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Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

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At least 55 records · Page 3Linked to original sources
USGS1975

Impacts of chemicals on waterfowl reproduction and survival

Residues of organochlorine pesticides, PCB's, heavy metals, and other toxic chemicals are ubiquitous in the biosphere and are commonly found in tissues and eggs of wild birds. This paper reviews research on the effects of these chemicals, with particular reference to waterfowl. Extensive mortality of waterfowl has occurred in the Gulf Coast region as a result of ingestion of aldrin-treated rice seed. Populations of fulvous tree ducks (Dendrocygna bicolor) have declined in recent years in that area. DDE impaired reproduction of both mallards (Anas platyrhynchos) and black ducks (Arias rubripes) in experimental studies, resulting in thin shells, cracked eggs, and poor hatching success. Eggs incubated by the hens broke and cracked more frequently than those in incubators. In the field, residues are higher in ducks that feed on animal material than in vegetarians; differences are pronounced both geographically and among species. Mercury at levels that occur in certain heavily polluted areas in the United States and Canada has, in experimental studies, lowered the reproductive success of mallards and black ducks and reduced the survival of ducklings. Oil spills have killed many waterfowl as a result of oiled feathers and the intake of oil and more indirect physiological effects have been shown experimentally. Pollutants may affect waterfowl indirectly by changing the habitat and directly as a result of intake of toxic substances. They are unlikely to have been directly limiting factors in populations of such species as mallards. Their involvement with problem of other species, including canvasbacks (Aythya valisineria) and mergansers has still to be explored.

International Waterfowl Symposium↗
USGS1996

Environmental Contaminants in Wildlife: Interpreting Tissue Concentrations

Covers the complex issue of how to evaluate contaminants in wildlife. This comprehensive resource deals with the question: 'How much of a chemical in the tissues of an animal is harmful?' Features: Authoritative and sound advice is provided on many environmental contaminants, including what the contaminants are and how to interpret the data on them. Each chapter includes a review of the literature on a specific chemical, followed by a clear technical summary that provides research guidance. Direction is given on how to interpret data that are sometimes conflicting or insufficient. Data are presented in easy to use tables. Primary attention is given to toxic concentrations of contaminants such as organochlorine pesticides, PCBs, dioxins, PAHs, metals, and fluorides.

SETAC Special Publications Series.↗
USGS2023

Hydrologic framework and characterization of the Little Colorado River alluvial aquifer near Leupp, Arizona

The Little Colorado River alluvial aquifer near Leupp, Arizona, was investigated as a possible source of irrigation water for the Leupp and Birdsprings Chapters of the Navajo Nation. The physical, chemical, and hydraulic characteristics of the alluvial aquifer were studied using geophysical surveys, installation of observation wells, water-level measurements, chemical analyses, groundwater pumping simulations, and review of previous investigations. Geophysical surveys and well borings revealed that the aquifer ranges in thickness from near 0 feet around its periphery to about 100 feet in its thickest parts. Water levels were monitored in nine alluvial wells within the study area and compared with earlier measurements collected in 1998 and 1999. Comparison of those earlier water levels with water levels collected as part of this study showed a decline of between about 5 and 12 feet has occurred in the last 23 years. The water chemistry of the aquifer was analyzed for salinity hazard, sodium-adsorption hazard, and specific-ion toxicity. The sodium-adsorption hazard and specific-ion toxicity of alluvial aquifer water were found to be low. However, the salinity hazard was high enough in most areas that it could negatively affect salt-sensitive crops. Well-field pumping scenarios conducted for this study demonstrated that using groundwater from the alluvial aquifer for irrigated agriculture is theoretically possible but may be economically challenging owing to the hydraulic properties of the aquifer.

Arizona↗
USGS2003

Atomic weights of the elements. Review 2000 (IUPAC Technical Report)

