Constraining groundwater flow,residence times,inter-aquifer mixing,and aquifer properties using environmental isotopes in the southeast Murray Basin,Australia

Environmental isotopes (particularly δ¹⁸O, δ²H, and δ¹³C values, ⁸⁷Sr/⁸⁶Sr ratios, and a¹⁴C) constrain geochemical processes, recharge distribution and rates, and inter-aquifer mixing in the Riverine Province of the southern Murray Basin. Due to methanogenesis and the variable δ¹³C values of matrix calcite, δ¹³C values are highly variable and it is difficult to correct ¹⁴C ages using δ¹³C values alone. In catchments where δ¹³C values, ⁸⁷Sr/⁸⁶Sr ratios, and major ion geochemistry yield similar a¹⁴C corrections, ∼15% of the C is derived from the aquifer matrix in the silicate-dominated aquifers, and this value may be used to correct ages in other catchments. Most groundwater has a¹⁴C above background (∼2 pMC) implying that residence times are <30 ka. Catchments containing saline groundwater generally record older ¹⁴C ages compared to catchments that contain lower salinity groundwater, which is consistent with evapotranspiration being the major hydrogeochemical process. However, some low salinity groundwater in the west of the Riverine Province has residence times of >30 ka probably resulting from episodic recharge during infrequent high rainfall episodes. Mixing between shallower and deeper groundwater results in ¹⁴C ages being poorly correlated with distance from the basin margins in many catchments; however, groundwater flow in palaeovalleys where the deeper Calivil–Renmark Formation is coarser grained and has high hydraulic conductivities is considerably more simple with little inter-aquifer mixing. Despite the range of ages, δ¹⁸O and δ²H values of groundwater in the Riverine Province do not preserve a record of changing climate; this is probably due to the absence of extreme climatic variations, such as glaciations, and the fact that the area is not significantly impacted by monsoonal systems.     

A New Understanding of the Provinces of the Amazon Craton Based on Integration of Field Mapping and U-Pb and Sm-Nd Geochronology

New conventional and sensitive high-resolution ion microprobe zircon U-Pb dating has led to a new understanding of the subdivision and evolution of the Amazon Craton during Precambrian time, with major improvements and changes made to the previous Rb-Sr based model. The interpretation of U-Pb and Sm-Nd isotopic data identifies eight main Precambrian tectonic provinces in the Craton, with ages ranging from 3.1 to 0.99 Ga. Some of the provinces were generated by accretional, arc-related processes (Carajás, Transamazonic, Tapajós-Parima and Rondônia-Juruena) and others by recycling of continental crust (Central Amazon, Rio Negro and Sunsas). The exposed Archean crust is restricted to the east (Carajás and south Amapá in Brazil) and north (Imataca in Venezuela) of the craton, indicating that the Amazon Craton is largely a Proterozoic crust. The Carajás-Imataca (3.10–2.53 Ga) and Transamazonian (2.25–2.00 Ga) Provinces are composed predominantly of granite-greenstone terranes. The Tapajós-Parima (2.10–1.87 Ga) and Rondônia-Juruena (1.75–1.47 Ga) Provinces represent new crust added as orogenic belts, while the Rio Negro (1.86–1.52 Ga) and Sunsas (1.33–0.99 Ga) Provinces originated mainly by magmatic-tectonic recycling of the above two orogenic belts. The only zone with a prominent northeast trend is the poorly known K'Mudku Shear Belt, characterized by a 1.20 Ga shear zone which deforms the rocks of at least three different provinces (Rio Negro, Tapajós-Parima and Transamazonic). The Central Amazon Province comprises mostly Orosirian volcano-plutonic rocks (Uatumã Magmatism) and is a terrane in which the exposed crustal structure and deformation are pluton-related. The Sm-Nd T_DM model ages and _Nd suggest that the Central Amazon Province was generated by the partial melting of Archean continental crust (Carajás Province?), perhaps related to underplating that began at the end of the Tapajós-Parima Orogeny (1.88–1.86 Ga).     

