全球百年海表面温度年际和年代际变化特征分析

利用100 a(1903—2002年)HadiSST的逐月资料,将全球海表面温度异常(SSTA)作为整体进行经验正交函数分解(EOF分解),提取了控制各大洋SSTA的主导模态和各大洋之间的联合模态,分析了相应的空间分布和时间序列。研究结果表明:SSTA变化最剧烈的海区是赤道中东太平洋、西北大西洋湾流海区和北太平洋黑潮延伸体海区。热带太平洋厄尔尼诺和南方涛动是主导模态并具有2~7 a周期的年际变化;SSTA变化第二主模态和第三主模态都是以大约70 a为周期的年代际变化为主的跨大洋联合模态。第二主模态的空间分布主要表现为中纬度北太平洋和北大西洋反位相、热带太平洋与大西洋反位相的太平洋-大西洋双偶极子型分布。SSTA变化的第三模态主要呈现南北半球海洋反位相的特征,为北太平洋-北大西洋-南大洋联合模态。第四模态基本上是反映各个不同海域特有的局地海洋-大气相互作用模态,该模态的时间序列具有1~4 a周期的年际变化和约9 a周期的年代际变化。     

A global analysis of multi-mode sea surface temperature pattern

1 IntroductionThe variability of the air -sea system orches-trates a complex climate system of our earth, andthis variability gives rise to an array of naturally oc-curring dynamical modes at different time scales.These modes are important attributes of c…     

Distribution and Seasonal Variability of Organic Matter in a Small Eutrophicated Salt Lake

Distribution and seasonal variability of dissolved organic carbon (DOC) and surface active substances (SAS) were studied along the depth profile (15 m) in a small eutrophicated and periodically anoxic sea lake (Rogoznica Lake, Eastern Adriatic coast) in 1996 and 1997. The range of DOC concentrations was characteristic for productive coastal marine ecosystems (60% of samples in the range of 1–2 mg l⁻¹and 40% between 2 and 3 mg l⁻¹). Distribution of SAS concentrations was uniform and shifted toward higher concentrations in comparison to other coastal areas in the Adriatic Sea. Eutrophication in the lake is generated by nutrient recycling under anaerobic conditions. Systematically higher concentrations of chlorophyll a, DOC and SAS were determined at the chemocline in the bottom layer (10–12 m) than in the upper water layer (0·5–2 m). Seasonal variability of organic matter was discussed regarding distributions of microphytoplankton (cells >20 μm) and photosynthetic pigments as well as oxygen and salinity changes along the depth profile. The dissolved oxygen saturation reaching up to 300% in the water layer between 8 m and 10 m depths in May and June 1996, was correlated with enhanced concentrations of phytoplankton biomass (reflected as chl a and b, fucoxanthin, peridinin, zeaxanthin) and increased concentrations of DOC and SAS.     

Direct determination of surface active substances in natural waters

Advantages of direct determination of surface active substances without sample pretreatment, using the electrochemical method (a.c. polarography) based on the measurement of adsorption effects on the mercury electrode, are illustrated for a number of freshwater and marine samples and phytoplankton culture media. The effects of dilution, filtration and centrifugation of samples were investigated. A high loss of organic material through filtration was observed for selected sea surface microlayer samples and phytoplankton culture media. The samples were compared with different model surfactants and were found to possess similar adsorption characteristics to hydrophobic, fatty surfactants. The freshwater samples were found to be more stable during pretreatment than the marine samples. Humic substances are the predominant surface-active compounds in freshwater systems. The use of a calibration curve for humic material is proposed for the rapid and direct determination of surfactant activity values for freshwater samples.     

