Radon emanation of heterogeneous basin deposits in Kathmandu Valley,Nepal

Effective radium-226 concentration (EC_Ra) has been measured in soil samples from seven horizontal and vertical profiles of terrace scarps in the northern part of Kathmandu Valley, Nepal. The samples belong to the Thimi, Gokarna, and Tokha Formations, dated from 50 to 14 ky BP, and represent a diverse fluvio-deltaic sedimentary facies mainly consisting of gravelly to coarse sands, black, orange and brown clays. EC_Ra was measured in the laboratory by radon-222 emanation. The samples (n = 177) are placed in air-tight glass containers, from which, after an accumulation time varying from 3 to 18 days, the concentration of radon-222, radioactive decay product of radium-226 and radioactive gas with a half-life of 3.8 days, is measured using scintillation flasks. The EC_Ra values from the seven different profiles of the terrace deposits vary from 0.4 to 43 Bq kg^?1, with profile averages ranging from 12 ± 1 to 27 ± 2 Bq kg^?1. The values have a remarkable consistency along a particular horizon of sediment layers, clearly demonstrating that these values can be used for long distance correlations of the sediment horizons. Widely separated sediment profiles, representing similar stratigraphic positions, exhibit consistent EC_Ra values in corresponding stratigraphic sediment layers. EC_Ra measurements therefore appear particularly useful for lithologic and stratigraphic discriminations. For comparison, EC_Ra values of soils from different localities having various sources of origin were also obtained: 9.2 ± 0.4 Bq kg^?1 in soils of Syabru–Bensi (Central Nepal), 23 ± 1 Bq kg^?1 in red residual soils of the Bhattar-Trisuli Bazar terrace (North of Kathmandu), 17.1 ± 0.3 Bq kg^?1 in red residual soils of terrace of Kalikasthan (North of Trisuli Bazar) and 10 ± 1 Bq kg^?1 in red residual soils of a site near Nagarkot (East of Kathmandu). The knowledge of EC_Ra values for these various soils is important for modelling radon exhalation at the ground surface, in particular in the vicinity of active faults. Importantly, the study also reveals that, above numerous sediments of Kathmandu Valley, radon concentration in dwellings can potentially exceed the level of 300 Bq m^?3 for residential areas; a fact that should be seriously taken into account by the governmental and non-governmental agencies as well as building authorities.     

Soil formation in Phobjikha Valley,Central Bhutan with special regard to the redistribution of loessic sediments

Soil development and landscape evolution were studied in the basin-shaped Phobjikha Valley at 2900–3200 m a.s.l., to the west of the Black Mountain Range, West Central Bhutan. The local environmental setting with strong along-valley winds, frequent freeze–thaw cycles, extensive dry periods and sparse vegetation cover seems to encourage the generation and short-distance transport of silt-sized particles. The effects of this process are evidenced in the smooth valley morphology and in the nature of the examined pedons. Their involvement in continuing redistribution of local sediments is reflected by a homogeneous silty-clayey and stone-free texture, varying profile depths, buried topsoils and weakly developed recent A horizons. In protected locations, in situ weathering of metamorphic parent materials results in alu-andic features with bulk densities <0.9 g cm^?3, (Al_o + ½Fe_o) > 2%, and phosphate retention >95%. Dominance by Al-hydroxy interlayered clay minerals and large amounts of well-crystallised iron oxides indicate an advanced stage of weathering. In areas of preferred eolian deposition, argic and ferralic features emerge, with clay contents of up to 60% and surface areas of >50 m² g^?1. Under forest, umbric horizons can develop. CEC_eff is below 10 cmol_c kg^?1 at all sites. Cluster and factor analyses of soil chemical and physical parameters confirm the redistribution of local sediments as a dominant factor behind the measured variables. No clear indication of glacial activities in the area was found, whereas the massive silty sediments in the lower parts of most profiles, the presence of debris slopes, and the asymmetric cross sections of the side valleys suggest periglacial conditions. Buried topsoils dated at about 2000 conventional ¹⁴C years BP indicate a weakening or absence of sediment influx under wetter conditions towards the end of the Holocene climate optimum. Charcoal on top of paleosols suggests that human activities of deforestation, grazing and arable agriculture may have contributed to the reactivation of local sediment redistribution until today.     

