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1.
A study on the curves of the exchange ratio E(%)-pH on the liquid-solid interface of the systems Zn(II) with clay minerals (Kaolinite , illite and montmorillonite), Zn(II) with hydrous ferric oxides (amorphous ferric oxide, goethite and hematite). Zn(II) with hydrous manganese oxide (y-MnOOH, manganite and 5-MnO2) etc . in seawater resulted in the discovery of new plateau type exchange ratio ?%)-pH curves not yet reported in literature. The two factors that decide the growth , decline and the change of the " plateau type " curve are : (1) the inherent characteristics of systems , which can be explained by the exchange constants i(i=1 ,2 , 3 . etc .) of interfacial stepwise ion / coordination particle exchange between liquid and solid ; and (2)The theory of interfacial stepwise ion/coordination(the amount of solid exchange reagent)particle exchange in seawater was applied to explain the experimental results of the above study and a general formula was derived for the plateau type exchange ratio E(%)-pH c  相似文献   

2.
A study on the curves of the exchange ratioE(%)- pH on the liquid-solid interface of the systems Zn (II) with clay minerals, (Kaolinite, illite and montmorillonite), Zn (II) with hydrous ferric oxides (amorphous ferric oxide, geothite and hematite), Zn (II) with hydrous manganese oxide (γ-MnOOH, manganite and δ-MnO2) etc. in seawater resulted in the discovery of new plateau type exchange ratioE(%)-pH curves not yet reported in literature. The two factors that decide the growth, decline and the change of the “plateau type” curve are: (1) the inherent characteristics of systems, which can be explained by the exchange constants (i=1, 2, 3, etc.) of interfacial stepwise ion/coordination particle exchange between liquid and solid; and (2) . The theory of interfacial stepwise ion/coordination particle exchange in seawater was applied to explain the experimental results of the above study and a general formula was derived for the plateau type exchange ratioE(%)-pH curves. The theoretically simulated and calculated curves coincided well with the experimental results. This paper provides new and powerful experimental basis to support the theory of interfacial stepwise ion/coordination particle exchange in seawater. The project was supported by the National Natural Science Foundation of China.  相似文献   

3.
Benthic nutrient recycling in shallow coastal waters of the Bohai Sea   总被引：3，自引：0，他引：3  
Sediment-water fluxes of N and P species in the Bohai Sea were investigated in September-October 1998 and April-May 1999. The benthic fluxes of nutrient species were determined by incubating sediment core samples with bottom seawater bubbled with air or nitrogen. NO^-2,NH4, dissolved organic nitrogen (DON) and phosphorus (DOP), total dissolved nitrogen (TDN) and phosphorus (TDP), and PO4^3- showed a net exchange flux from seawater to sediment, while NO^-3, dissolved inorganic nitrogen (DIN) and SiO3^2- were released from sediment to seawater in the Bohai Sea. Sediment-water nutrient exchange increases DIN and reduces the phosphorus load in the Bohai Sea. The release of silicate from sediment to overlying seawater reduces potential silicate limitation of primary production resulted from decrease of riverine discharge.The exchange flux of nutrients showed no obvious seasonal variation. The present study showed that the concentrations and composition of nutrients in the water column were affected by suspended sediment, and that not all the exchangeable phosphate in sediment could be released via sediment resuspension.  相似文献   

