WorldWideScience

Sample records for surface ozone depletion

  1. Airborne lidar measurements of surface ozone depletion over Arctic sea ice

    Directory of Open Access Journals (Sweden)

    J. A. Seabrook

    2013-06-01

    Full Text Available A differential absorption lidar (DIAL for measurement of atmospheric ozone concentration was operated aboard the Polar 5 research aircraft in order to study the depletion of ozone over Arctic sea ice. The lidar measurements during a flight over the sea ice north of Barrow, Alaska, on 3 April 2011 found a surface boundary layer depletion of ozone over a range of 300 km. The photochemical destruction of surface level ozone was strongest at the most northern point of the flight, and steadily decreased towards land. All the observed ozone-depleted air throughout the flight occurred within 300 m of the sea ice surface. A back-trajectory analysis of the air measured throughout the flight indicated that the ozone-depleted air originated from over the ice. Air at the surface that was not depleted in ozone had originated from over land. An investigation into the altitude history of the ozone-depleted air suggests a strong inverse correlation between measured ozone concentration and the amount of time the air directly interacted with the sea ice.

  2. Cyclone-induced surface ozone and HDO depletion in the Arctic

    Science.gov (United States)

    Zhao, Xiaoyi; Weaver, Dan; Bognar, Kristof; Manney, Gloria; Millán, Luis; Yang, Xin; Eloranta, Edwin; Schneider, Matthias; Strong, Kimberly

    2017-12-01

    Ground-based, satellite, and reanalysis datasets were used to identify two similar cyclone-induced surface ozone depletion events at Eureka, Canada (80.1° N, 86.4° W), in March 2007 and April 2011. These two events were coincident with observations of hydrogen deuterium oxide (HDO) depletion, indicating that condensation and sublimation occurred during the transport of the ozone-depleted air masses. Ice clouds (vapour and crystals) and aerosols were detected by lidar and radar when the ozone- and HDO-depleted air masses arrived over Eureka. For the 2007 event, an ice cloud layer was coincident with an aloft ozone depletion layer at 870 m altitude on 2-3 March, indicating this ice cloud layer contained bromine-enriched blowing-snow particles. Over the following 3 days, a shallow surface ozone depletion event (ODE) was observed at Eureka after the precipitation of bromine-enriched particles onto the local snowpack. A chemistry-climate model (UKCA) and a chemical transport model (pTOMCAT) were used to simulate the surface ozone depletion events. Incorporating the latest surface snow salinity data obtained for the Weddell Sea into the models resulted in improved agreement between the modelled and measured BrO concentrations above Eureka. MERRA-2 global reanalysis data and the FLEXPART particle dispersion model were used to study the link between the ozone and HDO depletion. In general, the modelled ozone and BrO showed good agreement with the ground-based observations; however, the modelled BrO and ozone in the near-surface layer are quite sensitive to the snow salinity. HDO depletion observed during these two blowing-snow ODEs was found to be weaker than pure Rayleigh fractionation. This work provides evidence of a blowing-snow sublimation process, which is a key step in producing bromine-enriched sea-salt aerosol.

  3. Addressing Ozone Layer Depletion

    Science.gov (United States)

    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.

  4. Ozone depletion update.

    Science.gov (United States)

    Coldiron, B M

    1996-03-01

    Stratospheric ozone depletion due to chlorofluorocarbons an d increased ultraviolet radiation penetration has long been predicted. To determine if predictions of ozone depletion are correct and, if so, the significance of this depletion. Review of the English literature regarding ozone depletion and solar ultraviolet radiation. The ozone layer is showing definite thinning. Recently, significantly increased ultraviolet radiation transmission has been detected at ground level at several metering stations. It appears that man-made aerosols (air pollution) block increased UVB transmission in urban areas. Recent satellite measurements of stratospheric fluorine levels more directly implicate chlorofluorocarbons as a major source of catalytic stratospheric chlorine, although natural sources may account for up to 40% of stratospheric chlorine. Stratospheric chlorine concentrations, and resultant increased ozone destruction, will be enhanced for at least the next 70 years. The potential for increased transmission of ultraviolet radiation will exist for the next several hundred years. While little damage due to increased ultraviolet radiation has occurred so far, the potential for long-term problems is great.

  5. Ozone-depleting Substances (ODS)

    Data.gov (United States)

    U.S. Environmental Protection Agency — This site includes all of the ozone-depleting substances (ODS) recognized by the Montreal Protocol. The data include ozone depletion potentials (ODP), global warming...

  6. Response of Antarctic sea surface temperature and sea ice to ozone depletion

    Science.gov (United States)

    Ferreira, D.; Gnanadesikan, A.; Kostov, Y.; Marshall, J.; Seviour, W.; Waugh, D.

    2017-12-01

    The influence of the Antarctic ozone hole extends all the way from the stratosphere through the troposphere down to the surface, with clear signatures on surface winds, and SST during summer. In this talk we discuss the impact of these changes on the ocean circulation and sea ice state. We are notably motivated by the observed cooling of the surface Southern Ocean and associated increase in Antarctic sea ice extent since the 1970s. These trends are not reproduced by CMIP5 climate models, and the underlying mechanism at work in nature and the models remain unexplained. Did the ozone hole contribute to the observed trends?Here, we review recent advances toward answering these issues using "abrupt ozone depletion" experiments. The ocean and sea ice response is rather complex, comprising two timescales: a fast ( 1-2y) cooling of the surface ocean and sea ice cover increase, followed by a slower warming trend, which, depending on models, flip the sign of the SST and sea ice responses on decadal timescale. Although the basic mechanism seems robust, comparison across climate models reveal large uncertainties in the timescales and amplitude of the response to the extent that even the sign of the ocean and sea ice response to ozone hole and recovery remains unconstrained. After briefly describing the dynamics and thermodynamics behind the two-timescale response, we will discuss the main sources of uncertainties in the modeled response, namely cloud effects and air-sea heat exchanges, surface wind stress response and ocean eddy transports. Finally, we will consider the implications of our results on the ability of coupled climate models to reproduce observed Southern Ocean changes.

  7. Ozone depletion calculations

    International Nuclear Information System (INIS)

    Luther, F.M.; Chang, J.S.; Wuebbles, D.J.; Penner, J.E.

    1992-01-01

    Models of stratospheric chemistry have been primarily directed toward an understanding of the behavior of stratospheric ozone. Initially this interest reflected the diagnostic role of ozone in the understanding of atmospheric transport processes. More recently, interest in stratospheric ozone has arisen from concern that human activities might affect the amount of stratospheric ozone, thereby affecting the ultraviolet radiation reaching the earth's surface and perhaps also affecting the climate with various potentially severe consequences for human welfare. This concern has inspired a substantial effort to develop both diagnostic and prognostic models of stratospheric ozone. During the past decade, several chemical agents have been determined to have potentially significant impacts on stratospheric ozone if they are released to the atmosphere in large quantities. These include oxides of nitrogen, oxides of hydrogen, chlorofluorocarbons, bromine compounds, fluorine compounds and carbon dioxide. In order to assess the potential impact of the perturbations caused by these chemicals, mathematical models have been developed to handle the complex coupling between chemical, radiative, and dynamical processes. Basic concepts in stratospheric modeling are reviewed

  8. Children's Models of the Ozone Layer and Ozone Depletion.

    Science.gov (United States)

    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…

  9. Ozone depletion: implications for the veterinarian.

    Science.gov (United States)

    Kopecky, K E

    1978-09-15

    Man has inadvertently modified the stratosphere. There is a good possibility that the ozone layer is being depleted by the use of jet aircraft (SST), chlorofluoromethane propellants, and nitrogen fertilizers. Under unpolluted conditions, the production of ozone equals its destruction. By man's intervention, however, the destruction may exceed the production. The potential outcome is increased intensity of solar ultraviolet (280-400 nm) radiation and penetration to the earth's surface of previously absorbed wavelengths below about 280 nm. The increased ultraviolet radiation would increase the likelihood of skin cancer in man and ocular squamous cell carcinoma in cattle. The climate also might be modified, possibly in an undesirable way.

  10. Ozone depletion and chlorine loading potentials

    Science.gov (United States)

    Pyle, John A.; Wuebbles, Donald J.; Solomon, Susan; Zvenigorodsky, Sergei; Connell, Peter; Ko, Malcolm K. W.; Fisher, Donald A.; Stordal, Frode; Weisenstein, Debra

    1991-01-01

    The recognition of the roles of chlorine and bromine compounds in ozone depletion has led to the regulation or their source gases. Some source gases are expected to be more damaging to the ozone layer than others, so that scientific guidance regarding their relative impacts is needed for regulatory purposes. Parameters used for this purpose include the steady-state and time-dependent chlorine loading potential (CLP) and the ozone depletion potential (ODP). Chlorine loading potentials depend upon the estimated value and accuracy of atmospheric lifetimes and are subject to significant (approximately 20-50 percent) uncertainties for many gases. Ozone depletion potentials depend on the same factors, as well as the evaluation of the release of reactive chlorine and bromine from each source gas and corresponding ozone destruction within the stratosphere.

  11. Global Warming: Lessons from Ozone Depletion

    Science.gov (United States)

    Hobson, Art

    2010-01-01

    My teaching and textbook have always covered many physics-related social issues, including stratospheric ozone depletion and global warming. The ozone saga is an inspiring good-news story that's instructive for solving the similar but bigger problem of global warming. Thus, as soon as students in my physics literacy course at the University of…

  12. Ozone depleting substances management inventory system

    Directory of Open Access Journals (Sweden)

    Felix Ivan Romero Rodríguez

    2018-02-01

    Full Text Available Context: The care of the ozone layer is an activity that contributes to the planet's environmental stability. For this reason, the Montreal Protocol is created to control the emission of substances that deplete the ozone layer and reduce its production from an organizational point of view. However, it is also necessary to have control of those that are already circulating and those present in the equipment that cannot be replaced yet because of the context of the companies that keep it. Generally, the control mechanisms for classifying the type of substances, equipment and companies that own them, are carried in physical files, spreadsheets and text documents, which makes it difficult to control and manage the data stored in them. Method: The objective of this research is to computerize the process of control of substances that deplete the ozone layer. An evaluation and description of all process to manage Ozone-Depleting Substances (ODS, and its alternatives, is done. For computerization, the agile development methodology SCRUM is used, and for the technological solution tools and free open source technologies are used. Result: As a result of the research, a computer tool was developed that automates the process of control and management of substances that exhaust the ozone layer and its alternatives. Conclusions: The developed computer tool allows to control and manage the ozone-depleting substances and the equipment that use them. It also manages the substances that arise as alternatives to be used for the protection of the ozone layer.

  13. The depletion of the stratospheric ozone layer

    International Nuclear Information System (INIS)

    Sabogal Nelson

    2000-01-01

    The protection of the Earth's ozone layer is of the highest importance to mankind. The dangers of its destruction are by now well known. The depletion of that layer has reached record levels. The Antarctic ozone hole covered this year a record area. The ozone layer is predicted to begin recovery in the next one or two decades and should be restored to pre-1980 levels by 2050. This is the achievement of the regime established by the 1985 Vienna Convention for the Protection of the Ozone Layer and the 1987 Montreal Protocol on Substances that Deplete the Ozone Layer. The regime established by these two agreements has been revised, and made more effective in London (1990), Copenhagen (1992), Vienna (1995), and Beijing (1999)

  14. Surface Crystallization of Cloud Droplets: Implications for Climate Change and Ozone Depletion

    Science.gov (United States)

    Tabazadeh, A.; Djikaev, Y. S.; Reiss, H.; Gore, Warren J. (Technical Monitor)

    2002-01-01

    The process of supercooled liquid water crystallization into ice is still not well understood. Current experimental data on homogeneous freezing rates of ice nucleation in supercooled water droplets show considerable scatter. For example, at -33 C, the reported freezing nucleation rates vary by as much as 5 orders of magnitude, which is well outside the range of measurement uncertainties. Until now, experimental data on the freezing of supercooled water has been analyzed under the assumption that nucleation of ice took place in the interior volume of a water droplet. Here, the same data is reanalyzed assuming that the nucleation occurred "pseudoheterogeneously" at the air (or oil)-liquid water interface of the droplet. Our analysis suggest that the scatter in the nucleation data can be explained by two main factors. First, the current assumption that nucleation occurs solely inside the volume of a water droplet is incorrect. Second, because the nucleation process most likely occurs on the surface, the rates of nuclei formation could differ vastly when oil or air interfaces are involved. Our results suggest that ice freezing in clouds may initiate on droplet surfaces and such a process can allow for low amounts of liquid water (approx. 0.002 g per cubic meters) to remain supercooled down to -40 C as observed in the atmosphere.

  15. The sensitivity of polar ozone depletion to proposed geoengineering schemes.

    Science.gov (United States)

    Tilmes, Simone; Müller, Rolf; Salawitch, Ross

    2008-05-30

    The large burden of sulfate aerosols injected into the stratosphere by the eruption of Mount Pinatubo in 1991 cooled Earth and enhanced the destruction of polar ozone in the subsequent few years. The continuous injection of sulfur into the stratosphere has been suggested as a "geoengineering" scheme to counteract global warming. We use an empirical relationship between ozone depletion and chlorine activation to estimate how this approach might influence polar ozone. An injection of sulfur large enough to compensate for surface warming caused by the doubling of atmospheric CO2 would strongly increase the extent of Arctic ozone depletion during the present century for cold winters and would cause a considerable delay, between 30 and 70 years, in the expected recovery of the Antarctic ozone hole.

  16. Producing, Importing, and Exporting Ozone-Depleting Substances

    Science.gov (United States)

    Overview page provides links to information on producing, importing, and exporting ozone-depleting substances, including information about the HCFC allowance system, importing, labeling, recordkeeping and reporting.

  17. Fundamental differences between Arctic and Antarctic ozone depletion

    OpenAIRE

    Solomon, Susan; Haskins, Jessica; Ivy, Diane J.; Min, Flora

    2014-01-01

    Fundamental differences in observed ozone depletion between the Arctic and the Antarctic are shown, clarifying distinctions between both average and extreme ozone decreases in the two hemispheres. Balloon-borne and satellite measurements in the heart of the ozone layer near 18−24 km altitude show that extreme ozone decreases often observed in the Antarctic ozone hole region have not yet been measured in the Arctic in any year, including the unusually cold Arctic spring of 2011. The data provi...

  18. Effect of greenhouse gas emissions on stratospheric ozone depletion

    NARCIS (Netherlands)

    Velders GJM; LLO

    1997-01-01

    The depletion of the ozone layer is caused mainly by the increase in emissions of chlorine- and bromine-containing compounds like CFCs, halons, carbon tetrachloride, methyl chloroform and methyl bromide. Emissions of greenhouse gases can affect the depletion of the ozone layer through atmospheric

  19. International aspects of restrictions of ozone-depleting substances

    Energy Technology Data Exchange (ETDEWEB)

    McDonald, S.C.

    1989-10-01

    This report summarizes international efforts to protect stratospheric ozone. Also included in this report is a discussion of activities in other countries to meet restrictions in the production and use of ozone-depleting substances. Finally, there is a brief presentation of trade and international competitiveness issues relating to the transition to alternatives for the regulated chlorofluorocarbons (CFCs) and halons. The stratosphere knows no international borders. Just as the impact of reduced stratospheric ozone will be felt internationally, so protection of the ozone layer is properly an international effort. Unilateral action, even by a country that produces and used large quantities of ozone-depleting substances, will not remedy the problem of ozone depletion if other countries do not follow suit. 32 refs., 7 tabs.

  20. Ozone depletion, greenhouse gases, and climate change

    Science.gov (United States)

    Mooney, Harold A.; Baker, D. James, Jr.; Bretherton, Francis P.; Burke, Kevin C.; Clark, William C.; Davis, Margaret B.; Dickinson, Robert E.; Imbrie, John; Malone, Thomas F.; Mcelroy, Michael B.

    1989-01-01

    This symposium was organized to study the unusual convergence of a number of observations, both short and long term that defy an integrated explanation. Of particular importance are surface temperature observations and observations of upper atmospheric temperatures, which have declined significantly in parts of the stratosphere. There has also been a dramatic decline in ozone concentration over Antarctica that was not predicted. Significant changes in precipitation that seem to be latitude dependent have occurred. There has been a threefold increase in methane in the last 100 years; this is a problem because a source does not appear to exist for methane of the right isotopic composition to explain the increase. These and other meteorological global climate changes are examined in detail.

  1. Ozone Layer Depletion: A Review | Eze | Nigerian Journal of Health ...

    African Journals Online (AJOL)

    There are many situations where human activities have significant effects on the environment. Ozone layer damage is one of them. The objective of this paper is to review the origin, causes, mechanisms and bioeffects of ozone layer depletion as well as the protective measures of this vanishing layer. The chlorofluorocarbon ...

  2. Newly detected ozone-depleting substances in the atmosphere

    NARCIS (Netherlands)

    Laube, Johannes C.; Newland, Mike J.; Hogan, Christopher; Brenninkmeijer, Carl A M; Fraser, Paul J.; Martinerie, Patricia; Oram, David E.; Reeves, Claire E.; Röckmann, Thomas|info:eu-repo/dai/nl/304838233; Schwander, Jakob; Witrant, Emmanuel; Sturges, William T.

    2014-01-01

    Ozone-depleting substances emitted through human activities cause large-scale damage to the stratospheric ozone layer, and influence global climate. Consequently, the production of many of these substances has been phased out; prominent examples are the chlorofluorocarbons (CFCs), and their

  3. Role of the boundary layer in the occurrence and termination of the tropospheric ozone depletion events in polar spring

    Science.gov (United States)

    Cao, Le; Platt, Ulrich; Gutheil, Eva

    2016-05-01

    Tropospheric ozone depletion events (ODEs) in the polar spring are frequently observed in a stable boundary layer condition, and the end of the events occurs when there is a breakup of the boundary layer. In order to improve the understanding of the role of the boundary layer in the ozone depletion event, a one-dimensional model is developed, focusing on the occurrence and the termination period of the ozone depletion episode. A module accounting for the vertical air transport is added to a previous box model, and a first-order parameterization is used for the estimation of the vertical distribution of the turbulent diffusivity. Simulations are performed for different strengths of temperature inversion as well as for different wind speeds. The simulation results suggest that the reactive bromine species released from the underlying surface into the lowest part of the troposphere initially stay in the boundary layer, leading to an increase of the bromine concentration. This bromine accumulation causes the ozone destruction below the top of the boundary layer. After the ozone is totally depleted, if the temperature inversion intensity decreases or the wind speed increases, the severe ozone depletion event tends to transit into a partial ozone depletion event or it recovers to the normal ozone background level of 30-40 ppb. This recovery process takes about 2 h. Due to the presence of high-level HBr left from the initial occurrence of ODEs, the complete removal of ozone in the boundary layer is achieved a few days after the first termination of ODE. The time required for the recurrence of the ozone depletion in a 1000 m boundary layer is approximately 5 days, while the initial occurrence of the complete ozone consumption takes 15 days. The present model is suitable to clarify the reason for both the start and the termination of the severe ozone depletion as well as the partial ozone depletion in the observations.

  4. From ozone depletion to biological UV damage

    Energy Technology Data Exchange (ETDEWEB)

    Tamm, E.; Thomalla, E.; Koepke, P. [Munich Univ. (Germany). Meteorological Inst.

    1995-12-31

    Based on the ozone data from the Meteorological Observatory Hohenpeissenberg (MOHP: 47.8 deg N, 11.01 deg E) and corresponding mean atmospheric conditions, high resolution UV spectra are calculated with a complex radiation transfer model STAR. Biologically weighted UV spectra are investigated as integrated irradiances (dose rates) for maximum zenith angles and as daily integrals for selected days of the year. Ozone variation and uncertainty of action spectra are investigated

  5. OZONE DEPLETING SUBSTANCES ELIMINATION MANAGEMENT: THE SUCCESS STORY OF MACEDONIA

    Directory of Open Access Journals (Sweden)

    Margarita Matlievska

    2013-04-01

    Full Text Available Man, with its activities, produces and uses substances that have negative impact on the environment and the human health, and can cause an economic damage. Consequently, they have a great impact on quality of life. Among the most harmful chemicals are Ozone Depleting Substances that are subject of regulation with international conventions. This Paper supports the fact that each country has to undertake national efforts for ozone depleting substances reduction and elimination. In that respect, the general objective of the Paper is to present the Macedonian unique experience regarding its efforts to reduce or eliminate these substances. The following two aspects were subject to the research: national legislation which regulates the Ozone Depleting Substances import and export as well as the implementation of the projects that resulted with the elimination of Ozone Depleting Substances quantities in the period 1995 – 2010. The research outcomes confirm the starting research hypothesis i.e. that with adequately created and implemented national action, the amount of Ozone Depleting Substances consumption can dramatically fall.

  6. Ozone layer depletion simulation in an Environmental Chemistry course.

    Science.gov (United States)

    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.

  7. Observations of ozone depletion events in a Finnish boreal forest

    Directory of Open Access Journals (Sweden)

    X. Chen

    2018-01-01

    Full Text Available We investigated the concentrations and vertical profiles of ozone over a 20-year period (1996–2016 at the SMEAR II station in southern Finland. Our results showed that the typical daily median ozone concentrations were in the range of 20–50 ppb with clear diurnal and annual patterns. In general, the profile of ozone concentrations illustrated an increase as a function of heights. The main aim of our study was to address the frequency and strength of ozone depletion events at this boreal forest site. We observed more than a thousand of 10 min periods at 4.2 m, with ozone concentrations below 10 ppb, and a few tens of cases with ozone concentrations below 2 ppb. Among these observations, a number of ozone depletion events that lasted for more than 3 h were identified, and they occurred mainly in autumn and winter months. The low ozone concentrations were likely related to the formation of a low mixing layer under the conditions of low temperatures, low wind speeds, high relative humidities and limited intensity of solar radiation.

  8. Observations of ozone depletion events in a Finnish boreal forest

    Science.gov (United States)

    Chen, Xuemeng; Quéléver, Lauriane L. J.; Fung, Pak L.; Kesti, Jutta; Rissanen, Matti P.; Bäck, Jaana; Keronen, Petri; Junninen, Heikki; Petäjä, Tuukka; Kerminen, Veli-Matti; Kulmala, Markku

    2018-01-01

    We investigated the concentrations and vertical profiles of ozone over a 20-year period (1996-2016) at the SMEAR II station in southern Finland. Our results showed that the typical daily median ozone concentrations were in the range of 20-50 ppb with clear diurnal and annual patterns. In general, the profile of ozone concentrations illustrated an increase as a function of heights. The main aim of our study was to address the frequency and strength of ozone depletion events at this boreal forest site. We observed more than a thousand of 10 min periods at 4.2 m, with ozone concentrations below 10 ppb, and a few tens of cases with ozone concentrations below 2 ppb. Among these observations, a number of ozone depletion events that lasted for more than 3 h were identified, and they occurred mainly in autumn and winter months. The low ozone concentrations were likely related to the formation of a low mixing layer under the conditions of low temperatures, low wind speeds, high relative humidities and limited intensity of solar radiation.

  9. Implications of stratospheric ozone depletion upon plant production

    International Nuclear Information System (INIS)

    Teramura, A.H.

    1990-01-01

    An increase in the amount of UV-B radiation reaching the earth's surface is identified as the major factor of concern to result from stratospheric ozone depletion. UV radiation is believed to have wide ranging effects on plant physiology and biochemistry. In screening studies of > 300 species and cultivars, > 50% have shown sensitivity to UV radiation. The most sensitive plant families appear to be Leguminosae, Cucurbitaceae and Cruciferae. The need for a better understanding of the effects of UV radiation on crop plant physiology and particularly of the repair and protective mechanisms developed by some species is stressed. This paper was presented at a colloquium on Implications of global climate changes on horticultural cropping practices and production in developing countries held at the 86th Annual Meeting of the American Society for Horticultural Science at Tulsa, Oklahoma, on 2 Aug. 1989

  10. Ozone depletion and climate change: impacts on UV radiation.

    Science.gov (United States)

    Bais, A F; McKenzie, R L; Bernhard, G; Aucamp, P J; Ilyas, M; Madronich, S; Tourpali, K

    2015-01-01

    We assess the importance of factors that determine the intensity of UV radiation at the Earth's surface. Among these, atmospheric ozone, which absorbs UV radiation, is of considerable importance, but other constituents of the atmosphere, as well as certain consequences of climate change, can also be major influences. Further, we assess the variations of UV radiation observed in the past and present, and provide projections for the future. Of particular interest are methods to measure or estimate UV radiation at the Earth's surface. These are needed for scientific understanding and, when they are sufficiently sensitive, they can serve as monitors of the effectiveness of the Montreal Protocol and its amendments. Also assessed are several aspects of UV radiation related to biological effects and health. The implications for ozone and UV radiation from two types of geoengineering methods that have been proposed to combat climate change are also discussed. In addition to ozone effects, the UV changes in the last two decades, derived from measurements, have been influenced by changes in aerosols, clouds, surface reflectivity, and, possibly, by solar activity. The positive trends of UV radiation observed after the mid-1990s over northern mid-latitudes are mainly due to decreases in clouds and aerosols. Despite some indications from measurements at a few stations, no statistically significant decreases in UV-B radiation attributable to the beginning of the ozone recovery have yet been detected. Projections for erythemal irradiance (UVery) suggest the following changes by the end of the 21(st) century (2090-2100) relative to the present time (2010-2020): (1) Ozone recovery (due to decreasing ozone-depleting substances and increasing greenhouse gases) would cause decreases in UVery, which will be highest (up to 40%) over Antarctica. Decreases would be small (less than 10%) outside the southern Polar Regions. A possible decline of solar activity during the 21(st) century

  11. Ozone depletion, related UVB changes and increased skin cancer incidence

    Science.gov (United States)

    Kane, R. P.

    1998-03-01

    Stratospheric ozone at middle latitudes shows a seasonal variation of about +/-20%, a quasi-biennial oscillation of 1-10% range and a long-term variation in which the level was almost steady up to about 1979 and declined thereafter to the present day by about 10%. These variations are expected to be reflected in solar UVB observed at the ground, but in an opposite direction. Thus UVB should have had a long-term increase of about 10-20%, which should cause an increase in skin cancer incidence of about 20-40%. Skin cancer incidence has increased all over the world, e.g. about 90% in USA during 1974-1990. It is popularly believed that this increase in skin cancer incidence is related to the recent ozone depletion. This seems to be incorrect, for two reasons. Firstly, the observed skin cancer increase is too large (90%) compared with the expected value (40%) from ozone depletion. Secondly, cancer does not develop immediately after exposure to solar UVB. The sunburns may occur within hours; but cancer development and detection may take years, even decades. Hence the observed skin cancer increase since 1974 (no data available for earlier periods) must have occurred due to exposure to solar UVB in the 1950s and 1960s, when there was no ozone depletion. Thus, the skin cancer increase must be attributed to harmful solar UVB levels existing even in the 1960s, accentuated later not by ozone depletion (which started only much later, by 1979) but by other causes, such as a longer human life span, better screening, increasing tendencies of sunbathing at beaches, etc., in affluent societies. On the other hand, the recent ozone depletion and the associated UVB increases will certainly take their toll; only that the effects will not be noticed now but years or decades from now. The concern for the future expressed in the Montreal Protocol for reducing ozone depletion by controlling CFC production is certainly justified, especially because increased UVB is harmful to animal and

  12. Contribution of some ozone depleting substances (ODS)

    Indian Academy of Sciences (India)

    113, CH2Cl, CH3Br, CCl4, CH3CCl3, HCFCs, halons, WMO (World Meteorological Organization) minor constituents, CH4, N2O and water vapour to the variation of total column ozone (TCO) concentration at the station in Srinagar (34°N, 74.8°E) ...

  13. Contribution of some ozone depleting substances (ODS) and ...

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Earth System Science; Volume 122; Issue 1. Contribution of some ozone depleting substances (ODS) and greenhouse gases (GHGs) on total column zone growth at Srinagar (34°N, 74.8°), India. P K Jana D K Saha D Sarkar. Volume 122 Issue 1 February 2013 pp 239-252 ...

  14. Depletion of ozone layer and health

    International Nuclear Information System (INIS)

    Kripke, M.L.

    1990-01-01

    A decrease in food supply, rather than an increase in cancers, could turn out to be the greatest danger from the loss of the Earth's ozone shield says the author. This could result from alterations in plants and animals that are more sensitive than humans to increased levels of ultraviolet radiation. Increasing ambient ultraviolet radiation within a short time would exert dramatic selective pressure on all living organisms, but the global consequences of such an occurrence cannot be predicted. Common skin cancer is the best understood link with ultraviolet radiation. In fact, the link is so straightforward that precise calculations are possible: a 1% decrease in ozone equals a 2% increase in ultraviolet radiation, which translates into a 3 to 6% increase in common skin cancers in the US. If the immune system is damaged, the body cannot survive the continual onslaught of infectious agents present in the environment. People's willingness to protect themselves against sunlight exposure has been dictated by fashion. The fashionability of hats and sunglasses is beneficial for reducing the risk of cataracts; on the other hand, the fashionability of sun-tans has probably contributed to the rising incidence of skin cancer among Caucasians. The best remedy she advises is to avoid overexposure to sunlight

  15. Bromine measurements in ozone depleted air over the Arctic Ocean

    Directory of Open Access Journals (Sweden)

    J. A. Neuman

    2010-07-01

    Full Text Available In situ measurements of ozone, photochemically active bromine compounds, and other trace gases over the Arctic Ocean in April 2008 are used to examine the chemistry and geographical extent of ozone depletion in the arctic marine boundary layer (MBL. Data were obtained from the NOAA WP-3D aircraft during the Aerosol, Radiation, and Cloud Processes affecting Arctic Climate (ARCPAC study and the NASA DC-8 aircraft during the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS study. Fast (1 s and sensitive (detection limits at the low pptv level measurements of BrCl and BrO were obtained from three different chemical ionization mass spectrometer (CIMS instruments, and soluble bromide was measured with a mist chamber. The CIMS instruments also detected Br2. Subsequent laboratory studies showed that HOBr rapidly converts to Br2 on the Teflon instrument inlets. This detected Br2 is identified as active bromine and represents a lower limit of the sum HOBr + Br2. The measured active bromine is shown to likely be HOBr during daytime flights in the arctic. In the MBL over the Arctic Ocean, soluble bromide and active bromine were consistently elevated and ozone was depleted. Ozone depletion and active bromine enhancement were confined to the MBL that was capped by a temperature inversion at 200–500 m altitude. In ozone-depleted air, BrO rarely exceeded 10 pptv and was always substantially lower than soluble bromide that was as high as 40 pptv. BrCl was rarely enhanced above the 2 pptv detection limit, either in the MBL, over Alaska, or in the arctic free troposphere.

  16. Stratospheric ozone depletion from future nitrous oxide increases

    Directory of Open Access Journals (Sweden)

    W. Wang

    2014-12-01

    Full Text Available We have investigated the impact of the assumed nitrous oxide (N2O increases on stratospheric chemistry and dynamics using a series of idealized simulations with a coupled chemistry-climate model (CCM. In a future cooler stratosphere the net yield of NOy from N2O is shown to decrease in a reference run following the IPCC A1B scenario, but NOy can still be significantly increased by extra increases of N2O over 2001–2050. Over the last decade of simulations, 50% increases in N2O result in a maximal 6% reduction in ozone mixing ratios in the middle stratosphere at around 10 hPa and an average 2% decrease in the total ozone column (TCO compared with the control run. This enhanced destruction could cause an ozone decline in the first half of this century in the middle stratosphere around 10 hPa, while global TCO still shows an increase at the same time. The results from a multiple linear regression analysis and sensitivity simulations with different forcings show that the chemical effect of N2O increases dominates the N2O-induced ozone depletion in the stratosphere, while the dynamical and radiative effects of N2O increases are overall insignificant. The analysis of the results reveals that the ozone depleting potential of N2O varies with the time period and is influenced by the environmental conditions. For example, carbon dioxide (CO2 increases can strongly offset the ozone depletion effect of N2O.

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

    Science.gov (United States)

    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.

  18. The Effect of Climate Change on Ozone Depletion through Changes in Stratospheric Water Vapour

    Science.gov (United States)

    Kirk-Davidoff, Daniel B.; Hintsa, Eric J.; Anderson, James G.; Keith, David W.

    1999-01-01

    Several studies have predicted substantial increases in Arctic ozone depletion due to the stratospheric cooling induced by increasing atmospheric CO2 concentrations. But climate change may additionally influence Arctic ozone depletion through changes in the water vapor cycle. Here we investigate this possibility by combining predictions of tropical tropopause temperatures from a general circulation model with results from a one-dimensional radiative convective model, recent progress in understanding the stratospheric water vapor budget, modelling of heterogeneous reaction rates and the results of a general circulation model on the radiative effect of increased water vapor. Whereas most of the stratosphere will cool as greenhouse-gas concentrations increase, the tropical tropopause may become warmer, resulting in an increase of the mean saturation mixing ratio of water vapor and hence an increased transport of water vapor from the troposphere to the stratosphere. Stratospheric water vapor concentration in the polar regions determines both the critical temperature below which heterogeneous reactions on cold aerosols become important (the mechanism driving enhanced ozone depletion) and the temperature of the Arctic vortex itself. Our results indicate that ozone loss in the later winter and spring Arctic vortex depends critically on water vapor variations which are forced by sea surface temperature changes in the tropics. This potentially important effect has not been taken into account in previous scenarios of Arctic ozone loss under climate change conditions.

  19. Ozone sensitivity to varying greenhouse gases and ozone-depleting substances in CCMI-1 simulations

    Directory of Open Access Journals (Sweden)

    O. Morgenstern

    2018-01-01

    Full Text Available Ozone fields simulated for the first phase of the Chemistry-Climate Model Initiative (CCMI-1 will be used as forcing data in the 6th Coupled Model Intercomparison Project. Here we assess, using reference and sensitivity simulations produced for CCMI-1, the suitability of CCMI-1 model results for this process, investigating the degree of consistency amongst models regarding their responses to variations in individual forcings. We consider the influences of methane, nitrous oxide, a combination of chlorinated or brominated ozone-depleting substances, and a combination of carbon dioxide and other greenhouse gases. We find varying degrees of consistency in the models' responses in ozone to these individual forcings, including some considerable disagreement. In particular, the response of total-column ozone to these forcings is less consistent across the multi-model ensemble than profile comparisons. We analyse how stratospheric age of air, a commonly used diagnostic of stratospheric transport, responds to the forcings. For this diagnostic we find some salient differences in model behaviour, which may explain some of the findings for ozone. The findings imply that the ozone fields derived from CCMI-1 are subject to considerable uncertainties regarding the impacts of these anthropogenic forcings. We offer some thoughts on how to best approach the problem of generating a consensus ozone database from a multi-model ensemble such as CCMI-1.

  20. Estimation of surface UV levels based on Meteor-3/TOMS ozone data

    Energy Technology Data Exchange (ETDEWEB)

    Borisov, Y.A. [Central Aerological Observatory, Moscow (Russian Federation); Geogdzhaev, I.V. [Moscow Inst. of Physics and Technology, Moscow (Russian Federation); Khattatov, V.U. [Central Aerological Observatory, Moscow (Russian Federation)

    1995-12-31

    The major consequence of ozone layer depletion for the environment is an increase of harmful ultraviolet (UV) radiation on the Earth surface and in the upper ocean. This implies the importance of environmental UV monitoring. Since the direct global monitoring is not currently possible, indirect estimations of surface UV levels may be used based on satellite ozone data (Madronich, S. 1992). Total Ozone Mapping Spectrometer (TOMS) on board the METEOR-3 satellite provided regular set of data for such estimates. During the time of its operation (August, 1991 - December, 1994) the instrument registered several ozone hole events over Antarctica, when ozone levels dropped by as much as 60 % from their unperturbed values. Probably even more alarming ozone depletions were observed over highly populated regions of middle latitudes of northern hemisphere. Radiative transfer modeling was used to convert METEOR-3/TOMS daily ozone values into regional and global maps of biologically active UV. Calculations demonstrate the effect on surface UV levels produced by ozone hole over Antarctica and ozone depletions over the territory of Russia (March, 1994). UV contour lines deviate from the normal appearance which is determined by growing southward solar elevation. UV contour lines are almost perpendicular to the ozone ones in the ozone depletions areas. The 30 % ozone depletion, over Siberia caused more than 30 % increase in noontime erythemal UV levels, which is equivalent to 10-15 degrees southward latitude displacement. Higher UV radiation increases were found in ozone hole over South America (October 1992) equivalent to about 20 degrees southward displacement

  1. Quantifying the contributions to stratospheric ozone changes from ozone depleting substances and greenhouse gases

    Directory of Open Access Journals (Sweden)

    D. A. Plummer

    2010-09-01

    Full Text Available A state-of-the-art chemistry climate model coupled to a three-dimensional ocean model is used to produce three experiments, all seamlessly covering the period 1950–2100, forced by different combinations of long-lived Greenhouse Gases (GHGs and Ozone Depleting Substances (ODSs. The experiments are designed to quantify the separate effects of GHGs and ODSs on the evolution of ozone, as well as the extent to which these effects are independent of each other, by alternately holding one set of these two forcings constant in combination with a third experiment where both ODSs and GHGs vary. We estimate that up to the year 2000 the net decrease in the column amount of ozone above 20 hPa is approximately 75% of the decrease that can be attributed to ODSs due to the offsetting effects of cooling by increased CO2. Over the 21st century, as ODSs decrease, continued cooling from CO2 is projected to account for more than 50% of the projected increase in ozone above 20 hPa. Changes in ozone below 20 hPa show a redistribution of ozone from tropical to extra-tropical latitudes with an increase in the Brewer-Dobson circulation. In addition to a latitudinal redistribution of ozone, we find that the globally averaged column amount of ozone below 20 hPa decreases over the 21st century, which significantly mitigates the effect of upper stratospheric cooling on total column ozone. Analysis by linear regression shows that the recovery of ozone from the effects of ODSs generally follows the decline in reactive chlorine and bromine levels, with the exception of the lower polar stratosphere where recovery of ozone in the second half of the 21st century is slower than would be indicated by the decline in reactive chlorine and bromine concentrations. These results also reveal the degree to which GHG-related effects mute the chemical effects of N2O on ozone in the standard future scenario used for the WMO Ozone Assessment. Increases in the

  2. Ozone-depleting-substance control and phase-out plan

    International Nuclear Information System (INIS)

    Nickels, J.M.; Brown, M.J.

    1994-07-01

    Title VI of the Federal Clean Air Act Amendments of 1990 requires regulation of the use and disposal of ozone-depleting substances (ODSs) (e.g., Halon, Freon). Several important federal regulations have been promulgated that affect the use of such substances at the Hanford Site. On April 23, 1993, Executive Order (EO) 12843, Procurement Requirements and Policies for Federal Agencies for Ozone-Depleting Substances (EPA 1993) was issued for Federal facilities to conform to the new US Environmental Protection Agency (EPA) regulations implementing the Clean Air Act of 1963 (CAA), Section 613, as amended. To implement the requirements of Title VI the US Department of Energy, Richland Operations Office (RL), issued a directive to the Hanford Site contractors on May 25, 1994 (Wisness 1994). The directive assigns Westinghouse Hanford Company (WHC) the lead in coordinating the development of a sitewide comprehensive implementation plan to be drafted by July 29, 1994 and completed by September 30, 1994. The implementation plan will address several areas where immediate compliance action is required. It will identify all current uses of ODSs and inventories, document the remaining useful life of equipment that contains ODS chemicals, provide a phase-out schedule, and provide a strategy that will be implemented consistently by all the Hanford Site contractors. This plan also addresses the critical and required elements of Federal regulations, the EO, and US Department of Energy (DOE) guidance. This plan is intended to establish a sitewide management system to address the clean air requirements

  3. International regime formation: Ozone depletion and global climate change

    International Nuclear Information System (INIS)

    Busmann, N.E.

    1994-03-01

    Two theoretical perspectives, neorealism and neoliberal institutionalism, dominate in international relations. An assessment is made of whether these perspectives provide compelling explanations of why a regime with specific targets and timetables was formed for ozone depletion, while a regime with such specificity was not formed for global climate change. In so doing, the assumptions underlying neorealism and neoliberal institutionalism are examined. A preliminary assessment is offered of the policymaking and institutional bargaining process. Patterns of interstate behavior are evolving toward broader forms of cooperation, at least with regard to global environmental issues, although this process is both slow and cautious. State coalitions on specific issues are not yet powerful enough to create a strong community of states in which states are willing to devolve power to international institutions. It is shown that regime analysis is a useful analytic framework, but it should not be mistaken for theory. Regime analysis provides an organizational framework offering a set of questions regarding the principles and norms that govern cooperation and conflict in an issue area, and whether forces independent of states exist which affect the scope of state behavior. An examination of both neorealism and neoliberal institutionalism, embodied by four approaches to regime formation, demonstrates that neither has sufficient scope to account for contextual dynamics in either the ozone depletion or global climate change regime formation processes. 261 refs

  4. Newly detected ozone-depleting substances in the atmosphere

    Science.gov (United States)

    Laube, Johannes C.; Newland, Mike J.; Hogan, Christopher; Brenninkmeijer, Carl A. M.; Fraser, Paul J.; Martinerie, Patricia; Oram, David E.; Reeves, Claire E.; Röckmann, Thomas; Schwander, Jakob; Witrant, Emmanuel; Sturges, William T.

    2014-04-01

    Ozone-depleting substances emitted through human activities cause large-scale damage to the stratospheric ozone layer, and influence global climate. Consequently, the production of many of these substances has been phased out; prominent examples are the chlorofluorocarbons (CFCs), and their intermediate replacements, the hydrochlorofluorocarbons (HCFCs). So far, seven types of CFC and six types of HCFC have been shown to contribute to stratospheric ozone destruction. Here, we report the detection and quantification of a further three CFCs and one HCFC. We analysed the composition of unpolluted air samples collected in Tasmania between 1978 and 2012, and extracted from deep firn snow in Greenland in 2008, using gas chromatography with mass spectrometric detection. Using the firn data, we show that all four compounds started to emerge in the atmosphere in the 1960s. Two of the compounds continue to accumulate in the atmosphere. We estimate that, before 2012, emissions of all four compounds combined amounted to more than 74,000 tonnes. This is small compared with peak emissions of other CFCs in the 1980s of more than one million tonnes each year. However, the reported emissions are clearly contrary to the intentions behind the Montreal Protocol, and raise questions about the sources of these gases.

  5. Ozone-layer depletion and the fate of CFs

    International Nuclear Information System (INIS)

    Ghauri, B.

    1998-01-01

    The ozone layer of the stratosphere, centred at an altitude of about 25 km from the earth's surface, plays the role of absorbing ultraviolet rays contained in solar light. The known harmful effects per unit dose of the shorter wavelengths, UV-C and UV-B, are greater than those of the longer wavelength, UV-A. The UV-B radiation is the most carcinogenic part of the solar UV spectrum reaching the earth's surface. Ozone layer is being destroyed rapidly by refrigerant gases released on the Earth. As a result, the global environment and our livelihood are being seriously threatened., The destruction of the ozone layer allows more damaging ultraviolet rays to reach the earth. Ultraviolet rays cause an increase in such illnesses as skin cancer and cataract, and may even seriously affect the ecosystem. Therefore, processing refrigerant gases without discharging these into the atmosphere is now a global issue. To solve the issue, CFCs must be reprocessed for reuse by recovery and reclamation, or else we should destruct it to fluoro carbons, with recovery reclamation of fluoro carbons. This paper gives an account of the international initiatives for protection of the ozone layer and present status of the various measures taken, including substitutes for the damaging fluoro-carbons, recovery reclamation of fluoro-carbons. (author)

  6. The Effects of Volcano-Induced Ozone Depletion on Short-lived Climate Forcing in the Arctic

    Science.gov (United States)

    Ward, P. L.

    2012-12-01

    Photodissociation of oxygen maintains the stratopause ~50°C warmer than the tropopause. Photodissociation of ozone warms the lower stratosphere, preventing most of this high-energy DNA-damaging solar radiation from reaching the troposphere. Ozone depletion allows more UV energy to reach the lower troposphere causing photodissociation of anthropogenic ozone and nitrogen dioxide. UV energy also penetrates the ocean >10 m where it is absorbed more efficiently than infrared radiation that barely penetrates the surface. Manmade chlorofluorocarbons caused ozone depletion from 1965 to 1994 with slow recovery predicted over the next 50+ years. But the lowest levels of ozone followed the eruptions of Pinatubo (1991 VEI=6), Eyjafjallajökull (2010 VEI=4), and Grímsvötn (2011 VEI=4). Each of the relatively small, basaltic eruptions in Iceland caused more ozone depletion than the long-term effects of chlorofluorocarbons, although total ozone appears to return to pre-eruption levels within a decade. Ozone depletion by 20% increases energy flux thru the lowermost troposphere by 0.7 W m-2 for overhead sun causing temperatures in the lower stratosphere to drop >2°C since 1958 in steps after the 3 largest volcanic eruptions: Agung 1963, El Chichón 1982, and Pinatubo. Temperatures at the surface increased primarily in the regions and at the times of the greatest observed ozone depletion. The greatest warming observed was along the Western Antarctic Peninsula (65.4°S) where minimum temperatures rose 6.7°C from 1951 to 2003 while maximum temperatures remained relatively constant. Minimum total column ozone in September-October was 40-56% lower than in 1972 almost every year since 1987, strongly anti-correlated with observed minimum temperatures. Sea ice decreased 10%, 7 ice shelves separated, 87% of the glaciers retreated and the Antarctic Circumpolar Current warmed. Elsewhere under the ozone hole, warming of continental Antarctica was limited by the high albedo (0.86) of

  7. Numerical analysis of the chemical kinetic mechanisms of ozone depletion and halogen release in the polar troposphere

    Science.gov (United States)

    Cao, L.; Sihler, H.; Platt, U.; Gutheil, E.

    2014-04-01

    The role of halogen species (e.g., Br, Cl) in the troposphere of polar regions has been investigated since the discovery of their importance for boundary layer ozone destruction in the polar spring about 25 years ago. Halogen species take part in an auto-catalytic chemical reaction cycle, which releases Br2 and BrCl from the sea salt aerosols, fresh sea ice or snowpack, leading to ozone depletion. In this study, three different chemical reaction schemes are investigated: a bromine-only reaction scheme, which then is subsequently extended to include nitrogen-containing compounds and chlorine species and corresponding chemical reactions. The importance of specific reactions and their rate constants is identified by a sensitivity analysis. The heterogeneous reaction rates are parameterized by considering the aerodynamic resistance, a reactive surface ratio, β, i.e., the ratio of reactive surface area to total ground surface area, and the boundary layer height, Lmix. It is found that for β = 1, a substantial ozone decrease occurs after five days and ozone depletion lasts for 40 h for Lmix = 200 m. For about β ≥ 20, the time required for major ozone depletion ([O3] layer, and for β = 100 it approaches two days, 28 h of which are attributable to the induction and 20 h to the depletion time. In polar regions, a small amount of NOx may exist, which stems from nitrate contained in the snow, and may have a strong impact on the ozone depletion. Therefore, the role of nitrogen-containing species on the ozone depletion rate is studied. The results show that the NOx concentrations are influenced by different chemical reactions over different time periods. During ozone depletion, the reaction cycle involving the BrONO2 hydrolysis is dominant. A critical value of 0.0004 of the uptake coefficient of the BrONO2 hydrolysis reaction at the aerosol and saline surfaces is identified, beyond which the existence of NOx species accelerates the ozone depletion event, whereas for lower

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

    Science.gov (United States)

    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…

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

    Science.gov (United States)

    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.

  10. Can ozone depletion and global warming interact to produce rapid climate change?

    Science.gov (United States)

    Hartmann, Dennis L.; Wallace, John M.; Limpasuvan, Varavut; Thompson, David W. J.; Holton, James R.

    2000-01-01

    The atmosphere displays modes of variability whose structures exhibit a strong longitudinally symmetric (annular) component that extends from the surface to the stratosphere in middle and high latitudes of both hemispheres. In the past 30 years, these modes have exhibited trends that seem larger than their natural background variability, and may be related to human influences on stratospheric ozone and/or atmospheric greenhouse gas concentrations. The pattern of climate trends during the past few decades is marked by rapid cooling and ozone depletion in the polar lower stratosphere of both hemispheres, coupled with an increasing strength of the wintertime westerly polar vortex and a poleward shift of the westerly wind belt at the earth's surface. Annular modes of variability are fundamentally a result of internal dynamical feedbacks within the climate system, and as such can show a large response to rather modest external forcing. The dynamics and thermodynamics of these modes are such that strong synergistic interactions between stratospheric ozone depletion and greenhouse warming are possible. These interactions may be responsible for the pronounced changes in tropospheric and stratospheric climate observed during the past few decades. If these trends continue, they could have important implications for the climate of the 21st century. PMID:10677475

  11. Ozone depletion, developing countries, and human rights: Seeking better ground on which to fight for protection of the ozone layer

    Energy Technology Data Exchange (ETDEWEB)

    Williams, V.

    1995-12-31

    I urge you not to take a complacent view of the situation. The state of depletion of the ozone layer continues to be alarming... In February, 1993, the ozone levels over North America and most of Europe were 20 percent below normal... Even now, millions of tons of CFC [chlorofluorocarbon] products are en route to their fatal stratospheric rendezvous... This exponential increase calls for increased reflection on the state of the ozone layer and calls for bold decisions.

  12. Bromine atom production and chain propagation during springtime Arctic ozone depletion events in Barrow, Alaska

    Science.gov (United States)

    Thompson, Chelsea R.; Shepson, Paul B.; Liao, Jin; Huey, L. Greg; Cantrell, Chris; Flocke, Frank; Orlando, John

    2017-03-01

    Ozone depletion events (ODEs) in the Arctic are primarily controlled by a bromine radical-catalyzed destruction mechanism that depends on the efficient production and recycling of Br atoms. Numerous laboratory and modeling studies have suggested the importance of heterogeneous recycling of Br through HOBr reaction with bromide on saline surfaces. On the other hand, the gas-phase regeneration of bromine atoms through BrO-BrO radical reactions has been assumed to be an efficient, if not dominant, pathway for Br reformation and thus ozone destruction. Indeed, it has been estimated that the rate of ozone depletion is approximately equal to twice the rate of the BrO self-reaction. Here, we use a zero-dimensional, photochemical model, largely constrained to observations of stable atmospheric species from the 2009 Ocean-Atmosphere-Sea Ice-Snowpack (OASIS) campaign in Barrow, Alaska, to investigate gas-phase bromine radical propagation and recycling mechanisms of bromine atoms for a 7-day period during late March. This work is a continuation of that presented in Thompson et al. (2015) and utilizes the same model construct. Here, we use the gas-phase radical chain length as a metric for objectively quantifying the efficiency of gas-phase recycling of bromine atoms. The gas-phase bromine chain length is determined to be quite small, at < 1.5, and highly dependent on ambient O3 concentrations. Furthermore, we find that Br atom production from photolysis of Br2 and BrCl, which is predominately emitted from snow and/or aerosol surfaces, can account for between 30 and 90 % of total Br atom production. This analysis suggests that condensed-phase production of bromine is at least as important as, and at times greater than, gas-phase recycling for the occurrence of Arctic ODEs. Therefore, the rate of the BrO self-reaction is not a sufficient estimate for the rate of O3 depletion.

  13. Consequences of ozone depletion for terrestrial plant productivity

    International Nuclear Information System (INIS)

    Teramura, A.H.

    1994-01-01

    Many plants are greatly affected by increases in UV-B radiation but there is tremendous variability in their sensitivity. Plants have evolved natural adaptations such as anatomical, morphological and biochemical features which protect them from UV-B radiation. The extent of these natural adaptations may be related to the geographic origin of the species. For example, species originating from areas receiving high ambient levels of UV-B radiation were found to be highly resistant to UV-B radiation. In sensitive species, photosynthetic activity may be reduced by direct effects on photosynthetic enzymes and metabolic pathways or by indirect effects on photosynthetic pigments or stomatal function. The fluence response of these changes has yet to be clearly demonstrated in most cases. These biochemical and physiological responses may result in reduced growth (plant height, dry weight, leaf area, etc.) photosynthetic activity and flowering. Approximately half of the species tested appear sensitive and sensitivity also differs greatly among cultivars of the same species. Increases in UV-B radiation resulting from stratospheric ozone depletion could alter productivity in some species, as shown in field studies with soybean and loblolly pine. However, in order to assess the magnitude of such changes, we must further understand the mechanisms of UV-B protection in tolerant species and damage in sensitive species as well as the potential indirect effects such as changes in competitive interactions or ecosystem processes

  14. The potential importance of frost flowers, recycling on snow, and open leads for ozone depletion events

    Directory of Open Access Journals (Sweden)

    M. Piot

    2008-05-01

    Full Text Available We present model studies with the one-dimensional model MISTRA to investigate the potential role of frost flowers, recycling on snow, and open leads in the depletion of tropospheric ozone in the Arctic spring. In our model, we assumed frost flower aerosols to be the major source of bromine. We show that a major ozone depletion event can be satisfactorily reproduced only if the recycling on snow of deposited bromine into gas phase bromine is assumed. In the model, this cycling is more efficient than the bromine explosion process and maintains sufficiently high levels of bromine to deplete ozone down to few nmol mol−1 within four days. We assessed the influence of different surface combinations (open lead/frost flowers on the chemistry in the model. Results showed noticeable modifications affecting the composition of aerosols and the deposition velocities. A model run with a series of coupled frost flower fields and open leads, separated by large areas of snow, showed results comparable with field observations. In addition, we studied the effects of modified temperature of either the frost flower field or the ambient airmass. A warmer frost flower field increases the relative humidity and the aerosol deposition rate. The deposition/re-emission process gains in importance, inducing more reactive bromine in the gas phase, and a stronger ozone depletion. A decrease of 1K in airmass temperature shows in our model that the aerosol uptake capacities of all gas phase species substantially increases, leading to enhanced uptake of acids from the gas phase. Consequently, the so-called bromine explosion accelerated and O3 mixing ratios decreased. In our model representation, variations in wind speed affected the aerosol source function and influenced the amount of bromine in the atmosphere and thus the ozone depletion strength. Recent studies have suggested the important role of the precipitation of calcium carbonate (CaCO3

  15. Environment and health: 3. Ozone depletion and ultraviolet radiation

    International Nuclear Information System (INIS)

    De Gruijl, F.R.; Van der Leun, J.C.

    2000-01-01

    Ultraviolet radiation from the sun is responsible for a variety of familiar photochemical reactions, including photochemical smog, bleaching of paints and decay of plastics. Conjugated bonds in organic molecules such as proteins and DNA absorb the UV radiation, which can damage these molecules. By a fortunate evolutionary event, the oxygen produced by photosynthesis forms a filter in the outer reaches of our atmosphere that absorbs the most energetic and harmful UV radiation, with wavelengths below 240 nm (in the UVC band [wavelength 100-280 nm]). In the process, the oxygen molecules split up and recombine to form ozone (Fig. 1). This ratified ozone layer (spread out between 10 and 50 Ion in the stratosphere but only 3 mm thick were it compressed at ground level) in turn efficiently absorbs UV radiation of higher wavelengths (tip to about 310 nm). A part of the UV radiation in the UVB band (wavelength 280-315 nm) still reaches ground level and is absorbed in sufficient amounts to have deleterious effects on cells. The less energetic radiation in the UVA band (wavelength 315-400 nm, bordering the visible band [wavelength 400-800 nm]) is not absorbed by ozone and reaches ground level without much attenuation through a clear atmosphere (i.e., no clouds, no air pollution). Although not completely innocuous, the UVA radiation in sunlight is much less photochemically active and therefore generally less harmful than UVB radiation. Life on earth has adapted itself to the UV stress, particularly UVB stress, fbr example by forming protective UV-absorbing surface layers, by repairing cell damage or by replacing damaged cells entirely. Human skin shows all of these adaptive features. Our eyes are less well adapted, but dicy, are shielded by the brows and by squinting. (author)

  16. Automotive industry program and strategy for control of ozone depleting substances and greenhouse gases

    International Nuclear Information System (INIS)

    Pound, F.R.; Stirling, P.J.

    1990-01-01

    This paper outlines the program status and strategy for the short and long term periods for ozone depleting substances and greenhouse gases from both stationary sources in manufacturing plants and mobile sources in motor vehicles. 5 refs

  17. Presence of stratospheric humidity in the ozone column depletion on the west coast of South America

    International Nuclear Information System (INIS)

    Da Silva, M. Luis; Gutierrez, O. Luis; Morales, S. Luis; Universidad de Chile, Santiago; Torres, C. Arnaldo

    2006-01-01

    The ozone column depletion over the western coast of South America has been previously explained, based on the existence of winds in the area of the depletion, which cause compression and thinning of the ozone layer. However, the presence of humidity and methane transported by these winds to the stratosphere where the ozone depletion is present gives evidence that these compounds also participate in the depletion of the ozone layer. These two compounds, humidity and methane, are analysed during the ozone depletion of January, 1998. It is observed that when humidity presents fluctuations, ozone has fluctuations too. A maximum of humidity corresponds to a minimum of ozone, but there is a shift in altitude between them. This shift is observed in the stratosphere and upper troposphere and corresponds to approximately 500 m. It is important to point out that during this event El Nino was present and the sources of methane are the Amazon forest and the Pacific Ocean. The data for this study was obtained from NASA and HALOE

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

    Science.gov (United States)

    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…

  19. Sensitivity of the Reaction Mechanism of the Ozone Depletion Events during the Arctic Spring on the Initial Atmospheric Composition of the Troposphere

    Directory of Open Access Journals (Sweden)

    Le Cao

    2016-09-01

    Full Text Available Ozone depletion events (ODEs during the Arctic spring have been investigated since the 1980s. It was found that the depletion of ozone is highly associated with the release of halogens, especially bromine containing compounds. These compounds originate from various substrates such as the ice/snow-covered surfaces in Arctic. In the present study, the dependence of the mixing ratios of ozone and principal bromine species during ODEs on the initial composition of the Arctic atmospheric boundary layer was investigated by using a concentration sensitivity analysis. This analysis was performed by implementing a reaction mechanism representing the ozone depletion and halogen release in the box model KINAL (KInetic aNALysis of reaction mechanics. The ratios between the relative change of the mixing ratios of particular species such as ozone and the variation in the initial concentration of each atmospheric component were calculated, which indicate the relative importance of each initial species in the chemical kinetic system. The results of the computations show that the impact of various chemical species is different for ozone and bromine containing compounds during the depletion of ozone. It was found that CH3CHO critically controls the time scale of the complete removal of ozone. However, the rate of the ozone loss and the maximum values of bromine species are only slightly influenced by the initial value of CH3CHO. In addition, according to the concentration sensitivity analysis, the reduction of initial Br2 was found to cause a significant retardant of the ODE while the initial mixing ratio of HBr exerts minor influence on both ozone and bromine species. In addition, it is also interesting to note that the increase of C2H2 would significantly raise the amount of HOBr and Br in the atmosphere while the ozone depletion is hardly changed.

  20. Dependence of model-simulated response to ozone depletion on stratospheric polar vortex climatology

    Science.gov (United States)

    Lin, Pu; Paynter, David; Polvani, Lorenzo; Correa, Gustavo J. P.; Ming, Yi; Ramaswamy, V.

    2017-06-01

    We contrast the responses to ozone depletion in two climate models: Community Atmospheric Model version 3 (CAM3) and Geophysical Fuild Dynamics Laboratory (GFDL) AM3. Although both models are forced with identical ozone concentration changes, the stratospheric cooling simulated in CAM3 is 30% stronger than in AM3 in annual mean, and twice as strong in December. We find that this difference originates from the dynamical response to ozone depletion, and its strength can be linked to the timing of the climatological springtime polar vortex breakdown. This mechanism is further supported by a variant of the AM3 simulation in which the southern stratospheric zonal wind climatology is nudged to be CAM3-like. Given that the delayed breakdown of the southern polar vortex is a common bias among many climate models, previous model-based assessments of the forced responses to ozone depletion may have been somewhat overestimated.

  1. The potential for ozone depletion in the Arctic polar stratosphere

    Energy Technology Data Exchange (ETDEWEB)

    Brune, W.H. (Pennsylvania State Univ., University Park (United States)); Anderson, J.G.; Toohey, D.W. (Harvard Univ., Cambridge, MA (United States)); Fahey, D.W.; Kawa, S.R. (National Oceanic and Atmospheric Administration, Boulder, CO (United States)); Jones, R.L. (Univ. of Cambridge (England)); McKenna, D.S. (United Kingdom Meteorological Office, Berkshire (England)); Poole, L.R. (NASA Langley Research Center, Hampton, VA (United States))

    1991-05-31

    The nature of the Arctic polar stratosphere is observed to be similar in many respects to that of the Antarctic polar stratosphere, where an ozone hole has been identified. most of the available chlorine (HCl and ClONO{sub 2}) was converted by reactions on polar stratospheric clouds to reactive ClO and Cl{sub 2}O{sub 2} throughout the Arctic polar vortex before midwinter. Reactive nitrogen was converted to HNO{sub 3}, and some, with spatial inhomogeneity, fell out of the stratosphere. These chemical changes ensured characteristic ozone losses of 10 to 15% at altitudes inside the polar vortex where polar stratospheric clouds had occurred. These local losses can translate into 5 to 8% losses in the vertical column abundance of ozone. As the amount of stratospheric chlorine inevitably increases by 50% over the next two decades, ozone losses recognizable as an ozone hole may well appear.

  2. A One-Dimensional Model Study of the Occurrence and the Termination of Polar Boundary-Layer Ozone Depletion Events

    Science.gov (United States)

    Cao, Le; Gutheil, Eva

    2015-04-01

    The tropospheric ozone depletion events (ODEs) in polar spring have attracted increased attention in the last thirty years. A dramatic decline of the surface ozone mixing ratio from tens of parts per billion (ppb) to less than one ppb within a few days is observed in various observation sites in polar regions. Previous studies suggest that the halogen species, especially bromine, acts as a catalyst in a chemical reaction cycle, which causes the destruction of ozone in the polar boundary layer. Moreover, a group of heterogeneous reactions with the involvement of HOBr occur on the surface of different substrates such as suspended aerosols and sea ice, leading to the activation of bromide from these substrates, and a following enhancement of the total bromine amount in the boundary layer occurs. This phenomenon is widely known as the 'bromine explosion' mechanism. However, the initiation and the termination steps of the ODEs are still not well understood. In the present study, a one-dimensional model, KINAL-T, is developed with the aim of investigating the role of the boundary layer in the occurrence and the termination of the ODEs. The 1-D model is an extension of the previous box model study1, explicitly including the vertical convection of gas. The parameterization of the vertical profile of the turbulent diffusivity from Pielke and Mahrer (1975)2 is adopted. Moreover, in the 1-D model, a bromine-related reaction scheme taken from Cao et al. (2014)1 is used, in which not only the gas phase but also the heterogeneous reactions are implemented. The simulation results show that the tropospheric ozone depletion event in a 200 m boundary layer starts after 12 days under the condition of a potential temperature gradient of 0.7 K km-1 and a wind speed of 5 m s-1. The whole depletion process of ozone takes approximately 2.5 days. The vertical profiles of ozone and bromine-containing compounds at different days are also captured. Instead of preventing the ozone from the

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

    Science.gov (United States)

    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

  4. Biological UV-doses and the effect on an ozone layer depletion

    International Nuclear Information System (INIS)

    Dahlback, A.; Henriksen, T.

    1988-08-01

    Effective UV-doses were calculated based on the integrated product of the biological action spectrum and the solar radiation. The calculations included absorption and scattering of UV-radiation in the atmosphere, both for normal ozone conditions as well as for a depleted ozone layer. The effective annual UV-dose increases by approximately 4% per degree of latitude towards the equator. An ozone depletion of 1% increases the annual UV-dose by approximately 1% at 60 o N. A large depletion of 50% over Scandinavia (60 o N) would give this region an effective UV-dose similar to that obtained, with normal ozone conditions, at a latitude of 40 o N (California or the Mediterranean countries). The Antarctic ozone hole increases the annual UV-dose by 20 to 25% which is a similar increase as that attained by moving 5 to 6 degrees of latitude nearer the equator. The annual UV-dose on higher latitudes is mainly determined by the summer values of ozone. Both the ozone values and the effective UV-doses vary from one year to another (within ±4%). No positive or negative trend is observed for Scandinavia from 1978 to 1988

  5. Ozone Depletion in Tropospheric Volcanic Plumes: From Halogen-Poor to Halogen-Rich Emissions

    Directory of Open Access Journals (Sweden)

    Tjarda J. Roberts

    2018-02-01

    Full Text Available Volcanic halogen emissions to the troposphere undergo a rapid plume chemistry that destroys ozone. Quantifying the impact of volcanic halogens on tropospheric ozone is challenging, only a few observations exist. This study presents measurements of ozone in volcanic plumes from Kīlauea (HI, USA, a low halogen emitter. The results are combined with published data from high halogen emitters (Mt Etna, Italy; Mt Redoubt, AK, USA to identify controls on plume processes. Ozone was measured during periods of relatively sustained Kīlauea plume exposure, using an Aeroqual instrument deployed alongside Multi-Gas SO2 and H2S sensors. Interferences were accounted for in data post-processing. The volcanic H2S/SO2 molar ratio was quantified as 0.03. At Halema‘uma‘u crater-rim, ozone was close to ambient in the emission plume (at 10 ppmv SO2. Measurements in grounding plume (at 5 ppmv SO2 about 10 km downwind of Pu‘u ‘Ō‘ō showed just slight ozone depletion. These Kīlauea observations contrast with substantial ozone depletion reported at Mt Etna and Mt Redoubt. Analysis of the combined data from these three volcanoes identifies the emitted Br/S as a strong but non-linear control on the rate of ozone depletion. Model simulations of the volcanic plume chemistry highlight that the proportion of HBr converted into reactive bromine is a key control on the efficiency of ozone depletion. This underlines the importance of chemistry in the very near-source plume on the fate and atmospheric impacts of volcanic emissions to the troposphere.

