Models of aggradation versus progradation in the Himalayan Foreland   总被引：1，自引：0，他引：1  

Douglas W. Burbank  Richard A. Beck 《International Journal of Earth Sciences》1991,80(3):623-638

A frequent goal of decompaction analysis is to reconstruct histories of basin subsidence and tectonic loading. In marine environments, eustatic and paleobathymetric uncertainties limit the resolution of these reconstructions. Whereas in the terrestrial basins, these ambiguities are absent, it is still necessary to account for depositional slopes between localities in order to analyze three-dimensional patterns of subsidence. We define two end-members for depositional surfaces: aggradation and progradation. The relative importance of either end-member is a function of the interplay between the rate of net sediment accumulation and the rate of basin subsidence. The models predict the patterns of major drainages (transverse versus longitudinal) and the way in which provenance should be reflected within different portions of a basin. Consequently, paleocurrent and provenance data from the ancient stratigraphic record can be used to distinguish between these endmembers. The subhorizontal depositional surfaces that dominate during times of aggradation provide a well defined reference frame for regional analysis of decompacted stratigraphies and related subsidence. Depositional slopes during progradation can not be as precisely specified, and consequently yield greater uncertainties in reconstructions of subsidence. These models are applied to the Mio-Pliocene foreland basin of the northwestern Himalaya, where sequences of isochronous strata have been analyzed throughout the basin. These time-controlled data delineate a distinctive evolution from largely aggradational to largely progradational depositional geometries as deformation progressively encroaches on the foreland. Such a reconstruction of past depositional surfaces provides a well constrained reference frame for subsequent integration of subsidence histories from throughout the foreland.

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Zusammenfassung Ein häufiges Ziel der Dekompaktionsanalyse ist es die Beckenabsenkung und die tektonische Belastung zu rekonstruieren. In marinen Ablagerungsräumen limitieren eustatische und paläobathymetrische Unsicherheiten die Auflösung der Rekonstruktion. Bei terrestrischen Becken fehlen diese Zweideutigkeiten; es ist aber trotzdem notwendig, Rechenschaft über den Ablagerungshang zwischen verschiedenen Lokalitäten abzulegen, um dreidimensionale Subsidenzmuster zu analysieren. Wir definieren zwei Endglieder von Ablagerangsflächen: Aggradation und Progradation. Die relative Wichtigkeit des jeweiligen Endglieds ist eine Funktion des Zusammenspiels zwischen der Nettorate der Sedimentakkumulation und der Beckensubsidenz. Die Modelle sagen die Hauptentwässerungsmuster (quer- oder längsverlaufend) vorher, sowie den Weg in dem die Sedimentherkunft innerhalb verschiedener Bereiche des Beckens berücksichtigt werden sollte. Folglich können Paläoströmungs- und Herkunftsdaten alter stratigraphischer Überlieferungen benutzt werden, um zwischen den Endgliedern zu unterscheiden. Die subhorizontale Ablagerungsfläche welche zur Zeit der Aggradation dominant ist, liefert einen gut definierten Referenzrahmen für die regionale Analyse von dekomprimierten Formationen und der damit verknüpften Subsidenz. Ablagerangshänge während Progradation können nicht präzise spezifiziert werden und beinhalten daher größere Unsicherheiten bei der Rekonstruktion der Subsidenz. Diese Modelle wurden übertragen auf das miozäne bis pliozäne Vorgebirgsbecken des nordwestlichen Himalayas, wo Sequenzen von isochronen Schichten durch das gesamte Becken analysiert werden konnten. Diese zeitkontrollierten Daten schildern eine ganz bestimmte Entwicklung, die von einer hauptsächlich aggradierenden zu einer progradierenden Ablagerangsgeometrie verlief, während der die Deformation schrittweise in Richtung Vorland übergriff. Diese Rekonstruktion von ehemaligen Ablagerangsflächen liefert einen guten Referenzrahmen für die folgende Integration der Subsidenzgeschichte des gesamten Vorlands.

