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.     

Granitic plutonism as an indicator of microplates in the Palaeozoic of central and eastern Maine

Oxygen and strontium isotope ratios have been used to characterize source regions for granitic magmas for a transect across the northern Appalachian orogen in central and eastern Maine. The northwestern plutons (Katahdin and Seboeis) have δ¹⁸O values of 10.3–13.3 and initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7083 and 0.7066, respectively. The central plutons (Bottle Lake and Center Pond) have lower δ¹⁸O values (8.2–9.9) and initial ⁸⁷Sr/⁸⁶Sr ratios (0.7043–0.7055). The southeastern plutons (Lucerne and Deblois) have δ¹⁸O values (9.0–11.0) but initial ⁸⁷Sr/⁸⁶Sr ratios (0.7077 and 0.7041, respectively) which are intermediate between the northwestern and central plutons.Source models derived from these results and other petrological and geochemical data reflect the juxtaposition of discrete source regions by transcurrent faulting, which may be related to oblique plate motions. This model illustrates the importance of microplate accretion in the Palaeozoic history of the northern Appalachian orogen.     

Distribution and content of different artifical radio nuclides in the water of the North Sea during the years 1977 to 1981 (complemented with some results from 1982 to 1984)

Summary The measured concentrations of¹³⁷Cs in the water of the North Sea gained during the years 1977 to 1982 largely confirm the results found in the preceding years (Fig. 1). After a distinct maximum in 1978 — brought about by a particularly strong influx during 1977 — the total quantity of¹³⁷Cs present in the North Sea has reced, to around half of these peak values by the year 1982 (Table 1).On the way from the Sellafield Works near the Irish Sea as far as into the North Sea, a strong shift of the¹³⁷Cs:⁹⁰Sr ratio in favour of the⁹⁰Sr can be observed.By following the temporal course of that ratio at different measurement points, a transport time can be deduced of around 3 years between the Sellafield Works and the Pentland Firth; a further year would be needed to reach into the southeastern North Sea.The ratio Cs:Sr furthermore permits, in the southeastern North Sea, a good distinction between the watermasses comming from the north into the North Sea with respect to those that come through the Channel from the South. These masses practically flow side by side until about the entrance to the Skagerrak.The vertical distribution of the¹³⁷Cs shows, as is to be expected, seasonally conditioned differences. However, effects also occur, which — on the basis of the data available to date — do not yet permit a clear explanation.The⁹⁰Sr, as well as the^239+240Pu, present in the North Sea show an analogous distribution scheme compared with that of the¹³⁷Cs. Their concentrations lie far below that of the¹³⁷Cs (⁹⁰Sr 17.5%;^239+240Pu 0.03%).Tritium, on the other hand — with essentially higher concentrations — shows a completely different distribution, because it is principly introduced via the freshwater flowing in from the land.

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Verteilung und Gehalt verschiedener künstlicher Radionuklide im Wasser der Nordsee in den Jahren 1977 bis 1981 (ergänzt durch einige Ergebnisse von 1982 bis 1984)

