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Maps showing distribution of iron, cobalt, barium, strontium, arsenic, antimony, and bismuth in samples of minus-60-mesh (0.25-MM) stream sediment and (or) nonmagnetic heavy-mineral concentrate, Walker Lake 1 degree by 2 degrees Quadrangle, California and Nevada

This report is part of a folio of maps of the Walker Lake 1 o x 2 o quadrangle, California and Nevada, prepared under the Conterminous United States Mineral Assessment Program. The folio includes geological, geochemical, and geophysical maps, as well as mineral resources assessment maps, which identify selected known or possible mineral-deposit environments in the quadrangle. The geochemical maps show the distributions of selected individual elements (Chaffee and others, 1988 a, b, c) and the distributions of selected groups of elements (Chaffee, 1988a, b, c). Discussions accompanying the individual element maps are restricted to mineral residences of the individual elements as well as to what types of mineral deposits and environments may be represented by anomalies of a particular element. Discussions accompanying the multielemental maps describe the types of mineral deposits that may be related to each element group and indicate the most favorable localities for these deposits.

California, Nevada

Maps showing distribution of anomalies based on the use of R-mode factor analysis for selected groupings of elements in samples of minus-60-mesh (0.25-MM) stream sediment and nonmagnetic heavy-mineral concentrate, Walker Lake 1 degree by 2 degrees Quadrangle, California and Nevada

This report is part of a folio of maps of the Walker Lake 1 o x 2 o quadrangle, California and Nevada, prepared under the Conterminous United States Mineral Assessment Program. The folio includes geological, geochemical, and geophysical maps, as well as mineral resources assessment maps, which identify selected known or possible mineral-deposit environments in the quadrangle. The geochemical maps show the distributions of selected individual elements (Chaffee and others, 1988 a, b, c) and the distributions of selected groups of elements (Chaffee, 1988a, b, c). Discussions accompanying the individual element maps are restricted to mineral residences of the individual elements as well as to what types of mineral deposits and environments may be represented by anomalies of a particular element. Discussions accompanying the multielemental maps describe the types of mineral deposits that may be related to each element group and indicate the most favorable localities for these deposits.

California, Nevada

Maps showing distribution of anomalies based on the use of scoresum plots for selected groupings of elements in samples of minus-60-mesh (0.25-MM) stream sediment, Walker Lake 1 degree by 2 degrees Quadrangle, California and Nevada

This report is part of a folio of maps of the Walker Lake 1 o x 2 o quadrangle, California and Nevada, prepared under the Conterminous United States Mineral Assessment Program. The folio includes geological, geochemical, and geophysical maps, as well as mineral resources assessment maps, which identify selected known or possible mineral-deposit environments in the quadrangle. The geochemical maps show the distributions of selected individual elements (Chaffee and others, 1988 a, b, c) and the distributions of selected groups of elements (Chaffee, 1988a, b, c). Discussions accompanying the individual element maps are restricted to mineral residences of the individual elements as well as to what types of mineral deposits and environments may be represented by anomalies of a particular element. Discussions accompanying the multielemental maps describe the types of mineral deposits that may be related to each element group and indicate the most favorable localities for these deposits.

California, Nevada

Maps showing distribution of anomalies based on the use of scoresum plots for selected groupings of elements in samples of nonmagnetic heavy-mineral concentrate, Walker Lake 1 degree by 2 degrees Quadrangle, California and Nevada

This report is part of a folio of maps of the Walker Lake 1 o x 2 o quadrangle, California and Nevada, prepared under the Conterminous United States Mineral Assessment Program. The folio includes geological, geochemical, and geophysical maps, as well as mineral resource assessment maps which identify selected known or possible mineral-deposit environments in the quadrangle. The geochemical maps show the distributioins of selected individual elements (Chaffee and others 1988a, b, c, d) and the distributions of selected groups of elements (Chaffee, 1988a, b). Discussions accompanying the individual element maps are restricted to possible mineral residences of the individual elements as well as to what types of mineral deposits and environments may be represented by anomalies of a particular element. Discussions accompanying the multielement maps describe the types of mineral deposits that may be related to each element group and indicate the most favorable localities for these deposits.

