Coeval potassic and sodic calc-alkaline series in the post-collisional Hercynian Tanncherfi intrusive complex, northeastern Morocco: geochemical, isotopic and geochronological evidence

The post-collisional late Hercynian Tanncherfi intrusive complex (TIC) is part of a widespread intrusive episode in the Moroccan Meseta. The complex contains a wide range of rock types, from monzogabbros to monzogranites. Two distinct magmatic series are recognized: (1) a potassic (shoshonitic) series consisting of monzogabbros, quartz monzonites and monzogranites; and (2) a sodic (granodioritic) series represented by quartz monzodiorites and granodiorites. All the Tanncherfi plutonic rocks display similar spider-diagram profiles, with LILE and LREE enrichment and Nb, Ta, Ti depletion, which are typical of subduction-related magmas. Combined major, trace element compositions and Sr, Nd isotopic results indicate that the two series have been derived from a LILE- and LREE-enriched continental lithospheric mantle source, under different partial melting and/or depth conditions. Intrusion of the Tanncherfi rocks was not temporally related to subduction and the enrichment of their source is likely to be linked to preceding subduction events. The two series evolved by fractional crystallization, of clinopyroxene, plagioclase, hornblende, biotite, K-feldspar and accessories (Fe–Ti oxide minerals, titanite, apatite and zircon) for the potassic series while the sodic series combined fractional crystallization with assimilation of felsic magmas with lower Sr isotopic ratio than the more mafic term of the series, the quartz monzodiorite. The intrusion of the potassic magmas (344±6 Ma) marks a major change in the tectonic regime of eastern Meseta. These magmas intruded during post-thickening uplift and extension, both probably favored by convective thinning of the lithosphere. This model provides a reasonable mechanism for the genesis of other Hercynian intrusive complexes in Morocco.     

Groundwater circulation in the allochthonous limestone units between Lake Girdev and Kazanpınarı Spring, Antalya, southwestern Turkey

 The aim of the study is to investigate the interaction between waters of Lake Girdev and groundwater in the allochthonous limestone units exposed in the area between Lake Girdev and Kazanpınarı Spring, southwestern Turkey. The features analyzed include the flow direction and apparent groundwater velocity, their relationship with Lake Girdev, and the effect of lithological and structural features on the groundwater circulation. The results of a fluorescein tracer test indicate that groundwater flows east-northeast and the apparent flow velocity ranges from 26.2 to 35.6 m h^–1 between the injection site and various observation points. Tritium data suggest that the water of Lake Girdev and groundwater are probably similar in age, and oxygen-18 isotope data indicate that water derived from Lake Girdev is the main source of recharge to the aquifer. The aquifer is fed not only by Lake Girdev but also by rainfall percolating through allochthonous limestones; together, these provide the discharge of springs in Elmalı Polje. The permeability of the allochthonous limestone aquifer has been enhanced as a result of jointing and faulting. Received, June 1997 / Revised, June 1998, March 1999 / Accepted, July 1999     

Hydrochemical and isotopic properties of the Mahmutlu and Bağdatoğlu mineralized thermal springs, Kırşehir, Turkey

The present study identifies the hydrochemical and isotopic properties of the Mahmutlu and Ba?dato?lu mineralized thermal springs in K?r?ehir province, a geothermal field in central Anatolia, Turkey. Based on these properties, a hydrogeological regime is proposed in order to explain the Mahmutlu–Ba?dato?lu geothermal system. The relation between the concentrations of the environmental stable isotopes deuterium and oxygen-18 in the water is similar to the relationship in global meteoric water, indicating that the water is of meteoric origin. Evaluation of the geochemical characteristics of the water reveals that these two thermal springs belong to the same hydrogeological system. The hydrogeological system comprises a fractured limestone member of the Çevirme Formation and the Kervansaray Formation as reservoir rocks, and the Delice?rmak Formation as an overlying aquitard. The waters of the Mahmutlu and Ba?dato?lu springs are mainly of the Na-Cl-SO4 type that originate from the Pohrenk evaporite. The thermal waters are undersaturated with respect to calcite, dolomite, halite, and gypsum. The δ 18O and δ 2H contents indicate a δ 18O shift in the Mahmutlu and Ba?dato?lu waters. The temperature range of the two reservoirs is estimated to be 98–158?°C, on the basis of Na+K+Ca and SiO2 geothermometers.     

