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1.
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   

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.
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   

4.
The distribution of neodymium isotopes in Arctic Ocean basins   总被引：1，自引：0，他引：1  
Nd concentration and isotope data have been obtained for the Canada, Amundsen, and Makarov Basins of the Arctic Ocean. A pattern of high Nd concentrations (up to 58 pM) at shallow depths is seen throughout the Arctic, and is distinct from that generally seen in other oceans where surface waters are relatively depleted. A range of isotopic variations across the Arctic and within individual depth profiles reflects the different sources of waters. The dominant source of water, and so Nd, is the Atlantic Ocean, with lesser contributions from the Pacific and Arctic Rivers. Radiogenic isotope Nd signatures (up to εNd = −6.5) can be traced in Pacific water flowing into the Canada Basin. Waters from rivers draining older terrains provide very unradiogenic Nd (down to εNd = −14.2) that can be traced in surface waters across much of the Eurasian Basin. A distinct feature of the Arctic is the general influence of the shelves on the Nd concentrations of waters flowing into the basins, either from the Pacific across the Chukchi Sea, or from across the extensive Siberian shelves. Water-shelf interaction results in an increase in Nd concentration without significant changes in salinity in essentially all waters in the Arctic, through processes that are not yet well understood. In estuarine regions other processes modify the Nd signal of freshwater components supplied into the Arctic Basin, and possibly also contribute to sedimentary Nd that may be subsequently involved in sediment-water interactions. Mixing relationships indicate that in estuaries, Nd is removed from major river waters to different degrees. Deep waters in the Arctic are higher in Nd than the inflowing Atlantic waters, apparently through enrichments of waters on the shelves that are involved in ventilating the deep basins. These enrichments generally have not resulted in major shifts in the isotopic compositions of the deep waters in the Makarov Basin (εNd ∼ −10.5), but have created distinctive Nd isotope signatures that were found near the margin of the Canada Basin (with εNd ∼ −9.0). The deep waters of the Amundsen Basin are also distinct from the Atlantic waters (with εNd = −12.3), indicating that there has been limited inflow from the adjacent Makarov Basin through the Lomonosov Ridge.  相似文献   

5.
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   

6.
A study of lateritic soils and samples of ground and river waters was carried out in the Nsimi-Zoetele, a tropical watershed in the southern Cameroon. The Nd isotopic compositions and concentrations of Nd and Sm were determined. It was found that the Nd isotopic composition of the river waters was much more radiogenic than the parent rocks, and that the Nd in the waters is not homogeneous but is carried by different dissolved and complexed components that are not isotopically homogenized. The soil profile shows a regular increase in εNd going from the parent rock (εNd = −36) to εNd = −18 near the top of the profile. The Nd transported in the river is thus not representative of the parent rock but reflects the results of differential weathering of constituent minerals and the redeposition of REE in phosphates and a significant contribution of radiogenic Nd from dust. The concentration of Nd in the river water is far above that found in temperate climate rivers and thus this type of tropical river may play a dominant role in the marine Nd and REE budget. It is suggested that the correlation of REE with DOC is related to DOC fixing some dissolved REE but that the REE in solution is governed by other mechanisms. No major shifts were found in Sm/Nd; however, a regular progression from the parent rock through the lateritic profile was found. The upper laterite profile shows large, almost uniform depletions in all REE below Tb and enrichment above. Complementary behavior was found in the lower part of the section. The concentration of Nd relative to the immobile elements Zr and Ti in the laterite is depleted by a factor of ∼10. Th, Nd and Sm are enriched in the lowest zone sampled and must reflect redeposition of REE from the upper part of the weathering section and is associated with phosphate formation. It is concluded that the soil evolution involves both differential dissolution of primary phases from the parent rock, significant to major input of REE from atmospheric dust from other regions, and the formation of diagenetic phases, particularly phosphates.  相似文献   

