level. (RJC)

  1. Interannual Variability of Ozone and Ultraviolet Exposure

    NASA Technical Reports Server (NTRS)

    Herman, J. R.; Piacentini, R. D.; Ziemke, J.; Celarier, E.; Larko. D.

    1999-01-01

    Annual zonal averages of ozone amounts from Nimbus-7/TOMS (Total Ozone Mapping Spectrometer) (1979 to 1992) are used to estimate the interannual variability of ozone and UVB (290 - 315 nm) irradiance between plus or minus 60 deg. latitude. Clear-sky interannual ozone and UVB changes are mainly caused by the Quasi Biennial Oscillation (QBO) of stratospheric winds, and can amount to plus or minus 15% at 300 nm and plus or minus 5% at 310 nm (or erythemal irradiance) at the equator and at middle latitudes. Near the equator, the interannual variability of ozone amounts and UV irradiance caused by the combination of the 2.3 year QBO and annual cycles implies that there is about a 5-year periodicity in UVB variability. At higher latitudes, the appearance of the interannual UVB maximum is predicted by the QBO, but without the regular periodicity. The 5-year periodic QBO effects on UVB irradiance are larger than the currently evaluated long-term changes caused by the decrease in ozone amounts.

  2. Adaptation to ozone: duration of effect

    SciTech Connect

    Horvath, S.M.; Gliner, J.A.; Folinsbee, L.J.

    1981-05-01

    Repeated ozone exposure induces an adaptative response whereby subsequent ozone exposure induces little or no pulmonary function change. The time course of the adaptation and the persistence of this adaptation was determined in 24 subjects. Subjects were studied for 125 min while they exercised intermittently. They were exposed to filtered air for 1 day and then in the next week for 5 consecutive days to 0.5 ppm ozone. After the fifth day, subjects were randomly assigned to return for one more ozone exposure at 1, 2, or 3 wk. The greatest decrement in FEV1 occurred on the second day of exposure. The number of consecutive ozone exposures required to produce adaptation varied from 2 to 5 days. Persistence of adaptation in ozone-sensitive subjects (initial decrease in FEV1 greater than 10%) showed marked individual variability, but the duration of adaptation was shortest for the more sensitive subjects. Adaptation, on the average, lasted for less than 2 wk, being as short as 7 days and as long as 20 days. We concluded that more sensitive subjects required more daily sequential exposures in order to adapt.

  3. 78 FR 34177 - Implementation of the 2008 National Ambient Air Quality Standards for Ozone: State Implementation...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-06-06

    ... FR 16436. \\2\\ For a detailed explanation of the calculation of the 3-year 8-hour average, see 40 CFR.... \\6\\ 77 FR 30160, May 21, 2012. In this action, the EPA proposes a rule to address the steps states... Recovery: In a separate Federal Register notice (77 FR 28772; May 16, 2012), the EPA determined...

  4. Ozone columns obtained by ground-based remote sensing in Kiev for Aura Ozone Measuring Instrument validation

    NASA Astrophysics Data System (ADS)

    Shavrina, A. V.; Pavlenko, Y. V.; Veles, A.; Syniavskyi, I.; Kroon, M.

    2007-12-01

    Ground-based observations with a Fourier transform spectrometer in the infrared region (FTIR) were performed in Kiev (Ukraine) during the time frames August-October 2005 and June-October 2006 within the Ozone Monitoring Instrument (OMI) validation project 2907 entitled "OMI validation by ground based remote sensing: ozone columns and profiles" in the frame of the international European Space Agency/Netherlands Agency for Aerospace Programmes/Royal Dutch Meteorological Institute OMI Announcement of Opportunity effort. Ozone column data for 2005 were obtained by modeling the ozone spectral band at 9.6 μm with the radiative transfer code MODTRAN3.5. Our total ozone column values were found to be lower than OMI Differential Optical Absorption Spectroscopy (DOAS) total ozone column data by 8-10 Dobson units (DU, 1 DU = 0.001 atm cm) on average, while our observations have a relatively small standard error of about 2 DU. Improved modeling of the ozone spectral band, now based on HITRAN-2004 spectral data as calculated by us, moves our results toward better agreement with the OMI DOAS total ozone column data. The observations made during 2006 with a modernized FTIR spectrometer and higher signal-to-noise ratio were simulated by the MODTRAN4 model computations. For ozone column estimates the Aqua Atmospheric Infrared Sounder satellite water vapor and temperature profiles were combined with the Aura Microwave Limb Sounder stratospheric ozone profiles and Tropospheric Emission Monitoring Internet Service-Koninklijk Nederlands Meteorologisch Instituut climatological profiles to create a priori input files for spectral modeling. The MODTRAN4 estimates of ozone columns from the 2006 observations compare rather well with the OMI total ozone column data: standard errors are of 1.11 DU and 0.68 DU, standard deviation are of 8.77 DU and 5.37 DU for OMI DOAS and OMI Total Ozone Mapping Spectrometer, respectively.

  5. Is There an Arctic Ozone Hole?

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.

    1999-01-01

    Total ozone observations from the Total Ozone Mapping Spectrometer (TOMS) instruments during March 1997 revealed an extensive region of low column densities in the Arctic region centered near the north pole. Values were below 250 Dobson units for nearly a two week period during this period, and were correlated with the position of the northern lower stratospheric polar vortex. The March 1997 average total ozone column densities were more than 30% lower than the average of column densities observed during the 1979-1982 March period. Both the northern spring seasons of 1998 and 1999 have shown much higher levels of total ozone. In this presentation, we will discuss the causes of the low total ozone values in 1997 and contrast those low values with the higher 1998 and 1999 observations. The reason for my travel to the University of Valparaiso is to give this seminar and provide information to my colleagues on our work here at GSFC. The benefit to NASA is to interact with my Univ. of Valparaiso colleagues, gain their insights and input into this research, and establish collaborations with the current research efforts at the University.

  6. Comparison of SBUV and SAGE II ozone profiles: Implications for ozone trends

    NASA Technical Reports Server (NTRS)

    Mcpeters, R. D.; Miles, T.; Flynn, L. E.; Wellemeyer, C. G.; Zawodny, J. M.

    1994-01-01

    Solar backscattered ultraviolet (SBUV) ozone profiles have been compared with Stratospheric Aerosol and Gas Experiment (SAGE) II profiles over the period October 1984 through June 1990, when data are available from both instruments. SBUV measurements were selected to closely match the SAGE II latitude/longitude measurement pattern. There are significant differences between the SAGE II sunrise and the sunset zonal mean ozone profiles in the equatorial zone, particularly in the upper stratosphere, that may be connected with extreme SAGE II solar azimuth angles for tropical sunrise measurements. Calculation of the average sunset bias between SBUV and SAGE II ozone profiles shows that allowing for diurnal variation in Umkehr layer 10, SBUV and SAGE II agree to within +/- 5% for the entire stratosphere in the northern midlatitude zone. The worst agreement is seen at southern midlatitudes near the ozone peak (disagreements of +/- 10%), apparently the result of the SBUV ozone profile peaking at a lower altitude than SAGE. The integrated ozone columns (cumulative above 15 km) agree very well, to within +/- 2.3% in all zones for both sunset and sunrise measurements. A comparison of the time dependence of SBUV and SAGE II shows that there was less than +/- 5% relative drift over the 5.5 years for all altitudes except below 25 km, where the SBUV vertical resolution is poor. The best agreement with SAGE is seen in the integrated column ozone (cumulative above 15 km), where SAGE II has a 1% negative trend relative to SBUV over the comparison period. There is a persistent disagreement of the two instruments in Umkehr layers 9 and 10 of +/- 4% over the 5.5-year comparison period. In the equatorial zone this disagreement may be caused in part by a large positive trend (0.8 K per year) in the National Meteorologica Center temperatures used to convert the SAGE II measurement of ozone density versus altitude to a pressure scale for comparison with SBUV. In the middle stratosphere (30

  7. [Ozone exposure and asthma].

    PubMed

    Kleis, S; Louis, R; Bartsch, P

    2003-03-01

    Ozone is a pollutant the production of which depends on weather conditions and car engine combustion. Numerous epidemiological studies have indicated that high ozone levels correlated with morbidity in asthma. Experimental studies have shown that exposure of healthy subjects and asthmatics to ozone levels comparable to those measured in ambient air during hot summer days can generate respiratory symptoms, neutrophilic airways inflammation and lung function impairment. Lung function changes following ozone exposure are more pronounced in asthmatics and are dependent on the duration and intensity of exposure, a previous exposure and the nutritional status of the subjects. The airway epithelial cell layer is likely to play a pivotal role in initiating the inflammatory process following ozone exposure. Control of ambient air ozone levels must be a target for public health authorities.

  8. Biological effects of ozone

    SciTech Connect

    Lippmann, M. )

    1989-09-01

    Tropospheric ozone, a classic anthropogenic air pollutant, is going to remain a troublesome byproduct of contemporary civilization for many decades. We have known for some time that the hydrocarbons and nitrogen oxides from motor vehicles, together with actinic radiation, account for local and regional photochemistry leading to prolonged afternoon ozone peaks. We also now know that agricultural burning and intensive animal husbandry elevate regional and mesoscale concentrations of ozone and its precursors, and that remote background levels of ozone have been rising steadily throughout this century. The changes we will have to make in emission controls to appreciably reduce current tropospheric ozone levels will have profound effects on our transportation systems, consumer products, and lifestyles. As a society, we will have to make difficult choices about the levels of ozone-associated health, welfare, and natural system damage we will tolerate, or conversely, how much we are willing to pay for controls which can minimize the damage.

  9. Ozone therapy in periodontics

    PubMed Central

    Gupta, G; Mansi, B

    2012-01-01

    Gingival and Periodontal diseases represent a major concern both in dentistry and medicine. The majority of the contributing factors and causes in the etiology of these diseases are reduced or treated with ozone in all its application forms (gas, water, oil). The beneficial biological effects of ozone, its anti-microbial activity, oxidation of bio-molecules precursors and microbial toxins implicated in periodontal diseases and its healing and tissue regeneration properties, make the use of ozone well indicated in all stages of gingival and periodontal diseases. The primary objective of this article is to provide a general review about the clinical applications of ozone in periodontics. The secondary objective is to summarize the available in vitro and in vivo studies in Periodontics in which ozone has been used. This objective would be of importance to future researchers in terms of what has been tried and what the potentials are for the clinical application of ozone in Periodontics. PMID:22574088

  10. The Antarctic ozone hole

    NASA Technical Reports Server (NTRS)

    Stolarski, Richard S.

    1988-01-01

    Processes that may be responsible for the thinning in the ozone layer above the South Pole are described. The chlorine catalytic cycle which destroys ozone is described, as are the major types of reactions that are believed to interfere with this cycle by forming chlorine reservoirs. The suspected contributions of polar stratospheric clouds to these processes are examined. Finally, the possibility that the ozone hole may be due more to a shift in atmospheric dynamics than to chemical destruction is addressed.

  11. Changes in stratospheric ozone.

    PubMed

    Cicerone, R J

    1987-07-01

    The ozone layer in the upper atmosphere is a natural feature of the earth's environment. It performs several important functions, including shielding the earth from damaging solar ultraviolet radiation. Far from being static, ozone concentrations rise and fall under the forces of photochemical production, catalytic chemical destruction, and fluid dynamical transport. Human activities are projected to deplete substantially stratospheric ozone through anthropogenic increases in the global concentrations of key atmospheric chemicals. Human-induced perturbations may be occurring already.

  12. Adsorption air cleaning from ozone.

    PubMed

    Baltrenas, Pranas; Paliulis, Dainius; Vasarevicius, Saulius; Simaitis, Ramutis

    2003-01-01

    Not much has been written about air cleaning from ozone. The aim of this paper was to demonstrate the possibility of adsorption air cleaning from ozone. The second aim was to investigate the dependence of the efficiency of ozone removal from the air on the height of the adsorber layer and on concentrations of ozone, and to obtain empirical formulas for calculating the efficiency of ozone treatment. Equipment for air cleaning from ozone and nitrogen and sulphur dioxides is suggested.

  13. Total ozone trend significance from space time variability of daily Dobson data

    NASA Technical Reports Server (NTRS)

    Wilcox, R. W.

    1981-01-01

    Estimates of standard errors of total ozone time and area means, as derived from ozone's natural temporal and spatial variability and autocorrelation in middle latitudes determined from daily Dobson data are presented. Assessing the significance of apparent total ozone trends is equivalent to assessing the standard error of the means. Standard errors of time averages depend on the temporal variability and correlation of the averaged parameter. Trend detectability is discussed, both for the present network and for satellite measurements.

  14. Depletion of tropospheric ozone associated with mineral dust outbreaks.

    PubMed

    Soler, Ruben; Nicolás, J F; Caballero, S; Yubero, E; Crespo, J

    2016-10-01

    From May to September 2012, ozone reductions associated with 15 Saharan dust outbreaks which occurred between May to September 2012 have been evaluated. The campaign was performed at a mountain station located near the eastern coast of the Iberian Peninsula. The study has two main goals: firstly, to analyze the decreasing gradient of ozone concentration during the course of the Saharan episodes. These gradients vary from 0.2 to 0.6 ppb h(-1) with an average value of 0.39 ppb h(-1). The negative correlation between ozone and coarse particles occurs almost simultaneously. Moreover, although the concentration of coarse particles remained high throughout the episode, the time series shows the saturation of the ozone loss. The highest ozone depletion has been obtained during the last hours of the day, from 18:00 to 23:00 UTC. Outbreaks registered during this campaign have been more intense in this time slot. The second objective is to establish from which coarse particle concentration a significant ozone depletion can be observed and to quantify this reduction. In this regard, it has been confirmed that when the hourly particle concentration recorded during the Saharan dust outbreaks is above the hourly particle median values (N > N-median), the ozone concentration reduction obtained is statistically significant. An average ozone reduction of 5.5 % during Saharan events has been recorded. In certain cases, this percentage can reach values of higher than 15 %. PMID:27376369

  15. The Impact of Increasing Carbon Dioxide on Ozone Recovery

    NASA Technical Reports Server (NTRS)

    Rosenfield, Joan E.; Douglass, Anne R.; Considine, David B.; Einaudi, Franco (Technical Monitor)

    2001-01-01

    We have used the GSFC coupled two-dimensional (2D) model to study the impact of increasing carbon dioxide from 1980 to 2050 on the recovery of ozone to its pre-1980 amounts. We find that the changes in temperature and circulation arising from increasing CO2 affect ozone recovery in a manner which varies greatly with latitude, altitude, and time of year. Middle and upper stratospheric ozone recovers faster at all latitudes due to a slowing of the ozone catalytic loss cycles. In the lower stratosphere, the recovery of tropical ozone is delayed due to a decrease in production and a speed up in the overturning circulation. The recovery of high northern latitude lower stratospheric ozone is delayed in spring and summer due to an increase in springtime heterogeneous chemical loss, and is speeded up in fall and winter due to increased downwelling. The net effect on the higher northern latitude column ozone is to slow down the recovery from late March to late July, while making it faster at other times. In the high southern latitudes, the impact of CO2 cooling is negligible. Annual mean column ozone is predicted to recover faster at all latitudes, and globally averaged ozone is predicted to recover approximately ten years faster as a result of increasing CO2.

  16. Detection and Attribution of the Recovery of Polar Ozone

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.; Nash, E. R.; Douglass, A. R.; Nielsen, J. E.; Pawson, S.; Stolarski, R. S.

    2008-01-01

    The Antarctic ozone hole develops each year and culminates by early spring (late September - early October). The severity of the hole has been assessed from satellites using the minimum total ozone value from the October monthly mean (depth of the hole), calculating the average area coverage during this September-October period, and by estimating ozone mass deficit. Profile information shows that ozone is completely destroyed in the 14-2 1 km layer by early October. Ozone is mainly destroyed by halogen (chlorine and bromine) catalytic cycles, and these losses are modulated by temperature variations. Because atmospheric halogen levels are responding to international agreements that limit or phase out production, the amount of halogens in the stratosphere should decrease over the next few decades. Both models and projections of ozone depleting substances (ODSs) into the 21St century reveal that polar ozone levels should recover in the 2060- 2070 period. In this talk, we will review current projections of polar ozone recovery. Using models and ODs projections, we explore both the past, near future (2008-2025), and far future (> 2025) levels of polar ozone. Finally, we will discuss various factors that complicate recovery such as greenhouse gas changes (e.g., cooling in the upper stratosphere) and the acceleration of the Brewer-Dobson circulation.

  17. Nimbus 7 solar backscatter ultraviolet (SBUV) ozone products user's guide

    NASA Technical Reports Server (NTRS)

    Fleig, Albert J.; Mcpeters, R. D.; Bhartia, P. K.; Schlesinger, Barry M.; Cebula, Richard P.; Klenk, K. F.; Taylor, Steven L.; Heath, Donald F.

    1990-01-01

    Three ozone tape products from the Solar Backscatter Ultraviolet (SBUV) experiment aboard Nimbus 7 were archived at the National Space Science Data Center. The experiment measures the fraction of incoming radiation backscattered by the Earth's atmosphere at 12 wavelengths. In-flight measurements were used to monitor changes in the instrument sensitivity. Total column ozone is derived by comparing the measurements with calculations of what would be measured for different total ozone amounts. The altitude distribution is retrieved using an optimum statistical technique for the inversion. The estimated initial error in the absolute scale for total ozone is 2 percent, with a 3 percent drift over 8 years. The profile error depends on latitude and height, smallest at 3 to 10 mbar; the drift increases with increasing altitude. Three tape products are described. The High Density SBUV (HDSBUV) tape contains the final derived products - the total ozone and the vertical ozone profile - as well as much detailed diagnostic information generated during the retrieval process. The Compressed Ozone (CPOZ) tape contains only that subset of HDSBUV information, including total ozone and ozone profiles, considered most useful for scientific studies. The Zonal Means Tape (ZMT) contains daily, weekly, monthly and quarterly averages of the derived quantities over 10 deg latitude zones.

  18. A global tropospheric ozone climatology from trajectory-mapped ozone soundings

    NASA Astrophysics Data System (ADS)

    Liu, G.; Liu, J.; Tarasick, D. W.; Fioletov, V. E.; Jin, J. J.; Moeini, O.; Liu, X.; Sioris, C. E.; Osman, M.

    2013-11-01

    A global three-dimensional (i.e. latitude, longitude, altitude) climatology of tropospheric ozone is derived from the ozone sounding record by trajectory mapping. Approximately 52 000 ozonesonde profiles from more than 100 stations worldwide since 1965 are used. The small number of stations results in a sparse geographical distribution. Here, forward and backward trajectory calculations are performed for each sounding to map ozone measurements to a number of other locations, and so to fill in the spatial domain. This is possible because the lifetime of ozone in the troposphere is of the order of weeks. This physically based interpolation method offers obvious advantages over typical statistical interpolation methods. The trajectory-mapped ozone values show reasonable agreement, where they overlap, to the actual soundings, and the patterns produced separately by forward and backward trajectory calculations are similar. Major regional features of the tropospheric ozone distribution are clearly evident in the global maps. An interpolation algorithm based on spherical functions is further used for smoothing and to fill in remaining data gaps. The resulting three-dimensional global tropospheric ozone climatology facilitates visualization and comparison of different years, decades, and seasons, and offers some intriguing insights into the global variation of tropospheric ozone. It will be useful for climate and air quality model initialization and validation, and as an a priori climatology for satellite data retrievals. Further division of the climatology into decadal and annual averages can provide a global view of tropospheric ozone changes, although uncertainties with regard to the performance of older sonde types, as well as more recent variations in operating procedures, need to be taken into account.

  19. Lidar measurements of stratospheric ozone during the STOIC campaign

    NASA Astrophysics Data System (ADS)

    McGee, Thomas J.; Ferrare, Richard A.; Whiteman, David N.; Butler, James J.; Burris, John F.; Owens, Melody A.

    1995-05-01

    The NASA Goddard Space Flight Center's Stratospheric Ozone Lidar Trailer Experiment participated in the Stratospheric Ozone Intercomparison Campaign (STOIC) at Table Mountain, California, from July 20 to August 2, 1989. From 20 to 39 km the average Goddard Space Flight Center (GSFC) profile agreed with the STOIC reference profile to better than 5%. The STOIC reference profile was generated by averaging all profiles from the eight participating instruments. In this same altitude region the GSFC and the Jet Propulsion Laboratory lidar average profiles also agreed to better than 5%. Similar results were found for an intercomparison of the lidar data with ozone data from ECC sondes launched from Table Mountain and from San Nicholas Island. The results of the intercomparison have led to a number of modifications to the GSFC lidar which have greatly improved the reliability of the ozone data, particularly at altitudes below 20 km and above 40 km.

  20. Lidar measurements of stratospheric ozone during the STOIC campaign

    SciTech Connect

    McGee, T.J.; Burris, J.F.; Ferrare, R.A.

    1995-05-20

    The NASA Goddard Space Flight Center`s Stratospheric Ozone Lidar Trailer Experiment participated in the Stratospheric Ozone Intercomparison Campaign (STOIC) at Table Mountain, California, from July 20 to August 2, 1989. From 20 to 39 km the average Goddard Space Flight Center (GSFC) profile agreed with the STOIC reference profile to better than 5%. The STOIC reference profile was generated by averaging all profiles from the eight participating instruments. In this same altitude region the GSFC and the Jet Propulsion Laboratory lidar average profiles also agreed to better than 5%. Similar results were found for an intercomparison of the lidar data with ozone data from EC sondes launched from Table Mountain and from San Nicholas Island. The results of the intercomparison have led to a number of modifications to the GSFC lidar which have greatly improved the reliability of the ozone data, particularly at altitudes below 20 km and above 40 km. 10 refs., 9 figs.

  1. Occurrence of ozone as a phytotoxicant in Kiev, Ukraine and in the Ukrainian Carpathian mountains

    SciTech Connect

    Bytnerowicz, A.; Manning, W.; Blum, O.; Popovicheva, L.

    1995-12-31

    Ogawa passive ozone samplers were established at the Central Botanic Garden in Kiev and in five forest locations in the Ukrainian Carpathian mountains in summer, 1995. An active ozone monitor (Thermo-Electron 49) was also established at the Botanic Garden, together with plants of ozone-sensitive (Bel-W3) and ozone-tolerant (Bel-B) tobacco (Nicotiana tabacum). The highest average hourly ozone concentration monitored in Kiev was 84.4 ppb. From August to September, two-week average concentrations of ozone (Ogawa samplers) in the Carpathian forests ranged from 27.4--51.8 ppb. During a two-week exposure period, Bel-W3 tobacco plants in Kiev had foliar injury on leaf one as high as 62%, with only 13% for Bel-B. Ozone injury was found on a variety of indicator plants in Kiev and at three of the five passive sampler sites in the Carpathians.

  2. Biomonitoring of tropospheric ozone phytotoxicity in rural Catalonia

    NASA Astrophysics Data System (ADS)

    Ribas, Angela; Peñuelas, Josep

    The ozone (O 3) phytotoxicity in rural areas of Catalonia (NE Spain) and the biomonitoring capacity of Bel-W3 tobacco ( Nicotiana tabacum) cultivars were assessed by determining the percentage of leaf area injured by ozone in plants of this cultivar exposed from spring to autumn since 1995-1999. The study was conducted simultaneously on nine field sites where ground level ozone concentrations and meteorological parameters were continuously monitored. Geographical, seasonal and annual variations of ozone damage rate and their links with meteorological conditions were studied. Ozone concentrations and leaf damage increased at the end of spring and the beginning of summer. Coastal sites generally presented higher O 3 concentrations than inland and mountain sites. These mountain sites were the most sensitive ones to ozone toxicity. The ozone concentrations correlated well with ozone injury. However, at this local scale the ozone levels did not fully account for all the observed injury (only 11%). The response of tobacco plants to ozone concentrations and therefore its biomonitoring capacity depended also on different environmental conditions, mainly those linked to stomatal behaviour such as vapour pressure deficit. The categorization of leaf damage in 10% intervals and its averaging throughout the whole study period and the whole region, strongly improved (99% of variance accounted) the relationship with ozone concentrations expressed as AOT20 (accumulated over a cut-off of 20 ppb v). N. tabacum cultivar Bel-W3 is thus a very good biomonitor of ozone concentrations in the long term at the regional scale. Taking into account the phytotoxical response of this sensitive tobacco cultivar, we propose the 1.28 ppm v h biweekly AOT40 (with a solar radiation threshold of 50 W m -2) as a damage threshold level for sensitive species.

  3. Results of ozone measurements in Northern Germany: A case study

    NASA Technical Reports Server (NTRS)

    Schmidt, Manfred

    1994-01-01

    At most of the German ozone recording stations which have records over a sufficiently long period, the results of the summer months of 1989 showed the highest values since the beginning of the measurements. One of the reasons for this phenomenon was the high duration of sunshine in that summer; for example, in Potsdam near Berlin in May 1989 the sunshine duration was the highest in May since the beginning of the records in 1893. For that reason we selected this summer for a case study. The basis for the study was mainly the ozone measuring stations of the network of Lower Saxony and the Federal Office of Environment (Umweltbundesamt). The results of these summer measurements point to intense sources of ozone, probably in form of gaseous precursors, in the Middle German industrial areas near Leipzig and Halle and in Northwestern Czechoslovakia, with coal-mining, chemical and petrochemical industries, coking plants and others. The maps of average ozone concentrations, number or days with high ozone maxima, ozone-windroses of the stations, etc., suggest that these areas could be a main source of precursors and of photochemical ozone production in summer smog episodes in Central Europe. Stations on the North Sea coast, at which early ozone measurements were made by our institute in 1973/74 are compared with similarly located stations of the Lower Saxon network in 1989 and the results show a reversal of the ozone-windroses. In 1973/74, the highest ozone concentrations were correlated with wind directions from the sea while in 1989 these concentrations were correlated with directions from the continent. In the recent years, photochemical ozone production on the continent is probably predominant, while in former years the higher ozone content of the maritime subpolar air masses has been explained by stratospheric-tropospheric exchange.

  4. A Holistic Evaluation of the Houston, Texas Ozone Attainment Episode

    NASA Astrophysics Data System (ADS)

    Biton, L.; Vizuete, W.; Kim, B.; Jeffries, H. E.

    2006-12-01

    In early 2006, the Texas Commission on Environmental Quality (TCEQ) released a simulation episode to form the basis for its 8-Hour Ozone State Implementation Plan (SIP). The SIP details steps to be taken to bring the Houston-Galveston-Brazoria region into attainment of the National Ambient Air Quality Standard for ozone (O3). The modeling episode will have significant impacts on regulatory decision-making, thus affecting the regional economy and human health. At present model performance evaluations (MPEs) are based on guidelines set by the Environmental Protection Agency (EPA) that rely heavily on statistical measures. While the episode falls within the recommended range for these EPA statistical metrics, examining the level of agreement between model predictions and observations for O3 is not a sufficient method to assess model accuracy. We have discovered severe inaccuracies in the 8-Hour modeling episode with an evaluation methodology that recognizes that (1) the formation of tropospheric O3 system is non-linear with respect to its precursors and (2) is the result of a multitude of chemical, emission, and meteorological processes. This paper presents the results of this improved evaluation method using new tools and software developed at the University of North Carolina at Chapel Hill. These tools were designed specifically to compensate for inadequacies in the existing statistical methods currently used for MPE. These tools enable investigators to review O3 production and concentrations in the context of meteorological and chemical conditions, allowing more holistic analytical techniques, not captured by traditional statistical metrics. In our analysis all modeling results are compared with high-resolution data from multiple sources, including an extensive ground-monitoring network, automatic gas-chromatographs (auto-GCs), and aircraft. First in our investigation, as a measure of progress, the latest 8-Hour episode is compared to TCEQ"s previous 1-Hour O3 SIP

  5. Tropospheric ozone in the Nisqually River Drainage, Mount Rainier National Park

    USGS Publications Warehouse

    Peterson, D.L.; Bowers, Darci

    1999-01-01

    We quantified the summertime distribution of tropospheric ozone in the topographically complex Nisqually River drainage of Mount Rainier National Park from 1994 to 1997. Passive ozone samplers were used along an elevational transect to measure weekly average ozone concentrations ranging from 570 m to 2040 m elevation. Weekly average ozone concentrations were positively correlated with elevation, with the highest concentrations consistently measured at the highest sampling site (Panorama Point). Weekly average ozone concentrations at Mount Rainier National Park are considerably higher than those in the Seattle-Tacoma metropolitan area to the west. The anthropogenic contribution to ozone within the Nisqually drainage was evaluated by comparing measurements at this location with measurements from a 'reference' site in the western Olympic Mountains. The comparison suggests there is a significant anthropogenic source of ozone reaching the Cascade Range via atmospheric transport from urban areas to the west. In addition. temporal (week to week) variation in ozone distribution is synchronous within the Nisqually drainage, which indicates that subregional patterns are detectable with weekly averages. The Nisqually drainage is likely the 'hot spot' for air pollution in Mount Rainier National Park. By using passive ozone samplers in this drainage in conjunction with a limited number of continuous analyzers, the park will have a robust monitoring approach for measuring tropospheric ozone over time and protecting vegetative and human health.

  6. The Antarctic Ozone Hole.

    ERIC Educational Resources Information Center

    Stolarski, Richard S.

    1988-01-01

    Discusses the Airborne Antarctic Ozone Experiment (1987) and the findings of the British Antarctic Survey (1985). Proposes two theories for the appearance of the hole in the ozone layer over Antarctica which appears each spring; air pollution and natural atmospheric shifts. Illustrates the mechanics of both. Supports worldwide chlorofluorocarbon…

  7. Surface Ozone in Kiev

    NASA Astrophysics Data System (ADS)

    Shavrina, A. V.; Mikulskaya, I. A.; Kiforenko, S. I.; Blum, O. B.; Sheminova, V. A.; Veles, A. A.

    The study of total ozone over Kiev and its concentration changes with height in the troposphere has been made on the base of ground-based observations with the infrared Fourier-spectrometer in the Main Astronomical Observatory of National Academy of Sciences of Ukraine (MAO NASU) as part of ESA-NIVR-KNMI project no 2907 "OMI validation by ground based remote sensing: ozone columns and atmospheric profiles "(2005-2008) [1,2,4]. Ground-level ozone in Kiev for an episode of its high concentrations in August 2000 was also simulated with the model of urban air pollution UAM-V [5,6]. In 2008 the satellite data Aura-OMI on profiles of ozone in the atmosphere OMO3PR became available (http://disc.sci.gsfc.nasa.gov/ Aura/data-holdings/OMI/ omo3pr_v003.shtml). They include ozone content in the lower layer of the atmosphere, beginning from 2005, which can be used to evaluate the ground-level ozone in all cities of Ukraine. The comparison of the data of ozone air pollution in Kiev (ozone - the pollutant of the first class of danger) and medical statistics data of of respiratory system (RS) diseases of the city population was carried out with the package "Statistica". A regression analysis, prognostic regression modelling, and retrospective prognosis of the epidemiological situation with respect to RS pathologies in Kiev in 2000-2006 were performed.

  8. Ozone and temperature trends

    NASA Technical Reports Server (NTRS)

    Stolarski, Richard S.; Fioletov, Vitali; Bishop, Lane; Godin, Sophie; Bojkov, Rumen D.; Kirchhoff, Volker; Chanin, Marie-Lise; Zawodny, Joseph M.; Zerefos, Christos S.; Chu, William

    1991-01-01

    An update of the extensive reviews of the state of knowledge of measured ozone trends published in the Report of the International Ozone Trends Panel is presented. The update contains a review of progress since these reports, including reviewing of the ozone records, in most cases through March 1991. Also included are some new, unpublished reanalyses of these records including a complete reevaluation of 29 stations located in the former Soviet Union. The major new advance in knowledge of the measured ozone trend is the existence of independently calibrated satellite data records from the Total Ozone Mapping Spectrometer (TOMS) and Stratospheric Aerosol and Gas Experiment (SAG) instruments. These confirm many of the findings, originally derived from the Dobson record, concerning northern mid-latitude changes in ozone. We now have results from several instruments, whereas the previously reported changes were dependent on the calibration of a single instrument. This update will compare the ozone records from many different instruments to determine whether or not they provide a consistent picture of the ozone change that has occurred in the atmosphere. The update also briefly considers the problem of stratospheric temperature change. As in previous reports, this problem received significantly less attention, and the report is not nearly as complete. This area needs more attention in the future.

  9. Saving Our Ozone Shield.

    ERIC Educational Resources Information Center

    Lacoste, Beatrice

    1992-01-01

    Discusses the introduction and continued use of chlorofluorocarbons (CFCs) as related to stratospheric ozone depletion. Presents the characteristics of CFCs conducive to the chemical reaction with ozone, the history of CFC use and detection of related environmental problems, health hazards, and alternatives to CFC use. (MCO)

  10. Polar Ozone Workshop. Abstracts

    NASA Technical Reports Server (NTRS)

    Aikin, Arthur C.

    1988-01-01

    Results of the proceedings of the Polar Ozone Workshop held in Snowmass, CO, on May 9 to 13, 1988 are given. Topics covered include ozone depletion, ozonometry, polar meteorology, polar stratospheric clouds, remote sensing of trace gases, atmospheric chemistry and dynamical simulations.

  11. The average enzyme principle.

    PubMed

    Reznik, Ed; Chaudhary, Osman; Segrè, Daniel

    2013-09-01

    The Michaelis-Menten equation for an irreversible enzymatic reaction depends linearly on the enzyme concentration. Even if the enzyme concentration changes in time, this linearity implies that the amount of substrate depleted during a given time interval depends only on the average enzyme concentration. Here, we use a time re-scaling approach to generalize this result to a broad category of multi-reaction systems, whose constituent enzymes have the same dependence on time, e.g. they belong to the same regulon. This "average enzyme principle" provides a natural methodology for jointly studying metabolism and its regulation.

