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Seabed minerals and the law of the sea

If, as seems likely, a comprehensive law-of-the-sea treaty is successfully concluded, minerals of the continental margins would be almost entirely controlled by coastal nations, and the right to produce minerals of the deep ocean floor would be licensed by an International Seabed Authority. Mineral production from the continental margins is likely to increase and diversify with time. The only minerals from the deep ocean floor for which there are reasonably good prospects of production within the next decade are the metalliferous muds from some of the deeps in the Red Sea (which lie within what is likely to be the jurisdiction of Saudi Arabia and Sudan) and nodules in the northeastern equatorial Pacific that contain recoverable metals, namely nickel, copper, cobalt, and possibly manganese, molybdenum, and vanadium.

Science↗

Mineral resources, environmental issues, and land use

Contrary to predictions from the 1950s through the mid-1980s, persistent shortages of nonfuel minerals have not occurred, despite prodigious consumption, and world reserves have increased. Global availability of raw materials is relevant to policy decisions regarding mineral development and land use. Justification for environmental protection may exceed that for mining a specific ore body. Demand for environmental accountability is rising worldwide, and new technologies are enabling internalization of costs. Mineral-rich developing nations plagued by inefficient state-owned mining enterprises, high population growth rates, and environmental degradation could realize substantial benefit by reforming government policies to encourage foreign investment in resources and by appropriate allocation of mineral rents.

Science↗

Mineral paragenesis of precambrian rocks in the Tenmile Range, Colorado

A Precambrian complex of granulite, gneiss, and migmatite, intruded by numerous plutons of granitic rocks correlated with the Silver Plume granite, is exposed in a long narrow belt along the crest and upper slopes of the Tenmile Range , Colorado . The metamorphic rocks are predominantly felsic; bands, lenses, and irregular bodies of mafic rocks rich in biotite, hornblende, and locally in sillimanite and garnet, are interlayered with the felsic rocks . The major lithologic variations in the metamorphic rock complex are believed to be due chiefly to variations in the original sedimentary rocks , which probably were interbedded sandstone, shale, and limestone. The metamorphic rocks and the Silver Plume granite reveal the age relations of quartz and the feldspars, and these relations afford considerable information on the origin and progressive transformation of the rocks . Quartz is the earliest mineral in the metamorphic rocks and is probably a relict mineral of a sandstone. It has been partially replaced by feldspar. It occurs chiefly in irregular clusters, some of which show sutured grains, enclosed in a ramifying network of feldspar. Irregular small apophyses, barbs, and prongs of feldspar penetrate the quartz clusters along grain boundaries and healed fractures in the quartz. In some of the least feldspathized quartzose metamorphic rocks the feldspar is clearly interstitial to the quartz. Quartz also occurs in feldspar as small spherical inclusions. The relations of the quartz to the feldspars show clearly that a quartzose host rock was replaced by feldspar along quartz grain boundaries, pre-existing healed fractures, and margins of shadowy areas in strained quartz grains. The textural relations of the other principal minerals in the metamorphic rocks show that plagioclase formed earlier than the microcline and that the micas were the last of the principal minerals to form. Identical paragenetic relations are found in the Silver Plume granite, and the writer concludes that the Silver Plume granite was derived by partial fusion of quartzose metamorphic rocks .

