A Sm-Nd isotopic study of atmospheric dusts and particulates from major river systems

¹⁴³Nd/¹⁴⁴Nd ratios, and Sm and Nd abundances, are reported for particulates from major and minor rivers of the Earth, continental sediments, and aeolian dusts collected over the Atlantic, Pacific, and Indian Oceans. Overall, Sm/Nd ratios and Nd isotopic compositions in contemporary continental erosion products vary within the small ranges of ¹⁴⁷Sm/¹⁴⁴Nd= 0.115 ± 0.01 and¹⁴³Nd/¹⁴⁴Nd= 0.51204 ± 0.0002 (ε_Nd = −11.4 ± 4). The average period of residence in the continental crust is estimated to be1.70 ± 0.35Ga.

These results combined with data from the literature have implications for the age, history, and composition of the sedimentary mass and the continental crust: (1) The average “crustal residence age” of the whole sedimentary mass is about 1.9 Ga. (2) The range of Nd isotope compositions in the continent derived particulate input to the oceans is the same as Atlantic sediments and seawater, but lower than those of the Pacific, demonstrating the importance of Pacific volcanism to Pacific Nd chemistry. (3) The average ratio of Sm/Nd is about 0.19 in the upper continental crust, and has remained so since the early Archean. This precludes the likelihood of major mafic to felsic or felsic to mafic trends in the overall composition of the upper continental crust through Earth history. (4) Sediments appear to be formed primarily by erosion of continental crust having similar Sm/Nd ratios, rather than by mixing of mafic and felsic compositions. (5) The average ratio of ¹⁴³Nd/¹⁴⁴Nd≈ 0.5117 (ε_Nd ≈ −17) in the upper continental crust, assuming its mean age is about 2 Ga. (6) The uniformity of the SmNd isotopic systematics in river and aeolian particulates primarily reflects efficient recycling of old sediment by sedimentary processes on a short time scale compared to the amount of time the material has resided in the crust.     

Shape analysis of Pacific seamounts

Shape statistics have been compiled from 85 profiles of well-surveyed Pacific seamounts in the height range 140–3800 m. A flat-topped cone was fit to each seamount's cross-sectional profile maintaining the slopes of the sides as closely as possible. On each profile a basal widthd_b, a summit widthd_t, and a maximum heighth, were measured. The height-to-basal-radius ratio isξ_h is estimated by the ratio2hd_b and flatnessf by the ratiod_td_b. Slope angleφ = arctan(ε) is estimated fromε =2h(d_b − d_t). Summit height and basal radius are found to be highly correlated (r = 0.93). The 85-point sample mean of the height-to-basal-radius ratio isξ_h = 0.21 ± 0.08 implying that a seamount's summit height is typically one fifth its basal radius. Despite the high correlation, individual points show some scatter, and there may be groupings into different morphological types. For example, all but one of the seamounts with summit heights above 1000 m have values ofξ_h that are larger than the sample mean. The 85-point sample mean of flatness isf = 0.31 ± 0.18. Data points show a large scatter with values off varying between 0 (a pointy cone) and 0.69 (a flat-topped cone). A histogram representation of flatness, however, indicates that certain values off may be more common than others: the histogram shows a bimodal distribution with maxima occurring at values off in the ranges 0.10–0.20 and 0.35–0.50. Moreover, there is some evidence that the mean flatness decreases with summit height so that the preferred shape of a large-sized seamount may be a pointy cone. Slope angle has an 85-point sample mean ofφ = 18 ± 6°; individual values ofφ vary between 5° and 36°. In addition to having a lower than average mean flatness seamounts with heights above 2600 m also have a lower than average mean slope angle (15°). To determine which variables account for most of the observed variation in the seamount shapes, a multivariate principal component analysis was performed on the data using five shape variables (summit height, basal radius, summit radius, flatness, and slope). The analysis indicates that most of the variation is described by two variables: flatness and summit height.     

Age and isotope geochemistry of the Archaean Pongola and Usushwana suites in Swaziland, southern Africa: a case for crustal contamination of mantle-derived magma

The igneous rocks of the Pongola Supergroup (PS) and Usushwana Intrusive Suite (UIS) represent a case of late Archaean continental magmatism in the southeastern part of the Kaapvaal craton of South Africa and Swaziland.

