Comparison between Nickel-Sulfur Fire Assay Te Co-precipitation and Isotope Dilution with High-Pressure Asher Acid Digestion for the Determination of Platinum-Group Elements,Rhenium and Gold

The accurate determination of platinum-group elements (PGE), rhenium and gold is important in both fundamental research and ore deposit studies. Questions have been raised by some authors as to whether the nickel-sulfur fire assay technique (NiS-FA) efficiently collects all the PGE. On the other hand, most isotope dilution (ID) techniques can only treat small test portion masses (2 g was used for high-pressure asher digestion; HPA) and this makes them more vulnerable to nugget effects. We determined PGE concentrations in ten reference materials with the aim of comparing the performance characteristics of the two methods. Both methods determine Ru, Pd, Os, Ir and Pt and we found that there were no significant systematic differences in the recovery. The advantages of NiS-FA were that: (a) it is capable of determining Rh and Au; (b) the relatively large test portion mass (15 g) reduces the nugget effect and (c) it is faster and less expensive than HPA-ID. The advantages of HPA-ID were that: (a) it determined Re and (b) it had low level blanks, lower detection limits and hence better precision in low-level homogeneous samples. Each technique had advantages and limitations; they should be considered as complementary rather than competing techniques.     

Desalination of a sedimentary rock aquifer system invaded by Pleistocene Champlain Sea water and processes controlling groundwater geochemistry

The objective of this study was to identify geochemical processes and Quaternary geological events responsible for the variations in groundwater geochemistry observed in a sedimentary rock aquifer system, including brackish to saline groundwater. Inorganic constituents and environmental isotopes were analyzed for 146 groundwater samples. Dissolution of carbonates dominates in recharge areas, resulting in Ca-, Mg-HCO₃ groundwater. Further along flow paths, under confined conditions, Ca²⁺–Na⁺ ion exchange causes groundwater evolution to Na-HCO₃ type. Na-Cl groundwater is also found and it falls on a seawater mixing line. Using conservative tracers, Cl⁻ and Br⁻, the original Champlain Sea water is shown to have been, in the region, a mixture of about 34% seawater and 66% freshwater, a composition still retained by some groundwater. Na-Cl groundwater thus results from mixing with former Champlain Sea water and also from solute diffusion from overlying marine clay. The system is thus found to be at different stages of desalinization, from the original Champlain Sea water still present in hydraulically stagnant areas of the aquifer to fully flushed conditions in parts, where more flow occurs, especially in recharge zones. The geochemical processes are integrated within the hydrogeological context to produce a conceptual geochemical evolution model for groundwater of the aquifer system.     

Selenium Concentrations in Twenty-Six Geological Reference Materials: New Determinations and Proposed Values

The interest in selenium concentrations in whole rocks is growing, in part because it is a useful tool for base and precious metal exploration. Selenium is often neglected in whole rock geochemistry because of the inability of most laboratories to make reliable determinations of this element. A consequence of these difficulties is a paucity of assigned or certified values for Se in international geological reference materials, so that the "best practice" proposed by Kane and Potts (2007) to obtain robust values for such reference materials cannot be followed. In order to address this problem, we have determined Se by pre-concentration on thiol-cotton fibre followed by INAA (Se/TCF-INAA technique) in twenty-six international geological reference materials, and one quality control material (KPT-1). These values were used, in conjunction with a set of published values, to estimate Se concentrations for these twenty-seven reference samples. Robust statistics were developed for seven of the RMs, with standard deviations equal to or less than precisions calculated using the Horwitz function and so that consensus values could be proposed. For three of the RMs, the presence of outliers gave less robust results, and suggested values are proposed. For seventeen of the RMs, only information values are provided, because either insufficient determinations were available or because large standard deviations of the data were derived.     

