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K.A. Kvenvolden

Publications and source records attributed to K.A. Kvenvolden.

At least 55 records · Page 3Linked to original sources
USGS1993

Possible connection between two Alaskan catastrophes occurring 25 yr apart (1964 and 1989)

On March 24, 1989, the Exxon Valdez supertanker grounded on Bligh Reef, spilling North Slope crude oil into Prince William Sound, Alaska. Tracking the geochemical fate of this spilled oil has revealed, in addition to weathered products from the spill, minor oil residues on beaches from a distinctly different source. By using carbon isotopic compositions of whole-oil residues as a principal method of identification, we found that the δ 13 C values of Exxon Valdez oil (one sample) and its residues (eight samples from six islands) average -29.3 ±0.1‰. In contrast, the non- Exxon Valdez residues (15 samples from 12 localities) have an average δ 13 C value of -23.8 ±0.1‰. This tight distribution of carbon isotopic values suggests a single event to explain the non- Exxon Valdez residues. This event likely was the Great Alaska Earthquake of March 27, 1964. This quake and the subsequent tsunami destroyed asphalt storage facilities at the old Valdez town site, spilling asphalt (δ 13 C = -23.6‰) into Port Valdez fjord. From there the asphalt apparently advanced south into the sound. Thus, the possible connection between two Alaskan catastrophes, separated by 25 yr, is found in the minor oil- like residues that continue to mark the two events on the beaches of Prince William Sound.

Geology↗
USGS1993

Methane in permafrost - Preliminary results from coring at Fairbanks, Alaska

Permafrost has been suggested as a high-latitude source of methane (a greenhouse gas) during global warming. To begin to assess the magnitude of this source, we have examined the methane content of permafrost in samples from shallow cores (maximum depth, 9.5m) at three sites in Fairbanks, Alaska, where discontinuous permafrost is common. These cores sampled frozen loess, peat, and water (ice) below the active layer. Methane contents of permafrost range from <0.001 to 22.2mg/kg of sample. The highest methane content of 22.2mg/kg was found in association with peat at one site. Silty loess had high methane contents at each site of 6.56, 4.24, and 0.152mg/kg, respectively. Carbon isotopic compositions of the methane (??13C) ranged from -70.8 to -103.9 ???, and hydrogen isotopic compositions of the methane (??D) from -213 to -313 ???, indicating that the methane is microbial in origin. The methane concentrations were used in a one dimensional heat conduction model to predict the amount of methane that will be released from permafrost worldwide over the next 100 years, given two climate change scenarios. Our results indicate that at least 30 years will elapse before melting permafrost releases important amounts of methane; a maximum methane release rate will be about 25 to 30 Tg/yr, assuming that methane is generally distributed in shallow permafrost as observed in our samples.

Conference Paper↗
USGS1992

Use of geochemical biomarkers in bottom sediment to track oil from a spill, San Francisco Bay, California

In April 1988, approximately 1500 m3 of a San Joaquin Valley crude oil were accidentally released from a Shell Oil Co. refinery near Martinez, Californa. The oil flowed into Carquinez Strait and Suisun Bay in northern San Francisco Bay Sediment and oil samples were collected within a week and analysed for geochemical marker compounds in order to track the molecular signature of the oil spill in the bottom sediment. Identification of the spilled oil in the sediment was complicated by the degraded nature of the oil and the similarity of the remaining, chromatographically resolvable constituents to those already present in the sediments from anthropogenic petroleum contamination, pyrogenic sources, and urban drainage. Ratios of hopane and sterane biomarkers, and of polycyclic aromatic hydrocarbons and their alkylated derivatives best identified the oil impingement. They showed the oil impact at this early stage to be surficial only, and to be patchy even within an area of heavy oil exposure.

California↗
USGS1990

Characterization of hydrocarbon gas within the stratigraphic interval of gas-hydrate stability on the North Slope of Alaska, U.S.A.

In the Kuparuk River Unit 2D-15 well, on the North Slope of Alaska, a 60 m-thick stratigraphic interval that lies within the theoretical pressure-temperature field of gas-hydrate stability is inferred to contain methane hydrates. This inference is based on interpretations from well logs: (1) release of methane during drilling, as indicated by the mud log, (2) an increase in acoustic velocity on the sonic log, and (3) an increase of electrical resistivity on the electric logs. Our objective was to determine the composition and source of the gas within the shallow gas-hydrate-bearing interval based on analyses of cutting gas. Headspace gas from canned drill cuttings collected from within the gas-hydrate-bearing interval of this well has an average methane to ethane plus propane [C 1 /(C 2 + C 3 )] ratio of about 7000 and an average methane δ 13 C value of −46% (relative to the PDB standard). These compositions are compared with those obtained at one well located to the north of 2D-15 along depositional strike and one down-dip well to the northeast. In the well located on depositional strike (Kuparuk River Unit 3K-9), gas compositions are similar to those found at 2D-15. At the down-dip well (Prudhoe Bay Unit R-1), the C 1 /(C 2 +C 3 ) ratios are lower (700) and the methane δ 13 C is heavier (−33%). We conclude that the methane within the stratigraphic interval of gas hydrate stability comes from two sources— in situ microbial gas and migrated thermogenic gas. The thermal component is greatest at Prudhoe Bay. Up-dip to the west, the thermogenic component decreases, and microbial gas assumes more importance.

Alaska↗
USGS1990

Hydrocarbon geochemistry of hydrothermally generated petroleum from Escanaba trough, offshore California U.S.A.

