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1.
Jörg Erzinger 《International Journal of Earth Sciences》1989,78(3):731-740
The alteration of the upper oceanic crust through sea water-basement rock interaction produces different and distinct alteration zones with increasing depth. The zonation generally shows a consistent worldwide pattern.The uppermost basement is influenced by oxidative sea water-basalt alteration at low temperatures and high water/rock ratios. With increasing crustal depth or even in a single pillow the temperatures rise, the water/rock ratios become lower, the redox and pH values normally decrease, and the oxidative zone is followed by a non-oxidative one. Below these zones the basement has suffered high-temperature alteration under reducing and acidic conditions.This results in chemical modifications of the rocks by the addition or leaching of certain elements, and has also consequences for the composition of sea water.From our own data and data presently available in the literature I summarize the mineralogical and geochemical characteristica of sea water alteration processes affecting the oceanic crust.
Zusammenfassung Die chemische Veränderung der oberen ozeanischen Kruste durch Gestein/Meerwasser-Interaktionen produziert verschiedene und unterscheidbare Alterationszonen die von der Krustentiefe abhängig sind. Diese Zonierung zeigt weltweit vergleichbare Muster.Das oberste Basement wird von einer niedrig temperierten oxidativen Meerwasseralteration beeinflußt. Mit zunehmender Krustentiefe steigen die Reaktionstemperaturen an, die Redox- und pH-Werte werden kleiner, d.h. nichtoxidative Alterationsvorgänge dominieren. Unterhalb dieser Zonen wird die ozeanische Kruste überwiegend von reduzierenden und sauren Hydrothermallösungen alteriert.Im Verlauf der Seewasser/Basalt-Reaktionen werden die Gesteine mineralogisch und chemisch verändert, indem verschiedene Elemente aus den Basalten herausgelöst und wiederum andere aufgenommen werden. Diese Vorgänge haben auch für die Zusammensetzung des Meerwassers drastische Konsequenzen.Mit Hilfe publizierter aber vor allem mit eigenen Daten werden die mineralogischen und geochemischen Charakteristika der unterschiedlichen Alterationsprozesse zusammengefaßt dargestellt.
Résumé L'altération de la partie supérieure de la croûte océanique sous l'action de l'eau de mer engendre plusieurs zones distinctes qui se succèdent de haut en bas. Ce zonage présente d'ordinaire une extension mondiale.La partie supérieure de la croûte est affectée d'une altération oxydante de basse température du basalte. Vers le bas, parfois même au sein d'un même pillow, la température s'élève, la quantité d'eau décroît, le potentiel redox et le pH diminuent, de sorte que la zone d'oxydation est suivie d'une zone non oxydante. En-dessous de ces deux zones, les roches ont subi une altération de haute température dans des conditions acides et réductrices.Il en résulte des changements de la composition chimique des roches par apport ou par lessivage de certains élements, ainsi qu'une modification de la composition de l'eau de mer.A partir des données de la littérature et surtout de mes propres observations, je présente une synthèse des caractères minéralogiques et géochimiques des divers processus de l'altération sous-marine.
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2.
The platinum-group elements (PGE) and gold have been determined in twenty international rock reference materials by inductively coupled plasma-mass spectrometry (ICP-MS) after pre-concentration by a nickel sulfide fire assay. It was possible to achieve determination limits for a 50 g sample that ranged from 1 pg g-1 (Rh) to 23 pg g-1 (Au). Compared to published certified and recommended values for rock reference materials, the trueness of the method was found to be good. However, in some cases we observed large deviations for all elements in the sub 10 ng g-1 range within individual reference sample splits. Our results show that the PGE and Au are inhomogeneously distributed in the reference materials analysed here, where they are present in low concentrations, using 50 g test portions. 相似文献
3.
Erzinger Jörg Hinz Karl Sibuet Jean-Claude Talwani Manik 《Marine Geophysical Researches》1998,20(4):251-252
Marine Geophysical Research - 相似文献
4.