U-Pb dating on zircons from felsic volcanic rocks of the PS yields a concordia intercept age of 2940 ± 22Ma that is consistent with a Sm-Nd whole rock age of 2934 ± 114Ma determined on the PS basalt-rhyolite suite. The initial ε_Nd of−2.6 ± 0.9 is the lowest value so far reported for Archaean mantle-derived rocks. Rb-Sr whole rock dating of the PS yields a younger isochron age of 2883 ± 69Ma, which is not significantly different form the accepted U-Pb zircon age.

An internal (cpx-opx-plag-whole rock) isochron for a pyroxenite from the younger UIS yields an age of 2871 ± 30 Ma and initial ¹⁴³Nd/¹⁴⁴Nd that lies off the CHUR growth curve by ε_Nd −2.9 ± 0.2. However, Sm-Nd whole-rock data for the UIS yield an excessively high age of 3.1 Ga that conflicts with firm geological evidence showing the UIS to be intrusive into the PS.

The negative deviations of initialε_Nd from the chondritic Nd evolution curve suggest significant contamination of the PS and UIS melts by older continental crust. A mixing process with continental crust after magma segregation is supported by a high initial ⁸⁷Sr/⁸⁶Sr ratio of0.703024 ± 24 for a clinopyroxene sample from a UIS pyroxenite, compared with an expected value of 0.701 for the 2.9 Ga mantle. We therefore interpret the linear array of data points for the UIS gabbros as a mixing line between 2.87 Ga old magma and older continental crust.

Parallel LREE-enriched REE patterns, negative Nb-Ti anomalies, a distinctive and uniform ratio of Ti/Zr 46 and a narrow span of initial Nd indicate a common source for both the PS and UIS suites which is different from primitive mantle.     

A new approach to the Nd residence time in the ocean: the role of atmospheric inputs

Concentrations of rare earth elements (REE) and Nd isotopic ratios were analyzed for seawater, filtered suspension and sediment trap samples collected in the tropical Atlantic Ocean (EUMELI program, EUtrophic, MEsotrophic and oLIgotrophic sites, 20°N, 18°–21°W). This is the first REE/Nd dataset on solution and different-sized particles collected at the same site. We present direct evidence of the Nd isotopic exchange between particulate lithogenic fraction and seawater without significant mass transfer. This exchange is probably one of the main factors that simultaneously constrains the Nd concentration and isotopic ratio budget. We propose a new approach to estimate the residence time of Nd in the ocean (τ_Nd) based on isotopic exchange: 200 yr < τ_Nd< 1000 yr. The exchange requires a partial dissolution of lithogenic Nd. We estimate that the fraction of soluble Nd proportion in atmospheric dust is of the order of 20% based on the isotopic ratios. We suggest that the partial dissolution of atmospheric fallout is probably one of the main REE sources of the ocean.     

A Nd isotope investigation of sediments related to crustal development in the British Isles

The times of original fractionation of the Sm and Nd component of clastic sediments from a mantle source (≡ crustal residence age) have been estimated from Sm-Nd model ages calculated relative to a depleted mantle evolution. In this way the provenance and evolution of selected Precambrian and Phanerozoic sediments and metasediments from the British Isles have been examined. Whereas some Archaean and early Proterozoic sediments have Sm-Nd model ages that are close to their stratigraphic age, the Phanerozoic sediments analysed have model ages as much as 2.0 Ga in excess of their stratigraphic age.A more detailed study of Lower Palaeozoic sediments deposited on the northern margin of the Iapetus Ocean provides evidence for a marked change of provenance in the Ordovician after the deposition of the Dalradian Supergroup. A component with comparatively high¹⁴³Nd/¹⁴⁴Nd and Sm/Nd ratio (presumably basaltic) is present in the sediments throughout the accretionary prism. Crustal residence age estimates average about 1.5 Ga for both these Lower Palaeozoic sediments, and modern pelagic clays, and collectively fail to provide any evidence for significant continental growth during the Phanerozoic.     

