Sr fluxes and isotopic compositions of the eleven rivers originating from the Qinghai-Tibet Plateau and their contributions to <Superscript>87</Superscript>Sr/<Superscript>86</Superscript>Sr evolution of seawater

To evaluate influence of chemical weathering of the Qinghai-Tibet Plateau (QTP) on seawater ⁸⁷Sr/⁸⁶Sr variation, river water and sediment samples were collected, and their Sr concentrations and isotopic compositions analyzed, from the seven large rivers that originated from the QTP. By combining these with the data of the Ganges, Brahmaputra, Indus and Irrawaddy originated in the southern QTP, the total Sr flux of the eleven rivers reaches 3.47×10⁹ mol·a⁻¹, which accounts for 10.2% of the total Sr flux transported by the global rivers. The weighted mean ⁸⁷Sr/⁸⁶Sr is 0.71694, higher than the average value of the global rivers. The ⁸⁷Sr_ex (⁸⁷Sr flux in excess of the seawater ⁸⁷Sr/⁸⁶Sr ratio) of the Chinese seven rivers is 1.55×10⁶ mol·a⁻¹, only accounting for about 6% of the value of the eleven rivers originated from QTP, and the Ganges-Brahmaputra system accounts for 86%. We assume that the QTP rivers have no strontium contributions to the oceans before ∼40 Ma and the Sr fluxes of the global rivers, except the QTP eleven rivers, are constant, then a maximum linear increase in Sr fluxes of the QTP rivers from zero to the modern value in response to tectonic uplift can explain ∼69% increase of seawater ⁸⁷Sr/⁸⁶Sr over the past ∼40 Ma and the remainder of 31% is perhaps provided from other factors. Supported by National Natural Science Foundation of China (Grant Nos. 40473009, 40331001, 40873001)     

On <Superscript>137</Superscript>Cs migration in water systems of Eastern Fennoscandia

The rate of natural removal of ¹³⁷Cs from water bodies in Eastern Fennoscandia is evaluated. The half-time T of water purification from global ¹³⁷Cs in lake–river systems was ~6.5 years and that for river systems was 6.5–10 years. For the 15- and 20-year exposure of ¹³⁷Cs in watershed soils, its annual input in rivers was 0.021–0.120 and 0.017–0.070% of its reserve. The period of May–December 1986 showed maximal export of ¹³⁷Cs, i.e., 1.1% of its reserve. ¹³⁷Cs export into rivers decreased in the region from north to south because of changes in landscape and climate conditions that affect ¹³⁷Cs migration on watersheds.     

<Superscript>40</Superscript>Ar/<Superscript>39</Superscript> Ar isotopic ages of Qitianling granite and their geologic implications

This paper has reported the first application of ⁴⁰Ar/³⁹ Ar dating to orthoclase from Qitianling granite. The resultant plateau ages yielded by three orthoclase specimens 2KL-17, 99LQ-2 and 2KL-31 (Note: The last one was taken from the part of granite which had been attributed to Cailing super-unit of the Indosinian Period by the former researchers) collected from the said granite are (139.57±2.79) Ma, (140.55±2.81) Ma and (144.91±2.90) Ma respectively. The above-mentioned ages represent the closed ⁴⁰Ar/³⁹ Ar age of the orthoclase. The consistency in age dating results, the similarity in geochemical characteristics and rock textures, and the NW-SE orientation of orthoclase phenocrysts almost throughout the granite, provide evidence for the intimate relationship between the Furong super-unit and the Cailing super-unit that form the main part of the granite, suggesting that they are products of comagmatic conjugate differentiation during the Late Jurassic. This paper also makes a comparison between the Qitianling granite and the Qianlishan granite.     

