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USGS1982

Effects of effluent spray irrigation on ground water at a test site near Tarpon Springs, Florida

Secondary-treated effluent was applied to a 7.2-acre test site near Tarpon Springs, Fla., for about 1 year at an average rate of 0.06 million gallons per day and 3 years at 0.11 million gallons per day. Chemical fertilizer was applied periodically to the test site and adjacent areas. Periodic mounding of the water table occurred due to effluent irrigation, inducing radial flow from the test site. Physical, geochemical, biochemical processes effectively reduced total nitrogen concentration 90% and total phosphorous concentration more than 95% in the ground water of the surficial aquifer about 300 feet downgradient from the test site from that of the applied effluent. Downgradient, total nitrogen averaged 2.4 milligrams per liter and total phosphorus averaged 0.17 milligrams per liter. Substantial increases in total phosphorus were observed when the pH of the ground water increased. Total coliform bacteria in the ground water of the surficial aquifer were generally less than 100 colonies per 100 milliliters. Fecal coliform bacteria were generally less than 25 colonies per 100 milliliters at the test site and were not detected downgradient or near the test site. Fecal streptococcal bacteria were generally less than 100 colonies per 100 milliliters at the test site, but were detected on three occasions near the test site. (USGS)

Open-File Report↗

USGS2013

Defining groundwater age

This book investigates applications of selected chemical and isotopic substances that can be used to recognize and interpret age information pertaining to ‘old’ groundwater (defined as water that was recharged on a timescale from approximately 1000 to more than 1 000 000 a). However, as discussed below, only estimates of the ‘age’ of water extracted from wells can be inferred. These groundwater age estimates are interpreted from measured concentrations of chemical and isotopic substances in the groundwater. Even then, there are many complicating factors, as discussed in this book. In spite of these limitations, much can be learned about the physics of groundwater flow and about the temporal aspects of groundwater systems from age interpretations of measured concentrations of environmental tracers in groundwater systems. This chapter puts the concept of ‘age’ into context, including its meaning and interpretation, and attempts to provide a unifying usage for the rest of the book.

Book chapter↗

USGS2019

Return flows from beaver ponds enhance floodplain-to-river metals exchange in alluvial mountain catchments

River to floodplain hydrologic connectivity is strongly enhanced by beaver- ( Castor canadensis ) engineered channel water diversions. The hydroecological impacts are wide ranging and generally positive, however, the hydrogeochemical characteristics of beaver-induced flowpaths have not been thoroughly examined. Using a suite of complementary ground- and drone-based heat tracing and remote sensing methodology we characterized the physical template of beaver-induced floodplain exchange for two alluvial mountain streams near Crested Butte, Colorado, USA. A flowpath-oriented perspective to water quality sampling allowed characterization of the chemical evolution of channel water diverted through floodplain beaver ponds and ultimately back to the channel in ‘beaver pond return flows’. Subsurface return flow seepages were universally suboxic, while ponds and surface return flows showed a range of oxygen concentration due to in-situ photosynthesis and atmospheric mixing. Median concentrations of reduced metals: manganese (Mn), iron (Fe), aluminum (Al), and arsenic (As) were substantially higher along beaver-induced flowpaths than in geologically controlled seepages and upstream main channel locations. The areal footprint of reduced return seepage flowpaths were imaged with surface electromagnetic methods, indicating extensive zones of high-conductivity shallow groundwater flowing back toward the main channels and emerging at relatively warm bank seepage zones observed with infrared. Multiple-depth redox dynamics within one focused seepage zone showed coupled variation over time, likely driven by observed changes in seepage rate that may be controlled by pond stage. High-resolution times series of dissolved Mn and Fe collected downstream of the beaver-impacted reaches demonstrated seasonal dynamics in mixed river metal concentrations. Al time series concentrations showed proportional change to Fe at the smaller stream location, indicating chemically reduced flowpaths were sourcing Al to the channel. Overall our results indicated beaver-induced floodplain exchanges create important, and perhaps dominant, transport pathways for floodplain metals by expanding chemically-reduced zones paired with strong advective exchange.