Spectral properties, magnetic fields, and dust transport at lunar swirls

Lunar swirls are albedo anomalies associated with strong crustal magnetic fields. Swirls exhibit distinctive spectral properties at both highland and mare locations that are plausibly explained by fine-grained dust sorting. The sorting may result from two processes that are fairly well established on the Moon, but have not been previously considered together. The first process is the vertical electrostatic lofting of charged fine dust. The second process is the development of electrostatic potentials at magnetic anomalies as solar wind protons penetrate more deeply into the magnetic field than electrons. The electrostatic potential can attract or repel charged fine-grained dust that has been lofted. Since the finest fraction of the lunar soil is bright and contributes significantly to the spectral properties of the lunar regolith, the horizontal accumulation or removal of fine dust can change a surface’s spectral properties. This mechanism can explain some of the spectral properties of swirls, accommodates their association with magnetic fields, and permits aspects of weathering by micrometeoroids and the solar wind.     

On the application of magnetic methods for the characterisation of space weathering products

Space weathering is now commonly accepted to modify the optical and magnetic properties of airless body regoliths throughout the Solar System. Although the precise formation processes are not well understood, the presence of ubiquitous sub-microscopic metallic iron (SMFe) grains in lunar soils and corresponding spectral analyses have explained both the unique optical and magnetic properties of such soils. More recently, a variety of ion irradiation, laser melting and vaporisation and impact experiments have been shown to reproduce these effects in the laboratory. Such experiments are crucial to the study of the formation of SMFe under controlled conditions. To date, more emphasis has been placed on optical analyses of laboratory samples, as these address directly the mineralogical interpretation of remote sensing data. However, the magnetic analyses performed on the Apollo and Luna samples have provided useful qualitative and quantitative evaluation of regolith metallic iron content. These techniques are reviewed here, demonstrated on pulsed laser irradiated olivine powder, and their utility for determining the quantity and size distribution of this metallic iron discussed. Ferromagnetic resonance, multi-frequency magnetic susceptibility, vibrating sample magnetometry and thermomagnetic measurements were carried out. Each showed trends expected for the conversion of paramagnetic Fe²⁺ in olivine to fine-grained Fe⁰, with some grains in the superparamagnetic size range. Although evidence for superparamagnetic iron was found, the quantity of sub-microscopic metallic iron produced in these experiments proved insufficient to make conclusive measurements of either the quantity or size distribution of this iron. Improvements to both the experimental and analytical procedures are discussed to better enable such measurements in the future.     

Characterization of multiple lithologies within the lunar feldspathic regolith breccia meteorite Northeast Africa 001

Abstract– Lunar meteorite Northeast Africa (NEA) 001 is a feldspathic regolith breccia. This study presents the results of electron microprobe and LA‐ICP‐MS analyses of a section of NEA 001. We identify a range of lunar lithologies including feldspathic impact melt, ferroan noritic anorthosite and magnesian feldspathic clasts, and several very‐low titanium (VLT) basalt clasts. The largest of these basalt clasts has a rare earth element (REE) pattern with light‐REE (LREE) depletion and a positive Euanomaly. This clast also exhibits low incompatible trace element (ITE) concentrations (e.g., <0.1 ppm Th, <0.5 ppm Sm), indicating that it has originated from a parent melt that did not assimilate KREEP material. Positive Eu‐anomalies and such low‐ITE concentrations are uncharacteristic of most basalts returned by the Apollo and Luna missions, and basaltic lunar meteorite samples. We suggest that these features are consistent with the VLT clasts crystallizing from a parent melt which was derived from early mantle cumulates that formed prior to the separation of plagioclase in the lunar magma ocean, as has previously been proposed for some other lunar VLT basalts. Feldspathic impact melts within the sample are found to be more mafic than estimations for the composition of the upper feldspathic lunar crust, suggesting that they may have melted and incorporated material from the lower lunar crust (possibly in large basin‐forming events). The generally feldspathic nature of the impact melt clasts, lack of a KREEP component, and the compositions of the basaltic clasts, leads us to suggest that the meteorite has been sourced from the Outer‐Feldspathic Highlands Terrane (FHT‐O), probably on the lunar farside and within about 1000 km of sources of both Low‐Ti and VLT basalts, the latter possibly existing as cryptomaria deposits.     

