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D. U.S. Military: Specific Source Points 

The following listing of US military source points is a summary of the most important contaminated areas out of a total of 150 military facilities now undergoing environmental remediation under the Dept. of DOE Environmental Management program. The Baseline Environmental Management Report (BEMR) cited at the beginning of this part of RADNET Section 11 contains information about all of the following source points. Additional site specific environmental reports will be reviewed and posted as they are received from the Dept. of Energy by RADNET throughout the winter and spring of 1997. For further information go to RADNET section 13, RADLINKS, and surf the many DOE links now available for persons interested in evaluating weapons production related anthropogenic radioactivity source points. Site specific environmental reports are available from the DOE upon request.
 
Argonne National Laboratory

A research facility located within the confines of the Idaho National Engineering Laboratory covering 1 sq. mile and consisting of 40 buildings and associated discharge ditches, waste ponds, cooling towers, etc. "The primary mission of the Argonne National Laboratory West was to support liquid metal reactor research and development of the Integral Fast Reactor Program (IFRP)" (BEMR, pg. Idaho-4), a fast breeder reactor which has now been canceled. The site of current spent nuclear fuel and waste treatment, including pyroprocessing, a type of fuel reprocessing. Little or no information is currently available about ANL as a past or present plume source point. ANL is the likely location of some french drains; the BEMR indicates total life cycle environmental restoration and waste management costs are $357,482,000. Included in remediation efforts are radioactive wastes storage tanks and "waste water handling/disposal systems such as ditches, ponds, pits, and drains" (BEMR, pg. Idaho-7). Dick Lindsay, Director of Information, informs RADNET that the Argonne National Laboratory not only is not "top secret," as previously described by the Editor of RADNET, but that "it is not associated with the military nor has it been except in trivial or peripheral ways. ... If you are a U.S. citizen and wish to tour you may do so, and that has always been the case! Top secret indeed." For a non-top secret installation, not associated with weapons production activities, ANL has certainly run up a fairly large life-cycle environmental waste restoration and waste management bill.
 
Brookhaven National Laboratory

A U.S. DOE research and development laboratory within 2,265 acres located 75 miles east of New York City in Upton, Long Island. This laboratory contains 24 separate facilities and "approximately 80 areas of interest" (BEMR pg. New York-7) which are the subject of DOE environmental remediation efforts or have been identified for further study. "The principal environmental medium of concern at Brookhaven National Laboratory is ground water. Because the Laboratory is situated over a sole-source aquifer providing potable water for Long Island, the Environmental Protection Agency placed it on the National Priorities List in 1989. ... Contaminants of concern ... that may have migrated through soils, surface water, and related transport mechanisms into the aquifer ... include metals, organic compounds, and radionuclides such as tritium and cesium-137. Contamination occurred as a result of accidental spills and/or past operating practices." (BEMR pg. New York-6). The Brookhaven site is the location of two nuclear research reactors: the High Flux Beam Reactor and the Brookhaven Medical Research Reactor. The High Flux Beam Reactor is currently the topic of intense public EPA and DOE scrutiny due to the discovery of a tritium plume allegedly originating from leaks in the 68,000 gallon spent fuel pool in the reactor's lower level. Levels of tritium have been recorded as high as 651,000 picocuries per liter, or 32 times the U.S. drinking water standard of 20,000 picocuries per liter. (Lexis-Nexis: EPA update 2/6/97). This specific plume allegedly bears no relationship to a number of other tritium plumes in the Brookhaven area groundwater, all of which are supposedly below the EPA's drinking water standard and probably originate from earlier uncontained releases of radionuclides and mixed wastes. The Brookhaven facility is an example of a small DOE facility with multiple source points of contamination overlying an important aquifer and located in a highly populated area. Uncontained releases of contaminants, including ethylene dibromide (EDB), originating decades ago have the potential for significant impact on drinking water supplies on Long Island; the multiple Brookhaven plumes have resulted in the recent closing of hundreds of private wells and the transfer of these residences to public water supply. The BEMR report focuses on 24 specific sources of contamination grouped in five "operable units" as well as a number of aboveground and underground waste storage tanks and cesspools. Life cycle remediation costs are estimated at $866,778,000 excluding the costs of disposing of spent fuel at the Savannah River facility. Brookhaven may be an example of where the High Flux Beam Reactor spent fuel pool leak may be used as a scapegoat to avoid the acknowledgment of the extensive uncontained releases of radioactivity and volatile chemicals of the past. No reference is made in the BEMR to a radiocesium source point, probably located in the biology forest in the southeastern part of the facility that was installed almost 40 years ago for the purpose of irradiating the forest and studying the resulting radiobiological effects. A number of the following citations reference this important and intense above ground installation, the current location and environmental impact of which are unknown.