4.
In seawater, aside from metal elements and suspended particles, organic substances amount to about 500–2,000 ug carbon/l[8], which is not neglegible in comparison with that of minor metal elements. But in the study of the interaction of the three constituents (metal elements, organics, and suspended particles), the effect of organics in seawater on the surface reaction of metal element—suspended particles has usually been neglected. Recent theoretical research[1, 11] confirmed the importance of the effect of organics in seawater on the surface reaction of metal element—suspended particles. Generally, the effect of organics on the reaction of metal ions, especially Cu(II), on a solid surface is either promotive[2] or inhibitive[7, 9]. So far the fact that organics cannot affect the surface reaction of Cu(II) ions on solids has not been reported in literature. Our experimental results showed that none of the amino acids in seawater affect Cu(II)-goethite ion exchange under certain experimental condition (such as amino acid of lower concentration and lower pH). It was known that the metal ion-organics complex in a liquid competing with solids for metal ions may inhibit the surface reaction of metal ions on solids, but the mechanism of the complex reaction of metal ions competing with solids is not known yet. In fact, the decrease of surface site-exchanging due to the surface reaction of organics on solids is also inhibitive. It is also explained by the ion exchange isotherm of the “amino acid-Cu(II)-geothite” system. This result further demonstrates that the theory of interfacial stepwise ion exchange is applicable to the metal ion exchange isotherm with the presence of organic substances in the system. Projects supported by the Science Fund of the Chinese Academy of Sciences  相似文献   

5.
1Introduction GamakBay,anegg shapedseasurfaceareaofap proximately112km2,isasemi enclosedshallowwaterareawithameandepthof9mandhasbotheastandsouthchannelstoreceiveseawaterfromoutside(seeFig.1).Similarscalesoftidalwavesalmostsimultane ouslyenterorexitthrough…  相似文献   

6.
ＩＮＴＲＯＤＵＣＴＩＯＮＴｈｅｖａｒｉｏｕｓｐｈｙｓｉｃａｌａｎｄｃｈｅｍｉｃａｌｒｅａｃｔｉｏｎｓｔｈａｔｏｃｃｕｒｂｅｔｗｅｅｎｔｈｅｓｕｓｐｅｎｄｅｄｐａｒｔｉｃｌｅｓ,ｓｅｄｉｍｅｎｔｓ,ｅｔｃ.ａｎｄｈｅａｖｙｍｅｔａｌｓｉｎａｎａｔｕｒａｌａｑｕａｔｉｃｓｙｓｔｅｍｐｌａｙｅｘｔｒｅｍｅｌｙｉｍｐｏｒｔａｎｔｐａｒｔｓｉｎｃｏｎｔｒｏｌｌｉｎｇｔｈｅｄｉｓｔｒｉｂｕｔｉｏｎｐａｔｔｅｒｎ,ｍｉｇｒａｔｉｏｎａｎｄｔｒａｎｓｆｏｒｍａｔｉｏｎｏｆｈｅａｖｙｍｅｔａｌｓｔｈｅｒｅ.Ｓｉｎｃｅ…  相似文献   

7.
The ocean is an important inventory of anthropogenic mercury(Hg),yet the history of anthropogenic Hg accumulation in the ocean remains largely unexplored.Deep-sea corals are an emerging archive of past ocean chemistry,which take in sinking or suspended particulate organic matter as their food sources.Such organic matter would exchange Hg with the local seawater before being consumed by the deepsea corals.As such,the organics preserved in the coral skeleton may record the Hg evolution of the ambient seawater during the time of coral growth.Here,we report the first data on Hg concentrations variability of a deep-sea proteinaceous coral in the oligotrophic North Pacific at the water depth of 1 249 m,in attempt to understand the transfer of anthropogenic Hg into the deep Pacific ocean over the last seven centuries.We find that the Hg concentrations of different coral growth layers have remained relatively constant albeit with considerable short-term variability through time.The overall stable Hg concentration of the last seven centuries recorded in our sample suggests that anthropogenic pollution is not yet a clearly resolvable component in the deep oligotrophic North Pacific waters,in agreement with rece nt estimation from modelling works and observational studies of modern seawater profiles.As there is hardly an unambiguous way to separate anthropogenic Hg from the natural background based on recent seawater profiles,our historical data provide valuable information helping to understand the oceanic cycle of Hg through time.  相似文献   

