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At least 415 records · Page 23Linked to original sources
USGS2024

Measurement of fundamental illite particle thicknesses by X-ray diffraction using PVP-10 intercalation

The thicknesses of fundamental illite particles that compose mixed-layer illite-smectite (I-S) crystals can be measured by X-ray diffraction (XRD) peak broadening techniques (Bertaut-Warren-Averbach [BWA] method and integral peak-width method) if the effects of swelling and XRD background noise are eliminated from XRD patterns of the clays. Swelling is eliminated by intercalating Na-saturated I-S with polyvinylpyrrolidone having a molecular weight of 10,000 (PVP-10). Background is minimized by using polished metallic silicon wafers cut perpendicular to (100) as a substrate for XRD specimens, and by using a single-crystal monochromator. XRD measurements of PVP-intercalated diagenetic, hydrothermal and low-grade metamorphic I-S indicate that there are at least 2 types of crystallite thickness distribution shapes for illite fundamental particles, lognormal and asymptotic; that measurements of mean fundamental illite particle thicknesses made by various techniques (Bertant-Warren-Averbach, integral peak width, fixed cation content, and transmission electron microscopy [TEM]) give comparable results; and that strain (small differences in layer thicknesses) generally has a Gaussian distribution in the log-normal-type illites, but is often absent in the asymptotic-type illites.

Clays and Clay Minerals↗
USGS2024

Effect of illite particle shape on cesium sorption

Samples containing illite and illite-smectite, having different crystal shapes (plates, “barrels”, and filaments), were selected for sorption experiments with cesium. There is a positive correlation between total surface area and Cs-sorption capacity, but no correlation between total surface area and the distribution coefficient, K d . Generally K d increases with the edge surface area, although “hairy” (filamentous) illite does not fit this pattern, possibly because elongation of crystals along one axis reduces the number of specific sorption sites.

Clays and Clay Minerals↗
USGS2024

Ordovician and Pennsylvanian berthierine-bearing flint clays

We report here the first occurrence of berthierine-bearing flint clays, one Ordovician and one Pennsylvanian in age. They are characterized by a berthierine-kaolinite-boehmite (bkb) assemblage. The Pennsylvanian flint clay from northeastern Kentucky is more typical in that it occurs in association with coal measures. The Ordovician occurrence from northwestern Illinois is the oldest flint clay of which we are aware. Because it is Ordovician, it formed before the evolution of terrestrial vascular plants. All previous reports of flint clays point to a genetic connection between flint-clay formation and the growth and decay of plants (Bohor and Triplehorn, 1993). Except for the high berthierine content and greenish color, the physical properties of this flint clay are similar to those of other kaolinitic flint clays. Some samples of the Ordovician flint clay are nearly pure berthierine.

Clays and Clay Minerals↗
USGS2024

Characterization of microbially Fe(III)-reduced nontronite: Environmental cell-transmission electron microscopy study

Microstructural changes induced by the microbial reduction of Fe(III) in nontronite by Shewanella oneidensis were studied using environmental cell (EC)-transmission electron microscopy (TEM), conventional TEM, and X-ray powder diffraction (XRD). Direct observations of clays by EC-TEM in their hydrated state allowed for the first time an accurate and unambiguous TEM measurement of basal layer spacings and the contraction of layer spacing caused by microbial effects, most likely those of Fe(III) reduction. Non-reduced and Fe(III)-reduced nontronite, observed by EC-TEM, exhibited fringes with mean d 001 spacings of 1.50 nm (standard deviation, σ = 0.08 nm) and 1.26 nm (σ = 0.10 nm), respectively. In comparison, the same samples embedded with Nanoplast resin, sectioned by microtome, and observed using conventional TEM, displayed layer spacings of 1.0–1.1 nm (non-reduced) and 1.0 nm (reduced). The results from Nanoplast-embedded samples are typical of conventional TEM studies, which have measured nearly identical layer spacings regardless of Fe oxidation state. Following Fe(III) reduction, both EC- and conventional TEM showed an increase in the order of nontronite selected area electron diffraction patterns while the images exhibited fewer wavy fringes and fewer layer terminations. An increase in stacking order in reduced nontronite was also suggested by XRD measurements. In particular, the ratio of the valley to peak intensity ( v/p ) of the 1.7 nm basal 001 peak of ethylene glycolated nontronite was measured at 0.65 (non-reduced) and 0.85 (microbially reduced).

