Sr-Nd isotopic compositions of the Changjiang sediments: Implications for tracing sediment sources

The suspended particulate and fine-grained floodplain sediments were collected from the main stream and tributaries of the Changjiang River for Sr-Nd isotopic measurements. The εNd(0) values gradually decrease downstream from -10.8 on average in the upper reaches to -12.3 in the lower reaches, whereas the 87Sr/86Sr ratios increase correspondingly, averaging 0.721899 and 0.725826 respectively in the upper and middle-lower reaches. The compositional variations primarily reflect the complex con- trols of provenance rocks, chemical weathering, and sediment characters between different catchments, among which the abnormal Sr-Nd isotopic compositions of the Yalong, Fujiang, Tuojiang and Yuanjiang rivers indicate the sediment provenance contributions from the Emeishan Basalt in the upper reaches and the old metamorphic and siliceous rocks in the middle-lower reaches. The Sr-Nd isotopic ratios of the Changjiang sediments can better reflect the average composition of weathered continental crust compared to other major rivers in the world because of the unique source rock types in the Changjiang drainage basin. The recognition of the Sr-Nd isotopic systematics of the Changjiang sediments will contribute to our understanding of the Changjiang evolution history and continental weathering processes during the Cenozoic, and also to reconstructing the paleoenvironmental changes in East China and the marginal seas.     

Uranium and thorium isotopes in the rivers of the Amazonian basin: hydrology and weathering processes

Two expeditions (October 1989 and May 1992) were carried out to two points of the main Amazon River channel and four tributaries. The Solimões and Madeira rivers, taking their origin in the Andes, are whitewater rivers. The Negro River is a typical acid, blackwater river. The Trombetas River flows through bauxite‐rich areas, and is characterized by low concentrations of dissolved humic substances. The ²³⁸U, ²³⁴U, ²³²Th and ²³⁰Th activities were recorded from dissolved, suspended particulate phases and river bank sediments. The latter were analysed for their ²²⁶Ra, ²²⁸Ra and ²¹⁰Pb contents, and also subjected to leaching with 0·2 M hydroxylamine–hydrochloride solution to determine the concentrations of radionuclides bound to amorphous Fe hydroxides and Mn oxides and hydroxides. The dissolved U average concentration in the Amazon system is ten times lower than the mean world river concentration. The uranium concentration observed at Óbidos in the lower Amazon (0·095 µg L^?1), where the U content in the river bank sediments and suspended matter is lowest, suggests U release from the solid phase during river transport. About 485 t of U are transported annually to the Amazon delta area in dissolved form, and 1943 t bound to suspended particulate matter. Total U and Th concentrations in the river bank sediments ranged from 1·59 to 7·14 µg g^?1 and from 6·74 to 32 µg g^?1, respectively. The highest concentrations were observed in the Trombetas River. The proportion extracted by means of the hydroxylamine solution (HL) was relatively high for U in the Trombetas river bank sediment (31%) and for Th in the Solimões sediment (30%). According to the alpha recoil effects, the ²³⁴U/²³⁸U activity ratios of the Andean river waters and downstream Amazon water (Óbidos) were >1, but were <1 in the Negro River (at Manaus). The activity ratios of dissolved U correlate with pH and also with the U activity ratios in the river bank sediment hydroxylamine extracts. As expected, the ²³⁴U/²³⁸U activity ratios in river bank sediments were <1 in the Andean rivers and in the downstream Amazon, but they were >1 in the Trombetas and Negro rivers. Such ratios probably result from the binding of dissolved uranium to solid sediment. The ²²⁸Th/²³²Th ratios of river bank sediments were close to unity (except for the Negro River, where it is lower), suggesting no significant Th exchanges between the river water and the sediment. The ²²⁶Ra/²³²Th activity ratios were <1, and the ²²⁶Ra/²²⁸Ra activity ratios generally were significantly higher than the activity ratios of their respective parents. This perhaps is the result of easier leaching of the ²²⁶Ra parent, ²³⁰Th, from solid material (owing to the alpha recoil effect) than of the ²²⁸Ra parent. Uranium and thorium isotopes were used as tools to evaluate the chemical weathering rate of rocks in the Amazon system, which was estimated to be 2·7 cm 1000 year^?1 s^?1. Copyright © 2002 John Wiley & Sons, Ltd.     