8.
The isotherms of the interaction between the suspended particles and Cu2+, and the effects of lysine and asparaginic acid on the isotherms in the Huanghe (Yellow) River were studied by applying the theory and method of interfacial stepwise ion/coordination particle exchange. We obtained a new stepped river isotherm, formed by two curves joined together with a “plateau” in the middle. The adsorption equilibrium constantsK 1 andK 2 were calculated by using the isothermal equation of surface stepwise ion exchange. Amino acid in small amount promotes exchange adsorption of the suspended particles with Cu2+. The degree of promotive action relates to the isoelectric point of amino acid. The promotive effect of lysine is bigger than that of asparaginic acid. Project 29361001 supported by NSFC.  相似文献   

9.
1Preface Todescribeoceanicintermediatewatermasses,itis necessarytohaveawell definedstudyframeorsurfacebecauseofthefluctuationnatureofintermediatewa ters.Itiswellunderstoodthatoceanicwater mass mixingdoesnotalignwitheitheraconstantgeopoten tialdepthorapropertysurfacesuchastemperature,salinity,pressureanddensitysurfacesbutfollowsa neutraldensitysurface.Thisisbecauseawaterparcelmovesasmalldistanceisentropicallyandadiabaticallyontheneutraldensitysurfacewithoutdoingworka gainstabuoyantrestoringforc…  相似文献   

10.
This article deals with a new type of isotherm discovered in sea water systems. The characteristics of this type of isotherm are the non-linear exponential relationship in the low concentration region and the isotherm composed of two or three “S” curves with one or two plateaus in the middle. This isotherm cannot be expressed by the isotherm equation used in marine chemistry at present.[7] Besides, there has been no report in literature about this type of isotherm in so far as the reaction of minor elements on hydrous oxides is concerned. In order to explain theoretically this type of isotherm, this article suggests the use of the theory of interfacial stepwise ion/coordination particle exchange (for simplicity, ion exchange is used herein-after) of suspended particles to deduce a corresponding isotherm equation. Proceeding from the isotherm of this article, we made theoretical analyses of these two characteristics as well as experiments in verification thereof. Twenty-four systems of experiments on this new type of isotherm and isotherm equation were designed and conducted. Experiment results agree with the theory reported here. Project supported by the Science Fund of the Chinese Academy of Sciences.  相似文献   

11.
This review article commences with a comprehensive historical review of the evolution and application of various density surfaces in atmospheric and oceanic studies. The background provides a basis for the birth of the neutral density idea. Attention is paid to the development of the neutral density surface concept from the nonlinearity of the equation of state of seawater. The definition and properties of neutral density surface are described in detail as developed from the equations of state of seawater and the buoyancy frequency when the squared buoyancy frequency N2 is zero, a neutral state of stability. In order to apply the neutral density surface to intermediate water-mass analysis, this review also describes in detail its practical oceanographic application. The mapping technique is focused for the first time on applying regularly gridded data in this review. It is reviewed how a backbone and ribs framework was designed to flesh out from a reference cast and first mapped the global neutral surfaces in the world＇s oceans. Several mapped neutral density surfaces are presented as examples for each world ocean. The water-mass property is analyzed in each ocean at mid-depth. The characteristics of neutral density surfaces are compared with those of potential density surfaces.  相似文献   

12.
IR spectra of Cu (II)-marine solid particle systems show that Cu(II)-marine solid particle ion exchange causes a stepwise change in the surface H-bonding hydroxyl groups on illite, montmorillonite, CaCO3, γ-AlOOH and goethite, but that this does not affect the surface free hydroxyl groups on illite, montmorillonite and CaCO3, and framework hydroxyl group on goethite and on γ-AlOOH. Over the range of Cu (II) exchange amounts in the present experiment, four stepwise changes were discovered for the surface H-bonding hydroxyl group on illite, while two stepwise changes were observed on the other marine solids. The interfacial stepwise ion exchange theory was first demonstrated by the above experimental evidence.  相似文献   

