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James J. Rytuba

Publications and source records attributed to James J. Rytuba.

At least 19 recordsLinked to original sources

Geology and mineral resources of the Sheldon-Hart Mountain National Wildlife Refuge Complex (Oregon and Nevada), the Southeastern Oregon and North-Central Nevada, and the Southern Idaho and Northern Nevada (and Utah) Sagebrush Focal Areas: Chapter B in Mineral resources of the Sagebrush Focal Areas of Idaho, Montana, Nevada, Oregon, Utah, and Wyoming

Summary The U.S. Department of the Interior has proposed to withdraw approximately 10 million acres of Federal lands from mineral entry (subject to valid existing rights) from 12 million acres of lands defined as Sagebrush Focal Areas (SFAs) in Idaho, Montana, Nevada, Oregon, Utah, and Wyoming (for further discussion on the lands involved see Scientific Investigations Report 2016–5089–A). The purpose of the proposed action is to protect the greater sage-grouse ( Centrocercus urophasianus ) and its habitat from potential adverse effects of locatable mineral exploration and mining. The U.S. Geological Survey Sagebrush Mineral-Resource Assessment (SaMiRA) project was initiated in November 2015 and supported by the Bureau of Land Management to (1) assess locatable mineral-resource potential and (2) to describe leasable and salable mineral resources for the seven SFAs and Nevada additions. This chapter summarizes the current status of locatable, leasable, and salable mineral commodities and assesses the potential of selected locatable minerals in lands proposed for withdrawal that span the Nevada, Oregon, Idaho, and Utah borders. In this report, the four study areas evaluated were (1) the Sheldon-Hart Mountain National Wildlife Refuge Complex SFA in Washoe County, Nevada, and Harney and Lake Counties, Oregon; (2) the Southeastern Oregon and North-Central Nevada SFA in Humboldt County, Nevada, and Harney and Malheur Counties, Oregon; (3) the Southern Idaho and Northern Nevada SFA in Cassia, Owyhee, and Twin Falls Counties, Idaho, Elko County, Nevada, and Box Elder County, Utah; and (4) the Nevada additions in Humboldt and Elko Counties, Nevada.

Idaho, Nevada, Oregon, Utah

Environmental assessment of water, sediment, and biota collected from the Bear Creek watershed, Colusa County, California

The Cache Creek watershed lies within California's North Coast Range, an area with abundant geologic sources of mercury (Hg) and a long history of Hg contamination (Rytuba, 2000). Bear Creek, Cache Creek, and the North Fork of Cache Creek are the major streams of the Cache Creek watershed, encompassing 2978 km 2 . The Cache Creek watershed contains soils naturally enriched in Hg as well as natural springs (both hot and cold) with varying levels of aqueous Hg (Domagalski and others, 2004, Suchanek and others, 2004, Holloway and others 2009). All three tributaries are known to be significant sources of anthropogenically derived Hg from historic mines, both Hg and gold (Au), and associated ore storage/processing sites and facilities (Slotton and others, 1995, 2004; CVRWQCB, 2003; Schwarzbach and others, 2001; Gassel and others, 2005; Suchanek and others., 2004, 2008a, 2009). Historically, two of the primary sources of mercury contamination in the upper part of Bear Creek have been the Rathburn and Petray Hg Mines. The Rathburn Hg mine was discovered and initially mined in the early 1890s. The Rathburn and the more recently developed Petray open pit mines are localized along fault zones in serpentinite that has been altered and cut by quartz and chalcedony veins. Cold saline-carbonate springs are located perepheral to the Hg deposits and effluent from the springs locally has high concentrations of Hg (Slowey and Rytuba, 2008). Several ephemeral tributaries to Bear Creek drain the mine area which is located on federal land managed by the U.S. Bureau of Land Management (USBLM). The USBLM requested that the U.S. Geological Survey (USGS) measure and characterize Hg and other geochemical constituents in sediment, water, and biota to establish baseline information prior to remediation of the Rathburn and Petray mines. Samples sites were established in Bear Creek upstream and downstream from the mine area. This report is made in response to the USBLM request, the lead agency mandated to conduct a Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) - Removal Site Investigation (RSI). The RSI applies to the possible removal of Hg-contaminated mine waste from Bear Creek. This report summarizes data obtained from field sampling of water, sediment, and biota in Bear Creek, above input from the mine area and downstream from the Rathburn-Petray mine area to the confluence with Cache Creek. Our results permit a preliminary assessment of the chemical constituents that could elevate levels of monomethyl Hg (MMeHg) in Bear Creek and its uptake by biota and provide baseline information for comparison to conditions after mine remediation is completed.

