A Cambrian mixed carbonate–siliciclastic platform in SW Gondwana: evidence from the Western Sierras Pampeanas (Argentina) and implications for the early Paleozoic paleogeography of the proto-Andean margin

International Journal of Earth Sciences - The Western Sierras Pampeanas (WSP) of Argentina record a protracted geological history from the Mesoproterozoic assembly of the Rodinia supercontinent to...     

Geochemical signature of provenance in sand-size material in soils and stream sediments near the Tobacco Root batholith, Montana, U.S.A.

Trace-element geochemistry of sandstones are being used to determine provenance. We have conducted preliminary and limited experiments to determine to what extent daughter sands retain the geochemical signature of parent rocks. Six sets of first-order stream sediments, soils from adjacent slopes, and a variety of parent rocks were collected from southwestern Montana, U.S.A. Sampling in a low-relief area ensured that climate and residence time of soils on slopes could be eliminated as variables. Sand-size fractions of stream sediments and soils, and the corresponding parent rocks (granodiorite, quartz monzonite, granite gneiss, biotite-tonalite gneiss and amphibolite) were analyzed for most major elements and selected trace elements. Petrologic modal analysis of the parent rocks and the 0.25–0.50-mm fraction of each sand was done to monitor major mineralogic control, if any, on chemical compositions of the samples.

Our data show that the abundances of the Si and Al in sediments do not discriminate provenance. Abundances of Ca, Mg, Fe and Ti may broadly distinguish between sands derived from metamorphic and igneous source rocks, at least in the area studied. Differences in abundances of the Ba and Th, and the ratio of La/Lu between granitic, tonalitic and amphibolitic parent rocks are preserved in the daughter sediments that we studied. However, the size of the Eu anomaly in the REE patterns of different daughter sediments is not diagnostic of parent rocks. Abundances of Co and Sc distinguish between sediments derived from felsic and mafic rocks. A better provenance discrimination is obtained if the ratios La/Sc, Th/Sc, La/Co, Ba/Sc and Ba/Co are used.

Petrologic modal data show that mineral contents and chemical compositions of parent rocks are compatible with each other. The chemical composition of the sands may be roughly correlated to the petrological modal data but the abundances of some minor and trace elements of sediments cannot be inferred from modal mineralogy. This is expected because these elements may concentrate in accessory minerals and/or may weather out into aqueous or clay mineral fractions; it is also compatible with conclusions of previous studies that some of these elements do not reside in sand-size fractions of siliciclastic sediments.     

The geochemistry of primary and weathered oil shale and coquina across the Julia Creek vanadium deposit (Queensland, Australia)

A significant resource of vanadium and molybdenum exists near Julia Creek, Australia, where the middle Cretaceous organic-rich Toolebuc Formation lies between 0 and 25 m of the surface. We present and discuss a comprehensive geochemical study of the Toolebuc Formation and its enclosing stratigraphy near Julia Creek to understand this ore deposit. V and Mo contents in fresh facies are strongly associated with total organic carbon (TOC) contents, but not with Al or CaCO₃; this suggests that V and Mo were originally concentrated in the organic fraction. However, chemical extractions using H₂O₂ indicate that Mo was originally concentrated in pyrite. The data also suggest that V was mobilised from organic matter during early diagenesis and became associated with clays as little V was extracted by H₂O₂ in the fresh samples. TOC contents in the Toolebuc Formation were removed during weathering, residually enriching trace metals including V and Mo, and as a result, the TOC relationship with V and Mo disintegrates. With weathering, both V and Mo predominantly became associated with iron oxide/hydroxide phases (and possibly other unidentified phases) as these elements in the weathered facies were highly soluble in the sodium citrate–sodium dithionite digestion. Large shale-hosted V and Mo deposits such as Julia Creek offer a potentially viable alternative to the currently mined magnetite-hosted deposits. A thorough understanding of the formation and host mineral phases for V and Mo of these shale deposits, however, is critical to ensure that these valuable metals can be feasibly extracted.     

