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Chemical analyses for the geologic map of the Island of Hawaii
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National Irrigation Water Quality Program data-synthesis data base
Under the National Irrigation Water Quality Program (NIWQP) of the U.S. Department of the Interior, researchers investigated contamination caused by irrigation drainage in 26 areas in the Western United States from 1986 to 1993. From 1992 to 1995, a comprehensive relational data base was built to organize data collected during the 26-area investigations. The data base provided the basis for analysis and synthesis of these data to identify common features of contaminated areas and hence dominant biologic, geologic, climatic, chemical, and physiographic factors that have resulted in contamination of water and biota in irrigated areas in the Western United States. Included in the data base are geologic, hydrologic, climatological, chemical, and cultural data that describe the 26 study areas in 14 Western States. The data base contains information on 1,264 sites from which water and bottom sediment were collected. It also contains chemical data from 6,903 analyses of surface water, 914 analyses of ground water, 707 analyses of inorganic constituents in bottom sediments, 223 analyses of organochlorine pesticides in bottom sediments, 8,217 analyses of inorganic constituents in biota, and 1,088 analyses for organic constituents in biota. The data base is available to the public and can be obtained at the NIWQP homepage http://www.usbr.gov/niwqp as dBase III tables for personal-computer systems or as American Standard Code for Information Exchange structured query language (SQL) command and data files for SQL data bases.
Origin of epigenetic calcite in coal from Antarctica and Ohio based on isotope compositions of oxygen, carbon and strontium
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.
Science in support of the Deepwater Horizon response
This introduction to the Special Feature presents the context for science during the Deepwater Horizon oil spill response, summarizes how scientific knowledge was integrated across disciplines and statutory responsibilities, identifies areas where scientific information was accurate and where it was not, and considers lessons learned and recommendations for future research and response. Scientific information was integrated within and across federal and state agencies, with input from nongovernmental scientists, across a diverse portfolio of needs—stopping the flow of oil, estimating the amount of oil, capturing and recovering the oil, tracking and forecasting surface oil, protecting coastal and oceanic wildlife and habitat, managing fisheries, and protecting the safety of seafood. Disciplines involved included atmospheric, oceanographic, biogeochemical, ecological, health, biological, and chemical sciences, physics, geology, and mechanical and chemical engineering. Platforms ranged from satellites and planes to ships, buoys, gliders, and remotely operated vehicles to laboratories and computer simulations. The unprecedented response effort depended directly on intense and extensive scientific and engineering data, information, and advice. Many valuable lessons were learned that should be applied to future events.
Geochemistry of ground water
The science of geochemistry is the study of the chemical composition of and actual or possible chemical changes in the crust of the earth. The subdivision of geochemistry concerned with ground water includes study of the nature and amounts of dissolved mineral matter in ground waters, the chemical and geologic changes that influence the kinds and amounts of substances carried in solution, and the chemical relationships between dissolved mineral matter in waters and minerals that make up the rocks in which the waters occur. As . thus defined, the field of geochemistry of ground water is very large. Although much work has been done in geochemistry in general, and in some phases of the geochemistry of ground water, the field remains to a large extent unexplored.
Combined ecological and geologic perspectives in ecosystem studies
No abstract available.
U-Pb SHRIMP dating of uraniferous opals
U-Pb and U-series analyses of four U-rich opal samples using sensitive high-resolution ion microprobe (SHRIMP) demonstrate the potential of this technique for the dating of opals with ages ranging from several tens of thousand years to millions of years. The major advantages of the technique, compared to the conventional thermal ionisation mass spectrometry (TIMS), are the high spatial resolution (???20 ??m), the ability to analyse in situ all isotopes required to determine both U-Pb and U-series ages, and a relatively short analysis time which allows obtaining a growth rate of opal as a result of a single SHRIMP session. There are two major limitations to this method, determined by both current level of development of ion probes and understanding of ion sputtering processes. First, sufficient secondary ion beam intensities can only be obtained for opal samples with U concentrations in excess of ???20 ??g/g. However, this restriction still permits dating of a large variety of opals. Second, U-Pb ratios in all analyses drifted with time and were only weakly correlated with changes in other ratios (such as U/UO). This drift, which is difficult to correct for, remains the main factor currently limiting the precision and accuracy of the U-Pb SHRIMP opal ages. Nevertheless, an assumption of similar behaviour of standard and unknown opals under similar analytical conditions allowed successful determination of ages with precisions of ???10% for the samples investigated in this study. SHRIMP-based U-series and U-Pb ages are consistent with TIMS dating results of the same materials and known geological timeframes. ?? 2005 Elsevier B.V. All rights reserved.
