Ocean acidification in the aftermath of the Marinoan glaciation

Boron isotope patterns preserved in cap carbonates deposited in the aftermath of the younger Cryogenian (Marinoan, ca. 635 Ma) glaciation confirm a temporary ocean acidification event on the continental margin of the southern Congo craton, Namibia. To test the significance of this acidification event and reconstruct Earth’s global seawater pH states at the Cryogenian-Ediacaran transition, we present a new boron isotope data set recorded in cap carbonates deposited on the Yangtze Platform in south China and on the Karatau microcontinent in Kazakhstan. Our compiled δ11B data reveal similar ocean pH patterns for all investigated cratons and confirm the presence of a global and synchronous ocean acidification event during the Marinoan deglacial period, compatible with elevated postglacial pCO2 concentrations. Differences in the details of the ocean acidification event point to regional distinctions in the buffering capacity of Ediacaran seawater

Some applications of stable isotopes of carbon and oxygen in oceanography

Abstract available : p.[xvi-xvii

Duration and nature of the end-Cryogenian (Marinoan) glaciation

The end-Cryogenian glaciation (Marinoan) is portrayed commonly as the archetype of snowball Earth, yet its duration and character remain uncertain. Here we report U-Pb zircon ages for two ash beds from widely separated localities of the Marinoan-equivalent Ghaub Formation in Namibia: 639.29 ± 0.26 Ma and 635.21 ± 0.59 Ma. These findings verify, for the first time, the key prediction of the snowball Earth hypothesis for the Marinoan glaciation, i.e., longevity, with a duration of ≥4 m.y. They also show that the nonglacial interlude of Cryogenian time spanned 20 m.y. or less and that glacigenic erosion and sedimentation, and at least intermittent open-water conditions, occurred 4 m.y. prior to termination of the Marinoan glaciation

Fluid and metal sources in the Fäboliden hypozonal orogenic gold deposit, Sweden

To model the formation of orogenic gold deposits, in a global perspective, it is important to understand the ore-forming conditions not only for deposits hosted in greenschist facies rocks but also in amphibolite facies. The Paleoproterozoic Fäboliden deposit in northern Sweden belongs to the globally rare hypozonal group of orogenic gold deposits and, as such, constitutes a key addition to the understanding of amphibolite facies orogenic gold deposits. The Fäboliden deposit is characterized by auriferous arsenopyrite-rich quartz veins, hosted by amphibolite facies supracrustal rocks and controlled by a roughly N-striking shear zone. Gold is closely associated with arsenopyrite-löllingite and stibnite, and commonly found in fractures and as inclusions in the arsenopyrite-löllingite grains. The timing of mineralization is estimated from geothermometric data and field relations at c. 1.8 Ga. In order to constrain the origin of gold-bearing fluids in the Fäboliden deposit, oxygen, hydrogen, and sulfur isotope studies were undertaken. δ18O from quartz in veins shows a narrow range of + 10.6 to + 13.1‰. δD from biotite ranges between − 120 and − 67‰, with most data between − 95 and − 67‰. δ34S in arsenopyrite and pyrrhotite ranges from − 0.9 and + 3.6‰ and from − 1.5 and + 1.9‰, respectively. These stable isotope data, interpreted in the context of the regional and local geology and the estimated timing of mineralization, suggest that the sulfur- and gold-bearing fluid was generated from deep-crustal sedimentary rocks during decompressional uplift, late in the orogenic evolution of the area. At the site of gold ore formation, an 18O-enriched magmatic fluid possibly interacted with the auriferous fluid, causing precipitation of Au and the formation of the Fäboliden hypozonal orogenic gold deposit

Carbonate deposition in the Palaeoproterozoic Onega basin from Fennoscandia : a spotlight on the transition from the Lomagundi-Jatuli to Shunga events

