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R. F. Sanzolone

Publications and source records attributed to R. F. Sanzolone.

At least 19 recordsLinked to original sources
USGS2009

The regional geochemistry of soils and willow in a metamorphic bedrock terrain, Seward Peninsula, Alaska, 2005, and its possible relation to moose

In 2005 willow leaves (all variants of Salix pulchra) and A-, B-, and C-horizon soils were sampled at 10 sites along a transect near the Quarry prospect and 11 sites along a transect near the Big Hurrah mine for the purpose of defining the spatial variability of elements and the regional geochemistry of willow and soil over Paleozoic metamorphic rocks potentially high in cadmium (Cd). Willow, a favorite browse of moose (Alces alces), has been shown by various investigators to bioaccumulate Cd. Moose in this region show clinical signs of tooth wear and breakage and are declining in population for unknown reasons. A trace element imbalance in their diet has been proposed as a possible cause for these observations. Cadmium, in high enough concentrations, is one dietary trace element that potentially could produce such symptoms. We report both the summary statistics for elements in willow and soils and the results of an unbalanced, one-way, hierarchical analysis of variance (ANOVA) (general linear model, GLM), which was constructed to measure the geochemical variability in willow (and soil) at various distance scales across the Paleozoic geologic unit high in bioavailable Cd. All of the geochemical data are presented in the Appendices. The two locations are separated by approximately 80 kilometers (km); sites within a location are approximately 0.5 kilometers apart. Duplicate soil samples collected within a site were separated by 0.05 km or slightly less. Results of the GLM are element specific and range from having very little regional variability to having most of their variance at the top (greater than 80 km) level. For willow, a significant proportion of the total variance occurred at the 'between locations' level for ash yield, barium (Ba), Cd, calcium (Ca), cobalt (Co), nickel (Ni), and zinc (Zn). For soils, concentrations of elements in all three soil horizons were similar in that most of the variability in the geochemical data occurred at the 'between locations' and the 'among sites at a location' GLM levels. Most of the variation in concentrations of Cd in soils occurred among sites (separated by 0.5 km) at both locations across all soil horizons and not between the two locations. Cd distribution across the landscape may be due to variation in soil mineralogy, especially the amount of graphite in soil, which has been associated with Cd. Although samples were collected on the same geologic unit, the geochemistry of soils was demonstrated to be uniform with depth but highly variable between locations separated by 80 km. This exploratory study establishes the presence of elevated levels of Cd in willow growing over Paleozoic bedrock in the Seward Peninsula. Further work is needed to definitively link these high Cd levels in willow browse to the health of moose.

Alaska↗
USGS2008

Substrate Geochemistry and Soil Development in Boreal Forest and Tundra Ecosystems in the Yukon-Tanana Upland and Seward Peninsula, Alaska

We report on soil development as a function of bedrock type and the presence of loess in two high latitude ecosystems (boreal forest and tundra) and from two regions in Alaska?the Yukon-Tanana Upland (YTU, east-central Alaska) and the Seward Peninsula (SP, far-west coastal Alaska). This approach to the study of 'cold soils' is fundamental to the quantification of regional geochemical landscape patterns. Of the five state factors in this study, bedrock and biota (ecosystem; vegetation zone) vary whereas climate (within each area) and topography are controlled. The influence of time is assumed to be controlled, as these soils are thousands of years old (late Quaternary to Holocene). The primary minerals in soils from YTU, developed over loess and crystalline bedrock (metamorphic and intrusive), are quartz, plagioclase, and 2:1 clays; whereas in the SP, where loess and metasedimentary bedrock (schist and quartzite) predominate, they are quartz and muscovite. The A horizon of both regions is rich in peat. Examination of the ratio of mobile (K2O, CaO, and Fe2O3) to immobile (TiO2) major oxides, within each region, shows that very little difference exists in the chemical weathering of soils developed between the two ecosystems examined. Differences were observed between tundra soils developed in the two regions. These differences are most probably due to the dissimilarity in the geochemical importance of both loess and bedrock. A minimal loss of cadmium with soil depth is seen for soils developed over YTU crystalline bedrock in the boreal forest environments. This trend is related to the mobility of cadmium in these soils as well as to its biogenic cycling. Major differences were observed in the proportion of cadmium and zinc among the A, B, and C horizon material sequestered in various soil fractions as measured by sequential soil extractions. These trends followed such variables as the decrease with depth in organic matter, the change in clay minerals, and the change in the proportion of oxides/hydroxides. An analysis of the bulk soil mineralogy and the relation between CaO and MgO and Al2O3 and Fe2O3 indicates that the silty textured soils of the YTU are predominantly eolian (that is, of late Tertiary or Quaternary age) but not broad-regional in origin. Their composition instead is probably the result of locally derived dusts as well as input from long-term, in-place bedrock weathering.

