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At least 289 records · Page 16

Evidence of the mid-latitude impact of Antarctic ozone depletion

Record low ozone values found over Australia and New Zealand during December 1987 following the record low Antarctic values of October 1987 are analyzed. The sudden decline of ozone amounts in midmonth rule out photochemical effects as a cause and permit the underlying processes to be investigated on a case study basis. Using data from ozone sondes, radiosondes, the Nimbus-7 total ozone mapping spectrometer, and meteorological analyses from the National Meteorological Center, it is argued that these low values resulted from transport of ozone-poor air from higher latitudes. Thus, it seems that the chemical destruction of ozone over Antarctica in early spring is having an impact on lower latitudes.

Atkinson, Roger J.↗

Quasi-biennial modulation of the Antarctic ozone depletion

The quasi-biennial oscillation (QBO) in total ozone and temperature has been extracted from 9 years of Total Ozone Mapping Spectrometer (TOMS) observations and National Meteorological Center (NMC) analyses. Years in which QBO-related variations in the total ozone and temperature are positive are found to correspond to years with smaller September Antarctic total ozone hole decline rates and vice versa. The QBO appears to be responsible for September decline rate deviations up to 0.4 Dobson units (DU) per day. Also, the QBO at mid-latitudes appears to be better correlated with the 30-mbar tropical QBO winds than with those at 50 mbar. Possible mechanisms that would explain these phenomena are discussed.

Lait, Leslie R.↗

Ozone depletion, greenhouse gases, and climate change

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.

Mooney, Harold A.↗

Spatial variation of ozone depletion rates in the springtime Antarctic polar vortex

An area-mapping technique, designed to filter out synoptic perturbations of the Antarctic polar vortex such as distortion or displacement away from the pole, was applied to the Nimbus-7 TOMS (Total Ozone Mapping Spectrometer) data. This procedure reveals the detailed morphology of the temporal evolution of column O3. The results for the austral spring of 1987 suggest the existence of a relatively stable collar region enclosing an interior that is undergoing large variations. A simplified photochemical model of O3 loss and the temporal evolution of the area-mapped polar O3 are used to constrain the chlorine monoxide (ClO) concentrations in the springtime Antarctic vortex. The O3 loss rates could be larger than deduced here because of underestimates of total O3 by TOMS near the terminator.

Yung, Yuk L.↗

Analysis of the eight-year trend in ozone depletion from empirical models of solar backscattered ultraviolet instrument degradation

Arguments are presented showing that the basic empirical model of the solar backscatter UV (SBUV) instrument degradation used by Cebula et al. (1988) in their analysis of the SBUV data is likely to lead to an incorrect estimate of the ozone trend. A correction factor is given as a function of time and altitude that brings the SBUV data into approximate agreement with the SAGE, SME, and Dobson network ozone trends. It is suggested that the currently archived SBUV ozone data should be used with caution for periods of analysis exceeding 1 yr, since it is likely that the yearly decreases contained in the archived data are too large.

Herman, J. R.↗

Anomalous molecular abundances and the depletion of NH2 in Comet P/Giacobini-Zinner

Observations of the CN, C2, C3, and NH2 molecules in spectra of the Comet P/Giacobini-Zinner (P/G-Z) obtained during the 1985 apparition are presented. Haser-model production rates are derived, and it is found that Q(C2)/Q(CN) and Q(C3)/Q(CN) are low compared to those in normal comets. This indicates that C2 and C3 were underabundance in P/G-Z, in agreement with previous results. Q(NH2)/Q(CN) is determined for five comets for the first time to determine a 'normal' value for this ratio. The ratio for P/G-Z is low compared to the value for the ensemble, suggesting that NH2 was underabundant. For the five-comet sample, Q(C3)/Q(CN) exhibits a strong dependence with heliocentric distance, in contrast to Q(C2)/Q(CN) and Q(C3)/Q(CN). The dust-to-gas ratio is characterized by calculating the product of the dust-grain albedo, the filling factor, and the projected radius of the aperture and by computing the dust-to-gas mass ratio.

Beaver, John E.↗

What Could Be Causing Global Ozone Depletion

The reported decline trend in global ozone between 1970 and 1986 may be in part an artifact of the analysis; the trend value appears to depend on the time interval selected for analysis--in relation to the 11-year solar cycle. If so, then the decline should diminish as one approaches solar maximum and includes data from 1987 to 1990. If the decline is real, its cause could be the result of natural and human factors other than just chlorofluorocarbons.

Singer, S. Fred↗

The potential for ozone depletion in the Arctic polar stratosphere

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 (CHl and ClONO2) was converted by reactions on polar stratospheric clouds to reactive ClO and Cl2O2 thoroughout the Arctic polar vortex before midwinter. Reactive nitrogen was converted to HNO3, and some, with spatial inhomogeneity, fell out of the stratosphere. These chemical changes ensured characteristic ozone losses of 10 to 15 percent at altitudes inside the polar vortex where polar stratospheric clouds had occurred. These local losses can translate into 5 to 8 percent losses in the vertical column abundance of ozone. As the amount of stratospheric chlorine inevitably increases by 50 percent over the next two decades, ozone losses recognizable as an ozone hole may well appear.

