A range of fault slip styles on progressively misoriented planes during flexural-slip folding,Cape Fold Belt,South Africa

Flexural slip folds are distinctive of mixed continuous-discontinuous deformation in the upper crust, as folding is accommodated by continuous bending of layers and localized, discontinuous slip along layer interfaces. The mechanism of localized, layer-parallel slip and the stress and fluid pressure conditions at which flexural slip occurs are therefore distinctive of shear localization during distributed deformation. In the Prince Albert Formation mudstone sequence of the Karoo Basin, the foreland basin to the Cape Fold Belt, folds are well developed and associated with incrementally developed bedding-parallel quartz veins with slickenfibers oriented perpendicular to fold hinge lines, locally cross-cutting axial planar cleavage, and showing hanging wall motion toward the fold hinge. Bedding-parallel slickenfiber-coated veins dip at angles from 18° to 83°, implying that late increments of bedding-parallel shear occurred along unfavorably oriented planes. The local presence of tensile veins, in mutually cross-cutting relationship with bedding-parallel, slickenfiber-coated veins, indicate local fluid pressures in excess of the least compressive stress.Slickenfiber vein microstructures include a range of quartz morphologies, dominantly blocky to elongate-blocky, but in places euhedral to subhedral; the veins are commonly laminated, with layers of quartz separated by bedding-parallel slip surfaces characterized by a quartz-phyllosilicate cataclasite. Crack-seal bands imply incremental slickenfiber growth, in increments from tens of micrometers to a few millimeters, in some places, whereas other vein layers lack evidence for incremental growth and likely formed in single slip events. Single slip events, however, also involved quartz growth into open space, and are inferred to have formed by stick-slip faulting. Overall, therefore, flexural slip in this location involved bedding-parallel faulting, along progressively misoriented weak planes, with a range of slip increments.     

南秦岭主要类型热水沉积岩的REE地球化学

南秦岭泥盆纪沉积柱中产有多种类型海底热水沉积岩．它们的ΣＲＥＥ偏低（平均６３．０９×１０－６），ＲＥＥ配分曲线平缓右倾，Ｌａ／Ｙｂ＝２～８，Ｃｅ亏损，总体上与海水相似。产于Ｓｅｄｅｘ含矿层中的热水沉积岩具有正Ｅｕ异常，与现代海底热液及红海热液沉积物可比；而产在Ｓｅｄｅｘ含矿层以下地层中的热水沉积岩Ｅｕ亏损，与ＥＰＲ热液沉积物相似。ＲＥＥ地球化学研究和岩石学研究结果一致，支持热水沉积岩ＲＥＥ来源于海水及部分下伏沉积柱（包括基底），含矿热水沉积岩是盆地热演化到一定阶段具有一定深度和规模的循环对流体系在海底的化学沉积，而Ｓｅｄｅｘ含矿层以下地层中的热水沉积岩则是浅部热水对流循环的海底显示．成岩和变质作用对岩石的ＲＥＥ未造成影响。     

乔治王岛菲尔德斯半岛的地温特征和岩石热物理性质

1985—1986年度和1986—1987年度在菲尔德斯半岛对地面温度进行了测量,共获得129个数据,并对带回的样品进行了岩石热导率测量,共获得210个数据。本文在分析和归纳这些数据的基础上对菲尔德斯半岛的地温特征和岩石热物理性质进行了初步探讨。     

Solubility of Anhydrite, CaSO4, in NaCl-H2O Solutions at High Pressures and Temperatures: Applications to Fluid-Rock Interaction