California

Geologic map of the Bodie Hills, California and Nevada

The Bodie Hills covers about 1,200 km 2 straddling the California-Nevada state boundary just north of Mono Lake in the western part of the Basin and Range Province, about 20 km east of the central Sierra Nevada. The area is mostly underlain by the partly overlapping, middle to late Miocene Bodie Hills volcanic field and Pliocene to late Pleistocene Aurora volcanic field (John and others, 2012). Upper Miocene to Pliocene sedimentary deposits, mostly basin-filling sediments, gravel deposits, and fanglomerates, lap onto the west, north, and east sides of the Bodie Hills, where they cover older Miocene volcanic rocks. Quaternary surficial deposits, including extensive colluvial, fluvial, glacial, and lacustrine deposits, locally cover all older rocks. Miocene and younger rocks are tilted ≤30° in variable directions. These rocks are cut by several sets of high-angle faults that exhibit a temporal change from conjugate northeast-striking left-lateral and north-striking right-lateral oblique-slip faults in rocks older than about 9 Ma to north- and northwest-striking dip-slip faults in late Miocene rocks. The youngest faults are north-striking normal and northeast-striking left-lateral oblique-slip faults that cut Pliocene-Pleistocene rocks. Numerous hydrothermal systems were active during Miocene magmatism and formed extensive zones of hydrothermally altered rocks and several large mineral deposits, including gold- and silver-rich veins in the Bodie and Aurora mining districts (Vikre and others, in press).

California, Nevada

Assessment of mercury and methylmercury in water, sediment, and biota in Sulphur Creek in the vicinity of the Clyde Gold Mine and the Elgin Mercury Mine, Colusa County, California

At the request of the U.S. Bureau of Land Management, we performed a study during April–July 2010 to characterize mercury (Hg), monomethyl mercury (MMeHg), and other geochemical constituents in sediment, water, and biota at the Clyde Gold Mine and the Elgin Mercury Mine, located in neighboring subwatersheds of Sulphur Creek, Colusa County, California. This study was in support of a Comprehensive Environmental Response, Compensation, and Liability Act - Removal Site Investigation. The investigation was in response to an abatement notification from the California Central Valley Regional Water Quality Control Board to evaluate the release of Hg from the Clyde and Elgin mines. Samples of water, sediment, and biota (aquatic macroinvertebrates) were collected from sites upstream and downstream from the two mine sites to evaluate the level of Hg contamination contributed by each mine to the aquatic ecosystem. Physical parameters, as well as dissolved organic carbon, total Hg (Hg T ), and MMeHg were analyzed in water and sediment. Other relevant geochemical constituents were analyzed in sediment, filtered water, and unfiltered water. Samples of aquatic macroinvertebrates from each mine were analyzed for Hg T and MMeHg. The presence of low to moderate concentrations of Hg T and MMeHg in water, sediment, and biota from the Freshwater Branch of Sulphur Creek, and the lack of significant increases in these concentrations downstream from the Clyde Mine indicated that this mine is not a significant source of Hg to the watershed during low flow conditions. Although concentrations of Hg T and MMeHg were generally higher in samples of sediment and water from the Elgin Mine compared to the Clyde Mine, concentrations in comparable biota from the two mine areas were similar. It is likely that highly saline effluent from nearby hot springs contribute more Hg to the West Fork of Sulphur Creek than the mine waste material at the Elgin Mine.

California

Fluvial transport and surface enrichment of arsenic in semi-arid mining regions: examples from the Mojave Desert, California

As a result of extensive gold and silver mining in the Mojave Desert, southern California, mine wastes and tailings containing highly elevated arsenic (As) concentrations remain exposed at a number of former mining sites. Decades of weathering and erosion have contributed to the mobilization of As-enriched tailings, which now contaminate surrounding communities. Fluvial transport plays an intermittent yet important and relatively undocumented role in the migration and dispersal of As-contaminated mine wastes in semi-arid climates. Assessing the contribution of fluvial systems to tailings mobilization is critical in order to assess the distribution and long-term exposure potential of tailings in a mining-impacted environment. Extensive sampling, chemical analysis, and geospatial mapping of dry streambed (wash) sediments, tailings piles, alluvial fans, and rainwater runoff at multiple mine sites have aided the development of a conceptual model to explain the fluvial migration of mine wastes in semi-arid climates. Intense and episodic precipitation events mobilize mine wastes downstream and downslope as a series of discrete pulses, causing dispersion both down and lateral to washes with exponential decay behavior as distance from the source increases. Accordingly a quantitative model of arsenic concentrations in wash sediments, represented as a series of overlapping exponential power-law decay curves, results in the acceptable reproducibility of observed arsenic concentration patterns. Such a model can be transferable to other abandoned mine lands as a predictive tool for monitoring the fate and transport of arsenic and related contaminants in similar settings. Effective remediation of contaminated mine wastes in a semi-arid environment requires addressing concurrent changes in the amounts of potential tailings released through fluvial processes and the transport capacity of a wash.

