Preliminary investigations of 18O/16O and D/H compositions in rhyo-ignimbrites in the In Hihaou (In Zize) Magmatic Center,central Ahaggar,Algeria

The 620 M.y.-old in Hihaou (In Zize) magmatic complex located at the north-western boundary of the Archaean In Ouzzal block (western Ahaggar), is composed of massive alkaline rhyo-ignimbrites and rhyolitic domes, which are intruded by a granophyric and granitic body. The whole is preserved in a cauldron structure. Extrusive rocks are strongly ¹⁸O-depleted, with -values as low as –1.5/SMOW, while granophyres are less depleted (minimum -¹⁸O value=+2.0/SMOW. The granite has values around + 6/SMOW. D/H compositions are rather low, with D–90 to –110/SMOW. Isotopic zoning of quartz phenocrysts, ¹⁸O/¹⁶O fractionation among coexisting phases, and heterogeneity of the whole-rock -¹⁸O values, suggest that the volcanic rocks have interacted with meteoric water after the eruption. Several mechanisms of isotopic alteration are discussed. The hydrothermal alteration does not seem to have been controlled by the granitic intrusion, but rather seems to have followed the deposition of thick pyroclastic deposits on permeable arkosic sandstones and fluvio-glacial conglomerates. Pervasive circulation of water through the cooling volcanic deposits could have produced the observed ¹⁸O depletion.     

Die isotopische Verteilung von Kohlenstoff und Schwefel in Marmor und anderen Metamorphiten

Zusammenfassung Die C¹²/C¹³-Verhältnisse des Karbonatanteils metamorpher Gesteine liegen mit ihren C¹³-Werten zwischen –8,2 und –22,9 recht niedrig. Die Graphitanteile haben ein C-Isotopenverhältnis –15,7. Prä- bis postkambrischer Marmor aus verschiedenen europäischen Vorkommen ist auf Grund der Isotopenrelationen des Karbonatkohlenstoffs vermutlich marin entstanden. Seine Graphite lassen sich in 2 Gruppen einteilen: Gruppe I mit –19,4 bis –28%.; Gruppe II mit –5,2 bis –16,8. Die S³²/S³⁴-Verhältnisse von sulfidischem Eisenerz aus eklogitischen Gesteinen der Münchberger Gneismasse haben einen relativ kleinen Schwankungsbereich, von 12,0.

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The C¹²/C¹³-ratio of carbonate-carbon in metamorphic rocks is relatively low: C¹³: –8,2 to –22,9; graphitic carbon shows its normal isotopic composition: –15,7. Pre- and postcambrian marbles can be presumed of marine origin on the ground of the isotopic composition of carbonate-carbon whereas their graphites can be divided in two groups: Group I has a C¹²/C¹³-ratio supposed to be typical of organic origin; Group II is surprisingly high in C¹³. The S³²/S³⁴-ratios of ironsulfides from eclogitic rocks (Münchberger Gneismasse) show a relatively narrow spread of 12,0 per mil.

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Résumé Le rapport C¹²/C¹³ du carbone des carbonates dans les roches métamorphiques est relativement petit (C¹³ =–8,2 à –22,9). Le carbone graphitique a sa composition isotopique normale, – 15,7. Les marbres pré- à postcambriens sont probablement marins selon la composition isotopique des carbonates. Leurs graphites forment deux groupes: le premier groupe a des rapports C¹²/C¹³ typiques d'une origine organique, le deuxième groupe contient plus de C¹³ que la normale. Les relations S³²/S³⁴ des sulfures de fer des roches éclogitiques (Münchberger Gneismasse) ne montrent pas de grandes variations isotopiques (12,0).

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¹²/¹³ , . . ¹³ 8,2 22,9 . 15,7 . , , , . : 19,4 28, — 5,2 16,8. S³²/S³⁴ , , 12,0.

     

Sulfur isotopes and origin of some sulfide deposits,New England,Australia

The S-isotopic compositions of sulfide deposits from Steinmann, granitoid and felsic volcanic associations have been examined. Ores of Steinmann association have ³⁴S values close to zero per mil (³⁴S=+0.3±3.1) it appears they are of mantle origin. Isotopically, ores of granitoid association regularly show a variable enrichment in ³²S relative to meteoritic (³⁴S=–2.7±3.3). The composition is in accord with an upper mantle/lower crustal source. Two stratiform accumulations of felsic volcanic association show a narrow spread of ³⁴S values (+0.2 to 2.4); a mantle origin for the sulfur in these deposits is favored. In contrast, vein, stockwork and cement ores are moderately enriched in ³²S relative to meteoritic (³⁴S=–4.0±6.4). These ores are polygenetic; sulfur and metals appear to have been leached from local country rocks where volcanogenic and biogenic sulfur predominate.     

