Geochemical Evidence for Slab Melting in the Trans-Mexican Volcanic Belt

Geochemical studies of Plio-Quaternary volcanic rocks from theValle de Bravo–Zitácuaro volcanic field (VBZ) incentral Mexico indicate that slab melting plays a key role inthe petrogenesis of the Trans-Mexican Volcanic Belt. Rocks fromthe VBZ are typical arc-related high-Mg andesites, but two differentrock suites with distinct trace element patterns and isotopiccompositions erupted concurrently in the area, with a traceelement character that is also distinct from that of other Mexicanvolcanoes. The geochemical differences between the VBZ suitescannot be explained by simple crystal fractionation and/or crustalassimilation of a common primitive magma, but can be reconciledby the participation of different proportions of melts derivedfrom the subducted basalt and sediments interacting with themantle wedge. Sr/Y and Sr/Pb ratios of the VBZ rocks correlateinversely with Pb and Sr isotopic compositions, indicating thatthe Sr and Pb budgets are strongly controlled by melt additionsfrom the subducted slab. In contrast, an inverse correlationbetween Pb(Th)/Nd and ¹⁴³Nd/¹⁴⁴Nd ratios, which extend to lowerisotopic values than those for Pacific mid-ocean ridge basalts,indicates the participation of an enriched mantle wedge thatis similar to the source of Mexican intraplate basalts. In addition,a systematic decrease in middle and heavy rare earth concentrationsand Nb/Ta ratios with increasing SiO₂ contents in the VBZ rocksis best explained if these elements are mobilized to some extentin the subduction flux, and suggests that slab partial fusionoccurred under garnet amphibolite-facies conditions. KEY WORDS: arcs; mantle; Mexico; sediment melting; slab melting     

Chemical and structural study of 1M- and 2M 1-phlogopites coexisting in the same Kasenyi kamafugitic rock (SW Uganda)

In the present work, crystal chemical variations between 1M and 2M ₁ phlogopites coexisting in the same rock sample from kamafugite of Kasenyi (southwest Uganda, west branch of the East African Rift) were explored by electron probe microanalyses, single crystal X-ray diffraction and M?ssbauer spectroscopy. Chemical analyses revealed close similarity both within and between the two polytypic arrangements as well as high TiO₂ (~4.9?wt%) and Al₂O₃ (~12.9?wt%), and low Cr₂O₃ (~0.8?wt%), F (~0.3?wt%) and BaO (~0.2?wt%) contents. Room temperature ⁵⁷Fe M?ssbauer investigation proved that the studied mica is a tetraferriphlogopite with: ^IVFe³⁺?=?19(1)?%, ^VIFe²⁺?=?58(1)?%, ^VIFe³⁺?=?23(1)?%. Single crystal refinement showed that both polytypes have narrow range of variation in terms of some relevant unit cell parameters and similar values in terms of mean bond lengths, mean atomic numbers and distortion parameters. Similar substitutions were active in the structure of the 1M and 2M ₁ studied phlogopites. However, in 2M ₁ polytypes the oxy-type substitutions were found to occur to a greater extent. Comparison of unit layer of 1M mica (in the 2M ₁ setting) with that of the 2M ₁ ones showed that the 2M ₁ polytypes are affected to different extent by relative shifts of the upper and lower triads of octahedral oxygens along the ±b directions. This effect did not cause any symmetry lowering in the T-O-T layer of the studied samples.     

The age and source of late Hercynian magmatism in the central Alps: evidence from precise U−Pb ages and initial Hf isotopes

This study presents U–Pb ages for zircon, titanite, allanite and epidote, and initial Hf isotopic compositions for zircon of Upper Carboniferous granites, diorites and syenites from the Aar massif, central Alps. The rocks were emplaced during three magmatic pulses after Hercynian collisional tectonics: (A) a shoshonitic-ultrapotassic series at 334±2.5 Ma; (B) scattered diorites and granites at 308–310 Ma; and (C) a high-K cale-alkaline granite batholith at 298±2 Ma. Inheritance of old zircons is negligible among all three groups. The Southern Aar granite, in contrast, is a syn-tectonic, probably ca. 350 Ma old granite that contains large amounts of inherited Precambrian zircons. Alpine metamorphism caused weak lead loss in many analyzed zircon fractions, but left the titanite U–Pb system undisturbed: thorites were almost completely reset by Alpine and recent lead loss. Mineral isochrons defined by titanite, allanite, epidote and apatite yield initial Pb isotopic compositions that are in agreement with the model values of Stacey and Kramers. Initial Hf isotopic compositions range from _Hf=–8 to +3.5. The data follow a trend of increasing _Hf with decreasing age. The _Hf versus element concentration relationships suggest mixing between a mantle and a crustal component. These relationships can be explained in terms of generation of the melts from a subcontinental mantle that had been enriched during subduction events at about 1 Ga and by 300 Ma had developed an isotopic signature distinct from that of MORB-type mantle. Further contamination of the melts occurred during ascent and differentiation in the crust. This late Hercynian magmatism can be related to post-collisional strike-slip tectonics.     