California, Nevada

Western Mineral and Environmental Resources Science Center--providing comprehensive earth science for complex societal issues

Minerals in the environment and products manufactured from mineral materials are all around us and we use and come into contact with them every day. They impact our way of life and the health of all that lives. Minerals are critical to the Nation's economy and knowing where future mineral resources will come from is important for sustaining the Nation's economy and national security. The U.S. Geological Survey (USGS) Mineral Resources Program (MRP) provides scientific information for objective resource assessments and unbiased research results on mineral resource potential, production and consumption statistics, as well as environmental consequences of mining. The MRP conducts this research to provide information needed for land planners and decisionmakers about where mineral commodities are known and suspected in the earth's crust and about the environmental consequences of extracting those commodities. As part of the MRP scientists of the Western Mineral and Environmental Resources Science Center (WMERSC or 'Center' herein) coordinate the development of national, geologic, geochemical, geophysical, and mineral-resource databases and the migration of existing databases to standard models and formats that are available to both internal and external users. The unique expertise developed by Center scientists over many decades in response to mineral-resource-related issues is now in great demand to support applications such as public health research and remediation of environmental hazards that result from mining and mining-related activities. Western Mineral and Environmental Resources Science Center Results of WMERSC research provide timely and unbiased analyses of minerals and inorganic materials to (1) improve stewardship of public lands and resources; (2) support national and international economic and security policies; (3) sustain prosperity and improve our quality of life; and (4) protect and improve public health, safety, and environmental quality. The MRP supports approximately 40 USGS research specialists who utilize cooperative agreements with universities, industry, and other governmental agencies to support their collaborative research and information exchange. Scientists of the WMERSC study how and where non-fuel mineral resources form and are concentrated in the earth's crust, where mineral resources might be found in the future, and how mineral materials interact with the environment to affect human and ecosystem health. Natural systems (ecosystems) are complex - our understanding of how ecosystems operate requires collecting and synthesizing large amounts of geologic, geochemical, biologic, hydrologic, and meteorological information. Scientists in the Center strive to understand the interplay of various processes and how they affect the structure, composition, and health of ecosystems. Such understanding, which is then summarized in publicly available reports, is used to address and solve a wide variety of issues that are important to society and the economy. WMERSC scientists have extensive national and international experience in these scientific specialties and capabilities - they have collaborated with many Federal, State, and local agencies; with various private sector organizations; as well as with foreign countries and organizations. Nearly every scientific and societal challenge requires a different combination of scientific skills and capabilities. With their breadth of scientific specialties and capabilities, the scientists of the WMERSC can provide scientifically sound approaches to a wide range of societal challenges and issues. The following sections describe examples of important issues that have been addressed by scientists in the Center, the methods employed, and the relevant conclusions. New directions are inevitable as societal needs change over time. Scientists of the WMERSC have a diverse set of skills and capabilities and are proficient in the collection and integration of

Circular

Development of industrial minerals in Colorado

Technology and engineering have helped make mining safer and cleaner for both humans and the environment. Inevitably, mineral development entails costs as well as benefits. Developing a mine is an environmental, engineering, and planning challenge that must conform to many Federal, State, and local regulations. Community collaboration, creative design, and best management practices of sustainability and biodiversity can be positive indicators for the mining industry. A better understanding of aesthetics, culture, economics, geology, climate, vegetation and wildlife, topography, historical significance, and regional land planning is important in resolving land-use issues and managing mineral resources wisely. Ultimately, the consuming public makes choices about product use (including water, food, highways, housing, and thousands of other items) that influence operations of the mineral industry. Land planners, resource managers, earth scientists, designers, and public groups have a responsibility to consider sound scientific information, society's needs, and community appeals in making smart decisions concerning resource use and how complex landscapes should change. An effort to provide comprehensive geosciences data for land management agencies in central Colorado was undertaken in 2003 by scientists of the U.S. Geological Survey and the Colorado Geological Survey. This effort, the Central Colorado Assessment Project, addressed a variety of land-use issues: an understanding of the availability of industrial and metallic rocks and minerals, the geochemical and environmental effects of historic mining activity on surface water and groundwater, and the geologic controls on the availability and quality of groundwater. The USDA Forest Service and other land management agencies have the opportunity to contribute to the sustainable management of natural aggregate and other mineral resources through the identification and selective development of mineral resources and the reclamation of mines on lands that they administer. The information in this Circular will help them carry out that task.