Characteristics and chronology of fracture — fluid infiltration in the Archean,Eye Dashwa Lakes pluton,Superior Province: evidence from H,C, O-isotopes and fluid inclusions

The Archean Eye Dashwa Lakes pluton (2672±24 Ma) has domains of mineralogically fresh isotropic granite, domains that have undergone bulk hydrothermal alteration, and at least eleven sets of sequential fracture arrays, each with distinctive mineral assemblages. Fresh granite is characterized by whole rock ¹⁸O=8.1 to 8.6 and primary magmatic quartz-feldspar (+1.3), quartz-biotite (5.2 to 5.4) and quartz-magnetite (+9.8) fractionations. Magmatic fluids had a calculated isotopic composition of ¹⁸O=7.9±0.5, and D=–80±5. These isotropic volumes of the granite have not experienced significant incursion of external thermal waters. Pegmatites, quartz-molybdenite veins, and phlogopite-muscovite coated fractures are sporadically distributed in the granite, and were precipitated from high-temperature magmatic fluids where ¹⁸O=8.0 to 10.3 and D=–80±5.The most abundant variety of fracture filling assemblage is epidote-quartz-chlorite±muscovite: fractures are bounded by domains of mineralogically similar bulk hydrothermal alteration of the granite. These minerals formed at 160 to 280° C, in the presence of NaCl, and NaCl-MgCl₂ brines (up to 25 wt% NaCl equivalent) of probable evolved marine water origin ( ¹⁸O=+0.4 to +3.8, D=–10 to –35) undergoing transient boiling. Upper plateau ⁴⁰Ar/³⁹Ar ages for the muscovite are 2650±15 Ma. Sequentially in the chronology of fracture-infiltration events, calcite-fluorite veins were deposited from boiling fluids at 340 to 390° C, isotopically characterized by ¹⁸O=4.7 and ¹³C=–5; and rare prehnite-chlorite lined fractures formed at 250 to 290° C. A generation of adularia-bearing veins precipitated at 140 to 230° C, from CaCl₂-NaCl brines, where ¹⁸O=0 to –6.5 and D=–10 to –30. Incremental ⁴⁰Ar/³⁹Ar age spectra on the K-feldspar yield an upper plateau of 1100 Ma. Subsequently, hematite developed during reactivation of earlier fractures, at 140 to 210° C in the presence of fluids characterized by ¹⁸O=–0.4 to –5.4 and D=–15 to –25. Arrays of open fractures partially occupied by gypsum and goethite reflect a fluid infiltration event at temperatures <50° C. Many of the earlier generations of fracture minerals have transgranular fracture infillings which record the presence of low temperature (88–190° C), hypersaline CaCl₂-NaCl brines. Narrow fractures lined with clays±calcite are sites for seepage of modern ground-waters. The isotopic signature of clay ( ¹⁸O=12 to 20, D=–80±5) plots near the line for modern kaolinites, confirming its formation in the presence of recent surface waters. Calcites coexisting with the clay minerals, and in fractured pegmatite show a common isotopic signature ( ¹⁸O=23±0.5, ¹³C=–13.6), indicating precipitation from modern groundwaters, where reactivated fractures have acted as conduits for infiltration of surface waters to depths of 200 m. Intermittent fracture-infiltration has occurred over 2.7 Ga. The early sequences of fracture-related fluid flow are interpreted in terms of devolatilization of the granite, followed by thermal contraction fracturing, incursion of marine water and convective cooling in the Archean. Hematite and adularia fracture fillings correspond to a stage when meteoric water infiltrated the volcanicplutonic terrain during Proterozoic and later times. Episodic fracture-fluid expulsion events may have been driven by seismic pumping, in response to magmatically and tectonically induced stresses within the Shield, with surface waters penetrating to depths of 15 km in the crust.     

Sulphur and sulphate-oxygen isotopes and the origin of the silvermines deposits,Ireland

New sulphur and sulphate-oxygen isotope measurements for the main discordant and stratiform lead-zinc-barite orebodies at Silvermines Co. Tipperary, allow reappraisal of previously offered differing interpretations (Graham, 1970; Greig et al., 1971) of the bearing of sulphur isotopes on the genesis of this important Irish deposit. The following aspects of the data are confirmed: barite ³⁴ S-values range from 17–21, similar to lower Carboniferous seawater sulphate: stratiform sulphide lens pyrites have ³⁴ S-values ranging from –13 to –36; vein sulphide ³⁴ S-values range from –8 to 4; sulphide ³⁴ S-values increase upwards and outwards respectively in the related discordant and stratiform G orebodies; galena-sphalerite isotope palaeotemperatures are not too consistent, ranging from 40 to 430°C (using the calibration of Czamanske and Rye (1974). New facts are as follows: barite ¹⁸O-values range from –13 to –17, stratiform barites ranging from 13 to 14.5; sulphides separated from a single stratiform ore lens hand specimen usually have ³⁴ S_sl > ³⁴ S_ga > ³⁴ S_py; the outward decrease in ³⁴ S-values in the stratiform G orebody is confined to the first few hundred feet only; pyrite ³⁴ S-values progressively increase downwards through one stratiform sulphide orebody; yet variations of 13 occur within a single colloform pyrite structure from another stratiform orebody. It is concluded that there were at least two sources of sulphur, seawater sulphate and deep-seated sulphur. The former was the dominant source of all sulphate and, via biogenic reduction, of the sulphur in the bulk of the stratiform sulphide. The latter was the source of the sulphur in the vein sulphides. There was minimal isotopic interaction between the cool seawater sulphate and the warm unwelling ore fluid sulphur species, even though the latter precipitated under near isotopic equilibrium conditions when the temperature dropped and/or the pH and Eh increased. The lack of isotopic equilibrium between pyrite and ore sulphides in the stratiform ore lenses may result from the latter having precipitated slightly later than the former because of solubility relationships. Overall the present isotopic evidence supports considerable geological evidence favoring a syngenetic origin for the stratiform Silvermines orebodies.     