Flaccus, E., Armentano, T.V., and Archer, M. (1974). Effects of chronic gamma radiation on the composition of the herb community of an oak-pine forest. Radiat. Bot. 14. 263-271.

Franz, E.H. and Woodwell, G.M. (1973). Effects of chronic gamma irradiation on the soil algal community of an oak-pine forest. Radiat. Bot. 13. 323-329.

Gschenaur, S.E. and Woodwell, G.M. (1974). The soil micro-fungi of a chronically-irradiated oak-pine forest. Ecology. 55. 1004-1016.

Holt, B.R. (1972). Radiosensitivity and distribution of common macro-fungi in a chronically irradiated oak-pine forest. Radiat. Bot. 12. 339-342.

U. S. Nuclear Regulatory Commission. (February 1999). NRC report on Brookhaven reactor. U.S. NRC, Washington, DC. http://www.nrc.gov/OPA/reports/brookhvn.htm.

Wagner, R.H. (1966). Herbaceous recolonization of the Brookhaven irradiated forest: the first three years. Radiat. Biol. 6. 561-565.

Woodwell, G.M. and Rebuck, A.L. (1967). Effects of chronic gamma radiation on the structure and diversity of an oak-pine forest. Ecol. Monogr. 37. 53-69.
 
Fernald, Ohio (Feed Materials Production Center)

This small facility (9 plants, 1,148 acres) was established in 1951 for the purpose of processing uranium into a finished product suitable for weapons production. While no DOE high-level wastes are located at this facility, extensive contamination of the groundwater, soil, and air resulted from the careless operation of this plant in the early years of the production of almost a half million metric tons of uranium metal. Waste disposal in pits and surface storage areas as well as in drums and silos resulted in huge quantities of mixed wastes containing as much as 5,000 metric tons of uranium (Makhijani, et. al., Nuclear Wastelands, 1995, pg. 214) This site also contains radium-226 wastes, as well as thorium and a variety of mixed wastes including volatile organic compounds (VOCs), PCB's and trichloroethane. Of particular concern has been the huge quantities of uranium contaminated particulates released to the air during operation of this facility. Political pressures have resulted in Fernald's position among the top ranked DOE remediation sites; the result of the pressures to clean up this facility are unclear. Makhijani (Nuclear Wastelands, 1995) reports the Minimum Additive Wastes Stabilization (MAWS) program results in extensive "off/gas" contamination from the vitrification process as well as the creation of "approximately half a million metric tons of radioactive marbles that would result from even partial conversions of Fernald's on-site contaminated materials." (pg. 215).

Defense Nuclear Facilities Safety Board. (June 16, 1993). Health and safety factors associated with DOE's management and direction of environmental restoration management contracts. Recommendation 93-4 to the Secretary of Energy.

Defense Nuclear Facilities Safety Board. (September 29, 1994). Fernald Environmental Management Project - Uranium/thorium interim storage safety review trip report (September 20-21, 1994). Memorandum for G. W. Cunningham, Technical Director. Makhijani, A. (July 7, 1989). Release estimates of radioactive and non-radioactive materials to the environment by the Feed Materials Production Center 1951-85. Institute for Energy and Environmental Research, Takoma Park, Maryland.

Makhijani, A. (October, 1996). Radioactivity in the Fernald neighborhood. Science for Democratic Action. An IEER (Institute for Energy and Environmental Research) publication. 5(3). pp. 16.