California

Geology and geochemistry of volcanic centers within the eastern half of the Sonoma volcanic field, northern San Francisco Bay region, California

Volcanic rocks in the Sonoma volcanic field in the northern California Coast Ranges contain heterogeneous assemblages of a variety of compositionally diverse volcanic rocks. We have used field mapping, new and existing age determinations, and 343 new major and trace element analyses of whole-rock samples from lavas and tuff to define for the first time volcanic source areas for many parts of the Sonoma volcanic field. Geophysical data and models have helped to define the thickness of the volcanic pile and the location of caldera structures. Volcanic rocks of the Sonoma volcanic field show a broad range in eruptive style that is spatially variable and specific to an individual eruptive center. Major, minor, and trace-element geochemical data for intracaldera and outflow tuffs and their distal fall equivalents suggest caldera-related sources for the Pinole and Lawlor Tuffs in southern Napa Valley and for the tuff of Franz Valley in northern Napa Valley. Stratigraphic correlations based on similarity in eruptive sequence and style coupled with geochemical data allow an estimate of 30 km of right-lateral offset across the West Napa-Carneros fault zones since ∼5 Ma. The volcanic fields in the California Coast Ranges north of San Francisco Bay are temporally and spatially associated with the northward migration of the Mendocino triple junction and the transition from subduction and associated arc volcanism to a slab window tectonic environment. Our geochemical analyses from the Sonoma volcanic field highlight the geochemical diversity of these volcanic rocks, allowing us to clearly distinguish these volcanic rocks from those of the roughly coeval ancestral Cascades magmatic arc to the west, and also to compare rocks of the Sonoma volcanic field to rocks from other slab window settings.

California

Review of samples of sediments, tailings, and waters adjacent to the Cactus Queen Gold Mine, Kern County, California

The Cactus Queen Mine is located in the western Mojave Desert in Kern County, California. The Cactus Queen gold-silver (Au-Ag) deposit is similar to other Au-Ag deposits hosted in Miocene volcanic rocks that consist of silicic domes and associated flows, pyroclastic rocks, and subvolcanic intrusions. The volcanic rocks were emplaced onto a basement of Mesozoic silicic intrusive rocks. A part of the Cactus Queen Mine is located on Federal land managed by the U.S. Bureau of Land Management (BLM). Staff from the BLM initially sampled the mine area and documented elevated concentrations of arsenic (As) in tailings and sediment. BLM then requested that the U.S. Geological Survey (USGS), in collaboration with Chapman University, measure and characterize As and other geochemical constituents in sediment, tailings, and waters on the part of the mine on Federal lands. This report is made in response to the request by the BLM, the lead agency mandated to conduct a Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) - Removal Site Investigation (RSI). The RSI applies to the potential removal of As-contaminated mine waste from the Cactus Queen Mine as a means of reducing As release and exposure to humans and biota. This report summarizes data obtained from field sampling of sediments, mine tailings, and surface waters at the Cactus Queen Mine on January 27, 2008. Our results provide a preliminary assessment of the sources of As and associated chemical constituents that could potentially impact humans and biota.

California

Review of samples of tailings, soils, and stream sediments adjacent to and downstream from the Ruth Mine, Inyo County, California