The promise of precise borehole gravimetry in petroleum exploration and exploitation
This report provides comprehensive information on the geology, geohydrology, and mineral resources of Boone and Winnebago Counties for use in resource-based land-use planning and development. Data on the composition, thickness, and regional distribution of glacial drift and bedrock materials were used to construct maps of: geologic materials to a depth of 20 ft; bedrock topography; drift thickness; major terrains; and glacial drift aquifers. Because contamination of aquifers is a serious concern in some areas of the two counties, a major focus of this study is on interpreting data critical to the selection of suitable areas for municipal waste disposal and prevention of contamination from existing municipal landfills and septic systems. Interpretive maps accompanying the text: (1) rate geological sequences on their capacity to protect aquifers and surface water from contamination by land burial of municipal wastes, septic system disposal, and surface spreading of wastes and agricultural chemicals; (2) geologic sequences on their suitability for general construction; and (3) delineate resources of sand, gravel, peat, and dolomite. Areas in which aquifer contamination from waste disposal and other land-use practices is most likely to occur are those in which sand and gravel and/or permeable creviced bedrock are at or near the surface. Areas having the lowest contamination potential are underlain by thick (20 ft or more) deposits of fine-grained glacial till. Areas most favorable for general construction are well-drained locations in major river valleys and terrace outwash plains; areas least favorable for construction are scattered throughout both counties on poorly drained land having low bearing capacities and on uplands and slopes in northwestern Winnebago County where the drift is thin over the bedrock. Extensive deposits of sand and gravel occur in the major bedrock valleys. Dolomite deposits underlie all the uplands of Winnebago County and most of Boone County, but extraction costs are prohibitive where overburden is thick. High-grade dolomite with relatively thin overburden is found in eastern Winnebago County and southwestern Boone County. (Author 's abstract)
Distinguishing seawater from geologic brine in saline coastal groundwater using radium-226; an example from the Sabkha of the UAE
Sabkhat (Salt flats) are common geographic features of low-lying marine coastal areas that develop under hyper-arid climatic conditions. They are characterized by the presence of highly concentrated saline solutions and evaporitic minerals, and have been cited in the geologic literature as present-day representations of hyper-arid regional paleohydrogeology, paleoclimatology, coastal processes, and sedimentation in the geologic record. It is therefore important that a correct understanding of the origin and development of these features be achieved. Knowledge of the source of solutes is an important first step in understanding these features. Historically, two theories have been advanced as to the main source of solutes in sabkha brines: an early concept entailing seawater as the obvious source, and a more recent and dynamic theory involving ascending geologic brine forced upward into the base of the sabkha by a regional hydraulic gradient in the underlying formations. Ra-226 could uniquely distinguish between these sources under certain circumstances, as it is typically present at elevated activity of hundreds to thousands of Bq/m 3 (Becquerels per cubic meter) in subsurface formation brines; at exceedingly low activities in open ocean and coastal water; and not significantly supplied to water from recently formed marine sedimentary framework material. The coastal marine sabkha of the Emirate of Abu Dhabi was used to test this hypothesis. The distribution of Ra-226 in 70 samples of sabkha brine (mean: 700 Bq/m 3 ), 7 samples of underlying deeper formation brine (mean: 3416 Bq/m 3 ), the estimated value of seawater (< 16 Bq/m 3 ) and an estimate of supply from sabkha sedimentary framework grains (<~6 Bq/m 3 ) provide the first direct evidence that ascending geologic brine contributes significantly to the solutes of this sabkha system.
Integrating detrital magnetite geochemistry and (U-Th)/He chronometry as a sediment provenance tool in geologic and metallogenic terranes
Magnetite is ubiquitous in porphyry Cu systems and in sediment sourcing both barren and mineralized regions, with potential as an indicator mineral in concealed and coarsely-mapped terranes. We develop and test a workflow for integrated geochemistry and (U–Th)/He (He) dating for inferring detrital magnetite (DMt) provenance in these settings. The ca. 70 Ma Taurus porphyry Cu–Mo(–Au) district in eastern interior Alaska serves as a test case. DMt from streams draining porphyry-related mineralization was characterized by geochemistry and mineral inclusion and microstructure observations, complemented by similar data for potential porphyry and host rock sources. Principal component analysis and clustering of DMt geochemical data resolve multiple populations in our samples geochemically and texturally compatible with derivation from metamorphic, porphyry-related hydrothermal, and igneous sources. Hydrothermal magnetite comprises ∼16–50% of DMt nearest porphyry mineralization but diminishes to ∼4% ∼15 km downstream. Subsampled grains within populations yield ∼160–110 Ma, ∼70 Ma, ∼55 Ma, and ∼20 Ma magnetite He date modes. Combined with provenance, He dates capture Early Cretaceous regional exhumation of metamorphic host rock and Late Cretaceous porphyry Cu mineralization. DMt grains showing partial hematite replacement yield ca. 55–20 Ma dates regardless of source, overlapping regional warm/wet climatic intervals. We interpret Cenozoic dates to reflect exhumation to near-surface oxidizing conditions and(or) supergene weathering. Magnetite is thus a promising target phase for (1) tracking the spatiotemporal distribution of porphyry systems, and (2) linking the formation and exhumation of these systems to a regional geologic history, both in Alaska and globally.
