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1.
Hafnium isotopes in Arctic Ocean water   总被引：1，自引：0，他引：1  
The first isotopic compositions of dissolved hafnium in seawater from across the Arctic Ocean are reported. Most samples from the four sub-basins of the Arctic Ocean have values within error of an average of εHf = +0.8. Combined Hf-Nd isotope compositions do not fall on the well-established positive correlation for mantle and crustal rocks. Instead, Arctic waters have Hf that is more radiogenic than that typically found in rocks with similar Nd isotope compositions, a feature previously found in ferromanganese crusts and waters from the Pacific Ocean. Arctic seawater samples generally fall on the lower part of the ferromanganese crust array, reflecting influences of inputs from Arctic rivers and interactions of shelf waters with underlying sediments. Arctic rivers have much higher Hf concentrations (7-30 pM) than Arctic seawater (0.36-4.2 pM). Water from the Mackenzie River has the least radiogenic Hf, with εHf = −7.1 ± 1.7, and plots furthest away from the ferromanganese crust array, while waters from the Ob, Yenisey, and Lena Rivers have values that are indistinguishable from most Arctic waters. In the Amundsen, Makarov, and Canada basins, Hf concentrations are highest at the surface and lowest in the deeper waters, reflecting the influences of riverine inputs and of waters that have flowed over the extensive Siberian continental shelves and have Nd and Hf characteristics that reflect water-sediment interactions. This is in contrast to the relatively low near surface Hf concentrations reported for locations elsewhere. The Pacific water layer in the Canada Basin exhibits the highest value of εHf = +6.8 ± 1.8, reflecting the Hf isotopic composition of waters entering the Arctic from the Pacific Ocean. Mixing relationships indicate that a substantial fraction of the Hf in the Mackenzie River is lost during estuarine mixing; the behaviour of Hf from other rivers is less constrained.  相似文献   

2.
The neodymium concentration, CNd, and isotopic composition, εNd, in seawater have been determined in the water column at five sites in the Barents Sea-Fram Strait area where most of the water exchange between the Arctic Ocean and the North Atlantic takes place. In the main Arctic Ocean inflow branch across the Barents Sea the concentration and isotopic composition (CNd = 15.5 pmol/kg and εNd = −10.8) are similar to those reported for the northeastern Nordic Seas, which is consistent with this region being a source area for the Arctic inflow. Due to the addition of Nd from Svalbard shelf sediments, the CNd in the surface waters above 150 m, in the Fram Strait inflow branch is higher by a factor of 2 and the εNd is shifted to lower values (−11.8).In the stratified Nansen Basin, where cold low salinity water overlies warmer Atlantic water the CNd and εNd do not vary with the vertical temperature-salinity structure but are essentially constant and similar to those of the Atlantic inflow throughout the entire water column, down to 3700 m depth, which indicates that the Nd is to a large extent of Atlantic origin.Compared to the Atlantic inflow water, the Nd in the major Arctic Ocean outflow, the Fram Strait, show higher CNd in the surface waters above 150 m, and a higher εNd (−9.8) throughout the entire water column down to 1300 m depth. Sources for the more radiogenic Nd isotopic composition in deep water of the Fram Strait outflow most likely involve boundary exchange with sediments on the shelf and slope as the water passes along the Canadian archipelago. River water is a possible source in the surface water but it also seems likely that Pacific water Nd, modified by interactions on the shelf, is an important component in the Fram Strait surface outflow. Changes in the relative proportions of inflow of river water and flow of Pacific water through the Arctic Ocean could thus influence the isotopic composition of Nd in the North Atlantic.  相似文献   

3.
Three vertical profiles of seawater concentration and isotopic composition of Nd were determined for the western to central North Pacific Ocean.In the subarctic oceanic region, at depths greater than 500 m, one vertical profile of Nd isotopic composition was indistinguishable from most previously reported profiles from here. The data indicate a rather homogeneous Nd isotopic composition in the subarctic oceanic region at middle to deep depths (>500 m). Two stations in the subtropical oceanic region exhibited similar Nd isotopic composition profiles to those previously reported. The maxima εNd values at depths of 800-1000 m (εNd = −3.4 to −2.7), which correspond to the North Pacific Intermediate Water (NPIW), are found at both subtropical stations. This implies a ubiquitous distribution of NPIW showing a radiogenic εNd value in the North Pacific. The subsurface minimum at a depth of ∼200 m, which indicates the penetration of the North Pacific Tropical Water (NPTW) with an unradiogenic Nd isotopic signal, was observed at one station in the western Pacific. This station had much lower εNd than the central station at depths around 5000 m, suggesting the greater prominence of Antarctic Bottom Water (AABW) in the western subtropical Pacific than in the central to eastern subtropical Pacific.Results of a model calculation assuming boundary exchange indicate that the Hawaiian Islands play an important role in supplying radiogenic Nd to the central Pacific, similar to some continental margins.We show that Nd isotopic composition is a versatile tracer for ocean circulation and the geochemical cycle of Nd in the North Pacific. Further studies on the distribution of Nd isotopic composition in the Pacific Ocean, including the Southern Pacific, will better elucidate the circulation and geochemical cycle of Nd in the Pacific.  相似文献   

