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Z. E. Peterman

Publications and source records attributed to Z. E. Peterman.

At least 19 recordsLinked to original sources
USGS2010

Crustal-scale thrusting and origin of the Montreal River monocline-A 35-km-thick cross section of the midcontinent rift in northern Michigan and Wisconsin

A structurally simple, 35-km-thick, north facing stratigraphic succession of Late Archean to Middle Proterozoic rocks is exposed near the Montreal River, which forms the border between northern Wisconsin and Michigan. This structure, the Montreal River monocline, is composed of steeply dipping to vertical sedimentary rocks and flood basalts of the Keweenawan Supergroup (Middle Proterozoic) along the south limb of the Midcontinent rift, and disconformably underlying sedimentary rocks of the Marquette Range Supergroup (Early Proterozoic). These rocks lie on an Archean granite-greenstone complex, about 10 km of which is included in the monocline. This remarkable thickness of rocks appears to be essentially structurally intact and lacks evidence of tectonic thickening or repetition. Tilting to form the monocline resulted from southward thrusting on listric faults of crustal dimension. The faults responsible for the monocline are newly recognized components of a well-known regional fault system that partly closed and inverted the Midcontinent rift system. Resetting of biotite ages on the upper plate of the faults indicates that faulting and uplift occurred at about 1060 +/−20 Ma and followed very shortly after extension that formed the Midcontinent rift system.

Tectonics↗
USGS2010

The Goodman swell: A lithospheric flexure caused by crustal loading along the midcontinent rift system

Rb-Sr biotite ages of Archean and Early to Middle Proterozoic crystalline rocks in northern Wisconsin and adjacent Upper Peninsula of Michigan describe a regionally systematic pattern related to differential uplift. An “age low” occurs in northern Wisconsin where values range from 1070–1172 Ma for rocks with crystallization ages of 1760 to 1865 Ma. These values overlap with the main episode of mafic igneous activity (1090 to 1120 Ma) along the Midcontinent rift system (MRS). We interpret these low biotite ages as registering closure due to cooling below the 300°C isotherm as a consequence of uplift and rapid erosion of an area that we are informally naming the Goodman swell. The position of the Goodman swell is independent of the Archean and Early Proterozoic regional geologic framework but closely linked with the curvilinear (concave to the south) MRS. We interpret the swell to be a forebulge imposed on an elastic crust by loading of mafic igneous rocks along and within the axis of the MRS. The southward concavity of load axes resulted in flexural interaction that localized the swell. Because of rapid uplift the swell may have been a source area for clastic sediments in the rift sequence.

Lake Superior↗
USGS2007

Geochemistry of natural components in the near-field environment, Yucca Mountain, Nevada

The natural near-field environment in and around the emplacement drifts of the proposed nuclear waste repository at Yucca Mountain, Nevada, includes the host rock, dust, seepage, and pore water. The chemical compositions of these components have been determined for assessing possible chemical and mineralogical reactions that may occur after nuclear waste is emplaced. The rock hosting the proposed repository is relatively uniform as shown by a mean coefficient of variation (CV) of 9 percent for major elements. In contrast, compositional variations of dust (bulk and water-soluble fractions), pore water, and seepage are large with mean CVs ranging from 28 to 64 percent. ?? 2007 Materials Research Society.

Conference Paper↗
USGS2006

Evidence for ground-water stratification near Yucca Mountain, Nevada

Major- and trace-element concentrations and strontium isotope ratios (strontium-87/strontium-86) in samples of ground water potentially can be useful in delineating flow paths in the complex ground-water system in the vicinity of Yucca Mountain, Nevada. Water samples were collected from boreholes to characterize the lateral and vertical variability in the composition of water in the saturated zone. Discrete sampling of water-producing intervals in the saturated zone includes isolating borehole sections with packers and extracting pore water from core obtained by sonic drilling. Chemical and isotopic stratification was identified in the saturated zone beneath southern Fortymile Wash.

