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J. B. Rapp

Publications and source records attributed to J. B. Rapp.

16 recordsLinked to original sources
USGS2012

Geochemistry of some gases in hydrothermal fluids from the southern Juan de Fuca Ridge

Five samples of hydrothermal fluids from two vent areas on the southern Juan de Fuca Ridge were analyzed for dissolved gases. Concentrations in the end-member hydrothermal fluid of H 2 (270–527 μmol/kg), CH 4 (82–118 μmol/kg), and CO 2 (3920–4460 μmol/kg) are well above values in ambient seawater and are similar to concentrations reported for other ridge crest hydrothermal systems. The carbon isotopic ratios of the CH 4 (δ 13 C = −17.8 to −20.8) and CO 2 (δ 13 C = −3.6 to −4.7) suggest that at least some of the CH 4 and CO 2 in the fluids is basalt-derived. The range of δ 13 C values for the basalt-derived CO 2 is −6.8 to −9.7, calculated by assuming conservation of recharge ΣCO 2 during hydrothermal circulation. Apparent temperatures of equilibration between the CH 4 and the basalt-derived CO 2 range from 640°C to 750°C. Small amounts of ethane (C 2 H 6 /CH 4 ≅ 0.9 × 10 −3 −2.2 × 10 −3 ), propane, and butane detected in the samples may also have formed in the basalt. One sample of almost pure (95.5%) hydrothermal fluid contained a significant fraction, up to 63% and 74%, respectively, of the recharge Ar and N 2 . This suggests that the fluid has not undergone extensive vapor-liquid phase separation.

Journal of Geophysical Research Solid Earth↗
USGS2002

Ubiquitous tar balls with a California-source signature on the shorelines of Prince William Sound, Alaska

Although the shorelines of Prince William Sound still bear traces of the 1989 Exxon Valdez oil spill, most of the flattened tar balls that can be found today on these shorelines are not residues of Exxon Valdez oil. Instead, the carbon-isotopic and hydrocarbonbiomarker signatures of 61 tar ball samples, collected from shorelines throughout the northern and western parts of the sound, are all remarkably similar and have characteristics consistent with those of oil products that originated from the Monterey Formation source rocks of California. The carbonisotopic compositions of the tar balls are all closely grouped (<513Cpdb = -23.7 ± 0.2%o), within the range found in crude oils from those rocks, but are distinct from isotopic compositions of 28 samples of residues from the Exxon ValdezoW spill (<513Cpdb = -29.4 ± 0.1%o). Likewise, values for selected biomarker ratios in the tar balls are all similar but distinct from values of residues from the 1989 oil spill. Carbon-isotopic and biomarker signatures generally relate the tar balls to oil products used in Alaska before ~1970 for construction and pavements. How these tar balls with such similar geochemical characteristics became so widely dispersed throughout the northern and western parts of the sound is not known with certainty, but the great 1964 Alaska earthquake was undoubtedly an important trigger, causing spills from ruptured storage facilities of California-sourced asphalt and fuel oil into Prince William Sound.

Alaska↗
USGS1996

Distributions and fate of chlorinated pesticides, biomarkers and polycyclic aromatic hydrocarbons in sediments along a contamination gradient from a point-source in San Francisco Bay, California

The distribution and fate of chlorinated pesticides, biomarkers, and polycyclic aromatic hydrocarbons (PAHs) in surficial sediments along a contamination gradient in the Lauritzen Canal and Richmond Harbor in San Francisco Bay was investigated. Compounds were identified and quantified using gas chromatography-ion trap mass spectrometry. Biomarkers and PAHs were derived primarily from weathered petroleum. DDT was reductively dechlorinated under anoxic conditions to DDD and several minor degradation products, DDMU, DDMS, and DDNU. Under aerobic conditions, DDT was dehydrochlorinated to DDE and DBP. Aerobic degradation of DDT was diminished or inhibited in zones of high concentration, and increased significantly in zones of lower concentration: Other chlorinated pesticides identified in sediment included dieldrin and chlordane isomers. Multivariate analysis of the distributions of the DDTs suggested that there are probably two sources of DDD. In addition, DDE and DDMU are probably formed by similar mechanisms, i.e. dehydrochlorination. A steep concentration gradient existed from the Canal to the Outer Richmond Harbor, but higher levels of DDD than those found in the remainder of the Bay indicated that these contaminants are transported on particulates and colloidal organic matter from this source into San Francisco Bay. Chlorinated pesticides and PAHs may pose a potential problem to biota in San Francisco Bay.