A consistent set of internationally accepted atomic weights has long been an essential aim of the scientific community because of the relevance of these values to science and technology, as well as to trade and commerce subject to ethical, legal, and international standards. The standard atomic weights of the elements are regularly evaluated, recommended, and published in updated tables by the Commission on Atomic Weights and Isotopic Abundances (CAWIA) of the International Union of Pure and Applied Chemistry (IUPAC). These values are invariably associated with carefully evaluated uncertainties. Atomic weights were originally determined by mass ratio measurements coupled with an understanding of chemical stoichiometry, but are now based almost exclusively on knowledge of the isotopic composition (derived from isotope-abundance ratio measurements) and the atomic masses of the isotopes of the elements. Atomic weights and atomic masses are now scaled to a numerical value of exactly 12 for the mass of the carbon isotope of mass number 12. Technological advances in mass spectrometry and nuclear-reaction energies have enabled atomic masses to be determined with a relative uncertainty of better than 1 ×10−7 . Isotope abundances for an increasing number of elements can be measured to better than 1 ×10−3 . The excellent precision of such measurements led to the discovery that many elements, in different specimens, display significant variations in their isotope-abundance ratios, caused by a variety of natural and industrial physicochemical processes. While such variations increasingly place a constraint on the uncertainties with which some standard atomic weights can be stated, they provide numerous opportunities for investigating a range of important phenomena in physical, chemical, cosmological, biological, and industrial processes. This review reflects the current and increasing interest of science in the measured differences between source-specific and even sample-specific atomic weights. These relative comparisons can often be made with a smaller uncertainty than is achieved in the best calibrated “absolute ” (=SI-traceable) atomic-weight determinations. Accurate determinations of the atomic weights of certain elements also influence the values of fundamental constants such as the Avogadro, Faraday, and universal gas constants. This review is in two parts: the first summarizes the development of the science of atomic-weight determinations during the 20th century; the second summarizes the changes and variations that have been recognized in the values and uncertainties of atomic weights, on an element-by-element basis, in the latter part of the 20th century.

Pure and Applied Chemistry↗
USGS1915

Springs of California

In 1903 the United States Geological Survey began an investigation of the underground water of California, generally with financial cooperation on the part of the State. Since that year ten papers on the underground water of the State have been issued by the Survey, each representing an investigation that has been completed. The field work which is to serve as the basis for two additional papers has also been done and the reports are in preparation. Investigations have been begun in two other areas in the State and their results will eventually be assembled and published. Since a period soon after the inception of the California work those responsible for its conduct have realized the desirability of a special study of the springs, particularly those which yield mineral waters and which are utilized to a greater or less extent by citizens of the State and by tourists as recreation and health resorts. It did not become practicable to begin this work until the summer of 1908, when Mr. G. A. Waring, who had assisted in some of the earlier California studies and had investigated for the Survey certain areas in southern Oregon and Washington, was assigned to the task of collecting and assembling the necessary data. California, with an area of 158,000 square miles, is the second largest State in the Union. It exhibits wide geographic diversity, since it includes the lowest area in the United States Death Valley, 276 feet below sea level and the highest Mount Whitney, 14,501 feet above the sea; and accompanying this geographic diversity there is a corresponding range in scenic effects, climate, and vegetation. The records obtained at meteorological stations in the Salton Sink indicate a maximum temperature of 130° in the shade, the highest of record within the continental United States. It is probable that minimum temperatures on the higher peaks, like Mount Whitney and Mount Shasta, approach the minimum within our boundaries. Rainfall records in the most arid sections of the southern deserts of the State represent the extreme of aridity in the United States, with averages of less than 3 inches per annum and periods of 12 months or more with only traces of rain, whereas the precipitation in northwestern California is very heavy, an annual average of close to 100 inches being recorded at a few stations in Mendocino and Del Norte counties. The immensity of the area of the State has made the collection of the field data required for the report a task of considerable magnitude, though its diversity has added greatly to the interest of the work. In the original plan it was estimated that two years of field studies would prove sufficient. Mr. Waring succeeded in visiting the more important localities during this period, although some of his examinations were, of necessity, rather cursory. In midsummer, 1910, after the completion of the field work and the assembling of the greater portion of his data in manuscript form he was called by the Government of Brazil to take charge of general water supply investigations in the northeastern arid portion of that South American republic. The task of reviewing, editing, and supplementing in some respects, the results of his studies was thus unavoidably left to others. This task was rendered light by the systematic form in which Mr. Waring's material was left. It was a matter of regret to Mr. Waring, as it has been to those associated with him, that the financial limitations which controlled his work made it impracticable to procure the large number of new analyses which are particularly important in a paper of this type, in which waters of unusual chemical characteristics are discussed. Such analyses as are available have been assembled from all possible sources and combined with those which were prepared especially in connection with this investigation. The result, although it is in some respects unsatisfactory, furnishes a basis for a general view of the characteristics of the spring waters and serves to permit, their classification in a general way. Mr. Herman Stabler has reviewed the chemical data and rearranged and interpreted the available analyses. It is hoped that the report, setting forth as it does the results of impartial observations upon one of the important present and more important prospective resources of the State, will prove of value to its citizens as well as to its visitors, and that the assembled material will not be without interest to physicians, chemists, geologists, and teachers who may have especial need for the information contained in the volume.