Conference Paper↗
USGS2005

Geochemical and C, O, Sr, and U-series isotopic evidence for the meteoric origin of calcrete at Solitario Wash, Crater Flat, Nevada, USA

Calcite-rich soils (calcrete) in alluvium and colluvium at Solitario Wash, Crater Flat, Nevada, USA, contain pedogenic calcite and opaline silica similar to soils present elsewhere in the semi-arid southwestern United States. Nevertheless, a ground-water discharge origin for the Solitario Wash soil deposits was proposed in a series of publications proposing elevation-dependent variations of carbon and oxygen isotopes in calcrete samples. Discharge of ground water in the past would raise the possibility of future flooding in the unsaturated zone at Yucca Mountain, Nevada, site of a proposed high-level nuclear waste repository. New geochemical and carbon, oxygen, strontium, and uranium-series isotopic data disprove the presence of systematic elevation-isotopic composition relations, which are the main justification given for a proposed ground-water discharge origin of the calcrete deposits at Solitario Wash. Values of ??13C (-4.1 to -7.8 per mil [???]), ??18O (23.8-17.2???), 87Sr/ 86Sr (0.71270-0.71146), and initial 234U/238U activity ratios of about 1.6 in the new calcrete samples are within ranges previously observed in pedogenic carbonate deposits at Yucca Mountain and are incompatible with a ground-water origin for the calcrete. Variations in carbon and oxygen isotopes in Solitario Wash calcrete likely are caused by pedogenic deposition from meteoric water under varying Quaternary climatic conditions over hundreds of thousands of years. ?? Springer-Verlag 2005.

Environmental Geology↗
USGS2003

Chemical analyses of pore water from boreholes USW SD-6 and USW WT-24, Yucca Mountain, Nevada

Analyses of pore water extracted from cores of boreholes USW SD-6 in the central part and USW WT-24 in the northern part of Yucca Mountain, Nevada, show significant vertical and lateral variations in dissolved-ion concentrations. Analyses of samples of only a few milliliters of pore water extracted by uniaxial or triaxial compression and by ultracentrifugation methods from adjacent core samples are generally in agreement, within the analytical error of 10% to 15%. However, the values of silica for water obtained by ultracentrifugation are consistently lower than values for water obtained by compression. The larger concentrations probably are due to localized pressure solution of silicate minerals during compression. The shallower water from core in borehole USW SD-6 was extracted from nonwelded units collectively referred to as the Paintbrush Tuff nonwelded (PTn). The deeper water was from core in both boreholes USW SD-6 and USW WT-24 in the nonwelded units referred to as the Calico Hills nonwelded (CHn). Significant differences in mean dissolved-ion concentrations in pore water between the PTn and CHn are (1) decreases in Ca, Mg, SO4, and NO3 and (2) increases in HCO3 and (Na+K)/(Ca+Mg) ratios. The decrease in NO3 and the increase in HCO3 could be the result of denitrification through the oxidation of organic matter. The decrease in Ca and associated increase in (Na+K)/(Ca+Mg) is the result of ion exchange with zeolites in the CHn in borehole USW WT-24. This effect is not nearly as pronounced in borehole USW SD-6, probably reflecting a smaller amount of zeolitization of the CHn in USW SD-6. Geochemical calculations using the PHREEQC code indicate that the pore water from both boreholes USW SD-6 and USW WT-24 is uniformly undersaturated in anhydrite, gypsum, and amorphous silica, but supersaturated in quartz and chalcedony. The saturation of calcite, aragonite, sepiolite, and dolomite is more variable from sample to sample. ?? 2002 Elsevier Science B.V. All rights reserved.