Possibilities of using optical spectral analysis to estimate characteristics of roughness in the presence of films on the sea surface

The possibility of using an optical spectrum analyzer (OSA) to determine the degree of short gravity-capillary wave damping by films of surface-active substances (SAS) is studied. Nonlinear mechanisms of optical surface imaging associated with a complex profile of sky brightness and long waves are analyzed. Using the model of free short gravity waves damping by the films, it is shown that the difference between the contrast of roughness and imaging in film-covered surface regions can be substantial and attributed to a variability of the damping degree within a specified wavelength range rather than to the wave-damping value. In addition, it is illustrated that Doppler shifts of the OSA space-time spectrum in regions covered with films can substantially increase due to nonlinear distortions of the surface images. This fact should be taken into account when obtaining additional information on the state of the surface and roughness based on the Doppler shift values.     

Determination of surfactant activity and anionic detergents in seawater and sea surface microlayer in the Mediterranean

The study of the physico-chemical properties and the determination of different classes of organic substances in the sea are of substantial interest and importance for understanding biogeochemical processes in the sea. The preferable method should be sensitive enough for direct measurement without pretreatment procedures in order to avoid changes in the composition of organic substances initially present in the sample.Surfactant activity data are presented here as measured by electrochemical methods during 1979, 1980 and 1981 in samples from open waters of the Western Mediterranean, and in a few characteristic coastal areas of the Adriatic Sea with different biological activity and different influence of man's activities. Data on sea surface microlayer samples collected during 1977, 1978 and 1981 at different locations and seasons in the Rijeka Bay, which is an integral part of the Adriatic Sea, are presented and discussed in more detail.It was found that the type and concentration of natural surface active material vary within different Mediterranean regions and along the depth profile of the water column.Petroleum hydrocarbons and detergents were found to be prevalent pollutants responsible for high surfactant activity values. Pollution effects are most pronounced in the sea surface microlayer.Electrochemical methods are proposed for research and monitoring of surface-active substances in the sea.     

Estuarine transformation of organic matter: single coalescence events of estuarine surface active particles

Individual surface-active particles (SAP) in aqueous environmental samples can be characterized through their coalescence at a model hydrophobic interface. Each coalescence event is recorded as an electrical signal. As the electrical signal is a current transient (time on a millisecond scale), the sequence of fast processes leading to the formation of a condensed film can be studied from the moment of first attachment at the interface.In the stratified Krka Estuary, SAP are present in maximum concentrations (10⁷−5 × 10⁸ particles l⁻¹ min the size range > 1 μm) at the halocline (freshwater-seawater interface). This highly surface-active fraction of particulate organic matter can be viewed as oily droplets. SAP are fluid, and are readily transformed at interfaces to films of molecular thickness (surface area per particle is in the range 10⁻⁵–10⁻² cm²).Comparison of response of individual SAP with model particles, and the frequency of their appearance in estuarine samples, shows that a majority of estuarine SAP has, in terms of viscosity and film permeability, the properties of oleic acid. A significant fraction of SAP have more rigid structures, comparable to moleic acid + cholesterol model particles. A small fraction ( > 1%) behaves as phytoplankton cells with fluid outer membranes.We have also presented evidence for a strong interaction between elemental mercury and SAP, which is not sensitive to the molecular structure of the organic phase. The puzzling accumulation of mercury at the halocline of the Krka Estuary may be regarded as the result of interaction of elemental mercury with SAP.     

Factors influencing the daily behaviour of dissolved gaseous mercury concentration in the Mediterranean Sea

Mercury evasional fluxes from the sea surface into the atmosphere play an important role in the Hg biogeochemical cycle, especially in the Mediterranean basin, which is characterized by the presence of large cinnabar deposits, intense solar radiation and high temperatures for many months of the year. Since the available experimental methodologies to measure mercury flux can be used only in good weather conditions, at present it is necessary to make use of exchange models that require the knowledge of the dissolved gaseous mercury (DGM) concentration in seawater. In this paper, the main factors affecting DGM levels are discussed considering the determination of the DGM daily behaviour in different meteo-marine and weather conditions at coastal and offshore locations of the Mediterranean basin. A fully automatic device for continuous analyses of DGM concentration with a high time resolution was used. Results show that the daily trend of DGM concentration tracks that of the solar radiation intensity, often mapping the movement of the clouds. DGM levels can be decreased by the presence of high winds that increase mercury evasion from the water surface, as well as by the mixing of the surface water layer. The presence of high levels of dissolved organic matter favours the photo-induced reduction of mercury as observed by the measurements performed in a lagoon water.     