Clays and Clay Minerals↗
USGS2024

Determination of layer-charge characteristics of smectites

A new method for calculation of layer charge and charge distribution of smectites is proposed. The method is based on comparisons between X-ray diffraction (XRD) patterns of K-saturated, ethylene glycol-solvated, oriented samples and calculated XRD patterns for three-component, mixed-layer systems. For the calculated patterns it is assumed that the measured patterns can be modeled as random interstratifications of fully expanding 17.1 Å layers, partially expanding 13.5 Å layers and non-expanding 9.98 Å layers. The technique was tested using 29 well characterized smectites. According to their XRD patterns, smectites were classified as group 1 (low-charge smectites) and group 2 (high-charge smectites). The boundary between the two groups is at a layer charge of −0.46 equivalents per half unit-cell. Low-charge smectites are dominated by 17.1 Å layers, whereas high-charge smectites contain only 20% fully expandable layers on average. Smectite properties and industrial applications may be dictated by the proportion of 17.1 Å layers present. Non-expanding layers may control the behavior of smectites during weathering, facilitating the formation of illite layers after subsequent cycles of wetting and drying. The precision of the method is better than 3.5% at a layer charge of −0.50; therefore the method should be useful for basic research and for industrial purposes.

Clays and Clay Minerals↗
USGS2024

Thickness distributions and evolution of growth mechanisms of NH4-illite from the fossil hydrothermal system of Harghita Bai, Eastern Carpathians, Romania

The crystal growth of NH 4 -illite (NH 4 -I) from the hydrothermal system of Harghita Bãi (Eastern Carpathians) was deduced from the shapes of crystal thickness distributions (CTDs). The 4-illite-smectite (I-S) interstratified structures (R1, R2, and R3-type ordering) with a variable smectite-layer content. The NH 4 -I-S (40–5% S) structures were identified underground in a hydrothermal breccia structure, whereas the K-I/NH 4 -I mixtures were found at the deepest level sampled (−110 m). The percentage of smectite interlayers generally decreases with increasing depth in the deposit. This decrease in smectite content is related to the increase in degree of fracturing in the breccia structure and corresponds to a general increase in mean illite crystal thickness. In order to determine the thickness distributions of NH 4 -I crystals (fundamental illite particles) which make up the NH 4 -I-S interstratified structures and the NH 4, -I/K-I mixtures, 27 samples were saturated with Li + and aqueous solutions of PVP-10 to remove swelling and then were analyzed by X-ray diffraction. The profiles for the mean crystallite thickness (T mean ) and crystallite thickness distribution (CTD) of NH 4 -I crystallites were determined by the Bertaut-Warren-Averbach method using the MudMaster computer code. The T mean of NH 4 -I from NH 4 -I-S samples ranges from 3.4 to 7.8 nm. The T mean measured for the NH 4 -I/K-I mixture phase ranges from 7.8 nm to 11.7 nm (NH 4 -I) and from 12.1 to 24.7 nm (K-I). The CTD shapes of NH 4 -I fundamental particles are asymptotic and lognormal, whereas illites from NH 4 -I/K-I mixtures have bimodal shapes related to the presence of two lognormal-like CTDs corresponding to NH 4 -I and K-I. The crystal-growth mechanism for NH 4 -I samples was simulated using the Galoper code. Reaction pathways for NH 4 -I crystal nucleation and growth could be determined for each sample by plotting their CTD parameters on an α–β 2 diagram constructed using Galoper . This analysis shows that NH 4 -I crystals underwent simultaneous nucleation and growth, followed by surface-controlled growth without simultaneous nucleation.

Harghita Bai↗
USGS1973

Stable isotope and chemical relations during mineralization in the Bodie mining district, Mono County, California

Stable isotope and chemical relations have been determined in a typical epithermal Au-Ag deposit located in the Bodie mining district of California. Analyses were made of altered host rocks, vein minerals, alteration clays, fluid inclusions, modern spring waters, and unaltered rocks of the area.The results indicate that a hydrothermal convection system was set up by the interaction of a cooling shallow intrusion and local meteoric water. The water traveled to depth where it picked up ore constituents and SiO 2 , K, and Rb, without significant shifts in the stable isotope ratios of the water. The altered rocks have equilibrated to various degrees with an ore fluid of constant K/Rb, O 18 /O 16 and D/H ratios. Deposition of ore took place over the approximate temperature range 215 degrees -245 degrees . From C 13 /C 12 ratios of minor calcite, a volcanic source of CO 2 is postulated. The chemical and isotope composition of the ore fluid is strikingly similar to that of modern spring waters in the area.All ore deposition at Bodie took place from essentially isotopically unaltered ground water with delta O 18 = -13ppm and delta D = -98ppm.