Journal of Contaminant Hydrology↗
USGS2003

Estimation of past seepage volumes from calcite distribution in the Topopah Spring Tuff, Yucca Mountain, Nevada

Low-temperature calcite and opal record the past seepage of water into open fractures and lithophysal cavities in the unsaturated zone at Yucca Mountain, Nevada, site of a proposed high-level radioactive waste repository. Systematic measurements of calcite and opal coatings in the Exploratory Studies Facility (ESF) tunnel at the proposed repository horizon are used to estimate the volume of calcite at each site of calcite and/or opal deposition. By estimating the volume of water required to precipitate the measured volumes of calcite in the unsaturated zone, seepage rates of 0.005 to 5 liters/year (l/year) are calculated at the median and 95th percentile of the measured volumes, respectively. These seepage rates are at the low end of the range of seepage rates from recent performance assessment (PA) calculations, confirming the conservative nature of the performance assessment. However, the distribution of the calcite and opal coatings indicate that a much larger fraction of the potential waste packages would be contacted by this seepage than is calculated in the performance assessment.

Journal of Contaminant Hydrology↗
USGS2002

Geochemistry of rock units at the potential repository level, Yucca Mountain, Nevada

The compositional variability of the phenocryst-poor member of the 12.8 Ma Topopah Spring Tuff at the potential repository level was assessed by duplicate analysis of 20 core samples from the cross drift at Yucca Mountain, Nevada. Previous analyses of outcrop and core samples of the Topopah Spring Tuff showed that the phenocryst-poor rhyolite, which includes both lithophysal and nonlithophysal zones, is relatively uniform in composition. Analyses of rock samples from the cross drift, the first from the actual potential repository block, also indicate the chemical homogeneity of this unit excluding localized deposits of vapor-phase minerals and low-temperature calcite and opal in fractures, cavities, and faults. The possible influence of vapor-phase minerals and calcite and opal coatings on rock composition at a scale sufficiently large to incorporate these heterogeneously distributed deposits was evaluated and is considered to be relatively minor. Therefore, the composition of the phenocryst-poor member of the Topopah Spring Tuff is considered to be adequately represented by the analyses of samples from the cross drift. The mean composition as represented by the 10 most abundant oxides in wt. % or g/100 g is: SiO2, 76.29; Al2O3, 12.55; FeO, 0.14; Fe2O3, 0.97; MgO, 0.13; CaO, 0.50; Na2O, 3.52; K2O, 4.83; TiO2, 0.11; and MnO, 0.07. ?? 2002 Published by Elsevier Science Ltd.

Applied Geochemistry↗
USGS2002

U-Pb ages of secondary silica at Yucca Mountain, Nevada: Implications for the paleohydrology of the unsaturated zone

Uranium, Th and Pb isotopes were analyzed in layers of opal and chalcedony from individual mm- to cm-thick calcite and silica coatings at Yucca Mountain, Nevada, USA, a site that is being evaluated for a potential high-level nuclear waste repository. These calcite and silica coatings on fractures and in lithophysal cavities in Miocene-age tuffs in the unsaturated zone (UZ) precipitated from descending water and record a long history of percolation through the UZ. Opal and chalcedony have high concentrations of U (10 to 780 ppm) and low concentrations of common Pb as indicated by large values of 206Pb/204Pb (up to 53,806), thus making them suitable for U-Pb age determinations. Interpretations of U-Pb isotope systems in opal samples at Yucca Mountain are complicated by the incorporation of excess 234U at the time of mineral formation, resulting in reverse discordance of U-Pb ages. However, the 207PB/235U ages are much less affected by deviation from initial secular equilibrium and provide reliable ages of most silica deposits between 0.6 and 9.8 Ma. For chalcedony subsamples showing normal age discordance, these ages may represent minimum times of deposition. Typically, 207Pb/235U ages are consistent with the microstratigraphy in the mineral coating samples, such that the youngest ages are for subsamples from outer layers, intermediate ages are from inner layers, and oldest ages are from innermost layers. 234U and 230Th in most silica layers deeper in the coatings are in secular equilibrium with 238U, which is consistent with their old age and closed system behavior during the past -0.5 Ma. The ages for subsamples of silica layers from different microstratigraphic positions in individual calcite and silica coating samples collected from lithophysal cavities in the welded part of the Topopah Spring Tuff yield slow long-term average growth rates of 1 to 5 mm/Ma. These data imply that the deeper parts of the UZ at Yucca Mountain maintained long-term hydrologic stability over the past 10 Ma. despite significant climate variations. U-Pb ages for subsamples of silica layers from different microstratigraphic positions in individual calcite and silica coating samples collected from fractures in the shallower part of the UZ (welded part of the overlying Tiva Canyon Tuff) indicate larger long-term average growth rates up to 23 mm/Ma and an absence of recently deposited materials (ages of outermost layers are 3-5 Ma.). These differences between the characteristics of the coatings for samples from the shallower and deeper parts of the UZ may indicate that the nonwelded tuffs (PTn), located between the welded parts of the Tiva Canyon and Topopah Spring Tuffs, play an important role in moderating UZ flow.