Colorado↗

O18/O16 ratios of coexisting minerals in glaucophane-bearing metamorphic rocks

Oxygen isotope analyses have been obtained for coexisting minerals in several blue-schist-facies metamorphic rocks from California, Oregon, and New Caledonia. Detailed isotopic studies were made on a continuous exposure of schist in Ward Creek, California, previously described by Coleman and Lee (1962). The oxygen isotope fractionations among coexisting minerals in a variety of rock types, including metasediments and metabasalts, are systematic and larger than those measured in pelitic schists metamorphosed at the grade of biotite zone or higher. Therefore, these Ward Creek rocks (termed Type III) must have formed at lower temperatures than have such pelitic schists. Evidence for significant isotopic equilibration and homogenization is observed in the Ward Creek sequence. Six different metasediments and metavolcanics collected within 25 m of one another show almost identical mineral δ; -values: quartz (15.8 to 16.3), aragonite (13.1 to 13.3), glaucophane (9.8 to 10.0), muscovite (10.9 to 11.3), lawsonite (9.3 to 9.5), and garnet (8.0 to 8.4), given as per mil enrichment in O 18 relative to mean ocean water. These rocks seem to have reached equilibrium at about the same temperature in contact with abundant metamorphic pore fluids. Not all the Ward Creek rocks have completely equilibrated with the postulated metamorphic pore fluids. In particular, the metacherts seem to have been relatively impermeable to the aqueous fluids during metamorphism, as indicated by the large δ -values of quartz in such rocks (17 to 19.2) and by their appreciably higher Fe +3 /Fe +2 ratios. Gradients in O 18 /O 16 and Fe +3 /Fe +2 have been generally “smoothed out” in the rocks during metamorphism, but the process has gone to completion only locally. Cherts and limestones have apparently been lowered in O 18 content by 10 to 15 per mil, and the metabasalts are enriched by 3 to 4 per mil over their unmetamorphosed parent rocks. Using the calibrated quartz-muscovite and quartz—CaCO 3 geothermometers, the measured quartz-muscovite and quartz-aragonite fractionations indicate essentially “concordant” temperatures of formation for the Type III rocks of 270° to 315° C. Inasmuch as aragonite is part of the equilibrium assemblage, these rocks must therefore have been metamorphosed at pressures of at least 6.4 to 7.0 kb. Oxygen isotope fractionations for the mineral pairs aragonite-lawsonite, quartz-muscovite, and quartz-glaucophane progressively decrease from Type II (low-grade) through Type III to Type IV (high-grade tectonic blocks) metabasalts. The higher-grade blueschists from New Caledonia exhibit quartz-muscovite and quartz-glaucophane fractionations similar to the Type IV metabasalts at Ward Creek, indicating temperatures of formation of 400° to 550° C. Thus, glaucophane-bearing metamorphic rocks apparently form over a temperature range of 200° C to 550° C, encompassing the probable temperature range of the entire greenschist and epidote-amphibolite facies. This suggests that glaucophane schists should be separated into at least two metamorphic facies, a lower-grade, lawsonite-aragonite blueschist facies and a higher-grade, epidote-rutile blueschist facies, both representing higher pressures than are attained during ordinary low-rank and middle-rank regional metamorphism.

California, Oregon↗

Oxygen-isotope exchange and mineral alteration in gabbros of the Lower Layered Series, Kap Edvard Holm Complex, East Greenland

Multiple intrusions of gabbros, mafic dikes, and syenites in the Kap Edvard Holm Complex gave rise to prolonged circulation of meteoric hydrothermal solutions and extreme isotope exchange and mineral alteration in the 3600-m-thick Lower Layered Series gabbros. In the Lower Layered Series, δ 18 O of plagioclase varies from +0.3‰ to -5.8‰, and it decreases with an increase in the volume of secondary talc, chlorite, and actinolite. In the same gabbros, pyroxenes have a more restricted range in δ 18 O, from 5.0‰ to 3.8‰ and values of δ 18 O pyroxene are independent of the abundance of secondary minerals, which ranges from 14% to 30%. These relations indicate that large amounts of water continued to flow through the rocks at temperatures of <500-600°C, altering the gabbros to assemblages of talc + chlorite + actinolite ± epidote ±albite and causing significant oxygen-isotope exchange in plagioclase, but not in pyroxene. The extensive low-temperature secondary mineralization and 18 O depletion of plagioclase in the Lower Layered Series are associated with the later emplacement of dikes and gabbros and syenites, which created new fracture systems and provided heat sources for hydrothermal fluid circulation. This produced subsolidus mineral alteration and isotope exchange in the Lower Layered Series that are distinct from those in the Skaergaard and Cuillin gabbros of the North Atlantic Tertiary province, but are similar to those observed in some oceanic gabbros.