An oxygen isotope study of the Loon Lake pluton and the Apsley gneiss,Ontario

The Loon Lake pluton in the Grenville province of Southeastern Ontario consists of a quartz monzonite rim surrounding a monzonite core containing inclusions of gneiss, gabbro and diorite. The pluton was emplaced in amphibolite facies Apsley gneiss, amphibolite and marble. Abnormally high ¹⁸O values are observed in all igneous rock types: quartz monzonite (8.9–13.9), monzonite (8.9–9.7), diorite-gabbro (8.0–9.3). High ¹⁸O contents are attributable to interaction between pluton and country rocks, through either isotopic exchange or direct mixing of mobilizate anatectically produced in the contact aureole of the pluton.The Apsley gneiss displays a ¹⁸O range from 8.3 to 16.9. There is no difference in ¹⁸O distribution between rocks inside and outside the contact aureole, although intermineral isotopic fractionations in the aureole are smaller than those outside. A chemical composition discriminant function that distinguishes rocks of igneous origin (DF>0) from sedimentary (DF<0) is inversely correlated with ¹⁸O of the gneisses, indicating that low ¹⁸O values are inherited from a silicic volcanic protolith. Al₂O₃/Na₂O, an index of maturity of sediments, increases with ¹⁸O for the DF<0 group but is almost constant for the DF>0 group over a ¹⁸O range from 8.3 to 13.4. The DF<0 group is inferred to have formed from a series of clastic sediments of varying degree of weathering or maturity; the DF>0 group formed either from tuffs partially altered to zeolites, or from hydrated volcanic flows or ignimbrites.     

Oxygen isotope geochemistry of hydrothermally-altered synmetamorphic granitic rocks from South-Central Maine,USA

Hydrothermally-altered mesozonal synmetamorphic granitic rocks from Maine have whole-rock ¹⁸O (SMOW) values 10.7 to 13.8. Constituent quartz, feldspar, and muscovite have ¹⁸O in the range 12.4 to 15.2, 10.0 to 13.2, and 11.1 to 12.0, respectively. Mean values of _Q–F ( ¹⁸O_quartz– ¹⁸O_feldspar)=2.4 and _Q–M ( ¹⁸O_quartz– ¹⁸O_muscovite)=3.3 are remarkably uniform (standard deviations of both are 0.2). Measured _Q–F and _Q–M values demonstrate that the isotopic compositions of the minerals are altered from primary magmatic ¹⁸O values but that the minerals closely approached oxygen isotope exchange equilibrium at subsolidus temperatures. Analyzed muscovites have D (SMOW) values in the range –65 to –82.Feldspars in the granitic rocks are mineralogically altered to either (a) muscovite+calcite, (b) muscovite+calcite+epidote, (c) muscovite+epidote, or (d) muscovite only. A consistent relation exists between the assemblage of secondary minerals and the oxygen isotope composition of whole rocks, quartz, and feldspar. Rocks with assemblage (a) have whole-rock ¹⁸O>12.1 and contain quartz and feldspar with ¹⁸O>13.8 and >11.4, respectively. Rocks with assemblages (b), (c), and (d) have whole-rock ¹⁸O<11.4 and contain quartz and feldspar with ¹⁸O< 13.1 and <11.0, respectively. The correlation suggests that the mineralogical alteration of the rocks was closely coupled to their isotopic alteration.Three mineral thermometers in altered granite suggest that the hydrothermal event occurred in the temperature range 400°–150° C, 100°–150° C below the peak metamorphic temperature inferred for country rocks immediately adjacent to the plutons. Calculations of mineral-fluid equilibria indicate that samples with assemblage (a) coexisted during the event with CO₂-H₂O fluids of and ¹⁸O=10.8 to 12.2 while samples with assemblages (b), (c), or (d) coexisted with fluids of and ¹⁸O=9.4 to 10.1. Compositional variations of the hydrothermal fluids were highly correlated: fluids enriched in CO₂ were also enriched in ¹⁸O. Because CO₂ was added to the granites during hydrothermal alteration and because fluids enriched in CO₂ were enriched in ¹⁸O, some or all of the variation in ¹⁸O of altered granites may have been caused by addition of ¹⁸O to the rocks during the hydrothermal event. The source of both the CO₂ and ¹⁸O could have been high-¹⁸O metasedimentary country rocks. The inferred change in isotopic composition of the granites is consistent with depletion of the metacarbonate rocks in ¹⁸O close to the plutons and with large volumes of fluid that were inferred from petrologic data to have infiltrated the metacarbonate rocks during metamorphism.A close approach of minerals to oxygen isotope exchange equilibrium in altered mesozonal rocks from Maine is in marked contrast to hydrothermally-altered epizonal granites whose mineral commonly show large departures from oxygen isotope exchange equilibrium. The difference in oxygen isotope systematics between altered epizonal granites and altered mesozonal granites closely parallels a differences between their mineralogical systematics. Both differences demonstrate the important control that depth exerts on the products of hydrothermal alteration. Deeper hydrothermal events occur at higher temperature and are longer-lived. Minerals and fluid have sufficient time to closely approach both isotope exchange and heterogeneous chemical equilibrium. Shallower hydrothermal events occur at lower temperatures and are shorter-lived. Generally there is insufficient time for fluid to closely approach equilibrium with all minerals.     