Applied Geochemistry↗
USGS2002

Physical and stable-isotope evidence for formation of secondary calcite and silica in the unsaturated zone, Yucca Mountain, Nevada

Calcite and silica form coatings on fracture footwalls and cavity floors in the welded tuffs at Yucca Mountain, the potential site of a high-level radioactive waste repository. These secondary mineral deposits are heterogeneously distributed in the unsaturated zone (UZ) with fewer than 10% of possible depositional sites mineralized. The paragenetic sequence, compiled from deposits throughout the UZ, consists of an early-stage assemblage of calcite??fluorite??zeolites that is frequently capped by chalcedony??quartz. Intermediate- and late-stage deposits consist largely of calcite, commonly with opal on buried growth layers or outermost crystal faces of the calcite. Coatings on steep-dipping fractures usually are thin (??? 3 mm) with low-relief outer surfaces whereas shallow-dipping fractures and lithophysal cavities typically contain thicker, more coarsely crystalline deposits characterized by unusual thin, tabular calcite blades up to several cms in length. These blades may be capped with knobby or corniced overgrowths of late-stage calcite intergrown with opal. The observed textures in the fracture and cavity deposits are consistent with deposition from films of water fingering down fracture footwalls or drawn up faces of growing crystals by surface tension and evaporated at the crystal tips. Fluid inclusion studies have shown that most early-stage and some intermediate-stage calcite formed at temperatures of 35 to 85??C. Calcite deposition during the past several million years appears to have been at temperatures < 30??C. The elevated temperatures indicated by the fluid inclusions are consistent with temperatures estimated from calcite ??18O values. Although others have interpreted the elevated temperatures as evidence of hydrothermal activity and flooding of the tuffs of the potential repository, the authors conclude that the temperatures and fluid-inclusion assemblages are consistent with deposition in a UZ environment that experienced prolonged heat input from gradual cooling of nearby plutons. The physical restriction of the deposits (and, therefore, fluid flow) to fracture footwalls and cavity floors and the heterogeneous and limited distribution of the deposits provides compelling evidence that they do not reflect flooding of the thick UZ at Yucca Mountain. The textures and isotopic and chemical compositions of these mineral deposits are consistent with deposition in a UZ setting from meteoric waters percolating downward along fracture flow paths.

