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971.
Hollander DJ Sinninghe Damste JS Hayes JM de Leeuw JW Huc AY 《Organic Geochemistry》1993,20(8):1253-1263
Contents of 13C in kerogens and carbonates in 21 samples from a core of the MAX borehole, Mulhouse Evaporite Basin, range from -27.3 to -23.5 and -3.7 to -1.8% vs PDB, respectively. Organic nitrogen in the same samples is enriched in 15N relative to atmospheric N2 by 12.2-15.7%. Hydrogen indices and delta values for kerogens vary systematically with facies, averaging 493 mg HC/g Corg and -25.7% in the most saline facies (dominated by inputs from aquatic sources) and 267 mg HC/g Corg and -23.7% in the least saline facies (50/50 aquatic/terrigenous). Values of delta were measured for individual aliphatic hydrocarbons from three samples representing three different organic facies. For all samples, terrigenous inputs were unusually rich in 13C, the estimated delta value for bulk terrigenous debris, apparently derived partly from CAM plants, being -22.5%. In the most saline facies, isotopic evidence indicates the mixing of 13C-depleted products of photosynthetic bacteria with 13C-enriched products of halotolerant eukaryotic algae. At lower salinities, a change in the producer community is marked by a decrease in the 13C content of algal lipids. The content of 13C in algal lipids increases in the least saline facies, due either to succession of different organisms or to decreased concentrations of dissolved CO2. 相似文献
972.
Detailed investigations of high latitude sequences recently collected by the Ocean Drilling Program (ODP) indicate that periods of rapid climate change often culminated in brief transient climates, with more extreme conditions than subsequent long term climates. Two examples of such events have been identified in the Paleogene; the first in latest Paleocene time in the middle of a warming trend that began several million years earlier: the second in earliest Oligocene time near the end of a Middle Eocene to Late Oligocene global cooling trend. Superimposed on the earlier event was a sudden and extreme warming of both high latitude sea surface and deep ocean waters. Imbedded in the latter transition was an abrupt decline in high latitude temperatures and the brief appearance of a full size continental ice-sheet on Antarctica. In both cases the climate extremes were not stable, lasting for less than a few hundred thousand years, indicating a temporary or transient climate state. Geochemical and sedimentological evidence suggest that both Paleogene climate events were accompanied by reorganizations in ocean circulation, and major perturbations in marine productivity and the global carbon cycle. The Paleocene-Eocene thermal maximum was marked by reduced oceanic turnover and decreases in global delta 13C and in marine productivity, while the Early Oligocene glacial maximum was accompanied by intensification of deep ocean circulation and elevated delta 13C and productivity. It has been suggested that sudden changes in climate and/or ocean circulation might occur as a result of gradual forcing as certain physical thresholds are exceeded. We investigate the possibility that sudden reorganizations in ocean and/or atmosphere circulation during these abrupt transitions generated short-term positive feedbacks that briefly sustained these transient climatic states. 相似文献
973.
Adolf Kühnemann 《GeoJournal》1993,30(3):259-272
On the map of Europe, forming the south-western border region of Poland, is to be found the name Silesia, with in many cases its southern part emphasized — Upper Silesia. Any search for statistics as to its exact surface area and population size will be in vain. At the end of World War I, Upper Silesia found itself squeezed between two nationalistically-obsessed peoples, and economically too attractive to both to be allowed to play an idependent political role, as it had for centuries. Upper Silesia was in 1921 divided. After World War II, under the communist centralised power system, a completely colonial robber economy was pursued. Because of the coal production there is now here one of the greatest agglomeration areas in Europe, with an ageing heavy industry and a catastropihcally damaged environment. 相似文献
974.
