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Robert R. Seal,

Publications and source records attributed to Robert R. Seal,.

25 records · Page 2Linked to original sources
USGS2015

Sediment-hosted stratabound copper deposit model

This report contains a descriptive model of sediment-hosted stratabound copper (SSC) deposits that supersedes the model of Cox and others (2003). This model is for use in assessments of mineral resource potential. SSC deposits are the second most important sources of copper in the world behind porphyry copper deposits. Around 20 percent of the copper in the world is produced from this class of deposits. They are also the most important sources of cobalt in the world, and they are fourth among classes of ore deposits in production of silver. SSC deposits are the basis of the economies of three countries: Democratic Republic of Congo, Poland, and Zambia. This report provides a description of the key features of SSC deposits; it identifies their tectonic-sedimentary environments; it illustrates geochemical, geophysical, and geoenvironmental characteristics of SSC deposits; it reviews and evaluates hypotheses on how these deposits formed; it presents exploration and assessment guides; and it lists some gaps in our knowledge about the SSC deposits. A summary follows that provides overviews of many subjects concerning SSC deposits.

Scientific Investigations Report↗
USGS2013

Stable isotopes in mid-ocean ridge hydrothermal systems: Interactions between fluids, minerals, and organisms

Studies of abundance variations of light stable isotopes in nature have had a tremendous impact on all aspects of geochemistry since the development, in 1947, of a gas source isotope ratio mass spectrometer capable of measuring small variations in stable isotope ratios (Nice, 1947]. Stable isotope geochemistry is now a mature field, as witnessed by the proliferation of commercially available mass spectrometers installed at virtually every major academic, government, and private-sector research geochemistry laboratory. A recent search of a literature database revealed over 3,000 articles that utilized stable isotope geochemistry over the last 20 years. Nonetheless, many exciting new technical developments are leading to exciting new discoveries and applications. In particular, micro-analytical techniques involving new generations of laser- and ion-microprobes are revolutionizing the types of analyses that can be done on spot sizes as small as a few tens of micrometers [Shanks and Criss, 1989]. New generations of conventional gas source and thermal ionization mass spectrometers, with high levels of automation and increased sensitivity and precision, are allowing analyses of large numbers of samples, like those needed for stable isotope stratigraphy in marine sediments, and are enabling the development and application of new isotopic systems.

Book chapter↗
USGS2005

Geochemistry of sulfate minerals in high- and low-temperature environments: A tribute to Robert O. Rye

This special issue is a tribute to Robert O. Rye, known as "Bob" to most, in light of his highly productive and ongoing career. Almost all of the papers in this issue are derived from topical sessions on sulfate minerals in hydrothermal and low-temperature environments. The sessions, held at the 2000 Geological Society of America meeting in Reno, NV, and sponsored jointly by the Mineralogical Society of America, the Society of Economic Geologists and the Geochemical Society, included 29 oral and 9 poster presentations. The sessions complemented a short course on the crystallography, geochemistry and environmental significance of sulfate minerals, sponsored by the Mineralogical Society of America and the Geochemical Society, which immediately preceded the meeting (Alpers et al., 2000). The 23 papers in this special issue typify the breadth of Bob Rye’s research in this important area of geochemistry.

Chemical Geology↗
USGS2001

Sulfur and lead isotope geochemistry of hypogene mineralization at the Barite Hill Gold Deposit, Carolina Slate Belt, southeastern United States: A window into and through regional metamorphism

The Barite Hill gold deposit, at the southwestern end of the Carolina slate belt in the southeastern United States, is one of four gold deposits in the region that have a combined yield of 110 metric tons of gold over the past 10 years. At Barite Hill, production has dominantly come from oxidized ores. Sulfur isotope data from hypogene portions of the Barite Hill gold deposit vary systematically with pyrite–barite associations and provide insights into both the pre-metamorphic Late Proterozoic hydrothermal and the Paleozoic regional metamorphic histories of the deposit. The δ 34 S values of massive barite cluster tightly between 25.0 and 28.0‰, which closely match the published values for Late Proterozoic seawater and thus support a seafloor hydrothermal origin. The δ 34 S values of massive sulfide range from 1.0 to 5.3‰ and fall within the range of values observed for modern and ancient seafloor hydrothermal sulfide deposits. In contrast, δ 34 S values for finer-grained, intergrown pyrite (5.1–6.8‰) and barite (21.0–23.9‰) are higher and lower than their massive counterparts, respectively. Calculated sulfur isotope temperatures for the latter barite–pyrite pairs (Δ=15.9–17.1‰) range from 332–355 °C and probably reflect post-depositional equilibration at greenschist-facies regional metamorphic conditions. Thus, pyrite and barite occurring separately from one another provide pre-metamorphic information about the hydrothermal origin of the deposit, whereas pyrite and barite occurring together equilibrated to record the metamorphic conditions. Preliminary fluid inclusion data from sphalerite are consistent with a modified seawater source for the mineralizing fluids, but data from quartz and barite may reflect later metamorphic and (or) more recent meteoric water input. Lead isotope values from pyrites range for 206 Pb/ 204 Pb from 18.005–18.294, for 207 Pb/ 204 Pb from 15.567–15.645, and for 208 Pb/ 204 Pb from 37.555–38.015. The data indicate derivation of the ore leads from the country rocks, which themselves show evidence for contributions from relatively unradiogenic, mantle-like lead, and more evolved or crustal lead. Geological relationships, and stable and radiogenic isotopic data, suggest that the Barite Hill gold deposit formed on the Late Proterozoic seafloor through exhalative hydrothermal processes similar to those that were responsible for the massive sulfide deposits of the Kuroko district, Japan. On the basis of similarities with other gold-rich massive sulfide deposits and modern seafloor hydrothermal systems, the gold at Barite Hill was probably introduced as an integral part of the formation of the massive sulfide deposit.

