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1.
The solubility of iron in oxic waters is so low that iron can be a limiting nutrient for phytoplankton growth in the open ocean. In order to mimic low iron concentrations in algal cultures, Ethylenediaminetetraacetate (EDTA) is commonly used. The presence of EDTA enables culture experiments to be performed at a low free metal concentration, while the total metal concentrations are high. Using EDTA provides for a more reproducible medium. In this study Fe speciation, as defined by EDTA in culture media, is compared with complexation by natural organic complexes in ocean water where Fe is thought to be limited. To grow oceanic species into iron limitation, a concentration of at least 10−4 M EDTA is necessary. Only then does the calculated [Fe3+] concentrations resemble those found in natural sea water, where the speciation is governed by natural dissolved organic ligands at nanomolar concentrations. Moreover, EDTA influences the redox speciation of iron, and thus frustrates research on the preferred source of Fe-uptake, Fe(III) or Fe(II), by algae. Nowadays, one can measure the extent of natural organic complexation in sea water, as well as the dissolved Fe(II) state, and can use ultra clean techniques in order to prevent contamination. Therefore, it is advisable to work with more natural conditions and not use EDTA to create iron limitation. This is especially important when the biological availability of the different chemical fractions of iron are the subject of research. Typically, many oceanic algae in the smallest size classes can still grow at very low ambient Fe and are not easily cultivated into limitation under ambient sea water conditions. However, the important class of large oceanic algae responsible for the major blooms and the large scale cycling of carbon, silicon and other elements, commonly has a high Fe requirement and can be grown into Fe limitation in ambient seawater.  相似文献   

2.
Abstract. The removal of glycine and glucose by freshly collected adult Mytilus edulis was determined using radiolabeled substances added to ambient concentrations of dissolved organic materials in freshly collected natural sea water. Uptake rates were calculated for substrate concentrations of 0.5 μM glycine and 1.0 μM glucose and were compared with the animals' energy and nitrogen demands as measured by oxygen consumption and ammonia excretion rates. Respiration and ammonia excretion rates as well as cither glycine or glucose removal were all determined for the same animals. The mean respiration rate was 670μl O2 g-1h-1, the mean ammonia excretion rate 1.95 μg-at NH4-g-1 h-1. The calculated uptake rates were 0.48 μmol -g-1-h-1 for free amino acids and 0.44 μmol-g-1 h-1 for free simple sugars. Such uptake rates could have contributed roughly 13% of the mussels' energy requirements or 10% of the mussels' nitrogen requirements assuming the following conditions: 0.5 μM concentration of free amino acids, 1.0μM concentration of simple sugars, uptake of total amino acids at a rate based on a weighted removal rate of glycine, alanine, serine, and glutamic acid, and uptake of simple sugars at a rate equal to that of glucose removal. It is apparent that simple organic substances dissolved in sea water may be of some benefit to mussels, especially when the substances occur in concentrations typical of coastal sea water.  相似文献   

3.
Dissolved silica can coprecipitate with zinc from seawater or distilled water that has been enriched with both elements. More than 2 ppm Si are necessary for the reaction to begin. The coprecipitation shows pH dependence. The addition of pulverized illite or natural sediment as suspended particulate material does not enhance the reaction in seawater. The organic material present in the nearshore seawater samples decreases the rate and extent of reaction, as indicated by comparisons of results of experiments using natural seawater with results obtained using UV-irradiated seawater. In unbuffered distilled water the reaction must compete with hydrolysis of zinc; however, reaction does occur, which indicates that the seawater matrix is not essential for the reaction. The coprecipitation can limit the concentration of zinc in seawater to less than the solubility concentration assumed for ZnCO3 or Zn(OH)2. The results suggest that a zinc silicate can precipitate directly from seawater or interstitial water as an authigenic mineral.  相似文献   

4.
Pentachlorophenol (PCP) and 3,4-dichloroaniline (DCA) were used as models to examine photochemical reactions in seawater.The photolysis of PCP in seawater differed in both rate and product distribution from that in distilled water; rates were slower in seawater due to the photonucleophilic interaction of PCP with chloride ions, demonstrated by the formation of 36Cl-labeled PCP in irradiated PCP solutions containing Na36Cl. DCA showed no rate change and gave identical products in both systems. Both PCP and DCA yielded greater amounts of photoreduction products in seawater than in distilled water, and tetrachloromuconic acid was isolated and identified as a new and unstable PCP photoproduct resulting from ringfission. This study demonstrates the operation of photooxidation, photonucleophilic substitution, and photoreduction reactions which differ in detail between seawater and distilled water and suggests that photochemical reactions can be a major factor in the breakdown of organic pollutants and other chemicals in the marine environment.  相似文献   

