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USGS2002

Herbicide transport in rivers: Importance of hydrology and geochemistry in nonpoint-source contamination

Alachlor, atrazine, cyanazine, metolachlor, and metribuzin were measured at six sites during 1984 and 1985 in large subbasins within the Cedar River, IA. A computer model separated the Cedar River discharge hydrograph into groundwater and overland-flow components. The concentration of herbicides in the river when groundwater was the major flow component was less than 1.0 μ g/L and averaged 0.2 μ g/L. The maximum concentrations of herbicides occurred when overland flow was the major component of river discharge, exceeding 50 pg/L for total herbicides. About 6% of the annual river load of atrazine was transported with the groundwater component, while 94% was transported with overland flow. From 1.5 to 5% of the atrazine applied during the year was transported from the basin. Atrazine concentrations in the river in- creased according to the discharge divided by the drainage area. This correlation indicates that rivers with large normalized 2-year peak flows have the potential to transport large concentrations of herbicides. A diagrammatic model of nonpoint-source transport of herbicides was developed that suggests that sorbed transport from fields occurs during episodes of overland flow with rapid dissolution of herbicides downstream.

Iowa↗

USGS1985

Characterization of the Sukinda and Nausahi ultramafic complexes, Orissa, India by platinum-group element geochemistry

Samples of 20 chromitite, 14 ultramafic and mafic rock, and 9 laterite and soil samples from the Precambrian Sukinda and Nausahi ultramafic complexes, Orissa, India were analyzed for platinum-group elements (PGE). The maximum concentrations are: palladium, 13 parts per billion (ppb); platinum, 120 ppb; rhodium, 21 ppb; iridium, 210 ppb; and ruthenium, 630 ppb. Comparison of chondrite-normalized ratios of PGE for the chromitite samples of lower Proterozoic to Archean age with similar data from Paleozoic and Mesozoic ophiolite complexes strongly implies that these complexes represent Precambrian analogs of ophiolite complexes. This finding is consistent with the geology and petrology of the Indian complexes and suggests that plate-tectonic and ocean basin development models probably apply to some parts of Precambrian shield areas.

Precambrian Research↗

USGS2009

Radionuclides as tracers and timers in surface and groundwater

Environmental radionuclides—in combination with stable isotopes, geochemistry, and other hydrological techniques—provide a powerful tool, often indispensable, for studying the cycling of water in continental hydrological systems. The use of environmental radionuclides in surface water studies is reviewed in the chapter. The chapter also briefly discusses groundwater and geothermal water taking into consideration the fact that most applications in groundwater and geothermal water studies require the combined use of radioactive and stable isotopes. There are several sources of radionuclides in the environment, and the sources control the ways in which isotopes can be applied to hydrologic systems. Another group of radionuclides that can be utilized are those produced by cosmic-ray spallationin the atmosphere or near-surface lithosphere. Many of these nuclides, such as carbon-14 ( 14 C) and tritium ( 3 H), are also produced by nuclear weapons testing, and it is necessary to separate the two source functions when using them.

Book chapter↗

USGS2012

Groundwater quality in the Columbia Plateau, Snake River Plain, and Oahu basaltic-rock and basin-fill aquifers in the Northwestern United States and Hawaii, 1992-2010