Anhydrite solubility in H₂O–NaCl solutions was measuredat 6–14 kbar, 600–800°C and NaCl mole fractions(X_NaCl) of 0–0·3 in piston–cylinder apparatus.Solubilities were determined by weight changes of natural anhydritein perforated Pt envelopes confined with fluid in larger Ptcapsules. In initially pure H₂O at 10 kbar and 800°C, CaSO₄concentration is low (0·03 molal), though much largerthan at the same temperature and 1 kbar. Hematite-buffered experimentsshowed slightly lower solubilities than unbuffered runs. CaSO₄solubility increases enormously with NaCl activity: at 800°Cand 10 kbar and X_NaCl of 0·3, CaSO₄ molality is 200 timeshigher than with pure H₂O. Whereas CaSO₄ solubility in pureH₂O decreases with rising T at low T and P, the high-P resultsshow that anhydrite solubility increases with T at constantP at all X_NaCl investigated. The effects of salinity and temperatureare so great at 10 kbar that critical mixing between sulfate-richhydrosaline melts and aqueous salt solutions is probable at900°C at X_NaCl 0·3. Recent experimental evidencethat volatile-laden magmas crystallizing in the deep crust mayevolve concentrated salt solutions could, in light of the presentwork, have important implications regarding such diverse processesas Mount Pinatubo-type S-rich volcanism, high-f O₂ regionalmetamorphism, and emplacement of porphyry Cu–Mo ore bodies,where anhydrite–hematite alteration and fluid inclusionsreveal the action of very oxidized saline solutions rich insulfur. KEY WORDS: anhydrite; sulfur; solubility; metamorphic brines; granulites     

Diffuse CO<Subscript>2</Subscript> degassing at Vesuvio,Italy

At Vesuvio, a significant fraction of the rising hydrothermal–volcanic fluids is subjected to a condensation and separation process producing a CO₂–rich gas phase, mainly expulsed through soil diffuse degassing from well defined areas called diffuse degassing structures (DDS), and a liquid phase that flows towards the outer part of the volcanic cone. A large amount of thermal energy is associated with the steam condensation process and subsequent cooling of the liquid phase. The total amount of volcanic–hydrothermal CO₂ discharged through diffuse degassing has been computed through a sequential Gaussian simulation (sGs) approach based on several hundred accumulation chamber measurements and, at the time of the survey, amounted to 151 t d^–1. The steam associated with the CO₂ output, computed assuming that the original H₂O/CO₂ ratio of hydrothermal fluids is preserved in fumarolic effluents, is 553 t d^–1, and the energy produced by the steam condensation and cooling of the liquid phase is 1.47×10¹² J d^–1 (17 MW). The location of the CO₂ and temperature anomalies show that most of the gas is discharged from the inner part of the crater and suggests that crater morphology and local stratigraphy exert strong control on CO₂ degassing and subsurface steam condensation. The amounts of gas and energy released by Vesuvio are comparable to those released by other volcanic degassing areas of the world and their estimates, through periodic surveys of soil CO₂ flux, can constitute a useful tool to monitor volcanic activity.Editorial responsibility: H. Shinohara     

Using the geologic setting of talc deposits as an indicator of amphibole asbestos content

This study examined commercial talc deposits in the U.S. and their amphibole-asbestos content. The study found that the talc-forming environment directly influenced the amphibole and amphibole-asbestos content of the talc deposit. Large talc districts in the U.S. have mined hydrothermal talcs that replaced dolostone. Hydrothermal talcs, created by siliceous fluids heated by magmas at depth, consistently lack amphiboles as accessory minerals. In contrast, mineable talc deposits that formed by contact or regional metamorphism consistently contain amphiboles, locally as asbestiform varieties. Examples of contact metamorphic deposits occur in Death Valley, California; these talc-tremolite deposits contain accessory amphibole-asbestos. Talc bodies formed by regional metamorphism always contain amphiboles, which display a variety of compositions and habits, including asbestiform. Some industrial mineral deposits are under scrutiny as potential sources of accessory asbestos minerals. Recognizing consistent relations between the talc-forming environment and amphibole-asbestos content may be used in prioritizing remediation or monitoring of abandoned and active talc mines.     

Hydrothermal mixing,carbonate dissolution and sulfide precipitation in Mississippi Valley-type deposits