4.
Four vertical profiles of the concentration and isotopic composition of Nd in seawater were obtained in the western North Pacific. Two profiles from the Kuroshio Current regime showed congruently that although the Nd concentration increases gradually with depth, its isotopic composition varies significantly with depth depending upon the water mass occupying the water column. The high-salinity Kuroshio waters originating from the North Pacific Tropical Water (NPTW) carry the least radiogenic Nd (?Nd = −7.4 to −8.7) to this region at ∼250 m from the western margin continental shelves, most likely from the East China Sea. The Nd isotopic compositions in the North Pacific Intermediate Water (NPIW) that occurs at 600 to 1000 m in the subtropical region are fairly uniform at ?Nd = −3.7. The profile data from the ∼38° to 40°N Kuroshio/Oyashio mixed water region off Sanriku of Honshu, Japan, also suggest that the newest NPIW with ?Nd = −3.2 is formed there by the mixing of various source waters, and the radiogenic component of Nd is derived mainly from the Oyashio waters.In the Pacific Deep Water (PDW) below ∼1000 m, the Nd isotopic composition is neither vertically nor horizontally homogeneous, suggesting that it serves as a useful tracer for sluggish deep water circulation as well. Two profiles from the Izu-Ogasawara Trench showed a minimum ?Nd value at ∼2000 m, suggesting that there exists a horizontal advective flow in the vicinity of Honshu, Japan. There is some evidence from other chemical properties to support this observation. The waters below 4000 m including those within the trench in the subtropical region have ?Nd values of around −5, suggesting that the deep waters are fed from the south along the western boundary, ultimately from the Antarctic Bottom Water (AABW) in the South Pacific. This extends up to ∼40°N along the Japanese Islands. In the subarctic region (>∼42°N), the waters have more radiogenic Nd with ?Nd > −4.0 throughout the water column, presumably due to the supply of Nd by weathering in such igneous provinces as the Kuril-Kamchatska-Aleutian Island chain. The lateral inhomogeneity of the Nd isotopic composition in PDW suggests that there may be different circulation and mixing regimes in the North Pacific Basin.  相似文献   

5.
We present the first comprehensive set of dissolved 10Be and 9Be concentrations in surface waters and vertical profiles of all major sub-basins of the Arctic Ocean, which are complemented by data from the major Arctic rivers Mackenzie, Lena, Yenisey and Ob. The results show that 10Be and 9Be concentrations in waters below 150 m depth are low and only vary within a factor of 2 throughout the Arctic Basin (350-750 atoms/g and 9-15 pmol/kg, respectively). In marked contrast, Be isotope compositions in the upper 150 m are highly variable and show systematic variations. Cosmogenic 10Be concentrations range from 150 to 1000 atoms/g and concentrations of terrigenous 9Be range from 7 to 65 pmol/kg, resulting in 10Be/9Be ratios (atom/atom) between 0.5 and 14 × 10−8. Inflowing Atlantic water masses in the Eurasian Basin are characterized by a 10Be/9Be signature of 7 × 10−8. The inflow of Pacific water masses across the Bering Strait is characterized by lower ratios of 2-3 × 10−8, which can be traced into the central Arctic Ocean, possibly as far as the Fram Strait. A comparison of the high dissolved surface 10Be and 9Be concentrations (corresponding to low 10Be/9Be signatures of ∼2 × 10−8) in the Eurasian Basin with hydrographic parameters and river data documents efficient and rapid transport of Be with Siberian river waters across the Siberian Arctic shelves into the central Arctic Basin, although significant loss and exchange of Be on the shelves occurs. In contrast, fresh surface waters from the Canada Basin also show high cosmogenic 10Be contents, but are not enriched in terrigenous 9Be (resulting in high 10Be/9Be signatures of up to 14 × 10−8). This is explained by a combination of efficient scavenging of Be in the Mackenzie River estuary and the shelves and additional supply of cosmogenic 10Be via atmospheric fallout and melting of old sea ice. The residence time of Be in the deep Arctic Ocean estimated from our data is 800 years and thus similar to the average Be residence time in the global ocean.  相似文献   

6.
The hafnium isotope composition of Pacific Ocean water   总被引：1，自引：0，他引：1  
The first Hf isotope data for seawater are reported for a series of stations in the Northwestern Pacific and define a range from εHf = 3.5 ± 1.4 to 8.6 ± 1.6. Most samples have values within error of the average of εHf = 5.9, but significant variations are found in intermediate waters at a depth of 600 m, as well as in deep waters. The Nd and Hf isotope compositions of the deep waters fall within the range of values found for surfaces of hydrogenetic ferromanganese crusts in the region, confirming that Hf in the Fe-Mn crusts has been derived from the overlying water column, which thus provide an archive of past seawater compositions. Although the seawater samples are generally close to the global εNd-εHf correlation obtained from ferromanganese crusts, there are significant deviations from this correlation indicating that there is some additional decoupling between Nd and Hf isotope signals, most likely caused by local water mass mixing and differences in residence times. This is not resolved in the crust samples, which integrate seawater signals over 104 years. The combined use of these two isotope systems in seawater therefore provides an additional dimension for tracing water masses in the oceans. Studies of the distribution of oceanic Hf isotope compositions that have been confined to deep water and boundary waters, as recorded in seafloor ferromanganese crusts, can now be extended and aimed at characterising the entire present-day water column. Average Hf concentrations measured in this study are somewhat lower than previously reported, suggesting a shorter residence time for Hf in the global oceans, although the uncertainty in the extent of Hf removal from the water column during estuarine mixing as well as a lack of data on hydrothermal and dust inputs remains a limit on how well the residence time can be defined.  相似文献   