Kap Edward Holm Complex↗

Geometry of the neoproterozoic and paleozoic rift margin of western Laurentia: Implications for mineral deposit settings

The U.S. and Canadian Cordilleran miogeocline evolved during several phases of Cryogenian-Devonian intracontinental rifting that formed the western mangin of Laurentia. Recent field and dating studies across central Idaho and northern Nevada result in identification of two segments of the rift margin. Resulting interpretations of rift geometry in the northern U.S. Cordillera are compatible with interpretations of northwest- striking asymmetric extensional segments subdivided by northeast-striking transform and transfer segments. The new interpretation permits integration of miogeoclinal segments along the length of the western North American Cordillera. For the U.S. Cordillera, miogeoclinal segments include the St. Mary-Moyie transform, eastern Washington- eastern Idaho upper-plate margin, Snake River transfer, Nevada-Utah lower-plate margin, and Mina transfer. The rift is orthogonal to most older basement domains, but the location of the transform-transfer zones suggests control of them by basement domain boundaries. The zigzag geometry of reentrants and promontories along the rift is paralleled by salients and recesses in younger thrust belts and by segmentation of younger extensional domains. Likewise, transform transfer zones localized subsequent transcurrent structures and igneous activity. Sediment-hosted mineral deposits trace the same zigzag geometry along the margin. Sedimentary exhalative (sedex) Zn-Pb-Ag ??Au and barite mineral deposits formed in continental-slope rocks during the Late Devonian-Mississippian and to a lesser degree, during the Cambrian-Early Ordovician. Such deposits formed during episodes of renewed extension along miogeoclinal segments. Carbonate-hosted Mississippi Valley- type (MVT) Zn-Pb deposits formed in structurally reactivated continental shelf rocks during the Late Devonian-Mississippian and Mesozoic due to reactivation of preexisting structures. The distribution and abundance of sedex and MVT deposits are controlled by the polarity and kinematics of the rift segment. Locally, discrete mineral belts parallel secondary structures such as rotated crustal blocks at depth that produced sedimentary subbasins and conduits for hydrothermal fluids. Where the miogeocline was overprinted by Mesozoic and Cenozoic deformation and magmatism, igneous rock-related mineral deposits are common. ??2008 Geological Society of America.

Geosphere↗

Mesozoic magmatism and timing of epigenetic Pb-Zn-Ag mineralization in the western Fortymile mining district, east-central Alaska: Zircon U-Pb geochronology, whole-rock geochemistry, and Pb isotopes

The Mesozoic magmatic history of the North American margin records the evolution from a more segmented assemblage of parautochthonous and allochthonous terranes to the more cohesive northern Cordilleran orogenic belt. We characterize the setting of magmatism, tectonism, and epigenetic mineralization in the western Fortymile mining district, east-central Alaska, where parautochthonous and allochthonous Paleozoic tectonic assemblages are juxtaposed, using sensitive high-resolution ion microprobe (SHRIMP) U-Pb zircon geochronology, whole-rock geochemistry, and feldspar Pb isotopes of Mesozoic intrusions and spatially associated mineral prospects. New SHRIMP U-Pb zircon ages and published U-Pb and 40 Ar/ 39 Ar ages indicate four episodes of plutonism in the western Fortymile district: Late Triassic (216-208 Ma), Early Jurassic (199-181 Ma), mid-Cretaceous (112-94 Ma), and Late Cretaceous (70-66 Ma). All age groups have calc-alkalic arc compositions that became more evolved through time. Pb isotope compositions of feldspars from Late Triassic, Early Jurassic, and Late Cretaceous igneous rocks similarly became more radiogenic with time and are consistent with the magmas being mantle derived but extensively contaminated by upper crustal components with evolving Pb isotopic compositions. Feldspar Pb isotopes from mid-Cretaceous rocks have isotopic ratios that indicate magma derivation from upper crustal sources, probably thickened mid-Paleozoic basement. The origin of the mantle component in Late Cretaceous granitoids suggested by Pb isotopic ratios is uncertain, but we propose that it reflects asthenospheric upwelling following slab breakoff and sinking of an inactive inner subduction zone that delivered the previously accreted Wrangellia composite terrane to the North American continental margin, after the outer Farallon subduction zone was established. Epigenetic Pb-Zn-Ag &plusmn; Cu prospects in the western Fortymile district are spatially associated with splays of the northeast-trending Kechumstuk sinistral-normal fault zone and with ca. 68-66 Ma felsic intrusions and dikes. The similarity between Pb isotope compositions of feldspars from the Late Cretaceous igneous bodies and sulfides from the epithermal prospects suggests a Late Cretaceous age for most of the mineralization. Fluid flow along the faults undoubtedly played a major role in mineralization. We interpret displacement on the northeast-trending faults to be a far-field effect of dextral translation along Late Cretaceous plate-scale boundaries and faults that were roughly parallel to the subsequently developed Denali and Tintina fault systems, which currently bound the region.

