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1.
M. Lutfi Firdaus Kazuhiro Norisuye Yusuke Nakagawa Seiji Nakatsuka Yoshiki Sohrin 《Journal of Oceanography》2008,64(2):247-257
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. 相似文献
2.
A chemoreduction-purge-and-trap gas chromatographic method has been developed for the determination of trace dimethylsulfoxide (DMSO) in seawater. In the analysis procedure, DMSO was first reduced to dimethylsufide (DMS) by sodium borohydride and then the produced DMS was analyzed using the purge-and-trap technique coupled with gas chromatographic separation and flame photometric detection. Under the optimum conditions, 97% DMSO was reduced in the standard solution samples with a standard deviation of 5% (n=5). The detection limit of DMSO was 2.7 pmol of sulfur, corresponding to a concentration of 0.75 nmol/L for a 40 ml sample. This method was applied to determine the dissolved DMSO (DMSOd) and particulate DMSO (DMSOp) concentrations in the surface seawater of the Jiaozhou Bay, and the results showed that the DMSOd and DMSOp concentrations varied from 16.8 to 921.1 nmol/L (mean:165.2 nmol/L) and from 8.0 to 162.4 nmol/L (mean:57.7 nmol/L), respectively. The high concentrations of DMSOp were generally found in productive regions. Consequently, a significant correlation was found between the concentrations of DMSOp and chlorophyll a, suggesting that phytoplankton biomass might play an important role in controlling the distribution of DMSOp in the bay. Moreover, in the study area, the concentrations of DMSOd were significantly correlated with the levels of DMS, implying that the production of DMSOd is mainly via photochemical and biological oxidation of DMS. 相似文献
3.
H.A. van der Sloot D. Hoede J. Wijkstra J.C. Duinker R.F. Nolting 《Estuarine, Coastal and Shelf Science》1985,21(5):633-651
Oxy-anionic species of V, As, Se, Mo, Sb, Te and W were measured in solution and suspension in samples obtained during several cruises in the Dutch Wadden Sea, the offshore region of the Southern Bight (North Sea) and in the estuaries of the Rhine and Scheldt. Dissolved concentrations at salinities above 34·5 × 10?3 ( = 34·5%. S) agreed generally well with published open ocean values. It is suggested that Se speciation differs from the open ocean.In the Wadden Sea, concentrations of V, Se, Mo and Sb were linearly related to salinity (10–35 × 10?3). The good agreement between measured and extrapolated values at a salinity of 0·5 × 10?3 suggests conservative behaviour in the Rhine estuary (with residence time of freshwater in the order of a few days).Dissolved concentration vs. salinity plots in the Scheldt estuary (residence time 2–3 months) showed pronounced minima and maxima. These occurred in the low or medium salinity range for V, As and Sb. Linear behaviour was observed for Se and Mo (in some cases, relatively large differences between cruises were detected). Deviations from linearity in the plots are interpreted in terms of thermodynamic equilibrium conditions involving species with different solubilities (V), local input from land (As, Se, Sb, Te) and removal from solution (As), probably through coprecipitation with Fe(OH)3.In the offshore samples, the contributions of particulate forms to the total element concentrations were small (<15%). At higher SPM concentrations (about 30 mg dm?3), this percentage remained small for Se, Mo and Sb (<15%); it was substantial for V and As (25–50%). 相似文献
4.
