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At least 1,261 records · Page 70Linked to original sources
USGS1996

The nature, distribution, and origin of gas hydrate in the Chile Triple Junction region

A bottom simulating reflector (BSR) is regionally distributed throughout much of the Chile Triple Junction (CTJ) region. Downhole temperature and logging data collected during Ocean Drilling Program (ODP) Leg 141 suggest that the seismic BSR is generated by low seismic velocities associated with the presence of a few percent free gas in a ??? 10 m thick zone just beneath the hydrate-bearing zone. The data also indicate that the temperature and pressure at the BSR best corresponds to the seawater/methane hydrate stability field. The origin of the large amounts of methane required to generate the hydrates is, however, problematic. Low total organic carbon contents and low alkalinities argue against significant in situ biogenic methanogenesis, but additional input from thermogenic sources also appears to be precluded. Increasing thermal gradients, associated with the approach of the spreading ridge system, may have caused the base of the hydrate stability field to migrate 300 m upwards in the sediments. We propose that the upward migration of the base of the stability field has concentrated originally widely dispersed hydrate patches into the more continuous hydrate body we see today. The methane can be concentrated if the gas hydrates can form from dissolved methane, transported into the hydrate zone via diffusion or fluid advection. A strong gradient may exist in dissolved methane concentration across the BSR leading to the steady reabsorbtion of the free gas zone during the upward migration of the BSR even in the absence of fluid advection.

Earth and Planetary Science Letters↗
USGS1958

Retention of lead during oxidative ashing of selected naturally occurring carbonaceous substances

The amount of lead retained in the ash of lead-bearing carbonaceous material is essentially independent of the method of ashing. Samples containing lead in the range of 0.00X to 0.X per cent were ashed by ignition in a high-oxygen atmosphere and were also wet-ashed. The lead in the ash was determined colorimetrically. Results were the same by both methods, but the time required is 3 to 10 times less for the dry-ashing method.

Geochimica et Cosmochimica Acta↗
USGS1958

Some natural variations in the relative abundance of copper isotopes

The relative isotopic abundance of copper has been measured in a number of minerals and a few plant materials. Suites of samples from Michigan and the Colorado Plateau have been examined in more detail to determine if local variations due to isotopic exchange or diffusion could be found. The relative isotopic abundance of copper in specimens from several other localities was also determined. The variations noted were small but in some cases were felt to be significant because they were larger than the experimental error (0·1 per cent in the ratio). A total spread of −1 to +8 parts per mil compared to the standard was found in the specimens tested.

Geochimica et Cosmochimica Acta↗
USGS1983

The contribution of humic substances to the acidity of colored natural waters

An operationally defined carboxyl content of humic substances extracted from rivers, streams, lakes, wetlands, and groundwaters throughout the United States and Canada is reported. Despite the diversity of the samples, only small variations were observed in this humic carboxyl content. The dissociation behavior of two combined fulvic/humic acid extracts was studied and it was found that the dissociation of the humics varied in a predictable manner with pH. Using a carboxyl content of 10 μeq/ mg humic organic carbon, and mass action quotient calculated from sample pH, the ionic balances of three highly colored Nova Scotia rivers were estimated.

Geochimica et Cosmochimica Acta↗
USGS1993

Thermal stability of hydrocarbons in nature: Limits, evidence, characteristics, and possible controls