A large number of Mississippi Valley-Type (MVT) deposits are located within dissolution zones in carbonate host rocks. Some genetic models propose the existence of cavities generated by an earlier event such as a shallow karstification, that were subsequently filled with hydrothermal minerals. Alternative models propose carbonate dissolution caused by the simultaneous precipitation of sulfides. These models fail to explain either the deep geological setting of the cavities, or the observational features which suggest that the dissolution of carbonates and the precipitation of minerals filling the cavities are not strictly coeval. We present a genetic model inspired by the textural characteristics of MVT deposits that accounts for both the dissolution of carbonate and precipitation of sulfides and later carbonates in variable volumes. The model is based on the mixing of two hydrothermal fluids with a different chemistry. Depending on the proportion of the end members, the mixture dissolves and precipitates carbonates even though the two mixing solutions are both independently saturated in carbonates. We perform reactive transport simulations of mixing of a regional groundwater and brine ascending through a fracture, both saturated in calcite, but with different overall chemistries (Ca and carbonate concentrations, pH, etc). As a result of the intrinsic effects of chemical mixing, a carbonate dissolution zone, which is enhanced by acid brines, appears above the fracture, and another zone of calcite precipitation builds up between the cavity and the surrounding rock. Sulfide forms near the fracture and occupies a volume smaller than the cavity. A decline of the fluid flux in the fracture would cause the precipitation of calcite within the previously formed cavities. Therefore, dissolution of carbonate host rock, sulfide precipitation within the forming cavity, and later filling by carbonates may be part of the same overall process of mixing of fluids in the carbonate host rock.Editorial handling: C. Everett     

Geology and geochemistry of the Changba SEDEX Pb-Zn deposit,Qinling orogenic belt,China

The Changba Pb-Zn SEDEX deposit occurs in the Middle Devonian sequence of the Anjiaca Formation of the Western Qinling Hercynian Orogen in the Gansu Province, China. The Changba-II orebody is hosted in biotite quartz schist and is the largest of 143 stratiform orebodies that are hosted either in biotite quartz schist or marble. The Changba-II comprises two types of mineralization: a bedded facies and an underlying breccia lens. The bedded section exhibits three sulfide sub-facies zoned from bottom to top: 1) banded sphalerite intercalated with quartz albitite; 2) interbedded massive pyrite and sphalerite ore; and 3) banded sphalerite ore intercalated with banded baritite. Major metallic minerals are sphalerite, pyrite, galena, with minor arsenopyrite, pyrrhotite, boulangerite, and rare chalcopyrite. The bedded sulfides are underlain by a lens of brecciated and albitized biotite-quartz schists cemented by sulfides and tourmaline.Massive and bedded sulfide ³⁴S values range from 8.1 to 29.3, whereas barite ³⁴S values range from 20.8 to 31.5. Disseminated pyrite in footwall schists has ³⁴S values ranging from 8.1 to 10.6, and increase to values ranging from 11.1 to 14.7 in the hangingwall. The lower ³⁴S values for massive and bedded sulfides are interpreted to be derived from progressive bacterial sulfate reduction (BSR) of Devonian seawater in a sulfate-restricted sub-basin. The higher ³⁴S values for massive and bedded sulfides could be a product of quantitative BSR but this is incompatible with barite being more abundant above the bedded sulfides. Instead, it is more likely that thermochemical sulfate reduction of seawater sulfate or of evaporite was the source of heavy hydrothermal sulfur. Heavy hydrothermal sulfur was injected into a sulfate-restricted sub-basin where it mixed with low ³⁴S BSR sulfide to form the massive and bedded sulfides. The REE patterns of sulfide layers and associated quartz albitite and baritite are similar to those of the host biotite quartz schists, suggesting that the hydrothermal fluids leached REE from the underlying rocks. Pb isotope ratios in galena form an array between the Upper Crust and the Mantle reservoir curves, which indicates that the lead is derived from upper crustal rocks comprising mafic igneous units. The Sr⁸⁷/Sr⁸⁶ ratio of 0.7101 for carbonate within the sulfide layers also suggests that Sr is derived from the mixing of Sr leached from upper crustal rocks with Middle Devonian seawater Sr. A Rb-Sr isochron age of 389.4 ± 6.4 Ma for sulfide layers and the interbedded hydrothermal sediments is consistent with the age of host Mid-Devonian strata. Ar³⁹/Ar⁴⁰ plateau age at 352.8 ± 3.5 Ma and Ar³⁹-Ar⁴⁰ isochron age of 346.6 ± 6.4 Ma for albite in the quartz albitite intercalated with sulfide layers indicate either albite formation after the sulfides or thermal resetting of the Rb-Sr system at about 350 Ma, the age of collision between the North China and Yangtze cratons.Editorial handling: E. Frimmel     

