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Bruce R. Doe

Publications and source records attributed to Bruce R. Doe.

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Further considerations of the Ce/Yb vs. Ba/Ce plot in volcanology and tectonics

A plot of Ce/Yb vs. Ba/Ce, for locality averages, effectively separates mid-ocean ridge basalts (MORB) (Ce/Yb <10, Ba/Ce 1-4.2), oceanic island volcanics (OIV) (Ce/Yb >10, Ba/Ce <6), which are generally hotspot related, and island arc volcanics (IAV) (Ce/Yb <23, Ba/Ce >4.2). The conventional interpretation is that these three types of volcanic environments involve oceanic rift-related, large-volume partial melts (˜20-30%) of a depleted source (MORB), small volume melts (˜5% for alkalic volcanics) of enriched sources related to plumes (OIV), and melts of hydrous-enriched sources during subduction, especially for Ba (IAV). Three OIV sites, however, have average ratios that fall in the MORB field (e.g., Krafla Volcano, Iceland), and these localities also tend to have other geochemical data similar to MORB. Average ratios of Hawaiian tholeiitic shield basalts of Mauna Kea and Koolau volcanoes occupy a restricted field on a plot of Ce/Yb vs. Ba/Ce of 10-18 for Ce/Yb and 2.8-3.1 for Ba/Ce, a field toward which other shield basalts and cone-building volcanics regress. In general, post-shield alkalic rocks have higher values of Ce/Yb than do tholeiites. Peralkalic basalts (basanites, melilitites, and phonolites) have even higher values of Ce/Yb, reflecting smaller degrees of partial melting (perhaps 1-2%) and melting of sources containing phlogopite that were enriched by CO 2 -dominated fluids. The minor post-erosion nephelinitic suites of Hawaii (e.g., the Honolulu Series on Oahu, and the Koloa suite on Kauai) generally have values both greater than IAV for Ce/Yb and greater than other kinds of OIV for Ba/Ce in a part of the plot previously not found to be occupied by data. Alkali basalts of both these nephelinitic series have the lowest and similar ratios (Ce/Yb ˜ 25; Ba/Ce ˜ 10). In the Hawaiian Islands, there are two trends. One (a), where phlogopite has been interpreted to remain in the source, generally has Ba/Ce decrease away from the alkali basalts as Ce/Yb increases. The other (b), where phlogopite has been interpreted to enter the melt, occupies a field that is high in both Ce/Yb (>30) relative to IAV and in Ba/Ce (>8) relative to the OIV field. There are some exceptions, also, for IAV that plot outside the IAV field. The values of Ce/Yb in Mariana Islands samples, for example, are exceptionally low for the IAV (Ce/Yb <5 with many samples <2). Examples of two cross-chain Kasuga Islands, however, have average values of Ce/Yb considerably greater than for any other Mariana Islands data, and individual samples extend from within the IAV field into the OIV field, which may indicate a mixture of IAV and OIV sources (rather than involvement of a hotspot, these island volcanics have been interpreted as magma of OIV entrapped "plums" in an IAV "pudding" by Stern et al., 1993). Not surprisingly, continental arc volcanics (CAV) are generally similar to IAV, but with somewhat greater dispersion in Ce/Yb, perhaps representing a larger contribution of continental materials to the volcanics. Continental rift volcanics (CRV) are complex. The Antarctic rift data fall in the OIV field, and clearly define a hotspot origin for the rift with little contamination in the continental lithosphere, but most CRV data fall in the IAV field (Rio Grande rift tholeiites, Yellowstone Plateau basalts, Columbia River basalts, East African rift basalts). The Yellowstone basalt samples judged to be least crustally contaminated from other considerations (e.g., through Pb and Sr isotopes) approach closest to the OIV or hotspot field in the Ce/Yb vs. Ba/Ce plot, compatible with a hotspot origin with variable continental lithosphere interactions. The data from the Rio Grande rift have no such trend in Ce/Yb vs. Ba/Ce. Other trace element and isotopic data are suggestive of a different kind of origin, perhaps melting in the continental lithosphere from pressure release or other causes as suggested in the literature. Carbonatites, kimberlites, and ultrapotassic rocks form extreme end members for the peralkalic rocks on the continents with Ce/Yb values in the hundreds and even exceeding 1,000 in natrocarbonatite. Carbonatites and kimberlite type I, however, have Ba/Ce <8 with few exceptions. Ultrapo tassic rocks and kimberlite type II also have Ce/Yb values in the hundreds but with Ba/Ce >9. These rocks, although rare in the ocean basins (e.g., carbonatite on São Vicente Island in the Cape Verdes archipelago, Indian Ocean) plot similarly to their continental cousins. For Hawaii, the nephelinitic suites of both the Honolulu and Koloa series trend from alkali and alkali olivine basalt ratios toward higher signatures for Ce/Yb for other rock types. The Honolulu series, however, progresses towards smaller values of Ba/Ce for nephelinite-melilitite (Ce/Yb ˜ 85; Ba/Ce ˜ 5-7) near the low end of Ce/Yb found in carbonatite/kimberlite type I, whereas the Koloa series progresses toward higher Ba/Ce (Ce/Yb ˜ 65; Ba/Ce ˜ 14-15) for nephelinite-melilitite with Ce/Yb values near the lower end of kimberlite type II/ultrapotassic rocks. Carbonated phlogopitic sources have been proposed for peralkalic rocks of both oceans and continents. Carbonatites and/or kimberlites are suggested to possibly be present at depth under the Hawaiian nephelinitic series and in other OIV environments containing peralkalic suites.

