Distribution of yttrium and rare earths in Florida Bay sediments

The distribution of yttrium and rare earth elements (YREEs) in surface sediments was measured on samples collected from 40 stations in Florida Bay (June 2000 and February 2001). Florida Bay is the largest shallow carbonate estuary in South Florida with nearly pristine conditions. It receives fresh waters from some rivers and several canals from the Everglades which contribute rare earth elements and metals to the Bay. This paper is the first extensive study of YREEs in Florida Bay. Concentrations of YREEs (Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu) were determined by ICP-MS. The YREEs show a similar distribution pattern for the two months studied. The maximum concentrations were found in the western and north-central zones (near the Everglades) and the minimum concentrations were found in the south-central zone near the Florida Keys. The pattern of YREEs in Florida Bay sediments correlated strongly with those in the North American Shale Composite, indicating a dominant crustal source for these elements. However, the REE concentrations in Florida Bay sediments are depleted with respect to NASC. All REEs exhibited a strong correlation with Fe and Al from continental input and river runoff from the Everglades. The heavy REEs and Y showed a strong correlation with Al (R² > 0.84). The light and medium REEs showed a strong correlation with Fe (R² > 0.9). Correlations of all the YREEs with Mn were slightly lower (R²  0.7–0.75). The concentration of all the YREEs, Al and Fe are dependent on the bottom types and zones in the Bay, except Mn which decreases as it moves from the land to the sea.     

Time-series observation of dissolved inorganic carbon and nutrients in the northwestern North Pacific

Time-series measurements of dissolved inorganic carbon (DIC) and nutrient concentrations were conducted in the northwestern North Pacific from October 2002 to August 2004. Assuming that data obtained in different years represented time-series seasonal data for a single year, vertical distributions of DIC and nutrients showed large seasonal variabilities in the surface layer (∼100 m). Seasonal variabilities in normalized DIC (nDIC) and nitrate concentrations at the sea surface were estimated to be 81–113 μmol kg⁻¹ and 12.7–15.7 μmol kg⁻¹, respectively, in the Western Subarctic Gyre. The variability in nutrients between May and July was generally at least double that in other seasons. In the Western Subarctic Gyre, estimations based on statistical analyses revealed that seasonal new production was 39–61 gC m⁻² and tended to be higher in the southwestern regions or coastal regions. The seasonal new productions in the northwestern North Pacific were two or more times higher than in the North Pacific subtropical gyre and the northeastern North Pacific. It is likely that this difference is due to spatial variations in the concentrations of trace metals and the species of phytoplankton present. In addition, from estimations of surface pCO₂ it was verified that the Western Subarctic Gyre is a source of atmospheric CO₂ between February and May and a sink for CO₂ between July and October.     

Dissolved and labile particulate Zr,Hf, Nb,Ta, Mo and W in the western North Pacific Ocean

Dissolved and labile particulate Zr, Hf, Nb, Ta, Mo and W were determined at stations K1 (51°N, 165°E), K2 (47°N, 160°E), KNOT (44°N, 155°E) and 35N (35°N, 160°E) in the western North Pacific Ocean. A portion of seawater for dissolved species (D) was passed through a 0.2 μm Nuclepore filter and acidified to pH 2.2 with HCl and HF. A portion of seawater for acid-dissolvable species (AD) was acidified without filtration. Labile particulate (LP) species is defined as AD minus D, which represents a chemically labile fraction of particulate species. D-Zr, Hf and Ta increase with depth, Nb shows a slight depletion in surface water, whereas Mo and W have a conservative vertical profile. The concentration range of D-Zr, Hf, Nb, Ta and W is 31–275, 0.14–0.95, 4.0–7.2, 0.08–0.29 and 40–51 pmol kg⁻¹, respectively, whereas that of Mo is 97–105 nmol kg⁻¹. LP-species of Zr, Hf and Ta account for 10–14% of AD in average and increase up to 25% below 4000 m, whereas those for Mo and W are negligible. In contrast, LP-Nb shows maxima (up to 27%) in surface water. We also found that D-Zr/Hf, Nb/Ta and Mo/W mole ratios generally increase in the order continental crust < river water < coastal sea < open ocean.     

