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At least 577 records · Page 32Linked to original sources

USGS2014

Geology and total petroleum systems of the Paradox Basin, Utah, Colorado, New Mexico, and Arizona

The geological model for the development of the Total Petroleum Systems (TPSs) within the Paradox Basin formed the foundation of the recent U.S. Geological Survey assessment of undiscovered, technically recoverable resources in the basin. Five TPSs were defined, of which three have known production and two are hypothetical. These TPSs are based on geologic elements of the basin and the potential development of Precambrian, Devonian, Pennsylvanian, Permian-Mississippian, and Cretaceous source rock intervals. The most studied source intervals are the Pennsylvanian black shales that were deposited during relative high stands in an otherwise evaporitic basin. These black shales are the source for most of the discovered hydrocarbons in the Paradox Basin. A second oil type can be traced to either a Mississippian or Permian source rock to the west, and therefore requires long-distance migration to explain its presence in the basin. Upper Cretaceous continental to nearshore-marine sandstones are interbedded with coal beds that have recognized coalbed methane potential. Precambrian and Devonian TPSs are considered hypothetical, as both are known to have organic-rich intervals, but no discovered hydrocarbons have been definitively typed back to either of these units.

Arizona, Colorado, New Mexico, Utah↗

USGS2016

Are the Columbia River Basalts, Columbia Plateau, Idaho, Oregon, and Washington, USA, a viable geothermal target? A preliminary analysis

The successful development of a geothermal electric power generation facility relies on (1) the identification of sufficiently high temperatures at an economically viable depth and (2) the existence of or potential to create and maintain a permeable zone (permeability >10 -14 m 2 ) of sufficient size to allow efficient long-term extraction of heat from the reservoir host rock. If both occur at depth under the Columbia Plateau, development of geothermal resources there has the potential to expand both the magnitude and spatial extent of geothermal energy production. However, a number of scientific and technical issues must be resolved in order to evaluate the likelihood that the Columbia River Basalts, or deeper geologic units under the Columbia Plateau, are viable geothermal targets. Recent research has demonstrated that heat flow beneath the Columbia Plateau Regional Aquifer System may be higher than previously measured in relatively shallow (<600 m depth) wells, indicating that sufficient temperatures for electricity generation occur at depths 5 km. The remaining consideration is evaluating the likelihood that naturally high permeability exists, or that it is possible to replicate the high average permeability (approximately 10 -14 to 10 -12 m 2 ) characteristic of natural hydrothermal reservoirs. From a hydraulic perspective, Columbia River Basalts are typically divided into dense, impermeable flow interiors and interflow zones comprising the top of one flow, the bottom of the overlying flow, and any sedimentary interbed. Interflow zones are highly variable in texture but, at depths <600 m, some of them form highly permeable regional aquifers with connectivity over many tens of kilometers. Below depths of ~600 m, permeability reduction occurs in many interflow zones, caused by the formation of low-temperature hydrothermal alteration minerals (corresponding to temperatures above ~35 °C). However, some high permeability (>10-14 m 2 ) interflows are documented at depths up to ~1,400 m. If the elevated permeability in these zones persists to greater depths, they may provide natural permeability of sufficient magnitude to allow their exploitation as conventional geothermal reservoirs. Alternatively, if the permeability in these interflow zones is less than 10-14 m 2 at depth, it may be possible to use hydraulic and thermal stimulation to enhance the permeability of both the interflow zones and the natural jointing within the low-permeability interior portions of individual basalt flows in order to develop Enhanced/Engineered Geothermal System (EGS) reservoirs. The key challenge for an improved Columbia Plateau geothermal assessment is acquiring and interpreting comprehensive field data that can provide quantitative constraints on the recovery of heat from the Columbia River Basalts at depths greater than those currently tested by deep boreholes.

Idaho, Oregon, Washington↗

USGS2010

Geology and undiscovered oil and gas resources in the Madison Group, Williston Basin, North Dakota and Montana

