-------
Douglas K. Sauter Potter Rarwh
Grand Vallfty
City Springs
Grand Valay f^-'P- i. --- -
Keven Wielan
Jacobsl
gfettoment Cn^K.
XB Spring 300 yds
SGZ^b^NofSGZ
EOfSGZ
N
8 Water SatnpSng Locations
tOCATKSHMAP
Map is not to scale
COLORADO
OARFIELO
COUNTY
Figure 3. Project RUI.tSON sampling tocations for May 2W)5.
-------
2.3.3 Conclusions
Tritium concentrations in water samples collected onsite and offsite are consistent with those of past
studies at the RULISON Test Site. In general, the current level of tritium in shallow wells at the
RULISON site cannot be distinguished from the rain-out of naturally produced tritium augmented
by, perhaps, a small amount of residual global "fallout tritium" remaining from nuclear testing in the
1950s and 1960s. All routine samples were analyzed for presence of gamma-ray emitting
radionuclides.
2.4 Sampling at Project RIO BLANCO, Colorado
History
Project RIO BLANCO, a joint government-industry test designed to stimulate natural gas flow, was
conducted under the Plowshare Program. The test was conducted on May 17, 1973, at a location
between Rifle and Meeker, Colorado. Three explosives with a total yield of 99 KT were emplaced at
1,780, 1,920, and 2,040 m (5,840, 6,299, and 6,693 ft) depths in the Ft. Union and Mesa Verde
formations. Production testing continued until 1976 when cleanup and restoration activities were
completed. Tritiated water produced during testing was injected to 1,710 m (5,610 ft) in a nearby
gas well.
2.4.1 Sample Collection
Sampling was conducted on May 12-13, 2005, and locations are shown in Figure 4. The routine
sampling locations included four springs, four surface, and five wells, three of which are located
near the cavity. At least two of the wells (Wells RB-D-01 and RB-D-03) are suitable for monitoring
because they were down gradient and would indicate possible migration of radioactivity from the
cavity.
2.4.2 Water Analysis Results
Gamma-ray spectral analysis results indicated that no man-made gamma-ray emitting radionuclides
were present in any offsite samples. Three of the 15 samples collected were above the MDC for
enriched tritium and none were above the MDC using the conventional method (see Table 4, page
12).
2.4.3 Conclusions
Tritium concentrations in water samples collected onsite and offsite are consistent with those of past
studies at the RIO BLANCO Site. No radioactive materials attributable to the RIO BLANCO test
were detected in samples collected in the offsite areas during May 2005. All samples were analyzed
for presence of gamma-ray emitting radionuclides.
10
-------
Meeker
Black 9ut>hur
B-1 Equity
Creek#1
Fawn Crank 8400' DavwiBtMm
RB-D-03
| R&-W-01
I Fawn Creek SOT/ Downstream
| Fawn Crook 500* Upstream
Fawn Creak 6800' Upstrean
"". Fawn Creak Spr. <3
RbBknoa
N
Ma Sampling Locfitians
Sufaoe Ground Zero
Map Is not to scale
LOCATION NAP
RtoHlura
COUMTV
Figure 4. Project RIO BLANCO sampling locations for May 2005.
