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1.
Na–HCO3–CO2-rich thermomineral waters issue in the N of Portugal, within the Galicia-Trás-os-Montes region, linked to a major NNE-trending fault, the so-called Penacova-Régua-Verin megalineament. Along this tectonic structure different occurrences of CO2-rich thermomineral waters are found: Chaves hot waters (67 °C) and also several cold (16.1 °C) CO2-rich waters. The δ2H and δ18O values of the thermomineral waters are similar to those of the local meteoric waters. The chemical composition of both hot and cold mineral waters suggests that water–rock reactions are mainly controlled by the amount of dissolved CO2 (g) rather than by the water temperature. Stable carbon isotope data indicate an external CO2 inorganic origin for the gas. δ13CCO2 values ranging between ? 7.2‰ and ? 5.1‰ are consistent with a two-component mixture between crustal and mantle-derived CO2. Such an assumption is supported by the 3He/4He ratios measured in the gas phase, are between 0.89 and 2.68 times the atmospheric ratio (Ra). These ratios which are higher than that those expected for a pure crustal origin (≈ 0.02 Ra), indicating that 10 to 30% of the He has originated from the upper mantle. Release of deep-seated fluids having a mantle-derived component in a region without recent volcanic activity indicates that extensive neo-tectonic structures originating during the Alpine Orogeny are still active (i.e., the Chaves Depression).  相似文献   

2.
The Chilean Patagonian fjords region (41–56°S) is characterized by highly complex geomorphology and hydrographic conditions, and strong seasonal and latitudinal patterns in precipitation, freshwater discharge, glacier coverage, and light regime; all of these directly affect biological production in the water column. In this study, we compiled published and new information on water column properties (primary production, nutrients) and surface sediment characteristics (biogenic opal, organic carbon, molar C/N, bulk sedimentary δ13Corg) from the Chilean Patagonian fjords between 41°S and 55°S, describing herein the latitudinal pattern of water column productivity and its imprint in the underlying sediments. Based on information collected at 188 water column and 118 sediment sampling sites, we grouped the Chilean fjords into four main zones: Inner Sea of Chiloé (41° to ～44°S), Northern Patagonia (44° to ～47°S), Central Patagonia (48–51°S), and Southern Patagonia (Magellan Strait region between 52° and 55°S). Primary production in the Chilean Patagonian fjords was the highest in spring–summer, reflecting the seasonal pattern of water column productivity. A clear north–south latitudinal pattern in primary production was observed, with the highest average spring and summer estimates in the Inner Sea of Chiloé (2427 and 5860 mg C m?2 d?1) and Northern Patagonia (1667 and 2616 mg C m?2 d?1). This pattern was closely related to the higher availability of nutrients, greater solar radiation, and extended photoperiod during the productive season in these two zones. The lowest spring value was found in Caleta Tortel, Central Patagonia (91 mg C m?2 d?1), a site heavily influenced by glacier meltwater and river discharge loaded with glacial sediments. Biogenic opal, an important constituent of the Chilean fjord surface sediments (SiOPAL ～1–13%), reproduced the general north–south pattern of primary production and was directly related to water column silicic acid concentrations. Surface sediments were also rich in organic carbon content and the highest values corresponded to locations far away from glacier influence, sites within fjords, and/or semi-enclosed and protected basins, reflecting both autochthonous (water column productivity) and allochthonous sources (contribution of terrestrial organic matter from fluvial input to the fjords). A gradient was observed from the more oceanic sites to the fjord heads (west–east) in terms of bulk sedimentary δ13Corg and C/N ratios; the more depleted (δ13Corg ?26‰) and higher C/N (23) values corresponded to areas close to rivers and glaciers. A comparison of the Chilean Patagonian fjords with other fjord systems in the world revealed high variability in primary production for all fjord systems as well as similar surface sediment geochemistry due to the mixing of marine and terrestrial organic carbon.  相似文献   