  12. Observing trends in total ozone and extreme ozone events

    NASA Astrophysics Data System (ADS)

    Balcerak, Ernie

    2014-05-01

    The ozone layer in the stratosphere has been recovering since the 1989 Montreal Protocol reduced the use of ozone-destroying chlorofluorocarbons. Fitzka et al. observed trends in total ozone levels and the vertical distribution of ozone at Hoher Sonnblick, a mountain in Austria, from 1994 to 2011.

  13. Distinctive timing of U.S. historical ozone change determined by climate and anthropogenic emissions

    NASA Astrophysics Data System (ADS)

    Yan, Y.; Lin, J.; He, C.

    2015-12-01

    The ground-level ozone over the United States is known to have been influenced by historical climate change and anthropogenic precursor emissions, whereas their individual contributions and the associated mechanisms of influence remain less understood. Here we analyze 25-year (1990-2014) annual mean ground-level ozone across the U.S. Empirical Orthogonal Function (EOF) and linear fitting show that ozone has experienced a notable rate of growth at 0.13 ppb/yr averaged over U.S. About 74% of this growth is attributed to enhancement in nighttime ozone (at 0.19 ppb/yr), with the remaining 26% due to daytime ozone increase (at 0.07 ppb/yr). To relate ozone interannual variations to climate change, we employ the Atlantic Multi-decadal Oscillation (AMO) and Southern Oscillation (SO) indices to infer the states of climate over the U.S. We find large correlations between ozone interannual variability and these climate indices: 0.65 for SO index, 0.73 for AMO index, and 0.82 for their combined index. The correlations are much higher (0.69, 0.78 and 0.86) for daytime ozone. Sensitivity simulations conducted with the GEOS-Chem chemical transport model reveal that climate variability has determined ozone interannual variability, particularly for daytime ozone, while anthropogenic emissions reductions have particularly driven the growth in nighttime ozone. These results better connect ozone air pollution with human activity and climate change. Figure. Slopes for the linear fitting analyse of the ground-level ozone variations on the inter-annual timescale for AQS measurements during 1990-2014 (a) for daytime ozone and (b) for nighttime ozone. Also shown are the slopes for interannual variation during 2004-2011 (c) for daytime ozone and (d) for nighttime ozone.

  14. Climate-chemistry interaction affecting tropospheric ozone

    NASA Astrophysics Data System (ADS)

    Mao, Huiting

    1999-09-01

    Tropospheric ozone, an important radiative-chemical species, has been observed increasing especially at northern midlatitudes during the past few decades. This dissertation addresses climate-chemistry interaction associated with such increases in three aspects using observations as well as atmospheric chemistry and climate models. Ozone impact on climate is first evaluated by radiative forcing calculations due to observed ozone changes. It is found that a 10% increase in tropospheric ozone causes a radiative forcing of 0.17 Wm-2 using a fixed temperature (FT) method or 0.13 Wm-2 using a fixed dynamic heating (FDH) method, which is comparable to the radiative forcing 0.26 (FT) and -0.09 Wm-2 (FDH) caused by the stratospheric ozone depletion during the 1980s. Second, radiative forcing due to changes in ozone precursors is estimated. Ozone changes in response to a 20% reduction in surface NOx emission in six regions around the globe differ between regions. A maximum decrease in ozone column reaches 5% in southeast Asia and the central Atlantic Ocean, inducing a local radiative forcing of up to -0.1 Wm-2 in those regions. It indicates that surface NOx emission changes can potentially affect regional climate. Third, the effects of climate and climate changes on atmospheric chemistry are addressed with two studies. One study investigates the effects of global warming on methane and ozone, and another looks into cloud effects on photodissociation rate constants. Calculations based on the IPCC business-as-usual scenario indicate that by 2050, temperature and moisture increases can suppress methane and tropospheric ozone increases by 17% and 11%, respectively, in reference to the 1990 concentrations. The combined effects offset the global warming induced forcing 3.90 Wm -2 by -0.46 Wm-2. A one-dimensional study suggests that a typical cirrus cloud (τ = 2) can significantly increase J(O1D) and J(NO2) around the tropopause with a maximum of 21%. Geographical and seasonal

  15. Ozone in equatorial latitudes

    NASA Astrophysics Data System (ADS)

    Martini, L.; Zimmermann, G.; Trinkkeller, B.

    The presence of ozone in the atmosphere protects the biosphere against harmful solar UV radiation. The ozone distribution in the atmosphere is maintained on the basis of a complex system of reactions. The amount of atmospheric ozone might be reduced as a consequence of human activities. Such reduction in the atmospheric ozone could affect climate and biological processes on earth. As a part of plans for a further enhancement of the global surveillance of the atmospheric ozone layer, a series of radiation experiments concerning the quartz-ultraviolet region were conducted as a joint project of the German Democratic Republic and the USSR. The experiments had the objective to measure the radiative flux of the solar UV radiation and to determine absorption and dispersion of the radiation in the upper atmosphere. The investigation included the launching of 12 rockets from a research vessel in the Indian Ocean near the equator and 34 balloon flights.

  16. Estimating contribution of wildland fires to ambient ozone levels in National Parks in the Sierra Nevada, California.

    PubMed

    Preisler, Haiganoush K; Zhong, Shiyuan Sharon; Esperanza, Annie; Brown, Timothy J; Bytnerowicz, Andrzej; Tarnay, Leland

    2010-03-01

    Data from four continuous ozone and weather monitoring sites operated by the National Park Service in Sierra Nevada, California, are used to develop an ozone forecasting model and to estimate the contribution of wildland fires on ambient ozone levels. The analyses of weather and ozone data pointed to the transport of ozone precursors from the Central Valley as an important source of pollution in these National Parks. Comparisons of forecasted and observed values demonstrated that accurate forecasts of next-day hourly ozone levels may be achieved by using a time series model with historic averages, expected local weather and modeled PM values as explanatory variables. Results on fire smoke influence indicated occurrence of significant increases in average ozone levels with increasing fire activity. The overall effect on diurnal ozone values, however, was small when compared with the amount of variability attributed to sources other than fire.

  17. Estimating contribution of wildland fires to ambient ozone levels in National Parks in the Sierra Nevada, California.

    PubMed

    Preisler, Haiganoush K; Zhong, Shiyuan Sharon; Esperanza, Annie; Brown, Timothy J; Bytnerowicz, Andrzej; Tarnay, Leland

    2010-03-01

    Data from four continuous ozone and weather monitoring sites operated by the National Park Service in Sierra Nevada, California, are used to develop an ozone forecasting model and to estimate the contribution of wildland fires on ambient ozone levels. The analyses of weather and ozone data pointed to the transport of ozone precursors from the Central Valley as an important source of pollution in these National Parks. Comparisons of forecasted and observed values demonstrated that accurate forecasts of next-day hourly ozone levels may be achieved by using a time series model with historic averages, expected local weather and modeled PM values as explanatory variables. Results on fire smoke influence indicated occurrence of significant increases in average ozone levels with increasing fire activity. The overall effect on diurnal ozone values, however, was small when compared with the amount of variability attributed to sources other than fire. PMID:19914752

  18. Record low global ozone in 1992

    SciTech Connect

    Gleason, J.F. ); Bhartia, P.K.; Herman, J.R.; McPeters, R.; Newman, P.; Stolarski, R.S. ); Flynn, L. ); Labow, G.; Larko, D.; Seftor, C.; Wellemeyer, C. ); Komhyr, W.D. ); Miller, A.J.; Planet, W. )

    1993-04-23

    The 1992 global average total ozone, measured by the Total Ozone Mapping Spectrometer (TOMS) on the Nimbus-7 satellite, was 2 to 3 percent lower than any earlier year observed by TOMS (1979 to 1991). Ozone amounts were low in a wide range of latitudes in both the Northern and Southern hemispheres, and the largest decreases were in the regions from 10[degrees]S to 20[degrees]S and 10[degrees]N to 60[degrees]N. Global ozone in 1992 is at least 1.5 percent lower than would be predicted by a statistical model that includes a linear trend and accounts for solar cycle variation and the quasi-biennial oscillation. These results are confirmed by comparisons with data from other ozone monitoring instruments: the SBUV/2 instrument on the NOAA-11 satellite, the TOMS instrument on the Russian Meteor-3 satellite, the World Standard Dobson instrument 83, and a collection of 22 ground-based Dobson instruments.

  19. The Hole in the Ozone Layer.

    ERIC Educational Resources Information Center

    Hamers, Jeanne S.; Jacob, Anthony T.

    This document contains information on the hole in the ozone layer. Topics discussed include properties of ozone, ozone in the atmosphere, chlorofluorocarbons, stratospheric ozone depletion, effects of ozone depletion on life, regulation of substances that deplete the ozone layer, alternatives to CFCs and Halons, and the future of the ozone layer.…

  20. A national fine spatial scale land-use regression model for ozone.

    PubMed

    Kerckhoffs, Jules; Wang, Meng; Meliefste, Kees; Malmqvist, Ebba; Fischer, Paul; Janssen, Nicole A H; Beelen, Rob; Hoek, Gerard

    2015-07-01

    Uncertainty about health effects of long-term ozone exposure remains. Land use regression (LUR) models have been used successfully for modeling fine scale spatial variation of primary pollutants but very limited for ozone. Our objective was to assess the feasibility of developing a national LUR model for ozone at a fine spatial scale. Ozone concentrations were measured with passive samplers at 90 locations across the Netherlands (19 regional background, 36 urban background, 35 traffic). All sites were measured simultaneously during four 2-weekly campaigns spread over the seasons. LUR models were developed for the summer average as the primary exposure and annual average using predictor variables obtained with Geographic Information Systems. Summer average ozone concentrations varied between 32 and 61 µg/m(3). Ozone concentrations at traffic sites were on average 9 µg/m(3) lower compared to regional background sites. Ozone correlated highly negatively with nitrogen dioxide and moderately with fine particles. A LUR model including small-scale traffic, large-scale address density, urban green and a region indicator explained 71% of the spatial variation in summer average ozone concentrations. Land use regression modeling is a promising method to assess ozone spatial variation, but the high correlation with NO2 limits application in epidemiology.

  1. The 2010 Antarctic ozone hole: observed reduction in ozone destruction by minor sudden stratospheric warmings.

    PubMed

    de Laat, A T J; van Weele, M

    2011-01-01

    Satellite observations show that the 2010 Antarctic ozone hole is characterized by anomalously small amounts of photochemical ozone destruction (40-60% less than the 2005-2009 average). Observations from the MLS instrument show that this is mainly related to reduced photochemical ozone destruction between 20-25 km altitude. Lower down between 15-20 km the atmospheric chemical composition and photochemical ozone destruction is unaffected. The modified chemical composition and chemistry between 20-25 km altitude in 2010 is related to the occurrence of a mid-winter minor Antarctic Sudden Stratospheric Warming (SSW). The measurements indicate that the changes in chemical composition are related to downward motion of air masses rather than horizontal mixing, and affect stratospheric chemistry for several months. Since 1979, years with similar anomalously small amounts of ozone destruction are all characterized by either minor or major SSWs, illustrating that their presence has been a necessary pre-condition for reduced Antarctic stratospheric ozone destruction. PMID:22355557

  2. Fundamentals of ISCO Using Ozone

    EPA Science Inventory

    In situ chemical oxidation (ISCO) using ozone involves the introduction of ozone gas (O3) into the subsurface to degrade organic contaminants of concern. Ozone is tri-molecular oxygen (O2) that is a gas under atmospheric conditions and is a strong oxidant. Ozone may react with ...

  3. The Two Faces of Ozone.

    ERIC Educational Resources Information Center

    Monastersky, Richard

    1989-01-01

    Provides answers to questions regarding the ozone problem: (1) nature of ozone in the troposphere and stratosphere; (2) possibility of sending the excess ozone at ground level to the stratosphere; (3) possibility of producing pure ozone and carrying it to the stratosphere; and (4) banning chlorofluorocarbons. (YP)

  4. Projecting policy-relevant metrics for high summertime ozone pollution events over the eastern United States due to climate and emission changes during the 21st century

    NASA Astrophysics Data System (ADS)

    Rieder, Harald E.; Fiore, Arlene M.; Horowitz, Larry W.; Naik, Vaishali

    2015-01-01

    the eastern United States (EUS), nitrogen oxides (NOx) emission controls have led to improved air quality over the past two decades, but concerns have been raised that climate warming may offset some of these gains. Here we analyze the effect of changing emissions and climate, in isolation and combination, on EUS summertime surface ozone (O3) over the recent past and the 21st century in an ensemble of simulations performed with the Geophysical Fluid Dynamics Laboratory CM3 chemistry-climate model. The simulated summertime EUS O3 is biased high but captures the structure of observed changes in regional O3 distributions following NOx emission reductions. We introduce a statistical bias correction, which allows derivation of policy-relevant statistics by assuming a stationary mean state bias in the model, but accurate simulation of changes at each quantile of the distribution. We contrast two different 21st century scenarios: (i) representative concentration pathway (RCP) 4.5 and (ii) simulations with well-mixed greenhouse gases (WMGG) following RCP4.5 but with emissions of air pollutants and precursors held fixed at 2005 levels (RCP4.5_WMGG). We find under RCP4.5 no exceedance of maximum daily 8 hour average ozone above 75 ppb by mid-21st century, reflecting the U.S. NOx emissions reductions projected in RCP4.5, while more than half of the EUS exceeds this level by the end of the 21st century under RCP4.5_WMGG. Further, we find a simple relationship between the changes in estimated 1 year return levels and regional NOx emission changes, implying that our results can be generalized to estimate changes in the frequency of EUS pollution events under different regional NOx emission scenarios.

  5. Greenhouse gases and recovery of the Earth's ozone layer

    NASA Astrophysics Data System (ADS)

    Dyominov, I. G.; Zadorozhny, A. M.

    A numerical two-dimension zonally average interactive dynamical radiative-photochemical model of the atmosphere is used for investigation the role of the greenhouse gases CO2, CH4, and N2O in the recovery of the Earth's ozone layer after reduction of anthropogenic discharges in the atmosphere of chlorine and bromine compounds. The model allows calculating self-consistently diabatic circulation, temperature, gaseous composition of the troposphere and stratosphere at latitudes from the South to North Poles, as well as distribution of sulphate aerosol particles and polar stratospheric clouds of types I and II. The scenarios of future changes of the greenhouse gases and chlorine and bromine species are taken from Climate Change 1995. The calculations show that expected cooling of the stratosphere caused by the increasing of the greenhouse gases, particularly CO2, enhances the ozone concentration in the stratosphere due to a weakness of the efficiencies of all catalytic cycles of the ozone destruction caused by temperature dependencies of photochemical reactions. The result of this effect is a significant acceleration of the ozone layer recovery after reduction of anthropogenic discharges in the atmosphere of chlorine and bromine species. On the other hand, the cooling of the stratosphere intensifies a formation of the polar stratospheric clouds in the lower stratosphere in the Polar Regions. Heterogeneous reactions on the polar stratospheric clouds, which are the key processes in the destruction of the ozone layer at the high latitudes, lead to more intensive ozone depletion here, which causes a delay of the ozone layer recovery. The calculations show that this effect is weaker than the first one so that the global ozone will recover faster under conditions of continuing anthropogenic growth of the greenhouse gases. The model predicts in this case that the annual average global ozone will reach its undisturbed level of 1980 by about 2040. If the growth of the

  6. Ozone measurements in Amazonia: Dry season versus wet season

    SciTech Connect

    Kirchhoff, V.W.J.H. ); Da Silva, I.M.O. ); Browell, E.V. )

    1990-09-20

    Observations were made almost continuously at the surface, and in addition, 20 ozone profiles were obtained in the troposphere and stratosphere. These ozone measurements were part of a field expedition to the Brazilian Amazon region, the ABLE 2B mission, a joint American-Brazilian effort to measure local concentrations of several species relevant to atmospheric chemistry. The time period of this expedition was April-May 1987, during the local wet season. For the surface ozone data the measurement technique sued was UV absorption. Ozone profiles were obtained with electrochemical concentration cell sondes, launched on balloons. The major site of operation was set up near Manaus (3{degree}S, 60{degree}W). The results are presented and compared with a previous dry season experiment. Surface ozone mixing ratios show diurnal variations that have maxima in the daytime and minima at night. The diurnal maximum at noontime, considered very low (12 ppbv) in the dry season was even lower in this wet season period (6 ppbv). A significant difference can be seen between clearing and forest data, and between different height levels above the surface, showing the existence of a large positive gradient of ozone with height. The ozone profiles in the troposphere show that there is less ozone not only at the surface but in the whole troposphere, with the wet season average showing between 6 and 12 ppbv less ozone. This difference is much smaller in the stratosphere, where there is slightly more ozone in the region of the peak, during the wet season. An isolated shower or thunderstorm in the dry season could produce transient ozone variations (mixing ratio increases or decreases) that were not observed in the wet season.

  7. Average density in cosmology

    SciTech Connect

    Bonnor, W.B.

    1987-05-01

    The Einstein-Straus (1945) vacuole is here used to represent a bound cluster of galaxies embedded in a standard pressure-free cosmological model, and the average density of the cluster is compared with the density of the surrounding cosmic fluid. The two are nearly but not quite equal, and the more condensed the cluster, the greater the difference. A theoretical consequence of the discrepancy between the two densities is discussed. 25 references.

  8. Estimating when the Antarctic Ozone Hole will Recover

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.; Nash, Eric R.; Douglass, Anne R.; Nielsen, J. Eric; Pawson, Steven; Stolarski, Richard S.

    2007-01-01

    The Antarctic ozone hole develops each year and culminates by early spring (late September - early October). The severity of the hole has been assessed from satellites using the minimum total ozone value from the October monthly mean (depth of the hole) and by calculating the average area coverage during this September-October period. Profile information shows that ozone is completely destroyed in the 14-2 1 km layer by early October. Ozone is mainly destroyed by halogen (chlorine and bromine) catalytic cycles, and these losses are modulated by temperature variations. Because atmospheric halogen levels are responding to international a'greements that limit or phase out production, the amount of halogens in the stratosphere should decrease over the next few decades. Using projections of halogen levels combined with age-of-air estimates, we find that the ozone hole is recovering at an extremely slow rate and that large ozone holes will regularly recur over the next 2 decades. We estimate that the ozone hole will begin to show first signs of size decrease in about 2023, and the hole will fully recover to pre-1980 levels in approximately 2070. Estimates of the ozone hole's recovery from models reveal important differences that will be discussed.

  9. Estimating When the Antarctic Ozone Hole Will Recover

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.; Nash, Eric R.; Douglass, Anne R.; Nielsen, J. Eric; Pawson, Steven; Stolarski, Richard S.

    2007-01-01

    The Antarctic ozone hole develops each year and culminates by early spring (late September - early October). The severity of the hole has been assessed from satellites using the minimum total ozone value from the October monthly mean (depth of the hole) and by calculating the average area coverage during this September-October period. Profile information shows that ozone is completely destroyed in the 14-21 km layer by early October. Ozone is mainly destroyed by halogen (chlorine and bromine) catalytic cycles, and these losses are modulated by temperature variations. Because atmospheric halogen levels are responding to international agreements that limit or phase out production, the amount of halogens in the stratosphere should decrease over the next few decades. Using projections of halogen levels combined with age-of-air estimates, we find that the ozone hole is recovering at an extremely slow rate and that large ozone holes will regularly recur over the next 2 decades. We estimate that the ozone hole will begin to show first signs of size decrease in about 2023, and the hole will fully recover to pre-1980 levels in approximately 2070. Estimates of the ozone hole's recovery from models reveal important differences that will be discussed.

  10. Indoor/outdoor concentrations of ozone and peroxyacetyl nitrate (PAN).

    PubMed

    Jakobi, G; Fabian, P

    1997-05-01

    Photochemical pollutants such as ozone and peroxyacetyl nitrate (PAN) could adversely affect human health, especially with relation to effects on lung function. For a realistic assessment of ambient concentrations, both outdoor and indoor measurements of ozone and PAN are required, because people stay indoors for most of the time. Indoor/outdoor concentration ratios, indoor half-life times and indoor chemistry including physicochemical reactions on surfaces are quite well known for ozone, but not for PAN. While ozone is removed very rapidly mainly by heterogeneous reactions on surfaces or by gasphase reactions with e.g. carpet emissions, no such processes are known for PAN at present. The main removal process for PAN is thermal decay. Indoor concentrations of ozone and PAN can be a significant fraction of those outdoors highly depending on the ventilation pattern. Our measurements in various kinds of non-air-conditioned rooms show maximal indoor concentrations between 80 and 100% of those outdoors for ozone and PAN, respectively. Average indoor/outdoor ratios were calculated of 0.5 for ozone and between 0.7 and 0.9 for PAN. The half-life times ranged between only a few minutes for ozone and 0.5 to 1 h for PAN.

  11. Who is more affected by ozone pollution? A systematic review and meta-analysis.

    PubMed

    Bell, Michelle L; Zanobetti, Antonella; Dominici, Francesca

    2014-07-01

    Ozone is associated with adverse health; however, less is known about vulnerable/sensitive populations, which we refer to as sensitive populations. We systematically reviewed epidemiologic evidence (1988-2013) regarding sensitivity to mortality or hospital admission from short-term ozone exposure. We performed meta-analysis for overall associations by age and sex; assessed publication bias; and qualitatively assessed sensitivity to socioeconomic indicators, race/ethnicity, and air conditioning. The search identified 2,091 unique papers, with 167 meeting inclusion criteria (73 on mortality and 96 on hospitalizations and emergency department visits, including 2 examining both mortality and hospitalizations). The strongest evidence for ozone sensitivity was for age. Per 10-parts per billion increase in daily 8-hour ozone concentration, mortality risk for younger persons, at 0.60% (95% confidence interval (CI): 0.40, 0.80), was statistically lower than that for older persons, at 1.27% (95% CI: 0.76, 1.78). Findings adjusted for publication bias were similar. Limited/suggestive evidence was found for higher associations among women; mortality risks were 0.39% (95% CI: -0.22, 1.00) higher than those for men. We identified strong evidence for higher associations with unemployment or lower occupational status and weak evidence of sensitivity for racial/ethnic minorities and persons with low education, in poverty, or without central air conditioning. Findings show that some populations, especially the elderly, are particularly sensitive to short-term ozone exposure. PMID:24872350

  12. Stratospheric ozone depletion.

    PubMed

    Rowland, F Sherwood

    2006-05-29

    Solar ultraviolet radiation creates an ozone layer in the atmosphere which in turn completely absorbs the most energetic fraction of this radiation. This process both warms the air, creating the stratosphere between 15 and 50 km altitude, and protects the biological activities at the Earth's surface from this damaging radiation. In the last half-century, the chemical mechanisms operating within the ozone layer have been shown to include very efficient catalytic chain reactions involving the chemical species HO, HO2, NO, NO2, Cl and ClO. The NOX and ClOX chains involve the emission at Earth's surface of stable molecules in very low concentration (N2O, CCl2F2, CCl3F, etc.) which wander in the atmosphere for as long as a century before absorbing ultraviolet radiation and decomposing to create NO and Cl in the middle of the stratospheric ozone layer. The growing emissions of synthetic chlorofluorocarbon molecules cause a significant diminution in the ozone content of the stratosphere, with the result that more solar ultraviolet-B radiation (290-320 nm wavelength) reaches the surface. This ozone loss occurs in the temperate zone latitudes in all seasons, and especially drastically since the early 1980s in the south polar springtime-the 'Antarctic ozone hole'. The chemical reactions causing this ozone depletion are primarily based on atomic Cl and ClO, the product of its reaction with ozone. The further manufacture of chlorofluorocarbons has been banned by the 1992 revisions of the 1987 Montreal Protocol of the United Nations. Atmospheric measurements have confirmed that the Protocol has been very successful in reducing further emissions of these molecules. Recovery of the stratosphere to the ozone conditions of the 1950s will occur slowly over the rest of the twenty-first century because of the long lifetime of the precursor molecules.

  13. Stratospheric ozone depletion

    PubMed Central

    Rowland, F. Sherwood

    2006-01-01

    Solar ultraviolet radiation creates an ozone layer in the atmosphere which in turn completely absorbs the most energetic fraction of this radiation. This process both warms the air, creating the stratosphere between 15 and 50 km altitude, and protects the biological activities at the Earth's surface from this damaging radiation. In the last half-century, the chemical mechanisms operating within the ozone layer have been shown to include very efficient catalytic chain reactions involving the chemical species HO, HO2, NO, NO2, Cl and ClO. The NOX and ClOX chains involve the emission at Earth's surface of stable molecules in very low concentration (N2O, CCl2F2, CCl3F, etc.) which wander in the atmosphere for as long as a century before absorbing ultraviolet radiation and decomposing to create NO and Cl in the middle of the stratospheric ozone layer. The growing emissions of synthetic chlorofluorocarbon molecules cause a significant diminution in the ozone content of the stratosphere, with the result that more solar ultraviolet-B radiation (290–320 nm wavelength) reaches the surface. This ozone loss occurs in the temperate zone latitudes in all seasons, and especially drastically since the early 1980s in the south polar springtime—the ‘Antarctic ozone hole’. The chemical reactions causing this ozone depletion are primarily based on atomic Cl and ClO, the product of its reaction with ozone. The further manufacture of chlorofluorocarbons has been banned by the 1992 revisions of the 1987 Montreal Protocol of the United Nations. Atmospheric measurements have confirmed that the Protocol has been very successful in reducing further emissions of these molecules. Recovery of the stratosphere to the ozone conditions of the 1950s will occur slowly over the rest of the twenty-first century because of the long lifetime of the precursor molecules. PMID:16627294

  14. Stratospheric ozone depletion.

    PubMed

    Rowland, F Sherwood

    2006-05-29

    Solar ultraviolet radiation creates an ozone layer in the atmosphere which in turn completely absorbs the most energetic fraction of this radiation. This process both warms the air, creating the stratosphere between 15 and 50 km altitude, and protects the biological activities at the Earth's surface from this damaging radiation. In the last half-century, the chemical mechanisms operating within the ozone layer have been shown to include very efficient catalytic chain reactions involving the chemical species HO, HO2, NO, NO2, Cl and ClO. The NOX and ClOX chains involve the emission at Earth's surface of stable molecules in very low concentration (N2O, CCl2F2, CCl3F, etc.) which wander in the atmosphere for as long as a century before absorbing ultraviolet radiation and decomposing to create NO and Cl in the middle of the stratospheric ozone layer. The growing emissions of synthetic chlorofluorocarbon molecules cause a significant diminution in the ozone content of the stratosphere, with the result that more solar ultraviolet-B radiation (290-320 nm wavelength) reaches the surface. This ozone loss occurs in the temperate zone latitudes in all seasons, and especially drastically since the early 1980s in the south polar springtime-the 'Antarctic ozone hole'. The chemical reactions causing this ozone depletion are primarily based on atomic Cl and ClO, the product of its reaction with ozone. The further manufacture of chlorofluorocarbons has been banned by the 1992 revisions of the 1987 Montreal Protocol of the United Nations. Atmospheric measurements have confirmed that the Protocol has been very successful in reducing further emissions of these molecules. Recovery of the stratosphere to the ozone conditions of the 1950s will occur slowly over the rest of the twenty-first century because of the long lifetime of the precursor molecules. PMID:16627294

  15. [Influence of ozone on snap bean under ambient air in two sites of northern China].

    PubMed

    Yuan, Xiang-Yang; Zhang, Wei-Wei; Sun, Jing-Song; Hu, En-Zhu; Zhang, Yu-Long; Zhang, Hong-Xing; Tian, Yuan; Feng, Zhao-Zhong

    2014-08-01

    Tropospheric ozone (O3) has been assumed the most phytotoxic air pollutant and the snap bean (Phaseolus vulgaris L.) is known to be an ozone-sensitive species. Two genotypes (R123, ozone-tolerance, S156, ozone-sensitivity) of snap bean were explored in three places. The objective of this study was to evaluate whether the snap bean was influenced under the current ambient ozone concentration. The findings indicated that the leaves of bean grown at Research Center for Eco-Environmental Sciences (RCEES), Chinese Academy of Sciences and ChangPing showed visible ozone symptoms under the ambient ozone concentration, and the averaged ozone injury proportion in S156 was 23.5% higher than R123 during the entire growth season. The ozone damage to the snap bean depends on the plant growing stages. The injury symptoms appeared just after flowering, increased from the stages of flowering to pod formation, and reached the maximum at the stages of pod maturation. The ratio of S156/R123 in pod yield was 0.48, and 0.24 and 0.73 in the RCEES, ChangPing and Harbin, respectively. The ratio close to 1 was assumed that the plant growth is not affected by ozone, and the lower ratio is, the more damage caused by ozone. Obviously, the current ambient ozone concentration of Beijing area has significantly caused the yield loss of snap bean.

  16. Ozone - plant surface reactions an important ozone loss term?

    NASA Astrophysics Data System (ADS)

    Hansel, Armin; Jud, Werner; Fischer, Lukas; Canaval, Eva; Wohlfahrt, Georg; Tissier, Alain

    2015-04-01

    Elevated tropospheric ozone concentrations are considered a toxic threat to plants responsible for global crop losses with associated economic costs of several billions dollar per year. Plant injuries have been related to the uptake of ozone through stomatal pores and oxidative effects damaging the internal leaf tissue. But a striking question remains: How much ozone enters the plant through open stomata and how much ozone is lost by chemical reactions at the plant surface? Until now surface losses are estimated from measured total ozone deposition fluxes and calculated stomatal conductance values. While stomatal conductance of CO2 and H2O is well understood and extensively used in describing plant atmosphere gas exchange, stomatal conductance of ozone is not well known. Here we use different Nicotiana tabacum varieties and find that surface reactions of ozone with diterpenoids synthesized by glandular trichomes reduce ozone flux through open stomata. Our measurements reveal that fast ozone loss at the plant surface is accompanied with prompt release of oxygenated volatile compounds. In the ozone fumigation experiments of different Nicotiana tabacum varieties the release of specific volatile oxy-VOCs allowed to identify the semi volatile precursor compounds at the plant surface. Ozone fumigation experiments with Norway spruce (Picea abies) and Scots Pine (Pinus sylvestris), two common species in the Northern Hemisphere, show also a significant ozone loss at the plant surface for Picea abies. Fluid dynamic calculations of ozone transport in the diffusive leaf boundary layer reveal a vertical but no horizontal ozone gradient thus reducing ozone fluxes through the pores in case of efficient ozone scavenging plant surfaces. We explain this efficient ozone protection mechanism by the porous surface architecture of plants in combination with unsaturated semi-volatile compounds deposited at the plant surface. These results show that unsaturated semi-volatile compounds at

  17. Ozone Profiles and Tropospheric Ozone from Global Ozone Monitoring Experiment

    NASA Technical Reports Server (NTRS)

    Liu, X.; Chance, K.; Sioris, C. E.; Sparr, R. J. D.; Kuregm, T. P.; Martin, R. V.; Newchurch, M. J.; Bhartia, P. K.

    2003-01-01

    Ozone profiles are derived from backscattered radiances in the ultraviolet spectra (290-340 nm) measured by the nadir-viewing Global Ozone Monitoring Experiment using optimal estimation. Tropospheric O3 is directly retrieved with the tropopause as one of the retrieval levels. To optimize the retrieval and improve the fitting precision needed for tropospheric O3, we perform extensive wavelength and radiometric calibrations and improve forward model inputs. Retrieved O3 profiles and tropospheric O3 agree well with coincident ozonesonde measurements, and the integrated total O3 agrees very well with Earth Probe TOMS and Dobson/Brewer total O3. The global distribution of tropospheric O3 clearly shows the influences of biomass burning, convection, and air pollution, and is generally consistent with our current understanding.

  18. Antarctic Ozone loss 1988-2008 history at Dumont d

    NASA Astrophysics Data System (ADS)

    Kuttippurath, J.; Goutail, F.; Pommereau, J. P.; Pazmino, A.; Feng, W.; Chipperfield, M.

    2009-04-01

    Even if the saturation of Antarctic ozone loss is almost achieved, the time of ozone recovery to pre-industrial level is still uncertain. In order to make amendments in international treaties aimed at controlling ozone depleting substances (ODS), the long term monitoring of ozone level by independent and complementary space borne and ground-based observations is mandatory. The consistency between the two approaches and model simulations is being investigated by comparison of ozone depleted amounts derived every year since 1988 by the transport method above the French NDACC station of Dumont d'Urville from the measurements of the G-B SAOZ UV-Vis and the series of TOMS-Nimbus, -Meteor, -Earth Probe and OMI, and simulations by the SLIMCAT 3D CTM. The loss derived from SAOZ is 5% larger than that shown by TOMS, whereas the difference vanishes in 2006 and 2007 with OMI. The cumulative depletion in the vortex estimated from a ten-day average of ozone loss at 475 K during the winter is 55% on average. The strongest depletion is occurred in 1994, 1995, 1997 and 2006 exceeding 60%, whereas the lowest of less than 50% is observed in 1988, 1992, 2002, 2005 and 2007. There is indication of an increasing trend in the ozone loss in 1988-1994 related to the increase in ODS, followed by a level off or a small decreasing trend since 1996.