Colorado↗

USGS1975

Origin of magnetite and pyrrhotite in carbonaceous chondrites

CARBONACEOUS chondrites, although comprising only about 2% of known meteorites, are extremely interesting for scientific investigation. Their mineral constitution, and the correspondence between their bulk chemical composition and the solar abundance of condensable elements, indicate that minimum chemical fractionation and thermal alteration have occurred. The mineral phases observed in these primitive chondrites are sufficiently unique, with respect to other meteorite classes, to have elicited considerable speculation about the physical environment in which they formed 1–7 .

Nature↗

USGS2001

Water Resources Data, New Jersey, Water Year 2000. Volume 3. Water-Quality Data

Water-resources data for the 2000 water year for New Jersey are presented in three volumes, and consist of records of stage, discharage, and quality of streams; stage and contents of lakes and reservoirs; and levels and quality of ground water. Volume 3 contains a summary of surface and ground water hydrologic conditions for the 2000 water year, a listing of current water-resource projects in New Jersey, a bibliography of water-related reports, articles, and fact sheets for New Jersey completed by the Geological Survey in recent years, water-quality records of chemical analyses from 125 continuing-record surface-water stations, 62 miscellaneous surface-water sites, 73 ground-water sites, and records of daily statistics of temperature and other physical measurements from 45 continuous-recording stations. Locations of water-quality stations are shown in figures 18-20. Locations of miscellaneous water-quality sites are shown in figures 11 and 42-49. These data represent that part of the National Water Data System operated by the U.S. Geological Survey and cooperating Federal, State, and local agencies in New Jersey.

Water Data Report↗

USGS2010

Regional and grain size influences on the geochemistry of soil at Gusev Crater

Congruous with earlier work, Martian soil along the Spirit Rover's traverse at Gusev crater can be divided into three broad groups by size: fines (<150 μ m), sand, and a mix of various grain sizes. The key chemical observation is greater homogeneity in fines relative to the other two, consistent with regional‐ and global‐scale sampling of chemical compositions by finer particle sizes. The mix class is generally more heterogeneous as are samples from the Columbia Hills within each class. Variation in the trace element Ni is consistent with a CI contribution not exceeding 3%, while that of Ti is compatible with Fe‐Ti oxide enrichment not exceeding 3%. Physical mixing models are poorly supported. Among many potential binary and three‐component mixing models, only two show some consistency with the soil data: typical fines with the opaline Si end‐member identified at Home Plate and typical fines with sulfates (bearing a variable mix of Ca, Fe, and Mg cations). We also infer that binary mixing transcends classes, contrasting strongly with terrestrial sediments, and that mixing trends are consistent with significant nonmixing contributions, perhaps including localized chemical alteration. The decoupling between chemistry and grain size classes also suggests that processes linking composition with grain size, such as heavy mineral sorting, may have been minimal or absent entirely. The primary exception to this is the correlation between Cl and Si, Cl‐S, and Al‐Si, which is strongest in the fines class.

Journal of Geophysical Research E: Planets↗

USGS2013

U.S. Geological Survey environmental health science strategy — Providing environmental health science for a changing world