Numerous petroleum-geochemical analyses of deeply buried, high-rank, fine-grained rocks from ultra-deep wellbores by different investigators demonstrate that C 15 + hydrocarbons (HCs) persist in moderate to high concentrations at vitrinite reflectance ( R 0 ) values of 2.0–5.0% and persist in measurable concentrations up to R 0 = 7.0–8.0%, at which point the thermal deadline for C 15 + HC's is finally approached. Qualitative analyses have been carried out on 1. (1) high-rank gas condensates which have been exposed to the HC-thermal-destructive phase, 2. (2) bitumens from high-temperature aqueous-pyrolysis experiments in the HC-thermal-destructive phase, and 3. (3) bitumens from high-rank, fine-grained rocks near the HC-thermal-destructive phase. These analyses clearly demonstrate that well-defined compositional suites are established in the saturated, aromatic, and sulfur-bearing aromatic HCs in and near the HC-thermal-destructive phase. On the other hand, accepted petroleum-geochemical paradigms place rigid limits on HC thermal stability: C 15 + HCs begin thermal cracking at R 0 values of 0.9% and are completely thermally destroyed by R 0 = 1.35%; C 2 -C 4 HC gases are thermally destroyed by R 0 = 2.0% and methane is thermally destroyed by R 0 = 4.0%. Furthermore, published data and observations in many HC basins worldwide support these models; for example, 1. (1) sharp basinal zonations of gas and oil deposits vs. maturation rank in HC basins and 2. (2) decreasing C 15 + HC concentrations in some fine-grained rocks at ranks of R 0 ≥ 0.9%. The fact that observed data (C 15 + HCs thermally stable to R 0 = 7.0–8.0%) is so far removed from predicted behavior (C 15 + ) HCs expected to be thermally destroyed by R 0 = 1.35%) may be due to 1. (1) a lack of recognition of some important possible controlling parameters of organic matter (OM) metamorphism and too much importance given to other assumed controlling parameters; and 2. (2) assigning HC distribution patterns in petroleum basins to HC thermal cracking when such patterns may be due to other causes. In the first case, laboratory experiments strongly suggest that the presence of water, increasing fluid pressures, and closed systems (product retention) all suppress OM metamorphic reactions. Conversely, the absence of water, low fluid pressures, and open systems (product escape) all promote OM metamorphic reactions. These experiments also demonstrate that OM metamorphic reactions proceed by reaction kinetics greater than first order. Thus, the effect of geologic time appears to have been over-estimated in OM metamorphism. In the second case, the strong decreases in C 15 + HC concentrations in fine-grained rocks with Type III OM over R 0 = 0.9−1.35% are most probably due to intense primary migration and loss of HCs to drilling muds during the trip uphole in drilling operations. Data from coals demonstrate that these decreases in HC concentrations cannot be due to C 15 + HC thermal destruction. Oil deposits are generally found at shallow depths in basins, and “dry gas” (methane ≤ 98% of all HC gases) deposits are found at the greatest depths. This HC distribution pattern would be caused by methane, generated during the late stages of C 15 + HC generation, flushing oil (including C 2 –C 4 HC gases condensed into the liquid phase) out of deep basinal traps by Gussow's (1954) principle of differential entrapment. Hence, only “dry gas” deposits are left in the basin deeps. Oil emplacement processes in traps during expulsion and secondary migration could also contribute to the HC distribution pattern observed in petroleum basins.

Geochimica et Cosmochimica Acta↗
USGS1965

Natural recharge and localization of fresh ground water in Kuwait

Fresh ground water (200 parts per million total dissolved solids and upwards) occurs in portions of Pleistocene sandstone aquifers beneath basins and wadis in north Kuwait where the mean rainfall is about five inches per year. The fresh water is surrounded and underlain by brackish water (> 4000 ppm TDS). Drilling and testing show that fresh water saturation is restricted to wadis and basin areas; in Rawdatain basin it attains a maximum thickness of about 110 feet and a lateral extent of about seven miles. The fresh ground water represents recharge localized, during infrequent, torrential rain storms, in areas of concentrated runoff where sediments in the vadose zone are moderately permeable and depth to the water table is generally less than a hundred feet. Concentration of runoff appears to be the primary control in the localization of recharge. The fresh water percolates downward to the ground-water reservoir following rare storms, then flows in the direction of hydraulic gradient and gradually becomes brackish. Theoretical delineation of the recharge area and ground-water flow pattern in Rawdatain was confirmed by tritium and C 14 dating of the water. Brackish ground-water conditions prevail from water table downward in areas where rainfall infiltrates essentially where it falls, permeability of sediments in the vadose zone is low, or the water table is several hundred feet below land surface. In these areas, rainfall is retained and lost within the soil zone or becomes mineralized during deep percolation.

Journal of Hydrology↗
USGS1982

Natural groundwater recharge in an upland area of central North Dakota, U.S.A.