Two of the total petroleum systems (TPS) defined as part of the U.S. Geological Survey (USGS) assessment of the Williston Basin contain Mississippian Madison Group strata: 1) the Bakken-Lodgepole TPS, which includes the Lodgepole Formation; and 2) the Madison TPS, which includes the Mission Canyon, Charles, and Spearfish formations. The Bakken-Lodgepole TPS is defined as the area in which oil generated from the upper and lower shales of the Upper Devonian-Lower Mississippian Bakken Formation has accumulated in reservoirs in the Three Forks, Bakken, and Lodgepole formations. Two conventional assessment units (AU) have been identified within the Bakken-Lodgepole TPS, including one in the Bakken Formation and another in the Waulsortian mound reservoirs of the lower Lodgepole Formation. Lodgepole Formation Waulsortian mound oil production has been restricted to a small part of Stark County, North Dakota. Reservoirs are sealed by middle and upper Lodgepole Formation tight argillaceous limestones. Several nonproductive mounds and mound-like structures have also been identified in the Lodgepole Formation. Productivity correlates closely with the oil window of the Bakken Formation shales, and also indicates the likelihood of limited lateral migration of Bakken Formation oil into Lodgepole Formation reservoirs in North Dakota and Montana. Such considerations limit the estimated mean of undiscovered, technically recoverable resources to 8 million barrels of oil (MMBO) for the Lodgepole Formation conventional reservoirs. The Madison TPS is defined as the area where oil generated from Mission Canyon and Charles formation source rocks has accumulated in reservoirs of the Mission Canyon and Charles formations and in reservoirs within the Triassic Spearfish Formation. One continuous reservoir AU, the Mission Canyon-Charles AU, was defined within the Madison TPS; its boundary coincides with the TPS boundary. There is extensive conventional production throughout the AU on major structures and in stratigraphic-structural traps. The largest fields are on the Little Knife, Billings Nose, and Nesson anticlines. Recent studies show that Madison Group oils were generated from organic-rich Mission Canyon Formation and Ratcliffe Interval carbonates adjacent to the reservoirs. Seals were formed by overlying or lateral evaporites or tight carbonates. Based on available geologic and production data, the undiscovered oil resources for conventional reservoirs in the Mission Canyon-Charles AU were estimated to have a mean of 45 MMBO.

Mountain Geologist↗

USGS2010

A 15 000-year record of climate change in northern New Mexico, USA, inferred from isotopic and elemental contents of bog sediments

Elemental (C, N, Pb) and isotopic ( δ 13 C, δ 15 N) measurements of cored sediment from a small bog in northern New Mexico reveal changes in climate during the Late Pleistocene and Holocene. Abrupt increases in Pb concentration and δ 13 C values ca. 14 420 cal. YBP indicate significant runoff to the shallow lake that existed at that time. Weathering and transport of local volcanic rocks resulted in the delivery of Pb-bearing minerals to the basin, while a 13 C-enriched terrestrial vegetation source increased the δ 13 C values of the sedimentary material. Wet conditions developed over a 300 a period and lasted for a few hundred years. The Younger Dryas period (ca. 12 700–11 500 cal. YBP) caused a reduction in terrestrial productivity reflected in decreasing C/N values, δ 15 N values consistently greater than 0‰ and low organic content. By contrast, aquatic productivity increased during the second half of this period, evidenced by increasing δ 13 C values at the time of highest abundance of algae. Dry conditions ca. 8 000–6 000 cal. YBP were characterised by low organic carbon content and high Pb concentrations, the latter suggesting enhanced erosion and aeolian transport of volcanic rock. The range in δ 13 C, δ 15 N and C/N values in the sedimentary record fall within the range of modern plants, except during the periods of runoff and drought. The sedimentary record provides evidence of natural climate variability in northern New Mexico, including short- (multi-centennial) and long-(millennial) term episodes during the Late Pleistocene and Holocene.

Journal of Quaternary Science↗

USGS2008

Uranium in surface waters and sediments affected by historical mining in the Denver West 1:100,000 Quadrangle, Colorado

Geochemical sampling of 82 stream waters and 87 stream sediments within mountainous areas immediately west of Denver, Colorado, was conducted by the U.S. Geological Survey in October 1994. The primary purpose was to evaluate regionally the effects of geology and past mining on the concentration and distribution of uranium. The study area contains uranium- and thorium-rich bedrock, numerous noneconomic occurrences of uranium minerals, and several uranium deposits of variable size and production history. During the sampling period, local streams had low discharge and were more susceptible to uranium-bearing acid drainage originating from historical mines of base- and precious-metal sulfides. Results indicated that the spatial distribution of Precambrian granites and metamorphic rocks strongly influences the concentration of uranium in stream sediments. Within-stream transport increases the dispersion of uranium- and thorium rich mineral grains derived primarily from granitic source rocks. Dissolved uranium occurs predominantly as uranyl carbonate complexes, and concentrations ranged from less than 1 to 65 micrograms per liter. Most values were less than 5 micrograms per liter, which is less than the current drinking water standard of 30 micrograms per liter and much less than locally applied aquatic-life toxicity standards of several hundred micrograms per liter. In local streams that are affected by uranium-bearing acid mine drainage, dissolved uranium is moderated by dilution and sorptive uptake by stream sediments. Sorbents include mineral alteration products and chemical precipitates of iron- and aluminum-oxyhydroxides, which form where acid drainage enters streams and is neutralized. Suspended uranium is relatively abundant in some stream segments affected by nearby acid drainage, which likely represents mobilization of these chemical precipitates. The 234U/238U activity ratio of acid drainage (0.95-1.0) is distinct from that of local surface waters (more than 1.05), and this distinctive isotopic composition may be preserved in iron-oxyhydroxide precipitates of acid drainage origin. The study area includes a particularly large vein-type uranium deposit (Schwartzwalder mine) with past uranium production. Stream water and sediment collected downstream from the mine's surface operations have locally anomalous concentrations of uranium. Fine-grained sediments downstream from the mine contain rare minute particles (10-20 micrometers) of uraninite, which is unstable in a stream environment and thus probably of recent origin related to mining. Additional rare particles of very fine grained (less than 5 micrometer) barite likely entered the stream as discharge from settling ponds in which barite precipitation was formerly used to scavenge dissolved radium from mine effluent.

