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George E. Claypool

Publications and source records attributed to George E. Claypool.

At least 19 recordsLinked to original sources
USGS2008

Natural gas geochemistry of sediments drilled on the 2005 Gulf of Mexico JIP cruise

In April and May 2005, cores were acquired and sub-sampled for gases in lease blocks Atwater Valley 13 and 14 and Keathley Canyon 151 during deep subseafloor drilling conducted as part of the JIP study of gas hydrates in the northern Gulf of Mexico. Sample types included sediment headspace gas, free gas derived from sediment gas exsolution, and gas exsolution from controlled degassing of pressurized cores. The gases measured both onboard and in shore-based labs were nitrogen, oxygen, hydrogen sulfide, carbon dioxide, and the hydrocarbons methane through hexane. The presence of seafloor mounds, seismic anomalies, a shallow sulfate-methane interface, and similar gas compositions and isotopic compositions near the seafloor and at depth suggest an upward flux of methane at both sites. Sediment gases at the Atwater Valley sites, where seafloor mounds and adjacent sediments were cored, strongly suggest a microbial source of methane, with very little thermogenic gas input. Sediment gas from all cores contained from about 96 to 99.9% methane, with the balance composed primarily of carbon dioxide. Methane to ethane ratios were greater than 1000, and often over 10,000. Gases from cores at Keathley Canyon were similar to those at Atwater Valley, however, deeper cores from Keathley Canyon contained more ethane, propane, and butane suggesting mixing with minor concentrations thermogenic gas. The isotopic composition of methane, ethane, and carbon dioxide were measured, and ??13C values range from -84.3 to -71.5???, -65.2 to -46.8???, and -23.5 to -3.0???, respectively, all consistent with microbial gas sources, early diagenesis of organic matter and perhaps biodegradation of petroleum. The presence of deep microbial gas at these sites here and elsewhere highlights a potentially significant, predominantly microbial gas source in the northern Gulf of Mexico.

Marine and Petroleum Geology↗
USGS2008

Petroleum systems of the San Joaquin Basin Province -- geochemical characteristics of gas types: Chapter 10 in Petroleum systems and geologic assessment of oil and gas in the San Joaquin Basin Province, California

The San Joaquin Basin Province is a petroliferous basin filled with predominantly Late Cretaceous to Pliocene-aged sediments, with organic-rich marine rocks of Late Cretaceous, Eocene, and Miocene age providing the source of most of the oil and gas. Previous geochemical studies have focused on the origin of the oil in the province, but the origin of the natural gas has received little attention. To identify and characterize natural gas types in the San Joaquin Basin, 66 gas samples were analyzed and combined with analyses of 15 gas samples from previous studies. For the purpose of this resource assessment, each gas type was assigned to the most likely petroleum system. Three general gas types are identified on the basis of bulk and stable carbon isotopic composition—thermogenic dry (TD), thermogenic wet (TW) and biogenic (B). The thermogenic gas types are further subdivided on the basis of the δ 13 C values of methane and ethane and nitrogen content into TD-1, TD-2, TD-Mixed, TW-1, TW-2, and TW-Mixed. Gas types TD-1 and TD-Mixed, a mixture of biogenic and TD-1 gases, are produced from gas fields in the northern San Joaquin Basin. Type TD-1 gas most likely originated from the Late Cretaceous to Paleocene Moreno Formation, a gas-prone source rock. The biogenic component of the TD-Mixed gas existed in the trap prior to the influx of thermogenic gas. For the assessment, these gas types were assigned to the Winters- Domengine Total Petroleum System, but subsequent to the assessment were reclassified as part of the Moreno-Nortonville gas system. Dry thermogenic gas produced from oil fields in the southern San Joaquin Basin (TD-2 gas) most likely originated from the oil-prone source rock of Miocene age. These samples have low wetness values due to migration fractionation or biodegradation. The thermogenic wet gas types (TW-1, TW-2, TW-Mixed) are predominantly associated gas produced from oil fields in the southern and central San Joaquin Basin. Type TW-1 gas most likely originates from source rocks within the Eocene Kreyenhagen Formation or the Eocene Tumey formation of Atwill (1935). Type TW-2 gas most likely originates from the Miocene Monterey Formation and equivalents. TW-Mixed gas is likely a mixture of biogenic and wet thermogenic gas (TW-1 or TW-2) derived from source rocks mentioned above. The thermogenic wet gas types are included in the corresponding Eocene or Miocene total petroleum systems. Type B gas is a dry, nonassociated gas produced from the Pliocene San Joaquin Formation in the central and southern San Joaquin Basin. This gas type most likely originated from Pliocene marine source rocks as a product of methanogenesis, and defines the Neogene Nonassociated Gas Total Petroleum System.

