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1.
用高效液相色谱法对2010年9月南黄海33个站位表层海水中总水解氨基酸(THAA)、溶解游离氨基酸(DFAA)、溶解结合氨基酸(DCAA)的分布、组成以及它们与环境因子的相关性进行了研究。结果表明:THAA平均浓度为2.08μmol/L,DFAA平均浓度为0.39μmol/L,DCAA平均浓度为1.69μmol/L。THAA浓度的分布大致呈近岸高、远岸低的特点;DFAA分布的规律性较差,在东部海域(中心约在35°N,123°E)出现高值。相关性分析显示溶解氨基酸与叶绿素a(Chl-a)、溶解无机氮(DIN)、细菌丰度、温度和盐度之间均无显著相关性。THAA中含量较高的个体氨基酸为丝氨酸、甘氨酸、天门冬氨酸、谷氨酸和丙氨酸,总和占70.59%。DFAA、DCAA中的主要成分与THAA基本相同。THAA中个体氨基酸的组成以34°N为界分为南北2个海区呈现明显的区域性特点。  相似文献   

2.
In this study, we present seasonal changes (monthly samples from September 2001 to August 2003) in the abundance and composition of dissolved and particulate amino acids, at one station in the lower Mississippi and Pearl Rivers (LA, MS: USA). Spatial changes over a 4-day transmit from river km 390 to river mouth (Head of Passes, LA) in the Mississippi River, and a two-day downstream sampling from Jackson (MS) to Stennis Space Center (MS) were also determined. Temporal data in the lower Mississippi River showed significantly lower concentrations of dissolved combined amino acids (DCAA, 0.8 to 2.2 μM) and dissolved amino acids in high molecular weight fraction (HMW DAA, 0.2–0.4 μM) than in the Pearl River (DCAA, 1.4–4.3 μM; HMW DAA, 0.4–1.4 μM). Dissolved free amino acids (DFAA) were significantly lower than DCAA in both rivers, and displayed minimal seasonal variability. DCAA, HMW DAA, and particulate amino acids (PAA) were generally higher during high-flow periods, which may have suggested dominance in terrestrial sources. Carbon-normalized yield of PAA (%C-PAA) was generally higher during low-flow conditions and positively correlated with chlorophyll-a (chl-a), reflective of in situ sources. Downstream variability in the lower Mississippi River showed stable DCAA concentrations, a decline in PAA (from 1.06 to 0.43 μM), and a gradual increase in mole percent of non-protein amino acids (%NPAA). This likely reflected bacterial degradation of phytoplankton biomass during falling discharge. Nitrogen-normalized yield of PAA (%N-PAA) was inversely correlated with PAA (R = − 0.7, n = 48), indicative of short-term sedimentation and resuspension events. Conversely, downstream decreases in DCAA and middle-reach peaks of PAA and %N-PAA in the Pearl River, likely resulted from photochemical degradation of DOM as well as algal production during base-flow conditions. The comparisons in abundance and composition of DAA and PAA in these different river systems provides important information on in situ nitrogen and carbon cycling as related to riverine inputs of organic matter to coastal ocean.  相似文献   

3.
Concentrations of particulate Fe, Mn, Ni, Cu, Zn, Cd and Pb have been measured in surface microlayer and subsurface seawater samples collected in the North Sea adjacent to the East Anglian coast, in an area subject to a considerable fluvial input of clay minerals. The results are interpreted by estimating the magnitudes of different processes affecting particulate matter in the microlayer: atmospheric deposition, Brownian diffusion, gravitational settling, bubble flotation and mixing. Both Fe and Mn are strongly depleted in the microlayer, evidently as a result of gravitational settling of Fe- and Mn-bearing mineral particles out of the microlayer. These particles are mixed into the surface region from the water column beneath. Microlayer enrichment of Cu, Zn and Pb was also observed and probably results from flotation of particles attached to rising bubbles. In one set of samples, however, the marked enrichment of these elements, as well as Ni, may result instead from deposition of particles from the atmosphere directly onto the water surface.  相似文献   