California↗
USGS1983

Mineral resource potential map of the Natural Area Roadless Area, Baker County, Florida

The Natural Area Roadless Area, which is in the Osceola National Forest in Baker County, Fla., is underlain by sedimentary rocks containing phosphate deposits that are not a potential mineral resource by todays standards. The region has a low potential for oil and gas and virtually no potential for other valuable minerals. The phosphate deposits are either slightly low in tonnage and P 2 O 5 content, high in MgO and/or Fe 2 O 3 + Al 2 O 3 , or the ratio of CaO to P 2 O 5 is too high for deposits that can be mined profitably at the present time. A low potential for oil and gas is indicated by the numerous dry holes in the region and the absence of the formations that contain these hydrocarbons in southern and westernmost Florida. The only mineral material that has been produced in the study area is clayey sand, used in stabilizing Forest Service roads. This type of clayey sand has no particular value because there are virtually unlimited quantities in the surrounding region. The peaty material in the area is too high in ash content to be mined. Large quantities of limestone underlie the area but are too deeply buried to be quarried. Heavy-mineral and clay deposits, which are mined elsewhere in northern peninsular Florida, are not present in the study area.

Florida↗
USGS2007

Insight into the geology of the East Antarctic hinterland: a study of sediment inclusions from ice cores of the Lake Vostok borehole

The borehole at the southern part of subglacial Lake Vostok has been drilled into an ice layer that has been refrozen from the lake water. This ice layer contains random sediment inclusions, eight of which have been studied using state-of the-art analytical techniques. Six inclusions comprise soft aggregates consisting mainly of clay-mica minerals and micron-sized quartz grains while two others are solid clasts of fine-grained cemented rocks. The largest rock clast consists of poorly-rounded quartz and minor amounts of accessory minerals and is classified as quartzose siltstone. More than twenty grains of zircon and monazite have been identified in this siltstone and dated by SIMS SHRIMP-II. Two age clusters have been recognized for these detrital grains, in the ranges 0.8−1.2 Ga and 1.6−1.8 Ga. The compositions of the rock clasts suggest that the bedrock situated to the west of Lake Vostok is sedimentary. The age data on the detrital accessory minerals suggest that the provenance of these sedimentary rocks − the Gamburtsev Mountains and Vostok Subglacial Highlands, is mainly represented by Paleoproterozoic and MesoproterozoicNeoproterozoic crustal provinces

Open-File Report↗
USGS1996

Initiation and frequency of debris flows in Grand Canyon, Arizona

Debris flows occur in 600 tributaries of the Colorado River in Grand Canyon, Arizona when intense precipitation causes slope failures in bedrock or colluvium. These slurries transport poorly sorted sediment, including very large boulders that form rapids at the mouths of tributaries and control the longitudinal profile of the Colorado River. Although the amount of rainfall on the days of historic debris flows typically is not unusual, the storm rainfall on consecutive days before the debris flows typically had recurrence intervals greater than 10 yrs. Four types of failure mechanisms initiate debris flows: bedrock failure (12 percent), failure of colluvial wedges by rainfall (21 percent), failure of colluvial wedges by runoff (the "firehose effect;" 36 percent), and combinations of these failure mechanisms (30 percent). Failure points are directly or indirectly associated with terrestrial shales, particularly the Permian Hermit Shale, shale units within the Permian Esplanade Sandstone of the Supai Group, and the Cambrian Bright Angel Shale. Shales either directly fail, produce colluvial wedges downslope that contain clay, or form benches that store poorly sorted colluvium in wedge-shaped deposits. Terrestrial shales provide the fine particles and clay minerals-particularly kaolinite and illite-essential to long-distance debris-flow transport, whereas marine shales mostly contain smectites, which inhibit debris-flow initiation. Using repeat photography, we determined whether or not a debris flow occurred in the last century in 164 of 600 tributaries in Grand Canyon. We used logistic regression to model the binomial frequency data using 21 morphometric and lithologic variables. The location of shale units, particularly the Hermit Shale, within the tributary is the most consistent variable related to debris-flow frequency in Grand Canyon. Other statistically significant variables vary with large scale changes in canyon morphology. Standard morphometric measures such as drainage-basin area, channel gradient, and aspect of the river corridor are the most significant variables in the narrow and deep eastern section of Grand Canyon. Measures of the location of source lithologies are more important in western Grand Canyon, which has broader and low-gradient drainages. Measures of geologic structure, and other standard hydrologic variates, were not significant. Our results show that the probability of debris-flow occurrence is highest in eastern Grand Canyon. Throughout Grand Canyon, the probability of debris-flow occurrence is highest in reaches of the Colorado River that trend south-southwest. This direction is significant because most summer storms originate from a southerly direction, and the maximum slope of the regional structure is to the southwest. The binomial frequency of debris flows is not random in Grand Canyon, and tributaries of similar debris-flow frequency are clustered in distinct reaches.