Brune, W. H.↗

More rapid polar ozone depletion through the reaction of HOCl with HCl on polar stratospheric clouds

The direct reaction of HOCl with HCl is shown here to play a critical part in polar ozone loss. Observations of high levels of OClO and ClO in the springtime Antarctic stratosphere confirm that most of the available chlorine is in the form of ClO(x). But current photochemical models have difficulty converting HCl to ClO(x) rapidly enough in early spring to account fully for the observations. Here, a chemical model is used to show that the direct reaction of HOCl with HCl provides the missing mechanism. As alternative sources of nitrogen-containing oxidants have been converted in the late autumn to inactive HNO3 by known reactions on the sulfate layer aerosols, the reaction of HOCl with HCl on polar stratospheric clouds becomes the most important pathway for releasing that stratospheric chlorine which goes into polar night as HCl.

Prather, Michael J.↗

A contribution toward understanding the biospherical significance of Antarctic ozone depletion

The paper presents and compares measurements of biologically active UV radiation made by the NSF scanning spectroradiometer (UV-monitor) at Palmer Station, Antarctica, during the Austral springs of 1988, 1989, and 1990. Column ozone abundance above Palmer Station is computed from these measurements using a multiple wavelength algorithm. Two contrasting action spectra are employed to estimate the biologically relevant dose from the spectral measurements: a standard weighting function for damage to DNA, and a new action spectrum representing the potential for photosynthesis inhibition in Antarctic phytoplankton. The former weights only UV-B wavelengths (280-320 nm) and gives the most weight to wavelengths shorter than 300 nm, while the latter includes large contributions out to 355 nm. Ozone abundances and dose-weighted irradiances provided by the NSF UV-monitor are used to derive the radiation amplification factors for both DNA- and phytoplankton-effective irradiance.

Lubin, Dan↗

Ozone depletion in the upper stratosphere estimated from satellite and Space Shuttle data

Shuttle Solar Backscatter Ultraviolet (SSBUV) spectrometer observations of ozone concentrations in the upper stratosphere made in October 1989 are combined here with measurements made in October 1980 by the similar SBUV instruments on NASA's Nimbus-7 satellite. It is shown that the ozone concentration near 45 km has decreased during this period by about 7 +/- 2 percent. The trend is consistent with predictions of a 2D photochemical model.

Hilsenrath, Ernest↗

CH4 production via CO2 reduction in a temperate bog - A source of (C-13)-depleted CH4

The paper reports measurements, taken over two annual cycles, of the flux and delta(C-13) of CH4 released from an acidic peat bog located in the foothills of the Cascade Range in Washington state, U.S. Measurements of the rate of aceticlastic methanogenesis and CO2 reduction in peat soil, using (C-14)-labeled acetate and sodium bicarbonate, show that acetate was not an important CH4 precursor and that CO2 reduction could account for all of the CH4 production. The in situ kinetic isotope effect for CO2 reduction, calculated using the delta-(C-13) of soil water CO2 and CH4 flux, was 0.932 +/- 0.007.

Lansdown, J. M.↗

Future chlorine-bromine loading and ozone depletion

The prediction of future ozone requires three elements: (1) a scenario for the net emissions of chemically and radiatively active trace gases from the land and oceans; (2) a global atmospheric model that projects the accumulation of these gases; and (3) a chemical transport model that describes the distribution of ozone for a prescribed atmospheric composition and climate. This chapter, of necessity, presents models for all three elements and focuses on the following: (1) atmospheric abundance of chlorine and bromine in the form of halocarbons; and (2) the associated perturbations to stratospheric ozone.

Prather, Michael J.↗

Interferometric observations of non-maser SiO emission from circumstellar envelopes of AGB stars - Acceleration regions and SiO depletion

High- and medium-resolution images of SiO J = 2-1(V = 0) from the circumstellar envelopes (CSEs) of three oxygen-rich stars, Chi Cyg, RX Boo, and IK Tau, were obtained. The SIO images were found to be roughly circular, implying that the CSEs are spherically symmetric on angular-size scales of about 3-9 arcsec. The observed angular half-maximum intensity source radius is nearly independent of the LSR velocity for all three CSEs. Chi Cyg and RX Boo are argued to be less than 450 pc distant, and have mass-loss rates larger than about 10 exp -6 solar mass/yr. In Chi Cyg and RX Boo, the line profiles at the peak of the brightness distribution are rounded, typical of optically-thick emission from a spherical envelope expanding with a constant velocity. In the IK Tau line profiles, an additional narrower central component is present, probably a result of emission from an inner circumstellar shell with a significantly smaller expansion velocity than the extended envelope.

Sahai, Raghvendra↗