underlying carbonate rocks: Topics by Science.gov

Sample records for underlying carbonate rocks

Laboratory measurements of the effective-stress law of carbonate rocks under deformation

DOE Office of Scientific and Technical Information (OSTI.GOV)

Warpinski, N.R.; Teufel, L.W.

The behavior of rocks under the combined effects of confining stress and pore pressure is an important issue for any in situ petroleum process. In order to simplify the difficulties in dealing with two independent parameters, it is customary to introduce an effective-stress law which relates a net, or effective, stress to some combination of confining stress and pore pressure. This report documents laboratory tests of mechanical properties of five carbonate rocks.
Evolution of strength and physical properties of carbonate and ultramafic rocks under hydrothermal conditions

NASA Astrophysics Data System (ADS)

Lisabeth, Harrison Paul

Interaction of rocks with fluids can significantly change mineral assemblage and structure. This so-called hydrothermal alteration is ubiquitous in the Earth's crust. Though the behavior of hydrothermally altered rocks can have planet-scale consequences, such as facilitating oceanic spreading along slow ridge segments and recycling volatiles into the mantle at subduction zones, the mechanisms involved in the hydrothermal alteration are often microscopic. Fluid-rock interactions take place where the fluid and rock meet. Fluid distribution, flux rate and reactive surface area control the efficiency and extent of hydrothermal alteration. Fluid-rock interactions, such as dissolution, precipitation and fluid mediated fracture and frictional sliding lead to changes in porosity and pore structure that feed back into the hydraulic and mechanical behavior of the bulk rock. Examining the nature of this highly coupled system involves coordinating observations of the mineralogy and structure of naturally altered rocks and laboratory investigation of the fine scale mechanisms of transformation under controlled conditions. In this study, I focus on fluid-rock interactions involving two common lithologies, carbonates and ultramafics, in order to elucidate the coupling between mechanical, hydraulic and chemical processes in these rocks. I perform constant strain-rate triaxial deformation and constant-stress creep tests on several suites of samples while monitoring the evolution of sample strain, permeability and physical properties. Subsequent microstructures are analyzed using optical and scanning electron microscopy. This work yields laboratory-based constraints on the extent and mechanisms of water weakening in carbonates and carbonation reactions in ultramafic rocks. I find that inundation with pore fluid thereby reducing permeability. This effect is sensitive to pore fluid saturation with respect to calcium carbonate. Fluid inundation weakens dunites as well. The addition of carbon dioxide to pore fluid enhances compaction and partial recovery of strength compared to pure water samples. Enhanced compaction in CO2-rich fluid samples is not accompanied by enhanced permeability reduction. Analysis of sample microstructures indicates that precipitation of carbonates along fracture surfaces is responsible for the partial restrengthening and channelized dissolution of olivine is responsible for permeability maintenance.
Hydrogeology and potential for ground-water development, carbonate-rock aquifers in southern Nevada and southeastern California

USGS Publications Warehouse

Burbey, T.J.

1997-01-01

Seventeen hydrographic areas in southern Nevada were assessed for the ground-water development potential of the underlying carbonate-rock aquifers on the basis of geologic and hydrologic information developed as part of the Nevada Carbonate Aquifers Study and information compiled from previous investigations. All selected areas lie within a miogeoclinal belt where thick accumulations of carbonate rock followed by major episodes of compression and extension have greatly modified the region. Most of the selected hydrographic areas lie within the less extended terranes; however, several areas, or parts of areas, lie within severely extended terranes where carbonate rocks have been greatly thinned, or where deformed blocks of carbonate rock are discontinuous and isolated from surrounding carbonate rock aquifers. Three principal criteria were used to assess the development potential of each selected hydrographic area. These quantitative criteria are: (1) depth to water, (2) depth to and thickness of carbonate rocks, and (3) water quality. Other site-specific factors, such as accessibility and potential effects of ground-water development, are also discussed. Results suggest that sites with high potential for development may be scarce in southern Nevada. Many areas described as favorable on the basis of the three quantitative criteria were deemed unfavorable on the basis of possible short- and long-term effects associated with development and on the amount of available data used to make the assessment. The most favorable sites may be in more severely extended terranes, where development of isolated blocks (of carbonate-rock aquifer material) would be less likely to affect neighboring areas.
Carbonate hosted fault rocks: A review of structural and microstructural characteristic with implications for seismicity in the upper crust

NASA Astrophysics Data System (ADS)

Delle Piane, Claudio; Clennell, M. Ben; Keller, Joao V. A.; Giwelli, Ausama; Luzin, Vladimir

2017-10-01

The structure, frictional properties and permeability of faults within carbonate rocks exhibit a dynamic interplay that controls both seismicity and the exchange of fluid between different crustal levels. Here we review field and experimental studies focused on the characterization of fault zones in carbonate rocks with the aim of identifying the microstructural indicators of rupture nucleation and seismic slip. We highlight results from experimental research linked to observations on exhumed fault zones in carbonate rocks. From the analysis of these accumulated results we identify the meso and microstructural deformation styles in carbonates rocks and link them to the lithology of the protolith and their potential as seismic indicators. Although there has been significant success in the laboratory reproduction of deformation structures observed in the field, the range of slip rates and dynamic friction under which most of the potential seismic indicators is formed in the laboratory urges caution when using them as a diagnostic for seismic slip. We finally outline what we think are key topics for future research that would lead to a more in-depth understanding of the record of seismic slip in carbonate rocks.
The effect of carbon-rich fluid alteration on the mechanical and physical properties of ultramafic rocks from Linnejavrre, Norway

NASA Astrophysics Data System (ADS)

Lisabeth, H. P.; Zhu, W.

2016-12-01

Carbon dioxide interacts with mafic and ultramafic rocks on the ocean floor at fracture zones and detachment faults, and within ophiolite complexes. Steatized olivine-pyroxene or serpentinite rocks become talc-carbonate rocks, i.e., soapstones. If the fluids are extremely carbon-rich, the process can continue to completion, binding all the magnesium from olivine and pyroxene in magnesium carbonate, resulting in magnesite-quartz rocks known as listvenites. The structural, mechanical and mineralogical characteristics of these rocks can be long-lived and affect later tectonic deformation over the course of the supercontinent cycle, influencing the obduction of ophiolites and possibly the initiation of subduction. To ascertain the changes in physical and geomechanical characteristics of these rocks as they undergo carbonic alteration, we measure ultrasonic velocity, electrical resistivity and shear strength in a series of laboratory tests on samples collected from northern Norway, where the Linnajavrre Ophiolite contains representative samples of serpentinite, soapstone and listvenite. We discover that the rocks tend to become denser, more porous, weaker, and more electrically and acoustically impeditive as carbonation proceeds. Samples fail by highly localized brittle faulting with little dilatancy. Shear strength appears to correlate with talc abundance, with a steep drop-off from 5 to 20% talc. Deformed samples are examined under petrographic microscope to explore deformation micromechanisms. Our data suggest that the weakening observed in soapstones and listvenites compared to serpentinites is attributed to interconnected talc grains. Such carbonic alteration of oceanic serpentinites may help facilitate oceanic spreading, particularly along slow and ultraslow segments of mid-ocean ridges.
The role of forest trees and their mycorrhizal fungi in carbonate rock weathering and its significance for global carbon cycling.

PubMed

Thorley, Rachel M S; Taylor, Lyla L; Banwart, Steve A; Leake, Jonathan R; Beerling, David J

2015-09-01

On million-year timescales, carbonate rock weathering exerts no net effect on atmospheric CO2 concentration. However, on timescales of decades-to-centuries, it can contribute to sequestration of anthropogenic CO2 and increase land-ocean alkalinity flux, counteracting ocean acidification. Historical evidence indicates this flux is sensitive to land use change, and recent experimental evidence suggests that trees and their associated soil microbial communities are major drivers of continental mineral weathering. Here, we review key physical and chemical mechanisms by which the symbiotic mycorrhizal fungi of forest tree roots potentially enhance carbonate rock weathering. Evidence from our ongoing field study at the UK's national pinetum confirms increased weathering of carbonate rocks by a wide range of gymnosperm and angiosperm tree species that form arbuscular (AM) or ectomycorrhizal (EM) fungal partnerships. We demonstrate that calcite-containing rock grains under EM tree species weather significantly faster than those under AM trees, an effect linked to greater soil acidification by EM trees. Weathering and corresponding alkalinity export are likely to increase with rising atmospheric CO2 and associated climate change. Our analyses suggest that strategic planting of fast-growing EM angiosperm taxa on calcite- and dolomite-rich terrain might accelerate the transient sink for atmospheric CO2 and slow rates of ocean acidification. © 2014 The Authors. Plant, Cell & Environment published by John Wiley & Sons Ltd.
Effects of karst and geologic structure on the circulation of water and permeability in carbonate aquifers

USGS Publications Warehouse

Stringfield, V.T.; Rapp, J.R.; Anders, R.B.

1979-01-01

The results of the natural processes caused by solution and leaching of limestone, dolomite, gypsum, salt and other soluble rocks, is known as karst. Development of karst is commonly known as karstification, which may have a pronounced effect on the topography, hydrology and environment, especially where such karst features as sinkholes and vertical solution shafts extend below the land surface and intersect lateral solution passages, cavities, caverns and other karst features in carbonate rocks. Karst features may be divided into two groups: (1) surficial features that do not extend far below the surface; and (2) karst features such as sinkholes that extend below the surface and affect the circulation of water below. The permeability of the most productive carbonate aquifers is due chiefly to enlargement of fractures and other openings by circulation of water. Important controlling factors responsible for the development of karst and permeability in carbonate aquifers include: (1) climate, topography, and presence of soluble rocks; (2) geologic structure; (3) nature of underground circulation; and (4) base level. Another important factor is the condition of the surface of the carbonate rocks at the time they are exposed to meteoric water. A carbonate rock surface, with soil or relatively permeable, less soluble cover, is more favorable for initiation of karstification and solution than bare rocks. Water percolates downward through the cover to the underlying carbonate rocks instead of running off on the surface. Also, the water becomes more corrosive as it percolates through the permeable cover to the underlying carbonate rocks. Where there is no cover or the cover has been removed, the carbonate rocks become case hardened and resistant to erosion. However, in regions underlain not only by carbonate rocks but also by beds of anhydrite, gypsum and salt, such as the Hueco Plateau in southeastern New Mexico, subsurface solution may occur where water without natural acids moves down from bare rock surfaces through cracks to the beds that are more soluble than carbonate rocks. For example, in the area of Carlsbad Caverns in southeastern New Mexico, much of the water responsible for solution that formed the caverns apparently entered the groundwater system through large open fractures and did not form sinkhole topography. East of the Carlsbad Caverns, however, in the Pecos River Valley where the carbonate rocks are overlain by the less soluble Ogallala Formation of Late Tertiary age, solution began along escarpments as the Pecos River and its tributaries cut through the less soluble cover. As these escarpments retreated, sinkholes and other karst features developed. Joints or fractures are essential for initiation of downward percolation of water in compact carbonate rocks such as some Paleozoic limestone in which there is no intergranular permeability. Also joints or fractures and bedding planes may be essential in the initiation of lateral movement of water in the zone of saturation. Where conditions of recharge and discharge are favorable, groundwater may move parallel to the dip. However, the direction of movement of water in most carbonate rocks is not necessarily down dip or parallel to the dip. The general direction of movement of both surface and groundwater may be parallel to the strike in a breached anticline. Faults may restrict the lateral movement of water, especially if water-bearing beds are faulted against relatively impervious beds. Conversely, some fault may serve as avenues through which water may move as, for example, in the Cretaceous Edwards aquifer in the San Antonio area, Texas. Karst aquifers, chiefly carbonate rocks, may be placed in three groups according to water-bearing capacity. Water in aquifers of group 1 occurs chiefly in joints, fractures, and other openings that have not been enlarged by solution. The yield of wells is small. Aquifers in group 2, with low to intermediate yields, are those in which
Susceptibility of Granite Rock to scCO2/Water at 200 degrees C and 250 degrees C

DOE Office of Scientific and Technical Information (OSTI.GOV)

Sugama, T.; Gill, S., Ecker, L., Butcher, T., Warren, J.

Granite rock comprising anorthoclase-type albite and quartz as its major phases and biotite mica as the minor one was exposed to supercritical carbon dioxide (scCO{sub 2})/water at 250 C and 13.78 MPa pressure for 104 hours. For comparison purpose, four other rocks, albite, hornblende, diorite, and quartz, also were exposed. During the exposure of granite, ionic carbonic acid, known as the wet carbonation reactant, preferentially reacted with anorthoclase-type albite and biotite, rather than with quartz. The susceptibility of biotite to wet carbonation was higher than that of anorthoclase-type albite. All the carbonation by-products of anorthoclase-type albite were amorphous phases includingmore » Na- and K-carbonates, a kaolinite clay-like compound, and silicon dioxide, while wet carbonation converted biotite into potassium aluminum silicate, siderite, and magnesite in crystalline phases and hydrogen fluoride (HF). Three of these reaction by-products, Na- and K-carbonates and HF, were highly soluble in water. Correspondingly, the carbonated top surface layer, about 1.27 mm thick as carbonation depth, developed porous microstructure with numerous large voids, some of which have a size of {>=} 10 {mu}m, reflecting the erosion of granite by the leaching of these water-soluble reaction by-products. Comparing with this carbonation depth, its depth of other minerals was considerable lower, particularly, for hornblende and diorite with 0.07 and 0.02 mm, while no carbonate compound was detected in quartz. The major factor governing these low carbonation depths in these rocks was the formation of water-insensitive scale-like carbonate by-products such as calcite (CaCO{sub 3}), siderite (FeCO{sub 3}), and magnesite (MgCO{sub 3}). Their formation within the superficial layer of these minerals served as protective barrier layer that inhibits and retards further carbonation of fresh underlying minerals, even if the exposure time was extended. Thus, the coverage by this barrier layer of the non-carbonated surfaces of the underlying rock was reason why the hornblende and diorite exhibited a minimum depth of carbonation. Under exposure to the scCO{sub 2}/water at 200 C and 10.34 MPa pressure for up to 42 days, the ranking of the magnitude of erosion caused by wet carbonation was in the following order; granite > albite > hornblende > diorite > quartz. The eroding-caused weight loss of granite (0.88 %) was {approx}2.4, {approx}5.2, {approx}9.8, and {approx}17.6 times greater than that of albite, hornblends, diorite, and quartz, respectively.« less
The Time-Dependency of Deformation in Porous Carbonate Rocks

NASA Astrophysics Data System (ADS)

Kibikas, W. M.; Lisabeth, H. P.; Zhu, W.

2016-12-01

Porous carbonate rocks are natural reservoirs for freshwater and hydrocarbons. More recently, due to their potential for geothermal energy generation as well as carbon sequestration, there are renewed interests in better understanding of the deformation behavior of carbonate rocks. We conducted a series of deformation experiments to investigate the effects of strain rate and pore fluid chemistry on rock strength and transport properties of porous limestones. Indiana limestone samples with initial porosity of 16% are deformed at 25 °C under effective pressures of 10, 30, and 50 MPa. Under nominally dry conditions, the limestone samples are deformed under 3 different strain rates, 1.5 x 10-4 s-1, 1.5 x 10-5 s-1 and 1.5 x 10-6 s-1 respectively. The experimental results indicate that the mechanical behavior is both rate- and pressure-dependent. At low confining pressures, post-yielding deformation changes from predominantly strain softening to strain hardening as strain rate decreases. At high confining pressures, while all samples exhibit shear-enhanced compaction, decreasing strain rate leads to an increase in compaction. Slower strain rates enhance compaction at all confining pressure conditions. The rate-dependence of deformation behaviors of porous carbonate rocks at dry conditions indicates there is a strong visco-elastic coupling for the degradation of elastic modulus with increasing plastic deformation. In fluid saturated samples, inelastic strain of limestone is partitioned among low temperature plasticity, cataclasis and solution transport. Comparison of inelastic behaviors of samples deformed with distilled water and CO2-saturated aqueous solution as pore fluids provide experimental constraints on the relative activities of the various mechanisms. Detailed microstructural analysis is conducted to take into account the links between stress, microstructure and the inelastic behavior and failure mechanisms.
Age of Walden Creek Group: Can it be demonstrated--Biostratigraphically

DOE Office of Scientific and Technical Information (OSTI.GOV)

Broadhead, T.W.; Hatcher, R.D. Jr.; Walker, K.R.

The Walden Creek Group (WCG) is a lithologically heterogeneous succession of sedimentary rocks exposed in the western Blue Ridge of the southern Appalachians. Carbonate rocks of the WCG occur as bedded limestone in the Sandsuck Formation and subjacent Wilhite and as limestone clasts in polymict conglomerate bodies within the Sandsuck, Wilhite, and the underlying Shields Formation. Petrographically, these carbonate rocks exhibit a shallow marine aspect. Locally abundant pisoids, ooids and peloids occur in a preservational continuum ranging from well-preserved internal fabrics to relict spar-filled micrite envelopes. Pisoids, occurring in grainstone and wackestone fabrics, resemble oversized marine ooids characteristic of Uppermore » Proterozoic carbonated rocks of Greenland and Spitzbergen. Recent reports of metazoan and foraminiferal fossils from the Wilhite Formation have cast doubt on its long-regarded Late Proterozoic age. The fossils the authors have observed include algal oncolites, minute fecal pellets, and extremely rare cyanobacterial filament sheaths and skeletal fragments of uncertain biological affinity. Good quality preservation of allochems in WCG carbonate rocks is important in evaluating the absence of undoubted Paleozoic fossils. Dominant components of Paleozoic biotas: crinoids, brachiopods, and bryozoans would be recognizable, even as tiny fragments. The absence of conodonts further suggests that carbonate rocks of the WCG predate the appearance of abundant skeletonized biota and are probably Late Proterozoic. The authors propose that both bedded carbonate rocks and carbonate clasts of the WCG are essentially contemporaneous with each other and reflect carbonate bank conditions that developed toward the end of Late Proterozoic clastic deposition, which filled rift basins that formed along the southeastern Laurentian margin. Episodic reactivation accounts for the occurrence of carbonate clasts in several parts of the WCG and Snowbird Group.« less
[Difference of Karst Carbon Sink Under Different Land Use and Land Cover Areas in Dry Season].

PubMed

Zhao, Rui-yi; Liang, Zuo-bing; Wang, Zun-bo; Yu, Zheng-liang; Jiang, Ze-li

2015-05-01

In order to identify the distinction of soil CO2 consumed by carbonate rock dissolution, Baishuwan spring, Lanhuagou spring and Hougou spring were selected as objects to monitor the hydrochemistry from November 2013 to May 2014. The results showed that the highest HCO3- concentration was observed in Baishuwan spring which is covered by pine forest, while the lowest HCO3- concentration was observed in Hougou spring which is mainly covered by cultivated land. In Baishuwan spring, HCO3- was mainly derived from carbonic acid dissolving carbonate rock and the molar ratio between Ca(2+) + Mg2+ and HCO3- was close to 0. 5; while the molar ratio between Ca(2+) + Mg2+ and HCO3- exceeded 0.5 because the carbonate rock in Lanhuagou spring and Hougou spring was mainly dissolved by nitric acid and sulfuric acid. Because of the input of litter and the fact that gas-permeability of soil was limited in Baishuwan spring catchment, most of soil CO2 was dissolved in infiltrated water and reacted with bedrock. However, in Lanhuagou spring catchment and Hougou spring catchment, porous soil made soil CO2 easier to return to the atmosphere in the form of soil respiration. Therefore, in order to accurately estimate karst carbon sink, it was required to clarify the distinction of CO2 consumption by carbonate rock dissolution under different land use and land cover areas.
Sulfate-dependent Anaerobic Oxidation of Methane as a Generation Mechanism for Calcite Cap Rock in Gulf Coast Salt Domes

NASA Astrophysics Data System (ADS)

Caesar, K. H.; Kyle, R.; Lyons, T. W.; Loyd, S. J.

2015-12-01

Gulf Coast salt domes, specifically their calcite cap rocks, have been widely recognized for their association with significant reserves of crude oil and natural gas. However, the specific microbial reactions that facilitate the precipitation of these cap rocks are still largely unknown. Insight into the mineralization mechanism(s) can be obtained from the specific geochemical signatures recorded in these structures. Gulf Coast cap rocks contain carbonate and sulfur minerals that exhibit variable carbon (d13C) and sulfur isotope (δ34S) signatures. Calcite d13C values are isotopically depleted and show a large range of values from -1 to -52‰, reflecting a mixture of various carbon sources including a substantial methane component. These depleted carbon isotope compositions combined with the presence of abundant sulfide minerals in cap rocks have led to interpretations that invoke microbial sulfate reduction as an important carbonate mineral-yielding process in salt dome environments. Sulfur isotope data from carbonate-associated sulfate (CAS: trace sulfate incorporated within the carbonate mineral crystal lattice) provide a more direct proxy for aqueous sulfate in salt dome systems and may provide a means to directly fingerprint ancient sulfate reduction. We find CAS sulfur isotope compositions (δ34SCAS) significantly greater than those of the precursor Jurassic sulfate-salt deposits (which exhibit δ34S values of ~ +15‰). This implies that cap rock carbonate generation occurred via microbial sulfate reduction under closed-system conditions. The co-occurrence of depleted carbonate d13C values (< ~30‰) and the enriched δ34SCAS values are evidence for sulfate-dependent anaerobic oxidation of methane (AOM). AOM, which has been shown to yield extensive seafloor carbonate authigenesis, is also potentially partly responsible for the carbonate minerals of the Gulf Coast calcite cap rocks through concomitant production of alkalinity. Collectively, these data shed new light on a potential hotspot of microbial activity in the deep biosphere.
Methane and carbon at equilibrium in source rocks

PubMed Central

2013-01-01

Methane in source rocks may not exist exclusively as free gas. It could exist in equilibrium with carbon and higher hydrocarbons: CH4 + C < = > Hydrocarbon. Three lines of evidence support this possibility. 1) Shales ingest gas in amounts and selectivities consistent with gas-carbon equilibrium. There is a 50% increase in solid hydrocarbon mass when Fayetteville Shale is exposed to methane (450 psi) under moderate conditions (100°C): Rock-Eval S2 (mg g-1) 8.5 = > 12.5. All light hydrocarbons are ingested, but with high selectivity, consistent with competitive addition to receptor sites in a growing polymer. Mowry Shale ingests butane vigorously from argon, for example, but not from methane under the same conditions. 2) Production data for a well producing from Fayetteville Shale declines along the theoretical curve for withdrawing gas from higher hydrocarbons in equilibrium with carbon. 3) A new general gas-solid equilibrium model accounts for natural gas at thermodynamic equilibrium, and C6-C7 hydrocarbons constrained to invariant compositions. The results make a strong case for methane in equilibrium with carbon and higher hydrocarbons. If correct, the higher hydrocarbons in source rocks are gas reservoirs, raising the possibility of substantially more gas in shales than analytically apparent, and far more gas in shale deposits than currently recognized. PMID:24330266
Mineralization of atmospheric CO2 via fluid reaction with mafic/ultramafic rocks

NASA Astrophysics Data System (ADS)

Westfield, I. T.; Kendall, T. A.; Ries, J. B.

2011-12-01

Atmospheric CO2 has increased nearly 50% since the Industrial Revolution, due primarily to increased fossil fuel combustion, cement production, and deforestation. Although subterranean reservoirs are presently considered the most viable sink for anthropogenically liberated CO2, concerns exist over the stability of these systems and their impacts on regional tectonics, aquifers, and subterranean microbial ecosystems. Direct mineralization of CO2 at the Earth's surface provides an alternative capable of generating useful carbon-negative mineral byproducts that may be used to supplement or replace conventional carbon-positive building materials, like cement. However, mineralization of anthropogenic CO2 requires large sources of alkalinity to convert CO2 to CO32-, and divalent cations (e.g., Mg2+, Ca2+, Fe2+, etc.) to bond with the aqueous CO32-. Ultramafic and mafic rocks, such as peridotites, serpentinites, and basalts, are globally abundant, naturally occurring sources of the divalent cations, and alkalinity required for CO2 mineralization. Here, we present the results of accelerated reactions between ultramafic/mafic rocks, water, and CO2/N2 gases, aimed at quantifying the carbonation potential of mafic/ultramafic rocks. Rock-fluid-gas batch reactions were carried out in vented 4 L borosilicate glass flasks filled with 3 L DI water and 200 g acetone-washed, 49-180μm-diameter grains of four ultramafic/mafic rock types: peridotite, dunite, websterite and basalt. Each of the four rock-water mixtures was reacted under pure CO2 and pure N2 and at 25 and 200 °C, for a total of 16 reactions. Mixtures were continuously heated and stirred for 14 days. Samples (330 mL) were obtained at 0, 1, 6, 24, 48, 96, 168, and 336 hrs and filtered at 0.4 μm. The pH of filtered samples was measured with a single-junction Ag/AgCl glass electrode, salinity was determined with a conductivity probe, total alkalinity (TA) was determined by closed-cell potentiometric Gran titration, and DIC was determined by coulometry (all calibrated with certified reference materials). [CO32-], [HCO3-], and [OH-] were calculated from TA and DIC. For all reactions, pH (range: 5.5 - 9.7), TA, DIC, [CO32-], and [HCO3-] increased dramatically within the first several hours of the experiment, and then either steadily increased, plateaued, or declined, in some cases increasing again after the decline. After the initial spike, DIC increased with time under 25 °C, but decreased under 200 °C. Salinity and [OH-] increased steadily throughout most reactions. Lack of correlation of abrupt, short-lived declines in pH, TA, DIC, [CO32-], and [HCO3-] with [OH-] between 24 and 48 hrs at 200 °C suggests sudden precipitation of carbonate minerals, rather than production of silicic acid. Temperature generally increased reaction rates to a greater extent under CO2 than under N2, and substantially more OH- ions were liberated from rocks at 200 °C than at 25 °C. Reaction kinetics will be further constrained from mineralogy, elemental composition, and carbonate content of reaction products, enabling more precise quantification of the carbonation potential of the ultramafic/mafic rock types.
FT-Raman spectroscopic study of calcium-rich and magnesium-rich carbonate minerals.

PubMed

Edwards, Howell G M; Villar, Susana E Jorge; Jehlicka, Jan; Munshi, Tasnim

2005-08-01

Calcium and magnesium carbonates are important minerals found in sedimentary environments. Although sandstones are the most common rock colonized by endolith organisms, the production of calcium and magnesium carbonates is important in survival strategies of organisms and as a source for the removal of oxalate ions. Extremophile organisms in some situations may convert or destroy carbonates of calcium and magnesium, which gives important information about the conditions under which these organisms can survive. The identification on the surface of Mars of 'White Rock' formations, in Juventae Chasma or Sabaea Terra, as possibly carbonate rocks makes the study of these minerals a prerequisite of remote Martian exploration. Here, we show the protocol for the identification by Raman spectroscopy of different calcium and magnesium carbonates and we present a database of relevance in the search for life, extinct or extant, on Mars; this will be useful for the assessment of data obtained from remote, miniaturized Raman spectrometers now proposed for Mars exploration.
The effect of organic acids on wettability of sandstone and carbonate rocks

DOE Office of Scientific and Technical Information (OSTI.GOV)

Mwangi, Paulina; Brady, Patrick V.; Radonjic, Mileva

This paper examines the role of crude oil’s organic acid surface active compounds (SAC) in determining the reservoir wettability over a range of salinities and temperatures. To isolate the effects of individual SACs, this project used model oil mixtures of pure decane and single SACs to represent the oleic phase. Due to the large number of experiments in this study, we used wettability measurement method by the modified flotation technique (MFT) to produce fast, reliable, and quantitative results. The results showed that oil wetting by decane increased with temperature for carbonate rocks. Sandstones oil wetting showed little temperature dependency. Themore » presence of long-chained acids in decane increased oil wetting in sandstone and carbonate rocks as salinity was lowered, while the short-chained acid increased water wetting under the same conditions. The effect of organic acids on wettability was slightly enhanced with increasing temperature for all rock types.« less
The effect of organic acids on wettability of sandstone and carbonate rocks

DOE PAGES

Mwangi, Paulina; Brady, Patrick V.; Radonjic, Mileva; ...

2018-02-21

This paper examines the role of crude oil’s organic acid surface active compounds (SAC) in determining the reservoir wettability over a range of salinities and temperatures. To isolate the effects of individual SACs, this project used model oil mixtures of pure decane and single SACs to represent the oleic phase. Due to the large number of experiments in this study, we used wettability measurement method by the modified flotation technique (MFT) to produce fast, reliable, and quantitative results. The results showed that oil wetting by decane increased with temperature for carbonate rocks. Sandstones oil wetting showed little temperature dependency. Themore » presence of long-chained acids in decane increased oil wetting in sandstone and carbonate rocks as salinity was lowered, while the short-chained acid increased water wetting under the same conditions. The effect of organic acids on wettability was slightly enhanced with increasing temperature for all rock types.« less
Relative permeabilities of supercritical CO2 and brine in carbon sequestration by a two-phase lattice Boltzmann method

NASA Astrophysics Data System (ADS)

Xie, Jian.-Fei.; He, S.; Zu, Y. Q.; Lamy-Chappuis, B.; Yardley, B. W. D.

2017-08-01

In this paper, the migration of supercritical carbon dioxide (CO2) in realistic sandstone rocks under conditions of saline aquifers, with applications to the carbon geological storage, has been investigated by a two-phase lattice Boltzmann method (LBM). Firstly the digital images of sandstone rocks were reproduced utilizing the X-ray computed microtomography (micro-CT), and high resolutions (up to 2.5 μm) were applied to the pore-scale LBM simulations. For the sake of numerical stability, the digital images were "cleaned" by closing the dead holes and removing the suspended particles in sandstone rocks. In addition, the effect of chemical reactions occurred in the carbonation process on the permeability was taken into account. For the wetting brine and non-wetting supercritical CO2 flows, they were treated as the immiscible fluids and were driven by pressure gradients in sandstone rocks. Relative permeabilities of brine and supercritical CO2 in sandstone rocks were estimated. Particularly the dynamic saturation was applied to improve the reliability of the calculations of the relative permeabilities. Moreover, the effects of the viscosity ratio of the two immiscible fluids and the resolution of digital images on the relative permeability were systematically investigated.
Campanian-Maastrichtian phosphorites of Iraq

NASA Astrophysics Data System (ADS)

Al-Bassam, K. S.; Al-Dahan, A. A.; Jamil, A. K.

1983-08-01

Bedded marine sedimentary phosphate rocks of Campanian-Maastrichtian age are exposed in the Western Desert of Iraq, forming part of the Tethyan phosphate province. The studied phosphorites are found in three horizons within carbonate rocks; they are mostly pelletal in texture, associated with bone fragments and detrital quartz grains, and cemented by calcite or chert. The mineralogy of the phosphate is dominated by carbonate-fluorapatite. The phosphate and the associated carbonate rocks are relatively enriched with Cr, Ni, Cu, Zn, V, and organic matter. The apatite is enriched with isotopically light carbon and heavy sulfur. The mode of phosphorite formation seems to have included syngenetic deposition of phosphate under reducing, slightly alkaline conditions in shallow marine environment. Decomposition of organic phosphatic remnants appear to have been the local source of phosphorus enrichment. However, the major tectonic and paleogeographic development of the Tethys Sea during Upper Cretaceous have probably played an important role in providing suitable setting for large scale formation of phosphorite.
Comparative analysis of cyanobacteria inhabiting rocks with different light transmittance in the Mojave Desert: a Mars terrestrial analogue

NASA Astrophysics Data System (ADS)

Smith, Heather D.; Baqué, Mickael; Duncan, Andrew G.; Lloyd, Christopher R.; McKay, Christopher P.; Billi, Daniela

2014-05-01

The Mojave Desert has been long considered a suitable terrestrial analogue to Mars in many geological and astrobiological aspects. The Silver Lake region in the Mojave Desert hosts several different rock types (talc, marble, quartz, white carbonate and red-coated carbonate) colonized by hypoliths within a few kilometres. This provides an opportunity to investigate the effect of rock type on hypolithic colonization in a given environment. Transmission measurements from 300 to 800 nm showed that the transmission of blue and UVA varied between rock types. The wavelength at which the transmission fell to 1% of the transmission at 600 nm was 475 nm for white carbonate and quartz, 425 nm for red-coated carbonate and talc and 380 nm for marble. The comparative analysis of the cyanobacterial component of hypoliths under different rocks, as revealed by sequencing 16S rRNA gene clone libraries, showed no significant variation with rock type; hypoliths were dominated by phylotypes of the genus Chroococcidiopsis, although less abundant phylotypes of the genus Loriellopsis, Leptolyngbya and Scytonema occurred. The comparison of the confocal laser scanning microscopy-λ (CLSM-λ) scan analysis of the spectral emission of the photosynthetic pigments of Chroococcidiopsis in different rocks with the spectrum of isolated Chroococcidiopsis sp. 029, revealed a 10 nm red shift in the emission fingerprinting for quartz and carbonate and a 5 nm red shift for talc samples. This result reflects the versatility of Chroococcidiopsis in inhabiting dry niches with different light availability for photosynthesis.

A novel high-pressure vessel for simultaneous observations of seismic velocity and in situ CO2 distribution in a porous rock using a medical X-ray CT scanner

NASA Astrophysics Data System (ADS)

Jiang, Lanlan; Nishizawa, Osamu; Zhang, Yi; Park, Hyuck; Xue, Ziqiu

2016-12-01

Understanding the relationship between seismic wave velocity or attenuation and CO2 saturation is essential for CO2 storage in deep saline formations. In the present study, we describe a novel upright high-pressure vessel that is designed to keep a rock sample under reservoir conditions and simultaneously image the entire sample using a medical X-ray CT scanner. The pressure vessel is composed of low X-ray absorption materials: a carbon-fibre-enhanced polyetheretherketone (PEEK) cylinder and PEEK vessel closures supported by carbon-fibre-reinforced plastic (CFRP) joists. The temperature was controlled by a carbon-coated film heater and an aramid fibre thermal insulator. The assembled sample cell allows us to obtain high-resolution images of rock samples during CO2 drainage and brine imbibition under reservoir conditions. The rock sample was oriented vertical to the rotation axis of the CT scanner, and seismic wave paths were aligned parallel to the rotation axis to avoid shadows from the acoustic transducers. The reconstructed CO2 distribution images allow us to calculate the CO2 saturation in the first Fresnel zone along the ray path between transducers. A robust relationship between the seismic wave velocity or attenuation and the CO2 saturation in porous rock was obtained from experiments using this pressure vessel.
Geochemistry of arsenic in low sulfide-high carbonate coal waste rock, Elk Valley, British Columbia, Canada.

PubMed

Biswas, Ashis; Hendry, M Jim; Essilfie-Dughan, Joseph

2017-02-01

This study investigated the geochemistry of arsenic (As) in low sulfide-high carbonate coal waste rock of the Elk Valley, British Columbia, Canada. Its abundance and mineralogical associations in waste rock of different placement periods were determined in addition to its mobilization into porewater and rock-drain effluent. The mean (5.34mg/kg; 95% confidence interval: 4.95-5.73mg/kg) As concentration in the waste rock was typical of sedimentary rock. Electron microprobe and As K-edge X-ray absorption near-edge spectroscopic analyses showed the As is predominantly associated with primary pyrites in both source and freshly blasted waste rock. However, in aged waste rock the As is associated with both primary pyrites and secondary Fe oxyhydroxides. Oxidation of pyrite in waste rock dumps was reflected by the presence of high concentrations of SO 4 2- in porewater and oxidation rims of Fe oxyhydroxides around pyrite grains. Acid released from pyrite oxidation to Fe oxyhydroxides is neutralized by carbonate mineral dissolution that buffers the pH in the waste rock to circumneutral values. Adsorption of As onto secondary Fe oxyhydroxides provides an internal geochemical control on As release during pyrite oxidation and porewater flushing from the dump, resulting in the low As concentrations observed in porewater (median: 9.91μg/L) and rock-drain effluent (median: 0.31μg/L). Secondary Fe oxyhydroxides act as a long-term sink for As under present day hydrologic settings in waste rock dumps in the Elk Valley. Copyright © 2016 Elsevier B.V. All rights reserved.
Methods for assessing the polishing characteristics of coarse aggregates for use in pavement surface layers.

DOT National Transportation Integrated Search

2010-06-01

The predominant aggregate resources located in the western parts of Virginia are carbonate rocks. The mineral components of these rocks tend to be relatively soft and subject to abrasive wear under traffic that leads to a fairly rapid smoothing of th...
Spatial thermal radiometry contribution to the Massif Armoricain and the Massif Central (France) litho-structural study

NASA Technical Reports Server (NTRS)

Scanvic, J. Y. (Principal Investigator)

1980-01-01

Thermal zones delimited on HCMM images, by visual interpretation only, were correlated with geological units and carbonated rocks, granitic, and volcanic rocks were individualized. Rock signature is an evolutive parameter and some distinctions were made by addition of day, night and seasonal thermal image interpretation. This analysis also demonstrated that forest cover does not mask the underlying rocks thermal signature. Thermal anomalies were discovered. Geological targets were defined in the Paris Basin and the Montmarault granite.
Studying the impact of air/brine displacement on acoustic velocities in carbonates. El Amin Mokhtar and Sandra Vega

NASA Astrophysics Data System (ADS)

Mokhtar, E.; Vega, D.

2012-12-01

The impact of air/brine displacement on acoustic velocities of carbonate rocks is not fully comprehended yet. In order to improve our understanding of this effect, we conducted laboratory measurements of porosity and acoustic velocities (Vp and Vs) under both dry and brine saturated conditions at ambient pressure and temperature. The core plug samples in this study were collected from a hydrocarbon reservoir in the Middle East. A petrographic analysis was also performed on thin sections taken from the core plugs using a microscope and a digital camera. The aim of this analysis was to study depositional facies and the extent of diagenetic overprint that caused the observed variations in rock fabrics. Cross-plots were generated to analyze the trends of behavior between acoustic velocities and porosities taking into account the influence of different rock fabrics, in both dry and brine saturated samples. Acoustic velocities of brine saturated samples were higher than velocities of dry samples, as expected. However, their differences also respond to both, total porosity and carbonate rock fabrics. This result can be attributed to the different carbonate pore structures and rock frames formed during deposition and diagenesis. Similarly, the Vp/Vs ratio cross-plots display an increase in Vp/Vs ratios for the brine saturated samples compared to the dry ones. In conclusion, differences in acoustic velocities between dry and brine saturated carbonate rocks seem to be highly effected by porosity, rock fabric, and fluid content. This information can help to better understand the differences in acoustic response between gas and brine saturated zones in well logs and seismic.
The relationship between carbonate facies, volcanic rocks and plant remains in a late Palaeozoic lacustrine system (San Ignacio Fm, Frontal Cordillera, San Juan province, Argentina)

NASA Astrophysics Data System (ADS)

Busquets, P.; Méndez-Bedia, I.; Gallastegui, G.; Colombo, F.; Cardó, R.; Limarino, O.; Heredia, N.; Césari, S. N.

2013-07-01

The San Ignacio Fm, a late Palaeozoic foreland basin succession that crops out in the Frontal Cordillera (Argentinean Andes), contains lacustrine microbial carbonates and volcanic rocks. Modification by extensive pedogenic processes contributed to the massive aspect of the calcareous beds. Most of the volcanic deposits in the San Ignacio Fm consist of pyroclastic rocks and resedimented volcaniclastic deposits. Less frequent lava flows produced during effusive eruptions led to the generation of tabular layers of fine-grained, greenish or grey andesites, trachytes and dacites. Pyroclastic flow deposits correspond mainly to welded ignimbrites made up of former glassy pyroclasts devitrified to microcrystalline groundmass, scarce crystals of euhedral plagioclase, quartz and K-feldspar, opaque minerals, aggregates of fine-grained phyllosilicates and fiammes defining a bedding-parallel foliation generated by welding or diagenetic compaction. Widespread silicified and silica-permineralized plant remains and carbonate mud clasts are found, usually embedded within the ignimbrites. The carbonate sequences are underlain and overlain by volcanic rocks. The carbonate sequence bottoms are mostly gradational, while their tops are usually sharp. The lower part of the carbonate sequences is made up of mud which appear progressively, filling interstices in the top of the underlying volcanic rocks. They gradually become more abundant until they form the whole of the rock fabric. Carbonate on volcanic sandstones and pyroclastic deposits occur, with the nucleation of micritic carbonate and associated production of pyrite. Cyanobacteria, which formed the locus of mineral precipitation, were related with this nucleation. The growth of some of the algal mounds was halted by the progressive accumulation of volcanic ash particles, but in most cases the upper boundary is sharp and suddenly truncated by pyroclastic flows or volcanic avalanches. These pyroclastic flows partially destroyed the carbonate beds and palaeosols. Microbial carbonate clasts, silicified and silica-permineralized tree trunks, log stumps and other plant remains such as small branches and small roots inside pieces of wood (interpreted as fragments of nurse logs) are commonly found embedded within the ignimbrites. The study of the carbonate and volcanic rocks of the San Ignacio Fm allows the authors to propose a facies model that increases our understanding of lacustrine environments that developed in volcanic settings.
ASTER spectral sensitivity of carbonate rocks - Study in Sultanate of Oman

NASA Astrophysics Data System (ADS)

Rajendran, Sankaran; Nasir, Sobhi

2014-02-01

Remote sensing satellite data plays a vital role and capable in detecting minerals and discriminating rock types for explorations of mineral resources and geological studies. Study of spectral absorption characters of remotely sensed data are under consideration by the exploration and mining companies, and demonstrating the spectral absorption characters of carbonates on the cost-effective multispectral image (rather than the hyperspectral, Lidar image) for easy understanding of all geologists and exploration communities of carbonates is very much important. The present work is an integrated study and an outcome of recently published works on the economic important carbonate rocks, includes limestone, marl, listwaenites and carbonatites occurred in parts of the Sultanate of Oman. It demonstrates the spectral sensitivity of such rocks for simple interpretation over satellite data and describes and distinguishes them based on the absorptions of carbonate minerals in the spectral bands of advanced spaceborne thermal emission and reflection radiometer (ASTER) for mapping and exploration studies. The study results that the ASTER spectral band 8 discriminates the carbonate rocks due to the presence of predominantly occurred carbonate minerals; the ASTER band 5 distinguishes the limestones and marls (more hydroxyl clay minerals) from listwaenite (hydrothermally altered rock) due to the presence of altered minerals and the ASTER band 4 detects carbonatites (ultramafic intrusive alkaline rocks) which contain relatively more silicates. The study on the intensity of the total absorptions against the reflections of these rocks shows that the limestones and marls have low intensity in absorptions (and high reflection values) due to the presence of carbonate minerals (calcite and dolomite) occurred in different proportions. The listwaenites and carbonatites have high intensity of absorptions (low reflection values) due to the occurrence of Mn-oxide in listwaenites and carbonates in carbonatites apart the influence of major carbonate minerals that occurred predominantly in these rocks. The study of ASTER thermal infrared (TIR) spectral bands distinguished the marls have low emissivity of energy due to the presence of hydroxyl bearing alumina-silicate minerals from the other rocks such as limestones, listwaenites and carbonatites which have high emissivity due to the absence of hydroxyl bearing alumina-silicate minerals and the presence of carbonate minerals and carbonates. Further, the study demonstrates and confirms the spectral sensitivity of marls and carbonatites. Marls have high reflectivity in ASTER visible near infrared (VNIR) and shortwave infrared (SWIR) spectral bands and low emissivity of energy in ASTER TIR spectral bands due to the presence of hydroxyl bearing alumina-silicate minerals. Carbonatites have low reflectivity in ASTER VNIR-SWIR spectral bands and high emissivity in ASTER TIR spectral bands due to the absence of hydroxyl bearing alumina-silicate minerals and the presence of the carbonate minerals and carbonates. These have been discussed by providing the grey scale color image of 14 ASTER spectral bands of the study sites. The study is based on the interpretation of image spectra of multispectral image conducted to map such economic valuable carbonate rocks. It provides a simple methods and basic knowledge, which are of great help to the geology and exploration communities. It is recommended to the geologists, industrialists, exploration communities of carbonates and mine owners to take up the knowledge for economic exploration of such deposits. Further, the study has proved that the technique is time and cost effective in mapping of such deposits and can be used to the areas which have extremely rugged topography occurred in similar arid region, where difficult to do exhaustive sampling and not reachable for conventional geological mapping.
Evaluation of Five Sedimentary Rocks Other Than Salt for Geologic Repository Siting Purposes

DOE Office of Scientific and Technical Information (OSTI.GOV)

Croff, A.G.; Lomenick, T.F.; Lowrie, R.S.

The US Department of Energy (DOE), in order to increase the diversity of rock types under consideration by the geologic disposal program, initiated the Sedimary ROck Program (SERP), whose immediate objectiv eis to evaluate five types of secimdnary rock - sandstone, chalk, carbonate rocks (limestone and dolostone), anhydrock, and shale - to determine the potential for siting a geologic repository. The evaluation of these five rock types, together with the ongoing salt studies, effectively results in the consideration of all types of relatively impermeable sedimentary rock for repository purposes. The results of this evaluation are expressed in terms of amore » ranking of the five rock types with respect to their potential to serve as a geologic repository host rock. This comparative evaluation was conducted on a non-site-specific basis, by use of generic information together with rock evaluation criteria (RECs) derived from the DOE siting guidelines for geologic repositories (CFR 1984). An information base relevant to rock evaluation using these RECs was developed in hydrology, geochemistry, rock characteristics (rock occurrences, thermal response, rock mechanics), natural resources, and rock dissolution. Evaluation against postclosure and preclosure RECs yielded a ranking of the five subject rocks with respect to their potential as repository host rocks. Shale was determined to be the most preferred of the five rock types, with sandstone a distant second, the carbonate rocks and anhydrock a more distant third, and chalk a relatively close fourth.« less
Imaging Wellbore Cement Degradation by Carbon Dioxide under Geologic Sequestration Conditions Using X-ray Computed Microtomography

DOE Office of Scientific and Technical Information (OSTI.GOV)

Jung, Hun Bok; Jansik, Danielle; Um, Wooyong

2013-01-02

ABSTRACT: X-ray microtomography (XMT), a nondestructive three-dimensional imaging technique, was applied to demonstrate its capability to visualize the mineralogical alteration and microstructure changes in hydrated Portland cement exposed to carbon dioxide under geologic sequestration conditions. Steel coupons and basalt fragments were added to the cement paste in order to simulate cement-steel and cement-rock interfaces. XMT image analysis showed the changes of material density and porosity in the degradation front (density: 1.98 g/cm3, porosity: 40%) and the carbonated zone (density: 2.27 g/cm3, porosity: 23%) after reaction with CO2- saturated water for 5 months compared to unaltered cement (density: 2.15 g/cm3, porosity:more » 30%). Three-dimensional XMT imaging was capable of displaying spatially heterogeneous alteration in cement pores, calcium carbonate precipitation in cement cracks, and preferential cement alteration along the cement-steel and cement-rock interfaces. This result also indicates that the interface between cement and host rock or steel casing is likely more vulnerable to a CO2 attack than the cement matrix in a wellbore environment. It is shown here that XMT imaging can potentially provide a new insight into the physical and chemical degradation of wellbore cement by CO2 leakage.« less
Petrophysical, Lithological and Mineralogical Characteristics of the Shale Strata of the Volga- Ural Region

NASA Astrophysics Data System (ADS)

Morozov, Vladimir P.; Plotnikova, Irina N.; Pronin, Nikita V.; Nosova, Fidania F.; Pronina, Nailya R.

2014-05-01

The objects of the study are Upper Devonian carbonate rocks in the territory of South-Tatar arch and Melekess basin in the Volga- Urals region. We studied core material of Domanicoid facies from the sediments of Mendymski and Domanik horizons of middle substage of Frasnian stage of the Upper Devonian. Basic analytical research methods included the following: study of the composition, structural and textural features of the rocks, the structure of their voids, filter and reservoir properties and composition of the fluid. The complex research consisted of macroscopic description of the core material, optical microscopy analysis, radiographical analysis, thermal analysis, x-ray tomography, electron microscopy, gas-liquid chromatography, chromate-mass spectrometry, light hydrocarbons analysis using paraphase assay, adsorbed gases analysis, and thermal vacuum degassing method. In addition, we performed isotopic studies of hydrocarbons saturating shale rocks. Shale strata are mainly represented by carbonate-chert rocks. They consist mainly of calcite and quartz. The ratio of these rock-forming minerals varies widely - from 25 to 75 percent. Pyrite, muscovite, albite, and microcline are the most common inclusions. Calcareous and ferruginous dolomite (ankerite), as well as magnesian calcite are tracked down as secondary minerals. While performing the tests we found out that the walls of open fractures filled with oil are stacked by secondary dolomite, which should be considered as an indication moveable oil presence in the open-cut. Electron microscopy data indicate that all the studied samples have porosity - both carbonates and carbonate-siliceous rocks. Idiomorphism of the rock-forming grains and pores that are visible under a microscope bring us to that conclusion. The analysis of the images indicates that the type of reservoir is either porous or granular. The pores are distributed evenly in the volume of rock. Their size is very unstable and varies from 0.5 microns to 100 microns. The lowest value are observed in long carbonate-siliceous rocks, the highest values are found in carbonate rocks. The latter is caused by the fact that there is a very strong recrystallization of calcite and its dolomite substitution in carbonates. Open porosity ranges from 0.65 to 7.98 percent, average value is 4.1percent . Effective porosity has an average value of 0.44 percent, ranging from 0.22 to 1.97. Permeability varies from 0.043 to 1.49 mD, average value is 0,191 mD. Organic matter was found in all samples. Its content varies within the section. The fluctuation range of from 1.0 to 20 percent. The lowest content of carbonates is found in carbonates, while the highest is observed in carbonate-siliceous rocks with a high content of chalcedony. Average organic matter content is 5-7 percent. According to Rock-Eval studies of the core, the catagenetic maturity of organic matter corresponds to MK1 - MK2 degree. We found a connection between the type of organic matter and the composition of adsorbed gas. We also could see that the samples with humic organics present in their organic matter and can be characterized by a fair dominance of methane over other gases. There is a clear relationship between organic matter content and the intensity of the gas saturation of the rock. Organic matter is characteristic mainly of the most siliceous formations. In "pure" carbonates, which are represented by micro-layers with different capacities, OM is not observed at all or its content is quite low.
Acid neutralizing capacity and leachate results for igneous rocks, with associated carbon contents of derived soils, Animas River AML site, Silverton, Colorado

USGS Publications Warehouse

Yager, Douglas B.; Stanton, Mark R.; Choate, LaDonna M.; Burchell,

2009-01-01

Mine planning efforts have historically overlooked the possible acid neutralizing capacity (ANC) that local igneous rocks can provide to help neutralize acidmine drainage. As a result, limestone has been traditionally hauled to mine sites for use in neutralizing acid drainage. Local igneous rocks, when used as part of mine life-cycle planning and acid mitigation strategy, may reduce the need to transport limestone to mine sites because these rocks can contain acid neutralizing minerals. Igneous hydrothermal events often introduce moderately altered mineral assemblages peripheral to more intensely altered rocks that host metal-bearing veins and ore bodies. These less altered rocks can contain ANC minerals (calcite-chlorite-epidote) and are referred to as a propylitic assemblage. In addition, the carbon contents of soils in areas of new mining or those areas undergoing restoration have been historically unknown. Soil organic carbon is an important constituent to characterize as a soil recovery benchmark that can be referred to during mine cycle planning and restoration.
This study addresses the mineralogy, ANC, and leachate chemistry of propylitic volcanic rocks that host polymetallic mineralization in the Animas River watershed near the historical Silverton, Colorado, mining area. Acid titration tests on volcanic rocks containing calcite (2 – 20 wt %) and chlorite (6 – 25 wt %), have ANC ranging from 4 – 146 kg/ton CaCO₃ equivalence. Results from a 6-month duration, kinetic reaction vessel test containing layered pyritic mine waste and underlying ANC volcanic rock (saturated with deionized water) indicate that acid generating mine waste (pH 2.4) has not overwhelmed the ANC of propylitic volcanic rocks (pH 5.8). Sequential leachate laboratory experiments evaluated the concentration of metals liberated during leaching. Leachate concentrations of Cu-Zn-As-Pb for ANC volcanic rock are one-to-three orders of magnitude lower when compared to leached solution from mine waste used in the kinetic reaction vessel test. This finding suggests that mine waste and not ANC rock may generate the majority of leachable metals in a field scenario.
The organic carbon content of naturally reclaimed soils derived from weathering of propylitically-altered andesite was determined in catchments where ANC studies were initiated. Soils were found to have total carbon concentrations (TOC) that exceed global average soil TOC abundances by as much as 1.5 – 5 times. These data support an environmental management system involving use of ANC rocks as part of life-cycle mine planning to reduce post-mine closure acid mitigation measures. Carbon contents of undisturbed soils in mined catchments can possibly be used to validate post-reclamation success and help quantify carbon sequestration for CO₂ emission offset trading as carbon markets mature.
Integrated Experimental and Modeling Studies of Mineral Carbonation as a Mechanism for Permanent Carbon Sequestration in Mafic/Ultramafic Rocks

DOE Office of Scientific and Technical Information (OSTI.GOV)

Wang, Zhengrong; Qiu, Lin; Zhang, Shuang

2014-09-30

A program of laboratory experiments, modeling and fieldwork was carried out at Yale University, University of Maryland, and University of Hawai‘i, under a DOE Award (DE-FE0004375) to study mineral carbonation as a practical method of geologic carbon sequestration. Mineral carbonation, also called carbon mineralization, is the conversion of (fluid) carbon dioxide into (solid) carbonate minerals in rocks, by way of naturally occurring chemical reactions. Mafic and ultramafic rocks, such as volcanic basalt, are natural candidates for carbonation, because the magnesium and iron silicate minerals in these rocks react with brines of dissolved carbon dioxide to form carbonate minerals. By trappingmore » carbon dioxide (CO 2) underground as a constituent of solid rock, carbonation of natural basalt formations would be a secure method of sequestering CO 2 captured at power plants in efforts to mitigate climate change. Geochemical laboratory experiments at Yale, carried out in a batch reactor at 200°C and 150 bar (15 MPa), studied carbonation of the olivine mineral forsterite (Mg 2SiO 4) reacting with CO 2 brines in the form of sodium bicarbonate (NaHCO 3) solutions. The main carbonation product in these reactions is the carbonate mineral magnesite (MgCO 3). A series of 32 runs varied the reaction time, the reactive surface area of olivine grains and powders, the concentration of the reacting fluid, and the starting ratio of fluid to olivine mass. These experiments were the first to study the rate of olivine carbonation under passive conditions approaching equilibrium. The results show that, in a simple batch reaction, olivine carbonation is fastest during the first 24 hours and then slows significantly and even reverses. A natural measure of the extent of carbonation is a quantity called the carbonation fraction, which compares the amount of carbon removed from solution, during a run, to the maximum amount that could have been removed if the olivine initially present had fully dissolved and the cations released had subsequently precipitated in carbonate minerals. The carbonation fractions observed in batch experiments with olivine grains and powders varied significantly, from less than 0.01 (1%) to more than 0.5 (50%). Over time, the carbonation fractions reached an upper limit after about 24 to 72 hours of reaction, then stayed constant or decreased. The peak Final Scientific/Technical Report DE-FE0004275 | Mineral Carbonation | 4 coincided with the appearance of secondary magnesium-bearing silicate minerals, whose formation competes for magnesium ions in solution and can even promote conditions that dissolve magnesite. The highest carbonation fractions resulted from experiments with low ratios of concentrated solution to olivine, during which amorphous silica spheres or meshes formed, instead of secondary silicate minerals. The highest carbonation fractions appear to result from competing effects. Precipitation of silica layers on olivine reduces the reactive surface area and, thus, the rate of olivine dissolution (which ultimately limits the carbonation rate), but these same silica layers can also inhibit the formation of secondary silicate minerals that consume magnesite formed in earlier stages of carbonation. Simulation of these experiments with simple geochemical models using the software program EQ3/6 reproduces the general trends observed—especially the results for the carbonation fraction in short-run experiments. Although further experimentation and better models are needed, this study nevertheless provides a framework for understanding the optimal conditions for sequestering carbon dioxide by reacting CO 2-bearing fluids with rocks containing olivine minerals. A series of experiments at the Rock Physics Laboratory at the University of Maryland studied the carbonation process during deformation of thermally cracked olivine-rich rock samples (dunite) saturated with CO 2 brines of varying compositions. A goal of these geomechanical experiments was to see if flow and deformation processes, which accompany natural carbonation reactions in underground settings, work to enhance or inhibit the reactions. The experiments involved hydrostatic compaction, followed by deformation at a constant rate of strain. Sample permeability was monitored during the reactions. Comparison of the samples’ volume changes to their axial strains (shortening) during deformation indicates that samples reacted with CO 2-saturated brines accommodate more axial compaction, before the onset of dilation (a swelling that precedes rock failure), than samples reacted with distilled water. Analyses of the reacted samples with scanning electron microscope (SEM) images indicate, first, that dissolution of olivine occurring in the initial stages of carbonation can provide pathways to fluid flow that sustain the reaction, and, second, that carbonate minerals precipitated along existing fractures in the rocks may serve as asperities, or roughness on a crack’s surface that restricts its closure. Final Scientific/Technical Report DE-FE0004275 | Mineral Carbonation | 5 In a related study undertaken by one of the principal investigators as a spin-off of the main project, a simple model of (magnesite) crystal growth in the pore space of basalts undergoing carbonation was developed. The model suggests that, under a carefully controlled program of CO 2 injection, carbonate mineral growth can harden the rock formation against earthquakes that might otherwise be induced by the injection of large fluid volumes (Yarushina and Bercovici, 2013). The overall conclusion of the research project is that mineral carbonation of underground mafic and ultramafic rock formations is a viable candidate for long-term sequestration of man-made carbon dioxide. No results obtained during the project indicate that the method is inherently intractable in its implementation; moreover, enormous volumes of basalt near Earth’s surface are candidate locations for large-scale injection programs. The geochemical experiments do indicate, however, that there will be significant engineering challenges in maintaining high rates of carbonation, by delaying the onset of chemical conditions that promote formation of secondary silicate minerals and, therefore, slow down, or even reverse, the carbonation process. It remains an open question as to whether carbonation processes can be sustained for many years in an engineered system operating on a large scale—a scale capable of accommodating millions of tons of CO 2 annually. The development of realistic theoretical models that can systematically describe the combined effects of reactive flow, precipitation and geomechanical deformation is a major barrier to further understanding of the practical viability of mineral carbonation as large-scale method of carbon sequestration.« less
Methane seepage effects on biodiversity and biological traits of macrofauna inhabiting authigenic carbonates

NASA Astrophysics Data System (ADS)

Levin, Lisa A.; Mendoza, Guillermo F.; Grupe, Benjamin M.

2017-03-01

Authigenic carbonate rocks at methane seeps are recognized as hosting diverse and abundant invertebrate assemblages, with potential forcing from fluid seepage and hydrography. Mensurative studies of carbonate macrofauna (>0.3 mm) at Hydrate Ridge, OR revealed little effect of water depth and overlying oxygenation (at 600 m and 800 m) but a large influence of seepage activity on density, taxonomic composition, diversity, and biological traits (feeding, lifestyle, motility, size and calcification). Rocks exposed to active seepage had 3-4× higher total macrofaunal densities than under inactive conditions. Assemblages exhibited higher species richness and reduced evenness (greater dominance) under active seepage than inactive conditions, but no difference in H‧ or rarefaction diversity. Actively seeping sites were characterized by errant (motile), bacterial grazing, small- and medium-sized, heavily calcified species, whereas inactive sites exhibited a greater diversity of feeding modes and more burrowers, sessile, large and lightly calcified species. Active rocks supported more exogonid (Syllidae), ampharetid, and cirratulid polychaetes, provannid snails, pyropeltid limpets, nemerteans, and sponges; whereas inactive rocks supported higher densities of ophiuroids, isopods, gammarid amphipods, hydroids, Typosyllis (Syllidae) and tanaids. Transplant experiments, in which rocks were transferred between active and inactive sites at Hydrate Ridge North (600 m), revealed that assemblages respond within 13 months to increase or cessation of seepage, taking on the feeding, size and calcification characteristics of the background fauna at the new site. Lifestyles and motility patterns shifted more slowly as the sessile, attached species did not track seepage as quickly. Provannid snails and pyropeltid limpets rapidly colonized rocks transplanted to active sites and disappeared when transplanted to inactive sites. Given the known variability of fluid fluxes and rapid community response, a mosaic of communities changing in space and time is hypothesized to generate the relatively high species diversity at methane seeps.
Quantitative models for aggregate: some types and examples from Oklahoma carbonate rocks

USGS Publications Warehouse

Bliss, James D.

1999-01-01

Evaluation of data for three engineering variable--absorption, bulk specific gravity, and freeze-thaw durability (350 cycles)--was made for quarries in carbonate rocks in Oklahoma that supply aggregate. It was found that lower Palrozoic carbonate rocks (Cambrian through Devonian) are likely to make a better quality aggregate than upper Paleozoic (Mississippian to Permian) carbonate rocks. In addition, freeze-thaw durability can be forecast from absorption and is exemplary for lower Paleozoic carbonate rocks.
Geohydrologic reconnaissance of the upper Potomac River basin

USGS Publications Warehouse

Trainer, Frank W.; Watkins, Frank A.

1975-01-01

The upper Potomac River basin, in the central Appalachian region in Pennsylvania, Maryland, Virginia, and West Virginia, is a humid temperate region of diverse fractured rocks. Three geohydrologic terranes, which underlie large parts of the basin, are described in terms of their aquifer characteristics and of the magnitude and duration of their base runoff: (1) fractured rock having a thin regolith, (2) fractured rock having a thick regolith, and (3) carbonate rock. Crystalline rock in the mountainous part of the Blue Ridge province and shale with tight sandstone in the folded Appalachians are covered with thin regolith. Water is stored in and moves through fairly unmodified fractures. Average transmissivity (T) is estimated to be 150 feet squared per day, and average storage coefficient (S), 0.005. Base runoff declines rapidly from its high levels during spring and is poorly sustained during the summer season of high evapotranspiration. The rocks in this geohydrologic terrane are the least effective in the basin for the development of water supplies and as a source of dry-weather streamflow. Crystalline and sedimentary rocks in the Piedmont province and in the lowland part of the Blue Ridge province are covered with thick regolith. Water is stored in and moves through both the regolith and the underlying fractured rock. Estimated average values for aquifer characteristics are T, 200 feet squared per day, and S, 0.01. Base runoff is better sustained in this terrane than in the thin-regolith terrane and on the average .is about twice as great. Carbonate rock, in which fractures have been widened selectively by solution, especially near streams, has estimated average aquifer characteristics of T, 500 feet squared per day, and S, 0.03-0.04. This rock is the most effective in the basin in terms of water supply and base runoff. Where its fractures have not been widened by solution, the carbonate rock is a fractured-rock aquifer much like the noncarbonate rock. At low values the frequency of specific capacities of wells is much the same in all rocks in the basin, but high values of specific capacity are as much as 10 times more frequent in carbonate rock than in noncarbonate rock. Nearly all the large springs and high-capacity wells in the basin are in carbonate rock. Base runoff from the carbonate rock is better sustained during dry weather and on the average is about three times as great as base runoff from fractured rock having a thin regolith. The potential role of these water-bearing terranes in water management probably lies in the local development of large water supplies from the carbonate rock and in the possible manipulation of underground storage for such purposes as providing space for artificial recharge of ground water and providing ground water to be used for the augmentation of low streamflow. The chief water-quality problems in the basin--acidic mine-drainage water in the western part of the basin, local highly mineralized ground water, and the high nitrate content of ground water in some of the densely populated parts of the basin--would probably have little adverse affect on the use of ground water for low-flow augmentation.
Estimation of Carbon Sink in Surface Carbonate Rocks of Guangxi Province by Using Remote Sensing Images

NASA Astrophysics Data System (ADS)

Jia, B.; Zhou, G.; Wang, H.; Yue, T.; Huang, W.

2018-04-01

Studies of the imbalance of source sinks in the carbon cycle show that CO2 absorbed during rock weathering is part of the "miss carbon" of the global carbon cycle. The carbon sink contribution of carbonate rocks obviously plays a very important role in the absorption of atmospheric CO2. Estimation of carbon sinks in karst dynamic system of Guangxi province has great significance for further understanding of global karst carbon cycle and global climate research. This paper quotes the rock data from Tao Xiaodong's paper, which is obtained using RS and GIS techniques. At the same time, the dissolution rate model studied by Zhou Guoqing and others was used to estimate the dissolution rate of carbonate rocks in Guangxi Province. Finally, the CO2 content consumed by carbonate karstification in Guangxi Province was 1342910.447 t a-1. The results obtained are in the same order of magnitude as the CO2 content consumed by carbonate rock karstification in Guangxi Province calculated by Tao Xiaodong.
Inferences from Microfractures and Geochemistry in Dynamic Shale-CO2 Packed Bed Experiments

NASA Astrophysics Data System (ADS)

Radonjic, M.; Olabode, A.

2016-12-01

Subsurface storage of large volumes of carbondioxide (CO2) is expected to have long term rock-fluid interactions impact on reservoir and seal rocks properties. Caprocks, particularly sedimentary types, are the ultimate hydraulic barrier in carbon sequestration. The mineralogical components of sedimentary rocks are geochemically active under enormous earth stresses, which generate high pressure and temperature conditions. It has been postulated that in-situ mineralization can lead to flow impedance in natural fractures in the presence of favorable geochemical and thermodynamic conditions. This experimental modelling research investigated the impact of in-situ geochemical precipitation on conductivity of fractures. Geochemical analyses were performed on four different samples of shale rocks, effluent fluids and recovered precipitates both before and after CO2-brine flooding of crushed shale rocks at moderately high temperature and pressure conditions. The results showed that most significant diagenetic changes in shale rocks after flooding with CO2-brine, reflected in the effluent fluid with predominantly calcium based minerals dissolving and precipitating under experimental conditions. Major and trace elements in the effluent (using ICP-OES analysis) indicated that multiple geochemical reactions are occurring with almost all of the constituent minerals participating. The geochemical composition of precipitates recovered after the experiments showed diagenetic carbonates and opal as the main constituents. The bulk rock showed little changes in composition except for sharper and more refined peaks on XRD analysis, suggesting that a significant portion of the amorphous content of the rocks have been removed via dissolution by the slightly acid CO2-brine fluid that was injected. Micro-indentation results captured slight reduction in the hardness of the shale rocks and this reduction appeared dependent on diagenetic quartz content. It can be inferred that convective reactive transport of dissolved minerals are involved in nanoscale precipitation-dissolution processes in shale. This reactive transport of dissolved minerals can occlude micro-fracture flow paths, thereby improving shale caprock seal integrity with respect to leakage risk under CO2 sequestration conditions.
Pedogenic replacement of aluminosilicate grains by CaCO3 in Ustollic Haplargids, south-central Montana, U.S.A.

USGS Publications Warehouse

Reheis, M.C.

1988-01-01

A chronosequence of calcic soils formed on granitic glaciofluvial terrace deposits of Rock Creek and the Clarks Fork in south-central Montana shows progressive replacement of aluminosilicate parent-material grains by calcium-magnesium carbonate. The terraces range from late Pliocene to Holocene in age as dated by tephrochronology, correlation, and stream incision rates. Replacement is first seen in soils that are as old as 120,000 yr; the amount and degree of replacement increase in soils older than 120,000 yr along with the development of calcic horizons. Under the petrographic microscope, carbonate replacement of quartz, feldspars, and the groundmass of andesite grains in Rock Creek soils is shown by embayed grains, networks of carbonate along cracks and between parts of polycrystalline grains and optically aligned grain fragments within carbonate masses. Microprobe data suggest that silica is released by replacement because it is absent from carbonate-filled spaces and is depleted in corrosion pits. Little microscopic evidence exists to support displacement of framework grains by carbonate because fragments of a single grain are rarely rotated out of optical alignment. In the calcic soils of Rock Creek, K-fabric (grains floating in a carbonate matrix) may form by both replacement and displacement. ?? 1988.
Carbonation of Rock Minerals by Supercritical Carbon Dioxide at 250 degrees C.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Sugama, T.; Ecker, L.; Butcher, T.

2010-06-01

Wet powder-samples of five rock minerals, granite, albite, hornblende, diorite, and biotite mica, were exposed in supercritical carbon dioxide (scCO2) for 3 days at 250 C under 17.23 MPa pressure, and then the susceptibility of the various crystalline phases present in these mineral structures to reactions with hot scCO2 was investigated by XRD and FT-IR. The anorthite present in diorite was identified as the most vulnerable phase to carbonation. In contrast, biotite displayed a great resistance, although its phase was transformed hydrothermally to sanidine and quartz. Granite comprised of two phases, anorthoclase-type albite and quartz. The carbonation of former phasemore » led to the formation of amorphous sodium and potassium carbonates coexisting with the clay-like by-products of the carbonation reaction. The reactivity of quartz to scCO2 was minimal, if any. Among these rock minerals, only hornblende formed crystalline carbonation products, such as calcite and magnesite after exposure, reflecting the likelihood of an increase in its volume. Based upon the feldspar ternary diagram, the carbonation rate of various different minerals in the plagioclase feldspar family depended primarily on the amount of anorthite. On the other hand, alkali feldspar minerals involving anorthoclase-type albite and sanidine had a lower reactivity with scCO2, compared with that of plagioclase feldspar minerals.« less
Kinetics of carbonate dissolution in CO2-saturated aqueous system at reservoir conditions

NASA Astrophysics Data System (ADS)

Peng, Cheng; Crawshaw, John P.; Maitland, Geoffrey; Trusler, J. P. Martin

2014-05-01

In recent years, carbon capture and storage (CCS) has emerged as a key technology for limiting anthropogenic CO2 emissions while allowing the continued utilisation of fossil fuels. The most promising geological storage sites are deep saline aquifers because the capacity, integrity and injection economics are most favourable, and the environmental impact can be minimal. Many rock-fluid chemical reactions are known to occur both during and after CO2 injection in saline aquifers. The importance of rock-fluid reactions in the (CO2 + H2O) system can be understood in terms of their impact on the integrity and stability of both the formation rocks and cap rocks. The chemical interactions between CO2-acidified brines and the reservoir minerals can influence the porosity and permeability of the formations, resulting in changes in the transport processes occurring during CO2 storage. Since carbonate minerals are abundant in sedimentary rocks, one of the requirements to safely implement CO2 storage in saline aquifers is to characterise the reactivity of carbonate minerals in aqueous solutions at reservoir conditions. In this work, we reported measurements of the intrinsic rate of carbonate dissolution in CO2-saturated water under high-temperature high-pressure reservoir conditions extending up to 373 K and 14 MPa. The rate of carbonate dissolution in CO2-free HCl(aq) was also measured at ambient pressure at temperatures up to 353 K. Various pure minerals and reservoir rocks were investigated in this study, including single-crystals of calcite and magnesite, and samples of dolomite, chalks and sandstones. A specially-designed batch reactor system, implementing the rotating disc technique, was used to obtain the intrinsic reaction rate at the solid/liquid interface, free of mass transfer effects. The effective area and mineralogy of the exposed surface was determined by a combination of surface characterisation techniques including XRD, SEM, EDX and optical microscopy. The results of the study indicate that the rotating disc technique can allow accurate measurement of the carbonate dissolution rate under surface-reaction-controlled conditions, and that the carbonate dissolution rate typically increases with the increase of temperature, CO2 partial pressure and solution acidity. The study shows that the dissolution of carbonate in CO2-free acidic solutions can be described as a first order heterogeneous reaction; however, this model is not sufficient to describe the reaction kinetics of carbonate minerals in the (CO2 + H2O) system, particularly for high reactivity carbonates, such as calcite, at reservoir conditions. For these systems, both pH and the activity of CO2(aq) influence the dissolution rate. Based on the experimental results, kinetic models have been developed and parameterised to describe the dissolution of different carbonate minerals. The results of this study should facilitate more rigorous modelling of mineral dissolution in deep saline aquifers used for CO2 storage. We gratefully acknowledge the funding of QCCSRC provided jointly by Qatar Petroleum, Shell, and the Qatar Science & Technology Park. Keywords: Carbon Dioxide, Carbonate, High Pressure, High Temperature, Reaction Kinetics.

The role of major forest fires on rock physical decay in a Mediterranean environment

NASA Astrophysics Data System (ADS)

Shtober-Zisu, Nurit; Tessler, Naama; Tsatskin, Alexander; Greenbaum, Noam

2017-04-01

Massive destruction of carbonate rocks occurred on the slopes of Mt. Carmel (Israel), during a severe forest fire in 2010. The bedrock surfaces exhibited extensive exfoliation into flakes and spalls covering up to 80%-100% of the exposed rocks; detached boulders were totally fractured or disintegrated. The fire affected six carbonate units—various types of chalk, limestone, and dolomite. The burned flakes show a consistent tendency towards flatness, in all lithologies, as 85%-95% of the flakes were detached in the form of blades, plates, and slabs. The extent of the physical disruption depends on rock composition: the most severe response was found in the chalk formations which are covered by calcrete (Nari crusts). These rocks reacted by extreme exfoliation, at an average depth of 7.7 to 9.6 cm and a maximum depth of 20 cm. Scorched and blackened faces under the upper layer of spalls provide strong evidence that chalk breakdown took place at an early stage of the fire. The extreme response of the chalks can be explained by the laminar structure of the Nari, which served as planes of weakness for the rock destruction. Three years after the fire, the rocks continue to exfoliate and break down internally. As the harder surface of the Nari was removed, the more brittle underlying chalk is exposed to erosion. These flakes seem to play an important role in reforming the soil after the fire, especially by increasing the coarse particles percentage. These, in spite of the absence of vegetation cover, improve soil infiltration and percolation rates and cause long-term changes to the hydrological regime. It is difficult to estimate the frequency of high-intensity fires in the Carmel region over the past 2-3 million years, as well as the extension and density of the vegetation. It is even harder to assess the frequency of fires (and the destruction) of a single rock outcrop. Our findings show that rock outcrop may lose even 20 cm of its thickness in a single fire. This value, if accounted to the long run, can be responsible for a high percentage of the total denudation rate and therefore, in the mountainous carbonate slopes of the Mediterranean region, wildland fires may serve as extremely important factors in landscape evolution (Shtober-Zisu et al., 2015). Shtober-Zisu, N., Tessler, N., Tsatskin, A., & Greenbaum, N. (2015). Accelerated weathering of carbonate rocks following the 2010 wildfire on Mount Carmel, Israel. International Journal of Wildland Fire, 24(8): 1154-1167.
Reproducing early Martian atmospheric carbon dioxide partial pressure by modeling the formation of Mg-Fe-Ca carbonate identified in the Comanche rock outcrops on Mars

NASA Astrophysics Data System (ADS)

Berk, Wolfgang; Fu, Yunjiao; Ilger, Jan-Michael

2012-10-01

The well defined composition of the Comanche rock's carbonate (Magnesite0.62Siderite0.25Calcite0.11Rhodochrosite0.02) and its host rock's composition, dominated by Mg-rich olivine, enable us to reproduce the atmospheric CO2partial pressure that may have triggered the formation of these carbonates. Hydrogeochemical one-dimensional transport modeling reveals that similar aqueous rock alteration conditions (including CO2partial pressure) may have led to the formation of Mg-Fe-Ca carbonate identified in the Comanche rock outcrops (Gusev Crater) and also in the ultramafic rocks exposed in the Nili Fossae region. Hydrogeochemical conditions enabling the formation of Mg-rich solid solution carbonate result from equilibrium species distributions involving (1) ultramafic rocks (ca. 32 wt% olivine; Fo0.72Fa0.28), (2) pure water, and (3) CO2partial pressures of ca. 0.5 to 2.0 bar at water-to-rock ratios of ca. 500 molH2O mol-1rock and ca. 5°C (278 K). Our modeled carbonate composition (Magnesite0.64Siderite0.28Calcite0.08) matches the measured composition of carbonates preserved in the Comanche rocks. Considerably different carbonate compositions are achieved at (1) higher temperature (85°C), (2) water-to-rock ratios considerably higher and lower than 500 mol mol-1 and (3) CO2partial pressures differing from 1.0 bar in the model set up. The Comanche rocks, hosting the carbonate, may have been subjected to long-lasting (>104 to 105 years) aqueous alteration processes triggered by atmospheric CO2partial pressures of ca. 1.0 bar at low temperature. Their outcrop may represent a fragment of the upper layers of an altered olivine-rich rock column, which is characterized by newly formed Mg-Fe-Ca solid solution carbonate, and phyllosilicate-rich alteration assemblages within deeper (unexposed) units.
Effect of Palagonite Dust Deposition on the Automated Detection of Carbonate Vis/NIR Spectra

NASA Technical Reports Server (NTRS)

Gilmore, Martha S.; Merrill, Matthew D.; Castano, Rebecca; Bornstein, Benjamin; Greenwood, James

2004-01-01

Currently Mars missions can collect more data than can be returned. Future rovers of increased mission lifetime will benefit from onboard autonomous data processing systems to guide the selection, measurement and return of scientifically important data. One approach is to train a neural net to recognize spectral reflectance characteristics of minerals of interest. We have developed a carbonate detector using a neural net algorithm trained on 10,000 synthetic Vis/NIR (350-2500 nm) spectra. The detector was able to correctly identify carbonates in the spectra of 30 carbonate and noncarbonate field samples with 100% success. However, Martian dust coatings strongly affect the spectral characteristics of surface rocks potentially masking the underlying substrate rock. In this experiment, we measure Vis/NIR spectra of calcite coated with different thicknesses of palagonite dust and evaluate the performance of the carbonate detector.
Studies of geology and hydrology in the Basin and Range Province, Southwestern United States, for isolation of high-level radioactive waste - Characterization of the Bonneville region, Utah and Nevada

USGS Publications Warehouse

Bedinger, M.S.; Sargent, K.A.; Langer, William H.

1990-01-01

The Bonneville region of the Basin and Range province in westcentral Utah and adjacent Nevada includes several basins lying south of the Great Salt Lake Desert. Physiographically, the region consists of linear, north-trending mountain ranges separated by valleys, many of which are closed basins underlain by thick sequences of fill. Surface drainage of open basins and ground-water flow is to the Great Salt Lake Desert. In structure and composition the ranges are faulted Paleozoic rocks, locally intruded by Mesozoic and Tertiary plugs and stocks. In the southern and northeastern parts of the region, volcanic rocks are widespread and form large parts of some mountain ranges. The Paleozoic sedimentary rocks include great thicknesses of carbonate rocks which compose a significant aquifer in the regionMedia considered to have potential for isolation of high-level radioactive waste in the region include intrusive rocks, such as granite; ash-flow tuff; and basalt and basaltic andesite lava flows. These rock types, basin fill, and possibly other rock types, may have potential as host media in the unsaturated zone. Quaternary tectonism in the region is evidenced by seismic activity, local areas of above-normal geothermal heat flow, Quaternary faulting, late Cenozoic volcanic activity, and active vertical crustal movement. The Bonneville region is part of a large ground-water flow system that is integrated partly through basin-fill deposits, but largely through an underlying carbonate-rock sequence. The region includes: (1) several topographically closed basins with virtually no local surface discharge that are drained by the underlying carbonate-rock aquifer; (2) closed basins with local surface discharge by evapotranspiration; and (3) basins open to the Great Salt Lake Desert that discharge by groundwater underflow and evapotranspiration. The carbonate-rock aquifer discharges to large springs in the Desert and in basins tributary to the Desert. The climate is arid to semiarid with the greatest precipitation in the mountain ranges. Most recharge probably occurs by infiltration of runoff as it leaves the mountains, although some recharge probably occurs directly to the carbonate rocks in the mountain areas. The concentration of dissolved solids in ground water is generally less than 500 milligrams per liter. Dissolved-solids concentrations increase in the Great Salt Lake Desert and in major valleys adjoining the Desert. The predominant chemical constituents in ground water are calcium, magnesium, and sodium bicarbonate. Chloride-type water is associated with the higher dissolved-solids content of water in and near the Great Salt Lake Desert. The majority of the mineral occurrences containing base- and precious-metal deposits in the Bonneville region are of Tertiary age. Fluorspar is the primary industrial mineral. Coal, oil, and gas have not been produced in significant amounts.
Bicarbonate content of groundwater in carbonate rock in eastern North America

USGS Publications Warehouse

Trainer, F.W.; Heath, R.C.

1976-01-01

In carbonate-rock terrane the most effective solution occurs where soil and vegetative cover facilitate biogenic production and storage of CO2 in the soil until part of it is carried downward in percolating water. Bicarbonate data for groundwater in eastern North America are examined in the light of these conditions, of the CO2 content of soil gas, and of the timing of groundwater recharge relative to seasonal changes in soil temperature. There appears to be no well-marked relation between latitude and bicarbonate content of groundwater in this region. Interplay of all the factors listed above, and of lithology and soil types, is evidently such that under optimum conditions the amount of solution of carbonate rock is roughly comparable, per unit of groundwater recharge, over the region from Ohio to Florida (and, perhaps, to Puerto Rico and Yucatan). Relatively low HCO3 concentrations observed in much of the southern United States are attributed to low production and storage of CO2 in sandy soil that is poor in organic matter. On the other hand, concentrations observed in Ontario, New York and Michigan are markedly higher than is to be expected from interrelations of the factors considered. These high values, apparently anomalous, are attributed in part to solution of granular glacial drift derived largely from carbonate rock. ?? 1976.
Biologically mediated isotope fractionations - Biochemistry, geochemical significance and preservation in the earth's oldest sediments

NASA Technical Reports Server (NTRS)

Schidlowski, M.

1983-01-01

Preferential metabolization of isotopically light carbon and sulfur has resulted in a fractionation of the stable isotopes of these elements on a global scale, with the light species (C-12, S-32) markedly concentrated in biogenic materials. Since the biological effects are basically retained when carbon and sulfur are incorporated in sediments, the respective fractionations are propagated into the rock section of the geochemical cycle, this having consequently caused a characteristic bipartition of both elements between 'light' and 'heavy' crustal reservoirs. Preservation of the biological isotope effects in sedimentary rocks makes it possible to trace the underlying biochemical processes back over most of the geological record. According to the available evidence, biological (autotrophic) carbon fixation arose prior to 3.5(if not 3.8) billion years ago, while the emergence of dissimilatory sulfate reduction antedates the appearance of the oldest presumably bacteriogenic sulfur isotope patterns in rocks between 2.7 and 2.8 billion years old. Hence, biological control of the terrestrial carbon and sulfur cycles has been established very early in the earth's history.
Enhanced Weathering Strategies for Stabilizing Climate and Averting Ocean Acidification

NASA Technical Reports Server (NTRS)

Taylor, Lyla L.; Quirk, Joe; Thorley, Rachel M. S.; Kharecha, Pushker A.; Hansen, James; Ridgwell, Andy; Lomas, Mark R.; Banwart, Steve A.; Beerling, David J.

2015-01-01

Chemical breakdown of rocks, weathering, is an important but very slow part of the carbon cycle that ultimately leads to CO2 being locked up in carbonates on the ocean floor. Artificial acceleration of this carbon sink via distribution of pulverized silicate rocks across terrestrial landscapes may help offset anthropogenic CO2 emissions. We show that idealized enhanced weathering scenarios over less than a third of tropical land could cause significant drawdown of atmospheric CO2 and ameliorate ocean acidification by 2100. Global carbon cycle modelling driven by ensemble Representative Concentration Pathway (RCP) projections of twenty-first-century climate change (RCP8.5, business-as-usual; RCP4.5, medium-level mitigation) indicates that enhanced weathering could lower atmospheric CO2 by 30-300 ppm by 2100, depending mainly on silicate rock application rate (1 kg or 5 kg m(exp -2) yr (exp -1)) and composition. At the higher application rate, end-of-century ocean acidification is reversed under RCP4.5 and reduced by about two-thirds under RCP8.5. Additionally, surface ocean aragonite saturation state, a key control on coral calcification rates, is maintained above 3.5 throughout the low latitudes, thereby helping maintain the viability of tropical coral reef ecosystems. However, we highlight major issues of cost, social acceptability, and potential unanticipated consequences that will limit utilization and emphasize the need for urgent efforts to phase down fossil fuel emissions.
Enhanced weathering strategies for stabilizing climate and averting ocean acidification

NASA Astrophysics Data System (ADS)

Taylor, Lyla L.; Quirk, Joe; Thorley, Rachel M. S.; Kharecha, Pushker A.; Hansen, James; Ridgwell, Andy; Lomas, Mark R.; Banwart, Steve A.; Beerling, David J.

2016-04-01

Chemical breakdown of rocks, weathering, is an important but very slow part of the carbon cycle that ultimately leads to CO2 being locked up in carbonates on the ocean floor. Artificial acceleration of this carbon sink via distribution of pulverized silicate rocks across terrestrial landscapes may help offset anthropogenic CO2 emissions. We show that idealized enhanced weathering scenarios over less than a third of tropical land could cause significant drawdown of atmospheric CO2 and ameliorate ocean acidification by 2100. Global carbon cycle modelling driven by ensemble Representative Concentration Pathway (RCP) projections of twenty-first-century climate change (RCP8.5, business-as-usual; RCP4.5, medium-level mitigation) indicates that enhanced weathering could lower atmospheric CO2 by 30-300 ppm by 2100, depending mainly on silicate rock application rate (1 kg or 5 kg m-2 yr-1) and composition. At the higher application rate, end-of-century ocean acidification is reversed under RCP4.5 and reduced by about two-thirds under RCP8.5. Additionally, surface ocean aragonite saturation state, a key control on coral calcification rates, is maintained above 3.5 throughout the low latitudes, thereby helping maintain the viability of tropical coral reef ecosystems. However, we highlight major issues of cost, social acceptability, and potential unanticipated consequences that will limit utilization and emphasize the need for urgent efforts to phase down fossil fuel emissions.
Enhanced Weathering Strategies for Stabilizing Climate and Averting Ocean Acidification - Supplementary Information

NASA Technical Reports Server (NTRS)

Taylor, Lyla L.; Quirk, Joe; Thorley, Rachel M. S.; Kharecha, Pushker A.; Hansen, James; Ridgwell, Andy; Lomas, Mark R.; Banwart, Steve A.; Beerling, David J.

2015-01-01

Chemical breakdown of rocks, weathering, is an important but very slow part of the carbon cycle that ultimately leads to CO2 being locked up in carbonates on the ocean floor. Artificial acceleration of this carbon sink via distribution of pulverized silicate rocks across terrestrial landscapes may help offset anthropogenic CO2 emissions. We show that idealized enhanced weathering scenarios over less than a third of tropical land could cause significant drawdown of atmospheric CO2 and ameliorate ocean acidification by 2100. Global carbon cycle modelling driven by ensemble Representative Concentration Pathway (RCP) projections of twenty-first-century climate change (RCP8.5, business-as-usual; RCP4.5, medium-level mitigation) indicates that enhanced weathering could lower atmospheric CO2 by 30-300 ppm by 2100, depending mainly on silicate rock application rate (1 kg or 5 kg m(exp. -2) yr (exp -1)) and composition. At the higher application rate, end-of-century ocean acidification is reversed under RCP4.5 and reduced by about two-thirds under RCP8.5. Additionally, surface ocean aragonite saturation state, a key control on coral calcification rates, is maintained above 3.5 throughout the low latitudes, thereby helping maintain the viability of tropical coral reef ecosystems. However, we highlight major issues of cost, social acceptability, and potential unanticipated consequences that will limit utilization and emphasize the need for urgent efforts to phase down fossil fuel emissions.
Accelerated weathering of carbonate rocks following the 2010 forest wildfire on Mt. Carmel, Israel

NASA Astrophysics Data System (ADS)

Shtober-Zisu, Nurit; Tessler, Naama; Tsatskin, Alexander; Greenbaum, Noam

2015-04-01

Massive destruction of carbonate rocks occurred on the slopes of Mt. Carmel, during the severe forest fire in 2010. The bedrock surfaces exhibited extensive exfoliation into flakes and spalls covering up to 80%-100% of the exposed rocks; detached boulders were totally fractured or disintegrated. The fire affected six carbonate units -- various types of chalk, limestone, and dolomite. The burned flakes show a consistent tendency towards flatness, in all lithologies, as 85%-95% of the flakes were detached in the form of blades, plates, and slabs. The effects of the fire depend to a large extent on the rocks' physical properties and vary with lithology: the most severe response was found in the chalk formations which are covered by calcrete (Nari crusts). These rocks reacted by extreme exfoliation, at an average depth of 7.7 to 9.6 cm and a maximum depth of 20 cm. The flakes formed in chalk were thicker, longer, and wider than those of limestone or dolomite formations. Moreover, the chalk outcrops were exfoliated in a laminar structure, one above the other, to a depth of 10 cm and more. Their shape also tended to be blockier or rod-like. In contrast, the limestone flakes were the thinnest, with 99% of them shaped like blades and plates. Scorched and blackened faces under the upper layer of spalls provided strong evidence that chalk breakdown took place at an early stage of the fire. The extreme response of the chalks can be explained by the laminar structure of the Nari, which served as planes of weakness for the rock destruction. Three years after the fire, the rocks continue to exfoliate and break down internally. As the harder surface of the Nari was removed, the more brittle underlying chalk is exposed to erosion. If fires can obliterate boulders in a single wildfire event, it follows that wildfires may serve as limiting agents in the geomorphic evolution of slopes. However, it is difficult to estimate the frequency of high-intensity fires in the Carmel region over the past 2-3 million years. It is even harder to assess the frequency of fires (and the destruction) of a single rock outcrop. Our findings show that rock outcrop may lose even 20 cm of its thickness in a single fire. This value, if accounted to the long run, can be responsible for a high percentage of the total denudation rate and therefore, in the mountainous carbonate slopes of the Mediterranean region, wildland fires may serve as extremely important factors in landscape evolution.
CO 2-induced chemo-mechanical alteration in reservoir rocks assessed via batch reaction experiments and scratch testing

DOE Office of Scientific and Technical Information (OSTI.GOV)

Aman, Michael; Espinoza, D. Nicolas; Ilgen, Anastasia G.

Here, the injection of carbon dioxide (CO 2) into geological formations results in a chemical re-equilibration between the mineral assemblage and the pore fluid, with ensuing mineral dissolution and re-precipitation. Hence, target rock formations may exhibit changes of mechanical and petrophysical properties due to CO 2 exposure. We conducted batch reaction experiments with Entrada Sandstone and Summerville Siltstone exposed to de-ionized water and synthetic brine under reservoir pressure (9–10 MPa) and temperature (80°C) for up to four weeks. Samples originate from the Crystal Geyser field site, where a naturally occurring CO 2 seepage alters portions of these geologic formations. Wemore » conducted micro-scratch tests on rock samples without alteration, altered under laboratory conditions, and naturally altered over geologic time. Scratch toughness and hardness decrease as a function of exposure time and water salinity up to 52% in the case of Entrada and 87% in the case of Summerville after CO 2-induced alteration in the laboratory. Imaging of altered cores with SEM-EDS and X-ray microCT methods show dissolution of carbonate and silica cements and matrix accompanied by minor dissolution of Fe-oxides, clays, and other silicates. Parallel experiments using powdered samples confirm that dissolution of carbonate and silica are the primary reactions. The batch reaction experiments in the autoclave utilize a high fluid to rock volume ratio and represent an end member of possible alteration associated with CO 2 storage systems. These types of tests serve as a pre-screening tool to identify the susceptibility of rock facies to CO 2-related chemical-mechanical alteration during long-term CO 2 storage.« less
CO 2-induced chemo-mechanical alteration in reservoir rocks assessed via batch reaction experiments and scratch testing

DOE PAGES

Aman, Michael; Espinoza, D. Nicolas; Ilgen, Anastasia G.; ...

2017-09-22

Here, the injection of carbon dioxide (CO 2) into geological formations results in a chemical re-equilibration between the mineral assemblage and the pore fluid, with ensuing mineral dissolution and re-precipitation. Hence, target rock formations may exhibit changes of mechanical and petrophysical properties due to CO 2 exposure. We conducted batch reaction experiments with Entrada Sandstone and Summerville Siltstone exposed to de-ionized water and synthetic brine under reservoir pressure (9–10 MPa) and temperature (80°C) for up to four weeks. Samples originate from the Crystal Geyser field site, where a naturally occurring CO 2 seepage alters portions of these geologic formations. Wemore » conducted micro-scratch tests on rock samples without alteration, altered under laboratory conditions, and naturally altered over geologic time. Scratch toughness and hardness decrease as a function of exposure time and water salinity up to 52% in the case of Entrada and 87% in the case of Summerville after CO 2-induced alteration in the laboratory. Imaging of altered cores with SEM-EDS and X-ray microCT methods show dissolution of carbonate and silica cements and matrix accompanied by minor dissolution of Fe-oxides, clays, and other silicates. Parallel experiments using powdered samples confirm that dissolution of carbonate and silica are the primary reactions. The batch reaction experiments in the autoclave utilize a high fluid to rock volume ratio and represent an end member of possible alteration associated with CO 2 storage systems. These types of tests serve as a pre-screening tool to identify the susceptibility of rock facies to CO 2-related chemical-mechanical alteration during long-term CO 2 storage.« less
Complex resistivity spectra in relation to multiscale pore geometry in carbonates and mixed-siliciclastic rocks

NASA Astrophysics Data System (ADS)

Norbisrath, Jan Henrik

Carbonate rocks are known to have complex and heterogeneous pore structures, which result from their biogenic origin and strong affinity for diagenetic processes that change their pore structure after burial. The combination of sheer endless variations of precursor biogenic material, depositional environments, and diagenetic effects results in rocks that are interesting to study but intricate to understand. Many schemes to categorize the diversity of carbonate rocks are in use today; most are based on the macropore structure and qualitative thin-section analysis. Many studies, however, acknowledge that micropores have a significant influence on the macroscopic petrophysical rock properties, which are essential to determine reservoir quality. Micropores are, by definition, smaller than the thickness of a thin-section (< 30 microm) and hence cannot be quantified with conventional methods. For their analysis, scanning electron microscopy (SEM) is the logical next step. The challenge is that mechanical polishing methods produce excessive surface roughness at micron scale; the resulting surfaces are not suited for quantification of micropores. Advances in broad-ion-beam (BIB) milling enable preparation of nanometer-precision 2D sections that are suited for quantitative analysis with the SEM. To accomplish the objective of accurate quantification of carbonate micropores, part one of this dissertation employs the BIB-SEM technique on a variety of carbonate rock samples and finds four major carbonate microporosity types: (1) small intercrystalline, (2) large inter-crystalline, (3) intercement, and (4) micromoldic. Each microporosity type shows a distinct capacity to conduct electrical charge, which largely controls the magnitude and range of cementation factors (m) in rocks with such microporosity type. The BIB-SEM method is also used on a dataset of mixed carbonate-siliciclastic (mudrock) samples with high kerogen and pyrite content. Results show that the nanopore geometry here has little influence on cementation factors, and instead porosity is the main control on m in mudrocks. Cementation factors are crucial for estimates of oil-in-place and water saturation in a wireline application, and a slight change of (assumed) cementation factor can change the interpreter's evaluation from dry hole to discovery. Therefore, accurate determination of cementation factors is a critical task in formation evaluation, similar to accurate estimates of permeability. To achieve this goal, this dissertation utilizes a new approach of using complex resistivity spectra (CRS) to assess the pore geometry and its resulting electrical and fluid flow properties. Specifically, frequency dispersion of complex resistivity in the kHz range is used as input for a new model to predict cementation factor and permeability in a wide variety of core plug samples. The underlying concept that relates CRS to flow properties is that both are related to pore geometry. CRS are linked to pore geometry by interfacial polarization effects at the fluid-rock boundary that control the phase and amplitude shift of an applied alternating current. Larger interfacial area results in higher phase shifts, but also indicates a more intricate pore structure that often results in lower permeability and higher cementation factors. The findings from this dissertation imply that (1) the CRS prediction method greatly improves estimates of cementation factors and permeability in carbonate, dolomite, and mixed siliciclastic rocks, (2) there are at least four distinct microporosity types in carbonate rocks, which have great impact on cementation factors and permeability, (3) nanopore geometry has a small impact on electrical flow properties in mudrocks where the main control on cementation factors is porosity, and (4) all sedimentary limestone and mixed carbonate-siliciclastic rocks have power law pore size distributions.
Rock Magnetic Properties of Remagnetised Devonian and Carboniferous Carbonate and Clastic Rocks From The NE Rhenish Massif, Germany

NASA Astrophysics Data System (ADS)

Zwing, A.; Matzka, J.; Bachtadse, V.; Soffel, H. C.

Previous studies on remagnetised carbonate rocks from the North American and Eu- ropean Variscides reported characteristic rock magnetic properties which are thought to be diagnostic for a chemical remagnetisation event. Their hysteresis properties with high ratios of Mrs/Ms and Hcr/Hc indicate the presence of a mixture of single-domain and superparamagnetic magnetite (Jackson, et al. 1990). In order to test if this fin- gerprint can be identified in remagnetised carbonate and clastic rocks from the NE Rhenish Massif, Germany, a series of rock magnetic experiments has been carried out. The hysteresis properties of the remagnetised clastic rocks indicate the domi- nance of large MD particles, as can be expected for detrital sediments. The carbon- ates yield significantly higher ratios of Mrs/Ms and Hcr/Hc than the clastic rocks, but only partly correspond to the characteristic properties of remagnetised carbon- ates described above. The latter might be attributed to detrital input into the carbonate platforms. Additional low-temperature remanence measurements show a wide vari- ety of phenomena, including Verwey transitions and indications for the presence of superparamagnetic grains. However, the low-temperature experiments do not allow a straightforward discrimination between the clastic and carbonate rocks and suggest more complex magnetomineralogies than expected from the hysteresis measurements alone.
Numerical modelling of fluid-rock interactions: Lessons learnt from carbonate rocks diagenesis studies

NASA Astrophysics Data System (ADS)

Nader, Fadi; Bachaud, Pierre; Michel, Anthony

2015-04-01

Quantitative assessment of fluid-rock interactions and their impact on carbonate host-rocks has recently become a very attractive research topic within academic and industrial realms. Today, a common operational workflow that aims at predicting the relevant diagenetic processes on the host rocks (i.e. fluid-rock interactions) consists of three main stages: i) constructing a conceptual diagenesis model including inferred preferential fluids pathways; ii) quantifying the resulted diagenetic phases (e.g. depositing cements, dissolved and recrystallized minerals); and iii) numerical modelling of diagenetic processes. Most of the concepts of diagenetic processes operate at the larger, basin-scale, however, the description of the diagenetic phases (products of such processes) and their association with the overall petrophysical evolution of sedimentary rocks remain at reservoir (and even outcrop/ well core) scale. Conceptual models of diagenetic processes are thereafter constructed based on studying surface-exposed rocks and well cores (e.g. petrography, geochemistry, fluid inclusions). We are able to quantify the diagenetic products with various evolving techniques and on varying scales (e.g. point-counting, 2D and 3D image analysis, XRD, micro-CT and pore network models). Geochemical modelling makes use of thermodynamic and kinetic rules as well as data-bases to simulate chemical reactions and fluid-rock interactions. This can be through a 0D model, whereby a certain process is tested (e.g. the likelihood of a certain chemical reaction to operate under specific conditions). Results relate to the fluids and mineral phases involved in the chemical reactions. They could be used as arguments to support or refute proposed outcomes of fluid-rock interactions. Coupling geochemical modelling with transport (reactive transport model; 1D, 2D and 3D) is another possibility, attractive as it provides forward simulations of diagenetic processes and resulting phases. This contribution is based on several studies that were undertaken on carbonate rocks diagenesis in some of the major reservoir rocks in the Middle East and outcrop analogues in Europe. Here, the main processes at hand are related to fracture-related dolomitization and carbonate dissolution. We would like to present the workflows we have followed and the questioning that resulted for a series of case studies. The way forward, seems evident as the integration of workflows and numerical modelling tools at different scales, bringing better constrains on the boundary data and less uncertainty.
Unravelling the structural control of mississippi valley-type deposits and prospects in carbonate sequences of the Western Canada Sedimentary Basin

USGS Publications Warehouse

Pana, D.

2006-01-01

Re-examination of selected MVT outcrops and cores in the Interior Plains and Rocky Moun-tains of Alberta, corroborated with previous paragenetic, isotopic and structural data, suggests Laramide structural channelling of dolomitizing and mineralizing fluids into strained carbonate rocks. At Pine Point, extensional faults underlying the trends of MVT ore bodies and brittle faults overprinting the Great Slave Lake Shear Zone define apinnate fault geometry and appear to be kinematically linked. Chemical and isotopic characteristics of MVT parental fluids are consistent with seawater and brine convection within fault-confined verticalaquifers, strong water-basement rock interaction, metalleaching from the basement, and focused release of hydrothermal fluids within linear zones of strained carbonate caprocks. Zones of recurrent strain in the basement and a cap of carbonate strata constitute the critical criteria for MVTexploration target selection in the WCSB.
Microstructural record of pressure solution and crystal plastic deformation in carbonate fault rocks from a shallow crustal strike-slip fault, Northern Calcareous Alps (Austria)

NASA Astrophysics Data System (ADS)

Bauer, Helene; Rogowitz, Anna; Grasemann, Benhard; Decker, Kurt

2017-04-01

This study presents microstructural investigations of natural carbonate fault rocks that formed by a suite of different deformation processes, involving hydro-fracturing, dissolution-precipitation creep and cataclasis. Some fault rocks show also clear indications of crystal plastic deformation, which is quite unexpected, as the fault rocks were formed in an upper crustal setting, raising the question of possible strongly localised, low temperature ductile deformation in carbonate rocks. The investigated carbonate fault rocks are from an exhumed, sinistral strike-slip fault at the eastern segment of the Salzachtal-Ennstal-Mariazell-Puchberg (SEMP) fault system in the Northern Calcareous Alps (Austria). The SEMP fault system formed during eastward lateral extrusion of the Eastern Alps in the Oligocene to Lower Miocene. Based on vitrinite reflectance data form intramontane Teritary basins within the Northern Calcareous Alps, a maximum burial depth of 4 km for the investigated fault segment is estimated. The investigated fault accommodated sinistral slip of several hundreds of meters. Microstructural analysis of fault rocks includes scanning electron microscopy, optical microscopy and electron backscattered diffraction mapping. The data show that fault rocks underwent various stages of evolution including early intense veining (hydro-fracturing) and stylolite formation reworked by localised shear zones. Cross cutting relationship reveals that veins never cross cut clay seams accumulated along stylolites. We conclude that pressure solution processes occured after hydro-fracturing. Clay enriched zones localized further deformation, producing a network of small-scale clay-rich shear zones of up to 1 mm thickness anastomosing around carbonate microlithons, varying from several mm down to some µm in size. Clay seams consist of kaolinit, chlorite and illite matrix and form (sub) parallel zones in which calcite was dissolved. Beside pressure solution, calcite microlithons show also ductile deformation microstructures, including deformation twinning, undulose extinction, subgrain rotation recrystallization and even grain boundary migration. Especially coarse grained calcites from veins localized ductile deformation and record dislocation glide. The investigated fault rocks are excellent examples of frictional, pressure solution and crystal plastic deformation processes. We speculated that crystal plastic deformation typical for higher metamorphic shear zones in marbles, can be either produced under much lower temperature conditions or the temperature necessary for crystal plastic deformation was generated by frictional slip or strain heating within the fault zone.
High-porosity Cenozoic carbonate rocks of South Florida: Progressive loss of porosity with depth

USGS Publications Warehouse

Halley, Robert B.; Schmoker, James W.

