Mineralogical data on a sulphosalt from the Rhodope mountains,Bulgaria

Zusammenfassung Bei dem Versuch, die Kristallstruktur von Bonchevit zu bestimmen, stellte sich heraus, daß dieses Mineral—bis dahin PbBi₄S₇—aus zwei Phasen besteht. Der Hauptanteil wurde eindeutig als Galenobismutit identifiziert. Der Rest wies nach den Gitterkonstanten (a₀=13,58±0,02 Å, b₀=20,51±0,07 Å, c₀=4,09±0,07 Å) auf ein bisher unbekanntes Mineral hin. Die Raumgruppe ist Bbmm. Ein indiziertes Pulverdiagramm und die dazugehörigen d-Werte werden angegeben.Die Emissionsspektralanalyse zeigt Pb und Bi als Hauptkomponenten, Cu und Ag als Nebenkomponenten und Spuren von Zn und Sn. Die Strukturanalyse führte zu der Formel Me₅S₆, wobei die Me-Atome etwa gleich schwer sind, so daß als chemischo Formel nur Pb₃Bi₂S₆ mit Z=4 in Frage kommt.Strukturell gehört das Mineral in die Gruppe Andorit-Ramdohrit-Fizelyit. Die Verwandtschaft bzw. Identität des Minerals mit anderen Mineralen und synthetischen Verbindungen wird diskutiert.

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Mineralogical data on a sulphosalt from the Rhodope mountains, Bulgaria

Summary During an attempt to determine the crystal structure of bonchevite, this mineral was found to consist of two phases. Previously it was thought to have the composition PbBi₄S₇. The main constituent could unambiguously be identified as galenobismutite. For the rest the lattice constants (a₀=13.58±0,02 Å, b₀=20.51±0,07 Å, c₀=4.09±0.07 Å), indicated a new mineral. Space group is Bbmm. An indexed powder diagram (with d-values) is given.The emission spectrographic analysis shows Pb and Bi to be main components, Cu and Ag to be minor components, and traces only of Zn and Sn. The structure analysis has led to the formula Me₅S₆, with Me-atoms of approximately the same atomic number; therefore, the chemical formula has to be Pb₃Bi₂S₆, with Z=4.In a structural classification the mineral belongs to the andoriteramdohrite-fizelyite-group. The relationships to or the identity with other minerals and synthetic compounds are discussed.

     

The study of metal contamination in urban topsoils of Mexico City using GIS

This research presents and discusses information concerning the spatial distribution of heavy metals (Pb, Cu, Zn, Ba, Co, Cr, Ni and V) in the urban environments of Mexico City using geographical information system and statistical analysis. Superficial soil samples (n = 146) were analyzed. The highest contamination indices were found in the north and center zone of the metropolitan area. In contrast, the surrounding rural fields show a lower impact grade. The higher concentrations of Pb, Cu, Zn and Ba were observed as being related to high vehicular traffic, nevertheless other elements such as Co, Cr, Ni and V do not show anthropogenic influence and their content can be attributed to the parental rock. The results are compared with previous surveys carried out in 2003 in order to evaluate temporal deposition trends. No changes were found on reported concentrations except for Cu and Zn, whose concentration has increased in later years. The results suggest that spatial distribution analysis and results in comparison with previous studies could be useful for the management and sustainable development of the metropolitan area of Mexico City.     

Barium-rich fluids and melts in a subduction environment (La Corea and Sierra del Convento mélanges,eastern Cuba)

Whole-rock compositions of muscovite-bearing amphibolite, trondhjemite, pegmatite and quartz-muscovite rocks from Sierra del Convento and La Corea mélanges (eastern Cuba), as well as mineralogy, record complex circulation of Ba-rich fluids and melts in the subduction environment. Partial melting of fluid-fluxed, MORB-derived amphibolite produced trondhjemite magmas that crystallized at depth, in some cases evolving into pegmatites. Qtz-Ms rocks probably crystallized from primary fluids derived from subducted sediments. All these rocks have elevated concentrations of large-ion lithophile elements, especially Ba (up to 11,810 ppm), presumably released from slab sediments by fluids and/or melts. Fluid–rock interaction produced crystallization of phengite in parental amphibolites. The phengite crystallized in all types of rocks is rich in Ba, with concentric zoning, characterized by Ba-rich cores and Ba-poor rims, indicating a compatible behaviour of Ba in the studied systems. Zoning in phengite is governed primarily by the celadonite (tschermak) exchange vector ((Mg,Fe)Si-(Al)_-2), with more moderate contributions of the celsian (BaAl-(KSi)_-1) and paragonite (NaK_-1) exchange vectors. Late remobilization of Ba at relatively low temperature formed retrograde celsian. The compatible behaviour of Ba in the studied rocks strengthens the importance of the stability of phengite for the transfer of LIL elements from the subduction to the volcanic arc environments.     