The Ruth Mine and mill are located in the western Mojave Desert in Inyo County, California (fig. 1). The mill processed gold-silver (Au-Ag) ores mined from the Ruth Au-Ag deposit, which is adjacent to the mill site. The Ruth Au-Ag deposit is hosted in Mesozoic intrusive rocks and is similar to other Au-Ag deposits in the western Mojave Desert that are associated with Miocene volcanic centers that formed on a basement of Mesozoic granitic rocks (Bateman, 1907; Gardner, 1954; Rytuba, 1996). The volcanic rocks consist of silicic domes and associated flows, pyroclastic rocks, and subvolcanic intrusions (fig. 2) that were emplaced into Mesozoic silicic intrusive rocks (Troxel and Morton, 1962). The Ruth Mine is on Federal land managed by the U.S. Bureau of Land Management (BLM). Tailings from the mine have been eroded and transported downstream into Homewood Canyon and then into Searles Valley (figs. 3, 4, 5, and 6). The BLM provided recreational facilities at the mine site for day-use hikers and restored and maintained the original mine buildings in collaboration with local citizen groups for use by visitors (fig. 7). The BLM requested that the U.S. Geological Survey (USGS), in collaboration with Chapman University, measure arsenic (As) and other geochemical constituents in soils and tailings at the mine site and in stream sediments downstream from the mine in Homewood Canyon and in Searles Valley (fig. 3). The request was made because initial sampling of the site by BLM staff indicated high concentrations of As in tailings and soils adjacent to the Ruth Mine. This report summarizes data obtained from field sampling of mine tailings and soils adjacent to the Ruth Mine and stream sediments downstream from the mine on June 7, 2009. Our results permit a preliminary assessment of the sources of As and associated chemical constituents that could potentially impact humans and biota.

California

Review of samples of water, sediment, tailings, and biota at the Little Bonanza mercury mine, San Luis Obispo County, California

Background and Objectives The Little Bonanza mercury (Hg) mine, located in San Luis Obispo County, California, is a relatively small mine with, a historical total Hg production of about 1,000 flasks. The mine workings and tailings are located in the headwaters of the previously unnamed west fork of Las Tablas Creek (WF Las Tablas Creek), which flows into the Nacimiento Reservoir. Wasterock and tailings eroded from the Little Bonanza Hg Mine have contributed Hg-enriched mine wastes to the headwaters of WF Las Tablas Creek. The mine is located on Federal land managed by the U.S. Bureau of Land Management (BLM), which requested that the U.S. Geological Survey (USGS) measure and characterize Hg and other geochemical constituents in tailings, sediment, water, and biota at and downstream from the minesite. This report is in response that request, from the lead agency which is mandated to conduct a Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) - Removal Site Investigation (RSI). The RSI applies to removal of Hg-contaminated mine waste from the Little Bonanza minesite as a means of reducing Hg transport to WF Las Tablas Creek. This report summarizes data obtained from field sampling of mine tailings, wasterock, sediment, water, and biota at the Little Bonanza Mine that was completed on April 6, 2010. Conditions during sampling were dry and no rain had occurred in the watershed for several weeks. Our results permit a preliminary assessment of the mining sources of Hg and associated chemical constituents that could produce elevated levels of monomethyl mercury (MMeHg) in WF Las Tablas Creek and in biota. History and Geology The history of the Little Bonanza Hg mine is summarized here from Yates (1943) and other references as cited. The Little Bonanza Mine, located 20 mi west of Paso Robles, was discovered in 1862. Although production was minor until 1900, from 1900 to 1906, the mine produced about 1,000 flasks of Hg. Intermittent production continued into the 1940s but was relatively limited. Underground workings, now caved and inaccessible, include about 3,000 ft of drifts, crosscuts, and raises on three levels extending 260 ft downward. The workings at the Little Bonanza Mine explore a zone of fault breccia, which trends northwest. The breccia is composed of fragments of sandstone, greenstone, serpentine, and chert in a shale matrix. The serpentine has been hydrothermally altered to silica-carbonate rock, and the Hg deposit is hosted within the zone of alteration. The veins are discontinuous and irregular, but form a steplike pattern along the fault zone. The principal mineralization occurring in the veins is irregular, consisting of disseminated zones of cinnabar. Most of the veins in the mine area contain cinnabar. Sample Sites and Methods Samples were collected to assess the concentrations of Hg and biogeochemically relevant constituents in tailings and wasterock piles at the Little Bonanza Hg mine. Tailings are present adjacent to a three-pipe retort used to process the Hg ore. The tailings occur in the upper 15 cm of the soil adjacent to the retort and slag from the retort is present on the surface. An area of disturbed soil and rock uphill from the retort was likely formed during construction of a dam that provided water for mining activities. Wasterock in these piles was sampled. The largest amount of tailings is exposed to the west of the retort in the bank of WF Las Tablas Creek. Water, sediment, and biota were sampled from WF Las Tablas Creek, which flows through the mine area. Sample-site locations are shown in figures 10 and 11 and listed in table 1. Samples were collected when streamflow was low and no precipitation had occurred.

