Questions and answers about the effects of the depletion of the ozone layer on humans and the environment.

PubMed

Aucamp, Pieter J

2007-03-01

The ozone molecule contains three atoms of oxygen and is mainly formed by the action of the ultraviolet rays of the sun on the diatomic oxygen molecules in the upper part of the Earth's atmosphere (called the stratosphere). Atmospheric pollution near the Earth's surface can form localized areas of ozone. The stratospheric ozone layer protects life on Earth by absorbing most of the harmful ultraviolet radiation from the sun. In the mid 1970s it was discovered that some manmade products destroy ozone molecules in the stratosphere. This destruction can result in damage to ecosystems and to materials such as plastics. It may cause an increase in human diseases such as skin cancers and cataracts. The discovery of the role of the synthetic ozone-depleting chemicals such as chlorofluorocarbons (CFCs) stimulated increased research and monitoring in this field. Computer models predicted a disaster if no action was taken to protect the ozone layer. Based on this research and monitoring, the nations of the world took action in 1985 with the Vienna Convention for the Protection of the Ozone Layer followed by the Montreal Protocol on Substances that Deplete the Ozone Layer in 1987. The Convention and Protocol were amended and adjusted several times as new knowledge was obtained. The Meetings of the Parties to the Montreal Protocol appointed three Assessment Panels to review the progress in scientific knowledge on their behalf. These panels are the Scientific Assessment Panel, the Technological and Economic Assessment Panel and the Environmental Effects Assessment Panel. Each panel covers a designated area and there is a natural level of overlap. The main reports of the Panels are published every four years as required by the Meeting of the Parties. All the reports have an executive summary that is distributed more widely than the main report itself. It became customary to add a set of questions and answers--mainly for non-expert readers--to the executive summaries. This document contains the questions and answers prepared by experts who comprise the Environmental Assessment Panel. It is based mainly on the 2006 report of the Panel but also contains information from previous assessments. Readers who need detailed information on any question should consult the full reports for a more complete scientific discussion. This set of questions refers mainly to the environmental effects of ozone depletion and climate change. The report of the Scientific Assessment Panel contains questions and answers related to the other scientific issues addressed by that Panel. All these reports can be found on the UNEP website (http://ozone.unep.org).

Scientific assessment of stratospheric ozone: 1989, volume 1

NASA Technical Reports Server (NTRS)

1990-01-01

A scientific review is presented of the current understanding of stratospheric ozone. There have been highly significant advances in the understanding of the impact of human activities on the Earth's protective ozone layer. There are four major findings that each heighten the concern that chlorine and bromine containing chemicals can lead to a significant depletion of stratospheric ozone: (1) Antarctic ozone hole (the weight of evidence indicates that chlorinated and brominated chemicals are responsible for the ozone hole; (2) Perturbed arctic chemistry (the same potentially ozone destroying processes were identified in the Arctic stratosphere); (3) Long term ozone decreases; and (4) Model limitations (gaps in theoretical models used for assessment studies).

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…

Ozone depletion and solar ultraviolet radiation: ocular effects, a United nations environment programme perspective.

PubMed

Cullen, Anthony P

2011-07-01

To describe he role played by the United Nations Environmental Effects Panel with respect to the ocular effects of stratospheric ozone depletion and present the essence of the Health Chapter of the 2010 Assessment. A consideration of solar ultraviolet radiation (UVR) at the Earth's surface as it is affected by atmospheric changes and how these influence sunlight-related eye diseases. A review of the current Assessment with emphasis on pterygium, cataract, ocular melanoma, and age-related macular degeneration. Although the ozone layer is projected to recover slowly in the coming decades, continuing vigilance is required regarding exposure to the sun. Evidence implicating solar UVR, especially UVB, in every tissue of the eye continues to be amassed. The need for ocular UV protection existed before the discovery of the depletion of the ozone layer and will continue even when the layer fully recovers in approximately 2100.

Evidence for a Continuous Decline in Lower Stratospheric Ozone Offsetting Ozone Layer Recovery

NASA Technical Reports Server (NTRS)

Ball, William T.; Alsing, Justin; Mortlock, Daniel J.; Staehelin, Johannes; Haigh, Joanna D.; Peter, Thomas; Tummon, Fiona; Stuebi, Rene; Stenke, Andrea; Anderson, John;

Evidence for a continuous decline in lower stratospheric ozone offsetting ozone layer recovery

NASA Astrophysics Data System (ADS)

Ball, William T.; Alsing, Justin; Mortlock, Daniel J.; Staehelin, Johannes; Haigh, Joanna D.; Peter, Thomas; Tummon, Fiona; Stübi, Rene; Stenke, Andrea; Anderson, John; Bourassa, Adam; Davis, Sean M.; Degenstein, Doug; Frith, Stacey; Froidevaux, Lucien; Roth, Chris; Sofieva, Viktoria; Wang, Ray; Wild, Jeannette; Yu, Pengfei; Ziemke, Jerald R.; Rozanov, Eugene V.

2018-02-01

Ozone forms in the Earth's atmosphere from the photodissociation of molecular oxygen, primarily in the tropical stratosphere. It is then transported to the extratropics by the Brewer-Dobson circulation (BDC), forming a protective ozone layer around the globe. Human emissions of halogen-containing ozone-depleting substances (hODSs) led to a decline in stratospheric ozone until they were banned by the Montreal Protocol, and since 1998 ozone in the upper stratosphere is rising again, likely the recovery from halogen-induced losses. Total column measurements of ozone between the Earth's surface and the top of the atmosphere indicate that the ozone layer has stopped declining across the globe, but no clear increase has been observed at latitudes between 60° S and 60° N outside the polar regions (60-90°). Here we report evidence from multiple satellite measurements that ozone in the lower stratosphere between 60° S and 60° N has indeed continued to decline since 1998. We find that, even though upper stratospheric ozone is recovering, the continuing downward trend in the lower stratosphere prevails, resulting in a downward trend in stratospheric column ozone between 60° S and 60° N. We find that total column ozone between 60° S and 60° N appears not to have decreased only because of increases in tropospheric column ozone that compensate for the stratospheric decreases. The reasons for the continued reduction of lower stratospheric ozone are not clear; models do not reproduce these trends, and thus the causes now urgently need to be established.

The Military's Role in Protection of the Ozone Layer.

ERIC Educational Resources Information Center

Anderson, Stephen O.; And Others

1994-01-01

This articles examines the possibility that military organizations may find that common environmental problems serve as a basis for establishing new relationships outside traditional alliances that otherwise would not be possible. The elimination of the need for chloroflourocarbons, halons, and other ozone-depleting substances is used as an…

The president speaks: prevention is best: lessons from protecting the ozone layer.

PubMed

Woodcock, Ashley

2012-12-01

The Montreal Protocol was signed 25 years ago. As a result, the irreversible destruction of the ozone layer was prevented. However, stratospheric ozone will not recover completely until 2060 and the consequent epidemic in skin cancer cases will persist until 2100. Many millions of patients with asthma and chronic obstructive pulmonary disease have safely switched from chlorofluorocarbon (CFC)-powered metered-dose inhalers (MDIs) to either hydrofluorocarbon (HFC) or DPIs. China will be the last country to phase out CFCs by 2016. HFCs are global warming gases which will be controlled in the near future. HFCs in MDIs may be phased out over the next 10-20 years.

Environmental effects of ozone depletion and its interactions with climate change: progress report, 2008.

PubMed

Andrady, Anthony; Aucamp, Pieter J; Bais, Alkiviadis; Ballaré, Carlos L; Björn, Lars Olof; Bornman, Janet F; Caldwell, Martyn; Cullen, Anthony P; Erickson, David J; de Gruijl, Frank R; Häder, Donat-P; Ilyas, Mohammad; Kulandaivelu, G; Kumar, H D; Longstreth, Janice; McKenzie, Richard L; Norval, Mary; Paul, Nigel; Redhwi, Halim Hamid; Smith, Raymond C; Solomon, Keith R; Sulzberger, Barbara; Takizawa, Yukio; Tang, Xiaoyan; Teramura, Alan H; Torikai, Ayako; van der Leun, Jan C; Wilson, Stephen R; Worrest, Robert C; Zepp, Richard G

2009-01-01

After the enthusiastic celebration of the 20th Anniversary of the Montreal Protocol on Substances that Deplete the Ozone Layer in 2007, the work for the protection of the ozone layer continues. The Environmental Effects Assessment Panel is one of the three expert panels within the Montreal Protocol. This EEAP deals with the increase of the UV irradiance on the Earth's surface and its effects on human health, animals, plants, biogeochemistry, air quality and materials. For the past few years, interactions of ozone depletion with climate change have also been considered. It has become clear that the environmental problems will be long-lasting. In spite of the fact that the worldwide production of ozone depleting chemicals has already been reduced by 95%, the environmental disturbances are expected to persist for about the next half a century, even if the protective work is actively continued, and completed. The latest full report was published in Photochem. Photobiol. Sci., 2007, 6, 201-332, and the last progress report in Photochem. Photobiol. Sci., 2008, 7, 15-27. The next full report on environmental effects is scheduled for the year 2010. The present progress report 2008 is one of the short interim reports, appearing annually.

Quantitative analysis of interaction between the free troposphere and planetary boundary layer using multiple measurements and large eddy simulation model

NASA Astrophysics Data System (ADS)

Huang, Guanyu

We investigate the interaction between the free troposphere (FT) and planetary boundary layer (PBL) using multiple measurements and Dutch Atmospheric Large Eddy Simulation (DALES) coupled with a chemical module. A residual layer (RL) storing high ozone concentrations can significantly influence ground ozone concentration through the entrainment process whereby the RL aloft is incorporated into the growing convective boundary layer (CBL) during the morning transition. We use DALES model coupled with a chemical module to simultaneously study the dynamical and chemical impacts of a RL (200-1200 m above ground level (AGL)) on ground-level (0-200 m AGL) ozone concentrations. Four numerical experiments test these interactions: 1) a RL with high ozone (100 ppb); 2) a RL with low ozone (50 ppb); 3) no RL with high ozone above the NBL (100 ppb from 200-1200 m AGL); and 4) no RL with low ozone above the NBL (50 ppb). The results indicate that ozone stored in the RL can contribute up to 86% of the ozone concentration in the CBL during the following day in Case 1. Even in Case 2, 64% of the ozone in the developed CBL results from intrusions from the RL. Additionally, a RL also increases the enhancement rate of ozone in the CBL. Furthermore, we investigate the ozone diurnal variation on September 6, 2013 in Huntsville AL. The ozone variation in the CBL is mainly caused by local emissions due to the weather conditions being controlled by an anticyclonic system. The local chemical production contributes over 67% of the ozone enhancement in the CBL. The dynamical processes contribute the rest. The numerical experiments show good agreement with our ozone lidar observations. However, our simulation results and ozone lidar observations fail to reproduce a declining trend of surface ozone measured by an Environment Protection Agency (EPA) surface monitoring station that is 6 km south of our facilities, which is very likely due to the large ozone horizontal variation and the diurnal variation of ozone dry deposition under urban environment.

Monitoring of Observation Errors in the Assimilation of Satellite Ozone Data

NASA Technical Reports Server (NTRS)

Stajner, Ivanka; Winslow, Nathan; Rood, Richard B.; Pawson, Steven

2003-01-01

The stratospheric ozone layer protects life on Earth from the harmful effects of solar ultravioiet radiation. The ozone layer is currently in a fragile state because of depletion caused by man-made chemicals, especially chlorofluorocarbons. The state of the ozone layer is being monitored and evaluated by scientific experts around the world, in order to help policy makers assess the impacts of international protocols that control the production and release of ozone depleting chemicals. Scientists use a variety ozone measurements and models in order to form a comprehensive picture about the current state of the ozone layer, and to predict the future behavior (expected to be a recovery, as the abundance of the depleting chemicals decreases). Among the data sets used, those from satellite-borne instruments have the advantage of providing a wealth of information about the ozone distribution over most of the globe. Several instruments onboard American and international satellites make measurements of the properties of the atmosphere, from which atmospheric ozone amounts are estimated; long-term measurement programs enable monitoring of trends in ozone. However, the characteristics of satellite instruments change in time. For example, the instrument lenses through which measurements are made may deteriorate over time, or the satellite orbit may drift so that measurements over each location are made later and later in the day. These changes may increase the errors in the retrieved ozone amounts, and degrade the quality of estimated ozone amounts and of their variability. Our work focuses on combining the satellite ozone data with global models that capture atmospheric motion and ozone chemistry, using advanced statistical techniques: this is known as data assimilation. Our method provides a three-dimensional global ozone distribution that is consistent with both the satellite measurements and with our understanding of processes (described in the models) that control ozone distribution. Through the monitoring of statistical properties of the agreement between the data and the model, this approach also enables us to detect changes in the quality of ozone data retrieved from satellite-borne instrument measurements. This paper demonstrates that calculations of the changes in satellite data quality, and the impact these changes on the estimates of the global ozone distribution, can assist in maintaining the uniform quality of the satellite ozone data throughout the lifetime of these instruments, thus contributing to our understanding of long-term ozone change.

Find RAD Partner Programs

EPA Pesticide Factsheets

RAD partner programs help protect the ozone layer and reduce emissions of greenhouse gases by disposing of older, inefficient refrigerated appliances using the best environmental practices and technologies available.

Find Recycling Facilities Servicing RAD Partners

EPA Pesticide Factsheets

RAD partners help protect the ozone layer and reduce emissions of greenhouse gases by disposing of older, inefficient refrigerated appliances using the best environmental practices and technologies available.

Fiber-Optic Coupled Lidar Receiver System to Measure Stratospheric Ozone

NASA Technical Reports Server (NTRS)

Harper, David Brent; Elsayed-Ali, Hani

1998-01-01

The measurement of ozone in the atmosphere has become increasingly important over the past two decades. Significant increases of ozone concentrations in the lower atmosphere, or troposphere, and decreases in the upper atmosphere, or stratosphere, have been attributed to man-made causes. High ozone concentrations in the troposphere pose a health hazard to plants and animals and can add to global warming. On the other hand, ozone in the stratosphere serves as a protective barrier against strong ultraviolet (UV) radiation from the sun. Man-made CFC's (chlorofluorocarbons) act as a catalyst with a free oxygen atom and an ozone molecule to produce two oxygen molecules therefore depleting the protective layer of ozone in the stratosphere. The beneficial and harmful effects of ozone require the study of ozone creation and destruction processes in the atmosphere. Therefore, to provide an accurate model of these processes, an ozone lidar system must be able to be used frequently with as large a measurement range as possible. Various methods can be used to measure atmospheric ozone concentrations. These include different airborne and balloon measurements, solar occulation satellite techniques, and the use of lasers in lidar (high detection and ranging,) systems to probe the atmosphere. Typical devices such as weather balloons can only measure within the direct vicinity of the instrument and are therefore used infrequently. Satellites use solar occulation techniques that yield low horizontal and vertical resolution column densities of ozone.

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.…

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.

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 incremental costs are indicated.

Stratospheric ozone measurements at Arosa (Switzerland): history and scientific relevance

NASA Astrophysics Data System (ADS)

Staehelin, Johannes; Viatte, Pierre; Stübi, Rene; Tummon, Fiona; Peter, Thomas

2018-05-01

Climatic Observatory (LKO) in Arosa (Switzerland), marking the beginning of the world's longest series of total (or column) ozone measurements. They were driven by the recognition that atmospheric ozone is important for human health, as well as by scientific curiosity about what was, at the time, an ill characterised atmospheric trace gas. From around the mid-1950s to the beginning of the 1970s studies of high atmosphere circulation patterns that could improve weather forecasting was justification for studying stratospheric ozone. In the mid-1970s, a paradigm shift occurred when it became clear that the damaging effects of anthropogenic ozone-depleting substances (ODSs), such as long-lived chlorofluorocarbons, needed to be documented. This justified continuing the ground-based measurements of stratospheric ozone. Levels of ODSs peaked around the mid-1990s as a result of a global environmental policy to protect the ozone layer, implemented through the 1987 Montreal Protocol and its subsequent amendments and adjustments. Consequently, chemical destruction of stratospheric ozone started to slow around the mid-1990s. To some extent, this raises the question as to whether continued ozone observation is indeed necessary. In the last decade there has been a tendency to reduce the costs associated with making ozone measurements globally including at Arosa. However, the large natural variability in ozone on diurnal, seasonal, and interannual scales complicates the capacity for demonstrating the success of the Montreal Protocol. Chemistry-climate models also predict a super-recovery of the ozone layer at mid-latitudes in the second half of this century, i.e. an increase of ozone concentrations beyond pre-1970 levels, as a consequence of ongoing climate change. These factors, and identifying potentially unexpected stratospheric responses to climate change, support the continued need to document stratospheric ozone changes. This is particularly valuable at the Arosa site, due to the unique length of the observational record. This paper presents the evolution of the ozone layer, the history of international ozone research, and discusses the justification for the measurements in the past, present and into future.

Reducing nitrous oxide emissions to mitigate climate change and protect the ozone layer.

PubMed

Li, Li; Xu, Jianhua; Hu, Jianxin; Han, Jiarui

2014-05-06

Reducing nitrous oxide (N2O) emissions offers the combined benefits of mitigating climate change and protecting the ozone layer. This study estimates historical and future N2O emissions and explores the mitigation potential for China's chemical industry. The results show that (1) from 1990 to 2012, industrial N2O emissions in China grew by some 37-fold from 5.07 to 174 Gg (N2O), with total accumulated emissions of 1.26 Tg, and (2) from 2012 to 2020, the projected emissions are expected to continue growing rapidly from 174 to 561 Gg under current policies and assuming no additional mitigation measures. The total accumulated mitigation potential for this forecast period is about 1.54 Tg, the equivalent of reducing all the 2011 greenhouse gases from Australia or halocarbon ozone-depleting substances from China. Adipic acid production, the major industrial emission source, contributes nearly 80% of the industrial N2O emissions, and represents about 96.2% of the industrial mitigation potential. However, the mitigation will not happen without implementing effective policies and regulatory programs.

Annual and Seasonal Global Variation in Total Ozone and Layer-Mean Ozone, 1958-1987 (1991)

DOE Office of Scientific and Technical Information (OSTI.GOV)

Angell, J. K.; Korshover, J.; Planet, W. G.

For 1958 through 1987, this data base presents total ozone variations and layer mean ozone variations expressed as percent deviations from the 1958 to 1977 mean. The total ozone variations were derived from mean monthly ozone values published in Ozone Data for the World by the Atmospheric Environment Service in cooperation with the World Meteorological Organization. The layer mean ozone variations are derived from ozonesonde and Umkehr observations. The data records include year, seasonal and annual total ozone variations, and seasonal and annual layer mean ozone variations. The total ozone data are for four regions (Soviet Union, Europe, North America,more » and Asia); five climatic zones (north and south polar, north and south temperate, and tropical); both hemispheres; and the world. Layer mean ozone data are for four climatic zones (north and south temperate and north and south polar) and for the stratosphere, troposphere, and tropopause layers. The data are in two files [seasonal and year-average total ozone (13.4 kB) and layer mean ozone variations (24.2 kB)].« less

Snapshot of the Antarctic Ozone Hole 2010

NASA Image and Video Library

2017-12-08

Image acquired September 12, 2010 The yearly depletion of stratospheric ozone over Antarctica – more commonly referred to as the “ozone hole” – started in early August 2010 and is now expanding toward its annual maximum. The hole in the ozone layer typically reaches its maximum area in late September or early October, though atmospheric scientists must wait a few weeks after the maximum to pinpoint when the trend of ozone depletion has slowed down and reversed. The hole isn’t literal; no part of the stratosphere — the second layer of the atmosphere, between 8 and 50 km (5 and 31 miles) — is empty of ozone. Scientists use "hole" as a metaphor for the area in which ozone concentrations drop below the historical threshold of 220 Dobson Units. Historical levels of ozone were much higher than 220 Dobson Units, according to NASA atmospheric scientist Paul Newman, so this value shows a very large ozone loss. Earth's ozone layer protects life by absorbing ultraviolet light, which damages DNA in plants and animals (including humans) and leads to skin cancer. The Ozone Monitoring Instrument (OMI) on NASA’s Aura satellite acquired data for this map of ozone concentrations over Antarctica on September 12, 2010. OMI is a spectrometer that measures the amount of sunlight scattered by Earth’s atmosphere and surface, allowing scientists to assess how much ozone is present at various altitudes — particularly the stratosphere — and near the ground. So far in 2010, the size and depth of the ozone hole has been slightly below the average for 1979 to 2009, likely because of warmer temperatures in the stratosphere over the far southern hemisphere. However, even slight changes in the meteorology of the region this month could affect the rate of depletion of ozone and how large an area the ozone hole might span. You can follow the progress of the ozone hole by visiting NASA’s Ozone Hole Watch page. September 16 is the International Day for the Preservation of the Ozone Layer, a commemoration of the day in 1987 when nations commenced the signing of the Montreal Protocol to limit and eventually ban ozone-depleting substances such as chlorofluorocarbons (CFCs) and other chlorine and bromine-containing compounds. The ozone scientific assessment panel for the United Nations Environment Program, which monitors the effectiveness of the Montreal Protocol, is expected to release its latest review of the state of the world’s ozone layer by the end of 2010. (The last assessment was released in 2006.) Paul Newman is one of the four co-chairs of the assessment panel. NASA image courtesy Ozone Hole Watch. Caption by Michael Carlowicz. Instrument: Aura - OMI To learn more go to: ozonewatch.gsfc.nasa.gov/ Credit: NASA’s Earth Observatory NASA Goddard Space Flight Center is home to the nation's largest organization of combined scientists, engineers and technologists that build spacecraft, instruments and new technology to study the Earth, the sun, our solar system, and the universe. Follow us on Twitter Join us on Facebook

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

An Application of spectral analysis method investigating the anomalous change in the QBO for period of 1997 to 2017, especially at 50 hPa related to the ozone’s concentration

NASA Astrophysics Data System (ADS)

Hermawan, Eddy

2018-05-01

This study is mainly concerned an application of the spectral tehnique analysis in investigating the anomalous change of the Quasi-Biennial Oscillation (QBO) over the equatorial region, especially over the Singapore related to the ozone’s concentration at about 50 hPa. This is important since we need to know that characteristics of ozone concentration at that layer due to the ozone depletion caused by the effect of the global warming. Please note here, ozone is already stated as one of the most important parameter needed to protect our earth from Ultra Violet (UV) light. No much study of ozone’s protection, especially near the equatorial region. In this preliminary results, we show the characteristics of QBO taken from the Singapore ‘s QBO data analysis. The QBO has represented as the downward propagating of zonal wind variation. Then, we investigate impact of QBO on the Ozone’s Concentration anomaly at stratospheric layer. We found the pre-dominant peak oscillation of QBO at around 28 month. We found also an a good agreement (pattern) between QBO and Ozone’s Concentration anomaly, especially at 50 hPa layer with a correlation coefficien of about 0.5. By this formula, we can estimate the next behavior of ozone’s concentration anomaly taken from the QBO index that updated regularly.

Clean Air Act Text

EPA Pesticide Factsheets

The Clean Air Act is the law that defines EPA's responsibilities for protecting and improving the nation's air quality and the stratospheric ozone layer. The last major change in the law, the Clean Air Act Amendments of 1990, enacted in 1990 by Congress.

Clean Air Act Requirements and History

EPA Pesticide Factsheets

In 1970 congress designed the Clean Air Act to combat a variety of air pollution problems, and to tackle emerging pollution threats such as public health, national welfare, toxic air pollutants, acid rain, protection of the ozone layer, and regional haze.

Attempts to probe the ozone layer and the ultraviolet-B levels of the past.

PubMed

Björn, Lars Olof; McKenzie, Richard L

2007-07-01

To get a proper perspective on the current status of atmospheric ozone, which protects the biosphere from ultraviolet-B (UV-B; 280-315 nm) radiation, it would be of value to know how ozone and UV-B radiation have varied in the past. The record of worldwide ozone monitoring goes back only a few decades, and the record of reliable UV-B measurements is even shorter. Here we review indirect methods to assess their status further back in time. These include variations in the Sun's emission and how these affect the atmosphere, changes in the Earth's orbit, geologic imprints of atmospheric ozone, effects of catastrophic events such as volcanic eruptions, biological proxies of UV-B radiation, the spectral signature of terrestrial ozone in old recordings of star spectra, and the modeling of UV-B irradiance from ozone data and meteorological recordings. Although reliable reconstructions do not yet extend far into the past, there is some hope for future progress.

Stratospheric ozone, global warming, and the principle of unintended consequences--an ongoing science and policy success story.

PubMed

Andersen, Stephen O; Halberstadt, Marcel L; Borgford-Parnell, Nathan

2013-06-01

In 1974, Mario Molina and F. Sherwood Rowland warned that chlorofluorocarbons (CFCs) could destroy the stratospheric ozone layer that protects Earth from harmful ultraviolet radiation. In the decade after scientists documented the buildup and long lifetime of CFCs in the atmosphere; found the proof that CFCs chemically decomposed in the stratosphere and catalyzed the depletion of ozone; quantified the adverse effects; and motivated the public and policymakers to take action. In 1987, 24 nations plus the European Community signed the Montreal Protocol. Today, 25 years after the Montreal Protocol was agreed, every United Nations state is a party (universal ratification of 196 governments); all parties are in compliance with the stringent controls; 98% of almost 100 ozone-depleting chemicals have been phased out worldwide; and the stratospheric ozone layer is on its way to recovery by 2065. A growing coalition of nations supports using the Montreal Protocol to phase down hydrofluorocarbons, which are ozone safe but potent greenhouse gases. Without rigorous science and international consensus, emissions of CFCs and related ozone-depleting substances (ODSs) could have destroyed up to two-thirds of the ozone layer by 2065, increasing the risk of causing millions of cancer cases and the potential loss of half of global agricultural production. Furthermore, because most, ODSs are also greenhouse gases, CFCs and related ODSs could have had the effect of the equivalent of 24-76 gigatons per year of carbon dioxide. This critical review describes the history of the science of stratospheric ozone depletion, summarizes the evolution of control measures and compliance under the Montreal Protocol and national legislation, presents a review of six separate transformations over the last 100 years in refrigeration and air conditioning (A/C) technology, and illustrates government-industry cooperation in continually improving the environmental performance of motor vehicle A/C.

Stratospheric ozone, global warming, and the principle of unintended consequences-An ongoing science and policy success story.

PubMed

Andersen, Stephen O; Halberstadt, Marcel L; Borgford-Parnell, Nathan

2013-06-01

In 1974, Mario Molina and F. Sherwood Rowland warned that chlorofluorocarbons (CFCs) could destroy the stratospheric ozone layer that protects Earth from harmful ultraviolet radiation. In the decade after, scientists documented the buildup and long lifetime of CFCs in the atmosphere; found the proof that CFCs chemically decomposed in the stratosphere and catalyzed the depletion of ozone; quantified the adverse effects; and motivated the public and policymakers to take action. In 1987, 24 nations plus the European Community signed the Montreal Protocol. Today, 25 years after the Montreal Protocol was agreed, every United Nations state is a party (universal ratification of 196 governments); all parties are in compliance with the stringent controls; 98% of almost 100 ozone-depleting chemicals have been phased out worldwide; and the stratospheric ozone layer is on its way to recovery by 2065. A growing coalition of nations supports using the Montreal Protocol to phase down hydrofluorocarbons, which are ozone safe but potent greenhouse gases. Without rigorous science and international consensus, emissions of CFCs and related ozone-depleting substances (ODSs) could have destroyed up to two-thirds of the ozone layer by 2065, increasing the risk of causing millions of cancer cases and the potential loss of half of global agricultural production. Furthermore, because most ODSs are also greenhouse gases, CFCs and related ODSs could have had the effect of the equivalent of 24-76 gigatons per year of carbon dioxide. This critical review describes the history of the science of stratospheric ozone depletion, summarizes the evolution of control measures and compliance under the Montreal Protocol and national legislation, presents a review of six separate transformations over the last 100 years in refrigeration and air conditioning (A/C) technology, and illustrates government-industry cooperation in continually improving the environmental performance of motor vehicle A/C. [Box: see text].

On the origin of regional spring time ozone episodes in the Western Mediterranean

NASA Astrophysics Data System (ADS)

Kalabokas, Pavlos; Hjorth, Jens; Foret, Gilles; Dufour, Gaëlle; Eremenko, Maxim; Siour, Guillaume; Cuesta, Juan; Beekmann, Matthias

2017-04-01

For the identification of regional spring time ozone episodes, rural EMEP ozone measurements from countries surrounding the Western Mediterranean (Spain, France, Switzerland, Italy, Malta) have been examined with emphasis on periods of high ozone, according to the daily variation of the afternoon (12:00 - 18:00) ozone. For two selected high ozone episodes in April-May 2008, composite NCEP/NCAR reanalysis maps of various meteorological parameters and/or their anomalies (geopotential height, specific humidity, vertical velocity omega, vector wind speed and temperature) at various tropospheric pressure levels have been examined together with the corresponding satellite IASI ozone measurements (at 3 and 10 km), CHIMERE simulations, vertical ozone soundings and HYSPLIT back trajectories (Kalabokas et al., 2016). The results show that high surface ozone is measured at several countries simultaneously over several days. Also, the examined spring ozone episodes in Western Mediterranean and Central Europe are linked to synoptic meteorological conditions very similar to those recently observed in summertime ozone episodes over the Eastern Mediterranean (Doche et al., 2014; Kalabokas et al., 2015 and references therein), where the transport of tropospheric ozone-rich air masses through atmospheric subsidence influences significantly the boundary layer and surface ozone concentrations. In particular, the geographic areas with observed tropospheric subsidence seem to be the transition regions between high pressure and low pressure systems. IASI satellite measurements show extended areas of high tropospheric ozone over the low pressure systems adjacent to the anticyclones, which influence significantly the boundary layer and surface ozone concentrations within the anticyclones by subsidence and advection, in addition to the photochemically produced ozone there, resulting to exceedances of the 60 ppb standard for human health protection over extended geographical areas. References Doche, C., Dufour, G., Foret, G., Eremenko, M., Cuesta, J., Beekmann, M., and Kalabokas, P., 2014. Summertime tropospheric-ozone variability over the Mediterranean basin observed with IASI, Atmos. Chem. Phys., 14, 10589-10600. Kalabokas P. D., Thouret V., Cammas J.-P., Volz-Τhomas A., Boulanger D., Repapis C.C., 2015. The geographical distribution of meteorological parameters associated with high and low summer ozone levels in the lower troposphere and the boundary layer over the eastern Mediterranean (Cairo case), Tellus B, 67, 27853, http://dx.doi.org/10.3402/tellusb.v67.27853. Kalabokas P., J. Hjorth, G. Foret, G. Dufour, M. Eremenko, G. Siour, J. Cuesta, M. Beekmann, 2016. An investigation on the origin of regional spring time ozone episodes in the Western Mediterranean and Central Europe. Atmos. Chem. Phys. Discuss., doi:10.5194/acp-2016-615.

Characteristics of ozone vertical profile observed in the boundary layer around Beijing in autumn.

PubMed

Ma, Zhiqiang; Zhang, Xiaoling; Xu, Jing; Zhao, Xiujuan; Meng, Wei

2011-01-01

In the autumn of 2008, the vertical profiles of ozone and meteorological parameters in the low troposphere (0-1000 m) were observed at two sites around Beijing, specifically urban Nanjiao and rural Shangdianzi. At night and early morning, the lower troposphere divided into two stratified layers due to temperature inversion. Ozone in the lower layer showed a large gradient due to the titration of NO. Air flow from the southwest brought ozone-rich air to Beijing, and the ozone profiles were marked by a continuous increase in the residual layer at night. The accumulated ozone in the upper layer played an important role in the next day's surface peak ozone concentration, and caused a rapid increase in surface ozone in the morning. Wind direction shear and wind speed shear exhibited different influences on ozone profiles and resulted in different surface ozone concentrations in Beijing.

The importance of the Montreal Protocol in protecting climate.

PubMed

Velders, Guus J M; Andersen, Stephen O; Daniel, John S; Fahey, David W; McFarland, Mack

2007-03-20

The 1987 Montreal Protocol on Substances that Deplete the Ozone Layer is a landmark agreement that has successfully reduced the global production, consumption, and emissions of ozone-depleting substances (ODSs). ODSs are also greenhouse gases that contribute to the radiative forcing of climate change. Using historical ODSs emissions and scenarios of potential emissions, we show that the ODS contribution to radiative forcing most likely would have been much larger if the ODS link to stratospheric ozone depletion had not been recognized in 1974 and followed by a series of regulations. The climate protection already achieved by the Montreal Protocol alone is far larger than the reduction target of the first commitment period of the Kyoto Protocol. Additional climate benefits that are significant compared with the Kyoto Protocol reduction target could be achieved by actions under the Montreal Protocol, by managing the emissions of substitute fluorocarbon gases and/or implementing alternative gases with lower global warming potentials.

The importance of the Montreal Protocol in protecting climate

PubMed Central

Velders, Guus J. M.; Andersen, Stephen O.; Daniel, John S.; Fahey, David W.; McFarland, Mack

2007-01-01

The 1987 Montreal Protocol on Substances that Deplete the Ozone Layer is a landmark agreement that has successfully reduced the global production, consumption, and emissions of ozone-depleting substances (ODSs). ODSs are also greenhouse gases that contribute to the radiative forcing of climate change. Using historical ODSs emissions and scenarios of potential emissions, we show that the ODS contribution to radiative forcing most likely would have been much larger if the ODS link to stratospheric ozone depletion had not been recognized in 1974 and followed by a series of regulations. The climate protection already achieved by the Montreal Protocol alone is far larger than the reduction target of the first commitment period of the Kyoto Protocol. Additional climate benefits that are significant compared with the Kyoto Protocol reduction target could be achieved by actions under the Montreal Protocol, by managing the emissions of substitute fluorocarbon gases and/or implementing alternative gases with lower global warming potentials. PMID:17360370

75 FR 53739 - Proposed Collection; Comment Request for Regulation Project

Federal Register 2010, 2011, 2012, 2013, 2014

2010-09-01

... the Ozone Layer; Special Rules for Certain Medical Uses of Chemicals That Deplete the Ozone Layer (Sec....gov . SUPPLEMENTARY INFORMATION: Title: Exports of Chemicals That Deplete the Ozone Layer; Special Rules for Certain Medical Uses of Chemicals That Deplete the Ozone Layer. OMB Number: 1545-1361...

Total ozone trend over Cairo

NASA Technical Reports Server (NTRS)

Hassan, G. K. Y.

1994-01-01

A world wide interest in protecting ozone layer against manmade effects is now increasing. Assessment of the ozone depletion due to these activities depends on how successfully we can separate the natural variabilities from the data. The monthly mean values of total ozone over Cairo (30 05N) for the period 1968-1988, have been analyzed using the power spectral analysis technique. The technique used in this analysis does not depend on a pre-understanding of the natural fluctuations in the ozone data. The method depends on increasing the resolution of the spectral peaks in order to obtain the more accurate sinusoidal fluctuations with wavelength equal to or less than record length. Also it handles the possible sinusoidal fluctuations with wavelength equal to or less than record length. The results show that it is possible to detect some of the well known national fluctuations in the ozone record such as annual, semiannual, quasi-biennial and quasi-quadrennial oscillations. After separating the natural fluctuations from the ozone record, the trend analysis of total ozone over Cairo showed that a decrease of about -1.2% per decade has occurred since 1979.

Selective sensing of ozone and the chemically active gaseous species of the troposphere by using the C20 fullerene and graphene segment.

PubMed

Vessally, Esmail; Siadati, Seyyed Amir; Hosseinian, Akram; Edjlali, Ladan

2017-01-01

OZONE is a key species in forming a layer in the atmosphere of earth that brings vita for our planet and supports the complex life. This three-atom molecule in the ozone-layer, is healing the earth's ecosystem by protecting it from dangerous rays of the sun. Until this molecule is in the stratosphere, it would support the natural order of the life; but, when it appears in our environment, damages will begin against us. In this project, we have tried to find a new way for beaconing ozone species in our environment via physical adsorption by the C 20 fullerene and graphene segment as a sensor. To find the selectivity of this nano-sized segment in sensing ozone (O 3 ), compared to the usual chemically active gasses of the troposphere like O 2 , N 2 , CO 2 , H 2 O, CH 4 , H 2 , and CO, the density of state (DOS) plots were analyzed, for each interacting species. The results showed that ozone could significantly change the electrical conductivity of C 20 fullerene, for each adsorption step. Thus, this fullerene could clearly sense ozone in different adsorption steps; while, the graphene segment could do this only at the second step adsorption (/ΔE g-B /=0.016eV) (at the first adsorption step the /ΔE g-A / is 0.00eV). Copyright © 2016 Elsevier B.V. All rights reserved.

A comparison of SAGE 1, SBUV, and Umkehr ozone profiles including a search for Umkehr aerosol effects

NASA Technical Reports Server (NTRS)

Newchurch, M. J.; Grams, G. W.; Cunnold, D. M.; Deluisi, J. J.

1987-01-01

Using a spatially weighted average for the stratospheric aerosol and gas experiment 1 (SAGE 1) events derived from an autocorrelation analysis, 337 colocated SAGE 1 and Umkehr ozone profiles are found. The total column ozone in layers two through nine measured by SAGE 1 is found to be 4.6 + or - 1.3 percent higher at the 95 percent confidence level than the approximate total column ozone measured by Umkehr. Average layer ozone differences indicate that most of this discrepancy resides in the lower layers. Intercomparison of SAGE 1, Nimbus 7 solar backscattered ultraviolet (SBUV), and Umkehr ozone at stations north of 30 deg indicates that, in layer six, Umkehr values are consistently higher than both SAGE 1 and SBUV by about 10 percent. In layer eight, SBUV ozone is higher than both SAGE 1 and SBUV by about 10 percent. In the upper stratosphere, the SAGE 1-Umkehr ozone differences are small for low stratospheric aerosol optical depth cases, but vary from -3 percent in layer six to -8 percent in layer nine for high optical depth cases.

Basic Ozone Layer Science

EPA Pesticide Factsheets

Learn about the ozone layer and how human activities deplete it. This page provides information on the chemical processes that lead to ozone layer depletion, and scientists' efforts to understand them.

[Responses of rice growth and development to elevated near-surface layer ozone (O3) concentration: a review].

PubMed

Yang, Lian-xin; Wang, Yu-long; Shi, Guang-yao; Wang, Yun-xia; Zhu, Jian-guo

2008-04-01

Ozone (O3) is recognized as one of the most important air pollutants. At present, the worldwide average tropospheric O3 concentration has been increased from an estimated pre-industrial level of 38 nl L(-1) (25-45 nl L(-1), 8-h summer seasonal average) to approximately 50 nl L(-1) in 2000, and to 80 nl L(-1) by 2100 based on most pessimistic projections. Oryza sativa L. (rice) is the most important grain crop in the world, and thus, to correctly evaluate how the elevated near-surface layer O3 concentration will affect the growth and development of rice is of great significance. This paper reviewed the chamber (including closed and open top chamber)-based studies about the effects of atmospheric ozone enrichment on the rice visible injury symptoms, photosynthesis, water relationship, phenology, dry matter production and allocation, leaf membrane protective system, and grain yield and its components. Further research directions in this field were discussed.

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…

Photoreactivation in Paramecium tetraurelia under conditions of various degrees of ozone layer depletion.

PubMed

Takahashi, Akihisa; Kumatani, Toshihiro; Usui, Saori; Tsujimura, Ryoko; Seki, Takaharu; Morimoto, Kouichi; Ohnishi, Takeo

2005-01-01

Photoreactivation (PR) is an efficient survival mechanism that helps protect cells against the harmful effects of solar-ultraviolet (UV) radiation. The PR mechanism involves photolyase, just one enzyme, and can repair DNA damage, such as cyclobutane-pyrimidine dimers (CPD) induced by near-UV/blue light, a component of sunlight. Although the balance of near-UV/blue light and far-UV light reaching the Earth's surface could be altered by the atmospheric ozone layer's depletion, experiments simulating this environmental change and its possible effects on life have not yet been performed. To quantify the strength of UVB in sunlight reaching the Earth's surface, we measured the number of CPD generated in plasmid DNA after UVB irradiation or exposure to sunlight. To simulate the increase of solar-UV radiation resulting from the ozone layer depletion, Paramecium tetraurelia was exposed to UVB and/or sunlight in clear summer weather. PR recovery after exposure to sunlight was complete at a low dose rate of 0.2 J/m2 x s, but was less efficient when the dose rate was increased by a factor of 2.5 to 0.5 J/m2 x s. It is suggested that solar-UV radiation would not influence the cell growth of P. tetraurelia for the reason of high PR activity even when the ozone concentration was decreased 30% from the present levels.

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)

Life and the solar uv environment on the early Earth

NASA Astrophysics Data System (ADS)

Bérces, A.; Kovács, G.; Rontó, G.; Lammer, H.; Kargl, G.; Kömle, N.; Bauer, S.

2003-04-01

The solar UV radiation environment on planetary surfaces and within their atmospheres is of importance in a wide range of scientific disciplines. Solar UV radiation is the driving force of chemical and organic evolution and serves also as a constraint in biological evolution. Studies of the solar UV environment of the early Earth 2.0 Gyr to 3.8 Gyr ago suggest that the terrestrial atmosphere was essentially anoxic, resulting in an ozone column abundance insufficient for protecting the planetary surface in the UV-B and the UV-C ranges. Since, short wavelength solar UV radiation in the UV-B ind UV-C range penetrated through the unprotected atmosphere to the surface on early Earth, associated biological consequences may be expected. For DNA-based terrestrial solar UV dosimetry, bacteriophage T7, isolated phage-DNA ind polycrystalline Uracil samples have been used. The effect of solar UV radiation can be measured by detecting the biological-structural consequences of the damage induced by UV photons. We show model calculations for the Biological Effective Dose (BED) rate of Uracil and bacteriophage T7, for various ozone concentrations representing early atmospheric conditions on Earth up to a UV protecting ozone layer comparable to present times. Further, we discuss experimental data which show the photo-reverse effect of Uracil molecules caused by short UV wavelengths. These photoreversion effect highly depend on the wavelength of the radiation. Shorter wavelength UV radiation of about 200 nm is strongly effective in monomerisation, while the longer wavelengths prefer the production of dimerisation. We could demonstrate experimentally, for the case of an Uracil thin-layer that the photo-reaction process of the nucleotides can be both, dimerization and the reverse process: monomerization. These results are important for the study of solar UV exposure on organisms in the terrestrial environment more than 2 Gyr ago where Earth had no UV protecting ozone layer as well as for the search for life on Mars since we can show that biological harmful effects can also be reduced by shorter wavelength UV radiation, which is of importance in reducing DNA damages provoked by wavelengths longer than about 240 nm.