《Marine Chemistry》2007,103(1-2):122-130
Phosphomolybdenum blue (PMB) paired with cetyltrimethylammonium bromide (CTAB) can be extracted using a solid phase extraction technique on C18 sorbent. Based on this, a novel on-line solid phase extraction method coupled with flow injection (FI) analysis and colorimetric detection has been established to determine nanomolar level orthophosphate in seawater. A stopped flow technique was employed to assure the complete formation of the PMB–CTAB compound, which was sequentially extracted on an in-line Sep-Pak C18 cartridge. The adsorbed PMB–CTAB can be rapidly eluted by 0.56 mol/L H2SO4 in ethanol, and determined with a spectrophotometer at 700 nm. Experimental parameters, including reaction temperature, sample loading flow rate, stopped time and eluting flow rate, were optimized throughout the experiments based on univariate experimental design. The results show that reaction temperature and stopped time were the major factors affecting the formation of PMB–CTAB. Silicate concentration up to 5000 times higher than that of orthophosphate would not interfere with the determination of orthophosphate. Using artificial seawater with salinity of 35 as a matrix under the optimized conditions, the standard curve shows a linear range between 3.2 and 48.5 nmol/L, and the recovery and the detection limit of the proposed method are 96.4% and 1.57 nmol/L, respectively. The relative standard deviation (RSD) (n = 8), which was determined daily for 8 days, was 4.52% for the artificial seawater at a concentration of 32.4 nmol/L orthophosphate. Two typical seawater samples were analyzed using both the proposed method and the MAGnesium hydroxide-Induced Coprecipitation (MAGIC) method. The results of the two methods show no significant difference using the t test. Compared to the MAGIC method, the proposed method has the advantage of being more sensitive, faster, sample saving and easy for on-line analysis. 相似文献
5.
A thorough understanding of the biogeochemical cycling of trace metals in the ocean is crucial because of the important role these elements play in regulating metabolism in marine biotas and thus, the climate. However, a precise and accurate analysis of trace metals in seawater is difficult because they are present at extremely low concentrations in a high salt matrix. In this study, we report an analytical method for the preconcentration and separation of six trace metals, Fe, Ni, Cu, Zn, Cd and Pb, in seawater using a seaFAST automatic solid-phase extraction device, analysis by a triple quadrupole collision/reaction technique with inductively coupled plasma mass spectrometry (ICP-MS), and quantification by the isotope dilution technique. A small volume (10 mL) of seawater sample was mixed with a multi-element isotope spike and subjected to seaFAST procedures. The preconcentrate solution was then analyzed using the optimized collision/reaction cell mode of ICP-MS, with NH3 gas for Fe and Cd with a flow rate of 0.22 mL/min and He for Ni, Cu, Zn and Pb with a flow rate of 4.0 mL/min. The procedure blanks were 130 pmol/L, 3.0 pmol/L, 6.8 pmol/L, 37 pmol/L, 0.29 pmol/L and 0.42 pmol/L, for Fe, Ni, Cu, Zn, Cd and Pb, respectively. The method was validated using five reference materials (SLRs-6, SLEW-3, CASS-6, NASS-7 and GEOTRACE-GSC), and our results were consistent with the consensus values. The method was further validated by measuring full-water-column seawater samples from the subtropical Northwest Pacific Ocean, and our results demonstrated good oceanic consistency. 相似文献
6.
The distribution of aluminum (Al) in seawater has been investigated in the continental slope and the Okinawa Trough areas
of the East China Sea, which is one of the marginal seas in the western North Pacific Ocean. Aluminum concentration in waters
over the slope and the Trough ranged from 5.6 to 25 nmol/kg in the surface layer (0–100 m), and had a minima of 1.1 nmol/kg
between 400 and 500 m depth and ranged from 1.3 to 9.7 nmol/kg in the deep or bottom waters. Aluminum values were higher than
in the surface waters of the central North Pacific, while minimum values were similar to levels in the intermediate or deep
waters of the central North Pacific, except for the bottom water over the slope. This suggests that the high Al concentration
in the surface reflects the large atmospheric input of Asian dust around the western side of the North Pacific region. On
the continental slope, Al concentrations in the upper 500 m depth decreased slopeward. This horizontal gradient of Al can
be explained from the combination of dilution by upwelling of Al-poor water originated from the North Pacific Intermediate
Water (NPIW) which intrudes into the mid-depth of the Okinawa Trough and the scavenging of Al by biogenic particles in the
continental slope zone. 相似文献
7.
Copper concentrations in surface waters off the southeastern United States coast range from 0.02 to 0.33 μg/kg (0.3–5.2 nmol/kg). Mean concentrations are lowest in Onslow Bay (0.07 μg/kg) and highest over the Blake Plateau (0.20 μg/kg). An explanation, compatible with the hydrography and hydrodynamics of the area, is proposed for the observed regional variations. 相似文献
8.