Nd and Sr isotopic variations of Early Paleozoic oceans

We report¹⁴³Nd/¹⁴⁴Nd and⁸⁷Sr/⁸⁶Sr isotopic data for Lower Paleozoic phosphatic brachiopod and conodont fossils. The data appear to represent the isotopic values of Early Paleozoic seawaters. We show that different paleoceanic water masses can be distinguished on the basis of their ε_Nd signatures. Two sides of what is classically considered one circulating Iapetus Ocean have different ε_Nd signatures from at least the Middle Cambrian until the Late Middle Ordovician. We infer two ocean basins between North America and Baltica separated by an island and/or shoal circulation barrier. Thus, it appears necessary to redefine the area of the Iapetus Ocean. The ε_Nd signature of the redefined smaller Iapetus Ocean ranges from −5 to −9 and the ε_Nd signature of the larger, coeval Panthalassa Ocean, including part of what was formerly called the Iapetus Ocean, ranges from −10 to −20. The first time that the ε_Nd values are identical in these two water masses is coincident with the onset of the Taconic Orogeny of North America. The paleogeographic geometry we infer from this work is consistent with paleogeographic reconstructions having the Baltica continent at very high latitudes in the Early/Middle Ordovician. The ε_Nd and faunal distribution support temperature-controlled conodont faunal provinciality. A rough mean age for exposed continental crust in the Early Paleozoic can be obtained from the average ε_Nd value of Early Paleozoic Oceans. The data suggest that the mean age of the crust as a function of time has remained essentially constant or even decreased during the past 500 Ma, and suggest substantial additions of new crust to the continents through the Phanerozoic.     

Conflicting Sm-Nd whole rock and U-Pb zircon ages for Archean lavas from Newton Township, Abitibi Belt, Ontario

Archean komatiitic and tholeiitic lavas from Newton Township, Ontario, have a sufficient range of Sm-Nd ratios to define a well-constrained line on the normal ¹⁴³Nd/¹⁴⁴Nd vs. ¹⁴⁷Sm/¹⁴⁴Nd isochron plot. The data give an isochron age of 2826 ± 64Ma, and an initial ε_Ndof+2.65 ± 0.26. However, U-Pb analysis of zircons from a dacitic volcaniclastic that underlies the komatiite-tholeiite suite give an age of 2697 ± 1.1Ma. There is strong evident that the zircon age is the eruption age, suggesting that the older Sm-Nd age is incorrect and probably results from mixing between isotopically distinct mantle sources. At the time of eruption, the sources had ε_Nd values from about +4.2 to +1.6, indicating that the Archean mantle in this area was markedly heterogeneous and not uniformly depleted.     

The Impact of the Herbicide Diuron on Photosynthesis in Three Species of Tropical Seagrass

The impact and recovery from exposure to the herbicide diuron [DCMU; 3-(3′,4′-dichlorophenyl)-1,1-dimethylurea] was assessed for three tropical seagrasses, maintained in outdoor aquaria over a 10-day period. Photosynthetic stress was detected using chlorophyll a fluorescence, measured with a Diving-PAM (pulse amplitude modulated fluorometer). Exposure to 10 and 100 μg l⁻¹ diuron resulted in a decline in effective quantum yield (ΔF/F_m^′) within 2 h of herbicide exposure in Cymodocea serrulata, Halophila ovalis and Zostera capricorni. Effective quantum yield also declined over the first 24 h of exposure in H. ovalis at even lower diuron concentrations (0.1 and 1.0 μg l⁻¹). Effective quantum yield in H. ovalis and Z. capricorni was significantly depressed at all diuron concentrations (0.1–100 μg l⁻¹) after 5 days exposure, whereas effective quantum yield in C. serrulata was only significantly lower in plants exposed to highest diuron concentrations (10 and 100 μg l⁻¹). Effective quantum yield depression was present 5 days after plants exposed to 10 and 100 μg l⁻¹ diuron were returned to fresh seawater. These results indicate that exposure to herbicide concentrations present in nearshore Queensland sediments present a potential risk to seagrass functioning.     

Neodymium isotopic study of Baffin Bay water: sources of REE from very old terranes

Water samples were collected from Baffin Bay and surrounding areas in order to evaluate this region as a potential source of Nd from old continental material to Atlantic water. The isotopic data ranged from ε_Nd(0) = −9.0 to −26 with most of the data around ε_Nd(0) = −20 compared with values of North Atlantic Deep Water (NADW) with ε_Nd(0) = −13.5. The concentration of Nd in Baffin Bay waters was as high as 6 × 10⁻¹² g/g compared with 2.5 × 10⁻¹² g/g for NADW. The combination of low ε_Nd and high Nd concentration indicates that Baffin Bay may be a significant source of Nd from very old crustal material. A simple box model was used to evaluate the contribution to the Nd budget of NADW and it was concluded that a substantial fraction of the Nd from ancient crustal sources that is required to maintain the isotopic composition of NADW could be supplied by Baffin Bay outflow.     