Rapid vertical trace gas transport by an isolated midlatitude thunderstorm

NASA Astrophysics Data System (ADS)

Hauf, Thomas; Schulte, Peter; Alheit, Reiner; Schlager, Hans

1995-11-01

During the cloud dynamics and chemistry field experiment CLEOPATRA in the summer of 1992 in southern Germany, the Deutsche Forschungsanstalt für Luft- und Raumfahrt (DLR) (German Aerospace Research Establishment) research aircraft Falcon traversed four times the anvil of a severe, isolated thunderstorm. The first two traverses were at 8 km altitude and close to the anvil cloud base, while the second two traverses were at 10 km. During the 8-km traverse, measured ozone mixing ratios dropped by 13 parts per billion by volume (ppbv) from the ambient cloud free environment to the anvil cloud, while water vapor increased by 0.3 g kg-1. At the 10-km traverses, ozone dropped by 25 ppbv, while water vapor increased by 0.18 g kg-1. Three-dimensional numerical thunderstorm simulations were performed to understand the cause of these changes. The simulations included the transport of two chemical inert tracers. Ozone was assumed to be one of them. The initial ozone profile was composed from an ozone routine sounding and the in situ Falcon measurements prior to the thunderstorm development. The second tracer is typical for a surface released pollutant with a nonzero, constant value in the boundary layer but zero above it. The redistribution of both tracers by the storm is calculated and compared with the observations. For the anvil penetration at 10 km, the calculated difference in ozone mixing ratios is 21 ppbv, while for water vapor an increase of 0.25 g kg-1 was found, in good agreement with the observations. To validate the model results, the radar reflectivity was calculated from simulated fields of cloud water, rain, graupel, hail, and snow and ice crystals and compared with observed values. With respect to maximum reflectivity values and spatial scales, again, excellent agreement was achieved. It is concluded that the rapid transport from the boundary layer directly into the anvil level is the most likely cause of the observed ozone decrease and water vapor increase. Entrainment of ozone-rich environmental air into the anvil cloud occurred but left a protected core with undiluted boundary layer air in the anvil cloud even at a distance of 120 km from the main updraft. Processes such as production of O3 by electrical discharges, chemical reactions of ozone with boundary layer-released or lightning-produced nitrogen compounds, scavenging by hydrometeors, and heterogeneous reactions at the surface of ice crystals may occur, but on the timescale of 0.5-1 hour seem to have a negligible influence on the observed ozone drop.

Children's and Adults' Knowledge and Models of Reasoning about the Ozone Layer and Its Depletion.

ERIC Educational Resources Information Center

Leighton, Jacqueline P.; Bisanz, Gay L.

2003-01-01

Examines children's and adults' knowledge of the ozone layer and its depletion, whether this knowledge increases with age, and how the ozone layer and ozone hole might be structured as scientific concepts. Uses a standardized set of questions to interview children and adults in Canada. Discusses implications of the results for health…

The reservoir of ozone in the boundary layer of the eastern United States and its potential impact on the global tropospheric ozone budget

NASA Technical Reports Server (NTRS)

Vukovich, F. M.; Fishman, J.; Browell, E. V.

1985-01-01

An analysis of available ozone data in the eastern two-thirds of the United States indicates that a substantial reservoir of ozone is present in the summertime. Five-year mean concentrations range from 40 to 65 ppbv. The reservoir covered an area of several million square kilometers and extends vertically from the surface to 1 to 2 km. The vertical distribution of ozone in the reservoir during midday supports a transport of additional ozone from the boundary layer to the free troposphere. Data are presented demonstrating the potential effect of transport by convective clouds and by the sea breeze circulation - mechanisms by which ozone may be transported out of the boundary layer into the free troposphere. The potential impact of this reservoir on the tropospheric ozone budget is discussed. It is shown that if less than half of the ozone mass in this reservoir is transported to the free troposphere, then the amount of ozone transported out of the boundary layer approximates the amount of ozone transported downward during a tropopause fold event.

Boundary layer ozone - An airborne survey above the Amazon Basin

NASA Technical Reports Server (NTRS)

Gregory, Gerald L.; Browell, Edward V.; Warren, Linda S.

1988-01-01

Ozone data obtained over the forest canopy of the Amazon Basin during July and August 1985 in the course of NASA's Amazon Boundary Layer Experiment 2A are discussed, and ozone profiles obtained during flights from Belem to Tabatinga, Brazil, are analyzed to determine any cross-basin effects. The analyses of ozone data indicate that the mixed layer of the Amazon Basin, for the conditions of undisturbed meteorology and in the absence of biomass burning, is a significant sink for tropospheric ozone. As the coast is approached, marine influences are noted at about 300 km inland, and a transition from a forest-controlled mixed layer to a marine-controlled mixed layer is noted.

Children's Use of Metaphors in Relation To Their Mental Models: The Case of the Ozone Layer and Its Depletion.

ERIC Educational Resources Information Center

Christidou, Vasilia; Koulaidis, Vasilis; Christidis, Theodor

1997-01-01

Examines the relationship between children's use of metaphors and their mental models concerning the ozone layer and ozone layer depletion. Results indicate that the way children represent the role and depletion of ozone is strongly correlated with the types of metaphors they use while constructing and/or articulating their models. Also discusses…

Vertical ozone characteristics in urban boundary layer in Beijing.

PubMed

Ma, Zhiqiang; Xu, Honghui; Meng, Wei; Zhang, Xiaoling; Xu, Jing; Liu, Quan; Wang, Yuesi

2013-07-01

Vertical ozone and meteorological parameters were measured by tethered balloon in the boundary layer in the summer of 2009 in Beijing, China. A total of 77 tethersonde soundings were taken during the 27-day campaign. The surface ozone concentrations measured by ozonesondes and TEI 49C showed good agreement, albeit with temporal difference between the two instruments. Two case studies of nocturnal secondary ozone maxima are discussed in detail. The development of the low-level jet played a critical role leading to the observed ozone peak concentrations in nocturnal boundary layer (NBL). The maximum of surface ozone was 161.7 ppbv during the campaign, which could be attributed to abundant precursors storage near surface layer at nighttime. Vertical distribution of ozone was also measured utilizing conventional continuous analyzers on 325-m meteorological observation tower. The results showed the NBL height was between 47 and 280 m, which were consistent with the balloon data. Southerly air flow could bring ozone-rich air to Beijing, and the ozone concentrations exceeded the China's hourly ozone standard (approximately 100 ppb) above 600 m for more than 12 h.

Urban and Rural Ozone Collect over Lusaka (Zambia, 15.5 S, 28 E) during SAFARI-2000 (September 2000)

NASA Technical Reports Server (NTRS)

Thompson, Anne M.; Witte, Jacquelyn C.; Freiman, M. Tai; Phalane, N. Agnes; Coetzee, Gert J. R.

2002-01-01

In early September, throughout south central Africa, seasonal clearing of dry vegetation and the production of charcoal for cooking leads to intense smoke haze and ozone formation. Ozone soundings made over Lusaka in early September 2000 recorded layers of high ozone (greater than 125 ppbv at 5 km) during two stagnant periods, broken by a frontal passage that reduced boundary layer ozone by 30%. During the 6-day measurement period, surface ozone concentrations ranged from 50-95 ppbv and integrated tropospheric ozone from the soundings was 39-54 Dobson Units (note 1.3 km elevation at the launch site). A stable layer of high ozone at 2-5 km was advected from rural burning regions in western Zambia and neighboring countries, making Lusaka a collection point for transboundary pollution. This is confirmed by trajectories that show ozone leaving Angola, Namibia, Botswana and South Africa before heading toward the Indian Ocean and returning to Lusaka via Mozambique and Zimbabwe. Ozone in the mixed layer at Lusaka is heavily influenced by local sources.

[Analysis on concentration variety characteristics of atmospheric ozone under the boundary layer in Beijing].

PubMed

Zong, Xue-Mei; Wang, Geng-Chen; Chen, Hong-Bin; Wang, Pu-Cai; Xuan, Yue-Jian

2007-11-01

Based on the atmospheric ozone sounding data, the average monthly and seasonal variety principles of atmospheric ozone concentration during six years are analyzed under the boundary layer in Beijing. The results show that the monthly variation of atmospheric ozone are obvious that the minimum values appear in January from less than 10 x 10(-9) on ground to less than 50 x 10(-9) on upper layer (2 km), but the maximum values appear in June from 85 x 10(-9) on ground to more than 90 x 10(-9) on upper layer. The seasonal variation is also clear that the least atmospheric ozone concentration is in winter and the most is in summer, but variety from ground to upper layer is largest in winter and least in summer. According to the type of outline, the outline of ozone concentration is composite of three types which are winter type, summer type and spring-autumn type. The monthly ozone concentration in different heights is quite different. After analyzing the relationship between ozone concentration and meteorological factors, such as temperature and humidity, we find ozone concentration on ground is linear with temperature and the correlation coefficient is more than 85 percent.

The Total Ozone Series of Arosa: History, Homogenization and new results using statistical extreme value theory

NASA Astrophysics Data System (ADS)

Staehelin, J.; Rieder, H. E.; Maeder, J. A.; Ribatet, M.; Davison, A. C.; Stübi, R.

2009-04-01

Atmospheric ozone protects the biota living at the Earth's surface from harmful solar UV-B and UV-C radiation. The global ozone shield is expected to gradually recover from the anthropogenic disturbance of ozone depleting substances (ODS) in the coming decades. The stratospheric ozone layer at extratropics might significantly increase above the thickness of the chemically undisturbed atmosphere which might enhance ozone concentrations at the tropopause altitude where ozone is an important greenhouse gas. At Arosa, a resort village in the Swiss Alps, total ozone measurements started in 1926 leading to the longest total ozone series of the world. One Fery spectrograph and seven Dobson spectrophotometers were operated at Arosa and the method used to homogenize the series will be presented. Due to its unique length the series allows studying total ozone in the chemically undisturbed as well as in the ODS loaded stratosphere. The series is particularly valuable to study natural variability in the period prior to 1970, when ODS started to affect stratospheric ozone. Concepts developed by extreme value statistics allow objective definitions of "ozone extreme high" and "ozone extreme low" values by fitting the (daily mean) time series using the Generalized Pareto Distribution (GPD). Extreme high ozone events can be attributed to effects of ElNino and/or NAO, whereas in the chemically disturbed stratosphere high frequencies of extreme low total ozone values simultaneously occur with periods of strong polar ozone depletion (identified by statistical modeling with Equivalent Stratospheric Chlorine times Volume of Stratospheric Polar Clouds) and volcanic eruptions (such as El Chichon and Pinatubo).

Children's Models of Understanding of Two Major Global Environmental Issues (Ozone Layer and Greenhouse Effect).

ERIC Educational Resources Information Center

Boyes, Edward; Stanisstreet, Martin

1997-01-01

Aims to quantify the models that 13- and 14 year-old students hold about the causes of the greenhouse effect and ozone layer depletion. Assesses the prevalence of those ideas that link the two phenomena. Twice as many students think that holes in the ozone layer cause the greenhouse effect than think the greenhouse effect causes ozone depletion.…

Experimental Determination of Ultraviolet Radiation Protection of Common Materials

ERIC Educational Resources Information Center

Tavares, Susana C. A.; da Silva, Joaquim C. G. Esteves; Paiva, Joao

2007-01-01

Aiming at a better understanding of the problems associated with the depletion of the ozone layer, we propose several experiments to be performed by students of different levels: secondary and first-year undergraduate students. The oxidation of iodide induced by ultraviolet (UV) radiation, generated by a mercury lamp, is used as an indicator for…

Survival of microorganisms in space protected by meteorite material: results of the experiment 'EXOBIOLOGIE' of the PERSEUS mission.

PubMed

Rettberg, P; Eschweiler, U; Strauch, K; Reitz, G; Horneck, G; Wanke, H; Brack, A; Barbier, B

2002-01-01

During the early evolution of life on Earth, before the formation of a protective ozone layer in the atmosphere, high intensities of solar UV radiation of short wavelengths could reach the surface of the Earth. Today the full spectrum of solar UV radiation is only experienced in space, where other important space parameters influence survival and genetic stability additionally, like vacuum, cosmic radiation, temperature extremes, microgravity. To reach a better understanding of the processes leading to the origin, evolution and distribution of life we have performed space experiments with microorganisms. The ability of resistant life forms like bacterial spores to survive high doses of extraterrestrial solar UV alone or in combination with other space parameters, e.g. vacuum, was investigated. Extraterrestrial solar UV was found to have a thousand times higher biological effectiveness than UV radiation filtered by stratospheric ozone concentrations found today on Earth. The protective effects of anorganic substances like artificial or real meteorites were determined on the MIR station. In the experiment EXOBIOLOGIE of the French PERSEUS mission (1999) it was found that very thin layers of anorganic material did not protect spores against the deleterious effects of energy-rich UV radiation in space to the expected amount, but that layers of UV radiation inactivated spores serve as a UV-shield by themselves, so that a hypothetical interplanetary transfer of life by the transport of microorganisms inside rocks through the solar system cannot be excluded, but requires the shielding of a substantial mass of anorganic substances. c2002 COSPAR. Published by Elsevier Science Ltd. All rights reserved.

Teaching about ozone layer depletion in Turkey: pedagogical content knowledge of science teachers.

PubMed

Bozkurt, Orçun; Kaya, Osman Nafiz

2008-04-01

The purpose of this study was to investigate the pedagogical content knowledge of Prospective Science Teachers (PSTs) on the topic of "ozone layer depletion." In order to explore PSTs' subject matter knowledge on ozone layer depletion, they were given a form of multiple-choice test where they needed to write the reasons behind their answers. This test was completed by 140 PSTs in their final year at the College of Education. Individual interviews were carried out with 42 randomly selected PSTs to determine their pedagogical knowledge about ozone layer depletion. Data were obtained from the study which indicate that the PSTs did not have adequate subject matter and pedagogical knowledge to teach the topic of ozone layer depletion to middle school students. It was also evident that the PSTs held various misconceptions related to ozone layer depletion. PSTs' inadequate pedagogical knowledge was found in the areas of the curriculum, learning difficulties of students, and instructional strategies and activities. This study provides some pedagogical implications for the training of science teachers.

Quantifying Ozone Production throughout the Boundary Layer from High Frequency Tethered Profile Measurements during a High Ozone Episode in the Uinta Basin, Utah

NASA Astrophysics Data System (ADS)

Sterling, C. W.; Johnson, B.; Schnell, R. C.; Oltmans, S. J.; Cullis, P.; Hall, E. G.; Jordan, A. F.; Windell, J.; McClure-Begley, A.; Helmig, D.; Petron, G.

2015-12-01

During the Uinta Basin Winter Ozone Study (UBWOS) in Jan - Feb 2013, 735 tethered ozonesonde profiles were obtained at 3 sites including during high wintertime photochemical ozone production events that regularly exceeded 125 ppb. High resolution profiles of ozone and temperature with altitude, measured during daylight hours, showed the development of approximately week long high ozone episodes building from background levels of ~40 ppb to >150 ppb. The topography of the basin combined with a strong temperature inversion trapped oil and gas production effluents in the basin and the snow covered surface amplified the sun's radiation driving the photochemical ozone production at rates up to 13 ppb/hour in a cold layer capped at 1600-1700 meters above sea level. Beginning in mid-morning, ozone mixing ratios throughout the cold layer increased until late afternoon. Ozone mixing ratios were generally constant with height indicating that ozone production was nearly uniform throughout the depth of the cold pool. Although there was strong diurnal variation, ozone mixing ratios increased during the day more than decreased during the night, resulting in elevated levels the next morning; an indication that nighttime loss processes did not compensate for daytime production. Even though the 3 tethersonde sites were at elevations differing by as much as 140 m, the top of the high ozone layer was nearly uniform in altitude at the 3 locations. Mobile van surface ozone measurements across the basin confirmed this capped structure of the ozone layer; the vehicle drove out of high ozone mixing ratios at an elevation of ~1900 meters above sea level, above which free tropospheric ozone mixing ratios of ~50 ppb were measured. Exhaust plumes from a coal-fired power plant in the eastern portion of the basin were intercepted by the tethersondes. The structure of the profiles clearly showed that effluents in the plumes were not mixed downward and thus did not contribute precursor nitrogen oxides to the observed ozone production in the boundary layer.

78 FR 39830 - Proposed Collection; Comment Request for Regulation Project

Federal Register 2010, 2011, 2012, 2013, 2014

2013-07-02

... excise tax on chemicals that deplete the ozone layer and on products containing such chemicals. DATES... the Ozone Layer and on Products Containing Such Chemicals. OMB Number: 1545-1153. Regulation Project... ozone layer and on products containing such chemicals. The regulation affects manufacturers and...

Entrainment of stratospheric air and Asian pollution by the convective boundary layer in the southwestern U.S.

NASA Astrophysics Data System (ADS)

Langford, A. O.; Alvarez, R. J.; Brioude, J.; Fine, R.; Gustin, M. S.; Lin, M. Y.; Marchbanks, R. D.; Pierce, R. B.; Sandberg, S. P.; Senff, C. J.; Weickmann, A. M.; Williams, E. J.

2017-01-01

A series of deep stratospheric intrusions in late May 2013 increased the daily maximum 8 h surface ozone (O3) concentrations to more than 70 parts per billion by volume (ppbv) at rural and urban surface monitors in California and Nevada. This influx of ozone-rich lower stratospheric air and entrained Asian pollution persisted for more than 5 days and contributed to exceedances of the 2008 8 h national ambient air quality standard of 75 ppbv on 21 and 25 May in Clark County, NV. Exceedances would also have occurred on 22 and 23 May had the new standard of 70 ppbv been in effect. In this paper, we examine this episode using lidar measurements from a high-elevation site on Angel Peak, NV, and surface measurements from NOAA, the Clark County, Nevada Department of Air Quality, the Environmental Protection Agency Air Quality System, and the Nevada Rural Ozone Initiative. These measurements, together with analyses from the National Centers for Environmental Prediction/North American Regional Reanalysis; NOAA Geophysical Fluid Dynamics Laboratory AM3 model; NOAA National Environmental Satellite, Data, and Information Service Real-time Air Quality Modeling System; and FLEXPART models, show that the exceedances followed entrainment of 20 to 40 ppbv of lower stratospheric ozone mingled with another 0 to 10 ppbv of ozone transported from Asia by the unusually deep convective boundary layers above the Mojave desert. Our analysis suggests that this vigorous mixing can affect both high and low elevations and help explain the springtime ozone maximum in the southwestern U.S.

Atomic layer deposition of a high-k dielectric on MoS2 using trimethylaluminum and ozone.

PubMed

Cheng, Lanxia; Qin, Xiaoye; Lucero, Antonio T; Azcatl, Angelica; Huang, Jie; Wallace, Robert M; Cho, Kyeongjae; Kim, Jiyoung

2014-08-13

We present an Al2O3 dielectric layer on molybdenum disulfide (MoS2), deposited using atomic layer deposition (ALD) with ozone/trimethylaluminum (TMA) and water/TMA as precursors. The results of atomic force microscopy and low-energy ion scattering spectroscopy show that using TMA and ozone as precursors leads to the formation of uniform Al2O3 layers, in contrast to the incomplete coverage we observe when using TMA/H2O as precursors. Our Raman and X-ray photoelectron spectroscopy measurements indicate minimal variations in the MoS2 structure after ozone treatment at 200 °C, suggesting its excellent chemical resistance to ozone.

Quantifying wintertime boundary layer ozone production from frequent profile measurements in the Uinta Basin, UT, oil and gas region

NASA Astrophysics Data System (ADS)

Schnell, Russell C.; Johnson, Bryan J.; Oltmans, Samuel J.; Cullis, Patrick; Sterling, Chance; Hall, Emrys; Jordan, Allen; Helmig, Detlev; Petron, Gabrielle; Ahmadov, Ravan; Wendell, James; Albee, Robert; Boylan, Patrick; Thompson, Chelsea R.; Evans, Jason; Hueber, Jacques; Curtis, Abigale J.; Park, Jeong-Hoo

2016-09-01

As part of the Uinta Basin Winter Ozone Study, January-February 2013, we conducted 937 tethered balloon-borne ozone vertical and temperature profiles from three sites in the Uinta Basin, Utah (UB). Emissions from oil and gas operations combined with snow cover were favorable for producing high ozone-mixing ratios in the surface layer during stagnant and cold-pool episodes. The highly resolved profiles documented the development of approximately week-long ozone production episodes building from regional backgrounds of 40 ppbv to >165 ppbv within a shallow cold pool up to 200 m in depth. Beginning in midmorning, ozone-mixing ratios increased uniformly through the cold pool layer at rates of 5-12 ppbv/h. During ozone events, there was a strong diurnal cycle with each succeeding day accumulating 4-8 ppbv greater than the previous day. The top of the elevated ozone production layer was nearly uniform in altitude across the UB independent of topography. Above the ozone production layer, mixing ratios decreased with height to 400 m above ground level where they approached regional background levels. Rapid clean-out of ozone-rich air occurred within a day when frontal systems brought in fresh air. Solar heating and basin topography led to a diurnal flow pattern in which daytime upslope winds distributed ozone precursors and ozone in the Basin. NOx-rich plumes from a coal-fired power plant in the eastern sector of the Basin did not appear to mix down into the cold pool during this field study.

Study of Ozone Layer Variability near St. Petersburg on the Basis of SBUV Satellite Measurements and Numerical Simulation (2000-2014)

NASA Astrophysics Data System (ADS)

Virolainen, Y. A.; Timofeyev, Y. M.; Smyshlyaev, S. P.; Motsakov, M. A.; Kirner, O.

2017-12-01

A comparison between the numerical simulation results of ozone fields with different experimental data makes it possible to estimate the quality of models for their further use in reliable forecasts of ozone layer evolution. We analyze time series of satellite (SBUV) measurements of the total ozone column (TOC) and the ozone partial columns in two atmospheric layers (0-25 and 25-60 km) and compare them with the results of numerical simulation in the chemistry transport model (CTM) for the low and middle atmosphere and the chemistry climate model EMAC. The daily and monthly average ozone values, short-term periods of ozone depletion, and long-term trends of ozone columns are considered; all data sets relate to St. Petersburg and the period between 2000 and 2014. The statistical parameters (means, standard deviations, variations, medians, asymmetry parameter, etc.) of the ozone time series are quite similar for all datasets. However, the EMAC model systematically underestimates the ozone columns in all layers considered. The corresponding differences between satellite measurements and EMAC numerical simulations are (5 ± 5)% and (7 ± 7)% and (1 ± 4)% for the ozone column in the 0-25 and 25-60 km layers, respectively. The correspondent differences between SBUV measurements and CTM results amount to (0 ± 7)%, (1 ± 9)%, and (-2 ± 8)%. Both models describe the sudden episodes of the ozone minimum well, but the EMAC accuracy is much higher than that of the CTM, which often underestimates the ozone minima. Assessments of the long-term linear trends show that they are close to zero for all datasets for the period under study.

Why do Models Overestimate Surface Ozone in the Southeastern United States?

NASA Technical Reports Server (NTRS)

Travis, Katherine R.; Jacob, Daniel J.; Fisher, Jenny A.; Kim, Patrick S.; Marais, Eloise A.; Zhu, Lei; Yu, Karen; Miller, Christopher C.; Yantosca, Robert M.; Sulprizio, Melissa P.;

Why do models overestimate surface ozone in the Southeast United States?

NASA Astrophysics Data System (ADS)

Travis, Katherine R.; Jacob, Daniel J.; Fisher, Jenny A.; Kim, Patrick S.; Marais, Eloise A.; Zhu, Lei; Yu, Karen; Miller, Christopher C.; Yantosca, Robert M.; Sulprizio, Melissa P.; Thompson, Anne M.; Wennberg, Paul O.; Crounse, John D.; St. Clair, Jason M.; Cohen, Ronald C.; Laughner, Joshua L.; Dibb, Jack E.; Hall, Samuel R.; Ullmann, Kirk; Wolfe, Glenn M.; Pollack, Illana B.; Peischl, Jeff; Neuman, Jonathan A.; Zhou, Xianliang

2016-11-01

Ozone pollution in the Southeast US involves complex chemistry driven by emissions of anthropogenic nitrogen oxide radicals (NOx ≡ NO + NO2) and biogenic isoprene. Model estimates of surface ozone concentrations tend to be biased high in the region and this is of concern for designing effective emission control strategies to meet air quality standards. We use detailed chemical observations from the SEAC4RS aircraft campaign in August and September 2013, interpreted with the GEOS-Chem chemical transport model at 0.25° × 0.3125° horizontal resolution, to better understand the factors controlling surface ozone in the Southeast US. We find that the National Emission Inventory (NEI) for NOx from the US Environmental Protection Agency (EPA) is too high. This finding is based on SEAC4RS observations of NOx and its oxidation products, surface network observations of nitrate wet deposition fluxes, and OMI satellite observations of tropospheric NO2 columns. Our results indicate that NEI NOx emissions from mobile and industrial sources must be reduced by 30-60 %, dependent on the assumption of the contribution by soil NOx emissions. Upper-tropospheric NO2 from lightning makes a large contribution to satellite observations of tropospheric NO2 that must be accounted for when using these data to estimate surface NOx emissions. We find that only half of isoprene oxidation proceeds by the high-NOx pathway to produce ozone; this fraction is only moderately sensitive to changes in NOx emissions because isoprene and NOx emissions are spatially segregated. GEOS-Chem with reduced NOx emissions provides an unbiased simulation of ozone observations from the aircraft and reproduces the observed ozone production efficiency in the boundary layer as derived from a regression of ozone and NOx oxidation products. However, the model is still biased high by 6 ± 14 ppb relative to observed surface ozone in the Southeast US. Ozonesondes launched during midday hours show a 7 ppb ozone decrease from 1.5 km to the surface that GEOS-Chem does not capture. This bias may reflect a combination of excessive vertical mixing and net ozone production in the model boundary layer.

Why do Models Overestimate Surface Ozone in the Southeastern United States?

PubMed

Travis, Katherine R; Jacob, Daniel J; Fisher, Jenny A; Kim, Patrick S; Marais, Eloise A; Zhu, Lei; Yu, Karen; Miller, Christopher C; Yantosca, Robert M; Sulprizio, Melissa P; Thompson, Anne M; Wennberg, Paul O; Crounse, John D; St Clair, Jason M; Cohen, Ronald C; Laughner, Joshua L; Dibb, Jack E; Hall, Samuel R; Ullmann, Kirk; Wolfe, Glenn M; Pollack, Illana B; Peischl, Jeff; Neuman, Jonathan A; Zhou, Xianliang

2016-01-01

Ozone pollution in the Southeast US involves complex chemistry driven by emissions of anthropogenic nitrogen oxide radicals (NO x ≡ NO + NO 2 ) and biogenic isoprene. Model estimates of surface ozone concentrations tend to be biased high in the region and this is of concern for designing effective emission control strategies to meet air quality standards. We use detailed chemical observations from the SEAC 4 RS aircraft campaign in August and September 2013, interpreted with the GEOS-Chem chemical transport model at 0.25°×0.3125° horizontal resolution, to better understand the factors controlling surface ozone in the Southeast US. We find that the National Emission Inventory (NEI) for NO x from the US Environmental Protection Agency (EPA) is too high. This finding is based on SEAC 4 RS observations of NO x and its oxidation products, surface network observations of nitrate wet deposition fluxes, and OMI satellite observations of tropospheric NO 2 columns. Our results indicate that NEI NO x emissions from mobile and industrial sources must be reduced by 30-60%, dependent on the assumption of the contribution by soil NO x emissions. Upper tropospheric NO 2 from lightning makes a large contribution to satellite observations of tropospheric NO 2 that must be accounted for when using these data to estimate surface NO x emissions. We find that only half of isoprene oxidation proceeds by the high-NO x pathway to produce ozone; this fraction is only moderately sensitive to changes in NO x emissions because isoprene and NO x emissions are spatially segregated. GEOS-Chem with reduced NO x emissions provides an unbiased simulation of ozone observations from the aircraft, and reproduces the observed ozone production efficiency in the boundary layer as derived from a regression of ozone and NO x oxidation products. However, the model is still biased high by 8±13 ppb relative to observed surface ozone in the Southeast US. Ozonesondes launched during midday hours show a 7 ppb ozone decrease from 1.5 km to the surface that GEOS-Chem does not capture. This bias may reflect a combination of excessive vertical mixing and net ozone production in the model boundary layer.

Why do Models Overestimate Surface Ozone in the Southeastern United States?

PubMed Central

Travis, Katherine R.; Jacob, Daniel J.; Fisher, Jenny A.; Kim, Patrick S.; Marais, Eloise A.; Zhu, Lei; Yu, Karen; Miller, Christopher C.; Yantosca, Robert M.; Sulprizio, Melissa P.; Thompson, Anne M.; Wennberg, Paul O.; Crounse, John D.; St Clair, Jason M.; Cohen, Ronald C.; Laughner, Joshua L.; Dibb, Jack E.; Hall, Samuel R.; Ullmann, Kirk; Wolfe, Glenn M.; Pollack, Illana B.; Peischl, Jeff; Neuman, Jonathan A.; Zhou, Xianliang

2018-01-01

Ozone pollution in the Southeast US involves complex chemistry driven by emissions of anthropogenic nitrogen oxide radicals (NOx ≡ NO + NO2) and biogenic isoprene. Model estimates of surface ozone concentrations tend to be biased high in the region and this is of concern for designing effective emission control strategies to meet air quality standards. We use detailed chemical observations from the SEAC4RS aircraft campaign in August and September 2013, interpreted with the GEOS-Chem chemical transport model at 0.25°×0.3125° horizontal resolution, to better understand the factors controlling surface ozone in the Southeast US. We find that the National Emission Inventory (NEI) for NOx from the US Environmental Protection Agency (EPA) is too high. This finding is based on SEAC4RS observations of NOx and its oxidation products, surface network observations of nitrate wet deposition fluxes, and OMI satellite observations of tropospheric NO2 columns. Our results indicate that NEI NOx emissions from mobile and industrial sources must be reduced by 30–60%, dependent on the assumption of the contribution by soil NOx emissions. Upper tropospheric NO2 from lightning makes a large contribution to satellite observations of tropospheric NO2 that must be accounted for when using these data to estimate surface NOx emissions. We find that only half of isoprene oxidation proceeds by the high-NOx pathway to produce ozone; this fraction is only moderately sensitive to changes in NOx emissions because isoprene and NOx emissions are spatially segregated. GEOS-Chem with reduced NOx emissions provides an unbiased simulation of ozone observations from the aircraft, and reproduces the observed ozone production efficiency in the boundary layer as derived from a regression of ozone and NOx oxidation products. However, the model is still biased high by 8±13 ppb relative to observed surface ozone in the Southeast US. Ozonesondes launched during midday hours show a 7 ppb ozone decrease from 1.5 km to the surface that GEOS-Chem does not capture. This bias may reflect a combination of excessive vertical mixing and net ozone production in the model boundary layer. PMID:29619045

Experimental Findings from Aircraft Measurements in the Residual Layer

NASA Astrophysics Data System (ADS)

Caputi, D.; Conley, S. A.; Faloona, I. C.; Trousdell, J.

2016-12-01

The southern San Joaquin Valley of California is home to some of the highest ozone pollution in the United States. Thus, a complete understanding of boundary layer dynamics in this area during high ozone events is crucial for better ozone forecasting and effective attainment planning. This work will discuss the results from five aircraft deployments, spanning two summers, in which a Mooney aircraft operated by Scientific Aviation Inc. was flown between Fresno and Bakersfield throughout the diurnal cycle, measuring ozone, NOx, and methane. Under a simple budgeting model, changes in any species within the boundary layer can occur from advection, chemical production or loss, surface fluxes or deposition, and entrainment between the boundary layer and free troposphere. The advection of ozone appears to be most appreciable at night with stronger winds in the residual layer, and are on the order of 2 to 4 ppb hr-1. The nighttime chemical loss of ozone due to interaction with NO2 can be estimated by simple numerical modeling of observed quantities and reaction rates, and is found to often roughly compensate for the advection, with typical calculated values of -1 to -3 ppb hr-1. The mixing component is more difficult to directly quantify, but attempts are being made to estimate eddy viscosity by solving for this term in the budget equation. Additionally, small-scale features, such as nocturnal elevated mixed layers, localized BRN (bulk Richardson number) minimums, and low level jets are spotted in systematic ways throughout the flight data, and it is speculated that these may have a role in the transfer of ozone from the residual layer to the surface layer. Ultimately, the preliminary data is promising for the eventual goal of linking together the observed boundary layer evolution with ozone production during air pollution episodes.

Attribution of Recovery in Lower-Stratospheric Ozone

NASA Technical Reports Server (NTRS)

Yang, Eun-Su; Cunnold, Derek M.; Salawitch, Ross J.; McCormick, M. Patrick; Russell, James, III; Zawodny, Joseph M.; Oltmans, Samuel; Newchurch, Michael J.

2005-01-01

Multiple satellite and ground-based observations provide consistent evidence that the thickness of Earth's protective ozone layer has stopped declining since 1997, close to the time of peak stratospheric halogen loading. Regression analyses with Effective Equivalent Stratospheric Chlorine (EESC) in conjunction with further analyses using more sophisticated photochemical model calculations constrained by satellite data demonstrate that the cessation of ozone depletion between 18-25 km altitude is consistent with a leveling off of stratospheric abundances of chlorine and bromine, due to the Montreal Protocol and its amendments. However, ozone increases in the lowest part of the stratosphere, from the tropopause to 18 km, account for about half of the improvement in total column ozone during the past 9 years at northern hemisphere mid-latitudes. The increase in ozone for altitudes below 18 km is most likely driven by changes in transport, rather than driven by declining chlorine and bromine. Even with this evidence that the Montreal Protocol and its amendments are having the desired, positive effect on ozone above 18 km, total column ozone is recovering faster than expected due to the apparent transport driven changes at lower altitudes. Accurate prediction of future levels of stratospheric ozone will require comprehensive understanding of the factors that drive temporal changes at various altitudes, and partitioning of the recent transport-driven increases between natural variability and changes in atmospheric structure perhaps related to anthropogenic climate change.

Attribution of Recovery in Lower-stratospheric Ozone

NASA Technical Reports Server (NTRS)

Yang, Eun-Su; Cunnold, Derek M.; Salawitch, Ross J.; McCormick, M. Patrick; Russell, James, III; Zawodny, Joseph M.; Oltmans, Samuel; Newchurch, Michael J.

2006-01-01

Multiple satellite and ground-based observations provide consistent evidence that the thickness of Earth's protective ozone layer has stopped declining since 1997, close to the time of peak stratospheric halogen loading. Regression analyses with Effective Equivalent Stratospheric Chlorine (EESC) in conjunction with further analyses using more sophisticated photochemical model calculations constrained by satellite data demonstrate that the cessation of ozone depletion between 18-25 km altitude is consistent with a leveling off of stratospheric abundances of chlorine and bromine, due to the Montreal Protocol and its amendments. However, ozone increases in the lowest part of the stratosphere, from the tropopause to 18 km, account for about half of the improvement in total column ozone during the past 9 years at northern hemisphere mid-latitudes. The increase in ozone for altitudes below 18 km is most likely driven by changes in transport, rather than driven by declining chlorine and bromine. Even with this evidence that the Montreal Protocol and its amendments are having the desired, positive effect on ozone above 18 km, total column ozone is recovering faster than expected due to the apparent transport driven changes at lower altitudes. Accurate prediction of future levels of stratospheric ozone will require comprehensive understanding of the factors that drive temporal changes at various altitudes, and partitioning of the recent transport-driven increases between natural variability and changes in atmospheric structure perhaps related to anthropogenic climate change.

STS-87 Day 02 Highlights

NASA Technical Reports Server (NTRS)

1997-01-01

On this second day of the STS-87 mission, the flight crew, Cmdr. Kevin R. Kregel, Pilot Steven W. Lindsey, Mission Specialists Winston E. Scott, Kalpana Chawla, and Takao Doi, and Payload Specialist Leonid K. Kadenyuk are seen conducting experiments involving the effect of weightlessness on materials and fluids. They also work with an experiment to study Earth's protective ozone layers.

JPRS Report: Environmental Issues

DTIC Science & Technology

1993-06-16

Apr 93] ...................... 55 ITALY Environmental Monitoring Project for Amazonia Launched [Eduardo Cagnazzi; ITALIA OGGI, 10 May 93...about the importance of protecting the issued. ozone layer will be raised through TV, radio, newspaper and magazine campaigns. The government will also...being investigated . Office: Matters of study by the Planning Subcommittee Reforming the energy supply structure: Expanding (Meetings 3-5) of the

Analysis of Ozone And CO2 Profiles Measured At A Diary Facility

NASA Astrophysics Data System (ADS)

Ogunjemiyo, S. O.; Hasson, A. S.; Ashkan, S.; Steele, J.; Shelton, T.

2015-12-01

Ozone and carbon dioxide are both greenhouse gasses in the planetary boundary layer. Ozone is a harmful secondary pollutant in the troposphere produced mostly during the day when there is a photochemical reaction in which primary pollutant precursors such as nitrous oxide (NOx) or volatile organic compounds (VOC's) mix with sunlight. As with most pollutants in the lower troposphere, both ozone and carbon dioxide vary in spatial and temporal scale depending on sources of pollution, environmental conditions and the boundary layer dynamics. Among the several factors that influence ozone variation, the seasonal changes in meteorological parameters and availability of ozone precursors are crucial because they control ozone formation and decay. Understanding how the difference in emission sources affect vertical transport of ozone and carbon dioxide is considered crucial to the improvement of their regional inventory sources. The purpose of this study is to characterize vertical transport of ozone and carbon at a diary facility. The study was conducted in the summer of 2011 and 2012 at a commercial dairy facility in Central California and involved profile measurements of ozone and CO2 using electrochemical ozonesondes, meteorological sondes and CO2 probe tethered to a 9 cubic meters helium balloon. On each day of the data collection, multiple balloon launches were made over a period representing different stages of the boundary layer development. The results show ozone and CO2 profiles display different characteristics. Regardless of the time of the day, the CO2 concentration decreases with height with a sharp gradient near the surface that is strengthened by a stable atmospheric condition, a feature suggesting the surface as the source. On the other hand, ozone profiles show greater link to the evolution of the lower boundary layer. Ozone profiles display unique features indicating ozone destruction near the surface. This unusual near the surface, observed even in the afternoon when the boundary layer is fully developed, greatly contrast ozone profiles are typical of urban environment

DOE Office of Scientific and Technical Information (OSTI.GOV)

Reiter, R.; Kanter, H. J.; Sladkovic, R.

The balance of the tropospheric ozone is studied with regard to sources and sinks. The influx of stratospheric ozone through stratospheric intrusions and photochemical production under pure air conditions is discussed. The 4-year measuring series (1977-1980) of the ozone concentration measured at 3 different levels are evaluated, the influence of meteorological parameters is examined. The time variation of the ozone layer between 1000 and 3000 m ASL is investigated as a function of different ozone sources. First results show that stratospheric ozone arriving at the troposphere penetrates only in a few rare cases to the ground layer below 1500 mmore » ASL. Most of the time, the variation of ozone concentration in this layer is determined by photochemical processes which are, in turn, controlled by meteorological parameters. The upper boundary of the photochemically active layer is found at about 500 m above ground. Variability of the concentration of stratospheric aerosol and its optical properties after the volcanic eruptions in the year 1980 are discussed on the basis on lidar backscattering measurements.« less

Children's Ideas about the Ozone Layer and Opportunities for Physics Teaching.

ERIC Educational Resources Information Center

Potts, Alison; And Others

1996-01-01

Examines the potential of global environmental issues as starting points for learning science by studying the preconceptions of children aged 12-13 about the nature, functions, and vulnerability of the ozone layer. Results indicate that children are familiar with the location and nature of the ozone layer but less informed about its magnitude and…

75 FR 38182 - Proposed Collection; Comment Request for Regulation Project

Federal Register 2010, 2011, 2012, 2013, 2014

2010-07-01

... Deplete the Ozone Layer and on Products Containing Such Chemicals (Sec. Sec. 52.4682-1(b), 52.4682-2(b....gov . SUPPLEMENTARY INFORMATION: Title: Excise Tax on Chemicals That Deplete the Ozone Layer and on... Revenue Code sections 4681 and 4682 relating to the tax on chemicals that deplete the ozone layer and on...

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.

Study: Ozone Layer's Future Linked Strongly to Changes in Climate

Science.gov Websites

balloon to measure of the vertical profile of the ozone layer. NOAA scientists launch an ozonesonde via balloon to measure of the vertical profile of the ozone layer. NOAA releases ozonesondes at eight sites worldwide, including the Amundsen-Scott South Pole Station. It also uses satellite and ground-based systems

77 FR 48153 - Protection of Stratospheric Ozone: Request for Methyl Bromide Critical Use Exemption Applications...

Federal Register 2010, 2011, 2012, 2013, 2014

2012-08-13

... ENVIRONMENTAL PROTECTION AGENCY [EPA-HQ-OAR-2012-0375, FRL-9715-7] Protection of Stratospheric Ozone: Request for Methyl Bromide Critical Use Exemption Applications for 2015, Deadline Extension... Stratospheric Ozone Information Hotline, 1-800-296-1996; also http://www.epa.gov/ozone/mbr . Technical...

Mixing Heights and Three-Dimensional Ozone Structure Observed by Airborne Lidar During the 2006 Texas Air Quality Study

NASA Astrophysics Data System (ADS)

Hardesty, R. M.; Senff, C. J.; Alvarez, R. J.; Banta, R. M.; Sandberg, S. P.; Weickmann, A. M.; Darby, L. S.

2007-12-01

A new all solid state ozone lidar was deployed on a NOAA Twin Otter to study boundary layer ozone and aerosol, mostly around Houston, during the 2006 Texas Air Quality Study. The new instrument transmits high pulse-rate, low pulse-energy light at 3 wavelengths in the ultraviolet to obtain ozone profiles with 500 m horizontal resolution and 90 m vertical resolution. During the Texas field study, 20 research flights resulted in nearly 70 hours of ozone measurements during the period from August 1 to September 15. Science objectives included characterization of background ozone levels over rural areas near Houston and Dallas and variability and structure of the boundary layer over different surface types, including urban, wooded, and agricultural land surface areas as well as over Galveston Bay and the Gulf of Mexico. A histogram of all boundary layer ozone concentration measurements showed a bimodal distribution with modes at 45 ppb and 70 ppb. The lower mode correlated with southerly flow, when relatively clean air was transported onshore into the Houston area. Segmenting the observations during southerly flow by region, including the Gulf of Mexico, land within about 55 km from the coast, and further inland indicated that background levels increased by about 10 ppb as air was transported onshore. During the latter part of the experiment, as more pollution was imported into the Houston region, background levels rose to nearly 80 ppb in regions N of Houston. Two flights aimed at observing import of ozone into Texas from the east showed that ozone concentrations increased and boundary layer depths deepened upwind of Houston between September 4 and September 8. Background levels rose by more than 10 ppb over this period. In addition to ozone measurements, we also estimated boundary layer height based on maximum gradient in observed backscatter. The technique worked well when the layer topped by the strongest gradient extends down to the surface. Investigation of the correlation between ozone levels and mixing layer heights both within and external to the Houston urban plume showed a variety of relationships, depending on, e.g., wind direction and occurrence of a bay/gulf breeze. On a day-to-day basis, higher ozone levels were weakly correlated with deeper mixing levels - this was likely due to advection of the urban heat island downwind with the high-ozone urban plume.

Impact of synoptic controls and boundary layer processes on ground-level ozone evolution at an urban site

NASA Astrophysics Data System (ADS)

Haman, Christine Lanier

Houston, Texas frequently exceeds the standard for ground-level ozone during the spring and fall. The large commuting population and vast number of industrial sources provide the necessary ingredients for photochemical ozone production in the presence of favorable meteorological conditions. The lack of continuous boundary layer (BL) observations prevents a comprehensive understanding of its role in ozone evolution. In this study, almost two years of BL observations are utilized to investigate the impacts of synoptic and micrometeorological-scale forcings on ozone. Aerosol gradients derived from ceilometer backscatter retrievals are used to identify the BL and residual layers (RL). Overall agreement is found between ceilometer and sonde estimates of the RL and BL heights (BLH), but difficulty detecting the layers occurs during cloud periods or immediately following precipitation. Large monthly variability is present in the peak afternoon BLH (e.g. mean August and December peaks are ˜2000 and 1100 m, respectively). Monthly nocturnal BLHs display much smaller differences. The majority of ozone exceedances occur during large-scale subsidence and weak winds in a postfrontal environment. These conditions result in turbulent kinetic energy, mechanical mixing, and ventilation processes that are 2--3 times weaker on exceedance days, which inhibit morning BL growth by an average of ˜100 m·hr-1 compared to low ozone days. The spring has higher nocturnal ozone levels, which is likely attributable to longer day lengths (˜78 minutes), stronger winds (˜0.78 m·s -1), and higher background ozone (˜5 ppbv) compared to the fall. Boundary layer entrainment plays an important role in ozone evolution. Exceedance days show a characteristic early morning rapid rise of ozone. Vertical ozone profiles indicate the RL ozone peak is ˜60 ppbv on exceedance days, which is ˜25 ppbv (+/- 10 ppbv) greater than low ozone days. The Integrated Profile Mixing (IPM) and Photochemical Budget (PB) methods are used to quantify ozone transport and photochemical production. On low ozone days, both the IPM and PB methods indicate ozone entrainment is ˜3--4 ppbv·hr-1 in this low photochemical environment of ˜1--4 ppbv·hr-1. During the rapid early morning ozone rise on exceedance days, RL entrainment and photochemical ozone production rates are 5--10 and 10--15 ppbv·hr -1, respectively.