P. F. Schofield C. M. B. Henderson S. A. T. Redfern G. van der Laan 《Physics and Chemistry of Minerals》1993,20(6):375-381
The solid solution sanmartinite (ZnWO4)—cuproscheelite (CuWO4) has been studied using Cu 2p X-ray absorption spectroscopy. While a single L3 absorption peak is observed for CuWO4, two distinct L3 absorption peaks with a separation of ~0.8 eV are observed for the intermediate samples in the solid solution. The two peaks represent distinct Cu sites: one with all CuO6 next nearest neighbours in the (Cu,Zn)O6 chains, another having at least one ZnO6 next nearest neighbour. Both sites show a linear increase in covalency as a function of increasing Cu-content. The relative intensities of the two absorption peaks is dependent upon the Cu-content and has been used to model the site occupancies. The results reveal that the local structural effects can be associated with a composition-dependent structural phase transition from P2/c (ZnWO4) to P $\bar 1$ (CuWO4). Deviations from a single-site model are explained in terms of the local environments, and evidence for site preferences and local clustering are explored. 相似文献
975.
A depth migration method is presented that uses Radon-transformed common-source seismograms as input. It is shown that the Radon depth migration method can be extended to spatially varying velocity depth models by using asymptotic ray theory (ART) to construct wavefield continuation operators. These operators downward continue an incident receiver-array plane wave and an assumed point-source wavefield into the subsurface. The migration velocity model is constrained to have longer characteristic wavelengths than the dominant source wavelength such that the ART approximations for the continuation operators are valid. This method is used successfully to migrate two synthetic data examples:
- 1 a point diffractor, and
- 2 a dipping layer and syncline interface model.
976.
Santschi Peter H. Honeyman Bruce D. Quigley Matthew S. 《Aquatic Sciences - Research Across Boundaries》1993,55(4):230-239
In 1975 Paul Schindler produced the first oceanic trace metal scavenging model to explicitly include the role of surface chemistry as a control on trace metal water column residence times. The eighteen years that have elapsed since the publication of Schindler's seminal paper have seen the development of a variety of oceanic scavenging models; yet, the fundamental insight of his Zero-order Model remains the benchmark. This paper describes the role of Paul Schindler's work on surface chemistry in providing a framework for the current generation of trace element scavenging models. 相似文献
977.
S. M. Eggins 《Contributions to Mineralogy and Petrology》1993,114(1):79-100
Key aspects of magma generation and magma evolution in subduction zones are addressed in a study of Ambae (Aoba) volcano, Vanuatu. Two major lava suites (a low-Ti suite and high-Ti suite) are recognised on the basis of phenocryst mineralogy, geochemistry, and stratigraphy. Phenocryst assemblages in the more primitive low-Ti suite are dominated by magnesian olivine (mg 80 to 93.4) and clinopyroxene (mg 80 to 92), and include accessory Cr-rich spinel (cr 50 to 84). Calcic plagioclase and titanomagnetite are important additional phenocryst phases in the high-Ti suite lavas and the most evolved low-Ti suite lavas. The low-Ti suite lavas span a continuous compositional range, from picritic (up to 20 wt% MgO) to high-alumina basalts (<5 wt% MgO), and are consistent with differentiation involving observed phenocrysts. Melt compositions (aphyric lavas and groundmasses) in the low-Ti suite form a liquid-line of descent which corresponds with the petrographically-determined order of crystallisation: olivine + Cr-spinel, followed by clinopyroxene + olivine + titanomagnetite, and then plagioclase + clinopyroxene + olivine + titanomagnetite. A primary melt for the low-Ti suite has been estimated by correcting the most magnesian melt composition (an aphyric lava with 10.5 wt% MgO) for crystal fractionation, at the oxidising conditions determined from olivine-spinel pairs (fo2 FMQ + 2.5 log units), until in equilibrium with the most magnesian olivine phenocrysts. The resultant composition has 15 wt% MgO and an mg
Fe2 value of 81. It requires deep (3 GPa) melting of the peridotitic mantle wedge at a potential temperature consistent with current estimates for the convecting upper mantle (T
p 1300°C). At least three geochemically-distinct source components are necessary to account for geochemical differences between, and geochemical heterogeneity within, the major lava suites. Two components, one LILE-rich and the other LILE- and LREE-rich, may both derive from the subducting ocean crust, possibly as an aqueous fluid and a silicate melt respeetively. A third component is attributed to either differnt degrees of melting, or extents of incompatible-element depletion, of the peridotitic mantle wedge. 相似文献
978.