International Geology Review

Geochemistry, geochronology, mineralogy, and geology suggest sources of and controls on mineral systems in the southern Toquima Range, Nye County, Nevada

Geochemistry maps showing the distribution and abundance of 18 elements in about 1,400 rock samples, both mineralized and unmineralized, from the southern Toquima Range, Nev., indicate major structural and lithologic controls on mineralization, and suggest sources of the elements. Radiometric age data, lead mineralogy and paragenesis data, and lead-isotope data supplement the geochemical and geologic data, providing further insight into timing, sources, and controls on mineralization. Major zones of mineralization are centered on structural margins of calderas and principal northwest-striking fault zones, as at Round Mountain, Manhattan, and Jefferson mining districts, and on intersections of low-angle and steep structures, as at Belmont mining district. Paleozoic sedimentary rocks, mostly limestones (at Manhattan, Jefferson, and Belmont districts), and porous Oligocene ash-flow tuffs (at Round Mountain district) host the major deposits, although all rock types have been mineralized as evidenced by numerous prospects throughout the area. Principal mineral systems are gold-silver at Round Mountain where about 7 million ounces of gold and more than 4 million ounces of silver has been produced; gold at Gold Hill in the west part of the Manhattan district where about a half million ounces of gold has been produced; gold-mercury-arsenic-antimony in the east (White Caps) part of the Manhattan district where a few hundred thousand ounces of gold has been produced; and silver-lead-antimony at Belmont where more than 150,000 ounces of silver has been produced. Lesser amounts of gold and silver have been produced from the Jefferson district and from scattered mines elsewhere in the southern Toquima Range. A small amount of tungsten was produced from mines in the granite of the Round Mountain pluton exposed east of Round Mountain, and small amounts of arsenic, antimony, and mercury have been produced elsewhere in the southern Toquima Range. All elements show unique distribution patterns that suggest specific sources and lithologic influences on deposition, as well as multiple episodes of mineralization. Principal episodes of mineralization are Late Cretaceous (molybdenum and tungsten in and near granite; silver at Belmont and Silver Point mines), early Oligocene [tourmaline and base- and precious-metals around the granodiorite of Dry Canyon stock as well as at Manhattan(?)], late Oligocene (gold at Round Mountain and Jefferson), and Miocene (gold at Manhattan). Most likely principal sources of molybdenum, tungsten, silver, and bismuth are Cretaceous granites; of antimony, arsenic, and mercury are intermediate-composition early Oligocene intrusives; and of gold are early and late Oligocene and early Miocene magmas of the volcanic cycle. Lead may have been derived principally from Cretaceous granitic magma and Paleozoic sedimentary rocks. Several areas prospective for undiscovered mineral deposits are suggested by spatial patterns of element distributions related to geologic features. The Manhattan district in the vicinity of the White Caps mine may be underlain by a copper-molybdenum porphyry system related to a buried stock; peripheral high-grade gold veins and skarn deposits may be present below deposits previously mined. The Jefferson district also may be underlain by a copper-molybdenum porphyry system related to a buried stock, it too with peripheral high-grade gold deposits. The Bald Mountain Canyon belt of small gold veins has potential for deeper deposits in buried porous ash-flow tuff similar to the huge Round Mountain low-grade gold-silver deposit. Several other areas have potential for a variety of mineral deposits. Altogether the geochemical, geochronologic, mineralogic, and geologic evidence suggests recurring mineralizing episodes of varied character, from Late Cretaceous to late Tertiary time, related to a long-lived hot spot deep in the crust or in the upper mantle. Granite plutons of Late Cretaceous age were minerali

Nevada

Wood River mining district, Idaho - intrusion-related lead-silver deposits derived from country rock source

