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Variations in the isotopic composition of carbon in urban atmospheric carbon dioxide.

Measurement of the abundance of atmospheric carbon dioxide as an indicator of air pollution has been of very limited value because of variations in urban areas in the substantial concentration of natural carbon dioxide produced from combustion and noncombustion (natural) sources. A solution to this problem is the use of precise isotopic assay of ratios of carbon-13 to carbon-12 in atmospheric carbon dioxide. There is very little variation of carbon isotopic composition in samples taken over rural or urban areas where rapid mixing and diffusion of gaseous combustion products is possible. Significant differences in this composition in samples taken at centrally located points at street level in the lower Manhattan business district show an increase in concentration of atmospheric carbon dioxide of roughly 20 percent produced primarily by automobile exhaust.

Air Pollution↗

Carbon monoxide: residence time in the atmosphere.

A lower limit of 0.1 year for the residence time of carbon monIoxide in the atmosphere is derived from radiocarbon measurements. The action of certain microorganisms and atmospheric photochemical reactions are possible mechanisms for the removal of carbon monoxide. This value can be compared with 2.7 years, a value deduced from estimated rates of carbon monoxide production and global measurements of atmospheric concentrations of carbon monoxide.

Air Pollution↗

Radio Frequency Signals in Jupiter's Atmosphere

During the Galileo probe's descent through Jupiter's atmosphere, under the ionosphere, the lightning and radio emission detector measured radio frequency signals at levels significantly above the probe's electromagnetic noise. The signal strengths at 3 and 15 kilohertz were relatively large at the beginning of the descent, decreased with depth to a pressure level of about 5 bars, and then increased slowly until the end of the mission. The 15-kilohertz signals show arrival direction anisotropies. Measurements of radio frequency wave forms show that the probe passed through an atmospheric region that did not support lightning within at least 100 kilometers and more likely a few thousand kilometers of the descent trajectory. The apparent opacity of the jovian atmosphere increases sharply at pressures greater than about 4 bars.

Journal Article↗

The 18O/16O and 17O/16O ratios in atmospheric nitrous oxide: A mass-independent anomaly

Measurements of the oxygen isotope ratios (18O/16O and 17O/16O) in atmospheric nitrous oxide (N2O) from La Jolla, Pasadena, and the White Mountain Research Station (elevation, 3801 meters) in California and the White Sands Missile Range in New Mexico show that N2O has a mass-independent composition. These data suggest the presence of a previously undefined atmospheric process. The La Jolla samples can be explained by a mixing between an atmospherically derived source of mass-independent N2O and biologically derived mass-dependent N2O. Possible origins of the mass-independent anomaly in N2O are discussed.

Journal Article↗

Time scales in atmospheric chemistry: coupled perturbations to N2O, NOy, and O3

Nitrous oxide (N2O) is one of the top three greenhouse gases whose emissions may be brought under control through the Framework Convention on Climate Change. Current understanding of its global budget, including the balance of natural and anthropogenic sources, is largely based on the atmospheric losses calculated with chemical models. A representative one-dimensional model used here describes the photochemical coupling between N2O and stratospheric ozone (O3), which can easily be decomposed into its natural modes. The primary, longest lived mode describes most of the atmospheric perturbation due to anthropogenic N2O sources, and this pattern may be observable. The photolytic link between O3 and N2O is identified as the mechanism causing this mode to decay 10 to 15 percent more rapidly than the N2O mean atmospheric lifetime, affecting the inference of anthropogenic sources.

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Mass-independent oxygen isotope fractionation in atmospheric CO as a result of the reaction CO + OH

Atmospheric carbon monoxide (CO) exhibits mass-independent fractionation in the oxygen isotopes. An 17O excess up to 7.5 per mil was observed in summer at high northern latitudes. The major source of this puzzling fractionation in this important trace gas is its dominant atmospheric removal reaction, CO + OH --> CO2 + H, in which the surviving CO gains excess 17O. The occurrence of mass-independent fractionation in the reaction of CO with OH raises fundamental questions about kinetic processes. At the same time the effect is a useful marker for the degree to which CO in the atmosphere has been reacting with OH.