  6. Simulation of Halocarbon Production and Emissions and Effects on Ozone Depletion

    Science.gov (United States)

    Holmes; Ellis

    1997-09-01

    / This paper describes an integrated model that simulates future halocarbon production/emissions and potential ozone depletion. Applications and historical production levels for various halocarbons are discussed first. A framework is then presented for modeling future halocarbon impacts incorporating differences in underlying demands, applications, regulatory mandates, and environmental characteristics. The model is used to simulate the potential impacts of several prominent issues relating to halocarbon production, regulation, and environmental interactions, notably: changes in agricultural methyl bromide use, increases in effectiveness of bromine for ozone depletion, modifications to the elimination schedule for HCFCs, short-term expansion of CFC demand in low use compliance countries, and delays in Russian Federation compliance. Individually, each issue does not unequivocally represent a significant likely increase in long-term atmospheric halogen loading and stratospheric ozone depletion. In combination, however, these impacts could increase peak halogen concentrations and long-term integral halogen loading, resulting in higher levels of stratospheric ozone depletion and longer exposure to increased levels of UV radiation.KEY WORDS: Halocarbons; Ozone depletion; Montreal Protocol; Integrated assessment

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

    Science.gov (United States)

    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.

  8. Destruction of ozone-depleting substances in a thermal plasma reactor

    Science.gov (United States)

    Murphy, A. B.; McAllister, T.

    1998-07-01

    A two-dimensional numerical model of the PLASCON™ plasma reactor is used to investigate the destruction of ozone-depleting substances in the reactor. The model includes electromagnetic, fluid dynamic and chemical kinetic phenomena. Calculated temperature, flow and species concentration fields within the plasma torch, the injection manifold and the reaction tube are presented for the case of the destruction of CFC-12 (CF2Cl2). Conversion of CFC-12 to CFC-13 (CF3Cl), a more stable ozone-depleting substance, is found to occur in the region close to the injection manifold, and to be unaffected by reaction tube geometry. CFC-13 is predicted to be the dominant ozone-depleting substance in the exhaust gas. The predictions of the model are found to be in good agreement with measurements of the exhaust gas composition.

  9. Effect of odd hydrogen on ozone depletion by chlorine reactions

    Science.gov (United States)

    Donahue, T. M.; Cicerone, R. J.; Liu, S. C.; Chameides, W. L.

    1976-01-01

    The present paper discusses how the shape of the ozone layer changes under the influence of injected ClX for several choices of two key HOx reaction rates. The two HOx reactions are: OH + HO2 yields H2O + O2 and O + HO2 yields OH + O2. Results of calculations are presented which show that the two reaction rates determine the stratospheric concentrations of OH and HO2, and that these concentrations regulate the amount by which the stratospheric ozone column can be reduced due to injections of odd chlorine. It is concluded that the amount of ozone reduction by a given mixing ratio of ClX will remain very uncertain until the significance of several possible feedback effects involving HOx in a chlorine-polluted atmosphere are determined and measurements of the reaction rates and HOx concentrations are made at the relevant temperatures.

  10. Observing the Impact of Calbuco Volcanic Aerosols on South Polar Ozone Depletion in 2015

    OpenAIRE

    Stone, KA; Solomon, S; Kinnison, DE; Pitts, MC; Poole, LR; Mills, MJ; Schmidt, Anja; Neely, RR; Ivy, D; Schwartz, MJ; Vernier, JP; Johnson, BJ; Tully, MB; Klekociuk, AR; König-Langlo, G

    2017-01-01

    The Southern Hemisphere Antarctic stratosphere experienced two noteworthy events in 2015: a significant injection of sulfur from the Calbuco volcanic eruption in Chile in April and a record-large Antarctic ozone hole in October and November. Here we quantify Calbuco's influence on stratospheric ozone depletion in austral spring 2015 using observations and an Earth system model. We analyze ozonesondes, as well as data from the Microwave Limb Sounder. We employ the Community Earth System Model,...

  11. Ultraviolet radiation affects emission of ozone-depleting substances by marine macroalgae: results from a laboratory incubation study.

    Science.gov (United States)

    Laturnus, Frank; Svensson, Teresia; Wiencke, Christian; Oberg, Gunilla

    2004-12-15

    The depletion of stratospheric ozone due to the effects of ozone-depleting substances, such as volatile organohalogens, emitted into the atmosphere from industrial and natural sources has increased the amount of ultraviolet radiation reaching the earth's surface. Especially in the subpolar and polar regions, where stratospheric ozone destruction is the highest, individual organisms and whole ecosystems can be affected. In a laboratory study, several species of marine macroalgae occurring in the polar and northern temperate regions were exposed to elevated levels of ultraviolet radiation. Most of the macroalgae released significantly more chloroform, bromoform, dibromomethane, and methyl iodide-all volatile organohalogens. Calculating on the basis of the release of total chlorine, bromine, and iodine revealed that, except for two macroalgae emitting chlorine and one alga emitting iodine, exposure to ultraviolet radiation caused macroalgae to emit significantly more total chlorine, bromine, and iodine. Increasing levels of ultraviolet radiation due to possible further destruction of the stratospheric ozone layer as a result of ongoing global atmospheric warming may thus increase the future importance of marine macroalgae as a source for the global occurrence of reactive halogen-containing compounds.

  12. Effect of pesticides on surface ozone concentration

    International Nuclear Information System (INIS)

    Farag, S.A.; Rizk, H.F.S.; Elbahnasawy, R.M.; Meleigy, M.I.

    1992-01-01

    A comparative study through seasonal variation of surface ozone concentration was carried out recently (1991-1992) at a background area free from expected urban pollutants (Shebin ElKom) and industrial and urban areas (Cairo). Surface ozone concentrations in ppb were generally lower in such area compared with urban or industrial areas studied through the comparative seasonal variations. Notable smog values (>100 ppb) of hourly surface ozone concentrations appeared during summer season in this rural area; during this season, some pesticides were sprayed over cotton and other crops fields in near by agricultural areas. The unexpected jump in the values of diurnal concentrations of surface ozone in that area may be due to the photochemical reactions of these organic pesticides in the atmosphere. 1 fig, 3 tab

  13. Observing the Impact of Calbuco Volcanic Aerosols on South Polar Ozone Depletion in 2015

    Science.gov (United States)

    Stone, Kane A.; Solomon, Susan; Kinnison, Doug E.; Pitts, Michael C.; Poole, Lamont R.; Mills, Michael J.; Schmidt, Anja; Neely, Ryan R.; Ivy, Diane; Schwartz, Michael J.; Vernier, Jean-Paul; Johnson, Bryan J.; Tully, Matthew B.; Klekociuk, Andrew R.; König-Langlo, Gert; Hagiya, Satoshi

    2017-11-01

    The Southern Hemisphere Antarctic stratosphere experienced two noteworthy events in 2015: a significant injection of sulfur from the Calbuco volcanic eruption in Chile in April and a record-large Antarctic ozone hole in October and November. Here we quantify Calbuco's influence on stratospheric ozone depletion in austral spring 2015 using observations and an Earth system model. We analyze ozonesondes, as well as data from the Microwave Limb Sounder. We employ the Community Earth System Model, version 1, with the Whole Atmosphere Community Climate Model (WACCM) in a specified dynamics setup, which includes calculations of volcanic effects. The Cloud-Aerosol Lidar with Orthogonal Polarization data indicate enhanced volcanic liquid sulfate 532 nm backscatter values as far poleward as 68°S during October and November (in broad agreement with WACCM). Comparison of the location of the enhanced aerosols to ozone data supports the view that aerosols played a major role in increasing the ozone hole size, especially at pressure levels between 150 and 100 hPa. Ozonesonde vertical ozone profiles from the sites of Syowa, South Pole, and Neumayer display the lowest individual October or November measurements at 150 hPa since the 1991 Mount Pinatubo eruption period, with Davis showing similarly low values, but no available 1990 data. The analysis suggests that under the cold conditions ideal for ozone depletion, stratospheric volcanic aerosol particles from the moderate-magnitude eruption of Calbuco in 2015 greatly enhanced austral ozone depletion, particularly at 55-68°S, where liquid binary sulfate aerosols have a large influence on ozone concentrations.

  14. Persistent polar depletion of stratospheric ozone and emergent mechanisms of ultraviolet radiation-mediated health dysregulation.

    Science.gov (United States)

    Dugo, Mark A; Han, Fengxiang; Tchounwou, Paul B

    2012-01-01

    Year 2011 noted the first definable ozone "hole" in the Arctic region, serving as an indicator to the continued threat of dangerous ultraviolet radiation (UVR) exposure caused by the deterioration of stratospheric ozone in the northern hemisphere. Despite mandates of the Montreal Protocol to phase out the production of ozone-depleting chemicals (ODCs), the relative stability of ODCs validates popular notions of persistent stratospheric ozone for several decades. Moreover, increased UVR exposure through stratospheric ozone depletion is occurring within a larger context of physiologic stress and climate change across the biosphere. In this review, we provide commentaries on stratospheric ozone depletion with relative comparisons between the well-known Antarctic ozone hole and the newly defined ozone hole in the Arctic. Compared with the Antarctic region, the increased UVR exposure in the Northern Hemisphere poses a threat to denser human populations across North America, Europe, and Asia. In this context, we discuss emerging targets of UVR exposure that can potentially offset normal biologic rhythms in terms of taxonomically conserved photoperiod-dependent seasonal signaling and entrainment of circadian clocks. Consequences of seasonal shifts during critical life history stages can alter fitness and condition, whereas circadian disruption is increasingly becoming associated as a causal link to increased carcinogenesis. We further review the significance of genomic alterations via UVR-induced modulations of phase I and II transcription factors located in skin cells, the aryl hydrocarbon receptor (AhR), and the nuclear factor (erythroid-derived 2)-related factor 2 (Nrf2), with emphasis on mechanism that can lead to metabolic shifts and cancer. Although concern for adverse health consequences due to increased UVR exposure are longstanding, recent advances in biochemical research suggest that AhR and Nrf2 transcriptional regulators are likely targets for UVR

  15. 21 CFR 2.125 - Use of ozone-depleting substances in foods, drugs, devices, or cosmetics.

    Science.gov (United States)

    2010-04-01

    ..., devices, or cosmetics. 2.125 Section 2.125 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF... Specific Products Subject to the Federal Food, Drug, and Cosmetic Act § 2.125 Use of ozone-depleting substances in foods, drugs, devices, or cosmetics. (a) As used in this section, ozone-depleting substance...

  16. The human health effects of ozone depletion and interactions with climate change.

    Science.gov (United States)

    Norval, M; Lucas, R M; Cullen, A P; de Gruijl, F R; Longstreth, J; Takizawa, Y; van der Leun, J C

    2011-02-01

    Depletion of the stratospheric ozone layer has led to increased solar UV-B radiation (280-315 nm) at the surface of the Earth. This change is likely to have had an impact on human exposure to UV-B radiation with consequential detrimental and beneficial effects on health, although behavioural changes in society over the past 60 years or so with regard to sun exposure are of considerable importance. The present report concentrates on information published since our previous report in 2007. The adverse effects of UV radiation are primarily on the eye and the skin. While solar UV radiation is a recognised risk factor for some types of cataract and for pterygium, the evidence is less strong, although increasing, for ocular melanoma, and is equivocal at present for age-related macular degeneration. For the skin, the most common harmful outcome is skin cancer, including melanoma and the non-melanoma skin cancers, basal cell carcinoma and squamous cell carcinoma. The incidence of all three of these tumours has risen significantly over the past five decades, particularly in people with fair skin, and is projected to continue to increase, thus posing a significant world-wide health burden. Overexposure to the sun is the major identified environmental risk factor in skin cancer, in association with various genetic risk factors and immune effects. Suppression of some aspects of immunity follows exposure to UV radiation and the consequences of this modulation for the immune control of infectious diseases, for vaccination and for tumours, are additional concerns. In a common sun allergy (polymorphic light eruption), there is an imbalance in the immune response to UV radiation, resulting in a sun-evoked rash. The major health benefit of exposure to solar UV-B radiation is the production of vitamin D. Vitamin D plays a crucial role in bone metabolism and is also implicated in protection against a wide range of diseases. Although there is some evidence supporting protective effects

  17. Ozone Depletion at Mid-Latitudes: Coupling of Volcanic Aerosols and Temperature Variability to Anthropogenic Chlorine

    Science.gov (United States)

    Solomon, S.; Portmann, R. W.; Garcia, R. R.; Randel, W.; Wu, F.; Nagatani, R.; Gleason, J.; Thomason, L.; Poole, L. R.; McCormick, M. P.

    1998-01-01

    Satellite observations of total ozone at 40-60 deg N are presented from a variety of instruments over the time period 1979-1997. These reveal record low values in 1992-3 (after Pinatubo) followed by partial but incomplete recovery. The largest post-Pinatubo reductions and longer-term trends occur in spring, providing a critical test for chemical theories of ozone depletion. The observations are shown to be consistent with current understanding of the chemistry of ozone depletion when changes in reactive chlorine and stratospheric aerosol abundances are considered along with estimates of wave-driven fluctuations in stratospheric temperatures derived from global temperature analyses. Temperature fluctuations are shown to make significant contributions to model calculated northern mid-latitude ozone depletion due to heterogeneous chlorine activation on liquid sulfate aerosols at temperatures near 200-210 K (depending upon water vapor pressure), particularly after major volcanic eruptions. Future mid-latitude ozone recovery will hence depend not only on chlorine recovery but also on temperature trends and/or variability, volcanic activity, and any trends in stratospheric sulfate aerosol.

  18. Ozone Depleting Chemical (ODC) Replacement - Alternative Cleaning Solvents and Lubricants.

    Science.gov (United States)

    1995-02-01

    propylene carbonate and d- limonene ) cleaned better than the existing TCA. This project was demonstrative in not only eliminating chemicals known to deplete...34* Compatible with propellants. "* Compliant with safety and environmental requirements. "* Meets minimum cleanliness requirements of governing...compatibility, propellant compatibility, and low residue upon cleaner removal. In addition, the use of the cleaner should not impose any safety or

  19. Simulation of ozone depletion using ambient irradiance supplemented with UV lamps.

    Science.gov (United States)

    Díaz, S; Camilión, C; Escobar, J; Deferrari, G; Roy, S; Lacoste, K; Demers, S; Belzile, C; Ferreyra, G; Gianesella, S; Gosselin, M; Nozais, C; Pelletier, E; Schloss, I; Vernet, M

    2006-01-01

    In studies of the biological effects of UV radiation, ozone depletion can be mimicked by performing the study under ambient conditions and adding radiation with UV-B lamps. We evaluated this methodology at three different locations along a latitudinal gradient: Rimouski (Canada), Ubatuba (Brazil) and Ushuaia (Argentina). Experiments of the effect of potential ozone depletion on marine ecosystems were carried out in large outdoor enclosures (mesocosms). In all locations we simulated irradiances corresponding to 60% ozone depletion, which may produce a 130-1900% increase in 305 nm irradiance at noon, depending on site and season. Supplementation with a fixed percentage of ambient irradiance provides a better simulation of irradiance increase due to ozone depletion than supplementation with a fixed irradiance value, particularly near sunrise and sunset or under cloudy skies. Calculations performed for Ushuaia showed that, on very cloudy days, supplementation by the square-wave method may produce unrealistic irradiances. Differences between the spectra of the calculated supplementing irradiance and the lamp for a given site and date will be a function of the time of day and may become more or less pronounced according to the biological weighting function of the effect under study.

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

    Science.gov (United States)

    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…

  1. Decline in Antarctic Ozone Depletion and Lower Stratospheric Chlorine Determined From Aura Microwave Limb Sounder Observations

    Science.gov (United States)

    Strahan, Susan E.; Douglass, Anne R.

    2018-01-01

    Attribution of Antarctic ozone recovery to the Montreal protocol requires evidence that (1) Antarctic chlorine levels are declining and (2) there is a reduction in ozone depletion in response to a chlorine decline. We use Aura Microwave Limb Sounder measurements of O3, HCl, and N2O to demonstrate that inorganic chlorine (Cly) from 2013 to 2016 was 223 ± 93 parts per trillion lower in the Antarctic lower stratosphere than from 2004 to 2007 and that column ozone depletion declined in response. The mean Cly decline rate, 0.8%/yr, agrees with the expected rate based on chlorofluorocarbon lifetimes. N2O measurements are crucial for identifying changes in stratospheric Cly loading independent of dynamical variability. From 2005 to 2016, the ozone depletion and Cly time series show matching periods of decline, stability, and increase. The observed sensitivity of O3 depletion to changing Cly agrees with the sensitivity simulated by the Global Modeling Initiative chemistry transport model integrated with Modern Era Retrospective Analysis for Research and Applications 2 meteorology.

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

    Science.gov (United States)

    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…

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

    Science.gov (United States)

    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)

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

    Science.gov (United States)

    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)

  5. Improvements in Total Column Ozone in GEOSCCM and Comparisons with a New Ozone-Depleting Substances Scenario

    Science.gov (United States)

    Oman, Luke D.; Douglass, Anne R.

    2014-01-01

    The evolution of ozone is examined in the latest version of the Goddard Earth Observing System Chemistry-Climate Model (GEOSCCM) using old and new ozone-depleting substances (ODS) scenarios. This version of GEOSCCM includes a representation of the quasi-biennial oscillation, a more realistic implementation of ozone chemistry at high solar zenith angles, an improved air/sea roughness parameterization, and an extra 5 parts per trillion of CH3Br to account for brominated very short-lived substances. Together these additions improve the representation of ozone compared to observations. This improved version of GEOSCCM was used to simulate the ozone evolution for the A1 2010 and the newStratosphere-troposphere Processes and their Role in Climate (SPARC) 2013 ODS scenario derived using the SPARC Lifetimes Report 2013. This new ODS scenario results in a maximum Cltot increase of 65 parts per trillion by volume (pptv), decreasing slightly to 60 pptv by 2100. Approximately 72% of the increase is due to the longer lifetime of CFC-11. The quasi-global (60degS-60degN) total column ozone difference is relatively small and less than 1Dobson unit on average and consistent with the 3-4% larger 2050-2080 average Cly in the new SPARC 2013 scenario. Over high latitudes, this small change in Cly compared to the relatively large natural variabilitymakes it not possible to discern a significant impact on ozone in the second half of the 21st century in a single set of simulations.

  6. The consequences for human health of stratospheric ozone depletion in association with other environmental factors.

    Science.gov (United States)

    Lucas, R M; Norval, M; Neale, R E; Young, A R; de Gruijl, F R; Takizawa, Y; van der Leun, J C

    2015-01-01

    Due to the implementation of the Montreal Protocol, which has limited, and is now probably reversing, the depletion of the stratospheric ozone layer, only modest increases in solar UV-B radiation at the surface of the Earth have occurred. For many fair-skinned populations, changing behaviour with regard to exposure to the sun over the past half century - more time in the sun, less clothing cover (more skin exposed), and preference for a tan - has probably contributed more to greater levels of exposure to UV-B radiation than ozone depletion. Exposure to UV-B radiation has both adverse and beneficial effects on human health. This report focuses on an assessment of the evidence regarding these outcomes that has been published since our previous report in 2010. The skin and eyes are the organs exposed to solar UV radiation. Excessive solar irradiation causes skin cancer, including cutaneous malignant melanoma and the non-melanoma skin cancers, basal cell carcinoma and squamous cell carcinoma, and contributes to the development of other rare skin cancers such as Merkel cell carcinoma. Although the incidence of melanoma continues to increase in many countries, in some locations, primarily those with strong sun protection programmes, incidence has stabilised or decreased over the past 5 years, particularly in younger age-groups. However, the incidence of non-melanoma skin cancers is still increasing in most locations. Exposure of the skin to the sun also induces systemic immune suppression that may have adverse effects on health, such as through the reactivation of latent viral infections, but also beneficial effects through suppression of autoimmune reactivity. Solar UV-B radiation damages the eyes, causing cataracts and pterygium. UV-B irradiation of the skin is the main source of vitamin D in many geographic locations. Vitamin D plays a critical role in the maintenance of calcium homeostasis in the body; severe deficiency causes the bone diseases, rickets in children

  7. A quantitative analysis of the reactions involved in stratospheric ozone depletion in the polar vortex core

    Science.gov (United States)

    Wohltmann, Ingo; Lehmann, Ralph; Rex, Markus

    2017-09-01

    We present a quantitative analysis of the chemical reactions involved in polar ozone depletion in the stratosphere and of the relevant reaction pathways and cycles. While the reactions involved in polar ozone depletion are well known, quantitative estimates of the importance of individual reactions or reaction cycles are rare. In particular, there is no comprehensive and quantitative study of the reaction rates and cycles averaged over the polar vortex under conditions of heterogeneous chemistry so far. We show time series of reaction rates averaged over the core of the polar vortex in winter and spring for all relevant reactions and indicate which reaction pathways and cycles are responsible for the vortex-averaged net change of the key species involved in ozone depletion, i.e., ozone, chlorine species (ClOx, HCl, ClONO2), bromine species, nitrogen species (HNO3, NOx) and hydrogen species (HOx). For clarity, we focus on one Arctic winter (2004-2005) and one Antarctic winter (2006) in a layer in the lower stratosphere around 54 hPa and show results for additional pressure levels and winters in the Supplement. Mixing ratios and reaction rates are obtained from runs of the ATLAS Lagrangian chemistry and transport model (CTM) driven by the European Centre for Medium-Range Weather Forecasts (ECMWF) ERA-Interim reanalysis data. An emphasis is put on the partitioning of the relevant chemical families (nitrogen, hydrogen, chlorine, bromine and odd oxygen) and activation and deactivation of chlorine.

  8. A quantitative analysis of the reactions involved in stratospheric ozone depletion in the polar vortex core

    Directory of Open Access Journals (Sweden)

    I. Wohltmann

    2017-09-01

    Full Text Available We present a quantitative analysis of the chemical reactions involved in polar ozone depletion in the stratosphere and of the relevant reaction pathways and cycles. While the reactions involved in polar ozone depletion are well known, quantitative estimates of the importance of individual reactions or reaction cycles are rare. In particular, there is no comprehensive and quantitative study of the reaction rates and cycles averaged over the polar vortex under conditions of heterogeneous chemistry so far. We show time series of reaction rates averaged over the core of the polar vortex in winter and spring for all relevant reactions and indicate which reaction pathways and cycles are responsible for the vortex-averaged net change of the key species involved in ozone depletion, i.e., ozone, chlorine species (ClOx, HCl, ClONO2, bromine species, nitrogen species (HNO3, NOx and hydrogen species (HOx. For clarity, we focus on one Arctic winter (2004–2005 and one Antarctic winter (2006 in a layer in the lower stratosphere around 54 hPa and show results for additional pressure levels and winters in the Supplement. Mixing ratios and reaction rates are obtained from runs of the ATLAS Lagrangian chemistry and transport model (CTM driven by the European Centre for Medium-Range Weather Forecasts (ECMWF ERA-Interim reanalysis data. An emphasis is put on the partitioning of the relevant chemical families (nitrogen, hydrogen, chlorine, bromine and odd oxygen and activation and deactivation of chlorine.

  9. Experimental and theoretical investigation of stratospheric ozone depletion in the northern hemisphere caused by heterogeneous chemistry

    Science.gov (United States)

    Storvold, Rune

    Stratospheric ozone is of crucial importance for life on Earth. This thin layer protects us from the ultraviolet solar radiation and also works as a greenhouse gas that helps maintaining our climate. Large changes in thickness and vertical distribution of the ozone abundance may have detrimental effects on life on Earth. But even small changes could have considerable impact on UV irradiance, bio-production and cancer rates. During the last decade record low spring time vertical column amounts of stratospheric ozone have been observed over Northern Europe. However, this decrease is not as severe as the depletion observed over Antarctica and at mid-latitudes in the Southern Hemisphere. The discovery of the spring time stratospheric ozone depletion first in Antarctica and later in the Arctic has triggered international research efforts on stratospheric ozone chemistry and the possible effects of human activities on the ozone layer. Ground-based differential optical absorption spectroscopy measurements of NO2 and ozone have been performed over Fairbanks (65°N) and Ny-Ålesund (79°N) during the 1994-95 season. In this work we present improvements to ground based differential optical spectroscopy measurements by improving dark current corrections and spectral fitting of spectrographic photo diode array detector measurements. We have also improved the retrieval of vertical column amounts from diffuse light measurements by improving the corrections for seasonal changes in absorber air mass. This is particularly important at high latitudes. We used these data together with local weather and ozone sounding data, and with trace gas and aerosol data measured by other ground based instruments and by instruments deployed on satellites. This comprehensive dataset was used to investigate the performance of two current state of the art chemical transport models with and without the presence of heterogeneous chemistry. These are the University of Cambridge SLIMCAT model and the

  10. Characteristics of tropospheric ozone depletion events in the Arctic spring: analysis of the ARCTAS, ARCPAC, and ARCIONS measurements and satellite BrO observations

    Directory of Open Access Journals (Sweden)

    J.-H. Koo

    2012-10-01

    Full Text Available Arctic ozone depletion events (ODEs are caused by halogen catalyzed ozone loss. In situ chemistry, advection of ozone-poor air mass, and vertical mixing in the lower troposphere are important factors affecting ODEs. To better characterize the ODEs, we analyze the combined set of surface, ozonesonde, and aircraft in situ measurements of ozone and bromine compounds during the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS, the Aerosol, Radiation, and Cloud Processes affecting Arctic Climate (ARCPAC, and the Arctic Intensive Ozonesonde Network Study (ARCIONS experiments (April 2008. Tropospheric BrO columns retrieved from satellite measurements and back trajectory calculations are also used to investigate the characteristics of observed ODEs. In situ observations from these field experiments are inadequate to validate tropospheric BrO columns derived from satellite measurements. In view of this difficulty, we construct an ensemble of tropospheric column BrO estimates from two satellite (OMI and GOME-2 measurements and with three independent methods of calculating stratospheric BrO columns. Furthermore, we select analysis methods that do not depend on the absolute magnitude of column BrO, such as time-lagged correlation analysis of ozone and tropospheric column BrO, to understand characteristics of ODEs. Time-lagged correlation analysis between in situ (surface and ozonesonde measurements of ozone and satellite derived tropospheric BrO columns indicates that the ODEs are due to either local halogen-driven ozone loss or short-range (∼1 day transport from nearby regions with ozone depletion. The effect of in situ ozone loss is also evident in the diurnal variation difference between low (10th and 25th percentiles and higher percentiles of surface ozone concentrations at Alert, Canada. Aircraft observations indicate low-ozone air mass transported from adjacent high-BrO regions. Correlation analyses of ozone

  11. Nocturnal Ozone Depletion Events at the Amphitrite Point Observatory on West Vancouver Island

    Science.gov (United States)

    Garner, N.; Brownsey, D. K.; Tokarek, T. W.; Ye, C. Z.; Yordanov, N. R.; Osthoff, H. D.; Schiller, C. L.; Vingarzan, R.

    2015-12-01

    Routine monitoring stations on the West coast of North America serve to monitor baseline levels of criteria pollutants such as ozone (O3) arriving from the Pacific Ocean. In Canada, the Amphitrite Point Observatory (APO) in Ucluelet on the West coast of Vancouver Island has been added to this network to provide regional baseline measurements. Recently, McKendry and coworkers have reported frequent episodes of nocturnal O3 depletion events (ODEs) at APO (range: 5-20 ppbv) that generally correlate with alongshore winds, elevated levels of carbon dioxide (CO2), and low vertical entrainment but whose cause(s) has (have) remained unclear. In this work, results from the Ozone-depleting reactions in a coastal atmosphere (ORCA) campaign, which took place at APO from July 6 - 31, 2015, are presented. In addition to the long-term measurements that include aerosol size distribution and composition measurements, mixing ratios of speciated monoterpenes (e.g., α- and β-pinene, limonene), molecular halogens (i.e., Cl2, I2), halogen oxides (i.e., OIO), plus a full suite of nitrogen oxides (including N2O5, PAN, PPN, ΣPN, ΣAN, HNO3, HONO, and ClNO2) were quantified. Synoptic conditions at the site varied greatly between nights. During westerly flow of relatively clean marine air, O3 was generally conserved at night, indicating that deposition of O3 to the ocean surface is a minor loss pathway. When the air mass originated from other sectors, episodes of nocturnal ODEs were observed on several occasions, in which mixing ratios of biogenic VOCs were enhanced. These included air masses that originated from densely forested areas to the East, air masses polluted by marine traffic emissions from the southeast, and air masses from the NW that have traveled parallel to the coastline. In this sector, the air was likely in contact with terrestrial vegetation via land-sea breeze circulations. The results suggest that nocturnal ODEs at APO are mainly driven by local or regional processes

  12. An assessment of alternatives and technologies for replacing ozone- depleting substances at DOE facilities

    Energy Technology Data Exchange (ETDEWEB)

    Purcell, C.W.; Miller, K.B.; Friedman, J.R.; Rapoport, R.D.; Conover, D.R.; Hendrickson, P.L. [Pacific Northwest Lab., Richland, WA (United States); Koss, T.C. [USDOE Assistant Secretary for Environment, Safety, and Health, Washington, DC (United States). Office of Environmental Guidance

    1992-10-01

    Title VI of the Clean Air Act, as amended, mandates a production phase-out for ozone-depleting substances (ODSs). These requirements will have a significant impact on US Department of Energy (DOE) facilities. Currently, DOE uses ODSs in three major activities: fire suppression (halon), refrigeration and cooling (chlorofluorocarbons [CFCs]), and cleaning that requires solvents (CFCs, methyl chloroform, and carbon tetrachloride). This report provides basic information on methods and strategies to phase out use of ODSs at DOE facilities.

  13. Vertical structure of Antarctic tropospheric ozone depletion events: characteristics and broader implications

    Directory of Open Access Journals (Sweden)

    A. E. Jones

    2010-08-01

    Full Text Available The majority of tropospheric ozone depletion event (ODE studies have focussed on time-series measurements, with comparatively few studies of the vertical component. Those that exist have almost exclusively used free-flying balloon-borne ozonesondes and almost all have been conducted in the Arctic. Here we use measurements from two separate Antarctic field experiments to examine the vertical profile of ozone during Antarctic ODEs. We use tethersonde data to probe details in the lowest few hundred meters and find considerable structure in the profiles associated with complex atmospheric layering. The profiles were all measured at wind speeds less than 7 ms−1, and on each occasion the lowest inversion height lay between 10 m and 40 m. We also use data from a free-flying ozonesonde study to select events where ozone depletion was recorded at altitudes >1 km above ground level. Using ERA-40 meteorological charts, we find that on every occasion the high altitude depletion was preceded by an atmospheric low pressure system. An examination of limited published ozonesonde data from other Antarctic stations shows this to be a consistent feature. Given the link between BrO and ODEs, we also examine ground-based and satellite BrO measurements and find a strong association between atmospheric low pressure systems and enhanced BrO that must arise in the troposphere. The results suggest that, in Antarctica, such depressions are responsible for driving high altitude ODEs and for generating the large-scale BrO clouds observed from satellites. In the Arctic, the prevailing meteorology differs from that in Antarctica, but, while a less common effect, major low pressure systems in the Arctic can also generate BrO clouds. Such depressions thus appear to be fundamental when considering the broader influence of ODEs, certainly in Antarctica, such as halogen export and the radiative influence of ozone-depleted air masses.

  14. Halogens and their role in polar boundary-layer ozone depletion

    Directory of Open Access Journals (Sweden)

    W. R. Simpson

    2007-08-01

    Full Text Available During springtime in the polar regions, unique photochemistry converts inert halide salt ions (e.g. Br into reactive halogen species (e.g. Br atoms and BrO that deplete ozone in the boundary layer to near zero levels. Since their discovery in the late 1980s, research on ozone depletion events (ODEs has made great advances; however many key processes remain poorly understood. In this article we review the history, chemistry, dependence on environmental conditions, and impacts of ODEs. This research has shown the central role of bromine photochemistry, but how salts are transported from the ocean and are oxidized to become reactive halogen species in the air is still not fully understood. Halogens other than bromine (chlorine and iodine are also activated through incompletely understood mechanisms that are probably coupled to bromine chemistry. The main consequence of halogen activation is chemical destruction of ozone, which removes the primary precursor of atmospheric oxidation, and generation of reactive halogen atoms/oxides that become the primary oxidizing species. The different reactivity of halogens as compared to OH and ozone has broad impacts on atmospheric chemistry, including near complete removal and deposition of mercury, alteration of oxidation fates for organic gases, and export of bromine into the free troposphere. Recent changes in the climate of the Arctic and state of the Arctic sea ice cover are likely to have strong effects on halogen activation and ODEs; however, more research is needed to make meaningful predictions of these changes.

  15. Simulation of increasing UV radiation as a consequence of ozone depletion

    Science.gov (United States)

    Diaz, Susana B.; Camilion, Carolina; Lacoste, Karine; Escobar, Julio; Demers, Serge; Gianesella, Sonia M. F.; Roy, Suzanne

    2003-11-01

    UV plays a key roll in several biological functions. As consequence of the ozone depletion investigations to study the effects of UV radiation on human health and terrestrial and aquatic ecosystems have been carried out in laboratories and in the field. Experiments performed in laboratories, irradiating samples with lamps often present the inconvenience that light sources do not reproduce properly the solar spectrum. Field experiments are usually carried out comparing samples exposed to ambient irradiance (normal or increased) against 100% UV-B screened samples. This scenario also differs from the real situation of normal irradiance against UV-B increased irradiance. Some authors have solved this problem performing studies under ambient conditions, simulating the ozone depletion by supplementation of the UV-B radiation with lamps. As part of the IAI CNR-26, "Enhanced Ultraviolet-B Radiation in Natural Ecosystems as an added Perturbation due to Ozone Depletion," mesocosms experiments were performed at Rimouski, Canada), Ubatuba (Brasil) and Ushuaia, Argentina) using the supplementing methodology. In this paper we introduce the design of the measurements and lamps setting and the methodology used to calculate the attenuation constant and the irradiance at the water column at the mesocosms during the experiment, emphasizing on the Ubatuba campaign.

  16. Effect of climate change relative to ozone depletion on UV exposure in subarctic lakes.

    Science.gov (United States)

    Pienitz, R; Vincent, W F

    2000-03-30

    The effect of stratospheric ozone depletion on increases in ambient levels of solar ultraviolet (UV) radiation in high-latitude regions' has raised concerns about the response of northern ecosystems to environmental change. The concentration of coloured dissolved organic material, which is derived from terrestrial vegetation and acts as a screen for ultraviolet radiation, is low in high-latitude lakes. The underwater light environment in these lakes is therefore likely to be sensitive to small variations in the supply of this material, in addition to the effects of ozone depletion. Here we use fossil diatom assemblages in combination with bio-optical models to estimate the magnitude of past variations in the underwater light regime of a lake at the boreal tree line. We find large shifts in underwater UV-B, UV-A and photosynthetically available radiation associated with changes in the input of coloured dissolved organic material into subarctic lakes during the Holocene. The inferred changes in biological exposure to UV radiation were at least two orders of magnitude greater than those associated with moderate (30%) ozone depletion. Our findings indicate that freshwater ecosystems at present located across vegetation gradients will experience significant shifts in underwater spectral irradiance through the effects of climate change on catchment vegetation and the export of coloured dissolved organic material.

  17. Observations of depleted ozone within the boundary layer of the western North Atlantic

    Energy Technology Data Exchange (ETDEWEB)

    Berkowitz, C.M.; Busness, K.M.; Chapman, E.G. [Pacific Northwest Labs., Richland, WA (United States)] [and others

    1995-06-20

    Ozone measurements taken between 0.90 and 2.5 km above the surface and extending over an 800-km radius from Halifax, Nova Scotia, are presented from aircraft flights between August 21 and September 14, 1992. The mean ozone mixing ratio was found generally to be greater above the top of the mixed layer than near the sea surface. Eleven of the 32 vertical profiles displayed an abrupt transition at the top of the boundary layer, with surface ozone mixing ratios having values of {approx}15-20 ppb and values above the boundary layer increasing to {approx}50-60 ppb. This transition below low and high mixing ratios was observed to occur over a vertical scale of less than 0.5 km in surroundings taken within 4 hours of each other over horizontal distances of the order of several hundred kilometers. There was a well-mixed boundary layer in all cases where these sudden transitions in the ozone profiles were observed. These profiles are associated with subsidence over land, followed by dry deposition within a hydrocarbon-poor, well-mixed continental boundary layer. Ozone loss through surface deposition exceeded ozone production by the time the air masses arrived at the maritime coastal waters. Two other broad categories of profiles are described, the most common having the ozone mixing ratio increasing linearly with height to the top of the sampling domain at 2.5 km. A third category had only a local maximum in ozone with much smaller values higher and lower in the atmosphere. 26 refs., 11 figs., 3 tabs.

  18. 77 FR 74381 - Protection of Stratospheric Ozone: Listing of Substitutes for Ozone Depleting Substances-Fire...

    Science.gov (United States)

    2012-12-14

    ... Depleting Substances--Fire Suppression and Explosion Protection AGENCY: Environmental Protection Agency (EPA... published a direct final rule and a companion proposed rule issuing listings for three fire suppressants... three fire suppressants under EPA's Significant New Alternatives Policy program (77 FR 58035). Because...

  19. Depletion of stratospheric ozone over the Antarctic and Arctic : Responses of plants of polar terrestrial ecosystems to enhanced UV-B, an overview

    NARCIS (Netherlands)

    Rozema, Jelte; Boelen, Peter; Blokker, Peter

    2005-01-01

    Depletion of stratospheric ozone over the Antarctic has been re-occurring yearly since 1974, leading to enhanced UV-B radiation. Arctic ozone depletion has been observed since 1990. Ozone recovery has been predicted by 2050, but no signs of recovery occur. Here we review responses of polar plants to

  20. Depletion of stratospheric ozone over the Antarctic and Arctic: Responses of plants of polar terrestrial ecosystems to enhanced UV-B, an overview.

    NARCIS (Netherlands)

    Rozema, J.; Boelen, P.; Blokker, P.

    2005-01-01

    Depletion of stratospheric ozone over the Antarctic has been re-occurring yearly since 1974, leading to enhanced UV-B radiation. Arctic ozone depletion has been observed since 1990. Ozone recovery has been predicted by 2050, but no signs of recovery occur. Here we review responses of polar plants to

  1. Emission location dependent ozone depletion potentials for very short-lived halogenated species

    Directory of Open Access Journals (Sweden)

    I. Pisso

    2010-12-01

    Full Text Available We present trajectory-based estimates of Ozone Depletion Potentials (ODPs for very short-lived halogenated source gases as a function of surface emission location. The ODPs are determined by the fraction of source gas and its degradation products which reach the stratosphere, depending primarily on tropospheric transport and chemistry, and the effect of the resulting reactive halogen in the stratosphere, which is determined by stratospheric transport and chemistry, in particular by stratospheric residence time. Reflecting the different timescales and physico-chemical processes in the troposphere and stratosphere, the estimates are based on calculation of separate ensembles of trajectories for the troposphere and stratosphere. A methodology is described by which information from the two ensembles can be combined to give the ODPs.

    The ODP estimates for a species with a fixed 20 d lifetime, representing a compound like n-propyl bromide, are presented as an example. The estimated ODPs show strong geographical and seasonal variation, particularly within the tropics. The values of the ODPs are sensitive to the inclusion of a convective parametrization in the trajectory calculations, but the relative spatial and seasonal variation is not. The results imply that ODPs are largest for emissions from south and south-east Asia during Northern Hemisphere summer and from the western Pacific during Northern Hemisphere winter. Large ODPs are also estimated for emissions throughout the tropics with non-negligible values also extending into northern mid-latitudes, particularly in the summer. These first estimates, whilst made under some simplifying assumptions, show larger ODPs for certain emission regions, particularly south Asia in NH summer, than have typically been reported by previous studies which used emissions distributed evenly over land surfaces.

  2. Synchronous volcanic eruptions and abrupt climate change ˜17.7 ka plausibly linked by stratospheric ozone depletion

    Science.gov (United States)

    McConnell, Joseph R.; Burke, Andrea; Dunbar, Nelia W.; Köhler, Peter; Thomas, Jennie L.; Arienzo, Monica M.; Chellman, Nathan J.; Maselli, Olivia J.; Sigl, Michael; Adkins, Jess F.; Baggenstos, Daniel; Burkhart, John F.; Brook, Edward J.; Buizert, Christo; Cole-Dai, Jihong; Fudge, T. J.; Knorr, Gregor; Graf, Hans-F.; Grieman, Mackenzie M.; Iverson, Nels; McGwire, Kenneth C.; Mulvaney, Robert; Paris, Guillaume; Rhodes, Rachael H.; Saltzman, Eric S.; Severinghaus, Jeffrey P.; Steffensen, Jørgen Peder; Taylor, Kendrick C.; Winckler, Gisela

    2017-09-01

    Glacial-state greenhouse gas concentrations and Southern Hemisphere climate conditions persisted until ˜17.7 ka, when a nearly synchronous acceleration in deglaciation was recorded in paleoclimate proxies in large parts of the Southern Hemisphere, with many changes ascribed to a sudden poleward shift in the Southern Hemisphere westerlies and subsequent climate impacts. We used high-resolution chemical measurements in the West Antarctic Ice Sheet Divide, Byrd, and other ice cores to document a unique, ˜192-y series of halogen-rich volcanic eruptions exactly at the start of accelerated deglaciation, with tephra identifying the nearby Mount Takahe volcano as the source. Extensive fallout from these massive eruptions has been found >2,800 km from Mount Takahe. Sulfur isotope anomalies and marked decreases in ice core bromine consistent with increased surface UV radiation indicate that the eruptions led to stratospheric ozone depletion. Rather than a highly improbable coincidence, circulation and climate changes extending from the Antarctic Peninsula to the subtropics—similar to those associated with modern stratospheric ozone depletion over Antarctica—plausibly link the Mount Takahe eruptions to the onset of accelerated Southern Hemisphere deglaciation ˜17.7 ka.

  3. Stratospheric ozone depletion due to nitrous oxide: influences of other gases

    Science.gov (United States)

    Portmann, R. W.; Daniel, J. S.; Ravishankara, A. R.

    2012-01-01

    The effects of anthropogenic emissions of nitrous oxide (N2O), carbon dioxide (CO2), methane (CH4) and the halocarbons on stratospheric ozone (O3) over the twentieth and twenty-first centuries are isolated using a chemical model of the stratosphere. The future evolution of ozone will depend on each of these gases, with N2O and CO2 probably playing the dominant roles as halocarbons return towards pre-industrial levels. There are nonlinear interactions between these gases that preclude unambiguously separating their effect on ozone. For example, the CH4 increase during the twentieth century reduced the ozone losses owing to halocarbon increases, and the N2O chemical destruction of O3 is buffered by CO2 thermal effects in the middle stratosphere (by approx. 20% for the IPCC A1B/WMO A1 scenario over the time period 1900–2100). Nonetheless, N2O is expected to continue to be the largest anthropogenic emission of an O3-destroying compound in the foreseeable future. Reductions in anthropogenic N2O emissions provide a larger opportunity for reduction in future O3 depletion than any of the remaining uncontrolled halocarbon emissions. It is also shown that 1980 levels of O3 were affected by halocarbons, N2O, CO2 and CH4, and thus may not be a good choice of a benchmark of O3 recovery. PMID:22451111

  4. Vortex-averaged Arctic ozone depletion in the winter 2002/2003

    Directory of Open Access Journals (Sweden)

    T. Christensen

    2005-01-01

    Full Text Available A total ozone depletion of 68±7 Dobson units between 380 and 525K from 10 December 2002 to 10 March 2003 is derived from ozone sonde data by the vortex-average method, taking into account both diabatic descent of the air masses and transport of air into the vortex. When the vortex is divided into three equal-area regions, the results are 85±9DU for the collar region (closest to the edge, 52±5DU for the vortex centre and 68±7DU for the middle region in between centre and collar. Our results compare well with other studies: We find good agreement with ozone loss deduced from SAOZ data, with results inferred from POAM III observations and with results from tracer-tracer correlations using HF as the long-lived tracer. We find a higher ozone loss than that deduced by tracer-tracer correlations using CH4. We have made a careful comparison with Match results: The results were recalculated using a common time period, vortex edge definition and height interval. The two methods generally compare very well, except at the 475K level which exhibits an unexplained discrepancy.

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

    Science.gov (United States)

    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.

  6. A Model of the Effect of Ozone Depletion on Lower-Stratospheric Structure

    Science.gov (United States)

    Olsen, Mark A.; Stolarski, Richard S.; Gupta, Mohan L.; Nielsen, J. Eric; Pawson, Steven

    2005-01-01

    We have run two twenty-year integrations of a global circulation model using 1978-1980 and 1998-2000 monthly mean ozone climatologies. The ozone climatology is used solely in the radiation scheme of the model. Several key differences between the model runs will be presented. The temperature and potential vorticity (PV) structure of the lower stratosphere, particularly in the Southern Hemisphere, is significantly changed using the 1998-2000 ozone climatology. In the Southern Hemisphere summer, the lapse rate and PV-defined polar tropopauses are both at altitudes on the order of several hundred meters greater than the 1978-1980 climatological run. The 380 K potential temperature surf= is likewise at a greater altitude. The mass of the extratropical lowermost stratosphere (between the tropopause and 380 K surface) remains unchanged. The altitude differences are not observed in the Northern Hemisphere. The different ozone fields do not produce a significant change in the annual extratropical stratosphere-troposphere exchange of mass although slight variations in the spatial distribution of the exchange exist. We are also investigating a delay in the breakup of the Southern Hemisphere polar vortex due to the differing ozone climatologies.

  7. Lifetimes of Stratospheric Ozone-Depleting Substances, Their Replacements, and Related Species

    Science.gov (United States)

    Newman, P. A.; Ko, M. K.; Reimann, S.; Strahan, S. E.; Atlas, E. L.; Burkholder, J. B.; Chipperfield, M.; Engel, A.; Liang, Q.; Plumb, R. A.; Stolarski, R. S.

    2013-12-01

    Estimating the average lifetime of a chemical in the atmosphere is crucial to understanding its current and future atmospheric concentration. Furthermore, for both ozone depleting substances (ODSs) and greenhouse gases, information on their lifetimes is of paramount importance for obtaining future estimates for ozone depletion and climate forcing. The 'Lifetimes of Stratospheric Ozone-Depleting Substances, Their Replacements, and Related Species', under the World Climate Research Programme/Stratospheric Processes And their Role in Climate project, was completed in August 2013. The goal was to estimate both lifetimes and uncertainties. In this presentation we will provide: 1) an overview of key aspects of the definitions of lifetimes, 2) discuss the extensively revised photochemical values and uncertainties for obtaining lifetimes, 3) show new observational and 4) modeling estimates of lifetimes, and finally, 5) show new recommendations for the steady-state atmospheric lifetimes of 27 long-lived species. New findings include: * New chemical kinetic and photochemical information on the uncertainties associated with the Lyman-a absorption cross-sections, and revisions of absorption cross-section parameterizations for several chlorofluorocarbons. * State-of-the-art chemistry-climate models (CCMs) were used to estimate lifetimes over the course of the 21st century. Projected increases of the Brewer-Dobson circulation suggest that lifetimes should be shorter during the 21st century. However, the recovery of ozone in the CCMs shows that the photolysis of many species will decline, yielding only small changes in lifetimes of most species * The CFC-11 recommended lifetime increases to 52 years from the WMO (2011) value of 45 years. The most likely range is narrowed to 43-67 years. * The 44 year steady-state lifetime of CCl4 due to atmospheric loss determined in this report is substantially longer than the 35 years from WMO (2011). However, inclusion of the land and ocean

  8. Atmospheric lifetimes and Ozone Depletion Potentials of trans-1-chloro-3,3,3-trifluoropropylene and trans-1,2-dichloroethylene in a three-dimensional model

    Directory of Open Access Journals (Sweden)

    K. O. Patten

    2010-11-01

    Full Text Available The chloroalkenes trans-1-chloro-3,3,3-trifluoropropylene (tCFP and trans-1,2-dichloroethylene (tDCE have been proposed as candidate replacements for other compounds in current use that cause concerns regarding potential environmental effects including destruction of stratospheric ozone. Because tCFP and tDCE contain chlorine atoms, the effects of these short-lived compounds on stratospheric ozone must be established. In this study, we derive the atmospheric lifetimes and Ozone Depletion Potentials (ODPs for tCFP and for tDCE assuming emissions from land surfaces at latitudes 30° N to 60° N using the MOZART 3 three-dimensional model of atmospheric chemistry and physics. 53% of the ozone loss due to tCFP and 98% of the ozone loss due to tDCE take place in the troposphere, rather than in the stratosphere as generally expected from longer-lived chlorocarbons. The atmospheric lifetime of tCFP against chemical reaction is 40.4 days, and its ODP is quite small at 0.00034. The tDCE atmospheric lifetime is 12.7 days, and its ODP is 0.00024, which is the lowest ODP found for any chlorocarbon we have studied. Our study suggests that chlorine from tCFP and tDCE are unlikely to affect ozone at quantities likely to be emitted to the atmosphere.

  9. Depletion of the ozone layer: consequences for non-infectious human diseases

    International Nuclear Information System (INIS)

    Bentham, G.

    1993-01-01

    Stratospheric ozone depletion threatens to increase exposure to ultraviolet (UV) radiation which is known to be a factor in a number of diseases. There is little doubt that cumulative exposure to UV radiation is important in the aetiology of non-melanoma skin cancers. Evidence is also strong for a link with cutaneous malignant melanoma, although here it appears to be intermittent intense exposure that is most damaging. More controversial is the view that exposure to solar radiation is a significant factor in ocular damage, particularly in the formation of cataracts. Earlier studies pointing to such an effect have been criticized and alternative aetiological hypotheses have been proposed. However, other studies do show an effect of UV exposure on cortical cataract. Concern is also growing that UV may be capable of activating viruses and have immunological effects that might exacerbate infectious disease. Very worrying is the possibility that UV exposure can activate the human immunodeficiency virus which might accelerate the onset AIDS. Any such health effects that have been observed in human populations are the result of exposure to existing, naturally occurring levels of UV radiation. There is, therefore, great concern about the possible exacerbation of these impacts as a result of increased exposure to UV radiation associated with stratospheric ozone depletion. However, any assessment of the nature and scale of such impacts on human health has to deal with several major problems and these are the focus of this paper. There are uncertainties about recent trends in stratospheric ozone and problems in the prediction of future changes

  10. Fate of Chloromethanes in the Atmospheric Environment: Implications for Human Health, Ozone Formation and Depletion, and Global Warming Impacts

    Science.gov (United States)

    Tsai, Wen-Tien

    2017-01-01

    Among the halogenated hydrocarbons, chloromethanes (i.e., methyl chloride, CH3Cl; methylene chloride, CH2Cl2; chloroform, CHCl3; and carbon tetrachloride, CCl4) play a vital role due to their extensive uses as solvents and chemical intermediates. This article aims to review their main chemical/physical properties and commercial/industrial uses, as well as the environment and health hazards posed by them and their toxic decomposition products. The environmental properties (including atmospheric lifetime, radiative efficiency, ozone depletion potential, global warming potential, photochemical ozone creation potential, and surface mixing ratio) of these chlorinated methanes are also reviewed. In addition, this paper further discusses their atmospheric fates and human health implications because they are apt to reside in the lower atmosphere when released into the environment. According to the atmospheric degradation mechanism, their toxic degradation products in the troposphere include hydrogen chloride (HCl), carbon monoxide (CO), chlorine (Cl2), formyl chloride (HCOCl), carbonyl chloride (COCl2), and hydrogen peroxide (H2O2). Among them, COCl2 (also called phosgene) is a powerful irritating gas, which is easily hydrolyzed or thermally decomposed to form hydrogen chloride. PMID:29051455

  11. Fate of Chloromethanes in the Atmospheric Environment: Implications for Human Health, Ozone Formation and Depletion, and Global Warming Impacts.

    Science.gov (United States)

    Tsai, Wen-Tien

    2017-09-21

    Among the halogenated hydrocarbons, chloromethanes (i.e., methyl chloride, CH₃Cl; methylene chloride, CH₂Cl₂; chloroform, CHCl₃; and carbon tetrachloride, CCl₄) play a vital role due to their extensive uses as solvents and chemical intermediates. This article aims to review their main chemical/physical properties and commercial/industrial uses, as well as the environment and health hazards posed by them and their toxic decomposition products. The environmental properties (including atmospheric lifetime, radiative efficiency, ozone depletion potential, global warming potential, photochemical ozone creation potential, and surface mixing ratio) of these chlorinated methanes are also reviewed. In addition, this paper further discusses their atmospheric fates and human health implications because they are apt to reside in the lower atmosphere when released into the environment. According to the atmospheric degradation mechanism, their toxic degradation products in the troposphere include hydrogen chloride (HCl), carbon monoxide (CO), chlorine (Cl₂), formyl chloride (HCOCl), carbonyl chloride (COCl₂), and hydrogen peroxide (H₂O₂). Among them, COCl₂ (also called phosgene) is a powerful irritating gas, which is easily hydrolyzed or thermally decomposed to form hydrogen chloride.

  12. Effects of ozone-vegetation coupling on surface ozone air quality via biogeochemical and meteorological feedbacks

    Science.gov (United States)

    Sadiq, Mehliyar; Tai, Amos P. K.; Lombardozzi, Danica; Martin, Maria Val

    2017-02-01

    Tropospheric ozone is one of the most hazardous air pollutants as it harms both human health and plant productivity. Foliage uptake of ozone via dry deposition damages photosynthesis and causes stomatal closure. These foliage changes could lead to a cascade of biogeochemical and biogeophysical effects that not only modulate the carbon cycle, regional hydrometeorology and climate, but also cause feedbacks onto surface ozone concentration itself. In this study, we implement a semi-empirical parameterization of ozone damage on vegetation in the Community Earth System Model to enable online ozone-vegetation coupling, so that for the first time ecosystem structure and ozone concentration can coevolve in fully coupled land-atmosphere simulations. With ozone-vegetation coupling, present-day surface ozone is simulated to be higher by up to 4-6 ppbv over Europe, North America and China. Reduced dry deposition velocity following ozone damage contributes to ˜ 40-100 % of those increases, constituting a significant positive biogeochemical feedback on ozone air quality. Enhanced biogenic isoprene emission is found to contribute to most of the remaining increases, and is driven mainly by higher vegetation temperature that results from lower transpiration rate. This isoprene-driven pathway represents an indirect, positive meteorological feedback. The reduction in both dry deposition and transpiration is mostly associated with reduced stomatal conductance following ozone damage, whereas the modification of photosynthesis and further changes in ecosystem productivity are found to play a smaller role in contributing to the ozone-vegetation feedbacks. Our results highlight the need to consider two-way ozone-vegetation coupling in Earth system models to derive a more complete understanding and yield more reliable future predictions of ozone air quality.

  13. The role of bromine and chlorine chemistry for arctic ozone depletion events in Ny-Ålesund and comparison with model calculations

    Directory of Open Access Journals (Sweden)

    M. Martinez

    1999-07-01

    Full Text Available During the Arctic Tropospheric Ozone Chemistry (ARCTOC campaigns at Ny-Ålesund, Spitsbergen, the role of halogens in the depletion of boundary layer ozone was investigated. In spring 1995 and 1996 up to 30 ppt bromine monoxide were found whenever ozone decreased from normal levels of about 40 ppb. Those main trace gases and others were specifically followed in the UV-VIS spectral region by differential optical absorption spectroscopy (DOAS along light paths running between 20 and 475 m a.s.l.. The daily variation of peroxy radicals closely followed the ozone photolysis rate J(O3(O1D in the absence of ozone depletion most of the time. However, during low ozone events this close correlation was no longer found because the measurement of radicals by chemical amplification (CA turned out to be sensitive to peroxy radicals and ClOx. Large CA signals at night can sometimes definitely be assigned to ClOx and reached up to 2 ppt. Total bromine and iodine were both stripped quantitatively from air by active charcoal traps and measured after neutron activation of the samples. Total bromine increased from background levels of about 15 ppt to a maximum of 90 ppt during an event of complete ozone depletion. For the spring season a strong source of bromine is identified in the pack ice region according to back trajectories. Though biogenic emission sources cannot be completely ruled out, a primary activation of halogenides by various oxidants seems to initiate an efficient autocatalytic process, mainly driven by ozone and light, on ice and perhaps on aerosols. Halogenides residing on pack ice surfaces are continuously oxidised by hypohalogenous acids releasing bromine and chlorine into the air. During transport and especially above open water this air mixes with upper layer pristine air. As large quantities of bromine, often in the form of BrO, have been observed at polar sunrise also around Antarctica, its release seems to be a natural phenomenon. The

  14. The role of bromine and chlorine chemistry for arctic ozone depletion events in Ny-Ålesund and comparison with model calculations

    Directory of Open Access Journals (Sweden)

    M. Martinez

    Full Text Available During the Arctic Tropospheric Ozone Chemistry (ARCTOC campaigns at Ny-Ålesund, Spitsbergen, the role of halogens in the depletion of boundary layer ozone was investigated. In spring 1995 and 1996 up to 30 ppt bromine monoxide were found whenever ozone decreased from normal levels of about 40 ppb. Those main trace gases and others were specifically followed in the UV-VIS spectral region by differential optical absorption spectroscopy (DOAS along light paths running between 20 and 475 m a.s.l.. The daily variation of peroxy radicals closely followed the ozone photolysis rate J(O3(O1D in the absence of ozone depletion most of the time. However, during low ozone events this close correlation was no longer found because the measurement of radicals by chemical amplification (CA turned out to be sensitive to peroxy radicals and ClOx. Large CA signals at night can sometimes definitely be assigned to ClOx and reached up to 2 ppt. Total bromine and iodine were both stripped quantitatively from air by active charcoal traps and measured after neutron activation of the samples. Total bromine increased from background levels of about 15 ppt to a maximum of 90 ppt during an event of complete ozone depletion. For the spring season a strong source of bromine is identified in the pack ice region according to back trajectories. Though biogenic emission sources cannot be completely ruled out, a primary activation of halogenides by various oxidants seems to initiate an efficient autocatalytic process, mainly driven by ozone and light, on ice and perhaps on aerosols. Halogenides residing on pack ice surfaces are continuously oxidised by hypohalogenous acids releasing bromine and chlorine into the air. During transport and especially above open water this air mixes with upper layer pristine air. As large quantities of bromine, often in the form of BrO, have been observed at polar sunrise also around Antarctica, its release

  15. Carbonate precipitation in brine – a potential trigger for tropospheric ozone depletion events

    Directory of Open Access Journals (Sweden)

    R. Sander

    2006-01-01

    Full Text Available Tropospheric ozone depletion events (ODEs at high latitudes were discovered 20 years ago and are attributed to bromine explosions. However, an unresolved issue is the explanation of how the acid-catalyzed reaction cycle is triggered in atmospheric particles derived from alkaline sea water. By simulating the chemistry occuring in polar regions over recently formed sea ice, we can model successfully the transformation of inert sea-salt bromide to reactive bromine monoxide (BrO and the subsequent ODE when precipitation of calcium carbonate from freezing sea water is taken into account. In addition, we found the temperature dependence of the equilibrium BrCl+Br−↔Br2Cl− to be important.

  16. Mineral dust variability in central West Antarctica associated with ozone depletion

    Directory of Open Access Journals (Sweden)

    M. Cataldo

    2013-02-01

    Full Text Available We present here data of mineral dust variability retrieved from an ice core of the central West Antarctic, spanning the last five decades. Main evidence provided by the geochemical analysis is that northerly air mass incursions to the coring site, tracked by insoluble dust microparticles, have declined over the past 50 yr. This result contrasts with dust records from ice cores reported to the coastal West Antarctic that show increases since mid-20th century. We attribute this difference to regional climatic changes due to the ozone depletion and its implications to westerly winds. We found that the diameters of insoluble microparticles in the central West Antarctica ice core are significantly correlated with cyclone depth (energy and wind intensity around Antarctica.

  17. Future stratospheric ozone depletion will affect a subarctic dwarf shrub ecosystem

    Energy Technology Data Exchange (ETDEWEB)

    Johanson, Ulf

    1997-02-01

    The stratospheric ozone depletion and the concomitant increase in ultraviolet-B (UV-B, 280-320 nm) radiation is of global concern due to the effects of UV-B on living organisms. To investigate the effects of increased levels of UV-B, a field irradiation system was established at a subarctic dwarf shrub heath in Northern Sweden (68 deg N). An ozone depletion of 15% under clear sky conditions was simulated over a naturally growing ecosystem. The response of both individual components and processes was studied to reveal changes in ecosystem structure and function. Species with different life strategies (evergreen or deciduous) responded differently both in magnitude and direction. The evergreen species were more responsive to UV-B regarding shoot growth, which could be due to cumulative effects in long-lived tissues, since the retardation in relative growth increased over time of exposure. Leaves of evergreen species became thicker under enhanced UV-B, while leaves of deciduous species became thinner. Decomposition studies (laboratory and in situ) showed that indirect effects of UV-B, due to changes in leaf tissue chemistry affected microbial activity and slowed down the decomposition rate. More directly, UV-B decreased the abundance of some fungal species and hence the composition of species. However, no altered decomposition rate was found when decomposition progressed under high UV-B even if the microorganisms were fewer. This could be due to the increased direct photo degradation of litter that compensates for lower microbial activity. The decomposition rate is therefore strongly dependent on the interception of UV-B at the litter layer. This research has shown that ecosystem components and processes are affected in a number of ways and that there are indications of changes in species composition in a long-term perspective due to differences in responsiveness between the different species. 128 refs, 7 figs

  18. From aggregative adsorption to surface depletion

    DEFF Research Database (Denmark)

    Rother, Gernot; Müter, Dirk; Bock, Henry

    2017-01-01

    Adsorption of a short-chain nonionic amphiphile (C6E3) at the surface of mesoporous silica glass (CPG) was studied by a combination of adsorption measurements and mesoscale simulations. Adsorption measurements covering a wide composition range of the C6E3 + water system show that no adsorption...... occurs up to the critical micelle concentration, at which a sharp increase of adsorption is observed that is attributed to ad-micelle formation at the pore walls. Intriguingly, as the concentration is increased further, the surface excess of the amphiphile begins to decrease and eventually becomes...... negative, which corresponds to preferential adsorption of water rather than amphiphile at high amphiphile concentrations. The existence of such a surface-azeotropic point has not previously been reported in the surfactant adsorption field. Dissipative particle dynamics simulations were performed to reveal...

  19. Variability of surface ozone with cloud coverage over Kolkata, India

    Indian Academy of Sciences (India)

    Critical analysis of experimental surface ozone data and cloud coverage is reported over Kolkata during the period January 2011 to December 2011. Significant relationship between these two parameters is observed. Analysis shows that the trend of surface ozone concentration and cloud coverage follow opposite ...

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

    Science.gov (United States)

    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…

  1. Ozone-depleting substances and the greenhouse gases HFCs, PFCs and SF{sub 6}. Danish consumption and emissions, 2006

    Energy Technology Data Exchange (ETDEWEB)

    Sander Poulsen, T. (PlanMiljoe (Denmark))

    2007-07-01

    The objective of this project was to map the 2006 consumption of newly produced industrial ozone-depleting substances and the consumption and actual emissions of HFCs, PFCs, and SF{sub 6}. The evaluation was made in accordance with the IPCC guidelines and following the method employed in previous evaluations. (BA)

  2. Ozone kinetics in low-pressure discharges: vibrationally excited ozone and molecule formation on surfaces

    International Nuclear Information System (INIS)

    Marinov, Daniil; Guaitella, Olivier; Booth, Jean-Paul; Rousseau, Antoine; Guerra, Vasco

    2013-01-01

    A combined experimental and modeling investigation of the ozone kinetics in the afterglow of pulsed direct current discharges in oxygen is carried out. The discharge is generated in a cylindrical silica tube of radius 1 cm, with short pulse durations between 0.5 and 2 ms, pressures in the range 1–5 Torr and discharge currents ∼40–120 mA. Time-resolved absolute concentrations of ground-state atoms and ozone molecules were measured simultaneously in situ, by two-photon absorption laser-induced fluorescence and ultraviolet absorption, respectively. The experiments were complemented by a self-consistent model developed to interpret the results and, in particular, to evaluate the roles of vibrationally excited ozone and of ozone formation on surfaces. It is found that vibrationally excited ozone, O 3 * , plays an important role in the ozone kinetics, leading to a decrease in the ozone concentration and an increase in its formation time. In turn, the kinetics of O 3 * is strongly coupled with those of atomic oxygen and O 2 (a 1 Δ g ) metastables. Ozone formation at the wall does not contribute significantly to the total ozone production under the present conditions. Upper limits for the effective heterogeneous recombination probability of O atoms into ozone are established. (paper)

  3. Ozone kinetics in low-pressure discharges: vibrationally excited ozone and molecule formation on surfaces

    Science.gov (United States)

    Marinov, Daniil; Guerra, Vasco; Guaitella, Olivier; Booth, Jean-Paul; Rousseau, Antoine

    2013-10-01

    A combined experimental and modeling investigation of the ozone kinetics in the afterglow of pulsed direct current discharges in oxygen is carried out. The discharge is generated in a cylindrical silica tube of radius 1 cm, with short pulse durations between 0.5 and 2 ms, pressures in the range 1-5 Torr and discharge currents ˜40-120 mA. Time-resolved absolute concentrations of ground-state atoms and ozone molecules were measured simultaneously in situ, by two-photon absorption laser-induced fluorescence and ultraviolet absorption, respectively. The experiments were complemented by a self-consistent model developed to interpret the results and, in particular, to evaluate the roles of vibrationally excited ozone and of ozone formation on surfaces. It is found that vibrationally excited ozone, O_3^{*} , plays an important role in the ozone kinetics, leading to a decrease in the ozone concentration and an increase in its formation time. In turn, the kinetics of O_3^{*} is strongly coupled with those of atomic oxygen and O2(a 1Δg) metastables. Ozone formation at the wall does not contribute significantly to the total ozone production under the present conditions. Upper limits for the effective heterogeneous recombination probability of O atoms into ozone are established.

  4. Ozone-depleting substances and the greenhouse gases HFCs, PFCs and SF6. Danish consumption and emissions, 2004

    Energy Technology Data Exchange (ETDEWEB)

    Sander Poulsen, T. [PlanMiljoe (Denmark)

    2006-05-19

    The objective of this project was to map the 2004 consumption of newly produced industrial ozone-depleting substances and the consumption and actual emissions of HFCs, PFCs, and SF6. The evaluation was made in accordance with the IPCC guidelines, and following the method employed in previous evaluations and it covers the net consumption of ozone-depleting substances. The term 'net consumption' is understood as the amount of imported goods in bulk or drums, less any re-export of substances as raw materials. Ozone-depleting substances contained in finished products that are imported and exported are not included in the evaluation. This delimitation is in full compliance with international guidelines. The evaluation does not account for the consumption of ozone-depleting substances used as raw material in the production of other substances, such as tetra chloromethane, and which are not subsequently emitted to the atmosphere. The information on consumption has been gathered from importers, suppliers and enterprise end-users (usually purchasing departments), and Statistics Denmark. This method of data gathering means that the information gathered is about the quantities of substances traded. Purchase and sales figures are used as an expression of consumption. This approach is considered to be suitable and adequate for the present purpose, since experience from previous projects shows that a levelling out occurs with time and that the substances sold/purchased are consumed within a relatively small time horizon. None of the substances covered here are produced in Denmark. Furthermore, ozone-depleting substances are treated at chemical waste processing plants in Denmark. Treatment and destruction data was gathered for the evaluation, but in line with all previous evaluations it has not been accounted for in the consumption figures. (BA)

  5. Surface ozone in the urban area of Manaus, Amazonas, Brazil

    Science.gov (United States)

    Souza, R. A. F. D.; Costa, P. S.; Silva, C.; Godoi, R. M.; Martin, S. T.; Tota, J.; Barbosa, H. M.; Pauliquevis, T.; Ferreira De Brito, J.; Artaxo, P.; Manzi, A. O.; Wolf, S. A.; Cirino, G. G.