California↗
USGS1988

Organic geothermometry of petroleum from Escanaba Trough, offshore northern California

We have measured the extent of hopane and sterane isomerization and of monoaromatic-steroid-hydrocarbon aromatization in a sample of hydrothermally derived petroleum from the Escanaba Trough, a sediment-covered, volcanically active ridge axis. The results, along with kinetic parameters, predict the possible time-temperature history of the petrolum-forming process for this sample. The extent of these reactions is consistent with petroleum formation by intense heating (about 300–350°C) if the time period of this heating was as short as about 100 yr. Such a time scale is reasonable for hydrothermal-discharge events associated with ridge-crest volcanism.

California↗
USGS1986

Geochemical imprint of depositional conditions on organic matter in laminated—Bioturbated interbeds from fine-grained marine sequences

Laminated organic-rich shales are interbedded at a scale of centimeters to a few meters with bioturbated organic-poor mudstones or limestones in some fine-grained marine sequences. We have analyzed the organic matter in pairs of laminated/bioturbated interbeds from Cretaceous and Devonian rocks deposited in epicontinental and oceanic settings for the purpose of studying the influence of depositional and early diagenetic environment on the organic geochemical properties of marine shales. Results of these analyses indicate that for rocks that are still in a diagenetic stage of thermal alteration, the relative abundance of biomarker compounds and specific biomarker indices can be useful indicators of depositional and early diagenetic conditions. Pristane/phytane ratios are generally highest for laminated rocks from epicontinental basins and appear to reflect the input of isoprenoid precursors more than oxygenated versus anoxic depositional conditions. The thermally immature laminated rocks are characterized by relatively high contents of 17β(H), 21β(H)-hopanes, hopenes, sterenes and diasterenes, and by strong predominance of the 22R over 22S homohopane isomers. Thermally immature bioturbated samples are characterized by absence of the β,β-hopanes, by low contents of both saturated and unsaturated polycyclic hydrocarbons, and by slight or no predominance of the 22R over 22S homohopane isomers. There are less obvious compositional differences between the saturated hydrocarbons in the laminated and bioturbated units from the thermally mature sequences. For both the thermally mature and immature laminated samples, the degree of isomerization at the 22 C position for hopanes and at the 20 C position for steranes is generally consistent with the degree of thermal maturity interpreted from other properties of the organic matter. The bioturbated samples, however, exhibit inconsistent and anomalously high degrees of isomerization for the homohopanes, resulting either from reworking and oxidation of the primary organic matter or from the presence of older recycled organic matter.

Marine Geology↗
USGS1986

Depletion of 13C in Cretaceous marine organic matter: Source, diagenetic, or environmental sigal?