Pb, Nd, and Sr isotopic constraints on the origin of Miocene basaltic rocks from northeast Hokkaido, Japan: Implications for opening of the Kurile back-arc basin

Late Miocene (7–9 Ma) basaltic rocks from the Monbetsu‐Kamishihoro graben in northeast Hokkaido have chemical affinities to certain back‐arc basin basalts (referred to herein as Hokkaido BABB). Pb‐, Nd‐ and Sr‐isotopic compositions of the Hokkaido BABB and arc‐type volcanic rocks (11–13 Ma and 4–4.5 Ma) from the nearby region indicate mixing between the depleted mantle and an EM II‐like enriched component (e.g. subducted pelagic sediment) in the magma generation. At a given ⁸⁷Sr/⁸⁶Sr, Hokkaido BABB have slightly lower ¹⁴³Nd/¹⁴⁴Nd and slightly less radiogenic ²⁰⁶Pb/²⁰⁴Pb compared with associated arc‐type lavas, but both these suites are difficult to distinguish solely on the basis of isotopic compositions. These isotopic data indicate that while generation of the Hokkaido BABB involves smaller amounts of the EM II‐like enriched component than do associated arc lavas, Hokkaido BABB are isotopically distinct from basalts produced at normal back‐arc basin spreading centers. Instead, northeast Hokkaido BABB are more similar to basalts erupted during the initial rifting stage of back‐arc basins. The Monbetsu‐Kamishihoro graben may have developed in association with extension that formed the Kurile Basin, suggesting that opening of the basin continued until late Miocene (7–9 Ma).     

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.     

Measuring and modeling vertical gradients in suspended sediments in the Solimões/Amazon River

Accurately measuring sediment flux in large rivers remains a challenge due to the spatial and temporal cross‐sectional variability of suspended sediment concentrations in conjunction with sampling procedures that fail to accurately quantify these differences. This study presents a field campaign methodology that can be used to improve the measurement of suspended sediment concentrations in the Amazon River or similarly large rivers. The turbidity signal and Rouse model are together used in this study to define the spatial distribution of suspended sediment concentrations in a river cross‐section, taking into account the different size fractions of the sediment. With this methodology, suspended sediment fluxes corresponding to each sediment class are defined with less uncertainty than with manual samples. This paper presents an application of this methodology during a field campaign at different gauging stations along a 3,000‐km stretch of the Solimões/Amazon River during low water and flood periods. Vertical concentration profiles and Rouse model applications for distinctive sediment sizes are explored to determine concentration gradients throughout a cross‐section of the river. The results show that coupling both turbidity technology and the Rouse model may improve our understanding of the spatial distribution of different sediments fractions sizes in the Solimões/Amazon River. These data are very useful in defining a pertinent monitoring strategy for suspended sediment concentrations in the challenging context of large rivers.     

Oxygen isotopic compositions of Central Andean plutonic and volcanic rocks,latitudes 26°–29° south

Oxygen isotope data are reported for 27 igneous rocks of Mesozoic to Quaternary age from the Central Andes. 26–29°S. The plutonic rocks, and most of the volcanics, have δ¹⁸O values between 6.2 and 8.3‰.The whole-rock δ¹⁸O values show a weak correlation with initial⁸⁷Sr/⁸⁶Sr data. This O-Sr array differs from documented trends for calc-alkaline plutonic suites from California, Scotland and northern Italy, but overlaps with data for volcanic and plutonic rocks from Ecuador, northern Chile and southern Perú.The oxygen isotope results indicate that the magmas evolved without significant contamination from supracrustal rocks (e.g., rocks that experienced¹⁸O enrichment during surficial weathering). The available O, Sr and Pb isotopic data for these rocks are best explained by magma generation in the upper mantle or lower crust. From the Late Mesozoic on, the⁸⁷Sr/⁸⁶Sr values were modified at depth by isotopic exchange between the magma and a continually thickening crust of plutonic rocks of Late Precambrian to early Mesozoic age.     