I. A. Sigurdsson Dr. V. S. Kamenetsky Dr. A. J. Crawford Dr. S. M. Eggins Dr. S. K. Zlobin 《Mineralogy and Petrology》1993,47(2-4):149-169
Summary At its southernmost end, the main spreading centre of the North Fiji Basin is propagating into arc crust of the poorly-known Hunter Ridge. We define nine magmatic groups from major element glass chemistry and olivine and spinel compositions in samples dredged from twenty six sites in this area by the R/V Academician A. Nesmeyanov in 1990. These include groups of boninites, island arc tholeiites (IAT), mid-ocean ridge basalts (MORB), enriched mid-ocean ridge basalts (E-MORB), olivine porphyritic andesites and basaltic andesite and Na-rhyolites. Primitive lavas containing highly forsteritic olivine phenocrysts are common in all the groups, except for the rhyolites.We report over 100 glass analyses for dredged rocks from this region, and about 300 olivine-spinel pairs for representatives of all the magmatic groups identified, except the Na-rhyolites.The MORB in this region are probably produced at the propagating spreading centre in the southern part of the North Fiji Basin. Juxtaposition of shallow, hot MORB-source diapirs supplying the MORB in this area, and the sub-arc damp, refractory upper mantle beneath the Hunter Ridge, provides suitable petrogenetic conditions to produce a range of magma types, from island arc tholeiites through to high-Ca boninites. The latter were recovered in eleven dredges.The E-MORB lavas recovered from the extreme southern margin of the North Fiji Basin are shown to be essentially identical to those dredged from adjacent older South Fiji Basin crust. It is hypothesized that the former were either scraped off the South Fiji Basin crust during an episode of oblique subduction that may have generated the Hunter Ridge during the last 5 Myr, or alternatively, that slices of the South Fiji Basin crust were trapped and incorporated into the North Fiji Basin as the subduction zones fronting the Vanuatu arc stepped or propagated southward.
Primitive Inselbogen- und ozeanische Laven von Hunter Rücken und der Hunter BruchZone: die Bedeutung der Zusammensetzung von Glas, Olivin und Spinell
Zusammenfassung Das spreading centre des Nord-Fidschi-Beckens setzt sich an seinem südlichsten Ende in die Inselbogen-Kruste des noch wenig bekannten Hunter-Rückens fort.Wir definieren 9 magmatische Gruppen auf der Basis der Hauptelement-Zusammensetzung von Gläsern und der Zusammensetzung von Olivin und Spinell in Proben die das Forschungsschiff R/V Akademiker A. Nesmeyanov von 26 Stellen im Jahr 1990 aufgesammelt hat. Zu diesen gehören Gruppen von Boniniten, Inselbogentholeiiten (IAT), Basalten zentralozeanischer Rücken (MORB), angereicherte zentralozeanische Rücken (E-MORB), Olivin-porphyritische Andesite und basaltische Andesite, sowie Na-Rhyolite. Primitive Laven mit Olivinkristallen, die reich an Forsterit-Komponenten sind, kommen in allen diesen Gruppen, mit Ausnahme der Rhyolite, vor.Wir legen über 100 Glas-Analysen von Gesteinen aus diesem Gebiet vor und über 300 Olivin-Spinell-Paare für Vertreter aller der hier identifizierten magmatischen Gruppen, mit Ausnahme der Natriumrhyolite.Die MORB in diesem Gebiet sind wahrscheinlich an dem aktiven Spreading Center im Südteil des Nord-Fidschi-Beckens entstanden. Das nebeneinander Vorkommen von seichten heißen MORB-Quellen Diapiren, die MORB in diesem Gebiet erzeugen, und der Sub-Inselbogen, wasserhaltige, refraktäre obere Mantel unter dem Hunter Rücken führen zu geeigneten petrogenetischen Bedingungen für die Entstehung einer Vielfalt von Magmatypen, von Inselbogentholeiiten bis zu sehr Kalziumreichen Boniniten. Die letzteren wurden in 11 Dredge-Proben gefunden.Die E-MORS Laven, die aus dem extremen Südteil des Nord-Fidschi-Beckens entnommen wurden, sind im wesentlichen mit jenen identisch, die aus der benachbarten älteren Kruste des Süd-Fidschi-Beckens stammen. Es wird vermutet, daß die letzteren entweder aus dem Süd-Fidschi-Becken während einer Episode obliger Subduktion, die in den letzten 5 Millionen Jahren zur Entstehung des Hunter Ridge geführt hat, abgeschert wurden, oder auch daß Teile der Kruste des Süd-Fidschi-Beckens in das Nord-Fidschi-Becken inkorporiert wurden als Subduktionszonen gegenüber dem Vanuato-Bogen sich nach Süden fortbewegten.相似文献
979.