Arizona↗
USGS1996

Summary of the Oahu, Hawaii, regional aquifer-system analysis

Oahu, the third largest of the Hawaiian islands, is formed by the eroded remnants of two elongated shield volcanoes with broad, low profiles. Weathering and erosion have modified the original domed surfaces of the volcanoes, leaving a landscape of deep valleys and steep interfluvial ridges in the interior highlands. The Koolau Range in eastern Oahu and the Waianae Range in western Oahu are the eroded remnants of the Koolau and Waianae Volcanoes. The origin, mode of emplacement, texture, and composition of the rocks of Oahu affect their ability to store and transmit water. The volcanic rocks are divided into four groups: (1) lava flows, (2) dikes, (3) pyroclastic deposits, and (4) saprolite and weathered basalt. Stratified sequences of thin-bedded lava flows form the most productive aquifers in Hawaii. Dikes are near-vertical sheets of massive intrusive rock that typically contain only fracture permeability. Pyroclastic deposits include ash, cinder, and spatter; they are essentially granular, with porosity and permeability similar to those of granular sediments. Weathering of basaltic rocks in the humid, subtropical climate of Oahu alters igneous minerals to clays and oxides, reducing the permeability of the parent rock. Saprolite is weathered material that has retained textural features of the parent rock. Estimates of hydraulic conductivity along the plane of dike-free lava flows tend to fall within about one order of magnitude, from about 500 to about 5,000 feet per day. Estimates of specific yield range from about 1 to 20 percent; most of the values lie within a narrow range of about 5 to 10 percent. The occurrence of ground water on Oahu is determined by the type and character of the rocks and by the presence of geohydrologic barriers. The primary modes of freshwater occurrence on Oahu are as a basal lens of fresh ground water floating on saltwater, as dike-impounded ground water, and as perched ground water. Saltwater occurs at depth throughout much of the island. A regional aquifer system composed of the Waianae aquifer in the Waianae Volcanics and the Koolau aquifer in the Koolau Basalt is subdivided into well-defined areas by geohydrologic barriers. The aquifers are separated by the Waianae confining unit formed by weathering along the Waianae-Koolau unconformity. In some coastal areas, a caprock of sedimentary deposits overlies and confines the aquifers. The island of Oahu has been divided into seven major ground-water areas delineated by deep-seated structural geohydrologic barriers; these areas are further subdivided by shallower internal barriers to ground-water flow. The Koolau rift zone along the eastern (windward) side of the island and the Waianae rift zone to the west (Waianae area) constitute two of the major ground-water areas. North-central Oahu is divided into three smaller ground-water areas, Mokuleia, Waialua, and Kawailoa. The Schofield ground-water area encompasses much of the Schofield Plateau of central Oahu. Southern Oahu is divided into six areas, Ewa, Pearl Harbor, Moanalua, Kalihi, Beretania, and Kaimuki. Southeastern Oahu is divided into the Waialae and Wailupe-Hawaii Kai areas. Along the northeast coast of windward Oahu is the Kahuku ground-water area. The aquifers of Oahu contain shallow freshwater and deeper saltwater flow systems. There are five fresh ground-water flow systems: meteoric freshwater flow diverges from ground-water divides that lie somewhere within the Waianae and Koolau rift zones, forming an interior flow system in central Oahu (which is divided into the northern and southern Oahu flow systems) and exterior flow systems in western (Waianae area) Oahu, eastern (windward) Oahu, and southeastern Oahu. Development of the ground-water resources on Oahu began when the first well was drilled near Honouliuli in the summer of 1879. By 1890, 86 wells had been drilled on the island. From about 1891 to about 1910, development increased rapidly with the drilling of a

