WATER SAMPLING AND ANALYTICAL RESULTS FROM THE SULPHUR BANK MERCURY MINE SUPERFUND SITE, LAKE COUNTY, CALIFORNIA1 By John R. Benham2 Abstract. The Sulphur Bank Mercury Mine is an inactive open pit mine located in Lake County, California. The mine occupies 120 acres and is adjacent to Clear Lake. The mine's pit has been flooded by runoff and thermal spring activity creating a 23 acre acid mine water pond (Herman Pit). Mercury has been found at the mine site, in Clear Lake waters, and in fish in Clear Lake. Due to this mercury contamination and the mine's proximity to Clear Lake, the Sulphur Bank Mercury Mine was added to the National Priorities List in 1990 by USEPA (Superfund). In 1991, the USEPA requested that the U.S. Bureau of Mines perform sampling and chemical analysis on waters taken from the mine pit, monitor wells, thermal spring waters, and surface waters of Herman Pit and Clear Lake. Field work began in August, 1992. An underwater hot spring sampler was designed and constructed by U.S. Bureau of Mines personnel. Along with sonar, it was first used to sample ambient water and thermal springs in both Herman Pit and Clear Lake. In Herman Pit, at the mine site, the water has a pH of 3. An inflatable hypalon boat was used as the sampling platform on this chemically harsh environment. standard USEPA water sampling protocol was observed during all sampling events. All samples were split. One sample set was chemically analyzed within 24 hours of sampling. For these analyses, a portable laboratory was utilized. The other set of sample splits were sent to USEPA's analytical laboratory in Las Vegas, Nevada. All analytical results suggest that mercury occurs in waters at the mine site. U.S. Bureau of Mines analytical results suggest that water at the mine site and springs within Clear Lake contribute to mercury concentrations within Clear Lake. USEPA analytical data suggests that mercury is confined to the mine site and not in Clear Lake. Mercury is natural to the area as shown by the presence of the Sulphur Bank Mercury Mine. Background concentrations of mercury in the Clear Lake area would undoubtedly be much higher than background readings found elsewhere. 1Paper presented at the 10th National Meeting of the American Society for Surface Mining and Reclamation, Spokane, Washington, May 16-19, 1993. Publication in these proceedings does not preclude authors from publishing their manuscripts, whole or in part, in other publication outlets. 2John R. Benham is a Hydrologist with the U.S. Bureau of Mines, Western Field Operations Center, Spokane, WA 99202 165 :Introduction springs are underwater in Herm- an Pit and in Clear Lake. Her- The Sulphur Bank Mercury man Pit is acidic at pH 3. Mine Superfund site is located Theref.ore, a remote sampling in Lake County, California device was needed. The U.S. (Figure 1). The Superfund site Bureau of Mines designed, engi- is the result of over 100 years neered, and assembled an under- of uncontrolled deposition of water spring sampler (Figure mining/milling wastes. The 2) • site was placed on the United States Environmental Protection The underwater sampler is Agency's (USEPA) National Pri- composed of a standard one-li- orities List (NPL) in 1990. In ter teflon bailer with check 1991, Region IX of the U.S. EPA valves at both ends. The lower charged the U.S. Bureau of end has a low flow variable Mines with reconnaissance level speed submersible pump at- sampling of surface water, tached. Temperature probes are ground water, and underwater positioned at both ends with thermal springs in order to the lower probe used to find determine if mercury at the the spring while the upper site poses a threat to the en- probe indicates when the bailer vironment. In order to do this is full of hydrothermal fluid it was necessary to design a after pumping. To assist in sampling device that is capable finding the spring, a video of acquiring representative camera and light are housed in samples from underwater thermal underwater cases and are at- springs. tached by adjustable arms to the bailer. Also, a high defi- nition sonar bottom profiler Objectives was used. One of the objectives of this on-site work was to deter- Herman Pit. Three hydrothermal mine if mercury exists in sur- spring samples and one surface face and spring waters. If water sample (ambient) were mercury exists, what form does taken from Herman Pit using the it occur; how is it currently remote underwater sampler (Fig- being deposited; and has the ure 3) . A duplicate of the mining process exacerbated the ambient sample was taken for mercury? To achieve these ob- quality control. Two one-li- jectives, the U.S. Bureau of ter volumes