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  • AGU (American Geophysical Union)  (3)
  • 2005-2009  (3)
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  • 1
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    AGU (American Geophysical Union)
    In:  Journal of Geophysical Research: Atmospheres, 112 . D09312.
    Publication Date: 2018-02-06
    Description: Natural sources of bromoform (CHBr3) and dibromomethane (CH2Br2), including oceanic emissions, contribute to stratospheric and tropospheric O3 depletion. Convective transport over tropical oceans could deliver large amounts of these short-lived organic bromine species to the upper atmosphere. High mixing ratios of atmospheric CHBr3 in air masses from the northwest African coast have been hypothesized to originate from the biologically active Mauritanian upwelling. During a cruise into the upwelling source region in spring 2005 the atmospheric mixing ratios of the brominated compounds CHBr3 and CH2Br2 were found to be elevated above the marine background and comparable to measurements in other coastal regions. The shelf waters were identified as a source of both compounds for the atmosphere. The calculated sea-to-air emissions support the hypothesis of a strong upwelling source for reactive organic bromine. However, calculated emissions were not sufficient to explain the elevated concentrations observed in the coastal atmosphere. Other strong sources that could contribute to the large atmospheric mixing ratios previously observed over the Atlantic Ocean must exist within or near West Africa.
    Type: Article , PeerReviewed
    Format: text
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  • 2
    Publication Date: 2018-02-06
    Description: Methyl iodide has been measured during two field campaigns in the Atlantic region in 2002. The first took place in July–August at 2300 m on the island of Tenerife, while the second was a shipborne, east–west crossing of the Tropical Atlantic at 10°N in October–November of the same year. Both campaigns were periodically impacted by dust, advected from Africa in trade winds. Unexpectedly, during these dust events, methyl iodide mixing ratios were observed to be high relative to other times. Backward calculations with the particle dispersion model FLEXPART show the origin of the dust storms as Mauritania and southern Algeria for the ground- and ship-based campaigns, respectively. The dust-laden air traveled from its source above the marine boundary layer to the measurement region. On the basis of the field data correlations and the simulations, we suggest that dust-stimulated emission of methyl iodide has occurred. To test this hypothesis, dust samples were collected from the identified source regions and added to filtered Atlantic seawater. This rapidly produced methyl iodide. Further tests established that the addition of iodide increased the yield and that iodide with H2O2 was greater still. This was found for both sterilized and nonsterilized samples. We conclude that there is an abiotic methyl iodide production mechanism that can occur via substitution, analogous to those in soil, rather than radical recombination. This may occur when dust contacts seawater containing iodide or when marine water vapor condenses on dust containing iodide. This hypothesis appears to be consistent with recent long-term methyl iodide data sets from Tasmania and may help resolve current uncertainties in the iodine cycle.
    Type: Article , PeerReviewed
    Format: text
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  • 3
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    Unknown
    AGU (American Geophysical Union)
    In:  Journal of Geophysical Research: Oceans, 112 . C10006.
    Publication Date: 2019-09-23
    Description: The tropical oceans are a source of reactive bromine to the atmosphere in the form of short-lived brominated methanes as bromoform (CHBr3) and dibromomethane (CH2Br2). Elevated atmospheric concentrations above the tropical oceans are related to oceanic supersaturations of the compounds and especially to upwelling regimes. Although the sources of these brominated gases in the open ocean are not well understood, they have been habitually linked to phytoplankton, especially diatom abundance. Thus according to common assumptions, high concentrations of the brominated trace gases were expected to occur in the biologically active and diatom-rich Mauritanian upwelling. However, contrary to expectations, only low levels were encountered in the upwelling waters, 10.7 (range 5.2–23.8) pmol L−1 CHBr3 and 4.7 (range 3.1–7.0) pmol L−1 CH2Br2, values more typical of open ocean concentrations. The aqueous CHBr3 concentrations were not correlated to high chlorophyll a values or diatom abundances. However, significant correlations existed with low concentrations of marker pigments for diatoms, cyanobacteria, and degradation, suggesting miscellaneous small biological sources of the compound in the upwelling. Air-sea exchange could additionally account for an oceanic source in fresh upwelled waters, while advection of different water masses also influenced the distribution. CHBr3 concentrations were maximized in warm and nitrogen-depleted surface waters, while CH2Br2 was maximized in colder and nitrogen-enriched deeper waters, suggesting that both compounds, at least in part, have different sources and fates.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
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