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At least 1,315 records · Page 73Linked to original sources

USGS1972

Geology and mineral deposits of the Hekimhan-Hasancelebi iron district, Turkey

An area of 210 sq km was investigated in the Hekimhan-Hasancelebi district. of central Turkey as part of the Maden Tetkik ve Arama Institusu(MTA)-U. S. Geological Survey(USGS) mineral exploration and training project to explore for iron deposits and to provide on-.the-job training for MTA geologists. The rocks of the area are Cretaceous and Tertiary sedimentary and volcanic rocks intruded by syenite and a serpentinized mafic and ultramafic complex and overlain unconformably by late .Tertiary basalt. The base of the section is a thick mafic volcanic-sedimentary sequence with diverse rocks that include conglomerate, sandstone, shale, tuff, limestone, and basalt. The upper part of the sequence is metasomatized near syenite contacts. The sequence is conformably overlain by trachyte and unconformably overlain by massive limestone. Overlying the limestone is a Tertiary sedimentary sequence which is dominantly conglomerate and sandstone with local limestone and volcanic rocks. This series is in turn overlain by olivine basalt. Mineral deposits are associated with the two types of intrusive rocks. Hematite-magnetite in the Karakuz mine area and in the Bahcedami-Hasancelebi area is related to the syenite, and siderite in the Deveci mine area is possibly related to the mafic-ultramafic rocks. Significant iron resources are found, only in the Karakuz and Deveci areas. In the Karakuz area disseminations, veins, and replacements consisting of hematite and magnetite are present. Most of the material is low grade. In the Deveci mine area a large deposit of siderite apparently is a replacement of carbonate beds adjacent to serpentinized igneous rock. The upper part of the siderite deposit is weathered and enriched to a mixture of iron and manganese oxides of direct shipping ore grade. Additional investigation of both the Karakuz and .Deveci mine areas is recommended including: 1. A detailed gravity and magnetic survey of part of the Karakuz area. 2. Diamond drilling at both the Karakuz and Deveci areas.

Open-File Report↗

USGS2009

Rock slope stability analysis along the North Carolina section of the Blue Ridge Parkway: Using a geographic information system (GIS) to integrate site data and digital geologic maps

In 2008, the North Carolina Geological Survey (NCGS) completed a five-year geologic and geohazards inventory of the 406-km long North Carolina segment of the Blue Ridge Parkway (BRP). The ArcGIS™ format deliverables for rock slopes include a slope movement and slope movement deposit database and maps and site-specific rock slope stability assessments at 158 locations. Database entries for known and potential rock slope failures include: location data, failure modes and dimensions, activity dates and levels, structural and lithologic data, the occurrence of sulfide minerals and acid-producing potential test results. Rock slope stability assessments include photographs of the rock cuts and show locations and orientations of rock data, seepage zones, and kinematic stability analyses. Assigned preliminary geologic hazard ratings of low, moderate and high indicate the generalized relative probability of rock fall and/or rock slide activity at a given location. Statistics compiled based on the database indicate some general patterns within the data. This information provides the National Park Service with tools that can aid in emergency preparedness, and in budgeting mitigation, maintenance and repair measures.

Conference Paper↗

USGS1966

Geochronology of the St. Kevin granite and neighboring precambrian rocks, northern Sawatch Range, Colorado

