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The earliest named stromatolite Cryptozoon Hall, 1884 (Late Cambrian, ca. 490 Ma, eastern New York State), was recently re-interpreted as an interlayered microbial mat and non-spiculate (keratosan) sponge deposit. This "classic stromatolite" is prominent in a fundamental debate concerning the significance or even existence of non-spiculate sponges in carbonate rocks from the Neoproterozoic (Tonian) onwards. Cryptozoon has three types of microbially-induced carbonate layers: clotted-pelletoidal micrite with microbial filaments, clotted-pelletoidal micrite with vesicular structure, and dense microcrystalline laminae. A fourth, stratiform to patchy fabric comprises suspect sponges. Using contextual fabric analysis, elemental mapping, cathodoluminescence, fluid inclusions, electron backscatter diffraction, U–Pb dating, and burial history, the sponge interpretation is denied. Neither a distinct sponge body outline nor a canal system is identifiable. Instead, the suspect fabric is secondary in origin, and best explained as a product of Carboniferous (Mississippian) deep burial alteration associated with basement reactivation. Key petrographic observations include heterogenous recrystallization via aggrading Ostwald ripening with interfingering reaction fronts typical for partially miscible fluids, a granoblastic calcite texture (incipient metamorphism), and subsequent hypidioblastic white mica (arguably Carboniferous/Permian, Alleghenian orogeny). Topotype Cryptozoon is a stromatolite altered to sub-greenschist metacarbonate. The published Tonian to Phanerozoic record of interpreted non-spiculate sponges requires reassessment. [ABSTRACT FROM AUTHOR]

The Merguechoum fluorite-barite mineralization, located in the Eastern Meseta of Morocco, is hosted in the Late Hercynian granite. The ore consists of fine crystals of fluorite 1, massive barite 1, euhedral crystals of fluorite 2, and barite 2 with calcite and minor quartz and sulfides. The Merguechoum ore deposits have never been investigated. This study was the first contribution that studied the genesis of fluorite and barite. The ore occurs as dissemination within granite intrusion and also fills the NE-SW-trending meter-sized fractures and faults. The values of the total Rare Earth Elements and Yttrium (REY) and the ratios of LREY/HREY, Y/Ho, Tb/Ca, and Tb/La indicate that the Merguechoum fluorite precipitated from hydrothermal fluids, likely basinal brines, which interacted with the Hercynian granite. The REY data indicate that the ore-forming fluids of the early stage have intensely interacted with the Hercynian granite compared to those of the late ore stage. The gradual decrease in the europium (Eu/Eu*), yttrium (Y/Y*), and cerium (Ce/Ce*) anomalies and a low concentration of ΣREY observed in the second ore stage compared to the first ore stage suggest an increase in pH and fO2 and by inference a decrease in temperature during the evolution of the hydrothermal system. This evolution could be explained by fluid mixing between the ascending basinal hydrothermal fluids and the diluted sulfate-rich meteoric water barite separates from selected samples reveal that the dissolved sulfates (SO42−) were derived from Permian–Triassic sulfates and/or coeval pore-seawater sulfates. The proposed fluid mixing triggered the precipitation of an early-stage F-Ba assemblage followed by the second-stage F-Ba mineralization. Geologic fieldwork, REY inventories, and isotope data point to the ore genesis during the Permian–Triassic extensional tectonic activity concerning the Pangea rifting. This extensional tectonic environment is likely the driving force that mobilized a large amount of the ore-forming basinal brines along the available faults and fractures to the loci of ore deposition. [ABSTRACT FROM AUTHOR]