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Résumé L'analyse de décompaction a souvent pour but de reconstituer l'histoire de la subsidence d'un bassin et de la charge tectonique. Dans les milieux marins, de telles reconstitutions sont limitées par des incertitudes de caractère eustatique et paléobathymétrique. Par contre, ces ambiguïtés ne se présentent pas dans le cas des bassins continentaux, où il convient néanmoins de tenir compte de la pente de la surface de dépôt entre les divers points considérés pour établir un schéma tridimensionnel de la subsidence. Nous définissons deux situations extrêmes pour les surfaces de dépôt: l'aggradation et la progradation. L'importance relative de ces deux extrêmes est fonction de l'interaction entre le taux d'accumulation net des sédiments et le taux de subsidence du bassin. Les modèles prévoient la répartition des drainages principaux (transverse ou longitudinal) et la manière dont l'origine des sédiments peut se répercuter dans les diverses parties d'un bassin. Il en résulte que des informations fournies par les relevés stratigraphiques à propos des paléocourants et de la source des sédiments peuvent être utilisées pour faire la distinction entre les deux cas extrêmes. Les surfaces de dépôt subhorizontales, qui prédominent pendant les périodes d'aggradation, fournissent un bon cadre de référence pour les analyses régionales de formations décompactées et de la subsidence qui leur est associée. Les surfaces de dépôt inclinées qui se présentent au cours des progradations ne peuvent pas être définies de manière aussi précise et engendrent par conséquent plus d'incertitude dans la reconstitution de la subsidence. Les auteurs appliquent ces modèles au bassin mio-pliocène d'avant-pays de l'Himalaya nord-occidental, dans lequel des séquences de couches isochrones ont été suivies à travers tout le bassin. Ces données, chronologiquement définies, fournissent l'image d'une évolution nette, depuis des géométries typiques d'aggradation jusqu' à des géométries typiques de progradation, au fur et à mesure de l'emprise progressive de la déformation sur l'avant-pays. Une telle reconstitution des surfaces de dépôt anciennes fournit un bon cadre de référence en vue de l'intégration ultérieure de l'histoire de la subsidence dans l'ensemble de l'avant-pays.

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V792 Her=HD 155638: A totally eclipsing RS CVn binary     

Charles H. Nelson  Douglas S. Hall  Francis C. Fekel  Robert E. Fried  Richard E. Lines  Helen C. Lines 《Astrophysics and Space Science》1991,182(1):1-17

Photometry of HD 155638=V792 Her has been analyzed to determine the elements of this totally eclipsing RS CVn binary. The light variation outside eclipse was found to have a period of 27^d.07±0^d.07, which is slightly different from the 27^d.5384±0^d.0045 orbital period. Analysis of the eclipses was achieved by a modification of the Russell-Merrill technique. With the aid of radial velocity measures, absolute elements were obtained for the hot and cool stars, respectively;R _h=2.58R ,R _c=12.28R ,M _h=1.40M ,M _c=1.46M ,i=80^o.61 and velocity semi-amplitudesK _c=48.36 km s^–1±0.79 km s^–1, andK _h=50.50 km s^–1±0.33 km s^–1. The apparent magnitudes areV _h=9 ^m .73 andV _c=8 ^m .48. The distance to HD 155638 was estimated to be 310 parsecs.  相似文献   

Archean high-Mg monzodiorite–syenite,epidote skarn,and biotite–sericite gold lodes in the Granny Smith–Wallaby district,Australia: U–Pb and Re–Os chronometry of two intrusion-related hydrothermal systems     

Andreas G. Mueller  Gregory C. Hall  Alexander A. Nemchin  Holly J. Stein  Robert A. Creaser  Douglas R. Mason 《Mineralium Deposita》2008,43(3):337-362