U. S. Department of Energy. (February, 1991). Closure plan for the Feed Materials Production Center: Fernald's main priority is cleanup. U.S. DOE, Washington, D.C.
 
Hanford Reservation, Washington State 

In January 1943 the Hanford Site was established as the nation's first full time plutonium production facility. As part of the Manhattan project, plutonium production reactors were built along the Columbia River (100 Area); processing plants and associated facilities were constructed on a plateau in the center of the site (200 Areas); and fuel fabrication facilities were constructed in the southern component of the reservation (300 Area). The total size of the Hanford site is 560 sq. miles; the site is located in the southeastern part of the state of Washington in an isolated and desiccated area; the Columbia River forms the sites eastern boundary. An excellent site map is contained in the BEMR on page Washington 5; this report includes a summary of the stages of plutonium production at Hanford, including the fabrication of plutonium from uranium, fuel irradiation which converted small amounts of uranium to plutonium, and chemical processing in which the irradiated fuel elements were chemically processed to extract the plutonium. In the early days of operation of the Hanford facility, large amounts of uncontained radioactive wastes of every description were disposed of in the natural environment. Some effluents went directly into the Columbia River; other effluents went into burial trenches, partially lined underground vaults and other surface locations. Extensive use of deep well and shallow well injection technologies resulted in the disposal of unknown quantities of radioactive wastes in subsurface geological formations. By 1972 eight of nine production reactors had been shut down and most fuel separation facilities had also ceased operations. A fast flux test facility at the Hanford Reservation continues to be on hot standby (the facility is cooled by liquid sodium); the Clinton administration is considering restarting this facility to produce tritium for use in future nuclear weapons production. Radioactive wastes in contaminated material and liquid by-products are stored in 1,391 locations on this Reservation; "environmental contamination is found in surface and subsurface soils ... liquids (principally liquid low-level waste effluents) have been discharged into the soils and has contaminated 520 sq. km. of ground water ... the chemical processing of irradiated fuels generated the largest volume of Hanford's wastes" (BEMR, pg. Washington 6-7). Total life cycle remediation costs are estimated at $50,208,297,000. The Oak Ridge National Laboratory Integrated Data Base reports the Hanford Reservation inventory of high-level waste as of Jan. 1, 1996 at 347,900,000 Ci. (Also see additional comments on missing U.S. military (DOE) high-level wastes in part 14 of this section.)

The Panel on Radioactivity in the Marine Environment (1971) prepared an incomplete list of Annual discharges of radioactivity from the Hanford Reactor Operations to the Pacific Ocean (Ci). (p.28) part of which is included below.
 
Year Beta 32P 51Cr 65Zn 239Np
1960 93,000 Ci 6,200 Ci 310,000 Ci 14,000 Ci 26,000 Ci
1961 - 11,000 310,000 16,000 24,000
1962 - 4,700 240,000 11,000 11,000
1963 - 4,400 320,000 10,000 18,000
1964 - 4,400 320,000 16,000 -
1965 - 4,000 290,000 18,000 -
1966 - 3,300 160,000 8,000 -
1967 - 4,400 224,000 15,000 -

The Panel on Radioactivity in the Marine Environment (1971) prepared an incomplete list of Annual average concentrations of several radionuclides in Columbia River Water, 1966. (p.29) part of which is included below.
 
Radionuclides Richland (pCi/liter)
24Na 2,600
32P 140
51Cr 3,600
64Cu 1,400
65Zn 200
76As 420
90Sr 1
131I 18
239Np 770
Agnew, S.F. and Corbin, R.A. (August 1998). Analysis of SX Farm leak histories -- historical leak model. LA-UR-96-3537. Chemical Science and Technology Division, Los Alamos National Laboratory.

Beasley, T.M. (1986). Nickel-63 in Columbia River sediments below the Hanford Reservation. J. Environ. Radioactivity. 4. 1-10.