Hawaii↗
USGS2022

Evaluation of salinity and nutrient conditions in the Heart River Basin, North Dakota, 1970–2020

The Heart River Basin is predominantly an agricultural basin in western North Dakota and is approximately 3,350 square miles. The U.S. Geological Survey, in cooperation with the U.S. Department of Agriculture Natural Resources Conservation Service and the Grant County Soil Conservation District, completed a study to assess spatial and temporal patterns of water quality in the Heart River Basin. The purpose of this report is to describe the methods and results of a study to evaluate salinity and nutrients in the Heart River Basin in western North Dakota. Water-quality and streamflow data used in the study were compiled from 1970 to 2020 using the National Water Quality Monitoring Council Water Quality Portal and National Water Information System. Changes in streamflow characteristics were investigated at three sites from 1970 to 2020, and changes in water quality were investigated at four sites from 1974 to 2019. Streamflow analysis indicated decreasing streamflow from 1970 until the late 1990s followed by increasing streamflow through 2020, with the largest increase in the 7-day minimum streamflow or base flow. For the historical water-quality trend period (1974–2019), total dissolved solids, sulfate, sodium, chloride, and sodium adsorption ratio concentrations have increased since the mid-1970s through 2019. Potassium concentrations during the historical period remained mostly constant with some small fluctuations. Calcium and magnesium concentrations increased since the mid-1970s at all sites, except for a decrease at one site between 1974 and 1999. During the recent trend period (1999–2019), increasing concentrations in total dissolved solids, sulfate, sodium, chloride, calcium, magnesium, and sodium adsorption ratios were observed across the Heart River Basin. The magnitude of the increases was smaller at tributary sites compared to main-stem sites. During the recent period, potassium was mostly constant, although small (−0.9 milligram per liter or less) decreases on tributaries and minor (1.3 milligrams per liter) increases on the main-stem sites were detected. Unlike dissolved ion concentrations, significant increases in nutrient concentrations were not detected from 1999 to 2019, but nitrate plus nitrite concentrations most likely decreased upstream from Lake Tschida. Inverse modeling for period 1 (1974–99) in model zone 1 (Heart River reach from site 5 to site 6) had eight reasonable models that indicated the clay mineral-water interactions and dissolution of evaporites control the geochemistry. Results of the inverse modeling for period 2 (1999–2019) in model zone 1 also had eight reasonable models that indicated that the dissolution of evaporites was the major geochemical control. Results of the geochemical modeling for period 1 (1974–99) in model zone 2 (Heart River and Sweetbriar Creek reach from sites 20 and 21 to site 22) produced seven reasonable models, and the geochemical control of the system was the dissolution of sulfate evaporite minerals. Geochemical modeling results for period 2 (1999–2019) in model zone 2 produced 11 reasonable models and was also controlled by the dissolution of sulfate evaporite minerals. Differences between the two model zones indicated that geology controls some of the water-quality changes in the Heart River Basin. Loads were estimated for total dissolved solids, sulfate, sodium, and chloride and total phosphorus. Annual loads estimated for the Heart River from 2013 through 2020 at the Heart River site upstream from Lake Tschida (site 5) and near Mandan (site 22) were generally greatest in 2014 and least in 2016 for total dissolved solids, sulfate, sodium, and chloride. Most of the annual loads of total dissolved solids, sulfate, sodium, and chloride are delivered in March through July in the Heart River at these sites and are likely from snowmelt and spring and summer rains. The mean annual yields of total dissolved solids and sodium from 2013 to 2020 generally were largest in Big Muddy Creek (site 18), whereas yields of sulfate and chloride were largest at Sweetbriar Creek (site 21) compared to the other selected sites in the Heart River Basin. Larger yields of total dissolved solids, sulfate, sodium, and chloride at sites located on Big Muddy Creek and Sweet Briar Creek in the lower Heart River Basin were likely a result of differences in geology and soils upstream from the selected sites. A mass balance of total dissolved solids, sulfate, sodium, and chloride was estimated for the lower Heart River Basin, specifically the reach below Lake Tschida to Mandan (site 7 to site 22). Intervening flow was the largest contributor to the dissolved ion loads in the lower Heart River Basin and is an important part of understanding the transport of dissolved ions in the basin. The intervening load can include groundwater discharge, irrigation return flow, local runoff, and input from smaller ephemeral tributaries. Tributaries in the lower Heart River Basin contributed portions of the total dissolved solids, sulfate, sodium, and chloride loads at the Heart River near Mandan (site 22) that generally were proportional to the streamflow contributions. Annual loads for total phosphorus between 2013 and 2020 at the Heart River site upstream from Lake Tschida (site 5) and near Mandan (site 22) generally were largest in 2019 and smallest in 2016. Most of the total phosphorus loads for main-stem sites 5 and 22 were transported in March, April, and June, likely from snowmelt and early summer rains. The mean annual yields of total phosphorus for 2013–20 were largest on the main-stem site upstream from Lake Tschida (site 5) and Sweetbriar Creek (site 21), whereas the smallest yields were in Big Muddy Creek (site 18). Much of the phosphorus that enters Lake Tschida from the upper basin does not get transported downstream to the lower basin, and much of the phosphorus in the lower basin was attributed to intervening flow.

