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Martin B. Goldhaber

Publications and source records attributed to Martin B. Goldhaber.

At least 37 records · Page 2Linked to original sources
USGS2008

Major- and trace-element concentrations in soils from northern California: Results from the Geochemical Landscapes Project pilot study

In 2004, the U.S. Geological Survey (USGS), the Geological Survey of Canada (GSC), and the Mexican Geological Survey (Servicio Geologico Mexicano, or SGM) initiated pilot studies in preparation for a soil geochemical survey of North America called the Geochemical Landscapes Project. The purpose of this project is to provide a better understanding of the variability in chemical composition of soils in North America. The data produced by this survey will be used to construct baseline geochemical maps for regions within the continent. Two initial pilot studies were conducted: (1) a continental-scale study involving a north-south and east-west transect across North America and (2) a regional-scale study. The pilot studies were intended to test and refine sample design, sampling protocols, and field logistics for the full continental soils geochemical survey. Smith and others (2005) reported the results from the continental-scale pilot study. The regional-scale California study was designed to represent more detailed, higher resolution geochemical investigations in a region of particular interest that was identified from the low-sample-density continental-scale survey. A 20,000-km2 area of northern California (fig. 1), representing a wide variety of topography, climate, and ecoregions, was chosen for the regional-scale pilot study. This study area also contains diverse geology and soil types and supports a wide range of land uses including agriculture in the Sacramento Valley, forested areas in portions of the Sierra Nevada, and urban/suburban centers such as Sacramento, Davis, and Stockton. Also of interest are potential effects on soil geochemistry from historical hard rock and placer gold mining in the foothills of the Sierra Nevada, historical mercury mining in the Coast Range, and mining of base-metal sulfide deposits in the Klamath Mountains to the north. This report presents the major- and trace-element concentrations from the regional-scale soil geochemical survey in northern California.

California↗
USGS2007

USGS goals for the coming decade

The U.S. Geological Survey (USGS) proposes six strategic directions for managing ecosystems along with modernization of observation networks of land, water, and biological resources.

Science↗
USGS2005

Major- and trace-element concentrations in soils from two continental-scale transects of the United States and Canada

This report contains major- and trace-element concentration data for soil samples collected from 265 sites along two continental-scale transects in North America. One of the transects extends from northern Manitoba to the United States-Mexico border near El Paso, Tex. and consists of 105 sites. The other transect approximately follows the 38th parallel from the Pacific coast of the United States near San Francisco, Calif., to the Atlantic coast along the Maryland shore and consists of 160 sites. Sampling sites were defined by first dividing each transect into approximately 40-km segments. For each segment, a 1-km-wide latitudinal strip was randomly selected; within each strip, a potential sample site was selected from the most representative landscape within the most common soil type. At one in four sites, duplicate samples were collected 10 meters apart to estimate local spatial variability. At each site, up to four separate soil samples were collected as follows: (1) material from 0-5 cm depth; (2) O horizon, if present; (3) a composite of the A horizon; and (4) C horizon. Each sample collected was analyzed for total major- and trace-element composition by the following methods: (1) inductively coupled plasmamass spectrometry (ICP-MS) and inductively coupled plasma-atomic emission spectrometry (ICPAES) for aluminum, antimony, arsenic, barium, beryllium, bismuth, cadmium, calcium, cerium, cesium, chromium, cobalt, copper, gallium, indium, iron, lanthanum, lead, lithium, magnesium, manganese, molybdenum, nickel, niobium, phosphorus, potassium, rubidium, scandium, silver, sodium, strontium, sulfur, tellurium, thallium, thorium, tin, titanium, tungsten, uranium, vanadium, yttrium, and zinc; (2) cold vapor- atomic absorption spectrometry for mercury; (3) hydride generation-atomic absorption spectrometry for antimony and selenium; (4) coulometric titration for carbonate carbon; and (5) combustion for total carbon and total sulfur.