Dynamics of REE accumulation and fractionation in the subcolloidal fraction of bottom sediments in the Razdol’naya River–Amur Bay section,Sea of Japan

The REE contents (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu) are determined by atomic emission spectroscopy in the subcolloidal fraction of bottom sediments in the Razdol’naya River–Amur Bay section. The mean contents of lanthanides in soils and river bottom sediments (before the mixing zone) are calculated. The increase in REE content and the fractioning in the series from light to middle and heavy REE in sediments of different estuary zones (river, water mixing, and marine), with the latter related to flocculation, sorption on iron and manganese hydroxides, clay minerals (hydromica, smectites), and lifetime accumulation of marine plankton, are dtermined. Via extraction of 0.5 N sodium hydroxide solution, the content of lanthanides associated with humic substances of subcolloidal fraction from the Amur Bay sediments are determined: 1.3 to 8.2% of La; 1.1 to 11% of Ce; and 0.3 to 1.5 of Gd.     

Precise determination of the cerium isotopic compositions of surface seawater in the Northwest Pacific Ocean and Tokyo Bay

We succeeded in determining the Ce isotopic composition (¹³⁸Ce/¹⁴²Ce) in seawater with an error of 2σ_m = 0.3–0.7 of ε unit. In this study, 1000–3000 L of seawater samples were passed through MnO₂ fibers to concentrate Ce and Nd for precise measurement of their isotope ratios. Four surface seawater samples of the northwestern Pacific and a coastal sample in Tokyo Bay were analyzed. Most Ce isotope ratios in the surface water showed positive ε_Ce values (+ 0.8 to + 1.4) in the northwestern Pacific Ocean. These values indicate that Ce in the surface water originates from the continental crust preferentially over mantle-derived materials. We examined binary mixing model between the continental crust and mid-ocean ridge basalt. However the model could not explain both isotopic compositions and concentrations, which implies that the atmospheric input was a possible pathway for Ce into the ocean. A negative ε_Ce value was observed in Tokyo Bay, suggesting mantle-derived sources.     

Stable isotopic ratios of lead in surface waters of the Central Pacific

The geographic variation in the isotopic composition of lead in surface waters of the central Pacific provides new evidence of the global anthropogenic perturbation of the element's cycle. Ratios of ²⁰⁶Pb/²⁰⁷Pb decrease from 1.196 in the northern hemisphere (19°N, 158°W) to 1.176 in the southern hemisphere (15°S, 150°W). This decrease parallels the geographic variation in surface concentrations of soluble lead which decrease from 13 ng kg^?1 at the northern station to 4 ng kg^?1 at the southern station. Both the ²⁰⁶Pb/²⁰⁷Pb and the ²⁰⁶Pb/²⁰⁸Pb ratios of those waters fit between the isotopic ratios of Australian (Broken Hill) and North American (Mississippi Valley) leads which are the predominant sources of leads in anthropogenic emissions to the Pacific Ocean basin.     

Rare earth element fingerprints in Korean coastal bay sediments: Association with provenance discrimination

Rare earth elements (REEs: La-Lu) in surface sediments collected from the mouth and middle tidal flats of Gomso Bay, South Korea, in August 2011 and May 2012 were analyzed to investigate the fine-grained sediment provenance. The upper continental crust (UCC)-normalized light REEs (LREEs: La to Nd) were more enriched than the middle REEs (MREEs: Sm to Dy) and heavy REEs (HREEs: Ho to Lu), resulting in large (La/Yb)_UCC (1.9 ± 0.4) to (Gd/Yb)_UCC (1.4 ± 0.2) ratios. The monthly (La/Yb)_UCC values differed between the mouth and middle tidal flats due to deposition of fine-grained sediments that originated from distant rivers (the Geum and Yeongsan) and the Jujin Stream, located on the southern shore of the inner bay. We observed relative reductions in the (La/Yb)_UCC value and REE content in the sediments from the mouth of the bay compared with those from Jujin Stream sediments. Confined to the middle tidal flat around the KH Line of Jujin Stream, the sediments, most enriched in LREEs but depleted in Eu, were distributed in August as strong Jujin Stream runs. Here, we suggest that an increase in LREE/HREE and decrease in MREE/LREE ratios can be used as a proxy to identify the Jujin Stream provenance in mixed riverine sediments and to trace Jujin Stream sediments within the Gomso Bay tidal flat, especially in the summer rainy season.     