Marine Environmental Research↗
USGS1996

Occurrence and accumulation of pesticides and organic contaminants in river sediment, water and clam tissues from the San Joaquin River and tributaries, California

A study was conducted in 1992 to assess the effects of anthropogenic activities and land use on the water quality of the San Joaquin River and its major tributaries. This study focused on pesticides and organic contaminants, looking at distributions of contaminants in water, bed and suspended sediment, and the bivalve Corbicula fluminea. Results indicated that this river system is affected by agricultural practices and urban runoff. Sediments from Dry Creek contained elevated concentrations of polycyclic aromatic hydrocarbons (PAHs), possibly derived from urban runoff from the city of Modesto; suspended sediments contained elevated amounts of chlordane. Trace levels of triazine herbicides atrazine and simazine were present in water at most sites. Sediments, water, and bivalves from Orestimba Creek, a westside tributary draining agricultural areas, contained the greatest levels of DDT (1,1,1-trichloro-2-2-bis[p-chlorophenyl]ethane), and its degradates DDD (1,1-dichloro-2,2-bis[p-chlorophenyl]ethane), and DDE (1,1-dichloro-2,2- bis[p-chlorophenyl]ethylene). Sediment adsorption co efficients (K(oc)), and bioconcentration factors (BCF) in Corbicula of DDT, DDD, and DDE at Orestimba Creek were greater than predicted values. Streams of the western San Joaquin Valley can potentially transport significant amounts of chlorinated pesticides to the San Joaquin River, the delta, and San Francisco Bay. Organochlorine compounds accumulate in bivalves and sediment and may pose a problem to other biotic species in this watershed.

California↗
USGS1993

Hydrocarbons in oil residues on beaches of islands of Prince William Sound, Alaska

Aliphatic and aromatic hydrocarbons were measured on oil residues from beaches on six islands in Prince William Sound, Alaska. In addition to altered products from the Exxon Valdez oil spill of 1989, we also found, at two widely separated locations, residues that are similar to each other but chemically distinct from the spilled oil. Terpanes, steranes, monoaromatic steranes, and carbon isotopic compositions of total extracts were most useful in correlating the altered products of the spilled oil. These same parameters revealed that the two non-Valdez samples are likely residues of oil originally produced in California. The results indicate that oil residues currently on the beaches of this estuary have at least two quite different origins.

Marine Pollution Bulletin↗
USGS1991

A statistical approach to the interpretation of aliphatic hydrocarbon distributions in marine sediments

Q-mode factor analysis was used to quantitate the distribution of the major aliphatic hydrocarbon (n-alkanes, pristane, phytane) systems in sediments from a variety of marine environments. The compositions of the pure end members of the systems were obtained from factor scores and the distribution of the systems within each sample was obtained from factor loadings. All the data, from the diverse environments sampled (estuarine (San Francisco Bay), fresh-water (San Francisco Peninsula), polar-marine (Antarctica) and geothermal-marine (Gorda Ridge) sediments), were reduced to three major systems: a terrestrial system (mostly high molecular weight aliphatics with odd-numbered-carbon predominance), a mature system (mostly low molecular weight aliphatics without predominance) and a system containing mostly high molecular weight aliphatics with even-numbered-carbon predominance. With this statistical approach, it is possible to assign the percentage contribution from various sources to the observed distribution of aliphatic hydrocarbons in each sediment sample. ?? 1991.