In 1986, three samples of sulfide-rich sediments, impregnated with hydrothermally derived, asphaltic petroleum, were recovered in a dredge and by submersible from Escanaba Trough, the sediment-covered, southern end of the Gorda Ridge spreading axis, offshore northern California. The molecular distributions of hydrocarbons in the two pyrrhotite-rich samples recovered by submersible are similar and compare well the hydrocarbon composition of the first pyrrhotite-rich samples containing petroleum discovered at a 1985 dredge site about 30 km to the south of the site of the submersible dive. In contrast, the 1986 dredge sample, composed of a polymetallic assemblage of sulfides, containes petroleum in which the distribution of hydrocarbons indicates a slightly higher of maturity relative to the other samples. The observation that petroleum of variable composition occurs with metallic sulfides at two and probably more distinct site indicates that petroleum generation may be a common process in the hydrothermally active Escanaba Trough.

California↗
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↗
USGS1989

Hydrocarbon gas seeps of the convergent Hikurangi margin, North Island, New Zealand

Two hydrocarbon gas seeps, located about 13 km apart, have distinctive molecular and isotopic compositions. These seeps occur within separate tectonic melange units of narrow parallel trending and structurally complex zones with incorporated upper Cretaceous and Palaeogene passive continental margin deposits which are now compressively deformed and imbricated along the convergent Hikurangi margin of North Island, New Zealand. At Brookby Station within the Coastal High, the seeping hydrocarbon gas has a methane/ethane ratio of 48 and ??13C and ??D values of methane of -45.7 and -188???, respectively (relative to the PDB and SMOW standards). Within the complex core of the Elsthorpe Anticline at Campbell Station seep, gas has a methane/ethane ratio of about 12000, and the methane has ??13C and ??D values of -37.4 and -170???, respectively. The source of the gases cannot be positively identified, but the gases probably originate from the thermal decomposition of organic matter in tectonically disturbed upper Cretaceous and/or lower Tertiary sedimentary rocks of passive margin affinity and reach the surface by migration along thrust faults associated with tectonic melange. The geochemical differences between the two gases may result from differences in burial depths of similar source sediment. ?? 1989.

Marine and Petroleum Geology↗
USGS1989

Map showing the depth to the base of the deepest ice-bearing permafrost as determined from well logs, North Slope, Alaska

Because gas hydrates from within a limited temperature range, subsurface equilibrium temperature data are necessary to calculate the depth and thickness of the gas-hydrate stability field. Acquiring these data is difficult because drilling activity often disrupts equilibrium temperatures in the subsurface, and a well mush lie undisturbed until thermal equilibrium is reestablished (Lachenbruch and Brewer, 1959). On the North Slope if Akaska, a series of 46 oil and gas exploratory wells, which were considered to be near thermal equilibrium (Lachenbruch and others, 1982; 1987), were surveyed with high-resolution temperature devices (see table 1). However, several thousand other exploratory and production wells have been drilled on the North Slope, and although they do not include temperature profiles, their geophysical logs often allow descrimination between ice-bearing and non-ice-bearing strata. At the outset of this study, the coincidence of the base of ice-bearing strata being near the same depth as the 0 &deg;C isotherm at Prudhoe Bay (Lachenbruch and others, 1982) appeared to offer an opportunity to quickly and inexpensively expand the size of our subsurface temperature data base merely by using well logs to identify the base of the ice-bearing strata.

Alaska↗
USGS1988

Hydrocarbon gas in sediment of the Southern Pacific Ocean

Methane, ethane, ethene, propane, and propene are common hydrocarbon gases in near-surface sediment from offshore areas in the southern Pacific Ocean near Papua New Guinea, the Solomon Islands, Vanuatu, Tonga, New Zealand, and Antarctica. Sea floor sites for sampling of sediment were selected on the basis of anomalies in marine seismic records, and the samples were intentionally biased toward finding possible thermogenic hydrocarbon gases. In none of the areas, however, were thermogenic hydrocarbons clearly identified. The hydrocarbon gases that were found appear to be mainly the products of in situ microbial processes. ?? 1988 Springer-Verlag New York Inc.

Geo-Marine Letters↗
USGS1988

Methane hydrate - A major reservoir of carbon in the shallow geosphere?

Methane hydrates are solids composed of rigid cages of water molecules that enclose methane. Sediment containing methane hydrates is found within specific pressure-temperature conditions that occur in regions of permafrost and beneath the sea in outer continental margins. Because methane hydrates are globally widespread and concentrate methane within the gas-hydrate structure, the potential amount of methane present in the shallow geosphere at subsurface depths of < ???2000 m is very large. However, estimates of the amount are speculative and range over about three orders of magnitude, from 2 ?? 103 to 4 ?? 106 Gt (gigatons = 1015 g) of carbon, depending on the assumptions made. The estimate I favor is ??? 1 ?? 104 Gt of carbon. The estimated amount of organic carbon in the methane-hydrate reservoir greatly exceeds that in many other reservoirs of the global carbon cycle - for example, the atmosphere (3.6 Gt); terrestrial biota (830 Gt); terrestrial soil, detritus and peat (1960 Gt); marine biota (3 Gt); and marine dissolved materials (980 Gt). In fact, the amount of carbon may exceed that in all fossil fuel deposits (5 ?? 103 Gt). Because methane hydrates contain so much methane and occur in the shallow geosphere, they are of interest as a potential resource of natural gas and as a possible source of atmospheric methane released by global warming. As a potential resource, methane hydrates pose both engineering and production problems. As a contributor to a changing global climate, destabilized methane hydrates, particularly those in shallow, nearshore regions of the Arctic Ocean, may have some effect, but this effect will probably be minimal, at least during the next 100 years. ?? 1988.

Chemical Geology↗