7.
The behavior of dissolved Hf in the marine environment is not well understood due to the lack of direct seawater measurements of Hf isotopes and the limited number of Hf isotope time-series obtained from ferromanganese crusts. In order to place better constraints on input sources and develop further applications, a combined Nd-Hf isotope time-series study of five Pacific ferromanganese crusts was carried out. The samples cover the past 38 Myr and their locations range from sites at the margin of the ocean to remote areas, sites from previously unstudied North and South Pacific areas, and water depths corresponding to deep and bottom waters.For most of the samples a broad coupling of Nd and Hf isotopes is observed. In the Equatorial Pacific εNd and εHf both decrease with water depth. Similarly, εNd and εHf both increase from the South to the North Pacific. These data indicate that the Hf isotopic composition is, in general terms, a suitable tracer for ocean circulation, since inflow and progressive admixture of bottom water is clearly identifiable.The time-series data indicate that inputs and outputs have been balanced throughout much of the late Cenozoic. A simple box model can constrain the relative importance of potential input sources to the North Pacific. Assuming steady state, the model implies significant contributions of radiogenic Nd and Hf from young circum-Pacific arcs and a subordinate role of dust inputs from the Asian continent for the dissolved Nd and Hf budget of the North Pacific.Some changes in ocean circulation that are clearly recognizable in Nd isotopes do not appear to be reflected by Hf isotopic compositions. At two locations within the Pacific Ocean a decoupling of Nd and Hf isotopes is found, indicating limited potential for Hf isotopes as a stand-alone oceanographic tracer and providing evidence of additional local processes that govern the Hf isotopic composition of deep water masses. In the case of the Southwest Pacific there is evidence that decoupling may have been the result of changes in weathering style related to the buildup of Antarctic glaciation.  相似文献   

8.
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   

9.
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   

10.
基于AMS14C测年、有机碳、氮含量及其同位素等指标分析,探讨了冲绳海槽中南部OKT-3孔末次冰消期以来沉积物有机质来源及其对古海洋环境演化的响应。结果显示,OKT-3孔沉积物中有机质主要由中国大陆和中国台湾等陆源有机质,以及海洋自生有机质组成。末次冰消期至全新世晚期（17.3~4 ka B.P.）,中国大陆源有机质贡献逐渐下降,中国台湾源有机质贡献逐渐上升,表明海平面变化、黑潮变动是该阶段有机质来源的主要控制因素。4~1.5 ka期间,陆源有机质供给变化趋势与黑潮变动不一致,表明该时期陆源输入非黑潮单一控制,还可能受季风降雨等变化影响。值得注意的是,OKT-3孔海源有机质贡献在B-A和PB时期高、YD时期低,与北太平洋地区的生产力变化相似,反映了北太平洋中层水（NPIW）对海水表层生产力的控制作用,NPIW是连通冲绳海槽与北太平洋的重要纽带。  相似文献   

