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At least 469 records · Page 26Linked to original sources
USGS1983

The past is the key to the future

A new major frontier of geological research, which was initiated in the 1970's, involves predicting future geologic trends or events through study of the present and past, rather than trying to understand the past, often using what one knows about the present. Like most scientific frontiers, this one began from practical considerations—environmental concerns. The lack of formal recognition of this frontier results from fragmentation among many Federal agencies and highly focused mission-oriented programs ( e.g. , earthquake prediction, CO 2 , nuclear-energy safety, etc.). Most programs aim to predict only the next 50–100 years, but much longer periods of the past need to be studied to do this. Nuclear-waste disposal has sometimes been considered in terms of the next million years, a period of time permitting significant and broad geologic changes. Decreasing public interest in environmental concerns relegates many questions from the realm of applied research back to that of basic research. Most of these questions are so fascinating, however, that the frontier is still worth pursuing. Such questions include whether a phenomenon will or will not take place and the rates at which it can develop ( e.g. , how fast do rifts form, how fast can a caldera event begin, and how quickly can a glacial maximum arrive?). Common elements of all studies include the historic record, trends in the Quaternary, analogues in various periods of the geologic time scale, and allowance for phenomena never experienced before. Other examples of studies include the Cretaceous as a period of a climatic extreme, an especially interesting time period; establishing the amount of paleocloudiness, a particularly challenging and important research area; acid rain as a possible new phenomenon. Geochemistry has much to contribute to this frontier science.

Geochimica et Cosmochimica Acta↗
USGS2015

Detailed description of oil shale organic and mineralogical heterogeneity via fourier transform infrared mircoscopy

Mineralogical and geochemical information on reservoir and source rocks is necessary to assess and produce from petroleum systems. The standard methods in the petroleum industry for obtaining these properties are bulk measurements on homogenized, generally crushed, and pulverized rock samples and can take from hours to days to perform. New methods using Fourier transform infrared (FTIR) spectroscopy have been developed to more rapidly obtain information on mineralogy and geochemistry. However, these methods are also typically performed on bulk, homogenized samples. We present a new approach to rock sample characterization incorporating multivariate analysis and FTIR microscopy to provide non-destructive, spatially resolved mineralogy and geochemistry on whole rock samples. We are able to predict bulk mineralogy and organic carbon content within the same margin of error as standard characterization techniques, including X-ray diffraction (XRD) and total organic carbon (TOC) analysis. Validation of the method was performed using two oil shale samples from the Green River Formation in the Piceance Basin with differing sedimentary structures. One sample represents laminated Green River oil shales, and the other is representative of oil shale breccia. The FTIR microscopy results on the oil shales agree with XRD and LECO TOC data from the homogenized samples but also give additional detail regarding sample heterogeneity by providing information on the distribution of mineral phases and organic content. While measurements for this study were performed on oil shales, the method could also be applied to other geological samples, such as other mudrocks, complex carbonates, and soils.

Energy & Fuels↗
USGS2014

Geochemical investigation of the hydrothermal system on Akutan Island, Alaska, July 2012

We have studied the geochemistry of the hot springs on Akutan Island in detail for the first time since the early 1980s. Springs in four discrete groups (A-D) along Hot Springs Creek showed generally higher temperatures and substantially higher Na, Ca, and Cl concentrations than previously reported, and total hot-spring discharge has also increased markedly. The springs now account for a heat output of ~29 MW, about an order of magnitude more than in 1981. Gas samples from the hot springs and from a fumarolic area on the flank of Akutan Volcano show high 3 He/ 4 He ratios (>6.4 RA) after correction for air contamination and reveal a common magmatic heat source. Hot-spring gases are unusually rich in N 2 , Ar, and CH 4 , suggesting that the water has boiled and lost CO 2 during upflow beneath the flank fumarole field. Gas geothermometry calculations applied to the flank fumarole field implies temperatures of 200–240 °C for the reservoir, and Na-K-Ca geothermometry implies temperatures near 180 °C for the outflow waters that feed the hot springs. The results of our study confirm the existence of a substantial geothermal resource on the island.