Assessment of Protective Effect of Some Modern Agrochemicals against Ozone-Induced Stress in Sensitive Clover and Tobacco Cultivars.

PubMed

Blum, Oleg; Didyk, Nataliya; Pavluchenko, Nataliya; Godzik, Barbara

2011-01-01

Some modern agrochemicals with antioxidant potential were tested for their protective effect against ozone injury using clover and tobacco ozone-sensitive cultivars as model plants subjected to ambient ozone at two sites (Kyiv city in Ukraine and Szarów village in Poland). All used agrochemicals showed partial protective effects against ozone injury on clover and tobacco. Conducted studies confirmed the effectiveness of modern fungicides belonging to strobilurin group as protectants of sensitive crops against ozone damage. The effectiveness of new growth regulators "Emistym C" and "Agrostymulin" was showed for the first time. Out of the studied agrochemicals, fungicide "Strobi" and natural growth regulator "Emistym C" demonstrated the best protective effects. These agrochemicals present promise for further studies of their possible utilization for enhancement of ozone tolerance of sensitive crops.

Detecting recovery of the stratospheric ozone layer.

PubMed

Chipperfield, Martyn P; Bekki, Slimane; Dhomse, Sandip; Harris, Neil R P; Hassler, Birgit; Hossaini, Ryan; Steinbrecht, Wolfgang; Thiéblemont, Rémi; Weber, Mark

2017-09-13

As a result of the 1987 Montreal Protocol and its amendments, the atmospheric loading of anthropogenic ozone-depleting substances is decreasing. Accordingly, the stratospheric ozone layer is expected to recover. However, short data records and atmospheric variability confound the search for early signs of recovery, and climate change is masking ozone recovery from ozone-depleting substances in some regions and will increasingly affect the extent of recovery. Here we discuss the nature and timescales of ozone recovery, and explore the extent to which it can be currently detected in different atmospheric regions.

Detecting recovery of the stratospheric ozone layer

NASA Astrophysics Data System (ADS)

Chipperfield, Martyn P.; Bekki, Slimane; Dhomse, Sandip; Harris, Neil R. P.; Hassler, Birgit; Hossaini, Ryan; Steinbrecht, Wolfgang; Thiéblemont, Rémi; Weber, Mark

2017-09-01

As a result of the 1987 Montreal Protocol and its amendments, the atmospheric loading of anthropogenic ozone-depleting substances is decreasing. Accordingly, the stratospheric ozone layer is expected to recover. However, short data records and atmospheric variability confound the search for early signs of recovery, and climate change is masking ozone recovery from ozone-depleting substances in some regions and will increasingly affect the extent of recovery. Here we discuss the nature and timescales of ozone recovery, and explore the extent to which it can be currently detected in different atmospheric regions.

Ozone budgets from the Dynamics and Chemistry of Marine Stratocumulus experiment

NASA Technical Reports Server (NTRS)

Kawa, S. R.; Pearson, R., Jr.

1989-01-01

Measurements from the Dynamics and Chemistry of marine Stratocumulus experiment have been used to study components of the regional ozone budget. The surface destruction rate is determined by eddy correlation of ozone and vertical velocity measured by a low-flying aircraft. Significant variability is found in the measured surface resistance; it is partially correlated with friction velocity but appears to have other controlling influences as well. The mean resistance is 4190 s/m which is higher (slower destruction) than most previous estimates for seawater. Flux and mean measurements throughout the marine boundary layer are used to estimate the net rate of in situ photochemical production/destruction of ozone. Averaged over the flights, ozone concentration is found to be near steady state, and a net of photochemical destruction of 0.02-0.07 ng/cu m per sec is diagnosed. This is an important confirmation of photochemical model results for the remote marine boundary layer. Ozone vertical distributions above the boundary layer show a strongly layered structure with very sharp gradients. These distributions are possibly related to the stratospheric ozone source.

Five-year lidar observational results and effects of El Chichon particles on Umkehr ozone data

NASA Astrophysics Data System (ADS)

Uchino, Osamu; Tabata, Isao; Kai, Kenji; Akita, Iwao

1988-08-01

Based on the values of integrated backscattering coefficient B, obtained from the ruby lidar measurements at the Meteorological Research Institude (MRI, at Tsukuba, Japan), the effect of dust particles due to two volcanic eruptions of Mt. El Chichon in 1982 on the Umkehr ozone data at the Tateno Aerological Observatory was determined. In addition, the effects of the aerosols on the Umkehr ozone data at Arosa, Switzerland were investigated using lidar data collected at Garmisch-Partenkirchen, Germany. It was found that both stratospheric and tropospheric aerosols induced a significant negative ozone error in the uppermost layers (33-47 km), caused a small and usually negative ozone error in layers between 16 and 33 km, and induced a significant positive ozone error in layers between 6 and 16 km.

Ozone Transport Aloft Drives Surface Ozone Maxima Across the Mojave Desert

NASA Astrophysics Data System (ADS)

VanCuren, R. A.

2014-12-01

A persistent layer of polluted air in the lower free troposphere over the Mojave Desert (California and Nevada) drives spring and summer surface ozone maxima as deep afternoon mixing delivers ozone and ozone precursors to surface measurement sites 200 km or more downwind of the mountains that separate the deserts from the heavily populated coastal areas of California. Pollutants in this elevated layer derive from California source regions (the Los Angeles megacity region and the intensive agricultural region of the San Joaquin Valley), and from long-range transport from Asia. Recognition of this poorly studied persistent layer explains and expands the significance of previously published reports of ozone and other pollutants observed in and over the Mojave Desert, resolves an apparent paradox in the timing of ozone peaks due to transport from the upwind basins, and provides a new perspective on the long-range downwind impacts of megacity pollution plumes.

Mechanisms of impact of greenhouse gases on the Earth's ozone layer in the Polar Regions

NASA Astrophysics Data System (ADS)

Zadorozhny, Alexander; Dyominov, Igor

A numerical 2-D zonally averaged interactive dynamical radiative-photochemical model of the atmosphere including aerosol physics is used to examine the impact of the greenhouse gases CO2, CH4, and N2O on the future long-term changes of the Earth's ozone layer, in particular on its expected recovery after reduction of anthropogenic discharges of chlorine and bromine compounds into the atmosphere. The model allows calculating self-consistently diabatic circu-lation, temperature, gaseous composition of the troposphere and stratosphere at latitudes from the North to South Poles, as well as distribution of sulphate aerosol particles and polar strato-spheric 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 abun-dance of the greenhouse gases on the long-term changes of the Earth's ozone layer in the Polar Regions, 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 weak-ness 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 be-gins 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 ozone layer here. The difference in the impact of the greenhouse gases on the ozone layer at the southern and northern polar latitudes through PCS modification is determined by the difference in temperature regimes of the Polar Regions. The mechanism of the impact of the greenhouse gases on the polar ozone by means of modification of sulphate aerosol distribution in the atmosphere has been revealed and investigated, too. Numerical experiments show that enhancement of the surface area density of sulphate aerosol in the stratosphere caused by the growth of the greenhouse gases will reduce significantly the ozone depletion during the Antarctic ozone hole.

Characterization of ozone in the lower troposphere during the 2016 G20 conference in Hangzhou.

PubMed

Su, Wenjing; Liu, Cheng; Hu, Qihou; Fan, Guangqiang; Xie, Zhouqing; Huang, Xin; Zhang, Tianshu; Chen, Zhenyi; Dong, Yunsheng; Ji, Xiangguang; Liu, Haoran; Wang, Zhuang; Liu, Jianguo

2017-12-12

Recently, atmospheric ozone pollution has demonstrated an aggravating tendency in China. To date, most research about atmospheric ozone has been confined near the surface, and an understanding of the vertical ozone structure is limited. During the 2016 G20 conference, strict emission control measures were implemented in Hangzhou, a megacity in the Yangtze River Delta, and its surrounding regions. Here, we monitored the vertical profiles of ozone concentration and aerosol extinction coefficients in the lower troposphere using an ozone lidar, in addition to the vertical column densities (VCDs) of ozone and its precursors in the troposphere through satellite-based remote sensing. The ozone concentrations reached a peak near the top of the boundary layer. During the control period, the aerosol extinction coefficients in the lower lidar layer decreased significantly; however, the ozone concentration fluctuated frequently with two pollution episodes and one clean episode. The sensitivity of ozone production was mostly within VOC-limited or transition regimes, but entered a NOx-limited regime due to a substantial decline of NOx during the clean episode. Temporary measures took no immediate effect on ozone pollution in the boundary layer; instead, meteorological conditions like air mass sources and solar radiation intensities dominated the variations in the ozone concentration.

Airborne LIDAR Measurements of Aerosol and Ozone Above the Alberta Oil Sands Region

NASA Astrophysics Data System (ADS)

Aggarwal, M.; Whiteway, J. A.; Seabrook, J.; Gray, L. H.

2014-12-01

Lidar measurements of ozone and aerosol were conducted from a Twin Otter aircraft above the oil sands region of northern Alberta. The field campaign was carried out with a total of five flights out of Fort McMurray, Alberta during the period between August 22 and August 26, 2013. Significant amounts of aerosol were observed within the boundary layer, up to a height of 1.6 km, but the ozone concentration remained at or below background levels. On August 24th the lidar observed a separated layer of aerosol above the boundary layer, at a height of 1.8 km, in which the ozone mixing ratio increased to 70 ppbv. Backward trajectory calculations revealed that the air containing this separated aerosol layer had passed over an area of forest fires. Directly below the layer of forest fire smoke, in the pollution from the oil sands industry, the measured ozone mixing ratio was lower than the background levels (≤35 ppbv).

Retrieval of Surface Ozone from UV-MFRSR Irradiances using Deep Learning

NASA Astrophysics Data System (ADS)

Chen, M.; Sun, Z.; Davis, J.; Zempila, M.; Liu, C.; Gao, W.

2017-12-01

High concentration of surface ozone is harmful to humans and plants. USDA UV-B Monitoring and Research Program (UVMRP) uses Ultraviolet (UV) version of Multi-Filter Rotating Shadowband Radiometer (UV-MFRSR) to measure direct, diffuse, and total irradiances every three minutes at seven UV channels (i.e. 300, 305, 311, 317, 325, 332, and 368 nm channels with 2 nm full width at half maximum). Based on the wavelength dependency of aerosol optical depths, there have been plenty of literatures exploring retrieval methods of total column ozone from UV-MFRSR measurements. However, few has explored the retrieval of surface ozone. The total column ozone is the integral of the multiplication of ozone concentration (varying by height and time) and cross section (varying by wavelength and temperature) over height. Because of the distinctive values of ozone cross section in the UV region, the irradiances at seven UV channels have the potential to resolve the ozone concentration at multiple vertical layers. If the UV irradiances at multiple time points are considered together, the uncertainty or the vertical resolution of ozone concentrations can be further improved. In this study, the surface ozone amounts at the UVMRP station located at Billings, Oklahoma are estimated from the adjacent (i.e. within 200 miles) US Environmental Protection Agency (EPA) surface ozone observations using the spatial analysis technique. Then, the (direct normal) irradiances of UVMRP at one or more time points as inputs and the corresponding estimated surface ozone from EPA as outputs are fed into a pre-trained (dense) deep neural network (DNN) to explore the hidden non-linear relationship between them. This process could improve our understanding of their physical/mathematical relationship. Finally, the optimized DNN is tested with the preserved 5% of the dataset, which are not used during training, to verify the relationship.

SAGE-III Ready for Ozone Checkup

NASA Image and Video Library

2017-02-15

A third-generation investigation into the state of the ozone layer of Earth’s atmosphere is scheduled for launch to the International Space Station on the SpaceX-10 cargo ship. Marilee Roell of NASA’s Langley Research Center explains how the third iteration of the Stratospheric Aerosol and Gas Experiment will measure ozone, aerosols and other components of the atmosphere for scientists who hope to see an improvement in the atmosphere’s ability to protect the planet—and everyone and everything on it—from harmful ultraviolet radiation. For more on ISS science, visit us online: https://www.nasa.gov/mission_pages/station/research/index.html www.twitter.com/iss_research HD download link: https://archive.org/details/TheSpaceProgram _______________________________________ FOLLOW THE SPACE STATION! Twitter: https://twitter.com/Space_Station Facebook: https://www.facebook.com/ISS Instagram: https://instagram.com/iss/ YouTube: https://youtu.be/HQdMZ5OAU3U

Vertical distribution of ozone and VOCs in the low boundary layer of Mexico City

NASA Astrophysics Data System (ADS)

Velasco, E.; Márquez, C.; Bueno, E.; Bernabé, R. M.; Sánchez, A.; Fentanes, O.; Wöhrnschimmel, H.; Cárdenas, B.; Kamilla, A.; Wakamatsu, S.; Molina, L. T.

2007-08-01

The evolution of ozone and 13 volatile organic compounds (VOCs) in the boundary layer of Mexico City was investigated during 2000-2004 to improve our understanding of the complex interactions between those trace gases and meteorological variables, and their influence on the air quality of a polluted megacity. A tethered balloon, fitted with electrochemical and meteorological sondes, was used to obtain detailed vertical profiles of ozone and meteorological parameters up to 1000 m above ground during part of the diurnal cycle (02:00-18:00 h). VOCs samples were collected up to 200 m by pumping air to canisters with a Teflon tube attached to the tether line. Overall, features of these profiles were found to be consistent with a simple picture of nighttime trapping of ozone in an upper residual layer and of VOCs in a shallow unstable layer above the ground. After sunrise an ozone balance is determined by photochemical production, entrainment from the upper residual layer and destruction by titration with NO, delaying the ground-level ozone rise by 2 h. The subsequent evolution of the conductive boundary layer and vertical distribution of pollutants are discussed in terms of the energy balance, the presence of turbulence and the atmospheric stability.

Artificial neural network with backpropagation learning to predict mean monthly total ozone in Arosa, Switzerland

NASA Astrophysics Data System (ADS)

Chattopadhyay, Surajit; Bandyopadhyay, Goutami

2007-01-01

Present study deals with the mean monthly total ozone time series over Arosa, Switzerland. The study period is 1932-1971. First of all, the total ozone time series has been identified as a complex system and then Artificial Neural Networks models in the form of Multilayer Perceptron with back propagation learning have been developed. The models are Single-hidden-layer and Two-hidden-layer Perceptrons with sigmoid activation function. After sequential learning with learning rate 0.9 the peak total ozone period (February-May) concentrations of mean monthly total ozone have been predicted by the two neural net models. After training and validation, both of the models are found skillful. But, Two-hidden-layer Perceptron is found to be more adroit in predicting the mean monthly total ozone concentrations over the aforesaid period.

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.

Emergence of healing in the Antarctic ozone layer

NASA Astrophysics Data System (ADS)

Solomon, Susan; Ivy, Diane J.; Kinnison, Doug; Mills, Michael J.; Neely, Ryan R.; Schmidt, Anja

2016-07-01

Industrial chlorofluorocarbons that cause ozone depletion have been phased out under the Montreal Protocol. A chemically driven increase in polar ozone (or “healing”) is expected in response to this historic agreement. Observations and model calculations together indicate that healing of the Antarctic ozone layer has now begun to occur during the month of September. Fingerprints of September healing since 2000 include (i) increases in ozone column amounts, (ii) changes in the vertical profile of ozone concentration, and (iii) decreases in the areal extent of the ozone hole. Along with chemistry, dynamical and temperature changes have contributed to the healing but could represent feedbacks to chemistry. Volcanic eruptions have episodically interfered with healing, particularly during 2015, when a record October ozone hole occurred after the Calbuco eruption.

Observations of ozone-poor air in the tropical tropopause layer

NASA Astrophysics Data System (ADS)

Newton, Richard; Vaughan, Geraint; Hintsa, Eric; Filus, Michal T.; Pan, Laura L.; Honomichl, Shawn; Atlas, Elliot; Andrews, Stephen J.; Carpenter, Lucy J.

2018-04-01

Ozonesondes reaching the tropical tropopause layer (TTL) over the west Pacific have occasionally measured layers of very low ozone concentrations - less than 15 ppbv - raising the question of how prevalent such layers are and how they are formed. In this paper, we examine aircraft measurements from the Airborne Tropical Tropopause Experiment (ATTREX), the Coordinated Airborne Studies in the Tropics (CAST) and the Convective Transport of Active Species in the Tropics (CONTRAST) experiment campaigns based in Guam in January-March 2014 for evidence of very low ozone concentrations and their relation to deep convection. The study builds on results from the ozonesonde campaign conducted from Manus Island, Papua New Guinea, as part of CAST, where ozone concentrations as low as 12 ppbv were observed between 100 and 150 hPa downwind of a deep convective complex. TTL measurements from the Global Hawk unmanned aircraft show a marked contrast between the hemispheres, with mean ozone concentrations in profiles in the Southern Hemisphere between 100 and 150 hPa of between 10.7 and 15.2 ppbv. By contrast, the mean ozone concentrations in profiles in the Northern Hemisphere were always above 15.4 ppbv and normally above 20 ppbv at these altitudes. The CAST and CONTRAST aircraft sampled the atmosphere between the surface and 120 hPa, finding very low ozone concentrations only between the surface and 700 hPa; mixing ratios as low as 7 ppbv were regularly measured in the boundary layer, whereas in the free troposphere above 200 hPa concentrations were generally well in excess of 15 ppbv. These results are consistent with uplift of almost-unmixed boundary-layer air to the TTL in deep convection. An interhemispheric difference was found in the TTL ozone concentrations, with values < 15 ppbv measured extensively in the Southern Hemisphere but seldom in the Northern Hemisphere. This is consistent with a similar contrast in the low-level ozone between the two hemispheres found by previous measurement campaigns. Further evidence of a boundary-layer origin for the uplifted air is provided by the anticorrelation between ozone and halogenated hydrocarbons of marine origin observed by the three aircraft.

Sun Savvy Students: Free Teaching Resources from EPA's SunWise Program

ERIC Educational Resources Information Center

Hall-Jordan, Luke

2008-01-01

With summer in full swing and the sun is naturally on our minds, what better time to take advantage of a host of free materials provided by the U.S. Environmental Protection Agency's Sun Wise program. Sun Wise aims to teach students and teachers about the stratospheric ozone layer, ultraviolet (UV) radiation, and how to be safe while in the Sun.…

The Importance of the Montreal Protocol in Protecting the Earth's Hydroclimate

NASA Astrophysics Data System (ADS)

Seager, R.; Wu, Y.; Polvani, L. M.

2012-12-01

The 1987 Montreal Protocol regulating emissions of ozone depleting chlorofluorocarbons (CFCs) was motivated primarily by the harm to human health and ecosystems arising from increased exposure to ultraviolet-B (UV-B) radiation associated with depletion from the ozone layer. It is now known that the Montreal Protocol has reduced global warming since CFCs are greenhouse gases (GHGs). In this paper we show that the Montreal Protocol also significantly protects the Earth's hydroclimate, even though this was also not a motivating factor in the decision-making that led to the Protocol. General Circulation Model (GCM) results show that in the coming decade (2020-29), under the 'World Avoided' scenario of no regulations on CFC emissions, the subtropical dry zones would in general get drier, and the middle and high latitude regions wetter. This change is similar, in both pattern and magnitude, to that in the coming decade caused by projected increases in carbon dioxide concentrations. This implies that because of the Montreal Protocol, and the ozone depletion and global warming associated with CFCs thus avoided, the hydrological cycle changes in the coming decade will be significantly less than what they otherwise would have been.

RESULTS OF RESEARCH RELATED TO STRATOSPHERIC OZONE PROTECTION

EPA Science Inventory

Research on ozone protection has been coordinated under the Biological and Climatic Effects Research (BACER) Program. This is a multiagency, multidisciplinary effort initially funded by The Environmental Protection Agency. Its purpose is to reduce uncertainties regarding ozone de...

Cumulus cloud venting of mixed layer ozone

NASA Technical Reports Server (NTRS)

Ching, J. K. S.; Shipley, S. T.; Browell, E. V.; Brewer, D. A.

1985-01-01

Observations are presented which substantiate the hypothesis that significant vertical exchange of ozone and aerosols occurs between the mixed layer and the free troposphere during cumulus cloud convective activity. The experiments utilized the airborne Ultra-Violet Differential Absorption Lidar (UV-DIAL) system. This system provides simultaneous range resolved ozone concentration and aerosol backscatter profiles with high spatial resolution. Evening transects were obtained in the downwind area where the air mass had been advected. Space-height analyses for the evening flight show the cloud debris as patterns of ozone typically in excess of the ambient free tropospheric background. This ozone excess was approximately the value of the concentration difference between the mixed layer and free troposphere determined from independent vertical soundings made by another aircraft in the afternoon.

A multivariate auto-regressive combined-harmonics analysis and its application to ozone time series data

NASA Astrophysics Data System (ADS)

Yang, Eun-Su

2001-07-01

A new statistical approach is used to analyze Dobson Umkehr layer-ozone measurements at Arosa for 1979-1996 and Total Ozone Mapping Spectrometer (TOMS) Version 7 zonal mean ozone for 1979-1993, accounting for stratospheric aerosol optical depth (SAOD), quasi-biennial oscillation (QBO), and solar flux effects. A stepwise regression scheme selects statistically significant periodicities caused by season, SAOD, QBO, and solar variations and filters them out. Auto-regressive (AR) terms are included in ozone residuals and time lags are assumed for the residuals of exogenous variables. Then, the magnitudes of responses of ozone to the SAOD, QBO, and solar index (SI) series are derived from the stationary time series of the residuals. These Multivariate Auto-Regressive Combined Harmonics (MARCH) processes possess the following significant advantages: (1)the ozone trends are estimated more precisely than the previous methods; (2)the influences of the exogenous SAOD, QBO, and solar variations are clearly separated at various time lags; (3)the collinearity of the exogenous variables in the regression is significantly reduced; and (4)the probability of obtaining misleading correlations between ozone and exogenous times series is reduced. The MARCH results indicate that the Umkehr ozone response to SAOD (not a real ozone response but rather an optical interference effect), QBO, and solar effects is driven by combined dynamical radiative-chemical processes. These results are independently confirmed using the revised Standard models that include aerosol and solar forcing mechanisms with all possible time lags but not by the Standard model when restricted to a zero time lag in aerosol and solar ozone forcings. As for Dobson Umkehr ozone measurements at Arosa, the aerosol effects are most significant in layers 8, 7, and 6 with no time lag, as is to be expected due to the optical contamination of Umkehr measurements by SAOD. The QBO and solar UV effects appear in all layers 4-8, and in total ozone. In order to account for annual modulation of the equatorial winds that affects ozone at midlatitudes, a new QBO proxy is selected and applied to the Dobson Umkehr measurements at Arosa. The QBO proxy turns out to be more effective to filter the modulated ozone signals at midlatitudes than the mostly used QBO proxy, the Singapore winds at 30 mb. A statistically significant negative phase relationship is found between solar UV variation and ozone response, especially in layer 4, implying dynamical effects of solar variations on ozone at midlatitudes. Linear negative trends in ozone of -7.8 +/- 1.1 and -5.2 +/- 1.4 [%/decade +/- 2σ] are calculated in layers 7 (~35 km) and 8 (~40 km), respectively, for the period of 1979-1996, with smaller trends of -2.2 +/- 1.0, 1.8 +/- 0.9, and -1.4 +/- 1.1 in layers 6 (~30 km), 5 (~25 km), and 4 (~20 km), respectively. A trend in total ozone (layers 1 through 10) of -2.9 +/- 1.2 [%/decade +/- 2σ] is found over this same period. The aerosol effects obtained from the TOMS zonal means become significant at midlatitudes. QBO ozone contributes to the TOMS zonal means by +/-2 to 4% of their means. The negative solar ozone responses are also found at midlatitudes from the TOMS measurements. The most negative trends from TOMS zonal means are about -6.3 +/- 0.6%/decade at 40-50°N.

40 CFR 97.388 - CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units. 97.388 Section 97.388 Protection of Environment... NOX AND SO2 TRADING PROGRAMS CAIR NOX Ozone Season Opt-in Units § 97.388 CAIR NOX Ozone Season...

40 CFR 97.388 - CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units. 97.388 Section 97.388 Protection of Environment... NOX AND SO2 TRADING PROGRAMS CAIR NOX Ozone Season Opt-in Units § 97.388 CAIR NOX Ozone Season...

40 CFR 97.388 - CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units. 97.388 Section 97.388 Protection of Environment... NOX AND SO2 TRADING PROGRAMS CAIR NOX Ozone Season Opt-in Units § 97.388 CAIR NOX Ozone Season...

40 CFR 97.388 - CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units. 97.388 Section 97.388 Protection of Environment... NOX AND SO2 TRADING PROGRAMS CAIR NOX Ozone Season Opt-in Units § 97.388 CAIR NOX Ozone Season...

40 CFR 97.388 - CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units. 97.388 Section 97.388 Protection of Environment... NOX AND SO2 TRADING PROGRAMS CAIR NOX Ozone Season Opt-in Units § 97.388 CAIR NOX Ozone Season...

40 CFR 52.975 - Redesignations and maintenance plans; ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

...; ozone. 52.975 Section 52.975 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... and maintenance plans; ozone. (a) Approval. The Louisiana Department of Environmental Quality (LDEQ... supplemental ozone redesignation requests and revised maintenance plans. These supplemental submittals were...

40 CFR 52.975 - Redesignations and maintenance plans; ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

...; ozone. 52.975 Section 52.975 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... and maintenance plans; ozone. (a) Approval. The Louisiana Department of Environmental Quality (LDEQ... supplemental ozone redesignation requests and revised maintenance plans. These supplemental submittals were...

40 CFR 52.975 - Redesignations and maintenance plans; ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

...; ozone. 52.975 Section 52.975 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... and maintenance plans; ozone. (a) Approval. The Louisiana Department of Environmental Quality (LDEQ... supplemental ozone redesignation requests and revised maintenance plans. These supplemental submittals were...

40 CFR 52.975 - Redesignations and maintenance plans; ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

...; ozone. 52.975 Section 52.975 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... and maintenance plans; ozone. (a) Approval. The Louisiana Department of Environmental Quality (LDEQ... supplemental ozone redesignation requests and revised maintenance plans. These supplemental submittals were...

Urban and Rural Ozone Pollution Over Lusaka (Zambia, 15.5S, 25E) During SAFARI-2000 (September 2000)

NASA Technical Reports Server (NTRS)

Thompson, Anne M.; Herman, J. R.; Witte, J. C.; Phahlane, A.; Coetzee, G. J. R.; Mukula, C.; Hudson, R. D.; Frolov, A. D.; Bhartia, P. K. (Technical Monitor)

2001-01-01

In early September, throughout south central Africa, seasonal clearing of dry vegetation and the production of charcoal for cooking leads to intense smoke haze and ozone formation. Ozone soundings made over Lusaka during a six-day period in early September 2000 recorded layers of high ozone (greater than 125 ppbv at 5 km) during two stagnant periods, interspersed by a frontal passage that reduced boundary layer ozone by 30 percent. Smoke aerosol column variations aloft and total ozone were monitored by a sun photometer. During the 6-day measurement period, surface ozone concentrations ranged from 50-95 ppbv and integrated tropospheric ozone from the soundings was 39- 54 Dobson Units (note 1.3 km elevation at the launch site). High ozone concentrations above the mixed and inversion layers were advected from rural burning regions in western Zambia where SAFARI aircraft and ground-based instruments observed intense biomass fires and elevated aerosol and trace gas amounts. TOMS tropospheric ozone and smoke aerosols products show the distribution of biomass burning and associated pollution throughout southern Africa in September 2000. Animations of satellite images and trajectories confirm pollutant recirculation over south central African fires, exit of ozone from Mozambique and Tanzania to the Indian Ocean and the characteristic buildup of tropospheric ozone over the Atlantic from western African outflow.

Screening agrochemicals as potential protectants of plants against ozone phytotoxicity.

PubMed

Saitanis, Costas J; Lekkas, Dimitrios V; Agathokleous, Evgenios; Flouri, Fotini

2015-02-01

We tested seven contemporary agrochemicals as potential plant protectants against ozone phytotoxicity. In nine experiments, Bel-W3 tobacco plants were experienced weekly exposures to a) 80 nmol mol(-1) of ozone-enriched or ozone-free air in controlled environment chambers, b) an urban air polluted area, and c) an agricultural-remote area. Ozone caused severe leaf injury, reduced chlorophylls' and total carotenoids' content, and negatively affected photosynthesis and stomatal conductance. Penconazole, (35% ± 8) hexaconazole (28% ± 5) and kresoxim-methyl (28% ± 15) showed higher plants' protection (expressed as percentage; mean ± s.e.) against ozone, although the latter exhibited a high variability. Azoxystrobin (21% ± 15) showed lower protection efficacy and Benomyl (15% ± 9) even lower. Trifloxystrobin (7% ± 11) did not protect the plants at all. Acibenzolar-S-methyl + metalaxyl-M (Bion MX) (-6% ± 17) exhibited the higher variability and contrasting results: in some experiments it showed some protection while in others it intensified the ozone injury by causing phytotoxic symptoms on leaves, even in control plants. Copyright © 2014 Elsevier Ltd. All rights reserved.

[Observation of ozone dry deposition in the field of winter wheat.

PubMed

Li, Shuo; Zheng, You Fei; Wu, Rong Jun; Yin, Ji Fu; Xu, Jing Xin; Zhao, Hui; Sun, Jian

2016-06-01

Ozone is one of the main atmospheric pollutants over surface layer, and its increasing surface ozone concentration and its impact on main crops have become the focus of the public. In order to explore ozone deposition law and environmental factors influencing ozone deposition process, this study used the micrometeorological methods and carried out the experiment under natural conditions. The results showed that during the observational period (the vigorously growing season of wheat), the mean value of ozone flux was -0.35 μg·m -2 ·s -1 (the negative sign indicated that the deposition direction was toward the ground). The mean rate of ozone deposition was 0.55 cm·s -1 . The mean value of aerodynamic resistance was 30 s·m -1 , the mean value of sub-layer resistance was 257 s·m -1 , and that of the canopy layer stomatic resistance was 163 s·m -1 . All the test parameters presented distinct diurnal fluctuation. The ozone deposition resistance was influenced by friction velocity, solar radiation velocity, temperature, relative humidity and other factors.

Stratospheric Ozone Intrusion over the Gulf of Mexico

NASA Astrophysics Data System (ADS)

Pour Biazar, A.; Khan, M. N.; kuang, S.; Park, Y. H.; Emmons, L. K.; McNider, R. T.; Newchurch, M.

2011-12-01

On November 6, 2010, ozonesonde measurements at Huntsville, Alabama, indicated a strong stable and extremely dry layer of air with high ozone concentration right above the boundary layer from 2-km to 3-km altitude. This layer had all the characteristics of stratospheric air. Subsequent investigation using model simulation, satellite observations, and lidar measurements at the site was able to explain this event and indicated that the high ozone was indeed of stratospheric origin and the stratospheric ozone intrusion was due to a tropopause folding event. Model results were compared to lidar measurements of November 5th and 6th and exhibited good agreement suggesting that the model was able to reasonably capture the event. Further examination of the model results shows the extent of the stratospheric incursion over the eastern United States and indicates that the high ozone observed at Huntsville is only a small fragment of the high ozone that was transported over the Gulf of Mexico. The results from this case study show that periodic ozone transport events due to tropopause folding can significantly contribute to the mid-latitude ozone burden in the lower troposphere.

Atmospheric conditions and transport patterns associated with high and low summer ozone levels in the lower troposphere and the boundary layer over the eastern Mediterranean

NASA Astrophysics Data System (ADS)

Kalabokas, Pavlos; Cammas, Jean-Pierre; Thouret, Valerie; Volz-Thomas, Andreas; Boulanger, Damien; Repapis, Christos

2016-04-01

Vertical summertime ozone profiles measured in the period 1994-2008 in the framework of the MOZAIC project over the Eastern Mediterranean basin (especially over the Cairo and Tel-Aviv airports) were analysed, focusing at first in the lower troposphere (1.5-5 km). The vertical profiles collected during extreme days with very high or very low tropospheric ozone mixing ratios have been examined together with the average profiles of relative humidity, carbon monoxide, temperature gradient, wind speed and the corresponding composite maps of geopotential heights at 850 hPa. As a next step, average profiles corresponding, respectively, to the highest and the lowest ozone mixing ratios for the 0-1.5km layer over Cairo in summer are examined along with their corresponding composite maps of geopotential height (and anomalies), vertical velocity (and anomalies), specific humidity anomalies, precipitable water anomalies, air temperature anomalies and wind speed at 850 hPa as well as the corresponding backward trajectories. Based on the above analysis, it turns out that the lower-tropospheric ozone variability over the eastern Mediterranean area is controlled mainly by the synoptic meteorological conditions, combined with local topographical and meteorological features. In particular, the highest ozone concentrations in the lower troposphere and subsequently in the boundary layer are associated with large-scale subsidence of ozone-rich air masses from the upper troposphere under anticyclonic conditions while the lowest ozone concentrations are associated with low pressure conditions inducing uplifting of boundary-layer air, poor in ozone and rich in relative humidity, to the lower troposphere. Also, during the 7% highest ozone days at the 0-1.5km layer over Cairo, very high ozone concentrations of about 80 ppb on average are observed from the surface up to 4-5 km altitude. During the highest ozone days over both airports for the 1.5-5km layer and over Cairo over the 0-1.5km layer, there are extended regions of strong subsidence in the eastern Mediterranean but also in eastern and northern Europe and over these regions the atmosphere is dryer than average. The results of this study will be used within the framework of the MACC project. References Kalabokas, P. D., Cammas, J.-P., Thouret, V., Volz-Thomas, A., Boulanger, D. and Repapis C.C. 2013. Examination of the atmospheric conditions associated with high and low summer ozone levels in the lower troposphere over the eastern Mediterranean. Atmos. Chem. Phys. 13, 10339-10352. DOI: http://dx.doi.org/10.5194/acp-13-10339-2013 Kalabokas P. D., Thouret V., Cammas J.-P., Volz-thomas A., Boulanger D., Repapis C.C., 2015. The geographical distribution of meteorological parameters associated with high and low summer ozone levels in the lower troposphere and the boundary layer over the eastern Mediterranean (Cairo case), Tellus B, 67, 27853, http://dx.doi.org/10.3402/tellusb.v67.27853.

Oceanic protection of prebiotic organic compounds from UV radiation

NASA Technical Reports Server (NTRS)

Cleaves, H. J.; Miller, S. L.; Bada, J. L. (Principal Investigator)

1998-01-01

It is frequently stated that UV light would cause massive destruction of prebiotic organic compounds because of the absence of an ozone layer. The elevated UV flux of the early sun compounds this problem. This applies to organic compounds of both terrestrial and extraterrestrial origin. Attempts to deal with this problem generally involve atmospheric absorbers. We show here that prebiotic organic polymers as well as several inorganic compounds are sufficient to protect oceanic organic molecules from UV degradation. This aqueous protection is in addition to any atmospheric UV absorbers and should be a ubiquitous planetary phenomenon serving to increase the size of planetary habitable zones.

Modeling of Particulate Emissions

DTIC Science & Technology

2011-12-01

Concern Local Air Quality - A Continuing Concern Ground Level Troposphere Ozone Layer Depletion • H2O Ozone Depletion (ice formation) 5 Modeling... Ozone & Smog Formation Health Effects Local Air Quality 33,000-58,000 ft• NOx •Traffic Growth • CO2* • NOx O3* • NOx Reduces CH4 • H2O Vapor...Particulates • SOx Cloud Formation Global Warming * - Greenhouse Gases Ozone Layer Depletion - Not an Immediate Concern Global Warming - An Emerging

Evaluation of the Effect of Exhausts from Liquid and Solid Rockets on Ozone Layer

NASA Astrophysics Data System (ADS)

Yamagiwa, Yoshiki; Ishimaki, Tetsuya

This paper reports the analytical results of the influences of solid rocket and liquid rocket exhausts on ozone layer. It is worried about that the exhausts from solid propellant rockets cause the ozone depletion in the ozone layer. Some researchers try to develop the analytical model of ozone depletion by rocket exhausts to understand its physical phenomena and to find the effective design of rocket to minimize its effect. However, these models do not include the exhausts from liquid rocket although there are many cases to use solid rocket boosters with a liquid rocket at the same time in practical situations. We constructed combined analytical model include the solid rocket exhausts and liquid rocket exhausts to analyze their effects. From the analytical results, we find that the exhausts from liquid rocket suppress the ozone depletion by solid rocket exhausts.

Discharge cell for ozone generator

DOEpatents

Nakatsuka, Suguru

2000-01-01

A discharge cell for use in an ozone generator is provided which can suppress a time-related reduction in ozone concentration without adding a catalytic gas such as nitrogen gas to oxygen gas as a raw material gas. The discharge cell includes a pair of electrodes disposed in an opposed spaced relation with a discharge space therebetween, and a dielectric layer of a three-layer structure consisting of three ceramic dielectric layers successively stacked on at least one of the electrodes, wherein a first dielectric layer of the dielectric layer contacting the one electrode contains no titanium dioxide, wherein a second dielectric layer of the dielectric layer exposed to the discharge space contains titanium dioxide in a metal element ratio of not lower than 10 wt %.

SSTs, nitrogen fertiliser and stratospheric ozone

NASA Technical Reports Server (NTRS)

Turco, R. P.; Whitten, R. C.; Poppoff, I. G.; Capone, L. A.

1978-01-01

A recently revised model of the stratosphere is used to show that a substantial enhancement in the ozone layer could accompany worldwide SST fleet operations and that water vapor may be an important factor in SST assessments. Revised rate coefficients for various ozone-destroying reactions are employed in calculations which indicate a slight increase in the total content of stratospheric ozone for modest-sized fleets of SSTs flying below about 25 km. It is found that water-vapor chemical reactions can negate in large part the NOx-induced ozone gains computed below 25 km and that increased use of nitrogen fertilizer might also enhance the ozone layer.

16 CFR 260.11 - Ozone-safe and ozone-friendly claims.

Code of Federal Regulations, 2013 CFR

2013-01-01

... 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 is... friendly to, the ozone layer or the atmosphere. Example 1: A product is labeled “ozone-friendly.” The claim...

16 CFR 260.11 - Ozone-safe and ozone-friendly claims.

Code of Federal Regulations, 2014 CFR

2014-01-01

... 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 is... friendly to, the ozone layer or the atmosphere. Example 1: A product is labeled “ozone-friendly.” The claim...

A revised global ozone dry deposition estimate based on a new two-layer parameterisation for air-sea exchange and the multi-year MACC composition reanalysis

NASA Astrophysics Data System (ADS)

Luhar, Ashok K.; Woodhouse, Matthew T.; Galbally, Ian E.

2018-03-01

Dry deposition at the Earth's surface is an important sink of atmospheric ozone. Currently, dry deposition of ozone to the ocean surface in atmospheric chemistry models has the largest uncertainty compared to deposition to other surface types, with implications for global tropospheric ozone budget and associated radiative forcing. Most global models assume that the dominant term of surface resistance in the parameterisation of ozone dry deposition velocity at the oceanic surface is constant. There have been recent mechanistic parameterisations for air-sea exchange that account for the simultaneous waterside processes of ozone solubility, molecular diffusion, turbulent transfer, and first-order chemical reaction of ozone with dissolved iodide and other compounds, but there are questions about their performance and consistency. We present a new two-layer parameterisation scheme for the oceanic surface resistance by making the following realistic assumptions: (a) the thickness of the top water layer is of the order of a reaction-diffusion length scale (a few micrometres) within which ozone loss is dominated by chemical reaction and the influence of waterside turbulent transfer is negligible; (b) in the water layer below, both chemical reaction and waterside turbulent transfer act together and are accounted for; and (c) chemical reactivity is present through the depth of the oceanic mixing layer. The new parameterisation has been evaluated against dry deposition velocities from recent open-ocean measurements. It is found that the inclusion of only the aqueous iodide-ozone reaction satisfactorily describes the measurements. In order to better quantify the global dry deposition loss and its interannual variability, modelled 3-hourly ozone deposition velocities are combined with the 3-hourly MACC (Monitoring Atmospheric Composition and Climate) reanalysis ozone for the years 2003-2012. The resulting ozone dry deposition is found to be 98.4 ± 30.0 Tg O3 yr-1 for the ocean and 722.8 ± 87.3 Tg O3 yr-1 globally. The new estimate of the ocean component is approximately a third of the current model estimates. This reduction corresponds to an approximately 20 % decrease in the total global ozone dry deposition, which (with all other components being unchanged) is equivalent to an increase of approximately 5 % in the modelled tropospheric ozone burden and a similar increase in tropospheric ozone lifetime.

Tropospheric ozone over the North Pacific from ozonesonde observations

NASA Astrophysics Data System (ADS)

Oltmans, S. J.; Johnson, B. J.; Harris, J. M.; Thompson, A. M.; Liu, H. Y.; Chan, C. Y.; VöMel, H.; Fujimoto, T.; Brackett, V. G.; Chang, W. L.; Chen, J.-P.; Kim, J. H.; Chan, L. Y.; Chang, H.-W.

2004-08-01

As part of the Transport and Chemical Evolution over the Pacific (TRACE-P) mission, ozonesondes were used to make ozone vertical profile measurements at nine locations in the North Pacific. At most of the sites there is a multiyear record of observations. From locations in the western Pacific (Hong Kong; Taipei; Jeju Island, Korea; and Naha, Kagoshima, Tsukuba, and Sapporo, Japan), a site in the central Pacific (Hilo, Hawaii), and a site on the west coast of the United States (Trinidad Head, California) both a seasonal and event specific picture of tropospheric ozone over the North Pacific emerges. Ozone profiles over the North Pacific generally show a prominent spring maximum throughout the troposphere. This maximum is tied to the location of the jet stream and its influence on stratosphere-troposphere exchange and the increase in photochemical ozone production through the spring. Prominent layers of enhanced ozone in the middle and upper troposphere north of about 30°N seem to be more closely tied to stratospheric intrusions while biomass burning leads to layers of enhanced ozone in the lower and upper troposphere at Hong Kong (22°N) and Taipei (25°N). The lower free tropospheric layers at Hong Kong are associated with burning in SE Asia, but the upper layer may be associated with either equatorial Northern Hemisphere burning in Africa or SE Asian biomass burning. In the boundary layer at Taipei very high mixing ratios of ozone were observed that result from pollution transport from China in the spring and local urban pollution during the summer. At the ozonesonde site near Tokyo (Tsukuba, 36°N) very large enhancements of ozone are seen in the boundary layer in the summer that are characteristic of urban air pollution. At sites in the mid and eastern Pacific the signature of transport of polluted air from Asia is not readily identifiable from the ozonesonde profile. This is likely due to the more subtle signal and the fact that from the ozone profile and meteorological data by themselves it is difficult to identify such a signal. During the TRACE-P intensive campaign period (February-April 2001), tropospheric ozone amounts were generally typical of those seen in the long-term records of the stations with multiyear soundings. The exception was the upper troposphere over Hong Kong and Taipei where ozone amounts were lower in 2001.

40 CFR 52.1982 - Control strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Ozone. 52.1982 Section 52.1982 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS...: Ozone. (a) Part D—Approval. (1) The Salem/ Portland and Medford/Ashland area attainment plans are...

