HR: 1340h
AN: B53C-1007 [Abstracts]
TI: Carbon Mineralization Pathways and Early Diagenesis in Lake Erie Sediments
AU: * O Neill, A H
EM: andrewo@uwindsor.ca
AF: Great Lakes Institute, University of Windsor, 401 Sunset Ave, Windsor, ON N9B 3P4
Canada
AU: Crowe, S A
EM: sacrowe@uwindsor.ca
AF: Great Lakes Institute, University of Windsor, 401 Sunset Ave, Windsor, ON N9B 3P4
Canada
AU: Crowe, S A
EM: sacrowe@uwindsor.ca
AF: Earth and Planetary Sciences, McGill University, 3450 University St., Montreal, QC H3A 2A7
Canada
AU: Song, Z
EM: songc@uwindsor.ca
AF: Great Lakes Institute, University of Windsor, 401 Sunset Ave, Windsor, ON N9B 3P4
Canada
AU: Mucci, A
EM: alm@mcgill.ca
AF: Earth and Planetary Sciences, McGill University, 3450 University St., Montreal, QC H3A 2A7
Canada
AU: Sundby, B
EM: bjorn.sundby@mcgill.ca
AF: Earth and Planetary Sciences, McGill University, 3450 University St., Montreal, QC H3A 2A7
Canada
AU: Fryer, B J
EM: bfryer@uwindsor.ca
AF: Great Lakes Institute, University of Windsor, 401 Sunset Ave, Windsor, ON N9B 3P4
Canada
AU: Fowle, D A
EM: fowle@uwindsor.ca
AF: Great Lakes Institute, University of Windsor, 401 Sunset Ave, Windsor, ON N9B 3P4
Canada
AB:
In spite of the long-standing paradigm whereby organic matter degradation proceeds by redox reactions that consume oxidants
in the order of free energy yield, diagenesis in marine and fresh water sediments often yield different results. The reasons
for this are the highly variable absolute and relative abundances of electron acceptors and the different microbial
populations found in freshwater environments. As contaminant availability and subsequent impact on aquatic ecosystems are
directly linked to these transformations, it is important to understand the most important degradation pathways and their
rates.
To this end we have conducted chemical analyses of Lake Erie sediment pore-waters and a preliminary characterization of the
vertical distribution of microbiological populations. Sediments were collected at four locations in the Central and Eastern
basins of Lake Erie during cruises of the R/V LIMNOS in May and June of 2004 respectively. High-resolution vertical profiles
of several redox-active species (O2, Fe2+, Mn2+, Fe3+ and S2-) have been obtained by voltammetry using Au/Hg amalgam
micro-electrodes. These are the first high-resolution pore-water profiles obtained for multiple redox species using Au/Hg
amalgam microelectrodes in the Great Lakes.
These profiles show oxygen depletion to levels below detection (5 uM) at depths that range from <1 to 6 mm below the
sediment-water interface. Frequently, there is up to 1 cm separation between the depth at which O2 became undetectable and
the depth of the first measurable Mn2+. The vertical concentration profiles of Mn2+ and Fe2+ are highly variable between
stations and seem to be related to the local bathymetry. Alternatively this variability may be related to the abundance of
solid phase Mn and Fe at these sites. The presence of voltammetric peaks measured between -0.5 and -0.6 V, that are often
attributed to dissolved organic Fe (III) species, could be produced as part of a strategy by Fe reducing microorganisms to
render solid phase Fe (III) bioavailable. Mn2+ voltammetric peaks were shifted to potentials more negative than the -1.53 to
-1.55 mV commonly observed in marine pore waters. This shift is consistent with previous studies in freshwaters and has been
ascribed to Mn2+ complexation by organic ligands (e.g. Luther et al, 2003). However, this shift may be due to analytical
artifacts associated with using a solid state Ag/AgCl reference electrode in low ionic strength solutions. Measurable
sulphide in the first 5 cm below the sediment-water interface is sporadic which suggests that sulphate reduction occurs in
micro-environments locally enriched in organic carbon.
Preliminary cultivation-independent, microbiological analyses have revealed 16s rDNA clones that are closely related to known
species capable of enzymatic reduction of Fe(III) and the dechlorination of organic compounds (e.g. Anaeromyxobacter
dehalogenans). These organisms were vertically dispersed within several different core sections suggestive of an intriguing
tie between diagenetic reactions and anthropogenic organic compound degradation in these sediments. Coupling high-resolution
voltammetry and spatially resolved genomic tools to investigate the controls on sediment pore water chemistry holds a
promising future for elucidating the controls on early diagenesis in freshwater ecosystems.
DE: 1030 Geochemical cycles (0330)
DE: 1045 Low-temperature geochemistry
DE: 1065 Trace elements (3670)
DE: 0330 Geochemical cycles
DE: 0394 Instruments and techniques
SC: Biogeosciences [B]
MN: 2004 AGU Fall Meeting