4.
The method of Parsonset al. (1984) for measuring dissolved free amino acids (DFAA) in coastal seawater was modified. We found considerable interference in DFAA determination from ammonia dissolved in coastal seawater, although the interference of urea could be ignored. For DFAA analysis for coastal seawater samples, ammonia determinations for the same sample are needed to correct DFAA values. For coastal surface seawater samples from all over the Seto Inland Sea, Japan, values of DFAA ranged from undetectable to 1.87 μg-at N/l when corrected for ammonia, while uncorrected values ranged from undetectable to 2.61 μg-at N/l. DFAA, urea, nitrate+nitrite, ammonia and DON concentrations in surface seawater collected in the Seto Inland Sea were analyzed simultaneously. DFAA at four seasons constituted from 1.4 to 10.1% of DON, with a mean value of 6.5%. The concentration of urea was similar to that of DFAA and often higher than that of ammonium, although generally lower than that of nitrate.  相似文献   

5.
Abstract. Dissolved free amino acids (DFAA) were measured in sediment porewater and overlying sea water in seagrass beds of Posidonia oceanica and Cymodocea nodosa at a water depth of 8–10 m in Corsica, France. In the sea water, DFAA concentrations from 0.5 to 1.9μM were found. Lowest concentrations occurred in the afternoon in surface water samples, while higher concentrations were measured in morning surface samples and in all bottom samples. The most abundant amino acids were serine, glycine, and alanine. In the sediment, the upper 4cm contained the highest concentrations of DFAA (177nmol cm-3 or 367 μM), while lower concentrations (<50nmol cm-3 or 104 μM) prevailed deeper in the sediment. Glycine, glutamic acid, alanine, and β-alanine were the major components of the DFAA. The photosynthetic activity of the seagrasses influenced sediment porewater pools of DFAA. When a Posidonia bed was covered with a black polyethylene shield, the interstitial amino acids were reduced at a rate of 16nmol cm-2 h-1 (0-10cm depth). Conversely, extended daylight (floodlight) increased the DFAA pool in sediment depths below 4 cm. Free amino acids were released to the overlying sea water from both seagrass sediment and individual shoots, the rates being highest in the dark. The present investigation indicates that a substantial portion of the N-cycling of the seagrass sediment includes free amino acids.  相似文献   

6.
Detailed sampling of the water column and subsequent high-resolution gas chromatographic analyses of surface film, particulate and dissolved hydrocarbons from the Georges Bank region off the New England coast have revealed large spatial and temporal heterogeneity in the source of hydrocarbons. Dissolved hydrocarbons, largely of a petroleum-related origin, surface film hydrocarbon also of a petroleum-related origin but different from the dissolved fraction, and bulk-water particulate matter of a mixed biogenic and petrogenic origin are all decoupled with respect to source and quantity in the region.Surface film (microlayer) hydrocarbons are found in greater concentrations than the dissolved fraction, which in turn is greater than the particulate hydrocarbon quantities in the water column. Although the microlayer appears enriched in hydrocarbons relative to the bulk water, the nature of the hydrocarbons is quite different, indicating that the use of a microlayer enrichment factor may not be appropriate in these waters.  相似文献   

7.
A seasonal study on coastal microplankton was conducted in surface waters near Boothbay Harbor, Maine. Phytoplankton biomass, particulate production and extracellular organic release were examined in conjunction with microheterotrophic biomass and the uptake and respiration of amino acids. In situ dissolved free amino acid (DFAA) concentrations were also determined. Several phytoplankton blooms occurred throughout the year, in mid-summer, late autumn and in mid-winter. Heterotrophic activity and biomass paralleled phytoplankton extracellular release more closely than either phytoplankton particulate production or biomass. DFAA concentrations were not wholly dependent on extracellular release. Heterotrophic uptake did not appear to be dependent on DFAA concentrations but rather on rates of production of DOC by phytoplankton.  相似文献   

8.
《Marine Chemistry》2001,73(3-4):319-332
The accumulation of dissolved organic matter (DOM) at the air–sea interface is controlled by dynamic physical processes at the boundary between ocean and atmosphere. Much of the DOM concentrated in the surface microlayer is thought to be protein or glycoprotein. Enzymatic hydrolysis of these and other biopolymers is an important step in the microbial uptake of dissolved and particulate organic matter in many aquatic environments. We employed a sensitive fluorescence technique to investigate differences between extracellular enzymatic peptide hydrolysis in the sea surface microlayer and corresponding subsurface water from Stony Brook Harbor, NY. We separated the microlayer from its underlying water and thus measured hydrolysis potential rather than an in-situ process. Peptide turnover was always faster in the microlayer than in subsurface waters. This was confirmed by allowing a new surface film to form on subsurface water; hydrolysis was still faster in the new surface film. In a year-long study, we found the relative difference between turnover times in the surface film and subsurface waters to vary greatly with season. While rate constants of peptide hydrolysis were generally higher in both microlayer and bulk water samples in spring/summer than in fall/winter, the difference in activity between the two environments was greatest in winter. Enhanced hydrolysis in the sea surface microlayer is likely due to the greater concentrations of DOM in the microlayer. Seasonal changes in distribution of hydrolytic activity between surface film and subsurface water probably reflect seasonal variation in the mechanisms of DOM enrichment, which depend on water temperature, substance and energy fluxes across the water–air boundary, activity of aquatic organisms and other seasonal variables.  相似文献   