Weathering,Sr fluxes,and controls on water chemistry in the Lake Qinghai catchment,NE Tibetan Plateau

Strontium (Sr) concentrations and isotopic ratios have been measured in a series of water and rock samples from most of the major tributaries of the Lake Qinghai basin on the north‐eastern Tibetan Plateau. Dissolved Sr and ⁸⁷Sr/⁸⁶Sr show ranges of 488–12 240 nmol/l and 0·710497–0·716977, respectively. These data, together with measurements of major cations and anions in rivers and their tributaries and various lithologies of the catchment, were used to determine the contributions of Sr and its isotopic expense to rivers and lakes. Our results demonstrate that the chemical components and ⁸⁷Sr/⁸⁶Sr ratios of the alkaline waters are derived from mixing of carbonate and silicate sources, with the former contributing 72 ± 18% dissolved Sr to rivers. The difference in tributary compositions stems from the lithology of different river systems and low weathering intensity under a semi‐arid condition. Variation in ⁸⁷Sr/⁸⁶Sr ratios places constraint on the Sr‐isotopic compositions of the main tributaries surrounding Lake Qinghai. The water chemistry of the Buha River, the largest river within the catchment underlain by the late Paleozoic marine limestone and sandstones, dominates Sr isotopic composition of the lake water, being buffered by the waters from the other rivers and probably by groundwater. However, the characteristic chemical composition of the lake itself differs remarkably from the rivers, which can be attributed to precipitation of authigenic carbonates (low‐magnesium calcite, aragonite, and dolomite), though this does not impact the Sr isotope signature, which may remain a faithful indicator in paleo‐records. Regarding the potential role of groundwater input within the Lake Qinghai systems in the water budget and water chemistry, we have also determined the Sr concentration and ⁸⁷Sr/^S6Sr ratio of groundwater from diverse environments. This has allowed us to further constrain the Sr isotope systematic of this source. A steady‐state calculation gives an estimate for the groundwater flux of 0·19 ± 0·03 × 10⁸ m³/yr, accounting for about 8% of contemporary lake Sr budget. Copyright © 2010 John Wiley & Sons, Ltd.     

<Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar dating of the eruptive history of Mount Erebus,Antarctica: volcano evolution

Mt. Erebus, a 3,794-meter-high active polygenetic stratovolcano, is composed of voluminous anorthoclase-phyric tephriphonolite and phonolite lavas overlying unknown volumes of poorly exposed, less differentiated lavas. The older basanite to phonotephrite lavas crop out on Fang Ridge, an eroded remnant of a proto-Erebus volcano and at other isolated locations on the flanks of the Mt. Erebus edifice. Anorthoclase feldspars in the phonolitic lavas are large (~10 cm), abundant (~30–40%) and contain numerous melt inclusions. Although excess argon is known to exist within the melt inclusions, rigorous sample preparation was used to remove the majority of the contaminant. Twenty-five sample sites were dated by the ⁴⁰Ar/³⁹Ar method (using 20 anorthoclase, 5 plagioclase and 9 groundmass concentrates) to examine the eruptive history of the volcano. Cape Barne, the oldest site, is 1,311±16 ka and represents the first of three stages of eruptive activity on the Mt. Erebus edifice. It shows a transition from sub-aqueous to sub-aerial volcanism that may mark the initiation of proto-Erebus eruptive activity. It is inferred that a further ~300 ky of basanitic/phonotephritic volcanism built a low, broad platform shield volcano. Cessation of the shield-building phase is marked by eruptions at Fang Ridge at ~1,000 ka. The termination of proto-Erebus eruptive activity is marked by the stratigraphically highest flow at Fang Ridge (758±20 ka). Younger lavas (~550–250 ka) on a modern-Erebus edifice are characterized by phonotephrites, tephriphonolites and trachytes. Plagioclase-phyric phonotephrite from coastal and flank flows yield ages between 531±38 and 368±18 ka. The initiation of anorthoclase tephriphonolite occurred in the southwest sector of the volcano at and around Turks Head (243±10 ka). A short pulse of effusive activity marked by crustal contamination occurred ~160 ka as indicated by at least two trachytic flows (157±6 and 166±10 ka). Most anorthoclase-phyric lavas, characteristic of Mt. Erebus, are less than 250 ka. All Mt. Erebus flows between about 250 and 90 ka are anorthoclase tephriphonolite in composition.Editorial responsibility: J. Donelly-Nolan     

<Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar ages of the<Emphasis Type="Italic"> AD</Emphasis> 79 eruption of Vesuvius,Italy

The Italian volcano, Vesuvius, erupted explosively in AD 79. Sanidine from pumice collected at Casti Amanti in Pompeii and Villa Poppea in Oplontis yielded a weighted-mean ⁴⁰Ar/³⁹Ar age of 1925±66 years in 2004 (1σ uncertainty) from incremental-heating experiments of eight aliquants of sanidine. This is the calendar age of the eruption. Our results together with the work of Renne et al. (1997) and Renne and Min (1998) demonstrate the validity of the ⁴⁰Ar/³⁹Ar method to reconstruct the recent eruptive history of young, active volcanoes.     