II
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Analysis Results for Water Samples Collected at the RIO BLANCO Site - May 2005
TABLE 4
Sample
Location
B-l Equity Camp
Brennan Windmill
CER#I Black
Sulphur
CER #4 Black
Sulphur
Fawn Creek # 1
Fawn Creek #3
Fawn Creek 500'
Upstream
Fawn Creek 6800'
Upstream
Fawn Creek 500'
Downstream
Fawn Creek 8400'
Downstream
Johnson Artesian
Well
WellRB-D-01
Well RB-D-03
Well RB-S-03
Well RB-W-OI
Well RB-D-01 R
Well RB-S-03 R
Well RB-D-03 R
WellRB-W-01 R
Collection
Date
5/13/05
5/12/05
5/13/05
5/13/05
5/12/05
5/12/05
5/12/05
5/12/05
5/12/05
5/12/05
5/12/05
5/12/05
5/12/05
5/12/05
5/12/05
5/12/05
5/12/05
5/12/05
5/12/05
Enriched Tritium
pCi/L ± 2 SD (MDC)
21±7.1 (11)
27 ± 6.4 (9 8)
10 ±6.0 (9.5)
-.53 ±5 7(a) (9 5)
Tritium00
pCi/L ± 2 SD (MDC)
-38±185(0) (305)
38±186(1) (305)
-95±184(a) (305)
105±187(a) (305)
52±186(n) (305)
114±187(a) (305)
109 ±187°" (305)
66±186W (305)
43±186W (305)
-109±183(" (305)
-8I±I84W (305)
1I4±187<" (305)
62±l86(a) (305)
-47±184W (305)
100±187(il) (305)
Gamma
Spectrometry00
pCi/L (MDC)
ND (5.0)
ND (4.7)
ND (4.6)
ND (4.4)
ND (4.9)
ND (4.8)
ND (4.4)
ND (4.2)
ND (4.3)
ND (5.0)
ND (4.8)
ND (4.0)
ND (4.7)
ND (4.7)
ND (5.0)
(a) Indicate results are less than MDC (enriched or conventional method).
(b) Value in parenthesis represents '"Cs MDC (pCi/L).
ND Non-detected.
MDC Minimum detectable concentration
R Rinse sample.
12
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2.5 Sampling at Project GASBUGGY, New Mexico
History
Project GASBUGGY was a Plowshare Program test co-sponsored by the U.S. AEC and El Paso
Natural Gas Co., conducted near Gobernador, New Mexico, on December 10, 1967. A nuclear
explosive with a 29-KT yield was detonated at a depth of 1,290 m (4,232 ft) to stimulate a low
productivity natural gas reservoir. Production testing was completed in 1976 and restoration
activities were completed in July 1978.
The principal aquifers near the test site are the Ojo Alamo Sandstone, an aquifer containing non-
potable water located above the test cavity, and the San Jose formation and Nacimiento formation.
Both surficial aquifers contain potable water. The flow regime of the San Juan Basin is not well
known, although it is likely that the Ojo Alamo Sandstone discharges to the San Juan River 50 miles
northwest of the Gasbuggy site. Hydrologic gradients in the vicinity are downward, but upward gas
migration is possible (Chapman and Hokett, 1991).
2.5.1 Sample Collection
Annual sampling at Project GASBUGGY was completed during June 14-16, 2005. All of the
routine sampling locations were collected except for Bubbling Spring which was dry (see
Figure 5) and EPNG-10-36 which was plugged in 2003.
2.5.2 Water Analysis Results
Tritium concentrations of water samples collected onsite and offsite are consistent with those of past
studies at the GASBUGGY Site.
Well EPNG 10-36 has yielded tritium activities between 100 pCi/L in 2000 to 0.05 ± 4 in 2003. In
2003, Well EPNG 10-36 was plugged due to the severe deterioration of the well casing. DOE will
drill several wells in the near future, placed in strategic location designed to intercept migration of
radionuclides, if they should occur. The migration mechanism and route are not currently known,
although an analysis by Desert Research Institute indicated two feasible routes, one through the
Printed Cliffs sandstones, and the other one through the Ojo Alamo sandstone, one of the principal
aquifers in the region (Chapman and Hokett, 1991).
Gamma-ray spectral analysis results indicated that no man-made gamma-ray emitting radionuclides
were present in any onsite and offsite samples above the MDC. Tritium concentrations at all
locations except for three were below the MDC. The sampling locations that had a tritium
concentration above the MDC were Cedar Springs of 19 ± 5.8 pCi/L, LaJara Creek 25 ±5.8 pCi/L
and Well 23 South 17 ±6.0 pCi/L (see Table 5, page 15).
13
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To Bloomfield &
Farmington
1 Pond N. of
Well 30.3.32.343N
Well 30.3.32.343N
La Jara Creek
1
Bubbling
Springs
Jicarilla Well 1
EPNG Well
Cedar Springs
Cave Spnngs
Arnold Ranch Spring
Arnold Ranch Well
Lower Burro
Canyon
Well 28.3.33.233S
Gobernador
Old
Store
LOCATION MAP
Surface Ground Zero
Water Sampling Locations
Not a Sampling Location
Map is not to scale
RIO
ARRIBA
COUNTY
NEW
MEXICO
Figure 5. Project GASBUGGY sampling locations for June 2005.
