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Geology topics

K. S. Smith

Publications and source records attributed to K. S. Smith.

At least 19 recordsLinked to original sources

Approach for environmental baseline water sampling

Samples collected during the exploration phase of mining represent baseline conditions at the site. As such, they can be very important in forecasting potential environmental impacts should mining proceed, and can become measurements against which future changes are compared. Constituents in stream water draining mined and mineralized areas tend to be geochemically, spatially, and temporally variable, which presents challenges in collecting both exploration and baseline water-quality samples. Because short-term (daily) variations can complicate long-term trends, it is important to consider recent findings concerning geochemical variability of stream-water constituents at short-term timescales in designing sampling plans. Also, adequate water-quality information is key to forecasting potential ecological impacts from mining. Therefore, it is useful to collect baseline water samples adequate tor geochemical and toxicological modeling. This requires complete chemical analyses of dissolved constituents that include major and minor chemical elements as well as physicochemical properties (including pH, specific conductance, dissolved oxygen) and dissolved organic carbon. Applying chemical-equilibrium and appropriate toxicological models to water-quality information leads to an understanding of the speciation, transport, sequestration, bioavailability, and aquatic toxicity of potential contaminants. Insights gained from geochemical and toxicological modeling of water-quality data can be used to design appropriate mitigation and for economic planning for future mining activities.

Conference Paper

An enriched stable-isotope approach to determine the gill-zinc binding properties of juvenile rainbow trout (Oncorhynchus mykiss) during acute zinc exposures in hard and soft waters

The objective of the present study was to employ an enriched stable-isotope approach to characterize Zn uptake in the gills of rainbow trout (Oncorhynchus mykiss) during acute Zn exposures in hard water (???140 mg/L as CaCO 3 ) and soft water (???30 mg/L as CaCO 3 ). Juvenile rainbow trout were acclimated to the test hardnesses and then exposed for up to 72 h in static exposures to a range of Zn concentrations in hard water (0-1,000 ??g/L) and soft water (0-250 ??g/L). To facilitate detection of new gill Zn from endogenous gill Zn, the exposure media was significantly enriched with 67 Zn stable isotope (89.60% vs 4.1% natural abundance). Additionally, acute Zn toxicity thresholds (96-h median lethal concentration [LC50]) were determined experimentally through traditional, flow-through toxicity tests in hard water (580 ??g/L) and soft water (110 ??g/L). Following short-term (???3 h) exposures, significant differences in gill accumulation of Zn between hard and soft water treatments were observed at the three common concentrations (75, 150, and 250 ??g/L), with soft water gills accumulating more Zn than hard water gills. Short-term gill Zn accumulation at hard and soft water LC50s (45-min median lethal accumulation) was similar (0.27 and 0.20 ??g/g wet wt, respectively). Finally, comparison of experimental gill Zn accumulation, with accumulation predicted by the biotic ligand model, demonstrated that model output reflected short-term (<1 h) experimental gill Zn accumulation and predicted observed differences in accumulation between hard and soft water rainbow trout gills. Our results indicate that measurable differences exist in short-term gill Zn accumulation following acclimation and exposure in different water hardnesses and that short-term Zn accumulation appears to be predictive of Zn acute toxicity thresholds (96-h LC50s). ?? 2009 SETAC.

Environmental Toxicology and Chemistry

Measurement of total Zn and Zn isotope ratios by quadrupole ICP-MS for evaluation of Zn uptake in gills of brown trout (Salmo trutta) and rainbow trout (Oncorhynchus mykiss)

This study evaluates the potential use of stable zinc isotopes in toxicity studies measuring zinc uptake by the gills of brown trout (Salmo trutta) and rainbow trout (Oncorhynchus mykiss). The use of stable isotopes in such studies has several advantages over the use of radioisotopes, including cost, ease of handling, elimination of permit requirements, and waste disposal. A pilot study using brown trout was performed to evaluate sample preparation methods and the ability of a quadrupole inductively coupled plasma mass spectrometer (ICP-MS) system to successfully measure changes in the 67 Zn/ 66 Zn ratios for planned exposure levels and duration. After completion of the pilot study, a full-scale zinc exposure study using rainbow trout was performed. The results of these studies indicate that there are several factors that affect the precision of the measured 67 Zn/ 66 Zn ratios in the sample digests, including variations in sample size, endogenous zinc levels, and zinc uptake rates by individual fish. However, since these factors were incorporated in the calculation of the total zinc accumulated by the gills during the exposures, the data obtained were adequate for their intended use in calculating zinc binding and evaluating the influences of differences in water quality parameters.

Talanta

Sampling and monitoring for closure

The Metals Mining Sector of the Acid Drainage Technology Initiative (ADTI-MMS) addresses technical drainage-quality issues related to metal mining and related metallurgical operations, for future and active mines, as well as, for historical mines and mining districts. One of the first projects of ADTI-MMS is to develop a handbook describing the best sampling, monitoring, predicting, mitigating, and modeling of drainage from metal mines, pit lakes and related metallurgical facilities based upon current scientific and engineering practices. One of the important aspects of planning a new mine in today's regulatory environment is the philosophy of designing a new or existing mine or expansion of operations for ultimate closure. The holistic philosophy taken in the ADTI-MMS handbook maintains that sampling and monitoring programs should be designed to take into account all aspects of the mine-life cycle. Data required for the closure of the operation are obtained throughout the mine-life cycle, from exploration through post-closure.

