4.7 Article

Vertical variability of seawater DMS in the South Pacific Ocean and its implication for atmospheric and surface seawater DMS

Journal

CHEMOSPHERE
Volume 78, Issue 8, Pages 1063-1070

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2009.10.054

Keywords

Dimethyl sulfide; Dissolved DMSP; Particulate DMSP; South Pacific; Sea-to-air flux; Mixed layer depth

Funding

  1. Korea Meteorological Administration Research and Development Program [CATER 2007-3204]
  2. Korea Meteorological Administration [CATER 2007-3204] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Shipboard measurements of atmospheric dimethylsulfide (DIMS) and sea surface water DMS were performed aboard the R/V Onnuri across the South Pacific from Santiago, Chile to Fiji in February 2000. Hydrographic profiles of DMS, dissolved dimethylsulfoniopropionate (DMSPd), and particulate DMSPp in the upper 200 m were obtained at 16 stations along the track. Atmospheric and sea surface water DMS concentrations ranged from 3 to 442 pptv and from 0.1 to 19.9 nM, respectively; the mean values of 61 pptv and 2.1 nM, respectively, were comparable to those from previous studies in the South Pacific. The South Pacific Gyre was distinguished by longitudinal-vertical distributions of DMS, DMSPd, and DMSPp, which was thought to be associated with the characteristic modification of biological activities that occurs mainly due to significant change in water temperature. The averaged DMS maximum appeared at 40 m depth, whereas DMSPp and DMSPd maxima coincided with that of dissolved oxygen content at 60-80 m. The sea-to-air fluxes of DMS were estimated to be 0.4-11.3 mu mol d(-1) m(-2) (mean = 2.8 mu mol d(-1) m(-2)). A fairly good correlation between atmospheric DMS and sea-to-air DMS flux indicated that atmospheric DMS concentration was more sensitive to change in physical parameters than its photochemical removal process or surface seawater DMS concentrations. (C) 2009 Published by Elsevier Ltd.

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