秋季东海二甲基亚砜的分布与影响因素研究 总被引：1，自引：0，他引：1
2010年11月对东海进行了大面调查,研究了秋季东海表层水中颗粒态和溶解态二甲基亚砜(DMSOp和DMSOd)的水平分布和PN断面的垂直分布特征及其影响因素。结果显示,表层海水中DMSOp和DMSOd的浓度范围分别为2.49~85.5nmol/L和2.27~86.6nmol/L,平均值分别为(17.2±1.40)nmol/L和(15.3±1.29)nmol/L。DMSOp水平分布与叶绿素a(Chl a)相类似,呈现近岸高、远海低的趋势,而DMSOd浓度高值区主要集中在东海西南部上升流区域。分析PN断面的垂直分布可见,DMSOp在近岸底层水中浓度较高,而DMSOd浓度在表层出现高值。相关性分析的结果表明,DMSOp与颗粒态二甲巯基丙酸内盐(DMSPp)以及DMSOp/Chl a比值与盐度分别存在一定的相关性,说明DMSOp与DMSPp具有相似的来源及生理功能。此外,DMSOd与二甲基硫(DMS)浓度具有正相关关系,说明DMS的氧化是东海DMSOd的一个重要来源途径。 相似文献
9.
10.
使用阴极溶出伏安法,利用2,3-二羟基苯丙氨酸(DHN)可以与Fe(Ⅲ)结合生成配合物,而BrO3-的加入可以催化该电化学反应的性质,系统研究了海水中溶解态Fe(Ⅲ)的最佳分析条件。结果表明,体系中添加20.0μmol/L DHN即可达到分析要求;添加BrO3-可以使溶出电流线性增大,选择的最终浓度为20.0mmol/L。当沉积电位为-0.20V,扫描速率为50.0mV/s,沉积时间为90s时,即可达到低铁海水的分析要求,在此条件下检测限为0.011nmol/L。紫外消解可以使测量灵敏度比未消解时提高13倍。用此方法测量得到的太平洋某处(158°15′E,22°23′N)海水表层水浓度为0.45nmol/L,75m处浓度为0.14nmol/L,1 500m处浓度为0.86nmol/L。 相似文献
11.
A method has been developed for the determination of ammonium concentration and isotopic enrichment in seawater samples at the low nanomolar range (10–100 nmol/kg). It is based on the reaction of phenol/hypochlorite with ammonium to form indophenol, with subsequent solid phase extraction, derivatisation and analysis by Gas Chromatography Mass Spectrometry. The precision of the method was maximised by incorporating a deuterated indophenol internal standard. A system was developed which generated seawater with extremely low ammonium concentrations thus matching sample and standard matrices for quantitative analysis. Data are presented from a study of ammonium regeneration rates at three stations in the oligotrophic North–East Atlantic where ambient ammonium concentrations were < 21 nmol/kg. Results suggested that ammonium availability for phytoplankton was limited by the rate of ammonium regeneration. Efficient ammonium assimilation contributed to the very low ambient ammonium concentrations measured at these stations. The study highlights the need for the accurate determination of ammonium regeneration rates in studies of new production, particularly in extreme oligotrophic conditions. If not corrected for isotope dilution, f-ratio estimates may be overestimated by 10.7–13.7%. 相似文献
12.