1983-01-01

Porosity measurements by borehole gravity meter in subsurface Cenozoic carbonates of south Florida reveal an extremely porous mass of limestone and dolomite which is transitional in total pore volume between typical porosity values for modern carbonate sediments and ancient carbonate rocks. A persistent decrease of porosity with depth, similar to that of chalks of the Gulf Coast, occurs in these rocks. We make no attempt to differentiate depositional or diagenetic facies which produce scatter in the porosity-depth relationship; the dominant data trends thus are functions of carbonate rocks in general rather than of particular carbonate facies. Carbonate strata with less than 20% porosity are absent from the rocks studied here.Aquifers and aquicludes cannot be distinguished on the basis of porosity. Although aquifers are characterized by great permeability and well-developed vuggy and even cavernous porosity in some intervals, they are not exceptionally porous when compared to other Tertiary carbonate rocks in south Florida. Permeability in these strata is governed more by the spacial distribution of pore space and matrix than by the total volume of porosity present.Dolomite is as porous as, or slightly less porous than, limestones in these rocks. This observation places limits on any model proposed for dolomitization and suggests that dolomitization does not take place by a simple ion-for-ion replacement of magnesium for calcium. Dolomitization may be selective for less porous limestone, or it may involve the incorporation of significant amounts of carbonate as well as magnesium into the rock.The great volume of pore space in these rocks serves to highlight the inefficiency of early diagenesis in reducing carbonate porosity and to emphasize the importance of later porosity reduction which occurs during the burial or late near-surface history of limestones and dolomites.
A relationship between porosity and permeability of carbonate rock reservoirs

NASA Astrophysics Data System (ADS)

Lee, J.; Park, Y.; Jo, Y.; Jeong, J.; Eom, S.

2009-12-01

Most of oil reservoirs in the world occur in carbonate rocks. Thus, characterization of the carbonate reservoirs, including understanding the correlation between porosity and permeability is essentially required to enhance oil recovery. Compared with the other sedimentary rocks such as sandstone and shale, the carbonate rocks would exhibit a wide variety of vertical and horizontal heterogeneities. In general, pores of the carbonate rocks can be affected by mineral dissolution, replacement by other minerals and re-crystallization, which are the post-depositional processes. Permeability has been estimated at a wide scale by thin section image analysis, rock core experiments, geophysical well logging data and large scale aquifer tests. For the same porosity, the permeability might show a wide variation. In this study, a large number of the porosity and the permeability data pairs for world wide carbonate rocks (reservoirs) were collected from many literatures. The porosity and permeability data were grouped according to test scale, the reservoir location and the rock types. As is already known, the relation showed a rather scattered distribution also in this study, not monotonous, which indicates that higher porosity does not mean higher permeability of the rock formation. This study provides the analysis results and implications for oil production of the carbonate reservoirs. This research was funded by Energy Efficiency and Resources Program of KETEP (Korea Institute of Energy Technology Evaluation and Planning), Grant No. 2009T100200058.
Natural Serpentinite Carbonation at Linnajavri, N-Norway (Invited)

NASA Astrophysics Data System (ADS)

Beinlich, A.; Tominaga, M.; Pluemper, O.; Hoevelmann, J.; Tivey, M.; Andrade Lima, E.; Weiss, B. P.; Austrheim, H.; Jamtveit, B.

2013-12-01

Investigation of natural mafic and ultramafic rock carbonation driven by the infiltration of CO2-bearing fluids into a solid rock unit provides insight into feedback mechanisms that may become important for in situ sequestration schemes of anthropogenic CO2. We present observations from massively carbonated serpentinites at Linnajavri, N-Norway, where completely serpentinized fragments of the dismembered ophiolite are hydrothermally altered on a km-scale to ophicarbonate (serpentine + Mg-carbonate), soapstone (talc + Mg-carbonate) and listvenite (quartz + Mg-carbonate). Field observations indicate that tectonic preprocessing of the serpentinite facilitated fluid infiltration. Listvenite is indicative of the most intense carbonation and is present along the tectonic contact of the ophiolite with the underlying carbonate-mica schist. Soapstone/steatite is indicative of less intense carbonation, forms m-wide reaction halos around fractures within the serpentinite and is also present as massive body between the listvenite and unaltered serpentinite. Sharp reaction interfaces between the soapstone and serpentinite can be traced for several hundred meters and are defined by the breakdown of antigorite to form magnesite and talc. The soapstone-listvenite transition zones are not entirely exposed in the field and are less than 5 m wide. 18O thermometry using the isotopic composition of quartz/talc and coexisting magnesite derived from veins and bulk rock samples indicate an isothermal formation of listvenite and soapstone at ~275°C. The corresponding isotopic signature of the fluid (δ13CVPDB = 2.2(5) ‰) derived from the δ13C composition of magnesite suggests an interaction with crustal rocks and devolatilization of associated overthrusted sediments as a possible source for the CO2. He- and Hg-porosimetry data, mass-balance calculations, and the preservation of serpentinite structures imply an isovolumetric alteration, which indicates that the carbonation declined due to the cessation of externally supplied CO2. The presence of sharp alteration fronts implies that reaction rates were fast relative to CO2 transport rates. Carbonation at Linnajavri was accompanied by partial dissolution of (Cr)-magnetite and incorporation of the released Fe in precipitating carbonate minerals. SQUID microscopy mapping of both natural remanence magnetization (NRM) and anhysteretic remanence magnetization (ARM) confirms different bulk intensities for the serpentinite, soapstone and listvenite samples. The alteration dependent distribution of ferromagnetic minerals suggests that magnetic surface mapping may represent a powerful tool to localize the position of reaction fronts between pristine and carbonated rock types and hence the spatial extent of the carbonation progress.

The Effect of Micrite on Velocity, Its Sensitivity to Pressure, and Dissolution of Carbonates

NASA Astrophysics Data System (ADS)

El Husseiny, A.; Vanorio, T.

2014-12-01

This study investigates the effect of micrite on the acoustic properties of well-controlled microstructures created in the laboratory to closely mimic carbonate rocks. In particular, we examine the effect of micrite content on the elastic stiffness rock, its sensitivity to pressure, and induced dissolution upon saturation with a reactive fluid. We followed Dunham's classification and fabricated the samples by mixing coarse (sand size) and very fine (micrite size) calcite grains in different ratios, with the addition of cement and then cold-compressing the mixture. The acoustic velocities were measured under bench-top conditions and as functions of confining pressure before and after the injection of a CO2aqueous solution. Our bench-top measurements indicated that micrite makes the frame of the carbonate samples stiffer. Since the sensitivity of the elastic stiffness to pressure decreases as the content of micrite increases (see figure 1), we hypothesize a stiffer pore structure (i.e., rounder pores) in micrite-richer fabrics. Furthermore, the presence of micrite makes the carbonate sample more reactive upon dissolution. The concentration of Ca+2 cations in the fluid measured at the outlet after the injection of the CO2 aqueous solution shows larger dissolution in the micrite-rich samples likely due to the higher surface area of the micrite aggregates. The content of micrite also seems to affect the evolution of stiffness as dissolution proceeds. As the content of micrite increases, the enhanced dissolution translates into a marked softening of the rock frame. We conclude that the content of micrite can play an important role in the complex rock-fluid interaction of carbonates as well as when comparing Gassmann's predictions to velocity measurements of saturated carbonates.
Morphological evaluation of heterogeneous oolitic limestone under pressure and fluid flow using X-ray microtomography

NASA Astrophysics Data System (ADS)

Zhang, Yihuai; Lebedev, Maxim; Al-Yaseri, Ahmed; Yu, Hongyan; Nwidee, Lezorgia N.; Sarmadivaleh, Mohammad; Barifcani, Ahmed; Iglauer, Stefan

2018-03-01

Pore-scale analysis of carbonate rock is of great relevance to the oil and gas industry owing to their vast application potentials. Although, efficient fluid flow at pore scale is often disrupted owing to the tight rock matrix and complex heterogeneity of limestone microstructures, factors such as porosity, permeability and effective stress greatly impact the rock microstructures; as such an understanding of the effect of these variables is vital for various natural and engineered processes. In this study, the Savonnières limestone as a carbonate mineral was evaluated at micro scales using X-ray micro-computed tomography at high resolutions (3.43 μm and 1.25 μm voxel size) under different effective stress (0 MPa, 20 MPa) to ascertain limestone microstructure and gas permeability and porosity effect. The waterflooding (5 wt% NaCl) test was conducted using microCT in-situ scanning and nanoindentation test was also performed to evaluate microscale geomechanical heterogeneity of the rock. The nanoindentation test results showed that the nano/micro scale geomechanical properties are quite heterogeneous where the indentation modulus for the weak consolidated area was as low as 1 GPa. We observed that the fluid flow easily broke some less-consolidated areas (low indentation modulus) area, coupled with increase in porosity; and consistent with fines/particles migration and re-sedimentation were identified, although the effective stress showed only a minor effect on the rock microstructure.
Total petroleum systems of the Paleozoic and Jurassic, Greater Ghawar Uplift and adjoining provinces of central Saudi Arabia and northern Arabian-Persian Gulf

USGS Publications Warehouse

Pollastro, Richard M.

2003-01-01

Oil of the Arabian Sub-Basin Tuwaiq/Hanifa-Arab TPS is sourced by organic-rich, marine carbonates of the Jurassic Tuwaiq Mountain and Hanifa Formations. These source rocks were deposited in two of three intraplatform basins during the Jurassic and, where thermally mature, have generated a superfamily of oils with distinctive geochemical characteristics. Oils were generated and expelled from these source rocks beginning in the Cretaceous at about 75 Ma. Hydrocarbon production is from 3 cyclic carbonate-rock reservoirs of the Arab Formation that are sealed by overlying anhydrite. Several giant and supergiant fields, including the world's largest oil field at Ghawar, Saudi Arabia, produce mostly from the Arab carbonate-rock reservoirs. Two assessment units are also recognized in the Arabian Sub-Basin Tuwaiq/Hanifa-Arab TPS that are similarly related to structural trap style and presence of underlying Infracambrian salt: (1) an onshore Horst-Block Anticlinal Oil AU, and (2) a mostly offshore Salt-Involved Structural Oil AU. The mean total volume of undiscovered resource for the Arabian Sub-Basin Tuwaiq/Hanifa-Arab TPS is estimated at about 49 billion barrels of oil equivalent (42 billion barrels of oil, 34 trillion feet of gas, and 1.4 billion barrels of natural gas liquids).
Plant regulation of greenhouse gas emissions and carbon lability in a Neotropical peatland

NASA Astrophysics Data System (ADS)

Girkin, Nicholas; Vane, Christopher; Turner, Benjamin; Ostle, Nicholas; Sjogersten, Sofie

2017-04-01

Tropical peatlands are under significant threat from land use changes but there remains a significant knowledge gap regarding the influences of contrasting plant types on greenhouse gas emissions and belowground carbon dynamics. We investigated differences in surface CO2 and CH4 fluxes and differences in soil organic carbon chemistry under contrasting surface vegetation types, a palm (Raphia taedigera) and a broadleaved evergreen tree (Campnosperma panamensis), in a Neotropical peatland. CO2 and CH4 production differed significantly between species, with higher fluxes measured under R. taedigera. There were significant differences in peat carbon properties under each species as revealed by Rock-Eval pyrolysis. Peat from under each species showed contrasting trends in degradation inside and outside the rooting zone, and strong differences in the presence of the most labile fractions of carbon. These results highlight the strong impacts that surface vegetation can have on surface gas emissions as well as the influences exerted on peat carbon chemistry within a tropical forested peatland, with implications for our understanding of changes in land use type across the tropics.
Geology of the Devils Hole area, Nevada

USGS Publications Warehouse

Carr, W.J.

1988-01-01

Detailed and reconnaissance mapping of the Devils Hole, Nevada, area has improved definition of the local geologic structure within a regional carbonate aquifer near its primary discharge points -- the springs of Ash Meadows. Several formerly unmapped calcite veins, and other young calcite-lined paleo-spring feeder zones were found, as well as a number of previously unknown small collapse areas in the limestone. Although the predominant structural grain of the area is oriented northwest, the importance of the very subordinate northeast-striking faults and fractures is underscored by their association with Devils Hole itself, with most of the collapse depressions, and with many of the calcite veins in ' lake beds ' and alluvium. Probable channeling of groundwater flow may occur along one important northeast-striking fault zone. The persistent tendency for openings may have been facilitated by underlying low-angle faults that separate brittle carbonate rocks from underlying, less-competent clastic rocks. (Author 's abstract)
The feasibility of TEA CO2 laser-induced plasma for spectrochemical analysis of geological samples in simulated Martian conditions

NASA Astrophysics Data System (ADS)

Savovic, Jelena; Stoiljkovic, Milovan; Kuzmanovic, Miroslav; Momcilovic, Milos; Ciganovic, Jovan; Rankovic, Dragan; Zivkovic, Sanja; Trtica, Milan

2016-04-01

The present work studies the possibility of using pulsed Transversely Excited Atmospheric (TEA) carbon dioxide laser as an energy source for laser-induced breakdown spectroscopy (LIBS) analysis of rocks under simulated Martian atmospheric conditions. Irradiation of a basaltic rock sample with the laser intensity of 56 MW cm- 2, in carbon-dioxide gas at a pressure of 9 mbar, created target plasma with favorable conditions for excitation of all elements usually found in geological samples. Detection limits of minor constituents (Ba, Cr, Cu, Mn, Ni, Sr, V, and Zr) were in the 3 ppm-30 ppm range depending on the element. The precision varied between 5% and 25% for concentration levels of 1% to 10 ppm, respectively. Generally, the proposed relatively simple TEA CO2 laser-LIBS system provides good sensitivity for geological studies under reduced CO2 pressure.
Publications - GMC 13 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 13 Publication Details Title: Total organic carbon, rock-eval pyrolysis and vitrinite information. Bibliographic Reference Phillips Petroleum Company, 1983, Total organic carbon, rock-eval K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite Reflectance Top of Page
Publications - GMC 127 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 127 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite information. Bibliographic Reference Unknown, 1989, Total organic carbon, rock-eval pyrolysis, and vitrinite ) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite Reflectance Top of Page Department
The Shublik Formation and adjacent strata in northeastern Alaska description, minor elements, depositional environments and diagenesis

USGS Publications Warehouse

Tourtelot, Harry Allison; Tailleur, Irvin L.

1971-01-01

The Shublik Formation (Middle and Late Triassic) is widespread in the surface and subsurface of northern Alaska. Four stratigraphic sections along about 70 miles of the front of the northeastern Brooks Range east of the Canning giver were examined and sampled in detail in 1968. These sections and six-step spectrographic and carbon analyses of the samples combined with other data to provide a preliminary local description of the highly organic unit and of the paleoenvironments. Thicknesses measured between the overlying Kingak Shale of Jurassic age and the underlying Sadlerochit Formation of Permian and Triassic age range from 400 to more than 800 feet but the 400 feet, obtained from the most completely exposed section, may be closer to the real thickness across the region. The sections consist of organic-rich, phosphatic, and fossiliferous muddy, silty, or carbonate rocks. The general sequence consists, from the bottom up, of a lower unit of phosphatic siltstone, a middle unit of phosphatic carbonate rocks, and an upper unit of shale and carbonate rocks near the Canning River and shale, carbonate rocks, and sandstone to the east. Although previously designated a basal member of the Kingak Shale (Jurassic), the upper unit is here included with the Shublik on the basis of its regional lithologic relation. The minor element compositions of the samples of the Shublik Formation are consistent with their carbonaceous and phosphatic natures in that relatively large amounts of copper, molybdenum, nickel, vanadium and rare earths are present. The predominantly sandy rocks of the underlying Sadlerochit Formation (Permian and Triassic) have low contents of most minor elements. The compositions of samples of Kingak Shale have a wide range not readily explicable by the nature of the rock: an efflorescent sulfate salt contains 1,500 ppm nickel and 1,500 ppm zinc and large amounts of other metals derived from weathering of pyrite and leaching of local shale. The only recorded occurrence of silver and 300 ppm lead in gouge along a shear plane may be the result of metals introduced from an extraneous source. The deposits reflect a marine environment that deepened somewhat following deposition of the Sadlerochit Formation and then shoaled during deposition of the upper limestone-siltstone unit. This apparently resulted from a moderate transgression and regression of the sea with respect to a northwest-trending line between Barrow and the Brooks Range at the International Boundary. Nearer shore facies appear eastward. The phosphate in nodules, fossil molds and oolites, appears to have formed diagenetically within the uncompacted sediment.
Modeling a CO2 mineralization experiment of fractured peridotite from the Semail ophiolite/ Oman

NASA Astrophysics Data System (ADS)

Muller, Nadja; Zhang, Guoxiang; van Noort, Reinier; Spiers, Chris; Ten Grotenhuis, Saskia; Hoedeman, Gerco

2010-05-01

Most geologic CO2 sequestration technologies focus on sedimentary rocks, where the carbon dioxide is stored in a fluid phase. A possible alternative is to trap it as a mineral in the subsurface (in-situ) in basaltic or even (ultra)mafic rocks. Carbon dioxide in aqueous solution reacts with Mg-, Ca-, and Fe-bearing silicate minerals, precipitates as (MgCa,Fe)CO3 (carbonate), and can thus be permanently sequestered. The cation donors are silicate minerals such as olivine and pyroxene which are abundant in (ultra)mafic rocks, such as peridotite. Investigations are underway to evaluate the sequestration potential of the Semail Ophiolite in Oman, utilizing the large volumes of partially serpentinized peridotite that are present. Key factors are the rate of mineralization due to dissolution of the peridotite and precipitation of carbonate, the extent of the natural and hydraulic fracture network and the accessibility of the rock to reactive fluids. To quantify the influence of dissolution rates on the overall CO2 mineralization process, small, fractured peridotite samples were exposed to supercritical CO2 and water in laboratory experiments. The samples are cored from a large rock sample in the dimension of small cylinders with 1 cm in height and diameter, with a mass of ~2g. Several experimental conditions were tested with different equipment, from large volume autoclave to small volume cold seal vessel. The 650 ml autoclave contained 400-500g of water and a sample under 10 MPa of partial CO2 pressure up to 150. The small capsules in the cold seal vessel held 1-1.5g of water and the sample under CO2 partial pressure from 15MPa to 70 MPa and temperature from 60 to 200°C. The samples remained for two weeks in the reaction vessels. In addition, bench acid bath experiments in 150 ml vials were performed open to the atmosphere at 50-80°C and pH of ~3. The main observation was that the peridotite dissolved two orders of magnitude slower in the high pressure and temperature cell of the cold seal vessel than comparative experiments in large volume autoclaves and bench acid bath vials under lower and atmospheric pressure conditions. We attributed this observation to the limited water availability in the cold seal vessel, limiting the aqueous reaction of bi-carbonate formation and magnesite precipitation. To test this hypothesis, one of the cold seal vessel experiments at 20 MPa and 100°C was simulated with a reactive transport model, using TOUGHREACT. To simulate the actual experimental conditions, the model used a grid on mm and 100's of μm scale and a fractured peridotite medium with serpentine filling the fractures. The simulation produced dissolution comparable to the experiment and showed an effective shut down of the bi-carbonation reaction within one day after the start of the experiment. If the conditions of limited water supply seen in our experiments are applicable in a field setting, we could expect dissolution may be limited by the buffering of the pH and shut down of the bi-carbonate formation. Under field conditions water and CO2 will only flow in hydraulic induced fractures and the natural fracture network that is filled with serpentine and some carbonate. The simulation result and potential implication for the field application will require further experimental investigation in the lab or field in the future.
Static versus dynamic fracturing in shallow carbonate fault zones

NASA Astrophysics Data System (ADS)

Fondriest, M.; Doan, M. L.; Aben, F. M.; Fusseis, F.; Mitchell, T. M.; Di Toro, G.

2015-12-01

Moderate to large earthquakes often nucleate within and propagate through carbonates in the shallow crust, therefore several field and experimental studies were recently aimed to constrain earthquake-related deformation processes within carbonate fault rocks. In particular, the occurrence of thick belts (10-100s m) of low-strain fault-related breccias (average size of rock fragments >1 cm), which is relatively common within carbonate damage zones, was generally interpreted as resulting from the quasi-static growth of fault zones rather than from the cumulative effect of multiple earthquake ruptures. Here we report the occurrence of up to hundreds of meters thick belts of intensely fragmented dolostones along the major transpressive Foiana Fault Zone (Italian Southern Alps) which was exhumed from < 2 km depth. Such dolostones are reduced into fragments ranging from few centimeters down to few millimeters in size with ultrafine-grained layers in proximity to the principal slip zones. Preservation of the original bedding indicates a lack of significant shear strain in the fragmented dolostones which seem to have been shattered in situ. To investigate the origin of the in-situ shattered rocks, the host dolostones were deformed in uniaxial compression both under quasi-static loading (strain rate ~10-3 s-1) and dynamic loading (strain rate >50 s-1). Dolostones deformed up to failure under low-strain rate were affected by single to multiple discrete (i.e. not interconnected) extensional fractures sub-parallel to the loading direction. Dolostones deformed under high-strain rate were shattered above a strain rate threshold of ~200 s-1(strain >1.2%) while they were split in few fragments or were macroscopically intact for lower strain rates. Experimentally shattered dolostones were reduced into a non-cohesive material with most rock fragments a few millimeters in size and elongated parallel to the loading direction. Fracture networks were investigated by X-ray microtomography showing that low- and high-strain rate damage patterns are different with the latter being similar to that of natural in-situ shattered dolostones. In-situ shattered dolostones are thus interpreted as the product of off-fault dynamic stress wave loading and can potentially be used to constrain coseismic energy release in fault zones.
Publications - GMC 100 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 100 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Unknown, 1988, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance data of ditch cuttings Information gmc100.pdf (317.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite
Publications - GMC 144 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 144 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite for more information. Bibliographic Reference Unknown, 1989, Total organic carbon, rock-eval pyrolysis gmc144.pdf (104.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite Reflectance
Publications - GMC 30 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 30 Publication Details Title: Geochemical analysis (total organic carbon, rock-eval pyrolysis , Geochemical analysis (total organic carbon, rock-eval pyrolysis, vitrinite reflectance and gc/ms chromato (1.3 M) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite Reflectance Top of
Publications - GMC 101 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 101 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Unknown, 1988, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance data of ditch cuttings Information gmc101.pdf (201.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite
Publications - GMC 60 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 60 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite , Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance geochemical data for the Nechelik (125.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite Reflectance Top of
Publications - GMC 27 | Alaska Division of Geological & Geophysical Surveys

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DGGS GMC 27 Publication Details Title: Geochemical analysis (total organic carbon, rock-eval pyrolysis . Bibliographic Reference Unknown, 1995, Geochemical analysis (total organic carbon, rock-eval pyrolysis, and ; Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite Reflectance Top of Page Department of
Publications - GMC 103 | Alaska Division of Geological & Geophysical

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DGGS GMC 103 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Unknown, 1988, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance data of ditch cuttings Information gmc103.pdf (57.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite
Publications - GMC 23 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 23 Publication Details Title: Total organic carbon, rock-eval pyrolysis, visual kerogen Unknown, [n.d.], Total organic carbon, rock-eval pyrolysis, visual kerogen/vitrinite reflectance for Information gmc023.pdf (199.0 K) Keywords Kerogen; Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon
Publications - GMC 22 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 22 Publication Details Title: Total organic carbon, rock-eval pyrolysis, visual kerogen Unknown, 1984, Total organic carbon, rock-eval pyrolysis, visual kerogen/vitrinite reflectance for the gmc022.pdf (247.0 K) Keywords Kerogen; Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite

Publications - GMC 102 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 102 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Unknown, 1988, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance data of ditch cuttings Information gmc102.pdf (81.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite
Publications - GMC 124 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 124 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Reference Unknown, 1989, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance data from the Report Information gmc124.pdf (278.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon
Carbonation by fluid-rock interactions at high-pressure conditions: Implications for carbon cycling in subduction zones

NASA Astrophysics Data System (ADS)

Piccoli, Francesca; Vitale Brovarone, Alberto; Beyssac, Olivier; Martinez, Isabelle; Ague, Jay J.; Chaduteau, Carine

2016-07-01

Carbonate-bearing lithologies are the main carbon carrier into subduction zones. Their evolution during metamorphism largely controls the fate of carbon, regulating its fluxes between shallow and deep reservoirs. Recent estimates predict that almost all subducted carbon is transferred into the crust and lithospheric mantle during subduction metamorphism via decarbonation and dissolution reactions at high-pressure conditions. Here we report the occurrence of eclogite-facies marbles associated with metasomatic systems in Alpine Corsica (France). The occurrence of these marbles along major fluid-conduits as well as textural, geochemical and isotopic data indicating fluid-mineral reactions are compelling evidence for the precipitation of these carbonate-rich assemblages from carbonic fluids during metamorphism. The discovery of metasomatic marbles brings new insights into the fate of carbonic fluids formed in subducting slabs. We infer that rock carbonation can occur at high-pressure conditions by either vein-injection or chemical replacement mechanisms. This indicates that carbonic fluids produced by decarbonation reactions and carbonate dissolution may not be directly transferred to the mantle wedge, but can interact with slab and mantle-forming rocks. Rock-carbonation by fluid-rock interactions may have an important impact on the residence time of carbon and oxygen in subduction zones and lithospheric mantle reservoirs as well as carbonate isotopic signatures in subduction zones. Furthermore, carbonation may modulate the emission of CO2 at volcanic arcs over geological time scales.
Carbon dioxide released from subduction zones by fluid-mediated reactions

NASA Astrophysics Data System (ADS)

Ague, Jay J.; Nicolescu, Stefan

2014-05-01

The balance between the subduction of carbonate mineral-bearing rocks into Earth's mantle and the return of CO2 to the atmosphere by volcanic and metamorphic degassing is critical to the carbon cycle. Carbon is thought to be released from subducted rocks mostly by simple devolatilization reactions. However, these reactions will also retain large amounts of carbon within the subducting slab and have difficulty in accounting for the mass of CO2 emitted from volcanic arcs. Carbon release may therefore occur via fluid-induced dissolution of calcium carbonate. Here we use carbonate δ18O and δ13C systematics, combined with analyses of rock and fluid inclusion mineralogy and geochemistry, to investigate the alteration of the exhumed Eocene Cycladic subduction complex on the Syros and Tinos islands, Greece. We find that in marble rocks adjacent to two fluid conduits that were active during subduction, the abundance of calcium carbonate drastically decreases approaching the conduits, whereas silicate minerals increase. Up to 60-90% of the CO2 was released from the rocks--far greater than expected via simple devolatilization reactions. The δ18O of the carbonate minerals is 5-10 lighter than is typical for metamorphosed carbonate rocks, implying that isotopically light oxygen was transported by fluid infiltration from the surroundings. We suggest that fluid-mediated carbonate mineral removal, accompanied by silicate mineral precipitation, provides a mechanism for the release of enormous amounts of CO2 from subduction zones.
Thermo-mechanical Properties of Upper Jurassic (Malm) Carbonate Rock Under Drained Conditions

NASA Astrophysics Data System (ADS)

Pei, Liang; Blöcher, Guido; Milsch, Harald; Zimmermann, Günter; Sass, Ingo; Huenges, Ernst

2018-01-01

The present study aims to quantify the thermo-mechanical properties of Neuburger Bankkalk limestone, an outcrop analog of the Upper Jurassic carbonate formation (Germany), and to provide a reference for reservoir rock deformation within future enhanced geothermal systems located in the Southern German Molasse Basin. Experiments deriving the drained bulk compressibility C were performed by cycling confining pressure p c between 2 and 50 MPa at a constant pore pressure p p of 0.5 MPa after heating the samples to defined temperatures between 30 and 90 °C. Creep strain was then measured after each loading and unloading stage, and permeability k was obtained after each creep strain measurement. The drained bulk compressibility increased with increasing temperature and decreased with increasing differential pressure p d = p c - p p showing hysteresis between the loading and unloading stages above 30 °C. The apparent values of the indirectly calculated Biot coefficient α ind containing contributions from inelastic deformation displayed the same temperature and pressure dependencies. The permeability k increased immediately after heating and the creep rates were also temperature dependent. It is inferred that the alteration of the void space caused by temperature changes leads to the variation of rock properties measured under isothermal conditions while the load cycles applied under isothermal conditions yield additional changes in pore space microstructure. The experimental results were applied to a geothermal fluid production scenario to constrain drawdown and time-dependent effects on the reservoir, overall, to provide a reference for the hydromechanical behavior of geothermal systems in carbonate, and more specifically, in Upper Jurassic lithologies.
Orbital identification of carbonate-bearing rocks on Mars

USGS Publications Warehouse

Ehlmann, B.L.; Mustard, J.F.; Murchie, S.L.; Poulet, F.; Bishop, J.L.; Brown, A.J.; Calvin, W.M.; Clark, R.N.; Des Marais, D.J.; Milliken, R.E.; Roach, L.H.; Roush, T.L.; Swayze, G.A.; Wray, J.J.

2008-01-01

Geochemical models for Mars predict carbonate formation during aqueous alteration. Carbonate-bearing rocks had not previously been detected on Mars' surface, but Mars Reconnaissance Orbiter mapping reveals a regional rock layer with near-infrared spectral characteristics that are consistent with the presence of magnesium carbonate in the Nili Fossae region. The carbonate is closely associated with both phyllosilicate-bearing and olivine-rich rock units and probably formed during the Noachian or early Hesperian era from the alteration of olivine by either hydrothermal fluids or near-surface water. The presence of carbonate as well as accompanying clays suggests that waters were neutral to alkaline at the time of its formation and that acidic weathering, proposed to be characteristic of Hesperian Mars, did not destroy these carbonates and thus did not dominate all aqueous environments.
Strontium Isotopic Composition of Paleozoic Carbonate Rocks in the Nevada Test Site Vicinity, Clark, Lincoln, and Nye Counties, Nevada and Inyo County, California.

DOE Office of Scientific and Technical Information (OSTI.GOV)

James B. Paces; Zell E. Peterman; Kiyoto Futa

2007-08-07

Ground water moving through permeable Paleozoic carbonate rocks represents the most likely pathway for migration of radioactive contaminants from nuclear weapons testing at the Nevada Test Site, Nye County, Nevada. The strontium isotopic composition (87Sr/86Sr) of ground water offers a useful means of testing hydrochemical models of regional flow involving advection and reaction. However, reaction models require knowledge of 87Sr/86Sr data for carbonate rock in the Nevada Test Site vicinity, which is scarce. To fill this data gap, samples of core or cuttings were selected from 22 boreholes at depth intervals from which water samples had been obtained previously aroundmore » the Nevada Test Site at Yucca Flat, Frenchman Flat, Rainier Mesa, and Mercury Valley. Dilute acid leachates of these samples were analyzed for a suite of major- and trace-element concentrations (MgO, CaO, SiO2, Al2O3, MnO, Rb, Sr, Th, and U) as well as for 87Sr/86Sr. Also presented are unpublished analyses of 114 Paleozoic carbonate samples from outcrops, road cuts, or underground sites in the Funeral Mountains, Bare Mountain, Striped Hills, Specter Range, Spring Mountains, and ranges east of the Nevada Test Site measured in the early 1990's. These data originally were collected to evaluate the potential for economic mineral deposition at the potential high-level radioactive waste repository site at Yucca Mountain and adjacent areas (Peterman and others, 1994). Samples were analyzed for a suite of trace elements (Rb, Sr, Zr, Ba, La, and Ce) in bulk-rock powders, and 87Sr/86Sr in partial digestions of carbonate rock using dilute acid or total digestions of silicate-rich rocks. Pre-Tertiary core samples from two boreholes in the central or western part of the Nevada Test Site also were analyzed. Data are presented in tables and summarized in graphs; however, no attempt is made to interpret results with respect to ground-water flow paths in this report. Present-day 87Sr/86Sr values are compared to values for Paleozoic seawater present at the time of deposition. Many of the samples have 87Sr/86Sr compositions that remain relatively unmodified from expected seawater values. However, rocks underlying the northern Nevada Test Site as well as rocks exposed at Bare Mountain commonly have elevated 87Sr/86Sr values derived from post-depositional addition of radiogenic Sr most likely from fluids circulating through rubidium-rich Paleozoic strata or Precambrian basement rocks.« less
Strontium Isotopic Composition of Paleozoic Carbonate Rocks in the Nevada Test Site Vicinity, Clark, Lincoln, and Nye Counties, Nevada, and Inyo County, California

USGS Publications Warehouse

Paces, James B.; Peterman, Zell E.; Futo, Kiyoto; Oliver, Thomas A.; Marshall, Brian D.

2007-01-01

Ground water moving through permeable Paleozoic carbonate rocks represents the most likely pathway for migration of radioactive contaminants from nuclear weapons testing at the Nevada Test Site, Nye County, Nevada. The strontium isotopic composition (87Sr/86Sr) of ground water offers a useful means of testing hydrochemical models of regional flow involving advection and reaction. However, reaction models require knowledge of 87Sr/86Sr data for carbonate rock in the Nevada Test Site vicinity, which is scarce. To fill this data gap, samples of core or cuttings were selected from 22 boreholes at depth intervals from which water samples had been obtained previously around the Nevada Test Site at Yucca Flat, Frenchman Flat, Rainier Mesa, and Mercury Valley. Dilute acid leachates of these samples were analyzed for a suite of major- and trace-element concentrations (MgO, CaO, SiO2, Al2O3, MnO, Rb, Sr, Th, and U) as well as for 87Sr/86Sr. Also presented are unpublished analyses of 114 Paleozoic carbonate samples from outcrops, road cuts, or underground sites in the Funeral Mountains, Bare Mountain, Striped Hills, Specter Range, Spring Mountains, and ranges east of the Nevada Test Site measured in the early 1990's. These data originally were collected to evaluate the potential for economic mineral deposition at the potential high-level radioactive waste repository site at Yucca Mountain and adjacent areas (Peterman and others, 1994). Samples were analyzed for a suite of trace elements (Rb, Sr, Zr, Ba, La, and Ce) in bulk-rock powders, and 87Sr/86Sr in partial digestions of carbonate rock using dilute acid or total digestions of silicate-rich rocks. Pre-Tertiary core samples from two boreholes in the central or western part of the Nevada Test Site also were analyzed. Data are presented in tables and summarized in graphs; however, no attempt is made to interpret results with respect to ground-water flow paths in this report. Present-day 87Sr/86Sr values are compared to values for Paleozoic seawater present at the time of deposition. Many of the samples have 87Sr/86Sr compositions that remain relatively unmodified from expected seawater values. However, rocks underlying the northern Nevada Test Site as well as rocks exposed at Bare Mountain commonly have elevated 87Sr/86Sr values derived from post-depositional addition of radiogenic Sr most likely from fluids circulating through rubidium-rich Paleozoic strata or Precambrian basement rocks.
A calcium isotope test of end-Permian ocean acidification using biogenic apatite

NASA Astrophysics Data System (ADS)

Hinojosa, J.; Brown, S. T.; DePaolo, D. J.; Paytan, A.; Shen, S.; Chen, J.; Payne, J.

2011-12-01

Submarine erosional truncation of uppermost Permian carbonate strata has been interpreted to reflect ocean acidification coincident with the end-Permian mass extinction. Although this scenario is consistent with carbon isotope and paleontological data, several alternative scenarios, such as ocean overturn or collapse of the biological pump, can also account for the carbon isotope and paleontological evidence. Calcium isotopes provide a geochemical proxy to test between acidification and alternative scenarios. Specifically, a negative shift in the calcium isotope composition (δ44/40Ca) of seawater is predicted under the acidification scenario but not the alternatives. The δ44/40Ca of carbonate rocks from south China exhibits a negative excursion of approximately 0.3%, but this shift could result from either a change in the δ44/40Ca of seawater or a change in carbonate mineralogy because calcite and aragonite exhibit substantially different fractionation factors relative to seawater. To test whether the negative shift in δ44/40Ca reflects seawater δ44/40Ca or carbonate mineralogy, we measured the δ44/40Ca of conodont microfossils (calcium hydroxyapatite) from the global stratotype section for the Permian-Triassic boundary at Meishan, China. The conodont δ44/40Ca record shows a negative excursion similar in stratigraphic position and magnitude to that previously observed in carbonate rocks. Parallel negative excursions in the δ44/40Ca of carbonate rocks and conodont microfossils cannot be accounted for by a change in carbonate mineralogy but are consistent with a negative shift in the δ44/40Ca of seawater. These data add further support for the ocean acidification scenario, pointing toward strong similarities between the greatest catastrophe in the history of animal life and anticipated global change during the 21st century.
Quantifying porosity and permeability of fractured carbonates and fault rocks in natural groundwater reservoirs

NASA Astrophysics Data System (ADS)

Pirmoradi, Reza; Wolfmayr, Mariella; Bauer, Helene; Decker, Kurt

2017-04-01

This study presents porosity and permeability data for a suite of different carbonate rocks from two major groundwater reservoirs in eastern Austria that supply more than 60% of Vienna`s drinking water. Data includes a set of lithologically different, unfractured host rocks, fractured rocks with variable fracture intensities, and fault rocks such as dilation breccias, different cataclasites and dissolution-precipitation fault rocks. Fault rock properties are of particular importance, since fault zones play an important role in the hydrogeology of the reservoirs. The reservoir rocks are exposed at two major alpine karst plateaus in the Northern Calcareous Alps. They comprise of various Triassic calcareous strata of more than 2 km total thickness that reflect facies differentiation since Anisian times. Rocks are multiply deformed resulting in a partly dense network of fractures and faults. Faults differ in scale, fault rock content, and fault rock volumes. Methods used to quantify the porosity and permeability of samples include a standard industry procedure that uses the weight of water saturated samples under hydrostatic uplift and in air to determine the total effective (matrix and fracture) porosity of rocks, measurements on plugs with a fully automated gas porosity- and permeameter using N2 gas infiltrating plugs under a defined confining pressure (Coreval Poro 700 by Vinci technologies), and percolation tests. The latter were conducted in the field along well known fault zones in order to test the differences in fractured rock permeability in situ and on a representative volume, which is not ensured with plug measurements. To calculate hydraulic conductivity by the Darcy equation the measured elapsed time for infiltrating a standard volume of water into a small borehole has been used. In general, undisturbed host rock samples are all of low porosity (average around 1%). The open porosity of the undisturbed rocks belonging to diverse formations vary from 0.18% to 2.35%. Klinkenberg permeabilities of plugs range from 0.001mD to about 0.6mD thus spreading over three orders of magnitude. Fractured rocks show significantly higher porosities (3% average) with respect to the undeformed country rocks. Plug measurements reveal quite low permeabilities (< 1mD) for this type of rock, which is owed to the measuring technique, where fractures are closed under confining pressure. A second important point is that intensely fractured rocks are underrepresented in the data as they cannot be plugged adequately. Percolation tests give better information for fractured rock permeabilities and revealed hydraulic conductivities of 10-6 m/sec for little fractured to 5x10-5 m/sec for intensely fractured rocks. Plug and rock sample data show that cataclastic fault rocks can have quite high porosities (up to 4.1%). However, plug permeabilities down to 0.03mD demonstrate that pores are too small to result in any significant permeability. Breccias show high porosities of 4% in average and very variable permeabilities between 2.2mD and 2214mD depending mainly on the degree of cementation.
Reactive Transport Modeling of CO2-induced Porosity and Permeability Changes in Heterogeneous Carbonate Rocks

NASA Astrophysics Data System (ADS)

Hao, Y.; Smith, M. M.; Mason, H. E.; Carroll, S.

2015-12-01

It has long been appreciated that chemical interactions have a major effect on rock porosity and permeability evolution and may alter the behavior or performance of both natural and engineered reservoir systems. Such reaction-induced permeability evolution is of particular importance for geological CO2 sequestration and storage associated with enhanced oil recovery. In this study we used a three-dimensional Darcy scale reactive transport model to simulate CO2 core flood experiments in which the CO2-equilibrated brine was injected into dolostone cores collected from the Arbuckle carbonate reservoir, Wellington, Kansas. Heterogeneous distributions of macro pores, fractures, and mineral phases inside the cores were obtained from X-ray computed microtomography (XCMT) characterization data, and then used to construct initial model macroscopic properties including porosity, permeability, and mineral compositions. The reactive transport simulations were performed by using the Nonisothermal Unsaturated Flow and Transport (NUFT) code, and their results were compared with experimental data. It was observed both experimentally and numerically that the dissolution fronts became unstable in highly heterogeneous and less permeable formations, leading to the development of highly porous flow paths or wormholes. Our model results indicate that the continuum-scale reactive transport models are able to adequately capture the evolution of distinct dissolution fronts as observed in carbonate rocks at a core scale. The impacts of rock heterogeneity, chemical kinetics and porosity-permeability relationships were also examined in this study. The numerical model developed in this study will not only help improve understanding of coupled physical and chemical processes controlling carbonate dissolution, but also provide a useful basis for upscaling transport and reaction properties from core scale to field scale. This work was performed under the auspices of the U.S. Department of Energy by Lawrence Livermore National Laboratory under Contract DE-AC52-07NA27344.
Comparison of deformation mechanics for two different carbonates: oolitic limestone and laminites

NASA Astrophysics Data System (ADS)

Zihms, Stephanie; Lewis, Helen; Couples, Gary; Hall, Stephen; Somerville, Jim

2016-04-01

Carbonate rocks form under a range of conditions which leads to a diverse rock group. Even though carbonates are overall mineralogically simple, the solid-space distribution ranges from simple compositions such as oolitic limestones to highly complex networks of pores and solids as seen in coquinas. Their fundamental mechanical behaviour has been identified to be like clastic rocks (Vajdova 2004, Brantut, Heap et al. 2014). However it is very likely that this observation is not true for more complex carbonates. Triaxial tests were performed on cylindrical samples of two different carbonates; a) oolitic limestone (Bicqueley quarry, France) and b) laminite (Ariripe basin, Brazil). The samples were deformed under confining pressures of 8, 12 and 20MPa, and 20, 30 and 40MPa, respectively. All tests were stopped as soon as peak load was observed to preserve as many deformation characteristics as possible. Photographs of the samples were taken before and after deformation to allow surface analysis of deformation features. Additionally, samples were analysed post-deformation with X-ray tomography (XRT) (using the Zeiss XRadia XRM 520 at the 4D Imaging Lab at Lund University). The 3D tomography images represent the post-deformation samples' density distribution, allowing detailed, non-destructive, 3D analysis of the deformation features that developed in the triaxial testing, including the complex geometries and interactions of fractures, deformation bands and sedimentary layering. They also provide an insight into the complexity of deformation features produced due to the carbonate response. Initial results show that the oolitic limestone forms single shear bands almost the length of the sample, exhibiting similar characteristics to sandstones deformed under similar conditions. These features are observed for all three applied loads. The laminate sample deformed at the lowest confining pressure exhibits compactive features. However, the laminite samples deformed at the two higher confining pressures both show highly complex fracture networks comprising open fractures and fracture propagation. This suggests that the laminate changes from compactive to dilational responses over the selected confining conditions. The XRT analysis indicates that a more complex fracture distribution could be linked to rock component properties e.g. grain size and composition. For the laminite these are variable with the layers. This is in agreement with field observations of laminite microfabrics (Calvo, Rodriguez-Pascua et al. 1998). Additionally, the typical grain size of the laminate (μm) is much smaller than the oolitic limestone (mm), which suggests that fracture network complexity can also be linked to bulk system complexity i.e. pore & grain network. These deformation experiments show that, as previously observed, oolitic limestones seem to behave similarly to sandstones. However this observation is not true for laminites and it is very likely that more complex carbonates will develop even more complicated deformation behaviour. It is therefore necessary to systematically test different carbonate rocks to understand the impact of geometry and composition, as well as the interplay with the pore network. Brantut, N., et al. (2014). Journal of Geophysical Research: Solid Earth 119(7): 5444-5463. Calvo, J. P., et al. (1998). Sedimentology 45: 279-292. Vajdova, V. (2004). Journal of Geophysical Research 109(B5).
Publications - GMC 242 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 242 Publication Details Title: Total organic carbon and rock-eval pyrolysis evaluation of 21 Core Laboratories, 1995, Total organic carbon and rock-eval pyrolysis evaluation of 21 hand-picked coal Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon Top of Page Department of Natural Resources, Division
Publications - GMC 136 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 136 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and some vitrinite Unknown, 1989, Total organic carbon, rock-eval pyrolysis, and some vitrinite reflectance data of cuttings Report Information gmc136.pdf (39.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon
Publications - GMC 12 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

- 11,850 feet; total organic carbon, rock-eval pyrolysis and visual kerogen/vitrinite reflectance Authors River #1 well 10,255 - 11,850 feet; total organic carbon, rock-eval pyrolysis and visual kerogen gmc012.pdf (384.0 K) Keywords Kerogen; Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite
Publications - GMC 24 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 24 Publication Details Title: Total organic carbon, rock-eval pyrolysis, visual kerogen Unknown, [n.d.], Total organic carbon, rock-eval pyrolysis, visual kerogen/vitrinite reflectance of the Information gmc024.pdf (79.0 K) Keywords Kerogen; Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon
DOE Office of Scientific and Technical Information (OSTI.GOV)

Lu, D.Y.; Hughes, R.W.; Anthony, E.J.

Sintering during calcination/carbonation may introduce substantial economic penalties for a CO{sub 2} looping cycle using limestone/dolomite-derived sorbents. Cyclic carbonation and calcination reactions were investigated for CO{sub 2} capture under fluidized bed combustion (FBC) conditions. The cyclic carbonation characteristics of CaCO{sub 3}-derived sorbents were compared at various calcination temperatures (700-925{sup o} C) and different gas stream compositions: pure -2 and a realistic calciner environment where high concentrations of CO{sub 2}>80-90% are expected. The conditions during carbonation were 700 {sup o}C and 15% CO{sub 2} in N{sub 2} and 0.18% or 0.50% SO{sub 2} in selected tests. Up to 20 calcination/carbonation cyclesmore » were conducted using a thermogravimetric analyzer (TGA) apparatus. Three Canadian limestones were tested: Kelly Rock, Havelock, and Cadomin, using a prescreened particle size range of 400-650 {mu} m. Calcined Kelly Rock and Cadomin samples were hydrated by steam and examined. Sorbent reactivity was reduced whenever SO{sub 2} was introduced to either the calcining or carbonation streams. The multicyclic capture capacity of CaO for CO{sub 2} was substantially reduced at high concentrations of CO{sub 2} during the sorbent regeneration process and carbonation conversion of the Kelly Rock sample obtained after 20 cycles was only 10.5%. Hydrated sorbents performed better for CO{sub 2} capture but showed deterioration following calcination in high CO{sub 2} gas streams indicating that high CO{sub 2} and SO{sub 2} levels in the gas stream lead to lower CaO conversion because of enhanced sintering and irreversible formation of CaSO{sub 4}.« less
Factors affecting groundwater quality in the Valley and Ridge aquifers, eastern United States, 1993-2002

USGS Publications Warehouse

Johnson, Gregory C.; Zimmerman, Tammy M.; Lindsey, Bruce D.; Gross, Eliza L.

2011-01-01

Chemical and microbiological analyses of water from 230 wells and 35 springs in the Valley and Ridge Physiographic Province, sampled between 1993 and 2002, indicated that bedrock type (carbonate or siliciclastic rock) and land use were dominant factors influencing groundwater quality across a region extending from northwestern Georgia to New Jersey. The analyses included naturally occurring compounds (major mineral ions and radon) and anthropogenic contaminants [pesticides and volatile organic compounds (VOCs)], and contaminants, such as nitrate and bacteria, which commonly increase as a result of human activities. Natural factors, such as topographic position and the mineral composition of underlying geology, act to produce basic physical and geochemical conditions in groundwater that are reflected in physical properties, such as pH, temperature, specific conductance, and alkalinity, and in chemical concentrations of dissolved oxygen, radon, and major mineral ions. Anthropogenic contaminants were most commonly found in water from wells and springs in carbonate-rock aquifers. Nitrate concentrations exceeded U.S. Environmental Protection Agency maximum contaminant levels in 12 percent of samples, most of which were from carbonate-rock aquifers. Escherichia coli (E. coli), pesticide, and VOC detection frequencies were significantly higher in samples from sites in carbonate-rock aquifers. Naturally occurring elements, such as radon, iron, and manganese, were found in higher concentrations in siliciclastic-rock aquifers. Radon levels exceeded the proposed maximum contaminant level of 300 picocuries per liter in 74 percent of the samples, which were evenly distributed between carbonate- and siliciclastic-rock aquifers. The land use in areas surrounding wells and springs was another significant explanatory variable for the occurrence of anthropogenic compounds. Nitrate and pesticide concentrations were highest in samples collected from sites in agricultural areas and lowest in samples collected from sites in undeveloped areas. Volatile organic compounds were detected most frequently and in highest concentrations in samples from sites in urban areas, and least frequently in agricultural and undeveloped areas. No volatile organic compound concentrations and concentrations from only one pesticide, dieldrin, exceeded human-health benchmarks.
Distribution of organic carbon and petroleum source rock potential of Cretaceous and lower Tertiary carbonates, South Florida Basin: preliminary results

USGS Publications Warehouse

Palacas, James George

1978-01-01

Analyses of 134 core samples from the South Florida Basin show that the carbonates of Comanchean age are relatively richer in average organic carbon (0.41 percent) than those of Coahuilan age (0.28 percent), Gulfian age (0.18 percent) and Paleocene age (0.20 percent). They are also nearly twice as rich as the average world, wide carbonate (average 0.24 percent). The majority of carbonates have organic carbons less than 0.30 percent but the presence of many relatively organic rich beds composed of highly bituminous, argillaceous, highly stylolitic, and algal-bearing limestones and dolomites accounts for the higher percentage of organic carbon in some of the stratigraphic units. Carbonate rocks that contain greater than 0.4 percent organic carbon and that might be considered as possible petroleum sources were noted in almost each subdivision of the Coahuilan and Comanchean Series but particularly the units of Fredericksburg 'B', Trinity 'A', Trinity 'F', and Upper Sunniland. Possible source rocks have been ascribed by others to the Lower Sunniland, but lack of sufficient samples precluded any firm assessment in this initial report. In the shallower section of the basin, organic-rich carbonates containing as much as 3.2 percent organic carbon were observed in the lowermost part of the Gulfian Series and carbonate rocks with oil staining or 'dead' and 'live oil' were noted by others in the uppermost Gulfian and upper Cedar Keys Formation. It is questionable whether these shallower rocks are of sufficient thermal maturity to have generated commercial oil. The South Florida basin is still sparsely drilled and produces only from the Sunniland Limestone at an average depth of 11,500 feet (3500 m). Because the Sunniland contains good reservoir rocks and apparently adequate source rocks, and because the success rate of new oil field discoveries has increased in recent years, the chances of finding additional oil reserves in the Sunniland are promising. Furthermore, the presence of possible source rocks in many of the other stratigraphic units, in particular, the Fredericksburg, should give further impetus to exploring for other productive horizons.
Sulfur, carbon, and oxygen isotope variations in submarine hydrothermal deposits of Guaymas Basin, Gulf of California, USA

USGS Publications Warehouse

Peter, J.M.; Shanks, Wayne C.

1992-01-01

Sulfur, carbon, and oxygen isotope values were measured in sulfide, sulfate, and carbonate from hydrothermal chimney, spire, and mound samples in the southern trough of Guaymas Basin, Gulf of California, USA. ??34S values of sulfides range from -3.7 to 4.5%. and indicate that sulfur originated from several sources: 1. (1) dissolution of 0??? sulfide contained within basaltic rocks, 2. (2) thermal reduction of seawater sulfate during sediment alteration reactions in feeder zones to give sulfide with positive ??34S, and 3. (3) entrainment or leaching of isotopically light (negative-??34S) bacteriogenic sulfide from sediments underlying the deposits. ??34S of barite and anhydrite indicate sulfur derivation mainly from unfractionated seawater sulfate, although some samples show evidence of sulfate reduction and sulfide oxidation reactions during mixing within chimneys. Oxygen isotope temperatures calculated for chimney calcites are in reasonable agreement with measured vent fluid temperatures and fluid inclusion trapping temperatures. Hydrothermal fluids that formed calcite-rich chimneys in the southern trough of Guaymas Basin were enriched in 18O with respect to seawater by about 2.4??? due to isotopic exchange with sedimentary and/or basaltic rocks. Carbon isotope values of calcite range from -9.6 to -14.0??? ??34CpDB, indicating that carbon was derived in approximately equal quantities from the dissolution of marine carbonate minerals and the oxidation of organic matter during migration of hydrothermal fluid through the underlying sediment column. Statistically significant positive, linear correlations of ??34S, ??34C, and ??18O of sulfides and calcites with geographic location within the southern trough of Guaymas Basin are best explained by variations in water/rock ( w r) ratios or sediment reactivity within subsurface alteration zones. Low w r ratios and the leaching of detrital carbonates and bacteriogenic sulfides at the southern vent sites result in relatively high ??13C and low ??34S in chimney carbonates and sulfides, respectively. In the north, where the depletion of alkalis in vent fluids indicates higher w r ratios, positive ??34S and more negative ??13c are due to increased contributions from organic matter oxidation and sulfate reduction reactions. ?? 1992.

Development of diagenetic seals in carbonates and sandstones

DOE Office of Scientific and Technical Information (OSTI.GOV)

Schmidt, V.; Almon, W.

1983-03-01

Diagenetic seals effectively block the movement of reservoir hydrocarbons in many sandstone and carbonate rock units. Diagenetic seals in sandstones and carbonate rocks encase reservoir rocks with either depositional or diagenetic porosity. Diagenetic reservoir porosity may originate before or after the establishment of an effective diagenetic seal. Hydrocarbon traps with diagenetic seals may conform in their geometry as well to structure or stratigraphy as to diagenetic facies. Therefore, some structural and stratigraphic traps may, in part or entirely, depend on diagenetic seals. Detailed analysis of diagenetic seals in sandstones and carbonate rocks can considerably improve our ability to predict theirmore » occurrence and to recognize their spatial and temporal relationship to reservoir rocks and hydrocarbon migration.« less
Petroleum systems of the Southeast Tertiary basins and Marbella area, Southeast Mexico

DOE Office of Scientific and Technical Information (OSTI.GOV)

Fuentes, F.

1996-08-01

This study was done in an area where insufficient organic-rich rocks were available for a reliable oil-source rock correlation. However, oil-rock correlations, molecular characteristics of key horizons, paleofacies maps, maturation and potential migration pathways suggest the Tithonian as a major source rock. Moreover, there is good evidence of high quality source rocks in Oxfordian, Kimmeridgian, Middle-Upper Cretaceous and Paleogene (mainly in the Eocene). Plays were identified in Upper Jurassic oolitic sequences, Early-Middle Cretaceus carbonate platform rocks and breccias, Late Cretaceous basinal fracture carbonates, Paleogene carbonates and breccias, Early-Middle Miocene mounds and submarine fans and isolated carbonate platform sediments and Miocene-Recentmore » turbidites. Seal rocks are shaly carbonates and anhydrites from Tithonian, basinal carbonates and anhydrites from Middle-Upper Cretaceous, basinal carbonates and marls from Upper Cretaceous and Paleogene shales, and bathyal shales from Early Miocene-Recent. The first phase of oil migration from upper Jurassic-Early Cretaceous source rocks occurred in the Early-Middle Cretaceous. In the Upper Cretaceous the Chortis block collided with Chiapas, and as a result mild folding and some hydrocarbons were emplaced to the structural highs. The main phase of structuration and folding of the Sierra de Chiapas started in the Miocene, resulting in well-defined structural traps. Finally, in Plio-Pleistocene the Chortis block was separated, the major compressional period finished and the southern portion of Sierra de Chiapas was raised isostatically. As a result of major subsidence, salt withdrawal and increased burial depth, conditions were created for the generation of liquid hydrocarbons from the Paleogene shales.« less
Exploring Nested Reaction Fronts to Understand How Oxygen Cracks Rocks, Carbonic and Sulfuric Acids Dissolve Rocks, and Water Transports Rocks during Weathering

NASA Astrophysics Data System (ADS)

Brantley, S. L.; Gu, X.; Sullivan, P. L.; Kim, H.; Stinchcomb, G. E.; Lebedeva, M.; Balashov, V. N.

2016-12-01

To first order, weathering is the reaction of rocks with oxidants (oxygen, nitrate, etc.), acids (carbonic, sulfuric, and organic acids), and water. To explore weathering we have been studying the depth intervals in soils, saprolite, and weathering rock where mineral reactions are localized - "reaction fronts". We limit the study to ridges or catchments in climates where precipitation is greater than potential evapotranspiration. For example, in the Susquehanna Shale Hills Critical Zone Observatory, we observe reaction fronts that generally define very rough surfaces in 3D that mimic the land surface topography, although with lower relief. Overall, the fronts form nested curved surfaces. In Shale Hills, the deepest reaction fronts are oxidation of pyrite, and dissolution of carbonate. The carbonate is inferred to dissolve at least partly due to the sulfuric acid produced by the pyrite. In addition to pyrite, chlorite also starts to oxidize at the water table. We hypothesize that these dissolution and oxidation reactions open pores and cause microfracturing that open the rock to infiltration of advecting meteoric waters. At much shallower depths, illite is observed to dissolve. In Shale Hills, these reaction fronts - pyrite, carbonate, illite - separate over meters beneath the ridges. Such separated reaction fronts have also been observed in other fractured lithologies where oxidation is the deepest reaction and is associated with weathering-induced fractures. In contrast, in some massive mafic rocks, reaction fronts are almost co-located. By studying the geometry of reaction fronts, it may be possible to elucidate the relative importance of how oxygen cracks rocks; carbonic, organic, and sulfuric acids dissolve rocks; and water mobilizes rock materials during weathering.
In search of early life: Carbonate veins in Archean metamorphic rocks as potential hosts of biomarkers

NASA Astrophysics Data System (ADS)

Peters, Carl A.; Piazolo, Sandra; Webb, Gregory E.; Dutkiewicz, Adriana; George, Simon C.

2016-11-01

The detection of early life signatures using hydrocarbon biomarkers in Precambrian rocks struggles with contamination issues, unspecific biomarkers and the lack of suitable sedimentary rocks due to extensive thermal overprints. Importantly, host rocks must not have been exposed to temperatures above 250 °C as at these temperatures biomarkers are destroyed. Here we show that Archean sedimentary rocks from the Jeerinah Formation (2.63 billion yrs) and Carawine Dolomite (2.55 billion yrs) of the Pilbara Craton (Western Australia) drilled by the Agouron Institute in 2012, which previously were suggested to be suitable for biomarker studies, were metamorphosed to the greenschist facies. This is higher than previously reported. Both the mineral assemblages (carbonate, quartz, Fe-chlorite, muscovite, microcline, rutile, and pyrite with absence of illite) and chlorite geothermometry suggest that the rocks were exposed to temperatures higher than 300 °C and probably ∼400 °C, consistent with greenschist-facies metamorphism. This facies leads to the destruction of any biomarkers and explains why the extraction of hydrocarbon biomarkers from pristine drill cores has not been successful. However, we show that the rocks are cut by younger formation-specific carbonate veins containing primary oil-bearing fluid inclusions and solid bitumens. Type 1 veins in the Carawine Dolomite consist of dolomite, quartz and solid bitumen, whereas type 2 veins in the Jeerinah Formation consist of calcite. Within the veins fluid inclusion homogenisation temperatures and calcite twinning geothermometry indicate maximum temperatures of ∼200 °C for type 1 veins and ∼180 °C for type 2 veins. Type 1 veins have typical isotopic values for reprecipitated Archean sea-water carbonates, with δ13CVPDB ranging from - 3 ‰ to 0‰ and δ18OVPDB ranging from - 13 ‰ to - 7 ‰, while type 2 veins have isotopic values that are similar to hydrothermal carbonates, with δ13CVPDB ranging from - 18 ‰ to - 4 ‰ and δ18OVPDB ranging from - 18 ‰ to - 12 ‰. Evidently, the migration and entrapment of hydrocarbons occurred after peak metamorphism under temperatures congruous with late catagenesis and from fluids of different compositions. The relatively high temperatures of vein formation and the known geotectonic history of the rocks analysed suggest a probable minimum age of 1.8 billion yrs (Paleoproterozoic). Our results demonstrate that post peak-metamorphic veins provide an exciting opportunity in the search for evidence of early life. The integration of petrological and organic geochemical techniques is crucial for any future studies that use biomarkers to reconstruct the early biosphere.
Characterization of Possible Carbonatites in Southeast Missouri

NASA Astrophysics Data System (ADS)

Shavers, E. J.; Wulamu, A.; Encarnacion, J. P.; Luetkemeyer, P. B.

2014-12-01

Carbonatite is an igneous rock containing greater than 50% carbonate minerals. These rocks are the most common host of REE mineralization and may contain other economic deposits such as uranium, fluorine and niobium. Several researchers have mentioned the presence of a carbonatite phase interspersed among the olivine melilitite-alnöite dikes and diatremes of southeast Missouri, yet a comprehensive validation of this occurrence has, so far, remained elusive. Here we present petrographic, cathodoluminescence, stable isotope and Vis-NIR analysis which support the presence of a carbonatite magma. We identify apparently single generation calcite groundmass surrounding country rock xenoliths and olivine-cored mafic spheroids altered to carbonate and opaque minerals. We present stable isotope data for twenty samples of intrusive and country rock from across the study area. δ18O values for all rock types exhibit little variation with values between 21.9 ‰ and 28.1 ‰ (VSMOW), possibly the result of outgassing during emplacement. Measured δ13C values of (1) carbonate country rocks are between -0.1 ‰ and -2.9 ‰ (VPDB), (2) ultramafic and carbonate-rich mafic rocks range from -3.0 ‰ to -4.6 ‰ (VPDB) and (3) carbonate-rich rocks with volcanic textures, as well as carbonate veins within mafic rocks, fall between -5.4 ‰ to -8.2 ‰ (VPDB). We suggest that this data and initial petrographic observations indicate (1) limited fluid-rock interaction as the host rock clasts have retained their original isotopic signature, (2) an initial ultramafic phase enriched in 13C by a small amount of sedimentary rock due to low initial C content, (3) mantle sourced carbonate fluids entraining fragments of the ultramafic phase and xenoliths. However, future electron microprobe studies may allow us to further constrain the causes for the observed isotopic shifts. We compare laboratory reflectance measurements of a dolomitic intrusive and adjacent dolomite country rock. Absorption bands in the 0.42-1.35 and 2.2-2.4 μm regions indicate unique Si, Fe, Mg, Al and possibly Cr mineralization in the intrusive rock. These features may indicate higher chemical content in addition to, or alternately, intrusive specific mineralogy. This data may allow for future carbonatite identification using remote imaging spectroscopy.
Microbial communities in carbonate rocks-from soil via groundwater to rocks.

PubMed

Meier, Aileen; Singh, Manu K; Kastner, Anne; Merten, Dirk; Büchel, Georg; Kothe, Erika

2017-09-01

Microbial communities in soil, groundwater, and rock of two sites in limestone were investigated to determine community parameters differentiating habitats in two lithostratigraphic untis. Lower Muschelkalk and Middle Muschelkalk associated soils, groundwater, and rock samples showed different, but overlapping microbial communities linked to carbon fluxes. The microbial diversities in soil were highest, groundwater revealed overlapping taxa but lower diversity, and rock samples were predominantly characterized by endospore forming bacteria and few archaea. Physiological profiles could establish a differentiation between habitats (soil, groundwater, rock). From community analyses and physiological profiles, different element cycles in limestone could be identified for the three habitats. While in soil, nitrogen cycling was identified as specific determinant, in rock methanogenesis linked carbonate rock to atmospheric methane cycles. These patterns specifically allowed for delineation of lithostratigraphic connections to physiological parameters. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Calcium Isotope Fractionation during Carbonate Weathering in the Northern Guangdong, South China

NASA Astrophysics Data System (ADS)

Liu, F.; Mao, G.; Wei, G.; Zhang, Z.

2017-12-01

CO2 is consumed during the weathering of carbonates, whereas carbonates are precipitated rapidly in the oceans, which are pivotal to modulate atmospheric CO2, oceanic pH and climate. Calcium carbonate in limestone is one of the largest reservoirs of carbon at the Earth's surface, so calcium is an important element that links the lithosphere, hydrosphere, biosphere, and the atmosphere. Compared with silicate rocks, carbonate rocks have more rapid rates of physical and chemical erosions, so the carbonate weathering will respond more quickly to the climatic changes. In the southeast of China, enormous of carbonate rocks are widely distributed. Due to the influence of the subtropical monsoon climate, the rocks experienced strong chemical weathering and pedogenic process, resulting in red weathering crust of carbonate rocks. This type of weathering crust is geochemistry-sensitive and ecology-vulnerable, which can provide important insights into the recycle of supergene geochemistry in the karst areas. In this study, we report calcium isotopic compositions of saprolites from a weathering profile developed on argillaceous carbonate rocks in northern Guangdong, South China. The acid-leachable fraction, which was extracted by 1N hydrochloride acid, showed limited variation of δ44/40Ca(NIST 915a) spanning from 0.55 ± 0.06‰ (2SD) to 0.72 ± 0.05‰ (2SD) despite CaO content ranging from 0.01 wt.% to 45.7 wt.%, implying that Ca isotope didn't fractionate much which may due to the congruent dissolution of limestone minerals. In contrast, radiogenic 87Sr/86Sr ratios of the whole rocks changed with depth from 0.710086 ± 6 (2SE) at the base rock to 0.722164± 8 (2SE) at the top-soil, which are possibly attributed to the mixing effect between carbonate and silicate fractions. Sr is an analogue for Ca due to its similar ionic size and charge; however, these two systems can differ in certain respects. The coupled study of Ca and Sr will be helpful to verify sources of Ca and the global Ca and C cycles.
Microdiamonds from the European Variscan Orogenic Belt

NASA Astrophysics Data System (ADS)

Kotkova, J.; Jakubova, P.; Whitehouse, M.; Fedortchouk, Y.

2014-12-01

Diamond, along with coesite, has been discovered recently in the continental crustal rocks of the European Variscan orogenic belt, namely the Bohemian Massif (BM). In addition to the garnet-phengite gneiss in Germany, western BM, microdiamond occurs in major rock forming minerals - garnet, kyanite - and in zircon in ultrahigh-pressure rocks overprinted under high-pressure granulite facies conditions (c. 16-20 kbar, c. 1000°C) in the northern and eastern BM. Well-preserved 10-30 μm-sized microdiamonds from northern BM exhibit diverse morphologies (SEM data) depending upon the host rock type. Octahedral diamond occurs in felsic garnet-kyanite-feldspar-quartz rock (metasediment), whereas intermediate garnet-clinopyroxene-feldspar-quartz rock contains a cubo-octahedral variety. Diamond morphology can be thus controlled by solid impurities available in the medium of crystallization (K- vs. Ca-bearing fluids or melts), as shown by experiments. Pointed-bottom negatively oriented trigonal etch pits on the octahedral diamond faces developed due to diamond resorption at CO2-dominated environment (less than 50 wt % of H2O, experimental data), possibly by action of a residual fluid. SIMS determined δ13C values range from -22 to -21 ‰ for the felsic rock and from - 26 to - 33 for the intermediate one, corresponding to the typical range of organic carbon δ13C and inconsistent with a significant mantle carbon (δ13C ~ - 5 ‰) input. Diamond-bearing domains in zircon, also analysed by SIMS, yielded a Variscan U-Pb age of c. 340 Ma. The present stage of knowledge allows us to conclude that (i) metamorphic diamonds in the BM occur in lithologies of metasedimentary character, and their carbon source was organic; (ii) crustal-derived CO2-rich fluids with impurities played an important role in diamond formation and dissolution; (iii) diamonds formed during the Variscan orogenic cycle and (iv) diamonds are best preserved in the external domain of the Variscan orogenic belt.
The oxidation state of the mantle and the extraction of carbon from Earth's interior.

PubMed

Stagno, Vincenzo; Ojwang, Dickson O; McCammon, Catherine A; Frost, Daniel J

2013-01-03

Determining the oxygen fugacity of Earth's silicate mantle is of prime importance because it affects the speciation and mobility of volatile elements in the interior and has controlled the character of degassing species from the Earth since the planet's formation. Oxygen fugacities recorded by garnet-bearing peridotite xenoliths from Archaean lithosphere are of particular interest, because they provide constraints on the nature of volatile-bearing metasomatic fluids and melts active in the oldest mantle samples, including those in which diamonds are found. Here we report the results of experiments to test garnet oxythermobarometry equilibria under high-pressure conditions relevant to the deepest mantle xenoliths. We present a formulation for the most successful equilibrium and use it to determine an accurate picture of the oxygen fugacity through cratonic lithosphere. The oxygen fugacity of the deepest rocks is found to be at least one order of magnitude more oxidized than previously estimated. At depths where diamonds can form, the oxygen fugacity is not compatible with the stability of either carbonate- or methane-rich liquid but is instead compatible with a metasomatic liquid poor in carbonate and dominated by either water or silicate melt. The equilibrium also indicates that the relative oxygen fugacity of garnet-bearing rocks will increase with decreasing depth during adiabatic decompression. This implies that carbon in the asthenospheric mantle will be hosted as graphite or diamond but will be oxidized to produce carbonate melt through the reduction of Fe(3+) in silicate minerals during upwelling. The depth of carbonate melt formation will depend on the ratio of Fe(3+) to total iron in the bulk rock. This 'redox melting' relationship has important implications for the onset of geophysically detectable incipient melting and for the extraction of carbon dioxide from the mantle through decompressive melting.
Mars Mineralogy by Microbeam Raman Spectrometry

NASA Technical Reports Server (NTRS)

Haskin, Larry A.; Wang, Alian; Jolliff, Bradley L.; Wdowiak, Thomas J.; Agresti, David G.; Lane, Arthur L.; Squyres, Steven W.

2001-01-01

The Mars Microbeam Raman Spectrometer, under development at Washington University and the Jet Propulsion Laboratory, can identify oxide, sulfide, and oxyanion minerals, bound water and OH, and organic and graphitic carbon in Mars rocks and soils in situ. Additional information is contained in the original extended abstract.
The origin, type and hydrocarbon generation potential of organic matter in a marine-continental transitional facies shale succession (Qaidam Basin, China).

PubMed

Wang, Guo-Cang; Sun, Min-Zhuo; Gao, Shu-Fang; Tang, Li

2018-04-26

This organic-rich shale was analyzed to determine the type, origin, maturity and depositional environment of the organic matter and to evaluate the hydrocarbon generation potential of the shale. This study is based on geochemical (total carbon content, Rock-Eval pyrolysis and the molecular composition of hydrocarbons) and whole-rock petrographic (maceral composition) analyses. The petrographic analyses show that the shale penetrated by the Chaiye 2 well contains large amounts of vitrinite and sapropelinite and that the organic matter within these rocks is type III and highly mature. The geochemical analyses show that these rocks are characterized by high total organic carbon contents and that the organic matter is derived from a mix of terrestrial and marine sources and highly mature. These geochemical characteristics are consistent with the results of the petrographic analyses. The large amounts of organic matter in the Carboniferous shale succession penetrated by the Chaiye 2 well may be due to good preservation under hypersaline lacustrine and anoxic marine conditions. Consequently, the studied shale possesses very good hydrocarbon generation potential because of the presence of large amounts of highly mature type III organic matter.
Publications - RDF 2005-2 | Alaska Division of Geological & Geophysical

Science.gov Websites

, and non-carbonate carbon data from rocks collected in the Solomon, Bendeleben, and Nome quadrangles for more information. Quadrangle(s): Bendeleben; Nome; Solomon Bibliographic Reference Werdon, M.B , geochemical, and non-carbonate carbon data from rocks collected in the Solomon, Bendeleben, and Nome
Sulfur and carbon geochemistry of the Santa Elena peridotites: Comparing oceanic and continental processes during peridotite alteration

NASA Astrophysics Data System (ADS)

Schwarzenbach, Esther M.; Gill, Benjamin C.; Gazel, Esteban; Madrigal, Pilar

2016-05-01

Ultramafic rocks exposed on the continent serve as a window into oceanic and continental processes of water-peridotite interaction, so called serpentinization. In both environments there are active carbon and sulfur cycles that contain abiogenic and biogenic processes, which are eventually imprinted in the geochemical signatures of the basement rocks and the calcite and magnesite deposits associated with fluids that issue from these systems. Here, we present the carbon and sulfur geochemistry of ultramafic rocks and carbonate deposits from the Santa Elena ophiolite in Costa Rica. The aim of this study is to leverage the geochemistry of the ultramafic sequence and associated deposits to distinguish between processes that were dominant during ocean floor alteration and those dominant during low-temperature, continental water-peridotite interaction. The peridotites are variably serpentinized with total sulfur concentrations up to 877 ppm that is typically dominated by sulfide over sulfate. With the exception of one sample the ultramafic rocks are characterized by positive δ34Ssulfide (up to + 23.1‰) and δ34Ssulfate values (up to + 35.0‰). Carbon contents in the peridotites are low and are isotopically distinct from typical oceanic serpentinites. In particular, δ13C of the inorganic carbon suggests that the carbon is not derived from seawater, but rather the product of the interaction of meteoric water with the ultramafic rocks. In contrast, the sulfur isotope data from sulfide minerals in the peridotites preserve evidence for interaction with a hydrothermal fluid. Specifically, they indicate closed system abiogenic sulfate reduction suggesting that oceanic serpentinization occurred with limited input of seawater. Overall, the geochemical signatures preserve evidence for both oceanic and continental water-rock interaction with the majority of carbon (and possibly sulfate) being incorporated during continental water-rock interaction. Furthermore, there is evidence for microbial activity that was possibly stimulated by carbon sourced from water-rock interaction with adjacent sediments or fluid inclusions. This study provides detailed insight into the complex hydrothermal history of continental serpentinization systems and adds to our understanding of the carbon and sulfur cycling within peridotite-hosted hydrothermal systems.
The story of Amazonian climate change on Mars as told by carbonates in Miller Range Nakhlites

NASA Astrophysics Data System (ADS)

Evans, M. E.; Niles, P. B.; Locke, D.; Chapman, P.

2017-12-01

This is a story about rocks from Mars, and how they reveal environmental changes on Mars. A specific region of volcanic rocks formed on Mars about 1.3 billion years ago (bya). This region is now known as the Nakhla lava pile. The rocks were likely formed near the surface. Chemical analysis of these rocks confirms that they formed on Mars, because rocks on Earth have different oxygen isotope values. Sometime later, perhaps 0.7 bya, very small amounts of subsurface water on Mars percolated through the lava pile. The water contained dissolved carbon dioxide (CO2) from contact with the atmosphere of Mars. Ions in the water bonded with rock ions to create tiny, white, carbonate minerals along the cracks within the lava pile. The Nakhla subsurface water temperature was likely cool ( 15°C), which is different from the hot water that possibly created minerals on older Mars rocks. About 11 million years ago, an asteroid impacted Mars over the Nakhla lava pile. The impact rebound ejected mass from the surface and subsurface, and some rocks escaped the gravity of Mars. These rocks floated in space for over 10.9 million years before they fell to Earth as meteorites. The most famous of these meteorites, named Nakhla, fell over Egypt in 1911 and fragmented into 40 pieces. A total of 11 similar meteorites, known as Nakhlites, have been collected across the Earth. Four of these meteorites fell into a remote region of Antarctica called the Miller Range (MIL). They were collected by the National Science Foundation (NSF) "Antarctica Search for Meteorite" (ANSMET) program. This study analyzed the stable isotope geochemistry of the carbonates on the four MIL Nakhlites. Antarctica is an analog for carbonate formation on recent Mars because it forms the minerals in a cold environment with a thin film of water. Carbonates from oceans are dominated by the oxygen isotopic values of the water, but in Mars and Antarctica the carbonates are also influenced by the oxygen in the atmospheric CO2. This study reveals that terrestrial carbonates have different carbon isotope values from martian carbonates. The carbon isotope values of the Mars atmospheric CO2 that formed the MIL Nakhlite carbonates was different from the modern atmosphere (as measured by the MSL Curiosity rover). This difference may be due somewhat to loss of atmospheric gas to space over the past billion years.
Laboratory Experiments to Evaluate Matrix Diffusion of Dissolved Organic Carbon Carbon-14 in Southern Nevada Fractured-rock Aquifers

DOE Office of Scientific and Technical Information (OSTI.GOV)

Hershey, Ronald L.; Fereday, Wyatt

Dissolved inorganic carbon (DIC) carbon-14 ( 14C) is used to estimate groundwater ages by comparing the DIC 14C content in groundwater in the recharge area to the DIC 14C content in the downgradient sampling point. However, because of chemical reactions and physical processes between groundwater and aquifer rocks, the amount of DIC 14C in groundwater can change and result in 14C loss that is not because of radioactive decay. This loss of DIC 14C results in groundwater ages that are older than the actual groundwater ages. Alternatively, dissolved organic carbon (DOC) 14C in groundwater does not react chemically with aquifermore » rocks, so DOC 14C ages are generally younger than DIC 14C ages. In addition to chemical reactions, 14C ages may also be altered by the physical process of matrix diffusion. The net effect of a continuous loss of 14C to the aquifer matrix by matrix diffusion and then radioactive decay is that groundwater appears to be older than it actually is. Laboratory experiments were conducted to measure matrix diffusion coefficients for DOC 14C in volcanic and carbonate aquifer rocks from southern Nevada. Experiments were conducted using bromide (Br-) as a conservative tracer and 14C-labeled trimesic acid (TMA) as a surrogate for groundwater DOC. Outcrop samples from six volcanic aquifers and five carbonate aquifers in southern Nevada were used. The average DOC 14C matrix diffusion coefficient for volcanic rocks was 2.9 x 10 -7 cm 2/s, whereas the average for carbonate rocks was approximately the same at 1.7 x 10 -7 cm 2/s. The average Br- matrix diffusion coefficient for volcanic rocks was 10.4 x 10 -7 cm 2/s, whereas the average for carbonate rocks was less at 6.5 x 10 -7 cm 2/s. Carbonate rocks exhibited greater variability in DOC 14C and Br- matrix diffusion coefficients than volcanic rocks. These results confirmed, at the laboratory scale, that the diffusion of DOC 14C into southern Nevada volcanic and carbonate aquifers is slower than DIC 14C. Because of the apparent sorption of 14C-labeled TMA in the experiments, matrix diffusion coefficients are likely even lower. The reasons for the higher than expected Br-/ 14C-labeled TMA are unknown. Because the molecular size of TMA is on the low end of the range in molecular size for typical humic substances, the matrix diffusion coefficients for the 14C-labeled TMA likely represent close to the maximum diffusion rates for DOC 14C in the volcanic and carbonate aquifers in southern Nevada.« less
Depositional setting and diagenetic evolution of some Tertiary unconventional reservoir rocks, Uinta Basin, Utah.

USGS Publications Warehouse

Pitman, Janet K.; Fouch, T.D.; Goldhaber, M.B.

1982-01-01

The Douglas Creek Member of the Tertiary Green River Formation underlies much of the Uinta basin, Utah, and contains large volumes of oil and gas trapped in a complex of fractured low-permeability sandstone reservoirs. In the SE part of the basin at Pariette Bench, the Eocene Douglas Creek Member is a thick sequence of fine- grained alluvial sandstone complexly intercalated with lacustrine claystone and carbonate rock. Sediments were deposited in a subsiding intermontane basin along the shallow fluctuating margin of ancient Lake Uinta. Although the Uinta basin has undergone postdepositional uplift and erosion, the deepest cored rocks at Pariette Bench have never been buried more than 3000m.-from Authors
Regional stratigraphic framework of the Lisburne Group of ANWR

DOE Office of Scientific and Technical Information (OSTI.GOV)

Watts, K.F.; Carlson, R.C.; Harris, A.G.

1995-05-01

The Carboniferous Lisburne Group, a major carbonate platform succession, is widely exposed in the Brooks Range and forms an extensive hydrocarbon target in the subsurface of the North Slope of Alaska. Gradationally beneath carbonates of the Lisburne Group, terrigenous sediments of the Mississippian Endicott Group (conglomerate and sandstone of the Kekiktuk Formation overlain by the Kayak Shale) were derived from local and northern (Ellesmerian) source areas. Locally, at the Endicott-Lisburne transition, sandy limestones of the Itkilyariak Formation record another phase of siliciclastic influx that lies above and/or is a lateral equivalent of the Kayak Shale and Lisburne Group in areasmore » adjacent to paleotopographic highs. This siliciclastic to carbonate transition represents a major transgressive succession that onlaps northward over the sub-Mississippian unconformity, a regional angular unconformity and sequence boundary in northern Alaska. The age and nature of onlap depend upon the paleotopography of the underlying sub-Mississippian rocks and regional passive margin subsidence. The Lisburne Group is a thick succession of carbonate rocks subdivided into the Alapah Limestone and overlying Wahoo Limestone, both having informal members.« less
Mapping the Mineral Resource Base for Mineral Carbon-Dioxide Sequestration in the Conterminous United States

USGS Publications Warehouse

Krevor, S.C.; Graves, C.R.; Van Gosen, B. S.; McCafferty, A.E.

2009-01-01

This database provides information on the occurrence of ultramafic rocks in the conterminous United States that are suitable for sequestering captured carbon dioxide in mineral form, also known as mineral carbon-dioxide sequestration. Mineral carbon-dioxide sequestration is a proposed greenhouse gas mitigation technology whereby carbon dioxide (CO2) is disposed of by reacting it with calcium or magnesium silicate minerals to form a solid magnesium or calcium carbonate product. The technology offers a large capacity to permanently store CO2 in an environmentally benign form via a process that takes little effort to verify or monitor after disposal. These characteristics are unique among its peers in greenhouse gas disposal technologies. The 2005 Intergovernmental Panel on Climate Change report on Carbon Dioxide Capture and Storage suggested that a major gap in mineral CO2 sequestration is locating the magnesium-silicate bedrock available to sequester the carbon dioxide. It is generally known that silicate minerals with high concentrations of magnesium are suitable for mineral carbonation. However, no assessment has been made in the United States that details their geographical distribution and extent, nor has anyone evaluated their potential for use in mineral carbonation. Researchers at Columbia University and the U.S. Geological Survey have developed a digital geologic database of ultramafic rocks in the conterminous United States. Data were compiled from varied-scale geologic maps of magnesium-silicate ultramafic rocks. The focus of our national-scale map is entirely on ultramafic rock types, which typically consist primarily of olivine- and serpentine-rich rocks. These rock types are potentially suitable as source material for mineral CO2 sequestration.
Carbonation of Peridotite by CO2-rich Fluids: Insights from Listvenites in the Advocate Ophiolite (Newfoundland)

NASA Astrophysics Data System (ADS)

Menzel, Manuel; Garrido, Carlos J.; Marchesi, Claudio; López Sánchez Vizcaíno, Vicente; Hidas, Károly; Escayola, Monica P.; Jamtveit, Bjørn

2017-04-01

Listvenites are the result of a sequence of reactions of CO2-rich hydrothermal fluids with serpentinite that forms magnesite-quartz rocks in the last reaction step. Listvenites are natural analogues for carbon sequestration by mineral carbonation, fixing large quantities of carbon in relatively small, confined zones of intense reactive fluid flux within serpentinite. The association of listvenite (magnesite-quartz), soapstone (talc-magnesite) and carbonated serpentinite in the mantle section of the Advocate ophiolite complex in Newfoundland (Canada) is an ideal natural example to study the carbonation of serpentinites because the reaction progress is recorded by the differently carbonated assemblages. The Advocate listvenites crop out in a 20-30 m wide zone that can be followed for about 1 km, surrounded by serpentinite and harzburgite. Quartz and magnesite veins are widespread in the central listvenite domain. This mobilization of silica into a vein network is reflected in a depletion of silica in the most carbonated lithologies, whereas most other major elements remain unchanged over a wide range of CO2-contents. Notably, there is a sharp decrease in bulk rock Fe3+/Fetotal from 0.65 - 0.8 in lizardite-chrysotile serpentinites to 0.1 - 0.3 in talc-magnesite rocks and listvenites. High Cr and Ni contents and preserved red-brown Cr-spinel in the carbonated lithologies demonstrate the mantle peridotites provenance of the listvenites. The presence of thin veins of Cr-mica (fuchsite) suggests that Cr was mobilized to some degree. Fine dispersed magnetite trails in magnesite trace serpentine pseudomorphs after olivine, indicating that no deformation occurred in some domains during the carbonation, while deformation was concentrated in talc-rich lithologies. The rheological contrasts of serpentinites, soapstones and listvenites and, in consequence, the formation of veins in response to shear- or extensional fractures may result in a re-opening of pathways for the influx of very CO2-rich fluids that are needed for the formation of listvenites. Carbonated mantle rocks like the Advocate listvenites may represent the best accessible natural analogue for carbonation of serpentinites through bend faulting at the outer rise of trenches, since hydrothermal fluids in those systems may become more CO2-rich due to percolation through overlying sediments, thus allowing for localized intense carbonation. Funding: We acknowledge funding from the People programme (Marie Curie Actions - ITN) of the European Union FP7 under REA Grant Agreement n˚ 608001.
Nanoindentation of dry and fluid-saturated micro-porous rocks

NASA Astrophysics Data System (ADS)

Mighani, S.; Bernabe, Y.; Schwartzman, A. F.; Evans, J. B.

2017-12-01

In this report we explore the ability of nanoindentation technique to evaluate the pore-scale solid-fluid interactions in micro-porous rocks. We measure the creep deformation of a porous rock sample over a period of 3 minutes under a constant maximum force. The indentation tip is instrumented with a nano-DMA transducer which efficiently compensates for the thermal drifts. The candidate rock is a carbonate with micro-porous micritic cement. Secondary Electron (SE) images revealed a bimodal pore structure for this rock-type: regions (A) of micritic cement with micropores, and (B) with large grains and vuggy pores. The experiments were performed on dry rock samples as well as saturated with water (1 cp and buffered with 30 ppm calcite powder) and silicone oil (100 cp). Thus, the fluids presented a wide variation in viscosity and chemical reactivity. We then explored the size (maximum forces of 2, 4, and 8 mN) and loading rate (0.2-2 mN/sec) dependency of the observed creep behavior. The amount of total deformation within the 3 minutes of creep showed a uniform increase with a tendency to reach an equilibrium depth with creep rates (dh/h) below 5×10-3. The indentations in the water-saturated carbonate showed a 6-fold decrease in the Young's modulus (from 38 to 6 GPa) and 2-fold increase in creep magnitude (from 59 to 119 nm) compared with the dry indentations. We attribute these large differences to the possible chemical reaction of water and carbonate. This is further confirmed by comparing the hardness values, which showed that water softened the rock matrix by a factor of 4 (from 0.87 to 0.22 GPa). The carbonate sample saturated with oil, on the other hand, showed a higher modulus (47 GPa) and greater hardness (1.39 GPa), while the creep magnitude (31 nm) was half that observed in dry rock. We attribute this behavior to the viscous displacement of the pore fluid during consolidation of the poroelastic matrix. The loading rate-dependency and size (maximum load) sensitivity of the observed creep appear consistent with poroelasticity. We used Agbezuge and Deresiewicz's (1974) solution to derive poroelastic constants based on the recorded amount of creep. The analysis yields estimates of the diffusivity constant of the rock and the equilibrium creep depth. (We would like to acknowledge The U.S. Department of Energy (DOE) for their support)

Validating predictions of evolving porosity and permeability in carbonate reservoir rocks exposed to CO2-brine

NASA Astrophysics Data System (ADS)

Smith, M. M.; Hao, Y.; Carroll, S.

2017-12-01

Improving our ability to better forecast the extent and impact of changes in porosity and permeability due to CO2-brine-carbonate reservoir interactions should lower uncertainty in long-term geologic CO2 storage capacity estimates. We have developed a continuum-scale reactive transport model that simulates spatial and temporal changes to porosity, permeability, mineralogy, and fluid composition within carbonate rocks exposed to CO2 and brine at storage reservoir conditions. The model relies on two primary parameters to simulate brine-CO2-carbonate mineral reaction: kinetic rate constant(s), kmineral, for carbonate dissolution; and an exponential parameter, n, relating porosity change to resulting permeability. Experimental data collected from fifteen core-flooding experiments conducted on samples from the Weyburn (Saskatchewan, Canada) and Arbuckle (Kansas, USA) carbonate reservoirs were used to calibrate the reactive-transport model and constrain the useful range of k and n values. Here we present the results of our current efforts to validate this model and the use of these parameter values, by comparing predictions of extent and location of dissolution and the evolution of fluid permeability against our results from new core-flood experiments conducted on samples from the Duperow Formation (Montana, USA). Agreement between model predictions and experimental data increase our confidence that these parameter ranges need not be considered site-specific but may be applied (within reason) at various locations and reservoirs. This work was performed under the auspices of the U.S. Department of Energy by Lawrence Livermore National Laboratory under Contract DE-AC52-07NA27344.
Effect of annealing on the structural and optical properties of heavily carbon-doped ZnO

NASA Astrophysics Data System (ADS)

Huang, He; Deng, Z. W.; Li, D. C.; Barbir, E.; Y Jiang, W.; Chen, M. X.; Kavanagh, K. L.; Mooney, P. M.; Watkins, S. P.

2010-04-01

ZnO films grown by metalorganic vapor phase epitaxy (MOVPE) at low temperatures (~500 °C) exhibit very high levels of carbon incorporation in the range of up to several percent. Such large levels of carbon incorporation significantly affect the structural properties of the thin films resulting in broadening of symmetric (0 0 2) rocking curves as well as broadened (1 0 1) pole figures compared with films grown at high temperature. Annealing of the films under air ambient at temperatures between 800 and 1100 °C results in dramatic sharpening of symmetric (0 0 2) rocking curves, indicating improved crystal alignment along the c-axes. (1 0 1) pole figure scans also show significant sharpening in the azimuthal axis, indicating similar improvements in the in-plane crystal alignment perpendicular to the c-axis. Raman spectra for as-grown ZnO at 500 °C show strong D and G peaks at 1381 and 1578 cm-1 due to sp2 carbon clusters. Annealing at 1000 °C results in the elimination of these bands, indicating that post-growth annealing treatment is a useful method to reduce the concentration of sp2 carbon clusters.
Investigating Interactions between the Silica and Carbon Cycles during Precipitation and Early Diagenesis of Authigenic Clay/Carbonate-Mineral Associations in the Carbonate Rock Record

NASA Astrophysics Data System (ADS)

McKenzie, J. A.; Francisca Martinez Ruiz, F.; Sanchez-Roman, M.; Anjos, S.; Bontognali, T. R. R.; Nascimento, G. S.; Vasconcelos, C.

2017-12-01

The study of authigenic clay/carbonate-mineral associations within carbonate sequences has important implications for the interpretation of scientific problems related with rock reservoir properties, such as alteration of potential porosity and permeability. More specifically, when clay minerals are randomly distributed within the carbonate matrix, it becomes difficult to predict reservoir characteristics. In order to understand this mineral association in the geological record, we have undertaken a comparative study of specially designed laboratory experiments with modern environments, where clay minerals have been shown to precipitate together with a range of carbonate minerals, including calcite, Mg-calcite and dolomite. Two modern dolomite-forming environments, the Coorong lakes, South Australia and Brejo do Espinho Rio de Janeiro, Brazil, were selected for this investigation. For comparative evaluation, enrichment microbial culture experiments, using natural pore water from Brejo do Espinho as the growth medium to promote mineral precipitation, were performed under both aerobic and anaerobic conditions. To establish the environmental parameters and biological processes facilitating the dual mineral association, the experimental samples have been compared with the natural minerals using HRTEM measurements. The results demonstrate that the clay and carbonate minerals apparently do not co-precipitate, but the precipitation of the different minerals in the same sample has probably occurred under different environmental conditions with variable chemistries, e.g., hypersalinity versus normal salinity resulting from the changing ratio of evaporation versus precipitation. Thus, the investigated mineral association is not a product of diagenetic processes but of sequential in situ precipitation processes related to changes in the silica and carbon availability. Implications for ancient carbonate formations will be presented and discussed in the context of a specific example of this clay/carbonate-mineral association recorded in the Lower Cretaceous Codó Formation, NE Brazil (Bahniuk et al., 2015. Sedimentology, 62, 155-181).
Geologic setting of the Mountain Pass rare earth deposits, San Bernardino County, California

USGS Publications Warehouse

Olson, Jerry Chipman

1952-01-01

The Mountain Pass district is in a block of pre-Cambrian metamorphic rocks bounded on the east and south by the alluvium of Ivanpah Valley. This block is separated from Paleozoic and Mesozoic sedimentary and volcanic rocks on the west by the Clark Mountain normal fault, and the northern boundary of the district is a prominent transverse fault. The pre-Cambrian metamorphic complex comprises a great variety of lithologic types including garnetiferous mica gneisses and schists; biotite-garnet-sillimenite gneiss; hornblende gneiss, schist, and amphibolite; biotite gneiss and schist; granitic gneisses and migmatites; pegmatites; and minor amounts of foliated mafic rocks. The rare earth-bearing carbonate rocks are related to potash-rich igneous rocks, of uncertain age, that cut the metamorphic complex. The larger potash-rich intrusive masses, 300 or more feet wide, comprise one granite, two syenite, and four composite shonkinite-syenite bodies. One of the shonkinite-syenite stocks is more than a mile long. Several hundred relatively thin dikes of these potash-rich rocks range in composition, and generally decreasing age, from biotite shonkinite through syenite to granite. A few thin fine-grained shonkinite dikes cut the granite. These potash-rich rocks are cut by east-trending andesitic dikes and by faults. Veins of carbonate rock are most abundant in and near the southwest side of the largest shonkinite-syenite body. Although most veins are less than 6 feet thick, one mass of carbonate rock near the Sulphide Queen min4e is 600 feet in maximum width and 2,400 feet long. About 200 veins have been mapped in the district; their aggregate surface area is probably less than one-tenth that of the large carbonate mass. The carbonate materials, which make up about 60 percent of the veins and the large carbonite body, are chiefly calcite, dolomite, ankerite, and siderite. The other constituents are barite, bastnaesite and perisite, quartz, and variable small quantities of crocidolite, biotite, phlogopite, chlorite, muscovite, apatite, iron oxides, fluorite, monazite, galena, allanite, sphene, pyrite, chalcopyrite, tetrahedrite, malachite, azurite, corussite, wulfenite, aragonite, and thorite. The rare earth oxide content in most of the carbonate rock is less than 13 percent, but in some local concentrations of bastnaesite the content is as high as 40 percent. The origin of the carbonate rocks and related potash-rich igneous rocks is considered in the light of similar associations of carbonate and alkalinic rocks in Sweden, Norway, Russia, South Africa, and the United States. The carbonate rock may have originated (1) as a pre-Cambrian limestone or evaporate sequence in the gneisses; (2) by reaction between magma and the Paleozoic dolomite and limestone overlying the pre-Cambrian complex; (3) by alteration of pre-Cambrian gneisses by emanations from an unknown deep-seated source; or (4) by differentiation of an alkaline magma from shonkinite to syenite to granite, leading to a final carbonate-rich fraction, containing the rare elements, which was emplaced either as a concentrated or a dilute solution. The fourth hypothesis is considered the most plausible.
Publications - RDF 2007-4 | Alaska Division of Geological & Geophysical

Science.gov Websites

, and non-carbonate carbon data from rocks collected in the Solomon and Nome quadrangles, Seward information. Quadrangle(s): Nome; Solomon Bibliographic Reference Werdon, M.B., Newberry, R.J., Szumigala, D.J -carbonate carbon data from rocks collected in the Solomon and Nome quadrangles, Seward Peninsula, Alaska in
Hydrogeology of south-central St Croix, US Virgin Islands

USGS Publications Warehouse

Graves, R.P.

1995-01-01

The subsurface geology of south-central St. Croix consists of alluvium and underlying carbonate rocks. The alluvial deposits consist of sand and gravel with cobbles and boulders and, locally, thin lenses of silt and clay. The carbonate rocks consist of the Oligocene to Middle Miocene age Jealousy formation, the Miocene and Pliocene are Kingshill Limestone, and the Pliocene and younger age Post-Kingshill Carbonates. Ground water occurs under water-table conditions in the alluvial, Post-Kingshill Carbonates, and Kingshill Limestone deposits. These deposits are hydraulically connected and are considered to be a single hydrologic unit. The top of the water-table aquifer can range from 5 to 68 feet below land surface. The top of the Jealousy Formation is considered to be the bottom of the water- table aquifer and generally is from 85 to greater than 120 feet below land surface. Aquifer yields in south- central St. Croix can range from less than 5 gallons per minute to 80 gallons per minute. The ground- water in the study area is of the sodium-chloride type. Ground-water samples collected from selected wells had chloride concentrations ranging from 64 to 4,400 milligrams per liter, and dissolved solid concen- trations ranging from 619 to 7,540 milligrams per liter. Connate water is suspected as being the source of sodium chloride in the ground water.
Clumped-isotope thermometry of magnesium carbonates in ultramafic rocks

DOE PAGES

Garcia del Real, Pablo; Maher, Kate; Kluge, Tobias; ...

2016-08-19

Here, magnesium carbonate minerals produced by reaction of H 2O–CO 2 with ultramafic rocks occur in a wide range of paragenetic and tectonic settings and can thus provide insights into a variety of geologic processes, including deposition of ore-grade, massive-vein cryptocrystalline magnesite; formation of hydrous magnesium carbonates in weathering environments; and metamorphic carbonate alteration of ultramafic rocks. However, the application of traditional geochemical and isotopic methods to infer temperatures of mineralization, the nature of mineralizing fluids, and the mechanisms controlling the transformation of dissolved CO 2 into magnesium carbonates in these settings is difficult because the fluids are usually notmore » preserved.« less
Clumped-isotope thermometry of magnesium carbonates in ultramafic rocks

DOE Office of Scientific and Technical Information (OSTI.GOV)

Garcia del Real, Pablo; Maher, Kate; Kluge, Tobias

Here, magnesium carbonate minerals produced by reaction of H 2O–CO 2 with ultramafic rocks occur in a wide range of paragenetic and tectonic settings and can thus provide insights into a variety of geologic processes, including deposition of ore-grade, massive-vein cryptocrystalline magnesite; formation of hydrous magnesium carbonates in weathering environments; and metamorphic carbonate alteration of ultramafic rocks. However, the application of traditional geochemical and isotopic methods to infer temperatures of mineralization, the nature of mineralizing fluids, and the mechanisms controlling the transformation of dissolved CO 2 into magnesium carbonates in these settings is difficult because the fluids are usually notmore » preserved.« less
Wave Velocities in Hydrocarbons and Hydrocarbon Saturated - Applications to Eor Monitoring.

NASA Astrophysics Data System (ADS)

Wang, Zhijing

In order to effectively utilize many new seismic technologies and interpret the results, acoustic properties of both reservoir fluids and rocks must be well understood. It is the main purpose of this dissertation to investigate acoustic wave velocities in different hydrocarbons and hydrocarbon saturated rocks under various reservoir conditions. The investigation consists of six laboratory experiments, followed by a series of theoretical and application analyses. All the experiments involve acoustic velocity measurements in hydrocarbons and rocks with different hydrocarbons, using the ultrasonic pulse-transmission methods, at elevated temperatures and pressures. In the experiments, wave velocities are measured versus both temperature and pressure in 50 hydrocarbons. The relations among the acoustic velocity, temperature, pressure, API gravity, and the molecular weight of the hydrocarbons are studied, and empirical equations are established which allow one to calculate the acoustic velocities in hydrocarbons with known API gravities. Wave velocities in hydrocarbon mixtures are related to the composition and the velocities in the components. The experimental results are also analyzed in terms of various existing theories and models of the liquid state. Wave velocities are also measured in various rocks saturated with different hydrocarbons. The compressional wave velocities in rocks saturated with pure hydrocarbons increase with increasing the carbon number of the hydrocarbons. They decrease markedly in all the heavy hydrocarbon saturated rocks as temperature increases. Such velocity decreases set the petrophysical basis for in-situ seismic monitoring thermal enhanced oil recovery processes. The effects of carbon dioxide flooding and different pore fluids on wave velocities in rocks are also investigated. It is highly possible that there exist reflections of seismic waves at the light-heavy oil saturation interfaces in-situ. It is also possible to use seismic methods to monitor carbon dioxide flooding processes. Velocity dispersions are analyzed theoretically in rocks saturated with different pore fluids. The results are discussed in terms of the Biot theory and the "local flow" mechanism. Applications of the results and the applicability of using seismic methods to monitor various enhanced oil recovery and production processes are also discussed.
Publications - GMC 137 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 137 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Reference Unknown, 1989, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance data of Report Report Information gmc137.pdf (47.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic
Publications - GMC 141 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 141 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Reference Unknown, 1989, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance data of Report Report Information gmc141.pdf (70.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic
Publications - GMC 68 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 68 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Reference Unknown, 1987, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance geochemical Report Report Information gmc068.pdf (48.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic
Carbonate Melt Rocks from the Haughton Impact Structure, Devon Island, Nunavut, Canada

NASA Technical Reports Server (NTRS)

Osinski, G. R.; Spray, J. G.; Lee, P.

2002-01-01

The target rocks at the Haughton impact structure, Canada, are predominantly carbonates. The well preserved allochthonous crater-fill deposits are reinterpreted here as being carbonatitic impact melt rocks. The implications of our findings will be discussed. Additional information is contained in the original extended abstract.
NMR permeability estimators in 'chalk' carbonate rocks obtained under different relaxation times and MICP size scalings

NASA Astrophysics Data System (ADS)

Rios, Edmilson Helton; Figueiredo, Irineu; Moss, Adam Keith; Pritchard, Timothy Neil; Glassborow, Brent Anthony; Guedes Domingues, Ana Beatriz; Bagueira de Vasconcellos Azeredo, Rodrigo

2016-07-01

The effect of the selection of different nuclear magnetic resonance (NMR) relaxation times for permeability estimation is investigated for a set of fully brine-saturated rocks acquired from Cretaceous carbonate reservoirs in the North Sea and Middle East. Estimators that are obtained from the relaxation times based on the Pythagorean means are compared with estimators that are obtained from the relaxation times based on the concept of a cumulative saturation cut-off. Select portions of the longitudinal (T1) and transverse (T2) relaxation-time distributions are systematically evaluated by applying various cut-offs, analogous to the Winland-Pittman approach for mercury injection capillary pressure (MICP) curves. Finally, different approaches to matching the NMR and MICP distributions using different mean-based scaling factors are validated based on the performance of the related size-scaled estimators. The good results that were obtained demonstrate possible alternatives to the commonly adopted logarithmic mean estimator and reinforce the importance of NMR-MICP integration to improving carbonate permeability estimates.
Carbonation of mantle peridotites: implications for permanent geological CO2 capture and storage

NASA Astrophysics Data System (ADS)

Paukert, A. N.; Matter, J. M.; Kelemen, P. B.; Marsala, P.; Shock, E.