3.
SHRIMP zircon U–Pb dating, mineral chemical, element geochemical and Sr–Nd–Pb–Hf isotopic data have been determined for the Yulong monzogranite-porphyry in the eastern Tibet, China. The Yulong porphyry was emplaced into Triassic strata at about 39 Ma. The rocks are weakly peraluminous and show shoshonitic affinity, i.e., alkalis-rich, high K2O contents with high K2O / Na2O ratios, enrichment in LREE and LILE. They also show some affinities with the adakite, e.g., high SiO2 and Al2O3, and low MgO contents, depleted in Y and Yb, and enrichment in Sr with high Sr / Y and La / Yb ratios, and no Eu anomalies. The Yulong porphyry has radiogenic 87Sr / 86Sr (0.7063–0.7070) and unradiogenic 143Nd / 144Nd (εNd = − 2.0 to − 3.0) ratios. The Pb isotopic compositions of feldspar phenocrysts separated from the Yulong porphyry show a narrow range of 206Pb / 204Pb ratios (18.71–18.82) and unusually radiogenic 207Pb / 204Pb (15.65–15.67) and 208Pb / 204Pb (38.87–39.00) ratios. In situ Hf isotopic composition of zircons that have been SHRIMP U–Pb dated is characterized by clearly positive initial εHf values, ranging from + 3.1 to + 5.9, most between + 4 and + 5. Phenocryst clinopyroxene geothermometry of the Yulong porphyry indicates that the primary magmas had anomalously high temperature (> 1200 °C). The source depth for the Yulong porphyry is at least 100 km inferred by the metasomatic volatile phase (phlogopite–carbonate) relations. Detailed geochemical and Sr–Nd–Pb–Hf isotopic compositions not only rule out fractional crystallization or assimilation-fractional crystallization processes, but also deny the possibility of partial melting of subducted oceanic crust or basaltic lower crust. Instead, low degree (1–5%) partial melting of a metasomatized lithosphere (phlogopite–garnet clinopyroxenite) is compatible with the data. This example gives a case study that granite can be derived directly by partial melting of an enriched lithospheric mantle, which is important to understand the source and origin of diverse granites.  相似文献   

4.
The demand for clean water is on the increase as the population increases. One of the ways to address the water shortage is to treat the polluted water through removal of the contaminants. The use of adsorbents for pollutant removal is one of the promising methods. Seaweed is an aquatic plant and its sorption ability for selected metals in water was investigated in this study. We report the performance of the seaweed (Caulerpa serrulata) before and after modification with ethylenediamine (EDA), on adsorption of copper, lead and cadmium in aqueous solution. The adsorption capacities for Cu, Cd and Pb were 5.27 mg g−1, 2.12 mg g−1 and 2.16 mg g−1, respectively, with the EDA-modified seaweed, and 3.29 mg g−1, 4.57 mg g−1 and 1.06 mg g−1, with the unmodified weed, respectively. The pH for maximum adsorption was found to be within the range of pH 4–pH 6. In a separate investigation, it was found that 0.1 g of dried seaweed leached 20 mg of dissolved organic carbon (DOC) using 100 ml of distilled-deionised water. The resulting solution was green. The leaching phenomenon contributes to secondary pollution. Modification of the seaweed with EDA reduced the DOC content by half (50%) and also removed the green colouration. Kinetic studies showed that the adsorbent was able to take up to 95% of the metals (in synthetic standard solutions) in less than 10 min. The adsorbed metals were then stripped using a solution of 0.5 M HNO3 indicating that the adsorbent can be regenerated. In addition, the study revealed that modification improved the thermal stability of the adsorbent such that even when the temperature was raised to 1000 °C, more than 80% (compared to <50% for unmodified weed) of the modified adsorbent was not degraded, indicating that modification had a significant influence on the thermal stability of seaweed. The modified seaweed has been shown to have great potential for the removal of metals and DOC in polluted water. The modified adsorbent can therefore be applied for the removal of metals in polluted waters hence suitable for treatment of water for domestic consumption at a point of use.  相似文献   