Alaska↗

Mineral layering in the Twin Lakes granodiorite, Colorado

The Twin Lakes intrusion is composed mainly of coarse-grained porphyritic granodiorite, and is zoned from a felsic core to a slightly more mafic border. Steeply dipping mineral layers, typically a few inches to 5 feet thick and several tens of feet long, occur in discontinuous marginal zones as wide as 5000 feet. Four main types of layers are defined by increased abundances of orthoclase, quartz, plagioclase, and mafic minerals. The characteristic minerals of each type of layer differ markedly in size (orthoclase, average length about 10 cm; quartz, average diameter about 1 cm; plagioclase, average length .45 mm; and mafic minerals, average length .15 mm). Textural evidence from fine-grained granodiorite porphyry and deformed mafic layers indicates that the magma contained 50 to 60 volume percent suspended crystals during emplacement. Structures in the mafic layers such as size and concentration grading normal to the plane of layering, wedge layering, and cross layering superficially resemble sedimentary structures. Inspection of these structures, however, reveals a number of features that are difficult to explain by a process of sedimentation, but which are consistent with a flow sorting process accompanied by deformation. The layering probably formed by size sorting of the suspended crystals in marginal zones of the intrusion by essentially vertical shear flow during emplacement.

Colorado↗

Clay minerals: A guide to their x-ray identification

This paper is a guide to the X-ray examination of clay minerals; it incorporates background information concerning the principal crystallographic features of clay minerals, and how this is used in the X-ray identification of these minerals, together with laboratory techniques and the application of X-ray diffractometry to the diagnosis of the clay minerals in natural sedimentary materials.

Special Papers of the Geological Society of Americ↗

Paleomagnetic and mineral magnetic constraints on Zn-Pb ore genesis in the Pend Oreille Mine, Metaline district, Washington, USA

Zinc-lead mineralization in the Metaline mining district of northeastern Washington, USA, is hosted by the Cambrian Metaline Formation and is classified into Yellowhead-type (YO) and Josephine-type (JO) ore based on texture and mineralogy. Paleomagnetic results are reported for four Cambrian Metaline Formation sites, one Ordovician Ledbetter slate site, 12 YO and 13 JO (including two breccia sites) mineralization sites in the Pend Oreille Mine, and eight sites from the nearby Cretaceous Kaniksu granite batholith. Thermal and alternating field step demagnetization, saturation isothermal remanence analysis, and synthetic specimen tests show that the remanence in the host carbonates and Zn-Pb mineralization is carried mostly by pseudosingle (PSD) to single domain (SD) pyrrhotite and mostly by PSD to SD magnetite in the Kaniksu granite. Based on thermomagnetic measurements, sphalerite and galena concentrates and tailings from the mine's mill contain hexagonal and monoclimc pyrrhotite. The postfolding characteristic remanent magnetization (ChRM), known thermal data, and paleoarc method of dating suggest that the Zn-Pb mineralization carries a primary chemical remanent magnetization (CRM), and Metaline Formation carbonates a secondary CRM that were acquired during the Middle Jurassic (166 ??6 Ma) during the waning stages of the Nevadan orogeny. A paleomagnetic breccia test favours a solution-collapse origin for the Josephine breccia. Finally, the Kaniksu paleopole is concordant with the North American Cretaceous reference paleopole, suggesting the Kootenay terrane has not been rotated since emplacement of the batholith at ???94 Ma. ?? 2007 NRC Canada.