2012-12-01

In situ carbonation of mantle peridotites serves as a natural analog to engineered mineral carbonation for geological CO2 capture and storage. For example, mantle peridotite in the Samail Ophiolite, Oman naturally captures and stores about 5x104 tons of atmospheric CO2 per year as carbonate minerals, and has been doing so for the past 50,000 years [Kelemen et al., 2011]. Our reaction path modeling of this system shows that the natural process is limited by subsurface availability of dissolved inorganic carbon, and that the rate of CO2 mineralization could be enhanced by a factor of 16,000 by injecting CO2 into the peridotite aquifer at 2 km depth and a fugacity of 100 bars. Injecting CO2 into mafic or ultramafic rock formations has been presumed difficult, as fractured crystalline rocks typically have low porosity and permeability; however these factors have yet to be comprehensively studied. To determine the actual value of these hydrogeological factors, this winter we carried out a multifaceted study of deep boreholes (up to 350m) in the mantle peridotite and the Moho transition zone of the Samail Ophiolite. A suite of physical and chemical parameters were collected, including slug tests for hydraulic conductivity, geophysical well logs for porosity and hydraulic conductivity, drill chips for extent and composition of secondary mineralization, and water and dissolved gas samples for chemical composition. All of these factors combine to provide a comprehensive look at the chemical and physical processes underlying natural mineral carbonation in mantle peridotites. Understanding the natural process is critical, as mineral carbonation in ultramafic rocks is being explored as a permanent and relatively safe option for geologic carbon sequestration. While injectivity in these ultramafic formations was believed to be low, our slug test and geophysical well log data suggest that the hydraulic conductivity of fractured peridotites can actually be fairly high - up to meters/day, on par with fine to medium grained sandstones - so these formations may be more suitable than previously thought. Using the Samail Ophiolite as a natural analog for in situ mineral carbonation in ultramafic rocks should help predict and optimize the efficacy and security of engineered CO2 storage projects.
Lithology of the basement underlying the Campi Flegrei caldera: Volcanological and petrological constraints

NASA Astrophysics Data System (ADS)

D'Antonio, Massimo

2011-02-01

A geologically reasonable working hypothesis is proposed for the lithology of the basement underlying the Campi Flegrei caldera in the ca. 4-8 km depth range. In most current geophysical modeling, this portion of crust is interpreted as composed of Meso-Cenozoic carbonate rocks, underlain by a ca. 1 km thick sill of partially molten rock, thought to be a main magma reservoir. Shallower magma reservoirs likely occur in the 3-4 km depth range. However, the lack of carbonate lithics in any Campi Flegrei caldera volcanic rocks does not support the hypothesis of a limestone basement. Considering the major caldera-forming eruptions, which generated widespread and voluminous ignimbrites during late Quaternary times, including the Campanian Ignimbrite and Neapolitan Yellow Tuff eruptions, the total volume of trachytic to phonolitic ejected magma is conservatively estimated at not less than 350 km 3. Results of least-squared mass-balance calculations suggest that this evolved magma formed through fractional crystallization from at least 2500 km 3 of parent shoshonitic magma, in turn derived from even more voluminous, more mafic, K-basaltic magma. Calculations suggest that shoshonitic magma, likely emplaced at ca. 8 km depth, must have crystallized about 2100 km 3 of solid material, dominated by alkali-feldspar and plagioclase, with a slightly lower amount of mafic minerals, during its route toward shallower magma reservoirs, before feeding the Campi Flegrei large-volume eruptions. The calculated volume of cumulate material, likely syenitic in composition at least in its upper portions, is more than enough to completely fill the basement volume in the 4-8 km depth range beneath the Campi Flegrei caldera, estimated at ca. 1250 km 3. Thus, it is proposed that the basement underlying the Campi Flegrei caldera below 4 km is composed mostly of crystalline igneous rocks, as for many large calderas worldwide. Syenite sensu lato would meet physical properties requirements for geophysical data interpretations, explain some geochemical and isotopic features of the past 15 ka volcanics, and justify the carbon isotopic composition of fumaroles at the Campi Flegrei caldera. This implies that Meso-Cenozoic limestones, if still present today beneath the Campi Flegrei caldera, no longer constitute significant portions of its basement.
Impact of hydrothermal alteration on time-dependent tunnel deformation in Neogene volcanic rock sequence in Japan: Petrology, Geochemistry and Geophysical investigation

NASA Astrophysics Data System (ADS)

Yamazaki, S.; Okazaki, K.; Niwa, H.; Arai, T.; Murayama, H.; Kurahashi, T.; Ito, Y.

2017-12-01

Time-dependent tunnel deformation is one of remaining geological problems for mountain tunneling. As a case study of time-dependent tunnel deformation, we investigated petrographical, mineral and chemical compositions of boring core samples and seismic exploration along a tunnel that constructed into Neogene volcanic rock sequence of andesite to dacite pyroclastic rocks and massive lavas with mafic enclaves. The tunnel has two zones of floor heaving that deformed time-dependently about 2 month after the tunnel excavation. The core samples around the deformed zones are characterized secondary mineral assemblages of smectite, cristobalite, tridymite, sulfides (pyrite and marcasite) and partially or completely reacted carbonates (calcite and siderite), which were formed by hydrothermal alteration under neutral to acidic condition below about 100 °C. The core samples also showed localized deterioration, such as crack formation and expansion, which occurred from few days to months after the drilling. The deterioration could be explained as a result of the cyclic physical and chemical weathering process with the oxidation of sulfide minerals, dissolution of carbonate mineral cementation and volumetric expantion of smectite. This weathering process is considered as a key factor for time-dependent tunnel deformation in the hydrothermally altered volcanic rocks. The zones of time-dependent deformation along a tunnel route can be predicted by the variations of whole-rock chemical compositions such as Na, Ca, Sr, Ba and S.
Spatial thermal radiometry contribution to the Massif Armoricain and the Massif Central France litho-structural study

NASA Technical Reports Server (NTRS)

Scanvic, J. Y. (Principal Investigator)

1980-01-01

Thermal zones delimited on HCMM images, by visual interpretation only, were correlated with geological units and carbonated rocks, granitic, and volcanic rocks were individualized rock signature is evolutive parameter and some distinctions were made by addition of day, night and seasonal thermal image interpretation. This analysis also demonstrated that forest cover does not mask the underlying rocks thermal signature. Thermal linears are associated with known tectonics but the observed thermal variations from day to night and from one to another represent a promising concept to be studied in function of neotectonics and hydrogeology. The thermal anomalies discovered represent a potential interest which is to be evaluated. Significant results were obtained in the Mont Dore area and additional geological targets were defined in the Paris Basin and the Montmarault granite.
Shale Fracture Analysis using the Combined Finite-Discrete Element Method

NASA Astrophysics Data System (ADS)

Carey, J. W.; Lei, Z.; Rougier, E.; Knight, E. E.; Viswanathan, H.

2014-12-01

Hydraulic fracturing (hydrofrac) is a successful method used to extract oil and gas from highly carbonate rocks like shale. However, challenges exist for industry experts estimate that for a single $10 million dollar lateral wellbore fracking operation, only 10% of the hydrocarbons contained in the rock are extracted. To better understand how to improve hydrofrac recovery efficiencies and to lower its costs, LANL recently funded the Laboratory Directed Research and Development (LDRD) project: "Discovery Science of Hydraulic Fracturing: Innovative Working Fluids and Their Interactions with Rocks, Fractures, and Hydrocarbons". Under the support of this project, the LDRD modeling team is working with the experimental team to understand fracture initiation and propagation in shale rocks. LANL's hybrid hydro-mechanical (HM) tool, the Hybrid Optimization Software Suite (HOSS), is being used to simulate the complex fracture and fragment processes under a variety of different boundary conditions. HOSS is based on the combined finite-discrete element method (FDEM) and has been proven to be a superior computational tool for multi-fracturing problems. In this work, the comparison of HOSS simulation results to triaxial core flooding experiments will be presented.
Mountain glaciation drives rapid oxidation of rock-bound organic carbon

PubMed Central

Horan, Kate; Hilton, Robert G.; Selby, David; Ottley, Chris J.; Gröcke, Darren R.; Hicks, Murray; Burton, Kevin W.

2017-01-01

Over millions of years, the oxidation of organic carbon contained within sedimentary rocks is one of the main sources of carbon dioxide to the atmosphere, yet the controls on this emission remain poorly constrained. We use rhenium to track the oxidation of rock-bound organic carbon in the mountain watersheds of New Zealand, where high rates of physical erosion expose rocks to chemical weathering. Oxidative weathering fluxes are two to three times higher in watersheds dominated by valley glaciers and exposed to frost shattering processes, compared to those with less glacial cover; a feature that we also observe in mountain watersheds globally. Consequently, we show that mountain glaciation can result in an atmospheric carbon dioxide source during weathering and erosion, as fresh minerals are exposed for weathering in an environment with high oxygen availability. This provides a counter mechanism against global cooling over geological time scales. PMID:28983510

Fracture Dissolution of Carbonate Rock: An Innovative Process for Gas Storage

DOE Office of Scientific and Technical Information (OSTI.GOV)

James W. Castle; Ronald W. Falta; David Bruce

2006-10-31

The goal of the project is to develop and assess the feasibility and economic viability of an innovative concept that may lead to commercialization of new gas-storage capacity near major markets. The investigation involves a new approach to developing underground gas storage in carbonate rock, which is present near major markets in many areas of the United States. Because of the lack of conventional gas storage and the projected growth in demand for storage capacity, many of these areas are likely to experience shortfalls in gas deliverability. Since depleted gas reservoirs and salt formations are nearly non-existent in many areas,more » alternatives to conventional methods of gas storage are required. The need for improved methods of gas storage, particularly for ways to meet peak demand, is increasing. Gas-market conditions are driving the need for higher deliverability and more flexibility in injection/withdrawal cycling. In order to meet these needs, the project involves an innovative approach to developing underground storage capacity by creating caverns in carbonate rock formations by acid dissolution. The basic concept of the acid-dissolution method is to drill to depth, fracture the carbonate rock layer as needed, and then create a cavern using an aqueous acid to dissolve the carbonate rock. Assessing feasibility of the acid-dissolution method included a regional geologic investigation. Data were compiled and analyzed from carbonate formations in six states: Indiana, Ohio, Kentucky, West Virginia, Pennsylvania, and New York. To analyze the requirements for creating storage volume, the following aspects of the dissolution process were examined: weight and volume of rock to be dissolved; gas storage pressure, temperature, and volume at depth; rock solubility; and acid costs. Hydrochloric acid was determined to be the best acid to use because of low cost, high acid solubility, fast reaction rates with carbonate rock, and highly soluble products (calcium chloride) that allow for the easy removal of calcium waste from the well. Physical and chemical analysis of core samples taken from prospective geologic formations for the acid dissolution process confirmed that many of the limestone samples readily dissolved in concentrated hydrochloric acid. Further, some samples contained oily residues that may help to seal the walls of the final cavern structure. These results suggest that there exist carbonate rock formations well suited for the dissolution technology and that the presence of inert impurities had no noticeable effect on the dissolution rate for the carbonate rock. A sensitivity analysis was performed for characteristics of hydraulic fractures induced in carbonate formations to enhance the dissolution process. Multiple fracture simulations were conducted using modeling software that has a fully 3-D fracture geometry package. The simulations, which predict the distribution of fracture geometry and fracture conductivity, show that the stress difference between adjacent beds is the physical property of the formations that has the greatest influence on fracture characteristics by restricting vertical growth. The results indicate that by modifying the fracturing fluid, proppant type, or pumping rate, a fracture can be created with characteristics within a predictable range, which contributes to predicting the geometry of storage caverns created by acid dissolution of carbonate formations. A series of three-dimensional simulations of cavern formation were used to investigate three different configurations of the acid-dissolution process: (a) injection into an open borehole with production from that same borehole and no fracture; (b) injection into an open borehole with production from that same borehole, with an open fracture; and (c) injection into an open borehole connected by a fracture to an adjacent borehole from which the fluids are produced. The two-well configuration maximizes the overall mass transfer from the rock to the fluid, but it results in a complex cavern shape. Numerical simulations were performed to evaluate the ability of storage caverns produced by the acid-dissolution method to store natural gas. In addition, analyses were conducted to evaluate cavern stability during gas injection and withdrawal from storage caverns created in carbonate formations by the acid-dissolution method. The stability analyses were conducted using FLAC2D, a commercially available geotechnical analysis and design software. The analyses indicate that a tall cylindrical cavern with a domed roof and floor will be stable under the expected range of in situ and operational conditions. This result suggests that it should be feasible to avoid mechanical instabilities that could potentially diminish the effectiveness of the storage facility. The feasibility of using pressure transients measured at the ground surface was investigated as a means to evaluate (Abstract truncated)« less
Authigenic carbon entombed in methane-soaked sediments from the northeastern transform margin of the Guaymas Basin, Gulf of California

NASA Astrophysics Data System (ADS)

Paull, Charles K.; Ussler, William; Peltzer, Edward T.; Brewer, Peter G.; Keaten, Rendy; Mitts, Patrick J.; Nealon, Jeffrey W.; Greinert, Jens; Herguera, Juan-Carlos; Elena Perez, M.

2007-06-01

Extensive ROV-based sampling and exploration of the seafloor was conducted along an eroded transform-parallel fault scarp on the northeastern side of the Guaymas Basin in the Gulf of California to observe the nature of fluids venting from the seafloor, measure the record left by methane-venting on the carbonates from this area, and determine the association with gas hydrate. One gas vent vigorous enough to generate a water-column gas plume traceable for over 800 m above the seafloor was found to emanate from a ˜10-cm-wide orifice on the eroded scarp face. Sediment temperature measurements and topography on a sub-bottom reflector recorded in a transform-parallel seismic reflection profile identified a subsurface thermal anomaly beneath the gas vent. Active chemosynthetic biological communities (CBCs) and extensive authigenic carbonates that coalesce into distinct chemoherm structures were encountered elsewhere along the eroded transform-parallel scarp. The carbon isotopic composition of methane bubbles flowing vigorously from the gas vent (-53.6±0.8‰ PDB) is comparable to methane found in sediment cores taken within the CBCs distributed along the scarp (-51.9±8.1‰ PDB). However, the δ13C value of the CO 2 in the vent gas (+12.4±1.1‰ PDB) is very distinct from those for dissolved inorganic carbon (DIC) (-35.8‰ to -2.9‰ PDB) found elsewhere along the scarp, including underneath CBCs. The δ13C values of the carbonate-rich sediments and rocks exposed on the seafloor today also span an unusually large range (-40.9‰ to +12.9‰ PDB) and suggest two distinct populations of authigenic carbonate materials were sampled. Unconsolidated sediments and some carbonate rocks, which have lithologic evidence for near-seafloor formation, have negative δ13C values, while carbonate rocks that clearly formed in the subsurface have positive δ13C values (up to +23.0‰) close to that measured for CO 2 in the vent gas. There appears to be two carbon sources for the authigenic carbonates: (1) deeply-sourced, isotopically heavy CO 2 (˜+12‰); and (2) isotopically light DIC derived from local anaerobic oxidation of methane at the sulfate-methane interface in the shallow subsurface. Addition of isotopically light methane-derived carbon at the seafloor may completely mask the isotopically heavy CO 2 signature (+12.4‰) in the underlying sediments. Thus, the authigenic carbonates may have formed from the same methane- and carbon dioxide-bearing fluid, but under different migration and alteration conditions, depending on how it migrated through the sediment column.
Space-time evolution of cataclasis in carbonate fault zones

NASA Astrophysics Data System (ADS)

Ferraro, Francesco; Grieco, Donato Stefano; Agosta, Fabrizio; Prosser, Giacomo

2018-05-01

The present contribution focuses on the micro-mechanisms associated to cataclasis of both calcite- and dolomite-rich fault rocks. This work combines field and laboratory data of carbonate fault cores currently exposed in central and southern Italy. By first deciphering the main fault rock textures, their spatial distribution, crosscutting relationships and multi-scale dimensional properties, the relative timing of Intragranular Extensional Fracturing (IEF), chipping, and localized shear is inferred. IEF was predominant within already fractured carbonates, forming coarse and angular rock fragments, and likely lasted for a longer period within the dolomitic fault rocks. Chipping occurred in both lithologies, and was activated by grain rolling forming minute, sub-rounded survivor grains embedded in a powder-like carbonate matrix. The largest fault zones, which crosscut either limestones or dolostones, were subjected to localized shear and, eventually, to flash temperature increase which caused thermal decomposition of calcite within narrow (cm-thick) slip zones. Results are organized in a synoptic panel including the main dimensional properties of survivor grains. Finally, a conceptual model of the time-dependent evolution of cataclastic deformation in carbonate rocks is proposed.
Publications - GMC 99 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 99 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Reference Unknown, 1988, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance data of ditch Report Report Information gmc099.pdf (383.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic
Publications - GMC 20 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

, rock-eval/pyrolysis, total organic carbon) and core logs for the David River USA #1-A, Hoodoo Lake Unit , 1969, Geochemical analysis (vitrinite reflectance, visual kerogen, rock-eval/pyrolysis, total organic gmc020.pdf (3.2 M) Keywords Kerogen; Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon; Vitrinite
Publications - GMC 72 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 72 Publication Details Title: Organic carbon, rock-eval pyrolysis, kerogen type, maturation , and vitrinite reflectance geochemical data, and a source rock evaluation for the Exxon OCS-Y-0280-1 publication sales page for more information. Bibliographic Reference Texaco, Inc., 1987, Organic carbon, rock
Publications - GMC 123 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 123 Publication Details Title: Total organic carbon and rock-eval pyrolysis data of select organic carbon and rock-eval pyrolysis data of select cuttings from the Chevron USA Akulik #1 well: Alaska Pyrolysis; Rock-Eval Pyrolysis Top of Page Department of Natural Resources, Division of Geological &
Hydrogeology of, and Simulation of Ground-Water Flow In, the Pohatcong Valley, Warren County, New Jersey

USGS Publications Warehouse

Carleton, Glen B.; Gordon, Alison D.

2007-01-01

A numerical ground-water-flow model was constructed to simulate ground-water flow in the Pohatcong Valley, including the area within the U.S. Environmental Protection Agency Pohatcong Valley Ground Water Contamination Site. The area is underlain by glacial till, alluvial sediments, and weathered and competent carbonate bedrock. The northwestern and southeastern valley boundaries are regional-scale thrust faults and ridges underlain by crystalline rocks. The unconsolidated sediments and weathered bedrock form a minor surficial aquifer and the carbonate rocks form a highly transmissive fractured-rock aquifer. Ground-water flow in the carbonate rocks is primarily downvalley towards the Delaware River, but the water discharges through the surficial aquifer to Pohatcong Creek under typical conditions. The hydraulic characteristics of the carbonate-rock aquifer are highly heterogeneous. Horizontal hydraulic conductivities span nearly five orders of magnitude, from 0.5 feet per day (ft/d) to 1,800 ft/d. The maximum transmissivity calculated is 37,000 feet squared per day. The horizontal hydraulic conductivities calculated from aquifer tests using public supply wells open to the Leithsville Formation and Allentown Dolomite are 34 ft/d (effective hydraulic conductivity) and 85 to 190 ft/d (minimum and maximum hydraulic conductivity, respectively, yielding a horizontal anisotropy ratio of 0.46). Stream base-flow data were used to estimate the net gain (or loss) for selected reaches on Brass Castle Creek, Shabbecong Creek, three smaller tributaries to Pohatcong Creek, and for five reaches on Pohatcong Creek. Estimated mean annual base flows for Brass Castle Creek, Pohatcong Creek at New Village, and Pohatcong Creek at Carpentersville (from correlations of partial- and continuous-record stations) are 2.4, 25, and 45 cubic feet per second (ft3/s) (10, 10, and 11 inches per year (in/yr)), respectively. Ground-water ages estimated using sulfur hexafluoride (SF6), chlorofluorocarbon (CFC), and tritium-helium age-dating techniques range from 0 to 27 years, with a median age of 6 years. Land-surface and ground-water water budgets were calculated, yielding an estimated rate of direct recharge tothe surficial aquifer of about 23 in/yr, and an estimated net recharge to the ground-water system within the area underlain by carbonate rock (11.4 mi2) of 29 in/yr (10 in/yr over the entire 33.3 mi2 basin). A finite-difference, numerical model was developed to simulate ground-water flow in the Pohatcong Valley. The four-layer model encompasses the entire carbonate-rock part of the valley. The carbonate-rock aquifer was modeled as horizontally anisotropic, with the direction of maximum transmissivity aligned with the longitudinal axis of the valley. All lateral boundaries are no-flow boundaries. Recharge was applied uniformly to the topmost active layer with additional recharge added near the lateral boundaries to represent infiltration of runoff from adjacent crystalline-rock areas. The model was calibrated to June 2001 water levels in wells completed in the carbonate-rock aquifer, August 2000 stream base-flow measurements, and the approximate ground-water age. The ground-water-flow model was constructed in part to test possible site contamination remediation alternatives. Four previously determined ground-water remediation alternatives (GW1, GW2, GW3, and GW4) were simulated. For GW1, the no-action alternative, simulated pathlines originating in the tetrachloroethene (PCE) and trichloroethene (TCE) source areas within the Ground-Water Contamination Site end at Pohatcong Creek near the confluence with Shabbecong Creek, although some particles went deeper in the aquifer system and ultimately discharge to Pohatcong Creek about 10 miles downvalley in Pohatcong Township. Remediation alternatives GW2, GW3, and GW4 include ground-water withdrawal, treatment, and reinjection. The design for GW2 includes wells in the TCE and PCE source areas that wit
Influences of pH and CO2 on the formation of Metasilicate mineral water in Changbai Mountain, Northeast China

NASA Astrophysics Data System (ADS)

Yan, Baizhong; Xiao, Changlai; Liang, Xiujuan; Wu, Shili

2017-07-01

Mineral dissolution reactions actively participate in controlling the composition of mineral water. In this study, water soluble, acidic-alkaline and carbonated solution experiments were designed, and mineral reaction mechanisms were researched using chemical kinetics and the minimum free-energy method. The results showed that the release of metasilicate was controlled by pH, CO2, and rock characteristics. In the water soluble experiment, the release process of metasilicate in powdered rocks reached equilibrium after 40 days, while metasilicate in solid rocks took 170 days. The release process of metasilicate in solid rocks satisfied an asymptotic model, while in powdered rocks it accorded with the Stanford reaction kinetic model. In the acidic-alkaline experiment, metasilicate was released earlier under acidic conditions (2.46 < pH < 7) than under alkaline conditions (7 < pH < 10.61). The release process of metasilicate under acidic conditions reached equilibrium in 40 days, compared with 60 days for alkaline conditions. The addition of CO2 to the water solution was beneficial to the formation of metasilicate. Under neutral pH conditions, the reaction barely occurred. Under alkaline conditions, metasilicate was produced by the hydrolysis of metasilicate minerals. Under acidic and additional CO2 conditions, metasilicate formation was mainly via the reaction of H+, CO2, and metasilicate minerals. From these results, we concluded that the metasilicate mineral water from the Changbai Mountains, Jingyu County, is generated by a combination of the hydrolysis of metasilicate minerals and the reaction of H+, CO2, and metasilicate minerals. These results can contribute to a better development and protection of the mineral water resources in the Changbai Mountains.
Carbonate rocks of the Seward Peninsula, Alaska: Their correlation and paleogeographic significance

USGS Publications Warehouse

Dumoulin, Julie A.; Harris, Alta; Repetski, John E.

2014-01-01

Paleozoic carbonate strata deposited in shallow platform to off-platform settings occur across the Seward Peninsula and range from unmetamorphosed Ordovician–Devonian(?) rocks of the York succession in the west to highly deformed and metamorphosed Cambrian–Devonian units of the Nome Complex in the east. Faunal and lithologic correlations indicate that early Paleozoic strata in the two areas formed as part of a single carbonate platform. The York succession makes up part of the York terrane and consists of Ordovician, lesser Silurian, and limited, possibly Devonian rocks. Shallow-water facies predominate, but subordinate graptolitic shale and calcareous turbidites accumulated in deeper water, intraplatform basin environments, chiefly during the Middle Ordovician. Lower Ordovician strata are mainly lime mudstone and peloid-intraclast grainstone deposited in a deepening upward regime; noncarbonate detritus is abundant in lower parts of the section. Upper Ordovician and Silurian rocks include carbonate mudstone, skeletal wackestone, and coral-stromatoporoid biostromes that are commonly dolomitic and accumulated in warm, shallow to very shallow settings with locally restricted circulation. The rest of the York terrane is mainly Ordovician and older, variously deformed and metamorphosed carbonate and siliciclastic rocks intruded by early Cambrian (and younger?) metagabbros. Older (Neoproterozoic–Cambrian) parts of these units are chiefly turbidites and may have been basement for the carbonate platform facies of the York succession; younger, shallow- and deep-water strata likely represent previously unrecognized parts of the York succession and its offshore equivalents. Intensely deformed and altered Mississippian carbonate strata crop out in a small area at the western edge of the terrane. Metacarbonate rocks form all or part of several units within the blueschist- and greenschist-facies Nome Complex. The Layered sequence includes mafic meta¬igneous rocks and associated calcareous metaturbidites of Ordovician age as well as shallow-water Silurian dolostones. Scattered metacarbonate rocks are chiefly Cambrian, Ordovician, Silurian, and Devonian dolostones that formed in shallow, warm-water settings with locally restricted circulation and marbles of less constrained Paleozoic age. Carbonate metaturbidites occur on the northeast and southeast coasts and yield mainly Silurian and lesser Ordovician and Devonian conodonts; the northern succession also includes debris flows with meter-scale clasts and an argillite interval with Late Ordovician graptolites and lenses of radiolarian chert. Mafic igneous rocks at least partly of Early Devonian age are common in the southern succession. Carbonate rocks on Seward Peninsula experienced a range of deformational and thermal histories equivalent to those documented in the Brooks Range. Conodont color alteration indices (CAIs) from Seward Peninsula, like those from the Brooks Range, define distinct thermal provinces that likely reflect structural burial. Penetratively deformed high-pressure metamorphic rocks of the Nome Complex (CAIs ≥5) correspond to rocks of the Schist belt in the southern Brooks Range; both record subduction during early stages of the Jurassic–Cretaceous Brooks Range orogeny. Weakly metamorphosed to unmetamorphosed strata of the York terrane (CAIs mainly 2–5), like Brooks Range rocks in the Central belt and structural allochthons to the north, experienced moderate to shallow burial during the main phase of the Brooks Range orogeny. The nature of the contact between the York terrane and the Nome Complex is uncertain; it may be a thrust fault, an extensional surface, or a thrust fault later reactivated as an extensional fault. Lithofacies and biofacies data indicate that, in spite of their divergent Mesozoic histories, rocks of the York terrane and protoliths of the Nome Complex formed as part of the same lower Paleozoic carbonate platform. Stratigraphies in both
Hydrogeology of the carbonate rocks of the Lebanon Valley, Pennsylvania

USGS Publications Warehouse

Meisler, Harold

1963-01-01

The Lebanon Valley, which is part of the Great Valley in southeastern Pennsylvania, is underlain by carbonate rocks in the southern part and by shale in the northern part. The carbonate rocks consist of alternating beds of limestone and dolomite of Cambrian and Ordovician age. Although the beds generally dip to the south, progressively younger beds crop out to the north, because the rocks are overturned. The stratigraphic units, from oldest to youngest, are: the Buffalo Springs Formation, Snitz Creek, Schaefferstown, Millbach, and Richland Formations of the Conococheague Group; the Stonehenge, Rickenbach, Epler, and Ontelaunee Formations of the Beekmantown Group; and the Annville, Myerstown, and Hershey Limestones.
Geology and hydrogeology of the Caribbean islands aquifer system of the Commonwealth of Puerto Rico and the U.S. Virgin Islands

USGS Publications Warehouse

Renken, Robert A.; Ward, W. C.; Gill, I.P.; Gómez-Gómez, Fernando; Rodríguez-Martínez, Jesús; ,

2002-01-01

Poorly lithified to unconsolidated carbonate and clastic sedimentary rocks of Tertiary (Oligocene to Pliocene) and Quaternary (Pleistocene to Holocene) age compose the South Coast aquifer and the North Coast limestone aquifer system of Puerto Rico; poorly lithified to unlithified carbonate rocks of late Tertiary (early Miocene to Pliocene) age make up the Kingshill aquifer of St. Croix, U.S. Virgin Islands. The South Coast aquifer, North Coast limestone aquifer system, and Kingshill aquifer are the most areally extensive and function as the major sources of ground water in the U.S. Caribbean Islands Regional Aquifer-System Analysis (CI-RASA) study area. In Puerto Rico's South Coast ground-water province, more than 1,000 meters of clastic and carbonate rocks of Oligocene to Pliocene age infill the South Coast Tertiary Basin. The pattern of lithofacies within this basin appears to have been controlled by changes in base level that were, at times, dominated by tectonic movement (uplift and subsidence), but were also influenced by eustasy. Deposition of the 70-kilometer long and 3- to 8-kilometer wide fan-delta plain that covers much of the South Coast ground-water province occurred largely in response to glacially-induced changes in sea level and climate during the Quaternary period. Tectonic movement played a much less important role during the Quaternary. The North Coast ground-water province of Puerto Rico is underlain by homoclinal coastal plain wedge of carbonate and siliciclastic rocks that infill the North Coast Tertiary Basin and thicken to more than 1,700 meters. A thin basal siliciclastic sequence of late Oligocene age is overlain by a thick section of mostly carbonate rocks of Oligocene to middle Miocene age. Globigerinid limestone of late Miocene to Pliocene age crops out and lies in the shallow subsurface areas of northwestern Puerto Rico. Oligocene to middle Miocene age rocks tentatively can be divided into five depositional sequences and associated systems tracts; these rocks record carbonate and minor siliciclastic deposition that occurred in response to changes in relative sea level. The Cibao Formation represents the most complex of these sequences and contains a varied facies of carbonate, mixed carbonate-siliciclastic, and siliciclastic rocks that reflect differential uplift, subsidence, and transgression of the sea. Uplift, graben formation, and gradual shallowing of the sea are reflected within the bathyal-dominated sedimentary facies of the Kingshill Limestone in St. Croix, U.S. Virgin Islands. Reef-tract limestone beds of Pliocene age were subject to exposure, resubmergence, and meteoric leaching of aragonitic skeletal debris; these beds contain patchy lenses of dolomite that are restricted to a small, structurally-controlled embayment. The South Coast aquifer, the principal water-bearing unit of Puerto Rico's South Coast ground-water province, consists of boulder- to silt-size detritus formed by large and small coalescing fan deltas of Pleistocene to Holocene age. Deep well data indicates that it is possible to vertically separate and group a highly complex and irregular-bedded detrital sequence that underlies distal parts of the fan-delta plain into discrete water-bearing units if correlated with 30- to 40-meter thick, eustatically-controlled depositional cycles. Lithofacies maps show that greatest hydraulic conductivity within the fan-delta plain is generally associated with proximal fan and midfan areas. Distal and interfan areas are least permeable. Alluvial valley aquifers located in the western part of the South Coast ground-water province are important local sources of water supply and appear to contain some of the same physical and hydraulic characteristics as the South Coast aquifer. Older sedimentary rocks within the basin are poor aquifers; conglomeratic beds are well-cemented, and carbonate beds do not contain well-developed solution features, except locally where the beds are over
Earth's early fossil record: Why not look for similar fossils on Mars?

NASA Technical Reports Server (NTRS)

Awramik, Stanley M.

1989-01-01

The oldest evidence of life on Earth is discussed with attention being given to the structure and formation of stromatolites and microfossils. Fossilization of microbes in calcium carbonate or chert media is discussed. In searching for fossil remains on Mars, some lessons learned from the study of Earth's earliest fossil record can be applied. Certain sedimentary rock types and sedimentary rock configurations should be targeted for investigation and returned by the Martian rover and ultimately by human explorers. Domical, columnar to wavy laminated stratiform sedimentary rocks that resemble stromatolites should be actively sought. Limestone, other carbonates, and chert are the favored lithology. Being macroscopic, stromatolites might be recognized by an intelligent unmanned rover. In addition, black, waxy chert with conchoidal fracture should be sought. Chert is by far the preferred lithology for the preservation of microbes and chemical fossils. Even under optimal geological conditions (little or no metamorphism or tectonic alteration, excellent outcrops, and good black chert) and using experienced field biogeologists, the chances of finding well preserved microbial remains in chert are very low.
Analysis of Shublik Formation rocks from Mt. Michelson quadrangle, Alaska

USGS Publications Warehouse

Detterman, Robert L.

1970-01-01

Analysis of 88 samples from the Shublik formation on Fire Creek, Mt. Michelson Quadrangle, Alaska, are presented in tabular form. The results include the determination of elements by semiquantitative spectrographic analysis, phosphate by X-ray fluorescence, carbon dioxide by acid decomposable carbonate, total carbon by induction furnace, carbonate carbon by conversion using the conversion factor of 0.2727 for amount of carbon in carbon dioxide, and organic carbon by difference. A seven- cycle semilogarithmic chart presents the data graphically and illustrates the range, mode, and mean for some of the elements. The chart shows, also, the approximate concentration of the same elements in rocks similar to the black shale and limestone of the Shublik Formation. Each sample represents 5 feet of section and is composed of rock chips taken at 1 - foot intervals. The samples are keyed into a stratigraphic column of the formation. Rocks of the Shublik Formation contain anomalously high concentrations of some of the elements. These same elements might be expected to be high in some of the petroleum from northern Alaska if the Shublik Formation is a source for this petroleum. Several of the stratigraphic intervals may represent, also, a low-grade phosphate deposit.
The presence of carbonates on Mars: origin, terrestrial analogues and analytical tecniques ambiguity

NASA Astrophysics Data System (ADS)

Marinangeli, Lucia; Liberi, Francesca; Pompilio, Loredana; Piluso, Eugenio; Rosatelli, Gianluigi; Tranquilli, Andrea; Pepe, Monica

2013-04-01

The most common cause of carbonates formation on Earth is the chemical deposition from Ca-rich waters in sedimentary basins, mostly in shallow water. The lack of widespread exposure of carbonates on the Mars' surface in areas where geomorphological and sedimentological mapping confirms the presence of water for a long period of the Martian history, led us to look for a potential different origin of the carbonates identified on CRISM data [1, 2,3]. We suggest the presence of carbonatites on Mars and we have also investigated the capabilities of analytical tecniques for mineralogical analysis to recognise these peculiar type of rocks. Carbonatites are igneous rocks containing more than 50 percent of carbonate minerals and associated silicate minerals as olivine, pyroxene and phyllosilicates. Carbonatites are associated with alkali silicate rocks that are usually of nephelinitic or melilititic affinity. The Martian carbonates are often present in layered rocks and in association with hydrated Fe-Mg silicates (clays family) and kaolinite-group minerals at places [1]. This mineralogical association is very similar to an water-altered carbonatite. We have compared the compositional and mineralogical affinity of some carbonatite samples from different alkaline-carbonatite complexes from Uganda, Spain and Italy, with the mineralogy described for the carbonate- and phyllosolicate rich rocks on Mars, using the XRD and IR analyses. The mineral assemblage has been defined through petrographic analyses as well. It is important to stress that only with XRD analysis some minerals diagnos-tic of carbonatitic assemblage (i.e. melilite) were identified. The relationships between carbonatites and their associated silicate rocks are complex and are still not fully understood on Earth as well, however, it deserves further investigations to better explain the carbonates and silicate volcanic rocks on Mars and its crustal dynamics. References: [1] Michalski and Niles, 2010, Nature Geoscience, 751-755. [2] Helmann et al., 2008, Science, 322, 1828-1832. [3] Morris et al., 2010, Science, 329, 421-424.
Families of miocene monterey crude oil, seep, and tarball samples, coastal California

USGS Publications Warehouse

Peters, K.E.; Hostettler, F.D.; Lorenson, T.D.; Rosenbauer, R.J.

2008-01-01

Biomarker and stable carbon isotope ratios were used to infer the age, lithology, organic matter input, and depositional environment of the source rocks for 388 samples of produced crude oil, seep oil, and tarballs to better assess their origins and distributions in coastal California. These samples were used to construct a chemometric (multivariate statistical) decision tree to classify 288 additional samples. The results identify three tribes of 13C-rich oil samples inferred to originate from thermally mature equivalents of the clayey-siliceous, carbonaceous marl and lower calcareous-siliceous members of the Monterey Formation at Naples Beach near Santa Barbara. An attempt to correlate these families to rock extracts from these members in the nearby COST (continental offshore stratigraphic test) (OCS-Cal 78-164) well failed, at least in part because the rocks are thermally immature. Geochemical similarities among the oil tribes and their widespread distribution support the prograding margin model or the banktop-slope-basin model instead of the ridge-and-basin model for the deposition of the Monterey Formation. Tribe 1 contains four oil families having geochemical traits of clay-rich marine shale source rock deposited under suboxic conditions with substantial higher plant input. Tribe 2 contains four oil families with traits intermediate between tribes 1 and 3, except for abundant 28,30-bisnorhopane, indicating suboxic to anoxic marine marl source rock with hemipelagic input. Tribe 3 contains five oil families with traits of distal marine carbonate source rock deposited under anoxic conditions with pelagic but little or no higher plant input. Tribes 1 and 2 occur mainly south of Point Conception in paleogeographic settings where deep burial of the Monterey source rock favored petroleum generation from all three members or their equivalents. In this area, oil from the clayey-siliceous and carbonaceous marl members (tribes 1 and 2) may overwhelm that from the lower calcareous-siliceous member (tribe 3) because the latter is thinner and less oil-prone than the overlying members. Tribe 3 occurs mainly north of Point Conception where shallow burial caused preferential generation from the underlying lower calcareous-siliceous member or another unit with similar characteristics. In a test of the decision tree, 10 tarball samples collected from beaches in Monterey and San Mateo counties in early 2007 were found to originate from natural seeps representing different organofacies of Monterey Formation source rock instead from one anthropogenic pollution event. The seeps apparently became more active because of increased storm activity. Copyright ?? 2008. The American Association of Petroleum Geologists. All rights reserved.
Publications - GMC 26 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 26 Publication Details Title: Geochemical data (total organic carbon, rock-eval pyrolysis, and Reference Unknown, 1984, Geochemical data (total organic carbon, rock-eval pyrolysis, and vitrinite ; Total Organic Carbon; Vitrinite Reflectance Top of Page Department of Natural Resources, Division of
Publications - GMC 29 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 29 Publication Details Title: Geochemical analysis (total organic carbon, rock-eval pyrolysis Reference Minder, Michael, and Shell Oil Company, 1985, Geochemical analysis (total organic carbon, rock ; Total Organic Carbon; Vitrinite Reflectance Top of Page Department of Natural Resources, Division of
Publications - GMC 334 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 334 Publication Details Title: Total Organic Carbon and Rock Eval with additional geochemical ConocoPhillips, and Baseline Resolution Inc. Analytical Laboratories, 2006, Total Organic Carbon and Rock Eval ) Keywords Total Organic Carbon Top of Page Department of Natural Resources, Division of Geological &
Publications - GMC 56 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 56 Publication Details Title: Total organic carbon, extractable organic matter, rock-eval publication sales page for more information. Bibliographic Reference Mobil Oil Coporation, 1986, Total organic carbon, extractable organic matter, rock-eval parameters, isoprenoid ratios, carbon preference index, and

Publications - GMC 25 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 25 Publication Details Title: Geochemical analysis (total organic carbon, rock-eval pyrolysis Reference Unknown, 1984, Geochemical analysis (total organic carbon, rock-eval pyrolysis, kerogen type ; Total Organic Carbon; Vitrinite Reflectance Top of Page Department of Natural Resources, Division of
Publications - GMC 125 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 125 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Reference Cunningham, K., and Shell Oil Company, 1989, Total organic carbon, rock-eval pyrolysis, and Pyrolysis; Total Organic Carbon; Vitrinite Reflectance Top of Page Department of Natural Resources, Division
Publications - GMC 28 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 28 Publication Details Title: Geochemical analysis (total organic carbon, rock-eval pyrolysis Reference Brown and Ruth Laboratories, Inc., 1985, Geochemical analysis (total organic carbon, rock-eval Organic Carbon Top of Page Department of Natural Resources, Division of Geological & Geophysical
Publications - GMC 126 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 126 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Reference Unknown, 1989, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance data of Organic Carbon; Vitrinite Reflectance Top of Page Department of Natural Resources, Division of Geological
Publications - GMC 143 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 143 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Reference Unknown, 1989, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance data of Organic Carbon; Vitrinite Reflectance Top of Page Department of Natural Resources, Division of Geological
Publications - GMC 122 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 122 Publication Details Title: Total organic carbon, rock-eval pyrolysis, vitrinite for more information. Bibliographic Reference Exxon, and Geo-Strat, Inc., 1989, Total organic carbon Information gmc122.pdf (1.4 M) Keywords Kerogen; Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon
Publications - GMC 207 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 207 Publication Details Title: Total organic carbon, rock-eval, and vitrinite reflectance data for more information. Bibliographic Reference Unknown, 1993, Total organic carbon, rock-eval, and Report Information gmc207.pdf (165.0 K) Keywords Total Organic Carbon; Vitrinite Reflectance Top of Page
Publications - GMC 19 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 19 Publication Details Title: Geochemical analysis (total organic carbon-rock-eval, vitrinite information. Bibliographic Reference Unknown, [n.d.], Geochemical analysis (total organic carbon-rock-eval K) Keywords Total Organic Carbon; Vitrinite Reflectance Top of Page Department of Natural Resources
Publications - GMC 62 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 62 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite . Bibliographic Reference Unknown, 1985, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance Pyrolysis; Total Organic Carbon; Vitrinite Reflectance Top of Page Department of Natural Resources, Division
Publications - GMC 66 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 66 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Reference Unknown, 1987, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance geochemical Organic Carbon; Vitrinite Reflectance Top of Page Department of Natural Resources, Division of Geological
Publications - GMC 142 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 142 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite Reference Unknown, 1989, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance data of Organic Carbon; Vitrinite Reflectance Top of Page Department of Natural Resources, Division of Geological
Publications - GMC 59 | Alaska Division of Geological & Geophysical Surveys

Science.gov Websites

DGGS GMC 59 Publication Details Title: Total organic carbon, rock-eval pyrolysis, and vitrinite . Bibliographic Reference Unknown, 1985, Total organic carbon, rock-eval pyrolysis, and vitrinite reflectance -Eval Pyrolysis; Total Organic Carbon; Vitrinite Reflectance Top of Page Department of Natural Resources
Dynamic Pore-Scale Imaging of Reactive Transport in Heterogeneous Carbonates at Reservior Conditions

NASA Astrophysics Data System (ADS)

Menke, Hannah; Bijeljic, Branko; Andrew, Matthew; Blunt, Martin

2014-05-01

Sequestering carbon in deep geologic formations is one way of reducing anthropogenic CO2 emissions. Carbon capture, Utilization, and Storage (CCUS) in carbonate reservoirs has the added benefit of mobilizing more oil for extraction, increasing oil reservoir yield, and generating revenue while also mitigating climate change. The magnitude, speed, and type of dissolution are dependent the intrinsic properties of the rock. Understanding how small changes in the pore structure affect dissolution is paramount for successful predictive modelling both on the pore-scale and for up-scaled reservoir simulations. We propose an experimental method whereby both 'Pink Beam' synchrotron radiation and a Micro-CT lab source are used in dynamic X-ray microtomography to investigate the pore structure changes in carbonate rocks of varying heterogeneity at high temperatures and pressures. Four carbonate rock types were studied, two relatively homogeneous carbonates, Ketton and Mt. Gambier, and two very heterogeneous carbonates, Estalliades and Portland Basebed. Each rock type was imaged under the same reservoir and flow conditions to gain insight into the impact of heterogeneity. A 4-mm carbonate core was injected with CO2-saturated brine at 10 MPa and 50oC for 2 hours. Depending on sample heterogeneity and X-ray source, tomographic images were taken at between 30-second and 20-minute time-resolutions and a 4-micron spatial resolution during injection. Changes in porosity, permeability, and structure were obtained by first binning and filtering the images, then binarizing them with watershed segmentation, and finally extracting a pore/throat network. Furthermore, pore-scale flow modelling was performed directly on the binarized image and used to track velocity distributions as the pore network evolved. Significant differences in dissolution type and magnitude were found for each rock type. The most homogeneous carbonate, Ketton, was seen to have predominately uniform dissolution with minor dissolution rate differences between the pores and pore throats. This was not true for the heterogeneous carbonates, Estalliades and Portland Basebed, which formed wormholes. Pore-scale modelling of flow directly on the voxels showed the differences in the evolution of complex flow fields with changes in dissolution regime. The PDFs of normalized velocity for uniform dissolution showed that the maximum pore velocity within the system decreased as dissolution occurred. This is due to dissolution enlarging pores and pore throats. However, in the wormholing regime, there was a large increase in maximum velocity once the wormhole broke through the length of the core and a preferential flow path was created. Additionally, this study serves as a unique benchmark for pore-scale reactive transport modelling directly on the binarized Micro-CT images. This dynamic pore-scale imaging method offers advantages in helping fully explain the dominant physical and chemical processes at the pore scale so that they may be up-scaled to the reservoir scale for increased accuracy in model prediction.
Publications - GMC 114 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 114 Publication Details Title: Total organic carbon and rock eval pyrolysis data and analysis and Ruth Laboratories, Inc., 1989, Total organic carbon and rock eval pyrolysis data and analysis for gmc114.pdf (171.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis Top of Page Department of Natural Resources
Publications - GMC 290 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 290 Publication Details Title: Organic carbon and rock-eval pyrolysis data of cuttings from Reference Unknown, 1999, Organic carbon and rock-eval pyrolysis data of cuttings from the Husky Oil NPR Products Report Report Information gmc290.pdf (177.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis Top of Page
Publications - GMC 130 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 130 Publication Details Title: Total organic carbon and rock-eval pyrolysis data of cuttings Reference Unknown, 1989, Total organic carbon and rock-eval pyrolysis data of cuttings and core from the Report Report Information gmc130.pdf (208.0 K) Keywords Pyrolysis; Rock-Eval Pyrolysis Top of Page
Mass transfer and fluid evolution in late-metamorphic veins, Rhenish Massif (Germany): insight from alteration geochemistry and fluid-mineral equilibria modeling

NASA Astrophysics Data System (ADS)

Marsala, Achille; Wagner, Thomas

2016-08-01

Element mobility and fluid-rock interaction related to the formation of late-metamorphic quartz veins have been studied by combination of mineral chemistry, whole-rock geochemistry, mass balance analysis and fluid-mineral equilibria modeling. The quartz veins are hosted by very low-grade metasedimentary rocks of the fold-and-thrust belt of the Rhenish Massif (Germany). The veins record two stages of evolution, a massive vein filling assemblage with elongate-blocky quartz, chlorite, apatite and albite, and a later open space filling assemblage with euhedral crystals of quartz, ankerite-dolomite and minor calcite and sulfides. Detailed mass balance analysis of an alteration profile adjacent to a representative quartz vein demonstrates that element mobility is restricted to the proximal zone. The most important element changes are gain of Ca, Fe, Mg, Mn, P and CO2, and loss of Si, K and Na. The data demonstrate that wall-rock carbonation is one of the main alteration features, whereas mobility of Si, K and Na are related to dissolution of quartz and destruction of detrital feldspar and muscovite. The whole-rock geochemical data, in conjunction with fluid composition data and pressure-temperature estimates, were used as input for fluid-mineral equilibria modeling in the system Si-Al-Fe-Mg-Ca-Na-K-C-S-O-H-B-F-Cl. Modeling involved calculation of rock-buffered fluid compositions over the temperature interval 100-500 °C, and reaction-path simulations where a rock-buffered high-temperature fluid reacts with fresh host-rocks at temperatures of 400, 300 and 200 °C. Calculated rock-buffered fluid compositions demonstrate that retrograde silica solubility is a strong driving force for quartz leaching in the temperature-pressure window of 380-450 °C and 0.5 kbar. These conditions overlap with the estimated temperatures for the initial stage of vein formation. Reaction-path models show that high-temperature alteration can produce the observed silica leaching, suggesting that fast advection of external hot fluids from deeper crustal levels was essential for the early stage of vein formation. Fluid advection must have occurred as multiple pulses, which allowed for periods of influx of fluids that leached quartz, alternating with periods of cooling and quartz precipitation in the veins. Reaction-path models at high temperatures (300-400 °C) do not produce carbonate alteration, whereas fluid-rock reaction at 200 °C produces carbonate alteration, consistent with the temperature estimates for the late-stage vein carbonate assemblage. Comparison between modeling results and geochemical data suggests that the observed alteration features are the product of fluid-rock reaction under conditions where the external fluid gradually cooled down and evolved with time. The results of this study highlight the importance of late-orogenic fluid migration for the formation of quartz vein arrays in fold-and-thrust belts.
Hydrogeology of, and simulation of ground-water flow in a mantled carbonate-rock system, Cumberland Valley, Pennsylvania

USGS Publications Warehouse

Chichester, D.C.

1996-01-01

The U.S. Geological Survey conducted a study in a highly productive and complex regolith-mantled carbonate valley in the northeastern part of the Cumberland Valley, Pa., as part of its Appalachian Valleys and Piedmont Regional Aquifer-system Analysis program. The study was designed to quantify the hydrogeologic characteristics and understand the ground-water flow system of a highly productive and complex thickly mantled carbonate valley. The Cumberland Valley is characterized by complexly folded and faulted carbonate bedrock in the valley bottom, by shale and graywacke to the north, and by red-sedimentary and diabase rocks in the east-southeast. Near the southern valley hillslope, the carbonate rock is overlain by wedge-shaped deposit of regolith, up to 450 feet thick, that is composed of residual material, alluvium, and colluvium. Locally, saturated regolith is greater than 200 feet thick. Seepage-run data indicate that stream reaches, near valley walls, are losing water from the stream, through the regolith, to the ground-water system. Results of hydrograph-separation analyses indicate that base flow in stream basins dominated by regolith-mantled carbonate rock, carbonate rock, and carbonate rock and shale are 81.6, 93.0, and 67.7 percent of total streamflow, respectively. The relative high percentage for the regolith-mantled carbonate-rock basin indicates that the regolith stores precipitation and slowly, steadily releases this water to the carbonate-rock aquifer and to streams as base flow. Anomalies in water-table gradients and configuration are a result of topography and differences in the character and distribution of overburden material, permeability, rock type, and geologic structure. Most ground-water flow is local, and ground water discharges to nearby springs and streams. Regional flow is northeastward to the Susquehanna River. Average-annual water budgets were calculated for the period of record from two continuous streamflow-gaging stations. Average-annual precipitation range from 39.0 to 40.5 inches, and averages about 40 inches for the model area. Average-annual recharge, which was assumed equal to the average-annual base flow, ranged from 12 inches for the Conodoguinet Creek, and 15 inches for the Yellow Breeches Creek. The thickly-mantled carbonate system was modeled as a three- dimensional water-table aquifer. Recharge to, ground-water flow through, and discharge from the Cumberland Valley were simulated. The model was calibrated for steady-state conditions using average recharge and discharge data. Aquifer horizontal hydraulic conductivity was calculated from specific-capacity data for each geologic unit in the area. Particle-tracking analyses indicate that interbasin and intrabasin flows of groundwater occur within the Yellow Breeches Creek Basin and between the Yellow Breeches and Conodoguinet Creek Basins.
Lithogeochemical character of the near-surface bedrock in the Connecticut, Housatonic, and Thames River Basins

USGS Publications Warehouse

Robinson, Gilpin R.; Peper, John D.; Steeves, Peter A.; Desimone, Leslie A.

1999-01-01

This data layer shows the generalized lithologic and geochemical (lithogeochemical) character of near-surface bedrock in the Connecticut, Housatonic, and Thames River Basins and several other small basins that drain into Long Island Sound from Connecticut. The area includes most of Connecticut, western Massachusetts, eastern Vermont, western New Hampshire, and small parts of Rhode Island, New York, and Quebec, Canada.Bedrock geologic rock units are classified into 29 lithogeochemical rock units, on the basis of the relative reactivity of their constituent minerals to dissolution and other weathering reactions and the presence of carbonate or sulfide minerals. The 29 lithogeochemical units (28 of which can be found in the study area) can be grouped into 6 major categories: (1) carbonate-rich rocks, (2) carbonate-poor, clastic sedimentary rocks restricted to distinct depositional basins, (3) metamorphosed, clastic sedimentary rocks (primarily noncalcareous), (4) mafic igneous rocks and their metamorphic equivalents, (5) ultramafic rocks, and (6) felsic igneous and plutonic rocks and their metamorphic equivalents. The lithogeochemical rock units also are grouped into nine lithologic and physiographic provinces (lithophysiographic domains), which can be further grouped into three major regions: (1) western highlands and lowlands, (2) central lowlands, and (3) eastern highlands.
Martian Cryogenic Carbonate Formation: Stable Isotope Variations Observed in Laboratory Studies

NASA Technical Reports Server (NTRS)

Socki, Richard A.; Niles, Paul B.; Sun, Tao; Fu, Qi; Romanek, Christopher S.; Gibson, Everett K. Jr.

2014-01-01

The history of water on Mars is tied to the formation of carbonates through atmospheric CO2 and its control of the climate history of the planet. Carbonate mineral formation under modern martian atmospheric conditions could be a critical factor in controlling the martian climate in a means similar to the rock weathering cycle on Earth. The combination of evidence for liquid water on the martian surface and cold surface conditions suggest fluid freezing could be very common on the surface of Mars. Cryogenic calcite forms easily from freezing solutions when carbon dioxide degasses quickly from Ca-bicarbonate-rich water, a process that has been observed in some terrestrial settings such as arctic permafrost cave deposits, lake beds of the Dry Valleys of Antarctica, and in aufeis (river icings) from rivers of N.E. Alaska. A series of laboratory experiments were conducted that simulated cryogenic carbonate formation on Mars in order to understand their isotopic systematics. The results indicate that carbonates grown under martian conditions show variable enrichments from starting bicarbonate fluids in both carbon and oxygen isotopes beyond equilibrium values.

Stratigraphy of the Hanna Basin, Wyoming

USGS Publications Warehouse

Bowen, C.F.

1918-01-01

Carbon County, Wyo., has attracted the attention of geologists since the days of the territorial surveys under King, Hayden, and Powell. During this earlier work all the rocks (except the North Park formation) over-lying the uppermost beds of marine origin were grouped in a single formation, for which the name Laramie was proposed.
An experimental study of the carbonation of serpentinite and partially serpentinised peridotites

NASA Astrophysics Data System (ADS)

Lacinska, Alicja M.; Styles, Michael T.; Bateman, Keith; Hall, Matthew; Brown, Paul D.

2017-06-01

In situ sequestration of CO2 in mantle peridotites has been proposed as a method to alleviate the amount of anthropogenic CO2 in the atmosphere. This study presents the results of eight-month long laboratory fluid-rock experiments on representative mantle rocks from the Oman-United Arab Emirates ophiolite to investigate this process. Small core samples (3 cm long) were reacted in wet supercritical CO2 and CO2-saturated brine at 100 bar and 70°C. The extent of carbonate formation, and hence the degree of carbon sequestration, varied greatly depending on rock type, with serpentinite (lizardite-dominated) exhibiting the highest capacity, manifested by the precipitation of magnesite MgCO3 and ferroan magnesite (Mg,Fe)CO3. The carbonate precipitation occurred predominantly on the surface of the core and subordinately within cross-cutting fractures. The extent of the CO2 reactions appeared to be principally controlled by the chemical and mineralogical composition of the rock, as well as the rock texture, with all these factors influencing the extent and rate of mineral dissolution and release of Mg and Fe for subsequent reaction with the CO2. It was calculated that ≈ 0.7 g of CO2 was captured by reacting ≈ 23 g of serpentinite, determined by the mass of magnesite formed. This equates to ≈ 30 kg CO2 per tonne of host rock, equivalent to ≈ 3% carbonation in half a year. However, recycling of carbonate present in veins within the original rock sample could mean that the overall amount is around 2%. The increased reactivity of serpentinite was associated with preferential dissolution of more reactive types of serpentine minerals and brucite, that were mainly present in the cross-cutting veins. The bulk of the serpentinite rock was little affected. This study, using relatively short term experiments, suggests that serpentinite might be a good host rock for CO2 sequestration, although long term experiments might prove that dunite and harzburgite could be an effective in an engineered system of CCSM. Wet scCO2 proved to be chemically aggressive than CO2-saturated brine and its ingress along fractures and grain boundaries resulted in greater host rock dissolution and subsequent carbonate precipitation.
Delineation of Magnesium-rich Ultramafic Rocks Available for Mineral Carbon Sequestration in the United States

USGS Publications Warehouse

Krevor, S.C.; Graves, C.R.; Van Gosen, B. S.; McCafferty, A.E.

2009-01-01

The 2005 Intergovernmental Panel on Climate Change report on Carbon Dioxide Capture and Storage suggested that a major gap in mineral carbon sequestration is locating the magnesium-silicate bedrock available to sequester CO2. It is generally known that silicate minerals with high concentrations of magnesium are suitable for mineral carbonation. However, no assessment has been made covering the entire United States detailing their geographical distribution and extent, or evaluating their potential for use in mineral carbonation. Researchers at Columbia University and the U.S. Geological Survey have developed a digital geologic database of ultramafic rocks in the continental United States. Data were compiled from varied-scale geologic maps of magnesium-silicate ultramafic rocks. These rock types are potentially suitable as source material for mineral carbon-dioxide sequestration. The focus of the national-scale map is entirely on suitable ultramafic rock types, which typically consist primarily of olivine and serpentine minerals. By combining the map with digital datasets that show non-mineable lands (such as urban areas and National Parks), estimates on potential depth of a surface mine, and the predicted reactivities of the mineral deposits, one can begin to estimate the capacity for CO2 mineral sequestration within the United States. ?? 2009 Elsevier Ltd. All rights reserved.
Modeling of carbonate reservoir variable secondary pore space based on CT images

NASA Astrophysics Data System (ADS)

Nie, X.; Nie, S.; Zhang, J.; Zhang, C.; Zhang, Z.

2017-12-01

Digital core technology has brought convenience to us, and X-ray CT scanning is one of the most common way to obtain 3D digital cores. However, it can only provide the original information of the only samples being scanned, and we can't modify the porosity of the scanned cores. For numerical rock physical simulations, a series of cores with variable porosities are needed to determine the relationship between the physical properties and porosity. In carbonate rocks, the secondary pore space including dissolution pores, caves and natural fractures is the key reservoir space, which makes the study of carbonate secondary porosity very important. To achieve the variation of porosities in one rock sample, based on CT scanned digital cores, according to the physical and chemical properties of carbonate rocks, several mathematical methods are chosen to simulate the variation of secondary pore space. We use the erosion and dilation operations of mathematical morphology method to simulate the pore space changes of dissolution pores and caves. We also use the Fractional Brownian Motion model to generate natural fractures with different widths and angles in digital cores to simulate fractured carbonate rocks. The morphological opening-and-closing operations in mathematical morphology method are used to simulate distribution of fluid in the pore space. The established 3D digital core models with different secondary porosities and water saturation status can be used in the study of the physical property numerical simulations of carbonate reservoir rocks.
Isotope Geochemistry of Possible Terrestrial Analogue for Martian Meteorite ALH84001

NASA Technical Reports Server (NTRS)

Mojzsis, Stephen J.

2000-01-01

We have studied the microdomain oxygen and carbon isotopic compositions by SIMS of complex carbonate rosettes from spinel therzolite xenoliths, hosted by nepheline basanite, from the island of Spitsbergen (Norway). The Quaternary volcanic rocks containing the xenoliths erupted into a high Arctic environment and through relatively thick continental crust containing carbonate rocks. We have attempted to constrain the sources of the carbonates in these rocks by combined O-18/O-16 and C-13/C-12 ratio measurements in 25 micron diameter spots of the carbonate and compare them to previous work based primarily on trace-element distributions. The origin of these carbonates can be interpreted in terms of either contamination by carbonate country rock during ascent of the xenoliths in the host basalt, or more probably by hydrothermal processes after emplacement. The isotopic composition of these carbonates from a combined delta.18O(sub SMOW) and delta.13C(sub PDB) standpoint precludes a primary origin of these minerals from the mantle. Here a description is given of the analysis procedure, standardization of the carbonates, major element compositions of the carbonates measured by electron microprobe, and their correlated C and O isotope compositions as measured by ion microprobe. Since these carbonate rosettes may represent a terrestrial analogue to the carbonate "globules" found in the martian meteorite ALH84001 interpretations for the origin of the features found in the Spitsbergen may be of interest in constraining the origin of these carbonate minerals on Mars.
Characterization of Endolithic Culturable Microbial Communities in Carbonate Rocks from a Typical Karst Canyon in Guizhou (China).

PubMed

Tang, Yuan; Cheng, Jian-Zhong; Lian, Bin

2017-01-02

The endolithic environment is a ubiquitous habitat for microorganisms and a critical interface between biology and geology. In this study, a culture-based method and the phylogenetic analysis based on 16S rRNA and internal transcribed spacer (ITS) sequences were used to investigate the diversity of endolithic bacteria and fungi in two main types of carbonate rocks (namely dolomite and limestone) from Nanjiang Canyon in Guizhou karst area, China. The results of bacterial diversity indicated that all bacteria isolated from dolomite and limestone rocks were divided into 4 bacterial groups, including Proteobacteria, Actinobacteria, Firmicutes and Bacteroidetes. For these two kinds of rocks, Proteobacteria was the first dominant group, and Gammaproteobacteria occupied the greatest proportion which might be closely related to Pseudomonas in phylogeny to be the most dominant genera after isolation. Actinobacteria and Bacillus bacteria were also widespread in these two kinds of rock environments. There were only 9 and 8 strains of fungi isolated from dolomite and limestone respectively, which all belonged to Ascomycota. To the best of our knowledge, this is the first report on diversity of endolithic culturable bacteria and fungi in carbonate rocks in Guizhou karst region. These microorganisms may play an important and unprecedented role in the carbonate rock weathering during the long history of geological evolution.
Numerical investigation on the expansion of supercritical carbon dioxide jet

NASA Astrophysics Data System (ADS)

Lv, Q.; Long, X. P.; Kang, Y.; Xiao, L. Z.; Wu, W.

2013-12-01

Supercritical carbon dioxide (SC-CO2) fluid is characterized by low rock breaking threshold pressure and high rock breaking rate. Meanwhile, SC-CO2 fluid has relatively low viscosity near to gas and high density near to liquid. So, it has great advantages in drilling and rock breaking over water. In this paper, numerical study of SC-CO2 flowing through a nozzle is presented. The purpose of this simulation is to ascertain why the SC-CO2 jet flow has better ability in drilling and rock breaking than the water jet flow. The simulation model was controlled by the RANS equations together with the continuity equation as well as the energy equation. The realizable k-epsilon turbulence model was adopted to govern the turbulent characteristics. Pressure boundary conditions were applied to the inlet and outlet boundary. The properties of carbon dioxide and water were described by UDF. It is found that: (1) under the same boundary conditions, the decay of dimensionless central axial velocity and dynamic pressure of water is quicker than that of the SC-CO2, and the core length of SC-CO2 jet is about 4.5 times of the nozzle diameter, which is 1 times longer than that of the water; (2) With the increase of inlet pressure or the decrease of outlet pressure, the dimensionless central axial velocity and dynamic pressure attenuation of water keeps the same, while the decay of central axial velocity of SC-CO2 turns gentle; (3) the change of central axial temperature of SC-CO2 is more complex than that of the water.
The zinc stable isotope signature of waste rock drainage in Arctic Canada

NASA Astrophysics Data System (ADS)

Matthies, Romy; Blowes, David

2014-05-01

Leachate emerging from a pilot-scale waste rock pile of the Diavik diamond mine, Northwest Territories, was monitored. The well-characterized waste rock consists of granite, pegmatitic granite and biotite schist with an average total sulfur and carbonate carbon concentration of 0.053 and 0.027 wt. %, respectively. During the field seasons of 2011 and 2012, the Zn stable isotope footprint was characterized alongside standard monitoring parameters. pH ranged between 4.3 and 6.8 and carbonate alkalinity was low or undetectable. Al and Fe concentrations averaged 6.78 mg L-1 and 175 µg L-1, respectively. The pH and metal mobility were governed by sulfide oxidation and sorption and co-precipitation onto iron and aluminium hydroxides. The main processes controlling zinc mobility in the range of 0.4 and 4.7 mg L-1 was the oxidative dissolution of sphalerite (ZnS) in the biotite schist and the attenuation of zinc onto secondary iron and aluminium hydroxides and desorption upon the pH declining below the pHpzc. The isotope ratios between -0.16 and +0.19 ‰ (δ66Zn, avg = +0.05 ‰, n = 43) are consistent with values reported from other sphalerite containing deposits. Zn isotope ratios and concentrations were largely uncorrelated suggesting that the processes affecting Zn mobility had little or no impact on the Zn isotope signature. Data indicate, that the Zn isotope ratios of the waste rock leachate may be used as a fingerprint to track anthropogenic, mine-derived Zn sources under varying environmental conditions.
Transformation of Serpentinite to Listvenite as Recorded in the Vein History of Rocks From Oman Drilling Project Hole BT1B

NASA Astrophysics Data System (ADS)

Manning, C. E.; Kelemen, P. B.; Michibayashi, K.; Harris, M.; Urai, J. L.; de Obeso, J. C.; Jesus, A. P. M.; Zeko, D.

2017-12-01

Oman Drilling Project Hole BT1B intersected 191 m of listvenite (magnesite + quartz rock) and serpentinite in the hanging wall of the basal thrust of the Oman ophiolite. Recovery was 100%. Listvenite is the dominant lithology in the upper plate rocks (166 m). Its shows wide color and textural variation, including pseudomorphic replacement of serpentinized peridotite. Serpentinite was encountered in two main contiguous intervals totaling 25 m. In light of the strongly metasomatic nature for the origin of listvenite, a substantial portion of the core description effort was dedicated to characterization of the complex veining history recorded in the hole. Dense veining is recorded in both lithologies. The density of <1 mm veins is >200/m. The density of veins >1 mm was 50-100/m, with somewhat higher densities recorded in serpentinite than in listvenite. In order of oldest to youngest, the main vein types in serpentinite are microscopic mesh-textured serpentine veins, macroscopic serpentine veins, carbonate-oxide veins, and carbonate veins. The vein paragenesis in listvenite is: early carbonate-oxide veins, followed by carbonate and carbonate-quartz veins, then late carbonate veins. The carbonate-oxide and carbonate veins are shared by the lithologies and hold clues to the transformation of ultramafic rocks to listvenite. Carbonate-oxide veins form a distinctive set that is interpreted to be the earliest record of carbonate formation in serpentinite. They contain Fe-oxide, usually hematite, on a medial line, with antitaxial magnesite crystals growing outward and showing terminations against wall rock minerals. Antitaxial textures may be evidence of positive reaction volumes. In serpentinite, secondary serpentine after earlier serpentine is common at vein margins. Carbonate-oxide veins are the earliest observed in listvenite, where they may form isolated veins to dense, aligned networks that impart a foliated texture. In some cases, they appear to predate replacement of serpentine by microcrystalline quartz. Both lithologies record later, coarser, through going carbonate ± quartz veins. Preliminary vein petrology in BT1B rocks indicates that fracture formation and filling by secondary minerals is integral to the metasomatic replacement of altered peridotite by listvenite.
Diversity of endolithic fungal communities in dolomite and limestone rocks from Nanjiang Canyon in Guizhou karst area, China.

PubMed

Tang, Yuan; Lian, Bin

2012-06-01

The endolithic environment, the tiny pores and cracks in rocks, buffer microbial communities from a number of physical stresses, such as desiccation, rapid temperature variations, and UV radiation. Considerable knowledge has been acquired about the diversity of microorganisms in these ecosystems, but few culture-independent studies have been carried out on the diversity of fungi to date. Scanning electron microscopy of carbonate rock fragments has revealed that the rock samples contain certain kinds of filamentous fungi. We evaluated endolithic fungal communities from bare dolomite and limestone rocks collected from Nanjiang Canyon (a typical karst canyon in China) using culture-independent methods. Results showed that Ascomycota was absolutely dominant both in the dolomite and limestone fungal clone libraries. Basidiomycota and other eukaryotic groups (Bryophyta and Chlorophyta) were only detected occasionally or at low frequencies. The most common genus in the investigated carbonate rocks was Verrucaria. Some other lichen-forming fungi (e.g., Caloplaca, Exophiala, and Botryolepraria), Aspergillus, and Penicillium were also identified from the rock samples. The results provide a cross-section of the endolithic fungal communities in carbonate rocks and help us understand more about the role of microbes (fungi and other rock-inhabiting microorganisms) in rock weathering and pedogenesis.
Calcite Decarbonation and its Influence on the Mechanical Behaviour of Carbonate-bearing Faults

NASA Astrophysics Data System (ADS)

Carpenter, Brett; Collettini, Cristiano; Mollo, Silvio; Viti, Cecilia

2014-05-01

Calcite decarbonation has been identified as one of the important, thermally-activated physicochemical processes that are triggered by temperature rise during fast fault motion. This process has been observed in the laboratory during high-velocity friction experiments where the dynamic weakening that occurs for carbonate-rich gouges is strictly controlled by the thermal decomposition of calcite. Furthermore, this process has also been identified along ancient, exhumed faults and is an important indicator of seismic slip. The thermally-induced decarbonation (CaCO3 → CaO + CO2) and microcracking (due to thermal expansion) of calcite are likely to be primary mechanisms in controlling the mechanical and hydrologic properties of carbonate rocks. In addition, the process and products of decarbonation will likely exert significant influence on the behaviour of faults at both geologic and earthquake time scales by causing changes in (1) the effective normal stress on the fault and (2) the frictional behaviour of material within it. Due to the paucity of scientific information on the effects of decarbonation and thermal microcracking on the mechanical properties of carbonate fault rocks, we present results from experiments performed on portlandite (>90 wt.%), a hydrous mineral formed by the recombination of CaO and water, and stable product of the decarbonation reaction. We produced portlandite by thermally-treating powdered Carrara Marble (calcite >98 wt.%) in the laboratory at 1100 °C under air buffering conditions. We then sheared gouge layers of this water-reacted, decarbonation product under saturated conditions at room temperature. These tests were designed to evaluate the frictional strength, stability, and healing behaviour of portlandite-bearing rocks to better understand how its presence affects fault mechanics. Our data indicate that the conversion of calcite to portlandite, results in a distinct change in the mechanical behaviour of the fault gouge. The difference in frictional strength, between marble and portlandite, increases from 0µ to 0.4µ as the normal stress is increased from 1 to 50 MPa. Additionally, at the low shearing rates of 0.1 and 0.3 µm/s, portlandite fails through stick-slip motion whereas calcite slides stably. Furthermore, we observe power-law type healing in portlandite that results in a dramatic increase in static frictional strength of ~0.2 µ over a relatively short hold time of 3000s. We suggest that decarbonated fault patches are (1) frictionally weaker, (2) more frictionally unstable, and (3) likely to regain their frictional strength more quickly, than patches in pure carbonate rocks. Under water-saturated conditions, the occurrence of portlandite and other hydrous minerals is undoubtedly the key for interpreting changes in the mechanical behaviour, both transient and long-term, of decarbonated faults.
Geochemistry of primary-carbonate bearing K-rich igneous rocks in the Awulale Mountains, western Tianshan: Implications for carbon-recycling in subduction zone

NASA Astrophysics Data System (ADS)

Yang, Wu-Bin; Niu, He-Cai; Shan, Qiang; Chen, Hua-Yong; Hollings, Pete; Li, Ning-Bo; Yan, Shuang; Zartman, Robert E.

2014-10-01

Arc magmatism plays an important role in the recycling of subducted carbon and returning it to the surface. However, the transfer mechanisms of carbon are poorly understood. In this study, the contribution of subducted carbonate-rich sediments to the genesis of the carbonate-bearing K-rich igneous rocks from western Tianshan was investigated. Four key triggers are involved, including sediments subduction, slab decarbonation, partial melting and magma segregation. The globular carbonate ocelli show C-O isotope signatures intermediate between oceanic sediments and mantle, suggesting that the carbon of the primary carbonate ocelli was derived from recycled subducted sediments in the mantle. Decarbonation of the subducted slab is regarded as the primary agent to carbonize the mantle wedge. Geochemical features indicate that the carbonate ocelli are primary, and that the parental K- and carbon-rich mafic alkaline magma was derived from partial melting of carbonated mantle wedge veined with phlogopite. Major and trace element compositions indicate that globular carbonate ocelli hosted in the Bugula K-rich igneous rocks are calcio-carbonate and formed primarily by segregation of the differentiated CO2-rich alkaline magma after crystallization fractionation. The K-rich alkaline magma, which formed from partial melting of metasomatized (i.e., phlogopite bearing) mantle wedge in the sub-arc region, is a favorable agent to transport subducted carbon back to the Earth's surface during carbon recycling in subduction zones, because of the high CO2 solubility in alkaline mafic magma. We therefore propose a model for the petrogenesis of the carbonate-bearing K-rich igneous rocks in western Tianshan, which are significant for revealing the mechanism of carbon recycling in subduction zones.
A High-Resolution Multitechniques Approach to Characterize Bio-Organo-Mineral Associations Within Rock Samples: Tracking Biological vs Abiotic Processes? Towards a Better Understanding of the Deep Carbon Cycle.

NASA Astrophysics Data System (ADS)

Pisapia, C.

2015-12-01

Among all elements, carbon plays one of the major roles for the sustainability of life on Earth. Past considerations of the carbon cycle have mainly focused on surface processes occurring at the atmosphere, oceans and shallow crustal environments. By contrast, little is known about the Deep Carbon cycle whereas both geochemical and biological processes may induce organic carbon production and/or consumption at depth. Indeed, the nowadays-recognized capability of geochemical processes such as serpentinization to generate abiotic organic compounds as well as the existence of a potentially important intraterrestrial life raises questions about the limit of biotic/abiotic carbon on Earth's deep interior and how it impacts global biogeochemical cycles. It is then mandatory to increase our knowledge on the nature and extent of carbon reservoirs along with their sources, sinks and fluxes in the subsurface. This implies to be able to finely characterize organomineral associations within crustal rocks although it might be hampered by the scarceness and heterogeneous micrometric spatial distribution of organic molecules in natural rocks. We then developed an in situ analytical strategy based on the combination of high-resolution techniques to track organic molecules at the pore level in natural rocks and to determine their biological or abiotic origin. We associated classical high-resolution techniques and synchrotron-based imaging techniques in order to characterize their nature and localization (SEM/TEM, coupled CLSM/Raman spectroscopy, Tof-SIMS) along with their 3D-distribution relatively to mineral phases (S-FTIR, S-DeepUV, XANES, Biphoton microscopy). The effectiveness of this approach to shed light on the speciation and nature of carbon in subsurface environments will be illustrated through the study of (i) subsurface ecosystems and abiotic organic carbon within ultramafic rocks of the oceanic lithosphere as putative analogs for the nature and functioning of primitive ecosystems on Earth and of (ii) ecosystems inhabiting Archean craton and potentially playing a role in punk-rock karstification processes and rocks weathering.
Carbon Retention and Isotopic Evolution in Deeply Subducted Sediments: Evidence from the Italian Alps

NASA Astrophysics Data System (ADS)

Cook-Kollars, J.; Bebout, G. E.; Agard, P.; Angiboust, S.

2012-12-01

Subduction-zone metamorphism of oceanic crust and carbonate-rich seafloor sediments plays an important regulatory role in the global C cycle by controlling the fraction of subducting C entering long-term storage in the mantle and the fraction of subducting C emitted into the atmosphere in arc volcanic gases. Modeling studies suggest that the extent of decarbonation of subducting sediments could be strongly affected by extents of infiltration by external H2O-rich fluids and that, in cool subduction zones, the dehydration of subducting oceanic slabs may not release sufficient H2O to cause significant decarbonation of overlying sediments [Gorman et al. (2006), G-cubed; Hacker (2008), G-cubed]. Metasedimentary suites in the Western Alps (sampled from the Schistes Lustres, Zermatt-Saas ophiolite, and at Lago di Cignana) were subducted to depths corresponding to 1.5-3.2 GPa, over a range of peak temperatures of 350-600°C, and are associated with HP/UHP-metamorphosed Jurassic ophiolitic rocks [Agard et al. (2001), Bull. soc. geol. France; Frezzotti et al. (2011), Nature Geoscience]. These metasedimentary suites are composed of interlayered metapelites and metacarbonates and represent a range of peak P-T conditions experienced in modern, relatively cool subduction zones. Integrated petrologic and isotopic study of these rocks allows an analysis of decarbonation and isotopic exchange among oxidized and reduced C reservoirs along prograde subduction-zone P-T paths. Petrographic work on Schistes Lustres metacarbonates indicates only minor occurrences of calc-silicate phases, consistent with the rocks having experienced only very minor decarbonation during prograde metamorphism. Carbonate δ13CVPDB values (-1.5 to 1‰) are similar to values typical of marine carbonates. Higher grade, UHP-metamorphosed carbonates at Cignana show mineralogic evidence of decarbonation; however, the δ13C of the calcite in these samples remains similar to that of marine carbonate. With increasing grade, metapelitic carbonaceous matter shows an increase in δ13CVPDB, ranging from about -25‰ in low-grade Schistes Lustres samples to -16‰ in the highest-grade Cignana samples. Carbonate in the entire suite shows decrease in δ18OSMOW, from marine carbonate values > 25‰ to values of 17-22‰ independent of the carbonate content of the rocks. This shift could possibly be explained by isotopic exchange with silicate phases in the same rocks [Henry et al. (1996), Chem. Geol.]. Metapelitic rocks in this suite experienced moderate amounts of dehydration (20-50%) largely related to breakdown of chlorite and carpholite [Bebout et al. (in press), Chem. Geol. (abstract in this session); Angiboust and Agard (2010), Lithos], conceivably providing a source for infiltrating H2O-rich fluids producing negative shifts in calcite δ18O in interlayered metacarbonates. These results indicate that relatively little decarbonation occurred in carbonate-bearing sediments subducted to depths greater than 100 km, arguing against any model of extensive decarbonation driven by infiltration of the sediments by H2O-rich fluids released from mafic and ultramafic parts of the underlying subducting slab. This study provides field evidence for the efficient retention of C in subducting shale-carbonate sequences through forearc depths, potentially affecting the C budget and isotopic evolution of the deeper mantle.
Publications - GMC 208 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 208 Publication Details Title: HRZ total organic carbon and rock-eval data from cuttings of , HRZ total organic carbon and rock-eval data from cuttings of Colville basin and Arctic Foothills (117.0 K) Keywords Total Organic Carbon Top of Page Department of Natural Resources, Division of
Publications - GMC 205 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 205 Publication Details Title: Total organic carbon, rock-eval, and gas chromatograms from for more information. Bibliographic Reference Unknown, 1992, Total organic carbon, rock-eval, and gas Information gmc205.pdf (272.0 K) Keywords Total Organic Carbon Top of Page Department of Natural Resources
A First Look at Airborne Imaging Spectrometer (AIS) Data in an Area of Altered Volcanic Rocks and Carbonate Formations, Hot Creek Range, South Central Nevada

NASA Technical Reports Server (NTRS)

Feldman, S. C.; Taranik, J. V.; Mouat, D. A.

1985-01-01

Three flight lines of Airborne Imaging Spectrometer (AIS) data were collected in 128 bands between 1.2 and 2.4 microns in the Hot Creek Range, Nevada on July 25, 1984. The flight lines are underlain by hydrothermally altered and unaltered Paleozoic carbonates and Tertiary rhyolitic to latitic volcanics in the Tybo mining district. The original project objectives were to discriminate carbonate rocks from other rock types, to distinguish limestone from dolomite, and to discriminate carbonate units from each other using AIS imagery. Because of high cloud cover over the prime carbonate flight line and because of the acquisition of another flight line in altered and unaltered volcanics, the study has been extended to the discrimination of alteration products. In an area of altered and unaltered rhyolites and latites in Red Rock Canyon, altered and unaltered rock could be discriminated from each other using spectral features in the 1.16 to 2.34 micron range. The altered spectral signatures resembled montmorillonite and kaolinite. Field samples were gathered and the presence of montmorillonite was confirmed by X-ray analysis.
Salt deposits in Los Medanos area, Eddy and Lea counties, New Mexico

USGS Publications Warehouse

Jones, C.L.; with sections on Ground water hydrology, Cooley; and Surficial Geology, Bachman

1973-01-01

The salt deposits of Los Medanos area, in Eddy and Lea Counties, southeastern New Mexico, are being considered for possible use as a receptacle for radioactive wastes in a pilot-plant repository. The salt deposits of the area. are in three evaporite formations: the Castile, Salado, and Rustler Formations, in ascending order. The three formations are dominantly anhydrite and rock salt, but some gypsum, potassium ores, carbonate rock, and fine-grained clastic rocks are present. They have combined thicknesses of slightly more than 4,000 feet, of which roughly one-half belongs to the Salado. Both the Castile and the Rustler are-richer in anhydrite-and poorer in rock salt-than the Salado, and they provide this salt-rich formation with considerable Protection from any fluids which might be present in underlying or overlying rocks. The Salado Formation contains many thick seams of rock salt at moderate depths below the surface. The rock salt has a substantial cover of well-consolidated rocks, and it is very little deformed structurally. Certain geological details essential for Waste-storage purposes are unknown or poorly known, and additional study involving drilling is required to identify seams of rock salt suitable for storage purposes and to establish critical details of their chemistry, stratigraphy, and structure.
Stromatolite- and coated-grain-bearing carbonate rocks of the western Brooks Range: A section in Geologic studies in Alaska by the U.S. Geological Survey during 1987

USGS Publications Warehouse

Dumoulin, Julie A.

1988-01-01

Carbonate rocks characterized by locally abundant stromatolites and coated grains have been found at several localities in the Baird Mountains and Ambler River quadrangles (fig. 1). These rocks are part of a belt of metasedimentary and metaigneous rocks that constitutes the southwestern flank of the Brooks Range; all are included in the parautochthon (Schwatka sequence) of Mayfield and others (1983). The rocks have been deformed and metamorphosed to blueschist and greenschist facies, but primary textures and sedimentary structures are locally well preserved.
Alteration of the Carbon and Nitrogen Isotopic Composition in the Martian Surface Rocks Due to Cosmic Ray Exposure

NASA Technical Reports Server (NTRS)

Pavlov, A. A.; Pavlov, A. K.; Ostryakov, V. M.; Vasilyev, G. I.; Mahaffy, P.; Steele, A.

2014-01-01

C-13/C-12 and N-15/N-14 isotopic ratios are pivotal for our understanding of the Martian carbon cycle, history of the Martian atmospheric escape, and origin of the organic compounds on Mars. Here we demonstrate that the carbon and nitrogen isotopic composition of the surface rocks on Mars can be significantly altered by the continuous exposure of Martian surface to cosmic rays. Cosmic rays can effectively produce C-13 and N-15 isotopes via spallation nuclear reactions on oxygen atoms in various Martian rocks. We calculate that in the top meter of the Martian rocks, the rates of production of both C-13 and N-15 due to galactic cosmic rays (GCRs) exposure can vary within 1.5-6 atoms/cm3/s depending on rocks' depth and chemical composition. We also find that the average solar cosmic rays can produce carbon and nitrogen isotopes at a rate comparable to GCRs in the top 5-10 cm of the Martian rocks. We demonstrate that if the total carbon content in a surface Martian rock is <10 ppm, then the "light," potentially "biological" C-13/C-12 ratio would be effectively erased by cosmic rays over 3.5 billion years of exposure. We found that for the rocks with relatively short exposure ages (e.g., 100 million years), cosmogenic changes in N-15/N-14 ratio are still very significant. We also show that a short exposure to cosmic rays of Allan Hills 84001 while on Mars can explain its high-temperature heavy nitrogen isotopic composition (N-15/N-14). Applications to Martian meteorites and the current Mars Science Laboratory mission are discussed.

The effect of heated vapor-phase acidification on organic carbon concentrations and isotopic values in geologic rock samples

NASA Astrophysics Data System (ADS)

Wang, R. Z.; West, A. J.; Yager, J. A.; Rollins, N.; Li, G.; Berelson, W.

2016-12-01

Carbon signatures recorded in the modern and geologic rock record can give insight on the Earth's carbon cycle through time. This is especially true for organic carbon (OC), which can help us understand how the biosphere has evolved over Earth's history. However, carbon recorded in rocks is a combination of OC and inorganic carbon (IC) mostly in the form of carbonate minerals. To measure OC, IC must therefore first be removed through a process called "decarbonation." This is often done through a leaching process with hydrochloric acid (HCl). However, three well known problems exist for the decarbonation process: 1) Incomplete removal of IC, 2) Unintentional removal of OC, and 3) Addition of false carbon blank. Currently, vapor (gas) phase removal of OC is preferred to liquid phase treatment because it has been shown that OC is lost to solubilization during liquid phase acidification. Vapor phase treatment is largely thought to avoid the problem of OC loss, but this has not yet been rigorously investigated. This study investigates that assumption and shows that vapor phase treatment can cause unintentional OC loss. We show that vapor phase treatment must be sensitive to rock type and treatment length to produce robust OC isotopic measurements and concentrations.
Geochemistry of Eagle Ford group source rocks and oils from the first shot field area, Texas

USGS Publications Warehouse

Edman, Janell D.; Pitman, Janet K.; Hammes, Ursula

2010-01-01

Total organic carbon, Rock-Eval pyrolysis, and vitrinite reflectance analyses performed on Eagle Ford Group core and cuttings samples from the First Shot field area, Texas demonstrate these samples have sufficient quantity, quality, and maturity of organic matter to have generated oil. Furthermore, gas chromatography and biomarker analyses performed on Eagle Ford Group oils and source rock extracts as well as weight percent sulfur analyses on the oils indicate the source rock facies for most of the oils are fairly similar. Specifically, these source rock facies vary in lithology from shales to marls, contain elevated levels of sulfur, and were deposited in a marine environment under anoxic conditions. It is these First Shot Eagle Ford source facies that have generated the oils in the First Shot Field. However, in contrast to the generally similar source rock facies and organic matter, maturity varies from early oil window to late oil window in the study area, and these maturity variations have a pronounced effect on both the source rock and oil characteristics. Finally, most of the oils appear to have been generated locally and have not experienced long distance migration.
Occurrence model for volcanogenic beryllium deposits: Chapter F in Mineral deposit models for resource assessment

USGS Publications Warehouse

Foley, Nora K.; Hofstra, Albert H.; Lindsey, David A.; Seal, Robert R.; Jaskula, Brian W.; Piatak, Nadine M.

2012-01-01

Current global and domestic mineral resources of beryllium (Be) for industrial uses are dominated by ores produced from deposits of the volcanogenic Be type. Beryllium deposits of this type can form where hydrothermal fluids interact with fluorine and lithophile-element (uranium, thorium, rubidium, lithium, beryllium, cesium, tantalum, rare earth elements, and tin) enriched volcanic rocks that contain a highly reactive lithic component, such as carbonate clasts. Volcanic and hypabyssal high-silica biotite-bearing topaz rhyolite constitutes the most well-recognized igneous suite associated with such Be deposits. The exemplar setting is an extensional tectonic environment, such as that characterized by the Basin and Range Province, where younger topaz-bearing igneous rock sequences overlie older dolomite, quartzite, shale, and limestone sequences. Mined deposits and related mineralized rocks at Spor Mountain, Utah, make up a unique economic deposit of volcanogenic Be having extensive production and proven and probable reserves. Proven reserves in Utah, as reported by the U.S. Geological Survey National Mineral Information Center, total about 15,900 tons of Be that are present in the mineral bertrandite (Be4Si2O7(OH)2). At the type locality for volcanogenic Be, Spor Mountain, the tuffaceous breccias and stratified tuffs that host the Be ore formed as a result of explosive volcanism that brought carbonate and other lithic fragments to the surface through vent structures that cut the underlying dolomitic Paleozoic sedimentary rock sequences. The tuffaceous sediments and lithic clasts are thought to make up phreatomagmatic base surge deposits. Hydrothermal fluids leached Be from volcanic glass in the tuff and redeposited the Be as bertrandite upon reaction of the hydrothermal fluid with carbonate clasts in lithic-rich sections of tuff. The localization of the deposits in tuff above fluorite-mineralized faults in carbonate rocks, together with isotopic evidence for the involvement of magmatic water in an otherwise meteoric water-dominated hydrothermal system, indicate that magmatic volatiles contributed to mineralization. At the type locality, hydrothermal alteration of dolomite clasts formed layered nodules of calcite, opal, fluorite, and bertrandite, the latter occurring finely intergrown with fluorite. Alteration assemblages and elemental enrichments in the tuff and surrounding volcanic rocks include regional diagenetic clays and potassium feldspar and distinctive hydrothermal halos of anomalous fluorine, lithium, molybdenum, niobium, tin, and tantalum, and intense potassium feldspathization with sericite and lithium-smectite in the immediate vicinity of Be ore. Formation of volcanogenic Be deposits is due to the coincidence of multiple factors that include an appropriate Be-bearing source rock, a subjacent pluton that supplied volatiles and heat to drive convection of meteoric groundwater, a depositional site characterized by the intersection of normal faults with permeable tuff below a less permeable cap rock, a fluorine-rich ore fluid that facilitated Be transport (for example, BeF42- complex), and the existence of a chemical trap that caused fluorite and bertrandite to precipitate at the former site of carbonate lithic clasts in the tuff.
Heavy metals and organic carbon in sediments from the Tuy River basin, Venezuela.

PubMed

Mogollón, J L; Ramirez, A J; Guillén, R B; Bifano, C

1990-12-01

The Tuy River basin, located in north-central Venezuela with an annual average temperature of 27°C and precipitation of 140 cm, was selected to conduct a geochemical study of bottom sediments, with the object of establishing the natural and human influences in the abundance and distribution of Fe, Mn, Cr, Co, Cu, Ni, Pb, Zn and organic carbon. The basin is lithologically divided into two sub-basins, north and south. The north sub-basin drains a iow-grade metasedimentary terrain with a population density of 800 persons km(-2) and approximateiy 600 industrial sites, while the south sub-basin in underlain by metavolcanic and ultramafic rocks, with a population density of less than 10 persons km(-2).Stream bottom sediment samples (150) were collected during the years of 1979-1986 in 16 unpolluted sites and 13 polluted sites. The sediments were air dried at room temperature and sieved through a 120 stainless steel mesh (125 μm). Samples of grain size smaller than 125 μm were analysed, the heavy metals being determined by atomic absorption spectrometry and the organic carbon (Corg) by dry combustion.The higher concentrations of heavy metals and organic carbon found in the pristine areas were in the south sub-basin, especially in those areas with higher annual precipitation and tropical forest. This indicated that the metavolcanic and ultramafic rocks yield higher concentrations of heavy metals than the metasedimentary rocks. It was also noted that the higher concentrations of Cr and Ni are associated with the ultramafic rocks. The results obtained from the sediment samples collected in the polluted sites showed that the elements Pb, Zn and Corg are enriched up to 4 times as a result of ail the human activities taking place in the basin. Organic carbon is an excellent indicator of domestic wastewater, Pb and Zn are good indicators of the automotive traffic and industrial effluents. The concentrations of each heavy metal did not show any significant correlation with grain size fractions; however, the concentration of organic carbon did show a negative correlation with grain size. The lithological, climatic and vegetation influence in the abundance of heavy metals and organic carbon in stream sediments clearly indicates the necessity of establishing background levels for the area under study when carrying out studies in environmental geochemistry.
Publications - GMC 285 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 285 Publication Details Title: Total organic carbon (TOC), rock-eval, and gas chromatography , Total organic carbon (TOC), rock-eval, and gas chromatography of core (8846.2'-13508') from the Husky Report Information gmc285.pdf (4.5 M) Keywords Total Organic Carbon Top of Page Department of Natural
New insights into the nation's carbon storage potential

USGS Publications Warehouse

Warwick, Peter D.; Zhu, Zhi-Liang

2012-01-01

Carbon sequestration is a method of securing carbon dioxide (CO2) to prevent its release into the atmosphere, where it contributes to global warming as a greenhouse gas. Geologic storage of CO2 in porous and permeable rocks involves injecting high-pressure CO2 into a subsurface rock unit that has available pore space. Biologic carbon sequestration refers to both natural and anthropogenic processes by which CO2 is removed from the atmosphere and stored as carbon in vegetation, soils, and sediments.
Rock Outcrops Redistribute Organic Carbon and Nutrients to Nearby Soil Patches in Three Karst Ecosystems in SW China

PubMed Central

Wang, Dianjie; Shen, Youxin; Li, Yuhui; Huang, Jin

2016-01-01

Emergent rock outcrops are common in terrestrial ecosystems. However, little research has been conducted regarding their surface function in redistributing organic carbon and nutrient fluxes to soils nearby. Water that fell on and ran off 10 individual rock outcrops was collected in three 100 × 100 m plots within a rock desertification ecosystem, an anthropogenic forest ecosystem, and a secondary forest ecosystem between June 2013 and June 2014 in Shilin, SW China. The concentrations of total organic carbon (TOC), total nitrogen (N), total phosphorus (P), and potassium (K) in the water samples were determined during three seasons, and the total amounts received by and flowing out from the outcrops were calculated. In all three ecosystems, TOC and N, P, and K were found throughout the year in both the water received by and delivered to nearby soil patches. Their concentrations and amounts were generally greater in forested ecosystems than in the rock desertification ecosystem. When rock outcrops constituted a high percentage (≥ 30%) of the ground surface, the annual export of rock outcrop runoff contributed a large amount of organic carbon and N, P, and K nutrients to soil patches nearby by comparison to the amount soil patches received via atmospheric deposition. These contributions may increase the spatial heterogeneity of soil fertility within patches, as rock outcrops of different sizes, morphologies, and emergence ratios may surround each soil patch. PMID:27509199
Interpretation of well logs in a carbonate aquifer

USGS Publications Warehouse

MacCary, L.M.

1978-01-01

This report describes the log analysis of the Randolph and Sabial core holes in the Edwards aquifer in Texas, with particular attention to the principles that can be applied generally to any carbonate system. The geologic and hydrologic data were obtained during the drilling of the two holes, from extensive laboratory analysis of the cores, and from numerous geophysical logs run in the two holes. Some logging methods are inherently superiors to others for the analysis of limestone and dolomite aquifers. Three such systems are the dentistry, neutron, and acoustic-velocity (sonic) logs. Most of the log analysis described here is based on the interpretation of suites of logs from these three systems. In certain instances, deeply focused resistivity logs can be used to good advantage in carbonate rock studies; this technique is used to computer the water resistivity in the Randolph core hole. The rocks penetrated by the Randolph core hole are typical of those carbonates that have undergone very little solution by recent ground-water circulation. There are few large solutional openings; the water is saline; and the rocks are dark, dolomitic, have pore space that is interparticle or intercrystalline, and contain unoxidized organic material. The total porosity of rocks in the saline zone is higher than that of rocks in the fresh-water aquifer; however, the intrinsic permeability is much less in the saline zone because there are fewer large solutional openings. The Sabinal core hole penetrates a carbonate environment that has experienced much solution by ground water during recent geologic time. The rocks have high secondary porosities controlled by sedimentary structures within the rock; the water is fresh; and the dominant rock composition is limestone. The relative percentages of limestone and dolomite, the average matrix (grain) densities of the rock mixtures , and the porosity of the rock mass can be calculated from density, neutron, and acoustic logs. With supporting data from resistivity logs, the formation water quality can be estimated, as well as the relative cementation or tortuosity of the rock. Many of these properties calculated from logs can be verified by analysis of the core available from test holes drilled in the saline and fresh water zones.
Ocean alkalinity and the Cretaceous/Tertiary boundary

NASA Technical Reports Server (NTRS)

Caldeira, K. G.; Rampino, Michael R.

1988-01-01

A biogeochemical cycle model resolving ocean carbon and alkalinity content is applied to the Maestrichtian and Danian. The model computes oceanic concentrations and distributions of Ca(2+), Mg(2+), and Sigma-CO2. From these values an atmospheric pCO2 value is calculated, which is used to estimate rates of terrestrial weathering of calcite, dolomite, and calcium and magnesium silicates. Metamorphism of carbonate rocks and the subsequent outgassing of CO2 to the atmosphere are parameterized in terms of carbonate rock reservoir sizes, total land area, and a measure of overall tectonic activity, the sea-floor generation rate. The ocean carbon reservoir computed by the model is used with Deep Sea Drilling Project (DSDP) C-13 data to estimate organic detrital fluxes under a variety of ocean mixing rate assumptions. Using Redfield ratios, the biogenic detrital flux estimate is used to partition the ocean carbon and alkalinity reservoirs between the mixed layer and deep ocean. The calcite flux estimate and carbonate ion concentrations are used to determine the rate of biologically mediated CaCO3 titration. Oceanic productivity was severely limited for approximately 500 kyr following the K/T boundary resulting in significant increases in total ocean alkalinity. As productivity returned to the ocean, excess carbon and alkalinity was removed from the ocean as CaCO3. Model runs indicate that this resulted in a transient imbalance in the other direction. Ocean chemistry returned to near-equilibrium by about 64 mybp.
Isotopic studies of mariposite-bearing rocks from the south- central Mother Lode, California.

USGS Publications Warehouse

Kistler, R.W.; Dodge, F.C.W.; Silberman, M.L.

1983-01-01

Gold-bearing vein formation in the Mother Lode belt of the study area apparently occurred during the Early Cretaceous between 127 and 108 m.y. B.P. The hydrothermal fluids that carried the gold precipitated quartz and mariposite at approx 320oC, similar to the T of precipitation of gold-bearing quartz veins in the Allegheny district. The O- and H-isotopic composition calculated for the fluid indicate that it was similar to formation water or was metamorphic in origin. If the carbonate in the veins was in isotopic equilibrium with this same fluid, it apparently precipitated at a higher T of approx 400oC. The Sr in the carbonate is much less radiogenic than that in any known marine carbonate, but is similar in isotopic composition to that in metamorphosed mafic volcanic rocks of the general region. These mafic rocks could have been the source for the Sr in the hydrothermal veins. This observation supports the contention that the gold-mariposite-quartz-carbonate rocks were formed as an alteration product of serpentinite and other mafic igneous rocks.-A.P.
Ground penetrating radar imaging of cap rock, caliche and carbonate strata

USGS Publications Warehouse

Kruse, S.E.; Schneider, J.C.; Campagna, D.J.; Inman, J.A.; Hickey, T.D.

2000-01-01

Field experiments show ground penetrating radar (GPR) can be used to image shallow carbonate stratigraphy effectively in a variety of settings. In south Florida, the position and structure of cap rock cover on limestone can be an important control on surface water flow and vegetation, but larger scale outcrops (tens of meters) of cap rock are sparse. GPR mapping through south Florida prairie, cypress swamp and hardwood hammock resolves variations in thickness and structure of cap rock to ~3 m and holds the potential to test theories for cap rock-vegetation relationships. In other settings, carbonate strata are mapped to test models for the formation of local structural anomalies. A test of GPR imaging capabilities on an arid caliche (calcrete) horizon in southeastern Nevada shows depth penetration to ~2 m with resolution of the base of caliche. GPR profiling also succeeds in resolving more deeply buried (~5 m) limestone discontinuity surfaces that record subaerial exposure in south Florida. (C) 2000 Elsevier Science B.V. All rights reserved.Field experiments show ground penetrating radar (GPR) can be used to image shallow carbonate stratigraphy effectively in a variety of settings. In south Florida, the position and structure of cap rock cover on limestone can be an important control on surface water flow and vegetation, but larger scale outcrops (tens of meters) of cap rock are sparse. GPR mapping through south Florida prairie, cypress swamp and hardwood hammock resolves variations in thickness and structure of cap rock to approx. 3 m and holds the potential to test theories for cap rock-vegetation relationships. In other settings, carbonate strata are mapped to test models for the formation of local structural anomalies. A test of GPR imaging capabilities on an arid caliche (calcrete) horizon in southeastern Nevada shows depth penetration to approx. 2 m with resolution of the base of caliche. GPR profiling also succeeds in resolving more deeply buried (approx. 5 m) limestone discontinuity surfaces that record subaerial exposure in south Florida.
Investigation of Isotopic and Geochemical Evidence for an Active Planktonic Biota in the Precambrian

NASA Technical Reports Server (NTRS)

Kump, Lee R.

1997-01-01

The funded research was motivated by the earlier study of Burdett et al. (1990), who collected carbon and oxygen isotopic data from Paleoproterozoic rocks of the Northwest Territories from deep-and shallow-water facies of the Rocknest Platform. Their results displayed a possible decrease in (delta)C-13 with depth when arranged by increasing distance from the paleoshore. The most C-13-depleted samples were seafloor cements and fans from the underlying siliciclastic Odjick Formation, and slope carbonates of the Rocknest platform.
Interaction Between CO2-Rich Sulfate Solutions and Carbonate Reservoir Rocks from Atmospheric to Supercritical CO2 Conditions: Experiments and Modeling

NASA Astrophysics Data System (ADS)

Cama, J.; Garcia-Rios, M.; Luquot, L.; Soler Matamala, J. M.

2014-12-01

A test site for CO2 geological storage is situated in Hontomín (Spain) with a reservoir rock that is mainly composed of limestone. During and after CO2 injection, the resulting CO2-rich acid brine gives rise to the dissolution of carbonate minerals (calcite and dolomite) and gypsum (or anhydrite at depth) may precipitate since the reservoir brine contains sulfate. Experiments using columns filled with crushed limestone or dolostone were conducted under different P-pCO2 conditions (atmospheric: 1-10-3.5 bar; subcritical: 10-10 bar; and supercritical: 150-34 bar), T (25, 40 and 60 ºC) and input solution compositions (gypsum-undersaturated and gypsum-equilibrated solutions). We evaluated the effect of these parameters on the coupled reactions of calcite/dolomite dissolution and gypsum/anhydrite precipitation. The CrunchFlow and PhreeqC (v.3) numerical codes were used to perform reactive transport simulations of the experiments. Under the P-pCO2-T conditions, the volume of precipitated gypsum was smaller than the volume of dissolved carbonate minerals, yielding an increase in porosity (Δporosity up to ≈ 4%). A decrease in T favored limestone dissolution regardless of pCO2 owing to increasing undersaturation with decreasing temperature. However, gypsum precipitation was favored at high T and under atmospheric pCO2 conditions but not at high T and under 10 bar of pCO2 conditions. The increase in limestone dissolution with pCO2 was directly attributed to pH, which was more acidic at higher pCO2. Increasing pCO2, carbonate dissolution occurred along the column whereas it was localized in the very inlet under atmospheric conditions. This was due to the buffer capacity of the carbonic acid, which maintains pH at around 5 and keeps the solution undersaturated with respect to calcite and dolomite along the column. 1D reactive transport simulations reproduced the experimental data (carbonate dissolution and gypsum precipitation for different P-pCO2-T conditions). Drawing on reaction rate laws in the literature, we used the reactive surface area to fit the models to the experimental data. The values of the reactive surface area were much smaller than those calculated of the geometric areas.
Evaluation of the ground-water resources of parts of Lancaster and Berks Counties, Pennsylvania

USGS Publications Warehouse

Gerhart, J.M.; Lazorchick, G.J.