Beasley, T.M., Ball, L.A. and Andrews, J.E. (1981). Hanford-derived plutonium in Columbia River sediments. Science. 214(20). 913-915. Beasley, T.M., Ball, L.A., Andrews, J.E. and Halverson, J.E. (1980). 243,244Cm in Columbia River sediments. Nature, 287(5783). 624-625.


Benson, A.B. and Shook, L. (1985). Blowing in the wind: Radioactive contamination of the soil around the Hanford Nuclear Reservation. Hanford Education Action League, Spokane, WA.


Connor, T. (1986). Hot water: Groundwater contamination at the Hanford Nuclear Reservation. Hanford Education Action League, Spokane, WA.


Defense Nuclear Facilities Safety Board. (October 11, 1990). Safety at Single-Shell Hanford Waste Tanks. Recommendation 90-7 to the Secretary of Energy pursuant to Section 312(5) of the Atomic Energy Act of 1954, as amended.


Defense Nuclear Facilities Safety Board. (July 19, 1993). Hanford Waste Tanks Characterization Studies. Recommendation 93-5 to the Secretary of Energy pursuant to 42 U.S.C. 2286a(5) Atomic Energy Act of 1954, as amended.

Defense Nuclear Facilities Safety Board. (October 1997). Review of the Hanford spent nuclear fuel project. DNFSB/TECH-17. Washington, D.C.

Emery, R.M. and McShane, M.C. (1980). Nuclear waste ponds and streams on the Hanford Site: an ecological search for radiation effects. Health Physics. 38. 787-809.

Eslinger, P.W., Huesties, L.R., Maughan, A.D., Miley, T.B. and Walters, W.H. (1994). Data Compendium for the Columbia River Comprehensive Impact Assessment. PNL-9785, Pacific Northwest Laboratory, Richland, Washington.

Gerber, M. S. (1992). On the home front: the cold war legacy of the Hanford nuclear site. University of Nebraska Press, Lincoln. 312 pp.

Martin, T. (Winter, 1993). Waste by any other name ... Deciding what goes into Hanford Grout. Perspective. Hanford Education Action League, Hanford, Washington. pg. 8-9.

Miley, T.B., and Huesties, L.R. (1995). List of currently classified documents relative to Hanford operations and of potential use in the Columbia River Comprehensive Impact Assessment. January 1, 1973-June 20, 1994. PNL-10459, Pacific Northwest Laboratory, Richland, Washington.

Napier, B.A., Batishko, N.C., Heise-Craff, D.A., Jarvis, M.F. and Synder, D.F. (1995). Identification of contaminants of concern. PNL-10400, Pacific Northwest Laboratory, Richland, Washington.

Napier, B.A., Harper, B.L., Lane, N.K., Strenge, D.L. and Spivey, R.B. (1996). Human scenarios for the screening assessment: Columbia River Comprehensive Impact Assessment. DOE/RL-96-16-a, U. S. Department of Energy, Richland, Washington.

Robertson, D.E., Silker, W.B., Langford, J.C., Petersen, M.R. and Perkins, R.W. (1973). Transport and depletion of radionuclides in the Columbia River. In: Radioactive Contamination of the Marine Environment. Report No. IAEA-SM-158/9. IAEA, Vienna. 141-158.

Saleska, S. and Makhijani, A. (July, 1990). To process or not to process: the PUREX question: the alternatives for the management of N-Reactor irradiated fuel at the U.S. Department of Energy's Hanford Nuclear Reservation. Report prepared for the Hanford Education Action League. Institute for Energy and Environmental Research, Takoma Park, Maryland.

Sanger, S.L. (1989). Hanford and the Bomb: An Oral History of World War II. Living History Press, Seattle, Washington.

Scheibe, T. and Yabusaki, S. (1993). Scaling of flow and transport behavior in heterogeneous groundwater systems. PNL-SA-25636. EOS Trans. AGU. 74(43) 251.

Schmel, G.A. (1978). Airborne plutonium-239 and americium-241 transport measured from the 125-m Hanford meteorological tower. In: Selected environmental plutonium research reports of the Nevada Applied Ecology Group. White, M.G. and Dunaway, P.B. eds. Las Vegas, NV. 707-722.