    2014-12-01

    When nitrogen oxides from vehicle and industrial emissions mix with volatile organic compounds from trees and plants with exposure to sunlight, a chemical reaction occurs contributing to ground-level ozone pollution. The preliminary results of the surface ozone study in urban area of Manaus, Amazonas State, Brazil, are presented for the first intensive operating period (IOP1) of the GoAmazon experiment (February/March 2014). Photochemical ozone production was found to be a regular process, with an afternoon maximum of the ozone mixing ratio of lower than 20 ppbv for cloudy days or clear sky weather. Typical ozone concentrations at mid-day were low (about 10 ppb). On the other hand, several high-value ozone episodes with surface ozone mixing ratios up to three times larger were registered during the dry season of 2013 (September/October). At the beginning of the wet season, the ozone concentration in Manaus decreased significantly, but diurnal variations can be found during the days with rainfall and other fast changes of meteorological conditions. Possible explanations of the nature of pulsations are discussed. Photochemical ozone production by local urban plumes of Manaus is named as a first possible source of the ozone concentration and biomass burning or power plant emissions are suggested as an alternative or an additional source.

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

    Directory of Open Access Journals (Sweden)

    S. Falk

    2018-03-01

    Full Text Available 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.

  7. Responses of Surface Ozone Air Quality to Anthropogenic Nitrogen Deposition

    Science.gov (United States)

    Zhang, L.; Zhao, Y.; Tai, A. P. K.; Chen, Y.; Pan, Y.

    2017-12-01

    Human activities have substantially increased atmospheric deposition of reactive nitrogen to the Earth's surface, inducing unintentional effects on ecosystems with complex environmental and climate consequences. One consequence remaining unexplored is how surface air quality might respond to the enhanced nitrogen deposition through surface-atmosphere exchange. We combine a chemical transport model (GEOS-Chem) and a global land model (Community Land Model) to address this issue with a focus on ozone pollution in the Northern Hemisphere. We consider three processes that are important for surface ozone and can be perturbed by addition of atmospheric deposited nitrogen: emissions of biogenic volatile organic compounds (VOCs), ozone dry deposition, and soil nitrogen oxide (NOx) emissions. We find that present-day anthropogenic nitrogen deposition (65 Tg N a-1 to the land), through enhancing plant growth (represented as increases in vegetation leaf area index (LAI) in the model), could increase surface ozone from increased biogenic VOC emissions, but could also decrease ozone due to higher ozone dry deposition velocities. Meanwhile, deposited anthropogenic nitrogen to soil enhances soil NOx emissions. The overall effect on summer mean surface ozone concentrations show general increases over the globe (up to 1.5-2.3 ppbv over the western US and South Asia), except for some regions with high anthropogenic NOx emissions (0.5-1.0 ppbv decreases over the eastern US, Western Europe, and North China). We compare the surface ozone changes with those driven by the past 20-year climate and historical land use changes. We find that the impacts from anthropogenic nitrogen deposition can be comparable to the climate and land use driven surface ozone changes at regional scales, and partly offset the surface ozone reductions due to land use changes reported in previous studies. Our study emphasizes the complexity of biosphere-atmosphere interactions, which can have important

  8. A study of polar ozone depletion based on sequential assimilation of satellite data from the ENVISAT/MIPAS and Odin/SMR instruments

    Directory of Open Access Journals (Sweden)

    J. D. Rösevall

    2007-01-01

    Full Text Available The objective of this study is to demonstrate how polar ozone depletion can be mapped and quantified by assimilating ozone data from satellites into the wind driven transport model DIAMOND, (Dynamical Isentropic Assimilation Model for OdiN Data. By assimilating a large set of satellite data into a transport model, ozone fields can be built up that are less noisy than the individual satellite ozone profiles. The transported fields can subsequently be compared to later sets of incoming satellite data so that the rates and geographical distribution of ozone depletion can be determined. By tracing the amounts of solar irradiation received by different air parcels in a transport model it is furthermore possible to study the photolytic reactions that destroy ozone. In this study, destruction of ozone that took place in the Antarctic winter of 2003 and in the Arctic winter of 2002/2003 have been examined by assimilating ozone data from the ENVISAT/MIPAS and Odin/SMR satellite-instruments. Large scale depletion of ozone was observed in the Antarctic polar vortex of 2003 when sunlight returned after the polar night. By mid October ENVISAT/MIPAS data indicate vortex ozone depletion in the ranges 80–100% and 70–90% on the 425 and 475 K potential temperature levels respectively while the Odin/SMR data indicates depletion in the ranges 70–90% and 50–70%. The discrepancy between the two instruments has been attributed to systematic errors in the Odin/SMR data. Assimilated fields of ENVISAT/MIPAS data indicate ozone depletion in the range 10–20% on the 475 K potential temperature level, (~19 km altitude, in the central regions of the 2002/2003 Arctic polar vortex. Assimilated fields of Odin/SMR data on the other hand indicate ozone depletion in the range 20–30%.

  9. Fabrication and characterization of fully depleted surface barrier detectors

    International Nuclear Information System (INIS)

    Ray, A.

    2010-01-01

    Fabrication of fully depleted surface barrier type thin detectors needs thin silicon wafer of 20 - 30 μm thickness and flatness of ± 1 μm. Process has been developed for thinning silicon wafers to achieve thickness up to 20 - 30 μm from thicker (0.5 - 0.8 mm) silicon samples. These samples were used to fabricate fully depleted surface barrier detectors using Au contacts on n-type silicon. The detectors were characterized by measuring forward and reverse I-V characteristics and alpha energy spectra of Am-Pu source. (author)

  10. Nicotiana tabacum as model for ozone - plant surface reactions

    Science.gov (United States)

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

    2015-04-01

    Elevated tropospheric ozone concentrations are considered a toxic threat to plants, responsible for global crop losses with associated economic costs of several billion dollars per year. The ensuing injuries have been related to the uptake of ozone through the stomatal pores and oxidative effects damaging the internal leaf tissue. A striking question of current research is the environment and plant specific partitioning of ozone loss between gas phase, stomatal or plant surface sink terms. Here we show results from ozone fumigation experiments using various Nicotiana Tabacum varieties, whose surfaces are covered with different amounts of unsaturated diterpenoids exuded by their glandular trichomes. Exposure to elevated ozone levels (50 to 150 ppbv) for 5 to 15 hours in an exceptionally clean cuvette system did neither result in a reduction of photosynthesis nor caused any visible leaf damage. Both these ozone induced stress effects have been observed previously in ozone fumigation experiments with the ozone sensitive tobacco line Bel-W3. In our case ozone fumigation was accompanied by a continuous release of oxygenated volatile organic compounds, which could be clearly associated to their condensed phase precursors for the first time. Gas phase reactions of ozone were avoided by choosing a high enough gas exchange rate of the plant cuvette system. In the case of the Ambalema variety, that is known to exude only the diterpenoid cis-abienol, ozone fumigation experiments yield the volatiles formaldehyde and methyl vinyl ketone (MVK). The latter could be unequivocally separated from isomeric methacrolein (MACR) by the aid of a Selective Reagent Ion Time-of-Flight Mass Spectrometer (SRI-ToF-MS), which was switched every six minutes from H3O+ to NO+ primary ion mode and vice versa. Consistent with the picture of an ozone protection mechanism caused by reactive diterpenoids at the leaf surface are the results from dark-light experiments. The ozone loss obtained from the

  11. Surface ozone characterization at Larsemann Hills and Maitri, Antarctica.

    Science.gov (United States)

    Ali, Kaushar; Trivedi, D K; Sahu, S K

    2017-04-15

    Data are analyzed in terms of daily average ozone, its diurnal variation and its relation with meteorological parameters like dry bulb temperature (T), wet bulb temperature (T w ), atmospheric pressure and wind speed based on measurement of these parameters at two Indian Antarctic stations (Larsemann Hills, and Maitri) during 28th Indian Scientific Expedition of Antarctica (ISEA) organized during Antarctic summer of the year 2008-09. The work has been carried out to investigate summer time ozone level and its day-to-day and diurnal variability at these coastal locations and to highlight possible mechanism of ozone production and destruction. The result of the analysis indicates that daily average ozone concentration at Larsemann Hills varied from ~13 and ~20ppb with overall average value of ~16ppb and at Maitri, it varied from ~16 and ~21ppb with overall average value of ~18ppb. Photochemistry is found to partially contribute occasionally to the surface layer ozone at both the stations. Lower concentration of ozone at Maitri during beginning of the observational days may be due to destruction of ozone through activated halogens, whereas higher ozone on latter days may be due to photochemistry and advective transport from east to south-east areas. Ozone concentration during blizzard episodes at both the stations is reduced due to slow photochemical production of ozone, its photochemical removal and removal through deposition of ozone molecules on precipitation particles. Diurnal variation of ozone at Larsemann Hills and Maitri has been found to be absent. Copyright © 2017 Elsevier B.V. All rights reserved.

  12. The TOAR database on observations of surface ozone (and more)

    Science.gov (United States)

    Schultz, M. G.; Schröder, S.; Cooper, O. R.; Galbally, I. E.; Petropavlovskikh, I. V.; von Schneidemesser, E.; Tanimoto, H.; Elshorbany, Y. F.; Naja, M. K.; Seguel, R. J.

    2017-12-01

    In support of the first Tropospheric Ozone Assessment Report (TOAR) a relational database of global surface ozone observations has been developed and populated with hourly measurement data and enhanced metadata. A comprehensive suite of ozone data products including standard statistics, health and vegetation impact metrics, and trend information, are made available through a common data portal and a web interface. These data form the basis of the TOAR analyses focusing on human health, vegetation, and climate relevant ozone issues. Cooperation among many data centers and individual researchers worldwide made it possible to build the world's largest collection of in-situ hourly surface ozone data covering the period from 1970 to 2015. By combining the data from almost 10,000 measurement sites around the world with global metadata information, new analyses of surface ozone have become possible, such as the first globally consistent characterisations of measurement sites as either urban or rural/remote. Exploitation of these global metadata allows for new insights into the global distribution, and seasonal and long-term changes of tropospheric ozone and they enable TOAR to perform the first, globally consistent analysis of present-day ozone concentrations and recent ozone changes with relevance to health, agriculture, and climate. This presentation will provide a summary of the TOAR surface observations database including recent additions of ozone precursor and meteorological data. We will demonstrate how the database can be accessed and the data can be used, and we will discuss its limitations and the potential for closing some of teh remaining data gaps.

  13. From ozone depletion to agriculture: understanding the role of UV radiation in sustainable crop production.

    Science.gov (United States)

    Wargent, Jason J; Jordan, Brian R

    2013-03-01

    Largely because of concerns regarding global climate change, there is a burgeoning interest in the application of fundamental scientific knowledge in order to better exploit environmental cues in the achievement of desirable endpoints in crop production. Ultraviolet (UV) radiation is an energetic driver of a diverse range of plant responses and, despite historical concerns regarding the damaging consequences of UV-B radiation for global plant productivity as related to stratospheric ozone depletion, current developments representative of a range of organizational scales suggest that key plant responses to UV-B radiation may be exploitable in the context of a sustainable contribution towards the strengthening of global crop production, including alterations in secondary metabolism, enhanced photoprotection, up-regulation of the antioxidative response and modified resistance to pest and disease attack. Here, we discuss the prospect of this paradigm shift in photobiology, and consider the linkages between fundamental plant biology and crop-level outcomes that can be applied to the plant UV-B response, in addition to the consequences for related biota and many other facets of agro-ecosystem processes. © 2013 The Author. New Phytologist © 2012 New Phytologist Trust.

  14. Ozone-depleting substances and the greenhouse gases HFCs, PFCs and SF{sub 6}. Danish consumption and emissions, 2005

    Energy Technology Data Exchange (ETDEWEB)

    Sander Poulsen, T. [PlanMiljoe (Denmark)

    2007-06-15

    An evaluation of Danish consumption and emissions of ozone-depleting substances and industrial greenhouse gases has been carried out in continuation of previous evaluations, partly to fulfil Denmark's international obligations to provide information within this area and partly to follow the trend in consumption of ozone-depleting substances as well as the consumption and emissions of HFCs, PFCs and SF{sub 6}. The evaluation includes a calculation of actual emissions of HFCs, PFCs, and SF{sub 6} for 2006. In this calculation the release from stock of greenhouse gases in products has been taken into account, and adjustments have been made for imports and exports of the greenhouse gases in products. (BA)

  15. Detectability of the impacts of ozone-depleting substances and greenhouse gases upon stratospheric ozone accounting for nonlinearities in historical forcings

    Science.gov (United States)

    Bandoro, Justin; Solomon, Susan; Santer, Benjamin D.; Kinnison, Douglas E.; Mills, Michael J.

    2018-01-01

    We perform a formal attribution study of upper- and lower-stratospheric ozone changes using observations together with simulations from the Whole Atmosphere Community Climate Model. Historical model simulations were used to estimate the zonal-mean response patterns (fingerprints) to combined forcing by ozone-depleting substances (ODSs) and well-mixed greenhouse gases (GHGs), as well as to the individual forcing by each factor. Trends in the similarity between the searched-for fingerprints and homogenized observations of stratospheric ozone were compared to trends in pattern similarity between the fingerprints and the internally and naturally generated variability inferred from long control runs. This yields estimated signal-to-noise (S/N) ratios for each of the three fingerprints (ODS, GHG, and ODS + GHG). In both the upper stratosphere (defined in this paper as 1 to 10 hPa) and lower stratosphere (40 to 100 hPa), the spatial fingerprints of the ODS + GHG and ODS-only patterns were consistently detectable not only during the era of maximum ozone depletion but also throughout the observational record (1984-2016). We also develop a fingerprint attribution method to account for forcings whose time evolutions are markedly nonlinear over the observational record. When the nonlinearity of the time evolution of the ODS and ODS + GHG signals is accounted for, we find that the S/N ratios obtained with the stratospheric ODS and ODS + GHG fingerprints are enhanced relative to standard linear trend analysis. Use of the nonlinear signal detection method also reduces the detection time - the estimate of the date at which ODS and GHG impacts on ozone can be formally identified. Furthermore, by explicitly considering nonlinear signal evolution, the complete observational record can be used in the S/N analysis, without applying piecewise linear regression and introducing arbitrary break points. The GHG-driven fingerprint of ozone changes was not statistically identifiable in either

  16. The dynamics of ozone generation and mode transition in air surface micro-discharge plasma at atmospheric pressure

    International Nuclear Information System (INIS)

    Shimizu, Tetsuji; Zimmermann, Julia L; Morfill, Gregor E; Sakiyama, Yukinori; Graves, David B

    2012-01-01

    We present the transient, dynamic behavior of ozone production in surface micro-discharge (SMD) plasma in ambient air. Ultraviolet absorption spectroscopy at 254 nm was used to measure the time development of ozone density in a confined volume. We observed that ozone density increases monotonically over 1000 ppm for at least a few minutes when the input power is lower than ∼0.1 W/cm 2 . Interestingly, when input power is higher than ∼0.1 W/cm 2 , ozone density starts to decrease in a few tens of seconds at a constant power density, showing a peak ozone density. A model calculation suggests that the ozone depletion at higher power density is caused by quenching reactions with nitrogen oxides that are in turn created by vibrationally excited nitrogen molecules reacting with O atoms. The observed mode transition is significantly different from classical ozone reactors in that the transition takes place over time at a constant power. In addition, we observed a positive correlation between time-averaged ozone density and the inactivation rate of Escherichia coli on adjacent agar plates, suggesting that ozone plays a key role in inactivating bacteria under the conditions considered here. (paper)

  17. Coincident Observations of Surface Ozone and NMVOCs over Abu Dhabi

    Science.gov (United States)

    Abbasi, Naveed; Majeed, Tariq; Iqbal, Mazhar; Tarasick, David; Davies, Jonathan; Riemer, Daniel; Apel, Eric

    2016-07-01

    The vertical profiles of ozone are measured coincidently with non-methane volatile organic compounds (NMVOCs) at the meteorological site located at the Abu Dhabi international airport (latitude 24.45N; longitude 54.22E) during the years 2012 - 2014. Some of the profiles show elevated surface ozone >95 ppbv during the winter months (December, January and February). The ground-level NMVOCs obtained from the gas chromatography-flame ionization detection/mass spectrometry system also show elevated values of acetylene, ethane, propane, butane, pentane, benzene, and toluene. NMVOCs and ozone abundances in other seasons are much lower than the values in winter season. NMVOCs are emitted from an extensive number of sources in urban environments including fuel production, distribution, and consumption, and serve as precursor of ozone. Transport sources contribute a substantial portion of the NMVOC burden to the urban atmosphere in developed regions. Abu Dhabi is located at the edge of the Arabian Gulf and is highly affected by emissions from petrochemical industries in the neighboring Gulf region. The preliminary results indicate that wintertime enhancement in ozone is associated with large values of NMVOCs at Abu Dhabi. The domestic production of surface ozone is estimated from the combination of oxygen recombination and NMVOCs and compared with the data. It is estimated that about 40-50% of ozone in Abu Dhabi is transported from the neighbouring petrochemical industries. We will present ozone sounding and NMVOCs data and our model estimates of surface ozone, including a discussion on the high levels of the tropospheric ozone responsible for contaminating the air quality in the UAE. This work is supported by National Research Foundation, UAE.

  18. Surface Ozone Dynamics in the Kola Peninsula Region

    Science.gov (United States)

    Beloglazov, M. I.; Karpechko, A. Yu.; Nikulin, G. N.; Roumjantsev, S. A.

    Measurements of surface ozone from the centre of the Murmansk Region (Apatity, Kola peninsula) and its southern part (Kovda, White Sea coast) give a picture of the behaviour of this air component on the Kola peninsula and surrounding vicinity. Simultaneous measurements in Apatity and Kovda have shown that the ozone concentration in Apatity is roughly twice as much as in Kovda. This fact may be explained by the local wind circulation and the presence of bromine near the coast of the Kola Peninsula. An inverse correlation is found between the ozone and nitrogen oxide concentrations from observations near motorways in Apatity. A decrease of nitrogen oxide concentration accompanies the growth of ozone on average. Thus, Apatity is a northern city in which the air pollution by traffic emissions decreases the ozone content.

  19. Damages of surface ozone: evidence from agricultural sector in China

    Science.gov (United States)

    Yi, Fujin; McCarl, Bruce A.; Zhou, Xun; Jiang, Fei

    2018-03-01

    This study measures the damages that surface ozone pollution causes within the Chinese agricultural sector under 2014 conditions. It also analyzes the agricultural benefits of ozone reductions. The analysis is done using a partial equilibrium model of China’s agricultural sector. Results indicate that there are substantial, spatially differentiated damages that are greatest in ozone-sensitive crop growing areas with higher ozone concentrations. The estimated damage to China’s agricultural sector range is between CNY 1.6 trillion and 2.2 trillion, which for comparison is about one fifth of 2014 agricultural revenue. When considering concentration reduction we find a 30% ozone reduction yields CNY 678 billion in sectoral benefits. These benefits largely fall to consumers with producers losing as the production gains lead to lower prices.

  20. Ozone Decomposition on the Surface of Metal Oxide Catalyst

    Directory of Open Access Journals (Sweden)

    Batakliev Todor Todorov

    2014-12-01

    Full Text Available The catalytic decomposition of ozone to molecular oxygen over catalytic mixture containing manganese, copper and nickel oxides was investigated in the present work. The catalytic activity was evaluated on the basis of the decomposition coefficient which is proportional to ozone decomposition rate, and it has been already used in other studies for catalytic activity estimation. The reaction was studied in the presence of thermally modified catalytic samples operating at different temperatures and ozone flow rates. The catalyst changes were followed by kinetic methods, surface measurements, temperature programmed reduction and IR-spectroscopy. The phase composition of the metal oxide catalyst was determined by X-ray diffraction. The catalyst mixture has shown high activity in ozone decomposition at wet and dry O3/O2 gas mixtures. The mechanism of catalytic ozone degradation was suggested.

  1. Transboundary Contributions To Surface Ozone In California's Central Valley

    Science.gov (United States)

    Post, A.; Faloona, I. C.; Conley, S. A.; Lighthall, D.

    2014-12-01

    Rising concern over the impacts of exogenous air pollution in California's Central Valley has prompted the establishment of a coastal, high altitude monitoring site at the Chews Ridge Observatory (1550 m) approximately 30 km east of Point Sur in Monterey County, under the auspices of the Monterey Institute for Research in Astronomy. Two and a half years of continuous ozone data are presented in the context of long-range transport and its potential impact on surface air quality in the San Joaquin Valley (SJV). Past attempts to quantify the impact of transboundary ozone on surface levels have relied on uncertain model estimates, or have been limited to weekly ozonesonde data. Here, we present an observationally derived quantification of the contribution of free tropospheric ozone to surface sites in the San Joaquin Valley throughout three ozone seasons (June through September, 2012-2014). The diurnal ozone patterns at Chews Ridge, and their correlations with ozone aloft over the Valley, have been presented previously. Furthermore, reanalysis data of geopotential heights indicate consistent flow from Chews Ridge to the East, directly over the SJV. In a related airborne project we quantify the vertical exchange, or entrainment, rate over the Southern SJV from a series of focused flights measuring ozone concentrations during peak photochemical hours in conjunction with local meteorological data to quantify an ozone budget for the area. By applying the entrainment rates observed in that study here we are able to quantify the seasonal contributions of free tropospheric ozone measured at Chews Ridge to surface sites in the San Joaquin Valley, and compare prior model estimates to our observationally derived values.

  2. Growth of soybean at future tropospheric ozone concentrations decreases canopy evapotranspiration and soil water depletion

    International Nuclear Information System (INIS)

    Bernacchi, Carl J.; Leakey, Andrew D.B.; Kimball, Bruce A.; Ort, Donald R.

    2011-01-01

    Tropospheric ozone is increasing in many agricultural regions resulting in decreased stomatal conductance and overall biomass of sensitive crop species. These physiological effects of ozone forecast changes in evapotranspiration and thus in the terrestrial hydrological cycle, particularly in intercontinental interiors. Soybean plots were fumigated with ozone to achieve concentrations above ambient levels over five growing seasons in open-air field conditions. Mean season increases in ozone concentrations ([O 3 ]) varied between growing seasons from 22 to 37% above background concentrations. The objective of this experiment was to examine the effects of future [O 3 ] on crop ecosystem energy fluxes and water use. Elevated [O 3 ] caused decreases in canopy evapotranspiration resulting in decreased water use by as much as 15% in high ozone years and decreased soil water removal. In addition, ozone treatment resulted in increased sensible heat flux in all years indicative of day-time increase in canopy temperature of up to 0.7 deg. C. - Highlights: → Globally, tropospheric ozone is currently and will likely continue to increase into the future. → We examine the impact of elevated ozone on water use by soybean at the SoyFACE research facility. → High ozone grown soybean had reduced rates of evapotranspiration and higher soil moisture. → Increases in ozone have the potential to impact the hydrologic cycle where these crops are grown. - Soybean grown in elevated concentrations of ozone is shown to evapotranspire less water compared with soybean canopies grown under current atmospheric conditions.

  3. Surface ozone scenario at Pune and Delhi during the decade of 1990s

    Indian Academy of Sciences (India)

    there is no trend whatsoever in the variation of surface ozone concentration at Delhi. Minimum value of surface ozone occurs before sunrise and maximum in the afternoon hours. Regression ... Introduction. Surface ozone is of immense societal concern due to .... in the presence of high concentration of ozone precursor ...

  4. 40 CFR Appendix H to Subpart A of... - Clean Air Act Amendments of 1990 Phaseout Schedule for Production of Ozone-Depleting Substances

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Clean Air Act Amendments of 1990 Phaseout Schedule for Production of Ozone-Depleting Substances H Appendix H to Subpart A of Part 82... STRATOSPHERIC OZONE Production and Consumption Controls Pt. 82, Subpt. A, App. H Appendix H to Subpart A of Part...

  5. Tropospheric Ozone Assessment Report: Database and Metrics Data of Global Surface Ozone Observations

    Directory of Open Access Journals (Sweden)

    Martin G. Schultz

    2017-10-01

    Full Text Available In support of the first Tropospheric Ozone Assessment Report (TOAR a relational database of global surface ozone observations has been developed and populated with hourly measurement data and enhanced metadata. A comprehensive suite of ozone data products including standard statistics, health and vegetation impact metrics, and trend information, are made available through a common data portal and a web interface. These data form the basis of the TOAR analyses focusing on human health, vegetation, and climate relevant ozone issues, which are part of this special feature. Cooperation among many data centers and individual researchers worldwide made it possible to build the world's largest collection of 'in-situ' hourly surface ozone data covering the period from 1970 to 2015. By combining the data from almost 10,000 measurement sites around the world with global metadata information, new analyses of surface ozone have become possible, such as the first globally consistent characterisations of measurement sites as either urban or rural/remote. Exploitation of these global metadata allows for new insights into the global distribution, and seasonal and long-term changes of tropospheric ozone and they enable TOAR to perform the first, globally consistent analysis of present-day ozone concentrations and recent ozone changes with relevance to health, agriculture, and climate. Considerable effort was made to harmonize and synthesize data formats and metadata information from various networks and individual data submissions. Extensive quality control was applied to identify questionable and erroneous data, including changes in apparent instrument offsets or calibrations. Such data were excluded from TOAR data products. Limitations of 'a posteriori' data quality assurance are discussed. As a result of the work presented here, global coverage of surface ozone data for scientific analysis has been significantly extended. Yet, large gaps remain in the surface

  6. Ultraviolet-Ozone Cleaning of Semiconductor Surfaces

    Science.gov (United States)

    1992-01-01

    streptococcus faecalis ) in water. UV/ozone has been used for the breakdown of PCBs (33). A combination of UV, ozone and hydrogen peroxide is used in...quartz tube that was evacuated and then backfilled with oxygen. The samples were irradiated with UV light from a medium -pressure mercury lamp that...five percent of the output of these lamps is at 184.9-nm. Medium - and high-pressure UV lamps (17) generally have a much higher output in the short

  7. Surface ozone in the White Mountains of California

    Science.gov (United States)

    Joel Burley; Andrzej Bytnerowicz

    2011-01-01

    Surface ozone concentrations are presented for four high-elevation sites along a northesouth transect along the spine of the White Mountains and a fifth site located at lower elevation approximately 15 km to the west on the floor of the Owens Valley. The ozone data, which were collected from mid-June through mid-October of 2009, include results from two sites, White...

  8. 77 FR 58081 - Protection of Stratospheric Ozone: Listing of Substitutes for Ozone-Depleting Substances-Fire...

    Science.gov (United States)

    2012-09-19

    ... layer, avoiding adverse climate impacts, and result in human health and environmental benefits. List of... overall risk to human health and the environment than other available substitutes. In the ``Rules and... atmosphere are highly destructive to the stratospheric ozone layer. This action will provide users that need...

  9. Cosmic-Ray Reaction and Greenhouse Effect of Halogenated Molecules: Culprits for Atmospheric Ozone Depletion and Global Climate Change

    Science.gov (United States)

    Lu, Q.-B.

    2013-07-01

    This study is focused on the effects of cosmic rays (solar activity) and halogen-containing molecules (mainly chlorofluorocarbons — CFCs) on atmospheric ozone depletion and global climate change. Brief reviews are first given on the cosmic-ray-driven electron-induced-reaction (CRE) theory for O3 depletion and the warming theory of halogenated molecules for climate change. Then natural and anthropogenic contributions to these phenomena are examined in detail and separated well through in-depth statistical analyses of comprehensive measured datasets of quantities, including cosmic rays (CRs), total solar irradiance, sunspot number, halogenated gases (CFCs, CCl4 and HCFCs), CO2, total O3, lower stratospheric temperatures and global surface temperatures. For O3 depletion, it is shown that an analytical equation derived from the CRE theory reproduces well 11-year cyclic variations of both polar O3 loss and stratospheric cooling, and new statistical analyses of the CRE equation with observed data of total O3 and stratospheric temperature give high linear correlation coefficients ≥ 0.92. After the removal of the CR effect, a pronounced recovery by 20 25 % of the Antarctic O3 hole is found, while no recovery of O3 loss in mid-latitudes has been observed. These results show both the correctness and dominance of the CRE mechanism and the success of the Montreal Protocol. For global climate change, in-depth analyses of the observed data clearly show that the solar effect and human-made halogenated gases played the dominant role in Earth's climate change prior to and after 1970, respectively. Remarkably, a statistical analysis gives a nearly zero correlation coefficient (R = -0.05) between corrected global surface temperature data by removing the solar effect and CO2 concentration during 1850-1970. In striking contrast, a nearly perfect linear correlation with coefficients as high as 0.96-0.97 is found between corrected or uncorrected global surface temperature and total

  10. A climatological study of rural surface ozone in central Greece

    Directory of Open Access Journals (Sweden)

    P. D. Kalabokas

    2004-01-01

    Full Text Available Recent studies show that surface ozone levels at rural sites in Greece are generally high when compared with rural ozone measurements at northern European sites. The area of SE Europe, including Greece, is not very well monitored regarding rural ozone in comparison to central and northern Europe. In order to have the best possible picture of the rural surface ozone climatology in the area, based on the available data-sets of long-term continuous monitoring stations, the 10-year measurement records (1987-1996 of the Athens peripheral station of Liossia, (12 km N of the city center and the urban background station of Geoponiki (3 km W as well as the 4-year record (1996-1999 of the rural station of Aliartos (100 km NW of Athens, are analyzed in this paper. The data for Liossia and Geoponiki stations are screened for cases of strong airflow from rural areas (N-NE winds stronger than 5 m/s. The variation characteristics of the average rural ozone afternoon levels (12:00-18:00, with the best vertical atmospheric mixing, are mainly examined since these measurements are expected to be representative of the broader area. In all three stations there is a characteristic seasonal variation of rural ozone concentrations with lowest winter afternoon values at about 50 μg/m3 in December-January and average summer afternoon values at about 120 μg/m3 in July-August, indicating that high summer values are observed all over the area. The rural summer afternoon ozone values are very well correlated between the three stations, implying spatial homogeneity all over the area but also temporal homogeneity, since during the 13-year period 1987-1999 the rural afternoon ozone levels remained almost constant around the value of 120 μg/m3.

  11. Ozone threat

    International Nuclear Information System (INIS)

    Rajput, M.A.

    1995-01-01

    Ozone hole was first discovered in 1980. Thus 15 years even after the first warming, the world is no where near to the elimination of man made gases that threaten to destroy the ozone layer. Ozone depletion has become a matter of enormous threat which remains to be solved by the Scientists and intelligentia of the world. Ozone (O3) is a pungent poisonous gas. It forms a layer at a distance of about 15 miles above the earth's surface which helps shield living things from the sun shearing ultra violet light. If ozone is lost, more ultra violet light reaches the earth, which can lead to increasing rate of skin cancer, the death of micro organisms and the failure of crops and plants. It was in 1974 when it was discovered that Chlorofluorocarbons (CFCs) cold rise slowly to the upper atmosphere and destroy the earth's fragile ozone shield. Chlorofluorocarbons are commonly used as coolants (such as Freon) for home and automobile air conditioners and in the making of fast food containers. CFCs take about 100 years or more to reach he stratosphere to damage the ozone layers. In 1988, Scientists confirmed that upto 3% of the ozone layer over the more populated Northern Hemisphere has been destroyed. it is believed that for every 1% decrease in ozone, skin cancers are expected to rise 5 to 6 per cent due to the increase of ultraviolet light. Cases of cataracts and certain human immune system diseases are also expected to rise. (author)

  12. Stratospheric measurements of ozone-depleting substances and greenhouse gases using AirCores

    Science.gov (United States)

    Laube, Johannes; Leedham Elvidge, Emma; Kaiser, Jan; Sturges, Bill; Heikkinen, Pauli; Laurila, Tuomas; Hatakka, Juha; Kivi, Rigel; Chen, Huilin; Fraser, Paul; van der Veen, Carina; Röckmann, Thomas

    2017-04-01

    Retrieving air samples from the stratosphere has previously required aircraft or large balloons, both of which are expensive to operate. The novel "AirCore" technique (Karion et al., 2010) enables stratospheric sampling using weather balloons, which is much more cost effective. AirCores are long (up to 200 m) stainless steel tubes which are placed as a payload on a small balloon, can ascend to over 30 km and fill upon descent, collecting a vertical profile of the atmosphere. Retrieved volumes are much smaller though, which presents a challenge for trace gas analysis. To date, only the more abundant trace gases such as carnon dioxide (CO2) and methane (CH4) have been quantified in AirCores. Halogenated trace gases are also important greenhouse gases and many also deplete stratospheric ozone. Their concentrations are however much lower i.e. typically in the part per trillion (ppt) molar range. We here present the first stratospheric measurements of halocarbons in AirCores obtained using UEA's highly sensitive (detection limits of 0.01-0.1 ppt in 10 ml of air) gas chromatography mass spectrometry system. The analysed air originates from a Stratospheric Air Sub-sampler (Mrozek et al., 2016) which collects AirCore segments after the non-destructive CO2 and CH4 analysis. Successfully measured species include CFC-11, CFC-12, CFC-113, CFC-115, H-1211, H-1301, HCFC-22, HCFC-141b, HCFC-142b, HCFC-133a, and sulphur hexafluoride (SF6). We compare the observed mixing ratios and precisions with data obtained from samples collected during various high-altitude aircraft campaigns between 2009 and 2016 as well as with southern hemisphere tropospheric long-term trends. As part of the ERC-funded EXC3ITE (EXploring stratospheric Composition, Chemistry and Circulation with Innovative Techniques) project more than 40 AirCore flights are planned in the next 3 years with an expanded range of up to 30 gases in order to explore seasonal and interannual variability in the stratosphere

  13. Next Generation Refrigeration Lubricants for Low Global Warming Potential/Low Ozone Depleting Refrigeration and Air Conditioning Systems

    Energy Technology Data Exchange (ETDEWEB)

    Hessell, Edward Thomas [Chemtura Corporation, Middlebury, CT (United States)

    2013-12-31

    The goal of this project is to develop and test new synthetic lubricants that possess high compatibility with new low ozone depleting (LOD) and low global warming potential (LGWP) refrigerants and offer improved lubricity and wear protection over current lubricant technologies. The improved compatibility of the lubricants with the refrigerants, along with improved lubricating properties, will resulted in lower energy consumption and longer service life of the refrigeration systems used in residential, commercial and industrial heating, ventilating and air-conditioning (HVAC) and refrigeration equipment.

  14. Degradation and toxicity depletion of RB19 anthraquinone dye in water by ozone-based technologies.

    Science.gov (United States)

    Lovato, María E; Fiasconaro, María L; Martín, Carlos A

    2017-02-01

    This research investigated the discoloration and mineralization of Reactive Blue 19 (RB19) anthraquinone dye by single ozonation, single UV radiation and ozonation jointed with UV radiation (O 3 /UV). The problem was approached from two points of view: with the objective of color removal or the mineralization of solution. In each case, the optimum operating conditions were different. Ozonation was the most effective treatment for color removal, while the combined O 3 /UV treatment was for mineralization. Major intermediates of the dye degradation were identified by gas chromatography/mass spectrometry and a degradation pathway was proposed. In addition, a clear decrease of the toxicity of the dye was achieved at the end of the experiments. The effect of initial dye concentration, pH, ozone dose, and UV radiation on the degradation of the dye and decrease of total organic carbon was investigated, in order to establish the optimal operating conditions to achieve discoloration, mineralization or a combination of both.

  15. Variability of surface ozone with cloud coverage over Kolkata, India

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Earth System Science; Volume 124; Issue 2. Variability of surface ozone with cloud coverage over Kolkata, India. D Ghosh ... Engineering, Jadavpur University, Jadavpur, Kolkata 700 032, India. Department of Atmospheric Sciences, Calcutta University, 92, A.P.C. Road, Kolkata 700 009, India.

  16. Trends in total column ozone over Australia and New Zealand and its influence on clear-sky surface erythemal irradiance

    International Nuclear Information System (INIS)

    Bodeker, G. E.

    1995-01-01

    Australia and New Zealand are two of the countries closest to the Antarctic ozone depletion and may therefore be 'at risk' as a result of the associated increases in surface ultraviolet (UV) radiation. To investigate the possible impact of mid-latitude ozone decreases on surface erythemal irradiances, monthly mean total ozone has been calculated from daily total ozone mapping spectrometer data for 5 Australian cities (Canberra, Hobart, Melbourne, Perth and Sydney) and 3 New Zealand cities (Auckland, Christchurch and Wellington) from 1979 to 1992. These values have then been used as inputs to a single layer model to calculate noon clear-sky global UV irradiances and associated erythemal irradiances. In addition, the monthly mean ozone data have been modelled statistically for each location to reveal a long-term linear trend, an annual variation, a Quasi-Biennial Oscillation (QBO), a solar cycle component and a semi-annual (6 month) signal. Coefficients from these statistical models have been used to estimate monthly mean ozone and noon clear-sky erythemal irradiances to the year 2000 for each city. It is assumed that the rate of increase of stratospheric chlorine over the remainder of the century will remain constant. Given that there is some evidence that the rate of increase is decreasing, the results present here should be regarded as an upper limit. 33 refs., 7 tabs., 4 figs

  17. Will climate change increase ozone depletion from low-energy-electron precipitation?

    Directory of Open Access Journals (Sweden)

    A. J. G. Baumgaertner

    2010-10-01

    Full Text Available We investigate the effects of a strengthened stratospheric/mesospheric residual circulation on the transport of nitric oxide (NO produced by energetic particle precipitation. During periods of high geomagnetic activity, energetic electron precipitation (EEP is responsible for winter time ozone loss in the polar middle atmosphere between 1 and 6 hPa. However, as climate change is expected to increase the strength of the Brewer-Dobson circulation including extratropical downwelling, the enhancements of EEP NOx concentrations are expected to be transported to lower altitudes in extratropical regions, becoming more significant in the ozone budget. Changes in the mesospheric residual circulation are also considered. We use simulations with the chemistry climate model system EMAC to compare present day effects of EEP NOx with expected effects in a climate change scenario for the year 2100. In years of strong geomagnetic activity, similar to that observed in 2003, an additional polar ozone loss of up to 0.4 μmol/mol at 5 hPa is found in the Southern Hemisphere. However, this would be approximately compensated by an ozone enhancement originating from a stronger poleward transport of ozone from lower latitudes caused by a strengthened Brewer-Dobson circulation, as well as by slower photochemical ozone loss reactions in a stratosphere cooled by risen greenhouse gas concentrations. In the Northern Hemisphere the EEP NOx effect appears to lose importance due to the different nature of the climate-change induced circulation changes.

  18. The impacts of surface ozone pollution on winter wheat productivity in China--An econometric approach.

    Science.gov (United States)

    Yi, Fujin; Jiang, Fei; Zhong, Funing; Zhou, Xun; Ding, Aijun

    2016-01-01

    The impact of surface ozone pollution on winter wheat yield is empirically estimated by considering socio-economic and weather determinants. This research is the first to use an economic framework to estimate the ozone impact, and a unique county-level panel is employed to examine the impact of the increasing surface ozone concentration on the productivity of winter wheat in China. In general, the increment of surface ozone concentration during the ozone-sensitive period of winter wheat is determined to be harmful to its yield, and a conservative reduction of ozone pollution could significantly increase China's wheat supply. Copyright © 2015 Elsevier Ltd. All rights reserved.

  19. Atmospheric chemistry of short-chain haloolefins: photochemical ozone creation potentials (POCPs), global warming potentials (GWPs), and ozone depletion potentials (ODPs).

    Science.gov (United States)

    Wallington, T J; Sulbaek Andersen, M P; Nielsen, O J

    2015-06-01

    Short-chain haloolefins are being introduced as replacements for saturated halocarbons. The unifying chemical feature of haloolefins is the presence of a CC double bond which causes the atmospheric lifetimes to be significantly shorter than for the analogous saturated compounds. We discuss the atmospheric lifetimes, photochemical ozone creation potentials (POCPs), global warming potentials (GWPs), and ozone depletion potentials (ODPs) of haloolefins. The commercially relevant short-chain haloolefins CF3CFCH2 (1234yf), trans-CF3CHCHF (1234ze(Z)), CF3CFCF2 (1216), cis-CF3CHCHCl (1233zd(Z)), and trans-CF3CHCHCl (1233zd(E)) have short atmospheric lifetimes (days to weeks), negligible POCPs, negligible GWPs, and ODPs which do not differ materially from zero. In the concentrations expected in the environment their atmospheric degradation products will have a negligible impact on ecosystems. CF3CFCH2 (1234yf), trans-CF3CHCHF (1234ze(Z)), CF3CFCF2 (1216), cis-CF3CHCHCl (1233zd(Z)), and trans-CF3CHCHCl (1233zd(E)) are environmentally acceptable. Copyright © 2015 Elsevier Ltd. All rights reserved.

  20. Environmental effects of ozone depletion and its interactions with climate change: Progress report, 2016

    Science.gov (United States)

    When considering the effects of climate change, it has become clear that processes resulting in changes in stratospheric ozone are more complex than previously believed. As a result of this, human health and environmental issues will be longer-lasting and more regionally variable...

  1. Uncertainties in modelling heterogeneous chemistry and Arctic ozone depletion in the winter 2009/2010

    Directory of Open Access Journals (Sweden)

    I. Wohltmann

    2013-04-01

    Full Text Available Stratospheric chemistry and denitrification are simulated for the Arctic winter 2009/2010 with the Lagrangian Chemistry and Transport Model ATLAS. A number of sensitivity runs is used to explore the impact of uncertainties in chlorine activation and denitrification on the model results. In particular, the efficiency of chlorine activation on different types of liquid aerosol versus activation on nitric acid trihydrate clouds is examined. Additionally, the impact of changes in reaction rate coefficients, in the particle number density of polar stratospheric clouds, in supersaturation, temperature or the extent of denitrification is investigated. Results are compared to satellite measurements of MLS and ACE-FTS and to in-situ measurements onboard the Geophysica aircraft during the RECONCILE measurement campaign. It is shown that even large changes in the underlying assumptions have only a small impact on the modelled ozone loss, even though they can cause considerable differences in chemical evolution of other species and in denitrification. Differences in column ozone between the sensitivity runs stay below 10% at the end of the winter. Chlorine activation on liquid aerosols alone is able to explain the observed magnitude and morphology of the mixing ratios of active chlorine, reservoir gases and ozone. This is even true for binary aerosols (no uptake of HNO3 from the gas-phase allowed in the model. Differences in chlorine activation between sensitivity runs are within 30%. Current estimates of nitric acid trihydrate (NAT number density and supersaturation imply that, at least for this winter, NAT clouds play a relatively small role compared to liquid clouds in chlorine activation. The change between different reaction rate coefficients for liquid or solid clouds has only a minor impact on ozone loss and chlorine activation in our sensitivity runs.

  2. Seasonal changes in surface ozone over South Korea

    Directory of Open Access Journals (Sweden)

    Hyun-Chae Jung

    2018-01-01

    Full Text Available Recently, the surface ozone concentration in the Korean peninsula has been increasing more rapidly than in the past, and seasonal changes are appearing such as increases in the number of ozone alerts in springtime. We examined changes in the timing of annual maximum South Korean O3 levels by fitting a sine function to data from 54 air-quality monitoring sites over a 10-year period (2005–2014. The analytical results show that the date of maximum ozone concentration at 23 points in the last 10 years has been advanced by about 2.1 days per year (E-sites, while the remaining 31 points have been delayed by about 2.5 days per year (L-sites. We attribute these differences to seasonal O3 changes: E-sites show a larger increase in O3 level in March–April (MA than in June–July (JJ, while L-sites show a larger increase in JJ than in MA. Furthermore, these shifts are significantly larger in magnitude than those reported for Europe and North America. We also examined one possible reason for these seasonal differences: the relationship between O3 and precursors such as NO2 and CO. E-sites showed a rapid decrease in NO2 (NO concentration in MA over the last decade. As a result, the ozone concentration at E-sites seems to have increased due to the absence of ozone destruction by NOx titration in early spring. In L-Sites, the concentrations of ozone precursors such as NO2 and CO in JJ showed a smaller decrease than those at other sites. Therefore, in L-sites, relatively large amounts of ozone precursors were distributed in JJ, implying that more ozone was generated. We suggest that shifts in the South Korean O3 seasonal cycle are due to changes in early spring and summer NO2 (NO and CO levels; this should be tested further by modeling studies.

  3. The GEOS Chemistry Climate Model: Implications of Climate Feedbacks on Ozone Depletion and Recovery

    Science.gov (United States)

    Stolarski, Richard S.; Pawson, Steven; Douglass, Anne R.; Newman, Paul A.; Kawa, S. Randy; Nielsen, J. Eric; Rodriquez, Jose; Strahan, Susan; Oman, Luke; Waugh, Darryn

    2008-01-01

    The Goddard Earth Observing System Chemistry Climate Model (GEOS CCM) has been developed by combining the atmospheric chemistry and transport modules developed over the years at Goddard and the GEOS general circulation model, also developed at Goddard. The first version of the model was used in the CCMVal intercomparison exercises that contributed to the 2006 WMO/UNEP Ozone Assessment. The second version incorporates the updated version of the GCM (GEOS 5) and will be used for the next round of CCMVal evaluations and the 2010 Ozone Assessment. The third version, now under development, incorporates the combined stratosphere and troposphere chemistry package developed under the Global Modeling Initiative (GMI). We will show comparison to past observations that indicate that we represent the ozone trends over the past 30 years. We will also show the basic temperature, composition, and dynamical structure of the simulations. We will further show projections into the future. We will show results from an ensemble of transient and time-slice simulations, including simulations with fixed 1960 chlorine, simulations with a best guess scenario (Al), and simulations with extremely high chlorine loadings. We will discuss planned extensions of the model to include emission-based boundary conditions for both anthropogenic and biogenic compounds.

  4. Subsidence of aircraft engine exhaust in the stratosphere: Implications for calculated ozone depletions

    Science.gov (United States)

    Rodriguez, J. M.; Shia, R.-L.; Ko, M. K. W.; Heisey, C. W.; Weistenstein, D. K.; Miake-Lye, R. C.; Kolb, C. E.

    1994-01-01

    The deposition altitude of nitrogen oxides and other exhaust species emitted by stratospheric aircraft is a crucial parameter in determining the impact of these emissions on stratospheric ozone. We have utilized a model for the wake of a High-Speed Civil Transport (HSCT) to estimate the enhancements in water and reductions in ozone in these wakes as a function of time. Radiative calculations indicate differential cooling rates as large as -5K/day at the beginning of the far-wake regime, mostly due to the enhanced water abundance. These cooling rates would imply a net sinking of the wakes of about 1.2 km after three days in the limit of no mixing. Calculated mid-latitude column ozone reductions due to emissions from a Mach 2.4 HSCT would then change from about -1% to -06%. However, more realistic calculations adopting moderate mixing for the wake reduce the net sinking to less than 0.2 km, making the impact of radiative subsidence negligible.

  5. Atmospheric lifetimes and ozone depletion potentials of methyl bromide (CH3Br) and dibromomethane (CH2Br2)

    Energy Technology Data Exchange (ETDEWEB)

    Mellouki, A.; Talukdar, R.K.; Schmoltner, A.; Gierczak, T.; Mills, M.J.; Solomon, S.; Ravishankara, A.R. (NOAA, Boulder, CO (United States))

    1992-10-01

    The rate coefficients for the reactions of OH radical with CH3Br and CH2Br2 were measured as functions of temperature using the laser photolysis - laser induced fluorescence method. This data was incorporated into a semiempirical model (Solomon et al., 1992) and a 2D model to calculate the steady-state ozone depletion potentials (ODP) and atmospheri lifetimes, tau, with greatly improved accuracy as compared to earlier studies. The calculated ODPs and tau are 0.65 and 1.7 years and 0.17 and 0.41 years for CH3Br and CH2Br2, respectively, using the semiempirical model. These lifetimes agree well with those calculated using a 2D model. This study better quantifies the ODPs and tau of these species which are needed inputs for discussion of possible regulation of human emissions currently under international considerations. 29 refs.

  6. Ozone-surface reactions in five homes: surface reaction probabilities, aldehyde yields, and trends.

    Science.gov (United States)

    Wang, H; Morrison, G

    2010-06-01

    Field experiments were conducted in five homes during three seasons (summer 2005, summer 2006 and winter 2007) to quantify ozone-initiated secondary aldehyde yields, surface reaction probabilities, and trends any temporal over a 1.5-year interval. Surfaces examined include living room carpets, bedroom carpets, kitchen floors, kitchen counters, and living room walls. Reaction probabilities for all surfaces for all seasons ranged from 9.4 x 10(-8) to 1.0 x 10(-4). There were no significant temporal trends in reaction probabilities for any surfaces from summer 2005 to summer 2006, nor over the entire 1.5-year period, indicating that it may take significantly longer than this period for surfaces to exhibit any 'ozone aging' or lowering of ozone-surface reactivity. However, all surfaces in three houses exhibited a significant decrease in reaction probabilities from summer 2006 to winter 2007. The total yield of aldehydes for the summer of 2005 were nearly identical to that for summer of 2006, but were significantly higher than for winter 2007. We also observed that older carpets were consistently less reactive than in newer carpets, but that countertops remained consistently reactive, probably because of occupant activities such as cooking and cleaning. Ozone reactions taking place at indoor surfaces significantly influence personal exposure to ozone and volatile reaction products. These field studies show that indoor surfaces only slowly lose their ability to react with ozone over several year time frames, and that this is probably because of a combination of large reservoirs of reactive coatings and periodic additions of reactive coatings in the form of cooking, cleaning, and skin-oil residues. When considering exposure to ozone and its reaction products and in the absence of dramatic changes in occupancy, activities or furnishings, indoor surface reactivity is expected to change very slowly.

  7. A Three-Tier Diagnostic Test to Assess Pre-Service Teachers' Misconceptions about Global Warming, Greenhouse Effect, Ozone Layer Depletion, and Acid Rain

    Science.gov (United States)

    Arslan, Harika Ozge; Cigdemoglu, Ceyhan; Moseley, Christine

    2012-01-01

    This study describes the development and validation of a three-tier multiple-choice diagnostic test, the atmosphere-related environmental problems diagnostic test (AREPDiT), to reveal common misconceptions of global warming (GW), greenhouse effect (GE), ozone layer depletion (OLD), and acid rain (AR). The development of a two-tier diagnostic test…

  8. The Nature of Relationships among the Components of Pedagogical Content Knowledge of Preservice Science Teachers: "Ozone Layer Depletion" as an Example

    Science.gov (United States)

    Kaya, Osman N.

    2009-01-01

    The purpose of this study was to explore the relationships among the components of preservice science teachers' (PSTs) pedagogical content knowledge (PCK) involving the topic "ozone layer depletion". An open-ended survey was first administered to 216 PSTs in their final year at the Faculty of Education to determine their subject matter…

  9. Students' Understanding of the Greenhouse Effect, the Societal Consequences of Reducing CO2 Emissions and the Problem of Ozone Layer Depletion.

    Science.gov (United States)

    Andersson, Bjorn; Wallin, Anita

    2000-01-01

    Contributes to the growing body of knowledge about students' conceptions and views of environmental and natural resource issues. Questions 9th and 12th grade Swedish students' understandings of the greenhouse effect, reduction of CO2 emissions, and the depletion of the ozone layer. Observes five models of the greenhouse effect that appear among…

  10. Concept Formation in Environmental Education: 14-Year Olds' Work on the Intensified Greenhouse Effect and the Depletion of the Ozone Layer. Research Report

    Science.gov (United States)

    Osterlind, Karolina

    2005-01-01

    A case study is presented describing the work of three pupils in the upper level of compulsory school. The pupils were learning about the intensified greenhouse effect and the depletion of the ozone layer. In their work, the need for certain domain-specific knowledge becomes apparent; for example, understanding such concepts as photosynthesis,…

  11. Ozone treatment and the depletion of detectable pharmaceuticals and atrazine herbicide in drinking water sourced from the upper Detroit River, Ontario, Canada.

    Science.gov (United States)

    Hua, Wenyi; Bennett, Erin R; Letcher, Robert J

    2006-07-01

    The depletion and degradation of pharmacologically active compounds (PhACs) and pesticides as a function of ozonation in drinking water treatment processes is not well studied. The A.H. Weeks drinking water treatment plant (DWTP) serves the City of Windsor, Ontario Canada, and incorporates ozone treatment into the production of drinking water. This DWTP also operates a real-time, scaled down pilot plant, which has two parallel streams, conventional and ozone plus conventional treatments. In this study water samples were collected from key points in the two streams of the pilot plant system to determine the depletion and influence of seasonal changes in water processing parameters on eighteen major PhACs (and metabolites) and seven s-triazines herbicides. However, only carbamazepine (antiepileptic), caffeine (stimulant), cotinine (metabolite of nicotine) and atrazine were consistently detectable in the raw water intake (low to sub-ng/L level). Regardless of the seasonality, the flocculation-coagulation and dual media filtration steps without ozone treatment resulted in no decrease in analyte concentrations, while decreases of 66-100% (undetectable, method detection limits 0.05-1 ng/L) of the analyte concentrations were observed when ozone treatment was part of the water processing. These findings demonstrate that ozone treatment is highly effective in depleting carbamazepine, caffeine, cotinine, and atrazine, and thus is highly influential in the fate of these compounds in drinking water treatment regardless of the seasonal time frame. Currently very few Canadian DWTPs incorporate ozonation into conventional treatment, which suggests that human exposure to these compounds via drinking water consumption may be an issue in affected communities.

  12. Electrochemical corrosion behaviours of pulsed bias MSIP aluminum coating on depleted uranium surface

    International Nuclear Information System (INIS)

    Wang Qingfu; Zhang Pengcheng; Chen Lin; Liu Qinghe; Lang Dingmu; Wang Xiaohong

    2009-01-01

    Aluminum coating was prepared by magnetron sputtering ion plating (MSIP) with pulsed bias on depleted uranium surface. Its electrochemical corrosion behaviours were studied by electrochemical technology, scanning electron microscope (SEM) and X-ray energy dispersive spectroscope (EDS). The corrosion potential of aluminum coating (-534.8 mV) is higher than that of depleted uranium (-641.2 mV). The aluminum coating is a cathodic deposit to depleted uranium. Depleted uranium coated aluminum has much higher polarization resistance,greater magnitude of electrochemical impedance and much lower corrosion current than that of depleted uranium. The aluminum coating has a good corrosion resistance to depleted uranium. Corrosion characteristic of depleted uranium coated aluminum is a typical local corrosion. Meanwhile,the aluminum coating cracks and flakes off from depleted uranium substrate, which deteriorates its anti-corrosion property. Pseudo-diffusion layer on interface between aluminum coating and uranium substrate has some degree of anti-corrosion effect. (authors)

  13. The Hole in the Ozone Layer.

    Science.gov (United States)

    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.…

  14. Relationship between surface, free tropospheric and total column ozone in 2 contrasting areas in South-Africa

    CSIR Research Space (South Africa)

    Combrink, J

    1995-04-01

    Full Text Available Measurements of surface ozone in two contrasting areas of South Africa are compared with free tropospheric and Total Ozone Mapping Spectrometer (TOMS) total column ozone data. Cape Point is representative of a background monitoring station which...

  15. Analysis of reactive bromine production and ozone depletion in the Arctic boundary layer using 3-D simulations with GEM-AQ: inference from synoptic-scale patterns

    Science.gov (United States)

    Toyota, K.; McConnell, J. C.; Lupu, A.; Neary, L.; McLinden, C. A.; Richter, A.; Kwok, R.; Semeniuk, K.; Kaminski, J. W.; Gong, S.-L.; Jarosz, J.; Chipperfield, M. P.; Sioris, C. E.

    2011-04-01

    Episodes of high bromine levels and surface ozone depletion in the springtime Arctic are simulated by an online air-quality model, GEM-AQ, with gas-phase and heterogeneous reactions of inorganic bromine species and a simple scheme of air-snowpack chemical interactions implemented for this study. Snowpack on sea ice is assumed to be the only source of bromine to the atmosphere and to be capable of converting relatively stable bromine species to photolabile Br2 via air-snowpack interactions. A set of sensitivity model runs are performed for April 2001 at a horizontal resolution of approximately 100 km×100 km in the Arctic, to provide insights into the effects of temperature and the age (first-year, FY, versus multi-year, MY) of sea ice on the release of reactive bromine to the atmosphere. The model simulations capture much of the temporal variations in surface ozone mixing ratios as observed at stations in the high Arctic and the synoptic-scale evolution of areas with enhanced BrO column amount ("BrO clouds") as estimated from satellite observations. The simulated "BrO clouds" are in modestly better agreement with the satellite measurements when the FY sea ice is assumed to be more efficient at releasing reactive bromine to the atmosphere than on the MY sea ice. Surface ozone data from coastal stations used in this study are not sufficient to evaluate unambiguously the difference between the FY sea ice and the MY sea ice as a source of bromine. The results strongly suggest that reactive bromine is released ubiquitously from the snow on the sea ice during the Arctic spring while the timing and location of the bromine release are largely controlled by meteorological factors. It appears that a rapid advection and an enhanced turbulent diffusion associated with strong boundary-layer winds drive transport and dispersion of ozone to the near-surface air over the sea ice, increasing the oxidation rate of bromide (Br-) in the surface snow. Also, if indeed the surface

  16. Analysis of reactive bromine production and ozone depletion in the Arctic boundary layer using 3-D simulations with GEM-AQ: inference from synoptic-scale patterns

    Directory of Open Access Journals (Sweden)

    K. Toyota

    2011-04-01

    Full Text Available Episodes of high bromine levels and surface ozone depletion in the springtime Arctic are simulated by an online air-quality model, GEM-AQ, with gas-phase and heterogeneous reactions of inorganic bromine species and a simple scheme of air-snowpack chemical interactions implemented for this study. Snowpack on sea ice is assumed to be the only source of bromine to the atmosphere and to be capable of converting relatively stable bromine species to photolabile Br2 via air-snowpack interactions. A set of sensitivity model runs are performed for April 2001 at a horizontal resolution of approximately 100 km×100 km in the Arctic, to provide insights into the effects of temperature and the age (first-year, FY, versus multi-year, MY of sea ice on the release of reactive bromine to the atmosphere. The model simulations capture much of the temporal variations in surface ozone mixing ratios as observed at stations in the high Arctic and the synoptic-scale evolution of areas with enhanced BrO column amount ("BrO clouds" as estimated from satellite observations. The simulated "BrO clouds" are in modestly better agreement with the satellite measurements when the FY sea ice is assumed to be more efficient at releasing reactive bromine to the atmosphere than on the MY sea ice. Surface ozone data from coastal stations used in this study are not sufficient to evaluate unambiguously the difference between the FY sea ice and the MY sea ice as a source of bromine. The results strongly suggest that reactive bromine is released ubiquitously from the snow on the sea ice during the Arctic spring while the timing and location of the bromine release are largely controlled by meteorological factors. It appears that a rapid advection and an enhanced turbulent diffusion associated with strong boundary-layer winds drive transport and dispersion of ozone to the near-surface air over the sea ice, increasing the oxidation rate of bromide (Br in the surface

  17. Surface ozone scenario at Pune and Delhi during the decade of 1990s

    Indian Academy of Sciences (India)

    Transport mechanism is also understood to have contributed significantly to the total concentration of ozone. Inverse relationship obtained between surface ozone concentration and relative humidity indicates that major photochemical paths for removal of ozone become effective when humidity increases at these locations.

  18. The impacts of surface ozone pollution on winter wheat productivity in China – An econometric approach

    International Nuclear Information System (INIS)

    Yi, Fujin; Jiang, Fei; Zhong, Funing; Zhou, Xun; Ding, Aijun

    2016-01-01

    The impact of surface ozone pollution on winter wheat yield is empirically estimated by considering socio-economic and weather determinants. This research is the first to use an economic framework to estimate the ozone impact, and a unique county-level panel is employed to examine the impact of the increasing surface ozone concentration on the productivity of winter wheat in China. In general, the increment of surface ozone concentration during the ozone-sensitive period of winter wheat is determined to be harmful to its yield, and a conservative reduction of ozone pollution could significantly increase China's wheat supply. - Highlights: • We examine the impacts of the surface ozone exposure on winter wheat yield in China. • An econometric method is used to measure the ozone impacts. • The results conclude that surface ozone is harmful to winter wheat yield in China. • We confirm that stress conditions such as drought and air particles can mitigate the adverse effect of ozone. - Surface ozone pollution is harmful to winter wheat yield in China by considering socio-economic determinants, weather, and other stress conditions like drought and air particles.

  19. Changes in air quality and tropospheric composition due to depletion of stratospheric ozone and interactions with climate.

    Science.gov (United States)

    Tang, X; Wilson, S R; Solomon, K R; Shao, M; Madronich, S

    2011-02-01

    , meteorological conditions, and anthropogenic emissions may be large, thus posing challenges for prediction and management of air quality. Aerosols composed of organic substances have a major role in both climate and air quality, and contribute a large uncertainty to the energy budget of the atmosphere. These aerosols are mostly formed via the UV-initiated oxidation of VOCs from anthropogenic and biogenic sources, although the details of the chemistry are still poorly understood and current models under-predict their abundance. A better understanding of their formation, chemical composition, and optical properties is required to assess their significance for air quality and to better quantify their direct and indirect radiative forcing of climate. Emissions of compounds containing fluorine will continue to have effects on the chemistry of the atmosphere and on climate change. The HCFCs and HFCs used as substitutes for ozone-depleting CFCs can break down into trifluoroacetic acid (TFA), which will accumulate in oceans, salt lakes, and playas. Based on historical use and projections of future uses, including new products entering the market, such as the fluoro-olefins, increased loadings of TFA in these environmental sinks will be small. Even when added to existing amounts from natural sources, risks to humans or the environment from the historical use of CFCs or continued use of their replacements is judged to be negligible.

  20. Environmental effects of ozone depletion, UV radiation and interactions with climate change: UNEP Environmental Effects Assessment Panel, update 2017.

    Science.gov (United States)

    Bais, A F; Lucas, R M; Bornman, J F; Williamson, C E; Sulzberger, B; Austin, A T; Wilson, S R; Andrady, A L; Bernhard, G; McKenzie, R L; Aucamp, P J; Madronich, S; Neale, R E; Yazar, S; Young, A R; de Gruijl, F R; Norval, M; Takizawa, Y; Barnes, P W; Robson, T M; Robinson, S A; Ballaré, C L; Flint, S D; Neale, P J; Hylander, S; Rose, K C; Wängberg, S-Å; Häder, D-P; Worrest, R C; Zepp, R G; Paul, N D; Cory, R M; Solomon, K R; Longstreth, J; Pandey, K K; Redhwi, H H; Torikai, A; Heikkilä, A M

    2018-02-14

    The Environmental Effects Assessment Panel (EEAP) is one of three Panels of experts that inform the Parties to the Montreal Protocol. The EEAP focuses on the effects of UV radiation on human health, terrestrial and aquatic ecosystems, air quality, and materials, as well as on the interactive effects of UV radiation and global climate change. When considering the effects of climate change, it has become clear that processes resulting in changes in stratospheric ozone are more complex than previously held. Because of the Montreal Protocol, there are now indications of the beginnings of a recovery of stratospheric ozone, although the time required to reach levels like those before the 1960s is still uncertain, particularly as the effects of stratospheric ozone on climate change and vice versa, are not yet fully understood. Some regions will likely receive enhanced levels of UV radiation, while other areas will likely experience a reduction in UV radiation as ozone- and climate-driven changes affect the amounts of UV radiation reaching the Earth's surface. Like the other Panels, the EEAP produces detailed Quadrennial Reports every four years; the most recent was published as a series of seven papers in 2015 (Photochem. Photobiol. Sci., 2015, 14, 1-184). In the years in between, the EEAP produces less detailed and shorter Update Reports of recent and relevant scientific findings. The most recent of these was for 2016 (Photochem. Photobiol. Sci., 2017, 16, 107-145). The present 2017 Update Report assesses some of the highlights and new insights about the interactive nature of the direct and indirect effects of UV radiation, atmospheric processes, and climate change. A full 2018 Quadrennial Assessment, will be made available in 2018/2019.

  1. Ozone Oxidation of Self-Assembled Monolayers on SiOx-Coated Zinc Selenide Surfaces

    Science.gov (United States)

    McIntire, T. M.; Ryder, O. S.; Finlayson-Pitts, B. J.

    2008-12-01

    Airborne particles are important for visibility, human health, climate, and atmospheric reactions. Atmospheric particles contain a significant fraction of organics and such compounds present on airborne particles are susceptible to oxidation by atmospheric oxidants, such as OH, ozone, halogen atoms, and nitrogen trioxide. Oxidized organics associated with airborne particles are thought to be polar, hygroscopic species with enhanced cloud-nucleating properties. Oxide layers on silicon, or SiO2-coated substrates, act as models of environmentally relevant surfaces such as dust particles upon which organics adsorb. We have shown previously that ozone oxidation of unsaturated self-assembled monolayers (SAMs) on silicon attenuated total reflectance (ATR) crystals leads to the formation of carbonyl groups and micron-sized, hydrophobic organic aggregates surrounded by carbon depleted substrate that do not have increased water uptake as previously assumed. Reported here are further ATR-FTIR studies of the oxidation of alkene SAMs on ZnSe and SiO2-coated ZnSe. These substrates have the advantage that they transmit below 1500 cm-1, allowing detection of additional product species. These experiments show that the loss of C=C and formation of carbonyl groups is also accompanied by formation of a peak at 1110 cm-1, attributed to the secondary ozonide. Details concerning the products and mechanism of ozonolysis of alkene SAMs on surfaces based on these new data are presented and the implications for the oxidation of alkenes on airborne dust particles are discussed.