Stable isotope (C,O, S) systematics of the mercury mineralization at Idrija,Slovenia: constraints on fluid source and alteration processes

The world-class Idrija mercury deposit (western Slovenia) is hosted by highly deformed Permocarboniferous to Middle Triassic sedimentary rocks within a complex tectonic structure at the transition between the External Dinarides and the Southern Alps. Concordant and discordant mineralization formed concomitant with Middle Triassic bimodal volcanism in an aborted rift. A multiple isotopic (C, O, S) investigation of host rocks and ore minerals was performed to put constraints on the source and composition of the fluid, and the hydrothermal alteration. The distributions of the ¹³C and ¹⁸O values of host and gangue carbonates are indicative of a fracture-controlled hydrothermal system, with locally high fluid-rock ratios. Quantitative modeling of the ¹³C and ¹⁸O covariation for host carbonates during temperature dependent fluid-rock interaction, and concomitant precipitation of void-filling dolomites points to a slightly acidic hydrothermal fluid (¹³C–4 and ¹⁸O+10), which most likely evolved during isotopic exchange with carbonates under low fluid/rock ratios. The ³⁴S values of hydrothermal and sedimentary sulfur minerals were used to re-evaluate the previously proposed magmatic and evaporitic sulfur sources for the mineralization, and to assess the importance of other possible sulfur sources such as the contemporaneous seawater sulfate, sedimentary pyrite, and organic sulfur compounds. The ³⁴S values of the sulfides show a large variation at deposit down to hand-specimen scale. They range for cinnabar and pyrite from –19.1 to +22.8, and from –22.4 to +59.6, respectively, suggesting mixing of sulfur from different sources. The peak of ³⁴S values of cinnabar and pyrite close to 0 is compatible with ore sulfur derived dominantly from a magmatic fluid and/or from hydrothermal leaching of basement rocks. The similar stratigraphic trends of the ³⁴S values of both cinnabar and pyrite suggest a minor contribution of sedimentary sulfur (pyrite and organic sulfur) to the ore formation. Some of the positive ³⁴S values are probably derived from thermochemical reduction of evaporitic and contemporaneous seawater sulfates.Editorial handling: P. Lattanzi     

Contrasting fluid/rock interaction between the Notch Peak granitic intrusion and argillites and limestones in western Utah: evidence from stable isotopes and phase assemblages

The Jurassic Notch Peak granitic stock, western Utah, discordantly intrudes Cambrian interbedded pure limestones and calcareous argillites. Contact metamorphosed argillite and limestone samples, collected along traverses away from the intrusion, were analyzed for ¹⁸O, ¹³C, and D. The ¹³C and ¹⁸O values for the limestones remain constant at about 0.5 (PDB) and 20 (SMOW), respectively, with increasing metamorphic grade. The whole rock ¹⁸O values of the argillites systematically decrease from 19 to as low as 8.1, and the ¹³C values of the carbonate fraction from 0.5 to –11.8. The change in ¹³C values can be explained by Rayleigh decarbonation during calcsilicate reactions, where calculated is about 4.5 permil for the high-grade samples and less for medium and low-grade samples suggesting a range in temperatures at which most decarbonation occurred. However, the amount of CO₂ released was not anough to decrease the whole rock ¹⁸O to the values observed in the argillites. The low ¹⁸O values close to the intrusion suggest interaction with magmatic water that had a ¹⁸O value of 8.5. The extreme lowering of ¹³C by fractional devolatilization and the lowering of ¹⁸O in argillites close to the intrusion indicates oxgen-equivalent fluid/rock ratios in excess of 1.0 and X(CO₂)_F of the fluid less than 0.2. Mineral assemblages in conjunction with the isotopic data indicate a strong influence of water infiltration on the reaction relations in the argillites and separate fluid and thermal fronts moving thru the argillites. The different stable isotope relations in limestones and argillites attest to the importance of decarbonation in the enhancement of permeability. The flow of fluids was confined to the argillite beds (argillite aquifers) whereas the limestones prevented vertical fluid flow and convective cooling of the stock.     

Seawater-sediment-basalt interactions: stable isotope (H,O) and elemental fluxes within the Ordovician volcano-sedimentary sequence of Erquy (Brittany,France)

The Ordovician volcano-sedimentary succession of Erquy (northern Brittany) is made of immature sediments thermally metamorphosed at the contact of intruding basic sills. Pillow lavas constitute the upper part of the sequence. The trace element geochemistry of sills and pillow lavas suggests that they were derived from a tholeiitic source located beneath a passive margin. This volcanic sequence was metamorphosed under low to moderate greenschist facies conditions. In this study the direction and amplitude of chemical and isotopic fluxes in the basalt-sediment-water system were established and the oxygen and hydrogen isotope compositions of the aqueous fluid that reacted with the volcanic rocks were characterized. Cationic thermometry on chlorites and isotopic thermometry on plagioclase-chlorite pairs indicate closure metamorphic temperatures in the range 200–250°C for the basaltic sills. Stable isotope compositions of iron-rich chlorites (¹⁸O-5.5; D from-60 to-50) and plagioclases (¹⁸O from +9 to +10) reveal that the source of the fluid was certainly seawater. The ¹⁸O variations within the sills are strongly correlated with the rate of progress of the main metamorphic reaction:clinopyroxene+plagioclase+ilmenite chlorite+albite+epidote+quartz+sphene that produced major element mobility at the scale of the volcanosedimentary sequence. Calculation of elemental fluxes by mass balance combined with oxygen isotopic compositions of basalts shows that the highest water-rock ratios (1) were at sill-sediment boundaries and within pillow lavas at the top of the pile. The volcanosedimentary sequence of Erquy was a net sink for Na and a source for Ca. No Mg uptake could be detected whereas the hydrothermal alteration of the sediments released Fe, Si, and K trapped by the volcanic rocks. The ¹⁸O value of the fluid reacting with sills appears to have shifted no more than +4 after percolation at low temperature through immature sediments (¹⁸O12). The Erquy volcano-sedimentary sequence represents a marine hydrothermal system dominated by low-temperature exchange which allowed a general ¹⁸O-enrichment of the volcanic rocks and a ¹⁸O-depletion of sediments.     