1984-01-01

Secondary openings in bedrock are the avenues for virtually all ground-water flow in a 626-sqare-mile area in Lancaster and Berks Counties, Pennsylvania. The number, size, and interconnection of secondary openings are functions of lithology, depth, and topography. Ground water actively circulates to depths of 150 to 300 feet below land surface. Total average annual ground-water recharge for the area is 388 million gallons per day, most of which discharges to streams from local, unconfined flow systems. A digital ground-water flow model was developed to simulate unconfined flow under several different recharge and withdrawal scenarios. On the basis of lithologic and hydrologic differences, the modeled area was sub-divided into 22 hydrogeologic units. A finite-difference grid with rectangular blocks, each 2,015 by 2,332 feet, was used. The model was calibrated under steady-state and transient conditions. The steady-state calibration was used to determine hydraulic conductivities and stream leakage coefficients and the transient calibration was used to determine specific yields. The 22 hydrogeologic units fall into four general lithologies: Carbonate rocks, metamorphic rocks, Paleozoic sedimentary rocks, and Triassic sedimentary rocks. Average hydraulic conductivity ranges from about 8.8 feet per day in carbonate units to about .5 feet per day in metamorphic units. The Stonehenge Formation (limestone) has the greatest average hydraulic conductivity--85.2 feet per day in carbonate units to about 0.11 feet per day in the greatest gaining-strem leakage coefficient--16.81 feet per day. Specific yield ranges from 0.06 to 0.09 in carbonate units, and is 0.02 to 0.015, and 0.012 in metamorphic, Paleozoic sedimentary, and Triassic sedimentary units, respectively. Transient simulations were made to determine the effects of four different combinations of natural and artificial stresses. Natural aquifer conditions (no ground-water withdrawals) and actual aquifer conditions (current ground-water withdrawals) were simulated for two years under normal seasonal and hypothetical drought (60-percent reduction in winter-spring recharge) conditions. In October, 6 months after the hypothetical drought, simulated declines in water-table altitude due to the drought occurred everywhere and ranged from a median of 3.6 feet in carbonate units to 8.7 feet in carbonate units. Simulated base flows for five major streams were reduced by 33 to 51 percent during the hypothetical drought. Also in October, maximum simulated declines in water-table altitude due to ground-water withdrawls ranged from 33 feet in carbonate units to 79 feet in Triassic sedimentary units. Simulated base flows for five major streams were reduced by the amount of ground water withdrawn. Finally, again in October, maximum simulated declines in water-table altitude due to the combination of hypothetical drought and ground-water withdrawls ranged from 38 feet in carbonate units to 109 feet in Triassic sedimentary units. Due to aquifer dewatering, simulated declines were as much as 24 feet greater than the sum of the separate simulated declines that were caused by hypothetical drought and ground-water withdrawals. Some of the greatest simulated declines were in well fields, operated by three municipalities that experienced water-supply problems during the 1980-81 drought.
Two-phase flow visualization under reservoir conditions for highly heterogeneous conglomerate rock: A core-scale study for geologic carbon storage.

PubMed

Kim, Kue-Young; Oh, Junho; Han, Weon Shik; Park, Kwon Gyu; Shinn, Young Jae; Park, Eungyu

2018-03-20

Geologic storage of carbon dioxide (CO 2 ) is considered a viable strategy for significantly reducing anthropogenic CO 2 emissions into the atmosphere; however, understanding the flow mechanisms in various geological formations is essential for safe storage using this technique. This study presents, for the first time, a two-phase (CO 2 and brine) flow visualization under reservoir conditions (10 MPa, 50 °C) for a highly heterogeneous conglomerate core obtained from a real CO 2 storage site. Rock heterogeneity and the porosity variation characteristics were evaluated using X-ray computed tomography (CT). Multiphase flow tests with an in-situ imaging technology revealed three distinct CO 2 saturation distributions (from homogeneous to non-uniform) dependent on compositional complexity. Dense discontinuity networks within clasts provided well-connected pathways for CO 2 flow, potentially helping to reduce overpressure. Two flow tests, one under capillary-dominated conditions and the other in a transition regime between the capillary and viscous limits, indicated that greater injection rates (potential causes of reservoir overpressure) could be significantly reduced without substantially altering the total stored CO 2 mass. Finally, the capillary storage capacity of the reservoir was calculated. Capacity ranged between 0.5 and 4.5%, depending on the initial CO 2 saturation.
Spatially-resolved isotopic study of carbon trapped in ∼3.43 Ga Strelley Pool Formation stromatolites

NASA Astrophysics Data System (ADS)

Flannery, David T.; Allwood, Abigail C.; Summons, Roger E.; Williford, Kenneth H.; Abbey, William; Matys, Emily D.; Ferralis, Nicola

2018-02-01

The large isotopic fractionation of carbon associated with enzymatic carbon assimilation allows evidence for life's antiquity, and potentially the early operation of several extant metabolic pathways, to be derived from the stable carbon isotope record of sedimentary rocks. Earth's organic carbon isotope record extends to the Late Eoarchean-Early Paleoarchean: the age of the oldest known sedimentary rocks. However, complementary inorganic carbon reservoirs are poorly represented in the oldest units, and commonly reported bulk organic carbon isotope measurements do not capture the micro-scale isotopic heterogeneities that are increasingly reported from younger rocks. Here, we investigated the isotopic composition of the oldest paired occurrences of sedimentary carbonate and organic matter, which are preserved as dolomite and kerogen within textural biosignatures of the ∼3.43 Ga Strelley Pool Formation. We targeted least-altered carbonate phases in situ using microsampling techniques guided by non-destructive elemental mapping. Organic carbon isotope values were measured by spatially-resolved bulk analyses, and in situ using secondary ion mass spectrometry to target microscale domains of organic material trapped within inorganic carbon matrixes. Total observed fractionation of 13C ranges from -29 to -45‰. Our data are consistent with studies of younger Archean rocks that host biogenic stromatolites and organic-inorganic carbon pairs showing greater fractionation than expected for Rubisco fixation alone. We conclude that organic matter was fixed and/or remobilized by at least one metabolism in addition to the CBB cycle, possibly by the Wood-Ljungdahl pathway or methanogenesis-methanotrophy, in a shallow-water marine environment during the Paleoarchean.
Mineral Dissolution and Precipitation due to Carbon Dioxide-Water-Rock Interactions: The Significance of Accessory Minerals in Carbonate Reservoirs (Invited)

NASA Astrophysics Data System (ADS)

Kaszuba, J. P.; Marcon, V.; Chopping, C.

2013-12-01

Accessory minerals in carbonate reservoirs, and in the caprocks that seal these reservoirs, can provide insight into multiphase fluid (CO2 + H2O)-rock interactions and the behavior of CO2 that resides in these water-rock systems. Our program integrates field data, hydrothermal experiments, and geochemical modeling to evaluate CO2-water-rock reactions and processes in a variety of carbonate reservoirs in the Rocky Mountain region of the US. These studies provide insights into a wide range of geologic environments, including natural CO2 reservoirs, geologic carbon sequestration, engineered geothermal systems, enhanced oil and gas recovery, and unconventional hydrocarbon resources. One suite of experiments evaluates the Madison Limestone on the Moxa Arch, Southwest Wyoming, a sulfur-rich natural CO2 reservoir. Mineral textures and geochemical features developed in the experiments suggest that carbonate minerals which constitute the natural reservoir will initially dissolve in response to emplacement of CO2. Euhedral, bladed anhydrite concomitantly precipitates in response to injected CO2. Analogous anhydrite is observed in drill core, suggesting that secondary anhydrite in the natural reservoir may be related to emplacement of CO2 into the Madison Limestone. Carbonate minerals ultimately re-precipitate, and anhydrite dissolves, as the rock buffers the acidity and reasserts geochemical control. Another suite of experiments emulates injection of CO2 for enhanced oil recovery in the Desert Creek Limestone (Paradox Formation), Paradox Basin, Southeast Utah. Euhedral iron oxyhydroxides (hematite) precipitate at pH 4.5 to 5 and low Eh (approximately -0.1 V) as a consequence of water-rock reaction. Injection of CO2 decreases pH to approximately 3.5 and increases Eh by approximately 0.1 V, yielding secondary mineralization of euhedral pyrite instead of iron oxyhydroxides. Carbonate minerals also dissolve and ultimately re-precipitate, as determined by experiments in the Madison Limestone, but pyrite will persist and iron oxyhydroxides will not recrystallize.
The Chicxulub crater - impact metamorphism of sulfate and carbonate lithologies

NASA Astrophysics Data System (ADS)

Deutsch, A.; Langenhorst, F.; Hornemann, U.; Ivanov, B. A.

2003-04-01

It is discussed whether in the aftermath of the Chicxulub event, impact-released CO_2 and SO_x have changed the Earth's climate, acting also as lethal thread for life. Undoubtedly, vaporization of carbonates and sulfates, which are major target lithologies at the Chicxulub impact site, occurred in the footprint of the projectile. What happened to these lithologies outside this very restricted zone was so far unconstrained. Petrologic observations on PEMEX and UNAM as well as on the CSDP cores allow to set up a general classification for shock-related pro-grade effects on sulfate and carbonate sedimentary rocks. Shock effects in lithic breccias are restricted to brecciation and formation of twins in calcite. Suevites mostly lack melted carbonate clasts; annealing effects in anhydrite fragments are absent. The underlying melt breccias contain anhydrite fragments still displaying a sedimentary texture, and limestone clasts, whose texture reflect crystallization from melt. Impact melt breccias from deeper levels frequently contain partially resorbed anhydrite clasts and a melt matrix with the Ca-rich mineral assemblage quartz + plagioclase + clinopyroxene; this mineral assemblage provides evidence for partial dissociation of CaSO_4. Large clasts of anhydrite consist of equant crystals with 120^o triple junctions, a feature indicative for re-crystallization in the solid state. Tagamites (impact melt rocks) are virtually free of clasts from sedimentary lithologies. These rocks have an extremely high formation temperature, which caused total dissociation of CaSO_4 and CaCO_3. Finally, up to 100 μm wide veins of anhydrite + calcite + quartz cut the matrix of all lithologies except the tagamites. They probably represent "degassing vents". The given scheme is in qualitative accordance with data of shock recovery and annealing experiments as well as with modeling results. In addition, it substantiates that annealing plays a fundamental role in the impact metamorphism of sedimentary rocks.
Dielectric properties of water under extreme conditions and transport of carbonates in the deep Earth.

PubMed

Pan, Ding; Spanu, Leonardo; Harrison, Brandon; Sverjensky, Dimitri A; Galli, Giulia

2013-04-23

Water is a major component of fluids in the Earth's mantle, where its properties are substantially different from those at ambient conditions. At the pressures and temperatures of the mantle, experiments on aqueous fluids are challenging, and several fundamental properties of water are poorly known; e.g., its dielectric constant has not been measured. This lack of knowledge of water dielectric properties greatly limits our ability to model water-rock interactions and, in general, our understanding of aqueous fluids below the Earth's crust. Using ab initio molecular dynamics, we computed the dielectric constant of water under the conditions of the Earth's upper mantle, and we predicted the solubility products of carbonate minerals. We found that MgCO3 (magnesite)--insoluble in water under ambient conditions--becomes at least slightly soluble at the bottom of the upper mantle, suggesting that water may transport significant quantities of oxidized carbon. Our results suggest that aqueous carbonates could leave the subducting lithosphere during dehydration reactions and could be injected into the overlying lithosphere. The Earth's deep carbon could possibly be recycled through aqueous transport on a large scale through subduction zones.
Permeability Changes in Reaction Induced Fracturing

NASA Astrophysics Data System (ADS)

Ulven, Ole Ivar; Malthe-Sørenssen, Anders; Kalia, Rajiv

2013-04-01

The process of fracture formation due to a volume increasing chemical reaction has been studied in a variety of different settings, e.g. weathering of dolerites by Røyne et al.[4], serpentinization and carbonation of peridotite by Rudge et al.[3] and replacement reactions in silica-poor igneous rocks by Jamtveit et al.[1]. It is generally assumed that fracture formation will increase the net permeability of the rock, and thus increase the reactant transport rate and subsequently the total reaction rate, as summarised by Kelemen et al.[2]. Røyne et al.[4] have shown that transport in fractures will have an effect on the fracture pattern formed. Understanding the feedback process between fracture formation and permeability changes is essential in assessing industrial scale CO2 sequestration in ultramafic rock, but little is seemingly known about how large the permeability change will be in reaction-induced fracturing under compression, and it remains an open question how sensitive a fracture pattern is to permeability changes. In this work, we study the permeability of fractures formed under compression, and we use a 2D discrete element model to study the fracture patterns and total reaction rates achieved with different permeabilities. We achieve an improved understanding of the feedback processes in reaction-driven fracturing, thus improving our ability to decide whether industrial scale CO2 sequestration in ultramafic rock is a viable option for long-term handling of CO2. References [1] Jamtveit, B, Putnis, C. V., and Malthe-Sørenssen, A., "Reaction induced fracturing during replacement processes," Contrib. Mineral Petrol. 157, 2009, pp. 127 - 133. [2] Kelemen, P., Matter, J., Streit, E. E., Rudge, J. F., Curry, W. B., and Blusztajn, J., "Rates and Mechanisms of Mineral Carbonation in Peridotite: Natural Processes and Recipes for Enhanced, in situ CO2 Capture and Storage," Annu. Rev. Earth Planet. Sci. 2011. 39:545-76. [3] Rudge, J. F., Kelemen, P. B., and Spiegelman, M., "A simple model of reaction induced cracking applied to serpentinization and carbonation of peridotite," Earth Planet. Sci. Lett. 291, Issues 1-4, 2010, pp. 215 - 227. [4] Røyne, A., Jamtveit, B., and Malthe-Sørenssen, A., "Controls on rock weathering rates by reaction-induced hierarchial fracturing," Earth Planet. Sci. Lett. 275, 2008, pp. 364 - 369.

Fractures in Carbonate-Bearing Rocks at Mars Huygens Basin

NASA Image and Video Library

2011-03-08

This false-color image NASA Mars Reconnaissance Orbiter shows that fractures and possible layers are visible in the light-toned rock exposure containing the carbonates. The location is inside an unnamed crater on the uplifted rim of Huygens crater.
Textural and isotopic evidence for Ca-Mg carbonate pedogenesis

NASA Astrophysics Data System (ADS)

Diaz-Hernandez, J. L.; Sánchez-Navas, A.; Delgado, A.; Yepes, J.; Garcia-Casco, A.

2018-02-01

Models for evaluating the terrestrial carbon cycle must take into account not only soil organic carbon, represented by a mixture of plant and animal remains, but also soil inorganic carbon, contained in minerals, mainly in calcite and dolomite. Thick soil caliches derived from weathering of mafic and ultramafic rocks must be considered as sinks for carbon storage in soils. The formation of calcite and dolomite from pedogenic alteration of volcanic tephras under an aridic moisture regime is studied in an unusually thick 3-m soil profile on Gran Canaria island (Canary Islands, Spain). The biological activity of the pedogenic environment (soil respiration) releases CO2 incorporated as dissolved inorganic carbon (DIC) in waters. It drives the formation of low-magnesian calcite and calcian dolomite over basaltic substrates, with a δ13C negative signature (-8 to -6‰ vs. V-PDB). Precipitation of authigenic carbonates in the soil is accompanied by the formation of Mg-rich clay minerals and quartz after the weathering of basalts. Mineralogical, textural, compositional, and isotopic variations throughout the soil profile studied indicate that dolomite formed at greater depths and earlier than the calcite. The isotopic signatures of the surficial calcite and deeper dolomite crusts are primary and resulted from the dissolution-precipitation cycles that led to the formation of both types of caliches under different physicochemical conditions. Dolomite formed within a clay-rich matrix through diffusive transport of reactants. It is precipitated from water with more negative δ18O values (-1.5 to -3.5‰ vs. V-SMOW) in the subsoil compared to those of water in equilibrium with surficial calcite. Thus, calcite precipitated after dolomite, and directly from percolating solutions in equilibrium with vadose water enriched in δ18O (-0.5 to +1.5‰) due to the evaporation processes. The accumulation of inorganic carbon reaches 586.1 kg m-2 in the soil studied, which means that the carbon sequestration capacity of mafic rocks must be taken into account for certain terrestrial settings. Dolomite together with calcite should be assessed when quantifying carbon stored in arid-semiarid soils as a result of the natural weathering processes.
Mineral displacement and -dissolution processes and their relevance to rock porosity and permeability in Rotliegend sandstones of the Altmark natural gas field (central Germany) - results from CO2 laboratory batch experiments

NASA Astrophysics Data System (ADS)

Pudlo, Dieter; Enzmann, Frieder; Heister, Katja; Werner, Lars; Ganzer, Leonhard; Reitenbach, Viktor; Henkel, Steven; Albrecht, Daniel; Gaupp, Reinhard

2014-05-01

The Rotliegend reservoir sandstones of the Altmark area (central Germany) comprise the second largest natural gas field of Europe. These sandstones were deposited on a playa-like continental platform with braided river systems, ephemeral lakes and aeolian dunes under semi-arid conditions. Some of the pristine, red coloured deposits suffered intensive late diagenetic alteration and are now preserved as bleached, high porous and permeable sandstones. To evaluate the relevance of distinct fluids and their fluid-rock alteration reactions on such bleaching processes we performed laboratory static batch experiments on the Altmark sandstones. These 4-6 week lasting runs were conducted with CO2 saturated synthetic brines under typical Altmark reservoir conditions (p= 20 MPa, T= 125°C). Thereby mineralogical, petrophysical and (hydro- and geo-) chemical rock features were maintained prior and after the experiments. Chemical data proved the dissolution of carbonate and sulphate minerals during the runs, whereas the variation in abundance of further elements was within the detection limit of analytical accuracy. However, FE-SEM investigations on used, evaporated brines reveal the presence of illite and chlorite minerals within a matrix of Ca-, Si-, Fe, Al-, Na- and S components (carbonate, anhydrite, albite and Fe-(hydr-) oxides ?). By porosity and relative permeability measurements an increase in both rock features was observed after the runs, indicating that mineral dissolution and/or (clay) fine migration/detachment occurred during the experiments. Mineral dissolution, especially of pore-filling cements (e.g. carbonate-, sulphate minerals) is also deduced by BET analysis, in determining the specific surface of the sandstones. The size of these reactive surfaces increased after the experiments, suggesting that after the dissolution of pore-filling cements, formerly armoured grain rimming clay cutans were exposed to potential migrating fluids. These findings are also supported by µ-CT investigations. Here, the achieved 3D modelling data indicate an increase in reactive surface areas exposed to the pore space (which is in accord to the BET observations), as well as an enhancement in rock porosity and permeability after the runs. Moreover, these simulations showed that a remarkable mass (mineral) transfer was induced by the experiments, which led to a displacement of the porosity and permeability distribution in the sandstones and therefore a change in the fluid flow characteristics within the rocks - a parameter most important for every fluid-rock process. These observations are quite astonishing because they suggest that not only fluid velocity (e.g. during fluid flow experiments) might detach and transport grain rimming (clay) minerals, but also that physico-chemical reactions may enforce the release of such solids, even during almost static p-/T-/Xfluid conditions, as used in our experiments.
[Biogeochemical processes of the major ions and dissolved inorganic carbon in the Guijiang River].

PubMed

Tang, Wen-Kui; Tao, Zhen; Gao, Quan-Zhou; Mao, Hai-Ruo; Jiang, Guang-Hui; Jiao, Shu-Lin; Zheng, Xiong-Bo; Zhang, Qian-Zhu; Ma, Zan-Wen

2014-06-01

Within the drainage basin, information about natural processes and human activities can be recorded in the chemical composition of riverine water. The analysis of the Guijiang River, the first level tributary of the Xijiang River, demonstrated that the chemical composition of water in the Guijiang River was mainly influenced by the chemical weathering of carbonate rocks within the drainage basin, in which CO2 was the main erosion medium, and that the weathering of carbonate rock by H2SO4 had a remarkable impact on the water chemical composition in the Guijiang River. Precipitation, human activities, the weathering of carbonate rocks and silicate rocks accounted for 2.7%, 6.3%, 72.8% and 18.2% of the total dissolved load, respectively. The stable isotopic compositions of dissolved inorganic carbon (delta13C(DIC)) indicated that DIC in the Guijiang River had been assimilated by the phytoplankton in photosynthesis. The primary production of phytoplankton contributed to 22.3%-30.9% of particulate organic carbon (POC) in the Guijiang River, which implies that phytoplankton can transform DIC into POC by photosynthesis, and parts of POC will sink into the bottom of the river in transit, which leads into the formation of burial organic carbon.
Transport of Organic Contaminants Mobilized from Coal through Sandstone Overlying a Geological Carbon Sequestration Reservoir

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zhong, Lirong; Cantrell, Kirk J.; Bacon, Diana H.

2014-02-01

Column experiments were conducted using a wetted sandstone rock installed in a tri-axial core holder to study the flow and transport of organic compounds mobilized by scCO2 under simulated geologic carbon storage (GCS) conditions. The sandstone rock was collected from a formation overlying a deep saline reservoir at a GCS demonstration site. Rock core effluent pressures were set at 0, 500, or 1000 psig and the core temperature was set at 20 or 50°C to simulate the transport to different subsurface depths. The concentrations of the organic compounds in the column effluent and their distribution within the sandstone core weremore » monitored. Results indicate that the mobility though the core sample was much higher for BTEX compounds than for naphthalene. Retention of organic compounds from the vapor phase to the core appeared to be primarily controlled by partitioning from the vapor phase to the aqueous phase. Adsorption to the surfaces of the wetted sandstone was also significant for naphthalene. Reduced temperature and elevated pressure resulted in greater partitioning of the mobilized organic contaminants into the water phase.« less
Evidence for Late-Paleozoic brine migration in Cambrian carbonate rocks of the central and southern Appalachians: Implications for Mississippi Valley-type sulfide mineralization

USGS Publications Warehouse

Hearn, P.P.; Sutter, J.F.; Belkin, H.E.

1987-01-01

Many Lower Paleozoic limestones and dolostones in the Valley and Ridge province of the central and southern Appalachians contain 10 to 25 weight percent authigenic potassium feldspar. This was considered to be a product of early diagenesis, however, 40Ar 39Ar analyses of overgrowths on detrital K-feldspar in Cambrian carbonate rocks from Pennsylvania, Maryland, Virginia, and Tennessee yield Late Carboniferous-Early Permian ages (278-322 Ma). Simple mass balance calculations suggest that the feldspar could not have formed isochemically, but required the flux of multiple pore volumes of fluid through the rocks, reflecting regional fluid migration events during the Late-Paleozoic Alleghanian orogeny. Microthermometric measurements of fluid inclusions in overgrowths on detrital K-feldspar and quartz grains from unmineralized rocks throughout the study area indicate homogenization temperatures from 100?? to 200??C and freezing point depressions of -14?? to -18.5??C (18-21 wt.% NaCl equiv). The apparent similarity of these fluids to fluid inclusions in ore and gangue minerals of nearby Mississippi Valley-type (MVT) deposits suggests that the regional occurrences of authigenic K-feldspar and MVT mineralization may be genetically related. This hypothesis is supported by the discovery of authigenic K-feldspar intergrown with sphalerite in several mines of the Mascot-Jefferson City District, E. Tennessee. Regional potassic alteration in unmineralized carbonate rocks and localized occurrences of MVT mineralization are both explainable by a gravity-driven flow model, in which deep brines migrate towards the basin margin under a hydraulic gradient established during the Alleghanian orogeny. The authigenic K-feldspar may reflect the loss of K during disequilibrium cooling of the ascending brines. MVT deposits are probably localized manifestations of the same migrating fluids, occurring where the necessary physical and chemical traps are present. ?? 1987.
Geochemical behavior of ultramafic waste rocks with carbon sequestration potential: a case study of the Dumont Nickel Project, Amos, Québec.

PubMed

Kandji, El Hadji Babacar; Plante, Benoit; Bussière, Bruno; Beaudoin, Georges; Dupont, Pierre-Philippe

2017-04-01

The geochemical behavior of ultramafic waste rocks and the effect of carbon sequestration by these waste rocks on the water drainage quality were investigated using laboratory-scale kinetic column tests on samples from the Dumont Nickel Project (RNC Minerals, QC, Canada). The test results demonstrated that atmospheric CO 2 dissolution induced the weathering of serpentine and brucite within the ultramafic rocks, generating high concentrations of Mg and HCO 3 - with pH values ranging between 9 and 10 in the leachates that promote the precipitation of secondary Mg carbonates. These alkaline pH values appear to have prevented the mobilization of many metals; Fe, Ni, Cu, and Zn were found at negligible concentrations in the leachates. Posttesting characterization using chemical analyses, diffuse reflectance infrared Fourier transform (DRIFT), and scanning electron microscope (SEM) observations confirmed the precipitation of secondary hydrated Mg carbonates as predicted by thermodynamic calculations. The formation of secondary Mg carbonates induced cementation of the waste particles, resulting in the development of a hardpan.
The Martian ocean: First acid, then alkaline

NASA Technical Reports Server (NTRS)

Schaefer, M. W.

1992-01-01

In Mars' distant past, carbon dioxide and water may have been plentiful. Values of total outgassed CO2 from several to about 10 bar are consistent with present knowledge, and this amount of CO2 implies an amount of water outgassed equal to an equivalent depth of 500 to 1000 m. It is quite reasonable, therefore, to envision an early Mars in which there was a body or bodies of liquid water, perhaps in the northern plains, and a dense carbon dioxide atmosphere. Under such conditions, the pH of the water will be low, due to the dissolution of carbon dioxide in the water to form carbonic acid. This acidic water is capable of weathering the available rock quite intensely, particularly because this rock is likely to be heavily fractured (from meteorite bombardment) or even consist of fine particles (such as pyroclastic deposits). As time goes on, however, the carbon dioxide atmosphere will rapidly pass through the ocean to form carbonate deposits. As the density of the atmosphere decreases, so will the flux of carbonic acid into the ocean. Without this input of carbonic acid, the effect of the dissolved weathering products will be to increase the pH of the water. The ocean will then become alkaline. To study this process, I have developed a geochemical cycle model for the atmosphere-hydrosphere-regolith system of Mars. The treatment of geochemical cycles as complex kinetic chemical reactions has been undertaken for terrestrial systems in recent years with much success. This method is capable of elegantly handling the interactions between the simultaneous chemical reactions needed to understand such a system.
Sediment-hosted micro-disseminated gold mineralization constrained by basin paleo-topographic highs in the Youjiang basin, South China

NASA Astrophysics Data System (ADS)

Liu, Jianming; Ye, Jie; Ying, Hanlong; Liu, Jiajun; Zheng, Minghua; Gu, Xuexiang

2002-06-01

The Youjiang basin is a Devonian-Triassic rift basin on the southern margin of the Yangtze Craton in South China. Strong syndepositional faulting defined the basin-and-range style paleo-topography that further developed into isolated carbonate platforms surrounded by siliciclastic filled depressions. Finally, thick Triassic siliciclastic deposits covered the platforms completely. In the Youjiang basin, numerous sediment-hosted, micro-disseminated gold (SMG) deposits occur mainly in Permian-Triassic chert and siliciclastic rocks. SMG ores are often auriferous sedimentary rocks with relatively low sulfide contents and moderate to weak alteration. Similar to Carlin-type gold ores in North America, SMG ores in the Youjiang basin are characterized by low-temperature mineral assemblages of pyrite, arsenopyrite, realgar, stibnite, cinnabar, marcasite, chalcedony and carbonate. Most of the SMG deposits are remarkably distributed around the carbonate platforms. Accordingly, there are platform-proximal and platform-distal SMG deposits. Platform-proximal SMG deposits often occur in the facies transition zone between the underlying platform carbonate rocks and the overlying siliciclastic rocks with an unconformity (often a paleo-karst surface) in between. In the ores and hostrocks there are abundant synsedimentary-syndiagenetic fabrics such as lamination, convolute bedding, slump texture, soft-sediment deformation etc. indicating submarine hydrothermal deposition and syndepositional faulting. Numerous fluid-escape and liquefaction fabrics imply strong fluid migration during sediment basin evolution. Such large-scale geological and fabric evidence implies that SMG ores were formed during basin evolution, probably in connection with basinal fluids. It is well known that basinal fluids (especially sediment-sourced fluids) will migrate generally (1) upwards, (2) towards basin margins or basin topographic highs, (3) and from thicker towards thinner deposits during basin evolution. The isolated carbonate platform (as a basin paleo-high) and related syndepositional fault system, together with the unconformity-related facies succession, may have controlled the migration pathway of ore-forming basinal fluids and subsequently determined the location of SMG deposits in the Youjiang basin. Unlike Carlin-type gold deposits, SMG mineralization in the Youjiang basin may represent an integral aspect of the dynamic evolution of extensional basins along divergent continental margins.
Clastic dikes of Heart Mountain fault breccia, northwestern Wyoming, and their significance

USGS Publications Warehouse

Pierce, W.G.

1979-01-01

Structural features in northwestern Wyoming indicate that the Heart Mountain fault movement was an extremely rapid, cataclysmic event that created a large volume of carbonate fault breccia derived entirely from the lower part of the upper plate. After fault movement had ceased, much of the carbonate fault breccia, here called calcibreccia, lay loose on the resulting surface of tectonic denudation. Before this unconsolidated calcibreccia could be removed by erosion, it was buried beneath a cover of Tertiary volcanic rocks: the Wapiti Formation, composed of volcanic breccia, poorly sorted volcanic breccia mudflows, and lava flows, and clearly shown in many places by inter lensing and intermixing of the calcibreccia with basal volcanic rocks. As the weight of volcanic overburden increased, the unstable water-saturated calcibreccia became mobile and semifluid and was injected upward as dikes into the overlying volcanic rocks and to a lesser extent into rocks of the upper plate. In some places the lowermost part of the volcanic overburden appears to have flowed with the calcibreccia to form dike like bodies of mixed volcanic rock and calcibreccia. One calcibreccia dike even contains carbonized wood, presumably incorporated into unconsolidated calcibreccia on the surface of tectonic denudation and covered by volcanic rocks before moving upward with the dike. Angular xenoliths of Precambrian rocks, enclosed in another calcibreccia dike and in an adjoining dikelike mass of volcanic rock as well, are believed to have been torn from the walls of a vent and incorporated into the basal part of the Wapiti Formation overlying the clastic carbonate rock on the fault surface. Subsequently, some of these xenoliths were incorporated into the calcibreccia during the process of dike intrusion. Throughout the Heart Mountain fault area, the basal part of the upper-plate blocks or masses are brecciated, irrespective of the size of the blocks, more intensely at the base and in places extending upward for several tens of meters. North of Republic Mountain a small 25-m-high upper-plate mass, brecciated to some degree throughout, apparently moved some distance along the Heart Mountain fault as brecciated rock. Calcibreccia dikes intrude upward from the underlying 2 m of fault breccia into the lower part of the mass and also from its top into the overlying volcanic rocks; an earthquake-related mechanism most likely accounts for the observed features of this deformed body. Calcibreccia dikes are more common within the bedding-plane phase of the Heart Mountain fault but also occur in its transgressive and former land-surface phases. Evidence that the Wapiti Formation almost immediately buried loose, unconsolidated fault breccia that was the source of the dike rock strongly suggests a rapid volcanic deposition over the area in which clastic dikes occur, which is at least 75 km long. Clastic dikes were injected into both the upper-plate and the volcanic rocks at about the same time, after movement on the Heart Mouuntain fault had ceased, and therefore do not indicate a fluid-flotation mechanism for the Heart Mountain fault. The difference between contacts of the clastic dikes with both indurated and unconsolidated country rock is useful in field mapping at localities where it is difficult to distinguish between volcanic rocks of the Cathedral Cliffs and Lamar River Formations, and the Wapiti Formation. Thus, calcibreccia dikes in the Cathedral Cliffs and Lamar River Formations show a sharp contact because the country rock solidified prior to fault movement, whereas calcibreccia dikes in the Wapiti Formation in many instances show a transitional or semifluid contact because the country rock was still unconsolidated or semifluid at the time of dike injection.
Carbon Compounds from Mars Found Inside Meteorite ALH84001

NASA Image and Video Library

1996-08-08

This 4.5 billion-year-old rock, labeled meteorite ALH84001, is one of 10 rocks from Mars in which researchers have found organic carbon compounds that originated on Mars without involvement of life. http://photojournal.jpl.nasa.gov/catalog/PIA00289
Some open issues in the analysis of the storage and migration properties of fractured carbonate reservoirs

NASA Astrophysics Data System (ADS)

Agosta, Fabrizio

2017-04-01

Underground CO2 storage in depleted hydrocarbon reservoirs may become a common practice in the future to lower the concentration of greenhouse gases in the atmosphere. Results from the first experiments conducted in carbonate rocks, for instance the Lacq integrated CCS Pilot site, SW France, are quite exciting. All monitored parameters, such as the CO2 concentration at well sites, well pressures, cap rock integrity and environmental indicators show the long-term integrity of this type of geological reservoirs. Other positive news arise from the OXY-CFB-300 Compostilla Project, NW Spain, where most of the injected CO2 dissolved into the formation brines, suggesting the long-term security of this method. However, in both cases, the CO2- rich fluids partially dissolved the carbonate minerals during their migration through the fractured reservoir, modifying the overall pore volume and pressure regimes. These results support the growing need for a better understanding of the mechanical behavior of carbonate rocks over geological time of scales. In fact, it is well known that carbonates exhibit a variety of deformation mechanisms depending upon many intrinsic factors such as composition, texture, connected pore volume, and nature of the primary heterogeneities. Commonly, tight carbonates are prone to opening-mode and/or pressure solution deformation. The interplay between these two mechanisms likely affects the petrophysical properties of the fault damage zones, which form potential sites for CO2 storage due to their high values of both connected porosity and permeability. On the contrary, cataclastic deformation produces fault rocks that often form localized fluid barriers for cross-fault fluid flow. Nowadays, questions on the conditions of sealing/leakage of carbonate fault rocks are still open. In particular, the relative role played by bulk crushing, chipping, cementation, and pressure solution on connected porosity of carbonate fault rocks during structural evolution and diagenesis is not determined yet. Differently, porous rocks are mainly affected by deformation banding. The latter process involves the collapse of primary porosity within narrow bands, which often localize into well-developed clusters. Currently, researchers focus on the assessment of the 3D pore geometry of the shear bands, which may act as possible sites for residual C02 trapping. The fault-bounded rock volumes are mainly crosscut by background fractures. These diffuse fractures are often compartmentalized into discrete mechanical units, which are bounded by primary heterogeneities such as bed interfaces and transgressive erosional surfaces. Moreover, bed-parallel pressure solution seams, structural elements that commonly form in limestone rocks during burial diagenesis, can also act as mechanical interfaces during growth of background fractures. However, early embrittlement of carbonates was also documented, suggesting to further investigate their diagenetic evolution to determine the conditions at which the latter phenomenon takes place. Results could shed new lights into the storage properties and, hence, the amount of CO2 that can be securely stored within significant volumes of fractured carbonates in the underground.
Temperature and composition of carbonate cements record early structural control on cementation in a nascent deformation band fault zone: Moab Fault, Utah, USA

NASA Astrophysics Data System (ADS)

Hodson, Keith R.; Crider, Juliet G.; Huntington, Katharine W.

2016-10-01

Fluid-driven cementation and diagenesis within fault zones can influence host rock permeability and rheology, affecting subsequent fluid migration and rock strength. However, there are few constraints on the feedbacks between diagenetic conditions and structural deformation. We investigate the cementation history of a fault-intersection zone on the Moab Fault, a well-studied fault system within the exhumed reservoir rocks of the Paradox Basin, Utah, USA. The fault zone hosts brittle structures recording different stages of deformation, including joints and two types of deformation bands. Using stable isotopes of carbon and oxygen, clumped isotope thermometry, and cathodoluminescence, we identify distinct source fluid compositions for the carbonate cements within the fault damage zone. Each source fluid is associated with different carbonate precipitation temperatures, luminescence characteristics, and styles of structural deformation. Luminescent carbonates appear to be derived from meteoric waters mixing with an organic-rich or magmatic carbon source. These cements have warm precipitation temperatures and are closely associated with jointing, capitalizing on increases in permeability associated with fracturing during faulting and subsequent exhumation. Earlier-formed non-luminescent carbonates have source fluid compositions similar to marine waters, low precipitation temperatures, and are closely associated with deformation bands. The deformation bands formed at shallow depths very early in the burial history, preconditioning the rock for fracturing and associated increases in permeability. Carbonate clumped isotope temperatures allow us to associate structural and diagenetic features with burial history, revealing that structural controls on fluid distribution are established early in the evolution of the host rock and fault zone, before the onset of major displacement.
Field and petrological study of metasomatism and high-pressure carbonation from lawsonite eclogite-facies terrains, Alpine Corsica

NASA Astrophysics Data System (ADS)

Piccoli, Francesca; Vitale Brovarone, Alberto; Ague, Jay J.

2018-04-01

This study presents new field and petrological data on carbonated metasomatic rocks from the lawsonite-eclogite units of Alpine Corsica. These rocks form along major, slab-scale lithological boundaries of the subducted Alpine Tethys plate. Our results indicate that a large variety of rocks ranging from metamafic/ultramafic to metafelsic can react with carbon-bearing fluids, leading to carbon sequestration at high-pressure conditions. The process of carbonation includes both replacement of silicates by high-pressure carbonate, and carbonate veining. The field, microstructural and mineralogical data strongly suggest that the metasomatism was mediated by the infiltration of external fluids of mixed origin, including both mafic/ultramafic and metasedimentary sources. Our results support the following three-step evolution: (i) Release of aqueous fluids by lawsonite and/or antigorite breakdown at depth; (ii) Fluid channelization along the base of the metasedimentary pile of the subducted lithospheric plate and related reactive fluid flow leading to carbonate mineral dissolution; (iii) Further interactions of the resulting carbon-bearing fluids with slab-forming rocks at depths of ca. 70 km and carbonation of pre-existing silicate-rich lithologies. This study highlights the importance of carbonate-bearing fluids evolving along down-T, down-P paths, such as along slab-parallel lithological boundaries, for the sequestration of carbon in subduction zones, and suggests that similar processes may also operate in collisional settings. Fig. S2: Petrogenetic grid in the CaFMASH+CO2 system for the antigorite and clinopyroxene carbonation reactions, together with grossular forming reaction during decarbonation. Reactions are written with the high T assemblage to the right of the = sign.
Mechanical Behavior of Low Porosity Carbonate Rock: From Brittle Creep to Ductile Creep.

NASA Astrophysics Data System (ADS)

Nicolas, A.; Fortin, J.; Gueguen, Y.

2014-12-01

Mechanical compaction and associated porosity reduction play an important role in the diagenesis of porous rocks. They may also affect reservoir rocks during hydrocarbon production, as the pore pressure field is modified. This inelastic compaction can lead to subsidence, cause casing failure, trigger earthquake, or change the fluid transport properties. In addition, inelastic deformation can be time - dependent. In particular, brittle creep phenomena have been deeply investigated since the 90s, especially in sandstones. However knowledge of carbonates behavior is still insufficient. In this study, we focus on the mechanical behavior of a 14.7% porosity white Tavel (France) carbonate rock (>98% calcite). The samples were deformed in a triaxial cell at effective confining pressures ranging from 0 MPa to 85 MPa at room temperature and 70°C. Experiments were carried under dry and water saturated conditions in order to explore the role played by the pore fluids. Two types of experiments have been carried out: (1) a first series in order to investigate the rupture envelopes, and (2) a second series with creep experiments. During the experiments, elastic wave velocities (P and S) were measured to infer crack density evolution. Permeability was also measured during creep experiments. Our results show two different mechanical behaviors: (1) brittle behavior is observed at low confining pressures, whereas (2) ductile behavior is observed at higher confining pressures. During creep experiments, these two behaviors have a different signature in term of elastic wave velocities and permeability changes, due to two different mechanisms: development of micro-cracks at low confining pressures and competition between cracks and microplasticity at high confining pressure. The attached figure is a summary of 20 triaxial experiments performed on Tavel limestone under different conditions. Stress states C',C* and C*' and brittle strength are shown in the P-Q space: (a) 20°C and dry, (b) 20°C and water saturated samples, (c) 70°C dry and (d) summary of all the experiments. Three regimes of inelastic and failure modes are observed: brittle failure, shear-enhanced compaction and dilatant cataclastic flow.
Prediction of carbonate rock type from NMR responses using data mining techniques

NASA Astrophysics Data System (ADS)

Gonçalves, Eduardo Corrêa; da Silva, Pablo Nascimento; Silveira, Carla Semiramis; Carneiro, Giovanna; Domingues, Ana Beatriz; Moss, Adam; Pritchard, Tim; Plastino, Alexandre; Azeredo, Rodrigo Bagueira de Vasconcellos

2017-05-01

Recent studies have indicated that the accurate identification of carbonate rock types in a reservoir can be employed as a preliminary step to enhance the effectiveness of petrophysical property modeling. Furthermore, rock typing activity has been shown to be of key importance in several steps of formation evaluation, such as the study of sedimentary series, reservoir zonation and well-to-well correlation. In this paper, a methodology based exclusively on the analysis of 1H-NMR (Nuclear Magnetic Resonance) relaxation responses - using data mining algorithms - is evaluated to perform the automatic classification of carbonate samples according to their rock type. We analyze the effectiveness of six different classification algorithms (k-NN, Naïve Bayes, C4.5, Random Forest, SMO and Multilayer Perceptron) and two data preprocessing strategies (discretization and feature selection). The dataset used in this evaluation is formed by 78 1H-NMR T2 distributions of fully brine-saturated rock samples from six different rock type classes. The experiments reveal that the combination of preprocessing strategies with classification algorithms is able to achieve a prediction accuracy of 97.4%.
Carbonate precipitation under bulk acidic conditions as a potential biosignature for searching life on Mars

NASA Astrophysics Data System (ADS)

Fernández-Remolar, David C.; Preston, Louisa J.; Sánchez-Román, Mónica; Izawa, Matthew R. M.; Huang, L.; Southam, Gordon; Banerjee, Neil R.; Osinski, Gordon R.; Flemming, Roberta; Gómez-Ortíz, David; Prieto Ballesteros, Olga; Rodríguez, Nuria; Amils, Ricardo; Darby Dyar, M.

2012-10-01

Recent observations of carbonate minerals in ancient Martian rocks have been interpreted as evidence for the former presence of circumneutral solutions optimal for carbonate precipitation. Sampling from surface and subsurface regions of the low-pH system of Río Tinto has shown, unexpectedly, that carbonates can form under diverse macroscopic physicochemical conditions ranging from very low to neutral pH (1.5-7.0). A multi-technique approach demonstrates that carbonate minerals are closely associated with microbial activity. Carbonates occur in the form of micron-size carbonate precipitates under bacterial biofilms, mineralization of subsurface colonies, and possible biogenic microstructures including globules, platelets and dumbbell morphologies. We propose that carbonate precipitation in the low-pH environment of Río Tinto is a process enabled by microbially-mediated neutralization driven by the reduction of ferric iron coupled to the oxidation of biomolecules in microbially-maintained circumneutral oases, where the local pH (at the scale of cells or cell colonies) can be much different than in the macroscopic environment. Acidic conditions were likely predominant in vast regions of Mars over the last four billion years of planetary evolution. Ancient Martian microbial life inhabiting low-pH environments could have precipitated carbonates similar to those observed at Río Tinto. Preservation of carbonates at Río Tinto over geologically significant timescales suggests that similarly-formed carbonate minerals could also be preserved on Mars. Such carbonates could soon be observed by the Mars Science Laboratory, and by future missions to the red planet.
Application of geologic map information to water quality issues in the southern part of the Chesapeake Bay watershed, Maryland and Virginia, eastern United States

USGS Publications Warehouse

McCartan, L.; Peper, J.D.; Bachman, L.J.; Horton, J. Wright

1999-01-01

Geologic map units contain much information about the mineralogy, chemistry, and physical attributes of the rocks mapped. This paper presents information from regional-scale geologic maps in Maryland and Virginia, which are in the southern part of the Chesapeake Bay watershed in the eastern United States. The geologic map information is discussed and analyzed in relation to water chemistry data from shallow wells and stream reaches in the area. Two environmental problems in the Chesapeake Bay watershed are used as test examples. The problems, high acidity and high nitrate concentrations in streams and rivers, tend to be mitigated by some rock and sediment types and not by others. Carbonate rocks (limestone, dolomite, and carbonate-cemented rocks) have the greatest capacity to neutralize acidic ground water and surface water in contact with them. Rocks and sediments having high carbon or sulfur contents (such as peat and black shale) potentially contribute the most toward denitrification of ground water and surface water in contact with them. Rocks and sediments that are composed mostly of quartz, feldspar, and light-colored clay (rocks such as granite and sandstone, sediments such as sand and gravel) tend not to alter the chemistry of waters that are in contact with them. The testing of relationships between regionally mapped geologic units and water chemistry is in a preliminary stage, and initial results are encouraging.Geologic map units contain much information about the mineralogy, chemistry, and physical attributes of the rocks mapped. This paper presents information from regional-scale geologic maps in Maryland and Virginia, which are in the southern part of the Chesapeake Bay watershed in the eastern United States. The geologic map information is discussed and analyzed in relation to water chemistry data from shallow wells and stream reaches in the area. Two environmental problems in the Chesapeake Bay watershed are used as test examples. The problems, high acidity and high nitrate concentrations in streams and rivers, tend to be mitigated by some rock and sediment types and not by others. Carbonate rocks (limestone, dolomite, and carbonate-cemented rocks) have the greatest capacity to neutralize acidic ground water and surface water in contact with them. Rocks and sediments having high carbon or sulfur contents (such as peat and black shale) potentially contribute the most toward denitrification of ground water and surface water in contact with them. Rocks and sediments that are composed mostly of quartz, feldspar, and light-colored clay (rocks such as granite and sandstone, sediments such as sand and gravel) tend not to alter the chemistry of waters that are in contact with them. The testing of relationships between regionally mapped geologic units and water chemistry is in a preliminary stage, and initial results are encouraging.
Dissolution and secondary mineral precipitation in basalts due to reactions with carbonic acid

NASA Astrophysics Data System (ADS)

Kanakiya, Shreya; Adam, Ludmila; Esteban, Lionel; Rowe, Michael C.; Shane, Phil

2017-06-01

One of the leading hydrothermal alteration processes in volcanic environments is when rock-forming minerals with high concentrations of iron, magnesium, and calcium react with CO2 and water to form carbonate minerals. This is used to the advantage of geologic sequestration of anthropogenic CO2. Here we experimentally investigate how mineral carbonation processes alter the rock microstructure due to CO2-water-rock interactions. In order to characterize these changes, CO2-water-rock alteration in Auckland Volcanic Field young basalts (less than 0.3 Ma) is studied before and after a 140 day reaction period. We investigate how whole core basalts with similar geochemistry but different porosity, permeability, pore geometry, and volcanic glass content alter due to CO2-water-rock reactions. Ankerite and aluminosilicate minerals precipitate as secondary phases in the pore space. However, rock dissolution mechanisms are found to dominate this secondary mineral precipitation resulting in an increase in porosity and decrease in rigidity of all samples. The basalt with the highest initial porosity and volcanic glass volume shows the most secondary mineral precipitation. At the same time, this sample exhibits the greatest increase in porosity and permeability, and a decrease in rock rigidity post reaction. For the measured samples, we observe a correlation between volcanic glass volume and rock porosity increase due to rock-fluid reactions. We believe this study can help understand the dynamic rock-fluid interactions when monitoring field scale CO2 sequestration projects in basalts.
Simulation of Ground-Water Flow in the Shenandoah Valley, Virginia and West Virginia, Using Variable-Direction Anisotropy in Hydraulic Conductivity to Represent Bedrock Structure

USGS Publications Warehouse

Yager, Richard M.; Southworth, Scott C.; Voss, Clifford I.

2008-01-01

Ground-water flow was simulated using variable-direction anisotropy in hydraulic conductivity to represent the folded, fractured sedimentary rocks that underlie the Shenandoah Valley in Virginia and West Virginia. The anisotropy is a consequence of the orientations of fractures that provide preferential flow paths through the rock, such that the direction of maximum hydraulic conductivity is oriented within bedding planes, which generally strike N30 deg E; the direction of minimum hydraulic conductivity is perpendicular to the bedding. The finite-element model SUTRA was used to specify variable directions of the hydraulic-conductivity tensor in order to represent changes in the strike and dip of the bedding throughout the valley. The folded rocks in the valley are collectively referred to as the Massanutten synclinorium, which contains about a 5-km thick section of clastic and carbonate rocks. For the model, the bedrock was divided into four units: a 300-m thick top unit with 10 equally spaced layers through which most ground water is assumed to flow, and three lower units each containing 5 layers of increasing thickness that correspond to the three major rock units in the valley: clastic, carbonate and metamorphic rocks. A separate zone in the carbonate rocks that is overlain by colluvial gravel - called the western-toe carbonate unit - was also distinguished. Hydraulic-conductivity values were estimated through model calibration for each of the four rock units, using data from 354 wells and 23 streamflow-gaging stations. Conductivity tensors for metamorphic and western-toe carbonate rocks were assumed to be isotropic, while conductivity tensors for carbonate and clastic rocks were assumed to be anisotropic. The directions of the conductivity tensor for carbonate and clastic rocks were interpolated for each mesh element from a stack of 'form surfaces' that provided a three-dimensional representation of bedrock structure. Model simulations were run with (1) variable strike and dip, in which conductivity tensors were aligned with the strike and dip of the bedding, and (2) uniform strike in which conductivity tensors were assumed to be horizontally isotropic with the maximum conductivity direction parallel to the N30 deg E axis of the valley and the minimum conductivity direction perpendicular to the horizontal plane. Simulated flow penetrated deeper into the aquifer system with the uniform-strike tensor than with the variable-strike-and-dip tensor. Sensitivity analyses suggest that additional information on recharge rates would increase confidence in the estimated parameter values. Two applications of the model were conducted - the first, to determine depth of recent ground-water flow by simulating the distribution of ground-water ages, showed that most shallow ground water is less than 10 years old. Ground-water age distributions computed by variable-strike-and-dip and uniform-strike models were similar, but differed beneath Massanutten Mountain in the center of the valley. The variable-strike-and-dip model simulated flow from west to east parallel to the bedding of the carbonate rocks beneath Massanutten Mountain, while the uniform-strike model, in which flow was largely controlled by topography, simulated this same area as an east-west ground-water divide. The second application, which delineated capture zones for selected well fields in the valley, showed that capture zones delineated with both models were similar in plan view, but differed in vertical extent. Capture zones simulated by the variable-strike-and-dip model extended downdip with the bedding of carbonate rock and were relatively shallow, while those simulated by the uniform-strike model extended to the bottom of the flow system, which is unrealistic. These results suggest that simulations of ground-water flow through folded fractured rock can be constructed using SUTRA to represent variable orientations of the hydraulic-conductivity tensor and produce a

Digital Rock Simulation of Flow in Carbonate Samples

NASA Astrophysics Data System (ADS)

Klemin, D.; Andersen, M.

2014-12-01

Reservoir engineering has becomes more complex to deal with current challenges, so core analysts must understand and model pore geometries and fluid behaviors at pores scales more rapidly and realistically. We introduce an industry-unique direct hydrodynamic pore flow simulator that operates on pore geometries from digital rock models obtained using microCT or 3D scanning electron microscope (SEM) images. The PVT and rheological models used in the simulator represent real reservoir fluids. Fluid-solid interactions are introduced using distributed micro-scale wetting properties. The simulator uses density functional approach applied for hydrodynamics of complex systems. This talk covers selected applications of the simulator. We performed microCT scanning of six different carbonate rock samples from homogeneous limestones to vuggy carbonates. From these, we constructed digital rock models representing pore geometries for the simulator. We simulated nonreactive tracer flow in all six digital models using a digital fluid description that included a passive tracer solution. During the simulation, we evaluated the composition of the effluent. Results of tracer flow simulations corresponded well with experimental data of nonreactive tracer floods for the same carbonate rock types. This simulation data of the non-reactive tracer flow can be used to calculate the volume of the rock accessible by the fluid, which can be further used to predict response of a porous medium to a reactive fluid. The described digital core analysis workflow provides a basis for a wide variety of activities, including input to design acidizing jobs and evaluating treatment efficiency and EOR economics. Digital rock multiphase flow simulations of a scanned carbonate rock evaluated the effect of wettability on flow properties. Various wetting properties were tested: slightly oil wet, slightly water wet, and water wet. Steady-state relative permeability simulations yielded curves for all three ranges of wetting properties. The wetting variation affected phase mobility and residual phase saturations for primary oil flood and floods with varying ratios of oil and water.
Paleoweathering features in the Sergi Formation (Jurassic-Cretaceous), northeastern Brazil, and implications for hydrocarbon exploration

NASA Astrophysics Data System (ADS)

Pierini, Cristina; Mizusaki, Ana M.; Pimentel, Nuno; Faccini, Ubiratan F.; Scherer, Claiton M. S.

2010-03-01

Paleoweathering in the Sergi Formation has been classified and analyzed to ascertain its origin and relationship with stratigraphic evolution. The Sergi Formation belongs to the pre-rift sequence of the Recôncavo Basin (northeastern Brazil) and comprises a complex association of eolian and fluvial sandstones and lacustrine mudstones. This formation can be subdivided into three depositional sequences bounded by regional unconformities. Four paleoweathering types, each one related to a distinct origin, have been described in the Sergi Formation: (1) textural mottling, which is distinguished by alternating rock colors as a result of the iron oxide mobilization within mineral phases that evolved under alternating oxidation (yellowish, brownish and reddish shades) and reduction (grayish or greenish hues) conditions; (2) non-textural mottling, which displays a discoloration pattern that is independent of the original rock texture; (3) carbonate concentrations, usually related to carbonate nodule formation, which display a massive internal structure that reveals their origin through continuous growth or crystallization; and (4) banded carbonates (silicified), associated with the beginning of regular surface formation due to the chemical precipitation of carbonates within lacustrine environments. Both mottling color motifs and carbonate accumulation usually represent groundwater oscillation rather than pedogenesis. Only carbonate intraclasts and banded carbonate (silicified) have their origin ascribed to pedogenesis sensu stricto, although the carbonate intraclasts do not represent soil deposits in situ, but calcretes eroded from areas close to channels, and the banded carbonates (silicified) have strong diagenetic modifications. Therefore, it is reasonable to assume that fluvial and meteoric water have controlled paleoweathering evolution as well as deposition, yet both aspects are ruled by the same mechanisms (relief, sedimentation rate and, above all, climate).
The stratigraphy of the Steep Rock Group, N.W. Ontario, with evidence of a major unconformity

NASA Technical Reports Server (NTRS)

Wilks, M. E.; Nisbet, E. G.

1986-01-01

The Steep Rock Group is exposed 6 km north of Atikokan, 200 km west of Thunder Bay. It is situated on the southern margin of the Wabigoon Belt of the Archaean Superior Province, N. W. Ontario. Reinvestigation of the geology of the Group has shown that the Group lies unconformably on the Tonalite Complex to the east. This unconformity has been previously suspected, from regional and ine mapping but no conclusive outcrop evidence for its existence has as yet been published. The strike of the group, comprised of Basal Conglomerate, Carbonate Member, Ore Zone and Ashrock is generally north-northwest dipping steeply to the southwest. Of the 7 contacts between the Steep Rock Group and the Tonalite Complex, 3 expose the unconformity (The Headland, S. Roberts Pit, Trueman Point), and 4 are faulted. These three outcrops demonstrate unequivocally that the Steep Rock group was laid down unconformably on the underlying Tonalite Complex, which is circa 3 Ga old.
Evaluating of the spatial heterogeneity of soil loss tolerance and its effects on erosion risk in the carbonate areas of southern China

NASA Astrophysics Data System (ADS)

Li, Yue; Bai, Xiao Yong; Jie Wang, Shi; Qin, Luo Yi; Chao Tian, Yi; Jie Luo, Guang

2017-05-01

Soil loss tolerance (T value) is one of the criteria in determining the necessity of erosion control measures and ecological restoration strategy. However, the validity of this criterion in subtropical karst regions is strongly disputed. In this study, T value is calculated based on soil formation rate by using a digital distribution map of carbonate rock assemblage types. Results indicated a spatial heterogeneity and diversity in soil loss tolerance. Instead of only one criterion, a minimum of three criteria should be considered when investigating the carbonate areas of southern China because the one region, one T value concept may not be applicable to this region. T value is proportionate to the amount of argillaceous material, which determines the surface soil thickness of the formations in homogenous carbonate rock areas. Homogenous carbonate rock, carbonate rock intercalated with clastic rock areas and carbonate/clastic rock alternation areas have T values of 20, 50 and 100 t/(km2 a), and they are extremely, severely and moderately sensitive to soil erosion. Karst rocky desertification (KRD) is defined as extreme soil erosion and reflects the risks of erosion. Thus, the relationship between T value and erosion risk is determined using KRD as a parameter. The existence of KRD land is unrelated to the T value, although this parameter indicates erosion sensitivity. Erosion risk is strongly dependent on the relationship between real soil loss (RL) and T value rather than on either erosion intensity or the T value itself. If RL > > T, then the erosion risk is high despite of a low RL. Conversely, if T > > RL, then the soil is safe although RL is high. Overall, these findings may clarify the heterogeneity of T value and its effect on erosion risk in a karst environment.
Biodiversity on the Rocks: Macrofauna Inhabiting Authigenic Carbonate at Costa Rica Methane Seeps

PubMed Central

Levin, Lisa A.; Mendoza, Guillermo F.; Grupe, Benjamin M.; Gonzalez, Jennifer P.; Jellison, Brittany; Rouse, Greg; Thurber, Andrew R.; Waren, Anders

2015-01-01

Carbonate communities: The activity of anaerobic methane oxidizing microbes facilitates precipitation of vast quantities of authigenic carbonate at methane seeps. Here we demonstrate the significant role of carbonate rocks in promoting diversity by providing unique habitat and food resources for macrofaunal assemblages at seeps on the Costa Rica margin (400–1850 m). The attendant fauna is surprisingly similar to that in rocky intertidal shores, with numerous grazing gastropods (limpets and snails) as dominant taxa. However, the community feeds upon seep-associated microbes. Macrofaunal density, composition, and diversity on carbonates vary as a function of seepage activity, biogenic habitat and location. The macrofaunal community of carbonates at non-seeping (inactive) sites is strongly related to the hydrography (depth, temperature, O2) of overlying water, whereas the fauna at sites of active seepage is not. Densities are highest on active rocks from tubeworm bushes and mussel beds, particularly at the Mound 12 location (1000 m). Species diversity is higher on rocks exposed to active seepage, with multiple species of gastropods and polychaetes dominant, while crustaceans, cnidarians, and ophiuroids were better represented on rocks at inactive sites. Macro-infauna (larger than 0.3 mm) from tube cores taken in nearby seep sediments at comparable depths exhibited densities similar to those on carbonate rocks, but had lower diversity and different taxonomic composition. Seep sediments had higher densities of ampharetid, dorvilleid, hesionid, cirratulid and lacydoniid polychaetes, whereas carbonates had more gastropods, as well as syllid, chrysopetalid and polynoid polychaetes. Stable isotope signatures and metrics: The stable isotope signatures of carbonates were heterogeneous, as were the food sources and nutrition used by the animals. Carbonate δ13Cinorg values (mean = -26.98‰) ranged from -53.3‰ to +10.0‰, and were significantly heavier than carbonate δ13Corg (mean = -33.83‰), which ranged from -74.4‰ to -20.6‰. Invertebrates on carbonates had average δ13C (per rock) = -31.0‰ (range -18.5‰ to -46.5‰) and δ15N = 5.7‰ (range -4.5‰ to +13.4‰). Average δ13C values did not differ between active and inactive sites; carbonate fauna from both settings depend on chemosynthesis-based nutrition. Community metrics reflecting trophic diversity (SEAc, total Hull Area, ranges of δ13C and δ15N) and species packing (mean distance to centroid, nearest neighbor distance) also did not vary as a function of seepage activity or site. However, distinct isotopic signatures were observed among related, co-occurring species of gastropods and polychaetes, reflecting intense microbial resource partitioning. Overall, the substrate and nutritional heterogeneity introduced by authigenic seep carbonates act to promote diverse, uniquely adapted assemblages, even after seepage ceases. The macrofauna in these ecosystems remain largely overlooked in most surveys, but are major contributors to biodiversity of chemosynthetic ecosystems and the deep sea in general. PMID:26158723
The influence of carbonates in parent rocks on the biological properties of mountain soils of the Northwest Caucasus region

NASA Astrophysics Data System (ADS)

Kazeev, K. Sh.; Kutrovskii, M. A.; Dadenko, E. V.; Vezdeneeva, L. S.; Kolesnikov, S. I.; Val'kov, V. F.

2012-03-01

The biological activity of different subtypes of soddy-calcareous soils (rendzinas) of the Northwest Caucasus region was studied. In the Novorossiisk-Abrau-Dyurso region (dry subtropics), typical soddy-calcareous soils with the high content of carbonates predominate; in the more humid conditions of the Lagonaki Plateau (Republic of Adygeya), leached soddy-calcareous soils carbonate-free down to the parent rock are spread. The number of microarthropods, the populations of fungi and bacteria, and the enzyme activity (catalase, dehydrogenase, and invertase) testify that the biological activity of these soils significantly differs. In the typical soddy-calcareous soils of the dry subtropics, the content of carbonates does not affect the characteristics mentioned; in the more humid conditions of the West Caucasus region, the presence of carbonates in the parent rocks intensifies the biological activity of the soddy-calcareous soils.
Water resources of Oley Township, Berks County, Pennsylvania

USGS Publications Warehouse

Paulachok, G.N.; Wood, C.R.

1988-01-01

Oley Township covers an area of 24 square miles, about half of which is underlain by highly permeable carbonate rocks. Nondomestic wells in these rocks typically have yields of 200 gallons per minute, and some wells yield more than 1,000 gallons per minute. Ground-water yield for Oley Township is about 0.5 million gallons per day per square mile. Thus, about 12 million gallons per day could be pumped from wells on a sustained basis. However, pumping this amount would adversely affect streamflow. A series of discharge measurements on Manatawny Creek in January 1983 showed that the creek was gaining approximately 12 cubic feet per second where it crosses the more- permeable carbonate rocks. Thus, the streams are directly connected to these aquifers. The northern and western parts of the township are mostly underlain by shale, quartzite, granite, gneiss, and carbonate rocks of low permeability, and some wells do not yield enough water for domestic supplies. A water-table map shows that two active quarries in low-permeability rocks have had little effect on the hydrologic system. Specific yields are about 4.5 percent for the carbonate rocks; 5 percent for quartzite, granite, and gneiss; 1 percent for the noncarbonate sedimentary rocks; and 1.5 percent for the Jacksonburg Limestone, which consists of argillaceous limestone. In 1982--a year of average precipitation--the ground-water contribution to total streamflow ranged from 56 to 88 percent. Basins with the highest percentage of carbonate rock contribute the largest amount of ground water to streamflow. Evapotranspiration averaged about 26 inches in 1982. Water loss was 32 inches in the Limekiln Creek basin; this suggests that about 6 inches of precipitation bypassed the Limekiln Creek gaging station as ground-water underflow. The most serious water-quality problems are excessive nitrate concentrations and bacterial contamination. Water from 3 of 19 wells in carbonate rocks had nitrate concentrations in excess of the U.S. Environmental Protection Agency maximum contaminant level of 10 milligrams per liter. Water from 5 of the 19 wells had fecal streptococci counts of more than 20 colonies per 100 milliliters. Although most agencies concerned with the protection of public health have not set limits for fecal streptococci, they are pathogenic, and their presence in drinking water is undesirable.
Influence of substrate rocks on Fe Mn crust composition

NASA Astrophysics Data System (ADS)

Hein, James R.; Morgan, Charles L.

1999-05-01

Principal Component and other statistical analyses of chemical and mineralogical data of Fe-Mn oxyhydroxide crusts and their underlying rock substrates in the central Pacific indicate that substrate rocks do not influence crust composition. Two ridges near Johnston Atoll were dredged repetitively and up to seven substrate rock types were recovered from small areas of similar water depths. Crusts were analyzed mineralogically and chemically for 24 elements, and substrates were analyzed mineralogically and chemically for the 10 major oxides. Compositions of crusts on phosphatized substrates are distinctly different from crusts on substrates containing no phosphorite. However, that relationship only indicates that the episodes of phosphatization that mineralized the substrate rocks also mineralized the crusts that grew on them. A two-fold increase in copper contents in crusts that grew on phosphatized clastic substrate rocks, relative to crusts on other substrate rock types, is also associated with phosphatization and must have resulted from chemical reorganization during diagenesis. Phosphatized crusts show increases in Sr, Zn, Ca, Ba, Cu, Ce, V, and Mo contents and decreases in Fe, Si, and As contents relative to non-phosphatized crusts. Our statistical results support previous studies which show that crust compositions reflect predominantly direct precipitation from seawater (hydrogenetic), and to lesser extents reflect detrital input and diagenetic replacement of parts of the older crust generation by carbonate fluorapatite.
Influence of substrate rocks on Fe-Mn crust composition

USGS Publications Warehouse

Hein, J.R.; Morgan, C.L.

1999-01-01

Principal Component and other statistical analyses of chemical and mineralogical data of Fe-Mn oxyhydroxide crusts and their underlying rock substrates in the central Pacific indicate that substrate rocks do not influence crust composition. Two ridges near Johnston Atoll were dredged repetitively and up to seven substrate rock types were recovered from small areas of similar water depths. Crusts were analyzed mineralogically and chemically for 24 elements, and substrates were analyzed mineralogically and chemically for the 10 major oxides. Compositions of crusts on phosphatized substrates are distinctly different from crusts on substrates containing no phosphorite. However, that relationship only indicates that the episodes of phosphatization that mineralized the substrate rocks also mineralized the crusts that grew on them. A two-fold increase in copper contents in crusts that grew on phosphatized clastic substrate rocks, relative to crusts on other substrate rock types, is also associated with phosphatization and must have resulted from chemical reorganization during diagenesis. Phosphatized crusts show increases in Sr, Zn, Ca, Ba, Cu, Ce, V, and Mo contents and decreases in Fe, Si, and As contents relative to non-phosphatized crusts. Our statistical results support previous studies which show that crust compositions reflect predominantly direct precipitation from seawater (hydrogenetic), and to lesser extents reflect detrital input and diagenetic replacement of parts of the older crust generation by carbonate fluorapatite.
Strontium isotopes as tracers of water-rocks interactions, mixing processes and residence time indicator of groundwater within the granite-carbonate coastal aquifer of Bonifacio (Corsica, France).

PubMed

Santoni, S; Huneau, F; Garel, E; Aquilina, L; Vergnaud-Ayraud, V; Labasque, T; Celle-Jeanton, H

2016-12-15

This study aims at identifying the water-rock interactions and mixing rates within a complex granite-carbonate coastal aquifer under high touristic pressure. Investigations have been carried out within the coastal aquifer of Bonifacio (southern Corsica, France) mainly composed of continental granitic weathering products and marine calcarenite sediments filling a granitic depression. A multi-tracer approach combining physico-chemical parameters, major ions, selected trace elements, stable isotopes of the water molecule and 87 Sr/ 86 Sr ratios measurements is undertaken for 20 groundwater samples during the low water period in November 2014. 5 rock samples of the sedimentary deposits and surrounding granites are also analysed. First, the water-rock interactions processes governing the groundwater mineralization are described in order to fix the hydrogeochemical background. Secondly, the flow conditions are refined through the quantification of inter aquifer levels mixing, and thirdly, the kinetics of water-rock interaction based on groundwater residence time from a previous study using CFCs and SF 6 are quantified for the two main flow lines. A regional contrast in the groundwater recharge altitude allowed the oxygene-18 to be useful combined with the 87 Sr/ 86 Sr ratios to differentiate the groundwater origins and to compute the mixing rates, revealing the real extension of the watershed and the availability of the resource. The results also highlight a very good correlation between the groundwater residence time and the spatial evolution of 87 Sr/ 86 Sr ratios, allowing water-rock interaction kinetics to be defined empirically for the two main flow lines through the calcarenites. These results demonstrate the efficiency of strontium isotopes as tracers of water-rock interaction kinetics and by extension their relevance as a proxy of groundwater residence time, fundamental parameter documenting the long term sustainability of the hydrosystem. Copyright Â© 2016 Elsevier B.V. All rights reserved.
Chronostratigraphy and hydrocarbon habitat associated with the Jurassic carbonates of Abu Dhabi, United Arab Emirates

DOE Office of Scientific and Technical Information (OSTI.GOV)

Alsharahan, A.S.; Whittle, G.L.

1995-08-01

Deposition of Jurassic epeiric shelf carbonates and evaporates were controlled by epeirogenic movement and sea level fluctuations which formed an excellent combination of source rocks, reservoirs and seats in Abu Dhabi. At the end of the Triassic, a relative drop in sea level, caused by eustatic sea level lowering in conjunction with minor tectonic uplift, resulted in non-deposition or erosion. In the Toarcian, deposition of carbonates and terrigenous, clastics produced the Marrat Formation. In the mid-Aalenian, a drop in sea level eroded much of the Marrat and some of the Triassic in offshore U.A.E. The deposition of the Hamlah Formationmore » followed, under neritic, well-oxygenated conditions. The Middle Jurassic was characterized by widespread, normal marine shelf carbonates which formed the cyclic Izhara and Araej formations (reservoirs). In the Upper Jurassic, the carbonate shelf became differentiated into a broad shelf with a kerogen-rich intrashelf basin, formed in response to a eustatic rise coupled with epeirogenic downwarping and marine flooding. The intrashelf basin fill of muddy carbonate sediments constitutes the Diyab Formation and its onshore equivalent, the Dukhan Formation (source rocks). In the late Upper Jurassic, the climate became more arid and cyclic deposition of carbonates and evaporates prevailed, forming alternating peritidal anhydrite, dolomite and limestone in the Arab Formation (reservoir). Arid conditions continued into the Tithonian, fostering the extensive anhydrite of the Hith Formation (seal) in a sabkha/lagoonal setting on the shallow peritidal platform, the final regressive supratidal stage of this major depositional cycle.« less
Capillary Trapping of CO2 in Oil Reservoirs: Observations in a Mixed-Wet Carbonate Rock.

PubMed

Al-Menhali, Ali S; Krevor, Samuel

2016-03-01

Early deployment of carbon dioxide storage is likely to focus on injection into mature oil reservoirs, most of which occur in carbonate rock units. Observations and modeling have shown how capillary trapping leads to the immobilization of CO2 in saline aquifers, enhancing the security and capacity of storage. There are, however, no observations of trapping in rocks with a mixed-wet-state characteristic of hydrocarbon-bearing carbonate reservoirs. Here, we found that residual trapping of supercritical CO2 in a limestone altered to a mixed-wet state with oil was significantly less than trapping in the unaltered rock. In unaltered samples, the trapping of CO2 and N2 were indistinguishable, with a maximum residual saturation of 24%. After the alteration of the wetting state, the trapping of N2 was reduced, with a maximum residual saturation of 19%. The trapping of CO2 was reduced even further, with a maximum residual saturation of 15%. Best-fit Land-model constants shifted from C = 1.73 in the water-wet rock to C = 2.82 for N2 and C = 4.11 for the CO2 in the mixed-wet rock. The results indicate that plume migration will be less constrained by capillary trapping for CO2 storage projects using oil fields compared with those for saline aquifers.
Carbon sequestration via reaction with basaltic rocks: geochemical modeling and experimental results

USGS Publications Warehouse

Rosenbauer, Robert J.; Thomas, Burt; Bischoff, James L.; Palandri, James

2012-01-01

Basaltic rocks are potential repositories for sequestering carbon dioxide (CO2) because of their capacity for trapping CO2 in carbonate minerals. We carried out a series of thermodynamic equilibrium models and high pressure experiments, reacting basalt with CO2-charged fluids over a range of conditions from 50 to 200 °C at 300 bar. Results indicate basalt has a high reactivity to CO2 acidified brine. Carbon dioxide is taken up from solution at all temperatures from 50 to 200 °C, 300 bar, but the maximum extent and rate of reaction occurs at 100 °C, 300 bar. Reaction path simulations utilizing the geochemical modeling program CHILLER predicted an equilibrium carbonate alteration assemblage of calcite, magnesite, and siderite, but the only secondary carbonate identified in the experiments was a ferroan magnesite. The amount of uptake at 100 °C, 300 bar ranged from 8% by weight for a typical tholeite to 26% for a picrite. The actual amount of CO2 uptake and extent of rock alteration coincides directly with the magnesium content of the rock suggesting that overall reaction extent is controlled by bulk basalt Mg content. In terms of sequestering CO2, an average basaltic MgO content of 8% is equivalent to 2.6 × 108 metric ton CO2/km3 basalt.
Graphite-(Mo,W)S2 intergrowth as a palaeoenvironmental proxy in metasedimentary rocks

NASA Astrophysics Data System (ADS)

Cabral, Alexandre Raphael; Zeh, Armin; da Silva Viana, Nívea Cristina; Schirmer, Thomas; Lehmann, Bernd

2017-12-01

Molybdenum enrichment in pristine organic-C-rich sedimentary rocks forms the basis for inferring the presence of dissolved oxygen in seawater. Organic matter removes dissolved hexavalent Mo from seawater where anoxic and euxinic conditions are attained. However, it is unknown whether this Mo-based proxy is retained under metamorphic conditions where organic C is no longer preserved. Here, we describe aggregates of graphite and molybdenite (MoS2) containing up to 21 mass per cent of W as tungstenite (WS2) in solid solution. These aggregates are disseminated in a sulfide-rich Mn-silicate-carbonate rock (queluzite), metamorphosed under amphibolite-facies conditions within the Archaean Barbacena greenstone belt in Minas Gerais, Brazil. Our finding indicates that: (i) W is, like Mo, a palaeoenvironmental proxy; (ii) the W proxy is sensitive to high fS2/fO2 environments; (iii) both Mo and W proxies survive amphibolite-facies overprint as (Mo,W)S2 intergrown with graphite. Archaean greenstones are potential candidates for storing palaeoenvironmental information as (Mo,W)S2-graphite intergrowths.
Endolithic Boring Enhance the Deep-sea Carbonate Lithification on the Southwest Indian Ridge

NASA Astrophysics Data System (ADS)

Peng, X.; Xu, H.

2017-12-01

Deep-sea carbonates represent an important type of sedimentary rock due to their effect on the composition of upper oceanic crust and their contribution to deep-sea geochemical cycles. However, the lithification of deep-sea carbonates at the seafloor has remained a mystery for many years. A large lithified carbonate area, characterized by thriving benthic faunas and tremendous amount of endolithic borings, was discovered in 2008, blanketed on the seafloor of ultraslow spreading Southwest Indian Ridge (SWIR). Macrofaunal inhabitants including echinoids, polychaetes, gastropods as well as crustaceans, are abundant in the sample. The most readily apparent feature of the sample is the localized enhancement of density around the borings. The boring features of these carbonate rocks and factors that may enhance deep-sea carbonate lithification are reported. The δ13CPDB values of 46 bulk samples are -0.37 to 1.86‰, while these samples have a relatively narrow δ18OPDB range of 1.35 to 3.79‰. The bulk δ13CPDB values of chalk and gray excrements are positively correlated with bulk δ18OPDB values (r = 0.91) (Fig. 8), which reflects that endolithic boring is possibly a critical factor influence the lithification. We suggest that active boring may trigger the dissolution of the original calcite and thus accelerate deep-sea carbonate lithification on mid-ocean ridges. Our study reports an unfamiliar phenomenon of non-burial carbonate lithification and interested by the observation that it is often associated with boring feature. These carbonate rocks may provide a novel mechanism for deep-sea carbonate lithification at the deep-sea seafloor and also illuminate the geological and biological importance of deep-sea carbonate rocks on mid-ocean ridges.
Multiphase flow of carbon dioxide and brine in dual porosity carbonates

NASA Astrophysics Data System (ADS)

Pentland, Christopher; Oedai, Sjaam; Ott, Holger

2014-05-01

The storage of carbon dioxide in subsurface formations presents a challenge in terms of multiphase flow characterisation. Project planning requires an understanding of multiphase flow characteristics such as the relationship between relative permeability and saturation. At present there are only a limited number of relative permeability relations for carbon dioxide-brine fluid systems, most of which are measured on sandstone rocks. In this study coreflood experiments are performed to investigate the relative permeability of carbon dioxide and brine in two dual porosity carbonate systems. Carbon dioxide is injected into the brine saturated rocks in a primary drainage process. The rock fluid system is pre-equilibrated to avoid chemical reactions and physical mass transfer between phases. The pressure drop across the samples, the amount of brine displaced and the saturation distribution within the rocks are measured. The experiments are repeated on the same rocks for the decane-brine fluid system. The experimental data is interpreted by simulating the experiments with a continuum scale Darcy solver. Selected functional representations of relative permeability are investigated, the parameters of which are chosen such that a least squares objective function is minimised (i.e. the difference between experimental observations and simulated response). The match between simulation and measurement is dependent upon the form of the functional representations. The best agreement is achieved with the Corey [Brooks and Corey, 1964] or modified Corey [Masalmeh et al., 2007] functions which best represent the relative permeability of brine at low brine saturations. The relative permeability of carbon dioxide is shown to be lower than the relative permeability of decane over the saturation ranges investigated. The relative permeability of the brine phase is comparable for the two fluid systems. These observations are consistent with the rocks being water-wet. During the experiment only a portion of the full saturation range is investigated, corresponding to carbon dioxide entering the macro pores of the dual porosity systems. Within this pore space the relative permeability behaviour is comparable to that measured in Berea sandstone. Brooks, R. H., and A. T. Corey (1964), Hydraulic properties of porous media, Hydrology Papers 3, Civil Engineering Dept., Colorado State Univ., Fort Collins, CO. Masalmeh, S., I. Abu-Shiekah, and X. Jing (2007), Improved Characterization and Modeling of Capillary Transition Zones in Carbonate Reservoirs, SPE Reserv. Eval. Eng., 10(2), doi:10.2118/109094-PA.
Ground-water quality in the carbonate-rock aquifer of the Great Basin, Nevada and Utah, 2003

USGS Publications Warehouse

Schaefer, Donald H.; Thiros, Susan A.; Rosen, Michael R.

2005-01-01

The carbonate-rock aquifer of the Great Basin is named for the thick sequence of Paleozoic limestone and dolomite with lesser amounts of shale, sandstone, and quartzite. It lies primarily in the eastern half of the Great Basin and includes areas of eastern Nevada and western Utah as well as the Death Valley area of California and small parts of Arizona and Idaho. The carbonate-rock aquifer is contained within the Basin and Range Principal Aquifer, one of 16 principal aquifers selected for study by the U.S. Geological Survey’s National Water- Quality Assessment Program.Water samples from 30 ground-water sites (20 in Nevada and 10 in Utah) were collected in the summer of 2003 and analyzed for major anions and cations, nutrients, trace elements, dissolved organic carbon, volatile organic compounds (VOCs), pesticides, radon, and microbiology. Water samples from selected sites also were analyzed for the isotopes oxygen-18, deuterium, and tritium to determine recharge sources and the occurrence of water recharged since the early 1950s.Primary drinking-water standards were exceeded for several inorganic constituents in 30 water samples from the carbonate-rock aquifer. The maximum contaminant level was exceeded for concentrations of dissolved antimony (6 μg/L) in one sample, arsenic (10 μg/L) in eleven samples, and thallium (2 μg/L) in one sample. Secondary drinking-water regulations were exceeded for several inorganic constituents in water samples: chloride (250 mg/L) in five samples, fluoride (2 mg/L) in two samples, iron (0.3 mg/L) in four samples, manganese (0.05 mg/L) in one sample, sulfate (250 mg/L) in three samples, and total dissolved solids (500 mg/L) in seven samples.Six different pesticides or metabolites were detected at very low concentrations in the 30 water samples. The lack of VOC detections in water sampled from most of the sites is evidence thatVOCs are not common in the carbonate-rock aquifer. Arsenic values for water range from 0.7 to 45.7 μg/L, with a median value of 9.6 μg/L. Factors affecting arsenic concentration in the carbonate-rock aquifer in addition to geothermal heating are its natural occurrence in the aquifer material and time of travel along the flow path.Most of the chemical analyses, especially for VOCs and nutrients, indicate little, if any, effect of overlying land-use patterns on ground-water quality. The water quality in recharge areas for the aquifer where human activities are more intense may be affected by urban and/or agricultural land uses as evidenced by pesticide detections. The proximity of the carbonate-rock aquifer at these sites to the land surface and the potential for local recharge to occur through the fractured rock likely results in the occurrence of these and other land-surface related contaminants in the ground water. Water from sites sampled near outcrops of carbonate-rock aquifer likely has a much shorter residence time resulting in a potential for detection of anthropogenic or land-surface related compounds. Sites located in discharge areas of the flow systems or wells that are completed at a great depth below the land surface generally show no effects of land-use activities on water quality. Flow times within the carbonate-rock aquifer, away from recharge areas, are on the order of thousands of years, so any contaminants introduced at the land surface that will not degrade along the flow path have not reached the sampled sites in these areas.
Origin of karst conduits in calcareous sandstone and carbonate-silicate rocks: Complex role of insoluble material

NASA Astrophysics Data System (ADS)

Bruthans, Jiri; Balak, Frantisek; Schweigstillova, Jana; Vojtisek, Jan

2017-04-01

Carbonate karst is best developed in high-grade limestones and majority of the studies is focused on these rocks. Features developed by dissolution of calcite cement in quartz sandstones and dissolution of various carbonate-silicate rocks are studied far less frequently. Unlike in common karst, the insoluble residuum has to be washed out after dissolution to create high-permeability conduits in these rocks. Aquifers in a Bohemian Cretaceous Basin (BCB), the most important hydrogeological basin in the Czech Republic, consist mainly of quartz and calcareous sandstones to siltstones. These rocks are intercalated by thin layers of calcite-cemented sandstone and low-grade limestone, the latter sometimes partly impregnated by a secondary silica. Results of tracer tests show a high flow velocity in some of the aquifers. Springs with flow rate up to 500 l/s and wells with yield up to 200 l/s occur in these rocks. Dissolution features in BCB were however not yet studied in detail. For identification and characterization of rocks prone to karstification, 350 cores were sampled mostly from boreholes but also from rock outcrops in several areas of BCB. Cores were taken from intervals where: (i) high carbonate content was expected, (ii) conduits and enlarged porosity was observed in rock outcrops or wells, (iii) inflows to boreholes were determined by well logging. Calcium carbonate content was determined by calcimetry in all cores. All cores were leached in hydrochloric acid to observe the degree of disintegration after removal of calcite, which was far dominating portion of total carbonate. Polished sections were prepared from selected cores and Ca, Si, Na, K, Al content was automatically mapped by microprobe to visualize the calcium, silica, feldspar and clay mineral distribution in cores. Conduits were photo documented in the field. Two types of sediments with distinct disintegration characteristics were observed: (i) In sandstone composed of quartz grains cemented by calcite the complete disintegration occurs when calcite content exceeds 30-50%. Such calcite-rich layers are mostly few tens of cms thick and are enclosed in quartz sandstone. Groundwater flow dissolves calcite cement and turns the rock into cohesion-less sand. Sand is consequently washed out by headward erosion in drainage areas forming high capacity conduits within the sandstone. (ii) In carbonates containing secondary silica which form reinforcing structure, even 70-80% calcite content may not be sufficient for rock disintegration during leaching. Disintegration occurs only on tectonically heavily fractured zones, where secondary silica structure is fragmented. It was found that inflows into wells are often associated with zones prone to karstification. Results clearly show that form of insoluble material is critical for karstification potential. Insoluble grain size defines minimum flow velocity needed to excavate the conduits in dissolved residuum. Impregnation by secondary silica needs to be tectonically fragmented prior conduits can occur. Research was funded by the Czech Science Foundation (GA CR No. 16-19459S) and Review of groundwater resources (Ident. No. 155996).
Mineral dissolution and precipitation in carbonate dominated terranes assessed using Mg isotopes

NASA Astrophysics Data System (ADS)

Tipper, E.; Calmels, D.; Gaillardet, J.; Galy, A.

2013-12-01

Carbonate weathering by carbonic acid consumes atmospheric CO2 during mineral dissolution, fixing it as aqueous bicarbonate over millennial time-scales. Ocean acidification has increased the solubility of CO2 in seawater by changing the balance of pH to alkalinity (the oceanic reservoir of carbon). This has lengthened the time-scale for CO2 sequestration by carbonate weathering to tens of thousands of years. At a global scale, the net consumption of CO2 is at least equal to that from silicate weathering, but there is far less work on carbonate weathering compared to silicate weathering because it has generally been assumed to be CO2 neutral on geological time-scales. Carbonate rocks are more readily dissolved than silicate rocks, meaning that their dissolution will likely respond much more rapidly to global environmental change when compared with the dissolution of silicate minerals. Although far less concentrated than Ca in many carbonates, Mg substitutes for Ca and is more concentrated than any other metal ion. Tracing the behavior of Mg in river waters, using Mg stable isotopes (26Mg/24Mg ratio expressed as delta26Mg in per mil units) is therefore a novel way to understand the complex series of dissolution/precipitation reactions that govern solute concentrations of Ca and Mg, and hence CO2 transfer by carbonate weathering. We present new Mg isotope data on a series of river and spring waters from the Jura mountains in North-East France. The stratigraphic column is relatively uniform throughout the Jura mountains and is dominated by limestones. As the limestone of the Jura Mountains were deposited in high-energy shallow water environments (shore line, lagoon and coral reefs), they are usually clay and organic poor. The delta26Mg of the local rocks is very constant at circa -4permil. The delta26Mg of the river waters is also fairly constant, but offset from the rock at -2.5permil. This is an intriguing observation because the dissolution of limestones is expected to be congruent, meaning that the Mg released to solutes during mineral dissolution should have the same composition as the host rock. Some of this difference is likely accounted for by atmospheric deposition or cyclic inputs, but this cannot account for all of the 1.5permil shift between rock and water. It is plausible that some of the difference is explained by trace levels of Mg-silicate dissolution (with a delta26Mg of circa 0permil), but equally carbonate precipitation and attendant Mg isotope fractionation could theoretically account for the difference between rock and water. The various plausible explications will be discussed, as well as the implications of the data for better understanding carbonate weathering.
Fluid-absent metamorphism in the Adirondacks

NASA Technical Reports Server (NTRS)

Valley, J. W.

1986-01-01

Results on late Proterozoic metamorphism of granulite in the Adirondacks are presented. There more than 20,000 sq km of rock are at granulite facies. Low water fugacites are implied by orthopyroxene bearing assemblages and by stability of k'spar-plag-quartz assemblages. After mentioning the popular concept of infiltration of carbon dioxide into Precambrian rocks and attendent generation of granulite facies assemblages, several features of Adirondack rocks pertinent to carbon dioxide and water during their metamorphism are summarized: wollastonite occurs in the western lowlands; contact metamorphism by anorthosite preceeding granulite metamorphism is indicated by oxygen isotopes. Oxygen fugacity lies below that of the QFM buffer; total P sub water + P sub carbon dioxide determined from monticellite bearing assemblages are much less than P sub total (7 to 7.6 kb). These and other features indicate close spatial association of high- and low-P sub carbon dioxide assemblages and that a vapor phase was not present during metamorphism. Thus Adirondack rocks were not infiltrated by carbon dioxide vapor. Their metamorphism, at 625 to 775 C, occurred either when the protoliths were relatively dry or after dessication occurred by removal of a partial melt phase.

What controls diffuse fractures in platform carbonates? Insights from Provence (France) and Apulia (Italy)

NASA Astrophysics Data System (ADS)

Lavenu, Arthur P. C.; Lamarche, Juliette

2018-03-01

Fractures are widespread in rocks and regional opening-mode arrays are commonly ascribed to major tectonic events. However, fractures occur in otherwise undeformed rocks. Some of these are early-developed features independent of tectonics and forming a background network at regional scale. To overcome this lack of understanding, two hydrocarbon reservoir analogues from platform carbonates have been targeted: the Provence (SE France), and the Apulian platform (SE Italy). In both areas, an early fracturing stage has been observed, made of high-angle-to-bedding opening-mode fractures, and bed-parallel stylolites. These features developed synchronously during the first burial stages and prior to major tectonic events. The fracture sets are not genetically related to the present-day layering. Contrarily, fractures developed in a brittle media where facies transitions were not sharp and did not act as mechanical discontinuities. Carbonate facies distribution and early diagenetic imprint constrained the mechanical stratigraphy when fractures occurred. In addition, we observed that fractures related to late tectonic inversion were partly inhibited. Indeed, rock mechanical properties change through time. Characterizing the temporal evolution of carbonate rocks has revealed that diagenesis and sedimentary facies are the prime actors for brittleness and mechanical layering in carbonates.
Orbital evidence for more widespread carbonate-bearing rocks on Mars

NASA Astrophysics Data System (ADS)

Wray, James J.; Murchie, Scott L.; Bishop, Janice L.; Ehlmann, Bethany L.; Milliken, Ralph E.; Wilhelm, Mary Beth; Seelos, Kimberly D.; Chojnacki, Matthew

2016-04-01

Carbonates are key minerals for understanding ancient Martian environments because they are indicators of potentially habitable, neutral-to-alkaline water and may be an important reservoir for paleoatmospheric CO2. Previous remote sensing studies have identified mostly Mg-rich carbonates, both in Martian dust and in a Late Noachian rock unit circumferential to the Isidis basin. Here we report evidence for older Fe- and/or Ca-rich carbonates exposed from the subsurface by impact craters and troughs. These carbonates are found in and around the Huygens basin northwest of Hellas, in western Noachis Terra between the Argyre basin and Valles Marineris, and in other isolated locations spread widely across the planet. In all cases they cooccur with or near phyllosilicates, and in Huygens basin specifically they occupy layered rocks exhumed from up to ~5 km depth. We discuss factors that might explain their observed regional distribution, arguments for why carbonates may be even more widespread in Noachian materials than presently appreciated and what could be gained by targeting these carbonates for further study with future orbital or landed missions to Mars.
Decrypting the Formation Conditions of the Basement Carbonate-Bearing Rocks at Nili Fossae

NASA Astrophysics Data System (ADS)

Brown, A. J.

2015-12-01

The Nili Fossae region is the site of a number of proposed Landing Sites for the Mars 2020 Rover. A distinguishing feature of many of these sites is the access to large exposures of carbonate (Ehlmann et al. 2008). Serpentinization has been proposed as a formation mechanism of these carbonates, including carbonated (Brown et al. 2010, Viviano, et al. 2013) and low temperature, near surface serpentinization. The potential for carbonated serpentization at Nili Fossae links the region to Earth analogs in terrestrial greenstone belts such as the Pilbara in Western Australia, where talc-carbonate bearing komatiite cumulate units of the Dresser Formation overlie the siliceous, stromatolite-bearing Strelley Pool Chert unit (Van Kranendonk and Pirajno, 2004). If a similar relationship exists on Mars, investigations of rocks stratigraphically beneath the carbonate-bearing units at Nili Fossae ("the basement rocks") may provide the best chance to examine well preserved organic material from the Noachian. This hypothesis is testable by Mars 2020. In preparation for the the Mars 2020 landing site, we are examining the thermodynamic relationships that favor formation of serpentine and talc-carbonate and different pressures and temperatures in the crust (Barnes 2007). This will allow us to constrain the low grade metamorphism required to replicate the proposed models of serpentinisation and help us understand the regional metamophic gradient that is critical to furthering our knowledge of the ancient rocks of Nili Fossae. Refs:Barnes, S. J. "Komatiites: Petrology, Volcanology, Metamorphism, and Geochemistry." S.E.G. 13 (2007): 13. Brown, A. J., et al.. "Hydrothermal Formation of Clay-Carbonate Alteration Assemblages in the Nili Fossae Region of Mars." EPSL 297 (2010): 174-82. Ehlmann, B. L. et al. "Orbital Identification of Carbonate-Bearing Rocks on Mars." Science 322, no. 5909 1828-32. Van Kranendonk, M.J., and F. Pirajno. "Geochemistry of Metabasalts and Hydrothermal Alteration Zones Associated with Ca. 3.45 Ga Chert+/- Barite Deposits" GEEA 4, no. 3 (2004): 253-78. Viviano, C. E., et al. "Implications for Early Hydrothermal Environments on Mars through the Spectral Evidence for Carbonation and Chloritization Reactions in the Nili Fossae Region." JGR 118, no. 9 (2013): 1858-72.
The Pietra Grande thrust (Brenta Dolomites, Italy): looking for co-seismic indicators along a main fault in carbonate sequences

NASA Astrophysics Data System (ADS)

Viganò, Alfio; Tumiati, Simone; Martin, Silvana; Rigo, Manuel

2013-04-01

At present, pseudotachylytes (i.e. solidified frictional melts) are the only unambiguous geological record of seismic faulting. Even if pseudotachylytes are frequently observed along faults within crystalline rocks they are discovered along carbonate faults in very few cases only, suggesting that other chemico-physical processes than melting could occur (e.g. thermal decomposition). In order to investigate possible co-seismic indicators we study the Pietra Grande thrust, a carbonate fault in the Brenta Dolomites (Trentino, NE Italy), to analyse field structure, microtextures and composition of rocks from the principal slip plane, the fault core and the damage zone. The Pietra Grande thrust is developed within limestones and dolomitic limestones of Late Triassic-Early Jurassic age (Calcari di Zu and Monte Zugna Formations). The thrust, interpreted as a north-vergent décollement deeply connected with the major Cima Tosa thrust, is a sub-horizontal fault plane gently dipping to the North that mainly separates the massive Monte Zugna Fm. limestones (upper side) from the stratified Calcari di Zu Fm. limestones with intercalated marls (lower side). On the western face of the Pietra Grande klippe the thrust is continuously well-exposed for about 1 km. The main fault plane shows reddish infillings, which form veins with thicknesses between few millimetres to several decimetres. These red veins lie parallel to the thrust plane or in same cases inject lateral fractures and minor high-angle faults departing from the main fault plane. Veins have carbonate composition and show textures characterized by fine-grained reddish matrix with embedded carbonate clasts of different size (from few millimetres to centimetres). In some portions carbonate boulders (dimension of some decimetres) are embedded in the red matrix, while clast content generally significantly decreases at the vein borders (chilled margins). Red veins are typically associated with cohesive cataclasites and/or breccias of the fault zone. Host and fault rocks are locally folded, with fold axes having a rough E-W direction compatible with simultaneous thrust activation, suggesting deformation under brittle-ductile conditions. A late brittle deformation is testified by near-vertical fractures and strike-slip faults (WNW-directed) intersecting the whole thrust system. Field structure, microtextures, chemical and mineralogical compositions of host rocks, cataclasites and breccias are analysed. In particular, red veins are carefully compared with the very similar Grigne carbonate pseudotachylytes (Viganò et al. 2011, Terra Nova, vol. 23, pp.187-194), in order to evaluate if they could represent a certain geological record of seismic faulting of the Pietra Grande thrust.
Stages of weathering mantle formation from carbonate rocks in the light of rare earth elements (REE) and Sr-Nd-Pb isotopes

NASA Astrophysics Data System (ADS)

Hissler, Christophe; Stille, Peter

2015-04-01

Weathering mantles are widespread and include lateritic, sandy and kaolinite-rich saprolites and residuals of partially dissolved rocks. These old regolith systems have a complex history of formation and may present a polycyclic evolution due to successive geological and pedogenetic processes that affected the profile. Until now, only few studies highlighted the unusual high content of associated trace elements in weathering mantles originating from carbonate rocks, which have been poorly studied, compared to those developing on magmatic bedrocks. For instance, these enrichments can be up to five times the content of the underlying carbonate rocks. However, these studies also showed that the carbonate bedrock content only partially explains the soil enrichment for all the considered major and trace elements. Up to now, neither soil, nor saprolite formation has to our knowledge been geochemically elucidated. Therefore, the aim of this study was to examine more closely the soil forming dynamics and the relationship of the chemical soil composition to potential sources. REE distribution patterns and Sr-Nd-Pb isotope ratios have been used because they are particularly well suited to identify trace element migration, to recognize origin and mixing processes and, in addition, to decipher possible anthropogenic and/or "natural" atmosphere-derived contributions to the soil. Moreover, leaching experiments have been applied to identify mobile phases in the soil system and to yield information on the stability of trace elements and especially on their behaviour in these Fe-enriched carbonate systems. All these geochemical informations indicate that the cambisol developing on such a typical weathering mantle ("terra fusca") has been formed through weathering of a condensed Bajocian limestone-marl facies. This facies shows compared to average world carbonates important trace element enrichments. Their trace element distribution patterns are similar to those of the soil suggesting their close genetic relationships. Sr-Nd-Pb isotope data allow to identify four principal components in the soil: a silicate-rich pool at close to the surface, a leachable REE enriched pool at the bottom of the soil profile, the limestone facies on which the weathering profile developed and an anthropogenic, atmosphere-derived component detected in the soil leachates of the uppermost soil horizon. The leachable phases are mainly secondary carbonate-bearing REE phases such as bastnaesite. The isotope data and trace element distribution patterns indicate that at least four geological and environmental events impacted the chemical and isotopical compositions of the soil system since the Cretaceous.
Smectite Formation from Basaltic Glass Under Acidic Conditions on Mars

NASA Technical Reports Server (NTRS)

Peretyazhko, T. S.; Sutter, B.; Morris, R. V.; Agresti, D. G.; Le, L.; Ming, D. W.

2015-01-01

Massive deposits of phyllosilicates of the smectite group, including Mg/Fe-smectite, have been identified in Mars's ancient Noachian terrain. The observed smectite is hypothesized to form through aqueous alteration of basaltic crust under neutral to alkaline pH conditions. These pH conditions and the presence of a CO2-rich atmosphere suggested for ancient Mars were favorable for the formation of large carbonate deposits. However, the detection of large-scale carbonate deposits is limited on Mars. We hypothesized that smectite deposits may have formed under acidic conditions that prevented carbonate precipitation. In this work we investigated formation of saponite at a pH of approximately 4 from Mars-analogue synthetic Adirondack basaltic glass of composition similar to Adirondack class rocks located at Gusev crater. Hydrothermal (200º Centigrade) 14 day experiments were performed with and without 10 millimoles Fe(II) or Mg under anoxic condition [hereafter denoted as anoxic_Fe, anoxic_Mg and anoxic (no addition of Fe(II) or Mg)] and under oxic condition [hereafter denoted as oxic (no addition of Fe(II) or Mg)]. Characterization and formation conditions of the synthesized saponite provided insight into the possible geochemical conditions required for saponite formation on Mars.
Origin of epigenetic calcite in coal from Antarctica and Ohio based on isotope compositions of oxygen, carbon and strontium

USGS Publications Warehouse

Faure, G.; Botoman, G.

1984-01-01

Isotopic compositions of oxygen, carbon and strontium of calcite cleats in coal seams of southern Victoria Land, Antarctica, and Tuscarawas County, Ohio, contain a record of the conditions a the time of their formation. The Antarctic calcites (?? 18O(SMOW) = +9.14 to +11.82%0) were deposited from waters enriched in 16O whose isotopic composition was consistent with that of meteoric precipitation at low temperature and high latitude. The carbon of the calcite cleats (?? 13C(PDB) = -15.6 to -16.9%0) was derived in part from the coal (?? 13C(PDB) = -23.5 to -26.7%0) as carbon dioxide and by oxidation of methane or other hydrocarbon gases. The strontium ( 87Sr 86Sr = 0.71318-0.72392) originated primarily from altered feldspar grains in the sandstones of the Beacon Supergroup. Calcite cleats in the Kittaning No. 6 coal seam of Ohio (?? 18O(SMOW) = +26.04 to +27.79%0) were deposited from waters that had previously exchanged oxygen, possibly with marine carbonate at depth. The carbon (?? 13C(PDB) = 0.9 to +2.4%0) is enriched in 13C even though that cleats were deposited in coal that is highly enriched in 12C and apparently originated from marine carbonates. Strontium in the cleats ( Sr 87 0.71182-0.71260) is not of marine origin but contains varying amounts of radiogenic 87Sr presumably derived from detrital Rb-bearing minerals in the adjacent sedimentary rocks. The results of this study suggest that calcite cleats in coal of southern Victoria Land, Antarctica, were deposited after the start of glaciation in Cenozoic time and that those in Ohio precipitated from formation waters derived from the underlying marine carbonate rocks, probably in the recent geologic past. ?? 1984.
Genome Sequence of Carbon Dioxide-Sequestering Serratia sp. Strain ISTD04 Isolated from Marble Mining Rocks.

PubMed

Kumar, Manish; Gazara, Rajesh Kumar; Verma, Sandhya; Kumar, Madan; Verma, Praveen Kumar; Thakur, Indu Shekhar

2016-10-20

The Serratia sp. strain ISTD04 has been identified as a carbon dioxide (CO 2 )-sequestering bacterium isolated from marble mining rocks in the Umra area, Rajasthan, India. This strain grows chemolithotrophically on media that contain sodium bicarbonate (NaHCO 3 ) as the sole carbon source. Here, we report the genome sequence of 5.07 Mb Serratia sp. ISTD04. Copyright © 2016 Kumar et al.
CO2 driven weathering vs plume driven weathering as inferred from the groundwater of a persistently degassing basaltic volcano: Mt. Etna

NASA Astrophysics Data System (ADS)

Liotta, Marcello; D'Alessandro, Walter

2016-04-01

At Mt. Etna the presence of a persistent volcanic plume provides large amounts of volcanogenic elements to the bulk deposition along its flanks. The volcanic plume consists of solid particles, acidic droplets and gaseous species. After H2O and CO2, S, Cl and F represent the most abundant volatile elements emitted as gaseous species from the craters. During rain events acidic gases interact rapidly with droplets lowering the pH of rain. This process favors the dissolution and dissociation of the most acidic gases. Under these conditions, the chemical weathering of volcanic rocks and ashes is promoted by the acid rain during its infiltration. Subsequently during groundwater circulation, chemical weathering of volcanic rocks is also driven by the huge amount of deep magmatic carbon dioxide (CO2) coming up through the volcanic edifice and dissolving in the water. These two different weathering steps occur under very different conditions. The former occurs in a highly acidic environment (pH < 4) and the reaction rates depend strongly on the pH, while the latter usually occurs under slightly acidic conditions since the pH has been already neutralized by the interaction with volcanics rocks. The high content of chlorine is mainly derived from interactions between the plume and rainwater, while the total alkalinity can be completely ascribed to the dissociation of carbonic acid (H2CO3) after the hydration of CO2. The relative contributions of plume-derived elements/weathering and CO2-driven weathering has been computed for each element. In addition, the comparison between the chemical compositions of the bulk deposition and of groundwater provides a new understanding about the mobility of volatile elements. Other processes such as ion exchange, iddingsite formation, and carbonate precipitation can also play roles, but only to minor extents. The proposed approach has revealed that the persistent plume strongly affects the chemical composition of groundwater at Mt. Etna and probably also at other volcanoes characterized by huge open-conduit degassing activity.
U.S. Geological Survey Karst Interest Group Proceedings, Bowling Green, Kentucky, May 27-29, 2008

USGS Publications Warehouse

Kuniansky, Eve L.