5.
A batch sorption technique for the determination of particle–water interactions of hydrophobic organic micropollutants under simulated estuarine conditions is described. Results are presented for the behaviour of 2,2′,5,5′-tetrachlorobiphenyl (2,2′,5,5′-TCB) in river and sea waters, both in the presence and absence of estuarine suspended particles. Adsorption onto particles in sea water was enhanced compared with adsorption in river water owing to salting out of the compound, and possibly of the particulate organic matter, in the presence of high concentrations of dissolved ions. The particle–water distribution coefficient, KD, decreased from about 120×103 to 10×103 ml g−1, and from about 150×103 to 20×103 ml g−1, in river water and sea water, respectively, over a particle concentration range of 10–1000 mg l−1. Incomplete recovery of compound from the reactor walls is partly responsible for a particle concentration effect, while artefacts relating to inadequate sediment and water phase separation were ruled out following further experiments. The particle concentration effect, which is replicated in many field studies of hydrophobic organic micropollutants, including 2,2′,5,5′-TCB, is incorporated into a simple partitioning model and is discussed in the context of the likely estuarine behaviour of such compounds.  相似文献   

6.
采用衍生化处理和气相色谱-质谱联用分析方法, 测定了珠江口及其以东近海海域表层海水中的三氟乙酸(Trifluoroacetic acid, TFA)含量。珠江口及其以东近岸的红海湾和大亚湾海区TFA浓度范围分别为113—170ng.L–1和202—336ng.L–1。红海湾内海水中TFA的平均水平(279ng.L–1)明显高于外海海水(210ng.L–1), 说明港湾内或其周边地区可能有TFA的点源输入。此外, 外海海水中TFA平均浓度比珠江口高69.1ng.L–1, 表明这种亲水性强、稳定性高的化合物除了已知的人为来源外, 可能还存在未知的人为源或自然源, 使得海洋作为其最终的汇浓度不断累积。  相似文献   

7.
The increasing atmospheric CO2 concentration in the last few decades has resulted in a decrease in oceanic pH. In this study, we assessed the natural variability of pH in coastal waters off Goa, eastern Arabian Sea. pHT showed large variability (7.6–8.1) with low pH conditions during south-west monsoon (SWM), and the variability is found to be associated with upwelling rather than freshwater runoff. Considering that marine biota inhabiting dynamic coastal waters off Goa are exposed to such wide range of natural fluctuations of pH, an acidification experiment was carried out. We studied the impact of low pH on the local population of sea urchin Stomopneustes variolaris (Lamarck, 1816). Sea urchins were exposed for 210 days to three treatments of pHT: 7.96, 7.76 and 7.46. Our results showed that S. variolaris at pHT 7.96 and 7.76 were not affected, whereas the ones at pHT 7.46 showed adverse effects after 120 days and 50% mortality by 210 days. However, even after exposure to low pH for 210 days, 50% organisms survived. Under low pH conditions (pHT 7.46), the elemental composition of sea urchin spines exhibited deposition of excess Sr2+ as compared to Mg2+ ions. We conclude that although the sea urchins would be affected in future high CO2 waters, at present they are not at risk even during the south-west monsoon when low pH waters reside on the shelf.  相似文献   

8.
南沙群岛海区有机碳沉积作用与古生产力估算   总被引：1，自引：0，他引：1  
根据南沙群岛海区５个沉积柱样和大量表层样的分析资料讨论了有机碳的沉积作用。深海有机碳含量一般为０．２％－１．３％。水柱深度对其分布的控制作用不明显。分析结果发现冰期、间冰期，尤其是本次冰期有机碳含量变化明显，４个柱样晚第四纪的质量堆积速率在末次冰期时最大。有机碳保存的主要控制因素是溶解氧浓度、粘土矿物含量、水柱深度和底栖混合强度，其中溶解氧浓度是最重要因素。底栖有孔虫的相对丰度，如Ｕｖｉｇｅｒｉｎａ和Ｂｕｌｉｍｉ－ｎａ，可用来指示溶解氧和有机碳含量。有机碳含量与海洋生产力关系极为密切，它可用来重建海洋古生产力的长期变化。采用Ｍｌｌｅｒ和Ｓｕｅｓｓ方程以及Ｓａｒｎｔｈｅｉｎ方程的计算结果与目前生产力值结果比较表明，后一种方法因充分考虑了溶解氧浓度和水柱深度而更接近现代值。  相似文献   