利用催化动力学分光光度法和两步提取法对2011年4月（春）、8月（夏）、10月（秋）和2012年1月（冬）桑沟湾海域溶解态无机锰(DIMn)和表层沉积物中的锰的含量进行测定。结果表明,桑沟湾4个季节（春季至冬季,后同）DIMn浓度呈现出近岸高、远岸低的分布特点,其平均浓度分别为(60.5±43.1) nmol/L、(42.0±30.5) nmol/L、(23.4±11.2) nmol/L和(18.2±13.5) nmol/L,呈现出明显的季节变化,即春季最高,夏季、秋季次之,冬季最低;与相邻的俚岛湾和爱莲湾相比,桑沟湾春季、夏季DIMn的浓度较高,秋季、冬季则没有显著性差异。桑沟湾表层沉积物中总Mn在4个季节的含量分别为(861±308) mg/kg、(915±322) mg/kg、(589±108) mg/kg、(653±185) mg/kg,表层沉积物中醋酸提取态Mn在4个季节的含量分别为(500±272) mg/kg、(502±232) mg/kg、(322±81) mg/kg、(345±91) mg/kg,两者均表现出近岸高、远岸低的分布特点。醋酸提取态Mn的含量在春季、夏季要显著高于秋季、冬季。悬浮颗粒物的吸附和浮游生物的利用是影响桑沟湾DIMn浓度与分布的重要因素。桑沟湾DIMn的源主要包括河流及地下水输送、大气输送、沉积物?水界面释放;汇主要包括养殖生物的清除、向黄海的输送等。简单箱式模型收支计算结果显示,桑沟湾DIMn的源略大于汇,表明除了养殖生物的清除和向黄海的输送,桑沟湾DIMn还存在其他汇。本研究的结果为桑沟湾DIMn的生物地球化学循环的深入认识提供了基础数据。 相似文献
13.
Bioassays were conducted with sea urchin and sand dollar sperm to determine the toxicity of chlorinated and unchlorinated sewage effluent and chlorinated and brominated seawater. The sperm cells were exposed to seawater dilutions of each toxicant for 5–15 min. The fertilisation of eggs served as the indicators of sperm viability. The effective concentrations which reduced fertilisation success by 50% (EC50) averaged 2·2 and 4·8% chlorinated and unchlorinated sewage in seawater, respectively. The sperm cells were extremely sensitive to chlorinated seawater at concentrations from 0·002 to 0·020 mg/litre total residual oxidant (TRO). Brominated seawater proved toxic to sperm in one test at 0·015 mg/litre TRO. Results of the sperm bioassays are compared with previous acute and chronic bioassays with fish. 相似文献
14.
《Deep Sea Research Part I: Oceanographic Research Papers》2003,50(10-11):1339-1352
Atmospheric iron and underway sea-surface dissolved (<0.2 μm) iron (DFe) concentrations were investigated along a north–south transect in the eastern Atlantic Ocean (27°N/16°W–19°S/5°E). Fe concentrations in aerosols and dry deposition fluxes of soluble Fe were at least two orders of magnitude higher in the Saharan dust plume than at the equator or at the extreme south of the transect. A weaker source of atmospheric Fe was also observed in the South Atlantic, possibly originating in southern Africa via the north-easterly outflow of the Angolan plume. Estimations of total atmospheric deposition fluxes (dry plus wet) of soluble Fe suggested that wet deposition dominated in the intertropical convergence zone, due to the very high amount of precipitation and to the fact that a substantial part of Fe was delivered in dissolved form. On the other hand, dry deposition dominated in the other regions of the transect (73–97%), where rainfall rates were much lower. Underway sea-surface DFe concentrations ranged 0.02–1.1 nM. Such low values (0.02 nM) are reported for the first time in the Atlantic Ocean and may be (co)-limiting for primary production. A significant correlation (Spearman's rho=0.862, p<0.01) was observed between mean DFe concentrations and total atmospheric deposition fluxes, confirming the importance of atmospheric deposition on the iron cycle in the Atlantic. Residence time of DFe in the surface waters relative to atmospheric inputs were estimated in the northern part of our study area (17±8 to 28±16 d). These values confirmed the rapid removal of Fe from the surface waters, possibly by colloidal aggregation. 相似文献
15.
