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Kiyoto Futa

Publications and source records attributed to Kiyoto Futa.

At least 19 recordsLinked to original sources

Strontium residual salt analyses (SrRSA) and geochemistry of Bakken Formation core samples from Fleckten 1-20, North Dakota

Samples of Bakken Formation core from the Fleckton 1-20 well in Ward County, North Dakota, were analyzed using the Strontium Residual Salt Analysis (SrRSA) method to assess pore-water communication among the upper, middle, and lower sections of the unit by analyzing 87 Sr/ 86 Sr in pore-water salts leached from the core. Major and trace element analyses were also conducted on bulk-rock samples and leachates (Elemental Residual Salt Analysis or ERSA). The middle part of the Bakken Formation, a calcareous and dolomitic siltstone to fine sandstone, is encased between two black shales—the upper and lower sections of the formation. These units are informal and herein named the upper, middle, and lower Bakken members. Strontium isotope measurements and concentration of some solutes in leachates indicate that pore water in the black shale of the upper Bakken member has remained isolated from pore water in the middle Bakken member except for within a few feet immediately near the contact where elemental profiles indicate diffusive mixing. The SrRSA 87 Sr/ 86 Sr values from the middle Bakken member are consistent with produced water collected from 28 wells in Montana and North Dakota. In contrast to the similarity in 87 Sr/ 86 Sr values, ratios of concentrations such as K/Rb, Ca/Sr, Ca/Mg, and Na/Cl are slightly different between the pore-water leachates and produced water values. The differences in K/Rb and Ca/Sr are probably due to selective adsorption of Rb leading to larger K/Rb ratios and minor dissolution of carbonate minerals leading to larger Ca/Sr ratios in the leachates.

Montana, North Dakota, South Dakota

Characterization and origin of brines from the Bakken-Three Forks petroleum system in the Williston Basin, USA

Brine (also referred to as ‘produced water’) samples were collected from 28 wells producing oil from the Late Devonian-Early Mississippian Bakken and Three Forks Formations in the Williston Basin of eastern Montana and western North Dakota. The samples were analyzed for major ions, trace metals, stable isotopes, and strontium isotopes. The brines in these formations are highly saline with total dissolved solids averaging 308 g/L, almost ten times the salinity of modern seawater. Relative to modern seawater, the brines are enriched approximately 10 to 20 times in [Na], [K], [Cl], and [Br]. Greater enrichments of 100 to 400 times in [Li], [B], [Sr] and [Rb], and 2,000 to 10,000 times in [Cs] and [Ba] are probably due to water-rock interaction (WRI). WRI is further indicated by 87Sr/86Sr values typically between 0.710 and 0.711—considerably larger than marine values of 0.7081 to 0.7083 during this depositional interval. Bakken Formation sediments were deposited in a stratified water column with salinity increasing with depth. The deeper water may have been saturated in calcium carbonate and possibly gypsum, but there is no evidence that halite saturation had been attained. Therefore, brines may have been introduced into the Bakken Formation from the underlying Devonian Prairie Formation or from the overlying Charles Formation before these brines were diluted or replaced by meteoric water. Alternatively, salinity of the native pore water was increased by membrane filtration driven by overpressuring within the Bakken Formation.

Mountain Geologist

A geochemical approach to determine sources and movement of saline groundwater in a coastal aquifer