The genesis of emeralds and their host rocks from Swat,northwestern Pakistan: a stable-isotope investigation

Emerald deposits in Swat, northwestern Pakistan, occurring in talc-magnesite and quartz-magnesite assemblages, have been investigated through stable isotope studies. Isotopic analyses were performed on a total of seven emeralds, associated quartz (seven samples), fuchsite (three samples) and tourmaline (two samples) from the Mingora emerald mines. The oxygen isotopic composition ( ¹⁸O SMOW) of emeralds shows a strong enrichment in¹⁸O and is remarkably uniform at + 15.6 ± 0.4 (1,n = 7). Each of the two components of water in emerald (channel and inclusion) has a different range of hydrogen isotopic composition: the channel waters being distinctly isotopically heavier (D = –51 to –32 SMOW) than the other inclusion waters (D = –96 to –70 SMOW). Similarly the oxygen isotopic compositions of tourmaline and fuchsite are relatively constant ( ¹⁸O = + 13 to + 14 SMOW) and show enrichment in¹⁸O. The ¹⁸O values of quartz, ranging from + 15.1 to + 19.1 SMOW, are also high (+ 16.9 ± 1.4 1, n = 7). The meanD of channel waters measured from emerald (–42 ± 6.6 SMOW) and that of fluid calculated from hydrous mineralsD_calculated (–47 ± 7.1 SMOW) are consistent with both metamorphic and magmatic origin. However, the close similarity between the measuredD values of the hydroxyl hydrogen in fuchsite (–74 to –6 SMOW) and tourmaline (–84 and –69 SMOW) with pegmatitic muscovite and tourmaline suggests that the mineralization was probably caused by modified (¹⁸O-enriched) hydrothermal solutions derived from an S-type granitic magma. The variation in the carbon and oxygen isotopic composition of magnesite, locally associated with emerald mineralization, is also very restricted ( ¹³ –3.2 ± 0.7%, PDB; ¹⁸O + 17.9 ± 1.27 SMOW). On the basis of the isotopic composition of fluid ( ¹³C –1.8 ± 0.7 PDB; ¹⁸O + 13.6 ± 1.2 SMOW calculated for the 250-550 °C temperature), it is proposed that the Swat magnesites formed due to the carbonation of previously serpentinized ultramafic rocks by a CO₂-bearing fluid of metamorphic origin.     

Oxygen,sulfur, and strontium isotope and fluid inclusion studies of barite deposits from the Iglesiente-Sulcis mining district,Southwestern Sardinia,Italy

This paper deals with barite from stratiform, karst, and vein deposits hosted within Lower Paleozoic rocks of the Iglesiente-Sulcis mining district in southwestern Sardinia. For comparison sulfates from mine waters are studied. Stratiform barite displays ³⁴S=28.8–32.1, ¹⁸O=12.7–15.6, and ⁸⁷Sr/⁸⁶Sr=0.7087, in keeping with an essentially Cambrian marine origin of both sulfate and strontium. Epigenetic barite from post-Hercynian karst and vein deposits is indistinguishable for both sulfur and oxygen isotopes with ³⁴S=15.3–26.4 and ¹⁸O=6.6–12.5; ⁸⁷Sr/⁸⁶Sr ratios vary 0.7094–0.7140. These results and the microthermometric and salinity data from fluid inclusions concur in suggesting that barite formed at the site of mineralization by oxidation of reduced sulfur from Cambrian-Ordovician sulfide ores in warm, sometimes hot solutions consisting of dilute water and saline brine with different ¹⁸O values. The relative proportion of the two types of water may have largely varied within a given deposit during the mineralization. In the karst barite Sr was essentially provided by carbonate host rocks, whereas both carbonate and Lower Paleozoic shale host rocks should have been important sources for Sr of the vein barite. Finally, ³⁴S data of dissolved sulfate provide further support for the mixed seawater-meteoric water composition of mine waters from the Iglesiente area.     

Geochemische Characteristica mariner Einflüsse in Torfen und Anderen Quaternären Sedimenten

Zusammenfassung Am Beispiel noch nicht diagenetisch verfestigter junger Sedimente wird die Verteilung der Spurenelemente im Profil untersucht und ihre Beziehungen zu Faziesänderungen, plötzlichen oder langsamen Änderungen der Salinität des Sedimentationsbeckens festgestellt.

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The repartition of trace-elements in profiles of non consolidated quaternary sediments is given. It is possible to give an interpretation not only of the different facies, but also to study the more or less rapid changes of the salinity during the sedimentation.

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Résumé Sur des profils de sédiments récents non consolidés par diagenèse, l'auteur étudie la répartition des éléments en traces et les relations de leur distribution avec les changements de faciès —y inclus la détermination des variations plus ou moins rapides de la salinité du bassin de sédimentation.