2008-01-01

*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
Carbon Nanomaterials for Detection, Assessment and Purification of Oil and Natural Gas

NASA Astrophysics Data System (ADS)

Hwang, Chih-Chau

This thesis studies several carbon nanomaterials. Their synthesis and characterization are studied as well as their potential applications to the oil industry. The carbon nanomaterials studied here include mesoporous carbon (CMK-3), sulfur- or nitrogen-doped porous carbon (SPC or NPC), and commercial carbon black (CB). Through appropriate functionalization, these carbon nanomaterials exhibit unique properties and their performances in detection, assessment as well as purification of oil and natural gas are studied and demonstrated. First, it was shown that amine-modified CMK-3 composites, polyethylenimine-CMK-3 (PEI-CMK-3) and polyvinylamine-CMK-3 (PVA-CMK-3) can be synthesized through in situ polymerization of amine species within the channels of the CMK-3. The synthesis process results in the entrapped amine polymers interpenetrating the composite frameworks of the CMK-3, improving the CO2 capture performance and recycle stability. CO2 uptake by the synthesized composites was determined using a gravimetric method at 30°C and 1 atm; the 39% PEI-CMK-3 composite had ˜12 wt% (3.1 mmol/g) CO2 uptake capacity and the 37% PVA-CMK-3 composite had ˜13 wt% (3.5 mmol/g) CO 2 uptake capacity. A desorption temperature of 75°C was sufficient for regeneration. The CO2 uptake was the same when using 10% CO 2 in a 90% CH4, C2H6 and C3H 8 mixture, underscoring this composite's efficacy for CO 2 sequestration from natural gas. Secondly, nucleophilic porous carbons (SPC and NPC) were synthesized from simple and inexpensive carbon-sulfur and carbon-nitrogen precursors. A strong sorbate-sorbent interaction between CO2 and nucleophilic centers in the porous carbon was established using spectroscopic and heat of sorption data. Raman spectroscopy supports the assertion that the nucleophilic centers react with the CO2 to produce carbonate anions that further cause polymerization in the porous carbon channels to form poly(CO2) under much lower pressure than previously reported for such polymer formation. Once returned to ambient conditions, the poly(CO2) depolymerizes during the pressure swing, leading to a sorbent that can be easily regenerated without the thermal energy input that is required for traditional liquid phase sorbents. The synergy between the nucleophilic centers and the high surface area porous carbon produces a sorbent with high CO2 capacity, selectivity, and volumetric efficiency, so that the materials have potential to be used for CO2 removal from natural gas streams. As energy demand continues to increase, it is desirable to produce as much oil as possible from existing oil wells. Tracers have long been used to map entry/exit well correlations in the oil-field, but they do not provide any information about the environment between the entry and exit locations. Hence, the third part of this thesis will show that nanoparticles possessing functionalized carbon black (fCB) cores and sulfated polyvinyl alcohol (sPVA) addends can be designed to transport hydrocarbon detection molecules through subsurface rock formations. The sPVA-fCBs are stable under high-temperature and salinity conditions and are transported through a variety of oilfield rock types. A non-radioactive probe molecule that is easily detectable by mass spectrometry, triheptylamine (THA), was adsorbed onto the sPVA-fCBs. The THA was selectively released when the nanoparticles were passed through a column of isooctane-containing crushed rock, providing a path to both entry and exit correlations and a measure of oil content. This study simulates detection and quantitative analysis of the hydrocarbon content in downhole rock formations, which is a critically needed assessment in older oilfields. Crude oil is classified as "sour" when it contains a total sulfur content greater than 0.5%. Among these sulfur species, H2S is the one of main impurities in sour crude. The sour crude is toxic and corrosive to the materials of construction in pipelines and other holding and transportation vessels. Since the sulfur amount in a sample of crude depends on where it was found, if the concentration of the sulfur species in the subsurface could be accurately monitored, then geologists might be able to evaluate the quality of the crude before large scale extraction ensues. The last part of the thesis covers polyvinyl alcohol functionalized carbon black (PVA-CB). The particles have high stability under high temperature and salinity conditions, and they acts as a carrier to transport molecular cargo efficiently through simulated oilfield formations. After being functionalized with H2S-sensitive moieties, the functionalized PVA-CB can be pumped through H2S-containing oil and water in porous rock and the H2S content can be determined based on the fluorescent enhancement of the H2S-sensitive addends.
Graphite as a Biomarker in Rocks of the 3.8 Ga Isua Supracrustal Belt

NASA Astrophysics Data System (ADS)

Lepland, A.; van Zuilen, M.; Layne, G. D.; Arrhenius, G.

2002-12-01

Recent petrographic and isotopic studies of graphite and apatite in supracrustal rocks from the 3.8 Ga Isua belt (ISB) in southern West Greenland [1, 2] have shown inconsistencies in interpreting traces of life in the earliest terrestrial sediment record. Isotopically light graphitic carbon, suggestive of a bioorganic origin, has been previously reported from the carbonate-rich Isua rocks [3, 4] that at the time were recognized as sedimentary deposits. However, these carbonate-rich rocks, that provided the basis for original biologic interpretations, have been shown to have a metasomatic origin [5] not sedimentary as previously believed. This protolith reinterpretation has highlighted the need for assessment of graphite genesis and related isotopic systematics when using graphite as an ancient biomarker. We have, for this purpose, studied graphite in a suite of samples from the ISB including metacarbonates, turbidites, cherts and banded iron formations (BIFs). Graphite is relatively abundant (0.1-2 wt. %) in metacarbonate samples, while the abundances of reduced carbon in metasedimentary BIFs and metacherts are below 100 ppm. Petrographic analyses show that graphite in metacarbonates typically associates with Fe-bearing carbonate and magnetite. This mineral association indicates graphite formation in Isua metacarbonates by thermal-metamorphic reduction of carbonate ion, in which the carbonate ion is reduced to form graphite and ferrous iron is oxidized to form magnetite. Carbon isotopic compositions of graphite (δ13C ca. -2 per mil) and associated Fe-carbonate (δ13C ca. -6 per mil) indicate isotopic equilibrium between these two phases at ca. 500 C, consistent with the metamorphic history of the ISB. Stepped-combustion experiments undertaken on Isua BIFs and metacherts reveal that these sediments contain virtually no graphite, and the small amount of reduced carbon found there represents recent organic contamination. Our stepped-combustion-mass-spectrometry data demonstrate that previous isotopic results on graphite deficient Isua rocks obtained by single step combustion are unreliable. The proposed biologic significance of graphite occurring as inclusions in apatite [4] in Isua rocks is not supported by our findings because such graphite-apatite association can only be found in biologically irrelevant metacarbonate rocks. The isotopic systematics of the epigenetic processes responsible for formation of isotopically light graphite enclosed in apatite crystals [4] will be discussed, integrating new ion microprobe isotope data on graphite in apatite and other mineral phases occurring in Isua metacarbonates. References: [1] van Zuilen, M., Lepland, A. and Arrhenius, G., 2002. Reassessing the evidence for the earliest traces of life. Nature 418: 627-630. [2] Lepland, A., Arrhenius, G. and Cornell, D. in press. Apatite in early Archean Isua supracrustal rocks, southern West Greenland: its origin, association with graphite and potential as a biomarker. Precam. Res. [3] Schidlowski, M., 1988. A 3,800-million-year isotopic record of life from carbon in sedimentary rocks. Nature 333: 313-318. [4] Mojzsis, S.J., Arrhenius, G., McKeegan, K.D., Harrison, T.M., Nutman, A.P. and Friend, C.R.L., 1996. Evidence for life on Earth before 3800 million years ago. Nature 384: 55-59. [5] Rosing, M.T., Rose, N.M., Bridgwater, D. and Thomsen, H.S., 1996. Earliest part of Earth's stratigraphic record: a reappraisal of the >3.7 Ga Isua (Greenland) supracrustal sequence. Geol. 24: 43-46.
Silicate Carbonation in Supercritical CO2 Containing Dissolved H2O: An in situ High Pressure X-Ray Diffraction Study

DOE Office of Scientific and Technical Information (OSTI.GOV)

Schaef, Herbert T.; Miller, Quin RS; Thompson, Christopher J.

2013-06-30

Technological advances have been significant in recent years for managing environmentally harmful emissions (mostly CO2) resulting from combustion of fossil fuels. Deep underground geologic formations are emerging as reasonable options for long term storage of CO2 but mechanisms controlling rock and mineral stability in contact with injected supercritical fluids containing water are relatively unknown. In this paper, we discuss mineral transformation reactions occurring between supercritical CO2 containing water and the silicate minerals forsterite (Mg2SiO4), wollastonite (CaSiO3), and enstatite (MgSiO3). This study utilizes newly developed in situ high pressure x-ray diffraction (HXRD) and in situ infra red (IR) to examine mineralmore » transformation reactions. Forsterite and enstatite were selected as they are important minerals present in igneous and mafic rocks and have been the subject of a large number of aqueous dissolution studies that can be compared with non-aqueous fluid tests in this study. Wollastonite, classified as a pyroxenoid (similar to a pyroxene), was chosen as a suitably fast reacting proxy for examining silicate carbonation processes associated with a wet scCO2 fluid as related to geologic carbon sequestration. The experiments were conducted under modest pressures (90 to 160 bar), temperatures between 35° to 70° C, and varying concentrations of dissolved water. Under these conditions scCO2 contains up to 3,500 ppm dissolved water.« less
Dynamics of metasomatic transformation of lithospheric mantle rocks under Siberian Craton

NASA Astrophysics Data System (ADS)

Sharapov, Victor; Perepechko, Yury; Tomilenko, Anatoly; Chudnenko, Konstantin; Sorokin, Konstantin

2014-05-01

Numerical problem for one- and two-velocity hydrodynamics of heat and mass transfer in permeable zones over 'asthenospheric lenses' (with estimates for dynamics of non-isothermal metasomatosis of mantle rocks, using the approximation of flow reactor scheme) was formulated and solved based on the study of inclusion contents in minerals of metamorphic rocks of the lithosphere mantle and earth crust, estimates of thermodynamic conditions of inclusions appearance, and the results of experimental modeling of influence of hot reduced gases on rocks and minerals of xenoliths in mantle rocks under the cratons of Siberian Platform (SP): 1) the supply of fluid flows of any composition from upper mantle magma sources results in formation of zonal metasomatic columns in ultrabasic lithosphere mantle in permeable zones of deep faults; 2) when major element or petrogenetic components are supplied from magma source, depleted ultrabasic rocks of the lithosphere mantle are transformed into substrates which can be regarded as deep analogs of crust rodingites; 3) other fluid compositions cause deep calcinations and noticeable salination of metasomated substrate, or garnetization (eclogitization) of primary ultrabasic matrix develops; 4) above these zones the zone of basification appears; it is changed by the area of pyroxenitization, amphibolization, and biotitization; 5) modeling of thermo and mass exchange for two-velocity hydrodynamic problem showed that hydraulic approximation increases velocities of heat front during convective heating and decreases pressure in fluid along the flow. It was shown that grospydites, regarded earlier as eclogites, in permeable areas of lithosphere mantle, are typical zones draining upper mantle magma sources of metasomatic columns. As a result of the convective melting the polybaric magmatic sources may appear. Thus the formation of the (kimberlites?) melilitites or carbonatites is possible at the base of the lithospheric plates. It is shown that the physico - chemical conditions of the carbonation of the depleted mantle peridotites refer to the narrow interval of the possible fluid compositions. The bulk fluid content near 4 weight % with the SiO2 CaO 0.5 - 0.1 molar volumes the 1) the Si/Ca molar ratio is < 1; 2) in the C-H-O system the molar ration should be 1/2/3 - 2/1/2; 3) the pO2 variations should be -8 < lg pO2 < -11; 4) in the fluid the CO2 content is twice higher than H2O and Cl essentially prevail under F. In the system with smaller fraction of the fluid phase less increased by the major element rock components the carbonation is more intensive when the Ca content decrease. The fusions of the basic magmas are possible within the wehrlitization zones. The work is supported by RFBR grant 12-05-00625.
Hydrogeologic framework of the Floridan aquifer system in Florida and in parts of Georgia, South Carolina, and Alabama

USGS Publications Warehouse

Miller, James A.

1986-01-01

The Floridan aquifer system of the Southeastern United States is comprised of a thick sequence of carbonate rocks that are mostly of Paleocene to early Miocene age and that are hydraulically connected in varying degrees. The aquifer system consists of a single vertically continuous permeable unit updip and of two major permeable zones (the Upper and Lower Floridan aquifers) separated by one of seven middle confining units downdip. Neither the boundaries of the aquifer system or of its component high- and low-permeability zones necessarily conform to either formation boundaries or time-stratigraphic breaks. The rocks that make up the Floridan aquifer system, its upper and lower confining units, and a surficial aquifer have been separated into several chronostratigraphic units. The external and internal geometry of these stratigraphic units is presented on a series of structure contour and isopach maps and by a series of geohydrologic cross sections and a fence diagram. Paleocene through middle Eocene units consist of an updip clastic facies and a downdip carbonate bank facies, that extends progressively farther north and east in progressively younger units. Upper Eocene and Oligocene strata are predominantly carbonate rocks throughout the study area. Miocene and younger strata are mostly clastic rocks. Subsurface data show that some modifications in current stratigraphic nomenclature are necessary. First, the middle Eocene Lake City Limestone cannot be distinguished lithologically or faunally from the overlying middle Eocene Avon Park 'Limestone.' Accordingly, it is proposed that the term Lake City be abandoned and the term Avon Park Formation be applied to the entire middle Eocene carbonate section of peninsular Florida and southeastern Georgia. A reference well section in Levy County, Fla., is proposed for the expanded Avon Park Formation. The Avon Park is called a 'formation' more properly than a 'limestone' because the unit contains rock types other than limestone. Second, like the Avon Park, the lower Eocene Oldsmar and Paleocene Cedar Keys 'Limestones' of peninsular Florida practically everywhere contain rock types other than limestone. It is therefore proposed that these units be referred to more accurately as Oldsmar Formation and Cedar Keys Formation. The uppermost hydrologic unit in the study area is a surficial aquifer that can be divided into (1) a fluvial sand-and-gravel aquifer in southwestern Alabama and westernmost panhandle Florida, (2) limestone and sandy limestone of the Biscayne aquifer in southeastern peninsular Florida, and (3) a thin blanket of terrace and fluvial sands elsewhere. The surficial aquifer is underlain by a thick sequence of fine clastic rocks and low-permeability carbonate rocks, most of which are part of the middle Miocene Hawthorn Formation and all of which form the upper confining unit of the Floridan aquifer system. In places, the upper confining unit has been removed by erosion or is breached by sinkholes. Water in the Floridan aquifer system thus occurs under unconfined, semiconfined, or fully confined conditions, depending upon the presence, thickness, and integrity of the upper confining unit. Within the Floridan aquifer system, seven low permeability zones of subregional extent split the aquifer system in most places into an Upper and Lower Floridan aquifer. The Upper Floridan aquifer, which consists of all or parts of rocks of Oligocene age, late Eocene age, and the upper half of rocks of middle Eocene age, is highly permeable. The middle confining units that underlie the Upper Floridan are mostly of middle Eocene age but may be as young as Oligocene or as old as early Eocene. Where no middle confining unit exists, the entire aquifer system is comprised of permeable rocks and for hydrologic discussions is treated as the Upper Floridan aquifer. The Lower Floridan aquifer contains a cavernous high-permeability horizon in the lower part of the early Eocene of south
Geologic map of the White Hall quadrangle, Frederick County, Virginia, and Berkeley County, West Virginia

USGS Publications Warehouse

Doctor, Daniel H.; Orndorff, Randall C.; Parker, Ronald A.; Weary, David J.; Repetski, John E.

2010-01-01

The White Hall 7.5-minute quadrangle is located within the Valley and Ridge province of northern Virginia and the eastern panhandle of West Virginia. The quadrangle is one of several being mapped to investigate the geologic framework and groundwater resources of Frederick County, Va., as well as other areas in the northern Shenandoah Valley of Virginia and West Virginia. All exposed bedrock outcrops are clastic and carbonate strata of Paleozoic age ranging from Middle Cambrian to Late Devonian. Surficial materials include unconsolidated alluvium, colluvium, and terrace deposits of Quaternary age, and local paleo-terrace deposits possibly of Tertiary age. The quadrangle lies across the northeast plunge of the Great North Mountain anticlinorium and includes several other regional folds. The North Mountain fault zone cuts through the eastern part of the quadrangle; it is a series of thrust faults generally oriented northeast-southwest that separate the Silurian and Devonian clastic rocks from the Cambrian and Ordovician carbonate rocks and shales. Karst development in the quadrangle occurs in all of the carbonate rocks. Springs occur mainly near or on faults. Sinkholes occur within all of the carbonate rock units, especially where the rocks have undergone locally intensified deformation through folding, faulting, or some combination.
Nanodiamond finding in the hyblean shallow mantle xenoliths.

PubMed

Simakov, S K; Kouchi, A; Mel'nik, N N; Scribano, V; Kimura, Y; Hama, T; Suzuki, N; Saito, H; Yoshizawa, T

2015-06-01

Most of Earth's diamonds are connected with deep-seated mantle rocks; however, in recent years, μm-sized diamonds have been found in shallower metamorphic rocks, and the process of shallow-seated diamond formation has become a hotly debated topic. Nanodiamonds occur mainly in chondrite meteorites associated with organic matter and water. They can be synthesized in the stability field of graphite from organic compounds under hydrothermal conditions. Similar physicochemical conditions occur in serpentinite-hosted hydrothermal systems. Herein, we report the first finding of nanodiamonds, primarily of 6 and 10 nm, in Hyblean asphaltene-bearing serpentinite xenoliths (Sicily, Italy). The discovery was made by electron microscopy observations coupled with Raman spectroscopy analyses. The finding reveals new aspects of carbon speciation and diamond formation in shallow crustal settings. Nanodiamonds can grow during the hydrothermal alteration of ultramafic rocks, as well as during the lithogenesis of sediments bearing organic matter.
Carbonation of subduction-zone serpentinite (high-pressure ophicarbonate; Ligurian Western Alps) and implications for the deep carbon cycling

NASA Astrophysics Data System (ADS)

Scambelluri, Marco; Bebout, Gray E.; Belmonte, Donato; Gilio, Mattia; Campomenosi, Nicola; Collins, Nathan; Crispini, Laura

2016-05-01

Much of the long-term carbon cycle in solid earth occurs in subduction zones, where processes of devolatilization, partial melting of carbonated rocks, and dissolution of carbonate minerals lead to the return of CO2 to the atmosphere via volcanic degassing. Release of COH fluids from hydrous and carbonate minerals influences C recycling and magmatism at subduction zones. Contradictory interpretations exist regarding the retention/storage of C in subducting plates and in the forearc to subarc mantle. Several lines of evidence indicate mobility of C, of uncertain magnitude, in forearcs. A poorly constrained fraction of the 40-115 Mt/yr of C initially subducted is released into fluids (by decarbonation and/or carbonate dissolution) and 18-43 Mt/yr is returned at arc volcanoes. Current estimates suggest the amount of C released into subduction fluids is greater than that degassed at arc volcanoes: the imbalance could reflect C subduction into the deeper mantle, beyond subarc regions, or storage of C in forearc/subarc reservoirs. We examine the fate of C in plate-interface ultramafic rocks, and by analogy serpentinized mantle wedge, via study of fluid-rock evolution of marble and variably carbonated serpentinite in the Ligurian Alps. Based on petrography, major and trace element concentrations, and carbonate C and O isotope compositions, we demonstrate that serpentinite dehydration at 2-2.5 GPa, 550 °C released aqueous fluids triggering breakdown of dolomite in nearby marbles, thus releasing C into fluids. Carbonate + olivine veins document flow of COH fluids and that the interaction of these COH fluids with serpentinite led to the formation of high-P carbonated ultramafic-rock domains (high-P ophicarbonates). We estimate that this could result in the retention of ∼0.5-2.0 Mt C/yr in such rocks along subduction interfaces. As another means of C storage, 1 to 3 km-thick layers of serpentinized forearc mantle wedge containing 50 modal % dolomite could sequester 1.62 to 4.85 Mt C/yr. We stress that lithologically complex interfaces could contain sites of both C release and C addition, further confounding estimates of net C loss at forearc and subarc depths. Sites of C retention, also including carbonate veins and graphite as reduced carbonate, could influence the transfer of slab C to at least the depths beneath volcanic fronts.
Attenuation and Dispersion Analysis in Laboratory Measured Elastic Properties in the Middle East Carbonate Reservoir Rocks

NASA Astrophysics Data System (ADS)

Sharma, R.

2016-12-01

Carbonate rocks are sensitive to circulation of fluid types that leads to diagenetic alterations and therefore to heterogeneity in distribution of porosity and permeability. These heterogeneities in turn, lead to heterogeneity in saturations varying from partial to patchy to uniform. Depending on the interaction between fluids and rock matrix, a weakening or strengthening in shear modulus of carbonate rocks can also develop (Eberli et al., 2003; Adam et al., 2006; Sharma et al., 2009; Sharma et al., 2013). Thus the elastic response over the production life of the carbonate reservoirs can change considerably. Efforts to couple fluid flow with varying seismic properties of these reservoirs are limited in success due to the differences between static elastic properties derived from reservoir simulation and dynamic elastic properties derived from inverted seismic. An additional limitation arises from the assumption that shear modulus does not change with fluid type and saturations. To overcome these limitations, we need to understand the relationships between the static and the dynamic elastic properties using laboratory measurements made at varying pressures, frequencies and with varying saturants. I will present the following results: 1) errors associated with using dynamic (2 - 2000 Hz and 1 MHz) elastic properties data for static ( 0 Hz) reservoir properties, 2) shear modulus variation in carbonates upon saturation with varying saturants The results will enable us to estimate, 1) distribution of stress-strain relations in reservoir rocks and 2) modulus dispersion to correct seismic-derived moduli as inputs for reservoir simulators. The results are critical to estimate, 1) modulus dispersion correction and 2) occurrence and amount of shear modulus variation with fluid change vital for rock stability analysis
Origin and migration of hydrocarbon gases and carbon dioxide, Bekes Basin, southeastern Hungary

USGS Publications Warehouse

Clayton, J.L.; Spencer, C.W.; Koncz, I.; Szalay, A.

1990-01-01

The Bekes Basin is a sub-basin within the Pannonian Basin, containing about 7000 m of post-Cretaceous sedimentary rocks. Natural gases are produced from reservoirs (Precambrian to Tertiary in age) located on structural highs around the margins of the basin. Gas composition and stable carbon isotopic data indicate that most of the flammable gases were derived from humic kerogen contained in source rocks located in the deep basin. The depth of gas generation and vertical migration distances were estimated using quantitative source rock maturity-carbon isotope relationships for methane compared to known Neogene source rock maturity-depth relationships in the basin. These calculations indicate that as much as 3500 m of vertical migration has occured in some cases. Isotopically heavy (> - 7 > 0) CO2 is the predominant species present in some shallow reservoirs located on basin-margin structural highs and has probably been derived via long-distance vertical and lateral migration from thermal decompositon of carbonate minerals in Mesozoic and older rocks in the deepest parts of the basin. A few shallow reservoirs (< 2000m) contain isotopically light (-50 to -60%0) methane with only minor amounts of C2+ homologs (< 3% v/v). This methane is probably mostly microbial in origin. Above-normal pressures, occuring at depths greater than 1800 m, are believed to be the principal driving force for lateral and vertical gas migration. These pressures are caused in part by active hydrocarbon generation, undercompaction, and thermal decomposition of carbonates.

Effect of chemical environment and rock composition on fracture mechanics properties of reservoir lithologies in context of CO2 sequestration

NASA Astrophysics Data System (ADS)

Major, J. R.; Eichhubl, P.; Callahan, O. A.

2015-12-01

The coupled chemical and mechanical response of reservoir and seal rocks to injection of CO2 have major implications on the short and long term security of sequestered carbon. Many current numerical models evaluating behavior of reservoirs and seals during and after CO2 injection in the subsurface consider chemistry and mechanics separately and use only simple mechanical stability criteria while ignoring time-dependent failure parameters. CO2 injection irreversibly alters the subsurface chemical environment which can then affect geomechanical properties on a range of time scales by altering rock mineralogy and cements through dissolution, remobilization, and precipitation. It has also been documented that geomechanical parameters such as fracture toughness (KIC) and subcritical index (SCI) are sensitive to chemical environment. Double torsion fracture mechanics testing of reservoir lithologies under controlled environmental conditions relevant to CO2 sequestration show that chemical environment can measurably affect KIC and SCI. This coupled chemical-mechanical behavior is also influenced by rock composition, grains, amount and types of cement, and fabric. Fracture mechanics testing of the Aztec Sandstone, a largely silica-cemented, subarkose sandstone demonstrate it is less sensitive to chemical environment than Entrada Sandstone, a silty, clay-rich sandstone. The presence of de-ionized water lowers KIC by approximately 20% and SCI 30% in the Aztec Sandstone relative to tests performed in air, whereas the Entrada Sandstone shows reductions on the order of 70% and 90%, respectively. These results indicate that rock composition influences the chemical-mechanical response to deformation, and that the relative chemical reactivity of target reservoirs should be recognized in context of CO2 sequestration. In general, inert grains and cements such as quartz will be less sensitive to the changing subsurface environment than carbonates and clays.
Use of nanotomographic images for structure analysis of carbonate rocks

DOE Office of Scientific and Technical Information (OSTI.GOV)

Nagata, Rodrigo; Appoloni, Carlos Roberto

Carbonate rocks store more than 50% of world's petroleum. These rocks' structures are highly complex and vary depending on many factors regarding their formation, e.g., lithification and diagenesis. In order to perform an effective extraction of petroleum it is necessary to know petrophysical parameters, such as total porosity, pore size and permeability of the reservoir rocks. Carbonate rocks usually have a range of pore sizes that goes from nanometers to meters or even dozen of meters. The nanopores and micropores might play an important role in the pores connectivity of carbonate rocks. X-ray computed tomography (CT) has been widely usedmore » to analyze petrophysical parameters in recent years. This technique has the capability to generate 2D images of the samples' inner structure and also allows the 3D reconstruction of the actual analyzed volume. CT is a powerful technique, but its results depend on the spatial resolution of the generated image. Spatial resolution is a measurement parameter that indicates the smallest object that can be detected. There are great difficulties to generate images with nanoscale resolution (nanotomographic images). In this work three carbonate rocks, one dolomite and two limestones (that will be called limestone A and limestone B) were analyzed by nanotomography. The measurements were performed with the SkyScan2011 nanotomograph, operated at 60 kV and 200 μA to measure the dolomite sample and 40 kV and 200 μA to measure the limestone samples. Each sample was measured with a given spatial resolution (270 nm for the dolomite sample, 360 nm for limestone A and 450 nm for limestone B). The achieved results for total porosity were: 3.09 % for dolomite, 0.65% for limestone A and 3.74% for limestone B. This paper reports the difficulties to acquire nanotomographic images and further analysis about the samples' pore sizes.« less
Quantification of CO2-FLUID-ROCK Reactions Using Reactive and Non-Reactive Tracers

NASA Astrophysics Data System (ADS)

Matter, J.; Stute, M.; Hall, J. L.; Mesfin, K. G.; Gislason, S. R.; Oelkers, E. H.; Sigfússon, B.; Gunnarsson, I.; Aradottir, E. S.; Alfredsson, H. A.; Gunnlaugsson, E.; Broecker, W. S.

2013-12-01

Carbon dioxide mineralization via fluid-rock reactions provides the most effective and long-term storage option for geologic carbon storage. Injection of CO2 in geologic formations induces CO2 -fluid-rock reactions that may enhance or decrease the storage permanence and thus the long-term safety of geologic carbon storage. Hence, quantitative characterization of critical CO2 -fluid-rock interactions is essential to assess the storage efficiency and safety of geologic carbon storage. In an attempt to quantify in-situ fluid-rock reactions and CO2 transport relevant for geologic carbon storage, we are testing reactive (14C, 13C) and non-reactive (sodium fluorescein, amidorhodamine G, SF5CF3, and SF6) tracers in an ongoing CO2 injection in a basaltic storage reservoir at the CARBFIX pilot injection site in Iceland. At the injection site, CO2 is dissolved in groundwater and injected into a permeable basalt formation located 500-800 m below the surface [1]. The injected CO2 is labeled with 14C by dynamically adding calibrated amounts of H14CO3-solution into the injection stream in addition to the non-reactive tracers. Chemical and isotopic analyses of fluid samples collected in a monitoring well, reveal fast fluid-rock reactions. Maximum SF6 concentration in the monitoring well indicates the bulk arrival of the injected CO2 solution but dissolved inorganic carbon (DIC) concentration and pH values close to background, and a potentially lower 14C to SF6 ratio than the injection ratio suggest that most of the injected CO2 has reacted with the basaltic rocks. This is supported by δ13CDIC, which shows a drop from values close to the δ 13C of the injected CO2 gas (-3‰ VPDB) during breakthrough of the CO2 plume to subsequent more depleted values (-11.25‰ VPDB), indicating precipitation of carbonate minerals. Preliminary mass balance calculations using mixing relationships between the background water in the storage formation and the injected solution, suggest that approximately 85% of the injected CO2 must have reacted along the flow path from the injection well to the monitoring well within less than one year. Monitoring is still going on and we will extend the time series and the mass balance accordingly. Our study demonstrates that by combining reactive and non-reactive tracers, we are able to quantify CO2-fluid-rock interactions on a reservoir scale. [1] Gislason et al. (2010), Int. J. Greenh. Gas Con. 4, 537-545.
Geophysical delineation of Mg-rich ultramafic rocks for mineral carbon sequestration

USGS Publications Warehouse

McCafferty, Anne E.; Van Gosen, Bradley S.; Krevor, Sam C.; Graves, Chris R.

2009-01-01

This presentation covers three general topics: (1) description of a new geologic compilation of the United States that shows the location of magnesium-rich ultramafic rocks in the conterminous United States; (2) conceptual illustration of the potential ways that ultramafic rocks could be used to sequester carbon dioxide; and (3) description of ways to use geophysical data to refine and extend the geologic mapping of ultramafic rocks and to better characterize their mineralogy.The geophysical focus of this research is twofold. First, we illustrate how airborne magnetic data can be used to map the shallow subsurface geometry of ultramafic rocks for the purpose of estimating the volume of rock material available for mineral CO2 sequestration. Secondly, we explore, on a regional to outcrop scale, how magnetic mineralogy, as expressed in magnetic anomalies, may vary with magnesium minerals, which are the primary minerals of interest for CO2 sequestration.
Titrimetric Determination of Carbon Dioxide in a Heterogeneous Sample ("Pop Rocks")

NASA Astrophysics Data System (ADS)

Davis, Craig M.; Mauck, Matthew C.

2003-05-01

A traditional exercise in quantitative analysis is the titration of mixtures of sodium hydroxide, sodium carbonate, and sodium bicarbonate. Often, consumer products are studied. A procedure to analyze the total volume of carbon dioxide bubbles in the candy "Pop Rocks" is presented. The popularity of the sample and the simplicity of the procedure make this exercise suitable for a wide variety of students: from non-science majors to chemistry majors in a quantitative analysis course.
Petroleum geology and resources of the North Ustyurt Basin, Kazakhstan and Uzbekistan

USGS Publications Warehouse

Ulmishek, Gregory F.

2001-01-01

The triangular-shaped North Ustyurt basin is located between the Caspian Sea and the Aral Lake in Kazakhstan and Uzbekistan and extends offshore both on the west and east. Along all its sides, the basin is bounded by the late Paleozoic and Triassic foldbelts that are partially overlain by Jurassic and younger rocks. The basin formed on a cratonic microcontinental block that was accreted northward to the Russian craton in Visean or Early Permian time. Continental collision and deformation along the southern and eastern basin margins occurred in Early Permian time. In Late Triassic time, the basin was subjected to strong compression that resulted in intrabasinal thrusting and faulting. Jurassic-Tertiary, mostly clastic rocks several hundred meters to 5 km thick overlie an older sequence of Devonian?Middle Carboniferous carbonates, Upper Precambrian massifs and deformed Caledonian foldbelts. The Carboniferous?Lower Permian clastics, carbonates, and volca-basement is at depths from 5.5 km on the highest uplifts to 11 nics, and Upper Permian?Triassic continental clastic rocks, pri-km in the deepest depressions. marily red beds. Paleogeographic conditions of sedimentation, Three total petroleum systems are identified in the basin. the distribution of rock types, and the thicknesses of pre-Triassic Combined volumes of discovered hydrocarbons in these sysstratigraphic units are poorly known because the rocks have been tems are nearly 2.4 billion barrels of oil and 2.4 trillion cubic penetrated by only a few wells in the western and eastern basin feet of gas. Almost all of the oil reserves are in the Buzachi Arch areas. The basement probably is heterogeneous; it includes and Surrounding Areas Composite Total Petroleum System in 2 Petroleum Geology, Resources?North Ustyurt Basin, Kazakhstan and Uzbekistan the western part of the basin. Oil pools are in shallow Jurassic and Neocomian sandstone reservoirs, in structural traps. Source rocks are absent in the total petroleum system area; therefore, the oil could have migrated from the adjacent North Caspian basin. The North Ustyurt Jurassic Total Petroleum System encompasses the rest of the basin area and includes Jurassic and younger rocks. Several oil and gas fields have been discovered in this total petroleum system. Oil accumulations are in Jurassic clastic reservoirs, in structural traps at depths of 2.5?3 km. Source rocks for the oil are lacustrine beds and coals in the continental Jurassic sequence. Gas fields are in shallow Eocene sandstones in the northern part of the total petroleum system. The origin of the gas is unknown. The North Ustyurt Paleozoic Total Petroleum System stratigraphically underlies the North Ustyurt Jurassic system and occupies the same geographic area. The total petroleum system is almost unexplored. Two commercial flows of gas and several oil and gas shows have been tested in Carboniferous shelf carbonates in the eastern part of the total petroleum system. Source rocks probably are adjacent Carboniferous deep-water facies interpreted from seismic data. The western extent of the total petroleum system is conjectural. Almost all exploration drilling in the North Ustyurt basin has been limited to Jurassic and younger targets. The underlying Paleozoic-Triassic sequence is poorly known and completely unexplored. No wells have been drilled in offshore parts of the basin. Each of three total petroleum systems was assessed as a single assessment unit. Undiscovered resources of the basin are small to moderate. Most of the undiscovered oil probably will be discovered in Jurassic and Neocomian stratigraphic and structural traps on the Buzachi arch, especially on its undrilled off-shore extension. Most of the gas discoveries are expected to be in Paleozoic carbonate reservoirs in the eastern part of the basin.
Geological and geomechanical properties of the carbonate rocks at the eastern Black Sea Region (NE Turkey)

NASA Astrophysics Data System (ADS)

Ersoy, Hakan; Yalçinalp, Bülent; Arslan, Mehmet; Babacan, Ali Erden; Çetiner, Gözde

2016-11-01

Turkey located in the Alpine-Himalayan Mountain Belt has 35% of the natural stone reserves of the world and has good quality marble, limestone, travertine and onyx reserves especially in the western regions of the country. The eastern Black Sea Region with a 1.4 million meters cubes reserve has a little role on the natural stone production in the country. For this reason, this paper deals with investigation on the potential of carbonate stone in the region and determination of the geological and geo-mechanical properties of these rocks in order to provide economic contribution to the national economy. While the study sites are selected among the all carbonate rock sites, the importance as well as the representative of the sites were carefully considered for the region. After representative samples were analyzed for major oxide and trace element compositions to find out petrochemical variations, the experimental program conducted on rock samples for determination of both physical and strength properties of the carbonate rocks. The results of the tests showed that there are significant variations in the geo-mechanical properties of the studied rock groups. The density values vary from 2.48 to 2.70 gr/cm3, water absorption by weight values range from 0.07 to 1.15% and the apparent porosity of the carbonate rocks are between 0.19 and 3.29%. However, the values of the UCS shows variation from 36 to 80 MPa. Tensile and bending strength values range from 3.2 to 7.5 MPa and 6.0-9.2 MPa respectively. Although the onyx samples have the lowest values of apparent porosity and water absorption by weight, these samples do not have the highest values of UCS values owing to occurrence of the micro-cracks. The UCS values of the rock samples were also found after cycling tests However, the limestone samples have less than 5% deterioration after freezing-thawing and wetting-drying tests, but travertine and onyx samples have more than 15% deterioration. Exception of the apparent porosity values of travertine samples, all geo-mechanical properties of the studied carbonate rocks were determined in the acceptance values given by Turkish Standards Institute (TSE) for using as a natural dimension stone. After these investigations, it is anticipated that in the near future the number of quarries and factories will increase and more types of natural stones will be discovered in the eastern Black Sea Region and thus this will provide economic contribution to the economy of the country.
Evidence for early life in Earth's oldest hydrothermal vent precipitates.

PubMed

Dodd, Matthew S; Papineau, Dominic; Grenne, Tor; Slack, John F; Rittner, Martin; Pirajno, Franco; O'Neil, Jonathan; Little, Crispin T S

2017-03-01

Although it is not known when or where life on Earth began, some of the earliest habitable environments may have been submarine-hydrothermal vents. Here we describe putative fossilized microorganisms that are at least 3,770 million and possibly 4,280 million years old in ferruginous sedimentary rocks, interpreted as seafloor-hydrothermal vent-related precipitates, from the Nuvvuagittuq belt in Quebec, Canada. These structures occur as micrometre-scale haematite tubes and filaments with morphologies and mineral assemblages similar to those of filamentous microorganisms from modern hydrothermal vent precipitates and analogous microfossils in younger rocks. The Nuvvuagittuq rocks contain isotopically light carbon in carbonate and carbonaceous material, which occurs as graphitic inclusions in diagenetic carbonate rosettes, apatite blades intergrown among carbonate rosettes and magnetite-haematite granules, and is associated with carbonate in direct contact with the putative microfossils. Collectively, these observations are consistent with an oxidized biomass and provide evidence for biological activity in submarine-hydrothermal environments more than 3,770 million years ago.
Evidence for early life in Earth’s oldest hydrothermal vent precipitates

USGS Publications Warehouse

Dodd, Matthew S.; Papineau, Dominic; Grenne, Tor; Slack, John F.; Rittner, Martin; Pirajno, Franco; O’Neil, Jonathan; Little, Crispin T.S.

2017-01-01

Although it is not known when or where life on Earth began, some of the earliest habitable environments may have been submarine-hydrothermal vents. Here we describe putative fossilized microorganisms that are at least 3,770 million and possibly 4,280 million years old in ferruginous sedimentary rocks, interpreted as seafloor-hydrothermal vent-related precipitates, from the Nuvvuagittuq belt in Quebec, Canada. These structures occur as micrometre-scale haematite tubes and filaments with morphologies and mineral assemblages similar to those of filamentous microorganisms from modern hydrothermal vent precipitates and analogous microfossils in younger rocks. The Nuvvuagittuq rocks contain isotopically light carbon in carbonate and carbonaceous material, which occurs as graphitic inclusions in diagenetic carbonate rosettes, apatite blades intergrown among carbonate rosettes and magnetite–haematite granules, and is associated with carbonate in direct contact with the putative microfossils. Collectively, these observations are consistent with an oxidized biomass and provide evidence for biological activity in submarine-hydrothermal environments more than 3,770 million years ago.
Results of hydraulic tests in U.S. Department of Energy's wells DOE-4, 5, 6, 7, 8, and 9, Salt Valley, Grand County, Utah

USGS Publications Warehouse

Wollitz, Leonard E.; Thordarson, William; Whitfield, Merrick S.; Weir, James E.

1982-01-01

Six exploratory wells were drilled into the cap rock underlying Salt Valley, Utah, for geologic, geophysical, and hydrologic data to augment information obtained from three previous test wells. Drilling of three other test holes was abandoned due to caving and loss of drilling tools, Before reaching the zone of saturation; the upper 100 meters of cap rock is unsaturated. Within the saturated part of the cap rock, hydraulic heads generally decrease with depth and to the northwest in this part of the valley.Hydraulic conductivity of the cap rock, as determined from pumping tests, ranged from 9.3 X 10-5 to 2.06 X 10-1 meters per day; as a result, groundwater flow rates in the cap rock are low. Water ranges from a calcium bicarbonate sulfate type on the western edge of the valley to a calcium magnesium sodium bicarbonate, sulfate, chloride type near the center of the valley. Carbon-14 specific activity for cap-rock water yielded an uncorrected age of about 17,000 to 26,000 years before present near the western edge of the valley and about 41,000 years before present near the center of the valley.
Radiocarbon as a Reactive Tracer for Tracking Permanent CO 2 Storage in Basaltic Rocks

DOE Office of Scientific and Technical Information (OSTI.GOV)

Matter, Juerg; Stute, Martin; Schlosser, Peter

In view of concerns about the long-term integrity and containment of CO 2 storage in geologic reservoirs, many efforts have been made to improve the monitoring, verification and accounting methods for geologically stored CO 2. Our project aimed to demonstrate that carbon-14 ( 14C) could be used as a reactive tracer to monitor geochemical reactions and evaluate the extent of mineral trapping of CO 2 in basaltic rocks. The capacity of a storage reservoir for mineral trapping of CO 2 is largely a function of host rock composition. Mineral carbonation involves combining CO 2 with divalent cations including Ca 2+,more » Mg 2+ and Fe 2+. The most abundant geological sources for these cations are basaltic rocks. Based on initial storage capacity estimates, we know that basalts have the necessary capacity to store million to billion tons of CO 2 via in situ mineral carbonation. However, little is known about CO2-fluid-rock reactions occurring in a basaltic storage reservoir during and post-CO 2 injection. None of the common monitoring and verification techniques have been able to provide a surveying tool for mineral trapping. The most direct method for quantitative monitoring and accounting involves the tagging of the injected CO 2 with 14C because 14C is not present in deep geologic reservoirs prior to injection. Accordingly, we conducted two CO 2 injection tests at the CarbFix pilot injection site in Iceland to study the feasibility of 14C as a reactive tracer for monitoring CO 2-fluid-rock reactions and CO 2 mineralization. Our newly developed monitoring techniques, using 14C as a reactive tracer, have been successfully demonstrated. For the first time, permanent and safe disposal of CO 2 as environmentally benign carbonate minerals in basaltic rocks could be shown. Over 95% of the injected CO 2 at the CarbFix pilot injection site was mineralized to carbonate minerals in less than two years after injection. Our monitoring results confirm that CO 2 mineralization in basaltic rocks is far faster than previously postulated.« less
Water-Rock Interactions in the Peridotite Aquifer of the Oman-UAE Ophiolite: Strontium Isotopic Ratio and Geochemical Evolution of Groundwater

NASA Astrophysics Data System (ADS)

Bompard, Nicolas; Matter, Juerg; Teagle, Damon

2016-04-01

The peridotite aquifer in Wadi Tayin, Sultanate of Oman, is a perfect example of natural carbonation of ultramafic rocks. In situ mineral carbonation is considered the most safest and permanent option of CO2 Capture and Sequestration (CCS). However, the process itself is yet to be characterised and a better understanding of the mechanisms involved in natural mineral carbonation is needed before geo-engineering it. We used the 87Sr/86Sr system to follow the water-rock interactions along the groundwater flowpath in the peridotite aquifer and to determine the sources of divalent cations (Mg2+, Ca2+) required for mineral carbonation. The Sr-isotope data of groundwater show that the aquifer rocks are the main source for divalent cations (Mg2+, Ca2+ and Sr2+) and secondary carbonates are their main sink. The groundwater 87Sr/86Sr ratio evolves with its pH: from 87Sr/86Sr = 0.7087 (n=3) to 0.7082 (n=8) between pH 7 and 8, and from 0.7086 (n=6) at pH 9 to 0.07075 (n=9) at pH 11. This evolution seems to support a two-step model for the water-rock interactions in the peridotite aquifer. From pH 7 to 8, secondary Ca-carbonate precipitation buffers the pH rise resulting from peridotite serpentinisation. From pH 9 to 11, peridotite serpentinisation drives the pH to alkaline condition. The change from a Mg-rich to a Ca-rich groundwater at pH 9 seems to confirm the two-step model.
Chemical Remagnetization of Jurassic Carbonates and a Primary Paleolatitude of Lower Cretaceous Volcaniclastic Rocks of the Tibetan Himalaya

NASA Astrophysics Data System (ADS)

Huang, W.; Van Hinsbergen, D. J. J.; Dekkers, M. J.; Garzanti, E.; Dupont Nivet, G.; Lippert, P. C.; Li, X.; Maffione, M.; Langereis, C. G.; Hu, X.; Guo, Z.; Kapp, P. A.

2014-12-01

Paleolatitudes for the Tibetan Himalaya Zone based on paleomagnetic inclinations provide kinematic constraints of the passive northern Indian margin and the extent of 'Greater India' before the India-Asia collision. Here, we present a paleomagnetic investigation of the Jurassic (carbonates) to Lower Cretaceous (volcaniclastic rocks) Wölong section of the Tibetan Himalaya in the Everest region. The carbonates yield positive fold tests, suggesting that the remanent magnetizations have a pre-folding origin. However, detailed paleomagnetic analyses, rock magnetic tests, end-member modeling of acquisition curves of isothermal remanent magnetization, and petrographic studies reveal that the magnetic carrier of the Jurassic carbonates is authigenic magnetite, whereas the dominant magnetic carrier of the Lower Cretaceous volcaniclastic rocks is detrital magnetite. We conclude that the Jurassic carbonates were remagnetized, whereas the Lower Cretaceous volcaniclastics retain a primary remanence. We hypothesize that remagnetization of the Jurassic carbonates was probably caused by the oxidation of early diagenetic pyrite to magnetite within the time interval at ~86-84 Ma during the latest Cretaceous Normal Superchron and earliest deposition of Cretaceous oceanic red beds in the Tibetan Himalaya. The remagnetization of the limestones prevents determining the size of 'Greater India' during Jurassic time. Instead, a paleolatitude of the Tibetan Himalaya of 23.8±2.1° S at ~86-84 Ma is suggested. This value is lower than the expected paleolatitude of India from apparent polar wander path (APWP). The volcaniclastic rocks with the primary remanence, however, yielded a Lower Cretaceous paleolatitude of Tibetan Himalaya of 55.5±3° S, fitting well with the APWP of India.
Minor-element composition and organic carbon content of marine and nonmarine shales of Late Cretaceous age in the western interior of the United States

USGS Publications Warehouse

Tourtelot, H.A.

1964-01-01

The composition of nonmarine shales of Cretaceous age that contain less than 1 per cent organic carbon is assumed to represent the inherited minor-element composition of clayey sediments delivered to the Cretaceous sea that occupied the western interior region of North America. Differences in minor-element content between these samples and samples of 1. (a) nonmarine carbonaceous shales (1 to 17 per cent organic carbon), 2. (b) nearshore marine shales (less than 1 per cent organic carbon), and 3. (c) offshore marine shales (as much as 8 per cent organic carbon), all of the same age, reveal certain aspects of the role played by clay minerals and organic materials in affecting the minor-element composition of the rocks. The organic carbon in the nonmarine rocks occurs in disseminated coaly plant remains. The organic carbon in the marine rocks occurs predominantly in humic material derived from terrestrial plants. The close similarity in composition between the organic isolates from the marine samples and low-rank coal suggests that the amount of marine organic material in these rocks is small. The minor-element content of the two kinds of nonmarine shales is the same despite the relatively large amount of organic carbon in the carbonaceous shales. The nearshore marine shales, however, contain larger median amounts of arsenic, boron, chromium, vanadium and zinc than do the nonmarine rocks; and the offshore marine shales contain even larger amounts of these elements. Cobalt, molybdenum, lead and zirconium show insignificant differences in median content between the nonmarine and marine rocks, although as much as 25 ppm molybdenum is present in some offshore marine samples. The gallium content is lower in the marine than in the nonmarine samples. Copper and selenium contents of the two kinds of nonmarine rocks and the nearshore marine samples are the same, but those of the offshore samples are larger. In general, arsenic, chromium, copper, molybdenum, selenium, vanadium and zinc are concentrated in those offshore marine samples having the largest amounts of organic carbon, but samples with equal amounts of vanadium, for instance, may differ by a factor of 3 in their amount of organic carbon. Arsenic and molybdenum occur in some samples chiefly in syngenetic pyrite but also are present in relatively large amounts in samples that contain little pyrite. The data on nonmarine carbonaceous shales indicate that organic matter of terrestrial origin in marine shales contributes little to the minor-element content of such rocks. It is possible that marine organic matter, even though seemingly small in amount in marine shales, contributes to the minor-element composition of the shales. In addition to any such contribution, however, the great effectiveness in sorption processes of humic materials in conjunction with clay minerals suggests that such processes must have played an important role as these materials moved from the relatively dilute solutions of the nonmarine environment to the relatively concentrated solution of sea water. The volumes of sea water sufficient to supply for sorption the amounts of most minor elements in the offshore marine samples are insignificant compared to the volumes of water with which the clay and organic matter were in contact during their transportation and sedimentation. Consequently, the chemical characteristics of the environment in which the clay minerals and organic matter accumulated and underwent diagenesis probably were the most important factors in controlling the degree to which sorption processes and the formation of syngenetic minerals affected the final composition of the rocks. ?? 1969.
Oxygen-Carbon and Strontium Isotope Evidence for the Origin and Evolution of CO2-rich Volatiles from Oligocene to Miocene Mantle Magmas, Southwestern Colorado and Northwestern New Mexico

NASA Astrophysics Data System (ADS)

Gonzales, D. A.; Zbrozek, M.

2012-12-01

Oligocene to Miocene, alkaline mafic to ultramafic, rocks that are exposed in the Navajo volcanic field and dikes on the northern San Juan basin (NVSJ) contain calcite in vugs, veins, and breccias. Oxygen-carbon and Sr isotope signatures of bulk carbonate samples from these rocks were used to test hypotheses on the history of volatiles related to this pulse of mantle magmatism. Elevated fluorine in rocks, and fluorite-calcite breccias in some outcrops, indicate that magmatic volatiles were released by NVSJ melts. Oxygen and carbon isotope data for carbonate samples record a complex paragenetic history. δ13C values are mostly -8‰ to -4‰ with a mean value of -5.3 ± 2.0‰, similar to δ13C for primary mantle-derived carbonate. A subset of δ18O values are +5‰ to +10‰ which are within the accepted range of δ18O values for magmatic carbonate in carbonatite and kimberlite. A majority of δ18O values, however, range from +10‰ to +24‰ revealing that low-δ18O magmatic volatiles were overprinted by processes that caused enrichment of 18O at some stage during melt generation and emplacement. A subset of 87Sr/86Sri data from carbonate samples are nearly identical to 87Sr/86Sri for related rocks, hinting that the melts and volatiles came from the same source. Generally, NVSJ calcite samples have higher 87Sr/86Sri ratios than those of rocks, reflecting different melt-volatile sources or crustal contamination from Paleozoic limestone. Field and petrologic evidence does not lend convincing support for crustal contamination. Limestone fragments comprise less than 1% of xenoliths in NVSJ rocks. Also, rock samples do not show elevated CaO, MgO, FeO, Ba or Sr with increasing δ18O calcite which is expected for contamination of magmas with limestone. We propose that CO2-H2O-F volatiles in NVSJ magmas came from distinct melt-volatile sources, similar to the interpretation of Nowell (1993). Our assertion is that CO2-rich volatiles that exsolved from low δ18O mafic melts interacted with volatiles and melts from carbonate-bearing metasomatized lithospheric mantle. This is consistent with the subtle increase of 87Sr/86Sri rock and fluorine over the +6‰ to +24‰ range of δ18Ocalcite values recorded in minette samples. This hypothesis is supported by other studies that document +21‰ to +25‰ δ18O for carbonate in mantle xenoliths from Pliocene alkaline basalts in the region. Incipient to extensive alteration of olivine and phlogopite phenocrysts in NVSJ rocks reveals that deuteric isotopic exchange with H2O-CO2 magmatic fluids was a plausible factor for some of the variation in δ18O of calcite samples. In addition, melt contamination with limestone cannot be ruled out, but it requires nearly complete digestion of xenoliths in feeder dikes that had relatively low volumes of magma and cooled quickly. Overall, the isotope data combined with field and petrologic results are not consistent with models that invoke groundwater as the main source of volatiles in NVSJ magmas.
Paleofacies of Eocene Lower Ngimbang Source Rocks in Cepu Area, East Java Basin based on Biomarkers and Carbon-13 Isotopes

NASA Astrophysics Data System (ADS)

Devi, Elok A.; Rachman, Faisal; Satyana, Awang H.; Fahrudin; Setyawan, Reddy

2018-02-01

The Eocene Lower Ngimbang carbonaceous shales are geochemically proven hydrocarbon source rocks in the East Java Basin. Sedimentary facies of source rock is important for the source evaluation that can be examined by using biomarkers and carbon-13 isotopes data. Furthermore, paleogeography of the source sedimentation can be reconstructed. The case study was conducted on rock samples of Lower Ngimbang from two exploration wells drilled in Cepu area, East Java Basin, Kujung-1 and Ngimbang-1 wells. The biomarker data include GC and GC-MS data of normal alkanes, isoprenoids, triterpanes, and steranes. Carbon-13 isotope data include saturate and aromatic fractions. Various crossplots of biomarker and carbon-13 isotope data of the Lower Ngimbang source samples from the two wells show that the source facies of Lower Ngimbang shales changed from transitional/deltaic setting at Kujung-1 well location to marginal marine setting at Ngimbang-1 well location. This reveals that the Eocene paleogeography of the Cepu area was composed of land area in the north and marine setting to the south. Biomarkers and carbon-13 isotopes are powerful data for reconstructing paleogeography and paleofacies. In the absence of fossils in some sedimentary facies, these geochemical data are good alternatives.
Carbonate Minerals with Magnesium in Triassic Terebratula Limestone in the Term of Limestone with Magnesium Application as a Sorbent in Desulfurization of Flue Gases

NASA Astrophysics Data System (ADS)

Stanienda-Pilecki, Katarzyna

2017-09-01

This article presents the results of studies of Triassic (Muschelkalk) carbonate rock samples of the Terebratula Beds taken from the area of the Polish part of the Germanic Basin. It is the area of Opole Silesia. The rocks were studied in the term of possibility of limestone with magnesium application in desulfurization of flue gases executed in power plants. Characteristic features of especially carbonate phases including magnesium-low-Mg calcite, high-Mg calcite, dolomite and huntite were presented in the article. They were studied to show that the presence of carbonate phases with magnesium, especially high-Mg calcite makes the desulfurization process more effective. Selected rock samples were examined using a microscope with polarized, transmitted light, X-ray diffraction, microprobe measurements and FTIR spectroscopy. The results of studies show a domination of low magnesium calcite in the limestones of the Terebratula Beds. In some samples dolomite and lower amounts of high-Mg calcite occurred. Moreover, huntite was identified. The studies were very important, because carbonate phases like high-Mg calcite and huntite which occurred in rocks of the Triassic Terebratula Beds were not investigated in details by other scientists but they presence in limestone sorbent could influence the effectiveness of desulfurization process.
Differences in dissolved organic matter lability between alpine glaciers and alpine rock glaciers of the American West

NASA Astrophysics Data System (ADS)

Hall, E.; Fegel, T. S., II; Baron, J.; Boot, C. M.

2015-12-01

While alpine glaciers in montane regions represent the largest flux of dissolved organic matter (DOM) from global ice melt no research has examined the bioavailability of DOM melted out of glacial ice in the western continental United States. Furthermore, rock glaciers are an order of magnitude more abundant than ice glaciers in U.S., yet are not included in budgets for perennial ice carbon stores. Our research aims to understand differences in the bioavailability of carbon from ice glaciers and rock glaciers along the Central Rocky Mountains of Colorado. Identical microbial communities were fed standardized amounts of DOM from four different ice glacier-rock glaciers pairs. Using laboratory incubations, paired with mass spectrometry based metabolomics and 16S gene sequencing; we were able to examine functional definitions of DOM lability in glacial ice. We hypothesized that even though DOM quantities are similar in the outputs of both glacial types in our study area, ice glacial DOM would be more bioavailable than DOM from rock glaciers due to higher proportions of byproducts from microbial metabolism than rock glacier DOM, which has higher amounts of "recalcitrant" plant material. Our results show that DOM from ice glaciers is more labile than DOM from geologically and geographically similar paired rock glaciers. Ice glacier DOM represents an important pool of labile carbon to headwater ecosystems of the Rocky Mountains. Metabolomic analysis shows numerous compounds from varying metabolite pathways, including byproducts of nitrification before and after incubation, meaning that, similar to large maritime glaciers in Alaska and Europe, subglacial environments in the mountain ranges of the United States are hotspots for biological activity and processing of organic carbon.
The geomechanical strength of carbonate rock in Kinta valley, Ipoh, Perak Malaysia

NASA Astrophysics Data System (ADS)

Mazlan, Nur Amanina; Lai, Goh Thian; Razib, Ainul Mardhiyah Mohd; Rafek, Abdul Ghani; Serasa, Ailie Sofyiana; Simon, Norbert; Surip, Noraini; Ern, Lee Khai; Mohamed, Tuan Rusli

2018-04-01

The stability of both cut rocks and underground openings were influenced by the geomechanical strength of rock materials, while the strength characteristics are influenced by both material characteristics and the condition of weathering. This paper present a systematic approach to quantify the rock material strength characteristics for material failure and material & discontinuities failure by using uniaxial compressive strength, point load strength index and Brazilian tensile strength for carbonate rocks. Statistical analysis of the results at 95 percent confidence level showed that the mean value of compressive strength, point load strength index and Brazilian tensile strength for with material failure and material & discontinuities failure were 76.8 ± 4.5 and 41.2 ± 4.1 MPa with standard deviation of 15.2 and 6.5 MPa, respectively. The point load strength index for material failure and material & discontinuities failure were 3.1 ± 0.2 MPa and 1.8 ± 0.3 MPa with standard deviation of 0.9 and 0.6 MPa, respectively. The Brazilian tensile strength with material failure and material & discontinuities failure were 7.1 ± 0.3 MPa and 4.1 ± 0.3 MPa with standard deviation of 1.4 and 0.6 MPa, respectively. The results of this research revealed that the geomechanical strengths of rock material of carbonate rocks for material & discontinuities failure deteriorates approximately ½ from material failure.
Finding of No Significant Impact: Military Family Housing Revitalization Project Nellis Air Force Base, Nevada

DTIC Science & Technology

2005-02-01

extent, plutonic rocks (all from the early Cenozoic Era). The sedimentary rocks are predominantly carbonates (limestone and dolomite), although there are...comprised of volcanic rocks, while the plutonic rocks also are exposed at a number of locations in the southern mountains (Longwell, et al., 1965

Response of Heterogeneous and Fractured Carbonate Samples to CO2-Brine Exposure

NASA Astrophysics Data System (ADS)

Smith, M. M.; Mason, H. E.; Hao, Y.; Carroll, S.

2014-12-01

Carbonate rock units are often considered as candidate sites for storage of carbon dioxide (CO2), whether as stand-alone reservoirs or coupled with enhanced oil recovery efforts. In order to accept injected carbon dioxide, carbonate reservoirs must either possess sufficient preexisting connected void space, or react with CO2-acidified fluids to produce more pore space and improve permeability. However, upward migration of CO2 through barrier zones or seal layers must be minimized for effective safe storage. Therefore, prediction of the changes to porosity and permeability in these systems over time is a key component of reservoir management. Towards this goal, we present the results of several experiments on carbonate core samples from the Wellington, Kansas 1-32 well, conducted under reservoir temperature, pressure, and CO2 conditions. These samples were imaged by X-ray computed tomography (XRCT) and analyzed with nuclear magnetic resonance (NMR) spectroscopy both prior to and after reaction with CO2-enriched brines. The carbonate samples each displayed distinct responses to CO2 exposure in terms of permeability change with time and relative abundance of calcite versus dolomite dissolution. The measured permeability of each sample was also much lower than that estimated by downhole NMR logging, with samples with larger fractured regions possessing higher permeability values. We present also our modeling approach and preliminary simulation results for a specific sample from the targeted injection zone. The heterogeneous composition as well as the presence of large fractured zones within the rock necessitated the use of a nested three-region approach to represent the range of void space observed via tomography. Currently, the physical response to CO2-brine flow (i.e., pressure declines with time) is reproduced well but the extent of chemical reaction is overestimated by the model.
Publications - GMC 416 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 416 Publication Details Title: Total organic carbon and rock-eval pyrolysis of core and core Resolution Inc. Analytical Laboratories, 2013, Total organic carbon and rock-eval pyrolysis of core and core Table(s) gmc416.xls (44.0 K) Keywords Organic Chemistry Top of Page Department of Natural Resources
Diffusive transport and reaction in clay rocks: A storage (nuclear waste, CO2, H2), energy (shale gas) and water quality issue

NASA Astrophysics Data System (ADS)

Charlet, Laurent; Alt-Epping, Peter; Wersin, Paul; Gilbert, Benjamin

2017-08-01

Clay rocks are low permeability sedimentary formations that provide records of Earth history, influence the quality of water resources, and that are increasingly used for the extraction or storage of energy resources and the sequestration of waste materials. Informed use of clay rock formations to achieve low-carbon or carbon-free energy goals requires the ability to predict the rates of diffusive transport processes for chemically diverse dissolved and gaseous species over periods up to thousands of years. We survey the composition, properties and uses of clay rock and summarize fundamental science challenges in developing confident conceptual and quantitative gas and solute transport models.
Monitoring carbonate dissolution using spatially resolved under-sampled NMR propagators and MRI

NASA Astrophysics Data System (ADS)

Sederman, A. J.; Colbourne, A.; Mantle, M. D.; Gladden, L. F.; Oliveira, R.; Bijeljic, B.; Blunt, M. J.

2017-12-01

The dissolution of a porous rock matrix by an acidic flow causes a change in the pore structure and consequently the pattern of fluid flow and rock permeability. This process is relevant to many areas of practical relevance such as enhanced oil recovery, water contaminant migration and sequestration of supercritical CO2. The most important governing factors for the type of change in the pore space are related by the Péclet (Pe) and Damköhler (Da) dimensionless numbers; these compare the transport properties of the fluid in the porous medium with the reactive properties of the solid matrix and the incident fluid respectively. Variation in Pe and Da can cause very different evolution regimes of the pore space and flow can occur, ranging from a uniform dissolution through different "wormholing" regimes (shown on the left hand side of figure 1) to face dissolution. NMR has a unique capability of measuring both the flow and structural changes during such dissolution whilst the characteristics of flow in the highly heterogeneous matrix that is formed can be predicted by the CTRW modelling approach. Here, NMR measurements of displacement probability distributions, or propagators, have been used to monitor the evolution of fluid flow during a reactive dissolution rock core floods. Developments in the NMR method by undersampling the acquisition data enable spatially resolved measurements of the propagators to be done at sufficient displacement resolution and in a timescale that is short enough to capture the changes in structure and flow. The highly under-sampled (4%) data, which typically reduces the acquisition time from 2 hours to 6 minutes, has been shown to produce equivalent propagator results to the fully sampled experiment. Combining these propagator measurements with quantitative and fast imaging techniques a full time-resolved picture of the dissolution reaction is built up. Experiments have been done for both Ketton and Estaillades carbonate rock cores, which exhibit very different dissolution behaviours, and for which experiments and model comparisons will be shown.
Role of rock/fluid characteristics in carbon (CO2) storage and modeling

USGS Publications Warehouse

Verma, Mahendra K.

2005-01-01

The presentation ? Role of Rock/Fluid Characteristics in Carbon (CO2) Storage and Modeling ? was prepared for the meeting of the Environmental Protection Agency (EPA) in Houston, Tex., on April 6?7, 2005. It provides an overview of greenhouse gases, particularly CO2, and a summary of their effects on the Earth?s atmosphere. It presents methods of mitigating the effects of greenhouse gases, and the role of rock and fluid properties on CO2 storage mechanisms. It also lists factors that must be considered to adequately model CO2 storage.
High-resolution delineation of chlorinated volatile organic compounds in a dipping, fractured mudstone: Depth- and strata-dependent spatial variability from rock-core sampling

NASA Astrophysics Data System (ADS)

Goode, Daniel J.; Imbrigiotta, Thomas E.; Lacombe, Pierre J.

2014-12-01

Synthesis of rock-core sampling and chlorinated volatile organic compound (CVOC) analysis at five coreholes, with hydraulic and water-quality monitoring and a detailed hydrogeologic framework, was used to characterize the fine-scale distribution of CVOCs in dipping, fractured mudstones of the Lockatong Formation of Triassic age, of the Newark Basin in West Trenton, New Jersey. From these results, a refined conceptual model for more than 55 years of migration of CVOCs and depth- and strata-dependent rock-matrix contamination was developed. Industrial use of trichloroethene (TCE) at the former Naval Air Warfare Center (NAWC) from 1953 to 1995 resulted in dense non-aqueous phase liquid (DNAPL) TCE and dissolved TCE and related breakdown products, including other CVOCs, in underlying mudstones. Shallow highly weathered and fractured strata overlie unweathered, gently dipping, fractured strata that become progressively less fractured with depth. The unweathered lithology includes black highly fractured (fissile) carbon-rich strata, gray mildly fractured thinly layered (laminated) strata, and light-gray weakly fractured massive strata. CVOC concentrations in water samples pumped from the shallow weathered and highly fractured strata remain elevated near residual DNAPL TCE, but dilution by uncontaminated recharge, and other natural and engineered attenuation processes, have substantially reduced concentrations along flow paths removed from sources and residual DNAPL. CVOCs also were detected in most rock-core samples in source areas in shallow wells. In many locations, lower aqueous concentrations, compared to rock core concentrations, suggest that CVOCs are presently back-diffusing from the rock matrix. Below the weathered and highly fractured strata, and to depths of at least 50 meters (m), groundwater flow and contaminant transport is primarily in bedding-plane-oriented fractures in thin fissile high-carbon strata, and in fractured, laminated strata of the gently dipping mudstones. Despite more than 18 years of pump and treat (P&T) remediation, and natural attenuation processes, CVOC concentrations in aqueous samples pumped from these deeper strata remain elevated in isolated intervals. DNAPL was detected in one borehole during coring at a depth of 27 m. In contrast to core samples from the weathered zone, concentrations in core samples from deeper unweathered and unfractured strata are typically below detection. However, high CVOC concentrations were found in isolated samples from fissile black carbon-rich strata and fractured gray laminated strata. Aqueous-phase concentrations were correspondingly high in samples pumped from these strata via short-interval wells or packer-isolated zones in long boreholes. A refined conceptual site model considers that prior to P&T remediation groundwater flow was primarily subhorizontal in the higher-permeability near surface strata, and the bulk of contaminant mass was shallow. CVOCs diffused into these fractured and weathered mudstones. DNAPL and high concentrations of CVOCs migrated slowly down in deeper unweathered strata, primarily along isolated dipping bedding-plane fractures. After P&T began in 1995, using wells open to both shallow and deep strata, downward transport of dissolved CVOCs accelerated. Diffusion of TCE and other CVOCs from deeper fractures penetrated only a few centimeters into the unweathered rock matrix, likely due to sorption of CVOCs on rock organic carbon. Remediation in the deep, unweathered strata may benefit from the relatively limited migration of CVOCs into the rock matrix. Synthesis of rock core sampling from closely spaced boreholes with geophysical logging and hydraulic testing improves understanding of the controls on CVOC delineation and informs remediation design and monitoring.
High-resolution delineation of chlorinated volatile organic compounds in a dipping, fractured mudstone: depth- and strata-dependent spatial variability from rock-core sampling

USGS Publications Warehouse

Goode, Daniel J.; Imbrigiotta, Thomas E.; Lacombe, Pierre J.

2014-01-01

Synthesis of rock-core sampling and chlorinated volatile organic compound (CVOC) analysis at five coreholes, with hydraulic and water-quality monitoring and a detailed hydrogeologic framework, was used to characterize the fine-scale distribution of CVOCs in dipping, fractured mudstones of the Lockatong Formation of Triassic age, of the Newark Basin in West Trenton, New Jersey. From these results, a refined conceptual model for more than 55 years of migration of CVOCs and depth- and strata-dependent rock-matrix contamination was developed. Industrial use of trichloroethene (TCE) at the former Naval Air Warfare Center (NAWC) from 1953 to 1995 resulted in dense non-aqueous phase liquid (DNAPL) TCE and dissolved TCE and related breakdown products, including other CVOCs, in underlying mudstones. Shallow highly weathered and fractured strata overlie unweathered, gently dipping, fractured strata that become progressively less fractured with depth. The unweathered lithology includes black highly fractured (fissile) carbon-rich strata, gray mildly fractured thinly layered (laminated) strata, and light-gray weakly fractured massive strata. CVOC concentrations in water samples pumped from the shallow weathered and highly fractured strata remain elevated near residual DNAPL TCE, but dilution by uncontaminated recharge, and other natural and engineered attenuation processes, have substantially reduced concentrations along flow paths removed from sources and residual DNAPL. CVOCs also were detected in most rock-core samples in source areas in shallow wells. In many locations, lower aqueous concentrations, compared to rock core concentrations, suggest that CVOCs are presently back-diffusing from the rock matrix. Below the weathered and highly fractured strata, and to depths of at least 50 meters (m), groundwater flow and contaminant transport is primarily in bedding-plane-oriented fractures in thin fissile high-carbon strata, and in fractured, laminated strata of the gently dipping mudstones. Despite more than 18 years of pump and treat (P&T) remediation, and natural attenuation processes, CVOC concentrations in aqueous samples pumped from these deeper strata remain elevated in isolated intervals. DNAPL was detected in one borehole during coring at a depth of 27 m. In contrast to core samples from the weathered zone, concentrations in core samples from deeper unweathered and unfractured strata are typically below detection. However, high CVOC concentrations were found in isolated samples from fissile black carbon-rich strata and fractured gray laminated strata. Aqueous-phase concentrations were correspondingly high in samples pumped from these strata via short-interval wells or packer-isolated zones in long boreholes. A refined conceptual site model considers that prior to P&T remediation groundwater flow was primarily subhorizontal in the higher-permeability near surface strata, and the bulk of contaminant mass was shallow. CVOCs diffused into these fractured and weathered mudstones. DNAPL and high concentrations of CVOCs migrated slowly down in deeper unweathered strata, primarily along isolated dipping bedding-plane fractures. After P&T began in 1995, using wells open to both shallow and deep strata, downward transport of dissolved CVOCs accelerated. Diffusion of TCE and other CVOCs from deeper fractures penetrated only a few centimeters into the unweathered rock matrix, likely due to sorption of CVOCs on rock organic carbon. Remediation in the deep, unweathered strata may benefit from the relatively limited migration of CVOCs into the rock matrix. Synthesis of rock core sampling from closely spaced boreholes with geophysical logging and hydraulic testing improves understanding of the controls on CVOC delineation and informs remediation design and monitoring.
Compaction of basin sediments as a function of time-temperature history

DOE Office of Scientific and Technical Information (OSTI.GOV)

Schmoker, J.W.; Gautier, D.L.

1989-03-01

Processes that affect burial diagenesis are dependent on time-temperature history (thermal maturity). Therefore, the porosity loss of sedimentary rocks during burial may often be better treated as a function of time-temperature history than of depth. Loss of porosity in the subsurface for sandstones, carbonates, and shales can be represented by a power function /phi/ = A(M)/sup B/, where /phi/ is porosity, A and B are constants for a given sedimentary rock population of homogeneous properties, and M is a measure of thermal maturity such as vitrinite reflectance (R/sub 0/) or Lopatin's time-temperature index (TTI). Regression lines of carbonate porosity andmore » of sandstone porosity upon thermal maturity form an envelope whose axis is approximated by /phi/ = 7.5(R/sub 0/)/sup /minus/1.18/ or, equivalently, by /phi/ = 30(TTI)/sup /minus/0.33/. These equations are preliminary generic relations of use for the regional modeling of both carbonate and sandstone compaction in sedimentary basins. The dependence of porosity upon time-temperature history incorporates the hypothesis that porosity-reducing processes operate continuously in sedimentary basins and, consequently, that compaction of basin sediments continues as long as porosity exists. Calculations indicate that subsidence due to loss of porosity through time (with depth held constant) can produce a second-stage passively formed basin in which many hundreds of meters of sediments can accumulate and which conforms with the structure of the original underlying basin. Such sediment accumulation results from the thermal maturation of thick sequences of sedimentary rocks rather than from global sea level change or tectonic subsidence.« less
[Effect of hydrochemistry characteristics under impact of human activity: a case study in the upper reaches of the Xijiang River basin].

PubMed

Yu, Shil; Sun, Ping-an; Du, Wen-yue; He, Shi-yi; Li, Rui

2015-01-01

In this paper, observation and sampling were taken three times a month in a hydrological year for three typical sections of the middle and upper reaches of the Xijiang River basin, based on the data of hydrochemistry and flow, the article mainly discusses the evolution process of hydrochemistry in river under natural process and impact of human activity. Hydrochemical characteristics of 116. samples were analyzed in the study area. The hydrochemistry type in the middle and upper reaches of the Xijiang River basin belonged to HCO3- -Ca2+ type, and the chemical weathering type mainly came from carbonate rock weathering. Ca2+ and HCO3- were the main cations and anions, which reflected that hydrochemical characteristics of river in karst area mainly affected by the dissolution of carbonate rock. Na, Mg2, Ca2+ and Cl- mainly affected by natural conditions, the impact of human activity was little. K+, NO3-, SO4(2-) and HCO3- were affected by human activity in different degrees, and it showed different influence ways. This study had an important significance for the change of river hydrochemistry, water quality characteristics, and the effect on substance transported fluxes in the downstream of Pearl River and water quality protection in South China Monsoon Area.
Major influencing factors of indoor radon concentrations in Switzerland.

PubMed

Kropat, Georg; Bochud, Francois; Jaboyedoff, Michel; Laedermann, Jean-Pascal; Murith, Christophe; Palacios, Martha; Baechler, Sébastien

2014-03-01

In Switzerland, nationwide large-scale radon surveys have been conducted since the early 1980s to establish the distribution of indoor radon concentrations (IRC). The aim of this work was to study the factors influencing IRC in Switzerland using univariate analyses that take into account biases caused by spatial irregularities of sampling. About 212,000 IRC measurements carried out in more than 136,000 dwellings were available for this study. A probability map to assess risk of exceeding an IRC of 300 Bq/m(3) was produced using basic geostatistical techniques. Univariate analyses of IRC for different variables, namely the type of radon detector, various building characteristics such as foundation type, year of construction and building type, as well as the altitude, the average outdoor temperature during measurement and the lithology, were performed comparing 95% confidence intervals among classes of each variable. Furthermore, a map showing the spatial aggregation of the number of measurements was generated for each class of variable in order to assess biases due to spatially irregular sampling. IRC measurements carried out with electret detectors were 35% higher than measurements performed with track detectors. Regarding building characteristics, the IRC of apartments are significantly lower than individual houses. Furthermore, buildings with concrete foundations have the lowest IRC. A significant decrease in IRC was found in buildings constructed after 1900 and again after 1970. Moreover, IRC decreases at higher outdoor temperatures. There is also a tendency to have higher IRC with altitude. Regarding lithology, carbonate rock in the Jura Mountains produces significantly higher IRC, almost by a factor of 2, than carbonate rock in the Alps. Sedimentary rock and sediment produce the lowest IRC while carbonate rock from the Jura Mountains and igneous rock produce the highest IRC. Potential biases due to spatially unbalanced sampling of measurements were identified for several influencing factors. Significant associations were found between IRC and all variables under study. However, we showed that the spatial distribution of samples strongly affected the relevance of those associations. Therefore, future methods to estimate local radon hazards should take the multidimensionality of the process of IRC into account. Copyright © 2013 Elsevier Ltd. All rights reserved.
Pore-scale Simulation and Imaging of Multi-phase Flow and Transport in Porous Media (Invited)

NASA Astrophysics Data System (ADS)

Crawshaw, J.; Welch, N.; Daher, I.; Yang, J.; Shah, S.; Grey, F.; Boek, E.

2013-12-01

We combine multi-scale imaging and computer simulation of multi-phase flow and reactive transport in rock samples to enhance our fundamental understanding of long term CO2 storage in rock formations. The imaging techniques include Confocal Laser Scanning Microscopy (CLSM), micro-CT and medical CT scanning, with spatial resolutions ranging from sub-micron to mm respectively. First, we report a new sample preparation technique to study micro-porosity in carbonates using CLSM in 3 dimensions. Second, we use micro-CT scanning to generate high resolution 3D pore space images of carbonate and cap rock samples. In addition, we employ micro-CT to image the processes of evaporation in fractures and cap rock degradation due to exposure to CO2 flow. Third, we use medical CT scanning to image spontaneous imbibition in carbonate rock samples. Our imaging studies are complemented by computer simulations of multi-phase flow and transport, using the 3D pore space images obtained from the scanning experiments. We have developed a massively parallel lattice-Boltzmann (LB) code to calculate the single phase flow field in these pore space images. The resulting flow fields are then used to calculate hydrodynamic dispersion using a novel scheme to predict probability distributions for molecular displacements using the LB method and a streamline algorithm, modified for optimal solid boundary conditions. We calculate solute transport on pore-space images of rock cores with increasing degree of heterogeneity: a bead pack, Bentheimer sandstone and Portland carbonate. We observe that for homogeneous rock samples, such as bead packs, the displacement distribution remains Gaussian with time increasing. In the more heterogeneous rocks, on the other hand, the displacement distribution develops a stagnant part. We observe that the fraction of trapped solute increases from the beadpack (0 %) to Bentheimer sandstone (1.5 %) to Portland carbonate (8.1 %), in excellent agreement with PFG-NMR experiments. We then use our preferred multi-phase model to directly calculate flow in pore space images of two different sandstones and observe excellent agreement with experimental relative permeabilities. Also we calculate cluster size distributions in good agreement with experimental studies. Our analysis shows that the simulations are able to predict both multi-phase flow and transport properties directly on large 3D pore space images of real rocks. Pore space images, left and velocity distributions, right (Yang and Boek, 2013)
Experiment and simulation study on the effects of cement minerals on the water-rock-CO2 interaction during CO2 geological storage

NASA Astrophysics Data System (ADS)

Liu, N.; Cheng, J.

2016-12-01

The CO2 geological storage is one of the most promising technology to mitigate CO2 emission. The fate of CO2 underground is dramatically affected by the CO2-water-rock interaction, which are mainly dependent on the initial aquifer mineralogy and brine components. The cement minerals are common materials in sandstone reservoir but few attention has been paid for its effects on CO2-water-rock interaction. Five batch reactions, in which 5% cement minerals were assigned to be quartz, calcite, dolomite, chlorite and Ca-montmorillonite, respectively, were conducted to understanding the cement minerals behaviors and its corresponding effects on the matrix minerals alterations during CO2 geological storage. Pure mineral powders were selected to mix and assemble the 'sandstone rock' with different cement components meanwhile keeping the matrix minerals same for each group as 70% quartz, 20% K-feldspar and 5% albite. These `rock' reacted with 750ml deionized water and CO2 under 180° and 18MPa for 15 days, during which the water chemistry evolution and minerals surface micromorphology changes has been monitored. The minerals saturation indexes calculation and phase diagram as well as the kinetic models were made by PHREEQC to uncover the minerals reaction paths. The experiment results indicated that the quartz got less eroded, on the contrary, K-feldspar and albite continuously dissolved to favor the gibbsite and kaolinite precipitations. The carbonates cement minerals quickly dissolved to reach equilibrium with the pH buffered and in turn suppressed the alkali feldspar dissolutions. No carbonates minerals precipitations occurred until the end of reactions for all groups. The simulation results were basically consistent with the experiment record but failed to simulate the non-stoichiometric reactions and the minerals kinetic rates seemed underestimated at the early stage of reactions. The cement minerals significantly dominated the reaction paths during CO2 geological storage and its effects on the CO2-water-rock interaction should be focused no matter for the benefit of injection sustainability or carbon sequestration capability. And more cement minerals such as ankerite should be included and the reservoir quality changes should also be taken consideration in the further study.
Carbonation of Subduction Interface Ultramafic Rocks and Implications for Deep Carbon Cycling: Evidence from Hybrid Serpentinite-Marble in the Voltri Massif, Italy

NASA Astrophysics Data System (ADS)

Scambelluri, M.; Bebout, G. E.; Gilio, M.; Belmonte, D.; Campomenosi, N.; Crispini, L.

2015-12-01

Release of COH fluids from hydrous minerals and carbonates influences element recycling and magmatism at subduction zones. Contradictory interpretations exist regarding the retention/storage of C in subducting plates and in the forearc to subarc mantle. Multiple lines of evidence indicate mobility of C in forearcs; however, the magnitude of this loss is highly uncertain[1-5]. A poorly constrained fraction of the 40-115 Mt/y of C initially subducted is released into fluids (e.g., by decarbonation, carbonate dissolution), and 18-43 Mt/y is returned at arc volcanoes[2-5, refs. therein]. The imbalance could reflect subduction into the deeper mantle or forearc/subarc storage[4-7]. We examine the fate of C in slab/interface ultramafic rocks, and by analogy serpentinized mantle wedge, via study of fluid-rock evolution of marble and variably carbonated serpentinite (Ligurian Alps). Based on petrography, and major/trace element and C and O isotope compositions, we demonstrate that serpentinite dehydration at 2-2.5 GPa, 550°C released aqueous fluids triggering breakdown of dolomite in nearby marbles, thus releasing C into fluids. Carbonate + olivine veins document flow of COH fluids; interaction of these COH fluids with serpentinite led to formation of high-pressure carbonated ultramafic-rock domains, thus resulting in retention of C in some rocks at an ancient subduction interface. We stress that lithologically complex interfaces could contain sites of both C release and C addition, further confounding estimates of net C loss at forearc and subarc depths [cf 4,5]. Sites of C retention, also including carbonate veins and graphite as reduced carbonate[7], could influence the transfer of slab C to at least the depths beneath volcanic fronts. 1. Poli S et al. 2009 EPSL; 2. Ague and Nicolescu 2014 Nat Geosci; 3. Cook-Collars et al. 2014 Chem Geol; 4. Collins et al. 2015 Chem Geol; 5. Kelemen and Manning 2015 PNAS; 6. Sapienza et al. 2009 CMP; 7 Galvez et al. 2013 Nat Geosci
Dynamic Pore-Scale Imaging of Reactive Transport in Heterogeneous Carbonates at Reservoir Conditions Across Multiple Dissolution Regimes

NASA Astrophysics Data System (ADS)

Menke, H. P.; Bijeljic, B.; Andrew, M. G.; Blunt, M. J.

2014-12-01

Sequestering carbon in deep geologic formations is one way of reducing anthropogenic CO2 emissions. When supercritical CO2 mixes with brine in a reservoir, the acid generated has the potential to dissolve the surrounding pore structure. However, the magnitude and type of dissolution are condition dependent. Understanding how small changes in the pore structure, chemistry, and flow properties affect dissolution is paramount for successful predictive modelling. Both 'Pink Beam' synchrotron radiation and a Micro-CT lab source are used in dynamic X-ray microtomography to investigate the pore structure changes during supercritical CO2 injection in carbonate rocks of varying heterogeneity at high temperatures and pressures and various flow-rates. Three carbonate rock types were studied, one with a homogeneous pore structure and two heterogeneous carbonates. All samples are practically pure calcium carbonate, but have widely varying rock structures. Flow-rate was varied in three successive experiments by over an order of magnitude whlie keeping all other experimental conditions constant. A 4-mm carbonate core was injected with CO2-saturated brine at 10 MPa and 50oC. Tomographic images were taken at 30-second to 20-minute time-resolutions during a 2 to 4-hour injection period. A pore network was extracted using a topological analysis of the pore space and pore-scale flow modelling was performed directly on the binarized images with connected pathways and used to track the altering velocity distributions. Significant differences in dissolution type and magnitude were found for each rock type and flowrate. At the highest flow-rates, the homogeneous carbonate was seen to have predominately uniform dissolution with minor dissolution rate differences between the pores and pore throats. Alternatively, the heterogeneous carbonates which formed wormholes at high flow rates. At low flow rates the homogeneous rock developed wormholes, while the heterogeneous samples showed evidence of compact dissolution. This study serves as a unique benchmark for pore-scale reactive transport modelling directly on the binarized Micro-CT images. Dynamic pore-scale imaging methods offer advantages in helping explain the dominant processes at the pore scale so that they may be up-scaled for accurate model prediction.
A molecular and isotopic study of the organic matter from the Paris Basin, France

NASA Technical Reports Server (NTRS)

Lichtfouse, E.; Albrecht, P.; Behar, F.; Hayes, J. M.

1994-01-01

Thirteen Liassic sedimentary rocks of increasing depth and three petroleums from the Paris Basin were studied for 13C/12C isotopic compositions and biological markers, including steranes, sterenes, methylphenanthrenes, methylanthracenes, and triaromatic steroids. The isotopic compositions of n-alkanes from mature sedimentary rocks and petroleums fall in a narrow range (2%), except for the deepest Hettangian rock and the Trias petroleum, for which the short-chain n-alkanes are enriched and depleted in 13C, respectively. Most of the molecular parameters increase over the 2000-2500 m depth range, reflecting the transformation of the organic matter at the onset of petroleum generation. In this zone, carbonate content and carbon isotopic composition of carbonates, as well as molecular parameters, are distinct for the Toarcian and Hettangian source rocks and suggest a migration of organic matter from these two formations. Two novel molecular parameters were defined for this task: one using methyltriaromatic steroids from organic extracts; the other using 1-methylphenanthrene and 2-methylanthracene from kerogen pyrolysates. The anomalous high maturity of the Dogger petroleum relative to the maturity-depth trend of the source rocks is used to estimate the minimal vertical distance of migration of the organic matter from the source rock to the reservoir.
Geological carbon budget of the Mackenzie River Basin: New insight from the oxidation of rock-derived organic carbon

NASA Astrophysics Data System (ADS)

Horan, K.; Hilton, R. G.; Dellinger, M.; Galy, V.; Gaillardet, J.; Tipper, E.; Selby, D. S.; Ottley, C. J.; Burton, K. W.

2016-12-01

Erosion and weathering transfer carbon between the atmosphere and lithospheric storage, thereby operating to modify Earth's long-term climate. Over millions of years, atmospheric carbon dioxide (CO2) is sequestered during the weathering of silicate minerals by carbonic acid, coupled to carbonate formation, and following the erosion of biospheric organic carbon and its burial in sediments. However, erosion and weathering also act together to release CO2 from the lithosphere. Erosion enhances the rate of oxidative weathering of organic carbon in rocks (petrogenic OC, OCpetro), which is a major CO2 source over geological time. In addition, oxidation of sulfide minerals can produce sulfuric acid that weathers carbonate minerals and results in transient CO2 release. Although these sources and sinks of CO2 are well recognised, limited case studies exist where they have been measured alongside each other. Here we calculate the geological carbon budget during weathering and erosion in the Mackenzie River Basin, Canada. The silicate weathering rate, carbonate weathering rate by sulfuric acid and the sedimentary burial of biospheric organic carbon have been constrained by prior work. Closing the long-term CO2 budget therefore requires us to quantify the OCpetro oxidation rate. To do this, we use dissolved rhenium (Re) concentrations as a proxy for OCpetro weathering using samples collected from 2009 to 2013. We normalise dissolved river Re concentrations to the rock Re concentration ([Re]diss/[Re]rock) to assess the variability in oxidative weathering efficiency. We find [Re]diss/[Re]rock ratios are 2-4 times lower than those calculated for rapidly eroding mountain catchments (e.g. Taiwan), which is consistent with a lower physical erosion rate in the Mackenzie Basin. By making assumptions about the concurrent mobility of Re and CO2 during OCpetro weathering we quantify the OCpetro weathering rate and constrain the associated CO2 flux to be 0.3 tC km-2 yr-1. The transient CO2 release by sulfuric acid driven carbonate weathering is 0.8 tC km-2 yr-1. Therefore, these two CO2 sources counter CO2 drawdown by silicate weathering (0.4 tC km-2 yr-1). Nevertheless, OCpetro oxidation does not negate the large CO2 sink driven by biospheric organic carbon erosion (2 tC km-2 yr-1), so the Mackenzie Basin is presently a CO2 sink.
Geologic assessment of undiscovered oil and gas resources—Lower Cretaceous Albian to Upper Cretaceous Cenomanian carbonate rocks of the Fredericksburg and Washita Groups, United States Gulf of Mexico Coastal Plain and State Waters

USGS Publications Warehouse

Swanson, Sharon M.; Enomoto, Catherine B.; Dennen, Kristin O.; Valentine, Brett J.; Cahan, Steven M.

2017-02-10

In 2010, the U.S. Geological Survey (USGS) assessed Lower Cretaceous Albian to Upper Cretaceous Cenomanian carbonate rocks of the Fredericksburg and Washita Groups and their equivalent units for technically recoverable, undiscovered hydrocarbon resources underlying onshore lands and State Waters of the Gulf Coast region of the United States. This assessment was based on a geologic model that incorporates the Upper Jurassic-Cretaceous-Tertiary Composite Total Petroleum System (TPS) of the Gulf of Mexico basin; the TPS was defined previously by the USGS assessment team in the assessment of undiscovered hydrocarbon resources in Tertiary strata of the Gulf Coast region in 2007. One conventional assessment unit (AU), which extends from south Texas to the Florida panhandle, was defined: the Fredericksburg-Buda Carbonate Platform-Reef Gas and Oil AU. The assessed stratigraphic interval includes the Edwards Limestone of the Fredericksburg Group and the Georgetown and Buda Limestones of the Washita Group. The following factors were evaluated to define the AU and estimate oil and gas resources: potential source rocks, hydrocarbon migration, reservoir porosity and permeability, traps and seals, structural features, paleoenvironments (back-reef lagoon, reef, and fore-reef environments), and the potential for water washing of hydrocarbons near outcrop areas.In Texas and Louisiana, the downdip boundary of the AU was defined as a line that extends 10 miles downdip of the Lower Cretaceous shelf margin to include potential reef-talus hydrocarbon reservoirs. In Mississippi, Alabama, and the panhandle area of Florida, where the Lower Cretaceous shelf margin extends offshore, the downdip boundary was defined by the offshore boundary of State Waters. Updip boundaries of the AU were drawn based on the updip extent of carbonate rocks within the assessed interval, the presence of basin-margin fault zones, and the presence of producing wells. Other factors evaluated were the middle Cenomanian sea-level fall and erosion that removed large portions of platform and platform-margin carbonate sediments in the Washita Group of central Louisiana. The production history of discovered reservoirs and well data within the AU were examined to estimate the number and size of undiscovered oil and gas reservoirs within the AU. Using the USGS National Oil and Gas Assessment resource assessment methodology, mean volumes of 40 million barrels of oil, 622 billion cubic feet of gas, and 14 million barrels of natural gas liquids are the estimated technically recoverable undiscovered resources for the Fredericksburg-Buda Carbonate Platform-Reef Gas and Oil AU.
Microstructural record of cataclastic and dissolution-precipitation processes from shallow crustal carbonate strike-slip faults, Northern Calcareous Alps (Austria)

NASA Astrophysics Data System (ADS)

Bauer, Helene; Grasemann, Bernhard; Decker, Kurt

2015-04-01

The concept of coseismic slip and aseismic creep deformation along faults is supported by the variability of natural fault rocks and their microstructures. Faults in carbonate rocks are characterized by very narrow principal slip zones (cm to mm wide) containing (ultra)cataclastic fault rocks that accommodate most of the fault displacement. Fluidization of ultracataclastic sub layers and thermal decomposition of calcite due to frictional heating have been proposed as possible indicators for seismic slip. Dissolution-precipitation (DP) processes are possible mechanism of aseismic sliding, resulting in spaced cleavage solution planes and associated veins, indicating diffusive mass transfer and precipitation in pervasive vein networks. We investigated exhumed, sinistral strike-slip faults in carbonates of the Northern Calcareous Alps. The study presents microstructural investigations of natural carbonate fault rocks that formed by cataclastic and dissolution-precipitation related deformation processes. Faults belong to the eastern segment of the Salzachtal-Ennstal-Mariazell-Puchberg (SEMP) fault system that was formed during eastward lateral extrusion of the Eastern Alps in Oligocene to Lower Miocene. The investigated faults accommodated sinistral slip between several tens and few hundreds of meters. Microstructural analysis of fault rocks was done with scanning electron microscopy and optical microscopy. Deformation experiments of natural fault rocks are planned to be conducted at the Sapienza University of Roma and should be available at the meeting. The investigated fault rocks give record of alternating cataclastic deformation and DP creep. DP fault rocks reveal various stages of evolution including early stylolites, pervasive pressure solution seams and cleavage, localized shear zones with syn-kinematic calcite fibre growth and mixed DP/cataclastic microstructures, involving pseudo sc- and scc'-fabrics. Pressure solution seams host fine grained kaolinit, chlorite and illite while the protolith shows only weak evidence of detrital clay content. Our studies suggest that velocity weakening and strengthening mechanisms alternated during the accumulation of displacement along the SEMP fault zone.
Uplift of continental crustal blocks adjacent to the Rancheria Basin-Guasare area: the effects of Maastrichtian-Paleocene collision along the southern Caribbean plate boundary

NASA Astrophysics Data System (ADS)

Bayona, G.; Montes, C.; Jaramillo, C.; Ojeda, G.; Cardona, A.; Pardo, A.; Lamus, F.

2007-05-01

In the Rancheria basin (RB) and Guasare area (GA), Maastrichtian-Paleocene synorogenic strata overlie the Aptian-Campanian carbonate platform. Nowadays, RB is bounded to the west by metamorphic-and-igneous cored Santa Marta massif, where Upper Cretaceous strata overlie unconformably pre-Cretaceous rocks. The eastern boundary of the RB is the Perija range that includes volcaniclastic and sedimentary rocks of Jurassic and Cretaceous age in the hanging-wall of a NW-verging, low-angle dipping thrust belt. The GA is on the eastern foothills of the Perija range and corresponds to the western boundary of the Maracaibo basin. Strata architecture, seismic reflectors, gravity, provenance, and paleocurrent analyses carried out in those basins constrain the timing and style of uplift of Santa Marta massif and Perija range, which are linked with tectonism along the southern Caribbean plate. Maastrichtian-Paleocene strata thicken eastward up to 2.2 km in the RB, and this succession includes (in stratigraphic order): foram-rich calcareous mudstone, oyster-pelecypod rich carbonate-siliciclastic strata, coal- bearing mudstones and feldspar-lithic-rich fluvial sandstones. Internal disconformities and truncations of seismic reflectors are identified to the west of the RB, but there are not major thrust faults at this part of the basin to explain such unconformities and truncations. In Early Paleocene, carbonates developed better to the west of the RB, whereas mixed carbonate-siliciclastic deposition continued toward the east of the RB. In early Late Paleocene, influx of terrigenous material (key grains=metamorphic, microcline and garnet fragments) derived from the Santa Marta massif increased to the west, but to the east of the RB and GA carbonate-siliciclastic and carbonate deposition continued, respectively. In mid-Late Paleocene, diachronous eastward advance of paralic/deltaic environments, tropical humid climate, and high subsidence rates favored production and preservation of peat in RB and GA. In the late Late Paleocene, inversion along a buried graben system under the Perija range explain supply toward RB and GA of micritic, volcanic, and sedimentary rock fragments, and the record of a thinner Upper Paleocene strata in the GA than in the RB. Tectonic subsidence in the RB was mainly related to pivoting of the Santa Marta massif as result of collision of the Maracaibo continental sub-plate with the southern margin of the Caribbean oceanic plate. This model explains the generation of accommodation space in the RB without faulting, denudation of upper crustal material of the Santa Marta massif, early capture of terrigenous detritus in the RB that favored carbonate deposition in the GA, the mechanism of initial inversion of the Perija range, and the present positive gravity anomaly under the Santa Marta massif.
Weathering profiles in soils and rocks on Earth and Mars

NASA Astrophysics Data System (ADS)

Hausrath, E.; Adcock, C. T.; Bamisile, T.; Baumeister, J. L.; Gainey, S.; Ralston, S. J.; Steiner, M.; Tu, V.

2017-12-01

Interactions of liquid water with rock, soil, or sediments can result in significant chemical and mineralogical changes with depth. These changes can include transformation from one phase to another as well as translocation, addition, and loss of material. The resulting chemical and mineralogical depth profiles can record characteristics of the interacting liquid water such as pH, temperature, duration, and abundance. We use a combined field, laboratory, and modeling approach to interpret the environmental conditions preserved in soils and rocks. We study depth profiles in terrestrial field environments; perform dissolution experiments of primary and secondary phases important in soil environments; and perform numerical modeling to quantitatively interpret weathering environments. In our field studies we have measured time-integrated basaltic mineral dissolution rates, and interpreted the impact of pH and temperature on weathering in basaltic and serpentine-containing rocks and soils. These results help us interpret fundamental processes occurring in soils on Earth and on Mars, and can also be used to inform numerical modeling and laboratory experiments. Our laboratory experiments provide fundamental kinetic data to interpret processes occurring in soils. We have measured dissolution rates of Mars-relevant phosphate minerals, clay minerals, and amorphous phases, as well as dissolution rates under specific Mars-relevant conditions such as in concentrated brines. Finally, reactive transport modeling allows a quantitative interpretation of the kinetic, thermodynamic, and transport processes occurring in soil environments. Such modeling allows the testing of conditions under longer time frames and under different conditions than might be possible under either terrestrial field or laboratory conditions. We have used modeling to examine the weathering of basalt, olivine, carbonate, phosphate, and clay minerals, and placed constraints on the duration, pH, and solution chemistry of past aqueous alteration occurring on Mars.

Carbonate ions and arsenic dissolution by groundwater

USGS Publications Warehouse

Kim, M.-J.; Nriagu, J.; Haack, S.

2000-01-01

Samples of Marshall Sandstone, a major source of groundwater with elevated arsenic levels in southeast Michigan, were exposed to bicarbonate ion under controlled chemical conditions. In particular, effects of pH and redox conditions on arsenic release were evaluated. The release of arsenic from the aquifer rock was strongly related to the bicarbonate concentration in the leaching solution. The results obtained suggest that the carbonation of arsenic sulfide minerals, including orpiment (As2S3) and realgar (As2S2), is an important process in leaching arsenic into groundwater under anaerobic conditions. The arseno-carbonate complexes formed, believed to be As(CO3)2-, As(CO3)(OH)2-, and AsCO3+, are stable in groundwater. The reaction of ferrous ion with the thioarsenite from carbonation process can result in the formation of arsenopyrite which is a common mineral in arsenic-rich aquifers.Samples of Marshall Sandstone, a major source of groundwater with elevated arsenic levels in southeast Michigan, were exposed to bicarbonate ion under controlled chemical conditions. In particular, effects of pH and redox conditions on arsenic release were evaluated. The release of arsenic from the aquifer rock was strongly related to the bicarbonate concentration in the leaching solution. The results obtained suggest that the carbonation of arsenic sulfide minerals, including orpiment (As2S3) and realgar (As2S2), is an important process in leaching arsenic into groundwater under anaerobic conditions. The arseno-carbonate complexes formed, believed to be As(CO3)2-, As(CO3)(OH)2-, and AsCO3+, are stable in groundwater. The reaction of ferrous ion with the thioarsenite from carbonation process can result in the formation of arsenopyrite which is a common mineral in arsenic-rich aquifers.The role of bicarbonate in leaching arsenic into groundwater was investigated by conducting batch experiments using core samples of Marshall Sandstone from southeast Michigan and different bicarbonate solutions. The effects of pH and redox conditions on As dissolution were examined. Results showed that As was not leached significantly out of the Marshall Sandstone samples after 3 d using either deionized water or groundwater, but As was leached efficiently by sodium bicarbonate, potassium bicarbonate, and ferric chloride solutions. The leaching rate with sodium bicarbonate was about 25% higher than that with potassium bicarbonate. The data indicated that bicarbonate ion was involved primarily in As dissolution and that hydroxyl radical ion did not affect As dissolution to any significant degree. The amount of As leached was dependent upon the sodium bicarbonate concentration, increasing with reaction time for each concentration. Significant As leaching was found in the extreme pH ranges of <1.9 and 8.0-10.4. The resulting arseno-carbonate complexes formed were stable in groundwater.
delta 15N and non-carbonate delta 13C values for two petroleum source rock reference materials and a marine sediment reference material

USGS Publications Warehouse

Dennen, Kristin O.; Johnson, Craig A.; Otter, Marshall L.; Silva, Steven R.; Wandless, Gregory A.

2006-01-01

Samples of United States Geological Survey (USGS) Certified Reference Materials USGS Devonian Ohio Shale (SDO-1), and USGS Eocene Green River Shale (SGR-1), and National Research Council Canada (NRCC) Certified Marine Sediment Reference Material (PACS-2), were sent for analysis to four separate analytical laboratories as blind controls for organic rich sedimentary rock samples being analyzed from the Red Dog mine area in Alaska. The samples were analyzed for stable isotopes of carbon (delta13Cncc) and nitrogen (delta15N), percent non-carbonate carbon (Wt % Cncc) and percent nitrogen (Wt % N). SDO-1, collected from the Huron Member of the Ohio Shale, near Morehead, Kentucky, and SGR-1, collected from the Mahogany zone of the Green River Formation are petroleum source rocks used as reference materials for chemical analyses of sedimentary rocks. PACS-2 is modern marine sediment collected from the Esquimalt, British Columbia harbor. The results presented in this study are, with the exceptions noted below, the first published for these reference materials. There are published information values for the elemental concentrations of 'organic' carbon (Wt % Corg measured range is 8.98 - 10.4) and nitrogen (Wt % Ntot 0.347 with SD 0.043) only for SDO-1. The suggested values presented here should be considered 'information values' as defined by the NRCC Institute for National Measurement Reference Materials and should be useful for the analysis of 13C, 15N, C and N in organic material in sedimentary rocks.
Chemical immobilization of Pb, Cu, and Cd by phosphate materials and calcium carbonate in contaminated soils.