紫坪铺水库沉积物Sr同位素及元素组成变化对2008年汶川大地震的响应

2008年5月12日里氏7.9级汶川大地震引发了超过56000多个山体滑坡,在龙门山地区产生巨量的碎屑物质,极大地影响了流域的地表过程.然而,地震对河流碎屑物质组成及沉积过程的改变却知之甚少.紫坪铺水库超高沉积速率（平均74 cm/a）的沉积物完整记录了汶川地震前后的沉积过程,为研究2008年汶川地震对流域地表物质搬运及沉积物组成的影响提供了宝贵的素材.本研究测试了汶川地震前后紫坪铺水库沉积物的Sr同位素以及元素组成,结果表明其在地震之后均发生了显著变化.震后沉积物⁸⁷Sr/⁸⁶Sr与Rb/Sr比值同步降低,并且和沉积物化学蚀变指数（CIA）呈正相关性,反映了地震滑坡导致的新鲜物质对沉积物的贡献,特别是地震后强径流的2010—2011年.地震前后沉积物组成的差异性,为利用沉积物反演水文气候和构造事件及其环境效应提供了基础和潜在指标.     

Late Cenozoic alkaline volcanism in the northwestern Caribbean: tectonic setting and Sr isotopic characteristics

A province of alkaline volcanism has developed over the last 10 m.y. in the northwestern part of the Caribbean plate. Most of the volcanism is Quaternary in age and follows an apparent halving of the spreading rate at the Cayman Rise spreading center 2.4 m.y. ago. Intraplate deformation in Central America and the Nicaraguan Rise has produced a series of north-south orientated grabens. This extensional tectonism is associated temporally and spatially with some of the alkaline magmatism. Strontium isotopic ratios of rocks from sixteen of these centers of volcanism enable three separate areas with different isotopic characteristics to be identified. The largest area corresponds to the Nicaraguan Rise and is characterized by low⁸⁷Sr/⁸⁶Sr ratios (0.7026–0.7031). A more concentrated area of alkaline magmatism in northeastern Costa Rica has intermediate⁸⁷Sr/⁸⁶Sr ratios (0.7036–0.7038) which are within the range shown by the adjacent calc-alkaline volcanoes. In central Hispaniola high⁸⁷Sr/⁸⁶Sr ratios (0.7047–0.7063) are found in strongly alkalic rocks and in rocks that are transitional to calc-alkaline in nature. In both Costa Rica and Hispaniola the increased radiogenic strontium may have come from volatile-rich fluids escaping from adjacent subducting slabs of oceanic crust. The isotopic differences between the two areas may be related to the relative longevity and high rate of subduction in Costa Rica compared to Hispaniola. The Costa Rican alkaline rocks overlie a segment of the Cocos plate which is being subducted at a smaller angle (～ 35°) than at the rest of the Central American arc.     

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.     

Geochemical and Sr–Nd–Pb isotopic investigation of Triassic granitoids and basement rocks in the northern Gyeongsang Basin, Korea: Implications for the young basement in the East Asian continental margin