The Granny Smith (37 t Au production) and Wallaby deposits (38 t out of a 180 t Au resource) are located northeast of Kalgoorlie, in 2.7 Ga greenstones of the Eastern Goldfields Province, the youngest orogenic belt of the Yilgarn craton, Western Australia. At Granny Smith, a zoned monzodiorite–granodiorite stock, dated by a concordant titanite–zircon U–Pb age of 2,665 ± 3 Ma, cuts across east-dipping thrust faults. The stock is fractured but not displaced and sets a minimum age for large-scale (1 km) thrust faulting (D2), regional folding (D1), and dynamothermal metamorphism in the mining district. The local gold–pyrite mineralization, controlled by fractured fault zones, is younger than 2,665 ± 3 Ma. In augite–hornblende monzodiorite, alteration progressed from a hematite-stained alkali feldspar–quartz–calcite assemblage and quartz–molybdenite–pyrite veins to a late reduced sericite–dolomite–albite assemblage. Gold-related monazite and xenotime define a U–Pb age of 2,660 ± 5 Ma, and molybdenite from veins a Re–Os isochron age of 2,661 ± 6 Ma, indicating that mineralization took place shortly after the emplacement of the main stock, perhaps coincident with the intrusion of late alkali granite dikes. At Wallaby, a NE-trending swarm of porphyry dikes comprising augite monzonite, monzodiorite, and minor kersantite intrudes folded and thrust-faulted molasse. The conglomerate and the dikes are overprinted by barren (<0.01 g/t Au) anhydrite-bearing epidote–actinolite–calcite skarn, forming a 600-m-wide and >1,600-m-long replacement pipe, which is intruded by a younger ring dike of syenite porphyry pervasively altered to muscovite + calcite + pyrite. Skarn and syenite are cut by pink biotite–calcite veins, containing magnetite + pyrite and subeconomic gold–silver mineralization (Au/Ag = 0.2). The veins are associated with red biotite–sericite–calcite–albite alteration in adjacent monzonite dikes. Structural relations and the concordant titanite U–Pb age of the skarn constrain intrusion-related mineralization to 2,662 ± 3 Ma. The main-stage gold–pyrite ore (Au/Ag >10) forms hematite-stained sericite–dolomite–albite lodes in stacked D2 reverse faults, which offset skarn, syenite, and the biotite–calcite veins by up to 25 m. The molybdenite Re–Os age (2,661 ± 10 Ma) of the ore suggests a genetic link to intrusive activity but is in apparent conflict with a monazite–xenotime U–Pb age (2,651 ± 6 Ma), which differs from that of the skarn at the 95% confidence level. The time relationships at both gold deposits are inconsistent with orogenic models invoking a principal role for metamorphic fluids released during the main phase of compression in the fold belt. Instead, mineralization is related in space and time to late-orogenic, magnetite-series, high-Mg monzodiorite–syenite intrusions of mantle origin, characterized by Mg/(Mg + Fe_TOTAL) = 0.31–0.57, high Cr (34–96 ppm), Ni (22–63 ppm), Ba (1,056–2,321 ppm), Sr (1,268–2,457 ppm), Th (15–36 ppm), and rare earth elements (total REE: 343–523 ppm). At Wallaby, shared Ca–K–CO₂ metasomatism and Th-REE enrichment (in allanite) link Au–Ag mineralization in biotite–calcite veins to the formation of the giant epidote skarn, implicating a Th + REE-rich syenite pluton at depth as the source of the oxidized hydrothermal fluid. At Granny Smith, lead isotope data and the Rb–Th–U signature of early hematite-bearing wall-rock alteration point to fluid released by the source pluton of the differentiated alkali granite dikes.  相似文献   

Oxidation of pyrite during extraction of carbonate associated sulfate     

Pedro J. Marenco  Frank A. Corsetti  Douglas E. Hammond  Alan J. Kaufman  David J. Bottjer 《Chemical Geology》2008,247(1-2):124-132

The sulfur isotopic composition of carbonate associated sulfate (CAS) has been used to investigate the geochemistry of ancient seawater sulfate. However, few studies have quantified the reliability of δ³⁴S of CAS as a seawater sulfate proxy, especially with respect to later diagenetic overprinting. Pyrite, which typically has depleted δ³⁴S values due to authigenic fractionation associated with bacterial sulfate reduction, is a common constituent of marine sedimentary rocks. The oxidation of pyrite, whether during diagenesis or sample preparation, could thus adversely influence the sulfur isotopic composition of CAS. Here, we report the results of CAS extractions using HCl and acetic acid with samples spiked with varying amounts of pyrite. The results show a very strong linear relationship between the abundance of fine-grained pyrite added to the sample and the resultant abundance and δ³⁴S value of CAS. This data represents the first unequivocal evidence that pyrite is oxidized during the CAS extraction process. Our mixing models indicate that in samples with much less than 1 wt.% pyrite and relatively high δ³⁴S_pyrite values, the isotopic offset imparted by oxidation of pyrite should be much less than ? 4‰. A wealth of literature exists on the oxidation of pyrite by Fe³⁺ and we believe this mechanism drives the oxidation of pyrite during CAS extraction, during which the oxygen used to form sulfate is taken from H₂O, not O₂. Consequently, extracting CAS under anaerobic conditions would only slow, but not halt, the oxidation of pyrite. Future studies of CAS should attempt to quantify pyrite abundance and isotopic composition.  相似文献   