Summary The crystal structure of cesstibtantite has been solved from diffractometer data collected on samples from Leshaia, Russia and the Tanco pegmatite, Manitoba. Cesstibtantite from the Leshaia pegmatite (type locality) hasa 10.515(2) Å, space groupFd3m, composition Cs0.31(Sb0.57Na0.31Pb0.02Bi0.01)O.91(Ta1.88Nb0.12)2(O5.69[OH, F]0.31)6(OH, F)0.69, Z 8; its structure was refined toR 3.8,wR 4.3% using 96 observed (F > 3[F]) reflections (MoK). Cesstibtantite from the Tanco pegmatite hasa 10.496(1) Å, space groupFd3m, composition (Cs0.22K0.01)0.23(Na0.45Sb0.39Pb0.14· Ca0.06Bi0.02)1.06(Ta1.95Nb0.05)2(O5.78[OH,F]0.22)6(OH,F)0.55,Z 8; its structure was refined toR 3.9w R 3.7% using 104 observed reflections. Cesstibtantite differs from the normal pyrochlores in that it contains significant amounts of very large cations such as Cs. As these cations are too large (VIII[r] > 1.60 Å) for the conventional [8]-coordinated A site, they occupy the [18]-coordinated site, which normally contains monovalent anions. Natural cesstibtantite samples are non-ideal in that both Cs and monovalent anions occur at the site; thus cesstibtantite is intermediate to thenormal pyrochlores (with only monovalent anions at the site) and theinverse pyrochlores (with only large cations at the site).
Cesstibtantit—eine geologische Einfiihrung in die inversen Pyrochlore
Zusammenfassung Die Kristallstruktur von Cesstibtantit wurde auf der Basis von Diffraktometerdaten von Proben von Leshaia, Russland and dem Tanco Pegmatit, Manitoba, gelöst. Cesstibtantit aus dem Leshaia Pegmatit (Typlokalität) hat a 10.515(2) Å, RaumgruppeFd3m, die Zusammensetzung CS0.31(Sb0.57Na0.31Pb0.02Bi0.01)0.91(Ta1.88Nb0.12)2· (O5.69OH, F0.31)6(OH, F)0.69 Z 8; die Struktur wurde aufR 3.8,wR 4.3% verfeinert unter Benützung von 96 beobachteten Reflexen. Cesstibtantit vom Tanco Pegmatit hat a 10.496(1) Å, RaumgruppeFd3m, die Zusammensetzung (Cs0.22K0.01)0.23(Na0.45· Sb0.39Pb0.14Ca0.06Bi0.02)1.06(Ta1.95Nb0.05)2(O5.78OH,F0.22)6(OH,F)0.55,Z 8; seine Struktur wurde aufR 3.9wR 3.7% auf der Basis von 104 beobachteten Rettexen verfeinert. Cesstibtantit unterscheidet sich von normalen Pyrochloren insofern, als er signifikante Mengen von sehr großen Kationen, wie z.B. Cs enthält. Da these Kationen zu groß sind (VIII r 1.60 Å) für eine konventionelle [8]-koordinierteA Stelle, nehmen she die [18]-koordinierten Positionen ein, welche normalerweise monovalente Anionen enthalten. Natürliche Cesstibtantitproben sind nicht ideal insofern als sowohl Cs als auch monovalente Anionen in der Position vorkommen. Somit ist Cesstibtantit intermediär zu den normalen Pyrochloren (mit nur monovalenten Anionen auf der Position) and den inversen Pyrochloren (mit ausschließlichen großen Kationen an der Position).相似文献
980.