Zusammenfassung Die in den Jahren 1977 bis 1982 gewonnenen Meßdaten der Aktivitätskonzentrationen von¹³⁷Cs im Wasser der Nordsee bestätigen weitgehend die in den vorhergehenden Jahren gefundenen Ergebnisse (Fig. 1) Nach einem deutlichen Maximum im Jahre 1978 — hervorgerufen durch eine besonders starke Zufuhr im Jahre 1977 —ist die in der Nordsee insgesamt vorhandene Menge an¹³⁷Cs bis zum Jahre 1982 wieder auf rund die Hälfte zurückgegangen (Tab. 1).Auf dem Weg von den Sellafield Works an der Irischen See bis in die Nordsee ist eine starke Verschiebung des¹³⁷Cs:⁹⁰Sr Verhältnisses zugunsten des⁹⁰Sr zu beobachten.Aus dem zeitlichen Verlauf dieses Verhältnisses an verschiedenen Meßpunkten ergeben sich Transportzeiten zwischen den Sellafield Works und dem Pentland Firth von rund 3 Jahren; bis in die südöstliche Nordsee wird ein weiteres Jahr benötigt.Das Verhältnis Cs:Sr erlaubt außerdem in der südöstlichen Nordsee eine gute Unterscheidung der aus der Nordsee bzw. durch den Kanal von Süden kommenden Wassermassen, die praktisch nebeneinander her bis etwa zum Beginn des Skagerraks fließen.Die Vertikalverteilung des¹³⁷Cs zeigt, wie zu erwarten ist, jahreszeitlich bedingte Unterschiede. Es treten aber auch Effekte auf, die sich anhand der bisher vorliegenden Daten noch nicht eindeutig erklären lassen.Das in der Nordsee vorhandene⁹⁰Sr sowie das^239+240Pu zeigen ein analoges Verteilungsschema verglichen mit dem des¹³⁷Cs. Ihre Konzentrationen liegen weit unter der des¹³⁷Cs (⁹⁰Sr 17,5%,^239+240Pu 0,03%).Das Tritium zeigt bei wesentlich höheren Konzentrationen dagegen eine völlig andere Verteilung, da seine Hauptzufuhr im wesentlichen über das von Land her zufließende Süßwasser erfolgt.

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Distribution et teneur de differents radionucleides artificiels, dans les eaux de la Mer du Nord entre les années 1977 et 1981 (completes par quelques résultats de 1982 à 1984)

Résumé Les mesures de concentration du Césium 137 dans les eaux de la Mer du Nord, acquises entre les années 1977 et 1982, confirment largement les résultats obtenus au cours des années précédentes. Après un net maximum en 1978 — occassionné par un apport particulièrement fort en 1977 — la quantité totale de Césium 137 présent en Mer du Nord a régressé,jusqu'en 1982, aux alentours de la moitié de ces valeurs maximales.Il a pu être observé une modification importante du rapport Césium 137/Strontium 90, en faveur du Strontium 90, sur le trajet de Sellafield Works prés de la Mer d'Irlande jusqu'à la Mer du Nord.En suivant l'évolution temporelle de la valuer de ce rapport en différents points de mesure, on peut en déduire une durée de transport d'environ 3 ans entre Sellafield Works et Pentland Firth; une année supplémentaire est ensuite nécessaire pour pénétrer en Mer du Nord Sud-orientale.En Mer du Nord Sud-orientale, le rapport Césium/Strontium permet en outre d'effectuer une nette distinction entre les masses d'eau pénétrant respectivement par le Nord dans la Mer du Nord et celles pénétrant par le Sud et venant de la Manche. Ces masses d'eau s'écoulent pratiquement côte à côte jusqu'à l'entrée du Skagerrak.Comme l'on pouvait s'y attendre, la distribution verticale du Césium est différente suivant les saisons. Cependant il apparaît également des effects qui, sur la base des données disponibles à ce jour, ne s'expliquent pas encore clairement.Le Strontium 90 aussi bien que le Plutonium 239+240 présent dans la Mer du Nord, montrent une distribution comparable, analogue à celle du Césium 137. Leurs concentrations sont bien inférieures à celle du Césium 137 (Strontium 90 17,5%; Plutonium 239+240 0,03%).Le tritium d'autre part, — avec des concentrations significativement plus fortes —montre une distribution complètement différente, due principalement au fait qu'il est introduit par l'intermédiaire de l'écoulement d'eau douce provenant de la terre.