Colorado

Silt fraction heavy-mineral distributions in a lateritic environment: The rivers and insular shelf of north-central Puerto Rico

This fraction, which is enriched in heavy minerals relative to the sand fraction, is mainly detrital but contains a strong authigenic component. The authigenic silt heavy-mineral fraction is largely a product of the lateritic weathering and dominated by iron oxides and alterites. Grains of bladed rutile and leached ilmenite are common. Spatial variability in silt-fraction mineralogy is considerable. Within the Rio Cibuco system variability is related to compositional differences in rapidly eroding source rocks. On the shelf, silt heavy-mineral abundances are greatest at the river mouths and decrease seaward. Variability in the shelf samples is controlled primarily by source rivers and shelf sorting processes.

Puerto Rico

Heavy-mineral provenance in an estuarine environment, Willapa Bay, Washington, USA: palaeogeographic implications and estuarine evolution

Modern sediments from representative localities in Willapa Bay, Washington, comprise two principal heavy-mineral suites. One contains approximately equivalent amounts of hornblende, orthopyroxene, and clinopyroxene; this is derived from the Columbia River, which discharges into the Pacific Ocean a short distance south of the bay. The other suite, dominated by clinopyroxene, is restricted to sands of rivers flowing into the bay from the east. The heavy-mineral distributions within the bay suggest that sand discharged from the Columbia River, borne north by longshore transport and carried into the bay by tidal currents, accounts for nearly all of the sand within the interior of Willapa Bay today. Pleistocene deposits on the east side of the bay contain three heavy-mineral assemblages, two of which are identical to the modern assemblages described above. These assemblages reflect the relative influence of tidal and fluvial processes on the Late Pleistocene deposits (100,000–200,000 BP. Amino acid racemization in Quaternary shell deposits at Willapa Bay, Washington. Geochimica et Cosmochimica Acta 43, 1505–1520). They are also consistent with those processes inferred on the basis of sedimentary structures and stratigraphic relations in about two-thirds of the samples examined. Anomalies can be explained by recycling of sand from older deposits. The persistence of the two heavy-mineral suites suggests that the pattern of estuarine sedimentation in Late Pleistocene deposits closely resembled that of the modern bay. The third heavy-mineral suite is enriched in epidote and occurs in a few older Pleistocene units. On the north side of the bay, the association of this suite with southwest-directed foresets in cross-bedded gravel indicates derivation from the northeast, perhaps from an area of glacial outwash. The presence of this suite in ancient estuarine sands exposed on the northeast side of the bay suggests that input from this northerly source may have intermittently dominated Willapa Bay deposition in the past.

Washington

Depositional environments as a guide to uranium mineralization in the Chinle Formation, San Rafael Swell, Utah

Uranium deposits in the San Rafael Swell are related to sedimentary depositional environments in the Upper Triassic Chinle Formation. The sedimentary textures resulting from depositional processes operating in low-energy environments appear to have influenced uranium mineralization. The Ohinle consists of three fining-upward, fluvial-lacustrine sequences. Uranium minerals are concentrated in the lower part of the lowest sequence in areas where sediments of low-energy environments are complexly interbedded with sediments of other environments. Areas favorable for uranium exploration exist in the subsurface to the north, west, and south of the Chinle outcrop in the Swell. This determination is based on the spatial distribution of depositional environments and the pattern of Chinle deposition through time.

Utah

Scoresum - A technique for displaying and evaluating multi-element geochemical information, with examples of its use in regional mineral assessment programs