Radiometric ages have been measured on rocks of a crystalline terrane that includes ancient gneisses and migmatites, two granitic batholiths ( St . Kevin Granite and granite of Cross Creek), and various minor intrusive rocks . A whole- rock Rb-Sr isochron age on the St . Kevin Granite establishes it as 1390 ± 60 m.y. old. Mineral ages on the St . Kevin and numerous other rocks are either about the same as the St . Kevin whole- rock age or younger by as much as 200 m.y., even where the relative age is known to be older. Some minor Precambrian intrusive masses that are probably younger than St . Kevin Granite yield mica ages within analytical error of the St . Kevin age, indicating that these rocks can be younger than the granite by only a few tens of millions of years. The mica ages, both Rb-Sr and K-Ar, are thought to be minimal, but a K-Ar age of 2020 m.y. on horn-blende probably reflects excess argon. Mica ages from all rocks known geologically to be older than St . Kevin Granite are low and are interpreted as heating ages reflecting intrusion of the granite , in some cases modified further by heating during Laramide time. In this area, Precambrian intrusion and deformation had largely ended by 1200 or 1300 m.y. ago. Plutonism, represented here by the St . Kevin Granite and elsewhere by the Silver Plume and other granites, probably accounts for the numerous mineral ages of about 1300 m.y. previously reported from Colorado although weak regional metamorphism may also have been a factor.

Coloradao↗

USGS2008

U.S. Geological Survey Karst Interest Group Proceedings, Bowling Green, Kentucky, May 27-29, 2008

*INTRODUCTION AND ACKNOWLEDGMENTS* Karst aquifer systems are present throughout parts of the United States and some of its territories. The complex depositional environments that form carbonate rocks combined with post-depositional tectonic events and the diverse climatic regimes under which these rocks were formed result in unique hydrologic systems. The dissolution of calcium carbonate and the subsequent development of distinct and beautiful landscapes, caverns, and springs have resulted in some karst areas of the United States being designated as national or state parks and commercial caverns. Karst aquifers and landscapes that form in tropical areas, such as the north coast of Puerto Rico, differ greatly from karst areas in more arid climates, such as central Texas or western South Dakota. Many of these public and private lands contain unique flora and fauna associated with the hydrologic systems in these karst areas. As a result, multiple Federal, State, and local agencies have an interest in the study of karst terrains. Carbonate sediments and rocks (limestone and dolomite) are composed of greater than 50 percent carbonate minerals and the predominant carbonate mineral is calcium carbonate or limestone (CaCO3). Unlike terrigenous clastic sedimentation, the depositional processes that produce carbonate rocks are complex, involving both biological and physical processes. These depositional processes impact greatly the development of permeability of the sediments. Carbonate minerals readily dissolve or precipitate depending on the chemistry of the water flowing through the rock, thus the study of both marine and meteoric diagenesis of carbonate sediments is multidisciplinary. Even with a better understanding of the depositional environment and subsequent diagenesis, the dual porosity nature of karst aquifers presents challenges to scientists attempting to study ground-water flow and contaminant transport. Many of the major springs and aquifers in the United States are developed in carbonate rocks and karst areas. These aquifers and the springs that discharge from them, serve as major water-supply sources and as unique biological habitats. Commonly, there is competition for the water resources of karst aquifers, and urban development in karst areas can impact the ecosystem and water quality of these aquifers. The concept for developing a Karst Interest Group evolved from the November 1999 National Ground-Water Meeting of the U.S. Geological Survey (USGS), Water Resources Division. As a result, the Karst Interest Group was formed in 2000. The Karst Interest Group is a loose-knit grass-roots organization of USGS employees devoted to fostering better communication among scientists working on, or interested in, karst hydrology studies. The mission of the Karst Interest Group is to encourage and support interdisciplinary collaboration and technology transfer among USGS scientists working in karst areas. Additionally, the Karst Interest Group encourages cooperative studies between the different disciplines of the USGS and other Department of Interior agencies and university researchers or research institutes. The first Karst Interest Group workshop was held in St. Petersburg, Florida, February 13-16, 2001, in the vicinity of karst features of the Floridan aquifer system. The proceedings of that first meeting, Water-Resources Investigations Report 01-4011 are available online at: http://water.usgs.gov/ogw/karst/ The second Karst Interest Group workshop was held August 20-22, 2002, in Shepherdstown, West Virginia, in close proximity to the carbonate aquifers of the northern Shenandoah Valley. The proceedings of the second workshop were published in Water-Resources Investigations Report 02-4174, which is available online at the previously mentioned website. The third workshop of the Karst Interest Group was held September, 12-15, 2005, in Rapid City, South Dakota, which is in close proximity to karst features