     

Quantitative reconstruction of the lake water paleotemperature of Daihai Lake, Inner Mongolia, China and its significance in paleoclimate

By measuring Sr/Ca ratios of the ostracod shells (Limnocthere cf. inopinata) in sediments of the Daihai Lake, and combined with Sr²⁺/Ca²⁺ ratios of the lake water, this paper obtained paleosalinity of the lake water. Vaporizing experiment of the lake water in laboratory showed that there was a quantitative relationship between salinity and oxygen isotope. Using this relationship, oxygen isotope values of the paleo-lake water were calculated. By measuring the oxygen isotope of the authigenic carbonate in the lake’s sediments, and in combination with the oxygen isotope values of the paleo-lake water, the paleotemperature of the lake water was calculated. Finally, based on these proxies, the paleoclimate in the lake basin was explored.     

基于耳石微化学的长江靖江段长颌鲚与短颌鲚生境履历重建

为了解长江靖江段两种刀鲚生态型长颌鲚与短颌鲚的生境履历的不同,利用X射线电子探针微区分析技术研究采集自长江靖江江段的长颌鲚和短颌鲚个体耳石的锶和钙微化学特征.定量分析结果显示,短颌鲚个体的耳石锶、钙比值(即Sr/Ca×10~3)稳定在2.00左右,反映了其在纯淡水生活的习性;而长颌鲚的锶、钙比值波动显著,不仅具有对应淡水生活的低值(1.18±0.48~2.11±0.94),还具有对应半咸水生活的高值(3.39±0.60~6.79±1.13),反映了其溯河洄游的生活习性.短颌鲚因在淡水生活,其淡水系数(FC)值均为1.00,2013年和2014年长颌鲚的FC值分别为0.36±0.06和0.50±0.11,证明了长颌鲚与短颌鲚群体间存在差异,而且长颌鲚不同年份群体间也并不相同.长颌鲚和短颌鲚的洄游模式存在显著差异,同时不同年份间的长颌鲚也存在生境履历差异.靖江段长颌鲚资源群可能来自不同出生地起源及生活史背景不同的群体.该江段是两类刀鲚的重要栖息地或洄游通道.     

The Interface Configuration of the Fresh‐/Dead Sea Water – Theory and Measurements

The high‐density Dead Sea water (1.235 g/cm³) forms a special interface configuration with the fresh groundwater resources of its surrounding aquifers. The fresh groundwater column beneath its surroundings is around one tenth of its length compared to oceanic water. This fact alone indicates the vulnerability of the fresh groundwater resources to the impacts of changes in the Dead Sea level and to saltwater migration. Ghyben‐Herzberg and Glover equations were used to calculate the volumes of water in coastal aquifers which were replaced by freshwater due to the interface seaward migration as a result of the drop in the level of the Dead Sea. For that purpose, the dynamic equation of Glover approach has been integrated to accommodate that type of interface readjustment. The calculated amounts of freshwater which substituted salt Dead Sea water due to the migration of interface are 3.21 · 10¹¹ m³, from a Dead Sea level of –392 m to τ411 m below sea level. The average porosity of coastal aquifers was calculated to range from 2.8 to 2.94%. Geoelectric sounding measurements showed that areas underlying the coastal aquifers formerly occupied by the Dead Sea water are gradually becoming flushed and occupied by freshwater. The latter is becoming salinized due to the residuals of Dead Sea water in the aquifer matrix, the present salinity of which is lower than that of the Dead Sea water. At the same time salt dissolution from the Lisan Marl formation is causing collapses along the shorelines in the form of sinkholes, tens of meters in diameter and depth.     

Evaluation and application of the ion microprobe in the strontium isotope geochemistry of carbonates

