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Stable isotope (δ18O, δD) composition of magmatic fluids exsolved from an active alkaline magma chamber—the case of the AD 79 magma chamber of Vesuvius
Get PDFThis work documents, for the first time, the calculated oxygen and hydrogen isotope composition of the brines exsolved from the peripheral margin of the active magma alkaline chamber that fed the AD 79 (“Pompei”) eruption of Vesuvius. The exsolved hydrosaline fluids had a constant δ18O composition and a variable δD composition, showing a general lowering of δD at nearly constant δ18O content. We argue that the progressive fluid exsolution at the upper peripheral parts of the AD 79 magma chamber may explain this isotopic path. The modeling of the evolution of the hydrogen isotope composition of water remaining dissolved in the melt, and of the exsolved fluid as a consequence of progressive degassing, would favor multiple fluid-release events from the magmatic reservoir. A schematic model on the pulsed accumulation and release of fluids at the top of the magmatic reservoir prior to the eruption is thus proposed. The assessment of the stable isotope composition of the fluids exsolved from the AD 79 magma chamber of Vesuvius may be particularly relevant for the geochemical surveillance of the volcano as it may help to interpret the isotopic composition of fumarolic gases and its variations
Fluids in early stage hydrothermal alteration of high-sulfidation epithermal systems: A view from the Vulcano active hydrothermal system (Aeolian Island, Italy)
No full textHigh-sulfidation (HS) epithermal systems have elements in common with passively degassing volcanoes associated with high T,
acid fumarole fields or acid crater lakes. They are considered to form in two stages, the first of which involves advanced argillic
alteration resulting from intense, strongly acidic fluid–rock interaction. The La Fossa hydrothermal system (Vulcano Island)
represents a classic example of such an active HS system and can be considered as a modern analogue of this early stage of
alteration, resulting in a core of intense silicic (90–95% pure SiO2) alteration surrounded by alunitic alteration zones.
This paper focuses on a geochemical and stable isotope study of the surficial alteration facies of Vulcano – particularly the horizon
characterized by strong silicic alteration – and on deep seated xenoliths ejected during the last eruption of La Fossa volcano (1888–90)
that can be considered as representative of fragments of the deep conduit system of La Fossa volcano. Using directly measured
temperatures at the sites of sampling, we have calculated fluid composition in isotopic equilibrium with the alteration products. The
large range of measured silica δ18O (12.3 to 29‰) reflects the wide range of formation temperatures (80–240 °C). The fluid
compositions calculated for intense silicic alteration vary from −0.9 to +6.5‰. These are significantly heavier than local meteoric
water (−6‰), and are consistent with derivation from the condensation of high-temperature fumarolic gases, dominated by magmatic
fluids and rich in acid gases (SO2, H2S, HCl, HF), into shallow groundwaters of meteoric origin, with dynamically variable ratios of
fumarolic steam/meteoric water. The calculated δ18O and δD of water in equilibrium with alunite also suggest the mixing of magmatic
and meteoric waters for the fluids involved in the genesis of advanced argillic alteration facies.
The calculated δ18Oofwater in equilibrium with hedenbergitic clinopyroxene, found in a veinlet in ametasomatized xenolith is +8.9‰.
This value cannot reasonably result from water–rock interaction between the host volcanic rocks and surface water. Instead, it most likely
represents a fluid (brine) exsolved from magma, which was responsible for high temperature metasomatism in the deep conduit system.
© 2007 Elsevier B.V. All rights reserved
Minor Elements in Layered Sphalerite as a Record of Fluid Origin, Mixing, and Crystallization in the Navan Zn-Pb Ore Deposit, Ireland
No full textThis study tests the utility of the minor to trace element composition of sphalerite to discriminate between possible sources of ore-forming fluids, and to constrain processes involved in ore genesis of the world-class Irish-type Navan Zn-Pb orebody, Ireland. Detailed petrography and electron microprobe microanalyses were performed on layered sphalerite previously analyzed for Zn, Fe, and S isotope compositions. Layered sphalerite displays a wide range of chemical composition at both sample and crystal scales. The color, style, and scale of layering show variations with chemical composition, but none of these correlations are consistent between samples. However, there are strong intersample correlations between chemical and S-Fe-Zn isotope compositions at the millimeter scale. Sphalerite precipitated from deep, hydiothermal fluids with S-34-enriched sulfide is enriched in Cd, Sb, Cu, and Ag, whereas Fe and As are enriched in sphalerite precipitated from shallow, bacteriogenic brines with isotopically light S. Significant chemical variations also occur at the micrometer scale in sphalerite regardless of its genetic affinity. These variations are interpreted as being due to variations in temperature, pH, and sulfur activity following the arrival at the site of deposition of pulses of hydrothermal fluids at specific stages of sphalerite growth. Therefore the chemistry of sphalerite, coupled with its texture, appears to be a powerful tool to elucidate fluid typing and ore genesis. The results support the hypothesis that layered sphalerite forms by rapid crystallization due to mixing of two fluids of contrasting physicochemical properties, a process required for the formation of Irish-type and some other hydrothermal deposits including, most notably, Mississippi Valley-type (MVT) deposits. The existence of layered sphalerite, coupled with its texture and chemical composition, may therefore provide useful insight for the mineral exploration industry in Ireland and elsewhere
Rhenium enrichment in the Muratdere Cu-Mo (Au-Re) porphyry deposit, Turkey: evidence from stable isotope analyses (δ34S, δ18O, δD) and LA-ICP-MS analysis of sulfides