Characterization of the CO2 fluid adsorption in coal as a function of pressure using neutron scattering techniques (SANS and USANS)

Small angle neutron scattering techniques have been applied to investigate the phase behavior of CO₂ injected into coal and possible changes in the coal pore structure that may result from this injection. Three coals were selected for this study: the Seelyville coal from the Illinois Basin (R_o = 0.53%), Baralaba coal from the Bowen Basin (R_o = 0.67%), and Bulli 4 coal from the Sydney Basin (R_o = 1.42%). The coals were selected from different depths to represent the range of the underground CO₂ conditions (from subcritical to supercritical) which may be realized in the deep subsurface environment. The experiments were conducted in a high pressure cell and CO₂ was injected under a range of pressure conditions, including those corresponding to in-situ hydrostatic subsurface conditions for each coal. Our experiments indicate that the porous matrix of all coals remains essentially unchanged after exposure to CO₂ at pressures up to 200 bar (1 bar = 10⁵ Pa). Each coal responds differently to the CO₂ exposure and this response appears to be different in pores of various sizes within the same coal. For the Seelyville coal at reservoir conditions (16 °C, 50 bar), CO₂ condenses from a gas into liquid, which leads to increased average fluid density in the pores (ρ_pore) with sizes (r) 1 × 10⁵ ≥ r ≥ 1 × 10⁴ Å (ρ_pore ≈ 0.489 g/cm³) as well as in small pores with size between 30 and 300 Å (ρ_pore ≈ 0.671 g/cm³). These values are by a factor of three to four higher than the density of bulk CO₂ (ρ_CO2) under similar thermodynamic conditions (ρ_CO2 ≈ 0.15 g/cm³). At the same time, in the intermediate size pores with r ≈ 1000 Å the average fluid density is similar to the density of bulk fluid, which indicates that adsorption does not occur in these pores. At in situ conditions for the Baralaba coal (35 ^OC, 100 bar), the average fluid density of CO₂ in all pores is lower than that of the bulk fluid (ρ_pore / ρ_CO2 ≈ 0.6). Neutron scattering from the Bulli 4 coal did not show any significant variation with pressure, a phenomenon which we assign to the extremely small amount of porosity of this coal in the pore size range between 35 and 100,000 Å.     

Short-lived radioactive nuclides in meteorites and early solar system processes

Now extinct, short-lived radioactive nuclides, such as ⁷Be (T_1/2 = 53 days), ¹⁰Be (T_1/2 = 1.5 Ma), ²⁶Al (T_1/2 = 0.74 Ma), ³⁶Cl (T_1/2 = 0.3 Ma), ⁴¹Ca (T_1/2 = 0.1 Ma), ⁵³Mn (T_1/2 = 3.7 Ma) and ⁶⁰Fe (T_1/2 = 1.5 Ma), were present in the protosolar nebula when the various components of meteorites formed. The presence of these radioactive isotopes requires a ‘last-minute’ origin, either nucleosynthesis in a massive star dying close in space and time to the nascent solar system or production by local irradiation of part of the protosolar disk by high-energy solar cosmic rays. In this review, we list: (i) the different observations indicating the existence of multiple origins for short-lived radioactive nuclides, namely ⁷Be, ¹⁰Be and ³⁶Cl for irradiation scenario and ⁶⁰Fe for injection scenario; (ii) the constraints that exist on their distribution (homogeneous or heterogeneous) in the accretion disk; (iii) the constraints they brought on the timescales of nebular processes (from Ca–Al-rich inclusions to chondrules) and of the accretion and differentiation of planetesimals.     

Synthesis and characterization of polycrystalline KAlSi3O8 hollandite [liebermannite]: Sound velocities vs. pressure to 13 GPa at room temperature

A polycrystalline specimen of liebermannite [KAlSi₃O₈ hollandite] was synthesized at 14.5 GPa and 1473 K using glass starting material in a uniaxial split-sphere apparatus. The recovered specimen is pure tetragonal hollandite [SG: I4/m] with bulk density of within 98% of the measured X-ray value. The specimen was also characterized by Raman spectroscopy and nuclear magnetic resonance spectroscopy. Sound velocities in this specimen were measured by ultrasonic interferometry to 13 GPa at room T in a uniaxial split-cylinder apparatus using Al₂O₃ as a pressure marker. Finite strain analysis of the ultrasonic data yielded K_S0 = 145(1) GPa, K₀′ = 4.9(2), G₀ = 92.3(3) GPa, G₀′ = 1.6(1) for the bulk and shear moduli and their pressure derivatives, corresponding to V_P0 = 8.4(1) km/s, V_S0 = 4.9(1) km/s for the sound wave velocities at room temperature. These elasticity data are compared to literature values obtained from static compression experiments and theoretical density functional calculations.     