7.
We have carried out a comparative Rb-Sr, Sm-Nd and Lu-Hf isotopic study of a progressively deformed hercynian leucogranite from the French Massif Central, belonging to the La Marche ductile shear zone, in order to investigate the respective perturbation of these geochronometers with fluid induced deformation. The one-meter wide outcrop presents a strongly deformed and mylonitized zone at the center, and an asymmetric deformation pattern with a higher deformation gradient on the northern side of the zone. Ten samples have been carefully collected every 10 cm North and South away from the strongest deformed mylonitic zone. They have been analyzed for a complete major, trace element data set, oxygen isotopes, Rb-Sr, Sm-Nd and Lu-Hf isotopic systematics.We show that most of major and trace elements except SiO2, alkaline elements (K2O, Rb), and some metal transition elements (Cu), are progressively depleted with increasing deformation. This depletion includes REE + Y, but also HFS elements (Ti, Hf, Zr, Nb) which are commonly considered as immobile elements during upper level processes. Variations in elemental ratios with deformation, e.g. decrease in LREE/MREE- HREE, Nd/Hf, Th/Sr, increase in Rb/Sr, U/Th and constant Sr/Nd, lead to propose the following order of element mobility: U ? Th > Sr = Nd ? Hf + HREE. We conclude in agreement with previous tectonic and metallogenic studies that trace element patterns across the shear zone result from circulation of oxidizing F-rich hydrothermal fluids associated with deformation. A temperature of the fluid of 470-480 °C can be deduced from the δ18O equilibrium between quartz-muscovite pairs.Elemental fractionation induces perturbation of the Rb-Sr geochronometer. The well-defined 87Rb/86Sr-87Sr/86Sr correlation gives an apparent age of 294 ± 19 Ma, slightly younger than the 323 ± 4 Ma age of leucogranites in this area. This apparent age is interpreted as dating event of intense deformation and fluid circulation associated with mass transfer, and exhumation of the ductile crust shortly after the leucogranite emplacement. Sm-Nd and Lu-Hf isochron-type diagrams do not define any correlation, because of the low fractionated Sm/Nd and Lu/Hf ratios. Isotopic data demonstrate that only the Lu-Hf geochronometer system is not affected by fluid circulation and gives reliable TDM age (1.29 ± 0.03 Ga) and εHf signatures. By contrast, the Sm-Nd geochronometer system gives erroneous old TDM ages of 2.84-4 Ga. There is no positive εNd-εHf correlation, because of decreasing εNd values with deformation at constant εHf values. However, εNd-εHf values remain in the broad εNd-εHf terrestrial array, which strongly indicates that fluid-induced fractionation can contribute to the width of the terrestrial array. The strong εHf negative values of the leucogranite are similar to metasedimentary granulitic xenoliths from the French Massif Central and confirm the generation of the leucogranite by several episodes of reworking of the lower crust.  相似文献   

8.
Neodymium (Nd) isotope profiles were analyzed on two Baltic Mn/Fe precipitates (99/2 and TL1) from shallow water (20 m) of the Mecklenburg Bay. The age range of these Mn/Fe precipitates determined by 226Raex/Ba dating reaches from recent growth back to ∼4300 and 1000 yr BP, respectively. Over this time range, the Nd isotope composition varies from εNd (0) = −13.1 to −17.5 in the selected Baltic precipitates indicating substantial changes in the Nd isotope composition of the Baltic Sea. The lowest εNd values were recorded during the time interval of the Little Ice Age (LIA, AD ∼1350 to 1850). These minimum values indicate either an increase of the input of less radiogenic Nd from Scandinavian Archean-Proterozoic sources (εNd about −22) to the Baltic Sea or a decrease of the input of more radiogenic Nd from continental European sources (εNd about −12) and/or North Sea water (εNd about −10). Variations of both, erosive continental input and North Sea inflow may indicate a direct response of the Nd isotope signal in the Baltic Sea to climate changes during the LIA and be related to cyclic shifts in the atmospheric circulation triggered by the North Atlantic Oscillation (NAO). Another aspect that possibly influenced the input of trace elements and Nd isotopes into the Baltic Sea is the population development in the circum Baltic area during the LIA. The lowest εNd values also correspond to the medieval demographic crises that led to a significant decrease of agricultural activity and farmland. The reduction of soil erosion and enhanced regrowth of natural vegetation may have changed the amount and proportions of dissolved and suspended particulate matter transported into the Baltic Sea by rivers which in turn may have resulted in a change of the Nd isotope composition of Baltic Sea water.  相似文献   