Executive Summary America has an abundance of natural resources. We have bountiful clean water, fertile soil, and unrivaled national parks, wildlife refuges, and public lands. These resources enrich our lives and preserve our health and wellbeing. These resources have been maintained because of our history of respect for their value and an enduring commitment to their vigilant protection. Awareness of the social, economic, and personal value of the health of our environment is increasing. The emergence of environmentally driven diseases caused by exposure to contaminants and pathogens is a growing concern worldwide. New health threats and patterns of established threats are affected by both natural and anthropogenic changes to the environment. Human activities are key drivers of emerging (new and re-emerging) health threats. Societal demands for land and natural resources, quality of life, and economic prosperity lead to environmental change. Natural earth processes, climate trends, and related climatic events will compound the environmental impact of human activities. These environmental drivers will influence exposure to disease agents, including viral, bacterial, prion, and fungal pathogens, parasites, synthetic chemicals and substances, natural earth materials, toxins, and other biogenic compounds. The U.S. Geological Survey (USGS) defines environmental health science broadly as the interdisciplinary study of relations among the quality of the physical environment, the health of the living environment, and human health. The interactions among these three spheres are driven by human activities, ecological processes, and natural earth processes; the interactions affect exposure to contaminants and pathogens and the severity of environmentally driven diseases in animals and people. This definition provides USGS with a framework for synthesizing natural science information from across the Bureau and providing it to environmental, natural resource, agricultural, and public health managers. USGS specializes in science at the environment-health interface, by characterizing the processes that affect the interaction among the physical environment, the living environment, and people, and the resulting factors that affect ecological and human exposure to disease agents. The USGS is a Federal science agency with a broad range of natural science expertise relevant to environmental health. USGS provides scientific information and tools as a scientific basis for management and policy decisionmaking. This report describes a 10-year strategy that encompasses the portfolio of USGS environmental health science. It summarizes national environmental health priorities that USGS is best suited to address, and will serve as a strategic framework for USGS environmental health science goals, actions, and outcomes for the next decade. Implementation of this strategy is intended to aid coordination of USGS environmental health activities and to provide a focal point for disseminating information to stakeholders. The “One Health” paradigm advocated by the World Health Organization (WHO; World Health Organization, 2011), and the American Veterinary Medical Association (AVMA; American Veterinary Medical Association, 2008), among others, is based on a general recognition that the health of humans, animals, and the environment are inextricably linked. Thus, successful efforts to protect that health will require increased interdisciplinary research and increased communication and collaboration among the broader scientific and health community. This strategy is built upon that paradigm.

Circular↗

USGS2021

Hydrographic and benthic mapping—St. Croix National Scenic Riverway—Osceola landing

High-resolution topographic and bathymetric mapping can assist in the analysis of river habitat. The National Park Service has been planning to relocate a boat ramp along the St. Croix River in Minnesota, across the river from the town of Osceola, Wisconsin, to improve visitor safety, improve operations for commercial use, enhance the overall visitor experience, and eliminate deferred maintenance at the landing. This landing grants access to the St. Croix River, which is a part of the National Park Service St. Croix National Scenic Riverway. Hydrographic and topographic surveys were needed to determine where the new location should be. The objective for these surveys was to provide baseline information in order to assess the direct effects of the landing relocation on physical habitat in areas adjacent to Osceola, Wisconsin. The study area for these surveys was about 18.5 hectares and located directly off the existing landing. Although the existing boat launch is referred to as the Osceola landing, it is located on the Minnesota side of the river and is the busiest National Park Service landing on the St. Croix River (National Park Service St. Croix National Scenic Riverway, 2020). This report documents methods and results of aquatic benthic mapping in a small area of the St. Croix River. The hydroacoustic and topographic surveys were collected from October 16–17, 2019. The hydrographic surveys consisted of multibeam and sidescan sound navigation and ranging (sonars). The topographic shoreline survey consisted of light detection and ranging (lidar) captured by boat adjacent to riverbanks. Additionally, an acoustic Doppler current profiler was used to measure flow velocities. The water level was higher than normal, and therefore had faster flow during the hydroacoustic surveys. Multibeam, lidar, and sidescan surveys occurred the first day, and the velocity mapping and ground truthing was conducted the second day. Multibeam and lidar provided derivative datasets that included bathymetry and a topobathy with a spatial resolution of 1 foot. From these data, additional data could be measured including slope and terrain ruggedness. Sidescan (acoustic reflectance measures) provided imagery that was used to help with interpretation of the river bottom. Outcomes from these combined datasets were substrate and bedform maps. Much of the area was covered in sand ripples or small dunes. A small area running adjacent to the deeper valley or cut down the river consisted of harder substrates, such as cobble and gravel. Large woody debris piles were found throughout the study area. Multiple stationary moving-bed tests were completed, and no corrections were recommended for the conditions occurring during survey. Mussel presence was noted in some of the underwater videos. The physical parameters of depth, flow, bedforms, and substrate derived from the datasets provided baseline measures for a benthic habitat map. Further analysis of benthic habitat might be possible with additional biological and chemical data.