This assessment of groundwater-quality conditions of the Columbia Plateau, Snake River Plain, and Oahu for the period 1992–2010 is part of the U.S. Geological Survey’s National Water Quality Assessment (NAWQA) program. It shows where, when, why, and how specific water-quality conditions occur in groundwater of the three study areas and yields science-based implications for assessing and managing the quality of these water resources. The primary aquifers in the Columbia Plateau, Snake River Plain, and Oahu are mostly composed of fractured basalt, which makes their hydrology and geochemistry similar. In spite of the hydrogeologic similarities, there are climatic differences that affect the agricultural practices overlying the aquifers, which in turn affect the groundwater quality. Understanding groundwater-quality conditions and the natural and human factors that control groundwater quality is important because of the implications to human health, the sustainability of rural agricultural economies, and the substantial costs associated with land and water management, conservation, and regulation. The principal regional aquifers of the Columbia Plateau, Snake River Plain, and Oahu are highly vulnerable to contamination by chemicals applied at the land surface; essentially, they are as vulnerable as many shallow surficial aquifers elsewhere. The permeable and largely unconfined character of principal aquifers in the Columbia Plateau, Snake River Plain, and Oahu allow water and chemicals to infiltrate to the water table despite depths to water commonly in the hundreds of feet. The aquifers are essentially unconfined over large areas, having few extensive clay layers to impede infiltration through permeable volcanic rock and alluvial sediments. Agriculture is intensive in all three study areas, and heavy irrigation has imposed large artificial flows of irrigation recharge that rival or exceed natural recharge rates. Fertilizers and pesticides applied at land surface are leached from soil and transported to deep water tables with the infiltrating irrigation recharge, resulting in a layer of degraded water quality overlying better quality regional groundwater beneath. This “irrigation-recharge layer” is best known on Oahu, where it has been studied since the 1960s; however, the extent of nitrate and pesticide contamination in the Columbia Plateau and Snake River Plain indicate that the same situation exists in those areas. Contamination from agricultural and urban activities is present not only at shallow depths in surficial materials of the three areas, but extends regionally in the deep, principal bedrock aquifers that are tapped for drinking water by domestic and public-supply wells. Naturally occurring constituents and nitrate concentrations above human-health benchmarks—Maximum Contaminant Levels (MCLs), and Health-Based Screening Levels (HBSLs)—were more common in the Columbia Plateau and the Snake River Plain than in Oahu. Concentrations of anthropogenic constituents (constituents related to human activities) above human-health benchmarks were more common in Oahu. Naturally occurring contaminants, such as arsenic and radon, may be present in groundwater at concentrations of potential concern for human health in relatively undeveloped settings that otherwise may not be perceived as susceptible to contamination. Even though the median depth to groundwater in Oahu is more than 300 feet, the common occurrence of anthropogenic compounds in groundwater indicates that Oahu has a high susceptibility to contamination. Nitrate concentrations in groundwater were above the national background concentrations of 1 milligram per liter (mg/L) in all three study areas. In the Columbia Plateau, nitrate exceeded the human-health benchmark of 10 mg/L in 20 percent of the wells sampled. In the Snake River Plain, nitrate exceeded the human-health benchmark of 10 mg/L in 3 percent of the wells sampled. Nitrate can persist in groundwater for years and even decades in the oxygen-rich groundwater of the Columbia Plateau and the Snake River Plain, so prudent groundwater protection measures are critical to protect drinking water resources by reducing nitrate leaching from the land surface. Nitrate logistic regression models indicated that areas with a high percentage of land in crops (such as potatoes or sugarcane) and soils with low amounts of organic matter are most likely to have elevated nitrate concentrations in the groundwater. Areas where agricultural activities were absent had much lower probabilities of detecting elevated nitrate concentrations. The Columbia Plateau had a much higher probability of having elevated nitrate concentrations, with most of the land area having greater than a 50 percent probability of elevated nitrate concentrations. Oahu and the Snake River Plain had a much lower probability of having elevated nitrate concentrations because of their lower percentage of agricultural land. Pesticides were detected at many sites in groundwater of the Columbia Plateau, Snake River Plain, and Oahu but generally at low concentrations below human-health benchmarks. Atrazine and its degradate (a compound produced from the breakdown of a parent pesticide), deethylatrazine, were the most commonly detected pesticides in groundwater sampled in the Columbia Plateau and Snake River Plain. Bromacil was the most commonly detected pesticide on Oahu. The other pesticides most commonly detected in the study areas include simazine, hexazinone, metribuzin, diuron, prometon, metolachlor, p,p’ -DDE, dieldrin, 2-4-D, and alachlor. DDE (a degradate of DDT) and dieldrin are still being detected in groundwater despite having been banned for more than 30 years. Codetection of multiple pesticides in water from a single well was common. The widespread occurrence of pesticides in groundwater in the study areas indicates that the groundwater is highly susceptible to pesticide contamination. Some pesticides were detected in groundwater samples from all three study areas, but other pesticides were detected only in samples from Oahu, or only in samples from the Columbia Plateau and Snake River Plain. This is because some pesticides (such as atrazine) are broad-spectrum pesticides that are used on many crops in many different areas of the United States. Other pesticides (such as simazine, metribuzin, and metolachlor) are used on row crops (such as potatoes, barley, and alfalfa) grown in the Columbia Plateau and Snake River Plain, but not on pineapple or sugarcane grown in Oahu. Atrazine logistic-regression models indicate that areas with a high percentage of land in crops (such as potatoes or sugarcane), a low percentage of fallow land, and highly permeable soils with low amounts of organic matter are most likely to have atrazine detected in the groundwater. Areas where agricultural activities were absent had much lower probabilities of atrazine being detected. The Snake River Plain had a much higher probability of atrazine detections, with more than 50 percent of the land area having greater than a 50 percent probability of atrazine contamination. Oahu had a much lower probability of atrazine contamination, with only 24 percent of the land area having greater than a 50 percent probability of atrazine contamination. Oahu and the Columbia Plateau had some of the highest percentages of soil fumigant detections in groundwater in the United States. Soil fumigants are volatile organic compounds (VOCs) used as pesticides, which are applied to soils to reduce populations of plant parasitic nematodes (harmful rootworms), weeds, fungal pathogens, and other soil-borne microorganisms. They are used in Oahu and the Columbia Plateau on crops such as pineapple and potatoes. All three areas (Columbia Plateau, Snake River Plain, and Oahu) had fumigant concentrations exceeding human-health benchmarks for drinking water.