Rare earth elements in bottom sediments of major rivers around the Yellow Sea: implications for sediment provenance

Rare earth elements (REEs) of 91 fine-grained bottom sediment samples from five major rivers in Korea (the Han, Keum, and Yeongsan) and China (the Changjiang and Huanghe) were studied to investigate their potential as source indicator for Yellow Sea shelf sediments, this being the first synthetic report on REE trends for bottom sediments of these rivers. The results show distinct differences in REE contents and their upper continental crust (UCC)-normalized patterns: compared to heavy rare earth elements (HREEs), light rare earth elements (LREEs) are highly enriched in Korean river sediments, in contrast to Chinese river sediments that have a characteristic positive Eu anomaly. This phenomenon is observed also in primary source rocks within the river catchments. This suggests that source rock composition is the primary control on the REE signatures of these river sediments, due largely to variations in the levels of chlorite and monazite, which are more abundant in Korean bottom river sediments. Systematic variations in ΣLREE/ΣHREE ratios, and in (La/Yb)–(Gd/Yb)_UCC but also (La/Lu)–(La/Y)_UCC and (La/Y)–(Gd/Lu)_UCC relations have the greatest discriminatory power. These findings are consistent with, but considerably expand on the limited datasets available to date for suspended sediments. Evidently, the REE fingerprints of these river sediments can serve as a useful diagnostic tool for tracing the provenance of sediments in the Yellow Sea, and for reconstructing their dispersal patterns and the circulation system of the modern shelf, as well as the paleoenvironmental record of this and adjoining marginal seas.     

Seasonal and Interannual Variability in the Distribution of Surface Nutrients and Dissolved Inorganic Carbon in the Northern North Pacific: Influence of El Niño

The seasonal and interannual changes in surface nutrients, dissolved inorganic carbon (DIC) and total alkalinity (TA) were recorded in the North Pacific (30–54°N) from 1995 to 2001. This study focuses on the region north of the subarctic boundary (∼40°N) where there was extensive monthly coverage of surface properties. The nutrient cycles showed large interannual variations in the eastern and western subarctic gyres. In the Alaska Gyre the seasonal depletion of nitrate (ΔNO₃) increased from 8–14 μmol kg⁻¹ in 1995–1999 to 21.5 μmol kg⁻¹ in 2000. In the western subarctic the shifts were similar in amplitude but more frequent. The large ΔNO₃ levels were associated with high silicate depletions, indicating enhanced diatom production. The seasonal DIC:NO₃ drawdown ratios were elevated in the eastern and central subarctic due to calcification. In the western subarctic and the central Bering Sea calcification was significant only during 1997 and/or 1998, two El Ni?o years. Regional C/N stoichiometric molar ratios of 5.7 to 7.0 (>40°N) were determined based on the years with negligible or no calcification. The annual new production (NP_a) based on ΔNO₃ and these C/N ratios showed large interannual variations. NP_a was usually higher in the western than in the eastern subarctic. However, values of 84 gC m⁻²yr⁻¹ were found in the Alaska Gyre in 2000 which is similar to that in the most productive provinces of the northern North Pacific. There were also large increases in NP_a around the Alaska Peninsula in 1997 and 1998. Finally, the net removal of carbon by the biological pump was estimated as 0.72 Gt C yr⁻¹ in the North Pacific (>30°N). This revised version was published online in August 2006 with corrections to the Cover Date.     

Isotopic tracers for water masses in the coastal region of eastern Hokkaido

In this study we used two stable isotopes, δ¹³C and δ¹⁸O, for water mass classification in the coastal region off eastern Hokkaido. δ¹³C* values, which were corrected for the biological effect, and δ ¹⁸O values up to 300 m depth suggested that the isotopic character of the onshore and offshore water in the southern Okhotsk Sea, the Nemuro Strait and the western North Pacific could be explained by the mixing of three source waters: the Oyashio water (OYW), Soya Warm Current water (SWCW) and East Sakhalin Current water (ESCW). In summer, δ ¹³C*-δ ¹⁸O plots indicated mixing between SWCW from the southern Okhotsk Sea and OYW in the Pacific coast of southeastern Hokkaido, while temperature-salinity plots of the onshore water showed minimal difference from the offshore OYW. In winter, on the other hand, the mixed water of ESCW and OYW (or SWCW) appeared in the Pacific coastal region, distributed as cold, low salinity onshore water. Finally, we estimated mixing ratios of OYW, SWCW and ESCW in the coastal region of western North Pacific using their mean values of δ ¹³C* and δ ¹⁸O as endmembers. These results suggest seasonal and yearly changes of water mass combination en route from the southern Okhotsk Sea to the western North Pacific.     