Geochemical evaluation of the sources and movement of saline groundwater in coastal aquifers can aid in the initial mapping of the subsurface when geological information is unavailable. Chloride concentrations of groundwater in a coastal aquifer near San Diego, California, range from about 57 to 39,400 mg/L. On the basis of relative proportions of major-ions, the chemical composition is classified as Na-Ca-Cl-SO 4 , Na-Cl, or Na-Ca-Cl type water. δ 2 H and δ 18 O values range from −47.7‰ to −12.8‰ and from −7.0‰ to −1.2‰, respectively. The isotopically depleted groundwater occurs in the deeper part of the coastal aquifer, and the isotopically enriched groundwater occurs in zones of sea water intrusion. 87 Sr/ 86 Sr ratios range from about 0.7050 to 0.7090, and differ between shallower and deeper flow paths in the coastal aquifer. 3 H and 14 C analyses indicate that most of the groundwater was recharged many thousands of years ago. The analysis of multiple chemical and isotopic tracers indicates that the sources and movement of saline groundwater in the San Diego coastal aquifer are dominated by: (1) recharge of local precipitation in relatively shallow parts of the flow system; (2) regional flow of recharge of higher-elevation precipitation along deep flow paths that freshen a previously saline aquifer; and (3) intrusion of sea water that entered the aquifer primarily during premodern times. Two northwest-to-southeast trending sections show the spatial distribution of the different geochemical groups and suggest the subsurface in the coastal aquifer can be separated into two predominant hydrostratigraphic layers.

California

Lower-crustal xenoliths from Jurassic kimberlite diatremes, upper Michigan (USA): Evidence for Proterozoic orogenesis and plume magmatism in the lower crust of the southern Superior Province

Jurassic kimberlites in the southern Superior Province in northern Michigan contain a variety of possible lower-crustal xenoliths, including mafic garnet granulites, rare garnet-free granulites, amphibolites and eclogites. Whole-rock major-element data for the granulites suggest affinities with tholeiitic basalts. P–T estimates for granulites indicate peak temperatures of 690–730°C and pressures of 9–12 kbar, consistent with seismic estimates of crustal thickness in the region. The granulites can be divided into two groups based on trace-element characteristics. Group 1 granulites have trace-element signatures similar to average Archean lower crust; they are light rare earth element (LREE)-enriched, with high La/Nb ratios and positive Pb anomalies. Most plot to the left of the geochron on a 206 Pb/ €204 Pb vs 207 Pb/ €204 Pb diagram, and there was probably widespread incorporation of Proterozoic to Archean components into the magmatic protoliths of these rocks. Although the age of the Group 1 granulites is not well constrained, their protoliths appear to be have been emplaced during the Mesoproterozoic and to be older than those for Group 2 granulites. Group 2 granulites are also LREE-enriched, but have strong positive Nb and Ta anomalies and low La/Nb ratios, suggesting intraplate magmatic affinities. They have trace-element characteristics similar to those of some Mid-Continent Rift (Keweenawan) basalts. They yield a Sm–Nd whole-rock errorchron age of 1046 ± 140 Ma, similar to that of Mid-Continent Rift plume magmatism. These granulites have unusually radiogenic Pb isotope compositions that plot above the 207 Pb/ €204 Pb vs 206 Pb/ €204 Pb growth curve and to the right of the 4·55 Ga geochron, and closely resemble the Pb isotope array defined by Mid-Continent Rift basalts. These Pb isotope data indicate that ancient continental lower crust is not uniformly depleted in U (and Th) relative to Pb. One granulite xenolith, S69-5, contains quartz, and has a unique peraluminous composition. It has the lowest εNd and εHf values of the suite. Its isotopic compositions indicate that it is significantly older than the other granulites. Broken zircon cores encased by younger overgrowths suggest that this granulite includes a large component of pre-existing sedimentary rocks. Two distinct populations of zircons from S69-5 were dated by sensitive high-resolution ion microprobe. Abundant rounded zircons yield ages of 1104 ± 42 (2σ) Ma, which coincide with the Mid-Continent Rift flood basalt eruptions. Their morphology is similar to those found in lower-crustal rocks that have undergone granulite-facies metamorphism and thus they are considered to represent the age of Group 2 granulites. Also present are less abundant elongate zircon grains that yield a mean age of 1387 ± 32 (2σ) Ma. Their elongate shapes indicate growth from a melt or fluid, possibly associated with 1·3–1·5 Ga anorogenic granite magmatism exposed in the shallow crust to the south in Wisconsin, or related to an initial encroachment of the Keweenawan plume upon the lower crust. Older ages recognized in zircon cores are less well constrained but may be related to tectono-magmatic events in the southern Superior craton. Within the studied suite only S69-5 was recognized as a remnant of the Late Archean lower crust into which the Group 1 and 2 mafic granulite precursor basalts were intruded. Collectively, the data show that the lower crust beneath northern Michigan formed in Archean times and underwent a variety of tectono-magmatic processes throughout the Proterozoic, including orogenesis, partial melting and mafic magmatic underplating in response to upwelling mantle plumes.