Serber, R., (1992). The Los Alamos Primer. University of California Press, Berkeley, California.

Shook, L. and Benson, A. The storm of Hanford's radioactive iodine, "Ominous implications". The Hanford Journal, 5, 1-3.

U. S. Department of Energy. (1995). Hanford Site environmental report for calendar year 1994. Department of Energy, Richland Operations Office, Richland, Washington. U. S. Department of Energy. (August, 1995). Registration of Hanford Site Class V underground injection wells. Revision 1. Report no. DOE/RL--88-11-Rev.1. NTIS order no. DE95017148. Westinghouse Hanford Co., Richland, Washington. 59 pp. U. S. Department of Energy. (February 20, 1996). Request for proposals (RFP) No. DE-RP06-96RL13308: Tank Waste Remediation System (TWAS). Department of Energy, Richland Operations Office, Richland, Washington. Washington State Department of Ecology, U. S. Environmental Protection Agency and U.S. Department of Energy. (1994). Hanford Federal Facility Agreement and Consent Order. Document No. 89-10, Rev. 3 (The Tri-Party Agreement), Ecology, Olympia, Washington.

Woodruf, R.K., Hanf, R.W. and Lundgren, R.E. (1993). Hanford Site environmental report for calendar year 1992. PNL-8682. Pacific Northwest Laboratory, Richland, Washington.

Wurstner, S.K. and Freshley, M.D. (December 1994). Predicted impacts of future water level decline on monitoring wells using a ground-water model of the Hanford site. Report Number PNL-10196 UC-903. Prepared for the U.S. Department of Energy by Pacific Northwest Laboratory, Richland, Washington.

Idaho National Engineering Laboratory 

The Oak Ridge National Laboratory Integrated Data Base reports the Idaho National Engineering Laboratory inventory of high-level waste as of Jan. 1, 1996 at 51,600,000 Ci. (Also see additional comments on missing U.S. military (DOE) high-level wastes in part 11 of this section; on site uncontained inventories of weapons production high-level waste and spent nuclear fuel are likely to be much higher than the amount noted in the ORNL data base.)

Environmental Science and Research Foundation. (August 1996). Idaho National Engineering Laboratory Site Environmental Report for Calendar Year 1995. Environmental Science and Research Foundation Report Series, Number 014 (ISSN 1089-5469). Environmental Science and Research Foundation, Idaho Falls, ID.

Environmental Science and Research Foundation. (September 1996). In Summary: Idaho National Engineering Laboratory Site Environmental Report for Calendar Year 1995. Environmental Science and Research Foundation Report Series, Number 015 (ISSN 1089-5469). Environmental Science and Research Foundation, Idaho Falls, ID. Ghuman, G.S. (1993). Distribution of Antimony-125, Cesium-137, and Iodine-129 in the soil-plant system around a nuclear fuel reprocessing plant. J. Environ. Radioactivity, 21, 161-176.
 
1987 I.N.E.L. Total activity (mean) 125Sb 1041.7 Bq/m2

Halford, D.K. et al. (February 1981). Radionuclide Concentrations in Waterfowl using a Liquid Radioactive Disposal Area and the Potential Radiation Dose to Man. Health Physics. 40. p. 173-181.
 
Unknown, before 1980 Idaho National Engineering Laboratory Waterfowl 137Cs 5,400,000 pCi/kg (200,000 Bq/kg fresh weight)
Unknown, before 1980 Idaho National Engineering Laboratory Waterfowl 51Cr 1,300,000,000 pCi/kg fresh weight (4,816,000 Bq/kg)

Lockheed Martin Idaho Technologies Company. (August 1995). A comprehensive inventory of radiological and nonradiological contaminants in waste buried in the subsurface disposal area of the INEL RWMC during the years 1952-1983. INEL-95/0310, Rev. 1. Idaho National Engineering Laboratory, Idaho Falls, ID.
 