9.
The chemical composition of surface water in the photic zone of the Precambrian ocean is almost exclusively known from studies of stromatolitic carbonates, while banded iron formations (IFs) have provided information on the composition of deeper waters. Here we discuss the trace element and Nd isotope geochemistry of very shallow-water IF from the Pongola Supergroup, South Africa, to gain a better understanding of solute sources to Mesoarchean shallow coastal seawater. The Pongola Supergroup formed on the stable margin of the Kaapvaal craton ∼2.9 Ga ago and contains banded iron formations (IFs) that represent the oldest documented Superior-type iron formations. The IFs are near-shore, pure chemical sediments, and shale-normalized rare earth and yttrium distributions (REYSN) exhibit positive LaSN, GdSN, and YSN anomalies, which are typical features of marine waters throughout the Archean and Proterozoic. The marine origin of these samples is further supported by super-chondritic Y/Ho ratios (average Y/Ho = 42). Relative to older Isua IFs (3.7 Ga) from Greenland, and younger Kuruman IFs (2.5 Ga) also from South Africa, the Pongola IFs are depleted in heavy rare earth elements (HREE), and appear to record variations in solute fluxes related to sea level rise and fall. Sm-Nd isotopes were used to identify potential sediment and solute sources within pongola shales and IFs. The ?Nd(t) for Pongola shales ranges from −2.7 to −4.2, and ?Nd(t) values for the coeval iron-formation samples (range −1.9 to −4.3) are generally indistinguishable from those of the shales, although two IF samples display ?Nd(t) as low as −8.1 and −10.9. The similarity in Nd isotope signatures between the shale and iron-formation suggests that mantle-derived REY were not a significant Nd source within the Pongola depositional environment, though the presence of positive Eu anomalies in the IF samples indicates that high-T hydrothermal input did contribute to their REY signature. Isotopic mass balance calculations indicate that most (?72%) of the Nd in these seawater precipitates was derived from continental sources. If previous models of Fe-Nd distributions in Archean IFs are applied, then the Pongola IFs suggest that continental fluxes of Fe to Archean seawater were significantly greater than are generally considered.  相似文献   

10.
We present hafnium (Hf) and neodymium (Nd) isotopic compositions and concentrations in surface waters of the eastern Atlantic Ocean between the coast of Spain and South-Africa. These data are complemented by Hf and Nd isotopic and concentration data, as well as rare earth element (REE) concentrations, in Saharan dust.Hafnium concentrations range between a maximum of 0.52 pmol/kg in the area of the Canary Islands and a minimum value of 0.08 pmol/kg in the southern Angola Basin. Neodymium concentrations also show a local maximum in the area of the Canary Islands (26 pmol/kg) but are even higher between ∼20°N and ∼4°N reaching maximum concentrations of 35 pmol/kg. These elevated concentrations provide evidence of inputs from weathering of the Canary Islands and from the partial dissolution of dust from the Sahara/Sahel region. The inputs from ocean island weathering are also reflected in radiogenic Hf and Nd isotopes.The Hf isotopic compositions of dust samples themselves are highly variable, ranging between εHf = −20 and −0.6. The combined Hf and Nd isotopic compositions of dust plot close to the “terrestrial array” during periods of appreciable dust load in the atmosphere. During low atmospheric dust loading combined Hf and Nd isotopic compositions similar to seawater are observed. Most of the variability can be explained in terms of variable degrees of zircon loss from the dust samples, which in turn is linked to sorting during atmospheric transport to the eastern Atlantic Ocean and possibly presorting by sedimentary redistribution on the continent. In addition, increasing relative proportions of radiogenic clay minerals with decreasing grain size may contribute to the radiogenic Hf isotopic compositions observed.While the Nd isotopic composition in the surface ocean reflects the Nd isotopic composition of the Saharan dust adjacent to the Sahara/Sahel region, the release of Hf from that dust appears to be incongruent and results in surface ocean Hf isotopic compositions which are ∼10 εHf more radiogenic than the bulk dust. Radiogenic Hf appears to be released from clays and possibly from trace apatite. Rare earth element patterns of dust samples indicate the presence of apatite but provide no evidence for ferromanganese grain coatings, suggesting that such coatings are insignificant in the release of Hf and Nd from Saharan dust to the surface ocean.The Nd isotopic composition of the surface waters becomes less radiogenic south of the equator, most likely reflecting the release of Nd from Congo river sediments. The release of Hf from Saharan dust and the Congo river sediments, however, does not produce distinct Hf isotopic signatures in the surface ocean, implying that the mobile fraction of Hf integrated over large continental areas is isotopically uniform. The Hf isotopic uniformity in the surface ocean means that the limited variability in deep water isotopic compositions is consistent with a short deep water residence time and reflects homogenous continental inputs rather than efficient deep water homogenization.  相似文献   