Hawai'i, Idaho, Nevada, Oregon, Utah, Washington, ↗

USGS1990

Multivariate statistical analysis of stream-sediment geochemistry in the Grazer Paläozoikum, Austria

The Austrian reconnaissance study of stream-sediment composition — more than 30000 clay-fraction samples collected over an area of 40000 km 2 — is summarized in an atlas of regional maps that show the distributions of 35 elements. These maps, rich in information, reveal complicated patterns of element abundance that are difficult to compare on more than a small number of maps at one time. In such a study, multivariate procedures such as simultaneous R-Q mode components analysis may be helpful. They can compress a large number of variables into a much smaller number of independent linear combinations. These composite variables may be mapped and relationships sought between them and geological properties. As an example, R-Q mode components analysis is applied here to the Grazer Paläozoikum, a tectonic unit northeast of the city of Graz, which is composed of diverse lithologies and contains many mineral deposits.

Mineralium Deposita↗

USGS2000

Geochemical investigations by the U.S. Geological Survey on uranium mining, milling, and environmental restoration

Recent research by the U.S. Geological Survey has characterized contaminant sources and identified important geochemical processes that influence transport of radionuclides from uranium mining and milling wastes. 1) Selective extraction studies indicated that alkaline earth sulfates and hydrous ferric oxides are important hosts of 226 Ra in uranium mill tailings. The action of sulfate-reducing and ironreducing bacteria on these phases was shown to enhance release of radium, and this adverse result may temper decisions to dispose of uranium mill tailings in anaerobic environments. 2) Field studies have shown that although surface-applied sewage sludge/wood chip amendments aid in revegetating pyritic spoil, the nitrogen in sludge leachate can enhance pyrite oxidation, acidification of groundwater, and the consequent mobilization of metals and radionuclides. 3) In a U.S. Environmental Protection Agencyfunded study, three permeable reactive barriers consisting of phosphate-rich material, zero-valent iron, or amorphous ferric oxyhydroxide have been installed at an abandoned uranium upgrader facility near Fry Canyon, UT. Preliminary results indicate that each of the permeable reactive barriers is removing the majority of the uranium from the groundwater. 4) Studies on the geochemistry of rare earth elements as analogues for actinides such as uranium and thorium in acid mine drainage environments indicate high mobility under acid-weathering conditions but measurable attenuation associated with iron and aluminum colloid formation. Mass balances from field and laboratory studies are being used to quantify the amount of attenuation. 5) A field study in Colorado demonstrated the use of 234 U/ 238 U isotopic ratio measurements to evaluate contamination of shallow groundwater with uranium mill effluent.

Utah↗

USGS2016

Arsenic and radionuclide occurrence and relation to geochemistry in groundwater of the Gulf Coast Aquifer System in Houston, Texas, 2007–11