Tracking the fate of dung-derived carbohydrates in a temperate grassland soil using compound-specific stable isotope analysis

Carbohydrates are major organic components of dung and are likely to contribute substantially to increased carbon stocks in manured soils. To investigate this hypothesis, a field-scale experiment was conducted on a temperate grassland site in Devon, UK. C₄ dung (bulk δ¹³C value ?12.6‰) was applied to a temperate grassland C₃ soil (bulk δ¹³C value ?30.3‰) in April and the surface soil beneath cow pats sampled at seven dates over a year. Total carbohydrates were extracted as their monosaccharide components and analysed as the alditol acetates using gas chromatography. The δ¹³C values of the major monosaccharides glucose (?11.5 ±0.6‰), xylose (?10.4 ±0.4‰), arabinose (?10.4 ±0.5‰) and galactose (?8.3 ±1.6‰) extracted from the C₄ dung via acid hydrolysis were indicative of their source. Their weighted mean δ¹³C value was ?10.8‰, 1.8‰ more ¹³C-enriched than the bulk dung value. The δ¹³C values of individual monosaccharides recovered by acid hydrolysis in the 0–1 cm and 1–5 cm soil horizons beneath C₄ cow pats, compared with control soils determined over 372 days, allowed assessment of the extent of incorporation and fluxes of dung-derived monosaccharides. A maximum of 60% of the dung C in soil was derived from carbohydrates after 56 days, declining to around 20% after 372 days. Incorporation dynamics varied between monosaccharide species. Glucose, xylose and arabinose behaved in a similar manner because of their predominantly plant cell wall derived provenance in the dung, whilst dung-derived galactose and mannose appeared to have a microbial source in the soil. The dynamics of total dung-derived monosaccharides in the top 5 cm was comparable to incorporation and flux of bulk dung C, previously estimated using bulk δ¹³C values. The movement of dung-derived carbohydrates into the soil was inequivalent between the 0–1 cm and 1–5 cm horizons. The lack of a significant difference in concentration, but the evidence for the persistence of dung-derived monosaccharides in soil based on δ¹³C values, indicated replacement of existing pools in the soil, suggesting that the ability of this particular soil to sequester further C derived from carbohydrates was limited.     

Effect of organic-matter type and thermal maturity on methane adsorption in shale-gas systems

A series of methane (CH₄) adsorption experiments on bulk organic rich shales and their isolated kerogens were conducted at 35 °C, 50 °C and 65 °C and CH₄ pressure of up to 15 MPa under dry conditions. Samples from the Eocene Green River Formation, Devonian–Mississippian Woodford Shale and Upper Cretaceous Cameo coal were studied to examine how differences in organic matter type affect natural gas adsorption. Vitrinite reflectance values of these samples ranged from 0.56–0.58 %R_o. In addition, thermal maturity effects were determined on three Mississippian Barnett Shale samples with measured vitrinite reflectance values of 0.58, 0.81 and 2.01 %R_o.For all bulk and isolated kerogen samples, the total amount of methane adsorbed was directly proportional to the total organic carbon (TOC) content of the sample and the average maximum amount of gas sorption was 1.36 mmol of methane per gram of TOC. These results indicate that sorption on organic matter plays a critical role in shale-gas storage. Under the experimental conditions, differences in thermal maturity showed no significant effect on the total amount of gas sorbed. Experimental sorption isotherms could be fitted with good accuracy by the Langmuir function by adjusting the Langmuir pressure (P_L) and maximum sorption capacity (Γ_max). The lowest maturity sample (%R_o = 0.56) displayed a Langmuir pressure (P_L) of 5.15 MPa, significantly larger than the 2.33 MPa observed for the highest maturity (%R_o > 2.01) sample at 50 °C.The value of the Langmuir pressure (P_L) changes with kerogen type in the following sequence: type I > type II > type III. The thermodynamic parameters of CH₄ adsorption on organic rich shales were determined based on the experimental CH₄ isotherms. For the adsorption of CH₄ on organic rich shales and their isolated kerogen, the heat of adsorption (q) and the standard entropy (Δs⁰) range from 7.3–28.0 kJ/mol and from −36.2 to −92.2 J/mol/K, respectively.     

Dissolved and particulate zinc and nickel in the Yangtze River (China): Distribution,sources and fluxes

Dissolved and particulate Zn and Ni concentrations were determined at 76 locations along the Yangtze River basin from the headwaters to the estuary during flood and dry seasons. Spatial and temporal variations of Zn and Ni were investigated and six major source zones were identified. The Three Gorges Dam (TGD) blocked most of the suspended loads and extremely low concentration of Zn and Ni were observed downstream of the dam. Dissolved (ranging from 0.062 to 8.0 μg L⁻¹) and particulate (ranging from 12 to 110 mg kg⁻¹) Ni showed similar levels of concentrations during flood and dry seasons, whereas dissolved (ranging from 0.43 to 49 μg L⁻¹) and particulate (ranging from 54 to 1100 mg kg⁻¹) Zn were slightly and much lower in the flood season than dry season, respectively. This was attributed to the increased water discharge during the flood season causing a dilution effect and sediment resuspension. In the flood season, average concentrations of Zn and Ni were higher in the main channel than in tributaries, due to soil erosion and mining activities providing the dominant inputs. The situation was opposite in the dry season, attributed to the contribution of municipal sewage, industrial activities, and waste disposal. During the flood season, dissolved Zn and Ni concentrations were negatively correlated with pH. Water and suspended particulate matter (SPM) from the upper reaches, middle reaches, and lower reaches of the Yangtze River were characterized by their Zn and Ni concentrations. The Panzhihua, Nanling and Tongling mining areas were considered as the most important source zones of particulate Zn and Ni. The Chongqing region, Wuhan region and the Yangtze River Delta provided most of the dissolved Zn and Ni inputs into the river. Annual net flux of Zn (10–72 × 10⁵ kg a⁻¹) and Ni (5.0–19 × 10⁵ kg a⁻¹) in each source zone were estimated according to their respective influent and effluent fluxes. Contributions of the source zones to Zn and Ni transport decreased from the upper reaches to the lower reaches.     