Concentrations of cadmium,copper, lead and zinc in surface waters of the Northwest Atlantic Ocean — A comparison of Go-flo and teflon water samplers

The concentrations of cadmium, copper, lead and zinc were measured at two locations in surface waters of the western North Atlantic. Samples were collected upstream of the research vessel in 1-1 teflon bottles, and in a 30-1 teflon-coated Go-flo bottle. Surface mixed-layer samples were also collected at each location by ship cast using this same Go-flo sampler. A comparison of the three sampling modes shows that all the samples taken with the Go-flo sampler possessed much higher concentrations of zinc (7–10-fold) and lead (2–3-fold) than those collected directly in teflon bottles. No apparent differences were noted at each station in the concentrations of either copper or cadmium among the samples collected by the three different procedures. The measured values for copper and cadmium in these waters are in good agreement with recent reports for the western North Atlantic.     

Analysis of seawater for dissolved cadmium, copper and lead: An intercomparison of voltammetric and atomic absorption methods

An intercomparison study of voltammetric and atomic absorption spectrometric methods for determining cadmium, lead and copper in seawater samples was conducted. The voltammetric approach utilizes differential pulse anodic stripping voltammetry using a rotating, glassy carbon, mercury film electrode under conditions developed to minimize contamination sources and to enhance sensitivity for seawater matrices. The atomic absorption approach involves a concentration step using either an organic solvent extraction of metal dithiocarbamate chelates or a Chelex-100 column with detection by graphite furnace atomic absorption spectrometry. Similar and consistent results were obtained using both methods for the three trace metals studied on a wide range of natural seawater samples. Both methods are comparable in sensitivity for cadmium and copper, however the voltammetric method is better suited for the analysis of lead in seawater because of its enhanced sensitivity and low blank. An advantage of the voltammetric approach is its amenability towards real-time shipboard analysis.     

Complexation of mercury by dissolved organic matter in surface waters of Galveston Bay, Texas

The chemical speciation of dissolved mercury in surface waters of Galveston Bay was determined using the concentrations of mercury-complexing ligands and conditional stability constants of mercury-ligand complexes. Two classes of natural ligands associated with dissolved organic matter were determined by a competitive ligand exchange-solvent solvent extraction (CLE-SSE) method: a strong class (L_s), ranging from 19 to 93 pM with an average conditional stability constant (K_HgLs) of 10²⁸, and a weak class (L_w) ranging from 1.4 to 9.8 nM with an average K_HgLs of 10²³. The range of conditional stability constants between mercury and natural ligands suggested that sulfides and thiolates are important binding sites for dissolved mercury in estuarine waters. A positive correlation between the estuarine distribution of dissolved glutathione and that of mercury-complexing ligands supported this suggestion. Thermodynamic equilibrium modeling using stability constants for HgL, HgCl_x, Hg(OH)_x, and HgCl(OH) and concentrations of each ligand demonstrated that almost all of the dissolved mercury (> 99%) in Galveston Bay was complexed by natural ligands associated with dissolved organic matter. The importance of low concentrations of high-affinity ligands that may originate in the biological system (i.e., glutathione and phytochelatin) suggests that the greater portion of bulk dissolved organic matter may not be important for mercury complexation in estuarine surface waters.     