Date of Acceptance: 08/05/2015 Date of online publication: 16/05/2015 Acknowledgements Elemental and isotopic data, thin and polished sections used in this contribution were obtained through two large umbrella-projects with grants provided by the Norwegian Research Council grant 191530/V30 to VAM and NERC grant NE/G00398X/1 to AEF. We thank A. Črne, the editor A. Strasser as well as one anonymous reviewer and D. Papineau for providing their valuable criticism and suggestions.Peer reviewedPostprin

The Palaeoproterozoic global carbon cycle : insights from the Loch Maree Group, NW Scotland

Fieldwork was supported by the Edinburgh Geological Society Clough & Mykura Fund, the Carnegie Undergraduate Scholarship and a stipend provided by the Irvine Bequest through the University of St Andrews to G.B.K. Laboratory work, and isotope and geochronology analyses were financed by NERC grant NE/G00398X/1 to A.R.P., A.E.F., D.J.Condon and A.P.M. Thanks go to T. Donnelly, J. Dougans, A. Calder, D. Herd, B. Pooley and A. Mackie for laboratory assistance.Peer reviewedPostprin

High and intermediate sulphidation environment in the same hydrothermal deposit: the example of Au-Cu Palai–Islica deposit, Carboneras (Almería)

Two epithermal environments have been identified in the Miocene Palai–Islica Au–Cu deposit: A) Intermediate sulphidation, hosted mainly in quartz veins, comprises pyrite, chalcopyrite, sphalerite and galena as the major sulphides, which are accompanied by a variety of Ag-bearing accessory minerals. Au–Ag alloys are the only gold-bearing phase. The veins are enclosed by sericitic and chloritic alteration. Fluid inclusions in quartz, sphalerite and calcite give Th between 118–453 ºC, and salinities between 0.2–51.4 wt.% NaCl eq, with high salinities being related to high-grade mineralisation. Stable isotopes indicate magmatic and marine fluids. B) High sulphidation consists of massive host rock silicification with disseminated pyrite and minor chalcocite, covellite, native copper and native gold. The surrounding alteration is advanced argillic/argillic in style. Fluids have Th between 224–381 ºC have salinities between 0.4 and 41.1 wt.% NaCl eq. The stable isotope data demonstrate the dominance of magmatic fluids, and disproportion processesUniversidad de Granada. Departamento de Mineralogía y PetrologíaGrupo de Investigación de la Junta de Andalucía RNM-0131.Instituto Andaluz de Ciencias de la Tierra (CSIC-UGR)The research has been supported by the project BTE 2001-3308 of DGI of Ministerio de Ciencia y Tecnología of Spain and the RNM 0131 Research Group of Junta de Andalucía. AJB is funded by NERC support of the Isotope Community Support Facility at SUERC

Stable isotope evidence for near-surface, low-temperature formation of Mg-(hydro)carbonates in highly altered Greek Mesozoic serpentinites

Authigenic magnesite, hydromagnesite and huntite associated with intensely altered and serpentinized ophiolitic rocks in Attica (mainland Greece) occur predominantly as veinlets and nodules within a totally weathered former-serpentinite groundmass. Carbonate δ18O values are consistent with post-geothermal fluid temperatures between 25-70 ˚C, but mostly between 25-30 ˚C, from a dominantly meteoric-sourced groundwater, indicating near-surface, low-temperature conditions. Despite the proximity of a volcanic centre with strong CO2 flux, 75% of the carbon isotope data imply little or no incorporation of this CO2 into the authigenic Mg-(hydro)carbonates. Indeed, many δ13C values are more negative than soil-zone calcrete values, and in this setting Mg-(hydro)carbonate δ13C below -6‰ VPDB probably indicate disequilibrium effects in alkaline groundwaters. Geothermal fluids and groundwaters were mainly routed through structural conduits. Some of the low temperature hydromagnesite subsequently dehydrated to magnesite under near-surface conditions, while huntite is likely a diagenetic transformation of hydromagnesite, forming close to the volcanic centre where fluid Mg/Ca ratios were low. The isotopic signatures are distinct from previously published Balkan-East Mediterranean magnesite data arrays but are consistent with many other ultramafic-associated magnesium carbonates worldwide; their association with likely fluid compositions provide important context for Mg-(hydro)carbonate formation as geothermal conditions cool to near surface temperatures