Lithospheric structure of the North China Craton: Integrated gravity,geoid and topography data

The lithospheric structure of ancient cratons provides important constraints on models relating to tectonic evolution and mantle dynamics. Here we present the 3D lithospheric structure of the North China Craton (NCC) from a joint inversion of gravity, geoid and topography data. The NCC records a prolonged history of Archean and Paleoproterozoic accretion of crustal blocks through subduction and collision building the cratonic architecture, which was subsequently differentially destroyed during Mesozoic through extensive magmatism. The thermal structure obtained in our study is considered to define the lithosphere-asthenosphere boundary (LAB) of the NCC, and reflects the density variations within the mantle lithosphere. Employing the Moho depths from deep seismic sounding profiles for the inversion, and based on repeated computations using different parameters, we estimate the Moho depth, LAB depth and average crustal density of the craton. The Moho depth varies from 28 to 50 km and the LAB depth varies from 105 to 205 km. The LAB and Moho show concordant thinning from West to East of the NCC. The average crustal density is 2870 kg m^− 3 in the western part of the NCC, higher than that in the eastern part (2750 kg m^− 3). The results of joint inversion in our study yielded LAB depth and lithospheric thinning features similar to those estimated from thermal and seismic studies, although our results show different depth and variations in the thickness. The lithosphere gently thins from 145 to 105 km in the eastern NCC, where as the thinning is much less pronounced in the western NCC with average depth of about 175 km. The joint inversion results in this study provide another perspective on the lithospheric structure from the density properties and corresponding geophysical responses in an ancient craton.     

Assessing the potential for CO2 adsorption in a subbituminous coal,Huntly Coalfield,New Zealand,using small angle scattering techniques

Small angle scattering techniques (SAXS and SANS) have been used to investigate the microstructural properties of the subbituminous coals (R_max 0.42–0.45%) from the Huntly Coalfield, New Zealand. Samples were collected from the two thick (> 5 m) coal seams in the coalfield and have been analysed for methane and carbon dioxide sorption capacity, petrography, pore size distribution, specific surface area and porosity.Specific surface area (SSA) available for carbon dioxide adsorption, extrapolated to a probe size of 4 Å, ranged from 1.25 × 10⁶ cm^? 1 to 4.26 × 10⁶ cm^? 1 with total porosity varying from 16% to 25%. Porosity was found to be predominantly composed of microporosity, which contributed the majority of the available SSA. Although considerable variation was seen between samples, the results fit well with published rank trends.Gas holding capacity at the reservoir pressure (approximately 4 MPa) ranged from 2.63 to 4.18 m³/t for methane on a dry, ash-free basis (daf) and from 22.00 to 23.72 m³/t daf for carbon dioxide. The resulting ratio of CO₂:CH₄ ranged from 5.7 to 8.6, with an average of 6.7:1.Holding capacities for both methane and carbon dioxide on a dry ash free basis (daf) were found to be correlated with sample microporosity. However, holding capacities for the two gases on an as analysed (aa) basis (that is including mineral matter and moisture), showed no such correlation. Carbon dioxide (aa) does show a negative correlation with both specific surface area and microporosity. As the coals have low inorganic matter content, the reversal is thought to be related to moisture which is likely concentrated in the pore size range 12.5–125 Å. Methane holding capacity, both daf and aa, correlates with macroporosity, thus suggesting that the holding capacity of micropores is diminished by the presence of moisture in the pores.     

Stable isotopic signatures of the modern land snail Eremina desertorum from a low-latitude (hot) dry desert—A study from the Petrified Forest,New Cairo,Egypt