Organic matter characterization and fate in the sub-arctic Norwegian fjords during the late spring/summer period

The organic matter (OM) pool has been studied in two sub-arctic north Norwegian fjords, Balsfjord and Ullsfjord, in July 2001 and June 2003. Besides general OM parameters such as dissolved organic carbon (DOC), particulate organic carbon and nitrogen (POC and PON), the distribution of specific compounds such as folic acid and surface active substances (SAS) was followed. The results are supported with data of salinity, temperature, and chlorophyll a (Chl a). This approach allowed assessment of the fate of the OM pool, and its distinct vertical, spatial, and seasonal variations. Fjord waters could be vertically divided into two layers: the upper mixed layer (UML), until 40 m depth, and the deep aphotic layer. Spatial variability between the two fjords is a consequence of different influences of shelf waters on the fjords. Significant enrichment of POC and PON concentrations (3–5 times), as well as those of particulate SAS and folic acid (up to 3.2 times) in the UML was recorded during the period of new production, in early June. Depletion of particulate OM in deep waters was ascribed to fast dissolution or remineralization in the UML or upper part of aphotic layer. OM in July 2001 was characterized with 15.9% higher DOC pool compared to June 2003, and had refractory properties, suggesting the fjords to be an important source of organic matter for the continental shelf ecosystem. The DOC pool in these subarctic fjords represents the major component of the OM pool. The DOC concentrations in fjords are lower than those in previously studied warmer seas (e.g. the Adriatic Sea), whereas the concentrations of folic acid and SAS are comparable to those in the Adriatic Sea.     

Distribution of surface-active substances in the northern Adriatic Sea

Spatial distribution and seasonal variability of surfactant activity (SA) of seawater were studied in the northern Adriatic Sea and compared to the temperature and salinity patterns in the 2-year period from February 1998 to January 2000, based on monthly surveys. Surface-active substances (SAS) were determined with alternating current voltammetry (in-phase mode) using o-nitrophenol as an electrochemical probe. A general characteristic of the SA seasonal variability for the northern Adriatic is the sinusoidal change of SA within the period of 1 year; similar behaviour was observed for the seasonal variations of temperature. Maximum SA values appeared during the summer period, while minimum SA values were measured in winter, during the period of well-mixed water layers and lower phytoplankton production. In May and October, the highest SA values were obtained in the upper seawater layer, which was ascribed to the influence of high inflow of nutrient-rich Po River freshwater. Riverine inputs indirectly favour autochthonous production processes, which result in increased concentration of organic matter (OM), particularly surface-active substances.     

An experimental study on the speciation of dissolved zinc,cadmium, lead and copper in river rhine and north sea water,by differential pulsed anodic stripping voltammetry

Dissolved electroactive concentrations of zinc, cadmium, lead and copper in river Rhine and North Sea samples have been measured at natural and lower pH values by differential pulsed anodic stripping voltammetry using a Kemula-type hanging mercury drop electrode. Average concentrations detected in North Sea samples at salinities $\text{? 32‰ S}$ and their range are (in μgl^?1): 3.9 (2.0–7.5) for zinc, 0.23 (0.13–0.31) for cadmium, 0.3 (0.1–0.6) for lead and 0.3 (0.25–0.60) for copper (pH 8.1). The APDC-MIBK extracting/concentrating method, followed by AAS measurement applied to the same samples, resulted in 3.9 (2.0–7.5) for zinc, 0.11 (0.01–0.27) for cadmium, 0.5 (0.2–0.9) for lead and 1.6 (0.7–3.2) for copper. A fraction of the electroactive concentrations at pH 2.7 (6.1 for Zn) is electroactive at pH 8.1. The fractions are 100% for Cd, 20% for Cu, 13% for Pb and 40% for Zn. The remaining fractions are partly composed of organically bound species in solution. The low value for lead may be caused by the presence of particulate lead that is dissolved at low pH.Ionic copper and lead species, added separately to seawater at pH 8.1 are removed from the electroactive form, and taken up in (organic) complexes in the same ratio (at least for copper) as the species already present. Added ionic zinc is not removed within the time scale of the measurements (30 min). North Sea water at the natural pH has a complexing capacity, probably due to the presence of dissolved organic compounds, in a concentration equivalent to 3.10^?7M copper. The complexing capacity is zero at pH 2.7. The usual method of standard addition for the determination of electroactive copper and lead concentrations may lead to erroneous results in samples where complexation of this type occurs.     