Open-File Report↗
USGS2004

The geochemical and magnetic record of coal combustion products in West Virginia reservoir sediments and soils

Western West Virginia lies downwind from numerous coal-fired power plants along the Ohio River Valley. To test whether geochemical and mineralogical impacts from these power plants are detectable on the West Virginia landscape, we obtained reservoir cores, soils, and rocks from two separate sites in West Virginia, one in Harrison County (Hinkel and Deegan Reservoirs) and the other in Roane County (Miletree Run Reservoir). Both have small drainage basins that have the effect of maximizing atmospheric inputs relative to weathering inputs. Sediments from Hinkel Reservoir were dated using the 137 Cs method, and by knowledge of the age of the base of the sedimentary section. Major elements in Hinkel Reservoir sediments do not vary systematically over time, suggesting that the depositional history of these sediments has been relatively constant. In contrast, minor elements and sulfur do show dramatic shifts. Zn, Pb, As, S, Cd, Ge, and Hg all peak during the late 1960s and early 1970s. Polyaromatic hydrocarbons associated with combustion processes likewise show this same behavior. Coincident with these maxima is a peak in isothermal remnant magnetization (IRM), a parameter that is proportional to magnetite abundance. We separated the magnetic fraction of the sediments and examined this fraction petrographically. It is dominated by magnetite with a spherical morphology, which is characteristic of magnetite produced by combustion processes. Chemical analyses on local rocks showed that they were not the likely source for the trace element and magnetite enrichments. To compare soils and reservoir sediments, we normalized geochemical data to Ti; the underlying assumption is that Ti will track physical inputs of soil materials into the reservoir sediments. The normalized sediment data for the elements Zn, Pb, As, and S are all higher for sediments deposited during the late 1960s and early 1970s compared to normalized soil data, implying that soils are not the source for the element enrichments. We thus attribute the enrichment to atmospheric inputs. However, a coal-burning zinc smelter within 10 km of the reservoir site that operated until 1971 may have supplied some or all of the anomalous input: There are no nearby major atmospheric pollution sites near Miletree Run Reservoir. A core from this reservoir was dated based on knowledge of the time it was impounded. Like Hinkel Reservoir, there are no systematic shifts in major element contents over its depositional history. Like Hinkel Reservoir, there are also significant shifts in trace elements and IRM that cannot be explained by local soil sources. Magnetic separates from this reservoir are also dominated by spherical combustion-produced magnetite. Covariance over the period 1930-1980 between magnetite and sulfur with US SO 2 production (which comes dominantly from coal combustion) is strongly suggestive of a significant atmospheric input into Miletree Run Reservoir sediments. The nearest upwind power plants are between 50 and 75 km distant. Thus, relatively long distance transmission of particulate matter from the power plants of the Ohio River Valley is likely in this case.

West Virginia↗
USGS2003

Trace-metal sources and their release from mine wastes: examples from humidity cell tests of hardrock mine waste and from Warrior Basin coal

To assess the potential impact of metal and acid contamination from mine-waste piles, it is important to identify the mineralogic source of trace metals and their mode of occurrence. Microscopic analysis of mine-waste samples from both hard-rock and coalmine waste samples demonstrate a microstructural control, as well as mineralogic control, on the source and release of trace metals into local water systems. The samples discussed herein show multiple periods of sulfide mineralization with varying concentrations of trace metals. In the first case study, two proprietary hard-rock mine-waste samples exposed to a series of humidity cell tests (which simulate intense chemical weathering conditions) generated acid and released trace metals. Some trace elements of interest were: arsenic (45-120 ppm), copper (60-320 ppm), and zinc (30-2,500 ppm). Untested and humidity cell-exposed samples were studied by X-ray diffraction, scanning electron microscope with energy dispersive X-ray (SEM/EDX), and electron microprobe analysis. Studies of one sample set revealed arsenic-bearing pyrite in early iron- and magnesium-rich carbonate-filled microveins, and iron-, copper-, arsenic-, antimony-bearing sulfides in later crosscutting silica-filled microveins. Post humidity cell tests indicated that the carbonate minerals were removed by leaching in the humidity cells, exposing pyrite to oxidative conditions. However, sulfides in the silica-filled veins were more protected. Therefore, the trace metals contained in the sulfides within the silica-filled microveins may be released to the surface and (or) ground water system more slowly over a greater time period. In the second case study, trace metal-rich pyrite-bearing coals from the Warrior Basin, Alabama were analyzed. Arsenic-bearing pyrite was observed in a late-stage pyrite phase in microfaults and microveins that crosscut earlier arsenic.