13.
MODUonONThermsurmtofdissolvedorganiccarbon.(DoC)inseawaterhasprovedtobeaddricultandcontroversialproedurepeenneretal.,l992,l993,OgawaandOgam,l992,Tanoue,l992).InterestinthemeasurernentofDOCinseaytteyintenSfomtlyinoonnographicdedes(Sharp,l993)largeyduetothesuggestionthathighteIneratU-rcatalyticoxidationanalysisyieklshighervaluesthanhaditionalweoxidationmethods(SugdriraandSuzuki,l988).Thereportedhigherconcenttationsappeatalsignilicantforg1obaloasnfluxmodelingcyoggweiler,l992)andforunderst…  相似文献   

14.
The anodic stripping voltammetry with physically-coating mercury film electrode was used to investigate the complexing action of trace heavy metals in seawater with organic ligands. The apparent copper complexing capacity of seawater was determined by titrating the organic ligands in natural seawater with standard ionic copper solution. The complexing actions of copper in seawater with humic acid (HA) or fulvic acid (FA) were investigated by titrating copper in seawater with HA or FA solution. The equilibrium time, electrodeposition potential, and effect of pH etc. were investigated respectively. The results show that the interaction of copper in seawater with organic matter is a fast process. At natural pH, HA or FA tend to act with copper in seawater to form nonlabile complexes. During experimental electrode process, these complexes did not significantly dissociate. The experimental results were calculated according to 1∶1 complex formation.  相似文献   

15.
This article deals with the interaction of zinc with δ−MnO2, γ−MnOOH and manganite existing in natural water systems. The mechanism of the reaction has been studied in detail. From the fact that the “ratio of ion exchange(%)-pH” graph is an “S shaped” curve, it is possible to deduce that the chemical reaction is of the nature of cation exchange. And since the pH range of ion exchange=4, it is possible to further deduce that the reaction can be explained by the mechanism of monovalence cation exchange. The main result of this article is the discovery of a new type of isotherm which has not been mentioned in previous literature here and abroad. This isotherm cannot be represented by any presently available adsorption isotherm equations in marine chemistry. The characteristics of this new type of isotherm are as follows: the isotherm has two “knees” and three “plateaus”, the heights of these three “plateaus” are in the ratio 1:2:3. In order to explain theoretically our new isotherm, this article suggests the application of the principle of interfacial stepwise ion exchange for liquid-solid distribution of minor elements on suspended particulate matter. The corresponding isotherm equation was derived from this theory. The results obtained in this article will be of theoretical guiding significance in the study of the marine geochemistry of zinc. Projects supported by the Science Fund of the Chinese Academy of Sciences.  相似文献   

16.
In this study, seawater was pumped up from 150, 200, 300, 500 and 1000 m in the South China Sea and analyzed to make certain what depth should deep-sea water (DSW) be pumped up for medicinal usage. The pumping depth of DSW was determined on the basis of chemical ingredients. The analyses of inorganic elements and dissolved organic matter (DOM) were performed by inductively coupled plasma mass spectrometry (ICP-MS) and ultra performance liquid chromatography-mass spectrometry (UPLC-MS) respectively. The raw data were used for hierarchical cluster analysis (HCA) and principal component analysis (PCA). The results showed that seawater pumped up from 500 m and 1000 m was similar in their chemical ingredients, and was different from the seawater pumped up from other depths. These results indicated that seawater from more than 500 m depth had relatively stable chemical ingredients and could be used as DSW in the South China Sea.  相似文献   