Colorado↗

USGS1962

Magnesite and brucite in the United States, exclusive of Alaska and Hawaii

The important deposits of magnesite (MgCO 3 ) and brucite (MgO.H 2 O) in the United States (exclusive of Alaska and Hawaii) are shown on the accompanying map. Single deposits and groups of deposits are shown by geometric symbols according to four size categories based on estimated production plus reserves. These categories are: less than 10,000 tons, 10,000 to 100,000 tons, 100,000 to 1,000,000 tons, and more than 1,000,000 tons. Occurrences of mineralogic interest only are not shown. All map locations are numbered consecutively in each State and keyed to the locality index. The geographical coordinates in the locality index represent the centers of the geometric symbols. Thus, the same coordinates are assigned to all deposits covered by a group symbol. The map was compiled from published reports and data in the files of the United States Geological Survey. The names, geographic coordinates, and geologic types of deposits are given in the locality index. The principal published reports used in compiling the map are listed in the selected references. The main types of commercial deposits of magnesite in the United States are: (1) replacement bodies in limestone and dolomite; (2) replacements and veins in serpentine; and (3) sedimentary beds. Other magnesite deposits of varied origin and less common occurrence include beds associated with talc, chlorite, and mica schists; and veins and lenses in altered tuffs. Brucite is a relatively rare mineral of secondary origin which usually accompanies other magnesian minerals, particularly magnesite and hydromagnesite, and is associated with carbonate rocks and serpentine. Magnesite was first mined in California in 1886, and the State was the only domestic producer until the development of the Washington deposits began in 1916. In recent years, the main production of magnesite has been from Stevens County, Washington, and Nye County, Nevada. Production in California has been intermittent since 1945. Magnesite deposits in Texas were mined during and immediately after World War II. At present (1961) the only brucite deposits being worked are those at Gabbs, Nye County, Nevada. They have been mined almost continuously since 1935.

Mineral Investigations Resource Map↗

USGS1993

International strategic minerals inventory summary report; niobium (columbium) and tantalum

Major world resources of niobium and tantalum are described in this summary report of information in the International Strategic Minerals Inventory (ISMI). ISMI is a cooperative data-collection effort of earth-science and mineral-resource agencies in Australia, Canada, the Federal Republic of Germany, the Republic of South Africa, the United Kingdom, and the United States of America. Part I of this report presents an overview of the resources and potential supply of niobium and tantalum based on inventory information; Part II contains tables of both geologic and mineral-resource information and includes production data collected by ISMI participants. Niobium is used principally as an alloying element in special steels and superalloys, and tantalum is used mainly in electronics. Minerals in the columbite-tantalite series are principal ore minerals of niobium and tantalum. Pyrochlore is a principal source of niobium. These minerals are found in carbonatite, certain rocks in alkaline igneous complexes, pegmatite, and placer deposits. ISMI estimates show that there are over 7 million metric tons of niobium and almost 0.5 million metric tons of tantalum in known deposits, outside of China and the former Soviet Union, for which reliable estimates have been made. Brazilian deposits, followed by Canadian deposits, contain by far the largest source of niobium. Tantalum production is spread widely among several countries, and Brazil and Canada are the most significant of these producers. Brazil's position is further strengthened by potential byproduct columbite from tin mining. Present economically exploitable resources of niobium appear to be sufficient for the near future, but Brazil will continue to be the predominant world supplier of ferrocolumbium. Tantalum, a byproduct of tin production, has been captive to the fluctuations of that market, but resources in pegmatite in Canada and Australia make it likely that future increases in the present modest demand will be met.

Circular↗

USGS2020

Batch extraction method to estimate total dissolved solids (TDS) release from coal refuse and overburden