This study was conducted on recent desert samples—including (1) soils, (2) plants, (3) the shell, and (4) organic matter from modern specimens of the land snail Eremina desertorum—which were collected at several altitudes (316–360 m above sea level) from a site in the New Cairo Petrified Forest. The soils and shell_{E. desertorum} were analyzed for carbonate composition and isotopic composition (δ¹⁸O, δ¹³C). The plants and organic matter_{E. desertorum} were analyzed for organic carbon content and δ¹³C. The soil carbonate, consisting of calcite plus minor dolomite, has δ¹⁸O values from −3.19 to −1.78‰ and δ¹³C values −1.79 to −0.27‰; covariance between the two values accords with arid climatic conditions. The local plants include C3 and C4 types, with the latter being dominant. Each type has distinctive bulk organic carbon δ¹³C values: −26.51 to −25.36‰ for C3-type, and −13.74 to −12.43‰ for C4-type plants.The carbonate of the shell_{E. desertorum} is composed of aragonite plus minor calcite, with relatively homogenous isotopic compositions (δ¹⁸O_mean = −0.28 ± 0.22‰; δ¹³C_mean = −4.46 ± 0.58‰). Most of the δ¹⁸O values (based on a model for oxygen isotope fractionation in an aragonite-water system) are consistent with evaporated water signatures. The organic matter_{E. desertorum} varies only slightly in bulk organic carbon δ¹³C values (−21.78 ± 1.20‰) and these values suggest that the snail consumed more of C3-type than C4-type plants. The overall offset in δ¹³C values (−17.32‰) observed between shell_{E. desertorum} carbonate and organic matter_{E. desertorum} exceeds the value expected for vegetation input, and implies that 30% of carbon in the shell_{E. desertorum} carbonate comes from the consumption of limestone material.     

Dissolution kinetics of Devonian carbonates at circum-neutral pH, 50 bar pCO2, 105 °C,and 0.4 M: The importance of complex brine chemistry on reaction rates

The dissolution kinetics of carbonate rocks sampled from the Keg River Formation in Northeast British Columbia were measured at 50 bar pCO₂ and 105 °C, in both natural and synthetic brines of 0.4 M ionic strength. Natural brines yielded reaction rates of −12.16 ± 0.11 mol cm⁻² s⁻¹ for Log R_Ca, and −12.64 ± 0.05 for Log R_Mg. Synthetic brine yielded faster rates of reaction than natural brines. Experiments performed on synthetic brines, spiked with 10 mmol of either Sr or Zn, suggest that enhanced reaction rates observed in synthetic brines are due to a lack of trace ion interaction with mineral surfaces. Results were interpreted within the surface complexation model framework, allowing for the discrimination of reactive surface sites, most importantly the hydration of the >MgOH surface site. Dissolution rates extrapolated from experiments predict that CO₂ injected into the Keg River Formation will dissolve a very minor portion of rock in contact with affected formation waters.     

Toxic metal(loid) speciation during weathering of iron sulfide mine tailings under semi-arid climate

Toxic metalliferous mine-tailings pose a significant health risk to ecosystems and neighboring communities from wind and water dispersion of particulates containing high concentrations of toxic metal(loid)s (e.g., Pb, As, Zn). Tailings are particularly vulnerable to erosion before vegetative cover can be reestablished, i.e., decades or longer in semi-arid environments without intervention. Metal(loid) speciation, linked directly to bioaccessibility and lability, is controlled by mineral weathering and is a key consideration when assessing human and environmental health risks associated with mine sites. At the semi-arid Iron King Mine and Humboldt Smelter Superfund site in central Arizona, the mineral assemblage of the top 2 m of tailings has been previously characterized. A distinct redox gradient was observed in the top 0.5 m of the tailings and the mineral assemblage indicates progressive transformation of ferrous iron sulfides to ferrihydrite and gypsum, which, in turn weather to form schwertmannite and then jarosite accompanied by a progressive decrease in pH (7.3–2.3).Within the geochemical context of this reaction front, we examined enriched toxic metal(loid)s As, Pb, and Zn with surficial concentrations 41.1, 10.7, 39.3 mmol kg⁻¹ (3080, 2200, and 2570 mg kg⁻¹), respectively. The highest bulk concentrations of As and Zn occur at the redox boundary representing a 1.7 and 4.2-fold enrichment relative to surficial concentrations, respectively, indicating the translocation of toxic elements from the gossan zone to either the underlying redox boundary or the surface crust. Metal speciation was also examined as a function of depth using X-ray absorption spectroscopy (XAS). The deepest sample (180 cm) contains sulfides (e.g., pyrite, arsenopyrite, galena, and sphalerite). Samples from the redox transition zone (25–54 cm) contain a mixture of sulfides, carbonates (siderite, ankerite, cerrusite, and smithsonite) and metal(loid)s sorbed to neoformed secondary Fe phases, principally ferrihydrite. In surface samples (0–35 cm), metal(loid)s are found as sorbed species or incorporated into secondary Fe hydroxysulfate phases, such as schwertmannite and jarosites. Metal-bearing efflorescent salts (e.g., ZnSO₄·nH₂O) were detected in the surficial sample. Taken together, these data suggest the bioaccessibility and lability of metal(loid)s are altered by mineral weathering, which results in both the downward migration of metal(loid)s to the redox boundary, as well as the precipitation of metal salts at the surface.     