An occurrence of ardennite in quartz veins in piemontite schist,Western Otago,New Zealand 总被引:1,自引:0,他引:1
Summary Ardennite of complex composition: (Mn2+
3.488Ca0.509Ba0.002)=4(Mg0.916916 Fe3+
0.165 Mn3+
0.099Cu0.033Ni0.009Zn0.006 Ti0.008Al4.764)=6(As5+
0.823V5+
0.022P0.005B0.069Al0.042Si5.039)=6O21.81(OH)6.17 occurs in crack-seal quartz veins in quartz-albite-piemontite-spessartine-phengitehematite-chlorite-rutile-tourmaline ± calcite schist of the Haast Schist Group near Arrow Junction, western Otago, New Zealand. The Mn2+/Mn3+-ratio is sensitive to calculations and to accuracy of analyses. Boron is detected in ardennite for the first time. Other properties include = 1.734(3), = 1.735(3), = 1.751(3), 2VZ = 30(2)°;a = 8.721(1),b = 5.816(1),c = 18.545(3) Å,V = 940.7(2) Å3. Associated mineral phases are spessartine, hematite, piemontite containing 0.7% SrO and 0.06% PbO, and phengite. Later-stage vein minerals comprise chlorite, albite, and manganoan calcite which were deposited under less highly oxidizing conditions. Digenite with minor intergrown covellite occurs in small amount with manganoan calcite and quartz in a cross-cutting late-stage veina chalcopyrite and native copper occur in other late-stage veins. Arsenic and other components of the ardennite and associated minerals are derived from highly oxidized ferromanganese oxide- and hydroxide-bearing siliceous pelagic sediments that formed the protolith for the piemontite schist. The veins formed at a relatively early stage after metamorphism peaked in the chlorite zone of the greenschist facies under conditions that have been estimated at about 4.5 kbar, 390 °C.
With 4 Figures 相似文献
Vorkommen von Ardennit in Quarzgängen aus Piemontit-Schiefern, West-Otago, Neuseeland
Zusammenfassung Ardennit mit der Zusammensetzung (Mn2+ 3.488Ca0.509Ba0.002)=4(Mg0.916Fe3+ 0.165Mn3+ 0.099Cu0.033Ni0.009Zn0.006 Ti0.008Al4.764)=6(As5+ 0.823V5+ 0.022P0.005B0.069Al0.042Si5.039)=6O21.81(OH)6.17 tritt in Crack-seal-Quarzgängen in Quarz-Albit-Piemontit-Spessartin-Phengit-Hämatit-Chlorit-Rutil-Turmalin ± Calcit-Schiefern der Haast Schiefer-Gruppe nahe der Arrow Junction, West-Otago, Neuseeland, auf. Die Proportionen von Mn2+/Mn3+ hängen von der Kalkulation und der Genauigkeit der Analyse ab. Bor wird zum ersten Mal im Ardennit bestimmt. Andere Eigenschaften sind: = 1.734(3), = 1.735(3), = 1.751(3), 2Vz = 30(2)°; a = 8.721(1), b = 5.816(1), c = 18.545(3) Å, V = 940.7(2) Å3. Assoziierte Mineralphasen sind Spessartin, Hämatit, Piemontit, der 0.7% SrO und 0.06% PbO enthält und Phengit. Spät gebildete Gangmineralien, wie Chlorit, Albit und Mn-Calcit, sind unter geringer oxidierenden Bedingungen entstanden. Digenit mit etwas Covellin tritt in kleinen Mengen zusammen mit Mn-Calcit und Quartz in einem querschlägigen Gang auf, Chalcopyrit und gediegenes Kupfer kommen in anderen späten Gängen vor. Arsen und andere Komponenten des Ardennites and der assoziierten Minerale können von hochoxidierten, Fe-Mn-Oxid- und Hydroxyd-führenden, Sireichen, pelagischen Sedimenten hergeleitet werden, die das Ausgangsgestein für den Piemontit darstellen. Die Gänge wurden in einem relativ frühen Stadium, nach dem Metamorphosehöhepunkt, innerhalb der Chloritzone der Grünschiefer-Fazies, unter ungefähr 4.5 kbar und 390°C, gebildet.
With 4 Figures 相似文献