A modified AEI-IM20 ion microprobe has been used to measure⁸⁷Sr/⁸⁶Sr ratios in carbonates. A suite of carbonates with varying major elements (Ca, Mg, Fe, Mn) was studied at low and high (M/ΔM ? 3000) mass resolution to determine the types and intensities of molecular species isobaric with Sr peaks; Sr data collected at low mass resolution must be corrected for Ca₂ and CaMgO species. Rb/Sr ratios are extremely low, and correction for⁸⁷Rb is not required (< 0.1‰ of⁸⁷Sr).Usable Sr isotopic data may be obtained from calcite givenSr≥ 400ppm, and for Sr > 5000 ppm a precision of ～ ± 1‰ (± 0.0007) in⁸⁷Sr/⁸⁶Sr (2σ mean) can be achieved under optimum conditions. The corrections for Ca₂ and CaMgO are smaller than the within-run precision in calcite, but in dolomite the correction for CaMgO is + 1.5%. Mass fractionation corrections to⁸⁷Sr/⁸⁶Sr (based on⁸⁶Sr/⁸⁸Sr= 0.1194) are typically +8 to +10‰. Good agreement between ion probe and solid source mass spectrometer results was found for calcites of known Sr isotopic composition: ST4a (～ 400ppm Sr), average ion probe⁸⁷Sr/⁸⁶Sr= 0.7267 ± 0.0015, solid source⁸⁷Sr/⁸⁶Sr= 0.72680 ± 0.00008 [14]; JCG36 (～ 6000ppm Sr), average ion probe⁸⁷Sr/⁸⁶Sr= 0.7056 ± 0.0009, solid source⁸⁷Sr/⁸⁶Sr= 0.70588 ± 0.00009 [16]; JCG44 (～ 6000ppm Sr), average ion probe⁸⁷Sr/⁸⁶Sr= 0.7057 ± 0.0006, solid source⁸⁷Sr/⁸⁶Sr= 0.70540 ± 0.00008 [16]. The ability of the ion microprobe to measure⁸⁷Sr/⁸⁶Sr for 10-μm spots in calcite was used: (1) to measure variation in⁸⁷Sr/⁸⁶Sr of ～ 0.01 on a centimetre scale in a hydrothermally altered basalt from the Isle of Skye, northwestern Scotland; and (2) to determine the Sr isotopic composition of tiny (< 35 μm) calcite grains in a veined mantle lherzolite from Bultfontein, South Africa. Because of calcite's ubiquitous occurrence in many parageneses this technique may offer many opportunities for the measurement of fine scale heterogeneities in⁸⁷Sr/⁸⁶Sr.     

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.     

Two overlapping plates subducting beneath central Japan as revealed by strontium isotope data

In central Japan, the Pacific plate subducts westward beneath the Eurasian plate and the Philippine Sea plate subducts northwestward into the mantle wedge between the Eurasian plate and the subducted Pacific slab. There, the Northeast Japan arc is joined to the Izu-Ogasawara arc. We determined ⁸⁷Sr/⁸⁶Sr ratios and Rb and Sr contents for 47 volcanic rock samples from 15 Quaternary volcanoes in central Japan and summarized the geographical distribution of the ratios. The general trend of slowly increasing ⁸⁷Sr/⁸⁶Sr ratio from the back-arc side toward the volcanic front in the Northeast Japan arc is broken by a marked high ratio (above 0.7060) centered around Akagi volcano located at the southernmost region of the arc. Elsewhere, the ratio along the volcanic front in this arc varies within the range 0.7038 to 0.7045. The marked high ⁸⁷Sr/⁸⁶Sr ratio is considered to be due to the addition of slab-derived components transported by the Philippine Sea plate to the magma-generating region in the mantle wedge beneath central Japan. Therefore, the geographical distribution of the high ratio may correspond to that of the Philippine Sea slab-derived components in the mantle wedge and we may draw the underground outline of the Philippine Sea plate. This outline implies that an aseismic portion of the Philippine Sea plate continues a few tens km ahead of the seismic one. A belt of low ⁸⁷Sr/⁸⁶Sr ratios from the Izu Peninsula northwestward along the northern end of the Izu-Ogasawara arc coincides with the zone where the subducting Philippine Sea plate is not observed seismologically, while it is detected seismologically on both sides of the belt.     