Scientific Investigations Report↗

USGS2006

Gas-water-rock interactions in Frio Formation following CO 2 injection: Implications for the storage of greenhouse gases in sedimentary basins

To investigate the potential for the geologic storage of CO 2 in saline sedimentary aquifers, 1600 t of CO 2 were injected at 1500 m depth into a 24-m-thick sandstone section of the Frio Formation, a regional brine and oil reservoir in the U.S. Gulf Coast. Fluid samples obtained from the injection and observation wells before CO 2 injection showed a Na-Ca-Cl–type brine with 93,000 mg/L total dissolved solids (TDS) at near saturation with CH 4 at reservoir conditions. Following CO 2 breakthrough, samples showed sharp drops in pH (6.5–5.7), pronounced increases in alkalinity (100–3000 mg/L as HCO 3 ) and Fe (30–1100 mg/L), and significant shifts in the isotopic compositions of H 2 O, dissolved inorganic carbon (DIC), and CH 4 . Geochemical modeling indicates that brine pH would have dropped lower but for the buffering by dissolution of carbonate and iron oxyhydroxides. This rapid dissolution of carbonate and other minerals could ultimately create pathways in the rock seals or well cements for CO 2 and brine leakage. Dissolution of minerals, especially iron oxyhydroxides, could mobilize toxic trace metals and, where residual oil or suitable organics are present, the injected CO 2 could also mobilize toxic organic compounds. Environmental impacts could be major if large brine volumes with mobilized toxic metals and organics migrated into potable groundwater. The δ 18 O values for brine and CO 2 samples indicate that supercritical CO 2 comprises ∼50% of pore-fluid volume ∼6 mo after the end of injection. Postinjection sampling, coupled with geochemical modeling, indicates that the brine gradually will return to its preinjection composition.

Geology↗

USGS2011

40 Ar/ 39 Ar age-spectrum data for hornblende, biotite, white mica, and K-feldspar samples from metamorphic rocks in the Great Smoky Mountains of North Carolina and Tennessee

This report contains reduced 40 Ar/ 39 Ar data of hornblende, biotite, white mica and (or) sericite, and potassium-feldspar mineral separates and phyllite groundmass samples from metamorphic rocks of the Great Smoky Mountains in North Carolina and Tennessee. Included in this report are information on the location of the samples and a brief description of the samples. The data contained herein are not interpreted in a geological context, and care should be taken by users unfamiliar with argon isotopic data in the use of these results. No geological meaning is implied for any of the apparent ages presented below, and many of the individual apparent ages are not geologically meaningful. This report is primarily a detailed source document for subsequent publications that will integrate these data into a geological context. All the samples in this report were collected in and around the Great Smoky Mountain National Park in western North Carolina and eastern Tennessee.

North Carolina, Tennessee↗

USGS2012

Frictional properties of saponite-rich gouge from a serpentinite-bearing fault zone along the Gokasho-Arashima Tectonic Line, central Japan

We studied a serpentinite-bearing fault zone in Gokasho-Arashima Tectonic Line, Mie Prefecture, central Japan, characterizing its internal structures, mineral assemblage, permeability, and frictional properties. The fault core situated between the serpentinite breccia and the adjacent sedimentary rocks is characterized by a zone locally altered to saponite. The clayey gouge layer separates fault rocks of serpentinite origin containing talc and tremolite from fault rocks of sedimentary origin containing chlorite but no quartz. The minerals that formed within the fault are the products of metasomatic reaction between the serpentinite and the siliceous rocks. Permeability measurements show that serpentinite breccia and fault gouge have permeability of 10 −14 –10 −17 m 2 and 10 −15 –10 −18 m 2 , respectively, at 5–120 MPa confining pressure. Frictional coefficient of the saponite-rich clayey fault gouge ranged between 0.20 and 0.35 under room-dry condition, but was reduced to 0.06–0.12 when saturated with water. The velocity dependence of friction was strongly positive, mostly ranging between 0.005 and 0.006 in terms of a–b values. The governing friction law is not constrained yet, but we find that the saponite-rich gouge possesses an evolutional behavior in the opposite direction to that suggested by the rate and state friction law, in addition to its direct velocity dependence.