  2. Environmental effects of ozone depletion and its interactions with climate change: Progress report, 2016.

    Science.gov (United States)

    2017-02-15

    The Parties to the Montreal Protocol are informed by three Panels of experts. One of these is the Environmental Effects Assessment Panel (EEAP), which deals with two focal issues. The first focus is the effects of UV radiation on human health, animals, plants, biogeochemistry, air quality, and materials. The second focus is on interactions between UV radiation and global climate change and how these may affect humans and the environment. When considering the effects of climate change, it has become clear that processes resulting in changes in stratospheric ozone are more complex than previously believed. As a result of this, human health and environmental issues will be longer-lasting and more regionally variable. Like the other Panels, the EEAP produces a detailed report every four years; the most recent was published as a series of seven papers in 2015 (Photochem. Photobiol. Sci., 2015, 14, 1-184). In the years in between, the EEAP produces less detailed and shorter Progress Reports of the relevant scientific findings. The most recent of these was for 2015 (Photochem. Photobiol. Sci., 2016, 15, 141-147). The present Progress Report for 2016 assesses some of the highlights and new insights with regard to the interactive nature of the direct and indirect effects of UV radiation, atmospheric processes, and climate change. The more detailed Quadrennial Assessment will be made available in 2018.

  3. Possible role of electric forces in bromine activation during polar boundary layer ozone depletion and aerosol formation events

    Science.gov (United States)

    Tkachenko, Ekaterina

    2017-11-01

    This work presents a hypothesis about the mechanism of bromine activation during polar boundary layer ozone depletion events (ODEs) as well as the mechanism of aerosol formation from the frost flowers. The author suggests that ODEs may be initiated by the electric-field gradients created at the sharp tips of ice formations as a result of the combined effect of various environmental conditions. According to the author's estimates, these electric-field gradients may be sufficient for the onset of point or corona discharges followed by generation of high local concentrations of the reactive oxygen species and initiation of free-radical and redox reactions. This process may be responsible for the formation of seed bromine which then undergoes further amplification by HOBr-driven bromine explosion. The proposed hypothesis may explain a variety of environmental conditions and substrates as well as poor reproducibility of ODE initiation observed by researchers in the field. According to the author's estimates, high wind can generate sufficient conditions for overcoming the Rayleigh limit and thus can initiate ;spraying; of charged aerosol nanoparticles. These charged aerosol nanoparticles can provoke formation of free radicals, turning the ODE on. One can also envision a possible emission of halogen ion as a result of the ;electrospray; process analogous to that of electrospray ionization mass-spectrometry.

  4. Extreme ozone depletion in the 2010–2011 Arctic winter stratosphere as observed by MIPAS/ENVISAT using a 2-D tomographic approach

    Directory of Open Access Journals (Sweden)

    E. Arnone

    2012-10-01

    Full Text Available We present observations of the 2010–2011 Arctic winter stratosphere from the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS onboard ENVISAT. Limb sounding infrared measurements were taken by MIPAS during the Northern polar winter and into the subsequent spring, giving a continuous vertically resolved view of the Arctic dynamics, chemistry and polar stratospheric clouds (PSCs. We adopted a 2-D tomographic retrieval approach to account for the strong horizontal inhomogeneity of the atmosphere present under vortex conditions, self-consistently comparing 2011 to the 2-D analysis of 2003–2010. Unlike most Arctic winters, 2011 was characterized by a strong stratospheric vortex lasting until early April. Lower stratospheric temperatures persistently remained below the threshold for PSC formation, extending the PSC season up to mid-March, resulting in significant chlorine activation leading to ozone destruction. On 3 January 2011, PSCs were detected up to 30.5 ± 0.9 km altitude, representing the highest PSCs ever reported in the Arctic. Through inspection of MIPAS spectra, 83% of PSCs were identified as supercooled ternary solution (STS or STS mixed with nitric acid trihydrate (NAT, 17% formed mostly by NAT particles, and only two cases by ice. In the lower stratosphere at potential temperature 450 K, vortex average ozone showed a daily depletion rate reaching 100 ppbv day−1. In early April at 18 km altitude, 10% of vortex measurements displayed total depletion of ozone, and vortex average values dropped to 0.6 ppmv. This corresponds to a chemical loss from early winter greater than 80%. Ozone loss was accompanied by activation of ClO, associated depletion of its reservoir ClONO2, and significant denitrification, which further delayed the recovery of ozone in spring. Once the PSC season halted, ClO was reconverted primarily into ClONO2. Compared to MIPAS observed 2003–2010 Arctic average values

  5. Semiconductor Sensors Application for Definition of Factor of Ozone Heterogeneous Destruction on Teflon Surface

    Directory of Open Access Journals (Sweden)

    Nataliya V. Finogenova

    2003-12-01

    Full Text Available In our paper we present the results of our research, which was carried out by means of semiconductor sensor techniques (SCS, which allowed evaluating heterogeneous death-rate of ozone (γ Teflon surface. When ozone concentration is near to Ambient Air Standard value, γ is assessed to be equal to 6,57*10-7. High technique response provide possibility to determine ozone contents in the air media and the percentage of ozone, decomposed on the communication surfaces and on the surfaces of installation in the low concentration range (1–100 ppb.

  6. Surface ozone in China: present-day distribution and long-term changes

    Science.gov (United States)

    Xu, X.; Lin, W.; Xu, W.

    2017-12-01

    Reliable knowledge of spatio-temporal variations of surface ozone is highly needed to assess the impacts of ozone on human health, ecosystem and climate. Although regional distributions and trends of surface ozone in European and North American countries have been well characterized, little is known about the variability of surface ozone in many other countries, including China, where emissions of ozone precursors have been changing rapidly in recent decades. Here we present the first comprehensive description of present-day (2013-2017) distribution and long-term changes of surface ozone in mainland China. Recent ozone measurements from China's air quality monitoring network (AQMN) are analyzed to show present-day distributions of a few ozone exposure metrics for urban environment. Long-term measurements of ozone at six background sites, a rural site and an urban are used to study the trends of ozone in background, rural and urban air, respectively. The average levels of ozone at the AQMN sites (mainly urban) are close to those found at many European and North American sites. However, ozone at most of the sites shows very large diurnal and seasonal variations so that ozone nonattainment can occur in many cities, particularly those in the North China Plain (NCP), the south of Northeast China (NEC), the Yangtze River Delta (YRD), the Pearl River Delta (PRD), and the Sichuan Basin-Chongqing region (SCB). In all these regions, particularly in the NCP, the maximum daily 8-h average (MDA8) ozone concentration can significantly exceed the national limit (75 ppb). High annual sum of ozone means over 35 ppb (SOMO35) exist mainly in the NCP, NEC and YRD, with regional averages over 4000 ppb·d. Surface ozone has significantly increased at Waliguan (a baseline site in western China) and Shangdianzi (a background site in the NCP), and decreased in winter and spring at Longfengshan (a background site in Northeast China). No clear trend can be derived from long-term measurements

  7. The role of Br2 and BrCl in surface ozone destruction at polar sunrise.

    Science.gov (United States)

    Foster, K L; Plastridge, R A; Bottenheim, J W; Shepson, P B; Finlayson-Pitts, B J; Spicer, C W

    2001-01-19

    Bromine atoms are believed to play a central role in the depletion of surface-level ozone in the Arctic at polar sunrise. Br2, BrCl, and HOBr have been hypothesized as bromine atom precursors, and there is evidence for chlorine atom precursors as well, but these species have not been measured directly. We report here measurements of Br2, BrCl, and Cl2 made using atmospheric pressure chemical ionization-mass spectrometry at Alert, Nunavut, Canada. In addition to Br2 at mixing ratios up to approximately 25 parts per trillion, BrCl was found at levels as high as approximately 35 parts per trillion. Molecular chlorine was not observed, implying that BrCl is the dominant source of chlorine atoms during polar sunrise, consistent with recent modeling studies. Similar formation of bromine compounds and tropospheric ozone destruction may also occur at mid-latitudes but may not be as apparent owing to more efficient mixing in the boundary layer.

  8. Impact of East Asian Summer Monsoon on Surface Ozone Pattern in China

    Science.gov (United States)

    Li, Shu; Wang, Tijian; Huang, Xing; Pu, Xi; Li, Mengmeng; Chen, Pulong; Yang, Xiu-Qun; Wang, Minghuai

    2018-01-01

    Tropospheric ozone plays a key role in regional and global atmospheric and climate systems. In East Asia, ozone can be affected both in concentration level and spatial pattern by typical monsoon climate. This paper uses three different indices to identify the strength of East Asian summer monsoon (EASM) and explores the possible impact of EASM intensity on the ozone pattern through synthetic and process analysis. The difference in ozone between three strong and three weak monsoon years was analyzed using the simulations from regional climate model RegCM4-Chem. It was found that EASM intensity can significantly influence the spatial distribution of ozone in the lower troposphere. When EASM is strong, ozone in the eastern part of China (28°N - 42° N) is reduced, but the inverse is detected in the north and south. The surface ozone difference ranges from -7 to 7 ppbv during the 3 months (June to August) of the EASM, with the most obvious difference in August. Difference of the 3 months' average ozone ranges from -3.5 to 4 ppbv. Process analysis shows that the uppermost factor controlling ozone level during summer monsoon seasons is the chemistry process. Interannual variability of EASM can impact the spatial distribution of ozone through wind in the lower troposphere, cloud cover, and downward shortwave radiation, which affect the transport and chemical formation of ozone. The phenomenon should be addressed when considering the interaction between ozone and the climate in East Asia region.

  9. Substituting HCFC-22 for HFC-410A: an environmental impact trade-off between the ozone depletion and climate change regimes

    Science.gov (United States)

    Wang, Z.; Fang, X.; Zhang, J.

    2015-12-01

    After the phase-out of hydrochlorofluorocarbons (HCFCs) as ozone-depleting substances pursuant to the requirements of the Montreal Protocol, hydrofluorocarbons (HFCs) are worldwide used as substitutes although the bulk of them are potent greenhouse gases (GHGs). Therefore, the alternation may bring side effect on global climate change. The trade-off of its environmental impacts between the ozone depletion and climate change regimes necessitates a quantification of the past and future consumption and emissions of both the original HCFCs and their alternative HFCs. Now a dilemma arise in China's RAC industry that HCFC-22, which has an ozone-depleting potential (ODP) of 0.055, has been replaced by HFC-410A, which is a blended potent GHG from respective 50% HFC-32 and HFC-125 with a global warming potential (GWP) of 1923.5. Here, we present our results of estimates of consumption and emissions of HCFC-22 and HFC-410A from 1994 to 2050. Historic emissions of HCFC-22 contributed to global total HCFCs by 4.0% (3.0%-5.6%) ODP-weighted. Projection under a baseline scenario shows future accumulative emissions of HFC-410A make up 5.9%-11.0% of global GWP-weighted HFCs emissions, and its annual contribution to national overall CO2 emissions can be 5.5% in 2050. This makes HCFC-22 and HFC-410A emissions of significant importance in ozone depletion and climate change regimes. Two mitigation scenarios were set to assess the mitigation performance under the North America Proposal and an accelerated schedule. In practice of international environmental agreement, "alternative to alternative" should be developed to avoid regrettable alternations.

  10. Impacts of Climate Change on Surface Ozone and Intercontinental Ozone Pollution: A Multi-Model Study

    Science.gov (United States)

    Doherty, R. M.; Wild, O.; Shindell, D. T.; Zeng, G.; MacKenzie, I. A.; Collins, W. J.; Fiore, A. M.; Stevenson, D. S.; Dentener, F. J.; Schultz, M. G.; hide

    2013-01-01

    The impact of climate change between 2000 and 2095 SRES A2 climates on surface ozone (O)3 and on O3 source-receptor (S-R) relationships is quantified using three coupled climate-chemistry models (CCMs). The CCMs exhibit considerable variability in the spatial extent and location of surface O3 increases that occur within parts of high NOx emission source regions (up to 6 ppbv in the annual average and up to 14 ppbv in the season of maximum O3). In these source regions, all three CCMs show a positive relationship between surface O3 change and temperature change. Sensitivity simulations show that a combination of three individual chemical processes-(i) enhanced PAN decomposition, (ii) higher water vapor concentrations, and (iii) enhanced isoprene emission-largely reproduces the global spatial pattern of annual-mean surface O3 response due to climate change (R2 = 0.52). Changes in climate are found to exert a stronger control on the annual-mean surface O3 response through changes in climate-sensitive O3 chemistry than through changes in transport as evaluated from idealized CO-like tracer concentrations. All three CCMs exhibit a similar spatial pattern of annual-mean surface O3 change to 20% regional O3 precursor emission reductions under future climate compared to the same emission reductions applied under present-day climate. The surface O3 response to emission reductions is larger over the source region and smaller downwind in the future than under present-day conditions. All three CCMs show areas within Europe where regional emission reductions larger than 20% are required to compensate climate change impacts on annual-mean surface O3.

  11. Chemical analysis and surface morphology of enamel following ozone application with different concentrations and exposure times

    Directory of Open Access Journals (Sweden)

    Iman I. Elsayad

    2011-04-01

    Full Text Available This study aimed to determine the effect of different ozone concentrations applied with different exposure times on the chemical composition and the surface morphology of enamel. Twenty human mandibular molars were divided into four groups according to ozone concentration and exposure times. Group A received 90 μg of ozone/ml oxygen for 1 min, group B received 90 μg of ozone/ml oxygen for 2 min, group C received 120 μg of ozone/ml oxygen for 1 min and group D received 120 μg of ozone/ml oxygen for 2 min. The ozone source was from a medical ozone generator equipped with a device to adjust the concentration. Buccal surfaces of teeth were tested before and after ozone application so that each tooth served as a control for itself, using Environmental Scanning Electron Microscope (ESEM connected to an Electron Dispersive Analytical X-ray (EDAX. Changes in calcium and phosphorus percentage levels were recorded and the Ca/P ratio was calculated. The values were statistically analyzed using the one-way ANOVA test with a level of significance set at P ⩽ 0.05. No statistical significant difference was found between the control and the tested groups in minerals content or ratio as P > 0.05. ESEM images showed enamel surface roughness with 2 min ozone exposure times. High ozone concentration with prolonged exposure time does not change the chemical composition of enamel. Applying ozone for 2 min alters the surface morphology of enamel causing variable degrees of roughness. Using high ozone concentrations with prolonged exposure times for caries reversal or prevention and for bleaching may be contraindicated if this changes the surface morphology of enamel.

  12. Surface modification of carbon nanohorns by helium plasma and ozone treatments

    Science.gov (United States)

    Lin, Zaw; Iijima, Toru; Selvam Karthik, Paneer; Yoshida, Mitsunobu; Hada, Masaki; Nishikawa, Takeshi; Hayashi, Yasuhiko

    2017-01-01

    In this paper, we describe the effects of helium plasma and ozone treatments on the dispersibility of carbon nanohorns (CNHs) in water. The experimental setups have been designed to efficiently generate helium plasma and ozone by dielectric barrier discharge at atmospheric pressure. After being treated with ozone, the oxygen-containing functional groups were introduced to the surface of CNHs, and are responsible for better dispersion. Helium plasma treatment was performed separately and it resulted in hydroxyl functional groups on the surface of CNHs. It was also found that the sizes of CNHs in water were smaller after ozone treatment. However, plasma-treated CNHs were bigger than ozone treated CNHs. The dispersed CNHs modified by ozone treatment were stable for more than three months without precipitation. In contrast, though helium plasma treatment introduced hydroxyl groups to the surface of CNHs, the dispersibility decreased and the flocculation of CNHs was observed in a few minutes.

  13. Basic Ozone Layer Science

    Science.gov (United States)

    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.

  14. Analysis of the Impact of Wildfire on Surface Ozone Record in the Colorado Front Range

    Science.gov (United States)

    McClure-Begley, A.; Petropavlovskikh, I. V.; Oltmans, S. J.; Pierce, R. B.; Sullivan, J. T.; Reddy, P. J.

    2015-12-01

    Ozone plays an important role on the oxidation capacity of the atmosphere, and at ground-level has negative impacts on human health and ecosystem processes. In order to understand the dynamics and variability of surface ozone, it is imperative to analyze individual sources, interactions between sources, transport, and chemical processes of ozone production and accumulation. Biomass burning and wildfires have been known to emit a suite of particulate matter and gaseous compounds into the atmosphere. These compounds, such as, volatile organic compounds, carbon monoxide, and nitrogen oxides are precursor species which aid in the photochemical production and destruction of ozone. The Colorado Front Range (CFR) is a region of complex interactions between pollutant sources and meteorological conditions which result in the accumulation of ozone. High ozone events in the CFR associated with fires are analyzed for 2003-2014 to develop understanding of the large scale influence and variability of ozone and wildfire relationships. This study provides analysis of the frequency of enhanced ozone episodes that can be confirmed to be transported within and affected by the fires and smoke plumes. Long-term records of surface ozone data from the CFR provide information on the impact of wildfire pollutants on seasonal and diurnal ozone behavior. Years with increased local fire activity, as well as years with increased long-range transport of smoke plumes, are evaluated for the effect on the long-term record and high ozone frequency of each location. Meteorological data, MODIS Fire detection images, NOAA HYSPLIT Back Trajectory analysis, NOAA Smoke verification model, Fire Tracer Data (K+), RAQMS Model, Carbon Monoxide data, and Aerosol optical depth retrievals are used with NOAA Global Monitoring Division surface ozone data from three sites in Colorado. This allows for investigation of the interactions between pollutants and meteorology which result in high surface ozone levels.

  15. Influence of baseline ozone on surface air quality in the western U.S

    Science.gov (United States)

    Jaffe, D. A.; Downey, N.

    2011-12-01

    As the ozone air quality standard is made more stringent, cities, counties and states will need a better understanding of the sources of ozone. While Eulerian models can provide important indications of the sources, they are often challenged by episodic emissions (eg wildfires), interannual variability and/or coarse model resolution. These challenges are especially problematic in the western United States. Thus we need improved tools to directly use available observations to better understand and identify ozone sources. In this study we examine the relationship between measured free tropospheric/baseline ozone and surface ozone at several receptor sites in the western U.S. Our focus is on air quality sites in the Pacific Northwest and Rocky Mtn region that exceed current or new air quality standards that have been proposed. Elevated sites in the Rocky Mtns are exposed to high ozone from the free troposphere. Significant interannual variations occur in spring, due to variations in baseline ozone, and in summer, due to variations in wildfires. In the Rocky Mtn region there are significant correlations between the surface and free tropospheric mixing ratios using both daily and monthly means for spring and summer months (see Jaffe 2011; DOI: 10.1021/es1028102). This implies that free tropospheric ozone mixes down and frequently contributes to elevated ozone at the surface. In the Pacific Northwest, we are using data from suburban and rural monitoring locations to identify ozone from local and non-local sources. The approach for both the Rocky Mtn and Pacific Northwest sites is to develop a statistical model for ozone using all available observations, (e.g. PM, meteorology, satellite data and trajectories) to quantify the variable contribution from baseline ozone. The statistical model can then be evaluated against actual observations of baseline ozone. The statistical model can also be useful to help identify "exceptional events" as defined by the US EPA.

  16. Changes in air quality and tropospheric composition due to depletion of stratospheric ozone and interactions with changing climate: implications for human and environmental health.

    Science.gov (United States)

    Madronich, S; Shao, M; Wilson, S R; Solomon, K R; Longstreth, J D; Tang, X Y

    2015-01-01

    local scale, ˙OH radicals respond rapidly to changes in UV radiation. However, on large (global) scales, models differ in their predictions by nearly a factor of two, with consequent uncertainties for estimating the atmospheric lifetime and concentrations of key greenhouse gases and air pollutants. Projections of future climate need to consider these uncertainties. No new negative environmental effects of substitutes for ozone depleting substances or their breakdown-products have been identified. However, some substitutes for the ozone depleting substances will continue to contribute to global climate change if concentrations rise above current levels.

  17. Evidence for midwinter chemical ozone destruction over Antartica

    Energy Technology Data Exchange (ETDEWEB)

    Voemel, H. [Univ. of Colorado, Boulder, CO (United States); Hoffmann, D.J.; Oltmans, S.J.; Harris, J.M. [NOAA Climate Monitoring and Diagnostics Laboratory, Boulder, CO (United States)

    1995-09-01

    Two ozone profiles on June 15 and June 19, obtained over McMurdo, Antartica, showed a strong depletion in stratospheric ozone, and a simultaneous profile of water vapor on June 19 showed the first clear signs of dehydration. The observation of Polar Stratospheric Clouds (PSCs) beginning with the first sounding showing ozone depletion, the indication of rehydration layers, which could be a sign for recent dehydration, and trajectory calculations indicate that the observed low ozone was not the result of transport from lower latitudes. during this time the vortex was strongly distorted, transporting PSC processed air well into sunlit latitudes where photochemical ozone destruction may have occurred. The correlation of ozone depletion and dehydration indicates that water ice PSCs provided the dominant surface for chlorine activation. An analysis of the time when the observed air masses could have formed type II PSCs for the first time limits the time scale for the observed ozone destruction to about 4 days.

  18. Variations of surface ozone concentration across the Klang Valley, Malaysia

    Science.gov (United States)

    Latif, Mohd Talib; Huey, Lim Shun; Juneng, Liew

    2012-12-01

    Hourly air quality data covering the period 2004-2008 was obtained from the Air Quality Division, the Department of Environment (DOE) through long-term monitoring by Alam Sekitar Sdn. Bhd. (ASMA) were analysed to investigate the variations of surface ozone (O3) in the Klang Valley, Malaysia. A total of nine monitoring stations were selected for analysis in this study and the results show that there are distinct seasonal patterns in the surface O3 across the Klang Valley. A high surface O3 concentration is usually observed between January and April, while a low surface O3 concentration is found between June and August. Analysis of daily variations in surface O3 and the precursors - NO, NO2, CO, NMHC and UVb, indicate that the surface O3 photochemistry in this study area exhibits a positive response to the intensity and wavelength in UVb while being influenced by the concentration of NOx, particularly through tritration processes. Although results from our study suggested that NMHCs may influence the maximum O3 concentration, further investigation is required. Wind direction during different monsoons was found to influence the concentration of O3 around the Klang Valley. HYSPLIT back trajectories (-72 h) were used to indicate the air-mass transport patterns on days with high concentrations of surface O3 in the study area. Results show that 47% of the high O3 days was associated with the localized circulation. The remaining 32% and 22% were associated with mid-range and long-range transport across the South China Sea from the northeast.

  19. Ozone-surface interactions: Investigations of mechanisms, kinetics, mass transport, and implications for indoor air quality

    Energy Technology Data Exchange (ETDEWEB)

    Morrison, Glenn Charles [Univ. of California, Berkeley, CA (United States)

    1999-12-01

    In this dissertation, results are presented of laboratory investigations and mathematical modeling efforts designed to better understand the interactions of ozone with surfaces. In the laboratory, carpet and duct materials were exposed to ozone and measured ozone uptake kinetics and the ozone induced emissions of volatile organic compounds. To understand the results of the experiments, mathematical methods were developed to describe dynamic indoor aldehyde concentrations, mass transport of reactive species to smooth surfaces, the equivalent reaction probability of whole carpet due to the surface reactivity of fibers and carpet backing, and ozone aging of surfaces. Carpets, separated carpet fibers, and separated carpet backing all tended to release aldehydes when exposed to ozone. Secondary emissions were mostly n-nonanal and several other smaller aldehydes. The pattern of emissions suggested that vegetable oils may be precursors for these oxidized emissions. Several possible precursors and experiments in which linseed and tung oils were tested for their secondary emission potential were discussed. Dynamic emission rates of 2-nonenal from a residential carpet may indicate that intermediate species in the oxidation of conjugated olefins can significantly delay aldehyde emissions and act as reservoir for these compounds. The ozone induced emission rate of 2-nonenal, a very odorous compound, can result in odorous indoor concentrations for several years. Surface ozone reactivity is a key parameter in determining the flux of ozone to a surface, is parameterized by the reaction probability, which is simply the probability that an ozone molecule will be irreversibly consumed when it strikes a surface. In laboratory studies of two residential and two commercial carpets, the ozone reaction probability for carpet fibers, carpet backing and the equivalent reaction probability for whole carpet were determined. Typically reaction probability values for these materials were 10

  20. Global Model Comparison with NOAA Observed Surface Ozone to Understand Transport in the Arctic

    Science.gov (United States)

    Petropavlovskikh, I. V.; McClure-Begley, A.; Tummon, F.; Tilmes, S.; Yudina, A.; Crepinsek, S.; Uttal, T.

    2016-12-01

    The Arctic region is rapidly gaining interest and support for scientific studies to help understand and characterize the processes, sources, and chemical composition of the Arctic environment. In order to understand the Arctic climate system and the changes that are occurring, it is imperative to know the behavior and impact of atmospheric constituents. As a secondary pollutant which impacts the oxidation capacity and radiative forcing of the atmosphere, ozone is an imperative species to characterize. Global atmospheric models help to confirm and understand the influence of long-distance transport on local ozone conditions. This analysis highlights the winter season when ozone conditions are not being driven by photochemical influence, and transport is the prevalent means of ozone variation. In order to ensure adequate representation of ozone conditions and source regions, model comparison verifies the ability of models to represent the behavior of ozone at the surface. Ozone mixing ratios observed from Barrow, Alaska and Summit, Greenland, are critical observations to provide fundamental knowledge of the behavior and trends of ground-level ozone in the Arctic. The observed surface ozone and wind data are compared against two different global climate-chemistry models to assess the ability for models to simulate surface ozone in the arctic region. The CCM SOCOL (Modeling tools for studies of Solar Climate Ozone Links) and Community Earth System Model (CESM1) CAM4-chem are compared to observational measurements. Comparisons between the model and observations are used as the first step in understanding of the long-range transport contribution to ozone variability in the boundary layer of the Arctic environment. An improvement in agreement between observations and chemistry-climate hind cast is found when the model is forced with reanalysis wind conditions.

  1. Depletion of stratospheric ozone over the Antarctic and Arctic: Responses of plants of polar terrestrial ecosystems to enhanced UV-B, an overview

    International Nuclear Information System (INIS)

    Rozema, Jelte; Boelen, Peter; Blokker, Peter

    2005-01-01

    Depletion of stratospheric ozone over the Antarctic has been re-occurring yearly since 1974, leading to enhanced UV-B radiation. Arctic ozone depletion has been observed since 1990. Ozone recovery has been predicted by 2050, but no signs of recovery occur. Here we review responses of polar plants to experimentally varied UV-B through supplementation or exclusion. In supplementation studies comparing ambient and above ambient UV-B, no effect on growth occurred. UV-B-induced DNA damage, as measured in polar bryophytes, is repaired overnight by photoreactivation. With UV exclusion, growth at near ambient may be less than at below ambient UV-B levels, which relates to the UV response curve of polar plants. UV-B screening foils also alter PAR, humidity, and temperature and interactions of UV with environmental factors may occur. Plant phenolics induced by solar UV-B, as in pollen, spores and lignin, may serve as a climate proxy for past UV. Since the Antarctic and Arctic terrestrial ecosystems differ essentially (e.g. higher species diversity and more trophic interactions in the Arctic), generalization of polar plant responses to UV-B needs caution. - Polar plant responses to UV-B may be different in the Arctic than Antarctic regions

  2. Depletion of stratospheric ozone over the Antarctic and Arctic: Responses of plants of polar terrestrial ecosystems to enhanced UV-B, an overview

    Energy Technology Data Exchange (ETDEWEB)

    Rozema, Jelte [Department of Systems Ecology, Institute of Ecological Science, Climate Centre, Vrije Universiteit, De Boelelaan 1087, 1081 HV Amsterdam (Netherlands)]. E-mail: jelte.rozema@ecology.falw.vu.nl; Boelen, Peter [Department of Systems Ecology, Institute of Ecological Science, Climate Centre, Vrije Universiteit, De Boelelaan 1087, 1081 HV Amsterdam (Netherlands); Blokker, Peter [Department of Systems Ecology, Institute of Ecological Science, Climate Centre, Vrije Universiteit, De Boelelaan 1087, 1081 HV Amsterdam (Netherlands)

    2005-10-15

    Depletion of stratospheric ozone over the Antarctic has been re-occurring yearly since 1974, leading to enhanced UV-B radiation. Arctic ozone depletion has been observed since 1990. Ozone recovery has been predicted by 2050, but no signs of recovery occur. Here we review responses of polar plants to experimentally varied UV-B through supplementation or exclusion. In supplementation studies comparing ambient and above ambient UV-B, no effect on growth occurred. UV-B-induced DNA damage, as measured in polar bryophytes, is repaired overnight by photoreactivation. With UV exclusion, growth at near ambient may be less than at below ambient UV-B levels, which relates to the UV response curve of polar plants. UV-B screening foils also alter PAR, humidity, and temperature and interactions of UV with environmental factors may occur. Plant phenolics induced by solar UV-B, as in pollen, spores and lignin, may serve as a climate proxy for past UV. Since the Antarctic and Arctic terrestrial ecosystems differ essentially (e.g. higher species diversity and more trophic interactions in the Arctic), generalization of polar plant responses to UV-B needs caution. - Polar plant responses to UV-B may be different in the Arctic than Antarctic regions.

  3. Ozone decay on stainless steel and sugarcane bagasse surfaces

    Science.gov (United States)

    Souza-Corrêa, Jorge A.; Oliveira, Carlos; Amorim, Jayr

    2013-07-01

    Ozone was generated using dielectric barrier discharges at atmospheric pressure to treat sugarcane bagasse for bioethanol production. It was shown that interaction of ozone molecules with the pretreatment reactor wall (stainless steel) needs to be considered during bagasse oxidation in order to evaluate the pretreatment efficiency. The decomposition coefficients for ozone on both materials were determined to be (3.3 ± 0.2) × 10-8 for stainless steel and (2.0 ± 0.3) × 10-7 for bagasse. The results have indicated that ozone decomposition has occurred more efficiently on the biomass material.

  4. Global impacts of surface ozone changes on crop yields and land use

    NARCIS (Netherlands)

    Chuwah, Clifford; van Noije, Twan; van Vuuren, Detlef P.|info:eu-repo/dai/nl/11522016X; Stehfest, Elke; Hazeleger, Wilco

    2015-01-01

    Exposure to surface ozone has detrimental impacts on vegetation and crop yields. In this study, we estimate ozone impacts on crop production and subsequent impacts on land use in the 2005-2050 period using results of the TM5 atmospheric chemistry and IMAGE integrated assessment model. For the crops

  5. Global impacts of surface ozone changes on crop yields and land use

    NARCIS (Netherlands)

    Chuwah, C.D.; Noije, van Twan; Vuuren, van Detlef P.; Stehfest, Elke; Hazeleger, Wilco

    2015-01-01

    Exposure to surface ozone has detrimental impacts on vegetation and crop yields. In this study, we estimate ozone impacts on crop production and subsequent impacts on land use in the 2005-2050 period using results of the TM5 atmospheric chemistry and IMAGE integrated assessment model. For the

  6. Ozonation of benzothiazole saturated-activated carbons: Influence of carbon chemical surface properties

    International Nuclear Information System (INIS)

    Valdes, H.; Zaror, C.A.

    2006-01-01

    The combined or sequential use of ozone and activated carbon to treat toxic effluents has increased in recent years. However, little is known about the influence of carbon surface active sites on ozonation of organic adsorbed pollutants. This paper presents experimental results on the effect of metal oxides and oxygenated surface groups on gaseous ozonation of spent activated carbons. Benzothiazole (BT) was selected as a target organic compound in this study due to its environmental concern. Activated carbons with different chemical surface composition were prepared from a Filtrasorb-400 activated carbon. Pre-treatment included: ozonation, demineralisation, and deoxygenation of activated carbon. Ozonation experiments of BT saturated-activated carbons were conducted in a fixed bed reactor loaded with 2 g of carbon samples. The reactor was fed with an O 2 /O 3 gas mixture (2 dm 3 /min, 5 g O 3 /h), for a given exposure time, in the range 10-120 min, at 298 K and 1 atm. Results show that extended gaseous ozonation of activated carbon saturated with BT led to the effective destruction of the adsorbate by oxidation reactions. Oxidation of BT adsorbed on activated carbon seemed to occur via both direct reaction with ozone molecules, and by oxygen radical species generated by catalytic ozone decomposition on metallic surface sites

  7. Chromium depletion on the surface of nickel based alloys

    International Nuclear Information System (INIS)

    Dille, E.R.; McDonald, J.L.; Berry, P.

    1988-01-01

    Successful selection of corrosion resistant materials for flue gas desuflurization applications is tricky business at best. Most simulated, accelerated, concentrated corrosion tests try to rank materials to known corrosive condition. If you check the actual data, occasionally you find anomalies such as highly corrosion resistant materials performing below what was expected, while the rest of the group is performing normally. In the field the authors have observed similar results with few acceptable explanations. Recently the authors have found numerous cases of Ni/Cr/Mo alloys with a surface analysis below the ASTM specified range for the element chromium. These surface analysis have been done with a portable X-ray Fluorescent Instrument with the initial results confirmed by an independent laboratory

  8. Influences of the boundary layer evolution on surface ozone ...

    Indian Academy of Sciences (India)

    (1998) showed that the change in tropical ozone is highly sensitive to climate forcing in the tropics. Considering the importance of tropical tropo- sphere, attempts have been made for the measure- ment of ozone and precursors along with meteoro- logical parameters over the Indian region in which the roles of chemistry and ...

  9. Influences of the boundary layer evolution on surface ozone ...

    Indian Academy of Sciences (India)

    Considering the importance of tropical tropo- sphere, attempts have been made for the measure- ment of ozone and precursors along with meteoro- logical parameters over the Indian region in which the roles of chemistry and meteorology in control- ling the ozone levels have been examined over this region (e.g., Naja and ...

  10. Influences of the boundary layer evolution on surface ozone ...

    Indian Academy of Sciences (India)

    2016-08-26

    Aug 26, 2016 ... A chemical box model simulation indicates about 17% reduction in the daytime ozone levels during the conditions of suppressed PBL in comparison with those of higher PBL conditions. On a few occasions, substantially elevated ozone levels (as high as 90 ppbv) were observed during late evening hours, ...

  11. Impact of increased ultraviolet-B radiation stress due to stratospheric ozone depletion on N2 fixation in traditional African commercial legumes

    International Nuclear Information System (INIS)

    Chimphango, S.B.M.; Musil, C.F.; Dakora, F.D.

    2004-01-01

    Reports of diminished nodule formation and nitroge-nase activity in some Asian tropical legumes exposed to above-ambient levels of ultraviolet-B (UV-B: 280-315nm) radiation have raised concerns as to the impact of stratospheric ozone depletion on generally poorly developed traditional African farming systems confronted by the high cost and limited availability of chemical fertilisers. These rely on N 2 -fixing legumes as the cheapest source of N for maintaining soil fertility and sustainable yields in the intrinsically infertile and heterogeneous African soils. In view of this, we examined the effects of supplemental UV-B radiation approximating 15% and 25% depletions in the total ozone column on N 2 fixation in eight traditional African commercial legume species representing crop, forest, medicinal, ornamental and pasture categories. In all categories examined, except medicinal, supplemental UV-B had no effect on root non-structural carbohydrates, antho-cyanins and flavonoids, known to signal Rhizobiaceae micro-symbionts and promote nodule formation, or on nodule mass, activity and quantities of N fixed in different plant organs and whole plants. In contrast, in the medicinal category Cyclopia maculata (Honeybush) a slow growing commercially important herbal beverage with naturally high flavonoid concentrations, displayed decreased nodule activity and quantities of N fixed in different plant organs and whole plants with increased UV-B. This study's findings conclude negligible impacts of ozone depletion on nitrogen fixation and soil fertility in most traditional African farming systems, these limited to occasional inhibition of nodule induction in some crops. (author)

  12. Investigation of ozone zero phenomenon using new electrode and surface analysis technique

    Science.gov (United States)

    Taguchi, M.; Ochiai, Y.; Kawagoe, R.; Kato, Y.; Teranishi, K.; Suzuki, S.; Itoh, H.

    2011-07-01

    Results of our experimental investigation on the ozone zero phenomenon suggested us the importance of the electrode surface condition. This means that the main cause of the phenomenon, that is, temporal decrease of ozone concentration at the outlet of DBD type ozone generator and the recovery characteristics from the phenomenon are considered as the surface reaction process, which are influenced strongly by the surface condition. The surface condition is never constant during the ozone generation and varies gradually or remarkably with time depending on the experimental conditions. Therefore we have been continued to make clear the cause of the phenomenon, for example, the reproducibility of the phenomenon, using new electrodes and together with the surface analysis technique etc. In this paper, we describe on the above results and discussion.

  13. Ultraviolet light depletes surface markers of Langerhans cells

    International Nuclear Information System (INIS)

    Aberer, W.; Schuler, G.; Stingl, G.; Hoenigsmann, H.; Wolff, K.

    1981-01-01

    This report defines the influence of ultraviolet light (UV) on Langerhans cells (LC). Human volunteers and hairless mice (Swiss ha/ha) were exposed to various single and/or cumulative doses of either UV-A, UV-B, or UV-A plus small amounts of UV-B (UV-A (+B)). 24 hr after the last irradiation, morphology of the entire epidermis was evaluated by both light and electron microscopy while LC, in addition, were tested for expression of specific histochemical (ATPase) and functional immunological markers (Ia antigens). In both men and mice, cumulative doses of either 80-120 J/cm2 UV-A (+B) or 1-2 X 100 J/cm2 UV-A resulted in a dramatic reduction of cells exhibiting ATPase and Ia-reactivity. In the UV-B spectrum, single doses of 60-80 mJ/cm2 produced a virtually complete elimination of LC membrane markers. By contrast, pemphigus antigens of keratinocytes were unaffected by these energy doses. Electron microscopy revealed cellular damage of some LC after UV-doses which produce a virtually complete abolition of LC membrane markers. At certain dose ranges (15-30 mJ/cm2 UV-B and 1 x 40 to 2 x 100 J/cm2 UV-A) LC were the only epidermal cells to display morphological damage at the ultrastructural level whereas higher doses affected all epidermal cells. The finding that LC surface markers and to a lesser extent the cells themselves are particularly susceptible to UV irradiation has important implications in view of previous findings that LC are potent stimulators of antigen-specific and allogeneic T cell activation. UV-induced alteration of LC plasma membrane integrity may represent a tool to manipulate adverse immune reactions involving the epidermis

  14. Ozone time scale decomposition and trend assessment from surface observations

    Science.gov (United States)

    Boleti, Eirini; Hueglin, Christoph; Takahama, Satoshi

    2017-04-01

    Emissions of ozone precursors have been regulated in Europe since around 1990 with control measures primarily targeting to industries and traffic. In order to understand how these measures have affected air quality, it is now important to investigate concentrations of tropospheric ozone in different types of environments, based on their NOx burden, and in different geographic regions. In this study, we analyze high quality data sets for Switzerland (NABEL network) and whole Europe (AirBase) for the last 25 years to calculate long-term trends of ozone concentrations. A sophisticated time scale decomposition method, called the Ensemble Empirical Mode Decomposition (EEMD) (Huang,1998;Wu,2009), is used for decomposition of the different time scales of the variation of ozone, namely the long-term trend, seasonal and short-term variability. This allows subtraction of the seasonal pattern of ozone from the observations and estimation of long-term changes of ozone concentrations with lower uncertainty ranges compared to typical methodologies used. We observe that, despite the implementation of regulations, for most of the measurement sites ozone daily mean values have been increasing until around mid-2000s. Afterwards, we observe a decline or a leveling off in the concentrations; certainly a late effect of limitations in ozone precursor emissions. On the other hand, the peak ozone concentrations have been decreasing for almost all regions. The evolution in the trend exhibits some differences between the different types of measurement. In addition, ozone is known to be strongly affected by meteorology. In the applied approach, some of the meteorological effects are already captured by the seasonal signal and already removed in the de-seasonalized ozone time series. For adjustment of the influence of meteorology on the higher frequency ozone variation, a statistical approach based on Generalized Additive Models (GAM) (Hastie,1990;Wood,2006), which corrects for meteorological

  15. Surface Monitoring Data for PM2.5 and Ozone

    Data.gov (United States)

    Washington University St Louis — AIRNOW is an EPA program in collaboration with the States to gather and distribute hourly near-realtime data from several hundred continuous PM2.5 and ozone monitors.

  16. Climate Change Impacts on Projections of Excess Mortality at 2030 using Spatially-Varying Ozone-Temperature Risk Surfaces

    Science.gov (United States)

    Wilson, Ander; Reich, Brian J.; Nolte, Christopher G.; Spero, Tanya L.; Hubbell, Bryan; Rappold, Ana G.

    2017-01-01

    We project the change in ozone-related mortality burden attributable to changes in climate between a historical (1995–2005) and near-future (2025–2035) time period while incorporating a nonlinear and synergistic effect of ozone and temperature on mortality. We simulate air quality from climate projections varying only biogenic emissions and holding anthropogenic emissions constant, thus attributing changes in ozone only to changes in climate and independent of changes in air pollutant emissions. We estimate nonlinear, spatially-varying, ozone-temperature risk surfaces for 94 US urban areas using observed data. Using the risk surfaces and climate projections we estimate daily mortality attributable to ozone exceeding 40 ppb (moderate level) and 75 ppb (US ozone NAAQS) for each time period. The average increases in city-specific median April-October ozone and temperature between time periods are 1.02 ppb and 1.94°F; however, the results varied by region. Increases in ozone due to climate change result in an increase in ozone-mortality burden. Mortality attributed to ozone exceeding 40 ppb increases by 7.7% (1.6%, 14.2%). Mortality attributed to ozone exceeding 75 ppb increases by 14.2% (1.6%, 28.9%). The absolute increase in excess ozone mortality is larger for changes in moderate ozone levels, reflecting the larger number of days with moderate ozone levels. PMID:27005744

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

    Science.gov (United States)

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

    2013-05-01

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

  18. Plant responses to current solar ultraviolet-B radiation and to supplemented solar ultraviolet-B radiation simulating ozone depletion: an experimental comparison.

    Science.gov (United States)

    Rousseaux, M Cecilia; Flint, Stephan D; Searles, Peter S; Caldwell, Martyn M

    2004-01-01

    Field experiments assessing UV-B effects on plants have been conducted using two contrasting techniques: supplementation of solar UV-B with radiation from fluorescent UV lamps and the exclusion of solar UV-B with filters. We compared these two approaches by growing lettuce and oat simultaneously under three conditions: UV-B exclusion, near-ambient UV-B (control) and UV-B supplementation (simulating a 30% ozone depletion). This permitted computation of "solar UV-B" and "supplemental UV-B" effects. Microclimate and photosynthetically active radiation were the same under the two treatments and the control. Excluding UV-B changed total UV-B radiation more than did supplementing UV-B, but the UV-B supplementation contained more "biologically effective" shortwave radiation. For oat, solar UV-B had a greater effect than supplemental UV-B on main shoot leaf area and main shoot mass, but supplemental UV-B had a greater effect on leaf and tiller number and UV-B-absorbing compounds. For lettuce, growth and stomatal density generally responded similarly to both solar UV-B and supplemented UV-B radiation, but UV-absorbing compounds responded more to supplemental UV-B, as in oat. Because of the marked spectral differences between the techniques, experiments using UV-B exclusion are most suited to assessing effects of present-day UV-B radiation, whereas UV-B supplementation experiments are most appropriate for addressing the ozone depletion issue.

  19. Surface Ozone Variability and Trends over the South African Highveld from 1990 to 2007

    Science.gov (United States)

    Balashov, Nikolay V.; Thompson, Anne M.; Piketh, Stuart J.; Langerman, Kristy E.

    2014-01-01

    Surface ozone is a secondary air pollutant formed from reactions between nitrogen oxides (NOx = NO + NO2) and volatile organic compounds in the presence of sunlight. In this work we examine effects of the climate pattern known as the El Niño-Southern Oscillation (ENSO) and NOx variability on surface ozone from 1990 to 2007 over the South African Highveld, a heavily populated region in South Africa with numerous industrial facilities. Over summer and autumn (December-May) on the Highveld, El Niño, as signified by positive sea surface temperature (SST) anomalies over the central Pacific Ocean, is typically associated with drier and warmer than normal conditions favoring ozone formation. Conversely, La Niña, or negative SST anomalies over the central Pacific Ocean, is typically associated with cloudier and above normal rainfall conditions, hindering ozone production. We use a generalized regression model to identify any linear dependence that the Highveld ozone, measured at five air quality monitoring stations, may have on ENSO and NOx. Our results indicate that four out of the five stations exhibit a statistically significant sensitivity to ENSO at some point over the December-May period where El Niño amplifies ozone formation and La Niña reduces ozone formation. Three out of the five stations reveal statistically significant sensitivity to NOx variability, primarily in winter and spring. Accounting for ENSO and NOx effects throughout the study period of 18 years, two stations exhibit statistically significant negative ozone trends in spring, one station displays a statistically significant positive trend in August, and two stations show no statistically significant change in surface ozone.

  20. A laboratory study of the UV Absorption Spectrum of the ClO Dimer (Cl2O2) and the Implications for Polar Stratospheric Ozone Depletion

    Science.gov (United States)

    Papanastasiou, D. K.; Papadimitriou, V. C.; Fahey, D. W.; Burkholder, J. B.

    2009-12-01

    Chlorine containing species play an important role in catalytic ozone depleting cycles in the Antarctic and Arctic stratosphere. The ClO dimer (Cl2O2) catalytic ozone destruction cycle accounts for the majority of the observed polar ozone loss. A key step in this catalytic cycle is the UV photolysis of Cl2O2. The determination of the Cl2O2 UV absorption spectrum has been the subject of several studies since the late 1980’s. Recently, Pope et al. (J. Phys. Chem. A, 111, 4322, 2007) reported significantly lower absorption cross sections for Cl2O2 for the atmospherically relevant wavelength region, >300 nm, than currently recommended for use in atmospheric models. If correct, the Pope et al. results would alter our understanding of the chemistry of polar ozone depletion significantly. In this study, the UV absorption spectrum and absolute cross sections of gas-phase Cl2O2 are reported for the wavelength range 200 - 420 nm at ~200 K. Sequential pulsed laser photolysis of various precursors were used to produce the ClO radical and Cl2O2 via the subsequent ClO + ClO + M reaction under static conditions. UV absorption spectra of the reaction mixture were measured using a diode array spectrometer after completion of the gas-phase radical chemistry. The spectral analysis utilized the observed isosbestic points, reaction stoichiometry, and chlorine mass balance to determine the UV spectrum and absolute cross section of Cl2O2. A complementary experimental technique similar to that used by Pope et al. was also used in this study. We obtained consistent Cl2O2 UV absorption spectra using the two different techniques. The Cl2O2 absorption cross sections for wavelengths in the 300 - 420 nm range were found to be in very good agreement with the values reported previously by Burkholder et al. (J. Phys. Chem. A, 94, 687, 1990) and significantly greater than the Pope et al. values in this atmospherically important wavelength region. A possible explanation for the disagreement with

  1. Surface ozone exposures measured at clean locations around the world.

    Science.gov (United States)

    Lefohn, A S; Krupa, S V; Winstanley, D

    1990-01-01

    For assessing the effects of air pollution on vegetation, some researchers have used control chambers as the basis of comparison between crops and trees grown in contemporary polluted rural locations and those grown in a clean environment. There has been some concern whether the arbitrary ozone level of 0.025 ppm and below, often used in charcoal-filtration chambers to simulate the natural background concentration of ozone, is appropriate. Because of the many complex and man-made factors that influence ozone levels, it is difficult to determine natural background. To identify a range of ozone exposures that occur at 'clean' sites, we have calculated ozone exposures observed at a number of 'clean' monitoring sites located in the United States and Canada. We do not claim that these sites are totally free from human influence, but rather than the ozone concentrations observed at these 'clean' sites may be appropriate for use by vegetation researchers in control chambers as pragmatic and defensible surrogates for natural background. For comparison, we have also calculated ozone exposures observed at four 'clean' remote sites in the Northern and Southern Hemispheres and at two remote sites (Whiteface Mountain, NY and Hohenpeissenberg, FRG) that are considered to be more polluted. Exposure indices relevant for describing the relationship between ozone and vegetation effects were applied. For studying the effects of ozone on vegetation, the higher concentrations are of interest. The sigmoidally-weighted index appeared to best separate those sites that experienced frequent high concentration exposures from those that experienced few high concentrations. Although there was a consistent seasonal pattern for the National Oceanic and Atmospheric Administration (NOAA) Geophysical Monitoring for Climate Change (GMCC) sites indicating a winter/spring maximum, this was not the case for the other remote sites. Some sites in the continental United States and southern Canada

  2. Contribution of some ozone depleting substances (ODS) and greenhouse gases (GHGs) on total column ozone growth at Srinagar (34°N, 74.8°E), India

    Science.gov (United States)

    Jana, P. K.; Saha, D. K.; Sarkar, D.

    2013-02-01

    A critical analysis has been made on the contribution of CFC-11, CFC-12, CFC-113, CH3Cl, CH3Br, CCl4, CH3CCl3, HCFCs, halons, WMO (World Meteorological Organization) minor constituents, CH4, N2O and water vapour to the variation of total column ozone (TCO) concentration at the station in Srinagar (34°N, 74.8°E), India from 1992 to 2003. With the implementation of Montreal Protocol, though the concentrations of CFC-11, CFC-113, CH3Cl, CH3Br, CCl4 and CH3CCl3 had decreased, the concentrations of CFC-12, HCFCs, halons, WMO minor constituents, CH4, N2O and water vapour had increased, as a result of which TCO had risen from 1992 to 2003 at the above station. The nature of yearly variations of concentrations of the above ozone depleting substances and GHGs as well as ozone has been presented. Possible explanations for build-up of TCO have also been offered.

  3. Responses of surface ozone air quality to anthropogenic nitrogen deposition in the Northern Hemisphere

    Science.gov (United States)

    Zhao, Yuanhong; Zhang, Lin; Tai, Amos P. K.; Chen, Youfan; Pan, Yuepeng

    2017-08-01

    Human activities have substantially increased atmospheric deposition of reactive nitrogen to the Earth's surface, inducing unintentional effects on ecosystems with complex environmental and climate consequences. One consequence remaining unexplored is how surface air quality might respond to the enhanced nitrogen deposition through surface-atmosphere exchange. Here we combine a chemical transport model (GEOS-Chem) and a global land model (Community Land Model, CLM) to address this issue with a focus on ozone pollution in the Northern Hemisphere. We consider three processes that are important for surface ozone and can be perturbed by the addition of atmospheric deposited nitrogen - namely, emissions of biogenic volatile organic compounds (VOCs), ozone dry deposition, and soil nitrogen oxide (NOx) emissions. We find that present-day anthropogenic nitrogen deposition (65 Tg N a-1 to the land), through enhancing plant growth (represented as increases in vegetation leaf area index, LAI, in the model), could increase surface ozone from increased biogenic VOC emissions (e.g., a 6.6 Tg increase in isoprene emission), but it could also decrease ozone due to higher ozone dry deposition velocities (up to 0.02-0.04 cm s-1 increases). Meanwhile, deposited anthropogenic nitrogen to soil enhances soil NOx emissions. The overall effect on summer mean surface ozone concentrations shows general increases over the globe (up to 1.5-2.3 ppbv over the western US and South Asia), except for some regions with high anthropogenic NOx emissions (0.5-1.0 ppbv decreases over the eastern US, western Europe, and North China). We compare the surface ozone changes with those driven by the past 20-year climate and historical land use changes. We find that the impacts from anthropogenic nitrogen deposition can be comparable to the climate- and land-use-driven surface ozone changes at regional scales and partly offset the surface ozone reductions due to land use changes reported in previous studies

  4. Comment on "Cosmic-ray-driven reaction and greenhouse effect of halogenated molecules: Culprits for atmospheric ozone depletion and global climate change"

    Science.gov (United States)

    Müller, Rolf; Grooß, Jens-Uwe

    2014-04-01

    Lu's "cosmic-ray-driven electron-induced reaction (CRE) theory" is based on the assumption that the CRE reaction of halogenated molecules (e.g., chlorofluorocarbons (CFCs), HCl, ClONO2) adsorbed or trapped in polar stratospheric clouds in the winter polar stratosphere is the key step in forming photoactive halogen species that are the cause of the springtime ozone hole. This theory has been extended to a warming theory of halogenated molecules for climate change. In this comment, we discuss the chemical and physical foundations of these theories and the conclusions derived from the theories. First, it is unclear whether the loss rates of halogenated molecules induced by dissociative electron attachment (DEA) observed in the laboratory can also be interpreted as atmospheric loss rates, but even if this were the case, the impact of DEA-induced reactions on polar chlorine activation and ozone loss in the stratosphere is limited. Second, we falsify several conclusions that are reported on the basis of the CRE theory: There is no polar ozone loss in darkness, there is no apparent 11-year periodicity in polar total ozone measurements, the age of air in the polar lower stratosphere is much older than 1-2 years, and the reported detection of a pronounced recovery (by about 20-25%) in Antarctic total ozone measurements by the year 2010 is in error. There are also conclusions about the future development of sea ice and global sea level which are fundamentally flawed because Archimedes' principle is neglected. Many elements of the CRE theory are based solely on correlations between certain datasets which are no substitute for providing physical and chemical mechanisms causing a particular behavior noticeable in observations. In summary, the CRE theory cannot be considered as an independent, alternative mechanism for polar stratospheric ozone loss and the conclusions on recent and future surface temperature and global sea level change do not have a physical basis.

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

    Science.gov (United States)

    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

  6. Variability of surface ozone with cloud coverage over Kolkata, India

    Indian Academy of Sciences (India)

    3Department of Atmospheric Sciences, Calcutta University, 92, A.P.C. Road, Kolkata 700 009, India. ∗. Corresponding author. e-mail: .... 2004). Kolkata also experiences substan- tial level of pollution from automobiles (Mallik et al. ... from Ozone Monitoring Instrument (OMI) onboa rd the Aura satellite. This study employs the ...

  7. Surface ozone variation at Bhubaneswar and intra-corelationship ...

    Indian Academy of Sciences (India)

    transport of airmass from mainly Indo-Gangetic Plains (IGP) and western part of Indian peninsula, a major industrial hub. In other seasons, wind ... 1164. P S Mahapatra et al. processes. Downward transport of the ozone-rich ... izer and food processing industries along with ther- mal power plants have been set-up in the ...

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

    Science.gov (United States)

    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.; hide

    2016-01-01

    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 deg. x 0.3125 deg. 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 15 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

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

    Science.gov (United States)

    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

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

    Directory of Open Access Journals (Sweden)

    K. R. Travis

    2016-11-01

    Full Text Available 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

  11. Preliminary SEM Observations on the Surface of Elastomeric Impression Materials after Immersion or Ozone Disinfection

    Science.gov (United States)

    Prombonas, Anthony; Yannikakis, Stavros; Karampotsos, Thanasis; Katsarou, Martha-Spyridoula; Drakoulis, Nikolaos

    2016-01-01

    Introduction Surface integrity of dental elastomeric impression materials that are subjected to disinfection is of major importance for the quality of the final prosthetic restorations. Aim The aim of this qualitative Scanning Electronic Microscopy (SEM) study was to reveal the effects of immersion or ozone disinfection on the surface of four dental elastomeric impression materials. Materials and Methods Four dental elastomeric impression material brands were used (two vinyl polysiloxane silicones, one polyether, and one vinyl polyether silicone). Total of 32 specimens were fabricated, eight from each impression material. Specimens were immersion (0.525% sodium hypochlorite solution or 0.3% benzalkonium chloride solution) or ozone disinfected or served as controls and examined with SEM. Results Surface degradation was observed on several speci-mens disinfected with 0.525% sodium hypochlorite solution. Similar wavy-wrinkling surface structures were observed in almost all specimens, when treated either with 0.3% benzalkonium chloride solution or ozone. Conclusion The SEM images obtained from this study revealed that both immersion disinfectants and ozone show similar impression material surface alterations. Ozone seems to be non-inferior as compared to immersion disinfectants, but superior as to environmental protection. PMID:28208993

  12. First observations of surface ozone concentration from the summit region of Mount Everest

    Science.gov (United States)

    Semple, John L.; Moore, G. W. K.

    2008-10-01

    The extreme height of Mount Everest is such that its summit region may periodically be in the lower stratosphere. In this regard it provides a unique location for observing the exchange of ozone between the upper troposphere and lower stratosphere. Here we report the first surface ozone measurements from the summit region of Mount Everest. Simultaneous measurements were recorded at different elevations on the north side from base camp (5676 m) to the summit (8848 m) during May 2005. The concentrations measured were as high as 70 ppb. Meteorological diagnostics suggest that the stratosphere as well as the long range transport of polluted tropospheric air masses from South East Asia are sources of the observed ozone. There is evidence that the source region for ozone in the vicinity of Mount Everest may vary with the onset of the summer monsoon.

  13. Meteorologically-adjusted trend analysis of surface observed ozone at three monitoring sites in Delhi, India: 2007-2011

    Science.gov (United States)

    Biswas, J.; Farooqui, Z.; Guttikunda, S. K.

    2012-12-01

    It is well known that meteorological parameters have significant impact on surface ozone concentrations. Therefore it is important to remove the effects of meteorology on ozone concentrations to correctly estimate long-term trends in ozone levels due to the alterations in precursor emissions. This is important for the development of effectual control strategies. In this study surface observed ozone trends in New Delhi are analyzed using Komogorov-Zurbenko (KZ) filter, US EPA ozone adjustment due to weather approach and the classification and regression tree method. The statistical models are applied to the ozone data at three observational sites in New Delhi metropolitan areas, 1) Income Tax Office (ITO) 2) Sirifort and 3) Delhi College of Engineering (DCE). The ITO site is located adjacent to a traffic crossing, Sirifort is an urban site and the DCE site is located in a residential area. The ITO site is also influenced by local industrial emissions. DCE has higher ozone levels than the other two sites. It was found that ITO has lowest ozone concentrations amongst the three sites due to ozone titrating due to industrial and on-road mobile NOx emissions. The statistical methods employed can assess ozone trends at these sites with a high degree of confidence and the results can be used to gauge the effectiveness of control strategies on surface ozone levels in New Delhi.

  14. Description of the surface water filtration and ozone treatment system at the Northeast Fishery Center

    Science.gov (United States)

    A water filtration and ozone disinfection system was installed at the U.S. Fish and Wildlife Service's Northeast Fishery Center in Lamar, Pennsylvania to treat a surface water supply that is used to culture sensitive and endangered fish. The treatment system first passes the surface water through dr...

  15. Reaction rates of ozone and terpenes adsorbed to model indoor surfaces.

    Science.gov (United States)

    Springs, M; Wells, J R; Morrison, G C

    2011-08-01

    Reaction rates and reaction probabilities have been quantified on model indoor surfaces for the reaction of ozone with two monoterpenes (Δ(3) -carene and d-limonene). Molar surface loadings were obtained by performing breakthrough experiments in a plug-flow reactor (PFR) packed with beads of glass, polyvinylchloride or zirconium silicate. Reaction rates and probabilities were determined by equilibrating the PFR with both the terpene and the ozone and measuring the ozone consumption rate. To mimic typical indoor conditions, temperatures of 20, 25, and 30°C were used in both types of experiments along with a relative humidity ranging from 10% to 80%. The molar surface loading decreased with increased relative humidity, especially on glass, suggesting that water competed with the terpenes for adsorption sites. The ozone reactivity experiments indicate that higher surface loadings correspond with higher ozone uptake. The reaction probability for Δ(3) -carene with ozone ranged from 2.9 × 10(-6) to 3.0 × 10(-5) while reaction probabilities for d-limonene ranged from 2.8 × 10(-5) to 3.0 × 10(-4) . These surface reaction probabilities are roughly 10-100 times greater than the corresponding gas-phase values. Extrapolation of these results to typical indoor conditions suggests that surface conversion rates may be substantial relative to gas-phase rates, especially for lower volatility terpenoids. At present, it is unclear how important heterogeneous reactions will be in influencing indoor concentrations of terpenes, ozone and their reaction products. We observe that surface reaction probabilities were 10 to 100 times greater than their corresponding gas-phase values. Thus indoor surfaces do enhance effective reaction rates and adsorption of terpenes will increase ozone flux to otherwise low-reactivity surfaces. Extrapolation of these results to typical indoor conditions suggests that surface conversion rates may be substantial relative to gas-phase rates, especially

  16. Links between extreme UV-radiation, total ozone, surface albedo and cloudiness: An analysis of 30 years of data from Switzerland and Austria

    Science.gov (United States)

    Rieder, H. E.; Staehelin, J.; Weihs, P.; Vuilleumier, L.; Blumthaler, M.; Holawe, F.; Lindfors, A.; Maeder, J. A.; Simic, S.; Wagner, J. E.; Walker, D.; Ribatet, M.

    2009-04-01

    Since the discovery of anthropogenic ozone depletion in the early 1970s (e.g. Molina and Rowland, 1974; Farman et al., 1985) the interest in stratospheric ozone trends and solar UV-B increased within the scientific community and the general public because of the link between reduced total column ozone and increased UV-radiation doses. Stratospheric ozone (e.g. Koch et al., 2005) and erythemal UV-radiation (e.g. Rieder et al., 2008) in the northern mid-latitudes are characterized by strong temporal variability. Long-term measurements of UV-B radiation are rare and datasets are only available for few locations and most of these measurements do not provide spectral information on the UV part of the spectra. During strong efforts in the reconstruction of erythemal UV, datasets of past UV-radiation doses became available for several measurement sites all over the globe. For Switzerland and Austria reconstructed UV datasets are available for 3 measurement sites (Davos, Sonnblick and Vienna) (Lindfors and Vuilleumier, 2005; Rieder et al., 2008). The world's longest ozone time series dating back to 1926 is available from Arosa, Switzerland, and is discussed in detail by Staehelin et al. (1998a,b). Recently new tools from extreme value theory have been applied to the Arosa time series to describe extreme events in low and high total ozone (Rieder et al., 2009). In our study we address the question of how much of the extremes in UV-radiation can be attributed to extremes in total ozone, high surface albedo and cloudiness. An analysis of the frequency distributions of such extreme events for the last decades is presented to gain a better understanding of the links between extreme erythemal UV-radiation, total ozone, surface albedo and clouds. References: Farman, J. C., Gardiner, B. G., and Shanklin, J. D.: Large losses of total ozone in Antarctica reveal seasonal ClOx/NOx interaction, Nature, 315, 207-210, 1985. Koch, G., Wernli, H., Schwierz, C., Staehelin, J., and Peter, T

  17. Is the Ozone Hole over Your Classroom?

    Science.gov (United States)

    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…

  18. Depleting groundwater resources mitigating surface freshwater scarcity - a trend in the recent past

    Science.gov (United States)

    Wada, Y.; Van Beek, L. P.; Bierkens, M. F.

    2011-12-01

    During the past decades, human water use more than doubled, yet available surface freshwater resources are finite. As a result, water scarcity has become prevalent in many (semi-)arid regions of the world (e.g., India, Pakistan, North East China, the MENA region). In such regions, the demand often exceeds the available surface freshwater resources primarily due to heavy irrigation which requires large volumes of water in a certain time of the year, when groundwater is additionally used to supplement the deficiency. Excessive groundwater pumping, however, often leads to overexploitation, i.e. groundwater abstraction exceeding groundwater recharge. Here, we quantified globally the impact of depleting groundwater resources on mitigating surface freshwater scarcity and the trend between 1960 and 2000 at a spatial resolution of 0.5 degree. We downscaled available country statistics of groundwater abstraction to 0.5 degree, while we simulated groundwater recharge with the global hydrological model PCR-GLOBWB at the same spatial resolution considering not only natural groundwater recharge but also artificial recharge, i.e. return flow from irrigation. Water scarcity was estimated by confronting computed water demand for livestock, irrigation, industry and households with simulated surface freshwater availability (PCR-GLOBWB) at 0.5 degree. We thus performed a simulation run with/without groundwater pumping to assess the impact on alleviating surface freshwater scarcity. The results indicated that in many of (semi-)arid regions (e.g., North Wet India, North East Pakistan, North East China, West and Central USA, Central Mexico, North Iran, Central Saudi Arabia) large amounts of groundwater abstraction significantly mitigates the intensity of surface freshwater scarcity, while depleting the resources. Our estimate of global groundwater depletion reached close to 280 km3/yr. In most of the MENA region, the intensity of surface freshwater scarcity was eased by 30% up to 50% as

  19. Stratospheric ozone depletion: high arctic tundra plant species from Svalbard are not affected by enhanced UV-B after 7 years of UV-B supplementation in the field.

    NARCIS (Netherlands)

    Rozema, J.; Boelen, P.; Blokker, P.; Callaghan, T.V.; Solheim, B.; Zielke, M.

    2006-01-01

    The response of tundra plants to enhanced UV-B radiation simulating 15 and 30% ozone depletion was studied at two high arctic sites (Isdammen and Adventdalen, 78° N, Svalbard).The set-up of the UV-B supplementation systems is described, consisting of large and small UV lamp arrays, installed in 1996

  20. Stratospheric ozone depletion: high arctic tundra plant growth on Svalbard is not affected by enhanced UV-B after 7 years of UV-B supplementation in the field.

    NARCIS (Netherlands)

    Rozema, J.; Boelen, P.; Solheim, B.; Zielke, M.; Buskens, A.; Doorenbosch, M.; Fijn, R.; Herder, J.; Callaghan, T.V.; Bjorn, L.O.; Gwynn-Jones, D.; Broekman, R.A.; Blokker, P.; van de Poll, W.

    2006-01-01

    The response of tundra plants to enhanced UV-B radiation simulating 15 and 30% ozone depletion was studied at two high arctic sites (Isdammen and Adventdalen, 78° N, Svalbard).The set-up of the UV-B supplementation systems is described, consisting of large and small UV lamp arrays, installed in 1996

  1. Stratospheric ozone depletion : High arctic tundra plant growth on Svalbard is not affected by enhanced UV-B after 7 years of UV-B supplementation in the field

    NARCIS (Netherlands)

    Rozema, Jelte; Boelen, P.; Solheim, B.; Zielke, M.; Buskens, A; Doorenbosch, M.; Fijn, R.; Herder, J.; Callaghan, T.; Bjoern, L.O.; Jones, D.G.; Broekman, R.; Blokker, P.; van de Poll, W.H.