Biogeochemical Variation in Dimethylsulfide, Phytoplankton Pigments and Heterotrophic Bacterial Production in the Subarctic North Pacific during Summer

Dimethylsulfide (DMS), chlorophyll a (Chl-a), accessory pigments (fucoxanthin, peridinin and 19-hexanoyloxyfucoxanthin), and bacterial production (BP) were measured in the surface layer (0–100 m) of the subarctic North Pacific, including the Bering Sea, during summer (14 July–5 September, 1997). In surface sewater, the concentrations of DMS and Chl-a varied widely from 1.3 to 13.2 nM (5.1 ± 3.0 nM, mean ± S.D., n = 48) and from 0.1 to 2.4 µg L^–1 (0.6 ± 0.6 µg L^–1, n = 24), respectively. In the subarctic North Pacific, DMS to Chl-a ratios (DMS/Chl-a) were higher on the eastern side than the western side (p < 0.0001). Below the euphotic zone, DMS/Chl-a ratios were law and the correlation between DMS and Chl-a was relatively strong (r ² = 0.700, n = 27, p < 0.0001). In the euphotic zone, DMS/Chl-a ratios were higher and the correlation between DMS and Chl-a was weak (r ² = 0.128, n = 50, p = 0.01). The wide variation in DMS/Chl-a ratios would be at least partially explained by the geographic variation in the taxonomic composition of phytoplankton, because of the negative correlation between DMS/Chl-a and fucoxanthin-to-Chl-a ratios (Fuc/Chl-a) (r ² = 0.476, n = 26, p = 0.0001). Furthermore, there was a positive correlation between DMS and BP (r ² = 0.380, n = 19, p = 0.005). This suggests that BP did not represent DMS and dimethylsulfoniopropionate (DMSP) removal by bacterial consumption but rather DMSP degradation to DMS by bacterial enzyme.     

Distribution of rare earth elements and neodymium isotopes in suspended particles of the tropical Atlantic Ocean (EUMELI site)

We analyzed the REE, Mn and Al concentrations and Nd isotopic ratios in marine suspensions collected on filters (0.65 μm porosity) with in situ pumping systems in the tropical northeastern Atlantic (20°N, 18–31°W). Previously we reported the same parameters on large sinking particles collected with moored sediment traps at the sites. Shale-normalized REE patterns of the filtered suspensions are characterized by a larger light REE (LREE) to heavy REE (HREE) enrichment compared to the trapped material and a Ce anomaly that evolves positively with depth. Depth profiles of REE/Al show maximum values at 50–100 m, where the Mn/Al ratio also reaches a maximum. The profile of the Nd isotopic ratios of the filtered suspensions shows variations similar to those of the seawater. These results suggest that the filtered suspensions preferentially scavenge the LREE, especially Ce, and that the particulate Mn oxides are potential REE carriers. The relationship between the Ce anomaly and the Ce/Al ratio demonstrates that the particulate Ce anomaly is formed by (1) the LREE adsorption onto the particulate Mn oxides in the surface water, (2) Ce(III) oxidation to insoluble Ce(IV)O₂ and (3) preferential desorption of strict trivalent REE from the Mn oxides in deep water. Estimated authigenic Nd contents, using Nd isotopic ratios, decrease with depth. This is consistent with the adsorption of the REE in surface water and their desorption in deep water, suggested by the Ce anomaly formation. All the results show that the suspended particles record more clearly the authigenic REE contribution than the trapped material does. The suspended matter plays a key role in the scavenging of particle-reactive elements.     