Cyanobacterial mineralisation of posnjakite (Cu4(SO4)(OH)6·H2O) in Cu-rich acid mine drainage at Yanqul,northern Oman

This is the first detailed account of the copper sulfate posnjakite (Cu₄(SO₄)(OH)₆·H₂O) coating cm-long filaments of a microbial consortium of four cyanobacteria and Herminiimonas arsenicoxydans. It was first observed on immersed plant leaves and stalks in a quarry sump of the abandoned Yanqul gold mine in the northern region of Oman; rock surfaces in the immediate vicinity show no immediate evidence of posnjakite. However, a thin unstructured layer without filaments but also containing the brightly coloured turquoise posnjakite covers ferruginous muds in the sump. Although copper is a potent bactericide, the microbes seem to survive even at the extreme heavy metal concentrations that commonly develop in the sump during the dry season (Cu²⁺ ≈ 2300 ppm; Zn²⁺ = 750 ppm; Fe²⁺ ≈ 120 ppm; Ni²⁺ = 37 ppm; Cr_total = 2.5 ppm; Cl⁻ = 8250 ppm; and SO₄²⁻ = 12,250 ppm; pH ∼2.6), thus leading to the precipitation of posnjakite over a large range of physicochemical conditions. Upon exposure to the prevailing arid climate, dehydration and carbonation quickly replace posnjakite with brochantite (Cu₄(SO₄)(OH)₆) and malachite (Cu₂(CO₃)(OH)₂). To characterise and understand the geochemical conditions in which posnjakite precipitates from undersaturated fluids (according to our thermodynamic modelling of the dominant elements), waters from rainy and dry periods were analysed together with various precipitates and compared with the observed field occurrences. The findings imply that posnjakite should not form in the examined environment through purely inorganic mechanisms and its origin must, therefore, be linked to the encountered microbial activities.     

Resistance of soils to concentrated flow erosion: A review

The soil's resistance to concentrated flow erosion is an important factor for predicting rill and (ephemeral) gully erosion rates. While it is often treated as a calibration parameter in process-based soil erosion models, global change studies require the estimation of erosion resistance from measurable soil properties. Several laboratory and field experiments have been conducted to determine the erosion resistance of various types of soils, but no attempts have been made hitherto to summarize all these data and to explore them for general trends. In this study, all available data on the resistance of topsoils to concentrated flow erosion in terms of channel erodibility (Kc) and critical shear stress (τ_cr) has been collected together with all soil and environmental properties reported in literature to affect the soil erosion resistance. Reported Kc values for cropland topsoils range between 0.002 10^− 3 s m^− 1 and 250 10^− 3 s m^− 1 (n = 470), whereas τ_cr values range between 0 and 15 Pa (n = 522). It is demonstrated that so far, the heterogeneity of measurement methods, the lack of standardized definitions and the shortcomings of the flow shear stress model hamper the comparability of soil erosion resistance values from different datasets. Nevertheless, combining Kc and τ_cr data from different datasets, a general soil erosion resistance ranking for different soil textures can be proposed. The compiled dataset also reveals that tillage practices clearly affect Kc (Kc for conventional tillage > Kc for reduced tillage > Kc for no tillage) but not τ_cr.It was concluded that Kc and τ_cr are not related to each other and that soil and macro-environmental properties affecting the foremost do not necessarily affect the latter as well and vise versa. Often Kc seems to be a more appropriate parameter than τ_cr to represent the differences in soil erosion resistance under various soil and environmental conditions (e.g. bulk density, moisture content, consolidation, tillage). The two parameters represent different quantities and are therefore both needed to characterize the soil's resistance to concentrated flow erosion.     

Evaluation of radiation dose due to naturally occurring radionuclides in rock samples of different origins collected from Azad Kashmir

The state of Azad Kashmir is rich in three types of rocks, namely, sedimentary, metamorphic, and igneous rocks. These rocks contain extensive deposits of graphite, marble, limestone, quartzite, granite, dolerite, and sandstone, which are widely used for the construction of dwellings in Azad Kashmir and Pakistan. Therefore, knowledge about the presence of natural radioactivity in these materials is desirable to assess the radiological hazards associated with it. In this context, 30 rock samples were collected from different geologic formations of the Muzaffarabad Division, Azad Kashmir. After processing the samples, the specific activities of ²²⁶Ra, ²³²Th, and ⁴⁰ K in them were measured using a P-type coaxial high-purity germanium detector. The observed highest dose rate values for sedimentary, metamorphic, and igneous rocks have been found to be 83.16 ± 1.08, 135.87 ± 1.18, and 115.98 ± 1 nGy ⋅ h^–1, respectively. The radium equivalent activity (Ra_eq) varied from 23.76 ± 1.15 for dolerite sample (igneous rock) to 293.69 ± 2.60 Bq ⋅ kg^–1 for marble (metamorphic rock). The Ra_eq values of all rock samples are lower than the limit mentioned in the Organization for Economic Cooperation and Development (OECD, 1979) report (370 Bq ⋅ kg^–1, equivalent to γ-dose of 1.5 mSv ⋅ y^–1). The values of external (H_ex) and internal hazard indices (H_in) are less than unity. The mean outdoor and indoor annual effective dose equivalents are 0.073 mSv ⋅ y^–1 and 0.29 mSv ⋅ y^–1, respectively. The mean (over all types of rock samples) annual effective dose equivalent is reported as 0.36 mSv ⋅ y^–1.     