  19. Which metric of ambient ozone to predict daily mortality?

    NASA Astrophysics Data System (ADS)

    Moshammer, Hanns; Hutter, Hans-Peter; Kundi, Michael

    2013-02-01

    It is well known that ozone concentration is associated with daily cause specific mortality. But which ozone metric is the best predictor of the daily variability in mortality? We performed a time series analysis on daily deaths (all causes, respiratory and cardiovascular causes as well as death in elderly 65+) in Vienna for the years 1991-2009. We controlled for seasonal and long term trend, day of the week, temperature and humidity using the same basic model for all pollutant metrics. We found model fit was best for same day variability of ozone concentration (calculated as the difference between daily hourly maximum and minimum) and hourly maximum. Of these the variability displayed a more linear dose-response function. Maximum 8 h moving average and daily mean value performed not so well. Nitrogen dioxide (daily mean) in comparison performed better when previous day values were assessed. Same day ozone and previous day nitrogen dioxide effect estimates did not confound each other. Variability in daily ozone levels or peak ozone levels seem to be a better proxy of a complex reactive secondary pollutant mixture than daily average ozone levels in the Middle European setting. If this finding is confirmed this would have implications for the setting of legally binding limit values.

  20. [Effects of synoptic type on surface ozone pollution in Beijing].

    PubMed

    Tang, Gui-qian; Li, Xin; Wang, Xiao-ke; Xin, Jin-yuan; Hu, Bo; Wang, Li-li; Ren, Yu-fen; Wang, Yue-Si

    2010-03-01

    Ozone (O), influenced by meteorological factors, is a primary gaseous photochemical pollutant during summer to fall in Beijing' s urban ambient. Continuous monitoring during July to September in 2008 was carried out at four sites in Beijing. Analyzed with synoptic type, the results show that the ratios of pre-low cylonic (mainly Mongolia cyclone) and pre-high anticylonic to total weather conditions are about 42% and 20%, illustrating the high-and low-ozone episodes, respectively. At the pre-low cylonic conditions, high temperature, low humidity, mountain and valley winds caused by local circulation induce average hourly maximum ozone concentration (volume fraction) up to 102.2 x 10(-9), negative correlated with atmospheric pressure with a slope of -3.4 x 10(-9) Pa(-1). The time of mountain wind changed to valley wind dominates the diurnal time of maximum ozone, generally around 14:00. At the pre-high anticylonic conditions, low temperature, high humidity and systematic north wind induce average hourly maximum ozone concentration (volume fraction) only 49.3 x 10(-9), the diurnal time of maximum ozone is deferred by continuous north wind till about 16:00. The consistency of photochemical pollution in Beijing region shows that good correlation exists between synoptic type and ozone concentration. Therefore, getting an eye on the structure and evolution of synoptic type is of great significances for forecasting the photochemical pollution.

  1. Ozone Photolysis: Strong Isotopologue/isotopomer Selectivity in the Stratosphere

    NASA Astrophysics Data System (ADS)

    Gatti, Fabien; Ndengue, Steve; Jost, Remy; Halasz, Gabor; Vibok, Agnes

    2013-06-01

    Using the visible-UV absorption cross section (Abs. XS) of five ozone isotopologues and an averaged actinic flux, we have calculated the contribution of the atmospheric ozone photolysis to the oxygen isotope and ozone isotopologue/isotopomer enrichment. Five ozone isotopologues/isotopomers are considered among which three are symmetric, O^{16}3 (noted 666), O^{16}O^{17}O^{16} (676) and O^{16}O^{18}O^{16} (686), and two are asymmetric, O^{17}O^{16}_2 (667) and O^{18}O^{16}_2 (668). The photolysis rates of the five ozone isotopologues have been calculated as a function of altitude. The Multi Configuration Time Dependent Hartree (MCTDH) method and the potential energy surfaces calculates by R. Schinke and coworkers have been used. We have used experimental actinic fluxes, averaged for latitude and season, for altitudes varying by step of 4km up to 80km. Below 35km, the contribution of the Hartley band to the photolysis rates is restricted to its low energy range, named the Huggins band, which has strong isotopologue/isotopomer selectivity and then induces strong enrichment. Consequently, the isotopologue enrichment's due to ozone photolysis are strongly dependent of the altitude, with pronounced enrichment peaks around 35 km, the altitude corresponding to the maximum relative contribution of the Huggins band. We will also present some new simulations for the simulation of laser-induced quantum dynamics of the electronic and nuclear motion in the ozone molecule on the attosecond time scale.

  2. Polar Ozone Losses

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.; Bhartia, P. K. (Technical Monitor)

    2001-01-01

    Since the discovery of the Antarctic ozone hole, a great deal of attention has been focused on the polar regions to both identify the chemistry and physics of the large losses, and to provide an understanding of the future of polar ozone. In this review talk, I will discuss the secular trends of ozone in both the Antarctic and Arctic regions, and I will review some of the principal research results of the last few years. In particular, I will emphasize some of the results from the SOLVE-THESEO 2000 campaign that occurred over the course of the winter of 1999-2000.

  3. Arctic ozone loss

    SciTech Connect

    Zurer, P.S.

    1989-03-06

    Scientists have returned from the first comprehensive probe of the Arctic stratosphere with unexpectedly dire results: The winter atmosphere in the north polar region is loaded with the same destructive chlorine compounds that cause the Antarctic ozone hole. Atmospheric researchers who only a few weeks ago were comforted by the thought that the warmer Northern Hemisphere is strongly protected from the processes that lead to massive losses of ozone during spring in Antarctica now see very little standing in the way of an Arctic ozone hole.

  4. Short-term effects of multiple ozone metrics on daily mortality in a megacity of China.

    PubMed

    Li, Tiantian; Yan, Meilin; Ma, Wenjun; Ban, Jie; Liu, Tao; Lin, Hualiang; Liu, Zhaorong

    2015-06-01

    Epidemiological studies have widely demonstrated association between ambient ozone and mortality, though controversy remains, and most of them only use a certain metric to assess ozone levels. However, in China, few studies have investigated the acute effects of ambient ozone, and rare studies have compared health effects of multiple daily metrics of ozone. The present analysis aimed to explore variability of estimated health effects by using multiple temporal ozone metrics. Six metrics of ozone, 1-h maximum, maximum 8-h average, 24-h average, daytime average, nighttime average, and commute average, were used in a time-series study to investigate acute mortality associated with ambient ozone pollution in Guangzhou, China, using 3 years of daily data (2006-2008). We used generalized linear models with Poisson regression incorporating natural spline functions to analyze the mortality, ozone, and covariate data. We also examined the association by season. Daily 1- and 8-h maximum, 24-h average, and daytime average concentrations yielded statistically significant associations with mortality. An interquartile range (IQR) of O3 metric increase of each ozone metric (lag 2) corresponds to 2.92 % (95 % confidence interval (CI) 0.24 to 5.66), 3.60 % (95 % CI, 0.92 to 8.49), 3.03 % (95 % CI, 0.57 to 15.8), and 3.31 % (95 % CI, 0.69 to 10.4) increase in daily non-accidental mortality, respectively. Nighttime and commute metrics were weakly associated with increased mortality rate. The associations between ozone and mortality appeared to be more evident during cool season than in the warm season. Results were robust to adjustment for co-pollutants, weather, and time trend. In conclusion, these results indicated that ozone, as a widespread pollutant, adversely affects mortality in Guangzhou.

  5. Lidar-derived Correlations Between Lower-tropospheric Column and Surface Ozone: Implications for Satellite Observations

    NASA Astrophysics Data System (ADS)

    Senff, C. J.; Langford, A. O.; Alvarez, R. J. _II, II; Kirgis, G.; Choukulkar, A.; Brewer, A.; Banta, R. M.; Weickmann, A. M.; Sandberg, S.; Olson, E.

    2015-12-01

    One of the data products that will be provided by the TEMPO satellite mission is 0-2 km ozone column concentration. To make inferences about surface air quality from this data product, the relationship between lower-tropospheric column and surface ozone concentrations and their diurnal, seasonal, and spatial variations have to be well understood. To characterize these relationships, we have used ozone profile observations obtained with NOAA's truck-based, scanning TOPAZ ozone lidar from several recent field campaigns including Discover-AQ Houston and Colorado, the Uintah Basin Wintertime Ozone Study (UBWOS), and the Las Vegas Ozone Study (LVOS). The TOPAZ lidar is ideally suited for this kind of study because it provides ozone profiles from about 15 m above ground level (AGL) up to 3 km AGL at high spatial and temporal resolution. We have used the lidar observations closest to the ground as a proxy for surface ozone and compared them to the 0-2 km AGL average column ozone concentrations measured with the lidar. Results from the Discover-AQ Colorado campaign show that in the afternoon, when the boundary layer (BL) was deep and well mixed, ozone column and surface concentrations agreed quite well. However, during the morning hours, ozone column concentrations were significantly higher than those at the surface, because ozone was depleted in a shallow surface layer due to titration and deposition, whereas ozone levels in the residual layer aloft remained moderately high. The analysis of column and surface ozone correlations using ozone lidar observations from the Discover-AQ Houston, UBWOS and LVOS campaigns is currently underway. The results from these studies will provide additional insights into the relationship between column and surface ozone, in particular their variation as a function of measurement location and season, and their dependence on BL processes such as mixed layer height evolution, land-sea breeze circulation, and terrain-induced flows.

  6. ROCOZ-A ozone measurements during the Stratospheric Ozone Intercomparison Campaign (STOIC)

    NASA Astrophysics Data System (ADS)

    Barnes, Robert A.; Parsons, Chester L.; Grothouse, Arthur P.

    1995-05-01

    We present a set of ROCOZ-A (rocket ozonesonde) ozone measurements during the October/November 1988 (pre-STOIC) and the July/August 1989 Stratospheric Ozone Intercomparison Campaign (STOIC) in southern California. ROCOZ-A and its associated electrochemical concentration cell (ECC) ozonesondes participated in the comparisons as established techniques for the validation of lidar and microwave instruments that have been proposed for the Network for the Detection of Stratospheric Change (NDSC). For the proposed network instruments, STOIC has provided a picture of their performance characteristics in 1989 and has given an estimate of their future performance in the NDSC. For ROCOZ-A, STOIC has added new information on its accuracy and precision. It is this continuing characterization that gives ROCOZ-A its value in comparisons. The STOIC comparisons show a shift of 5-6% in ROCOZ-A ozone densities (ROCOZ-A higher) from October/November 1988 to July/August 1989. This shift has been seen in comparisons with the Stratospheric Aerosol and Gas Experiment II (SAGE II), ECC ozonesondes, and the Jet Propulsion Laboratory (JPL) lidar. The source of this shift has not been determined. Until this new error source is resolved, we recommend that the previously quoted accuracy estimate for ROCOZ-A ozone measurements be increased from 5-7% to 8-10%. About 2% of the difference between ROCOZ-A ozone measurements and those from the proposed network instruments in 1989 appears to be due to differences in atmospheric ozone between the two STOIC sites. A correction for these site-to-site differences brings the ROCOZ-A ozone measurements within 10% of all of the other STOIC instruments, and the average agreement (ROCOZ-A 6% higher) becomes consistent with the historical set of ROCOZ-A comparisons. The STOIC comparisons have shown structures in stratospheric ozone that cannot be resolved by ROCOZ-A with its 4-km vertical resolution. In addition, comparisons with nighttime measurements from the

  7. Energetic particle precipitation: A major driver of the ozone budget in the Antarctic upper stratosphere

    NASA Astrophysics Data System (ADS)

    Damiani, Alessandro; Funke, Bernd; Santee, Michelle L.; Cordero, Raul R.; Watanabe, Shingo

    2016-04-01

    Geomagnetic activity is thought to affect ozone and, possibly, climate in polar regions via energetic particle precipitation (EPP) but observational evidence of its importance in the seasonal stratospheric ozone variation on long time scales is still lacking. Here we fill this gap by showing that at high southern latitudes, late winter ozone series, covering the 1979-2014 period, exhibit an average stratospheric depletion of about 10-15% on a monthly basis caused by EPP. Daily observations indicate that every austral winter EPP-induced low ozone concentrations appear at about 45 km in late June and descend later to 30 km, before disappearing by September. Such stratospheric variations are coupled with mesospheric ozone changes also driven by EPP. No significant correlation between these ozone variations and solar ultraviolet irradiance has been found. This suggests the need of including the EPP forcing in both ozone model simulations and trend analysis.

  8. Ozone Correlative Measurements Workshop

    NASA Technical Reports Server (NTRS)

    Hilsenrath, E. (Editor)

    1985-01-01

    A study was conducted to determine the necessary parameters for the correlation of data on Earth ozone. Topics considered were: (1) measurement accuracy; (2) equipment considerations (SBUV); and (3) ground based measurements to support satellite data.

  9. Ozone Therapy in Dentistry

    PubMed Central

    Domb, William C

    2014-01-01

    Summary The 21st century dental practice is quite dynamic. New treatment protocols and new materials are being developed at a rapid pace. Ozone dental therapy falls into the category of new treatment protocols in dentistry, yet ozone is not new at all. Ozone therapy is already a major treatment modality in Europe, South America and a number of other countries. What is provided here will not be an exhaustive scientific treatise so much as a brief general introduction into what dentists are now doing with ozone therapies and the numerous oral/systemic links that make this subject so important for physicians so that, ultimately, they may serve their patients more effectively and productively. PMID:25363268

  10. 40 CFR Appendix P to Part 50 - Interpretation of the Primary and Secondary National Ambient Air Quality Standards for Ozone

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... for each calendar day during the O3 monitoring season. The daily maximum 8-hour concentration for a...% of the days within the O3 monitoring season, on average, for the 3-year period, with a minimum data completeness requirement in any one year of at least 75% of the days within the O3 monitoring season....

  11. 40 CFR Appendix P to Part 50 - Interpretation of the Primary and Secondary National Ambient Air Quality Standards for Ozone

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... for each calendar day during the O3 monitoring season. The daily maximum 8-hour concentration for a...% of the days within the O3 monitoring season, on average, for the 3-year period, with a minimum data completeness requirement in any one year of at least 75% of the days within the O3 monitoring season....

  12. 78 FR 25236 - Approval and Promulgation of Implementation Plans; New York; Infrastructure SIP for the 1997 8...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-04-30

    ... information? On July 18, 1997, EPA promulgated new and revised NAAQS for 8-hour ozone (62 FR 38856) and PM 2.5 (62 FR 38652). The ozone NAAQS is based on 8-hour average concentrations. The 8-hour averaging period.... EPA strengthened the 24-hour PM 2.5 NAAQS from 65 g/m\\3\\ to 35 g/m\\3\\ on October 17, 2006 (71 FR...

  13. The ozone backlash

    SciTech Connect

    Taubes, G.

    1993-06-11

    While evidence for the role of chlorofluorocarbons in ozone depletion grows stronger, researchers have recently been subjected to vocal public criticism of their theories-and their motives. Their understanding of the mechanisms of ozone destruction-especially the annual ozone hole that appears in the Antarctic-has grown stronger, yet everywhere they go these days, they seem to be confronted by critics attacking their theories as baseless. For instance, Rush Limbaugh, the conservative political talk-show host and now-best-selling author of The Way Things Ought to Be, regularly insists that the theory of ozone depletion by CFCs is a hoax: bladerdash and poppycock. Zoologist Dixy Lee Ray, former governor of the state of Washington and former head of the Atomic Energy Commission, makes the same argument in her book, Trashing the Planet. The Wall Street Journal and National Review have run commentaries by S. Fred Singer, a former chief scientists for the Department of Transportation, purporting to shoot holes in the theory of ozone depletion. Even the June issue of Omni, a magazine with a circulation of more than 1 million that publishes a mixture of science and science fiction, printed a feature article claiming to expose ozone research as a politically motivated scam.

  14. Americans' Average Radiation Exposure

    SciTech Connect

    NA

    2000-08-11

    We live with radiation every day. We receive radiation exposures from cosmic rays, from outer space, from radon gas, and from other naturally radioactive elements in the earth. This is called natural background radiation. It includes the radiation we get from plants, animals, and from our own bodies. We also are exposed to man-made sources of radiation, including medical and dental treatments, television sets and emission from coal-fired power plants. Generally, radiation exposures from man-made sources are only a fraction of those received from natural sources. One exception is high exposures used by doctors to treat cancer patients. Each year in the United States, the average dose to people from natural and man-made radiation sources is about 360 millirem. A millirem is an extremely tiny amount of energy absorbed by tissues in the body.

  15. Background ozone over the United States in summer: Origin, trend, and contribution to pollution episodes

    NASA Astrophysics Data System (ADS)

    Fiore, Arlene M.; Jacob, Daniel J.; Bey, Isabelle; Yantosca, Robert M.; Field, Brendan D.; Fusco, Andrew C.; Wilkinson, James G.

    2002-08-01

    Observations indicate that ozone (O3) concentrations in surface air over the United States in summer contain a 20-45 ppbv background contribution, presumably reflecting transport from outside the North American boundary layer. We use a three-dimensional global model of tropospheric chemistry driven by assimilated meteorological observations to investigate the origin of this background and to quantify its contribution to total surface O3 on both average and highly polluted summer days. The model simulation is evaluated with a suite of surface and aircraft observations over the United States from the summer of 1995. The model reproduces the principal features in the observed distributions of O3 and its precursors, including frequency distributions of O3 concentrations and the development of regional high-O3 episodes in the eastern United States. Comparison of simulations with 1995 versus 1980 global fossil fuel emissions indicates that the model captures the previously observed decrease in the high end of the O3 probability distribution in surface air over the United States (reflecting reduction of domestic hydrocarbon emissions) and the increase in the low end (reflecting, at least in the model, rising Asian emissions). In the model, background O3 produced outside of the North American boundary layer contributes an average 25-35 ppbv to afternoon O3 concentrations in surface air in the western United States. and 15-30 ppbv in the eastern United States during the summer of 1995. This background generally decays to below 15 ppbv during the stagnation conditions conducive to exceedances of the 8-hour 0.08 ppmv (80 ppbv) National Ambient Air Quality Standard (NAAQS) for O3. A high background contribution of 25-40 ppbv is found during 9% of these exceedances, reflecting convective mixing of free tropospheric O3 from aloft, followed by rapid production within the U.S. boundary layer. Anthropogenic emissions in Asia and Europe are found to increase afternoon O3

  16. Changes in the frequency and return level of high ozone pollution events over the eastern United States following emission controls

    NASA Astrophysics Data System (ADS)

    Rieder, H. E.; Fiore, A. M.; Polvani, L. M.; Lamarque, J.-F.; Fang, Y.

    2013-03-01

    In order to quantify the impact of recent efforts to abate surface ozone (O3) pollution, we analyze changes in the frequency and return level of summertime (JJA) high surface O3 events over the eastern United States (US) from 1988-1998 to 1999-2009. We apply methods from extreme value theory (EVT) to maximum daily 8-hour average ozone (MDA8 O3) observed by the Clean Air Status and Trends Network (CASTNet) and define O3 extremes as days on which MDA8 O3 exceeds a threshold of 75 ppb (MDA8 O3>75). Over the eastern US, we find that the number of summer days with MDA8 O3>75 declined on average by about a factor of two from 1988-1998 to 1999-2009. The applied generalized Pareto distribution (GPD) fits the high tail of MDA8 O3 much better than a Gaussian distribution and enables the derivation of probabilistic return levels (describing the probability of exceeding a value x within a time window T) for high O3 pollution events. This new approach confirms the significant decline in both frequency and magnitude of high O3 pollution events over the eastern US during recent years reported in prior studies. Our analysis of 1-yr and 5-yr return levels at each station demonstrates the strong impact of changes in air quality regulations and subsequent control measures (e.g., the ‘NOx SIP Call’), as the 5-yr return levels of the period 1999-2009 correspond roughly to the 1-yr return levels of the earlier time period (1988-1998). Regionally, the return levels dropped between 1988-1998 and 1999-2009 by about 8 ppb in the Mid-Atlantic (MA) and Great Lakes (GL) regions, while the strongest decline, about 13 ppb, is observed in the Northeast (NE) region. Nearly all stations (21 out of 23) have 1-yr return levels well below 100 ppb and 5-yr return levels well below 110 ppb in 1999-2009. Decreases in eastern US O3 pollution are largest after full implementation of the nitrogen oxide (NOx) reductions under the ‘NOx SIP Call’. We conclude that the application of EVT methods

  17. Long-term ozone and temperature correlations above SANAE, Antarctica

    NASA Technical Reports Server (NTRS)

    Bodeker, Gregory E.; Scourfield, Malcolm W. J.

    1994-01-01

    A significant decline in Antarctic total column ozone and upper air temperatures has been observed in recent years. Furthermore, high correlations between monthly mean values of ozone and stratospheric temperature have been measured above Syowa, Antarctica. For the observations reported here, data from TOMS (Total Ozone Mapping Spectrometer) aboard the Nimbus 7 satellite have been used to examine the 1980 to 1990 decrease in total column ozone above the South African Antarctic base of SANAE (70 deg 18 min S, 2 deg 21 min W). The cooling of the Antarctic stratosphere above SANAE during this period has been investigated by examining upper air temperatures at the 150, 100, 70, 50, and 30 hPa levels obtained from daily radiosonde balloon launches. Furthermore, these two data sets have been used to examine long-term, medium-term, and short-term correlations between total column ozone and the temperatures at each of the five levels. The trend in SANAE total column ozone has been found to be -4.9 DU/year, while upper air temperatures have been found to decrease at around 0.3 C/year. An analysis of monthly average SANAE total column ozone has shown the decrease to be most severe during the month of September with a trend of -7.7 DU/year. A strong correlation (r(exp 2) = 0.92) has been found between yearly average total column ozone and temperature at the 100 hPa level. Daily ozone and temperature correlations show high values from September to November, at a time when the polar vortex is breaking down.

  18. Ozone in the Pacific Troposphere from Ozonesonde Observations

    NASA Technical Reports Server (NTRS)

    Oltmans, S. J.; Johnson, B. J.; Harris, J. M.; Voemel, H.; Koshy, K.; Simon, P.; Bendura, R.; Thompson, A. M.; Logan, J. A.; Hasebe, F.; Einaudi, Franco (Technical Monitor)

    2000-01-01

    Ozone vertical profile measurements obtained from ozonesondes flown at Fiji, Samoa, Tahiti and the Galapagos are used to characterize ozone in the troposphere over the tropical Pacific. There is a significant seasonal variation at each of these sites. At sites in both the eastern and western Pacific, ozone is highest at almost all levels in the troposphere during the September-November season and lowest during, March-May. There is a relative maximum at all of the sites in the mid-troposphere during all seasons of the year (the largest amounts are usually found near the tropopause). This maximum is particularly pronounced during, the September-November season. On average, throughout the troposphere at all seasons, the Galapagos has larger ozone amounts than the western Pacific sites. A trajectory climatology is used to identify the major flow regimes that are associated with the characteristic ozone behavior at various altitudes and seasons. The enhanced ozone seen in the mid-troposphere during September-November is associated with flow from the continents. In the western Pacific this flow is usually from southern Africa (although 10-day trajectories do not always reach the continent), but also may come from Australia and Indonesia. In the Galapagos the ozone peak in the mid-troposphere is seen in flow from the South American continent and particularly from northern Brazil. The time of year and flow characteristics associated with the ozone mixing ratio peaks seen in both the western and eastern Pacific suggest that these enhanced ozone values result from biomass burning. In the upper troposphere low ozone amounts are seen with flow that originates in the convective western Pacific.

  19. A passive ozone sampler based on a reaction with iodide.

    PubMed

    Yanagisawa, Y

    1994-02-01

    A new passive sampler for ozone and its simple analytical system have been developed. Because it is small and sensitive, the sampler can be used for determining personal exposures to ozone and oxidants and for multilocation measurements. The sampler consists of an electrode, a spacer, and several layers of membrane filters and Teflon meshes. The electrode is a carbon paper disk coated with nylon-6 polymer and potassium iodide. The membrane filters are used to remove interferences. A sampling rate of ozone is controlled by the spacer and Teflon meshes. Iodine is liberated by an oxidation reaction of potassium iodide with ozone. The iodine is stabilized by forming a charge transfer complex with nylon-6 and is accumulated in the nylon-6 layer. The amount of iodine, which is proportional to the level of ozone exposure, is quantified by constant current coulometry. The discharge time of a galvanic battery is measured using the electrode as a positive electrode and a zinc plate as a counter electrode. A time-weighted average concentration of ozone is derived from the discharge time after exposing the electrode to ozone. The effects of various environmental conditions on the sampler's performance were investigated. The results indicated that the sampler showed a linear response to ozone exposure up to 1,450 parts per billion for every hour of use (ppb.hour). The minimum detectable exposure was about 400 ppb.hour. The effects of surface wind velocity, temperature, and humidity were small. However, a relative humidity below 20% resulted in an underestimation of the ozone concentration. Because the electrode requires no pretreatment and the analytical method is very simple, this method is suitable for large-scale studies of personal exposures to ozone and oxidants using multilocation measurements.

  20. Ozone-vegetation interaction in the Earth system: implications for air quality, ecosystems and agriculture

    NASA Astrophysics Data System (ADS)

    Tai, A. P. K.; Lombardozzi, D.; Val Martin, M.; Heald, C. L.

    2015-12-01

    Surface ozone is one of the most significant air pollutants due to its damaging effects not only on human health, but also on vegetation and crop productivity. Chronic ozone exposure has been shown to reduce photosynthesis and interfere with gas exchange in plants, which in turn affect the surface energy balance, carbon sink and other biogeochemical fluxes. Ozone damage on vegetation can thus have major ramifications on climate and atmospheric composition, including possible feedbacks onto ozone itself (see figure) that are not well understood. The damage of ozone on crops has been well documented, but a mechanistic understanding is not well established. Here we present several results pertaining to ozone-vegetation interaction. Using the Community Earth System Model, we find that inclusion of ozone damage on plants reduces the global land carbon sink by up to 5%, while simulated ozone is modified by -20 to +4 ppbv depending on the relative importance of competing mechanisms in different regions. We also perform a statistical analysis of multidecadal global datasets of crop yields, agroclimatic variables and ozone exposures to characterize the spatial variability of crop sensitivity to ozone and temperature extremes, specifically accounting for the confounding effect of ozone-temperature covariation. We find that several crops exhibit stronger sensitivity to ozone than found by previous field studies, with a strong anticorrelation between the sensitivity and average ozone levels that reflects biological adaptive ozone resistance. Our results show that a more complete understanding of ozone-vegetation interaction is necessary to derive more realistic future projections of climate, air quality and agricultural production, and thereby to formulate optimal strategies to safeguard public health and food security.

  1. [Correlation Analysis Between Characteristics of VOCs and Ozone Formation Potential in Summer in Nanjing Urban District].

    PubMed

    Yang, Xiao-xiao; Tang, Li-li; Zhang, Yun-jiang; Mu, Ying-feng; Wang, Ming; Chen, Wen-tai; Zhou, Hong-cang; Hua, Yan; Jiang, Rong-xin

    2016-02-15

    Volatile organic compounds (VOCs) is an important precursor of photochemical ozone pollution (O3) in the atmosphere. Their concentration variation directly affects the characteristics of the ozone pollution. The concentration, speciation of VOCs, ozone and its precursors in Nanjing were analyzed and measured using online gas detection systems in August 2013. VOCs/NOx discriminant method was used to get the sensitive control factors of ozone. The results showed that the averaged volume fraction of VOCs was 52. 05 x 10(-9), and the largest one reached 200 x 10(-9) in Nanjing urban district. The order of volume fraction of each species VOCs was alkane > oxygen-containing VOCs > alkene > aromatics. The averaged concentration of ozone was 76.5 microg x m(-1) and the exceeding concentration of hourly standard was 5.9%. The change trends of ozone precursors VOCs and NOx were basically identical and Ozone showed the obvious negative correlation during the period of high concentrations of ozone. There were some differences in the concentrations of the same VOCs in different ozone concentration periods. The ozone generation in Nanjing urban district was sensitive to VOCs, and Nanjing belonged to VOCs control area in summer. PMID:27363129

  2. Impact of cabin ozone concentrations on passenger reported symptoms in commercial aircraft.

    PubMed

    Bekö, Gabriel; Allen, Joseph G; Weschler, Charles J; Vallarino, Jose; Spengler, John D

    2015-01-01

    Due to elevated ozone concentrations at high altitudes, the adverse effect of ozone on air quality, human perception and health may be more pronounced in aircraft cabins. The association between ozone and passenger-reported symptoms has not been investigated under real conditions since smoking was banned on aircraft and ozone converters became more common. Indoor environmental parameters were measured at cruising altitude on 83 US domestic and international flights. Passengers completed a questionnaire about symptoms and satisfaction with the indoor air quality. Average ozone concentrations were relatively low (median: 9.5 ppb). On thirteen flights (16%) ozone levels exceeded 60 ppb, while the highest peak level reached 256 ppb for a single flight. The most commonly reported symptoms were dry mouth or lips (26%), dry eyes (22.1%) and nasal stuffiness (18.9%). 46% of passengers reported at least one symptom related to the eyes or mouth. A third of the passengers reported at least one upper respiratory symptom. Using multivariate logistic (individual symptoms) and linear (aggregated continuous symptom variables) regression, ozone was consistently associated with symptoms related to the eyes and certain upper respiratory endpoints. A concentration-response relationship was observed for nasal stuffiness and eye and upper respiratory symptom indicators. Average ozone levels, as opposed to peak concentrations, exhibited slightly weaker associations. Medium and long duration flights were significantly associated with more symptoms compared to short flights. The relationship between ultrafine particles and ozone on flights without meal service was indicative of ozone-initiated chemistry.

  3. [Correlation Analysis Between Characteristics of VOCs and Ozone Formation Potential in Summer in Nanjing Urban District].

    PubMed

    Yang, Xiao-xiao; Tang, Li-li; Zhang, Yun-jiang; Mu, Ying-feng; Wang, Ming; Chen, Wen-tai; Zhou, Hong-cang; Hua, Yan; Jiang, Rong-xin

    2016-02-15

    Volatile organic compounds (VOCs) is an important precursor of photochemical ozone pollution (O3) in the atmosphere. Their concentration variation directly affects the characteristics of the ozone pollution. The concentration, speciation of VOCs, ozone and its precursors in Nanjing were analyzed and measured using online gas detection systems in August 2013. VOCs/NOx discriminant method was used to get the sensitive control factors of ozone. The results showed that the averaged volume fraction of VOCs was 52. 05 x 10(-9), and the largest one reached 200 x 10(-9) in Nanjing urban district. The order of volume fraction of each species VOCs was alkane > oxygen-containing VOCs > alkene > aromatics. The averaged concentration of ozone was 76.5 microg x m(-1) and the exceeding concentration of hourly standard was 5.9%. The change trends of ozone precursors VOCs and NOx were basically identical and Ozone showed the obvious negative correlation during the period of high concentrations of ozone. There were some differences in the concentrations of the same VOCs in different ozone concentration periods. The ozone generation in Nanjing urban district was sensitive to VOCs, and Nanjing belonged to VOCs control area in summer.

  4. Impact of cabin ozone concentrations on passenger reported symptoms in commercial aircraft.

    PubMed

    Bekö, Gabriel; Allen, Joseph G; Weschler, Charles J; Vallarino, Jose; Spengler, John D

    2015-01-01

    Due to elevated ozone concentrations at high altitudes, the adverse effect of ozone on air quality, human perception and health may be more pronounced in aircraft cabins. The association between ozone and passenger-reported symptoms has not been investigated under real conditions since smoking was banned on aircraft and ozone converters became more common. Indoor environmental parameters were measured at cruising altitude on 83 US domestic and international flights. Passengers completed a questionnaire about symptoms and satisfaction with the indoor air quality. Average ozone concentrations were relatively low (median: 9.5 ppb). On thirteen flights (16%) ozone levels exceeded 60 ppb, while the highest peak level reached 256 ppb for a single flight. The most commonly reported symptoms were dry mouth or lips (26%), dry eyes (22.1%) and nasal stuffiness (18.9%). 46% of passengers reported at least one symptom related to the eyes or mouth. A third of the passengers reported at least one upper respiratory symptom. Using multivariate logistic (individual symptoms) and linear (aggregated continuous symptom variables) regression, ozone was consistently associated with symptoms related to the eyes and certain upper respiratory endpoints. A concentration-response relationship was observed for nasal stuffiness and eye and upper respiratory symptom indicators. Average ozone levels, as opposed to peak concentrations, exhibited slightly weaker associations. Medium and long duration flights were significantly associated with more symptoms compared to short flights. The relationship between ultrafine particles and ozone on flights without meal service was indicative of ozone-initiated chemistry. PMID:26011001

  5. Changes in the Vertical Distribution of Ozone Over Canada From Ozonesondes: 1980-2001

    NASA Astrophysics Data System (ADS)

    Wardle, D. I.; Tarasick, D. W.; Fioletov, V. E.; Kerr, J. B.; Davies, J.

    2005-12-01

    Measurements of the vertical profile of ozone concentration using balloon-borne ECC ozonesondes have been made weekly since 1980 at several sites in Canada (Edmonton, Goose Bay, Churchill and Resolute), since 1987 at Alert and since 1992 at Eureka. Previous analyses of ozone trends over Canada have shown strong negative trends in tropospheric ozone. Here, with data up to the end of 2001, we find that while for the 1980-2001 period the overall linear trends are primarily negative, both in tropospheric and stratospheric ozone, when the data for 1991-2001 only are considered, the trends are positive, even in the lower stratosphere. When the time series are compared with previously reported trends (to 1993), it is evident that ozone has rebounded at all levels below about 63 hPa. These differences do not appear to be related to changes in tropopause height, as the average height of the tropopause (as measured over the ozonesonde stations) has not changed over either the 22-year or the 11-year period. Nevertheless, comparison with another dynamical indicator, the wintertime frequency of occurrence of laminae in the ozone profile, suggests that this rebound may be partly a result of small changes in the atmospheric circulation, rather than a recovery of the ozone layer from halocarbon-induced depletion. The long-term trends in average tropospheric ozone concentrations over Canada are similar to corresponding lower stratospheric trends, and tropospheric ozone levels show significant correlation with lower stratospheric ozone amounts.