9.
The accumulation of phytoplankton biomass in recurring summer dinoflagellate blooms of Chesapeake Bay is accompanied by large pools of dissolved organic matter (DOM). Two fractions of the DOM, free amino acids (DFAA) and monosaccharides (MONO), were measured at 3 h intervals in mixed species dinoflagellate blooms (Katodinium rotundatum, Gymnodinium spp.) and related to productivity, biomass and photoperiod. Peak chlorophyll levels for the three blooms were 28, 65 and 938 μg1−1. In general, DFAA and MONO concentrations increased with increasing biomass of bloom-forming species, reaching 203 and 844 μg1−1. MONO appeared to accumulate during the day while there was no consistent pattern for DFAA. The accumulations of DFAA and MONO in blooms indicate that bloom production might stimulate microheterotrophy, thereby enhancing carbon and nutrient cycling in bloom-impacted regions.  相似文献   

10.
《Marine Chemistry》1987,22(1):13-30
The composition and bacterial utilization of dissolved free amino acids (DFAA) in tropical mangrove sediments was examined. Amino acid concentrations (300–900 ng total DFAA ml−1) and composition were similar to that of other organic-rich, anaerobic sediments with lowest and highest concentrations in the low and mid intertidal zones, respectively. The non-protein amino acid, β-glutamic acid, rarely reported in previous studies, was found as a major component of the interstitial DFAA pool. Intracellular amino acids from some cultured strains of sulphate-reducing bacteria (e.g. Desulfobacter app) showed the presence of β-glutamic acid as a major cellular constituent suggesting that these bacteria may be a source of this amino acid in mangrove pore waters. In high intertidal sediments, bacterial growth rates (μ) correlated significantly with total DFAA concentrations with depth.Amino acid concentrations and composition differed significantly between sediments and overlying tidal waters. Flux chamber experiments showed negligible amino acid flux out of the sediments in untreated chambers, but rates of amino acid flux ranged from 27 to 69 mgN m−2 day−1 (= 81–207 mg C.m−2 day−1) in chambers where poisons were applied to the sediment surface. Such fluxes could account for between 9–38% and 5–19% of the nitrogen and carbon required to support the levels of bacterial productivity measured in surface (0–1 cm) sediments. These experiments suggest that bacterial populations in surface sediments are capable of utilizing all of the amino acid flux to the sediment-water interface in tropical mangroves.  相似文献   

11.
-The enrichment of nutrients (NOa-, NOa-, PO43-), suspended particles, organic matter (POC, PON,DOC) , and trace metals (Cu, Ni, Cd) was determined in the sea surface microlayer of Xiamen Bay and Jiulong Estuary. The mean enrichment factors ([Xi]microlayer/[Xi ]15cm in depth) mostly ranged between 1 . 0 and 2. 0. The dissolved forms were the major forms of the components measured, the enrichment of dissolved organic matter and suspended particles could lead to the changes in the total amount and speciation of nutrients and trace metals. No correlation was observed between sample concentrations, speciation, enrichment factors and sample locations. However, some evidence shows that these parameters are correlated with sea state, indicating the complexity and dynamic nature of the sea surface microlayer.  相似文献   

12.
The effects of the bubble breaking process on the atmospheric geochemical cycles of the elements Fe, Cu and Zn were investigated, in situ, in the estuarine waters of Narragansett Bay, Rhode Island. Enrichment, as defined by the metal-to-sodium ratios in the aerosols produced compared to their ratio in bulk water, occurred for the three metals investigated. The extent and potential geochemical importance of the process were different for each element. Iron enrichment was quite low (enrichment factor (EF) <100) and constant, and scavenging of iron from the water column and subsequent enrichment on the aerosols produced did not appear to occur. Copper enrichment on the aerosols was 200 and appeared to be influenced by both microlayer and scavenging effects. In addition, copper enrichment appears to be correlated to biological processes. Zinc enrichment was approximately the same as Cu; however, a strong scavening effect appeared to occur, suggesting scavenging of Zn by rising bubbles. Scavenging effects suggest that open-ocean enrichments for Cu may be slightly higher than observed here and a great deal higher for Zn.Geochemical implications of the data, together with other existing data, indicate that the sea is an insignificant source of Fe to the atmosphere. The sea may be a significant source (contributing on the order of 10% or more) of the total annual quantity of Cu and Zn to the atmosphere.  相似文献   

