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R. G. Coleman

Publications and source records attributed to R. G. Coleman.

25 records · Page 2Linked to original sources

Glaucophane-bearing metamorphic rock types of the Cazadero area, California

A detailed field and laboratory study has been made of a well-exposed glaucophane schist sequence within the Jurassic and Cretaceous Franciscan Formation of northern California. Three types of glaucophane-bearing metamorphic rocks have been distinguished in and around the area of the detailed study. Each is characterized by distinctive textures and mineral assemblages that are interpreted to represent different grades of metamorphism within the glaucophane schist facies. From the combination of small- and large-scale mapping in the area described it is clear that coarsely schistose blocks, tens of feet in diameter, commonly rest directly upon and within less intensely metamorphosed terrain. In the Cazadero area these isolated blocks of coarsely crystalline rocks are concentrated in a band that is roughly concordant with some of the major faulting, and their metamorphic fabric shows no consistent relation to local or regional structures. It is tentatively suggested that these blocks have been transported upward tectonically and that they are not stratigraphically equivalent to the other types of glaucophane-bearing metamorphic rocks in the area. Chemical and petrographic evidence indicates that basalt and sediments have been converted to glaucophane-bearing rocks under conditions of metamorphism that were essentially isochemical, except for fugitive components and some minor elements.

California

Temperature of crystallization of pyrrhotite and sphalerite from the Highland-Surprise Mine, Coeur d'Alene district, Idaho

The ore bodies of the Highland-Surprise Mine are replacements along shear zones in quartzose slate, quartzite, and phyllite of the Prichard Formation of the Belt series (Precambrian). Pyrite, arsenopyrite, pyrrhotite, sphalerite, chalcopyrite, and galena are the chief metallic minerals and were probably deposited in that order. Temperatures of formation were estimated for pyrrhotite-pyrite and sphalerite-pyrrhotite assemblages contained in the steeply dipping vein system. Measurements on 62 pyrrhotites indicate a range in temperature of crystallization between 370 degrees and 492 degrees C. (no correction required for confining pressures <2000 bars below 670 degrees C.), and measurements on 14 sphalerites indicate crystallization temperatures between 375 degrees and 460 degrees C. (uncorrected for confining pressure). No systematic temperature gradients were recognized. Minor elements in 23 pyrrhotite, 8 pyrite, 13 sphalerite, and 2 galena samples were determined. Partition ratios of Ni and Co in pyrrhotite-pyrite and sphalerite-pyrrhotite pairs are erratic. This suggests a dis-equilibrium distribution of these elements between the phases of each mineral pair and/or b) crystallization of the mineral pairs under different physical conditions.

Idaho

Jadeite deposits of the clear creek area, New Idria district, San Benito county, California

Tectonic inclusions within the New Idria serpentine body contain jadeite in two distinct assemblages: (1) Lenslike inclusions containing a monomineralic green jadeite core surrounded by a calc-silicate rim. (2) Jadeite veins cross-cutting albite-crossite schist inclusions. In these veins jadeite coexists with low albite; green jadeite (Jd 75 Ac+Di+He 25) coexists with low albite within the host schist. Albite schists are related to the pre-metamorphic keratophyres and it can be shown that desilication of such rocks produces a bulk composition similar to that of jadeite. Metamor-phism of keratophyric tectonic inclusions within serpentine produced jadeite-albite schists along margins of the inclusions. Jadeite-albite veins formed from mobilized liquids rich in the jadeite molecule and deficient in water. Geological evidence such as would indicate extreme pressures or temperatures during jadeite formation is lacking; rather, a low silica and dry system allowed its formation at reduced temperatures and pressures.