Lawrence Livermore National Laboratory
Lawrence Livermore National Laboratory. Environmental Report 1995. (September 3, 1996). Howard L. Lentzner, Editor. UCRL-50027-95, Distribution Category UC-702. http://www.llnl.gov/saer. 
  • One of a number of US DOE nuclear weapons research laboratories, the two sites comprising the LLNL, while not probable locations of a significant quantity of missing military high-level wastes, are the subject of federally mandated environmental monitoring reports as a result of weapons research and testing activities. 
  • "Typical gross alpha activity (median value) for the LLNL [air monitoring] perimeter network is 2.2 x 10-13 Bq/mL (2.2 x 10-7 Bq/m3...) typical gross beta activity (median value) for the LLNL perimeter is 4.1 x 10-10 Bq/mL (4.1 x 10-4 Bq/m3)" (pg. 4-5). 
  • Soil and sediment monitoring produced the following average values: 
    • "Background levels of 239+240Pu are given as .22 x 10-3 Bq/gm (.22 Bq/Kg)." (pg. 10.5) 
    • "The slightly higher values near the Livermore site have been attributed to historic operations, which included the operation of solar evaporators for plutonium-containing liquid waste in the south east quadrant... LLNL no longer operates solar evaporators or any other open air treatment of plutonium containing waste, nonetheless, 239+240Pu from historic operations is carried off site by resuspension of soil by wind." (pg. 10.5) 
    • 239+240Pu levels are noted as follows: Livermore Valley .09 x 10-3 Bq/dry g (.09 Bq/Kg) median; 1.1 Bq/Kg maximum; Livermore Water Reclamation Plant (LWRP) 3.5 Bq/Kg median; 25 Bq/Kg maximum; Livermore site sediments .07 Bq/Kg median; 3.3 Bq/Kg maximum. (pg. 10.5). 
    • While most plutonium is attributed to stratospheric weapons testing fallout, "an estimated 1.2 x 109 Bq (32 mCi) plutonium released to the sewer in 1967 and first observed in soils near LWRP during the early 1970's again were detected at LWRP sampling locations." (pg. 10.5). One related location was identified in a 1993 EPA sampling "as containing more than the EPA industrial preliminary remediation goal (PRG) of 0.37 Bq/g (10 pCi/g); the location contained up to 11.5 pCi/g of 239/240Pu." (pg. 10.12). 
    • 137Cs levels are noted as follows: Livermore Valley soils 2.6 x 10-3 Bq/dry g (2.6 Bq/Kg) median; 8.1 Bq/Kg maximum; LWRP and Livermore site sediment contamination is noted as slightly lower than the off site levels of contamination for this weapons fallout radionuclide. (pg. 10.6). 
  • This detailed environmental report, along with providing excellent circa 1995 baseline data on levels of anthropogenic radioactivity in a California location upwind of most weapons testing sites, contains an extensive list of LLNL Environmental Protection Department publications which provide extensive documentation of the history of weapons testing contamination and monitoring at this location, as well as an excellent general bibliography. 

Gallegos, G. (1995). Surveillance monitoring of soils for radioactivity: Lawrence Livermore National Laboratory 1976 to 1992. Health Physics. 69(4). pg. 487-493.

Sullivan, T.J., Nasstrom, J.S. and Greenly, G.D. ARAC: Early phase dose assessment for the DOE FRMAP. UCRL--101355-Rev.1, DE90 001052. Lawrence Livermore National Laboratory.
Los Alamos National Laboratory

This 43 square mile national laboratory was established in 1943 to design develop and test nuclear weapons. The BEMR report (1996) cited at the beginning of this part of RADNET section 11 notes "an important function of the laboratory has been processing plutonium metal and alloys from nitrates solution feedstock provided by other production facilities ... 1945 - 1978. Other operations included reprocessing nuclear fuel, processing polonium and actinium, and producing nuclear weapons components" (BEMR vol. 3, pg. New Mexico 26). "A major source of environmental contamination was waste being discharged into the environment or buried in material disposal areas ... residual contamination may exist in more than 7 million cubic meters, primarily soils and sediments ... in approximately 2100 potential release sites" (BEMR vol. 3, pg. New Mexico 27). The BEMR report divides major environmental restoration activities into six field units, with a detailed description of restoration activities in each unit. Total life cycle cost estimates for this location are $623,650,000. Excellent maps are included in the BEMR summary.