13.
Improved methodology for amino acid analysis coupled with semi-micro isolation techniques make feasible the measurement of individual amino acids from marine waters where sample volumes are limited (e.g., sediment pore water or culture filtrates). If a water sample contains more than 20 nmole 1?1 of the respective compounds, dissolved free amino acids (DFAA) can be isolated from 5 ml of filtrate by cation exchange and measured on a sensitive amino-acid analyzer equipped with a fluorometric detector. Two ml generally provides sufficient sample to determine total dissolved amino acids. Lower concentrations of amino acids can be measured after concentration from larger samples (250 ml) by ligand exchange.  相似文献   

14.
小角刺藻生长过程中溶解游离氨基酸含量在海水中的变化   总被引：2，自引：1，他引：2  
于1986年12月-1987年2月在温度为25±1℃下培养小角刺藻，以HPLC法测定该藻在培养过程中海水的溶解游离氨基酸（DFAA）含量变化。结果表明，小角刺藻不仅是海水中DFAA的主要生产者，而且也是DFAA的消耗者。小角刺藻不仅在缺乏硝酸盐的时候要吸收DFAA，即使在硝酸盐充足的情况下也会吸收。在小角刺藻的生长初期，水体中DFAA的含量迅速降低，而在后期却又大大增高。在小角刺藻的不同生长阶段，水体中DFAA的组成也不同。这些都可以说明海洋中DFAA的含量、组成和地区分布是密切地同浮游植物群落的繁殖消亡过程相关联的。  相似文献   

15.
The objectives of this study were to investigate the seasonality, abundance, sources and bioreactivity of organic matter in the water column of the western Arctic Ocean. The concentrations of particulate and dissolved amino acids and amino sugars, as well as bulk properties of particulate and dissolved organic matter (DOM), were measured in shelf, slope and basin waters collected during the spring and summer of 2002. Particulate organic matter concentrations in shelf waters increased by a factor of 10 between spring and summer. Dissolved organic carbon (DOC) and nitrogen (DON) concentrations exhibited only minor seasonal variations, whereas dissolved amino acid concentrations doubled between spring and summer, and dissolved amino sugars increased by 31% in shelf waters of the Chukchi and Beaufort Seas. Concentrations of DOC did not exhibit a significant seasonal change in surface waters of the Canada Basin, but dissolved amino acid concentrations increased by 45% between spring and summer. No significant seasonal differences were detected in the concentration or composition of DOM in waters below 100 m in depth. Concentrations of particulate and dissolved amino acids and amino sugars were strongly correlated with chlorophyll-a, indicating a plankton source of freshly produced organic matter. The amino acid and amino sugar compositions of freshly produced DOM indicated that a large portion of this material is bioavailable. While freshly produced DOM was found to be relatively bioreactive, preformed DOM in the Arctic appears to be less bioreactive but similar in degradation state to average DOM in the Atlantic and Pacific. These data demonstrate substantial summer production of POM and DOM on the Chukchi and Beaufort shelves that is available for utilization in shelf waters and export to the Canada Basin.  相似文献   

16.
Three outdoor plastic tanks were filled with North Sea water. The water was filtered free of algae and inoculated with the diatom Thalassiosira rotula. Under nearly natural nutrient supply an exponential plankton growth occurred with realistic cell concentrations. The flexible tanks (3–4 m3, 4–5 m deep) were exposed in the German Bight at a station in the outer harbour of Helgoland. The concentration changes of dissolved free amino acids (DFAA) were determined. The direct determination method applied permitted an analysis in picomole range without loss and with good reproducibility. The preliminary concentration of DFAA amounted to 0.2 μmol dm−3 in all three cultures, increasing during the development of T. rotula to 0.9–1.3 μmol dm−3 and decreasing in the stationary phase back again to smaller values. A high degree of temporal variation in DFAA was observed in all three cultures. In spite of these rapid changes in concentration, a good parallel development could be shown for all cultures, which extended as far as the spectra of the amino acids. Relationships between DFAA and other parameters of the culture-systems were examined.  相似文献   