A technique called SCORESUM was developed to display a maximum of multi-element geochemical information on a minimum number of maps for mineral assessment purposes. The technique can be done manually for a small analytical data set or can be done with a computer for a large data set. SCORESUM can be used with highly censored data and can also weight samples so as to minimize the chemical differences of diverse lithologies in different parts of a given study area. The full range of reported analyses for each element of interest in a data set is divided into four categories. Anomaly scores — values of O (background), 1 (weakly anomalous), 2 (moderately anomalous), and 3 (strongly anomalous) — are substituted for all of the analyses falling into each of the four categories. A group of elements based on known or suspected association in altered or mineralized areas is selected for study and the anomaly scores for these elements are summed for each sample site and then plotted on a map. Some of the results of geochemical studies conducted for mineral assessments in two areas are briefly described. The first area, the Mokelumne Wilderness and vicinity, is a relatively small and geologically simple one. The second, the Walker Lake 1° × 2° quadrangle, is a large area that has extremely complex geology and that contains a number of different mineral deposit environments. These two studies provide examples of how the SCORESUM technique has been used (1) to enhance relatively small but anomalous areas and (2) to delineate and rank areas containing geochemical signatures for specific suites of elements related to certain types of alteration or mineralization.

Journal of Geochemical Exploration

Sediment-hosted gold deposits of the world: Database and grade and tonnage models

All sediment-hosted gold deposits (as a single population) share one characteristic—they all have disseminated micron-sized invisible gold in sedimentary rocks. Sediment-hosted gold deposits are recognized in the Great Basin province of the western United States and in China along with a few recognized deposits in Indonesia, Iran, and Malaysia. Three new grade and tonnage models for sediment-hosted gold deposits are presented in this paper: (1) a general sediment-hosted gold type model, (2) a Carlin subtype model, and (3) a Chinese subtype model. These models are based on grade and tonnage data from a database compilation of 118 sediment-hosted gold deposits including a total of 123 global deposits. The new general grade and tonnage model for sediment-hosted gold deposits (n=118) has a median tonnage of 5.7 million metric tonnes (Mt) and a gold grade of 2.9 grams per tonne (g/t). This new grade and tonnage model is remarkable in that the estimated parameters of the resulting grade and tonnage distributions are comparable to the previous model of Mosier and others (1992). A notable change is in the reporting of silver in more than 10 percent of deposits; moreover, the previous model had not considered deposits in China. From this general grade and tonnage model, two significantly different subtypes of sediment-hosted gold deposits are differentiated: Carlin and Chinese. The Carlin subtype includes 88 deposits in the western United States, Indonesia, Iran, and Malaysia, with median tonnage and grade of 7.1 Mt and 2.0 g/t Au, respectively. The silver grade is 0.78 g/t Ag for the 10th percentile of deposits. The Chinese subtype represents 30 deposits in China, with a median tonnage of 3.9 Mt and medium grade of 4.6 g/t Au. Important differences are recognized in the mineralogy and alteration of the two sediment-hosted gold subtypes such as: increased sulfide minerals in the Chinese subtype and decalcification alteration dominant in the Carlin type. We therefore recommend using the appropriate grade and tonnage model presented in this study for mineral resource assessments depending on the geologic and mineralogical data available for a region. Tonnage and contained gold within the general sediment-hosted gold model are analyzed based on major geologic features such as tectonic setting and magmatic (dikes, sills, and stocks) or amagmatic environment. The results show a significant difference in tonnage and contained gold, with higher median values in deposits spatially associated with igneous rocks, regardless of structural style of the deposit. These results suggest that magmatic environments control mineralization intensity—an important consideration in the regional assessment of prospective areas for sediment-hosted gold deposits.

Open-File Report

Geochemistry and jasper beds from the Ordovician Løkken ophiolite, Norway: origin of proximal and distal siliceous exhalites

