The beach placer iron deposit of Portman Bay,Murcia, SE Spain: the result of 33 years of tailings disposal (1957–1990) to the Mediterranean seaside

Between 1957 and 1990, the Peñarroya Mining and Metallurgical Company (SMMPE) disposed about 60 million tonnes of tailings materials directly to the Mediterranean Sea. A substantial part of it (12.5 Mt) was dragged back by the sea currents progressively infilling the Portman Bay (Murcia, SE Spain), thus making the shoreline advance between 500 and 600 m seaward. The Roberto froth flotation plant processed mineral from manto-type deposits belonging to the Sierra de Cartagena-La Unión lead-zinc district. One of the mineral assemblages present in these deposits comprises greenalite, magnetite, sulfides, carbonates, and silica. Despite that magnetite recovery was undertaken by SMMPE between 1959 and 1967, we estimate that magnetite contained in the tailings hosts a substantial resource that could be as large as 2.3 Mt of iron ore. The ore contains magnetite ± hematite ± siderite. Tidal waves and sea currents led to gravimetric classification of the tailings material, with concentration of the dense iron oxides in the sandy fractions, eventually forming a coastal placer iron deposit. A major problem for magnetic separation is the intimate intergrowth between magnetite, hematite, and siderite. Besides, the sands contain large concentrations of Pb (0.27 %), Zn (0.72 %), and As (559 ppm).     

Shallow-landslide susceptibility in the Costa Viola mountain ridge (southern Calabria,Italy) with considerations on the role of causal factors

The “Costa Viola” mountain ridge (southern Calabria), in the sector between Bagnara Calabra and Scilla, is particularly exposed to geo-hydrological risk conditions. The study area has repeatedly been affected by slope instability events in the last decades, mainly related to debris slides, rock falls and debris flows. These types of slope movements are among the most destructive and dangerous for people and infrastructures, and are characterized by abrupt onset and extremely rapid movements. Susceptibility evaluations to shallow landslides have been performed by only focusing on source activation. A logistic regression approach has been applied to estimating the presence/absence of sources in terms of probability, on the basis of linear statistical relationships with a set of territorial variables. An inventory map of 181 sources, obtained from interpretation of air photographs taken in 1954–1955, has been used as training set, and another map of 81 sources, extracted from 1990 to 1991 photographs, has been adopted for validation purposes. An initial set of 12 territorial variables (i.e. lithology, land use, soil sand percentage, elevation, slope angle, aspect, across-slope and down-slope curvatures, topographic wetness index, distance to road, distance to fault and index of daily rainfall) has been considered. The adopted regression procedure consists of the following steps: (1) parameterization of the independent variables, (2) sampling, (3) calibration, (4) application and (5) evaluation of the forecasting capability. The “best set” of variables could be identified by iteratively excluding one variable at a time, and comparing the ROC results. Through a sensitivity analysis, the role of the considered factors in predisposing shallow slope failures in the study area has been evaluated. The results obtained for the Costa Viola mountain ridge can be considered acceptable, as 98.1 % of the cells are correctly classified. According to the susceptibility map, the village of Scilla and its surroundings fall in the highest susceptibility class.     

Small-scale landfills: impacts on groundwater and soil

In Brazil, the large quantities of solid waste produced are out of step with public policies, technological developments, and government budgets for the division. In small municipalities, the common lack of technological knowledge and financial conditions for suitable waste disposal has resulted in a large number of illegal dumps. Therefore, small sanitary landfill facilities are working with simplified operations focusing on cost reduction and meeting the economic and technological standards of the city without endangering the environment or public health. Currently, this activity is regulated at a federal level although there is some uncertainty regarding the risk of soil and aquifer contamination as theses facilities do not employ liners. Thus, this work evaluates a small landfill to identify changes in soil and groundwater using geotechnical parameters, monitoring wells, and geophysical tests performed by electrical profiling. It is verified that based on current conditions, no contaminants have migrated via underground water aquifers, and overall no significant changes have occurred in the soil. It is concluded that, despite its simplicity, the method investigated is a viable alternative for the final disposal of municipal solid waste from small cities, especially in developing countries.     