The geochemical effects of brine and supercritical CO2 (SCCO2) on reservoir rocks from deep (1500–2000 m) saline aquifers were examined via experimental simulation at in situ conditions. Dry sandstone samples were mounted in a triaxial cell and autoclave system, evacuated, and saturated with 1 M NaCl solution. The brine-rock system was allowed to react at 30 MPa confining pressure, 15 MPa pore fluid pressure, and 60 °C while SCCO2 was injected at a pressure gradient of 1–2 MPa. The experiment was conducted for a period of 1496 h, during which fluids were periodically sampled and analyzed. The pH measured in partially degassed fluid samples at 25 °C decreased from a starting value of 7.0–4.3 (9 days) and finally 5.1 after saturation with SCCO2. 相似文献
5.
Boron recycling in the continental crust of the central Andes from the Palaeozoic to Mesozoic, NW Argentina 总被引：4，自引：2，他引：2
Simone Kasemann Jörg Erzinger Gerhard Franz 《Contributions to Mineralogy and Petrology》2000,140(3):328-343
Whole-rock chemical composition and 11B/10B isotope ratios in tourmaline was investigated to study the geochemical recycling of boron during the evolution of the Andean
basement from the Palaeozoic to Mesozoic. In the basement (Cambrian to Ordovician high-grade paragneisses, migmatites and
orthogneisses, the Eocambrian Puncoviscana Formation, and Paleozoic-Mesozoic granitoid igneous rocks) whole-rock B contents
are generally below 100 ppm, but B contents of ˜1 wt% are found in cogenetic aplite and pegmatite dikes and in tourmaline–quartz
rocks. In the metasedimentary rocks, no systematic variation in B content because of metamorphic grade and no correlation
of B with other incompatible elements are apparent. Tourmalines from the high-grade metamorphic basement yield δ11B values ranging from −11.2 to −6.8‰ and isotope fractionation during migmatisation was small. Metamorphic tourmalines from
the Puncoviscana Formation have δ11B values between −6.3 and −5.8‰. The calculated (corrected for fractionation) δ11B values of −6 to −2‰ for the sedimentary protolith of the metamorphic basement indicate a continental B source with subordinate
marine input. Tourmalines from Palaeozoic and Mesozoic granitoids display an identical range of δ11B values from −12 to −5.3‰ and indicate a similarly homogeneous B source throughout time. Tourmalines from pegmatites and
tourmaline–quartz rocks record the average δ11B values of the parental granitic magma. We assume that B in the Palaeozoic and Mesozoic granitoids is derived from the local
metamorphic basement supporting the hypothesis that recycling of the lower Palaeozoic crust is the dominant process in granitic
magma formation from Palaeozoic to Mesozoic.
Received: 15 December 1999 / Accepted: 11 July 2000 相似文献
6.
Johanna Lippmann-Pipke Jörg Erzinger Martin Zimmer Christian Kujawa Margaret Boettcher Esta Van Heerden Armand Bester Hannes Moller Nicole A. Stroncik Zeev Reches 《Applied Geochemistry》2011,26(12):2134-2146
An on-site gas monitoring study has been conducted in the framework of an earthquake laboratory (The International NELSAM–DAFGAS projects) at the TauTona gold mine, South Africa. Five boreholes up to 60 m long were drilled at 3.54 km depth into the highly fractured Pretorius Fault Zone and instruments for chemical and seismic monitoring installed therein. Over the span of 4 years sensitive gas monitoring devices were continuously improved to enable the direct observation of geogas concentration variations in the DAFGAS borehole. The major gas concentrations are constant and air-like with about 78% N2, 21% O2, 1% Ar. The geogas components CO2, CH4, He and H2 show the most interesting trends and variations on the minute-by-minute basis and significantly correlate with seismic data, while the 222Rn activity remains constant. Time series and cross correlation analysis allow the identification of different gas components (geogas and tunnel air) and the identification of two processes influencing the borehole gas composition: (1) pumping-induced tunnel air breakthrough through networks of initially water-saturated fault fractures; and (2) seismicity induced permeability enhancement of fault fractures to above ∼5 × 10-10 m2. The current set-up of the gas monitoring system is sensitive enough to quantify the resulting geogas transport during periods of intense blasting activities (including recorded blasts with seismic moment ?1 × 109 Nm, located within 1000 m of the cubby) and, it is suggested, also during induced earthquakes, a final goal of the project. 相似文献
7.
