Nitrous oxide in fresh water systems - An estimate for the yield of atmospheric N2O associated with disposal of human waste
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Kaplan, W. A.↗
Engineering topics
Wofsy, S. C.
Publications and source records attributed to Wofsy, S. C..
Auroral recombination of N and O - A possible source for emission in the gamma and delta bands of NO
Radiative recombination of N and O provides a significant source for auroral emission in the gamma and delta bands of NO with selective population of vibrational levels in the A 2 Sigma(+) and C 2 Pi states. This mechanism may account for emissions detected near 2150 A. Models are derived for the auroral ionosphere and include estimates for the concentrations of N and NO. The concentration of NO is estimated to have a value of about 100 million per cu cm near 140 km in an IBC III aurora. The corresponding density for N is about 50 million per cu cm, and the concentration ratio NO(+)/O2(+) has a value of about 5.5.
Wofsy, S. C.↗
Nitrous oxide in fresh water systems: An estimate for the yield of atmospheric N2O associated with disposal of human waste
The N2O content of waters in the Potomac and Merrimack Rivers was measured on a number of occasions over the period April to July 1977. The concentrations of dissolved N2O exceeded those which would apply in equilibrium with air by factors ranging from about 46 in the Potomac to 1.2 in the Merrimack. Highest concentrations of dissolved N2O were associated with sewage discharges from the vicinity of Washington, D. C., and analysis indicates a relatively high yield, 1.3 to 11%, for prompt conversion of waste nitrogen to N2O. Measurements of dissolved N2O in fresh water ponds near Boston demonstrated that aquatic systems provide both strong sources and sinks for atmospheric N2O.
Kaplan, W. A.↗
Sources and sinks for atmospheric H2 - A current analysis with projections for the influence of anthropogenic activity
Oxidation of CH4 provides the major source for atmospheric H2, which is removed mainly by reaction with OH. Biological activity at earth's surface appears to represent at most a minor sink for H2. Anthropogenic activity is a significant source for both H2 and CO in the present atmosphere and may be expected to exert a growing influence in the future. Models are presented which suggest a rise in the mixing ratio of H2 from its present value of 5.6 ten-millionths to about 1.8 millionths by the year 2100. The mixing ratio of CO should grow from 9.7 hundred-millionths to 2.3 ten-millionths over the same time period, and there should be a rise in CH4 by about a factor of 1.5 associated with anthropogenically induced reductions in tropospheric OH.
Penner, J. E.↗
Sources and sinks for atmospheric N2O
Observations of the temporal and spatial distribution of N2O in solution are not yet sufficient to permit quantitative assessment of the role of the ocean in the budget of atmospheric N2O. Consideration of the global nitrogen cycle suggests that the land should be the primary source of N2O. The gas is removed in the atmosphere by photolysis and by reaction with O(1D), and there may be additional sinks in the ocean.
Mcelroy, M. B.↗
Interactions of CH4 and CO in the earth's atmosphere
Global distributions, sources, and sinks of methane and carbon monoxide in upper and lower levels of the earth's atmosphere, and the global budgets of methane and carbon monoxide, are studied, with emphasis on cumulative pollution. Stratospheric contents, vertical profiles of concentrations, simulation of vertical transport through the atmosphere, and latitudinal distributions are examined. Diffuse and localized (urban) concentrations of CO as pollutant are studied, and anthropogenic sources and sinks for CH4 and CO are considered. Perturbation of the CH4-CO-CO2 cycle, crucial to self-cleansing mechanisms of the troposphere, by anthropogenic CO emissions, and the effect of CO long life as global pollutant, are investigated.
Wofsy, S. C.↗
Atmospheric halocarbons - A discussion with emphasis on chloroform
Bleaching of paper pulp represents a major industrial use of chlorine and could provide an environmentally significant source of atmospheric halocarbons. The related global production of chloroform is estimated at 300,000 ton per year and there could be additional production associated with atmospheric decomposition of perchloroethylene. Estimates are given for the production of methyl chloride, methyl bromide and methyl iodide, 5.2 million, 77 thousand, and 740 thousand ton per year respectively. The relative yields of CH3Cl, CH3Br and CH3I are consistent with the hypothesis of a marine biological source for these compounds. Concentrations of other halocarbons observed in the atmosphere appear to indicate industrial sources.
Yung, Y. L.↗
The chemistry of atmospheric bromine
Bromine may act as a catalyst for recombination of ozone and could be more efficient than either nitric oxide or chlorine. The lower atmosphere contains small concentrations of gaseous bromine produced in part by marine activity and volatilization of particulate material released during the combustion of leaded gasoline, with an additional contribution due to the use of methyl bromide as an agricultural fumigant. Observations by Lazrus et al., (1975) indicate small concentrations of bromine, about 10 to the -11th power (v/v), in the contemporary stratosphere and appear to imply a reduction of approximately 0.3% in the global budget of O3. Estimates are given for future reductions in O3 which might occur if the use of CH3Br as an agricultural fumigant were to continue to grow at present rates.
Wofsy, S. C.↗
Freon consumption - Implications for atmospheric ozone
Freons are a potential source of stratospheric chlorine and may indirectly cause serious reductions in the concentration of ozone. The reduction could be as large as 3 percent by 1980, or 16 percent by 2000, if Freon consumption were to grow at 10 percent per year. Even if Freon use were terminated as early as 1990, it could leave a significant effect which might endure for several hundred years.
Wofsy, S. C.↗
Venus cloud models
Remote observations of Venus are reviewed. The strongest inferences of cloud properties can be drawn from polarization data which provide information about cloud particles near 68 km. Particle properties are not as well determined at higher and lower levels. If the clouds are generated photochemically from reduced sulfur species, the supply of O2 may be an important constraint on cloud production. Vapor-pressure data reviewed, and it is shown that deep clouds cannot be H2SO4-H2O aerosols unless the mixing ratios of both H2SO4 and H2O approach 0.001 below 50 km.
Wofsy, S. C.↗