Alaska↗
USGS2005

Geochemistry and characteristics of nitrogen transport at a confined animal feeding operation in a coastal plain agricultural watershed, and implications for nutrient loading in the Neuse River basin, North Carolina, 1999-2002

Chemical, geologic, hydrologic, and age-dating information collected between 1999 and 2002 were used to examine the transport of contaminants, primarily nitrogen, in ground water and the pathways to surface water in a coastal plain setting in North Carolina. Data were collected from more than 35 wells and 4 surface-water sampling sites located in a 0.59 square-mile basin to examine detailed hydrogeology and geochemical processes affecting nutrient fate and transport. Two additional surface-water sampling sites were located downstream from the primary study site to evaluate basin-scale effects. Chemical and flow data also were collected at an additional 10 sites in the Coastal Plain portion of the Neuse River basin located between Kinston and New Bern, North Carolina, to evaluate loads transported in the Neuse River and primary tributary basins. At the Lizzie Research Station study site in North Carolina, horizontal flow is induced by the presence of a confining unit at shallow depth. Age-dating, chemical, and piezometric data indicate that horizontal flow from the surficial aquifer is the dominant source of ground water to streamflow. Nitrogen applied on cultivated fields at the Lizzie Research Station is substantially reduced as it moves from recharge to discharge areas. Denitrification in deeper parts of the aquifer and in riparian zones is indicated by a characterization of redox conditions in the aquifer and by the presence of excess nitrogen gas. Direct ground-water discharge of nitrate to surface water during base-flow conditions is unlikely to be significant because of strongly reducing conditions that occur in the riparian zones of these streams. Nitrate loads from a drainage tile at the study site may account for much of the nitrate load in the receiving stream, indicating that a major source of nutrients from ground water to this stream is artificial drainage. During base-flow conditions when the streams are not flowing, it is hypothesized that the mineralization of organic matter on the streambed is the source of nitrate and(or) ammonium in the stream. Base flow is a small contributor to nitrogen loads, because both flows and inorganic nitrogen concentrations are low during summer months. Effects of a confined hog operation on ground-water quality also were evaluated. The use of sprayed swine wastes to fertilize crops at the Lizzie Research Station study site since 1995 resulted in increased concentrations of nitrate and other chemical constituents in ground water beneath spray fields when compared to ground water beneath fields treated with commercial fertilizer. The nitrate concentration in ground water from the spray field well increased by a factor of 3.5 after 4 years of spray applications. Nitrate concentrations ranged from 10 to 35 milligrams per liter, and one concentration as high as 56 milligrams per liter was observed in water from this well in spring 2002. This finding is in agreement with findings of other studies conducted in the Coastal Plain of North Carolina that nitrate concentrations were significantly higher in ground water from cultivated fields sprayed with swine wastes than from fields treated with commercial fertilizer. Loads and yields of nitrogen and phosphorus in 14 streams in the Neuse River basin were evaluated for calendar years 2000 and 2001. Data indicate that anthropogenic effects on nitrogen yields were greatest in the first-order stream studied (yields were greater than 2 tons per square mile [ton/mi2] and 1 ton/mi2 or less in second- and higher-order streams) in the Little Contentnea Creek subbasin. Nitrogen yields in streams in the Contentnea Creek subbasin ranged from 0.59 to 2 ton/mi2 with typical yields of approximately 1 ton/mi2. Contentnea Creek near Evansdale had the highest yield (2 ton/mi2), indicating that a major source of nitrogen is upstream from this station. Nitrogen yields were lower at Contentnea Creek at Hookerton in 2000 and 2001 compared to previous yi

Scientific Investigations Report↗
USGS2025

A joint Gaussian process model of geochemistry, geophysics, and temperature for groundwater TDS in the San Ardo Oil Field, California, USA