A rapid batch extraction method was evaluated to estimate potential for total dissolved solids (TDS) release by 65 samples of rock from coal and gas-bearing strata of the Appalachian Basin in eastern USA. Three different extractant solutions were considered: deionized water (DI), DI equilibrated with 10% CO 2 atmosphere (DI + CO 2 ), or 30% H 2 O 2 under 10% CO 2 (H 2 O 2 +CO 2 ). In all extractions, 10 g of pulverized rock (<0.5-mm) were mixed with 20 mL of extractant solution and shaken for 4 h at 50 rpm and 20–22 °C. The 65 rock samples were classified as coal (n=3), overburden (n = 17), coal refuse that had weathered in the field (n = 14), unleached coal refuse that had oxidized during indoor storage (n = 20), gas-bearing shale (n = 10), and pyrite (n = 1). Extracts were analyzed for specific conductance (SC), TDS, pH, and major and trace elements, and subsequently speciated to determine ionic contributions to SC. The pH of extractant blanks decreased in the order DI (6.0), DI + CO 2 (5.1), and H 2 O 2 +CO 2 (2.6). The DI extractant was effective for mobilizing soluble SO 4 and Cl salts. The DI + CO 2 extractant increased weathering of carbonates and resulted in equivalent or greater TDS than the DI leach of the same material. The H 2 O 2 +CO 2 extractant increased weathering of sulfides (and carbonates) and resulted in the greatest TDS production and lowest pH values. Of the 65 samples, 19 had leachate chemistry data from previous column experiments and 35 were paired to 10 field sites with leachate chemistry data. When accounting for the water-to-rock ratio, TDS from DI and DI + CO 2 extractions were correlated to TDS from column experiments while TDS from H 2 O 2 +CO 2 extractions was not. In contrast to column experiments, field SC was better correlated to SC measured from H 2 O 2 +CO 2 extractions than DI extractions. The field SC and SC from H 2 O 2 +CO 2 extractions were statistically indistinguishable for 7 of 9 paired data sets while SC from DI extractions underestimated field SC in 5 of 9 cases. Upscaling comparisons suggest that (1) weathering reactions in the field are more aggressive than DI water or synthetic rainwater extractants used in batch or column tests, and (2) a batch extraction method utilizing 30% H 2 O 2 (which is mildly acidic without CO 2 enrichment) could be effective for identifying rocks that will release high amounts of TDS.

Applied Geochemistry↗

USGS2009

The Sudbury impact layer in the paleoproterozoiciron ranges of northern Michigan, USA

A layer of breccia that contains fragments of impact ejecta has been found at 10 sites in the Paleoproterozoic iron ranges of northern Michigan, in the Lake Superior region of the United States. Radiometric age constraints from events predating and postdating deposition of the breccia are ca. 1875 Ma and 1830 Ma. The major bolide impact that occurred at 1850 Ma at Sudbury, Ontario, 500–700 km east of these sites, is the likely causative event. The Michigan sites described here, along with previously described sites in Minnesota and Ontario, define an extensive ejecta-bearing deposit throughout the Paleoproterozoic iron ranges of the Lake Superior region that we refer to as the Sudbury impact layer. The layer at the sites in Michigan exhibits a range of thicknesses, lithologic characters, and sedimentary settings. The diversity of rock types and internal stratigraphic details of the layer imply that several different processes of transport and deposition are represented, but the detailed investigations needed to document them are incomplete. Many of the sites had been described and interpreted previously as products of common terrestrial processes, but the presence of relict shock-induced planar deformation features in quartz indicates that the breccia layer is in fact the product of an extraterrestrial impact. At most localities, this layer also contains relict fragments of altered devitrified glass and/or accretionary lapilli. One immediate use of the impact layer is as an ultraprecise time line that ties together the well-known stratigraphic sequences of the various geographically separated iron ranges, the correlation of which has remained controversial for many decades. The Sudbury impact layer most commonly lies at a horizon that records a significant change in the character of sediments across the region. The impact layer marks the end of a major period of banded iron formation deposition that was succeeded by deposition of fine clastic rocks, commonly black shales. The impact may have produced regional, if not global, changes in the environment that resulted in this widespread synchronous change in sedimentation style.

Geological Society of America Bulletin↗

USGS2004

The geochemical and magnetic record of coal combustion products in West Virginia reservoir sediments and soils