Strontium and neodymium isotopic evidence for the heterogeneous nature and development of the mantle beneath Afar (Ethiopia)

Neodymium isotope and REE analyses of recent volcanic rocks and spinel lherzolite nodules from the Afar area are reported. The¹⁴³Nd/¹⁴⁴Nd ratios of the volcanic rocks range from 0.51286 to 0.51304, similar to the range recorded from Iceland. However, the⁸⁷Sr/⁸⁶Sr ratios display a distinctly greater range (0.70328–0.70410) than those reported from the primitive rocks of Iceland. Whole rock samples and mineral separates from the spinel lherzolite nodules exhibit uniform¹⁴³Nd/¹⁴⁴Nd ratios (ca. 0.5129) but varied⁸⁷Sr/⁸⁶Sr ratios in the range 0.70427–0.70528.The SrNd isotope variations suggest that the volcanic rocks may have been produced by mixing between two reservoirs with distinct isotopic compositions. Two possible magma reservoirs in this area are the source which produced the “MORB-type” volcanics in the Red Sea and Gulf of Aden and the anomalous source represented by the nodule suite. The isotopic composition of the volcanics is compatible with mixing between these two reservoirs.It is shown that the anomalous source with a high⁸⁷Sr/⁸⁶Sr ratio cannot have been produced by simple processes of partial melting and mixing within normal mantle. Instead the high⁸⁷Sr/⁸⁶Sr is equated with a fluid phase. A primitive cognate fluid, subducted seawater or altered oceanic lithosphere may have been responsible for the generation of the source with a high⁸⁷Sr/⁸⁶Sr ratio.     

Tracing effects of decalcification on solute sources in a shallow groundwater aquifer, NW Germany

δ⁸⁷Sr values and Ca/Sr ratios were employed to quantify solute inputs from atmospheric and lithogenic sources to a catchment in NW Germany. The aquifer consists primarily of unconsolidated Pleistocene eolian and fluviatile deposits predominated by >90% quartz sand. Accessory minerals include feldspar, glauconite, and mica, as well as disperse calcium carbonate in deeper levels. Decalcification of near-surface sediment induces groundwater pH values up to 4.4 that lead to enhanced silicate weathering. Consequently, low mineralized Ca–Na–Cl- and Ca–Cl-groundwater types are common in shallow depths, while in deeper located calcareous sediment Ca–HCO₃-type groundwater prevails. δ⁸⁷Sr values and Ca/Sr ratios of the dissolved pool range from 7.3 to −2.6 and 88 to 493, respectively. Positive δ⁸⁷Sr values and low Ca/Sr ratios indicate enhanced feldspar dissolution in shallow depths of less than 20 m below soil surface (BSS), while equilibrium with calcite governs negative δ⁸⁷Sr values and elevated Ca/Sr ratios in deep groundwater (>30 m BSS). Both positive and negative δ⁸⁷Sr values are evolved in intermediate depths (20–30 m BSS). For groundwater that is undersaturated with respect to calcite, atmospheric supplies range from 4% to 20%, while feldspar-weathering accounts for 8–26% and calcium carbonate for 62–90% of dissolved Sr²⁺. In contrast, more than 95% of Sr²⁺ is derived by calcium carbonate and less than 5% by feldspar dissolution in Ca–HCO₃-type groundwater. The surprisingly high content of carbonate-derived Sr²⁺ in groundwater of the decalcified portion of the aquifer may account for considerable contributions from Ca-containing fertilizers. Complementary tritium analyses show that equilibrium with calcite is restricted to old groundwater sources.     

Strontium stable isotopes fractionate in the soil environments?