Abstract We present chemical and Sr–Nd–Pb isotopic compositions of three Triassic (226–241 Ma) calc‐alkaline granitoids (the Yeongdeok granite, Yeonghae diorite and Cheongsong granodiorite) and basement rocks in the northern Gyeongsang basin, south‐eastern Korea. These plutons exhibit typical geochemical characteristics of I‐type granitoids generated in a continental magmatic arc. The Yeongdeok and Yeonghae plutons have similar initial Sr, Nd and Pb isotope ratios (⁸⁷Sr/⁸⁶Sr_initial = 0.7041 ~ 0.7050, ?_Nd(t) = 2.3 ~ 4.0, ²⁰⁶Pb/²⁰⁴Pb_feldspar = 18.22 ~ 18.34), but distinct rare earth element patterns, suggesting that the two plutons formed from partial melting of a similar source material at different depths. The Cheongsong pluton has slightly more enriched Sr–Nd–Pb isotopic compositions (⁸⁷Sr/⁸⁶Sr_initial = 0.7047 ~ 0.7065, ?_Nd(t) = 3.9 ~ 2.8, ²⁰⁶Pb/²⁰⁴Pb_feldspar = 18.24 ~ 18.37) than the other two plutons. The Nd model ages of the basement rocks (1.1 ~ 1.4 Ga) are slightly older than those of the plutons (0.6 ~ 1.0 Ga). The initial Sr and Nd isotopic ratios of the plutons can be modeled by the mixing between the mid‐oceanic ridge basalt‐like depleted mantle component and the crustal component represented by basement rocks, which is also supported by Pb isotope data. The Sr and Nd isotope data from granitoids and basement rocks suggest that the Gyeongsang basin, the Hida belt and the inner zone of south‐western Japan share relatively young basement histories (middle Proterozoic), compared with those (early Proterozoic to Archean) of the Gyeonggi and Yeongnam massifs and the Okcheon belt. The Nd isotope data of basement rocks suggest that the Hida belt might be better correlated with the basement of the Gyeongsang basin than the Gyeonggi massif, the Okcheon belt or the Yeongnam massif, although it may represent an older continental margin of East Asia than the Gyeongsang basin considering its slightly older Nd model ages.     

Possible origin of K-rich volcanic rocks from Virunga,East Africa,by metasomatism of continental crustal material: Pb,Nd and Sr isotopic evidence

The isotopic compositions of Sr, Nd and Pb together with the abundances of Rb, Sr, U and Pb have been determined for mafic and felsic potassic alkaline rocks from the young Virunga volcanic field in the western branch of the East African rift system.⁸⁷Sr/⁸⁶Sr varies from 0.7055 to 0.7082 in the mafic rocks and from 0.7073 to 0.7103 in the felsic rocks. The latter all come from one volcano, Sabinyo. Sabinyo rocks have negative ε_Ndvalues ofε_Nd = ?10. Nd and Sr isotopic variations in the basic potassic rocks are correlated and plot between Sabinyo and previously reported [1] compositions (ε_Nd = +2.5;⁸⁷Sr/⁸⁶Sr≈ 0.7047) for Nyiragongo nephelinites. The Pb isotopic compositions for Sabinyo rocks are nearly uniform and average²⁰⁶Pb/²⁰⁴Pb≈ 19.4,²⁰⁷Pb/²⁰⁴Pb= 15.79–15.84,²⁰⁸Pb/²⁰⁴Pb≈ 41.2. The basic potassic rocks have similar²⁰⁶Pb/²⁰⁴Pb values but range in²⁰⁷Pb/²⁰⁴Pb and²⁰⁸Pb/²⁰⁴Pb from the Sabinyo values to less radiogenic compositions.Excellent correlations of⁸⁷Sr/⁸⁶Sr with Rb/Sr, 1/Sr and²⁰⁷Pb/²⁰⁶Pb for Sabinyo rocks suggest these to be members of a hybrid magma series. However, the nearly uniform Pb compositions for this series points to radiogenic growth of⁸⁷Sr in the magma source region following an event which homogenized the isotopic compositions but not Rb/Sr. The Rb-Sr age derived from the erupted Sabinyo isochron-mixing line is consistent with the ～500 Myr Pb-Pb age from Nyiragongo [1], which suggests that this event affected all Virunga magma sources. The event can again be traced in the Pb-Pb, Pb-Sr and Nd-Sr isotopic correlations for all Virunga rocks, including Nyiragongo, when allowances are made for radiogenic growth subsequent to this mixing or incomplete homogenization event. Inferred parent/daughter element fractionations point to a metasomatic event during which a mantle fluid invaded two lithospheric reservoirs: a +ε_Nd reservoir sampled by the Nyiragongo nephelinites and suggested to be the subcontinental mantle and a ?ε_Nd reservoir sampled by the mafic and felsic potasssic volcanism. Whether this ?ε_Nd reservoir is the crust, continental crustal material in the mantle or anomalous mantle cannot be decided from the data. The simplest answer, that this reservoir is the continental crust, seems to be at variance with experimental evidence suggesting a subcrustal origin for basic potassic magmas. Partial melting of the ancient metasomatised lithospheric domains and ensuing volcanism seems to be entirely a response to decompression and rising geotherms during rifting and thinning of the lithosphere.     