RX J1856.5-3754 as a possible strange star candidate

RX J1856.5-3754 has been proposed as a strange star candidate due to its very small apparent radius measured from its X-ray thermal spectrum. However, its optical emission requires a much larger radius and thus most of the stellar surface must be cold and undetectable in X-rays. In the case the star is a neutron star such a surface temperature distribution can be explained by the presence of a strong toroidal field in the crust (Pérez-Azorín et al.: Astron. Astrophys. 451, 1009 (2006); Geppert et al.: Astron. Astrophys. 457, 937 (2006)) We consider a similar scenario for a strange star with a thin baryonic crust to determine if such a magnetic field induced effect is still possible. This work was partially supported by PAPIIT, UNAM, grant IN119306. J.A.H. studies at UNAM and travel to London are covered by fellowships from UNAM’s Dirección General de Estudios de Posgrado.     

Fluid inclusion and carbon, oxygen, and strontium isotope study of the Polaris Mississippi Valley-type Zn–Pb deposit, Canadian Arctic Archipelago: implications for ore genesis

The Polaris deposit is one of the largest Mississippi Valley-type deposits in the world, with 22 million tonnes of ore at 14% Zn and 4% Pb contained in a single, compact orebody surrounded by dolomitized host rocks. Using detailed sampling of carbonates in the orebody and the dolostone halo, this paper aims to characterize the temporal and spatial evolution of the mineralizing system, and to understand the mechanisms that controlled the accumulation of this large, compact Zn–Pb deposit. Five types of dolomite have been distinguished, including three replacement (RD) and two pore-filling dolomites (PD). The paragenetic order is RD1, RD2, RD3, PD1, and PD2. Pore-filling calcite (PC) postdates all other minerals. In most cases, sulfides and dolomite did not co-precipitate, but sphalerite and galena largely overlap with RD3 and PD1. Various dolomites are dissolved or replaced by sulfide-precipitating fluids; sulfides in turn can be overgrown by dolomites. Colloform texture in sphalerite is widespread. Fluid inclusions were studied in RD3, PD1, PD2, sphalerite, and PC. The overall ranges of homogenization temperatures (T _h) and last ice-melting temperatures (T _m-ice) for fluid inclusions in dolomites and sphalerite are from 67 to 141 °C and from −46.7 to −27.0 °C, respectively, consistent with warm basinal brines with high salinities and Ca/Na ratios. Gas chromatographic analysis of these fluid inclusions indicates low concentrations of hydrocarbons (<0.06 mol%). C, O, and Sr isotopes were analyzed for all dolomites and PC, as well as for the fine-grained host limestone and early diagenetic calcite (SC–RC). The isotopic values of RD2, RD3, PD1, and PD2 cluster tightly and form largely overlapping domains. With respect to the host limestone, they are depleted in ¹⁸O, similar in δ¹³C, and slightly enriched in ⁸⁷Sr. There are no regular spatial variations for fluid inclusion and isotope data, indicating an overall geochemical homogeneity in the hydrothermal system. However, certain samples close to the fracture zones in the orebody with slightly elevated T _h and ⁸⁷Sr/⁸⁶Sr values and depleted δ¹⁸O values suggest that the fracture zone was the conduit for the hot brines. Based on the geological and geochemical characteristics of the deposit, we propose that sulfide precipitation at Polaris was caused by mixing of a reduced, metal-rich, sulfur-poor fluid with a reduced, metal-poor, sulfur-rich fluid at the site of mineralization. The metal-carrying fluid ascended along fractures from below the deposit and was hotter than the host rocks, whereas the reduced sulfur-carrying fluid was delivered to the site of mineralization laterally and was in thermal equilibrium with the host rocks. This model can readily explain the dissolution of dolomite during sulfide precipitation and the abundance of colloform sphalerite, as well as the low concentrations of hydrocarbons in fluid inclusions. Accepted: 20 December 1999     

Hydrogeochemistry and groundwater origin of the Basses-Laurentides sedimentary rock aquifer system, St. Lawrence Lowlands, Québec, Canada