This study shows that the stable isotopic composition of strontium (the ⁸⁸Sr/⁸⁶Sr ratio expressed as δ^88/86Sr value relative to the NBS987 standard) varies significantly in sedimentary terrestrial environments. The abundances of ⁸⁶Sr, ⁸⁸Sr isotopes were analyzed by MC-ICP-MS “Nu Plasma”. All studied rocks and waters show δ^88/86Sr values that are distinctly different from the measured NBS987 standard (yielding 0.01 ± 0.05‰, all errors are reported as 2σ). Modern corals from the northern Gulf of Aqaba, Red Sea yielded significantly different value than seawater (δ^88/86Sr = 0.22 ± 0.07‰, compared to 0.35 ± 0.06‰, respectively), in an excellent correlation with the δ^88/86Sr analyses reported by Fietzke and Eisenhauer [Fietzke, J., Eisenhauer, A., 2006. Determination of temperature-dependent stable strontium isotopes (⁸⁸Sr/⁸⁶Sr) fractionation via bracketing standard MC-ICP-MS. Geochm. Geophys. Geosyst. 7 (no. 8)] on other coral samples. All carbonate samples that originated in the marine environment: corals (porites and acropora from the northern Gulf of Aqaba); Cretaceous limestone and runoff from the Judea Mountains as well as lacustrine evaporitic aragonite (Dead Sea); and Red Sea and Atlantic seawater yield an average δ^88/86Sr value of 0.26 ± 0.1‰. On the other hand, secondary materials (products of chemical weathering) from the terrestrial environment of the Judea Mountain such as terra rossa soil and speleothem calcite (that derives its Sr from the above-lying soil) yielded significantly lower δ^88/86Sr value of − 0.17 ± 0.06‰. This indicates that strontium isotopes fractionate in the soil environment calling for a possible development of strontium isotopes as a tracer for processes of chemical weathering and pedogenesis.     

Stratigraphy and otolith microchemistry of the naked carp Gymnocypris przewalskii (Kessler) and their indication for water level of Lake Qinghai during the Ming Dynasty of China

Otoliths are biogenic carbonate minerals in the inner ear of teleost fish, whose compositions can record the physical and chemical conditions of the ambient water environment inhabited by individual fish. In this research, the fishbones and otoliths of naked carp sampled near the Bird Island, offshore Lake Qinghai, were dated and analyzed for mineralogy and microchemical compositions. Comparing the microchemical compositions of ancient otoliths with those of modern otoliths, we conclude that the ancient naked carps inhabited a relict lake formed when the lake shrank from a high lake level, by combining with the AMS-14 C ages of fishbones and otoliths, the stratigraphy and surrounding topography of the sample site. AMS-14 C dating results of ancient fishbones and otoliths show that these naked carps lived from 680 to 300 years ago, i.e. during the Ming Dynasty of China. The X-ray diffraction(XRD) patterns demonstrate that the ancient lapillus is composed of pure aragonite, identical to modern one, indicating that the mineral of lapillus didn't change after a long time burial and that the ancient lapillus is suitable for comparative analysis thereafter. Microchemical results show that both ratios of Mg/Ca((70.12±18.50)×10?5) and ? 18O((1.76±1.03)‰) of ancient lapilli are significantly higher than those of modern lapilli(average Mg/Ca=(3.11±0.41)× 10?5 and ? 18O=(?4.82±0.96)‰). This reflects that the relict water body in which the ancient naked carp lived during the Ming Dynasty was characterized by higher Mg/Ca and ? 18 O ratios than modern Lake Qinghai, resulting from strong evaporation after being isolated from the main lake, similar to today's Lake Gahai. Based upon the stratigraphy and altitude of naked carp remains, it can be inferred that the altitude of lake level of Lake Qinghai reached at least 3202 m with a lake area of 4480 km2 during the Ming Dynasty, approximately ~5% larger than it is today.     