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Die vorliegenden Untersuchungen wurden 1959 begonnen im mineralogischen Institut der Universität Hamburg; ich habe dem damaligen Institutsleiter, Herrn ProfessorDrescher-Kaden, zu danken für die gewährte Gastfreundschaft und der Deutschen Forschungsgemeinschaft für die finanzielle Unterstützung. Der Abschluß der Arbeiten erfolgte 1961 in Nancy während meiner Tätigkeit als Professeur Associé der Ecole Nationale Supérieure de Géologie Appliquée et de Prospection Minière, deren Direktor, Herrn Professor M.Roubault, ich ebenfalls sehr zu Dank verpflichtet bin.     

Invasion of anthropogenic CO<Subscript>2</Subscript> recorded in planktonic foraminifera from the northern Gulf of Aqaba

The stable carbon isotopic composition of the planktonic foraminifera Globigerinoides sacculifer and G. ruber (white) and sedimentary organic matter from the northern Gulf of Aqaba have been investigated to estimate changes in ¹³C_DIC in surface waters during the last 1,000 years. The high sedimentation rates at the core sites (about 54 cm/Kyear) provide high temporal resolution (~10 years). Recent sediments at the top of the cores reflect conditions younger than 1950. The ¹³C records of the planktonic foraminifera from three multicores display similar trends, showing a uniform and consistent pattern before the 1750s, and a gradual decrease of approximately 0.63 over the last two centuries. This decrease seems to track the decrease of ¹³C_DIC in surface waters, which is mainly caused by the increase of anthropogenic input of ¹³C-depleted CO₂ into the atmosphere. Similarly, a trend towards lighter values of the carbon isotopic composition of sedimentary organic matter (¹³C_org) during the last 200 years supports the interpretation obtained from the planktonic foraminiferal ¹³C. Furthermore, direct measurements of seawater show that ¹³C of the dissolved inorganic carbon (DIC) in the northern Gulf of Aqaba has decreased by about 0.44 during the period 1979–2000. The average annual decrease is 0.021, which is similar to that observed globally. The ¹³C values of planktonic foraminifera combined with organic matter ¹³C from marine sediments are good indicators for reconstructing past changes in atmospheric CO₂ concentrations from the northern Gulf of Aqaba.     

Oxygen and hydrogen isotope compositions of eclogites and associated rocks from the Eastern Sesia zone (Western Alps,Italy)

Oxygen and hydrogen isotope analyses have been made of mineral separates from eclogites, glaucophanites and glaucophane schists from the eastern Sesia zone (Italian Western Alps). Regularities in (1) hydrogen isotope compositions, (2) order of ¹⁸O enrichment among coexisting minerals, and (3) ¹⁸O (quartz-rutile) and ¹⁸O (quartz-phengite) imply attainment of a high degree of isotopic equilibrium. However, some scattering of ¹⁸O values of individual minerals indicates that the eclogitic assemblage did not form in the presence of a thoroughly pervasive fluid. Minerals from an eclogitic lens enclosed in marble have ¹⁸O values distinctly different from those measured in the other rocks. The ¹⁸O values are high in comparison with other type C eclogites of the world, and it is proposed that the fluid present during the high pressure metamorphism has to a large extent been inherited from the precursor rocks of amphibolite facies.An average formation temperature of 540 ° C is inferred from the oxygen isotope fractionations between quartz and rutile and between quartz and white mica. This temperature is in accordance with petrologic considerations and implies subduction of the precursor rocks into the upper mantle to achieve the high pressures required.     

Evidenzen für die Vergletscherung eines alpinen Bergeller Hochgebirges an der Grenze Oligozän/Miozän

Zusammenfassung Aus fossilen Floren abgeleitete paläoklimatische und -ökologische Daten, Geröllanalysen und Alters-, insbesondere Spaltspur-Daten aus der südalpinen Molasse und vom Bergeller Pluton erlauben den Zusammenhang zwischen Vorland und alpinem Relief zu gewinnen. Die Zusammenfassung aller Daten und Evidenzen bringt uns zu folgender Vorstellung:Im jüngsten Oligozän haben sich im bis über 5000 m emporgestiegenen Bergeller Hochgebirge Gletscher gebildet. Dies war möglich, da während der gleichzeitigen Klima-Depression die Temperaturen kaum höher waren als heute. Die häufig facettierten Blöcke von vorwiegend Bergeller Material wurden weitgehend auf einem Gletscher nach Süden transportiert, allein die letzte Wegstrecke muß durch Schichtfluten erfolgt sein; diese sind auf sich wiederholende Dammbrüche von Moränenwällen zurückzuführen, die in vorgezeichneten Tälern Seen aufstauten.Die extreme Frische der Gesteine, von den großen Blöcken bis zum feinen Grus, deutet darauf hin, daß der Transport in relativ kurzer Zeit und bei relativ tiefer Temperatur, wie sie der Gletscher bietet, erfolgte.