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A large terrestrial carbon sink in north america implied by atmospheric and oceanic carbon dioxide data and models

Atmospheric carbon dioxide increased at a rate of 2.8 petagrams of carbon per year (Pg C year-1) during 1988 to 1992 (1 Pg = 10(15) grams). Given estimates of fossil carbon dioxide emissions, and net oceanic uptake, this implies a global terrestrial uptake of 1.0 to 2. 2 Pg C year-1. The spatial distribution of the terrestrial carbon dioxide uptake is estimated by means of the observed spatial patterns of the greatly increased atmospheric carbon dioxide data set available from 1988 onward, together with two atmospheric transport models, two estimates of the sea-air flux, and an estimate of the spatial distribution of fossil carbon dioxide emissions. North America is the best constrained continent, with a mean uptake of 1.7 +/- 0.5 Pg C year-1, mostly south of 51 degrees north. Eurasia-North Africa is relatively weakly constrained, with a mean uptake of 0.1 +/- 0.6 Pg C year-1. The rest of the world's land surface is poorly constrained, with a mean source of 0.2 +/- 0.9 Pg C year-1.

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Global warming and marine carbon cycle feedbacks on future atmospheric CO2

A low-order physical-biogeochemical climate model was used to project atmospheric carbon dioxide and global warming for scenarios developed by the Intergovernmental Panel on Climate Change. The North Atlantic thermohaline circulation weakens in all global warming simulations and collapses at high levels of carbon dioxide. Projected changes in the marine carbon cycle have a modest impact on atmospheric carbon dioxide. Compared with the control, atmospheric carbon dioxide increased by 4 percent at year 2100 and 20 percent at year 2500. The reduction in ocean carbon uptake can be mainly explained by sea surface warming. The projected changes of the marine biological cycle compensate the reduction in downward mixing of anthropogenic carbon, except when the North Atlantic thermohaline circulation collapses.

Journal Article↗

Isotope fractionation and atmospheric oxygen: implications for phanerozoic O(2) evolution

Models describing the evolution of the partial pressure of atmospheric oxygen over Phanerozoic time are constrained by the mass balances required between the inputs and outputs of carbon and sulfur to the oceans. This constraint has limited the applicability of proposed negative feedback mechanisms for maintaining levels of atmospheric O(2) at biologically permissable levels. Here we describe a modeling approach that incorporates O(2)-dependent carbon and sulfur isotope fractionation using data obtained from laboratory experiments on carbon-13 discrimination by vascular land plants and marine plankton. The model allows us to calculate a Phanerozoic O(2) history that agrees with independent models and with biological and physical constraints and supports the hypothesis of a high atmospheric O(2) content during the Carboniferous (300 million years ago), a time when insect gigantism was widespread.

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A potent greenhouse gas identified in the atmosphere: SF(5)CF(3)

We detected a compound previously unreported in the atmosphere, trifluoromethyl sulfur pentafluoride (SF(5)CF(3)). Measurements of its infrared absorption cross section show SF(5)CF(3) to have a radiative forcing of 0.57 watt per square meter per parts per billion. This is the largest radiative forcing, on a per molecule basis, of any gas found in the atmosphere to date. Antarctic firn measurements show it to have grown from near zero in the late 1960s to about 0.12 part per trillion in 1999. It is presently growing by about 0.008 part per trillion per year, or 6% per year. Stratospheric profiles of SF(5)CF(3) suggest that it is long-lived in the atmosphere (on the order of 1000 years).

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Atmospheric CO2 concentrations over the last glacial termination.

A record of atmospheric carbon dioxide (CO2) concentration during the transition from the Last Glacial Maximum to the Holocene, obtained from the Dome Concordia, Antarctica, ice core, reveals that an increase of 76 parts per million by volume occurred over a period of 6000 years in four clearly distinguishable intervals. The close correlation between CO2 concentration and Antarctic temperature indicates that the Southern Ocean played an important role in causing the CO2 increase. However, the similarity of changes in CO2 concentration and variations of atmospheric methane concentration suggests that processes in the tropics and in the Northern Hemisphere, where the main sources for methane are located, also had substantial effects on atmospheric CO2 concentrations.

Journal Article↗

Growth of a bacterium under a high-pressure oxy-helium atmosphere.