California

Impact of mine and natural sources of mercury on water, sediment, and biota in Harley Gulch adjacent to the Abbott-Turkey Run mine, Lake County, California

Executive Summary Stable-isotope data indicate that there are three sources of water that effect the composition and Hg concentration of waters in Harley Gulch: (1) meteoric water that dominates water chemistry during the wet season; (2) thermal water effluent from the Turkey Run mine that effects the chemistry at sample site HG1; and (3) cold connate groundwater that dominates water chemistry during the dry season as it upwells and reaches the surface. The results from sampling executed for this study suggest four distinct areas in Harley Gulch: (1) the contaminated West Fork of Harley Gulch, consisting of the stream immediately downstream from the mine area and the wetlands upstream from Harley Gulch canyon (sample sites HG1-HG2, (2) the East Fork of Harley Gulch, where no mining has occurred (sample site HG3), (3) sample sites HG4-HG7, where a seasonal influx of saline groundwater alters stream chemistry, and (4) sample sites HG7-HG10, downstream in Harley Gulch towards the confluence with Cache Creek. West Fork: Mine Area and Wetlands The concentration of Hg in both storm sediment and active channel sediment was highest at sample site HG1, immediately downstream from the mine. The highest concentrations of total Hg (Hg T ) in water also occurred at site HG1, and they decreased systematically downstream from the mine. The high concentration of HgT at site HG1 reflects input of thermal-water effluent from the Turkey Run mine which comprises most of the flow at this site during the dry season. During the May 2011 low-flow sampling, Hg T concentration was very high at site HG1, but the maximum in HgT concentration occurred at sample site HG1.5 in the middle of the wetland area. The high concentration of Hg T and isotopic chemistry at this site indicates that a significant input of connate groundwater into the creek at this location contributes to the high Hg concentration in water. At site HG1, just downstream from the thermal water input from the Turkey Run mine, water sampled in June 2010 was almost entirely composed of thermal-water effluent. During the storm sampling in March 2011, which resulted in the highest flows of the winter, thermal effluent was virtually undetectable at site HG1, and the water was all meteoric. During the May 2011 sampling event, the input of connate groundwater in the middle of the wetland area at site HG1.5 was dominant. Discharge from the adit and runoff from the mine contributes to the high Hg concentration at site HG1 under both high and low-flow conditions. East Fork: Background Hg levels in waters collected from the East Fork of Harley Gulch, where no mining has occurred, were as high as 32.8 parts per trillion (pptr). These levels of Hg in water are significantly higher than regional background Hg concentrations, which range from 4-7 pptr. These anomalous Hg concentrations are partially explained by the abundance of Hg-enriched groundwater in Harley Gulch. Sites HG4-HG7 Downstream from the wetland, the aqueous concentration of HgT decreased, but remained above background levels as another input of connate groundwater occurs in the creek segment between sample sites HG4 and HG7. The input of connate groundwater in this segment of the creek is reflected in the increase in dissolved constituents characteristic of the connate groundwater, such as sulfate (SO4), chloride (Cl) and magnesium (Mg). Stable-isotope data for heavy isotopes d18O and d2D also confirm two areas of input of connate groundwater into Harley Gulch: the creek segment in the West Fork near sample site HG1.5 and the segment between sample sites HG4 and HG7. Downstream from the second area of input of connate groundwater, both HgF and Hg T concentrations decrease similarly, but the percentage of Hg in the filtered fraction increases. The decreases in HgT and HgF between sample sites HG5 and HG7 suggests that this second source of connate groundwater to Harley Gulch is distinct from the Hg-enriched source that enters the middle of the wetlands at sample site HG1.5. During low-flow conditions in June 2010, input of connate groundwater increased from sample site HG4 and reached a maximum near sample site HG7, where it dominated creek water chemistry. Waters collected from sample site HG7 during the June 2010 sampling event were the heaviest isotopically and contained high concentrations of Cl and SO4, constituents that are characteristically high in the connate groundwater. Both above and below sample site HG7, the amount of connate groundwater in the creek water decreased. Sites HG8-HG10 Sediment with high Hg concentration is present throughout the West Fork of Harley Gulch below the mine and in the upper part of the Harley Gulch main stem to just above sample site HG10. At the sample site furthest downstream, HG10, Hg concentration is at background levels, as are cobalt (Co), nickel (Ni), and tungsten (W), indicating that the sediment is not significantly contaminated with Hg from the mine.

California

Mercury assessment and monitoring protocol for the Bear Creek Watershed, Colusa County, California

This report summarizes the known information on the occurrence and distribution of mercury (Hg) in physical/chemical and biological matrices within the Bear Creek watershed. Based on these data, a matrix-specific monitoring protocol for the evaluation of the effectiveness of activities designed to remediate Hg contamination in the Bear Creek watershed is presented. The monitoring protocol documents procedures for collecting and processing water, sediment, and biota for estimation of total Hg (TotHg) and monomethyl mercury (MMeHg) in the Bear Creek watershed. The concurrent sampling of TotHg and MMeHg in biota as well as water and sediment from 10 monitoring sites is designed to assess the relative bioavailability of Hg released from Hg sources in the watershed and identify environments conducive to Hg methylation. These protocols are designed to assist landowners, land managers, water quality regulators, and scientists in determining whether specific restoration/mitigation actions lead to significant progress toward achieving water quality goals to reduce Hg in Bear and Sulphur Creeks.