从花岗岩的Sm—Nd同位素探讨华南中下地壳的组成,性质和演化

现有２４０个花岗岩体的Ｎｄ同位素资料表明,华南内陆花岗岩可能主要由地壳部分熔融成成。从壳源花岗岩提取源岩成分信息的方法是把这种花岗岩的同位素成分同出露的元古代弱变质地壳的相应资料作比较。野外关系说明,华南内陆花岗岩侵入毗邻的围岩,因此其形成深度应该出现在出露的深度大。。因为这些花岗岩的定位深度一般在5～15km之间,这些壳源花岗岩可能代表一种中地壳探度的熔融．它们的同位索成分应能提供在这一探度上地壳成分的信息。根据华南壳源花岗岩同出露的元古代弱变质地壳岩石的Sm—Nd同位素对比,华南内陆大部分地区在中地壳探度上存在中性至长英质成分的地壳,并且从早古生代到中生代不曾发生过明显变化。但是花岗岩浆的分异作用所导致的Sm、Nd分馏可能是亲石元素矿化的一个重要控制因素。     

Boron isotopic composition of subduction-zone metamorphic rocks

Many arc lavas contain material derived from subducted oceanic crust and sediments, but it remains unresolved whether this distinctive geochemical signature is transferred from the subducting slab by aqueous fluids, silicate melts, or both. Boron isotopic measurements have the potential to distinguish between slab transfer mechanisms because ¹¹B fractionates preferentially into aqueous fluids whereas little fractionation may occur during partial melting. Previous studies have shown that δ¹¹B values of island arc lavas (−6 to +7) overlap the range of δ¹¹B values for altered oceanic crust (−5 to +25) and pelagic sediments and turbidites (−7 to +11). Secondary ion mass spectrometry (SIMS) analyses of minerals in subduction-zone metamorphic rocks yield δ¹¹B=−11 to −3 suggesting that slab dehydration reactions significantly lower the δ¹¹B values of subducted oceanic crust and sediments. In order to explain the higher δ¹¹B values reported for arc lavas as compared to subduction-zone metamorphic rocks, the B-bearing component derived from the metamorphosed slab must be enriched in ¹¹B relative to the slab, favoring an aqueous fluid as the slab transfer mechanism.     

Pathways and distances of fluid flow during low-grade metamorphism: evidence from pyrite deposits of the Cameros Basin, Spain

New geochemical and sulphur isotopic data are presented for a number of pyrite deposits from the Late Jurassic–Early Cretaceous Cameros Basin, Spain. The deposits were formed at, or close to, the peak of metamorphism and are always related to sandstone units in the mainly metapelite sequence. Iron remained immobile and conservative, pyrite iron being derived by sulphidation of chlorite in the host metapelites. Reduced sulphur, however, was supplied from two external sources: thermochemical reduction of sulphate and release of S during metamorphism of sedimentary sulphides. These sources provided isotopically heavy and light S, respectively, with variation in pyrite isotopic composition between different deposits resulting from differences in their relative importance at each site. During metamorphism, the sandstone units acted as aquifers, carrying the sulphidic pore waters to locations where permeability provided by syn-depositional fractures on a scale of 0.5–5  m allowed its interaction with the metapelites. Transport distances for sulphide during metamorphism were of the order of hundreds of metres.     

赣中变质岩带的Sm—Nd,Rb—Sr同位素年代研究

赣中变质岩带主要由斜长(云母)变粒岩、十字石榴云母片岩、云母石英片岩夹斜长角闪岩组成。斜长角闪岩Sm-Nd全岩等时线年龄为1113±19Ma,相当于该变质岩带的原岩形成年龄。ε_(Nd)(t)值为2.4±0.1,说明岩浆起源于亏损程度较低的地幔源区:726.6±1.1Ma、403.1±6.4Ma的Rb-Sr等时线年龄表明赣中地区在新元古代末期、加里东期经历了一次强烈的构造变质热作用,其地质、地球化学特征及时代可与浙闽地区陈蔡群、建瓯群进行对比。因此赣中变质岩带并非长期公认的华南加里东褶皱带,应是华夏地块的一部分,这一事实对华南大地构造单元的划分及构造演化具有重要意义。     