Geochemical studies of Cretaceous strata rich in organic carbon (OC) from Deep Sea Drilling Project (DSDP) sites and several land sections reveal several consistent relationships among amount of OC, hydrocarbon generating potential of kerogen (measured by pyrolysis as the hydrogen index, HI), and the isotopic composition of the OC. First, there is a positive correlation between HI and OC in strata that contain more than about 1% OC. Second, percent OC and HI often are negatively correlated with carbon isotopic composition (σ 13 C) of kerogen. The relationship between HI and OC indicates that as the amount of organic matter increases, this organic matter tends to be more lipid rich reflecting the marine source of the organic matter. Cretaceous samples that contain predominantly marine organic matter tend to be isotopically lighter than those that contain predominantly terrestrial organic matter. Average σ 13 C values for organic matter from most Cretaceous sites are between −26 and −28‰, and values heavier than about −25‰ occur at very few sites. Most of the σ 13 C values of Miocene to Holocene OC-rich strata and modern marine plankton are between −16 to −23‰. Values of σ 13 C of modern terrestrial organic matter are mostly between −23 and −33‰. The depletion of terrestial OC in 13 C relative to marine planktonic OC is the basis for numerous statements in the literature that isotopically light Cretaceous organic matter is of terrestrial origin, even though other organic geochemical and(or) optical indicators show that the organic matter is mainly of marine origin. A difference of about 5‰ in σ 13 C between modern and Cretaceous OC-rich marine strata suggests either that Cretaceous marine planktonic organic matter had the same isotopic signature as modern marine plankton and that signature has been changed by diagenesis, or that OC derived from Cretaceous marine plankton was isotopically lighter by about 5‰ relative to modern plankton OC. Diagenesis does not produce a significant shift in σ 13 C in Miocene to Holocene sediments, and therefore probably did not produce the isotopically light Cretaceous OC. This means that Cretaceous marine plankton must have had σ 13 C values that were about 5‰ lighter than modern marine plankton, and at least several per mil lighter than Cretaceous terrestrial vegetation. The reason for these lighter values, however, is not obvious. It has been proposed that concentrations of CO 2 were higher during the middle Cretaceous, and this more available CO 2 may be responsible for the lighter σ 13 C values of Cretaceous marine organic matter.

Marine Geology↗
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↗
USGS1986

Isotopic composition of interstitial fluids in sediment of the Nankai Trough, Deep Sea Drilling Project Leg 87

The isotopic compositions of dissolved CO2 and CH4 in sediments of the Nankai Trough indicate that CH4 is formed during early diagenesis by microbial reduction of CO2 . At the shallowest sampled depths, the CO2 dissolved in the pore water is unusually enriched in 12C (δ13C = - 35.2‰), indicating contribution of CO2 from oxidation of CH4 . The most intense microbiological activity appears to be confined to the uppermost 50 m of sediment, based on relative lack of change in the isotopic compositions below this depth. Gas hydrate probably is not present at these localities (Sites 582, 583) because of CH4 concentrations that are insufficient to saturate the pore water with respect to gas hy drate stability

Initial Reports of the D.S.D.P.↗
USGS1985

Anomalous 13C enrichment in modern marine organic carbon

Marine organic carbon is heavier isotopically (13C enriched) than most land-plant or terrestrial organic C1. Accordingly, ??13C values of organic C in modern marine sediments are routinely interpreted in terms of the relative proportions of marine and terrestrial sources of the preserved organic matter2,3. When independent geochemical techniques are used to evaluate the source of organic matter in Cretaceous or older rocks, those rocks containing mostly marine organic C are found typically to have lighter (more-negative) ??13C values than rocks containing mostly terrestrial organic C. Here we conclude that marine photosynthesis in mid-Cretaceous and earlier oceans generally resulted in a greater fractionation of C isotopes and produced organic C having lighter ??13C values. Modern marine photosynthesis may be occurring under unusual geological conditions (higher oceanic primary production rates, lower PCO2) that limit dissolved CO2 availability and minimize carbon isotope fractionation4. ?? 1985 Nature Publishing Group.

Nature↗
USGS1985

Comparative geochemical and mineralogical studies of two cyclic transgressive pelagic limestone units, cretaceous Western Interior Basin, U.S.