  6. Impact of Cabin Ozone Concentrations on Passenger Reported Symptoms in Commercial Aircraft

    PubMed Central

    Bekö, Gabriel; Allen, Joseph G.; Weschler, Charles J.; Vallarino, Jose; Spengler, John D.

    2015-01-01

    Due to elevated ozone concentrations at high altitudes, the adverse effect of ozone on air quality, human perception and health may be more pronounced in aircraft cabins. The association between ozone and passenger-reported symptoms has not been investigated under real conditions since smoking was banned on aircraft and ozone converters became more common. Indoor environmental parameters were measured at cruising altitude on 83 US domestic and international flights. Passengers completed a questionnaire about symptoms and satisfaction with the indoor air quality. Average ozone concentrations were relatively low (median: 9.5 ppb). On thirteen flights (16%) ozone levels exceeded 60 ppb, while the highest peak level reached 256 ppb for a single flight. The most commonly reported symptoms were dry mouth or lips (26%), dry eyes (22.1%) and nasal stuffiness (18.9%). 46% of passengers reported at least one symptom related to the eyes or mouth. A third of the passengers reported at least one upper respiratory symptom. Using multivariate logistic (individual symptoms) and linear (aggregated continuous symptom variables) regression, ozone was consistently associated with symptoms related to the eyes and certain upper respiratory endpoints. A concentration-response relationship was observed for nasal stuffiness and eye and upper respiratory symptom indicators. Average ozone levels, as opposed to peak concentrations, exhibited slightly weaker associations. Medium and long duration flights were significantly associated with more symptoms compared to short flights. The relationship between ultrafine particles and ozone on flights without meal service was indicative of ozone-initiated chemistry. PMID:26011001

  7. Tropospheric ozone and ozone profiles retrieved from GOME-2 and their validation

    NASA Astrophysics Data System (ADS)

    Miles, G. M.; Siddans, R.; Kerridge, B. J.; Latter, B. G.; Richards, N. A. D.

    2015-01-01

    This paper describes and assesses the performance of the RAL (Rutherford Appleton Laboratory) ozone profile retrieval scheme for the Global Ozone Monitoring Experiment 2 (GOME-2) with a focus on tropospheric ozone. Developments to the scheme since its application to GOME-1 measurements are outlined. These include the approaches developed to account sufficiently for UV radiometric degradation in the Hartley band and for inadequacies in knowledge of instrumental parameters in the Huggins bands to achieve the high-precision spectral fit required to extract information on tropospheric ozone. The assessment includes a validation against ozonesondes (sondes) sampled worldwide over 2 years (2007-2008). Standard deviations of the ensemble with respect to the sondes are considerably lower for the retrieved profiles than for the a priori, with the exception of the lowest subcolumn. Once retrieval vertical smoothing (averaging kernels) has been applied to the sonde profiles there is a retrieval bias of 6% (1.5 DU) in the lower troposphere, with smaller biases in the subcolumns above. The bias in the troposphere varies with latitude. The retrieval underestimates lower tropospheric ozone in the Southern Hemisphere (SH) (15-20% or ~ 1-3 DU) and overestimates it in the Northern Hemisphere (NH) (10% or 2 DU). The ability of the retrieval to reflect the geographical distribution of lower tropospheric ozone, globally (rather than just ozonesonde launch sites) is demonstrated by comparison with the chemistry transport model TOMCAT. For a monthly mean of cloud-cleared GOME-2 pixels, a correlation of 0.66 is found between the retrieval and TOMCAT sampled accordingly, with a bias of 0.7 Dobson Units. GOME-2 estimates higher concentrations in NH pollution centres but lower ozone in the Southern Ocean and South Pacific, which is consistent with the comparison to ozonesondes.

  8. What Would Have Happened to the Ozone Layer if Chlorofluorocarbons (CFCs) had not been Regulated?

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.; Oman, L. D.; Douglass, A. R.; Fleming, E. L.; Frith, S. M.; Hurwitz, M. M.; Kawa, S. R.; Jackman, C. H.; Krotkov, N. A.; Nash, E. R.; Nielsen, J. E.; Pawson, S.; Stolarski, R. S.; Velders, G. J. M.

    2008-01-01

    Ozone depletion by chlorofluorocarbons (CFCs) was first proposed by Molina and Rowland in their 1974 Nature paper. Since that time, the sci entific connection between ozone losses and CFCs and other ozone depl eting substances (ODSs) has been firmly established with laboratory m easurements, atmospheric observations, and modeling research. This science research led to the implementation of international agreements t hat largely stopped the production of ODSs. In this study we use a fu lly-coupled radiation-chemical-dynamical model to simulate a future world where ODSs were never regulated and ODS production grew at an ann ual rate of 3%. In this "world avoided" simulation 1.7 % of the globa lly-average column ozone is destroyed by 2020, and 67% is destroyed b y 2065 in comparison to 1980. Large ozone depletions in the polar region become year-round rather than just seasonal as is currently observ ed in the Antarctic ozone hole. Very large temperature decreases are observed in response to circulation changes and decreased shortwave radiation absorption by ozone. Ozone levels in the tropical lower strat osphere remain constant until about 2053 and then collapse to near ze ro by 2058 as a result of heterogeneous chemical processes (as curren tly observed in the Antarctic ozone hole). The tropical cooling that triggers the ozone collapse is caused by an increase of the tropical upwelling. In response to ozone changes, ultraviolet radiation increa ses, more than doubling the erythemal radiation in the northern summer midlatitudes by 2060.

  9. Ozone, Electrostatic Precipitators, and Particle Number Concentrations: Correlations Observed in a Real Office during Working Hours.

    PubMed

    Xiang, Jianbang; Weschler, Charles J; Mo, Jinhan; Day, Drew; Zhang, Junfeng; Zhang, Yinping

    2016-09-20

    This study investigates the impacts of outdoor and indoor ozone concentrations, ESP operation and occupancy on particle number concentrations within a modern office in Changsha, China. The office's one-pass air handling system contains a mini-bag filter (MERV 12) followed by an electrostatic precipitator (ESP) and high efficiency particulate air (HEPA) filter. Over a five-week period the system was operated either without the ESP (Stage 1, first-third week) or with the ESP (Stage 2, fourth and fifth week). Ozone and particle number concentrations were measured on working days. During both stages, indoor ozone and particle number concentrations tracked the outdoor ozone concentration. When operating, the ESP produced approximately 29 mg h(-1) of ozone, increasing supply air ozone by 15 ppb and steady-state indoor ozone by about 3 ppb. Occupancy tended to decrease indoor ozone and increase particle levels. During occupancy, indoor particle levels were low (∼2600 particle/cm(3)) when the supply air ozone level was less than 18 ppb. Above this threshold, the supply air ozone concentration and indoor particle number concentration were linearly related, and ESP operation increased the average indoor particle level by about 22 000 particles/cm(3). The implications for worker exposure to both ozone and particles are discussed. PMID:27571436

  10. Ozone, Electrostatic Precipitators, and Particle Number Concentrations: Correlations Observed in a Real Office during Working Hours.

    PubMed

    Xiang, Jianbang; Weschler, Charles J; Mo, Jinhan; Day, Drew; Zhang, Junfeng; Zhang, Yinping

    2016-09-20

    This study investigates the impacts of outdoor and indoor ozone concentrations, ESP operation and occupancy on particle number concentrations within a modern office in Changsha, China. The office's one-pass air handling system contains a mini-bag filter (MERV 12) followed by an electrostatic precipitator (ESP) and high efficiency particulate air (HEPA) filter. Over a five-week period the system was operated either without the ESP (Stage 1, first-third week) or with the ESP (Stage 2, fourth and fifth week). Ozone and particle number concentrations were measured on working days. During both stages, indoor ozone and particle number concentrations tracked the outdoor ozone concentration. When operating, the ESP produced approximately 29 mg h(-1) of ozone, increasing supply air ozone by 15 ppb and steady-state indoor ozone by about 3 ppb. Occupancy tended to decrease indoor ozone and increase particle levels. During occupancy, indoor particle levels were low (∼2600 particle/cm(3)) when the supply air ozone level was less than 18 ppb. Above this threshold, the supply air ozone concentration and indoor particle number concentration were linearly related, and ESP operation increased the average indoor particle level by about 22 000 particles/cm(3). The implications for worker exposure to both ozone and particles are discussed.

  11. An evaluation of ozone exposure metrics for a seasonally drought-stressed ponderosa pine ecosystem.

    PubMed

    Panek, Jeanne A; Kurpius, Meredith R; Goldstein, Allen H

    2002-01-01

    Ozone stress has become an increasingly significant factor in cases of forest decline reported throughout the world. Current metrics to estimate ozone exposure for forest trees are derived from atmospheric concentrations and assume that the forest is physiologically active at all times of the growing season. This may be inaccurate in regions with a Mediterranean climate, such as California and the Pacific Northwest, where peak physiological activity occurs early in the season to take advantage of high soil moisture and does not correspond to peak ozone concentrations. It may also misrepresent ecosystems experiencing non-average climate conditions such as drought years. We compared direct measurements of ozone flux into a ponderosa pine canopy with a suite of the most common ozone exposure metrics to determine which best correlated with actual ozone uptake by the forest. Of the metrics we assessed, SUM0 (the sum of all daytime ozone concentrations > 0) best corresponded to ozone uptake by ponderosa pine, however the correlation was only strong at times when the stomata were unconstrained by site moisture conditions. In the early growing season (May and June). SUM0 was an adequate metric for forest ozone exposure. Later in the season, when stomatal conductance was limited by drought. SUM0 overestimated ozone uptake. A better metric for seasonally drought-stressed forests would be one that incorporates forest physiological activity, either through mechanistic modeling, by weighting ozone concentrations by stomatal conductance, or by weighting concentrations by site moisture conditions. PMID:11843543

  12. What would have happened to the ozone layer if chlorofluorocarbons (CFCs) had not been regulated?

    NASA Astrophysics Data System (ADS)

    Newman, P. A.; Oman, L. D.; Douglass, A. R.; Fleming, E. L.; Frith, S. M.; Hurwitz, M. M.; Kawa, S. R.; Jackman, C. H.; Krotkov, N. A.; Nash, E. R.; Nielsen, J. E.; Pawson, S.; Stolarski, R. S.; Velders, G. J.

    2008-12-01

    Ozone depletion by chlorofluorocarbons (CFCs) was first proposed by Molina and Rowland in their 1974 Nature paper. Since that time, the scientific connection between ozone losses and CFCs and other ozone depleting substances (ODSs) has been firmly established with laboratory measurements, atmospheric observations, and modeling research. The nations of the world implemented the Montreal Protocol (and amendments) which stopped ODS production in 1992. In this presentation we use a fully coupled radiation- chemical-dynamical model to simulate a future world where ODSs were never regulated and ODS production grew at an annual rate of 3%. In this "world avoided" simulation, 17% of the globally average column ozone is destroyed by 2020, and 67% is destroyed by 2065 in comparison to 1980. Large ozone depletions in the polar region become year-round rather than just seasonal as is currently observed in the Antarctic ozone hole. Very large temperature decreases are observed in response to circulation changes and decreased shortwave radiation absorption by ozone. Ozone levels in the tropical lower stratosphere remain constant until about 2053 and then collapse to near zero by 2058 as a result of heterogeneous chemical processes (as currently observed in the Antarctic ozone hole). The tropical cooling that triggers the ozone collapse is caused by an increase of the tropical upwelling. In response to ozone changes, ultraviolet (UV) radiation increases, tripling the erythemal (sunburn) radiation in the northern summer mid-latitudes by 2065.

  13. Long-term total ozone response caused by extra-terrestrial factors

    NASA Astrophysics Data System (ADS)

    Krivolutsky, A.; Knyazeva, N.; Perejaslova, G.; Bazilevskaya, G.; Nazarova, M.

    The observations of solar proton fluxes from boards of "Meteor", GOES satellites, galactic cosmic ray fluxes measured in the stratosphere by balloons, solar radio irradiance and total ozone records (ground based and TOMS data) for 1960-2000 period, has been used to investigate spatial and temporal structure of total ozone response to cosmic influence. Linear simple and multiply regression analysis has been used in our study. Yearly averaged data were used for analysis to e timates long-t erm effects in ozone response. Ozone data were grouped in different latitudinal belts of 100 width for Northern Hemisphere from equator to 800 N. Simple linear regression analysis for individual cosmic factors revealed negative total ozone response (in accordance to the conception of ozone destruction by additional amount of NOx produced by solar protons in the atmosphere of the Earth)0 for the years of strong solar proton events for latitudes which were higher than 45 N However, positive response for lower latitudes was found, when the same regression method was used. In the case of GCR influence on ozone the decadal response of ozone was revealed at high latitudes, which was in phase with galactic cosmic ray flux and in contract to the mentioned conception of ozone destruction by the NOx . Multiply regression analysis gave the long-term ozone variation of cosmic nature similar to real variations of total ozone.

  14. Ozone Depletion by Hydrofluorocarbons

    NASA Astrophysics Data System (ADS)

    Hurwitz, M.; Fleming, E. L.; Newman, P. A.; Li, F.; Mlawer, E. J.; Cady-Pereira, K. E.; Bailey, R.

    2015-12-01

    Hydrofluorocarbons (HFCs) are second-generation replacements for the chlorofluorocarbons (CFCs), halons and other substances that caused the 'ozone hole'. Atmospheric concentrations of HFCs are projected to increase dramatically in the coming decades. Coupled chemistry-climate simulations forced by these projections show that HFCs will impact the global atmosphere in 2050. As strong radiative forcers, HFCs modulate atmospheric temperature, thereby changing ozone-destroying catalytic cycles and enhancing the stratospheric circulation. These changes lead to a weak depletion of stratospheric ozone. Sensitivity simulations with the NASA Goddard Space Flight Center (GSFC) 2D model show that HFC-125 is the most important contributor to atmospheric change in 2050, as compared with HFC-23, HFC-32, HFC-134a and HFC-143a. Incorporating the interactions between chemistry, radiation and dynamics, for a likely 2050 climate, ozone depletion potentials (ODPs) for HFCs range from 4.3x10-4 to 3.5x10-2; previously HFCs were assumed to have negligible ODPs since these species lack chlorine or bromine atoms. The ozone impacts of HFCs are further investigated with the Goddard Earth Observing System Chemistry-Climate Model (GEOSCCM). The GEOSCCM is a three-dimensional, fully coupled ocean-atmosphere model with interactive stratospheric chemistry. Sensitivity simulations in which CO2, CFC-11 and HCFC-22 are enhanced individually are used as proxies for the atmospheric response to the HFC concentrations expected by the mid-21st century. Sensitivity simulations provide quantitative estimates of the impacts of these greenhouse gases on global total ozone, and can be used to assess their effects on the recovery of Antarctic ozone.

  15. The influence of meteorological factors and biomass burning on surface ozone concentrations at Tanah Rata, Malaysia

    NASA Astrophysics Data System (ADS)

    Toh, Ying Ying; Lim, Sze Fook; von Glasow, Roland

    2013-05-01

    The surface ozone concentrations at the Tanah Rata regional Global Atmosphere Watch (GAW) station, Malaysia (4°28‧N, 101°23‧E, 1545 m above Mean Sea Level (MSL)) from June 2006 to August 2008 were analyzed in this study. Overall the ozone mixing ratios are very low; the seasonal variations show the highest mixing ratios during the Southwest monsoon (average 19.1 ppb) and lowest mixing ratios during the spring intermonsoon (average 14.2 ppb). The diurnal variation of ozone is characterised by an afternoon maximum and night time minimum. The meteorological conditions that favour the formation of high ozone levels at this site are low relative humidity, high temperature and minimum rainfall. The average ozone concentration is lower during precipitation days compared to non-precipitation days. The hourly averaged ozone concentrations show significant correlations with temperature and relative humidity during the Northeast monsoon and spring intermonsoon. The highest concentrations are observed when the wind is blowing from the west. We found an anticorrelation between the atmospheric pressure tide and ozone concentrations. The ozone mixing ratios do not exceed the recommended Malaysia Air Quality Guidelines for 1-h and 8-h averages. Five day backward trajectories on two high ozone episodes in 07 August 2006 (40.0 ppb) and 24 February 2008 (45.7 ppb) are computed using the HYbrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) model to investigate the origin of the pollutants and influence of regional transport. The high ozone episode during 07 August 2006 (burning season during southwest monsoon) is mainly attributed to regional transport from biomass burning in Sumatra, whereas favourable meteorological conditions (i.e. low relative humidity, high temperature and solar radiation, zero rainfall) and long range transport from Indo-China have elevated the ozone concentrations during 24 February 2008.

  16. Have primary emission reduction measures reduced ozone across Europe? An analysis of European rural background ozone trends 1996-2005

    NASA Astrophysics Data System (ADS)

    Wilson, R. C.; Fleming, Z. L.; Monks, P. S.; Clain, G.; Henne, S.; Konovalov, I. B.; Szopa, S.; Menut, L.

    2012-01-01

    National and European legislation over the past 20 yr, and the modernisation or removal of industrial sources, have significantly reduced European ozone precursor emissions. This study quantifies observed and modelled European ozone annual and seasonal linear trends from 158 harmonised rural background monitoring stations over a constant time period of a decade (1996-2005). Mean ozone concentrations are investigated, in addition to the ozone 5th percentiles as a measure of the baseline or background conditions, and the 95th percentiles that are representative of the peak concentration levels. This study aims to characterise and quantify surface European ozone concentrations and trends and assess the impact of the changing anthropogenic emission tracers on the observed and modelled trends. Significant (p<0.1) positive annual trends in ozone mean, 5th and 95th percentiles are observed at 54 %, 52 % and 45 % of sites respectively (85 sites, 82 sites and 71 sites). Spatially, sites in central and north-western Europe tend to display positive annual ozone trends in mean, 5th and 95th percentiles. Significant negative annual trends in ozone mean 5th and 95th percentiles are observed at 11 %, 12 % and 12 % of sites respectively (18 sites, 19 sites and 19 sites) which tend to be located in the eastern and south-western extremities of Europe. European-averaged annual trends have been calculated from the 158 sites in this study. Overall there is a net positive annual trend in observed ozone mean (0.16±0.02 ppbv yr-1 (2σ error)), 5th (0.13±0.02 ppbv yr-1) and 95th (0.16±0.03 ppbv yr-1) percentiles, representative of positive trends in mean, baseline and peak ozone. Assessing the sensitivity of the derived overall trends to the constituent years shows that the European heatwave year of 2003 has significant positive influence and 1998 the converse effect; demonstrating the masking effect of inter-annual variability on decadal based ozone trends. The European scale 3-D CTM

  17. Projected changes in high ozone pollution events over the Eastern United States over the 21st century

    NASA Astrophysics Data System (ADS)

    Fiore, A. M.; Rieder, H.; Horowitz, L. W.; Naik, V.

    2013-12-01

    Over the past few decades, thresholds for the United States (US) National Ambient Air Quality Standard (NAAQS) for ozone (O3), established to protect public health and welfare, have been lowered repeatedly. We recently applied methods from extreme value theory (EVT) to maximum daily 8-hour average ozone (MDA8 O3) observed by the Clean Air Status and Trends Network (CASTNet) to quantify the significant decline in both frequency and magnitude of high O3 pollution events over the Eastern US from 1988 to 2009. These improvements to Eastern US air quality have been reported in prior studies and result from changes in air quality regulations and subsequent control measures (e.g., the 'NOx SIP Call') as demonstrated by our analysis of 1-year and 5-year return levels. Here we extend this analysis to future projections of high O3 pollution events spanning the course of the 21st century. To this aim, we analyze simulations from the GFDL CM3 chemistry-climate model under selected Representative Concentration Pathway (RCP) scenarios: RCP4.5 and RCP8.5 (representing a moderate and strong climate warming with a global mean temperature change by 2100 compared to present day of +2.3K and +4.5K, respectively). Under both scenarios, NOx emissions decrease by ~80% over North America by 2100 under the assumption of aggressive ozone pollution controls. A third scenario, termed RCP4.5_WMGG, in which well-mixed greenhouse gases follow the RCP4.5 scenario but O3 and aerosol precursor emissions are held at 2005 levels, enables us to isolate the role of climate change from that of emission reductions. As we find a positive bias in GFDL CM3 MDA8 O3 compared to the Eastern US CASTNet O3 measurements during summer (a common feature in the current generation of models), we develop a correction method based on quantile-mapping. This bias correction effectively removes the model bias while preserving the temporal changes in MDA8 O3 as simulated under different RCPs over the course of the 21st

  18. Projected changes in high ozone pollution events over the Eastern United States over the 21st century

    NASA Astrophysics Data System (ADS)

    Rieder, Harald E.; Fiore, Arlene M.; Horrowitz, Larry W.; Naik, Vaishali

    2014-05-01

    Over the past few decades, thresholds for the United States (US) National Ambient Air Quality Standard (NAAQS) for ozone (O3), established to protect public health and welfare, have been lowered repeatedly. We recently applied methods from extreme value theory (EVT) to maximum daily 8-hour average ozone (MDA8 O3) observed by the Clean Air Status and Trends Network (CASTNet) to quantify the significant decline in both frequency and magnitude of high O3 pollution events over the Eastern US from 1988 to 2009. These improvements to Eastern US air quality have been reported in prior studies and result from changes in air quality regulations and subsequent control measures (e.g., the "NOx SIP Call") as demonstrated by our analysis of 1-year and 5-year return levels. Here we extend this analysis to future projections of high O3 pollution events spanning the course of the 21st century. To this aim, we analyze simulations from the GFDL CM3 chemistry-climate model under selected Representative Concentration Pathway (RCP) scenarios: RCP4.5 and RCP8.5 (representing a moderate and strong climate warming with a global mean temperature change by 2100 compared to present day of +2.3K and +4.5K, respectively). Under both scenarios, NOx emissions decrease by ~80% over North America by 2100 under the assumption of aggressive ozone pollution controls. A third scenario, termed RCP4.5_WMGG, in which well-mixed greenhouse gases follow the RCP4.5 scenario but O3 and aerosol precursor emissions are held at 2005 levels, enables us to isolate the role of climate change from that of emission reductions. As we find a positive bias in GFDL CM3 MDA8 O3 compared to the Eastern US CASTNet O3 measurements during summer (a common feature in the current generation of models), we develop a correction method based on quantile-mapping. This bias correction effectively removes the model bias while preserving the temporal changes in MDA8 O3 as simulated under different RCPs over the course of the 21st

  19. Children's Models of the Ozone Layer and Ozone Depletion.

    ERIC Educational Resources Information Center

    Christidou, Vasilia; Koulaidis, Vasilis

    1996-01-01

    The views of 40 primary students on ozone and its depletion were recorded through individual, semi-structured interviews. The data analysis resulted in the formation of a limited number of models concerning the distribution and role of ozone in the atmosphere, the depletion process, and the consequences of ozone depletion. Identifies five target…

  20. Ozone Contamination in Aircraft Cabins. Appendix A: Ozone toxicity

    NASA Technical Reports Server (NTRS)

    Melton, C. E.

    1979-01-01

    The recommendation that at various altitudes the amount of air with which ozone has mixed changes, thus changing the volume per volume relationship is discussed. The biological effects of ozone on human health and the amount of ozone necessary to produce symptoms were investigated.

  1. CONTRIBUTION TO INDOOR OZONE LEVELS OF AN OZONE GENERATOR

    EPA Science Inventory

    This report gives results of a study of a commonly used commercially available ozone generator, undertaken to determine its impact on indoor ozone levels. xperiment were conducted in a typical mechanically ventilated office and in a test house. he generated ozone and the in-room ...

  2. Detecting the Recovery of the Antarctic Ozone Hole

    NASA Technical Reports Server (NTRS)

    Newman, Paul A.; Nash, Eric R.; Kawa, S. Randolph; Montzka, Steve

    2004-01-01

    The Antarctic ozone hole develops each year and culminates by early Spring. Antarctic ozone values have been monitored since 1979 using satellite observations from the TOMS instrument. The severity of the hole has been assessed from TOMS using the minimum total ozone value from the October monthly mean (depth of the hole) and by calculating the average size during the September-October period. Ozone is mainly destroyed by halogen catalytic cycles, and these losses are modulated by temperature variations in the collar of the polar lower stratospheric vortex. In this presentation, we show the relationships of halogens and temperature to both the size and depth of the hole. Because atmospheric halogen levels are responding to international agreements that limit or phase out production, the amount of halogens in the stratosphere should decrease over the next few decades. Using projections of halogen levels combined with age-of-air estimates, we find that the ozone hole is recovering at an extremely slow rate and that large ozone holes will regularly recur over the next 2 decades. We will show estimates of both when the ozone hole will begin to show first signs of recovery, and when the hole will fully recover to pre-1980 levels.

  3. Synoptic and meteorological drivers of extreme ozone concentrations over Europe

    NASA Astrophysics Data System (ADS)

    Otero, N.; Sillmann, J.; Schnell, J. L.; Rust, H. W.; Butler, T.

    2016-02-01

    The present work assesses the relationship between local and synoptic meteorological conditions and surface ozone concentration over Europe in spring and summer months, during the period 1998-2012 using a new interpolated data set of observed surface ozone concentrations over the European domain. Along with local meteorological conditions, the influence of large-scale atmospheric circulation on surface ozone is addressed through a set of airflow indices computed with a novel implementation of a grid-by-grid weather type classification across Europe. Drivers of surface ozone over the full distribution of maximum daily 8 h average values are investigated, along with drivers of the extreme high percentiles and exceedances or air quality guideline thresholds. Three different regression techniques are applied: multiple linear regression to assess the drivers of maximum daily ozone, logistic regression to assess the probability of threshold exceedances and quantile regression to estimate the meteorological influence on extreme values, as represented by the 95th percentile. The relative importance of the input parameters (predictors) is assessed by a backward stepwise regression procedure that allows the identification of the most important predictors in each model. Spatial patterns of model performance exhibit distinct variations between regions. The inclusion of the ozone persistence is particularly relevant over southern Europe. In general, the best model performance is found over central Europe, where the maximum temperature plays an important role as a driver of maximum daily ozone as well as its extreme values, especially during warmer months.

  4. Perspectives on African Ozone from Sondes, Dobson and Aircraft Measurements

    NASA Technical Reports Server (NTRS)

    Thompson, A. M.; Witte, J. C.; Chatfield, R. B.; Diab, R. D.; Thouret, V.; Sauvage, B.

    2004-01-01

    We have been studying variability in ozone over Africa using data from ozonesondes (vertical profiles from surface to stratosphere), aircraft (the MOZAIC dataset with cruise altitude and landing/takeoff profiles) and the ground (Dobson spectrophotometer total ozone column measurement). The following may give context for ozone investigations during AMMA: 1. Total ozone measurements since 1989 show considerable variability in mean value among the African stations in Algeria, Kenya, Egypt, South Africa, as well as in seasonal cycles and year-to-year. Trends are not evident. 2. The impacts of convection, stratospheric injection, biomass burning and lightning appear in ozone sounding profile data. Time-series analysis and case studies point to periodic influences of long-range interactions with the Atlantic ("ozone paradox," wave-one") and Indian Oceans. 3. Tropospheric ozone variations, observed in tropospheric profiles and integrated column amount, follow general seasonal patterns but short- term variability is so strong that simple averages are inadequate for describing "climatology" and statistical classification approaches may be required.

  5. "OZONE SOURCE APPORTIONMENT IN CMAQ'

    EPA Science Inventory

    Ozone source attribution has been used to support various policy purposes including interstate transport (Cross State Air Pollution Rule) by U.S. EPA and ozone nonattainment area designations by State agencies. Common scientific applications include tracking intercontinental tran...

  6. Ozone Minimums, 1979 to 2013

    NASA Video Gallery

    Minimum concentration of ozone in the southern hemisphere for each year from 1979-2013 (there is no data from 1995). Each image is the day of the year with the lowest concentration of ozone. A grap...

  7. Stratospheric Ozone Predictions For The Late 21st Century

    NASA Astrophysics Data System (ADS)

    Douglass, A. R.; Olsen, M. A.; Stolarski, R. S.; Strahan, S. E.; Oman, L.

    2013-12-01

    Simulations of ozone evolution from 1960 until ~2100 from chemistry climate models (CCMs) that participated in CCMVal-2 are broadly consistent in that stratospheric ozone increases as chlorofluorcarbons decrease and the stratosphere cools (which affects the rate of temperature dependent loss processes), however, details of the projections vary significantly. Differences in the ozone response to specified changes in chlorine containing source gases dominate during the first half of the integrations. For example, from 1980 to 2000, chlorine change is by far the most important cause of ozone change, and the CCMs produce changes in the 60S-60N average column ozone that range between -3 DU and -17 DU. In the second half of the 21st century climate change is primarily responsible for ozone change. By 2080 the CCMs produce changes in the 60S-60N average upper stratospheric ozone column that range from 4 DU to 10 DU. The CCM range of differences is due to differences in both composition and upper stratospheric temperature. Ozone loss processes each have their own temperature sensitivity, and the net sensitivity of ozone to temperature change in each CCM depends on the relative importance of each loss process; this depends on the composition and temperature for the baseline atmosphere. In the lower stratosphere, climate change affects ozone evolution through changes in photochemical reaction rates due to stratospheric cooling and through circulation differences affecting transport of ozone and other trace gases. These are not separable using an approach such as multiple linear regression because changes in circulation and temperature have the same time dependence after accounting for contributions due to chlorine change. Recent attention has focused on similarity of the CCMs in that all predict a speed-up of the Brewer Dobson circulation. However, differences in the magnitude of the speed-up, differences in horizontal mixing and differences in the photochemical response to

  8. 77 FR 73387 - Approval and Promulgation of Air Quality Implementation Plans; Pennsylvania; Determinations of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-10

    ... 2007-2009, 2008-2010, and 2009-2011 data. Table 1--2007-2009 Pittsburgh Area 8-Hour Ozone Design Values... Table 3--2009-2011 Pittsburgh Area 8-Hour Ozone Design Values 2009-2011 Average County Monitor ID % data... certified ambient air monitoring data for the 2007-2009 monitoring period showing monitored attainment...

  9. 76 FR 41444 - Approval and Promulgation of Air Quality Implementation Plans; Commonwealth of Virginia; Section...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-14

    ... INFORMATION: ] I. Background On July 18, 1997, EPA promulgated a revised 8-hour ozone NAAQS (62 FR 38856) and a new PM 2.5 NAAQS (62 FR 38652). The revised ozone NAAQS is based on 8-hour average concentrations...\\ to 35 g/m\\3\\ on October 17, 2006 (71 FR 61144). Section 110(a) of the CAA requires States to...

  10. Winter rain and summer ozone: a predictive relationship.

    PubMed

    Sandberg, J S; Basso, M J; Okin, B A

    1978-06-01

    Insights from dendrochronology have provided a new seasonal predictor for air pollution meteorology. In the San Francisco Bay Area summer ozone excesses over the federal ozone standard are correlated (correlation coefficient r = .87) with precipitation for the two preceding winters, a factor related to tree-ring width in a precipitation-stressed climate. The hypothesis that reactive hydrocarbon emissions from vegetative biomass affects these ozone excesses was supported by a similar correlation between summer hydrocarbon average maximums and the two-winter precipitation factor, reaching r = .88 at suburban stations. A weak tendency for hot summers to follow wet winters (in 16 years of California data) explains only a minor part of the ozone-rain relationship in multiple correlations.

  11. Developing a predictive tropospheric ozone model for Tabriz

    NASA Astrophysics Data System (ADS)

    Khatibi, Rahman; Naghipour, Leila; Ghorbani, Mohammad A.; Smith, Michael S.; Karimi, Vahid; Farhoudi, Reza; Delafrouz, Hadi; Arvanaghi, Hadi

    2013-04-01

    Predictive ozone models are becoming indispensable tools by providing a capability for pollution alerts to serve people who are vulnerable to the risks. We have developed a tropospheric ozone prediction capability for Tabriz, Iran, by using the following five modeling strategies: three regression-type methods: Multiple Linear Regression (MLR), Artificial Neural Networks (ANNs), and Gene Expression Programming (GEP); and two auto-regression-type models: Nonlinear Local Prediction (NLP) to implement chaos theory and Auto-Regressive Integrated Moving Average (ARIMA) models. The regression-type modeling strategies explain the data in terms of: temperature, solar radiation, dew point temperature, and wind speed, by regressing present ozone values to their past values. The ozone time series are available at various time intervals, including hourly intervals, from August 2010 to March 2011. The results for MLR, ANN and GEP models are not overly good but those produced by NLP and ARIMA are promising for the establishing a forecasting capability.

  12. Winter rain and summer ozone: a predictive relationship.

    PubMed

    Sandberg, J S; Basso, M J; Okin, B A

    1978-06-01

    Insights from dendrochronology have provided a new seasonal predictor for air pollution meteorology. In the San Francisco Bay Area summer ozone excesses over the federal ozone standard are correlated (correlation coefficient r = .87) with precipitation for the two preceding winters, a factor related to tree-ring width in a precipitation-stressed climate. The hypothesis that reactive hydrocarbon emissions from vegetative biomass affects these ozone excesses was supported by a similar correlation between summer hydrocarbon average maximums and the two-winter precipitation factor, reaching r = .88 at suburban stations. A weak tendency for hot summers to follow wet winters (in 16 years of California data) explains only a minor part of the ozone-rain relationship in multiple correlations. PMID:17740697

  13. Tropospheric ozone distributions measured with an airborne laser absorption spectrometer

    NASA Technical Reports Server (NTRS)

    Menzies, R. T.; Shumate, M. S.