The MED-SUV virtual research environment for enabling the GEO Geohazard supersites in Italy

This paper presents the Virtual Research Environment (VRE) enabling two European GEO Geohazard Supersites in Italy. According to GEO (Group on Earth Observation) vision, Geohazard Supersites provide access to spaceborne and in-situ geophysical data and models for selected sites prone to natural hazards –noticeably, earthquakes and volcano eruptions. The VRE was implemented in the framework of the Mediterranean Supersite Volcanoes (MED-SUV) project, funded by the European Commission. MED-SUV realized one of the European supersite demonstrators covering the two Permanent Supersites selected in Italy: Mt. Etna and Campi Flegrei/Vesuvius. The MED-SUV VRE provides advanced services for heterogeneous data and information management and sharing. MED-SUV started identifying the main supersite requirements including: the interoperability with existing data/information supply systems, the support of policy-based access control, the access to processing capabilities provided by external platforms, the management resources for publishing and sharing new products, the integration with significant global systems such as GEOSS and EPOS. MED-SUV adopted a System of Systems (SoS) approach to address interoperability with the identified heterogeneous systems supplying data and information. The SoS approach is based on a brokering architecture, where a specialized component (i.e the MED-SUV Broker: MSB) connects the existing and next-coming data sources leaving them autonomous. MSB carries out all the necessary mediation and harmonization tasks exposing standard interfaces enabling the interconnection with external systems like GEOSS and EPOS. In addition, MSB is accessible via a JavaScript library implementing Web APIs to facilitate the development of Web and mobile applications.     

Uranium(6+) sorption on montmorillonite: Experimental and surface complexation modeling study

Sorption interactions with montmorillonite and other clay minerals in soils, sediments, and rocks are potentially important mechanisms for attenuating the mobility of U(6+) and other radionuclides through the subsurface environment. Batch experiments were conducted (in equilibrium with atmospheric % MathType!MTEF!2!1!+-% feaafeart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXafv3ySLgzGmvETj2BSbqefm0B1jxALjhiov2D% aebbfv3ySLgzGueE0jxyaibaiiYdd9qrFfea0dXdf9vqai-hEir8Ve% ea0de9qq-hbrpepeea0db9q8as0-LqLs-Jirpepeea0-as0Fb9pgea% 0lrP0xe9Fve9Fve9qapdbaqaaeGacaGaaiaabeqaamaabaabcaGcba% acbiGaiWiG-bfadaWgaaWcbaacbaGaa43qaiaa+9eadaWgaaqaaiaa% +jdaaWqabaaaleqaaaaa!400D!\[P_{CO_2 } \])to determine the effects of varying pH (2 to 9), solid-mass to solution-volume ratio (M/V = 0.028 to 3.2 g/L), and solution concentration (2 × 10^?7 and 2 × 10^?6 M ²³³U) on U(6+) sorption on SAz-1 montmorillonite. The study focused on U(6+) surface complexation on hydroxylated edge sites as the sorption mechanism of interest because it is expected to be the predominant sorption mechanism at pHs typical of natural waters (pH ≈6 to ≈9). Thus, the experiments were conducted with a 0.1 M NaNO₃ matrix to suppress ion-exchange between U(6+) in solution and interlayer cations. The results show that U(6+) sorption on montmorillonite is a strong function of pH, reaching a maximum at near-neutral pH (≈6 to ≈6.5) and decreasing sharply towards more acidic or more alkaline conditions. A comparison of the pH-dependence of U(6+) sorption with that of U(6+) aqueous speciation indicates a close correspondence between U(6+) sorption and the predominance field of U(6+)-hydroxy complexes. At high pH, sorption is inhibited due to formation of aqueous U(6+)-carbonate complexes. At low pH, the low sorption values indicate that the 0.1 M NaNO₃ matrix was effective in suppressing ion-exchange between the uranyl (UO₂ ²⁺) species and interlayer cations in montmorillonite. At pH and carbonate concentrations typical of natural waters, sorption of U(6+) on montmorillonite can vary by four orders of magnitude and can become negligible at high pH. The experimental results were used to develop a thermodynamic model based on a surface complexation approach to permit predictions of U(6+) sorption at differing physicochemical conditions. A Diffuse-Layer model (DLM) assuming aluminol (>AlOH^?) and silanol (>SiOH^?) edge sites and two U(6+) surface complexation reactions per site effectively simulates the complex sorption behavior observed in the U(6+)-H₂O-CO₂-montmorillonite system at an ionic strength of 0.1 M and pH > 3.5. A comparison of model predictions with data from this study and from published literature shows good agreement and suggests that surface complexation models based on parameters derived from a limited set of data could be useful in extrapolating radionuclide sorption over a range of geochemical conditions. Such an approach could be used to support transport modeling by providing a better alternative to the use of constant K _d s in transport calculations.     