Western West Virginia lies downwind from numerous coal-fired power plants along the Ohio River Valley. To test whether geochemical and mineralogical impacts from these power plants are detectable on the West Virginia landscape, we obtained reservoir cores, soils, and rocks from two separate sites in West Virginia, one in Harrison County (Hinkel and Deegan Reservoirs) and the other in Roane County (Miletree Run Reservoir). Both have small drainage basins that have the effect of maximizing atmospheric inputs relative to weathering inputs. Sediments from Hinkel Reservoir were dated using the 137 Cs method, and by knowledge of the age of the base of the sedimentary section. Major elements in Hinkel Reservoir sediments do not vary systematically over time, suggesting that the depositional history of these sediments has been relatively constant. In contrast, minor elements and sulfur do show dramatic shifts. Zn, Pb, As, S, Cd, Ge, and Hg all peak during the late 1960s and early 1970s. Polyaromatic hydrocarbons associated with combustion processes likewise show this same behavior. Coincident with these maxima is a peak in isothermal remnant magnetization (IRM), a parameter that is proportional to magnetite abundance. We separated the magnetic fraction of the sediments and examined this fraction petrographically. It is dominated by magnetite with a spherical morphology, which is characteristic of magnetite produced by combustion processes. Chemical analyses on local rocks showed that they were not the likely source for the trace element and magnetite enrichments. To compare soils and reservoir sediments, we normalized geochemical data to Ti; the underlying assumption is that Ti will track physical inputs of soil materials into the reservoir sediments. The normalized sediment data for the elements Zn, Pb, As, and S are all higher for sediments deposited during the late 1960s and early 1970s compared to normalized soil data, implying that soils are not the source for the element enrichments. We thus attribute the enrichment to atmospheric inputs. However, a coal-burning zinc smelter within 10 km of the reservoir site that operated until 1971 may have supplied some or all of the anomalous input: There are no nearby major atmospheric pollution sites near Miletree Run Reservoir. A core from this reservoir was dated based on knowledge of the time it was impounded. Like Hinkel Reservoir, there are no systematic shifts in major element contents over its depositional history. Like Hinkel Reservoir, there are also significant shifts in trace elements and IRM that cannot be explained by local soil sources. Magnetic separates from this reservoir are also dominated by spherical combustion-produced magnetite. Covariance over the period 1930-1980 between magnetite and sulfur with US SO 2 production (which comes dominantly from coal combustion) is strongly suggestive of a significant atmospheric input into Miletree Run Reservoir sediments. The nearest upwind power plants are between 50 and 75 km distant. Thus, relatively long distance transmission of particulate matter from the power plants of the Ohio River Valley is likely in this case.

West Virginia↗

USGS2013

Macroinvertebrate diets reflect tributary inputs and turbidity-driven changes in food availability in the Colorado River downstream of Glen Canyon Dam

Physical changes to rivers associated with large dams (e.g., water temperature) directly alter macroinvertebrate assemblages. Large dams also may indirectly alter these assemblages by changing the food resources available to support macroinvertebrate production. We examined the diets of the 4 most common macroinvertebrate taxa in the Colorado River through Glen and Grand Canyons, seasonally, at 6 sites for 2.5 y. We compared macroinvertebrate diet composition to the composition of epilithon (rock and cliff faces) communities and suspended organic seston to evaluate the degree to which macroinvertebrate diets tracked downstream changes in resource availability. Diets contained greater proportions of algal resources in the tailwater of Glen Canyon Dam and more terrestrial-based resources at sites downstream of the 1st major tributary. As predicted, macroinvertebrate diets tracked turbidity-driven changes in resource availability, and river turbidity partially explained variability in macroinvertebrate diets. The relative proportions of resources assimilated by macroinvertebrates ranged from dominance by algae to terrestrial-based resources, despite greater assimilation efficiencies for algal than terrestrial C. Terrestrial resources were most important during high turbidity conditions, which occurred during the late-summer monsoon season (July–October) when tributaries contributed large amounts of organic matter to the mainstem and suspended sediments reduced algal production. Macroinvertebrate diets were influenced by seasonal changes in tributary inputs and turbidity, a result suggesting macroinvertebrate diets in regulated rivers may be temporally dynamic and driven by tributary inputs.

Arizona↗

USGS2006

Crater gradation in Gusev crater and Meridiani Planum, Mars

The Mars Exploration Rovers investigated numerous craters in Gusev crater and Meridiani Planum during the first ???400 sols of their missions. Craters vary in size and preservation state but are mostly due to secondary impacts at Gusev and primary impacts at Meridiani. Craters at both locations are modified primarily by eolian erosion and infilling and lack evidence for modification by aqueous processes. Effects of gradation on crater form are dependent on size, local lithology, slopes, and availability of mobile sediments. At Gusev, impacts into basaltic rubble create shallow craters and ejecta composed of resistant rocks. Ejecta initially experience eolian stripping, which becomes weathering-limited as lags develop on ejecta surfaces and sediments are trapped within craters. Subsequent eolian gradation depends on the slow production of fines by weathering and impacts and is accompanied by minor mass wasting. At Meridiani the sulfate-rich bedrock is more susceptible to eolian erosion, and exposed crater rims, walls, and ejecta are eroded, while lower interiors and low-relief surfaces are increasingly infilled and buried by mostly basaltic sediments. Eolian processes outpace early mass wasting, often produce meters of erosion, and mantle some surfaces. Some small craters were likely completely eroded/buried. Craters >100 m in diameter on the Hesperian-aged floor of Gusev are generally more pristine than on the Amazonian-aged Meridiani plains. This conclusion contradicts interpretations from orbital views, which do not readily distinguish crater gradation state at Meridiani and reveal apparently subdued crater forms at Gusev that may suggest more gradation than has occurred. Copyright 2006 by the American Geophysical Union.