Applied Geochemistry↗
USGS1999

Synopsis of strontium isotope variations in groundwater at Aspo, southern Sweden

Strontium isotope ratios are used to identify end-member ground-water compositions at Aspo in southeastern Sweden where the Hard Rock Laboratory (HRL) has been constructed to evaluate the suitability of crystalline rock for the geologic disposal of nuclear waste. The Hard Rock Laboratory is a decline (tunnel) constructed in 1.8 Ga-old granitic rock that forms islands in an archipelago along the Swedish coast. Ground-water samples were obtained for isotopic analyses from boreholes drilled from the surface and from side boreholes drilled within the HRL. Infiltration at Aspo occurs primarily through fractures zones in the granitic bedrock beneath thin soils throughout the area. Because of extremely low Sr concentrations, rain and snow are not important contributors to the Sr isotope budget of the ground-water system. At shallow levels, water percolating downward along fractures and fracture zones acquires a ??87Sr between +9.5 and +10.0??? and maintains this value downward while Sr concentrations increase by two orders of magnitude. Ground-water samples from both boreholes and from in the HRL show the effects of mixing with saline waters containing as much as 59 mg/L Sr and ??87Sr values as large as +13.92%, Baltic Sea water is a potential component of the groundwater system with ??87Sr values only slightly larger than modern marine values (+0.3???) but with much lower concentrations (1.5 mg/L) than ocean water (8 mg/L). However, because of large Sr concentration differences between the saline groundwater (59 mg/L) and Baltic Sea water (1.5 rag/L), ??87Sr values are not particularly sensitive indicators of sea-water intrusion even though their ??87Sr values differ substantially.

Applied Geochemistry↗
USGS1997

Using δ 87 Sr values to identify sources of salinity to a freshwater aquifer, Greater Aneth Oil Field, Utah, USA

Salinity increases in water from the freshwater Navajo aquifer in the Aneth area have been documented in recent years. Previous studies during the 1980s in the Aneth area suggested that brines associated with oil production and their subsequent re-injection were the probable source of salinity in the Navajo aquifer. Differences in the delta strontium-87 (&delta; 87 Sr) composition of ground-water samples from southeastern Utah were used to determine if oil-field brine or water from the upper Paleozoic aquifer is a plausible source of salinity to the Navajo aquifer. The &delta; 87 Sr values of the oil-field brine samples (mean = &minus;0.95%, range = &minus;1.06 to &minus;0.79%, n = 5) are substantially more negative than the values in water samples from wells completed in the Navajo aquifer (mean = 0.73, range = &minus;0.85 to 2.02%, n = 48), indicating that oil-field brine is not a source of salinity. The &delta; 87 Sr values in water samples from wells completed in the upper Paleozoic aquifer (mean = 0.801% range = 0.34 to 1.10%, n = 4) are similar to the mean isotopic composition of the more saline water from the Navajo aquifer. The &delta; 87 Sr values in water from the Navajo aquifer confirm that two distinct flow areas are present. Mixing models using the &delta; 87 Sr values and Sr concentrations of non-saline water from the Navajo aquifer and saline water from the upper Paleozoic aquifer indicate that water from the upper Paleozoic aquifer is a plausible source of saline water to the Navajo aquifer. Most Navajo aquifer wells that contain water with a &delta; 87 Sr signature similar to water from the upper Paleozoic aquifer are located within or adjacent to an area where the hydraulic gradient is favorable for upward movement of water from the upper Paleozoic aquifer into the Navajo aquifer.

Chemical Geology↗
USGS1997

A reconnaissance study of oxygen, hydrogen and strontium isotopes in geochemically diverse lakes, Western Nebraska, USA

Reconnaissance ??18O,, ??D, and ??87Sr data for fifteen lakes in the Western Lakes Region of the Sand Hills of Nebraska indicate dynamic hydrologic systems. The rather narrow range of ??87Sr from lake water (1.1 to 2.1) and groundwater (0.9 to 1.7) indicates that the groundwater is generally unradiogenic. Groundwater residence times and relatively unradiogenic volcanic ash within the dune sediments control the ??87Sr values. Based on the mutual variations of ??18O and ??D, the lakes can be divided into three groups. In Group 1, both ??18O and ??D values increase from spring to fall. The ??18O and ??D values in Group 2 decreased from spring to fall. Group 3 are ephemeral lakes that went dry some time during 1992. The data and isotopic modeling show that variations in the ratio of evaporation relative to groundwater inflow, local humidity conditions, and the ??(a) has substantial influence on the isotopic composition. In addition, isotopic behavior in ephemeral hakes can be rather unusual because of the changing activities of water and mineral precipitation and redissolution. The annual and interannual isotopic variability of these lakes which is reflected in the paleonvironmental indicators may be the rule rather than the exception in these types of systems.

Journal of Paleolimnology↗