1993
DOI: 10.1126/science.259.5092.194
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Atmospheric Lifetimes of Long-Lived Halogenated Species

Abstract: These repair systems distinguish template DNA from newly synthesized DNA by the new DNA's unmethylated state. Thus, these systems can resolve DNA mismatches in favor of the unmutated allele. Other mismatch repair systems are not methyldirected and are presumabiy error prone (45).

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Cited by 532 publications
(419 citation statements)
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References 22 publications
(8 reference statements)
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“…The transport of H2-rich mesospheric air into the stratosphere is likely to occur in winter at high latitudes during the diabatic This has an important implication for mean age determinations since SF6 is decomposed by UV absorption ()• < 125 nm) and electron reactions [Ravishankara et al, 1993;Morris et al, 1995] that become relevant only in the mesosphere. If a significant amount of SF6-depleted air were transported downward into the stratosphere, the mean age determined in stratospheric air samples could be significantly biased towards higher SF6-age values.…”
Section: Mean Age Calculationmentioning
confidence: 99%
“…The transport of H2-rich mesospheric air into the stratosphere is likely to occur in winter at high latitudes during the diabatic This has an important implication for mean age determinations since SF6 is decomposed by UV absorption ()• < 125 nm) and electron reactions [Ravishankara et al, 1993;Morris et al, 1995] that become relevant only in the mesosphere. If a significant amount of SF6-depleted air were transported downward into the stratosphere, the mean age determined in stratospheric air samples could be significantly biased towards higher SF6-age values.…”
Section: Mean Age Calculationmentioning
confidence: 99%
“…SF 6 is released to the atmosphere predominantly in the middle latitudes of the Northern Hemisphere and is subsequently incorporated into the hydrosphere. The SF 6 atmospheric mixing ratio has rapidly increased because of (1) the long lifetime in the atmosphere, with estimates of 1935 [Patra et al, 1997] to 3200 [Ravishankara et al, 1993] years, (2) the low solubility of the tracer in water [Ashton et al, 1968; Cosgrove and Walkey, 1981; Mroczek, 1997], (3) the apparent high stability in soils [Maiss and Brenninkmeijer, 1998], and (4) the lack of other significant natural sinks [Maiss and Brenninkmeijet, 1998]. The SF 6 atmospheric mixing ratio increased from 0.6 parts per trillion volume (pptv) in 1976 [Maiss and Brenninkmeijer, 1998] to more than 4 pptv in 1999.…”
Section: Introductionmentioning
confidence: 99%
“…The GWP of these two molecules is very high, SF 6 being slightly higher because its atmospheric lifetime, ca. 3200 a [8], is about four times greater than that of SF 5 CF 3 . However, the contribution of these two molecules to the overall greenhouse effect is still very small because their atmospheric concentrations, despite rising rapidly at the rate of ca.…”
Section: The Physical Chemistry Properties Of Greenhouse Gasesmentioning
confidence: 94%
“…The averaging process thus needs input from a 2− or 3−dimensional model of the atmosphere in order to supply values for n i . This is essentially a meterological, and not a chemical Many such studies have been made for SF 6 [8,12,13], and differences in the kinetic model (k i ) and the atmospheric distributions (n i ) from different climate or transport models account for the variety of atmospheric lifetimes that have been reported. The importance of both these factors has also been explored by Hall and Waugh [14].…”
Section: The Lifetime Of a Greenhouse Gas In The Earth's Atmospherementioning
confidence: 99%
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