4.7 Article

Carbon mineralization and oxygen dynamics in sediments with deep oxygen penetration, Lake Superior

期刊

LIMNOLOGY AND OCEANOGRAPHY
卷 57, 期 6, 页码 1634-1650

出版社

WILEY
DOI: 10.4319/lo.2012.57.6.1634

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资金

  1. National Science Foundation (NSF) [OCE 0961720]
  2. NSF Ocean Sciences (OCE) [0825633, 0927512, 0825600]
  3. Minnesota Sea Grant
  4. University of Minnesota Duluth start-up funds
  5. Water Resources Science Block Grant
  6. University of Minnesota Duluth Physics Department summer fellowships
  7. Undergraduate Research Opportunities Program
  8. Directorate For Geosciences [0961720, 0825600, 0825633] Funding Source: National Science Foundation
  9. Directorate For Geosciences
  10. Division Of Ocean Sciences [0927512] Funding Source: National Science Foundation
  11. Division Of Ocean Sciences [0961720, 0825600, 0825633] Funding Source: National Science Foundation

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To understand carbon and oxygen dynamics in sediments with deep oxygen penetration, we investigated eight locations (160-318-m depth) throughout Lake Superior. Despite the 2-4 weight percent organic carbon content, oxygen penetrated into the sediment by 3.5 to > 12 cm at all locations. Such deep penetration is explained by low sedimentation rates (0.01-0.04 cm yr(-1)), high solubility of oxygen in freshwater, and a shallow (similar to 2 cm) bioturbation zone. In response mainly to oxygen variations in the bottom waters, the sediment oxygen penetration varied seasonally by as much as several centimeters, suggesting that temporal variability in deeply oxygenated sediments may be greater than previously acknowledged. The oxygen uptake rates (4.4-7.7 mmol m(-2) d(-1), average 6.1 mmol m(-2) d(-1)) and carbon mineralization efficiency (similar to 90% of deposited carbon) were similar to those in marine hemipelagic and pelagic sediments of comparable sedimentation rates. The reactivity of organic carbon was found to decrease with age similarly to the power-law documented in marine environments. The burial flux of carbon into the deep sediment (0.7 mmol m(-2) d(-1)) was 2.5% of the previously estimated primary production. Maximum volume-specific carbon degradation rates were 0.3-1.5 mmol cm(-3) d(-1); bioturbation coefficient near the sediment surface was 3-8 cm(2) yr(-1). These results indicate that carbon cycling in large freshwater systems conforms to many of the same trends as in marine systems.

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