The role of surface waves in the ocean mixed layer

Previously, most ocean circulation models have overlooked the role of the surface waves. As a result, these models have produced insufficient vertical mixing, with an under - prediction of the ,nixing layer （ML） depth and an over - prediction of the sea surface temperature （SST）, particularly during the summer season. As the ocean surface layer determines the lower boundary conditions of the atmosphere, this deficiency has severely limited the performance of the coupled ocean - atmospheric models and hence the climate studies. To overcome this shortcoming, a new parameterization for the wave effects in the ML model that will correct this systematic error of insufficient mixing. The new scheme has enabled the mixing layer to deepen, the surface excessive heating to be corrected, and an excellent agreement with observed global climatologic data. The study indicates that the surface waves are essential for ML formation, and that they are the primer drivers of the upper ocean dynamics; therefore, they are critical for climate studies.     

Selected chemical contaminants in surface sediments of Commencement Bay and the Tacoma Waterways, Washington, USA

Eight metals, 21 organic priority pollutants, and 11 other contaminants and contaminant-related sediment characteristics were measured in surface sediments (upper 2 cm) at 21 locations in Commencement Bay and the Tacoma Waterways, Washington. Summary statistics were calculated and statistical approaches (analysis of variance, multiple comparisons tests, cluster analysis and principal component analysis) were applied to subsets of the data to classify sediment contamination. Overall sediment contamination was highest in the Sitcum, City and Hylebos Waterways, intermediate in Commencement Bay, at the entrances to the Tacoma Waterways and in the outer reaches of the Blair and Hylebos Waterways, and lowest at the Blair Waterway turning basin, the mouth of the Puyallup River and at a reference site near Browns Point. High concentrations of some contaminants appeared to be related to proximity to sources of contaminants. Depositional vectors, and chemical adsorption processes may also influence the spatial distribution of sediment contamination in the study area.Results of simple and partial correlation analyses indicate that arsenic, iron and manganese may be more closely associated with the clay fraction, while cadmium, copper and polynuclear aromatic hydrocarbons may be more closely associated with the total organic carbon content of sediments. We were unable to discriminate statistically between the affinity of chromium, lead, zinc and phthalates with the % clay or the total organic carbon content of sediments.     

Seasonal and spatial distribution of particulate organic matter (POM) in the Chukchi and Beaufort Seas

As part of the Western Arctic Shelf–Basin Interactions (SBI) project, the production and fate of organic carbon and nitrogen from the Chukchi and Beaufort Sea shelves were investigated during spring (5 May–15 June) and summer (15 July–25 August) cruises in 2002. Seasonal observations of suspended particulate organic carbon (POC) and nitrogen (PON) and large-particle (>53 μm) size class suggest that there was a large accumulation of carbon (C) and nitrogen (N) between spring and summer in the surface mixed layer due to high phytoplankton productivity. Considerable organic matter appeared to be transported from the shelf into the Arctic Ocean basin in an elevated POC and PON layer at the top of the upper halocline. Seasonal changes in the molar carbon:nitrogen (C:N) ratio of the suspended particulate organic matter (POM) pool reflect a change in the quality of the organic material that was present and presumably being exported to the sediment and to Arctic Ocean waters adjacent to the Chukchi and Beaufort Sea shelves. In spring, low particulate C:N ratios (<6; i.e., N rich) were observed in nitrate-replete surface waters. By the summer, localized high particulate C:N ratios (>9; i.e., N-poor) were observed in nitrate-depleted surface waters. Low POC and inorganic nutrient concentrations observed in the surface layer suggest that rates of primary, new and export production are low in the Canada Basin region of the Arctic Ocean.     