Graf, William L., (1994). Plutonium and the Rio Grande: Environmental Change and Contamination in the Nuclear Age. Oxford University Press, New York, Oxford.

Haagenstad, H.T., Gonzales, G., and Suazo, I. L., (November, 1993). Radioactive liquid waste treatment facility: environmental information document. DOE Contract W7405ENG36. Sup.Doc.Num. E 1.99:DE95003618. NTIS Order Number DE95003618. Primary Report Number: LA-UR--94-1507. 115pp. Hakonson, T.E. and Bostick, K.V. (1976). Cesium-137 and Plutonium in Liquid Waste Discharge Areas at Los Alamos. In Radioecology and Energy Resources. Edited by Cushing, C.E. Jr. Special Publication 1, Ecological Society of America. Dowden, Hutchinson & Ross, Stroudsburg, PA. pg. 40-48.

Hanson, W.C. (1975). Ecological considerations of the behavior of plutonium in the environment. Health Physics, 28, 529-537.

Lane, L.J., Purtymun, W.D., and Becker, N.M. (1985). New Estimating Procedures for Surface Runoff, Sediment Yield, and Contaminant Transport in Los Alamos County, New Mexico. Los Alamos National Laboratory Report LA-10335-MS, UC-11. Los Alamos National Laboratory. Los Alamos, N.M.

Nyhan, J.W., Drennon, B.J., Abeele, W.V., Wheeler, M.L., Purtymun, W.D., Trujillo, G., Herrera, W.J., and Booth, J.W. (1985). Distribution of Plutonium and Americium Beneath a 33-Year-Old Liquid Waste Disposal Site. Journal of Environmental Quality. vol. 14. pg. 501-9.

Purtymun, W.D., Johnson, G.L., and John, E.C. (1966). Distribution of Radioactivity in the Alluvium of a Disposal Area at Los Alamos, New Mexico. U. S. Geological Survey Professional Paper 550-D. U. S. Geological Survey, Washington, D.C.

Purtymun, W.D. (1971). Plutonium in Stream Channel Alluvium in the Los Alamos Area, New Mexico. (USAEC Report No. LA-4561). Los Alamos, NM: Los Alamos Scientific Laboratory.

Purtymun, W.D. (1974). Storm Runoff and Transport of Radionuclides in DP Canyon, Los Alamos County, New Mexico. Los Alamos National Laboratory Report LA-5744. Los Alamos National Laboratory. Los Alamos, N.M.

Purtymun, W.D., Peters, R.J., Buhl, T.E., Maes, M.N., and Brown, F.H. (1987). Background concentrations of Radionuclides in Soils and River Sediments in Northern New Mexico, 1974-1986. Los Alamos National Laboratory Report LA-11134-MS, UC-11. Los Alamos National Laboratory. Los Alamos, N.M.

Purtymun, W.D., Peters, R.J., and Maes, M.N. (1990). Transport of Plutonium in Snowmelt Runoff. Los Alamos National Laboratory Report LA-11795-MS, UC-902. Los Alamos National Laboratory. Los Alamos, N.M.

Shroyer, J.A. (1998). Peering into Los Alamos; Secret Mesa:  Inside Los Alamos National Laboratory. John Wiley & Sons, Inc., New York, NY.

Stoker, A., Ahlquist, A.J., Mayfield, D.L., Hanson, W.R., Talley, A.D., and Purtymun, W.D. (1981). Radiological Survey of the Site of a Former Radioactive Liquid Waste Treatment Plant (TA-45) and the Effluent Receiving Areas of Acid, Pueblo, and Los Alamos Canyons, Los Alamos, New Mexico. Los Alamos National Laboratory and U.S. Department of Energy Report LA-8890-ENV, UC-70. Los Alamos National Laboratory, Los Alamos, N.M.


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