Wisconsin↗

USGS2023

Data summary report: Unregulated contaminants monitoring project

The Drinking Water Protection Section of the Minnesota Department of Health conducted reconnaissance monitoring of selected public water systems in Minnesota. Funding was obtained primarily from the Environment and Natural Resources Trust Fund. Sampling was conducted in 2019 and 2021. Laboratory analysis of samples was conducted for a variety of different contaminants of emerging concern (CECs), including selected pharmaceuticals, pesticides, PFAS, wastewater indicators and other parameters chosen for the physical and land use setting surrounding the sampling points. Sampling site and parameter selection were designed with several goals, as follows: Characterize occurrence and distribution of selected CECs in settings where such chemicals are most likely to be present; Determine if any such occurrences represent a public health concern; Compare results from coupled source water and finished (i.e., treated) water samples at public water system sites where such sampling is feasible; Assess if results from geologically vulnerable (sensitive subject to rapid recharge) and geologically non-vulnerable settings differ significantly. 306 samples were collected as part of the study, from three networks of public water systems differentiated on the basis of source water type (i.e., surface water or groundwater) and land use environment (agricultural and wastewater influenced). This report provides a preliminary, qualitative evaluation of the results. Additionally, more rigorous research will be conducted on these water quality data to evaluate the below findings in more detail. High-level findings from this assessment include the following: Very few samples exceeded health-based guidance for CECs; o When this occurred, MDH staff conducted follow up sampling at the system and provided technical advice about managing the situation. Only a fraction of the CECs analyzed were detected; o Of the 522 different CECs analyzed in the water samples, 161 were detected in one or more samples; o Additionally, most detections were at low levels; Among the CEC classes included in the analytical work, pesticides and PFAS were generally detected at a greater frequency than other CECs; o See Executive Summary Figure 1. The ten most commonly detected individual compounds include: o Tribromomethane, or bromoform, (a disinfection by-product) (70% of sites where analyzed); o norgestrel (a pharmaceutical) (69% of sites where analyzed); o lithium (68% of sites where analyzed); o Metolachlor SA (52%), Deethylatrazine (49%), atrazine (45%), and deisopropylatrazine (31%) (pesticides); o PFBA (44%) and PFHxS (27%) (PFAS compounds); and o 5-methyl benzotriazole (29%) (a benzotriazole). Some CECs were detected more frequently in samples collected from surface waters than those collected from groundwater sources; CEC concentrations were generally higher in vulnerable settings compared to nonvulnerable settings; Whether CECs were detected more frequently in the source water or finished water varied by CEC class. For example, o Benzotriazoles and pharmaceuticals were more frequently detected in source water samples than finished water samples; and o Tribromomethane, or bromoform, a common disinfection by-product, was more frequently found in finished water samples than in source water samples. This work prompted a series of programmatic changes and innovations: A response framework was established for helping the program and public water systems manage detections of unregulated CECs in drinking water; Results were forwarded to the program within MDH responsible for developing healthbased guidance in order to nominate specific compounds found in drinking water but for which limited or no risk advice is available; MDH is seeking support from the Clean Water Council to support the establishment of permanent capacity within the Drinking Water Protection Section to continue sampling efforts of this type.