5.
《Marine pollution bulletin》2012,64(5-12):201-208
Flow cytometry was used to examine immune responses in haemocytes of the green-lipped mussel Perna viridis under six combinations of oxygen level (1.5 mg O2 l−1, 6.0 mg O2 l−1) and temperature (20 °C, 25 °C and 30 °C) at 24 h, 48 h, 96 h and 168 h. The mussels were then transferred to normoxic condition (6.0 mg O2 l−1) at 20 °C for further 24 h to study their recovery from the combined hypoxic and temperature stress. Esterase (Est), reactive oxygen species (ROS), lysosome content (Lyso) and phagocytosis (Pha) were reduced at high temperatures, whereas hypoxia resulted in higher haemocyte mortality (HM) and reduced phagocytosis. For HM and Pha, changes were observed after being exposed to the stresses for 96 h, whereas only a 24 h period was required for ROS and Lyso, and a 48 h one for Est. Recovery from the stresses was observed for HM and Pha but not other immune responses.  相似文献   

6.
Os–Hf–Sr–Nd isotopes and PGE were determined in peridotite xenoliths carried to the surface by Quaternary alkali basaltic magmas in the Tokinsky Stanovik Range on the Aldan shield. These data constrain the timing and nature of partial melting and metasomatism in the lithospheric mantle beneath SE Siberian craton. The xenoliths range from the rare fertile spinel lherzolites to the more abundant, strongly metasomatised olivine-rich (70–84%) rocks. Hf–Sr–Nd isotope compositions of the xenoliths are mainly within the fields of oceanic basalts. Most metasomatised xenoliths have lower 143Nd / 144Nd and 176Hf / 177Hf and higher 87Sr / 86Sr than the host basalts indicating that the metasomatism is older and has distinct sources. A few xenoliths have elevated 176Hf / 177Hf (up to 0.2838) and plot above the Hf–Nd mantle array defined by oceanic basalts.187Os / 188Os in the poorly metasomatised, fertile to moderately refractory (Al2O3 ≥ 1.6%) Tok peridotites range from 0.1156 to 0.1282, with oldest rhenium depletion ages being about 2 Ga. The 187Os / 188Os in these rocks show good correlations with partial melting indices (e.g. Al2O3, modal cpx); the intercept of the Al–187Os / 188Os correlation with lowest Al2O3 estimates for melting residues (∼0.3–0.5%) has a 187Os / 188Os of ∼0.109 suggesting that these peridotites may have experienced melt extraction as early as 2.8 Gy ago. 187Os / 188Os in the strongly metasomatised, olivine-rich xenoliths (0.6–1.3% Al2O3) ranges from 0.1164 to 0.1275 and shows no apparent links to modal or chemical compositions. Convex-upward REE patterns and high abundances of heavy to middle REE in these refractory rocks indicate equilibration with evolved silicate melts at high melt / rock ratios, which may have also variably elevated their 187Os / 188Os. This inference is supported by enrichments in Pd and Pt on chondrite-normalised PGE abundance patterns in some of the rocks. The melt extraction ages for the Tok suite of 2.0 to 2.8 Ga are younger than oldest Os ages reported for central Siberian craton, but they must be considered minimum estimates because of the extensive metasomatism of the most refractory Tok peridotites. This metasomatism could have occurred in the late Mesozoic to early Cenozoic when the Tok region was close to the subduction-related Pacific margin of Siberia and experienced large-scale tectonic and magmatic activity. This study indicates that metasomatic effects on the Re–Os system in the shallow lithospheric mantle can be dramatic.  相似文献   

7.
Aluminum incorporation into the high pressure polymorph of TiO2 with the structure of α-PbO2 has been studied from 10 to 20 GPa and 1300 °C by XRD, high-resolution 27Al MAS-NMR and TEM. Al-doped α-PbO2 type TiO2 can be recovered at atmospheric pressure. Al2O3 solubility in α-PbO2 type TiO2 increases with increasing the synthesis pressure. The α-PbO2 type TiO2 polymorph is able to incorporate up to 35 wt.% Al2O3 at 13.6 GPa and 1300 °C, being the substitution of Ti4+ by Al3+ on normal octahedral sites the mechanism of solubility. The transition to the higher pressure TiO2 polymorph with the ZrO2 baddeleyite structure, Akaogiite, has not been observed in the quenched samples at room pressure. The microstructure of the recovered sample synthesized at 16 GPa and 1300 °C points to the existence of a non-quenchable aluminum titanium oxide phase at these conditions.  相似文献   