First <Superscript>13</Superscript>C/<Superscript>12</Superscript>C isotopic characterisation of volcanic plume CO<Subscript>2</Subscript>

We describe analytical details and uncertainty evaluation of a simple technique for the measurement of the carbon isotopic composition of CO₂ in volcanic plumes. Data collected at Solfatara and Vulcano, where plumes are fed by fumaroles which are accessible for direct sampling, were first used to validate the technique. For both volcanoes, the plume-derived carbon isotopic compositions are in good agreement with the fumarolic compositions, thus providing confidence on the method, and allowing its application at volcanoes where the volcanic component is inaccessible to direct sampling. As a notable example, we applied the same method to Mount Etna where we derived a δ¹³C of volcanic CO₂ between −0.9 ± 0.27‰ and −1.41 ± 0.27‰ (Bocca Nuova and Voragine craters). The comparison of our measurements to data reported in previous work highlights a temporal trend of systematic increase of δ¹³C values of Etna CO₂ from ~ −4‰, in the 1970’s and the 1980’s, to ~ −1‰ at the present time (2009). This shift toward more positive δ¹³C values matches a concurrent change in magma composition and an increase in the eruption frequency and energy. We discuss such variations in terms of two possible processes: magma carbonate assimilation and carbon isotopic fractionation due to magma degassing along the Etna plumbing system. Finally, our results highlight potential of systematic measurements of the carbon isotopic composition of the CO₂ emitted by volcanic plumes for a better understanding of volcanic processes and for improved surveillance of volcanic activity.     

<Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar chronology and geochemistry of high-K volcanic rocks in the Mangkang basin,Tibet

Our two newly obtained high-quality ⁴⁰Ar/³⁹Ar ages suggest that the high-K volcanic rocks of the Lawuxiang Formation in the Mangkang basin, Tibet were formed at 33.5 ± 0.2 Ma. The tracing of elemental and Pb-Sr-Nd isotopic geochemistry indicates that they were derived from an EM2 enriched mantle in continental subduction caused by transpression. Their evidently negative anomalies in HFSEs such as Nb and Ta make clear that there is an input of continental material into the mantle source. The high-K rocks at 33.5 ± 0.2 Ma in the Mangkang basin may temporally, spatially and compositionally compare with the early one of two-pulse high-K rocks in eastern Tibet distinguished by Wang J. H. et al., implying that they were formed in the same tectonic setting.     

<Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar dating of tuff vents in the Campi Flegrei caldera (southern Italy): toward a new chronostratigraphic reconstruction of the Holocene volcanic activity

The Campi Flegrei hosts numerous monogenetic vents inferred to be younger than the 15 ka Neapolitan Yellow Tuff. Sanidine crystals from the three young Campi Flegrei vents of Fondi di Baia, Bacoli and Nisida were dated using ⁴⁰Ar/³⁹Ar geochronology. These vents, together with several other young edifices, occur roughly along the inner border of the Campi Flegrei caldera, suggesting that the volcanic conduits are controlled by caldera-bounding faults. Plateau ages of ∼9.6 ka (Fondi di Baia), ∼8.6 ka (Bacoli) and ∼3.9 ka (Nisida) indicate eruptive activity during intervals previously interpreted as quiescent. A critical revision, involving calendar age correction of literature ¹⁴C data and available ⁴⁰Ar/³⁹Ar age data, is presented. A new reference chronostratigraphic framework for Holocene Phlegrean activity, which significantly differs from the previously adopted ones, is proposed. This has important implications for understanding the Campi Flegrei eruptive history and, ultimately, for the evaluation of related volcanic risk and hazard, for which the inferred history of its recent activity is generally taken into account.     

