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At least 919 records · Page 51Linked to original sources
USGS2011

Feature-based and statistical methods for analyzing the Deepwater Horizon oil spill with AVIRIS imagery

The Deepwater Horizon oil spill covered a very large geographical area in the Gulf of Mexico creating potentially serious environmental impacts on both marine life and the coastal shorelines. Knowing the oil's areal extent and thickness as well as denoting different categories of the oil's physical state is important for assessing these impacts. High spectral resolution data in hyperspectral imagery (HSI) sensors such as Airborne Visible and Infrared Imaging Spectrometer (AVIRIS) provide a valuable source of information that can be used for analysis by semi-automatic methods for tracking an oil spill's areal extent, oil thickness, and oil categories. However, the spectral behavior of oil in water is inherently a highly non-linear and variable phenomenon that changes depending on oil thickness and oil/water ratios. For certain oil thicknesses there are well-defined absorption features, whereas for very thin films sometimes there are almost no observable features. Feature-based imaging spectroscopy methods are particularly effective at classifying materials that exhibit specific well-defined spectral absorption features. Statistical methods are effective at classifying materials with spectra that exhibit a considerable amount of variability and that do not necessarily exhibit well-defined spectral absorption features. This study investigates feature-based and statistical methods for analyzing oil spills using hyperspectral imagery. The appropriate use of each approach is investigated and a combined feature-based and statistical method is proposed.

Proceedings of SPIE↗
USGS1980

Variability of currents and sediment transport on continental shelves: Optical and current meter studies of the bottom boundary layer

The Continental Margin Sediment Dynamics program of the U.S. Geological Survey has been using a variety of optical instruments to monitor water turbidity as part of our studies of sediment transport. Although we suspect that optical devices will eventually be supplanted by more direct measures of suspended sediments, results of several field experiments indicate that for now transmissometers and nephelometers offer the best solution to the problem of long term environmental monitoring in the ocean. The Continental Margin Sediment Dynamics (CMSD) program of the U.S. Geological Survey is structured to investigate those oceanographic and geological processes which influence and control the active transport of sediments and other materials over continental margins. The focus of this program is on active sedimentary processes, the mechanisms which create them, and the effects they produce (see Figure 1 for a diagrammatic depiction). Basically, we design our experiments to investigate (1) transport mechanisms of oceanic sediments and other materials as suspended load and bed load, and (2) relationships of erosion and deposition to the dynamical characteristics of oceanic bottom boundary layers. The purpose of this report is to describe briefly those aspects of equipment and experiments that relate to our study of suspended particulate matter and water turbidity. Much of our understanding of the spatial distribution and temporal variability of suspended sediments depends upon measurements from optical instruments. In this report we describe those instruments and give examples of their use and some results of two field experiments.

Proceedings of SPIE↗
USGS2011

Assessing the natural performance of felsic tuffs using the Rb-Sr and Sm-Nd systems-A study of the altered zone in the Topopah Spring Member, Paintbrush Tuff, Yucca Mountain, Nevada

Core samples of the Topopah Spring Member of the Paintbrush Tuff from drill hole UE25A#1 were analyzed for Sr and Nd isotopes and selected minor and trace elements to constrain the origin of a zcolitized zone associated with the lower vitrophyre. The Sm-Nd radiogenic isotope system was unperturbed by the alteration, but the Rb-Sr system was severely disturbed in the altered zone. The thick, densely welded high-silica rhyolite is remarkably uniform in composition with only a slight decrease in initial 87 Sr/ 86 Sr ratios with depth (0.7129–0.7125). Quartz latite in the upper part of the Topopah Spring has significantly lower initial Sr isotope ratios (0.7095–0.7114). Locally in the altered zone, Sr and Ca were gained in substantial amounts, and K, Rb, and Y were removed. Ti, Zr, Nb, Ba, La, Ce, Sm, and Nd were relatively immobile during the alteration. Sr added to the altered zone had an isotopic composition of 0.7119 ± 0.0002 and was probably derived from dissolution of glass in the bulk Topopah Spring (high silica rhyolite + quartz latite) and transported downward by infiltration.