9.
In order to investigate the photobleaching potential of estuarine waters from different depths and redox conditions and with varying degree of biological activity, filtered, unfiltered and chloroform-poisoned water samples from the Baltic Sea were exposed to ambient sunlight. Fluorescence, at excitation 350 nm and emission 450 nm, was used as an indication of humic substance concentration. Fluorescence and organic carbon concentration were measured at regular time intervals during light exposure. We found that the decrease in humic substance fluorescence can be fitted to an exponential decay function. The fluorescence half-lives were within the range 0.4 – 4.6 days in different water masses, with fluorescence decreasing to between 20% and 60% of initial concentration, respectively. Results from the curve fitting procedure indicate a rest concentration of humic substance fluorescence, similar among the sampled sites, that is resistant to further photochemical degradation. The largest relative decreases in fluorescence were found in deep waters, but samples from deep waters also had a higher fluorescence rest concentration than samples from surface waters. Biological activity was reduced by filtering the samples through 0.2μm pore size filters or adding chloroform. No statistically significant differences were found after 3 days of irradiation between samples with and without treatment to reduce biological activity. The highest initial fluorescence values and the largest fluorescence decrease were found in the anoxic waters of the Gotland Deep. The organic carbon concentrations decreased 3–7% at all stations. The shortest half-life of humic substance, and the largest decrease in organic carbon concentrations, were found in samples from the northern basins of the Baltic Sea.  相似文献   

10.
Actinide speciation in aquatic systems   总被引：1，自引：0，他引：1  
Nuclear test explosions and reactor wastes have deposited an estimated 16 × 1015 Bq of plutonium into the world's aquatic systems. However, plutonium concentration in open ocean waters is on the order 10− 5 Bq/kg, indicating that most of the plutonium is quite insoluble in marine waters and has been incorporated into sediments. Actinide ions often are not in a state of thermodynamic equilibrium and their solubility and migration behavior is related to the form in which the nuclides were introduced into the aquatic system.Actinide solubility depends on such factors as the pH (hydrolysis), Eh (oxidation state), reaction with complexants (e.g., carbonate, phosphate, humic acid, etc.), sorption to surfaces of minerals and/or colloids etc., in the water. The most significant of these variables is the oxidation state of the metal ion. The simultaneous presence of more than one oxidation state for some actinides (e.g., plutonium) in a solution complicates actinide environmental behavior. Both Np(V)O2+ and Pu(V)O2+, the most significant states in natural, oxic waters are relatively noncomplexing and resistant to hydrolysis and subsequent precipitation. The solubility of NpO2+ can be as high as 10− 4 M while that of PuO2+ is limited by reduction to the insoluble tetravalent species, Pu(OH4), (pKsp = 56). The net solubility of hexavalent UO22+ in sea water is also limited by hydrolysis; however, it has a relatively high concentration due to formation carbonate complexes. The insoluble trivalent americium hydroxocarbonate, Am(CO)3(OH), is limiting species for the solubility of Am(III) in sea water. Thorium is found exclusively as the tetravalent species and its solubility is limited by the formation of quite insoluble Th(OH)4.The chemistry of actinide ions in the environment is reviewed to show the spectrum of reactions that can occur in natural waters which must be considered in assessing the environmental behavior of actinides. While much is understood about sorption of actinides on surfaces, the mode of migration of actinides in such waters and the potential effects of these radioactive species on marine bioto, much more is needed for a satisfactory understanding of the behavior of the actinides in the environment.  相似文献   

11.
In this paper SIT and Pitzer models are used for the first time to describe the interactions of natural and synthetic polyelectrolytes in natural waters. Measurements were made potentiometrically at 25 °C in single electrolyte media, such as Et4NI and NaCl (for fulvic acid 0.1 < I /mol L− 1 < 0.75), and in a multi-component medium simulating the composition of natural waters at a wide range of salinities (for fulvic and alginic acids: 5 < S < 45) with particular reference to sea water [Synthetic Sea Water for Equilibrium studies, SSWE]. In order to simplify calculations, SSWE was considered to be a “single salt” BA, with cation B and anion A representing all the major cations (Na+, K+, Mg2+, Ca2+) and anions (Cl−, SO42−) in natural sea water, respectively. The ion pair formation model was also applied to fulvate and alginate in artificial sea water by examining the interaction of polyanions with the single sea water cation. Results were compared with those obtained from previous speciation studies of synthetic polyelectrolytes (polyacrylic and polymethacrylic acids of different molecular weights). Results indicate that the SIT, Pitzer and Ion Pairing formation models used in studies of low molecular weight electrolytes may also be applied to polyelctrolytes with a few simple adjustments.  相似文献   