8.
The UV camera is becoming an important new tool in the armory of volcano geochemists to derive high time resolution SO2 flux measurements. Furthermore, the high camera spatial resolution is particularly useful for exploring multiple-source SO2 gas emissions, for instance the composite fumarolic systems topping most quiescent volcanoes. Here, we report on the first SO2 flux measurements from individual fumaroles of the fumarolic field of La Fossa crater (Vulcano Island, Aeolian Island), which we performed using a UV camera in two field campaigns: in November 12, 2009 and February 4, 2010. We derived ~ 0.5 Hz SO2 flux time-series finding fluxes from individual fumaroles, ranging from 2 to 8.7 t d?1, with a total emission from the entire system of ~ 20 t d?1 and ~ 13 t d?1, in November 2009 and February 2010 respectively. These data were augmented with molar H2S/SO2, CO2/SO2 and H2O/SO2 ratios, measured using a portable MultiGAS analyzer, for the individual fumaroles. Using the SO2 flux data in tandem with the molar ratios, we calculated the flux of volcanic species from individual fumaroles, and the crater as a whole: CO2 (684 t d?1 and 293 t d?1), H2S (8 t d?1 and 7.5 t d?1) and H2O (580 t d?1 and 225 t d?1).  相似文献   

9.
We investigated the provenance of organic matter in the inner fjord area of northern Patagonia, Chile (～44–47°S), by studying the elemental (organic carbon, total nitrogen), isotopic (δ13C, δ15N), and biomarker (n-alkanoic acids from vascular plant waxes) composition of surface sediments as well as local marine and terrestrial organic matter. Average end-member values of N/C, δ13C, and δ15N from organic matter were 0.127±0.010, ?19.8±0.3‰, and 9.9±0.5‰ for autochthonous (marine) sources and 0.040±0.018, ?29.3±2.1‰, and 0.2±3.0‰ for allochthonous (terrestrial) sources. Using a mixing equation based on these two end-members, we calculated the relative contribution of marine and terrestrial organic carbon from the open ocean to the heads of fjords close to river outlets. The input of marine-derived organic carbon varied widely and accounted for 13–96% (average 61%) of the organic carbon pool of surface sediments. Integrated regional calculations for the inner fjord system of northern Patagonia covered in this study, which encompasses an area of ～4280 km2, suggest that carbon accumulation may account for between 2.3 and 7.8×104 ton C yr?1. This represents a storage capacity of marine-derived carbon between 1.8 and 6.2×104 ton yr?1, which corresponds to an assimilation rate of CO2 by marine photosynthesis between 0.06 and 0.23×106 ton yr?1. This rate suggests that the entire fjord system of Patagonia, which covers an area of ～240,000 km2, may represent a potentially important region for the global burial of marine organic matter and the sequestration of atmospheric CO2.  相似文献   