Changeable hydrothermal media as potential cradle of life on a planet

According to the elaborated systemic concept, a prebiotic microsystem has a chance to be transformed into primary living unit (probiont) only under nonequilibrium oscillating conditions. This transition proceeds through three successive kinds of transformations. First, a prebiotic microsystem must acquire the specific critical properties being at the unstable state of the bifurcate transition. Then it should be relatively stabilized due to balanced oscillations between the initial and the forward states (there appears the paradoxical state of ‘stabilized instability’). The decisive transformation to the living state is connected with the inversion of the ratio of ‘free energy to entropy contribution’ when the free energy input in the microsystem becomes higher than the entropy input. Changeable nonequilibrium conditions are most typical to hydrothermal systems in comparison with other aqueous media of the Earth. In this context the hydrothermal medium seems very suitable to be considered as a potential cradle of life on a planet. To characterize a scale of the thermodynamic and physico-chemical fluctuations some hydrothermal systems in Kamchatka peninsula were explored. The period of the pressure microoscillations in Mutnovsky and Pauzhetsky hydrothermal systems range from 10 to 30 min, and the amplitude is 0.2-0.7 bar. From time to time the amplitude of the fluctuations significantly rises due to spontaneous increase of activity of the nearest volcanoes. Similar results were obtained during the exploration of thermodynamic and chemical fluctuations in Mura hydrothermal field in Slovenia: the period of the water pressure oscillations is 60-70 min, and the average amplitude about 0.5 bar. Temperature and some chemical parameters oscillate in this field with the same period. These data can be used to conduct advanced laboratory experiments on prebiotic organic synthesis under nonequilibrium oscillating conditions. Some universal aspects of this concept may allow us to better understand the origin-of-life process in the Universe.     

Geochemical constraints on the modes of carbonate precipitation in peridotites from the Logatchev Hydrothermal Vent Field and Gakkel Ridge

The ultramafic-hosted Logatchev Hydrothermal Field (LHF) at 15°N on the Mid-Atlantic Ridge and the Arctic Gakkel Ridge (GR) feature carbonate precipitates (aragonite, calcite, and dolomite) in voids and fractures within different types of host rocks. We present chemical and Sr isotopic compositions of these different carbonates to examine the conditions that led to their formation. Our data reveal that different processes have led to the precipitation of carbonates in the various settings. Seawater-like ⁸⁷Sr/⁸⁶Sr ratios for aragonite in serpentinites (0.70909 to 0.70917) from the LHF are similar to those of aragonite from the GR (0.70912 to 0.70917) and indicate aragonite precipitation from seawater at ambient conditions at both sites. Aragonite veins in sulfide breccias from LHF also have seawater-like Sr isotope compositions (0.70909 to 0.70915), however, their rare earth element (REE) patterns show a clear positive europium (Eu) anomaly indicative of a small (< 1%) hydrothermal contribution. In contrast to aragonite, dolomite from the LHF has precipitated at much higher temperatures (~ 100 °C), and yet its ⁸⁷Sr/⁸⁶Sr ratios (0.70896 to 0.70907) are only slightly lower than those of aragonite. Even higher temperatures are calculated for the precipitation of deformed calcite veins in serpentine–talc fault schists form north of the LHF. These calcites show unradiogenic ⁸⁷Sr/⁸⁶Sr ratios (0.70460 to 0.70499) indicative of precipitation from evolved hydrothermal fluids. A simple mixing model based on Sr mass balance and enthalpy conservation indicates strongly variable conditions of fluid mixing and heat transfers involved in carbonate formation. Dolomite precipitated from a mixture of 97% seawater and 3% hydrothermal fluid that should have had a temperature of approximately 14 °C assuming that no heat was transferred. The much higher apparent precipitation temperatures based on oxygen isotopes (~ 100 °C) may be indicative of conductive heating, probably of seawater prior to mixing. The hydrothermal calcite in the fault schist has precipitated from a mixture of 67% hydrothermal fluid and 33% seawater, which should have had an isenthalpic mixing temperature of ~ 250 °C. The significantly lower temperatures calculated from oxygen isotopes are likely due to conductive cooling of hydrothermal fluid discharging along faults. Rare earth element patterns corroborate the results of the mixing model, since the hydrothermal calcite, which formed from waters with the greatest hydrothermal contribution, has REE patterns that closely resemble those of vent fluids from the LHF. Our results demonstrate, for the first time, that (1) precipitation from pure seawater, (2) conductive heating of seawater, and (3) conductive cooling of hydrothermal fluids in the sub-seafloor all can lead to carbonate precipitation within a single ultramafic-hosted hydrothermal system.