Lead-silver deposits in the Wood River mining district occur in shear zones in hornfelsed argillite of the Devonian Milligen Formation near granitic plutons and under the Wood River thrust fault. The principal ore minerals are argentiferous galena and sphalerite; siderite is the principal gangue. The &delta; 34 S values of the sulfide minerals range from +2.2 to +15.0 permil, indicating that the sulfur had a shallow crustal source. &Delta; 34 S values between sphalerite and galena range from +2.3 to +3.4 permil, corresponding to sulfur isotope temperatures between 280&deg; and 182 &deg;C. Hydrothermal barite has a &delta; 34 S of +13.2 permil. Lead isotope ratios are radiogenic, also pointing to a shallow crustal source. Quartz gangue has &delta; 18 O of +16.4 permil and a calculated &delta; 18 O H20 at 270&deg;C of +8.4 permil. This value is reasonable for a hydrothermal fluid that had reached equilibrium with the argillite country rock. The siderite gangue has &delta; 18 O and &delta; 13 C values of +14.0 and -5.5 permil, respectively. Fluid inclusions have homogenization temperatures of 244&deg;-307&deg;C and average 270&deg;C. Freezing-stage measurements ranged from -1.85 to -2.8&deg;C, suggesting salinities of 3.2 to 4.8 weight percent. The &delta;D values of inclusion fluid in ore and gangue minerals are -110 to -120 permil. The geology, isotope, and fluid-inclusion data are consistent with a model of hydrothermal systems of meteoric water in faulted and shattered Paleozoic rocks near plutonic masses. This environment permitted deep circulation of the hydrothermal fluids, which dissolved the metals and sulfur from the Paleozoic host rocks and deposited ore in favorable beds or structures under the regional Wood River thrust fault.

Idaho

A list of references on lead isotope geochemistry, 1970-1974: (with an annendum to previous lead isotope listings)

This bibliography compiled primarily from Bibliography and Index of Geology, was constructed to be as complete as possible for final reports of studies that produced new data relative to geochemical application of: Common lead U-Th-Pb isotopic dating Pb-α Pb 210 , Pb 212 , Pb 214 No effort was made to include all: Annual reports, Yearbooks, etc. Review papers although many are included. Abstracts and theses were omitted.

Open-File Report

Variations in lead-isotopic compositions in Mesozoic granitic rocks of California: A preliminary investigation

Six alkali feldspar and two whole-rock samples of granitic rocks from the Sierra Nevada batholith and adjacent Klamath Mountains were analyzed for their lead-isotope compositions. The samples represented each of three 87 Sr/ 86 Sr groupings (< 0.704, 0.704 to 0.706, and > 0.706) for granitic rocks north of the Garlock fault in California. The isotopic compositions of lead in the samples from the Sierra Nevada batholith range from 18.73 to 19.37 for 206 Pb/ 204 Pb, 15.61 to 15.71 for 207 Pb/ 204 Pb, and 38.44 to 39.10 for 208 Pb/ 204 Pb. A crude parallel correspondence was found between lead and strontium isotopes, in that the specimens with the most radiogenic strontium also tend to have the most radiogenic lead similar to the previously studied Boulder batholith of Montana. A parallel correspondence is thought to imply characteristics of the source rocks for the plutons rather than consequences of partial melting or natural contamination. Lead-isotopic compositions for the Sierra Nevada batholith and the Boulder batholith differ, average values of 206 Pb/ 204 Pb being at least 18.8 for the Sierra Nevada batholith and about 18 for the Boulder batholith. In the Late Cretaceous part of the Sierra Nevada batholith, the secondary isochron “age” for the lead data in these rocks is about 2,900 m.y., far older than known Precambrian in California. Sources are proposed for these plutons from the lower continental crust and upper continental mantle or dominantly recycled continental materials, probably of intermediate composition and possibly carried down to the zone of melting by subduction. This source material may have been formed in Pre-cambrian times but did not undergo a Precambrian metamorphism greater than upper amphibolite facies which would have reduced the values of 238 U/ 204 Pb in the source rocks and resulted in Mesozoic leads like those found in the Boulder batholith and elsewhere in the Rocky Mountain region. A trondhjemite from the Klamath Mountains has a lead-isotope composition ( 206 Pb/ 204 Pb, 18.57; 207 Pb/ 204 Pb, 15.50; 208 Pb/ 204 Pb, 38.08) similar to that of oceanic volcanic rocks, particularly like those of island volcanics on oceanic ridges. Derivation of this trondhjemite from an oceanic mantle or recycled mantle material is indicated by this observation and supports the conclusion of Kistler and Peterman (1973) based on its alkali abundances and 87 Sr/ 86 Sr value.