12.
The speciation of sedimentary sulfur (pyrite, acid volatile sulfides (AVS), S0, H2S, and sulfate) was analyzed in surface sediments recovered at different water depths from the northwestern margin of the Black Sea. Additionally, dissolved and dithionite-extractable iron were quantified, and the sulfur isotope ratios in pyrite were measured. Sulfur and iron cycling in surface sediments of the northwestern part of the Black Sea is largely influenced by (1) organic matter supply to the sediment, (2) availability of reactive iron compounds and (3) oxygen concentrations in the bottom waters. Biologically active, accumulating sediments just in front of the river deltas were characterized by high AVS contents and a fast depletion of sulfate concentration with depth, most likely due to high sulfate reduction rates (SRR). The δ34S values of pyrite in these sediments were relatively heavy (−8‰ to −21‰ vs. V-CDT). On the central shelf, where benthic mineralization rates are lower, re-oxidation processes may become more important and result in pyrite extremely depleted in δ34S (−39‰ to −46‰ vs. V-CDT). A high variability in δ34S values of pyrite in sediments from the shelf-edge (−6‰ to −46‰ vs. V-CDT) reflects characteristic fluctuations in the oxygen concentrations of bottom waters or varying sediment accumulation rates. During periods of oxic conditions or low sediment accumulation rates, re-oxidation processes became important resulting in low AVS concentrations and light δ34S values. Anoxic conditions in the bottom waters overlying shelf-edge sediments or periods of high accumulation rates are reflected in enhanced AVS contents and heavier sulfur isotope values. The sulfur and iron contents and the light and uniform pyrite isotopic composition (−37‰ to −39‰ vs. V-CDT) of sediments in the permanently anoxic deep sea (1494 m water depth) reflect the formation of pyrite in the upper part of the sulfidic water column and the anoxic surface sediment. The present study demonstrates that pyrite, which is extremely depleted in 34S, can be found in the Black Sea surface sediments that are positioned both above and below the chemocline, despite differences in biogeochemical and microbial controlling factors.  相似文献   

13.
The relation between the nitrate and phosphate concentrations in the Sea of Okhotsk and the bordering waters of the Pacific Ocean were studied. The surveys were carried out in the autumn, spring, and summer of 2001–2002. For the deepwater part of the sea, the relation [NO? 3] = ((14.88 ± 0.07) × [PO3? 4] ? 5.46 ± 0.17) was found. The coefficients in the equation given are statistically different from those in the similar equation for the Pacific waters: [NO? 3] = (16.05 ± 0.15) × [PO3? 4]-(7.23 ± 0.36). In the northern part of the sea; on the shelf; in the slope area; and, especially, in the deep waters of the TINRO Depression, the linear dependence between the phosphate and nitrate concentrations was distorted. This feature was described in terms of nitrate deficiency. The maximum values of this deficiency were found in the near-bottom waters. The principal processes that might cause the nitrate deficiency were considered: the difference in the oxidation rates of the nitrogen and phosphorus organic compounds, the matter transfer between the continent and the sea, the different efficiency of the biogenic burial of nitrogen and phosphorus in the bottom sediments, and the denitrification in the upper layer of the bottom sediments. It was shown that the most probable cause of the nitrate deficiency was the denitrification. The loss of inorganic nitrogen owing to the supply of the waters of the Sea of Okhotsk to the Pacific Ocean was estimated as ～2.5 × 1011 mol N/year.  相似文献   