14
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2.5.3 Conclusions
Tritium concentrations of water samples collected onsite and offsite are consistent with those of past
studies at the GASBUGGY Site.
Analysis Results for Water Samples Collected at the GASBUGGY Site - June 2005
TABLE 5
Sample
Location
Arnold Ranch
Spring
Bubbling Springs
Cave Springs
Cedar Springs
La Jara Creek
Lower Burro
Canyon
Pond N. of Well
30 3.32.343
Wei IEPNG- 10-36
JicarillaWell I
Well 28 3.33.233
(South)
Well 30.3.32 343
(North)
Windmill #2
Arnold Ranch Well
Collection
Date
6/15/05
6/14/05
6/15/05
6/16/05
6/15/05
6/15/05
6/16/05
6/16/05
6/15/05
6/15/05
6/16/05
6/15/05
6/15/05
Enriched Tritium
pCi/L±2SD (MDC)
9.5±6.7(a) (11)
19 ±5.8 (9.0)
25 ±5.8 (8.9)
5 8 ±5.4(" (9 0)
17±60 (93)
Tritium00
pCi/L ± 2 SD (MDC)
38±173W (284)
-26±l72(a) (284)
32±173(1) (284)
-21±172<" (284)
-85±171(a) (284)
Gamma Spectrometry00
pCi/L (MDC)
ND (4.9)
No sample, spring dry
ND (4.9)
ND (4.9)
ND (4.9)
ND (5.0)
ND (5.0)
No Sample Well
Plugged
ND (4.9)
ND (5.0)
No Sample Windmill
disconnected
ND (4.8)
ND (4.7)
(a) Indicate results are less than MDC (enriched or conventional method).
(b) Value in parenthesis represents '"Cs MDC (pCi/L).
ND Non-detected.
MDC Minimum detectable concentration.
15
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2.6 Sampling at Project GNOME, New Mexico
History
Project GNOME, conducted on December 10,1961, near Carlsbad, New Mexico, was a
multipurpose test emplaced at a depth of 370m (1,216 ft) in the Salado salt formation. The explosive
yield was slightly-more-than 3-K.T. Oil and gas are produced from the geologic units below the
working point. The overlying Rustler formation contains three water-bearing zones: brine located at
the boundary of the Rustler and Salado formations, the Culebra Dolomite which is used for domestic
and stock supplies, and the Magenta Dolomite which is above the zone of saturation (Chapman and
Hokett, 1991). The ground water flow is generally to the west and southwest.
Radioactive gases were accidentally vented following the test. In 1963, USGS conducted a tracer
study involving injection of 20 Ci tritium, 10 Ci 137Cs, 10 Ci 90Sr, and 4 Ci I3II in the Culebra
Dolomite zone; using Wells USGS 4 and 8. During remediation activities in 1968-69, contaminated
material was placed in the test cavity and the shaft up to within 7 ft of the surface. More material
was slurried into the cavity and drifts in 1979. A potential exists for discharge of this slurry to the
Culebra Dolomite and to Rustler-Salado brine. Potentially, this may increase as the salt around the
cavity compresses, forcing contamination upward and distorting and cracking the concrete stem and
grout.
2.6.1 Sample Collection
Annual sampling at Project GNOME was completed during June 21-23, 2005. The routine sampling
sites, depicted in Figure 6, includes ten monitoring wells in the vicinity of surface GZ; the municipal
supplies at Loving and Carlsbad, New Mexico.
2.6.2 Water Analysis Results
No tritium activity was detected in the Carlsbad municipal supply or the Loving Station well. An
analysis by Desert Research Institute (Chapman and Hokett, 1991) indicates that these sampling
locations, which are on the opposite side of the Pecos River from the Project GNOME site, are not
connected hydrologically to the site and, therefore, cannot become contaminated by Project GNOME
radionuclides.