The magnitude of groundwater recharge to coal aquifers in a 150-km 2 area in west-central North Dakota was determined using three separate approaches: (1) the net water level rise in water-table wells; (2) calculations of the fluid flux between nested piezometers, using the Darcy equation and measured values of hydraulic conductivity and vertical gradients; and (3) evaluation of the inputs to and outputs from the coal aquifer, using a steady-state control volume approach in which the aquifer was divided into semi-rectangular cells bounded by equipotential lines and flow lines. Measurements of potential gradients and hydraulic conductivity permitted indirect determination of all components of flow into and out of the cell except the recharge input, which was determined by difference. All methods yielded consistent results on the order of 0.04-0.01 m yr. −1 These values, which represent 2–9% of the annual precipitation, are consistent with results of other studies on recharge throughout the prairies of North America. Evaluation of site hydrology and stable-isotope data indicates that recharge is restricted in both time and place. Most recharge occurs in late spring and in the fall following heavy rainfall events. During these seasons the ground is not frozen and vegetation is not transpiring large amounts of water. Some recharge may occur during very heavy localized summer storms, but it is not considered volumetrically significant. Major permanent depressions on the site are a source of significant recharge. In addition, the extensive area of ephemeral standing water bodies that result from snowmelt can produce significant amounts of infiltration over the entire site.

central North Dakota↗
USGS1969

Beach lamination: Nature and origin

A distinctive two-fold sedimentation unit characterizes lamination in the upper swash zone of beaches. Within the unit a fine and/or a heavy mineral rich layer at the base grades upward into a coarser and/or a heavy mineral poor layer at the top. This distinctive type of lamination results from grain segregation within bed flow during wave backwash.

Marine Geology↗
USGS1984

Geochemistry of a naturally occurring massive marine gas hydrate

During Deep Sea Drilling Project (DSDP) Leg 84 a core 1 m long and 6 cm in diameter of massive gas hydrate was unexpectedly recovered at Site 570 in upper slope sediment of the Middle America Trench offshore of Guatemala. This core contained only 5–7% sediment, the remainder being the solid hydrate composed of gas and water. Samples of the gas hydrate were decomposed under controlled conditions in a closed container maintained at 4°C. Gas pressure increased and asymptotically approached the equilibrium decomposition pressure for an ideal methane hydrate, CH 4 .5-3/4H 2 O, of 3930 kPa and approached to this pressure after each time gas was released, until the gas hydrate was completely decomposed. The gas evolved during hydrate decomposition was 99.4% methane, ∼0.2% ethane, and ∼0.4% CO 2 . Hydrocarbons from propane to heptane were also present, but in concentrations of less than 100 p.p.m. The carbon-isotopic composition of methane was −41 to −44 permil(( 0 00 "> 000 ), relative to PDB standard. The observed volumetric methane/water ratio was 64 or 67, which indicates that before it was stored and analyzed, the gas hydrate probably had lost methane. The sample material used in the experiments was likely a mixture of methane hydrate and water ice. Formation of this massive gas hydrate probably involved the following processes: (i) upward migration of gas and its accumulation in a zone where conditions favored the growth of gas hydrates, (ii) continued, unusually rapid biological generation of methane, and (iii) release of gas from water solution as pressure decreased due to sea level lowering and tectonic uplift.

Middle America Trench↗
USGS1993

Interaction of rising frazil with suspended particles: Tank experiments with applications to nature

Widespread occurrence of sediment-laden (turbid) sea ice and high concentrations of diatoms and foraminifers in ice have recently been reported from both polar regions. Many possible mechanisms of particle entrainment into ice have been postulated, among which scavenging by rising frazil ice and nucleation or adhesion of ice onto suspended particles appear to be the most likely ones. No reliable experimental data on the mechanisms, however, are available. Because of the importance of turbid ice for sediment transport, tanks for laboratory-scale experiments were constructed, in which frazil crystals produced at the base were monitored rising through water column laden with various types of particulate matter, including plankton. Observations made in salt water are reported here. Over a distance of 1.5 m, frazil < 1 mm in diameter grew to crystals or flocs several cm in diameter, rising at average velocities of 2 to 3 cm/s. Rise velocities were a function of frazil size, but varied greatly due to interactions of ice particles of different size and velocity and the resulting turbulence. Sand-size particles could be either trapped permanently by rising frazil, or were temporarily supported and again released. With live plankton, a several-fold enrichment of ice occurred, suggesting that their irregular shapes or appendages were caught by ice flocs. Diatom- and foram tests were also relatively effectively trapped. The concentration of silt- and clay-size terrigenous detritus in frazil tended to increase relative to the water. We found no preferential sorting by ice in this size range. Various kinds of evidence showed that ice does not nucleate onto foreign particles, and has no adhesive properties. Foreign material resided in the interstices of crystal aggregates, and particles denser than water could be released by agitation, suggesting that scavenging is a mechanical process. With rising frazil, the settling of particulate matter therefore is either retarded or reversed, resulting in a net upward sediment flux and a sediment-laden ice cover from this process of suspension freezing.