Nevada↗
USGS2011

The modeler's influence on calculated solubilities for performance assessments at the Aspo Hard-rock Laboratory

Four researchers were asked to provide independent modeled estimates of the solubility of a radionuclide solid phase, specifically Pu(OH) 4 , under five specified sets of conditions. The objectives of the study were to assess the variability in the results obtained and to determine the primary causes for this variability. In the exercise, modelers were supplied with the composition, pH and redox properties of the water and with a description of the mineralogy of the surrounding fracture system A standard thermodynamic data base was provided to all modelers. Each modeler was encouraged to use other data bases in addition to the standard data base and to try different approaches to solving the problem. In all, about fifty approaches were used, some of which included a large number of solubility calculations. For each of the five test cases, the calculated solubilities from different approaches covered several orders of magnitude. The variability resulting from the use of different thermodynamic data bases was in most cases, far smaller than that resulting from the use of different approaches to solving the problem.

Materials Research Society Symposium - Proceedings↗
USGS2024

Fair graph learning using constraint-aware priority adjustment and graph masking in river networks

Accurate prediction of water quality and quantity is crucial for sustainable development and human well-being. However, existing data-driven methods often suffer from spatial biases in model performance due to heterogeneous data, limited observations, and noisy sensor data. To overcome these challenges, we propose Fair-Graph, a novel graph-based recurrent neural network that leverages interrelated knowledge from multiple rivers to predict water flow and temperature within large-scale stream networks. Additionally, we introduce node-specific graph masks for information aggregation and adaptation to enhance prediction over heterogeneous river segments. To reduce performance disparities across river segments, we introduce a centralized coordination strategy that adjusts training priorities for segments. We evaluate the prediction of water temperature within the Delaware River Basin, and the prediction of streamflow using simulated data from U.S. National Water Model in the Houston River network. The results showcase improvements in predictive performance and highlight the proposed model's ability to maintain spatial fairness over different river segments.

Delaware River basin↗
USGS2025

Physics-guided fair graph sampling for water temperature prediction in river networks

This work introduces a novel graph neural networks (GNNs)-based method to predict stream water temperature and reduce model bias across locations of different income and education levels. Traditional physics-based models often have limited accuracy because they are necessarily approximations of reality. Recently, there has been an increasing interest of using GNNs in modeling complex water dynamics in stream networks. Despite their promise in improving the accuracy, GNNs can bring additional model bias through the aggregation process, where node features are updated by aggregating neighboring nodes. The bias can be especially pronounced when nodes with similar sensitive attributes are frequently connected. We introduce a new method that leverages physical knowledge to represent the node influence in GNNs, and then utilizes physics-based influence to refine the selection and weights over the neighbors. The objective is to facilitate equitable treatment over different sensitive groups in the graph aggregation, which helps reduce spatial bias over locations, especially for those in underprivileged groups. The results on the Delaware River Basin demonstrate the effectiveness of the proposed method in preserving equitable performance across locations in different sensitive groups.

Proceedings of the AAAI Conference on Artificial I↗
USGS1997

Kansas geological survey's Digital Petroleum Atlas (DPA) project

The Kansas Digital Petroleum Atlas (DPA) is a new approach to generating and publishing petroleum reservoir, field, play and basin studies. Atlas products are available anywhere in the world using a standard point-and-click World-Wide-Web interface. All information and technology in the DPA can be accessed, manipulated and downloaded in order to provide efficient transfer of the technology for client-defined solutions. The DPA design provides a dynamic product that is constantly evolving through new information structures, the latest research results, and incorporation of additional data. Through complete and flexible user access to both interpretative products and underlying reservoir and well data, the DPA significantly alters the relationship between research results, data access, and the transfer of technology.

Proceedings - SPE Annual Technical Conference and ↗
USGS2002

Integrated biostratigraphic and radiometric study on the Lower Cenomanian (Cretaceous) of Hokkaido, Japan

New 40 Ar- 39 Ar total fusion ages have been obtained on sanidine from tuffs in the zone of Mantelliceras saxbii (equivalent to the same subzone of the European ammonite zonation) and the zone of Graysonites wooldridgei (equivalent to the European subzone of Neostlingoceras carcitanense ). Ages of 98.98±0.38 Ma and 99.16±0.37 Ma, for these zones, respectively, place new constraints on the age of the AlbianlCenomanian boundary. If the base of the Cenomanian is to be defined, as currently proposed, as the FAD of the planktonic foraminifera Rotalipora globotruncanoides then the Albian/Cenomanian boundary will be at least as old as 99.2±0.4 Ma. Some 50±10m of undated sediments lie below the lowest find of R . globotruncanoides and above bono fide uppermost Albian strata.