Tritium results greater than the MDC were detected in water samples from four of the 12 sampling
locations in the immediate vicinity of GZ. Tritium activities in wells LRL-7, USGS-4, DD-1 and
USGS-8 ranged from 761 ± 183 (LRL-7) to 3.46 x 107± 1.63 x 104(DD-1) pCi/L. Well DD-1
collects water from the test cavity; Well LRL-7 collects water from a side drift; and Wells USGS-4
and USGS-8 were used in the radionuclide tracer study conducted by the USGS. None of these wells
are sources of potable water (See Table 6).
In addition to tritium, l37Cs and 90Sr concentrations were observed in samples from Wells DD-1,
LRL-7, and USGS-8, while 90Sr activity was detected in Well USGS-4 as in previous years (see
Table 6). No tritium was detected in the remaining sampling locations, including Well USGS-1,
which the DRI analysis (Chapman and Hokett, 1991) indicated is positioned to detect any migration
of radioactivity from the cavity. All other tritium results were below the MDC.
16
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Carlsbad City
Well 7 •
Carlsbad
Loving City
Well 2 •
HS Well 8
PHSWelMO
PHS Well 6
Surface Ground Zero
Water Sampling Locations
Map is not to scale
EDDY
COUNTY
LOCATION MAP
Figure 6. Program GNOME sampling locations for June 2005.
17
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2.6.3 Conclusion
No radioactive materials attributable to the GNOME Test were detected in samples collected in the
offsite areas during June of 2005.
Analysis Results for Water Samples Collected at the GNOME Site - June 2005
TABLE 6
Sample
Location
Well 7 City
Well 2 City
Well PHS 6
Well PHS 8
Well PHS 9
Well PHS 10
Well USGS 1
Well USGS 4
Well USGS 8
J Mobley Ranch
WellDD-1
Well LRL-7
WellDD-1 R
Well USGS 4 R
Well USGS 8 R
Well LRL-7 R
Collection
Date
6/22/05
6/22/05
6/22/05
6/22/05
6/23/05
6/23/05
6/21/05
6/21/05
6/21/05
6/22/05
6/23/05
6/21/05
6/23/05
6/21/05
6/21/05
6/21/05
Enriched Tritium
pCi/L±2SD (MDC)
4.5±5 4(a) (8.8)
7.7±6 0°" (9.7)
10±65 (10)
Tritium
pCi/L±2SD (MDC)
I73±170(a) (274)
I21±169(" (274)
63±168(a) (274)
5.8±167W (274)
3.l2xl04±517 (274)
3.65x1 0"±555 (274)
3.46xl07±1.63xl04 (274)
761±183(a) (274)
86± 169(a) (274)
.00±167W (274)
IIO±169(a) (274)
-17±166(>) (274)
Gamma Spectrometry™
pCi/L (MDC)
ND (4.9)
No sample-well plugged
ND (4.9)
ND (5.0)
ND (4.6)
ND (5.0)
ND (4.4)
ND (1.7)
89±14 (1.9)
ND (4.7)
6. 12x1 0s ±9.24x10" (3980)
26±4.6 (1.9)
(a) Indicate results are less than MDC (enriched or conventional method).
(b) Value in parenthesis represents '"Cs MDC (pCi/L)
ND Non-detected.
MDC Minimum detectable concentration.
R Rinse sample.
18
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REFERENCES
Chapman & Hockett, 1991. Evaluation ofGroundwater Monitoring at Offsite Nuclear Test Areas,
Las Vegas, NV, Desert Research Institute, University of Nevada System, Report DOE/NV/10845-07.
Final rule on Dec. 7, 2000. Code of Federal Regulations, Vol. 65, Title 40, Parts 9, 141, and 142,
December 7, 2000, National Primary Drinking Water Regulations; Radionuclides: Final Rule;
(40CFR9/141/142).
A Guide for Environmental Radiological Surveillance at U.S. Dept. of Energy Installations, July
1981, Office of Operational Safety Report. Las Vegas, NV: U.S. Department of Energy; DOE/EP-
0023.