Minnesota↗

USGS1987

Changes in the H O Ar isotope composition of clays during retrograde alteration

K-Ar ages of illite alteration associated with Middle Proterozoic Athabasca unconformity-type U deposits in Saskatchewan range from 414 to 1493 Ma. The K-Ar ages correlate with water contents and δD values such that illites with young K-Ar ages have δD values as low as −169 and water contents as high as 7.7 wt.% whereas illites with older ages have δD values near −70 and water contents near 4 wt.%. Water extracted at 400°C from illites with low δD values and high water contents has low δD and δ 18 O values similar to those of modern meteoric water suggesting that some of the illites associated with the original deposition of the ore underwent varying degrees of retrograde alteration. The alteration is initiated by hydration of sites in the interlayer region of the illite which results in the partial resetting of the K-Ar ages and introduction of excess structural water in the form of interlamellar water. The interlamellar water is enriched in 18 O by about 7 per mil relative to the water that physically surrounded the clay particle. Further alteration decreases the δD value and increases the δ 18 O value of the illite by isotopic exchange between the mineral and the interlamellar water. Although the chemical compositions and XRD patterns of the altered illites indicate that no detectable smectite component is present in the samples, the isotopic results suggest that the altered illites may be an early precursor in the formation of mixed-layer illite/smectite by retrograde alteration of pure illite. The wide variation of δD values of chlorite and kaolinite from these U deposits is analogous to that of the illite suggesting that retrograde alteration of clays by meteoric water can be substantial. The general association of altered clays with areas containing the highest concentrations of U is probably related to localized permeability within the ore zone.

Geochimica et Cosmochimica Acta↗

USGS2007

A simulation-based approach for estimating premining water quality: Red Mountain Creek, Colorado

Regulatory agencies are often charged with the task of setting site-specific numeric water quality standards for impaired streams. This task is particularly difficult for streams draining highly mineralized watersheds with past mining activity. Baseline water quality data obtained prior to mining are often non-existent and application of generic water quality standards developed for unmineralized watersheds is suspect given the geology of most watersheds affected by mining. Various approaches have been used to estimate premining conditions, but none of the existing approaches rigorously consider the physical and geochemical processes that ultimately determine instream water quality. An approach based on simulation modeling is therefore proposed herein. The approach utilizes synoptic data that provide spatially-detailed profiles of concentration, streamflow, and constituent load along the study reach. This field data set is used to calibrate a reactive stream transport model that considers the suite of physical and geochemical processes that affect constituent concentrations during instream transport. A key input to the model is the quality and quantity of waters entering the study reach. This input is based on chemical analyses available from synoptic sampling and observed increases in streamflow along the study reach. Given the calibrated model, additional simulations are conducted to estimate premining conditions. In these simulations, the chemistry of mining-affected sources is replaced with the chemistry of waters that are thought to be unaffected by mining (proximal, premining analogues). The resultant simulations provide estimates of premining water quality that reflect both the reduced loads that were present prior to mining and the processes that affect these loads as they are transported downstream. This simulation-based approach is demonstrated using data from Red Mountain Creek, Colorado, a small stream draining a heavily-mined watershed. Model application to the premining problem for Red Mountain Creek is based on limited field reconnaissance and chemical analyses; additional field work and analyses may be needed to develop definitive, quantitative estimates of premining water quality.

Colorado↗

USGS2010

Water-quality, water-level, and discharge data associated with the Mississippi embayment agricultural chemical-transport study, 2006-2008