Estuarine Geomorphology, Circulation, and Mixing
To understand the processes affecting the distribution and cycles of particulates, pollutants, nutrients, and organisms in estuaries, it is insufficient to focus solely on the biological and chemical aspects of the processes. Water sources and movements (e.g. evaporation, precipitation, riverine discharge, submarine ground water discharge, wetland hydrology, and tidal exchange) as well as other hydrodynamic aspects of coastal systems, including circulation patterns, stratification, mixing and flushing, must also be considered. When hydrodynamic changes occur quickly relative to biological, geological, and chemical transformations, they become the dominant controlling factors of many ecological processes in estuaries (Officer 1980), and it is now widely recognized that a thorough understanding of the marine estuarine ecology requires comprehensive knowledge and integration of physical processes affecting the system. Using the terminology of a shallow-water oceanographer, this chapter aims to organize, classify, and describe some of these important physical characteristics and processes.
A geochemical study of oil in metalliferous veins, Idarado Mine, San Juan Mountains, Colorado
A tarry, benzene-soluble material is present in metal-rich veins in the Idarado mine, Ouray County, Colo., in an area not known to have petroleum resources. The material was compared chemically, spectometrically, and chromatographically with oils from four fields in the nearby Paradox basin. Each of these oil fields contains reservoir rocks equivalent to rock units known to extend beneath volcanic rocks near the mine. Carbon and sulfur isotope data and gas chromatographic data indicate a similarity between the oil from the nearby Sierra field and the oil from the mine. Thus, it seems both geologically and chemically possible that oil in the mine originated in Cretaceous sediments. Variations in the composition of oil from the mine and differences between the mine oil and Sierra oil, notably in the distributions of hydrocarbons, are attributed to bacterial degradation.
Deciphering fluid sources of hydrothermal systems: A combined Sr- and S-isotope study on barite (Schwarzwald, SW Germany)
Primary and secondary barites from hydrothermal mineralizations in SW Germany were investigated, for the first time, by a combination of strontium (Sr) isotope systematics ( 87 Sr/ 86 Sr), Sr contents and δ 34 S values to distinguish fluid sources and precipitation mechanisms responsible for their formation. Barite of Permian age derived its Sr solely from crystalline basement rocks, whereas all younger barite also incorporate Sr from formation waters of the overlying sediments. In fact, most of the Sr in younger barite is leached from Lower and Middle Triassic sediments. In contrast, most of the sulfur (S) of Permian, Jurassic and northern Schwarzwald Miocene barite originated from basement rocks. The S source of Upper Rhinegraben (URG)-related Paleogene barite differs depending on geographic position: for veins of the southern URG, it is the Oligocene evaporitic sequence, while central URG mineralizations derived its S from Middle Triassic evaporites. Using Sr isotopes of barite of known age combined with estimates on the Sr contents and Sr isotopic ratios of the fluids' source rocks, we were able to quantify mixing ratios of basement-derived fluids and sedimentary formation waters for the first time. These calculations show that Jurassic barite formed by mixing of 75–95% ascending basement-derived fluids with 5–25% sedimentary formation water, but that only 20–55% of the Sr was brought by the basement-derived fluid to the depositional site. Miocene barite formed by mixing of an ascending basement-derived brine (60–70%) with 30–40% sedimentary formation waters. In this case, only 8–15% of the Sr was derived from the deep brine. This fluid-mixing calculation is an example for deposits in which the fluid source is known. This method applied to a greater number of deposits formed at different times and in various geological settings may shed light on more general causes of fluid movement in the Earth's crust and on the formation of hydrothermal ore deposits.