Journal of Structural Geology↗

USGS2009

Mississippi Valley-Type Lead-Zinc Deposit Model

Mississippi Valley-type (MVT) lead-zinc (Pb+Zn) deposits are found throughout the world, and these deposits are characteristically distributed over hundreds of square kilometers that define individual ore districts. The median size of individual MVT deposits is 7.0 million tonnes with grades of about 7.9 percent Pb+Zn metal. However, MVT deposits usually occur in extensive districts consisting of several to as many as 400 deposits. Nearly one-quarter of the world's sedimentary and volcanic rock-hosted Pb+Zn resources are found in these deposits, with by-product commodities including silver (Ag), copper (Cu), and indium (In) for some deposits. Environmentally, MVT deposits are less of a concern than other types of mineral deposits since the carbonate-host rocks mitigate many environmental concerns.

Open-File Report↗

USGS1978

Relation of Mercury, Uranium, and Lithium Deposits to the McDermitt Caldera Complex, Nevada-Oregon

The McDermitt caldera complex, located along the Nevada-Oregon border, is a Miocene collapse structure 45 kilometer in diameter. Large-volume rhyolitic and peralkaline ash-flow tuffs were erupted from 17.9 to 15.8 m.y. ago, leading to the formation of overlapping and nested calderas. Emplacement of rhyolitic ring domes, located primarily along the western margin of the calderas, represents the last phase of volcanic activity. The complex is the site of large deposits of mercury, an are deposit and several occurrences of uranium, and widespread occurrences of lithium. Mercury deposits at Cordero, McDermitt, Bretz, Ruja, and Opalite occur along ring fractures in sedimentary rocks that fill the calderas. Near the deposits the rocks are altered to zeolites and within the ore zones to potassium feldspar and silicate minerals. Although the mercury deposits contain anomalous concentrations of uranium, the most important uranium occurrences are restricted to rhyolitic ring domes emplaced along the western margin of the calderas. Lithium occurrences are located in tuffaceous rocks that are altered to zeolites and potassium feldspar. Concentrations of lithium ranging from 0.1 to 0.68 percent are associated with the clay mineral hectorite. The rhyolitic rocks erupted from the McDermitt caldera complex are enriched in mercury, uranium, and lithium and are likely source rocks for these elements in the ore deposits. Tuffaceous caldera fill-sediment averages 0.29 ppm mercury, 22 ppm uranium, and 236 ppm lithium; large-volume ash-flow tuffs contain up to 0.26 ppm mercury, 20 ppm uranium, and 300 ppm lithium.

Open-File Report↗

USGS2021

Geologic controls of slow-moving landslides near the U.S. West Coast

Slow-moving landslides, often with nearly imperceptible creeping motion, are an important landscape shaper and a dangerous natural hazard across the globe, yet their spatial distribution and geologic controls are still poorly known owing to a paucity of detailed, large-area observations. Here, we use interferometry of L-band satellite radar images to reveal 617 spatially large (4 × "> × 10 4 – 13 × "> × 10 6 m 2 ) and presently active (2007 – 2019) slow-moving landslides near the populous US West Coast (only 4.6% of these slides were previously known) and provide evidence for their fundamental controls by bedrock lithology and vertical land motion. We found that slow-moving landslides are generally larger and more spatially frequent in homogeneous bedrock with low rock strength, and they are preferentially located on hillslopes with geologically recent uplift. Notably, landslide size and spatial density in the relatively weak metamorphic rocks and mélange (due to pervasive tectonically sheared discontinuities, foliation, and abundant clay minerals) were two times larger than those in sedimentary and igneous rocks, and the hillslopes with landslides were found to be uplifting approximately three times faster than the average for the whole region. These results suggest that slow-moving landslides can be effectively uncovered by satellite radar imagery and their occurrence and character may be anticipated from vertical land uplift and bedrock lithology. Hence, our study provides understanding critical for reducing landslide hazards and quantifying landslide impacts on landscape change.