40 CFR 52.1982 - Control strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.1982 Section 52.1982 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS...: Ozone. (a) Part D—Approval. (1) The Salem/ Portland and Medford/Ashland area attainment plans are...

40 CFR 52.1982 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.1982 Section 52.1982 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS...: Ozone. (a) Part D—Approval. (1) The Salem/ Portland and Medford/Ashland area attainment plans are...

40 CFR 52.1982 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.1982 Section 52.1982 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS...: Ozone. (a) Part D—Approval. (1) The Salem/ Portland and Medford/Ashland area attainment plans are...

40 CFR 52.1982 - Control strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.1982 Section 52.1982 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS...: Ozone. (a) Part D—Approval. (1) The Salem/ Portland and Medford/Ashland area attainment plans are...

78 FR 20004 - Protection of Stratospheric Ozone: Adjustments to the Allowance System for Controlling HCFC...

Federal Register 2010, 2011, 2012, 2013, 2014

2013-04-03

... Protection of Stratospheric Ozone: Adjustments to the Allowance System for Controlling HCFC Production... adjusting the allowance system controlling U.S. consumption and production of hydrochlorofluorocarbons... ``Protection of Stratospheric Ozone: Adjustments to the Allowance System for Controlling HCFC Production...

77 FR 16988 - Protection of Stratospheric Ozone: Amendment to HFO-1234yf SNAP Rule for Motor Vehicle Air...

Federal Register 2010, 2011, 2012, 2013, 2014

2012-03-23

... Protection of Stratospheric Ozone: Amendment to HFO-1234yf SNAP Rule for Motor Vehicle Air Conditioning... hydrofluoroolefin (HFO)-1234yf (2,3,3,3-tetrafluoroprop-1-ene), a substitute for ozone- depleting substances (ODSs... EPA's Stratospheric Ozone Web site at http://www.epa.gov/ozone/snap/regs . The full list of SNAP...

40 CFR 96.388 - CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units. 96.388 Section 96.388 Protection of Environment... SO2 TRADING PROGRAMS FOR STATE IMPLEMENTATION PLANS CAIR NOX Ozone Season Opt-in Units § 96.388 CAIR...

40 CFR 96.388 - CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units. 96.388 Section 96.388 Protection of Environment... SO2 TRADING PROGRAMS FOR STATE IMPLEMENTATION PLANS CAIR NOX Ozone Season Opt-in Units § 96.388 CAIR...

40 CFR 96.388 - CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units. 96.388 Section 96.388 Protection of Environment... SO 2 TRADING PROGRAMS FOR STATE IMPLEMENTATION PLANS CAIR NOX Ozone Season Opt-in Units § 96.388 CAIR...

40 CFR 96.388 - CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units. 96.388 Section 96.388 Protection of Environment... SO2 TRADING PROGRAMS FOR STATE IMPLEMENTATION PLANS CAIR NOX Ozone Season Opt-in Units § 96.388 CAIR...

40 CFR 96.388 - CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false CAIR NOX Ozone Season allowance allocations to CAIR NOX Ozone Season opt-in units. 96.388 Section 96.388 Protection of Environment... SO2 TRADING PROGRAMS FOR STATE IMPLEMENTATION PLANS CAIR NOX Ozone Season Opt-in Units § 96.388 CAIR...

40 CFR 52.2428 - Control Strategy: Carbon monoxide and ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... ozone. 52.2428 Section 52.2428 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control Strategy: Carbon monoxide and ozone. (a) Determination—EPA has determined that, as of November 5, 1997, the Richmond ozone nonattainment area, which consists of the counties of Chesterfield, Hanover...

40 CFR 52.2428 - Control Strategy: Carbon monoxide and ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... ozone. 52.2428 Section 52.2428 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control Strategy: Carbon monoxide and ozone. (a) Determination—EPA has determined that, as of November 5, 1997, the Richmond ozone nonattainment area, which consists of the counties of Chesterfield, Hanover...

40 CFR 52.2428 - Control Strategy: Carbon monoxide and ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... ozone. 52.2428 Section 52.2428 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control Strategy: Carbon monoxide and ozone. (a) Determination—EPA has determined that, as of November 5, 1997, the Richmond ozone nonattainment area, which consists of the counties of Chesterfield, Hanover...

40 CFR 52.2428 - Control Strategy: Carbon monoxide and ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... ozone. 52.2428 Section 52.2428 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control Strategy: Carbon monoxide and ozone. (a) Determination—EPA has determined that, as of November 5, 1997, the Richmond ozone nonattainment area, which consists of the counties of Chesterfield, Hanover...

40 CFR 52.975 - Redesignations and maintenance plans; ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

...; ozone. 52.975 Section 52.975 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... and maintenance plans; ozone. Link to an amendment published at 78 FR 27062, May 9, 2013. (a) Approval..., however. The LDEQ addressed these approvability issues in supplemental ozone redesignation requests and...

40 CFR 52.2428 - Control Strategy: Carbon monoxide and ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... ozone. 52.2428 Section 52.2428 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... Control Strategy: Carbon monoxide and ozone. (a) Determination—EPA has determined that, as of November 5, 1997, the Richmond ozone nonattainment area, which consists of the counties of Chesterfield, Hanover...

77 FR 74381 - Protection of Stratospheric Ozone: Listing of Substitutes for Ozone Depleting Substances-Fire...

Federal Register 2010, 2011, 2012, 2013, 2014

2012-12-14

... Protection of Stratospheric Ozone: Listing of Substitutes for Ozone Depleting Substances--Fire Suppression... a companion proposed rule issuing listings for three fire suppressants under EPA's Significant New... companion proposed rule issuing listings for three fire suppressants under EPA's Significant New...

Lidar Observations of the Vertical Structure of Ozone and Aerosol during Wintertime High-Ozone Episodes Associated with Oil and Gas Exploration in the Uintah Basin

NASA Astrophysics Data System (ADS)

Senff, C. J.; Langford, A. O.; Banta, R. M.; Alvarez, R. J.; Weickmann, A.; Sandberg, S.; Marchbanks, R. D.; Brewer, A.; Hardesty, R. M.

2013-12-01

The Uintah Basin in northeast Utah has been experiencing extended periods of poor air quality in the winter months including very high levels of surface ozone. To investigate the causes of these wintertime ozone pollution episodes, two comprehensive studies were undertaken in January/February of 2012 and 2013. As part of these Uintah Basin Ozone Studies (UBOS), NOAA deployed its ground-based, scanning Tunable Optical Profiler for Aerosol and oZone (TOPAZ) lidar to document the vertical structure of ozone and aerosol backscatter from near the surface up to about 3 km above ground level (AGL). TOPAZ, along with a comprehensive set of chemistry and meteorological measurements, was situated in both years at the Horse Pool site at the northern edge of a large concentration of gas producing wells in the eastern part of the Uintah Basin. The 2012 study was characterized by unusually warm and snow-free condition and the TOPAZ lidar observed deep boundary layers (BL) and mostly well-mixed vertical ozone profiles at or slightly above tropospheric background levels. During UBOS 2013, winter weather conditions in the Uintah Basin were more typical with snow-covered ground and a persistent, shallow cold-pool layer. The TOPAZ lidar characterized with great temporal and spatial detail the evolution of multiple high-ozone episodes as well as cleanout events caused by the passage of synoptic-scale storm systems. Despite the snow cover, the TOPAZ observations show well-mixed afternoon ozone and aerosol profiles up to about 100 m AGL. After several days of pollutant buildup, BL ozone values reached 120-150 ppbv. Above the mixed layer, ozone values gradually decreased to tropospheric background values of around 50 ppbv throughout the several-hundred-meter-deep cold-pool layer and then stayed constant above that up to about 3 km AGL. During the ozone episodes, the lidar observations show no indication of either vertical or horizontal transport of high ozone levels to the surface, thus supporting the notion that ozone is locally produced in the Uintah Basin. In both winters, TOPAZ occasionally observed ozone titration as the NOx-rich plume from the nearby Bonanza power plant was advected over the Horse Pool site. In 2012, low ozone values due to titration were observed at the surface and throughout the well-mixed BL, while in 2013 low ozone values were confined to the upper part of the cold-pool layer above the BL. This suggests that power plant NOx was very likely not part of the precursor mix that led to the high surface ozone values observed in 2013.

Space Shuttle Project

NASA Image and Video Library

1995-03-18

The Space Shuttle Endeavour (STS-67) lands at Edwards Air Force Base in southern California after successfully completing NASA's longest plarned shuttle mission. The seven-member crew conducted round-the-clock observations with the ASTRO-2 observatory, a trio of telescopes designed to study the universe of ultraviolet astronomy. Because of Earth's protective ozone layer ultraviolet light from celestial objects does not reach gound-based telescopes, and such studies can only be conducted from space.

Addressing Ozone Layer Depletion

EPA Pesticide Factsheets

Access information on EPA's efforts to address ozone layer depletion through regulations, collaborations with stakeholders, international treaties, partnerships with the private sector, and enforcement actions under Title VI of the Clean Air Act.

Ozone: What Would It Be Like to Live in a World Where the Sun Was Dangerous?

ERIC Educational Resources Information Center

Clearing, 1992

1992-01-01

Defines ozone layer and the meaning, evidence, causes, and significance of ozone depletion. Summarizes solutions to the problem of ozone depletion and government action concerning the issue. Graphically depicts ozone depletion, global ozone loss, and how ozone is destroyed. Provides a lesson plan and listing for additional educational resources.…

Upper atmospheric effects of the hf active auroral research program ionospheric research instrument (HAARP IRI)

DOE Office of Scientific and Technical Information (OSTI.GOV)

Eccles, V.; Armstrong, R.

1993-05-01

The earth's ozone layer occurs in the stratosphere, primarily between 10 and 30 miles altitude. The amount of ozone, O3, present is the result of a balance between production and destruction processes. Experiments have shown that natural processes such as auroras create molecules that destroy O. One family of such molecules is called odd nitrogen of which nitric oxide (NO) is an example. Because the HAARP (HF Active Auroral Research Program) facility is designed to mimic and investigate certain natural processes, a study of possible effects of HAARP on the ozone layer was conducted. The study used a detailed modelmore » of the thermal and chemical effects of the high power HF beam, which interacts with free electrons in the upper atmosphere above 50 miles altitude. It was found only a small fraction of the beam energy goes into the production of odd nitrogen molecules, whereas odd nitrogen is efficiently produced by auroras. Since the total energy emitted by HAARP in the year is some 200,000 times less than the energy deposited in the upper atmosphere by auroras, the study demonstrates that HAARP HF beam experiments will cause no measurable depletion of the earth's ozone layer.... Ozone, Ozone depletion, Ozone layer, Odd nitrogen, Nitric oxide, HAARP Emitter characteristics.« less

Seasonal Ozone Variations in the Isentropic Layer between 330 and 380 K as Observed by SAGE 2: Implications of Extratropical Cross-Tropopause Transport

NASA Technical Reports Server (NTRS)

Wang, Pi-Huan; Cunnold, Derek M.; Zawodny, Joseph M.; Pierce, R. Bradley; Olson, Jennifer R.; Kent, Geoffrey S.; Skeens, Kristi, M.

1998-01-01

To provide observational evidence on the extratropical cross-tropopause transport between the stratosphere and the troposphere via quasi-isentropic processes in the middleworld (the part of the atmosphere in which the isentropic surfaces intersect the tropopause), this report presents an analysis of the seasonal variations of the ozone latitudinal distribution in the isentropic layer between 330 K and 380 K based on the measurements from the Stratospheric Aerosol and Gas Experiment (SAGE) II. The results from SAGE II data analysis are consistent with (1) the buildup of ozone-rich air in the extratropical middleworld through the large-scale descending mass circulation during winter, (2) the spread of ozone-rich air in the isentropic layer from midlatitudes to subtropics via quasi-isentropic transport during spring, (3) significant photochemical ozone removal and the absence of an ozone-rich supply of air to the layer during summer, and (4) air mass exchange between the subtropics and the extratropics during the summer monsoon period. Thus the SAGE II observed ozone seasonal variations in the middleworld are consistent with the existing model calculated annual cycle of the diabatic circulation as well as the conceptual role of the eddy quasi-adiabatic transport in the stratosphere-troposphere exchange reported in the literature.

Emergence of healing in the Antarctic ozone layer.

PubMed

Solomon, Susan; Ivy, Diane J; Kinnison, Doug; Mills, Michael J; Neely, Ryan R; Schmidt, Anja

2016-07-15

Industrial chlorofluorocarbons that cause ozone depletion have been phased out under the Montreal Protocol. A chemically driven increase in polar ozone (or "healing") is expected in response to this historic agreement. Observations and model calculations together indicate that healing of the Antarctic ozone layer has now begun to occur during the month of September. Fingerprints of September healing since 2000 include (i) increases in ozone column amounts, (ii) changes in the vertical profile of ozone concentration, and (iii) decreases in the areal extent of the ozone hole. Along with chemistry, dynamical and temperature changes have contributed to the healing but could represent feedbacks to chemistry. Volcanic eruptions have episodically interfered with healing, particularly during 2015, when a record October ozone hole occurred after the Calbuco eruption. Copyright © 2016, American Association for the Advancement of Science.

40 CFR 52.1486 - Control strategy: Hydrocarbons and ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... ozone. 52.1486 Section 52.1486 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... strategy: Hydrocarbons and ozone. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for the attainment and maintenance of the national standard for ozone in the Las...

40 CFR 52.1486 - Control strategy: Hydrocarbons and ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... ozone. 52.1486 Section 52.1486 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... strategy: Hydrocarbons and ozone. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for the attainment and maintenance of the national standard for ozone in the Las...

40 CFR 52.1486 - Control strategy: Hydrocarbons and ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... ozone. 52.1486 Section 52.1486 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... strategy: Hydrocarbons and ozone. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for the attainment and maintenance of the national standard for ozone in the Las...

40 CFR 52.1486 - Control strategy: Hydrocarbons and ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... ozone. 52.1486 Section 52.1486 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... strategy: Hydrocarbons and ozone. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for the attainment and maintenance of the national standard for ozone in the Las...

40 CFR 52.1486 - Control strategy: Hydrocarbons and ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... ozone. 52.1486 Section 52.1486 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR... strategy: Hydrocarbons and ozone. (a) The requirements of subpart G of this chapter are not met since the plan does not provide for the attainment and maintenance of the national standard for ozone in the Las...

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 the...

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 Maintenance...

40 CFR 51.241 - Nonattainment areas for carbon monoxide and ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... Intergovernmental Consultation Agency Designation § 51.241 Nonattainment areas for carbon monoxide and ozone. (a... 40 Protection of Environment 2 2011-07-01 2011-07-01 false Nonattainment areas for carbon monoxide and ozone. 51.241 Section 51.241 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED...

40 CFR 51.241 - Nonattainment areas for carbon monoxide and ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... Intergovernmental Consultation Agency Designation § 51.241 Nonattainment areas for carbon monoxide and ozone. (a... 40 Protection of Environment 2 2014-07-01 2014-07-01 false Nonattainment areas for carbon monoxide and ozone. 51.241 Section 51.241 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED...

40 CFR 51.241 - Nonattainment areas for carbon monoxide and ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... Intergovernmental Consultation Agency Designation § 51.241 Nonattainment areas for carbon monoxide and ozone. (a... 40 Protection of Environment 2 2013-07-01 2013-07-01 false Nonattainment areas for carbon monoxide and ozone. 51.241 Section 51.241 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED...

40 CFR 51.241 - Nonattainment areas for carbon monoxide and ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... Intergovernmental Consultation Agency Designation § 51.241 Nonattainment areas for carbon monoxide and ozone. (a... 40 Protection of Environment 2 2010-07-01 2010-07-01 false Nonattainment areas for carbon monoxide and ozone. 51.241 Section 51.241 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED...

40 CFR 51.241 - Nonattainment areas for carbon monoxide and ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... Intergovernmental Consultation Agency Designation § 51.241 Nonattainment areas for carbon monoxide and ozone. (a... 40 Protection of Environment 2 2012-07-01 2012-07-01 false Nonattainment areas for carbon monoxide and ozone. 51.241 Section 51.241 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED...

Cooperative endeavors: A case study of success

DOE Office of Scientific and Technical Information (OSTI.GOV)

Baker, J.

1997-12-31

Partnerships and cooperative agreements abound in the environmental arena today. This paper briefly highlights the collaborative approach used by the International Cooperative for Ozone Layer Protection (ICOLP). ICOLP has helped international members and non-members to eliminate most of the ozone-depleting solvents from manufacturing processes through the exchange of technical information in a non-proprietary manner. By using alternatives, companies and governments have realized savings in the multiple millions of dollars. Advantages of participating in cooperative environmental partnerships may include: (1) improved access and exchange of information, (2) cost minimization, (3) promotion and facilitation of business opportunities, (4) improved dialogue between groups,more » (5) coordinated approach to complex issues, and (6) technology development and transfer opportunities.« less

Impact of Future Volcanic Eruptions on Stratospheric Ozone

NASA Astrophysics Data System (ADS)

Wilmouth, D. M.; Klobas, J. E.; Weisenstein, D.; Anderson, J. G.; Salawitch, R. J.

2017-12-01

Due to the anthropogenic release of chlorine-containing chemicals such as chlorofluorocarbons into the atmosphere in the twentieth century, a large volcanic eruption occurring today would initiate chemical reactions that reduce the thickness of the ozone layer. In the future, when atmospheric levels of chlorine are reduced, large volcanic eruptions are instead expected to increase the thickness of the ozone layer, but important details relevant to this shift in volcanic impact are not well known. Here we use the AER-2D chemical transport model to simulate a Pinatubo-like volcanic eruption in contemporary and future atmospheres. In particular, we explore the sensitivity of column ozone to volcanic eruption for four different climate change scenarios over the remainder of this century and also establish the importance of bromine-containing very short-lived substances (VSLS) in determining whether future eruptions will lead to ozone depletion. We find that the ozone layer will be vulnerable to volcanic perturbation for considerably longer than previously believed. Finally, we consider the impact on column ozone of inorganic halogens being co-injected into the stratosphere following future explosive eruptions using realistic hydrogen halide to sulfur dioxide ratios.

Understanding Ozone: Exploring the Good and Bad Facets of a Famous Gas.

ERIC Educational Resources Information Center

Hanif, Muhammad

1995-01-01

Presents activities that help students distinguish between the beneficial layer of stratospheric ozone and the dangerous ground-level or tropospheric ozone, understand the chemical processes of ozone breakdown in the stratosphere, find the sources of ground-level ozone, and explore the differences in the patterns of ozone concentration over the…

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 ...

Ozone nighttime recovery in the marine boundary layer: Measurement and simulation of the ozone diurnal cycle at Reunion Island

NASA Astrophysics Data System (ADS)

Bremaud, P. J.; Taupin, F.; Thompson, A. M.; Chaumerliac, N.

1998-02-01

We describe the diurnal cycle of ozone in the marine boundary layer measured at Reunion Island (21°S, 55°E) in the western part of the Indian Ocean in August-September 1995. Results from a box chemistry model are compared with ozone measurements at Reunion Island. We focus on the peak-to-peak amplitude of ozone concentration, since our measurements show a variation of about 4 parts per billion by volume, which is close to the value obtained by Johnson et al. [1990] during the Soviet-American Gases and Aerosols (SAGA) 1987 Indian Ocean cruise. Different dynamical mechanisms are examined in order to reproduce such a variation. We conclude that the most important one is the exchange between the ozone-rich free troposphere and the ozone-poor boundary layer. This exchange is supposed to be more important during the night than during the day, allowing ozone nighttime recovery. This is the key point of the observed diurnal cycle, since daytime ozone photochemistry is well described by the model. Then we assume an entrainment velocity equal to 1 mm s-1 during the day and 14 mm s-1 during the night to closely match our measurements. Topography influences, together with clouds, are presumed to be responsible for this difference between nighttime and daytime entrainment velocities of free tropospheric air into the boundary layer at Reunion Island. Over the open ocean the difference of the turbulent flux of sensible heat between the day and the night explains the strong ozone nighttime recovery observed by us and by Johnson et al. [1990].

The impact on the ozone layer from NOx produced by terrestrial gamma ray flashes

NASA Astrophysics Data System (ADS)

Cramer, E. S.; Briggs, M. S.; Liu, N.; Mailyan, B.; Dwyer, J. R.; Rassoul, H. K.

2017-05-01

The motivation of this work is to understand the effects of terrestrial gamma ray flashes (TGFs) on the ozone layer. One of the main ozone-destroying mechanisms is the production of NOx in the stratospheric region. NOx from lightning has been considered as a possible cause of ozone depletion, but probably little of this NOx is transported from the tropopause to the stratosphere. Since the energetic particles of TGFs travel from ≈12 km to space, the resulting ionization can produce NOx directly in the stratosphere. In order to quantify the production of stratospheric NOx from TGFs, we use the Runaway Electron Avalanche Model to simulate a typical setup of the acceleration region inside a thundercloud. The photons are then transported through the Earth's atmosphere, where they deposit some of their energy as ionization in the ozone layer. We then calculate the number of NOx molecules produced by considering the average energy required to produce one electron-ion pair. Finally, the effect of TGF NOx production is estimated using the global annual rate of TGFs. It is estimated that the NOx production of TGFs is completely negligible compared to other sources, and therefore, TGFs have no effect on the ozone layer.

Chemical processes related to net ozone tendencies in the free troposphere

NASA Astrophysics Data System (ADS)

Bozem, Heiko; Butler, Tim M.; Lawrence, Mark G.; Harder, Hartwig; Martinez, Monica; Kubistin, Dagmar; Lelieveld, Jos; Fischer, Horst

2017-09-01

Ozone (O3) is an important atmospheric oxidant, a greenhouse gas, and a hazard to human health and agriculture. Here we describe airborne in situ measurements and model simulations of O3 and its precursors during tropical and extratropical field campaigns over South America and Europe, respectively. Using the measurements, net ozone formation/destruction tendencies are calculated and compared to 3-D chemistry-transport model simulations. In general, observation-based net ozone tendencies are positive in the continental boundary layer and the upper troposphere at altitudes above ˜ 6 km in both environments. On the other hand, in the marine boundary layer and the middle troposphere, from the top of the boundary layer to about 6-8 km altitude, net O3 destruction prevails. The ozone tendencies are controlled by ambient concentrations of nitrogen oxides (NOx). In regions with net ozone destruction the available NOx is below the threshold value at which production and destruction of O3 balance. While threshold NO values increase with altitude, in the upper troposphere NOx concentrations are generally higher due to the integral effect of convective precursor transport from the boundary layer, downward transport from the stratosphere and NOx produced by lightning. Two case studies indicate that in fresh convective outflow of electrified thunderstorms net ozone production is enhanced by a factor 5-6 compared to the undisturbed upper tropospheric background. The chemistry-transport model MATCH-MPIC generally reproduces the pattern of observation-based net ozone tendencies but mostly underestimates the magnitude of the net tendency (for both net ozone production and destruction).

Causes and effects of a hole. [in Antarctic ozone layer

NASA Technical Reports Server (NTRS)

Margitan, J. J.

1987-01-01

Preliminary results from the U.S. National Ozone Expedition (NOZE) to Antarctica are reviewed. The NOZE ozonesonde measurements showed significant vertical structure in the hole, with 80 percent depletion in some of the 1 km layers but only 20 percent in adjacent layers. The depletion was confined to the 12-20 km region, beginning first at higher altitude and progressing downward. This is strong evidence against the theory that the ozone hole is due to solar activity producing odd nitrogen at high altitudes which is transported downwards, leading to enhanced odd-nitrogen catalytic cycles that destroy ozone. Nitrous oxide data show unusually low concentrations within the polar vortex, which is evidence against the theory that the hole is caused by a purely dynamical mechanism in which rising air motions within the polar vortex lead to reduced column densities of ozone. It is tentatively concluded that a chemical mechanism involving man-made chlorofluorocarbons is the likely cause of ozone depletion in the hole.

40 CFR Appendix F to Subpart A of... - Listing of Ozone-Depleting Chemicals

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 18 2014-07-01 2014-07-01 false Listing of Ozone-Depleting Chemicals F...) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE Production and Consumption Controls Pt. 82, Subpt. A, App. F Appendix F to Subpart A of Part 82—Listing of Ozone-Depleting Chemicals Controlled...

40 CFR Appendix F to Subpart A of... - Listing of Ozone-Depleting Chemicals

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 18 2012-07-01 2012-07-01 false Listing of Ozone-Depleting Chemicals F...) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE Production and Consumption Controls Pt. 82, Subpt. A, App. F Appendix F to Subpart A of Part 82—Listing of Ozone-Depleting Chemicals Controlled...

40 CFR 52.426 - Control strategy plans for attainment and rate-of-progress: ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... and rate-of-progress: ozone. 52.426 Section 52.426 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.426 Control strategy plans for attainment and rate-of-progress: ozone. (a) EPA fully approves, as... Delaware portion of the Philadelphia-Wilmington-Trenton severe ozone nonattainment, namely Kent and New...

40 CFR Appendix F to Subpart A of... - Listing of Ozone-Depleting Chemicals

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 18 2013-07-01 2013-07-01 false Listing of Ozone-Depleting Chemicals F...) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE Production and Consumption Controls Pt. 82, Subpt. A, App. F Appendix F to Subpart A of Part 82—Listing of Ozone-Depleting Chemicals Controlled...

40 CFR 52.426 - Control strategy plans for attainment and rate-of-progress: ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... and rate-of-progress: ozone. 52.426 Section 52.426 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.426 Control strategy plans for attainment and rate-of-progress: ozone. (a) EPA fully approves, as... Delaware portion of the Philadelphia-Wilmington-Trenton severe ozone nonattainment, namely Kent and New...

40 CFR 52.426 - Control strategy plans for attainment and rate-of-progress: ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... and rate-of-progress: ozone. 52.426 Section 52.426 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.426 Control strategy plans for attainment and rate-of-progress: ozone. (a) EPA fully approves, as... Delaware portion of the Philadelphia-Wilmington-Trenton severe ozone nonattainment, namely Kent and New...

40 CFR 52.426 - Control strategy plans for attainment and rate-of-progress: ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... and rate-of-progress: ozone. 52.426 Section 52.426 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.426 Control strategy plans for attainment and rate-of-progress: ozone. (a) EPA fully approves, as... Delaware portion of the Philadelphia-Wilmington-Trenton severe ozone nonattainment, namely Kent and New...

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

... Part II Environmental Protection Agency 40 CFR Parts 50, 58 and 81 Ozone National Ambient Air... 2008 Ozone National Ambient Air Quality Standards AGENCY: Environmental Protection Agency (EPA). ACTION... designations for the ozone national ambient air quality standards (NAAQS) that were promulgated in March 2008...

40 CFR 52.426 - Control strategy plans for attainment and rate-of-progress: ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... and rate-of-progress: ozone. 52.426 Section 52.426 Protection of Environment ENVIRONMENTAL PROTECTION... § 52.426 Control strategy plans for attainment and rate-of-progress: ozone. (a) EPA fully approves, as... Delaware portion of the Philadelphia-Wilmington-Trenton severe ozone nonattainment, namely Kent and New...

Geostatistics as a validation tool for setting ozone standards for durum wheat.

PubMed

De Marco, Alessandra; Screpanti, Augusto; Paoletti, Elena

2010-02-01

Which is the best standard for protecting plants from ozone? To answer this question, we must validate the standards by testing biological responses vs. ambient data in the field. A validation is missing for European and USA standards, because the networks for ozone, meteorology and plant responses are spatially independent. We proposed geostatistics as validation tool, and used durum wheat in central Italy as a test. The standards summarized ozone impact on yield better than hourly averages. Although USA criteria explained ozone-induced yield losses better than European criteria, USA legal level (75 ppb) protected only 39% of sites. European exposure-based standards protected > or =90%. Reducing the USA level to the Canadian 65 ppb or using W126 protected 91% and 97%, respectively. For a no-threshold accumulated stomatal flux, 22 mmol m(-2) was suggested to protect 97% of sites. In a multiple regression, precipitation explained 22% and ozone explained <0.9% of yield variability. Copyright (c) 2009 Elsevier Ltd. All rights reserved.

An improved parameterisation of ozone dry deposition to the ocean and its impact in a global climate-chemistry model

NASA Astrophysics Data System (ADS)

Luhar, Ashok K.; Galbally, Ian E.; Woodhouse, Matthew T.; Thatcher, Marcus

2017-03-01

Schemes used to parameterise ozone dry deposition velocity at the oceanic surface mainly differ in terms of how the dominant term of surface resistance is parameterised. We examine three such schemes and test them in a global climate-chemistry model that incorporates meteorological nudging and monthly-varying reactive-gas emissions. The default scheme invokes the commonly used assumption that the water surface resistance is constant. The other two schemes, named the one-layer and two-layer reactivity schemes, include the simultaneous influence on the water surface resistance of ozone solubility in water, waterside molecular diffusion and turbulent transfer, and a first-order chemical reaction of ozone with dissolved iodide. Unlike the one-layer scheme, the two-layer scheme can indirectly control the degree of interaction between chemical reaction and turbulent transfer through the specification of a surface reactive layer thickness. A comparison is made of the modelled deposition velocity dependencies on sea surface temperature (SST) and wind speed with recently reported cruise-based observations. The default scheme overestimates the observed deposition velocities by a factor of 2-4 when the chemical reaction is slow (e.g. under colder SSTs in the Southern Ocean). The default scheme has almost no temperature, wind speed, or latitudinal variations in contrast with the observations. The one-layer scheme provides noticeably better variations, but it overestimates deposition velocity by a factor of 2-3 due to an enhancement of the interaction between chemical reaction and turbulent transfer. The two-layer scheme with a surface reactive layer thickness specification of 2.5 µm, which is approximately equal to the reaction-diffusive length scale of the ozone-iodide reaction, is able to simulate the field measurements most closely with respect to absolute values as well as SST and wind-speed dependence. The annual global oceanic deposition of ozone determined using this scheme is approximately half of the original oceanic deposition obtained using the default scheme, and it corresponds to a 10 % decrease in the original estimate of the total global ozone deposition. The previously reported modelled estimate of oceanic deposition is roughly one-third of total deposition and with this new parameterisation it is reduced to 12 % of the modelled total global ozone deposition. Deposition parameterisation influences the predicted atmospheric ozone mixing ratios, especially in the Southern Hemisphere. For the latitudes 45-70° S, the two-layer scheme improves the prediction of ozone observed at an altitude of 1 km by 7 % and that within the altitude range 1-6 km by 5 % compared to the default scheme.

The increasing threat to stratospheric ozone from dichloromethane.

PubMed

Hossaini, Ryan; Chipperfield, Martyn P; Montzka, Stephen A; Leeson, Amber A; Dhomse, Sandip S; Pyle, John A

2017-06-27

It is well established that anthropogenic chlorine-containing chemicals contribute to ozone layer depletion. The successful implementation of the Montreal Protocol has led to reductions in the atmospheric concentration of many ozone-depleting gases, such as chlorofluorocarbons. As a consequence, stratospheric chlorine levels are declining and ozone is projected to return to levels observed pre-1980 later this century. However, recent observations show the atmospheric concentration of dichloromethane-an ozone-depleting gas not controlled by the Montreal Protocol-is increasing rapidly. Using atmospheric model simulations, we show that although currently modest, the impact of dichloromethane on ozone has increased markedly in recent years and if these increases continue into the future, the return of Antarctic ozone to pre-1980 levels could be substantially delayed. Sustained growth in dichloromethane would therefore offset some of the gains achieved by the Montreal Protocol, further delaying recovery of Earth's ozone layer.

The increasing threat to stratospheric ozone from dichloromethane

NASA Astrophysics Data System (ADS)

Hossaini, Ryan; Chipperfield, Martyn P.; Montzka, Stephen A.; Leeson, Amber A.; Dhomse, Sandip S.; Pyle, John A.

2017-06-01

It is well established that anthropogenic chlorine-containing chemicals contribute to ozone layer depletion. The successful implementation of the Montreal Protocol has led to reductions in the atmospheric concentration of many ozone-depleting gases, such as chlorofluorocarbons. As a consequence, stratospheric chlorine levels are declining and ozone is projected to return to levels observed pre-1980 later this century. However, recent observations show the atmospheric concentration of dichloromethane--an ozone-depleting gas not controlled by the Montreal Protocol--is increasing rapidly. Using atmospheric model simulations, we show that although currently modest, the impact of dichloromethane on ozone has increased markedly in recent years and if these increases continue into the future, the return of Antarctic ozone to pre-1980 levels could be substantially delayed. Sustained growth in dichloromethane would therefore offset some of the gains achieved by the Montreal Protocol, further delaying recovery of Earth's ozone layer.

Ozone Layer Research and Technical Resources

EPA Pesticide Factsheets

Access information on research and technical resources related to ozone layer science. This page provides links to research efforts led by organizations such as the National Oceanic and Atmospheric Administration, the United Nations Environment Program, an

Ozone layer depletion simulation in an Environmental Chemistry course.

NASA Astrophysics Data System (ADS)

Cano, G. S.; Gavilán, I. C.; Garcia-Reynoso, J. A.; Santos, E.; Mendoza, A.; Perea, B.

2015-12-01

The reactions taking place between the ozone (O3) and various compounds present in the stratosphere has been studied extensively. When the balance between these reactions breakdown, destruction of ozone is favored. Here we create an experiment for and Environmental Chemistry laboratory course where students evaluate the ozone behavior by comparing its reactivity to various physical and chemical conditions; and observe the destruction of ozone by the action of halogenated compounds by means of volumetric technic. The conditions used are: (1) Ozone vs. Time; (2) Ozone + UV vs. Time; (3) Ozone + halogenated compound vs. Time; and (4) Ozone + UV + halogenated compound vs. Time. The results show that the O3 breaks down rapidly within about 25 min (Fig). They also explain the chemical reactions that occur in the destruction and generation of the ozone layer and demonstrate ozone depletion through the presence of halogenated compounds. The aim of this work is to bring the knowledge gained from theory into practice and thus the possibility of developing a critical attitude towards various environmental problems that arise today.

Is the Ozone Hole over Your Classroom?

ERIC Educational Resources Information Center

Cordero, Eugene C.

2002-01-01

Reports on a survey of first year university science students regarding their understanding of the ozone layer, ozone depletion, and the effect of ozone depletion on Australia. Suggests that better teaching resources for environmental issues such as ozone depletion and global warming are needed before improvements in student understanding can be…

Efficient ozone generator for ozone layer enrichment from high altitude balloon

NASA Technical Reports Server (NTRS)

Filiouguine, Igor V.; Kostiouchenko, Sergey V.; Koudriavtsev, Nikolay N.; Starikovskaya, Svetlana M.

1994-01-01

The possibilities of ozone production at low gas pressures by nanosecond high voltage discharge has been investigated. The measurements of ozone synthesis in N2-O2 mixtures have been performed. The explanation of experimental results is suggested. The possible ways of ozone yield growth are analyzed.

Effect of stratospheric aerosol layers on the TOMS/SBUV ozone retrieval

NASA Technical Reports Server (NTRS)

Torres, O.; Ahmad, Zia; Pan, L.; Herman, J. R.; Bhartia, P. K.; Mcpeters, R.

1994-01-01

An evaluation of the optical effects of stratospheric aerosol layers on total ozone retrieval from space by the TOMS/SBUV type instruments is presented here. Using the Dave radiative transfer model we estimate the magnitude of the errors in the retrieved ozone when polar stratospheric clouds (PSC's) or volcanic aerosol layers interfere with the measurements. The largest errors are produced by optically thick water ice PSC's. Results of simulation experiments on the effect of the Pinatubo aerosol cloud on the Nimbus-7 and Meteor-3 TOMS products are presented.

Measurements made aloft by a twin-engine aircraft to support the SCOS97-NARSTO study. Final report

DOE Office of Scientific and Technical Information (OSTI.GOV)

Anderson, J.A.; Blumenthal, D.L.

1999-05-01

During the summer of 1997, the Southern California Ozone Study (SCOS97) was conducted to update aerometric and emissions databases and model applications for ozone episodes in southern California and to quantify the contributions of interbasin transport to exceedances of the ozone standards in neighboring air basins. One of six SCOS97 sampling aircraft was a Piper Aztec. The Aztec performed northern-boundary measurements of aloft air quality and meteorology in the southern Mojave Desert and northern Los Angeles basin. The aircraft also served as a backup for another SCOS97 aircraft that performed flights in the western part of the study domain. Themore » Aztec data were reviewed to identify the occurrence and types of ozone layers aloft and to estimate the initial and boundary conditions in the Desert on the first day of Intensive Operational Periods (IOPs). Ozone carryover aloft was seen on all mornings in vertical spiral measurements in the Basin. Detached layers above the boundary layer were seen on about 20% of Basin morning and afternoon spirals. Offshore elevated ozone layers of up to 184 ppb were seen below 500 m. The morning ozone concentrations in the Desert ranged from 40 to 70 ppb and the Noy concentrations ranged from 2 to 4 ppb, indicating relatively clean, but not pristine boundary conditions.« less

[The relationship between the ozone layer and skin cancer].

PubMed

Sánchez C, Francisca

2006-09-01

In the recent decades, a sustained increase in the worldwide incidence of skin cancer has been observed and Chile is not the exception. The most important risk factor is the exaggerated and repeated exposure to ultraviolet radiation coming from the sun. The ozone layer restricts the transmission of type B and C ultraviolet light. Since 1980, a sustained depletion of stratospheric ozone levels is occurring, specially in middle latitudes (-30 to -60). Along with this depletion, the amount of ultraviolet light that reaches the earth surface is increasing. This article reviews some basic concepts about the ozone layer and the association between its depletion and skin cancer. The general population should be informed about the risks of inadequate and exaggerated exposure to sunlight.

Environmental effects of ozone depletion and its interactions with climate change: progress report, 2007.

PubMed

2008-01-01

This year the Montreal Protocol celebrates its 20th Anniversary. In September 1987, 24 countries signed the Montreal Protocol on Substances that Deplete the Ozone Layer. Today 191 countries have signed and have met strict commitments on phasing out of ozone depleting substances with the result that a 95% reduction of these substances has been achieved. The Montreal Protocol has also contributed to slowing the rate of global climate change, since most of the ozone depleting substances are also effective greenhouse gases. Even though much has been achieved, the future of the stratospheric ozone layer relies on full compliance of the Montreal Protocol by all countries for the remaining substances, including methyl bromide, as well as strict monitoring of potential risks from the production of substitute chemicals. Also the ozone depleting substances existing in banks and equipment need special attention to prevent their release to the stratosphere. Since many of the ozone depleting substances already in the atmosphere are long-lived, recovery cannot be immediate and present projections estimate a return to pre-1980 levels by 2050 to 2075. It has also been predicted that the interactions of the effects of the ozone layer and that of other climate change factors will become increasingly important.

Characterizing the seasonal cycle and vertical structure of ozone in Paris, France using four years of ground based LIDAR measurements in the lowermost troposphere

NASA Astrophysics Data System (ADS)

Klein, Amélie; Ancellet, Gérard; Ravetta, François; Thomas, Jennie L.; Pazmino, Andrea

2017-10-01

Systematic ozone LIDAR measurements were completed during a 4 year period (2011-2014) in Paris, France to study the seasonal variability of the vertical structure of ozone in the urban boundary layer. In addition, we use in-situ measurements from the surface air quality network that is located in Paris (AIRPARIF). Specifically, we use ozone and NO2 measurements made at two urban stations: Paris13 (60 m ASL) and the Eiffel Tower (310 m ASL) to validate and interpret the LIDAR profiles. Remote sensed tropospheric NO2 integrated columns from the SAOZ instrument located in Paris are also used to interpret ozone measurements. Comparison between ozone LIDAR measurements averaged from 250 m to 500 m and the Eiffel Tower in-situ measurements shows that the accuracy of the LIDAR (originally ±14 μg·m-3) is significantly improved (±7 μg·m-3) when a small telescope with a wide angular aperture is used. Results for the seasonal cycle of the ozone vertical gradient are found to be similar using two methods: (1) measured differences between AIRPARIF stations with measurements at 60 m ASL and 310 m ASL and (2) using LIDAR profiles from 300 m to the top of the Planetary Boundary Layer (PBL). Ozone concentrations measured by the LIDAR increase with altitude within the PBL, with a steeper gradient in winter (60 μg·m-3·km-1) and a less strong gradient in summer (20 μg·m-3·km-1). Results show that in winter, there is a sharp positive gradient of ozone at the surface, which is explained by ozone titration by NO combined with increased atmospheric stability in winter. In the afternoon during summer, photochemistry and vertical mixing are large enough to compensate for ozone titration near the surface, where NOx is emitted, and there is no gradient in ozone observed. In contrast, in the summer during the morning, ozone has a sharper positive vertical gradient similar to the winter values. Comparison of the vertically averaged ozone concentrations up to (0-3 km) and urban layer (0-310 m) ozone concentrations shows that the ratio between these two quantities is the largest in summer (86%) and the lowest in winter (49%). We conclude that satellite measurements that represent the 0-3 km integrated ozone column are not necessarily a good proxy for surface ozone and may lead to incorrect conclusions about the surface ozone seasonal variability. The ratio between the urban layer NO2 average concentration and the boundary layer NO2 average concentration obtained from SAOZ NO2 tropospheric columns is always less than 50%, meaning NO2 does not decrease linearly in the PBL, but with a sharper decrease close to the surface.

Convective forcing of mercury and ozone in the Arctic boundary layer induced by leads in sea ice.

PubMed

Moore, Christopher W; Obrist, Daniel; Steffen, Alexandra; Staebler, Ralf M; Douglas, Thomas A; Richter, Andreas; Nghiem, Son V

2014-02-06

The ongoing regime shift of Arctic sea ice from perennial to seasonal ice is associated with more dynamic patterns of opening and closing sea-ice leads (large transient channels of open water in the ice), which may affect atmospheric and biogeochemical cycles in the Arctic. Mercury and ozone are rapidly removed from the atmospheric boundary layer during depletion events in the Arctic, caused by destruction of ozone along with oxidation of gaseous elemental mercury (Hg(0)) to oxidized mercury (Hg(II)) in the atmosphere and its subsequent deposition to snow and ice. Ozone depletion events can change the oxidative capacity of the air by affecting atmospheric hydroxyl radical chemistry, whereas atmospheric mercury depletion events can increase the deposition of mercury to the Arctic, some of which can enter ecosystems during snowmelt. Here we present near-surface measurements of atmospheric mercury and ozone from two Arctic field campaigns near Barrow, Alaska. We find that coastal depletion events are directly linked to sea-ice dynamics. A consolidated ice cover facilitates the depletion of Hg(0) and ozone, but these immediately recover to near-background concentrations in the upwind presence of open sea-ice leads. We attribute the rapid recoveries of Hg(0) and ozone to lead-initiated shallow convection in the stable Arctic boundary layer, which mixes Hg(0) and ozone from undepleted air masses aloft. This convective forcing provides additional Hg(0) to the surface layer at a time of active depletion chemistry, where it is subject to renewed oxidation. Future work will need to establish the degree to which large-scale changes in sea-ice dynamics across the Arctic alter ozone chemistry and mercury deposition in fragile Arctic ecosystems.

Ozone Laminae and Their Entrainment Into a Valley Boundary Layer, as Observed From a Mountaintop Monitoring Station, Ozonesondes, and Aircraft Over California's San Joaquin Valley

NASA Astrophysics Data System (ADS)

Faloona, I. C.; Conley, S. A.; Caputi, D.; Trousdell, J.; Chiao, S.; Eiserloh, A. J., Jr.; Clark, J.; Iraci, L. T.; Yates, E. L.; Marrero, J. E.; Ryoo, J. M.; McNamara, M. E.