Hokkaido↗
USGS2001

Leg 188 synthesis: Transitions in the glacial history of the Prydz Bay region, East Antarctica, from ODP drilling

Drilling during Leg 119 (1988) and Leg 188 (2000; Sites 1165–1167) of the Ocean Drilling Program (ODP) provides direct evidence for long- and short-term changes in Cenozoic paleoenvironments in the Prydz Bay region. Cores from across the continental margin reveal that in preglacial times the present shelf was an alluvial plain system with austral conifer woodland in the Late Cretaceous that changed to cooler Nothofagus rainforest scrub by the middle to late Eocene (Site 1166). Earliest recovered evidence of nearby mountain glaciation is seen in late Eocene–age grain textures in fluvial sands. In the late Eocene to early Oligocene, Prydz Bay permanently shifted from being a fluvio-deltaic complex to an exclusively marine continental shelf environment. This transition is marked by a marine flooding surface later covered by overcompacted glacial sediments that denote the first advance of the ice sheet onto the shelf. Cores do not exist for the early Oligocene to early Miocene, and seismic data are used to infer the transition from a shallow to normal depth prograding continental shelf with submarine canyons on the slope and channel/levees on the rise. Cores from the continental rise at Site 1165 show long-term (millions of years) early Miocene and younger decreases in sedimentation rates as well as short-term (Milankovitch periods) cyclicity between principally biogenic and terrigenous sediment supply—resulting from the cyclic presence of onshore glaciers and changes in ocean circulation. Middle Miocene transitions include rapid decreases in sedimentation rates, increased ice-rafted debris, shifts in clays and other minerals, and regional erosion of the slope and rise. These transitions may reflect enhanced glacial erosion and reduced glacial meltwater from progressively colder ice. At this time, seismic data show that depocenters began to shift from the outer continental rise to the base of the continental slope coincident with the initial stages of the glacial erosion and overdeepening of the continental shelf. During the late Miocene to early Pliocene there was a transition to greater subglacial activity on the shelf and more pronounced cyclic facies variations on the continental rise. At this time, severe glacial morphologies initiated on the shelf with the erosion of Prydz Channel and other troughs by fast-moving ice and the deposition of overcompacted glacial diamictons by slow-moving ice on adjacent banks. The Prydz trough-mouth fan also began to form with alternating deposition of debris flows (ice at shelf edge) and muddy units (reduced ice) (Site 1167). The fan also records a transition during the late Pleistocene for times younger than 780 k.y. when short-term glacial variations continued but ice reached the shelf edge only a few times. Both short-term and long-term transitions characterize the Cenozoic evolution of the Prydz Bay region from the Cretaceous nonglacial to late Neogene full-glacial paleoenvironments. These transitions are known only from ODP cores, and further insights will require additional drilling.

Prydz Bay region↗
USGS1989

Organic matter at sites 642, 643, and 644, ODP Leg 104

Sedimentary extractable organic matter was analyzed at three ODP Leg 104 sites in the Norwegian Sea. Organic carbon content ranged from less than 0.1% to a maximum of 1.8%. Extractable organic matter content and unresolved complex mixture concentrations were low and randomly distributed. Low levels of aliphatic (branched and normal) and aromatic hydrocarbons were detected in all of the sediments analyzed. Total aliphatic and aromatic hydrocarbon concentrations ranged from 176 to 3,214 and 6 to 820 ppb, respectively. The concentrations of individual aliphatic (n-C15 to n-C32) and aromatic (two- to five-ring) hydrocarbons were generally less than 50 ppb and less than 10 ppb, respectively. No significant trend with sub-bottom depth was observed in either bulk organic matter or individual hydrocarbon concentrations. The predominant source of Cenozoic sedimentary hydrocarbons is concluded to be ice-rafted debris from the adjacent continent. All sites contain a mixture of recycled, mature petroleum-related and terrestrially derived hydrocarbons.