Michigan

Strontium isotope systematics of mixing groundwater and oil-field brine at Goose Lake in northeastern Montana, USA

Groundwater, surface water, and soil in the Goose Lake oil field in northeastern Montana have been affected by Cl − -rich oil-field brines during long-term petroleum production. Ongoing multidisciplinary geochemical and geophysical studies have identified the degree and local extent of interaction between brine and groundwater. Fourteen samples representing groundwater, surface water, and brine were collected for Sr isotope analyses to evaluate the usefulness of 87 Sr/ 86 Sr in detecting small amounts of brine. Differences in Sr concentrations and 87 Sr/ 86 Sr are optimal at this site for the experiment. Strontium concentrations range from 0.13 to 36.9 mg/L, and corresponding 87 Sr/ 86 Sr values range from 0.71097 to 0.70828. The local brine has 168 mg/L Sr and a 87 Sr/ 86 Sr value of 0.70802. Mixing relationships are evident in the data set and illustrate the sensitivity of Sr in detecting small amounts of brine in groundwater. The location of data points on a Sr isotope-concentration plot is readily explained by an evaporation-mixing model. The model is supported by the variation in concentrations of most of the other solutes.

Montana

Assessing the natural performance of felsic tuffs using the Rb-Sr and Sm-Nd systems-A study of the altered zone in the Topopah Spring Member, Paintbrush Tuff, Yucca Mountain, Nevada

Core samples of the Topopah Spring Member of the Paintbrush Tuff from drill hole UE25A#1 were analyzed for Sr and Nd isotopes and selected minor and trace elements to constrain the origin of a zcolitized zone associated with the lower vitrophyre. The Sm-Nd radiogenic isotope system was unperturbed by the alteration, but the Rb-Sr system was severely disturbed in the altered zone. The thick, densely welded high-silica rhyolite is remarkably uniform in composition with only a slight decrease in initial 87 Sr/ 86 Sr ratios with depth (0.7129–0.7125). Quartz latite in the upper part of the Topopah Spring has significantly lower initial Sr isotope ratios (0.7095–0.7114). Locally in the altered zone, Sr and Ca were gained in substantial amounts, and K, Rb, and Y were removed. Ti, Zr, Nb, Ba, La, Ce, Sm, and Nd were relatively immobile during the alteration. Sr added to the altered zone had an isotopic composition of 0.7119 ± 0.0002 and was probably derived from dissolution of glass in the bulk Topopah Spring (high silica rhyolite + quartz latite) and transported downward by infiltration.

Nevada

Strontium isotope detection of brine contamination in the East Poplar oil field, Montana