Canadian Journal of Earth Sciences↗

Natural calcium isotonic composition of urine as a marker of bone mineral balance

Background: We investigated whether changes in the natural isotopic composition of calcium in human urine track changes in net bone mineral balance, as predicted by a model of calcium isotopic behavior in vertebrates. If so, isotopic analysis of natural urine or blood calcium could be used to monitor short-term changes in bone mineral balance that cannot be detected with other techniques. Methods: Calcium isotopic compositions are expressed as ??44Ca, or the difference in parts per thousand between the 44Ca/40Ca of a sample and the 44Ca/ 40Ca of a standard reference material. ??44Ca was measured in urine samples from 10 persons who participated in a study of the effectiveness of countermeasures to bone loss in spaceflight, in which 17 weeks of bed rest was used to induce bone loss. Study participants were assigned to 1 of 3 treatment groups: controls received no treatment, one treatment group received alendronate, and another group performed resistive exercise. Measurements were made on urine samples collected before, at 2 or 3 points during, and after bed rest. Results: Urine ??44Ca values during bed rest were lower in controls than in individuals treated with alendronate (P <0.05, ANOVA) or exercise (P <0.05), and lower than the control group baseline (P <0.05, Mest). Results were consistent with the model and with biochemical and bone mineral density data. Conclusion: Results confirm the predicted relationship between bone mineral balance and calcium isotopes, suggesting that calcium isotopic analysis of urine might be refined into a clinical and research tool. ?? 2007 American Association for Clinical Chemistry.

Clinical Chemistry↗

Book review: Mineral resource estimation

Mineral Resource Estimation is about estimating mineral resources at the scale of an ore deposit and is not to be mistaken with mineral resource assessment, which is undertaken at a significantly broader scale, even if similar data and geospatial/geostatistical methods are used. The book describes geological, statistical, and geostatistical tools and methodologies used in resource estimation and modeling, and presents case studies for illustration. The target audience is the expert, which includes professional mining geologists and engineers, as well as graduate-level and advanced undergraduate students. Review info: Mineral Resource Estimation . By Mario E. Rossi, Clayton V. Deutsch . 2014 . ISBN 978-1-4020-5716-8 332 pp.

Economic Geology↗

Nevadaite, (Cu2+, Al, V3+)6 [Al8 (PO4)8 F8] (OH 2 (H2O)22, a new phosphate mineral species from the Gold Quarry mine, Carlin, Eureka County, Nevada: Description and crystal structure