PubMed

Huang, Guoyong; Su, Xiaojuan; Rizwan, Muhammad Shahid; Zhu, Yifei; Hu, Hongqing

2016-08-01

Soil contamination with toxic metals has increasingly become a global concern over the past few decades. Phosphate and carbonate compounds are good passivation materials for Pb immobilization, while the effect of phosphate and carbonate on the immobilization of multiple heavy metals (Pb, Cu, and Cd) in contaminated soils was seldom investigated. In this study, bone meal (BM), phosphate rock (PR), oxalic acid-activated phosphate rock (APR), super phosphate (SP), and calcium carbonate (CC) were added to the contaminated soils to evaluate the effect of phosphate materials and calcium carbonate on the immobilization of Pb, Cu, and Cd. The results showed that the pH of the treated soils increased 1.3-2.7, except SP which decreased 0.5 at most. Compared to the control treatment, all phosphates and calcium carbonate added to the polluted soils increased the fraction of residual metals, and the application of APR, PR, BM, and CC significantly reduced exchangeable and carbonate-bound fraction metals. PR and APR were the most effective for the immobilization of Pb, Cu, and Cd in the soils among these materials. Moreover, the concentrations of all metals in the toxicity characteristic leaching procedure (TCLP) leachate decreased with increasing amounts of amendments, and the concentrations of Pb in the TCLP leachate for soils treated with PR and APR were below the nonhazardous regulatory limit of 5 mg L(-1) (US Environmental Protection Agency). Based on our results, phosphate rock and oxalic acid-activated phosphate rock are effective in the immobilization of multiple metals by reducing their mobility in the co-contaminated soils.
Fluid-rock reactions in an evaporitic melange, Permian Haselgebirge, Austrian Alps

USGS Publications Warehouse

Spotl, C.; Longstaffe, F.J.; Ramseyer, K.; Kunk, Michael J.; Wiesheu, R.

1998-01-01

Tectonically isolated blocks of carbonate rocks present within the anhydritic Haselgebirge melange of the Northern Calcareous Alps record a complex history of deformation and associated deep-burial diagenetic to very low-grade metamorphic reactions. Fluids were hot (up to ~ 250 ??C) and reducing brines charged with carbon dioxide. Individual carbonate outcrops within the melange record different regimes of brine-rock reactions, ranging from pervasive dolomite recrystallization to dedolomitization. Early diagenetic features in these carbonates were almost entirely obliterated. Matrix dolomite alteration was related to thermochemical sulphate reduction (TSR) recognized by the replacement of anhydrite by calcite + pyrite ?? native sulphur. Pyrite associated with TSR is coarsely crystalline and characterized by a small sulphur isotope fractionation relative to the precursor Permian anhydrite. Carbonates associated with TSR show low Fe/Mn ratios reflecting rapid reaction of ferrous iron during sulphide precipitation. As a result, TSR-related dolomite and calcite typically show bright Mn(II)-activated cathodoluminescence in contrast to the dull cathodoluminescence of many (ferroan) carbonate cements in other deep-burial settings. In addition to carbonates and sulphides, silicates formed closely related to TSR, including quartz, K-feldspar, albite and K-mica. 40Ar/39Ar analysis of authigenic K-feldspar yielded mostly disturbed step-heating spectra which suggest variable cooling through the argon retention interval for microcline during the Late Jurassic. This timing coincides with the recently recognized subduction and closure of the Meliata-Hallstatt ocean to the south of the Northern Calcareous Alps and strongly suggests that the observed deep-burial fluid-rock reactions were related to Jurassic deformation and melange formation of these Permian evaporites.
Earth Observations taken by the Expedition 18 Crew

NASA Image and Video Library

2008-12-29

ISS018-E-015908 (29 Dec. 2008) --- The Biokovo Range in Croatia is featured in this image photographed by an Expedition 18 crewmember on the International Space Station. The Biokovo Range in Croatia is part of the Dinaric Alps extending northwest-southeast along the coastline of the Adriatic Sea. The Range itself is the location of a national park; the nearby city of Makarska, located between the mountains and the sea, is a popular tourist destination. The highest peak in the Biokovo Range, Sveti Jure (1762 meters above sea level), is reachable by road or hiking. The Range is comprised mainly of Mesozoic age carbonate rocks ? primarily limestone, a sedimentary rock type rich in calcium carbonate ? deposited in relatively warm, shallow waters. Later tectonic processes uplifted and exposed the carbonate rocks to erosion ? leading to a distinctive geological surface known as karst topography. Karst topography originates due to the chemical erosion of carbonate rocks by acids formed in surface and subsurface water; as the rock is dissolved, underground networks of drainages and caves form. As more underground void space develops through time, the overlaying rock and soil collapses to form a variety of landforms including sinkholes, blind valleys, and towers. In the Biokovo Range, much of the karst surface has a pitted appearance, made easily visible by early morning light in this astronaut photograph. The pitted appearance is produced by numerous circular or semi-circular collapse valleys known locally as vrtace. While this image captures Sveti Jure covered with snow, there are no glaciers or ice fields in the Biokovo Range.
Geological evolution of the Iraqi Mesopotamia Foredeep, inner platform and near surroundings of the Arabian Plate

NASA Astrophysics Data System (ADS)

Sissakian, Varoujan K.

2013-08-01

The Iraqi territory could be divided into four main tectonic zones; each one has its own characteristics concerning type of the rocks, their age, thickness and structural evolution. These four zones are: (1) Inner Platform (stable shelf), (2) Outer Platform (unstable shelf), (3) Shalair Zone (Terrain), and (4) Zagros Suture Zone. The first two zones of the Arabian Plate lack any kind of metamorphism and volcanism. The Iraqi territory is located in the extreme northeastern part of the Arabian Plate, which is colliding with the Eurasian (Iranian) Plate. This collision has developed a foreland basin that includes: (1) Imbricate Zone, (2) High Folded Zone, (3) Low Folded Zone and (4) Mesopotamia Foredeep. The Mesopotamia Foredeep, in Iraq includes the Mesopotamia Plain and the Jazira Plain; it is less tectonically disturbed as compared to the Imbricate, High Folded and Low Folded Zones. Quaternary alluvial sediments of the Tigris and Euphrates Rivers and their tributaries as well as distributaries cover the central and southeastern parts of the Foredeep totally; it is called the Mesopotamian Flood Plain. The extension of the Mesopotamia Plain towards northwest however, is called the Jazira Plain, which is covered by Miocene rocks. The Mesopotamia Foredeep is represented by thick sedimentary sequence, which thickens northwestwards including synrift sediments; especially of Late Cretaceous age, whereas on surface the Quaternary sediments thicken southeastwards. The depth of the basement also changes from 8 km, in the west to 14 km, in the Iraqi-Iranian boarders towards southeast. The anticlinal structures have N-S trend, in the extreme southern part of the Mesopotamia Foredeep and extends northwards until the Latitude 32°N, within the Jazira Plain, there they change their trends to NW-SE, and then to E-W trend. The Mesozoic sequence is almost without any significant break, with increase in thickness from the west to the east, attaining 5 km. The sequence forms the main source and reservoir rocks in the central and southern parts of Iraq. The Cenozoic sequence consists of Paleogene open marine carbonates, which grades upwards into Neogene lagoonal marine; of Early Miocene and evaporitic rocks; of Middle Miocene age, followed by thick molasses of continental clastics that attain 3500 m in thickness; starting from Late Miocene. The Quaternary sediments are very well developed in the Mesopotamia Plain and they thicken southwards to reach about 180 m near Basra city; in the extreme southeastern part of Iraq. The Iraqi Inner Platform (stable shelf) is a part of the Arabian Plate, being less affected by tectonic disturbances; it covers the area due to south and west of the Euphrates River. The main tectonic feature in this zone that had affected on the geology of the area is the Rutbah Uplift; with less extent is the Ga'ara High. The oldest exposed rocks within the Inner Platform belong to Ga'ara Formation of Permian age; it is exposed only in the Ga'ara Depression. The Permian rocks are overlain by Late Triassic rocks; represented by Mulussa and Zor Hauran formations, both of marine carbonates with marl intercalations. The whole Triassic rocks are absent west, north and east of Ga'ara Depression. Jurassic rocks, represented by five sedimentary cycles, overlie the Triassic rocks. Each cycle consists of clastic rocks overlain by carbonates, being all of marine sediments; whereas the last one (Late Jurassic) consists of marine carbonates only. All the five formations are separated from each other by unconformable contacts. Cretaceous rocks, represented by seven sedimentary cycles, overlie the Jurassic rocks. Marine clastics overlain by marine carbonates. Followed upwards (Late Cretaceous) by continental clastics overlain by marine carbonates; then followed by marine carbonates with marl intercalations, and finally by marine clastics overlain by carbonates; representing the last three cycles, respectively. The Paleocene rocks form narrow belt west of the Ga'ara Depression, represented by Early-Late Paleocene phosphatic facies, which is well developed east of Rutbah Uplift and extends eastwards in the Foredeep. Eocene rocks; west of Rutbah Uplift are represented by marine carbonates that has wide aerial coverage in south Iraq. Locally, east of Rutbah Uplift unconformable contacts are recorded between Early, Middle and Late Eocene rocks. During Oligocene, in the eastern margin of the Inner Platform, the Outer Platform was uplifted causing very narrow depositional Oligocene basin. Therefore, very restricted exposures are present in the northern part of the Inner Platform (north of Ga'ara Depression), represented by reef, forereef sediments of some Oligocene formations. The Miocene rocks have no exposures west of Rutbah Uplift, but north and northwestwards are widely exposed represented by Early Miocene of marine carbonates with marl intercalations. Very locally, Early Miocene deltaic clastics and carbonates, are interfingering with the marine carbonates. The last marine open sea sediments, locally with reef, represent the Middle Miocene rocks and fore reef facies that interfingers with evaporates along the northern part of Abu Jir Fault Zone, which is believed to be the reason for the restriction of the closed lagoons; in the area. During Late Miocene, the continental phase started in Iraq due to the closure of the Neo-Tethys and collision of the Sanandaj Zone with the Arabian Plate. The continental sediments consist of fine clastics. The Late Miocene - Middle Pliocene sediments were not deposited in the Inner Platform. The Pliocene-Pleistocene sediments are represented by cyclic sediments of conglomeratic sandstone overlain by fresh water limestone, and by pebbly sandstone. The Quaternary sediments are poorly developed in the Inner Platform. Terraces of Euphrates River and those of main valleys represent pleistocene sediments. Flood plain of the Euphrates River and those of large valleys represent Holocene sediments. Residual soil is developed, widely in the western part of Iraq, within the western marginal part of the Inner Platform.
Long-term effects of CO2 on the mechanical behaviour of faults - a study of samples from a natural CO2 analogue (Entrada Sandstone, Utah, USA)

NASA Astrophysics Data System (ADS)

Bakker, E.; Hangx, S.; Spiers, C. J.

2012-12-01

CO2 capture followed by storage in depleted oil and gas reservoirs is currently seen as one of the most promising CO2-mitigation strategies. An important issue in relation to long-term CO2 storage is the prediction of the effects of fluid-rock interaction on the mechanical integrity and sealing capacity of the reservoir-seal system, on timescales of the order of 103 or 104 years. However, the assumed chemical interactions in the rock/CO2/brine system are slow, so that their long-term effects on rock composition, microstructure, mechanical properties and transport properties cannot be reproduced in laboratory experiments. One way to address this is to study the effects of reactions in natural CO2 reservoirs, using a so-called natural analogue approach. We tackled the question of how reactions characterizing natural CO2 fields affect fault friction, fault reactivation potential and seismic vs. aseismic slip stability, as well as transmissivity evolution during and after fault reactivation. Simulated fault gouges were prepared by crushing material obtained from surface outcrops of the Entrada Sandstone, a locally CO2-bearing formation forming an analogue field under the Colorado Plateau, Utah, USA . We used three types of starting material: 1) CO2 unaffected (unbleached) samples consisting mainly of quartz and feldspar, 2) "bleached" samples, and 3) heavily cemented/altered fault rock containing a high percentage of carbonates (> 40 wt%). The latter two were altered as a result of interaction with CO2-rich fluids over geological time. We performed triaxial direct shear experiments on these materials at room temperature under nominally dry conditions, at normal stresses up to 90 MPa and shear velocities of 0.22 -10.9 μm/s. The results of the experiments yielded friction coefficients (μ= τ/σn) of 0.55-0.85 for unbleached sandstone gouge and 0.45-0.80 for bleached material, while the fault material showed systematically higher friction coefficients (0.60-0.95). All simulated gouges showed a decrease in friction coefficient of 20-30% with increasing normal stress up to 90 MPa, with almost all samples showing velocity-strengthening (stable) slip behaviour. Permeability measurements show only minor changes during shear. Overall, our results demonstrated that higher (CO2-related) carbonate content leads to higher frictional strength and increased velocity strengthening (slip stability), notably at low normal stresses. However, preliminary results recently obtained at elevated temperatures show that carbonate-rich samples show velocity-weakening behaviour at 100°C, which is in line with previous studies on pure carbonates. A natural analogue from The Netherlands shows similar results for the chemical alteration of reservoir rock by the presence of naturally long-term stored CO2.
Spectrophotometric determination of fluorine in silicate rocks

USGS Publications Warehouse

Peck, L.C.; Smith, V.C.

1964-01-01

The rock powder is sintered with a sodium carbonate flux containing zinc oxide and magnesium carbonate, the sinter-cake leached with water and the resulting solution filtered. Fluorine is separated from the acidified filtrate by steam distillation and determined spectrophotometrically by means of a zirconium-SPADNS reagent. If a multiple-unit distillation apparatus is used, 12 determinations can be completed per man-day. ?? 1964.
Hydrogeologic and geospatial data for the assesment of focused recharge to the Carbonate-Rock Aquifer in Genesee County, New York

USGS Publications Warehouse

Reddy, James E.; Kappel, William M.

2010-01-01

Existing hydrogeologic and geospatial data useful for the assessment of focused recharge to the carbonate-rock aquifer in the central part of Genesee County, NY, were compiled from numerous local, State, and Federal agency sources. Data sources utilized in this pilot study include available geospatial datasets from Federal and State agencies, interviews with local highway departments and the Genesee County Soil and Water Conservation District, and an initial assessment of karst features through the analysis of ortho-photographs, with minimal field verification. The compiled information is presented in a series of county-wide and quadrangle maps. The county-wide maps present generalized hydrogeologic conditions including distribution of geologic units, major faults, and karst features, and bedrock-surface and water-table configurations. Ten sets of quadrangle maps of the area that overlies the carbonate-rock aquifer present more detailed and additional information including distribution of bedrock outcrops, thin and (or) permeable soils, and karst features such as sinkholes and swallets. Water-resource managers can utilize the information summarized in this report as a guide to their assessment of focused recharge to, and the potential for surface contaminants to reach the carbonate-rock aquifer.
The Early Mesozoic volcanic arc of western North America in northeastern Mexico

NASA Astrophysics Data System (ADS)

Barboza-Gudiño, José Rafael; Orozco-Esquivel, María Teresa; Gómez-Anguiano, Martín; Zavala-Monsiváis, Aurora

2008-02-01

Volcanic successions underlying clastic and carbonate marine rocks of the Oxfordian-Kimmeridgian Zuloaga Group in northeastern Mexico have been attributed to magmatic arcs of Permo-Triassic and Early Jurassic ages. This work provides stratigraphic, petrographic geochronological, and geochemical data to characterize pre-Oxfordian volcanic rocks outcropping in seven localities in northeastern Mexico. Field observations show that the volcanic units overlie Paleozoic metamorphic rocks (Granjeno schist) or Triassic marine strata (Zacatecas Formation) and intrude Triassic redbeds or are partly interbedded with Lower Jurassic redbeds (Huizachal Group). The volcanic rocks include rhyolitic and rhyodacitic domes and dikes, basaltic to andesitic lava flows and breccias, and andesitic to rhyolitic pyroclastic rocks, including breccias, lapilli, and ashflow tuffs that range from welded to unwelded. Lower-Middle Jurassic ages (U/Pb in zircon) have been reported from only two studied localities (Huizachal Valley, Sierra de Catorce), and other reported ages (Ar/Ar and K-Ar in whole-rock or feldspar) are often reset. This work reports a new U/Pb age in zircon that confirms a Lower Jurassic (193 Ma) age for volcanic rocks exposed in the Aramberri area. The major and trace element contents of samples from the seven localities are typical of calc-alkaline, subduction-related rocks. The new geochronological and geochemical data, coupled with the lithological features and stratigraphic positions, indicate volcanic rocks are part of a continental arc, similar to that represented by the Lower-Middle Jurassic Nazas Formation of Durango and northern Zacatecas. On that basis, the studied volcanic sequences are assigned to the Early Jurassic volcanic arc of western North America.
Removing the effects of metamorphism from the Neoproterozoic carbon isotope record: a case study on Islay, western Scotland

NASA Astrophysics Data System (ADS)

Skelton, Alasdair

2016-04-01

The Port Askaig Formation on Islay, western Scotland is the first discovered tillite (glacial sediment) of Neoproterozoic age. This formation is sandwiched between carbonate rocks which preserve an extreme negative carbon isotope excursion. This so called "Islay anomaly" has been correlated with other such anomalies worldwide and together with the tillites has been cited as evidence of major (worldwide) glaciation events. During subsequent mountain building, this carbonate-tillite- carbonate sequence has been folded, producing a major en-echelon anticlinal fold system. Folding was accompanied by metamorphism at greenschist facies conditions which was, in turn, accompanied by metamorphic fluid flow. Mapping of the δ18O and δ13C values of these carbonate rocks reveals that metamorphic fluids were channelled through the axial region of the anticlinal fold. The metamorphic fluid was found to have a highly negative δ13C value, which was found to be in equilibrium with metamorphosed graphitic mudstones beneath the carbonate-tillite-carbonate sequence. Devolatilisation of these mudstones is therefore a likely source of this metamorphic fluid. Removal of the effects of metamorphic fluid flow on δ13C values recorded by metamorphosed carbonate rocks on Islay allows us to re-evaluate the isotopic evidence used to reconstruct Neoproterozoic climate. We are able to show that extreme negative δ13C values can partly be attributed to metamorphic fluid flow.
Interaction of Rock Minerals with Carbon Dioxide and Brine: A Hydrothermal Investigation

DOE Office of Scientific and Technical Information (OSTI.GOV)

Sass, Bruce M.; Gupta, Neeraj; Ickes, Jennifer A.

2002-02-02

This paper presents interim results of a feasibility study on carbon dioxide (CO{sub 2}) sequestration in deep saline formations. The focus of the investigation is to examine factors that may affect chemical sequestration of CO{sub 2} in deep saline formations. Findings of the first phase of this investigation were presented in a topical report (Sass et al., 1999a). Preliminary results of the second phase, now underway, have been reported elsewhere (Sass et al., 1999b; 2001). Evaluations of the suitability of Mt. Simon formation for sequestering CO{sub 2} and economic issues are reported by Gupta et al., 1999; 2001; Smith etmore » al., 2001. This study is sponsored by the U.S. Department of Energy's (DOE) National Energy Technology Laboratory (NETL) under a Novel Concepts project grant. The overall objectives of Phase II experiments were to determine: (1) the potential for long-term sequestration of CO{sub 2} in deep, regional host rock formations; and (2) the effectiveness of overlying caprock as a barrier against upward migration of the injected CO{sub 2}. To meet these goals, experiments were conducted using rock samples from different potential host reservoirs and overlying rocks. In addition, pure mineral samples were used in some experimental runs to investigate specific mineralogical reactions. Due to space limitations, the scope of this paper will be limited to two types of equilibration experiments using pure minerals. Implications for more complex natural systems will be discussed in the report for Phase II being finalized at this time.« less
CUMULATE ROCKS ASSOCIATED WITH CARBONATE ASSIMILATION, HORTAVÆR COMPLEX, NORTH-CENTRAL NORWAY

NASA Astrophysics Data System (ADS)

Barnes, C. G.; Prestvik, T.; Li, Y.

2009-12-01

The Hortavær igneous complex intruded high-grade metamorphic rocks of the Caledonian Helgeland Nappe Complex at ca. 466 Ma. The complex is an unusual mafic-silicic layered intrusion (MASLI) because the principal felsic rock type is syenite and because the syenite formed in situ rather than by deep-seated partial melting of crustal rocks. Magma differentiation in the complex was by assimilation, primarily of calc-silicate rocks and melts with contributions from marble and semi-pelites, plus fractional crystallization. The effect of assimilation of calcite-rich rocks was to enhance stability of fassaitic clinopyroxene at the expense of olivine, which resulted in alkali-rich residual melts and lowering of silica activity. This combination of MASLI-style emplacement and carbonate assimilation produced three types of cumulate rocks: (1) Syenitic cumulates formed by liquid-crystal separation. As sheets of mafic magma were loaded on crystal-rich syenitic magma, residual liquid was expelled, penetrating the overlying mafic sheets in flame structures, and leaving a cumulate syenite. (2) Reaction cumulates. Carbonate assimilation, illustrated by a simple assimilation reaction: olivine + calcite + melt = clinopyroxene + CO2 resulted in cpx-rich cumulates such as clinopyroxenite, gabbro, and mela-monzodiorite, many of which contain igneous calcite. (3) Magmatic skarns. Calc-silicate host rocks underwent partial melting during assimilation, yielding a Ca-rich melt as the principal assimilated material and permitting extensive reaction with surrounding magma to form Kspar + cpx + garnet-rich ‘cumulate’ rocks. Cumulate types (2) and (3) do not reflect traditional views of cumulate rocks but instead result from a series of melt-present discontinuous (peritectic) reactions and partial melting of calc-silicate xenoliths. In the Hortavær complex, such cumulates are evident because of the distinctive peritectic cumulate assemblages. It is unclear whether assimilation of ‘normal’ silicate rocks results in peritectic assemblages, or whether they could be identified as such if they exist.
Carboniferous and older carbonate rocks: Lithofacies, extent, and reservoir quality: Chapter CC in The oil and gas resource potential of the Arctic National Wildlife Refuge 1002 area, Alaska

USGS Publications Warehouse

Dumoulin, Julie A.

1999-01-01

Carboniferous and older carbonate rocks are potential hydrocarbon reservoir facies for four plays in the 1002 area of the Arctic National Wildlife Refuge. These rocks include several units in the pre-Carboniferous basement and the Carboniferous Lisburne Group. Data from exploratory wells west of the 1002 area, outcrops south of the 1002 area, seismic lines, and well logs are synthesized herein to infer carbonate lithofacies, extent, and reservoir character beneath the northeastern Arctic coastal plain.A chiefly shallow-water basement carbonate succession of Late Proterozoic through Early Devonian age (Katakturuk Dolomite, Nanook Limestone, and Mount Copleston Limestone) is interpreted to be present beneath much of the south-central 1002 area; it reaches 3,700 m thick in outcrop and is the primary reservoir for the Deformed Franklinian Play. A more heterogeneous lithologic assemblage of uncertain age forms basement in the northwestern part of the 1002 area; well data define three subunits that contain carbonate intervals 5- 50 m thick. These strata are prospective reservoirs for the Undeformed Franklinian Play and could also be reservoirs for the Niguanak- Aurora Play. Regional lithologic correlations suggest a Cambrian-Late Proterozoic(?) age for subunits one and two, and a slightly younger, later Cambrian-Silurian age for subunit three. Seismic and well data indicate that subunit one overlies subunit two and is overlain by subunit three. The Mississippian and Pennsylvanian Lisburne Group, a predominantly carbonate platform succession as much as 1 km thick, is projected beneath the southernmost part of the 1002 area and is a potential reservoir for the Ellesmerian Thrust-belt and Niguanak-Aurora Plays.Carbonate rocks in the 1002 area probably retain little primary porosity but may have locally well developed secondary porosity. Measured reservoir parameters in basement carbonate strata are low (porosity generally ≤ 5%; permeability ≤ 0.2 md) but drill-stem tests found locally reasonable flow rates (4,220-4,800 bpd) and, in the Flaxman Island area, recovered gas and condensate from these rocks. The Lisburne Group has produced up to 50,000 bbl of oil/ day from the Lisburne field at Prudhoe Bay. Reservoir parameters of the Lisburne in northeastern Alaska range from low (porosities ≤ 5% in most limestones) to good (porosities average 6.5-10% in some dolostones). Reservoir quality in Carboniferous and older carbonate strata in the 1002 area should be greatest where these rocks are highly fractured and (or) truncated by the Lower Cretaceous Unconformity.
The Formation of Fe/Mg Smectite Under Mildly Acidic Conditions on Early Mars

NASA Technical Reports Server (NTRS)

Sutter, Brad; Golden, D. C.; Ming, Douglas W.; Niles, P. B.

2011-01-01

The detection of Fe/Mg smectites and carbonate in Noachian and early Hesperian terrain of Mars has been used to suggest that neutral to mildly alkaline conditions prevailed during the early history of Mars. However, if early Mars was neutral to moderately alkaline with a denser CO2 atmosphere than today, then large carbonates deposits should be more widely detected in Noachian terrain. The critical question is: Why have so few carbonate deposits been detected compared to Fe/Mg smectites? We suggest that Fe/Mg smectites on early Mars formed under mildly acidic conditions, which would inhibit the extensive formation of carbonate deposits. The goal of this work is to evaluate the formation of Fe/Mg smectites under mildly acidic conditions. The stability of smectites under mildly acidic conditions is attributed to elevated Fe/Mg activities that inhibit smectite dissolution. Beidelite and saponite have been shown to form from hydrothermal alteration of basaltic glass at pH 3.5-4.0 in seawater solutions. Nontronite is also known to be stable in mildly acidic systems associated with mafic and ultramafic rock. Nontronite was shown to form in acid sulfate soils in the Bangkok Plain, Thailand due to oxidation of Fe-sulfides that transformed saponite to nontronite. Smectite is known to transform to kaolinite in naturally acid soils due to selective leaching of Mg. However, if Mg removal is limited, then based on equilibrium relationships, the dissolution of smectite should be minimized. If Fe and Mg solution activities are sufficiently high, such as might be found in a low water/rock ratio system that is poorly drained, smectite could form and remain stable under mildly acidic conditions on Mars. The sources of mild acidity on early Mars includes elevated atmospheric CO2 levels, Fe-hydrolysis reactions, and the presence of volcanic SO2 aerosols. Equilibrium calculations dictate that water equilibrated with an early Mars CO2 atmosphere at 1 to 4 bar yields a pH of 3.6 to 3.9. Fe hydrolysis reactions on Mars is another source of protons that would have contributed to acidity. The presence of SO2 from volcanic processes could also have contributed to geochemical acidification. These sources of acidity competed with base-forming cations that resulted in mildly acidic solutions that were not favorable for carbonate formation but may have allowed for Fe/Mg smectite formation. Noachian to early Hesperian Mars could have been mildly acidic, allowing Fe/Mg smectite formation but preventing widespread carbonate deposition. This paradigm shift from an early Mars that was neutral-alkaline to mildly acidic may possibly explain why there is a disparity between the occurrence of carbonate and Fe/Mg smectites. Potential microbiological activity would not be eliminated under a mildly acidic Mars; however, there could be tighter constraints as to the type and species of microbiology that could exist.
Stress path dependent hydromechanical behaviour of heterogeneous carbonate rock

NASA Astrophysics Data System (ADS)

Gland, N.; Dautriat, J.; Dimanov, A.; Raphanel, J.

2010-06-01

The influence of stress paths, representative of reservoir conditions, on the hydromechanical behavior of a moderately heterogeneous carbonate has been investigated. Multiscale structural heterogeneities, common for instance in carbonate rocks, can strongly alter the mechanical response and significantly influence the evolution of flow properties with stress. Using a triaxial cell, the permeability evolutions during compression and the effects of brittle (fracture) and plastic (pore collapse) deformations at yield, were measured. A strong scattering was observed on the mechanical response both in term of compressibility and failure threshold. Using the porosity scaling predicted by an adapted effective medium theory (based on crack growth under Hertzian contact), we have rescaled the critical pressures by the normalized porosity deviation. This procedure reduces efficiently the scattering, revealing in the framework of proportional stress path loading, a linear relation between the critical pressures and the stress path parameter through all the deformation regimes. It leads to a new formulation for the critical state envelope in the 'mean stress, deviatoric stress' diagram. The attractive feature of this new yield envelope formulation relies on the fact that only the two most common different mechanical tests 'Uniaxial Compression' and 'Hydrostatic Compression', are needed to define entirely the yield envelope. Volumic strains and normalized permeabilities are finally mapped in the stresses diagram and correlated.
Collision-induced tectonism along the northwestern margin of the Indian subcontinent as recorded in the Upper Paleocene to Middle Eocene strata of central Pakistan (Kirthar and Sulaiman Ranges)

USGS Publications Warehouse

Warwick, Peter D.; Johnson, Edward A.; Khan, Intizar H.

1998-01-01

Outcrop data from the Upper Paleocene to Middle Eocene Ghazij Formation of central Pakistan provide information about the depositional environments, source areas, and paleogeographic and tectonic settings along the northwestern margin of the Indian subcontinent during the closing of the Tethys Ocean. In this region, in the lower part of the exposed stratigraphic sequence, are various marine carbonate-shelf deposits (Jurassic to Upper Paleocene). Overlying these strata is the Ghazij, which consists of marine mudstone (lower part), paralic sandstone and mudstone (middle part), and terrestrial mudstone and conglomerate (upper part). Petrographic examination of sandstone samples from the middle and upper parts reveals that rock fragments of the underlying carbonate-shelf deposits are dominant; also present are volcanic rock fragments and chromite grains. Paleocurrent measurements from the middle and upper parts suggest that source areas were located northwest of the study area. We postulate that the source areas were uplifted by the collision of the subcontinent with a landmass during the final stages of the closing of the Tethys Ocean. Middle Eocene carbonate-shelf deposits that overlie the Ghazij record a return to marine conditions prior to the Miocene to Pleistocene sediment influx denoting the main collision with Eurasia.
The Kingak shale of northern Alaska-regional variations in organic geochemical properties and petroleum source rock quality

USGS Publications Warehouse

Magoon, L.B.; Claypool, G.E.

1984-01-01

The Kingak Shale, a thick widespread rock unit in northern Alaska that ranges in age from Early Jurassic through Early Cretaceous, has adequate to good oil source rock potential. This lenticular-shaped rock unit is as much as 1200 m thick near the Jurassic shelf edge, where its present-day burial depth is about 5000 m. Kingak sediment, transported in a southerly direction, was deposited on the then marine continental shelf. The rock unit is predominantly dark gray Shale with some interbeds of thick sandstone and siltstone. The thermal maturity of organic matter in the Kingak Shale ranges from immature (2.0%R0) in the Colville basin toward the south. Its organic carbon and hydrogen contents are highest in the eastern part of northern Alaska south of and around the Kuparuk and Prudhoe Bay oil fields. Carbon isotope data of oils and rock extracts indicate that the Kingak Shale is a source of some North Slope oil, but is probably not the major source. ?? 1984.
A Lithospheric Origin for the Elk Creek Carbonatite Complex, SE Nebraska?

NASA Astrophysics Data System (ADS)

Farmer, G. L.

2015-12-01

The Elk Creek carbonatite complex in southeastern Nebraska is part of a widespread Cambrian-Ordovician alkali igneous event that affected much of North America during and after the break-up of the Rodinian supercontinent. We conducted whole rock and mineral Nd, Sr, Pb and Hf isotopic analyses of drill cores obtained from this complex in order to assess the source regions of the parental carbonatite magma. Low precision laser ablation U-Pb age determinations from individual zircon grains separated from carbonate-rich "syenites" range from 480 +/- 20 Ma to 540+/- 14 Ma. Whole rock Nd, Sr and Pb isotopic compositions all plot on Cambrian (~550 Ma) isochrons, implying that the carbonatites crystallized from melts with homogeneous radiogenic isotopic compositions. Initial ɛNd and ɛHf are well defined at ~+2 and ~0, respectively, while initial 87Sr/86Sr values are more variable and range from 0.7028 to 0.7058. The contemporaneously emplaced State Line kimberlites in the Front Range of north central Colorado share the same Nd and Sr isotopic compositions imply that sources of these rocks were similar and geographically widespread. Overall, the isotopic compositions are those expected from "Group 1" alkaline igneous rocks, usually interpreted as derivates from the sublithospheric mantle. Cretaceous-Tertiary alkaline rocks in North America generally belong to "Group 1" and may have originated in this fashion (Genet et al., 2014, Earth Planet. Sci. Lett.). An alternative possibility is that the Cambrian-Ordovician carbonatites and kimberlites were derived from underlying, carbonated portions of the lithospheric mantle that formed after the original stabilization of the latter in the Paleoproterozoic. Nd and Hf depleted mantle model ages for the Elk Creek and State Line alkaline rocks range from ~0.8 Ga to ~1.1 Ga and allow the possibility that both sets of intrusive rocks represent melting of mantle metasomatized either during or after the assembly of Rodinia. Widespread thinning and heating of the metasomatized mantle during the subsequent breakup of Rodinia could have led to the widespread kimberlite and carbonatite magmatism observed in North America during the Cambrian.
Methanogenic calcite, 13C-depleted bivalve shells, and gas hydrate from a mud volcano offshore southern California

USGS Publications Warehouse

Hein, J.R.; Normark, W.R.; McIntyre, B.R.; Lorenson, T.D.; Powell, C.L.

2006-01-01

Methane and hydrogen sulfide vent from a cold seep above a shallowly buried methane hydrate in a mud volcano located 24 km offshore southern California in?? 800 m of water. Bivalves, authigenic calcite, and methane hydrate were recovered in a 2.1 m piston core. Aragonite shells of two bivalve species are unusually depleted in 13C (to -91??? ??13C), the most 13C-depleted shells of marine macrofauna yet discovered. Carbon isotopes for both living and dead specimens indicate that they used, in part, carbon derived from anaerobically oxidized methane to construct their shells. The ??13C values are highly variable, but most are within the range -12??? to -91???. This variability may be diagnostic for identifying cold-seep-hydrate systems in the geologic record. Authigenic calcite is abundant in the cores down to ???1.5 m subbottom, the top of the methane hydrate. The calcite is depleted in 13C (??13C = -46??? to -58???), indicating that carbon produced by anaerobically oxidized methane is the main source of the calcite. Methane sources include a geologic hydrocarbon reservoir from Miocene source rocks, and biogenic and thermogenic degradation of organic matter in basin sediments. Oxygen isotopes indicate that most calcite formed out of isotopic equilibrium with ambient bottom water, under the influence of gas hydrate dissociation and strong methane flux. High metal content in the mud volcano sediment indicates leaching of basement rocks by fluid circulating along an underlying fault, which also allows for a high flux of fossil methane. ?? 2006 Geological Society of America.

Manganese and iron geochemistry in sediments underlying the redox-stratified Fayetteville Green Lake

NASA Astrophysics Data System (ADS)

Herndon, Elizabeth M.; Havig, Jeff R.; Singer, David M.; McCormick, Michael L.; Kump, Lee R.

2018-06-01

Manganese and iron are redox-sensitive elements that yield clues about biogeochemistry and redox conditions both in modern environments and in the geologic past. Here, we investigated Mn and Fe-bearing minerals preserved in basin sediments underlying Fayetteville Green Lake, a redox-stratified lake that serves as a geochemical analogue for Paleoproterozoic oceans. Synchrotron-source microprobe techniques (μXRF, μXANES, and μXRD) and bulk geochemical analyses were used to examine the microscale distribution and speciation of Mn, Fe, and S as a function of depth in the top 48 cm of anoxic lake sediments. Manganese was primarily associated with calcite grains as a manganese-rich carbonate that precipitated in the chemocline of the water column and settled through the euxinic basin to collect in lake sediments. Iron was preserved in framboidal iron sulfides that precipitated in euxinic bottom waters and underwent transformation to pyrite and marcasite in the sediments. Previous studies attribute the formation of manganese-rich carbonates to the diagenetic alteration of manganese oxides deposited in basins underlying oxygenated water. Our study challenges this paradigm by providing evidence that Mn-bearing carbonates form in the water column and accumulate in sediments below anoxic waters. Consequently, manganoan carbonates preserved in the rock record do not necessarily denote the presence of oxygenated bottom waters in ocean basins.
Karst Lands: The dissolution of carbonate rock produces unique landscapes and poses significant hydrological and environmental concerns

DOE Office of Scientific and Technical Information (OSTI.GOV)

White, W.B.; Culver, D.C.; Herman, J.S.

1995-09-01

Karst lands are produced by the action of water on soluble rocks, a process among the most dynamic of all erosive forces that counterbalance the uplifting forces of tectonics. The dissolution of carbonate rock, primarily limestone and dolomite, produces unique landscapes and poses significant hydrological and environmental concerns. The major topic areas discussed in this article include the following: processes that form karst; karst drainage basins; discharge from karst aquifers; caves as paleoclimatic recorders; caves as ecosystems; water issues in karst regions; and sinkholes, soil piping and subsidence. 20 refs., 9 figs.
Dolomitization of felsic volcaniclastic rocks in continental strata: A study from the Lower Cretaceous of the A'nan Sag in Er'lian Basin, China

NASA Astrophysics Data System (ADS)

Zhu, Shifa; Yue, Hui; Zhu, Xiaomin; Sun, Shuyang; Wei, Wei; Liu, Xin; Jia, Ye

2017-05-01

Dolomitization of fine-grained volcaniclastic rocks is common in the Lower Cretaceous of the A'nan Sag in the Er'lian Basin of China. Analysis of core samples shows that the organic-rich volcaniclastic rocks are mainly composed of reworked felsic volcanic materials and terrigenous clay minerals. The fine-grained volcaniclastic rocks can be divided into four types: volcaniclastic rocks without carbonatization, volcaniclastic rocks with ferroan dolomites, dolomitized and calcified volcaniclastic rocks, and calcified volcaniclastic rocks. The parent rocks of the volcaniclastic rocks have high silicon and potassium contents and low iron and magnesium contents, and are probably felsic magma of the calc-alkaline series. The average values of δ13CPDB of the carbonate minerals are about 3.13‰; the average values of δ18OPDB are about - 16.74‰. The compositions of C and O isotopes are probably influenced by bacterial methanogenesis. Iron, magnesium, and calcium are probably derived from illitization of terrigenous smectite. A model for dolomitization of felsic volcaniclastic rock is proposed, including three stages: 1) mixed sedimentation and bacterial methanogenesis (< 75 °C); 2) transformation of clay minerals (> 70 °C) and dolomitization (75 to 97 °C); and 3) dissolution. Late dissolution of authigenic carbonate minerals, creating abundant secondary pores, is significant for hydrocarbon accumulation.
High voltage stable liquid electrolytes for Li 1+ xMn 2O 4/carbon rocking-chair lithium batteries

NASA Astrophysics Data System (ADS)

Guyomard, D.; Tarascon, J. M.

A high voltage oxidation-resistant electrolyte is required for Li 1+ xMn 2O 4/carbon rocking-chair cells that need to be charged up to a voltage higher than 4.3 V. Many electrolyte compositions have been tested for their ability to resist to high voltages on Li 1+ xMn 2O 4 electrodes and their ability to maintain high ionic conductivity in a wide temperature range. This survey allowed us to select new electrolyte compositions in the system dimethyl carbonate (DMC) + ethylene carbonate (EC) + lithium hexafluorophosphate (LiPF 6) that are kinetically stable up to almost 5 V versus lithium at 55 °C on Li 1+ xMn 2O 4 electrodes. Low rate potentiostatic experiments, coupled with coulombmetric measurements in the 4.25-5.1 V range, allowed to select the following compositions: (DMC + EC) (1:2) + 1 M LiPF 6 and (DMC + EC) (2:1) + 1.5 M LiPF 6 as the best. These compositions have been used in practical Li 1+ xMn 2O 4/carbon rocking-chair batteries and show better performance in terms of cycle life and self-discharge over a wider temperature range. They are compatible with rocking-chair batteries based on LiCoO 2 and LiNiO 2 as well.
Chemical features of soils in a natural forest of West Hungary

NASA Astrophysics Data System (ADS)

Hofmann, Eszter; Bidló, András

2015-04-01

The present research focuses on the chemical results of soils formed on miocene carbonate rocks in a natural forest of West Hungary. Soil profiles derived from the Szárhalom Forest, located near the Lake Fertő, next to the city of Sopron. Six soil profiles were opened and analysed in this area. In the field the following physical parameters were evaluated from the soil profiles: transition, structure, compactness, roots, skeletal percent, colour, physical assortment, concretion and soil defect. Laboratory analysis involved the measurement of acidity, particle distribution, carbonated lime content, humus content, ammonium lactate-acetic acid soluble phosphorus- and potassium content, potassium chloride soluble calcium- and magnesium content, ethylene-diamine-tetraacetic-acid (EDTA) and diethylene-triamine-pentaacetic-acid (DTPA) soluble copper-, iron-, manganese- and zinc contents. These soils formed under a hornbeam-oak forest climate mainly and under a beech forest climate diffusely. The location and climate of the sites forms a basis of the comparison of the soils with similar base rock. The formation of the acidic and humus-rich upper layer of the soil profiles is influenced by the mineral composition and the weathering of the rocks. X-ray diffraction (Philips P W3710/PW1050 type X-ray diffractometer), thermoanalytical measurements (Mettler Toledo TGA/DSC 1 type thermogravimeter) and ICP-OES (Thermo Scientific iCAP 7000 Series) were also carried out to determine the mineral composition of the soils and the content of heavy metals. The soil samples were collected with both traditional and undisturbed (using the Kubiena box) sampling methods to enable further micromorphological investigations as well. The research is supported by the "Agroclimate-2" (VKSZ_12-1-2013-0034) joint EU-national research project. Key words: Natural forest, Miocene limestone, Mineral composition, Thermal analysis, Micromorphology
In vitro receptivity of carbonate rocks to endolithic lichen-forming aposymbionts.

PubMed

Favero-Longo, Sergio E; Borghi, Alessandro; Tretiach, Mauro; Piervittori, Rosanna

2009-10-01

Sterile cultured isolates of lichen-forming aposymbionts have not yet been used to investigate lichen-rock interactions under controlled conditions. In this study mycobionts and photobiont of the endolithic lichens Bagliettoa baldensis and Bagliettoa marmorea were isolated and inoculated with coupons of one limestone and four marbles commonly employed in the Cultural Heritage framework. After one year of incubation, microscopic observations of polished cross-sections were performed to verify if the typical colonization patterns observed in the field may be reproduced in vitro and to evaluate the receptivity of the five lithotypes to endolithic lichens. The mycobionts of the two species developed both on the surface of and within all the lithotypes, showing different penetration pathways which depend on mineralogical and structural features and highlight different receptivity. By contrast, algae inoculated with the coupons did not penetrate them. Observations suggest that the hyphal penetration along intrinsic discontinuities of rocks is a relatively fast phenomenon when these organisms are generally considered as slow-growing. Samples from limestone outcrops and abandoned marble quarries, colonized by the same species or other representatives of Verrucariaceae, showed penetration pathways intriguingly similar to those reproduced in vitro and highlighted that lichen-driven erosion processes only increase the availability of hyphal passageways after a long-term colonization. These results show that in vitro incubation of sterile cultured lichen-forming ascomycetes with rock coupons is a practicable experimental system to investigate the lichen-rock interactions under controlled conditions and, together with analysis in situ, may support decisions on conservative treatments of historical and cultural significant stone substrata.
Thermodynamic Parameterization of Subduction-Zone Devolatilization and Application to Quantify Carbon Fluxes from Slab

NASA Astrophysics Data System (ADS)

Tian, M.; Katz, R. F.; Rees Jones, D. W.; May, D.

2017-12-01

Compared with other plate-tectonic boundaries, subduction zones (SZ) host the most drastic mechanical, thermal, and chemical changes. The transport of carbon through this complex environment is crucial to mantle carbon budget but remains the subject of active debate. Synthesis of field studies suggests that carbon subducted with the incoming slab is almost completely returned to the surface environment [Kelemen and Manning, 2015], whereas thermodynamic modelling indicates that a significant portion of carbon is retained in the slab and descends into the deep mantle [Gorman et al., 2006]. To address this controversy and quantify the carbon fluxes within SZs, it is necessary to treat the chemistry of fluid/volatile-rock interaction and the mechanics of porous fluid/volatile migration in a consistent modelling framework. This requirement is met by coupling a thermodynamic parameterization of de/re-volatilization with a two-phase flow model of subduction zones. The two-phase system is assumed to comprise three chemical components: rock containing only non-volatile oxides, H2O and CO2; the fluid phase includes only the latter two. Perple_X is used to map out the binary subsystems rock+H2O and rock+CO2; the results are parameterised in terms of volatile partition coefficients as a function of pressure and temperature. In synthesising the binary subsystems to describe phase equilibria that incorporate all three components, a Margules coefficient is introduced to account for non-ideal mixing of CO2/H2O in the fluid, such that the partition coefficients depend further on bulk composition. This procedure is applied to representative compositions of sediment, MORB, and gabbro for the slab, and peridotite for the mantle. The derived parameterization of each rock type serves as a lightweight thermodynamic module interfaceable with two-phase flow models of SZs. We demonstrate the application of this thermodynamic module through a simple model of carbon flux with a prescribed flow direction through (and out of) the slab. This model allows us to evaluate the effects of flow path and lithology on carbon storage within the slab.
MX Siting Investigation. Geotechnical Evaluation. Detailed Aggregate Resources Study. Pahroc Study Area, Nevada.

DTIC Science & Technology

1981-06-05

source is a fairly limited outcrop of calcareous sandstone classified as dolomite rock (Do). Class RBIb Sources: Pour basin-fill sources within the study...Paleozoic rocks consist of limestone, dolomite , and quartzite with interbedded sandstone and shale. These units are generally exposed along the northern...categories simplify discussion and presentation without altering the conclusions of the study. 2.2.1 Rock Units Dolomite rocks (Do) and carbonate rocks
Quantification of mine-drainage inflows to Little Cottonwood Creek, Utah, using a tracer-injection and synoptic-sampling study

USGS Publications Warehouse

Kimball, B.; Runkel, R.; Gerner, L.

2001-01-01

Historic mining in Little Cottonwood Canyon in Utah has left behind many mine drainage tunnels that discharge water to Little Cottonwood Creek. To quantify the major sources of mine drainage to the stream, synoptic sampling was conducted during a tracer injection under low flow conditions (September 1998). There were distinct increases in discharge downstream from mine drainage and major tributary inflows that represented the total surface and subsurface contributions. The chemistry of stream water determined from synoptic sampling was controlled by the weathering of carbonate rocks and mine drainage inflows. Buffering by carbonate rocks maintained a high pH throughout the study reach. Most of the metal loading was from four surface-water inflows and three subsurface inflows. The main subsurface inflow was from a mine pool in the Wasatch Tunnel. Natural attenuation of all the metals resulted in the formation of colloidal solids, sorption of some metals, and accumulation onto the streambed. The deposition on the streambed could contribute to chronic toxicity for aquatic organisms. Information from the study will help to make decisions about environmental restoration.
The Athena Raman Spectrometer

NASA Technical Reports Server (NTRS)

Wang, Alian; Haskin, Larry A.; Jolliff, Bradley; Wdowiak, Tom; Agresti, David; Lane, Arthur L.

2000-01-01

Raman spectroscopy provides a powerful tool for in situ mineralogy, petrology, and detection of water and carbon. The Athena Raman spectrometer is a microbeam instrument intended for close-up analyses of targets (rock or soils) selected by the Athena Pancam and Mini-TES. It will take 100 Raman spectra along a linear traverse of approximately one centimeter (point-counting procedure) in one to four hours during the Mars' night. From these spectra, the following information about the target will extracted: (1) the identities of major, minor, and trace mineral phases, organic species (e.g., PAH or kerogen-like polymers), reduced inorganic carbon, and water-bearing phases; (2) chemical features (e.g. Mg/Fe ratio) of major minerals; and (3) rock textural features (e.g., mineral clusters, amygdular filling and veins). Part of the Athena payload, the miniaturized Raman spectrometer has been under development in a highly interactive collaboration of a science team at Washington University and the University of Alabama at Birmingham, and an engineering team at the Jet Propulsion Laboratory. The development has completed the brassboard stage and has produced the design for the engineering model.
Geophysical-log and hydraulic-test analyses of groundwater-production wells at the Hannahville Indian Community, Menominee County, Michigan

USGS Publications Warehouse

Bayless, E. Randall; Anderson, J. Alton; Lampe, David C.; Williams, John H.

2013-01-01

The U.S. Geological Survey, in cooperation with the Hannahville Indian Community, evaluated the geohydrology of the bedrock formations and hydraulic properties of groundwater-production wells at the Hannahville Indian Community in Menominee County, Michigan. Geophysical logs were collected from five wells at two sites during September 2012. The logs were analyzed to characterize the lithostratigraphy, bedding and fractures, and hydraulic properties of the geologic formations and aquifers beneath the Hannahville Indian Community. The geophysical logs collected included natural gamma radiation, electromagnetic conductivity, wellbore image, caliper, ambient and stressed flowmeter, fluid resistivity, temperature, and wellbore deviation. The geophysical logs were analyzed with results from short-term hydraulic tests to estimate the transmissivity and water-level altitudes of flow zones penetrated by the wells. The geophysical log analysis indicated the wells penetrated four distinct lithostratigraphic units—shale and carbonate rock, upper carbonate rock, carbonate rock and glauconitic sandstone, and lower carbonate rock. Most of the fractures penetrated by the wellbores appeared to be related bedding partings. The lower carbonate rock unit contained solution features. Analysis of the geophysical logs and hydraulic tests indicated that each of the five wells penetrated from one to four flow zones. The Casino 5 well penetrated a flow zone that was associated with solution features and had an estimated total transmissivity of 4,280 feet squared per day (ft2/d), the highest estimate for all the wells. The Casino 3 well penetrated four flow zones and had an estimated total transmissivity of 3,570 ft2/d. The flow zones penetrated in the lower carbonate rock unit by the Casino 3 and 5 wells were hydraulically connected. The Golf Shack well penetrated two flow zones and had an estimated total transmissivity of 40 ft2/d, the lowest estimate for all the wells. The Community 1 and Community 2 wells penetrated three and four flow zones, respectively, and had estimated total transmissivity values of 185 and 280 ft2/d, respectively.
Rates of CO2 Mineralization in Geological Carbon Storage.

PubMed

Zhang, Shuo; DePaolo, Donald J

2017-09-19

Geologic carbon storage (GCS) involves capture and purification of CO 2 at industrial emission sources, compression into a supercritical state, and subsequent injection into geologic formations. This process reverses the flow of carbon to the atmosphere with the intention of returning the carbon to long-term geologic storage. Models suggest that most of the injected CO 2 will be "trapped" in the subsurface by physical means, but the most risk-free and permanent form of carbon storage is as carbonate minerals (Ca,Mg,Fe)CO 3 . The transformation of CO 2 to carbonate minerals requires supply of the necessary divalent cations by dissolution of silicate minerals. Available data suggest that rates of transformation are highly uncertain and difficult to predict by standard approaches. Here we show that the chemical kinetic observations and experimental results, when they can be reduced to a single cation-release time scale that describes the fractional rate at which cations are released to solution by mineral dissolution, show sufficiently systematic behavior as a function of pH, fluid flow rate, and time that the rates of mineralization can be estimated with reasonable certainty. The rate of mineralization depends on both the abundance (determined by the reservoir rock mineralogy) and the rate at which cations are released from silicate minerals by dissolution into pore fluid that has been acidified with dissolved CO 2 . Laboratory-measured rates and field observations give values spanning 8 to 10 orders of magnitude, but when they are evaluated in the context of a reservoir-scale reactive transport simulation, this range becomes much smaller. The reservoir scale simulations provide limits on the applicable conditions under which silicate mineral dissolution and subsequent carbonate mineral precipitation are likely to occur (pH 4.5 to 6, fluid flow velocity less than 5 m/year, and 50-100 years or more after the start of injection). These constraints lead to estimates of 200 to 2000 years for conversion of 60-90% of injected CO 2 when the reservoir rock has a sufficient volume fraction of divalent cation-bearing silicate minerals and confirms that when reservoir rock mineralogy is not favorable the fraction of CO 2 converted to carbonate minerals is minimal over 10 4 years. A sufficient amount of reactive minerals is typically about 20% by volume. Our approach may allow for rapid evaluation of mineralization potential of subsurface storage reservoirs and illustrates how reservoir scale modeling can be integrated with other observations to address key issues relating to engineering of geologic systems.
Geophysical Signatures to Monitor Fluids and Mineralization for CO2 Sequestration in Basalts

NASA Astrophysics Data System (ADS)

Otheim, L. T.; Adam, L.; Van Wijk, K.; Batzle, M. L.; Mcling, T. L.; Podgorney, R. K.

2011-12-01

Carbon dioxide sequestration in large reservoirs can reduce emissions of this green house gas into the atmosphere. Basalts are promising host rocks due to their volumetric extend, worldwide distribution, and recent observations that CO2-water mixtures react with basalt minerals to precipitate as carbonate minerals, trapping the CO2. The chemical reaction between carbonic acid and minerals rich in calcium, magnesium and iron precipitates carbonates in the pore space. This process would increase the elastic modulus and velocity of the rock. At the same time, the higher compressibility of CO2 over water changes the elastic properties of the rock, decreasing the saturated rock bulk modulus and the P-wave velocity. Reservoirs where the rock properties change as a result of fluid or pressure changes are commonly monitored with seismic methods. Here we present experiments to study the feasibility of monitoring CO2 migration in a reservoir and CO2-rock reactions for a sequestration scenario in basalts. Our goal is to measure the rock's elastic response to mineralization with non-contacting ultrasonic lasers, and the effect of fluid substitution at reservoir conditions at seismic and ultrasonic frequencies. For the fluid substitution experiment we observe changes in the P- and S-wave velocities when saturating the sample with super-critical (sc) CO2, CO2-water mixtures and water alone for different pore and confining pressures. The bulk modulus of the rock is significantly dependent on frequency in the 2~to 106~Hz range, for CO2-water mixtures and pure water saturations. Dry and pure CO2 (sc or gas) do not show a frequency dependence on the modulus. Moreover, the shear wave modulus is not dispersive for either fluid. The frequency dependence of the elastic parameters is related to the attenuation (1/Q) of the rock. We will show the correlation between frequency dependent moduli and attenuation data for the different elastic moduli of the rocks. Three other basalt samples were stored in a pressure chamber with a sc CO2-water solution to study the effect of mineralization on the elastic properties of the rock. The rock elastic properties are recorded with non-contacting ultrasonic lasers at room conditions. After 15 weeks the first post-mineralization scan showed differences in the rock velocities with respect to the pre-mineralization scan. The analysis is done through coda wave interferometry and direct arrivals. The samples were inserted back into the pressure vessel for continuing mineralization and subsequent scans. Finally, we will discuss the applicability of Gassmann's equation and how the combination of mineralization together with CO2-water mixture affects the velocity of waves in basalt rocks.
Carbon Isotopes of Alkanes in Hydrothermal Abiotic Organic Synthesis Processes at High Temperatures and Pressures: An Experimental Study

NASA Technical Reports Server (NTRS)

Fu, Qi; Socki, Richard A.; Niles, Paul B.

2010-01-01

Observation of methane in the Martian atmosphere has been reported by different detection techniques [1-4]. With more evidence showing extensive water-rock interaction in Martian history [5-7], abiotic formation by Fischer-Tropsch Type (FTT) synthesis during serpentization reactions may be one possible process responsible for methane generation on Mars [8, 9]. While the experimental studies performed to date leave little doubt that chemical reactions exist for the abiotic synthesis of organic compounds by mineral surface-catalyzed reactions [10-12], little is known about the reaction pathways by which CO2 and/or CO are reduced under hydrothermal conditions. Carbon and hydrogen isotope measurements of alkanes have been used as an effective tool to constrain the origin and reaction pathways of hydrocarbon formation. Alkanes generated by thermal breakdown of high molecular weight organic compounds have carbon and hydrogen isotopic signatures completely distinct from those formed abiotically [13-15]. Recent experimental studies, however, showed that different abiogenic hydrocarbon formation processes (e.g., polymerization vs. depolymerization) may have different carbon and hydrogen isotopic patterns [16]. Results from previous experiments studying decomposition of higher molecular weight organic compounds (lignite) also suggested that pressure could be a crucial factor affecting fractionation of carbon isotopes [17]. Under high pressure conditions, no experimental data are available describing fractionation of carbon isotope during mineral catalyzed FTT synthesis. Thus, hydrothermal experiments present an excellent opportunity to provide the requisite carbon isotope data. Such data can also be used to identify reaction pathways of abiotic organic synthesis under experimental conditions.
How does the composition affect the mechanical behaviour of simulated clay-rich fault gouges?

NASA Astrophysics Data System (ADS)

Bakker, Elisenda; Spiers, Christopher J.; Hangx, Suzanne J. T.

2014-05-01

CO2 capture and storage (CCS) in depleted oil and gas reservoirs is seen as one of the most promising large-scale CO2-mitigation strategies. Prediction of the effect of fluid-rock interaction on the mechanical integrity and sealing capacity of a reservoir-seal system, on timescales of the order of 1,000 or 10,000 years, is important to ensure the safety and containment of a reservoir in relation to long-term CO2 storage. However, most chemical reactions in rock/CO2/brine systems are slow, which means that long-term effects of fluids on rock composition, microstructure, mechanical properties and transport properties cannot be easily reproduced under laboratory conditions. One way to overcome this problem is to use simulated fault gouges in experiments, investigating a range of possible mineralogical compositions resulting from CO2-exposure. Previous studies have shown that the mechanical and transport properties of clay-rich fault gouges are significantly influenced by the mineralogy, particularly by the presence and relative amount of secondary phases, such as quartz and/or carbonate. In CCS settings, where dissolution and/or precipitation of carbonates may play an important role, the carbonate:clay ratio is expected to influence fault frictional behaviour. This is supported by the different behaviour of phyllosilicates, which generally show stable slip behaviour (aseismic), compared to carbonates, which have shown to become prone to unstable slip (potentially seismic) with increasing temperature. However, little is known about the mechanical and transport properties of carbonate/clay mixtures. We investigated the effect of the carbonate:clay ratio on fault friction, fault reactivation potential and slip stability, i.e. seismic vs. aseismic behaviour, as well as transmissivity evolution during and after fault reactivation. We used two types of starting material, derived from crushed Opalinus Claystone (Mont Terri, Switzerland): i) untreated samples consisting mainly of phyllosilicates (60%), quartz (~20%) and calcite (~15-25%) and ii) "leached" samples consisting of phyllosilicate (65%) and quartz (35%), where the removal of the calcite represents a worst-case scenario for rock/CO2/brine (dissolution) reactions. We performed triaxial direct shear experiments at relevant in-situ temperatures (60-120°C) under saturated conditions (Pp = 25 MPa), using demineralized water as pore fluid, at an effective normal stress (σn) of 50 MPa and shear velocities of 0.22 to 10.9 μm/s. Preliminary results show that the shear strength of the leached samples decreases by ~10-15% with respect to the natural, untreated clay samples. Typical steady-state friction coefficient values obtained for the natural samples are in the range 0.27-0.33, whereas for the leached samples they vary between 0.24 and 0.27. These values are significantly lower than typical friction coefficient values obtained for pure calcite (i.e. 0.62 to 0.71). Both natural and leached samples show velocity strengthening behaviour. The slip stability of the natural gouge appears to be slightly more temperature dependent, showing somewhat higher values of the stability (rate and state friction) parameter (a-b) for lower temperatures.
Early trace of life from 3.95 Ga sedimentary rocks in Labrador, Canada

NASA Astrophysics Data System (ADS)

Tashiro, Takayuki; Ishida, Akizumi; Hori, Masako; Igisu, Motoko; Koike, Mizuho; Méjean, Pauline; Takahata, Naoto; Sano, Yuji; Komiya, Tsuyoshi

2017-09-01

The vestiges of life in Eoarchean rocks have the potential to elucidate the origin of life. However, gathering evidence from many terrains is not always possible, and biogenic graphite has thus far been found only in the 3.7-3.8 Ga (gigayears ago) Isua supracrustal belt. Here we present the total organic carbon contents and carbon isotope values of graphite (δ13Corg) and carbonate (δ13Ccarb) in the oldest metasedimentary rocks from northern Labrador. Some pelitic rocks have low δ13Corg values of -28.2, comparable to the lowest value in younger rocks. The consistency between crystallization temperatures of the graphite and metamorphic temperature of the host rocks establishes that the graphite does not originate from later contamination. A clear correlation between the δ13Corg values and metamorphic grade indicates that variations in the δ13Corg values are due to metamorphism, and that the pre-metamorphic value was lower than the minimum value. We concluded that the large fractionation between the δ13Ccarb and δ13Corg values, up to 25‰, indicates the oldest evidence of organisms greater than 3.95 Ga. The discovery of the biogenic graphite enables geochemical study of the biogenic materials themselves, and will provide insight into early life not only on Earth but also on other planets.
Early trace of life from 3.95 Ga sedimentary rocks in Labrador, Canada.

PubMed

Tashiro, Takayuki; Ishida, Akizumi; Hori, Masako; Igisu, Motoko; Koike, Mizuho; Méjean, Pauline; Takahata, Naoto; Sano, Yuji; Komiya, Tsuyoshi

2017-09-27

The vestiges of life in Eoarchean rocks have the potential to elucidate the origin of life. However, gathering evidence from many terrains is not always possible, and biogenic graphite has thus far been found only in the 3.7-3.8 Ga (gigayears ago) Isua supracrustal belt. Here we present the total organic carbon contents and carbon isotope values of graphite (δ 13 C org ) and carbonate (δ 13 C carb ) in the oldest metasedimentary rocks from northern Labrador. Some pelitic rocks have low δ 13 C org values of -28.2, comparable to the lowest value in younger rocks. The consistency between crystallization temperatures of the graphite and metamorphic temperature of the host rocks establishes that the graphite does not originate from later contamination. A clear correlation between the δ 13 C org values and metamorphic grade indicates that variations in the δ 13 C org values are due to metamorphism, and that the pre-metamorphic value was lower than the minimum value. We concluded that the large fractionation between the δ 13 C carb and δ 13 C org values, up to 25‰, indicates the oldest evidence of organisms greater than 3.95 Ga. The discovery of the biogenic graphite enables geochemical study of the biogenic materials themselves, and will provide insight into early life not only on Earth but also on other planets.
Co-precipitation of dissolved organic matter by calcium carbonate in Pyramid Lake, Nevada

USGS Publications Warehouse

Leenheer, Jerry A.; Reddy, Michael M.

2008-01-01

Our previous research has demonstrated that dissolved organic matter (DOM) influences calcium carbonate mineral formation in surface and ground water. To better understand DOM mediation of carbonate precipitation and DOM co-precipitation and/or incorporation with carbonate minerals, we characterized the content and speciation of DOM in carbonate minerals and in the lake water of Pyramid Lake, Nevada, USA. A 400-gram block of precipitated calcium carbonate from the Pyramid Lake shore was dissolved in 8 liters of 10% acetic acid. Particulate matter not dissolved by acetic acid was removed by centrifugation. DOM from the carbonate rock was fractionated into nine portions using evaporation, dialysis, resin adsorption, and selective precipitations to remove acetic acid and inorganic constituents. The calcium carbonate rock contained 0.23% DOM by weight. This DOM was enriched in polycarboxylic proteinaceous acids and hydroxy-acids in comparison with the present lake water. DOM in lake water was composed of aliphatic, alicyclic polycarboxylic acids. These compound classes were found in previous studies to inhibit calcium carbonate precipitation. DOM fractions from the carbonate rock were 14C-age dated at about 3,100 to 3,500 years before present. The mechanism of DOM co-precipitation and/or physical incorporation in the calcium carbonate is believed to be due to formation of insoluble calcium complexes with polycarboxylic proteinaceous acids and hydroxy-acids that have moderately large stability constants at the alkaline pH of the lake. DOM co-precipitation with calcium carbonate and incorporation in precipitated carbonate minerals removes proteinaceous DOM, but nearly equivalent concentrations of neutral and acidic forms of organic nitrogen in DOM remain in solution. Calcium carbonate precipitation during lime softening pretreatment of drinking water may have practical applications for removal of proteinaceous disinfection by-product precursors.
Prediction of Reservoir Properties for Geomechanical Analysis Using 3-D Seismic Data and Rock Physics Modeling in the Vaca Muerta Formation, Neuquen Basin, Argentina

NASA Astrophysics Data System (ADS)

Convers-Gomez, Carlos E.

The Vaca Muerta Formation in the Neuquen Basin has recently received a lot of attention from oil companies interested in developing its shale resources. Early identification of potential zones with possible good production is extremely important to optimize the return on capital investment. Developing a work flow in shale plays that associates an effective hydraulic fracture response with the presence of hydrocarbons is crucial for economic success. The vertical and lateral heterogeneity of rock properties are critical factors that impact production. The integration of 3D seismic and well data is necessary for prediction of rock properties and identifies their distribution in the rock, which can also be integrated with geomechanical properties to model the rock response favorable to hydraulic stimulation. This study includes a 3D seismic survey and six vertical wells with full log suites in each well. The well logs allowed for the computation of a pre-stack model-based inversion which uses seismic data to estimate rock property volumes. An inverse relationship between P-impedance and Total Organic Content (TOC) was observed and quantified. Likewise, a direct relationship between P-impedance and volume of carbonate was observed. The volume of kerogen, type of clay, type of carbonate and fluid pressure all control the geomechanical properties of the formation when subject to hydraulic fracturing. Probabilistic Neural Networks were then used to predict the lateral and vertical heterogeneity of rock properties. TOC and volume of kerogen behaved as adequate indicators of possible zones with high presence of hydrocarbons. Meanwhile, the volume of carbonate was a valid indicator of brittle-ductile rock. The predicted density volume was used to estimate geomechanical properties (Young's Modulus and Poisson's Ratio) and to identify the zones that have a better response to hydraulic stimulation. During the analysis of geomechanical properties, Young's Modulus was observed to have a direct relationship with volume of carbonate and an inverse relationship with TOC, enabling the identification of brittle and ductile rocks zones. The analysis detected zones that had a good presence of hydrocarbons and brittle rock. The information was integrated with the analysis of geomechanical properties generating a model with the most possible zones of good production. This model will aid in the future exploration and development of the Vaca Muerta Formation.
Melting curve of compressed barium carbonate from in situ ionic conductivity measurements: Implications for the melting behavior of alkaline earth carbonates in Earth's deep carbon cycle

NASA Astrophysics Data System (ADS)

Dong, J.; Li, J.; Zhu, F.; Li, Z.; Farawi, R.

2017-12-01

The whereabouts of subducted carbonates place a major constraint on the Earth's deep carbon cycle, but the fraction of carbon retained in the slab and transported into the deep mantle, compared to that released from the slab and recycled to the surface, is still under debate. Knowledge of the stability of carbonated mantle rocks is pivotal for assessing the ability of slabs to carry carbonates into the deep mantle. Determination and systematic comparison of the melting curves of alkali and alkaline earth carbonates at high pressure can help construct thermodynamic models to predict the melting behavior of complex carbonated mantle rocks. Among alkaline earth carbonates, the melting behavior of barium carbonate (BaCO3) has not been adequately understood. The reported melting point of BaCO3at 1 bar differ by nearly 800 °C and constraints on the melting curve of BaCO3 at high pressure are not available. In this study, the melting temperatures of BaCO3 were determined up to 11 GPa from in situ ionic conductivity measurements using the multi-anvil apparatus at the University of Michigan. The solid-liquid boundary at high pressure was detected on the basis of a steep rise in conductivity through the sample upon melting. The melting point of BaCO3 was found to drop from 1797 °C at 3.3 GPa to 1600 °C at 5.5 GPa and then rise with pressure to 2180 °C at 11 GPa. The observed melting depression point at 5.5 GPa corresponds to the phase transition of BaCO3 from the aragonite structure (Pmcn) to post-aragonite structure (Pmmn) at 6.3 GPa, 877 °C and 8.0 GPa, 727 °C, determined from synchrotron X-ray diffraction measurements using laser-heated DAC experiments at the Advanced Photon Source, Argonne National Laboratory. These results are also compared with ex situ falling marker experiments, and the three methods together place tight constraints on the melting curve of BaCO3 and elucidates the effect of structural phase transitions on its melting behavior.

Numerical Simulation of Electrical Properties of Carbonate Reservoir Rocks Using µCT Images

NASA Astrophysics Data System (ADS)

Colgin, J.; Niu, Q.; Zhang, C.; Zhang, F.

2017-12-01

Digital rock physics involves the modern microscopic imaging of geomaterials, digitalization of the microstructure, and numerical simulation of physical properties of rocks. This physics-based approach can give important insight into understanding properties of reservoir rocks, and help reveal the link between intrinsic rock properties and macroscopic geophysical responses. The focus of this study is the simulation of the complex conductivity of carbonate reservoir rocks using reconstructed 3D rock structures from high-resolution X-ray micro computed tomography (µCT). Carbonate core samples with varying lithofacies and pore structures from the Cambro-Ordovician Arbuckle Group and the Upper Pennsylvanian Lansing-Kansas City Group in Kansas are used in this study. The wide variations in pore geometry and connectivity of these samples were imaged using µCT. A two-phase segmentation method was used to reconstruct a digital rock of solid particles and pores. We then calculate the effective electrical conductivity of the digital rock volume using a pore-scale numerical approach. The complex conductivity of geomaterials is influenced by the electrical properties and geometry of each phase, i.e., the solid and fluid phases. In addition, the electrical double layer that forms between the solid and fluid phases can also affect the effective conductivity of the material. In the numerical modeling, the influence of the electrical double layer is quantified by a complex surface conductance and converted to an apparent volumetric complex conductivity of either solid particles or pore fluid. The effective complex conductivity resulting from numerical simulations based on µCT images will be compared to results from laboratory experiments on equivalent rock samples. The imaging and digital segmentation method, assumptions in the numerical simulation, and trends as compared to laboratory results will be discussed. This study will help us understand how microscale physics affects macroscale electrical conductivity in porous media.
Pimienta-Tamabra(!) - A giant supercharged petroleum system in the southern Gulf of Mexico, onshore and offshore Mexico

USGS Publications Warehouse

Magoon, L.B.; Hudson, T.L.; Cook, H.E.

2001-01-01

Pimienta-Tamabra(!) is a giant supercharged petroleum system in the southern Gulf of Mexico with cumulative production and total reserves of 66.3 billion barrels of oil and 103.7 tcf of natural gas, or 83.6 billion barrels of oil equivalent (BOE). The effectiveness of this system results largely from the widespread distribution of good to excellent thermally mature, Upper Jurassic source rock underlying numerous stratigraphic and structural traps that contain excellent carbonate reservoirs. Expulsion of oil and gas as a supercritical fluid from Upper Jurassic source rock occurred when the thickness of overburden rock exceeded 5 km. This burial event started in the Eocene, culminated in the Miocene, and continues to a lesser extent today. The expelled hydrocarbons started migrating laterally and then upward as a gas-saturated 35-40??API oil with less than 1 wt.% sulfur and a gas-to-oil ratio (GOR) of 500-1000 ft3/BO. The generation-accumulation efficiency is about 6%.
The carbonatite-marble dykes of Abyan Province, Yemen Republic: the mixing of mantle and crustal carbonate materials revealed by isotope and trace element analysis

NASA Astrophysics Data System (ADS)

Le Bas, M. J.; Ba-Bttat, M. A. O.; Taylor, R. N.; Milton, J. A.; Windley, B. F.; Evins, P. M.

2004-09-01

Dykes of carbonate rocks, that cut gneisses in the Lowder-Mudiah area of southern Yemen, consist of dolomite and/or calcite with or without apatite, barite and monazite. Petrographic observations, mineralogical, XRF and ICP-MS analyses reveal that some of the carbonate rocks are derived from sedimentary protoliths, whereas others are magmatic calcio- and magnesio-carbonatites some of which are mineralized with barite-monazite. The interbanded occurrence and apparent contemporary emplacement of these different rock types within individual dykes, backed by Sr Nd isotope evidence, are interpreted to show that intrusion of mantle-derived carbonatite magma was accompanied by mobilization of crustal marbles. That took place some 840 Ma ago but the REE-mineralization is dated at ca. 400 Ma.
Characterization of LIBS emission lines for the identification of chlorides, carbonates, and sulfates in salt/basalt mixtures for the application to MSL ChemCam data: LIBS OF CL, C, S IN SALT-BASALT MIXTURES

DOE Office of Scientific and Technical Information (OSTI.GOV)

Anderson, D. E.; Ehlmann, B. L.; Forni, O.

Ancient environmental conditions on Mars can be probed through the identification of minerals on its surface, including water-deposited salts and cements dispersed in the pore space of sedimentary rocks. Laser-induced breakdown spectroscopy (LIBS) analyses by the Martian rover Curiosity's ChemCam instrument can indicate salts, and ChemCam surveys aid in identifying and selecting sites for further, detailed in situ analyses. Here, we performed laboratory LIBS experiments under simulated Mars conditions with a ChemCam-like instrument on a series of mixtures containing increasing concentrations of salt in a basaltic background to investigate the potential for identifying and quantifying chloride, carbonate, and sulfate saltsmore » found only in small amounts, dispersed in bulk rock with ChemCam, rather than concentrated in veins. The data then indicate that the presence of emission lines from the basalt matrix limited the number of Cl, C, and S emission lines found to be useful for quantitative analysis; nevertheless, several lines with intensities sensitive to salt concentration were identified. Detection limits for the elements based on individual emission lines ranged from ~20 wt % carbonate (2 wt % C), ~5–30 wt % sulfate (1–8 wt % S), and ~5–10 wt % chloride (3–6 wt % Cl) depending on the basaltic matrix and/or salt cation. Absolute quantification of Cl, C, and S in the samples via univariate analysis depends on the cation-anion pairing in the salt but appears relatively independent of matrices tested, following normalization. Our results are promising for tracking relative changes in the salt content of bulk rock on the Martian surface with ChemCam.« less
Characterization of LIBS emission lines for the identification of chlorides, carbonates, and sulfates in salt/basalt mixtures for the application to MSL ChemCam data: LIBS OF CL, C, S IN SALT-BASALT MIXTURES

DOE PAGES

Anderson, D. E.; Ehlmann, B. L.; Forni, O.; ...

2017-04-24

Ancient environmental conditions on Mars can be probed through the identification of minerals on its surface, including water-deposited salts and cements dispersed in the pore space of sedimentary rocks. Laser-induced breakdown spectroscopy (LIBS) analyses by the Martian rover Curiosity's ChemCam instrument can indicate salts, and ChemCam surveys aid in identifying and selecting sites for further, detailed in situ analyses. Here, we performed laboratory LIBS experiments under simulated Mars conditions with a ChemCam-like instrument on a series of mixtures containing increasing concentrations of salt in a basaltic background to investigate the potential for identifying and quantifying chloride, carbonate, and sulfate saltsmore » found only in small amounts, dispersed in bulk rock with ChemCam, rather than concentrated in veins. The data then indicate that the presence of emission lines from the basalt matrix limited the number of Cl, C, and S emission lines found to be useful for quantitative analysis; nevertheless, several lines with intensities sensitive to salt concentration were identified. Detection limits for the elements based on individual emission lines ranged from ~20 wt % carbonate (2 wt % C), ~5–30 wt % sulfate (1–8 wt % S), and ~5–10 wt % chloride (3–6 wt % Cl) depending on the basaltic matrix and/or salt cation. Absolute quantification of Cl, C, and S in the samples via univariate analysis depends on the cation-anion pairing in the salt but appears relatively independent of matrices tested, following normalization. Our results are promising for tracking relative changes in the salt content of bulk rock on the Martian surface with ChemCam.« less
Intra-slab COH fluid fluxes evidenced by fluid-mediated decarbonation of lawsonite eclogite-facies altered oceanic metabasalts

NASA Astrophysics Data System (ADS)

Vitale Brovarone, Alberto; Chu, Xu; Martin, Laure; Ague, Jay J.; Monié, Patrick; Groppo, Chiara; Martinez, Isabelle; Chaduteau, Carine

2018-04-01

The interplay between the processes controlling the mobility of H2O and C-bearing species during subduction zone metamorphism exerts a critical control on plate tectonics and global volatile recycling. Here we present the first study on fresh, carbonate-bearing, lawsonite eclogite-facies metabasalts from Alpine Corsica, France, which reached the critical depths at which important devolatilization reactions occur in subducting slabs. The studied samples indicate that the evolution of oceanic crustal sequences subducted under present-day thermal regimes is dominated by localized fluid-rock interactions that are strongly controlled by the nature and extent of inherited (sub)seafloor hydrothermal processes, and by the possibility of deep fluids to be channelized along inherited or newly-formed discontinuities. Fluid channelization along inherited discontinuities controlled local rehydration and dehydration/decarbonation reactions and the stability of carbonate and silicate minerals at the blueschist-eclogite transition. Fluid-mediated decarbonation was driven by upward, up-temperature fluid flow in the inverted geothermal gradient of a subducting oceanic slab, a process that has not been documented in natural samples to date. We estimate that the observed fluid-rock reactions released 20-60 kg CO2 per m3 of rock (i.e. 0.7-2.1 wt% CO2), which is in line with the values predicted from decarbonation of metabasalts in open systems at these depths. Conversely, the estimated time-integrated fluid fluxes (20-50 t/m2) indicate that the amount of carbon transported by channelized fluid flow within the volcanic part of subducting oceanic plates is potentially much higher than previous numerical estimates, testifying to the percolation of C-bearing fluids resulting from devolatilization/dissolution processes operative in large reservoirs.
The sedimentary organic matter from a Lake Ichkeul core (far northern Tunisia): Rock-Eval and biomarker approach

NASA Astrophysics Data System (ADS)

Affouri, Hassène; Sahraoui, Olfa

2017-05-01

The vertical distributions of bulk and molecular biomarker composition in samples from a ca. 156 cm sediment core from Lake Ichkeul were determined. Bulk analysis (Rock-Eval pyrolysis, carbonate, lipid extraction) and molecular analysis of saturated fractions were used to characterize the nature, preservation conditions and input of sedimentary organic matter (OM) to this sub-wet lake environment. The sediments are represented mainly by gray-black silty-clay facies where the carbonate (CaCO3) content varies in a range of 10-30% dry sediment. Rock-Eval pyrolysis revealed a homogeneous total organic carbon (TOC) content of ca. 1% sediment, but with down core fluctuation, indicating different anoxic conditions at different depths and material source variation. The values show three periods of relative enrichment, exceeding ca. 1%, at 146-134 cm, 82 cm and 14-0 cm depth. The low Hydrogen Index (HI) values [<119 mg hydrocarbon (HC)/g TOC)] were characteristic of continental Type III OM. The Tmax values in the range 415-420 °C were characteristic of immature OM at an early diagenetic stage. The distributions of n-alkanes (C17 to C34), isoprenoid (iso) alkanes (pristane and phytane), terpanes and steranes showed that the OM is a mixture of marine algal and bacterial source and emergent and floating higher plant origin. In addition, the distributions, as well as several biomarker ratios (n-alkanes, iso-alkanes/n-alkanes), showed that the OM is a mixture of immature and mature. Significant downcore fluctuation was observed in the molecular composition. This indicates intense microbial activity below ca. 50 cm core depth under an anoxic and brackish environment.
Lithologic mapping in the Mountain Pass, California area using Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) data

USGS Publications Warehouse

Rowan, L.C.; Mars, J.C.

2003-01-01

Evaluation of an Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) image of the Mountain Pass, California area indicates that several important lithologic groups can be mapped in areas with good exposure by using spectral-matching techniques. The three visible and six near-infrared bands, which have 15-m and 30-m resolution, respectively, were calibrated by using in situ measurements of spectral reflectance. Calcitic rocks were distinguished from dolomitic rocks by using matched-filter processing in which image spectra were used as references for selected spectral categories. Skarn deposits and associated bright coarse marble were mapped in contact metamorphic zones related to intrusion of Mesozoic and Tertiary granodioritic rocks. Fe-muscovite, which is common in these intrusive rocks, was distinguished from Al-muscovite present in granitic gneisses and Mesozoic granite. Quartzose rocks were readily discriminated, and carbonate rocks were mapped as a single broad unit through analysis of the 90-m resolution, five-band surface emissivity data, which is produced as a standard product at the EROS Data Center. Three additional classes resulting from spectral-angle mapper processing ranged from (1) a broad granitic rock class (2) to predominately granodioritic rocks and (3) a more mafic class consisting mainly of mafic gneiss, amphibolite and variable mixtures of carbonate rocks and silicate rocks. ?? 2002 Elsevier Science Inc. All rights reserved.
Zebra textures in carbonate rocks: Fractures produced by the force of crystallization during mineral replacement

NASA Astrophysics Data System (ADS)

Wallace, Malcolm W.; Hood, Ashleigh v. S.

2018-06-01

Zebra textures are enigmatic banded fabrics that occur in many carbonate-hosted ore deposits, dolomite hydrocarbon reservoirs and carbonate successions globally. They consist of a variety of minerals and are characterised by parallel light and dark bands that occur at a millimetre- to centimetre-scale. Based on petrological evidence, there is general consensus that the dark bands formed by replacement of the carbonate host rock. Historically, more contention surrounds the origin of the light bands, but the dominant view is that these are mineral-filled cavities, which is supported by overwhelming textural evidence. Overall, the feature common to all versions of zebra textures is mineral replacement of the original carbonate host. We suggest that mineral replacement (and the force of crystallization) in association with open space generation is a viable mechanism for the development of zebra cavity systems. Dissolution and open space generation in either evaporites or carbonates adjacent to the site of replacement reactions is necessary to remove the confining pressure from the rock and to allow the development of fractures. The pressure of the growing replacement crystals within the carbonate pervasively splits the carbonate apart, producing thin strips of carbonate surrounded by open space. The fractures may then be subject to dissolution and are later filled by cements. Very regular stratabound zebra textures (as found in ore deposits like Cadjebut, Australia and San Vicente, Peru) may be related to stratabound dissolution (of evaporites or carbonates), whereas irregularly distributed zebra textures are more likely to be associated with irregular carbonate dissolution.
Confocal Imaging of porous media

NASA Astrophysics Data System (ADS)

Shah, S.; Crawshaw, D.; Boek, D.

2012-12-01

Carbonate rocks, which hold approximately 50% of the world's oil and gas reserves, have a very complicated and heterogeneous structure in comparison with sandstone reservoir rock. We present advances with different techniques to image, reconstruct, and characterize statistically the micro-geometry of carbonate pores. The main goal here is to develop a technique to obtain two dimensional and three dimensional images using Confocal Laser Scanning Microscopy. CLSM is used in epi-fluorescent imaging mode, allowing for the very high optical resolution of features well below 1μm size. Images of pore structures were captured using CLSM imaging where spaces in the carbonate samples were impregnated with a fluorescent, dyed epoxy-resin, and scanned in the x-y plane by a laser probe. We discuss the sample preparation in detail for Confocal Imaging to obtain sub-micron resolution images of heterogeneous carbonate rocks. We also discuss the technical and practical aspects of this imaging technique, including its advantages and limitation. We present several examples of this application, including studying pore geometry in carbonates, characterizing sub-resolution porosity in two dimensional images. We then describe approaches to extract statistical information about porosity using image processing and spatial correlation function. We have managed to obtain very low depth information in z -axis (~ 50μm) to develop three dimensional images of carbonate rocks with the current capabilities and limitation of CLSM technique. Hence, we have planned a novel technique to obtain higher depth information to obtain high three dimensional images with sub-micron resolution possible in the lateral and axial planes.
Carbonate-silicate liquid immiscibility upon impact melting, Ries Crater, Germany

NASA Astrophysics Data System (ADS)

Graup, Guenther

1999-05-01

The 24-km-diameter Ries impact crater in southern Germany is one of the most studied impact structures on Earth. The Ries impactor struck a Triassic to Upper Jurassic sedimentary sequence overlying Hercynian crystalline basement. At the time of impact (14.87 +/- 0.36 Ma; Storzer et al., 1995), the 350 m thick Malm limestone was present only to the S and E of the impact site. To the N and W, the Malm had been eroded away, exposing the underlying Dogger and Lias. The largest proportion of shocked target material is in the impact melt-bearing breccia suevite. The suevite had been believed to be derived entirely from the crystalline basement. Calcite in the suevite has been interpreted as a post-impact hydrothermal deposit. From optical inspection of 540 thin sections of suevite from 32 sites, I find that calcite in the suevite shows textural evidence of liquid immiscibility with the silicate impact melt. Textural evidence of liquid immiscibility between silicate and carbonate melt in the Ries suevite includes: carbonate globules within silicate glass, silicate globules embedded in carbonate, deformable and coalescing carbonate spheres within silicate glass, sharp menisci or cusps and budding between silicate and carbonate melt, fluidal textures and gas vesicles in carbonate schlieren, a quench crystallization sequence of the carbonate, spinifex textured quenched carbonate, separate carbonate spherules in the suevite mineral-fragment-matrix, and inclusions of mineral fragments suspended in carbonate blebs. Given this evidence of liquid immiscibility, the carbonate in the suevite has, therefore, like the silicate melt a primary origin by impact shock melting. Evidence of carbonate-silicate liquid immiscibility is abundant in the suevites to the SW to E of the Ries crater. The rarer suevites to the W to NE of the crater are nearly devoid of carbonate melts. This correspondence between the occurrence of outcropping limestones at the target surface and the formation of carbonate melt, indicates that the Malm limestones are the source rocks of the carbonate impact melt. This correspondence shows that the suevites preserve a compositional memory of their source rocks. From the regional distribution of suevites with or without immiscible carbonate melts, it is inferred that the Ries impactor hit the steep Albtrauf escarpment at its toe, in an oblique impact from the north.
Mineral storage of CO2/H2S gas mixture injection in basaltic rocks

NASA Astrophysics Data System (ADS)

Clark, D. E.; Gunnarsson, I.; Aradottir, E. S.; Oelkers, E. H.; Sigfússon, B.; Snæbjörnsdottír, S. Ó.; Matter, J. M.; Stute, M.; Júlíusson, B. M.; Gíslason, S. R.

2017-12-01

Carbon capture and storage is one solution to reducing CO2 emissions in the atmosphere. The long-term geological storage of buoyant supercritical CO2 requires high integrity cap rock. Some of the risk associated with CO2 buoyancy can be overcome by dissolving CO2 into water during its injection, thus eliminating its buoyancy. This enables injection into fractured rocks, such as basaltic rocks along oceanic ridges and on continents. Basaltic rocks are rich in divalent cations, Ca2+, Mg2+ and Fe2+, which react with CO2 dissolved in water to form stable carbonate minerals. This possibility has been successfully tested as a part of the CarbFix CO2storage pilot project at the Hellisheiði geothermal power plant in Iceland, where they have shown mineralization occurs in less than two years [1, 2]. Reykjavik Energy and the CarbFix group has been injecting a mixture of CO2 and H2S at 750 m depth and 240-250°C since June 2014; by 1 January 2016, 6290 tons of CO2 and 3530 tons of H2S had been injected. Once in the geothermal reservoir, the heat exchange and sufficient dissolution of the host rock neutralizes the gas-charged water and saturates the formation water respecting carbonate and sulfur minerals. A thermally stable inert tracer was also mixed into the stream to monitor the subsurface transport and to assess the degree of subsurface carbonation and sulfide precipitation [3]. Water and gas samples have been continuously collected from three monitoring wells and geochemically analyzed. Based on the results, mineral saturation stages have been defined. These results and tracer mass balance calculations are used to evaluate the rate and magnitude of CO2 and H2S mineralization in the subsurface, with indications that mineralization of carbon and sulfur occurs within months. [1] Gunnsarsson, I., et al. (2017). Rapid and cost-effective capture and subsurface mineral storage of carbon and sulfur. Manuscript submitted for publication. [2] Matter, J., et al. (2016). Rapid carbon mineralization for permanent disposal of anthropogenic carbon dioxide emissions. Science 352 (6291), 1312-1314. [3] Snæbjörnsdottír, S.O., et al. (2017). The chemistry and saturation states of subsurface fluids during the in-situ mineralisation of CO2 and H2S at the CarbFix site in SW-Iceland. International Journal of Greenhouse Gas Control 58, 87-102.
Characterization of rock samples and mineralogical controls on leachates

USGS Publications Warehouse

Hammarstrom, Jane M.; Cravotta, Charles A.; Galeone, Daniel G.; Jackson, John C.; Dulong, Frank T.; Hornberger, Roger J.; Brady, Keith B.C.

2009-01-01

Rocks associated with coal beds typically include shale, sandstone, and (or) limestone. In addition to common rock-forming minerals, all of these rock types may contain sulfide and sulfate minerals, various carbonate minerals, and organic material. These different minerals have inherently different solubility characteristics, as well as different acid-generating or acid-neutralizing potentials. The abundance and composition of sulfur- and carbonate-bearing minerals are of particular interest in interpreting the leaching column data because (1) pyrite and carbonate minerals are the primary controls on the acid-base account of a sample, (2) these minerals incorporate trace metals that can be released during weathering, and (3) these minerals readily react during weathering due to mineral dissolution and oxidation of iron.Rock samples were collected by the Pennsylvania Department of Environmental Protection (PaDEP) from five different sites to assess the draft standardized leaching column method (ADTI-WP2) for the prediction of weathering rates and water quality at coal mines. Samples were sent to USGS laboratories for mineralogical characterization and to ActLabs for chemical analysis. The samples represent a variety of rock types (shales, sandstones, and coal refuse) that are typical of coal overburden in the eastern United States. These particular samples were chosen for testing the weathering protocols because they represent a range of geochemical and lithologic characteristics, sulfur contents, and acid-base accounting characteristics (Hornberger et al., 2003). The rocks contain variable amounts of pyrite and carbonate minerals and vary in texture.This chapter includes bulk rock chemical data and detailed mineralogical and textural data for unweathered starting materials used in the interlaboratory validation study, and for two samples used in the early phases of leaching column tests (Wadesville Sandstone, Leechburg Coal Refuse). We also characterize some of the post-weathering rock samples, report trace-element content in leachate, and discuss mineralogical controls on leachate quality based on data from one of the participating laboratories. Table 5.1 lists the samples described in this chapter, the sample numbers, and comments on the characteristics of each lithology. Sample locations are plotted in Figure 5.1. Chapters 2 and 3 describe the sample locations, sample preparation protocols, ABA characteristics, and rationale for selection of rock samples for testing. Microprobe data for pyrite and carbonate minerals are tabulated in Appendix 5.1. Leachate data, along with a series of graphs showing concentration and cumulative transport trends, for the laboratory data discussed in this chapter are included as Excel spreadsheets in Appendices 5.2 and 5.3. Leach column data for the interlaboratory study are evaluated and interpreted in Chapters 7 -11.
Conceptual model of the Great Basin carbonate and alluvial aquifer system

USGS Publications Warehouse

Heilweil, Victor M.; Brooks, Lynette E.

2011-01-01

A conceptual model of the Great Basin carbonate and alluvial aquifer system (GBCAAS) was developed by the U.S. Geological Survey (USGS) for a regional assessment of groundwater availability as part of a national water census. The study area is an expansion of a previous USGS Regional Aquifer Systems Analysis (RASA) study conducted during the 1980s and 1990s of the carbonate-rock province of the Great Basin. The geographic extent of the study area is 110,000 mi2, predominantly in eastern Nevada and western Utah, and includes 165 hydrographic areas (HAs) and 17 regional groundwater flow systems.A three-dimensional hydrogeologic framework was constructed that defines the physical geometry and rock types through which groundwater moves. The diverse sedimentary units of the GBCAAS study area are grouped into hydrogeologic units (HGUs) that are inferred to have reasonably distinct hydrologic properties due to their physical characteristics. These HGUs are commonly disrupted by large-magnitude offset thrust, strike-slip, and normal faults, and locally affected by caldera formation. The most permeable aquifer materials within the study area include Cenozoic unconsolidated sediments and volcanic rocks, along with Mesozoic and Paleozoic carbonate rocks. The framework was built by extracting and combining information from digital elevation models, geologic maps, cross sections, drill hole logs, existing hydrogeologic frameworks, and geophysical data.
Geochemical, isotopic and geochronological characterization of listvenite from the Upper Unit on Tinos, Cyclades, Greece

NASA Astrophysics Data System (ADS)

Hinsken, Tim; Bröcker, Michael; Strauss, Harald; Bulle, Florian

2017-06-01

We describe a largely unknown listvenite deposit from Tinos, Cyclades, Greece and combine field observations with petrographic, bulk-rock geochemical, isotope (Sr, O, C), and Rb-Sr geochronological data. The volumetrically small listvenite occurrences are associated with metabasic phyllites, talc schists, meta-gabbros, ophicalcites and serpentinites of the Upper Unit. Geochemical characteristics (high Mg#, Cr, Ni), as well as preserved relic Cr-spinel and the typical mesh-texture of serpentinized Mg-silicates, document derivation from ultramafic precursors. Judging from field and textural observations it is very likely that carbonation affected serpentinite and not unaltered meta-peridotite. The direct contact or transition zones to ultramafic rocks are not preserved, but serpentinites that escaped carbonation are closely associated. The listvenites occur near a low-angle normal fault that probably focused fluid infiltration and distribution. The carbonation is associated with the influx of CO2-rich, K-bearing fluids that led to the formation of ferroan magnesite, quartz and Cr-bearing white mica (fuchsite), but otherwise the transformation of serpentinized peridotite into listvenite had been a largely isochemical process. The studied rocks do not contain elevated concentrations of precious metals (Au, Pt, Pd). Field relationships suggest that the listvenite-bearing occurrences most likely represent the same tectonostratigraphic level as Upper Unit rocks that had been thermally overprinted in the contact aureole of Miocene granitoids at ca. 15 Ma. Accordingly the intrusion depth provides a minimum pressure constraint for the somewhat older carbonation. Pressure estimates for thermally overprinted rocks and the granitoids suggest an intrusion depth of ca. 7-10 km that corresponds to a pressure of ca. 2-3 kbar. Chlorite thermometry applied to the Tinos listvenites mostly indicates temperatures of ca. 250 °C during carbonation. Internal Rb-Sr mineral isochrons (different grain-size fractions of fuchsite and magnesite) yielded apparent ages of ca. 16 Ma and ca. 19 Ma, respectively, which are interpreted to date carbonation and associated fuchsite formation. The new ages indicate that listvenite formation is considerably younger than the presumed Late Cretaceous or Jurassic protolith age of the ultramafic precursors and also post-dates tectonic juxtaposition of the Upper Unit onto the Lower Unit at ca. 21 Ma. Although not the dominant process, a contribution of contact metamorphic decarbonation cannot completely be ruled out. The Sr isotope characteristics of magnesite and whole rocks correspond very well to the seawater curve for the formation age indicated by Rb-Sr dating. Carbonate carbon and oxygen isotopes measured for the listvenites suggest that magnesite formed following the deep circulation of fluids and their interaction with other carbonate rocks (possibly the marble units present on Tinos) including a possible contribution from magmatic CO2. The similarity in δ13C and δ18O between listvenite and some of the ophicalcite occurrences could indicate a common origin from the same circulating fluids, but remains elusive at present. Combined, P-T constraints and Sr isotope data imply infiltration of seawater-dominated fluids to a depth of several kilometers. This conclusion is supported by oxygen and carbon isotope data.
Geo-Mechanical Characterization of Carbonate Rock Masses by Means of Laser Scanner Technique

NASA Astrophysics Data System (ADS)

Palma, Biagio; Parise, Mario; Ruocco, Anna

2017-12-01

Knowledge of the geometrical and structural setting of rock masses is crucial to evaluate the stability and to design the most suitable stabilization works. In this work we use the Terrestrial Laser Scanning (TLS) at the site of the Grave of the Castellana Caves, a famous show cave in southern Italy. The Grave is the natural access to the cave system, produced by collapse of the vault, due to upward progression of instabilities in the carbonate rock masses. It is about 55-m high, bell-shaped, with maximum width of 120 m. Aim of the work is the characterization of carbonate rock masses from the structural and geo-mechanical standpoints through the use of innovative survey techniques. TLS survey provides a product consisting of millions of geo-referenced points, to be managed in space, to become a suitable database for the morphological and geological-structural analysis. Studying by means of TLS a rock face, partly inaccessible or located in very complex environments, allows to investigate slopes in their overall areal extent, thus offering advantages both as regards safety of the workers and time needed for the survey. In addition to TLS, the traditional approach was also followed by performing scanlines surveys along the rims of the Grave, following the ISRM recommendations for characterization of discontinuity in rock masses. A quantitative comparison among the data obtained by TLS technique and those deriving from the classical geo-mechanical survey is eventually presented, to discuss potentiality of drawbacks of the different techniques used for surveying the rock masses.
Adsorption of Anionic, Cationic and Nonionic Surfactants on Carbonate Rock in Presence of ZrO 2 Nanoparticles

NASA Astrophysics Data System (ADS)

Esmaeilzadeh, Pouriya; Bahramian, Alireza; Fakhroueian, Zahra

The adsorption of surfactants at the solid-water interface is important for the control of wetting, lubrication, detergency and in mineral flotation.We have studied the adsorptions of different types of surfactants, cationic (Dodecyl trimethylammonium bromide, DTAB), anionic (sodium dodecyl sulfate, SDS) and non-anionic (lauryl alcohol-7 mole ethoxylate, LA7) on carbonate rock in presence of zirconium oxide spherical nanoparticles (17-19 nm). ZrO2 nanoparticles with tetrahedral structure have significant effect on adsorption of surfactants on the carbonate rock. We have used the measured conductivities to determine the rate of adsorption of surfactants at rock-water interfaces. The conductivity of DTAB in aqueous solutions containing calcite powder decreases more than the other surfactants in contact with ZrO2 nanoparticles. We have also investigated the adsorption of surfactants at the air-water interface. The presence of nanoparticles, as demonstrated by our experiments, enhances the surface activity and surface adsorption of the surfactants through electrostatic forces or formation of nanostructures. Dynamic light structuring data shows similar aggregation number of nanoparticles in presence of nanoparticles.
Determination of chlorine in silicate rocks

USGS Publications Warehouse

Peck, L.C.

1959-01-01

In a rapid accurate method for the determination of chlorine in silicate rocks, the rock powder is sintered with a sodium carbonate flux containing zinc oxide and magnesium carbonate. The sinter cake is leached with water, the resulting solution is filtered, and the filtrate is acidified with nitric acid. Chlorine is determined by titrating this solution with mercuric nitrate solution using sodium nitroprusside as the indicator. The titration is made in the dark with a beam of light shining through the solution. The end point of the titration is found by visually comparing the intensity of this beam of light with that of a similar beam of light in a reference solution.
Monitoring the hydrothermal system in Long Valley caldera, California

USGS Publications Warehouse

Farrar, C.D.; Sorey, M.L.

1985-01-01

An ongoing program to monitor the hydrothermal system in Long Valley for changes caused by volcanic or tectonic processes has produced considerable data on the water chemistry and discharge of springs and fluid temperatures and pressures in wells. Chemical and isotopic data collected under this program have greatly expanded the knowledge of chemical variability both in space and time. Although no chemical or isotopic changes in hot spring waters can be attributed directly to volcanic or tectonic processes, changes in hot spring chemistry that have been recorded probably relate to interactions between and variations in the quantity of liquid and gas discharged. Stable carbon isotope data are consistent with a carbon source either perform the mantle or from metamorphosed carbonate rocks. Continuous and periodic measurements of hot spring discharge at several sites show significant co seismic and a seismic changes since 1980.
The influence of seawater carbonate chemistry, mineralogy, and diagenesis on calcium isotope variations in Lower-Middle Triassic carbonate rocks

DOE PAGES

Lau, Kimberly V.; Maher, Kate; Brown, Shaun T.; ...

2017-11-01

The geological calcium cycle is linked to the geological carbon cycle through the weathering and burial of carbonate rocks. As a result, calcium (Ca) isotope ratios ( 44 Ca/ 40 Ca, expressed as δ 44/40 Ca) can help to constrain ancient carbon cycle dynamics if Ca cycle behavior can be reconstructed. But, the δ 44/40 Ca of carbonate rocks is influenced not only by the δ 44/40 Ca of seawater but also by diagenetic processes and fractionation associated with carbonate precipitation. In this study, we investigate the dominant controls on carbonate δ 44/40 Ca in Upper Permian to Middle Triassicmore » limestones (ca. 253 to 244 Ma) from south China and Turkey. This time interval is ideal for assessing controls on Ca isotope ratios in carbonate rocks because fluctuations in seawater δ 44/40 Ca may be expected based on several large carbon isotope (δ 13 C) excursions ranging from -2 to + 8‰. Parallel negative δ 13 C and δ 44/40 Ca excursions were previously identified across the end-Permian extinction horizon. Here, we find a second negative excursion in δ 44/40 Ca of ~ 0.2‰ within Lower Triassic strata in both south China and Turkey; however, this excursion is not synchronous between regions and thus cannot be interpreted to reflect secular change in the δ 44/40 Ca of global seawater. Additionally, δ 44/40 Ca values from Turkey are consistently 0.3‰ lower than contemporaneous samples from south China, providing further support for local or regional influences. By measuring δ 44/40 Ca and Sr concentrations ([Sr]) in two stratigraphic sections located at opposite margins of the Paleo-Tethys Ocean, we can determine whether the data represent global conditions (e.g., secular variations in the δ 44/40 Ca of seawater) versus local controls (e.g., original mineralogy or diagenetic alteration). The [Sr] and δ 44/40 Ca data from this study are best described statistically by a log-linear correlation that also exists in many previously published datasets of various geological ages. By using a model of early marine diagenetic water-rock interaction, we illustrate that this general correlation can be explained by the chemical evolution of bulk carbonate sediment samples with different initial mineralogical compositions that subsequently underwent recrystallization. Although early diagenetic resetting and carbonate mineralogy strongly influence the carbonate δ 44/40 Ca values, the relationship between [Sr] and δ 44/40 Ca holds potential for reconstructing first-order secular changes in seawater δ 44/40 Ca composition.« less

The influence of seawater carbonate chemistry, mineralogy, and diagenesis on calcium isotope variations in Lower-Middle Triassic carbonate rocks

DOE Office of Scientific and Technical Information (OSTI.GOV)

Lau, Kimberly V.; Maher, Kate; Brown, Shaun T.