10.
New trace element and Hf, Nd, and Pb isotope data are reported for 22 basalts collected between 22°N and 35°N on the Mid-Atlantic Ridge. (La / Sm)N ratios identify the presence of enriched (E)-MORB in the northernmost part of this area and normal (N)-MORB elsewhere. A negative correlation is observed when 143Nd / 144Nd is plotted against 206Pb / 204Pb, 207Pb / 204Pb, and 208Pb / 204Pb, whereas 176Hf / 177Hf appears not to correlate with any of the other isotopic ratios. The E-MORB samples are characterized by high 206Pb / 204Pb, 207Pb / 204Pb, 208Pb / 204Pb, and low 143Nd / 144Nd. Principal Component Analysis (PCA) of Pb isotopes alone identifies three, and only three, significant geochemical end-members (‘components’). Including Nd and Hf isotopic data in the PCA produces spurious components, partly because of curved mixing relationships, and partly because of fractionation during melting. Our preferred interpretation of why 176Hf / 177Hf is decoupled from the other isotopic ratios is, as inferred from recent experimental data, that the Hf isotopic compositions of the melt and the residue fail to equilibrate during melting. A strong correlation between (Sr / Nd)N and (Eu / Eu*)N indicates that plagioclase is a residual phase of N-MORB, but not of E-MORB melting. The three end-members identified in this study are the depleted mantle, a common-type component, and an enriched plume-type end-member. The common, or ‘C’-type, end-member is characteristic of E-MORB and may itself be a mixture containing recycled oceanic crust (the MORB suite, terrigenous sediments, and/or oceanic plateaus). The plume-type end-member is likely to represent the lower mantle and may involve some primordial material. It is shown that mantle isochrons in general and the Pb–Pb isochron in particular do not characterize a specific geodynamic process acting to create mantle heterogeneities.  相似文献   

11.
Soda lakes and pans represent saline ecosystems with unique chemical composition, occurring on all continents. The purpose of this study was to identify and characterise the main environmental gradients and trophic state that prevail in the soda pans (n = 84) of the Carpathian Basin in Central Europe. Underwater light conditions, dissolved organic matter, phosphorus and chlorophyll a were investigated in 84 pans during 2009–2010. Besides, water temperature was measured hourly with an automatic sensor throughout one year in a selected pan. The pans were very shallow (median depth: 15 cm), and their extremely high turbidity (Secchi depth median: 3 cm, min: 0.5 cm) was caused by high concentrations of inorganic suspended solids (median: 0.4 g L−1, max: 16 g L−1), which was the dominant (>50%) contributing factor to the vertical attenuation coefficient in 67 pans (80%). All pans were polyhumic (median DOC: 47 mg L−1), and total phosphorus concentration was also extremely high (median: 2 mg L−1, max: 32 mg L−1). The daily water temperature maximum (44 °C) and fluctuation maximum (28 °C) were extremely high during summertime. The combination of environmental boundaries: shallowness, daily water temperature fluctuation, intermittent hydroperiod, high turbidity, polyhumic organic carbon concentration, high alkalinity and hypertrophy represent a unique extreme aquatic ecosystem.  相似文献   

12.
In situ LA-ICPMS U-Pb, trace element, and Hf isotope data in zircon demonstrate a Carboniferous age for eclogite-facies metamorphism in Siluro-Devonian protoliths in the Huwan shear zone, Dabie Mountains, Central China. This age contrasts with the more prevailing Triassic age for high- to ultrahigh pressure (HP to UHP) metamorphism in the Qinling-Dabie-Sulu orogen. Metamorphic zircon in two eclogite samples from Sujiahe is characterized by low Th/U ratios, small negative Eu anomalies, flat HREE patterns, and low 176Lu/177Hf ratios. These geochemical signatures suggest that the zircon crystallized in the presence of garnet and in the absence of plagioclase feldspar. Furthermore, temperatures of ~ 655 and ~ 638 °C, calculated using the Ti content of zircon, are consistent with their formation during eclogite-facies metamorphism. The weighted mean 206Pb/238U age of 309 ± 4 Ma (2δ) for this zircon improves previous age estimates for eclogite-facies metamorphism in the Huwan shear zone, ranging from 420 to 220 Ma. Metamorphic zircon from one eclogite sample from Hujiawan, most likely formed during prograde metamorphism, yields an equivalent age estimate of 312 ± 11 Ma. Magmatic zircon cores in the three samples yield ages for the magmatic protoliths of the eclogites ranging from 420 ± 7 to 406 ± 5 Ma, and post-dating the middle Paleozoic collision of the North China and the Qinling terrain. The zircon crystals in the three eclogite samples display a large variation of εHf (t) values of ? 4.9 to 21.3. The metamorphic zircon overgrowths show the same range of εHf (t) values as those of the inherited magmatic crystal interiors. This suggests that the metamorphic zircon overgrowths may have formed by dissolution-reprecipitation of pre-existing magmatic zircon thereby preserving their original Hf isotopic composition. The high εHf (t) values suggest that the protoliths were derived from depleted mantle sources, most likely Paleotethyan oceanic crust; while the low εHf (t) values are attributed to crustal contamination. Some eclogites in the Huwan shear zone have a distinctive signature of continental crust most probably derived from the Yangtze Craton. The coexistence of Paleozoic oceanic crust and Neoproterozoic continental crust with similar metamorphic ages in the Huwan shear zone implies that Paleozoic Paleotethyan oceanic crust was produced within a marginal basin of the northern Yangtze Craton. The opening of the Paleo-Tethyan ocean was slightly younger than the collision of the North China Craton and the Qinling terrain during the Late Paleozoic in the Qinling-Dabie-Sulu orogen. Subduction of the Paleo-Tethyan oceanic crust and associated continental basement resulted in the 309 ± 2 Ma (2σ) eclogite-facies metamorphism in the Huwan shear zone. The subsequent Triassic continent-continent collision led to the final coalescence of the Yangtze and Sino-Korean cratons. Amalgamation of the Yangtze and North China cratons was, therefore, a multistage process extending over at least 200 Ma.  相似文献   