Quadruple sulfur isotope analysis of ca. 3.5 Ga Dresser Formation: New evidence for microbial sulfate reduction in the early Archean     

Yuichiro Ueno  Shuhei Ono  Douglas Rumble 《Geochimica et cosmochimica acta》2008,72(23):5675-5691

Multiple sulfur isotope system is a powerful new tracer for atmospheric, volcanic, and biological influences on sulfur cycles in the anoxic early Earth. Here, we report high-precision quadruple sulfur isotope analyses (³²S/³³S/³⁴S/³⁶S) of barite, pyrite in barite, and sulfides in related hydrothermal and igneous rocks occurring in the ca. 3.5 Ga Dresser Formation, Western Australia. Our results indicate that observed isotopic variations are mainly controlled by mixing of mass-dependently (MD) and non-mass-dependently fractionated (non-MD) sulfur reservoirs. Based on the quadruple sulfur isotope systematics (δ³⁴S-Δ³³S-Δ³⁶S) for these minerals, four end-member sulfur reservoirs have been recognized: (1) non-MD sulfate (δ³⁴S = −5 ± 2‰; Δ³³S = −3 ± 1‰); (2) MD sulfate (δ³⁴S = +10 ± 3‰); (3) non-MD sulfur (δ³⁴S > +6‰; Δ³³S > +4‰); and (4) igneous MD sulfur (δ³⁴S = Δ³³S = 0‰). The first and third components show a clear non-MD signatures, thus probably represent sulfate and sulfur aerosol inputs. The MD sulfate component (2) is enriched in ³⁴S (+10 ± 3‰) and may have originated from microbial and/or abiotic disproportionation of volcanic S or SO₂. Our results reconfirm that the Dresser barites contain small amounts of pyrite depleted in ³⁴S by 15-22‰ relative to the host barite. These barite-pyrite pairs exhibit a mass-dependent relationship of δ³³S/δ³⁴S with slope less than 0.512, which is consistent with that expected for microbial sulfate reduction and is significantly different from that of equilibrium fractionation (0.515). The barite-pyrite pairs also show up to 1‰ difference in Δ³⁶S values and steep Δ³⁶S/Δ³³S slopes, which deviate from the main Archean array (Δ³⁶S/Δ³³S = −0.9) and are comparable to isotope effects exhibited by sulfate reducing microbes (Δ³⁶S/Δ³³S = −5 to −11). These new lines of evidence support the existence of sulfate reducers at ca. 3.5 Ga, whereas microbial sulfur disproportionation may have been more limited than recently suggested.  相似文献   

SOME INTRODUCTORY NOTES ON REGIONAL DIVISION AND SET THEORY     

Reginald G. Golledge  Douglas M. Amadeo 《The Professional geographer》1966,18(1):14-19

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Magnitude-frequency relationship of coastal sand delivery by a southern California stream     

Douglas W. Stow  Howard H. Chang 《Geo-Marine Letters》1987,7(4):217-222

Coastal sand delivery by a stream in southern California is estimated based on a numerical model which stimulates unsteady flow, sediment transport, and the associated channel adjustments for a stream-delta system. An average annual sediment yield of 51,400 m³/yr is estimated for the San Dieguito River, which drains a semiarid watershed controlled by dams. Of the total sand delivery by the stream, 20.5 percent is contributed from floods greater than the 100-year flood; 17.6 percent from those between the 50- and 100-year events; 28.4 percent from those between the 25- and 50 year floods; and 33.5 percent from those smaller than the 25-year flood.  相似文献   