Scientific Investigations Report↗
USGS2007

Geochemical characterization of streambed sediment in the upper Illinois River basin

Geochemistry of fine-fraction streambed sediments collected from the upper Illinois River basin was surveyed in the fall of 1987 as part of the U.S. Geological Survey National Water-Quality Assessment pilot projects. The survey included 567 samples analyzed for 46 elements. Three distinctive distribution patterns were found for seven U.S. Environmental Protection Agency priority pollutants surveyed, as well as for boron and phosphorus: (1) enrichment of elements in the Chicago urban area and in streams draining the urban area relative to rural areas, (2) enrichment in main stems relative to tributaries, and (3) enrichment in low-order streams at high-population-density sites relative to low-population-density sites. Significant differences in background concentrations, as measured by samples from low-order streams, were observed among five subbasins in the study area. Uncertain geochemical correspondence between low-order, background sites and high-order, generally metal enriched sites prevented determination of background levels that would be appropriate for high-order sites. The within-sample ratio of enriched elements was variable within the Chicago area but was constant in the Illinois River downstream from Chicago. Element ratios imply a composite fine-fraction sediment in the Illinois River of 35-40 percent Des Plaines River origin and 60-65 percent Kankakee River origin.

Water Resources Bulletin↗
USGS2007

Sequential Extraction Results and Mineralogy of Mine Waste and Stream Sediments Associated With Metal Mines in Vermont, Maine, and New Zealand

We report results from sequential extraction experiments and the quantitative mineralogy for samples of stream sediments and mine wastes collected from metal mines. Samples were from the Elizabeth, Ely Copper, and Pike Hill Copper mines in Vermont, the Callahan Mine in Maine, and the Martha Mine in New Zealand. The extraction technique targeted the following operationally defined fractions and solid-phase forms: (1) soluble, adsorbed, and exchangeable fractions; (2) carbonates; (3) organic material; (4) amorphous iron- and aluminum-hydroxides and crystalline manganese-oxides; (5) crystalline iron-oxides; (6) sulfides and selenides; and (7) residual material. For most elements, the sum of an element from all extractions steps correlated well with the original unleached concentration. Also, the quantitative mineralogy of the original material compared to that of the residues from two extraction steps gave insight into the effectiveness of reagents at dissolving targeted phases. The data are presented here with minimal interpretation or discussion and further analyses and interpretation will be presented elsewhere.

Open-File Report↗
USGS2006

Preliminary results of sequential extraction experiments for selenium on mine waste and stream sediments from Vermont, Maine, and New Zealand

We report the preliminary results of sequential partial dissolutions used to characterize the geochemical distribution of selenium in stream sediments, mine wastes, and flotation-mill tailings. In general, extraction schemes are designed to extract metals associated with operationally defined solid phases. Total Se concentrations and the mineralogy of the samples are also presented. Samples were obtained from the Elizabeth, Ely, and Pike Hill mines in Vermont, the Callahan mine in Maine, and the Martha mine in New Zealand. These data are presented here with minimal interpretation or discussion. Further analysis of the data will be presented elsewhere.