Re-Os dating of paleozoic organic-rich black shales by LA-ICP-MS/MS
We present a new in-situ method for Re- Os geochronology of black shales using LA-ICP-MS/MS that is rapid, cost-effective, and sufficiently accurate and precise to address many geological questions. The method is tested on Paleozoic organic-rich black shales with independently constrained stratigraphic or radiometric ages. Results demonstrate that LA-ICP-MS/MS analysis yields Re- Os dates and initial Os isotopic compositions generally within uncertainty of published values using a laser spot size of 100 to 120 μ m in diameter. Despite low Os abundances in many samples, high-density microscale sampling compensates through large numbers of analyses, enabling robust inverse isochron regressions. The approach also allows contemporaneous acquisition of trace- element data (V, Ni, Mo and Re), providing insight into metal distribution in a sample, degree of metal enrichments, and serve as a proxy for open-system behavior for Re- Os. As a result, LA-ICP-MS/MS Re- Os analysis can serve both as a stand-alone geochronological tool and as an efficient screening method prior to conventional ID-N-TIMS, helping to identify optimal intervals and exclude isotopically disturbed material. Together, our study demonstrates that in-situ Re- Os geochronology of organic-rich shales is technically viable, geologically informative, and broadly applicable, opening new opportunities to investigate basin evolution, metallogenesis, hydrocarbon systems, and Earth-system processes across deep time.
Nitrogen release from rock and soil under simulated field conditions
A laboratory study was performed to simulate field weathering and nitrogen release from bedrock in a setting where geologic nitrogen has been suspected to be a large local source of nitrate. Two rock types containing nitrogen, slate (1370 mg N kg-1) and greenstone (480 mg N kg-1), were used along with saprolite and BC horizon sand from soils derived from these rock types. The fresh rock and weathered material were used in batch reactors that were leached every 30 days over 6 months to simulate a single wet season. Nitrogen was released from rock and soil materials at rates between 10-20 and 10-19 mo1 N cm-2 s-1. Results from the laboratory dissolution experiments were compared to in situ soil solutions and available mineral nitrogen pools from the BC horizon of both soils. Concentrations of mineral nitrogen (NO3- + NH4+) in soil solutions reached the highest levels at the beginning of the rainy season and progressively decreased with increased leaching. This seasonal pattern was repeated for the available mineral nitrogen pool that was extracted using a KCl solution. Estimates based on these laboratory release rates bracket stream water NO3-N fluxes and changes in the available mineral nitrogen pool over the active leaching period. These results confirm that geologic nitrogen, when present, may be a large and reactive pool that may contribute as a non-point source of nitrate contamination to surface and ground waters. ?? 2001 Elsevier Science B.V. All rights reserved.
In situ quantification of Br and Cl in minerals and fluid inclusions by LA-ICP-MS: a powerful tool to identify fluid sources
Bromine and chlorine are important halogens for fluid source identification in the Earth's crust, but until recently we lacked routine analytical techniques to determine the concentration of these elements in situ on a micrometer scale in minerals and fluid inclusions. In this study, we evaluate the potential of in situ Cl and Br measurements by LA-ICP-MS through analysis of a range of scapolite grains with known Cl and Br concentrations. We assess the effects of varying spot sizes, variable plasma energy and resolve the contribution of polyatomic interferences on Br measurements. Using well-characterised natural scapolite standards, we show that LA-ICP-MS analysis allows measurement of Br and Cl concentrations in scapolite, and fluid inclusions as small as 16 μm in diameter and potentially in sodalite and a variety of other minerals, such as apatite, biotite, and amphibole. As a demonstration of the accuracy and potential of Cl and Br analyses by LA-ICP-MS, we analysed natural fluid inclusions hosted in sphalerite and compared them to crush and leach ion chromatography Cl/Br analyses. Limit of detection for Br is ~8 μg g −1 , whereas relatively high Cl concentrations (> 500 μg g −1 ) are required for quantification by LA-ICP-MS. In general, our LA-ICP-MS fluid inclusion results agree well with ion chromatography (IC) data. Additionally, combined cathodoluminescence and LA-ICP-MS analyses on natural scapolites within a well-studied regional metamorphic suite in South Australia demonstrate that Cl and Br can be quantified with a ~25 μm resolution in natural minerals. This technique can be applied to resolve a range of hydrothermal geology problems, including determining the origins of ore forming brines and ore deposition processes, mapping metamorphic and hydrothermal fluid provinces and pathways, and constraining the effects of fluid–rock reactions and fluid mixing.
Genesis of oil in metalliferous veins, San Juan Mountains, Colorado
A tarry, benzene-soluble material is present in metal-rich veins in the Idarado mine, Ouray, Colo., in an area not known to have petroleum resources. The material was compared chemically, spectrometrically, and chromatographically with oils from four fields in the nearby Paradox basin. Each oil field contains reservoir rocks equivalent to rock units known to extend beneath volcanic rocks near the mine. Carbon and sulfur isotope data and gas chromatographic data indicate a similarity between the oil from the Sierra field and the "oil" from the mine. Thus, the origin of the vein oil from Cretaceous sediments seems both geologically and chemically possible.