California

Environmental Impact of the Contact and Sonoma Mercury Mines on Water, Sediment, and Biota in Anna Belcher and Little Sulphur Creek Watersheds, Sonoma County, California

The Contact and Sonoma mercury (Hg) deposits are among the youngest Hg deposits in the Coast Range Hg mineral belt and are located in the western part of the Clear Lake volcanic field in Sonoma County, California. The mine workings and tailings are located in the headwaters of Anna Belcher Creek, which is a tributary to Little Sulphur Creek. The Contact Hg mine produced about 1,000 flasks of Hg, and the Sonoma mine produced considerably less. Waste rock and tailings eroded from the Contact and Sonoma mines have contributed Hg-enriched mine waste material to the headwaters of Anna Belcher Creek. The mines are located on federal land managed by the U.S. Bureau of Land Management (USBLM). The USBLM requested that the U.S. Geological Survey (USGS) measure and characterize Hg and other geochemical constituents in tailings, sediment, water, and biota at the Contact and Sonoma mines and in Anna Belcher and Little Sulphur Creeks. This report is made in response to the USBLM request, the lead agency mandated to conduct a Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) - Removal Site Investigation (RSI). The RSI applies to removal of Hg-contaminated mine waste from the Contact and Sonoma mines as a means of reducing Hg transport to Anna Belcher and Little Sulphur Creeks. This report summarizes data obtained from field sampling of mine tailings, waste rock, sediment, and water at the Contact and Sonoma mines that was initiated on April 20 during a storm event, and on June 19, 2001. Further sampling of water, sediment, and biota in a pond and tributaries that drain from the mine area was completed on April 1, 2003. Our results permit a preliminary assessment of the mining sources of Hg and associated chemical constituents that could elevate levels of monomethyl Hg (MMeHg) in tributaries and biota that are impacted by historic mining.

Open-File Report

Environmental Impact of the Helen, Research, and Chicago Mercury Mines on Water, Sediment, and Biota in the Upper Dry Creek Watershed, Lake County, California

The Helen, Research, and Chicago mercury (Hg) deposits are among the youngest Hg deposits in the Coast Range Hg mineral belt and are located in the southwestern part of the Clear Lake volcanic field in Lake County, California. The mine workings and tailings are located in the headwaters of Dry Creek. The Helen Hg mine is the largest mine in the watershed having produced about 7,600 flasks of Hg. The Chicago and Research Hg mines produced only a small amount of Hg, less than 30 flasks. Waste rock and tailings have eroded from the mines, and mine drainage from the Helen and Research mines contributes Hg-enriched mine wastes to the headwaters of Dry Creek and contaminate the creek further downstream. The mines are located on federal land managed by the U.S. Bureau of Land Management (USBLM). The USBLM requested that the U.S. Geological Survey (USGS) measure and characterize Hg and geochemical constituents in tailings, sediment, water, and biota at the Helen, Research, and Chicago mines and in Dry Creek. This report is made in response to the USBLM request to conduct a Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA - Removal Site Investigation (RSI). The RSI applies to removal of Hg-contaminated mine waste from the Helen, Research, and Chicago mines as a means of reducing Hg transport to Dry Creek. This report summarizes data obtained from field sampling of mine tailings, waste rock, sediment, and water at the Helen, Research, and Chicago mines on April 19, 2001, during a storm event. Further sampling of water, sediment, and biota at the Helen mine area and the upper part of Dry Creek was completed on July 15, 2003, during low-flow conditions. Our results permit a preliminary assessment of the mining sources of Hg and associated chemical constituents that could elevate levels of monomethyl Hg (MMeHg) in the water, sediment, and biota that are impacted by historic mining.