    1978-01-01

    Measurements of tropospheric ozone have been made in the southern and middle California regions and over the Pacific Ocean during two series of flights in February and May 1977. The data were obtained by using a laser absorption spectrometer, a nadir-viewing instrument which remotely measures the ozone column abundance between ground level and aircraft altitude by interacting with ozone at specific wavelengths near 9.5 microns. The measurements indicate significantly lower ozone abundances above the Mojave Desert region as compared with farm, forest, and urban areas. The average tropospheric column density was found to be 0.0027 atm cm/km over the California region and 0.0035 atm cm/km over the Pacific Ocean region 1000-2000 km west of the coast of Mexico.

  14. Approach to forecasting daily maximum ozone levels in St. Louis

    NASA Technical Reports Server (NTRS)

    Prior, E. J.; Schiess, J. R.; Mcdougal, D. S.

    1981-01-01

    Measurements taken in 1976 from the St. Louis Regional Air Pollution Study (RAPS) data base, conducted by EPA, were analyzed to determine an optimum set of air-quality and meteorological variables for predicting maximum ozone levels for each day in 1976. A 'leaps and bounds' regression analysis was used to identify the best subset of variables. Three particular variables, the 9 a.m. ozone level, the forecasted maximum temperature, and the 6-9 a.m. averaged wind speed, have useful forecasting utility. The trajectory history of air masses entering St. Louis was studied, and it was concluded that transport-related variables contribute to the appearance of very high ozone levels. The final empirical forecast model predicts the daily maximum ozone over 341 days with a standard deviation of 11 ppb, which approaches the estimated error.

  15. Dissociating Averageness and Attractiveness: Attractive Faces Are Not Always Average

    ERIC Educational Resources Information Center

    DeBruine, Lisa M.; Jones, Benedict C.; Unger, Layla; Little, Anthony C.; Feinberg, David R.

    2007-01-01

    Although the averageness hypothesis of facial attractiveness proposes that the attractiveness of faces is mostly a consequence of their averageness, 1 study has shown that caricaturing highly attractive faces makes them mathematically less average but more attractive. Here the authors systematically test the averageness hypothesis in 5 experiments…

  16. Ozone depletion by hydrofluorocarbons

    NASA Astrophysics Data System (ADS)

    Hurwitz, Margaret M.; Fleming, Eric L.; Newman, Paul A.; Li, Feng; Mlawer, Eli; Cady-Pereira, Karen; Bailey, Roshelle

    2015-10-01

    Atmospheric concentrations of hydrofluorocarbons (HFCs) are projected to increase considerably in the coming decades. Chemistry climate model simulations forced by current projections show that HFCs will impact the global atmosphere increasingly through 2050. As strong radiative forcers, HFCs increase tropospheric and stratospheric temperatures, thereby enhancing ozone-destroying catalytic cycles and modifying the atmospheric circulation. These changes lead to a weak depletion of stratospheric ozone. Simulations with the NASA Goddard Space Flight Center 2-D model show that HFC-125 is the most important contributor to HFC-related atmospheric change in 2050; its effects are comparable to the combined impacts of HFC-23, HFC-32, HFC-134a, and HFC-143a. Incorporating the interactions between chemistry, radiation, and dynamics, ozone depletion potentials (ODPs) for HFCs range from 0.39 × 10-3 to 30.0 × 10-3, approximately 100 times larger than previous ODP estimates which were based solely on chemical effects.

  17. Impacts of Ozone-vegetation Interactions and Biogeochemical Feedbacks on Atmospheric Composition and Air Quality Under Climate Change

    NASA Astrophysics Data System (ADS)

    Sadeke, M.; Tai, A. P. K.; Lombardozzi, D.; Val Martin, M.

    2015-12-01

    Surface ozone pollution is one of the major environmental concerns due to its damaging effects on human and vegetation. One of the largest uncertainties of future surface ozone prediction comes from its interaction with vegetation under a changing climate. Ozone can be modulated by vegetation through, e.g., biogenic emissions, dry deposition and transpiration. These processes are in turn affected by chronic exposure to ozone via lowered photosynthesis rate and stomatal conductance. Both ozone and vegetation growth are expected to be altered by climate change. To better understand these climate-ozone-vegetation interactions and possible feedbacks on ozone itself via vegetation, we implement an online ozone-vegetation scheme [Lombardozzi et al., 2015] into the Community Earth System Model (CESM) with active atmospheric chemistry, climate and land surface components. Previous overestimation of surface ozone in eastern US, Canada and Europe is shown to be reduced by >8 ppb, reflecting improved model-observation comparison. Simulated surface ozone is lower by 3.7 ppb on average globally. Such reductions (and improvements) in simulated ozone are caused mainly by lower isoprene emission arising from reduced leaf area index in response to chronic ozone exposure. Effects via transpiration are also potentially significant but require better characterization. Such findings suggest that ozone-vegetation interaction may substantially alter future ozone simulations, especially under changing climate and ambient CO2 levels, which would further modulate ozone-vegetation interactions. Inclusion of such interactions in Earth system models is thus necessary to give more realistic estimation and prediction of surface ozone. This is crucial for better policy formulation regarding air quality, land use and climate change mitigation. Reference list: Lombardozzi, D., et al. "The Influence of Chronic Ozone Exposure on Global Carbon and Water Cycles." Journal of Climate 28.1 (2015): 292-305.

  18. Application of ozone for reduction of mycological infection in wheat grain.

    PubMed

    Raila, Algirdas; Lugauskas, Albinas; Steponavicius, Dainius; Railiene, Marija; Steponaviciene, Ausra; Zvicevicius, Egidijus

    2006-01-01

    In 2004-2005 means were sought to clean grain from microbiological contamination during transportation and storage. For this purpose, grains with a moisture content of 23.2 % of the "Tauras" variety were selected and ventilated daily for 8 hours until grain wetness was reduced to 14.0 %. The effect of ventilation duration and ozone impact was evaluated according to the changes in grain contamination with micromycetes propagules (cfu x g (-1)), and alternation of micromycetes species on the grain surface. At drying grains by active ventilation with an ozone--air mixture, at O (3) concentration of 700 ppb, the drying period was reduced by about 20 %, and mycological contamination depends on initial grain moisture content (w): when w=15.2 %, contamination was reduced by up to 2.2 times, and when w=22.0 %--up to 3 times. At the same time, the composition of micromycetes species on the grain surface changed significantly: in non-ventilated grain there were detected micromycetes of 26 species, and in ventilated grain--of 11 species. Efficient ozone impact was established only when the mound of wet (w>18.0 %) grains was exposed to ozone.

  19. Tropospheric ozone measurements at the equatorial region (1980-1988)

    NASA Technical Reports Server (NTRS)

    Ilyas, Mohammad

    1994-01-01

    Results from surface ozone measurements at Penang (5.5 deg N, 100 deg E) over 1980-88 period are presented. The study indicates the ozone concentrations undergoing significant diurnal and seasonal variations. The peak concentration are observed at around mid-day (up to 35 nb) but the O3 concentration generally drops to zero level in the early evening and remains unchanged until mid-morning. Monthly-averaged daily 1-h average concentrations are generally small (4-13 nb) and decrease continually from the early part of the year to the end. Frequently, varying local weather conditions seem to influence the O3 concentrations.

  20. Have primary emission reduction measures reduced ozone across Europe? An analysis of European rural background ozone trends 1996-2005

    NASA Astrophysics Data System (ADS)

    Wilson, R. C.; Fleming, Z. L.; Monks, P. S.; Clain, G.; Henne, S.; Konovalov, I. B.; Szopa, S.; Menut, L.

    2011-06-01

    National and European legislation over the past 20 years, and the modernisation or removal of industrial sources, have significantly reduced European ozone precursor emissions. This study quantifies observed and modelled European ozone annual and seasonal linear trends from 158 harmonised rural background monitoring stations over a constant time period of a decade (1996-2005). Mean ozone concentrations are investigated, in addition to the ozone 5th percentiles as a measure of the baseline or background conditions, and the 95th percentiles that are representative of the peak concentration levels. This study aims to characterise and quantify surface European ozone concentrations and trends and assess the impact of the changing anthropogenic emission tracers on the observed and modelled trends. Significant (p < 0.1) positive annual trends in ozone mean, 5th and 95th percentiles are observed at 54 %, 52 % and 45 % of sites respectively (85 sites, 82 sites and 71 sites). Spatially, sites in Central and Northwestern Europe tend to display positive annual ozone trends in mean, 5th and 95th percentiles. Significant negative annual trends in ozone mean 5th and 95th percentiles are observed at 11 %, 12 % and 12 % of sites respectively (18 sites, 19 sites and 19 sites) which tend to be located in the eastern and south-western extremities of Europe. European-averaged annual trends have been calculated from the 158 sites in this study. Overall there is a net positive annual trend in observed ozone mean (0.16 ± 0.02 ppbv yr-1 2σ error)), 5th (0.13 ± 0.02 ppbv yr-1) and 95th (0.16 ± 0.03 ppbv yr-1) percentiles, representative of positive trends in mean, baseline and peak ozone. Assessing the sensitivity of the derived overall trends to the constituent years shows that the European heatwave year of 2003 has significant positive influence and 1998 the converse effect; demonstrating the masking effect of inter-annual variability on decadal based ozone trends. The European scale

  1. Mass and Ozone Fluxes from the Lowermost Stratosphere

    NASA Technical Reports Server (NTRS)

    Schoeberl, Mark R.; Olsen, Mark A.

    2004-01-01

    Net mass flux from the stratosphere to the troposphere can be computed from the heating rate along the 380K isentropic surface and the time rate of change of the mass of the lowermost stratosphere (the region between the tropopause and the 380K isentrope). Given this net mass flux and the cross tropopause diabatic mass flux, the residual adiabatic mass flux across the tropopause can also be estimated. These fluxes have been computed using meteorological fields from a free-running general circulation model (FVGCM) and two assimilation data sets, FVDAS, and UKMO. The data sets tend to agree that the annual average net mass flux for the Northern Hemisphere is about 1P10 kg/s. There is less agreement on the southern Hemisphere flux that might be half as large. For all three data sets, the adiabatic mass flux is computed to be from the upper troposphere into the lowermost stratosphere. This flux will dilute air entering from higher stratospheric altitudes. The mass fluxes are convolved with ozone mixing ratios from the Goddard 3D CTM (which uses the FVGCM) to estimate the cross-tropopause transport of ozone. A relatively large adiabatic flux of tropospheric ozone from the tropical upper troposphere into the extratropical lowermost stratosphere dilutes the stratospheric air in the lowermost stratosphere. Thus, a significant fraction of any measured ozone STE may not be ozone produced in the higher Stratosphere. The results also illustrate that the annual cycle of ozone concentration in the lowermost stratosphere has as much of a role as the transport in the seasonal ozone flux cycle. This implies that a simplified calculation of ozone STE mass from air mass and a mean ozone mixing ratio may have a large uncertainty.

  2. Ozone and cardiovascular injury.

    PubMed

    Srebot, Vera; Gianicolo, Emilio A L; Rainaldi, Giuseppe; Trivella, Maria Giovanna; Sicari, Rosa

    2009-06-24

    Air pollution is increasingly recognized as an important and modifiable determinant of cardiovascular diseases in urban communities. The potential detrimental effects are both acute and chronic having a strong impact on morbidity and mortality. The acute exposure to pollutants has been linked to adverse cardiovascular events such as myocardial infarction, heart failure and life-threatening arrhythmias. The long-terms effects are related to the lifetime risk of death from cardiac causes. The WHO estimates that air pollution is responsible for 3 million premature deaths each year. The evidence supporting these data is very strong nonetheless, epidemiologic and observational data have the main limitation of imprecise measurements. Moreover, the lack of clinical experimental models makes it difficult to demonstrate the individual risk. The other limitation is related to the lack of a clear mechanism explaining the effects of pollution on cardiovascular mortality. In the present review we will explore the epidemiological, clinical and experimental evidence of the effects of ozone on cardiovascular diseases. The pathophysiologic consequences of air pollutant exposures have been extensively investigated in pulmonary systems, and it is clear that some of the major components of air pollution (e.g. ozone and particulate matter) can initiate and exacerbate lung disease in humans 1. It is possible that pulmonary oxidant stress mediated by particulate matter and/or ozone (O3) exposure can result in downstream perturbations in the cardiovasculature, as the pulmonary and cardiovascular systems are intricately associated, and it is well documented that specific environmental toxins (such as tobacco smoke 2) introduced through the lungs can initiate and/or accelerate cardiovascular disease development. Indeed, several epidemiologic studies have proved that there is an association between PM and O3 and the increased incidence of cardiovascular morbidity and mortality 3. Most of the

  3. SAGE II Ozone Analysis

    NASA Technical Reports Server (NTRS)

    Cunnold, Derek; Wang, Ray

    2002-01-01

    Publications from 1999-2002 describing research funded by the SAGE II contract to Dr. Cunnold and Dr. Wang are listed below. Our most recent accomplishments include a detailed analysis of the quality of SAGE II, v6.1, ozone measurements below 20 km altitude (Wang et al., 2002 and Kar et al., 2002) and an analysis of the consistency between SAGE upper stratospheric ozone trends and model predictions with emphasis on hemispheric asymmetry (Li et al., 2001). Abstracts of the 11 papers are attached.

  4. Antarctic total ozone in 1958

    SciTech Connect

    Newman, P.A. )

    1994-04-22

    The Antarctic ozone hole results from catalytic destruction of ozone by chlorine radicals. The hole develops in August, reaches its full depth in early October, and is gone by early December of each year. Extremely low total ozone measurements were made at the Antarctic Dumont d'Urville station in 1958. These measurements were derived from spectrographic plates of the blue sky, the moon, and two stars. These Dumont plate data are inconsistent with 1958 Dobson spectrophotometer ozone measurements, inconsistent with present-day Antarctic observations, and inconsistent with meteorological and theoretical information. There is no credible evidence for an ozone hole in 1958.

  5. Karlson ozone sterilizer. Final report

    SciTech Connect

    Karlson, E.

    1984-05-07

    The authors have a functional sterilization system employing ozone as a sterilization agent. This final report covers the work that led to the first medical sterilizer using ozone as the sterilizing agent. The specifications and the final design were set by hospital operating room personnel and public safety standards. Work on kill tests using bacteria, viruses and fungi determined the necessary time and concentration of ozone necessary for sterilization. These data were used in the Karlson Ozone Sterilizer to determine the length of the steps of the operating cycle and the concentration of ozone to be used. 27 references.

  6. Precision ozone vapor pressure measurements

    NASA Technical Reports Server (NTRS)

    Hanson, D.; Mauersberger, K.

    1985-01-01

    The vapor pressure above liquid ozone has been measured with a high accuracy over a temperature range of 85 to 95 K. At the boiling point of liquid argon (87.3 K) an ozone vapor pressure of 0.0403 Torr was obtained with an accuracy of + or - 0.7 percent. A least square fit of the data provided the Clausius-Clapeyron equation for liquid ozone; a latent heat of 82.7 cal/g was calculated. High-precision vapor pressure data are expected to aid research in atmospheric ozone measurements and in many laboratory ozone studies such as measurements of cross sections and reaction rates.

  7. Normally Expected Aberrations in the 8-hour Dynamic EKG

    NASA Technical Reports Server (NTRS)

    Fleck, R. L.; Arnoldi, L. B.; Townsend, J. C.; Tonesk, X.

    1970-01-01

    The establishment of norms for interpreting long term dynamic electrocardiograms is attempted by correlating a completely disease symptom and cardiac risk factor free sample with a non-pure sample in the direction of normality on various variables. Out of a population of 362 subjects exposed to dynamic electrocardiogram testing, a discrimination between normals and abnormals in terms of traditional risk factors was observed. The two groups differed significantly on the following variables: cholesterol, smoking, systolic blood pressure, white blood count, fasting blood sugar, uric acid, resting EKG, year of birth, and coronary insufficiency.

  8. Validation of OMI total ozone retrievals from the SAO ozone profile algorithm and three operational algorithms with Brewer measurements

    NASA Astrophysics Data System (ADS)

    Bak, J.; Liu, X.; Kim, J. H.; Chance, K.; Haffner, D. P.

    2015-01-01

    The accuracy of total ozone computed from the Smithsonian Astrophysical Observatory (SAO) optimal estimation (OE) ozone profile algorithm (SOE) applied to the Ozone Monitoring Instrument (OMI) is assessed through comparisons with ground-based Brewer spectrometer measurements from 2005 to 2008. We also compare the three OMI operational ozone products, derived from the NASA Total Ozone Mapping Spectrometer (TOMS) algorithm, the KNMI (Royal Netherlands Meteorological Institute) differential optical absorption spectroscopy (DOAS) algorithm, and KNMI's Optimal Estimation (KOE) algorithm. The best agreement is observed between SAO and Brewer, with a mean difference of within 1% at most individual stations. The KNMI OE algorithm systematically overestimates Brewer total ozone by 2% at low and mid-latitudes and 5% at high latitudes while the TOMS and DOAS algorithms underestimate it by ~1.65% on average. Standard deviations of ~1.8% are calculated for both SOE and TOMS, but DOAS and KOE have higher values of 2.2% and 2.6%, respectively. The stability of the SOE algorithm is found to have insignificant dependence on viewing geometry, cloud parameters, or total ozone column. In comparison, the KOE-Brewer differences are significantly correlated with solar and viewing zenith angles and show significant deviations depending on cloud parameters and total ozone amount. The TOMS algorithm exhibits similar stability to SOE with respect to viewing geometry and total column ozone, but has stronger cloud parameter dependence. The dependence of DOAS on observational geometry and geophysical conditions is marginal compared to KOE, but is distinct compared to the SOE and TOMS algorithms. Comparisons of all four OMI products with Brewer show no apparent long-term drift, but seasonal features are evident, especially for KOE and TOMS. The substantial differences in the KOE vs. SOE algorithm performance cannot be sufficiently explained by the use of soft calibration (in SOE) and the use of

  9. Errors in ozone risk assessment using standard conditions for converting ozone concentrations obtained by passive samplers in mountain regions.

    PubMed

    Gerosa, G; Finco, A; Marzuoli, R; Ferretti, M; Gottardini, E

    2012-05-01

    Passive samplers are often employed to measure ozone concentrations in remote areas such as mountain forests. The potential ozone risk for vegetation is then assessed by calculating the AOT40 exposure index (accumulated hourly ozone concentration exceedances above 40 ppb, i.e. AOT40 = Σ([O(3)] - 40)Δt for any hourly ozone concentration [O(3)] > 40 ppb). AOT40 is customary calculated on the basis of ozone concentrations expressed as a volumetric mixing ratio, while lab sheets normally report ozone concentrations from passive samplers in mass units per cubic metre. Concentrations are usually converted from mass units to ppb using a standard conversion factor taking SATP (Standard Ambient Temperature and Pressure) conditions into account. These conditions, however, can vary considerably with elevation. As a consequence, the blanket application of a standard conversion factor may lead to substantial errors in reporting and mapping ozone concentrations and therefore in assessing potential ozone risk in mountain regions. In this paper we carry out a sensitivity analysis of the effects of uncertainties in estimations of air temperature (T) and atmospheric pressure (P) on the concentration conversion factor, and present two examples from two monitoring and mapping exercises carried out in the Italian Alps. We derived P and T at each site from adiabatic lapse rates for temperature and pressure and analysed the magnitude of error in concentration estimations. Results show that the concentration conversion is much more sensitive to uncertainties in P gradient estimation than to air temperature errors. The concentration conversion factor (cf) deviates 5% from the standard transformation at an elevation of 500 m asl. As a consequence, the standard estimated AOT40 at this elevation is about 13% less than the actual value. AOT40 was found to be underestimated by an average between 25% and 34% at typical elevations of mountain forest stands in the Italian Alps when a correct

  10. Ozone and nitrogen dioxide above the northern Tien Shan

    NASA Technical Reports Server (NTRS)

    Arefev, Vladimir N.; Volkovitsky, Oleg A.; Kamenogradsky, Nikita E.; Semyonov, Vladimir K.; Sinyakov, Valery P.

    1994-01-01

    The results of systematic perennial measurements of the total ozone (since 1979) and nitrogen dioxide column (since 1983) in the atmosphere in the European-Asian continent center above the mountainmass of the Tien Shan are given. This region is distinguished by a great number of sunny days during a year. The observation station is at the Northern shore of Issyk Kul Lake (42.56 N 77.04 E 1650 m above the sea level). The measurement results are presented as the monthly averaged atmospheric total ozone and NO2 stratospheric column abundances (morning and evening). The peculiarities of seasonal variations of ozone and nitrogen dioxide atmospheric contents, their regular variances with a quasi-biennial cycles and trends have been noticed. Irregular variances of ozone and nitrogen dioxide atmospheric contents, i.e. their positive and negative anomalies in the monthly averaged contents relative to the perennial averaged monthly means, have been analyzed. The synchronous and opposite in phase anomalies in variations of ozone and nitrogen dioxide atmospheric contents were explained by the transport and zonal circulation in the stratosphere (Kamenogradsky et al., 1990).

  11. Projecting Policy-Relevant Metrics to Characterize Changing Ozone Extremes over the US: Variations by Region, Season and Scenario

    NASA Astrophysics Data System (ADS)

    Rieder, H. E.; Fiore, A. M.; Correa, G. J. P.; Clifton, O.; Horowitz, L. W.; Naik, V.

    2014-12-01

    Nitrogen oxide (NOx) emission controls have led to improved air quality (particularly in the Eastern US) over the past two decades, but concerns have been raised that climate warming may offset some of these gains in the coming decades. Here we address these concerns by analyzing the effect of projected future changes of emissions and climate, in isolation and combination, on US surface ozone (O3) during the 21st century in an ensemble of simulations (3 members per scenario) performed with the GFDL chemistry-climate model CM3. We analyze two Representative Concentration Pathway (RCP) scenarios: RCP4.5 and RCP8.5. Under both scenarios, NOx emissions decrease by ~80% over North America by 2100. In additional 3-member ensemble simulations, termed RCP4.5_WMGG and RCP8.5_WMGG, well-mixed greenhouse gases follow the respective RCP but O3 and aerosol precursor emissions are held at 2005 levels. These simulations enable us to isolate the role of well-mixed greenhouse gas induced climate change from that of emission reductions. Another set of simulations, following RCP8.5 but with methane (CH4) held fixed at 2005 levels, termed RCP8.5_2005CH4, allows us to quantify the background influence of CH4 on O3. For each season, we examine changes in the surface O3 distribution over the US during the 21st century, calculating policy relevant statistics: days above the current national ambient air quality standard (NAAQS) of 75 ppb and other proposed future levels, as well as the probabilistic 1-year return levels for maximum daily 8-hour average ozone (MDA8 O3), within each model grid cell. Specifically, we analyze: (i) regional and seasonal changes in the frequency and return level of high O3 pollution events during the 21st century, as well as (ii) differences among the RCPs by the middle and end of the 21st century. We find that the response of surface O3 to changes in emissions and climate varies strongly, seasonally and spatially, with certain regions more prone to a 'climate

  12. Projecting policy-relevant metrics to characterize changing ozone extremes over the US: Variations by region, season and scenario

    NASA Astrophysics Data System (ADS)

    Rieder, Harald E.; Fiore, Arlene M.; Correa, Gus; Clifton, Olivia; Horrowitz, Larry W.; Naik, Vaishali

    2015-04-01

    Nitrogen oxide (NOx) emission controls have led to improved air quality (particularly in the Eastern US) over the past two decades, but concerns have been raised that climate warming may offset some of these gains in the coming decades. Here we address these concerns by analyzing the effect of projected future changes of emissions and climate, in isolation and combination, on US surface ozone (O3) during the 21st century in an ensemble of simulations (3 members per scenario) performed with the GFDL chemistry-climate model CM3. We analyze two Representative Concentration Pathway (RCP) scenarios: RCP4.5 and RCP8.5. Under both scenarios, NOx emissions decrease by ~80% over North America by 2100. In additional 3-member ensemble simulations, termed RCP4.5_WMGG and RCP8.5_WMGG, well-mixed greenhouse gases follow the respective RCP but O3 and aerosol precursor emissions are held at 2005 levels. These simulations enable us to isolate the role of well-mixed greenhouse gas induced climate change from that of emission reductions. Another set of simulations, following RCP8.5 but with methane (CH4) held fixed at 2005 levels, termed RCP8.5_2005CH4, allows us to quantify the background influence of CH4 on O3. For each season, we examine changes in the surface O3 distribution over the US during the 21st century, calculating policy relevant statistics: days above the current national ambient air quality standard (NAAQS) of 75 ppb and other proposed future levels, as well as the probabilistic 1-year return levels for maximum daily 8-hour average ozone (MDA8 O3), within each model grid cell. Specifically, we analyze: (i) regional and seasonal changes in the frequency and return level of high O3 pollution events during the 21st century, as well as (ii) differences among the RCPs by the middle and end of the 21st century. We find that the response of surface O3 to changes in emissions and climate varies strongly, seasonally and spatially, with certain regions more prone to a 'climate

  13. Surface Ozone and Atmospheric Transport over the Gulf of Maine during ICARTT

    NASA Astrophysics Data System (ADS)

    Hintsa, E.; Twickler, M.; Talbot, R.; Rawlins, T.

    2005-12-01

    As part of the 2004 ICARTT summer campaign, we deployed a buoy with ozone and wind instruments about 20 km ESE of Appledore Island from late June through early September. Data from Thompson Farm, Appledore, and the buoy showed that on average, surface ozone levels over the Gulf of Maine increased with distance from the New Hampshire coast. Diurnally averaged ozone was highest at the buoy site, both in daytime and at night. The diurnal cycle at sea peaked several hours later than at Thompson Farm (3-6 PM EST vs. 1-3 PM). Trajectory and dispersion calculations showed that elevated ozone episodes were generally correlated with air masses from the New York-Boston corridor. The diurnal cycle in ozone at coastal and offshore sites at Martha's Vineyard (about 150 km to the south) was much smaller than in the Gulf of Maine (higher nighttime lows and lower daytime highs), reflecting a higher incidence of marine air at these stations. In summer 2004, the sea-breeze/land-breeze strongly influenced local transport and ozone levels at Appledore and the buoy. For onshore winds, the diurnal cycle in ozone was much smaller than for offshore winds but still present. A weekly cycle in ozone at the Gulf of Maine sites was also observed, with lowest daily ozone maxima on weekends.

  14. TOMS Tropical Tropospheric Ozone Data Sets at the University of Maryland Website

    NASA Technical Reports Server (NTRS)

    Kochhar, A. K.; Thompson, A. M.; Hudson, R. D.; Frolov, A. D.; Witte, J. C.; Einaudi, Franco (Technical Monitor)

    2001-01-01

    Since 1997, shortly after the launch of the Earth-Probe TOMS (Total Ozone Mapping Spectrometer) satellite instrument, we have been processing data in near-real time to post maps of tropical tropospheric ozone at a website: metosrv2.umd.edu/-tropo. Daily, 3-day and 9-day averages of tropical tropospheric ozone column depth (TTO) are viewable from 10N to 10S. Data can be downloaded (running 9-day means) from 20N-30S. Pollution events are trackable along with dynamically-induced variations in tropospheric ozone column. TOMS smoke aerosol (toms.gsfc.nasa.gov) can be used to interpret biomass burning ozone, as for example, during the extreme ozone and smoke pollution period during the ENSO-related fires of August November 1997. During that time plumes of ozone and smoke were frequently decoupled and ozone from Indonesian fires and from Africa merged in one large feature by late October 1997. In addition to the Earth-Probe TOMS record, data as half-month averages and as daily 9-day means from the Nimbus 7 TOMS instrument are at the metosrv2.umd.edu/-tropo website. A guide to the website and examples of ozone time-series and maps will be shown.

  15. Validation of ozone measurements from the Atmospheric Chemistry Experiment (ACE)

    NASA Astrophysics Data System (ADS)

    Dupuy, E.; Walker, K. A.; Kar, J.; Boone, C. D.; McElroy, C. T.; Bernath, P. F.; Drummond, J. R.; Skelton, R.; McLeod, S. D.; Hughes, R. C.; Nowlan, C. R.; Dufour, D. G.; Zou, J.; Nichitiu, F.; Strong, K.; Baron, P.; Bevilacqua, R. M.; Blumenstock, T.; Bodeker, G. E.; Borsdorff, T.; Bourassa, A. E.; Bovensmann, H.; Boyd, I. S.; Bracher, A.; Brogniez, C.; Burrows, J. P.; Catoire, V.; Ceccherini, S.; Chabrillat, S.; Christensen, T.; Coffey, M. T.; Cortesi, U.; Davies, J.; de Clercq, C.; Degenstein, D. A.; de Mazière, M.; Demoulin, P.; Dodion, J.; Firanski, B.; Fischer, H.; Forbes, G.; Froidevaux, L.; Fussen, D.; Gerard, P.; Godin-Beekmann, S.; Goutail, F.; Granville, J.; Griffith, D.; Haley, C. S.; Hannigan, J. W.; Höpfner, M.; Jin, J. J.; Jones, A.; Jones, N. B.; Jucks, K.; Kagawa, A.; Kasai, Y.; Kerzenmacher, T. E.; Kleinböhl, A.; Klekociuk, A. R.; Kramer, I.; Küllmann, H.; Kuttippurath, J.; Kyrölä, E.; Lambert, J.-C.; Livesey, N. J.; Llewellyn, E. J.; Lloyd, N. D.; Mahieu, E.; Manney, G. L.; Marshall, B. T.; McConnell, J. C.; McCormick, M. P.; McDermid, I. S.; McHugh, M.; McLinden, C. A.; Mellqvist, J.; Mizutani, K.; Murayama, Y.; Murtagh, D. P.; Oelhaf, H.; Parrish, A.; Petelina, S. V.; Piccolo, C.; Pommereau, J.-P.; Randall, C. E.; Robert, C.; Roth, C.; Schneider, M.; Senten, C.; Steck, T.; Strandberg, A.; Strawbridge, K. B.; Sussmann, R.; Swart, D. P. J.; Tarasick, D. W.; Taylor, J. R.; Tétard, C.; Thomason, L. W.; Thompson, A. M.; Tully, M. B.; Urban, J.; Vanhellemont, F.; Vigouroux, C.; von Clarmann, T.; von der Gathen, P.; von Savigny, C.; Waters, J. W.; Witte, J. C.; Wolff, M.; Zawodny, J. M.

    2009-01-01

    This paper presents extensive {bias determination} analyses of ozone observations from the Atmospheric Chemistry Experiment (ACE) satellite instruments: the ACE Fourier Transform Spectrometer (ACE-FTS) and the Measurement of Aerosol Extinction in the Stratosphere and Troposphere Retrieved by Occultation (ACE-MAESTRO) instrument. Here we compare the latest ozone data products from ACE-FTS and ACE-MAESTRO with coincident observations from nearly 20 satellite-borne, airborne, balloon-borne and ground-based instruments, by analysing volume mixing ratio profiles and partial column densities. The ACE-FTS version 2.2 Ozone Update product reports more ozone than most correlative measurements from the upper troposphere to the lower mesosphere. At altitude levels from 16 to 44 km, the average values of the mean relative differences are nearly all within +1 to +8%. At higher altitudes (45-60 km), the ACE-FTS ozone amounts are significantly larger than those of the comparison instruments, with mean relative differences of up to +40% (about +20% on average). For the ACE-MAESTRO version 1.2 ozone data product, mean relative differences are within ±10% (average values within ±6%) between 18 and 40 km for both the sunrise and sunset measurements. At higher altitudes ( 35-55 km), systematic biases of opposite sign are found between the ACE-MAESTRO sunrise and sunset observations. While ozone amounts derived from the ACE-MAESTRO sunrise occultation data are often smaller than the coincident observations (with mean relative differences down to -10%), the sunset occultation profiles for ACE-MAESTRO show results that are qualitatively similar to ACE-FTS, indicating a large positive bias (mean relative differences within +10 to +30%) in the 45-55 km altitude range. In contrast, there is no significant systematic difference in bias found for the ACE-FTS sunrise and sunset measurements.

  16. Spatial regression analysis on 32 years of total column ozone data

    NASA Astrophysics Data System (ADS)

    Knibbe, J. S.; van der A, R. J.; de Laat, A. T. J.

    2014-08-01

    Multiple-regression analyses have been performed on 32 years of total ozone column data that was spatially gridded with a 1 × 1.5° resolution. The total ozone data consist of the MSR (Multi Sensor Reanalysis; 1979-2008) and 2 years of assimilated SCIAMACHY (SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY) ozone data (2009-2010). The two-dimensionality in this data set allows us to perform the regressions locally and investigate spatial patterns of regression coefficients and their explanatory power. Seasonal dependencies of ozone on regressors are included in the analysis. A new physically oriented model is developed to parameterize stratospheric ozone. Ozone variations on nonseasonal timescales are parameterized by explanatory variables describing the solar cycle, stratospheric aerosols, the quasi-biennial oscillation (QBO), El Niño-Southern Oscillation (ENSO) and stratospheric alternative halogens which are parameterized by the effective equivalent stratospheric chlorine (EESC). For several explanatory variables, seasonally adjusted versions of these explanatory variables are constructed to account for the difference in their effect on ozone throughout the year. To account for seasonal variation in ozone, explanatory variables describing the polar vortex, geopotential height, potential vorticity and average day length are included. Results of this regression model are compared to that of a similar analysis based on a more commonly applied statistically oriented model. The physically oriented model provides spatial patterns in the regression results for each explanatory variable. The EESC has a significant depleting effect on ozone at mid- and high latitudes, the solar cycle affects ozone positively mostly in the Southern Hemisphere, stratospheric aerosols affect ozone negatively at high northern latitudes, the effect of QBO is positive and negative in the tropics and mid- to high latitudes, respectively, and ENSO affects ozone negatively

  17. Impact of EOS MLS ozone data on medium-extended range ensemble weather forecasts

    NASA Astrophysics Data System (ADS)

    Cheung, J. C. H.; Haigh, J. D.; Jackson, D. R.