2016-12-01

The San Joaquin Valley of California is wide ( 75 km) and long ( 400 km), and is situated under strong atmospheric subsidence due, in part, to the proximity of the midlatitude anticyclone of the Pacific High. The capping effect of this subsidence is especially prominent during the warm season when ground level ozone is a serious air quality concern across the region. While relatively clean marine boundary layer air is primarily funneled into the valley below the strong subsidence inversion at significant gaps in the upwind Coast Range mountains, airflow aloft also spills over these barriers and mixes into the valley from above. Because this transmountain flow occurs under the influence of synoptic subsidence it tends to present discrete, laminar sheets of differing air composition above the valley boundary layer. Meanwhile, although the boundary layers tend to remain shallow due to the prevailing subsidence, orographic and anabatic venting of valley boundary layer air around the basin whips up a complex admixture of regional air masses into a "buffer layer" just above the boundary layer (zi) and below the lower free troposphere. We present scalar data of widely varying lifetimes including ozone, methane, NOx, and thermodynamic observations from upwind and within the San Joaquin Valley to better explain this layering and its subsequent erosion into the valley boundary layer via entrainment. Data collected at a mountaintop monitoring station on Chews Ridge in the Coast Range, by coastal ozonesondes, and aircraft are analyzed to document the dynamic layering processes around the complex terrain surrounding the valley. Particular emphasis will be made on observational methods whereby distal ozone can be distinguished from the regional ozone to better understand the influence of exogenous sources on air quality in the valley.

High Wintertime Ozone in the Uinta Basin: Diurnal Mixing and Ozone Production Measured by Tethered Ozonesondes

NASA Astrophysics Data System (ADS)

Johnson, B.; Cullis, P.; Schnell, R. C.; Oltmans, S. J.; Sterling, C. W.; Jordan, A. F.; Hall, E.

2016-12-01

Extreme high ozone mixing ratios, far exceeding U.S. National Air Quality Standards, were observed in the Uinta Basin in January-February 2013 under conditions highly favorable for wintertime ozone production. Hourly average ozone mixing ratios increased from regional background levels of 40-50 ppbv to >160 ppbv during several multi-day episodes of prolonged temperature inversions over snow-covered ground within air confining topography. Extensive surface and tethered balloon profile measurements of ozone, meteorology, CH4, CO2, NO2 and a suite of non-methane hydrocarbons (NMHCs) link emissions from oil and natural gas extraction with the strong ozone production throughout the Basin. High levels of NMHCs that were well correlated with CH4 showed that abundant O3 precursors were available throughout the Basin where high ozone mixing ratios extended from the surface to the top of the inversion layer at 200 m above ground level. This layer was at a nearly uniform height across the Basin even though there are significant terrain variations. Tethered balloon measurements rising above the elevated levels of ozone within the cold pool layer beneath the inversion measured regional background O3 concentrations. Surface wind and direction data from tethered balloons showed a consistent diurnal pattern in the Basin that moved air with the highest levels of CH4 and ozone precursor NMHC's from the gas fields of the east-central portion of the Basin to the edges during the day, before draining back into the Basin at night.

Enamel and dentin bond strength following gaseous ozone application.

PubMed

Cadenaro, Milena; Delise, Chiara; Antoniollo, Francesca; Navarra, Ottavia Chiara; Di Lenarda, Roberto; Breschi, Lorenzo

2009-08-01

To evaluate the effects of gaseous ozone application on enamel and dentin bond strength produced by two self-etching adhesive systems. The shear bond strength test was conducted to assess adhesion on enamel (protocol 1), while the microtensile bond strength test was performed on dentin (protocol 2). Protocol 1: 96 bovine incisors were randomly divided into 4 groups, and enamel surfaces were bonded in accordance with the following treatments: (1E) ozone + Clearfil Protect Bond; (2E) Clearfil Protect Bond (control); (3E) ozone + Xeno III; (4E) Xeno III (control). Ozone gas was applied for 80 s. Shear bond strength was measured with a universal testing machine. Protocol 2: 40 noncarious human molars were selected. Middle/deep dentin was exposed and bonded in accordance with the following treatments: (1D) ozone+Clearfil Protect Bond; (2D) Clearfil Protect Bond (control); (3D) ozone+Xeno III (4D) Xeno III (control). Four-mm-thick buildups were built on the adhesives, then specimens were sectioned in accordance with the nontrimming technique. Specimens were stressed until failure occurred, and failure modes were analyzed. Shear bond and microtensile bond strength data were analyzed using two-way ANOVA and Tukey's post-hoc test. No statistical differences were found between ozone treated specimens and controls, neither on enamel nor on dentin irrespective of the tested adhesive. Clearfil Protect Bond showed higher bond strength to enamel than Xeno III, irrespective of the ozone treatment (p < 0.05). The use of ozone gas to disinfect the cavity before placing a restoration had no influence on immediate enamel and dentin bond strength.

Role of Biomass Burning in the Formation of Tropospheric Ozone Laminae

NASA Astrophysics Data System (ADS)

Nair, U. S.; Wu, Y.; Kuang, S.; Newchurch, M.

2016-12-01

Laminar structure in free-tropospheric ozone profiles is a feature that is frequently observed in ozonesonde and lidar observations. Origins of these features are not well understood and have been linked to tropopause folding, stratospheric warming events and biomass burning emissions. Ozone laminae events with maximum ozone exceeding 80 ppb have been observed by the DIfferential Absorption Lidar (DIAL) instrument in Huntsville, Alabama. While many of the events are linked to tropopause folding, a subset of events located in the mid troposphere (2-6km) coincided with a smoke layer are associated with biomass burning. Satellite observations show the smoke originated from northwestern US wildfire events. Several of these ozone laminae associated with smoke have ozone excess of 20 ppb above the background values and have the potential to impact surface air quality if they enter the boundary layer. This presentation will report on process studies of ozone laminae associated with biomass burning plumes using A-Train satellite, ground based DIAL and ozonesonde observations. Fate and transport of the feature is also examined using WRFChem simulations, in specific transport into the boundary layer and impact on air quality at the surface.

Turbulent transport and production/destruction of ozone in a boundary layer over complex terrain

NASA Technical Reports Server (NTRS)

Greenhut, Gary K.; Jochum, Anne M.; Neininger, Bruno

1994-01-01

The first Intensive Observation Period (IOP) of the Swiss air pollution experiment POLLUMET took place in 1990 in the Aare River Valley between Bern and Zurich. During the IOP, fast response measurements of meteorological variables and ozone concentration were made within the boundary layer aboard a motorglider. In addition, mean values of meteorological variables and the concentrations of ozone and other trace species were measured using other aircraft, pilot balloons, tethersondes, and ground stations. Turbulent flux profiles of latent and sensible heat and ozone are calculated from the fast response data. Terms in the ozone mean concentration budget (time rate of change of mean concentration, horizontal advection, and flux divergence) are calculated for stationary time periods both before and after the passage of a cold front. The source/sink term is calculated as a residual in the budget, and its sign and magnitude are related to the measured concentrations of reactive trace species within the boundary layer. Relationships between concentration ratios of trace species and ozone concentration are determined in order to understand the influence of complex terrain on the processes that produce and destroy ozone.

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…

Natural and anthropogenic perturbations of the stratospheric ozone layer

NASA Technical Reports Server (NTRS)

Brasseur, Guy P.

1992-01-01

The paper reviews potential causes for reduction in the ozone abundance. The response of stratospheric ozone to solar activity is discussed. Ozone changes are simulated in relation with the potential development of a fleet of high-speed stratospheric aircraft and the release in the atmosphere of chlorofluorocarbons. The calculations are performed by a two-dimensional chemical-radiative-dynamical model. The importance of heterogeneous chemistry in polar stratospheric clouds and in the Junge layer (sulfate aerosol) is emphasized. The recently reported ozone trend over the last decade is shown to have been largely caused by the simultaneous effects of increasing concentrations of chlorofluorocarbons and heterogeneous chemistry. The possibility for a reduction in stratospheric ozone following a large volcanic eruption such as that of Mount Pinatubo in 1991 is discussed.

Why do Models Overestimate Surface Ozone in the Southeastern United States?

NASA Astrophysics Data System (ADS)

Travis, K.; Jacob, D.; Fisher, J. A.; Kim, S.; Marais, E. A.; Zhu, L.; Yu, K.; Miller, C. E.; Yantosca, R.; Payer Sulprizio, M.; Thompson, A. M.; Wennberg, P. O.; Crounse, J.; St Clair, J. M.; Cohen, R. C.; Laughner, J.; Dibb, J. E.; Hall, S. R.; Ullmann, K.; Wolfe, G.; Pollack, I. B.; Peischl, J.; Neuman, J. A.; Zhou, X.

2016-12-01

Ozone pollution in the Southeast US involves complex chemistry driven by emissions of anthropogenic nitrogen oxide radicals (NOx = NO + NO2) and biogenic isoprene. Model estimates of surface ozone concentrations tend to be biased high in the region and this is of concern for designing effective emission control strategies to meet air quality standards. We use detailed chemical observations from the SEAC4RS aircraft campaign in August and September 2013, interpreted with the GEOS-Chem chemical transport model at 0.25°×0.3125° horizontal resolution, to better understand the factors controlling surface ozone in the Southeast US. We find that the National Emission Inventory (NEI) for NO­x from the US Environmental Protection Agency (EPA) is too high in the Southeast and nationally by a factor of 2. This finding is based on SEAC4RS observations of NOx and its oxidation products, surface network observations of nitrate wet deposition fluxes, and OMI satellite observations of tropospheric NO2 columns. Upper tropospheric NO2 from lightning makes a large contribution to the satellite observations that must be accounted for when using these data to estimate surface NOx emissions. We find that only half of isoprene oxidation proceeds by the high-NOx pathway to produce ozone; this fraction is only moderately sensitive to changes in NOx emissions because isoprene and NOx emissions are spatially segregated. GEOS-Chem with reduced NOx emissions provides an unbiased simulation of ozone observations from the aircraft, and reproduces the observed ozone production efficiency in the boundary layer as derived from a regression of ozone and NOx oxidation products. However, the model is still biased high by 8±13 ppb relative to observed surface ozone in the Southeast US. Ozonesondes launched during midday hours show a 7 ppb ozone decrease from 1.5 km to the surface that GEOS-Chem does not capture. This may be caused by excessively dry conditions in the model, representing another factor important in the simulation of surface ozone.

The Effect of Ozone on Colonic Epithelial Cells.

PubMed

Himuro, Hidetomo

2018-05-21

Due to its strong oxidation activity, ozone has been well known to kill bacteria and exert toxic effects on human tissues. At the same time, ozone is being used for the treatment of diseases such as inflammatory bowel disease in some European countries. However, the use of ozone for therapeutic purposes, despite its strong toxic effects, remains largely unexplored. Interestingly, we found that intrarectal administration of ozone gas induced transient colonic epithelial cell damage characterized by the impairment of cell survival pathways involved in DNA replication, cell cycle, and mismatch repair. However, the damaged cells were rapidly extruded from the epithelial layer, and appeared to immediately stimulate turnover of the epithelial layer in the colon. Therefore, it is possible that ozone gas is able to trigger damage-induced rapid regeneration of intestinal epithelial cells, and that this explains why ozone does not cause harmful or persistent damage in the colon.

In situ correlative measurements for the ultraviolet differential absorption lidar and the high spectral resolution lidar air quality remote sensors: 1980 PEPE/NEROS program

NASA Technical Reports Server (NTRS)

Gregory, G. L.; Beck, S. M.; Mathis, J. J., Jr.

1981-01-01

In situ correlative measurements were obtained with a NASA aircraft in support of two NASA airborne remote sensors participating in the Environmental Protection Agency's 1980persistent elevated pollution episode (PEPE) and Northeast regional oxidant study (NEROS) field program in order to provide data for evaluating the capability of two remote sensors for measuring mixing layer height, and ozone and aerosol concentrations in the troposphere during the 1980 PEPE/NEROS program. The in situ aircraft was instrumented to measure temperature, dewpoint temperature, ozone concentrations, and light scattering coefficient. In situ measurements for ten correlative missions are given and discussed. Each data set is presented in graphical and tabular format aircraft flight plans are included.

Future local and remote influences on Mediterranean ozone air quality and climate forcing

NASA Astrophysics Data System (ADS)

Arnold, Steve; Martin, Maria Val; Emmons, Louisa; Rap, Alex; Heald, Colette; Lamarque, Jean-Francois; Tilmes, Simone

2013-04-01

The Mediterranean region is expected to display large increases in population over the coming decades, and to exhibit strong sensitivity to projected climate change, with increasing frequency of extreme summer temperatures and decreases in precipitation. Understanding of how these changes will affect atmospheric composition in the region is limited. The eastern Mediterranean basin has been shown to exhibit a pronounced summertime local maximum in tropospheric ozone, which impacts both local air quality and the atmospheric radiation balance. In summer, the region is subject to import of pollution from Northern Europe in the boundary layer and lower troposphere, from North American sources in the large-scale westerly flow of the free mid and upper-troposphere, as well as import of pollution lofted in the Asian monsoon and carried west to the eastern Mediterranean in anticyclonic flow in the upper troposphere over north Africa. In addition, interactions with the land-surface through biogenic emission sources and dry deposition play important roles in the Mediterranean ozone budget. Here we use the NCAR Community Earth System Model (CESM) to investigate how tropospheric ozone in the Mediterranean region responds to climate, land surface and global emissions changes between present day and 2050. We simulate climate and atmospheric composition for the year 2050, based on greenhouse gas abundances, trace gas and aerosol emissions and land cover and use from two representative concentration pathway (RCP) scenarios (RCP4.5 & RCP8.5), designed for use by the Coupled Model Intercomparison Project Phase 5(CMIP5) experiments in support of the IPCC. By comparing these simulations with a present-day scenario, we investigate the effects of predicted changes in climate and emissions on air quality and climate forcing over the Mediterranean region. The simulations suggest decreases in boundary layer ozone and sulfate aerosol throughout the tropospheric column over the Mediterranean under both RCP scenarios, and a significant increase in ozone between 5-10km. Using tagged regional NOy and tropospheric ozone tracers, we show that this ozone increase is coincident with an increase in easterly import of ozone and precursors in upper tropospheric outflow from Asian monsoon convection in 2050. We present a breakdown of the projected Mediterranean ozone changes by precursor source (anthropogenic and biogenic), and contributions due to changes in climate. Finally, we estimate the implications of the predicted changes in tropospheric composition for Mediterranean air quality and climate in 2050, and the consequences for the effectiveness of European policies aimed at protecting the region's climate and public health.

Report of a large depletion in the ozone layer over southern Brazil and Uruguay by using multi-instrumental data

NASA Astrophysics Data System (ADS)

Bresciani, Caroline; Dornelles Bittencourt, Gabriela; Valentin Bageston, José; Kirsch Pinheiro, Damaris; Schuch, Nelson Jorge; Bencherif, Hassan; Paes Leme, Neusa; Vaz Peres, Lucas

2018-03-01

Ozone is one of the chemical compounds that form part of the atmosphere. It plays a key role in the stratosphere where the ozone layer is located and absorbs large amounts of ultraviolet radiation. However, during austral spring (August-November), there is a massive destruction of the ozone layer, which is known as the Antarctic ozone hole. This phenomenon decreases ozone concentration in that region, which may affect other regions in addition to the polar one. This anomaly may also reach mid-latitudes; hence, it is called the secondary effect of the Antarctic ozone hole. Therefore, this study aims to identify the passage of an ozone secondary effect (OSE) event in the region of the city of Santa Maria - RS (29.68° S, 53.80° W) by means of a multi-instrumental analysis using the satellites TIMED/SABER, AURA/MLS, and OMI-ERS. Measurements were made in São Martinho da Serra/RS - Brazil (29.53° S, 53.85° W) using a sounding balloon and a Brewer Spectrophotometer. In addition, the present study aims to describe and analyse the influence that this stratospheric ozone reduction has on temperatures presented by these instruments, including data collected through the radio occultation technique. The event was first identified by the AURA/MLS satellite on 19 October 2016 over Uruguay. This reduction in ozone concentration was found by comparing the climatology for the years 1996-1998 for the state of Rio Grande do Sul, which is close to Uruguay. This event was already observed in Santa Maria/RS-Brazil on 20 October 2016 as presented by the OMI-ERS satellite and the Brewer Spectrophotometer. Moreover, a significant decrease was reported by the TIMED/SABER satellite in Uruguay. On 21 October, the poor ozone air mass was still over the region of interest, according to the OMI-ERS satellite, data from the sounding balloon launched in Santa Maria/RS-Brazil, and measurements made by the AURA/MLS satellite. Furthermore, the influence of ozone on the stratosphere temperature was observed during this period. Despite a continuous decrease detected in height, the temperature should have followed an increasing pattern in the stratospheric layer. Finally, the TIMED/SABER and OMI-ERS satellites showed that on 23 October, the air mass with low ozone concentration was moving away, and its layer, as well as the temperature, in the stratosphere was re-established.

Chemical effect on ozone deposition over seawater

EPA Science Inventory

Surface layer resistance plays an important role in determining ozone deposition velocity over seawater. Recent studies suggest that surface layer resistance over sea-water is influenced by wind-speed and chemical interaction at the air-water interface. Here, we investigate the e...

Photochemistry and dynamics of the ozone layer

NASA Technical Reports Server (NTRS)

Prinn, R. G.; Alyea, F. N.; Cunnold, D. M.

1978-01-01

The paper presents a broad review of the photochemical and dynamic theories of the ozone layer. The two theories are combined into the MIT three-dimensional dynamic-chemical quasi-geostrophic model with 26 levels in the vertical spaced in logarithmic pressure coordinates between the ground and 72-km altitude. The chemical scheme incorporates the important odd nitrogen, odd hydrogen, and odd oxygen chemistry, but is simplified in the sense that it requires specification of the distributions of NO2, OH and HO2. The prognostic equations are the vorticity equation, the perturbation thermodynamic equation, and the global mean and perturbation continuity equations for ozone; diagnostic equations include the hydrostatic equation, the balance condition, and the mass continuity equation. The model is applied to the investigation of the impact of supersonic aircraft on the ozone layer.

Evaluation of Day and Nighttime Lower Tropospheric Ozone from Air Quality Models using TES and Ozonesondes

NASA Astrophysics Data System (ADS)

Osterman, G. B.; Neu, J. L.; Eldering, A.; Pinder, R. W.; Tang, Y.; McQueen, J.

2012-12-01

At night, ozone can be transported long distances above the surface inversion layer without chemical destruction or deposition. As the boundary layer breaks up in the morning, this nocturnal ozone can be mixed down to the surface and rapidly increase ozone concentrations at a rate that can rival chemical ozone production. Most regional scale models that are used for air quality forecasts and ozone source attribution do not adequately capture nighttime ozone concentrations and transport. We combine ozone profile data from the NASA Earth Observing System (EOS) Tropospheric Emission Spectrometer (TES) and other sensors, ozonesonde data collected during the INTEX Ozonesonde Network Study (IONS), EPA AirNow ground station ozone data, the Community Multi-Scale Air Quality (CMAQ) model, and the National Air Quality Forecast Capability (NAQFC) model to examine air quality events during August 2006. We present both aggregated statistics and case-study analyses that assess the relationship between the models' ability to reproduce surface air quality events and their ability to capture the vertical distribution of ozone both during the day and at night. We perform the comparisons looking at the geospatial dependence in the differences between the measurements and models under different surface ozone conditions.

Lusaka, Zambia during SAFARI-2000: A Collection Point for Ozone Pollution

NASA Technical Reports Server (NTRS)

Thompson, Anne M.; Witte, Jacquelyn C.; Freiman, M. Tal; Phahlane, N. Agnes; Coetzee, G. J. R.; Bhartia, P. K. (Technical Monitor)

2002-01-01

In August and September, throughout south central Africa, seasonal clearing of dry vegetation and other fire-related activities lead to intense smoke haze and ozone formation. The first ozone soundings in the heart of the southern African burning region were taken at Lusaka, Zambia (155 deg S, 28 deg E) in early September 2000. Over 90 ppbv ozone was recorded at the surface (1.3 km elevation) and column tropospheric ozone was greater than 50 DU during a stagnant period. These values are much higher than concurrent measurements over Nairobi (1 deg S, 38 deg E) and Irene (25 deg S, 28 deg E, near Pretoria). The heaviest ozone pollution layer (800-500 hPa) over Lusaka is due to recirculated trans-boundary ozone. Starting out over Zambia, Angola, and Namibia, ozone heads east to the Indian Ocean, before turning back over Mozambique and Zimbabwe, heading toward Lusaka. Thus, Lusaka is a collection point for pollution, consistent with a picture of absolutely stable layers recirculating in a gyre over southern Africa.

Stratospheric ozone measurements at the equator

NASA Technical Reports Server (NTRS)

Ilyas, Mohammad

1994-01-01

A balloon-borne project for ozone layer measurements was undertaken using the MAST ozone sondes and ASTOR radiosondes. Previously published data on this series (Ilyas, 1984) was recently re-analyzed using a rigorous technique to evaluate correction factors (ranging between 1.2 to 1.4). The revised data presented here, show that at the tropospheric and lower stratospheric levels, the ozone concentrations at the equator are much lower than the mid-latitude concentrations. The layer of peak concentration is found to be shifted upward compared to the mid-latitude profile and above this the two profiles get closer.

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, the...

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 Alaska...

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 Alaska...

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 Alaska...

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, the...

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, the...

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 Alaska...

CANOZE measurements of the Arctic ozone hole

NASA Technical Reports Server (NTRS)

Evans, W. F. J.; Kerr, J. B.; Fast, H.

1988-01-01

In CANOZE 1 (Canadian Ozone Experiment), a series of 20 ozone profile measurements were made in April, 1986 from Alert at 82.5 N. CANOZE is the Canadian program for study of the Arctic winter ozone layer. In CANOZE 2, ozone profile measurements were made at Saskatoon, Edmonton, Churchill and Resolute during February and March, 1987 with ECC ozonesondes. Ground based measurements of column ozone, nitrogen dioxide and hydrochloric acid were conducted at Saskatoon. Two STRATOPROBE balloon flights were conducted on February 26 and March 19, 1987. Two aerosol flights were conducted by the University of Wyoming. The overall results of this study will be reported and compared with the NOZE findings. The results from CANOZE 3 in 1988, are also discussed. In 1988, as part of CANOZE 3, STRATOPROBE balloon flights were conducted from Saskatchewan on January 27 and February 13. A new lightweight infrared instrument was developed and test flown. A science flight was successfully conducted from Alert (82.5 N) on March 9, 1988 when the vortex was close to Alert; a good measurement of the profile of nitric acid was obtained. Overall, the Arctic spring ozone layer exhibits many of the features of the Antarctic ozone phenomenon, although there is obviously not a hole present every year. The Arctic ozone field in March, 1986 demonstrated many similarities to the Antarctic ozone hole. The TOMS imagery showed a crater structure in the ozone field similar to the Antarctic crater in October. Depleted layers of ozone were found in the profiles around 15 km, very similar to those reported from McMurdo. Enhanced levels of nitric acid were measured in air which had earlier been in the vortex. The TOMS imagery for March 1987 did not show an ozone crater, but will be examined for an ozone crater in February and March, 1988, the target date for the CANOZE 3 project.

Tropospheric Ozone Lidar Network (TOLNet) Observations of Processes Controlling Spatio-Temporal Tropospheric-Ozone Distributions

NASA Astrophysics Data System (ADS)

Newchurch, M.; Johnson, M. S.; Leblanc, T.; Langford, A. O.; Senff, C. J.; Kuang, S.; Strawbridge, K. B.; McGee, T. J.; Berkoff, T.; Chen, G.

2017-12-01

The Tropospheric Ozone Lidar Network, TOLNet, has matured into a credible scientific group of six ozone lidars that are capable of accurate, high-spatio-temporal-resolution measurement of tropospheric ozone structures and morphology These lidars have demonstrated their 10% accuracy in several intercomparison campaigns and have participated in several scientific investigations both in small and large instrumentation groups. They have investigated many scientific phenomena including stratosphere-to-troposphere exchange, boundary-layer development, the interaction between the boundary layer and the free troposphere, Front-range-ozone morphology, urban outflow, land/sea interactions, et al. These processes determine the ozone distribution affecting large portions of the population. The TOLNet group is now making significant contributions to the innovation of ozone lidar instrumentation and retrieval techniques. The campaigns proposed over the next few years build on demonstrated capability to address more difficult scientific issues, especially the ozone production potential and distribution from wildfires and prescribed burns. Through scientific cooperation with other ground-based profiling instrumentation, TOLNet is also contributing to the validation of the new measurement capabilities of TEMPO.

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

NASA Astrophysics Data System (ADS)

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

2010-12-01

The Montreal Protocol on Substances that Deplete the Ozone Layer was negotiated in 1987 and by 2010 had been signed by all of the nations of the world. In this presentation we use a fully coupled radiation-chemical-dynamical model to simulate a future world where ozone depletion substances (ODSs) were never regulated. In this “world avoided” simulation, ODS levels increase by 3% per year. From 1980 to 2020 we find that 17% of the globally average column ozone is destroyed, and from 1980 to 2065 67% is destroyed. Severe polar depletions (e.g., the Antarctic ozone hole) become year-round rather than just seasonal. 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 lower stratospheric upwelling. In response to ozone changes, ultraviolet (UV) radiation increases, tripling the erythemal (sunburn) radiation in the northern summer mid-latitudes by 2065.

Incorporation of multiple cloud layers for ultraviolet radiation modeling studies

NASA Technical Reports Server (NTRS)

Charache, Darryl H.; Abreu, Vincent J.; Kuhn, William R.; Skinner, Wilbert R.

1994-01-01

Cloud data sets compiled from surface observations were used to develop an algorithm for incorporating multiple cloud layers into a multiple-scattering radiative transfer model. Aerosol extinction and ozone data sets were also incorporated to estimate the seasonally averaged ultraviolet (UV) flux reaching the surface of the Earth in the Detroit, Michigan, region for the years 1979-1991, corresponding to Total Ozone Mapping Spectrometer (TOMS) version 6 ozone observations. The calculated UV spectrum was convolved with an erythema action spectrum to estimate the effective biological exposure for erythema. Calculations show that decreasing the total column density of ozone by 1% leads to an increase in erythemal exposure by approximately 1.1-1.3%, in good agreement with previous studies. A comparison of the UV radiation budget at the surface between a single cloud layer method and a multiple cloud layer method presented here is discussed, along with limitations of each technique. With improved parameterization of cloud properties, and as knowledge of biological effects of UV exposure increase, inclusion of multiple cloud layers may be important in accurately determining the biologically effective UV budget at the surface of the Earth.

Nighttime mesospheric ozone enhancements during the 2002 southern hemispheric major stratospheric warming

NASA Astrophysics Data System (ADS)

Smith-Johnsen, Christine; Orsolini, Yvan; Stordal, Frode; Limpasuvan, Varavut; Pérot, Kristell

2018-03-01

Sudden Stratospheric Warmings (SSW) affect the chemistry and dynamics of the middle atmosphere. Major warmings occur roughly every second winter in the Northern Hemisphere (NH), but has only been observed once in the Southern Hemisphere (SH), during the Antarctic winter of 2002. Observations by the Global Ozone Monitoring by Occultation of Stars (GOMOS, an instrument on board Envisat) during this rare event, show a 40% increase of ozone in the nighttime secondary ozone layer at subpolar latitudes compared to non-SSW years. This study investigates the cause of the mesospheric nighttime ozone increase, using the National Center for Atmospheric Research (NCAR) Whole Atmosphere Community Climate Model with specified dynamics (SD-WACCM). The 2002 SH winter was characterized by several reductions of the strength of the polar night jet in the upper stratosphere before the jet reversed completely, marking the onset of the major SSW. At the time of these wind reductions, corresponding episodic increases can be seen in the modelled nighttime secondary ozone layer. This ozone increase is attributed largely to enhanced upwelling and the associated cooling of the altitude region in conjunction with the wind reversal. This is in correspondence to similar studies of SSW induced ozone enhancements in NH. But unlike its NH counterpart, the SH secondary ozone layer appeared to be impacted less by episodic variations in atomic hydrogen. Seasonally decreasing atomic hydrogen plays however a larger role in SH compared to NH.

Convective and Wave Signatures in Ozone Profiles Over the Equatorial Americas: Views from TC4 (2007) and SHADOZ

NASA Technical Reports Server (NTRS)

Thompson, Anne M.; MacFarlane, Alaina M.; Morris, Gary A.; Yorks, John E.; Miller, Sonya K.; Taubman, Brett F.; Verver, Ge; Voemel, Holger; Avery, Melody A.; Hair, Johnathan W.;

Volcanic aerosol and ozone depletion within the Antarctic polar vortex during the austral spring of 1991

DOE Office of Scientific and Technical Information (OSTI.GOV)

Deshler, T.; Adriani, A.; Gobbi, G.P.

1992-09-01

In the spring of 1991 the Antarctic lower stratosphere was characterized by a layer of volcanic aerosol from the Cerro Hudson eruption. This aerosol layer was observed from McMurdo Station, Antarctica, with both lidar and balloonborne particle counters beginning around 10 September. After 20 September the aerosol was observed daily between 9 and 13 km. In this layer homogeneous nucleation of new aerosol was observed with concentrations greater than 6000/cu cm. Comparisons of scattering ratio calculated from measured particle size distributions agree best with the lidar measurements when a real index of refraction near 1.5 is used. In the pastmore » 5 years of measurements, ozone below 13 km has been relatively unchanged during the annual Antartic ozone depletion; however, in 1991 ozone below 13 km decreased at a rate of 4 - 8 ppb/day over 30 days. This change began shortly after the appearance of the volcanic aerosol, providing direct measurements correlating volcanic aerosol and ozone depletion. 16 refs.« less

40 CFR 82.124 - Prohibitions.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Prohibitions. 82.124 Section 82.124 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone-Depleting Substances § 82.124 Prohibitions. (a) Warning...

40 CFR 82.122 - Certification, recordkeeping, and notice requirements.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Certification, recordkeeping, and notice requirements. 82.122 Section 82.122 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone...

40 CFR 82.120 - Petitions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 17 2011-07-01 2011-07-01 false Petitions. 82.120 Section 82.120 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone-Depleting Substances § 82.120 Petitions. (a...

40 CFR 82.122 - Certification, recordkeeping, and notice requirements.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 17 2011-07-01 2011-07-01 false Certification, recordkeeping, and notice requirements. 82.122 Section 82.122 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone...

40 CFR 82.124 - Prohibitions.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 17 2011-07-01 2011-07-01 false Prohibitions. 82.124 Section 82.124 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone-Depleting Substances § 82.124 Prohibitions. (a) Warning...

40 CFR 82.120 - Petitions.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Petitions. 82.120 Section 82.120 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone-Depleting Substances § 82.120 Petitions. (a...

Simple model for estimating dry deposition velocity of ozone and its destruction in a polluted nocturnal boundary layer

NASA Astrophysics Data System (ADS)

Lin, Ching-Ho; Lai, Chin-Hsing; Wu, Yee-Lin; Chen, Ming-Jen

2010-11-01

Determining the destructions of both ozone and odd oxygen, O x, in the nocturnal boundary layer (NBL) is important to evaluate the regional ozone budget and overnight ozone accumulation. This work develops a simple method to determine the dry deposition velocity of ozone and its destruction at a polluted nocturnal boundary layer. The destruction of O x can also be determined simultaneously. The method is based on O 3 and NO 2 profiles and their surface measurements. Linkages between the dry deposition velocities of O 3 and NO 2 and between the dry deposition loss of O x and its chemical loss are constructed and used. Field measurements are made at an agricultural site to demonstrate the application of the model. The model estimated nocturnal O 3 dry deposition velocities from 0.13 to 0.19 cm s -1, very close to those previously obtained for similar land types. Additionally, dry deposition and chemical reactions account for 60 and 40% of the overall nocturnal ozone loss, respectively; ozone dry deposition accounts for 50% of the overall nocturnal loss of O x, dry deposition of NO 2 accounts for another 20%, and chemical reactions account for the remaining 30%. The proposed method enables the use of measurements made in typical ozone field studies to evaluate various nocturnal destructions of O 3 and O x in a polluted environment.

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 PM2.5...

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 PM2.5...

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 PM2.5...

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 PM2.5...

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 PM2.5...

20 Years of Total and Tropical Ozone Time Series Based on European Satellite Observations

NASA Astrophysics Data System (ADS)

Loyola, D. G.; Heue, K. P.; Coldewey-Egbers, M.

2016-12-01

Ozone is an important trace gas in the atmosphere, while the stratospheric ozone layer protects the earth surface from the incident UV radiation, the tropospheric ozone acts as green house gas and causes health damages as well as crop loss. The total ozone column is dominated by the stratospheric column, the tropospheric columns only contributes about 10% to the total column.The ozone column data from the European satellite instruments GOME, SCIAMACHY, OMI, GOME-2A and GOME-2B are available within the ESA Climate Change Initiative project with a high degree of inter-sensor consistency. The tropospheric ozone columns are based on the convective cloud differential algorithm. The datasets encompass a period of more than 20 years between 1995 and 2015, for the trend analysis the data sets were harmonized relative to one of the instruments. For the tropics we found an increase in the tropospheric ozone column of 0.75 ± 0.12 DU decade^{-1} with local variations between 1.8 and -0.8. The largest trends were observed over southern Africa and the Atlantic Ocean. A seasonal trend analysis led to the assumption that the increase is caused by additional forest fires.The trend for the total column was not that certain, based on model predicted trend data and the measurement uncertainty we estimated that another 10 to 15 years of observations will be required to observe a statistical significant trend. In the mid latitudes the trends are currently hidden in the large variability and for the tropics the modelled trends are low. Also the possibility of diverging trends at different altitudes must be considered; an increase in the tropospheric ozone might be accompanied by decreasing stratospheric ozone.The European satellite data record will be extended over the next two decades with the atmospheric satellite missions Sentinel 5 Precursor (launch end of 2016), Sentinel 4 and Sentinel 5.

Impact Assessment of Global Temperature Perturbations on Urban and Regional Ozone Levels in South Texas

NASA Astrophysics Data System (ADS)

Biswas, Jhumoor; John, Kuruvilla; Farooqui, Zuber

The recent Intergovernmental Panel on Climate Change report predicts significant temperature increases over the century which constitutes the pulse of climate variability in a region. A modeling study was performed to identify the potential impact of temperature perturbations on tropospheric ozone concentrations in South Texas. A future case modeling scenario which incorporates appropriate emission reduction strategies without accounting for climatic inconsistencies was used in this study. The photochemical modeling was undertaken for a high ozone episode of 13-20 September 1999, and a future modeling scenario was projected for ozone episode days in 2007 utilizing the meteorological conditions prevalent in the base year. The temperatures were increased uniformly throughout the simulation domain and through the vertical layers by 2°C, 3°C, 4°C, 5°C, and 6°C, respectively in the future year modeling case. These temperature perturbations represented the outcome of extreme climate change within the study region. Significantly large changes in peak ozone concentrations were predicted by the photochemical model. For the 6°C temperature perturbation, the greatest amplification in the maximum 8-h ozone concentrations within urban areas of the modeling domain was approximately 12 ppb. In addition, transboundary flux from major industrialized urban areas played a major role in supplementing the high ozone concentrations during the perturbed temperature scenarios. The Unites States Environmental Protection Agency (USEPA) is currently proposing stricter 8-h ozone standards. The effect of temperature perturbations on ozone exceedances based on current and potential stringent future National Ambient Air Quality Standards (NAAQS) was also studied. Temperatures had an appreciable spatial impact on the 8-h ozone exceedances with a considerable increase in spatial area exceeding the NAAQS for the 8-h ozone levels within the study region for each successive augmentation in temperature. The number of exceedances of the 8-h ozone standard increased significantly with each degree rise of temperature with the problem becoming even more acute in light of stricter future proposed standards of ozone.

40 CFR 82.102 - Applicability.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 18 2012-07-01 2012-07-01 false Applicability. 82.102 Section 82.102 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone-Depleting Substances § 82.102 Applicability. (a) In the...

40 CFR 82.102 - Applicability.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 17 2011-07-01 2011-07-01 false Applicability. 82.102 Section 82.102 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone-Depleting Substances § 82.102 Applicability. (a) In the...

40 CFR 82.102 - Applicability.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 18 2013-07-01 2013-07-01 false Applicability. 82.102 Section 82.102 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone-Depleting Substances § 82.102 Applicability. (a) In the...

40 CFR 82.102 - Applicability.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Applicability. 82.102 Section 82.102 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone-Depleting Substances § 82.102 Applicability. (a) In the...

40 CFR 82.102 - Applicability.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 18 2014-07-01 2014-07-01 false Applicability. 82.102 Section 82.102 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone-Depleting Substances § 82.102 Applicability. (a) In the...

Vertical distribution and sources of tropospheric ozone over South China in spring 2004: Ozonesonde measurements and modeling analysis

NASA Astrophysics Data System (ADS)

Zhang, Y.; Liu, H.; Crawford, J. H.; Considine, D. B.; Chan, C.; Scientific Team Of Tapto

2010-12-01

The Transport of Air Pollutant and Tropospheric Ozone over China (TAPTO-China) science initiative is a two-year (TAPTO 2004 and 2005) field measurement campaign to help improve our understanding of the physical and chemical processes that control the tropospheric ozone budget over the Chinese subcontinent (including the Asian Pacific rim) and its surrounding SE Asia. In this paper, we use two state-of-the-art 3-D global chemical transport models (GEOS-Chem and Global Modeling Initiative or GMI) to examine the characteristics of vertical distribution and quantify the sources of tropospheric ozone by analysis of TAPTO in-situ ozonesonde data obtained at five stations in South China during spring (April and May) 2004: Lin’an (30.30N, 119.75E), Tengchong (25.01N, 98.30E), Taipei (25.0N, 121.3E), Hong Kong (22.21N, 114.30E) and Sanya (18.21N, 110.31E). The observed tropospheric ozone concentrations show strong spatial and temporal variability, which is largely captured by the models. The models simulate well the observed vertical gradients of tropospheric ozone at higher latitudes but are too low at lower latitudes. Model tagged ozone simulations suggest that stratosphere has a large impact on the upper and middle troposphere (UT/MT) at Lin’an and Tengchong. Continental SE Asian biomass burning emissions are maximum in March but still contribute significantly to the photochemical production of tropopheric ozone in South China in early April. Asian anthropogenic emissions are the major contribution to lower tropospheric ozone at all stations. On the other hand, there are episodes of influence from European/North American anthropogenic emissions. For example, model tagged ozone simulations show that over Lin’an in April 2004, stratosphere contributes 20% (13 ppbv) at 5 km, Asian boundary layer contributes 70% (46 ppbv) to ozone in the boundary layer, European boundary layer contributes 5% (3-4 ppbv) at 1.2 km, and North American boundary layer contributes 4.5% (3 ppbv) at 1.2 km. Lastly, our analysis suggests that lightning NOx emissions have substantial impact on the UT/MT ozone over South China. We argue that model underestimate of ozone concentrations, especially at lower latitudes, is likely due to too low lightning NOx emissions.

40 CFR 97.1 - Purpose.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Purpose. 97.1 Section 97.1 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) FEDERAL NOX... transport of ozone and nitrogen oxides, an ozone precursor. ...

40 CFR 82.110 - Form of label bearing warning statement.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Form of label bearing warning statement. 82.110 Section 82.110 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone-Depleting...

40 CFR 82.112 - Removal of label bearing warning statement.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Removal of label bearing warning statement. 82.112 Section 82.112 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) PROTECTION OF STRATOSPHERIC OZONE The Labeling of Products Using Ozone-Depleting...

SAGE 2-Umkehr case study of ozone differences and aerosol effects from October 1984 to April 1989

NASA Technical Reports Server (NTRS)

Newchurch, M. J.; Cunnold, D. M.

1994-01-01

A comparison of 1262 cases of coincident ozone profiles derived from 666 Umkehrs at 17 different stations and 901 SAGE 2 profiles within 1000 km and 12 hours between October 1984 and April 1989 indicates the following layer percentage differences with 2-sigma error bars: layer three 14.6 plus/minus 3.3 percent, layer four 17.6 plus/minus 1.1 percent, layer five -1.3 plus/minus 0.5 percent, layer six -5.7 plus/minus 0.7 percent, layer seven -1.0 plus/minus 0.7 percent, layer eight 4.2 plus/minus 0.7 percent, and layer nine 6.8 plus/minus 1.2 percent. Comparing SAGE 2-Umkehr differences to SAGE 1 version 5.5-Umkehr differences shows SAGE 2 higher than or equal to SAGE 1 relative to Umkehr in all layers except layer three. Adjustment for this bias would produce trends derived from SAGE 2-SAGE 1 differences and Umkehr observations in the 1980s more nearly equal to each other in layers six, seven, and eight. A possible explanation of these differences is a systematic shift in the reference altitude between SAGE 1 and SAGE 2, but there is no independent evidence of this. While the shape of the vertical profile of differences at 17 individual Umkehr stations (mostly in mid-latitudes) is generally consistent at all stations except at Poker Flat, Seoul, and Lauder, significant variation does exists among the stations. The profile of mean difference is similar to previously observed differences between Umkehr and both SAGE 2 and SBUV and also to an eigenvector analysis, but with site-dependent amplitude discrepancies. Because of the close correspondence of stratospheric aerosol optical depth at the SAGE 2-measured 0.525 micron wavelength and the extrapolated 0.32 Umkehr wavelength determined in this study, we use the 0.525 micron data to determine the aerosol effect of Umkehr profiles. The aerosol errors to the Umkehr ozone amounts in percent ozone amount per 0.01 stratospheric aerosol optical depth range from plus 2 percent in layer six to minus 3 percent in layer nine. These results agree with previous theoretical and empirical studies within their respective error bounds in layers nine, eight, and five. The result in layer six differs significantly from previous works. In view of the fact that SAGE 2 and Umkehr produce different ozone retrievals in layers eight and nine and because the intra-layer correlation of SAGE 2 ozone and aerosol in layers eight and nine in non-zero, one must exercise some caution in attributing the entire SAGE 2-Umkehr differences in the upper layers to an aerosol effect.

Reconciliation of Halogen-Induced Ozone Loss with the Total-Column Ozone Record

NASA Technical Reports Server (NTRS)

Shepherd, T. G.; Plummer, D. A.; Scinocca, J. F.; Hegglin, M. I.; Fioletov, V. E.; Reader, M. C.; Remsberg, E.; von Clarmann, T.; Wang, H. J.

2014-01-01

The observed depletion of the ozone layer from the 1980s onwards is attributed to halogen source gases emitted by human activities. However, the precision of this attribution is complicated by year-to-year variations in meteorology, that is, dynamical variability, and by changes in tropospheric ozone concentrations. As such, key aspects of the total-column ozone record, which combines changes in both tropospheric and stratospheric ozone, remain unexplained, such as the apparent absence of a decline in total-column ozone levels before 1980, and of any long-term decline in total-column ozone levels in the tropics. Here we use a chemistry-climate model to estimate changes in halogen-induced ozone loss between 1960 and 2010; the model is constrained by observed meteorology to remove the eects of dynamical variability, and driven by emissions of tropospheric ozone precursors to separate out changes in tropospheric ozone. We show that halogen-induced ozone loss closely followed stratospheric halogen loading over the studied period. Pronounced enhancements in ozone loss were apparent in both hemispheres following the volcanic eruptions of El Chichon and, in particular, Mount Pinatubo, which significantly enhanced stratospheric aerosol loads. We further show that approximately 40% of the long-term non-volcanic ozone loss occurred before 1980, and that long-term ozone loss also occurred in the tropical stratosphere. Finally, we show that halogeninduced ozone loss has declined by over 10% since stratospheric halogen loading peaked in the late 1990s, indicating that the recovery of the ozone layer is well underway.

Graphene Oxide by UV-Ozone Treatment as an Efficient Hole Extraction Layer for Highly Efficient and Stable Polymer Solar Cells.