Decline in availability of fresh groundwater has expanded interest in brackish groundwater resources; however, the distribution of brackish groundwater is poorly understood. Water resources in sedimentary basins across the United States often overlie oil and gas development. Mapping of groundwater total dissolved solids (TDS) using data from oil well geophysical logs has become an important technique for identifying fresh and brackish groundwater. Existing geophysical log analysis methods use porosity and temperature to relate formation resistivity to TDS. Typically, natural geothermal gradients are used to estimate temperature at the location of collected resistivity. However, in thermally enhanced oil fields, steam is injected into the subsurface to mobilize high viscosity oil, creating variable temperature distributions. Furthermore, TDS derived from resistivity also depends on the fractions of dominant ions. Typically, chloride and bicarbonate fractions must be determined. It is also necessary to model TDS across many geologic units with heterogenous porosity distributions. Collectively, each quantity used to estimate TDS (resistivity, porosity, temperature, bicarbonate fraction) varies in space and time, and available data points are rarely collocated. Here, we present a new method of mapping groundwater TDS that continuously models each quantity together with a joint Gaussian process. This method enables mapping fresh and brackish water with practically available data. We apply this method to the San Ardo Oil Field in Monterey County, California, where steam injection occurs. In some areas of the aquifer system overlying the oil zone, the temperature is ∼75 °C, roughly twice the natural background value. Groundwater TDS is typically <1,500 mg/L in the aquifer and increases with depth to ∼9,000 mg/L in the oil-producing zone. A low-permeability clay layer delineates the fresh and brackish water, likely by inhibiting surface recharge from penetrating the deeper zones, allowing higher-TDS connate water to remain in place. Weaker lateral TDS trends may be controlled by recharge patterns associated with the Salinas River. Our model reveals with high certainty that groundwater has freshened in one localized part of the oil-producing zone and suggests with less certainty that more widespread freshening has also occurred. The lowering of TDS was possibly from decades of low-TDS steam injection and the associated fluid production and disposal operations.

California↗
USGS2003

Petroleum system and production characteristics of the Muddy (J) Sandstone (Lower Cretaceous) Wattenberg continuous gas field, Denver basin, Colorado

Wattenberg field is a continuous-type gas accumulation. Estimated ultimate recovery from current wells is 1.27 tcf of gas from the Lower Cretaceous Muddy (J) Sandstone. Mean gas resources that have the potential to be added to these reserves in the next 30 yr are 1.09 tcf; this will be primarily through infill drilling to recover a greater percentage of gas in place and to drain areas that are isolated because of geologic compartmentalization. Greatest gas production from the Muddy (J) Sandstone in Wattenberg field occurs (1) from within the most permeable and thickest intervals of Fort Collins Member delta-front and nearshore-marine sandstones, (2) to a lesser extent from the Horsetooth Member valley-fill channel sandstones, (3) in association with a large thermal anomaly that is delineated by measured temperatures in wells and by vitrinite reflectance contours of 0.9% and greater, (4) in proximity to the bounding Mowry, Graneros, and Skull Creek shales that are the hydrocarbon source rocks and reservoir seals, and (5) between the Lafayette and Longmont right-lateral wrench fault zones (WFZs) with secondary faults that act as conduits in areas of the field. The axis of greatest gas production is north 25 to 35 degrees northeast, which parallels the basin axis. Recurrent movement along five right-lateral WFZs that crosscut Wattenberg field shifted the Denver basin axis to the northeast and influenced depositional and erosional patterns of the reservoir and seal intervals. Levels of thermal maturity within the Wattenberg field are anomalously high compared to other areas of the Denver basin. The Wattenberg field thermal anomaly may be due to upward movement of fluids along faults associated with probable igneous intrusions. Areas of anomalous high heat flow within the field correlate with an increased and variable gas-oil ratio. Debra Higley has 5 years experience in uranium exploration and 20 years as a petroleum geologist with the U.S. Geological Survey. Her research interests include and integrate reservoir characterization, thermal maturation studies, and petroleum resource assessment in basins in North and South America. She received a B.S. degree in geology from Mesa State College (Colorado) and an M.S. degree in geochemistry and Ph.D. in geology from the Colorado School of Mines.Dave Cox is vice president of Reservoir Engineering for Questa Engineering in Golden, Colorado. He has 25 years experience in the oil and gas industry, primarily in reservoir engineering and property evaluations, and has analyzed reservoirs in 31 states of the United States and 19 other countries. He is an expert in coalbed methane, tight gas reservoirs, and enhanced oil recovery. He has B.S. and M.S. degrees in petroleum engineering from the Colorado School of Mines. Robert Weimer has taught courses in stratigraphy, regional and field geology, and energy resource exploration and development for 43 years. He earned B.A. and M.A. degrees from the University of Wyoming and his Ph.D. from Stanford University. He has been a visiting professor at universities in Calgary, Canada; Adelaide, Australia; and Bandung, Indonesia. He is currently professor emeritus, Colorado School of Mines. Weimer has been honored for teaching excellence, blending basic and applied research, national and international continuing education, and service to scientific societies and to state and national boards.