11.
Silicate Nd-Sr isotopes of the fine-grained fractions of the 10 major deserts and sandy lands in North China and the loess in Chinese Loess Plateau were systematically investigated. Wide ranges in Nd-Sr isotopic compositions have been observed. The results of the <75 μm silicate fractions show that the Nd-Sr isotopic compositions of each desert are quite homogeneous and unique. According to the geographic distribution of the deserts and their Nd-Sr isotopes of both the <75 and <5 μm silicate fractions, three isotopic regions of Chinese deserts can be identified: (A) the deserts on the northern boundary of China, with the highest εNd(0) > −7.0; (B) the deserts on the northern margin of Tibetan Plateau, with εNd(0) ranging from −11.9 to −7.4; and (C) the deserts on the Ordos Plateau, with the lowest εNd(0) < −11.5. The distribution of the threes isotopic regions is controlled by the tectonic setting in North China, which implies that the materials of the deserts are derived from the locally eroded rocks from the surrounding mountains and the Nd-Sr isotopic signatures of these deserts could be quit stable over the past million years on the sub-tectonic time scales if there is any desert at those times. The Nd-Sr isotopic compositions of the loess are mostly close to those of the deserts in isotopic region B, suggesting that the main source regions of the last glacial loess in the Chinese Loess Plateau are Badain Jaran Desert, Tengger Desert, and Qaidam Desert. Also, the comparison between the Nd-Sr isotopes of the <5 μm silicate fractions of the deserts and the ancient dust falls in the North Pacific and Greenland show that the Asian end members of these dust falls are derived most from the deserts in the isotopic region B and less from those in the isotopic region C.  相似文献   

12.
Nine depth-profiles of dissolved Nd concentrations and isotopic ratios (εNd) were obtained in the Levantine Basin, the Ionian, the Aegean, the Alboran Seas and the Strait of Gibraltar. Thirteen core-top sediments and Nile River particle samples were also analyzed (leached with 1 N HCl, acetic acid or hydroxylamine hydrochloride). The seawater εNd values become more radiogenic during the eastward circulation in the Mediterranean Sea. The relationship between salinity and the seawater εNd shows that the Nd isotopic signature is more conservative than salinity in the Mediterranean Sea. The water mass with the highest εNd (−4.8) is found at about 200 m in the easternmost Levantine basin. The average εNd value for deep waters is −7.0 in the eastern basin, 2.5 ε-units higher than in the western basin. By examining the sensitivity of seawater εNd to Nd inputs from the Nile, we conclude that the most significant radiogenic Nd source is partially dissolved Nile River particles. The Nd flux from the Nile River water has a minor influence on the Mediterranean seawater εNd. Except for the easternmost Levantine Basin, the leachate εNd values are consistent with the seawater values. In the easternmost Levantine Basin, the leachate εNd values obtained with HCl leaching are systematically higher than the seawater values. The relationship between leachate and residual εNd values indicates that the HCl leaching partially dissolves lithogenic Nd, so the dissolution of Nile River particles is the cause of the observed shift. Some εNd values obtained with hydroxylamine hydrochloride leaching are higher than those obtained with HCl leaching. Although the reason for this shift is not clear, 87Sr/86Sr successfully detects the presence of a nonmarine component in the leachate. Our results suggest that leaching performance may vary with the mineralogy of marine sediments, at least in the case of the Mediterranean Sea.  相似文献   

13.
A combined study including apatite geochemistry, zircon U-Pb, Lu-Hf isotopes and whole-rock geochemistry including Nd isotopes was carried out for the late Mesozoic volcanic rocks from the Luzong Basin, in the lower Yangtze River region, South China. Whole-rock geochemistry indicates the enrichments of large ion lithophile elements (LILE) and light rare earth elements (LREE) as well as depletions of Nb, Ta and Ti. The extremely low Cl contents in apatites strongly contrast with the rather high-K contents in whole rocks. Potential loss of Cl during syn- and post-magmatic processes having been ruled out, Cl-K decoupling is attributed to be a feature inherited from the primary magma, which indicates the involvement of highly dehydrated sediments and altered oceanic crust in the mantle source. A calculation based on apatite and whole-rock geochemistry further illustrates that the source was composed of four end-members in the perspective of Cl/K, Cl/Nb and F/K ratios. The Hf-Nd isotopes are decoupled for the basaltic trachytes from the lower volcanic sequences in the Luzong Basin, with rather low εHf(t) values (mean = − 10.3) and inconsistent Hf-Nd model ages (Hf ~ 1.8 Ga, Nd ~ 1.3 Ga), which indicate the “zircon effect” that in turn requires the incorporation of continental detritus in the source via subduction. However, Hf and Nd isotopes are nearly coupled for the rocks from the upper volcanic sequences in the Luzong Basin. Late-Mesoproterozoic two-stage Hf and Nd model ages (ca. 1.2 Ga) of rocks from the upper volcanic sequences in the Luzong Basin are similar to those of the Neoproterozoic igneous rocks from the Jiangnan orogen, suggesting their relationship with the same subduction event. Based on the combined apatite geochemistry and Hf-Nd isotopes, this work suggests that the source of Luzong volcanic rocks might incorporate Neoproterozoic subducted slab fragments and detrital sediments that had been blocked in the deep lithospheric mantle below the Luzong area since the Neoproterozoic assembly between the Yangtze and Cathaysia blocks. The partial melting may be triggered by the back-arc lithospheric extension related to the subduction of Paleo-Pacific plate in the late Mesozoic.  相似文献   