The geological calcium cycle is linked to the geological carbon cycle through the weathering and burial of carbonate rocks. As a result, calcium (Ca) isotope ratios ( 44 Ca/ 40 Ca, expressed as δ 44/40 Ca) can help to constrain ancient carbon cycle dynamics if Ca cycle behavior can be reconstructed. But, the δ 44/40 Ca of carbonate rocks is influenced not only by the δ 44/40 Ca of seawater but also by diagenetic processes and fractionation associated with carbonate precipitation. In this study, we investigate the dominant controls on carbonate δ 44/40 Ca in Upper Permian to Middle Triassicmore » limestones (ca. 253 to 244 Ma) from south China and Turkey. This time interval is ideal for assessing controls on Ca isotope ratios in carbonate rocks because fluctuations in seawater δ 44/40 Ca may be expected based on several large carbon isotope (δ 13 C) excursions ranging from -2 to + 8‰. Parallel negative δ 13 C and δ 44/40 Ca excursions were previously identified across the end-Permian extinction horizon. Here, we find a second negative excursion in δ 44/40 Ca of ~ 0.2‰ within Lower Triassic strata in both south China and Turkey; however, this excursion is not synchronous between regions and thus cannot be interpreted to reflect secular change in the δ 44/40 Ca of global seawater. Additionally, δ 44/40 Ca values from Turkey are consistently 0.3‰ lower than contemporaneous samples from south China, providing further support for local or regional influences. By measuring δ 44/40 Ca and Sr concentrations ([Sr]) in two stratigraphic sections located at opposite margins of the Paleo-Tethys Ocean, we can determine whether the data represent global conditions (e.g., secular variations in the δ 44/40 Ca of seawater) versus local controls (e.g., original mineralogy or diagenetic alteration). The [Sr] and δ 44/40 Ca data from this study are best described statistically by a log-linear correlation that also exists in many previously published datasets of various geological ages. By using a model of early marine diagenetic water-rock interaction, we illustrate that this general correlation can be explained by the chemical evolution of bulk carbonate sediment samples with different initial mineralogical compositions that subsequently underwent recrystallization. Although early diagenetic resetting and carbonate mineralogy strongly influence the carbonate δ 44/40 Ca values, the relationship between [Sr] and δ 44/40 Ca holds potential for reconstructing first-order secular changes in seawater δ 44/40 Ca composition.« less
Tracing Life in the Earliest Terrestrial Rock Record

NASA Astrophysics Data System (ADS)

Lepland, A.; van Zuilen, M.; Arrhenius, G.

2001-12-01

The principal method for studying the earliest traces of life in the metamorphosed, oldest (> 3.5 Ga) terrestrial rocks involves determination of isotopic composition of carbon, mainly prevailing as graphite. It is generally believed that this measure can distinguish biogenic graphite from abiogenic varieties. However, the interpretation of life from carbon isotope ratios has to be assessed within the context of specific geologic circumstances requiring (i) reliable protolith interpretation (ii) control of secondary, metasomatic processes, and (iii) understanding of different graphite producing mechanisms and related carbon isotopic systematics. We have carried out a systematic study of abundance, isotopic composition and petrographic associations of graphite in rocks from the ca. 3.8 Ga Isua Supracrustal Belt (ISB) in southern West Greenland. Our study indicates that most of the graphite in ISB occurs in carbonate-rich metasomatic rocks (metacarbonates) while sedimentary units, including banded iron formations (BIFs) and metacherts, have exceedingly low graphite concentrations. Regardless of isotopic composition of graphite in metacarbonate rocks, their secondary origin disqualifies them from providing evidence for traces of life stemming from 3.8 Ga. Recognition of the secondary origin of Isua metacarbonates thus calls for reevaluation of biologic interpretations by Schidlowski et al. (1979) and Mojzsis et al. (1996) that suggested the occurrence of 3.8 Ga biogenic graphite in these rocks. The origin of minute quantities of reduced carbon, released from sedimentary BIFs and metacherts at combustion steps > 700 C remains to be clarified. Its isotopic composition (d13C from -18 to -25%) may hint at a biogenic origin. However, such isotopically light carbon was also found in Proterozoic mafic dykes cross-cutting the metasedimentary units in the ISB. The occurrence of isotopically light, reduced carbon in biologically irrelevant dykes may indicate secondary graphite crystallization from CO2 or CH4- containing fluids that in turn may derive from bioorganic sources. If this were the case, trace amounts of isotopically light secondary graphite can also be expected in metasediments, complicating the usage of light graphite as primary biomarker. The possibility of recent organic contamination, particularly important in low graphite samples, needs also to be considered; it appears as a ubiquitous component released at combustion in the 400 to 500 deg range. - A potential use of the apatite-graphite association as a biomarker has been proposed in the study by Mojzsis et al. (1996). Close inspection of several hundred apatite crystals from Isua BIFs and metacherts did, however, not show an association between these two minerals, moreover graphite is practically absent in these metasediments. In contrast, apatite crystals in the non-sedimentary metacarbonate rocks were found commonly to have invaginations, coatings and inclusions of abundant graphite. Considering that such graphite inclusions in apatite are restricted to the secondary metasomatic carbonate rocks in the ISB this association can not be considered as a primary biomarker in the Isua Supracrustal Belt References: Mojzsis,S.J, .Arrhenius,G., McKeegan, K.D.,.Harrison, T.M.,.Nutman, A.P & C.R.L.Friend.,1996. Nature 384: 55 Schidlowski, M., Appel, P.W.U., Eichmann, R. & Junge, C.E., 1979. Geochim. Cosmochim. Acta 43: 189-190.
Effect of carbonation on leachability, strength and microstructural characteristics of KMP binder stabilized Zn and Pb contaminated soils.

PubMed

Du, Yan-Jun; Wei, Ming-Li; Reddy, Krishna R; Wu, Hao-liang

2016-02-01

This study presents a systematic investigation of effects of carbonation on the contaminant leachability and unconfined compressive strength of KMP stabilized contaminated soils. A field soil spiked with Zn and Pb individually and together is stabilized using a new KMP additive under standard curing conditions and also with carbonation. The KMP additive is composed of oxalic acid-activated phosphate rock, monopotassium phosphate and reactive magnesia. The stabilized soils are tested for acid neutralization capacity, toxic characteristics leaching characteristics, contaminant speciation and unconfined compression strength. X-ray diffraction, scanning electron microscope and energy dispersive spectroscopy analyses are performed to assess reaction products. The results demonstrate that carbonation increases both acid buffer capacity index and unconfined compressive strength, but decreases leachability of KMP stabilized soils. These results are interpreted based on the changes in chemical speciation of Zn and Pb and also stability and solubility of the reaction products (metal phosphates and carbonates) formed in the soils. Overall, this study demonstrates that carbonation has positive effects on leachability and strength of the KMP stabilized soils. Copyright © 2015 Elsevier Ltd. All rights reserved.
Seawater as the source of minor elements in black shales, phosphorites and other sedimentary rocks

USGS Publications Warehouse

Piper, D.Z.

1994-01-01

Many of the minor elements in seawater today have a concentration-depth profile similar to that of the biologically essential nutrients, NO-3 and PO3-4. They show a relative depletion in the photic zone and enrichment in the deep ocean. The difference between their surface- and deep-ocean values, normalized to the change in PO3-4, approaches the average of measured minor-element: P ratios in marine plankton, although individual analyses of the latter show extreme scatter for a variety of reasons. Despite this scatter in the minor-element analyses of plankton, agreement between the two sets of data shows unequivocally that an important marine flux of many minor elements through the ocean is in the form of biogenic matter, with a composition approaching that of plankton. This interpretation is further supported by sediment studies, particularly of sediments which accumulate in shelf-slope environments where biological productivity in the photic zone is exceptionally high and organic carbon contents of the underlying sediment elevated. The interelement relations observed for some of these sediments approach the average values of plankton. These same interelement relations are observed in many marine sedimentary rocks such as metalliferous black shales and phosphorites, rocks which have a high content of marine fractions (e.g., organic matter, apatite, biogenic silica and carbonates). Many previous studies of the geochemistry of these rocks have concluded that local hydrothermal activity, and/or seawater with an elemental content different from that of the modern ocean, was required to account for their minor-element contents. However, the similarity in several of the minor-element ratios in many of these formations to minor-element ratios in modern plankton demonstrates that these sedimentary rocks accumulated in environments whose marine chemistry was virtually identical to that seen on continental shelf-slopes, or in marginal seas, of the ocean today. The accumulation of the marine fraction of minor elements on these ancient sea floors was determined largely by the accumulation of organic matter, settling from the photic zone and with a composition of average plankton. A second marine fraction of minor elements in these rocks accumulated through precipitation and adsorption from seawater. The suite of elements in this fraction reflects redox conditions in the bottom water, as determined by bacterial respiration. For example, high Mn, high Cr+V and high Mo concentrations, above those which can be attributed to the accumulation of planktonic matter, characterize accumulation under bottom-water oxidizing, denitrifying and sulfate-reducing conditions, respectively. ?? 1994.
Authigenic K-feldspar in salt rock (Haselgebirge Formation, Eastern Alps)

NASA Astrophysics Data System (ADS)

Leitner, Christoph

2015-04-01

The crystallisation of authigenic quartz under low temperature, saline conditions is well known (Grimm, 1962). Also the growth of low temperature authigenic feldspar in sediments is a long known phenomenon (Kastner & Siever, 1979; Sandler et al., 2004). In this study we intend to show that halite (NaCl) is a major catalyser for authigenic mineral growth. During late Permian (c. 255-250 Ma), when the later Eastern Alps were located around north of the equator, the evaporites of the Haselgebirge Formation were deposited (Piller et al., 2004). The Haselgebirge Fm. consists in salt mines of a two-component tectonite of c. 50 % halite and 50 % sedimentary clastic and other evaporite rocks (Spötl 1998). Most of the clastic rocks are mud- to siltstones ("mudrock"). During this study, we investigated rare sandstones embedded in salt rock form four Alpine salt mines. Around 40 polished thin sections were prepared by dry grinding for thin section analysis and scanning electron microscopy. The sandstones consist mainly of quartz, K-feldspar, rock fragments, micas, accessory minerals and halite in the pore space. They are fine grained and well sorted. Mudrock clasts in sandstone were observed locally, and also coal was observed repeatedly. Asymmetric ripples were found only in the dimension of millimeters to centimeters. Euhedral halite crystals in pores indicate an early presence of halite. During early diagenesis, authigenic minerals crystallized in the following chronological order. (1) Where carbonate (mainly magnesite) occurred, it first filled the pore space. Plant remains were impregnated with carbonate. (2) Halite precipitated between the detritic sandstone grains. Carbonate grains can be completely embedded in halite. (3) K-feldspar and quartz grains usually expose a detritic core and a later grown euhedral inclusion free rim. Euhedral rims of K-feldspar often also enclose a halite core. K-feldspar replaced the pre-existing halite along former grain boundaries of halite. Fluid reaction rims with many tiny minerals (hematite, acicular crystals, fluid inclusions etc.) around quartz, K-feldspar and rock fragments probably belong to this stage. (4) Authigenic anhydrite grew over carbonate, halite (halite inclusions in anhydrite), euhedral quartz and euhedral K-feldspar. (5). The sulfate polyhalite [K2Ca2Mg(SO4)4•2H2O] needs three major cation ingredients: potassium, calcium and magnesium. The large granoblastic polyhalite crystals enclose halite, euhedral quartz and euhedral K-feldspar. It formed coevally with the authigenic anhydrite, which proves by their intermediate intergrowth. The age of granoblastic polyhalite was measured between 235-210 Ma on samples from the salt mines of Altaussee, Berchtesgaden and Bad Dürrnberg with 39Ar/40Ar dating (Leitner et al., 2014). Since deposition of the Haselgebirge Fm. was at c. 250 Ma, the primary diagenetic crystallization was completed c. 15-30 Ma after deposition. The overburden at this time was 1000-2000 m at maximum (formation of the large carbonate platforms; Tollmann, 1985) and therefore very low p-T conditions can be assumed for the formation of authigenic quartz and authigenic K-feldspar.
Critical elements in sediment-hosted deposits (clastic-dominated Zn-Pb-Ag, Mississippi Valley-type Zn-Pb, sedimentary rock-hosted Stratiform Cu, and carbonate-hosted Polymetallic Deposits): A review: Chapter 12

USGS Publications Warehouse

Marsh, Erin; Hitzman, Murray W.; Leach, David L.

2016-01-01

Some sediment-hosted base metal deposits, specifically the clastic-dominated (CD) Zn-Pb deposits, carbonate-hosted Mississippi Valley-type (MVT) deposits, sedimentary-rock hosted stratiform copper deposits, and carbonate-hosted polymetallic (“Kipushi type”) deposits, are or have been important sources of critical elements including Co, Ga, Ge, and Re. The generally poor data concerning trace element concentrations in these types of sediment-hosted ores suggest that there may be economically important concentrations of critical elements yet to be recognized.
Publications - GMC 284 | Alaska Division of Geological & Geophysical

Science.gov Websites

DGGS GMC 284 Publication Details Title: TOC/rock-eval pyrolysis geochemical data for 26 Alaska North for more information. Bibliographic Reference Unknown, 1999, TOC/rock-eval pyrolysis geochemical data Information gmc284.pdf (1.8 M) Keywords Pyrolysis; Rock-Eval Pyrolysis; Total Organic Carbon Top of Page
Element mobilization and redistribution under extreme tropical weathering of basalts from the Hainan Island, South China

NASA Astrophysics Data System (ADS)

Jiang, Ke; Qi, Hua-Wen; Hu, Rui-Zhong

2018-06-01

Chemical weathering of rocks has substantial influence on the global geochemical cycle. In this paper, the geochemical profile of a well-developed basalt weathering profile (>15 m thick, including soil, saprolite, semi-weathered rock and fresh basalt) on the Island of Hainan (South China) was presented. The soil and saprolite samples from this profile are characterized by high Al2O3 and Fe2O3 concentrations (up to 32.3% and 28.5%, respectively). The mineral assemblage is dominated by kaolinite, Fe-oxides/-hydroxides and gibbsite (or boehmite), indicating extensive desilicate and ferrallitic weathering. The acidic and organic-rich environment in the soil horizon may have promoted elemental remobilization and leaching. The strongest SiO2 depletion and Al2O3 enrichment at about 2.4 m deep indicate that the main kaolinite hydrolysis and gibbsite formation occurred near the soil-saprolite interface. The mild Sr reconcentration at about 3.9 m and 7.1 m deep may be attributed to secondary carbonate precipitation. Mn-oxides/-hydroxides precipitated at 6.1 m deep, accompanied by the strongest enrichment of Ba and Co. Uranium is mildly enriched in the middle part (about 7.1 m and 9.1 m deep) of the weathering profile, and the enrichment may have been caused by the decomposition of uranyl carbonates or the accumulation of zircon. Immobile element (i.e., Zr, Hf, Nb, Ta, Th and Ti) distributions at different depths are mainly controlled by secondary Fe-oxides/-hydroxides, and follow the stability sequence of Nb ≈ Ta ≈ Th > Zr ≈ Hf > Ti. The limited thickness (∼15 cm) of the semi-weathered basalt horizon at the rock-regolith interface (15.28 m deep) suggests that plagioclase and pyroxene are readily altered to kaolinite, smectite and Fe-oxides under tropical climate. The marked enrichment of transitional metals (such as Cu, Zn, Ni, and Sc) along the rock-regolith interface may have associated mainly with increasing pH values, as well as the dissolution of primary apatite and formation of secondary phosphates. Our findings highlight the importance of secondary phosphates in the redistribution of transition metals, and in the possible Mg, Cu, and Ni isotopic fractionation under extreme weathering of basalt in tropic climate.
A model for diurnal patterns of carbon fixation in a Precambrian microbial mat based on a modern analog

NASA Technical Reports Server (NTRS)

Rothschild, L. J.

1991-01-01

Microbial mat communities are one of the first and most prevalent biological communities known from the Precambrian fossil record. These fossil mat communities are found as laminated sedimentary rock structures called stromatolites. Using a modern microbial mat as an analog for Precambrian stromatolites, a study of carbon fixation during a diurnal cycle under ambient conditions was undertaken. The rate of carbon fixation depends primarily on the availability of light (consistent with photosynthetic carbon fixation) and inorganic carbon, and not nitrogen or phosphorus. Atmospheric PCO2 is thought to have decreased from 10 bars at 4 Ga (10(9) years before present) to approximately 10(-4) bars today, implying a change in the availability of inorganic carbon for carbon fixation. Experimental manipulation of levels of inorganic carbon to levels that may have been available to Precambrian mat communities resulted in increased levels of carbon fixation during daylight hours. Combining these data with models of daylength during the Precambrian, models are derived for diurnal patterns of photosynthetic carbon fixation in a Precambrian microbial mat community. The models suggest that, even in the face of shorter daylengths during the Precambrian, total daily carbon fixation has been declining over geological time, with most of the decrease having occurred during the Precambrian.
Geochemistry of groundwater in the Beaver and Camas Creek drainage basins, eastern Idaho

USGS Publications Warehouse

Rattray, Gordon W.; Ginsbach, Michael L.

2014-01-01

The U.S. Geological Survey (USGS), in cooperation with the U.S. Department of Energy, is studying the fate and transport of waste solutes in the eastern Snake River Plain (ESRP) aquifer at the Idaho National Laboratory (INL) in eastern Idaho. This effort requires an understanding of the natural and anthropogenic geochemistry of groundwater at the INL and of the important physical and chemical processes controlling the geochemistry. In this study, the USGS applied geochemical modeling to investigate the geochemistry of groundwater in the Beaver and Camas Creek drainage basins, which provide groundwater recharge to the ESRP aquifer underlying the northeastern part of the INL. Data used in this study include petrology and mineralogy from 2 sediment and 3 rock samples, and water-quality analyses from 4 surface-water and 18 groundwater samples. The mineralogy of the sediment and rock samples was analyzed with X-ray diffraction, and the mineralogy and petrology of the rock samples were examined in thin sections. The water samples were analyzed for field parameters, major ions, silica, nutrients, dissolved organic carbon, trace elements, tritium, and the stable isotope ratios of hydrogen, oxygen, carbon, sulfur, and nitrogen. Groundwater geochemistry was influenced by reactions with rocks of the geologic terranes—carbonate rocks, rhyolite, basalt, evaporite deposits, and sediment comprised of all of these rocks. Agricultural practices near and south of Dubois and application of road anti-icing liquids on U.S. Interstate Highway 15 were likely sources of nitrate, chloride, calcium, and magnesium to groundwater. Groundwater geochemistry was successfully modeled in the alluvial aquifer in Camas Meadows and the ESRP fractured basalt aquifer using the geochemical modeling code PHREEQC. The primary geochemical processes appear to be precipitation or dissolution of calcite and dissolution of silicate minerals. Dissolution of evaporite minerals, associated with Pleistocene Lake Terreton, is an important contributor of solutes in the Mud Lake-Dubois area. Oxidation-reduction reactions are important influences on the chemistry of groundwater at Camas Meadows and the Camas National Wildlife Refuge. In addition, mixing of different groundwaters or surface water with groundwater appears to be an important physical process influencing groundwater geochemistry in much of the study area, and evaporation may be an important physical process influencing the groundwater geochemistry of the Camas National Wildlife Refuge. The mass-balance modeling results from this study provide an explanation of the natural geochemistry of groundwater in the ESRP aquifer northeast of the INL, and thus provide a starting point for evaluating the natural and anthropogenic geochemistry of groundwater at the INL.
Lower Cody Shale (Niobrara equivalent) in the Bighorn Basin, Wyoming and Montana: thickness, distribution, and source rock potential

USGS Publications Warehouse

Finn, Thomas M.

2014-01-01

The lower shaly member of the Cody Shale in the Bighorn Basin, Wyoming and Montana is Coniacian to Santonian in age and is equivalent to the upper part of the Carlile Shale and basal part of the Niobrara Formation in the Powder River Basin to the east. The lower Cody ranges in thickness from 700 to 1,200 feet and underlies much of the central part of the basin. It is composed of gray to black shale, calcareous shale, bentonite, and minor amounts of siltstone and sandstone. Sixty-six samples, collected from well cuttings, from the lower Cody Shale were analyzed using Rock-Eval and total organic carbon analysis to determine the source rock potential. Total organic carbon content averages 2.28 weight percent for the Carlile equivalent interval and reaches a maximum of nearly 5 weight percent. The Niobrara equivalent interval averages about 1.5 weight percent and reaches a maximum of over 3 weight percent, indicating that both intervals are good to excellent source rocks. S2 values from pyrolysis analysis also indicate that both intervals have a good to excellent source rock potential. Plots of hydrogen index versus oxygen index, hydrogen index versus Tmax, and S2/S3 ratios indicate that organic matter contains both Type II and Type III kerogen capable of generating oil and gas. Maps showing the distribution of kerogen types and organic richness for the lower shaly member of the Cody Shale show that it is more organic-rich and more oil-prone in the eastern and southeastern parts of the basin. Thermal maturity based on vitrinite reflectance (Ro) ranges from 0.60–0.80 percent Ro around the margins of the basin, increasing to greater than 2.0 percent Ro in the deepest part of the basin, indicates that the lower Cody is mature to overmature with respect to hydrocarbon generation.
Elements of Eoarchean life trapped in mineral inclusions.

PubMed

Hassenkam, T; Andersson, M P; Dalby, K N; Mackenzie, D M A; Rosing, M T

2017-08-03

Metasedimentary rocks from Isua, West Greenland (over 3,700 million years old) contain 13 C-depleted carbonaceous compounds, with isotopic ratios that are compatible with a biogenic origin. Metamorphic garnet crystals in these rocks contain trails of carbonaceous inclusions that are contiguous with carbon-rich sedimentary beds in the host rock, where carbon is fully graphitized. Previous studies have not been able to document other elements of life (mainly hydrogen, oxygen, nitrogen and phosphorus) structurally bound to this carbonaceous material. Here we study carbonaceous inclusions armoured within garnet porphyroblasts, by in situ infrared absorption on approximately 10 -21 m 3 domains within these inclusions. We show that the absorption spectra are consistent with carbon bonded to nitrogen and oxygen, and probably also to phosphate. The levels of C-H or O-H bonds were found to be low. These results are consistent with biogenic organic material isolated for billions of years and thermally matured at temperatures of around 500 °C. They therefore provide spatial characterization for potentially the oldest biogenic carbon relics in Earth's geological record. The preservation of Eoarchean organic residues within sedimentary material corroborates earlier claims for the biogenic origins of carbon in Isua metasediments.
SUGARLOAF ROADLESS AREA, CALIFORNIA.

USGS Publications Warehouse

Powell, Robert E.; Campbell, Harry W.

1984-01-01

On the basis of geologic, geochemical, and geophysical investigations and a survey of mines, quarries, and prospects the Sugarloaf Roadless Area, California, has little promise for the occurrence of metallic mineral or energy resources. Units of carbonate rock and graphitic schist have demonstrated resources of magnesian marble and graphite. Sand, gravel, and construction stone other than carbonate rock are present in the roadless area, but similar or better quality materials are abundant and more accessible outside the area.
Dissolution-Assisted Pattern Formation During Olivine Carbonation

NASA Astrophysics Data System (ADS)

Lisabeth, Harrison; Zhu, Wenlu; Xing, Tiange; De Andrade, Vincent

2017-10-01

Olivine and pyroxene-bearing rocks in the oceanic crust react with hydrothermal fluids producing changes in the physical characteristics and behaviors of the altered rocks. Notably, these reactions tend to increase solid volume, reducing pore volume, permeability, and available reactive surface area, yet entirely hydrated and/or carbonated rocks are commonly observed in the field. We investigate the evolution of porosity and permeability of fractured dunites reacted with CO2-rich solutions in laboratory experiments. The alteration of crack surfaces changes the mechanical and transport properties of the bulk samples. Analysis of three-dimensional microstructural data shows that although precipitation of secondary minerals causes the total porosity of the sample to decrease, an interconnected network of porosity is maintained through channelized dissolution and coupled carbonate precipitation. The observed microstructure appears to be the result of chemo-mechanical coupling, which may provide a mechanism of porosity maintenance without the need to invoke reaction-driven cracking.
Dissolution-Assisted Pattern Formation During Olivine Carbonation

DOE PAGES

Lisabeth, Harrison; Zhu, Wenlu; Xing, Tiange; ...

2017-08-31

Olivine and pyroxene bearing rocks in the oceanic crust react with hydrothermal fluids producing changes in the physical characteristics and behaviors of the altered rocks. Notably, these reactions tend to increase solid volume, reducing pore volume, permeability and available reactive surface area; yet, entirely hydrated and/or carbonated rocks are commonly observed in the field. We investigate the evolution of porosity and permeability of fractured dunites reacted with CO 2-rich solutions in laboratory experiments. The alteration of crack surfaces changes the mechanical and transport properties of the bulk samples. Analysis of three-dimensional microstructural data shows that although precipitation of secondary mineralsmore » causes the total porosity of the sample to decrease, an interconnected network of porosity is maintained through channelized dissolution and coupled carbonate precipitation. Lastly, the observed microstructure appears to be the result of chemo-mechanical coupling, which may provide a mechanism of porosity maintenance without the need to invoke reaction-driven cracking.« less
Subduction-Zone Metamorphic Pathway for Deep Carbon Cycling: Evidence from the Italian Alps and the Tianshan

NASA Astrophysics Data System (ADS)

Bebout, G. E.; Collins, N.; Cook-Kollars, J.; Angiboust, S.; Agard, P.; Scambelluri, M.; John, T.; Kump, L. R.

2013-12-01

Depending on the magnitude of the poorly constrained C flux in ultramafic rocks, on a global basis, sediments and altered oceanic crust (AOC) together deliver 70-95% of the C currently entering subduction zones. We are investigating extents of retention and metamorphic release of C in deeply subducted AOC and carbonate-rich sediment represented by HP/UHP meta-ophiolitic and metasedimentary rocks in the Italian Alps and in the Tianshan. Study of metapelite devolatilization in the same W. Alps suite (Bebout et al., 2013, Chem. Geol.) provides a geochemical framework for study of C behavior along prograde P-T paths similar to those experienced in forearcs of most modern subduction margins. Study of veins in the Tianshan affords examination of C mobility in UHP fluids, in later stages as metabasaltic rocks were fragmented in the subduction channel. Our results for sediments and AOC indicate impressive retention of oxidized C (carbonate) and reduced C (variably metamorphosed organic matter) to depths approaching those beneath arc volcanic fronts. In metasedimentary rocks, extensive isotopic exchange between the oxidized and reduced C resulted in shifts in both reservoirs toward upper mantle compositions. Much of the carbonate in metabasalts has C and O isotopic compositions overlapping with those for carbonate in AOC, with some HP/UHP metamorphic veins showing greater influence of organic C signatures from metasedimentary rocks. Calculations of prograde devolatilization histories using Perple-X demonstrate that, in most forearcs, very little decarbonation occurs in the more carbonate-rich rocks unless they are flushed by H2O-rich fluids from an external source, for example, from the hydrated ultramafic section of subducting slabs (cf. Gorman et al., 2006; G3) or from more nearby rocks experiencing dehydration (e.g., metapelites). A comparison of the most recently published thermal models for modern subduction zones (van Keken et al., 2011, JGR) with calculated and experimentally determined phase relations indicates that significant C loss during devolatilization (and partial melting) should occur as subducting sections traverse depths beneath arcs. The extent of C mobility due to carbonate dissolution remains uncertain. On a global basis, imbalance between subducted C input and C return flux by magmatism (excluding ultramafic inputs, ~40×20% of subducted C return via arcs and ~80×20% by all magmatism; Bebout, 2013, Treat. Geochem.) indicates net modern C return to the mantle, perhaps a reversal of Archean net outgassing (despite more rapid subduction). Global C cycle models predict that relatively small (and geologically plausible) change in the subduction/volcanic C flux could significantly affect atmospheric CO2 levels and thus global climate.
On nutrients and trace metals: Effects from Enhanced Weathering

NASA Astrophysics Data System (ADS)

Amann, T.; Hartmann, J.

2015-12-01

The application of rock flour on suitable land ("Enhanced Weathering") is one proposed strategy to reduce the increase of atmospheric CO2 concentrations. At the same time it is an old and established method to add fertiliser and influence soil properties. Investigations of this method focused on the impact on the carbonate system, as well as on engineering aspects of a large-scale application, but potential side effects were never discussed quantitatively. We analysed about 120,000 geochemically characterised volcanic rock samples from the literature. Applying basic statistics, theoretical release rates of nutrients and potential contaminants by Enhanced Weathering were evaluated for typical rock types. Applied rock material can contain significant amounts of essential or beneficial nutrients (potassium, phosphorus, micronutrients). Their release can partly cover the demand of major crops like wheat, rice or corn, thereby increasing crop yield on degraded soils. However, the concentrations of considered elements are variable within a specific rock type, depending on the geological setting. High heavy metal concentrations are found in (ultra-) basic rocks, the class with the highest CO2 drawdown potential. More acidic rocks contain less or no critical amounts, but sequester less CO2. Findings show that the rock selection determines the capability to supply significant amounts of nutrients, which could partly substitute industrial mineral fertiliser usage. At the same time, the release of harmful trace element has to be considered. Through careful selection of regionally available rocks, benefits could be maximised and drawbacks reduced. The deployment of Enhanced Weathering to sequester CO2 and to ameliorate soils necessitates an ecosystem management, considering the release and fate of weathered elements in plants, soils and water. Cropland with degraded soils would benefit while having a net negative CO2 effect, while other carbon dioxide removal strategies, like afforestation, biofuel production, and biochar application could benefit from Enhanced Weathering side effects, as organic carbon pools are positively influenced.
The thin section rock physics: Modeling and measurement of seismic wave velocity on the slice of carbonates

NASA Astrophysics Data System (ADS)

Wardaya, P. D.; Noh, K. A. B. M.; Yusoff, W. I. B. W.; Ridha, S.; Nurhandoko, B. E. B.

2014-09-01

This paper discusses a new approach for investigating the seismic wave velocity of rock, specifically carbonates, as affected by their pore structures. While the conventional routine of seismic velocity measurement highly depends on the extensive laboratory experiment, the proposed approach utilizes the digital rock physics view which lies on the numerical experiment. Thus, instead of using core sample, we use the thin section image of carbonate rock to measure the effective seismic wave velocity when travelling on it. In the numerical experiment, thin section images act as the medium on which wave propagation will be simulated. For the modeling, an advanced technique based on artificial neural network was employed for building the velocity and density profile, replacing image's RGB pixel value with the seismic velocity and density of each rock constituent. Then, ultrasonic wave was simulated to propagate in the thin section image by using finite difference time domain method, based on assumption of an acoustic-isotropic medium. Effective velocities were drawn from the recorded signal and being compared to the velocity modeling from Wyllie time average model and Kuster-Toksoz rock physics model. To perform the modeling, image analysis routines were undertaken for quantifying the pore aspect ratio that is assumed to represent the rocks pore structure. In addition, porosity and mineral fraction required for velocity modeling were also quantified by using integrated neural network and image analysis technique. It was found that the Kuster-Toksoz gives the closer prediction to the measured velocity as compared to the Wyllie time average model. We also conclude that Wyllie time average that does not incorporate the pore structure parameter deviates significantly for samples having more than 40% porosity. Utilizing this approach we found a good agreement between numerical experiment and theoretically derived rock physics model for estimating the effective seismic wave velocity of rock.
A four-dimensional petroleum systems model for the San Joaquin Basin Province, California: Chapter 12 in Petroleum systems and geologic assessment of oil and gas in the San Joaquin Basin Province, California

USGS Publications Warehouse

Peters, Kenneth E.; Magoon, Leslie B.; Lampe, Carolyn; Scheirer, Allegra Hosford; Lillis, Paul G.; Gautier, Donald L.

2008-01-01

A calibrated numerical model depicts the geometry and three-dimensional (3-D) evolution of petroleum systems through time (4-D) in a 249 x 309 km (155 x 192 mi) area covering all of the San Joaquin Basin Province of California. Model input includes 3-D structural and stratigraphic data for key horizons and maps of unit thickness, lithology, paleobathymetry, heat flow, original total organic carbon, and original Rock-Eval pyrolysis hydrogen index for each source rock. The four principal petroleum source rocks in the basin are the Miocene Antelope shale of Graham and Williams (1985; hereafter referred to as Antelope shale), the Eocene Kreyenhagen Formation, the Eocene Tumey formation of Atwill (1935; hereafter referred to as Tumey formation), and the Cretaceous to Paleocene Moreno Formation. Due to limited Rock-Eval/total organic carbon data, the Tumey formation was modeled using constant values of original total organic carbon and original hydrogen index. Maps of original total organic carbon and original hydrogen index were created for the other three source rocks. The Antelope shale was modeled using Type IIS kerogen kinetics, whereas Type II kinetics were used for the other source rocks. Four-dimensional modeling and geologic field evidence indicate that maximum burial of the three principal Cenozoic source rocks occurred in latest Pliocene to Holocene time. For example, a 1-D extraction of burial history from the 4-D model in the Tejon depocenter shows that the bottom of the Antelope shale source rock began expulsion (10 percent transformation ratio) about 4.6 Ma and reached peak expulsion (50 percent transformation ratio) about 3.6 Ma. Except on the west flank of the basin, where steep dips in outcrop and seismic data indicate substantial uplift, little or no section has been eroded. Most petroleum migration occurred during late Cenozoic time in distinct stratigraphic intervals along east-west pathways from pods of active petroleum source rock in the Tejon and Buttonwillow depocenters to updip sandstone reservoirs. Satisfactory runs of the model required about 18 hours of computation time for each simulation using parallel processing on a Linux-based cluster.
A case study on the application of isotope ratio mass spectrometry (IRMS) in determining the provenance of a rock used in an alleged nickel switching incident.

PubMed

Roelofse, F; Horstmann, U E

2008-01-15

The application of isotope ratio mass spectrometry (IRMS) in forensic science to establish the provenance of a range of questioned substances including soils, drugs, explosives, currency, ivory and rhino horn has been widely documented. The present study wishes to highlight the applicability of IRMS and specifically stable carbon IRMS in determining the provenance of a carbonate rock that was switched for nickel metal exported from South Africa to Israel. The technique employed effectively argued against a South African origin for the rock whilst simultaneously supporting an Israeli origin, enabling investigators to focus their attention accordingly. The study represents the first documented instance known to the authors where IRMS has been employed in the forensic geo-location of a rock.

Sediments and fossiliferous rocks from the eastern side of the Tongue of the Ocean, Bahamas

USGS Publications Warehouse

Gibson, T.G.; Schlee, J.

1967-01-01

In August 1966, two dives were made with the deep-diving submersible Alvin along the eastern side of the Tongue of the Ocean to sample the rock and sediment. Physiographically, the area is marked by steep slopes of silty carbonate sediment and precipitous rock cliffs dusted by carbonate debris. Three rocks, obtained from the lower and middle side of the canyon (914-1676 m depth), are late Miocene-early Pliocene to late Pleistocene-Recent in age; all are deep-water pelagic limestones. They show (i) that the Tongue of the Ocean has been a deep-water area at least back into the Miocene, and (ii) that much shallow-water detritus has been swept off neighbouring banks to be incorporated with the deep-water fauna in the sediment. ?? 1967 Pergamon Press Ltd.
Synthesis of fluorine- doped silica-coating by fluorosilane nanofluid to ultrahydrophobic and ultraoleophobic surface

NASA Astrophysics Data System (ADS)

Saboori, R.; Azin, R.; Osfouri, Sh; Sabbaghi, S.; Bahramian, A.

2017-10-01

Liquid repellency treatment has many applications in various sectors including oil and gas reservoirs and self-cleaning surfaces. In this study, effect of silica, fluorine-doped silica and fluorine-doped silica-coating by fluorosilane nanofluid on ultrahydrophobic and ultraoleophobic surface of carbonate and sandstone rock were investigated. The nanoparticles were synthesized by sol-gel method and characterized using XRD, FTIR, FESEM and DLS and nanofluid was prepared. F-SiO2-F nanoparticle was adsorbed on surface of rocks and confirmed by FESEM and EDXA. Effect of nanofluid on wettability was investigated by measuring contact angles of water, crude oil, condensate, n-decane and ethylene glycol in air and stability of ultrahydrophobic and ultraoleophobic was investigated. Results show that nanofluid (0.05 wt% of nanoparticle) changes contact angle from strongly liquid-wet to strongly gas-wet in all systems. The original contact angle of water, crude oil, condensate, n-decane and ethylene glycol were 37.95°, 0°, 0°, 0° and 0° for carbonate rock and 40.30°, 0°, 0°, 0° and 0° for sandstone rock which altered to 146.47°, 145.59°, 138.24°, 139.06° and 146.52° for carbonate rock and 160.01°, 151.40°, 131.85°, 140.27° and 151.70° for sandstone rock after treatment. The ultraoleophobic and ultrahydrophobic stability were >48 h and 120 min.
Potential for formation of disinfection by-products from storage of chlorinated surface water in the Basalt aquifer near Fallon, Nevada

USGS Publications Warehouse

Fram, Miranda S.; Maurer, Douglas K.; Lico, Michael S.

2005-01-01

Increased pumpage from a basalt aquifer near Fallon, Nevada, has caused its water levels to decline and has induced changes in the quality of water pumped from the basalt. The aquifer is the sole source of water for municipal supply to the city of Fallon, the Naval Air Station Fallon, and the Fallon Paiute-Shoshone Tribe. These changes may be mitigated by storage of surface water in the basalt for subsequent use. Because chlorination of the surface water may be required for storage, the U.S. Geological Survey, in cooperation with the Fallon Paiute-Shoshone Tribe, made laboratory tests using laboratory carbon-organic-free water, surface-water, ground-water, and basaltic-rock samples to determine the potential for formation of disinfection by-products. Experiments with water samples only (no rock and no chlorine) indicated no change in dissolved-organic-carbon (DOC) concentrations over a 20-day reaction period; whereas, all experiments using rock, water, and no chlorine indicated an increase in DOC concentrations. The greatest increase in DOC concentrations for all three water samples occurred in experiments with the rock samples from outcrops on Rattlesnake Hill. Experiments with water only and chlorine yielded a total trihalomethane (THM) concentration of 97.4 ?g/L for the ground-water sample and 347 ?g/L for the surface-water sample. Experiments with mixtures of water, rocks, and chlorine indicated that reactions with the rock consumed chlorine and released significant amounts of organic carbon from the rock, increasing the DOC concentration in the water. The organic carbon in the rocks likely is associated with the secondary clay minerals that line vesicles and fractures in the rocks. THM concentrations were greatest, from 335 to 909 ?g/L, for surface water equilibrated with rock samples from Rattlesnake Hill. However, the concentration of chlorine required to produce these high THM concentrations ranged from 18 to 84 mg/L. The results of the experiments suggest that the amount of organic carbon released from the rocks during successive cycles of recharge, storage, and recovery of chlorinated surface water may be relatively small. The chlorine demand of the rocks is so large that all of the free chlorine in the entire volume of recharged water likely would be consumed by only a very small volume of the aquifer surrounding an injection well, or beneath an infiltration bed. The majority of the volume of the aquifer filled by the stored water likely would never come in contact with free chlorine, and the increases in concentration of DOC observed in these experiments likely would occur in a very small volume of the stored water. For this reason, increases in concentration of THMs for the entire volume of water stored also likely would be considerably less than those measured in these experiments. To test this hypothesis, additional laboratory experiments using varying levels of chlorination, varying lengths of reaction periods, and repeated cycles of chlorination would be useful. A field experiment made at a small scale in an isolated part of the basalt aquifer would aid in the design of an operational system.
Relationships between data from Rock-Eval pyrolysis and proximate, ultimate, petrographic, and physical analyses of 142 diverse U.S. coal samples

USGS Publications Warehouse

Bostick, N.H.; Daws, T.A.

1994-01-01

Basic research on coal and oil shale led to automated pyrolysis analysis of petroleum source rocks; most widely used is the Rock-Eval equipment. In order to interpret Rock-Eval analyses in relation to traditional coal data, we analyzed 142 commercial coals with diverse rank, age, maceral and sulfur contents, for most regions of the United States. We compared the Rock-Eval data with traditional industrial coal data, including volatile matter, calorific value, hydrogen and oxygen content, free swelling index, and vitrinite reflectance. We found: (1) there is a close relationship between Tmax and vitrinite reflectance in the ranges 420-590??C Tmax and 0.4-3%Romax of most coals. (2) A close relationship between Tmax and volatile matter (%VM) extends through the entire sample range, including low-rank samples with 35-70% VM, a range where %VM is not considered to be a useful rank parameter. (3) TOC of medium- and high-rank coals is seriously under-measured by Rock-Eval; TOC of low-rank coals (less than 0.8%Romax) is close to "dry basis" carbon from ultimate analysis. (4) The direct relationships between oxygen index (OI) and %O and between hydrogen index (HI) and %H are clear, though only broadly defined. However, there is virtually no band of concentrated data points on the HI versus OI pseudo-Van Krevelen diagram comparable to the "development line" on the H/C versus O/C diagram. (5) There are systematic relationships between Rock-Eval and industrial coal parameters such as calorific value and FSI, but much standardization would be needed before Rock-Eval could find a place in the coal industry. Tests with blends of coal and quartz sand and with various loads of coal alone showed that the amount of organic matter in the Rock-Eval load greatly influences results. Total load in the crucible, if largely inert, plays a small role, however. Increasing absolute or relative coal content causes under-evaluation of Rock-Eval TOC and over-rating of hydrogen. Blends of several coals yielded hydrogen and oxygen indexes related proportionally to the properties of the individual coals, but Tmax is not raised by addition of high-rank coal until over 40% is added. ?? 1994.
Reassessing the Evidence for the Earliest Traces of Life

NASA Technical Reports Server (NTRS)

vanZullen, Mark A.; Lepland, Alve; Arrhenlus, Gustaf

2002-01-01

The isotopic composition of graphite is commonly used as a biomarker in the oldest (>3.5 Gyr ago) highly metamorphosed terrestrial rocks. Earlier studies on isotopic characteristics of graphite occurring in rocks of the approximately 3.8-Gyr-old Isua supracrustal belt (ISB) in southern West Greenland have suggested the presence of a vast microbial ecosystem in the early Archean. This interpretation, however, has to be approached with extreme care. Here we show that graphite occurs abundantly in secondary carbonate veins in the ISB that are formed at depth in the crust by injection of hot fluids reacting with older crustal rocks (metasomatism). During these reactions, graphite forms from the disproportionation of Fe(II)-bearing carbonates at high temperature. These metasomatic rocks, which clearly lack biological relevance, were earlier thought to be of sedimentary origin and their graphite association provided the basis for inferences about early life. The new observations thus call for a reassessment of previously presented evidence for ancient traces of life in the highly metamorphosed Early Archaean rock record.
cyclostratigraphy, sequence stratigraphy and organic matter accumulation mechanism

NASA Astrophysics Data System (ADS)

Cong, F.; Li, J.

2016-12-01

The first member of Maokou Formation of Sichuan basin is composed of well preserved carbonate ramp couplets of limestone and marlstone/shale. It acts as one of the potential shale gas source rock, and is suitable for time-series analysis. We conducted time-series analysis to identify high-frequency sequences, reconstruct high-resolution sedimentation rate, estimate detailed primary productivity for the first time in the study intervals and discuss organic matter accumulation mechanism of source rock under sequence stratigraphic framework.Using the theory of cyclostratigraphy and sequence stratigraphy, the high-frequency sequences of one outcrop profile and one drilling well are identified. Two third-order sequences and eight fourth-order sequences are distinguished on outcrop profile based on the cycle stacking patterns. For drilling well, sequence boundary and four system tracts is distinguished by "integrated prediction error filter analysis" (INPEFA) of Gamma-ray logging data, and eight fourth-order sequences is identified by 405ka long eccentricity curve in depth domain which is quantified and filtered by integrated analysis of MTM spectral analysis, evolutive harmonic analysis (EHA), evolutive average spectral misfit (eASM) and band-pass filtering. It suggests that high-frequency sequences correlate well with Milankovitch orbital signals recorded in sediments, and it is applicable to use cyclostratigraphy theory in dividing high-frequency(4-6 orders) sequence stratigraphy.High-resolution sedimentation rate is reconstructed through the study interval by tracking the highly statistically significant short eccentricity component (123ka) revealed by EHA. Based on sedimentation rate, measured TOC and density data, the burial flux, delivery flux and primary productivity of organic carbon was estimated. By integrating redox proxies, we can discuss the controls on organic matter accumulation by primary production and preservation under the high-resolution sequence stratigraphic framework. Results show that high average organic carbon contents in the study interval are mainly attributed to high primary production. The results also show a good correlation between high organic carbon accumulation and intervals of transgression.
Geologic map showing springs rich in carbon dioxide or or chloride in California

USGS Publications Warehouse

Barnes, Ivan; Irwin, William P.; Gibson, H.A.

1975-01-01

Carbon dioxide- and chloride-rich springs occur in all geologic provinces in California, but are most abundant in the Coast Ranges and the Great Valley. The carbon-dioxide-rich springs issue mainly from Franciscan terrane; they also are rich in boron and are of the metamorphic type (White, 1957). Based on isotopic data, either the carbon dioxide or the water, or both, may be of metamorphic origin. Because of high magnesium values, the water of many of the carbon-dioxide-rich springs is thought to have passed through serpentinite. The chloride-rich waters are most common in rocks of the Great Valley sequence. Nearly all are more dilute than present-day sea water. The similarity in isotopic compositions of the metamorphic carbon-dioxide-rich water and the chloride-rich water may indicate a similar extent of water-rock interaction.
Reservoir characterization of the Upper Jurassic geothermal target formations (Molasse Basin, Germany): role of thermofacies as exploration tool

NASA Astrophysics Data System (ADS)

Homuth, S.; Götz, A. E.; Sass, I.

2015-06-01

The Upper Jurassic carbonates of the southern German Molasse Basin are the target of numerous geothermal combined heat and power production projects since the year 2000. A production-orientated reservoir characterization is therefore of high economic interest. Outcrop analogue studies enable reservoir property prediction by determination and correlation of lithofacies-related thermo- and petrophysical parameters. A thermofacies classification of the carbonate formations serves to identify heterogeneities and production zones. The hydraulic conductivity is mainly controlled by tectonic structures and karstification, whilst the type and grade of karstification is facies related. The rock permeability has only a minor effect on the reservoir's sustainability. Physical parameters determined on oven-dried samples have to be corrected, applying reservoir transfer models to water-saturated reservoir conditions. To validate these calculated parameters, a Thermo-Triaxial-Cell simulating the temperature and pressure conditions of the reservoir is used and calorimetric and thermal conductivity measurements under elevated temperature conditions are performed. Additionally, core and cutting material from a 1600 m deep research drilling and a 4850 m (total vertical depth, measured depth: 6020 m) deep well is used to validate the reservoir property predictions. Under reservoir conditions a decrease in permeability of 2-3 magnitudes is observed due to the thermal expansion of the rock matrix. For tight carbonates the matrix permeability is temperature-controlled; the thermophysical matrix parameters are density-controlled. Density increases typically with depth and especially with higher dolomite content. Therefore, thermal conductivity increases; however the dominant factor temperature also decreases the thermal conductivity. Specific heat capacity typically increases with increasing depth and temperature. The lithofacies-related characterization and prediction of reservoir properties based on outcrop and drilling data demonstrates that this approach is a powerful tool for exploration and operation of geothermal reservoirs.
Archean cherts: field, petrographic and geochemical criteria to determine their origin

NASA Astrophysics Data System (ADS)

Ledevin, Morgane; Arndt, Nicholas T.; Simionovici, Alexandre

2013-04-01

Archean cherts provide valuable information about conditions on the sea floor during the early history of Earth. We conducted field, petrological and geochemical studies on examples from different environments in the Barberton Greenstone Belt (3.2-3.5 Ga), South Africa, with the aim of improving our understanding of these enigmatic rocks. We distinguish three different origins for cherts: direct precipitation from seawater (C-cherts); precipitation in fractures from silica-rich fluids (F-cherts); and replacement of preexisting rocks (silicification) either at or near the surface (S-cherts). The three types were distinguished using a combination of sedimentary and deformation structures, petrological observations (RAMAN, electron microprobe, X-Ray microfluorescence, cathodoluminescence) and geochemical data. C-cherts best record the composition and physical conditions in primitive oceans and the depositional environment because they precipitated from seawater. Based on sedimentary structures, we show that the silica was deposited as a siliceous ooze or amorphous gel on the seafloor, with variable precipitation rates that depend on the amount and nature of co-precipitated phases (called here the "contaminant"), such as detrital grains, carbonates, carbonaceous matter and oxides. We observe a complex rheology of C-cherts, which show both ductile to brittle deformation structures, sometimes in the same layer. We infer that the cherts underwent extremely rapid diagenetic induration at or near the surface, a process that proceeded faster when contaminants are lacking. Geochemical data (ICP-MS/ICP-AES) indicate that whole rock chemistries are dominated by the contaminant phases. Detrital grains with continental signatures dominate the compositions of cherts in the turbidite sequence of the Komati River whereas carbonates preserving modern, seawater-like compositions control the compositions of cherts of Fig Tree Fm in the Barite Valley. The silica minerals do not contribute significantly to the trace-element composition, but acts as a diluent. Buck Reef cherts have extremely low contents of most trace elements due to low contents of detrital minerals and carbonates. S-cherts result from the silicification of preexisting rocks: under the action of circulating fluids, primary minerals are replaced by silica minerals and the porosity of the protolith is significantly reduced. Such process occurs even at the surface and persist downward the sedimentary units until after the rocks are indurated. F-cherts were observed in the Barite Valley, where chert dykes cross-cut surrounding units at high angle. The fractures often display jigsaw-puzzle textures, suggesting hydraulic fracturation, and their near-vertical orientation points to emplacement at shallow levels in the sediment pile. The dykes are filled with a black chert that contains variable amounts of host rock fragments that vary in shape (angular to rounded) and size (dm to µm). They control the whole-rock chemistry of cherts, and obscure the chemical composition of the primary, precipitating fluid. We believe that this fluid had a thixotropic behavior, i.e. it was fluid enough during the intrusion to fill very fine <1mm fractures but viscous enough when the velocity decreased to suspend decimetric host rock fragments. Based on our observations, we conclude that (1) field and petrological studies are more reliable than geochemical analyses for the recognition of various chert types; (2) the composition of cherts strongly depends on the type and amount of mineral phases other than silica, especially clays and carbonates; (3) C-cherts might be more abundant than previously thought and deposited as an amorphous, siliceous gel onto the seafloor before being rapidly indurated.
A New Biomarker Proxy for Palaeo-pCO2 Reconstruction in Ancient Sediments

NASA Astrophysics Data System (ADS)

Pancost, R. D.; Magness, S.; Maxwell, J. R.

2001-12-01

The carbon isotopic composition of marine organic matter has commonly been used in chemostratigraphy or as a proxy for ancient pCO2 levels. Both of these goals require that the source of organic matter be well defined, and in the case of palaeo-pCO2 investigations, the organic matter must be derived ultimately from aquatic photoautotrophs. However, additional sources, including terrestrial biomass, heterotrophs, or bacteria, can also contribute to total organic carbon (TOC). In the past decade, numerous workers have attempted to refine organic carbon isotope records using the isotopic composition of individual compounds (biomarkers) rather than the TOC. The appeal of this approach is that by examining specific biomarkers, a signal diagnostic for photoautotrophic organisms can be obtained. For compound-specific isotope analyses to be most effective, the compounds analysed must have a relatively specific source. Among the most commonly used biomarkers in palaeo-pCO2 investigations are alkenones, long-chain ketones derived exclusively from certain species of haptophyte algae. However, alkenones are absent in rocks older than the Jurassic and either absent or present in low abundances in rocks older than the Miocene. Thus, in older rocks, other biomarkers, including steranes (derived from eukaryotic sterols), phytane (presumably derived from chlorophyll), and n-alkanes (derived from algal macromolecules), are used. Unfortunately, these compounds can have alternative sources and become less reliable as isotopic proxies for photoautotrophs with increasing thermal maturity and complexity of the hydrocarbon distribution. Here we propose the use of a maleimides (1H-pyrrole-2,5-diones) as a new biomarker class for evaluating past changes in photoautotroph carbon isotopic compositions. Maleimides have three key advantages over other biomarkers in ancient rocks. First, they are degradation products of chlorophyll and have no known alternative origins in marine sediments. Second, because of their unique structure, they can be readily isolated from other organic components facilitating the determination of accurate carbon isotope ratios. Finally, the pyrrole structure is relatively stable insuring that maleimides survive even in thermally mature rocks. We have applied the analysis of maleimides to investigations of sediments from the Kupferschiefer (Permian), Vena del Gesso (Messinian) and Livello Bonarelli (Cenomanian-Turonian boundary) formations. In all three cases, the carbon isotopic compositions of selected maleimides exhibit shifts predicted by either carbonate or other biomarker carbon isotope profiles.
Shale-brine-CO2 interactions and the long-term stability of carbonate-rich shale caprock

NASA Astrophysics Data System (ADS)

Ilgen, A.; Aman, M.; Espinoza, D. N.; Rodriguez, M. A.; Griego, J.; Dewers, T. A.; Feldman, J.; Stewart, T.; Choens, R. C., II

2017-12-01

Geological carbon storage (GCS) requires an impermeable caprock (e.g., shale) that prevents the upward migration and escape of carbon dioxide (CO2) from the subsurface. Geochemical alteration can occur at the caprock-reservoir rock interface, which could lead to the altering of the rock's mechanical properties, compromising the seal. We performed laboratory experiments on Mancos shale to quantify the coupled chemical-mechanical response of carbonate-rich shale in CO2-brine mixtures at conditions typical to GCS. We constructed geochemical models, calibrated them using laboratory results, and extended to time scales required for GCS. We observed the dissolution of calcite and kaolinite and the precipitation of gypsum and amorphous aluminum (hydr)oxide following the introduction of CO2. To address whether this mineral alteration causes changes in micro-mechanical properties, we examined altered Mancos shale using micro-mechanical (scratch) testing, measuring the scratch toughness of mm-scale shale lithofacies. The quartz-rich regions of the Mancos shale did not show significant changes in scratch toughness following 1-week alteration in a CO2-brine mixture. However, the scratch toughness of the calcite-rich, originally softer regions decreased by about 50%. These observations illustrate a coupled and localized chemical-mechanical response of carbonate-rich shale to the injection of CO2. This suggests a localized weakening of the caprock may occur, potentially leading to the development of preferential flow paths. The identification of vulnerable lithofacies within caprock and a characterization of mineralogical heterogeneity is imperative at prospective GCS sites. Sandia National Laboratories is a multimission laboratory managed and operated by National Technology and Engineering Solutions of Sandia, LLC., a wholly owned subsidiary of Honeywell International, Inc., for the U.S. Department of Energy's National Nuclear Security Administration under contract DE-NA-0003525.
[Modeling the Influencing Factors of Karstification and Karst Carbon Cycle in Laboratory].

PubMed

Zhao, Rui-yi; Lü, Xian-fu; Duan, Yi-fan

2015-08-01

To analyze the influencing factors of karstification and karst carbon cycle, a simulation experiment was carried out and 6 soil columns were designed. The results showed that the content of H2O4, hydrodynamic condition and thickness of the soil had important influence on karstification and karst carbon cycle. For the soil columns which were covered by the same thickness of soil, the concentrations of Ca2+ + Mg2+ and SO4(2-) followed the order of B20-2 > B20-1 > B20-3, B50-2 > B50-1 > B50-3. This meant that input of H2SO4 enhanced the karstification and increasing infiltration water had significant dilution effect on the chemical properties. For the soil columns with different thickness of soil but with the same slag pile and hydrodynamic conditions, the concentrations of Ca2+ + Mg2+ and SO4(2-) followed the order of B50-1 > B20-1, B50-2 > B20-2, B50-3 > B20-3. It was demonstrated that more carbonate rock was dissolved under the thick soil columns. In addition, the net consumption of CO2 mainly depended on the content of H2SO4 in this experiment due to slight contribution of H2CO3 to carbonate rock dissolution. More content of H2SO4 brought about less net consumption of C02, but B50-2 was an exception. Organic matter and other nutrients might be input into deep soil with the slag pile, and they promoted the production of soil C)2. Therefore, more CO2 was consumed due to the increased contribution of H2CO to karstification.
One-carbon (bio ?) Geochemistry in Subsurface Waters of the Serpentinizing Coast Range Ophiolite

NASA Technical Reports Server (NTRS)

Hoehler, Tori M.; Mccollom, Tom; Schrenk, Matt; Cardace, Dawn

2011-01-01

Serpentinization - the aqueous alteration of ultramafic rocks - typically imparts a highly reducing and alkaline character to the reacting fluids. In turn, these can influence the speciation and potential for metabolism of one-carbon compounds in the system. We examined the aqueous geochemistry and assessed the biological potential of one-carbon compounds in the subsurface of the McLaughlin Natural Reserve (Coast Range Ophiolite, California, USA). Fluids from wells sunk at depths of 25-90 meters have pH values ranging from 9.7 to 11.5 and dissolved inorganic carbon (DIC concentrations) generally below 60 micromolar. Methane is present at concentrations up to 1.3 millimolar (approximately one-atmosphere saturation), and hydrogen concentrations are below 15 nanomolar, suggesting active consumption of H2 and production of CH4. However, methane production from CO2 is thermodynamically unfavorable under these conditions. Additionally, the speciation of DIC predominantly into carbonate at these high pH values creates a problem of carbon availability for any organisms that require CO2 (or bicarbonate) for catabolism or anabolism. A potential alternative is carbon monoxide, which is present in these waters at concentrations 2000-fold higher than equilibrium with atmospheric CO. CO is utilized in a variety of metabolisms, including methanogenesis, and bioavailability is not adversely affected by pH-dependent speciation (as for DIC). Methanogenesis from CO under in situ conditions is thermodynamically favorable and would satisfy biological energy requirements with respect to both Gibbs Energy yield and power.
Metal release from sandstones under experimentally and numerically simulated CO2 leakage conditions.

PubMed

Kirsch, Katie; Navarre-Sitchler, Alexis K; Wunsch, Assaf; McCray, John E

2014-01-01

Leakage of CO2 from a deep storage formation into an overlying potable aquifer may adversely impact water quality and human health. Understanding CO2-water-rock interactions is therefore an important step toward the safe implementation of geologic carbon sequestration. This study targeted the geochemical response of siliclastic rock, specifically three sandstones of the Mesaverde Group in northwestern Colorado. To test the hypothesis that carbonate minerals, even when present in very low levels, would be the primary source of metals released into a CO2-impacted aquifer, two batch experiments were conducted. Samples were reacted for 27 days with water and CO2 at partial pressures of 0.01 and 1 bar, representing natural background levels and levels expected in an aquifer impacted by a small leakage, respectively. Concentrations of major (e.g., Ca, Mg) and trace (e.g., As, Ba, Cd, Fe, Mn, Pb, Sr, U) elements increased rapidly after CO2 was introduced into the system, but did not exceed primary Maximum Contaminant Levels set by the U.S. Environmental Protection Agency. Results of sequential extraction suggest that carbonate minerals, although volumetrically insignificant in the sandstone samples, are the dominant source of mobile metals. This interpretation is supported by a simple geochemical model, which could simulate observed changes in fluid composition through CO2-induced calcite and dolomite dissolution.
Stable solid and aqueous H2CO3 from CO2 and H2O at high pressure and high temperature

NASA Astrophysics Data System (ADS)

Wang, Hongbo; Zeuschner, Janek; Eremets, Mikhail; Troyan, Ivan; Willams, Jonathan

2016-01-01

Carbonic acid (H2CO3) forms in small amounts when CO2 dissolves in H2O, yet decomposes rapidly under ambient conditions of temperature and pressure. Despite its fleeting existence, H2CO3 plays an important role in the global carbon cycle and in biological carbonate-containing systems. The short lifetime in water and presumed low concentration under all terrestrial conditions has stifled study of this fundamental species. Here, we have examined CO2/H2O mixtures under conditions of high pressure and high temperature to explore the potential for reaction to H2CO3 inside celestial bodies. We present a novel method to prepare solid H2CO3 by heating CO2/H2O mixtures at high pressure with a CO2 laser. Furthermore, we found that, contrary to present understanding, neutral H2CO3 is a significant component in aqueous CO2 solutions above 2.4 GPa and 110 °C as identified by IR-absorption and Raman spectroscopy. This is highly significant for speciation of deep C-O-H fluids with potential consequences for fluid-carbonate-bearing rock interactions. As conditions inside subduction zones on Earth appear to be most favorable for production of aqueous H2CO3, a role in subduction related phenomena is inferred.
Stable solid and aqueous H2CO3 from CO2 and H2O at high pressure and high temperature

PubMed Central

Wang, Hongbo; Zeuschner, Janek; Eremets, Mikhail; Troyan, Ivan; Willams, Jonathan

2016-01-01

Carbonic acid (H2CO3) forms in small amounts when CO2 dissolves in H2O, yet decomposes rapidly under ambient conditions of temperature and pressure. Despite its fleeting existence, H2CO3 plays an important role in the global carbon cycle and in biological carbonate-containing systems. The short lifetime in water and presumed low concentration under all terrestrial conditions has stifled study of this fundamental species. Here, we have examined CO2/H2O mixtures under conditions of high pressure and high temperature to explore the potential for reaction to H2CO3 inside celestial bodies. We present a novel method to prepare solid H2CO3 by heating CO2/H2O mixtures at high pressure with a CO2 laser. Furthermore, we found that, contrary to present understanding, neutral H2CO3 is a significant component in aqueous CO2 solutions above 2.4 GPa and 110 °C as identified by IR-absorption and Raman spectroscopy. This is highly significant for speciation of deep C–O–H fluids with potential consequences for fluid-carbonate-bearing rock interactions. As conditions inside subduction zones on Earth appear to be most favorable for production of aqueous H2CO3, a role in subduction related phenomena is inferred. PMID:26813580
Stable solid and aqueous H2CO3 from CO2 and H2O at high pressure and high temperature.

PubMed

Wang, Hongbo; Zeuschner, Janek; Eremets, Mikhail; Troyan, Ivan; Willams, Jonathan

2016-01-27

Carbonic acid (H2CO3) forms in small amounts when CO2 dissolves in H2O, yet decomposes rapidly under ambient conditions of temperature and pressure. Despite its fleeting existence, H2CO3 plays an important role in the global carbon cycle and in biological carbonate-containing systems. The short lifetime in water and presumed low concentration under all terrestrial conditions has stifled study of this fundamental species. Here, we have examined CO2/H2O mixtures under conditions of high pressure and high temperature to explore the potential for reaction to H2CO3 inside celestial bodies. We present a novel method to prepare solid H2CO3 by heating CO2/H2O mixtures at high pressure with a CO2 laser. Furthermore, we found that, contrary to present understanding, neutral H2CO3 is a significant component in aqueous CO2 solutions above 2.4 GPa and 110 °C as identified by IR-absorption and Raman spectroscopy. This is highly significant for speciation of deep C-O-H fluids with potential consequences for fluid-carbonate-bearing rock interactions. As conditions inside subduction zones on Earth appear to be most favorable for production of aqueous H2CO3, a role in subduction related phenomena is inferred.
Unroofing history of Late Paleozoic magmatic arcs within the ``Turan Plate'' (Tuarkyr, Turkmenistan)

NASA Astrophysics Data System (ADS)

Garzanti, E.; Gaetani, M.

2002-07-01

Stratigraphic, sedimentologic and petrographic data collected on the Kizilkaya sedimentary succession (Western Turkmenistan) demonstrate that the "Turan Plate" consists in fact of an amalgamation of Late Paleozoic to Triassic continental microblocks separated by ocean sutures. In the Kizilkaya area, an ophiolitic sequence including pyroxenite, gabbro, pillow basalt and chert, interpreted as the oceanic crust of a back-arc or intra-arc basin, is tectonically juxtaposed against volcaniclastic redbeds documenting penecontemporaneous felsic arc magmatism (Amanbulak Group). A collisional event took place around ?mid-Carboniferous times, when oceanic rocks underwent greenschist-facies metamorphism and a thick volcaniclastic wedge, with pyroclastic rocks interbedded in the lower part, accumulated (Kizilkaya Formation). The climax of orogenic activity is testified by arid fanglomerates shed from the rapid unroofing of a continental arc sequence, including Middle-Upper Devonian back-reef carbonates and cherts, and the underlying metamorphic and granitoid basement rocks (Yashmu Formation). After a short period of relative quiescence, renewed tectonic activity is indicated by a conglomeratic sequence documenting erosion of a sedimentary and metasedimentary succession including chert, sandstone, slate and a few carbonates. A final stage of rhyolitic magmatism took place during rapid unroofing of granitoid basement rocks (Kizildag Formation). Such a complex sequence of events recorded by the Kizilkaya episutural basin succession documents the stepwise assemblage of magmatic arcs and continental fragments to form the Turan microblock collage during the Late Paleozoic. Evolution of detrital modes is compatible with that predicted for juvenile to accreted and unroofed crustal blocks. The deposition of braidplain lithic arkoses in earliest Triassic time indicates that strong subsidence continued after the end of the volcanic activity, possibly in retroarc foreland basin settings. The occurrence of transgressive coquinas yielding endemic ammonoids ( Dorikranites) characteristic of the whole Caspian area suggests proximity to the southern margin of the newly formed Eurasian continent in the late Early Triassic. The Late Triassic Eo-Cimmerian Orogeny caused only mild tilting and rejuvenation of the underlying succession in the study area. Only at this time were the Turan blocks, a series of Indonesian-type terranes comprised between the Mashad Paleo-Tethys Suture in the south and the Mangyshlak belt in the north, finally incorporated into the Eurasian landmass.
Analysis of Ground-Water Levels and Associated Trends in Yucca Flat, Nevada Test Site, Nye County, Nevada, 1951-2003

DOE Office of Scientific and Technical Information (OSTI.GOV)

J.M. Fenelon

2005-10-05

Almost 4,000 water-level measurements in 216 wells in the Yucca Flat area from 1951 to 2003 were quality assured and analyzed. An interpretative database was developed that describes water-level conditions for each water level measured in Yucca Flat. Multiple attributes were assigned to each water-level measurement in the database to describe the hydrologic conditions at the time of measurement. General quality, temporal variability, regional significance, and hydrologic conditions are attributed for each water-level measurement. The database also includes narratives that discuss the water-level history of each well. Water levels in 34 wells were analyzed for variability and for statistically significantmore » trends. An attempt was made to identify the cause of many of the water-level fluctuations or trends. Potential causes include equilibration following well construction or development, pumping in the monitoring well, withdrawals from a nearby supply well, recharge from precipitation, earthquakes, underground nuclear tests, land subsidence, barometric pressure, and Earth tides. Some of the naturally occurring fluctuations in water levels may result from variations in recharge. The magnitude of the overall water-level change for these fluctuations generally is less than 2 feet. Long-term steady-state hydrographs for most of the wells open to carbonate rock have a very similar pattern. Carbonate-rock wells without the characteristic pattern are directly west of the Yucca and Topgallant faults in the southwestern part of Yucca Flat. Long-term steady-state hydrographs from wells open to volcanic tuffs or the Eleana confining unit have a distinctly different pattern from the general water-level pattern of the carbonate-rock aquifers. Anthropogenic water-level fluctuations were caused primarily by water withdrawals and nuclear testing. Nuclear tests affected water levels in many wells. Trends in these wells are attributed to test-cavity infilling or the effects of depressurization following nuclear testing. The magnitude of the overall water-level change for wells with anthropogenic trends can be large, ranging from several feet to hundreds of feet. Vertical water-level differences at 27 sites in Yucca Flat with multiple open intervals were compared. Large vertical differences were noted in volcanic rocks and in boreholes where water levels were affected by nuclear tests. Small vertical differences were noted within the carbonate-rock and valley-fill aquifers. Vertical hydraulic gradients generally are downward in volcanic rocks and from pre-Tertiary clastic rocks toward volcanic- or carbonate-rock units.« less
Analysis of ground-water levels and associated trends in Yucca Flat, Nevada Test Site, Nye County, Nevada, 1951-2003

USGS Publications Warehouse

Fenelon, Joseph M.

2005-01-01

Almost 4,000 water-level measurements in 216 wells in the Yucca Flat area from 1951 to 2003 were quality assured and analyzed. An interpretative database was developed that describes water-level conditions for each water level measured in Yucca Flat. Multiple attributes were assigned to each water-level measurement in the database to describe the hydrologic conditions at the time of measurement. General quality, temporal variability, regional significance, and hydrologic conditions are attributed for each water-level measurement. The database also includes narratives that discuss the water-level history of each well. Water levels in 34 wells were analyzed for variability and for statistically significant trends. An attempt was made to identify the cause of many of the water-level fluctuations or trends. Potential causes include equilibration following well construction or development, pumping in the monitoring well, withdrawals from a nearby supply well, recharge from precipitation, earthquakes, underground nuclear tests, land subsidence, barometric pressure, and Earth tides. Some of the naturally occurring fluctuations in water levels may result from variations in recharge. The magnitude of the overall water-level change for these fluctuations generally is less than 2 feet. Long-term steady-state hydrographs for most of the wells open to carbonate rock have a very similar pattern. Carbonate-rock wells without the characteristic pattern are directly west of the Yucca and Topgallant faults in the southwestern part of Yucca Flat. Long-term steady-state hydrographs from wells open to volcanic tuffs or the Eleana confining unit have a distinctly different pattern from the general water-level pattern of the carbonate-rock aquifers. Anthropogenic water-level fluctuations were caused primarily by water withdrawals and nuclear testing. Nuclear tests affected water levels in many wells. Trends in these wells are attributed to test-cavity infilling or the effects of depressurization following nuclear testing. The magnitude of the overall water-level change for wells with anthropogenic trends can be large, ranging from several feet to hundreds of feet. Vertical water-level differences at 27 sites in Yucca Flat with multiple open intervals were compared. Large vertical differences were noted in volcanic rocks and in boreholes where water levels were affected by nuclear tests. Small vertical differences were noted within the carbonate-rock and valley-fill aquifers. Vertical hydraulic gradients generally are downward in volcanic rocks and from pre-Tertiary clastic rocks toward volcanic- or carbonate-rock units.

Use of the Biotic Ligand Model to predict metal toxicity to aquatic biota in areas of differing geology

USGS Publications Warehouse

Smith, Kathleen S.

2005-01-01

This work evaluates the use of the biotic ligand model (BLM), an aquatic toxicity model, to predict toxic effects of metals on aquatic biota in areas underlain by different rock types. The chemical composition of water, soil, and sediment is largely derived from the composition of the underlying rock. Geologic source materials control key attributes of water chemistry that affect metal toxicity to aquatic biota, including: 1) potentially toxic elements, 2) alkalinity, 3) total dissolved solids, and 4) soluble major elements, such as Ca and Mg, which contribute to water hardness. Miller (2002) compiled chemical data for water samples collected in watersheds underlain by ten different rock types, and in a mineralized area in western Colorado. He found that each rock type has a unique range of water chemistry. In this study, the ten rock types were grouped into two general categories, igneous and sedimentary. Water collected in watersheds underlain by sedimentary rock has higher mean pH, alkalinity, and calcium concentrations than water collected in watersheds underlain by igneous rock. Water collected in the mineralized area had elevated concentrations of calcium and sulfate in addition to other chemical constituents. Miller's water-chemistry data were used in the BLM (computer program) to determine copper and zinc toxicity to Daphnia magna. Modeling results show that waters from watersheds underlain by different rock types have characteristic ranges of predicted LC 50 values (a measurement of aquatic toxicity) for copper and zinc, with watersheds underlain by igneous rock having lower predicted LC 50 values than watersheds underlain by sedimentary rock. Lower predicted LC 50 values suggest that aquatic biota in watersheds underlain by igneous rock may be more vulnerable to copper and zinc inputs than aquatic biota in watersheds underlain by sedimentary rock. For both copper and zinc, there is a trend of increasing predicted LC 50 values with increasing dissolved organic carbon (DOC) concentrations. Predicted copper LC 50 values are extremely sensitive to DOC concentrations, whereas alkalinity appears to have an influence on zinc toxicity at alkalinities in excess of about 100 mg/L CaCO 3 . These findings show promise for coupling the BLM (computer program) with measured water-chemistry data to predict metal toxicity to aquatic biota in different geologic settings and under different scenarios. This approach may ultimately be a useful tool for mine-site planning, mitigation and remediation strategies, and ecological risk assessment.
CO2 production by mechanical stress on carbonate rocks and its implications for natural hazards assessment

NASA Astrophysics Data System (ADS)

Italiano, Francesco; Pizzullo, Sonia; Plescia, Paolo

2010-05-01

The distribution of known CO2 discharges generally coincides with the on-land segments of major linear zones of seismicity throughout the world, showing the strong correlation between natural degassing and earthquakes. On the other hand, aftershocks of large earthquakes have been attributed to the coseismic release of trapped, high-pressure CO2-dominated fluids propagating through damaged zones created by the main shock thus underlining the role of the fluids as "agents" able to generate overpressures and reactivate fault segments inducing earthquakes. Recent experimental results have demonstrated that CO2 can be produced by mechanical stress applied on carbonate rocks sometimes requiring a relatively low energy amount. As a result, crustal volatiles can be produced due to high-pressure, mechanical stresses at moderate levels within the crust. Experiments, whereby different types of carbonate rocks (natural and synthetic) have been milled, have shown that carbonates release CO2 systematically and reproducibly leaving little doubt that carbonate rock located in shallow parts of the crust may undergo structural break-down to form CO2, particularly in the presence of accessory phases such as clays. Such a process allows several natural systems (e.g. active faults in limestones) to become significant CO2 producer when mechanical stress is applied. The possibility of assessing the linkage between variations in geochemical tracers and the onset of seismic activity, is a topical research activity of meaningful societal relevance and contributes to understand some processes related to the seismogenesis, thus to the largest natural hazard for the humankind. As such, monitoring CO2 over seismic-prone areas located in carbonate rocks, may provide a better insight of the development of the seismogenic process and useful tools in understanding the response of volatiles to crustal perturbations. Moreover, since crustal deformation can also occur aseismically, and rock deformation may produce CO2 as a response to the applied mechanical stress, monitoring of CO2 discharges could be useful in the estimate the probability increase of an impending earthquake in a potentially hazardous seismic region. Laboratory results and field investigations carried out over the seismic-prone area of the Central Apennines provided the first results useful for practical applications in facing the natural hazards related to both seismic activity and release of hazardous gases.
The apollo 16 lunar samples: petrographic and chemical description.

PubMed

1973-01-05

The preliminary characterization of the rocks and soils returned from the Apollo 16 site has substantiated the inference that the lunar terra are commonly underlain by plagioclase-rich or anorthositic rocks. No evidence has been found for volcanic rocks underlying the regolith in the Apollo 16 region. In their place, we have found anorthositic rocks that are thoroughly modified by crushing and partial melting. The textural and chemical variations in these rocks provide some evidence for the existence of anorthositic complexes that have differentiated on a scale of tens to hundreds of meters. The occurrence of deep-seated or plutonic rocks in place of volcanic or pyroclastic materials at this site suggests that the inference from physiographic evidence that the latter materials are widespread in terra regions may be incorrect. Several additional, more specific conclusions derived from this preliminary examination are: 1) The combination of data from the Descartes region with data from the orbital x-ray fluorescence experiment indicates that some backside, highland regions are underlain by materials that consist of more than 80 percent plagioclase. 2) The soil or upper regolith between North Ray and South Ray has not been completely homogenized since the time of formation of these craters. 3) The chemistry of the soil indicates that rocks rich in potassium, uranium, and thorium, similar to those that prevail at the Fra Mauro site, are relatively abundant (10 to 20 percent) in the Descartes region. 4) The K/U ratio of the lunar crust is similar to that of the KREEP basalts. 5) The carbon content of the premare lunar crust is even lower than that of the mare volcanic rocks.
Permanganate diffusion and reaction in sedimentary rocks.

PubMed

Huang, Qiuyuan; Dong, Hailiang; Towne, Rachael M; Fischer, Timothy B; Schaefer, Charles E

2014-04-01

In situ chemical oxidation using permanganate has frequently been used to treat chlorinated solvents in fractured bedrock aquifers. However, in systems where matrix back-diffusion is an important process, the ability of the oxidant to migrate and treat target contaminants within the rock matrix will likely determine the overall effectiveness of this remedial approach. In this study, a series of diffusion experiments were performed to measure the permanganate diffusion and reaction in four different types of sedimentary rocks (dark gray mudstone, light gray mudstone, red sandstone, and tan sandstone). Results showed that, within the experimental time frame (~2 months), oxidant migration into the rock was limited to distances less than 500 μm. The observed diffusivities for permanganate into the rock matrices ranged from 5.3 × 10(-13) to 1.3 × 10(-11) cm(2)/s. These values were reasonably predicted by accounting for both the rock oxidant demand and the effective diffusivity of the rock. Various Mn minerals formed as surface coatings from reduction of permanganate coupled with oxidation of total organic carbon (TOC), and the nature of the formed Mn minerals was dependent upon the rock type. Post-treatment tracer testing showed that these Mn mineral coatings had a negligible impact on diffusion through the rock. Overall, our results showed that the extent of permanganate diffusion and reaction depended on rock properties, including porosity, mineralogy, and organic carbon. These results have important implications for our understanding of long-term organic contaminant remediation in sedimentary rocks using permanganate. Copyright © 2014 Elsevier B.V. All rights reserved.
Sinkhole susceptibility in carbonate rocks of the Apulian karst (southern Italy)

NASA Astrophysics Data System (ADS)

Di Santo, Antonio; Fazio, Nunzio L.; Fiore, Antonio; Lollino, Piernicola; Luisi, Michele; Miccoli, Maria N.; Pagliarulo, Rosa; Parise, Mario; Perrotti, Michele; Pisano, Luca; Spalluto, Luigi; Vennari, Carmela; Vessia, Giovanna

2016-04-01

Apulia region, the foreland of the southern Italian Apennines, is made up of a 6-7 km-thick succession of Mesozoic shallow-water limestones and dolostones, locally covered by thin and discontinuous Tertiary and Quaternary carbonate and clastic deposits. Due to their long subaerial exposure, the Mesozoic carbonate bedrock recorded the development in the subsurface of a dense network of karst cavities, mostly controlled by tectonic discontinuities. As a result, a strong susceptibility to natural sinkholes has to be recorded in Apulia. In addition, the possibility of occurrence of other problems related to the high number of man-made cavities has to be added in the region. A great variety of different typologies of artificial cavities (mostly excavated in the Plio-Pleistocene soft calcarenites) is actually present, including underground quarries, worship sites, oil mills, civilian settlements, etc. Overall, 2200 natural and 1200 artificial cavities, respectively, have been so far surveyed in Apulia. Following the urban development in the last century in Apulia, many of these cavities lie nowadays below densely populated neighborhoods, roads or communication routes. These conditions are at the origin of the main geomorphological hazard for the human society in Apulia, which requires a careful evaluation, aimed at protecting and safeguarding the human life, and at providing the necessary information for a correct land use planning and management. The importance of the sinkhole hazard is further testified by the worrying increase in the number of events during the last 5-6 years. In response to these situations, joint research activities were started by the Institute of Research for Hydrological Protection of the National Research Council (CNR-IRPI) and the Basin Authority of Apulia, aimed at several goals, that include (but are not limited to) the collection of information on natural and anthropogenic sinkholes in Apulia, the implementation of numerical analyses for modelling the instability processes, and the development of charts for a preliminary evaluation of the stability of underground caves. Two distinct approaches were established to take into account the different petrographic, structural and geotechnical features of both the hard and soft carbonate rocks. The approach dealing with hard carbonate rocks (where natural karst caves develop) is based on speleological and geometrical surveys of the caves and on an integrated geological and geomechanical characterization of the carbonate rock mass, aimed at individuating the main critical aspects of the karst caves in terms of likely effects on the society. On the other hand, the approach to verify the stability of soft rocks where artificial cavities have been excavated is mostly dependent upon the peculiar petrographic and geomechanical characteristics of the calcarenite rock mass, typically massive and unaffected by tectonic discontinuities. As a consequence, the traditional analytical methods of rock mass classification fail in these materials, since the rock strength of soft calcarenites is mostly dependent upon sediment texture, porosity type and distribution and degree of cementation. The fluid circulation into the rock mass is also important because the removal of the rock matrix may induce a rapid deterioration of the mechanical behaviour of the rock mass. The approach to the calcarenite is mostly based on the characterization of petrographic and geotechnical parameters by means of direct sampling from the rock walls and in situ surveys (wells, trenches, etc.). Through implementation of the two approaches, our goal is to reconstruct accurate geometrical, geological and geotechnical models for both natural caves and artificial cavities. These models will be useful also to plan specific monitoring activities in order to understand the development of underground instability, and the related evolution through the rock mass, possibly threatening the urban areas and infrastructures above.
Predictions of diagenetic reactions in the presence of organic acids

NASA Astrophysics Data System (ADS)

Harrison, Wendy J.; Thyne, Geoffrey D.

1992-02-01

Stability constants have been estimated for cation complexes with anions of monofunctional and difunctional acids (combinations of Ca, Mg, Fe, Al, Sr, Mn, U, Th, Pb, Cu, Zn with formate, acetate, propionate, oxalate, malonate, succinate, and salicylate) between 0 and 200°C. Difunctional acid anions form much more stable complexes than monofunctional acid anions with aluminum; the importance of the aluminum-acetate complex is relatively minor in comparison to aluminum oxalate and malonate complexes. Divalent metal cations such as Mg, Ca, and Fe form more stable complexes with acetate than with difunctional acid anions. Aluminum-oxalate can dominate the species distribution of aluminum under acidic pH conditions, whereas the divalent cation-acetate and oxalate complexes rarely account for more than 60% of the total dissolved cation, and then only in more alkaline waters. Mineral thermodynamic affinities were calculated using the reaction path model EQ3/6 for waters having variable organic acid anion (OAA) contents under conditions representative of those found during normal burial diagenesis. The following scenarios are possible: 1) K-feldspar and albite are stable, anorthite dissolves 2) All feldpars are stable 3) Carbonates can be very unstable to slightly unstable, but never increase in stability. Organic acid anions are ineffective at neutral to alkaline pH in modifying stabilities of aluminosilicate minerals whereas the anions are variably effective under a wide range of pH in modifying carbonate mineral stabilities. Reaction path calculations demonstrate that the sequence of mineral reactions occurring in an arkosic sandstone-fluid system is only slightly modified by the presence of OAA. A spectrum of possible sandstone alteration mineralogies can be obtained depending on the selected boundary conditions: EQ3/6 predictions include quartz overgrowth, calcite replacement of plagioclase, albitization of plagioclase, and the formation of porosity-occluding calcite cement, smectite, and illite, all of which are commonly documented in rocks. Under some circumstances, OAA-bearing waters are less effective at producing porosity in an arkosic sandstone than are OAA-free waters. In the scenarios modeled in this study the role of OAA in fluid-rock interactions is to contribute to the total alteration assemblage but not necessarily to dominate it, except under exceptional circumstances that might include, for example, hydrocarbon contaminant plumes in aquifers, wetland environments, and within hydrocarbon source-rocks.
Multi-scale image segmentation and numerical modeling in carbonate rocks

NASA Astrophysics Data System (ADS)

Alves, G. C.; Vanorio, T.

2016-12-01

Numerical methods based on computational simulations can be an important tool in estimating physical properties of rocks. These can complement experimental results, especially when time constraints and sample availability are a problem. However, computational models created at different scales can yield conflicting results with respect to the physical laboratory. This problem is exacerbated in carbonate rocks due to their heterogeneity at all scales. We developed a multi-scale approach performing segmentation of the rock images and numerical modeling across several scales, accounting for those heterogeneities. As a first step, we measured the porosity and the elastic properties of a group of carbonate samples with varying micrite content. Then, samples were imaged by Scanning Electron Microscope (SEM) as well as optical microscope at different magnifications. We applied three different image segmentation techniques to create numerical models from the SEM images and performed numerical simulations of the elastic wave-equation. Our results show that a multi-scale approach can efficiently account for micro-porosities in tight micrite-supported samples, yielding acoustic velocities comparable to those obtained experimentally. Nevertheless, in high-porosity samples characterized by larger grain/micrite ratio, results show that SEM scale images tend to overestimate velocities, mostly due to their inability to capture macro- and/or intragranular- porosity. This suggests that, for high-porosity carbonate samples, optical microscope images would be more suited for numerical simulations.
Increased forest ecosystem carbon and nitrogen storage from nitrogen rich bedrock.

PubMed

Morford, Scott L; Houlton, Benjamin Z; Dahlgren, Randy A

2011-08-31

Nitrogen (N) limits the productivity of many ecosystems worldwide, thereby restricting the ability of terrestrial ecosystems to offset the effects of rising atmospheric CO(2) emissions naturally. Understanding input pathways of bioavailable N is therefore paramount for predicting carbon (C) storage on land, particularly in temperate and boreal forests. Paradigms of nutrient cycling and limitation posit that new N enters terrestrial ecosystems solely from the atmosphere. Here we show that bedrock comprises a hitherto overlooked source of ecologically available N to forests. We report that the N content of soils and forest foliage on N-rich metasedimentary rocks (350-950 mg N kg(-1)) is elevated by more than 50% compared with similar temperate forest sites underlain by N-poor igneous parent material (30-70 mg N kg(-1)). Natural abundance N isotopes attribute this difference to rock-derived N: (15)N/(14)N values for rock, soils and plants are indistinguishable in sites underlain by N-rich lithology, in marked contrast to sites on N-poor substrates. Furthermore, forests associated with N-rich parent material contain on average 42% more carbon in above-ground tree biomass and 60% more carbon in the upper 30 cm of the soil than similar sites underlain by N-poor rocks. Our results raise the possibility that bedrock N input may represent an important and overlooked component of ecosystem N and C cycling elsewhere.
Cyclic transgressive and regressive sequences, Paleocene Suite, Sirte basin, Libya

DOE Office of Scientific and Technical Information (OSTI.GOV)

Abushagur, S.A.

1986-05-01

The Farrud lithofacies represent the main reservoir rock of the Ghani oil field and Western Concession Eleven of the Sirte basin, Libya. Eight microfacies are recognized in the Farrud lithofacies in the Ghani field area: (1) bryozoan-bioclastic (shallow, warm, normal marine shelf deposits); (2) micrite (suggesting quiet, low-energy conditions such as may have existed in a well-protected lagoon); (3) dasycladacean (very shallow, normal marine environment); (4) bioclastic (very shallow, normal marine environment with moderate to vigorous energy); (5) mgal (very shallow, normal marine environment in a shelf lagoon); (6) pelletal-skeletal (deposition within slightly agitated waters of a sheltered lagoon withmore » restricted circulation); (7) dolomicrite (fenestrate structures indicating a high intertidal environment of deposition); and (8) anhydrite (supratidal environment). The Paleocene suite of the Farrud lithofacies generally shows a prograding, regressive sequence of three facies: (1) supratidal facies, characterized by nonfossiliferous anhydrite, dolomite, and dolomitic pelletal carbonate mudstone; (2) intertidal to very shallow subtidal facies, characterized by fossiliferous, pelletal, carbonate mudstone and skeletal calcarenite; and (3) subtidal facies, characterized by a skeletal, pelletal, carbonate mudstone. Source rocks were primarily organic-rich shales overlying the Farrud reservoir rock. Porosity and permeability were developed in part by such processes as dolomitization, leaching, and fracturing in the two progradational, regressive carbonate facies. Hydrocarbons were trapped by a supratidal, anhydrite cap rock.« less
Rietveld analysis of X-ray powder diffraction patterns as a potential tool for the identification of impact-deformed carbonate rocks

NASA Astrophysics Data System (ADS)

Huson, S. A.; Foit, F. F.; Watkinson, A. J.; Pope, M. C.

2009-12-01

Previous X-ray powder diffraction (XRD) studies revealed that shock deformed carbonates and quartz have broader XRD patterns than those of unshocked samples. Entire XRD patterns, single peak profiles and Rietveld refined parameters of carbonate samples from the Sierra Madera impact crater, west Texas, unshocked equivalent samples from 95 miles north of the crater and the Mission Canyon Formation of southwest Montana and western Wyoming were used to evaluate the use of X-ray powder diffraction as a potential tool for distinguishing impact deformed rocks from unshocked and tectonically deformed rocks. At Sierra Madera dolostone and limestone samples were collected from the crater rim (lower shock intensity) and the central uplift (higher shock intensity). Unshocked equivalent dolostone samples were collected from well cores drilled outside of the impact crater. Carbonate rocks of the Mission Canyon Formation were sampled along a transect across the tectonic front of the Sevier and Laramide orogenic belts. Whereas calcite subjected to significant shock intensities at the Sierra Madera impact crater can be differentiated from tectonically deformed calcite from the Mission Canyon Formation using Rietveld refined peak profiles, weakly shocked calcite from the crater rim appears to be indistinguishable from the tectonically deformed calcite. In contrast, Rietveld analysis readily distinguishes shocked Sierra Madera dolomite from unshocked equivalent dolostone samples from outside the crater and tectonically deformed Mission Canyon Formation dolomite.
Paleomagnetic dating of the Cu-Zn-Pb Kupferschiefer deposit at Sangerhausen, Germany

NASA Astrophysics Data System (ADS)

Symons, D. T.; Kawasaki, K.; Walther, S.; Borg, G.

2010-12-01

Paleomagnetic and rock magnetic results are reported for the Cu-Zn-Pb Kupferschiefer mineralization at Sangerhausen, Germany. The mineralization is richest in the ~0.5 m thick Upper Permian (258±2 Ma) Kupferschiefer black marly shale (9 sites) and dies out over ~0.2 m in the underlying Weisliegend sandstones (3 sites) and overlying Zechstein carbonates (2 sites). Paleomagnetic and rock magnetic analysis were made on 205 specimens from 15 sites on the margin of the Sangerhausen Syncline. Except for the one site from fault zone gypsum, stable characteristic remanent magnetization (ChRM) directions were isolated in pyrrhotite with minor magnetite for the 14 sites using alternating field and thermal step demagnetization. Rock magnetic measurements show that the Kupferschiefer shale marks a redox front between the oxidized Weissliegend sandstones and non-oxidized Zechstein carbonates. A negative paleomagnetic fold test indicates that the ChRM postdates Jurassic fault block tilting. The ChRM directions from the 14 sites give a Late Jurassic paleopole at 149±3 Ma on the European apparent polar wander path. The observed age is significantly younger than the 254±6 Ma primary age of the associated red beds near Lubin in Poland, based on re-interpretation of the 1987 paleopole of Jowett et al. Overall the paleomagnetic results at Sangerhausen favour a very late diagenetic or epigenetic Late Jurassic origin for the Cu-Pb-Zn mineralization in the Kupferschiefer rather than the commonly proposed Late Permian syngenetic to mid-Triassic diagenetic origin.
Evaluation of multispectral middle infrared aircraft images for lithologic mapping the East Tintic Mountains, Utah( USA).

USGS Publications Warehouse

Kahle, A.B.; Rowan, L.C.

1980-01-01

Six channels of moultispectral middle infrared (8 to 14 micrometres) aircraft scanner data were acquired over the East Tintic mining district, Utah. The digital image data were computer processed to create a color-composite image based on principal component transformations. When combined with a visible and near infrared color-composite image from a previous flight, with limited field checking, it is possible to discriminate quartzite, carbonate rocks, quartz latitic and quartz monzonitic rocks, latitic and monzonitic rocks, silicified altered rocks, argillized altered rocks, and vegetation. -from Authors
Biostratigraphy and structure of paleozoic host rocks and their relationship to Carlin-type gold deposits in the Jerritt Canyon mining district, Nevada

USGS Publications Warehouse

Peters, S.G.; Armstrong, A.K.; Harris, A.G.; Oscarson, R.L.; Noble, P.J.

2003-01-01

The Jerritt Canyon mining district in the northern Independence Range, northern Nevada, contains multiple, nearly horizontal, thrust masses of platform carbonate rocks that are exposed in a series of north- to northeast-elongated, tectonic windows through rocks of the Roberts Mountains allochthon. The Roberts Mountains allochthon was emplaced during the Late Devonian to Early Mississippian Antler orogeny. These thrust masses contain structurally and stratigraphically controlled Carlin-type gold deposits. The gold deposits are hosted in tectonically truncated units of the Silurian to Devonian Hanson Creek and Roberts Mountains Formations that lie within structural slices of an Eastern assemblage of Cambrian to Devonian carbonate rocks. In addition, these multiply thrust-faulted and folded host rocks are structurally interleaved with Mississippian siliciclastic rocks and are overlain structurally by Cambrian to Devonian siliciclastic units of the Roberts Mountains allochthon. All sedimentary rocks were involved in thrusting, high-angle faulting, and folding, and some of these events indicate substantial late Paleozoic and/or Mesozoic regional shortening. Early Pennsylvanian and late Eocene dikes also intrude the sedimentary rocks. These rocks all were uplifted into a northeast-trending range by subsequent late Cenozoic Basin and Range faulting. Eocene sedimentary and volcanic rocks flank part of the range. Pathways of hydrothermal fluid flow and locations of Carlin-type gold orebodies in the Jerritt Canyon mining district were controlled by structural and host-rock geometries within specific lithologies of the stacked thrust masses of Eastern assemblage rocks. The gold deposits are most common proximal to intersections of northeast-striking faults, northwest-striking dikes, and thrust planes that lie adjacent to permeable stratigraphic horizons. The host stratigraphic units include carbonate sequences that contained primary intercrystalline permeability, which provided initial pathways for fluid flow and later served as precipitation sites for ore minerals. Alteration, during, and perhaps prior to mineralization, enhanced primary permeability by dissolution, by removal of calcite, and by formation of dolomite. Ore-stage sulfide minerals and alteration minerals commonly precipitated in pore spaces among dolomite grains. Microveinlets and microbrecciation in zones of intense alteration also provided networks of secondary permeability that further enhanced fluid flux and produced additional sites for ore deposition.
Evaluating CO2 mineralization capacity of sedimentary rock Using BCR sequential extraction procedures

NASA Astrophysics Data System (ADS)

Yang, Gang-Ting; Yu, Chi-Wen; Yang, Hsiao-Ming; Chiao, Chung-Hui; Yang, Ming-Wei

2015-04-01

To relief the high concentration of carbon dioxide in the atmosphere, carbon capture and storage (CCS) is gradually becoming an important concept to reduce greenhouse gas emissions. In IPCC Special Report on CCS, the storage mechanisms for geological formations are categorized into structural/stratigraphic, hydrodynamic and geochemical trappings. Geochemical trapping is considered as a storage mechanism, which can further increase storage capacity, effectiveness and security in terms of permanent CO2 sequestration. The injected CO2 can have geochemical interactions with pore fluid and reservoir rocks and transform into minerals. It is important to evaluate the capacity of reservoir rock for sequestrating CO2. In this study, sedimentary rock samples were collected from a 2-km-deep well in Midwestern Taiwan; and, the BCR sequential extraction experiments developed by European Union Measurement and Testing Programme were conducted. BCR was designed for extracting three major phases from soil, including exchangeable phase and carbonates (the first stage), reducible phase (the second stage) and oxidizable phase (the third stage). The chemistry of extracted solutions and rock residues were measured with ICP-MS and XRF, respectively. According to the results of XRF, considerable amounts of calcium and iron can be extracted by BCR procedures but other cations are negligible. In general, shale has a higher capacity of CO2 sequestration than sandstone. The first stage of extraction can release about 6 (sandstone) to 18.5 (shale) g of calcium from 1 kg rock, which are equivalent to 6.6 and 20.4 g CO2/kg rock, respectively. In the second stage extraction, 0.71 (sandstone) to 1.38 (shale) g/kg rock of iron can be released and can mineralized 0.56 to 1.08 g CO2/kg rock. However, there are no considerable cations extracted in the third stage of BCR as shown by the XRF analysis. In addition, the results of ICP-MS show that Mg can be released in the order of 10-3 g from 1 kg rock while cations of Zn, Co, Ni, Cd, Pb, Cu and Ba are in the order of 10-4 g.
Petrochemistry of Mafic Rocks Within the Northern Cache Creek Terrane, NW British Columbia, Canada

NASA Astrophysics Data System (ADS)

English, J. M.; Johnston, S. T.; Mihalynuk, M. G.

2002-12-01

The Cache Creek terrane is a belt of oceanic rocks that extend the length of the Cordillera in British Columbia. Fossil fauna in this belt are exotic with respect to the remainder of the Canadian Cordillera, as they are of equatorial Tethyan affinity, contrasting with coeval faunas in adjacent terranes that show closer linkages with ancestral North America. Preliminary results reported here from geochemical studies of mafic rocks within the Nakina area of NW British Columbia further constrain the origin of this enigmatic terrane. The terrane is typified by tectonically imbricated slices of chert, argillite, limestone, wacke and volcaniclastic rocks, as well as mafic and ultramafic rocks. These lithologies are believed to represent two separate lithotectonic elements: Upper Triassic to Lower Jurassic, subduction-related accretionary complexes, and dismembered basement assemblages emplaced during the closure of the Cache Creek ocean in the Middle Jurassic. Petrochemical analysis revealed four distinct mafic igneous assemblages that include: magmatic 'knockers' of the Nimbus serpentinite mélange, metabasalts of 'Blackcaps' Mountain, augite-phyric breccias of 'Laughing Moose' Creek, and volcanic pediments to the reef-forming carbonates of the Horsefeed Formation. Major and trace element analysis classifies the 'Laughing Moose' breccias and the carbonate-associated volcanics as alkaline in nature, whereas the rest are subalkaline. Tectonic discrimination diagrams show that the alkaline rocks are of within-plate affinity, while the 'Blackcaps' basalts and 'knockers' from within the mélange typically straddle the island-arc tholeiite and the mid-ocean ridge boundaries. However, primitive mantle normalized multi-element plots indicate that these subalkaline rocks have pronounced negative Nb anomalies, a characteristic arc signature. The spatial association of alkaline volcanic rocks with extensive carbonate domains points to the existence of seamounts within the Cache Creek ocean. However, the precise origin of the 'Laughing Moose' breccias remains somewhat uncertain and may be related to a subsequent rifting event. To conclude, preliminary data from the Nakina region show it to be dominated by two different petrogenetic components: alkaline volcanic rocks of within-plate affinity, and primitive arc-related, subalkaline mafic rocks. An accretionary complex/ oceanic arc origin may provide a mechanism to explain the lithological diversity within the Nakina area.
Context of Carbonate Rocks in Heavily Eroded Martian Terrain

NASA Technical Reports Server (NTRS)

2008-01-01

The color coding on this composite image of an area about 20 kilometers (12 miles) wide on Mars is based on infrared spectral information interpreted as evidence of various minerals present. Carbonate, which is indicative of a wet and non-acidic history, occurs in very small patches of exposed rock appearing green in this color representation, such as near the lower right corner.
The scene is heavily eroded terrain to the west of a small canyon in the Nili Fossae region of Mars. It was one of the first areas where researchers on the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) science team detected carbonate in Mars rocks. The spectral information comes from infrared imaging by CRISM, one of six science instruments on NASA's Mars Reconnaissance Orbiter. That coloring is overlaid on a grayscale image from the same orbiter's Context Camera.
The uppermost capping rock unit (purple) is underlain successively by banded olivine-bearing rocks (yellow) and rocks bearing iron-magnesium smectite clay (blue). Where the olivine is a greenish hue, it has been partially altered by interaction with water. The carbonate and olivine occupy the same level in the stratigraphy, and it is thought that the carbonate formed by aqueous alteration of olivine. The channel running from upper left to lower right through the image and eroding into the layers of bedrock testifies to the past presence of water in this region. That some of the channels are closely associated with carbonate (lower right) indicates that waters interacting with the carbonate were neutral to alkaline because acidic waters would have dissolved the carbonate.
Information for the color coding came from CRISM images catalogued as FRT0000B438, FRT0000A4FC, and FRT00003E12. This composite was made using 2.38-micrometer-wavelenghth data as red, 1.80 micrometer as green and 1.15 micrometer as blue.
The base black-and-white image, acquired at a resolution of 5 meters (16 feet) per pixel, is catalogued as CTX P03_002176_2024_XI_22N283W_070113 by the Context Camera science team.
NASA's Jet Propulsion Laboratory, a division of the California Institute of Technology, Pasadena, manages the Mars Reconnaissance Orbiter for the NASA Science Mission Directorate, Washington. Lockheed Martin Space Systems, Denver, is the prime contractor for the project and built the spacecraft. The Johns Hopkins University Applied Physics Laboratory led the effort to build the CRISM instrument and operates CRISM in coordination with an international team of researchers from universities, government and the private sector. Malin Space Science Systems, San Diego, provided and operates the Context Camera.
Geologic Map of the Shenandoah National Park Region, Virginia

USGS Publications Warehouse

Southworth, Scott; Aleinikoff, John N.; Bailey, Christopher M.; Burton, William C.; Crider, E.A.; Hackley, Paul C.; Smoot, Joseph P.; Tollo, Richard P.

2009-01-01

The geology of the Shenandoah National Park region of Virginia was studied from 1995 to 2008. The focus of the study was the park and surrounding areas to provide the National Park Service with modern geologic data for resource management. Additional geologic data of the adjacent areas are included to provide regional context. The geologic map can be used to support activities such as ecosystem delineation, land-use planning, soil mapping, groundwater availability and quality studies, aggregate resources assessment, and engineering and environmental studies. The study area is centered on the Shenandoah National Park, which is mostly situated in the western part of the Blue Ridge province. The map covers the central section and western limb of the Blue Ridge-South Mountain anticlinorium. The Skyline Drive and Appalachian National Scenic Trail straddle the drainage divide of the Blue Ridge highlands. Water drains northwestward to the South Fork of the Shenandoah River and southeastward to the James and Rappahannock Rivers. East of the park, the Blue Ridge is an area of low relief similar to the physiography of the Piedmont province. The Great Valley section of the Valley and Ridge province is west of Blue Ridge and consists of Page Valley and Massanutten Mountain. The distribution and types of surficial deposits and landforms closely correspond to the different physiographic provinces and their respective bedrock. The Shenandoah National Park is underlain by three general groups of rock units: (1) Mesoproterozoic granitic gneisses and granitoids, (2) Neoproterozoic metasedimentary rocks of the Swift Run Formation and metabasalt of the Catoctin Formation, and (3) siliciclastic rocks of the Lower Cambrian Chilhowee Group. The gneisses and granitoids mostly underlie the lowlands east of Blue Ridge but also rugged peaks like Old Rag Mountain (996 meter). Metabasalt underlies much of the highlands, like Stony Man (1,200 meters). The siliciclastic rocks underlie linear ridges from 800 to 400 meters in altitude. The Page Valley is underlain by Cambrian and Ordovician carbonate rocks. Siliciclastic rocks are mostly west of the South Fork of the Shenandoah River and underlie Massanutten Mountain. Surficial deposits in the highlands include colluvium and debris fans. The lowlands have broad alluvial fans, alluvial plains, and fluvial terraces. Ridges underlain by siliciclastic rocks have abundant boulder fields. Numerous sinkholes and caves are due to the dissolution of the carbonate bedrock.
Reactive transport modeling of the enhancement of density-driven CO 2 convective mixing in carbonate aquifers and its potential implication on geological carbon sequestration

DOE PAGES

Islam, Akand; Sun, Alexander Y.; Yang, Changbing

2016-04-20

We study the convection and mixing of CO 2 in a brine aquifer, where the spread of dissolved CO 2 is enhanced because of geochemical reactions with the host formations (calcite and dolomite), in addition to the extensively studied, buoyancy-driven mixing. The nonlinear convection is investigated under the assumptions of instantaneous chemical equilibrium, and that the dissipation of carbonate rocks solely depends on flow and transport and chemical speciation depends only on the equilibrium thermodynamics of the chemical system. The extent of convection is quantified in term of the CO 2 saturation volume of the storage formation. Our results suggestmore » that the density increase of resident species causes significant enhancement in CO 2 dissolution, although no significant porosity and permeability alterations are observed. Furthermore, early saturation of the reservoir can have negative impact on CO 2 sequestration.« less
Reactive Transport Modeling of the Enhancement of Density-Driven CO2 Convective Mixing in Carbonate Aquifers and its Potential Implication on Geological Carbon Sequestration.