Effects of organic pollutants on methanogenesis,sulfate reduction and carbon dioxide evolution in salt marsh sediments     

Ronald P. Kiene  Douglas G. Capone 《Marine environmental research》1984,13(2):141-160

Anaerobic salt marsh sediments were amended with a variety of organic pollutants and the effects on methanogenesis, sulfate reduction and carbon dioxide evolution were examined. Addition of 1000 μg g^?1 (dry weight sediment) Arochlor 1221, lindane, endrin, benzene and phenanthrene resulted in no significant effects on the activities studied. Methanogenesis was inhibited by 1000 μg g^?1toxaphene, PCP, chlordane, naphthalene, DDT, Kepone and heptachlor and by 100 μg g^?1 PCP and toxaphene. At 1000 μg g^?1 naphthalene and toxaphene and 100 μg g^?1 PCP, a period of initial inhibition of methanogenesis was followed by stimulation relative to controls. Arochlor 1254 (1000 μg g^?1) and Temik (500 and 10 μg g^?1) stimulated methanogenesis from the outset. Temik at 500 μg g^?1 gave the greatest stimulation of methanogenesis (900% of controls) of any of the compounds studied. Sulfate reduction was inhibited by 1000 μg g^?1 PCP, toxaphene, naphthalene and chlordane and by 500 μg g^?1 atrazine and 100 μg g^?1 heptachlor. Sustained inhibition of sulfate reduction by naphthalene, toxaphene and PCP may have contributed to the stimulation of methanogenesis. Carbon dioxide evolution was not significantly affected by most of the compounds studied except for 100 μg g^?1 PCP and 1000 μg g^?1 aphthalene, each of which gave significant inhibition in only one of three experiments.Concentrations of individual organic pollutants required to cause observable effects were high. It is concluded that, except for highly polluted sediments, methanogenesis, sulfate reduction and CO₂ evolution would not be affected by the compounds studied here at concentrations typically found in the environment.  相似文献   

The dissociation constants of carbonic acid in seawater at salinities 5 to 45 and temperatures 0 to 45°C     

Rabindra N Roy  Lakshimi N Roy  Kathleen M Vogel  C Porter-Moore  Tara Pearson  Catherine E Good  Frank J Millero  Douglas M Campbell 《Marine Chemistry》1993,44(2-4)

The pK₁^* and pK₂^* for the dissociation of carbonic acid in seawater have been determined from 0 to 45°C and S = 5 to 45. The values of pK₁^* have been determined from emf measurements for the cell: where X is the mole fraction of CO₂ in the gas. The values of pK₂^* have been determined from emf measurements on the cell: The results have been fitted to the equations: where T is the temperature in K, S is the salinity, and the standard deviations of the fits are σ = 0.0048 in lnK₁^* and σ = 0.0070 in lnK₂^*.Our new results are in good agreement at S = 35 (±0.002 in pK₁^*and ±0.005 in pK₂^*) from 0 to 45°C with the earlier results of Goyet and Poisson (1989). Since our measurements are more precise than the earlier measurements due to the use of the Pt, H₂|AgCl, Ag electrode system, we feel that our equations should be used to calculate the components of the carbonate system in seawater.  相似文献   

Characterization and molecular analysis of hepatic microsomal UDP-glucuronosyltransferases in the marine fish, Pleuronectes platessa     

Douglas J Clarke  Brian Burchell  Stephen George 《Marine environmental research》1988,24(1-4)

Here we report the results of the first molecular enzymological study of fish UDP-glucuronosyltransferase (UDPGT). UDPGT activities of plaice liver microsomes were greatest for planar phenols and there was low but measurable conjugation of bilirubin, testosterone and androsterone. A highly purified preparation was isolated which possessed activities towards 1-naphthol, bilirubin and testosterone, containing several molecular weight species of M_r 52–56 kDa. On immunoblot analysis these proteins cross-reacted with a polyspecific anti-rat UDPGT antibody, suggesting that a number of plaice UDPGT isoforms with epitopes in common with the corresponding rat enzymes had been purified.  相似文献