Oxygen isotopes and the origin of high-87Sr/86Sr andesites

Andesites from the Peruvian Andes and the Banda arc of Indonesia are characterized by unusually high and variable ⁸⁷Sr/⁸⁶Sr ratios. The Banda arc samples, including two cordierite-bearing lavas from Ambon, show a clear positive correlation between ⁸⁷Sr/⁸⁶Sr and δ¹⁸O. The andesitic rocks have δ¹⁸O values that range from 5.6 to 9.2‰. Over that range in δ¹⁸O, ⁸⁷Sr/⁸⁶Sr increases from 0.7044 to 0.7095. The cordierite-bearing lavas have δ¹⁸O values of approximately 15‰ and ⁸⁷Sr/⁸⁶Sr ratios of approximately 0.717. The similarity between δ¹⁸O values and ⁸⁷Sr/⁸⁶Sr ratios in total rocks and separated plagioclase phenocrysts of the Banda arc samples indicates that the measured isotope ratios are primary and have not been affected by secondary, low-temperature post-eruptive alteration. The observed variation between O and Sr isotopic ratios can be modeled by two-component mixing in which one component is of mantle isotopic composition. As the crust beneath the Banda arc is probably oceanic, contamination of the manle component may have resulted from the subduction of either continentally-derived sediments or continental crust. Mixing calculations indicate that the contaminant could have an isotopic composition similar to that observed in the cordierite-bearing lavas.The Andean samples, despite petrographic evidence of freshness, exhibit whole-rock δ¹⁸O values significantly higher than those of corresponding plagioclase phenocryst separates, indicating extensive low-temperature post-eruptive alteration. The plagioclase mineral separates show a range of δ¹⁸O values between 6.9 and 7.9‰. The ⁸⁷Sr/⁸⁶Sr ratios of these same samples are, in most instances, not significantly different from those measured for the whole rock, thus signifying that the phenocrysts and groundmass were in isotopic equilibrium at the time of eruption. Unlike the lavas of the Banda arc, the Andean lavas show no strong positive correlation between ⁸⁷Sr/⁸⁶Sr ratios and δ¹⁸O values, but instead lower ⁸⁷Sr/⁸⁶Sr ratios appear to be associated with higher δ¹⁸O values. The δ¹⁸O and ⁸⁷Sr/⁸⁶Sr values of the Peruvian samples are both slightly higher than those of “normal” island arc volcanics.The small proportions of contaminant implied by the O isotope results seem to preclude continental crustal contamination as a primary cause of high ⁸⁷Sr/⁸⁶Sr ratios. The most plausible process that can explain both O and Sr isotope results is one in which sediments of continental origin are partially melted in the subduction zone. These melts rise into overlying mantle material and subsequently participate in the formation of calc-alkaline magmas.If the involvement of a sialic component in the genesis of andesitic magma occurs in the subduction zone, melting of that sialic material signifies temperatures of at least 750–800°C at the top of the subducted lithospheric slab at depths of approximately 150 km. The fact that contamination has apparently occurred in the Banda arc samples without producing any simple widespread correlations between Sr and O isotopic compositions on the one hand and major or trace element abundances on the other, shows that isotopic correlations, possibly including pseudo-isochrons, can be produced by mixing without producing trace element mixing correlations. Because O versus Sr isotope correlations are little affected by processes of partial melting of differentiation, they provide a direct means of testing whether Sr isotopic variations in volcanic rocks are of mantle origin or are due instead to mixing with sialic material.     