Nevadaite, (Cu 2+ , □, Al, V 3+ ) 6 (PO 4 ) 8 F 8 (OH) 2 (H 2 O) 22 , is a new supergene mineral species from the Gold Quarry mine, near Carlin, Eureka County, Nevada, U.S.A. Nevadaite forms radiating clusters to 1 mm of prismatic crystals, locally covering surfaces more that 2 cm across; individual crystals are elongate on [001] with a length:width ratio of > 10:1 and a maximum diameter of ~30 μm . It also occurs as spherules and druses associated with colorless to purple-black fluellite, colorless wavellite, strengitevariscite, acicular maroon-to-red hewettite, and rare anatase, kazakhstanite, tinticite, leucophosphite, torbernite and tyuyamunite. Nevadaite is pale green to turquoise blue with a pale powder-blue streak and a vitreous luster; it does not fluoresce under ultra-violet light. It has no cleavage, a Mohs hardness of ~3, is brittle with a conchoidal fracture, and has measured and calculated densities of 2.54 and 2.55 g/cm 3 , respectively. Nevadaite is biaxial negative, with 1.540, β 1.548, γ 1.553, 2 V (obs.) = 76°, 2 V (calc.) = 76° , pleochroic with X pale greenish blue, Y very pale greenish blue, Z blue, and with absorption Z ≫ X > Y and orientation X = c, Y = a, Z = b. Nevadaite is orthorhombic, space group P 2 1 mn , a 12.123(2), b 18.999(2), c 4.961(1) Å, V 1142.8(2) Å 3 , Z = 1, a:b:c = 0.6391:1:0.2611 . The strongest seven lines in the X-ray powder-diffraction pattern [ d in Å(I)( hkl )] are: 6.077(10)(200), 5.618(9)(130), 9.535(8)(020), 2.983(6)(241), 3.430(4)(041), 2.661(4)(061), and 1.844(4)(352). A chemical analysis with an electron microprobe gave P 2 O 5 32.54, Al 2 O 3 27.07, V 2 O 3 4.24, Fe 2 O 3 0.07, CuO 9.24, ZnO 0.11, F 9.22, H 2 O (calc.) 23.48, OH ≡ F–3.88, sum 102.09 wt.% ; the valence states of V and Fe, and the amount of H 2 O , were determined by crystal-structure analysis. The resulting empirical formula on the basis of 63.65 anions ( including 21.65 H 2 O pfu ) is ( (Cu 2.00 2+ Zn 0.02 V 0.98 3+ Fe 0.01 3+ Al 1.15 ) ∑ 4.16 Al 8 P 7.90 O 32 [F 8.37 (OH) 1.63 ] ∑10 (H 2 O) 21.65 . The crystal structure of nevadaite was solved by direct methods and refined to an R index of 4.0% based on 1307 observed reflections collected on a four-circle diffractometer with Mo K α X-radiation . The structure consists of ordered layers of vertex-sharing octahedra and tetrahedra alternating with layers of disordered vertex-sharing and face-sharing octahedra in the b direction. [Alϕ 5 ] chains of octahedra are decorated by (PO 4 ) tetrahedra that share vertices with octahedra adjacent in the chain . These chains link in the c direction by sharing vertices between octahedra and tetrahedra to form an ordered layer of the form [Al 8 (PO 4 ) 8 F 8 (H 2 O) 8 ] . In the disordered layer, octahedra containing positionally disordered Cu 2+ , V 3+ , Al and □ (vacancy) share trans faces to form columns that link by sharing octahedron vertices to form ribbons extending in the c direction; the resulting layer has the form {(Cu 2 2+ □ 2 V 3+ ,Al) ∑6 (H 2 O) 12 (OH) 2 (H 2 O) x }, x ≈ 2 . The layers link in the b direction by sharing vertices between octahedra and tetrahedra. Although decorated chains topologically equivalent to that in nevadaite are common in many oxysalt minerals, its chain is geometrically distinct from those topologically equivalent chains. The M – M linkage along the [ M ϕ 5 ] chains in most minerals take place through trans vertices of the octahedra, with one example of linkage through cis vertices; in nevadaite, the M – M linkage involves both trans and cis vertices, as does the chain in slavíkite . In most of these decorated chains, alternate tetrahedra along the chain occur either in a trans or a cis arrangement. In nevadaite and slavíkite, the tetrahedra are arranged in both trans and cis arrangements; the arrangements in these two minerals are geometrically distinct, however.

Nevada↗

The manganese oxide minerals, a preliminary report

This paper summarizes the results obtained thus far in an intensive study of the manganese oxide minerals. X-ray powder photographs, supplemented by chemical tests, have proved to be the best means for identifying these minerals. Formulas are suggested. Physical properties and X-ray data are listed for the commoner minerals and those for which new data have been obtained. Rules of nomenclature for these minerals are suggested.