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Feeding ecology of the northern pipefish,Syngnathus fuscus,in a seagrass community of the lower Chesapeake Bay

Examination of gut contents of the northern pipefish,Syngnathus fuscus, revealed that gammarid amphipods, caprellid amphipods, isopods, and calanoid copepods were the dominant food items during the sevenmonth study period.Gammarus mucronatus, calanoid copepods, andErichsonella attenuata were the seasonally dominant prey items in the spring, summer, and fall, respectively.G. mucronatus and calanoid copepods were consumed in approximate proportion to their numerical abundance in the environment, whileE. attenuata, present in rather uniform densities throughout the study period, was extensively consumed only in the late summer and fall. An ontogenetic pattern of prey consumption was evident, in addition to the seasonal pattern. Comparison ofG. mucronatus andE. attenuata size ranges from the field and in pipefish guts revealed thatS. fuscus preyed upon the smaller size classes of each species, and that mean size of prey consumed was positively related to fish size.     

Late Pan-African magmatism and crustal development in northeastern Egypt

The voluminous Pan-African calc-alkaline granitic suite of the Ras Gharib crustal segment in northeastern Eygpt provides a typical example of orogenic magmatism. The 552 ± 7 Ma-old granodiorite–adamellite and leucogranite suite is compositionally broad (58 to 77 wt.% SiO₂) and exhibits calc-alkaline geochemical trends and trace-element characteristics typical of the volcanic-arc granites. The rocks contain oligoclase, albite, K-feldspar, calcic amphibole, biotite, titanite, zircon, and magnetite. The suite exhibits typical features characteristic of I-type granites. We contend that the magma was formed by partial melting of a modified oceanic crust at an active continental margin during the late stage of the Pan-African orogeny. The process may have involved assimilation of Early Pan-African dioritic country rocks. The more felsic units were produced by progressive fractionation of that magma. The petrological–geochemical evidence suggest that the Pan-African crust in northeastern Egypt did not develop in an extensional tectonic regime, as proposed recently.     

Chemical assembly of Archean anorthosites from amphibolite- and granulite-facies terranes, SW Greenland

We report whole-rock, major- and trace-element compositions (obtained by XRF and INA methods) for the amphibolite-facies Buksefjorden and granulite-facies Nordland anorthosites, SW Greenland. In a previous petrologic study on the same sample suite, we documented differences in texture, mineralogy, and mineral compositions between these two anorthosite bodies. Chemical analyses confirm differences in composition between the two bodies, but these differences cannot be explained by variations in metamorphic conditions, and point towards differences in the nature of their protoliths. Analyzed Nordland samples are anorthosites and leucogabbros with 88-98% normative plagioclase, whereas those from Buksefjorden include anorthosite, leucogabbro, and gabbro with ~55-95% normative plagioclase. Two or more compositional groupings can be recognized at each site, which correspond to differences in color and mineralogy of the hand samples. Samples from Buksefjorden are mainly quartz-normative, whereas those from Nordland are olivine (- nepheline) normative. Other differences include higher Ni/Co ratio and REE contents in the granulite-facies anorthosites from Nordland. REE pattern shapes are similar, however, being moderately fractionated at ~0.5-102 chondrites with positive Eu-anomalies. Calculated equilibrium melt patterns are similar for both anorthosites, being relatively flat at ~50-1502 chondrites, suggesting unfractionated (but evolved) parental magmas. Olivine must have been present in the protoliths of the Nordland rocks compared with Buksefjorden. Otherwise, the protoliths contained plagioclase with variable An-content (~An₆₂-An₉₂) and a mafic component with variable Fe/Mg (mg ~0.3-0.8). This mafic component was either hornblende or a combination of ortho- and clinopyroxene in fixed proportions, plus a small amount of magnetite. Mixing calculations demonstrate that some Buksefjorden anorthosites contain two varieties of plagioclase: a calcic type that may correspond to cumulus crystals, and a sodic-type that may correspond to a trapped-melt component. On plots of normative whole-rock An versus mg, compositions of the Buksefjorden and Nordland anorthosites form crude negative arrays that differ from the generally positive trends of mafic layered intrusions (Kiglapait, Skaergaard) and from the generally flats trends of plagioclase-rich cumulate rocks (St. Urbain and Stillwater anorthosites). This difference provides further evidence for the distinctive nature of Archean calcic-anorthosite complexes compared with other types of mafic intrusions. Moreover, this distribution of data points is consistent with the assembly of the protolith of the SW Greenland anorthosites mainly as mixtures of plagioclase and hornblende. Finally, the field for the Buksefjorden and Nordland anorthosites overlaps only slightly with that for the Fiskenaesset Complex, thus extending the known range of compositions for Archean anorthosites in West Greenland.     