    The response of tundra plants to enhanced UV-B radiation simulating 15 and 30% ozone depletion was studied at two high arctic sites (Isdammen and Adventdalen, 78 degrees N, Svalbard).The set-up of the UV-B supplementation systems is described, consisting of large and small UV lamp arrays, installed

  2. Surface recombination of oxygen atoms in O2 plasma at increased pressure: II. Vibrational temperature and surface production of ozone

    Science.gov (United States)

    Lopaev, D. V.; Malykhin, E. M.; Zyryanov, S. M.

    2011-01-01

    Ozone production in an oxygen glow discharge in a quartz tube was studied in the pressure range of 10-50 Torr. The O3 density distribution along the tube diameter was measured by UV absorption spectroscopy, and ozone vibrational temperature TV was found comparing the calculated ab initio absorption spectra with the experimental ones. It has been shown that the O3 production mainly occurs on a tube surface whereas ozone is lost in the tube centre where in contrast the electron and oxygen atom densities are maximal. Two models were used to analyse the obtained results. The first one is a kinetic 1D model for the processes occurring near the tube walls with the participation of the main particles: O(3P), O2, O2(1Δg) and O3 molecules in different vibrational states. The agreement of O3 and O(3P) density profiles and TV calculated in the model with observed ones was reached by varying the single model parameter—ozone production probability (\\gamma_{O_{3}}) on the quartz tube surface on the assumption that O3 production occurs mainly in the surface recombination of physisorbed O(3P) and O2. The phenomenological model of the surface processes with the participation of oxygen atoms and molecules including singlet oxygen molecules was also considered to analyse \\gamma_{O_{3}} data obtained in the kinetic model. A good agreement between the experimental data and the data of both models—the kinetic 1D model and the phenomenological surface model—was obtained in the full range of the studied conditions that allowed consideration of the ozone surface production mechanism in more detail. The important role of singlet oxygen in ozone surface production was shown. The O3 surface production rate directly depends on the density of physisorbed oxygen atoms and molecules and can be high with increasing pressure and energy inputted into plasma while simultaneously keeping the surface temperature low enough. Using the special discharge cell design, such an approach opens up the

  3. Surface recombination of oxygen atoms in O2 plasma at increased pressure: II. Vibrational temperature and surface production of ozone

    International Nuclear Information System (INIS)

    Lopaev, D V; Malykhin, E M; Zyryanov, S M

    2011-01-01

    Ozone production in an oxygen glow discharge in a quartz tube was studied in the pressure range of 10-50 Torr. The O 3 density distribution along the tube diameter was measured by UV absorption spectroscopy, and ozone vibrational temperature T V was found comparing the calculated ab initio absorption spectra with the experimental ones. It has been shown that the O 3 production mainly occurs on a tube surface whereas ozone is lost in the tube centre where in contrast the electron and oxygen atom densities are maximal. Two models were used to analyse the obtained results. The first one is a kinetic 1D model for the processes occurring near the tube walls with the participation of the main particles: O( 3 P), O 2 , O 2 ( 1 Δ g ) and O 3 molecules in different vibrational states. The agreement of O 3 and O( 3 P) density profiles and T V calculated in the model with observed ones was reached by varying the single model parameter-ozone production probability (γ O 3 ) on the quartz tube surface on the assumption that O 3 production occurs mainly in the surface recombination of physisorbed O( 3 P) and O 2 . The phenomenological model of the surface processes with the participation of oxygen atoms and molecules including singlet oxygen molecules was also considered to analyse γ O 3 data obtained in the kinetic model. A good agreement between the experimental data and the data of both models-the kinetic 1D model and the phenomenological surface model-was obtained in the full range of the studied conditions that allowed consideration of the ozone surface production mechanism in more detail. The important role of singlet oxygen in ozone surface production was shown. The O 3 surface production rate directly depends on the density of physisorbed oxygen atoms and molecules and can be high with increasing pressure and energy inputted into plasma while simultaneously keeping the surface temperature low enough. Using the special discharge cell design, such an approach opens up

  4. Na-surface segregation and oxygen depletion in particle bombardment of alkaline glasses

    Energy Technology Data Exchange (ETDEWEB)

    Torrisi, A.; Marletta, G.; Licciardello, A.; Puglisi, O.

    1988-05-01

    Alkaline glass samples were bombarded by 2 keV Ar ions and neutrals and the surface modification were followed by XPS. Two main effects have been detected after bombardement: (I) a lowering of the Na/Si atomic ratio with a steady state value of about 1/2 of the initial value, and (II) an oxygen depletion. Both effects are independent of the charge state of the projectiles. The sodium concentration profile has been studied by XPS tilting angle technique and it is concluded that bombardment-induced surface segregation occurs and that it is may be responsible for the observed sodium behaviour.

  5. An Evaluation of C1-C3 Hydrochlorofluorocarbon (HCFC) Metrics: Lifetimes, Ozone Depletion Potentials, Radiative Efficiencies, Global Warming and Global Temperature Potentials

    Science.gov (United States)

    Burkholder, J. B.; Papanastasiou, D. K.; Marshall, P.

    2017-12-01

    Hydrochlorofluorocarbons (HCFCs) have been used as chlorofluorocarbon (CFC) substitutes in a number of applications, e.g. refrigerator and air-conditioning systems. Although HCFCs have lower ozone-depletion potentials (ODPs) compared to CFCs, they are potent greenhouse gases. The twenty-eighth meeting of the parties to the Montreal Protocol on Substances that Deplete the Ozone Layer (Kigali, 2016) included a list of 274 HCFCs to be controlled under the Montreal Protocol. However, from this list, only 15 of the HCFCs have values for their atmospheric lifetime, ODP, global warming potential (GWP), and global temperature potential (GTP) that are based on fundamental experimental studies, while 48 are registered compounds. In this work, we present a comprehensive evaluation of the atmospheric lifetimes, ODPs, radiative efficiencies (REs), GWPs, and GTPs for all 274 HCFCs to be included in the Montreal Protocol. Atmospheric lifetimes were estimated based on HCFC reactivity with OH radicals and O(1D), as well as their removal by UV photolysis using structure activity relationships and reactivity trends. ODP values are based on the semi-empirical approach described in the WMO/UNEP ozone assessment. Radiative efficiencies were estimated, based on infrared spectra calculated using theoretical electronic structure methods (Gaussian 09). GWPs and GTPs were calculated relative to CO2 using our estimated atmospheric lifetimes and REs. The details of the methodology will be discussed as well as the associated uncertainties. This study has provided a consistent set of atmospheric metrics for a wide range of HCFCs that support future policy decisions. More accurate metrics for a specific HCFC, if desired, would require fundamental laboratory studies to better define the OH reactivity and infrared absorption spectrum of the compound of interest. Overall, HCFCs within the same family (isomers) show a large ODP, GWP, GTP dependence on the molecular geometry of the isomers. The

  6. Characterization of surface dielectric barrier discharge influenced by intermediate frequency for ozone production

    International Nuclear Information System (INIS)

    Abdelaziz, Ayman A; Ishijima, Tatsuo; Seto, Takafumi; Otani, Yoshio; Osawa, Naoki; Wedaa, Hassan

    2016-01-01

    The aim of this study is to investigate the effect of the intermediate frequency (1–10 kHz) of the sinusoidal driving voltage on the characteristics of a developed surface dielectric barrier discharge (SDBD)-based reactor having spikes on its discharge electrode. Moreover, its influence on the production of ozone and nitrogen oxide byproducts is evaluated. The results show that SDBD is operated in the filamentary mode at all the frequencies. Nevertheless, the pulses of the discharge current at high frequencies are much denser and have higher amplitudes than those at low frequencies. The analysis of the power consumed in the reactor shows that a small portion of the input power is dissipated in the dielectric material of SDBD source, whereas the major part of the power is consumed in the plasma discharge. The results of the ozone production show that higher frequencies have a slightly adverse effect on the ozone production at relatively high energy density values, where the ozone concentration is slightly decreased when the frequency is increased at the same energy density. The temperature of the discharge channels and gas is not a crucial factor for the decomposition of ozone in this reactor, while the results of the measurements of nitrogen oxides characteristics indicate that the formation of NO and NO 2 has a significant adverse effect on the production efficiency of ozone due to their oxidation to another nitrogen oxides and their catalytic effect. (paper)

  7. How to most effectively expand the global surface ozone observing network

    Science.gov (United States)

    Sofen, E. D.; Bowdalo, D.; Evans, M. J.

    2016-02-01

    Surface ozone observations with modern instrumentation have been made around the world for more than 40 years. Some of these observations have been made as one-off activities with short-term, specific science objectives and some have been made as part of wider networks which have provided a foundational infrastructure of data collection, calibration, quality control, and dissemination. These observations provide a fundamental underpinning to our understanding of tropospheric chemistry, air quality policy, atmosphere-biosphere interactions, etc. brought together eight of these networks to provide a single data set of surface ozone observations. We investigate how representative this combined data set is of global surface ozone using the output from a global atmospheric chemistry model. We estimate that on an area basis, 25 % of the globe is observed (34 % land, 21 % ocean). Whereas Europe and North America have almost complete coverage, other continents, Africa, South America, Australia, and Asia (12-17 %) show significant gaps. Antarctica is surprisingly well observed (78 %). Little monitoring occurs over the oceans, with the tropical and southern oceans particularly poorly represented. The surface ozone over key biomes such as tropical forests and savanna is almost completely unmonitored. A chemical cluster analysis suggests that a significant number of observations are made of polluted air masses, but cleaner air masses whether over the land or ocean (especially again in the tropics) are significantly under-observed. The current network is unlikely to see the impact of the El Niño-Southern Oscillation (ENSO) but may be capable of detecting other planetary-scale signals. Model assessment and validation activities are hampered by a lack of observations in regions where the models differ substantially, as is the ability to monitor likely changes in surface ozone over the next century. Using our methodology we are able to suggest new sites which would help to close

  8. How to most effectively expand the global surface ozone observing network

    Directory of Open Access Journals (Sweden)

    E. D. Sofen

    2016-02-01

    Full Text Available Surface ozone observations with modern instrumentation have been made around the world for more than 40 years. Some of these observations have been made as one-off activities with short-term, specific science objectives and some have been made as part of wider networks which have provided a foundational infrastructure of data collection, calibration, quality control, and dissemination. These observations provide a fundamental underpinning to our understanding of tropospheric chemistry, air quality policy, atmosphere–biosphere interactions, etc. brought together eight of these networks to provide a single data set of surface ozone observations. We investigate how representative this combined data set is of global surface ozone using the output from a global atmospheric chemistry model. We estimate that on an area basis, 25 % of the globe is observed (34 % land, 21 % ocean. Whereas Europe and North America have almost complete coverage, other continents, Africa, South America, Australia, and Asia (12–17 % show significant gaps. Antarctica is surprisingly well observed (78 %. Little monitoring occurs over the oceans, with the tropical and southern oceans particularly poorly represented. The surface ozone over key biomes such as tropical forests and savanna is almost completely unmonitored. A chemical cluster analysis suggests that a significant number of observations are made of polluted air masses, but cleaner air masses whether over the land or ocean (especially again in the tropics are significantly under-observed. The current network is unlikely to see the impact of the El Niño–Southern Oscillation (ENSO but may be capable of detecting other planetary-scale signals. Model assessment and validation activities are hampered by a lack of observations in regions where the models differ substantially, as is the ability to monitor likely changes in surface ozone over the next century. Using our methodology we are able to suggest new

  9. The signs of Antarctic ozone hole recovery.

    Science.gov (United States)

    Kuttippurath, Jayanarayanan; Nair, Prijitha J

    2017-04-03

    Absorption of solar radiation by stratospheric ozone affects atmospheric dynamics and chemistry, and sustains life on Earth by preventing harmful radiation from reaching the surface. Significant ozone losses due to increases in the abundances of ozone depleting substances (ODSs) were first observed in Antarctica in the 1980s. Losses deepened in following years but became nearly flat by around 2000, reflecting changes in global ODS emissions. Here we show robust evidence that Antarctic ozone has started to recover in both spring and summer, with a recovery signal identified in springtime ozone profile and total column measurements at 99% confidence for the first time. Continuing recovery is expected to impact the future climate of that region. Our results demonstrate that the Montreal Protocol has indeed begun to save the Antarctic ozone layer.

  10. Lidar Measurements of Tropospheric Ozone in the Arctic

    Directory of Open Access Journals (Sweden)

    Seabrook Jeffrey

    2016-01-01

    Full Text Available This paper reports on differential absorption lidar (DIAL measurements of tropospheric ozone in the Canadian Arctic during springtime. Measurements at Eureka Weather Station revealed that mountains have a significant effect on the vertical structure of ozone above Ellesmere Island. Ozone depletion events were observed when air that had spent significant time near to the frozen surface of the Arctic Ocean reached Eureka. This air arrived at Eureka by flowing over the surrounding mountains. Surface level ozone depletions were not observed during periods when the flow of air from over the sea ice was blocked by mountains. In the case of blocking there was an enhancement in the amount of ozone near the surface as air from the mid troposphere descended in the lee of the mountains. Three case studies will be shown in the presentation, while one is described in this paper.

  11. Climate change impacts on projections of excess mortality at 2030 using spatially varying ozone-temperature risk surfaces.

    Science.gov (United States)

    Wilson, Ander; Reich, Brian J; Nolte, Christopher G; Spero, Tanya L; Hubbell, Bryan; Rappold, Ana G

    2017-01-01

    We project the change in ozone-related mortality burden attributable to changes in climate between a historical (1995-2005) and near-future (2025-2035) time period while incorporating a non-linear and synergistic effect of ozone and temperature on mortality. We simulate air quality from climate projections varying only biogenic emissions and holding anthropogenic emissions constant, thus attributing changes in ozone only to changes in climate and independent of changes in air pollutant emissions. We estimate non-linear, spatially varying, ozone-temperature risk surfaces for 94 US urban areas using observed data. Using the risk surfaces and climate projections we estimate daily mortality attributable to ozone exceeding 40 p.p.b. (moderate level) and 75 p.p.b. (US ozone NAAQS) for each time period. The average increases in city-specific median April-October ozone and temperature between time periods are 1.02 p.p.b. and 1.94 °F; however, the results varied by region. Increases in ozone because of climate change result in an increase in ozone mortality burden. Mortality attributed to ozone exceeding 40 p.p.b. increases by 7.7% (1.6-14.2%). Mortality attributed to ozone exceeding 75 p.p.b. increases by 14.2% (1.6 28.9%). The absolute increase in excess ozone mortality is larger for changes in moderate ozone levels, reflecting the larger number of days with moderate ozone levels.

  12. Nocturnal surface ozone enhancement over Portugal during winter: Influence of different atmospheric conditions

    KAUST Repository

    Kulkarni, Pavan S.

    2016-09-24

    Four distinct nocturnal surface ozone (NSO) enhancement events were observed, with NSO concentration exceeding 80μg/m3, at multiple ozone (O3) monitoring stations (32 sites) in January, November and December between year 2000–2010, in Portugal. The reasonable explanation for the observed bimodal pattern of surface ozone with enhanced NSO concentration during nighttime has to be transport processes, as the surface ozone production ceases at nighttime. Simultaneous measurements of O3 at multiple stations during the study period in Portugal suggest that horizontal advection alone cannot explain the observed NSO enhancement. Thus, detailed analysis of the atmospheric conditions, simulated with the Weather Research and Forecasting (WRF) model, were performed to evaluate the atmospheric mechanisms responsible for NSO enhancement in the region. Simulations revealed that each event occurred as a result of one or the combination of different atmospheric processes such as, passage of a cold front followed by a subsidence zone; passage of a moving surface trough, with associated strong horizontal wind speed and vertical shear; combination of vertical and horizontal transport at the synoptic scale; formation of a low level jet with associated vertical mixing below the jet stream. The study confirmed that large-scale flow pattern resulting in enhanced vertical mixing in the nocturnal boundary layer, plays a key role in the NSO enhancement events, which frequently occur over Portugal during winter months. © 2016 Elsevier Ltd

  13. An Evaluation of the GLOBE Surface Ozone Protocol After Five Years of Implementation

    Science.gov (United States)

    Pippin, M.; Ladd, I.; Fishman, J.

    2003-12-01

    The Surface Ozone Protocol has been a part of the GLOBE Program since 1998. Our goal has been to introduce the student to the subject of atmospheric chemistry and the relationship between air quality and other parameters such as temperature and cloud cover by providing teachers and students with a relatively accurate and inexpensive method to measure ozone. During the past five years, our group can point to both successes and disappointments. Vital elements for the successes include teacher training in data collection and analysis with integration into the core curriculum, a support structure within the schools and community to facilitate continuous data collection and reporting, quality assurance of the reported data and an open channel of communication between teachers and scientists. Once the protocol is implemented, we recognize that our GLOBE teachers require additional structure and support beyond the initial GLOBE training. Out of 57 GLOBE schools reporting ozone data, 47 schools have reported fewer than 100 data points, with 38 of those schools reporting fewer than 30 data points. However, four schools located in the Czech Republic are successfully implementing the surface ozone protocol and have reported over 500 ozone measurements with meta data providing continuous data sets over several years. We are currently developing the infrastructure for educator/community teams to facilitate year-round surface ozone measurements, and providing on-site training, follow up visits, and electronic based interactions to support the educator/community teams and students as they gather data. We present the successful strategies from the Czech Republic schools and provide suggestions for improving the involvement and retention for the U.S. schools.

  14. Depletion of barium and radium-226 in Black Sea surface waters over the past thirty years

    International Nuclear Information System (INIS)

    Kenison Falkner, K.K.; Edmond, J.M.; O'Neill, D.J.; Todd, J.F.; Moore, W.S.

    1991-01-01

    The nearly landlocked waters of the Black Sea support a valuable fishery, but are also particularly vulnerable to anthropogenic disturbance. Here we use dissolved barium and radium-226 as tracers, to investigate the biogeochemical health of the sea. Both elements are brought to surface waters by vertical mixing of deeper, enriched waters, and by rivers; these inputs should ordinarily be balanced by outflow of surface waters at the Bosphorus, and by biologically mediated removal of 226 Ra-bearing barite. We show, however, that surface-water inventories have been substantially depleted over the past few decades: recent (1988-89) barium concentrations were 1.6 times lower than in 1958 and 1967. These observations suggest that steady-state cycling of these elements has been perturbed by increased primary productivity, presumably fuelled by nutrients from industry and agricultural runoff, and to a lesser extent by decreased fluvial sediment loads owing to extensive impoundment of rivers in the region. (author)

  15. Global impacts of surface ozone changes on crop yields and land use

    Science.gov (United States)

    Chuwah, Clifford; van Noije, Twan; van Vuuren, Detlef P.; Stehfest, Elke; Hazeleger, Wilco

    2015-04-01

    Exposure to surface ozone has detrimental impacts on vegetation and crop yields. In this study, we estimate ozone impacts on crop production and subsequent impacts on land use in the 2005-2050 period using results of the TM5 atmospheric chemistry and IMAGE integrated assessment model. For the crops represented in IMAGE, we compute relative yield losses based on published exposure-response functions. We examine scenarios with either constant or declining emission factors in a weak climate policy future (radiative forcing target of 6.0 W/m2 at the end of the century), as well as co-benefits of stringent climate policy (targeted at 2.6 W/m2). Without a large decrease in air pollutant emissions, higher ozone concentrations could lead to an increase in crop damage of up to 20% locally in 2050 compared to the situation in which the changes in ozone are not accounted for. This may lead to a 2.5% global increase in crop area, and a regional increase of 8.9% in Asia. Implementation of air pollution policies could limit crop yield losses due to ozone to maximally 10% in 2050 in the most affected regions. Similar effects can be obtained as a result of co-benefits from climate policy (reducing ozone precursor emissions). We also evaluated the impact of the corresponding land-use changes on the carbon cycle. Under the worst-case scenario analysed in this study, future ozone increases are estimated to increase the cumulative net CO2 emissions between 2005 and 2050 by about 3.7 Pg C, which corresponds to about 10% of baseline land use emissions over the same period.

  16. The impact of anthropogenic and biogenic emissions on surface ozone concentrations in Istanbul.

    Science.gov (United States)

    Im, Ulas; Poupkou, Anastasia; Incecik, Selahattin; Markakis, Konstantinos; Kindap, Tayfun; Unal, Alper; Melas, Dimitros; Yenigun, Orhan; Topcu, Sema; Odman, M Talat; Tayanc, Mete; Guler, Meltem

    2011-03-01

    Surface ozone concentrations at Istanbul during a summer episode in June 2008 were simulated using a high resolution and urban scale modeling system coupling MM5 and CMAQ models with a recently developed anthropogenic emission inventory for the region. Two sets of base runs were performed in order to investigate for the first time the impact of biogenic emissions on ozone concentrations in the Greater Istanbul Area (GIA). The first simulation was performed using only the anthropogenic emissions whereas the second simulation was performed using both anthropogenic and biogenic emissions. Biogenic NMVOC emissions were comparable with anthropogenic NMVOC emissions in terms of magnitude. The inclusion of biogenic emissions significantly improved the performance of the model, particularly in reproducing the low night time values as well as the temporal variation of ozone concentrations. Terpene emissions contributed significantly to the destruction of the ozone during nighttime. Biogenic NMVOCs emissions enhanced ozone concentrations in the downwind regions of GIA up to 25ppb. The VOC/NO(x) ratio almost doubled due to the addition of biogenic NMVOCs. Anthropogenic NO(x) and NMVOCs were perturbed by ±30% in another set of simulations to quantify the sensitivity of ozone concentrations to the precursor emissions in the region. The sensitivity runs, as along with the model-calculated ozone-to-reactive nitrogen ratios, pointed NO(x)-sensitive chemistry, particularly in the downwind areas. On the other hand, urban parts of the city responded more to changes in NO(x) due to very high anthropogenic emissions. Copyright © 2010 Elsevier B.V. All rights reserved.

  17. Using satellite data to guide emission control strategies for surface ozone pollution

    Science.gov (United States)

    Jin, X.; Fiore, A. M.

    2017-12-01

    Surface ozone (O3) has adverse effects on public health, agriculture and ecosystems. As a secondary pollutant, ozone is not emitted directly. Ozone forms from two classes of precursors: NOx and VOCs. We use satellite observations of formaldehyde (a marker of VOCs) and NO2 (a marker of NOx) to identify areas which would benefit more from reducing NOx emissions (NOx-limited) versus areas where reducing VOC emissions would lead to lower ozone (VOC-limited). We use a global chemical transport model (GEOS-Chem) to develop a set of threshold values that separate the NOx-limited and VOC-limited conditions. Combining these threshold values with a decadal record of satellite observations, we find that U.S. cities (e.g. New York, Chicago) have shifted from VOC-limited to NOx-limited ozone production regimes in the warm season. This transition reflects the NOx emission controls implemented over the past decade. Increasing NOx sensitivity implies that regional NOx emission control programs will improve O3 air quality more now than it would have a decade ago.

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

    Science.gov (United States)

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

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

  19. Impact of chemical lateral boundary conditions in a regional air quality forecast model on surface ozone predictions during stratospheric intrusions

    Science.gov (United States)

    Pendlebury, Diane; Gravel, Sylvie; Moran, Michael D.; Lupu, Alexandru

    2018-02-01

    A regional air quality forecast model, GEM-MACH, is used to examine the conditions under which a limited-area air quality model can accurately forecast near-surface ozone concentrations during stratospheric intrusions. Periods in 2010 and 2014 with known stratospheric intrusions over North America were modelled using four different ozone lateral boundary conditions obtained from a seasonal climatology, a dynamically-interpolated monthly climatology, global air quality forecasts, and global air quality reanalyses. It is shown that the mean bias and correlation in surface ozone over the course of a season can be improved by using time-varying ozone lateral boundary conditions, particularly through the correct assignment of stratospheric vs. tropospheric ozone along the western lateral boundary (for North America). Part of the improvement in surface ozone forecasts results from improvements in the characterization of near-surface ozone along the lateral boundaries that then directly impact surface locations near the boundaries. However, there is an additional benefit from the correct characterization of the location of the tropopause along the western lateral boundary such that the model can correctly simulate stratospheric intrusions and their associated exchange of ozone from stratosphere to troposphere. Over a three-month period in spring 2010, the mean bias was seen to improve by as much as 5 ppbv and the correlation by 0.1 depending on location, and on the form of the chemical lateral boundary condition.

  20. A network of autonomous surface ozone monitors in Antarctica: technical description and first results

    Directory of Open Access Journals (Sweden)

    S. J.-B. Bauguitte

    2011-04-01

    Full Text Available A suite of 10 autonomous ozone monitoring units, each powered using renewable energy, was developed and built to study surface ozone in Antarctica during the International Polar Year (2007–2009. The monitoring systems were deployed in a network around the Weddell Sea sector of coastal Antarctica with a transect up onto the Antarctic Plateau. The aim was to measure for a full year, thus gaining a much-improved broader view of boundary layer ozone seasonality at different locations as well as of factors affecting the budget of surface ozone in Antarctica. Ozone mixing ratios were measured based on UV photometry using a modified version of the commercial 2B Technologies Inc. Model 202 instrument. All but one of the autonomous units measured successfully within its predefined duty cycle throughout the year, with some differences in performance dependent on power availability and ambient temperature. Mean data recovery after removal of outliers was on average 70% (range 44–83% and precision varied between 1.5 and 8 ppbv, thus was sufficiently good to resolve year-round the main ozone features of scientific interest. We conclude that, with adequate power, and noting a minor communication problem, our units would be able to operate successfully at ambient temperatures down to −60 °C. Systems such as the one described in this paper, or derivatives of it, could therefore be deployed either as local or regional networks elsewhere in the Arctic or Antarctic. Here we present technical information and first results from the experiment.

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

    Science.gov (United States)

    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

  2. Effects of surface chromium depletion on localized corrosion of alloy 825 as a high-level nuclear waste container material

    International Nuclear Information System (INIS)

    Dunn, D.S.; Sridhar, N.; Cragnolino, G.A.

    1995-01-01

    Effects of the chromium-depleted, mill-finished surface on the localized corrosion resistance of alloy 825 (UNS N08825) were investigated. Tests were conducted in solutions based on the ground water at Yucca mountain, Nevada, but with a higher concentration of chloride. Results indicated that breakdown (E p ) and repassivation (E rp ) potentials for mill-finished surfaces were more active than those for polished surfaces. Potentiodynamic polarization tests indicated pits could be initiated on the chromium-depleted surface at potentials of 220 mV SCE in a solution containing 1,000 ppm Cl - at 95 C. Potentiostatic tests identified a similar pit initiation potential for the mill-finished surface. However, under longterm potentiostatic tests, a higher potential of 300 mV SCE was needed to sustain stable pit growth beyond the chromium-depleted layer. An increase in surface roughness also was observed to decrease localized corrosion resistance of the material

  3. 1,2-Dichlorohexafluoro-Cyclobutane (1,2-c-C4F6Cl2, R-316c) a Potent Ozone Depleting Substance and Greenhouse Gas: Atmospheric Loss Processes, Lifetimes, and Ozone Depletion and Global Warming Potentials for the (E) and (Z) stereoisomers

    Science.gov (United States)

    Papadimitriou, Vassileios C.; McGillen, Max R.; Smith, Shona C.; Jubb, Aaron M.; Portmann, Robert W.; Hall, Bradley D.; Fleming, Eric L.; Jackman, Charles H.; Burkholder, James B.

    2013-01-01

    The atmospheric processing of (E)- and (Z)-1,2-dichlorohexafluorocyclobutane (1,2-c-C4F6Cl2, R-316c) was examined in this work as the ozone depleting (ODP) and global warming (GWP) potentials of this proposed replacement compound are presently unknown. The predominant atmospheric loss processes and infrared absorption spectra of the R-316c isomers were measured to provide a basis to evaluate their atmospheric lifetimes and, thus, ODPs and GWPs. UV absorption spectra were measured between 184.95 to 230 nm at temperatures between 214 and 296 K and a parametrization for use in atmospheric modeling is presented. The Cl atom quantum yield in the 193 nm photolysis of R- 316c was measured to be 1.90 +/- 0.27. Hexafluorocyclobutene (c-C4F6) was determined to be a photolysis co-product with molar yields of 0.7 and 1.0 (+/-10%) for (E)- and (Z)-R-316c, respectively. The 296 K total rate coefficient for the O(1D) + R-316c reaction, i.e., O(1D) loss, was measured to be (1.56 +/- 0.11) × 10(exp -10)cu cm/ molecule/s and the reactive rate coefficient, i.e., R-316c loss, was measured to be (1.36 +/- 0.20) × 10(exp -10)cu cm/molecule/s corresponding to a approx. 88% reactive yield. Rate coefficient upper-limits for the OH and O3 reaction with R-316c were determined to be global annually averaged lifetimes for the (E)- and (Z)-R-316c isomers were calculated using a 2-D atmospheric model to be 74.6 +/- 3 and 114.1 +/-10 years, respectively, where the estimated uncertainties are due solely to the uncertainty in the UV absorption spectra. Stratospheric photolysis is the predominant atmospheric loss process for both isomers with the O(1D) reaction making a minor, approx. 2% for the (E) isomer and 7% for the (Z) isomer, contribution to the total atmospheric loss. Ozone depletion potentials for (E)- and (Z)-R-316c were calculated using the 2-D model to be 0.46 and 0.54, respectively. Infrared absorption spectra for (E)- and (Z)-R-316c were measured at 296 K and used to estimate their

  4. Sensitivity analysis of surface ozone to emission controls in Beijing and its neighboring area during the 2008 Olympic Games.

    Science.gov (United States)

    Gao, Yi; Zhang, Meigen

    2012-01-01

    The regional air quality modeling system RAMS (regional atmospheric modeling system)-CMAQ (community multi-scale air quality modeling system) is applied to analyze temporal and spatial variations in surface ozone concentration over Beijing and its surrounding region from July to October 2008. Comparison of simulated and observed meteorological elements and concentration of nitrogen oxides (NOx) and ozone at one urban site and three rural sites during Olympic Games show that model can generally reproduce the main observed feature of wind, temperature and ozone, but NOx concentration is overestimated. Although ozone concentration decreased during Olympics, high ozone episodes occurred on 24 July and 24 August with concentration of 360 and 245 microg/m3 at Aoyuncun site, respectively. The analysis of sensitive test, with and without emission controls, shows that emission controls could reduce ozone concentration in the afternoon when ozone concentration was highest but increase it at night and in the morning. The evolution of the weather system during the ozone episodes (24 July and 24 August) indicates that hot and dry air and a stable weak pressure field intensified the production of ozone and allowed it to accumulate. Process analysis at the urban site and rural site shows that under favorable weather condition on 24 August, horizontal transport was the main contributor of the rural place and the pollution from the higher layer would be transported to the surface layer. On 24 July, as the wind velocity was smaller, the impact of transport on the rural place was not obvious.

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

    Science.gov (United States)

    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.…

  6. Regional trend analysis of surface ozone observations from monitoring networks in eastern North America, Europe and East Asia

    Science.gov (United States)

    Chang, K. L.; Petropavlovskikh, I. V.; Cooper, O. R.; Schultz, M.; Wang, T.

    2017-12-01

    Surface ozone is a greenhouse gas and pollutant detrimental to human health and crop and ecosystem productivity. The Tropospheric Ozone Assessment Report (TOAR) is designed to provide the research community with an up-to-date observation-based overview of tropospheric ozone's global distribution and trends. The TOAR Surface Ozone Database contains ozone metrics at thousands of monitoring sites around the world, densely clustered across mid-latitude North America, western Europe and East Asia. Calculating regional ozone trends across these locations is challenging due to the uneven spacing of the monitoring sites across urban and rural areas. To meet this challenge we conducted a spatial and temporal trend analysis of several TOAR ozone metrics across these three regions for summertime (April-September) 2000-2014, using the generalized additive mixed model (GAMM). Our analysis indicates that East Asia has the greatest human and plant exposure to ozone pollution among investigating regions, with increasing ozone levels through 2014. The results also show that ozone mixing ratios continue to decline significantly over eastern North America and Europe, however, there is less evidence for decreases of daytime average ozone at urban sites. The present-day spatial coverage of ozone monitors in East Asia (South Korea and Japan) and eastern North America is adequate for estimating regional trends by simply taking the average of the individual trends at each site. However the European network is more sparsely populated across its northern and eastern regions and therefore a simple average of the individual trends at each site does not yield an accurate regional trend. This analysis demonstrates that the GAMM technique can be used to assess the regional representativeness of existing monitoring networks, indicating those networks for which a regional trend can be obtained by simply averaging the trends of all individual sites and those networks that require a more

  7. Analysis of surface ozone using a recurrent neural network.

    Science.gov (United States)

    Biancofiore, Fabio; Verdecchia, Marco; Di Carlo, Piero; Tomassetti, Barbara; Aruffo, Eleonora; Busilacchio, Marcella; Bianco, Sebastiano; Di Tommaso, Sinibaldo; Colangeli, Carlo

    2015-05-01

    Hourly concentrations of ozone (O₃) and nitrogen dioxide (NO₂) have been measured for 16 years, from 1998 to 2013, in a seaside town in central Italy. The seasonal trends of O₃ and NO₂ recorded in this period have been studied. Furthermore, we used the data collected during one year (2005), to define the characteristics of a multiple linear regression model and a neural network model. Both models are used to model the hourly O₃ concentration, using, two scenarios: 1) in the first as inputs, only meteorological parameters and 2) in the second adding photochemical parameters at those of the first scenario. In order to evaluate the performance of the model four statistical criteria are used: correlation coefficient, fractional bias, normalized mean squared error and a factor of two. All the criteria show that the neural network gives better results, compared to the regression model, in all the model scenarios. Predictions of O₃ have been carried out by many authors using a feed forward neural architecture. In this paper we show that a recurrent architecture significantly improves the performances of neural predictors. Using only the meteorological parameters as input, the recurrent architecture shows performance better than the multiple linear regression model that uses meteorological and photochemical data as input, making the neural network model with recurrent architecture a more useful tool in areas where only weather measurements are available. Finally, we used the neural network model to forecast the O₃ hourly concentrations 1, 3, 6, 12, 24 and 48 h ahead. The performances of the model in predicting O₃ levels are discussed. Emphasis is given to the possibility of using the neural network model in operational ways in areas where only meteorological data are available, in order to predict O₃ also in sites where it has not been measured yet. Copyright © 2015 Elsevier B.V. All rights reserved.

  8. Changes in the surface ozone after the windstorm in 2004, in the High Tatras

    Directory of Open Access Journals (Sweden)

    Bičárová Svetlana

    2015-06-01

    Full Text Available Extreme wind event in November 2004 caused spacious destruction of slope forests in the Tatra National Park, Slovakia. Relevant changes of land cover motivated researchers to investigate damaged forest ecosystem and its response to different environmental conditions. Surface ozone (O3 is a minor but not negligible compound of the ambient air. Control strategies for the reduction of O3 precursor emissions have been applied in Europe during the last two decades. In spite of these reductions, air quality indices for O3 suggest that highland sites are more vulnerable to health and environmental risk than lowlands where mostly emissions from road transport and industry are produced. Both anthropogenic sources and biogenic precursors (BVOC from forest vegetation play a relevant role in the tropospheric photochemistry, especially at mountainous and rural locations. The parameters of air quality are measured at background station Stará Lesná in the High Tatras region since 1992 in frame of an European project EMEP. Long-term data series (1992-2013 of O3 concentrations obtained for site Stará Lesná provide specific opportunity to investigate the response of BVOC reduction on O3 variability after windstorm 2004. Evaluation of these data indicates moderate increase of annual, monthly and hourly O3 means for the period from 2005 to 2013 in comparison with the previous period 1992-2004. Temporal interpolation shows evident changes of O3 concentrations, especially ~30% increase for night hours in spring season and on the contrary ~15% decrease for daylight afternoon hours in summer season. Statistically significant changes were identified for spring months (April and May, 0-6 hours and summer months (July, 12-20 hours. Increasing O3 values in the night may be associated with the absence of BVOC for ozonolysis reaction that is one of the mechanism for O3 depletion. On the other hand, the decline of daylight O3 values in summer suggests lower O3 production

  9. Effects of trans-Eurasian transport of anthropogenic pollutants on surface ozone concentrations over China

    Science.gov (United States)

    Liu, J.; Li, X.; Mauzerall, D. L.; Emmons, L. K.; Horowitz, L. W.; Guo, Y.; Tao, S.

    2015-12-01

    Due to a lack of industrialization in Western China, surface air there was, until recently, believed to be relatively unpolluted. However, recent measurements and modeling studies have found high levels of ozone (O3) there. Based on the state-of-the-science global chemical transport model MOZART-4, we identify the origin, pathway, and mechanism of trans-Eurasian transport of air pollutants to Western China in 2000. MOZART-4 generally simulates well the observed surface O3 over inland areas of China. Simulations find surface ozone concentrations over Western China on average to be about 10 ppbv higher than Eastern China. Using sensitivity studies as well as a fully-tagged approach, we find that anthropogenic emissions from all Eurasian regions except China contribute 10-15 ppbv surface O3 over Western China, superimposed upon a 35-40 ppbv natural background. Transport from European anthropogenic sources to Northwestern China results in 2-6 ppbv O3 enhancements in spring and summer. Indian anthropogenic sources strongly influence O3 over the Tibetan Plateau during the summer monsoon. Transport of O3 originating from emissions in the Middle East occasionally reach Western China and increase surface ozone there by about 1-4 ppbv. These influences are of similar magnitude as trans-Pacific and transatlantic transport of O3 and its precursors, indicating the significance of trans-Eurasian ozone transport in hemispheric transport of air pollution. Our study further indicates that mitigation of anthropogenic emissions from Europe, the Indian subcontinent, and the Middle East could benefit public health and agricultural productivity in Western China.

  10. Ozone depleting substances and greenhouse gases HFCs, PFCs and SF{sub 6} consumption and emissions; Ozonlagsnedbrydende stoffer og drivhusgasserne HFC'er, PFC'er og SF{sub 6}. Forbrug og emissioner 2002

    Energy Technology Data Exchange (ETDEWEB)

    Sander Poulsen, T. [Planmiljoe, Veksoe Sjaelland (Denmark)

    2004-07-01

    The aim of the project is to map the 2002 Danish consumption of produced ozone depleting substances and the consumption and actual emission of the greenhouse gases HFCs, PFCs and SF{sub 6}. The inventory is performed, partly according to the guidelines recommended by IPCC (Intergovernmental Panel on Climate Change), and partly according to the method that has been used for previous mappings. The mapping is done partly in order to meet Denmark's international commitments to report and partly in order to monitor how the consumption of ozone depleting substances and the emissions of greenhouse gases develop. The mapping of ozone depleting substances includes the net consumption, meaning the amount of the imported raw materials in bulk or in drums minus any re-export of the substances in the form of raw materials. Mapping of the actual emissions of HFCs, PFCs and SF{sub 6} is done in continuation of previous greenhouse gas inventories. The inventory process is continuously improving due to development of international approved guidelines (IPCC) and the production of increasingly detailed data. (BA)

  11. Decadal changes in summertime reactive oxidized nitrogen and surface ozone over the Southeast United States

    Science.gov (United States)

    Li, Jingyi; Mao, Jingqiu; Fiore, Arlene M.; Cohen, Ronald C.; Crounse, John D.; Teng, Alex P.; Wennberg, Paul O.; Lee, Ben H.; Lopez-Hilfiker, Felipe D.; Thornton, Joel A.; Peischl, Jeff; Pollack, Ilana B.; Ryerson, Thomas B.; Veres, Patrick; Roberts, James M.; Neuman, J. Andrew; Nowak, John B.; Wolfe, Glenn M.; Hanisco, Thomas F.; Fried, Alan; Singh, Hanwant B.; Dibb, Jack; Paulot, Fabien; Horowitz, Larry W.

    2018-02-01

    Widespread efforts to abate ozone (O3) smog have significantly reduced emissions of nitrogen oxides (NOx) over the past 2 decades in the Southeast US, a place heavily influenced by both anthropogenic and biogenic emissions. How reactive nitrogen speciation responds to the reduction in NOx emissions in this region remains to be elucidated. Here we exploit aircraft measurements from ICARTT (July-August 2004), SENEX (June-July 2013), and SEAC4RS (August-September 2013) and long-term ground measurement networks alongside a global chemistry-climate model to examine decadal changes in summertime reactive oxidized nitrogen (RON) and ozone over the Southeast US. We show that our model can reproduce the mean vertical profiles of major RON species and the total (NOy) in both 2004 and 2013. Among the major RON species, nitric acid (HNO3) is dominant (˜ 42-45 %), followed by NOx (31 %), total peroxy nitrates (ΣPNs; 14 %), and total alkyl nitrates (ΣANs; 9-12 %) on a regional scale. We find that most RON species, including NOx, ΣPNs, and HNO3, decline proportionally with decreasing NOx emissions in this region, leading to a similar decline in NOy. This linear response might be in part due to the nearly constant summertime supply of biogenic VOC emissions in this region. Our model captures the observed relative change in RON and surface ozone from 2004 to 2013. Model sensitivity tests indicate that further reductions of NOx emissions will lead to a continued decline in surface ozone and less frequent high-ozone events.

  12. Investigating ozone-induced decomposition of surface-bound permethrin for conditions in aircraft cabins.

    Science.gov (United States)

    Coleman, B K; Wells, J R; Nazaroff, W W

    2010-02-01

    The reaction of ozone with permethrin can potentially form phosgene. Published evidence on ozone levels and permethrin surface concentrations in aircraft cabins indicated that significant phosgene formation might occur in this setting. A derivatization technique was developed to detect phosgene with a lower limit of detection of 2 ppb. Chamber experiments were conducted with permethrin-coated materials (glass, carpet, seat fabric, and plastic) exposed to ozone under cabin-relevant conditions (150 ppb O(3), 4.5/h air exchange rate, means of material-balance modeling indicates that the upper limit on the phosgene level in aircraft cabins resulting from this chemistry is approximately 1 microg/m(3) or approximately 0.3 ppb. It was thus determined that phosgene formation, if it occurs in aircraft cabins, is not likely to exceed relevant, health-based phosgene exposure guidelines. Phosgene formation from ozone-initiated oxidation of permethrin in the aircraft cabin environment, if it occurs, is estimated to generate levels below the California Office of Environmental Health Hazard Assessment acute reference exposure level of 4 microg/m(3) or approximately 1 ppb.

  13. Ozone production using a power modulated surface dielectric barrier discharge in dry synthetic air

    Czech Academy of Sciences Publication Activity Database

    Šimek, Milan; Pekárek, S.; Prukner, Václav

    2012-01-01

    Roč. 32, č. 4 (2012), s. 743-754 ISSN 0272-4324 R&D Projects: GA ČR(CZ) GA202/09/0176 Institutional research plan: CEZ:AV0Z20430508 Keywords : ozone * surface DBD * synthetic air * nitrogen oxides * production efficiency Subject RIV: BL - Plasma and Gas Discharge Physics Impact factor: 1.728, year: 2012 http://www.springerlink.com/content/h7p1j46381150510/fulltext. pdf

  14. Influence of Power Modulation on Ozone Production Using an AC Surface Dielectric Barrier Discharge in Oxygen

    Czech Academy of Sciences Publication Activity Database

    Šimek, Milan; Pekárek, S.; Prukner, Václav

    2010-01-01

    Roč. 30, č. 5 (2010), s. 607-617 ISSN 0272-4324 R&D Projects: GA ČR(CZ) GA202/09/0176 Institutional research plan: CEZ:AV0Z20430508 Keywords : Ozone * Surface DBD * Oxygen * Production efficiency Subject RIV: BL - Plasma and Gas Disc harge Physics Impact factor: 1.798, year: 2010 http://www.springerlink.com/content/28539775w5243513/

  15. Cadmium biosorption by ozonized activated sludge: The role of bacterial flocs surface properties and mixed liquor composition

    International Nuclear Information System (INIS)

    Laurent, Julien; Casellas, Magali; Pons, Marie-Noelle; Dagot, Christophe

    2010-01-01

    Cadmium uptake by activated sludge was studied following modifications of sludge composition and surface properties induced by ozone treatment. Ozone leads to the solubilization of sludge compounds as well as their mineralization, especially humic like substances. Small particles were formed following floc disintegration, leading to a decrease of average floc size. The study of surface properties underlined the mineralization as the number of surface binding sites decreased with the increase of ozone dose. Depending on ozone dose, cadmium uptake by activated sludge flocs was either increased or decreased. Different mechanisms were involved: below 10 mg O 3 /g TS, the increase of floc specific surface area following floc size decrease as well as the release of phosphate ions yielded an increase by 75% of cadmium uptake, due to the better availability of biosorption sites and the increase of precipitation. Inversely, at higher ozone doses, the number of biosorption sites decreased due to oxidation by ozone. Moreover, dissolved organic matter concentration increased and provided ligands for metal complexation. Cadmium uptake was therefore limited for ozone doses ranging from 10 to 16.8 mg O 3 /g TS.

  16. Stratospheric solar geoengineering without ozone loss?

    Science.gov (United States)

    Keutsch, F. N.; Keith, D.; Weisenstein, D.; Dykema, J. A.

    2016-12-01

    Injecting sulfate aerosol into the stratosphere, a form of solar geoengineering, may reduce some climate risks, but it also entails new risks including ozone loss and heating of the lower tropical stratosphere which in turn increases water vapor concentration causing additional ozone loss and surface warming. Selection of a solid aerosol such as alumina or diamond for geoengineering purposes was found to minimize stratospheric heating for a given shortwave forcing, though ozone depletion via heterogeneous surface activation remains a potential problem. Here we investigate the use of solid aerosols composed of alkaline metal salts whose surfaces would convert halogens, nitric and sulfuric acid into stable salts, reducing the ozone depletion potential of these ubiquitous stratospheric substances and preventing heterogeneous activation on the geoengineering particles. Specifically, injection of calcite (CaCO3) aerosol might reduce net radiative forcing while simultaneously increasing column ozone towards its pre-anthropogenic baseline. A radiative forcing of -1 Wm-2, for example, might be achieved with a simultaneous 3.8% increase in column ozone using 2.1 Tg yr-1 of 275 nm radius calcite aerosol with ten-fold less radiative heating compared to sulfate aerosol. Geoengineering injection of reactive alkali metal salts in combination with another high refractive index material may also enable solar geoengineering with lower risk than with sulfates.

  17. Evaluation of the flux gradient technique for measurement of ozone surface fluxes over snowpack at Summit, Greenland

    Directory of Open Access Journals (Sweden)

    F. Bocquet

    2011-10-01

    Full Text Available A multi-step procedure for investigating ozone surface fluxes over polar snow by the tower gradient method was developed and evaluated. These measurements were then used to obtain five months (April–August 2004 of turbulent ozone flux data at the Summit research camp located in the center of the Greenland ice shield. Turbulent fluxes were determined by the gradient method incorporating tower measurements of (a ozone gradients measured by commercial ultraviolet absorption analyzers, (b ambient temperature gradients using aspirated thermocouple sensors, and (c wind speed gradients determined by cup anemometers. All gradient instruments were regularly inter-compared by bringing sensors or inlets to the same measurement height. The developed protocol resulted in an uncertainty on the order of 0.1 ppbv for 30-min averaged ozone gradients that were used for the ozone flux calculations. This protocol facilitated a lower sensitivity threshold for the ozone flux determination of ∼8 × 10−3μg m−2 s−1, respectively ∼0.01 cm s−1 for the ozone deposition velocity for typical environmental conditions encountered at Summit. Uncertainty in the 30-min ozone exchange measurements (evaluated by the Monte Carlo statistical approach was on the order of 10−2 cm s−1. This uncertainty typically accounted to ~20–100% of the ozone exchange velocities that were determined. These measurements are among the most sensitive ozone deposition determinations reported to date. This flux experiment allowed for measurements of the relatively low ozone uptake rates encountered for polar snow, and thereby the study of their environmental and spring-versus-summer dependencies.

  18. 1-Bromopropane, an alternative to ozone layer depleting solvents, is dose-dependently neurotoxic to rats in long-term inhalation exposure.

    Science.gov (United States)

    Ichihara, G; Kitoh, J; Yu, X; Asaeda, N; Iwai, H; Kumazawa, T; Shibata, E; Yamada, T; Wang, H; Xie, Z; Takeuchi, Y

    2000-05-01

    1-Bromopropane has been newly introduced as an alternative to ozone layer-depleting solvents. We aimed to clarify the dose-dependent effects of 1-bromopropane on the nervous system. Forty-four Wistar male rats were randomly divided into 4 groups of 11 each. The groups were exposed to 200, 400, or 800 ppm of 1-bromopropane or only fresh air 8 h per day for 12 weeks. Grip strength of forelimbs and hind limbs, maximum motor nerve conduction velocity (MCV), and distal latency (DL) of the tail nerve were measured in 9 rats of each group every 4 weeks. The other 2 rats of each group were perfused at the end of the experiment for morphological examinations. The rats of the 800-ppm group showed poor kicking and were not able to stand still on the slope. After a 12-week exposure, forelimb grip strength decreased significantly at 800 ppm and hind limb grip strength decreased significantly at both 400 and 800 ppm or after a 12-week exposure. MCV and DL of the tail nerve deteriorated significantly at 800 ppm. Ovoid or bubble-like debris of myelin sheaths was prominent in the unraveled muscular branch of the posterior tibial nerve in the 800-ppm group. Swelling of preterminal axons in the gracile nucleus increased in a dose-dependent manner. Plasma creatine phosphokinase (CPK) decreased dose-dependently with significant changes at 400 and 800 ppm. 1-Bromopropane induced weakness in the muscle strength of rat limbs and deterioration of MCV and DL in a dose-dependent manner, with morphological changes in peripheral nerve and preterminal axon in the gracile nucleus. 1-Bromopropane may be seriously neurotoxic to humans and should thus be used carefully in the workplace.

  19. Near-surface hydrogen depletion of diamond-like carbon films produced by direct ion deposition

    Science.gov (United States)

    Markwitz, Andreas; Gupta, Prasanth; Mohr, Berit; Hübner, René; Leveneur, Jerome; Zondervan, Albert; Becker, Hans-Werner

    2016-03-01

    Amorphous atomically flat diamond-like carbon (DLC) coatings were produced by direct ion deposition using a system based on a Penning ion source, butane precursor gas and post acceleration. Hydrogen depth profiles of the DLC coatings were measured with the 15N R-NRA method using the resonant nuclear reaction 1H(15N, αγ)12C (Eres = 6.385 MeV). The films produced at 3.0-10.5 kV acceleration voltage show two main effects. First, compared to average elemental composition of the film, the near-surface region is hydrogen depleted. The increase of the hydrogen concentration by 3% from the near-surface region towards the bulk is attributed to a growth model which favours the formation of sp2 hybridised carbon rich films in the film formation zone. Secondly, the depth at which the maximum hydrogen concentration is measured increases with acceleration voltage and is proportional to the penetration depth of protons produced by the ion source from the precursor gas. The observed effects are explained by a deposition process that takes into account the contributions of ion species, hydrogen effusion and preferential displacement of atoms during direct ion deposition.

  20. Near-surface hydrogen depletion of diamond-like carbon films produced by direct ion deposition

    Energy Technology Data Exchange (ETDEWEB)

    Markwitz, Andreas, E-mail: A.Markwitz@gns.cri.nz [GNS Science, Lower Hutt (New Zealand); The MacDiarmid Institute for Advanced Materials and Nanotechnology (New Zealand); Gupta, Prasanth [GNS Science, Lower Hutt (New Zealand); The MacDiarmid Institute for Advanced Materials and Nanotechnology (New Zealand); Mohr, Berit [GNS Science, Lower Hutt (New Zealand); Hübner, René [Institute of Ion Beam Physics and Materials Research, Helmholtz-Zentrum Dresden-Rossendorf (Germany); Leveneur, Jerome; Zondervan, Albert [GNS Science, Lower Hutt (New Zealand); Becker, Hans-Werner [RUBION, Ruhr-University Bochum (Germany)

    2016-03-15

    Amorphous atomically flat diamond-like carbon (DLC) coatings were produced by direct ion deposition using a system based on a Penning ion source, butane precursor gas and post acceleration. Hydrogen depth profiles of the DLC coatings were measured with the 15N R-NRA method using the resonant nuclear reaction {sup 1}H({sup 15}N, αγ){sup 12}C (E{sub res} = 6.385 MeV). The films produced at 3.0–10.5 kV acceleration voltage show two main effects. First, compared to average elemental composition of the film, the near-surface region is hydrogen depleted. The increase of the hydrogen concentration by 3% from the near-surface region towards the bulk is attributed to a growth model which favours the formation of sp{sup 2} hybridised carbon rich films in the film formation zone. Secondly, the depth at which the maximum hydrogen concentration is measured increases with acceleration voltage and is proportional to the penetration depth of protons produced by the ion source from the precursor gas. The observed effects are explained by a deposition process that takes into account the contributions of ion species, hydrogen effusion and preferential displacement of atoms during direct ion deposition.

  1. Influences of the variation in inflow to East Asia on surface ozone over Japan during 1996–2005

    Directory of Open Access Journals (Sweden)

    S. Chatani

    2011-08-01

    Full Text Available Air quality simulations in which the global chemical transport model CHASER and the regional chemical transport model WRF/chem are coupled have been developed to consider the dynamic transport of chemical species across the boundaries of the domain of the regional chemical transport model. The simulation captures the overall seasonal variations of surface ozone, but overestimates its concentration over Japanese populated areas by approximately 20 ppb from summer to early winter. It is deduced that ozone formation around Northeast China and Japan in summer is overestimated in the simulation. On the other hand, the simulation well reproduces the interannual variability and the long-term trend of observed surface ozone over Japan. Sensitivity experiments have been performed to investigate the influence of the variation in inflow to East Asia on the interannual variability and the long-term trend of surface ozone over Japan during 1996–2005. The inflow defined in this paper includes the recirculation of species with sources within the East Asian region as well as the transport of species with sources out of the East Asian region. Results of sensitivity experiments suggest that inflow to East Asia accounts for approximately 30 % of the increasing trend of surface ozone, whereas it has much less influence on the interannual variability of observed surface ozone compared to meteorological processes within East Asia.

  2. The effect of ozone on nicotine desorption from model surfaces:evidence for heterogeneous chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Destaillats, Hugo; Singer, Brett C.; Lee, Sharon K.; Gundel, LaraA.

    2005-05-01

    Assessment of secondhand tobacco smoke exposure using nicotine as a tracer or biomarker is affected by sorption of the alkaloid to indoor surfaces and by its long-term re-emission into the gas phase. However, surface chemical interactions of nicotine have not been sufficiently characterized. Here, the reaction of ozone with nicotine sorbed to Teflon and cotton surfaces was investigated in an environmental chamber by monitoring nicotine desorption over a week following equilibration in dry or humid air (65-70 % RH). The Teflon and cotton surfaces had N{sub 2}-BET surface areas of 0.19 and 1.17 m{sup 2} g{sup -1}, and water mass uptakes (at 70 % RH) of 0 and 7.1 % respectively. Compared with dry air baseline levels in the absence of O{sub 3}, gas phase nicotine concentrations decrease, by 2 orders of magnitude for Teflon after 50 h at 20-45 ppb O{sub 3}, and by a factor of 10 for cotton after 100 h with 13-15 ppb O{sub 3}. The ratios of pseudo first-order rate constants for surface reaction (r) to long-term desorption (k) were r/k = 3.5 and 2.0 for Teflon and cotton surfaces, respectively. These results show that surface oxidation was competitive with desorption. Hence, oxidative losses could significantly reduce long-term re-emissions of nicotine from indoor surfaces. Formaldehyde, N-methylformamide, nicotinaldehyde and cotinine were identified as oxidation products, indicating that the pyrrolidinic N was the site of electrophilic attack by O{sub 3}. The presence of water vapor had no effect on the nicotine-O{sub 3} reaction on Teflon surfaces. By contrast, nicotine desorption from cotton in humid air was unaffected by the presence of ozone. These observations are consistent with complete inhibition of ozone-nicotine surface reactions in an aqueous surface film present in cotton but not in Teflon surfaces.

  3. Study of an Ozone Composing Mechanism derived from the Third Element on Surface of Electrode using Oxygen Gas: Part 2

    Science.gov (United States)

    Murai, Akira; Nakajima, Tsuyoshi

    In our third experiment, we changed the density of nitrogen through the addition of heat energy to the anode. A computer simulation confirmed the same phenomenon. Then the copper anode was replaced with an antimony anode. We found that antimony worked better than nitrogen as a third element. Finally, in the fourth experiment, we used an industrial ozone generator including ceramic dielectrics and a titanium expanded metal electrode. A decrease in the temperature of the cooling water led to a proportional increase in ozone. It follows the formula of van't Hoff. After spattering the surface of the electrodes with argon gas and supplying the ozone generator with 99% oxygen, we were able to produce ozone which was more than 20% higher in concentration than primary state ozone under the same conditions. The ozone generator produced ozone in high yield efficiency due to the optimum density of a third element like nitrogen on the surface of the electrodes. Antimony works better than nitrogen does as a third element.

  4. Surface Ozone Enrichment Downwind of Manaus City, in Central Amazonia

    Science.gov (United States)

    Carbone, S.; Rizzo, L. V.; Rodrigues, N. P.; Brito, J.; Cirino, G. G.; Souza, R. A. F. D.; Barbosa, H. M.; Artaxo, P.; Martin, S. T.

    2015-12-01

    Amazonia is a unique place to study the impact of anthropogenic emissions on atmospheric photochemistry, fueled by large inputs of solar radiation, humidity, biogenic emissions and turbulent mixing. In the wet season, thousands of km2 of Amazonian forest areas can be considered pristine, whereas in the dry season biomass burning emissions in regional scale add to picture. The Amazon region is also going through localized urban development, in particular, the Manaus city, with 2 million inhabitants. The GoAmazon2014/5 experiment seeks to understand the interactions between urban and biogenic emissions in Amazonia. The combination of biogenic volatile organic compounds and urban NOx emissions is expected to increase tropospheric O3 production, with impacts to the ecosystem and human health. To investigate this issue, surface O3 measurements were taken between Feb and Dec 2014 at two sites in Amazonia: T2, located in the outflow of the Manaus urban plume, and T3, sitting 60 km downwind of the city. The influence of the urban plume at T3 site was detected by a combination of typical ΔCN/ΔCO ratios, Hysplit backtrajectories and threshold concentrations of tracers such as particle number and black carbon. The transport from T2 to T3 typically lasted 7 hours. At T2, the O3 diurnal cycle showed a diurnal peak of 20 ppb in the wet season and of 35 ppb in the dry season, suggesting the contribution of regional biomass burning to O3 photochemical production. In the absence of urban or biomass burning emissions, O3 diurnal cycle at T3 showed a peak of 15 ppb, similar to observations taken in pristine forest areas in Amazonia. When the Manaus plume reached the T3 site in the afternoon, the diurnal O3 peak increased to 40 ppb, indicating a net O3 production rate of 3.6 ppb h-1 along this diurnal transport. When the Manaus plume reached the T3 site before sunrise, i.e., a transport during the night, the diurnal peak was anticipated and reached 25 ppb.

  5. MILD CHOLESTEROL DEPLETION REDUCES AMYLOID-β PRODUCTION BY IMPAIRING APP TRAFFICKING TO THE CELL SURFACE

    Science.gov (United States)

    Guardia-Laguarta, Cristina; Coma, Mireia; Pera, Marta; Clarimón, Jordi; Sereno, Lidia; Agulló, José M.; Molina-Porcel, Laura; Gallardo, Eduard; Deng, Amy; Berezovska, Oksana; Hyman, Bradley T.; Blesa, Rafael; Gómez-Isla, Teresa; Lleó, Alberto

    2009-01-01

    It has been suggested that cellular cholesterol levels can modulate the metabolism of the amyloid precursor protein (APP) but the underlying mechanism remains controversial. In the current study, we investigate in detail the relationship between cholesterol reduction, APP processing and γ-secretase function in cell culture studies. We found that mild membrane cholesterol reduction led to a decrease in Aβ40 and Aβ42 in different cell types. We did not detect changes in APP intracellular domain or Notch intracellular domain generation. Western blot analyses showed a cholesterol-dependent decrease in the APP C-terminal fragments and cell surface APP. Finally, we applied a fluorescence resonance energy transfer (FRET)-based technique to study APP-Presenilin 1 (PS1) interactions and lipid rafts in intact cells. Our data indicate that cholesterol depletion reduces association of APP into lipid rafts and disrupts APP-PS1 interaction. Taken together, our results suggest that mild membrane cholesterol reduction impacts the cleavage of APP upstream of γ-secretase and appears to be mediated by changes in APP trafficking and partitioning into lipid rafts. PMID:19457132

  6. OZONE PRODUCTION EFFICIENCY AND NOX DEPLETION IN AN URBAN PLUME: INTERPRETATION OF FIELD OBSERVATIONS AND IMPLICATIONS FOR EVALUATING O3-NOX-VOC SENSITIVITY

    Science.gov (United States)

    Ozone production efficiency (OPE) can be defined as the number of ozone (O3) molecules photochemically produced by a molecule of NOx (NO + NO2) before it is lost from the NOx - O3 cycle. Here, we consider observational and modeling techniques to evaluate various operational defi...

  7. Global Surface Ozone Variability and Trends - The TOAR database and metrics products

    Science.gov (United States)

    Schultz, Martin

    2017-04-01

    In the context of the first Tropospheric Ozone Assessment Report (TOAR) the world's largest collection of surface ozone data has been assembled in a database at Forschungszentrum Juelich, Germany. Data span the period from 1970 to 2014. Station metadata have been harmonized and extended with information from several global high-resolution datasets. This allows for a first, globally uniform station characterisation as "urban" or "rural". Extensive quality control of the metadata and data was performed and feedback provided to original data providers. This harmonized database was then used to generate hundreds of aggregated aggregate statistics and ozone metrics for use in the analysis of trends in human health, vegetation, and climate impact assessments. These data products form the core data of the TOAR publications which shall become available as a special journal issue in October 2017. The presentation will provide an overview about the TOAR database and the TOAR data files, and demonstrate how they can be accessed and used. The potential for future developments will be discussed.

  8. Surface ozone seasonality under global change: Influence from dry deposition and isoprene emissions at northern mid-latitudes

    Science.gov (United States)

    Clifton, O.; Paulot, F.; Fiore, A. M.; Horowitz, L. W.; Malyshev, S.; Shevliakova, E.; Correa, G. J. P.; Lin, M.

    2017-12-01

    Identifying the contributions of nonlinear chemistry and transport to observed surface ozone seasonal cycles over land using global models relies on an accurate representation of ozone uptake by vegetation (dry deposition). It is well established that in the absence of ozone precursor emission changes, a warming climate will increase surface ozone in polluted regions, and that a rise in temperature-dependent isoprene emissions would exacerbate this "climate penalty". However, the influence of changes in ozone dry deposition, expected to evolve with climate and land use, is often overlooked in air quality projections. With a new scheme that represents dry deposition within the NOAA GFDL dynamic vegetation land model (LM3) coupled to the NOAA GFDL atmospheric chemistry-climate model (AM3), we simulate the impact of 21st century climate and land use on ozone dry deposition and isoprene emissions. This dry deposition parameterization is a version of the Wesely scheme, but uses parameters explicitly calculated by LM3 that respond to climate and land use (e.g., stomatal conductance, canopy interception of water, leaf area index). The parameterization includes a nonstomatal deposition dependence on humidity. We evaluate climatological present-day seasonal cycles of ozone deposition velocities and abundances with those observed at northern mid-latitude sites. With a set of 2010s and 2090s decadal simulations under a high climate warming scenario (RCP8.5) and a sensitivity simulation with well-mixed greenhouse gases following RCP8.5 but air pollutants held at 2010 levels (RCP8.5_WMGG), we examine changes in surface ozone seasonal cycles. We build on our previous findings, which indicate that strong reductions in anthropogenic NOx emissions under RCP8.5 cause the surface ozone seasonal cycle over the NE USA to reverse, shifting from a summer peak at present to a winter peak by 2100. Under RCP8.5_WMGG, we parse the separate effects of climate and land use on ozone dry

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

    Science.gov (United States)

    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.

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

    Directory of Open Access Journals (Sweden)

    W. T. Ball

    2018-02-01

    Full Text Available 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.

  11. Impact of high-resolution sea surface temperature, emission spikes and wind on simulated surface ozone in Houston, Texas during a high ozone episode

    Science.gov (United States)

    Pan, Shuai; Choi, Yunsoo; Jeon, Wonbae; Roy, Anirban; Westenbarger, David A.; Kim, Hyun Cheol

    2017-03-01

    Model-measurement comparisons for surface ozone often show significant error, which could be attributed to problems in meteorology and emissions fields. A WRF-SMOKE-CMAQ air quality modeling system was used to investigate the contributions of these inputs. In this space, a base WRF run (BASE) and a WRF run initializing with NOAA GOES satellite sea surface temperature (SST) (SENS) were performed to clarify the impact of high-resolution SST on simulated surface ozone (O3) over the Greater Houston area during 25 September 2013, corresponding to the high O3 episode during the NASA DISCOVER-AQ Texas campaign. The SENS case showed reduced land-sea thermal contrast during early morning hours due to 1-2 °C lower SST over water bodies. The lowered SST reduced the model wind speed and slowed the dilution rate. These changes led to a simulated downwind O3 change of ∼5 ppb near the area over land with peak simulated afternoon O3. However, the SENS case still under-predicted surface O3 in urban and industrial areas. Episodic flare emissions, dry sunny postfrontal stagnated conditions, and land-bay/sea breeze transitions could be the potential causes of the high O3. In order to investigate the additional sources of error, three sensitivity simulations were performed for the high ozone time period. These involved adjusted emissions, adjusted wind fields, and both adjusted emissions and winds. These scenarios were superimposed on the updated SST (SENS) case. Adjusting NOx and VOC emissions using simulated/observed ratios improved correlation and index of agreement (IOA) for NOx from 0.48 and 0.55 to 0.81 and 0.88 respectively, but still reported spatial misalignment of afternoon O3 hotspots. Adjusting wind fields to represent morning weak westerly winds and afternoon converging zone significantly mitigated under-estimation of the observed O3 peak. For example, simulations with adjusted wind fields and adjusted (emissions + wind fields) reduced under-estimation of the peak

  12. Wildfire influences on the variability and trend of summer surface ozone in the mountainous western United States

    Directory of Open Access Journals (Sweden)

    X. Lu

    2016-11-01

    Full Text Available Increasing wildfire activities in the mountainous western US may present a challenge for the region to attain a recently revised ozone air quality standard in summer. Using current Eulerian chemical transport models to examine the wildfire ozone influences is difficult due to uncertainties in fire emissions, inadequate model chemistry, and resolution. Here we quantify the wildfire influence on the ozone variability, trends, and number of high MDA8 (daily maximum 8 h average ozone days over this region in summers (June, July, and August 1989–2010 using a new approach. We define a fire index using retroplumes (plumes of back-trajectory particles computed by a Lagrangian dispersion model (FLEXPART and develop statistical models based on the fire index and meteorological parameters to interpret MDA8 ozone concentrations measured at 13 Intermountain West surface sites. We show that the statistical models are able to capture the ozone enhancements by wildfires and give results with some features different from the GEOS-Chem Eulerian chemical transport model. Wildfires enhance the Intermountain West regional summer mean MDA8 ozone by 0.3–1.5 ppbv (daily episodic enhancements reach 10–20 ppbv at individual sites with large interannual variability, which are strongly correlated with the total MDA8 ozone. We find large fire impacts on the number of exceedance days; for the 13 CASTNet sites, 31 % of the summer days with MDA8 ozone exceeding 70 ppbv would not occur in the absence of wildfires.