Chemical Geology↗
USGS1989

Organic markers as source discriminants and sediment transport indicators in south San Francisco Bay, California

Sediment samples from nearshore sites in south San Francisco Bay and from streams flowing into that section of the Bay have been characterized in terms of their content of biogenic and anthropogenic molecular marker compounds. The distributions, input sources, and applicability of these compounds in determining sediment movement are discussed. By means of inspection and multivariate analysis, the compounds were grouped according to probable input sources and the sampling stations according to the relative importance of source contributions. A suite of polycyclic aromatic hydrocarbons (PAHs) dominated by pyrene, fluoranthene and phenanthrene, typical of estuarine environments worldwide, and suites of mature sterane and hopane biomarkers were found to be most suitable as background markers for the Bay. A homologous series of long-chain n-aldehydes (C12-C32) with a strong even-over-odd carbon number dominance in the higher molecular weight range and the ubiquitous n-alkanes (n-C24-C34) with a strong odd-over-even carbon number dominance were utilized as terrigenous markers. Several ratios of these terrigenous and Bay markers were calculated for each station. These ratios and the statistical indicators from the multivariate analysis point toward a strong terrigenous signal in the terminus of South Bay and indicate net directional movement of recently introduced sediment where nontidal currents had been considered to be minimal or nonexistent and tidal currents had been assumed to be dominant.

California↗
USGS1988

Aliphatic hydrocarbons in sediments from Prydz Bay, Antarctica

High molecular weight aliphatic hydrocarbons were extracted from sediments at two sites (741 and 742) drilled during ODP Leg 119 in Prydz Bay. The distributions of n-alkanes and triterpenoid and steroid hydrocarbons suggest that the n- alkanes and steranes are mainly of terrestrial origin and that the hydrocarbons are immature to slightly mature in the Lower Cretaceous sediments and immature to mature in the Tertiary sediments. At Site 741, the Lower Cretaceous depositional sequence, which is generally characterized by immature hydrocarbons, is interrupted by sediment having more mature components, suggesting a change of source during part of Early Cretaceous time. At Site 742, the mature geochemical parameters of a Pliocene sample correlate with results reported elsewhere for Site 739. In all but one of the other Tertiary samples, the geochemical parameters indicate intermediate maturity. The Lower Cretaceous and Pliocene sediments average about 1.9% organic carbon, a value of interest from the point of view of potential sources of petroleum offshore of Antarctica.

Proceedings of the Ocean Drilling Program: Scienti↗
USGS1986

Petroleum associated with polymetallic sulfide in sediment from Gorda Ridge

A sediment sample, impregnated with asphaltic petroleum and polymetallic sulfide, was dredged from the southern end of Gorda Ridge (the Escanaba Trough) off northern California, within the offshore Exclusive Economic Zone of the United States. The molecular distributions of hydrocarbons in this petroleum show that it was probably derived from terrestrial organic matter in turbidite sediment filling the Escanaba Trough. Hydrothermal activity at the Gorda Ridge spreading center provided the heat for petroleum formation and was the source of fluids for sulfide mineralization.

California↗
USGS1982

Aliphatic Hydrocarbons in Surface Sediments of Willapa Bay and Grays Harbor, Washington

Willapa Bay and Grays Harbor are two adjacent estuaries along the coast of Washington state. Willapa Bay is a recreational area minimally affected by industry; Grays Harbor, on the other hand, is moderately industrialized. Aliphatic hydrocarbons in surface sediments from these two estuaries reflect the differences in human activities. For example, the mean concentration of aliphatic hydrocarbons for seven stations in Willapa Bay is 1,000 ?g/g (relative to organic carbon) while in Grays Harbor this mean concentration for six stations is 1,900 ?g/g. The difference is attributed mainly to the greater urban and industrial pollution in Grays Harbor. The gas chromatographic records of aliphatic hydrocarbons also reflect the extent of hydrocarbon pollution by the presence of a chromatographically unresolved mixture of hydrocarbons. This kind of mixture is more evident in sediments from Grays Harbor, and in both estuaries it is more concentrated in sediments collected nearest to urban centers.