Economic Geology↗

Direct dating of mineralization at Goldfield, Nevada, by potassium-argon and fission-track methods

Potassium-argon dating of hypogene alunite and K-mica from hydrothermally altered rocks at Goldfield, Nevada, yields mineralization ages of 20 to 21 m.y., in good agreement with a mineralization age established by potassium-argon dating of unaltered premineralization and postmineralization volcanic units. Premineralization volcanic units that are pervasively propylitized cannot be dated by the potassium-argon method but yield zircon fission-track ages, and in several cases yield concordant apatite fission-track ages. Two samples from premineralization units yield apatite ages concordant with the age of mineralization established by potassium-argon geochronometry, reflecting annealing of the apatite during the hydrothermal episode.Potassium-argon dating of supergene alunite samples yields imprecise ages in the range 9 to 12 m.y. that probably record the first exposure of their hydrothermally altered host rocks to oxidizing conditions. Potassium-argon dating of postmineralization basalts and silicic tuffs interbedded with conglomerates bearing altered rock clasts shows that the altered area was eroded nearly to present topographic levels by 11 m.y. ago, at which time it was covered by basalt flows now represented only by scattered remnants. Apatites from premineralization volcanic units give fission-track ages of 20 m.y. or more, indicating that no significant thermal event has affected altered rocks at Goldfield since mineralization took place.

Nevada↗

Origin of a South Texas roll-type uranium deposit; I, Alteration of iron-titanium oxide minerals

The detrital Fe-Ti oxide minerals and their authigenic alteration products in samples from cores spanning 1.7 km across a roll-type uranium deposit in the mid-Tertiary Catahoula Tuff, south Texas, record important information on host-rock preparation and on development of the altered tongue of the deposit. In reduced rock, in front of and enveloping the altered tongue, iron disulfide minerals (pyrite and marcasite) have partially to completely replaced titanomagnetite and, to a lesser extent, titanohematite. Subsequent oxidation of these sulfidized Fe-Ti oxides, by processes that formed the altered tongue and uranium roll, produced ferric oxide and hydroxide phases (limonite) pseudomorphous after the sulfides. Fe-Ti oxides 1.0 km updip from the roll front were never sulfidized; titanomagnetite (partly replaced by hematite) and martite constitute nearly half of the heavy mineral fraction and limonite is absent. Oxidized rocks 210 m and closer to the nose of the roll front, however, are nearly devoid of titanomagnetite and contain abundant limonite. The redox interface that bounds the altered tongue, therefore, moved more than 210 m but less than 1.0 km. Detrital Fe-Ti oxide minerals are increasingly sulfidized in the downdip direction indicating that initial sulfidizaton was more intense in that direction. Organic carbon content is uniformly very low throughout the host sandstone, which implies that heterotrophic sulfate-reducing bacteria were not involved in the generation of sulfide. The H 2 S for the initial sulfidization may have been derived from oil and gas in formations that underlie the Catahoula Tuff. The H 2 S probably invaded the Catahoula along a fault that is 1.5 km downdip from the present roll front.

Texas↗

The Schwarzwalder uranium deposit, III: Alteration, vein mineralization, light stable isotopes, and genesis of the deposit