Growth of a barotolerant marine organism, EP-4, in a glutamate medium equilibrated with an oxy-helium atmosphere at 500 atmospheres (atm; total pressure) (20 degrees C) was compared with control cultures incubated at hydrostatic pressures of 1 and 500 atm. Relative to the 1-atm control culture, incubation of EP-4 at 500 atm in the absence of an atmosphere resulted in an approximately fivefold reduction in the growth rate and a significant but time variant reduction in the rate constants for the incorporation of substrate into cell material and respiration. Distinct from the pressurized control and separate from potential effects of dissolution of helium upon decompression of subsamples, exposure of the organism to high-pressure oxy-helium resulted in either a loss of viability of a large fraction of the cells or the arrest of growth for one-third of the experimental period. After these initial effects, however, the culture grew exponentially at a rate which was three times greater than the 500-atm control culture. The rate constant for the incorporation of substrate into cell material was also enhanced twofold in the presence of high-pressure oxy-helium. Dissolved oxygen was well controlled in all of the cultures, minimizing any potential toxic effects of this gas.

Journal Article↗

Airborne Bacteria in the Atmospheric Surface Layer: Temporal Distribution above a Grass Seed Field.

Temporal airborne bacterial concentrations and meteorological conditions were measured above a grass seed field in the Willamette River Valley, near Corvallis, Oreg., in the summer of 1993. The concentration of airborne bacteria had a maximum of 1,368.5 CFU/m(sup3), with a coefficient of variation of 90.5% and a mean of 121.3 CFU/m(sup3). The lowest concentration of bacteria occurred during the predawn hours, with an average of 32.2 CFU/m(sup3), while sunrise and early evening hours had the highest averages (164.7 and 158.1 CFU/m(sup3), respectively). The concentrations of bacteria in the atmosphere varied greatly, with a maximum difference between two 2-min samples of 1,995 CFU/m(sup3). The concentrations of bacteria in the atmosphere could be divided into five time periods during the day that were thought to be related to the local diurnal sea breeze and Pacific Coast monsoon weather conditions as follows: (i) the nighttime minimum concentration, i.e., 2300 to 0600 h; (ii) the sunrise peak concentration, i.e., 0600 to 0800 h; (iii) the midday accumulating concentration, i.e., 0800 to 1515 h; (iv) the late-afternoon sea breeze trough concentration, i.e., 1515 to 1700 h; and (v) the evening decrease to the nighttime minimum concentration, i.e., 1700 to 2300 h. The sunrise peak concentration (period ii) is thought to be a relatively general phenomenon dependent on ground heating by the sun, while the afternoon trough concentration is thought to be a relatively local phenomenon dependent on the afternoon sea breeze. Meteorological conditions are thought to be an important regulating influence on airborne bacterial concentrations in the outdoor atmosphere in the Willamette River Valley.

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Atmospheric Methane Consumption by Forest Soils and Extracted Bacteria at Different pH Values.

The effect of pH on atmospheric methane (CH4) consumption was studied with slurries of forest soils and with bacteria extracted from the same soils. Soil samples were collected from a mixed hardwood stand in New Hampshire, from jackpine and aspen stands at the BOREAS (Boreal Ecosystem Atmosphere Study) site near Thompson, northern Manitoba, from sites in southern Québec, including a beech stand and a meadow, and from a site in Ontario (cultivated humisol). Consumption of atmospheric CH4 (concentration, approximately 1.8 ppm) occurred at depths of >5 cm in both acidic (pH 4.5 to 5.2) and alkaline (pH 7.2 to 7.8) soils. In slurries of acidic soils, maximum activity occurred at different pH values (pH 4.0 to 6.5). Bacteria extracted from these soils by high-speed blending and density gradient centrifugation showed pH responses different from the pH responses of the slurries. In all cases, these bacteria had a methanotrophy pH optimum of 5.8 and exhibited no activity at pH 6.8 to 7.0, the pH optimum range for known methanotrophs. This difference in pH responses could be useful in modifying media currently used for isolation of these organisms. Methanotrophic activity was induced in previously non-CH4-consuming soils by preincubation with 5% (vol/vol) CH4 (50,000 µl of CH4 per liter) or by liquid enrichment with 20% CH4. The bacteria showed pH responses typical of known methanotrophs and not typical of preexisting consumers of ambient CH4. Furthermore, methanotrophs induced by high CH4 levels were more readily extracted from soil than preexisting ambient CH4 consumers were. In the alkaline soils, preexisting activity either was destroyed or resisted extraction by the procedure used. The results support the hypothesis that consumers of ambient CH4 in soils are physiologically distinct from the known methanotrophs.