Proceedings of the Ocean Drilling Program: Scienti↗
USGS1989

Hydrocarbon gases in sediment of the Voring Plateau, Norwegian Sea

Geochemical studies at three ODP Leg 104 sites on the Wring Plateau help define the distribution of hydrocarbon gases in sediment of this prominent feature of the Norwegian continental margin. Low levels of hydrocarbon gas were encountered in sediment of the outer part of the plateau, but sediment of the inner part of the plateau is very gassy. The molecular composition of inner plateau gases ( > 99.9% methane) and the carbon isotopic composition of the methane (avg. = - 76%o relative to the PDB standard) clearly show that the gas is biogenic. Heavier hydrocarbon gases accompany this methane, and their presence is probably a result of both chemical and microbial low-temperature diagenesis. Although these heavier hydrocarbons were not detected in sediment of the outer part of the plateau during shipboard analyses, subsequent shore-based analyses showed that these compounds are present at very low concentrations. Methane in the gassy sediment of the inner part of the plateau may be present as gas hydrates, judging from sedimentological and inorganic geochemical considerations, but no discernible gas hydrates were recovered during drilling.

Proceedings of the Ocean Drilling Program: Scienti↗
USGS1989

Organic geochemistry on Leg 104

The Leg 104 organic geochemistry program consisted of monitoring (a) hydrocarbon gases, (b) organic and inorganic carbon, and (c) parameters resulting from Rock-Eval pyrolysis at three sites on the Vdring Plateau. The results amplify some of those obtained earlier on Deep Sea Drilling Project (DSDP) Leg 38. In a regional sense there is an inverse correlation between amounts of hydrocarbon gas and organic carbon. For example, significant concentrations of methane are present only at Site 644 in the inner part of the plateau where organic carbon contents are always less than 1%; in contrast, at Site 642 on the outer plateau, methane concentrations are very low (ppm range) whereas amounts of organic carbon approach 2%. Only at Site 644 are the environmental conditions such that methanogenesis is an active diagenetic process. Because of the importance of routine gas analyses to the Ocean Drilling Program (ODP), a procedure was devised to improve the use of Vacutainers for collection of gas samples. Comparison of methods for determining organic carbon showed that at Sites 643 and 644 Rock-Eval TOC could be used as a measure of organic carbon, but not at Site 642. Although no liquid or solid hydrocarbons were encountered at any of the sites, a catalog of potential organic geochemical contaminants was developed in anticipation of such a discovery.

Proceedings of the Ocean Drilling Program: Scienti↗
USGS1989

Geochemical expression of early diagenesis in middle Eocene-lower Oligocene pelagic sediments in the southern Labrador Sea, Site 647, ODP Leg 105

Geochemical analyses of the middle Eocene through lower Oligocene lithologic Unit IIIC (260-518 meters below sea floor [mbsf]) indicate a relatively constant geochemical composition of the detrital fraction throughout this depositional interval at Ocean Drilling Program (ODP) Site 647 in the southern Labrador Sea. The main variability occurs in redox-sensitive elements (e.g., iron, manganese, and phosphorus), which may be related to early diagenetic inability in anaerobic pore waters during bacterial decomposition of organic matter. Initial preservation of organic matter was mediated by high sedimentation rates (36 m/m.Y.). High iron (Fe) and manganese (Mn) contents are associated with carbonate concretions of siderite, manganosiderite, and rhodochrosite. These concretions probably formed in response to elevated pore-water alkalinity and total dissolved carbon dioxide (CO2) concentrations resulting from bacterial sulfate reduction, as indicated by nodule stable-isotope compositions and pore-water geochemistry. These nodules differ from those found in upper Cenozoic hemipelagic sequences in that they are not associated with methanogenesis. Phosphate minerals (carbonate-fluorapatite) precipitated in some intervals, probably as the result of desorption of phosphorus from iron and manganese during reduction. The bulk chemical composition of the sediments differs little from that of North Atlantic Quaternary abyssal red clays, but may contain a minor hydrothermal component. The silicon/ aluminum (Si/Al) ratio, however, is high and variable and probably reflects original variations in biagenic opal, much of which is now altered to smectite and/or opal CT. An increase in the sodium/potassium (Na/K) ratio in the upper Eocene corresponds to the beginning of coarser-grained feldspar flux to the site, possibly marking the onset of more vigorous deep currents. Although the Site 647 cores provide a nearly complete high-resolution, high-latitude Eocene-Oligocene record, the high sedimentation rate and somewhat unusual diagenetic conditions have led to variable alteration of benthic foraminifers and fine-fraction carbonate and have overprinted the original stable-isotope records. Planktonic foraminifers are less altered, but on the whole, there is little chance of sorting out the nature and timing of environmental change on the basis of our stable-isotope analyses.