The early Paleozoic carbon cycle

A review of O, C, Sr and S isotope trends for the entire Phanerozoic shows that the present-day values of isotope signals are similar to those at the Proterozoic termination. The sharp rise in ⁸⁷Sr/⁸⁶Sr since 65 Ma has been attributed to an uplift and subsequent metamorphism and erosion associated with the Himalayas and Tibet. This orogenic evolution has been postulated to have influenced the global organic and inorganic carbon cycles and climate as well. A similar large-scale orogeny, the Pan-African event, also dominated the Neoproterozoic (Vendian) times, and the similarity of modern and Neoproterozoic isotope values for seawater may therefore have had a comparable tectonic cause. In this contribution, we present the results of a numerical model of the coupled C–alkalinity–S–Sr cycles suggesting that the early Paleozoic (from early Cambrian to late Devonian) evolution of Sr, O, C and S seawater isotope signals could have been the consequence of progressive oxidation of a large reduced carbon reservoir exhumed during the Pan-African orogeny. The δ¹⁸O measured in brachiopod shells is used as a forcing of the model, postulating that any change in the oxygen isotopic composition of seawater is the result of a disequilibrium in the organic carbon subcycle through the coupling of the oxygen isotopic and carbon cycles. The calculated δ¹³C, ⁸⁷Sr/⁸⁶Sr and δ³⁴S are in good agreement with the data, as is the reasonable calculated history for atmospheric pCO₂ and its relation to global climate.     

Evolution of glacial flow and drainage during the ablation season

Proglacial discharge is controlled by the geometry of the glacial drainage network and by meltwater processes. The glacial drainage systems of some alpine glaciers have been characterised using a model based on a proglacial discharge analysis. In this paper, we apply high frequency systemic analysis to data collected from the Baounet Glacier (French Alps) during two successive ablation seasons. Our approach is based on an analysis of the evolution of daily recession curves during the ablation period. The observed data are fitted by a single β-coefficient dependant recession law. Changes in β are compared to variations in the daily discharge amplitude and the time lag between air temperature and proglacial discharge. The changes in the β values do not appear to be related to changes in the time lag and the amplitude of the daily discharge. There were significant variations in the β-coefficient during the two ablation periods studied here even if there was no time lag or the daily discharge amplitude change. High values of β correspond to high drainage velocities; therefore increases in β values can be used as an indicator of the evolution of the glacier’s internal drainage network.     

Geochronology and Nd isotopic data of Grenville-age rocks in the Colombian Andes: new constraints for Late Proterozoic-Early Paleozoic paleocontinental reconstructions of the Americas

New UPb zircon crystallization ages and ⁴⁰Ar/³⁹Ar cooling ages from the Colombian Andes confirm the existence of rocks metamorphosed during the Orinoquian Orogenic Event (ca. 1.0 Ga) of northern South America. ε_Nd (t = 1.1 Ga) for these rocks range from −3.9 to +0.91, which is interpreted as a mixture of Late Archean-Early Proterozoic crust with juvenile material produced during the 1.1 Ga orogenic event. The Colombian Grenville age rocks are part of a much longer metamorphic pericratonal belt, sporadically exposed along the Andes, in western-central Peru, southern Bolivia and northern Argentina. In addition, Nd model (T_DM) ages for the Colombian rocks range from 1.9 to 1.45 Ga, similar to those obtained in the Grenville Province of the eastern U.S. and in the Mexican basement, placing constraints on Late Proterozoic-Early Paleozoic paleocontinental reconstructions.     