上新世/更新世之交太平洋经向翻转流演化

随着北半球冰盖的发育,全球气候环境发生了显著变化。太平洋经向翻转流（PMOC）对全球海洋热量分配和大气CO₂在深海的封存起举足轻重的作用,但是关于PMOC与北半球冰盖的形成之间的关系还欠缺研究。本文收集了太平洋海山富钴结壳的Nd同位素记录,通过对比不同区域Nd同位素记录的演化特征,分析风尘输入、水团演化等因素对Nd同位素记录的影响,探讨了太平洋经向翻转流演化及其与全球气候变化之间的关系,认为北太平洋深层水下沉的停滞和亚洲风尘输入增加可能是导致深层水Nd同位素从距今3～4 Ma开始降低的原因。同时,因北太平洋深层水下沉停滞,PMOC改组,使得更多的CO₂在深水封存,从而对全球气候变冷和北半球冰盖形成产生了积极的贡献。     

Distribution of nitrous oxide dissolved in water masses in the eastern subtropical North Pacific and its origin inferred from isotopomer analysis

N₂O concentration and its isotopomer ratios were measured over a wide area from San Diego to Honolulu in the eastern subtropical North Pacific (ESNP). Waters in the study area had an N₂O maximum (38.2–50.5 nmol kg^?1) at 600–1000 m depth, which is similar to the profiles obtained previously in other areas in the North Pacific. We separated the seawater into five water masses (two for the surface layer, two for the middle layer, and one for the deep layer) and deduced N₂O production–consumption mechanisms in each water body by use of N₂O isotopomer ratios. The results showed that the mechanisms differ slightly among water masses. In the “coastal” surface layer, N₂O is produced by nitrification (NH₂OH oxidation). In the “open ocean” surface layer, it is produced mainly by nitrifier denitrification and to a lesser extent by nitrification under substrate-limited conditions. In both “upwelling” and “open ocean” middle layers it is produced mainly by denitrification and to a lesser extent by nitrifier denitrification. It is also partly reduced. In the deep layer, it is produced predominantly by denitrification with partial reduction. In this way, isotopomers aid elucidation of production–consumption mechanisms of N₂O in the sea even though the mechanisms cannot always be ascertained.     

Export Production in the Equatorial and North Pacific Derived from Dissolved Oxygen, Nutrient and Carbon Data

A global ocean inverse model that includes the 3D ocean circulation as well as the production, sinking and remineralization of biogenic particulate matter is used to estimate the carbon export flux in the Pacific, north of 10°S. The model exploits the existing large datasets for hydrographic parameters, dissolved oxygen, nutrients and carbon, and determines optimal export production rates by fitting the model to the observed water column distributions by means of the “adjoint method”. In the model, the observations can be explained satisfactorily with an integrated carbon export production of about 3 Gt C yr⁻¹ (equivalent to 3⋅10¹⁵ gC yr⁻¹) for the considered zone of the Pacific Ocean. This amounts to about a third of the global ocean carbon export of 9.6 Gt C yr⁻¹ in the model. The highest export fluxes occur in the coastal upwelling region off northwestern America and in the tropical eastern Pacific. Due to the large surface area, the open-ocean, oligotrophic region in the central North Pacific also contributes significantly to the total North Pacific export flux (0.45 Gt C yr⁻¹), despite the rather small average flux densities in this region (13 gC m⁻²yr⁻¹). Model e-ratios (calculated here as ratios of model export production to primary production, as inferred from satellite observations) range from as high a value as 0.4 in the tropical Pacific to 0.17 in the oligotrophic central north Pacific. Model e-ratios in the northeastern Pacific upwelling regions amount to about 0.3 and are lower than previous estimates. This revised version was published online in July 2006 with corrections to the Cover Date.     

Major and trace element distributions in manganese nodules and micronodules as well as abyssal clay from the Clarion-Clipperton abyssal plain,Northeast Pacific