Fractionation of rare earth elements in greisen and hydrothermal veins related to A-type magmatism

This study focuses on concentrations and fractionation of rare earth elements (REE) in a variety of minerals and bulk materials of hydrothermal greisen and vein mineralization in Paleoproterozoic monzodiorite to granodiorite related to the intrusion of Mesoproterozoic alkali- and fluorine-rich granite. The greisen consists of coarse-grained quartz, muscovite, and fluorite, whereas the veins mainly contain quartz, calcite, epidote, chlorite, and fluorite in order of abundance. A temporal and thus genetic link between the granite and the greisen/veins is established via high spatial resolution in situ Rb-Sr dating, supported by several other isotopic signatures (δ34S, 87Sr/86Sr, δ18O, and δ13C). Fluid-inclusion microthermometry reveals that multiple pulses of moderately to highly saline aqueous to carbonic solutions caused greisenization and vein formation at temperatures above 200–250°C and up to 430°C at the early hydrothermal stage in the veins. Low calculated ∑REE concentration for bulk vein (15 ppm) compared to greisen (75 ppm), country rocks (173–224 ppm), and the intruding granite (320 ppm) points to overall low REE levels in the hydrothermal fluids emanating from the granite. This is explained by efficient REE retention in the granite via incorporation in accessory phosphates, zircon, and fluorite and unfavorable conditions for REE partitioning in fluids at the magmatic and early hydrothermal stages. A noteworthy feature is substantial heavy REE (HREE) enrichment of calcite in the vein system, in contrast to the relatively flat patterns of greisen calcite. The REE fractionation of the vein calcite is explained mainly by fractional crystallization, where the initially precipitated epidote in the veins preferentially incorporates most of the light REE (LREE) pool, leaving a residual fluid enriched in the HREE from which calcite precipitated. Fluorite occurs throughout the system and displays decreasing REE concentrations from granite towards greisen and veins and different fractionation patterns among all these three materials. Taken together, these features confirm efficient REE retention in the early stages of the system and minor control of the REE uptake by mineral-specific partitioning. REE-fractionation patterns and fluid-inclusion data suggest that chloride complexation dominated REE transport during greisenization, whereas carbonate complexation contributed to the HREE enrichment in vein calcite

New insights on mineralogy and genesis of kaolin deposits: The Burela kaolin deposit (Northwestern Spain)

The Burela deposit is the largest kaolin deposit in Spain, mined for more than 50 years, the product being mainly used for porcelain. Kaolin is dominantly associated with Lower Cambrian felsites, interbedded with quartzites, micaschists and metapelites (Cándana Series), and was strongly folded during the Variscan orogeny. Kaolin layers were ductile and incompetent materials among more competent ones, producing many slides with a diastrophic appearance. Consequently, kaolin outcrops are morphologically very variable– i.e. pockets – and interlayered between metapelites and/or quartzites, resulting in complication for prospection and mining. The kaolin consists mainly of kaolinite, tubular halloysite, and spherical allophane along with quartz and minor illite. The content of kaolin minerals reaches up to 90% in the finer fractions (< 2 μm and < 1 μm). Geochemical analyses of trace and REE show a close relationship between kaolin and associated rocks. Two kaolin types can be differentiated: (i) massive, associated to felsite; and (ii) related to metapelite. A temperature range from 15 to 35 °C, with an average of approximately 28 °C was calculated on the basis of the isotopic signatures (δ18O, δD) for the kaolin materials. This scatter suggests that if continental weathering was involved in the kaolin formation on the lower side of the temperatures, it was not the only process, especially for kaolin associate with felsites and metapelites. The higher temperatures are indicative of a hydrothermal auto-metamorphic alteration, followed by a folding of the series that induced an apparently chaotic kaolin distribution with a combined continental weathering superimposed on the previous low-temperature hydrothermal felsite transformation