California↗
USGS2022

Hyperspectral remote sensing of white mica: A review of imaging and point-based spectrometer studies for mineral resources, with spectrometer design considerations

Over the past ~30 years, hyperspectral remote sensing of chemical variations in white mica have proven to be useful for ore deposit studies in a range of deposit types. To better understand mineral deposits and to guide spectrometer design, this contribution reviews relevant papers from the fields of remote sensing, spectroscopy, and geology that have utilized spectral changes caused by chemical variation in white micas. This contribution reviews spectral studies conducted at the following types of mineral deposits: base metal sulfide, epithermal, porphyry, sedimentary rock hosted gold deposits, orogenic gold, iron oxide copper gold, and unconformity-related uranium. The structure, chemical composition, and spectral features of white micas, in this contribution defined as muscovite, paragonite, celadonite, phengite, illite, and sericite, are given. Reviewed laboratory spectral studies determined that shifts in the position of the white mica 2200 nm combination feature of 1 nm correspond to a change in Al oct content of approximately ±1.05%. Many of the reviewed spectral studies indicated that a shift in the position of the white mica 2200 nm combination feature of 1 nm was geologically significant. A sensitivity analysis of spectrometer characteristics; bandpass, sampling interval, and channel position, is conducted using spectra of 19 white micas with deep absorption features to determine minimum characteristics required to accurately measure a shift in the position of the white mica 2200 nm combination feature. It was determined that a sampling interval < 16.3 nm and bandpass <17.5 nm are needed to achieve a root mean square error (RMSE) of 2 nm, whereas a sampling interval < 8.8 nm and bandpass <9.8 nm are needed to achieve a RMSE of 1 nm. For comparison, commonly used imaging spectrometers HyMap, AVIRIS-Classic, SpecTIR®'s AisaFENIX 1K, and HySpex tm SWIR 384 have 2.1, 1.2, 0.96, and 0.95 nm RMSE in determining the position of the 2200 nm white mica combination feature, respectively. An additional sensitivity analysis is conducted to determine the effect of signal to noise ratio (SNR) on the RMSE of the position of the white mica 2200 nm combination feature, using spectra of 18 white micas with deep absorption features. For a spectrometer with sampling interval and bandpass of 1 nm, we estimate that RMSEs of 1 and 1.5 nm are achievable with spectra having a minimum SNR of approximately 246 and 64, respectively. For a spectrometer with sampling interval and bandpass of 5 nm, we estimate that RMSEs of 1 and 1.5 nm are attainable with spectra having a minimum SNR of approximately 431 and 84, respectively. When using a spectrometer with a sampling interval 8.8 nm and a bandpass of 9.8 nm, a RMSE of 1 is only achievable with convolved, noiseless reference spectra. For the 8.8_9.8 nm spectrometer, spectra with SNR of 250 and 100 result in RMSE of 1.1 and 1.3, respectively. Therefore, fine spectral resolution characteristics achieve RMSEs better than 1 nm for high SNR spectra while spectrometers with coarse spectral resolution have larger RMSE, perform well with noisy data, and are useful for white mica studies if RMSE of 1.1 to 1.5 nm is acceptable.

Remote Sensing of Environment↗
USGS1990

Chlordane Hazards to Fish, Wildlife, and Invertebrates: A Synoptic Review

Technical chlordane is an organochlorine compound first introduced into the United States in 1947 in a variety of formulations for use as a broad-spectrum pesticide. By 1974, about 9.5 million kilograms of chlordane were produced annually. Concern over the potential carcinogenicity of chlordane has led to sharply curtailed production. Since 1983, chlordane use in the United States has been prohibited, except for control of underground termites. Chlordane is readily absorbed by warmblooded animals through skin, diet, and inhalation, and distributed throughout the body. In general, residues of chlordane and its metabolites are not measurable in tissues 4 to 8 weeks after exposure, although metabolism rates varied significantly between species. Food chain biomagnification is usually low, except in some marine mammals. In most mammals, the metabolite oxychlordane has proven much more toxic and persistent than the parent chemical.

Contaminant Hazard Reviews↗
USGS1955

Is Carbon dioxide an ore-forming fluid under shallow-earth conditions?

A review of some of the physical-chemical properties of CO 2 and of the system CO 2 --H 2 O indicates that under some shallow-earth conditions CO 2 can exist as a separate phase with a density approximately that of water. The effect of dissolved neutral or acid salts on the solubility of CO 2 in H 2 O is not large. Carbonates, oxides, and silicates, through reactions with a CO 2 -saturated water phase, will eventually cause the disappearance of a CO 2 phase. The prevalence of CO 2 in the earth's crust is attested by its abundance in natural gases and fluid inclusions in minerals. Some of the characteristics of uranium ores of the Colorado Plateau are not incompatible with the assumption that deposition was from a fluid CO 2 phase.