Journal of Geophysical Research E: Planets↗

USGS2012

Volcanism, isostatic residual gravity and regional tectonic setting of the Cascade volcanic province

A technique to locate automatically boundaries between crustal blocks of disparate densities was applied to upward continued isostatic residual gravity data. The boundary analysis delineates a narrow gravitational trough that extends the length of the Pliocene and Quaternary volcanic arc from Mount Baker in northern Washington to Lassen Peak in California. Gravitational highs interrupt the trough at two localities: a northwest trending high in southern Washington and a northeast trending high between Mount Shasta and Lassen Peak. The latter anomaly is one of a set of northeast trending anomalies that, within the Quaternary arc, appear related to volcanic segmentation proposed previously on the basis of spatial and compositional distributions of volcanoes. These northeast trending anomalies extend hundreds of kilometers northeast of the arc, are caused by sources in the upper crust, and in some cases are related to exposed pre-Tertiary rocks. Segmentation models invoke geometric characteristics of the subducting plate as the primary factor controlling location and chemistry of volcanism, and these northeast trending gravity sources also may be a product of disturbance of the upper crust by the subduction process. More likely, the gravity sources may reflect upper crustal structures older than the High Cascades, possibly relicts from earlier accretionary events or more recent crustal deformation, that have actively influenced the spatial location of more recent volcanism. Much of the Pliocene and Quaternary volcanism of the Cascade arc has concentrated on or near contacts between crustal blocks of disparate density. These contacts may promote the ascension of magma to the Earth's surface.

Journal of Geophysical Research Solid Earth↗

USGS1978

Origin of a South Texas roll-type uranium deposit; I, Alteration of iron-titanium oxide minerals

The detrital Fe-Ti oxide minerals and their authigenic alteration products in samples from cores spanning 1.7 km across a roll-type uranium deposit in the mid-Tertiary Catahoula Tuff, south Texas, record important information on host-rock preparation and on development of the altered tongue of the deposit. In reduced rock, in front of and enveloping the altered tongue, iron disulfide minerals (pyrite and marcasite) have partially to completely replaced titanomagnetite and, to a lesser extent, titanohematite. Subsequent oxidation of these sulfidized Fe-Ti oxides, by processes that formed the altered tongue and uranium roll, produced ferric oxide and hydroxide phases (limonite) pseudomorphous after the sulfides. Fe-Ti oxides 1.0 km updip from the roll front were never sulfidized; titanomagnetite (partly replaced by hematite) and martite constitute nearly half of the heavy mineral fraction and limonite is absent. Oxidized rocks 210 m and closer to the nose of the roll front, however, are nearly devoid of titanomagnetite and contain abundant limonite. The redox interface that bounds the altered tongue, therefore, moved more than 210 m but less than 1.0 km. Detrital Fe-Ti oxide minerals are increasingly sulfidized in the downdip direction indicating that initial sulfidizaton was more intense in that direction. Organic carbon content is uniformly very low throughout the host sandstone, which implies that heterotrophic sulfate-reducing bacteria were not involved in the generation of sulfide. The H 2 S for the initial sulfidization may have been derived from oil and gas in formations that underlie the Catahoula Tuff. The H 2 S probably invaded the Catahoula along a fault that is 1.5 km downdip from the present roll front.

Texas↗

USGS1980

Intrusions and intrusive complexes in an ophiolite near San Luis Obispo; a chemical and petrologic study

The San Luis Obispo ophiolite is a sequence of mafic and ultramafic rocks that lie as a thrust-like slice on top of Franciscan melange in the southern California Coast Range. The ophiolite comprises the classic Steinmann Trinity of basal serpentinized ultramafic rocks overlain sequentially by spilitized pillow lavas and cherts. The ophiolite is intruded by numerous diabasic dikes and several large intrusive complexes that contain peridotite, gabbro, diabase and felsic rocks. Field relations indicate that this ophiolite originated as a sequence of submarine volcanic flows and breccia units extruded onto an ultramafic basement. Later the volcanic and ultramafic rocks were intruded along their contact by mafic magma that crystallized as a stratiform complex of cumulate peridotite and gabbro. Next, this stratiform complex was intruded by diorite and albite-granite (trondhjemite) sills, which may have been produced by partial melting of gabbros in the upper levels of the stratiform complex. Finally all earlier units were intruded by diabasic sills and dikes that probably were late feeders for the pre-existing volcanic unit. All the ophiolite rocks underwent subsequent highly localized brecciation, under greenschist-facies conditions, in which felsic rocks were incipiently melted by frictional heating. The host rocks and intrusions were metamorphosed at low temperature and the mafic rocks were altered by Na- and Si-metasomatism. Despite this pervasive alteration, evidences of the formational stages of the ophiolite are preserved in disequilibrium mineral assemblages, primarily within mafic and ultramafic rocks of the intrusive complexes. Whole-rock analyses of the ophiolite suite indicate that alteration has obscured but not obliterated the original chemical character of the mafic rocks. The ophiolite diabases and basalts contain up to 6 weight percent Na 2 0 and 58 percent Si0 2 , in contrast to normal Si0 2 contents of 50 percent or less and Na 2 0 contents of less than 3 percent for unaltered oceanic and continental tholeiite basalts. However, the low K 2 0 contents (less than 0.8 percent) of all units in the ophiolite suite indicate that these rocks are not part of an alkalic kindred, but rather are altered tholeiites. Compositions of relict amphibole and plagioclase in the mafic rocks indicate that the ophiolite formed in a high-temperature environment and the deep seated rocks were metamorphosed under amphibolite-facies conditions. A later change in the environmental conditions allowed subsequent low-temperature (greenschist facies) metamorphism and metasomatism. The structure and chemistry of the San Luis Obispo ophiolite support the hypothesis that this body may represent a fragment of oceanic crust and mantle. The volcanic rocks and the intrusive complexes probably formed at a mid-ocean ridge, where conditions of high heat-flow provided the requisite high-temperature environment and promoted the production of mafic magmas. The change to low-temperature conditions probably was due to inception or acceleration of crustal spreading at that portion of the ridge where this ophiolite formed. The nature of brecciation in the ophiolite indicates that the low-temperature environment also was one of greater tectonic disturbance, relative to conditions at the ridge. This tectonically active environment probably corresponds to an island arc where the ophiolite-bearing plate was subducted in an adjacent trench. The absence of a high-pressure mineral assemblage in the San Luis Obispo ophiolite suggests that this segment of ocean-crust and upper mantle was not buried in a subduction zone, but rather was rafted on top of subduction melange (Franciscan Formation) into its present position.