    2014-08-01

    As the stratosphere is largely characterized by its ozone abundance, the quality of the ozone field is important for a realistic representation of the stratosphere in weather and climate models. While the stratosphere is directly affected by radiative heating from ozone photodissociation, ozone abundance might also impact the representation of the troposphere since the stratosphere and troposphere are dynamically linked. In this paper, we examine the potential benefits of using ozone data from the Earth Observing System (EOS) Microwave Limb Sounder (MLS) for medium-extended range tropospheric forecasts in a current numerical weather prediction system. The global component of the Met Office Global and Regional Ensemble Prediction System is used, which is run at a resolution of N216 L85 with 24 ensemble members. We compare two scenarios of 31 day forecasts covering the same period, one with the current operational ozone climatology and the other with a monthly mean zonally averaged ozone field computed from the MLS data set. In the extreme case of the Arctic "ozone hole" of March 2011, our results show a general reduction in stratospheric forecast errors in the tropics and Southern Hemisphere as a result of the improved representation of ozone. However, even in such a scenario, where the MLS ozone field is much superior to that of the control, we find that tropospheric forecast errors in the medium-extended range are dominated by the spread of ensemble members and no significant reduction in the root-mean-square forecast errors.

  18. Vertical ozone distributions observed using tethered ozonesondes in a coastal industrial city, Kaohsiung, in southern Taiwan.

    PubMed

    Lin, Ching-Ho; Lai, Chin-Hsing; Wu, Yee-Lin; Lai, Hsin-Chih; Lin, Po-Hsiung

    2007-04-01

    This work presents the vertical distributions of ozone and meteorological parameters observed with tethered ozonesondes and meteorological radiosondes in the lower atmosphere during an ozone episode on March 25-27, 2003, in Kaohsiung City in southern Taiwan. Kaohsiung is a coastal industrial city with inland mountain ranges to the east. Extremely complicated ozone structures were identified that spanned day and night during the experimental period. During afternoons, the lower atmosphere was divided into two stratified air layers with substantially different ozone concentrations. On the episode day (March 26), average ozone concentration in the near-ground layer was 85 ppb and the aloft layer was 140 ppb. A very high ozone peak of 199 ppb measured aloft likely resulted from an elevated large point source. Several no-ozone air layers, distributed throughout 400-750 m, were observed to transport on shore during the night. As well, elevated ozone layers peaking at 60-90 ppb and 90-160 ppb were detected below and above the no-ozone air layers, respectively. These complicated ozone structures were likely formed through titration of plumes from large point sources and the circulations of sea breezes or combined sea-breeze/mountain flows in the study area.

  19. Climate-driven ground-level ozone extreme in the fall over the Southeast United States

    PubMed Central

    Wang, Yuhang

    2016-01-01

    Ground-level ozone is adverse to human and vegetation health. High ground-level ozone concentrations usually occur over the United States in the summer, often referred to as the ozone season. However, observed monthly mean ozone concentrations in the southeastern United States were higher in October than July in 2010. The October ozone average in 2010 reached that of July in the past three decades (1980–2010). Our analysis shows that this extreme October ozone in 2010 over the Southeast is due in part to a dry and warm weather condition, which enhances photochemical production, air stagnation, and fire emissions. Observational evidence and modeling analysis also indicate that another significant contributor is enhanced emissions of biogenic isoprene, a major ozone precursor, from water-stressed plants under a dry and warm condition. The latter finding is corroborated by recent laboratory and field studies. This climate-induced biogenic control also explains the puzzling fact that the two extremes of high October ozone both occurred in the 2000s when anthropogenic emissions were lower than the 1980s and 1990s, in contrast to the observed decreasing trend of July ozone in the region. The occurrences of a drying and warming fall, projected by climate models, will likely lead to more active photochemistry, enhanced biogenic isoprene and fire emissions, an extension of the ozone season from summer to fall, and an increase of secondary organic aerosols in the Southeast, posing challenges to regional air quality management. PMID:27551089

  20. Climate-driven ground-level ozone extreme in the fall over the Southeast United States.

    PubMed

    Zhang, Yuzhong; Wang, Yuhang

    2016-09-01

    Ground-level ozone is adverse to human and vegetation health. High ground-level ozone concentrations usually occur over the United States in the summer, often referred to as the ozone season. However, observed monthly mean ozone concentrations in the southeastern United States were higher in October than July in 2010. The October ozone average in 2010 reached that of July in the past three decades (1980-2010). Our analysis shows that this extreme October ozone in 2010 over the Southeast is due in part to a dry and warm weather condition, which enhances photochemical production, air stagnation, and fire emissions. Observational evidence and modeling analysis also indicate that another significant contributor is enhanced emissions of biogenic isoprene, a major ozone precursor, from water-stressed plants under a dry and warm condition. The latter finding is corroborated by recent laboratory and field studies. This climate-induced biogenic control also explains the puzzling fact that the two extremes of high October ozone both occurred in the 2000s when anthropogenic emissions were lower than the 1980s and 1990s, in contrast to the observed decreasing trend of July ozone in the region. The occurrences of a drying and warming fall, projected by climate models, will likely lead to more active photochemistry, enhanced biogenic isoprene and fire emissions, an extension of the ozone season from summer to fall, and an increase of secondary organic aerosols in the Southeast, posing challenges to regional air quality management.

  1. Light environment alters ozone uptake per net photosynthetic rate in black cherry trees.

    PubMed

    Fredericksen, T S; Kolb, T E; Skelly, J M; Steiner, K C; Joyce, B J; Savage, J E

    1996-05-01

    Foliar ozone uptake rates of different-sized black cherry (Prunus serotina Ehrh.) trees were compared within a deciduous forest and adjacent openings in north-central Pennsylvania during one growing season. Study trees included open-grown seedlings and saplings, forest understory seedlings and saplings, and sunlit and shaded portions of mature canopy tree crowns. Instantaneous ozone uptake rates were highest in high-light environments primarily because of higher stomatal conductances. Low ozone uptake rates of seedlings and saplings in the forest understory could be attributed partially to lower average ambient ozone concentrations compared to the canopy and open environments. Among the tree size and light combinations tested, ozone uptake rates were highest in open-grown seedlings and lowest in forest-grown seedlings. Despite lower ozone uptake rates of foliage in shaded environments, ozone uptake per net photosynthesis of foliage in shaded environments was significantly higher than that of foliage in sunlit environments because of weaker coupling between net photosynthesis and stomatal conductance in shaded environments. The potential for greater ozone injury in shaded environments as a result of greater ozone uptake per net photosynthesis is consistent with previous reports of greater ozone injury in shaded foliage than in sunlit foliage. PMID:14871717

  2. Climate-driven ground-level ozone extreme in the fall over the Southeast United States.

    PubMed

    Zhang, Yuzhong; Wang, Yuhang

    2016-09-01

    Ground-level ozone is adverse to human and vegetation health. High ground-level ozone concentrations usually occur over the United States in the summer, often referred to as the ozone season. However, observed monthly mean ozone concentrations in the southeastern United States were higher in October than July in 2010. The October ozone average in 2010 reached that of July in the past three decades (1980-2010). Our analysis shows that this extreme October ozone in 2010 over the Southeast is due in part to a dry and warm weather condition, which enhances photochemical production, air stagnation, and fire emissions. Observational evidence and modeling analysis also indicate that another significant contributor is enhanced emissions of biogenic isoprene, a major ozone precursor, from water-stressed plants under a dry and warm condition. The latter finding is corroborated by recent laboratory and field studies. This climate-induced biogenic control also explains the puzzling fact that the two extremes of high October ozone both occurred in the 2000s when anthropogenic emissions were lower than the 1980s and 1990s, in contrast to the observed decreasing trend of July ozone in the region. The occurrences of a drying and warming fall, projected by climate models, will likely lead to more active photochemistry, enhanced biogenic isoprene and fire emissions, an extension of the ozone season from summer to fall, and an increase of secondary organic aerosols in the Southeast, posing challenges to regional air quality management. PMID:27551089

  3. Light environment alters ozone uptake per net photosynthetic rate in black cherry trees.

    PubMed

    Fredericksen, T S; Kolb, T E; Skelly, J M; Steiner, K C; Joyce, B J; Savage, J E

    1996-05-01

    Foliar ozone uptake rates of different-sized black cherry (Prunus serotina Ehrh.) trees were compared within a deciduous forest and adjacent openings in north-central Pennsylvania during one growing season. Study trees included open-grown seedlings and saplings, forest understory seedlings and saplings, and sunlit and shaded portions of mature canopy tree crowns. Instantaneous ozone uptake rates were highest in high-light environments primarily because of higher stomatal conductances. Low ozone uptake rates of seedlings and saplings in the forest understory could be attributed partially to lower average ambient ozone concentrations compared to the canopy and open environments. Among the tree size and light combinations tested, ozone uptake rates were highest in open-grown seedlings and lowest in forest-grown seedlings. Despite lower ozone uptake rates of foliage in shaded environments, ozone uptake per net photosynthesis of foliage in shaded environments was significantly higher than that of foliage in sunlit environments because of weaker coupling between net photosynthesis and stomatal conductance in shaded environments. The potential for greater ozone injury in shaded environments as a result of greater ozone uptake per net photosynthesis is consistent with previous reports of greater ozone injury in shaded foliage than in sunlit foliage.

  4. The Ozone Show.

    ERIC Educational Resources Information Center

    Mathieu, Aaron

    2000-01-01

    Uses a talk show activity for a final assessment tool for students to debate about the ozone hole. Students are assessed on five areas: (1) cooperative learning; (2) the written component; (3) content; (4) self-evaluation; and (5) peer evaluation. (SAH)

  5. Ozone and Cavitation Combination

    NASA Astrophysics Data System (ADS)

    Carreon, Ernestina; Traversoni, Leonardo

    2009-09-01

    From laboratory measurements it is well known that the addition of ozone and cavitation enhances the properties of both, understanding for that the ones related to disinfection and carbon removal from waste water. This paper shows modeling of such phenomena that gives some light to the understanding of it and also provides the opportunity to improve the effectiveness of the current procedures.

  6. Dobson ozone spectrophotometer modification.

    NASA Technical Reports Server (NTRS)

    Komhyr, W. D.; Grass, R. D.

    1972-01-01

    Description of a modified version of the Dobson ozone spectrophotometer in which several outdated electronic design features have been replaced by circuitry embodying more modern design concepts. The resulting improvement in performance characteristics has been obtained without changing the principle of operation of the original instrument.

  7. Ozone Layer Educator's Guide.

    ERIC Educational Resources Information Center

    Environmental Protection Agency, Washington, DC.

    This guide has been developed through a collaborative effort involving the U.S. Environmental Protection Agency (EPA), the National Oceanic and Atmospheric Administration (NOAA), and the National Aeronautics and Space Administration (NASA). It is part of an ongoing commitment to ensure that the results of scientific research on ozone depletion are…

  8. Ozone decomposing filter

    DOEpatents

    Simandl, Ronald F.; Brown, John D.; Whinnery, Jr., LeRoy L.

    1999-01-01

    In an improved ozone decomposing air filter carbon fibers are held together with a carbonized binder in a perforated structure. The structure is made by combining rayon fibers with gelatin, forming the mixture in a mold, freeze-drying, and vacuum baking.

  9. Ozone, CFCs and aerosols.

    PubMed

    1989-07-01

    Chlorofluorocarbons (CFCs) are, from the chemist's point of view, unique compounds with very valuable properties. They are inert, cheap and stable. But they also have devastating effects on the environment, destroying the ozone layer and adding to global warming or the greenhouse effect.

  10. Ozone decomposing filter

    SciTech Connect

    Simandl, R.F.; Brown, J.D.; Whinnery, L.L. Jr.

    1999-11-02

    In an improved ozone decomposing air filter carbon fibers are held together with a carbonized binder in a perforated structure. The structure is made by combining rayon fibers with gelatin, forming the mixture in a mold, freeze-drying, and vacuum baking.

  11. Overview of ozone human exposure and health risk analyses used in the U.S. EPA's review of the ozone air quality standard.

    SciTech Connect

    Whitfield, R. G.

    1999-03-04

    This paper presents an overview of the ozone human exposure and health risk analyses developed under sponsorship of the U.S. Environmental Protection Agency (EPA). These analyses are being used in the current review of the national ambient air quality standards (NAAQS) for ozone. The analyses consist of three principal steps: (1) estimating short-term ozone exposure for particular populations (exposure model); (2) estimating population response to exposures or concentrations (exposure-response or concentration-response models); and (3) integrating concentrations or exposure with concentration-response or exposure-response models to produce overall risk estimates (risk model). The exposure model, called the probabilistic NAAQS exposure model for ozone (pNEM/03), incorporates the following factors: hourly ambient ozone concentrations; spatial distribution of concentrations; ventilation state of individuals at time of exposure; and movement of people through various microenvironments (e.g., outdoors, indoors, inside a vehicle) of varying air quality. Exposure estimates are represented by probability distributions. Exposure-response relationships have been developed for several respiratory symptom and lung function health effects, based on the results of controlled human exposure studies. These relationships also are probabilistic and reflect uncertainties associated with sample size and variability of response among subjects. The analyses also provide estimates of excess hospital admissions in the New York City area based on results from an epidemiology study. Overall risk results for selected health endpoints and recently analyzed air quality scenarios associated with alternative 8-hour NAAQS and the current 1-hour standard for outdoor children are used to illustrate application of the methodology.

  12. Impact of greenhouse gases on the Earth's ozone layer

    NASA Astrophysics Data System (ADS)

    Zadorozhny, Alexander

    A numerical 2-D zonally averaged interactive dynamical radiative-photochemical model of the ozonosphere including aerosol physics is used to examine the role of the greenhouse gases CO2 , CH4 , and N2 O in the future long-term changes of the Earth's ozone layer, in particular in its recovery after reduction of anthropogenic discharges of chlorine and bromine compounds into the atmosphere. The model allows calculating self-consistently diabatic circulation, temperature, gaseous composition of the troposphere and stratosphere at latitudes from the South to North Poles, as well as distribution of sulphate aerosol particles and polar stratospheric clouds (PSCs) of types I and II. The scenarios of expected changes of the anthropogenic pollutants for the period from 1980 through 2050 are taken from Climate Change 2001. The processes, which determine the influence of anthropogenic growth of atmospheric abundance of the greenhouse gases on the dynamics of recovery of the Earth's ozone layer, have been studied in details. Expected cooling of the stratosphere caused by increases of greenhouse gases, most importantly CO2 , essentially influences the ozone layer by two ways: through temperature dependencies of the gas phase reaction rates and through enhancement of polar ozone depletion via increased PSC formation. The model calculations show that a weakness in efficiencies of all gas phase catalytic cycles of the ozone destruction due to cooling of the stratosphere is a dominant mechanism of the impact of the greenhouse gases on the ozone layer in Antarctic as well as at the lower latitudes. This mechanism leads to a significant acceleration of the ozone layer recovery here because of the greenhouse gases growth. On the contrary, the mechanism of the impact of the greenhouse gases on the ozone through PSC modification begins to be more effective in Arctic in comparison with the gas phase mechanism in springs after about 2020, which leads to retard the expected recovery of the

  13. Changes in the vertical distribution of ozone over Canada from ozonesondes: 1980-2001

    NASA Astrophysics Data System (ADS)

    Tarasick, D. W.; Fioletov, V. E.; Wardle, D. I.; Kerr, J. B.; Davies, J.

    2005-01-01

    Measurements of the vertical profile of ozone concentration using balloon-borne ECC ozonesondes have been made weekly since 1980 at several sites in Canada (Edmonton, Goose Bay, Churchill, and Resolute), since 1987 at Alert, and since 1992 at Eureka. Previous analyses of ozone trends over Canada have shown strong negative trends in tropospheric ozone. We present here a new analysis of trends in the vertical distribution of ozone with data up to the end of 2001. In addition, more detailed attention is paid to some potential sources of bias: total ozone correction, background current correction, and time-of-launch (diurnal) variation. For the 1980-2001 period the overall linear trends are primarily negative, both in tropospheric and stratospheric ozone. However, when the data for 1991-2001 only are considered, the trends are positive, even in the lower stratosphere. When the time series are compared with previously reported trends (to 1993), it is evident that ozone has rebounded at all levels below about 63 hPa. These differences do not appear to be related to changes in tropopause height, as the average height of the tropopause (as measured over the ozonesonde stations) has not changed over either the 22-year or the 11-year period. Nevertheless, comparison with another dynamical indicator, the wintertime frequency of occurrence of laminae in the ozone profile, suggests that this rebound may be partly a result of small changes in the atmospheric circulation, rather than a recovery of the ozone layer from halocarbon-induced depletion. The long-term trends in average tropospheric ozone concentrations over Canada are similar to corresponding lower stratospheric trends, and tropospheric ozone levels show significant correlation with lower stratospheric ozone amounts.

  14. Electrochemical concentration cell ozone soundings at two sites during the Stratospheric Ozone Intercomparison Campaign

    NASA Astrophysics Data System (ADS)

    Barnes, Robert A.; Torres, Arnold L.

    1995-05-01

    The Stratospheric Ozone Intercomparison Campaign (STOIC) was designed to compare proposed instruments for the Network for the Detection of Stratospheric Change (NDSC) with established measurement techniques. Ground-based measurements were conducted at Table Mountain, California (34.4°N, 117.7°W), and rocket profiles were made at San Nicolas Island, California (33.3°N, 119.5°W). In an effort to estimate site-to-site differences during the intercomparison, daily soundings were made with balloon-borne electrochemical concentration cell (ECC) ozonesondes at the two sites. Comparisons have been made of the mean values for the soundings at each site. The soundings showed small temperature differences between the two sites with the nighttime Table Mountain measurements up to 2°K cooler than the daytime San Nicolas Island temperatures. Day/night temperature corrections based on the emissivity and absorptivity of the thermistors in the balloon instruments can account for these apparent temperature differences. Ozone partial pressure profiles from the ECCs have been used to estimate atmospheric ozone variability during STOIC. Above 20 km, the lowest altitude for the STOIC comparisons, the average data sets from both sites showed standard deviations that were at or below the estimated 5-6% profile-to-profile repeatability for the ozonesondes. This indicates that atmospheric ozone variability was only of the order of a few percent above 20 km during the 2 weeks of the STOIC campaign. Above 20 km the ozone partial pressures over the Table Mountain site averaged 2.0% lower than over San Nicolas Island.

  15. A New ENSO Index Derived from Satellite Measurements of Column Ozone

    NASA Technical Reports Server (NTRS)

    Ziemke, J. R.; Chandra, S.; Oman, L. D.; Bhartia, P. K.

    2010-01-01

    Column Ozone measured in tropical latitudes from Nimbus 7 total ozone mapping spectrometer (TOMS), Earth Probe TOMS, solar backscatter ultraviolet (SBUV), and Aura ozone monitoring instrument (OMI) are used to derive an El Nino-Southern Oscillation (ENSO) index. This index, which covers a time period from 1979 to the present, is defined as the Ozone ENSO Index (OEI) and is the first developed from atmospheric trace gas measurements. The OEI is constructed by first averaging monthly mean column ozone over two broad regions in the western and eastern Pacific and then taking their difference. This differencing yields a self-calibrating ENSO index which is independent of individual instrument calibration offsets and drifts in measurements over the long record. The combined Aura OMI and MLS ozone data confirm that zonal variability in total column ozone in the tropics caused by ENSO events lies almost entirely in the troposphere. As a result, the OEI can be derived directly from total column ozone instead of tropospheric column ozone. For clear-sky ozone measurements a +1K change in Nino 3.4 index corresponds to +2.9 Dobson Unit (DU) change in the OEI, while a +1 hPa change in SOI coincides with a -1.7DU change in the OEI. For ozone measurements under all cloud conditions these numbers are +2.4DU and -1.4 DU, respectively. As an ENSO index based upon ozone, it is potentially useful in evaluating climate models predicting long term changes in ozone and other trace gases.

  16. A new ENSO index derived from satellite measurements of column ozone

    NASA Astrophysics Data System (ADS)

    Ziemke, J. R.; Chandra, S.; Oman, L. D.; Bhartia, P. K.

    2010-04-01

    Column Ozone measured in tropical latitudes from Nimbus 7 total ozone mapping spectrometer (TOMS), Earth Probe TOMS, solar backscatter ultraviolet (SBUV), and Aura ozone monitoring instrument (OMI) are used to derive an El Nino-Southern Oscillation (ENSO) index. This index, which covers a time period from 1979 to the present, is defined as the "Ozone ENSO Index" (OEI) and is the first developed from atmospheric trace gas measurements. The OEI is constructed by first averaging monthly mean column ozone over two broad regions in the western and eastern Pacific and then taking their difference. This differencing yields a self-calibrating ENSO index which is independent of individual instrument calibration offsets and drifts in measurements over the long record. The combined Aura OMI and MLS ozone data confirm that zonal variability in total column ozone in the tropics caused by ENSO events lies almost entirely in the troposphere. As a result, the OEI can be derived directly from total column ozone instead of tropospheric column ozone. For clear-sky ozone measurements a +1 K change in Nino 3.4 index corresponds to +2.9 Dobson Unit (DU) change in the OEI, while a +1 hPa change in SOI coincides with a -1.7 DU change in the OEI. For ozone measurements under all cloud conditions these numbers are +2.4 DU and -1.4 DU, respectively. As an ENSO index based upon ozone, it is potentially useful in evaluating climate models predicting long term changes in ozone and other trace gases.

  17. 16 CFR 260.11 - Ozone-safe and ozone-friendly claims.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... friendly to, the ozone layer or the atmosphere. Example 1: A product is labeled “ozone-friendly.” The claim... 16 Commercial Practices 1 2013-01-01 2013-01-01 false Ozone-safe and ozone-friendly claims. 260.11... THE USE OF ENVIRONMENTAL MARKETING CLAIMS § 260.11 Ozone-safe and ozone-friendly claims. It...

  18. 16 CFR 260.11 - Ozone-safe and ozone-friendly claims.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... friendly to, the ozone layer or the atmosphere. Example 1: A product is labeled “ozone-friendly.” The claim... 16 Commercial Practices 1 2014-01-01 2014-01-01 false Ozone-safe and ozone-friendly claims. 260.11... THE USE OF ENVIRONMENTAL MARKETING CLAIMS § 260.11 Ozone-safe and ozone-friendly claims. It...

  19. Ozone variability over Antarctic continent

    NASA Astrophysics Data System (ADS)

    Concepcion Parrondo, Mā; Yela, Margarita; Gil, Manuel; Ochoa, Hector

    2010-05-01

    Ozonesoundings data from Antarctic Belgrano Station (78°S, 34°W) carried out since 1999 are used to analyze the inter-annual variability of ozone in the troposphere and lower stratosphere. Tropospheric ozone has been calculated integrating the ozone content from the ground up to the ozone tropopause for each ozonesounding using Betan et al. [1996], definition. The annual cycle of the tropospheric ozone values shows an increase from summer to winter months. In August, tropospheric ozone almost doubles the values in February. Dynamical and chemical factors responsible of this behaviour are presented. Ozone loss rate during September in the lower stratosphere for the eleven year record is presented. The highest inter-annual ozone variability in observed during November and December in the lower stratosphere (12-27 km). Minimum ozone values concentration in the 20-27 km layer are found in November 2008. Mean 2008 December 12-20 km partial column remained below 40 DU, lower by 35% than the 2000-2005 mean. We present the relationship between the potential vorticity, timing of the vortex breakup date, the strength of the vortex and ozone concentration at different levels in an attempt to find dynamical features responsible for the observed behavior.

  20. CFCS and the ozone layer.

    PubMed

    Hayman, G D

    1997-05-01

    Ozone is an important constituent of the atmosphere. Ozone forms a distinct layer in the lower stratosphere known as the ozone layer. The ozone layer acts as a fragile shield because it protects man and other life forms from exposure to harmful short-wavelength ultraviolet (UV) radiation. The agents, particularly chemical, which affect the amount of ozone present in the atmosphere have been a source of concern for more than 20 years. This has been reinforced by the dramatic decline of stratospheric ozone levels first measured in Antarctica and now apparent worldwide. The combination of routine measurements of ozone depletion, careful laboratory studies and mathematical modelling of ozone in the atmosphere, has demonstrated that the reactive fragments produced when chlorofluorocarbons (CFCs), halons and other halogenated compounds break down in the stratosphere are responsible for the ozone loss. As CFCs have widespread and sometimes apparently essential uses in modern society, there has been an intense effort to develop safe, effective replacements which have a negligible or much smaller impact on the environment. The Montreal Protocol, signed by over 140 nations, has been implemented to control and phase out the chemical compounds responsible for ozone loss.

  1. Sensitivity of the FVGCM to Changes in Ozone

    NASA Technical Reports Server (NTRS)

    Stolarski; Pawson, S.; Nielsen, J. Eric; Douglass, A.; Newman, P.

    2004-01-01

    We have carried out an experiment with the finite volume general circulation model (FVGCM). This experiment consisted of two different imposed changes in the climatological ozone fields assumed in the radiation code. for conditions with no significant ozone hole. This distribution was obtained from a 50-year simulation of the full stratospheric ozone chemistry, with a time-dependent chlorine loading, done with our off-line chemical transport model (CTM). Three years (1978-1980) of this simulation were averaged to form a monthly, zonal-mean ozone distribution that was used in the 20-year integration of the FVGCM for "unperturbed" conditions. The second 20-year GCM integration included a fully-developed ozone hole. This ozone distribution was from three years, 1998-2000, from the same CTM simulation. The goal of this work is to determine the coupled response of the chemistry and dynamics of the stratosphere. These experiments are the first step in understanding the coupled response. An important initial question concerns the significance of the signals: if 20-year integrations turn out to be too short, the runs will be extended.

  2. Precision ozone calibration system based on vapor pressures of ozone

    NASA Technical Reports Server (NTRS)

    Mauersberger, K.; Hanson, D.; Morton, J.

    1987-01-01

    A precision ozone calibration system for stratospheric research has been developed and evaluated. Vapor pressures above solid ozone are mixed with a carrier gas (N2) to produce stratospheric ozone mixing ratios at total pressures of 1 to cover 20 torr. The uncertainty in the ozone mixing ratios is approximately + or - 1.5 percent, the stability of ozone is + or - 0.3 percent. Experiments to be calibrated may sample the gas mixture over a wide range of flow rates; the maximum throughput of gas with corrections of less than 1 percent to ozone is about 200 torr 1/min. A mass spectrometer system continuously monitors the purity and stability of the N2-O3 gas mixture.

  3. Probabilistic aspects of meteorological and ozone regional ensemble forecasts

    SciTech Connect

    Monache, L D; Hacker, J; Zhou, Y; Deng, X; Stull, R

    2006-03-20

    This study investigates whether probabilistic ozone forecasts from an ensemble can be made with skill; i.e., high verification resolution and reliability. Twenty-eight ozone forecasts were generated over the Lower Fraser Valley, British Columbia, Canada, for the 5-day period 11-15 August 2004, and compared with 1-hour averaged measurements of ozone concentrations at five stations. The forecasts were obtained by driving the CMAQ model with four meteorological forecasts and seven emission scenarios: a control run, {+-} 50% NO{sub x}, {+-} 50% VOC, and {+-} 50% NO{sub x} combined with VOC. Probabilistic forecast quality is verified using relative operating characteristic curves, Talagrand diagrams, and a new reliability index. Results show that both meteorology and emission perturbations are needed to have a skillful probabilistic forecast system--the meteorology perturbation is important to capture the ozone temporal and spatial distribution, and the emission perturbation is needed to span the range of ozone-concentration magnitudes. Emission perturbations are more important than meteorology perturbations for capturing the likelihood of high ozone concentrations. Perturbations involving NO{sub x} resulted in a more skillful probabilistic forecast for the episode analyzed, and therefore the 50% perturbation values appears to span much of the emission uncertainty for this case. All of the ensembles analyzed show a high ozone concentration bias in the Talagrand diagrams, even when the biases from the unperturbed emissions forecasts are removed from all ensemble members. This result indicates nonlinearity in the ensemble, which arises from both ozone chemistry and its interaction with input from particular meteorological models.

  4. [Ozone source apportionment at urban area during a typical photochemical pollution episode in the summer of 2013 in the Yangtze River Delta].

    PubMed

    Li, Hao; Li, Li; Huang, Cheng; An, Jing-yu; Yan, Ru-sha; Huang, Hai-ying; Wang, Yang-jun; Lu, Qing; Wang, Qian; Lou, Sheng-rong; Wang, Hong-li; Zhou, Min; Tao, Shi-kang; Qiao, Li-ping; Chen, Ming-hua

    2015-01-01

    With the fast development of urbanization, industrialization and mobilization, the air pollutant emissions with photochemical reactivity become more obvious, causing a severe photochemical pollution with the characteristics of high ozone concentration. However, the ozone source identification is very complicated due to the high non linearity between ozone and its precursors. Thus, ways to reduce ozone is still not clear. A high ozone pollution episode occurred during July, 2013, which lasted for a long period, with large influence area and high intensity. In this paper, we selected this episode to do a case study with the application of ozone source apportionment technology(OSAT) coupled within the CAMx air quality model. In this study, 4 source regions(including Shanghai, north Zhejiang, South Jiangsu and long range transport), 7 source categories (including power plants, industrial process, industrial boilers and kilns, residential, mobile source, volatile source and biogenic emissions) are analyzed to study their contributions to surface O3 in Shanghai, Suzhou and Zhejiang. Results indicate that long range transport contribution to the surface ozone in the YRD is around 20 x 10(-9) - 40 x 10(-9) (volume fraction). The O3 concentrations can increased to 40 x 10(-9) - 100 x 10(-9) (volume fraction) due to precursors emissions in Shanghai, Jiangsu and Zhejiang. As for the regional contribution to 8 hour ozone, long range transport constitutes 42.79% +/- 10.17%, 48.57% +/- 9.97% and 60.13% +/- 7.11% of the surface ozone in Shanghai, Suzhou and Hangzhou, respectively. Regarding the high O3 in Shanghai, local contribution is 28.94% +/- 8.49%, north Zhejiang constitutes 19.83% +/- 10.55%. As for surface O3 in Suzhou, the contribution from south Jiangsu is 26.41% +/- 6.80%. Regarding the surface O3 in Hangzhou, the major regional contributor is north Zhejiang (29.56% +/- 8.33%). Contributions from the long range transport to the daily maximum O3 concentrations are

  5. [Ozone source apportionment at urban area during a typical photochemical pollution episode in the summer of 2013 in the Yangtze River Delta].

    PubMed

    Li, Hao; Li, Li; Huang, Cheng; An, Jing-yu; Yan, Ru-sha; Huang, Hai-ying; Wang, Yang-jun; Lu, Qing; Wang, Qian; Lou, Sheng-rong; Wang, Hong-li; Zhou, Min; Tao, Shi-kang; Qiao, Li-ping; Chen, Ming-hua

    2015-01-01

    With the fast development of urbanization, industrialization and mobilization, the air pollutant emissions with photochemical reactivity become more obvious, causing a severe photochemical pollution with the characteristics of high ozone concentration. However, the ozone source identification is very complicated due to the high non linearity between ozone and its precursors. Thus, ways to reduce ozone is still not clear. A high ozone pollution episode occurred during July, 2013, which lasted for a long period, with large influence area and high intensity. In this paper, we selected this episode to do a case study with the application of ozone source apportionment technology(OSAT) coupled within the CAMx air quality model. In this study, 4 source regions(including Shanghai, north Zhejiang, South Jiangsu and long range transport), 7 source categories (including power plants, industrial process, industrial boilers and kilns, residential, mobile source, volatile source and biogenic emissions) are analyzed to study their contributions to surface O3 in Shanghai, Suzhou and Zhejiang. Results indicate that long range transport contribution to the surface ozone in the YRD is around 20 x 10(-9) - 40 x 10(-9) (volume fraction). The O3 concentrations can increased to 40 x 10(-9) - 100 x 10(-9) (volume fraction) due to precursors emissions in Shanghai, Jiangsu and Zhejiang. As for the regional contribution to 8 hour ozone, long range transport constitutes 42.79% +/- 10.17%, 48.57% +/- 9.97% and 60.13% +/- 7.11% of the surface ozone in Shanghai, Suzhou and Hangzhou, respectively. Regarding the high O3 in Shanghai, local contribution is 28.94% +/- 8.49%, north Zhejiang constitutes 19.83% +/- 10.55%. As for surface O3 in Suzhou, the contribution from south Jiangsu is 26.41% +/- 6.80%. Regarding the surface O3 in Hangzhou, the major regional contributor is north Zhejiang (29.56% +/- 8.33%). Contributions from the long range transport to the daily maximum O3 concentrations are

  6. Balloonborne ozone and aerosol measurements in the antarctic ozone hole

    SciTech Connect

    Hofmann, D.J.; Harder, J.W.; Rolf, S.R.; Rosen, J.M. )

    1987-01-01

    The National Ozone Expedition (NOZE) was mounted in 1986 using winter fly-in flights to McMurdo Station in August, which is approximately the time the ozone reduction begins. The University of Wyoming Atmospheric Physics group participated in this expedition through balloonborne measurements of the vertical distribution of ozone and aerosol particles. Between 24 August and 6 November, 33 ozone soundings, 6 aerosol sounding, and 3 condensation nuclei soundings were conducted using polyethylene balloons which were able to penetrate the cold (< {minus}80C) antarctic stratosphere. The authors summarize these results here.