11.
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   

12.
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   

13.
Trace metal clean techniques were used to sample Hawaii Ocean Time-series (HOT) station ALOHA on seven occasions between November 1998 and October 2002. On three occasions, full water-column profile samples were obtained; on the other four occasions, surface and near-surface euphotic zone profiles were obtained. Together with three other published samplings, this site may have been monitored for “dissolved” (≤0.4 or ≤0.2 μm) Fe more frequently than any other open ocean site in the world.Low Fe concentrations (<0.1 nmol kg−1) are seen in the lower euphotic zone, and Fe concentrations increase to a maximum in intermediate waters. In the deepwaters (>2500 m), the concentrations we observe (0.4-0.5 nmol kg−1) are significantly lower than some other deep North Pacific stations but are similar to values that have been reported for a station 350 miles to the northeast. We attribute these low deepwater values to transport of low-Fe Antarctic Bottom Water into the basin and a balance between Fe regeneration and scavenging in the deep water. Near-surface waters have higher Fe levels than observed in the lower euphotic zone. Significant temporal variability is seen in near-surface Fe concentrations (ranging from 0.2-0.7 nmol kg−1); we attribute these surface Fe fluctuations to variable dust deposition, biological uptake, and changes in the mixed layer depth. This variability could occur only if the surface layer Fe residence time is less than a few years, and based on that constraint, it appears that a higher percentage of the total Fe must be released from North Pacific aerosols compared to North Atlantic aerosols. Surprisingly, significant temporal variability and high particulate Fe concentrations are observed for intermediate waters (1000-1500 m). These features are seen in the depth interval where high δ3He from the nearby Loihi Seamount hydrothermal fields has been observed; the total Fe/3He ratio implies that the hydrothermal vents are the source of the high and variable Fe.The vertical profile of Mn at ALOHA qualitatively resembles other North Pacific Mn profiles with surface and intermediate water maxima, but there are some significant quantitative differences from other reported profiles. The ≤0.4 μm Mn concentration is highest near the surface, decreases sharply in the upper 500 m, then shows an intermediate water maximum at 800 m and then decreases in the deepest waters; these concentrations are higher than observed at a station 350 miles to the northeast that shows similar vertical variations. It appears that there is a significant Mn gradient (throughout the water column) from HOT towards the northeast.Compared to the first valid oceanic Pb data for samples collected in 1976, Pb at ALOHA in 1997-1999 shows decreases in surface waters and waters shallower than 200 m. Pb concentrations in central North Pacific surface waters have decreased by a factor of 2 during the past 25 yr (from ∼65 to ∼30 pmol kg−1); surface water Pb concentrations in the central North Atlantic and central North Pacific are now comparable. We attribute the surface water Pb decrease to the elimination of leaded gasoline in Japan and to some extent by the U.S. and Canada. We attribute most of the remaining Pb in Pacific surface waters to Asian emissions, more likely due to high-temperature industrial activities such as coal burning rather than to leaded gasoline consumption. A 3-year mixed-layer time series from the nearby HALE-ALOHA mooring site (1997-1999) shows that there is an annual cycle in Pb with concentrations ∼20% higher in winter months; this rise may be created by downward mixing of the winter mixed layer into the steep gradient of higher Pb in the upper thermocline (Pb concentrations double between the surface and 200 m). From 200 m to the bottom, Pb concentrations decrease to levels of 5-9 pmol kg−1 near the bottom; for most of the water column, thermocline and deepwater Pb concentrations do not appear to have changed significantly during the 23-yr interval.  相似文献   

14.
The Pb, Sr and Nd isotopic compositions of biomonitors (lichen, moss, bark) and soil litter from different regions in the Rhine valley, as well as of <0.45 μm particles separated out of ice of the Rhône and Oberaar glaciers and lichens from the Swiss Central Alps, have been determined in order to deduce the natural baseline of the atmospheric isotopic compositions of these regions, which are suggested to be close to the isotopic compositions of the corresponding basement rocks or soils at the same sites. 206Pb/207Pb and 87Sr/86Sr isotope ratios are positively correlated. Most polluted samples from traffic-rich urban environments have the least radiogenic Pb and Sr isotopic compositions with 206Pb/207Pb and 87Sr/86Sr ratios of 1.11 and 0.7094, respectively. These ratios are very different from those of the atmospheric baseline for the Vosges mountains and the Rhine valley (206Pb/207Pb: 1.158–1.167; 87Sr/86Sr: 0.719–0.725; εNd: −7.5 to −10.1). However, this study indicates that the baseline of the atmospheric natural Pb and Sr isotopic compositions is affected by anthropogenic (traffic, industrial and urban) emissions even in remote areas. Lichen samples from below the Rhône and Oberaar glaciers reflect the baseline composition close to the Grimsel pass in the Central Swiss Alps (87Sr/86Sr: 0.714 − 0.716; εNd: −3.6 to −8.1). The 143Nd/144Nd isotope ratios are highly variable (8ε units) and it is suggested that the variation of the 143Nd/144Nd is controlled by wet deposition and aerosols originating from the regional natural and industrial urban environments and from more distant regions like the Sahara in North Africa. The least anthropogenetically affected samples collected in remote areas have isotopic compositions closest to those of the corresponding granitoid basement rocks.  相似文献   