Iron ions Fe<Superscript>2+</Superscript> and Fe<Superscript>3+</Superscript> in a magnetic model of the sedimentary medium

The concentration of rock-forming elements, the static magnetic susceptibility κ, spectra of electron paramagnetic resonance, and their relative intensities I are studied in samples from a borehole drilled in Cenozoic sedimentary deposits of southern Western Siberia. All measured values experience appreciable irregular variations with depth. A linear dependence exists between κ and I within the range of their medium and large values; κ and I have maximum values in the same sample, and κ_max = 1920 × 10^?6SI, κ_min = 210 × 10^?6 SI, and κ_av = 630 × 10^?6 SI. The magnetic properties of the samples are controlled by Fe²⁺ ions present in clastic material and by microphases (clusters) with Fe³⁺ ions of the goethite and lepidocrocite type present in the cement. The theoretically possible magnetic susceptibility of the Fe²⁺ ion system (provided that all iron exists in this form) is quite comparable with κ_min but, even with very high concentrations of Fe²⁺, does not reach half of κ_av: (154 < κ(Fe²⁺) < 254) × 10^?6 SI. Anomalously high values of κ are due to a large number of clusters with Fe³⁺ ions if structural units FeOOH do not dissociate and the interaction of the clusters with hydroxides of aluminum and precipitation medium impedes the process of their coagulation. Otherwise, the cluster sizes gradually increase, an antiferromagnetic structure develops in clusters, and the magnetic susceptibility decreases.     

Strontium in rivers of the Baltic Basin

The rivers in the Baltic Basin drain a mixture of bedrocks ranging from Mesozoic-Paleozoic sediments in the south to Proterozoic-Archean intrusives in the north. The rivers in the sedimentary basin in the south have high concentrations of Sr, in the interval 100–500 µg l^–1 while the⁸⁷Sr/⁸⁶Sr ratio is close to that of seawater, i.e. 0.71. The northern rivers in the Precambrian shield area on the other hand have low Sr concentrations of 15–50 µg l^–1 with high⁸⁷Sr/⁸⁶Sr ratios of about to 0.73 (0.721–0.745). The riverine input of dissolved Sr to the brackish Baltic Sea approaches 60 tons year^–1, with a weighted mean concentration approaching 130 µg l^–1 and a weighted mean⁸⁷Sr/⁸⁶Sr ratio close to 0.712. Although the sedimentary area in the south supplies only about 43% of the total river discharge, it gives about 88% of the total Sr input. Because of this and the strong regional riverine variation in⁸⁷Sr/⁸⁶Sr ratio, Sr and its isotopes seem to be a convenient tool to unveil mixing relations of water masses in the northern Baltic Sea, provided high resolution analyses are applied. For an overall characterization of water mixing in the Baltic Sea, the Nd system will be superior to that of Sr.     

The <Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar geochronology constraint and geological significance of mylonites in Shangyi-Chicheng fault belt on the north of North China Craton

A dating of two biotite samples taken from the meso- and low-temperature mylonites within the Shangyi-Chicheng fault belt on the north of the North China Craton yields ⁴⁰Ar/³⁹Ar isotopic ages of (399 ± 1) Ma and (263 ± 2) Ma, respectively. These data reflect an Early Devonian deformation and a Late Carboniferous retrograde metamorphism event along the fault, suggesting that the tectonic activities of the North China Craton in Paleozoic should be reconsidered.     