  7. Ozone and ozone byproducts in the cabins of commercial aircraft.

    PubMed

    Weisel, Clifford; Weschler, Charles J; Mohan, Kris; Vallarino, Jose; Spengler, John D

    2013-05-01

    The aircraft cabin represents a unique indoor environment due to its high surface-to-volume ratio, high occupant density, and the potential for high ozone concentrations at cruising altitudes. Ozone was continuously measured and air was sampled on sorbent traps, targeting carbonyl compounds, on 52 transcontinental U.S. or international flights between 2008 and 2010. The sampling was predominantly on planes that did not have ozone scrubbers (catalytic converters). Peak ozone levels on aircraft without catalytic convertors exceeded 100 ppb, with some flights having periods of more than an hour when the ozone levels were >75 ppb. Ozone was greatly reduced on relatively new aircraft with catalytic convertors, but ozone levels on two flights whose aircraft had older convertors were similar to those on planes without catalytic convertors. Hexanal, heptanal, octanal, nonanal, decanal, and 6-methyl-5-hepten-2-one (6-MHO) were detected in the aircraft cabin at sub- to low ppb levels. Linear regression models that included the log transformed mean ozone concentration, percent occupancy, and plane type were statistically significant and explained between 18 and 25% of the variance in the mixing ratio of these carbonyls. Occupancy was also a significant factor for 6-MHO, but not the linear aldehydes, consistent with 6-MHO's formation from the reaction between ozone and squalene, which is present in human skin oils. PMID:23517299

  8. Fundamental differences between Arctic and Antarctic ozone depletion.

    PubMed

    Solomon, Susan; Haskins, Jessica; Ivy, Diane J; Min, Flora

    2014-04-29

    Antarctic ozone depletion is associated with enhanced chlorine from anthropogenic chlorofluorocarbons and heterogeneous chemistry under cold conditions. The deep Antarctic "hole" contrasts with the generally weaker depletions observed in the warmer Arctic. An unusually cold Arctic stratospheric season occurred in 2011, raising the question of how the Arctic ozone chemistry in that year compares with others. We show that the averaged depletions near 20 km across the cold part of each pole are deeper in Antarctica than in the Arctic for all years, although 2011 Arctic values do rival those seen in less-depleted years in Antarctica. We focus not only on averages but also on extremes, to address whether or not Arctic ozone depletion can be as extreme as that observed in the Antarctic. This information provides unique insights into the contrasts between Arctic and Antarctic ozone chemistry. We show that extreme Antarctic ozone minima fall to or below 0.1 parts per million by volume (ppmv) at 18 and 20 km (about 70 and 50 mbar) whereas the lowest Arctic ozone values are about 0.5 ppmv at these altitudes. At a higher altitude of 24 km (30-mbar level), no Arctic data below about 2 ppmv have been observed, including in 2011, in contrast to values more than an order of magnitude lower in Antarctica. The data show that the lowest ozone values are associated with temperatures below -80 °C to -85 °C depending upon altitude, and are closely associated with reduced gaseous nitric acid concentrations due to uptake and/or sedimentation in polar stratospheric cloud particles. PMID:24733920

  9. Fundamental differences between Arctic and Antarctic ozone depletion

    PubMed Central

    Solomon, Susan; Haskins, Jessica; Ivy, Diane J.; Min, Flora

    2014-01-01

    Antarctic ozone depletion is associated with enhanced chlorine from anthropogenic chlorofluorocarbons and heterogeneous chemistry under cold conditions. The deep Antarctic “hole” contrasts with the generally weaker depletions observed in the warmer Arctic. An unusually cold Arctic stratospheric season occurred in 2011, raising the question of how the Arctic ozone chemistry in that year compares with others. We show that the averaged depletions near 20 km across the cold part of each pole are deeper in Antarctica than in the Arctic for all years, although 2011 Arctic values do rival those seen in less-depleted years in Antarctica. We focus not only on averages but also on extremes, to address whether or not Arctic ozone depletion can be as extreme as that observed in the Antarctic. This information provides unique insights into the contrasts between Arctic and Antarctic ozone chemistry. We show that extreme Antarctic ozone minima fall to or below 0.1 parts per million by volume (ppmv) at 18 and 20 km (about 70 and 50 mbar) whereas the lowest Arctic ozone values are about 0.5 ppmv at these altitudes. At a higher altitude of 24 km (30-mbar level), no Arctic data below about 2 ppmv have been observed, including in 2011, in contrast to values more than an order of magnitude lower in Antarctica. The data show that the lowest ozone values are associated with temperatures below −80 °C to −85 °C depending upon altitude, and are closely associated with reduced gaseous nitric acid concentrations due to uptake and/or sedimentation in polar stratospheric cloud particles. PMID:24733920

  10. Fundamental differences between Arctic and Antarctic ozone depletion.

    PubMed

    Solomon, Susan; Haskins, Jessica; Ivy, Diane J; Min, Flora

    2014-04-29

    Antarctic ozone depletion is associated with enhanced chlorine from anthropogenic chlorofluorocarbons and heterogeneous chemistry under cold conditions. The deep Antarctic "hole" contrasts with the generally weaker depletions observed in the warmer Arctic. An unusually cold Arctic stratospheric season occurred in 2011, raising the question of how the Arctic ozone chemistry in that year compares with others. We show that the averaged depletions near 20 km across the cold part of each pole are deeper in Antarctica than in the Arctic for all years, although 2011 Arctic values do rival those seen in less-depleted years in Antarctica. We focus not only on averages but also on extremes, to address whether or not Arctic ozone depletion can be as extreme as that observed in the Antarctic. This information provides unique insights into the contrasts between Arctic and Antarctic ozone chemistry. We show that extreme Antarctic ozone minima fall to or below 0.1 parts per million by volume (ppmv) at 18 and 20 km (about 70 and 50 mbar) whereas the lowest Arctic ozone values are about 0.5 ppmv at these altitudes. At a higher altitude of 24 km (30-mbar level), no Arctic data below about 2 ppmv have been observed, including in 2011, in contrast to values more than an order of magnitude lower in Antarctica. The data show that the lowest ozone values are associated with temperatures below -80 °C to -85 °C depending upon altitude, and are closely associated with reduced gaseous nitric acid concentrations due to uptake and/or sedimentation in polar stratospheric cloud particles.

  11. Comparison of modelled and measured ozone concentrations and meteorology for a site in south-west Sweden: implications for ozone uptake calculations.

    PubMed

    Klingberg, Jenny; Danielsson, Helena; Simpson, David; Pleijel, Håkan

    2008-09-01

    Measurements of ground-level ozone concentrations and meteorology (temperature, vapour pressure deficit (VPD), solar radiation) at the monitoring site Ostad (south-west Sweden) were compared to data from the corresponding grid in the EMEP photo-oxidant model for 1997, 1999 and 2000. The influence of synoptic weather on the agreement between model and measurements was studied. Implications of differences between modelled and observed inputs for ozone flux calculations for wheat and potato were investigated. The EMEP model output of ozone, temperature and VPD correlated well with measurements during daytime. Deviations were larger during the night, especially in calm conditions, attributed to local climatological conditions at the monitoring site deviating from average conditions of the grid. These differences did not lead to significant differences in calculated ozone uptake, which was reproduced remarkably well. The uptake calculations were sensitive to errors in the ozone and temperature input data, especially when including a flux threshold.

  12. Factors influencing the ground level distribution of ozone in Europe.

    PubMed

    Derwent, R G; Kay, P J

    1988-01-01

    Ozone is a widely distributed pollutant in the atmospheric boundary layer over north west Europe. Three main sources have been identified: the stratosphere, the free troposphere and boundary layer photochemical production. The pattern of ground level ozone concentrations resulting from these three sources cannot be accurately specified. Ozone shows significant variations in space and time but because of the high cost of continuous monitoring equipment, spatial variations on a national and international basis have not been studied in detail. Variations in ozone concentrations at individual monitoring sites have been given a great deal of attention and experience gained from United Kingdom monitoring sites is described in some detail. The averaging time statistical model of Larsen is employed to relate the exposure levels measured over different averaging periods. Diurnal variations have a major influence on exposure levels at sites nominally exposed to the same regional ozone distribution. The physical and chemical mechanisms which give rise to diurnal variations are detailed so that sites can be screened for different diurnal behaviour characteristics.

  13. Degradation of carbofuran by ozonation.

    PubMed

    Suneethi, S; Joseph, Kurian

    2009-04-01

    Degradation of commercial grade carbofuran (2, 3 dihydro-2, 2-dimethyl-7 benzo furanyl-N-methyl carbamate) in aqueous solution by ozone oxidation was investigated using bench scale experiments. The degradation rate was strongly influenced by the ozone dosage, pH, initial concentration of carbofuran and contact time of ozonation. Carbofuran solution of 200ppm concentration was degraded by 79% within 10 minutes consuming 87 mg of ozone at pH 4. The associated TOC reduction was observed to be 53%. Ammonium (20 mg/L) and nitrate (30 mg/L) ions were detected in the effluent as degradation products of ozonation. The results support the effectiveness of ozonation for degradation of organic pesticides such as carbofuran.

  14. Ozone Risk Assessment Utilities

    1999-08-10

    ORAMUS is a user-friendly, menu-driven software system that calculates and displays user-selected risk estimates for health effects attributable to short-term exposure to tropospheric ozone. Inputs to the risk assessment are estimates of exposure to ozone and exposure-response relationships to produce overall risk estimates in the form of probability distributions. Three fundamental models are included: headcount risk, benchmark risk, and hospital admissions. Exposure-response relationships are based on results of controlled human exposure studies. Exposure estimates aremore » based on the EPA''s probabilistic national ambient air quality standards (NAAQS) exposure model, pNEM/Osub3, which simulates air quality associated with attainment of alternative NAAQS. Using ORAMUS, risk results for 27 air quality scenarios, air quality in 9 urban areas, 33 health endpoints, and 4 chronic health endpoints can be calculated.« less

  15. Ozonated olive oils and the troubles.

    PubMed

    Uysal, Bulent

    2014-01-01

    One of the commonly used methods for ozone therapy is ozonated oils. Most prominent type of used oils is extra virgin olive oil. But still, each type of unsaturated oils may be used for ozonation. There are a lot of wrong knowledge on the internet about ozonated oils and its use as well. Just like other ozone therapy studies, also the studies about ozone oils are inadequate to avoid incorrect knowledge. Current data about ozone oil and its benefits are produced by supplier who oversees financial interests and make misinformation. Despite the rapidly increasing ozone oil sales through the internet, its quality and efficacy is still controversial. Dozens of companies and web sites may be easily found to buy ozonated oil. But, very few of these products are reliable, and contain sufficiently ozonated oil. This article aimed to introduce the troubles about ozonated oils and so to inform ozonated oil users. PMID:26401346

  16. Ozone, Air Quality, and Asthma (For Parents)

    MedlinePlus

    ... found in both the Earth's upper and lower atmospheres. The protective ozone in the upper atmosphere is very different from the harmful ozone in the lower atmosphere. Ozone that exists naturally 10 to 30 miles ( ...

  17. A Novel Gene, OZONE-RESPONSIVE APOPLASTIC PROTEIN1, Enhances Cell Death in Ozone Stress in Rice.

    PubMed

    Ueda, Yoshiaki; Siddique, Shahid; Frei, Michael

    2015-09-01

    A novel protein, OZONE-RESPONSIVE APOPLASTIC PROTEIN1 (OsORAP1), was characterized, which was previously suggested as a candidate gene underlying OzT9, a quantitative trait locus for ozone stress tolerance in rice (Oryza sativa). The sequence of OsORAP1 was similar to that of ASCORBATE OXIDASE (AO) proteins. It was localized in the apoplast, as shown by transient expression of an OsORAP1/green fluorescent protein fusion construct in Nicotiana benthamiana leaf epidermal and mesophyll cells, but did not possess AO activity, as shown by heterologous expression of OsORAP1 in Arabidopsis (Arabidopsis thaliana) mutants with reduced background AO activity. A knockout rice line of OsORAP1 showed enhanced tolerance to ozone stress (120 nL L(-1) average daytime concentration, 20 d), as demonstrated by less formation of leaf visible symptoms (i.e. cell death), less lipid peroxidation, and lower NADPH oxidase activity, indicating reduced active production of reactive oxygen species. In contrast, the effect of ozone on chlorophyll content was not significantly different among the lines. These observations suggested that OsORAP1 specifically induced cell death in ozone stress. Significantly enhanced expression of jasmonic acid-responsive genes in the knockout line implied the involvement of the jasmonic acid pathway in symptom mitigation. Sequence analysis revealed extensive polymorphisms in the promoter region of OsORAP1 between the ozone-susceptible cv Nipponbare and the ozone-tolerant cv Kasalath, the OzT9 donor variety, which could be responsible for the differential regulation of OsORAP1 reported earlier. These pieces of evidence suggested that OsORAP1 enhanced cell death in ozone stress, and its expression levels could explain the effect of a previously reported quantitative trait locus.

  18. A Novel Gene, OZONE-RESPONSIVE APOPLASTIC PROTEIN1, Enhances Cell Death in Ozone Stress in Rice1

    PubMed Central

    Ueda, Yoshiaki; Siddique, Shahid; Frei, Michael

    2015-01-01

    A novel protein, OZONE-RESPONSIVE APOPLASTIC PROTEIN1 (OsORAP1), was characterized, which was previously suggested as a candidate gene underlying OzT9, a quantitative trait locus for ozone stress tolerance in rice (Oryza sativa). The sequence of OsORAP1 was similar to that of ASCORBATE OXIDASE (AO) proteins. It was localized in the apoplast, as shown by transient expression of an OsORAP1/green fluorescent protein fusion construct in Nicotiana benthamiana leaf epidermal and mesophyll cells, but did not possess AO activity, as shown by heterologous expression of OsORAP1 in Arabidopsis (Arabidopsis thaliana) mutants with reduced background AO activity. A knockout rice line of OsORAP1 showed enhanced tolerance to ozone stress (120 nL L−1 average daytime concentration, 20 d), as demonstrated by less formation of leaf visible symptoms (i.e. cell death), less lipid peroxidation, and lower NADPH oxidase activity, indicating reduced active production of reactive oxygen species. In contrast, the effect of ozone on chlorophyll content was not significantly different among the lines. These observations suggested that OsORAP1 specifically induced cell death in ozone stress. Significantly enhanced expression of jasmonic acid-responsive genes in the knockout line implied the involvement of the jasmonic acid pathway in symptom mitigation. Sequence analysis revealed extensive polymorphisms in the promoter region of OsORAP1 between the ozone-susceptible cv Nipponbare and the ozone-tolerant cv Kasalath, the OzT9 donor variety, which could be responsible for the differential regulation of OsORAP1 reported earlier. These pieces of evidence suggested that OsORAP1 enhanced cell death in ozone stress, and its expression levels could explain the effect of a previously reported quantitative trait locus. PMID:26220952

  19. A Transport Analysis of In Situ Airborne Ozone Measurements from the 2011 DISCOVER-AQ Campaign

    NASA Astrophysics Data System (ADS)

    Arkinson, H. L.; Brent, L. C.; He, H.; Loughner, C.; Stehr, J. W.; Weinheimer, A. J.; Dickerson, R. R.

    2013-12-01

    Baltimore and Washington are currently designated as nonattainment areas with respect to the 2008 EPA National Ambient Air Quality Standard (NAAQS) for 8-hour Ozone (O3). Tropospheric O3 is the dominant component of summertime photochemical smog, and at high levels, has deleterious effects on human health, ecosystems, and materials. The University of Maryland (UMD) Regional Atmospheric Measurement Modeling and Prediction Program (RAMMPP) strives to improve understanding of air quality in the Mid-Atlantic States and to elucidate contributions of pollutants such as O3 from regional transport versus local sources through a combination of modeling and in situ measurements. The NASA Deriving Information on Surface Conditions from Column and Vertically Resolved Observations Relevant to Air Quality (DISCOVER-AQ) project investigates the connection between column measurements and surface conditions to explore the potential of remote sensing observations in diagnosing air quality at ground level where pollutants can affect human health. During the 2011 DISCOVER-AQ field campaign, in situ airborne measurements of trace gases and aerosols were performed along the Interstate 95 corridor between Baltimore and Washington from the NASA P3B aircraft. To augment this data and provide regional context, measurements of trace gases and aerosols were also performed by the RAMMPP Cessna 402B aircraft over nearby airports in Maryland and Virginia. This work presents an analysis of O3 measurements made by the Ultraviolet (UV) Photometric Ambient O3 Analyzer on the RAMMPP Cessna 402B and by the NCAR 4-Channel Chemiluminescence instrument on the NASA P3B. In this analysis, spatial and temporal patterns of O3 data are examined within the context of forward and backward trajectories calculated from 12-km North American Mesoscale (NAM) meteorological data using the NOAA Hybrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT) Model and from a high resolution Weather Research and

  20. Springtime high surface ozone events over the western United States: Quantifying the role of stratospheric intrusions

    NASA Astrophysics Data System (ADS)

    Fiore, A. M.; Lin, M.; Cooper, O. R.; Horowitz, L. W.; Naik, V.; Levy, H.; Langford, A. O.; Johnson, B. J.; Oltmans, S. J.; Senff, C. J.

    2011-12-01

    As the National Ambient Air Quality (NAAQS) standard for ozone (O_{3}) is lowered, it pushes closer to policy-relevant background levels (O_{3} concentrations that would exist in the absence of North American anthropogenic emissions), making attainment more difficult with local controls. We quantify the Asian and stratospheric components of this North American background, with a primary focus on the western United States. Prior work has identified this region as a hotspot for deep stratospheric intrusions in spring. We conduct global simulations at 200 km and 50 km horizontal resolution with the GFDL AM3 model, including a stratospheric O_{3} tracer and two sensitivity simulations with anthropogenic emissions from Asia and North America turned off. The model is evaluated with a suite of in situ and satellite measurements during the NOAA CalNex campaign (May-June 2010). The model reproduces the principle features in the observed surface to near tropopause distribution of O_{3} along the California coast, including its latitudinal variation and the development of regional high-O_{3} episodes. Four deep tropopause folds are diagnosed and we find that the remnants of these stratospheric intrusions are transported to the surface of Southern California and Western U.S. Rocky Mountains, contributing 10-30 ppbv positive anomalies relative to the simulated campaign mean stratospheric component in the model surface layer. We further examine the contribution of North American background, including its stratospheric and Asian components, to the entire distribution of observed MDA8 O_{3} at 12 high-elevation CASTNet sites in the Mountain West. We find that the stratospheric O_{3} tracer constitutes 50% of the North American background, and can enhance surface maximum daily 8-hour average (MDA8) O_{3} by 20 ppb when observed surface O_{3} is in the range of 60-80 ppbv. Our analysis highlights the potential for natural sources such as deep stratospheric intrusions to contribute

  1. Protecting the ozone layer.

    PubMed

    Munasinghe, M; King, K

    1992-06-01

    Stratospheric ozone layer depletion has been recognized as a problem by the Vienna Convention for the Protection of the Ozone Layer and the 1987 Montreal Protocol (MP). The ozone layer shields the earth from harmful ultraviolet radiation (UV-B), which is more pronounced at the poles and around the equator. Industrialized countries have contributed significantly to the problem by releasing chlorofluorocarbons (CFCs) and halons into the atmosphere. The effect of these chemicals, which were known for their inertness, nonflammability, and nontoxicity, was discovered in 1874. Action to deal with the effects of CFCs and halons was initiated in 1985 in a 49-nation UN meeting. 21 nations signed a protocol limiting ozone depleting substances (ODS): CFCs and halons. Schedules were set based on each country's use in 1986; the target phaseout was set for the year 2000. The MP restricts trade in ODSs and weights the impact of substances to reflect the extent of damage; i.e., halons are 10 times more damaging than CFCs. ODS requirements for developing countries were eased to accommodate scarce resources and the small fraction of ODS emissions. An Interim Multilateral Fund under the Montreal Protocol (IMFMP) was established to provide loans to finance the costs to developing countries in meeting global environmental requirements. The IMFMP is administered by the World Bank, the UN Environmental Program, and the UN Development Program. Financing is available to eligible countries who use .3 kg of ODS/person/year. Rapid phaseout in developed countries has occurred due to strong support from industry and a lower than expected cost. Although there are clear advantages to rapid phaseout, there were no incentives included in the MP for rapid phaseout. Some of the difficulties occur because the schedules set minimum targets at the lowest possible cost. Also, costs cannot be minimized by a country-specific and ODS-specific process. The ways to improve implementation in scheduling and

  2. Ozone attainment: A different perspective

    SciTech Connect

    Beck, W.B. )

    1988-01-01

    Recent attention on the ozone non-attainment issue has been focused on Washington. Both Congress and the EPA have made efforts at addressing the post-1987 crisis in the many non-attainment areas. In contrast to the political activity, this paper presents some interesting technical perspectives on ozone attainment for many areas of the U.S.. Issues such as transport, climate and natural ozone sources are discussed in the context of exceedance frequency for several geographical areas of the country.

  3. Multimodel projections of stratospheric ozone in the 21st century

    NASA Astrophysics Data System (ADS)

    Eyring, V.; Waugh, D. W.; Bodeker, G. E.; Cordero, E.; Akiyoshi, H.; Austin, J.; Beagley, S. R.; Boville, B. A.; Braesicke, P.; Brühl, C.; Butchart, N.; Chipperfield, M. P.; Dameris, M.; Deckert, R.; Deushi, M.; Frith, S. M.; Garcia, R. R.; Gettelman, A.; Giorgetta, M. A.; Kinnison, D. E.; Mancini, E.; Manzini, E.; Marsh, D. R.; Matthes, S.; Nagashima, T.; Newman, P. A.; Nielsen, J. E.; Pawson, S.; Pitari, G.; Plummer, D. A.; Rozanov, E.; Schraner, M.; Scinocca, J. F.; Semeniuk, K.; Shepherd, T. G.; Shibata, K.; Steil, B.; Stolarski, R. S.; Tian, W.; Yoshiki, M.

    2007-08-01

    Simulations from eleven coupled chemistry-climate models (CCMs) employing nearly identical forcings have been used to project the evolution of stratospheric ozone throughout the 21st century. The model-to-model agreement in projected temperature trends is good, and all CCMs predict continued, global mean cooling of the stratosphere over the next 5 decades, increasing from around 0.25 K/decade at 50 hPa to around 1 K/decade at 1 hPa under the Intergovernmental Panel on Climate Change (IPCC) Special Report on Emissions Scenarios (SRES) A1B scenario. In general, the simulated ozone evolution is mainly determined by decreases in halogen concentrations and continued cooling of the global stratosphere due to increases in greenhouse gases (GHGs). Column ozone is projected to increase as stratospheric halogen concentrations return to 1980s levels. Because of ozone increases in the middle and upper stratosphere due to GHG-induced cooling, total ozone averaged over midlatitudes, outside the polar regions, and globally, is projected to increase to 1980 values between 2035 and 2050 and before lower-stratospheric halogen amounts decrease to 1980 values. In the polar regions the CCMs simulate small temperature trends in the first and second half of the 21st century in midwinter. Differences in stratospheric inorganic chlorine (Cly) among the CCMs are key to diagnosing the intermodel differences in simulated ozone recovery, in particular in the Antarctic. It is found that there are substantial quantitative differences in the simulated Cly, with the October mean Antarctic Cly peak value varying from less than 2 ppb to over 3.5 ppb in the CCMs, and the date at which the Cly returns to 1980 values varying from before 2030 to after 2050. There is a similar variation in the timing of recovery of Antarctic springtime column ozone back to 1980 values. As most models underestimate peak Cly near 2000, ozone recovery in the Antarctic could occur even later, between 2060 and 2070. In the

  4. Assessment of SAGE Version 6.1 Ozone Data Quality

    NASA Technical Reports Server (NTRS)

    Wang, Hsiang J.; Cunnold, Derek M.; Thomason, Larry W.; Zawodny, Joseph M.; Bodeker, Greg E.

    2002-01-01

    The SAGE-II V6.1 ozone retrievals are shown to be of better precision at all levels and to be much more accurate than previous retrievals in the lower stratosphere below 20 km altitude. A filtering procedure for removing anomalous ozone profiles associated with volcanic aerosol/cloud effects and other identified artifacts in V6.1 ozone is described. The agreement between SAGE and ozonesondes in the mean is shown to be approximately 10% down to the tropopause. Relative to the sondes SAGE tends to slightly overestimate ozone (less than 5%) between 15 and 20 km altitude, and systematically underestimates ozone in the troposphere by approximately 30% in the regions between 8 km altitude and 2 km below the tropopause. The precisions (random errors) of SAGE ozone retrievals above 25 km altitude are estimated to be 4% or better; they are a factor of ten worse below 16 km altitude. Linear trends in the differences between coincident SAGE and ozonesondes measurement are generally less than 0.3 %/year and not significantly different from zero in 95% confidence intervals. Compared to V5.96 retrievals, ozone trend differences between 20 and 50 km altitude are approximately 0. 1 %/year, below 20 km altitude the SAGE II trends are more positive by approximately 0.2 %/year. For the 1984-1999 period the SAGE-II shows a localized ozone loss of -0.4(+/- 0.25) %/year (2gigma) in the tropics at 20 km altitude. In the lower stratosphere between 16 and 22 km altitudes, the SAGE shows significant ozone losses in the mid-latitudes in both Hemispheres during the 1979-1999 periods. The ozone trends range from -0.24(+/- 0.18) to -0.77(+/- 0.46) (2sigma)%/year. However in the 1984-1999 period, the downward trends are smaller (-0.07 to - 0.25 %/year) in this altitude range, and the trends in the integrated column from 12 to 17 km altitude in mid-latitudes (35 deg - 60 deg) are not significantly different from zero (0.1 +?- 0.6 (2sigma)%/year). Averaged over the tropics (20 deg S to 20 deg N

  5. Improvements in Total Column Ozone in GEOSCCM and Comparisons with a New Ozone-Depleting Substances Scenario

    NASA Technical Reports Server (NTRS)

    Oman, Luke D.; Douglass, Anne R.

    2014-01-01

    The evolution of ozone is examined in the latest version of the Goddard Earth Observing System Chemistry-Climate Model (GEOSCCM) using old and new ozone-depleting substances (ODS) scenarios. This version of GEOSCCM includes a representation of the quasi-biennial oscillation, a more realistic implementation of ozone chemistry at high solar zenith angles, an improved air/sea roughness parameterization, and an extra 5 parts per trillion of CH3Br to account for brominated very short-lived substances. Together these additions improve the representation of ozone compared to observations. This improved version of GEOSCCM was used to simulate the ozone evolution for the A1 2010 and the newStratosphere-troposphere Processes and their Role in Climate (SPARC) 2013 ODS scenario derived using the SPARC Lifetimes Report 2013. This new ODS scenario results in a maximum Cltot increase of 65 parts per trillion by volume (pptv), decreasing slightly to 60 pptv by 2100. Approximately 72% of the increase is due to the longer lifetime of CFC-11. The quasi-global (60degS-60degN) total column ozone difference is relatively small and less than 1Dobson unit on average and consistent with the 3-4% larger 2050-2080 average Cly in the new SPARC 2013 scenario. Over high latitudes, this small change in Cly compared to the relatively large natural variabilitymakes it not possible to discern a significant impact on ozone in the second half of the 21st century in a single set of simulations.

  6. Coherence of longterm stratospheric ozone time series for the study of ozone recovery in the northern mid-latitudes

    NASA Astrophysics Data System (ADS)

    Nair, Prijitha J.; Godin-Beekmann, Sophie; Pazmino, Andrea

    2010-05-01

    Since mid-to late 1980s decreasing amounts of ozone concentration has been observed in northern mid-latitudes mainly due to the ozone depleting chlorofluorocarbon loading in the stratosphere. Recent works indicate the stabilization of ozone loss in the mid-latitudes, in the upper stratosphere in particular. In order to further investigate the evolution of ozone in the mid-latitudes, a coherent dataset is required. As a first step, we diagnose the long term evolution of ozone at Observatoire de Haute Provence (OHP - 43.93°N, 5.71°E), one of the northern mid-latitude stations. In this study, we present the inter comparison of ozone measurements from OHP LIDAR with collocated SBUV, SAGEII, HALOE, MLS and GOMOS satellite observations as well as the ground based Ozonesondes and Umkehr measurements. A detailed statistical study on the relative differences of the compared measurements is performed to check any specific drifts with time. In addition, the seasonal and annual averages of the relative deviations are also checked to quantify agreement among the data. On average, all instruments show their best agreement with LIDAR between 20 and 40 km, where the differences are within 5%. The agreement with SAGEII measurements are remarkably good since it falls within 1% at 17-41 km. A similar result is also found from the Ozonesondes comparison at 22-31 km. Most comparisons exhibit slightly larger deviations below 20 and above 42 km, of about 10%. The LIDAR masurements are also compared to Umkehr measurements by converting its ozone number density to Dobson units for each Umkehr layer. The analysis reveals a negative bias in Umkehr data within -10% except at layer 6 (around 30 km).

  7. Improvements in total column ozone in GEOSCCM and comparisons with a new ozone-depleting substances scenario

    NASA Astrophysics Data System (ADS)

    Oman, Luke D.; Douglass, Anne R.

    2014-05-01

    The evolution of ozone is examined in the latest version of the Goddard Earth Observing System Chemistry-Climate Model (GEOSCCM) using old and new ozone-depleting substances (ODS) scenarios. This version of GEOSCCM includes a representation of the quasi-biennial oscillation, a more realistic implementation of ozone chemistry at high solar zenith angles, an improved air/sea roughness parameterization, and an extra 5 parts per trillion of CH3Br to account for brominated very short-lived substances. Together these additions improve the representation of ozone compared to observations. This improved version of GEOSCCM was used to simulate the ozone evolution for the A1 2010 and the new Stratosphere-troposphere Processes and their Role in Climate (SPARC) 2013 ODS scenario derived using the SPARC Lifetimes Report 2013. This new ODS scenario results in a maximum Cltot increase of 65 parts per trillion by volume (pptv), decreasing slightly to 60 pptv by 2100. Approximately 72% of the increase is due to the longer lifetime of CFC-11. The quasi-global (60°S-60°N) total column ozone difference is relatively small and less than 1 Dobson unit on average and consistent with the 3-4% larger 2050-2080 average Cly in the new SPARC 2013 scenario. Over high latitudes, this small change in Cly compared to the relatively large natural variability makes it not possible to discern a significant impact on ozone in the second half of the 21st century in a single set of simulations.

  8. Unprecedented 1993 ozone decrease over the United States from Dobson spectrophotometer observations

    SciTech Connect

    Komhyr, W.D.; Grass, R.D.; Evans, R.D.; Leonard, R.K.; Quincy, D.M. ); Hoffman, D.J.; Koenig, G.L. )

    1994-02-01

    Dobson spectrophotometer observations conducted since the early-to-mid 1960's at Bismarck, North Dakota; Caribou, Maine; Boulder, Colorado; Wallops Island, Virginia; Nashville, Tennessee; and at Fresno, California, since 1983, have revealed record low total ozone values during 1993. The tendency toward the low ozone values began in May 1992, but accelerated in early 1993. During January-August 1993, ozone monthly means at the stations were more than 2 standard deviations below long-term normal monthly means 72% of the time and more than 3 standard deviations below normals 42% of the time. On average, the January-April 1993 ozone values were 12.6% below normal, with ozone deficits as large as 18% observed at Caribou and Wallops Island in January. Of particular concern are unusually low ozone values that occur in summertime when solar ultraviolet insolation is high. Such record lows occurred at four of the six stations (Caribou, Wallops Island, Fresno, and Nashville). During May-August 1993, ozone was on average 8.5% below normal at these sites. Monthly means at these stations were, furthermore, lower on average by 3.7% than corresponding lowest values observed there in the past. The ozone decrease of 12.6% below normal at the six continental Dobson instrument stations during the winter and spring months of 1993 implies a possible average increase in UV erythemal radiation at that time of 16-25% above normal. The 8.5% decrease in ozone at Caribou, Wallops Island, Fresno, and Nashville, implies that on average, UV erythemal radiation may have been higher than normal at these stations during the summer of 1993 by 11-17%. 5 refs., 3 figs., 1 tab.

  9. Ozone transport commission developments

    SciTech Connect

    Joyce, K.M.

    1995-08-01

    On September 27, 1994, the states of the Ozone Transport Commission (OTC) signed an important memorandum of understanding (MOU) agreeing to develop a regional strategy for controlling stationary sources of nitrogen oxide emissions. Specifically, the states of the Ozone Transport Region, OTR, agreed to propose regulations for the control of NOx emissions from boilers and other indirect heat exchangers with a maximum gross heat input rate of at least 250 million BTU per hour. The Ozone Transport Region was divided into Inner, Outer and Northern Zones. States in the Outer Zone agreed to reduce NOx emissions by 55%. States in the Inner Zone agreed to reduce NOx emissions 65%. Facilities in both zones have the option to emit NOx at a rate no greater than 0.2 pounds per million Btu by May 1, 1999. This option provides fairness for the gas-fired plants which already have relatively low NOx emissions. Additionally, States in the Inner and Outer Zones agreed to reduce their NOx emissions by 75% or to emit NOx at a rate no greater than 0.15 pounds per million BTU by May 1, 2003. The Northern Zone States agree to reduce their rate of NOx emissions by 55% from base year levels by May 1, 2003, or to emit NOx at a rate no greater than 0.2 pounds per million BTU. As part of this MOU, States also agreed to develop a regionwide trading mechanism to provide a cost-effective mechanism for implementing the reductions.