《Marine Chemistry》2007,103(1-2):112-121
Several operationally defined fractions of phosphorus (P) were measured along a surface water transect in the North Pacific. The P content in all fractions was found to increase northward from the edge of the subtropical to the subarctic region. Particulate organic P (POP) concentrations increased from 9 to 110 nmol L− 1, whereas the particulate inorganic P (PIP) concentrations increased from 1 to 13 nmol L− 1. A significant correlation between POP, PIP and chlorophyll a suggested that these P pools are associated directly or indirectly with phytoplankton cells. PIP comprised 10–20% of the total particulate P pool across the transect, indicating it is an important component of the marine P cycle in this region. Dissolved non-reactive P (assumed to consist predominantly of non-reactive organic P compounds, thus referred to as DOP) concentration increased from 0.10 to 0.22 μmol L− 1, whereas soluble reactive P (SRP) concentration increased from 0.01 to 1.42 μmol L− 1 along the transect. The proportion of DOP and SRP varied widely, with a large proportion of DOP in areas with low total dissolved P concentrations in lower latitudes and a large proportion of SRP in areas with high total dissolved P concentrations in higher latitudes. High demand for DOP in the lower latitudinal region would diminish the concentration of this pool relative to higher latitudinal regions where SRP is more abundant and would be preferentially utilized. The availability of SRP could have a significant impact on the concentration and probably on the composition of DOP. We show that P fractionation provides an important insight for discussing the marine P cycle. 相似文献
16.
The concentration of dissolved and particulate Re have been measured in the Narmada, Tapi and the Mandovi estuaries in the Arabian Sea and the Hooghly estuary in the Bay of Bengal. Re concentration in water and particulate matter of these estuaries is highly variable. Re in river waters analysed varies from 1 to 41 pmol/kg, the lowest in the Mandovi and the highest in the Mahi river. Re concentrations in the rivers analysed except in the Mandovi river are higher than the average global riverine Re concentration of 2.1 pmol/kg. Based on this study and the available data, the contemporary global annual flux of dissolved riverine Re is estimated to be ~ 350 × 103 mol with an average concentration of ~ 9.2 pmol/kg, much higher than the earlier estimates. Residence time of Re in the oceans based on this estimate is 175,000 years, ~ 4 times lower compared to earlier estimates. Re behaves conservatively in all the estuaries studied. Re concentrations of seawater in the Bay of Bengal and in the Arabian Sea, estimated from the data of the Hooghly and the Mandovi estuaries respectively are ~ 40 pmol/kg, similar to the open ocean Re values of the Arabian Sea measured in this study and the values reported for in other oceanic regions. However, the dissolved Re in the Gulf of Cambay is 2 to 5 times higher, consistent with the high Re measured in the Mahi estuary and in the coastal waters of the Gulf of Cambay. The source of high Re in the Gulf of Cambay seems to be anthropogenic, measurements of Re in rivers and industrial waste waters draining into the Gulf supply amount to ~ 2300 mol of Re annually. This anthropogenic supply coupled with high residence time of water in the Gulf contribute to its high Re. Re concentration in suspended sediments of the Narmada estuary varies from 1 to 2 pmol/g, and does not show any discernible trend with salinity.The contemporary global riverine Re supply to the oceans estimated in this study is ~ 2–4 times higher compared to its removal in the reducing (anoxic/suboxic) sediments, indicating non-steady state of Re in the ocean. High dissolved riverine Re flux coupled with high Re content in the Gulf of Cambay highlights the need of a detailed study of Re in the various global rivers and in oceans including coastal regions and semi enclosed basins of the world to understand its behaviour in various reservoirs and to constrain the residence time of Re in the ocean. 相似文献
17.
《Marine Chemistry》1987,21(3):203-211
Seawater samples and airborne particulate material were collected in the subtropical North Atlantic during R.V. “Meteor” Cruise M60 (N34°47.2′W26°57.7′/N10°1.3′W32°58.3′). Hydrocarbon concentrations were estimated in the samples. For seawater the concentrations ranged from 0.2 μg to 3.5 μg dm−3. In the open ocean air the concentrations of the particulate hydrocarbon measured at 14m above sea level ranged from 2.8 ng to 133.1 ng m−3. A significant increase was observed during a Saharan dust outbreak. Comparison with aluminium concentrations in seawater and in the air suggests input of atmospheric hydrocarbons by dry deposition to be an important transportation pathway. 相似文献
18.