Rutile R632 – A New Natural Reference Material for U‐Pb and Zr Determination

A new natural rutile reference material is presented, suitable for U‐Pb dating and Zr‐in‐rutile thermometry by microbeam methods. U‐Pb dating of rutile R632 using laser ablation ICP‐MS with both magnetic sector field and quadrupole instruments as well as isotope dilution‐thermal ionisation mass spectrometry yielded a concordia age of 496 ± 2 Ma. The high U content (> 300 μg g^?1) enabled measurement of high‐precision U‐Pb ages despite its young age. The sample was found to have a Zr content of 4294 ± 196 μg g^?1, which makes it an excellent complementary reference material for Zr‐in‐rutile thermometry. Individual rutile grains have homogeneous compositions of a number of other trace elements including V, Cr, Fe, Nb, Mo, Sn, Sb, Hf, Ta and W. This newly characterised material significantly expands the range of available rutile reference materials relevant for age and temperature determinations.     

Plio-pleistocene volcanism in the Andean Cordillera of Central Chile (33∘ – 40∘ S. L.)

Recent field studies in the Andean Cordillera of Central Chile (33–40 S. L.) have shown a widespread distribution around the Chile-Argentina border of pliopleistocene volcanic and pyroclastic flow (5-1 m. y. K/Ar). The older ages are found in Rio Blanco (Santiago) area and the younger in the Cola de Zorro area. They cover horizontal to sub-horizontally, with strong unconformity their meso-cenozoic basement.In the Rio Blanco area the most silicic rocks are dactic and rhyolitic ignimbrites and lava flows. They are similar to the Rhyolitic Formation (Zeil andPichler, 1967) of northern Chile.South of 36 S. L. most of the rocks are calcalkaline basalts and andesites except for the samples from the Pino Hachado area, which plot nearRittman's alkaline field. Chemical inhomogenety of the plio-pleistocene volcanic rocks is thus present in the Andes of Central Chile.

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Zusammenfassung Neue Arbeiten über die Geologie der Cordillera de los Andes im zentralen Abschnitt Chiles (33–40 S) haben eine enorme Verbreitung von plio/pleistozänen Vulkaniten (5-1 m. a.) vor allem in der Grenzregion mit Argentinien ergeben. Die höheren Alter fand man im Gebiet von Rio Blanco (Santiago) und die jüngsten im Gebiet von Cola de Zorro.Die Vulkanite bedecken mit einer horizontalen bis subhorizontalen Verbreitung und mit einer scharfen Diskordanz alle Gesteinsserien des Mesozoikums und Känozoikums.Im Gebiet von Rio Blanco handelt es sich um Ignimbrite rhyolitischer und dacitischer Zusammensetzung. Die kieselsäurereichsten Proben sind ähnlich den Gesteinen der Rhyolit-Formation vonZeil &Pichler (1967) in Nordchile.Südlich von 36 S hat die Mehrheit der Proben eine andesitische und basaltische Zusammensetzung. Es sind kalkalkaline Gesteine mit Ausnahme der Proben von Pino Hachado, die einen starken alkalinen Trend nach dem Diagramm vonRittmann haben. Auf diese Weise ergibt sich eine chemische Inhomogenität bei den plio/pleistozänen Vulkaniten von Zentralchile.

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Resumen Los más recientes trabajos de geología de campo en la Cordillera de los Andes de Chile Central (33–40 L. S.) han evidenciado enormes extensiones de rocas volcánicas pliopleistocénicas (5-1 m. a.) sobre todo en el área limítrofe con Argentina. Las mayores edades fueron encontradas en el area de Rio Blanco (Santiago) y las más jóvenes en el area de Cola de Zorro.Las rocas volcánicas plio-pleistocénicas cubren con disposición horizontal a subhorizontal y con fuerte discordancia a todas las rocas subyacentes del Meso y Cenozoico.En el area de Río Blanco las rocas son ignimbritas de composición riolítica a dacítica y corresponden a las muestras más silícicas similar a rocas de la Formación Riolítica del norte de Chile deZeil yPichler (1967).Al sur del paralelo 36 S la mayoría de las muestras son de composición andesítica y basáltica de naturaleza calcoalcalina excepto las muestras de Pino Hachado que presentan fuerte afînidad alcalina según el diagrama deRittmann. De esta manera se muestra que existe inhomogeneidad química en las rocas volcánicas plios-pleistocénicas de Chile Central.