The origin of shoshonites: new insights from the Tertiary high-potassium intrusions of eastern Tibet

The shoshonitic intrusions of eastern Tibet, which range in age from 33 to 41 Ma and in composition from ultramafic (SiO₂ = 42 %) to felsic (SiO₂ = 74 %), were produced during the collision of India with Eurasia. The mafic and ultramafic members of the suite are characterized by phenocrysts of phlogopite, olivine and clinopyroxene, low SiO₂, high MgO and Mg/Fe ratios, and olivine forsterite contents of Fo₈₇ to Fo₉₃, indicative of equilibrium with mantle olivine and orthopyroxene. Direct melting of the mantle, on the other hand, could not have produced the felsic members. They have a phenocryst assemblage of plagioclase, amphibole and quartz, high SiO₂ and low MgO, with Mg/Fe ratios well below the values expected for a melt in equilibrium with the mantle. Furthermore, the lack of decrease in Cr with increasing SiO₂ and decreasing MgO from ultramafic to felsic rocks precludes the possibility that the felsic members were derived by fractional crystallization from the mafic members. Similarly, magma mixing, crustal contamination and crystal accumulation can be excluded as important processes. Yet all members of the suite share similar incompatible element and radiogenic isotope ratios, which suggests a common origin and source. We propose that melting for all members of the shoshonite suite was initiated in continental crust that was thrust into the upper mantle at various points along the transpressional Red River-Ailao Shan-Batang-Lijiang fault system. The melt formed by high-degree, fluid-absent melting reactions at high-T and high-P and at the expense of biotite and phengite. The melts acquired their high concentrations of incompatible elements as a consequence of the complete dissolution of pre-existing accessory minerals. The melts produced were quartz-saturated and reacted with the overlying mantle to produce garnet and pyroxene during their ascent. The felsic magmas reacted little with the adjacent mantle and preserved the essential features of their original chemistry, including their high SiO₂, low Ni, Cr and MgO contents, and low Mg/Fe ratio, whereas the mafic and ultramafic magmas are the result of extensive reaction with the mantle. Although the mafic magmas preserved the incompatible element and radiogenic isotope ratios of their crustal source, buffering by olivine and orthopyroxene extensively modified their MgO, Ni, Cr, SiO₂ contents and Mg/Fe ratio to values dictated by equilibrium with the mantle.     

Large earthquake‐triggered liquefaction mounds and a carbonate sand volcano in the Mesoproterozoic Wumishan Formation,Beijing, North China

Ten well‐preserved, earthquake‐triggered liquefaction mounds and a carbonate sand volcano have been found in the Mesoproterozoic Wumishan Formation (1550–1400 Ma) in the Beijing area, North China. These features crop out in a roadcut near Zhuanghuwa Village. All ten mounds occur in the same sedimentary layer and have rounded shapes with some concentric and radial fissures arising from the centre. They range from 1.5 to 4 m in diameter and from 10 cm to 30 cm in height. The carbonate sand volcano has a diameter of 110 cm and the ‘crater’ at the top has a depth of about 30 cm. Associated with these mounds and the sand volcano are many ‘normal’ sedimentary structures and numerous soft‐sediment deformation structures. The former include ripple marks, cross‐bedding, stromatolites and desiccation cracks, indicating deposition in a stable shallow‐water peritidal platform environment. The latter include intrastratal faults and folds, seismically formed breccias and carbonate clastic dykes. The morphological features and the genesis of these liquefaction mounds are very similar to mounds formed recently by the great Wenchuan Earthquake of China (2008). Detailed thin‐section study of the mounds found no signs of any kind of biological constructional process; instead it reveals some obvious fluidification and liquefaction characteristics. Comparative studies have shown that these features are probably the products of Mesoproterozoic earthquake activity. Copyright © 2013 John Wiley & Sons, Ltd.     