Recycling of the continental crust

In order to understand the evolution of the crust-mantle system, it is important to recognize the role played by the recycling of continental crust. Crustal recycling can be considered as two fundamentally distinct processes: 1) intracrustal recycling and 2) crust-mantle recycling. Intracrustal recycling is the turnover of crustal material by processes taking place wholly within the crust and includes most sedimentary recycling, isotopic resetting (metamorphism), intracrustal melting and assimilation. Crust-mantle recycling is the transfer of crustal material to the mantle with possible subsequent return to the crust. Intracrustal recycling is important in interpreting secular changes in sediment composition through time. It also explains differences found in crustal area-age patterns measured by different isotopic systems and may also play a role in modeling crustal growth curves based on Nd-model ages. Crustal-mantle recycling, for the most part, is a subduction process and may be considered on three levels. The first is recycling with only short periods of time in the mantle (<10 m.y.). This may be important in explaining the origin of island-arc and related igneous rocks; there is growing agreement that 1–3% recycled sediment is involved in their origin. Components of recycled crustal material, with long-term storage (up to 2.5 b.y.) in the mantle as distinct entities, has been suggested for the origin of ocean island and ultrapotassic volcanics but there is considerably less agreement on this interpretation. A third proposal calls for the return of crustal material to the mantle with efficient remixing in order to swamp the geochemical and isotopic signature of the recycled component by the mantle. This type of recycling is required for steady-state models of crustal evolution where the mass of the continents remains constant over geological time. It is unlikely if crust-mantle recycling has exceeded 0.75 km³/yr over the past 1–2 Ga.Good evidence exists that selective recycling is an important process. Sedimentary rocks preserved in different tectonic settings are apparently recycled at different rates, resulting in a bias in the sediment types preserved in the geologic record. Selective recycling has important implications for the interpretation of Nd model ages of old sedimentary rocks and in the analysis of accreted terranes. Although there is evidence that continental crust was formed prior to 3.8 Ga, the oldest preserved rocks do not exceed this age. It is likely that the intense meteorite bombardment, which affected the earth during the period 4.56–3.8 Ga, coupled with rapid mantle convection, which resulted from greater heat production, caused the destruction and probable recycling into the mantle of any early formed crust.Although crust-mantle recycling is seen as a viable process, it is concluded that crustal growth has exceeded crust-mantle recycling since at least 3.8 Ga. Intracrustal recycling has not been given adequate consideration in models of crustal growth based on isotopic data (particularly Nd model ages). It is concluded that crustal growth curves based on Nd model ages, while vastly superior to those based on K/Ar or Rb/Sr, tend to underestimate the volume of old crust, due to crust-mantle and/or intracrustal recycling.     

A high resolution palaeoclimatic record for the last 27,500 years in tropical West Africa from the carbon and nitrogen isotopic composition of lacustrine organic matter

Variations in the carbon and nitrogen isotopic composition of bulk organic matter in the sediments of Lake Bosumtwi, Ghana reflect climatically induced changes to the lake and the catchment flora. Cores spanning the last 27.5 kyr of sedimentation in the lake show large oscillations inδ¹³C_org PDB andδ¹⁵N_org Air. The late Pleistocene record is particularly detailed, showing changes of ca. 20‰ in carbon and ca. 10‰ in nitrogen isotopic compositions. These variations are of complex origin. Although different in magnitude, major isotopic excursions in the two records are generally in phase and reveal the occurrence of two major dry intervals at and immediately following the Last Glacial Maximum. The Allerød-Younger Dryas period also seems to have been marked by generally dry conditions in this part of tropical West Africa. Nitrogen isotopic evidence suggests that during the period 9.2–3.2 kyr the lake had an extremely stable water column, probably due to the absence of a windy or cool, dry season, or both. Regular circulation of the water column recommenced during the late Holocene and has persisted until the present day.     

A crystal-chemical basis for Pb retention and fission-track annealing systematics in U-bearing minerals, with implications for geochronology

This study develops an empirical crystal-chemical framework for systematizing the kinetics of Pb loss and fission-track annealing in U-bearing minerals. Ionic porosity, Z (the fraction of a mineral's unit-cell volume not occupied by ions) potentially accounts for kinetic behavior by monitoring mean metal-oxygen bond length/strength. Various tests of a general kinetics-porosity relationship are presented, based upon diverse mineral data including: (1) Pb diffusion parameters; (2) measured closure temperatures (T_C) for fission-track annealing and (3) retentivities of both Pb and fission tracks, from apparent-age data. Every kinetic parameter (including T_C and mineral age for both the U/Pb and fission-track systems) is inversely correlated with Z within the sub-assemblage: zircon (Z ≈ 29%), titanite ( 34%) and apatite ( 38%). Assuming a diffusional closure model, Pb isotopic transport phenomena are described by a T_C-Z scale “calibrated” with field-based T_C data for titanite (≥ 680 ± 20°C) and apatite ( 500°C). Extrapolation of this scale yields T_C estimates for the following minerals: staurolite (T_C ≥ 1060°C, Z ≈ 25%); garnet (≥ 1010°C, 26.5%); zircon (≥900°C); monazite, xenotime, and epidote (≥ 750°C, 32%); and Ca-clinopyroxene (≥ 670 ± 30°C, 34 ± 1%, depending on composition). These empirical results imply that a (U/)Pb/Pb date for staurolite or garnet records the time of mineral growth, not post-growth isotopic closure, as also concluded in recent field studies. Because Z systematizes fission-track annealing, this recrystallization process, like volume-diffusion, must also be rate-limited by the strength of chemical bonds. The extent to which other recrystallization processes are likewise rate-limited is important to U/Pb geochronology because they potentially compete with diffusion as mechanisms for Pb-isotopic resetting in nature.     