Economic Geology↗
USGS1979

Organochlorine poisoning of herons

Over a period of years interested individuals have submitted many dead or moribund herons of various species to our laboratory to learn whether the birds had been affected by diseases or organochlorine poisoning. Residue concentrations in carcasses of birds and mammals are considered the best measure of sublethal exposure, whereas residues in brains are best to use for diagnosing death by most organochlorine chemicals (see Heinz et al. 1979 for review). Residue concentrations in brains that are diagnostic of organochlorine poisoning for birds have been determined in the laboratory for DDT and its metabolites (L.F. Stickel et al. 1966; W.H. Stickel et al. 1970; Stickel and Stickel 1970; W.H. Stickel, pers. comm.); dieldrin (W.H. Stickel et al. 1969; W.H. Stickel, pers. comm.); heptachlor, chlordane, and oxychlordane (L.F. Stickel et al. 1979; W.H. Stickel, pers. comm.); endrin (W.H. Stickel et al. 1979); Aroclor 1254 (W.H. Stickel 1975; W.H. Stickel, pers. comm.); and mirex (W.H. Stickel et al. 1973). This subject is discussed in further detail by Heinz et al. (1979). The purpose of the present paper is to document the occurrence and concentration of organochlorine residues in the brains of herons from various areas in the United States. By comparing these residue concentrations with laboratory-determined diagnostic lethal levels, we conclude that some herons were killed by organochlorine poisoning; others were at least seriously endangered by the residues they carried. Complete results of carcass analyses for these and other herons, as well as further details on residues in brains, will be reported elsewhere (H.M. Ohlendorf, D.M. Swineford, and L.N. Locke, unpublished manuscript). Overall, we analyzed carcasses or brains of more than 70 herons found dead or moribund and 36 others taken in planned collections. Residue levels in carcasses of many herons were not high enough to warrant analysis of brains. In the present paper we compare carcass and brain residues of dieldrin in 23 herons of which both carcass and brain were analyzed.

Alabama, Michigan, Vermont↗
USGS1997

The effects of pollutants on wildlife

In this chapter, selected sources of information which address the effects of pollutants on wildlife are reviewed. Although naturally occurring plant and animal toxins also affect wildlife, the focus of this review is xenobiotic toxicants. Xenobiotic substances are chemicals introduced into the environment in the form of pesticides, heavy metals, polychlorinated biphenyls (PCBs), and other by-products of human activities. The science of examining the effects of these substances on animal and plant life is multi-disciplinary in nature and contributors to the literature in this field include toxicologists, wildlife and aquatic ecologists, chemists and those in the veterinary and medical professions.

Book chapter↗
USGS1988

Agricultural chemicals and the quality of prairie-pothole wetlands for adult and juvenile waterfowl - What are the concerns?

A review of the literature and results of ongoing studies indicates that the potential for agricultural chemicals, particularly aerially-applied insecticides, to enter prairie potholes and reduce the quality of these wetlands for waterfowl is great, and that a coordinated effort by farmers, wildlife managers, and regulatory agencies is needed to minimize these impacts

Biological Report↗
USGS2011

Advancing environmental toxicology through chemical dosimetry: External exposures versus tissue residues

The tissue residue dose concept has been used, although in a limited manner, in environmental toxicology for more than 100 y. This review outlines the history of this approach and the technical background for organic chemicals and metals. Although the toxicity of both can be explained in tissue residue terms, the relationship between external exposure concentration, body and/or tissues dose surrogates, and the effective internal dose at the sites of toxic action tends to be more complex for metals. Various issues and current limitations related to research and regulatory applications are also examined. It is clear that the tissue residue approach (TRA) should be an integral component in future efforts to enhance the generation, understanding, and utility of toxicity testing data, both in the laboratory and in the field. To accomplish these goals, several key areas need to be addressed: 1) development of a risk-based interpretive framework linking toxicology and ecology at multiple levels of biological organization and incorporating organism-based dose metrics; 2) a broadly applicable, generally accepted classification scheme for modes/mechanisms of toxic action with explicit consideration of residue information to improve both single chemical and mixture toxicity data interpretation and regulatory risk assessment; 3) toxicity testing protocols updated to ensure collection of adequate residue information, along with toxicokinetics and toxicodynamics information, based on explicitly defined toxicological models accompanied by toxicological model validation; 4) continued development of residueeffect databases is needed ensure their ongoing utility; and 5) regulatory guidance incorporating residue-based testing and interpretation approaches, essential in various jurisdictions. ??:2010 SETAC.