Colorado↗
USGS2009

DayCent-Chem simulations of ecological and biogeochemical processes of eight mountain ecosystems in the United States

Atmospheric deposition of nitrogen (N) and sulfur (S) cause complex responses in ecosystems, from fertilization to forest ecosystem decline, freshwater eutrophication to acidification, loss of soil base cations, and alterations of disturbance regimes. DayCent-Chem, an ecosystem simulation model that combines ecosystem nutrient cycling and plant dynamics with aqueous geochemical equilibrium calculations, was developed to address ecosystem responses to combined atmospheric N and S deposition. It is unique among geochemically-based models in its dynamic biological cycling of N and its daily timestep for investigating ecosystem and surface water chemical response to episodic events. The model was applied to eight mountainous watersheds in the United States. The sites represent a gradient of N deposition across locales, from relatively pristine to N-saturated, and a variety of ecosystem types and climates. Overall, the model performed best in predicting stream chemistry for snowmelt-dominated sites. It was more difficult to predict daily stream chemistry for watersheds with deep soils, high amounts of atmospheric deposition, and a large degree of spatial heterogeneity. DayCent-Chem did well in representing plant and soil carbon and nitrogen pools and fluxes. Modeled stream nitrate (NO 3 - ) and ammonium (NH 4 + ) concentrations compared well with measurements at all sites, with few exceptions. Simulated daily stream sulfate (SO 4 2- ) concentrations compared well to measured values for sites where SO 4 2- deposition has been low and where SO 4 2- adsorption/desorption reactions did not seem to be important. The concentrations of base cations and silica in streams are highly dependent on the geochemistry and weathering rates of minerals in each catchment, yet these were rarely, if ever, known. Thus, DayCent-Chem could not accurately predict weathering products for some catchments. Additionally, few data were available for exchangeable soil cations or the magnitude of base cation deposition as a result of dry and fog inputs. The uncertainties related to weathering reactions, deposition, soil cation exchange capacity, and groundwater contributions influenced how well the simulated acid neutralizing capacity (ANC) and pH estimates compared to observed values. Daily discharge was well represented by the model for most sites. The chapters of this report describe the parameterization for each site and summarize model results for ecosystem variables, stream discharge, and stream chemistry. This intersite comparison exercise provided insight about important and possibly not well understood processes.

Scientific Investigations Report↗
USGS2021

Machine learning models of arsenic in private wells throughout the conterminous United States as a tool for exposure assessment in human health studies

Arsenic from geologic sources is widespread in groundwater within the United States (U.S.). In several areas, groundwater arsenic concentrations exceed the U.S. Environmental Protection Agency maximum contaminant level of 10 μg per liter (μg/L). However, this standard applies only to public-supply drinking water and not to private-supply, which is not federally regulated and is rarely monitored. As a result, arsenic exposure from private wells is a potentially substantial, but largely hidden, public health concern. Machine learning models using boosted regression trees (BRT) and random forest classification (RFC) techniques were developed to estimate probabilities and concentration ranges of arsenic in private wells throughout the conterminous U.S. Three BRT models were fit separately to estimate the probability of private well arsenic concentrations exceeding 1, 5, or 10 μg/L whereas the RFC model estimates the most probable category (≤5, >5 to ≤10, or >10 μg/L). Overall, the models perform best at identifying areas with low concentrations of arsenic in private wells. The BRT 10 μg/L model estimates for testing data have an overall accuracy of 91.2%, sensitivity of 33.9%, and specificity of 98.2%. Influential variables identified across all models included average annual precipitation and soil geochemistry. Models were developed in collaboration with public health experts to support U.S.-based studies focused on health effects from arsenic exposure.

Environmental Science and Technology↗
USGS1990

Geochemistry of batch-extract waters derived from spoil material collected at the Cordero coal mine, Powder River basin, Wyoming