Mechanisms of continental subduction and exhumation of HP and UHP rocks

We discuss possible scenarios of continental collision, and their relation to mechanisms of exhumation of HP and UHP rocks, inferred from thermo-mechanical numerical models accounting for thermo-rheological complexity of the continental lithosphere. Due to this complexity, mechanisms of continental convergence are versatile and different, in many aspects from those that control oceanic subduction. Elucidating these mechanisms from conventional observations is difficult, and requires additional constraints such as those derived from petrological data. Indeed, exhumation of HP/UHP rocks is an integral part of convergent processes, and burial/exhumation dynamics inferred from metamorphic P–T–t paths provides strong constraints on the collision scenarios. Metamorphic rocks also play an active role due to their contrasting physical properties (rheology, density, fluid transport capacity). Numerical thermo-mechanical experiments suggest that HP/UHP exhumation can only be produced in subduction contexts, as well as that long-lasting (> 10 Myr) continental subduction can only occur in case of cold strong lithospheres (T_Moho < 550 °C, the equivalent elastic thickness T_e > 50 km) and of relatively high convergence rates (> 3–5 cm yr^− 1 ). In this case, high density UHP material in the crustal part of subduction interface provides additional pull on the slab and is not always exhumed to the surface. In case of slower convergence and/or weaker lithosphere (T_e < 40 km), continental subduction is a transient process that takes a limited time span in the evolution of collision zone. Under these conditions, hot mechanically weak UHP rocks enhance decoupling between the upper and lower plate while their exhumation may be rapid (faster than convergence rate) and abundant. Therefore, the UHP exhumation paths can be regarded as sensitive indicators of subduction. Rheological changes and fluid exchanges associated with low-to-middle pressure phase transitions along the subduction interface, such as serpentinization during the oceanic phase and schisting, play a major role producing necessarily mechanical softening of the subduction interface and of the hydrated mantle wedge. The oceanic UHP rocks are exhumed thanks to mixing with low-density continental crustal units during transition from oceanic to continental subduction. At the continental phase, the UHP exhumation occurs as a result of a multi-stage process: at the deep stage (< 40 km depth) the exhumation is rapid and is driven by buoyancy of partly metamorphosed (or partly molten) UHP material often mixed with non-metamorphosed crustal volumes. At final stages, exhumation takes common slow path through the accretion prism mechanism and the erosional denudation. The experiments suggest that formation of UHP rocks requires that continental subduction starts at higher oceanic subduction rate. It then may progressively slow down until the lockup of the subduction interface and/or slab-break-off. A rate of ~ 1–2 cm yr^− 1 is generally sufficient to drive continental subduction during the first several Myr of convergence, but pertinent subduction requires faster convergence rates (> 3–5 cm yr^− 1). We suggest that most continental orogenic belts could have started their formation from continental subduction but this process has been generally limited in time.     

Spatial variability of initial 230Th/232Th in modern Porites from the inshore region of the Great Barrier Reef

The main limiting factor in obtaining precise and accurate uranium-series (U-series) ages of corals that lived during the last few hundred years is the ability to constrain and correct for initial thorium-230 (²³⁰Th₀), which is proportionally much higher in younger samples. This is becoming particularly important in palaeoecological research where accurate chronologies, based on the ²³⁰Th chronometer, are required to pinpoint changes in coral community structure and the timing of mortality events in recent time (e.g. since European settlement of northern Australia in the 1850s). In this study, thermal ionisation mass spectrometry (TIMS) U-series dating of 43 samples of known ages collected from living Porites spp. from the far northern, central and southern inshore regions of the Great Barrier Reef (GBR) was performed to spatially constrain initial ²³⁰Th/²³²Th (²³⁰Th/²³²Th₀) variability. In these living Porites corals, the majority of ²³⁰Th/²³²Th₀ values fell within error of the conservative bulk Earth ²³⁰Th/²³²Th atomic value of 4.3 ± 4.3 × 10^?6 (2σ) generally assumed for ²³⁰Th₀ corrections where the primary source is terrestrially derived. However, the results of this study demonstrate that the accuracy of ²³⁰Th ages can be further improved by using locally determined ²³⁰Th/²³²Th₀ values for correction, supporting the conclusion made by Shen et al. (2008) for the Western Pacific. Despite samples being taken from regions adjacent to contrasting levels of land modification, no significant differences were found in ²³⁰Th/²³²Th₀ between regions exposed to varying levels of sediment during river runoff events. Overall, 39 of the total 43 ²³⁰Th/²³²Th₀ atomic values measured in samples from inshore reefs across the entire region show a normal distribution ranging from 3.5 ± 1.1 to 8.1 ± 1.1 × 10^?6, with a weighted mean of 5.76 ± 0.34 × 10^?6 (2σ, MSWD = 8.1). Considering the scatter of the data, the weighted mean value with a more conservative assigned error of 25% (i.e. 5.8 ± 1.4 × 10^?6) that encompasses the full variation of the 39 ²³⁰Th/²³²Th₀ measurements is recommended as a more appropriate value for initial ²³⁰Th corrections for U-series dating of most Porites samples from inshore regions of the GBR. This will result in significant improvement in both the precision and accuracy of the corrected ²³⁰Th ages related to those based on the assumed bulk Earth ²³⁰Th/²³²Th₀ value of 4.3 ± 4.3 × 10^?6. However, several anomalously high ²³⁰Th/²³²Th₀ values reaching up to 28.0 ± 1.6 × 10^?6 occasionally found in some coral annual bands coinciding with El Niño years imply high ²³⁰Th/²³²Th₀ sources and highlight the complexities of understanding ²³⁰Th/²³²Th₀ variability. For U-series dating of young coral samples from such sites where anomalous ²³⁰Th/²³²Th₀ values occur, we suggest replicate dating of multiple growth bands with known age difference to verify age accuracy.     