Enrichment of the continental lithosphere by OIB melts: Isotopic evidence from the volcanic province of northern Tanzania

Alkali basalts and nephelinites from the southern end of the East African Rift (EAR) in northern Tanzania have incompatible trace element compositions that are similar to those of ocean island basalts (OIB). They define a considerable range of Sr, Nd and Pb isotopic compositions (⁸⁷Sr/⁸⁶Sr= 0.7035−0.7058,ε_Nd = −5to+3, and²⁰⁶Pb/²⁰⁴Pb= 17.5−21.3), each of which partially overlaps the range found in OIB. However, they occupy a unique position in combined Nd, Sr and Pb isotopic compositional space. Nearly all of the lavas have radiogenic Pb, similar to HIMU with high time-integrated²³⁸U/²⁰⁴Pb coupled with unradiogenic Nd (+2 to −5) and radiogenic Sr (>0.704), similar to EMI. This combination has not been observed in OIB and provides evidence that these magmas predominantly acquired their Sr, Nd and Pb in the subcontinental lithospheric mantle rather than in the convecting asthenosphere. These data contrast with compositions for lavas from farther north in the EAR. The Pb isotopic compositions of basalts along the EAR are increasingly radiogenic from north to south, indicating a fundamental change to sources with higher time-integratedU/Pb, closer to the older cratons in the south. An ancient underplated OIB melt component, isolated for about 2 Ga as enriched lithospheric mantle and then remelted, could generate both the trace element and isotopic data measured in the Tanzanian samples. Whereas the radiogenic Pb in Tanzanian lavas requires a source with high time-integratedU/Pb, most continental basalts that are thought to have interacted with the continental lithospheric mantle have unradiogenic Pb, requiring a source with a history of lowU/Pb. Such lowU/Pb is readily accomplished with the addition of subduction-derived components, since the lower averageU/Pb of arc basalts (0.15) relative to OIB (0.36) probably reflects addition of Pb from subducted oceanic crust. If the subcontinental lithosphere is normally characterized by low time-integratedU/Pb it would appear that subduction magmatism is more important than OIB additions in supplying the Pb inventory of the lithospheric mantle. However,U/Pb ratios of xenoliths derived from the continental lithospheric mantle suggest that both processes may be important. This apparent discrepancy could be because xenoliths are not volumetrically representative of the subcontinental lithospheric mantle, or, more likely, that continental lithospheric mantle components in basalts are normally only identified as such when the isotopic ratios are dissimilar from MORB or OIB. Lithospheric enrichment from subaccreted OIB components appears to be more significant than generally recognized.     

Experimental determination of U and Th partitioning between clinopyroxene and natural and synthetic basaltic liquid

Clinopyroxene-silicate liquid partition coefficients for U and Th have been determined by particle track radiography from 1 atm crystallization experiments at controlledfO₂. Two natural basaltic and one synthetic composition were studied atfO₂ values from the NiNiO oxygen buffer to 1 log unit more oxidizing than FeFeO (IW+ 1). Over the range offO₂ values and compositions studied,D_U^cpx/liq = 0.0034–0.015,D_Th^cpx/liq = 0.008–0.036, andD_ThD_U= 3.4–1.1. With decreasingfO₂,D_ThD_U can decrease by up to a factor of 3 for a given composition, primarily from an increase inD_U^cpx/liq, which we interpret as resulting from an increase in the proportion of tetravalent U in the system with decreasingfO₂. This demonstrates that crystal-liquid UTh fractionation isfO₂ dependent and that U in terrestrial magmas is not entirely tetravalent.D_Th^cpx/liq appears to decrease in the two basalts at the lowestfO₂, possibly as a result of changes in composition withfO₂.