Batch-mixing experiments to evaluate postmining water quality at the Cordero Mine were conducted by the U.S. Geological Survey during 1984 to 1985. Contact of groundwater from the spoil aquifer with fresh spoil material caused only small changes in major-element concentrations and in pH, unless sulfide oxidation or contact with soluble salts, such as epsomite, occurred. In contrast, large changes in major-element concentration resulted when water from the coal aquifer contacted the spoil material. Only three of seven reaction models considered to explain the water quality changes during the batch-mixing experiments were consistent with the thermodynamic and mineralogical data. The three models used to account for the observed water quality changes derived potassium from potassium feldspar; magnesium from chlorite or epsomite or both; sodium from cation exchange and halite; chloride from halite; silica from potassium feldspar and chlorite; sulfate from gypsum, or epsomite or both, and carbon from carbon dioxide. In general, water quality samples obtained from the batch-mixing experiments using water from the coal aquifer had smaller major-ion concentrations than the actual water quality in the spoil aquifer. These differences can be explained by the limited amount of efflorescent salt dissolution and volume of water used in the experiments. Correction ratios calculated for these experiments may be applied to batch-mixing experiments at other mines in the area, to predict postmining water quality. (USGS)

Water-Resources Investigations Report↗
USGS1992

Reconnaissance exploration geochemistry in the central Brooks Range, northern Alaska: Implications for exploration of sediment-hosted zinc-lead-silver deposits

A reconnaissance geochemical survey was conducted in the southern Killik River quadrangle, central Brooks Range, northern Alaska. The Brooks Range lies within the zone of continuous permafrost which may partially inhibit chemical weathering and oxidation. The minus 30-mesh and nonmagnetic heavy-mineral concentrate fractions of sediment samples were chosen as the sample media for the survey so that mechanical rather than chemical dispersion patterns would be enhanced. A total of 263 sites were sampled within the southern half of the Killik River quadrangle at an average sample density of approximately one sample per 12 km 2 . All samples were submitted for multi-element analyses. In the western and central Brooks Range, several known sediment-hosted Zn-Pb-Ag(-Ba) deposits occur within a belt of Paleozoic rocks of the Endicott Mountains allochthon. Exploration for this type of deposit in the Brook Range is difficult, due to the inherently high background values for Ba, Zn and Pb in shale and the common occurrence of metamorphic quartz-calcite veins, many of which contain traces of sulfide minerals. Stream sediments derived from these sources produce numerous geochemical anomalies which are not necessarily associated with significant mineralization. R-mode factor analysis provides a means of distinguishing between element associations related to lithology and those related to possible mineralization. Factor analysis applied to the multi-element data from the southern Killik River quadrangle resulted in the discovery of two additional Zn-Pb-Ag mineral occurrences of considerable areal extent which are 80–100 km east of any previously known deposit. These have been informally named the Kady and Vidlee. Several lithogeochemical element associations, or factors, and three factors which represent sulfide mineralization were identified: Ag-Pb-Zn (galena and sphalerite) and Fe-Ni-Co-Cu (pyrite ± chalcopyrite) in the concentrate samples and Cd-Zn-Pb-As-Mn in the sediment samples. The distribution of high scores for each individual mineralization factor outlined several relatively large (200–250 km 2 ) geochemically favorable areas. When the distribution of high scores for all three factors were superimposed, samples characterized by high scores for one or both of the concentrate mineralization factors and the mineralization factor in sediments define basin areas of approximately 48 and 64 km 2 surrounding Kady and Vidlee, respectively.

Journal of Geochemical Exploration↗
USGS2018

Geochemistry and mineralogy of late Quaternary loess in the upper Mississippi River valley, USA: Provenance and correlation with Laurentide Ice Sheet history

The midcontinent of North America contains some of the thickest and most extensive last-glacial loess deposits in the world, known as Peoria Loess. Peoria Loess of the upper Mississippi River valley region is thought to have had temporally varying glaciogenic sources resulting from inputs of sediment to the Mississippi River from different lobes of the Laurentide Ice Sheet. Here, we explore a new method of determining loess provenance using K/Rb and K/Ba values (in K-feldspars and micas) in loess from a number of different regions in North America. Results indicate that K/Rb and K/Ba values can distinguish loess originating from diverse geologic terrains in North America. Further, different loess bodies that are known to have had the same source sediments (using other criteria) have similar K/Rb and K/Ba values. We also studied three thick loess sections in the upper Mississippi River valley region. At each site, the primary composition of the loess changed over the course of the last glacial period, and K/Rb and K/Ba values parallel changes in carbonate mineral content and clay mineralogy. We thus confirm conclusions of earlier investigators that loess composition changed as a result of the shifting dominance of different lobes of the Laurentide Ice Sheet and the changing course of the Mississippi River. We conclude that K/Rb and K/Ba values are effective, robust, and rapid indicators of loess provenance that can be applied to many regions of the world.