The contents of seven major components (TiO₂, Fe₂O₃, MgO, CaO, Na₂O, K₂O and P₂O₅) and 15 trace elements (Sc, V, Cr, Ni, Cu, Sr, Y, Zr, Ba, La, Ce, Nd, Eu, Yb and Th) were determined by ICP-AE spectrometry in 27 samples of manganese nodules, micronodules as well as abyssal clay collected by dredging from an area of nearly 1,9802 nautical miles in the central Clarion-Clipperton abyssal plain at a depth of about 4,500 m. Statistical analyses were used to compare among individual as well as pooled datasets, in addition to different indicators such as La/Th, Ni/Cu and LREE/HREE ratios for the Clarion-Clipperton samples, as well as between these and corresponding values for the upper continental crust (UCC), North America Shale Composite (NASC), and igneous Indian and Pacific Mid-Ocean Ridge Basalts (MORBs). The results show significant correlations between major components in the Clarion-Clipperton samples and Pacific Ocean MORB, whereas trace elements (excepting Ni and Cu) correlate better with the UCC and NASC. There is also depletion in LREEs, together with a Ce negative anomaly for all Clarion-Clipperton samples. The nodule, micronodule and abyssal clay datasets each reveal typical clusters of components such as P₂O₅ and Y, La, Nd, Eu, Tb, or Ni and Cu. Compared to abyssal clay, the nodule as well as micronodules show significant enrichment in Ni and Cu; nevertheless, an essentially constant Ni/Cu ratio indicates that all samples come from the sediment surface. The distributions of major components as well as trace elements for the Clarion-Clipperton samples present, to different degrees, characteristics common to both the upper continental crust and Mid-Ocean Ridge Basalt, strongly implying a hydrothermal origin, most probably from East Pacific Rise material transported by the Pacific North Equatorial Current.     

Oxygen minimum zones in the eastern tropical Atlantic and Pacific oceans

Within the eastern tropical oceans of the Atlantic and Pacific basin vast oxygen minimum zones (OMZ) exist in the depth range between 100 and 900 m. Minimum oxygen values are reached at 300–500 m depth which in the eastern Pacific become suboxic (dissolved oxygen content <4.5 μmol kg⁻¹) with dissolved oxygen concentration of less than 1 μmol kg⁻¹. The OMZ of the eastern Atlantic is not suboxic and has relatively high oxygen minimum values of about 17 μmol kg⁻¹ in the South Atlantic and more than 40 μmol kg⁻¹ in the North Atlantic. About 20 (40%) of the North Pacific volume is occupied by an OMZ when using 45 μmol kg⁻¹ (or 90 μmol kg⁻¹, respectively) as an upper bound for OMZ oxygen concentration for ocean densities lighter than σ_θ < 27.2 kg m⁻³. The relative volumes reduce to less than half for the South Pacific (7% and 13%, respectively). The abundance of OMZs are considerably smaller (1% and 7%) for the South Atlantic and only 0% and 5% for the North Atlantic. Thermal domes characterized by upward displacements of isotherms located in the northeastern Pacific and Atlantic and in the southeastern Atlantic are co-located with the centres of the OMZs. They seem not to be directly involved in the generation of the OMZs.OMZs are a consequence of a combination of weak ocean ventilation, which supplies oxygen, and respiration, which consumes oxygen. Oxygen consumption can be approximated by the apparent oxygen utilization (AOU). However, AOU scaled with an appropriate consumption rate (aOUR) gives a time, the oxygen age. Here we derive oxygen ages using climatological AOU data and an empirical estimate of aOUR. Averaging oxygen ages for main thermocline isopycnals of the Atlantic and Pacific Ocean exhibit an exponential increase with density without an obvious signature of the OMZs. Oxygen supply originates from a surface outcrop area and can also be approximated by the turn-over time, the ratio of ocean volume to ventilating flux. The turn-over time corresponds well to the average oxygen ages for the well ventilated waters. However, in the density ranges of the suboxic OMZs the turn-over time substantially increases. This indicates that reduced ventilation in the outcrop is directly related to the existence of suboxic OMZs, but they are not obviously related to enhanced consumption indicated by the oxygen ages. The turn-over time suggests that the lower thermocline of the North Atlantic would be suboxic but at present this is compensated by the import of water from the well ventilated South Atlantic. The turn-over time approach itself is independent of details of ocean transport pathways. Instead the geographical location of the OMZ is to first order determined by: (i) the patterns of upwelling, either through Ekman or equatorial divergence, (ii) the regions of general sluggish horizontal transport at the eastern boundaries, and (iii) to a lesser extent to regions with high productivity as indicated through ocean colour data.     