In 2006, the Agricultural Chemicals: Sources, Transport and Fate study team (Agricultural Chemicals Team, ACT) of the U.S. Geological Survey National Water-Quality Assessment Program began a study in northwestern Mississippi to evaluate the influence of surface-water recharge on the occurrence of agriculturally related nutrients and pesticides in the Mississippi River Valley alluvial aquifer. The ACT study was composed in the Bogue Phalia Basin, an indicator watershed within the National Water-Quality Assessment Program Mississippi Embayment Study Unit and utilized several small, subbasins within the Bogue Phalia to evaluate surface and groundwater interaction and chemical transport in the Basin. Data collected as part of this ACT study include water-quality data from routine and incident-driven water samples evaluated for major ions, nutrients, organic carbon, physical properties, and commonly used pesticides in the area; discharge, gage height and water-level data for surface-water sites, the shallow alluvial aquifer, and hyporheic zone; additionally, agricultural data and detailed management activities were reported by land managers for farms within two subbasins of the Bogue Phalia Basin—Tommie Bayou at Pace, MS, and an unnamed tributary to Clear Creek near Napanee, MS.

Mississippi↗

USGS1977

Hydraulic conductivity and water quality of the shallow aquifer, Palm Beach County, Florida

Subsurface geophysical logs were correlated with logs of drill cuttings to determine the permeability of selected zones of the shallow aquifer, Palm Beach County, Fla. The hydraulic conductivity of the aquifer is estimated to range from 1 to 130 feet per day, based on lithology and physical properties. The yield of wells penetrating this aquifer ranges from 100 to more than 1,000 gallons per minute. Water samples were collected from different depths throughout the county and analyzed for chemical constituents. Stiff diagrams illustrate the changes in types of water by depth and area. Water of suitable quality is in the eastern parts of the county. In this area the aquifer is the thickest and most permeable. The concentration of chemical constituents in the water increase in a westerly direction. The water in the western parts of the county is unsuitable for most purposes. (Woodard-USGS)

Florida↗

USGS2017

Zirconium and hafnium

Zirconium and hafnium are corrosion-resistant metals that are widely used in the chemical and nuclear industries. Most zirconium is consumed in the form of the main ore mineral zircon (ZrSiO 4 , or as zirconium oxide or other zirconium chemicals. Zirconium and hafnium are both refractory lithophile elements that have nearly identical charge, ionic radii, and ionic potentials. As a result, their geochemical behavior is generally similar. Both elements are classified as incompatible because they have physical and crystallochemical properties that exclude them from the crystal lattices of most rock-forming minerals. Zircon and another, less common, ore mineral, baddeleyite (ZrO 2 ), form primarily as accessory minerals in igneous rocks. The presence and abundance of these ore minerals in igneous rocks are largely controlled by the element concentrations in the magma source and by the processes of melt generation and evolution. The world’s largest primary deposits of zirconium and hafnium are associated with alkaline igneous rocks, and, in one locality on the Kola Peninsula of Murmanskaya Oblast, Russia, baddeleyite is recovered as a byproduct of apatite and magnetite mining. Otherwise, there are few primary igneous deposits of zirconium- and hafnium-bearing minerals with economic value at present. The main ore deposits worldwide are heavy-mineral sands produced by the weathering and erosion of preexisting rocks and the concentration of zircon and other economically important heavy minerals, such as ilmenite and rutile (for titanium), chromite (for chromium), and monazite (for rare-earth elements) in sedimentary systems, particularly in coastal environments. In coastal deposits, heavy-mineral enrichment occurs where sediment is repeatedly reworked by wind, waves, currents, and tidal processes. The resulting heavy-mineral-sand deposits, called placers or paleoplacers, preferentially form at relatively low latitudes on passive continental margins and supply 100 percent of the world’s zircon. Zircon makes up a relatively small percentage of the economic heavy minerals in most deposits and is produced primarily as a byproduct of heavy-mineral-sand mining for titanium minerals. From 2003 to 2012, world zirconium mineral concentrates production increased by more than 40 percent, and Australia and South Africa were the leading producers. Global consumption of zirconium mineral concentrates generally increased during the same time period, largely as a result of increased demand in developing economies in Asia and the Middle East. Global demand weakened in 2012, causing a decrease in world production of zirconium mineral concentrates and delaying the development of several new mining projects. Global consumption is expected to increase in the future, however, as demand from the ceramics, chemicals, and metals industries increases (driven by renewed growth in developing economies) and demand for zirconium and hafnium metal increases (driven by the construction and operation of new nuclear powerplants). The behaviors of zirconium and hafnium in the environment are very similar to one another in that most zirconium- and hafnium-bearing minerals have limited solubility and reactivity. Anthropogenic sources of zirconium, and likely hafnium, are from industrial zirconium-containing byproducts and emissions from the processing of sponge zirconium, and exposure to the general population from these sources is small. Zirconium and hafnium are likely not essential to human health and generally are considered to be of low toxicity to humans. The main exposure risks are associated with industrial inhalation and dermal exposure. Because of the low solubility of zirconium and hafnium, ecological health concerns in the aquatic environment and in soils are minimal. Heavy-mineral-sand mining may lead to increased erosion rates when the mining is managed improperly. In addition, surface mining requires removal of the overlying organic soil layer and produces waste material that includes tailings and slimes. The soil removal and mining activity disturbs the surrounding ecosystem and alters the character of the landscape. Dry mineral separation processes create high amounts of airborne dust, whereas wet mineral separation processes do not. In operations that restore the landscape to pre-mining conditions, the volume of waste and the impact on the landscape may be relatively temporary.