Proceedings of the Ocean Drilling Program: Scienti↗
USGS1990

Diagenesis and interstitial-water chemistry at the Peruvian continental margin; major constituents and strontium isotopes

Two distinct hydrogeochemical regimes currently dominate the Peruvian continental margin. One, in shallower water (150-450 m) shelf to upper-slope regions, is characterized by interstitial waters with strong positive chloride gradients with depth. The maximum measured value of 1043 mM chloride at Site 680 at ITS corresponds to a degree of seawater evaporation of ~2 times. Major ion chemistry and strontioum isotopic composition of the interstitial waters suggest that a subsurface brine that has a marine origin and is of pre-early Miocene "age," profoundly influences the chemistry and diagenesis of this shelf environment. Site 684 at ~9°S must be closest to the source of this brine, which becomes diluted with seawater and/or interstitial water as it flows southward toward Site 686 at ~13°S (and probably beyond) at a rate of approximately 3 to 4 cm/yr, since early Miocene time. The other regime, in deep water (3000-5000 m) middle to lower-slope regions, is characterized by interstitial waters with steep negative and nonsteady-state chloride gradients with depth. The minimum measured value of 454 mM chloride, at Site 683 at ITS, corresponds to —20% dilution of seawater chloride The most probably sources of these low-chloride fluids are gas hydrate dissociation and mineral (particularly clay) dehydration reactions. Fluid advection is consistent with (1) the extent of dilution shown in the chloride profiles, (2) the striking nonsteady-state depth profiles of chlorides at Sites 683 and 688 and of 87Sr/86Sr ratios at Site 685, and (3) the temperatures resulting from an average geothermal gradient of 50°C/km and required for clay mineral dehydration reactions. Strontium isotope data reveal two separate fluid regimes in this slope region: a more northerly one at Sites 683 and 685 that is influenced by fluids with a radiogenic continental strontium signature, and a southerly one at Sites 682 and 688 that is influenced by fluids with a nonradiogenic oceanic signatures. Stratigraphically controlled fluid migration seems to prevail in this margin. Because of its special tectonic setting, Site 679 at ITS is geochemically distinct. The interstitial waters are characterized by seawater chloride concentrations to —200 mbsf and deeper by a significantly lower chloride concentration of about two-thirds of the value in seawater, suggesting mixing with a meteoric water source. Regardless of the hydrogeochemical regime, the chemistry and isotopic compositions of the interstitial waters at all sites are markedly modified by diagenesis, particularly by calcite and dolomite crystallization.

Peruvian Continental Margin↗
USGS1990

Hydrocarbon gases in Tertiary and Quaternary sediments offshore Peru; results and comparisons

Hydrocarbon gases (methane, ethane, propane, isobutane, «-butane, ethene, and propene) are present in Tertiary and Quaternary shelf, upper-slope, and lower-slope deposits of the Peruvian continental margin. Methane dominates the composition of the hydrocarbon gas at all 10 sites examined during Ocean Drilling Program (ODP) Leg 112. Generation of methane is regulated by the amount of sulfate in pore water. Wherever sulfate concentrations approach or equal zero, methane concentrations increase rapidly, reaching values near 100,000 /tL/L of wet sediment at eight of the 10 sites. Methane at all 10 sites results from methanogenesis, which is inhibited where sulfate is present and microbial reduction of sulfate occurs. Hydrocarbon gases heavier than methane also are present, but at much lower concentrations than methane. These hydrocarbons are thought to result from early thermal and microbial diagenesis, based on relative gas compositions and trends of concentrations with depth. With few exceptions, the results obtained in the shipboard and shore-based laboratories are comparable for methane and ethane in sediments of Leg 112. Reanalyses of canned sediments from ODP Leg 104 and from Deep Sea Drilling Project (DSDP) Legs 76 and 84 show that gas samples can be stored for as long as 8 yr, but the amounts of individual hydrocarbon gases retained vary. Nevertheless, the trends of the data sets with depth are similar for fresh and stored samples.