17.
A neutral density surface is a logical study frame for water-mass mixing since water parcels spread along such a surface without doing work against buoyancy restoring force. Mesoscale eddies are believed to stir and subsequently mix predominantly along such surfaces. Because of the nonlinear nature of the equation of state of seawater, the process of accurately mapping a neutral density surface necessarily involves lateral computation from one conductivity, temperature and depth （CTD） cast to the next in a logical sequence. By contrast, the depth of a potential density surface on any CTD cast is found solely from the data on this cast. The lateral calculation procedure causes a significant inconvenience. In a previous paper by present author published in this journal （You, 2006）, the mapping of neutral density surfaces with regularly gridded data such as Levitus data has been introduced. In this note, I present a new method to find the depth of a neutral density surface from a cast without having to specify an integration path in space. An appropriate reference point is required that is on the neutral density surface and thereafter the neutral density surface can be determined by using the CTD casts in any order. This method is only approximate and the likely errors can be estimated by plotting a scatter diagram of all the pressures and potential temperatures on the neutral density surfaces. The method assumes that the variations of potential temperature and pressure （with respect to the values at the reference point） on the neutral density surface are proportional It is important to select the most appropriate reference point in order to approximately satisfy this assumption, and in practice this is found by inspecting the θ-p plot of data on the surface. This may require that the algorithm be used twice. When the straight lines on the θ-p plot, drawn from the reference point to other points on the neutral density surface, enclose an area that is external to the cluster of θ-p points of the neutral density surface, errors will occur, and these errors can be quantified from this diagram. Examples showing the use of the method are presented for each of the world＇s main oceans.  相似文献   

18.
Coastal lagoons with small catchment basins are highly sensitive to natural processes and anthropogenic activities. To figure out the environmental changes of a coastal lagoon and its contribution to carbon burial, two sediment cores were collected in Xincun Lagoon, southeastern Hainan Island and (210) ~Pb activities, grain size parameters, total organic carbon(TOC), total nitrogen(TN), total inorganic carbon(TIC) and stable carbon isotopes(δ~(13)C) were measured. The results show that in 1770–1815, the decreasing water exchange capacity with outer open water, probably caused by the shifting and narrowing of the tidal inlet, not only diminished the currents and fined the sediments in the lagoon, but also reduced the organic matter of marine sources. From 1815 to 1950, the sedimentary environment of Xincun Lagoon was frequently influenced by storm events. These extreme events resulted in the high fluctuation of sediment grain size and sorting, as well as the great variation in contributions of terrestrial(higher plants, soils) and marine sources(phytoplankton, algae, seagrass). The extremely high content of TIC, compared to TOC before 1950 could be attributed to the large-scale coverage of coral reefs. However, with the boost of seawater aquaculture activities after 1970, the health growth of coral species was severely threatened, and corresponding production and inorganic carbon burial flux reduced. The apparent enhanced inorganic carbon burial rate after 1990 might result from the concomitant carbonate debris produced by seawater aquaculture. This result is important for local government long-term coastal management and environmental planning.  相似文献   

19.
掌握澳门附近海域沉积物的污染状况及特征,对于合理安排澳门海洋海岸工程疏浚泥的海洋倾倒,防止造成海洋污染有十分重要的意义。根据1997—1999年连续三年对澳门附近主要区域的海洋沉积物采样测定结果,通过分析认为澳门附近海域沉积物污染具有下列特征:1)沉积物中重金属和油类含量普遍较高,除了总Hg外均高于珠江口海区的其他港口;2)沉积物中污染物的分布受人类活动的影响明显,澳门内港受船只排污、码头作业、陆地工业和生活污水排放的影响,是澳门附近海域沉积物污染最为严重区域;3)受水质交换的影响明显,澳门外港、路环岛东北等区域受珠江径流影响水质交换较快,沉积物中污染物的含量较低,而内港由于水质交换较差,沉积物中污染物的含量相对较高;4)与沉积物的成分组成(吸附)有关,大部分污染物与沉积物中粉砂有较好的相关性,表明粉砂对污染物质有较广泛性的吸附能力,尤其是Cu、Zn、Cd、油类、有机质。  相似文献   

20.
The removal processes of major seawater chemical constituents in the Bohai Sea include seawater ex-change between the Bohai Sea and the Northern Yellow Sea,cation exchange,interstitial water burialand spray,formation of illite,sepiolite,sulfate and sulfur,and carbonates.The mass balance calculationbased on these processes is very applicable to the Bohai Sea.  相似文献   

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