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Based on paleobotanic and paleoecologic data, boulder analyses as well as geochronological data, especially fission track ages on Bergell rocks from the Alps and the molasse boulders, it has been possible to reconstruct the connection between the Alpine relief and the foreland. Summarizing all facts and evidence leads to the following model: At the end of Oligocène time the Bergell mountains with altitudes above 5000 m were glaciated, because at this time the temperature was not much higher than the present day temperature. The often wellfacetted boulders have been carried to the south to the main part by the glacier; only the last part of the transport has been effected by floods, due to ruptures of moraines which dammed lakes in preformed valleys. All the rocks in the molasse near Como, the big boulders as well as the finer debris, are extremely fresh, a strong argument for quick transport at low temperature.

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Résumé Les résultats paléoclimatiques et -écologiques livrés par les flores fossiles, les analyses de galets, les dates de traces de fission dans les galets de la molasse sudalpine et du massif du Bergell permettent d'établir la liaison entre le relief alpin et celui de l'avant-pays. En résumant les dates et les évidences nous arrivons à la conclusion suivante: à la fin de l'Oligocène des glaciers s'étaient formés dans les hautes montagnes brégagliennes atteignant plus de 5000 m. Les températures de cette dépression climatique, à peine plus hautes que celles de notre époque, expliquent ce phénomène. Les blocs, souvent facettés, en provenance de ce massif cristallin, prédominent et furent transportés par un glacier vers le sud; seul le dernier parcours s'effectua par des coulées, dues à des ruptures de barrages morainiques dans les vallées préformées. L'extraordinaire état de conservation des roches, comportant des blocs jusqu'à un matériel fin, indique un transport en un court laps de temps et dans des conditions de basses températures comme celles produites par un glacier.

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, - . : , 5.000 , . , - . , , , ; , . .

     

Bimodal early proterozoic volcanism in the Grythytte field and associated volcano-plutonic complexes,Bergslagen, Central Sweden

The Grythytte field sequence forms a NNW belt of acid-basic metavolcanic and metasedimentary rocks. The geology shows characteristics of a dynamic process of trough-forming and infilling which to a large extent post-dates the Hjulsjö volcanoplutonic complex situated to the east. In the latter complex acid metapyroclastics strike around a centre of granite and granophyre, which cut and are cut by basic sills and dykes. Field and petrochemical evidence points to a distinct bimodal magmatism that ist manifested during one short phase of a rifting period.

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Zusammenfassung Die Grythytte Schichtenfolge bildet einen NNW verlaufenden Gürtel aus sauren und basischen Metavulkaniten und Metasedimenten. Die geologischen Befunde weisen auf einen dynamischen Entstehungsprozeß von Grabenbildung und Füllung hin. Im weiter östlich gelegenen vulkanisch-plutonischen Hjulsjö-Komplex streichen älteren metamorphen pyroklastischen Gesteine rund ein Granit-Granophyr Zentrum. Dieser Komplex durchschneidet und wird durchschnitten von basischen Sills und Gängen. Feldgeologische und geochemische Untersuchungen weisen deutlich auf einen bimodalen Magmatismus hin, der während einer kurzen Phase der Grabenbildung stattfand.

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Résumé La séquence de Grythytte forme une ceinture de roches métavolcaniques et métasédimentaires de direction NNO. La géologie fait apparaître les caractéristiques d'un processus dynamique de formation de fosse et de remplissage, qui s'est produit, pour la plus grande partie, après la formation du complexe volcano-plutonique de Hjulsjö situé à l'Est. Dans ce dernier complexe des produits pyroclastiques acides sont disposés autour d'un centre granitoïde et granophyrique, qui à son tour recoupe et est recoupé par des sills et des dykes basiques. Les observations de terrain et les faits pétrochimiques indiquent un procèssus magmatique distinctement bimodal qui s'est manifesté pendant une phase courte dans une période de «rifting».

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Grythytte , NNW . . Hjulsj -- . . , , .

     

Sulfur isotope ratios of Icelandic rocks

Sulfur isotope ratios have been determined in 27 selected volcanic rocks from Iceland together with their whole rock chemistry. The ³⁴S of analyzed basalts ranges from –2.0 to +0.4 with an average value of –0.8 Tholeiitic and alkaline rocks exhibit little difference in ³⁴S values but the intermediate and acid rocks analyzed have higher ³⁴S values up to +4.2 It is suggested that the overall variation in sulfur isotope composition of the basalts is caused by degassing. The small range of the ³⁴S values and its similarity to other oceanic and continental basalts, suggest that the depleted mantle is homogeneous in its sulfur isotope composition. The ³⁴S of the depleted mantle is estimated to be within the range for undegassed oceanic basalts, –0.5 to +1.0     

Wechselbeziehung kaledonischer Deformationspläne nordöstlich Stavanger (Südwest-Norwegen)

Zusammenfassung Zur Ergänzung der petrographischen Neuaufnahme des kaledonischen Gebirges nordöstlich Stavanger durchGeorg Müller wurde eine strukturgeologische Felduntersuchung vorgenommen.Die obersten Partien des Präkambriums und die metamorphe Gesteinsserie des Kambro-Silurs zeigen zwei Deformationspläne, die sich aufgrund ihrer Altersbeziehungen, ihres Deformationsstils und der vorherrschenden Achsenrichtungen deutlich voneinander unterscheiden. Sie sind daher das Ergebnis zweier unabhängiger Deformationsphasen.Die ältere Deformation (F1) hat mit wechselnder Stärke den gesamten Bereich erfaßt. Ihre Faltenachsen zeigen überwiegend Nordwest-Südost-Richtung. Charakteristisch ist Isoklinalfaltung.Die jüngere Deformationsphase (F2) zeigt keinen ausgeprägten Faltungsstil und hat sich vor allem im unteren Teil der kambro-silurischen Gesteinsserie ausgewirkt. Bei den Faltenachsen überwiegt die Nordost-Südwest-Richtung.Das Quarzkorngefüge hat während der F 1-Deformation eine starke Regelung erfahren. Dagegen hat nur sehr intensive F 2-Faltung zu einer Umregelung geführt.