ODP Leg 112↗
USGS1990

Gas hydrates of the Peruvian outer continental margin

Gas hydrates were recovered during coring by Ocean Drilling Program (ODP) Leg 112 at Sites 685 and 688 on the Peruvian outer continental margin at latitudes of 9° and 11.5°S, where water depths are 5070 and 3820 m, respectively. In addition, nearby Sites 682 and 683 yielded compelling evidence that gas hydrates are present, but gas hydrates were not directly observed there. Anomalous acoustic reflectors, known as bottom-simulating reflectors (BSRs), on marine seismic profiles from the region also provided inferential evidence that gas hydrates are present. Geothermal gradients of about 43 and 49°C/km were calculated on the basis of relations between depths to BSRs, bottom-water temperatures, and the pressure-temperature stability field of gas hydrates. Geochemical studies revealed that methane concentrations increase rapidly with depth after pore-water sulfate concentrations have been depleted. The relationship between methane and sulfate suggests that microbial processes account for the generation of methane, and the relationship between the carbon isotopic composition of methane and dissolved carbon dioxide supports this suggestion. We believe that decreasing chlorinity in pore water from squeezed sediment at the four sites results mainly from the decomposition of gas hydrates and is a dilution artifact observed as a result of the squeezing procedure. Maximum chlorinity values at or near the surface result from excess salt that comes from the formation of gas hydrates composed of freshwater. Record alkalinity attests to the intensity of diagenetic processes and has significant effects on salinity profiles at these sites. Gas hydrates were recovered at 99 and 166 meters below the seafloor (mbsf) at Site 685, and at 141 mbsf at Site 688 in Pleistocene diatomaceous mud. Methane constitutes more than 99% of the hydrocarbon gas mixture in the gas hydrates. The volumetric ratio of methane to water in the sample from Site 685 is 100, indicating that the sampled gas hydrate is either undersaturated with respect to methane or had partially decomposed during core recovery or both. The discovery of gas hydrates in lower slope deposits of the Peruvian outer continental margin extends our knowledge of gas-hydrate formation and occurrence in the Circum-Pacific region.

ODP Leg 112↗
USGS1990

Consolidation, triaxial shear-strength, and index-property characteristics of organic-rich sediment from the Peru continental margin: Results from Leg 112

Sites 679, 680, and 681 of the Ocean Drilling Program were drilled along an east-west transect across an organic-rich, diatomaceous, coastal upwelling facies that occurs as a shelf/slope lens along the Peru continental margin. Seven 60-cm-long, unsplit core sections from these sites were tested for consolidation, triaxial shear strength, and geotechnical index properties. The testing showed that the sediment has unusually high water content, Atterberg limits, degree of overconsolidation, compressibility, and shear strength. The sediment has unusually low density and grain specific gravity. Atterberg limits, grain specific gravity, compressibility, and apparent excess maximum past stress increase linearly with organic-carbon content, which also correlates positively with diatom content. Overconsolidation measured in these tests is probably not a result of sediment erosion or slumping, but rather the result of diagenesis or interparticle bonding by organic matter. High shear strengths were measured throughout, but particularly high relative shear strengths (as indicated by friction angles and degrees of dilatancy during shear) occur near 20 mbsf. This "crustlike" behavior is probably produced by early diagenesis (perhaps including dolotomization) within the upper 20 m, and is complemented by interlocking of diatoms.

Proceedings of the Ocean Drilling Program: Scienti↗
USGS1990

Hydrocarbons in sediment of the Weddell Sea, Antarctica

Heavy hydrocarbons (about C15+) are ubiquitous but minor components in sediment from three sites (692, 693, and 694) drilled during Ocean Drilling Program (ODP) Leg 113. This preliminary report is the first to describe the distribution of some of these hydrocarbons in sediment of the Weddell Sea. Samples from Sites 692 and 693, located on a mid-slope bench along the margin of Queen Maud Land, span a time interval from Early Cretaceous to Pleistocene. In samples from the Tertiary portion of the record, having an average organic-carbon content of about 0.2%, n-alkanes are common and are characterized by populations that indicate both marine and terrigenous sources. In contrast, samples from the Cretaceous portion of the record, having an average organic carbon content of about 4%, contain mixtures of hydrocarbons in which n-alkanes are secondary in abundance to the isoprenoid hydrocarbons, pristane and phytane. Diasterenes, sterenes, and hopenes are present in anomalously high concentrations and indicate immaturity. The Cretaceous hydrocarbons appear to be mainly primary, whereas the Tertiary hydrocarbons contain compounds which indicate that the sediment, along with its organic content, has been recycled. Samples from Site 694, located in the Weddell Sea on the abyssal plain, range in age from late Miocene to early Pliocene.

Proceedings of the Ocean Drilling Program: Scienti↗