15.
Main spawning and nursery grounds of the Pacific Sardine are formed in the coastal boundary regions of the Kuroshio S of Kyushu and S of Honshu, respectively. Numerical experiments on the transport and dispersion of particles in and neighbouring areas of the Kuroshio were done to investigate the transport process of the fish eggs and larvae from the spawning ground to the downstream nursery ground. Surface currents measured with GEK in the past were averaged for both paths with and without large meanders of the Kuroshio in the S of Honshu and used as the data basis. Particles were released in the Kuroshio SE of Kyushu. The results show that the transport rate of them into the S coastal waters of Honshu during large meandered path is larger than the rate during the straight path period. However, recruitment rates of the Pacific Sardine in the S coastal waters of Honshu decreases during the large meander periods of the Kuroshio path. This inverse correlation is considered to be caused by the poorer food environment strongly influenced by the intrusion of the Kuroshio water.  相似文献   

16.
Isotopic analyses of Nd and Sr on individual microtektites and a bulk microtektite sample from Barbados show them to have a very well defined isotopic composition. These data plot on an εSrεNd diagram precisely within the narrow field determined by North American tektites (εSr ≈ 111; εNd ≈ ?6.2). They yield an Nd model age of 0.6 AE. These results show that the microtektites from the Oceanic beds of late Eocene age are derived from the same target as the North American tektites and should be associated with the same event. Samples of the deep sea sediments in which the Barbados microtektites occur are found to have isotopic signatures which appear to reflect ambient sea water and detrital sediments. They cannot be the source of Sr or Nd in the tektites. Following the arguments of Shaw and Wasserburg (1982) we conclude that the target area which produced the North American tektite field was composed of sediments (Eocambrian or younger) derived from very late Precambrian crust. Glass beads from Lake Wanapitei Crater are isotopically different from all other tektites (εSr ≈ 960; εNd ≈ ?31.4) and cannot be related to the North American tektites.  相似文献   

17.
Isotopic characteristics of river sediments on the Tibetan Plateau   总被引：1，自引：0，他引：1  
We systematically collected 40 modern clastic sediment samples from rivers in different tectonic units of the Tibetan Plateau and measured their Sr–Nd isotopic compositions. The isotopic characteristics provide insight into the controversial paleo-tectonic affinity of terranes of the Tibetan Plateau and the provenance of Songpan–Ganzi flysch complex. The Qilian Terrane and Himalaya Terrane have more negative εNd(0) values (from ? 14.3 to ? 11.8 and from ? 20.64 to ? 13.26, respectively) and high 87Sr/86Sr values (from 0.719674 to 0.738818 and from 0.721020 to 0.824959, respectively), reflecting old and mature continental crust origin of these two terranes. The southern Lhasa Terrane is more radiogenic in εNd(0) values (from ? 8.82 to ? 3.8) and low in 87Sr/86Sr values (from 0.711504 to 0.719489), implying the combined impact of the Neo-Tethys mantle and Himalaya old continental crust. Sr–Nd isotopic compositions of the Qilian Terrane are similar to those in the Yangtze Craton, indicating that the Qilian Terrane was probably separated from the Yangtze Craton. Sr–Nd isotopic characteristics of the Songpan–Ganzi Terrane are similar to the Yangtze Craton and are remarkably different to those in the North China Craton, eastern Kunlun–Qaidam and the central Qiangtang metamorphic belt, implying that the widely distributed flysch complex of the Songpan–Ganzi Terrane was sourced from the Yangtze Craton.  相似文献   