The U.S. Geological Survey (USGS), in cooperation with the City of Houston, began a study in 2007 to determine concentrations, spatial extent, and associated geochemical conditions that might be conducive for mobility and transport of selected naturally occurring trace elements and radionuclides in the Gulf Coast aquifer system in Houston, Texas. Water samples were collected from 91 municipal supply wells completed in the Evangeline and Chicot aquifers of the Gulf Coast aquifer system in northeastern, northwestern, and southwestern Houston; hereinafter referred to as northeast, northwest and southwest Houston areas. Wells were sampled in three phases: (1) 28 municipal supply wells were sampled during 2007–8, (2) 60 municipal supply wells during 2010, and (3) 3 municipal supply wells during December 2011. During each phase of sampling, samples were analyzed for major ions, selected trace elements, and radionuclides. At a subset of wells, concentrations of arsenic species and other radionuclides (carbon-14, radium-226, radium-228, radon-222, and tritium) also were analyzed. Selected physicochemical properties were measured in the field at the time each sample was collected, and oxidation-reduction potential and unfiltered sulfides also were measured at selected wells. The source-water (the raw, ambient water withdrawn from municipal supply wells prior to water treatment) samples were collected for assessment of aquifer conditions in order to provide community water-system operators information that could be important when they make decisions about which treatment processes to apply before distributing finished drinking water. Geochemical conditions of groundwater of the Gulf Coast aquifer system are suitable in some instances for release of arsenic and radionuclides from aquifer materials. Recent changes to the U.S. Environmental Protection Agency (EPA) primary drinking-water regulations for arsenic and a selected number of natural radionuclides have highlighted the necessity for municipal supply system managers to be aware of the occurrence and distribution of these constituents in their source water. Concentrations of arsenic ranged from 0.58 to 23.5 micrograms per liter (μg/L), with relatively low median and 75th percentile concentrations (2.7 and 3.6 μg/L, respectively). The gross alpha-particle activity completed within 72 hours after sample collection ranged from R-1.1 (nondetect where the result was below the sample specific critical level) to 39.7 picocuries per liter (pCi/L), with a median of 10.3 pCi/L. After 30 days, the gross alpha-particle activities in the 91 samples ranged from R-0.94 to 25.5 pCi/L, with a median of 5.60 pCi/L. Concentrations of uranium ranged from less than 0.02 to 42.7 μg/L, with a median value of 1.69 μg/L and a 75th-percentile value of 6.48 μg/L. The maximum concentrations of radium-226 and combined radium (sum of radium-226 plus radium-228) were 4.34 pCi/L and 3.23 pCi/L, respectively. Aquifer major-ion geochemistry was characterized and shown to contain three chemical types of water as grouped by a simplified predominant cation and anion classification system: (1) calcium- bicarbonate type, (2) sodium-bicarbonate type, and (3) sodium-chloride type. Aquifer geochemistry also was characterized into four reduction-oxidation (redox) categories: (1) oxic, (2) suboxic, (3) mixed, and (4) anoxic. Within the anoxic category, groundwater was further characterized into four presumed predominant reduction processes: (1) iron or sulfate or both [Fe(III)/SO 4 ] reducing, (2) iron [Fe(III)] reducing, (3) iron and sulfate [Fe(III)-SO 4 ] reducing, or (4) methanogenic, as defined by composition of redox species. The oxic category was associated with calcium-bicarbonate-type water, and the methanogenic-anoxic process was associated exclusively with the sodium-bicarbonate-type water. The species of arsenic and the dominant radionuclide present were associated with specific redox categories. Arsenate was associated primarily with oxic water and did not exceed 3.5 µg/L, whereas arsenite was associated with iron-reducing, anoxic water samples and, at the highest concentrations, occurred in sulfate-reducing, anoxic; methanogenic-anoxic; or both water samples. Uranium was associated exclusively with the oxic water, whereas the highest concentrations of combined radium were associated with the iron-reducing, anoxic water. The gross alpha-particle activity was greatest in the oxic waters where the source of the radioactivity was the uranium. Associated geochemical conditions conducive for mobility of arsenic and radionuclides and their spatial and vertical extent in the Gulf Coast aquifer system in Houston are important aspects to the areal management of the municipal groundwater supplies in Houston. Ongoing research is seeking to define chemical or geological factors that are the optimal indicators for elevated concentrations of these naturally occurring constituents.

Texas↗

USGS1987

The geochemistry of water near a surficial organic-rich uranium deposit, northeastern Washington State, U.S.A.

The chemistry of three stream, three spring and six near-surface waters in the vicinity of a Holocene organic-rich uranium deposit is described, with particular emphasis on the chemistry of U. Results characterize the solution behavior of uranium as U-bearing water interacts with relatively undecomposed, surficial organic matter. Of the measured major and trace chemical species, only U is consistently highly enriched (17-318 ppb) relative to reported values for regional waters, or to literature values for waters in largely granitic terrains. R-mode factor analysis of the chemical data suggests that most U is present in a soluble form, but that some U is also associated with fine suspended particulates of clay, organic matter, or hydrous oxides. Calculations that apply thermodynamic data to predict U speciation in solution indicate the relative importance of uranyl carbonate and uranyl phosphate complexes. Analysis of more finely filtered samples (0.05 ??m vs. 0.45 ??m), and direct radiographic observations using fission-track detectors suspended in the waters indicate the presence of some uraniferous particulate matter. Application of existing thermodynamic data for uranous- and uranyl-bearing minerals indicates that all waters are undersaturated with U minerals as long as ambient Eh ??? +0.1 v. If coexisting surface and near-surface waters are sufficiently oxidizing, initial fixation of U in the deposit should be by a mechanism of adsorption. Alternatively, more reducing conditions may prevail in deeper pore waters of the organic-rich host sediments, perhaps leading to direct precipitation or diagenetic formation of U4+ minerals. A 234U 238U alpha activity ratio of 1.08 ?? 0.02 in a spring issuing from a hillslope above the deposit suggests a relatively soluble source of U. In contrast, higher activity ratios of 234U 238U (??? 1.3) in waters in contact with the uraniferous valley-fill sediments suggest differences in the nature of interaction between groundwater and the local, U-rich source rocks. ?? 1987.

