Zircon and sphene as fission track geochronometer and geothermometer: A reappraisal

The data published earlier on zircon and sphene fission track ages and annealing are discussed in the light of different etching conditions used for age determination and annealing experiments in order to explain the age discordances of some zircon and sphene pairs, as well as numerous closing temperatures obtained for individual minerals. Using the new set of simple etching conditions, zircon (KOH melt) and sphene (HF+HCl), the annealing experiments indicate that tracks in sphene are annealed more easily than in zircon. The closing temperature of zircon and sphene have been calculated at 300° and 250° C respectively. The study reveals that both the fission track age and the closing temperature of a mineral can vary considerably if different etchants are used. For different etching conditions the closing temperatures (T) of sphene have the following order: ^T NaOH> ^T HF+HCl+HNO₃+H₂O> ^THF+HCl>^THCl. An alternative method can be used to obtain thermal histories of rocks by selectively applying various etchants on the same mineral.     

Modified biomass of Phanerochaete chrysosporium immobilized on luffa sponge for biosorption of hexavalent chromium

Phanerochaete chrysosporium, a white rot basidiomycete, was immobilized over Luffa cylindrica sponge discs, treated with 0.1 N HCl and its potentiality for the removal of hexavalent chromium [Cr(VI)] from water was investigated in both batch and in up-flow fixed-bed bioreactor. The acid treatment of biomass increased the uptake capacity and percentage removal of Cr(VI) from 33.5 to 46.5 mg g^?1 and 67 to 92 %, respectively. Maximum uptake of Cr(VI) was achieved at pH 2, temperature 40 °C after 100 min of contact time. The Cr(VI) sorption on the biomass was better explained by Langmuir isotherm. Thermodynamic studies indicated that the process was spontaneous and endothermic. Sorption kinetic study showed that pseudo-second-order model best correlates the Cr(VI) sorption on the biomass as compare to pseudo-first-order kinetic model. The performance of fixed-bed bioreactor was evaluated at different bed heights (5, 15 and 25 cm) and flow rates (1.66, 4.98 and 8.33 mL min^?1) by using bed depth service time model. Response surface methodology statistical method was applied for optimizing the process parameters. FTIR analysis showed that amino groups were mainly involved in adsorption of Cr(VI).     

Biodegradation of polyvinyl alcohol-low linear density polyethylene-blended plastic film by consortium of marine benthic vibrios

Marine bacteria, Vibrio alginolyticus and Vibrio parahemolyticus isolated from sediments were evaluated for their ability as a consortia, to degrade polyvinyl alcohol-low linear density polyethylene (PVA-LLDPE)-blended plastic films in shake flask conditions at 120 rpm at 37 °C over 15 weeks. Results indicated that relatively 20 % decrease in tensile strength of the film could be achieved with 25 and 30 % blend of PVA in the PVA-LLDPE plastic film compared to other ratios. Micrographs obtained with scanning electron microscope showed visible cracks and grooves on the surface of the PVA-LLDPE blend film after 15 weeks of incubation with bacterial consortium. The decrease in tensile strength of the PVA-blended plastic films after treatment and the results of the scanning electron microscopic analysis evidence that the consortium could cause degradation of PVA-LLDPE plastic blends compared to suitable controls. This is the first report on polyvinyl alcohol degrading Vibrio sp. from marine sediments and its application in microbial degradation of polyvinyl alcohol-low linear density polyethylene plastic blends. The study indicated potential of marine benthic vibrios that have novel enzymes and unique characteristics for application in bioremediation and solid waste management particularly in handling synthetic polymers such as PVA-blended plastic films.     

Geochemistry of Ordovician Keli Group basalts associated with Besshi-type Cu-Zn deposits from the southern Trondheim and Sulitjelma mining districts of Norway

Besshi-type volcanogenic Cu-Zn deposits in the Scandinavian Caledonides are hosted by Ordovician metabasalts and clastic sediments of the Storen, Fundsjo and Sulitjelma groups. The basalts are transitional between T-MORB and marginal basin tholeiites in composition and are characterised by Nd and Pb isotopic compositions which overlap the more radiogenic values of Lower Palaeozoic MORB. These features, along with the intercalation of the basalts with tuffs and continentally derived sediments, indicate an epicontinental rift or marginal basin origin, possibly analogous to the present Red Sea and Gulf of Aden rifts. This implies the development of a restricted ocean basin in the north of Iapetus between the Laurentian and Baltoscandian microcontinents during the Cambrian and Early Ordovician.     