14.
Neodymium isotopic compositions (εNd) have been largely used for the last fifty years as a tracer of past ocean circulation, and more intensively during the last decade to investigate ocean circulation during the Cretaceous period. Despite a growing set of data, circulation patterns still remain unclear during this period. In particular, the identification of the deep-water masses and their spatial extension within the different oceanic basins are poorly constrained. In this study we present new deep-water εNd data inferred from the Nd isotope composition of fish remains and Fe–Mn oxyhydroxide coatings on foraminifera tests, along with new εNd data of residual (partly detrital) fraction recovered from DSDP Sites 152 (Nicaraguan Rise), 258 (Naturaliste Plateau), 323 (Bellinghausen Abyssal Plain), and ODP Sites 690 (Maud Rise) and 700 (East Georgia Basin, South Atlantic). The presence of abundant authigenic minerals in the sediments at Sites 152 and 690 detected by XRD analyses may explain both middle rare earth element enrichments in the spectra of the residual fraction and the evolution of residual fraction εNd that mirror that of the bottom waters at the two sites. The results point towards a close correspondence between the bottom water εNd values of Sites 258 and 700 from the late Turonian to the Santonian. Since the deep-water Nd isotope values at these two sites are also similar to those at other proto-Indian sites, we propose the existence of a common intermediate to deep-water mass as early as the mid-Cretaceous. The water mass would have extended from the central part of the South Atlantic to the eastern part of proto-Indian ocean sites, beyond the Kerguelen Plateau. Furthermore, data from south and north of the Rio Grande Rise–Walvis Ridge complex (Sites 700 and 530) are indistinguishable from the Turonian to Campanian, suggesting a common water mass since the Turonian at least. This view is supported by a reconstruction of the Rio Grande Rise–Walvis Ridge complex during the Turonian, highlighting the likely existence of a deep breach between the Rio Grande Rise and the proto-Walvis Ridge at that time. Thus deep-water circulation may have been possible between the different austral basins as early as the Turonian, despite the presence of potential oceanic barriers. Comparison of new seawater and residue εNd data on Nicaraguan Rise suggests a westward circulation of intermediate waters through the Caribbean Seaway during the Maastrichtian and Palaeocene from the North Atlantic to the Pacific. This westward circulation reduced the Pacific water influence in the Atlantic, and was likely responsible for more uniform, less radiogenic εNd values in the North Atlantic after 80 Ma. Additionally, our data document an increasing trend observed in several oceanic basins during the Maastrichtian and the Palaeocene, which is more pronounced in the North Pacific. Although the origin of this increase still remains unclear, it might be explained by an increase in the contribution of radiogenic material to upper ocean waters in the northern Pacific. By sinking to depth, these waters may have redistributed to some extent more radiogenic signatures to other ocean basins through deep-water exchanges.  相似文献   

15.
Stratigraphic changes in the εNd of epeiric sea carbonates from central North America track the submergence history of the interior craton during the Late Ordovician. Fluctuations in sea level changed the Nd isotope balance of the epeiric sea by modifying the flux of Nd weathered from the highlands of the Taconic Orogen (εNd = −6 to −9) and from the low relief Precambrian basement (εNd = −22 to −15) of the Transcontinental Arch and Canadian Shield. Transgressions over the Arch and Shield, which diminished the weathering flux of Nd from the Precambrian basement, are recorded as positive shifts in the εNd profiles of carbonates. Negative εNd shifts reflect regression and reexposure of the Precambrian basement to erosion. Correlation of Upper Ordovician carbonates by use of the εNd profiles demonstrates the potential for Nd isotope stratigraphy. Comparison of stratigraphic variations in carbonate Sm/Nd ratios with sea level curves, conodont paleoecology, and the εNd profiles suggest that our observed variations in Sm/Nd ratios are related to changes in depth. Increasing Sm/Nd ratios correlate with increasing depth, whereas decreasing Sm/Nd ratios correlate with decreasing depth. This relationship between Sm/Nd ratios and depth suggests Sm/Nd profiles have potentially wide applications in understanding the paleoceanography of ancient epeiric seas.  相似文献   