Chemical Geology↗

USGS1997

Geologic studies in Alaska by the U.S. Geological Survey, 1995

This collection of 20 papers continues the annual series of U.S. Geological Survey (USGS) reports on geologic investigations in Alaska1 . Contributions cover a broad spectrum of earth science topics and report results from all parts of the State (fig. 1). USGS activities in Alaska include studies of environment and climate, hazards, resources, and geologic framework. Five papers in this volume discuss aspects of environment and climate. Environmental geochemistry of parts of southwestern and south-central Alaska is the focus of four articles; a fifth study, of emergent postglacial lake shorelines in southwestern Alaska, contributes to ongoing investigations of paleoclimate. Two papers address geologic hazards. The first assesses ground deformation in Katmai National Park at Novarupta dome, site of the largest volcanic eruption in this century, and the second evaluates earthquake risks related to the "Twin Peak fault" near Anchorage. Resources, including metallic minerals in northern, southwestern, and southeastern Alaska and coal in south-central Alaska, are discussed in four articles. Nine geologic framework studies apply a variety of techniques to a wide range of subjects throughout Alaska, including tectonics, geophysics, geochronology, bio stratigraphy, sedimentology, paleogeography, and paleomagnetism. Two bibliographies at the end of the volume list reports about Alaska in USGS publications released in 1995 and reports about Alaska by USGS authors in non-USGS publications in 1995.

Alaska↗

USGS2019

The Orange Tuff: A Late Pleistocene tephra-fall deposit emplaced by a VEI 5 silicic Plinian eruption in West Java, Indonesia

A VEI 5 dacite eruption emplaced the Orange Tuff about between 34.3 cal kBP and 17.2 cal kBP. Gunung Salak is the unit’s source and the Orange Tuff represents the most recent such eruption from any of the volcanoes southwest of Bogor, Indonesia. The Orange Tuff is the region’s first such documented tephra-fall deposit whose characteristics and phenocryst geochemistry make it readily identifiable over at least 1250 km 2 . Magnetite compositions and temperature and f O 2 estimates inferred from Fe-Ti oxide compositions are particularly useful for identifying the unit. Deposit characteristics suggest that the eruption lasted 1–11 h with mass eruption rates of 1.0–8.3 × 10 8 kg/s and a column height of 31–40 km. The eruption’s column height and the deposit’s 2.5–11 km 3 volume suggest that the unit was dispersed over a much wider area than mapped. The unit is a marker bed throughout its mapped distribution and has potential to be applied over a much broader area as a regional marker bed. The large population and infrastructure proximal to Salak suggest that the unit should be considered in hazards assessments despite its age and the lack of subsequent similar eruptions.

Bulletin of Volcanology↗

USGS2021

Multidisciplinary constraints on magma compressibility, the pre-eruptive exsolved volatile fraction, and the H2O/CO2 molar ratio for the 2006 Augustine eruption, Alaska

Geodetically modeled reservoir volume changes during volcanic eruptions are commonly much smaller than the observed eruptive volumes. This discrepancy is thought to be partially due to the compressibility of magma, which is largely controlled by the presence of exsolved volatiles. The 2006 eruption of Augustine Volcano, Alaska, produced an eruptive volume that was ∼3 times larger than the geodetically estimated syn-eruptive subsurface volume change. In this study, we use a multistep methodology that combines constraints from geodetic, volcanic gas, geologic, and petrologic data together with equations relating physical processes to observable parameters. We apply a Monte Carlo approach to quantify uncertainties. Ultimately, we solve for the exsolved volatile volume fraction and the magma compressibility. We estimate Augustine's 2006 pre-eruptive exsolved volatile phase to be ∼5.5 vol% of the magma at storage depths, yielding a bulk magma compressibility of ∼3.8 × 10 −10 Pa −1 . We develop a novel approach to estimate the H 2 O/CO 2 ratio of the syn-eruptive gas emissions in the absence of direct H 2 O emission measurements which are hard to obtain due to the high background levels in ambient air. We find a best-fit H 2 O/CO 2 molar ratio of 29. We also investigate the effects of applying different equations of state to our model. We find that the Ideal Gas Law might be used as a first approximation due to its simplicity; however, it overestimates volatile density and compressibility significantly at storage depths. This project capitalizes on the insights that can be gained by integrating multidisciplinary data with models of physical processes.