  10. Ozone measurement systems improvements studies

    NASA Technical Reports Server (NTRS)

    Thomas, R. W.; Guard, K.; Holland, A. C.; Spurling, J. F.

    1974-01-01

    Results are summarized of an initial study of techniques for measuring atmospheric ozone, carried out as the first phase of a program to improve ozone measurement techniques. The study concentrated on two measurement systems, the electro chemical cell (ECC) ozonesonde and the Dobson ozone spectrophotometer, and consisted of two tasks. The first task consisted of error modeling and system error analysis of the two measurement systems. Under the second task a Monte-Carlo model of the Dobson ozone measurement technique was developed and programmed for computer operation.

  11. Assessing the effects of ambient ozone in China on snap bean genotypes by using ethylenediurea (EDU).

    PubMed

    Yuan, Xiangyang; Calatayud, Vicent; Jiang, Lijun; Manning, William J; Hayes, Felicity; Tian, Yuan; Feng, Zhaozhong

    2015-10-01

    Four genotypes of snap bean (Phaseolus vulgaris L.) were selected to study the effects of ambient ozone concentration at a cropland area around Beijing by using 450 ppm of ethylenediurea (EDU) as a chemical protectant. During the growing season, the 8h (9:00-17:00) average ozone concentration was very high, approximately 71.3 ppb, and AOT40 was 29.0 ppm.h. All genotypes showed foliar injury, but ozone-sensitive genotypes exhibited much more injury than ozone-tolerant ones. Compared with control, EDU significantly alleviated foliar injury, increased photosynthesis rate and chlorophyll a fluorescence, Vcmax and Jmax, and seed and pod weights in ozone-sensitive genotypes but not in ozone-tolerant genotypes. EDU did not significantly affect antioxidant contents in any of the genotypes. Therefore, EDU effectively protected sensitive genotypes from ambient ozone damage, while protection on ozone-tolerant genotypes was limited. EDU can be regarded as a useful tool in risk assessment of ambient ozone on food security.

  12. Spatial distribution of tropospheric ozone in national parks of California: interpretation of passive-sampler data.

    PubMed

    Ray, J D

    2001-09-28

    The National Park Service (NPS) has tested and used passive ozone samplers for several years to get baseline values for parks and to determine the spatial variability within parks. Experience has shown that the Ogawa passive samplers can provide +/-10% accuracy when used with a quality assurance program consisting of blanks, duplicates, collocated instrumentation, and a standard operating procedure that carefully guides site operators. Although the passive device does not meet EPA criteria as a certified method (mainly, that hourly values be measured), it does provide seasonal summed values of ozone. The seasonal ozone concentrations from the passive devices can be compared to other monitoring to determine baseline values, trends, and spatial variations. This point is illustrated with some kriged interpolation maps of ozone statistics. Passive ozone samplers were used to get elevational gradients and spatial distributions of ozone within a park. This was done in varying degrees at Mount Rainier, Olympic, Sequoia-Kings Canyon, Yosemite, Joshua Tree, Rocky Mountain, and Great Smoky Mountains national parks. The ozone has been found to vary by factors of 2 and 3 within a park when average ozone is compared between locations. Specific examples of the spatial distributions of ozone in three parks within California are given using interpolation maps. Positive aspects and limitations of the passive sampling approach are presented.

  13. Influence of isentropic transport on seasonal ozone variations in the lower stratosphere and subtropical upper troposphere

    NASA Technical Reports Server (NTRS)

    Jing, P.; Cunnold, D. M.; Yang, E.-S.; Wang, H.-J.

    2005-01-01

    The isentropic cross-tropopause ozone transport has been estimated in both hemispheres in 1999 based on the potential vorticity mapping of Stratospheric Aerosol and Gas Experiment 11 ozone measurements and contour advection calculations using the NASA Goddard Space Flight Center Global and Modeling Assimilation Office analysis. The estimated net isentropic stratosphere-to-troposphere ozone flux is approx.118 +/- 61 x 10(exp9)kg/yr globally within the layer between 330 and 370 K in 1999; 60% of it is found in the Northern Hemisphere, and 40% is found in the Southern Hemisphere. The monthly average ozone fluxes are strongest in summer and weakest in winter in both hemispheres. The seasonal variations of ozone in the lower stratosphere (LS) and upper troposphere (UT) have been analyzed using ozonesonde observations from ozonesonde stations in the extratropics and subtropics, respectively. It is shown that observed ozone levels increase in the UT over subtropical ozonesonde stations and decrease in the LS over extratropical stations in late spring/early summer and that the ozone increases in the summertime subtropical UT are unlikely to be explained by photochemical ozone production and diabatic transport alone. We conclude that isentropic transport is a significant contributor to ozone levels in the subtropical upper troposphere, especially in summer.

  14. Magnitude, decadal changes, and impact of regional background ozone transported into the greater Houston, Texas, area.

    PubMed

    Berlin, Shaena R; Langford, Andrew O; Estes, Mark; Dong, Melody; Parrish, David D

    2013-12-17

    Two independent analyses of the daily maximum 8 h average ozone concentrations measured during the high ozone season (May through October) at Continuous Ambient Monitoring Stations are used to quantify the regional background ozone transported into the Houston-Galveston-Brazoria (HGB) area. The dependence on wind direction is examined, and long-term trends are determined using measurements made between 1998 and 2012. Both analyses show that the regional background ozone has declined during periods of continental outflow: i.e., the conditions associated with most high ozone episodes in HGB. The changes in regional background ozone found for northeasterly and southeasterly flow are -0.50 ± 0.54 and -0.79 ± 0.65 (95% confidence limit) ppbv yr(-1), respectively, which correspond to decreases of ∼7-11 ppbv between 1998 and 2012. This finding is consistent with the summertime downward trend of -0.45 ppbv yr(-1) (range of sites: -0.87 to +0.07 ppbv yr(-1)) for ozone in the eastern U.S. between 1990 and 2010 reported by Cooper et al. and shows that changing background concentrations are at least partially responsible for the decreased surface ozone in the HGB area over the past decade. Baseline ozone concentrations in air flowing into Texas from the Gulf of Mexico have not changed significantly over this period.

  15. Simulations of ozone distributions in an aircraft cabin using computational fluid dynamics

    NASA Astrophysics Data System (ADS)

    Rai, Aakash C.; Chen, Qingyan

    2012-07-01

    Ozone is a major pollutant of indoor air. Many studies have demonstrated the adverse health effect of ozone and the byproducts generated as a result of ozone-initiated reactive chemistry in an indoor environment. This study developed a Computational Fluid Dynamics (CFD) model to predict the ozone distribution in an aircraft cabin. The model was used to simulate the distribution of ozone in an aircraft cabin mockup for the following cases: (1) empty cabin; (2) cabin with seats; (3) cabin with soiled T-shirts; (4) occupied cabin with simple human geometry; and (5) occupied cabin with detailed human geometry. The agreement was generally good between the CFD results and the available experimental data. The ozone removal rate, deposition velocity, retention ratio, and breathing zone levels were well predicted in those cases. The CFD model predicted breathing zone ozone concentration to be 77-99% of the average cabin ozone concentration depending on the seat location. The ozone concentration at the breathing zone in the cabin environment can better assess the health risk to passengers and can be used to develop strategies for a healthier cabin environment.

  16. Long-term tropical tropospheric ozone column retrievals using the Convective Clouds Differential (CCD) technique

    NASA Astrophysics Data System (ADS)

    Leventidou, Elpida; Ebojie, Felix; Eichmann, Kai-Uwe; Weber, Mark; Burrows, John P.

    2015-04-01

    Ozone influences most of the chemical reactions in the troposphere.Its tropospheric abundance can be retrieved using space-borne observations of vertically integrated ozone and cloud heights. The Convective Clouds Differential (CCD) technique (Ziemke et al., 1998 and Valks et al., 2014) takes advantage of the frequent occurrence of convective clouds in the western Pacific region by subtracting above-cloud ozone of this region from clear-sky ozone elsewhere to derive global monthly mean tropospheric amount. An important assumption is that the above-cloud ozone in the western Pacific simulates the stratospheric ozone and that the stratospheric ozone field is invariant with longitude; which is approximately true in the tropics. A CCD algorithm has been developed and is applied to optical remote sensing observations from three satellite instruments, so that a unique long-term record of monthly averaged tropical (20∘S, 20∘N) tropospheric vertically integrated ozone (1995-2012) is created. The validation of the CCD results with tropospheric ozone data from ozonesondes (Tompson et al., 2003) and Limb-Nadir matching observations (Ebojie et al. 2014) will be presented.

  17. Averaging Models: Parameters Estimation with the R-Average Procedure

    ERIC Educational Resources Information Center

    Vidotto, G.; Massidda, D.; Noventa, S.

    2010-01-01

    The Functional Measurement approach, proposed within the theoretical framework of Information Integration Theory (Anderson, 1981, 1982), can be a useful multi-attribute analysis tool. Compared to the majority of statistical models, the averaging model can account for interaction effects without adding complexity. The R-Average method (Vidotto &…

  18. Photochemical roles of rapid economic growth and potential abatement strategies on tropospheric ozone over South and East Asia in 2030

    NASA Astrophysics Data System (ADS)

    Chatani, S.; Amann, M.; Goel, A.; Hao, J.; Klimont, Z.; Kumar, A.; Mishra, A.; Sharma, S.; Wang, S. X.; Wang, Y. X.; Zhao, B.

    2014-04-01

    A regional air quality simulation framework including the Weather Research and Forecasting modelling system (WRF), the Community Multi-scale Air Quality modeling system (CMAQ), and precursor emissions to simulate tropospheric ozone over South and East Asia is introduced. Concentrations of tropospheric ozone and related species simulated by the framework are validated by comparing with observation data of surface monitorings, ozone zondes, and satellites obtained in 2010. The simulation demonstrates acceptable performance on tropospheric ozone over South and East Asia at regional scale. Future energy consumption, carbon dioxide (CO2), nitrogen oxides (NOx), and volatile organic compound (VOC) emissions in 2030 under three future scenarios are estimated. One of the scenarios assumes a business-as-usual (BAU) pathway, and other two scenarios consider implementation of additional energy and environmental strategies to reduce energy consumption, CO2, NOx, and VOC emissions in China and India. Future surface ozone under these three scenarios is predicted by the simulation. The simulation indicates future surface ozone significantly increases around India for a whole year and around north eastern China in summer. NOx is a main driver on significant seasonal increase of surface ozone, whereas VOC as well as increasing background ozone and methane is also an important factor on annual average of surface ozone in East Asia. Warmer weather around India is also preferable for significant increase of surface ozone. Additional energy and environmental strategies assumed in future scenarios are expected to be effective to reduce future surface ozone over South and East Asia.

  19. SWIFT: Semi-empirical and numerically efficient stratospheric ozone chemistry for global climate models

    NASA Astrophysics Data System (ADS)

    Kreyling, Daniel; Wohltmann, Ingo; Lehmann, Ralph; Rex, Markus

    2015-04-01

    The SWIFT model is a fast yet accurate chemistry scheme for calculating the chemistry of stratospheric ozone. It is mainly intended for use in Global Climate Models (GCMs), Chemistry Climate Models (CCMs) and Earth System Models (ESMs). For computing time reasons these models often do not employ full stratospheric chemistry modules, but use prescribed ozone instead. This can lead to insufficient representation between stratosphere and troposphere. The SWIFT stratospheric ozone chemistry model, focuses on the major reaction mechanisms of ozone production and loss in order to reduce the computational costs. SWIFT consists of two sub-models. 1) Inside the polar vortex, the model calculates polar vortex averaged ozone loss by solving a set of coupled differential equations for the key species in polar ozone chemistry. 2) The extra-polar regime, which this poster is going to focus on. Outside the polar vortex, the complex system of differential equations of a full stratospheric chemistry model is replaced by an explicit algebraic polynomial, which can be solved in a fraction of the time needed by the full scale model. The approach, which is used to construct the polynomial, is also referred to as repro-modeling and has been successfully applied to chemical models (Turanyi (1993), Lowe & Tomlin (2000)). The procedure uses data from the Lagrangian stratospheric chemistry and transport model ATLAS and yields one high-order polynomial for global ozone loss and production rates over 24h per month. The stratospheric ozone change rates can be sufficiently described by 9 variables. Latitude, altitude, temperature, the overhead ozone abundance, 4 mixing ratios of ozone depleting chemical families (chlorine, bromine, nitrogen-oxides and hydrogen-oxides) and the ozone concentrations itself. The ozone change rates in the lower stratosphere as a function of these 9 variables yield a sufficiently compact 9-D hyper-surface, which we can approximate with a polynomial. In the upper

  20. Evaluating 2012 Ozone Impacts of Natural Gas Development in the Haynesville Shale with an Updated Emission Inventory

    NASA Astrophysics Data System (ADS)

    Kemball-Cook, S. R.; Bar-Ilan, A.; Yarwood, G.

    2013-12-01

    The Haynesville Shale, located approximately 10,000-13,000 feet beneath Northeast Texas and Northwest Louisiana contains very large recoverable reserves of natural gas. Development of the Haynesville began in 2008, and since then, more than 3,000 wells have been drilled. The development of natural gas resources in the Haynesville is economically important, but also generates emissions of ozone precursors in a region with several ozone monitors that are close to or exceeding the 2008 National Ambient Air Quality Standard. During 2009, we developed an emission inventory of ozone precursors for projected future Haynesville Shale development from 2009 through 2020. Photochemical modeling with the 2012 emission inventory showed significant ozone impacts within Northeast Texas and Northwest Louisiana as a result of Haynesville emissions, with projected 8-hour ozone design value increases up to 5 ppb at area monitors. The original emission inventory was assembled during spring 2009, early in the development of the Haynesville when available data were limited. Since then, development in the Haynesville has continued, and additional data are now available and were used to refine the development projections and emission inventory through the year 2020. The updated 2012 emission inventory is now based on actual data rather than projections made in 2009. The number of drilling rigs operating in 2012 was lower than projected, but the well count was higher due intensive drilling activity in 2010-2011 that exceeded projections. The updated emission inventory draws on more Haynesville-specific data than the previous inventory. Energy producers currently active in the Haynesville were surveyed and provided information that included well drilling times, equipment used for well construction, production equipment present at typical Haynesville wells, and produced gas composition analyses. Producers provided information on the amount of truck traffic associated with transport of

  1. Role of tropospheric ozone increases in 20th-century climate change

    NASA Astrophysics Data System (ADS)

    Shindell, Drew; Faluvegi, Greg; Lacis, Andrew; Hansen, James; Ruedy, Reto; Aguilar, Elliot

    2006-04-01

    Human activities have increased tropospheric ozone, contributing to 20th-century warming. Using the spatial and temporal distribution of precursor emissions, we simulated tropospheric ozone from 1890 to 1990 using the NASA Goddard Institute for Space Studies (GISS) chemistry model. Archived three-dimensional ozone fields were then used in transient GISS climate model simulations. This enables more realistic evaluation of the impact of tropospheric ozone increases than prior simulations using an interpolation between preindustrial and present-day ozone. We find that tropospheric ozone contributed to the greater 20th-century warming in the Northern Hemisphere extratropics compared with the tropics and in the tropics compared with the Southern Hemisphere extratropics. Additionally, ozone increased more rapidly during the latter half of the century than the former, causing more rapid warming during that time. This is especially apparent in the tropics and is consistent with observations, which do not show similar behavior in the extratropics. Other climate forcings do not substantially accelerate warming rates in the tropics relative to other regions. This suggests that accelerated tropospheric ozone increases related to industrialization in the developing world have contributed to the accelerated tropical warming. During boreal summer, tropospheric ozone causes enhanced warming (>0.5°C) over polluted northern continental regions. Finally, the Arctic climate response to tropospheric ozone increases is large during fall, winter, and spring when ozone's lifetime is comparatively long and pollution transported from midlatitudes is abundant. The model indicates that tropospheric ozone could have contributed about 0.3°C annual average and about 0.4°C-0.5°C during winter and spring to the 20th-century Arctic warming. Pollution controls could thus substantially reduce the rapid rate of Arctic warming.

  2. Size-mediated foliar response to ozone in black cherry trees.

    PubMed

    Fredericksen, T S; Skelly, J M; Steiner, K C; Kolb, T E; Kouterick, K B

    1996-01-01

    Local ozone concentration and visible foliar injury were measured over the 1994 growing season on open-grown black cherry (Prunus serotina Ehrh.) trees of varying size (age) within forest stands and adjacent openings at a site in north-central Pennsylvania. Relationships were determined between visible ozone injury and ozone exposure, as well as calculated between injury and ozone uptake expressed as the product of stomatal conductance and ozone concentration. In addition, simultaneous measurements of visible symptoms and leaf gas exchange were also conducted to determine the correlation between visible and physiological injury and ozone exposure. By September, the amount of leaf area affected by visible foliar ozone injury was greatest for seedlings (46%), followed by canopy trees (20%) and saplings (15%). A large amount of variability in foliar ozone symptom expression was observed among trees within a size class. Sum40 and Sum60 (ozone concentration > 40 and > 60 nl liter(-1)) cumulative exposure statistics were the most meaningful indices for interpretation of foliar injury response. Seedlings were apparently more sensitive to ozone injury than larger trees because their higher rates of stomatal conductance resulted in higher rates of ozone uptake. Seedlings also had higher rates of early leaf abscission than larger trees with an average of nearly 30% of the leaves on a shoot abscised by 1 September compared to approximately 5% for larger trees. However, per unit ozone uptake into the leaf, larger trees exhibited larger amounts of foliar injury. The amount of visible foliar injury was negatively correlated (r(2) = 0.82) with net photosynthetic rates, but was not related to stomatal conductance. Net photosynthesis and stomatal conductance thus became uncoupled at high levels of visible foliar injury. PMID:15091453

  3. Comparison of satellite measurements of ozone and ozone trends

    SciTech Connect

    Rusch, D.W.; Clancy, R.T.; Bhartia, P.K. |

    1994-10-01

    Measurements of ozone retrieved from satellite instruments over the 1979-1991 period are compared. The instruments used are the total ozone mapping spectrometer (TOMS), the solar backscattered ultraviolet experiment (SBUV), and stratospheric aerosol and gas experiments (SAGE) I and II. Although there is good agreement between the absolute densities of ozone as measured by the various instruments, the long-term changes (1979-1990) disagree sharply as a function of pressure and in the integrated ozone amount. In the upper stratosphere, SBUV trends are negative with maximum values of about -1.5%/year at high latitudes. Combined SAGE I and II trends are slightly positive in this region and peak near 0.5%/year at equatorial latitudes. In the lower stratosphere, SBUV trends reflect small decreases in ozone, generally less than -0.4%/year except at high southern latitudes where the trends rearch values of approximately -1.5%/year. SAGE ozone trends exhibit large decreases particularly in the equatorial regions where decreases of 3-6%/year are seen at pressures between 60 and 90 mbar. At higher latitudes, SAGE trends are more comparable to SBUV trends in the lower stratosphere. Total ozone trends from TOMS and SBUV agree within their uncertainties. Near-zero trends are indicated at low latitudes, and larger, negative trends (approximately -0.5%/year) are indicated near the poles. The SAGE column ozone trends depend upon the base level altitude of integration but do not exhibit a strong latitude dependence.

  4. Ultraviolet Radiation and Stratospheric Ozone

    NASA Technical Reports Server (NTRS)

    Stolarski, R.

    2003-01-01

    Ultraviolet radiation from the sun produces ozone in the stratosphere and it participates in the destruction of ozone. Absorption of solar ultraviolet radiation by ozone is the primary heating mechanism leading to the maximum in temperature at the stratopause. Variations of solar ultraviolet radiation on both the 27-day solar rotation period and the 11-year solar cycle affect ozone by several mechanisms. The temperature and ozone in the upper stratosphere respond to solar uv variations as a coupled system. An increase in uv leads to an increase in the production of ozone through the photolysis of molecular oxygen. An increase in uv leads to an increase in temperature through the heating by ozone photolysis. The increase in temperature leads to a partially-offsetting decrease in ozone through temperature-dependent reaction rate coefficients. The ozone variation modulates the heating by ozone photolysis. The increase in ozone at solar maximum enhances the uv heating. The processes are understood and supported by long-term data sets. Variation in the upper stratospheric temperatures will lead to a change in the behavior of waves propagating upward from the troposphere. Changes in the pattern of wave dissipation will lead to acceleration or deceleration of the mean flow and changes in the residual or transport circulation. This mechanism could lead to the propagation of the solar cycle uv variation from the upper stratosphere downward to the lower stratosphere. This process is not well-understood and has been the subject of an increasing number of model studies. I will review the data analyses for solar cycle and their comparison to model results.

  5. Averaging Internal Consistency Reliability Coefficients

    ERIC Educational Resources Information Center

    Feldt, Leonard S.; Charter, Richard A.

    2006-01-01

    Seven approaches to averaging reliability coefficients are presented. Each approach starts with a unique definition of the concept of "average," and no approach is more correct than the others. Six of the approaches are applicable to internal consistency coefficients. The seventh approach is specific to alternate-forms coefficients. Although the…

  6. The Average of Rates and the Average Rate.

    ERIC Educational Resources Information Center

    Lindstrom, Peter

    1988-01-01

    Defines arithmetic, harmonic, and weighted harmonic means, and discusses their properties. Describes the application of these properties in problems involving fuel economy estimates and average rates of motion. Gives example problems and solutions. (CW)

  7. Plant responses to tropospheric ozone

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Tropospheric ozone is the second most abundant air pollutant and an important component of the global climate change. Over five decades of research on the phytotoxicity of ozone in model plants systems, crop plants and forest trees have provided some insight into the physiological, biochemical and m...

  8. Nonaqueous ozonation of vulcanized rubber

    SciTech Connect

    Serkiz, S.M.

    1999-12-07

    A process and resulting product are provided in which a solid particulate, such as vulcanized crumb rubber, has the surface functional groups oxidized by ozonation using a nonpolar solvent. The ozonation process renders the treated crumb rubber more suitable for use in new rubber formulations. As a result, larger loading levels of the treated crumb rubber can be used in new rubber mixtures.

  9. Rocket ozone sounding network data

    NASA Technical Reports Server (NTRS)

    Wright, D. U.; Krueger, A. J.; Foster, G. M.

    1979-01-01

    During the period March 1977 through May 1977, three regular monthly ozone profiles were measured at Wallops Flight Center and three regular monthly ozone profiles were measured at the Churchill Research Range. One additional flight was conducted at Wallops Flight Center in support of Nimbus 4 SBUV. Data results and flight profiles for the period covered are presented.

  10. Atmospheric iodine abates smog ozone.

    PubMed

    HAMILTON, W F; LEVINE, M; SIMON, E

    1963-04-12

    Traces of iodine in test samples of irradiated photochemical smog atmospheres either inhibit ozone formation or lower its concentration. Eye and respiratory irritation are reduced qualitatively. Iodine is more effective in suppressing ozone in a photochemical smog atmosphere than it is in purified air.

  11. Modelling the Antarctic ozone hole

    NASA Technical Reports Server (NTRS)

    Crutzen, P. J.; Bruhl, C.

    1988-01-01

    Researchers performed model calculations of the ozone depletions taking place in the Antarctic lower stratosphere. Making the assumption that odd nitrogen is frozen out on stratospheric haze particles, an analysis is given of how much homogeneous reactions can contribute to ozone loss during September-October. Comparisons with observations indicate the potential importance of reactions with HCl in the polar stratospheric cloud particles.

  12. Nonaqueous ozonation of vulcanized rubber

    DOEpatents

    Serkiz, Steven M.

    1999-01-01

    A process and resulting product is provided in which a solid particulate, such as vulcanized crumb rubber, has the surface functional groups oxidized by ozonation using a nonpolar solvent. The ozonation process renders the treated crumb rubber more suitable for use in new rubber formulations. As a result, larger loading levels of the treated crumb rubber can be used in new rubber mixtures.

  13. Rocket ozone sounding network data

    NASA Technical Reports Server (NTRS)

    Wright, D. U.; Krueger, A. J.; Foster, G. M.

    1978-01-01

    During the period December 1976 through February 1977, three regular monthly ozone profiles were measured at Wallops Flight Center, two special soundings were taken at Antigua, West Indies, and at the Churchill Research Range, monthly activities were initiated to establish stratospheric ozone climatology. This report presents the data results and flight profiles for the period covered.

  14. Simplified ozone detection by chemiluminescence

    NASA Technical Reports Server (NTRS)

    Conway, E. J.; Rogowski, R. S.; Richards, R. R.

    1977-01-01

    Ozone is detected by film coated with solid, such as rubrene, that reacts with ozone to degree proportional to concentration in sample gas. Gas flow is stopped, and film is heated to produce light (chemiluminescence) in proportion to amount of reacted material on sensor.

  15. Source attribution of tropospheric ozone

    NASA Astrophysics Data System (ADS)

    Butler, T. M.

    2015-12-01

    Tropospheric ozone is a harmful pollutant with adverse effects on human health and ecosystems. As well as these effects, tropospheric ozone is also a powerful greenhouse gas, with an anthropogenic radiative forcing one quarter of that of CO2. Along with methane and atmospheric aerosol, tropospheric ozone belongs to the so-called Short Lived Climate forcing Pollutants, or SLCP. Recent work has shown that efforts to reduce concentrations of SLCP in the atmosphere have the potential to slow the rate of near-term climate change, while simultaneously improving public health and reducing crop losses. Unlike many other SLCP, tropospehric ozone is not directly emitted, but is instead influenced by two distinct sources: transport of air from the ozone-rich stratosphere; and photochemical production in the troposphere from the emitted precursors NOx (oxides of nitrogen), CO (Carbon Monoxide), and VOC (volatile organic compounds, including methane). Better understanding of the relationship between ozone production and the emissions of its precursors is essential for the development of targeted emission reduction strategies. Several modeling methods have been employed to relate the production of tropospheric ozone to emissions of its precursors; emissions perturbation, tagging, and adjoint sensitivity methods all deliver complementary information about modelled ozone production. Most studies using tagging methods have focused on attribution of tropospheric ozone production to emissions of NOx, even though perturbation methods have suggested that tropospheric ozone is also sensitive to VOC, particularly methane. In this study we describe the implementation into a global chemistry-climate model of a scheme for tagging emissions of NOx and VOC with an arbitrary number of labels, which are followed through the chemical reactions of tropospheric ozone production in order to perform attribution of tropospehric ozone to its emitted precursors. Attribution is performed to both

  16. Direct measurements of tropospheric ozone from TOMS data

    NASA Technical Reports Server (NTRS)

    Hudson, Robert D.

    1993-01-01

    In the past year, we have made measurements of the tropospheric total column of ozone during the biomass burning season in Africa (August to October). Fishman et. al. had reported previously that by taking a time average of the low spatial resolution data from TOMS (Total Ozone Mapping Spectrometer) on Nimbus-7 (referred to as the Grid-T data set), during the biomass burning season in Africa, a plume of ozone extends from the East coast of Africa into the Atlantic. In this report, we present an analysis that we have made using the measured TOMS radiances taken from the High Density TOMS data set (referred as the HDT data set), which examines this plume in more detail.

  17. The neuron network forecasting dynamics of the ozone layer

    NASA Astrophysics Data System (ADS)

    Lankin, J.; Sakash, I.

    One of the major tasks today is preserving the Earth's ozonosphere, - because the ozone layer serves as a screen, filtering a part of harmful solar ultraviolet radiation. During the recent decades, some scientists of different countries have paid their attention to significant decrease of ozone density in the atmosphere above certain points of the Earth's surface. If the average ozone concentration in the atmosphere is about 300-350 D. u., its annual drop above the Antarctic continent follows to the values of concentration even of 90 D. u. Such -- and similar -- publications have triggered widespread public interest (tied to the global environmental crisis); the phenomenon has been named "an ozone hole" and followed by an explosion of scientific interest to ozonospheric studies. In order to simulate hourly TOC oscillations, the ground observation data (City of Tomsk, Russia - 56 N and 84 E) has been used. The following models of ÒÎÑ have been designed: hourly (hourly CCO values are been forecasted for March 30 and 31, 1996-99), diurnal (June 14 -- October 31, 1998), monthly (September 1975 -- August 1977) and annual (1975-1982) ones. The study performed has proven a high degree of effectiveness of using neuron networks for simulating the dynamics of the Earth's ozonosphere. A real opportunity to design local prognostic models using neuronets is revealed. In future, some three-dimentional global models of ozonosphere and atmosphere may be established. However, there a number of cases of significant variations of the ozone concentration time rows for different seasons and time spans. Studying and predicting such changes is of the great interest in terms of better understanding the specifics of developing the atmospheric processes and improving the technology of the forecast. The study is focused upon revealing the precursors of the spontaneous "ozone hole" (areas of the lowered concentration of ozone) formation in the stratosphere and based on neuron network

  18. Ozone adsorption on carbon nanoparticles

    NASA Astrophysics Data System (ADS)

    Chassard, Guillaume; Gosselin, Sylvie; Visez, Nicolas; Petitprez, Denis

    2014-05-01

    Carbonaceous particles produced by incomplete combustion or thermal decomposition of hydrocarbons are ubiquitous in the atmosphere. On these particles are adsorbed hundreds of chemical species. Those of great concern to health are polycyclic aromatic hydrocarbons (PAHs). During atmospheric transport, particulate PAHs react with gaseous oxidants. The induced chemical transformations may change toxicity and hygroscopicity of these potentially inhalable particles. The interaction between ozone and carbon particles has been extensively investigated in literature. However ozone adsorption and surface reaction mechanisms are still ambiguous. Some studies described a fast catalytic decomposition of ozone initiated by an atomic oxygen chemisorption followed by a molecular oxygen release [1-3]. Others suggested a reversible ozone adsorption according to Langmuir-type behaviour [4,5]. The aim of this present study is a better understanding of ozone interaction with carbon surfaces. An aerosol of carbon nanoparticles was generated by flowing synthetic air in a glass tube containing pure carbon (primary particles < 50 nm), under magnetic stirring. The aerosol was then mixed with ozone in an aerosol flow tube. Ozone uptake experiments were performed with different particles concentrations with a fixed ozone concentration. The influence of several factors on kinetics was examined: initial ozone concentration, particle size (50 nm ≤ Dp ≤ 200 nm) and competitive adsorption (with probe molecule and water). The effect of initial ozone concentration was first studied. Accordingly to literature, it has been observed that the number of gas-phase ozone molecules lost per unit particle surface area tends towards a plateau for high ozone concentration suggesting a reversible ozone adsorption according to a Langmuir mechanism. We calculated the initial reaction probability between O3 and carbon particles.An initial uptake coefficient of 1.10-4 was obtained. Similar experiments were

  19. Latest tendency in the Antarctic ozone longitudinal distribution

    NASA Astrophysics Data System (ADS)

    Milinevsky, Gennadi; Grytsai, Asen; Klekociuk, Andrew; Evtushevsky, Olexander

    2014-05-01

    Significant ozone depletion was observed within the southern polar vortex during spring in the 1980s - early 1990s. Later, a stabilization in total ozone levels and ozone hole area has been observed. Atmosphere models predict a consequent recovery of the Antarctic ozone. Nevertheless, identification of the long-term processes is complicated by high interannual variability hiding their general regularities. In particular, a large stratosphere warming in 2002 resulted in significant increase in total ozone levels. The Antarctic ozone hole is formed inside polar stratospheric vortex, which is under influence of large-scale planetary waves. The components of the quasi-stationary wave (QSW) in the spring Southern Hemisphere (SH) stratosphere is mainly contributed by zonal wave number 1 which in turn determines the location of the total ozone extremes in spring: QSW minimum (maximum) is located in the South Atlantic (Australian) sector. In our work the satellite data of TOMS/Nimbus-7, TOMS/Earth Probe and OMI/Aura (http://ozoneaq.gsfc.nasa.gov/) have been used to investigate longitudinal distribution of the total ozone in Antarctic region. The gap in these satellite observations (1993-1995) was filled by the Multi-Sensor Reanalysis data (http://www.temis.nl/). Ozone distribution in the SH high and mid latitudes 80-50S were analyzed for southern spring season including months from September to November. The zonal distribution is considered along seven latitude circles from 80S to 50S with step of five degrees. To distinguish long-term processes and to obtain a quasi-stationary pattern, daily September - November ozone was averaged. Our previous study demonstrated a systematic eastward shift of the QSW minimum region. In this study, we extended the analysis to 2013 and obtained new results that exhibited a probable cessation in that eastward shift. Polynomial fit for all chosen latitudes is even evidence of a change in the tendency to opposite. It more time needs to

  20. Trends of Rural Tropospheric Ozone at the Northwest of the Iberian Peninsula

    PubMed Central

    Saavedra, S.; Rodríguez, A.; Souto, J. A.; Casares, J. J.; Bermúdez, J. L.; Soto, B.

    2012-01-01

    Tropospheric ozone levels around urban and suburban areas at Europe and North America had increased during 80's–90's, until the application of NOx reduction strategies. However, as it was expected, this ozone depletion was not proportional to the emissions reduction. On the other hand, rural ozone levels show different trends, with peaks reduction and average increments; this different evolution could be explained by either emission changes or climate variability in a region. In this work, trends of tropospheric ozone episodes at rural sites in the northwest of the Iberian Peninsula were analyzed and compared to others observed in different regions of the Atlantic European coast. Special interest was focused on the air quality sites characterization, in order to guarantee their rural character in terms of air quality. Both episodic local meteorological and air quality measurements along five years were considered, in order to study possible meteorological influences in ozone levels, different to other European Atlantic regions. PMID:22649298