Geochronological and geochemical constraints on the petrogenesis of alkaline ultramafic dykes from southwest Guizhou Province,SW China

Geochronological, geochemical and whole-rock Sr–Nd isotopic analyses have been completed on a suite of alkaline ultramafic dykes from southwest (SW) Guizhou Province, China with the aim of characterising their petrogenesis. The Baiceng ultramafic dykes have a LA-ICP-MS zircon ²⁰⁶Pb/²³⁸U age of 88.1 ± 1.1 Ma (n = 8), whereas two phlogopites studied by ⁴⁰Ar/³⁹Ar dating methods give emplacement ages of 85.25 ± 0.57 Ma and 87.51 ± 0.45 Ma for ultramafic dykes from Yinhe and Lurong, respectively. In terms of composition, these Late Mesozoic ultramafic dykes belong to the alkaline magma series due to their high K₂O (3.31–5.04 wt.%) contents. The dykes are characterised by enrichment of light rare earth element (LREE) and large-ion lithosphile elements (LILEs) (Rb and Ba), negative anomalies in high field strength elements (HFSEs), such as, Nb, Ta and Ti relative to primitive mantle, low initial ⁸⁷Sr/⁸⁶Sr ratios (0.7060–0.7063) and positive ε_Nd(t) values (0.3–0.4). Such features suggest derivation from low degree (< 1%) partial melting of depleted asthenospheric mantle (garnet-lherzolite), and contamination to various degrees (～ 10%) by interaction with upper crustal materials.     

Groundwater geochemical evolution in the northern portion of the Guarani Aquifer System (Brazil) and its relationship to diagenetic features

The groundwater flow pattern in the northern portion of GAS (Guarani Aquifer System) is characterized by the existence of four regional recharge areas located in São Paulo, Mato Grosso do Sul and Goiás states. From these areas of recharge the regional flow is radial and directed toward the center of the Paraná Sedimentary Basin. Local discharge occurs in portions of outcrop regions. The groundwater has low mineralization and can be classified as Ca or Ca–Mg–HCO₃ type, Na–HCO₃ type and Na–HCO₃/Cl/SO₄ type, this sequence represents the hydrochemical evolution. The mechanisms responsible for this evolution are dissolution of feldspars and removal of the carbonate cement from the sandstone mineral framework, followed by ion exchange, responsible for the increase in the Na concentration and decrease of Ca, and, finally, enrichment in Cl and SO₄ derived from underlying aquifer units. The hydrochemical evolution is consistent with diagenetic features that are observed in the sandstones, with the presence of siliceous cement in the outcrop areas, and carbonate cement toward the center of Paraná Basin.     

The origins and behaviour of carbon in a major semi-arid river,the Murray River,Australia, as constrained by carbon isotopes and hydrochemistry

δ¹³C values of dissolved inorganic C (DIC), dissolved organic C (DOC), and particulate organic C (POC) together with δ¹⁸O and δ²H values of water, δ³⁴S values of dissolved SO₄, and major ion concentrations were measured in the Murray River and its tributaries between November 2005 and April 2007 to constrain the origins and behaviour of riverine C. δ¹³C_DIC values in the Murray River vary between −9.5 and −4.7‰ with a range of <3‰ within any sampling round. δ¹³C_DIC values of the tributaries are −11.0‰ to −5.1‰. DIC concentrations of the Murray River increase from ∼25 mg/L in the middle and upper reaches of the river to 45–55 mg/L in the lower reaches. However, the mass ratio of DIC as a proportion of the total dissolved solids (TDS) decreases from ∼0.6–0.7 in the headwaters to ∼0.2–0.3 in the lower reaches of the river, with similar downstream changes in DIC/Cl ratios. This precludes simple evaporative concentration of DIC and is interpreted as the river evading CO₂; this interpretation is consistent with pCO₂ values that are in the range 550–11,200 ppm volume (ppmv), which are far higher than those in equilibrium with the atmosphere (∼360 ppmv). The δ¹³C_DIC values are similar to those that would be produced by the weathering of marine limestone (δ¹³C ∼ 0‰). However, the lack of marine limestones cropping out in the Murray–Darling Basin and the relatively uniform δ¹³C_DIC values of the Murray River (even in upland reaches where the dominant rock types are metamorphosed silicates and granites) make this unlikely. Rather the high pCO₂ values and δ¹³C_DIC values are best explained by a combination of mineralisation of low δ¹³C organic C and evasion to the atmosphere. The rate of these two processes may attain near steady state and control both DIC concentrations and δ¹³C values.