Distribution, characterization, and geochemical controls of elements of concern in uranium mine tailings, Key Lake, Saskatchewan, Canada

The distribution of As, Mo, Ni and Se in the aqueous and solid phases of U mine tailings in the Deilmann Tailings Management Facility (DTMF), located at the Key Lake mine in northern Saskatchewan, Canada, was defined using as-discharged tailings samples collected monthly starting in 1996 and core samples collected from the DTMF from 3 locations on 3 occasions between 2004 and 2009. These data indicated that the DTMF can be divided into two geochemical zones; tailings generated from the Deilmann ore body between 1996 and 2000 and tailings from the McArthur River ore body, mined after July 2000. The Deilmann tailings solids are generally characterized by greater elemental concentrations than those in the McArthur River tailings, particularly for As, Co and Ni. These elevated concentrations are attributed to the abundance of Ni–Co–As–S minerals in this ore. The mean aqueous concentrations of As, Mo, Ni, and Se are 3.7, 23.2, 0.14, and 0.02 mg L⁻¹, respectively, in the Deilmann porewaters and 0.20, 4.16, 0.06, and 0.03 mg L⁻¹, respectively, in the McArthur River porewaters. Similarly, the mean As, Mo, Ni, and Se solid phase concentrations are 5.89 × 10³, 69.9, 3.20 × 10³, and 17.4 μg g⁻¹, respectively, for the Deilmann tailings and 440, 13.6, 551, and 3.03 μg g⁻¹ in the McArthur River tailings. Statistically, pH remained unchanged from the time of discharge while Eh values have remained oxic with no significant change between the two tailings types over 15 a of residence time. Results from sequential extractions, thermodynamic modeling, and results of complimentary research indicated that ferrihydrite solubility is the dominant control on aqueous As concentrations and also plays a role in controlling dissolved Mo, Ni and Se.     

Canadian Shield brine from the Con Mine, Yellowknife, NT, Canada: Noble gas evidence for an evaporated Palaeozoic seawater origin mixed with glacial meltwater and Holocene recharge

Dissolved noble gas concentrations were measured in high salinity (270 g/L) Ca(Na)-Cl groundwaters from the Con Mine, Yellowknife, Canada in an effort to discriminate between two possible origins, as either a brine generated by evaporative enrichment in a Paleozoic inland sea, or marine water concentrated by freezing during glacial times. Major ion and isotope geochemistry indicate that brines from the deepest level remain relatively undisturbed by mixing with modern water introduced by mining. Mixing calculations are used to quantify fractions of brine, glacial meltwater and modern water. From this, noble gas concentrations were corrected for excess air with Ne and normalized to 100% brine solution. Over-pressuring of helium and argon in the brine provide age constraints based on the accumulation of geogenic ⁴He and ⁴⁰Ar. Radiogenic age calculations together with the local geological history suggest brine emplacement during early Palaeozoic time, likely during the Devonian when evaporitic inland seas existed in this region. The concentrations of the atmospherically derived noble gases in the brine fraction (Kr = 1.4E-8, Xe = 8.5E-10 cc_STP/cc_H2O) are close to atmospheric equilibrium for brine at 25 °C (Kr = 7.3E-9, Xe = 8.0E-10 cc_STP/cc_H2O), but are far lower than would be expected for closed-system concentration of seawater by freezing (Kr = 2.8E-6, Xe = 4.2E-7 cc_STP/cc_H2O). Thus, despite the complicated mixing history of the brine, the atmospheric and geogenic noble gases provide strong evidence for an origin as air-equilibrated brine from evaporated Paleozoic seawater, which infiltrated via density displacement through existing fractures and faults into the Canadian Shield.     

