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Environmental Radiotracers
John Robbins
Although this is no longer considered a current GLERL
research project, John Robbins continues to work on completing his many
research endeavors in his capacity as a GLERL Scientist emeritus.
Please see the Research Programs page for a list of
current research projects.
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Background and Objectives
The Environmental Radiotracers (ERT) Project employs natural and artificial
radionuclides to identify and model important particle transport processes
in diverse systems including the Laurentian and other Great Lakes, smaller
freshwater bodies, wetlands and coastal marine environments. The project
is an outgrowth of the recognition that, in such systems, many contaminants
and nutrients in the water move in association with inorganic and organic
particles, including plankton species and their remains. Particle-associated
constituents settle through the water column to underlying sediments,
where they may be mixed and resuspended by currents or biological action,
and are ultimately lost by burial in accumulating sediments. Along such
pathways as these, rates of particle transport often can be determined
using particle-associated radionuclides because of their built-in clocks,
relative ease of measurement or accurately known loading histories. Radionuclide
studies often inform development of quantitative process models and this
aspect has been emphasized in the ERT Project.
Since its inception in the early 1980s, this technique-based project
has given particular attention to radiometric dating of sediments. In
addition to the role that sediments play in the regulation of nutrients
and contaminants in aquatic systems, they frequently possess retrievable
records of present and historical changes in ecosystem status and constituent
loads due to natural or human causes. The development, application and
evaluation of radionuclide dating methods address numerous scientific
and public concerns about the changing status of ecosystems, environmental
contamination and global climate change.
Changes in contamination, biological status and physical characteristics
of lakes and coastal marine systems during the past century often lead
to significant changes in the composition of accumulating sediments. Reconstructing
the history of such changes from sedimentary records (paleolimnology)
is an important part of present efforts to understand human impacts on
ecosystems and undertake appropriate remedial strategies. To this end,
it is critical to have reliable and accurate methods of dating sediments.
The Great Lakes Environmental Research Laboratory has been at the forefront
of developing and testing radiotracer methods for sediment dating.
The ERT Project consists of a series of sub-projects with differing duration,
environments and collaborators, which generally share the above objectives.
Sub-projects are a mix of internally-funded activities and formal externally-funded
inter-agency agreements. Over the lifetime of this project there have
been about 30 sub-projects in diverse systems and geographic areas.
Products for this Project
(Publications, Milestone
Reports)
Geographic Coverage
Lake Athabaska (Canada),
Lake Baikal (Russia), Lake Constance (Germany/ Austria/Switzerland), Coeur
D,Alene Lake (Idaho), Florida Bay, Lake George (US/Canada), Great Slave
Lake (Canada), Lake Ladoga (Finland/Russia), Lake Oahe (S. Dakota), Lake
Rockwell (Ohio), Lake Sniardwy (Poland), Lake Tahoe (California/ Nevada),
Lake Winnipeg (Canada), Terrace Lake (Colorado), The Everglades (Florida),
The Gulf of Mexico, The Keweenaw Waterway (Michigan), The Laurentian Great
Lakes (US/Canada).
Formal and Informal Institutional Collaborations (with abbreviations)
AIMS: Australian Institute
of Marine Science, Queensland, Australia
ANL: Argonne National Laboratory, Argonne,
Illinois
CCIW: Canada Centre for Inland Waters, Burlington, Ontario, Canada
CWRU: Case Western Reserve University, Cleveland, Ohio
FWI:
The Freshwater Institute, Winnipeg, Manitoba, Canada
GEO-UM: Department of Geology, University
of Michigan, Ann arbor, MI
GLERL: Great Lakes Environmental Research Laboratory, Ann Arbor, Michigan
GLRD: Great Lakes Research Division, Institute of Science and technology,
Uni-
versity of Michigan, Ann Arbor, MI
GLWI: Great Lakes Water Institute,
U. Wisconsin, Milwaukee, Wisconsin
ILGS: Illinois Geological Survey, Champaign-Urbana,
Illinois
LII: Limnological Institute,
Irkutsk, Russia
MOE-ONT: Ministry of the Environment,
Toronto, Ontario, Canada
MOE-SAS: Ministry of the Environment,
Saskatoon, Saskatchewan, Canada
MTU: Michigan Technological Institute,
Houghton, Michigan
PMEL: Pacific Marine Environmental Research
Laboratory, NOAA, Seattle, WA
SPH-UM: School of Public Health, University
of Michigan, Ann Arbor, MI
SFWMD: South Florida Water Management District,
West Palm Beach, Florida
U. Florida: University of Florida, Gainesville,
Florida
U. Mich.: University of Michigan, Ann
Arbor, Michigan
U. Minn.: University
of Minnesota, Minneapolis, Minnesota
USEPA Duluth: U. S. Environmental Protection
Agency, Duluth, Minnesota
USEPA, LLRS: U. S. Environmental Protection Agency, Large Lakes Research
Station, Grosse Ile, Michigan
USEPA-V: U. S. Environmental Protection Agency, Region V, Enforcement, Chicago,
Illinois
USGS-Atlanta: U. S. Geological Survey,
Atlanta, Georgia
USGS-Denver: U. S. Geological Survey, Denver, Colorado
USGS-Menlo Park: U. S. Geological Survey, Menlo Park, California
USGS-Reston: U. S. Geological Survey, Reston, Virginia
USGS-SP: U. S. Geological Survey, St. Petersburg, Florida
USGS-WH: U. S. Geological Survey, Woods Hole, Massachusetts
U. Constance: University of Constance,
Constance, Germany
U. Joen.: University of Joensuu, Joensuu,
Finland
U. Wrocl.: Dept. of Geological
Sciences, University of Wroclaw, Wroclaw, Poland

Radionuclides Emphasized in the Environmental Radiotracers Project
Lead-210. This naturally occurring radioactive isotope of lead
(t1/2 = 22 years) is part of the uranium decay series that includes radium.