Conference Paper↗
USGS2002

Arsenic in rocks and stream sediments of the central Appalachian Basin, Kentucky

Arsenic (As) enrichment in coal and stream sediments has been documented in the southern Appalachian basin (see Goldhaber and others, submitted) and is attributed to interaction of rocks and coal with metamorphic fluids generated during the Allegheny Orogeny (late Paleozoic). Similarly derived fluids are expected to affect the coal and in the Kentucky Appalachian Basin to the north as well. In addition, similar processes may have influenced the Devonian oil shale on the western margin of the basin. The major goals of this study are to determine the effect such fluids had on rocks in the Kentucky Appalachian basin (fig. 1), and to understand the geochemical processes that control trace-metal source, residence, and mobility within the basin. This report includes data presented in a poster at the USGS workshop on arsenic (February 21 and 22, 2001), new NURE stream sediment data3 , and field data from a trip in April 2001. Although data for major and minor elements and all detectable trace metals are reported in the Appendices, the narrative of this report primarily focuses on arsenic.

Kentucky↗
USGS2002

Geologic cross sections showing the concentrations of As, Cd, Co, Cu, Cr, Fe, Mo, Ni, Pb, and Zn in acid-insoluble residues of Paleozoic rocks within the Doniphan/Eleven Point Ranger District of the Mark Twain National Forest, Missouri, USA

This report is a product of a U.S. Geological Survey investigation that is focused on characterizing the potential environmental impacts of lead-zinc mining within the Doniphan/Eleven Point ranger district of the Mark Twain national forest. The elemental concentrations of iron (Fe), arsenic (As), cadmium (Cd), cobalt (Co), copper (Cu), chromium (Cr), nickel (Ni), lead (Pb), and zinc (Zn) in acidinsoluble residues are shown for boreholes along two geologic cross sections within Doniphan/Elevan Point ranger district (Figure 1). The purpose of this report is to characterize, in a general sense, the distribution of economically and environmentally important elements within the rocks and aquifers of the Doniphan/Eleven Point ranger district

Missouri↗
USGS2000

Distribution of a suite of elements including arsenic and mercury in Alabama coal

Arsenic and other elements are unusually abundant in Alabama coal. This conclusion is based on chemical analyses of coal in the U.S. Geological Survey's National Coal Resources Data System (NCRDS; Bragg and others, 1994). According to NCRDS data, the average concentration of arsenic in Alabama coal (72 ppm) is three times higher than is the average for all U.S. coal (24 ppm). Of the U.S. coal analyses for arsenic that are at least 3 standard deviations above the mean, approximately 90% are from the coal fields of Alabama. Figure 1 contrasts the abundance of arsenic in coal of the Warrior field of Alabama (histogram C) with that of coal of the Powder River Basin, Wyoming (histogram A), and the Eastern Interior Province including the Illinois Basin and nearby areas (histogram B). The Warrior field is by far the largest in Alabama. On the histogram, the large 'tail' of very high values (> 200 ppm) in the Warrior coal contrasts with the other two regions that have very few analyses greater than 200 ppm.