Vegetation and environmental conditions in the Doñana Natural Park coastal area (SW Iberia) at the beginning of the last glacial cycle

Detailed reconstructions of the vegetation of Iberia during the last glacial inception are rare due to the limited number of terrestrial sites recording this period. Active retreat of El Asperillo cliff, located on the Atlantic coast of southwestern Iberia, has exposed a fossil organic level dating back to one of the early stades of the last glacial cycle. Pollen and macrofossil analyses from this site show that the Doñana area was covered mainly by steppic vegetation; temperate trees survived the coldest periods, albeit in reduced numbers. Mediterranean taxa are extremely reduced, in contrast with other dry areas of southern Iberia over this time span. This vegetation suggests cold and arid climatic conditions, in accordance with paleoclimatic reconstructions based on several Atlantic marine cores.     

The 2011 submarine volcanic eruption in El Hierro (Canary Islands)

Forty years after the Teneguía Volcano (La Palma, 1971), a submarine eruption took place off the town of La Restinga, south of El Hierro, the smallest and youngest island of the Canarian Archipelago. Precursors allowed an early detection of the event and its approximate location, suggesting it was submarine. Uncertainties derived from insufficient scientific information available to the authorities during the eruption, leading to disproportionate civil protection measures, which had an impact on the island's economy—based primarily on tourism—while residents experienced extra fear and distress.     

In Situ Determination of Au and Cu in Natural Pyrite by Near‐Infrared Femtosecond Laser Ablation‐Inductively Coupled Plasma‐Quadrupole Mass Spectrometry: No Evidence for Matrix Effects

Gold and copper concentrations were determined in natural pyrite by near‐infrared femtosecond LA‐ICP‐QMS, using both sulfide reference materials (pyrrhotite Po‐726 and in‐house natural chalcopyrite Cpy‐RM) and NIST SRM 610 as external calibrators. Firstly, using NIST SRM 610 as the external calibrator, we calculated the Au concentration in Po‐726 and the Cu concentration in Cpy‐RM. The calculated concentration averages for Au and Cu were similar to the values published for Po‐726 and Cpy‐RM, respectively. Secondly, we calculated Au and Cu concentrations taking NIST SRM 610 as an unknown sample and using Po‐726 and Cpy‐RM as external calibrators. Again, the average values obtained closely reflected the preferred concentrations for NIST SRM 610. Finally, we calculated Au and Cu concentrations in natural pyrite using sulfide and silicate reference materials as external calibrators. In both cases, calculated concentrations were very similar, independent of the external calibrator used. The aforementioned data, plus the fact that we obtained very small differences in relative sensitivity values (percentage differences are between 5% and 17% for ⁵⁷Fe, ⁶³Cu and ¹⁹⁷Au) on analyses of silicate and sulfide RMs, indicate that there were no matrix effects related to the differences in material composition. Thus, it is possible to determine Au and Cu in natural sulfides using NIST silicate glasses as an external calibrator.     

Fluid inclusion studies in datolite of low grade metamorphic origin from a Jurassic pillow basalt series in northeastern Hungary