Alaska↗

USGS2012

Phosphorus and groundwater: Establishing links between agricultural use and transport to streams

Phosphorus is a highly reactive element that is essential for life and forms a variety of compounds in terrestrial and aquatic ecosystems. In water, phosphorus may be present as the orthophosphate ion (PO 4 3- ) and is also present in all life forms as an essential component of cellular material. In natural ecosystems, phosphorus is derived from the erosion of rocks and is conserved for plant growth as it is returned to the soil through animal waste and the decomposition of plant and animal tissue; but in agricultural systems, a portion of the phosphorus is removed with each harvest, especially since phosphorus is concentrated in the seeds and fruit. Phosphorus is added to soil by using chemical fertilizers, manure, and composted materials. Agricultural use of chemical phosphorus fertilizer, in the United States, in 2008 was 4,247,000 tons, which is an increase of 25 percent since 1964 (http://www.ers.usda.gov/Data/FertilizerUse/). Widely grown corn, soybeans, and wheat use the greatest amount of phosphorus fertilizer among agricultural crops. Phosphorus is largely retained in soil by a process called adsorption. Soils have a limited capacity to store phosphorus, and once the capacity of soil to adsorb phosphorus is exceeded, the excess will dissolve and move more freely with water either directly to a stream or downward to an aquifer. Surface-water runoff from rainstorms or excess irrigation is the primary way that phosphorus or soil containing phosphorus is transported to streams in most watersheds. There is a growing awareness that long-term over-application of manure and chemical fertilizer contributes to phosphorus movement into the groundwater system, resulting in a significant groundwater source of phosphorus to streams and lakes, as well as potential contamination of the groundwater resources. Leaching of applied fertilizer and surface runoff of phosphorus from the soil can contribute to excess growth of algae in downstream water bodies, a condition known as eutrophication. Excessive amounts of algae in eutrophic water bodies can cause large daily changes in the amount of dissolved oxygen in the water because oxygen concentrations tend to be high during daylight hours as a result of photosynthetic activity but then decrease at night. Low concentrations of dissolved oxygen can stress or kill sensitive species living in the water. This study examined concentrations and movement of phosphorus in the soils and groundwater in five agricultural settings across the United States characterized by differences in soil geochemistry, climate, irrigation usage, and cropping systems to assess potential phosphorus movement in the soil and groundwater under common agricultural conditions. The study design included assessment of a variety of agricultural practices, especially cropping patterns and irrigation, so that the factors that contribute to phosphorus movement to groundwater, or sequestration of the phosphorus to soil could be compared and examined. This type of information could potentially be used to formulate best management practices to limit the transport of phosphorus from the agricultural fields.

Fact Sheet↗

USGS2013

Sediment geochemistry of Corte Madera Marsh, San Francisco Bay, California: have local inputs changed, 1830-2010?

Large perturbations since the mid-1800s to the supply and source of sediment entering San Francisco Bay have disturbed natural processes for more than 150 years. Only recently have sediment inputs through the Sacramento-San Joaquin Delta (the Delta) decreased to what might be considered pre-disturbance levels. Declining sediment inputs to San Francisco Bay raise concern about continued tidal marsh accretion, particularly if sea level rise accelerates in the future. The aim of this study is to explore whether the relative amount of local-watershed sediment accumulating in a tidal marsh has changed as sediment supply from the Sacramento-San Joaquin Rivers has decreased. To address this question, sediment geochemical indicators, or signatures, in the fine fraction (silt and clay) of Sacramento River, San Joaquin River, San Francisco Bay, and Corte Madera Creek sediment were identified and applied in sediment recovered from Corte Madera Marsh, one of the few remaining natural marshes in San Francisco Bay. Total major, minor, trace, and rare earth element (REE) contents of fine sediment were determined by inductively coupled plasma mass and atomic emission spectroscopy. Fine sediment from potential source areas had the following geochemical signatures: Sacramento River sediment downstream of the confluence of the American River was characterized by enrichments in chromium, zirconium, and heavy REE; San Joaquin River sediment at Vernalis and Lathrop was characterized by enrichments in thorium and total REE content; Corte Madera Creek sediment had elevated nickel contents; and the composition of San Francisco Bay mud proximal to Corte Madera Marsh was intermediate between these sources. Most sediment geochemical signatures were relatively invariant for more than 150 years, suggesting that the composition of fine sediment in Corte Madera Marsh is not very sensitive to changes in the magnitude, timing, or source of sediment entering San Francisco Bay through the Delta. Nor does there appear to be a ubiquitous increase in the proportion of fine sediment from Corte Madera watershed accumulating in the marsh during the last 20 years when sediment inflows through the Delta have decreased to pre-disturbance levels. We conclude that a large, well-mixed reservoir, such as the transportable fine sediment pool in San Francisco Bay, is the primary source of sediment to Corte Madera Marsh, and this source buffers the marsh against changes in sediment supply from the Delta and local watersheds. This study also found that Corte Madera Marsh sediment between about 10-30 centimeters depth is highly contaminated with lead, likely a legacy of lead smelter operations near Carquinez Strait and leaded gasoline use.