Quaternary Science Reviews↗
USGS2022

Multidisciplinary constraints on the thermal-chemical boundary between Earth's core and mantle

Heat flux from the core to the mantle provides driving energy for mantle convection thus powering plate tectonics, and contributes a significant fraction of the geothermal heat budget. Indirect estimates of core-mantle boundary heat flow are typically based on petrological evidence of mantle temperature, interpretations of temperatures indicated by seismic travel times, experimental measurements of mineral melting points, physical mantle convection models, or physical core convection models. However, previous estimates have not consistently integrated these lines of evidence. In this work, an interdisciplinary analysis is applied to co-constrain core-mantle boundary heat flow and test the thermal boundary layer (TBL) theory. The concurrence of TBL models, energy balance to support geomagnetism, seismology, and review of petrologic evidence for historic mantle temperatures supports Q CMB ∼15 TW, with all except geomagnetism supporting as high as ∼20 TW. These values provide a tighter constraint on core heat flux relative to previous work. Our work describes the seismic properties consistent with a TBL, and supports a long-lived basal mantle molten layer through much of Earth's history.

Geochemistry, Geophysics, Geosystems↗
USGS2020

Distribution of earthquakes on a branching fault system using integer programming and greedy sequential methods

A new global optimization method is used to determine the distribution of earthquakes on a complex, connected fault system. The method, integer programming, has been advanced in the field of operations research, but has not been widely applied to geophysical problems until recently. In this application, we determine the optimal distribution of earthquakes on mapped faults to minimize the global misfit in slip rates for multi-fault ruptures. Integer programming solves for a decision vector composed of every possible location that a sample of earthquakes can occur on every fault, subject to slip-rate uncertainty constraints. Step over connections are straightforward to include, whereas branching fault connections are not. To include branching ruptures, we distinguish between individual multi-fault rupture paths, as opposed to formulating the integer-programming problem based on individual faults as in previous studies. The new method is applied to the complex fault system in the San Francisco Bay Area as a case study. Results from the integer-programming method are compared to those from a local optimization method, termed the greedy-sequential method. Several experiments using these two methods indicate that shape of the on-fault magnitude distributions and which branching faults are involved in multi-fault ruptures depend on how much emphasis is placed on fitting the target slip rate. In cases where the underlying data are not strong enough to warrant chasing the target slip rate, it is better to focus on the distribution of feasible results that better represents the uncertainty in the solutions imposed by the data.

Geochemistry, Geophysics, Geosystems↗
USGS2011

Quality assurance and quality control of geochemical data&mdash;A primer for the research scientist

Geochemistry is a constantly expanding science. More and more, scientists are employing geochemical tools to help answer questions about the Earth and earth system processes. Scientists may assume that the responsibility of examining and assessing the quality of the geochemical data they generate is not theirs but rather that of the analytical laboratories to which their samples have been submitted. This assumption may be partially based on knowledge about internal and external quality assurance and quality control (QA/QC) programs in which analytical laboratories typically participate. Or there may be a perceived lack of time or resources to adequately examine data quality. Regardless of the reason, the lack of QA/QC protocols can lead to the generation and publication of erroneous data. Because the interpretations drawn from the data are primary products to U.S. Geological Survey (USGS) stakeholders, the consequences of publishing erroneous results can be significant. The principal investigator of a scientific study ultimately is responsible for the quality and interpretation of the project's findings, and thus must also play a role in the understanding, implementation, and presentation of QA/QC information about the data. Although occasionally ignored, QA/QC protocols apply not only to procedures in the laboratory but also in the initial planning of a research study and throughout the life of the project. Many of the tenets of developing a sound QA/QC program or protocols also parallel the core concepts of developing a good study: What is the main objective of the study? Will the methods selected provide data of enough resolution to answer the hypothesis? How should samples be collected? Are there known or unknown artifacts or contamination sources in the sampling and analysis methods? Assessing data quality requires communication between the scientists responsible for designing the study and those collecting samples, analyzing samples, treating data, and interpreting results. This primer has been developed to provide basic information and guidance about developing QA/QC protocols for geochemical studies. It is not intended to be a comprehensive guide but rather an introduction to key concepts tied to a list of relevant references for further reading. The guidelines are presented in stepwise order beginning with presampling considerations and continuing through final data interpretation. The goal of this primer is to outline basic QA/QC practices that scientists can use before, during, and after chemical analysis to ensure the validity of the data they collect with the goal of providing defendable results and conclusions.