Alabama↗
USGS1999

Mechanical and thermal control of cleating and shearing in coal: examples from the Alabama coalbed methane field, USA

Natural fractures provide most of the interconnected macroporosity in coal. Therefore, understanding the characteristics of these fractures and the associated mechanisms of formation is essential for effective coalbed methane exploration and field management. Natural fractures in coal can be divided into two general types: cleat and shear structures. Cleat has been studied for more than a century, yet the mechanisms of cleat formation remain poorly understood (see reviews by Close, 1993; Laubach et al .,1998). An important aspect of cleating is that systematic fracturing of coal is takes place in concert with devolatization and concomitant shrinkage of the coal matrix during thermal maturation (Ammosov and Eremin, 1960). Coal, furthermore, is a mechanically weak rock type that is subject to bedding-plane shear between more competent beds like shale, sandstone, and limestone. Yet, the significance of shear structures in coal has only begun to attract scientific interest (Hathaway and Gayer, 1996; Pashin, 1998).

Alabama↗
USGS1997

Regional diagenetic patterns in the St. Peter Sandstone; implications for brine migration in the Illinois Basin

Diagenetic minerals and alteration patterns in the Ordovician St. Peter Sandstone, Illinois Basin, record varied hydrologic and chemical conditions during the basin?s long and complex geologic history. Major diagenetic events modifying the St. Peter Sandstone include (1) mechanical compaction, (2) early K-feldspar overgrowth and dolospar precipitation, (3) burial quartz, dolospar, anhydrite, and calcite cementation, and (4) carbonate-cement and K-feldspar grain dissolution. Radiometric age dates of authigenic K-feldspar and illite in combination with the reconstructed burial history of the St. Peter reveal that early-diagenetic K-feldspar and dolospar precipitated at shallow to moderate depths in the Devonian, whereas late-diagenetic quartz, dolospar, anhydrite, and calcite formed during deep burial in the Late Pennsylvanian to Early Permian. Stable-isotope geochemistry and fluid-inclusion paleothermometry suggest that burial cements precipitated from saline fluids over a wide temperature range. In the southern part of the basin, burial cements preserve a record of diagenetic effects that were in part controlled by fractures and hydrothermal-fluid circulation. Baroque dolospar cementation is the most significant of these effects.

Bulletin↗
USGS1997

Paleomagnetic and 40Ar/39Ar results from the Grant intrusive breccia and comparison to the Permian Downeys Bluff sill — Evidence for Permian igneous activity at Hicks Dome, southern Illinois Basin

Igneous processes at Hicks dome, a structural upwarp at lat 37.5° N., long 88.4° W. in the southern part of the Illinois Basin, may have thermally affected regional basinal fluid flow and may have provided fluorine for the formation of the Illinois-Kentucky Fluorspar district. The timing of both igneous activity and mineralization is poorly known. For this reason, we have dated an intrusive breccia at Hicks dome, the Grant intrusion, using 40 Ar/ 39 Ar geochronometric and paleomagnetic methods. Concordant plateau dates, giving Permian ages, were obtained from amphibole (272.1±0.7 [1σ] Ma) and phlogopite (272.7±0.7 [1σ] Ma). After alternating-field (AF) demagnetization, specimens that contain titanomagnetite-bearing igneous rock fragments give a mean remanent direction of declination (D)=168.4°; inclination (I)=–8°; α95=8.6°; number of specimens (N)=10; this direction yields a virtual geomagnetic pole (VGP) at lat 54.8° N., long 119.0° E., δp=4.4°, δm=8.7°, near the late Paleozoic part of the North American apparent pole wander path. A nearly identical magnetization was found for the nearby Downeys Bluff sill (previously dated at about 275±24 Ma by the Rb-Sr method), in southern Illinois. Both AF and thermal demagnetization isolated shallow, southeasterly remanent directions carried by magnetite in the sill and from pyrrhotite in the baked contact of the Upper Mississippian Downeys Bluff Limestone: D=158.6°; I=–11.8°; α95=3.8°; N=15, yielding a VGP at lat 53.0° N., long 128.7° E., δp=2.0°, δm=3.9°. The paleomagnetic results, isotopic dates, and petrographic evidence thus favor the acquisition of thermal remanent magnetization by the Grant breccia and the Downeys Bluff sill during the Permian. The isotopic dates record rapid cooling from temperatures greater than 550°C to less than 300°C (the closure temperatures for diffusion of 40Ar in amphibole and phlogopite, respectively) after emplacement during the Permian. The results further indicate that individual clasts of the Grant breccia were emplaced at temperatures greater than about 550°C, the magnetization-blocking temperature of the titanomagnetite in the breccia, and that it cooled very rapidly, within less than 1–2 m.y. After cooling, the breccia was not affected by thermal perturbations greater than about 300°C.