Sr isotope evolution during chemical weathering of granites —Impact of relative weathering rates of minerals

The Sr isotopic systematics in the weathering profiles of biotite granite and granite porphyry in southern Jiangxi Province were investigated. The results showed that during the chemical weathering of granites, remarked fractionation occurred between Rb and Sr. During the early stages of chemical weathering of granites, the released Sr/Si and Sr/Ca ratios are larger than those of the parent rocks, and the leaching rate of Sr is higher than those of Si, Ca, K, Rb, etc. Dynamic variations in relative weathering rates of the main Sr-contributing minerals led to fluctuation with time in⁸⁷Sr/⁸⁶Sr ratios of inherent and released Sr in the weathering crust of granite. Successive weathering of biotite, plagioclase and K-feldspar made⁸⁷Sr/⁸⁶Sr ratios in the weathering residues show such a fluctuation trend as to decrease first, increase, and then decrease again till they maintain stable. This work further indicates that when Sr isotopes are used to trace biogeochemical processes on both the catchment and global scales, one must seriously take account of the preferential release of Sr from dissolving solid phase and the fluctuation of⁸⁷Sr/⁸⁶Sr ratios caused by the variations of relative weathering rates of Sr-contributing minerals.     

Effect of sea water interaction on strontium isotope composition of deep-sea basalts

Analyses of rim-to-interior samples of fresh tholeiitic pillow basalts, deuterically altered holocrystalline basalts, and older, weathered tholeiitic basalts from the deep sea indicate that ⁸⁷Sr/⁸⁶Sr ratios of the older basalts are raised by low temperature interaction with strontium dissolved in sea water. ⁸⁷Sr/⁸⁶Sr correlates positively with H₂O in these basalts; however, there is little detectable modification of the strontium isotope composition in rocks with H₂O contents less than 1%. The isotope changes appear to be a function of relatively long-term, low-temperature weathering, rather than high-temperature or deuteric alteration. Strontium abundance and isotopic data for these rocks suggest that strontium content is only slightly modified by interaction with sea water, and it is a relatively insensitive indicator of marine alteration. Average Rb-Sr parameters for samples of apparently unaltered basalt are: Rb= 1.11ppm; Sr= 132ppm; ⁸⁷Sr/⁸⁶Sr= 0.70247.     

Strontium and neodymium isotopic compositions of detrital sediment of NS90-103 from South China Sea: Variations and their paleoclimate implication

Strontium, neodymium isotopic compositions and trace elements of the detrital sediments of Core NS90-103 from South China Sea were analyzed. The results show that the⁸⁷Sr/⁸⁶Sr ratios of the detritus during the last glacial range from 0.722 4 to 0.723 0. They are significantly higher than those during the Holocene and the maximum of the last interglacial, which range from 0.721 0 to 0.721 7. This indicates stronger continental weathering during the last glacial. On the other hand, the¹⁴³Nd/¹⁴⁴Nd ratios of these detritus are higher during the last glacial too, similar to the variation of the⁸⁷Sr/⁸⁶Sr ratios. The trace element geochemistry of these detritus indicates that more authigenic sediments, such as ferromanganese, during the last glacial may partly contribute to the increase of¹⁴³Nd/¹⁴⁴Nd ratios. Furthermore, much more detritus from continent of South China to the north of the South China Sea may probably contribute to¹⁴³Nd/¹⁴⁴Nd ratios increase during the last glacial, which was the result of the enhancement of northeast monsoon.     

A geochemical study of island-arc and back-arc tholeiites from the Scotia Sea

⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd ratios, REE and selected minor and trace elements are presented and compared for present-day volcanic rocks in the Scotia Sea.Tholeiitic basalts from the South Sandwich Islands show widely ranging contents of some lithophile elements, e.g. K₂O (0.09–0.55%) and Rb (1.55–14.2 ppm), but fairly constant Na₂O and Sr. Total REE contents range from about 4–20 times chondritic abundances with significant light-REE depletion and both positive and negative Eu anomalies. The variations in minor and trace element abundances are consistent with low-pressure fractional crystallization of plagioclase and clinopyroxene but only minor amounts of olivine. The⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd ratios of the parental magmas are thought be 0.7038–0.7039 and 0.51301–0.51314 respectively, and indicate derivation of at least some⁸⁷Sr from subducted ocean crust.The back-arc tholeiites in the Scotia Sea have lower⁸⁷Sr/⁸⁶Sr ratios (0.7028–0.7033), similar¹⁴³Nd/¹⁴⁴Nd ratios (0.51305) and are variably light-REE-enriched(Ce_N/Yb_N= 1.0–1.6). Total REE contents are comparable to those of the South Sandwich Islands tholeiites.     