Open-File Report↗
USGS1974

Red Sea geochemistry

The Red Sea drillings reveal a number of new facets of the hot-brine-metalliferous system and other geochemical aspects of the sea, its sediments, and its past history as follows: 1) Dark shales rich in organic material, and containing enhanced Mo and V concentrations, are characteristic of Plio-Pleistocene strata in the Red Sea. Values as high as 1500 ppm V and 500 ppm Mo were obtained in sediments containing up to 8 percent organic carbon. 2) Metalliferous sediments in the hot brine deep (Site 226) are similar in composition in both solids and interstitial water to previously analyzed sediments. However, one site (228) well south of the known hot-brine deeps shows zinc mineralization reaching 5 percent Zn in late Miocene shale-anhydrite breccias. 3) Pore fluid studies show that near-saturated (NaCl) brines having similar total salt concentration to the hot-brine fluids are associated with Miocene evaporites at Sites 225, 227, and 228. However, their chemical and isotopic composition precludes such fluids being part of the "hot brine plumbing system." Hydrogen and oxygen isotope studies demonstrate that fluids trapped between and among the evaporitic rocks have a strong meteoric water component, presumed to have entered the rocks during or shortly after formation in shallow evaporating pans. The composition of pore fluid at Site 227 suggests the presence of late-stage evaporite minerals of the tachyhydrite CaMg 2 Cl 6 • 12H 2 O series in the in situ rocks. 4) Diffusivity measurements show that the pre-Miocene strata permit dissolved salt or gas diffusion to the extent of from 1/2 to about 1/10 the rate in free solution. However, in anhydrites diffusivity is reduced more than 100-fold, and no diffusion could be detected through halite rock. The rates applied to interstitial salt gradients at Site 225 suggest that less than 1 meter of rock salt is removed per million years by diffusion processes. The diffusion of salt can already be detected a few meters below the sediment-water interface, and based on the interstitial water studies, one can affirm the presence of salt at depth at Sites 228, 230, and possibly 229, where rock salt was not encountered by the drill. 5) Isotopic measurements on leads show that both leads from Site 228 and the hot brine deep (Site 226) require input from igneous or volcanic sources (e.g., volcanic ash). Elsewhere, however, leads of sedimentary-pelagic origin are noted. 6) Isotopic and other evidence indicates that the long-distance transport of subterranean brines advocated by Craig (1969) is unlikely. Instead, it is proposed that the source of the hot brines is subevaporite clastic or other aquifers of early to middle Miocene age that have been disrupted by rifting. These discharge in the deeps by virtue of hydrodynamic continuity with heavy brines at higher positions on the nearby flanks of the Red Sea. In this case, the waters might be fossil (middle Miocene) Red Sea waters of relatively normal salinity that have acquired greater salt concentration by diffusion from overlying late Miocene evaporites. The model is consistent with the isolated nature of the brine deeps and suggests that flow might have been enhanced by increased hydraulic gradients during periods of lowered Red Sea levels. 7) Interstitial water evidence indicates that Pleistocene lowerings of sea level did not cause evaporative conditions leading to actual gypsum or other evaporite deposition in the deeper water zones, as has been postulated. This in turn suggests that sill depths were greater than have been assumed.

Initial reports of the Deep Sea Drilling Project↗
USGS2009

Sediment-hosted zinc-lead deposits of the world— Database and grade and tonnage models