Distribution and speciation of phosphorus in sediments of Dongping Lake,North China

Dongping Lake is an important regulator for the Eastern Route of South-to-North Water Diversion Project in China, and the water quality assurance of it is of great importance. To investigate the distribution characteristics and burial process of phosphorus (P) in Dongping Lake as well as their relationship with regional economic development and human activities, 33 spatially distributed surface sediment samples and one lake sediment core were extracted from Dongping Lake. A harmonized procedure for the P forms in freshwater sediments developed by the European Programme, Standards, Measurements, and Testing was used in this paper. The results show that NaOH–P (P bound to Al, Fe, Mn oxides or hydroxides), HCl–P (Ca-bound P), inorganic phosphorus (IP), organic phosphorus (OP), and total phosphorus (TP) in the surface sediments show a strong spatial variability. The highest NaOH–P and OP concentrations were observed in the eastern and south-eastern region of the lake and decreased gradually away from the mouth area of Dawen River. We deduced that anthropogenic input via the Dawen River is the main contributor. The higher concentration of HCl–P occurred in the north-west region of the lake and increased in a gradient away from the mouth area of Dawen River, and this pattern of distribution could be related to grain-size effects and higher transport energies close to riverine inlets. Pollution reflected by phosphorus in the core sediments of Dongping Lake is well consistent with the economic development history of Dongping County. From the beginning of the 20th century to the middle 1970s, the concentrations of each P speciation did not vary largely and runoff of the Yellow River mainly contributed to the P accumulation in the sediment, which might reflect the background values of them in the lake in pre-industrial period. The stable Mz (mean grain size), low loss-on-ignition (LOI), and high sedimentary flux also support this. The rapid increase of NaOH–P and OP at 10–0 cm (especially 5–0 cm) indicates the enhancing anthropogenic eutrophication since the middle 1970s. The LOI peak period and a coarsening of particle size also support this interpretation. However, the decreasing of TP and HCl–P was attributed to the change in sediment supply. As due to construction of dams around the lake, runoff of the Dawen River mainly contributed to the P accumulation in the sediment during this period.     

Structure and genesis of the Cubango Megafan in northern Namibia: implications for its hydrogeology

An exploration strategy for groundwater was established and followed in the northern Namibian Cuvelai-Etosha Basin (CEB). The data derived from transient electromagnetics, rotary-drilling, coring and sample investigation were used to refine stratigraphy and hydrostratigraphy, and to develop a 3D map of aquifers within the Cubango Megafan. The results have delineated three major aquifers. The newly found, deep-seated Ohangwena II Aquifer (KOH-2) has the potential of providing significant additional water to the water supply of northern Namibia and Angola. While near-surface aquifers carry predominantly brackish water, freshwater in the deep-seated aquifer is further extended and features good hydraulic properties. To date, only a small part of the hydrogeological potential of arid CEB has been explored and an extension of exploration is needed, including southern Angola. The combination of structural, sedimentological and hydrogeological approaches greatly advanced both the geological and hydrogeological understanding. With regard to the deep-seated aquifer, strict measures need to be applied to ensure that the water in the KOH-2 reservoir is exploited sustainably. Water control areas need to be established to ensure long-term preservation of this newly explored aquifer.     