Brine contamination of groundwater in the East Poplar oil field was first documented in the mid-1980s by the U.S. Geological Survey by using hydrochemistry, with an emphasis on chloride (Cl) and total dissolved solids concentrations. Supply wells for the City of Poplar are located downgradient from the oil field, are completed in the same shallow aquifers that are documented as contaminated, and therefore are potentially at risk of being contaminated. In cooperation with the Office of Environmental Protection of the Fort Peck Tribes, groundwater samples were collected in 2009 and 2010 from supply wells, monitor wells, and the Poplar River for analyses of major and trace elements, including strontium (Sr) concentrations and isotopic compositions. The ratio of strontium-87 to strontium-86 ( 87 Sr/ 86 Sr) is used extensively as a natural tracer in groundwater to detect mixing among waters from different sources and to study the effects of water/rock interaction. On a plot of the reciprocal strontium concentration against the 87 Sr/ 86 Sr ratio, mixtures of two end members will produce a linear array. Using this plotting method, data for samples from most of the wells, including the City of Poplar wells, define an array with reciprocal strontium values ranging from 0.08 to 4.15 and 87 Sr/ 86 Sr ratios ranging from 0.70811 to 0.70828. This array is composed of a brine end member with an average 87 Sr/ 86 Sr of 0.70822, strontium concentrations in excess of 12.5 milligrams per liter (mg/L), and chloride concentrations exceeding 8,000 mg/L mixing with uncontaminated water similar to that in USGS06-08 with 18.0 mg/L chloride, 0.24 mg/L strontium, and a 87 Sr/ 86 Sr ratio of 0.70811. The position of samples from the City of Poplar public-water supply wells within this array indicates that brine contamination has reached all three wells. Outliers from this array are EPU-4G (groundwater from the Cretaceous Judith River Formation), brine samples from disposal wells (Huber 5-D and EPU 1-D), USGS92-11 (a well with water that was considerably contaminated in 1992 and becoming less saline with time), and PNR-27 (only slightly below the defined trend with an 87 Sr/ 86 Sr ratio of 0.70793). Water samples from the City of Poplar wells are also enriched in anions and cations that are abundant in oil-field brine.

Open-File Report

Strontium isotope evolution of pore water and calcite in the Topopah Spring Tuff, Yucca Mountain, Nevada

Yucca Mountain, a ridge of Miocene volcanic rocks in southwest Nevada, is being characterized as a site for a potential high-level radioactive waste repository. One issue of concern for the future performance of the potential repository is the movement of water in and around the potential repository horizon. Past water movement in this unsaturated zone is indicated by fluid inclusions trapped in calcite coatings on fracture footwall surfaces and in some lithophysal cavities. Some of the fluid inclusions have homogenization temperatures above the present-day geotherm (J.F. Whelan, written communication), so determining the ages of the calcite associated with those fluid inclusions is important in understanding the thermal history of the potential repository site. Calcite ages have been constrained by uranium-lead dating of silica polymorphs (opal and chalcedony) that are present in most coatings. The opal and chalcedony ages indicate that deposition of the calcite and opal coatings in the welded part of the Topopah Spring Tuff (TSw hydrogeologic unit) spanned nearly the entire history of the 12.8-million-year-old rock mass at fairly uniform overall long-term rates of deposition (within a factor of five). Constraining the age of a layer of calcite associated with specific fluid inclusions is complicated. Calcite is commonly bladed with complex textural relations, and datable opal or chalcedony may be millions of years older or younger than the calcite layer or may be absent from the coating entirely. Therefore, a more direct method of dating the calcite is presented in this paper by developing a model for strontium evolution in pore water in the TSw as recorded by the strontium coprecipitated with calcium in the calcite. Although the water that precipitated the calcite in fractures and cavities may not have been in local isotopic equilibrium with the pore water, the strontium isotope composition of all water in the TSw is primarily controlled by water-rock interaction in the overlying nonwelded and essentially unfractured Paintbrush Group tuffs (PTn). The method of dating secondary minerals from known strontium evolution rates in rocks cannot be used in this study because it assumes the water that deposited the minerals was in isotopic equilibrium with the rock, which is not the case for the pore water in the TSw. Therefore, the evolution of the strontium isotope composition of the water that deposited the calcite, as recorded by the strontium coprecipitated with calcium in the calcite, was used to develop a model for determining the age of the calcite.