The Schwartzwalder uranium deposit formed at 69.3 + or - 1.1 m.y. in a complex fracture system during the inception of Laramide uplift of the Front Range in Colorado. Geologic and isotopic evidence demonstrates that the ore-forming fluids were in chemical equilibrium with the Proterozoic metavolcanic and metasedimentary host-rock terrane at depth and that the metals, sulfur, and carbonate deposited in the fractures were derived from the metamorphic rocks. The data are not consistent with chemical contributions from an unrecognized magma or from the overlying Phanerozoic sedimentary rocks. The protoliths for the metamorphic rocks were submarine volcanic rocks and related volcanogenic exhalative iron-formations and chert. Water trapped along the basement faults and in the regolith between the basement and the overlying Paleozoic sedimentary rocks interacted with the metavolcanic rocks to produce isotopically heavy fluids containing high concentrations of dissolved metals and carbonate. Calculated delta 18 O values for this fluid range from 4.3 to 8.2 per mil, indicating a low water/rock ratio in the source terrane.Two stages of alteration and three stages of vein mineralization are recorded in the Schwartzwalder deposit. At the onset of Laramide faulting, fluids migrated along the fracture systems to zones of low hydraulic potential. These fluids contained CO 2 and had a metastably large K/Na ratio; they altered the gneissic wall rocks to a carbonate-sericite assemblage, adding K (super +) and CO 2 and removing SiO 2 with little or no change in volume. As the fractures continued to open, CO 2 was evolved from the fluids, increasing the pH and superimposing a hematite-adularia alteration assemblage on the earlier alteration.The veins record three stages of mineralization, the second of which generated the high-grade uranium veins. Evidence for the stage I sulfide-carbonate mineralization is poorly preserved, but isotopic and temperature data from this stage are consistent with a trend in fluid composition culminating in stage II pitchblende deposition. Sudden, large movements along the faults caused episodic evolution of CO 2 from the fluid. This loss of CO 2 decreased the solubilities of carbonates and adularia and the stabilities of sulfur species in solution. Uranyl carbonate complexes dissociated and sulfur species in solution likely reduced the uranyl ions to produce stage II pitchblende. Carbonate, adularia, and sulfides dominated the vein mineralogy after deposition of pitchblende. Progressively lower delta 18 O values in vein carbonates suggest the mixing of cooler, less evolved, perhaps meteoric, waters during the later stages of mineralization. However, the fluid pressure remained high, as indicated by explosion breccias and inward collapse features which formed as fault movements produced sudden decreases in the confining pressure. Only the stage III carbonate-iron disulfide assemblage in the major postore segment of the Illinois fault may be the product of meteoric water alone.

Economic Geology↗

Geophysical and isotopic constraints on crustal structure related to mineral trends in north-central Nevada and implications for tectonic history

We combined information from Sr and Pb isotope data and magnetotelluric models to develop a new magnetic and gravity interpretation of the crustal structure of north - central Nevada to better understand the origin of mineral trends . The new interpretation suggests a crustal structure that is composed of Precambrian continental crust, transitional crust, and primarily oceanic crust that are separated by northwest- and northeast-striking fault zones. The magnetic expression of the buried Precambrian continental crust is recognized for the first time. Low magnetic values primarily reflect magnetite-poor crystalline crust rather than elevated temperatures at depth. Northwest- and northeast-striking crustal boundaries are defined by isotopic data and abrupt gradients in gravity and magnetic data. The Carlin and Battle Mountain-Eureka mineral trends are associated with two of three northwest-striking boundaries. The Carlin boundary is primarily defined by a change in density and isotopic character of the lower to middle crust. The Battle Mountain-Eureka boundary coincides with a density contrast in the upper crust and a change in isotopic character in the lower to middle crust. Magnetotelluric models suggest that the Battle Mountain-Eureka boundary represents a crustal fault zone for most of its extent, but that deep-rooted faulting is more complex near and northwest of Battle Mountain. Crustal fault zones inferred from the magnetotelluric models near the Carlin trend are oblique to it, suggesting that they may not have been controlled by the deep boundary seen in the gravity and isotopic data. The third northwest-trending boundary is related to the western edge of the buried Precambrian continent in west- central Nevada , but lacks an associated mineral trend . A northeast-striking boundary forms the northern limit of Precambrian continental and transitional crust. The boundaries may have originated as rift or transform faults during Precambrian breakup of Rodinia or as faults accommodating lateral movements or accretion during later Paleozoic tectonic events. Comparing the crustal structure to tectonic elements produced by successively younger events shows that it had a profound influence on subsequent sedimentation, deformation, magmatism, extension, and most important, mineralization.

Nevada↗