Professional Paper↗

USGS1925

The evolution and disintegration of matter

In any attempt to study the evolution of matter it is necessary to begin with its simplest known forms, the so-called chemical elements. During a great part of the nineteenth century many philosophical chemists held a vague belief that these elements were not distinct entities but manifestations of one primal substance-the protyle, as it is sometimes called. Other chemists, more conservative, looked askance at all such speculations and held fast to what they regarded as established facts. To them an element was something distinct from other kinds of matter, a substance which could neither be decomposed nor transmuted into anything else. This belief, however, was based entirely upon negative evidence-the inadequacy of our existing resources to produce such sweeping changes. Many important facts were ignored, and especially the fact that the elements are connected by very intimate relations, such as are best shown in the periodic law of Mendeleef, who, from gaps in his table of atomic weights, predicted the existence of three unknown metals, which have since been discovered. For these metals, scandium, gallium, and germanium, he foretold not only their atomic weights but also their most characteristic physical properties and the sort of compounds that each one would form. His prophecies have been verified in every essential particular. One obvious conclusion was soon drawn from Mendeleef's "law," although he was too cautious to admit it, namely, that the chemical elements must have had some community of origin. The philosophical speculations as to their nature were fully justified.

Professional Paper↗

USGS2000

Mineralogic and compositional properties of Martian soil and dust: results from Mars Pathfinder

Mars Pathfinder obtained multispectral, elemental, magnetic, and physical measurements of soil and dust at the Sagan Memorial Station during the course of its 83 sol mission. We describe initial results from these measurements, concentrating on multispectral and elemental data, and use these data, along with previous Viking, SNC meteorite, and telescopic results, to help constrain the origin and evolution of Martian soil and dust. We find that soils and dust can be divided into at least eight distinct spectral units, based on parameterization of Imager for Mars Pathfinder (IMP) 400 to 1000 nm multispectral images. The most distinctive spectral parameters for soils and dust are the reflectivity in the red, the red/blue reflectivity ratio, the near-IR spectral slope, and the strength of the 800 to 1000 nm absorption feature. Most of the Pathfinder spectra are consistent with the presence of poorly crystalline or nanophase ferric oxide(s), sometimes mixed with small but varying degrees of well-crystalline ferric and ferrous phases. Darker soil units appear to be coarser-grained, compacted, and/or mixed with a larger amount of dark ferrous materials relative to bright soils. Nanophase goethite, akaganeite, schwertmannite, and maghemite are leading candidates for the origin of the absorption centered near 900 nm in IMP spectra. The ferrous component in the soil cannot be well-constrained based on IMP data. Alpha proton X-ray spectrometer (APXS) measurements of six soil units show little variability within the landing site and show remarkable overall similarity to the average Viking-derived soil elemental composition. Differences exist between Viking and Pathfinder soils, however, including significantly higher S and Cl abundances and lower Si abundances in Viking soils and the lack of a correlation between Ti and Fe in Pathfinder soils. No significant linear correlations were observed between IMP spectral properties and APXS elemental chemistry. Attempts at constraining the mineralogy of soils and dust using normative calculations involving mixtures of smectites and silicate and oxide minerals did not yield physically acceptable solutions. We attempted to use the Pathfinder results to constrain a number of putative soil and dust formation scenarios, including palagonitization and acid-fog weathering. While the Pathfinder soils cannot be chemically linked to the Pathfinder rocks by palagonitization, this study and McSween et al. [1999] suggest that palagonitic alteration of a Martian basaltic rock, plus mixture with a minor component of locally derived andesitic rock fragments, could be consistent with the observed soil APXS and IMP properties.