Nevada

Hydrologic inferences from strontium isotopes in pore water from the unsaturated zone at Yucca Mountain, Nevada

Calcite is ubiquitous at Yucca Mountain, occurring in the soils and as fracture and cavity coatings within the volcanic tuff section. Strontium is a trace element in calcite, generally at the tens to hundreds of ppm level. Because calcite contains very little rubidium and the half-life of the 87 Rb parent is billions of years, the 87 Sr/ 86 Sr ratios of the calcite record the ratio in the water from which the calcite precipitated. Dissolution and reprecipitation does not alter these compositions so that, in the absence of other sources of strontium, one would expect the strontium ratios along a flow path to preserve variations inherited from strontium in the soil zone. Strontium isotope compositions of calcites from various settings in the Yucca Mountain region have contributed to the understanding of the unsaturated zone (UZ), especially in distinguishing unsaturated zone calcite from saturated zone calcite. Different populations of calcite have been compared, either to group them together or distinguish them from each other in terms of their strontium isotope compositions. Ground water and perched water have also been analyzed; this paper presents strontium isotope data obtained on pore water.

Nevada

Petrochemistry, age and isotopic composition of alkali basalts from Ponape Island, Western Pacific

Eleven analyzed lava samples from Ponape Island are alkali olivine basalt, basanite and basanitoid. Most lavas are aphyric or sparsely phyric (< 10% phenocrysts) and have phenocrysts of olivine (Fo77-80), clinopyroxene and titanomagnetite, and microphenocrysts of plagioclase (An53-68) in a fine-grained groundmass of olivine, clinopyroxene, plagioclase, opaques, potassic oligoclase, ?? nepheline and accessary phases. Oxygen isotope and Fe2O3 FeO data suggest that most samples are fresh, although H2O contents are high. Xenoliths of chromite-bearing harzburgites and dunites, both with cumulate textures occur in one locality. Major- and trace-element concentrations are similar to other oceanic volcanic islands. Most major elements and compatible trace elements vary systematically with respect to the Mg number [ 100Mg (Mg + Fe2+)]. In contrast, the incompatible trace elements do not correlate with the Mg number, but do covary with other incompatible elements. Simple closed-system shallow fractionation cannot be invoked to explain the observed chemical variation in the lavas. Derivation of the fractionated lavas (Mg number = 66-48) probably involved polybaric crystal fractionation from a high-Mg-number parental liquid. In addition, variable-source concentration of a trace-element-rich minor phase is postulated. However, the mantle was homogeneous with respect to the ratio of 87Sr 86Sr. New KAr age data are not consistent with the hypothesis that Ponape and the Caroline Ridge represent a simple "hot spot". ?? 1984.

Chemical Geology

Chemical and isotopic diversity in basalts dredged from the East Pacific Rise at 10°S, the fossil Galapagos Rise and the Nazca plate

We present petrographic, chemical and isotopic data for fresh lava samples dredged from three regions: (1) the fossil Galapagos Rise; (2) an elongate volcano near this extinct spreading center; and (3) the East Pacific Rise at 10&deg;S. The samples from the Galapagos Rise are among the first samples from any fossil spreading center to be analyzed. Alkalic picrites from the elongate seamount and transitional basalts from the East Pacific Rise are both somewhat unusual rock types considering their respective tectonic environments. The dredges from the East Pacific Rise at about 10&deg;S recovered unusual transitional, light rare-earth element (LREE) enriched basalts which show a range of fractionation. On the basis of their chemical and isotopic abundances, it is unlikely that the lavas are related by a single simple process of magmatic differentiation. We suggest that the mantle source region of these basalts was chemically and isotopically heterogeneous. The chemistry of LREE-depleted tholeiitic basalt dredged from near the axis of the extinct Galapagos Rise indicates complex petrogenesis and differentiation. The presence of tholeiitic basalts here indicates that unlike the Guadalupe and Mathematician fossil ridges, the Galapagos Rise has not been the site of voluminous post-abandonment alkalic volcanism. Alkalic basalts of picritic bulk composition dredged from an elongate seamount near the Galapagos Rise do not represent liquid compositions. Instead, we suggest that these alkalic liquids contain added olivine and plagioclase xenocrysts. Although most of the samples analyzed are very fresh, a few have been altered. The latter exhibit characteristic chemical and isotopic effects of seawater alteration.

Marine Geology