North Dakota↗
USGS1976

Mineral-produced high-pressure striae and clay polish: Key evidence for nonballistic transport of ejecta from Ries crater

Recently discovered mineral-produced, deeply incised striae and mirror-like polish on broken surfaces of limestone fragments from the sedimentary ejecta of the Ries impact crater of southern Germany are described. The striae and polish were produced under high confining pressures during high-velocity nonballistic transport of the ejecta mass within the time span of the cratering event (measured in terms of seconds). The striae on these fragments were produced by scouring by small mineral grains embedded in the surrounding clay matrix, and the polish was formed under the same condition, by movements of relatively fragment-free clay against the fragment surfaces. The occurrence of these striae and polish is key evidence for estimating the distribution and determining the relative importance of nonballistic and ballistic transport of ejecta from the shallow Ries stony meteorite impact crater.

southern Germany↗
USGS2012

Lithostratigraphy from downhole logs in Hole AND-1B, Antarctica

The ANDRILL (Antarctic Drilling Project) McMurdo Ice Shelf (MIS) project drilled 1285 m of sediment in Hole AND–1B, representing the past 12 m.y. of glacial history. Downhole geophysical logs were acquired to a depth of 1018 mbsf (meters below seafloor), and are complementary to data acquired from the core. The natural gamma radiation (NGR) and magnetic susceptibility logs are particularly useful for understanding lithological and paleoenvironmental change at ANDRILL McMurdo Ice Shelf Hole AND–1B. NGR logs cover the entire interval from the seafloor to 1018 mbsf, and magnetic susceptibility and other logs covered the open hole intervals between 692 and 1018 and 237–342 mbsf. In the upper part of AND–1B, clear alternations between low and high NGR values distinguish between diatomite (lacking minerals containing naturally radioactive K, U, and Th) and diamictite (containing K-bearing clays, K-feldspar, mica, and heavy minerals). In the lower open hole logged section, NGR and magnetic susceptibility can also distinguish claystones (rich in K-bearing clay minerals, relatively low in magnetite) and diamictites (relatively high in magnetite). Sandstones can be distinguished by their high resistivity values in AND–1B. On the basis of these three downhole logs, diamictite, claystones, and sandstones can be predicted correctly for 74% of the 692–1018 mbsf interval. The logs were then used to predict facies for the 6% of this interval that was unrecovered by coring. Given the understanding of the physical property characteristics of different facies, it is also possible to identify subtle changes in lithology from the physical properties and help refine parts of the lithostratigraphy, for example, the varying terrigenous content of diatomites and the transitions from subice diamictite to open-water diatomite.