California, Oregon, Washington↗

USGS2004

Chapter 14 Rex Chert member of the Permian Phosphoria Formation: Composition, with emphasis on elements of environmental concern

We present bulk chemical and mineralogical compositions, as well as petrographic and outcrop descriptions, of rocks collected from three measured outcrop sections of the Rex Chert Member of the Phosphoria Formation in southeast Idaho. The three measured sections were chosen from 10 outcrops of Rex Chert that were described in the field. The Rex Chert overlies the Meade Peak Phosphatic Shale Member of the Phosphoria Formation, the source of phosphate ore in the region. Rex Chert removed as overburden constitutes part of the material transferred to waste-rock piles during phosphate mining. It is also used to surface roads in the mining district. It has been proposed that the chert be used to cap and isolate waste piles, thereby inhibiting the leaching of potentially toxic elements into the environment. The rock samples studied here are from individual chert beds representative of each stratigraphic section sampled. The Cherty Shale Member of the Phosphoria Formation that overlies the Rex Chert in measured section 1 and the upper Meade Peak and the transition zone to the Rex Chert in section 7 were also described and sampled. The cherts are predominantly spiculite composed of granular and mosaic quartz, and sponge spicules, with various but minor amounts of other fossils and detrital grains. The Cherty Shale Member and transition rocks between the Meade Peak and Rex Chert are siliceous siltstones and argillaceous cherts with ghosts of sponge spicules and somewhat more detrital grains than the chert. The dominant mineral is quartz. Carbonate beds are rare in each section and are composed predominantly of calcite and dolomite in addition to quartz. Feldspar, mica, clay minerals, calcite, dolomite, and carbonate fluorapatite are minor to trace minerals in the chert. The concentration of SiO 2 in the chert averages 94.6 wt.%. Organic-carbon content is generally very low, but can be as much as 1.8% in Cherty Shale Member samples and as much as 3.3% in samples from the transition between the Meade Peak and Rex Chert. Likewise, phosphate (P 2 O 5 ) is generally low in the chert, but can be as much as 3.1% in individual chert beds. Selenium concentrations in Rex Chert and Cherty Shale Member samples vary from <0.2 to 138 ppm, with a mean concentration of 7.0 ppm. This mean Se content is heavily dependent on two values of 101 and 138 ppm for siliceous siltstone from the lower part of the Rex Chert, which contains rocks that are transitional in character between the Meade Peak and Rex Chert Members. Without those two samples, the mean Se concentration is < 1.0 ppm. Other elements of environmental interest, As, Cr, V, Zn, Hg, and Cd, generally occur in concentrations near or below that in average continental shale. Stratigraphic changes, equivalent to temporal changes in the depositional basin, in chemical composition of rocks are notable either as uniform changes through the sections or as distinct differences in the mean composition of rocks that comprise the upper and lower halves of the sections. Q-mode factors are interpreted to represent the following rock and mineral components: chert-silica component consisting of Si (±Ba); phosphorite-carbonate fluorapatite component composed of P, Ca, As, Y, V, Cr, Sr, and La (± Fe, Zn, Cu, Ni, Li, Se, Nd, Hg); shale component composed of Al, Na, Zr, K, Ba, Li, and organic C (± Ti, Mg, Se, Ni, Fe, Sr, V, Mn, Zn); carbonate component (dolomite, calcite, silicified carbonates) composed of carbonate C, Mg, Ca, and Si (±Mn); and, tentatively, organic matter-hosted elements (and/or sulfide-sulfate phases) composed of Cu (± organic C, Zn, Mn, Si, Ni, Hg, Li). Selenium shows a dominant association with organic matter and to lesser degrees associations with other shale components and carbonate fluorapatite. Consideration of larger numbers of factors in Q-mode analysis indicates that native Se (a factor containing Se (± Ba)) may also comprise a minor component of the Se complement. Comparison of our data with those from newly exposed outcrops in active phosphate mines indicates that weathering of typical Rex Chert outcrops likely plays an important role in removing environmentally sensitive elements.