were taken at each Mines sampled and analyzed sur- location. Splits of all sam- face waters and various under- ples were sent to EPA' s Las water and surface hydrothermal Vegas contract laboratory (ICF springs. Technology Incorporated). The splits consisted of a one-liter volume for metals and a 500-ml Water Sampling volume for anions. Underwater Hydrothermal Springs Clear Lake. Two underwater Underwater spring sampler. The spring and two surface water majority of the hydrothermal samples (ambient) were taken 166 --- ------ 'lit... Interstate 5 34miles -~Cl Rattiesnake Island ! CLEAR LAKE \ (Oaks Arm) • 0 1 MILE Index Map Figure 1. -- Location of the Sulphur Bank Mine Superfund site. 167 Stainless steel Cable cable complex Carabiner Check valve - Temperature Probe No. 2 Teflon--1 bailer Video camera in underwater housing\ 12 volt lamp in underwater housing Adjustable support arms Check valve - Submersible pump Figure 2. -- Sketch of the underwater hot spring sampler. 168 0 1000 FEET SB-HP-SW-001 - 39° 15' "' SB-HP-US-001 ~ -9- SB-WELL-8 SB-HP-US-002 SB-HP-AWS-001A,B Clear Lake SB-POND-002 SB-CL-TS-001 SB-POND-001 - 39° 00' ~ SB-CL-AWS-002 SB-BL-001 0 5 10 MILES 122° 45' Figure 3. -- Sample location map. 169 from Clear Lake using the re- chemical parameters was obtain- mote underwater sampler (Figure ed for each water sample. The 3). Splits of one of the un- physical parameters include pH, derwater springs and one of the Eh, temperature, specific con- ambient water samples were sent ductivity, total dissolved sol- to EPA's Las Vegas laboratory. ids (TDS), and field dissolved oxygen (DO). All were per- formed in the field at each surface Hydrothermal Spring sample site and in the labora- tory prior to analysis. This Off-site Spring. One surface was done to ensure an addition- thermal spring found on a small al level of quality assurance. island also was sampled (Figure 3). One split was given to The chemical parameters EPA. include major cations and an- ions and heavy metals. These include Si02 , ca, Mg, Na, K, Ground water Mn, F-, B, Br, c1-, Fe total, Fe2+, Fe3 +, NOH, so4+, and s 2-. on-site Monitoring Well.one Heavy metals include Cd, er•+, sample was taken from an on- Co, Cu, Pb, Hg, Mo, Ni, Ag, and site monitoring well (Figure Zn. 3). A one-liter teflon bailer was used to obtain the sample. Certain cations/anions 2 4 Before sampling, three volumes such as Fe, s -, and so + are of well casing water was purged very sensitive to changes of Eh using the bailer. One split (redox) with respect to time. was given to EPA. Therefore, filtering using tra- ditional aeration methods (vac- uum or pressure) was not pre- Location control ferred or performed. The underwater springs Ratios by weight were also release both hydrothermal flu- calculated. These include Br/- ids and gas. The telltale bub- Cl, K/Na, and B/Cl. These ra- bles on the surface from the tios are useful in determining generated gas are an indicator the water's commonality. of the spring's general loca- tion on the bottom - especially since there are virtually no Near-site Laboratory currents within the Herman Pit and Clear Lake. A 14-foot in- An analytical laboratory flatable boat was used as an was setup by the U.S. Bureau of operating platform. Its compo- Mines in the town of Clear sition is hypalon and neoprene Lake, about one mile from the which are resistant to acidic Sulphur Bank Mine site. Water waters such as found in Herman samples were taken from the Pit. site and analyzed using wet chemistry methods. Analytical instruments included a labora- Sample Analyses tory spectrophotometer, pH/Eh meter (with Na and K probes), Phvsical and Chemical Parame- specific conductivity meter, ters. A suite of physical and 170 --~-- ------- and a dissolved oxygen meter. on August 28, 1992 from Clear Lake, California to Las Vegas, Half (13 of 26) of the Nevada via Federal Express one- analytical methods performed at day service. USEPA's analyses the near-site laboratory are were performed on September 17, USEPA approved for reporting 1992. purposes. These include Mn, F- Fe total Fe2+ Fes+ NOH I 2 6I I I I so•+ I s -I cr +I cu I Pb I Ni· I and Quality Control Zn. Sampling Technique Cations and anions such as Fe total, Fe2+, Fe3+, c1-, soH, Standard USEPA water sam- 2 s -, and metals were analyzed pling protocol was observed immediately. The remaining during all sampling events. cations and anions were refrig- Splits were formed by filling erated and analyzed within 24 an equal portion in each bottle hours of sampling. then reversing the procedure until each bottle was full. The mercury analytical Headspace was minimized for all procedure used is a newly de- samples.