Temporal and spatial patterns in abundance and diversity of fish assemblages in Elkhorn Slough,California

Assemblages of ichthyofauna of shallow inshore habitats along Californía’s central coast are described in terms of species composition, abundance, and life-style categories. A total of 22,334 fishes from 65 species and 27 families was collected with otter trawls at six sites in the main channel and tidal creeks of Elkhorn Slough, a tidal embayment and seasonal estuary, and two nearshore ocean stations in Monterey Bay during 44 months between August 1974 and June 1980. Greater than 90% of the catch comprised 10 species. The four dominant species,Cymatogaster aggregata, Leptocottus armatus, Phanerodon furcatus, andEmbiotoca jacksoni, occurred during most or all seasons and were classified as residents or partial residents. Several abundant species were marine immigrants that seasonally use the slough as spawning and nursery grounds; this resulted in higher abundance and species richness during summer. Species collected during winter largely were slough residents. Species compsosition and richness varied with distance from the slough entrance. The ocean assemblage was most different, and its similarity to other stations decreased progressively with distance inland and into the tidal creeks. During our study, 5,074 fishes were collected by beach seine in Bennett Slough, a remote shallow marsh basin adjacent to the entrance of Elkhorn Slough. Species richness was relatively low and three euryhaline species accounted for >80% of the total catch. The species assemblage was most similar to those at the tidal creek and most shallow stations of Elkhorn Slough. Resident species numerically dominated assemblages in Bennett Slough and the most inland areas of Elkhorn Slough. The high relative abundance of marine-related fishes (classified as marine, marine immigrant, and partial resident), entering Elkhorn Slough early in life or as spawning adults indicates the importance of this habitat to nearshore fish assemblages.     

Fractionation of sulfur isotopes during laboratory synthesis of pyrite at low temperatures

The reaction products and the accompanying sulfur isotope fractionations during the reaction of H₂S with goethite in aqueous media at 22–24°C for periods from 0.5 hr to 65 days were studied. Fine-grained pyrite formed within two days and was isotopically 0.8‰ lighter than the H₂S source. After 65 days reaction time the pyrite had nearly the same isotopic value as the H₂S. Aqueous precipitation of pyrite from H₂S and goethite at room temperature involved three major steps, namely: (1) the rapid oxidation of H₂S and reduction of Fe³⁺ during which elemental S is formed; (2) the formation of acid-volatile sulfides and the disappearance of elemental S; and (3) the formation of pyrite at the expense of acid-volatile sulfides.     

Biodegradation of benzo(a)pyrene mediated by catabolic enzymes of bacteria

An investigation was carried out to compare the ability of two bacteria Pseudomonas aeruginosa PSA5 and Rhodococcus sp. NJ2 isolated from petroleum sludge for degradation of benzo(a)pyrene [B(a)P], a HMW PAH compound in MSM. During 25 days of incubation, 50 ppm B(a)P was degraded by 88 and 47 % by P. aeruginosa PSA5 and Rhodococcus sp. NJ2, respectively. Besides, involvement of different catabolic enzymes, that is, salicylate hydroxylase, 2-carboxybenzaldehyde dehydrogenase, catechol 1,2-dioxygenase and catechol 2,3-dioxygenase, was also examined to identify their differential role in B(a)P degradation. Among these enzymes, the highest induction of 2-carboxybenzaldehyde dehydrogenase (773.5 nmol mg^?1 protein) was recorded in P. aeruginosa PSA5, while salicylate hydroxylase was highly expressed (839.6 nmol mg^?1 protein) in Rhodococcus sp. NJ2. Both the bacteria were found biosurfactant (glycolipid) producing, and role of biosurfactant in PAH degradation was also ascertained by reduced surface tension, higher emulsification index and increased cell surface hydrophobicity.     

Isotopic composition of rain- and groundwater at Mt. Vesuvius: environmental and volcanological implications

The present work reports on the isotopic characterization of rainfall and groundwater at Mt. Vesuvius. Values of δ ¹⁸O, monthly measured on rain samples collected during the period 2002–2004 in a rain-gauge network composed of 10 stations, were compared with meteorological and DEM data. Air temperature, controlled by the local orographic structure, was identified as the main factor influencing rain isotopic composition. Another important role is played by orographic clouds, whose condensation over the top of Mt. Vesuvius is responsible for anomalously high δ ¹⁸O values recorded in rain samples from the summit area of the volcanic edifice. A spatial model of rain isotopic composition, based on a 3D distribution of temperature derived by a 1 × 1 km DEM, was implemented and used for calculating the theoretical isotopic signature of seepage, further compared with data measured in the groundwater monitoring network. The analysis evidenced the role of local meteoric recharge as the main source feeding Mt. Vesuvius aquifers. The unique exception is the Olivella drainage gallery, located on the north-eastern flank of the volcanic edifice, whose isotopic composition is slightly more positive than the one expected for its altitude, likely caused by both evaporation processes and mixing with condensed hydrothermal vapor.     