California↗

USGS2025

Geochemical processes related to mined, milled, or natural metal deposits in a rapidly changing global environment

The demand for metals and raw materials, such as nickel and copper, has been projected to expand in the coming decades, driven by the global energy transition, the need for green technologies, and expanding infrastructure. Consequently, the increasing extraction and production of mining waste can have adverse impacts on surrounding environments and human health. The aim of this thematic collection is to fill critical knowledge gaps in the present-day cycles of metal(loid)s from source to larger sinks, and the effect of environmental management, anthropogenic development, and climate change. Altogether, the studies have been conducted in different natural settings around the world and comprise investigations in laterites, a soil-medicinal plant system, watersheds, and banded iron formations, among others. The geochemical applications in tracing mineralization, its secondary products, and/or potential impact on the immediate environment are highly diverse with applied tools ranging from isotope tracers to major and trace element systematics. Particularly the use of rare earth elements, their patterns and anomalies are methods employed by several studies in this collection. We summarize the findings to offer a potential future direction for the use of geochemical tracing techniques in resource exploration in the context of climate change and environmental challenges.

Geochemistry: Exploration, Environment, Analysis↗

USGS2013

Whole-coal versus ash basis in coal geochemistry: a mathematical approach to consistent interpretations

Several standard methods require coal to be ashed prior to geochemical analysis. Researchers, however, are commonly interested in the compositional nature of the whole-coal, not its ash. Coal geochemical data for any given sample can, therefore, be reported in the ash basis on which it is analyzed or the whole-coal basis to which the ash basis data are back calculated. Basic univariate (mean, variance, distribution, etc.) and bivariate (correlation coefficients, etc.) measures of the same suite of samples can be very different depending which reporting basis the researcher uses. These differences are not real, but an artifact resulting from the compositional nature of most geochemical data. The technical term for this artifact is subcompositional incoherence. Since compositional data are forced to a constant sum, such as 100% or 1,000,000 ppm, they possess curvilinear properties which make the Euclidean principles on which most statistical tests rely inappropriate, leading to erroneous results. Applying the isometric logratio (ilr) transformation to compositional data allows them to be represented in Euclidean space and evaluated using traditional tests without fear of producing mathematically inconsistent results. When applied to coal geochemical data, the issues related to differences between the two reporting bases are resolved as demonstrated in this paper using major oxide and trace metal data from the Pennsylvanian-age Pond Creek coal of eastern Kentucky, USA. Following ilr transformation, univariate statistics, such as mean and variance, still differ between the ash basis and whole-coal basis, but in predictable and calculated manners. Further, the stability between two different components, a bivariate measure, is identical, regardless of the reporting basis. The application of ilr transformations addresses both the erroneous results of Euclidean-based measurements on compositional data as well as the inconsistencies observed on coal geochemical data reported on different bases.

International Journal of Coal Geology↗

USGS2009

Implications of estimated magmatic additions and recycling losses at the subduction zones of accretionary (non-collisional) and collisional (suturing) orogens