Petrographic observations and in situ U–Pb ages of melilitites, foidites, basanites, phonolites, and trachytes from the southern part of the Central European Volcanic Province (CEVP) and related plutonic inclusions therein reveal two distinct age groups separated by a gap of ~ 20 Myr. A late Cretaceous to early Eocene group (~ 73–47 Ma; Taunus, Lower Main plain, Odenwald and Kraichgau area, Bonndorfer Graben and Freiburger Bucht area, Vosges and Pfälzerwald) is characterized by nephelinites and basanites mostly devoid of melilite and perovskite, and by rare haüynites, and trachytes. In contrast, a late Oligocene to late Miocene group (~ 27–9 Ma; Lorraine, southern Upper Rhine Graben, Urach, Hegau area) is dominated by melilitites, melilite-bearing nephelinites (both carrying perovskite), and phonolites. Both magmatic episodes are related to domal topographic uplift, erosion, and formation of major angular unconformities in the Upper Rhine Graben, suggesting an association with dynamic topography interrupted by phases of subsidence (or abatements of uplift). The investigated rocks in the southern CEVP (south of a line Eifel–Vogelsberg–Rhön–Heldburg), except for the Kaiserstuhl volcanic complex, mostly comprise small and isolated occurrences or monogenetic volcanic fields, whereas the northern CEVP is dominated by large volcanic complexes and dyke swarms, which are mostly SiO2-saturated to weakly SiO2-undersaturated. In the northern CEVP, evidence of spatially varying but recurrent volcanic activity exists since the Eocene, lacking the distinct 20 Myr gap as documented from the southern CEVP. While the temporal and spatial distribution of volcanism are a result of the Cretaceous to Miocene tectonic evolution in Central Europe, further studies are needed to explain the petrographic differences between the two age groups in the south. [ABSTRACT FROM AUTHOR]

The crush-leach technique is a frequently used method to determine the bulk composition of fluid inclusions trapped in a range of geological samples. We present a modified crush-leach technique combining ion chromatography (IC) and total reflection X-ray fluorescence spectroscopy (TXRF) which allows to determine a range of major, minor and trace elements out of one leachate. To date, trace element detection by means of TXRF is barely used in geosciences, although it combines the advantages of low to very low detection limits (µg/L to ng/L range), small sample amount needed (µL-range) and a fast and inexpensive analytical procedure. Previously described problems of adsorption of polyvalent cations at sample surfaces have been overcome by using acidified water as a leachate. Instead, it has been demonstrated that, for example, the syringe filter type used for IC measurements influences contamination and/or adsorption for a number of elements. The proposed method combination was evaluated for accuracy, reproducibility and system blanks and subsequently applied to quartz samples from hydrothermal vein deposits of the Schwarzwald ore district, SW Germany. [ABSTRACT FROM AUTHOR]

The silver-copper sulfide mineralization associated with the fluorite-barite vein system at the Clara deposit in SW Germany shows large scale vertical zoning. Low to moderate silver contents prevail in the upper 350 m, whereas high silver contents occur in the subsequent 450 m of the currently known vein system. This change in Ag tenor is related to conspicuous mineralogical changes with depth. A detailed petrographic and fluid inclusion study identifies evidence for five subsequent hydrothermal and one alteration stage—all contributing to mineralogical diversity. The vertical Ag zoning, however, is attributed only to the first of these stages. During this first stage, increasing oxidation of ascending hydrothermal fluids (90-160 °C, 24.2-26.7 wt% NaCl+CaCl2) led to the formation of high-Ag tetrahedrite-tennantite in the lower parts and basically Ag-free enargite in the upper parts of the vein system. The subsequent hydrothermal stage led to significant mineralogical changes, but inherited the pre-existing Ag zonation. In this second hydrothermal stage, which was related to fluids similar in composition to those of the first stage (70-125 °C, 23.1-26.5 wt% NaCl+CaCl2), dissolution of high Ag-tetrahedrite-tennantite resulted in the formation of complex Ag-sulfosalts together with moderately Ag-bearing tetrahedrite-tennantite and chalcopyrite. The first two stages were formed by fluid mixing of a sedimentary and a hot basement fluid. The influx of fluids with high Ag, Bi and Pb activity during stage 3 and 5 resulted in the local replacement of earlier Ag-sulfosalts by galena and Ag-(Bi)-sulfosalts. The fourth stage is marked by partial dissolution of sulfides and sulfosalts by a late, hot, undiluted basement fluid (250 °C, 18.7-20.9 wt% NaCl+CaCl2) precipitating fluorite, barite and quartz. Finally, supergene alteration lead to the dissolution of silver-bearing phases and the precipitation of acanthite and native silver. The study illustrates, how metal tenor and mineralogy are decoupled in vertically extensive, polyphase hydrothermal vein systems. This may be pertinent to similarly zoned polymetallic vein systems. [ABSTRACT FROM AUTHOR]