Changes in the Dead Sea Level and their Impacts on the Surrounding Groundwater Bodies

In this paper the reaction of the salt‐/freshwater interface due to the changes in the Dead Sea level are elaborated at in details by using the inflows into the Dead Sea, the outflows due to evaporation losses and artificial discharges, and the hydrographic registrations of the Dead Sea level. The analyses show that the interface seaward migration resulted in a groundwater discharge of around 423 Mio m³ per meter drop in the level of the Dead Sea in the period 1994–1998 and of around 525 Mio m³/m in the period 1930–1937. The additional amount of groundwater joining the Dead Sea due to the interface seaward migration was 51 Mio m³ per one square kilometer of shrinkage in the area of the Dead Sea in the period 1930–1937 and 91 Mio m³/km² in the period 1994–1998. The riparian states of the Dead Sea are nowadays loosing 370 Mio m³/a of freshwater to the Dead Sea through the interface readjustment mechanisms as a result of their over exploitation of waters which formerly fed the Dead Sea.     

Strontium isotope composition in volcanic rocks from the Northeast Japan arc

In the Northeast Japan arc, a number of Quaternary volcanoes form a long, narrow belt, parallel to the Japan Trench. ⁸⁷Sr/⁸⁶Sr ratios were determined in 52 specimens of volcanic rocks from 27 volcanoes in the Northeast Japan arc area. The results reveal that the ratios change systematically in space. Decreasing ⁸⁷Sr/⁸⁶Sr ratios across the arc were confirmed over a wide area of Northeast Japan. In the same direction, increases in both Rb and Sr contents were also found. The regular trends are considered to be a strong constraint for elucidation of subduction-originated magma genesis at the Eurasia plate vs. Pacific plate boundary. In the northern region of the Northeast Japan arc, ⁸⁷Sr/⁸⁶Sr ratios in volcanic rocks along the volcanic front were almost constant (0.7038–0.7045) and slightly higher than those from the Izu-Ogasawara arc (0.7032–0.7038). This suggests that “interactions” between the Eurasia plate and the Pacific plate, and those between the Philippine Sea plate and the Pacific plate are slightly different. The southern region of the Northeast Japan arc, where the direction of the volcanic front bends from southward to westward, showed anomalously high ⁸⁷Sr/⁸⁶Sr ratios, reaching to 0.7077. This region coincides with the triple junction of the Eurasia, Pacific and Philippine Sea plates, suggesting “anomalous interaction” at the triple junction.     

Controls on shell Mg/Ca and Sr/Ca in cultured planktonic foraminiferan, Globigerinoides ruber (white)

Mg/Ca and Sr/Ca ratios were determined on a single species of planktonic foraminiferan, Globigerinoides ruber (white), collected from the Gulf of Eilat and cultured in seawater at five different salinities (32 to 44), five temperatures (18 to 30 °C) and four pH values (7.9 to 8.4). The Mg/Ca-temperature calibration of cultured G. ruber (with an exponential slope of 8 ± 3%/°C) agrees well with previously published calibrations from core-tops and sediment traps. However, the dependence of Mg/Ca on salinity (with an exponential slope of 5 ± 3%/psu) is also significant and should be included in the calibration equation. With this purpose, we calculated a calibration equation for G. ruber dependent on both temperature and salinity within the 95% confidence limits:

Mg/Ca(mmol/mol)=exp[0.06(±0.02)*S(psu)+0.08(±0.02)*T(°C)−2.8(±1.0)],R²=0.95