California↗

USGS1990

Hydrology and land use in Grand Traverse County, Michigan

Glacial deposits are the sole source of ground-water supplies in Grand Traverse County. These deposits range in thickness from 100 to 900 feet and consist of till, outwash, and materials of lacustrine and eolian origin. In some areas, the deposits fill buried valleys that are 500 feet deep. Sedimentary rocks of Paleozoic age, which underlie the glacial deposits, are mostly shale and are not used for water supply. Of the glacial deposits, outwash and lacustrine sand are the most productive aquifers. Most domestic wells obtain water from sand and gravel at depths ranging from 50 to 150 feet and yield at least 20 gallons per minute. Irrigation, municipal, and industrial wells capable of yielding 250 gallons per minute or more are generally greater than 150 feet deep. At places in the county where moranial deposits contain large amounts of interbedded silt and clay, wells are generally deeper and yields are much lower. Areal variations in the chemical and physical characteristics of ground and surface water are related to land use and chemical inputs to the hydrologic system. Information on fertilizer application, septic-tank discharges, animal wastes, and precipitation indicate that 40 percent of nitrogen input is from precipitation, 6 percent from septic tanks, 14 percent from animal wastes, and 40 percent from fertilizers. Streams and lakes generally have a calcium bicarbonate-type water. The dissolved-solids concentration of streams ranged from 116 to 380 milligrams per liter, and that of lakes, from 47 to 170 milligrams per liter. Water of streams is hard to very hard; water of lakes ranges from soft to hard. The maximum total nitrogen concentration found in streams was 4.4 milligrams per liter. Water of lakes have low nitrogen concentrations; the median nitrate concentration is less than 0.01 milligrams per liter. Pesticides (Parathion and Simazine) were detected in low concentrations at six stream sites; 2,4-D was detected in low concentrations in water of two lakes. Relationships between land use and the yield of dissolved and suspended substances could not be established for most stream basins. Calcium and bicarbonate are the principal dissolved substances in ground water. Dissolved-solids concentrations ranged from 70 to 700 milligrams per liter; the countywide mean concentration is 230 milligrams per liter. The mean nitrate concentration is 1.3 milligrams per liter; about 1.6 percent of the county's ground water has nitrate concentrations that exceed the U.S. Environmental Protection Agency's maximum drinking water level of 10 milligrams per liter. An effect of fertilizer applications on ground-water quality is evident in some parts of the county.

Michigan↗

USGS2002

Preliminary geophysical characterization of two oil production sites, Osage County, Oklahoma - Osage Skiatook Petroleum Environmental Research Project

Ground electromagnetic and dc resistivity geophysical surveys were used to interpret the subsurface distribution of salinized soil, water, and bedrock at two sites (A and B) and to characterize the larger scale hydrologic setting. Measurements were made on grids of about 1000 square meters using a very shallow penetrating (less than 10 m) electromagnetic (EM) geophysical system (EM31). At site A, high subsurface conductivities (more than 100 millisiemens per meter) found below disposal ponds extended down the local hydrologic gradient to below the normal level of near by Lake Skiatook. At site B, areas of highest subsurface electrical conductivity were offset about 10 m from the center of salt scars. The area of high subsurface electrical conductivity extends in the subsurface below the normal level of Skiatook Lake. DC resistivity soundings were made in and around the two sites in order to characterize deeper (30-60 m) electrical properties of the subsurface lithology and ground water. These soundings indicate that the tight shale that dominates the local lithology is moderately electrically conductive (5 milliseimems per meter). DC soundings done in several areas at the Skiatook Lake shoreline indicate an electrically conductive (less than 10 millisiemens per meter) zone exists below the shore even away from the oil production sites. This conductive zone may indicate a mixing between fresh lake water and local ground water that has high dissolved solids. Borehole geophysical logs at site B and laboratory rock property measurements are currently being used to refine interpretation of ground geophysical measurements.