18.
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   

19.
The present-day North Chilean Coastal Cordillera between 18°30′S and 22°S records an important part of the magmatic evolution of the Central Andes during the Jurassic. Calc-alkaline to subordinate tholeiitic members from four rock groups with biostratigraphically constrained age display incompatible element pattern characteristic of convergent plate-margin volcanism, whereas alkaline basalts of one group occurring in the Precordillera show OIB-type trace element signatures. The correlation of biostratigraphic ages, regional distribution, and composition of the volcanic rocks provides a basis for the discussion on geochemical evolution and isotope ratios.Major and trace element distributions of the volcanic rocks indicate their derivation from mantle-derived melts. LILE and LREE enrichments in calc-alkaline basaltic andesites to dacites and some of the tholeiites hint at the involvement of hydrous fluids during melting and mobile element transport processes. A part of the Early Bajocian to ?Lower Jurassic and Oxfordian andesites and dacites are adakite-like rocks with a substantial participation of slab melt and are characterized by high Sr/Y ratios and low HREE contents. The Middle Jurassic tholeiitic and calc-alkaline basalts and basaltic andesites have been transported and partly stored within a system of deep-seated feeder fissures and crustal strike-slip faults before eruption.The isotopic composition of Sr (87Sr/86Sri=0.7032-0.7056) and Nd (εNdi=2.2-7.1) of the Jurassic volcanic rocks mostly fall in the range characteristic for mantle melts although some crustal components may have been involved. A few samples show slightly more radiogenic Sr isotopic composition, which is probably due to interaction with ancient sea-water. The Pb isotopic composition of the arc rocks is uncoupled from the isotopic composition of Sr and Nd and is dominated by the crustal component. Since the Cretaceous and Modern arc volcanic rocks show Pb isotopic compositions that can be largely explained by in situ Pb isotope growth of Jurassic arc volcanic rocks, we argue that the various Andean arc systems between 18°30′S and 22°S formed on the same type of basement.Most of the investigated samples have high Ba, Zr, and Th concentrations compared to island arc mafic volcanic rocks. About 20% of the Jurassic arc volcanics comprise of dacitic to rhyolitic rocks. These characteristics combined with the Pb isotopic composition that shows the influence of a Palaeozoic (or partly older) basement point to a continental margin setting for the North Chilean Jurassic arc. The distribution of the magmatic rocks throughout time, their textures, and the character of intercalated sedimentary rocks reflect westward movement of the magma sources and of the arc/back-arc boundary relative to the current coast line during the Early Bajocian on a broad front between 19°30′ and 21°S.  相似文献   

20.
The magma sources for granitic intrusions related to the Mesozoic White Mountain magma series in northern New England, USA, are addressed relying principally upon Nd isotopes. Many of these anorogenic complexes lack significant volumes of exposed mafic lithologies and have been suspected of representing crustal melts. Sm–Nd and Rb–Sr isotope systematics are used to evaluate magma sources for 18 felsic plutons with ages ranging from about 120 to 230 Ma. The possibility of crustal sources is further examined with analyses of representative older crust including Paleozoic granitoids which serve as probes of the lower crust in the region. Multiple samples from two representative intrusions are used to address intrapluton initial isotopic heterogeneities and document significant yet restricted variations (<1 in Nd). Overall, Mesozoic granite plutons range in Nd [T] from +4.2 to -2.3, with most +2 to 0, and in initial 87Sr/86Sr from 0.7031 to 0.709. The isotopic variations are roughly inversely correlated but are not obviously related to geologic, geographic, or age differences. Older igneous and metamorphic crust of the region has much lower Nd isotope ratios with the most radiogenic Paleozoic granitoid at Nd [180 Ma] of -2.8. These data suggest mid-Proterozoic separation of the crust in central northern New England. Moreover, the bulk of the Mesozoic granites cannot be explained as crustal melts but must have large mantle components. The ranges of Nd and Sr isotopes are attributed to incorporation of crust by magmas derived from midly depleted mantle sources. Crustal input may reflect either magma mixing of crustal and mantle melts or crustal assimilation which is the favored interpretation. The results indicate production of anorogenic granites from mantle-derived mafic magmas.  相似文献   

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