Soil evidence for historical human-induced land degradation in West Iceland

Human impacts have been severe on Icelandic soils and vegetation. In order to assess human impact on soils soil quality, soil organic C (SOC), soil bulk density (BD), soil moisture content (SMC), soil mass, and SOC sequestration were measured from two Histosol cores in West Iceland. The cores cover a period from around 665 BC to present, capturing the initial human settlement of Iceland in AD 871. Tephrochronology allowed for a reliable correlation and comparison between the two cores. The initial settlement had profound impacts on the soil quality, causing decreased SOC concentration and SMC, and increased vegetation degradation, soil exposure, eolian deposition, and BD. The total SOC pool was 34.6 kg C m² at one of the sites, of which 60.1% was formed during historic times, driven by increased soil mass deposition from surrounding eroded areas. The SOC pool was 43.7 kg C m² at the other site, of which 31.4% was formed during historic time, constrained by water cycling and decomposition.     

Arsenic associations in sediments from the loess aquifer of La Pampa,Argentina

Groundwater from the Quaternary loess aquifer of La Pampa, central Argentina, has significant problems with high concentrations of As (up to 5300 μg L⁻¹) as well as other potentially toxic trace elements such as F, B, Mo, U, Se and V. Total As concentrations in 45 loess samples collected from the aquifer have a range of 3–18 mg kg⁻¹ with a mean of 8 mg kg⁻¹. These values are comparable to world-average sediment As concentrations. Five samples of rhyolitic ash from the area have As concentrations of 7–12 mg kg⁻¹. Chemical analysis included loess sediments and extracted porewaters from two specially cored boreholes. Results reveal a large range of porewater As concentrations, being generally higher in the horizons with highest sediment As concentrations. The displaced porewaters have As concentrations ranging up to 7500 μg L⁻¹ as well as exceptionally high concentrations of some other oxyanion species, including V up to 12 mg L⁻¹. The highest concentrations are found in a borehole located in a topographic depression, which is a zone of likely groundwater discharge and enhanced residence time. Comparison of sediment and porewater data does not reveal unequivocally the sources of the As, but selective extract data (acid-ammonium oxalate and hydroxylamine hydrochloride) suggest that much of the As (and V) is associated with Fe oxides. Primary oxides such as magnetite and ilmenite may be partial sources but given the weathered nature of many of the sediments, secondary oxide minerals are probably more important. Extract compositions also suggest that Mn oxide may be an As source. The groundwaters of the region are oxidising, with dissolved O₂, NO₃ and SO₄ normally present and As(V) usually the dominant dissolved As species. Under such conditions, the solubility of Fe and Mn oxides is low and As mobilisation is strongly controlled by sorption–desorption reactions. Desorption may be facilitated by the relatively high-pH conditions of the groundwaters in the region (7.0–8.8) and high concentrations of potential competitors (e.g. V, P, HCO₃). PHREEQC modelling suggests that the presence of V at the concentrations observed in the Pampean porewaters can suppress the sorption of As to hydrous Fe(III) oxide (HFO) by up to an order of magnitude. Bicarbonate had a comparatively small competitive effect. Oxalate extract concentrations have been used to provide an upper estimate of the amount of labile As in the sediments. A near-linear correlation between oxalate-extractable and porewater As in one of the cored boreholes investigated has been used to estimate an approximate K_d value for the sediments of 0.94 L kg⁻¹. This low value indicates that the sediments have an unusually low affinity for As.