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Dissolved iron (II) in the Baltic Sea surface water and implications for cyanobacterial bloom development

Breitbarth, Eike (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
Gelting, J. (author)
Walve, J. (author)
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Hoffmann, L. J. (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Institutionen för växt- och miljövetenskaper,Department of Chemistry,Department of Plant and Environmental Sciences
Turner, David R., 1951 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
Hassellöv, Martin, 1970 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry
Ingri, J. (author)
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 (creator_code:org_t)
2009
2009
English.
In: Biogeosciences. ; 6, s. 2397-2420
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Iron chemistry measurements were conducted during summer 2007 at two distinct locations in the Baltic Sea (Gotland Deep and Landsort Deep) to evaluate the role of iron for cyanobacterial bloom development in these estuarine waters. Depth profiles of Fe(II) were measured by chemiluminescent flow injection analysis (CL-FIA) and reveal several origins of Fe(II) to the water column. Photoreduction of Fe(III)-complexes and deposition by rain are main sources of Fe(II) (up to 0.9 nmol L−1) in light penetrated surface waters. Indication for organic Fe(II) complexation resulting in prolonged residence times in oxygenated water was observed. Surface dwelling heterocystous cyanobacteria where mainly responsible for Fe(II) consumption in comparison to other phytoplankton. The significant Fe(II) concentrations in surface waters apparently play a major role in cyanobacterial bloom development in the Baltic Sea and are a major contributor to the Fe requirements of diazotrophs. Second, Fe(II) concentrations up to 1.44 nmol L−1 were observed at water depths below the euphotic zone, but above the oxic anoxic interface. Finally, all Fe(III) is reduced to Fe(II) in anoxic deep water. However, only a fraction thereof is present as ferrous ions (up to 28 nmol L−1) and was detected by the CL-FIA method applied. Despite their high concentrations, it is unlikely that ferrous ions originating from sub-oxic waters could be a temporary source of bioavailable iron to the euphotic zone since mixed layer depths after strong wind events are not deep enough in summer time.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

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