Georgia, North Carolina, South Carolina, Virginia↗
USGS2001

The Gibbs free energy of nukundamite (Cu3.38Fe0.62S4): A correction and implications for phase equilibria

The Gibbs free energy of formation of nukundamite (Cu 3.38 Fe 0.62 S 4 ) was calculated from published experimental studies of the reaction 3.25 Cu 3.38 Fe 0.62 S 4 + S 2 = 11 CuS + 2 FeS 2 in order to correct an erroneous expression in the published record. The correct expression describing the Gibbs free energy of formation (kJ·mol −1 ) of nukundamite relative to the elements and ideal S 2 gas is Δ f G° nukundamite, T(K) = −549.75 + 0.23242 T + 3.1284 T 0.5 , with an uncertainty of 0.6%. An evaluation of the phase equilibria of nukundamite with associated phases in the system Cu–Fe–S as a function of temperature and sulfur fugacity indicates that nukundamite is stable from 224 to 501°C at high sulfidation states. At its greatest extent, at 434°C, the stability field of nukundamite is only 0.4 log f (S 2 ) units wide, which explains its rarity. Equilibria between nukundamite and bornite, which limit the stability of both phases, involve bornite compositions that deviate significantly from stoichiometric Cu 5 FeS 4 . Under equilibrium conditions in the system Cu–Fe–S, nukundamite + chalcopyrite is not a stable assemblage at any temperature.

Canadian Mineralogist↗
USGS1999

Environmental processes that affect mineral deposits in the eastern United States

A thorough understanding of the environmental processes that affect mineral deposits and mine wastes has become increasingly important as the Nation wrestles with how to meet our current demand for metals without compromising the environment and how to mitigate the damage caused by the mining practices of previous generations. Regulatory requirements are dominated by empirical approaches to environmental problems associated with mining, but mitigation and reclamation can be enhanced greatly by a theoretical and conceptual understanding of the processes that affect the availability, transport, and fixation of metals and the generation of acidic waters. U.S. Geological Survey (USGS) research efforts in the Eastern United States are concentrating on environmental processes that affect a class of mineral deposits known as massive sulfide deposits. These occurrences were valued historically for their sulfur content and recently for their metals. This deposit type is a research priority because of its economic significance and high potential for adverse environmental impact due to its high sulfide content and the low acid-buffering capacity of host rocks. Numerous examples of these deposits are found in the East, including reclaimed mine sites, abandoned mines, active mines, and sites currently in the permitting process for future production. Published studies of mine drainage chemistry from the Iron Mountain massive sulfide deposit in California have documented extreme conditions of very low pH and high heavy-metal concentrations. These extreme conditions are attributed to the unique hydrologic and climatic settings of the deposit and probably are independent of the mineral deposit type. Areas currently under study include Bald Mountain, Maine, the Great Smoky Mountains National Park, the Vermont copper belt, Contrary Creek, Virginia, and Prince William Forest Park, Virginia (fig.1). Goals of the research are (1) to give land-use planners and the mining industry a better empirical framework from which to assess potential environmental impacts of mining, particularly under eastern climatic conditions, and (2) to provide a better theoretical and conceptual framework from which to design more effective and cost efficient mitigation and reclamation programs.

Information Handout↗
USGS1999

Stable isotopes and mineral resource investigations in the United States

The elements oxygen, hydrogen, sulfur, and carbon are important constituents of hydrothermal ore-forming systems and the weathering processes of mineral deposits in the surficial environment. They also play key roles in volcanic activity, ecosystem dynamics, climate change, and hydrologic and atmospheric processes. Therefore, study of the stable isotopes of these elements can provide powerful insights into these processes. This is especially true for ongoing U.S. Geological Survey (USGS) projects in the Eastern United States that are concerned with the origins of base (copper, lead, and zinc) and precious (gold and silver) metal deposits in the Carolina slate belt and northern Maine and with the environmental effects of weathering of mineral deposits (fig. 1).

Information Handout↗