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  • 1
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1997
    In:  Geophysical Research Letters Vol. 24, No. 2 ( 1997-01-15), p. 171-172
    In: Geophysical Research Letters, American Geophysical Union (AGU), Vol. 24, No. 2 ( 1997-01-15), p. 171-172
    Type of Medium: Online Resource
    ISSN: 0094-8276
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1997
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  • 2
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1998
    In:  Journal of Geophysical Research: Atmospheres Vol. 103, No. D1 ( 1998-01-20), p. 1503-1511
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 103, No. D1 ( 1998-01-20), p. 1503-1511
    Abstract: The atmospheric burden of halons has continued to increase in recent years, despite an international ban on their production and sales in developed nations as of January 1, 1994. Halon emissions persist because of a lack of suitable substitutes for critical uses as fire extinguishants. As of January 1, 1997, halons H‐1301 (CBrF 3 ), H‐1211 (CBrClF 2 ), and H‐2402 (CBr 2 F 4 ) were present in the troposphere at 2.3±0.1, 3.5±0.1, and 0.45±0.03 pmol mol −1 . During 1995–1996 the tropospheric mole fraction of H‐1301 increased at 0.044±0.011 pmol mol −1 yr −1 , while that for H‐1211 grew at 0.16±0.016 pmol mol −1 yr −1 . These increases are significant and of concern because of the efficiency of bromine in depleting stratospheric ozone and because of the long atmospheric lifetimes of these gases. Given the current atmospheric record and the reported amount of halon produced before the ban on production, emission of H‐1301 at the 1995–1996 rate could continue for another 40 years, but H‐1211 would be depleted in 8–12 years. Exemptions to the ban on production may extend these periods. Tropospheric H‐2402 is increasing at 9±1 fmol mol −1 yr −1 , but historical data on its production and use are lacking.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1998
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    detail.hit.zdb_id: 3094268-8
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    SSG: 16,13
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  • 3
    In: Nature, Springer Science and Business Media LLC, Vol. 399, No. 6738 ( 1999-6), p. 749-755
    Type of Medium: Online Resource
    ISSN: 0028-0836 , 1476-4687
    RVK:
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    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1999
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  • 4
    Online Resource
    Online Resource
    American Association for the Advancement of Science (AAAS) ; 1995
    In:  Science Vol. 267, No. 5200 ( 1995-02-17), p. 1002-1005
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 267, No. 5200 ( 1995-02-17), p. 1002-1005
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
    RVK:
    RVK:
    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 1995
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  • 5
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1995
    In:  Journal of Geophysical Research: Atmospheres Vol. 100, No. D6 ( 1995-06-20), p. 11393-11401
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 100, No. D6 ( 1995-06-20), p. 11393-11401
    Abstract: Three oxygenated hydrocarbons were measured in ambient air above a rural forested site in western Alabama. Mixing ratios of methyl vinyl ketone (MVK), methacrolein (MACR), and 3‐methyl furan were determined during a 3‐week period in the summer of 1992. While the mean mixing ratio for methyl vinyl ketone was determined to be 740 parts per 10 12 (ppt), the mean mixing ratio for methacrolein was 480 ppt. The results for methyl vinyl ketone and methacrolein are compared to previously reported measurements from this same location during the summer of 1990. Although isoprene levels were lower by ∼50% in 1992, mixing ratios of the carbonyls were reduced by only ∼25%. These differences are discussed in light of the changes that had occurred to the forest canopy in the time elapsed between the two measurement campaigns. Despite the differences observed during the 2 years, a consistent diurnal variability is observed for methyl vinyl ketone, relative to methacrolein, during both years. In addition to a weak correlation observed between the carbonyls and temperature, levels of MVK and MACR in air sampled from just above the forest canopy are influenced by the depth of the mixed layer. A third oxidation product of isoprene, 3‐methyl furan, was identified and measured in ambient air. Mean daytime mixing ratios were estimated at 60 ppt. Nighttime levels were lower, averaging 40 ppt. Mixing ratios of 3‐methyl furan were highly correlated with isoprene (R 2 = 0.82), and during the day, were typically ∼2% of levels measured for isoprene.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1995