Open-File Report↗
USGS2003

Chemical analyses of ground and surface waters, Ester Dome, central Alaska, 2000-2001

Water analyses are reported for ground and surface waters collected at 33 sites on and near Ester Dome, Fairbanks area, central Alaska during 2000-2001. This interdisciplinary study focused on documenting the temporal and spatial chemical variations in arsenic concentrations to elucidate the processes that lead to elevated arsenic concentrations in ground water. Field parameters and water analyses are reported for 17 domestic wells, 13 monitoring well sites, and 3 surface water sites. Sampling occurred during November 2000, February 2001, May 2001, July 2001, and September 2001. Waters in the study area are primarily Ca-HCO 3 type, with pH values ranging from 5.97 to 7.87. Dissolved arsenic concentrations ranged from less than 3 to 1160 micrograms per liter.

Alaska↗
USGS1992

Decomposition techniques

Sample decomposition is a fundamental and integral step in the procedure of geochemical analysis. It is often the limiting factor to sample throughput, especially with the recent application of the fast and modern multi-element measurement instrumentation. The complexity of geological materials makes it necessary to choose the sample decomposition technique that is compatible with the specific objective of the analysis. When selecting a decomposition technique, consideration should be given to the chemical and mineralogical characteristics of the sample, elements to be determined, precision and accuracy requirements, sample throughput, technical capability of personnel, and time constraints. This paper addresses these concerns and discusses the attributes and limitations of many techniques of sample decomposition along with examples of their application to geochemical analysis. The chemical properties of reagents as to their function as decomposition agents are also reviewed. The section on acid dissolution techniques addresses the various inorganic acids that are used individually or in combination in both open and closed systems. Fluxes used in sample fusion are discussed. The promising microwave-oven technology and the emerging field of automation are also examined. A section on applications highlights the use of decomposition techniques for the determination of Au, platinum group elements (PGEs), Hg, U, hydride-forming elements, rare earth elements (REEs), and multi-elements in geological materials. Partial dissolution techniques used for geochemical exploration which have been treated in detail elsewhere are not discussed here; nor are fire-assaying for noble metals and decomposition techniques for X-ray fluorescence or nuclear methods be discussed.

Journal of Geochemical Exploration↗
USGS1991

Surface water quality assessment of the Upper Illinois River basin in Illinois, Indiana, and Wisconsin: Geochemical data for fine-fraction streambed sediment from high- and low-order streams, 1987

Geochemical data are presented from a synoptic survey of 46 elements in fine-fraction streambed sediments of the Upper Illinois River Basin during the fall of 1987. The survey was a component study of the Illinois pilot project of the U.S. Geological Survey's National Water-Quality Assessment program. Most of the sampling sites were randomly chosen--135 on main stems of rivers and 238 on first- and second-order streams. In addition, 196 samples were collected for quality-assurance and special-study purposes. The report includes element concentration data and summary-statistics tables of percentiles, nested analysis of variance, and correlation coefficients. All concentration data are included in tabular form and can be selected by map reference number, latitude and longitude, or remark code indicating purpose for collecting sample.

Illinois, Indiana↗
USGS1986

Inductively coupled plasma atomic fluorescence spectrometric determination of cadmium, copper, iron, lead, manganese and zinc

An inductively coupled plasma atomic fluorescence spectrometric method is described for the determination of six elements in a variety of geological materials. Sixteen reference materials are analysed by this technique to demonstrate its use in geochemical exploration. Samples are decomposed with nitric, hydrofluoric and hydrochloric acids, and the residue dissolved in hydrochloric acid and diluted to volume. The elements are determined in two groups based on compatibility of instrument operating conditions and consideration of crustal abundance levels. Cadmium, Cu, Pb and Zn are determined as a group in the 50-ml sample solution under one set of instrument conditions with the use of scatter correction. Limitations of the scatter correction technique used with the fluorescence instrument are discussed. Iron and Mn are determined together using another set of instrumental conditions on a 1-50 dilution of the sample solution without the use of scatter correction. The ranges of concentration (??g g-1) of these elements in the sample that can be determined are: Cd, 0.3-500; Cu, 0.4-500; Fe, 85-250 000; Mn, 45-100 000; Pb, 5-10 000; and Zn, 0.4-300. The precision of the method is usually less than 5% relative standard deviation (RSD) over a wide concentration range and acceptable accuracy is shown by the agreement between values obtained and those recommended for the reference materials.

Journal of Analytical Atomic Spectrometry↗