Pelagic limestone units were deposited in the North American Western Interior seaway during two major Cretaceous transgressive episodes. The Bridge Creek Limestone Member of the Greenhorn Formation, deposited during the Late Cenomanian-Early Turonian transgression, and the Smoky Hill Member of the Niobrara Formation, deposited during the overall Early Coniacian-Early Campanian transgression, are both enriched in organic-carbon and exhibit smallscale carbonate cycles representing periodicities in the range 20 to 40 ky. The distinct periodicity and overall unusual depositional milieu of both units are reflected in their sedimentary structures, mineralogy, and geochemistry. The Bridge Creek Limestone at Pueblo, Colorado, averages 78% CaCO 3 and 1.75% organic carbon with ranges of 42-96% and 0.06-6.97%, respectively, across small-scale cycles. High concentrations of Al, Fe, Mg, K, Ti, Na, Cr, Ni, V; higher Sr/Ca and lower Si/Al ratios; and lighter δ 18 0 in CaCO 3 in dark-colored clay-rich beds all suggest periodic influx of terrestrial clay minerals during times of peak fresh water runoff from uplifted highlands to the west. Higher Sr/Ca ratios in marlstone beds than in limestone beds suggest that the marlstone beds have undergone less diagenetic removal of Sr. Higher concentrations of organic carbon, hydrogen, and sulfur, and preservation of some lamination in the clay-rich beds also suggest that the times of enhanced runoff may have induced stable salinity stratification in the water column, which led to gradual depletion of dissolved oxygen in the bottom waters and enhanced preservation of organic carbon in sediments. The geochemistry also suggests that a significant change in sedimentation occurred at the Cenomanian-Turonian boundary. The geochemical characteristics of the Niobrara Formation near Fort collins, Colorado, are very similar to those of the Bridge Creek Limestone at Pueblo, suggesting similar depositional conditions and source of clastic materials. However, the small scale cycles are present but more subdued in the Niobrara Formation than in the Bridge Creek Limestone, and the Niobrara Formation in the Fort Collins area has not been as altered by diagenesis.

SEPM Special Publication↗
USGS1984

The Kingak shale of northern Alaska—regional variations in organic geochemical properties and petroleum source rock quality

The Kingak Shale, a thick widespread rock unit in northern Alaska that ranges in age from Early Jurassic through Early Cretaceous, has adequate to good oil source rock potential. This lenticular-shaped rock unit is as much as 1200 m thick near the Jurassic shelf edge, where its present-day burial depth is about 5000 m. Kingak sediment, transported in a southerly direction, was deposited on the then marine continental shelf. The rock unit is predominantly dark gray Shale with some interbeds of thick sandstone and siltstone. The thermal maturity of organic matter in the Kingak Shale ranges from immature (<0.6% R 0 ) on the Barrow arch to postmature (>2.0% R 0 ) in the Colville basin toward the south. Its organic carbon and hydrogen contents are highest in the eastern part of northern Alaska south of and around the Kuparuk and Prudhoe Bay oil fields. Carbon isotope data of oils and rock extracts indicate that the Kingak Shale is a source of some North Slope oil, but is probably not the major source.

Alaska↗
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↗
USGS1984

Accumulation of organic matter in Cretaceous oxygen-deficient depositional environments in the central Pacific Ocean