Iron release in aqueous environment by fresh volcanic ash from Mount Etna (Italy) and Popocatépetl (Mexico) volcanoes

In this study, we performed leaching experiments for timescales of hours-to-months in deionized water on fresh volcanic ash from Mt. Etna (Italy) and Popocatépetl (Mexico) volcanos to monitor Fe release as a function of ash mineral chemistry and size, with the aim of clarifying Fe release mechanisms and eventually evaluating the impact of volcanic ash on marine and lacustrine environments. To define sample mineralogy and Fe speciation, inclusive characterization was obtained by means of XRF, SEM, XRPD, EELS and Mössbauer spectroscopies. For Etna and Popocatépetl samples, glass proportions were quantified at 73 and 40%, Fe₂O₃ total contents at 11.6–13.2 and 5.8 wt%, and Fe³⁺/Fe_Tot ratios at 0.33 and 0.23, respectively. Leaching experiments showed that significant amounts of iron, ~?30 to 150 and ~?750 nmol g^?1 l^?1 for pristine Etna and Popocatépetl samples, respectively, are released within the first 30 min as a function of decreasing particle size (from 1 to 0.125 mm). The Popocatépetl sample showed a very sustained Fe release (up to 10 times Etna samples) all along the first week, with lowest values never below 400 nmol g^?1 l^?1 and a maximum of 1672 nmol g^?1 l^?1 recorded after 5 days. This sample, being composed of very small particles (average particle size 0.125 mm) with large surface area, likely accumulated large quantities of Fe-bearing sublimates that quickly dissolved during leaching tests, determining high Fe release and local pH decrease (that contributed to release more Fe from the glass) at short timescale (hours-to-days). The fractional Fe solubility (Fe_S) was 0.004–0.011 and 0.23% for Etna and Popocatépetl samples, respectively, but no correlation was found between Fe released in solution and either ash Fe content, glass/mineral ratio or mineral assemblage. Results obtained suggest that volcanic ash chemistry, mineralogy and particle size assume a relevant role on Fe release mostly in the medium-to-long timescale, while Fe release in the short timescale is dominated by dissolution of surface sublimates (formed by physicochemical processes occurring within the eruption plume and volcanic cloud) and the effects of such a dissolution on the local pH conditions. For all samples, a moderate to sustained Fe release occurred for leaching times comparable with their residence time within the euphotic zone of marine and lacustrine environments (variable from few minutes to few hours), revealing their possible contribution to increase Fe bioavailability.     

Continental evaporites and the search for evidence of life on Mars

Continental evaporites are deposits that originate from the evaporation of saline waters in the low areas of saline lakes from all continents, except Europe, and mainly consist of chloride, sulphate and potash minerals. In recent years, the discovery on the Martian surface of hydrated salt minerals, including sulphates and chlorides, interpreted as deriving from the desiccation of preexisting large bodies of water, such as lakes, has provided further convincing evidence of liquid water activity on the surface of Mars and, consequently, it has reinforced the plausibility of finding life. Because evaporites require short‐term aqueous processes for their formation, they can trap and preserve over geologic times a biological record made up of halophilic extremophiles—such as microalgae, bacteria, and their remains—that recent research on Earth has shown to be characterized by unexpectedly high biodiversity. This record may consist of varying types of fossils, including morphological fossils, chemofossils and biominerals. As a consequence, continental evaporite environments and their saline deposits are now a primary target for the near future astrobiology missions devoted to the search for fossil Martian life. Lacustrine evaporite deposits and minerals have, therefore, been identified as primary targets for the NASA–ESA joint programme of the Mars sample return, planned for the end of the current decade. Copyright © 2011 John Wiley & Sons, Ltd.