Sources of radiogenic helium in a clay till aquitard and its use to evaluate the timing of geologic events

Concentrations of dissolved gases (He, Ne, Ar and N₂) were measured in pore waters collected from a Pleistocene (0-80 m depth) and Cretaceous (80-156 m depth) aged, clay-rich, aquitard system using both a conventional copper-tube method and in situ diffusion samplers. Both methods yielded similar results. He data revealed a well-defined increase in concentration with depth, from 1.7 × 10⁻⁸ cm³ He STP g⁻¹ water near the water table (at 2.3 m below ground surface) to 6.9 × 10⁻⁶ cm³ He STP g⁻¹ water at ∼80 m below ground surface (B.G.) The concentration at depth greatly exceeded values for atmospheric solubility at in situ temperatures and could not be attributed to steady-state production from α-decay of U and Th within the aquitard system. Trends in He isotope ratios and concentrations suggest accumulation as a result of both release of residual ⁴He from within the Pleistocene clay-rich till (ca. 87%) and an ascending radiogenic helium flux from underlying Cretaceous-age sediments (ca. 13%). One-dimensional transport modeling of the He data suggests that between 15 ka and 25 ka were required to produce the observed profile. This time frame agrees with studies utilizing isotope tracers (i.e., D/H and ¹⁴C-DIC) to estimate the timing of deposition for the till at this site. Our results demonstrate the utility of using helium, a nonreactive tracer, for delineating hydrogeologic processes in slow permeability geologic strata, and also support the contention that thick clay-rich surficial aquitards can provide long-term containment of contaminants, including hazardous wastes.     

A TEST OF SIGNIFICANCE FOR PARTIAL LEAST SQUARES REGRESSION

Partial least squares (PLS) regression is a commonly used statistical technique for performingmultivariate calibration, especially in situations where there are more variables than samples. Choosingthe number of factors to include in a model is a decision that all users of PLS must make, but iscomplicated by the large number of empirical tests available. In most instances predictive ability is themost desired property of a PLS model and so interest has centred on making this choice based on aninternal validation process. A popular approach is the calculation of a cross-validated r~2 to gauge howmuch variance in the dependent variable can be explained from leave-one-out predictions. Using MonteCarlo simulations for different sizes of data set, the influence of chance effects on the cross-validationprocess is investigated. The results are presented as tables of critical values which are compared againstthe values of cross-validated r~2 obtained from the user's own data set. This gives a formal test forpredictive ability of a PLS model with a given number of dimensions.     

Mapping of seagrass meadows from the lakshadweep islands (India), using aerial photographs

Seagrass meadows from the Lakshadweep islands were mapped with the help of black and white aerial photographs. A maximum of 40 ha seagrass cover was estimated in the lagoon of Minicoy, followed by Kavaratti (34 ha). The total seagrass cover from six major islands of Lakshadweep was estimated to be 112 ha with standing crop of ca 800 metric tonnes. The dominant seagrass species observed wasThalassia hemprichii whileCymodocea rotundata, Halophila ovata, Syringodium isoetifolium andHalodule uninervis were common to these islands.     

胶东石城金矿床成矿流体特征及成矿作用

石城金矿位于胶东牟平-乳山成矿带南端,为多金属硫化物型金矿床。其成矿流体阶段可分为3个,相应的流体包裹体特征为:(1)成矿早期(第1阶段)富CO2包裹体;(2)主成矿期(第2阶段)H2O包裹体和含CO2包裹体;(3)成矿后期(第3阶段)H2O包裹体。第1阶段均一温度为256～360℃,盐度3.71%～6.88%NaCl,第2阶段均一温度为168～270℃,盐度4.49%～10.24%NaCl,第3阶段均一温度为123～178℃,盐度0.35%～7.59%NaCl。其中主成矿期为中低温、低盐度的CO2-H2O-NaCl流体体系。H、O同位素表明石城金矿成矿流体为岩浆水与大气水形成的混合热液,C、O同位素则反映了地幔富CO2流体参与了成矿作用,而S同位素进一步揭示了金矿的成矿物质来源为壳幔相互作用的结果。石城金矿的出现表明研究区至少存在两期成矿事件,早期成矿时代约120Ma,主要为石英+黄铁矿型矿石,晚期成矿时代小于111Ma,主要为多金属硫化物型矿石,以石城金矿为代表。