Idaho↗

USGS2016

High concentrations of manganese and sulfur in deposits on Murray Ridge, Endeavour Crater, Mars

Mars Reconnaissance Orbiter HiRISE images and Opportunity rover observations of the ~22 km wide Noachian age Endeavour Crater on Mars show that the rim and surrounding terrains were densely fractured during the impact crater-forming event. Fractures have also propagated upward into the overlying Burns formation sandstones. Opportunity’s observations show that the western crater rim segment, called Murray Ridge, is composed of impact breccias with basaltic compositions, as well as occasional fracture-filling calcium sulfate veins. Cook Haven, a gentle depression on Murray Ridge, and the site where Opportunity spent its sixth winter, exposes highly fractured, recessive outcrops that have relatively high concentrations of S and Cl, consistent with modest aqueous alteration. Opportunity’s rover wheels serendipitously excavated and overturned several small rocks from a Cook Haven fracture zone. Extensive measurement campaigns were conducted on two of them: Pinnacle Island and Stuart Island. These rocks have the highest concentrations of Mn and S measured to date by Opportunity and occur as a relatively bright sulfate-rich coating on basaltic rock, capped by a thin deposit of one or more dark Mn oxide phases intermixed with sulfate minerals. We infer from these unique Pinnacle Island and Stuart Island rock measurements that subsurface precipitation of sulfate-dominated coatings was followed by an interval of partial dissolution and reaction with one or more strong oxidants (e.g., O 2 ) to produce the Mn oxide mineral(s) intermixed with sulfate-rich salt coatings. In contrast to arid regions on Earth, where Mn oxides are widely incorporated into coatings on surface rocks, our results demonstrate that on Mars the most likely place to deposit and preserve Mn oxides was in fracture zones where migrating fluids intersected surface oxidants, forming precipitates shielded from subsequent physical erosion.

American Mineralogist↗

USGS1976

Identification of excess 40Ar by the 40Ar 39Ar, age spectrum technique

40 Ar/ 39 Ar incremental heating experiments on igneous plagioclase, biotite, and pyroxene that contain known amounts of excess 40 Ar indicate that saddle-shaped age spectra are diagnostic of excess 40 Ar in igneous minerals as well as in igneous rocks. The minima in the age spectra approach but do not reach the crystallization age. Neither the age spectrum diagram nor the 40 Ar/ 36 Ar versus 39 Ar/ 36 Ar isochron diagram reliably reveal the crystallization age in such samples.

Earth and Planetary Science Letters↗

USGS2011

Diffusion-driven magnesium and iron isotope fractionation in Hawaiian olivine

Diffusion plays an important role in Earth sciences to estimate the timescales of geological processes such as erosion, sediment burial, and magma cooling. In igneous systems, these diffusive processes are recorded in the form of crystal zoning. However, meaningful interpretation of these signatures is often hampered by the fact that they cannot be unambiguously ascribed to a single process (e.g., magmatic fractionation, diffusion limited transport in the crystal or in the liquid). Here we show that Mg and Fe isotope fractionations in olivine crystals can be used to trace diffusive processes in magmatic systems. Over sixty olivine fragments from Hawaiian basalts show isotopically fractionated Mg and Fe relative to basalts worldwide, with up to 0.4‰ variation in 26 Mg/ 24 Mg ratios and 1.6‰ variation in 56 Fe/ 54 Fe ratios. The linearly and negatively correlated Mg and Fe isotopic compositions [i.e., δ 56 Fe = (− 3.3 ± 0.3) × δ 26 Mg], co-variations of Mg and Fe isotopic compositions with Fe/Mg ratios of olivine fragments, and modeling results based on Mg and Fe elemental profiles demonstrate the coupled Mg and Fe isotope fractionation to be a manifestation of Mg–Fe inter-diffusion in zoned olivines during magmatic differentiation. This characteristic can be used to constrain the nature of mineral zoning in igneous and metamorphic rocks, and hence determine the residence times of crystals in magmas, the composition of primary melts, and the duration of metamorphic events. With improvements in methodology, in situ isotope mapping will become an essential tool of petrology to identify diffusion in crystals.