Get PDFThe Muratdere Cu-Mo (Au) porphyry deposit in western Turkey contains elevated levels of rhenium and is hosted within granodioritic intrusions into an ophiolitic mélange sequence in the Anatolian belt. The deposit contains several stages of mineralization: early microfracture-hosted molybdenite and chalcopyrite, followed by a quartz-pyrite-chalcopyrite vein set associated with Cu-Au grade, a quartz-chalcopyrite-pyrite-molybdenite vein set associated with Cu-Mo-Re grade, and a later polymetallic quartz-barite-sphalerite-galena-pyrite vein set. The rhenium in Muratdere is hosted within two generations of molybdenite: early microfracture-hosted molybdenite and later vein-hosted molybdenite. In situ laser ablation-inductively coupled plasma-mass spectrometry analysis of sulfides shows that the later molybdenite has significantly higher concentrations of Re (average 1,124 ppm, σ = 730 ppm, n = 43) than the early microfracture-hosted molybdenite (average 566 ppm, σ = 423 ppm, n = 28). Pyrite crystals associated with the Re-rich molybdenite have higher Co and As concentrations than those in other vein sets, with Au associated with As. The microfracture-hosted sulfides have δ34S values between −2.2‰ and +4.6‰, consistent with a magmatic source. The vein-hosted sulfides associated with the high-Re molybdenite have a δ34S signature of 5.6‰ to 8.8‰, similar to values found in peridotite lenses in the Anatolian belt. The later enrichment in Re and δ34S-enriched S may be sourced from the surrounding ophiolitic country rock or may be the result of changing redox conditions during deposit formation
Minor Elements in Layered Sphalerite as a Record of Fluid Origin, Mixing, and Crystallization in the Navan Zn-Pb Ore Deposit, Ireland
No full textThis study tests the utility of the minor to trace element composition of sphalerite to discriminate between possible sources of ore-forming fluids, and to constrain processes involved in ore genesis of the world-class Irish-type Navan Zn-Pb orebody, Ireland. Detailed petrography and electron microprobe microanalyses were performed on layered sphalerite previously analyzed for Zn, Fe, and S isotope compositions. Layered sphalerite displays a wide range of chemical composition at both sample and crystal scales. The color, style, and scale of layering show variations with chemical composition, but none of these correlations are consistent between samples. However, there are strong intersample correlations between chemical and S-Fe-Zn isotope compositions at the millimeter scale. Sphalerite precipitated from deep, hydiothermal fluids with S-34-enriched sulfide is enriched in Cd, Sb, Cu, and Ag, whereas Fe and As are enriched in sphalerite precipitated from shallow, bacteriogenic brines with isotopically light S. Significant chemical variations also occur at the micrometer scale in sphalerite regardless of its genetic affinity. These variations are interpreted as being due to variations in temperature, pH, and sulfur activity following the arrival at the site of deposition of pulses of hydrothermal fluids at specific stages of sphalerite growth. Therefore the chemistry of sphalerite, coupled with its texture, appears to be a powerful tool to elucidate fluid typing and ore genesis. The results support the hypothesis that layered sphalerite forms by rapid crystallization due to mixing of two fluids of contrasting physicochemical properties, a process required for the formation of Irish-type and some other hydrothermal deposits including, most notably, Mississippi Valley-type (MVT) deposits. The existence of layered sphalerite, coupled with its texture and chemical composition, may therefore provide useful insight for the mineral exploration industry in Ireland and elsewhere
Going Beyond Counting First Authors in Author Co-citation Analysis
Get PDFThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Diatremes act as fluid conduits for Zn-Pb mineralization in the SW Irish ore field
Get PDFIrish-type mineralization is commonly attributed to fault-controlled mixing of a seawater-derived, sulfur-rich fluid and basement-derived, metal-rich fluid. However, maar-diatreme volcanoes discovered in close spatial and temporal association with Zn-Pb mineralization at Stonepark in the Limerick basin (southwest Ireland) bring a new dimension to established geologic models and may increase the deposit-scale prospectivity in one of the world’s greatest Zn-Pb districts. Stonepark exhibits many incidences of dolomitic black matrix breccias with associated Zn-Pb mineralization, the latter typically occurring within 150 m of the diatremes. Highly negative δ34S pyrite values within country rock-dominated black matrix breccias (–12 to –34) are consistent with sulfide precipitation from bacteriogenic sulfur reduction in seawater-derived brines. However, δ34S values of Zn-Pb sulfides replacing black matrix breccias (–10 to 1) reflect multiple sulfur sources. Diatreme emplacement both greatly enhanced country rock fracture permeability and produced conduits that are filled with porous volcaniclastic material and extend down to basement rock types. Our δ34S data suggest that diatremes provide more efficient fluid pathways for basement-derived fluids. The diatremes introduce another potential sulfur source and facilitate a greater input of metal-rich basement-derived hydrothermal fluid into the system compared to other Irish-type deposits such as Navan and Lisheen, evidenced by Stonepark’s more positive modal δ34S value of –4. Irish-type deposits are traditionally thought to form in association with extensional basement faults and are considered unrelated to extensive Carboniferous magmatism. Our results indicate that a direct link exists between diatreme volcanism and Zn-Pb mineralization at Limerick, prompting a reevaluation of the traditional Irish-type ore formation model, in regions where mineralization is spatially associated with volcanic pipes.</p
Variations on the Author
Get PDF“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
Appropriate Similarity Measures for Author Cocitation Analysis
Get PDFWe provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
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