A comprehensive hydrogeochemical study was carried out in the Paleozoic Basses-Laurentides sedimentary rock aquifer system in Québec over a 1500 km² study area. Groundwater samples were collected at 153 sites, characterizing all geological and hydrogeological units to a maximum depth of 140 m. Groundwater was analyzed for major, minor and trace inorganic constituents, stable isotopes δ ²H, δ ¹⁸O, and δ ¹³C of dissolved inorganic carbon (DIC), and some samples were analyzed for ³H, and ¹⁴C of DIC. The regional distribution of groundwater types shows that the hydrogeological conditions exert a dominant control on the major ions chemistry of groundwater. Preferential recharge areas are characterized by tritiated Ca-Mg-HCO₃ groundwater, and confined conditions by submodern Na-HCO₃ and Na-Cl groundwater types. Two groundwater end-members are identified in the aquifer system, modern meteoric water and Pleistocene Champlain Sea water. The region displays significant variations of groundwater geochemistry and quality controlled by glaciation, Champlain Sea invasion, lithological rock diversity, and flow system scales. This situation leads to varied groundwater types and origins within a restricted area.     

Quantification of Metals and Semimetals in Carbon‐Rich Rocks: A New Sequential Protocol Including Extraction from Humic Substances

We have developed a new sequential extraction technique that does not require complex procedures and is efficient in determining metal and semimetal contents of carbon‐rich rocks. Six geological reference materials (SBC‐1, SCHS‐1, SCo‐1, SDO‐1, SGR‐1b and SLg‐1) and an in‐house black shale (SH‐1) were selected to test the method, which consists of four main digestion steps involving: (a) dilute HCl acid; (b) NaOH; (c) aqua regia; and (d) hydrofluoric acid. Compared with traditional aqua regia + hydrofluoric acid attack, this new protocol recovers more of the moderately volatile elements during early extraction of humic substances. In addition when compared with reference values, those for most elements are in agreement within uncertainty. Furthermore, this new protocol reveals important information on the partitioning of elements; for instance, steps one and two indicate which elements are associated with carbonates and organic phases from fulvic and humic acid extractions, whereas step three provides results for which elements are associated with sulfide minerals and step four indicates which elements remained in the silicate and oxide phases.     

Talaya batraba gen.et sp.nov.- the First Nymph of a Protopsyllidiid(Hemiptera:Sternorrhyncha:Psyllomorpha) from the Lower Cretaceous Amber of Lebanon

A hemipteran nymph of the sternorrhynchan lineage,placed in the family Protopsyllidiidae is the first found in the fossil record,based on an inclusion in amber from the Lower Cretaceous of Hammana / Mdeyrij,Abeih Formation,Central Lebanon.Based on distinctive features such as a median dorsal elevation and the presence of a large,conical,exposed,setiferous anal tube,the fossil is placed in Talaya batraba gen.et sp.nov.and the newly erected taxon is compared to known nymphs of extinct Protopsyllidiidae.The evolutionary traits of the family and its relatives are considered.     

Narrowing gaps between research and policy development in climate change adaptation work in the water resources and agriculture sectors of Cambodia

Narrowing research and policy, while challenging, is especially important in climate change adaptation work (CCA) due to the high uncertainties involved in planning for climate change. This article aims to seek stakeholders’ opinions regarding how research and policy development can be bridged within the Cambodian water resources and agriculture sectors. The study used institutional ethnography methods with informants from government organizations, local academia, and development partners (DPs). This article identifies a number of challenges, and barriers for narrowing research–policy development gaps, including: limited effectiveness of governmental policies and planning; lack of relevant information required to promote evidence-based planning and policy development; and communication barriers. Evidence-based planning is valued by government officials most when there is actual and effective implementation of policies and plans. In practice, this often implies that governmental policies and plans need be scoped and scaled down to meet the available budget, and thus be achievable. In the long term, it also means building the capacity for policy-relevant research on climate change adaptation within Cambodia. Engaging policy stakeholders in research process for co-producing adaptation knowledge, and introducing knowledge intermediaries are suggested by informants as means to narrowing gaps between research and policy development. The presence of the Cambodia's Prime Minister in research–policy dialogues is recommended as important for attracting the attention of high-level policy makers.

Policy relevance

As a least developed and highly climate-vulnerable country, Cambodia has received climate change funding to implement a number of climate adaptation initiatives. Cambodia is likely to receive more climate change finance in the future. This article aims to assist evidence-based planning, in particular, through policy-relevant research on CCA, so that resources for adaptation in Cambodia are used effectively and efficiently. This research also directly benefits the sustainable development of the country.