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Geology topics

D. B. Smith

Publications and source records attributed to D. B. Smith.

At least 37 records · Page 2Linked to original sources
USGS2003

Scale-dependent temporal variations in stream water geochemistry

A year-long study of four western Montana streams (two impacted by mining and two “pristine”) evaluated surface water geochemical dynamics on various time scales (monthly, daily, and bi-hourly). Monthly changes were dominated by snowmelt and precipitation dynamics. On the daily scale, post-rain surges in some solute and particulate concentra tions were similar to those of early spring runoff flushing characteristics on the monthly scale. On the bi-hourly scale, we observed diel (diurnal−nocturnal) cycling for pH, dissolved oxygen, water temperature, dissolved inorganic carbon, total suspended sediment, and some total recoverable metals at some or all sites. A comparison of the cumulative geochemical variability within each of the temporal groups reveals that for many water quality parameters there were large overlaps of concentration ranges among groups. We found that short-term (daily and bi-hourly) variations of some geochemical parameters covered large proportions of the variations found on a much longer term (monthly) time scale. These results show the importance of nesting short-term studies within long-term geochemical study designs to separate signals of environmental change from natural variability.

Montana↗
USGS2003

Biosolids, soils, ground-water, and streambed-sediment data for a biosolids-application area near Deer Trail, Colorado, 1999

In January 1999, the U.S. Geological Survey began an expanded monitoring program near Deer Trail, Colorado, in cooperation with the Metro Wastewater Reclamation District and the North Kiowa Bijou Groundwater Management District. Monitoring components were biosolids, soils, crops, ground water, and streambed sediments. The monitoring program addresses concerns from the public about chemical effects from applications of biosolids to farmland in the Deer Trail, Colorado, area. Constituents of primary concern to the public are arsenic, cadmium, chromium, copper, lead, mercury, molybdenum, nickel, selenium, zinc, plutonium, and gross alpha and beta activity and are included for all monitoring components. This report presents chemical data from the first year of the monitoring program, January?December 1999, for biosolids, soils, alluvial and bedrock ground water, and streambed sediments. The groundwater section of this report also includes climate data, lithologic descriptions, well-completion diagrams, water levels, summary statistics for the water-quality data, and results of statistical testing of selected data for trends and for exceedance of Colorado regulatory standards. Data in this report provide a geochemical baseline for each monitoring component prior to the planned water transfer in 2000 from the Lowry Landfill Superfund site to Metro Wastewater Reclamation District treatment facilities.

Colorado↗
USGS2001

Geochemical landscapes of the conterminous United States — New map presentations for 22 elements

Geochemical maps of the conterminous United States have been prepared for seven major elements (Al, Ca, Fe, K, Mg, Na, and Ti) and 15 trace elements (As, Ba, Cr, Cu, Hg, Li, Mn, Ni, Pb, Se, Sr, V, Y, Zn, and Zr). The maps are based on an ultra low-density geochemical survey consisting of 1,323 samples of soils and other surficial materials collected from approximately 1960-1975. The data were published by Boerngen and Shacklette (1981) and black-and-white point-symbol geochemical maps were published by Shacklette and Boerngen (1984). The data have been reprocessed using weighted-median and Bootstrap procedures for interpolation and smoothing.

Conterminous United States↗
USGS2000

National Geochemical Database, U.S. Geological Survey RASS (Rock Analysis Storage System) geochemical data for Alaska

This dataset contains geochemical data for Alaska produced by the analytical laboratories of the Geologic Division of the U.S. Geological Survey (USGS). These data represent analyses of stream-sediment, heavy-mineral-concentrate (derived from stream sediment), soil, and organic material samples. Most of the data comes from mineral resource investigations conducted in the Alaska Mineral Resource Assessment Program (AMRAP). However, some of the data were produced in support of other USGS programs. The data were originally entered into the in-house Rock Analysis Storage System (RASS) database. The RASS database, which contains over 580,000 data records, was used by the Geologic Division from the early 1970's through the late 1980's to archive geochemical data. Much of the data have been previously published in paper copy USGS Open-File Reports by the submitter or the analyst but some of the data have never been published. Over the years, USGS scientists recognized several problems with the database. The two primary issues were location coordinates (either incorrect or lacking) and sample media (not precisely identified). This dataset represents a re-processing of the original RASS data to make the data accessible in digital format and more user friendly. This re-processing consisted of checking the information on sample media and location against the original sample submittal forms, the original analytical reports, and published reports. As necessary, fields were added to the original data to more fully describe the sample preparation methods used and sample medium analyzed. The actual analytical data were not checked in great detail, but obvious errors were corrected.