Leaching and differential recrystallization of metamict zircon under experimental hydrothermal conditions

We report results of hydrothermal experiments on four alluvial zircons from Sri Lanka, which cover a wide range of radiation damage, at 450 °C and 1.3 kbar for 744 h with 2 M CaCl₂ solution as reactive fluid. After the hydrothermal treatment, the most metamict samples show micrometer-thick reaction rims, which surround apparently unreacted zircon, as revealed by cathodoluminescence (CL) and Nomarski differential interference contrast (NDIC) images. These rims have sharp, curved, and transgressive boundaries with unreacted zircon and are, in some cases, spread out along cracks. The thickness of reaction rims increases with increasing cumulated !-dosage of the starting materials. The reaction rims are strongly enriched in Ca (up to 7000 ppm) and a water species and depleted in radiogenic Pb, Zr, and Si, as revealed by electron microprobe analyses. A significant Th loss from the reaction rims was detected in the case of the most metamict sample, whereas U remained in the structure. FT-infrared spectrometry and X-ray diffraction measurements revealed that the bulk run products were recrystallized. Using micro-Raman spectrometry, we were able to demonstrate that differential recrystallization took place. The reaction rims are strongly recrystallized, whereas the unreacted grain interiors underwent only minor recrystallization. Recrystallization of the rims is accompanied by an enhancement of the integral CL intensity. It is suggested that recrystallization in the reaction rims was catalyzed by water infiltration and ion exchange and prevented significant congruent zircon dissolution under the given experimental conditions. Previous zircon studies have shown that (1) a transgressive morphology, (2) a reduced Th-U ratio, and (3) an enhanced CL emission are also characteristics of rims in zircons from high-grade metamorphic rocks. Based on these similarities between natural and experimentally produced rims, it is suggested that leaching-catalyzed recrystallization is an important alteration process in zircon under wet geological conditions and can account for many complex core-rim structures found in natural zircons. Furthermore, the strong enrichment of Ca in the reaction rims supports previous assumptions that high Ca concentrations in natural zircons are of secondary origin. It is suggested that lower U-Pb concordia intercept ages obtained from single-phase zircons with high Ca contents date a leaching event.     

Fluorapatite and fluorite solubility controls on geothermal waters in Yellowstone National Park

Potential solubility controls on phosphorus in Yellowstone National Park geothermal waters were investigated using the analytical phosphate estimates of Stauffer and Thompson (1978), the computer program, WATEQF, and adopting the equilibrium constant: $\text{log}\text{K}{}_{\mathrm{25°}}\text{= ?61.4}$ for fluorapatite (FAP = Ca₅(PO₄)₃F) dissolution. The near-boiling high-Cl geyser and spring effluents are at or near saturation with respect to (with) FAP. The sixteen representative springs in this category had FAP saturation indices ($\text{S.I. =}\text{log}\text{IAP/K}{}_{\mathrm{r}}$) ranging from ? 3.2 to +4.9 and averaging +0.9. The strongly positive indices were all associated with the highly alkaline conditions resulting from adiabatic cooling in the near surface environment. Hot spring waters indicating extensive dilution (reduced Cl) by meteoric water have lower pH's, and despite PO₄ and Ca concentrations an order of magnitude higher than the geysers, are still frequently undersaturated with FAP. The travertine-depositing “Mixed-water” springs are invariably supersaturated with FAP at ground surface and at or near saturation with hydroxylapatite. Supersaturation may result from kinetic inhibition of apatite crystallization by the elevated Mg²⁺, HCO₃^?, and lower temperatures in these springs. The phosphates may be residuals of the meteoric dilution water.Separately, if Strübel's temperature-dependent estimates of fluorite (CaF₂) solubility are adopted, the high-Cl geysers and springs on “Geyser Hill” and at Norris are consistently undersaturated with CaF₂ at the 90–100° orifice temperatures. The apparent disequilibrium may reflect fluorite equilibration at the much higher temperatures (> 200°C) in the deeper enthalpy reservoirs.