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In order to complete the petrographic mapping of the Caledonian mountains NE of Stavanger by G.Müller, the structural geology was again studied in the field.The upper parts of the Precambrien and the metamorphic rocks of the Cambro-Silurien show two different deformation plans, which may be distinguished clearly by their age, their style of deformation and the predominant orientation of their axes. Therefore, they were originated in two independent deformation phases.The older deformation (F 1) influenced the complete area with changing intensity. Their fold axes show mostly to NW-SE. Isoclinal folds seem to be characteristic.The younger deformation (F2) does not show a typical style of folding. It influenced especially the lower part of the Cambro-Silurian series. The orientation of the fold axes points especially to NE-SW.The orientation of the quartz axes was regulated parallel during the F 1-deformation. Only heavy F 2-folding led to reorientation of the axes.

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Résumé Dans le but de compléter les nouveaux levés pétrographiques de la chaîne calédonienne au nord-est de Stavanger réalisés par G.Müller, l'auteur a entrepris des travaux de terrain au point de vue structural.Les parties supérieures du Précambrien et la série de roches métamorphiques du Cambro-Silurien montrent deux systèmes de déformation, qui se différencient nettement par leur âge, le style de leur déformation et leurs directions axiales prédominantes, Elles résultent donc de deux phases de déformation indépendantes l'une de l'autre.La phase de déformation la plus ancienne (F1) a touché avec une violence plus ou moins forte l'ensemble du domaine. Les axes de plissement prennent principalement la direction nord-ouest/sud-est. Son plissement isoclinal est très caractéristique.La phase de déformation plus jeune (F 2) ne présente aucun style de plissement bien marqué et a agi principalement sur la partie inférieure de la série de roches cambro-siluriennes. Les axes de plissement sont surtout dirigés nord-est/sud-ouest.Les grains de quartz ont été soumis à une forte régulation pendant la première phase de déformation (F1). Par contre c'est uniquement là où le plissement a été très intense au cours de la deuxième phase (F 2) que le quartz a pris une nouvelle structure.

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Stavauger, Georg üll', . , . , , . (F₁) . , . , NW-SE . . (F₂) , . ., - . , . ., NE-SW. F₁ . F₂ .

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Den Herren Professoren Dr. F.Karl, Kiel, und Dr. G.Müller, Clausthal, möchte ich hiermit für anregende Diskussionen und die gute Zusammenarbeit, Herrn Dr. G.Braun und Dr. A.Richter (beide Kiel) für die Mithilfe bei den Korngefügeanalysen danken. Der Deutschen Forschungsgemeinschaft bin ich für die Finanzierung der Untersuchungen — im Rahmen des Forschungsvorhabens Gesteinsmetamorphose — zu Dank verpflichtet.     

Stable isotope geochemistry of the Archean Val-d‘Or (Canada) orogenic gold vein field

A systematic study of the auriferous quartz veins of the Val-dOr vein field, Abitibi, Quebec, Canada, demonstrates that the C, O, S isotope composition of silicate, carbonate, borate, oxide, tungstate and sulphide minerals have a range in composition comparable to that previously determined for the whole Superior Province. The oxygen isotope composition of quartz from early quartz–carbonate auriferous veins ranges from 9.4 to 14.4 whereas later quartz-tourmaline-carbonate veins have ¹⁸O_quartz values ranging from 9.2 to 13.8 . Quartz-carbonate veins have carbonate (¹⁸O: 6.9–12.5 ; ¹³C: –6.2– –1.9 ) and pyrite (³⁴S: 1.2 and 1.9 ) isotope compositions comparable to those of quartz-tourmaline-carbonate veins (¹⁸O: 7.9–11.7 ; ¹³C: –8.0 – –2.4 ; ³⁴S: 0.6–6.0 ). ¹⁸O_quartz values in quartz-tourmaline-carbonate veins have a variance comparable to analytical uncertainty at the scale of one locality, irrespective of the type of structure, the texture of the quartz or its position along strike, across strike or down-dip a vein. In contrast, the oxygen isotope composition of quartz in quartz-tourmaline-carbonate veins displays a regional distribution with higher ¹⁸O values in the south-central part of the vein field near the Cadillac Tectonic Zone, and which ¹⁸O values decrease regularly towards the north. Another zone of high ¹⁸O values in the northeast corner of the region and along the trace of the Senneville Fault is separated by a valley of lower ¹⁸O values from the higher values near the Cadillac Tectonic Zone. Oxygen isotope isopleths cut across lithological contacts and tectonic structures. This regional pattern in quartz-tourmaline-carbonate veins is interpreted to be a product of reaction with country rocks and mixing between (1) a deep-seated hydrothermal fluid of metamorphic origin with minimum ¹⁸O=8.5 , ¹³C=0.6 and ³⁴S=–0.4 , and (2) a supracrustal fluid, most likely Archean seawater with a long history of water-rock exchange and with maximum ¹⁸O=3.9 , ¹³ C=–5.6 and ³⁴S=5.0 .