Alaska↗
USGS1998

Electrogeochemical sampling with NEOCHIM - results of tests over buried gold deposits

Electrogeochemical extraction methods are based on the migration of ions in an electric field. Ions present in soil moisture are transported by an applied current into fluids contained in special electrodes placed on the soil. The fluids are then collected and analyzed. Extractions are governed by Faraday's and Ohm's laws and are modeled by the operation of a simple Hittord transference apparatus. Calculations show that the volume of soil sampled in an ideal electrogeochemical extraction can be orders of magnitude greater than the volumes used in more popular geochemical extraction methods, although this has not been verified experimentally. CHIM is a method of in-situ electrogeochemical extraction that was developed in the former Soviet Union and has been tested and applied internationally to exploration for buried mineral deposits. Tests carried out at the US Geological Survey (USGS) indicated that there were problems inherent in the use of CHIM technology. The cause of the problems was determined to be the diffusion of acid from the conventional electrode into the soil. The NEOCHIM electrode incorporates two compartments and a salt bridge in a design that inhibits diffusion of acid and enables the collection of anions or cations. Tests over a gold-enriched vein in Colorado and over buried, Carlin-type, disseminated gold deposits in northern Nevada show that there are similarities and differences between NEOCHIM results and those by partial extractions of soils which include simple extractions with water, dilute acids and solutions of salts used as collector fluids in the electrodes. Results of both differ from the results obtained by total chemical digestion. The results indicate that NEOCHIM responds to mineralized faults associated with disseminated gold deposits whereas partial and total chemical extraction methods do not. This suggests that faults are favored channels for the upward migration of metals and that NEOCHIM may be more effective in exploration for the deposits. It defines anomalies that are often narrow and intense, an observation previously made by CHIM researchers. The field tests show that NEOCHIM is less affected by surface contamination. A test over the Mike disseminated gold deposit indicates that the method may not be effective for locating deposits with impermeable cover. Faradaic extraction efficiencies of 20-30%, or more, are frequently achieved with NEOCHIM and the method generally shows good reproducibility, especially in extraction of major cations. However, ions of other metals that are useful in exploration, including Au and As, may be collected in low and temporally variable concentrations. The reason for this variability is unclear and requires further investigation.CHIM is a method of in-situ electrogeochemical extraction developed for the exploration of buried mineral deposits. However, electrode problems like diffusion of acid into the soil were encountered during the use of CHIM. The NEOCHIM electrode was developed to inhibit the diffusion of acid and enable collection of anions or cations. Tests over buried gold deposits showed that NEOCHIM responds to mineralized faults associated with disseminated gold deposits whereas partial and total chemical extraction methods do not. This suggests that faults are favored channels for the upward migration of metals and NEOCHIM may be effective in exploration for the deposits. But ions of metals may be collected in low and variable concentration.

Journal of Geochemical Exploration↗
USGS1993

Preliminary studies of the CHIM electrogeochemical method at the Kokomo Mine, Russell Gulch, Colorado

The CHIM electrogeochemical exploration technique was developed in the former Soviet Union about 20 years ago and is claimed to be effective in exploration for concealed mineral deposits that are not detectable by other geochemical or geophysical techniques. The method involves providing a high-voltage direct current to an anode and an array of special collector cathodes. Cations mobile in the electric field are collected at the cathodes and their concentrations determined. The U.S. Geological Survey started a study of the CHIM method by conducting tests over a precious- and base-metal-bearing quartz vein covered with 3 m of colluvial soil and weathered bedrock near the Kokomo Mine, Colorado. The tests show that the CHIM method gives better definition of the vein than conventional soil geochemistry based on a total-dissolution technique. The CHIM technique gives reproducible geochemical anomaly patterns, but the absolute concentrations depend on local site variability as well as temporal variations. Weak partial dissolutions of soils at the Kokomo Mine by an enzyme leach, a dilute acetic acid leach, and a dilute hydrochloric acid leach show results comparable to those from the CHIM method. This supports the idea that the CHIM technique is essentially a weak in-situ partial extraction involving only ions able to move in a weak electric field.

Journal of Geochemical Exploration↗
USGS1993

The Hatu gold anomaly, Xinjiang-Uygur Autonomous Region, China - testing the hypothesis of aeolian transport of gold

In 1987, a cooperative project between the U.S. Geological Survey and the Institute of Geophysical and Geochemical Exploration was initiated to evaluate the origin of the Hatu gold anomaly. The anomaly is located in the Hatu mining district in the northwest corner of Xinjiang-Uygur Autonomous Region in northwest China. The climate is semiarid to arid and wind erosion predominates. A regional soil survey of the Hatu district, based on samples collected on a 200 by 500 m grid and composited prior to chemical analysis to a density of one sample per square km, delineated a series of south-southeast-trending Au anomalies. Anomalous Au values range from 5 ppb to more than 700 ppb. The Hatu anomaly, the most prominent of these anomalies, is more than 30 km long and about 5 km wide. The mining town of Hatu and the economic gold deposits of Qiqu 1 and Qiqu 2 are at the northern end of this anomaly. The axis of the Hatu anomaly cuts across mapped structure and stratigraphy in the district, but is parallel to the prevailing wind direction. This observation led to the hypothesis that the Hatu anomaly is the result of acolian dispersion of gold from the vicinity of Qiqu 1 and Qiqu 2. The alternative interpretation, that the anomalies reflected additional primary gold occurrences, was not consistent with existing information on the known occurrences and the geology.

Journal of Geochemical Exploration↗