“Mantle” Rb/Sr and 87Sr/86Sr ratios for clinopyroxenes from Norwegian garnet peridotites and pyroxenites

Clinopyroxenes separated from garnetiferous ultramafic rocks in the core zone of the Norwegian Caledonides have rubidium concentrations of 0.008 to 0.064 ppm, strontium concentrations of 23.5 to 421 ppm, and ⁸⁷Sr/⁸⁶Sr ratios of 0.7011 to 0.7029. The very low Rb/Sr ratios of the clinopyroxenes (less than 0.0004) suggest that their ⁸⁷Sr/⁸⁶Sr values have not varied significantly over geologic time and may approximate the initial ⁸⁷Sr/⁸⁶Sr of the eclogite-facies ultramafic mineral assemblages at their time of formation. The ultramafic rocks occur in a basement complex that yields Rb-Sr whole-rock and U-Pb zircon ages of about 1800 m.y. Garnetiferous ultramafic rocks are apparently lacking in younger (Sveconorwegian or Caledonian) sialic sequences, raising the possibility that the eclogite-facies metamorphism may have occurred at least 1800 m.y. ago. The Rb/Sr and ⁸⁷Sr/⁸⁶Sr ratios of the clinopyroxenes are as predicted for the ancient upper mantle under most evolutionary models. However, the data do not preclude the possibility that the eclogite-facies metamorphism occurred in the crust. The garnetiferous ultramafic rocks are generally enclosed by large volumes of dunite which could have shielded the eclogite-facies assemblages from contamination by fluids from the country rock during metamorphism.     

Sediment budget of the Napo River,Amazon basin,Ecuador and Peru

The upstream‐downstream sediment budget along the Napo River (100 520 km², 6300 m³ s^?1) was studied in the Andean foothills of Ecuador, at the west of the Amazon basin. A comparative study was made during four hydrological cycles (2001–2005) for three hydrological stations located upstream, and during one hydrological cycle (2004–2005) for the fourth one located near the mouth of the Napo River (region of Iquitos in Peru). This analysis showed an unusual increase in the concentration of suspended sediment recorded for the western part of the Amazon plain. Like the runoff (81 l s^?1 km²), which is a world's maximum, the erosion rate (1160 t km^?2 year^?1, i.e. 47% of total suspended solid (TSS) export at the exit of Ecuador), one of the highest for a floodplain basin is the result of a stepper slope than in the rest of the Andean foothills, where typically sedimentation phenomena are predominant, and can be explained in part by a greater tectonic activity. Similar phenomenes were evidenced in small mountainous rivers in New Guinea (Milliman and Syvitski, 1992; Milliman, 1995). On the headwaters of the Napo River drainage basin, the tectonic uplift causes the Pastaza Megafan's existence. This progressively diverts the course of Napo River towards north and also provokes the remobilization of fine fluvial deposits. Moreover, this geodynamic trend is completed by the impact of volcanic eruption, earthquakes and landslides. The combination of these phenomena, so common in the region, has provided a large sediment transfer, not only at present but also in the past, as can be confirmed by the presence of incised terraces, mainly formed by volcanic materials. Then, these results were compared with a similar study carried out further south in the Madeira basin at the Bolivian foothills. These studies show the spatio‐temporal variability of the relation between sediment transfer and geodynamic processes at the Andean Piedmont. Copyright © 2009 John Wiley & Sons, Ltd.     

Sr–Nd isotope ratios of gabbroic and dioritic rocks in a Cretaceous-Paleogene granite terrain, Southwest Japan