The Jurassic pillow basalt blocks in the Szarvask? Unit in the SW-Bükk Mountains are incorporated into an accretionary mélange of Cretaceous age which had been displaced from the Dinarides to NE-Hungary during the Alpine-Carpathian collision. The pillow basalt series is a part of an incomplete remnant of an ophiolite-like sequence from which ultramafic units and sheeted dikes are almost completely absent. At the studied Egerbakta quarry, closely packed pillow, pillow fragmented hyaloclastite breccia and peperitic facies of submarine basaltic volcanism were recognized. Peperitic facies was formed by local admixture of unconsolidated siliciclastic sediment into the basaltic lava. Basaltic pillows contains short and thin prehnite-chlorite-carbonate-quartz veins formed during the interaction of seawater with the cooling lava, as well as cross-cutting datolite-prehnite-quartzchlorite-albite bearing veins. Calcite in the short cooling cracks crystallised from upheated seawater at around 160°C temperature and 0.5?C0.6 kbar pressure (water depth of about 5?C6 km). Datolite precipitations in veins can be classified into at least three different textural-morphological types but all of them contain methane bearing primary fluid inclusion assemblages, with variable methane/water ratios, suggesting an inhomogeneous entrapment from a heterogeneous aqueous-carbonic fluid. End member primary fluid inclusions contain aqueous liquid with methane rich vapour phase and apparently methane only inclusions characterized by liquid phase on room temperature. A combination of results from fluid inclusion microthermometry, Raman spectroscopy (used not only for phase identification but also for determination of salinities) and temperatures calculated from chlorite compositions, show that the precipitation of datolite had taken place from low salinity (0.2?C2 NaCl equiv. mass%) aqueous-methane fluids under increasing temperature and pressure (from 160 to 210°C, and from 0.6 to 1.1 kbar) conditions. The elevated pressures and temperatures in comparison to the submarine hydrothermal processes suggest that the datolite bearing mineral parageneses had been formed during the progression of Alpine very low grade metamorphic processes.     

Palaeoshoreline for the Late Cretaceous marine platform in the Iberian Trough (Leonese Area, Spain) deduced from outcrop and subsurface analysis

The location of the Late Cretaceous paleoshoreline in the Leonese Area (Iberian Trough, Spain) has been investigated by seismic analysis through isobath and isopach maps. The succession can be divided into two depositional sequences: DS-1 and DS-2. These sequences are composed of fluvial systems at the base, with paleocurrents that flowed eastward and north-eastward. The DS-1 sequence (Late Albian-Middle Turonian) shows intertidal to subtidal and offshore deposits at the top, while the DS-2 sequence (Late Turonian-Campanian) presents intertidal to subtidal, tidal flat and shallow marine and lacustrine deposits at its top. The stratigraphic cyclicity based on systems tracts shows that these two depositional sequences exhibit remarkable eustatic control. Both sequences start at the base with a significant sedimentary supply from fluvial systems, related to eustatic fall episodes, and conclude at the top with transgressive periods. The evolution of the basin reveals the history of base-level changes and associated shifts in depositional trends during successive stages. The deeper sectors of the DS-1 sequence are located towards the northeastern part of the study area while the proximal portion of the basin-margin is located to the southwest. The paleoshoreline is placed in a direction oriented at 120. The variations in thickness are elongated in orientations between 030 and 050 and are mainly related to paleovalleys and tributary fluvial networks that supply sediment through the shoreline. It is possible that these variations may be related to active synsedimentary faults. Depocenters move toward the northeast and east during the DS-2 sequence while the proximal portion of the basin-margin moves to the southwest. The paleoshoreline has an orientation of 155 direction and moves basinward. The isopach maps show a group of corridors oriented at 130?C140 and 165?C170, interpreted as result of accumulation of sandy bodies such as inter and subtidal bars. The fluvial systems are transversal to the paleoshoreline direction.     

Risk of water pollution due to ash–sludge mixtures: column trials

The purpose of this work was to study the risks of water pollution due to the use of mixtures containing wood ash and sewage sludge. Mixtures including sludge and ash may be recycled as fertilizers, and they are economical as they do not integrate commercial limes, but Escherichia coli counts may keep significantly high in such mixtures, because their pH is not alkaline enough. In view of that, it seems interesting to study the E. coli survival in lixiviate from ash?Csludge mixtures including limes rather than from ash?Csludge mixtures alone. Two kinds of experiments were performed using laboratory column trials under saturated flow conditions. The first experiment investigated the chemical leaching behaviour of a mixture of 70% timber-industry wood ashes and 30% urban sewage sludge (% dry weight) at doses equivalent to 10 and 30?Mg/ha. The second experiment studied the survival of E. coli in lixiviates generated from 30?Mg/ha of a mixture consisting in 75% wood ash, 20% sewage sludge and 5% quicklime (% dry weight). In the first experiment, admixture of the ash and sludge achieved a stabilization of elements such as aluminium, iron, magnesium, nickle, carbon monoxide, cadmium, chromium and molybdenum that reduced their solubility compared with that in the ash or sludge alone. Significant solubilisation of heavy metals was not observed, with overall minor risk of chemical water pollution. In the second experiment, although including quicklime E. coli counts were still detected in the lixiviate, indicating risk of water contamination.