16.
Silicon isotopes in dissolved silicic acid were measured in the upper four kilometers between 4°N and 3°S latitude at 110°W longitude in the eastern Equatorial Pacific. Silicon isotopes became progressively heavier with silicic acid depletion of surface water as expected from biological fractionation. The value of ε estimated by applying a steady-state isotope fractionation model to data from all stations between 4°N and 3°S was −0.77 ± 0.12‰ (std. err.). When the analysis was restricted to those stations whose temperature and salinity profiles indicated that they were directly influenced by upwelling of the Equatorial Undercurrent (EUC), the resulting value of ε was −1.08 ± 0.27‰ (std. err.) similar to the value established in culture studies (−1.1‰). When the non steady state Rayleigh model was applied to the same restricted data set the resulting value of ε was significantly more positive, −0.61 ± 0.16‰ (std. err.). To the extent that the equatorial system approximates a steady state these results support a value of −1.1‰ for the fractionation factor for isotopes of Si in the sea. Without the assumption of steady state the value of ε can only be constrained to be between −0.6 and −1.1‰. Silicic acid in Equatorial Pacific Deep Water below 2000 m had a near constant δ30Si of +1.32 ± 0.05‰. That value is significantly more positive than obtained for North Pacific Deep Water at similar depths at stations to the northwest of our study area (0.9-1.0‰) and it is slightly less positive than new measures of the δ30Si of silicic acid from the silicic acid plume centered over the Cascadia basin in the Northeast Pacific (Si(OH)4 > 180  μM, δ30Si = +1.46 ± 0.12‰ (SD, n = 4). We show that the data from the equator and Cascadia basin fit a general trend of increasing δ30Si(OH)4 with increasing silicic acid concentration in the deep sea, but that the isotope values from the Northeast Pacific are anomalously light. The observed level of variation in the silicon isotope composition of deep waters from this single ocean basin is considerably larger than that predicted by current models based on fractionation during opal formation with no isotope effect during dissolution. Confirmation of such high variability in deep water δ30Si(OH)4 within individual ocean basins will require reassessment of the mechanisms controlling the distribution of isotopes of silicon in the sea.  相似文献   

17.
An Early Permian volcanic assemblage is well exposed in the central-western part of the Apuseni Mountains (Romania). The rocks are represented by rhyolites, basalts and subordinate andesites suggesting a bimodal volcanic activity that is intimately associated with a post-orogenic (Variscan) syn-sedimentary intra-basinal continental molasse sequences. The mafic and mafic-intermediate rocks belong to sub-alkaline tholeiitic series were separated in three groups (I–III) showing a high Th and Pb abundances, depletion in Nb, Ta and Sr, and slightly enriched in LREE patterns (LaN/YbN = 1.4–4.4). Isotopically, the rocks of Group I have the initial ratios 87Sr/86Sr(i) = 0.709351–0.707112, 143Nd/144Nd(i) = 0.512490–0.512588 and high positive ?Nd270 values from 3.9 to 5.80; the rocks of Group II present for the initial ratios values 87Sr/86Sr(i) = 0.709434–0.710092, 143Nd/144Nd(i) = 0.512231–0.512210 and for ?Nd270 the negative values from −1.17 to −1.56; the rocks of Group III display for the initial ratios the values 87Sr/86Sr(i) = 0.710751–0.709448, 143Nd/144Nd(i) = 0.512347–0.512411 and for ?Nd270 the positive values from 1.64 to 2.35. The rocks resembling continental tholeiites, suggest a mantle origin and were further affected by fractionation and crustal contamination. In addition, the REE geochemistry (1 > SmN/YbN < 2.5; 0.9 > LaN/SmN < 2.5) suggests that these rocks were generated by high percentage partial melting of a metasomatized mantle in the garnet peridotite facies. The felsic rocks are enriched in Cs, Rb Th and U and depleted in Nb, Ta, Sr, Eu, and Ti. The REE fractionation patterns show a strong negative Eu anomaly (Eu/Eu* = 0.23–0.40). The felsic rocks show the initial ratios the values: 87Sr/86Sr(i) = 0.704096–0.707805, 143Nd/144Nd(i) = 0.512012–0.512021 and for ?Nd270 the negative values from −5.27 to −5.44. They suggest to be generated within the lower crust during the emplacement of mantle-derived magmas that provided necessary heat to crustal partial melting.  相似文献   

18.
The isotopic composition of Nd in the water column from several western North Atlantic sites and formational areas for North Atlantic Deep Water shows extensive vertical structure at all locations. In regions where a thermocline is well-developed, large isotopic shifts (2 to 3 ϵ units) are observed across the base of the thermocline. Regions without a thermocline are characterized by much more gradual shifts in isotopic composition with depth. In general, the data reveal an excellent correlation between the Nd isotopic distribution in the western North Atlantic water column and the distribution of water masses identified from temperature and salinity characteristics. NADW, as identified from T-S properties, is also characterized by a well-defined isotopic composition having ϵNd(0) = −13.5 ± 0.5. This signature is associated with waters identified as NADW from high latitudes near formational areas in the Labrador Sea down to the equatorial region. The isotopic signature of NADW would appear to be formed by a blend of more negative waters originating in the Labrador Sea (ϵNd(0) < −18) and more positive waters originating in the overflows from the Norwegian and Greenland Seas (ϵNd(0) ≈ −8 to −10) and is consistent with classical theories on the formation of NADW. The isotopic signature of NADW is propagated southward to the equator where it is gradually being thinned out by mixing from above and below with more radiogenic Nd associated with northward-spreading Antarctic Intermediate and Bottom Waters. The preservation of the isotopic signature of NADW over these large distances indicate that the REE undergo extensive lateral transport. The isotopic composition of Nd is largely conservative over the time scales of mixing within the Atlantic in spite of the intrinsic nonconservative behavior of neodymium. Nd concentration gradients generally show surface waters to be depleted in Nd relative to deep waters, which must require vertical transport processes. However, isotopic differences in the water column preclude the local downward transport of REE from the surface into underlying deep waters as a simple explanation of the concentration gradient. The apparent decoupling of REE in NADW from overlying (local) surface waters and the increasing concentration with depth provide a conflict with simple vertical transport mechanisms that is not yet resolved.  相似文献   