California

New occurrences of ferroselite (FeSe2)

Iron selenide from the uranium-vanadium ores of the Colorado Plateau was under investigation when ferroselite was described as a new mineral in Russia by Bur'yanova and Komkov (1955). Association of ferroselite with selenian pyrite and marcasite within discrete areas of these uranium-vanadium deposits suggests an unusual environment of formation. Its association with apparent low temperature assemblages in the United States and Bussia indicates that its minimum temperature of formation is quite low. Chemical analyses of ferroselite agree well with the theoretical formula FeSe 2 ; material from the Virgin no. 3 mine, Montrose County, Colorado, gives the formula FeSe 2.07 and that from the A.E.C. no. 8 mine, Temple Mountain, Utah, gives the formula (Fe, Co)Se 2.08 . The similarity of hastite and ferroselite suggests that a complete series FeSe 2 -CoSe 2 may exist. In contrast to this, pyrite associated with ferroselite apparently will camouflage only 4 per cent (molecular) FeSe 2 within its structure. Ferroselite cannot be distinguished from rammelsbergite (FeAs 2 ) by X-ray or in polished section; therefore, the exact identification of these two minerals can be made only by specific tests for As or Se. As hastite (CoSe 2 ) and marcasite are in the same structure group as ferroselite and rammelsbergite, identification of these minerals should include qualitative chemical determinations.

Geochimica et Cosmochimica Acta

Occurrence of selenium in sulfides from some sedimentary rocks of the western United States

Investigations of the minor- and trace-element content of sulfides associated with uranium ore deposits from sandstone-type deposits have shown that selenium commonly substitutes for sulfur. The Morrison formation and Entrada sandstone of Jurassic age and the Wind River formation of Eocene age seem to be seleniferous stratigraphic zones; sulfides deposited within these formations generally contain abnormal amounts of selenium. The selenium content of the pyrite, marcasite, and chalcocite is much greater than that reported in previously published data.Under the prevailing temperatures and pressures of formation of the Colorado Plateau uranium deposits the maximum amount of Se substituting for S in the pyrite structure was found to be 3 percent by weight. Ferroselite, the iron selenide (FeSe 2 ), was found in two deposits on the Colorado Plateau and it was also established that galena (PbS) forms an isomorphous series with clausthalite (PbSe) in nature.During oxidation of the selenium-bearing sulfides and selenides from the Colorado Plateau and Wyoming, the selenium forms pinkish crusts of either monoclinic or hexagonal native selenium intergrown with soluble sulfates, suggesting that under "normal" oxidizing conditions native selenium is more stable than selenites or selenates. The above-normal selenium content of these sulfides from sedimentary rocks of Mesozoic and Tertiary age is significant. The high selenium in these sulfides is related to periods of volcanic and intrusive activity penecontemporaneous with the formation of the containing sediments.