P. Bienfang E.H. De Carlo S. Christopher S. DeFelice P. Moeller 《Marine Chemistry》2009,113(3-4):164-171
The objective of this work is to characterize the concentrations of selected trace elements (V, Mn, Ni, Fe, Co, Cu, Zn, Se, As, Mo, Cd, Pb, U) in diverse nearshore (50 m), coastal (1.5 km) and seawater well environments within the Hawaiian Archipelago using robust analytical methods that are appropriate for metals analyses in seawater. The sampling sites include locations having varying type, quality and quantity of freshwater input. In most coastal and nearshore cases, the trace element concentrations approximate values characteristic of offshore waters. Concentrations of trace elements in coastal waters that were enriched through either urban or agricultural inputs declined sharply within a short distance from shore; this is taken to indicate the predominant importance of physical mixing/advective processes along with particle scavenging in these dynamic areas. Trace element levels in seawater wells did not evidence any concentration trends consistent with island age suggesting little or no impact of island weathering on metal concentrations; concentration differences among wells appeared to be more dependent on well depth, redox conditions, and/or salinity. Sampling also targeted nearshore locales where ciguatera fish poisoning is prominent because of suggested linkages between trace element concentrations and aberrant dinoflagellate growth. Nearshore stations where ciguatera is prevalent failed to show clearly different trace element levels except for two prominent locales which showed elevated Mn and Fe concentrations. 相似文献
19.
Shizuko Hirata 《Marine Chemistry》1985,16(1):23-46
Phosphorus and metals bound to organic matter were separated from coastal sediments of Harima Sound in Seto Inland Sea, Japan by extraction with NaOH and fractionated by Sephadex G-25 chromatography. Phosphorus and metals were determined in the eluates by a multi-channel, inductively coupled plasma-atomic emission spectrometer. Phosphorus and Cu, Zn, Fe, Mn, Ni, Cr, Co and Ti bound to organic matter with high molecular weights (OMHMW) (MW ? 5000) were found to be present in the sediments, but no Mo or V were found. The technique provides minimum estimates of the amounts of P and metals bound to organic matter. These organic complexes show surface enrichment in a sediment core (0–20 cm) and their contents decrease with depth. Also, the amounts of eighteen elements, namely: P, Fe, Mn, Zn, Cu, Si, Al, Ti, Pb, Co, Ni, Cr, Mo, V, Na, K, Ca and Mg, in H2O, ammonium acetate at pH 7 and 5, hydrogen peroxide, hydroxylamine hydrochloride and hydrogen fluoric acid soluble fractions have been determined with a selective chemical leaching technique for the 210Pb-dated sediment core sample. Considerable amounts of P (6–19%) and Cu (5–21%) were associated with organic matter, in contrast to other metals such as Fe, Mn, Zn, Ni, Cr, Co and Ti which were associated with sulfide and silicate. 相似文献
20.
A new method for the quantification of different redox-species of molybdenum (V and VI) in seawater 总被引：1，自引：0，他引：1
A new method for the direct determination of reduced and oxidized Mo species (Mo (V) and Mo (VI)) in seawater was developed and used for the first time. The method includes the complexation of Mo (V) with tartrate, solid phase extraction of the Mo (V)–tartrate complex by a XAD 7HP resin, followed by elution with acidic acetone. In this study, the eluted Mo (V) was quantified by graphite furnace atomic absorption spectrometry. The detection limit of this protocol was on the order of 0.2 nM. The analytical precision was 10% of ~ 10 nM. This method was successfully applied to the determination of Mo (V) and Mo (VI) in surface and bottom waters at the head of Peconic River Estuary. Total Mo (Mo (V) + Mo (VI)) ranged from 100–120 nM in most bottom saline waters, and 2.5–15 nM for surface fresher waters. Concentrations of Mo (V) in these environments ranged from 0 nM to ~ 15 nM, accounting for 0%–15% of the total dissolved Mo pool. The time series experiments showed that the Mo speciation changed within 1 h after the water collection, and therefore it is strongly suggested that speciation analysis be carried out within the first 15 min. However, since these are the first Mo speciation data in concentration ranges typical of normal marine and coastal waters, additional research may be required to optimize the methodology and further explore Mo cycling mechanisms. 相似文献