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Träfflista för sökning "WFRF:(Oeberg Gunilla) "

Search: WFRF:(Oeberg Gunilla)

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1.
  • Bengtson, Per, et al. (author)
  • Possible roles of reactive chlorine II: assessing biotic chlorination as a way for organisms to handle oxygen stress
  • 2013
  • In: Environmental Microbiology. - : Wiley-Blackwell. - 1462-2912 .- 1462-2920. ; 15:4, s. 991-1000
  • Research review (peer-reviewed)abstract
    • Natural formation of organically bound chlorine is extensive in many environments. The enzymes associated with the formation of chlorinated organic matter are produced by a large variety of organisms. Little is known about the ecological role of the process, the key question being: why do microorganisms promote chlorination of organic matter? In a recent paper we discuss whether organic matter chlorination may be a result of antagonistic interactions among microorganisms. In the present paper we evaluate whether extracellular microbial formation of reactive chlorine may be used as a defence against oxygen stress, and we discuss whether this process is likely to contribute to the formation of chlorinated organic matter. Our analysis suggests that periodic exposure to elevated concentrations of reactive oxygen species is a common denominator among the multitude of organisms that are able to enzymatically catalyse formation of reactive chlorine. There is also some evidence suggesting that the production of such enzymes in algae and bacteria is induced by oxygen stress. The relative contribution from this process to the extensive formation of chlorinated organic matter in natural environments remains to be empirically assessed.
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2.
  • Gustavsson, Malin, et al. (author)
  • Organic Matter Chlorination Rates in Different Boreal Soils: The Role of Soil Organic Matter Content
  • 2012
  • In: Environmental Science and Technology. - : American Chemical Society. - 0013-936X .- 1520-5851. ; 46:3, s. 1504-1510
  • Journal article (peer-reviewed)abstract
    • Transformation of chloride (Cl-) to organic chlorine (Cl-org) occurs naturally in soil but it is poorly understood how and why transformation rates vary among environments. There are still few measurements of chlorination rates in soils, even though formation of Cl-org has been known for two decades. In the present study, we compare organic matter (OM) chlorination rates, measured by Cl-36 tracer experiments, in soils from eleven different locations (coniferous forest soils, pasture soils and agricultural soils) and discuss how various environmental factors effect chlorination. Chlorination rates were highest in the forest soils and strong correlations were seen with environmental variables such as soil OM content and Cl- concentration. Data presented support the hypothesis that OM levels give the framework for the soil chlorine cycling and that chlorination in more organic soils over time leads to a larger Cl-org pool and in turn to a high internal supply of Cl- upon dechlorination. This provides unexpected indications that pore water Cl- levels may be controlled by supply from dechlorination processes and can explain why soil Cl- locally can be more closely related to soil OM content and the amount organically bound chlorine than to Cl- deposition.
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3.
  • Oeberg, Gunilla, et al. (author)
  • Transformation of Chloride to Organic Chlorine in Terrestrial Environments: Variability, Extent, and Implications
  • 2012
  • In: Critical reviews in environmental science and technology. - : Taylor andamp; Francis: STM, Behavioural Science and Public Health Titles. - 1064-3389 .- 1547-6537. ; 42:23, s. 2526-2545
  • Research review (peer-reviewed)abstract
    • Chloride (Cl-in) is a key component in a number of biogeochemical risk assessment models and, as a rule, these models assume that Cl-in behaves conservatively in soil. However, this assumption is challenged by the growing number of studies on natural formation-mineralization of organically bound chlorine (Cl-org) in terrestrial environments. The authors synthesized and scrutinized previously reported transformation rates of Cl-in to Cl-org in terrestrial environments to assess whether the process is of sufficient size to impact risk assessment models significantly. Their conclusion is that there is increasing evidence that considerable amounts of Cl-in are transformed to Cl-org in or on plants and that the process consistently runs at relatively high rates. The findings imply that risk assessment models that include uptake-transport of Cl-in by vegetation are likely to be influenced by the transformation of Cl-in to Cl-org in or on vegetation. The review confirms previous observations that transformation rates in soils depend on a combination of a number of factors such as concentration or deposition of Cl-in, organic matter content, nutrient availability, redox, and season. The review reveals that there seems to be at least two pools of Cl-org in the terrestrial environment: one with slow transformation rates, low mobility, and with a comparably low chlorine-to-carbon ratio (leaves, litter, and bulk-soil), and a smaller pool with considerably higher transformation rates, higher mobility and higher chlorine-to-carbon ratios (organic matter in through fall and soil leachate). Formation of chlorinated organic matter has a strong biotic component, implying that models built on physicochemical parameters (e.g., sorption and Kd values) are insufficient to predict movement and fate of Cl-36. The study clearly demonstrates that it is necessary to develop reliable rate estimates and methods that enable a deeper understanding of how and why the Cl-in is transformed to Cl-org and how this influences transport, distribution, and fate of Cl-36 in different environments.
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