13.
《Marine pollution bulletin》2012,64(5-12):523-527
Concentrations of trace metals (Zn, Cr, Cu, V, Cd and Pb), total organic carbon (TOC), black carbon (BC) and their granulometry were examined in 25 surface sediment samples from the northern Bering Sea, Chukchi Sea and adjacent areas. Trace metal concentrations in the sediments varied from 21.06–168.21 mg kg−1 for Zn, 8.91–46.94 mg kg−1 for Cr, 2.69–49.39 mg kg−1 for Cu, 32.46–185.54 mg kg−1 for V, 0.09–0.92 mg kg−1 for Cd, and 0.95–15.25 mg kg−1 for Pb. The geoaccumulation index (Igeo) indicated that trace metal contamination (Zn and Cd) existed in some stations of the study area. The distribution of grain size plays an important role in influencing the distribution of trace metals (Zn, Cr, Cu, V, and Pb) in sediments from the Chukchi Sea and adjacent areas.  相似文献   

14.
Investigations to understand linkages among climate, erosion and weathering are central to quantifying landscape evolution. We approach these linkages through synthesis of regolith data for granitic terrain compiled with respect to climate, geochemistry, and denudation rates for low sloping upland profiles. Focusing on Na as a proxy for plagioclase weathering, we quantified regolith Na depletion, Na mass loss, and the relative partitioning of denudation to physical and chemical contributions. The depth and magnitude of regolith Na depletion increased continuously with increasing water availability, except for locations with mean annual temperature < 5 °C that exhibited little Na depletion, and locations with physical erosion rates < 20 g m? 2 yr? 1 that exhibited deep and complete regolith Na depletion. Surface Na depletion also tended to decrease with increasing physical erosion. Depth-integrated Na mass loss and regolith depth were both three orders of magnitude greater in the fully depleted, low erosion rate sites relative to other locations. These locations exhibited strong erosion-limitation of Na chemical weathering rates based on correlation of Na chemical weathering rate to total Na denudation. Sodium weathering rates in cool locations with positive annual water balance were strongly correlated to total Na denudation and precipitation, and exhibited an average apparent activation energy (Ea) of 69 kJ mol? 1 Na. The remaining water-limited locations exhibited kinetic limitation of Na weathering rates with an Ea of 136 kJ mol? 1 Na, roughly equivalent to the sum of laboratory measures of Ea and dissolution reaction enthalpy for albite. Water availability is suggested as the dominant factor limiting rate kinetics in the water-limited systems. Together, these data demonstrate marked transitions and nonlinearity in how climate and tectonics correlate to plagioclase chemical weathering and Na mass loss.  相似文献   