Distribution of <Superscript>226</Superscript>Ra in the Arctic Ocean and the Bering Sea and its hydrologic implications

Radium-226 (²²⁶Ra) activities were measured in the surface water samples collected from the Arctic Ocean and the Bering Sea during the First Chinese National Arctic Research Expedition. The results showed that ²²⁶Ra concentrations in the surface water ranged from 0.28 to 1.56 Bq/m³ with an average of 0.76 Bq/m³ in the Arctic Ocean, and from 0.25 to 1.26 Bq/m³ with an average of 0.71 Bq/m³ in the Bering Sea. The values were obviously lower than those from open oceans in middle and low latitudes, indicating that the study area may be partly influenced by sea ice meltwater. In the Bering Sea, ²²⁶Ra in the surface water decreased northward, probably as a result of the exchange between the ²²⁶Ra-deficient sea ice meltwater and the ²²⁶Ra-rich Pacific water. In the Arctic Ocean, ²²⁶Ra in the surface water increased northward and eastward. This spatial distribution of ²²⁶Ra reflected the variation of the ²²⁶Ra-enriched river component in the water mass of the Arctic Ocean. The vertical profiles of ²²⁶Ra in the Canadian Basin showed a concentration maximum at 200 m, which could be attributed to the inputs of the Pacific water or/and the bottom shelf water with high ²²⁶Ra concentration. This conclusion was consistent with the results from ²H, ¹⁸O tracers.     

Variations of <Emphasis Type="Italic">δ</Emphasis><Superscript>18</Superscript>O in precipitation from the Muztagata Glacier,East Pamirs

Expeditions to Muztagata (in the eastern Pamirs) during the summer seasons of 2002 and 2003 collected precipitation samples and measured their oxygen isotopes. The δ ¹⁸O in precipitation displays a wide range, varying from −17.40‰ to +1.33‰ in June-September 2002 and from −22.31‰ to +4.59‰ in May-August 2003. The δ ¹⁸O in precipitation correlates with the initial temperature of precipitation during the observing periods. The positive correlation between δ ¹⁸O and temperature suggests that δ ¹⁸O can be used as an indicator of temperature in this region. The δ ¹⁸O values in fresh-snow samples collected from two snow events at different elevations on the Muztagata Glacier show a strong “altitude effect”, with a ratio of nearly −0.40% per 100 m from 5500 m to 7450 m.     

Laser probe <Superscript>40</Superscript>Ar-<Superscript>39</Superscript>Ar ages of metasomatic K-feldspar from the Hougou gold deposit,northwestern Hebei Province,China

The Hougou gold deposit in northwestern Hebei is a typical K-metasomatism-related gold deposit hosted by K-altered rocks overprinting alkali intrusive rocks. In order to determine the age and pulse intervals of K-metasomatism in this gold deposit, some metasomatic K-feldspars from K-altered rocks are selected to measure their formation time by laser probe ⁴⁰Ar-³⁹Ar dating method. The new analyzing data show that these metasomatic K-feldspar formed during 202.6 Ma and 176.7 Ma, and the corresponding K-metasomatism and associated gold mineralization occurred in the early stage of Mesozoic era. The pulse intervals of K-metasomatism in the Hougou area are estimated to be about 4 Ma.     

<Superscript>137</Superscript>Cs in deep-water lakes: Analysis of the peculiarities of water contamination and purification

The assessment of ¹³⁷Cs concentration in water based on the model of radionuclide absorption by the bottom sediment of a closed water body is applicable to deep-water lakes with slower water circulation (the time of water exchange exceeding 10 years). The low river runoff from such lakes does not determine their water purification from ¹³⁷Cs because of the predominance of the process of ¹³⁷Cs sorption by suspension and bottom sediment. The contamination of a deep-water arctic lake with global ¹³⁷Cs is reconstructed.     

Source area and seasonal 87Sr/86Sr variations in rivers of the Amazon basin

We report the results of a detailed study of dissolved Sr isotopes in the Solimões and Beni‐Madeira Rivers of the Amazon basin. This study developed data collected over 8 years indicating large spatial and temporal variations in dissolved Sr isotopes among the rivers of the Amazon basin. The large ⁸⁷Sr/⁸⁶Sr variations were found to be correlated with the geology of the source areas of the suspended sediments. The Beni‐Madeira River displays a high average ⁸⁷Sr/⁸⁶Sr ratio and large ⁸⁷Sr/⁸⁶Sr fluctuations during the hydrological cycle. This large average value and fluctuations were related to the presence of Precambrian rocks and Ordovician sediments in the source area of the suspended sediment of the river. In contrast, the Solimões River displays a narrow range of Sr isotope ratio variations and an average value close to 0.709. This river drains mostly Phanerozoic rocks of northern Peru and Ecuador that are characterized by low Sr isotope ratios. The isotopic fluctuations in the Beni‐Madeira River were observed to propagate downstream at least as far as Óbidos. This signal is characterized by an inverse relationship between the concentration of elemental Sr and its isotopic ratios. We further demonstrate that the Sr isotopic composition and content in the Beni‐Madeira River is controlled by suspended sediments derived from the Andes. Despite draining areas underlain by Precambrian rocks and having high ⁸⁷Sr/⁸⁶Sr ratios, such rivers as the Negro and Tapajós play a minor role in the total Sr budget of the Amazon basin. Copyright © 2013 John Wiley & Sons, Ltd.     