Complete records of organic-carbon-rich Cretaceous strata were continuouslycored on the flanks of the Mid-Pacific Mountains and southern Hess Rise in the central North Pacific Ocean during DSDP Leg 62. Organic-carbon-rich laminated silicified limestones were deposited in the western Mid-Pacific Mountains during the early Aptian, a time when that region was south of the equator and considerably shallower than at present. Organic-carbon-rich, laminated limestone on southern Hess Rise overlies volcanic basement and includes 136 m of stratigraphic section of late Albian to early Cenomanian age. This limestone unit was deposited rapidly as Hess Rise was passing under the equatorial high-productivity zone and was subsiding from shallow to intermediate depths. The association of volcanogenic components with organic-carbon-rich strata on Hess Rise in the Mid-Pacific Mountains is striking and suggests that there was a coincidence of mid-plate volcanic activity and the production and accumulation of organic matter at intermediate water depths in the tropical Pacific Ocean during the middle Cretaceous. Pyrolysis assays and analyses of extractable hydrocarbons indicate that the organic matter in the limestone on Hess Rise is composed mainly of lipid-rich kerogen derived from aquatic marine organisms and bacteria. Limestones from the Mid-Pacific Mountains generally contain low ratios of pyrolytic hydrocarbons to organic carbon and low hydrogen indices, suggesting that the organic matter may contain a significant proportion of land-derived material, possibly derived from numerous volcanic islands that must have existed before the area subsided. The organic carbon in all samples analyzed is isotopically light ( δ 13 C − 24 to − 29 per mil) relative to most modern rine organic carbon, and the lightest carbon is also the most lipid-rich. There is a positive linear correlation between sulfur and organic carbon in samples from Hess Rise and from the Mid-Pacific Mountains. The slopes and intercepts of C-S regression lines however, are different for each site and all are different from regression lines for samples from modern anoxic marine sediments and from Black Sea cores. The organic-carbon-rich limestones on Hess Rise, the Mid-Pacific Mountains, and other plateaus and seamounts in the Pacific Ocean are not synchronous but do occur within the same general middle Cretaceous time period as organic-carbon-rich lithofacies elsewhere in the world ocean, particularly in the Atlantic Ocean. Strata of equivalent age in the deep basins of the Pacific Ocean are not rich in organic carbon, and were deposited in oxygenated environments. This observation, together with the evidence that the plateau sites were considerably shallower and closse to the equator during the middle Creataceous suggests that local tectonic and hydrographic conditions may have resulted in high surface-water productivity and the preservation of organic matter in an oxygen-deficient environment where an expanded mid-water oxygen minimum developed and impinged on elevated platforms and seamounts.

Organic Geochemistry↗
USGS1981

Petroleum geology of Cook Inlet basin: An exploration model

Oil exploration commenced onshore adjacent to lower Cook Inlet on the Iniskin Peninsula in 1900, shifted with considerable success to upper Cook Inlet from 1957 through 1965, then returned to lower Cook Inlet in 1977 with the COST well and Federal OCS sale. Lower Cook Inlet COST No. 1 well, drilled to a total depth of 3,775.6 m, penetrated basinwide unconformities at the tops of Upper Cretaceous, Lower Cretaceous, and Upper Jurassic strata at 797.1, 1,540.8, and 2,112.3 m, respectively. Sandstone of potential reservoir quality is present in the Cretaceous and lower Tertiary rocks. All siltstones and shales analyzed are low (0 to 0.5 wt. %) in oil-prone organic matter, and only coals are high in humic organic matter. At total depth, vitrinite readings reached a maximum ave age reflectance of 0.65. Several indications of hydrocarbons were present. Oil analyses suggest that oils from the major fields of the Cook Inlet region, most of which produce from the Tertiary Hemlock Conglomerate, have a common source. More detailed work on stable carbon isotope ratios and the distribution of gasoline-range and heavy (C 12 + ) hydrocarbons confirms this genetic relation among the major fields. In addition, oils from Jurassic rocks under the Iniskin Peninsula and from the Hemlock Conglomerate at the southwestern tip of the Kenai lowland are members of the same or a very similar oil family. The Middle Jurassic strata of the Iniskin Peninsula are moderately rich in organic carbon (0.5 to 1.5 wt. %) and yield shows of oil and of gas in wells and in surface seeps. Extractable hydrocarbons from this strata are similar in chemi al and isotopic composition to the Cook Inlet oils. Organic matter in Cretaceous and Tertiary rocks is thermally immature in all wells analyzed. Oil reservoirs in the major producing fields are of Tertiary age and unconformably overlie Jurassic rocks; the pre-Tertiary unconformity may be significant in exploration for new oil reserves. The unconformable relation between reservoir rocks and likely Middle Jurassic source rocks also implies a delay in the generation and expulsion of oil from Jurassic until late Tertiary when localized basin subsidence and thick sedimentary fill brought older, deeper rocks to the temperature required for petroleum generation. Reservoir porosities, crude oil properties, the type of oil field traps, and the tectonic framework of the oil fields on the west flank of the basin provide evidence used to reconstruct an oil migration route. The route is inferred to commence deep in the truncated Middle Jur ssic rocks and pass through the porous West Foreland Formation in the McArthur River field area to a stratigraphic trap in the Oligocene Hemlock Conglomerate and the Oligocene part of the Tyonek Formation at the end of Miocene time. Pliocene deformation shut off this route and created localized structural traps, into which the oil moved by secondary migration to form the Middle Ground Shoal, McArthur River, and Trading Bay oil fields. Oil generation continued into the Pliocene, but this higher API gravity oil migrated along a different route to the Granite Point field.