Hawaii↗

USGS2006

Iron isotope fractionation during microbially stimulated Fe(II) oxidation and Fe(III) precipitation

Interpretation of the origins of iron-bearing minerals preserved in modern and ancient rocks based on measured iron isotope ratios depends on our ability to distinguish between biological and non-biological iron isotope fractionation processes. In this study, we compared 56Fe/54Fe ratios of coexisting aqueous iron (Fe(II)aq, Fe(III)aq) and iron oxyhydroxide precipitates (Fe(III)ppt) resulting from the oxidation of ferrous iron under experimental conditions at low pH (<3). Experiments were carried out using both pure cultures of Acidothiobacillus ferrooxidans and sterile controls to assess possible biological overprinting of non-biological fractionation, and both SO42- and Cl- salts as Fe(II) sources to determine possible ionic/speciation effects that may be associated with oxidation/precipitation reactions. In addition, a series of ferric iron precipitation experiments were performed at pH ranging from 1.9 to 3.5 to determine if different precipitation rates cause differences in the isotopic composition of the iron oxyhydroxides. During microbially stimulated Fe(II) oxidation in both the sulfate and chloride systems, 56Fe/54Fe ratios of residual Fe(II)aq sampled in a time series evolved along an apparent Rayleigh trend characterized by a fractionation factor ??Fe(III)aq-Fe(II)aq???1.0022. This fractionation factor was significantly less than that measured in our sterile control experiments (???1.0034) and that predicted for isotopic equilibrium between Fe(II)aq and Fe(III)aq (???1.0029), and thus might be interpreted to reflect a biological isotope effect. However, in our biological experiments the measured difference in 56Fe/54Fe ratios between Fe(III)aq, isolated as a solid by the addition of NaOH to the final solution at each time point under N2-atmosphere, and Fe(II)aq was in most cases and on average close to 2.9??? (??Fe(III)aq-Fe(II)aq ???1.0029), consistent with isotopic equilibrium between Fe(II)aq and Fe(III)aq. The ferric iron precipitation experiments revealed that 56Fe/54Fe ratios of Fe(III)aq were generally equal to or greater than those of Fe(III)ppt, and isotopic fractionation between these phases decreased with increasing precipitation rate and decreasing grain size. Considered together, the data confirm that the iron isotope variations observed in our microbial experiments are primarily controlled by non-biological equilibrium and kinetic factors, a result that aids our ability to interpret present-day iron cycling processes but further complicates our ability to use iron isotopes alone to identify biological processing in the rock record. ?? 2005 Elsevier Inc. All rights reserved.

Geochimica et Cosmochimica Acta↗

USGS2007

Controls on the Karaha-Telaga Bodas geothermal reservoir, Indonesia

Karaha-Telaga Bodas is a partially vapor-dominated, fracture-controlled geothermal system located adjacent to Galunggung Volcano in western Java, Indonesia. The geothermal system consists of: (1) a caprock, ranging from several hundred to 1600 m in thickness, and characterized by a steep, conductive temperature gradient and low permeability; (2) an underlying vapor-dominated zone that extends below sea level; and (3) a deep liquid-dominated zone with measured temperatures up to 353 ??C. Heat is provided by a tabular granodiorite stock encountered at about 3 km depth. A structural analysis of the geothermal system shows that the effective base of the reservoir is controlled either by the boundary between brittle and ductile deformational regimes or by the closure and collapse of fractures within volcanic rocks located above the brittle/ductile transition. The base of the caprock is determined by the distribution of initially low-permeability lithologies above the reservoir; the extent of pervasive clay alteration that has significantly reduced primary rock permeabilities; the distribution of secondary minerals deposited by descending waters; and, locally, by a downward change from a strike-slip to an extensional stress regime. Fluid-producing zones are controlled by both matrix and fracture permeabilities. High matrix permeabilities are associated with lacustrine, pyroclastic, and epiclastic deposits. Productive fractures are those showing the greatest tendency to slip and dilate under the present-day stress conditions. Although the reservoir appears to be in pressure communication across its length, fluid, and gas chemistries vary laterally, suggesting the presence of isolated convection cells. ?? 2006 CNR.