Open-File Report↗
USGS1979

Biogenic and thermogenic gas in gas-charged sediment of Norton Sound, Alaska

Chemical and isotopic compositions of sediment gas from Norton Sound have been determined for near-surface, gas-charged sediments at two sites identified in acoustic profiles and bottom observations. At one site air-driven vibracorer penetrated sediment saturated with methane. The isotopic value suggests that the methane originated from active biological processes operating on peat in the top 4 m of sediment. At the other site, characterized by a large subsurface acoustic anomaly , smaller near-surface acoustic anomalies and active seepage of gas, the vibracorer obtained sediment saturated with gas composed of 98% CO2. Associated with the CO2 are minor concentrations of petroleum-like light hydrocarbons. The carbon isotopic compositions of CO2 and methane along with the chemical distribution of gaseous hydrocarbons indicate that at this site these gases are derived from thermal processes operating at depth in Norton Basin. Apparently CO2 from the decarbonation of marine limestone acts as a carrier for hydrocarbon gases that have been generated from organic matter buried in the basin. The gases reach the surface by faults and escape at the seafloor as a submarine seep. The presence of near-surface gas-charged sediment in Norton Sound reduces the stability of the seafloor. Areas where sediments are charged with gas may pose potential hazards for engineering developments.

Alaska↗
USGS1975

Short chain aliphatic acid anions in oil field waters and their contribution to the measured alkalinity

High alkalinity values found in some formation waters from Kettleman North Dome oil field are due chiefly to acetate and propionate ions, with some contribution from higher molecular weight organic acid ions. Some of these waters contain no detectable bicarbonate alkalinity. For waters such as these, high supersaturation with respect to calcite will be incorrectly indicated by thermodynamic calculations based upon carbonate concentrations inferred from traditional alkalinity measurements

Geochimica et Cosmochimica Acta↗
USGS1974

The chemical composition and estimated minimum thermal reservoir temperatures of the principal hot springs of northern and central Nevada

Fifty-five of the principal hot springs in northern and central Nevada have been sampled for chemical analyses. Major element constituents, sodium, potassium, calcium, and silica suggest minimum thermal-aquifer temperatures of 140°C or more at 16 of the hot spring complexes. At least five of the hot springs issue mixed waters which may indicate thermal-aquifer temperatures significantly lower than the true thermal-aquifer temperature. Sodium is the principal cation in almost all the spring waters. Four springs in northern Nye County and adjacent Eureka County have approximately equal amounts of sodium and calcium. Bicarbonate is the principal anion in most of the spring waters. However, the sampled hot springs on the western edge of the State have chloride as the principal anion. A diffuse zone of bicarbonate chloride waters with or without sulfate separates the chloride and bicarbonate regions.

Nevada↗
USGS1973

Silica-carbonate alteration of serpentine: Wall rock alteration in mercury deposits of the California Coast Ranges

Chemical, isotopic, and thermodynamic properties have been measured of CO 2 -rich ground waters in the central California Coast Ranges. The acidic CO 2 -rich waters react with serpentine to form silica-carbonate rock, the host rock of many mercury deposits in the Coast Range of California. In part the waters are of a metamorphic origin and in part the waters are locally derived meteoric waters. The CO 2 is entirely derived from metamorphic reactions at depth. Depending on the relative importance of several reactions, the relative abundances of silica and carbonate minerals vary in the silica-carbonate rock. If the CO 2 -rich fluids react directly with peridotite or dunite, massive magnesite deposits may form. © 1973 Society of Economic Geologists, Inc.

California↗