Geosphere↗
USGS2017

Evolution of soils on quaternary reef terraces of Barbados, West Indies

Soils on uplifted Quaternary reef terraces of Barbados, ???125,000 to ???700,000 yr old, form a climo-chronosequence and show changes in physical, chemical, and mineralogical properties with terrace age. Parent materials are dust derived from the Sahara, volcanic ash from the Lesser Antilles island arc, and detrital carbonate from the underlying reef limestone. Although some terrace soils are probably eroded, soils or their remnants are redder and more clay-rich with increasing terrace age. Profile-average Al2O3 and Fe2O3 content increases with terrace age, which partially reflects the increasing clay content, but dithionite-extractable Fe also increases with terrace age. Profile-average K2O/TiO2, Na2O/TiO2, and P2O5/TiO2 values decrease with terrace age, reflecting the depletion of primary minerals. Average SiO2/Al2O3 values also decrease with terrace age and reflect not only loss of primary minerals but also evolution of secondary clay minerals. Although they are not present in any of the parent materials, the youngest terrace soils are dominated by smectite and interstratified kaolinite-smectite, which gradually alter to relatively pure kaolinite over ???700,000 yr. Comparisons with other tropical islands, where precipitation is higher and rates of dust fall may be lower, show that Barbados soils are less weathered than soils of comparable age. It is concluded that many soil properties in tropical regions can be potentially useful relative-age indicators in Quaternary stratigraphic studies, even when soils are eroded or changes in soil morphology are not dramatic. ?? 2001 University of Washington.

Quaternary Research↗
USGS2003

Ball clay

Part of the 2002 industrial minerals review. Statistics on ball clay consumption, production, prices, trade, and trends are presented.

Mining Engineering↗
USGS1989

Geochemistry of the Floridan aquifer system in Florida and in parts of Georgia, South Carolina, and Alabama

The chemical quality of the ground water in the Floridan aquifer system is determined primarily by mineral-water interaction. However, some changes in water quality have been imposed by development, particularly near coastal pumping centers. A total of 601 chemical analyses, all from different wells, most completed in the upper part of the aquifer system, were used to describe the variations in water chemistry and to study the processes responsible for observed changes. The Floridan aquifer system is a vertically continuous sequence of Tertiary carbonate rocks that are of generally high permeability and are hydraulically connected in varying degrees. The rocks are principally limestone and dolomite, but they grade into limy sands and clays near the aquifer system's updip limits. Major minerals in the aquifer system are calcite, dolomite, and, locally, gypsum or quartz; minor minerals include apatite, glauconite, and clay minerals such as kaolinite and montmorillonite. Trace amounts of metallic oxides or sulfides are present in some areas. The aquifer system consists of the Upper and Lower Floridan aquifers, separated in most places by a less permeable confining unit that has highly variable hydraulic properties. Only the Upper Floridan aquifer is present throughout the study area. Freshwater enters the aquifer system in outcrop areas located primarily in central Georgia and north-central Florida. Discharge occurs chiefly to streams and springs and, to a lesser extent, directly into the sea. Most of the flow into and out of the system takes place where it is unconfined or where the upper confining unit is thin. Secondary permeability developed by dissolution of aquifer material is most prominent in these areas of dynamic flow. Dissolved-solids concentrations in water from the Upper Floridan aquifer generally range from less than 25 milligrams per liter near outcrops to more than 25,000 milligrams per liter along the coasts. The dominant cations in the ground water are Ca2+, Mg2+, and Na+; the dominant anions are HCO3-, Cl-, and SO42-, The concentration of Ca2+ is controlled primarily by calcite saturation. Concentrations of Mg2+, NA+, and Cl- are highest where mixing of freshwater and saltwater occurs. Concentrations of HCO3- reflect the control of calcite solubility. The concentration of SO42- is highest where gypsiferous rock units are present in the aquifer system. The major geochemical processes that occur in the Upper Floridan aquifer, based on water-quality maps and computations using a geochemical model, are (1) dissolution of aquifer minerals toward equilibrium, (2) mixing of ground water with recharge, leakage, or seawater, (3) sulfate reduction, and (4) cation exchange between water and aquifer minerals. Similar processes apparently control minor dissolved constituents, although quantification is difficult with the available data. Statistical tests of available nutrient data indicate that concentrations of N (nitrogen) species in unconfined recharge areas may be increasing over time; more detailed studies of all N species are needed to test this hypothesis, however. Data on trace metals, radionuclides, and man-made organic contaminants are limited. Available data indicate that most freshwater within the Upper Floridan is potable, but detection of pesticides in a few samples indicates that the system is susceptible to contamination from the land surface in some areas, particularly where its upper confining unit is thin or absent. Geochemical models were used to examine changes in major chemical elements along selected ground-water paths within the Upper Floridan aquifer. Water in the Upper Floridan aquifer can be categorized into four hydrochemical facies, whose exact distribution is determined by confined or unconfined conditions of the aquifer and by chloride concentrations. The reaction models are considered plausible based on available chemical, isotopic, and hydrologic information, and they

Alabama, Florida, Georgia, South Carolina↗