  13. Understanding Long-Term Variations in Surface Ozone in United States (U.S. National Parks

    Directory of Open Access Journals (Sweden)

    Deborah McGlynn

    2018-03-01

    Full Text Available Long-term surface ozone observations at 25 National Park Service sites across the United States were analyzed for processes on varying time scales using a time scale decomposition technique, the Ensemble Empirical Mode Decomposition (EEMD. Time scales of interest include the seasonal cycle, large-scale climate oscillations, and long-term (>10 years trends. Emission reductions were found to have a greater impact on sites that are nearest major urban areas. Multidecadal trends in surface ozone were increasing at a rate of 0.07 to 0.37 ppbv year−1 before 2004 and decreasing at a rate of −0.08 to −0.60 ppbv year−1 after 2004 for sites in the East, Southern California, and Northwestern Washington. Sites in the Intermountain West did not experience a reversal of trends from positive to negative until the mid- to late 2000s. The magnitude of the annual amplitude (=annual maximum–minimum decreased at eight sites, two in the West, two in the Intermountain West, and four in the East, by 5–20 ppbv and significantly increased at three sites; one in Alaska, one in the West, and one in the Intermountain West, by 3–4 ppbv. Stronger decreases in the annual amplitude occurred at a greater proportion of sites in the East (4/6 sites than in the West/Intermountain West (4/19 sites. The date of annual maximums and/or minimums has changed at 12 sites, occurring 10–60 days earlier in the year. There appeared to be a link between the timing of the annual maximum and the decrease in the annual amplitude, which was hypothesized to be related to a decrease in ozone titration resulting from NOx emission reductions. Furthermore, it was found that a phase shift of the Pacific Decadal Oscillation (PDO, from positive to negative, in 1998–1999 resulted in increased occurrences of La Niña-like conditions. This shift had the effect of directing more polluted air masses from East Asia to higher latitudes over the North American continent. The change in the

  14. Efforts to reduce stratospheric ozone loss affect agriculture

    International Nuclear Information System (INIS)

    Weare, B.C.

    1995-01-01

    Research has shown that the increased ultraviolet radiation reaching the Earth's surface resulting from stratospheric ozone loss poses a danger to everyone. Concern about ozone loss prompted many nations to ratify the Montreal Protocol, the most comprehensive international environmental agreement ever enacted. Several provisions of this protocol will have substantial, long-term effects on the agricultural industry. Agriculture contributes substantially to ozone depletion, primarily through its use of chlorofluorocarbons (CFCs) for refrigeration in processing, storage and transport of meats and produce. This paper is meant to serve as an overview of the scientific basis for ozone depletion concerns, a description of the current international policy agreement, and the possible consequences of that policy for agriculture. (author)

  15. Impact of climate change on surface ozone and deposition of sulphur and nitrogen in Europe

    Energy Technology Data Exchange (ETDEWEB)

    Langner, J.; Bergstroem, R.; Foltescu, V. [Swedish Meteorological and Hydrological Institute, Norrkoeping (Sweden)

    2005-02-01

    The potential impact of regional climate change on the distribution and deposition of air pollutants in Europe has been studied using a regional chemistry/transport/deposition model, MATCH. MATCH was set up using meteorological output from two 10-year climate change experiments made with the Rossby Centre regional Atmospheric climate model version 1 (RCA1). RCA1 was forced by boundary conditions from two different global climate models using the IPCC IS92a (business as usual) emission scenario. The global mean warming in both the GCMs was 2.6 K and was reached in the period 2050-2070. Simulations with MATCH indicate substantial potential impact of regional climate change on both deposition of oxidised nitrogen and concentrations of surface ozone. The simulations show a strong increase in surface ozone expressed as AOT40 and mean of daily maximum over southern and central Europe and a decrease in northern Europe. The simulated changes in April-September AOT40 are significant in relation to inter-annual variability over extended areas. Changes in deposition of oxidised nitrogen are much smaller and also less coherent due to the strong inter-annual variability in precipitation in the RCA1 simulations and differences in the regional climate change simulated with RCA1 in the two regional scenarios. Changes in simulated annual deposition are significant in relation to inter-annual variability only over small areas. This indicates that longer simulation periods are necessary to establish changes in deposition. (author)

  16. Impact of climate change on surface ozone and deposition of sulphur and nitrogen in Europe

    Science.gov (United States)

    Langner, Joakim; Bergström, Robert; Foltescu, Valentin

    The potential impact of regional climate change on the distribution and deposition of air pollutants in Europe has been studied using a regional chemistry/transport/deposition model, MATCH. MATCH was set up using meteorological output from two 10-year climate change experiments made with the Rossby Centre regional Atmospheric climate model version 1 (RCA1). RCA1 was forced by boundary conditions from two different global climate models using the IPCC IS92a (business as usual) emission scenario. The global mean warming in both the GCMs was 2.6 K and was reached in the period 2050-2070. Simulations with MATCH indicate substantial potential impact of regional climate change on both deposition of oxidised nitrogen and concentrations of surface ozone. The simulations show a strong increase in surface ozone expressed as AOT40 and mean of daily maximum over southern and central Europe and a decrease in northern Europe. The simulated changes in April-September AOT40 are significant in relation to inter-annual variability over extended areas. Changes in deposition of oxidised nitrogen are much smaller and also less coherent due to the strong inter-annual variability in precipitation in the RCA1 simulations and differences in the regional climate change simulated with RCA1 in the two regional scenarios. Changes in simulated annual deposition are significant in relation to inter-annual variability only over small areas. This indicates that longer simulation periods are necessary to establish changes in deposition.

  17. Reanalysis of and attribution to near-surface ozone concentrations in Sweden during 1990-2013

    Science.gov (United States)

    Andersson, Camilla; Alpfjord, Heléne; Robertson, Lennart; Karlsson, Per Erik; Engardt, Magnuz

    2017-11-01

    We have constructed two data sets of hourly resolution reanalyzed near-surface ozone (O3) concentrations for the period 1990-2013 for Sweden. Long-term simulations from a chemistry-transport model (CTM) covering Europe were combined with hourly ozone concentration observations at Swedish and Norwegian background measurement sites using retrospective variational data analysis. The reanalysis data sets show improved performance over the original CTM when compared to independent observations. In one of the reanalyses, we included all available hourly near-surface O3 observations, whilst in the other we carefully selected time-consistent observations. Based on the second reanalysis we investigated statistical aspects of the distribution of the near-surface O3 concentrations, focusing on the linear trend over the 24-year period. We show that high near-surface O3 concentrations are decreasing and low O3 concentrations are increasing, which is reflected in observed improvement of many health and vegetation indices (apart from those with a low threshold). Using the CTM we also conducted sensitivity simulations to quantify the causes of the observed change, focusing on three factors: change in hemispheric background concentrations, meteorology and anthropogenic emissions. The rising low concentrations of near-surface O3 in Sweden are caused by a combination of all three factors, whilst the decrease in the highest O3 concentrations is caused by European O3 precursor emissions reductions. While studying the impact of anthropogenic emissions changes, we identified systematic differences in the modeled trend compared to observations that must be caused by incorrect trends in the utilized emissions inventory or by too high sensitivity of our model to emissions changes.

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

    Science.gov (United States)

    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.

  19. Mortality tradeoff between air quality and skin cancer from changes in stratospheric ozone

    Science.gov (United States)

    Eastham, Sebastian D.; Keith, David W.; Barrett, Steven R. H.

    2018-03-01

    Skin cancer mortality resulting from stratospheric ozone depletion has been widely studied. Similarly, there is a deep body of literature on surface ozone and its health impacts, with modeling and observational studies demonstrating that surface ozone concentrations can be increased when stratospheric air mixes to the Earth’s surface. We offer the first quantitative estimate of the trade-off between these two effects, comparing surface air quality benefits and UV-related harms from stratospheric ozone depletion. Applying an idealized ozone loss term in the stratosphere of a chemistry-transport model for modern-day conditions, we find that each Dobson unit of stratospheric ozone depletion results in a net decrease in the global annual mortality rate of ~40 premature deaths per billion population (d/bn/DU). The impacts are spatially heterogeneous in sign and magnitude, composed of a reduction in premature mortality rate due to ozone exposure of ~80 d/bn/DU concentrated in Southeast Asia, and an increase in skin cancer mortality rate of ~40 d/bn/DU, mostly in Western Europe. This is the first study to quantify air quality benefits of stratospheric ozone depletion, and the first to find that marginal decreases in stratospheric ozone around modern-day values could result in a net reduction in global mortality due to competing health impact pathways. This result, which is subject to significant methodological uncertainty, highlights the need to understand the health and environmental trade-offs involved in policy decisions regarding anthropogenic influences on ozone chemistry over the 21st century.

  20. Effective UV/Ozone irradiation method for decontamination of hydroxyapatite surfaces

    Directory of Open Access Journals (Sweden)

    Keisuke Yasuda

    2017-08-01

    Full Text Available The purpose of this study was to establish whether UV/ozone (O3 irradiation method can effectively decontaminate hydroxyapatite surfaces, including those modified by the treatment with 30% phosphoric acid solution through morphological and chemical surface analyses (surface roughness, X-ray photoelectron spectroscopy and wettability, and to evaluate the in vitro response of osteoblast-like MC3T3-E1 cells to the modified hydroxyapatite surface decontaminated via this method. The amount of carbon and the contact angle of hydroxyapatite surfaces were significantly decreased by UV/O3 irradiation that lasted for ≥ 5 and ≥ 3 min, respectively (P 0.05. MC3T3-E1 cell proliferation, differentiation (as assessed by relative ALP and OCN mRNA levels, and mineralisation were significantly promoted on irradiated surfaces (P < 0.05. These findings show that UV/O3 irradiation for ≥ 5 min significantly decontaminated H3PO4-modified hydroxyapatite surface, improved its wettability, and facilitated osteoblast growth and function.

  1. Ozone, Climate, and Global Atmospheric Change.

    Science.gov (United States)

    Levine, Joel S.

    1992-01-01

    Presents an overview of global atmospheric problems relating to ozone depletion and global warming. Provides background information on the composition of the earth's atmosphere and origin of atmospheric ozone. Describes causes, effects, and evidence of ozone depletion and the greenhouse effect. A vignette provides a summary of a 1991 assessment of…

  2. Other EPA Initiatives to Protect the Ozone Layer

    Science.gov (United States)

    Access information on EPA's efforts to address ozone layer depletion through voluntary partnerships with the private sector and activities aimed at educating the public about the health effects of ozone layer depletion.

  3. Changes in stratospheric ozone.

    Science.gov (United States)

    Cicerone, R J

    1987-07-03

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

  4. Interactive ozone and methane chemistry in GISS-E2 historical and future climate simulations

    Directory of Open Access Journals (Sweden)

    D. T. Shindell

    2013-03-01

    Full Text Available The new generation GISS climate model includes fully interactive chemistry related to ozone in historical and future simulations, and interactive methane in future simulations. Evaluation of ozone, its tropospheric precursors, and methane shows that the model captures much of the large-scale spatial structure seen in recent observations. While the model is much improved compared with the previous chemistry-climate model, especially for ozone seasonality in the stratosphere, there is still slightly too rapid stratospheric circulation, too little stratosphere-to-troposphere ozone flux in the Southern Hemisphere and an Antarctic ozone hole that is too large and persists too long. Quantitative metrics of spatial and temporal correlations with satellite datasets as well as spatial autocorrelation to examine transport and mixing are presented to document improvements in model skill and provide a benchmark for future evaluations. The difference in radiative forcing (RF calculated using modeled tropospheric ozone versus tropospheric ozone observed by TES is only 0.016 W m−2. Historical 20th Century simulations show a steady increase in whole atmosphere ozone RF through 1970 after which there is a decrease through 2000 due to stratospheric ozone depletion. Ozone forcing increases throughout the 21st century under RCP8.5 owing to a projected recovery of stratospheric ozone depletion and increases in methane, but decreases under RCP4.5 and 2.6 due to reductions in emissions of other ozone precursors. RF from methane is 0.05 to 0.18 W m−2 higher in our model calculations than in the RCP RF estimates. The surface temperature response to ozone through 1970 follows the increase in forcing due to tropospheric ozone. After that time, surface temperatures decrease as ozone RF declines due to stratospheric depletion. The stratospheric ozone depletion also induces substantial changes in surface winds and the Southern Ocean circulation, which may play a role in

  5. Evolution of the eastward shift in the quasi-stationary minimum of the Antarctic total ozone column

    Science.gov (United States)

    Grytsai, Asen; Klekociuk, Andrew; Milinevsky, Gennadi; Evtushevsky, Oleksandr; Stone, Kane

    2017-02-01

    The quasi-stationary pattern of the Antarctic total ozone has changed during the last 4 decades, showing an eastward shift in the zonal ozone minimum. In this work, the association between the longitudinal shift of the zonal ozone minimum and changes in meteorological fields in austral spring (September-November) for 1979-2014 is analyzed using ERA-Interim and NCEP-NCAR reanalyses. Regressive, correlative and anomaly composite analyses are applied to reanalysis data. Patterns of the Southern Annular Mode and quasi-stationary zonal waves 1 and 3 in the meteorological fields show relationships with interannual variability in the longitude of the zonal ozone minimum. On decadal timescales, consistent longitudinal shifts of the zonal ozone minimum and zonal wave 3 pattern in the middle-troposphere temperature at the southern midlatitudes are shown. Attribution runs of the chemistry-climate version of the Australian Community Climate and Earth System Simulator (ACCESS-CCM) model suggest that long-term shifts of the zonal ozone minimum are separately contributed by changes in ozone-depleting substances and greenhouse gases. As is known, Antarctic ozone depletion in spring is strongly projected on the Southern Annular Mode in summer and impacts summertime surface climate across the Southern Hemisphere. The results of this study suggest that changes in zonal ozone asymmetry accompanying ozone depletion could be associated with regional climate changes in the Southern Hemisphere in spring.

  6. Optical spectroscopy analysis of the near surface depletion layer in AlGaAs/GaAs heterostructures grown by MBE

    Science.gov (United States)

    Cortes-Mestizo, I. E.; Briones, E.; Yee-Rendón, C. M.; Zamora Peredo, L.; Espinosa-Vega, L. I.; Droopad, R.; Méndez-García, Victor H.

    2017-11-01

    In this work the effects of filling the surface energy states in AlGaAs/GaAs heterostructures on the depletion layer are reported. The depletion layer width was varied from 49 to 10 nm as determined by Raman spectroscopy, allowing to discern their effect on the generation of Franz-Keldysh oscillations observed by photoreflectance spectroscopy. It is found that the photoreflectance modulation process of built-in electric fields at surface is negligible when the surface-levels are filled. This work demonstrates the relationship between the surface-states density, the surface states capability of capture carriers and the layer sequence of the heterostructure. These parameters need to be considered in order to get an adequate analysis of the photoreflectance spectrum of heterostructures. It is shown that if a nearly full-filled condition in the available surface energy levels is established, the Franz-Keldysh oscillations produced by the modulation of the built-in electric field intensity disappears as a result of the reduction in the photogenerated carrier density in the photoreflectance measurement.

  7. Ultraviolet light and ozone surface modification of poly-alpha α-methylstyrene using electroless nickel plating

    International Nuclear Information System (INIS)

    Chi Fangting; Sichuan Univ., Chengdu; Li Bo; Liu Yiyang; Chen Sufen; Jiang Bo

    2009-01-01

    The deposition capability of nickel on the surface of poly-α-methylstyrene microspheres was improved by combined treatment of ozone aeration and UV irradiation in aqueous ammonia. Surface properties of the treated film were investigated by X-ray photoelectron spectroscopy(XPS) and Fourier transform infrared(FT-TR) measurements. The samples were characterized by SEM. The results indicate that after ultraviolet joint ozone treatment, the surfaces of microspheres were oxidized, and the amine and amide groups are introduced on their surface. The images of SEM show the adhesion between microspheres and nickel-phosphorus films was improved after surface modification. This was attributed to amide which could chemisorb palladium ions to catalyze electroless nickel plating on the pretreated surface of microspheres. (authors)

  8. Impacts of stratospheric sulfate geoengineering on tropospheric ozone

    Directory of Open Access Journals (Sweden)

    L. Xia

    2017-10-01

    Full Text Available A range of solar radiation management (SRM techniques has been proposed to counter anthropogenic climate change. Here, we examine the potential effects of stratospheric sulfate aerosols and solar insolation reduction on tropospheric ozone and ozone at Earth's surface. Ozone is a key air pollutant, which can produce respiratory diseases and crop damage. Using a version of the Community Earth System Model from the National Center for Atmospheric Research that includes comprehensive tropospheric and stratospheric chemistry, we model both stratospheric sulfur injection and solar irradiance reduction schemes, with the aim of achieving equal levels of surface cooling relative to the Representative Concentration Pathway 6.0 scenario. This allows us to compare the impacts of sulfate aerosols and solar dimming on atmospheric ozone concentrations. Despite nearly identical global mean surface temperatures for the two SRM approaches, solar insolation reduction increases global average surface ozone concentrations, while sulfate injection decreases it. A fundamental difference between the two geoengineering schemes is the importance of heterogeneous reactions in the photochemical ozone balance with larger stratospheric sulfate abundance, resulting in increased ozone depletion in mid- and high latitudes. This reduces the net transport of stratospheric ozone into the troposphere and thus is a key driver of the overall decrease in surface ozone. At the same time, the change in stratospheric ozone alters the tropospheric photochemical environment due to enhanced ultraviolet radiation. A shared factor among both SRM scenarios is decreased chemical ozone loss due to reduced tropospheric humidity. Under insolation reduction, this is the dominant factor giving rise to the global surface ozone increase. Regionally, both surface ozone increases and decreases are found for both scenarios; that is, SRM would affect regions of the world differently in terms of air

  9. Impacts of stratospheric sulfate geoengineering on tropospheric ozone

    Science.gov (United States)

    Xia, Lili; Nowack, Peer J.; Tilmes, Simone; Robock, Alan

    2017-10-01

    A range of solar radiation management (SRM) techniques has been proposed to counter anthropogenic climate change. Here, we examine the potential effects of stratospheric sulfate aerosols and solar insolation reduction on tropospheric ozone and ozone at Earth's surface. Ozone is a key air pollutant, which can produce respiratory diseases and crop damage. Using a version of the Community Earth System Model from the National Center for Atmospheric Research that includes comprehensive tropospheric and stratospheric chemistry, we model both stratospheric sulfur injection and solar irradiance reduction schemes, with the aim of achieving equal levels of surface cooling relative to the Representative Concentration Pathway 6.0 scenario. This allows us to compare the impacts of sulfate aerosols and solar dimming on atmospheric ozone concentrations. Despite nearly identical global mean surface temperatures for the two SRM approaches, solar insolation reduction increases global average surface ozone concentrations, while sulfate injection decreases it. A fundamental difference between the two geoengineering schemes is the importance of heterogeneous reactions in the photochemical ozone balance with larger stratospheric sulfate abundance, resulting in increased ozone depletion in mid- and high latitudes. This reduces the net transport of stratospheric ozone into the troposphere and thus is a key driver of the overall decrease in surface ozone. At the same time, the change in stratospheric ozone alters the tropospheric photochemical environment due to enhanced ultraviolet radiation. A shared factor among both SRM scenarios is decreased chemical ozone loss due to reduced tropospheric humidity. Under insolation reduction, this is the dominant factor giving rise to the global surface ozone increase. Regionally, both surface ozone increases and decreases are found for both scenarios; that is, SRM would affect regions of the world differently in terms of air pollution. In conclusion

  10. Coating and dispersion of ceramic nanoparticles by UV-ozone etching assisted surface-initiated living radical polymerization.

    Science.gov (United States)

    Arita, Toshihiko

    2010-10-01

    Commercially available unmodified ceramic nanoparticles (NPs) in dry powder state were surface-modified and dispersed in almost single-crystal size. The surface-initiated living radical polymerization after just UV-ozone soft etching enables one to graft polymers onto the surface of ceramic NPs and disperse them in solvents. Furthermore, a number of NPs were dispersed with single-crystal sizes. The technique developed here could be applied to almost all ceramic NPs including metal nitrides.

  11. Field-analysis of potable water quality and ozone efficiency in ozone-assisted biological filtration systems for surface water treatment.

    Science.gov (United States)

    Zanacic, Enisa; Stavrinides, John; McMartin, Dena W

    2016-11-01

    Potable water treatment in small communities is challenging due to a complexity of factors starting with generally poor raw water sources, a smaller tax and consumption base that limit capital and operating funds, and culminating in what is typically a less sophisticated and robust water treatment plant for production and delivery of safe, high quality potable water. The design and optimization of modular ozone-assisted biological filtration systems can address some of these challenges. In surface water treatment, the removal of organic matter (e.g., dissolved organic carbon - DOC), inorganic nutrients and other exposure-related contaminants (e.g., turbidity and dissolved solids) from the raw water source is essential. Thus, a combination of chemical and biological oxidation processes can produce an effective and efficient water treatment plant design that is also affordable and robust. To that end, the ozone-assisted biological filtration water treatment plants in two communities were evaluated to determine the efficacy of oxidation and contaminant removal processes. The results of testing for in-field system performance indicate that plant performance is particularly negatively impacted by high alkalinity, high organics loading, and turbidity. Both bicarbonate and carbonate alkalinity were observed to impede ozone contact and interaction with DOC, resulting in lower than anticipated DOC oxidation efficiency and bioavailability. The ozone dosage at both water treatment plants must be calculated on a more routine basis to better reflect both the raw water DOC concentration and presence of alkalinities to ensure maximized organics oxidation and minimization of trihalomethanes production. Copyright © 2016 The Authors. Published by Elsevier Ltd.. All rights reserved.

  12. Surface ozone at the Devils Postpile National Monument receptor site during low and high wildland fire years

    Science.gov (United States)

    Andrzej Bytnerowicz; Joel D. Burley; Ricardo Cisneros; Haiganoush K. Preisler; Susan Schilling; Donald Schweizer; John Ray; Deanna Dulen; Christopher Beck; Bianca Auble

    2013-01-01

    Surface ozone (O3) was measured at the Devils Postpile National Monument (DEPO), eastern Sierra Nevada Mountains, California, during the 2007 (low-fire) and 2008 (high-fire) summer seasons. While mean and median values of O3 concentrations for the 2007 and 2008 summer seasons were similar, maximum O3...

  13. Impacts of urban land-surface forcing on ozone air quality in the Seoul metropolitan area

    Directory of Open Access Journals (Sweden)

    Y.-H. Ryu

    2013-02-01

    Full Text Available Modified local meteorology owing to heterogeneities in the urban–rural surface can affect urban air quality. In this study, the impacts of urban land-surface forcing on ozone air quality during a high ozone (O3 episode in the Seoul metropolitan area, South Korea, are investigated using a high-resolution chemical transport model (CMAQ. Under fair weather conditions, the temperature excess (urban heat island significantly modifies boundary layer characteristics/structures and local circulations. The modified boundary layer and local circulations result in an increase in O3 levels in the urban area of 16 ppb in the nighttime and 13 ppb in the daytime. Enhanced turbulence in the deep urban boundary layer dilutes pollutants such as NOx, and this contributes to the elevated O3 levels through the reduced O3 destruction by NO in the NOx-rich environment. The advection of O3 precursors over the mountains near Seoul by the prevailing valley-breeze circulation in the mid- to late morning results in the build-up of O3 over the mountains in conjunction with biogenic volatile organic compound (BVOC emissions there. As the prevailing local circulation in the afternoon changes to urban-breeze circulation, the O3-rich air masses over the mountains are advected over the urban area. The urban-breeze circulation exerts significant influences on not only the advection of O3 but also the chemical production of O3 under the circumstances in which both anthropogenic and biogenic (natural emissions play important roles in O3 formation. As the air masses that are characterized by low NOx and high BVOC levels and long OH chain length are advected over the urban area from the surroundings, the ozone production efficiency increases in the urban area. The relatively strong vertical mixing in the urban boundary layer embedded in the

  14. Quantitative Hydrocarbon Surface Analysis

    Science.gov (United States)

    Douglas, Vonnie M.

    2000-01-01

    The elimination of ozone depleting substances, such as carbon tetrachloride, has resulted in the use of new analytical techniques for cleanliness verification and contamination sampling. The last remaining application at Rocketdyne which required a replacement technique was the quantitative analysis of hydrocarbons by infrared spectrometry. This application, which previously utilized carbon tetrachloride, was successfully modified using the SOC-400, a compact portable FTIR manufactured by Surface Optics Corporation. This instrument can quantitatively measure and identify hydrocarbons from solvent flush of hardware as well as directly analyze the surface of metallic components without the use of ozone depleting chemicals. Several sampling accessories are utilized to perform analysis for various applications.

  15. Depleted uranium

    International Nuclear Information System (INIS)

    Huffer, E.; Nifenecker, H.

    2001-02-01

    This document deals with the physical, chemical and radiological properties of the depleted uranium. What is the depleted uranium? Why do the military use depleted uranium and what are the risk for the health? (A.L.B.)

  16. Oxidative regeneration of toluene-saturated natural zeolite by gaseous ozone: The influence of zeolite chemical surface characteristics

    Energy Technology Data Exchange (ETDEWEB)

    Alejandro, Serguei [Laboratorio de Tecnologías Limpias (F. Ingeniería), Universidad Católica de la Santísima Concepción, Alonso de Ribera 2850, Concepción (Chile); Núcleo de Energías Renovables (F. Ingeniería), Universidad Católica de Temuco, Rudecindo Ortega 02950, Temuco (Chile); Valdés, Héctor, E-mail: hvaldes@ucsc.cl [Laboratorio de Tecnologías Limpias (F. Ingeniería), Universidad Católica de la Santísima Concepción, Alonso de Ribera 2850, Concepción (Chile); Manéro, Marie-Hélène [Université de Toulouse (France); INPT, UPS (France); Laboratoire de Génie Chimique, 4, Allée Emile Monso, F–31030 Toulouse (France); CNRS (France); Laboratoire de Génie Chimique, F–31030 Toulouse (France); Zaror, Claudio A. [Departamento de Ingeniería Química (F. Ingeniería), Universidad de Concepción, Concepción, Correo 3, Casilla 160–C (Chile)

    2014-06-01

    Highlights: • Surface acidity of modified natural zeolite is related to its chemical reactivity. • Brønsted acid sites are associated to toluene adsorption. • Lewis acid sites could decompose ozone generating surface active oxygen species. • Infrared spectra evidence active atomic oxygen and oxidation by-product formation. • 2NH4Z1 sample shows the highest reactivity toward adsorbed toluene. - Abstract: In this study, the effect of zeolite chemical surface characteristics on the oxidative regeneration of toluene saturated-zeolite samples is investigated. A Chilean natural zeolite (53% clinoptilolite, 40% mordenite and 7% quartz) was chemically modified by acid treatment with hydrochloric acid and by ion-exchange with ammonium sulphate. Thermal pre-treatments at 623 and 823 K were applied and six zeolite samples with different chemical surface characteristics were generated. Chemical modification of natural zeolite followed by thermal out-gassing allows distinguishing the role of acidic surface sites on the regeneration of exhausted zeolites. An increase in Brønsted acid sites on zeolite surface is observed as a result of ammonium-exchange treatment followed by thermal treatment at 623 K, thus increasing the adsorption capacity toward toluene. High ozone consumption could be associated to a high content of Lewis acid sites, since these could decompose ozone into atomic active oxygen species. Then, surface oxidation reactions could take part among adsorbed toluene at Brønsted acid sites and surface atomic oxygen species, reducing the amount of adsorbed toluene after the regenerative oxidation with ozone. Experimental results show that the presence of adsorbed oxidation by-products has a negative impact on the recovery of zeolite adsorption capacity.

  17. Oxidative regeneration of toluene-saturated natural zeolite by gaseous ozone: The influence of zeolite chemical surface characteristics

    International Nuclear Information System (INIS)

    Alejandro, Serguei; Valdés, Héctor; Manéro, Marie-Hélène; Zaror, Claudio A.

    2014-01-01

    Highlights: • Surface acidity of modified natural zeolite is related to its chemical reactivity. • Brønsted acid sites are associated to toluene adsorption. • Lewis acid sites could decompose ozone generating surface active oxygen species. • Infrared spectra evidence active atomic oxygen and oxidation by-product formation. • 2NH4Z1 sample shows the highest reactivity toward adsorbed toluene. - Abstract: In this study, the effect of zeolite chemical surface characteristics on the oxidative regeneration of toluene saturated-zeolite samples is investigated. A Chilean natural zeolite (53% clinoptilolite, 40% mordenite and 7% quartz) was chemically modified by acid treatment with hydrochloric acid and by ion-exchange with ammonium sulphate. Thermal pre-treatments at 623 and 823 K were applied and six zeolite samples with different chemical surface characteristics were generated. Chemical modification of natural zeolite followed by thermal out-gassing allows distinguishing the role of acidic surface sites on the regeneration of exhausted zeolites. An increase in Brønsted acid sites on zeolite surface is observed as a result of ammonium-exchange treatment followed by thermal treatment at 623 K, thus increasing the adsorption capacity toward toluene. High ozone consumption could be associated to a high content of Lewis acid sites, since these could decompose ozone into atomic active oxygen species. Then, surface oxidation reactions could take part among adsorbed toluene at Brønsted acid sites and surface atomic oxygen species, reducing the amount of adsorbed toluene after the regenerative oxidation with ozone. Experimental results show that the presence of adsorbed oxidation by-products has a negative impact on the recovery of zeolite adsorption capacity

  18. A simple UV-ozone surface treatment to enhance photocatalytic performance of TiO 2 loaded polymer nanofiber membranes

    KAUST Repository

    Dilpazir, S.

    2016-01-29

    Homogeneously dispersed titanium dioxide loaded polyacrylonitrile nanofiber membranes with increased active mass loading, Ti3+ surface defects and hydrophilicity were fabricated by combining electrospinning and UV-ozone surface treatment. The photocatalytic activity improved by a factor of ∼2 and the kinetics of photodegradation switched from pseudo-first order to pseudo-second order with increasing TiO2 content with a maximum rate constant of 20.7 h-1. © The Royal Society of Chemistry 2016.

  19. Oxygen termination of homoepitaxial diamond surface by ozone and chemical methods: An experimental and theoretical perspective

    Science.gov (United States)

    Navas, Javier; Araujo, Daniel; Piñero, José Carlos; Sánchez-Coronilla, Antonio; Blanco, Eduardo; Villar, Pilar; Alcántara, Rodrigo; Montserrat, Josep; Florentin, Matthieu; Eon, David; Pernot, Julien

    2018-03-01

    Phenomena related with the diamond surface of both power electronic and biosensor devices govern their global behaviour. In particular H- or O-terminations lead to wide variations in their characteristics. To study the origins of such aspects in greater depth, different methods to achieve oxygen terminated diamond were investigated following a multi-technique approach. DFT calculations were then performed to understand the different configurations between the C and O atoms. Three methods for O-terminating the diamond surface were performed: two physical methods with ozone at different pressures, and an acid chemical treatment. X-ray photoelectron spectroscopy, spectroscopic ellipsometry, HRTEM, and EELS were used to characterize the oxygenated surface. Periodic-DFT calculations were undertaken to understand the effect of the different ways in which the oxygen atoms are bonded to carbon atoms on the diamond surface. XPS results showed the presence of hydroxyl or ether groups, composed of simple Csbnd O bonds, and the acid treatment resulted in the highest amount of O on the diamond surface. In turn, ellipsometry showed that the different treatments led to the surface having different optical properties, such as a greater refraction index and extinction coefficient in the case of the sample subjected to acid treatment. TEM analysis showed that applying temperature treatment improved the distribution of the oxygen atoms at the interface and that this generates a thinner amount of oxygen at each position and higher interfacial coverage. Finally, DFT calculations showed both an increase in the number of preferential electron transport pathways when π bonds and ether groups appear in the system, and also the presence of states in the middle of the band gap when there are π bonds, Cdbnd C or Cdbnd O.

  20. Ultrahigh nanoparticle stability against salt, pH, and solvent with retained surface accessibility via depletion stabilization.

    Science.gov (United States)

    Zhang, Xu; Servos, Mark R; Liu, Juewen

    2012-06-20

    For many applications, it is desirable to stabilize colloids over a wide range of buffer conditions while still retaining surface accessibility for adsorption and reaction. Commonly used charge or steric stabilization cannot achieve this goal since the former is sensitive to salt and the latter blocks the particle surface. We use depletion stabilization in the presence of high molecular weight polyethylene glycol (PEG) to stabilize a diverse range of nanomaterials, including gold nanoparticles (from 10 to 100 nm), graphene oxide, quantum dots, silica nanoparticles, and liposomes in the presence of Mg(2+) (>1.6 M), heavy metal ions, extreme pH (pH 1-13), organic solvents, and adsorbed nucleosides and drugs. At the same time, the particle surface remains accessible for adsorption of both small molecules and macromolecules. Based on this study, high loading of thiolated DNA was achieved in one step with just 2% PEG 20,000 in 2 h.

  1. Characterization of ion distributions near the surface of sodium-containing and sodium-depleted calcium aluminosilicate glass melts

    International Nuclear Information System (INIS)

    Corrales, Louis R.; Du, Jincheng

    2006-01-01

    The distribution of cation and anion components of sodium containing calcium aluminosilicate glass was studied by classical molecular dynamics simulations in a high temperature melt in the bulk and at the vacuum-melt interface. A significant redistribution of the sodium and non-bridging oxygen ions was observed. Subsequently, a sodium depleted calcium aluminosilicate glass melt was simulated to determine the sensitivity of the redistribution of ions near the vacuum-melt interface to the presence of sodium ions. It is found that the thermodynamic equilibrium condition near a surface favors the enrichment of non-bridging oxygen ions that is closely associated with enrichment of the sodium ions

  2. Modeling and analysis of surface potential of single gate fully depleted SOI MOSFET using 2D-Poisson's equation

    Science.gov (United States)

    Mani, Prashant; Tyagi, Chandra Shekhar; Srivastav, Nishant

    2016-03-01

    In this paper the analytical solution of the 2D Poisson's equation for single gate Fully Depleted SOI (FDSOI) MOSFET's is derived by using a Green's function solution technique. The surface potential is calculated and the threshold voltage of the device is minimized for the low power consumption. Due to minimization of threshold voltage the short channel effect of device is suppressed and after observation we obtain the device is kink free. The structure and characteristics of SingleGate FDSOI MOSFET were matched by using MathCAD and silvaco respectively.

  3. Response of the global surface ozone distribution to Northern Hemisphere sea surface temperature changes: implications for long-range transport

    Science.gov (United States)

    Yi, Kan; Liu, Junfeng; Ban-Weiss, George; Zhang, Jiachen; Tao, Wei; Cheng, Yanli; Tao, Shu

    2017-07-01

    The response of surface ozone (O3) concentrations to basin-scale warming and cooling of Northern Hemisphere oceans is investigated using the Community Earth System Model (CESM). Idealized, spatially uniform sea surface temperature (SST) anomalies of ±1 °C are individually superimposed onto the North Pacific, North Atlantic, and North Indian oceans. Our simulations suggest large seasonal and regional variability in surface O3 in response to SST anomalies, especially in the boreal summer. The responses of surface O3 associated with basin-scale SST warming and cooling have similar magnitude but are opposite in sign. Increasing the SST by 1 °C in one of the oceans generally decreases the surface O3 concentrations from 1 to 5 ppbv. With fixed emissions, SST increases in a specific ocean basin in the Northern Hemisphere tend to increase the summertime surface O3 concentrations over upwind regions, accompanied by a widespread reduction over downwind continents. We implement the integrated process rate (IPR) analysis in CESM and find that meteorological O3 transport in response to SST changes is the key process causing surface O3 perturbations in most cases. During the boreal summer, basin-scale SST warming facilitates the vertical transport of O3 to the surface over upwind regions while significantly reducing the vertical transport over downwind continents. This process, as confirmed by tagged CO-like tracers, indicates a considerable suppression of intercontinental O3 transport due to increased tropospheric stability at lower midlatitudes induced by SST changes. Conversely, the responses of chemical O3 production to regional SST warming can exert positive effects on surface O3 levels over highly polluted continents, except South Asia, where intensified cloud loading in response to North Indian SST warming depresses both the surface air temperature and solar radiation, and thus photochemical O3 production. Our findings indicate a robust linkage between basin-scale SST

  4. Response of the global surface ozone distribution to Northern Hemisphere sea surface temperature changes: implications for long-range transport

    Directory of Open Access Journals (Sweden)

    K. Yi

    2017-07-01

    Full Text Available The response of surface ozone (O3 concentrations to basin-scale warming and cooling of Northern Hemisphere oceans is investigated using the Community Earth System Model (CESM. Idealized, spatially uniform sea surface temperature (SST anomalies of ±1 °C are individually superimposed onto the North Pacific, North Atlantic, and North Indian oceans. Our simulations suggest large seasonal and regional variability in surface O3 in response to SST anomalies, especially in the boreal summer. The responses of surface O3 associated with basin-scale SST warming and cooling have similar magnitude but are opposite in sign. Increasing the SST by 1 °C in one of the oceans generally decreases the surface O3 concentrations from 1 to 5 ppbv. With fixed emissions, SST increases in a specific ocean basin in the Northern Hemisphere tend to increase the summertime surface O3 concentrations over upwind regions, accompanied by a widespread reduction over downwind continents. We implement the integrated process rate (IPR analysis in CESM and find that meteorological O3 transport in response to SST changes is the key process causing surface O3 perturbations in most cases. During the boreal summer, basin-scale SST warming facilitates the vertical transport of O3 to the surface over upwind regions while significantly reducing the vertical transport over downwind continents. This process, as confirmed by tagged CO-like tracers, indicates a considerable suppression of intercontinental O3 transport due to increased tropospheric stability at lower midlatitudes induced by SST changes. Conversely, the responses of chemical O3 production to regional SST warming can exert positive effects on surface O3 levels over highly polluted continents, except South Asia, where intensified cloud loading in response to North Indian SST warming depresses both the surface air temperature and solar radiation, and thus photochemical O3 production. Our findings indicate a robust linkage

  5. Impact of Future Emissions and Climate Change on Surface Ozone over China

    Science.gov (United States)

    Ma, C. T.; Westervelt, D. M.; Fiore, A. M.; Rieder, H. E.; Kinney, P.; Wang, S.; Correa, G. J. P.

    2017-12-01

    China's immense ambient air pollution problem and world-leading greenhouse gas emissions place it at the forefront of global efforts to address these related environmental concerns. Here, we analyze the impact of ECLIPSE (Evaluating the Climate and Air Quality Impacts of Short-Lived Pollutants) future emissions scenarios representative of current legislation (CLE) and maximum technically feasible emissions reductions (MFR) on surface ozone (O3) concentrations over China in the 2030s and 2050s, in the context of a changing climate. We use a suite of simulations performed with the NOAA Geophysical Fluid Dynamics Laboratory's AM3 global chemistry-climate model. To estimate the impact of climate change in isolation on Chinese air quality, we hold emissions of air pollutants including O3 precursors fixed at 2015 levels but allow climate (global sea surface temperatures and sea ice cover) to change according to decadal averages for the years 2026-2035 and 2046-2055 from a three-member ensemble of GFDL-CM3 simulations under the RCP8.5 high warming scenario. Evaluation of the present-day simulation (2015 CLE) with observations from 1497 chiefly urban air quality monitoring stations shows that simulated surface O3 is positively biased by 26 ppb on average over the domain of China. Previous studies, however, have shown that the modeled ozone response to changes in NOx emissions over the Eastern United States mirrors the magnitude and structure of observed changes in maximum daily average 8-hour (MDA8) O3 distributions. Therefore, we use the model's simulated changes for the 2030s and 2050s to project changes in policy-relevant MDA8 O3 concentrations. We find an overall increase in MDA8 O3 for CLE scenarios in which emissions of NOx precursors are projected to increase, and under MFR scenarios, an overall decrease, with the highest changes occurring in summertime for both 2030 and 2050 MFR. Under climate change alone, the model simulates a mean summertime decrease of 1.3 ppb

  6. Observations of atmospheric ozone - 38 to 76 deg north latitude at altitudes from 8 km to the surface

    Science.gov (United States)

    Gregory, G. L.; Beck, S. M.; Hudgins, C. H.

    1984-01-01

    Ozone data were obtained from 8 km to the surface and at latitudes from 38 to 76 deg N during January and February 1983. Flight lines covered northeastern U.S., Canada, and Greenland. The results of the latitudinal survey at 5- to 8-km altitude showed O3 mixing ratios to be about 40 ppbv with little variation in latitude. One region of elevated O3 was observed and extended from 54 N to 57 deg N latitude. Ozone reached 150 ppbv at 6.4-km altitude. This sampling was stratospheric air as the tropopause height was 5.6-km altitude. Profiles at 76, 67, and 53 deg N showed O3 to be be well mixed from about 5 km to the surface. In some cases, profiles identified a layer of 1 km to 100 m vertical dimension at the surface, in which O3 destruction had occurred.

  7. Surface Ozone Measured at GLOBE Schools in the Czech Republic: A Demonstration of the Importance of Student Contribution to the Larger Science Picture

    Science.gov (United States)

    Pippin, Margaret R.; Creilson, John K.; Henderson, Bryana L.; Ladd, Irene H.; Fishman, Jack; Votapkova, Dana; Krpcova, Ilona

    2008-01-01

    GLOBE (Global Learning and Observations to Benefit the Environment) is a worldwide hands-on, primary and secondary school-based education and science program, developed to give students a chance to perform real science by making measurements, analyzing data, and participating in research in collaboration with scientists. As part of the GLOBE Surface Ozone Protocol and with the assistance of the TEREZA Association in the Czech Republic, schools in the Czech Republic have been making and reporting daily measurements of surface ozone and surface meteorological data since 2001. Using a hand-held ozone monitor developed for GLOBE, students at several Czech schools have generated multiyear data records of surface ozone from 2001 to 2005. Analysis of the data shows surface ozone levels were anomalously high during the summer of 2003 relative to other summers. These findings are consistent with measurements by the European Environment Agency that highlights the summer of 2003 as having exceptionally long-lasting and spatially extensive episodes of high surface ozone, especially during the first half of August. Further analysis of the summer s prevailing meteorology shows not only that it was one of the hottest on record, a finding also seen in the student data, but the conditions for production of ozone were ideal. Findings such as these increase student, teacher, and scientist confidence in the utility of the GLOBE data for engaging budding scientists in the collection, analysis, and eventual interpretation of the data for inquiry-based education.

  8. Factors Controlling Summertime Surface Ozone In The Western U.S

    Science.gov (United States)

    Gao, Mei

    In this dissertation we investigate different factors controlling summertime surface ozone (O3) in the western U.S., including the impacts from increased wildfire emissions, the modulation by North American summer monsoon as well as long-range transport of O3 and its precursors from outside of North America. We first analyze the surface ozone observations from the Clean Air Status and Trend Network (CASTNet) using a global chemical transport model (GEOS-Chem) to investigate the impact of biomass burning on surface O3 in the western U.S. (WUS) mountain ranges during the June--October fire season of 2007, one of the stronger fire years in the WUS in the past decade. GEOS-Chem O3 captures the observed seasonal, synoptic and daily variations. Model daily afternoon average surface O3 concentrations at the CASTNet sites are within 2 ppb of the observations, with correlation coefficients of 0.51--0.83 and Taylor scores of 0.64--0.92. Observed maximum daily 8-hour (MAD8) surface O3 concentrations are 37--8 ppb at the sites, while the corresponding model results are higher by 6 ppb on average. Model results show July--September maximum surface O3 enhancement of ~9 ppb on average because of biomass burning. Peaks in fire-contributed surface O3 correspond broadly with high levels of potassium (K), reaffirming a strong fire influence. We find a policy relevant background (PRB) O3 of 45.6 ppb on average during July--September. Fire-contributed O3 accounts for up to 30% of the PRB O3, highest in the intense fire region (Montana, Idaho, and Wyoming) with maxima in August and September. We also examine an unexpected summertime surface O3 minimum (~30--5 ppb) in July--August 2007 observed throughout the Southwestern U.S. (SWUS) by interpreting observations of O3 and rainfall from the Clean Air Status and Trends Network (CASTNet) with a global chemical transport model. The O3 minimum reflects competing chemical and dynamic factors as well as anthropogenic and natural influences. Its

  9. Spatio-temporal trends of surface ozone and its related factors in Shanghai

    Science.gov (United States)

    Lin, Y.; Duan, Y.; Fu, Q.; Wang, Q.; Hu, M.

    2017-12-01

    The monitoring data in Shanghai during 2006-2016 demonstrated that the ozone concentration is increasing annually, however, the interannual changing trend of the relevant meteorological factors is not significant except horizontal wind speed. The diurnal variation of O3 hourly concentration indicated that the duration of O3 pollution has been increased. The spatial analysis of ozone pollution found that the ozone exceedances in the southwest suburbs is more prominent than other areas, while the potential of increasing ozone exceedances can not be ignored in the downtown of Shanghai. Ozone pollution wind roses of multiple sites demostrated that the southern part of Shanghai is the key area that affects the ozone pollution in Shanghai. The analysis of the impact of NO2 emission reduction shows that although the annual concencentration of O3 at Shanghai is increasing, however, the inner ring area and North suburbs, where the NO2 emission reduction are the most obvious, the rising rate of ozone is much lower than the area between inner and outer ring and western suburbs. Therefore, the ozone pollution control in Shanghai should stick to the reduction of NOx, and simultaneously promote the reduction of VOCs.

  10. The response of surface ozone to climate change over the Eastern United States

    Directory of Open Access Journals (Sweden)

    P. N. Racherla

    2008-02-01

    Full Text Available We investigate the response of surface ozone (O3 to future climate change in the eastern United States by performing simulations corresponding to present (1990s and future (2050s climates using an integrated model of global climate, tropospheric gas-phase chemistry, and aerosols. A future climate has been imposed using ocean boundary conditions corresponding to the IPCC SRES A2 scenario for the 2050s decade. Present-day anthropogenic emissions and CO2/CH4 mixing ratios have been used in both simulations while climate-sensitive emissions were allowed to vary with the simulated climate. The severity and frequency of O3 episodes in the eastern U.S. increased due to future climate change, primarily as a result of increased O3 chemical production. The 95th percentile O3 mixing ratio increased by 5 ppbv and the largest frequency increase occured in the 80–90 ppbv range; the US EPA's current 8-h ozone primary standard is 80 ppbv. The increased O3 chemical production is due to increases in: 1 natural isoprene emissions; 2 hydroperoxy radical concentrations resulting from increased water vapor concentrations; and, 3 NOx concentrations resulting from reduced PAN. The most substantial and statistically significant (p<0.05 increases in episode frequency occurred over the southeast and midatlantic U.S., largely as a result of 20% higher annual-average natural isoprene emissions. These results suggest a lengthening of the O3 season over the eastern U.S. in a future climate to include late spring and early fall months. Increased chemical production and shorter average lifetime are two consistent features of the seasonal response of surface O3, with increased dry deposition loss rates contributing most to the reduced lifetime in all seasons except summer. Significant interannual variability is observed in the frequency of O3

  11. The effect of entrainment through atmospheric boundary layer growth on observed and modeled surface ozone in the Colorado Front Range

    Science.gov (United States)

    Kaser, L.; Patton, E. G.; Pfister, G. G.; Weinheimer, A. J.; Montzka, D. D.; Flocke, F.; Thompson, A. M.; Stauffer, R. M.; Halliday, H. S.

    2017-06-01

    Ozone concentrations at the Earth's surface are controlled by meteorological and chemical processes and are a function of advection, entrainment, deposition, and net chemical production/loss. The relative contributions of these processes vary in time and space. Understanding the relative importance of these processes controlling surface ozone concentrations is an essential component for designing effective regulatory strategies. Here we focus on the diurnal cycle of entrainment through atmospheric boundary layer (ABL) growth in the Colorado Front Range. Aircraft soundings and surface observations collected in July/August 2014 during the DISCOVER-AQ/FRAPPÉ (Deriving Information on Surface conditions from Column and Vertically Resolved Observations Relevant to Air Quality/Front Range Air Pollution and Photochemistry Éxperiment) campaigns and equivalent data simulated by a regional chemical transport model are analyzed. Entrainment through ABL growth is most important in the early morning, fumigating the surface at a rate of 5 ppbv/h. The fumigation effect weakens near noon and changes sign to become a small dilution effect in the afternoon on the order of -1 ppbv/h. The chemical transport model WRF-Chem (Weather Research and Forecasting Model with chemistry) underestimates ozone at all altitudes during this study on the order of 10-15 ppbv. The entrainment through ABL growth is overestimated by the model in the order of 0.6-0.8 ppbv/h. This results from differences in boundary layer growth in the morning and ozone concentration jump across the ABL top in the afternoon. This implicates stronger modeled fumigation in the morning and weaker modeled dilution after 11:00 LT.

  12. Reformulated and alternative fuels: modeled impacts on regional air quality with special emphasis on surface ozone concentration.

    Science.gov (United States)

    Schell, Benedikt; Ackermann, Ingmar J; Hass, Heinz

    2002-07-15

    The comprehensive European Air Pollution and Dispersion model system was used to estimate the impacts of the usage of reformulated and alternative fuels on regional air quality with special emphasis on surface ozone concentrations. A severe western European summer smog episode in July 1994 has been used as a reference, and the model predictions have been evaluated for this episode. A forecast simulation for the year 2005 (TREND) has been performed, including the future emission development based on the current legislation and technologies available. The results of the scenario TREND are used as a baseline for the other 2005 fuel scenarios, including fuel reformulation, fuel sulfur content, and compressed natural gas (CNG) as an alternative fuel. Compared to the year 1994, significant reductions in episode peak ozone concentrations and ozone grid hours are predicted for the TREND scenario. These reductions are even more pronounced within the investigated alternative and reformulated fuel scenarios. Especially, low sulfur fuels are appropriate for an immediate improvement in air quality, because they effect the emissions of the whole fleet. Furthermore, the simulation results indicate that the introduction of CNG vehicles would also enhance air quality with respect to ozone.

  13. Platelet adhesion and protein adsorption on silicone rubber surface by ozone-induced grafted polymerization with carboxybetaine monomer.

    Science.gov (United States)

    Zhou, Jun; Yuan, Jiang; Zang, Xiaopeng; Shen, Jian; Lin, Sicong

    2005-03-10

    Platelet adhesion and protein adsorption on the silicone rubber film grafted with N,N'-dimethyl-N-methacryloyloxyethyl-N-(2-carboxyethyl) ammonium (DMMCA) was studied. The grafting was carried out by means of ozone-induced method and was confirmed by ATR-FTIR and XPS investigations. The grafted films possessed relatively hydrophilic surface revealed by contact angle measurement. The blood compatibility of the grafted film was evaluated in vitro by platelet adhesion in platelet-rich plasma (PRP) and protein absorption in bovine fibrinogen (BFG) using silicone film as the reference. No substantial platelet adhesion was observed for the grafted films incubated in PRP for 60 and 180 min. The protein absorption was also significantly reduced after incubated in bovine fibrinogen for 60 min. Both the results indicated that the blood compatibility of silicone rubber was greatly improved by ozone-induced grafting of carboxybetaine zwitterionic polymer onto its surface.

  14. Long-term change in the source contribution to surface ozone over Japan

    Science.gov (United States)

    Nagashima, Tatsuya; Sudo, Kengo; Akimoto, Hajime; Kurokawa, Junichi; Ohara, Toshimasa

    2017-07-01

    The relative contributions of various source regions to the long-term (1980-2005) increasing trend in surface ozone (O3) over Japan were estimated by a series of tracer-tagging simulations using a global chemical transport model. The model simulated the observed increasing trend in surface O3, including its seasonal variation and geographical features, in Japan well and demonstrated the relative roles of different source regions in forming this trend. Most of the increasing trend in surface O3 over Japan ( ˜ 97 %) that was simulated was explained as the sum of trends in contributions of different regions to photochemical O3 production. The increasing trend in O3 produced in China accounted for 36 % of the total increasing trend and those in the other northeast Asian regions (the Korean Peninsula, coastal regions in East Asia, and Japan) each accounted for about 12-15 %. Furthermore, the contributions of O3 created in the entire free troposphere and in western, southern, and southeastern Asian regions also increased, and their increasing trends accounted for 16 and 7 % of the total trend, respectively. The impact of interannual variations in climate, in methane concentration, and in emission of O3 precursors from different source regions on the relative contributions of O3 created in each region estimated above was also investigated. The variation of climate and the increase in methane concentration together caused the increase of photochemical O3 production in several regions, and represented about 19 % of the total increasing trend in surface O3 over Japan. The increase in emission of O3 precursors in China caused an increase of photochemical O3 production not only in China itself but also in the other northeast Asian regions and accounted for about 46 % of the total increase in surface O3 over Japan. Similarly, the relative impact of O3 precursor emission changes in the Korean Peninsula and Japan were estimated as about 16 and 4 % of the total increasing trend

  15. Springtime high surface ozone events over the western United States: Quantifying the role of stratospheric intrusions

    Science.gov (United States)

    Fiore, A. M.; Lin, M.; Cooper, O. R.; Horowitz, L. W.; Naik, V.; Levy, H.; Langford, A. O.; Johnson, B. J.; Oltmans, S. J.; Senff, C. J.

    2011-12-01

    As the National Ambient Air Quality (NAAQS) standard for ozone (O_{3}) is lowered, it pushes closer to policy-relevant background levels (O_{3} concentrations that would exist in the absence of North American anthropogenic emissions), making attainment more difficult with local controls. We quantify the Asian and stratospheric components of this North American background, with a primary focus on the western United States. Prior work has identified this region as a hotspot for deep stratospheric intrusions in spring. We conduct global simulations at 200 km and 50 km horizontal resolution with the GFDL AM3 model, including a stratospheric O_{3} tracer and two sensitivity simulations with anthropogenic emissions from Asia and North America turned off. The model is evaluated with a suite of in situ and satellite measurements during the NOAA CalNex campaign (May-June 2010). The model reproduces the principle features in the observed surface to near tropopause distribution of O_{3} along the California coast, including its latitudinal variation and the development of regional high-O_{3} episodes. Four deep tropopause folds are diagnosed and we find that the remnants of these stratospheric intrusions are transported to the surface of Southern California and Western U.S. Rocky Mountains, contributing 10-30 ppbv positive anomalies relative to the simulated campaign mean stratospheric component in the model surface layer. We further examine the contribution of North American background, including its stratospheric and Asian components, to the entire distribution of observed MDA8 O_{3} at 12 high-elevation CASTNet sites in the Mountain West. We find that the stratospheric O_{3} tracer constitutes 50% of the North American background, and can enhance surface maximum daily 8-hour average (MDA8) O_{3} by 20 ppb when observed surface O_{3} is in the range of 60-80 ppbv. Our analysis highlights the potential for natural sources such as deep stratospheric intrusions to contribute

  16. Optimization of artificial neural network models through genetic algorithms for surface ozone concentration forecasting.

    Science.gov (United States)

    Pires, J C M; Gonçalves, B; Azevedo, F G; Carneiro, A P; Rego, N; Assembleia, A J B; Lima, J F B; Silva, P A; Alves, C; Martins, F G

    2012-09-01

    This study proposes three methodologies to define artificial neural network models through genetic algorithms (GAs) to predict the next-day hourly average surface ozone (O(3)) concentrations. GAs were applied to define the activation function in hidden layer and the number of hidden neurons. Two of the methodologies define threshold models, which assume that the behaviour of the dependent variable (O(3) concentrations) changes when it enters in a different regime (two and four regimes were considered in this study). The change from one regime to another depends on a specific value (threshold value) of an explanatory variable (threshold variable), which is also defined by GAs. The predictor variables were the hourly average concentrations of carbon monoxide (CO), nitrogen oxide, nitrogen dioxide (NO(2)), and O(3) (recorded in the previous day at an urban site with traffic influence) and also meteorological data (hourly averages of temperature, solar radiation, relative humidity and wind speed). The study was performed for the period from May to August 2004. Several models were achieved and only the best model of each methodology was analysed. In threshold models, the variables selected by GAs to define the O(3) regimes were temperature, CO and NO(2) concentrations, due to their importance in O(3) chemistry in an urban atmosphere. In the prediction of O(3) concentrations, the threshold model that considers two regimes was the one that fitted the data most efficiently.

  17. Characteristics of surface ozone and nitrogen oxides at urban, suburban and rural sites in Ningbo, China

    Science.gov (United States)

    Tong, Lei; Zhang, Huiling; Yu, Jie; He, Mengmeng; Xu, Nengbin; Zhang, Jingjing; Qian, Feizhong; Feng, Jiayong; Xiao, Hang

    2017-05-01

    Surface ozone (O3) is a harmful air pollutant that has attracted growing concern in China. In this study, the mixing ratios of O3 and nitrogen oxides (NOx) at three different sites (urban, suburban and rural) of Ningbo were continuously measured to investigate the spatiotemporal characteristics of O3 and its relationships with environmental variables. The diurnal O3 variations were characterized by afternoon maxima (38.7-53.1 ppb on annual average) and early morning minima (11.7-26.2 ppb) at all the three sites. Two seasonal peaks of O3 were observed in spring (April or May) and autumn (October) with minima being observed in winter (December). NOx levels showed generally opposite variations to that of O3 with diurnal and seasonal maxima occurring in morning/evening rush-hours and in winter, respectively. As to the inter-annual variations of air pollutants, generally decreasing and increasing trends were observed in NO and O3 levels, respectively, from 2012 to 2015 at both urban and suburban sites. O3 levels were positively correlated with temperature but negatively correlated with relative humidity and NOx levels. Significant differences in O3 levels were observed for different wind speeds and wind directions (p population and plant growth.

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

    Science.gov (United States)

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

    2014-02-01

    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.

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

    Science.gov (United States)

    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.

  20. Influence of ozone precursors and particulate matter on the variation of surface ozone at an urban site of Delhi, India

    Directory of Open Access Journals (Sweden)

    Ashima Sharma

    2016-03-01

    Full Text Available Continuous measurements of surface O3 and its precursors (NO, NO2, CO, CH4 and NMHCs at an urban site of Delhi, India during January 2012 to December 2013 are presented. In the present study, the annual average mixing ratios of surface O3, NO, NO2, CO, CH4 and NMHC were 30 ± 6 ppb, 24 ± 6 ppb, 15 ± 4 ppb, 1.5 ± 0.4 ppm, 2.4 ± 0.4 ppm and 0.4 ± 0.1 ppm, respectively. The maximum average mixing ratios of surface O3, NO and NO2 were observed during the summer, whereas, the minimum average mixing ratios of ambient NO and NO2 were during monsoon seasons. The surface O3, NO and NO2 have shown the prominent diurnal variations during all the seasons at the observational site of Delhi. The result reveals that the surface O3 was negatively correlated with NOx and CO during the study. The linear scatter plot analysis shows that the PM2.5 and PM10 present in the ambient air of Delhi influence the production of surface O3 at observational site.

  1. Stratospheric solar geoengineering without ozone loss

    Science.gov (United States)

    Keith, David W.; Weisenstein, Debra K.; Dykema, John A.; Keutsch, Frank N.

    2016-12-01

    Injecting sulfate aerosol into the stratosphere, the most frequently analyzed proposal for solar geoengineering, may reduce some climate risks, but it would also entail new risks, including ozone loss and heating of the lower tropical stratosphere, which, in turn, would increase water vapor concentration causing additional ozone loss and surface warming. We propose a method for stratospheric aerosol climate modification that uses a solid aerosol composed of alkaline metal salts that will convert hydrogen halides and nitric and sulfuric acids into stable salts to enable stratospheric geoengineering while reducing or reversing ozone depletion. Rather than minimizing reactive effects by reducing surface area using high refractive index materials, this method tailors the chemical reactivity. Specifically, we calculate that injection of calcite (CaCO3) aerosol particles might reduce net radiative forcing while simultaneously increasing column ozone toward its preanthropogenic baseline. A radiative forcing of -1 Wṡm-2, for example, might be achieved with a simultaneous 3.8% increase in column ozone using 2.1 Tgṡy-1 of 275-nm radius calcite aerosol. Moreover, the radiative heating of the lower stratosphere would be roughly 10-fold less than if that same radiative forcing had been produced using sulfate aerosol. Although solar geoengineering cannot substitute for emissions cuts, it may supplement them by reducing some of the risks of climate change. Further research on this and similar methods could lead to reductions in risks and improved efficacy of solar geoengineering methods.

  2. Areal Measurements of Ozone, Water, and Heat Fluxes Over Land With Different Surface Complexity, Using Aircraft

    International Nuclear Information System (INIS)

    Hicks, Bruce B.

    2001-01-01

    Contemporary models addressing issues of air quality and/or atmospheric deposition continue to exploit air-surface exchange formulations originating from single-tower studies. In reality,these expressions describe situations that are rare in the real world - nearly flat and spatially homogeneous. There have been several theoretical suggestions about how to extend from single-point understanding to areal descriptions, but so far the capability to address the problem experimentally has been limited. In recent years, however, developments in sensing technology have permitted adaptation of eddy-correlation methods to low-flying aircraft in a far more cost-effective manner than previously. A series of field experiments has been conducted, ranging from flat farmland to rolling countryside, employing a recently modified research aircraft operated by the US NationalOceanic and Atmospheric Administration (NOAA). The results demonstrate the complexity of the spatial heterogeneity question,especially for pollutants (ozone in particular). In general, the uncertainty associated with the adoption of any single-point formulation when describing areal averages is likely to be in the range 10% to 40%. In the case of sensible and latent heat fluxes, the overall behavior is controlled by the amount of energy available. For pollutant deposition, there is no constraint equivalent to the net radiation limitation on convective heat exchange. Consequently, dry deposition rates and air-surface exchange of trace gases in general are especially vulnerable to errors in spatial extrapolation. The results indicate that the susceptibility of dry deposition formulations to terrain complexity depends on the deposition velocity itself. For readily transferred pollutants (such as HNO 3 ), a factor of two error could be involved

  3. Oxygen Depletion on the Surface of Mercury: Evidence of Silicon Smelting?

    Science.gov (United States)

    McCubbin, F. M.; Vander Kaaden, K. E.; Peplowski, P. N.; Bell, A. S.; Evans, L. G.; Nittler, L. R.; Boyce, J. W.; Keller, L. P.; McCoy, T. J.

    2017-01-01

    The MErcury Surface, Space ENvironment, GEochemistry, and Ranging (MESSENGER) spacecraft collected data that provided important insights into the structure, chemical makeup, and compositional diversity of Mercury. The X-Ray Spectrometer (XRS) and Gamma-Ray Spectrometer (GRS) onboard MESSENGER provided the first detailed chemical analyses of Mercury's surface. Among the many discoveries included several surprising characteristics about the surface of Mercury, including elevated S abundances (up to 4 percent by weight), low Fe abundances (less than 4 percent by weight), and relatively low O abundances (O/Si ratio of 1.40 plus or minus 0.03). The surface chemistry as determined by MESSENGER has been used to identify up to nine distinct geochemical terranes on Mercury. Numerous modeling and experimental efforts have been undertaken to infer the mineralogy and petrology of mercurian lavas and surface materials. However, all of these efforts have presumed valence states for each of the elements according to the following: Si4+, Ti4+, Al3+, Cr2+, Fe2+, Mn2+, Mg2+, Ca2+, Na+, K+, S2-, Cl-. Based on these valence assignments, cations are charged balanced with the anions O2-, S2-, and Cl- and the compositions are recast in terms of oxides, sulfides, and chlorides. Based on these assumptions, the geochemical terranes that have been identified on Mercury yield O/Si wt. ratios ranging from 1.61 to 1.84, which is substantially higher than the preliminary O/Si ratio of 1.40 plus or minus 0.03 determined by the MESSENGER GRS]. We have re-evaluated the O/Si ratio using the entire MESSENGER dataset to reassess its implications for the geochemistry of Mercury.

  4. Climate and emission changes contributing to changes in near-surface ozone in Europe over the coming decades: results from model studies.

    Science.gov (United States)

    Engardt, Magnuz; Bergström, Robert; Andersson, Camilla

    2009-12-01

    We used an off-line, regional, model of atmospheric transport and chemistry to investigate current and future levels of near-surface ozone and accumulated ozone exposure over a threshold of 40 ppb(v) (AOT40) in Europe. To describe the current situation and enable an evaluation of the model's performance we simulated a number of years around 2000. To assess changes in ozone concentrations due to possible emission changes in Europe, the model was run with the meteorology of the early 2000s and precursor emissions from a set of Clean Air for Europe (CAFE) emissions scenarios. By extrapolation of the observed increase in near-surface O3 at coastal locations in northwest Europe we constructed model boundaries that were used to simulate the impact of increasing hemispheric background in 2020. To assess changes in ozone concentrations due to climate change, the model was run with recent (2000) emissions but using meteorology from a regional climate model simulating a control (1961-1990) and a future (2021-2050) climate. The results indicate that climate change will have a small impact on ozone concentrations and AOT40 in the Nordic countries. Changes in hemispheric background concentrations and changes in precursor emissions in Europe will have a larger effect on ozone in Northern Europe. The situation is quite different in southern Europe, where climate change is expected to result in a very large increase in near-surface ozone concentrations.