This report provides information on sediment-hosted zinc-lead mineral deposits based on the geologic settings that are observed on regional geologic maps. The foundation of mineral-deposit models is information about known deposits. The purpose of this publication is to make this kind of information available in digital form for sediment-hosted zinc-lead deposits. Mineral-deposit models are important in exploration planning and quantitative resource assessments: Grades and tonnages among deposit types are significantly different, and many types occur in different geologic settings that can be identified from geologic maps. Mineral-deposit models are the keystone in combining the diverse geoscience information on geology, mineral occurrences, geophysics, and geochemistry used in resource assessments and mineral exploration. Too few thoroughly explored mineral deposits are available in most local areas for reliable identification of the important geoscience variables, or for robust estimation of undiscovered deposits - thus, we need mineral-deposit models. Globally based deposit models allow recognition of important features because the global models demonstrate how common different features are. Well-designed and -constructed deposit models allow geologists to know from observed geologic environments the possible mineral-deposit types that might exist, and allow economists to determine the possible economic viability of these resources in the region. Thus, mineral-deposit models play the central role in transforming geoscience information to a form useful to policy makers. This publication contains a computer file of information on sediment-hosted zinc-lead deposits from around the world. It also presents new grade and tonnage models for nine types of these deposits and a file allowing locations of all deposits to be plotted in Google Earth. The data are presented in FileMaker Pro, Excel and text files to make the information available to as many as possible. The value of this information and any derived analyses depends critically on the consistent manner of data gathering. For this reason, we first discuss the rules applied in this compilation. Next, the fields of the data file are considered. Finally, we provide new grade and tonnage models that are, for the most part, based on a classification of deposits using observable geologic units from regional-scaled maps.

Open-File Report↗
USGS1994

Ground-water quality and geochemistry in Carson and Eagle Valleys, western Nevada and eastern California

Aquifers in Carson and Eagle Valleys are an important source of water for human consumption and agriculture. Concentrations of major constituents in water from the principal aquifers on the west sides of Carson and Eagle Valleys appear to be a result of natural geochemical reactions with minerals derived primarily from plutonic rocks. In general, water from principal aquifers is acceptable for drinking when compared with current (1993) Nevada State drinking-water maximum contaminant level standards. Water was collected and analyzed for all inorganic constituents for which primary or secondary drinking-water standards have been established. About 3 percent of these sites had con- stituents that exceeded one or more primary or secondary drinking-water standards have been established. About 3 percent of these sites had con- stituents that exceeded one or more primary standards and water at about 10 percent of the sites had at least one constituent that surpassed a secondary standard. Arsenic exceeded the standard in water at less than 1 percent of the principal aquifer sites; nitrate surpassed its standard in water at 3 percent of 93 sites. Water from wells in the principal aquifer with high concentrations of nitrate was in areas where septic systems are used; these concentrations indicate that contamination may be entering the wells. Concentrations of naturally occurring radionuclides in water from the principal aquifers, exceed the proposed Federal standards for some constituents, but were not found t be above current (1993) State standards. The uranium concen- trations exceeded the proposed 20 micrograms per liter Federal standard at 10 percent of the sites. Of the sites analyzed for all of the inorganic constituents with primary standards plus uranium, 15 percent exceed one or more established standards. If the proposed 20 micrograms per liter standard for uranium is applied to the sampled sites, then 23 percent would exceed the standard for uranium or some other constituent with a primary drinking water standard. This represents a 50-percent increase in the frequency of exceedance. Almost all water sampled from the principal aquifers exceeds the 300 picocuries per liter proposed standard for radon. Ground-water sampling sites with the highest radon activities in water are most commonly located in the upland aquifers in the Sierra Nevada and in the principal aquifers beneath the west sides of Carson and Eagle Valleys.

Open-File Report↗
USGS2019

Geographic attribution of soils using probabilistic modeling of GIS data for forensic search efforts

Examinations of soil traces associated with forensic evidence can be used to narrow potential source area(s) by characterizing features of the trace soil assemblage, some of which are limited to specific regions. Soil characteristics may be used to infer the likelihoods of the soil trace being derived from distinct areas within digital maps, including both maps of discrete classes such as formations on geologic maps and land cover, and continuous geospatial data, such as distance from a point source. Seldom do digital maps precisely represent the observable characteristics in a soil trace. Nevertheless, logical assigned likelihoods based on the correspondence between the mapped characteristics and the observed soil particulate assemblage permit creation of a model of the more probable sources of the soil trace. This approach is applied to a 2003 case in which forensic soil samples derived from digging tools were characterized for investigative leads and to narrow the search area of a clandestine grave. This grave site was located in 2005. The suspect traveled approximately 5,000 km before arrest, so narrowing the prioritized search area for law enforcement would be beneficial. Soil examination and case circumstances were used to assign relative likelihoods within digital maps (GIS or Geographic Information Systems data) of geology, soil mineralogy, plant distributions, power plant locations, and proximity to the known travel path. The product of these individual probability maps generates joint probability models to narrow the recommended search area. The digital model output can be easily overlaid on infrastructure maps to aid law enforcement searches.

Geochemistry, Geophysics, Geosystems↗