PubMed

Xia, Yingdong; Pan, Yufeng; Zhang, Haijuan; Qiu, Jian; Zheng, Yiting; Chen, Yonghua; Huang, Wei

2017-08-09

The hole extraction layer has a significant impact on the achievement of high-efficiency polymer solar cells (PSCs). Here, we report an efficient approach to direct UV-ozone treatment by larger device performance enhancement employing graphene oxide (GO). The dramatic performance enhancement of PSCs with the P3HT:PCBM blend as an active layer was demonstrated by the UV-ozone treatment of GO for 30 min: best power conversion efficiency (PCE) of 4.18%, fill factor of 0.63, J sc of 10.94 mA cm -2 , and V oc of 0.61 V, which are significantly higher than those of the untreated GO (1.82%) and highly comparable PEDOT:PSS-based PSCs (3.73%). In addition, PSCs with UV-ozone-treated GO showed a longer stability than PSCs with PEDOT:PSS. The significant enhancement of PCEs of PSCs can be attributed to the fact that ozone molecules can oxidize GO into CO 2 and leave highly conductive graphene particles. We suggest that this simple UV-ozone treatment can provide an efficient method for highly efficient GO hole extraction in high-performance PSCs.

Lidar Atmospheric Observatory in the Canadian Arctic

NASA Technical Reports Server (NTRS)

Ulitsky, Arkady; Wang, Tin-Yu; Flood, Martin; Smith, Brent

1992-01-01

During the last decade there have been growing concerns about a broad variety of atmospheric properties. Among these, a depletion of the stratospheric ozone layer has attracted considerable attention from the general public, politicians and scientists due to its vital impact for the entire global biosphere. One of the major warning signs was the discovery of the 'ozone hole' in the Antarctic region where the concentration of the ozone in the stratosphere was significantly reduced. At present the stratospheric ozone layer in this region is being continuously monitored by groups of scientists from around the world and numerous observations of the ozone layer on the global scale have clearly demonstrated the process of ozone depletion. Recent observations by NASA have shown significant depletion in the Arctic region. This paper provides an initial description of two lidars that are planned to be installed in a new observatory for atmospheric studies in the Canadian Arctic. This observatory is being constructed under the supervision of the Atmospheric Environment Services (AES) of Canada as a part of Green Plan - an initiative of the Federal Government of Canada. The station is located at Eureka on Ellesmere Island at a latitude of 80 degrees N and a longitude of 86 degrees W.

US EPA Nonattainment Areas and Designations-8 Hour Ozone (2008 NAAQS)

EPA Pesticide Factsheets

This web service contains the following layers: Ozone 2008 NAAQS NAA State Level and Ozone 2008 NAAQS NAA National Level. Full FGDC metadata records for each layer may be found by clicking the layer name at the web service endpoint (https://gispub.epa.gov/arcgis/rest/services/OAR_OAQPS/NAA2008Ozone8hour/MapServer) and viewing the layer description. These layers identify areas in the U.S. where air pollution levels have not met the National Ambient Air Quality Standards (NAAQS) for criteria air pollutants and have been designated nonattainment?? areas (NAA). The data are updated weekly from an OAQPS internal database. However, that does not necessarily mean the data have changed. The EPA Office of Air Quality Planning and Standards (OAQPS) has set National Ambient Air Quality Standards for six principal pollutants, which are called criteria pollutants. Under provisions of the Clean Air Act, which is intended to improve the quality of the air we breathe, EPA is required to set National Ambient Air Quality Standards for six common air pollutants. These commonly found air pollutants (also known as criteria pollutants) are found all over the United States. They are particle pollution (often referred to as particulate matter), ground-level ozone, carbon monoxide, sulfur oxides, nitrogen oxides, and lead. For each criteria pollutant, there are specific procedures used for measuring ambient concentrations and for calculating long-term (quarterly or annual) and/or short-

US EPA Nonattainment Areas and Designations-8 Hour Ozone (1997 NAAQS)

EPA Pesticide Factsheets

This web service contains the following layers: Ozone 1997 NAAQS NAA State Level and Ozone 1997 NAAQS NAA National Level. Full FGDC metadata records for each layer may be found by clicking the layer name at the web service endpoint (https://gispub.epa.gov/arcgis/rest/services/OAR_OAQPS/NAA1997Ozone8hour/MapServer) and viewing the layer description. These layers identify areas in the U.S. where air pollution levels have not met the National Ambient Air Quality Standards (NAAQS) for criteria air pollutants and have been designated nonattainment?? areas (NAA). The data are updated weekly from an OAQPS internal database. However, that does not necessarily mean the data have changed. The EPA Office of Air Quality Planning and Standards (OAQPS) has set National Ambient Air Quality Standards for six principal pollutants, which are called criteria pollutants. Under provisions of the Clean Air Act, which is intended to improve the quality of the air we breathe, EPA is required to set National Ambient Air Quality Standards for six common air pollutants. These commonly found air pollutants (also known as criteria pollutants) are found all over the United States. They are particle pollution (often referred to as particulate matter), ground-level ozone, carbon monoxide, sulfur oxides, nitrogen oxides, and lead. For each criteria pollutant, there are specific procedures used for measuring ambient concentrations and for calculating long-term (quarterly or annual) and/or short

Aircraft measurement of ozone turbulent flux in the atmospheric boundary layer

NASA Astrophysics Data System (ADS)

Affre, Ch.; Carrara, A.; Lefebre, F.; Druilhet, A.; Fontan, J.; Lopez, A.

In May 1995, the "Chimie-Creil 95" experiment was undertaken in the north of France. The field data are first used to validate the methodology for airborne measurement of ozone flux. A certain number of methodological problems due to the location of the fast ozone sensor inside the airplane are, furthermore discussed. The paper describes the instrumentation of the ARAT (Avion de Recherche Atmosphérique et de Télédétection), an atmospheric research and remote-sensing aircraft used to perform the airborne measurements, the area flown over, the meteorological conditions and boundary layer stability conditions. These aircraft measurements are then used to determine ozone deposition velocity and values are proposed for aerodynamic, bulk transfer coefficients (ozone and momentum). The paper also establishes the relationship between the normalised standard deviation and stability parameters ( z/ L) for ozone, temperature, humidity and vertical velocity. The laws obtained are then presented.

A Multi-wavelength Ozone Lidar for the EASOE Experiment

NASA Technical Reports Server (NTRS)

Godin, S.; Ancellet, G.; David, C.; Porteneuve, J.; Leroy, C.; Mitev, V.; Emery, Y.; Flesia, C.; Rizi, V.; Visconti, G.

1992-01-01

The study of the ozone layer during winter and springtime in high latitude regions is a major issue in atmospheric research. For a better understanding of these problems, an important experimental campaign called EASOE (European Arctic Stratospheric Ozone Experiment) was organized by the European Community during the winter 1991-1992. Its main objective was to establish a budget of the ozone destruction processes on the whole northern hemisphere. This implied the simultaneous operation of different types of instruments located in both high and mid-latitude regions in order to study the destruction processes as well as the evolution of the ozone layer during the period of the campaign. A description will be given here of a mobile ozone lidar instrument specially designed for operation during the EASOE campaign. This system, which performs ozone measurements in the 5 to 40 km altitude range was located in Sodankyla, Finland as part of the ELSA experiment which also includes operation of another multi-wavelength lidar designed for polar stratospheric cloud measurements.

Modification of the optoelectronic properties of two-dimensional MoS2 crystals by ultraviolet-ozone treatment

NASA Astrophysics Data System (ADS)

Yang, Hae In; Park, Seonyoung; Choi, Woong

2018-06-01

We report the modification of the optoelectronic properties of mechanically-exfoliated single layer MoS2 by ultraviolet-ozone exposure. Photoluminescence emission of pristine MoS2 monotonically decreased and eventually quenched as ultraviolet-ozone exposure time increased from 0 to 10 min. The reduction of photoluminescence emission accompanied reduction of Raman modes, suggesting structural degradation in ultraviolet-ozone exposed MoS2. Analysis with X-ray photoelectron spectroscopy revealed that the formation of Ssbnd O and Mosbnd O bonding increases with ultraviolet-ozone exposure time. Measurement of electrical transport properties of MoS2 in a bottom-gate thin-film transistor configuration suggested the presence of insulating MoO3 after ultraviolet-ozone exposure. These results demonstrate that ultraviolet-ozone exposure can significantly influence the optoelectronic properties of single layer MoS2, providing important implications on the application of MoS2 and other two-dimensional materials into optoelectronic devices.

A modelling case study to evaluate control strategies for ozone reduction in Southwestern Spain

NASA Astrophysics Data System (ADS)

Castell, N.; Mantilla, E.; Salvador, R.; Stein, A. F.; Millán, M.

2009-09-01

Ozone is a strong oxidant and when certain concentrations are reached it has adverse effects on health, vegetation and materials. With the aim of protecting human health and ecosystems, European Directive 2008/50/EC establishes target values for ozone concentrations, to be achieved from 2010 onwards. In our study area, located in southwestern Spain, ozone levels regularly exceed the human health protection threshold defined in the European Directive. Indeed, this threshold was exceeded on 92 days in 2007, despite the fact that the Directive stipulates that it should not be exceeded on more than 25 days per calendar year averaged over three years. It is urgent, therefore, to reduce the current ozone levels, but because ozone is a secondary pollutant, this reduction must necessarily involve limiting the emission of its precursors, primarily nitrogen oxides (NOx) and volatile organic compounds (VOC). During the central months of the year, southwestern Spain is under strong insolation and weak synoptic forcing, promoting the development of sea breezes and mountain-induced winds and creating re-circulations of pollutants. The complex topography of the area induces the formation of vertical layers, into which the pollutants are injected and subjected to long distance transport and compensatory subsidence. The characteristics of these highly complex flows have important effects on the pollutant dispersion. In this study two ozone pollution episodes have been selected to assess the ozone response to reductions in NOx and VOC emissions from industry and traffic. The first corresponds to a typical summer episode, with the development of breezes in an anticyclonic situation with low gradient pressure and high temperatures, while the second episode presents a configuration characteristic of spring or early summer, with a smooth westerly flow and more moderate temperatures. Air pollution studies in complex terrain require the use of high-resolution models to resolve the complex structures of the local flows and their impact on emissions; nevertheless, these mesoscale systems are developed within the scope of a synoptic circulation, which also affects both the breeze development and the pollutant transport. In order to take the relationship between the different atmospheric scales into account, we used the CAMx photochemical model coupled with the MM5 meteorological model, both configured with a system of nested grids. The study domain covers an area of 28224 km2, with 2 km horizontal resolution and 18 vertical layers up to a height of 5 km with high resolution in the levels close to the ground. This paper assesses the impact over the hourly and 8-hourly maximum daily ozone concentrations of four reduction strategies in an area with complex terrain: (i) 25% reduction in VOC and NOx from industry and traffic, (ii) 50% reduction in NOx and VOC from the industry, (iii) 50% reduction in NOx and VOC from traffic, and (iv) 100% reduction in NOx and VOC from the petrochemical plant and the refinery. The study area has large industrial sources, such as a petroleum refinery, a petrochemical plant, several chemical complexes and co-generation power plants, among others. The study area includes the cities of Huelva (148,000 inhabitants), Seville (699,760 inhabitants) and Cadiz (127,200 inhabitants). The analyses presented in this work provide an assessment of the effectiveness of several strategies to reduce ozone pollution in different meteorological scenarios.

Diurnal variations and source apportionment of ozone at the summit of Mount Huang, a rural site in Eastern China.

PubMed

Gao, J; Zhu, B; Xiao, H; Kang, H; Hou, X; Yin, Y; Zhang, L; Miao, Q

2017-03-01

Comprehensive measurements were conducted at the summit of Mount (Mt.) Huang, a rural site located in eastern China during the summer of 2011. They observed that ozone showed pronounced diurnal variations with high concentrations at night and low values during daytime. The Weather Research and Forecasting with Chemistry (WRF-Chem) model was applied to simulate the ozone concentrations at Mt. Huang in June 2011. With processes analysis and online ozone tagging method we coupled into the model system, the causes of this diurnal pattern and the contributions from different source regions were investigated. Our results showed that boundary layer diurnal cycle played an important role in driving the ozone diurnal variation. Further analysis showed that the negative contribution of vertical mixing was significant, resulting in the ozone decrease during the daytime. In contrast, ozone increased at night owing to the significant positive contribution of advection. This shifting of major factor between vertical mixing and advection formed this diurnal variation. Ozone source apportionment results indicated that approximately half was provided by inflow effect of ozone from outside the model domain (O 3-INFLOW ) and the other half was formed by ozone precursors (O 3-PBL ) emitted in eastern, central, and southern China. In the O 3-PBL , 3.0% of the ozone was from Mt. Huang reflecting the small local contribution (O 3-LOC ) and the non-local contributions (O 3-NLOC ) accounted for 41.6%, in which ozone from the southerly regions contributed significantly, for example, 9.9% of the ozone originating from Jiangxi, representing the highest geographical contributor. Because the origin and variation of O 3-NLOC was highly related to the diurnal movements in boundary layer, the similar diurnal patterns between O 3-NLOC and total ozone both indicated the direct influence of O 3-NLOC and the importance of boundary layer diurnal variations in the formation of such distinct diurnal ozone variations at Mt. Huang. Copyright © 2016 Elsevier Ltd. All rights reserved.

[Climatic changes in Scandinavia--consequences for public health].

PubMed

Kanestrøm, I

1999-01-30

Atmospheric composition and climate conditions are of great importance for health. Increasing consumption of fossil fuels ever since the industrial revolution has resulted in higher contents of greenhouse gases in the atmosphere. Primarily, this will increase the global temperature. Secondarily, it may change the patterns of precipitation and droughts. Higher extreme temperatures will have a negative effect on health. Climate changes can also change the living conditions of undesirable insects and microbes. The ozone gas in the atmosphere acts as a shield against the harmful ultraviolet radiation from the sun. Chlorofluorocarbons contribute to reduction of the ozone layer and increase ultraviolet radiation. Increased exposure of the skin to this radiation may cause damage such as sunburn and skin cancer. In order to avoid damage, it is of importance to wear protective clothing or use effective sunshades.

Extensive halogen-mediated ozone destruction over the tropical Atlantic Ocean.

PubMed

Read, Katie A; Mahajan, Anoop S; Carpenter, Lucy J; Evans, Mathew J; Faria, Bruno V E; Heard, Dwayne E; Hopkins, James R; Lee, James D; Moller, Sarah J; Lewis, Alastair C; Mendes, Luis; McQuaid, James B; Oetjen, Hilke; Saiz-Lopez, Alfonso; Pilling, Michael J; Plane, John M C

2008-06-26

Increasing tropospheric ozone levels over the past 150 years have led to a significant climate perturbation; the prediction of future trends in tropospheric ozone will require a full understanding of both its precursor emissions and its destruction processes. A large proportion of tropospheric ozone loss occurs in the tropical marine boundary layer and is thought to be driven primarily by high ozone photolysis rates in the presence of high concentrations of water vapour. A further reduction in the tropospheric ozone burden through bromine and iodine emitted from open-ocean marine sources has been postulated by numerical models, but thus far has not been verified by observations. Here we report eight months of spectroscopic measurements at the Cape Verde Observatory indicative of the ubiquitous daytime presence of bromine monoxide and iodine monoxide in the tropical marine boundary layer. A year-round data set of co-located in situ surface trace gas measurements made in conjunction with low-level aircraft observations shows that the mean daily observed ozone loss is approximately 50 per cent greater than that simulated by a global chemistry model using a classical photochemistry scheme that excludes halogen chemistry. We perform box model calculations that indicate that the observed halogen concentrations induce the extra ozone loss required for the models to match observations. Our results show that halogen chemistry has a significant and extensive influence on photochemical ozone loss in the tropical Atlantic Ocean boundary layer. The omission of halogen sources and their chemistry in atmospheric models may lead to significant errors in calculations of global ozone budgets, tropospheric oxidizing capacity and methane oxidation rates, both historically and in the future.

Spaceship Nigeria: A Topic Study for Global Warming, Greenhouse Effect and Ozone Layer Depletion.

ERIC Educational Resources Information Center

Okebukola, Peter; Akpan, Ben B.

1997-01-01

Explains the concept of a topic study, how it meets the needs of teachers seeking to integrate their teaching, and how it is especially well suited for environmental education. Outlines curriculum for a topic study on the greenhouse effect and ozone layer depletion. (DDR)

Reaction rates of graphite with ozone measured by etch decoration

NASA Technical Reports Server (NTRS)

Hennig, G. R.; Montet, G. L.

1968-01-01

Etch-decoration technique of detecting vacancies in graphite has been used to determine the reaction rates of graphite with ozone in the directions parallel and perpendicular to the layer planes. It consists essentially of peeling single atom layers off graphite crystals without affecting the remainder of the crystal.

Student Teacher Understanding of the Greenhouse Effect, Ozone Layer Depletion, and Acid Rain.

ERIC Educational Resources Information Center

Dove, Jane

1996-01-01

Describes the results of a survey designed to ascertain details of student teachers' knowledge and misconceptions about the greenhouse effect, acid rain, and ozone layer depletion. Results indicate familiarity with the issues but little understanding of the concepts involved and many commonly held misconceptions. (JRH)

The Extrapolar SWIFT model (version 1.0): fast stratospheric ozone chemistry for global climate models

NASA Astrophysics Data System (ADS)

Kreyling, Daniel; Wohltmann, Ingo; Lehmann, Ralph; Rex, Markus

2018-03-01

The Extrapolar SWIFT model is a fast ozone chemistry scheme for interactive calculation of the extrapolar stratospheric ozone layer in coupled general circulation models (GCMs). In contrast to the widely used prescribed ozone, the SWIFT ozone layer interacts with the model dynamics and can respond to atmospheric variability or climatological trends.The Extrapolar SWIFT model employs a repro-modelling approach, in which algebraic functions are used to approximate the numerical output of a full stratospheric chemistry and transport model (ATLAS). The full model solves a coupled chemical differential equation system with 55 initial and boundary conditions (mixing ratio of various chemical species and atmospheric parameters). Hence the rate of change of ozone over 24 h is a function of 55 variables. Using covariances between these variables, we can find linear combinations in order to reduce the parameter space to the following nine basic variables: latitude, pressure altitude, temperature, overhead ozone column and the mixing ratio of ozone and of the ozone-depleting families (Cly, Bry, NOy and HOy). We will show that these nine variables are sufficient to characterize the rate of change of ozone. An automated procedure fits a polynomial function of fourth degree to the rate of change of ozone obtained from several simulations with the ATLAS model. One polynomial function is determined per month, which yields the rate of change of ozone over 24 h. A key aspect for the robustness of the Extrapolar SWIFT model is to include a wide range of stratospheric variability in the numerical output of the ATLAS model, also covering atmospheric states that will occur in a future climate (e.g. temperature and meridional circulation changes or reduction of stratospheric chlorine loading).For validation purposes, the Extrapolar SWIFT model has been integrated into the ATLAS model, replacing the full stratospheric chemistry scheme. Simulations with SWIFT in ATLAS have proven that the systematic error is small and does not accumulate during the course of a simulation. In the context of a 10-year simulation, the ozone layer simulated by SWIFT shows a stable annual cycle, with inter-annual variations comparable to the ATLAS model. The application of Extrapolar SWIFT requires the evaluation of polynomial functions with 30-100 terms. Computers can currently calculate such polynomial functions at thousands of model grid points in seconds. SWIFT provides the desired numerical efficiency and computes the ozone layer 104 times faster than the chemistry scheme in the ATLAS CTM.

On the role of atmosphere-ocean interactions in the expected long-term changes of the Earth's ozone layer caused by greenhouse gases

NASA Astrophysics Data System (ADS)

Zadorozhny, Alexander; Dyominov, Igor

It is well known that anthropogenic emissions of greenhouse gases into the atmosphere produce a global warming of the troposphere and a global cooling of the stratosphere. The expected stratospheric cooling essentially influences the ozone layer via increased polar stratospheric cloud formation and via temperature dependences of the gas phase reaction rates. One more mechanism of how greenhouse gases influences the ozone layer is enhanced water evaporation from the oceans into the atmosphere because of increasing temperatures of the ocean surface due to greenhouse effect. The subject of this paper is a study of the influence of anthropogenic pollution of the atmosphere by the greenhouse gases CO2, CH4, N2O and ozone-depleting chlorine and bromine compounds on the expected long-term changes of the ozone layer with taking into account an increase of water vapour content in the atmosphere due to greenhouse effect. The study based on 2-D zonally averaged interactive dynamical radiative-photochemical model of the troposphere and stratosphere. The model allows to self-consistently calculating 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 two types. It was supposed in the model that an increase of the ocean surface temperature caused by greenhouse effect is similar to calculated increase of atmospheric surface temperature. Evaporation rate from the ocean surface was computed in dependence of latitude. The model time-dependent runs were made for the period from 1975 to 2100 using two IPCC scenarios depicting maximum and average expected increases of greenhouse gases in the atmosphere. The model calculations show that anthropogenic increasing of water vapour abundance in the atmosphere due to heating of the ocean surface caused by greenhouse effect gives a sensible contribution to the expected ozone changes. The enhanced evaporation from the ocean increases noticeably a water vapour abundance in the stratosphere that decreases global total ozone and retards the expected recovery of the ozone layer. In polar latitudes, additional stratospheric water vapour increase due to greenhouse effect noticeably strengthens the impact of anthropogenic greenhouse gases on ozone through modification of polar stratospheric clouds and retards the expected recovery of the ozone, too. In the Northern hemisphere, the delay of the ozone recovery is about 5 years, in the Southern hemisphere the delay is about 2 years.

New Insights on "Next Day" Ozone Increases in the Northeastern U.S. using Continuous Vertical Profiles of Ozone

NASA Astrophysics Data System (ADS)

Sullivan, J. T.; McGee, T. J.; Rabenhorst, S. D.; Delgado, R.; Dreessen, J.; Sumnicht, G. K.; Twigg, L.

2016-12-01

A unique multi-day air quality event occurred throughout the Mid-Atlantic region from June 9-12, 2015. The June event was coupled to the advection of widespread smoke and debris from western Canada throughout the region. Observations indicated that the aged smoke impacted the Planetary Boundary Layer (PBL) and greatly enhanced ozone concentrations at the surface. Many ground sites in the region, particularly in Maryland, recorded 8-hr ozone concentrations that were in exceedance of the 75 ppb EPA National Ambient Air Quality Standard (NAAQS). After the high O3 episode occurred, a nocturnal low-level jet developed throughout the Mid-Atlantic region, which was spatially correlated with next day high O3 at several sites within the New England region. During this event, nearly continuous vertical profiles of ozone are presented at Beltsville, MD from the NASA Goddard Space Flight Center TROPospheric OZone DIfferential Absorption Lidar (GSFC TROPOZ DIAL), which has been developed and validated within the Tropospheric Ozone Lidar Network (TOLNet). Lidar observations reveal a well-mixed polluted PBL, nocturnal residual layer, and subsequent mixing down of the residual layer in the morning. Additional measurements of surface ozone, aerosol lidar profiles, wind profiles, and balloon borne profiles are also presented. Model output and trajectory analyses are also presented to illustrate the complex flow regimes that occurred during the daytime and nighttime to help redistribute the polluted air mass.

77 FR 46755 - Notification of a Public Meeting of the Clean Air Scientific Advisory Committee (CASAC) Ozone...

Federal Register 2010, 2011, 2012, 2013, 2014

2012-08-06

... Scientific Advisory Committee (CASAC) Ozone Review Panel AGENCY: Environmental Protection Agency (EPA... the CASAC Ozone Review Panel to conduct a peer review of EPA's Integrated Science Assessment for Ozone... Assessment for Ozone--First External Review Draft (July 2012), Welfare Risk and Exposure Assessment for Ozone...

Inclusion of the second Umkehr in the conventional Umkehr retrieval analysis as a means of improving ozone retrievals in the upper stratosphere

NASA Technical Reports Server (NTRS)

Gioulgkidis, Konstantinos; Lowe, Robert P.; Mcelroy, C. Tom

1994-01-01

The Umkehr method for retrieving the gross features of the vertical ozone distribution requires measurements of the ratio of zenith-sky radiances at two wavelengths in the near-UV region while the solar zenith angle (SZA) changes from 60 to 90 degrees. A Brewer spectrophotometer was used for taking such measurements extending the SZA range down to 96 degrees. Analyzed data from the Spring of 1991 imply that observations at twilight are of great significance in improving ozone retrievals in the upper stratosphere. Judged by the variance reduction for Umkehr layers 9 to 12 (25-30 percent for layer 11) and the increase in separation and amplitude of the averaging kernels for the relevant layers, the ozone retrievals in the upper stratosphere are shown to be in better agreement with climatological means.

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 contributes significantly to the daily variation of surface maximum ozone concentrations (R2 = 0.19). However, the contribution of downward-mixing ozone to daily ozone variation is not included in most existing statistical models developed for predicting daily ozone variation. Finally, daily surface maximum ozone concentration is positively correlated with daily afternoon mixing depth, attributable to the downward-mixing ozone.

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.

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 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 be...

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 be...

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 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 be...

40 CFR 52.582 - Control strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control strategy: Ozone. 52.582 Section 52.582 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED...—The Administrator approves the incorporation of the photochemical assessment ambient monitoring system...

Scientific assessment of ozone depletion: 1991

NASA Technical Reports Server (NTRS)

1991-01-01

Over the past few years, there have been highly significant advances in the understanding of the impact of human activities on the Earth's stratospheric ozone layer and the influence of changes in chemical composition of the radiative balance of the climate system. Specifically, since the last international scientific review (1989), there have been five major advances: (1) global ozone decreases; (2) polar ozone; (3) ozone and industrial halocarbons; (4) ozone and climate relations; and (5) ozone depletion potentials (ODP's) and global warming potentials (GWP's). These topics and others are discussed.

California Baseline Ozone Transport Study (CABOTS): Ozonesonde Measurements

NASA Astrophysics Data System (ADS)

Eiserloh, A. J., Jr.; Chiao, S.; Spitze, J.; Cauley, S.; Clark, J.; Roberts, M.

2016-12-01

Because the EPA recently lowered the ambient air quality standard for the 8-hr average of ozone (O3) to70 ppbv, California must continue to achieve significant reductions in ozone precursor emissions and prepare for new State Implementation Plans (SIP) to demonstrate how ground-level ambient ozone will be reduced below the new health-based standard. Prior studies suggest that background levels of ozone traveling across the Pacific Ocean can significantly influence surface ozone throughout California, particularly during the spring. Evidence has been presented indicating that background levels of ozone continue to increase in the western United States over the recent few decades, implying more ozone exceedances in the future. To better understand the contributions of the external natural and anthropogenic pollution sources as well as atmospheric processes for surface ozone concentrations in California during the spring and summer months, the California Baseline Ozone Transport Study (CABOTS) has been established. One major goal of CABOTS is to implement near daily ozonesonde measurements along the California Coast to quantify background ozone aloft before entering the State during high ozone season. CABOTS has been ongoing from May through August of 2016 launching ozonesondes from Bodega Bay and Half Moon Bay, California. The temporal progression of ozonesonde measurements and subsequent analysis of the data will be discussed with a focus on the contribution of background ozone to surface ozone sites inland as well as likely origins of layers aloft. Comparisons of current ozonesondes versus prior ozonesonde studies of California will also be performed. A few selected cases of high ozone layers moving onshore from different sources will be discussed as well.

ROLE OF NITROGEN OXIDES IN NONURBAN OZONE FORMATION IN THE PLANETARY BOUNDARY LAYER OVER N (NORTH) AMERICA, W (WESTERN) EUROPE AND ADJACENT AREAS OF OCEAN

EPA Science Inventory

The status of knowledge on photochemical ozone formation and the effects of nitrogen oxides and peroxyacyl nitrates on such formation has been evaluated. The literature is reviewed on nonurban ozone and nitrogen oxide concentration distributions, ozone lifetimes, nitrogen oxide l...

Airborne Dial Remote Sensing of the Arctic Ozone Layer

NASA Technical Reports Server (NTRS)

Wirth, Martin; Renger, Wolfgang; Ehret, Gerhard

1992-01-01

A combined ozone and aerosol LIDAR was developed at the Institute of Physics of the Atmosphere at the DLR in Oberpfaffenhofen. It is an airborne version, that, based on the DIAL-principle, permits the recording of two-dimensional ozone profiles. This presentation will focus on the ozone-part; the aerosol subsection will be treated later.

An intercomparison of multidecadal observational and reanalysis data sets for global total ozone trends and variability analysis

NASA Astrophysics Data System (ADS)

Bai, Kaixu; Chang, Ni-Bin; Shi, Runhe; Yu, Huijia; Gao, Wei

2017-07-01

A four-step adaptive ozone trend estimation scheme is proposed by integrating multivariate linear regression (MLR) and ensemble empirical mode decomposition (EEMD) to analyze the long-term variability of total column ozone from a set of four observational and reanalysis total ozone data sets, including the rarely explored ERA-Interim total ozone reanalysis, from 1979 to 2009. Consistency among the four data sets was first assessed, indicating a mean relative difference of 1% and root-mean-square error around 2% on average, with respect to collocated ground-based total ozone observations. Nevertheless, large drifts with significant spatiotemporal inhomogeneity were diagnosed in ERA-Interim after 1995. To emphasize long-term trends, natural ozone variations associated with the solar cycle, quasi-biennial oscillation, volcanic aerosols, and El Niño-Southern Oscillation were modeled with MLR and then removed from each total ozone record, respectively, before performing EEMD analyses. The resulting rates of change estimated from the proposed scheme captured the long-term ozone variability well, with an inflection time of 2000 clearly detected. The positive rates of change after 2000 suggest that the ozone layer seems to be on a healing path, but the results are still inadequate to conclude an actual recovery of the ozone layer, and more observational evidence is needed. Further investigations suggest that biases embedded in total ozone records may significantly impact ozone trend estimations by resulting in large uncertainty or even negative rates of change after 2000.

Long-term uvb forecasting on the basis of spectral and broad-band measurements

NASA Astrophysics Data System (ADS)

Bérces, A.; Gáspár, S.; Kovács, G.; Rontó, G.

2003-04-01

The stratospheric ozone concentration has been investigated by several methods, e.g. determinations of the ozone layer using a network of ground based spectrophotometers, of the Dobson and the Brewer types. These data indicate significant decrease of the ozone layer superimposed by much larger seasonal changes at specific geographical locations. The stratospheric ozone plays an important role in the attenuation of the short-wavelength components of the solar spectrum, thus the consequence of the decreased ozone layer is an increased UVB level. Various pyranometers measuring the biological effect of environmental UV radiation have been constructed with spectral sensitivities close to the erythema action spectrum defined by the CIE. Using these erythemally weighted broad-band instruments to detect the tendency of UVB radiation controversial data have been found. To quantify the biological risk due to environmental UV radiation it is reasonable to weight the solar spectrum by the spectral sensitivity of the DNA damage taking into account the high DNA-sensitivity at the short wavelength range of the solar spectrum. Various biological dosimeters have been developed e.g. polycrystalline uracil thin layer. These are usually simple biological systems or components of them. Their UV sensitivity is a consequence of the DNA-damage. Biological dosimeters applied for long-term monitoring are promising tools for the assessment of the biological hazard. Simultaneous application of uracil dosimeters and Robertson-Berger meters can be useful to predict the increasing tendency of the biological UV exposure more precisely. The ratio of the biologically effective dose obtained by the uracil dosimeter (a predominately UVB effect) and by the Robertson-Berger meter (insensitive to changes below 300 nm) is a sensitive method for establishing changes in UVB irradiance due to changes in ozone layer.

40 CFR 52.930 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.930 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Kentucky § 52.930 Control strategy: Ozone. (a) The VOC..., Campbell and Kenton Counties) ozone nonattainment area. The demonstration of attainment of the ozone...

40 CFR 52.1885 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.1885...: Ozone. (a) Part D—Approval. The following portions of the Ohio plan are approved: (1) The ozone portions...: Akron, Canton, Cincinnati, Cleveland, Columbus, Dayton, Toledo and Youngstown. (4) The ozone...

40 CFR 52.2235 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.2235... strategy: Ozone. (a) Determination—EPA is determining that, as of August 8, 1995, the Nashville ozone nonattainment area has attained the ozone standard and that the reasonable further progress and attainment...

40 CFR 52.1885 - Control strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.1885...: Ozone. (a) Part D—Approval. The following portions of the Ohio plan are approved: (1) The ozone portions...: Akron, Canton, Cincinnati, Cleveland, Columbus, Dayton, Toledo and Youngstown. (4) The ozone...

40 CFR 52.1885 - Control strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.1885...: Ozone. (a) Part D—Approval. The following portions of the Ohio plan are approved: (1) The ozone portions...: Akron, Canton, Cincinnati, Cleveland, Columbus, Dayton, Toledo and Youngstown. (4) The ozone...

40 CFR 52.1885 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.1885...: Ozone. (a) Part D—Approval. The following portions of the Ohio plan are approved: (1) The ozone portions...: Akron, Canton, Cincinnati, Cleveland, Columbus, Dayton, Toledo and Youngstown. (4) The ozone...

40 CFR 52.930 - Control strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.930 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Kentucky § 52.930 Control strategy: Ozone. (a) The VOC..., Campbell and Kenton Counties) ozone nonattainment area. The demonstration of attainment of the ozone...

40 CFR 52.2235 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.2235... strategy: Ozone. (a) Determination—EPA is determining that, as of August 8, 1995, the Nashville ozone nonattainment area has attained the ozone standard and that the reasonable further progress and attainment...

40 CFR 52.930 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.930 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Kentucky § 52.930 Control strategy: Ozone. (a) The VOC..., Campbell and Kenton Counties) ozone nonattainment area. The demonstration of attainment of the ozone...

40 CFR 52.1885 - Control strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Ozone. 52.1885...: Ozone. (a) Part D—Approval. The following portions of the Ohio plan are approved: (1) The ozone portions...: Akron, Canton, Cincinnati, Cleveland, Columbus, Dayton, Toledo and Youngstown. (4) The ozone...

40 CFR 52.1023 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.1023...: Ozone. (a) Determination. EPA is determining that, as of July 21, 1995, the Lewiston-Auburn ozone nonattainment area has attained the ozone standard and that the reasonable further progress and attainment...

40 CFR 52.1023 - Control strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.1023...: Ozone. (a) Determination. EPA is determining that, as of July 21, 1995, the Lewiston-Auburn ozone nonattainment area has attained the ozone standard and that the reasonable further progress and attainment...

40 CFR 52.1023 - Control strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.1023...: Ozone. (a) Determination. EPA is determining that, as of July 21, 1995, the Lewiston-Auburn ozone nonattainment area has attained the ozone standard and that the reasonable further progress and attainment...

40 CFR 52.2235 - Control strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 5 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.2235... strategy: Ozone. (a) Determination—EPA is determining that, as of August 8, 1995, the Nashville ozone nonattainment area has attained the ozone standard and that the reasonable further progress and attainment...

40 CFR 52.930 - Control strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.930 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Kentucky § 52.930 Control strategy: Ozone. (a) The VOC..., Campbell and Kenton Counties) ozone nonattainment area. The demonstration of attainment of the ozone...

40 CFR 52.2235 - Control strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Ozone. 52.2235... strategy: Ozone. (a) Determination—EPA is determining that, as of August 8, 1995, the Nashville ozone nonattainment area has attained the ozone standard and that the reasonable further progress and attainment...

40 CFR 52.2235 - Control strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 5 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.2235... strategy: Ozone. (a) Determination—EPA is determining that, as of August 8, 1995, the Nashville ozone nonattainment area has attained the ozone standard and that the reasonable further progress and attainment...

40 CFR 52.1023 - Control strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Ozone. 52.1023...: Ozone. (a) Determination. EPA is determining that, as of July 21, 1995, the Lewiston-Auburn ozone nonattainment area has attained the ozone standard and that the reasonable further progress and attainment...

40 CFR 52.930 - Control strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control strategy: Ozone. 52.930 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Kentucky § 52.930 Control strategy: Ozone. (a) The VOC..., Campbell and Kenton Counties) ozone nonattainment area. The demonstration of attainment of the ozone...

40 CFR 52.1023 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.1023...: Ozone. (a) Determination. EPA is determining that, as of July 21, 1995, the Lewiston-Auburn ozone nonattainment area has attained the ozone standard and that the reasonable further progress and attainment...

Global Warming and Ozone Layer Depletion: STS Issues for Social Studies Classrooms.

ERIC Educational Resources Information Center

Rye, James A.; Strong, Donna D.; Rubba, Peter A.

2001-01-01

Explores the inclusion of science-technology-society (STS) education in social studies. Provides background information on global warming and the depletion of the ozone layer. Focuses on reasons for teaching global climate change in the social studies classroom and includes teaching suggestions. Offers a list of Web sites about global climate…

Knowledge about the Greenhouse Effect and the Effects of the Ozone Layer among Norwegian Pupils Finishing Compulsory Education in 1989, 1993, and 2005—What Now?

NASA Astrophysics Data System (ADS)

Kirkeby Hansen, Pål J.

2010-02-01

The greenhouse effect and the effects of the ozone layer have been in the media and public focus for more than two decades. During the same period, Norwegian compulsory schools have had four national curricula. The two last-mentioned prescribe explicitly the two topics. Media and public discourse might have been sources of information causing informal learning among pupils. The point of departure for this questionnaire-based examination of the development of pupils' knowledge about the greenhouse effect and the effects of the ozone layer from 1989 to 2005 is the changing curricula and formal and informal learning. In 2005 the trends seem to be that more pupils confuse the greenhouse effect with the effects of the ozone layer. At the same time, specific knowledge about the greenhouse effect is improving. This article will discuss some possible causes for these trends, and give some recommendations for teaching the topics in accordance with the last national curriculum implemented in 2006.

Mesoscale circulation systems and ozone concentrations during ESCOMPTE: a case study from IOP 2b

NASA Astrophysics Data System (ADS)

Kalthoff, N.; Kottmeier, C.; Thürauf, J.; Corsmeier, U.; Saїd, F.; Fréjafon, E.; Perros, P. E.

2005-03-01

The main objective of 'Expérience sur Site pour COntraindre les Modèles de Pollution atmosphérique et de Transport d'Emissions' (ESCOMPTE) is to generate a relevant data set for testing and evaluating mesoscale chemistry-transport models (CTMs). During ESCOMPTE, measurements have been performed at numerous surface stations, by radars and lidars, and several aircraft in the planetary boundary layer. The data from these different sources have been merged to obtain a consistent description of the spatial distribution of wind, temperature, humidity, and ozone for the photosmog episode on June 25, 2001 (IOP 2b). On this day, moderate synoptic winds favour the evolution of different mesoscale circulation systems. During daytime, the sea breeze penetrates towards the north in the Rhône valley. As the winds above the sea breeze layer come from the east, polluted air from the metropolitan area of Marseille leads to an increase of ozone at elevated layers above the convective boundary layer (CBL). At the mountainous station of Luberon about 55 km north of Marseille around noon, when the CBL top surpasses the height of the mountain summit, polluted air with ozone concentrations of about 120 ppbv arrived from southerly directions, thus indicating the passage of the city plume of Marseille. At Cadarache and Vinon in the Durance valley, about 60 km inland, the ozone maximum at the surface and at flight level 920 m MSL appears between 14 and 15 UTC. At this time, southwesterly valley winds prevail in the valley, while southerly winds occur above. This finding highlights the height-dependent advection of ozone due to interacting mesoscale circulation systems. These dynamical processes need to be represented adequately in CTMs to deliver a realistic description of the ozone concentration fields.

Halogen and Sulfur Reactions Relevant to Polar Chemistry

NASA Technical Reports Server (NTRS)

Wine, Paul H.; Nicovich, J. Michael; Stickel, Robert E.; Zhao, Z.; Shackleford, C. J.; Kreutter, K. D.; Daykin, E. P.; Wang, S.

1997-01-01

It is widely hypothesized that catalytic cycles involving BrO(x) species play an important role in the episodic destruction of ground-level ozone which is observed in the springtime Arctic boundary layer, although the exact mechanism for production of BrO(x) radicals remains an open question [Barrie et al., Bottenheim et al.; Finlayson-Pitts et al., McConnell et al.] The critical evidence linking ozone depletion with BrO(x) chemistry is an observed negative correlation between ozone and filterable bromine [Bottenheim et al., Kieser et al.] In a recent field study of springtime Arctic boundary layer chemistry [Kieser et al.] ozone concentrations and ethane concentrations were found to be correlated; this observation suggests chlorine atoms (which react rapidly with ethane) may also be an important catalyst for ozone destruction under springtime Arctic conditions.

Interrelation of changes in the total content of ozone in the northern hemisphere with the velocity of the stratosphere circumpolar vortex

NASA Astrophysics Data System (ADS)

Kolyada, Maria N.; Kashkin, Valentin B.

2004-12-01

Considering the high significance of the ozone for preservation and maintenance of the biosphere and the temperature balance of the atmosphere the investigation of the ozone layer is a very important part of the investigation of the planet"s atmosphere. In this work results of investigations of TOC variability in the Northern Hemisphere and the influence of variability of the circumpolar vortex rotation velocity on the ozone layer are presented. Mean values of total ozone concentration in the Northern Hemisphere (by satellite data) and rotation velocities of the circumpolar vortex are calculated for each month from February to April during 1998-2004. Also in this work the mechanism of the influence of the natural factors on TOC variability solar activity during the spring is suggested.

40 CFR 52.977 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control strategy and regulations: Ozone... and regulations: Ozone. (a) Determination of Attainment. Effective March 12, 2010 EPA has determined the Baton Rouge 1-hour ozone nonattainment area has attained the 1-hour ozone National Ambient Air...

40 CFR 52.2332 - Control Strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 5 2014-07-01 2014-07-01 false Control Strategy: Ozone. 52.2332...: Ozone. Determinations—EPA is determining that, as of July 18, 1995, the Salt Lake and Davis Counties ozone nonattainment area has attained the ozone standard based on air quality monitoring data from 1992...

40 CFR 52.977 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control strategy and regulations: Ozone... and regulations: Ozone. (a) Determination of Attainment. Effective March 12, 2010 EPA has determined the Baton Rouge 1-hour ozone nonattainment area has attained the 1-hour ozone National Ambient Air...

40 CFR 52.977 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy and regulations: Ozone... and regulations: Ozone. (a) Determination of Attainment. Effective March 12, 2010 EPA has determined the Baton Rouge 1-hour ozone nonattainment area has attained the 1-hour ozone National Ambient Air...

40 CFR 52.2037 - Control strategy plans for attainment and rate-of-progress: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... and rate-of-progress: Ozone. 52.2037 Section 52.2037 Protection of Environment ENVIRONMENTAL... (CONTINUED) Pennsylvania § 52.2037 Control strategy plans for attainment and rate-of-progress: Ozone. (a... ozone nonattainment area has attained the ozone standard and that the reasonable further progress and...

40 CFR 52.977 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control strategy and regulations: Ozone... and regulations: Ozone. Determination of Attainment. Effective March 12, 2010 EPA has determined the Baton Rouge 1-hour ozone nonattainment area has attained the 1-hour ozone National Ambient Air Quality...

40 CFR 52.282 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control strategy and regulations: Ozone... and regulations: Ozone. (a) Attainment determination. EPA has determined that the Ventura County severe 1-hour ozone nonattainment area attained the 1-hour ozone NAAQS by the applicable attainment date...

40 CFR 52.2332 - Control Strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control Strategy: Ozone. 52.2332...: Ozone. Determinations—EPA is determining that, as of July 18, 1995, the Salt Lake and Davis Counties ozone nonattainment area has attained the ozone standard based on air quality monitoring data from 1992...

40 CFR 52.282 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control strategy and regulations: Ozone... and regulations: Ozone. (a) Attainment determination. EPA has determined that the Ventura County severe 1-hour ozone nonattainment area attained the 1-hour ozone NAAQS by the applicable attainment date...

40 CFR 52.2332 - Control Strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 5 2013-07-01 2013-07-01 false Control Strategy: Ozone. 52.2332...: Ozone. Determinations—EPA is determining that, as of July 18, 1995, the Salt Lake and Davis Counties ozone nonattainment area has attained the ozone standard based on air quality monitoring data from 1992...