A sulfur isotope study on pyrite deposits of Southern Tuscany,Italy

The S-isotope composition (δ³⁴S_CDT) of 213 samples of sulfides, sulfates and native sulfur from the pyrite mineralizations of southern Tuscany and associated country rocks were determined. The sulfur isotopic composition of pyrite is quite homogeneous and similar for all studied ore bodies, with an average δ³⁴S value near +9,5‰. Pyrite disseminated within the Filladi di Boccheggiano formation, and thought to be authigenic, shows a much larger range of δ³⁴S values (-13.1 to +14.5‰). The isotopic compositions of other sulfides associated with pyrite in the deposits show that isotopic equilibrium among sulfides was approached on a regional scale, but seldom fully attained. Isotopic data suggest that sedimentary marine sulfate was the ultimate source of sulfur in ores. Sulfates (mostly anhydrite) from the sulfate-carbonate lenses associated with both the Filladi di Boccheggiano and the Calcare Cavernoso formations also have similar and homogeneous compositions (average δ³⁴S=+15–16‰). Coexisting sulfates and sulfides are not in isotopic equilibrium. In the light of the isotopic data, among the many proposed genetic models for the largest stratabound pyrite bodies the two following alternatives appear the most likely: 1) in agreement with recently suggested hypotheses, the ore bodies are older than the emplacement of the Mio-Pliocenic granitoids in the area, and are probably hydrothermal-sedimentary in origin, coeval with associated country rocks; 2) the ore bodies were formed as a consequence of bacterial reduction of anhydrite in low-temperature convection systems related to the early stages of the Mio-Pliocenic thermal anomaly. In both cases, the emplacement of the Mio-Pliocenic granitoids caused metamorphism and remobilization of the pre-existing ores, producing smaller discordant mineralized bodies.     

Chloritization and its bearing on uranium mineralization in Madyalabodu area,Cuddapah district,Andhra Pradesh

Uranium mineralization in Madyalabodu area, Cuddapah district, Andhra Pradesh, is spatially related to chloritized and brecciated quartzite of the Gulcheru Formation in the immediate vicinity of E-W to ESE-WNW trending basic dyke. Chloritization transgresses the lithological boundaries. Whole-rock geochemical data indicate enrichment of MgO and Al₂O₃ coupled with depletion of SiO₂, Na₂O, K₂O, CaO and TiO₂ in the chlorite-rich zone. Fe₂O₃ and FeO do not vary significantly in the altered and the unaltered zones. Electron Probe Microanalysis (EPMA) data reveal that the chlorites in contact with uranium minerals are enriched in MgO and depleted in FeO than in the others. Considering the petrological evidence, geochemical signature and structural constraints, it appears that chlorite acted more as an adsorbent rather than as a reductant in facilitating uranium mineralization. Uraninite crystallized later from the uranium originally adsorbed on chlorites. Chloritization might also have facilitated mineralization through the generation of nascent hydrogen, H₂S and lowering pH of uranium-bearing solution.     

The accuracy with which coordinates of radio telescopes can be estimated using VLBI observations

Methods for external estimation of the accuracy of geodetic parameters (the coordinates of radio telescopes) based on VLBI observations are discussed. Time series of the distances between radio telescopes (baselines) provide the observational material for the analysis. It is shown that the generally accepted model for estimating the accuracy of geodetic results is based on unjustified assumptions, and does not adequately describe the results of geodetic observations. A more flexible parametrical model is proposed, which takes into account the non-uniformity in the accuracies with which geodetic parameters for different stations can be estimated, and more adequately describes the observational data. The evolution of the Svetloe-Badary and Zelenchuk-Badary baselines in 2007–2012 is analyzed in detail. The Badary VLBI station located near Irkutsk is moving away from the other two stations, located in the European part of Russia, at a rate of 3–4 mm/year.     