California

U-Th-Pb chronology of zircons from the St. Kevin Granite, northern Sawatch Range, Colorado

Three samples of zircon from the St. Kevin Granite, northern Sawatch Range, Colorado, were analyzed for uranium, thorium, and lead content and for lead isotopic composition; the concentrated HNO 3 leaches of the zircons were similarly analyzed. The concordia age on the zircons was interpreted to be 1420 ± 40 m.y., an age in good agreement with a Rb-Sr whole-rock isochron age of 1470 m.y. (λ 87 Rb = 1.39 × 10 −11 yr −1 ). The concordia age of the leaches was found to be greater by about 5 percent than that of the zircons, perhaps reflecting loss of intermediate daughters in the 238 U decay chain over an extended period of time. Geologic evidence indicates that the St. Kevin Granite formed in large part by local melting of crustal rocks similar to the present wall rocks. If so, xenocrysts of zircon may be present in the granite. Isotopic evidence that the zircons were derived from older rocks is not convincing; however, possible evidence for a xenocrystic component is found in the feet that Pb-Pb ages of two nearly concordant zircons differ by 1.9 percent, an amount that exceeds analytical uncertainty. In addition, the zircon sample that has the greatest Pb-Pb age (1440 m.y.) has a 208 Pb/ 232 Th age of 1615 m.y. 208 Pb/ 232 Th ages greater than Pb-Pb ages are unusual and may suggest a complicated history for the sample. This sample is not the one suspected as the most likely to contain xenocrysts of zircon because xenoliths are not abundant at the sample locality. The zircons, if they are xenocrysts, apparently were almost entirely recrystallized or else lost nearly all their lead to the melt by diffusion.

Colorado

A list of references on lead isotope geochemistry through 1966

This bibliography was constructed to be as complete as possible for terminal papetrs containing new data relative to the geochmical applications of Common lead U-Th-Pb isotopic dating Pb-&alpha; Pb 210 , Pb 212 , Pb 214 No effort was made for completeness of: Annual report, Yearbooks, etc. Review papers although many are included. Abstract and these are omitted.

Open-File Report

Distribution and composition of sulfide minerals at Balmat, New York

In the Balmat area in northern New York , tabular deposits of sulfide minerals parallel the layering in folded, siliceous magnesian marbles of a metamorphic complex commonly referred to as the Precambrian Granville Series. Sphalerite, pyrite, and, locally, pyrrhotite and galena have replaced the carbonate minerals in parts of the marble units. The contacts between ore and marble are, in general, ill-defined; scattered grains of sulfides are present from several inches to hundreds of feet from the massive portions of ore. Access to the ore is provided through the Balmat No. 2 and No. 3 mines. The isotopic composition of lead from primary galena is uniform within an individual mine. The model age of this lead agrees with the age of the mineralization determined by other means - about a billion years. The isotopic composition of the leads in the marble is not uniform today, and calculations indicate that it was probably not uniform a billion years ago. Unless the lead in the ores is a uniform mixture of lead isotopes from an isotopically poorly mixed source, it is doubtful that the lead in the ores was derived from the surrounding marbles. Cobalt and nickel concentrations in pyrite from grains disseminated in the metasedimentary rocks away from the ore bodies are each greater than 200 ppm. Most samples of pyrite from the ore bodies at the No. 2 and No. 3 mines contain less than 50 ppm each of cobalt and nickel. Therefore the author believes it unlikely that the pyrite of the ores is genetically related to the pyrite in the metasedimentary rocks. Textural relationships suggest that pyrrhotite formed after most of the sphalerite, which in turn formed after most of the pyrite in the ore bodies. By use of the experimentally determined systems FeS-ZnS and FeS-FeS 2 , it is inferred from the amounts of iron in sphalerite and sulfur in pyrrhotite that the bulk of the sulfide minerals in the No. 2 mine formed above 320° C. The absolute temperature of formation of pyrrhotite indicated by the FeS-ZnS system is about 150° higher than that indicated by the FeS-FeS 2 system. The former system probably gives the more reliable estimate. The concentrations of individual minor elements in sphalerite and pyrite range considerably among specimens of the same sulfide mineral from the same level and ore body. An exception is cadmium in sphalerite which has a narrow concentration range around 1400 ppm in both the No. 2 and No. 3 mines. The ratio of the concentrations of minor elements between sphalerite-pyrite pairs varies considerably also. This variation probably indicates that exchange of minor elements between pyrite and sphalerite durin g the formation of the ores was very slow and incomplete.

New York