Abstract Whole‐rock chemical and Sr and Nd isotope data are presented for gabbroic and dioritic rocks from a Cretaceous‐Paleogene granitic terrain in Southwest Japan. Age data indicate that they were emplaced in the late Cretaceous during the early stages of a voluminous intermediate‐felsic magmatic episode in Southwest Japan. Although these gabbroic and dioritic rocks have similar major and trace element chemistry, they show regional variations in terms of initial Sr and Nd isotope ratios. Samples from the South Zone have high initial ⁸⁷Sr/⁸⁶Sr (0.7063–0.7076) and low initial Nd isotope ratios (?_Nd, ?2.5 to ?5.3); whereas those from the North Zone have lower initial ⁸⁷Sr/⁸⁶Sr (usually less than 0.7060) and higher Nd isotope ratios (?_Nd, ?0.8 to + 3.3). Regional variations in Sr and Nd isotope ratios are similar to those observed in granitic rocks, although gabbroic and dioritic rocks tend to have slightly lower Sr and higher Nd isotope ratios than granitic rocks in the respective zones. Limited variations in Sr and Nd isotope ratios among samples from individual zones may be attributed partly to a combination of upper crustal contamination and heterogeneity of the magma source. Contamination of magmas by upper crustal material cannot, however, explain the observed Sr and Nd isotope variations between samples from the North and South Zones. Between‐zone variations would reflect geochemical difference in magma sources. The gabbroic and dioritic rocks are enriched in large ion lithophile elements (LILE) and depleted in high field strength elements (HFSE), showing similar normal‐type mid‐ocean ridge basalt (N‐MORB) normalized patterns to arc magmas. Geochronological and isotopic data may suggest that some gabbroic and dioritic rocks are genetically related to high magnesian andesite. Alternatively, mantle‐derived mafic or intermediate rocks which were underplated beneath the crust may be also plausible sources for gabbroic and dioritic rocks. The magma sources (the mantle wedge and lower crust) were isotopically more enriched beneath the South Zone than the North Zone during the Cretaceous‐Paleogene. Sr and Nd isotope ratios of the lower crustal source of the granitic rocks was isotopically affected by mantle‐derived magmas, resulting in similar initial Sr and Nd isotope ratios for gabbroic, dioritic and granitic rocks in each zone.     

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.     

Isotopic evidence for local derivation of strontium in deep-seated, fracture-filling calcite from granitic rocks in drill hole GT-2, Los Alamos scientific laboratory dry hot rock program

Fracture-filling calcites from GT-2 Drill Core (LASL-DHR Program) yield ⁸⁷Sr/⁸⁶Sr ranging from 0.724 to 0.734. These data indicate derivation of Sr in the calcite from 1.7 ± 0.1 b.y. old granitic basement rocks at depth and not from the overlying Madera Formation (Pennsylvanian) which possesses high Sr content with ⁸⁷Sr/⁸⁶Sr near 0.709. This, in turn, indicates that meteoric waters did not transport significant amounts of Sr from the Madera Formation into the Precambrian basement rocks to great depth.     

Big difference in ~(87)Sr/ ~(86)Sr ratios of basalt and basin water: higher ~(87)Sr/ ~(86)Sr ratios in plagioclase

We analyzed the ~(87)Sr/~(86)Sr ratios of basaltic rocks and basin water in Xuyi,China,and found a big difference,which may challenge conventional wisdom on the contribution of basalt weathering in end-member analysis.Results of an in-house weathering experiment suggest that rainwater and dust are not responsible for the difference.By isolating the major minerals in basalt,we found that plagioclase has much higher ~(87)Sr/~(86)Sr ratios than bulk basalt and basin water,which might explain the difference in ~(87)Sr/~(86)Sr ratios of basalt and basin water.We inferthatlow-temperaturehydrothermalalteration increased the ~(87)Sr/~(86)Sr ratios of plagioclase.Future analyses of end-member contribution in a mixed-rock basin should take into account that basin water and plagioclase have higher ~(87)Sr/~(86)Sr ratios than basaltic rocks.     

Geochronology of Ailaoshan-Jinshajiang alkalirich intrusive rocks and their Sr and Nd isotopic characteristics

Twenty-nine isotopic ages, ranging from 41 to 27 Ma, are presented for the alkali-rich intrusive rocks and their coexisting alkaline volcanic rocks, lamprophyres and acidic porphyries, indicating that they are Tertiary in age. The alkali-rich intrusive rocks have¹⁴³Nd/¹⁴⁴Nd ratios from 0. 512 415 to 0. 512 544, and⁸⁷Sr/⁸⁶Sr ratios from 0.705 4 to 0.706 8, suggesting that their material originates from an enriched mantle source. Project supported by the National Natural Science Foundation of China and the Special Grant of the President of Chinese Academy of Sciences.     

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.