14.
We found similar microbial degradation rates of labile dissolved organic matter in oxic and suboxic waters off northern Chile. Rates of peptide hydrolysis and amino acid uptake in unconcentrated water samples were not low in the water column where oxygen concentration was depleted. Hydrolysis rates ranged from 65 to 160 nmol peptide L−1 h−1 in the top 20 m, 8–28 nmol peptide L−1 h−1 between 100 and 300 m (O2-depleted zone), and 14–19 nmol peptide L−1 h−1 between 600 and 800 m. Dissolved free amino acid uptake rates were 9–26, 3–17, and 6 nmol L−1 h−1 at similar depth intervals. Since these findings are consistent with a model of comparable potential activity of microbes in degrading labile substrates of planktonic origin, we suggest, as do other authors, that differences in decomposition rates with high and low oxygen concentrations may be a matter of substrate lability. The comparison between hydrolysis and uptake rates indicates that microbial peptide hydrolysis occurs at similar or faster rates than amino acid uptake in the water column, and that the hydrolysis of peptides is not a rate-limiting step for the complete remineralization of labile macromolecules. Low O2 waters process about 10 tons of peptide carbon per h, double the amount processed in surface-oxygenated water. In the oxygen minimum zone, we suggest that the C balance may be affected by the low lability of the dissolved organic matter when this is upwelled to the surface. An important fraction of dissolved organic matter is processed in the oxygen minimum layer, a prominent feature of the coastal ocean in the highly productive Humboldt Current System.  相似文献   

15.
As a part of the JGOFS synthesis and modeling project, researchers have been working to synthesize the WOCE/JGOFS/DOE/NOAA global CO2 survey data to better understand carbon cycling processes in the oceans. Working with international investigators we have compiled a Pacific Ocean data set with over 35,000 unique samples analyzed for at least two carbon species, oxygen, nutrients, chlorofluorocarbon (CFC) tracers, and hydrographic parameters. We use these data here to estimate in-situ oxygen utilization rates (OUR) and organic carbon remineralization rates within the upper water column of the Pacific Ocean. OURs are derived from the observed apparent oxygen utilization (AOU) and the water age estimates based on CFCs in the upper water and natural radiocarbon in deep waters. The rates are generally highest just below the euphotic zone and decrease with depth to values that are much lower and nearly constant in water deeper than 1200 m. OURs ranged from about 0.02–10 μmol kg−1yr−1 in the upper water masses from about 100–1000 m, and averaged = 0.10 μmol kg−1yr−1 in deep waters below 1200 m. The OUR data can be used to directly estimate organic carbon remineralization rates using the C:O Redfield ratio given in Anderson and Sarmiento (1994). When these rates are integrated we obtain an estimate of 5.3 ± 1 Pg C yr−1 for the remineralization of organic carbon in the upper water column of the Pacific Ocean. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

16.
Compositions and fluxes of amino acids and major chloropigments were measured in the central equatorial Pacific Ocean as part of the US JGOFS EqPac program. Fluxes decreased by several orders of magnitude, from 400 to 0.03 mg amino acid m−2 d−1 and from 9 mg to 0.0004 μg chloropigment m−2 d−1, between production in the surface waters and accumulation at the sea floor. Most rapid losses were in surface waters and at the sediment interface. Losses from the mid-water column were as great as those in surface waters or at the sediment interface, but occurred over a much greater depth range. Export flux estimates based on floating sediment traps were higher near the equator and decreased poleward, similar to primary production.Little meridional difference was apparent in composition of either amino acids or pigments in exported material over the 24° of latitude sampled in spite of the large (factor of 5–6) difference in fluxes. However, pigment composition changed dramatically with depth in the water column, and considerable diagenesis occurred before particles reached the sediment. Pigment compositions suggest that suspended particles were more degraded in the northern than in the southern hemisphere, possibly due to differences in food chain structure. Compositional changes in amino acids occurred in the water column, but were most noticeable at the sediment–seawater interface. Increases in the relative proportions of aspartic acid and glycine with depth were more consistent with preferential preservation within the particulate matrix than with any inherent stability of these compounds to heterotrophic consumption. The contribution of amino acids and pigments to total organic carbon clearly shows that selective degradation of organic matter occurs with depth; this is not evident from total organic carbon data alone. Amino acids contributed about a quarter of the total organic carbon (OC) in surface waters and 16% of the OC in sediment; pigments decreased from 1% of total OC in surface waters to <0.001% in sediments. Decreases in the contribution of amino acids to total organic carbon may be due to transformation into uncharacterizeable material as well as to respiration.  相似文献   