  5. Impact of near-surface atmospheric composition on ozone formation in Russia

    Science.gov (United States)

    Berezina, Elena; Moiseenko, Konstantin; Skorokhod, Andrey; Belikov, Igor; Pankratova, Natalia; Elansky, Nikolai

    2017-04-01

    One of the consequences of the human impact on the atmosphere is increasing in tropospheric ozone concentration, with the highest ozone level being observed in industrially developed and highly populated regions of the world. In these regions, main anthropogenic sources of carbon monoxide (CO), methane (CH4) and volatile organic compounds (VOCs) are concentrated. The oxidation of these compounds, when interacting with hydroxyl and nitrogen oxides at rather high temperature and sunlight, leads to ozone formation. CO and CH4 are slowly oxidized in the atmosphere and cause an increase in global and regional background ozone. However, the oxidation of some VOCs occurs during daylight hours and is accompanied by an increase in ozone concentration near VOCs sources, particularly in urban and industrial areas. The contribution of biogenic VOCs to ozone generation is estimated to be from 40 to 70% of the total contribution of all chemical ozone precursors in the troposphere [1], with isoprene playing the main role in ozone formation [2]. The impact of aromatic hydrocarbons to ozone formation is reported to be about 40% of the total ozone generation from the oxidation of anthropogenic VOCs [3]. In this study, the results of VOCs measurements (isoprene, benzene, toluene, phenol, styrene, xylene and propilbenzene) by proton mass spectrometry in different regions of Russia along the Trans-Siberian railway from Moscow to Vladivostok from TROICA-12 campaign on a mobile laboratory in summer 2008 are analyzed. It is shown that the TROICA-12 measurements were carried out mostly in moderately polluted (2≤NOx20 ppb) conditions ( 20 and 2% of measurements, correspondingly). The lower troposphere chemical regime in the campaign is found to be mainly NOx sensitive, both in rural and urban environments, with typical morning NMHC/NOx ratios being well above 20. Hence, ozone production rates are expected to be controlled by regional NOx emissions and their complex interplay with both

  6. WRF-Chem simulated surface ozone over south Asia during the pre-monsoon: effects of emission inventories and chemical mechanisms

    Directory of Open Access Journals (Sweden)

    A. Sharma

    2017-12-01

    Full Text Available We evaluate numerical simulations of surface ozone mixing ratios over the south Asian region during the pre-monsoon season, employing three different emission inventories in the Weather Research and Forecasting model with Chemistry (WRF-Chem with the second-generation Regional Acid Deposition Model (RADM2 chemical mechanism: the Emissions Database for Global Atmospheric Research – Hemispheric Transport of Air Pollution (EDGAR-HTAP, the Intercontinental Chemical Transport Experiment phase B (INTEX-B and the Southeast Asia Composition, Cloud, Climate Coupling Regional Study (SEAC4RS. Evaluation of diurnal variability in modelled ozone compared to observational data from 15 monitoring stations across south Asia shows the model ability to reproduce the clean, rural and polluted urban conditions over this region. In contrast to the diurnal average, the modelled ozone mixing ratios during noontime, i.e. hours of intense photochemistry (11:30–16:30 IST – Indian Standard Time – UTC +5:30, are found to differ among the three inventories. This suggests that evaluations of the modelled ozone limited to 24 h average are insufficient to assess uncertainties associated with ozone buildup. HTAP generally shows 10–30 ppbv higher noontime ozone mixing ratios than SEAC4RS and INTEX-B, especially over the north-west Indo-Gangetic Plain (IGP, central India and southern India. The HTAP simulation repeated with the alternative Model for Ozone and Related Chemical Tracers (MOZART chemical mechanism showed even more strongly enhanced surface ozone mixing ratios due to vertical mixing of enhanced ozone that has been produced aloft. Our study indicates the need to also evaluate the O3 precursors across a network of stations and the development of high-resolution regional inventories for the anthropogenic emissions over south Asia accounting for year-to-year changes to further reduce uncertainties in modelled ozone over this region.

  7. WRF-Chem simulated surface ozone over south Asia during the pre-monsoon: effects of emission inventories and chemical mechanisms

    Science.gov (United States)

    Sharma, Amit; Ojha, Narendra; Pozzer, Andrea; Mar, Kathleen A.; Beig, Gufran; Lelieveld, Jos; Gunthe, Sachin S.

    2017-12-01

    We evaluate numerical simulations of surface ozone mixing ratios over the south Asian region during the pre-monsoon season, employing three different emission inventories in the Weather Research and Forecasting model with Chemistry (WRF-Chem) with the second-generation Regional Acid Deposition Model (RADM2) chemical mechanism: the Emissions Database for Global Atmospheric Research - Hemispheric Transport of Air Pollution (EDGAR-HTAP), the Intercontinental Chemical Transport Experiment phase B (INTEX-B) and the Southeast Asia Composition, Cloud, Climate Coupling Regional Study (SEAC4RS). Evaluation of diurnal variability in modelled ozone compared to observational data from 15 monitoring stations across south Asia shows the model ability to reproduce the clean, rural and polluted urban conditions over this region. In contrast to the diurnal average, the modelled ozone mixing ratios during noontime, i.e. hours of intense photochemistry (11:30-16:30 IST - Indian Standard Time - UTC +5:30), are found to differ among the three inventories. This suggests that evaluations of the modelled ozone limited to 24 h average are insufficient to assess uncertainties associated with ozone buildup. HTAP generally shows 10-30 ppbv higher noontime ozone mixing ratios than SEAC4RS and INTEX-B, especially over the north-west Indo-Gangetic Plain (IGP), central India and southern India. The HTAP simulation repeated with the alternative Model for Ozone and Related Chemical Tracers (MOZART) chemical mechanism showed even more strongly enhanced surface ozone mixing ratios due to vertical mixing of enhanced ozone that has been produced aloft. Our study indicates the need to also evaluate the O3 precursors across a network of stations and the development of high-resolution regional inventories for the anthropogenic emissions over south Asia accounting for year-to-year changes to further reduce uncertainties in modelled ozone over this region.

  8. The ozone backlash

    International Nuclear Information System (INIS)

    Taubes, G.

    1993-01-01

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

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

    Science.gov (United States)

    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.

  10. Surface ozone scenario and air quality in the north-central part of India.

    Science.gov (United States)

    Saini, Renuka; Taneja, Ajay; Singh, Pradyumn

    2017-09-01

    Tropospheric pollutants including surface ozone (O 3 ), nitrogen dioxide (NO 2 ), carbon monoxide (CO) and meteorological parameters were measured at a traffic junction (78°2' E and 27°11' N) in Agra, India from January 2012 to December 2012. Temporal analysis of pollutants suggests that annual average mixing ratios of tropospheric pollutants were: O 3 - 22.97±23.36ppbV, NO 2 - 19.84±16.71ppbV and CO - 0.91±0.86ppmV, with seasonal variations of O 3 having maximum mixing ratio during summer season (32.41±19.31ppbV), whereas lowest was found in post-monsoon season (8.74±3.8ppbV). O 3 precursors: NO 2 and CO, showed inverse relationship with O 3 . Seasonal variation and high O 3 episodes during summer are associated with meteorological parameters such as high solar radiation, atmospheric temperature and transboundary transport. The interdependence of these variables showed a link between the daytime mixing ratios of O 3 with the nighttime level of NO 2 . The mixing ratios of CO and NO 2 showed tight correlations, which confirms the influence of vehicular emissions combined with other anthropogenic activities due to office/working hours, shallowing, and widening of boundary layer. FLEXTRA backward trajectories for the O 3 episode days clearly indicate the transport from the NW and W to S/SE and SW direction at Agra in different seasons. Copyright © 2017. Published by Elsevier B.V.

  11. Detecting recovery of the stratospheric ozone layer

    Science.gov (United States)

    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.

  12. Inter-annual variability of surface ozone at coastal (Dumont d'Urville, 2004–2014 and inland (Concordia, 2007–2014 sites in East Antarctica

    Directory of Open Access Journals (Sweden)

    M. Legrand

    2016-07-01

    Full Text Available Surface ozone has been measured since 2004 at the coastal East Antarctic site of Dumont d'Urville (DDU, and since 2007 at the Concordia station located on the high East Antarctic plateau. This paper discusses long-term changes, seasonal and diurnal cycles, as well as inter-annual summer variability observed at these two East Antarctic sites. At Concordia, near-surface ozone data were complemented by balloon soundings and compared to similar measurements done at the South Pole. The DDU record is compared to those obtained at the coastal site of Syowa, also located in East Antarctica, as well as the coastal sites of Neumayer and Halley, both located on the coast of the Weddell Sea in West Antarctica. Surface ozone mixing ratios exhibit very similar seasonal cycles at Concordia and the South Pole. However, in summer the diurnal cycle of ozone is different at the two sites with a drop of ozone in the afternoon at Concordia but not at the South Pole. The vertical distribution of ozone above the snow surface also differs. When present, the ozone-rich layer located near the ground is better mixed and deeper at Concordia (up to 400 m than at the South Pole during sunlight hours. These differences are related to different solar radiation and wind regimes encountered at these two inland sites. DDU appears to be the coastal site where the impact of the late winter/spring bromine chemistry is the weakest, but where the impact of elevated ozone levels caused by NOx snow emissions from the high Antarctic plateau is the highest. The highest impact of the bromine chemistry is seen at Halley and Neumayer, and to a lesser extent at Syowa. These three sites are only weakly impacted by the NOx chemistry and the net ozone production occurring on the high Antarctic plateau. The differences in late winter/spring are attributed to the abundance of sea ice offshore from the sites, whereas those in summer are related to the topography of East Antarctica that promotes

  13. Surface ozone in the Southern Hemisphere: 20 years of data from a site with a unique setting in El Tololo, Chile

    Science.gov (United States)

    Anet, Julien G.; Steinbacher, Martin; Gallardo, Laura; Velásquez Álvarez, Patricio A.; Emmenegger, Lukas; Buchmann, Brigitte

    2017-05-01

    The knowledge of surface ozone mole fractions and their global distribution is of utmost importance due to the impact of ozone on human health and ecosystems and the central role of ozone in controlling the oxidation capacity of the troposphere. The availability of long-term ozone records is far better in the Northern than in the Southern Hemisphere, and recent analyses of the seven accessible records in the Southern Hemisphere have shown inconclusive trends. Since late 1995, surface ozone is measured in situ at "El Tololo", a high-altitude (2200 m a.s.l.) and pristine station in Chile (30° S, 71° W). The dataset has been recently fully quality controlled and reprocessed. This study presents the observed ozone trends and annual cycles and identifies key processes driving these patterns. From 1995 to 2010, an overall positive trend of ˜ 0.7 ppb decade-1 is found. Strongest trends per season are observed in March and April. Highest mole fractions are observed in late spring (October) and show a strong correlation with ozone transported from the stratosphere down into the troposphere, as simulated with a model. Over the 20 years of observations, the springtime ozone maximum has shifted to earlier times in the year, which, again, is strongly correlated with a temporal shift in the occurrence of the maximum of simulated stratospheric ozone transport at the site. We conclude that background ozone at El Tololo is mainly driven by stratospheric intrusions rather than photochemical production from anthropogenic and biogenic precursors. The major footprint of the sampled air masses is located over the Pacific Ocean. Therefore, due to the negligible influence of local processes, the ozone record also allows studying the influence of El Niño and La Niña episodes on background ozone levels in South America. In agreement with previous studies, we find that, during La Niña conditions, ozone mole fractions reach higher levels than during El Niño conditions.

  14. Exploring the direct impacts of particulate matter and surface ozone on global crop production

    Science.gov (United States)

    Schiferl, L. D.; Heald, C. L.

    2016-12-01

    The current era of rising food demand to feed an increasing population along with expansion of industrialization throughout the globe has been accompanied by deteriorating air quality and an enhancement in agricultural activity. Both air quality and the food supply are vitally important to sustaining human enterprise, and understanding the effects air quality may have on agricultural production is critical. Particulate matter (PM) in the atmosphere decreases the total photosynthetically available radiation (PAR) available to crops through the scattering and absorption of radiation while also increasing the diffuse fraction (DF) of this PAR. Since plants respond positively to a higher DF through the more even distribution of photons to all leaves, the net effect of PM on crop production depends on the magnitudes of these values and the response mechanisms of a specific crop. In contrast, atmospheric ozone always acts to decrease crop production through its phytotoxic properties. While the relationships between ozone and crop production have been readily studied, the effects of PM on crop production and their relative importance compared to ozone is much more uncertain. This study uses the GEOS-Chem chemical transport model linked to the RRTMG radiative transfer model and the DSSAT crop model to explore the impacts of PM and ozone on the globally distributed production of maize, rice, wheat and soybeans. First, we examine how air quality differentially affects total seasonal production by crop and region. Second, we investigate the dependence of simulated production on air quality over different timescales and under varying cloud conditions.

  15. Characteristics of Surface Ozone in Agra, a Sub-urban site in Indo ...

    Indian Academy of Sciences (India)

    65

    (2003) conducted their study at the high altitude site of Mt. ..... 247 other sites in India, ozone followed different diurnal and seasonal variations. At the high altitude. 248 site in Nainital (Sarangi et al., 2014), highest monthly mean (62 ..... meteorology on temporal evolution of O3 at a tropical location in northeast India; Environ.

  16. Characteristics of Surface Ozone in Agra, a Sub-urban site in Indo ...

    Indian Academy of Sciences (India)

    65

    Ozone (O3) is a secondary pollutant which has an important effect on air quality, climate. 49 change and atmospheric chemistry (Solomon et al., 2000; Sitch et al., 2007). Depending on its. 50 location in the atmosphere, O3 can influence human health and climate; in the stratosphere, O3. 51 filters out detrimental ultraviolet ...

  17. Climate-chemistry interaction affecting tropospheric ozone

    Science.gov (United States)

    Mao, Huiting

    1999-09-01

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

  18. Long-term trends of surface ozone and its influencing factors at the Mt Waliguan GAW station, China - Part 2: The roles of anthropogenic emissions and climate variability

    Science.gov (United States)

    Xu, Wanyun; Xu, Xiaobin; Lin, Meiyun; Lin, Weili; Tarasick, David; Tang, Jie; Ma, Jianzhong; Zheng, Xiangdong

    2018-01-01

    despite ozone increases in eastern China. Analysis of the Trajectory-mapped Ozonesonde data set for the Stratosphere and Troposphere (TOST) and trajectory residence time reveals increases in direct ozone transport from the eastern sector during autumn, which adds to the autumnal ozone increase. We further examine the links of ozone variability at WLG to the quasi-biennial oscillation (QBO), the East Asian summer monsoon (EASM), and the sunspot cycle. Our results suggest that the 2-3-, 3-7-, and 11-year periodicities are linked to the QBO, EASM index, and sunspot cycle, respectively. A multivariate regression analysis is performed to quantify the relative contributions of various factors to surface ozone concentrations at WLG. Through an observational and modelling analysis, this study demonstrates the complex relationships between surface ozone at remote locations and its dynamical and chemical influencing factors.

  19. Ozone Layer Educator's Guide.

    Science.gov (United States)

    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…

  20. Our Shrinking Ozone Layer

    Indian Academy of Sciences (India)

    Depletion of the Earth's ozone layer is one of the major environmental concerns for the new millennium having serious implications on human health, agriculture and cli- mate. In the past decades, research by the international scientific community has been directed towards under- standing the impact of human interference ...

  1. Application of Response Surface Methodology for characterization of ozone production from Multi-Cylinder Reactor in non-thermal plasma device

    Science.gov (United States)

    Lian See, Tan; Zulazlan Shah Zulkifli, Ahmad; Mook Tzeng, Lim

    2018-04-01

    Ozone is a reactant which can be applied for various environmental treatment processes. It can be generated via atmospheric air non-thermal plasmas when sufficient voltages are applied through a combination of electrodes and dielectric materials. In this study, the concentration of ozone generated via two different configurations of multi-cylinder dielectric barrier discharge (DBD) reactor (3 x 40 mm and 10 x 10 mm) was investigated. The influence of the voltage and the duty cycle to the concentration of ozone generated by each configuration was analysed using response surface methodology. Voltage was identified as significant factor to the ozone production process. However, the regressed model was biased towards one of the configuration, leaving the predicted results of another configuration to be out of range.

  2. Ozonation of Canadian Athabasca asphaltene

    Science.gov (United States)

    Cha, Zhixiong

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

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

    Science.gov (United States)

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

    2014-12-01

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

  4. Electron beam induced Hg desorption and the electronic structure of the Hg depleted surface of Hg1/sub -//sub x/Cd/sub x/Te

    International Nuclear Information System (INIS)

    Shih, C.K.; Friedman, D.J.; Bertness, K.A.; Lindau, I.; Spicer, W.E.; Wilson, J.A.

    1986-01-01

    Auger electron spectroscopy (AES), x-ray photoemission spectroscopy (XPS), low energy electron diffraction (LEED), and angle-resolved ultraviolet photoemission spectroscopy (ARPES) were used to study the electron beam induced Hg desorption from a cleaved (110)Hg/sub 1-//sub x/Cd/sub x/Te surface and the electronic structure of the Hg depleted surface. Solid state recrystallized Hg/sub 1-//sub x/Cd/sub x/Te single crystals were used. It was found that the electron beam heating dominated the electron beam induced Hg desorption on Hg/sub 1-//sub x/Cd/sub x/Te. At the electron beam energy used, the electron beam heating extended several thousand angstroms deep. However, the Hg depletion saturated after a few monolayers were depleted of Hg atoms. At the initial stage of Hg loss (only 3%), the surface band bends upward (more p type). The ARPES spectrum showed the loss of some E vs k dispersion after 22% Hg atoms were removed from the surface region, and no dispersion was observed after 43% Hg atoms were removed. These results have important implications on the electronic structure of the surfaces and interfaces of which the stoichiometry is altered

  5. Comment on "Cosmic-ray-driven reaction and greenhouse effect of halogenated molecules: Culprits for atmospheric ozone depletion and global climate change"

    Science.gov (United States)

    Nuccitelli, Dana; Cowtan, Kevin; Jacobs, Peter; Richardson, Mark; Way, Robert G.; Blackburn, Anne-Marie; Stolpe, Martin B.; Cook, John

    2014-04-01

    Lu (2013) (L13) argued that solar effects and anthropogenic halogenated gases can explain most of the observed warming of global mean surface air temperatures since 1850, with virtually no contribution from atmospheric carbon dioxide (CO2) concentrations. Here we show that this conclusion is based on assumptions about the saturation of the CO2-induced greenhouse effect that have been experimentally falsified. L13 also confuses equilibrium and transient response, and relies on data sources that have been superseeded due to known inaccuracies. Furthermore, the statistical approach of sequential linear regression artificially shifts variance onto the first predictor. L13's artificial choice of regression order and neglect of other relevant data is the fundamental cause of the incorrect main conclusion. Consideration of more modern data and a more parsimonious multiple regression model leads to contradiction with L13's statistical results. Finally, the correlation arguments in L13 are falsified by considering either the more appropriate metric of global heat accumulation, or data on longer timescales.

  6. Tropospheric ozone seasonal and long-term variability as seen by lidar and surface measurements at the JPL-Table Mountain Facility, California

    Directory of Open Access Journals (Sweden)

    M. J. Granados-Muñoz

    2016-07-01

    Full Text Available A combined surface and tropospheric ozone climatology and interannual variability study was performed for the first time using co-located ozone photometer measurements (2013–2015 and tropospheric ozone differential absorption lidar measurements (2000–2015 at the Jet Propulsion Laboratory Table Mountain Facility (TMF; elev. 2285 m, in California. The surface time series were investigated both in terms of seasonal and diurnal variability. The observed surface ozone is typical of high-elevation remote sites, with small amplitude of the seasonal and diurnal cycles, and high ozone values, compared to neighboring lower altitude stations representative of urban boundary layer conditions. The ozone mixing ratio ranges from 45 ppbv in the winter morning hours to 65 ppbv in the spring and summer afternoon hours. At the time of the lidar measurements (early night, the seasonal cycle observed at the surface is similar to that observed by lidar between 3.5 and 9 km. Above 9 km, the local tropopause height variation with time and season impacts significantly the ozone lidar observations. The frequent tropopause folds found in the vicinity of TMF (27 % of the time, mostly in winter and spring produce a dual-peak vertical structure in ozone within the fold layer, characterized by higher-than-average values in the bottom half of the fold (12–14 km, and lower-than-averaged values in the top half of the fold (14–18 km. This structure is consistent with the expected origin of the air parcels within the fold, i.e., mid-latitude stratospheric air folding down below the upper tropospheric sub-tropical air. The influence of the tropopause folds extends down to 5 km, increasing the ozone content in the troposphere. No significant signature of interannual variability could be observed on the 2000–2015 de-seasonalized lidar time series, with only a statistically non-significant positive anomaly during the years 2003–2007. Our trend analysis

  7. Effect of reactive surface area of minerals on mineralization and carbon dioxide trapping in a depleted gas reservoir

    NARCIS (Netherlands)

    Bolourinejad, P.; Shoeibi Omrani, P.; Herber, R.

    2014-01-01

    In this study, a long-term (up to 1000 years) geochemical modelling of subsurface CO2 storage was carried out on sandstone reservoirs of depleted gas fields in northeast Netherlands. It was found that mineral dissolution/precipitation has only a minor effect on reservoir porosity. In order to

  8. Effect of reactive surface area of minerals on mineralization and carbon dioxide trapping in a depleted gas reservoir

    NARCIS (Netherlands)

    Bolourinejad, Panteha; Omrani, Pejman Shoeibi; Herber, Rien

    In this study, a long-term (up to 1000 years) geochemical modelling of subsurface CO2 storage was carried out on sandstone reservoirs of depleted gas fields in northeast Netherlands. It was found that mineral dissolution/precipitation has only a minor effect on reservoir porosity. In order to

  9. Observed and predicted sensitivities of extreme surface ozone to meteorological drivers in three US cities

    Science.gov (United States)

    Fix, Miranda J.; Cooley, Daniel; Hodzic, Alma; Gilleland, Eric; Russell, Brook T.; Porter, William C.; Pfister, Gabriele G.

    2018-03-01

    We conduct a case study of observed and simulated maximum daily 8-h average (MDA8) ozone (O3) in three US cities for summers during 1996-2005. The purpose of this study is to evaluate the ability of a high resolution atmospheric chemistry model to reproduce observed relationships between meteorology and high or extreme O3. We employ regional coupled chemistry-transport model simulations to make three types of comparisons between simulated and observational data, comparing (1) tails of the O3 response variable, (2) distributions of meteorological predictor variables, and (3) sensitivities of high and extreme O3 to meteorological predictors. This last comparison is made using two methods: quantile regression, for the 0.95 quantile of O3, and tail dependence optimization, which is used to investigate even higher O3 extremes. Across all three locations, we find substantial differences between simulations and observational data in both meteorology and meteorological sensitivities of high and extreme O3.

  10. Surface chemistry of a pine-oil cleaner and other terpene mixtures with ozone on vinyl flooring tiles.

    Science.gov (United States)

    Ham, Jason E; Wells, J Raymond

    2011-04-01

    Indoor environments are dynamic reactors where consumer products (such as cleaning agents, deodorants, and air fresheners) emit volatile organic compounds (VOCs) that can subsequently interact with indoor oxidants such as ozone (O(3)), hydroxyl radicals, and nitrate radicals. Typically, consumer products consist of mixtures of VOCs and semi-VOCs which can react in the gas-phase or on surfaces with these oxidants to generate a variety of oxygenated products. In this study, the reaction of a pine-oil cleaner (POC) with O(3) (100ppb) on a urethane-coated vinyl flooring tile was investigated at 5% and 50% relative humidity. These results were compared to previous α-terpineol+O(3) reactions on glass and vinyl surfaces. Additionally, other terpene and terpene alcohol mixtures were formulated to understand the emission profiles as seen in the POC data. Results showed that the α-terpineol+O(3) reaction products were the prominent species that were also observed in the POC/O(3) surface experiments. Furthermore, α-terpineol+O(3) reactions generate the largest fraction of oxygenated products even in equal mixtures of other terpene alcohols. This finding suggests that the judicial choice of terpene alcohols for inclusion in product formulations may be useful in reducing oxidation product emissions. Published by Elsevier Ltd.

  11. Improved meteorology and ozone air quality simulations using MODIS land surface parameters in the Yangtze River Delta urban cluster, China

    Science.gov (United States)

    Li, Mengmeng; Wang, Tijian; Xie, Min; Zhuang, Bingliang; Li, Shu; Han, Yong; Song, Yu; Cheng, Nianliang

    2017-03-01

    Land surface parameters play an important role in the land-atmosphere coupling and thus are critical to the weather and dispersion of pollutants in the atmosphere. This work aims at improving the meteorology and air quality simulations for a high-ozone (O3) event in the Yangtze River Delta urban cluster of China, through incorporation of satellite-derived land surface parameters. Using Moderate Resolution Imaging Spectroradiometer (MODIS) input to specify the land cover type, green vegetation fraction, leaf area index, albedo, emissivity, and deep soil temperature provides a more realistic representation of surface characteristics. Preliminary evaluations reveal clearly improved meteorological simulation with MODIS input compared with that using default parameters, particularly for temperature (from -2.5 to -1.7°C for mean bias) and humidity (from 9.7% to 4.3% for mean bias). The improved meteorology propagates through the air quality system, which results in better estimates for surface NO2 (from 11.5 to 8.0 ppb for mean bias) and nocturnal O3 low-end concentration values (from -18.8 to -13.6 ppb for mean bias). Modifications of the urban land surface parameters are the main reason for model improvement. The deeper urban boundary layer and intense updraft induced by the urban heat island are favorable for pollutant dilution, thus contributing to lower NO2 and elevated nocturnal O3. Furthermore, the intensified sea-land breeze circulation may exacerbate O3 pollution at coastal cities through pollutant recirculation. Improvement of mesoscale meteorology and air quality simulations with satellite-derived land surface parameters will be useful for air pollution monitoring and forecasting in urban areas.

  12. Improvement of the prediction of surface ozone concentration over conterminous U.S. by a computationally efficient second-order Rosenbrock solver in CAM4-Chem

    Science.gov (United States)

    Sun, Jian; Fu, Joshua S.; Drake, John; Lamarque, Jean-Francois; Tilmes, Simone; Vitt, Francis

    2017-03-01

    The global chemistry-climate model (CAM4-Chem) overestimates the surface ozone concentration over the conterminous U.S. (CONUS). Reasons for this positive bias include emission, meteorology, chemical mechanism, and solver. In this study, we explore the last possibility by examining the sensitivity to the numerical methods for solving the chemistry equations. A second-order Rosenbrock (ROS-2) solver is implemented in CAM4-Chem to examine its influence on the surface ozone concentration and the computational performance of the chemistry program. Results show that under the same time step size (1800 s), statistically significant reduction of positive bias is achieved by the ROS-2 solver. The improvement is as large as 5.2 ppb in Eastern U.S. during summer season. The ROS-2 solver is shown to reduce the positive bias in Europe and Asia as well, indicating the lower surface ozone concentration over the CONUS predicted by the ROS-2 solver is not a trade-off consequence with increasing the ozone concentration at other global regions. In addition, by refining the time step size to 180 s, the first-order implicit solver does not provide statistically significant improvement of surface ozone concentration. It reveals that the better prediction from the ROS-2 solver is not only due to its accuracy but also due to its suitability for stiff chemistry equations. As an added benefit, the computation cost of the ROS-2 solver is almost half of first-order implicit solver. The improved computational efficiency of the ROS-2 solver is due to the reuse of the Jacobian matrix and lower upper (LU) factorization during its multistage calculation.

  13. Evaluation of broadband surface solar irradiance derived from the Ozone Monitoring Instrument

    NARCIS (Netherlands)

    Wang, P.; Sneep, M.; Veefkind, J.P.; Stammes, P.; Levelt, P.F.

    2014-01-01

    Surface solar irradiance (SSI) data are important for planning and estimating the production of solar power plants. Long-term high quality surface solar radiation data are needed for monitoring climate change. This paper presents a new surface solar irradiance dataset, the broadband (0.2–4 ?m)

  14. Adaptive-network-based fuzzy inference system (ANFIS modelbased prediction of the surface ozone concentration

    Directory of Open Access Journals (Sweden)

    Savić Marija

    2014-01-01

    Full Text Available This paper presents the results of the tropospheric ozone concentration modeling as the dependence on volatile organic compounds - VOCs (Benzene, Toluene, m,p-Xylene, o-Xylene, Ethylbenzene; nonorganic compounds - NOx (NO, NO2, NOx, CO, H2S, SO2 and PM10 in the ambient air in parallel with the meteorological parameters: temperature, solar radiation, relative humidity, wind speed and direction. Modeling is based on measured results obtained during the year 2009. The measurements were performed at the measuring station located within an agricultural area, in vicinity of city of Zrenjanin (Serbian Banat, Serbia. Statistical analysis of obtained data, based on bivariate correlation analysis indicated that accurate modeling cannot be performed using linear statistics approach. Also, considering that almost all input variables have wide range of relative change (ratio of variance compared to range, nonlinear statistic analysis method based on only one rule describing the behavior of input variable, most certainly wouldn’t present accurate enough results. From that reason, modeling approach was based on Adaptive-Network-Based Fuzzy Inference System (ANFIS. Model obtained using ANFIS methodology resulted with high accuracy, with prediction potential of above 80%, considering that obtained determination coefficient for the final model was R2=0.802.

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

    Science.gov (United States)

    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.…

  16. Bay breeze climatology at two sites along the Chesapeake bay from 1986-2010: Implications for surface ozone.

    Science.gov (United States)

    Stauffer, Ryan M; Thompson, Anne M

    Hourly surface meteorological measurements were coupled with surface ozone (O 3 ) mixing ratio measurements at Hampton, Virginia and Baltimore, Maryland, two sites along the Chesapeake Bay in the Mid-Atlantic United States, to examine the behavior of surface O 3 during bay breeze events and quantify the impact of the bay breeze on local O 3 pollution. Analyses were performed for the months of May through September for the years 1986 to 2010. The years were split into three groups to account for increasingly stringent environmental regulations that reduced regional emissions of nitrogen oxides (NO x ): 1986-1994, 1995-2002, and 2003-2010. Each day in the 25-year record was marked either as a bay breeze day, a non-bay breeze day, or a rainy/cloudy day based on the meteorological data. Mean eight hour (8-h) averaged surface O 3 values during bay breeze events were 3 to 5 parts per billion by volume (ppbv) higher at Hampton and Baltimore than on non-bay breeze days in all year periods. Anomalies from mean surface O 3 were highest in the afternoon at both sites during bay breeze days in the 2003-2010 study period. In conjunction with an overall lowering of baseline O 3 after the 1995-2002 period, the percentage of total exceedances of the Environmental Protection Agency (EPA) 75 ppbv 8-h O 3 standard that occurred on bay breeze days increased at Hampton for 2003-2010, while remaining steady at Baltimore. These results suggest that bay breeze circulations are becoming more important to causing exceedance events at particular sites in the region, and support the hypothesis of Martins et al. (2012) that highly localized meteorology increasingly drives air quality events at Hampton.

  17. Nobel prize awarded to pioneers in ozone research

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-12-31

    This article details the achievements of the three individuals who shared the 1995 Nobel Prize in Chemistry - Paul Crutzen, Mario Molina, and F. Sherwood Rowland - for their work in atmospheric chemistry, particularly the chemical processes that deplete the ozone layer. Background information about the ozone layer is presented as well as highlights of the ozone research done by the prize winners.

  18. The increasing threat to stratospheric ozone from dichloromethane.

    Science.gov (United States)

    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.

  19. Impacts of brown carbon from biomass burning on surface UV and ozone photochemistry in the Amazon Basin

    KAUST Repository

    Mok, Jungbin

    2016-11-11

    The spectral dependence of light absorption by atmospheric particulate matter has major implications for air quality and climate forcing, but remains uncertain especially in tropical areas with extensive biomass burning. In the September-October 2007 biomass-burning season in Santa Cruz, Bolivia, we studied light absorbing (chromophoric) organic or “brown” carbon (BrC) with surface and space-based remote sensing. We found that BrC has negligible absorption at visible wavelengths, but significant absorption and strong spectral dependence at UV wavelengths. Using the ground-based inversion of column effective imaginary refractive index in the range 305–368 nm, we quantified a strong spectral dependence of absorption by BrC in the UV and diminished ultraviolet B (UV-B) radiation reaching the surface. Reduced UV-B means less erythema, plant damage, and slower photolysis rates. We use a photochemical box model to show that relative to black carbon (BC) alone, the combined optical properties of BrC and BC slow the net rate of production of ozone by up to 18% and lead to reduced concentrations of radicals OH, HO2, and RO2 by up to 17%, 15%, and 14%, respectively. The optical properties of BrC aerosol change in subtle ways the generally adverse effects of smoke from biomass burning.

  20. Impacts of Brown Carbon from Biomass Burning on Surface UV and Ozone Photochemistry in the Amazon Basin

    Science.gov (United States)

    Mok, Jungbin; Krotkov, Nickolay A.; Arola, Antti; Torres, Omar; Jethva, Hiren; Andrade, Marcos; Labow, Gordon; Eck, Thomas F.; Li, Zhangqing; Dickerson, Russell R.; hide

    2016-01-01

    The spectral dependence of light absorption by atmospheric particulate matter has major implications for air quality and climate forcing, but remains uncertain especially in tropical areas with extensive biomass burning. In the September-October 2007 biomass-burning season in Santa Cruz, Bolivia, we studied light absorbing (chromophoric) organic or brown carbon (BrC) with surface and space-based remote sensing. We found that BrC has negligible absorption at visible wavelengths, but significant absorption and strong spectral dependence at UV wavelengths. Using the ground-based inversion of column effective imaginary refractive index in the range 305368nm, we quantified a strong spectral dependence of absorption by BrC in the UV and diminished ultraviolet B (UV-B) radiation reaching the surface. Reduced UV-B means less erythema, plant damage, and slower photolysis rates. We use a photochemical box model to show that relative to black carbon (BC) alone, the combined optical properties of BrC and BC slow the net rate of production of ozone by up to 18 and lead to reduced concentrations of radicals OH, HO2, and RO2 by up to 17, 15, and 14, respectively. The optical properties of BrC aerosol change in subtle ways the generally adverse effects of smoke from biomass burning.

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

    Science.gov (United States)

    Zadorozhny, Alexander; Dyominov, Igor

    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.

  2. Spectral analysis of atmospheric composition: application to surface ozone model–measurement comparisons

    Directory of Open Access Journals (Sweden)

    D. R. Bowdalo

    2016-07-01

    Full Text Available Models of atmospheric composition play an essential role in our scientific understanding of atmospheric processes and in providing policy strategies to deal with societally relevant problems such as climate change, air quality, and ecosystem degradation. The fidelity of these models needs to be assessed against observations to ensure that errors in model formulations are found and that model limitations are understood. A range of approaches are necessary for these comparisons. Here, we apply a spectral analysis methodology for this comparison. We use the Lomb–Scargle periodogram, a method similar to a Fourier transform, but better suited to deal with the gapped data sets typical of observational data. We apply this methodology to long-term hourly ozone observations and the equivalent model (GEOS-Chem output. We show that the spectrally transformed observational data show a distinct power spectrum with regimes indicative of meteorological processes (weather, macroweather and specific peaks observed at the daily and annual timescales together with corresponding harmonic peaks at one-half, one-third, etc., of these frequencies. Model output shows corresponding features. A comparison between the amplitude and phase of these peaks introduces a new comparison methodology between model and measurements. We focus on the amplitude and phase of diurnal and seasonal cycles and present observational/model comparisons and discuss model performance. We find large biases notably for the seasonal cycle in the mid-latitude Northern Hemisphere where the amplitudes are generally overestimated by up to 16 ppbv, and phases are too late on the order of 1–5 months. This spectral methodology can be applied to a range of model–measurement applications and is highly suitable for Multimodel Intercomparison Projects (MIPs.

  3. Photocatalytic ozonation of urban wastewater and surface water using immobilized TiO2 with LEDs: Micropollutants, antibiotic resistance genes and estrogenic activity.

    Science.gov (United States)

    Moreira, Nuno F F; Sousa, José M; Macedo, Gonçalo; Ribeiro, Ana R; Barreiros, Luisa; Pedrosa, Marta; Faria, Joaquim L; Pereira, M Fernando R; Castro-Silva, Sérgio; Segundo, Marcela A; Manaia, Célia M; Nunes, Olga C; Silva, Adrián M T

    2016-05-01

    Photocatalytic ozonation was employed for the first time in continuous mode with TiO2-coated glass Raschig rings and light emitting diodes (LEDs) to treat urban wastewater as well as surface water collected from the supply area of a drinking water treatment plant (DWTP). Different levels of contamination and types of contaminants were considered in this work, including chemical priority substances (PSs) and contaminants of emerging concern (CECs), as well as potential human opportunistic antibiotic resistant bacteria and their genes (ARB&ARG). Photocatalytic ozonation was more effective than single ozonation (or even than TiO2 catalytic ozonation) in the degradation of typical reaction by-products (such as oxalic acid), and more effective than photocatalysis to remove the parent micropollutants determined in urban wastewater. In fact, only fluoxetine, clarithromycin, erythromycin and 17-alpha-ethinylestradiol (EE2) were detected after photocatalytic ozonation, by using solid-phase extraction (SPE) pre-concentration and LC-MS/MS analysis. In surface water, this treatment allowed the removal of all determined micropollutants to levels below the limit of detection (0.01-0.20 ng L(-1)). The efficiency of this process was then assessed based on the capacity to remove different groups of cultivable microorganisms and housekeeping (16S rRNA) and antibiotic resistance or related genes (intI1, blaTEM, qnrS, sul1). Photocatalytic ozonation was observed to efficiently remove microorganisms and ARGs. Although after storage total heterotrophic and ARB (to ciprofloxacin, gentamicin, meropenem), fungi, and the genes 16S rRNA and intI1, increased to values close to the pre-treatment levels, the ARGs (blaTEM, qnrS and sul1) were reduced to levels below/close to the quantification limit even after 3-days storage of treated surface water or wastewater. Yeast estrogen screen (YES), thiazolyl blue tetrazolium reduction (MTT) and lactate dehydrogenase (LDH) assays were also performed

  4. Formation of a nano-pattering NiTi surface with Ni-depleted superficial layer to promote corrosion resistance and endothelial cell-material interaction.

    Science.gov (United States)

    Zhao, Tingting; Li, Yan; Xia, Yun; Venkatraman, Subbu S; Xiang, Yan; Zhao, Xinqing

    2013-01-01

    Zirconium ion implantation was performed on NiTi alloy to suppress Ni ion release as well as to improve corrosion resistance and cell-material interaction. A thicker Ni-depleted nano-scale composite layer formed after Zr implantation and the corrosion resistance was evidently increased in aspects of increased E(br) - E(corr) (difference between corrosion potential and breakdown potential) and decreased corrosion current density. 2.5/2 NiTi sample possessed the highest E(br) - E(corr), more than 500 mV higher than that of untreated NiTi, suggesting a significant improvement on pitting corrosion resistance. Ni ion release rate of Zr-NiTi was decreased due to the depletion of Ni in the superficial surface layer and the diffusion resistance effect of the ZrO(2)/TiO(2) nano-film. Increased surface wettability induced by increased surface roughness was obtained after Zr implantation. Zr-NiTi samples were found to be favorable to endothelial cells (ECs) proliferation, especially after 5 and 7 days culture.

  5. Design of a vehicle based system to prevent ozone loss

    Science.gov (United States)

    Lynn, Sean R.; Bunker, Deborah; Hesbach, Thomas D., Jr.; Howerton, Everett B.; Hreinsson, G.; Mistr, E. Kirk; Palmer, Matthew E.; Rogers, Claiborne; Tischler, Dayna S.; Wrona, Daniel J.

    1993-01-01

    Reduced quantities of ozone in the atmosphere allow greater levels of ultraviolet light (UV) radiation to reach the earth's surface. This is known to cause skin cancer and mutations. Chlorine liberated from Chlorofluorocarbons (CFC's) and natural sources initiate the destruction of stratospheric ozone through a free radical chain reaction. The project goals are to understand the processes which contribute to stratospheric ozone loss, examine ways to prevent ozone loss, and design a vehicle-based system to carry out the prevention scheme. The 1992/1993 design objectives were to accomplish the first two goals and define the requirements for an implementation vehicle to be designed in detail starting next year. Many different ozone intervention schemes have been proposed though few have been researched and none have been tested. A scheme proposed by R.J. Cicerone, Scott Elliot and R.P.Turco late in 1991 was selected because of its research support and economic feasibility. This scheme uses hydrocarbon injected into the Antarctic ozone hole to form stable compounds with free chlorine, thus reducing ozone depletion. Because most polar ozone depletion takes place during a 3-4 week period each year, the hydrocarbon must be injected during this time window. A study of the hydrocarbon injection requirements determined that 100 aircraft traveling Mach 2.4 at a maximum altitude of 66,000 ft. would provide the most economic approach to preventing ozone loss. Each aircraft would require an 8,000 nm. range and be able to carry 35,000 lbs. of propane. The propane would be stored in a three-tank high pressure system. Missions would be based from airport regions located in South America and Australia. To best provide the requirements of mission analysis, an aircraft with L/D(sub cruise) = 10.5, SFC = 0.65 (the faculty advisor suggested that this number is too low) and a 250,000 lb TOGW was selected as a baseline. Modularity and multi-role functionality were selected to be key

  6. The contribution of anthropogenic bromine emissions to past stratospheric ozone trends: a modelling study

    Directory of Open Access Journals (Sweden)

    B.-M. Sinnhuber

    2009-04-01

    Full Text Available Bromine compounds play an important role in the depletion of stratospheric ozone. We have calculated the changes in stratospheric ozone in response to changes in the halogen loading over the past decades, using a two-dimensional (latitude/height model constrained by source gas mixing ratios at the surface. Model calculations of the decrease of total column ozone since 1980 agree reasonably well with observed ozone trends, in particular when the contribution from very short-lived bromine compounds is included. Model calculations with bromine source gas mixing ratios fixed at 1959 levels, corresponding approximately to a situation with no anthropogenic bromine emissions, show an ozone column reduction between 1980 and 2005 at Northern Hemisphere mid-latitudes of only ≈55% compared to a model run including all halogen source gases. In this sense anthropogenic bromine emissions are responsible for ≈45% of the model estimated column ozone loss at Northern Hemisphere mid-latitudes. However, since a large fraction of the bromine induced ozone loss is due to the combined BrO/ClO catalytic cycle, the effect of bromine would have been smaller in the absence of anthropogenic chlorine emissions. The chemical efficiency of bromine relative to chlorine for global total ozone depletion from our model calculations, expressed by the so called α-factor, is 64 on an annual average. This value is much higher than previously published results. Updates in reaction rate constants can explain only part of the differences in α. The inclusion of bromine from very short-lived source gases has only a minor effect on the global mean α-factor.

  7. Coupling aerosol surface and bulk chemistry with a kinetic double layer model (K2-SUB: oxidation of oleic acid by ozone

    Directory of Open Access Journals (Sweden)

    C. Pfrang

    2010-05-01

    Full Text Available We present a kinetic double layer model coupling aerosol surface and bulk chemistry (K2-SUB based on the PRA framework of gas-particle interactions (Pöschl-Rudich-Ammann, 2007. K2-SUB is applied to a popular model system of atmospheric heterogeneous chemistry: the interaction of ozone with oleic acid. We show that our modelling approach allows de-convoluting surface and bulk processes, which has been a controversial topic and remains an important challenge for the understanding and description of atmospheric aerosol transformation. In particular, we demonstrate how a detailed treatment of adsorption and reaction at the surface can be coupled to a description of bulk reaction and transport that is consistent with traditional resistor model formulations.

    From literature data we have derived a consistent set of kinetic parameters that characterise mass transport and chemical reaction of ozone at the surface and in the bulk of oleic acid droplets. Due to the wide range of rate coefficients reported from different experimental studies, the exact proportions between surface and bulk reaction rates remain uncertain. Nevertheless, the model results suggest an important role of chemical reaction in the bulk and an approximate upper limit of ~10−11 cm2 s−1 for the surface reaction rate coefficient. Sensitivity studies show that the surface accommodation coefficient of the gas-phase reactant has a strong non-linear influence on both surface and bulk chemical reactions. We suggest that K2-SUB may be used to design, interpret and analyse future experiments for better discrimination between surface and bulk processes in the oleic acid-ozone system as well as in other heterogeneous reaction systems of atmospheric relevance.

  8. Changes in biologically-active ultraviolet radiation reaching the Earth's surface.

    Science.gov (United States)

    McKenzie, R L; Aucamp, P J; Bais, A F; Björn, L O; Ilyas, M

    2007-03-01

    The Montreal Protocol is working. Concentrations of major ozone-depleting substances in the atmosphere are now decreasing, and the decline in total column amounts seen in the 1980s and 1990s at mid-latitudes has not continued. In polar regions, there is much greater natural variability. Each spring, large ozone holes continue to occur in Antarctica and less severe regions of depleted ozone continue to occur in the Arctic. There is evidence that some of these changes are driven by changes in atmospheric circulation rather than being solely attributable to reductions in ozone-depleting substances, which may indicate a linkage to climate change. Global ozone is still lower than in the 1970s and a return to that state is not expected for several decades. As changes in ozone impinge directly on UV radiation, elevated UV radiation due to reduced ozone is expected to continue over that period. Long-term changes in UV-B due to ozone depletion are difficult to verify through direct measurement, but there is strong evidence that UV-B irradiance increased over the period of ozone depletion. At unpolluted sites in the southern hemisphere, there is some evidence that UV-B irradiance has diminished since the late 1990s. The availability and temporal extent of UV data have improved, and we are now able to evaluate the changes in recent times compared with those estimated since the late 1920s, when ozone measurements first became available. The increases in UV-B irradiance over the latter part of the 20th century have been larger than the natural variability. There is increased evidence that aerosols have a larger effect on surface UV-B radiation than previously thought. At some sites in the Northern Hemisphere, UV-B irradiance may continue to increase because of continuing reductions in aerosol extinctions since the 1990s. Interactions between ozone depletion and climate change are complex and can be mediated through changes in chemistry, radiation, and atmospheric circulation

  9. The search for signs of recovery of the ozone layer.

    Science.gov (United States)

    Weatherhead, Elizabeth C; Andersen, Signe Bech

    2006-05-04

    Evidence of mid-latitude ozone depletion and proof that the Antarctic ozone hole was caused by humans spurred policy makers from the late 1980s onwards to ratify the Montreal Protocol and subsequent treaties, legislating for reduced production of ozone-depleting substances. The case of anthropogenic ozone loss has often been cited since as a success story of international agreements in the regulation of environmental pollution. Although recent data suggest that total column ozone abundances have at least not decreased over the past eight years for most of the world, it is still uncertain whether this improvement is actually attributable to the observed decline in the amount of ozone-depleting substances in the Earth's atmosphere. The high natural variability in ozone abundances, due in part to the solar cycle as well as changes in transport and temperature, could override the relatively small changes expected from the recent decrease in ozone-depleting substances. Whatever the benefits of the Montreal agreement, recovery of ozone is likely to occur in a different atmospheric environment, with changes expected in atmospheric transport, temperature and important trace gases. It is therefore unlikely that ozone will stabilize at levels observed before 1980, when a decline in ozone concentrations was first observed.

  10. Comment on ``Theory of the photodissociation of ozone in the Hartley continuum: Potential energy surfaces, conical intersections, and photodissociation dynamics'' [J. Chem. Phys. 123, 014306 (2005)

    Science.gov (United States)

    Grebenshchikov, S. Yu.; Schinke, R.

    2007-06-01

    We demonstrate in this Comment that the quantum mechanical absorption spectrum of the Hartley band of ozone, calculated using the diabatic B state potential energy surface constructed from the ab initio data of the title paper, is strongly structured. This result, which is in agreement with previous theoretical studies of the Hartley band, contradicts the findings of Baloïtcha and Balint-Kurti and questions the accuracy of their calculations.

  11. UV and infrared absorption spectra, atmospheric lifetimes, and ozone depletion and global warming potentials for CCl2FCCl2F (CFC-112, CCl3CClF2 (CFC-112a, CCl3CF3 (CFC-113a, and CCl2FCF3 (CFC-114a

    Directory of Open Access Journals (Sweden)

    M. E. Davis

    2016-07-01

    Full Text Available The potential impact of CCl2FCF3 (CFC-114a and the recently observed CCl2FCCl2F (CFC-112, CCl3CClF2 (CFC-112a, and CCl3CF3 (CFC-113a chlorofluorocarbons (CFCs on stratospheric ozone and climate is presently not well characterized. In this study, the UV absorption spectra of these CFCs were measured between 192.5 and 235 nm over the temperature range 207–323 K. Precise parameterizations of the UV absorption spectra are presented. A 2-D atmospheric model was used to evaluate the CFC atmospheric loss processes, lifetimes, ozone depletion potentials (ODPs, and the associated uncertainty ranges in these metrics due to the kinetic and photochemical uncertainty. The CFCs are primarily removed in the stratosphere by short-wavelength UV photolysis with calculated global annually averaged steady-state lifetimes (years of 63.6 (61.9–64.7, 51.5 (50.0–52.6, 55.4 (54.3–56.3, and 105.3 (102.9–107.4 for CFC-112, CFC-112a, CFC-113a, and CFC-114a, respectively. The range of lifetimes given in parentheses is due to the 2σ uncertainty in the UV absorption spectra and O(1D rate coefficients included in the model calculations. The 2-D model was also used to calculate the CFC ozone depletion potentials (ODPs with values of 0.98, 0.86, 0.73, and 0.72 obtained for CFC-112, CFC-112a, CFC-113a, and CFC-114a, respectively. Using the infrared absorption spectra and lifetimes determined in this work, the CFC global warming potentials (GWPs were estimated to be 4260 (CFC-112, 3330 (CFC-112a, 3650 (CFC-113a, and 6510 (CFC-114a for the 100-year time horizon.

  12. Reply to "Comment on 'Cosmic-ray-driven reaction and greenhouse effect of halogenated molecules: Culprits for atmospheric ozone depletion and global climate change' by Rolf Müller and Jens-Uwe Grooß"

    Science.gov (United States)

    Lu, Q.-B.

    2014-04-01

    In their Comment, Müller and Grooß continuously use problematic "observed data" and misleading arguments to make a case against our CRE mechanism of the ozone hole and CFC-warming mechanism of global climate change. They make the groundless assertion that the CRE theory cannot be considered as an independent process for ozone loss in the polar stratosphere. Their claim that the impact of the CRE mechanism on polar chlorine activation and ozone loss in the stratosphere would be limited does not agree with the observed data over the past decades. They also make many contradictory and fact-distorting arguments that "There is no polar ozone loss in darkness, there is no apparent 11-year periodicity in polar total ozone measurements, the age of air in the polar lower stratosphere is much older than 1-2 years, and the reported detection of a pronounced recovery (by about 20-25%) in Antarctic total ozone measurements by the year 2010 is in error." These assertions ignore and contradict a great deal of robust observed data from both laboratory and field measurements reported in the literature including their own publications. Their new argument for the photodissociation of CFCs on PSCs also contradicts their previous extraordinary efforts including the use of fabricated "ACE-FTS satellite data" to argue for no physical/chemical loss of CFCs in the winter lower polar stratosphere. Finally, they do not provide any scientific evidence to support their criticism for the no physical basis of the CFC-warming theory and its conclusions. In summary, their misleading arguments and false "data" do not change the convincing conclusion reached by robust observations in my recent paper that both the CRE mechanism and the CFC-warming mechanism not only provide new fundamental understandings of the O3 hole and global climate change but have superior predictive capabilities, compared with the conventional models.

  13. Formaldehyde Column Density Measurements as a Suitable Pathway to Estimate Near-Surface Ozone Tendencies from Space

    Science.gov (United States)

    Schroeder, Jason R.; Crawford, James H.; Fried, Alan; Walega, James; Weinheimer, Andrew; Wisthaler, Armin; Mueller, Markus; Mikoviny, Tomas; Chen, Gao; Shook, Michael; hide

    2016-01-01

    In support of future satellite missions that aim to address the current shortcomings in measuring air quality from space, NASA's Deriving Information on Surface Conditions from Column and Vertically Resolved Observations Relevant to Air Quality (DISCOVER-AQ) field campaign was designed to enable exploration of relationships between column measurements of trace species relevant to air quality at high spatial and temporal resolution. In the DISCOVER-AQ data set, a modest correlation (r2 = 0.45) between ozone (O3) and formaldehyde (CH2O) column densities was observed. Further analysis revealed regional variability in the O3-CH2O relationship, with Maryland having a strong relationship when data were viewed temporally and Houston having a strong relationship when data were viewed spatially. These differences in regional behavior are attributed to differences in volatile organic compound (VOC) emissions. In Maryland, biogenic VOCs were responsible for approx.28% of CH2O formation within the boundary layer column, causing CH2O to, in general, increase monotonically throughout the day. In Houston, persistent anthropogenic emissions dominated the local hydrocarbon environment, and no discernable diurnal trend in CH2O was observed. Box model simulations suggested that ambient CH2O mixing ratios have a weak diurnal trend (+/-20% throughout the day) due to photochemical effects, and that larger diurnal trends are associated with changes in hydrocarbon precursors. Finally, mathematical relationships were developed from first principles and were able to replicate the different behaviors seen in Maryland and Houston. While studies would be necessary to validate these results and determine the regional applicability of the O3-CH2O relationship, the results presented here provide compelling insight into the ability of future satellite missions to aid in monitoring near-surface air quality.

  14. Surface reaction mechanisms during ozone and oxygen plasma assisted atomic layer deposition of aluminum oxide.

    Science.gov (United States)

    Rai, Vikrant R; Vandalon, Vincent; Agarwal, Sumit

    2010-09-07

    We have elucidated the reaction mechanism and the role of the reactive intermediates in the atomic layer deposition (ALD) of aluminum oxide from trimethyl aluminum in conjunction with O(3) and an O(2) plasma. In situ attenuated total reflection Fourier transform infrared spectroscopy data show that both -OH groups and carbonates are formed on the surface during the oxidation cycle. These carbonates, once formed on the surface, are stable to prolonged O(3) exposure in the same cycle. However, in the case of plasma-assisted ALD, the carbonates decompose upon prolonged O(2) plasma exposure via a series reaction kinetics of the type, A (CH(3)) --> B (carbonates) --> C (Al(2)O(3)). The ratio of -OH groups to carbonates on the surface strongly depends on the oxidizing agent, and also the duration of the oxidation cycle in plasma-assisted ALD. However, in both O(3) and O(2) plasma cycles, carbonates are a small fraction of the total number of reactive sites compared to the hydroxyl groups.

  15. Bromide Sources and Loads in Swiss Surface Waters and Their Relevance for Bromate Formation during Wastewater Ozonation.

    Science.gov (United States)

    Soltermann, Fabian; Abegglen, Christian; Götz, Christian; von Gunten, Urs

    2016-09-20

    Bromide measurements and mass balances in the catchments of major Swiss rivers revealed that chemical industry and municipal waste incinerators are the most important bromide sources and account for ∼50% and ∼20%, respectively, of the ∼2000 tons of bromide discharged in the Rhine river in 2014 in Switzerland. About 100 wastewater treatment plants (WWTPs) will upgrade their treatment for micropollutant abatement in the future to comply with Swiss regulations. An upgrade with ozonation may lead to unintended bromate formation in bromide-containing wastewaters. Measured bromide concentrations were industry). Wastewater ozonation formed little bromate at specific ozone doses of ≤0.4 mg O3/mg DOC, while the bromate yields were almost linearly correlated to the specific ozone dose for higher ozone doses. Molar bromate yields for typical specific ozone doses in wastewater treatment (0.4-0.6 mg O3/mg DOC) are ≤3%. In a modeled extreme scenario (in which all upgraded WWTPs release 10 μg L(-1) of bromate), bromate concentrations increased by major Swiss rivers and by several micrograms per liter in receiving water bodies with a high fraction of municipal wastewater.

  16. Intrinsic Depletion or Not

    DEFF Research Database (Denmark)

    Klösgen, Beate; Bruun, Sara; Hansen, Søren

      The presence of a depletion layer of water along extended hydrophobic interfaces, and a possibly related formation of nanobubbles, is an ongoing discussion. The phenomenon was initially reported when we, years ago, chose thick films (~300-400Å) of polystyrene as cushions between a crystalline...... carrier and biomimetic membranes deposited thereupon and exposed to bulk water. While monitoring the sequential build-up of the sandwiched composite structure by continuous neutron reflectivity experiments the formation of an unexpected additional layer was detected (1). Located at the polystyrene surface...... in between he polymer cushion and bulk water the layer was attributed to water of reduced density and was called "depletion layer".  Impurities or preparative artefacts were excluded as its origin. Later on, the formation of nanobubbles from this vapour-like water phase was initiated by tipping the surface...

  17. Ozone Depletion, Greenhouse Gases, and Climate Change. Proceedings of a Joint Symposium by the Board on Atmospheric Sciences and Climate and the Committee on Global Change, National Research Council (Washington, D.C., March 23, 1988).

    Science.gov (United States)

    National Academy of Sciences - National Research Council, Washington, DC.

    The motivation for the organization of this symposium was the accumulation of evidence from many sources, both short- and long-term, that the global climate is in a state of change. Data which defy integrated explanation including temperature, ozone, methane, precipitation and other climate-related trends have presented troubling problems for…

  18. Phase space barriers and dividing surfaces in the absence of critical points of the potential energy: Application to roaming in ozone

    Energy Technology Data Exchange (ETDEWEB)

    Mauguière, Frédéric A. L., E-mail: frederic.mauguiere@bristol.ac.uk; Collins, Peter, E-mail: peter.collins@bristol.ac.uk; Wiggins, Stephen, E-mail: stephen.wiggins@mac.com [School of Mathematics, University of Bristol, Bristol BS8 1TW (United Kingdom); Kramer, Zeb C., E-mail: zebcolterkramer@gmail.com; Ezra, Gregory S., E-mail: gse1@cornell.edu [Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York 14853 (United States); Carpenter, Barry K., E-mail: carpenterb1@cardiff.ac.uk [School of Chemistry, Cardiff University, Cardiff CF10 3AT (United Kingdom); Farantos, Stavros C., E-mail: farantos@iesl.forth.gr [Institute of Electronic Structure and Laser, Foundation for Research and Technology - Hellas, and Department of Chemistry, University of Crete, Iraklion 711 10, Crete (Greece)

    2016-02-07

    We examine the phase space structures that govern reaction dynamics in the absence of critical points on the potential energy surface. We show that in the vicinity of hyperbolic invariant tori, it is possible to define phase space dividing surfaces that are analogous to the dividing surfaces governing transition from reactants to products near a critical point of the potential energy surface. We investigate the problem of capture of an atom by a diatomic molecule and show that a normally hyperbolic invariant manifold exists at large atom-diatom distances, away from any critical points on the potential. This normally hyperbolic invariant manifold is the anchor for the construction of a dividing surface in phase space, which defines the outer or loose transition state governing capture dynamics. We present an algorithm for sampling an approximate capture dividing surface, and apply our methods to the recombination of the ozone molecule. We treat both 2 and 3 degrees of freedom models with zero total angular momentum. We have located the normally hyperbolic invariant manifold from which the orbiting (outer) transition state is constructed. This forms the basis for our analysis of trajectories for ozone in general, but with particular emphasis on the roaming trajectories.

  19. The ocean's role in polar climate change: asymmetric Arctic and Antarctic responses to greenhouse gas and ozone forcing.

    Science.gov (United States)

    Marshall, John; Armour, Kyle C; Scott, Jeffery R; Kostov, Yavor; Hausmann, Ute; Ferreira, David; Shepherd, Theodore G; Bitz, Cecilia M

    2014-07-13

    In recent decades, the Arctic has been warming and sea ice disappearing. By contrast, the Southern Ocean around Antarctica has been (mainly) cooling and sea-ice extent growing. We argue here that interhemispheric asymmetries in the mean ocean circulation, with sinking in the northern North Atlantic and upwelling around Antarctica, strongly influence the sea-surface temperature (SST) response to anthropogenic greenhouse gas (GHG) forcing, accelerating warming in the Arctic while delaying it in the Antarctic. Furthermore, while the amplitude of GHG forcing has been similar at the poles, significant ozone depletion only occurs over Antarctica. We suggest that the initial response of SST around Antarctica to ozone depletion is one of cooling and only later adds to the GHG-induced warming trend as upwelling of sub-surface warm water associated with stronger surface westerlies impacts surface properties. We organize our discussion around 'climate response functions' (CRFs), i.e. the response of the climate to 'step' changes in anthropogenic forcing in which GHG and/or ozone-hole forcing is abruptly turned on and the transient response of the climate revealed and studied. Convolutions of known or postulated GHG and ozone-hole forcing functions with their respective CRFs then yield the transient forced SST response (implied by linear response theory), providing a context for discussion of the differing warming/cooling trends in the Arctic and Antarctic. We speculate that the period through which we are now passing may be one in which the delayed warming of SST associated with GHG forcing around Antarctica is largely cancelled by the cooling effects associated with the ozone hole. By mid-century, however, ozone-hole effects may instead be adding to GHG warming around Antarctica but with diminished amplitude as the ozone hole heals. The Arctic, meanwhile, responding to GHG forcing but in a manner amplified by ocean heat transport, may continue to warm at an accelerating rate.

  20. Experimental and modelling study of the effect of airflow orientation with respect to strip electrode on ozone production of surface dielectric barrier discharge

    Science.gov (United States)

    Mikeš, J.; Pekárek, S.; Soukup, I.

    2016-11-01

    This study examines the effect of airflow orientation with respect to the strip active electrode on concentration of ozone and nitrogen dioxide produced in a planar generator based on the surface dielectric barrier discharge. The orientation of the airflow was tested in parallel and perpendicular with respect to the strips. It was found that in the investigated range of average discharge power, the ozone concentration increases approximately by 25% when airflow was oriented in parallel with respect to the strips in comparison with perpendicular orientation of the airflow. Similarly the increase of nitrogen dioxide concentration was observed for parallel orientation of the airflow with respect to the strips in comparison with the perpendicular orientation of the airflow. Within the range of wavelengths from 250 to 1100 nm, the changes of intensities of spectral lines associated with airflow orientation have been observed. A 3D numerical model describing ion trajectories and airflow patterns have also been developed.

  1. Leukocytes-depleting filters preferentially remove activated leukocytes and reduce the expression of surface adhesion molecules during the simulated extracorporeal circulation of human blood.

    Science.gov (United States)

    Alexiou, Christos; Sheppard, Stuart; Tang, Augustine; Rengarajan, Arvind; Smith, David; Haw, Marcus; Gibbs, Roz

    2006-01-01

    The effect of leukocyte-depleting filters on the total and activated leukocyte counts and the expression of surface adhesion molecules CD11b, CD18, and CD62L during the in vitro extracorporeal circulation of human blood was studied. A 200 ml blood sample was taken from 10 patients undergoing CABG surgery. The blood was circulated for 60 minutes within an experimental extracorporeal circuit. A leukocyte-depleting filter was attached in five circuits (filtered group). In five other circuits, no filter was used (controls). Total leukocyte counts were determined manually. Activated leukocytes were identified using nitroblue tetrazolium staining. The expression of CD11b, CD18, and CD62L was measured with flow cytometry. At 60 minutes, total leukocyte counts were reduced by 49% from the baseline values in the filtered group and 10% in the control group (p filtered group and increased by 116% in the control group (p filtered group, the expression of CD11b, CD18, and CD612L decreased by 60%, 21%, and 79%, respectively, and in the control group it increased by 24%, 6%, and 28% (p filters preferentially remove activated leukocytes and reduce the expression of CD11b, CD18, and CD62L during the in vitro extracorporeal circulation of human blood.

  2. Sensitivity of δ15N of nitrate, surface suspended and deep sinking particulate nitrogen to seasonal nitrate depletion in the Southern Ocean

    Science.gov (United States)

    Lourey, Martin J.; Trull, Thomas W.; Sigman, Daniel M.

    2003-09-01

    We report measurements of the δ15N of nitrate, suspended particulate nitrogen (PN), and sinking PN from cruises and moored sediment traps in the Subantarctic Zone (SAZ) and Polar Frontal Zone (PFZ) south of Australia. As expected, surface water nitrate δ15N increased as nitrate was consumed during the spring/summer bloom. In contrast, the seasonal cycles of surface water suspended and sinking PN δ15N did not fit expectations from nitrate assimilation alone. Rather than increasing, the δ15N of surface suspended PN was relatively constant in the SAZ (at ˜1‰), and decreased during the summer in the PFZ (from ˜0 to ˜-4‰), most likely due to the production of low 15N PN by summertime ammonium recycling. Deep sediment trap PN δ15N also displayed seasonal decreases (from ˜4 to ˜1‰ in the SAZ, and from ˜3.5 to ˜0.5‰ in the PFZ), which correlated with PON flux magnitude. During high-flux periods, exported PN δ15N values were close to expectations from nitrate-based export, but low-flux periods exhibited higher δ15N, consistent with either a reduction in the isotope effect of nitrate assimilation or more extensive isotopic alteration of the sinking material during low-flux periods. The mass balance between net nitrate supply and exported PN that links sinking flux δ15N to nitrate utilization requires only that the annually integrated (rather than the seasonally varying) sinking flux of PN δ15N correlates with nitrate depletion. While a correlation between annually integrated sinking PN δ15N to nitrate depletion was observed in both the SAZ and PFZ, the sensitivity of sinking PN δ15N to nitrate depletion was lower than expected. Moreover, the seasonal observations raise the possibility that loss of the summertime high-flux period represents an alternative explanation to increased nitrate utilization for the high sedimentary PN δ15N observed during glacial periods.

  3. Assessment of groundwater/surface-water interaction and simulation of potential streamflow depletion induced by groundwater withdrawal, Uinta River near Roosevelt, Utah

    Science.gov (United States)

    Lambert, P.M.; Marston, T.; Kimball, B.A.; Stolp, B.J.