Arc magmatism at subduction zones (SZs) most voluminously supplies juvenile igneous material to build rafts of continental and intra-oceanic or island arc (CIA) crust. Return or recycling of accumulated CIA material to the mantle is also most vigorous at SZs. Recycling is effected by the processes of sediment subduction, subduction erosion, and detachment and sinking of deeply underthrust sectors of CIA crust. Long-term (>10-20 Ma) rates of additions and losses can be estimated from observational data gathered where oceanic crust underruns modern, long-running (Cenozoic to mid-Mesozoic) ocean-margin subduction zones (OMSZs, e.g. Aleutian and South America SZs). Long-term rates can also be observationally assessed at Mesozoic and older crust-suturing subduction zone (CSSZs) where thick bodies of CIA crust collided in tectonic contact (e.g. Wopmay and Appalachian orogens, India and SE Asia). At modern OMSZs arc magmatic additions at intra-oceanic arcs and at continental margins are globally estimated at c. 1.5 AU and c. 1.0 AU, respectively (1 AU, or Armstrong Unit,= 1 km 3 a -1 of solid material). During collisional suturing at fossil CSSZs, global arc magmatic addition is estimated at 0.2 AU. This assessment presumes that in the past the global length of crustal collision zones averaged c. 6000 km, which is one-half that under way since the early Tertiary. The average long-term rate of arc magmatic additions extracted from modern OMSZs and older CSSZs is thus evaluated at 2.7 AU. Crustal recycling at Mesozoic and younger OMSZs is assessed at c. 60 km 3 Ma -1 km -1 (c. 60% by subduction erosion). The corresponding global recycling rate is c. 2.5 AU. At CSSZs of Mesozoic, Palaeozoic and Proterozoic age, the combined upper and lower plate losses of CIA crust via subduction erosion, sediment subduction, and lower plate crustal detachment and sinking are assessed far less securely at c. 115 km 3 Ma -1 km -1 . At a global length of 6000 km, recycling at CSSZs is accordingly c. 0.7 AU. The collective loss of CIA crust estimated for modern OMSZs and for older CSSZs is thus estimated at c. 3.2 AU. SZ additions (2.7 AU) and subtractions (23.2 AU) are similar. Because many uncertainties and assumptions are involved in assessing and applying them to the deep past, the net growth of CIA crust during at least Phanerozoic time is viewed as effectively nil. With increasing uncertainty, the long-term balance can be applied to the Proterozoic, but not before the initiation of the present style of subduction at c. 3 Ga. Allowing that since this time a rounded-down rate of recycling of 3 AU is applicable, a startlingly high volume of CIA crust equal to that existing now has been recycled to the mantle. Although the recycled volume (c. 9 ?? 10 9 km 3 ) is small (c. 1%) compared with that of the mantle, it is large enough to impart to the mantle the signature of recycled CIA crust. Because subduction zones are not spatially fixed, and their average global lengths have episodically been less or greater than at present, recycling must have contributed significantly to creating recognized heterogeneities in mantle geochemistry. ?? The Geological Society of London 2009.

Geological Society Special Publication↗

USGS2006

Effect of bedrock permeability on subsurface stormflow and the water balance of a trenched hillslope at the Panola Mountain Research Watershed, Georgia, USA

The effect of bedrock permeability on subsurface stormflow initiation and the hillslope water balance is poorly understood. Previous hillslope hydrological studies at the Panola Mountain Research Watershed (PMRW), Georgia, USA, have assumed that the bedrock underlying the trenched hillslope is effectively impermeable. This paper presents a series of sprinkling experiments where we test the bedrock impermeability hypothesis at the PMRW. Specifically, we quantify the bedrock permeability effects on hillslope subsurface stormflow generation and the hillslope water balance at the PMRW. Five sprinkling experiments were performed by applying 882-1676 mm of rainfall over a ???5.5 m ?? 12 m area on the lower hillslope during ???8 days. In addition to water input and output captured at the trench, we measured transpiration in 14 trees on the slope to close the water balance. Of the 193 mm day-1 applied during the later part of the sprinkling experiments when soil moisture changes were small, < 14 mm day-1 was collected at the trench and <4 mm day-1 was transpired by the trees, with residual bedrock leakage of > 175 mm day-1 (91%). Bedrock moisture was measured at three locations downslope of the water collection system in the trench. Bedrock moisture responded quickly to precipitation in early spring. Peak tracer breakthrough in response to natural precipitation in the bedrock downslope from the trench was delayed only 2 days relative to peak tracer arrival in subsurface stormflow at the trench. Leakage to bedrock influences subsurface stormflow at the storm time-scale and also the water balance of the hillslope. This has important implications for the age and geochemistry of the water and thus how one models this hillslope and watershed. Copyright ?? 2006 John Wiley & Sons, Ltd.

Hydrological Processes↗

USGS2016

The geochemical atlas of Alaska, 2016

A rich legacy of geochemical data produced since the early 1960s covers the great expanse of Alaska; careful treatment of such data may provide significant and revealing geochemical maps that may be used for landscape geochemistry, mineral resource exploration, and geoenvironmental investigations over large areas. To maximize the spatial density and extent of data coverage for statewide mapping of element distributions, we compiled and integrated analyses of more than 175,000 sediment and soil samples from three major, separate sources: the U.S. Geological Survey, the National Uranium Resource Evaluation program, and the Alaska Division of Geological & Geophysical Surveys geochemical databases. Various types of heterogeneity and deficiencies in these data presented major challenges to our development of coherently integrated datasets for modeling and mapping of element distributions. Researchers from many different organizations and disparate scientific studies collected samples that were analyzed using highly variable methods throughout a time period of more than 50 years, during which many changes in analytical techniques were developed and applied. Despite these challenges, the U.S. Geological Survey has produced a new systematically integrated compilation of sediment and soil geochemical data with an average sample site density of approximately 1 locality per 10 square kilometers (km 2 ) for the entire State of Alaska, although density varies considerably among different areas. From that compilation, we have modeled and mapped the distributions of 68 elements, thus creating an updated geochemical atlas for the State.

Alaska↗