Arizona, Colorado, New Mexico, Utah, Wyoming

Detailed mineral and chemical relations in two uranium-vanadium ores

Channel samples from two mines on the Colorado Plateau have been studied in detail both mineralogically and chemically. A channel sample from the Mineral Joe No. 1 mine, Montrose County, Colo., extends from unmineralized rock on one side, through a zone of variable mineralization, into only weakly mineralized rock. The unmineralized rock is a fairly clean quartz sand cemented with gypsum and contains only minor amounts of clay minerals. One boundary between unmineralized and mineralized rock is quite sharo and is nearly at right angles to the bedding. Vanadium clay minerals, chiefly mixed layered mica-montmorillonite and chlorite-monmorillonite, are abundant throughout the mineralized zone. Except in the dark "eye" of the channel sample, the vanadium clay minerals are accompanied by hewettite, carnotite, tyuyamunite, and probably unidentified vanadates. In the dark "eye," paramontroseite, pyrite, and marcasite are abundant, and bordered on each side by a zone containing abundant corvusite. No recognizable uranium minerals were seen in the paramontroseite zone although uranium is abundant there. Coaly material is recognizable throughout all of the channel but is most abundant in and near the dark "eye." Detailed chemical studies show a general increase in Fe, Al, U, and V, and a decrease in SO 4 toward the "eye" of the channel. Reducing capacity studies indicate that V(IV) and Fe(II) are present in the clay mineral throughout the channel, but only in and near the "eye" are other V(IV) minerals present (paramontroseite and corvusite). The uranium is sexivalent, although its state of combination is conjectural where it is associated with paramontroseite. Where the ore boundary is sharp, the boundary of introduced trace elements is equally sharp. Textural and chemical relations leave no doubt that the "eye: is a partially oxidized remnant of a former lower-valence ore, and the remainder of the channel is a much more fully oxidized remnant. A channel sample from the Virgin No. 3 mine, Montrose County, Colo., extends from weakly mineralized sandstone on both sides through a strongly mineralized central zone. The weakly mineralized zone is a poorly sorted sandstone with common detrital clay partings; chlorite and mixed layer mica-montmorrillonite are abundant interstitial to the quartz grains. No distinct vanadium or uranium minerals are recognizable, although the clay minerals are vanadium bearing. Euherdral pyrite grains and selenian galena are present but rare. The strongly mineralized rock is separated from the weakly mineralized rock by a narrow transition zone which only apporiximates the bedding planes. It contains abundant vanadium-bearing clay minerals (predominantly chlorite) interstitial to the quartz grains, and apparently replacing them. Paramontroseite is common and is intergrown with the clay minerals. Pyrite and marcasite are present, chiefly in or near the abundant blebs and fragments of carbonaceous material. Selenian galena is rarely present, and generally in or near carbonaceous material. Coffinite is the only uranium mineral idenitified; it is extremely fine grained and was identified only in X-ray diffraction patterns of heavy separates. Distribution of trace elements is not clear; some are consistently high in the strongly mineralized rocks, and some are consistently low. The trace element composition of the unmineralized rock is not known. Chemical studies show a very abrupt rise in the total U, V, and Fe from the weakly mineralized to strongly mineralized rock. Reducing-capacity studies indicate that most of the vanadium is present as V(IV), but some is present as V(V); that iron is present as both Fe(II) and Fe(III), the latter believed to have been present in the primary clays of the unmineralized rock; and that come of the uranium is present as U(VI) in addition to the U(IV) in the coffinite. All evidence points to weak oxidation of an ore once having a somewhat lower valence state. The channel samples from both the Mineral Joe No. 1 mine and the Virgin No. 3 mine are believe to have been essentially identical in mineralogy prior to oxidation by weathering: vanadium was present as V(III) in montroseite and V(IV) in the vanadium clays; uranium was present largely as U(IV) in coffinite and/or uraninite. The Mineral Joe No. 1 mine channel sample is now more fully oxidized. Vanadium clays are unquestionably formed abundantly during the primary mineralization, and they persist with a minimum of alteration during much of the weathering. They suggest that the vanadium is carried as V(IV) in the ore-forming fluids; it seems likely too that the uranium is carried as a U(VI) ion.

Trace Elements Investigations

Garnet types from the Cazadero area, California

This is the third in a series of papers on glaucophane schists from the Franciscan Formation near Cazadero, California. Previous papers describe three distinct types of glaucophane-bearing Franciscan metamorphic rocks near Cazadero. The purpose of this study is to investigate the garnets present in metamorphic types III (bedrock schists) and IV (tectonic blocks) as defined by Coleman & Lee (1963). Twenty-four garnet analyses are presented. Sixteen of these are from (aragonite-bearing) type III glaucophane schists, and eight are from type IV glaucophane schists. Type IV rocks include California eclogites. Type III rocks include metabasalt, metachert, metashale, meta-ironstone, and metacarbonate that were formed under high pressure and relatively low temperature. These rocks contain garnets that display a wide range of composition, but the dominant molecules represented are consistently almandine, spessartine, and grossular. Type IV rocks are mainly metabasalts that were probably formed under higher temperatures and pressures than type III rocks. There is a distinct difference between garnets from type III rocks and those from type IV (including eclogites); the lattercontain less spessartine and more pyrope, and the dominant molecules are almandine and grossular. The four analyses of garnets from California eclogites have an average pyrope content of about ten molecular per cent, and they extend the range of composition reported for eclogite garnets. Quantitative spectrographic determinations of minor elements are listed for each of the garnets described. The values determined for some of the minor elements have a wide range and a capricious distribution over a few feet of outcrop area. As a group, both the garnets from type III rocks and those from type IV are pyralspites with large contents (as much as 35 molecular per cent) of ugrandite. This unusual admixture of the pyralspite and ugrandite garnet series may have resulted in part from the conditions (high pressures and relatively low temperatures) under which the enclosing rocks were recrystallized.

California