    2011-01-01

    Roosevelt City, Utah, asserts a need for an additional supply of water to meet municipal demands and has identified a potential location for additional groundwater development at the Sprouse well field near the West Channel of the Uinta River. Groundwater is commonly hydraulically linked to surface water and, under some conditions, the pumpage of groundwater can deplete water in streams and other water bodies. In 2008, the U.S. Geological Survey, in cooperation with Roosevelt City, the Utah Department of Natural Resources, and the Ute Indian Tribe, began a study to improve understanding of the local interconnection between groundwater and surface water and to assess the potential for streamflow depletion from future groundwater withdrawals at a potential Roosevelt City development location—the Sprouse well field near the West Channel of the Uinta River.In the study, streamflow gains and losses at the river/aquifer boundary near the well field and changes in those conditions over time were assessed through (1) synoptic measurement of discharge in the stream at multiple sites using tracer-dilution methods, (2) periodic measurement of the vertical hydraulic gradient across the streambed, and (3) continuous measurement of stream and streambed water temperature using heat as a tracer of flow across the streambed. Although some contradictions among the results of the three assessment methods were observed, results of the approaches generally indicated (1) losing streamflow conditions on the West Channel of the Uinta River north of and upstream from the Sprouse well field within the study area, (2) gaining streamflow conditions south of and downstream from the well field, and (3) some seasonal changes in those conditions that correspond with seasonal changes in stream stage and local water-table altitudes.A numerical groundwater flow model was developed on the basis of previously reported observations and observations made during this study, and was used to estimate

  4. Ionic depletion at the crystalline Gibbs layer of PEG-capped gold nanoparticle brushes at aqueous surfaces

    Science.gov (United States)

    Wang, Wenjie; Zhang, Honghu; Mallapragada, Surya; Travesset, Alex; Vaknin, David

    2017-12-01

    In situ surface-sensitive x-ray diffraction and grazing incidence x-ray fluorescence spectroscopy (GIXFS) methods are combined to determine the ionic distributions across the liquid/vapor interfaces of thiolated-polyethylene-glycol-capped gold nanoparticle (PEG-AuNP) solutions. Induced by the addition of salts (i.e., Cs2SO4 ) to PEG-AuNPs solutions, two-dimensional hexagonal lattices of PEG-AuNPs form spontaneously at the aqueous surfaces, as is demonstrated by x-ray reflectivity and grazing incidence small-angle x-ray scattering. By taking advantage of element specificity with the GIXFS method, we find that the cation Cs+ concentration at the crystalline film is significantly reduced in parts of the PEG-AuNP film compared with that in the bulk.

  5. Ozone-induced climate change propped up by the Southern Hemisphere oceanic front

    Science.gov (United States)

    Ogawa, Fumiaki; Omrani, Nour-Eddine; Nishii, Kazuaki; Nakamura, Hisashi; Keenlyside, Noel

    2015-11-01

    The late twentieth century was marked by a significant summertime trend in the Southern Annular Mode (SAM), the dominant mode of tropospheric variability in the extratropical Southern Hemisphere (SH). This trend with poleward shifting tropospheric westerlies was attributed to downward propagation of stratospheric changes induced by ozone depletion. However, the role of the ocean in setting the SAM response to ozone depletion and its dynamical forcing remains unclear. Here we show, using idealized experiments with a state-of-the-art atmospheric model and analysis of Intergovernmental Panel on Climate Change climate simulations, that frontal sea surface temperature gradients in the midlatitude SH are critical for translating the ozone-induced stratospheric changes down to the surface. This happens through excitation of wave forcing, which controls the vertical connection of the tropospheric SAM with the stratosphere and shows the importance of internal tropospheric dynamics for stratosphere/troposphere coupling. Thus, improved simulation of oceanic fronts may reduce uncertainties in simulating SH ozone-induced climate changes.

  6. A diabatic circulation two-dimensional model with photochemistry - Simulations of ozone and long-lived tracers with surface sources

    Science.gov (United States)

    Stordal, F.; Isaksen, I. S. A.; Horntveth, K.

    1985-01-01

    Numerous studies have been concerned with the possibility of a reduction of the stratospheric ozone layer. Such a reduction could lead to an enhanced penetration of ultraviolet (UV) radiation to the ground, and, as a result, to damage in the case of several biological processes. It is pointed out that the distributions of many trace gases, such as ozone, are governed in part by transport processes. The present investigation presents a two-dimensional photochemistry-transport model using the residual circulation. The global distribution of both ozone and components with ground sources computed in this model is in good agreement with the observations even though slow diffusion is adopted. The agreement is particularly good in the Northern Hemisphere. The results provide additional support for the idea that tracer transport in the stratosphere is mainly of advective nature.

  7. Surface ozone over southern Africa; synthesis of monitoring results during the cross border air pollution impact assessment project

    CSIR Research Space (South Africa)

    Zunckel, M

    2004-11-01

    Full Text Available - efstroom University for CHE. Diab, R.D., Thompson, A.M., Zunckel, M., Coetzee, G.J.R., Combrink, J., Bodeker, G.E., Fishman, J., Sokolic, F., McNamara, D.P., Archer, C.B., Nganga, D., 1996. Vertical ozone distribution over southern Africaand adjacent oceans....A., Johnson, B.J., Shadwick, D.S., Cuevas, E., Schmidlin, F.J., Tarasick, D.W., Claude, H., Kerr, J.B., Uchino, O., 1998. Trends of ozone in the troposphere. Geophysical Research Letters 25 (2), 139?142. Scheel, H.E., Sladkovic, R., Brunke, E-G., Seiler, W...

  8. Transpacific transport of ozone pollution and the effect of recent Asian emission increases on air quality in North America: an integrated analysis using satellite, aircraft, ozonesonde, and surface observations

    Directory of Open Access Journals (Sweden)

    L. Zhang

    2008-10-01

    Full Text Available We use an ensemble of aircraft, satellite, sonde, and surface observations for April–May 2006 (NASA/INTEX-B aircraft campaign to better understand the mechanisms for transpacific ozone pollution and its implications for North American air quality. The observations are interpreted with a global 3-D chemical transport model (GEOS-Chem. OMI NO2 satellite observations constrain Asian anthropogenic NOx emissions and indicate a factor of 2 increase from 2000 to 2006 in China. Satellite observations of CO from AIRS and TES indicate two major events of Asian transpacific pollution during INTEX-B. Correlation between TES CO and ozone observations shows evidence for transpacific ozone pollution. The semi-permanent Pacific High and Aleutian Low cause splitting of transpacific pollution plumes over the Northeast Pacific. The northern branch circulates around the Aleutian Low and has little impact on North America. The southern branch circulates around the Pacific High and some of that air impacts western North America. Both aircraft measurements and model results show sustained ozone production driven by peroxyacetylnitrate (PAN decomposition in the southern branch, roughly doubling the transpacific influence from ozone produced in the Asian boundary layer. Model simulation of ozone observations at Mt. Bachelor Observatory in Oregon (2.7 km altitude indicates a mean Asian ozone pollution contribution of 9±3 ppbv to the mean observed concentration of 54 ppbv, reflecting mostly an enhancement in background ozone rather than episodic Asian plumes. Asian pollution enhanced surface ozone concentrations by 5–7 ppbv over western North America in spring 2006. The 2000–2006 rise in Asian anthropogenic emissions increased this influence by 1–2 ppbv.

  9. On-farm irrigation reservoirs for surface water storage in eastern Arkansas: Trends in construction in response to aquifer depletion

    Science.gov (United States)

    Yaeger, M. A.; Reba, M. L.; Massey, J. H.; Adviento-Borbe, A.

    2017-12-01

    On-farm surface water storage reservoirs have been constructed to address declines in the Mississippi River Valley Alluvial aquifer, the primary source of irrigation for most of the row crops grown in eastern Arkansas. These reservoirs and their associated infrastructure represent significant investments in financial and natural resources, and may cause producers to incur costs associated with foregone crop production and long-term maintenance. Thus, an analysis of reservoir construction trends in the Grand Prairie Critical Groundwater Area (GPCGA) and Cache River Critical Groundwater Area (CRCGA) was conducted to assist future water management decisions. Between 1996 and 2015, on average, 16 and 4 reservoirs were constructed per year, corresponding to cumulative new reservoir surface areas of 161 and 60 ha yr-1, for the GPCGA and the CRCGA, respectively. In terms of reservoir locations relative to aquifer status, after 1996, 84.5% of 309 total reservoirs constructed in the GPCGA and 91.0% of 78 in the CRCGA were located in areas with remaining saturated aquifer thicknesses of 50% or less. The majority of new reservoirs (74% in the GPCGA and 63% in the CRCGA) were constructed on previously productive cropland. The next most common land use, representing 11% and 15% of new reservoirs constructed in the GPCGA and CRCGA, respectively, was the combination of a field edge and a ditch, stream, or other low-lying area. Less than 10% of post-1996 reservoirs were constructed on predominately low-lying land, and the use of such lands decreased in both critical groundwater areas during the past 20 years. These disparities in reservoir construction rates, locations, and prior land uses is likely due to groundwater declines being first observed in the GPCGA as well as the existence of two large-scale river diversion projects under construction in the GPCGA that feature on-farm storage as a means to offset groundwater use.

  10. Generation of ozone by pulsed corona discharge over water surface in hybrid gas-liquid electrical discharge reactor

    Czech Academy of Sciences Publication Activity Database

    Lukeš, Petr; Člupek, Martin; Babický, Václav; Šunka, Pavel; Janda, V.

    2005-01-01

    Roč. 38, č. 3 (2005), s. 409-416 ISSN 0022-3727 R&D Projects: GA ČR(CZ) GA202/02/1026 Institutional research plan: CEZ:AV0Z20430508 Keywords : Corona disc harge * hybrid reactor * ozone * water treatment Subject RIV: BL - Plasma and Gas Disc harge Physics Impact factor: 1.957, year: 2005

  11. Surface and boundary layer exchanges of volatile organic compounds, nitrogen oxides and ozone during the GABRIEL campaign

    NARCIS (Netherlands)

    Ganzeveld, L.; Eerdekens, G.; Feig, G.; Fischer, H.; Harder, H.; Konigstedt, R.; Kubistin, D.; Martinez, M.; Meixner, F. X.; Scheeren, H. A.; Sinha, V.; Taraborrelli, D.; Williams, J.; de Arellano, J. Vila-Guerau; Lelieveld, J.

    2008-01-01

    We present an evaluation of sources, sinks and turbulent transport of nitrogen oxides, ozone and volatile organic compounds (VOC) in the boundary layer over French Guyana and Suriname during the October 2005 GABRIEL campaign by simulating observations with a single-column chemistry and climate model

  12. Reductions in bacterial microorganisms by filtration and ozonation of the surface water supply at the USFWS Northeast Fishery Center

    Science.gov (United States)

    A water filtration and ozonation system was recently installed to treat creek water used to culture species of concern at the U.S. Fish and Wildlife Service's Northeast Fishery Center, Lamar National Fish Hatchery (NFH). Past experience with fish culture indicates that the following bacterial pathog...

  13. Intra-urban spatial variability of surface ozone in Riverside, CA: viability and validation of low-cost sensors

    Science.gov (United States)

    Sadighi, Kira; Coffey, Evan; Polidori, Andrea; Feenstra, Brandon; Lv, Qin; Henze, Daven K.; Hannigan, Michael

    2018-03-01

    Sensor networks are being more widely used to characterize and understand compounds in the atmosphere like ozone (O3). This study employs a measurement tool, called the U-Pod, constructed at the University of Colorado Boulder, to investigate spatial and temporal variability of O3 in a 200 km2 area of Riverside County near Los Angeles, California. This tool contains low-cost sensors to collect ambient data at non-permanent locations. The U-Pods were calibrated using a pre-deployment field calibration technique; all the U-Pods were collocated with regulatory monitors. After collocation, the U-Pods were deployed in the area mentioned. A subset of pods was deployed at two local regulatory air quality monitoring stations providing validation for the collocation calibration method. Field validation of sensor O3 measurements to minute-resolution reference observations resulted in R2 and root mean squared errors (RMSEs) of 0.95-0.97 and 4.4-5.9 ppbv, respectively. Using the deployment data, ozone concentrations were observed to vary on this small spatial scale. In the analysis based on hourly binned data, the median R2 values between all possible U-Pod pairs varied from 0.52 to 0.86 for ozone during the deployment. The medians of absolute differences were calculated between all possible pod pairs, 21 pairs total. The median values of those median absolute differences for each hour of the day varied between 2.2 and 9.3 ppbv for the ozone deployment. Since median differences between U-Pod concentrations during deployment are larger than the respective root mean square error values, we can conclude that there is spatial variability in this criteria pollutant across the study area. This is important because it means that citizens may be exposed to more, or less, ozone than they would assume based on current regulatory monitoring.

  14. Long-term trends of surface ozone and its influencing factors at the Mt Waliguan GAW station, China – Part 2: The roles of anthropogenic emissions and climate variability

    Directory of Open Access Journals (Sweden)

    W. Xu

    2018-01-01

    summertime ozone measured at WLG shows no significant trend despite ozone increases in eastern China. Analysis of the Trajectory-mapped Ozonesonde data set for the Stratosphere and Troposphere (TOST and trajectory residence time reveals increases in direct ozone transport from the eastern sector during autumn, which adds to the autumnal ozone increase. We further examine the links of ozone variability at WLG to the quasi-biennial oscillation (QBO, the East Asian summer monsoon (EASM, and the sunspot cycle. Our results suggest that the 2–3-, 3–7-, and 11-year periodicities are linked to the QBO, EASM index, and sunspot cycle, respectively. A multivariate regression analysis is performed to quantify the relative contributions of various factors to surface ozone concentrations at WLG. Through an observational and modelling analysis, this study demonstrates the complex relationships between surface ozone at remote locations and its dynamical and chemical influencing factors.

  15. The Antarctic Ozone Hole: New Approaches for Detection of the Onset of Stratospheric Ozone Recovery

    Science.gov (United States)

    de Laat, J.; van Weele, M.; van der A, R. J.

    2016-12-01

    An important aspect of human influences on climate concerns the Antarctic ozone hole, the strong thinning of the thickness of the ozone layer during springtime over Antarctica, first observed in the early 1980s. Antarctic stratospheric ozone is expected to fully recover in the second half of the 21st century because of policy measures to eliminate emissions of ozone depleting substances. Identification of the onset of this recovery would mark an important scientific and political milestone, but has remained difficult so far owing to natural climate variability and methodological ambiguities. In this presentation, we will first give a brief introduction to methods that have been used in the past to try to identify the onset of recovery, and discuss their shortcomings and ambiguities. Secondly, we introduce and discuss a several observations-based new approaches for ozone recovery detection in the Antarctic Ozone Hole that we have developed, explain why we believe these methods are more robust than standard methods, and outline how they circumvent crucial pitfalls of the previously used methods. Finally, we present our analyses, showing that these new approaches applied to various sets of remote sensing observations provide the best evidence to date that that ozone destruction within the Antarctic Ozone Hole has significantly decreased since approximately the year 2000, and which can be attributed to concurrently decreasing ozone depleting substances.

  16. Ozone modeling

    International Nuclear Information System (INIS)

    McIllvaine, C.M.

    1994-01-01

    Exhaust gases from power plants that burn fossil fuels contain concentrations of sulfur dioxide (SO 2 ), nitric oxide (NO), particulate matter, hydrocarbon compounds and trace metals. Estimated emissions from the operation of a hypothetical 500 MW coal-fired power plant are given. Ozone is considered a secondary pollutant, since it is not emitted directly into the atmosphere but is formed from other air pollutants, specifically, nitrogen oxides (NO), and non-methane organic compounds (NMOQ) in the presence of sunlight. (NMOC are sometimes referred to as hydrocarbons, HC, or volatile organic compounds, VOC, and they may or may not include methane). Additionally, ozone formation Alternative is a function of the ratio of NMOC concentrations to NO x concentrations. A typical ozone isopleth is shown, generated with the Empirical Kinetic Modeling Approach (EKMA) option of the Environmental Protection Agency's (EPA) Ozone Isopleth Plotting Mechanism (OZIPM-4) model. Ozone isopleth diagrams, originally generated with smog chamber data, are more commonly generated with photochemical reaction mechanisms and tested against smog chamber data. The shape of the isopleth curves is a function of the region (i.e. background conditions) where ozone concentrations are simulated. The location of an ozone concentration on the isopleth diagram is defined by the ratio of NMOC and NO x coordinates of the point, known as the NMOC/NO x ratio. Results obtained by the described model are presented

  17. Temperature dependence of bromine activation due to reaction of bromide with ozone in a proxy for organic aerosols and its importance for chemistry in surface snow.

    Science.gov (United States)

    Edebeli, Jacinta; Ammann, Markus; Gilgen, Anina; Trachsel, Jürg; Avak, Sven; Eichler, Anja; Schneebeli, Martin; Bartels-Rausch, Thorsten

    2017-04-01

    Tropospheric ozone depletion events (ODEs) via halogen activation are observed in both cold and warm climates [1-3]. Very recently, it was suggested that this multiphase halogen activation chemistry dominates in the tropical and subtropical upper troposphere [4]. These occurrences beg the question of temperature dependence of halogen activation in sea-salt aerosol, which are often mixtures of sea-salt and organic molecules [3, 5]. With the application of flow-tubes, the aim of this study is to investigate the temperature dependence of bromine activation via ozone interaction in a bromide containing film as a proxy for mixed organic - sea-salt aersol. Citric acid is used in this study as a hygroscopically characterized matrix and a proxy for oxidized organics, which is of relevance to atmospheric chemistry. Here, we present reactive ozone uptake measured between 258 and 289 K. The data show high reproducibility. With available knowledge, we have reproduced the measured uptake with modelled bulk uptake while accounting for temperature dependence of the substrate's properties as diffusivity, viscosity, and gas solubility. This work is part of a cross-disciplinary project with the aim to investigate the impact of metamorphism on impurity location in aging snow and its consequences for chemical reactivity. Metamorphism drastically shapes the structure and physical properties of snow, which has impacts on heat transfer, albedo, and avalanche formation. Such changes can be driven by water vapour fluxes in dry metamorphism with a mass turnover of as much as 60% per day - much greater than previously thought [6]. The consequences for atmospheric science are a current question of research [7]. Here, we show first results of a joint experiment to probe the re-distribution of impurities during snow metamorphism in artificial snow combined with an investigation of the samples structural changes. Future work is planned with the goal to investigate to which extend the observed re

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

    Science.gov (United States)

    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.

  19. Impacto del tratamiento con ozono sobre las propiedades superficiales del carbón activado Impact of ozone treatment on activated carbon surface properties

    Directory of Open Access Journals (Sweden)

    Héctor Valdés

    2011-08-01

    Full Text Available El uso conjunto de ozono y carbón activado para tratar efluentes tóxicos ha sido demostrado recientemente. Sin embargo, existen dudas acerca del efecto del ozono sobre las propiedades del carbón activado. En este artículo se presentan resultados sobre la modificación de las propiedades superficiales de un carbón activado comercial por la acción del ozono durante diferentes tiempos de exposición. Las propiedades químicas superficiales del carbón activado fueron evaluadas utilizando las técnicas de neutralización selectiva, desorción térmica programada (DTP y el pH del punto de carga cero. Las características texturales fueron evaluadas mediante microscopía electrónica de barrido. El área superficial aparente, el volumen de microporos y mesoporos fueron obtenidos a partir de las isotermas de adsorción de nitrógeno a 77 K. Las propiedades adsortivas fueron caracterizadas por el índice de adsorción de azul de metileno. Los resultados demuestran que los grupos superficiales oxigenados presentes en el carbón activado se modifican producto del tratamiento con el ozono. A mayores dosis de ozono, el carbón sufre mayor oxidación y se incrementan los grupos ácidos en especial los grupos carboxílicos, mientras que el pH de punto de carga cero disminuye. El área BET, así como el volumen de microporos disminuyen al igual que el poder de adsorción de azul de metileno.The combined use of ozone and activated carbon has recently started to be developed for the treatment of toxic effluents. However, the effect of ozone on the properties of activated carbon is not fully elucidated. A study was undertaken of modifications of the surface properties of a commercial activated carbon produced by its ozonation during different time periods. Surface chemistry of the activated carbon samples was characterized by of selective neutralization, temperature-programmed desorption, and pH of the point of zero charge. Surface area and volume of

  20. Towards the retrieval of tropospheric ozone with the ozone monitoring instrument (OMI)

    NARCIS (Netherlands)

    Mielonen, T.; De Haan, J.F.; Van Peet, J.C.A.; Eremenko, M.; Veefkind, J.P.

    2015-01-01

    We have assessed the sensitivity of the operational Ozone Monitoring Instrument (OMI) ozone profile retrieval algorithm to a number of a priori and radiative transfer assumptions. We studied the effect of stray light correction, surface albedo assumptions and a priori ozone profiles on the retrieved

  1. Chemical and climatic drivers of radiative forcing due to changes in stratospheric and tropospheric ozone over the 21st century

    Directory of Open Access Journals (Sweden)

    A. Banerjee

    2018-02-01

    Full Text Available The ozone radiative forcings (RFs resulting from projected changes in climate, ozone-depleting substances (ODSs, non-methane ozone precursor emissions and methane between the years 2000 and 2100 are calculated using simulations from the UM-UKCA chemistry–climate model (UK Met Office's Unified Model containing the United Kingdom Chemistry and Aerosols sub-model. Projected measures to improve air-quality through reductions in non-methane tropospheric ozone precursor emissions present a co-benefit for climate, with a net global mean ozone RF of −0.09 W m−2. This is opposed by a positive ozone RF of 0.05 W m−2 due to future decreases in ODSs, which is driven by an increase in tropospheric ozone through stratosphere-to-troposphere transport of air containing higher ozone amounts. An increase in methane abundance by more than a factor of 2 (as projected by the RCP8.5 scenario is found to drive an ozone RF of 0.18 W m−2, which would greatly outweigh the climate benefits of non-methane tropospheric ozone precursor reductions. A small fraction (∼ 15 % of the ozone RF due to the projected increase in methane results from increases in stratospheric ozone. The sign of the ozone RF due to future changes in climate (including the radiative effects of greenhouse gases, sea surface temperatures and sea ice changes is shown to be dependent on the greenhouse gas emissions pathway, with a positive RF (0.05 W m−2 for RCP4.5 and a negative RF (−0.07 W m−2 for the RCP8.5 scenario. This dependence arises mainly from differences in the contribution to RF from stratospheric ozone changes. Considering the increases in tropopause height under climate change causes only small differences (≤ |0.02| W m−2 for the stratospheric, tropospheric and whole-atmosphere RFs.

  2. Optical remote measurement of ozone in cirrus clouds; Optische Fernmessung von Ozon in Zirruswolken

    Energy Technology Data Exchange (ETDEWEB)

    Reichardt, J. [GKSS-Forschungszentrum Geesthacht GmbH (Germany). Inst. fuer Physikalische und Chemische Analytik

    1998-12-31

    The subject of this thesis is theoretical and experimental investigations into the simultaneous optical remote measurement of atmospheric ozone concentration and particle properties. A lidar system was developed that combines the Raman-lidar and the polarization-lidar with the Raman-DIAL technique. An error analysis is given for ozone measurements in clouds. It turns out that the wavelength dependencies of photon multiple scattering and of the particle extinction coefficient necessitate a correction of the measured ozone concentration. To quantify the cloud influence, model calculations based on particle size distributions of spheres are carried out. The most important experimental result of this thesis is the measured evidence of pronounced minima in the ozone distribution in a humid upper troposphere shortly before and during cirrus observation. Good correlation between ozone-depleted altitude ranges and ice clouds is found. This finding is in contrast to ozone profiles measured in a dry and cloud-free troposphere. (orig.) 151 refs.

  3. Sources of reactive bromine in polar regions and its implications for ozone in the troposphere

    Science.gov (United States)

    Griffiths, Paul; Archibald, Alex; Yang, Xin; Pyle, John

    2014-05-01

    In the last two decades, significant depletion of boundary layer ozone (ozone depletion events, ODEs) has been observed in both Arctic and Antarctic spring. ODEs are attributed to catalytic destruction by bromine radicals (Br plus BrO), especially during bromine explosion events, when high concentrations of BrO periodically occur. The source of bromine and the mechanism that sustains the high BrO levels are still the subject of study, and there remains scope for improving our understanding of reactive bromine budgets in polar regions. Yang et al. (2008) suggested snow could provide a source of (depleted) sea-salt aerosol if blown from the surface of ice, while recent work by Pratt et al. (2013) posits Br2 production within saline snow and sea ice. In this poster, we consider the production of sea-salt aerosol from a mixture of snow and sea ice during periods of strong wind. We use a combination of box models and the United Kingdom Chemistry and Aerosols scheme, run as a component of the UK Met Office Unified Model, to quantify the effect of bromine release in the boundary layer and its effect on ozone at the regional scale. The importance of heterogeneous reactions is quantified and new data from the recent Polarstern cruise by members of the British Antarctic Survey as part of the NERC-funded BLOWSEA project will be considered.

  4. Impact of the 2008 Global Recession on air quality over the United States: Implications for surface ozone levels from changes in NOx emissions

    Science.gov (United States)

    Tong, Daniel; Pan, Li; Chen, Weiwei; Lamsal, Lok; Lee, Pius; Tang, Youhua; Kim, Hyuncheol; Kondragunta, Shobha; Stajner, Ivanka

    2016-09-01

    Satellite and ground observations detected large variability in nitrogen oxides (NOx) during the 2008 economic recession, but the impact of the recession on air quality has not been quantified. This study combines observed NOx trends and a regional chemical transport model to quantify the impact of the recession on surface ozone (O3) levels over the continental United States. The impact is quantified by simulating O3 concentrations under two emission scenarios: business-as-usual (BAU) and recession. In the BAU case, the emission projection from the Cross-State Air Pollution Rule is used to estimate the "would-be" NOx emission level in 2011. In the recession case, the actual NO2 trends observed from Air Quality System ground monitors and the Ozone Monitoring Instrument on the Aura satellite are used to obtain "realistic" changes in NOx emissions. The model prediction with the recession effect agrees better with ground O3 observations over time and space than the prediction with the BAU emission. The results show that the recession caused a 1-2 ppbv decrease in surface O3 concentration over the eastern United States, a slight increase (0.5-1 ppbv) over the Rocky Mountain region, and mixed changes in the Pacific West. The gain in air quality benefits during the recession, however, could be quickly offset by the much slower emission reduction rate during the post-recession period.

  5. Impact of the 2008 Global Recession on Air Quality over the United States: Implications for Surface Ozone Levels from Changes in NOx Emissions

    Science.gov (United States)

    Tong, Daniel; Pan, Li; Chen, Weiwei; Lamsal, Lok; Lee, Pius; Tang, Youhua; Kim, Hyuncheol; Kondragunta, Shobha; Stajner, Ivanka

    2016-01-01

    Satellite and ground observations detected large variability in nitrogen oxides (NOx) during the 2008 economic recession, but the impact of the recession on air quality has not been quantified. This study combines observed NOx trends and a regional chemical transport model to quantify the impact of the recession on surface ozone (O3) levels over the continental United States. The impact is quantified by simulating O3 concentrations under two emission scenarios: business-as-usual (BAU) and recession. In the BAU case, the emission projection from the Cross-State Air Pollution Rule is used to estimate the would-be NOx emission level in 2011. In the recession case, the actual NO2 trends observed from Air Quality System ground monitors and the Ozone Monitoring Instrument on the Aura satellite are used to obtain realistic changes in NOx emissions. The model prediction with the recession effect agrees better with ground O3 observations over time and space than the prediction with the BAU emission. The results show that the recession caused a 12ppbv decrease in surface O3 concentration over the eastern United States, a slight increase (0.51ppbv) over the Rocky Mountain region, and mixed changes in the Pacific West. The gain in air quality benefits during the recession, however, could be quickly offset by the much slower emission reduction rate during the post-recession period.

  6. Nitrous Oxides Ozone Destructiveness Under Different Climate Scenarios

    Science.gov (United States)

    Kanter, David R.; McDermid, Sonali P.

    2016-01-01

    Nitrous oxide (N2O) is an important greenhouse gas and ozone depleting substance as well as a key component of the nitrogen cascade. While emissions scenarios indicating the range of N2O's potential future contributions to radiative forcing are widely available, the impact of these emissions scenarios on future stratospheric ozone depletion is less clear. This is because N2O's ozone destructiveness is partially dependent on tropospheric warming, which affects ozone depletion rates in the stratosphere. Consequently, in order to understand the possible range of stratospheric ozone depletion that N2O could cause over the 21st century, it is important to decouple the greenhouse gas emissions scenarios and compare different emissions trajectories for individual substances (e.g. business-as-usual carbon dioxide (CO2) emissions versus low emissions of N2O). This study is the first to follow such an approach, running a series of experiments using the NASA Goddard Institute for Space Sciences ModelE2 atmospheric sub-model. We anticipate our results to show that stratospheric ozone depletion will be highest in a scenario where CO2 emissions reductions are prioritized over N2O reductions, as this would constrain ozone recovery while doing little to limit stratospheric NOx levels (the breakdown product of N2O that destroys stratospheric ozone). This could not only delay the recovery of the stratospheric ozone layer, but might also prevent a return to pre-1980 global average ozone concentrations, a key goal of the international ozone regime. Accordingly, we think this will highlight the importance of reducing emissions of all major greenhouse gas emissions, including N2O, and not just a singular policy focus on CO2.

  7. Evaluating a Space-Based Indicator of Surface Ozone-NOx-VOC Sensitivity Over Midlatitude Source Regions and Application to Decadal Trends

    Science.gov (United States)

    Jin, Xiaomeng; Fiore, Arlene M.; Murray, Lee T.; Valin, Lukas C.; Lamsal, Lok N.; Duncan, Bryan; Folkert Boersma, K.; De Smedt, Isabelle; Abad, Gonzalo Gonzalez; Chance, Kelly; Tonnesen, Gail S.

    2017-10-01

    Determining effective strategies for mitigating surface ozone (O3) pollution requires knowledge of the relative ambient concentrations of its precursors, NOx, and VOCs. The space-based tropospheric column ratio of formaldehyde to NO2 (FNR) has been used as an indicator to identify NOx-limited versus NOx-saturated O3 formation regimes. Quantitative use of this indicator ratio is subject to three major uncertainties: (1) the split between NOx-limited and NOx-saturated conditions may shift in space and time, (2) the ratio of the vertically integrated column may not represent the near-surface environment, and (3) satellite products contain errors. We use the GEOS-Chem global chemical transport model to evaluate the quantitative utility of FNR observed from the Ozone Monitoring Instrument over three northern midlatitude source regions. We find that FNR in the model surface layer is a robust predictor of the simulated near-surface O3 production regime. Extending this surface-based predictor to a column-based FNR requires accounting for differences in the HCHO and NO2 vertical profiles. We compare four combinations of two OMI HCHO and NO2 retrievals with modeled FNR. The spatial and temporal correlations between the modeled and satellite-derived FNR vary with the choice of NO2 product, while the mean offset depends on the choice of HCHO product. Space-based FNR indicates that the spring transition to NOx-limited regimes has shifted at least a month earlier over major cities (e.g., New York, London, and Seoul) between 2005 and 2015. This increase in NOx sensitivity implies that NOx emission controls will improve O3 air quality more now than it would have a decade ago.

  8. Ozone Pollution

    Science.gov (United States)

    Known as tropospheric or ground-level ozone, this gas is harmful to human heath and the environment. Since it forms from emissions of volatile organic compounds (VOCs) and nitrogen oxides (NOx), these pollutants are regulated under air quality standards.

  9. Defense meteorological satellite measurements of total ozone

    International Nuclear Information System (INIS)

    Lovill, J.E.; Ellis, J.S.; Luther, F.M.; Sullivan, R.J.; Weichel, R.L.

    1992-01-01

    A multichannel filter radiometer (MFR) on Defense Meteorological Satellites (DMS) that measured total ozone on a global-scale from March 1977 - February 1980 is described. The total ozone data measured by the MFR were compared with total ozone data taken by surfaced-based Dobson spectrophotometers. When comparisons were made for five months, the Dobson spectrophotometer measured 2-5% more total ozone than the MFR. Comparisons between the Dobson spectrophotometer and the MFR showed a reduced RMS difference as the comparisons were made at closer proximity. A Northern Hemisphere total ozone distribution obtained from MFR data is presented

  10. Impacts of ozone on trees and crops

    International Nuclear Information System (INIS)

    Felzer, B.S.; Cronina, T.; Melillo, J.M.; Reilly, J.M.; Xiaodong, Wang

    2007-01-01

    In this review article, we explore how surface-level ozone affects trees and crops with special emphasis on consequences for productivity and carbon sequestration. Vegetation exposure to ozone reduces photosynthesis, growth, and other plant functions. Ozone formation in the atmosphere is a product of NO x , which are also a source of nitrogen deposition. Reduced carbon sequestration of temperate forests resulting from ozone is likely offset by increased carbon sequestration from nitrogen fertilization. However, since fertilized crop-lands are generally not nitrogen-limited, capping ozone-polluting substances in the USA, Europe, and China can reduce future crop yield loss substantially. (authors)

  11. The effect of SST emissions on the earth's ozone layer

    Science.gov (United States)

    Whitten, R. C.; Turco, R. P.

    1974-01-01

    The work presented here is directed toward assessment of environmental effects of the supersonic transport (SST). The model used for the purpose includes vertical eddy transport and the photochemistry of the O-H-N system. It is found that the flight altitude has a pronounced effect on ozone depletion. The largest ozone reduction occurs for NO deposition above an altitude of 20 km.

  12. The ozone hole and the 1995 Nobel prize in chemistry

    International Nuclear Information System (INIS)

    Berger, A.

    1996-01-01

    To mark to award of the 1995 Nobel Prize in chemistry to three world renowned atmospheric chemists, this paper recalls the history of scientific progress in stratospheric ozone chemistry. Then it summarizes current knowledge of ozone-layer depletion and its impact on climate, vegetation and human health. (author). 21 refs., 12 figs

  13. Temperature Trends in the Tropical Upper Troposphere and Lower Stratosphere: Connections with Sea Surface Temperatures and Implications for Water Vapor and Ozone

    Science.gov (United States)

    Garfinkel, C. I.; Waugh, D. W.; Oman, L. D.; Wang, L.; Hurwitz, M. M.

    2013-01-01

    Satellite observations and chemistry-climate model experiments are used to understand the zonal structure of tropical lower stratospheric temperature, water vapor, and ozone trends. The warming in the tropical upper troposphere over the past 30 years is strongest near the Indo-Pacific warm pool, while the warming trend in the western and central Pacific is much weaker. In the lower stratosphere, these trends are reversed: the historical cooling trend is strongest over the Indo-Pacific warm pool and is weakest in the western and central Pacific. These zonal variations are stronger than the zonal-mean response in boreal winter. Targeted experiments with a chemistry-climate model are used to demonstrate that sea surface temperature (hereafter SST) trends are driving the zonal asymmetry in upper tropospheric and lower stratospheric tropical temperature trends. Warming SSTs in the Indian Ocean and in the warm pool region have led to enhanced moist heating in the upper troposphere, and in turn to a Gill-like response that extends into the lower stratosphere. The anomalous circulation has led to zonal structure in the ozone and water vapor trends near the tropopause, and subsequently to less water vapor entering the stratosphere. The radiative impact of these changes in trace gases is smaller than the direct impact of the moist heating. Projected future SSTs appear to drive a temperature and water vapor response whose zonal structure is similar to the historical response. In the lower stratosphere, the changes in water vapor and temperature due to projected future SSTs are of similar strength to, though slightly weaker than, that due directly to projected future CO2, ozone, and methane.

  14. The ozone hole and the 1995 Nobel prize in chemistry; Trou d`ozone et Prix Nobel 1995 de chimie

    Energy Technology Data Exchange (ETDEWEB)

    Berger, A. [Universite Catholique de Louvain (UCL), Louvain-la-Neuve (Belgium). Inst. d`Astronomie et de Geophysique G. Lemaitre

    1996-03-01

    To mark to award of the 1995 Nobel Prize in chemistry to three world renowned atmospheric chemists, this paper recalls the history of scientific progress in stratospheric ozone chemistry. Then it summarizes current knowledge of ozone-layer depletion and its impact on climate, vegetation and human health. (author). 21 refs., 12 figs.

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

    OpenAIRE

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

    2009-01-01

    Ozone depletion by chlorofluorocarbons (CFCs) was first proposed by Molina and Rowland in their 1974 Nature paper. Since that time, the scientific connection between ozone losses and CFCs and other ozone depleting substances (ODSs) has been firmly established with laboratory measurements, atmospheric observations, and modeling research. This science research led to the implementation of international agreements that largely stopped the production of ODSs. In this study we use a fully-c...

  16. Identification of ozonation by-products of 4- and 5-methyl-1H-benzotriazole during the treatment of surface water to drinking water.

    Science.gov (United States)

    Müller, Alexander; Weiss, Stefan C; Beisswenger, Judith; Leukhardt, H Georg; Schulz, Wolfgang; Seitz, Wolfram; Ruck, Wolfgang K L; Weber, Walter H

    2012-03-01

    During the treatment of surface water to drinking water, ozonation is often used for disinfection and to remove organic trace substances, whereby oxidation by-products can be formed. Here we use the example of tolyltriazole to describe an approach for identifying relevant oxidation by-products in the laboratory and subsequently detecting them in an industrial-scale process. The identification process involves ozonation experiments with pure substances at laboratory level (concentration range mg L(-1)). The reaction solutions from different ozone contact times were analyzed by high performance liquid chromatography - quadrupole time-of-flight mass spectrometry (HPLC-QTOF-MS) in full scan mode. Various approaches were used to detect the oxidation by-products: (i) target searches of postulated oxidation by-products, (ii) comparisons of chromatograms (e.g., UV/VIS) of the different samples, and (iii) color-coded abundance time courses (kinetic) of all detected compounds were illustrated in a kind of a heat map. MS/MS, H/D exchange, and derivatization experiments were used for structure elucidation for the detected by-product. Due to the low contaminant concentrations (ng L(-1)-range) of contaminants in the untreated water, the conversion of results from laboratory experiments to an industrial-scale required the use of HPLC-MS/MS with sample enrichment (e.g., solid phase extraction.) In cases where reference substances were not available or oxidation by-products without clear structures were detected, reaction solutions from laboratory experiments were used to optimize the analytical method to detect ng L(-1) in the samples of the industrial processes. We exemplarily demonstrated the effectiveness of the methodology with the industrial chemicals 4- and 5-methyl-1H-benzotriazole (4- and 5-MBT) as an example. Moreover, not only did we identify several oxidation by-products in the laboratory experiments tentatively, but also detected three of the eleven reaction

  17. Optimization of Catalytic Ozonation Process for Formaldehyde Mineralization from Synthetic Wastewater by Fe/MgO Nanoparticles Synthesis by Sol-Gel Method by Response Surface Model

    Directory of Open Access Journals (Sweden)

    Ghorban Asgari

    2014-09-01

    Full Text Available Background: Design experiment stages of formalin mineralization process by center composition design (CCD cause ease of work, reducing the number of samples, increasing the accuracy of optimized conditions and the interaction parameters determined during the process. The aim of this study was optimization of catalytic ozonation process for formaldehyde mineralization from synthetic wastewater by Fe/MgO nanoparticles synthesis by sol-gel method by response surface model. Methods: This experimental study was conducted in a semi-batch reactor, using a RSM by taking 3 factors in the final stage of pH (7-9, reaction time (10-20 min and catalyst dose (1.1-1.3 g/L was investigated. Synthesis of nanoparticles was done by sol-gel method. The results were analyzed by Design Expert 7.0.1 software. Results: The results showed that the process was dependent on the parameters studied and changing each parameter, affected the process efficiency and other parameters. The optimum conditions predicted for the process was 86.51% of mineralization efficiency. Optimum condition included pH=8.82, reaction time of 20 minute and catalyst dose of 1.3 g/L. The correlation coefficient for the process was determined 0.91. Conclusion: Using a statistical model could reduce the number of experiments, the accuracy and the prediction process. The catalytic ozonation process has the ability to remove formaldehyde with high efficiency and the process was environmental friendly.

  18. Stratospheric Ozone Response in Experiments G3 and G4 of the Geoengineering Model Intercomparison Project (GeoMIP)

    Science.gov (United States)

    Pitari, Giovanni; Aquila, Valentina; Kravitz, Ben; Watanabe, Shingo; Tilmes, Simone; Mancini, Eva; DeLuca, Natalia; DiGenova, Glauco

    2013-01-01

    Geoengineering with stratospheric sulfate aerosols has been proposed as a means of temporarily cooling the planet, alleviating some of the side effects of anthropogenic CO2 emissions. However, one of the known side effects of stratospheric injections of sulfate aerosols is a decrease in stratospheric ozone. Here we show results from two general circulation models and two coupled chemistry climate models that have simulated stratospheric sulfate aerosol geoengineering as part of the Geoengineering Model Intercomparison Project (GeoMIP). Changes in photolysis rates and upwelling of ozone-poor air in the tropics reduce stratospheric ozone, suppression of the NOx cycle increases stratospheric ozone, and an increase in available surfaces for heterogeneous chemistry modulates reductions in ozone. On average, the models show a factor 20-40 increase of the sulfate aerosol surface area density (SAD) at 50 hPa in the tropics with respect to unperturbed background conditions and a factor 3-10 increase at mid-high latitudes. The net effect for a tropical injection rate of 5 Tg SO2 per year is a decrease in globally averaged ozone by 1.1-2.1 DU in the years 2040-2050 for three models which include heterogeneous chemistry on the sulfate aerosol surfaces. GISS-E2-R, a fully coupled general circulation model, performed simulations with no heterogeneous chemistry and a smaller aerosol size; it showed a decrease in ozone by 9.7 DU. After the year 2050, suppression of the NOx cycle becomes more important than destruction of ozone by ClOx, causing an increase in total stratospheric ozone. Contribution of ozone changes in this experiment to radiative forcing is 0.23 W m-2 in GISS-E2-R and less than 0.1 W m-2 in the other three models. Polar ozone depletion, due to enhanced formation of both sulfate aerosol SAD and polar stratospheric clouds, results in an average 5 percent increase in calculated surface UV-B.

  19. Sensitivity Modeling Study for an Ozone Occurrence during the 1996 Paso Del Norte Ozone Campaign

    Directory of Open Access Journals (Sweden)

    Duanjun Lu

    2008-11-01

    Full Text Available Surface ozone pollution has been a persistent environmental problem in the US and Europe as well as the developing countries. A key prerequisite to find effective alternatives to meeting an ozone air quality standard is to understand the importance of local anthropogenic emissions, the significance of biogenic emissions, and the contribution of long-range transport. In this study, an air quality modeling system that includes chemistry and transport, CMAQ, an emission processing model, SMOKE, and a mesoscale numerical meteorological model, WRF, has been applied to investigate an ozone event occurring during the period of the 1996 Paso del Norte Ozone Campaign. The results show that the modeling system exhibits the capability to simulate this high ozone occurrence by providing a comparable temporal variation of surface ozone concentration at one station and to capture the spatial evolution of the event. Several sensitivity tests were also conducted to identify the contributions to high surface ozone concentration from eight VOC subspecies, biogenic VOCs, anthropogenic VOCs and long-range transportation of ozone and its precursors. It is found that the reductions of ETH, ISOP, PAR, OLE and FORM help to mitigate the surface ozone concentration, and like anthropogenic VOCs, biogenic VOC plays a nonnegligible role in ozone formation. But for this case, long-range transport of ozone and its precursors appears to produce an insignificant contribution.

  20. Sensitivity modeling study for an ozone occurrence during the 1996 Paso Del Norte Ozone Campaign.

    Science.gov (United States)

    Lu, Duanjun; Reddy, Remata S; Fitzgerald, Rosa; Stockwell, William R; Williams, Quinton L; Tchounwou, Paul B

    2008-12-01

    Surface ozone pollution has been a persistent environmental problem in the US and Europe as well as the developing countries. A key prerequisite to find effective alternatives to meeting an ozone air quality standard is to understand the importance of local anthropogenic emissions, the significance of biogenic emissions, and the contribution of long-range transport. In this study, an air quality modeling system that includes chemistry and transport, CMAQ, an emission processing model, SMOKE, and a mesoscale numerical meteorological model, WRF, has been applied to investigate an ozone event occurring during the period of the 1996 Paso del Norte Ozone Campaign. The results show that the modeling system exhibits the capability to simulate this high ozone occurrence by providing a comparable temporal variation of surface ozone concentration at one station and to capture the spatial evolution of the event. Several sensitivity tests were also conducted to identify the contributions to high surface ozone concentration from eight VOC subspecies, biogenic VOCs, anthropogenic VOCs and long-range transportation of ozone and its precursors. It is found that the reductions of ETH, ISOP, PAR, OLE and FORM help to mitigate the surface ozone concentration, and like anthropogenic VOCs, biogenic VOC plays a nonnegligible role in ozone formation. But for this case, long-range transport of ozone and its precursors appears to produce an insignificant contribution.

  1. Eight years of stratospheric ozone observations at Marambio, Antarctica

    Energy Technology Data Exchange (ETDEWEB)

    Damski, J.; Taalas, P. [Finnish Meteorological Inst., Helsinki (Finland). Section of Ozone and UV Research

    1995-12-31

    In this work behaviour of the stratospheric ozone using the total ozone and ozone sounding measurements from Marambio (64 deg 14`S, 56 deg 37`W) at Antarctic Peninsula has been studied. The effects of depleted stratospheric ozone to the UV-B-radiation are investigated employing a radiative transfer model, and the Marambio total ozone measurements. The levels of UV-B radiation have been studied from the point of the erythemal UV-B-doses on the horizontal human epidermis. The low values of total ozone at Marambio are also reflected to the received UV-doses which have increased roughly 20-80% (compared to long term average) during austral spring and summer. In respective to the total amount of ozone, the model calculations show that during October the UV-B-doses can be at the same level they should be during normal summer

  2. Emergence of healing in the Antarctic ozone layer.

    Science.gov (United States)

    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.

  3. Emergence of healing in the Antarctic ozone layer

    Science.gov (United States)

    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.

  4. Thinning of the ozone layer: Facts and consequences

    Energy Technology Data Exchange (ETDEWEB)

    Coldiron, B.M. (Univ. of Illinois, Chicago (United States))

    1992-11-01

    The ozone layer is showing small but definite signs of depletion. Despite this, significantly increased UV radiation transmission at ground level has been found only in the Antarctic and Arctic regions. The potential for increased transmission of UV radiation will exist for the next several hundred years. Although little damage from increased UV radiation has occurred so far, the potential for long-term problems is great. The natural history of ozone and the causes and consequences of, and possible solutions to ozone depletion are examined in this article. 36 refs.

  5. Ozone Reductions Using Residential Building Envelopes

    Energy Technology Data Exchange (ETDEWEB)

    Walker, Iain S.; Sherman, Max; Nazaroff, William W.

    2009-02-01

    Ozone is an air pollutant with that can have significant health effects and a significant source of ozone in some regions of California is outdoor air. Because people spend the vast majority of their time indoors, reduction in indoor levels of ozone could lead to improved health for many California residents. Ozone is removed from indoor air by surface reactions and can also be filtered by building envelopes. The magnitude of the envelope impact depends on the specific building materials that the air flows over and the geometry of the air flow paths through the envelope that can be changes by mechanical ventilation operation. The 2008 Residential Building Standards in California include minimum requirements for mechanical ventilation by referencing ASHRAE Standard 62.2. This study examines the changes in indoor ozone depending on the mechanical ventilation system selected to meet these requirements. This study used detailed simulations of ventilation in a house to examine the impacts of different ventilation systems on indoor ozone concentrations. The simulation results showed that staying indoors reduces exposure to ozone by 80percent to 90percent, that exhaust ventilation systems lead to lower indoor ozone concentrations, that opening of windows should be avoided at times of high outdoor ozone, and that changing the time at which mechanical ventilation occurs has the ability to halve exposure to ozone. Future work should focus on the products of ozone reactions in the building envelope and the fate of these products with respect to indoor exposures.

  6. La destruction de la couche d'ozone et ses implications en Région wallonne

    OpenAIRE

    Mahieu, Emmanuel

    2007-01-01

    Stratospheric ozone is an important constituent of the Earth's atmosphere since it protects the biosphere from the most harmful ultraviolet radiations emitted by the sun. Some human activiites such as the use of man-mande chlorofluorocarbons have resulted in major destruction of ozone, in particular in the polar regions of the stratosphere. The Montreal Protocol has been successful in limiting the emissions of ozone depleting substances such as the complete ozone recovery is expected to take ...

  7. Model Calculations of Changes in Tropospheric Ozone Over Europe and the Role of Surface Sources and Aircraft Emissions

    Energy Technology Data Exchange (ETDEWEB)

    Hov, Oe. [Bergen Univ. (Norway)

    1996-01-01

    This conference paper deals with a study of the impact of various sources of NO{sub x} on the ozone production in the free troposphere. A comprehensive two-dimensional zonally averaged chemistry/transport model and a three-dimensional meso-scale chemical transport (MCT) model are used in the study. Using the two-dimensional model, three surches of NO{sub x} in the upper troposphere were examined covering NO{sub x} produced by lightening, NO{sub x} (and NO{sub y}) brought to the upper troposphere from the planetary boundary layer by rapid vertical transport processes, and NO{sub x} emitted from aircraft. 4 refs.

  8. Dobson spectrophotometer ozone measurements during international ozone rocketsonde intercomparison

    Science.gov (United States)

    Parsons, C. L.

    1980-01-01

    Measurements of the total ozone content of the atmosphere, made with seven ground based instruments at a site near Wallops Island, Virginia, are discussed in terms for serving as control values with which the rocketborne sensor data products can be compared. These products are profiles of O3 concentration with altitude. By integrating over the range of altitudes from the surface to the rocket apogee and by appropriately estimating the residual ozone amount from apogee to the top of the atmosphere, a total ozone amount can be computed from the profiles that can be directly compared with the ground based instrumentation results. Dobson spectrophotometers were used for two of the ground-based instruments. Preliminary data collected during the IORI from Dobson spectrophotometers 72 and 38 are presented. The agreement between the two and the variability of total ozone overburden through the experiment period are discussed.

  9. Heterogeneous nano-Fe/Ca/CaO catalytic ozonation for selective surface hydrophilization of plastics containing brominated and chlorinated flame retardants (B/CFRs): separation from automobile shredder residue by froth flotation.

    Science.gov (United States)

    Mallampati, Srinivasa Reddy; Lee, Byoung Ho; Mitoma, Yoshiharu; Simion, Cristian

    2017-02-01

    One method of weakening the inherently hydrophobic surface of plastics relevant to flotation separation is heterogeneous nano-Fe/Ca/CaO catalytic ozonation. Nano-Fe/Ca/CaO-catalyzed ozonation for 15 min efficiently decreases the surface hydrophobicity of brominated and chlorinated flame retardant (B/CFR)-containing plastics (such as acrylonitrile-butadienestyrene (ABS), high-impact polystyrene (HIPS), and polyvinyl chloride (PVC)) in automobile shredder residue (ASR) to such an extent that their flotation ability is entirely depressed. Such a hydrophilization treatment also stimulates the ABS, HIPS, and PVC surface roughness, wetting of the surface, and the thermodynamic equilibrium conditions at the surface and ultimately changes surface polarity. SEM-EDS, AFM, and XPS analyses of the PVC and ABS surfaces demonstrated a marked decrease in [Cl/Br] and a significant increase in the number of hydrophilic groups, such as C-O, C=O, and (C=O)-O. Under froth flotation conditions at 50 rpm, about 99.5 % of ABS and 99.5 % of HIPS in ASR samples settled out, resulting in a purity of 98 and 98.5 % for ABS and HIPS in ASR samples, respectively. Furthermore, at 150 rpm, we also obtained 100 % PVC separation in the settled fraction, with 98 % purity in ASR. Total recovery of non-B/CFR-containing plastics reached nearly 100 % in the floating fraction. The amount of nano-Fe/Ca/CaO reagent employed during ozonation is very small, and additional removal of surface contaminants from the recycled ASR plastic surfaces by ozonation makes the developed process simpler, greener, and more effective.

  10. Substitution of R502 in existing refrigerating, air-conditioning and heat pump systems with refrigerants of low ozone depletion potential in the Federal Republic of Germany; Ersatz von R 502 in bestehenden Kaelte-, Klima- und Waermepumpenanlagen in der Bundesrepublik Deutschland durch Kaeltemittel mit geringerem Ozonabbaupotential

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-06-01

    The technical basics and the state of engineering for the substitution of R502 in existing refrigeration systems are described and explained. The report contains an overview of the current applications of R502 in the FRG, the presentation and discussion of existing substitutes, the presentation and valuations of research and experiences with the adaptation to alternative refrigerants, the presentation of the required infrastructure and a discussion of the technical feasibility. The conversion of existing systems to refrigerants of lower ozone depletion potential is in conclusion valuated with regard to its technical feasibility, environmental relevance and economic efficiency. (orig.) [Deutsch] Es werden die technischen Grundlagen und der Stand der Technik zum Ersatz von R502 in bestehenden Kaelteanlagen dargestellt und erlaeutert. Der Bericht beinhaltet einen Ueberblick ueber die derzeitige Anwendung von R502 in der BRD, die Vorstellung und Diskussion existierender Ersatzstoffe, die Darstellung und Bewertung der Forschung und Erfahrungen zu Umruestungen auf Ersatzstoffe, die Vorstellung der erforderlichen Infrastruktur und die Diskussion der technischen Durchfuehrbarkeit. Die Umstellung bestehender Anlagen auf Kaeltemittel mit geringerem Ozonabbaupotential wird abschliessend hinsichtlich der technischen Durchfuehrbarkeit, der Umweltrelevanz und der Wirtschaftlichkeit bewertet. (orig.)

  11. Ozone decay in chemical reactor for ozone-dynamical disintegration of used tyres

    International Nuclear Information System (INIS)

    Golota, V.I.; Manuilenko, O.V.; Taran, G.V.; Dotsenko, Yu.V.; Pismenetskii, A.S.; Zamuriev, A.A.; Benitskaja, V.A.

    2011-01-01

    The ozone decay kinetics in the chemical reactor intended for used tyres disintegration is investigated experimentally and theoretically. Ozone was synthesized in barrierless ozonizers based on the streamer discharge. The chemical reactor for tyres disintegration in the ozone-air environment represents the cylindrical chamber, which feeds from the ozonizer by ozone-air mixture with the specified rate of volume flow, and with known ozone concentration. The output of the used mixture, which rate of volume flow is also known, is carried out through the ozone destructor. As a result of ozone decay in the volume and on the reactor walls, and output of the used mixture from the reactor, the ozone concentration in the reactor depends from time. In the paper, the analytical expression for dependence of ozone concentration in the reactor from time and from the parameters of a problem such as the volumetric feed rate, ozone concentration on the input in the reactor, volume flow rate of the used mixture, the volume of the reactor and the area of its internal surface is obtained. It is shown that experimental results coincide with good accuracy with analytical ones.

  12. Low modeled ozone production suggests underestimation of precursor emissions (especially NOx) in Europe

    OpenAIRE

    Oikonomakis, Emmanouil; Aksoyoglu, Sebnem; Ciarelli, Giancarlo; Baltensperger, Urs; Prévôt, André Stephan Henry

    2018-01-01

    High surface ozone concentrations, which usually occur when photochemical ozone production takes place, pose a great risk to human health and vegetation. Air quality models are often used by policy makers as tools for the development of ozone mitigation strategies. However, the modeled ozone production is often not or not enough evaluated in many ozone modeling studies. The focus of this work is to evaluate the modeled ozone production in Europe indirectly, with the use of t...

  13. The Antarctic Ozone Hole

    Science.gov (United States)

    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…

  14. Physics of Fresh Produce Safety: Role of Diffusion and Tissue Reaction in Sanitization of Leafy Green Vegetables with Liquid and Gaseous Ozone-Based Sanitizers.

    Science.gov (United States)

    Shynkaryk, Mykola V; Pyatkovskyy, Taras; Mohamed, Hussein M; Yousef, Ahmed E; Sastry, Sudhir K

    2015-12-01

    Produce safety has received much recent attention, with the emphasis being largely on discovery of how microbes invade produce. However, the sanitization operation deserves more attention than it has received. The ability of a sanitizer to reach the site of pathogens is a fundamental prerequisite for efficacy. This work addresses the transport processes of ozone (gaseous and liquid) sanitizer for decontamination of leafy greens. The liquid sanitizer was ineffective against Escherichia coli K-12 in situations where air bubbles may be trapped within cavities. A model was developed for diffusion of sanitizer into the interior of produce. The reaction rate of ozone with the surface of a lettuce leaf was determined experimentally and was used in a numerical simulation to evaluate ozone concentrations within the produce and to determine the time required to reach different locations. For aqueous ozone, the penetration depth was limited to several millimeters by ozone self-decomposition due to the significant time required for diffusion. In contrast, gaseous sanitizer was able to reach a depth of 100 mm in several minutes without depletion in the absence of reaction with surfaces. However, when the ozone gas reacted with the produce surface, gas concentration was significantly affected. Simulation data were validated experimentally by measuring ozone concentrations at the bottom of a cylinder made of lettuce leaf. The microbiological test confirmed the relationship between ozone transport, its self-decomposition, reaction with surrounding materials, and the degree of inactivation of E. coli K-12. Our study shows that decontamination of fresh produce, through direct contact with the sanitizer, is more feasible with gaseous than with aqueous sanitizers. Therefore, sanitization during a high-speed washing process is effective only for decontaminating the wash water.

  15. Ozone Effect On the Properties of Aramid Fabric

    Directory of Open Access Journals (Sweden)

    Wang Yan

    2017-06-01

    Full Text Available The limitation of aramid fiber is its surface property, which results in its very poor interfacial adhesion to most of commercial resins. In order to improve the surface property of the aramid fiber, ozone treatment was carried out in this work. The aramid fabrics were evaluated in terms of surface morphology, wicking effect, tensile property, and ball bursting test. The results showed that the surface morphology of aramid fabrics did not undergo an obvious change; the wicking effect increased slightly with an increase in ozone treatment time; the tenacity and elongation of aramid fibers and fabrics did not significant change after ozone treatment, but the tenacity and elongation of aramid yarns showed significant improvement after ozone treatment, and increased with the increase of ozone treatment time; the ball bursting load and penetration displacement had a slight increase as well after ozone treatment. Therefore, ozone treatment could be one method to improve the surface property of the aramid fiber.

  16. Effects of argon sputtering and UV-ozone radiation on the physico-chemical surface properties of ITO

    Science.gov (United States)

    Che, Hui; El Bouanani, M.

    2018-01-01

    X-ray photoelectron spectroscopy (XPS) and Ultraviolet Photoelectron Spectroscopy (UPS) were used to evaluate and determine the effects of 1 KeV Ar+ irradiation (sputtering) on the surface chemical composition and work function of Indium Thin Oxide (ITO). While Ar+ sputtering removes carbon-based surface contaminants, it also modifies the Sn-rich surface of ITO and leads to a reduction of the oxidation state of Sn from Sn4+ to Sn2+. The decrease in the work function of ITO is directly correlated to the decrease of Sn atomic concentration in the Sn-rich top surface layer and the reduction of the oxidation state of surface Sn.

  17. Development of Compact Ozonizer with High Ozone Output by Pulsed Power

    Science.gov (United States)

    Tanaka, Fumiaki; Ueda, Satoru; Kouno, Kanako; Sakugawa, Takashi; Akiyama, Hidenori; Kinoshita, Youhei

    Conventional ozonizer with a high ozone output using silent or surface discharges needs a cooling system and a dielectric barrier, and therefore becomes a large machine. A compact ozonizer without the cooling system and the dielectric barrier has been developed by using a pulsed power generated discharge. The wire to plane electrodes made of metal have been used. However, the ozone output was low. Here, a compact and high repetition rate pulsed power generator is used as an electric source of a compact ozonizer. The ozone output of 6.1 g/h and the ozone yield of 86 g/kWh are achieved at 500 pulses per second, input average power of 280 W and an air flow rate of 20 L/min.

  18. Ozone kinetics in low-pressure discharges

    Science.gov (United States)

    Guerra, Vasco; Marinov, Daniil; Guaitella, Olivier; Rousseau, Antoine

    2012-10-01

    Ozone kinetics is quite well established at atmospheric pressure, due to the importance of ozone in atmospheric chemistry and to the development of industrial ozone reactors. However, as the pressure is decreased and the dominant three-body reactions lose importance, the main mechanisms involved in the creation and destruction of ozone are still surrounded by important uncertainties. In this work we develop a self-consistent model for a pulsed discharge and its afterglow operating in a Pyrex reactor with inner radius 1 cm, at pressures in the range 1-5 Torr and discharge currents of 40-120 mA. The model couples the electron Boltzmann equation with a system of equations for the time evolution of the heavy particles. The calculations are compared with time-dependent measurements of ozone and atomic oxygen. Parametric studies are performed in order to clarify the role of vibrationally excited ozone in the overall kinetics and to establish the conditions where ozone production on the surface may become important. It is shown that vibrationally excited ozone does play a significant role, by increasing the time constants of ozone formation. Moreover, an upper limit for the ozone formation at the wall in these conditions is set at 10(-4).

  19. Surface ozone and carbon monoxide levels observed at Oki, Japan: regional air pollution trends in East Asia.

    Science.gov (United States)

    Sikder, Helena Akhter; Suthawaree, Jeeranut; Kato, Shungo; Kajii, Yoshizumi

    2011-03-01

    Simultaneous ground-based measurements of ozone and carbon monoxide were performed at Oki, Japan, from January 2001 to September 2002 in order to investigate the O(3) and CO characteristics and their distributions. The observations revealed that O(3) and CO concentrations were maximum in springtime and minimum in the summer. The monthly averaged concentrations of O(3) and CO were 60 and 234 ppb in spring and 23 and 106 ppb in summer, respectively. Based on direction, 5-day isentropic backward trajectory analysis was carried out to determine the transport path of air masses, preceding their arrival at Oki. Comparison between classified results from present work and results from the year 1994-1996 was carried out. The O(3) and CO concentration results of classified air masses in our analysis show similar concentration trends to previous findings; highest in the WNW/W, lowest in N/NE and medium levels in NW. Moreover, O(3) levels are higher and CO levels are lower in the present study in all categories. Copyright © 2010 Elsevier Ltd. All rights reserved.

  20. Understanding Differences in Chemistry Climate Model Projections of Stratospheric Ozone

    Science.gov (United States)

    Douglass, A. R.; Strahan, S. E.; Oman, L. D.; Stolarski, R. S.

    2014-01-01

    Chemistry climate models (CCMs) are used to project future evolution of stratospheric ozone as concentrations of ozone-depleting substances (ODSs) decrease and greenhouse gases increase, cooling the stratosphere. CCM projections exhibit not only many common features but also a broad range of values for quantities such as year of ozone return to 1980 and global ozone level at the end of the 21st century. Multiple linear regression is applied to each of 14 CCMs to separate ozone response to ODS concentration change from that due to climate change. We show that the sensitivity of lower stratospheric ozone to chlorine change Delta Ozone/Delta inorganic chlorine is a near-linear function of partitioning of total inorganic chlorine into its reservoirs; both inorganic chlorine and its partitioning are largely controlled by lower stratospheric transport. CCMs with best performance on transport diagnostics agree with observations for chlorine reservoirs and produce similar ozone responses to chlorine change. After 2035, differences in Delta Ozone/Delta inorganic chlorine contribute little to the spread in CCM projections as the anthropogenic contribution to inorganic chlorine becomes unimportant. Differences among upper stratospheric ozone increases due to temperature decreases are explained by differences in ozone sensitivity to temperature change Delta Ozone/Delta T due to different contributions from various ozone loss processes, each with its own temperature dependence. Ozone decrease in the tropical lower stratosphere caused by a projected speedup in the Brewer-Dobson circulation may or may not be balanced by ozone increases in the middle- and high-latitude lower stratosphere and upper troposphere. This balance, or lack thereof, contributes most to the spread in late 21st century projections.

  1. Absorption of ozone by porous particles

    Energy Technology Data Exchange (ETDEWEB)

    Afanas' ev, V.P.; Dorofeev, S.B.; Sinitsyn, V.I.; Smirnov, B.M.

    1981-11-01

    The absorption of ozone by porous zeolite, silica gel, and activated carbon particles has been studied experimentally. It was shown that in addition to absorption, dissociation of ozone on the surface plays an important and sometimes decisive role. The results obtained were used to analyze the nature of ball lightning.

  2. Ozone: Good Up High, Bad Nearby

    Science.gov (United States)

    ... occurs in two layers of the atmosphere. The layer closest to the Earth’s surface is the troposphere. Here, ground- level or “ ... or use. Over time, these chemicals damage the earth’s protective ozone layer. What is Happening to the “Good” Ozone Layer? ...

  3. Summertime state-level source-receptor relationships between nitrogen oxides emissions and surface ozone concentrations over the continental United States.

    Science.gov (United States)

    Tong, Daniel Q; Mauzerall, Denise L

    2008-11-01

    Interstate transport of ozone (O3) and its precursors can contribute substantially to state-level surface o3 concentrations, making it difficult for some states to meet the National Ambient Air Quality Standards (NAAQS) for O3 by limiting only their own emissions. We analyze the effect of interstate transport on surface O3 in each continental U.S. state in July 1996 using the community multiscale air quality (CMAQ) model. By examining the difference between a baseline simulation and perturbation simulations in which each state's nitrogen oxides (NOx) emissions are removed, we establish for the first time a summertime source-receptor matrix for all 48 continental states. We find that for 16 (20) states at least one neighboring state's NOx emissions are responsible for a larger increase in monthly mean peak 8 h (all-hour) O3 concentrations than the state's own emissions. For over 80% of the contiguous states, interstate transport is more importantthan local emissions for summertime peak O3 concentrations. Our source-receptor matrices indicate that the geographic range of the clean air interstate rule (CAIR) was sufficient to address interstate transport of O3 in most of the states included in the program. However, the exclusion of Texas, which has particularly large NOx emissions, from the CAIR O3 program left emission sources uncontrolled that contribute more than 1 ppbv to the July mean of peak 8 h O3 concentrations in over a dozen states.

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

    Directory of Open Access Journals (Sweden)

    P. A. Newman

    2009-03-01

    Full Text Available Ozone depletion by chlorofluorocarbons (CFCs was first proposed by Molina and Rowland in their 1974 Nature paper. Since that time, the scientific connection between ozone losses and CFCs and other ozone depleting substances (ODSs has been firmly established with laboratory measurements, atmospheric observations, and modeling studies. This science research led to the implementation of international agreements that largely stopped the production of ODSs. In this study we use a fully-coupled radiation-chemical-dynamical model to simulate a future world where ODSs were never regulated and ODS production grew at an annual rate of 3%. In this "world avoided" simulation, 17% of the globally-averaged column ozone is destroyed by 2020, and 67% is destroyed by 2065 in comparison to 1980. Large ozone depletions in the polar region become year-round rather than just seasonal as is currently observed in the Antarctic ozone hole. Very large temperature decreases are observed in response to circulation changes and decreased shortwave radiation absorption by ozone. Ozone levels in the tropical lower stratosphere remain constant until about 2053 and then collapse to near zero by 2058 as a result of heterogeneous chemical processes (as currently observed in the Antarctic ozone hole. The tropical cooling that triggers the ozone collapse is caused by an increase of the tropical upwelling. In response to ozone changes, ultraviolet radiation increases, more than doubling the erythemal radiation in the northern summer midlatitudes by 2060.

  5. Multi-model assessment of stratospheric ozone return dates and ozone recovery in CCMVal-2 models