Stratiform beds of jasper (hematitic chert), composed essentially of SiO 2 (69–95 wt %) and Fe 2 O 3 (3–25 wt %), can be traced several kilometers along strike in the Ordovician Løkken ophiolite, Norway. These siliceous beds are closely associated with volcanogenic massive sulfide (VMS) deposits and are interpreted as sea-floor gels that were deposited by fallout from hydrothermal plumes in silica-rich seawater, in which plume-derived Fe oxyhydroxide particles promoted flocculation and rapid settling of large (~200 μm) colloidal particles of silica-iron oxyhydroxide. Concentrations of chalcophile elements in the jasper beds are at the parts per million level implying that sulfide particle fallout was insignificant and that the Si-Fe gel-forming plumes were mainly derived from intermediate- (100°–250°C) to high-temperature (>250°C) white smoker-type vents with high Fe/S ratios. The interpreted setting is similar to that of the Lau basin, where high-temperature (280°–334°C) white smoker venting alternates or overlaps with sulfide mound-forming black smoker venting. Ratios of Al, Sc, Th, Hf, and REE to iron are very low and show that the detrital input was <0.1 percent of the bulk jasper. Most jasper beds are enriched in U, V, P, and Mo relative to the North American Shale Composite, reflecting a predominantly seawater source, whereas REE distribution patterns (positive Eu and negative Ce anomalies) reflect variable mixing of hydrothermal solutions with oxic seawater at dilution ratios of ~10 2 to 10 4 . Trace element variations in the gel precursor to the jasper are thought to have been controlled by coprecipitation and/or adsorption by Fe oxyhydroxide particles that formed by the oxidation of hydrothermal Fe 2+ within the variably seawater-diluted hydrothermal plume(s). Thick jasper layers near the Høydal VMS orebody show distinct positive As/Fe and Sb/Fe anomalies that are attributed to near-vent rapid settling of Si-Fe particles derived from As- and Sb-rich hydrothermal fluids prior to extensive mixing with seawater in the buoyant plume. Particles that formed later in the highly diluted nonbuoyant plume formed relatively As and Sb poor distal jasper. The large particle sizes and accordingly high settling rates of the particles, together with mass-balance calculations based on modern vent field data, suggest that individual meter-thick jasper beds formed within a plume lifetime of 200 years or less. The lack of thick jasper beds near the Løkken VMS orebody, which is larger than the Høydal orebody by more than two orders of magnitude, probably reflects a shift to anoxic conditions during Løkken mineralization. This environment limited oxidation of iron in the hydrothermal plume and formation of the ferric oxyhydroxides necessary for the flocculation of silica and sea-floor deposition of the gel precursor of the jasper beds. Distal pyritic and iron-poor cherts are more common than jasper in ancient VMS-hosting sequences. The origin of these other types of siliceous exhalite is enigmatic but at least in some cases involved sulfidation, reduction to magnetite, or dissolution of the original ferric iron in precursor Si-rich gels, either by hydrothermal or diagenetic processes.

Economic Geology

Ground- and surface-water chemistry of Handcart Gulch, Park County, Colorado, 2003-2006

As part of a multidisciplinary project to determine the processes that control ground-water chemistry and flow in mineralized alpine environments, ground- and surface-water samples from Handcart Gulch, Colorado were collected for analysis of inorganic solutes and water and dissolved sulfate stable isotopes in selected samples. The primary aim of this study was to document variations in ground-water chemistry in Handcart Gulch and to identify changes in water chemistry along the receiving stream of Handcart Gulch. Water analyses are reported for ground-water samples collected from 12 wells in Handcart Gulch, Colorado. Samples were collected between August 2003 and October 2005. Water analyses for surface-water samples are reported for 50 samples collected from Handcart Gulch and its inflows during a low-flow tracer injection on August 6, 2003. In addition, water analyses are reported for three other Handcart Gulch stream samples collected in September 2005 and March 2006. Reported analyses include field parameters (pH, specific conductance, temperature, dissolved oxygen, and Eh), major and trace constituents, oxygen and hydrogen isotopic composition of water and oxygen and sulfur isotopic composition of dissolved sulfate. Ground-water samples from this study are Ca-SO4 type and range in pH from 2.5 to 6.8. Most of the samples (75 percent) have pH values between 3.3 and 4.3. Surface water samples are also Ca-SO4 type and have a narrower range in pH (2.7?4.0). Ground- and surface-water samples vary from relatively dilute (specific conductance of 68 ?S/cm) to concentrated (specific conductance of 2,000 ?S/cm).

Colorado

Relation of uranium to hypogene mineral zoning in the Front Range mineral belt, Colorado