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  • 6
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1995
    In:  Journal of Geophysical Research: Atmospheres Vol. 100, No. D12 ( 1995-12-20), p. 25945-25963
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 100, No. D12 ( 1995-12-20), p. 25945-25963
    Abstract: An automated gas Chromatographic system was employed at a rural site in western central Alabama to measure atmospheric hydrocarbons and oxygenated hydrocarbons (oxy‐hydrocarbons) on an hourly basis from June 8 to July 19, 1990. The location, which was a designated site for the Southern Oxidant Study (SOS), was instrumented for a wide variety of measurements allowing the hydrocarbon and oxy‐hydrocarbon measurements to be interpreted both in terms of meteorological data and as part of a large suite of gas phase measurements. Although the site is situated in a Loblolly pine plantation, isoprene was observed to be the dominant hydrocarbon during the daytime with afternoon maxima of about 7 parts per billion by volume (ppbv). Decrease of isoprene after sunset was too rapid to be accounted for solely on the basis of gas phase chemistry. During the nighttime, α‐pinene and β‐pinene were the dominant hydrocarbons of natural origin. The ratio of α‐pinene to β‐pinene showed a well‐defined diurnal pattern, decreasing by more than 30% during the night; a decrease that could be understood on the basis of local gas phase chemistry. Oxy‐hydrocarbons, dominated by methanol and acetone, were the most abundant compounds observed. On a carbon atom basis, the oxy‐hydrocarbons contributed about 46% of the measured atmospheric burden during the daytime and about 40% at night. The similarity of the observed diurnal methanol variation to that of isoprene and subsequent measurements [ McDonald and Fall , 1993] indicate that much of the observed methanol was of local biogenic origin. Correlation of acetone with methanol suggests that it, also, has a significant biogenic source. In spite of the site's rural location, anthropogenic hydrocarbons constituted, on a carbon atom basis, about 21% of the hydrocarbon burden measured during the daytime and about 55% at night. Significant diurnal variations of the anthropogenic hydrocarbons, with increases at night, appeared to be driven by the frequent formation of a shallow nocturnal boundary layer.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1995
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    detail.hit.zdb_id: 710256-2
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  • 7
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1995
    In:  Journal of Geophysical Research: Atmospheres Vol. 100, No. D11 ( 1995-11-20), p. 22805-22813
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 100, No. D11 ( 1995-11-20), p. 22805-22813
    Abstract: Alkyl nitrates (RONO 2 ) and alkanes (RH) were measured at Scotia, Pennsylvania, in 1988 and at the Kinterbish Wildlife Area, Alabama, in 1992. A simple kinetic analysis was developed to relate the two species' concentrations based on the analytical solution of two sequential first‐order reactions using OH chemistry, RONO 2 photolysis, and assuming peroxy radicals (ROO) + NO as the source of RONO 2 . The analysis predicts an increase in RONO 2 /RH ratio with time. The C 4 and C 5 secondary alkyl nitrate/alkane ratios vary in a manner consistent with ROO + NO chemistry as their only source and photolysis and OH reaction as their only sinks. Comparison of ambient measurements of these compounds with predictions indicate that measured air masses experienced photochemical processing times consistent with alkyl nitrate evolution times between 0.1 and 5 days. The relationships of ethyl nitrate, n‐propyl nitrate and 2‐propyl nitrate ratios to their parent alkanes all indicate additional sources of RONO 2 , probably of a photochemical nature. Decomposition of larger alkoxy radicals are discussed as one possible source of smaller ROO radicals.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1995
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  • 8
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 272, No. 5266 ( 1996-05-31), p. 1318-1322
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
    RVK:
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 1996
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