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Ozone volcanic eruption effects

Through the natural processes of the UV rays of the sun passing through this layer, the absorbs the rays and is broken down to molecules and O atoms. This process is reversible, and ozone (O ) is constantly being reformed from UV effects on However, the separation can be accelerated faster than the reformation of new by induction of other chemical gases into the ozone layer. Of particular concern is that chlorine from CFCs and from other sources, such as the ocean and volcanic eruptions, combines with atomic oxygen that is broken down from Oj by UV radiation. It then forms chlorine monoxide (CIO), which means the atomic oxygen is not available for reformation into O by UV radiation. Herein lie the potential problem and the controversy. [Pg.231]

In short, the heterogeneous chemistry that drives the Antarctic ozone hole can occur not only on solid surfaces but also in and on liquid solutions containing combinations of HN03, H2S04, and HzO. As discussed in the following section, it is believed that this is why volcanic eruptions have such marked effects on stratospheric ozone on a global basis. [Pg.690]

The finding that the heterogeneous chemistry that occurs on polar stratospheric clouds also occurs in and on liquid solutions in the form of liquid aerosol particles and droplets in the atmosphere provided a key link in understanding the effects of volcanic eruptions on stratospheric ozone in both the polar regions and midlatitudes. As discussed herein, the liquid particles formed from volcanic emissions are typically 60-80 wt% H2S04-H20, and hence the chemistry discussed in the previous section can also occur in these particles (Hofmann and Solomon, 1989). We discuss briefly in this section the contribution of volcanic emissions to the chemistry of the stratosphere and to ozone depletion on a global scale. For a brief review of this area, see McCormick et al. (1995). [Pg.690]

Thus, the effect of heterogeneous bromine chemistry is primarily to amplify the chlorine-catalyzed destruction of ozone through the more rapid conversion of the reservoir species HC1 back into active forms of chlorine (Lary et al., 1996 Tie and Brasseur, 1996). This becomes particularly important under conditions of enhanced aerosol particles, e.g., after major volcanic eruptions. [Pg.706]

Second, reaction 8.9 and other relevant reactions appear to occur preferentially on available solid surfaces, which are often ice crystals but may also be particles of sulfate hazes from volcanic eruptions or human activity. Third, volatile bromine compounds are even more effective (via Br atoms) than chlorine sources at destroying ozone methyl bromide is released into the atmosphere naturally by forest fires and the oceans, but anthropogenic sources include the use of organic bromides as soil fumigants (methyl bromide, ethylene dibromide) and bromofluorocarbons as fire extinguishers (halons such as CFsBr, CF2BrCl, and C2F4Br2). [Pg.163]

Stenchikov G., Robock A., Ramaswamy V., Schwarzkopf M. D., Hamilton K., and Ramachandran S. (2002) Arctic Oscillation response to the 1991 Mount Knambo eruption effects of volcanic aerosols and ozone depletion. J. Geophys. Res. Doi 10.1029/2002JD002090 (28 December 2002). [Pg.1429]

The analysis of perturbations to the middle atmosphere must also include natural processes, such as the effects of volcanic eruptions, which produce large quantities of fine particles as well as water vapor and SO2, which eventually produces H2SO4 and sulfate aerosols. The amount of gas injected, the composition and the maximum altitude of injection vary with the intensity of the eruption. Such events can alter the budgets of some atmospheric constituents and are clearly reflected in the middle atmospheric aerosol content. Particles also provide sites for surface reactions to occur. Such heterogeneous reactions may activate chlorine and enhance the depletion of ozone by industrially manufactured halocarbons. [Pg.9]

The observed trends in the NAM towards higher indices may have resulted from human-induced changes in the temperature structure of the lower stratosphere in response to greenhouse gas emissions and ozone depletion (Shindell et al., 2001). The radiative effects of solar activity and of volcanic eruptions may also have produced NAM- like signatures detectable at the Earth s surface. The response of the Earth system to climate forcing may therefore involve changes in particular dynamical modes, and hence the human influence on climate at the Earth surface may occur in part by way of the stratosphere. [Pg.125]

It should be noted that the reaction sequences which convert S02 to sulfate do not modify the HOx budget (McKeen et al., 1984). The intrusion of large amounts of S02 in the stratosphere during volcanic eruptions could enhance the short-term amount of ozone in the middle atmosphere by direct chemical effects (Crutzen and Schmailzl, 1983 Bekki et al., 1993) through the following mechanism ... [Pg.391]

Volcanic injection of large quantities of sulfate aerosol into the stratosphere offers the opportunity to examine the sensitivity of ozone depletion and species concentrations to a major perturbation in aerosol surface area (Hofmann and Solomon 1989 Johnston et al. 1992 Prather 1992 Mills et al. 1993). The increase in stratospheric aerosol surface area resulting from a major volcanic eruption can lead to profound effects on C10 -induced ozone depletion chemistry. Because the heterogeneous reaction of N205 and water on the surface of stratospheric aerosols effectively removes N02 from the active reaction system, less N02 is available to react with CIO to form the reservoir species C10N02. As a result, more CIO is present in active CIO cycles. Therefore an increase in stratospheric aerosol surface area, as from a volcanic eruption, can serve to make the chlorine present more effective at ozone depletion, even if no increases in chlorine are occurring. [Pg.186]

The tremendous force of a volcanic eruption carries a sizable amount of gas into the stratosphere. There SO2 is oxidized to SO3, which is eventually converted to sulfuric acid aerosols in a series of complex reactions. In addition to destroying ozone in the stratosphere (see page 837), these aerosols can also affect climate. Because the stratosphere is above the atmospheric weather patterns, the aerosol clouds often persist for more than a year. They absorb solar radiation and thereby cause a drop in temperature at Earth s surface. However, this cooling effect is local rather than global, because it depends on the site and frequency of volcanic eruptions. [Pg.838]

Figure 6.23. The top panel shows the total tropospheric chlorine content estimated from the baseline scenario in WMO/UNEP (1998) this is based on a gas-by-gas analysis like those shown in Figure 6.22. The bottom panel shows the changes in the 5-year running mean ozone observed over Switzerland (Staehelin et al., 1998a,b) compared to a model calculation for 45°N applying the same time averaging, with and without considering the effects of volcanic enhancements in aerosol chemistry (from the model of Solomon et al., 1996 1998). The major eruptions since 1980 were those of El Chichon in 1982 and Mt. Pinatubo in 1991. Updated from Solomon (1999). Figure 6.23. The top panel shows the total tropospheric chlorine content estimated from the baseline scenario in WMO/UNEP (1998) this is based on a gas-by-gas analysis like those shown in Figure 6.22. The bottom panel shows the changes in the 5-year running mean ozone observed over Switzerland (Staehelin et al., 1998a,b) compared to a model calculation for 45°N applying the same time averaging, with and without considering the effects of volcanic enhancements in aerosol chemistry (from the model of Solomon et al., 1996 1998). The major eruptions since 1980 were those of El Chichon in 1982 and Mt. Pinatubo in 1991. Updated from Solomon (1999).

See other pages where Ozone volcanic eruption effects is mentioned: [Pg.56]    [Pg.694]    [Pg.695]    [Pg.719]    [Pg.359]    [Pg.496]    [Pg.710]    [Pg.57]    [Pg.187]    [Pg.29]    [Pg.210]    [Pg.64]    [Pg.108]    [Pg.842]    [Pg.517]    [Pg.906]    [Pg.76]    [Pg.145]    [Pg.694]    [Pg.696]    [Pg.497]    [Pg.498]    [Pg.684]   
See also in sourсe #XX -- [ Pg.155 ]




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