15.
We report observations of seasonal and local time variation of the averaged electron and iron concentrations, as well as simultaneous measurements of the two species, above the Arecibo Observatory (18.35°N, 66.75°N), Puerto Rico. The average Fe profile between 21:00 and 24:00 LT has a single peak at about 85 km with the exception of the summer when an additional peak exists at about 95 km. The higher Fe peak in the summer is correlated with higher electron concentrations in this season. The three nights of simultaneous measurements of electron and iron concentrations show that narrow layers of Fe and electrons are well correlated. Comparison of the climatological and simultaneous Fe and electron data suggests that recombination of Fe+ plays an important role in determining the Fe profile in the upper part of the Fe layer. Above 93 km, the Fe concentration appears to increase after sunset if the electron concentration exceeds about 4000 electrons cm−3. The average rate of Fe production is about 0.1 atom cm−3 s−1 for all seasons at 100 km in the early evening hours. A chemical model reveals that the concentration of Fe+ must be 50–80% of the total ionization over Arecibo for typical equinox conditions to explain the observed rate of Fe production. These high relative Fe+ concentrations are consistent with in situ observations that Fe+ is usually the dominant ion in sporadic E layers in the nighttime lower E region. This suggests that the source of Fe+ is provided by sporadic E layers descending over Arecibo after sunset. The Fe density between 80 and 85 km decreases during the night, for all seasons. This is attributed to the formation of stable molecular Fe species, such as FeOH, due to the increase in O3 and decrease in atomic O and H during the night at these altitudes.  相似文献   

16.
We present the new 14C extraction line at ETH Zürich. This system is designed to extract in situ-produced cosmogenic 14C from terrestrial quartz samples, and to obtain pure CO2 gas for analysis with a gas ion source Accelerator Mass Spectrometry (AMS) system. Samples are degassed at 1550–1600 °C without the use of a fluxing agent. Gas purification is achieved by a series of cryogenic traps and passage through hot Ag and Cu wool/mesh. Graphitization and, thus, sample dilution is not required. Tests to determine the CO2 recovery after gas extraction and cleaning yielded consistently good recovery rates of >99.8% (n = 7). The 14C blank contribution from the all-metal tubing system is negligible. Our preliminary procedural blank estimate – deriving mostly from the hot extraction furnace – is <5 × 105 14C atoms. Extraction tests on two quartz samples by stepped-heating show a quantitative separation of atmospheric 14C at ≤500 °C from the in situ component above 1200 °C. Based on these data, we estimate to achieve a complete 14C extraction from a quartz sample.  相似文献   

17.
Adsorption of Pb2+ from aqueous solution onto a sugarcane bagasse/multi-walled carbon nanotube (MWCNT) composite was investigated by using a series of batch adsorption experiments and compared with the metal uptake ability of sugarcane bagasse. The efficiency of the adsorption processes was studied experimentally at various pH values, contact times, adsorbent masses, temperatures and initial Pb2+ concentrations. A pH of 4.5 was found to be the optimum pH to obtain a maximum adsorption percentage in 120 min of equilibration time. The composite showed a much enhanced adsorption capacity for Pb2+ of 56.6 mg g−1 compared with 23.8 mg g−1 for bagasse at 28 °C. The Langmuir adsorption isotherm provided the best fit to the equilibrium adsorption data. The pseudo first-order, pseudo second-order, intraparticle diffusion and Elovich kinetics models were used to analyse the rate of lead adsorption and the results show that the Elovich model is more suitable. The thermodynamic parameters of adsorption, namely ΔG°, ΔH° and ΔS°, were determined over the temperature range of 20–45 °C. The adsorption of Pb2+ onto both bagasse and the sugarcane bagasse/MWCNT composite was found to be spontaneous but for the former adsorbent it was enthalpy-driven whereas for the latter it was entropy-driven. Desorption of the lead-loaded adsorbents was fairly efficient with 0.1 mol dm−3 HCl. Overall this composite has the potential to be a good adsorbent for the removal of Pb2+ from wastewaters.  相似文献   