This latter radionuclide occurs widely in soils and rocks and produces
the well-publicized radioactive, chemically inert gas, radon, which leaks
into the atmosphere. Decay of radon (t1/2= 4 days) produces 210Pb, which
is efficiently removed by precipitation, transferred to water bodies and
rapidly incorporated into sediments where it decays on burial. As a result,
a layer of sediment, for example containing half as much 210Pb than at
the surface, would be considered 22 years older than sediments deposited
at the surface and so forth. This simple idea has often proven to work
well in many of the hundreds of studies that have employed the 210Pb method
during the past several decades. However the method is never routine because
sediments may accumulate at variable rates, be subject to near-surface
mixing due to biological or physical processes, and even the rate of delivery
of 210Pb to sediments may vary as a result of physical or geochemical
processes in aquatic systems. Some of the sub-projects described involve
verification of the method, offer approaches to improving its accuracy
and attempt to link 210Pb dating to system specific physical and biogeochemical
processes. In other sub-projects the method is applied to obtain modern
rates of sediment accumulation, rates and ranges of sediment mixing and
residence times of particles in sediment surface mixed layers. In some
cases the 210Pb has been used to date cores where there is an interest
in linking sedimentary records of water body contamination to historical
loading from urban or industrial sources.
Cesium-137. This man-made
radionuclide (t1/2=30 years) was delivered to aquatic systems primarily
through atmospheric fallout of debris from above ground testing of nuclear
weapons mostly in the mid-1960s. In the Great Lakes, 137Cs has attached
to fine particles and cleared out of the water within a few years after
fallout, but small amounts continue to be reintroduced through resuspension
of surface sediments. In cores from selected areas of many lake and coastal
marine sediments as well as wetland soils, there is a clear peak present
at depths corresponding to the fallout maximum in 1963-1964. Thus the
137Cs is useful in verifying sediment cores dates based on 210Pb, but
perhaps more important, 137Cs mimics the behavior of many non-degradable
contaminants circulating in aquatic systems. Since its loading to the
Great Lakes as well as other continental sites, is well-known and 137Cs
is unambiguously and easily determined in sediments, this fallout radionuclide
can be used to track the movements of contaminants through systems during
the past 40 years or so. Some of the sub-projects described below exploit
137Cs to establish or verify sediment accumulation rates while others
exploit its particle-tracking capability to characterize the long-term
fate of contaminants. In the Great Lakes as in may other aquatic systems,
particles that were labeled by 137Cs in the mid sixties are in the process
of being buried and replaced by new, largely uncontaminated particles
from erosion of shoreline of watershed sources. As a result 137Cs is useful
in characterizing mechanisms and times of recovery of water bodies from
past contaminant insults. Another fallout radionuclide mentioned in several
sub-projects is plutonium, primarily the long-lived isotope, 239Pu, (t
1/2 =24,400 years). Plutonium was co-dispersed with 137Cs in nuclear testing
events and deposited essentially in fixed proportion to radiocesium onto
land and water surfaces. Although Pu is chemically dissimilar to cesium,
both elements have labeled suites of particles that have had comparable
transport and fate in the Great Lakes and many other freshwater systems.
Beryllium-7. In contrast with the above radionuclides, naturally
occurring 7Be has a comparatively short half-life (t1/2 = 53 days) and
results from the smashing (spallation) of stratospheric nitrogen and oxygen
nuclei by cosmic rays. Tropospheric concentrations of 7Be and rates of
deposition onto surface water have an annual cycle that depends on a combination
of its seasonally variable efficiency of transfer from the stratosphere
and on regional weather patterns. In the Great Lakes area, the amount
of 7Be transferred to water varies almost sinusoidally each year, with
maximum deposition in May and minimum in December-January. In several
recent sub-projects, the seasonal variability and short half-life of this
particle-tracing radionuclide has been used to characterize transport
processes and their rates on weekly to monthly time scales.
Status of Currently Active Sub-projects
Descriptions of currently active sub-projects are provided below, including
sections on background, recent accomplishments, their significance and
plans for the forthcoming year. In cases where interpretations are provided,
they may not have been subject to a formal peer review process and should
therefore be considered as tentative.
SP-00
Saginaw Bay
SP-1 Lake
Erie Reference Sites
SP- 2 Composition
and Flux of Settling Matter
SP-3
Recent Sedimentation Rates in Lake Ontario
SP-9 Sediment
Focusing in Lake Erie
SP-11 Sediment
Records of Contamination and Biologic Responses in Lake George
SP-16 Gamma
Scan System
SP-33 Copper
Mining Impacts in the Keweenaw Peninsula and Lake Superior
SP-37 Information
Content of Sediments Accumulated in a Wrecked Ship
SP-39 Radionuclides,
Metals and Organic Contaminants in Lake Ladoga Sediments
SP-43 Sediments
in Florida Bay
SP-44 Accumulation
and Mixing of Sediments in Lake Michigan
SP-45
Soil Accretion Rates in South Florida Wetlands
SP-47
Mississippi Basin Carbon Project
SP-48 Episodic
Resuspension Events in Lake Michigan (EEGLE)
SP-49 Vertical
Sediment Transport Models for Lake Tahoe
SP-50
Metal Contaminant Chronology of Recent Sediments near the Great Barrier
Reef, Northern Australia
SP-51
Sedimentary Evidence for Recent Die-Off of Diporeia in Lake Michigan


Last updated: 2006-05-11 mbl
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