Temporal variations in Sr and 87Sr/86Sr of the Ganga headwaters: estimates of dissolved Sr flux to the mainstream

The headwaters of the Ganga (the Alaknanda, Bhagirathi and the Ganga) were analysed for their dissolved major ions, Sr and ⁸⁷Sr/⁸⁶Sr on a biweekly to monthly basis over a period of one year to determine their temporal variations and the factors contributing to them. The concentrations of major ions and Sr show significant seasonal variation with lower values during monsoon period in all the three rivers. A similar trend is also observed for ⁸⁷Sr/⁸⁶Sr and Na*/Ca (Na* = Na_r? Cl_r) suggesting relatively lower contribution of Sr and Na from silicates (which are more radiogenic in Sr) during monsoon. Budget calculations show that silicate derived dissolved Sr (Sr_s) in the river Ganga, Alaknanda and the Bhagirathi varied from 10 ± 4 to 27 ± 11, 7 ± 3 to 30 ± 12, 16 ± 6 to 57 ± 23% of measured Sr respectively with lower values during monsoon. The relative decrease in silicate erosion compared to carbonate during monsoon can result from several factors, these include higher dissolution kinetics of the carbonates, lower water–rock interaction time and availability of larger area for weathering. The annual discharge weighted Sr flux derived from the time series data is higher by ～20% from that based on peak flow Sr, and lower by ～40% compared to that derived from lean flow Sr concentration. The area‐normalized annual flux of dissolved Sr from the Ganga at Rishikesh is about five times its flux at Rajshahi (Bangladesh) and a few other major global rivers, such as the Amazon, indicating higher erosion rate over the Himalaya. Copyright © 2010 John Wiley & Sons, Ltd.     

Distribution and significance of C~_(40) alkanes in the extracts of Cretaceous source rocks from the Songliao Basin

Source rock extracts and crude oils from the Songliao Basin were analyzed by high-temperature gas chromatography (HTGC), gas chromatography-mass spectrometry (HTGC-MS) and gas chromatography-isotope ratio-mass spectrometry (GC-IRMS), for high molecular-weight alkanes. The distributions of n-alkanes in the Nenjiang Formation extracts are in the C14―C63 range; a bimodal distribution occurs in the C-21 and C21―40 regions. The C30―C37 n-alkanes are accompanied by C29―C35 hopanes, whereas the high molecular-weight C45―C47 n-alkanes co-occur with abundant isoalkanes, alkylcyclohexanes and alkylcyclopentanes. The high δ 13C values of the n-alkanes and the microscopic maceral compositions indicate a highly diversified organic source input for the Nenjiang Formation source rocks, ranging from aquatic plants, blue alge-bacteria, to land plant material. In contrast, n-alkanes in the rock extracts of the Qingshankou Formation are characterized by a single modal distribution, with relatively low abundances of C29―C35 hopanes, but high molecular-weight isoalkanes, alkylcyclohexanes and alkylcyclopentanes. The relatively low δ 13C values of C22―C44 n-alkanes and organic material compositions indicate that the source rocks in the Qingshankou Formation contain dominantly type I algal organic matter. The relative abundance of C 40 compounds in source rocks changes little at low maturity stage, but decreases drastically at higher maturity levels, with a concurrent reduction in the odd/even carbon predominance. In crude oils, in contrast, the relative abundance of C 40 compounds appears to relate closely with the oil source and oil viscosity.