Alaska↗
USGS1981

Origin of organic-carbon-rich mid-Cretaceous limestones, Mid-Pacific Mountains and southern Hess Rise

Limestones of mid-Cretaceous age containing as much as 8.6 percent organic carbon were cored at one site (463) in the Mid-Pacific Mountains and at two sites (465, 466) on southern Hess Rise, central North Pacific Ocean, during Leg 62 of the Deep Sea Drilling Project. In the Mid-Pacific Mountains, three layers containing more than 2% organic carbon are associated with volcanic ash in silicified limestone of early Aptian age (—112-113 m.y. old), a time when the site was south of the equator and considerably shallower than at present (2525 m). The beds of laminated, organiccarbon-rich limestone, implying deposition in an oxygen-deficient environment, are interbedded with normal pelagic limestones. This sequence lies on interbedded pelagic limestones and clastic limestones containing locally derived shallow-water carbonate debris, and it is overlain by interbedded green, gray, and pink limestones. The organic-carbonrich strata on southern Hess Rise are dark-olive, laminated limestones with rare interbeds of altered volcanic ash of the late Aptian to early Cenomanian ( — 98 to 103 m.y. old), a time when the site was passing under the equatorial highproductivity zone and subsiding from shallow to intermediate water depths. The organic-carbon-rich limestone sequence overlies volcanic basement (trachyte) in this part of Hess Rise. The association of volcanogenic sediments with organic-carbon-rich strata on Hess Rise is not as striking as in the Mid-Pacific Mountains, but the occurrences do suggest a coincidence of mid-plate volcanic activity and accumulation of organic matter at intermediate water depths in the tropical North Pacific Ocean during the mid-Cretaceous. Pyrolysis assays indicate that most of the organic matter in the limestone on Hess Rise is composed of lipid-rich kerogen derived from marine organisms. Limestones from the Mid-Pacific Mountains contain lower concentrations of organic matter. Pyrolysis assays and extractable hydrocarbons indicate that the organic matter in samples from Hole 463 is also predominantly of marine origin, and that contributions of terrigenous organic matter were probably minor. Analyses of stable carbon isotopes indicate that the organic carbon in all analyzed samples is isotopically light (δ13C 24 to - 29‰) relative to most modern marine organic carbon (δ13C - 9 to - 30%), and that the lightest carbon (δ13C 28 to - 29‰) is also the most lipid-rich. The organic-carbon-rich mid-Cretaceous limestones on Hess Rise, the Mid-Pacific Mountains, and other elevated plateaus and seamounts in the Pacific Ocean are approximately equivalent in age (mid-Cretaceous, -85-120 m.y.) to organic-carbon-rich lithofacies elsewhere in the world ocean, particularly in the Atlantic Ocean and parts of the Indian Ocean. However, strata of equivalent age deposited in the Pacific Ocean at greater depths do not contain any carbon rich horizons. This observation, together with the evidence that the plateau sites were considerably shallower and close to the equator during the mid-Cretaceous, suggests that an expanded mid-water oxygen minimum, together with local restrictions in circulation, may have resulted in the preservation of organic matter in an oxygen-deficient environment where the oxygen minimum impinged on elevated platforms such as Hess Rise and the Mid-Pacific Mountains.

Initial reports of the Deep Sea Drilling Project↗