Cold Regions Science and Technology↗
USGS1978

The geochemical nature of the Archean Ancient Gneiss Complex and Granodiorite Suite, Swaziland: A preliminary study

The Ancient Gneiss Complex (AGC) of Swaziland, an Archean gray gneiss complex, lies southeast and south of the Barberton greenstone belt and includes the most structurally complex and highly metamorphosed portions of the eastern Kaapvaal craton. The AGC is not precisely dated but apparently is older than 3.4 Ga. The AGC consists of three major units: (a) a bimodal suite of closely interlayered siliceous, low-K gneisses and metabasalt; (b) homogeneous tonalite gneiss; and (c) interlayered siliceous microcline gneiss, metabasalt, and minor metasedimentary rocks - termed the metamorphite suite. A geologically younger gabbro-diorite-tonalite-trondhjemite suite, the Granodiorite Suite, is spatially associated with the AGC and intrusive into it. The bimodal suite consists largely of two types of low-K siliceous gneiss: one has SiO 2 < 75%, Al 2 O 3 > 14%, low Rb/Sr ratios, and depleted heavy rare earth elements (REE's); the other has SiO 2 > 75%, Al 2 O 3 < 13%, high Rb/Sr ratios, and relatively abundant REE's except for negative Eu anomalies. The interlayered metabasalt ranges from komatiitic to tholeiitic compositions. Lenses of quartz monzonitic gneiss of K 2 O/Na 2 O close to 1 form a minor part of the bimodal suite. Tonalitic to trondhjemitic migmatite locally is abundant and has major-element abundances similar to those of non-migmatitic varieties. The siliceous gneisses of the metamorphic suite show low Al 2 O, K 2 O/Na 2 O ratios of about 1, high Rb/Sr ratios, moderate REE abundances and negative Eu anomalies. K/Rb ratios of siliceous gneisses of the bimodal suite are very low (∼130); of the tonalitic gneiss, low (∼225); of the siliceous gneiss of the metamorphite suite, moderate (∼300); and of the Granodiorite Suite, high (∼400). Rocks of the AGC differ geochemically in several ways from the siliceous volcanic and hypabyssal rocks of the Upper Onverwacht Group and from the diapirs of tonalite and trondhjemite that intrude the Swaziland Group.

Precambrian Research↗
USGS1992

The nature of Archean terrane boundaries: An example from the northern Wyoming Province

The Archean northern Wyoming Province can be subdivided into two geologically distinct terranes, the Beartooth-Bighorn magmatic terrane (BBMT) and the Montana metasedimentary terrane (MMT). The BBMT is characterized by voluminous Late Archean (2.90-2.74 Ga) magmatic rocks (primarily tonalite, trondhjemite, and granite); metasedimentary rocks are preserved only as small, rare enclaves in this magmatic terrane. The magmatic rocks typically have geochemical and isotopic signatures that suggest petrogenesis in a continental magmatic arc environment. The MMT, as exposed in the northern Gallatin and Madison Ranges, is dominated by Middle Archean trondhjemitic gneisses (3.2-3.0 Ga); metasedimentary rocks, however, are significantly more abundant than in the BBMT. Each terrane has experienced a separate and distinct geologic history since at least 3.6 Ga ago based on differences in metamorphic and structural styles, composition of magmatic and metasupracrustal rocks, and isotopic ages; consequently, these may be described as discrete terranes in the Cordilleran sense. Nonetheless, highly radiogenic and distinctive Pb-Pb isotopic signatures in rocks of all ages in both terranes indicate that the two terranes share a significant aspect of their history. This suggests that these two Early to Middle Archean crustal blocks, that initially evolved as part of a larger crustal province, experienced different geologic histories from at least 3.6 Ga until their juxtaposition in the Late Archean (between 2.75 to 2.55 Ga ago). Consequently, the boundary between the BBMT and MMT appears to separate terranes that are not likely to be exotic in the sense of their Phanerozoic counterparts. Other Archean provinces do appear to contain crustal blocks with different isotopic signatures (e.g. West Greenland, India, South Africa). The use of the term exotic, therefore, must be cautious in situations where geographic indicators such as paleontologic and/or paleomagnetic data are not available. In these cases, isotopic signatures are one of the most useful features for assessing overall genetic relations amongst geologically distinct terranes.