Integrated Environmental Assessment and Management↗
USGS2023

Geology, hydrology, and groundwater contamination in the vicinity of Central Chemical facility, Hagerstown, Maryland

The soil and groundwater at the Central Chemical facility, Hagerstown, Maryland, are contaminated due to the blending and production of pesticides and fertilizers during much of the 20th century. Remedial investigations focus on two operable units (OU) consisting of the surface soils and waste disposal lagoon (OU-1) and the groundwater (OU-2). The contaminants of concern (COC) for groundwater include 41 compounds categorized within the subgroups of volatile organic compounds (VOCs), semi-volatile organic compounds (SVOCs), pesticides, and metals. The purpose of this report is to provide a conceptual site model of the hydrogeology and groundwater contaminant transport at and near the Central Chemical facility. The conceptual model was developed through review, synthesis, and interpretation of the results of hydrogeologic, soil, and other environmental investigations conducted at and in the vicinity of the facility in recent decades and is intended to support plans for environmental remediation of the groundwater in OU-2. The extent and nature of the groundwater contaminant plume associated with the bedrock was characterized for OU-2 of the site. Lithologic and structural comparisons between shallow soil, weathered rock, and epikarst and deeper competent but bedded, dipping, fractured, and karstic limestones illustrate two connected flow systems—a surficial flow system consisting of the unconsolidated overburden and epikarst and a structurally dominant bedrock flow system below the epikarst. Uncertainties exist regarding the nature and transport of contaminants within the epikarst system particularly within voids and perched epikarst water tables. Karst dissolution features are observed within the site including sinkholes and dissolution voids within wells at the site. Of interest, one well in the northern part of the study area (MW-J-71) appears to have a dissolution void connected to an offsite well (OW-2-115) farther to the north. This connection is supported by groundwater level data and elevated concentrations of total suspended solids (TSS) and chlorobenzene in both wells. The high level of TSS supports the possibility of offsite transport of particle-bound contaminants within the conduit system. Episodically elevated concentrations of COC from different groups also were observed within select wells in the epikarst near the waste disposal lagoon (particularly MW-A-51). The variability observed between different COC within the same well may be the result of additional contaminated source materials unrelated to the disposal lagoon. Storage and episodic transport of contaminated material within the epikarst system has the potential to hinder remediation efforts if not considered in the remedial action.

Maryland↗
USGS1953

Relationship between chemical structure and rat repellency

Repellent activity is defined as the activity of a compound in preventing consumption of, or gnawing attacks upon, foodstuffs or articles containing or treated with the candidate substance. Data are presented on repellency indices of 2700 compounds, and it is shown that repellency is associated with specific functional groups attached to alkyl, aryl, or heterocyclic nuclei. Functional groups containing nitrogen, sulfur or halogens are most active, with amines, imides, thiocyanates and thiocarbamates forming some of the most active classes. Activity of any functional group may be affected by molecular weight, unsaturation, or spatial configuration of the nucleus, or by the presence of additional substituent groups.

National Research Council, Chemical-Biological Coo↗
USGS2024

EthoCRED: A framework to guide reporting and evaluation of the relevance and reliability of behavioural ecotoxicity studies

Behavioural analysis has been attracting significant attention as a broad indicator of sub-lethal toxicity and has secured a place as an important subdiscipline in ecotoxicology. Among the most notable characteristics of behavioural research, compared to other established approaches in sub-lethal ecotoxicology (e.g. reproductive and developmental bioassays), are the wide range of study designs being used and the diversity of endpoints considered. At the same time, environmental hazard and risk assessment, which underpins regulatory decisions to protect the environment from potentially harmful chemicals, often recommends that ecotoxicological data be produced following accepted and validated test guidelines. These guidelines typically do not address behavioural changes, meaning that these, often sensitive, effects are not represented in hazard and risk assessments. Here, we propose a new tool, the EthoCRED evaluation method, for assessing the relevance and reliability of behavioural ecotoxicity data, which considers the unique requirements and challenges encountered in this field. This method and accompanying reporting recommendations are designed to serve as an extension of the “Criteria for Reporting and Evaluating Ecotoxicity Data (CRED)” project. As such, EthoCRED can both accommodate the wide array of experimental design approaches seen in behavioural ecotoxicology, and could be readily implemented into regulatory frameworks as deemed appropriate by policy makers of different jurisdictions to allow better integration of knowledge gained from behavioural testing into environmental protection. Furthermore, through our reporting recommendations, we aim to improve the reporting of behavioural studies in the peer-reviewed literature, and thereby increase their usefulness to inform chemical regulation.

Biological Reviews↗