Journal Article↗

Effects in hyperoxia upon microorganisms. I. Membrane culture technique for exposing cells directly to test atmospheres.

A membrane culture technique was developed for directly exposing microorganisms to test atmospheres. Inhibition and killing were calculated from comparisons with air-grown cultures. Direct colony counts were used with low inocula. With mass inocula, plate colony counts and optical-density measurements were made on resuspended filter populations. Bacteria, including Escherichia coli, were more sensitive to oxygen than previously reported. With inocula of a few hundred cells per membrane, five of seven species failed to produce colonies while exposed to oxygen at one atmosphere. Upon reincubation in air, the survival of five species ranged from near 0 to 12% of the cells. Aerobacter aerogenes was neither inhibited nor killed. With this technique, bacteria are in direct contact with the test atmosphere and cells which survive are detected but do not obscure the response of other cells in the population.

Bacillus cereus↗

Survival of Aspergillus flavus and Fusarium moniliforme in high-moisture corn stored under modified atmospheres.

Freshly harvested high-moisture corn with 29.4% moisture and corn remoistened to 19.6% moisture were inoculated with Aspergillus flavus Link ex Fr. and stored for 4 weeks at about 27 C in air (0.03% CO2, 21% O2, and 78% N2) and three modified atmospheres: (i) 99.7% N2 and 0.3% O2; (ii) 61.7% CO2, 8.7% O2, and 29.6% N2; and (iii) 13.5% CO2, 0.5% O2, and 84.8% N2. Kernel infections by A. flavus, Fusarium moniliforme (Sheld.) Snyd. et Hans., and other fungi were monitored weekly. The modified-atmosphere treatments delayed deterioration by A. flavus and F. moniliforme, but their growth was not completely stopped. A. flavus survived better in the remoistened than in the freshly harvested corn. F. moniliforme survived in both. A. flavus and F. moniliforme were the dominant fungi in corn removed from the modified atmospheres and exposed to normal air for 1 week.

Air↗

Respiratory illness in British schoolchildren and atmospheric smoke and sulphur dioxide 1973-7. I: cross-sectional findings.

The relation between respiratory illness and atmospheric smoke and sulphur dioxide (SO2) was investigated from 1973 to 1977 in children aged 6 to 11 from a random sample of 28 areas in England and Scotland. Cross-sectional results are presented for 1975, and results from other years briefly summarised. In 1975 there were 19 areas with data on pollution and in these areas the sample included 5787 children of white ethnic origin of whom 4116 (71%) had complete information of respiratory illness and other variables considered in the analysis. After allowing for the effects of age, social class, population density, type of fuel used for cooking in the home, and season of examination, the prevalence of respiratory illness in both sexes was in the home, and season of examination, the prevalence of respiratory illness in both sexes was positively associated with the levels of smoke over the range of annual means 8 to 51 microgram/m3 )P less than or equal to 0.05). No relation was found between illness and annual means of SO2 ranging from 12 to 114 microgram/m3. Similar results were found in other years, and in 1977, when information of tobacco smoking at home was collected, the association between illness and atmospheric smoke appeared to be independent of smoking within the home. The levels of smoke were much lower than those at which effects on health hve previously been reported so the association is unlikely to be causative. We postulate that higher levels of atmospheric pollution at an earlier period in some areas may have predisposed children living there to respiratory illness during their primary school years. Alternatively, some other characteristics of the polluted areas may explain the findings.

Air Pollution↗

Effect of incubation atmosphere and temperature on isolation of Campylobacter jejuni from human stools.

To determine the optimal conditions for isolation of Campylobacter jejuni from human fecal specimens, we compared incubation atmospheres that contained about 5, 10, and 15% oxygen with the 17% oxygen produced in candle jars and also compared incubation temperatures of 37 and 42 degrees C. At 42 degrees C, C. jejuni was isolated from all 16 specimens; however, colony sizes were larger when plates were incubated in 5 and 10% oxygen than in the other two atmospheres. At 37 degrees C some positive cultures were missed in 15% oxygen and in the candle jar. The largest colony sizes were obtained in 5% oxygen. For each atmospheric condition tested, the colonies were larger at 42 than at 37 degrees C. When incubation is done at 42 degrees C, use of a candle jar is adequate; however, at 37 degrees C candle jars should not be used for isolation of C. jejuni from human feces.

Campylobacter↗