Geothermics↗

USGS2014

Hematite-bearing materials surrounding Candor Mensa in Candor Chasma, Mars: Implications for hematite origin and post-emplacement modification

The Valles Marineris canyon system on Mars is of enduring scientific interest in part due to the presence of interior mounds that contain extensive layering and water-altered minerals, such as crystalline gray hematite and hydrated sulfates. The presence of hematite and hydrated sulfate minerals is important because their host rock lithologies provide information about past environments that may have supported liquid water and may have been habitable. This work further defines the association and relationship between hematite-bearing materials and low albedo (presumably aeolian) deposits and layered materials, identifies physical characteristics that are strongly correlated with the presence of hematite, and refines hypotheses for the origin and post-emplacement modification (including transport) of these hematite-bearing and associated materials. There are only three regions surrounding Candor Mensa where hematite has been identified, even though morphologic properties are similar throughout the entire mensa. Three possible explanations for why hematite is only exposed in these regions include: (1) the topographic structure of the mensa walls concentrates hematite at the base of the layered deposits, influencing the ability to detect hematite from orbit; (2) the presence of differing amounts of “dark mantling material” and hematite-free erosional sediment; (3) the potential fracturing of the mensa and the influence of these structures on fluid flow and subsequent digenesis. The observations of hematite-bearing materials in this work support the hypothesis that hematite is eroding from a unit in the Candor Mensa interior layered deposits (ILD) and is being concentrated as a lag deposit adjacent to the lower layers of Candor Mensa and at the base in the form of dark aeolian material. Due to the similar geologic context associated with hematite-bearing and ILD materials throughout the Valles Marineris canyon system, the insight gained from studying these materials surrounding Candor Mensa can likely be applicable to similar layered deposits throughout Valles Marineris.

Icarus↗

USGS1997

Environmental geochemistry of shale-hosted Ag-Pb-Zn massive sulfide deposits in northwest Alaska: Natural background concentrations of metals in water from mineralized areas

Red Dog, Lik and Drenchwater are shale-hosted stratiform Ag-Pb-Zn massive sulfide deposits in the northwestern Brooks Range. Natural background concentrations of metals in waters from the undisturbed (unmined) Drenchwater prospect and Lik deposit were compared to pre-mining baseline studies conducted at Red Dog. The primary factors affecting water chemistry are the extent of exposure of the deposits, the grade of mineralization, the presence of carbonate reeks in the section, and the proportion of Fe-sulfide in the ore. Surface water samples from the Drenchwater prospect, which has pyrite-dominant mineralization exposed in outcrop, have pH values as low as 2.8 and high dissolved concentrations of metals including as much as 95 mg 1-1 Al, 270 mg 1-1 Fe, 8 ??1-1 Cd, 10 ??1-1 Pb, and 2600 ??1-1 Zn, with As up to 26 ??g1-1. Surface waters from the Red Dog deposit prior to mining were also acidic and metal-rich, however, dissolved metal concentrations in Red Dog waters were many times greater. The higher metal concentrations in Red Dog waters reflect the high Zn grades and the abundant sphalerite, pyrite, and galena that were present in outcrop prior to mining. In contrast, despite significant mineralization at the Lik deposit, carbonate rocks in the section buffer the system, resulting in less acidic, mostly near-neutral pH values with low concentrations of most metals except Zn.

Applied Geochemistry↗