Simone A. Kasemann Anette Meixner Jrg Erzinger Jos G. Viramonte Ricardo N. Alonso Gerhard Franz 《Journal of South American Earth Sciences》2004,16(8):2562
We have measured the boron concentration and isotope composition of regionally expansive borate deposits and geothermal fluids from the Cenozoic geothermal system of the Argentine Puna Plateau in the central Andes. The borate minerals borax, colemanite, hydroboracite, inderite, inyoite, kernite, teruggite, tincalconite, and ulexite span a wide range of δ11B values from −29.5 to −0.3‰, whereas fluids cover a range from −18.3 to 0.7‰. The data from recent coexisting borate minerals and fluids allow for the calculation of the isotope composition of the ancient mineralizing fluids and thus for the constraint of the isotope composition of the source rocks sampled by the fluids. The boron isotope composition of ancient mineralizing fluids appears uniform throughout the section of precipitates at a given locality and similar to values obtained from recent thermal fluids. These findings support models that suggest uniform and stable climatic, magmatic, and tectonic conditions during the past 8 million years in this part of the central Andes. Boron in fluids is derived from different sources, depending on the drainage system and local country rocks. One significant boron source is the Paleozoic basement, which has a whole-rock isotopic composition of δ11B=−8.9±2.2‰ (1 SD); another important boron contribution comes from Neogene-Pleistocene ignimbrites (δ11B=−3.8±2.8‰, 1 SD). Cenozoic andesites and Mesozoic limestones (δ11B≤+8‰) provide a potential third boron source. 相似文献
8.
Süer Selin Wiersberg Thomas Güleç Nilgün Erzinger Jörg Parlaktuna Mahmut 《Natural Hazards》2020,104(2):1655-1678
Natural Hazards - This study presents the results of a real-time gas monitoring experiment conducted, via the use of a quadrupole mass spectrometer, in a mofette field within the Tekke Hamam... 相似文献
9.
Steven Goderis Elin Kalleson Roald Tagle Henning Dypvik Ralf-Thomas Schmitt Jörg Erzinger Philippe Claeys 《Chemical Geology》2009,258(3-4):145-156
The goal of this study is to identify the type of projectile responsible for the formation of the late Precambrian Gardnos impact structure in Norway. Fifteen impactite samples, predominantly impact breccias and suevites from the central and northeastern part of the structure, were analyzed for platinum group elements (PGE) and Au using nickel-sulfide fire assay combined with inductively coupled plasma mass spectrometry (ICP-MS). Major and trace elements were measured in the same samples using X-ray fluorescence (XRF). In addition, the concentrations of siderophile elements Ni, Cr, and Co were determined by ICP-MS after acid digestion. The samples collected at the contact between suevite and the sedimentary infill yielded the highest PGE concentrations (Ir = 1.926 ng/g, Ru = 3.494 ng/g, Pt = 4.716 ng/g, Rh = 0.766 ng/g, Pd = 2.842 ng/g for GC6). The CI-normalized PGE patterns are characterized by Ru and Rh enrichments suggesting a non-chondritic impactor. Concentration plots of the different PGE display an excellent correlation (R > 0.99), indicative of a single source for the PGE enrichment. The Ni/Cr ratio of the Gardnos impactor (2.56 ± 0.20) agrees with that of chondrites (2 to 7), whereas Ir is depleted relative to Ni in this projectile (Ni/Ir ratio of 92 000 ± 8000 compared to an average Ni/Ir ratio of 23 150 ± 4250 for chondrites). There is no clear indication of selective post-depositional remobilization of the characteristic highly siderophile elements. The Ni/Ir and Cr/Ir data combined with the non-chondritic PGE ratios probably indicate a differentiated projectile. Based on (1) the similarity of the inter-element ratios of the impactor with the iron phase of non-magmatic iron meteorites and (2) the presence of characteristics of both chondrites and iron meteorites (Ni/Cr and Ni/Ir ratios), an IA or IIIC non-magmatic iron meteorite is a very plausible impactor. 相似文献
10.
Hammerschmidt Sebastian B Wiersberg Thomas Heuer Verena B Wendt Jenny Erzinger Jörg Kopf Achim 《Geochemical transactions》2014,15(1):1-9