Many of the mining districts of the Colorado Front Range mineral belt contain mesothermal sulfide ores that exhibit a zonal distribution. Present data indicate that in most of the zoned districts pitchblende and/or secondary uranium minerals are most abundant in a transition zone between central areas containing predominantly pyritic gold ores and peripheral areas containing dominantly lead-zinc-silver deposits. Copper in the form of chalcopyrite is also probably more abundant in the transition zone than in adjacent zones. Many mineralized areas in the Front Range mineral belt are roughly co-extensive with and probably related to groups of Tertiary intrusives. The solutions that deposited sulfide and pitchblende in these areas probably were derived from many different types of source magma, but some bostonite magmas were probably particularly important sources of uranium-bearing solutions. At most localities where the relative ages of pitchblende and associated sulfides are known, the pitchblende is early in the paragenetic sequence, and not of intermediate age as suggested by its zonal position. This discrepancy may be the result of overlapping zones of deposition related to adjacent centers of mineralization, to changing environments of deposition within zones during the period of mineralization, or to unknown factors. Uranium is also present in districts in which the dominant mineralization is markedly different from the common pyritic gold-base metal sulfide mineralization. In the Jamestown district uranium appears to be associated'.mainly with fluorspar;, in other districts that exhibit little or no systematic hypogene zoning) it is ubiquitous. If uranium is present in zoned districts, a large proportion of she deposits probably should be in the transition zones. The application of this concept may be a valuable guide in prospecting for uranium.

Arizona;Colorado

Geochemistry of sulfate minerals in high- and low-temperature environments: A tribute to Robert O. Rye

This special issue is a tribute to Robert O. Rye, known as "Bob" to most, in light of his highly productive and ongoing career. Almost all of the papers in this issue are derived from topical sessions on sulfate minerals in hydrothermal and low-temperature environments. The sessions, held at the 2000 Geological Society of America meeting in Reno, NV, and sponsored jointly by the Mineralogical Society of America, the Society of Economic Geologists and the Geochemical Society, included 29 oral and 9 poster presentations. The sessions complemented a short course on the crystallography, geochemistry and environmental significance of sulfate minerals, sponsored by the Mineralogical Society of America and the Geochemical Society, which immediately preceded the meeting (Alpers et al., 2000). The 23 papers in this special issue typify the breadth of Bob Rye’s research in this important area of geochemistry.

Chemical Geology

Ion exchange in clays and other minerals

Ion exchange in clays and other minerals is dependent on the crystalline structure of the mineral and on the chemical composition of any solution in contact with the mineral. The structures of clay minerals and zeolites are briefly described to provide a background for the discussion of their ion-exchange reactions. Ion exchange in these minerals is a reversible chemical reaction that takes place between ions held near a mineral surface by unbalanced electrical charges within the mineral framework and ions in a solution in contact with the mineral. Generally the excess charge on the mineral is negative, and it attracts cations from the solution to neutralize this charge. The chemical reactions in ion exchange follow the law of mass action, but the reactions are restricted by the number of exchange sites on the mineral and by the strength of the bonding of the exchangeable cations to the mineral surface. Titration of H-clays with bases shows that montmorillonites and "illites" behave like a mixture of two or three different acids, whereas kaolinite, with an indefinite number of exchange sites, behaves like an indefinite number of acids. Ion-exchange capacity is measured in chemical equivalents of base adsorbed at pH 7. Each clay mineral has a range of exchange capacities because of differences in structure and in chemical composition. The ranges (in milliequivalents per 100 grams) are kaolinite, 3-15; halloysite (2H 2 O), 5-10; halloysite (4H 2 O), 40-50; montmorillonite, 70-100; "illite," 10-40; vermiculite, 100-150; glauconite, 11-20; attapulgite, 20-30; and allophane, 70. The common metallic cations found in exchange positions in clay minerals are Ca +2 , Mg +2 , Na + , and K + . At low pH values H + replaces other cations. The order of replaceability of the common cations has been found to be: Li + < Na + < K + < Rb + < Cs + and Mg +2 < Ca+2 < Sr +2 < Ba +2 Bivalent cations enter the exchange sites preferentially to univalent cations. The common exchangeable cation in most clay minerals in soils is Ca +2 . Other exchange phenomena discussed are anion exchange, fixation of cations and anions by clay minerals, effect of environment on cation exchange, and the exchange capacity of zeolites, of rocks, of other minerals, of organic matter and organic complexes, and of amorphous mineral material.