The long-term trends (1982–2006) in vegetation greenness of the alpine ecosystem in the Qinghai-Tibetan Plateau

The increased rate of annual temperature in the Qinghai-Tibetan Plateau exceeded all other areas of the same latitude in recent decades. The influence of the warming climate on the alpine ecosystem of the plateau was distinct. An analysis of alpine vegetation under changes in climatic conditions was conducted in this study. This was done through an examination of vegetation greenness and its relationship with climate variability using the Advanced Very High Resolution Radiometer satellite imagery and climate datasets. Vegetation in the plateau experienced a positive trend in greenness, with 18.0 % of the vegetated areas exhibiting significantly positive trends, which were primarily located in the eastern and southwestern parts of the plateau. In grasslands, 25.8 % of meadows and 14.1 % of steppes exhibited significant upward trends. In contrast, the broadleaf forests experienced a trend of degradation. Temperature, particularly summer temperature, was the primary factor promoting the vegetation growth in the plateau. The wetter and warmer climate in the east contributed to the favorable conditions for vegetation. The alpine meadow was mostly sensitive to temperature, while the steppes were sensitive to both temperature and precipitation. Although a warming climate was expected to be beneficial to vegetation growth in the alpine region, the rising temperature coupled with reduced precipitation in the south did not favor vegetation growth due to low humidity and poor soil moisture conditions.     

Formation of 35S-labelled elemental sulfur and pyrite in coastal marine sediments (Limfjorden and Kysing Fjord,Denmark) during short-term 35SO42− reduction measurements

Analyses of the specific products of ³⁵SO₄^2? reduction measurements were made in marine sediments in Denmark. We injected tracer quantities of ³⁵SO₄^2? into cores, incubated the cores, and assayed for ³⁵S-labelled acid volatile sulfides. Additionally, we assayed for ³⁵S-labelled elemental sulfur by extraction with CS₂, and for ³⁵S-labelled pyrite by reduction with chromium (II). We separately determined that elemental sulfur which formed in situ and that which formed by oxidation during the acid distillation of acid volatile sulfides.In subtidal sediments in Limfjorden, ³⁵S-labelled elemental sulfur and pyrite make up 14–32% of the reduced sulfur formed in short-term (0–48 hours) ³⁵SO₄^2? reduction experiments, at all depths studied (0–15 cm). Labelled elemental sulfur which formed in situ during the incubations at depths below 1 cm made up a fairly constant 5–11% of the total labelled reduced sulfur, from 0–1 cm, it made up 27%. An additional small amount (1–2% from 1–15 cm and 5% from 0–1 cm) of labelled elemental sulfur was formed during the acid-distillation step in our assay for labelled acid-volatile sulndes. Pyrite contained 4–13% of the total labelled reduced sulfur at all depths. Rates of sulfate reduction in Limfjorden were linear over the period 0–48 hours, and ³⁵S-pyrite made up a nearly constant percentage of the ³⁵S-labelled reduced sulfur formed over this time period.Estimates of sulfate reduction rates for Limfjorden which do not include elemental sulfur and pyrite as products are 19% too low. At Kysing Fjord, estimates of sulfate reduction which do not include elemental sulfur and pyrite are 24% to 32% too low. Thus, while previously published data on sulfate reduction in similar environments are probably low, they are not greatly in error.     

Simultaneous electrokinetic removal of polycyclic aromatic hydrocarbons and metals from a sediment using mixed enhancing agents

The maintenance of harbor waterways generates large amounts of dredged sediments which are often rich in coexisting organic and inorganic contaminants. Electrokinetic remediation treatments have recently been developed for the simultaneous removal of heavy metals and polycyclic aromatic hydrocarbons (PAHs), using various enhancing agents generally tested sequentially. In this study, different processing fluids were tested, alone or mixed, to improve the decontamination of aged model sediment contaminated with cadmium, lead, chromium, copper, zinc, and five PAHs. Nitric acid (NA) and citric acid (CA) were tested to avoid the formation of an alkaline front into the sediment and favor the metals removal, while an anionic surfactant [sodium dodecyl sulfate (SDS)] and a nonionic surfactant (Tween 20) were tested to solubilize and mobilize PAHs. Processing fluids were circulated under a constant voltage gradient of 1 V cm^?1 for 10–14 days. NA showed an excellent potential to remove metals (76.8–99.9 % removal) and PAHs (70.3–89.7 % removal) in a single run. Besides, the mixture of Tween 20 and CA, more environmental friendly, could be considered as a relatively good processing fluid for the simultaneous removal of metals (10.3–90.8 % removal) and PAHs (53.6–61.6 % removal) from the fine-grained sediment, while SDS mixed to CA was not a good candidate for this purpose (0.1–65 % removal for metals and 34.1–41.0 % removal for PAHs).     