Johns, F., et al. 1979. Radiochemical and Analytical Procedures for Analysis of Environmental
Samples. Las Vegas, NV: U.S. Environmental Protection Agency; EMSL-LV-0539-17-1979.
Offsite Environmental Monitoring Report Radiation Monitoring Around Nuclear Test Areas,
Calendar Year 1992. EPA 600/R-947209.
19
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GLOSSARY OF TERMS
Background Radiation
The radiation in man's environment, including cosmic rays and radiation from naturally-occurring
and man-made radioactive elements, both outside and inside the bodies of humans and animals. The
usually quoted average individual exposure from background radiation is 125 millirem per year in
mid-latitudes at sea level.
Curie (Ci)
The basic unit used to describe the rate of radioactive disintegration. The curie is equal to 37 billion
disintegrations per second, which is the equivalent of 1 gram of radium. Named for Marie and Pierre
Curie who discovered radium in 1898. One microcurie (u,Ci) is 0.000001 Ci.
Isotope
Atoms of the same element with different numbers of neutrons in the nuclei. Thus I2C, 13C, and MC
are isotopes of the element carbon, the numbers denoting the approximate atomic weights. Isotopes
have very nearly the same chemical properties, but have different physical properties (for example
12C and "C are stable, I4C is radioactive).
Enrichment Method
A method of electrolytic concentration that increases the sensitivity of the analysis of tritium in
water. This method is used for selected samples if the tritium concentration is less than 700 pCi/L.
Minimum Detectable Concentration (MDC)
The smallest amount of radioactivity that can be reliably detected with a probability of Type I and
Type II errors at 5 percent each (DOE 1981).
Offsite
Areas exclusive of the immediate Test Site Area.
Type I Error
The statistical error of accepting the presence of radioactivity when none is present. Sometimes
called alpha error.
Type II Error
The statistical error of failing to recognize the presence of radioactivity when it is present.
Sometimes called beta error.
20
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Appendix A
Typical MDC Values for Gamma Spectroscopy
(100 minute count time)
Geometry*
Matrix
Volume
Marinelli
Water
3.5 liter
Model
Density
Units
430G
l.Og/ml
pCi/L
Isotope
MDC
Isotope
MDC
Be-7
K-40
Cr-51
Mn-54
Co-57
Co-58
Fe-59
Co-60
Zn-65
Nb-95
Zr-95
4.56E+01
4.92E+01
5.88E+01
4.55E+01
9.65E+00
4.71E+00
1.07E+01
5.38E+00
1.24E+01
5.64E+00
9.06E+00
Ru-106
Sn-113
Sb-125
1-131
Ba-133
Cs-134
Cs-137
Ce-144
Eu-152
Ra-226
U-235
Am-241
4.76E+01
8.32E+00
1.65E+01
8.28E+00
9.16E+00
6.12E+00
6.43E+00
7.59E+01
2.86E+01
1.58E+01
1.01E+02
6.60E+01
Disclaimer
The MDA's provided are for background matrix samples presumed to contain no known analytes and no
decay time. All MDA's provided here are for one specific *Germanium detector and the geometry of
interest. The MDA's in no way should be used as a source of reference for determining MDA's for any other
type of detector. All gamma spectroscopy MDA's will vary with different types of shielding, geometries,
counting times and decay time of sample.
21
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Appendix B
Standard Operating Procedures for the Center
for Radioanalysis & Quality Assurance
RQA-302 Standard Operating Procedures of Gamma-Ray Detector Systems
RQA-602 Tritium Enrichment Procedure
RQA-603 Standard Operating Procedure for 89Sr and 90Sr in Water, Air Filters and Milk
RQA-604 Standard Operating Procedure of Convention Tritium in Water
RQA-606 Analysis of Plutonium, Uranium and Thorium in Environmental Samples by Alpha
Spectroscopy
Standard Operating Procedures for the Center for
Environmental Restoration, Monitoring & Emergency Response
CER-203 Standard Operating Procedure for the Long-Term Hydrological Monitoring Program
CER-804 Sampling Equipment Decontamination Procedures
22
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