Our data show the sense of UTh fractionation by clinopyroxene-liquid partitioning is consistent with previous experimental determinations, in thatD_Th^cpxD_U^cpx> 1 in all cases. This indicates that, during partial melting, the liquid will have aTh/U ratio less than the clinopyroxene in the source. The observed²³⁸U²³⁰Th disequilibrium in MORB requires that the partial melt should have aTh/U ratio greater than the bulk source, and, therefore, cannot result from clinopyroxene-liquid partitioning. Further, the magnitudes of the measured partition coefficients are too small to generate significant UTh fractionation in either direction. Assuming that clinopyroxene contains the bulk of the U and Th in MORB source, our results indicate that²³⁸U²³⁰Th disequilibrium in MORB may not be caused by partial melting at all.     

The growth of the continent through geological time studied by Nd isotope analysis of shales

We determined the Nd isotopic composition and the Sm/Nd ratios in a series of Australian shales ranging from 0.2 Gy to 3.3 Gy. The first result of this study is the constancy of the Sm/Nd ratio in these shales, as in granitoids. Secondly, the initial (¹⁴³Nd/¹⁴⁴Nd) ratio gives a regular curve decreasing through geological time. Both results confirm that shales are representative samples of the continental crust, when insoluble elements, like REE, are studied.We calculated their Nd model ages of crustal differentiation. The model ages regularly decrease with the stratigraphic ages and after 2 Gy, the curve flattens and tends to an asymptotic value at around 1.8 Gy. The significance of the shales is that they represent a mixture of continental materials and we consider the model age of such a mixture directly linked with the mean age of the continental portion feeding the sedimentary basin.From these results, we deduce a quantitative model of the growth curve of the continental source of the shales taking into account the effects of erosion which selectively sample recent mountains relative to shield areas. We propose that the results obtained here are representative of the whole Gondwana continent.Having studied the case of the Australian shales, we try to extend our study. First we applied our quantitative approach to the recent results obtained by O'Nions et al. on North Atlantic provinces. The continental growth curves obtained by our inversion procedure are quite distinct from the Australian shales showing the regional character of shales.With these two cases studied we try to compare our results with the already developed model for continental growth. The consideration of the surface conservative versus surface non-conservative models clearly show the non-uniqueness of the geological interpretation of the growth curve. On the other hand, we have calculated for each case the recycling rate versus geological time by comparing the growth curve with the Hurley-Rand province age curve. Such recycling increases with time in agreement with the data obtained on Nd and Sr initial ratios on granitoids.     

The Vendian record of Sr and C isotopic variations in seawater: Implications for tectonics and paleoclimate

New Sr and C isotopic data, both obtained on the same samples of marine carbonates, provide a relatively detailed record of isotopic variation in seawater through the latest Proterozoic and allow, for the first time, direct correlation of these isotopic changes in the Vendian ( 540–610 Ma). The strong isotope variations determined in this study record significant environmental and tectonic changes. Together with a fairly poorly constrained Nd isotopic record, the Sr and C isotopic records can be used to constrain rates of erosion, hydrothermal alteration and organic C burial. Further, comparison of these records with those of the Cenozoic permit investigation of the general relationship between global tectonics and continental glaciation. In particular, results of this study show a very large change in the ⁸⁷Sr/⁸⁶Sr of marine carbonates from low pre-Vendian ( > 610 Ma) values ( 0.7066) to high Middle Cambrian values ( 0.7090). This change is greater in magnitude than the significant increase in seawater ⁸⁷Sr/⁸⁶Sr through the Cenozoic. Both changes are attributed to high erosion rates associated with continent-continent collisions (Pan-African and Himalayan-Tibetan). In the latest Proterozoic these high erosion rates, probably coupled with high organic productivity and anoxic bottom-water conditions, contributed to a significant increase in the burial rate of organic C. Ice ages mark both the Neoproterozoic and Cenozoic, but different stratigraphic relationships between the Sr isotopic increase and continental glaciation indicate that uplift-driven models proposed to explain Cenozoic climatic change cannot account for the latest Proterozoic ice ages.     

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.