Open-File Report

Mercury geochemistry of gold placer tailings, sediments, bedrock, and waters in the lower Clear Creek area, Shasta County, California— Report of investigations, 2001-2003

Clear Creek, one of the major tributaries of the upper Sacramento River, drains the eastern Trinity Mountains. Alluvial plain and terrace gravels of lower Clear Creek, at the northwest edge of the Sacramento Valley, contain placer gold that has been mined since the Gold Rush by various methods including hydraulic mining and dredging. In addition, from the 1950s to the 1980s aggregate-mining operations removed gravel from the lower Clear Creek flood plain. Since Clear Creek is an important stream for salmon production, a habitat restoration program is underway to repair damage from mining and improve conditions for spawning. This program includes moving dredge tailings to increase the area of spawning gravel and to fill gravel pits in the flood plain, raising the concern that mercury lost to these tailings in the gold recovery process may be released and become available to biota. The purposes of our study are to identify sources, transport, and dispersal of mercury in the lower Clear Creek area and identify environments in which bioavailable methylmercury is produced. Analytical data acquired include total mercury and methylmercury concentrations in sediments, tailings, and water. Mercury concentrations in bedrock and unmined gravels in and around the mined area are low and are taken to represent background concentrations. Bulk mercury values in placer mining tailings range from near-background in coarse dry materials to more than 40 times background in sands and silts exposed to mercury in sluices. Tailings are entrained in flood-plain sediments and active stream sediments; consequently, mercury concentrations in these materials range from background to about two to three times background. Mercury in sediments and tailings is associated with fine size fractions. The source of most of this mercury is historical gold mining in the Clear Creek watershed. Although methylmercury levels are low in most of these tailings and sediments, flood-plain sediment in shallow flood-plain ponds, tailings in a dredge pond, and active stream sediment in a Clear Creek backwater have elevated levels of methylmercury. Stream waters in the area show low mercury levels during both summer and winter base-flow conditions. During winter high flows total mercury increases by about one order of magnitude; this additional mercury is associated with suspended particulate material. Methylmercury is low in stream waters. Ponds in various environments generally have higher total mercury levels in waters than Clear Creek under base-flow conditions and higher methylmercury levels in both sediments and waters. Ponds are probably the main source of bioavailable mercury in the lower Clear Creek area. Several saline springs occur in the area. The saline waters are enriched in lithium, boron, and mercury, similar to connate waters that are expelled along thrust faults to the south on the west side of the Sacramento Valley. Saline springs may locally contribute some mercury to pond and drainage waters.

California

Mercury Release from the Rathburn Mine, Petray Mine, and Bear Valley Saline Springs, Colusa County, California 2004-2006

This report summarizes data obtained from field sampling of mine tailings and waste rock at the Rathburn and Petray Mines that was initiated in July 17, 2001 and water and sediment in regional springs and tributaries that drain from the mine area into Bear Creek on December 14, 2004 and February 16 and May 27, 2005. Although it was initially assumed that the mines were the cause of elevated levels of monomethyl Hg measured by the Central Regional Water Quality Control Board in tributaries near their confluence with Bear Creek (Foe and others, unpublished results), it became apparent during this study that ground water springs were also potential sources of Hg. In addition to sampling of springs in May 2005, saline ground water seepage along an unnamed fault on the west side of Bear Valley was sampled on December 13-14, 2006. We did not sample water or sediment in Bear Creek itself during this study. Our results permit a preliminary assessment of mining and natural sources of Hg and associated chemical constituents that could elevate levels of monomethyl Hg in Bear Creek.

Open-File Report

Understanding Metal Pathways in Mineralized Ecosystems

Successful management of ecosystems containing historical mine wastes requires understanding of processes that are responsible for the distribution, concentration, and bioavailability of potentially toxic elements. U.S. Geological Survey (USGS) scientists recently completed several investigations at historical mine sites in the western United States. These investigations have improved our understanding of how metals are mobilized from mineralized sources, are transported through the environment, and become available to humans and other biota. The new information is being used by Federal, State, and local agencies that manage and remediate abandoned mine lands.

Circular

Mercury at the Oat Hill Extension Mine and James Creek, Napa County, California: Tailings, sediment, water, and biota, 2003-2004