Oklahoma↗

USGS2004

Selenium loading through the Blackfoot River watershed--linking sources to ecosystem

The upper Blackfoot River watershed in southeast Idaho receives drainage from 11 of 16 phosphate mines that have extracted ore from the Phosphoria Formation, three of which are presently active. Toxic effects from selenium (Se), including death of livestock and deformity in aquatic birds, were documented locally in areas where phosphatic shales are exposed ( Piper et al., 2000 ; Presser et al., Chapter 11). Current drainage conditions are leading to Se bioaccumulation at concentrations that pose a risk to fish in the Blackfoot River and its tributaries (Hamilton et al., Chapter 18). A gaging station on the Blackfoot River was re-activated in April 2001 to assess hydrologic conditions and concentration, load, and speciation for Se discharges on a watershed scale. The gaging-station data are considered to represent regional drainage conditions in the upper Blackfoot River water- shed because of its location near the outlet of the watershed and directly upstream of the Blackfoot Reservoir. Watershed discharges for 2001 and 2002 were below minimum hydrologic conditions for the gage as documented by the historical record. Drought emergencies were declared in the area in both 2001 and 2002. Unmonitored diversions for irrigation that routinely take place during the snowmelt season also affected conditions downstream. Annual cycles in Se concentration, load, and selenate (Se 6+ ) reached maxima in the spring during the period of maximum flow at the gaging station. Thirty-seven to 44% of annual flow occurred dur- ing the three-month high-flow season (April through June) in 2001 and 56% of annual flow occurred during that time period in 2002. Extrapolation from historical hydrographs for average and wet years and a limited data set of regional Se concentrations for 2001 and 2002 indicated potential for a 3.6- to 7.4-fold increase in Se loading because of increased seasonal flows in the Blackfoot River watershed. Supplementation data indicate that: (a) the difference between total Se and dissolved Se, as a measure of the contribution of particulate Se, was < 10% except at the peak of con- centration when total Se was 18% more than dissolved Se; (b) selenite (Se 4+ ) represented less than 10% of the dissolved species during all months of 2001; and (c) dissolved Se was approximately a 50:50 mixture of selenate and organic selenide (operationally defined Se 2- ) during summer 2001 (June through August). Ecological risk based on regional Se drainage occurred during both the high- and low-flow seasons. Seventy to 83% of the Se load occurred during the high-flow season. During early May of both years, dissolved-Se concentrations exceeded the criterion for the protection of aquatic life and the ecological threshold of 5 gL 1 Se at which sub- stantive risk occurs. During the majority of the three-month high-flow season, dissolved- Se concentrations exceeded the 2 gL 1 Se concern level for aquatic biota. The Se concentration in suspended material during high flow in 2002 was within the range of marginal risk to aquatic life (2-4 gg 1 Se, dry weight). Selenate was the major species during peak flows, with both selenate and organic selenide being major species during relatively low-flow periods in summer. A change in speciation to reduced Se may indicate elevated biotic productivity during summer months and could result in enhanced Se uptake in food webs. In addition to the magnitude of regional Se release in the Blackfoot River watershed, Se concentrations in individual source drains and waste-rock seeps, and those predicted by experimental column leaching of proposed mining overburden materials, also indicate that drainage options that currently meet existing demands for phosphate mining cause eco- logical risk thresholds to be exceeded. At times, the drinking-water Se standard (50 g L 1 Se) and the criterion for hazardous Se waste (1000 L -1 Se) ( US Department of the Interior, 1998 ; US Environmental Protection Agency, 1987 ) are also exceeded. For water-years 2001 and 2002, seasonal increased input of water in the mining area resulted in increased Se transport, suggesting a mechanism of contamination that involves a significant Se reservoir. Hence, recognition and monitoring of Se loading to the envi- ronment on a mass balance basis (i.e. inputs, fluxes and storage within environmental media, and outputs) are essential to evaluating how to control Se concentrations within environmentally protective ranges ( Presser and Piper, 1998 ). In areas where release of Se to aquatic systems is anticipated as a product of future expansion of phosphate mining, continuous monitoring of flow and development of seasonal Se loading patterns would help to model watersheds in terms of sources, flow periods, and environmental-Se con- centrations that most influence bioavailability. These data, in turn, could be linked to Se- bioaccumulation models specific to food webs and vulnerable species of the impacted areas to accurately project ecological effects. Gaging at this site on the Blackfoot River is planned to continue in order to establish a long-term (>10 year) record of hydrologic conditions.

Idaho↗