17.
Under the artificial condition the 59Fe morphology in sea water, its concentration in sediment and phytoplankton, its distribution and metabolism in tissue organs of marine animals were studied. The results showed that the morphology of 59Fe was in a particulate state in sea water. The adsorption rule of 59Fe by three kinds of sediments was similar. The concentration ability of 59Fe by phytoplankton was very strong. The critical concentration organs of S9Fe by marine animals were viscera. The gross radioactivity of 59Fe was mainly concentrated in protein. The concentration factor of 59Fe by DNA was the highest one. After excretion experiment, 59Fe of all the tissue organs was not detected. Small part of59Fe remained in the organic acid and protein state. There was a redistribution process in sediment for59Fe.  相似文献   

18.
The spectral measurements of the attenuation coefficient of sea water and the absorption coefficient of suspended particles and of yellow substance were made with a spectrophotometer for the sea waters sampled in Tokyo Bay. These parameters can be used to compute the expected spectral irradiance reflectance. Some relationships between the optical properties of sea water and the concentration of dissolved organic carbon, the dry weight of suspended matter and chlorophyll-a concentration are presented. On the basis of these results, the possibility of modelling the relationship between optical and material properties is discussed.  相似文献   

19.
Since 1960 when I was a senior student, I have studied natural phenomena observed in the hydrosphere and atmosphere by means of chemical elements. Each of the phenomena is, in general, very complicated and so I have attempted to depict the whole picture of material circulation in the marine environment by studying its various aspects at the same time. My chief strategy has been to use natural radio-nuclides as clocks of various phenomena, and to use sediment traps for the determination of vertical fluxes in the ocean. The many results I have obtained can be summarized as follows. 1. I have found that several sporadic events control the material exchange through the atmosphere. These include the strong winter monsoon and typhoons that transport sea-salt particles to the Japanese Islands, theKosa episodes that transport soil dust to the ocean, and storms that result in exchange of sparingly soluble gases such as oxygen and carbon dioxide at the air-sea interface. I have also proved quantitatively that the source of aluminosilicate material in pelagic sediments is air-borne dust. 2. I have proposed a model,Settling model, for the removal of chemical substances from the ocean and found various lines of evidence supporting the model. This model predicts the reversibility in the existing state of insoluble chemical elements in seawater among large settling particles, small suspended particles and colloidal particles that pass through a membrane filter and explains well their behavior in the ocean. I have first precisely measured calcium and iodine in the ocean and have explained their distributions on the basis of the solution and redox equilibria. 3. Using chemical tracers, I have estimated the vertical eddy diffusion coefficients to be 1.2 cm2sec−1 for the Pacific deep water, 0.5 cm2sec−1 for the deep Bering Sea water and 3–80 cm2sec−1 for the Pacific surface water, and have studied the structure of water masses in the western North Pacific and the Sea of Japan. I have also invented and applied a method for the calculation of the age of deep waters using radiocarbon. 4. I have calculated the rates of decomposition of organic matter and the regeneration rates of chemical components in the deep and bottom waters as well as coastal waters by modelling water circulation and mixing. Particulate fluxes and regeneration rates are larger in the deep waters beneath the more biologically productive surface waters. I have stressed the role of silicate in the marine ecosystem, especially in the succession of phytoplankton species. 5. I have quantitatively studied the migration of chemical elements during the early diagenesis of bottom sediments especially manganese using chemical and radiochemical techniques. Manganese is being actively recycled not only in coastal seas but also in pelagic sediments except in the highly oligotrophic subtropical ocean. This recycling can explain the formation of manganese nodules and enables us to balance the manganese budget in the ocean.  相似文献   

20.
The concentration of 15 amino acids in hydrolyzed particulate matter from different regions and depths of the Pacific Ocean has been measured by gas—liquid chromatography. The relative composition was similar for all samples in the euphotic zone, where the particulate amino acid (PAA) concentration ranged from 370 to 2260 nmoles/1 in coastal waters and from 90 to 260 nmoles/1 in the open ocean. Total PAA concentration dropped rapidly with depth, levelling off at 10–40 nmoles/1 below 200 m. Glycine, serine, glutamic acid and aspartic acid were the most abundant PAA in deep equatorial water and in deep off-shore California water. The nitrogen content of PAA could often account for 100% of the total particulate organic nitrogen present, while PAA carbon contributed up to 50% of the total particulate organic carbon in euphotic waters and down to 20% in deep waters. The protein equivalent to the total PAA content of particulate matter in near-surface waters amounted to 11–32 μg/1 at oceanic stations and up to 270 μg/1 at coastal stations.  相似文献   

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