GSA Bulletin

Water resources inventory of Connecticut Part 10: Lower Connecticut River basin

The lower Connecticut River basin study area in south-central Connecticut includes 639 square miles and is drained principally by the Connecticut River and by seven smaller streams that flow directly to Long Island Sound between the West River on the west and the Connecticut River on the east. The population in 1979 was estimated to be 210,380. Much of the industrial development and population centers are in the Mattabesset River basin in the northwestern part, and the largest water use is also in the Mattabesset River basin. Precipitation averages 47 inches per year and provides an abundant supply of water. About 20 inches returns to the atmosphere as evapotranspiration, and the remainder either flows directly to streams or percolates to the water table, eventually discharging to Long Island Sound. Small quantities of water are exported from the basin by the New Haven and Meridan Water Departments, and small quantities are imported by the New Britain Water Department and Metropolitan Direct Commission. Precipitation during 1931-60 resulted in an average annual runoff of 302 billion gallons. In inflow from the Connecticut River is added to the average annual runoff, the 4,370 billion gallon s per year is potentially available for water ue. The domestic, institutional, commercial, and industrial (other than cooling water) water use for 1970 was 7 billion gallons, which is only 3 percent of the total water used, whereas 97 percent of the total is cooling water for power plants. Approximately 60 percent of the 7 billion gallons is treated before being discharged back to the streams. The total amount of fresh water used during 1970 was estimated to be 256,000 million gallons (Mgal), of which 247,000 Mgal was used for cooling water at stream electric-generating plants. The quantity for domestic, commercial, industrial, and agricultural used was 9,000 Mgal, which was approximately 120 gallons a day per person. Public water systems providing 70 percent of these requirement and all the systems supplying water met the drinking water standards of the Connecticut General Assembly (1975). Till is widespread and generally provides only small amounts of water. Wells in till normally yield only a few hundred gallons of water daily and may be inadequate during dry periods. The thickness of of till ranges from 0 to 15 feet; a median thickness of 26 feet is estimated from information provided in drillers' logs of 467 wells penetrating underlying bedrock. The till is generally used only as an emergency or secondary source of water. Bedrock aquifers underlie the entire area and include sedimentary and crystalline (igneous and metamorphic) rock types. These aquifers supply small and usually reliable quantities of water to wells and are the chief source of water for many rural homes and farms., About 90 percent of the wells tapping bedrock yield at least 2 gal/min. The median yields from wells tapping aquifers in sedimentary, igneous, and metamorphic rocks are 11, 8, and 6.5 gal/min, respectively. The quantity of water potentially available from stratified drift was estimated on the basis of hydraulic characteristics of the aquifers, mathematical modeling of the aquifer system, and evaluation of natural and induced recharge. Long-term yields estimated or ten areas underlain by significant thickness of stratified drift range from 0.4 to 4.4 million gallons per day (Mgal/d). A change in well spacing or numbering could increase the long-term yields, but detailed modeling verification studies are needed to confirm optimal well locations. The chemical and physical (turbidity, color, taste, and sediment load) quality of water is good. The water if generally low in dissolved solids and is classified as soft to hard. Surface water is less mineralized than ground water, especially during high flow, when it is primarily derived from surface runoff rather than groundwater runoff. A median dissolved-solids concentration of 42 milligrams per liter (mg/L) and median hardness of 18 mg/L were determined from water samples collected from 26 streams during the high-flow period. During the low-flow period, median dissolved-solids concentration of 61 mg/L and median hardness of 27 mg/L were determined from sample from the same streams. The quality of water in stratified-drift and crystalline-rock aquifers is generally better than that in the sedimentary-rock aquifers. Water from 32 wells tapping stratified drift had median dissolved-solids concentrations of 116 mg/L; and 33 wells tapping stratified drift and 42 tapping crystalline rock had median hardness of 73 mg/L and 68 mg/L, respectively. Water from 32 wells tapping sedimentary rock had median dissolved concentrations of 231 and 156 mg/L, respectively. Sedimentary rock generally yields the hardest water. Iron and manganese occur objectionable concentrations in places, particularly in water from streams draining swamps and in water from aquifers either rich in iron and manganese-nearing minerals or where the reducing environment for solution of these minerals is favorable. Concentrations of iron in excess of 0.3 mg/L were found in 35 percent of the high streamflow samples, and in 45 percent of the ground-water samples. Most of the high iron and manganese concentration in streams and aquifers are found east of the Connecticut River. Human activities and tidal influence along the coast have modified the quality of water in much f the study area. The greatest influence from human activities has been in the northwestern part, in the Mattabesset River basin. There, the quality of water has been affected by domestic and animal wastes, which cause high dissolved-solids concentrations, high nitrate and phosphate loads and high bacterial counts. In the entire area, high nitrate in groundwater occur only locally, and its presence in an individual water supply is chiefly a function of its proximity to sources of contamination, of well construction, and of thickness of overburden. Thirty public-supply wells did have water that had high sodium concentrations or objectionable iron and manganese concentrations, but these are not considered health hazards in the concentrations found in the water samples. Streams, wetlands, and some aquifers along the sough boundary of the basin contain salty water because of tidal movement or extensive ground-water withdrawals. High sediment concentrations also occur as a result of tidal influence in this area.