PubMed

Islam, Akand; Sun, Alexander Y; Yang, Changbing

2016-04-20

We study the convection and mixing of CO2 in a brine aquifer, where the spread of dissolved CO2 is enhanced because of geochemical reactions with the host formations (calcite and dolomite), in addition to the extensively studied, buoyancy-driven mixing. The nonlinear convection is investigated under the assumptions of instantaneous chemical equilibrium, and that the dissipation of carbonate rocks solely depends on flow and transport and chemical speciation depends only on the equilibrium thermodynamics of the chemical system. The extent of convection is quantified in term of the CO2 saturation volume of the storage formation. Our results suggest that the density increase of resident species causes significant enhancement in CO2 dissolution, although no significant porosity and permeability alterations are observed. Early saturation of the reservoir can have negative impact on CO2 sequestration.
Source-rock geochemistry of the San Joaquin Basin Province, California: Chapter 11 in Petroleum systems and geologic assessment of oil and gas in the San Joaquin Basin Province, California

USGS Publications Warehouse

Peters, Kenneth E.; Magoon, Leslie B.; Valin, Zenon C.; Lillis, Paul G.

2007-01-01

Source-rock thickness and organic richness are important input parameters required for numerical modeling of the geohistory of petroleum systems. Present-day depth and thickness maps for the upper Miocene Monterey Formation, Eocene Tumey formation of Atwill (1935), Eocene Kreyenhagen Formation, and Cretaceous-Paleocene Moreno Formation source rocks in the San Joaquin Basin were determined using formation tops data from 266 wells. Rock-Eval pyrolysis and total organic carbon data (Rock-Eval/TOC) were collected for 1,505 rock samples from these source rocks in 70 wells. Averages of these data for each well penetration were used to construct contour plots of original total organic carbon (TOCo) and original hydrogen index (HIo) in the source rock prior to thermal maturation resulting from burial. Sufficient data were available to construct plots of TOCo and HIo for all source-rock units except the Tumey formation of Atwill (1935). Thick, organic-rich, oil-prone shales of the upper Miocene Monterey Formation occur in the Tejon depocenter in the southern part of the basin with somewhat less favorable occurrence in the Southern Buttonwillow depocenter to the north. Shales of the upper Miocene Monterey Formation generated most of the petroleum in the San Joaquin Basin. Thick, organic-rich, oil-prone Kreyenhagen Formation source rock occurs in the Buttonwillow depocenters, but it is thin or absent in the Tejon depocenter. Moreno Formation source rock is absent from the Tejon and Southern Buttonwillow depocenters, but thick, organic-rich, oil-prone Moreno Formation source rock occurs northwest of the Northern Buttonwillow depocenter adjacent to the southern edge of Coalinga field.

Numerical modelling of fault reactivation in carbonate rocks under fluid depletion conditions - 2D generic models with a small isolated fault

NASA Astrophysics Data System (ADS)

Zhang, Yanhua; Clennell, Michael B.; Delle Piane, Claudio; Ahmed, Shakil; Sarout, Joel

2016-12-01

This generic 2D elastic-plastic modelling investigated the reactivation of a small isolated and critically-stressed fault in carbonate rocks at a reservoir depth level for fluid depletion and normal-faulting stress conditions. The model properties and boundary conditions are based on field and laboratory experimental data from a carbonate reservoir. The results show that a pore pressure perturbation of -25 MPa by depletion can lead to the reactivation of the fault and parts of the surrounding damage zones, producing normal-faulting downthrows and strain localization. The mechanism triggering fault reactivation in a carbonate field is the increase of shear stresses with pore-pressure reduction, due to the decrease of the absolute horizontal stress, which leads to an expanded Mohr's circle and mechanical failure, consistent with the predictions of previous poroelastic models. Two scenarios for fault and damage-zone permeability development are explored: (1) large permeability enhancement of a sealing fault upon reactivation, and (2) fault and damage zone permeability development governed by effective mean stress. In the first scenario, the fault becomes highly permeable to across- and along-fault fluid transport, removing local pore pressure highs/lows arising from the presence of the initially sealing fault. In the second scenario, reactivation induces small permeability enhancement in the fault and parts of damage zones, followed by small post-reactivation permeability reduction. Such permeability changes do not appear to change the original flow capacity of the fault or modify the fluid flow velocity fields dramatically.
Simulation of geochemical processes responsible for the formation of the Zhezqazghan deposit

NASA Astrophysics Data System (ADS)

Ryzhenko, B. N.; Cherkasova, E. V.

2014-05-01

Physicochemical computer simulation of water-rock systems at a temperature of 25-150°C and under a pressure of up to 600 bar has been carried out for quantitative description of the mineralization formation conditions at sandstone- and shale-hosted copper deposits. The simulation is based on geological and geochemical information concerning the Zhezqazghan deposit and considers (i) a source of ore matter, (ii) composition of the fluid that transfers ore matter to the ore formation zone, and (iii) factors of ore concentration. It has been shown that extraction of copper from minerals of rocks and its accumulation in aqueous solution are optimal at a high mass ratio of rock to water (R/W > 10), Eh of +200 to -100 mV, and an obligatory content of chloride ions in the aqueous phase. The averaged ore-bearing fluid Cl95SO44//Ca50(Na + K)30Mg19 (eq %), pH ˜ 4, mineralization of up to 400 g/L, is formed by the interaction of red sandstone beds with a sedimentogenic brine (a product of metamorphism of seawater in carbonate rocks enriched in organic matter). The ore concentration proceeds in the course of cooling from 150 to 50°C during filtration of ore-bearing fluid through red sandstone beds in the rock-water system thermodynamically opened with respect to the reductive components.
Geochemical processes leading to the precipitation of subglacial carbonate crusts at Bossons glacier, Mont Blanc Massif (French Alps)

NASA Astrophysics Data System (ADS)

Thomazo, Christophe; Buoncristiani, Jean-Francois; Vennin, Emmanuelle; Pellenard, Pierre; Cocquerez, Theophile; Mugnier, Jean L.; Gérard, Emmanuelle

2017-09-01

Cold climate carbonates can be used as paleoclimatic proxies. The mineralogy and isotopic composition of subglacially precipitated carbonate crusts provide insights into the subglacial conditions and processes occurring at the meltwater-basement rock interface of glaciers. This study documents such crusts discovered on the lee side of a gneissic roche moutonnée at the terminus of the Bossons glacier in the Mont Blanc Massif area (France). The geological context and mineralogical investigations suggest that the Ca used for the precipitation of large crystals of radial fibrous sparite observed in these crusts originated from subglacial chemical weathering of Ca-bearing minerals of the local bedrock (plagioclase and amphibole). Measurements of the carbon and oxygen isotope compositions in the crusts indicate precipitation at, or near to, equilibrium with the basal meltwater under open system conditions during refreezing processes. The homogeneous and low carbonate δ13C values (ca. -11.3‰) imply a large contribution of soil organic carbon to the Bossons subglacial meltwater carbon reservoir at the time of deposition. In addition, organic remains trapped within the subglacially precipitated carbonate crusts give an age of deposition around 6500 years cal BP suggesting that the Mid-Holocene climatic and pedological optima are archived in the Bossons glacier carbonate crusts.
VNIR reflectance spectroscopy of natural carbonate rocks: implication for remote sensing identification of fault damage zones

NASA Astrophysics Data System (ADS)

Traforti, Anna; Mari, Giovanna; Carli, Cristian; Demurtas, Matteo; Massironi, Matteo; Di Toro, Giulio

2017-04-01

Reflectance spectroscopy in the visible and near-infrared (VNIR) is a common technique used to study the mineral composition of Solar System bodies from remote sensed and in-situ robotic exploration. In the VNIR spectral range, both crystal field and vibrational overtone absorptions can be present with spectral characteristics (i.e. albedo, slopes, absorption band with different positions and depths) that vary depending on composition and texture (e.g. grain size, roughness) of the sensed materials. The characterization of the spectral variability related to the rock texture, especially in terms of grain size (i.e., both the size of rock components and the size of particulates), commonly allows to obtain a wide range of information about the different geological processes modifying the planetary surfaces. This work is aimed at characterizing how the grain size reduction associated to fault zone development produces reflectance variations in rock and mineral spectral signatures. To achieve this goal we present VNIR reflectance analysis of a set of fifteen rock samples collected at increasing distances from the fault core of the Vado di Corno fault zone (Campo Imperatore Fault System - Italian Central Apennines). The selected samples had similar content of calcite and dolomite but different grain size (X-Ray Powder Diffraction, optical and scanning electron microscopes analysis). Consequently, differences in the spectral signature of the fault rocks should not be ascribed to mineralogical composition. For each sample, bidirectional reflectance spectra were acquired with a Field-Pro Spectrometer mounted on a goniometer, on crushed rock slabs reduced to grain size <800, <200, <63, <10 μm and on intact fault zone rock slabs. The spectra were acquired on dry samples, at room temperature and normal atmospheric pressure. The source used was a Tungsten Halogen lamp with an illuminated spot area of ca. 0.5 cm2and incidence and emission angles of 30˚ and 0˚ respectively. The spectral analysis of the crushed and intact rock slabs in the VNIR spectral range revealed that in both cases, with increasing grain size: (i) the reflectance decreases (ii) VNIR spectrum slopes (i.e. calculated between wavelengths of 0.425 - 0.605 μm and 2.205 - 2.33 μm, respectively) and (iii) carbonate main absorption band depth (i.e. vibrational absorption band at wavelength of ˜2.3 μm) increase. In conclusion, grain size variations resulting from the fault zone evolution (e.g., cumulated slip or development of thick damage zones) produce reflectance variations in rocks and mineral spectral signatures. The remote sensing analysis in the VNIR spectral range can be applied to identify the spatial distribution and extent of fault core and damage zone domains for industrial and seismic hazard applications. Moreover, the spectral characterization of carbonate-built rocks can be of great interest for the surface investigation of inner planets (e.g. Earth and Mars) and outer bodies (e.g. Galilean icy satellites). On these surfaces, carbonate minerals at different grain sizes are common and usually related to water and carbon distribution, with direct implications for potential life outside Earth (e.g. Mars).
Potential and costs of carbon dioxide removal by enhanced weathering of rocks

NASA Astrophysics Data System (ADS)

Strefler, Jessica; Amann, Thorben; Bauer, Nico; Kriegler, Elmar; Hartmann, Jens

2018-03-01

The chemical weathering of rocks currently absorbs about 1.1 Gt CO2 a-1 being mainly stored as bicarbonate in the ocean. An enhancement of this slow natural process could remove substantial amounts of CO2 from the atmosphere, aiming to offset some unavoidable anthropogenic emissions in order to comply with the Paris Agreement, while at the same time it may decrease ocean acidification. We provide the first comprehensive assessment of economic costs, energy requirements, technical parameterization, and global and regional carbon removal potential. The crucial parameters defining this potential are the grain size and weathering rates. The main uncertainties about the potential relate to weathering rates and rock mass that can be integrated into the soil. The discussed results do not specifically address the enhancement of weathering through microbial processes, feedback of geogenic nutrient release, and bioturbation. We do not only assess dunite rock, predominantly bearing olivine (in the form of forsterite) as the mineral that has been previously proposed to be best suited for carbon removal, but focus also on basaltic rock to minimize potential negative side effects. Our results show that enhanced weathering is an option for carbon dioxide removal that could be competitive already at 60 US t-1 CO2 removed for dunite, but only at 200 US t-1 CO2 removed for basalt. The potential carbon removal on cropland areas could be as large as 95 Gt CO2 a-1 for dunite and 4.9 Gt CO2 a-1 for basalt. The best suited locations are warm and humid areas, particularly in India, Brazil, South-East Asia and China, where almost 75% of the global potential can be realized. This work presents a techno-economic assessment framework, which also allows for the incorporation of further processes.
Multi-scale Pore Imaging Techniques to Characterise Heterogeneity Effects on Flow in Carbonate Rock

NASA Astrophysics Data System (ADS)

Shah, S. M.

2017-12-01

Digital rock analysis and pore-scale studies have become an essential tool in the oil and gas industry to understand and predict the petrophysical and multiphase flow properties for the assessment and exploitation of hydrocarbon reserves. Carbonate reservoirs, accounting for majority of the world's hydrocarbon reserves, are well known for their heterogeneity and multiscale pore characteristics. The pore sizes in carbonate rock can vary over orders of magnitudes, the geometry and topology parameters of pores at different scales have a great impact on flow properties. A pore-scale study is often comprised of two key procedures: 3D pore-scale imaging and numerical modelling techniques. The fundamental problem in pore-scale imaging and modelling is how to represent and model the different range of scales encountered in porous media, from the pore-scale to macroscopic petrophysical and multiphase flow properties. However, due to the restrictions of image size vs. resolution, the desired detail is rarely captured at the relevant length scales using any single imaging technique. Similarly, direct simulations of transport properties in heterogeneous rocks with broad pore size distributions are prohibitively expensive computationally. In this study, we present the advances and review the practical limitation of different imaging techniques varying from core-scale (1mm) using Medical Computed Tomography (CT) to pore-scale (10nm - 50µm) using Micro-CT, Confocal Laser Scanning Microscopy (CLSM) and Focussed Ion Beam (FIB) to characterise the complex pore structure in Ketton carbonate rock. The effect of pore structure and connectivity on the flow properties is investigated using the obtained pore scale images of Ketton carbonate using Pore Network and Lattice-Boltzmann simulation methods in comparison with experimental data. We also shed new light on the existence and size of the Representative Element of Volume (REV) capturing the different scales of heterogeneity from the pore-scale imaging.
Hydraulic seals and their origin: Evidence from the stable isotope geochemistry of dolomites in the Middle Ordovician St. Peter Sandstone, Michigan basin

DOE Office of Scientific and Technical Information (OSTI.GOV)

Winter, B.L.; Johnson, C.M.; Valley, J.W.

1995-01-01

Regionally extensive, overpressured natural gas pools within the St. Peter Sandstone (Middle Ordovician) of the Michigan basin are bounded by rock types that include 3-7-m-thick zones of low-permeability, low-porosity carbonates or diagenetically banded quartz sandstones. Replacive dolomite from an approximately 5-m-thick carbonate interval in the east-central portion of the Michigan basin has very low {delta}{sup 13}C values that systematically decrease from approximately -5% at the top to -10% (PDB) at the base. {delta}{sup 18}O values for the replacive dolomite also decrease systematically with depth from approximately 27 to 23% (SMOW). These data suggest an upward decrease in isotope exchange betweenmore » the replacive dolomitization fluid and the precursors rock (i.e., the system was rock dominated at the top of the carbonate interval), which implies upward, cross-formational movement of the dolomitizing fluid. Fluid-rock interaction modeling suggest that the dolomitizing fluid had a total dissolved carbon (TDC) content of approximately 4000 ppm and a {delta}{sup 13}C value of -27%, which indicates that the carbon was primarily derived from organic diagenesis. Sr isotope and major element data suggest that this dolomitizing fluid had a modified seawater origin. The {delta}{sup 13}C values of sandstone intervals from three locations in the central portion of the Michigan basin range from -9 to -4% and are relatively invariant at a particular locality; therefore, the TDC of the dolomitizing fluid in the central Michigan basin is interpreted to have contained only about 20-30% organic carbon. The fact that all dolomites analyzed in the St. Peter Sandstone have much lower {Delta}{sup 13}C values that carbonates in adjacent formations indicates that dolomitization and the formation of hydraulic seals were related to organic matter diagenesis.« less
Imaging of karsts on buried carbonate platform in Central Luconia Province, Malaysia

NASA Astrophysics Data System (ADS)

Nur Fathiyah Jamaludin, Siti; Mubin, Mukhriz; Latiff, Abdul Halim Abdul

2017-10-01

Imaging of carbonate rocks in the subsurface through seismic method is always challenging due to its heterogeneity and fast velocity compared to the other rock types. Existence of karsts features on the carbonate rocks make it more complicated to interpret the reflectors. Utilization of modern interpretation software such as PETREL and GeoTeric® to image the karsts morphology make it possible to model the karst network within the buried carbonate platform used in this study. Using combination of different seismic attributes such as Variance, Conformance, Continuity, Amplitude, Frequency and Edge attributes, we are able to image the karsts features that are available in the proven gas-field in Central Luconia Province, Malaysia. The mentioned attributes are excellent in visualize and image the stratigraphic features based on the difference in their acoustic impedance as well as structural features, which include karst. 2D & 3D Karst Models were developed to give a better understanding on the characteristics of the identified karsts. From the models, it is found that the karsts are concentrated in the top part of the carbonate reservoir (epikarst) and the middle layer with some of them becomes extensive and create karst networks, either laterally or vertically. Most of the vertical network karst are related to the existence of faults that displaced all the horizons in the carbonate platform.
Radium isotope quartet in groundwater as a proxy for identification of aquifer rocks and mechanisms of water-rock interactions: examples from the Negev, Israel

NASA Astrophysics Data System (ADS)

Vengosh, A.; Pery, N.; Paytan, A.; Haquin, G.; Elhanani, S.; Pankratov, I.

2006-05-01

Many aquifer systems are composed of multiple rock types. Previous attempts to evaluate the specific aquifer rocks that control the groundwater chemistry and possible flow paths within these multiple lithological systems have used major ion chemistry and isotopic tracers (e.g., strontium isotopes). Here we propose an additional isotopic proxy that is based on the distribution of radium isotopes in groundwater. Radium has four radioactive isotopes that are part of the decay chains of uranium-238, thorium-232, and uranium-235. The abundance of radium isotope quartet (226Ra-half life 1600 y; 228Ra-5.6 y; 224Ra-3.6 d; 223Ra-11.4 d) in groundwater reflects the Th/U ratios in the rocks. Investigation of groundwater from the Negev, Israel, enabled us to discriminate between groundwaters flowing in the Lower Cretaceous Nubian Sandstone and the Upper Cretaceous Judea Group carbonate aquifers. Groundwater flowing in the sandstone aquifer has distinguishably high 228Ra/226Ra and 224Ra/223Ra ratios due to the high Th/U ratio in sandstone. In contrast, the predominance of uranium in carbonate rocks results in low 228Ra/226Ra and 224Ra/223Ra ratios in the associated groundwater. We show that the radium activity in groundwater in the two-aquifer systems is correlated with temperature, dissolved oxygen, and salinity. The increase of radium activity is also associated with changes in the isotopic ratios; 228Ra/226Ra ratios increase and decrease in the sandstone and carbonate aquifers, respectively. Given that the dissolution of radium isotopes depends on their decay constants, the use of the four radium isotopes with different decay constants enabled us to distinguish between dissolution (higher abundance of the long-lived isotopes) and recoil (predominance of the short-lived isotopes) processes. In spite of these isotopic fractionations, the radium isotopic discrimination between carbonate and sandstone aquifers is significant.
The Impact of the Flow Field Heterogeneity and of the Injection Rate on the Effective Reaction Rates in Carbonates: a Study at the Pore Scale

NASA Astrophysics Data System (ADS)

Nunes, J. P. P.; Bijeljic, B.; Blunt, M. J.

2015-12-01

Carbonate rocks are notoriously difficult to characterize. Their abrupt facies variations give rise to drastic changes in the petrophysical properties of the reservoir. Such heterogeneity, when further associated with variations in rock mineralogy due to diagenetic processes, result in a challenging scenario to model from the pore to the field scale. Micro-CT imaging is one of the most promising technologies to characterize porous rocks. The understanding at the pore scale of reactive and non-reactive transport is being pushed forward by recent developments in both imaging capability - 3D images with resolution of a few microns - and in modeling techniques - flow simulations in giga-cell models. We will present a particle-based method capable of predicting the evolution of petrophysical properties of carbonate cores subjected to CO2 injection at reservoir conditions (i.e. high pressures and temperatures). Reactive flow is simulated directly on the voxels of high resolution micro-CT images of rocks. Reactants are tracked using a semi-analytical streamline tracing algorithm and rock-fluid interaction is controlled by the diffusive flux of particles from the pores to the grains. We study the impact of the flow field heterogeneity and of the injection rate on the sample-averaged (i.e. effective) reaction rate of calcite dissolution in three rocks of increasing complexity: a beadpack, an oolitic limestone and a bioclastic limestone. We show how decreases in the overall dissolution rate depend on both the complexity of the pore space and also on the flow rate. This occurs even in chemically homogenous rocks. Our results suggest that the large differences observed between laboratory and field scale rates could, in part, be explained by the inhomogeneity in the flow field at the pore scale and the consequent transport-limited flux of reactants at the solid surface. Our results give valuable insight into the processes governing carbonate dissolution and provide a starting point to the refinement of upscaling techniques for reactive flows. Potential impacts for reservoir development and monitoring will also be discussed.
Rock magnetic signature of paleoenvironmental changes in the Izu Bonin rear arc over the last 1 Ma

NASA Astrophysics Data System (ADS)

Kars, Myriam; Vautravers, Maryline; Musgrave, Robert; Kodama, Kazuto

2015-04-01

During April and May 2014, IODP Expedition 350 drilled a 1806.5 m deep hole at Site U1437 in the Izu-Bonin rear arc, in order to understand, among other objectives, the compositional evolution of the arc since the Miocene and track the missing half of the subduction factory. The good recovery of mostly fine grained sediments at this site enables a high resolution paleontological and rock magnetic studies. Particularly, variations in magnetic properties and mineralogy are well documented. Natural remanent magnetization and magnetic susceptibility vary with a saw-tooth pattern. Routine rock magnetic measurements performed on about 400 samples in the first 120 meters of Hole U1437B showed that pseudo single domain to multidomain magnetite is the main carrier of the remanence. The origin of magnetite is likely detrital. The magnetic susceptibility variations depend on many factors (e.g. lithology, magnetic mineralogy, and also dilution by the carbonate matrix). The magnetic susceptibility is also used as a proxy, at first order, for magnetic minerals concentration. In order to highlight changes in magnetic minerals concentration, it's necessary to correct for the carbonate dilution effect. Onboard and onshore carbonate measurements by coulometry show that the carbonate content of the samples can be up to ~60%. About 70 samples were measured onshore. After correcting the susceptibility by the carbonate content measured on the same samples, it appears that the pattern of the magnetic susceptibility before and after correction is similar. Then the magnetic susceptibility variations do not result from carbonate dilution but reflect fluctuating influx of the detrital sediment component. The delta O18 variations obtained on foraminifers (N. dutertrei) show MIS 1 to MIS 25 over the studied interval covering the last 1 Ma (see Vautravers et al., this meeting). Rock magnetic properties, concentration and grain size variations of the magnetic minerals will be compared to climatic proxies in order to investigate the rock magnetic signature of climate changes in the Izu Bonin rear arc in the Late Pleistocene.
Alteration of fault rocks by CO2-bearing fluids with implications for sequestration

NASA Astrophysics Data System (ADS)

Luetkemeyer, P. B.; Kirschner, D. L.; Solum, J. G.; Naruk, S.

2011-12-01

Carbonates and sulfates commonly occur as primary (diagenetic) pore cements and secondary fluid-mobilized veins within fault zones. Stable isotope analyses of calcite, formation fluid, and fault zone fluids can help elucidate the carbon sources and the extent of fluid-rock interaction within a particular reservoir. Introduction of CO2 bearing fluids into a reservoir/fault system can profoundly affect the overall fluid chemistry of the reservoir/fault system and may lead to the enhancement or degradation of porosity within the fault zone. The extent of precipitation and/or dissolution of minerals within a fault zone can ultimately influence the sealing properties of a fault. The Colorado Plateau contains a number of large carbon dioxide reservoirs some of which leak and some of which do not. Several normal faults within the Paradox Basin (SE Utah) dissect the Green River anticline giving rise to a series of footwall reservoirs with fault-dependent columns. Numerous CO2-charged springs and geysers are associated with these faults. This study seeks to identify regional sources and subsurface migration of CO2 to these reservoirs and the effect(s) faults have on trap performance. Data provided in this study include mineralogical, elemental, and stable isotope data for fault rocks, host rocks, and carbonate veins that come from two localities along one fault that locally sealed CO2. This fault is just tens of meters away from another normal fault that has leaked CO2-charged waters to the land surface for thousands of years. These analyses have been used to determine the source of carbon isotopes from sedimentary derived carbon and deeply sourced CO2. XRF and XRD data taken from several transects across the normal faults are consistent with mechanical mixing and fluid-assisted mass transfer processes within the fault zone. δ13C range from -6% to +10% (PDB); δ18O values range from +15% to +24% (VSMOW). Geochemical modeling software is used to model the alteration productions of fault rocks from fluids of various chemistries coming from several different reservoirs within an active CO2-charged fault system. These results are compared to data obtained in the field.
Enhanced oxidative weathering in glaciated mountain catchments: A stabilising feedback on atmospheric carbon dioxide?

NASA Astrophysics Data System (ADS)

Horan, K.; Hilton, R. G.; Burton, K. W.; Selby, D. S.; Ottley, C. J.

2015-12-01

Mountain belts act as sources of carbon dioxide (CO2) to the atmosphere if physical erosion and exhumation expose rock-derived organic carbon ('petrogenic' organic carbon, OCpetro) to chemical weathering. Estimates suggest 15x1021g of carbon is stored in rocks globally as OCpetro, ~25,000 times the amount of carbon in the pre-industrial atmosphere. Alongside volcanic and metamorphic degassing, OCpetro weathering is thought to be the main source of CO2 to the atmosphere over geological timescales. Erosion in mountain river catchments has been shown to enhance oxidative weathering and CO2 release. However, we still lack studies which quantify this process. In addition, it is not clear how glaciation may impact OCpetro oxidation. In analogy with silicate weathering, large amounts of fine sediment in glacial catchments may enhance oxidative weathering. Here we quantify oxidative weathering in nine catchments draining OCpetro bearing rocks in the western Southern Alps, New Zealand. Using rhenium (Re) as a tracer of oxidative weathering, we develop techniques to precisely measure Re concentration at sub-ppt levels in river waters. Using [Re]water/[Re]rock as a weathering tracer, we estimate that the weathering efficiency in glacial catchments is >4 times that of non-glacial catchments. Combining this with the OCpetro content of rocks and dissolved Re flux, we estimate the CO2 release by OCpetro oxidation. The analysis suggests that non-glacial catchments in the western Southern Alps release similar amounts of CO2 as catchments in Taiwan where erosion rates are comparable. In this mountain belt, the CO2 release does not negate CO2 drawdown by silicate weathering and by riverine transfer of organic matter. Based on our results, we propose that mountain glaciation may greatly enhance OCpetro oxidation rates. Depending on the global fluxes involved, this provides a feedback to damp low atmospheric CO2 levels and global cooling. During glacial periods (low CO2, low global temperatures), increased CO2 emissions by OCpetro oxidation in mountain belts may act to counter global cooling.
40 CFR Table Z-1 to Subpart Z of... - Default Chemical Composition of Phosphate Rock by Origin

Code of Federal Regulations, 2013 CFR

2013-07-01

... 40 Protection of Environment 22 2013-07-01 2013-07-01 false Default Chemical Composition of Phosphate Rock by Origin Z Table Z-1 to Subpart Z of Part 98 Protection of Environment ENVIRONMENTAL... Phosphate Rock by Origin Origin Total carbon(percent by weight) Central Florida 1.6 North Florida 1.76 North...
40 CFR Table Z-1 to Subpart Z of... - Default Chemical Composition of Phosphate Rock by Origin

Code of Federal Regulations, 2012 CFR

2012-07-01

... 40 Protection of Environment 22 2012-07-01 2012-07-01 false Default Chemical Composition of Phosphate Rock by Origin Z Table Z-1 to Subpart Z of Part 98 Protection of Environment ENVIRONMENTAL... Phosphate Rock by Origin Origin Total carbon(percent by weight) Central Florida 1.6 North Florida 1.76 North...
40 CFR Table Z-1 to Subpart Z of... - Default Chemical Composition of Phosphate Rock by Origin

Code of Federal Regulations, 2014 CFR

2014-07-01

... 40 Protection of Environment 21 2014-07-01 2014-07-01 false Default Chemical Composition of Phosphate Rock by Origin Z Table Z-1 to Subpart Z of Part 98 Protection of Environment ENVIRONMENTAL... Phosphate Rock by Origin Origin Total carbon(percent by weight) Central Florida 1.6 North Florida 1.76 North...
40 CFR Table Z-1 to Subpart Z of... - Default Chemical Composition of Phosphate Rock by Origin

Code of Federal Regulations, 2011 CFR

2011-07-01

... 40 Protection of Environment 21 2011-07-01 2011-07-01 false Default Chemical Composition of Phosphate Rock by Origin Z Table Z-1 to Subpart Z of Part 98 Protection of Environment ENVIRONMENTAL... Phosphate Rock by Origin Origin Total carbon(percent by weight) Central Florida 1.6 North Florida 1.76 North...
Lithogeochemical character of near-surface bedrock in the New England coastal basins

USGS Publications Warehouse

Robinson, Gilpin R.; Ayotte, Joseph D.; Montgomery, Denise L.; DeSimone, Leslie A.

2002-01-01

This geographic information system (GIS) data layer shows the generalized lithologic and geochemical, termed lithogeochemical, character of near-surface bedrock in the New England Coastal Basin (NECB) study area of the U.S. Geological Survey's National Water Quality Assessment (NAWQA) Program. The area encompasses 23,000 square miles in western and central Maine, eastern Massachusetts, most of Rhode Island, eastern New Hampshire and a small part of eastern Connecticut. The NECB study area includes the Kennebec, Androscoggin, Saco, Merrimack, Charles, and Blackstone River Basins, as well as all of Cape Cod. Bedrock units in the NECB study area are classified into lithogeochemical units based on the relative reactivity of their constituent minerals to dissolution and the presence of carbonate or sulfide minerals. The 38 lithogeochemical units are generalized into 7 major groups: (1) carbonate-bearing metasedimentary rocks; (2) primarily noncalcareous, clastic sedimentary rocks with restricted deposition in discrete fault-bounded sedimentary basins of Mississipian or younger age; (3) primarily noncalcareous, clastic sedimentary rocks at or above biotite-grade of regional metamorphism; (4) mafic igneous rocks and their metamorphic equivalents; (5) ultramafic rocks; (6) felsic igneous rocks and their metamorphic equivalents; and (7) unconsolidated and poorly consolidated sediments.
Preservation of overmature, ancient, sedimentary organic matter in carbonate concretions during outcrop weathering.

PubMed

Loyd, S J

2017-01-01

Concretions are preferentially cemented zones within sediments and sedimentary rocks. Cementation can result from relatively early diagenetic processes that include degradation of sedimentary organic compounds or methane as indicated by significantly 13 C-depleted or enriched carbon isotope compositions. As minerals fill pore space, reduced permeability may promote preservation of sediment components from degradation during subsequent diagenesis, burial heating and outcrop weathering. Discrete and macroscopic organic remains, macro and microfossils, magnetic grains, and sedimentary structures can be preferentially preserved within concretions. Here, Cretaceous carbonate concretions of the Holz Shale are shown to contain relatively high carbonate-free total organic carbon (TOC) contents (up to ~18.5 wt%) compared to the surrounding host rock (with <2.1 wt%). TOC increases with total inorganic carbon (TIC) content, a metric of the degree of cementation. Pyrite contents within concretions generally correlate with organic carbon contents. Concretion carbonate carbon isotope compositions (δ 13 C carb ) range from -22.5 to -3.4‰ (VPDB) and do not correlate strongly with TOC. Organic carbon isotope compositions (δ 13 C org ) of concretions and host rock are similar. Thermal maturity data indicate that both host and concretion organic matter are overmature and have evolved beyond the oil window maturity stage. Although the organic matter in general has experienced significant oxidative weathering, concretion interiors exhibit lower oxygen indices relative to the host. These results suggest that carbonate concretions can preferentially preserve overmature, ancient, sedimentary organic matter during outcrop weathering, despite evidence for organic matter degradation genetic mechanisms. As a result, concretions may provide an optimal proxy target for characterization of more primary organic carbon concentrations and chemical compositions. In addition, these findings indicate that concretions can promote delayed oxidative weathering of organic carbon in outcrop and therefore impact local chemical cycling. © 2016 John Wiley & Sons Ltd.
Chemical effects of carbon dioxide sequestration in the Upper Morrow Sandstone in the Farnsworth, Texas, hydrocarbon unit

DOE Office of Scientific and Technical Information (OSTI.GOV)

Ahmmed, Bulbul; Appold, Martin S.; Fan, Tianguang

Numerical geochemical modeling was used to study the effects on pore-water composition and mineralogy from carbon dioxide (CO2) injection into the Pennsylvanian Morrow B Sandstone in the Farnsworth Unit in northern Texas to evaluate its potential for long-term CO2 sequestration. Speciation modeling showed the present Morrow B formation water to be supersaturated with respect to an assemblage of zeolite, clay, carbonate, mica, and aluminum hydroxide minerals and quartz. The principal accessory minerals in the Morrow B, feldspars and chlorite, were predicted to dissolve. A reaction-path model in which CO2 was progressively added up to its solubility limit into the Morrowmore » B formation water showed a decrease in pH from its initial value of 7 to approximately 4.1 to 4.2, accompanied by the precipitation of small amounts of quartz, diaspore, and witherite. As the resultant CO2-charged fluid reacted with more of the Morrow B mineral matrix, the model predicted a rise in pH, reaching a maximum of 5.1 to 5.2 at a water–rock ratio of 10:1. At a higher water–rock ratio of 100:1, the pH rose to only 4.6 to 4.7. Diaspore, quartz, and nontronite precipitated consistently regardless of the water–rock ratio, but the carbonate minerals siderite, witherite, dolomite, and calcite precipitated at higher pH values only. As a result, CO2 sequestration by mineral trapping was predicted to be important only at low water–rock ratios, accounting for a maximum of 2% of the added CO2 at the lowest water–rock ratio investigated of 10:1, which corresponds to a small porosity increase of approximately 0.14% to 0.15%.« less

Performance and Characterization of Shear Ties for Use in Insulated Precast Concrete Sandwich Wall Panels

DTIC Science & Technology

2010-11-01

stainless 14 steel, galvanized carbon steel, carbon- fiber -reinforced polymer (CFRP), glass- fiber -reinforced polymer 15 (GFRP), and basalt - fiber ...CFRP Grid, (E) Universal Building Products GFRP Teplo Tie, and (F) Universal Building Products 6 Basalt FRP RockBar. Traditional steel connections...1.6 E Universal Building Products TeploTie GFRP Tie 10 mm dia. x 150 mm F RockBar Basalt FRP Bar 7 in. x 5/16 in. G TSA Manufacturing C-Clip
Investigation of Reactions between Glauconite and Carbon Dioxide, with Implications for Carbon Sequestration

NASA Astrophysics Data System (ADS)

Nguyen, A. V.; Gabitov, R. I.; Beckingham, L. E.; Toghiani, H.; Fei, Y.; Kirkland, B. L.

2017-12-01

Mineral trapping is one potentially effective technology for long-term storage of carbon dioxide in a subsurface environment that has high temperature and pressure. Conceptually, upon injection of CO2 as a supercritical fluid into geological formations, the CO2 will react with the host rock to form a secondary carbonate mineral that is stable, thus creating a long-term carbon sink under thermodynamic condition of the reaction. Previous studies have demonstrated crystallization of magnesite by reactivity of CO2 and olivine-bearing basalt. Glauconite, a Fe/Ca/Mg bearing aluminosilicate mineral, a potential candidate for reaction with CO2 is common in sedimentary rock formations. The objectives of this study are to 1) develop a protocol for testing mineral trapping in the subsurface and 2) use that protocol to test the reactivity and effectiveness of the mineral glauconite in carbon sequestration. A sample from the Cambrian Riley Formation of Central Texas was selected for this study because it is extremely rich in glauconite. Mineral composition of the powdered sample was investigated by X-ray diffraction (XRD), which revealed that the glauconitic sandstone contains glauconite 20.4%, quartz 71%, and celadonite 8.6%. In the first experiment, 1.5 g of 0.01- 0.5 cm diameter grains reacted with a supercritical CO2 fluid in 30 g of sea water. The laboratory experiment was conducted in a stainless steel vessel in situ reservoir conditions at 120 degrees Celsius and 100 bars. After CO2 injection, pH of the brine decreased from 8.23 to 7. Scanning electron microscopy (SEM) and X-ray diffraction method showed no carbonate formed after 10 days of reaction. However, further experimental modifications facilitated formation of calcite at higher pH. In the second experiment, 0.7 g of 10-75 μm grains presumably reacted with CO2 formed by ammonium carbonate decomposition in a brine of NaCl 0.5 and CaCl2 0.25M; pH after the end of experiment was 7.74. The autoclave was set at 120 degrees Celsius and pressure of saturated water vapour for 14 days. XRD and EDS confirmed the presence of calcite in the sample after the treatment. This material is based upon work supported by the Department of Energy National Energy Technology Laboratory under the Southern States Energy Board's Cooperative Agreement Award Number DE-FE0029465.
Effects of fluids on rock deformation and fault slip: From nature to societal impact (Louis Néel Medal Lecture)

NASA Astrophysics Data System (ADS)

Spiers, Christopher J.

2017-04-01

Understanding the effects of fluid-rock interaction on rock and fault mechanical behaviour is central not only to understanding natural tectonic and seismogenic processes, and phenomena such as resource trapping, but also to evaluating the impact of industrial operations in the Earth's crust. These include activities ranging from extraction of geo-energy to geological storage of fuels, CO2 and wastes. For the assessment of both natural and induced geohazards, a physics-based approach to quantifying rock mechanical behaviour is unmissable. Microstructural studies of rocks deformed naturally in the mid and upper crust, or at seismogenic depths in subduction zones, show widespread evidence for brittle deformation (cataclasis), dissolution-precipitation transfer, fluid-related reactions producing weak minerals, and dilatation/cementation of fractures, cracks and pores. In addition, experimental work on rocks and simulated fault gouges has shown that the presence of water strongly influences their mechanical and transport properties. This implies the operation of fluid-assisted deformation mechanisms, such as stress corrosion cracking and diffusive mass transfer (pressure solution). More recently, other fluid-coupled deformation processes have been recognised, in rocks from peridotites and granites to sandstones, limestones and shales. In this lecture, I will give an overview of progress in this area. I will address the physics of pressure solution and stress corrosion cracking and how they contribute to the deformation and compaction of sandstone, carbonate and evaporite rocks in the mid and upper crust, under natural conditions and in the context of deformation caused by geo-resources production and geo-storage. New results on how these processes are affected by pore fluid salinity, gas content and CO2 activity will also be considered, as will data on the effects of mineral-fluid reactions and associated volume changes on rock deformation, fracturing and transport. The effects of gas and CO2 sorption on the stress-strain behaviour and permeability of clay and shale caprocks, recently reported in relation to seal integrity, will be addressed too, and compared with similar phenomena familiar in seen in coal seams. Lastly, I will address the effects of fluid-rock interaction on the frictional behaviour of faults. Recent low velocity friction experiments (<100 μm/s) performed on simulated carbonate, evaporite and quartz gouges, with varying phyllosilicate content, indicate that pressure solution is key to determining whether frictional slip is velocity-strengthening (stable) or velocity weakening (potentially seismogenic). An important trend seen is a transition from velocity strengthening at low temperatures, to velocity weakening at intermediate temperatures, and back to velocity strengthening at high temperatures. This behaviour and the restrengthening observed when shearing is stopped are strongly influenced by water content. It is inferred that mechanistic models for the frictional behaviour of gouge-filled faults, under crustal conditions, must account for diffusion and stress corrosion cracking, and for slip on grain boundaries. First attempts to do this, assuming diffusive mass transfer as the fluid-assisted mechanism, successfully predict the steady state and transient behaviour seen in experiments and offer new perspectives for providing friction laws as for modelling earthquake rupture nucleation and evaluating seismic hazard, in the context of both natural and induced seismicity.
Dissolved Organic Carbon 14C in Southern Nevada Groundwater and Implications for Groundwater Travel Times

DOE Office of Scientific and Technical Information (OSTI.GOV)

Hershey, Ronald L.; Fereday, Wyall; Thomas, James M

Dissolved inorganic carbon (DIC) carbon-14 ( 14C) ages must be corrected for complex chemical and physical reactions and processes that change the amount of 14C in groundwater as it flows from recharge to downgradient areas. Because of these reactions, DIC 14C can produce unrealistically old ages and long groundwater travel times that may, or may not, agree with travel times estimated by other methods. Dissolved organic carbon (DOC) 14C ages are often younger than DIC 14C ages because there are few chemical reactions or physical processes that change the amount of DOC 14C in groundwater. However, there are several issuesmore » that create uncertainty in DOC 14C groundwater ages including limited knowledge of the initial (A 0) DOC 14C in groundwater recharge and potential changes in DOC composition as water moves through an aquifer. This study examines these issues by quantifying A 0 DOC 14C in recharge areas of southern Nevada groundwater flow systems and by evaluating changes in DOC composition as water flows from recharge areas to downgradient areas. The effect of these processes on DOC 14C groundwater ages is evaluated and DOC and DIC 14C ages are then compared along several southern Nevada groundwater flow paths. Twenty-seven groundwater samples were collected from springs and wells in southern Nevada in upgradient, midgradient, and downgradient locations. DOC 14C for upgradient samples ranged from 96 to 120 percent modern carbon (pmc) with an average of 106 pmc, verifying modern DOC 14C ages in recharge areas, which decreases uncertainty in DOC 14C A 0 values, groundwater ages, and travel times. The HPLC spectra of groundwater along a flow path in the Spring Mountains show the same general pattern indicating that the DOC compound composition does not change along this flow path. Although DOC concentration decreases from recharge-area to downgradient groundwater, the organic compounds are similar, indicating that DOC 14C is unaffected by other processes such as microbial degradation. A small amount of organic carbon was leached from crushed volcanic and carbonate aquifer outcrop rock in rock-leaching experiments. The leached DOC was high in 14C (75 pmc carbonate rocks, 91 pmc volcanic) suggesting that the leached DOC likely came from microbes in the rock samples. The small amount of DOC and high 14C indicates that the amount of old organic carbon in these rocks is low so there should be minimal impact on groundwater DOC 14C ages. Based on the results from this study, DOC 14C ages do not require additional corrections. Several correction models were applied to DIC 14C ages to correct for water-rock reactions along two carbonate and two volcanic flow paths and the corresponding travel times were compare to DOC 14C travel times. The DOC 14C travel times were hundreds to thousands of years shorter than uncorrected and corrected DIC 14C travel times except for the upper section of one carbonate flow path. DOC 14C travel times ranged from 400 to 5,400 years as compared to DIC 14C that ranged from modern to 20,900 years. The DIC 14C ages are greatly influenced by carbonate mineral and gas reactions and other processes such as matrix diffusion, isotope exchange, or adsorption, which are not always adequately accounted for in DIC 14C groundwater age correction models.« less
Selected data on characteristics of glacial-deposit and carbonate-rock aquifers, midwestern basins and arches region

USGS Publications Warehouse

Joseph, R.L.; Eberts, S.M.

1994-01-01

In 1988, the Geological Survey (USGS) began study to examine the hydrogeologic framework, ground-water-flow systems, water chemistry, and withdrawal response of aquifers in glacial deposits and carbonate rock in the Midwestern Basins and Arches Region in western Ohio and eastern Indiana. As part of this study, data from pumped-well tests and instantaneous-rechange tests (slug tests) of wells completed in the glacial-deposit and carbonate-rock aquifers were compiled from reports and information on file with State agencies, environmental consulting firms, drilling firms, municipalities, universities, and the USGS. The data, from 73 counties in Ohio and Indiana, were entered into a computerized data base in a spreadsheet format and subsequently into a geographic information system (GIS). Aquifer-characteristics data from this compilation include the results of 105 pumped-well tests and 39 slug tests in wells completed in glacial deposits, 174 pumped-well tests in wells completed in the carbonate-rock aquifer, and 4 slug tests in wells completed in limestones and shales of Ordovician age. Transmissivities from the pumped-well tests in wells completed in glacial till and glacial-deposit aquifers (sands and gravels) range from 1.54 to 69,700 feet squared per day. Storage coefficients or specific yields range from 0.00002 to 0.38 at these wells. Horizontal-hydraulic conductivities from the slug tests in wells completed in glacial-deposit aquifers range from 0.33 to 1,000 feet per day. Transmissivities from the pumped-well tests in wells completed in the carbonate-rock aquifer range from 70 to 52,000 feet squared per day. Storage coefficient or specific yields at these wells range from 0.00001 to 0.05. Horizontal hydraulic conductivities from the slug tests in wells completed in limestones and shales of Ordovician age range from 0.0016 to 12 feet per day. These data are summarized in tables and figures within this report. The collection and compilation of selected aquifer-characteristic data for the glacial-deposit and carbonate-rock aquifers within the Midwestern Basin and Arches Region of Shaver (1985) are an essential part of the Midwestern Basins and Arches Regional Aquifer-Systems Analysis (Midwestern Basins and Arches RASA) project of the U.S. Geological Survey (USGS). Specifically, the data are needed to help describe ground-water flow in the regional aquifer system, which isone of the objectives of the Midwestern Basins and Arches RASA project (Bugliosi, 1990). To meet this objective, the Midwestern Basins and Arches RASA began subprojects in the Ohio and Indiana offices of the USGS to collect and compile available aquifer-characteristics data from aquifer tests of the glacial-deposit and carbonate-rock aquifers. The data were not reanalyzed to verify accuracy because of time constraints and insufficient data in many cases.
Experimental investigation of CO2-brine-rock interactions at simulated in-situ conditions

NASA Astrophysics Data System (ADS)

Słomski, Piotr; Lutyński, Marcin; Mastalerz, Maria; Szczepański, Jacek; Derkowski, Arkadiusz; Topór, Tomasz

2017-04-01

Geological sequestration of carbon dioxide (CO2) in deep formations (e.g. saline aquifers, oil and gas reservoirs and coalbeds) is one of the most promising options for reducing concentration of this anthropogenic greenhouse gas in the atmosphere. CO2 injected into the rock formations can be trapped by several mechanisms including structural and stratigraphic trapping, capillary CO2 trapping, dissolution trapping and mineral trapping. During dissolution trapping, CO2 dissolves in the formation brine and sinks in the reservoir as the CO2-enriched brine has an increased density. In comparison, in mineral trapping, CO2 is bound by precipitating new carbonate minerals. The latter two mechanisms depend on the temperature, pressure, and the mineralogy of the reservoir rock and the chemical composition of the brine. This study discusses laboratory scale alterations of Ordovician and Silurian shale rocks from potential CO2 sequestration site B1 in the Baltic Basin. In the reported experiment, rocks submerged in brine in specially constructed reactors were subjected to CO2 pressure of 30-35 MPa for 30-45 days at temperature of 80 oC. Shale samples were analyzed in terms of mineral composition and mesopore surface area and volume, before and after experiments, by means of X-ray diffraction and N2 low-pressure adsorption, respectively, for possible CO2 induced changes. Comparison of mineral composition before and after experiments demonstrated subtle mineral changes. The most conspicuous was a release of Fe in the form of Fe-oxyhydroxides, most probably related to the decomposition of Fe-bearing minerals like pyrite, chlorite and, less frequently, ankerite. With regard to porosity, interestingly, the most significant increase in mesopore surface area and mesopore volume was observed in samples with the largest drop of chlorite amount. The less significant mineral changes were associated with formation of kaolinite related to breakdown of feldspars and dissolution of carbonate minerals represented by calcite, dolomite, and ankerite. In the analyzed samples, no new carbonate minerals were formed during the experiments. An increase of carbonates was recorded only in three out of 13 samples. However, concentration of carbonates in these three samples is too low to conclude CO2 mineral trapping in new carbonate phases. Acknowledgments: the study was supported from grant SHALESEQ (No PL12-0109) funded by the National Centre for Research and Development.
Cross sections showing stratigraphic and depositional lithofacies of upper Cambrian rocks and the relation of lithofacies to potential for Mississippi Valley-type mineralization in the Harrison 1° x 2° quadrangle, Missouri and Arkansas (folio of the Harrison 1 degree by 2 degrees quadrangle, Missouri and Arkansas)

USGS Publications Warehouse

Hayes, Timothy S.; Palmer, James R.; Pratt, Walden P.; Krizanich, Gary; Whitfield, John W.; Seeger, Cheryl M.

1997-01-01

These cross sections are the fifth publication in a folio of maps of the Harrison 1° x 2° quadrangle, Missouri and Arkansas, prepared under the Conterminous United States Mineral Assessment Program (CUSMAP). Previously published maps in this folio relate to the geochemistry of the subsurface carbonate rocks (Erickson and others, 1989), the geophysics of the basement terranes (McCafferty and others, 1989), the sedimentary rocks and mineralization of the Caulfield district (Hayes and others, 1992), the mineral resource potential of the quadrangle (Pratt and others, 1993), and the bedrock geology of the quadrangle (Middendorf and others, 1994 and in press). A final set of maps showing locations of known Mississippi Valley-type deposits and occurrences relative to Late Cambrian shaly lithofacies and other shales in the Harrison and adjoining quadrangle is in preparation (Palmer and Hayes, in press).
Biomass of the cryptoendolithic microbiota from the Antarctic desert

NASA Technical Reports Server (NTRS)

Vestal, J. R.; Friedmann, E. I. (Principal Investigator)

1988-01-01

Extractable lipid phosphate was used to determine the biomass of the cryptoendolithic microbiota that colonizes sandstone rocks in the Ross Desert region of Antarctica. The mean amount of lipid phosphate was 0.053 micromole/cm2 (n = 9), which equals 2.54 g of C per m2 (range, 1.92 to 3.26 g of C per m2) of biomass in the biotic zone of these rocks. The turnover of phospholipids was comparable to that of temperate sediments and soils (t1/2, 6 to 9 days) at 0 degrees C and a light intensity of 305 micromoles of photons per m2 per s, indicating that this was a good method to measure viable biomass. The biomass was 0.3 to 9.6% of the total carbon content of the biotic zone and was about 2 orders of magnitude smaller than the epilithic lichen dry weight at a location some 7 degrees north in latitude. The cryptoendolithic microbiota had a uniform density throughout the biotic zone under the rock surface. The results indicate that the cryptoendolithic microbial biomass is small but viable in this unique, extreme ecosystem.
Experimental evidence for chemo-mechanical coupling during carbon mineralization in ultramafic rocks

NASA Astrophysics Data System (ADS)

Lisabeth, H. P.; Zhu, W.; Kelemen, P. B.; Ilgen, A.

2017-09-01

Storing carbon dioxide in the subsurface as carbonate minerals has the benefit of long-term stability and immobility. Ultramafic rock formations have been suggested as a potential reservoir for this type of storage due to the availability of cations to react with dissolved carbon dioxide and the fast reaction rates associated with minerals common in ultramafic formations; however, the rapid reactions have the potential to couple with the mechanical and hydraulic behavior of the rocks and little is known about the extent and mechanisms of this coupling. In this study, we argue that the dissolution of primary minerals and the precipitation of secondary minerals along pre-existing fractures in samples lead to reductions in both the apparent Young's modulus and shear strength of aggregates, accompanied by reduction in permeability. Hydrostatic and triaxial deformation experiments were run on dunite samples saturated with de-ionized water and carbon dioxide-rich solutions while stress, strain, permeability and pore fluid chemistry were monitored. Sample microstructures were examined after reaction and deformation using scanning electron microscopy (SEM). The results show that channelized dissolution and carbonate mineral precipitation in the samples saturated with carbon dioxide-rich solutions modify the structure of grain boundaries, leading to the observed reductions in stiffness, strength and permeability. A geochemical model was run to help interpret fluid chemical data, and we find that the apparent reaction rates in our experiments are faster than rates calculated from powder reactors, suggesting mechanically enhanced reaction rates. In conclusion, we find that chemo-mechanical coupling during carbon mineralization in dunites leads to substantial modification of mechanical and hydraulic behavior that needs to be accounted for in future modeling efforts of in situ carbon mineralization projects.
Experimental Assessment of Carbon Isotopes of Light Hydrocarbons under Different Redox Conditions

NASA Astrophysics Data System (ADS)

Fu, Q.; Chen, X.

2017-12-01

Hydrocarbons can be derived from a variety of carbon sources, by different processes, and under a wide range of physicochemical conditions. Other than bacterial activities facilitating biogenic hydrocarbon formation at low temperatures, decomposition of complex organic matter in sedimentary rocks at elevated temperatures produce thermogenic hydrocarbons, whereas abiogenic hydrocarbons are mainly generated through Fischer-Tropsch type synthesis with mineral catalysts. The carbon isotope has been used extensively to distinguish hydrocarbons of different origins and their formation conditions. For each type of hydrocarbons, however, environmental conditions may change reaction pathways and corresponding isotope fractionations. To better understand the variation of carbon isotopes caused by environmental variables, mineral constraints in particular, a series of laboratory experiments are conducted. In experiments where thermogenic hydrocarbons are formed, oil shale is the source material with different gypsum contents (0, 0.3, 0.5, and 1 wt.%). The abundance of generated light straight chain hydrocarbons decreases with increasing gypsum content, but their carbon isotopes become heavier. For example, the δ13C value of methane increases from -55.1‰ to -41.4‰ with gypsum varying between 0 and 1 wt.%. In similar experiments with the presence of MnO2, carbon isotope values of light alkanes are also higher, but with limited magnitudes (e.g., 3 to 4‰ for methane). In another experiment with dissolved H2 gas of 100 mmol/kg, light alkanes become depleted in 13C than experiments without H2. For example, there is a depletion of 2.7‰ for methane. The variation of carbon isotope values of light alkanes suggests the redox condition, constrained by mineral assemblage, fluid composition, and physical environment, play an important role in isotope fractionation. The pathway of hydrocarbon generation may be different under oxidized or reducing conditions. A set of experiments, in which abiogenic hydrocarbons are formed, is currently in progress. Combined together, they would facilitate our understanding of carbon isotope fractionation under geological conditions, and effective use of carbon isotopes as a diagnostic tool for hydrocarbons that are poorly understood in terms of origin and evolution.
ATP-stabilized amorphous calcium carbonate nanospheres and their application in protein adsorption.

PubMed

Qi, Chao; Zhu, Ying-Jie; Lu, Bing-Qiang; Zhao, Xin-Yu; Zhao, Jing; Chen, Feng; Wu, Jin

2014-05-28

Calcium carbonate is a common substance found in rocks worldwide, and is the main biomineral formed in shells of marine organisms and snails, pearls and eggshells. Amorphous calcium carbonate (ACC) is the least stable polymorph of calcium carbonate, which is so unstable under normal conditions that it is difficult to be prepared in vitro because it rapidly crystallizes to form one of the more stable polymorphs in aqueous solution. Herein, we report the successful synthesis of highly stable ACC nanospheres in vitro using adenosine 5'-triphosphate disodium salt (ATP) as a stabilizer. The effect of ATP on the stability of ACC nanospheres is investigated. Our experiments show that ATP plays an unique role in the stabilization of ACC nanospheres in aqueous solution. Moreover, the as-prepared ACC nanospheres are highly stable in phosphate buffered saline for a relatively long period of time (12 days) even under relatively high concentrations of calcium and phosphate ions. The cytotoxicity tests show that the as-prepared highly stable ACC nanospheres have excellent biocompatibility. The highly stable ACC nanospheres have high protein adsorption capacity, implying that they are promising for applications in biomedical fields such as drug delivery and protein adsorption. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Sinkhole development resulting from ground-water withdrawal in the Tampa area, Florida

USGS Publications Warehouse

Sinclair, William C.

1982-01-01

The area of municipal well fields on the Gulf Coastal Plain north of tampa, Fla., is densely pitted with natural sinkholes and sinkhole lakes that have resulted from collapse of surficial sand and clay into solution cavities in the underlying carbonate rocks of the Floridan aquifer. Although solution of the underlying rocks is the ultimate cause of sinkholes, some have been induced by abrupt changes in ground-water levels caused by pumping. Declines in water levels cause loss of support to the bedrock roofs over cavities and to surficial material overlying openings in the top of bedrock. The volume of calcium, magnesium , and carbonate (the constituents of limestone and dolomite) in solution in the water withdrawn from four well fields near Tampa totaled about 240,000 cubic feet in 1978. Most induced solution takes place at the limestone surface however, and the area of induced recharge is so extensive that the effect of induced limestone solution on sinkhole development is negligible. Alinement of established sinkholes along joint patterns in the bedrock suggests that a well along these lineations might have direct hydraulic connection with a zone of incipient sinkholes. Therefore, pumping of large-capacity wells along such lineations would increase the probability of sinkhole development. Although sinkholes generally form abruptly in the study area, local changes such as vegetative stress, ponding of rainfall, misalinement of structures, and turbidity in well water are all indications that percollapse subsidence may be taking place. (USGS)
Reduction of nitrogen compounds in oceanic basement and its implications for HCN formation and abiotic organic synthesis

PubMed Central

2009-01-01

Hydrogen cyanide is an excellent organic reagent and is central to most of the reaction pathways leading to abiotic formation of simple organic compounds containing nitrogen, such as amino acids, purines and pyrimidines. Reduced carbon and nitrogen precursor compounds for the synthesis of HCN may be formed under off-axis hydrothermal conditions in oceanic lithosphere in the presence of native Fe and Ni and are adsorbed on authigenic layer silicates and zeolites. The native metals as well as the molecular hydrogen reducing CO2 to CO/CH4 and NO3-/NO2- to NH3/NH4+ are a result of serpentinization of mafic rocks. Oceanic plates are conveyor belts of reduced carbon and nitrogen compounds from the off-axis hydrothermal environments to the subduction zones, where compaction, dehydration, desiccation and diagenetic reactions affect the organic precursors. CO/CH4 and NH3/NH4+ in fluids distilled out of layer silicates and zeolites in the subducting plate at an early stage of subduction will react upon heating and form HCN, which is then available for further organic reactions to, for instance, carbohydrates, nucleosides or even nucleotides, under alkaline conditions in hydrated mantle rocks of the overriding plate. Convergent margins in the initial phase of subduction must, therefore, be considered the most potent sites for prebiotic reactions on Earth. This means that origin of life processes are, perhaps, only possible on planets where some kind of plate tectonics occur. PMID:19849830
Reduction of nitrogen compounds in oceanic basement and its implications for HCN formation and abiotic organic synthesis.

PubMed

Holm, Nils G; Neubeck, Anna

2009-10-22

Hydrogen cyanide is an excellent organic reagent and is central to most of the reaction pathways leading to abiotic formation of simple organic compounds containing nitrogen, such as amino acids, purines and pyrimidines. Reduced carbon and nitrogen precursor compounds for the synthesis of HCN may be formed under off-axis hydrothermal conditions in oceanic lithosphere in the presence of native Fe and Ni and are adsorbed on authigenic layer silicates and zeolites. The native metals as well as the molecular hydrogen reducing CO2 to CO/CH4 and NO3-/NO2- to NH3/NH4+ are a result of serpentinization of mafic rocks. Oceanic plates are conveyor belts of reduced carbon and nitrogen compounds from the off-axis hydrothermal environments to the subduction zones, where compaction, dehydration, desiccation and diagenetic reactions affect the organic precursors. CO/CH4 and NH3/NH4+ in fluids distilled out of layer silicates and zeolites in the subducting plate at an early stage of subduction will react upon heating and form HCN, which is then available for further organic reactions to, for instance, carbohydrates, nucleosides or even nucleotides, under alkaline conditions in hydrated mantle rocks of the overriding plate. Convergent margins in the initial phase of subduction must, therefore, be considered the most potent sites for prebiotic reactions on Earth. This means that origin of life processes are, perhaps, only possible on planets where some kind of plate tectonics occur.
Empirical relations of rock properties of outcrop and core samples from the Northwest German Basin for geothermal drilling

NASA Astrophysics Data System (ADS)

Reyer, D.; Philipp, S. L.

2014-09-01

Information about geomechanical and physical rock properties, particularly uniaxial compressive strength (UCS), are needed for geomechanical model development and updating with logging-while-drilling methods to minimise costs and risks of the drilling process. The following parameters with importance at different stages of geothermal exploitation and drilling are presented for typical sedimentary and volcanic rocks of the Northwest German Basin (NWGB): physical (P wave velocities, porosity, and bulk and grain density) and geomechanical parameters (UCS, static Young's modulus, destruction work and indirect tensile strength both perpendicular and parallel to bedding) for 35 rock samples from quarries and 14 core samples of sandstones and carbonate rocks. With regression analyses (linear- and non-linear) empirical relations are developed to predict UCS values from all other parameters. Analyses focus on sedimentary rocks and were repeated separately for clastic rock samples or carbonate rock samples as well as for outcrop samples or core samples. Empirical relations have high statistical significance for Young's modulus, tensile strength and destruction work; for physical properties, there is a wider scatter of data and prediction of UCS is less precise. For most relations, properties of core samples plot within the scatter of outcrop samples and lie within the 90% prediction bands of developed regression functions. The results indicate the applicability of empirical relations that are based on outcrop data on questions related to drilling operations when the database contains a sufficient number of samples with varying rock properties. The presented equations may help to predict UCS values for sedimentary rocks at depth, and thus develop suitable geomechanical models for the adaptation of the drilling strategy on rock mechanical conditions in the NWGB.
Editorial

NASA Astrophysics Data System (ADS)

Agosta, Fabrizio; Luetkemeyer, P. Benjamin; Lamarche, Juliette; Crider, Juliet G.; Lacombe, Olivier

2016-10-01

The present Volume is after the 2015 EGU General Assembly, held in Vienna (Austria), where we convened a session entitled "The role of fluids in faulting and fracturing in carbonates and other upper crustal rocks". In that occasion, more than forty contributions were illustrated as oral and poster presentations. The invitation to contribute to this Volume was extended not only to the session participants, but also to a wider spectrum of researchers working on related topics. As a result, a group of Earth scientists encompassing geologists, geophysicists, geochemists and petrologists contributed to this Volume, providing a sampling of the state-of-the-science on fluids and faulting in carbonate, crystalline and siliciclastic rocks from studies that combine and integrate different methods, including rock mechanics, petrophysics, structural diagenesis and crustal permeability.
Replication in plastic of three-dimensional fossils preserved in indurated clastic sedimentary rocks

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zapasink, H.T.; Johnston, P.A.

A new technique for replicating in plastic the fossils preserved in clastic rocks should now make available reliable morphologic and frequency data, comparable in quality to those derived from acid-prepared silicified faunas, for a major segment of the fossil record. The technique involves 3 steps: the dissolution of carbonate in fossiliferous rocks with hydrochloric acid, impregnation of resulting voids with liquid plastic, and dissolution of the rock matrix with hydrofluoric acid, leaving a concentrate of plastic-replaced fossils.
Mineral and energy resources of the Roswell Resource Area, East-Central New Mexico

USGS Publications Warehouse

Bartsch-Winkler, Susan B.; Donatich, Alessandro J.

1995-01-01

The sedimentary formations of the Roswell Resource Area have significant mineral and energy resources. Some of the pre-Pennsylvanian sequences in the Northwestern Shelf of the Permian Basin are oil and gas reservoirs, and Pennsylvanian rocks in Tucumcari Basin are reservoirs of oil and gas as well as source rocks for oil and gas in Triassic rocks. Pre-Permian rocks also contain minor deposits of uranium and vanadium, limestone, and gases. Hydrocarbon reservoirs in Permian rocks include associated gases such as carbon dioxide, helium, and nitrogen. Permian rocks are mineralized adjacent to the Lincoln County porphyry belt, and include deposits of copper, uranium, manganese, iron, polymetallic veins, and Mississippi-Valley-type lead-zinc. Industrial minerals in Permian rocks include fluorite, barite, potash, halite, polyhalite, gypsum, anhydrite, sulfur, limestone, dolomite, brine deposits (iodine and bromine), aggregate (sand), and dimension stone. Doubly terminated quartz crystals, called 'Pecos diamonds' and collected as mineral specimens, occur in Permian rocks along the Pecos River. Mesozoic sedimentary rocks are hosts for copper, uranium, and small quantities of gold-silver-tellurium veins, as well as significant deposits of oil and gas, carbon dioxide, asphalt, coal, and dimension stone. Mesozoic rocks contain limited amounts of limestone, gypsum, petrified wood, and clay. Tertiary rocks host ore deposits commonly associated with intrusive rocks, including platinum-group elements, iron skarns, manganese, uranium and vanadium, molybdenum, polymetallic vein deposits, gold-silver-tellurium veins, and thorium-rare-earth veins. Museum-quality quartz crystals are associated with Tertiary intrusive rocks. Industrial minerals in Tertiary rocks include fluorite, vein- and bedded-barite, caliche, limestone, and aggregate. Tertiary and Quaternary sediments host important placer deposits of gold and titanium, and occurrences of silver and uranium. Important industrial commodities include caliche, limestone and dolomite, and aggregate. Quaternary basalt contains sub-ore-grade uranium, scoria, and clay deposits.
Application of fluorinated nanofluid for production enhancement of a carbonate gas-condensate reservoir through wettability alteration

NASA Astrophysics Data System (ADS)

Sakhaei, Zahra; Azin, Reza; Naghizadeh, Arefeh; Osfouri, Shahriar; Saboori, Rahmatollah; Vahdani, Hosein

2018-03-01

Condensate blockage phenomenon in near-wellbore region decreases gas production rate remarkably. Wettability alteration using fluorinated chemicals is an efficacious way to vanquish this problem. In this study, new synthesized fluorinated silica nanoparticles with an optimized condition and mean diameter of 50 nm is employed to modify carbonate rock surface wettability. Rock characterization tests consisting Field Emission Scanning Electron Microscopy (FE-SEM) and Energy Dispersive x-ray Spectroscopy (EDX) were utilized to assess the nanofluid adsorption on rock surface after treatment. Contact angle, spontaneous imbibition and core flooding experiments were performed to investigate the effect of synthesized nanofluid adsorption on wettability of rock surface and liquid mobility. Results of contact angle experiments revealed that wettability of rock could alter from strongly oil-wetting to the intermediate gas-wetting even at elevated temperature. Imbibition rates of oil and brine were diminished noticeably after treatment. 60% and 30% enhancement in pressure drop of condensate and brine floods after wettability alteration with modified nanofluid were observed which confirm successful field applicability of this chemical.
Greenhouse Gases and Energy Intensity of Granite Rock Mining Operations in Thailand: A Case of Industrial Rock-Construction

NASA Astrophysics Data System (ADS)

Kittipongvises, Suthirat; Chavalparit, Orathai; Sutthirat, Chakkaphan

2016-12-01

This paper is aimed to systematically assess greenhouse gases (GHGs) and energy intensity of the granite rock mining operations in Thailand and also identify a range of feasible options to minimize their GHG emissions. Mining factories A, B and C, located in the Eastern region of Thailand, were selected as research case studies. The results indicated that the 3-year average of GHGs emissions from factories A to C was 3387 718 kgCO2e per year with approximately 2.92 kgCO2e per ton of granite rock produced over 2012 to 2014. Of this, the carbon intensity of grid-electricity consumption for the crushed rock production was 1.84 kgCO2/kWh. Diesel fuel combustion for transport activities in the mining factories was the greatest contributor to GHGs emissions (68 %) compared to the purchased electricity and explosion process, with 31 % and 1 %, respectively. In-Pit Crushing and Conveying (IPCC) installation, haul truck payload optimization and management, and reduction in tire rolling resistance have shown potential to reduce carbon emissions accounted for 20 % to 70 %.

Serpentinization and fluid-rock interaction in Jurassic mafic and ultramafic sea-floor: constraints from Ligurian ophiolite sequences

NASA Astrophysics Data System (ADS)

Vogel, Monica; Früh-Green, Gretchen L.; Boschi, Chiara; Schwarzenbach, Esther M.

2014-05-01

The Bracco-Levanto ophiolitic complex (Eastern Liguria) represents one of the largest and better-exposed ophiolitic successions in the Northern Apennines. It is considered to be a fragment of heterogeneous Jurassic lithosphere that records tectono-magmatic and alteration histories similar to those documented along the Mid-Atlantic Ridge, such as at the 15°20'N area and the Atlantis Massif at 30°N. Structural and petrological studies on these rocks provide constraints on metamorphic/deformation processes during formation and hydrothermal alteration of the Jurassic oceanic lithosphere. We present a petrological and geochemical study of deformation processes and fluid-rock interaction in the Bracco-Levanto ophiolitic complex and compare these to modern oceanic hydrothermal systems, such as the Lost City Hydrothermal Field hosted in ultramafic rocks on the Atlantis Massif. A focus is on investigating mass transfer and fluid flow paths during high and low temperature hydrothermal activity, and on processes leading to hydrothermal carbonate precipitation and the formation of ophicalcites, which are characteristic of the Bracco-Levanto sequences. Major element and mineral compositional data allow us to distinguish a multiphase history of alteration characterized by: (1) widespread SiO2 metasomatism during progressive serpentinization, and (2) multiple phases of veining and carbonate precipitation associated with circulation of seawater and high fluid-rock ratios in the shallow ultramafic-dominated portions of the Jurassic seafloor. We observe regional variations in MgO, SiO2 and Al2O3, suggesting Si-flux towards stratigraphically higher units. In general, the ophicalcites have higher Si, Al and Fe concentrations and lower Mg than the serpentinite basement rocks or serpentinites with minimal carbonate veins. Bulk rock trace element data and Sr isotope ratios indicate seawater reacting with rocks of more mafic composition, then channeled towards stratigraphically higher units, leading to Si metasomatism in the serpentinites and ophicalcites. Channelling of Si-rich fluids is also indicated by amphibole and talc growth in shear zones and wall rock around the ophicalcites. δ18O-values of the carbonate veins indicate temperatures up to 150°C and document a decrease in temperature with ongoing serpentinization. Comparison with serpentinites from the Atlantis Massif and 15°20'N indicates a similar degree of Si enrichment in the modern seafloor and suggests that Si-metasomatism may be a fundamental process associated with serpentinization at slow-spreading ridge environments.
Evaluating Uranium Isotopes in Carbonates and Implications for Reconstructing Marine Paleoredox Conditions

NASA Astrophysics Data System (ADS)

Aharony, Ofer; Gubser, Steven S.; Maldacena, Juan; Ooguri, Hirosi; Oz, Yaron

2016-12-01

Uranium isotope ratios (238U/235U, reported as δ238U) have emerged as a promising proxy for marine redox conditions. This proxy relies on isotopic fractionation that occurs during reduction of soluble U(VI) to insoluble U(IV), wherein 238U is preferentially reduced and incorporated via authigenic processes into anoxic sediments, leaving the residual seawater U and resulting carbonates 238U-depleted. Because carbonates are generally well preserved in the rock record, they are useful archives of seawater chemistry throughout Earth history, including δ238U. In principle, the long residence time of U in the ocean permits quantitative inferences of global paleoredox conditions using carbonate δ238U records. To assess the performance of the proxy, we compile all published δ238U measurements from carbonate rocks and sediments, which span the Cryogenian through the modern. The potential for δ238U to serve as a quantitative, global paleoredox proxy is supported by reproducible trends across depositional environments and paleogeographic regions in the Cryogenian non-glacial interlude and across the Permian-Triassic and Triassic-Jurassic boundaries, although carbonates deposited in deeper waters (>200 m) may be subject to local effects. Using a box model, we highlight the key levers associated with seawater δ238U and the timescales of such variability. Like all sedimentary archives, carbonate rocks are prone to diagenetic alteration and additional controls that cause δ238U in carbonates to deviate from global seawater values. Specifically, the U isotopic composition of carbonate sediments can be influenced by diagenesis, carbonate mineralogy, dolomitization, detrital input, local organic matter deposition, and pore water chemistry. We evaluate indicators of these factors in the context of a diagenetic model to assess the sensitivity of carbonate δ238U to local syndepositional or post-depositional processes. These results improve the framework for interpreting carbonate δ238U records and reconstructing past changes in the oxygenation of the Earth's oceans.
Calibration of NMR well logs from carbonate reservoirs with laboratory NMR measurements and μXRCT

DOE PAGES

Mason, Harris E.; Smith, Megan M.; Hao, Yue; ...

2014-12-31

The use of nuclear magnetic resonance (NMR) well log data has the potential to provide in-situ porosity, pore size distributions, and permeability of target carbonate CO₂ storage reservoirs. However, these methods which have been successfully applied to sandstones have yet to be completely validated for carbonate reservoirs. Here, we have taken an approach to validate NMR measurements of carbonate rock cores with independent measurements of permeability and pore surface area to volume (S/V) distributions using differential pressure measurements and micro X-ray computed tomography (μXRCT) imaging methods, respectively. We observe that using standard methods for determining permeability from NMR data incorrectlymore » predicts these values by orders of magnitude. However, we do observe promise that NMR measurements provide reasonable estimates of pore S/V distributions, and with further independent measurements of the carbonate rock properties that universally applicable relationships between NMR measured properties may be developed for in-situ well logging applications of carbonate reservoirs.« less
Calibration of NMR well logs from carbonate reservoirs with laboratory NMR measurements and μXRCT

DOE Office of Scientific and Technical Information (OSTI.GOV)

Mason, Harris E.; Smith, Megan M.; Hao, Yue

The use of nuclear magnetic resonance (NMR) well log data has the potential to provide in-situ porosity, pore size distributions, and permeability of target carbonate CO₂ storage reservoirs. However, these methods which have been successfully applied to sandstones have yet to be completely validated for carbonate reservoirs. Here, we have taken an approach to validate NMR measurements of carbonate rock cores with independent measurements of permeability and pore surface area to volume (S/V) distributions using differential pressure measurements and micro X-ray computed tomography (μXRCT) imaging methods, respectively. We observe that using standard methods for determining permeability from NMR data incorrectlymore » predicts these values by orders of magnitude. However, we do observe promise that NMR measurements provide reasonable estimates of pore S/V distributions, and with further independent measurements of the carbonate rock properties that universally applicable relationships between NMR measured properties may be developed for in-situ well logging applications of carbonate reservoirs.« less
The effect of mineral composition on the sorption of cesium ions on geological formations.

PubMed

Kónya, József; Nagy, Noémi M; Nemes, Zoltán

2005-10-15

The sorption of cesium-137 on rock samples, mainly on clay rocks, is determined as a function of the mineral composition of the rocks. A relation between the mineral groups (tectosilicates, phyllosilicates, clay minerals, carbonates) and their cesium sorption properties is shown. A linear model is constructed by which the distribution coefficients of the different minerals can be calculated from the mineral composition and the net distribution coefficient of the rock. On the basis of the distribution coefficients of the minerals the cesium sorption properties of other rocks can be predicted.
Karst in Wadi Bani Khalid, Oman

NASA Astrophysics Data System (ADS)

Abdelaziz, Ramadan

2017-04-01

There are several important in Oman. The main aquifer is surficial aquifer and fractured rocks. In fact, the geology of Oman is complex whichmake the hydraulic continuity of bedrock is limited and formaing localized aquifers. caves in Oman are varying types and length, size and geographic formations. Many caves and valleys founded in Oman. Wadi Bani Khalid hosts complex network of fractured rock. Karst in Wadi Bani Kalid made upof Limestone(Calcium, which is dissolve in water.A rain water pass through the rock it is erode the rock and form caves. The cave located in Miqil. The karst was formed in Calcium Carbonate rocks.
Dissolution of salt on the east flank of the Permian Basin in the southwestern U.S.A.

USGS Publications Warehouse

Johnson, K.S.

1981-01-01

Hydrogeologic studies prove that natural dissolution of bedded salt occurs at shallow depths in many parts of the Permian Basin of the southwestern U.S.A. This is especially well-documented on the east side of the basin in study areas on the Cimarron River and Elm Fork in western Oklahoma, and on the Red River in the southeastern part of the Texas Panhandle. Four requirements for salt dissolution are: (1) a deposit of salt; (2) a supply of water unsaturated with respect to NaCl; (3) an outlet for removal of brine; and (4) energy to cause water to flow through the system. The supply of fresh groundwater in the region is recharged through permeable rocks, alluvium, terrace deposits, karstic features and fractures. Groundwater dissolves salt at depths of 10-250 m, and the resulting brine moves laterally and upward under hydrostatic pressure through caverns, fractures in disrupted rock, and clastic or carbonate aquifers until it reaches the land surface, where it forms salt plains and salt springs. In many areas, salt dissolution produces a self-perpetuating cycle: dissolution causes cavern development, followed by collapse and subsidence of overlying rock; then the resulting disrupted rock has a greater vertical permeability that allows increased water percolation and additional salt dissolution. ?? 1981.
Reactivity of dissolved- vs. supercritical-CO2 phase toward muscovite basal surfaces

NASA Astrophysics Data System (ADS)

Wan, J.; Tokunaga, T. K.; Kim, Y.; Wang, S.; Altoe, M. V. P.; Ashby, P. D.; DePaolo, D.

2015-12-01

The current understanding of geochemical reactions in reservoirs for geological carbon sequestration (GCS) is largely based on aqueous chemistry (CO2 dissolves in reservoir brine and brine reacts with rocks). However, only a portion of the injected supercritical (sc) CO2 dissolves before the buoyant plume contacts caprock, where it is expected to reside for a long time. Although numerous studies have addressed scCO2-mineral reactions occurring within adsorbed aqueous films, possible reactions resulting from direct CO2-rock contact remain less understood. Does CO2 as a supercritical phase react with reservoir rocks? Do mineral react differently with scCO2 than with dissolved CO2? We selected muscovite, one of the more stable and common rock-forming silicate minerals, to react with scCO2 phase (both water-saturated and water-free) and compared with CO2-saturated-brine. The reacted basal surfaces were analyzed using atomic force microscopy and X-ray photoelectron spectroscopy for examining the changes in surface morphology and chemistry. The results show that scCO2 (regardless of its water content) altered muscovite considerably more than CO2-saturated brine; suggest CO2 diffusion into mica interlayers and localized mica dissolution into scCO2 phase. The mechanisms underlying these observations and their implications for GCS need further exploration.
Ordovician of the Sauk megasequence in the Ozark region of northern Arkansas and parts of Missouri and adjacent states: Chapter 11

USGS Publications Warehouse

Ethington, Raymond L.; Repetski, John E.; Derby, James R.

2012-01-01

The oldest formation that crops out in the region is the Jefferson City Dolomite, which may be present in outcrops along incised river valleys near the Missouri-Arkansas border. Rare fossil gastropods, bivalves, brachiopods, conodonts, and trilobites permit correlation of the Cotter through Powell Dolomites with Ibexian strata elsewhere in Laurentia. Conodonts in the Black Rock Limestone Member of the Smithville Formation and the upper part of the Powell Dolomite confirm regional relationships that have been suggested for these units; those of the Black Rock Limestone Member are consistent with deposition under more open marine conditions than existed when older and younger units were forming. Brachiopods and conodonts from the overlying Everton Formation assist in interpreting complex facies within that formation and its correlation to equivalent rocks elsewhere. The youngest conodonts in the Everton Formation provide an age limit for the Sauk-Tippecanoe unconformity near the southern extremity of the great American carbonate bank. The correlation to coeval strata in the Ouachita Mountains of central Arkansas and in the Arbuckle Mountains of Oklahoma and to rocks penetrated in wells drilled in the Reelfoot rift basin has been improved greatly in recent years by integration of biostratigraphic data with lithologic information.
Deformation associated to exhumation of serpentinized mantle rocks in a fossil Ocean Continent Transition: The Totalp unit in SE Switzerland

NASA Astrophysics Data System (ADS)

Picazo, S.; Manatschal, G.; Cannat, M.; Andréani, M.

2013-08-01

Although the exhumation of ultramafic rocks in slow and ultraslow spreading Mid-Ocean Ridges and Ocean Continent Transitions (OCTs) has been extensively investigated, the deformation processes related to mantle exhumation are poorly constrained. In this paper we present a new geological map and a section across the exhumed serpentinized peridotites of the Totalp unit near Davos (SE Switzerland), and we propose that the Totalp unit is formed by two Alpine thrust sheets. Geological mapping indicates local exposure of a paleo-seafloor that is formed by an exhumed detachment surface and serpentinized peridotites. The top of the exhumed mantle rocks is made of ophicalcites that resulted from the carbonation of serpentine under static conditions at the seafloor. The ophicalcites preserve depositional contacts with Upper Jurassic to Lower Cretaceous pelagic sediments (Bernoulli and Weissert, 1985). These sequences did not exceed prehnite-pumpellyite metamorphic facies conditions, and locally escaped Alpine deformation. Thin mylonitic shear zones as well as foliated amphibole-bearing ultramafic rocks have been mapped. The age of these rocks and the link with the final exhumation history are yet unknown but since amphibole-bearing ultramafic rocks can be found as clasts in cataclasites related to the detachment fault, they pre-date detachment faulting. Our petrostructural study of the exhumed serpentinized rocks also reveals a deformation gradient from cataclasis to gouge formation within 150 m in the footwall of the proposed paleo-detachment fault. This deformation postdates serpentinization. It involves a component of plastic deformation of serpentine in the most highly strained intervals that has suffered pronounced grain-size reduction and a polyphase cataclastic overprint.
Uranium mobility during interaction of rhyolitic obsidian, perlite and felsite with alkaline carbonate solution: T = 120° C, P = 210 kg/cm2

USGS Publications Warehouse

Zielinski, Robert A.

1979-01-01

Well-characterized samples of rhyolitic obsidian, perlite and felsite from a single lava flow are leached of U by alkaline oxidizing solutions under open-system conditions. Pressure, temperature, flow rate and solution composition are held constant in order to evaluate the relative importance of differences in surface area and crystallinity. Under the experimental conditions U removal from crushed glassy samples proceeds by a mechanism of glass dissolution in which U and silica are dissolved in approximately equal weight fractions. The rate of U removal from crushed glassy samples increases with decreasing average grain size (surface area). Initial rapid loss of a small component (≈ 2.5%) of the total U from crushed felsite. followed by much slower U loss, reflects variable rates of attack of numerous uranium sites. The fractions of U removed during the experiment ranged from 3.2% (felsite) to 27% (perlite). An empirical method for evaluating the relative rate of U loss from contemporaneous volcanic rocks is presented which incorporates leaching results and rock permeability data.
Petroleum geology and resources of the Nepa-Botuoba High, Angara-Lena Terrace, and Cis-Patom Foredeep, southeastern Siberian Craton, Russia

USGS Publications Warehouse

Ulmishek, Gregory F.

2001-01-01

Three structural provinces of this report, the Nepa-Botuoba High, the Angara-Lena Terrace, and the Cis-Patom Foredeep, occupy the southeastern part of the Siberian craton northwest of the Baikal-Patom folded region (fig. 1). The provinces are similar in many aspects of their history of development, stratigraphic composition, and petroleum geology characteristics. The sedimentary cover of the provinces overlies the Archean?Lower Proterozoic basement of the Siberian craton. Over most of the area of the provinces, the basement is covered by Vendian (uppermost Proterozoic, 650?570 Ma) clastic and carbonate rocks. Unlike the case in the more northwestern areas of the craton, older Riphean sedimentary rocks here are largely absent and they appear in the stratigraphic sequence only in parts of the Cis-Patom Foredeep province. Most of the overlying sedimentary section consists of Cambrian and Ordovician carbonate and clastic rocks, and it includes a thick Lower Cambrian salt-bearing formation. Younger rocks are thin and are present only in marginal areas. 1 A single total petroleum system (TPS) embraces all three provinces. The TPS is unique in two aspects: (1) its rich hydro-carbon reserves are derived from Precambrian source rocks and (2) preservation of oil and gas fields is extremely long owing to the presence of the Lower Cambrian undeformed salt seal. Discovered reserves of the TPS are about 2 billion barrels of oil and more than 30 trillion cubic feet of gas. The stratigraphic distribution of oil and gas reserves is narrow; all fields are in Vendian to lowermost Cambrian clastic and carbonate reservoirs that occur below Lower Cambrian salt. Both structural and stratigraphic traps are known. Source rocks are absent in the sedimentary cover of the provinces, with the possible exception of a narrow zone on the margin of the Cis-Patom Foredeep province. Source rocks are interpreted here to be Riphean and Vendian organic-rich shales of the Baikal-Patom folded region. These rocks presently are deformed and metamorphosed, but they generated oil and gas before the deformation occurred in Late Silurian and Devonian time. Generated hydrocarbons migrated updip onto the craton margin. The time of migration and formation of fields is constrained by the deposition of Lower Cambrian salt and by the Late Silurian or Devonian metamorphism of source rocks. This time frame indicates that the TPS is one of the oldest petroleum systems in the world. All three provinces are exploration frontiers, and available geologic data are limited; therefore, only one assessment unit has been identified. The largest undiscovered hydrocarbon resources are expected to be in Vendian clastic reservoirs in both structural and stratigraphic traps of the Nepa-Botuoba High province. The petroleum potential of Vendian?lowermost Cambrian carbonate reservoirs is smaller. Nevertheless, these reservoirs may contain significant resources. Gas is expected to dominate over oil in the resource base.
Subduction Metamorphism of Ophicarbonates beyond the Stability of Antigorite: insights into Carbonate Dissolution vs. Decarbonation from the Almirez ultramafic massif (S. Spain)

NASA Astrophysics Data System (ADS)

Menzel, Manuel; Garrido, Carlos J.; López Sánchez Vizcaíno, Vicente; Marchesi, Claudio; Hidas, Károly

2017-04-01

Subduction zone processes play a key role in determining the time and length-scales of long-term element cycles like the deep carbon cycle. Recent improvements in thermodynamic modelling of fluid properties at high pressure and new experiments have underlined the importance of carbonate dissolution by subduction fluids from dehydration reactions for the transfer of carbon out of the subducting slab. However, natural case studies are scarce, in particular regarding the impact of fluids generated by serpentinite dehydration, which are considered as a major dissolution agent for carbon due to the high temperature of antigorite breakdown (about 650°C) and the potentially large volumes of hydrated peridotites occurring in the upper part of the subducting oceanic mantle lithosphere. Here we report the occurrence of meta-ophicarbonate lenses within prograde Chl-harzburgites in the Almirez ultramafic massif (Betic Cordillera, S. Spain). The presence of these lenses indicates that carbonate minerals were preserved beyond the stability conditions of antigorite and were not dissolved by deserpentinization fluids. The largest meta-ophicarbonate lens in the Almirez Chl-harzburgites measures 8 x 160 m and is composed of a high-grade assemblage of olivine, Ti-clinohumite, diopside, chlorite, dolomite, calcite and Cr-bearing magnetite with a granofelsic to banded appearance. In this assemblage we identified, for the first time in the Betic Cordillera, aragonite inclusions in olivine and diopside using coupled EBSD and chemical mapping. Calcite-dolomite thermometry and thermodynamic equilibrium modelling constrain the peak metamorphic conditions to 1.7 - 1.9 GPa and 680 °C at very low XCO2. These conditions compare well with P-T-estimates for the surrounding Chl-harzburgites. There is strong evidence that the protolith of the carbonate rocks within Chl-harzburgites was an ophicarbonate zone: bulk rock contents of Ni and Cr are similarly high in the carbonate rocks as in Atg-serpentinites and Chl-harzburgites of the Almirez massif, and their major element compositions plot on the CaCO3-antigorite mixing line. As the meta-ophicarbonates are enclosed within prograde Chl-harzburgites, they have experienced a high fluid flux triggered by the antigorite breakdown in surrounding serpentinites at about 660 °C, with a high potential to dissolve carbonates. However, these carbonate lenses retain high amounts of dolomite and calcite (40 - 45 vol%), and their phase assemblages and stable isotope compositions of carbonate (δ18O = 13-17 ‰ V-SMOW and δ13C = -0.5-1 ‰ V-PDB) do not indicate a major fluid-induced decarbonation. The survival of carbonate may be due to the fact that antigorite dehydration occurred at up to 50 - 70 °C lower temperatures in the presence of CaCO3 than in pure serpentinites. This could lead to the formation of a relatively impermeable shell of carbonate-bearing olivine-diopside fels around the meta-ophicarbonates prior to the main serpentinite dehydration, thus protecting the carbonate-richer assemblages from dissolution. The example of the meta-ophicarbonates at Almirez suggests that this mechanism may lead to recycling of substantial amounts of carbon into the deep mantle via subduction of carbonate-bearing serpentinites. Funding: We acknowledge funding from the People programme (Marie Curie Actions - ITN) of the European Union FP7 under REA Grant Agreement n°608001.
The Impact of Mineralogy on the Geochemical Alteration of Shales During Hydraulic Fracturing Operations

NASA Astrophysics Data System (ADS)

Maher, K.; Harrison, A. L.; Jew, A. D.; Dustin, M. K.; Kiss, A. M.; Kohli, A. H.; Thomas, D.; Joe-Wong, C. M.; Brown, G. E.; Bargar, J.

2016-12-01

The extraction of oil and gas resources from low permeability shale reservoirs using hydraulic fracturing techniques has increased significantly in recent years. During hydraulic fracturing, large volumes of fluid are injected into subsurface shale formations, which drives substantial fluid-rock interaction that can release contaminants and alter rock permeability. Here, a combined experimental, imaging, and modeling approach was employed to systematically evaluate the impact of shale mineralogy on its physical and chemical alteration when exposed to fracturing fluids of different composition. Batch reactor experiments contained different shales with unique mineralogical compositions that were exposed to simulated hydraulic fracturing fluid. Experiments revealed that the balance between fluid acidity and acid neutralizing capacity of the rock was the strongest control on the evolution of fluid and rock chemistry. Carbonate mineral-rich shales rapidly recovered solution pH to circum-neutral conditions, whereas fluids in contact with carbonate mineral-poor shales remained acidic. The dissolution of shale minerals released metal contaminants, yet the precipitation of Fe(III)-bearing secondary phases helped to attenuate their release via co-precipitation or sorption. Post-reaction imaging illustrated that selective dissolution of carbonate minerals generated secondary porosity, the connectivity of which was dictated by initial carbonate distribution. Conversely, the precipitation of secondary Al- and Fe-bearing phases may occlude porosity, potentially inhibiting transport of water, contaminants, and hydrocarbons. The maturation of secondary Fe-bearing phases from amorphous to crystalline over time suggests that porosity will continue to evolve even after oxidation reactions have effectively ceased. These experiments reveal that the relative abundance and distribution of carbonate minerals is the master variable dictating both porosity alteration and contaminant release from shale formations, implying that the response of a reservoir to hydraulic fracturing can be better assessed using robust mineralogical data.
Hydrogeologic framework of fractured sedimentary rock, Newark Basin, New Jersey

USGS Publications Warehouse

Lacombe, Pierre J.; Burton, William C.

2010-01-01

The hydrogeologic framework of fractured sedimentary bedrock at the former Naval Air Warfare Center (NAWC), Trenton, New Jersey, a trichloroethylene (TCE)-contaminated site in the Newark Basin, is developed using an understanding of the geologic history of the strata, gamma-ray logs, and rock cores. NAWC is the newest field research site established as part of the U.S. Geological Survey Toxic Substances Hydrology Program, Department of Defense (DoD) Strategic Environmental Research and Development Program, and DoD Environmental Security Technology Certification Program to investigate contaminant remediation in fractured rock. Sedimentary bedrock at the NAWC research site comprises the Skunk Hollow, Byram, and Ewing Creek Members of the Lockatong Formation and Raven Rock Member of the Stockton Formation. Muds of the Lockatong Formation that were deposited in Van Houten cycles during the Triassic have lithified to form the bedrock that is typical of much of the Newark Basin. Four lithotypes formed from the sediments include black, carbon-rich laminated mudstone, dark-gray laminated mudstone, light-gray massive mudstone, and red massive mudstone. Diagenesis, tectonic compression, off-loading, and weathering have altered the rocks to give some strata greater hydraulic conductivity than other strata. Each stratum in the Lockatong Formation is 0.3 to 8 m thick, strikes N65 degrees E, and dips 25 degrees to 70 degrees NW. The black, carbon-rich laminated mudstone tends to fracture easily, has a relatively high hydraulic conductivity and is associated with high natural gamma-ray count rates. The dark-gray laminated mudstone is less fractured and has a lower hydraulic conductivity than the black carbon-rich laminated mudstone. The light-gray and the red massive mudstones are highly indurated and tend to have the least fractures and a low hydraulic conductivity. The differences in gamma-ray count rates for different mudstones allow gamma-ray logs to be used to correlate and delineate the lithostratigraphy from multiple wells. Gamma-ray logs and rock cores were correlated to develop a 13-layer gamma-ray stratigraphy and 41-layer lithostratigraphy throughout the fractured sedimentary rock research site. Detailed hydrogeologic framework shows that black carbon-rich laminated mudstones are the most hydraulically conductive. Water-quality and aquifer-test data indicate that groundwater flow is greatest and TCE contamination is highest in the black, carbon- and clay-rich laminated mudstones. Large-scale groundwater flow at the NAWC research site can be modeled as highly anisotropic with the highest component of permeability occurring along bedding planes.
Lithium and carbon isotopes in river catchment: combined tracers to constrain chemical weathering processes

NASA Astrophysics Data System (ADS)

Rad, S.; Rive, K.; Assayag, N.; Dictor, M.; Garcin, M.

2012-12-01

Water-rock interactions produced in river catchment are accompanied by fractionation or changes in stable isotopes such as H, Li, C and O during chemical weathering processes. Li is a fluid-mobile element that tends to preferentially partition into the fluid phase during water-rock interaction. The relative mass difference between the two isotopes is considerable, generating large mass dependent fractionation during chemical weathering processes. The CO2 dissolves into the water providing the main acid that attack the rock during chemical weathering. Carbon stable isotopes and concentration of Dissolved Inorganic Carbon (DIC) in the river catchment can be used to determine the origin and consumption rates of CO2. In the present work, stable isotopes were analyzed in Allier River, one of the major river basins of France. The lithology is dominated by granite rocks within current upstream, while it is mainly basaltic and Oligocene sediments in the downstream with hydrothermal manifestations. We propose a new isotopic approach by combining δ7Li and δ13CDIC analyses in river catchment waters. A first method has been applied to volcanic tropical environments with Li concentrations correlated to δ13CDIC (Rad et al., 2011). Here, we have completed this approach by lithium isotopes. Water samples were collected during several field trips. Our results show a large variation in Li isotopes and C isotopes within the catchment from 3.3 ‰ to 30.3 ‰ and from -17.9‰ to -3.5‰, respectively. Chemical weathering rates linearly increase from upstream to downstream over 400km distance, whereas Li isotope signatures decrease and global C signature increases. This is due to low water-rock interaction dominated in upstream, whereas the downstream is punctually impacted by hydrothermalism. From Li and C isotopes, our results show 4 groups reflecting different chemical weathering processes: the first group with high fractionation of Li and C, for Li, the heavy lithium partitioned into surface waters, leaving lighter lithium behind in the weathered products, the signature of C is mainly due to organic matter or partially due to biochemical interaction with assimilation of CO2 by microorganism. The second group involves atmospheric equilibrium with CO2 degassing with organic origin or "cold" CO2 degassing with important fraction of Li. The third group present high fractionation of C, reflecting presence of superficial C with organic origin, with low fractionation of Li underling the hydrothermalism impact. Finally a fourth group with low fractionation mainly due to high temperature water-rock interaction. Therefore, the combination of the two tracers, Li and C isotopes, offers a powerful tool to discriminate chemical weathering processes from sources of alteration during water-rock interactions under multi-lithology terrains. Reference: Rad, S., Rivé, K., Allègre, C.J., 2011. Weathering regime associated with subsurface circulation on volcanic islands. Aquat. Geochem. 17, 3, 221-241.
Deformation associated to exhumation by detachment faulting of upper mantle rocks in a fossil Ocean Continent Transition: The example of the Totalp unit in SE Switzerland

NASA Astrophysics Data System (ADS)

Picazo, S.; Manatschal, G.; Cannat, M.

2013-12-01

The exhumation of upper mantle rocks along detachment faults is widespread at Mid-Ocean Ridges and at the Ocean-Continent Transition (OCT) of rifted continental margins. Thermo-mechanical models indicate that significant strain softening of the fault rocks in the footwall is required in order to produce such large fault offsets. Our work focuses on deformation textures, and the associated mineralogy in ultramafic rocks sampled in the upper levels of the footwall next to the exhumation fault. We present two OCT examples, the Totalp relict of a paleo-Tethys OCT exposed in SE Switzerland, and the Iberian distal margin (ODP Leg 173 Site 1070). We built a new geological map and a section of the Totalp unit near Davos (SE Switzerland) and interpreted this area as a local exposure of a paleo-seafloor that is formed by an exhumed detachment surface and serpentinized peridotites. The top of the exhumed mantle rocks is made of ophicalcites that resulted from the carbonation of serpentine under static conditions at the seafloor. The ophicalcites preserve depositional contacts with Upper Jurassic to Lower Cretaceous pelagic sediments. These sequences did not exceed prehnite-pumpellyite metamorphic facies conditions, and locally escaped Alpine deformation. Thin mylonitic shear zones as well as foliated amphibole-bearing ultramafic rocks have been mapped. The age of these rocks and the link with the final exhumation history are yet unknown but since amphibole-bearing ultramafic rocks can be found as clasts in cataclasites related to the detachment fault, they pre-date detachment faulting. Our petrostructural study of the exhumed serpentinized rocks also reveals a deformation gradient from cataclasis to gouge formation within 150m in the footwall of the proposed paleo-detachment fault. This deformation postdates serpentinization. It involves a component of plastic deformation of serpentine in the most highly strained intervals that has suffered pronounced grain-size reduction and a polyphase cataclastic overprint.
Carbon storage potential in Pleistocene volcanic rocks of the Magnesia area (Central Greece)

NASA Astrophysics Data System (ADS)

Koutsovitis, Petros; Koukouzas, Nikolaos; Magganas, Andreas

2017-04-01

The Porfyrio and Mikrothives volcanoes in the Magnesia area (SE Thessaly, Central Greece) are located a few km (˜8 and 12 km respectively) south-southwest of the industrial area of Volos city and are relatively small in size (˜3 and 10 km2 respectively). They are closely associated with other scattered volcanic centers of Late-Pleistocene-Quaternary age, appearing at the western shores of Pagasitikos gulf and at the Northern Euboikos gulf (e.g. Achilleion, Lichades, Agios Ioannis). This volcanic activity is attributed to back-arc extensional volcanism and may be further associated with propagation tectonics of the North Anatolian fault [1,2,3]. Volcanic rocks from the Porfyrio and Mikrothives mostly consist of basaltic and trachyandesitic lavas and pyroclastic tuffs. Porous basaltic lavas (10-15% porosity) exhibit porphyritic textures with a holocrystalline trachytic groundmass. The groundmass consists of lath-shaped plagioclase crystals, alkali feldspar, clinopyroxene, olivine, oxide minerals (ilmenite, titanomagnetite and magnetite), along with other accessory minerals such as quartz, calcite, apatite and pyrite. Phenocrysts are mostly subhedral and anhedral clinopyroxene crystals (mostly augite and less often diopside), olivine and less often plagioclase and quartz. Cr-spinel crystals have been identified within olivine phenocrysts. Pyroclastic tuffs exhibit vesicular textures, with their porosity varying between 20 and 40%. Their groundmass is hypocrystalline vesicular being either trachytic or aphanitic, often enriched in oxide minerals. Phenocrysts are less frequent compared to the lava samples, most often being feldspars. In some samples, pores are partially filled with secondary calcite. From recent literature it is well known that CO2 can be injected, trapped and retained within the pore spaces of volcanic rocks, forming chemically stable carbonate minerals [4,5,6,7]. The Porfyrio and Mikrothives volcanics can be considered as potential sites for applying in situ and under certain preconditions ex situ [8] geologic carbon capture and storage (CCS) practices. This is due to the textural properties of the volcanic and pyroclastic rocks that are characterized by their high porosity, the chemistry of the rocks, as they contain rather high amounts of Ca, Mg, Fe - the necessary chemical constituents for forming stable carbonate minerals, but also because of the relatively short distance of the outcrop of the rocks with the industrial area of Volos city. It should be noted some of the studied samples already incorporate calcite within the pores, demonstrating the capability of these rocks for CCS applications. An estimated amount of about 3 tons of CO2, dissolved in water, could be stored in the frames of a small pilot project either in the Porfyrio or the Mikrothives volcanics, considering that the average porosity of these volcanics is about 20%. CO2 storage could be possibly applied at a depth greater than 400 meters below the surface, occupying a minimum area of about 104 m3 [cf. 7]. References. [1] Fytikas et al. 1984: Geol Soc London Sp Publ 17, 687-699; [2] Pe-Piper and Piper 2007: Geol Soc Am Sp Pap 418, 17-31; [3] Innocenti et al. 2010: Journal Geol Soc London 167, 475-489; [4] Rochelle, et al. 2004: Geol Soc London Sp Publ 233, 87-106; [5] Rosenbauer et al. 2012: Geoch et Cosmoch Acta 89, 116-133; [6] Matter, et al., 2007: Geochem. Geophys. Geosyst. 8; [7] Matter, et al., 2016: Science 352, 1312-1314.; [8] Rigopoulos et al. 2016: Journal CO2 Utilization 16, 361-370.
Layers with Carbonate Content Inside McLaughlin Crater on Mars

NASA Image and Video Library

2013-01-20

This view of layered rocks on the floor of McLaughlin Crater shows sedimentary rocks that contain spectroscopic evidence for minerals formed through interaction with water. A combination of clues suggests this crater once held a lake fed by groundwater.
Water and carbon in rusty lunar rock 66095

USGS Publications Warehouse

Friedman, I.; Hardcastle, Kenneth G.; Gleason, J.D.

1974-01-01

Lunar rock 66095 contains a hydrated iron oxide and has an unusual amount of water for a lunar rock (140 to 750 parts per million), 90 percent of which is released below 690??C. The ??D of water released at these low temperatures varies from -75 to -140 per mil relative to standard mean ocean water (SMOW). The small amount of water released between 690?? and 1300??C has a ??D of about -175 ?? 25 per mil SMOW. These ??D values are not unusual for terrestrial water. The ??18O of water extracted from 110?? to 400??C has a value of + 5 ?? 1 per mil SMOW, similar to the value for lunar silicates from rock 66095 and different from the value of -4 to -22 per mil found for samples of terrestrial rust including samples of rusted meteoritic iron. The amount of carbon varies from 11 to 59 parts per million with a ??13C from -20 to -30 per mil relative to Pee Dee belemnite. Only very small amounts of reduced species (such as hydrogen, carbon monoxide, and methane) were found, in contrast to the analyses of other lunar rocks. Although it is possible that most of the water in the iron oxide (goethite) may be terrestrial in origin or may have exchanged with terrestrial water during sample return and handling, evidence presented herein suggests that this did not happen and that some lunar water may have a ??D that is indistinguishable from that of terrestrial water.

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