834 resultados para Lipid-core Peptide System


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Bedding dips in the CRP-3 drillhole were determined in three ways: (1) analysis of a dipmeter log, (2) identification of bed boundaries on borehole televiewer log images, and (3) identification of bed boundaries on digital images of the outer surfaces of oriented cores. All three methods determine both dip magnitude and downdip azimuth of bedding. Dipmeter results document variations in bedding dip throughout the logged interval (20-902 mbsf), whereas core and televiewer results are available at present only for selected depth intervals. Dipmeter data indicate that structural dip is remarkably constant, at 21° dip to azimuth 65°, throughout the Tertiary shelf section, except for the top 100 m where dips appear to be 5-10° shallower. This pattern, in conjunction with the systematically increasing dips throughout CRP-2A, suggests that the growth faulting active during CRP-2A deposition began during the final period of deposition at CRP-3. Normal faults at 260 and 539 mbsf in CRP-3 exhibit neither drag (localized dip steepening) nor significant changes in structural dip across them. Oriented core and televiewer analyses, covering a total of 200 m in the interval 400-900 mbsf, indicate bedding patterns that confirm the dipmeter results. The doleritic breccia at the base of the Tertiary section has steeper dips than overlying structural dips, possibly indicating a sedimentary dip to ENE in these fan sediments. Dip directions in the underlying Devonian Beacon sandstone are surprisingly similar to those in the overlying Tertiary section. Superimposed on the average Beacon dip of 22° to the ENE are localized tilts of up to 20°, probably caused by Tertiary fracturing and brecciation rather than original sedimentary dip variations.

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Sparse to moderately abundant foraminiferal assemblages from Oligocene and Lower Miocene sediments in the CRP-2/2A drillhole contain C.27 genera and 42 species of calcareous benthic foraminifera. No planktic or agglutinated taxa were observed. On the basis of their faunal characteristics, four Foraminiferal Units are defined in drillhole succession: Foraminiferal Unit I (26.91-193.95 mbsf), mostly sparse assemblages with Elphidium magellanicum and Cribroelphidium sp.; Foraminiferal Unit II (193.95-342.42 mbsf), mostly moderately abundant assemblages with Cassidulinoides aequilatera and Eponides bradyi; Foraminiferal Unit III (342.42-486.19 mbsf), moderately abundant to sparse assemblages characterised by Cassidulinoides chapmani and Stainforthia sp.; and Foraminiferal Unit IV, Improverished (486.19-624.15, total depth, mbsf), with mostly barren residues, but with large Milioliidae recorded in situ at various horizons in the drill core. Foraminiferal Units I-IV lack taxa allowing correlation to standard zonal schemes. Inspection of faunal records from CIROS-1 and DSDP 270 indicates that, although the faunas show an overall similarity, CRP-2/2A Foraminiferal Units I-IV are not identifiable at these sites. The units are therefore most likely to reflect local environmental changes, and probably will prove useful for local correlation, but their lateral extent is undetermined. All four assemblages apparently represent various glacially-influenced shelf environments, and appear to reflect a long term deepening trend from Units IV to II, from perhaps inner to mid or outer-shelf depths, followed by a return to shallower, inner shelf, conditios for Unit I.

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Sediment deformation features in CRP-2/2A were described during normal logging procedures and from core-scan images. In this paper the origin of soft-sediment folding, contorted bedding, microfaulting, clastic dykes, shear zones and intraformational breccias is discussed. The features have a stratigraphic distribution related to major unconformities and sequence boundaries. Hypotheses for the origins of sediment deformation include hydrofracturing, subglacial shearing, slumping, and gas hydrate formation. Shear zones, microfaults, clastic dykes and contorted bedding within rapidly deposited sediments, suggest that slumping in an ice-distal environment occurred in the early Oligocene. A till wedge beneath a diamictite at 364 mbsf the mid-Oligocene section represents the oldest evidence of grounded ice in CRP-2/2A. Shear zones with a subglacial origin in the early late Oligocene and early Miocene sections of the core are evidence of further grounding events. The interpretation of sediment deformation in CRP-2/2A is compared to other Antarctic stratigraphic records and global eustatic change between the late Eocenel/early Oligocene and the middle Miocene.

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Strontium isotope stratigraphy was used to date 5 discrete horizons within the CRP-3 drillhole. A single in situ modiolid bivalve fragment at 10.88 mbsf gives an age of 30.9 (±0.8) Ma for the associated sediment. The four remaining well preserved fragments recovered from 29.94-190.31 mbsf are within error of this age, indicating a high sedimentation rate and suggesting little time is missing in disconformities. The diagenetic alteration of carbonate macrofossils by continental fluids (and possibly seawater) is a common feature to 320 mbsf.

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This PhD thesis focused on the analysis and application of microbial membrane lipids as biomarkers in marine sediments. Existing protocols for lipid extraction from marine sediments and biomass were modified. In addition, recent protocols based on high-performance liquid chromatography coupled to mass spectrometry (HPLC-MS) as well as state-of-the-art mass spectrometric analysis by quadrupole time-of-flight (MSqTOF) and the triple quadrupole (MSQQQ) mass spectrometer were used to investigate matrix effects and evaluate the reliability of quantitative analysis in marine environmental samples. The improved lipid extraction and quantification were used to analyze Black Sea water column and sediments samples to a depth of 8 meters from site GeoB 15105 taken during cruise M84/1 (DARCSEAS) with R/V Meteor to apply lipid analysis in benthic bio systems. With this component specific differentiation between planktonic and benthic lipid signature we assessed possible lipid sources. Here, this high detail lipid fingerprinting allowed us to observe changes in the head group and lipid core structures of the intact polar lipids according to the geochemical zonation.

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Seven hundred and nineteen samples from throughout the Cainozoic section in CRP-3 were analysed by a Malvern Mastersizes laser particle analyser, in order to derive a stratigraphic distribution of grain-size parameters downhole. Entropy analysis of these data (using the method of Woolfe & Michibayashi, 1995) allowed recognition of four groups of samples, each group characterised by a distinctive grain-size distribution. Group 1, which shows a multi-modal distribution, corresponds to mudrocks, interbedded mudrock/sandstone facies, muddy sandstones and diamictites. Group 2, with a sand-grade mode but showing wide dispersion of particle size, corresponds to muddy sandstones, a few cleaner sandstones and some conglomerates. Group 3 and Group 4 are also sand-dominated, with better grain-size sorting, and correspond to clean, well-washed sandstones of varying mean grain-size (medium and fine modes, respectively). The downhole disappearance of Group 1, and dominance of Groups 3 and 4 reflect a concomitant change from mudrock- and diamictite-rich lithology to a section dominated by clean, well-washed sandstones with minor conglomerates. Progressive downhole increases in percentage sand and principal mode also reflect these changes. Significant shifts in grain-size parameters and entropy group membership were noted across sequence boundaries and seismic reflectors, as recognised in other studies.