Air-sea exchange of mercury in Tokyo Bay

In Tokyo Bay the concentrations of dissolved gaseous mercury (DGM) in the surface seawater and total gaseous mercury (TGM) over the sea were measured during December 2003, October 2004 and January 2005. Based on these data, the evasional fluxes of mercury from the sea surface were estimated using a gas exchange model. In addition, an automatic wet and dry deposition sampler was used to measure the wet and dry depositional fluxes of mercury from December 2003 to November 2004 at three locations in and near Tokyo Bay. The results indicate that the average DGM and TGM levels of seven locations are 52 ± 26 ng m⁻³ and 1.9 ± 0.6 ng m⁻³, respectively, which shows that the surface seawater in Tokyo Bay is supersaturated with gaseous mercury, leading to an average mercury evasional flux of 140 ± 120 ng m⁻²d⁻¹. On the other hand, the annual average wet and dry depositional fluxes of mercury at three locations were 19 ± 3 μg m⁻²yr⁻¹ and 20 ± 9 μg m⁻²yr⁻¹, respectively. These depositional fluxes correspond to the daily average total depositional flux of 110 ± 20 ng m⁻²d⁻¹. Thus, it is suggested that in Tokyo Bay, the evasional fluxes of mercury are comparable to the depositional fluxes.     

Temporal and spatial variability of chlorophyll concentrations in the Bering Sea using empirical orthogonal function (EOF) analysis of remote sensing data

Seasonal and interannual variability of surface chlorophyll concentration in the Bering Sea was examined using Empirical Orthogonal Function (EOF) analysis of data obtained by the Sea-viewing Wide Field-of-view Sensor (SeaWiFS) from 1998 to 2002. The analysis of normalized monthly fields (removing temporal and spatial monthly means) shows that different temporal and spatial patterns are evident in the eastern and western Bering Sea during the spring bloom period. The first EOF mode explains 30% of the variability and shows how the eastern shelf break region and the western Bering Sea are out of phase during the spring bloom. The second EOF mode (17.6%) indicates a pattern involving the eastern shelf break region and the Kamchatka Basin. This strong east–west signal is linked by both surface winds and light. EOF modes of wind-speed anomalies, derived from Special Sensor Microwave Imager (SSM/I), and photosynthetically active radiance (PAR) from SeaWiFS, show a similar dipole feature where the east–west pattern is related to the position and strength of the Aleutian Low pressure system. In years when the Aleutian Low shifts from west to east, weaker wind stress facilitates the development of stratification resulting in a strong spring bloom in the western Bering Sea. The variability of spring chlorophyll has a strong connection with variability in atmospheric forcing in the Bering Sea.     

Seasonal variations of the surface currents in the Tsushima Strait

Seasonal variations of the surface currents in the Tsushima Strait were investigated by analyzing the monthly mean surface currents measured with HF radar. Several new features of the surface currents have been found. One notable feature is the large, complicated seasonal variation in the current structure in the eastern channel of the strait. For example, in the southeastern and northwestern regions of the channel, southwestward countercurrents are found in summer while southeastward acrossshore currents are found in autumn and winter. The wind-driven flow (Ekman flow) as well as surface geostrophic currents are responsible for these complicated variations of the surface currents. To quantify each variation of the flow and current, the wind-driven flow was calculated from the monthly wind (more precisely, the friction velocity) using the monthly speed factor and deflection angle estimated in our previous study, and the surface geostrophic currents were then estimated by subtracting the wind-driven flow from the measured surface currents. It was found that the acrossshore currents are the wind-driven flow, and that the surface geostrophic currents flow almost in the along-shore direction, indicating the validity of the decomposition of the surface velocity into the wind-driven flow and the geostrophic currents using the speed factor and deflection angle. A real-vector empirical orthogonal function (EOF) analysis of the surface geostrophic currents shows a pair of eddies in the lee of Tsushima and Iki Islands as the first mode, which indicates that the southwestward countercurrents in the eastern channel are formed primarily by the incoming Tsushima Warm Current.