Connecticut

Fluorine, fluorite, and fluorspar in central Colorado

Fluorine (F) is a widespread element that was deposited in a variety of rocks, minerals, and geologic environments in central Colorado. It occurs as a trace element, as a major component of the mineral fluorite (CaFs), and as a major economic source of fluorine in fluorspar deposits, which are massive concentrations of fluorite. This study has compiled available geochemical analyses of rocks, both unmineralized and mineralized, to determine the distribution of fluorine in specific age-lithologic categories, ranging from 1.8-giga-annum (Ga) metamorphic rocks to modern soils, throughout central Colorado. It also draws upon field studies of fluorine-rich mineral deposits, including fluorspar deposits, to decipher the nearly two-billion-year-long geologic history of fluorine in the study area, with implications for mineral-resource evaluations and exploration. The resulting compilation provides an important inventory of the naturally occurring levels and sources of fluorine that ultimately weather, erode, and become part of surface waters that are used for domestic water supplies in densely populated areas along the Colorado Front Range. Most commonly, fluorine is a trace element in virtually all rocks in the region. In the 3,798 unmineralized rocks that were analyzed for fluorine in the study area, the average fluorine content was 1,550 parts per million (ppm). The median was 640 ppm, nearly identical to the average crustal abundance of 650 ppm, and some high-fluorine rocks in the Pikes Peak area skewed the average to a value much greater than the median. Most unmineralized age-lithologic rock suites, including Proterozoic metamorphic rocks, 1.7- and 1.4-Ga granitic batholiths, Cambrian igneous rocks, Phanerozoic sedimentary rocks, and Laramide and Tertiary igneous rocks, had median fluorine values of 400 to 740 ppm fluorine. In all suites, however, a small number of analyzed samples contained more than 1 percent (10,000 ppm) fluorine. The 1.1-Ga plutonic rocks related to the Pikes Peak batholith had a mean fluorine content of 1,700 ppm, and primary magmatic fluorite and fluorite-bearing pegmatites are common throughout that igneous mass. Fluorine was deposited in many types of economic mineral deposits in central Colorado, and it currently is a significant trace element in some thermal springs. In the fluorspar deposits, fluorine contents were as high as 37 percent. Some fluorine-rich porphyry systems, such as Jamestown, had fluorine values that ranged from 200 ppm to nearly 37 percent fluorine, and veins in other deposits contained hydrothermal fluorite, although it was not ubiquitous. For the 495 samples from non-fluorspar mining districts (and excluding Jamestown), however, the median fluorine content was 990 ppm. This is above the crustal average but still relatively modest compared to the fluorspar deposits, and it indicates that the majority of the mineralizing systems in central Colorado did not deposit large amounts of fluorine. Nevertheless, the fluorine- and fluorite-rich mineral deposits could be used as guides for the evaluation and discovery of related but concealed porphyry and epithermal base- and precious-metal deposits. The Cenozoic geologic history of central Colorado included multiple periods during which fluorine-bearing rocks and mineral deposits were exposed, weathered, and eroded. This protracted history has released fluorine into soils and regoliths, and modern rainfall and snowmelt interact with these substrates to add fluorine to the hydrosphere. This study did not evaluate the fluorine contents of water or make any predictions about what areas might be major sources for dissolved fluorine. However, the abundant data that are available on fluorine in surface water and ground water can be coupled with the results of this study to provide additional insight into natural sources of fluorine in domestic drinking water.

Scientific Investigations Report