40 CFR 52.282 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy and regulations: Ozone... and regulations: Ozone. (a) Attainment determination. EPA has determined that the Ventura County severe 1-hour ozone nonattainment area attained the 1-hour ozone NAAQS by the applicable attainment date...

40 CFR 52.282 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control strategy and regulations: Ozone... and regulations: Ozone. (a) Attainment determination. EPA has determined that the Ventura County severe 1-hour ozone nonattainment area attained the 1-hour ozone NAAQS by the applicable attainment date...

40 CFR 52.282 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control strategy and regulations: Ozone... and regulations: Ozone. (a) Attainment determination. EPA has determined that the Ventura County severe 1-hour ozone nonattainment area attained the 1-hour ozone NAAQS by the applicable attainment date...

40 CFR 52.1342 - Control strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.1342...: Ozone. (a) Determination of attainment. EPA has determined, as of June 9, 2011, that the St. Louis (MO-IL) metropolitan 1997 8-hour ozone nonattainment area has attained the 1997 8-hour ozone NAAQS. This...

40 CFR 52.2332 - Control Strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control Strategy: Ozone. 52.2332...: Ozone. Determinations—EPA is determining that, as of July 18, 1995, the Salt Lake and Davis Counties ozone nonattainment area has attained the ozone standard based on air quality monitoring data from 1992...

40 CFR 52.1342 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.1342...: Ozone. Determination of Attainment. EPA has determined, as of June 9, 2011, that the St. Louis (MO-IL) metropolitan 1997 8-hour ozone nonattainment area has attained the 1997 8-hour ozone NAAQS. This determination...

40 CFR 52.1342 - Control strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.1342...: Ozone. (a) Determination of attainment. EPA has determined, as of June 9, 2011, that the St. Louis (MO-IL) metropolitan 1997 8-hour ozone nonattainment area has attained the 1997 8-hour ozone NAAQS. This...

40 CFR 52.977 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control strategy and regulations: Ozone... and regulations: Ozone. (a) Determination of Attainment. Effective March 12, 2010 EPA has determined the Baton Rouge 1-hour ozone nonattainment area has attained the 1-hour ozone National Ambient Air...

40 CFR 52.1342 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.1342...: Ozone. (a) Determination of attainment. EPA has determined, as of June 9, 2011, that the St. Louis (MO-IL) metropolitan 1997 8-hour ozone nonattainment area has attained the 1997 8-hour ozone NAAQS. This...

40 CFR 52.2332 - Control Strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control Strategy: Ozone. 52.2332...: Ozone. Determinations—EPA is determining that, as of July 18, 1995, the Salt Lake and Davis Counties ozone nonattainment area has attained the ozone standard based on air quality monitoring data from 1992...

A cloud-ozone data product from Aura OMI and MLS satellite measurements

NASA Astrophysics Data System (ADS)

Ziemke, Jerald R.; Strode, Sarah A.; Douglass, Anne R.; Joiner, Joanna; Vasilkov, Alexander; Oman, Luke D.; Liu, Junhua; Strahan, Susan E.; Bhartia, Pawan K.; Haffner, David P.

2017-11-01

Ozone within deep convective clouds is controlled by several factors involving photochemical reactions and transport. Gas-phase photochemical reactions and heterogeneous surface chemical reactions involving ice, water particles, and aerosols inside the clouds all contribute to the distribution and net production and loss of ozone. Ozone in clouds is also dependent on convective transport that carries low-troposphere/boundary-layer ozone and ozone precursors upward into the clouds. Characterizing ozone in thick clouds is an important step for quantifying relationships of ozone with tropospheric H2O, OH production, and cloud microphysics/transport properties. Although measuring ozone in deep convective clouds from either aircraft or balloon ozonesondes is largely impossible due to extreme meteorological conditions associated with these clouds, it is possible to estimate ozone in thick clouds using backscattered solar UV radiation measured by satellite instruments. Our study combines Aura Ozone Monitoring Instrument (OMI) and Microwave Limb Sounder (MLS) satellite measurements to generate a new research product of monthly-mean ozone concentrations in deep convective clouds between 30° S and 30° N for October 2004-April 2016. These measurements represent mean ozone concentration primarily in the upper levels of thick clouds and reveal key features of cloud ozone including: persistent low ozone concentrations in the tropical Pacific of ˜ 10 ppbv or less; concentrations of up to 60 pphv or greater over landmass regions of South America, southern Africa, Australia, and India/east Asia; connections with tropical ENSO events; and intraseasonal/Madden-Julian oscillation variability. Analysis of OMI aerosol measurements suggests a cause and effect relation between boundary-layer pollution and elevated ozone inside thick clouds over landmass regions including southern Africa and India/east Asia.

A Cloud-Ozone Data Product from Aura OMI and MLS Satellite Measurements.

PubMed

Ziemke, Jerald R; Strode, Sarah A; Douglass, Anne R; Joiner, Joanna; Vasilkov, Alexander; Oman, Luke D; Liu, Junhua; Strahan, Susan E; Bhartia, Pawan K; Haffner, David P

2017-01-01

Ozone within deep convective clouds is controlled by several factors involving photochemical reactions and transport. Gas-phase photochemical reactions and heterogeneous surface chemical reactions involving ice, water particles, and aerosols inside the clouds all contribute to the distribution and net production and loss of ozone. Ozone in clouds is also dependent on convective transport that carries low troposphere/boundary layer ozone and ozone precursors upward into the clouds. Characterizing ozone in thick clouds is an important step for quantifying relationships of ozone with tropospheric H 2 O, OH production, and cloud microphysics/transport properties. Although measuring ozone in deep convective clouds from either aircraft or balloon ozonesondes is largely impossible due to extreme meteorological conditions associated with these clouds, it is possible to estimate ozone in thick clouds using backscattered solar UV radiation measured by satellite instruments. Our study combines Aura Ozone Monitoring Instrument (OMI) and Microwave Limb Sounder (MLS) satellite measurements to generate a new research product of monthly-mean ozone concentrations in deep convective clouds between 30°S to 30°N for October 2004 - April 2016. These measurements represent mean ozone concentration primarily in the upper levels of thick clouds and reveal key features of cloud ozone including: persistent low ozone concentrations in the tropical Pacific of ~10 ppbv or less; concentrations of up to 60 pphv or greater over landmass regions of South America, southern Africa, Australia, and India/east Asia; connections with tropical ENSO events; and intra-seasonal/Madden-Julian Oscillation variability. Analysis of OMI aerosol measurements suggests a cause and effect relation between boundary layer pollution and elevated ozone inside thick clouds over land-mass regions including southern Africa and India/east Asia.

40 CFR 51.910 - What requirements for reasonable further progress (RFP) under sections 172(c)(2) and 182 apply...

Code of Federal Regulations, 2010 CFR

2010-07-01

...-hour ozone NAAQS? 51.910 Section 51.910 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.910 What... nonattainment for the 8-hour ozone NAAQS? (a) What are the general requirements for RFP for an area classified...

40 CFR 51.910 - What requirements for reasonable further progress (RFP) under sections 172(c)(2) and 182 apply...

Code of Federal Regulations, 2011 CFR

2011-07-01

...-hour ozone NAAQS? 51.910 Section 51.910 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.910 What... nonattainment for the 8-hour ozone NAAQS? (a) What are the general requirements for RFP for an area classified...

40 CFR 51.910 - What requirements for reasonable further progress (RFP) under sections 172(c)(2) and 182 apply...

Code of Federal Regulations, 2013 CFR

2013-07-01

...-hour ozone NAAQS? 51.910 Section 51.910 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.910 What... nonattainment for the 8-hour ozone NAAQS? (a) What are the general requirements for RFP for an area classified...

40 CFR 51.910 - What requirements for reasonable further progress (RFP) under sections 172(c)(2) and 182 apply...

Code of Federal Regulations, 2012 CFR

2012-07-01

...-hour ozone NAAQS? 51.910 Section 51.910 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.910 What... nonattainment for the 8-hour ozone NAAQS? (a) What are the general requirements for RFP for an area classified...

40 CFR 51.910 - What requirements for reasonable further progress (RFP) under sections 172(c)(2) and 182 apply...

Code of Federal Regulations, 2014 CFR

2014-07-01

...-hour ozone NAAQS? 51.910 Section 51.910 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.910 What... nonattainment for the 8-hour ozone NAAQS? (a) What are the general requirements for RFP for an area classified...

Ground-Based Lidar for Atmospheric Boundary Layer Ozone Measurements

NASA Technical Reports Server (NTRS)

Kuang, Shi; Newchurch, Michael J.; Burris, John; Liu, Xiong

2013-01-01

Ground-based lidars are suitable for long-term ozone monitoring as a complement to satellite and ozonesonde measurements. However, current ground-based lidars are unable to consistently measure ozone below 500 m above ground level (AGL) due to both engineering issues and high retrieval sensitivity to various measurement errors. In this paper, we present our instrument design, retrieval techniques, and preliminary results that focus on the high-temporal profiling of ozone within the atmospheric boundary layer (ABL) achieved by the addition of an inexpensive and compact mini-receiver to the previous system. For the first time, to the best of our knowledge, the lowest, consistently achievable observation height has been extended down to 125 m AGL for a ground-based ozone lidar system. Both the analysis and preliminary measurements demonstrate that this lidar measures ozone with a precision generally better than 10% at a temporal resolution of 10 min and a vertical resolution from 150 m at the bottom of the ABL to 550 m at the top. A measurement example from summertime shows that inhomogeneous ozone aloft was affected by both surface emissions and the evolution of ABL structures.

Surface ozone measurements in the southwest of the Iberian Peninsula (Huelva, Spain).

PubMed

Carnero, Jose A Adame; Bolívar, Juan P; de la Morena, Benito A

2010-02-01

Photochemical ozone pollution of the lower troposphere (LT) is a very complex process involving meteorological, topographic emissions and chemical parameters. Ozone is considered the most important air pollutant in rural, suburban and industrial areas of many sites in the world since it strongly affects human health, vegetation and forest ecosystems, and its increase during the last decades has been significant. In addition, ozone is a greenhouse gas that contributes to climate change. For these reasons, it is necessary to carry out investigations that determine the behaviour of ozone at different locations. The aim of this work is to understand the levels and temporal variations of surface ozone in an industrial-urban region of the Southwest Iberian Peninsula. The study is based on ozone hourly data recorded during a 6-year period, 2000 to 2005 at four stations and meteorological data from a coastal station. The stations used were El Arenosillo and Cartaya--both coastal stations, Huelva--an urban site and Valverde--an inland station 50 km away from the coastline. The general characteristics of the ozone series, seasonal and daily ozone cycles as well as number of exceedances of the threshold established in the European Ozone Directive have been calculated and analysed. Analysis of the meteorological data shows that winter-autumn seasons are governed by the movement of synoptic weather systems; however, in the spring-summer seasons, both synoptic and mesoescale conditions exist. Average hourly ozone concentrations range from 78.5 +/- 0.1 microg m(-3) at Valverde to 57.8 +/- 0.2 microg m(-3) at Huelva. Ozone concentrations present a seasonal variability with higher values in summer months, while in wintertime, lower values are recorded. A seasonal daily evolution has also been found with minimum levels around 08:00 UTC, which occurs approximately 1-1.5 h after sunrise, whereas the maximum is reached at about 16:00 UTC. Furthermore, during summer, the maximum value at El Arenosillo and Valverde stations remains very uniformed until 20:00 UTC. These levels could be due to the photochemical production in situ and also to the horizontal and vertical ozone transport at El Arenosillo from the reservoir layers in the sea and in the case of Valverde, the horizontal transport, thanks to the marine breeze. Finally, the data have been evaluated relative to the thresholds defined in the European Ozone Directive. The threshold to protect human health has been exceeded during the spring and summer months mainly at El Arenosillo and Valverde. The vegetation threshold has also been frequently exceeded, ranging from 131 days at Cartaya up to 266 days at Valverde. The results in the seasonal and daily variations demonstrate that El Arenosillo and Valverde stations show higher ozone concentrations than Cartaya and Huelva during the spring and summer months. Under meteorological conditions characterized by land-sea breeze circulation, the daytime sea breeze transports the emissions from urban and industrial sources in the SW further inland. Under this condition, the area located downwind to the NE is affected very easily by high ozone concentrations, which is the case for the Valverde station. Nevertheless, according to this circulation model, the El Arenosillo station located at the coast SE from these sources is not directly affected by their emissions. The ozone concentrations observed at El Arenosillo can be explained by the ozone residual layer over the sea, similar to other coastal sites in the Mediterranean basin. The temporal variations of the ozone concentrations have been studied at four measurement sites in the southwest of the Iberian Peninsula. The results obtained point out that industrial and urban emissions combined with specific meteorological conditions in spring and summer cause high ozone levels which exceed the recommended threshold limits and could affect the vegetation and human health in this area. This work is the first investigation related to surface ozone in this region; therefore, the results obtained may be a useful tool to air quality managers and policy-makers to apply possible air control strategies towards a reduction of ozone exceedances and the impact on human health and vegetation. Due to the levels, variability and underlying boundary layer dynamics, it is necessary to extend this research in this geographical area with the purpose of improving the understanding of photochemical air pollution in the Western Mediterranean Basin and in the south of the Iberian Peninsula.

Biomedical consequences of ozone depletion

NASA Astrophysics Data System (ADS)

Coohill, Thomas P.

1994-07-01

It is widely agreed that a portion of the earth's protective stratospheric ozone layer is being depleted. The major effect of this ozone loss will be an increase in the amount of ultraviolet radiation (UV reaching the biosphere. This increase will be completely contained within the UVB (290nm - 320nm). It is imperative that assessments be made of the effects of this additional UVB on living organisms. This requires a detailed knowledge of the UVB photobiology of these life forms. One analytical technique to aid in the approximations is the construction of UV action spectra for such important biological end-points as human skin cancer, cataracts, immune suppression; plant photosynthesis and crop yields; and aquatic organism responses to UVB, especially the phytoplankton. Combining these action spectra with the known solar spectrum (and estimates for various ozone depletion scenarios) can give rise to a series of effectiveness spectra for these parameters. This manuscript gives a first approximation, rough estimate, for the effectiveness spectra for some of these bioresponses, and a series of crude temporary values for how a 10% ozone loss would affect the above end-points. These are not intended to masquerade as final answers, but rather, to serve as beginning attempts for a process which should be continually refined. It is hoped that these estimates will be of some limited use to agencies, such as government and industry, that have to plan now for changes in human activities that might alter future atmospheric chemistry in a beneficial manner.

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.

Atmospheric Transport and Photochemistry of Ozone Over Central Southern Africa During the Southern Africa Fire-Atmosphere Research Initiative

NASA Technical Reports Server (NTRS)

Tyson, P. D.; Garstang, M.; Thompson, A. M.; DAbreton, P.; Diab, R. D.; Browell, E. V.

1997-01-01

Vertically integrated back and forward trajectories for the 300-200, 700-500 and surface-800 hPa levels are calculated using Pretoria as point of origin for the Southern Africa Fire-Atmosphere Research Initiative (SAFARI) period September-October 1992. The transport fields are then combined to show both horizontal and vertical transport of air to and from Pretoria at the different levels. Air transport patterns in the vertical are linked to the occurrence of absolutely stable layers which are also evident in the 16 ozonesonde profiles recorded at Pretoria during SAFARI. The coherence of the stratification based on dynamical and ozone analysis permits the use of mean ozone profiles with air volume fluxes to interpret the ozone in terms of photochemistry and transport within stable layers. Extensive recirculation across the meridional plane at Pretoria implies that advection of ozone is slow and that photochemistry is responsible for the observed vertical structure over central southern Africa in September and October 1992. Requisite ozone formation rates are supported by model analysis of ozone and ozone precursors measured from SAFARI and Transport and Atmospheric Research Chemistry near the Equator-Atlantic aircraft.

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…

Stable ozone layer in Norway and USSR

NASA Technical Reports Server (NTRS)

Henriksen, K.; Svenoe, T.; Terez, E. I.; Terez, G. A.; Roldugin, V.; Larsen, S. H. H.

1994-01-01

Long-term column ozone density measurements have been carried out in Norway and USSR. Data from Tromso and two meridional chains in USSR are analyzed, and most of the stations show that no significant decreasing trend in ozone has occurred during the last two decades.

40 CFR 97.521 - Recordation of TR NOX Ozone Season allowance allocations and auction results.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Recordation of TR NOX Ozone Season... SO2 TRADING PROGRAMS TR NOX Ozone Season Trading Program § 97.521 Recordation of TR NOX Ozone Season... Ozone Season source's compliance account the TR NOX Ozone Season allowances allocated to the TR NOX...

40 CFR 97.521 - Recordation of TR NOX Ozone Season allowance allocations and auction results.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Recordation of TR NOX Ozone Season... SO2 TRADING PROGRAMS TR NOX Ozone Season Trading Program § 97.521 Recordation of TR NOX Ozone Season... Ozone Season source's compliance account the TR NOX Ozone Season allowances allocated to the TR NOX...

40 CFR 97.521 - Recordation of TR NOX Ozone Season allowance allocations and auction results.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Recordation of TR NOX Ozone Season... SO2 TRADING PROGRAMS TR NOX Ozone Season Trading Program § 97.521 Recordation of TR NOX Ozone Season... Ozone Season source's compliance account the TR NOX Ozone Season allowances allocated to the TR NOX...

Airliner cabin ozone: An updated review. Final report

DOE Office of Scientific and Technical Information (OSTI.GOV)

Melton, C.E.

1989-12-01

The recent literature pertaining to ozone contamination of airliner cabins is reviewed. Measurements in airliner cabins without filters showed that ozone levels were about 50 percent of atmospheric ozone. Filters were about 90 percent effective in destroying ozone. Ozone (0.12 to 0.14 ppmv) caused mild subjective respiratory irritation in exercising men, but 0.20 to 0.30 ppmv did not have adverse effects on patients with chronic heart or lung disease. Ozone (1.0 to 2.0 ppmv) decreased survival time of influenza-infected rats and mice and suppressed the capacity of lung macrophages to destroy Listeria. Airway responses to ozone are divided into anmore » early parasympathetically mediated bronchoconstrictive phase and a later histamine-mediated congestive phase. Evidence indicates that intracellular free radicals are responsible for ozone damage and that the damage may be spread to other cells by toxic intermediate products: Antioxidants provide some protection to cells in vitro from ozone but dietary intake of antioxidant vitamins by humans has only a weak effect, if any. This review indicates that earlier findings regarding ozone toxicity do not need to be corrected. Compliance with existing FAA ozone standards appears to provide adequate protection to aircrews and passengers.« less

Long-term Measurements of Summer-time Ozone at the Walnut Grove Tower - Understanding Trends in the Boundary Layer

NASA Astrophysics Data System (ADS)

Mahmud, A.; Di, P.; Mims, D.; Avise, J.; DaMassa, J.; Kaduwela, A. P.

2015-12-01

The California Air Resources Board (CARB) has been monitoring boundary layer ozone at the Walnut Grove Tower (WGT) since 1996 for investigating regional transport and vertical profile. Walnut Grove is located between Sacramento and Stockton, CA in the Sacramento - San Joaquin Delta. Sampling inlets are positioned at 30-ft, 400-ft, 800-ft, 1200-ft and 1600-ft levels of the 2000-ft tower, which is one of the tallest monitoring towers in the Western US. Ozone, ambient temperature, wind speed, and wind direction are simultaneously measured at each level, and reported as hourly averages. The current study included analyses of available ozone and corresponding meteorological data for the months of June - September from 1996 - 2014 with objectives to: 1) explore trends and inter-annual variability of ozone, 2) examine any correlations between ozone and meteorological parameters, 3) understand interactions of ozone measured at various levels, and 4) assess how well a regulatory state-of-the-science air quality model such as the Community Multi-scale Air Quality Model (CMAQ) captures observation. Daily 1-hr maximum ozone has been consistently decreasing during the 1996 - 2014 period at a rate of ~1 ppb per year. This indicates that CARB's measures to control ambient ozone have been effective over the past years. Evolution of the vertical profile throughout the day shows that ozone is fairly homogeneously mixed between 1 - 5 pm, when mixing height typically reaches the maximum. Ozone at 30-ft shows the greatest variability because of its proximity to the ground and emissions sources - rises faster during morning hours (7 - 10 am) and declines more rapidly during evening hours (7 - 10 pm) compared to other levels. Air masses reaching the tower are predominantly southwesterly (247 - 257 deg.) at the bottom, and southwesterly to slightly northwesterly (254 - 302 deg.) at top levels. Daily 1-hr maximum ozone was negatively correlated with wind speed (i.e. ozone was high under low wind condition) and positively correlated with ambient temperature (i.e. ozone was high under high temperature condition) during ~40% and ~50% of the time, respectively. A modeling exercise for Jun - Sep of 2012 shows that CMAQ captures the observed evolution and vertical mixing of ozone throughout the day quite well in the boundary layer.

Students' Misconceptions about the Ozone Layer and the Effect of Internet-Based Media on It

ERIC Educational Resources Information Center

Gungordu, Nahide; Yalcin-Celik, Ayse; Kilic, Ziya

2017-01-01

In this study, students' misconceptions about the ozone layer were investigated, looking specifically at the effect internet-based media has on the formation of these misconceptions. Quantitative and qualitative research approaches were used to perform the research. As part of the quantitative portion of the research, the descriptive survey…

40 CFR 97.524 - Compliance with TR NOX Ozone Season emissions limitation.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Compliance with TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.524 Compliance with TR NOX Ozone Season emissions limitation. (a) Availability for deduction for compliance. TR NOX Ozone Season allowances are available to be...

40 CFR 97.360 - Submission of CAIR NOX Ozone Season allowance transfers.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Submission of CAIR NOX Ozone Season... CAIR NOX Ozone Season Allowance Transfers § 97.360 Submission of CAIR NOX Ozone Season allowance transfers. A CAIR authorized account representative seeking recordation of a CAIR NOX Ozone Season allowance...

40 CFR 97.524 - Compliance with TR NOX Ozone Season emissions limitation.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Compliance with TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.524 Compliance with TR NOX Ozone Season emissions limitation. (a) Availability for deduction for compliance. TR NOX Ozone Season allowances are available to be...

40 CFR 97.522 - Submission of TR NOX Ozone Season allowance transfers.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Submission of TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.522 Submission of TR NOX Ozone Season allowance transfers. (a) An authorized account representative seeking recordation of a TR NOX Ozone Season allowance...

40 CFR 52.1683 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.1683...: Ozone. (a) The State of New York has certified to the satisfaction of the EPA that no sources are... ozone nonattainment areas in New York listed below have attained the 1-hour ozone standard on the date...

40 CFR 97.342 - CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false CAIR NOX Ozone Season allowance... Ozone Season Allowance Allocations § 97.342 CAIR NOX Ozone Season allowance allocations. (a)(1) The baseline heat input (in mmBtu) used with respect to CAIR NOX Ozone Season allowance allocations under...

40 CFR 97.342 - CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false CAIR NOX Ozone Season allowance... Ozone Season Allowance Allocations § 97.342 CAIR NOX Ozone Season allowance allocations. (a)(1) The baseline heat input (in mmBtu) used with respect to CAIR NOX Ozone Season allowance allocations under...

40 CFR 96.342 - CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false CAIR NOX Ozone Season allowance... IMPLEMENTATION PLANS CAIR NOX Ozone Season Allowance Allocations § 96.342 CAIR NOX Ozone Season allowance allocations. (a)(1) The baseline heat input (in mmBtu) used with respect to CAIR NOX Ozone Season allowance...

40 CFR 97.341 - Timing requirements for CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Timing requirements for CAIR NOX Ozone... TRADING PROGRAMS CAIR NOX Ozone Season Allowance Allocations § 97.341 Timing requirements for CAIR NOX Ozone Season allowance allocations. (a) The Administrator will determine by order the CAIR NOX Ozone...

40 CFR 97.341 - Timing requirements for CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Timing requirements for CAIR NOX Ozone... TRADING PROGRAMS CAIR NOX Ozone Season Allowance Allocations § 97.341 Timing requirements for CAIR NOX Ozone Season allowance allocations. (a) The Administrator will determine by order the CAIR NOX Ozone...

40 CFR 97.525 - Compliance with TR NOX Ozone Season assurance provisions.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Compliance with TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.525 Compliance with TR NOX Ozone Season assurance provisions. (a) Availability for deduction. TR NOX Ozone Season allowances are available to be deducted for...

40 CFR 97.523 - Recordation of TR NOX Ozone Season allowance transfers.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Recordation of TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.523 Recordation of TR NOX Ozone Season allowance transfers... NOX Ozone Season allowance transfer that is correctly submitted under § 97.522, the Administrator will...

40 CFR 96.342 - CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false CAIR NOX Ozone Season allowance... IMPLEMENTATION PLANS CAIR NOX Ozone Season Allowance Allocations § 96.342 CAIR NOX Ozone Season allowance allocations. (a)(1) The baseline heat input (in mmBtu) used with respect to CAIR NOX Ozone Season allowance...

40 CFR 97.360 - Submission of CAIR NOX Ozone Season allowance transfers.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Submission of CAIR NOX Ozone Season... CAIR NOX Ozone Season Allowance Transfers § 97.360 Submission of CAIR NOX Ozone Season allowance transfers. A CAIR authorized account representative seeking recordation of a CAIR NOX Ozone Season allowance...

40 CFR 97.342 - CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false CAIR NOX Ozone Season allowance... Ozone Season Allowance Allocations § 97.342 CAIR NOX Ozone Season allowance allocations. (a)(1) The baseline heat input (in mmBtu) used with respect to CAIR NOX Ozone Season allowance allocations under...

40 CFR 52.1683 - Control strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.1683...: Ozone. (a) The State of New York has certified to the satisfaction of the EPA that no sources are... ozone nonattainment areas in New York listed below have attained the 1-hour ozone standard on the date...

40 CFR 97.341 - Timing requirements for CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false Timing requirements for CAIR NOX Ozone... TRADING PROGRAMS CAIR NOX Ozone Season Allowance Allocations § 97.341 Timing requirements for CAIR NOX Ozone Season allowance allocations. (a) The Administrator will determine by order the CAIR NOX Ozone...

40 CFR 97.341 - Timing requirements for CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Timing requirements for CAIR NOX Ozone... TRADING PROGRAMS CAIR NOX Ozone Season Allowance Allocations § 97.341 Timing requirements for CAIR NOX Ozone Season allowance allocations. (a) The Administrator will determine by order the CAIR NOX Ozone...

40 CFR 96.342 - CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false CAIR NOX Ozone Season allowance... IMPLEMENTATION PLANS CAIR NOX Ozone Season Allowance Allocations § 96.342 CAIR NOX Ozone Season allowance allocations. (a)(1) The baseline heat input (in mmBtu) used with respect to CAIR NOX Ozone Season allowance...

40 CFR 52.1683 - Control strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.1683...: Ozone. (a) The State of New York has certified to the satisfaction of the EPA that no sources are... that the 1-hour ozone nonattainment areas in New York listed below have attained the 1-hour ozone...

40 CFR 97.522 - Submission of TR NOX Ozone Season allowance transfers.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Submission of TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.522 Submission of TR NOX Ozone Season allowance transfers. (a) An authorized account representative seeking recordation of a TR NOX Ozone Season allowance...

40 CFR 96.342 - CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false CAIR NOX Ozone Season allowance... IMPLEMENTATION PLANS CAIR NOX Ozone Season Allowance Allocations § 96.342 CAIR NOX Ozone Season allowance allocations. (a)(1) The baseline heat input (in mmBtu) used with respect to CAIR NOX Ozone Season allowance...

40 CFR 97.522 - Submission of TR NOX Ozone Season allowance transfers.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Submission of TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.522 Submission of TR NOX Ozone Season allowance transfers. (a) An authorized account representative seeking recordation of a TR NOX Ozone Season allowance...

40 CFR 97.360 - Submission of CAIR NOX Ozone Season allowance transfers.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Submission of CAIR NOX Ozone Season... CAIR NOX Ozone Season Allowance Transfers § 97.360 Submission of CAIR NOX Ozone Season allowance transfers. A CAIR authorized account representative seeking recordation of a CAIR NOX Ozone Season allowance...

40 CFR 96.342 - CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false CAIR NOX Ozone Season allowance... IMPLEMENTATION PLANS CAIR NOX Ozone Season Allowance Allocations § 96.342 CAIR NOX Ozone Season allowance allocations. (a)(1) The baseline heat input (in mmBtu) used with respect to CAIR NOX Ozone Season allowance...

40 CFR 97.360 - Submission of CAIR NOX Ozone Season allowance transfers.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Submission of CAIR NOX Ozone Season... CAIR NOX Ozone Season Allowance Transfers § 97.360 Submission of CAIR NOX Ozone Season allowance transfers. A CAIR authorized account representative seeking recordation of a CAIR NOX Ozone Season allowance...

40 CFR 97.341 - Timing requirements for CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Timing requirements for CAIR NOX Ozone... TRADING PROGRAMS CAIR NOX Ozone Season Allowance Allocations § 97.341 Timing requirements for CAIR NOX Ozone Season allowance allocations. (a) The Administrator will determine by order the CAIR NOX Ozone...

40 CFR 97.523 - Recordation of TR NOX Ozone Season allowance transfers.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Recordation of TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.523 Recordation of TR NOX Ozone Season allowance transfers... NOX Ozone Season allowance transfer that is correctly submitted under § 97.522, the Administrator will...

40 CFR 97.342 - CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false CAIR NOX Ozone Season allowance... Ozone Season Allowance Allocations § 97.342 CAIR NOX Ozone Season allowance allocations. (a)(1) The baseline heat input (in mmBtu) used with respect to CAIR NOX Ozone Season allowance allocations under...

40 CFR 97.524 - Compliance with TR NOX Ozone Season emissions limitation.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Compliance with TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.524 Compliance with TR NOX Ozone Season emissions limitation. (a) Availability for deduction for compliance. TR NOX Ozone Season allowances are available to be...

40 CFR 97.360 - Submission of CAIR NOX Ozone Season allowance transfers.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false Submission of CAIR NOX Ozone Season... CAIR NOX Ozone Season Allowance Transfers § 97.360 Submission of CAIR NOX Ozone Season allowance transfers. A CAIR authorized account representative seeking recordation of a CAIR NOX Ozone Season allowance...

40 CFR 97.523 - Recordation of TR NOX Ozone Season allowance transfers.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Recordation of TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.523 Recordation of TR NOX Ozone Season allowance transfers... NOX Ozone Season allowance transfer that is correctly submitted under § 97.522, the Administrator will...

40 CFR 97.525 - Compliance with TR NOX Ozone Season assurance provisions.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Compliance with TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.525 Compliance with TR NOX Ozone Season assurance provisions. (a) Availability for deduction. TR NOX Ozone Season allowances are available to be deducted for...

40 CFR 52.1683 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.1683...: Ozone. (a) The State of New York has certified to the satisfaction of the EPA that no sources are... ozone nonattainment areas in New York listed below have attained the 1-hour ozone standard on the date...

40 CFR 97.342 - CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false CAIR NOX Ozone Season allowance... Ozone Season Allowance Allocations § 97.342 CAIR NOX Ozone Season allowance allocations. (a)(1) The baseline heat input (in mmBtu) used with respect to CAIR NOX Ozone Season allowance allocations under...

40 CFR 97.525 - Compliance with TR NOX Ozone Season assurance provisions.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Compliance with TR NOX Ozone Season... TR NOX Ozone Season Trading Program § 97.525 Compliance with TR NOX Ozone Season assurance provisions. (a) Availability for deduction. TR NOX Ozone Season allowances are available to be deducted for...

Photosynthetic behavior of woody species under high ozone exposure probed with the JIP-test: a review.

PubMed

Bussotti, Filippo; Strasser, Reto J; Schaub, Marcus

2007-06-01

Visible ozone symptoms on leaves are expressions of physiological mechanisms to cope with oxidative stresses. Often, the symptoms consist of stippling, which corresponds to localized cell death (hypersensitive response, HR), separated from healthy cells by a layer of callose. The HR strategy tends to protect the healthy cells and in most cases the efficiency of chlorophyll to trap energy is not affected. In other cases, the efficiency of leaves to produce biomass declines and the plant loses its photosynthetic apparatus replacing it with a new, more efficient one. Another strategy consists of the production of pigments (anthocyanins), and leaves become reddish. In these cases, the most significant physiological manifestation consists of the enhanced dissipation of energy. These different behavior patterns are reflected in the initial events of photosynthetic activity, and can be monitored with techniques based on the direct fluorescence of chlorophyll a in photosystem II, applying the JIP-test.

Effect of ozone oxidative preconditioning in preventing early radiation-induced lung injury in rats

PubMed Central

Bakkal, B.H.; Gultekin, F.A.; Guven, B.; Turkcu, U.O.; Bektas, S.; Can, M.

2013-01-01

Ionizing radiation causes its biological effects mainly through oxidative damage induced by reactive oxygen species. Previous studies showed that ozone oxidative preconditioning attenuated pathophysiological events mediated by reactive oxygen species. As inhalation of ozone induces lung injury, the aim of this study was to examine whether ozone oxidative preconditioning potentiates or attenuates the effects of irradiation on the lung. Rats were subjected to total body irradiation, with or without treatment with ozone oxidative preconditioning (0.72 mg/kg). Serum proinflammatory cytokine levels, oxidative damage markers, and histopathological analysis were compared at 6 and 72 h after total body irradiation. Irradiation significantly increased lung malondialdehyde levels as an end-product of lipoperoxidation. Irradiation also significantly decreased lung superoxide dismutase activity, which is an indicator of the generation of oxidative stress and an early protective response to oxidative damage. Ozone oxidative preconditioning plus irradiation significantly decreased malondialdehyde levels and increased the activity of superoxide dismutase, which might indicate protection of the lung from radiation-induced lung injury. Serum tumor necrosis factor alpha and interleukin-1 beta levels, which increased significantly following total body irradiation, were decreased with ozone oxidative preconditioning. Moreover, ozone oxidative preconditioning was able to ameliorate radiation-induced lung injury assessed by histopathological evaluation. In conclusion, ozone oxidative preconditioning, repeated low-dose intraperitoneal administration of ozone, did not exacerbate radiation-induced lung injury, and, on the contrary, it provided protection against radiation-induced lung damage. PMID:23969972

Ozone depletion - Ultraviolet radiation and phytoplankton biology in Antarctic waters

NASA Technical Reports Server (NTRS)

Smith, R. C.; Prezelin, B. B.; Baker, K. S.; Bidigare, R. R.; Boucher, N. P.; Coley, T.; Karentz, D.; Macintyre, S.; Matlick, H. A.; Menzies, D.

1992-01-01

The near-50-percent thinning of the stratospheric ozone layer over the Antarctic, with increased passage of mid-UV radiation to the surface of the Southern Ocean, has prompted concern over possible radiation damage to the near-surface phytoplankton communities that are the bases of Antarctic marine ecosystems. As the ozone layer thinned, a 6-week study of the marginal ice zone of the Bellingshousen Sea in the austral spring of 1990 noted sea-surface and depth-dependent ratios of mid-UV irradiance to total irradiance increased, and mid-UV inhibition of photosynthesis increased. A 6-12 percent reduction in primary production associated with ozone depletion was estimated to have occurred over the course of the present study.

40 CFR 82.1 - Purpose and scope.

Code of Federal Regulations, 2011 CFR

2011-07-01

... STRATOSPHERIC OZONE Production and Consumption Controls § 82.1 Purpose and scope. (a) The purpose of the regulations in this subpart is to implement the Montreal Protocol on Substances that Deplete the Ozone Layer... ozone-depleting substances, according to specified schedules. The Protocol also requires each nation...

40 CFR 82.1 - Purpose and scope.

Code of Federal Regulations, 2010 CFR

2010-07-01

... STRATOSPHERIC OZONE Production and Consumption Controls § 82.1 Purpose and scope. (a) The purpose of the regulations in this subpart is to implement the Montreal Protocol on Substances that Deplete the Ozone Layer... ozone-depleting substances, according to specified schedules. The Protocol also requires each nation...

40 CFR 82.1 - Purpose and scope.

Code of Federal Regulations, 2013 CFR

2013-07-01

... STRATOSPHERIC OZONE Production and Consumption Controls § 82.1 Purpose and scope. (a) The purpose of the regulations in this subpart is to implement the Montreal Protocol on Substances that Deplete the Ozone Layer... ozone-depleting substances, according to specified schedules. The Protocol also requires each nation...

40 CFR 82.1 - Purpose and scope.

Code of Federal Regulations, 2014 CFR

2014-07-01

... STRATOSPHERIC OZONE Production and Consumption Controls § 82.1 Purpose and scope. (a) The purpose of the regulations in this subpart is to implement the Montreal Protocol on Substances that Deplete the Ozone Layer... ozone-depleting substances, according to specified schedules. The Protocol also requires each nation...

40 CFR 82.1 - Purpose and scope.

Code of Federal Regulations, 2012 CFR

2012-07-01

... STRATOSPHERIC OZONE Production and Consumption Controls § 82.1 Purpose and scope. (a) The purpose of the regulations in this subpart is to implement the Montreal Protocol on Substances that Deplete the Ozone Layer... ozone-depleting substances, according to specified schedules. The Protocol also requires each nation...

Ozone (Environmental Health Student Portal)

MedlinePlus

... Environmental Protection Agency) - Describes ozone depletion effects on human health, plants, marine ecosystems, and biogeochemical cycles. Ozone (Tox ... Medicine National Institutes of Health U.S. Department of Health and Human Services

Ozone Enhancement in the Lower Troposphere over East Asia Observed by OMI: Evidence of Transboundary Pollution Transport from China to Korea and Japan

NASA Astrophysics Data System (ADS)

Hayashida, S.; Ono, A.; Liu, X.; Yang, K.; Kanaya, Y.; Chance, K.

2014-12-01

Liu et al. (2010) developed an algorithm to retrieve ozone profiles from the ground to ~60 km from OMI ultraviolet radiances using the optimal estimation technique (Rogers, 2000). This algorithm is for derivation of an ozone profile divided into 24 layers, with three layers in the troposphere (0-3km, 3-6km, 6-9km). In this study, we report results for the analysis of lower tropospheric ozone over CEC using the OMI ozone profiles mentioned above. First, we show good correlation of OMI-derived ozone with aircraft measurements and ozonesonde measurements. Second, we show significant enhancement of ozone derived from OMI over CEC. To interpret this remarkable enhancement of ozone, we show correlation of ozone with carbon monoxide (CO) and hotspot numbers suggesting the effects of crop burning on ozone enhancement. Third, we also show complementary data obtained in the field campaign at Mt. Tai in 2005 and 2006 (Kayana et al., 2013) to demonstrate ozone enhancement in June every year and show the relationship with residue burning in fields over Shandong and Hebei Provinces. Finally, we show important evidence of transboundary pollution transport from China to Korea and Japan.References:Kanaya, Y., et al. (2013), Atmos. Chem. Phys., 13(16), 8265-8283.Liu, X., et al. (2010), Atmos. Chem. Phys., 10(5), 2521-2537.Rodgers, C. D. (2000), Inverse methods for atmospheric sounding: Theory and practice, World Scientific Publishing, Singapore.

Atomic layer deposition of dielectrics on graphene using reversibly physisorbed ozone.

PubMed

Jandhyala, Srikar; Mordi, Greg; Lee, Bongki; Lee, Geunsik; Floresca, Carlo; Cha, Pil-Ryung; Ahn, Jinho; Wallace, Robert M; Chabal, Yves J; Kim, Moon J; Colombo, Luigi; Cho, Kyeongjae; Kim, Jiyoung

2012-03-27

Integration of graphene field-effect transistors (GFETs) requires the ability to grow or deposit high-quality, ultrathin dielectric insulators on graphene to modulate the channel potential. Here, we study a novel and facile approach based on atomic layer deposition through ozone functionalization to deposit high-κ dielectrics (such as Al(2)O(3)) without breaking vacuum. The underlying mechanisms of functionalization have been studied theoretically using ab initio calculations and experimentally using in situ monitoring of transport properties. It is found that ozone molecules are physisorbed on the surface of graphene, which act as nucleation sites for dielectric deposition. The physisorbed ozone molecules eventually react with the metal precursor, trimethylaluminum to form Al(2)O(3). Additionally, we successfully demonstrate the performance of dual-gated GFETs with Al(2)O(3) of sub-5 nm physical thickness as a gate dielectric. Back-gated GFETs with mobilities of ~19,000 cm(2)/(V·s) are also achieved after Al(2)O(3) deposition. These results indicate that ozone functionalization is a promising pathway to achieve scaled gate dielectrics on graphene without leaving a residual nucleation layer. © 2012 American Chemical Society

Estimation of NOx Production from Terrestrial Gamma-ray Flashes

NASA Astrophysics Data System (ADS)

Cramer, E. S.; Briggs, M. S.; Liu, N.; Mailyan, B.; Rassoul, H.; Dwyer, J. R.

2016-12-01

The motivation of this work is to understand the effects of TGFs on the ozone layer. One of the main ozone-destroying mechanisms is the production of NOx in the stratospheric region. We first review the mechanisms for NOx production in this region, specifically looking at the global rate produced by lightning. Terrestrial Gamma-ray Flashes, with runaway electron avalanches and the subsequent bremsstrahlung gamma rays, produce atmospheric ionization at all altitudes of the atmosphere. TGFs might have a greater impact on the ozone concentration in the stratosphere since they directly produce ionization and thus NOx in the ozone layer. In order to study the effect from TGFs, we use the runaway electron avalanche model (REAM) to simulate a typical TGF. The photons are then transported through Earth's atmosphere, where they deposit some of their energy as ionization in the ozone layer. We then calculate the number of NOx molecules produced by considering the average energy required to produce one electron-ion pair (W = 35 eV). The W factor has been experimentally quantified and is constant for various types of radiation and over large energy ranges and electric fields. Finally, the effect of TGF NOx production is estimated using the global annual rate of TGFs.

OZONE OVER SAN FRANCISCO. MEANS AND PATTERNS DURING POLLUTION EPISODES

EPA Science Inventory

Measurements of meteorological parameters were taken at six levels and ozone at four levels between 260m and 473m ASL on the Mt. Sutro T.V. Tower in San Francisco during the summers of 1974 through 1976. Hourly average ozone concentrations within the elevated inversion layer at t...

Polar boundary layer bromine explosion and ozone depletion events in the chemistry-climate model EMAC v2.52: implementation and evaluation of AirSnow algorithm

NASA Astrophysics Data System (ADS)

Falk, Stefanie; Sinnhuber, Björn-Martin

2018-03-01

Ozone depletion events (ODEs) in the polar boundary layer have been observed frequently during springtime. They are related to events of boundary layer enhancement of bromine. Consequently, increased amounts of boundary layer volume mixing ratio (VMR) and vertical column densities (VCDs) of BrO have been observed by in situ observation, ground-based as well as airborne remote sensing, and from satellites. These so-called bromine explosion (BE) events have been discussed serving as a source of tropospheric BrO at high latitudes, which has been underestimated in global models so far. We have implemented a treatment of bromine release and recycling on sea-ice- and snow-covered surfaces in the global chemistry-climate model EMAC (ECHAM/MESSy Atmospheric Chemistry) based on the scheme of Toyota et al. (2011). In this scheme, dry deposition fluxes of HBr, HOBr, and BrNO3 over ice- and snow-covered surfaces are recycled into Br2 fluxes. In addition, dry deposition of O3, dependent on temperature and sunlight, triggers a Br2 release from surfaces associated with first-year sea ice. Many aspects of observed bromine enhancements and associated episodes of near-complete depletion of boundary layer ozone, both in the Arctic and in the Antarctic, are reproduced by this relatively simple approach. We present first results from our global model studies extending over a full annual cycle, including comparisons with Global Ozone Monitoring Experiment (GOME) satellite BrO VCDs and surface ozone observations.