Optimization of sample preparation method of total sulphur measurement in mine tailings

A sample preparation method of total sulphur measurement of reactive mine tailings was optimized. The total sulphur was measured by inductively coupled plasma optical emission spectroscopy, and ultrasound technique was used for sample digestion. The optimization process was adopted by a combined approach of experimental design and response surface methodology. The digestion time, temperature and acid-oxidant combination (i.e. effect of H₂O₂ with a fixed amount of acid mixture) were investigated. A two-level and three-factor (2³) full factorial design of experiment was applied to identify the most significant factors, and a central composite design was used to optimize the digestion procedure. KZK-1, a sericite schist, was selected as the certified reference material. The optimum methodology at 95 % confidence level (P < 0.05) was identified to be 10 min of digestion at 77 °C, with a solution of 1 ml HNO₃:1 ml HCl:1.35 ml H₂O₂. This combination resulted in 100 % sulphur recovery. The investigated method was verified by X-ray diffraction analysis. The optimum digestion level was applied to a reactive mine tailings, which achieved satisfactory results with a percentage relative standard deviation < 3 %.     

A comparative study of contaminant levels in Long Island Sound

This paper uses results from the National Oceanic and Atmospheric Administration’s National Status and Trends Program (NS&T) to place the environmental quality of Long Island Sound in a broader perspective. It compares levels of contaminants in blue mussels from ten Long Island Sound sites and in sediments from seven Long Island Sound sites with concentrations in the same media at 87 and 221 other sites, respectively, where comparable samples were obtained. In sediments, the levels of both trace metals and organic contaminants tend to be relatively high for Long Island Sound sites. This is especially true for five of the twelve metals (silver, cadmium, copper, lead, and zinc) and for five of six categories of organic contaminants (total chlordane, low molecular weight polycyclic aromatic hydrocarbons (PAHs), high molecular weight PAHs, total polychlorinated biphenyls, and total dichlorodiphenyltrichloroethanes). In mussels, the organic contaminant categories exhibit relatively high levels, but this is not true for most of the metals. In fact, four of the metals—arsenic, mercury, selenium, and zinc—show evidence of relatively low levels in mussels from Long Island Sound compared to other NS&T locations.     

Stratabound ore deposits related to synsedimentary tectonics: South-West Sardinia (Italy) and Sierra de Aracena (Spain); a comparison

Deposition of stratabound Zn-Pb-Ba ores in the Lower Cambrian carbonates in South-west Sardinia show a distinct relation with the prominent tensional tectonics in the area. A part of the mineral deposits are syngenetic (sedimentary-exhalative), other massive sulfides and/or barite are early diagenetic. Other occurrences (MVT) are from early to late-diagenetic. They are mostly confined to matrix- and cementbreccias which might be dependent on the Cambrian tectonics. The Precambrian-Lower Cambrian (?) carbonates occupying the core of the Aracena anticline, at the boundary between the provinces of Huelva and Badajoz (South-west Spain), are also an important metallotect for Zn-Pb-Ag-Ba mineralization. The ores at Aracena are stratabound (to stratiform) (Sedex) and occur as disseminations or layers in a volcano-sedimentary sequence with carbonate intercalations. Both the carbonate intervals and the ores show evidence of synsedimentary tectonics, like slumpings, slump breccias and neptunian dykes. Their deposition most likely occurred in a subtidal environment controlled by faults. Apparently, in South-west Sardinia and in the Sierra de Aracena, both sedimentary evolution and ore deposition were strictly related, and conditioned by several pulses of tensional tectonics.