18.
We present molybdenum isotope data for four sediment profiles from continental margin settings. Each profile has a distinctive average isotope composition ranging from δ98 / 95Mo − 0.5‰ to 1.3‰ (relative to J and M laboratory standard). This range lies between the modern ocean water value (2.3‰) and the values typical of Mo adsorbed onto Mn oxides (− 0.7‰ ± 0.1‰). An important finding of this study is the apparent co-variation between the Mo isotope composition and the accumulation rate of authigenic Mo under reducing conditions. This relationship suggests that the chemical processes responsible for Mo accumulation under reducing conditions produce an isotope signature in marine sediments. In addition to the relationship between Mo accumulation and the Mo isotope signature there is also a relationship between these parameters and the rate of organic carbon oxidation and burial. These relationships suggest that the Mo isotope signature of reducing sediments may serve as a tracer for the cycling of organic carbon in continental margin sediments; however, additional data will be required to refine any such relationships.  相似文献   

19.
《Marine pollution bulletin》2009,58(6-12):867-872
Sediment sampled from Taichung Harbor was mixed with local reservoir sediment at different weight ratios to prepare lightweight aggregate at 1050, 1100, and 1150 °C. A pressure of 3000 or 5000 psi was used to shape the powder mixtures into pellets before the heating processes. The results indicate that the leaching levels of trace metals from the lightweight aggregate samples are considerably reduced to levels less than Taiwan Environmental Protection Administration regulatory limits. Increasing final process temperature tends to reduce the bulk density and crushing intensity of lightweight aggregate with a concomitant increase in water sorption capability. Lightweight aggregate with the lowest bulk density, 0.49 g cm−3 for the 5000 psi sample, was obtained with the heating process to 1150 °C. Based on the X-ray absorption near edge structure results, FeSO4 decomposition with a concomitant release of SOx (x = 2, 3) is suggested to play an important role for the bloating process in present study.  相似文献   

20.
Sampling and analyses methods for determining the stable isotopic compositions of Hg in an active volcanic system were tested and optimized at the volcanic complex of Vulcano (Aeolian Islands, Italy). Condensed gaseous fumarole Hg(fum)T, plume gaseous elemental Hg(g)0 and plume particulate Hg(p)II were obtained at fumaroles F0, F5, F11, and FA. The average total Hg emissions, based on HgT/SO2 in condensed fumarolic gases and plumes, range from 2.5 to 10.1 kg y? 1, in agreement with published values [Ferrara, R., Mazzolai, B., Lanzillotta, E., Nucaro, E., Pirrone, N., 2000. Volcanoes as emission sources of atmospheric mercury in the Mediterranean Basin. Sci. Total Environ. 259(1–3), 115–121; Aiuppa, A., Bagnato, E., Witt, M.L.I., Mather, T.A., Parello, F., Pyle, D.M., Martin, R.S., 2007. Real-time simultaneous detection of volcanic Hg and SO2 at La Fossa Crater, Vulcano (Aeolian Islands, Sicily). Geophys. Res. Lett. 34(L21307).]. Plume Hg(p)II increases with distance from the fumarole vent, at the expense of Hg(g)0 and indicates significant in-plume oxidation and condensation of fumarole Hg(fum)T.Relative to the NIST SRM 3133 Hg standard, the stable isotopic compositions of Hg are δ202Hg(fum)T = ? 0.74‰ ± 0.18 (2SD, n = 4) for condensed gaseous fumarole Hg(fum)T, δ202Hg(g)0 = ? 1.74‰ ± 0.36 (2SD, n = 1) for plume gaseous elemental Hg(g)0 at the F0 fumarole, and δ202Hg(p)II = ? 0.11‰ ± 0.18 (2SD, n = 4) for plume particulate Hg(p)II. The enrichment of Hg(p)II in the heavy isotopes and Hg(g)0 in the light isotopes relative to the total condensed fumarolic Hg(fum)T gas complements the speciation data and demonstrates a gas-particle fractionation occurring after the gas expulsion in ambient T° atmosphere. A first order Rayleigh equilibrium condensation isotope fractionation model yields a fractionation factor αcond-gas of 1.00135 ± 0.00058.  相似文献   

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