Idaho, Montana, Wyoming↗
USGS1983

The nature of carbon dioxide waters in Snaefellsnes, western Iceland

Over 20 occurrences of thermal and non-thermal waters rich in carbon dioxide are known in the Snaefellsnes Peninsula of western Iceland. On the basis of the thermal, chemical and isotopic characteristics of these waters, and hydrological considerations, it is concluded that they represent meteoric waters which have seeped to variable depths into the bedrock. Ascending carbon dioxide gas originating from intrusions or the mantle mixes with the meteoric waters to produce carbon dioxide waters: at considerable depth in the case of the thermal carbon dioxide waters but close to the surface in the case of cold carbon dioxide waters. The occurrence of carbon dioxide waters cannot be regarded as evidence for underground geothermal reservoirs.

Geothermics↗
USGS1993

Surface chemical effects on colloid stability and transport through natural porous media

Surface chemical effects on colloidal stability and transport through porous media were investigated using laboratory column techniques. Approximately 100 nm diameter, spherical, iron oxide particles were synthesized as the mobile colloidal phase. The column packing material was retrieved from a sand and gravel aquifer on Cape Cod, MA. Previous studies have indicated enhanced stability and transport of iron oxide particles due to specific adsorption of some inorganic anions on the iron oxide surface. This phenomenon was further evaluated with an anionic surfactant, sodium dodecyl sulfate. Surfactants constitute a significant mass of the contaminant loading at the Cape Cod site and their presence may contribute to colloidal transport as a significant transport mechanism at the site. Other studies at the site have previously demonstrated the occurrence of this transport mechanism for iron phosphate particles. Photon correlation spectroscopy, micro-electrophoretic mobility, and scanning electron microscopy were used to evaluate particle stability, mobility and size. Adsorption of negatively charged organic and inorganic species onto the surface of the iron oxide particles was shown to significantly enhance particle stability and transport through alterations of the electrokinetic properties of the particle surface. Particle breakthrough generally occurred simultaneously with tritiated water, a conservative tracer. The extent of particle breakthrough was primarily dependent upon colloidal stability and surface charge.

Massachusetts↗
USGS2006

Stability of low levels of perchlorate in drinking water and natural water samples

Perchlorate ion (ClO4-) is an environmental contaminant of growing concern due to its potential human health effects, impact on aquatic and land animals, and widespread occurrence throughout the United States. The determination of perchlorate cannot normally be carried out in the field. As such, water samples for perchlorate analysis are often shipped to a central laboratory, where they may be stored for a significant period before analysis. The stability of perchlorate ion in various types of commonly encountered water samples has not been generally examined-the effect of such storage is thus not known. In the present study, the long-term stability of perchlorate ion in deionized water, tap water, ground water, and surface water was examined. Sample sets containing approximately 1000, 100, 1.0, and 0.5 ??g l-1 perchlorate ion in deionized water and also in local tap water were formulated. These samples were analyzed by ion chromatography for perchlorate ion concentration against freshly prepared standards every 24 h for the first 7 days, biweekly for the next 4 weeks, and periodically after that for a total of 400 or 610 days for the two lowest concentrations and a total of 428 or 638 days for the high concentrations. Ground and surface water samples containing perchlorate were collected, held and analyzed for perchlorate concentration periodically over at least 360 days. All samples except for the surface water samples were found to be stable for the duration of the study, allowing for holding times of at least 300 days for ground water samples and at least 90 days for surface water samples. ?? 2006 Elsevier B.V. All rights reserved.

Analytica Chimica Acta↗