40 CFR 96.386 - Withdrawal from CAIR NOX Ozone Season Trading Program.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Withdrawal from CAIR NOX Ozone Season... STATE IMPLEMENTATION PLANS CAIR NOX Ozone Season Opt-in Units § 96.386 Withdrawal from CAIR NOX Ozone Season Trading Program. Except as provided under paragraph (g) of this section, a CAIR NOX Ozone Season...

40 CFR 97.386 - Withdrawal from CAIR NOX Ozone Season Trading Program.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Withdrawal from CAIR NOX Ozone Season... CAIR NOX Ozone Season Opt-in Units § 97.386 Withdrawal from CAIR NOX Ozone Season Trading Program. Except as provided under paragraph (g) of this section, a CAIR NOX Ozone Season opt-in unit may withdraw...

40 CFR 97.353 - Recordation of CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Recordation of CAIR NOX Ozone Season... CAIR NOX Ozone Season Allowance Tracking System § 97.353 Recordation of CAIR NOX Ozone Season allowance allocations. (a) By September 30, 2007, the Administrator will record in the CAIR NOX Ozone Season sources...

40 CFR 97.386 - Withdrawal from CAIR NOX Ozone Season Trading Program.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false Withdrawal from CAIR NOX Ozone Season... CAIR NOX Ozone Season Opt-in Units § 97.386 Withdrawal from CAIR NOX Ozone Season Trading Program. Except as provided under paragraph (g) of this section, a CAIR NOX Ozone Season opt-in unit may withdraw...

40 CFR 96.386 - Withdrawal from CAIR NOX Ozone Season Trading Program.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Withdrawal from CAIR NOX Ozone Season... STATE IMPLEMENTATION PLANS CAIR NOX Ozone Season Opt-in Units § 96.386 Withdrawal from CAIR NOX Ozone Season Trading Program. Except as provided under paragraph (g) of this section, a CAIR NOX Ozone Season...

40 CFR 97.386 - Withdrawal from CAIR NOX Ozone Season Trading Program.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Withdrawal from CAIR NOX Ozone Season... CAIR NOX Ozone Season Opt-in Units § 97.386 Withdrawal from CAIR NOX Ozone Season Trading Program. Except as provided under paragraph (g) of this section, a CAIR NOX Ozone Season opt-in unit may withdraw...

40 CFR 96.386 - Withdrawal from CAIR NOX Ozone Season Trading Program.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Withdrawal from CAIR NOX Ozone Season... STATE IMPLEMENTATION PLANS CAIR NOX Ozone Season Opt-in Units § 96.386 Withdrawal from CAIR NOX Ozone Season Trading Program. Except as provided under paragraph (g) of this section, a CAIR NOX Ozone Season...

40 CFR 97.386 - Withdrawal from CAIR NOX Ozone Season Trading Program.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Withdrawal from CAIR NOX Ozone Season... CAIR NOX Ozone Season Opt-in Units § 97.386 Withdrawal from CAIR NOX Ozone Season Trading Program. Except as provided under paragraph (g) of this section, a CAIR NOX Ozone Season opt-in unit may withdraw...

40 CFR 97.511 - Timing requirements for TR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Timing requirements for TR NOX Ozone... TRADING PROGRAMS TR NOX Ozone Season Trading Program § 97.511 Timing requirements for TR NOX Ozone Season allowance allocations. (a) Existing units. (1) TR NOX Ozone Season allowances are allocated, for the control...

40 CFR 97.353 - Recordation of CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false Recordation of CAIR NOX Ozone Season... CAIR NOX Ozone Season Allowance Tracking System § 97.353 Recordation of CAIR NOX Ozone Season allowance allocations. (a) By September 30, 2007, the Administrator will record in the CAIR NOX Ozone Season sources...

40 CFR 97.512 - TR NOX Ozone Season allowance allocations to new units.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false TR NOX Ozone Season allowance... TR NOX Ozone Season Trading Program § 97.512 TR NOX Ozone Season allowance allocations to new units. (a) For each control period in 2012 and thereafter and for the TR NOX Ozone Season units in each...

40 CFR 97.353 - Recordation of CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Recordation of CAIR NOX Ozone Season... CAIR NOX Ozone Season Allowance Tracking System § 97.353 Recordation of CAIR NOX Ozone Season allowance allocations. (a) By September 30, 2007, the Administrator will record in the CAIR NOX Ozone Season sources...

40 CFR 97.353 - Recordation of CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Recordation of CAIR NOX Ozone Season... CAIR NOX Ozone Season Allowance Tracking System § 97.353 Recordation of CAIR NOX Ozone Season allowance allocations. (a) By September 30, 2007, the Administrator will record in the CAIR NOX Ozone Season sources...

40 CFR 96.386 - Withdrawal from CAIR NOX Ozone Season Trading Program.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false Withdrawal from CAIR NOX Ozone Season... STATE IMPLEMENTATION PLANS CAIR NOX Ozone Season Opt-in Units § 96.386 Withdrawal from CAIR NOX Ozone Season Trading Program. Except as provided under paragraph (g) of this section, a CAIR NOX Ozone Season...

40 CFR 97.386 - Withdrawal from CAIR NOX Ozone Season Trading Program.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Withdrawal from CAIR NOX Ozone Season... CAIR NOX Ozone Season Opt-in Units § 97.386 Withdrawal from CAIR NOX Ozone Season Trading Program. Except as provided under paragraph (g) of this section, a CAIR NOX Ozone Season opt-in unit may withdraw...

40 CFR 97.511 - Timing requirements for TR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Timing requirements for TR NOX Ozone... TRADING PROGRAMS TR NOX Ozone Season Trading Program § 97.511 Timing requirements for TR NOX Ozone Season allowance allocations. (a) Existing units. (1) TR NOX Ozone Season allowances are allocated, for the control...

40 CFR 96.386 - Withdrawal from CAIR NOX Ozone Season Trading Program.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Withdrawal from CAIR NOX Ozone Season... STATE IMPLEMENTATION PLANS CAIR NOX Ozone Season Opt-in Units § 96.386 Withdrawal from CAIR NOX Ozone Season Trading Program. Except as provided under paragraph (g) of this section, a CAIR NOX Ozone Season...

40 CFR 97.512 - TR NOX Ozone Season allowance allocations to new units.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false TR NOX Ozone Season allowance... TR NOX Ozone Season Trading Program § 97.512 TR NOX Ozone Season allowance allocations to new units. (a) For each control period in 2012 and thereafter and for the TR NOX Ozone Season units in each...

40 CFR 97.353 - Recordation of CAIR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Recordation of CAIR NOX Ozone Season... CAIR NOX Ozone Season Allowance Tracking System § 97.353 Recordation of CAIR NOX Ozone Season allowance allocations. (a) By September 30, 2007, the Administrator will record in the CAIR NOX Ozone Season sources...

40 CFR 97.512 - TR NOX Ozone Season allowance allocations to new units.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false TR NOX Ozone Season allowance... TR NOX Ozone Season Trading Program § 97.512 TR NOX Ozone Season allowance allocations to new units. (a) For each control period in 2012 and thereafter and for the TR NOX Ozone Season units in each...

40 CFR 97.511 - Timing requirements for TR NOX Ozone Season allowance allocations.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Timing requirements for TR NOX Ozone... TRADING PROGRAMS TR NOX Ozone Season Trading Program § 97.511 Timing requirements for TR NOX Ozone Season allowance allocations. (a) Existing units. (1) TR NOX Ozone Season allowances are allocated, for the control...

Evildoer or Do-Gooder: Getting the Goods on Ozone

ERIC Educational Resources Information Center

Fisher, Diane K.

2008-01-01

This article describes the differences of good ozone and bad ozone. Good ozone, which is found in the stratosphere, protects people and other living things from the bad things UV can do, such skin cancer, cataracts, and other problems. However, lower in the atmosphere, at the top of the troposphere (around 12 miles up), ozone acts like a…

78 FR 17161 - Approval and Promulgation of Air Quality Implementation Plans; District of Columbia, Maryland and...

Federal Register 2010, 2011, 2012, 2013, 2014

2013-03-20

... 1997 ozone NAAQS which revised the health-based NAAQS for ozone by setting the NAAQS at 0.08 parts per... evidence demonstrating that ozone causes adverse health effects at lower ozone concentrations and over... determined that the 1997 ozone NAAQS would be more protective of human health, especially for children and...

Kindergarten Teachers' Conceptual Framework on the Ozone Layer Depletion. Exploring the Associative Meanings of a Global Environmental Issue

ERIC Educational Resources Information Center

Daskolia, Maria; Flogaitis, Evgenia; Papageorgiou, Evgenia

2006-01-01

This paper reports on a study conducted among Greek kindergarten teachers aiming to explore their conceptual frameworks on a major environmental issue of our times: the ozone layer depletion. The choice of this particular issue was premised on its novelty, complexity and abstractness which present teachers with difficulties in its teaching. A free…

Turkish Primary Science Teacher Candidates' Understandings of Global Warming and Ozone Layer Depletion

ERIC Educational Resources Information Center

Yalcin, Fatma Aggul; Yalcin, Mehmet

2017-01-01

The purpose of the study was to explore Turkish primary science teacher candidates' understanding of global warming and ozone layer depletion. In the study, as the research approach the survey method was used. The sample consisted of one hundred eighty nine third grade science teacher candidates. Data was collected using the tool developed by the…

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. (a...

Influence of corona discharge on the ozone budget in the tropical free troposphere: a case study of deep convection during GABRIEL

NASA Astrophysics Data System (ADS)

Bozem, H.; Fischer, H.; Gurk, C.; Schiller, C. L.; Parchatka, U.; Koenigstedt, R.; Stickler, A.; Martinez, M.; Harder, H.; Kubistin, D.; Williams, J.; Eerdekens, G.; Lelieveld, J.

2014-09-01

Convective redistribution of ozone and its precursors between the boundary layer (BL) and the free troposphere (FT) influences photochemistry, in particular in the middle and upper troposphere (UT). We present a case study of convective transport during the GABRIEL campaign over the tropical rain forest in Suriname in October 2005. During one measurement flight the inflow and outflow regions of a cumulonimbus cloud (Cb) have been characterized. We identified a distinct layer between 9 and 11 km altitude with enhanced mixing ratios of CO, O3, HOx, acetone and acetonitrile. The elevated O3 contradicts the expectation that convective transport brings low-ozone air from the boundary layer to the outflow region. Entrainment of ozone-rich air is estimated to account for 62% (range: 33-91%) of the observed O3. Ozone is enhanced by only 5-6% by photochemical production in the outflow due to enhanced NO from lightning, based on model calculations using observations including the first reported HOx measurements over the tropical rainforest. The "excess" ozone in the outflow is most probably due to direct production by corona discharge associated with lightning. We deduce a production rate of 5.12 × 1028 molecules O3 flash-1 (range: 9.89 × 1026-9.82 × 1028 molecules O3 flash-1), which is at the upper limit of the range reported previously.

Effect of UV-ozone treatment on poly(dimethylsiloxane) membranes: surface characterization and gas separation performance.

PubMed

Fu, Ywu-Jang; Qui, Hsuan-zhi; Liao, Kuo-Sung; Lue, Shingjiang Jessie; Hu, Chien-Chieh; Lee, Kueir-Rarn; Lai, Juin-Yih

2010-03-16

A thin SiO(x) selective surface layer was formed on a series of cross-linked poly(dimethylsiloxane) (PDMS) membranes by exposure to ultraviolet light at room temperature in the presence of ozone. The conversion of the cross-linked polysiloxane to SiO(x) was monitored by attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), energy-dispersive X-ray (EDX) microanalysis, contact angle analysis, and atomic force microscopy (AFM). The conversion of the cross-linked polysiloxane to SiO(x) increased with UV-ozone exposure time and cross-linking agent content, and the surface possesses highest conversion. The formation of a SiO(x) layer increased surface roughness, but it decreased water contact angle. Gas permeation measurements on the UV-ozone exposure PDMS membranes documented interesting gas separation properties: the O(2) permeability of the cross-linked PDMS membrane before UV-ozone exposure was 777 barrer, and the O(2)/N(2) selectivity was 1.9; after UV-ozone exposure, the permeability decreased to 127 barrer while the selectivity increased to 5.4. The free volume depth profile of the SiO(x) layer was investigated by novel slow positron beam. The results show that free volume size increased with the depth, yet the degree of siloxane conversion to SiO(x) does not affect the amount of free volume.

Nonessential Products Ban Program

EPA Pesticide Factsheets

Learn about EPA's efforts to address ozone layer depletion by banning the sale and introduction into interstate commerce of certain non-essential products manufactured with or containing ozone-depleting substances.

Ozone Quenching Properties of Isoprene and Its Antioxidant Role in Leaves1

PubMed Central

Loreto, Francesco; Mannozzi, Michela; Maris, Christophe; Nascetti, Pamela; Ferranti, Francesco; Pasqualini, Stefania

2001-01-01

Isoprene is formed in and emitted by plants and the reason for this apparent carbon waste is still unclear. It has been proposed that isoprene stabilizes cell and particularly chloroplast thylakoid membranes. We tested if membrane stabilization or isoprene reactivity with ozone induces protection against acute ozone exposures. The reduction of visible, physiological, anatomical, and ultrastructural (chloroplast) damage shows that clones of plants sensitive to ozone and unable to emit isoprene become resistant to acute and short exposure to ozone if they are fumigated with exogenous isoprene, and that isoprene-emitting plants that are sensitive to ozone do not suffer damage when exposed to ozone. Isoprene-induced ozone resistance is associated with the maintenance of photochemical efficiency and with a low energy dissipation, as indicated by fluorescence quenching. This suggests that isoprene effectively stabilizes thylakoid membranes. However, when isoprene reacts with ozone within the leaves or in a humid atmosphere, it quenches the ozone concentration to levels that are less or non-toxic for plants. Thus, protection from ozone in plants fumigated with isoprene may be due to a direct ozone quenching rather than to an induced resistance at membrane level. Irrespective of the mechanism, isoprene is one of the most effective antioxidants in plants. PMID:11457950

40 CFR 52.1534 - Control strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.1534... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the New Hampshire Department... revisions are for the purpose of satisfying the one-hour ozone attainment demonstration requirements of...

40 CFR 52.350 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.350 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Colorado § 52.350 Control strategy: Ozone. (a) Revisions to the Colorado State Implementation Plan, 1-hour ozone NAAQS Redesignation Request and Maintenance...

40 CFR 52.1129 - Control strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Ozone. 52.1129... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the Massachusetts Department...) and 182(c)(2)(B) of the Clean Air Act for the Springfield, Massachusetts serious ozone nonattainment...

40 CFR 52.350 - Control strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.350 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Colorado § 52.350 Control strategy: Ozone. (a) Revisions to the Colorado State Implementation Plan, 1-hour ozone NAAQS Redesignation Request and Maintenance...

40 CFR 52.1129 - Control strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.1129... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the Massachusetts Department...) and 182(c)(2)(B) of the Clean Air Act for the Springfield, Massachusetts serious ozone nonattainment...

40 CFR 52.2585 - Control strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 5 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.2585... strategy: Ozone. (a) Disapproval—On November 6, 1986, the Wisconsin Department of Natural Resources submitted as a proposed revision to the State's ozone State Implementation Plan a site-specific reasonably...

40 CFR 52.2585 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.2585... strategy: Ozone. (a) Disapproval—On November 6, 1986, the Wisconsin Department of Natural Resources submitted as a proposed revision to the State's ozone State Implementation Plan a site-specific reasonably...

40 CFR 52.350 - Control strategy: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 3 2014-07-01 2014-07-01 false Control strategy: Ozone. 52.350 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Colorado § 52.350 Control strategy: Ozone. (a) Revisions to the Colorado State Implementation Plan, 1-hour ozone NAAQS Redesignation Request and Maintenance...

40 CFR 52.1534 - Control strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Ozone. 52.1534... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the New Hampshire Department... revisions are for the purpose of satisfying the one-hour ozone attainment demonstration requirements of...

40 CFR 52.2585 - Control strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 5 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.2585... strategy: Ozone. (a) Disapproval—On November 6, 1986, the Wisconsin Department of Natural Resources submitted as a proposed revision to the State's ozone State Implementation Plan a site-specific reasonably...

40 CFR 52.1129 - Control strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.1129... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the Massachusetts Department...) and 182(c)(2)(B) of the Clean Air Act for the Springfield, Massachusetts serious ozone nonattainment...

40 CFR 52.1129 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.1129... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the Massachusetts Department...) and 182(c)(2)(B) of the Clean Air Act for the Springfield, Massachusetts serious ozone nonattainment...

40 CFR 52.350 - Control strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control strategy: Ozone. 52.350 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Colorado § 52.350 Control strategy: Ozone. (a) Revisions to the Colorado State Implementation Plan, 1-hour ozone NAAQS Redesignation Request and Maintenance...

40 CFR 52.2585 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.2585... strategy: Ozone. (a) Disapproval—On November 6, 1986, the Wisconsin Department of Natural Resources submitted as a proposed revision to the State's ozone State Implementation Plan a site-specific reasonably...

40 CFR 52.1129 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.1129... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the Massachusetts Department...) and 182(c)(2)(B) of the Clean Air Act for the Springfield, Massachusetts serious ozone nonattainment...

40 CFR 52.1534 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.1534... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the New Hampshire Department... revisions are for the purpose of satisfying the one-hour ozone attainment demonstration requirements of...

40 CFR 52.1534 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 4 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.1534... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the New Hampshire Department... revisions are for the purpose of satisfying the one-hour ozone attainment demonstration requirements of...

40 CFR 52.350 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.350 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Colorado § 52.350 Control strategy: Ozone. (a) Revisions to the Colorado State Implementation Plan, 1-hour ozone NAAQS Redesignation Request and Maintenance...

40 CFR 52.1534 - Control strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 4 2013-07-01 2013-07-01 false Control strategy: Ozone. 52.1534... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the New Hampshire Department... revisions are for the purpose of satisfying the one-hour ozone attainment demonstration requirements of...

Airborne measurements of turbulent trace gas fluxes and analysis of eddy structure in the convective boundary layer over complex terrain

NASA Astrophysics Data System (ADS)

Hasel, M.; Kottmeier, Ch.; Corsmeier, U.; Wieser, A.

2005-03-01

Using the new high-frequency measurement equipment of the research aircraft DO 128, which is described in detail, turbulent vertical fluxes of ozone and nitric oxide have been calculated from data sampled during the ESCOMPTE program in the south of France. Based on airborne turbulence measurements, radiosonde data and surface energy balance measurements, the convective boundary layer (CBL) is examined under two different aspects. The analysis covers boundary-layer convection with respect to (i) the control of CBL depth by surface heating and synoptic scale influences, and (ii) the structure of convective plumes and their vertical transport of ozone and nitric oxides. The orographic structure of the terrain causes significant differences between planetary boundary layer (PBL) heights, which are found to exceed those of terrain height variations on average. A comparison of boundary-layer flux profiles as well as mean quantities over flat and complex terrain and also under different pollution situations and weather conditions shows relationships between vertical gradients and corresponding turbulent fluxes. Generally, NO x transports are directed upward independent of the terrain, since primary emission sources are located near the ground. For ozone, negative fluxes are common in the lower CBL in accordance with the deposition of O 3 at the surface. The detailed structure of thermals, which largely carry out vertical transports in the boundary layer, are examined with a conditional sampling technique. Updrafts mostly contain warm, moist and NO x loaded air, while the ozone transport by thermals alternates with the background ozone gradient. Evidence for handover processes of trace gases to the free atmosphere can be found in the case of existing gradients across the boundary-layer top. An analysis of the size of eddies suggests the possibility of some influence of the heterogeneous terrain in mountainous area on the length scales of eddies.

Net ozone photochemical production over the eastern and central North Pacific as inferred from GTE/CITE 1 observations during fall 1983

NASA Technical Reports Server (NTRS)

Chameides, W. L.; Davis, D. D.; Rodgers, M. O.; Bradshaw, J.; Sandholm, S.; Sachse, G.; Hill, G.; Gregory, G.

1987-01-01

The role of photochemistry in the budget of tropospheric ozone is studied. Measurements of O3, NO, CO, H2O vapor, and temperature obtained during the fall of 1983 during the GTE/CITE project over the eastern and central North Pacific Ocean are analyzed. The effect of altitude on the measurements is discussed. The analysis reveals a correlation between ozone and NO levels; both increase in concentration and variability with altitude. It is observed that an additional source of secondary importance associated wih CO-rich air parcels exists. A photochemical model is utilized to calculate the net rate of ozone production by photochemical reactions. A net photochemical source of ozone in the free troposphere and a net sink in the boundary layer are detected. The relation between the ozone source in the free troposphere and NO is examined. It is estimated that photochemistry provides a net ozone source to the free troposphere overlying the eastern and central North Pacific Ocean of about 5 x 10 to the 10th molecules/sq cm sec and a net sink of ozone to the boundary layer overlying this region of about 3 x 10 to the 10th molecules/sq cm sec.

Deformation of the total ozone content field in the tropical zone

NASA Technical Reports Server (NTRS)

Vasilyev, Victor I.

1994-01-01

Presented are the ozone investigation results obtained in the tropical zone. Measurements of the total ozone content (TOC) were carried out by the ozonometer M-124. The ozonometer was automated to investigate the ozone intradiurnal variations and to increase precision of the TOC measurements. Obtained results allowed us to follow the effect of tropical cyclones (TC) on the TOC field. Several days before the TC formation the TOC increase is observed in daily mean course compared with the background one. Three types of trend can be singled out in the TOC intradiurnal course: zero, parabolic, quasi-linear. Maximum velocities of a trend are observed some days before the TC formation. Analogous harmonic constituents are mainly presented as spectrum of daily means of ozone, mean and absolute velocities of trend and dispersion as well as spectra of meteorological, hydrometeorological and actinometric values. Revealed is a number of day-to-day ozone variations concerned with large-scale circulations; moisture content in the atmosphere. Obtained are the data about short-period ozone waves (period less than a day). Thin-film silver sensors were used to measure the vertical ozone distribution (VOD). Atmospheric aerosol and VOD measurements were carried out simultaneously, they gave data of the VOD layered structure, where the VOD local minima coincided with the position of aerosol layers' maxima.

Improvement of the basic knowledge of the climatology of the vertical ozone layer by enhanced balloon sounding

NASA Technical Reports Server (NTRS)

Attmannspacher, W.; Hartmannsgrubber, R.; Lang, P.

1984-01-01

Balloon sounding of the ozone in the Earth atmosphere was performed in order to determine the natural behavior of ozone and its recognizable deviations. The importance of ozone in the Earth atmosphere and the orographic situation of observatories and ozone sounding statistics since 1966 are explained. The physical processes governing the total amount of ozone, and the behavior of stratospheric ozone are described. Measurements in the upper stratosphere show a decrease of the ozone partial pressure above 26 km altitude since 1977. The behavior of tropospheric ozone is discussed. Data since 1977 show increasing ozone values in the troposphere, up to 50% to 70%. This increase is independent of the solar radiation intensity and the reinforced transport of stratospheric ozone into the troposphere. The increase in the troposphere cannot compensate the stratospheric decrease.

Ground-based lidar for atmospheric boundary layer ozone measurements.

PubMed

Kuang, Shi; Newchurch, Michael J; Burris, John; Liu, Xiong

2013-05-20

Ground-based lidars are suitable for long-term ozone monitoring as a complement to satellite and ozonesonde measurements. However, current ground-based lidars are unable to consistently measure ozone below 500 m above ground level (AGL) due to both engineering issues and high retrieval sensitivity to various measurement errors. In this paper, we present our instrument design, retrieval techniques, and preliminary results that focus on the high-temporal profiling of ozone within the atmospheric boundary layer (ABL) achieved by the addition of an inexpensive and compact mini-receiver to the previous system. For the first time, to the best of our knowledge, the lowest, consistently achievable observation height has been extended down to 125 m AGL for a ground-based ozone lidar system. Both the analysis and preliminary measurements demonstrate that this lidar measures ozone with a precision generally better than ±10% at a temporal resolution of 10 min and a vertical resolution from 150 m at the bottom of the ABL to 550 m at the top. A measurement example from summertime shows that inhomogeneous ozone aloft was affected by both surface emissions and the evolution of ABL structures.

The Aura Mission and Its Application to Climate and Air Quality

NASA Technical Reports Server (NTRS)

Hilsenrath, Ernest; Schoeberl, Mark; Douglass, Anne

2003-01-01

NASA's Aura satellite is scheduled to launch in the second quarter of 2004 into a polar orbit. The Aura mission is designed to collect data to address three high priority environmental science questions: (1) Is the ozone layer recovering as expected? (2) What are the sources and processes that control tropospheric pollutants? And (3) what is the quantitative impact of constituents on climate change? Aura will answer these questions by globally measuring a comprehensive set of trace gases and aerosols in the troposphere and stratosphere. Aura data will also have applications for monitoring and predicting climate and air quality parameters. Aura s observations will continue the TOMS ozone trend record and provide an assessment as to whether the Montreal Protocol is achieving its objective. Aura will measure gases and aerosols in the upper troposphere and lower stratosphere that contribute to climate forcing. These data will be of sufficient coverage, vertical resolution, and accuracy to help constrain climate models. In addition, Aura observations of tropospheric ozone and its precursors will have regional as well as intercontinental coverage, which could improve emission inventories. Near real time data will tested for local air quality forecasts in collaboration with the US's Environmental Protection UV-B forecasts from Aura ozone and cloud cover data. An overview of Aura s instruments, data products, validation, and examples of data applications will be presented.

Analysis and validation of ozone variability observed by lidar during the ESCOMPTE-2001 campaign

NASA Astrophysics Data System (ADS)

Ancellet, G.; Ravetta, F.

2005-03-01

An ozone lidar was successfully operated as a ground-based instrument during the ESCOMPTE experiment in June/July 2001. Ozone profiles were measured between 0.5 and 5 km. Moreover, simultaneous measurements of the lidar scattering ratio (SR) at 316 nm diagnosed the diurnal evolution of the PBL top. Comparison of this data set with in-situ measurements by ultralight aircraft (ULM) and balloon soundings supports the existence of well-defined layers over the whole altitude range. Differences between measurements techniques are not due to instrumental inaccuracies but point towards the existence of ozone plumes with sharp horizontal gradients. This is indeed supported by aircraft horizontal cross-section available twice a day at two different levels in the planetary boundary layer (PBL) and the free troposphere. Analysis of the ozone data set has shown a good correlation between surface meteorological conditions, surface ozone measurements and lidar ozone profiles in the PBL. Observed ozone maxima or minima are linked either to sea breeze circulation bringing polluted air masses over the lidar or synoptic flows bringing air with background O 3 values into the region. The observed variability of the ozone field is very large over the whole altitude range. Although it is the result of local temporal variability and advection of spatial inhomogenities, the latter proved to be an important contribution.

NADPH:Quinone Oxidoreductase 1 Regulates Host Susceptibility to Ozone via Isoprostane Generation*

PubMed Central

Kummarapurugu, Apparao B.; Fischer, Bernard M.; Zheng, Shuo; Milne, Ginger L.; Ghio, Andrew J.; Potts-Kant, Erin N.; Foster, W. Michael; Soderblom, Erik J.; Dubois, Laura G.; Moseley, M. Arthur; Thompson, J. Will; Voynow, Judith A.

2013-01-01

NADPH:quinone oxidoreductase 1 (NQO1) is recognized as a major susceptibility gene for ozone-induced pulmonary toxicity. In the absence of NQO1 as can occur by genetic mutation, the human airway is protected from harmful effects of ozone. We recently reported that NQO1-null mice are protected from airway hyperresponsiveness and pulmonary inflammation following ozone exposure. However, NQO1 regenerates intracellular antioxidants and therefore should protect the individual from oxidative stress. To explain this paradox, we tested whether in the absence of NQO1 ozone exposure results in increased generation of A2-isoprostane, a cyclopentenone isoprostane that blunts inflammation. Using GC-MS, we found that NQO1-null mice had greater lung tissue levels of D2- and E2-isoprostanes, the precursors of J2- and A2-isoprostanes, both at base line and following ozone exposure compared with congenic wild-type mice. We confirmed in primary cultures of normal human bronchial epithelial cells that A2-isoprostane inhibited ozone-induced NF-κB activation and IL-8 regulation. Furthermore, we determined that A2-isoprostane covalently modified the active Cys179 domain in inhibitory κB kinase in the presence of ozone in vitro, thus establishing the biochemical basis for A2-isoprostane inhibition of NF-κB. Our results demonstrate that host factors may regulate pulmonary susceptibility to ozone by regulating the generation of A2-isoprostanes in the lung. These observations provide the biochemical basis for the epidemiologic observation that NQO1 regulates pulmonary susceptibility to ozone. PMID:23275341

75 FR 55711 - Federal Implementation Plans To Reduce Interstate Transport of Fine Particulate Matter and Ozone...

Federal Register 2010, 2011, 2012, 2013, 2014

2010-09-14

... Matter and Ozone; Correction AGENCY: Environmental Protection Agency (EPA). ACTION: Proposed rule..., Nitrogen oxides, Ozone, Particulate matter, Regional haze, Reporting and recordkeeping requirements, Sulfur...

Present state of knowledge of the upper atmosphere1993: An assessment report, part 2

NASA Technical Reports Server (NTRS)

Kurylo, Michael J.; Kaye, Jack A.; Hampson, Robert F.; Schmoltner, Anne-Marie

1994-01-01

This document is issued in response to the Clean Air Act Amendment of 1990, Public Law 101-549, which mandates that the National Aeronautics and Space Administration (NASA) and other key agencies submit triennial reports to Congress and the Environmental Protection Agency. NASA is charged with the responsibility to report on the state of our knowledge of the earth's upper atmosphere, particularly the stratosphere. Part 2 (this document) presents summaries of several scientific assessments of our current understanding of the chemical composition and physical structure of the stratosphere, in particular how the abundance and distribution of ozone is predicted to change in the future. These reviews include: (Section B) 'Scientific Assessment of Ozone Depletion: 1991'; (Section C) 'Methyl bromide and the Ozone Layer: A Summary of Current Understanding', published in 1992; (Section D) 'Concentrations, Lifetimes, and Trends of Chlorofluorocarbons (CFC's), Halons, and Related Molecules in the Atmosphere'; (Section E) 'The Atmospheric Effects of Stratospheric Aircraft: Interim Assessment Report of the NASA High-Speed Research Program'; (Section F) 'Chemical Kinetics and Photochemical Data for Use in Stratospheric Modeling'; and (Section G) a list of the contributors to this report.

On Recovery of the Ozone Layer in the Northern Hemisphere in the 21st Century

NASA Astrophysics Data System (ADS)

Larin, Igor

2014-05-01

Time recovery of the ozone layer in the latitudinal zones of 0°-85° N, 0°-30° N, 30°-60° N and 60°-85° N in the 21st century has been evaluated. Evaluations have been made using an interactive chemical dynamical radiative two-dimensional (2-D) model of the middle atmosphere Socrates (height 0-120 km). As initial data for calculations for the first time the greenhouse gas concentration scenarios of Intergovernmental Panel on Climate Change (IPCC) RCP 4.5 and RCP 6.0 have been used. According to the scenario RCP 4.5 a stabilization of the radiative forcing must occur before the end of the twenty-first century, and according to the scenario RCP 6.0 - in the 22nd century. It has been shown that under both scenarios, the recovery of the ozone layer in the northern hemisphere (0°-85° N) can take place in 2035, and in zones of 0°-30° N, 30°-60° N and 60°-85° N does in 2020, 2030 and 2035, respectively. It has been also shown that after recovery the ozone layer will continue to grow and by the end of the 21st century will reach the stationary level exceeding undisturbed level of 1960 at 2.7% (scenario RCP 4.5) and 3.6% (scenario RCP 6.0) in zone 0°-85° N. It seems to be not smaller ecological threat than depletion of the ozone layer at the end of the twentieth century. The results obtained are in good agreement with the known literary data (see, for example, Table 3-3 in "Scientific Assessment of Ozone Depletion: 2010"), indicating that the model Socrates and "concentration" scenarios of IPCC can successfully be used for such calculations.

Better estimates of Entrainment Mixing, Subsidence, and Photochemical Ozone Production using Aircraft and WRF data during the California Baseline Ozone Transport Study (CABOTS)

NASA Astrophysics Data System (ADS)

Trousdell, J.; Faloona, I. C.

2017-12-01

In situ flight data collected in the San Joaquin Valley of California during the summer of 2016 is used to measure boundary layer entrainment rates, ozone photochemical production, regional methane and NOx emissions. The San Joaquin Valley is plagued with air quality issues including a high frequency of ozone exceedances in the summer and an aerosol issue in the winter exacerbated by a complex mesoscale environment with a different mountain range on three sides creating an effective cul-de-sac which limits outflow and ventilation. In addition, higher elevation air brought over top of the valley can influence the valley air by entrainment at the top of the turbulent daytime atmospheric boundary layer. The flights were conducted during the California Baseline Ozone Transport Study (CABOTS). Flights are valley wide between the cities of Fresno and Visalia with a thorough probing of the atmospheric boundary layer (ABL) including vertical profiling to diagnose the ABL height and its growth rate. Entrainment velocities, which are the parameterized mixing of free tropospheric air into the boundary layer, are determined by a detailed budget equation of the inversion height. A novel scalar budgeting technique is then applied to expose residual terms of individual equations that amount to ozone photochemical production and emission rates, including; NOx and methane. The budget equations are closed out by our predicted entrainment velocities, time rate of change and horizontal advection all determined via flight data. The results of our NOx budget suggests that the California Air Resources Board emission estimates for soil NOx is grossly underestimated. A strong relationship between entrainment rates and vertical wind shear has been observed, suggesting a significant contribution to entrainment driven by vertical shear compared to the surface buoyancy flux which drives the turbulent vertical motions in the boundary layer.

Coagulation and oxidation for controlling ultrafiltration membrane fouling in drinking water treatment: Application of ozone at low dose in submerged membrane tank.

PubMed

Yu, Wenzheng; Graham, Nigel J D; Fowler, Geoffrey D

2016-05-15

Coagulation prior to ultrafiltration (UF) is widely applied for treating contaminated surface water sources for potable supply. While beneficial, coagulation alone is unable to control membrane fouling effectively in many cases, and there is continuing interest in the use of additional, complementary methods such as oxidation in the pre-treatment of raw water prior to UF. In this study, the application of ozone at low dose in the membrane tank immediately following coagulation has been evaluated at laboratory-scale employing model raw water. In parallel tests with and without the application of ozone, the impact of applied ozone doses of 0.5 mg L(-1) and 1.5 mg L(-1) (approximately 0.18 mg L(-1) and 0.54 mg L(-1) consumed ozone, respectively) on the increase of trans-membrane pressure (TMP) was evaluated and correlated with the quantity and nature of membrane deposits, both as a cake layer and within membrane pores. The results showed that a dose of 0.5 mgO3 L(-1) gave a membrane fouling rate that was substantially lower than without ozone addition, while a dose of 1.5 mgO3 L(-1) was able to prevent fouling effects significantly (no increase in TMP). Ozone was found to decrease the concentration of bacteria (especially the concentration of bacteria per suspended solid) in the membrane tank, and to alter the nature of dissolved organic matter by increasing the proportion of hydrophilic substances. Ozone decreased the concentration of extracellular polymeric substances (EPS), such as polysaccharides and proteins, in the membrane cake layer; the reduced EPS and bacterial concentrations resulted in a much thinner cake layer, although the suspended solids concentration was much higher in the ozone added membrane tank. Ozone also decreased the accumulation and hydrophobicity of organic matter within the membrane pores, leading to minimal irreversible fouling. Therefore, the application of low-dose ozone within the UF membrane tank is a potentially important approach for fully mitigating membrane fouling. Crown Copyright © 2016. Published by Elsevier Ltd. All rights reserved.

40 CFR 52.66 - Control Strategy: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control Strategy: Ozone. 52.66 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Alabama § 52.66 Control Strategy: Ozone. (a) The redesignation request submitted by the State of Alabama, on March 16, 1995 for the Birmingham marginal ozone...

40 CFR 52.1582 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 4 2014-07-01 2014-07-01 false Control strategy and regulations: Ozone... Control strategy and regulations: Ozone. (a) Subchapter 16 of the New Jersey Administrative Code, entitled... of the 1990 Clean Air Act. (d)(1) The base year ozone precursor emission inventory requirement of...

40 CFR 52.66 - Control Strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control Strategy: Ozone. 52.66 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Alabama § 52.66 Control Strategy: Ozone. (a) The redesignation request submitted by the State of Alabama, on March 16, 1995 for the Birmingham marginal ozone...

40 CFR 52.582 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.582 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Georgia § 52.582 Control strategy: Ozone. (a) Approval... area has attaining data for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR...

77 FR 6796 - Notification of a Public Meeting of the Clean Air Scientific Advisory Committee (CASAC); Ozone...

Federal Register 2010, 2011, 2012, 2013, 2014

2012-02-09

... Scientific Advisory Committee (CASAC); Ozone Review Panel AGENCY: Environmental Protection Agency (EPA... teleconference of the CASAC Ozone Review Panel to discuss its draft review of EPA's Integrated Science Assessment for Ozone and Related Photochemical Oxidants (Second External Review Draft--September 2011). DATES...

40 CFR 52.2037 - Control strategy plans for attainment and rate-of-progress: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... and rate-of-progress: Ozone. 52.2037 Section 52.2037 Protection of Environment ENVIRONMENTAL... (CONTINUED) Pennsylvania § 52.2037 Control strategy plans for attainment and rate-of-progress: Ozone. (a) Part D—Conditional Approval—the Pennsylvania plan for carbon monoxide and ozone is approved provided...

40 CFR 52.2088 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control strategy: Ozone. 52.2088... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the Rhode Island Department of...) of the Clean Air Act, for the Providence serious ozone nonattainment area. (b) Approval—Revisions to...

40 CFR 52.476 - Control strategy: ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control strategy: ozone. 52.476 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS District of Columbia § 52.476 Control strategy: ozone. (a... of Progress Plan for the District of Columbia's portion of the Metropolitan Washington, D.C. ozone...

76 FR 72919 - Draft Integrated Science Assessment for Ozone and Related Photochemical Oxidants

Federal Register 2010, 2011, 2012, 2013, 2014

2011-11-28

... Science Assessment for Ozone and Related Photochemical Oxidants AGENCY: Environmental Protection Agency... Draft Integrated Science Assessment for Ozone and Related Photochemical Oxidants'' (EPA/600/R-10/076B... national ambient air quality standards (NAAQS) for ozone. DATES: The public comment period began on...

76 FR 60820 - Draft Integrated Science Assessment for Ozone and Related Photochemical Oxidants

Federal Register 2010, 2011, 2012, 2013, 2014

2011-09-30

... Science Assessment for Ozone and Related Photochemical Oxidants AGENCY: Environmental Protection Agency... Review Draft Integrated Science Assessment for Ozone and Related Photochemical Oxidants'' (EPA/600/R-10... standards (NAAQS) for ozone. EPA is releasing this draft document to seek review by the Clean Air Scientific...

40 CFR 52.66 - Control Strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control Strategy: Ozone. 52.66 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Alabama § 52.66 Control Strategy: Ozone. (a) The redesignation request submitted by the State of Alabama, on March 16, 1995 for the Birmingham marginal ozone...

40 CFR 52.2125 - Control strategy: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 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 bi... for the 1997 8-hour ozone NAAQS. This determination, in accordance with 40 CFR 51.918, suspends the...

40 CFR 52.476 - Control strategy: ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy: ozone. 52.476 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS District of Columbia § 52.476 Control strategy: ozone. (a... of Progress Plan for the District of Columbia's portion of the Metropolitan Washington, D.C. ozone...

40 CFR 52.2088 - Control strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Control strategy: Ozone. 52.2088... strategy: Ozone. (a) Revisions to the State Implementation Plan submitted by the Rhode Island Department of...) of the Clean Air Act, for the Providence serious ozone nonattainment area. (b) Approval—Revisions to...

77 FR 24440 - Approval and Promulgation of Implementation Plans; Georgia; Atlanta; Ozone 2002 Base Year...

Federal Register 2010, 2011, 2012, 2013, 2014

2012-04-24

... Promulgation of Implementation Plans; Georgia; Atlanta; Ozone 2002 Base Year Emissions Inventory AGENCY: Environmental Protection Agency (EPA). ACTION: Proposed rule. SUMMARY: EPA is proposing to approve the ozone... (hereafter referred to as ``the Atlanta Area'' or ``Area''), ozone attainment demonstration that was...

40 CFR 52.2037 - Control strategy plans for attainment and rate-of-progress: Ozone.

Code of Federal Regulations, 2013 CFR

2013-07-01

... and rate-of-progress: Ozone. 52.2037 Section 52.2037 Protection of Environment ENVIRONMENTAL... (CONTINUED) Pennsylvania § 52.2037 Control strategy plans for attainment and rate-of-progress: Ozone. (a) Part D—Conditional Approval—the Pennsylvania plan for carbon monoxide and ozone is approved provided...

40 CFR 52.582 - Control strategy: Ozone.

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control strategy: Ozone. 52.582 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Georgia> § 52.582 Control strategy: Ozone. Link to an... of the user, the added text is set forth as follows: § 52.582 Control strategy: Ozone. (d...

76 FR 17121 - Draft Integrated Science Assessment for Ozone and Related Photochemical Oxidants

Federal Register 2010, 2011, 2012, 2013, 2014

2011-03-28

... Science Assessment for Ozone and Related Photochemical Oxidants AGENCY: Environmental Protection Agency... Draft Integrated Science Assessment for Ozone and Related Photochemical Oxidants'' (EPA/600/R-10/076A... ambient air quality standards (NAAQS) for ozone. DATES: The public comment period began on February 28...

40 CFR 52.66 - Control Strategy: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 3 2010-07-01 2010-07-01 false Control Strategy: Ozone. 52.66 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Alabama § 52.66 Control Strategy: Ozone. (a) The redesignation request submitted by the State of Alabama, on March 16, 1995 for the Birmingham marginal ozone...

40 CFR 52.1582 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 4 2012-07-01 2012-07-01 false Control strategy and regulations: Ozone... Control strategy and regulations: Ozone. (a) Subchapter 16 of the New Jersey Administrative Code, entitled... of the 1990 Clean Air Act. (d)(1) The base year ozone precursor emission inventory requirement of...

40 CFR 52.2038 - Rate of Progress Plans: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Rate of Progress Plans: Ozone. 52.2038... Progress Plans: Ozone. (a) EPA grants full approval to Pennsylvania's 15 Percent Rate of Progress Plan for the Pittsburgh-Beaver Valley ozone nonattainment area, submitted by the Secretary of the Pennsylvania...

40 CFR 52.523 - Control strategy: Ozone

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 3 2013-07-01 2013-07-01 false Control strategy: Ozone 52.523 Section...) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Florida § 52.523 Control strategy: Ozone (a) Disapproval. EPA is disapproving portions of Florida's infrastructure SIP for the 1997 8-hour ozone NAAQS regarding...

40 CFR 52.2275 - Control strategy and regulations: Ozone.

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 5 2012-07-01 2012-07-01 false Control strategy and regulations: Ozone... strategy and regulations: Ozone. (a) Section 510.3 of revised Regulation V, which was submitted by the..., 2003, concerning the Victoria County 1-hour ozone maintenance plan. This SIP revision was adopted by...

40 CFR 52.2038 - Rate of Progress Plans: Ozone.

Code of Federal Regulations, 2010 CFR

2010-07-01

... 40 Protection of Environment 4 2010-07-01 2010-07-01 false Rate of Progress Plans: Ozone. 52.2038... Progress Plans: Ozone. (a) EPA grants full approval to Pennsylvania's 15 Percent Rate of Progress Plan for the Pittsburgh-Beaver Valley ozone nonattainment area, submitted by the Secretary of the Pennsylvania...