Journal of Geophysical Research E: Planets↗

USGS2000

Water Resources Data - New Jersey, Water Year 1999, Volume 3, Water-Quality Data

Water-resources data for the 1999 water year for New Jersey are presented in three volumes, and consists of records of stage, discharge, and water quality of streams; stage and contents of lakes and reservoirs; and water levels and water quality of ground water. Volume 3 contains a summary of surface and ground water hydrologic conditions for the 1999 water year, a listing of current water-resource projects in New Jersey, a bibliography of water-related reports, articles, and fact sheets for New Jersey completed by the Geological Survey in recent years, water-quality records of chemical analyses from 133 surface-water stations, 46 miscellaneous surface-water sites, 30 ground-water stations, 41 miscellaneous ground-water sites, and records of daily statistics of temperature and other physical measurements from 17 continuous-monitoring stations. Locations of water-quality stations are shown in figures 11 and 17-20. Locations of miscellaneous water-quality sites are shown in figures 29-32 and 34. These data represent the part of the National Water Data System operated by the U.S. Geological Survey and cooperating Federal, State, and local agencies in New Jersey.

Water Data Report↗

USGS1983

Preliminary assessment of the geochemistry and mineral favorability of the postorogenic granites of the southeastern Arabian Shield, Kingdom of Saudi Arabia

Chemical analyses of samples for 19 postorogenic plutons from the southeastern Arabian Shield show that these rocks have average potassium/rubidium ratios (162) and average rubidium/strontium ratios (11.8) characteristic of highly evolved granites. Most of the analyzed samples are peraluminous. Three plutons are physically similar in terms of shape and megascopic textural zonation to peralkaline complexes in the northeastern part of the Shield, but none of the samples from these plutons is peralkaline. However, these plutons do contain the least-evolved samples. Zinc, yttrium, uranium, thorium, and possibly copper, each occur in anomalously high concentrations in at least one pluton relative to contents typically cited for granite. The average regional concentrations of copper and zinc are anomalously high. These facts suggest at least a moderate potential for mineralization in the southeastern part of the Shield. Good correlations (r of 0.5 to 0.8) between uranium, thorium, yttrium, and rubidium and an excellent correlation (r=0.98) between uranium and radium-equivalent uranium suggest that secondary deposits of these elements are unlikely and that magmatic deposits, especially of a pegmatitic nature, are more likely. Concentrations of some major elements and several trace elements covary with sample location as measured by latitude and longitude. This fact is interpreted to reflect regional variations in the protolith that have been proposed on the basis of lead isotopic data. The chemical variations suggest a largely oceanic crustal component for granites in the southwestern part of the southeastern Shield and a largely continental crustal component to the northeast. Further quantitative analysis is recommended to verify and accurately delineate anomalous concentrations of trace elements. Trend surface analysis of all available data for postorogenic granites from the eastern Arabian Shield is suggested as a method for testing regional variations in the protolith that might control locations of highly favorable areas of ore deposition.

Open-File Report↗