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Sources and behavior of arsenic and trace elements in groundwater and surface water in the Poopó Lake Basin,Bolivian Altiplano

Water management in semiarid and arid catchments such as the Poopó Lake Basin requires improved understanding of the complex behavior of the various contaminants, which affect the drinking water quality and considered as crucial for sustainable development of the region. Mechanisms of arsenic (As) release in the surface and groundwater were studied. Hydrochemical data for surface water (4 samples) and groundwater (28 samples) were collected in a small watershed in the Poopó catchment at the highland of the Bolivian Andes (Altiplano). All of them show high electrical conductivity values and moderately oxidizing conditions. The surface water contains high concentration of sulfate and the trace elements As, Zn and Pb in the zone affected by acid mine drainage. There is a large variability of the concentration of As and of the trace elements in the groundwater in the five different regions within the Poopó catchment. The metal concentrations sensitive to changes of redox state and results of speciation modeling suggest that As (V) is a predominant aqueous species, which conforms to the prevailing oxidizing conditions in the shallow groundwater environment. Two generalized trends for As distribution were identified in groundwater: (a) high concentrations are found in the arid zone (100–250 μg/L) in the southern (region III) and in the northwestern (region V) regions, and (b) low concentrations (<50 μg/L) are found in the remaining part of the basin (region I, II and IV). However, the spatial distribution within these regions needs to be investigated further. A conclusion from the present study is that there are multiple sources of As as well as other trace elements (such as Cd, Mn and Zn) in the Poopó Lake Basin. Among the sources and the processes which led to the mobility of As and other trace metals in the region are: (a) weathering of sulfide minerals, (b) oxidation of pyrite and/or arsenopyrite in mineralized areas and (c) desorption from hydrous ferric oxide (HFO) surfaces. In non-mining areas, volcanic ash is suggested to be a significant source of As.     

Supportive elements to the decision-making process in the emergency planning of the Angra dos Reis Nuclear Power Complex,Brazil

Accidents in nuclear power plants are problems of great complexity, mainly due to their consequences, such as the population evacuation from the enterprise influence area. The decision-making and emergency plans must be well articulated and require good local geographic space knowledge and the interactions of their environments. This study is a contribution to the emergency plans for the Almirante Álvaro Alberto Nuclear Power Plant, currently the only nuclear complex in Brazil, located in Angra dos Reis, Rio de Janeiro. The study confirmed the region’s main geoenvironmental aspects as winds and rainfall, landslides and population density were evaluated as important elements in the local emergency process. Their integrated analysis supported scenario identification and critical regional points and highlighted population evacuation escape routes. These important results characterized the support to local emergency management actions and guidelines. Furthermore, the geographic information systems was configured as an integrated spatial and temporal analysis platform to associate meteorological, geological/geomorphological and socio-economic data, playing a key role to support the evacuation planning in the event of nuclear power plant accidents.     

A New Appraisal of Sri Lankan BB Zircon as a Reference Material for LA‐ICP‐MS U‐Pb Geochronology and Lu‐Hf Isotope Tracing

A potential zircon reference material (BB zircon) for laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) U‐Pb geochronology and Hf isotope geochemistry is described. A batch of twenty zircon megacrysts (0.5–1.5 cm³) from Sri Lanka was studied. Within‐grain rare earth element (REE) compositions are largely homogeneous, albeit with some variation seen between fractured and homogeneous domains. Excluding fractured cathodoluminescence bright domains, the variation in U content for all analysed crystals ranged from 227 to 368 μg g^?1 and the average Th/U ratios were between 0.20 and 0.47. The Hf isotope composition (0.56–0.84 g/100 g Hf) is homogeneous within and between the grains – mean ¹⁷⁶Hf/¹⁷⁷Hf of 0.281674 ± 0.000018 (2s). The calculated alpha dose of 0.59 × 10¹⁸ g^?1 for a number of BB grains falls within the trend of previously studied, untreated zircon samples from Sri Lanka. Aliquots of the same crystal (analysed by ID‐TIMS in four different laboratories) gave consistent U‐Pb ages with excellent measurement reproducibility (0.1–0.4% RSD). Interlaboratory assessment (by LA‐ICP‐MS) from individual crystals returned results that are within uncertainty equivalent to the TIMS ages. Finally, we report on within‐ and between‐grain homogeneity of the oxygen isotope systematic of four BB crystals (13.16‰ VSMOW).