Conference Paper

Using imaging spectroscopy to map acidic mine waste

The process of pyrite oxidation at the surface of mine waste may produce acidic water that is gradually neutralized as it drains away from the waste, depositing different Fe-bearing secondary minerals in roughly concentric zones that emanate from mine-waste piles. These Fe-bearing minerals are indicators of the geochemical conditions under which they form. Airborne and orbital imaging spectrometers can be used to map these mineral zones because each of these Fe-bearing secondary minerals is spectrally unique. In this way, imaging spectroscopy can be used to rapidly screen entire mining districts for potential sources of surface acid drainage and to detect acid producing minerals in mine waste or unmined rock outcrops. Spectral data from the AVIRIS instrument were used to evaluate mine waste at the California Gulch Superfund Site near Leadville, CO. Laboratory leach tests of surface samples show that leachate pH is most acidic and metals most mobile in samples from the inner jarosite zone and that leachate pH is near-neutral and metals least mobile in samples from the outer goethite zone.

Environmental Science & Technology

Predictive double-layer modeling of metal sorption in mine-drainage systems

Previous comparison of predictive double-layer modeling and empirically derived metal-partitioning data has validated the use of the double-layer model to predict metal sorption reactions in iron-rich mine-drainage systems. The double-layer model subsequently has been used to model data collected from several mine-drainage sites in Colorado with diverse geochemistry and geology. This work demonstrates that metal partitioning between dissolved and sediment phases can be predictively modeled simply by knowing the water chemistry and the amount of suspended iron-rich particulates present in the system. Sorption on such iron-rich suspended sediments appears to control metal and arsenic partitioning between dissolved and sediment phases, with sorption on bed sediment playing a limited role. At pH > 5, Pb and As are largely sorbed by iron-rich suspended sediments and Cu is partially sorbed; Zn, Cd, and Ni usually remain dissolved throughout the pH range of 3 to 8.

Book chapter

Geochemistry of sediments from coastal marshes of Louisiana

As a part of the U.S. Geological Survey Global Change and Climate History Program we have been studying the biogeochemistry of coastal marshes in Terrebonne Basin, Louisiana. Louisiana has about 40 percent of the coastal wetlands in the conterminous U.S. and it is losing wetlands at one of the highest rates in the U.S. with the conversion of about 65 km2/yr of marsh to open water (Britsch and Dunbar, 1993). The losses have been attributed to human and natural causes including saltwater intrusion through man-made canals, reduced sediment input, and regional subsidence. The net effect of these influences is to change the salinity of interior marshes in a fashion similar to a eustatic sea level rise. We are studying the cycling of carbon, sulfur, and other elements in sediments, waters, and marsh macrophytes in fresh, intermediate/brackish, and saltwater marshes in order to better understand how sea level rise, one aspect of global change, will influence and in turn be influenced by cycling of these elements. By characterizing the critical biogeochemical processes and the recent past environments in these rapidly changing marshes, we can improve predictions of future changes and interpretations of the historic geologic record in similar environments. In this report we describe our coastal marsh study sites in Louisiana, the types of samples collected, the collection methods, the chemical analysis methods, and selected chemical analysis results. Also included are summaries of the project quality control results. The raw chemical analysis results are provided in this report without interpretation. Interpretations will be provided in subsequent reports.

Louisiana

Integrated mineral-resource and mineral-environmental assessments of public lands: Applications for land management and resource planning

Mineral-deposit geology is an important control on natural contamination from unmined mineral deposits, and on the environmental effects of mining and mineral processing. The U. S. Geological Survey, Office of Mineral Resources (USGS/OMR) is now integrating geology-based environmental assessments into its mineral resource assessments of public and other lands. This report presents prototype mineralenvironmental assessments of the State of Colorado and the San Juan National Forest. The following pages will show examples of how geologic information can be used to help predict and prevent adverse environmental effects of mineralresource development.

Colorado

Selectivity and effectiveness of extractants used to release metals associated with organic matter

Partial extraction procedures can be used to release metals associated with organic matter in natural materials. Reagents commonly employed for this purpose include hydrogen peroxide, Na hypochlorite and Na pyrophosphate. This study tested the selectivity of these reagents by comparing the amount of Fe, Mn, Zn and Cu they released from sulfide and oxide minerals and determined the ability of these reagents to release the same metals from peat. Sodium hypochlorite and Na pyrophosphate released between 0.2 and 8.7% of the total metal content of the Fe, Cu and Zn minerals. In contrast, three commonly used hydrogen peroxide reagents released significantly more metals from the oxides and sulfides. Percentages of Zn and Mn released from the peat samples were comparable for all extractions tested. Per cent Cu released from peat by Na pyrophosphate was very low compared to that released by hydrogen peroxide/HNO 3 or na hypochlorite. A smaller fraction of Fe was released from peat by Na hypochlorite than by the other reagents. Iron release by Na hypochlorite correlates with the organic carbon content of the peat samples. A universal extractant for metals associated with organic matter in all types of samples has not been identified. Sodium hypochlorite and Na pyrophosphate are better than hydrogen peroxide in selectively releasing metals bound to organic matter because they do not release significant amounts of metals from oxide and sulfide minerals.

Applied Geochemistry