Hydrogen and oxygen isotope studies of metamorphic fluid-rock interactions in the Dabie Mountains

Hydrogen and oxygen isotope studies were carried out on mineral separates from high to ultrahigh pressure metamorphic rocks at Huangzhen and Shuanghe in the eastern Dabie Mountains, East China. The δ¹⁸O values of eclogites cover a wide range of −5‰ to+9‰, but the δD values of micas fall within a narrow range of −85% to −70‰. Both equilibrium and disequilibrium oxygen isotope fractionations were observed between quartz and the other minerals, with reversed fractionations between omphacite and garnet in some eclogite samples. The δ¹⁸ O values of −5‰ to −1‰ for some of the eclogites represent the oxygen isotope compositions of their protoliths which underwent meteoric water-rock interaction prior to plate subduction. The preservation of oxygen isotope heterogeneity in the eclogites implies a channelized flow of fluids during progressive metamorphism caused by rapid subduction. Retrograde metamorphism has caused oxygen and hydrogen isotope disequilibria between some of the minerals, but the fluid for retrograde reactions was internally buffered in the stable isotope compositions. Project supported by the Chinese Ministry of Science and Technology (Grant No. 95-Pre-39), the National Natural Science Foundation of China (Grant Nos. 49794042, 49473173 and 49453003) and the Chinese Academy of Sciences (Grant No. KZ951-A1-401-5)     

Organic carbon isotopes of the Sinian and Early Cambrian black shales on Yangtze Platform, China

Organic matter of the Sinian and early Cambrian black shales on the Yangtze Platform belongs to the light carhon group of isotopes with the δ¹³C values from - 27% to - 35 %, which are lower than those of the contempomneously deposited carbonates and phosphorites. A carbon isotope-stratified paleooceanographic model caused by upwelling is proposed, which can be used not only to interpret the characteristies of organic carbon isotopic compositions of the black shales, but also to interpret the paleogeographic difference in the organic carbon isotope compositions of various types of sedimentary rocks. Project supported by the National Natural Science Foundation of China (Grant No. 49472114) and the Open Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences.     

Depositional environment of a Kimmeridgian carbonate 'black band' (Akkuyu Formation, south-western Turkey)

The Upper Jurassic Akkuyu Formation of south-western Turkey consists of pale-coloured carbonate facies, but includes a peculiar ‘black band’ at its base. In order to characterize the depositional environment of this level, a sedimentological, organic and inorganic geochemical study was performed on 30 samples. Three units are distinguished. Unit 1 consists of black marlstones, very rich in organic carbon (22–30%) with HI (hydrogen index) values around 600. The organic matter is an amorphous homogeneous material even at nanoscopic scale. This unit is also characterized by a very high concentration of V ( >1000 p.p.m.) and a δ¹³C_org value around ?26·5‰. Unit 2 shows thin-bedded black limestones with chert layers. Its organic content varies from 2% to 6%. As in unit 1, the HI values are uniformly high (600), and gas chromatography shows a high quantity of hopanes. The V concentration is also high (≈400 p.p.m.). The unit has a high Sr/Ca ratio, an organic carbon isotopic ratio close to ?28·7‰ and diffuse, nanoscopically amorphous organic material that is closely associated with pyrite. Unit 3 corresponds to the white limestones overlying the ‘black band’. This calcitic facies is almost devoid of organic carbon (<0·1%). The δ¹³C_org values are similar to those of unit 1 (?25·5‰ to ?26‰). Deposition occurred in a basinal environment surrounded by a carbonate platform. Primary productivity was high but not exceptional; terrestrial organic inputs were scarce. Bottom waters were probably euxinic during the deposition of unit 1. The presence of both hopane-rich and sulphur-rich nanoscopically amorphous organic matter may be the result of strong sulphate-reducing bacterial activity. Coupled with low amounts of iron, this led to intense vulcanization of the organic matter and thus good preservation. With the onset of unit 2 deposition, environmental conditions became less extreme, perhaps because of cooler water temperatures. Finally, the depositional conditions became oxic, leading to the accumulation of pale-coloured organic-poor limestones of unit 3.