The Oat Hill Extension (OHE) Mine is one of several mercury mines located in the James Creek/Pope Creek watershed that produced mercury from the 1870's until 1944 (U.S. Bureau of Mines, 1965). The OHE Mine developed veins and mineralized fault zones hosted in sandstone that extended eastward from the Oat Hill Mine. Waste material from the Oat Hill Mine was reprocessed at the OHE Mine using gravity separation methods to obtain cinnabar concentrates that were processed in a retort. The U.S. Bureau of Land Management requested that the U.S. Geological Survey measure and characterize mercury and other chemical constituents that are potentially relevant to ecological impairment of biota in tailings, sediment, and water at the OHE Mine and in the tributaries of James Creek that drain the mine area (termed Drainage A and B ) (Figs. 1 and 2). This report summarizes such data obtained from sampling of tailings and sediments at the OHE on October 17, 2003; water, sediment, and biota from James Creek on May 20, 2004; and biota on October 29, 2004. These data are interpreted to provide a preliminary assessment of the potential ecological impact of the mine on the James Creek watershed. The mine tailings are unusual in that they have not been roasted and contain relatively high concentrations of mercury (400 to 1200 ppm) compared to unroasted waste rock at other mines. These tailings have contaminated a tributary to James Creek with mercury primarily by erosion, on the basis of higher concentration of mercury (780 ng/L) measured in unfiltered (total mercury, Hg T ) spring water flowing from the OHE to James Creek compared to 5 to 14 ng/L Hg T measured in James Creek itself. Tailing piles (presumably from past Oat Hill mine dumping) near the USBLM property boundary and upstream of the main OHE mine drainage channel ( Drainage A ; Fig. 2) also likely emit mercury, on the basis of their mercury composition (930 to 1200 ppm). The OHE spring water is likely an appreciable source of sulfate and carbonate to James Creek, because the spring water was enriched in sulfate (130 mg/L) and carbonate (430 mg/L as CaCO 3 ) compared to James Creek water (70 to 100 mg/L SO 4 2- and 110 to 170 mg/L as CaCO 3 ) at the time of sampling. Concentrations of mercury in active channel sediment from James Creek are variable and potentially high, on the basis of chemical analysis (2.5 to 17 _g/g-wet sediment) and easily visible cinnabar grains in panned concentrates. Average (geometric mean) organic mercury (presumably monomethyl mercury (MMHg); §2.3.3) concentrations in several invertebrate taxa collected from the James Creek watershed locations were higher than invertebrates taken from a Northern California location lacking a known point source of mercury. The mean proportion of MMHg to total mercury in James Creek predatory insect samples was 40 percent (1 standard deviation = 30 percent); only 40 percent of all insect samples had a MMHg/Hg T proportion greater than 0.5. The low proportions of MMHg measured in invertebrates in James Creek and the presence of cinnabar in the creek suggest that some invertebrates may have anomolously high Hg concentrations as a result of the injestion or adhesion of extremely fine-grained cinnabar particles. Interpretation of Hg T in frogs and fish as an indicator of mercury reactivity, biouptake, or trophic transfer is limited, pending MMHg measuremens, by the possibility of these whole-body samples having contained cinnabar particles at the time of analysis. To minimize this limitation, the gastrointestinal tracts and external surfaces of all amphibians, where cinnabar most likely resides, were carefully flushed to remove any visible particles. However, extremely fine-grained, invisible, adhesive cinnabar particles likely exist in the amphibians' habitats. Hg T in foothill yellow-legged frogs collected from the James Creek study area, ranging from 0.1 to 0.6 μg/g Hg, was on average twice that of an extensive database compiled from Hg T in frogs studied throughout Northern California. Average concentrations of Hg T in frogs from James Creek were similar upstream (0.18 μg/g) and downstream (0.15 μg/g) of the confluence with Tributary 1 and at the lower Corona Mine adit drainage (0.14 μg/g). Frogs may be susceptible to trophic transfer of MMHg from invertebrates, but further study is required to rule out cinnabar ‘contamination.’ Hg T concentrations in rainbow trout collected from James Creek upstream and downstream of Tributary 1 averaged 0.10 μg/g and 0.13 μg/g, respectively. Compared to invertebrates, trout Hg T was less variable, suggesting that trout were less contaminated with cinnabar. California roach had significantly higher Hg T on average than trout (0.16 vs. 0.12 μg/g), and can be considered moderately contaminated compared to the same species from other sites in Northern California, which average 0.12 μg/g Hg. While limited measurements of mercury in water, sediment, and fish exceed, in some samples, predefined ecologically protective criteria for mine-impacted California systems, they do not clearly demonstrate that the biota residing in James Creek in the vicinity of the OHE are ecologically impaired. The potential for ecological impairment is clearly evident from invertebrate methyl mercury results and may manifest in other biological ecosystem residents that have yet to be studied (e.g., piscivorous birds). Methyl mercury concentrations in flowing water and sediment from James Creek and the tributary that drains the OHE are relatively low, ranging from 0.04 to 0.08 ng/L, although these data should be cautiously interpreted (see §3.2). While the results of this investigation suggest that the OHE contributes inorganic mercury to James Creek, they do not indicate the extent to which the OHE site is ecologically impairing biota relative to other sources of mercury. Improved sampling and analytical methods are recommended for future study.

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