Illinois, Kentucky↗
USGS1996

Fluid inclusions and biomarkers in the Upper Mississippi Valley zinc-lead district; implications for the fluid-flow and thermal history of the Illinois Basin

The Upper Mississippi Valley zinc-lead district is hosted by Ordovician carbonate rocks at the northern margin of the Illinois Basin. Fluid inclusion temperature measurements on Early Permian sphalerite ore from the district are predominantly between 90?C and I50?C. These temperatures are greater than can be explained by their reconstructed burial depth, which was a maximum of approximately 1 km at the time of mineralization. In contrast to the temperatures of mineral formation derived from fluid inclusions, biomarker maturities in the Upper Mississippi Valley district give an estimate of total thermal exposure integrated over time. Temperatures from fluid inclusions trapped during ore genesis with biomarker maturities were combined to construct an estimate of the district's overall thermal history and, by inference, the late Paleozoic thermal and hydrologic history of the Illinois Basin. Circulation of groundwater through regional aquifers, given sufficient flow rates, can redistribute heat from deep in a sedimentary basin to its shallower margins. Evidence for regional-scale circulation of fluids is provided by paleomagnetic studies, regionally correlated zoned dolomite, fluid inclusions, and thermal maturity of organic matter. Evidence for igneous acti vity contemporaneous with mineralization in the vicinity of the Upper Mississippi Valley district is absent. Regional fluid and heat circulation is the most likely explanation for the elevated fluid inclusion temperatures (relative to maximum estimated burial depth) in the Upper Mississippi Valley district. One plausible driving mechanism and flow path for the ore-forming fluids is groundwater recharge in the late Paleozoic Appalachian-Ouachita mountain belt and northward flow through the Reelfoot rift and the proto- Illinois Basin to the Upper Mississippi Valley district. Warm fluid flowing laterally through Cambrian and Ordovician aquifers would then move vertically upward through the fractures that control sphalerite mineralization in the Upper Mississippi Valley district. Biomarker reactant-product measurements on rock extracts from the Upper Mississippi Valley district define a relatively low level ofthermal maturity for the district, 0.353 for sterane and 0.577 for hopane. Recently published kinetic constants permit a time-temperature relationship to be determined from these biomarker maturities. Numerical calculations were made to simulate fluid heat flow through the fracture-controlled ore zones of the Thompson-Temperly mine and heat transfer to the adjacent rocks where biomarker samples were collected. Calculations that combine the fluid inclusion temperatures and the biomarker constraints on thermal maturity indicate that the time interval during which mineralizing fluids circulated through the Upper Mississippi Valley district is on the order of 200,000 years. Fluid inclusion measurements and thermal maturities from biomarkers in the district reflect the duration of peak temperatures resulting from regional fluid circulation. On the basis of thermal considerations, the timing of fluorite mineralization in southern Illinois, and the northward-decreasing pattern of fluorine enrichment in sediments, we hypothesize that the principal flow direction was northward through the Cambrian and Ordovician aquifers of the Illinois Basin. A basin-scale flow system would result in mass transport (hydrocarbon migration, transport of metals in solution) and energy (heat) transport, which would in turn drive chemical reactions (for example, maturation of organic matter, mineralization, diagenetic reactions) within the Illinois Basin and at its margins.

Bulletin↗