白垩纪以来太平洋上地幔组成和温度变化

The geological evolution of the Earth during the mid-Cretaceous were shown to be anomalous, e.g., the pause of the geomagnetic field, the global sea level rise, and increased intra-plate volcanic activities, which could be attributed to deep mantle processes. As the anomalous volcanic activities occurred mainly in the Cretaceous Pacific, here we use basalt chemical compositions from the oceanic drilling(DSDP/ODP/IODP) sites to investigate their mantle sources and melting conditions. Based on locations relative to the Pacific plateaus, we classified these sites as oceanic plateau basalts, normal mid-ocean ridge basalts, and near-plateau seafloor basalts. This study shows that those normal mid-ocean ridge basalts formed during mid-Cretaceous are broadly similar in average Na8, La/Sm and Sm/Yb ratios and Sr-Nd isotopic compositions to modern Pacific spreading ridge(the East Pacific Rise). The Ontong Java plateau(125–90 Ma) basalts have distinctly lower Na8 and143Nd/144 Nd, and higher La/Sm and 87Sr/86 Sr than normal seafloor basalts, whereas those for the near-plateau seafloor basalts are similar to the plateau basalts, indicating influences from the Ontong Java mantle source. The super mantle plume activity that might have formed the Ontong Java plateau influenced the mantle source of the simultaneously formed large areas of seafloor basalts. Based on the chemical data from normal seafloor basalts, I propose that the mantle compositions and melting conditions of the normal mid-ocean ridges during the Cretaceous are similar to the fast spreading East Pacific Rise. Slight variations of mid-Cretaceous normal seafloor basalts in melting conditions could be related to the local mantle source and spreading rate.     

Interannual variation of rare earth element abundances in corals from northern coast of the South China Sea and its relation with sea-level change and human activities

Here we present interannual rare earth element (REE) records spanning the last two decades of the 20th century in two living Porites corals, collected from Longwan Bay, close to the estuarine zones off Wanquan River of Hainan Island and Hong Kong off the Pearl River Delta of Guangdong Province in the northern South China Sea. The results show that both coral REE contents (0.5-40 ng g?1 in Longwan Bay and 2-250 ng g?1 in Hong Kong for La-Lu) are characterized with a declining trend, which are significantly negative correlated with regional sea-level rise (9.4 mm a?1) from 1981 to 1996 in Longwan Bay, 13.7 mm a?1 from 1991 to 2001 in Hong Kong). The REE features are proposed to be resulted from seawater intrusion into the estuaries in response to contemporary sea-level rise. However, the tendency for the coral Er/Nd time series at Hong Kong site is absent and there is no significant relation between Er/Nd and total REEs as found for the coral at Longwan Bay site. The observations are likely attributed to changes of the water discharge and sediment load of Pearl River, which have been significantly affected by intense human activities, such as the construction of dams/reservoirs and riverbed sediment mining, in past decades. The riverine sediment load/discharge ratio of the Pearl River decreased sharply with a rate of 0.02 kg m?3 a?1, which could make significant contribution to the declining trend of coral REE. We propose that coastal corals in Longwan Bay and similar unexplored sites with little influences of river discharge and anthropogenic disruption are ideal candidates to investigate the influence of sea-level change on seawater/coral REE.     

Silver in Tokyo Bay estuarine waters and Japanese rivers

Dissolved and particulate concentrations of silver in Tokyo Bay estuarine waters and Japanese rivers were determined in this study. The dissolved silver concentrations in the surface water of Tokyo Bay range from 5.9 to 15.1 pmol kg⁻¹, which is comparable to those in the surface water of the Japan Sea, but two or three times higher than those in the surface water of the open ocean. However, elevated concentrations of dissolved silver are not found in Tokyo Bay compared with those in other highly urbanized estuaries, such as San Francisco Bay (20∼243 pmol kg⁻¹). In the Tokyo Bay estuary, silver typically exhibits non-conservative mixing behavior, which is a common feature in the other estuaries reported previously. Dissolved silver concentrations decrease with salinity from the rivers to the mouth of Tokyo Bay. Silver is efficiently scavenged by suspended particulates, as evidenced by the high conditional distribution coefficients for silver throughout the estuary (log K_d > 5.0 ± 0.6). The silver fluxes into Tokyo Bay via inflowing rivers and atmospheric deposition were estimated as 83 kg y⁻¹ and 15 kg y⁻¹, respectively. A simple budget calculation shows that the silver supplied from rivers and atmosphere must be rapidly scavenged within the Tokyo Bay estuary.