19.
Several I- and A-type granite, syenite plutons and spatially associated, giant Fe-Ti-V deposit-bearing mafic-ultramafic layered intrusions occur in the Pan-Xi (Panzhihua-Xichang) area within the inner zone of the Emeishan large igneous province (ELIP). These complexes are interpreted to be related to the Emeishan mantle plume. We present LA-ICP-MS and SIMS zircon U-Pb ages and Hf-Nd isotopic compositions for the gabbros, syenites and granites from these complexes. The dating shows that the age of the felsic intrusive magmatism (256.2 ± 3.0-259.8 ± 1.6 Ma) is indistinguishable from that of the mafic intrusive magmatism (255.4 ± 3.1-259.5 ± 2.7 Ma) and represents the final phase of a continuous magmatic episode that lasted no more than 10 Myr. The upper gabbros in the mafic-ultramafic intrusions are generally more isotopically enriched (lower εNd and εHf) than the middle and lower gabbros, suggesting that the upper gabbros have experienced a higher level of crustal contamination than the lower gabbros. The significantly positive εHf(t) values of the A-type granites and syenites (+4.9 to +10.8) are higher than those of the upper gabbros of the associated mafic intrusion, which shows that they cannot be derived by fractional crystallization of these bodies. They are however identical to those of the mafic enclaves (+7.0 to +11.4) and middle and lower gabbros, implying that they are cogenetic. We suggest that they were generated by fractionation of large-volume, plume-related basaltic magmas that ponded deep in the crust. The deep-seated magma chamber erupted in two stages: the first near a density minimum in the basaltic fractionation trend and the second during the final stage of fractionation when the magma was a low density Fe-poor, Si-rich felsic magma. The basaltic magmas emplaced in the shallow-level magma chambers differentiated to form mafic-ultramafic layered intrusions accompanied by a small amount of crustal assimilation through roof melting. Evolved A-type granites (synenites and syenodiorites) were produced dominantly by crystallization in the deep crustal magma chamber. In contrast, the I-type granites have negative εNd(t) [−6.3 to −7.5] and εHf(t) [−1.3 to −6.7] values, with the Nd model ages () of 1.63−1.67 Ga and Hf model ages () of 1.56−1.58 Ga, suggesting that they were mainly derived from partial melting of Mesoproterozoic crust. In combination with previous studies, this study also shows that plume activity not only gave rise to reworking of ancient crust, but also significant growth of juvenile crust in the center of the ELIP.  相似文献   

20.
Fluorite can be used as a probe for the source of Sr and REE, as well as for the Sr and Nd isotope systematics of mineralizing solutions, allowing characterization of the composition, oxidation state and sources of the fluids. The 87Sr / 86Sr ratios in vein fluorite from the Santa Catarina Fluorite District, southern Brazil, are low (0.720 to 0.745) relative to those of the majority of host granites at the time of mineralization (90 Ma), but are similar to those of less abundant and less evolved Sr- and Ca-rich granites and plagioclases of the heterogeneous Pedras Grandes granite association. Major contributions of Sr from the unradiogenic Parana Basin rocks (87Sr / 86Sr90 Ma = 0.705 to 0.718) are unlikely, considering the radiogenic character of the lower 87Sr / 86Sr end-member in fluorite mixing lines. Estimated fluorite fluid partition coefficients (KdSr-Ca = 0.019 and DSr ≈ 600) indicate a Sr / Ca ratio in the fluorite-forming solution of 0.012, and Sr contents of 0.05 to 0.25 ppm, which are similar to those of present-day granitic geothermal waters. Initial Nd isotopic compositions of the vein fluorites (0.5120 to 0.512) are similar to those of the Pedras Grandes granites. The 143Nd / 144Nd90 Ma of the evolved granites of the Tabuleiro granite association, their accessory fluorites and the Parana Basin rocks are considerably more radiogenic (0.5120 to 0.5127) and these are thus considered to be unlikely sources of the fluids. The REE patterns of vein fluorites, normalized to upper continental crust, show a range of LREE-depleted patterns, with highly variable positive and negative Eu anomalies. The host Pedras Grandes granites show flat to slightly depleted UCC normalized LREE patterns with strong negative Eu anomalies. Depletion of the LREE in fluorites resulted from the mobility of HREE fluoride complexes during fluid migration. A REE fractionation model based on ionic potential ratios indicates that Eu3+ was stable during fluid migration and fluorite precipitation. The coexistence of pyrite and Eu3+ in the mineralizing fluids is consistent with low pH and oxygen fugacities near the hematite-magnetite buffer.  相似文献   

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