U.S. Department of the Interior
U.S. Geological Survey
| Project Goals | Background | Research Plan | Product Plans | Collaboration & Partnership | Project Schedule | Progress to Date | For More Information |
High concentrations of methyl-mercury
(CH3Hg+), a substance toxic to both animals
and humans, recently have been measured in a number of top
predators (including panthers and game fish) native to the
Florida Everglades.
As part of a larger research group investigating
the mercury (Hg) cycle in south Florida, our work has focused
on the microbiological and geochemical processes that control
CH3Hg+ degradation in Everglades peat-sediment.
Field measurements of CH3Hg+ degradation
rates are currently being provided to ecosystem managers. From
this and other field data, predictive Hg cycle models are being
constructed to aid in making informed decisions regarding hydrologic
and nutrient management strategies that may influence the Everglades
Hg cycle.
The objective of this research is to provide ecosystem
managers with CH3Hg+ degradation rate data
from a number of study sites that represent a diversity of hydrologic
and nutrient regimes common to the Everglades. Further, our focus
is on better understanding the microbial and geochemical controls
regulating CH3Hg+ degradation. At present,
little is known regarding the specific factors influencing this
process in natural systems.
The methylated form of Hg (i.e. CH3Hg+)
is the most readily bioaccumulated Hg species in the food chain
as a result of its affinity for protein groups. The primary source
of Hg to the Everglades is from particle bound atmospheric deposition.
Particle bound inorganic Hg+2 is transported to the
sediment where it is methylated by sulfate reducing bacteria (SRB).
In addition to methylating Hg, sediment bacteria can also demethylate
CH3Hg+, although much less is known about
this reverse reaction. Both SRB and methane producing bacteria
(MPB) are thought to be involved in this process. The sum of both
the methylation and demethylation reactions determines if a particular
location is a net source or sink of CH3Hg+.
The microbial degradation of CH3Hg+
may proceed by two known pathways, namely, methyl-cleavage (MC)
(producing Hg+2 and CH4) or oxidative demethylation
(OD) (producing Hg+2 , CH4 and CO2).
By measuring the carbon based end-products (i.e. CH4
and CO2), the fraction of CH3Hg+
degradation attributable to each of these pathways may be assessed
at a particular location and/or depth .
Bacteria that degrade CH3Hg+
via MC may also posses the capacity to further reduce Hg+2
to volatile Hg0. However, it is unknown if this reduction
is associated with conditions favoring OD. Since the formation
of volatile Hg0 potentially represents a permanent
loss of Hg from the system, a clear understanding of the processes
controlling both MC and OD is needed.
The Everglades Water Conservation Areas are large
sections of wetlands currently being used as nutrient removal
zones for water draining the Everglades Agricultural Area. To
the extent that nutrients affect the complex microbial dynamics
in water and sediments, their direct and indirect impact on bacteria
involved in the Hg cycle is of primary interest.
Our work is divided into both a field and laboratory
component. One year of research has been completed. The specific
areas of current and future investigations are outlined below.
While high concentrations of 14CH3Hg+
have been measured in some Everglades animal species, the concentrations
in the sediment are extremely low (> 0.01 ng * cc wet sediment).
Therefore, the amount of 14CH3Hg+
needed to produce detectable end-products is well above these
natural background levels. Hence, measurements to date represent
upper estimates of potential rates. An alternative method for
extrapolating to in-situ rates is currently being explored (see
below).
As previously indicated, experiments with radiolabeled
14CH3Hg+ at or below natural
concentrations (i.e. tracer experiments) are not currently feasible.
However, an alternative approach for the assessment of in-situ
rates is currently being explored. This approach entails measuring
the degradation rate over a large range of 14CH3Hg+
concentrations, and extrapolating results to predict in-situ
degradation rates. Preliminary laboratory experiments with this
method suggest that the rate of CH3Hg+ degradation
is a linear function of concentrations over two orders of magnitude
(see graph). With an order for custom-made high specific activity
14CH3Hg+ pending, we expect
to repeat these types of measurements at all sites and decrease
our lowest addition by another order of magnitude. Thus, this
approach appears promising and will be used during upcoming field
work.
At a number of select sampling
sites, sediment cores are sectioned into three to five discrete
2 cm horizons, within hours of sample collection. Sub-samples
from each horizon are transferred into crimp sealed serum vials,
purged with N2 gas, and injected with radiolabeled
14CH3Hg+. After incubating for
a number of days, end-products (14CH4 and
14CO2 ) are measured via gas proportional
counting. The relative amounts of these compounds are a direct
indication of 14CH3Hg+ degradation
via MC or OD, respectively. Degradation rates are assessed with
respect to both sediment depth and site location.
The affect of nutrients (NO3-, PO4-3,
NH4+) and SO4-2 on
the degradation of 14CH3Hg+ is
assessed by amending parallel sets of incubation samples with
these substrates and processing as described above. Likewise,
specific microbial inhibitors of both SRB and MPB are used to
determine the relative contribution of these microbial groups
to 14CH3Hg+ degradation.
In a series of laboratory experiments we will attempt to isolate
specific bacteria (SRB and MPB), from Everglades sediment, capable
of degrading 14CH3Hg+. We will
concentrate on isolating strains that degrade 14CH3Hg+
by either MC or OD exclusively. We will then be able to explore
the bacterial mechanisms by which degradation proceeds under each
pathway.
In additional laboratory experiments the fate of Hg after 14CH3Hg+
degradation will be explored. Vapor phase Hg0 is collected
on gold traps by flushing the head-space of previously incubated
samples. The concentration of Hg0 is then assayed by
cold vapor atomic fluorescence spectroscopy. Preliminary work
in this area using whole sediment was recently completed, while
work with bacterial isolates is pending.
|
| Kinetic Experiment:14CH3Hg+ degradation rate versus 14CH3Hg+ spike concentration plotted on log-log axis. X-axis is extended to the range typical for in-situ 14CH3Hg+ concentrations. Dashed line represents linear least-squares fit. Resulting r2 = 0.988 [larger image] |
Product Plans:
In addition to the pool of ancillary data available
from the larger Hg study group, we are working particularly closely
with Dr. Cindy Gilmour (Academy of Natural Science, MD) and Dr.
David Krabbenhoft (USGS, Madison Wisconsin). Measurements of Hg-methylation
are conducted by Dr. Gilmour in parallel with our demethylation
rate field study. Both of these parameters are needed to model
net 14CH3Hg+ production dynamics.
Dr. Krabbenhoft is working with us on assessing the fate of Hg
following 14CH3Hg+ degradation.
The Hg0 analysis is conducted in his laboratory.
Results from the first year of field and laboratory data suggest
that the potential rate of
14CH3Hg+ degradation increases
with distance from the Everglades Agricultural Area. Increased
NO3- levels decreased degradation rates,
while increased PO4-3 had no affect . Both
SRB and MPB were responsible for
14CH3Hg+
degradation. Preliminary experiments suggest that very little
(>> 0.01%) of liberated Hg+2 produced as a
result of 14CH3Hg+ degradation
is reduced to volatile Hg0 .
Collaboration & Partnership:
For more information contact:
Ronald S. Oremland
U.S. Geological Survey
Menlo Park, CA 94025
(415) 329-4442
Related information:
SOFIA Project: Bacterial demethylation of methylmercury in the South Florida Ecosystem
U.S. Department of the Interior, U.S. Geological Survey
This page is: http://sofia.usgs.gov/publications/fs/bactdem/print.html
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Last updated: 10 November, 2004 @ 03:43 PM(TJE)