17.
Sixteen surface microlayer samples and corresponding subsurface water samples were collected in the western North Atlantic during April–May 2003 to study the distribution and cycling of dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) and the factors influencing them. In the surface microlayer, high concentrations of DMS appeared mostly in the samples containing high levels of chlorophyll a, and a significant correlation was found between DMS and chlorophyll a concentrations. In addition, microlayer DMS concentrations were correlated with microlayer DMSPd (dissolved) concentrations. DMSPd was found to be enriched in the microlayer with an average enrichment factor (EF) of 5.19. However, no microlayer enrichment of DMS was found for most samples collected. Interestingly, the DMS production rates in the microlayer were much higher than those in the subsurface water. Enhanced DMS production in the microlayer was likely due to the higher concentrations of DMSPd in the microlayer. A consistent pattern was observed in this study in which the concentrations of DMS, DMSPd, DMSPp (particulate) and chlorophyll a in the microlayer were closely related to their corresponding subsurface water concentrations, suggesting that these constituents in the microlayer were directly dependent on the transport from the bulk liquid below. Enhanced DMS production in the microlayer further reinforces the conclusion that the surface microlayer has greater biological activity relative to the underlying water.  相似文献   

18.
Although seawater concentration of tributyltin (TBT) should decrease when the direct inputs from ship hulls will cease after the incoming world ban of organotin-based antifouling paints in 2003 or later, the TBT environmental issue will still be present for decades as contaminated sediments in shallow waters will be acting as a long-lasting reservoir for TBT and its degradation products. The lost of TBT to the atmosphere by volatilization has already been proposed as a part of its molecular motion through the aquatic environment but most recent calculated values of water-to-air rate of exchange of TBT (from 20 to 510 nmol m−2 year−1) do not take into account the potential contribution of aerosols ejection to the atmosphere upon bubbles bursting, an important process for pollutants transport in the marine environment. In this work, an experimental approach to measure the seawater-to-air flux of TBT mediated by bubbles bursting is described, and the influence of phytoplankton cells and dissolved organic matter from exudates and culture weathering on flux rates was assessed. The results demonstrate that TBT can be transferred from water to air via the ejection of droplets from bubbles bursting and that cell density strongly affected the transfer. Under a bubbling regime, the water-to-air flux (pmol TBT cm−2 min−1 level) is estimated up to 1000-fold the flux measured for the molecular diffusion and volatilization under static quiescent conditions. The surface microlayer acted as a transient boundary between the water column and the atmosphere where the dynamic of TBT accumulation has the same trend as the dynamic of TBT ejection. This physical transfer mechanism might be of high significance in nearshore environments, harbors, and shallow channels where clouds of bubbles generated in the wake of large ships play an important role for the atmosphere/seawater chemical exchanges.  相似文献   

19.
The role of surfactant organic matter in marine aerosol production has been studied under conditions in which there is a large coverage of whitecaps on the sea surface. To improve the knowledge of matter exchange and pollutant recycling from the sea surface into the atmosphere, a spray drop adsorption model (SDAM) was developed and the validity of the proposed model verified by the following experimental results: (1) an increase of surfactant matter on the sea surface during rough sea conditions (‘surface wave concentration'); (2) an (hyperbolic-like) increase of the enrichment ratio (ER) of surfactant fluorescent organic matter (SFOM), made up predominantly by humic substances (HS), as the particle size decrease; (3) a similar behaviour for elements with pollutant properties, and which are known to interact with HS and other surfactant materials, considered pollution tracers. An additional laboratory experiment, based on the adsorption model conditions, gives enrichment ratio greater than unity for K and Ca. The first results on marine aerosols trapped in marine clouds (at 1000 m above sea level and at 100 km from the coast) seem to further support the proposed model and its ability to predict the transition from saline to almost entirely organic particles for the smaller fractions of marine aerosols. The possible contribution of these particles to the recycling and to the long range transport of pollutants via marine aerosols has been considered.  相似文献   

20.
The relationships existing between the protein-containing fraction of particulate matter and amino acids dissolved in seawater were studied in the Gulf of Marseille at different periods of the year. The concentration of particulate proteins was almost zero in February and attained maximum values during April and May, the average concentrations of dissolved amino acids (total) varied between 900 and 1200 nmole l?1 but larger variations were encountered at the surface and in the vicinity of the sediment. The influence of meteorological conditions and the effect of the sediment on the distribution of nitrogenous substances were taken into account. Combined dissolved amino acids were more abundant than free dissolved amino acids in 90% of the cases. The concentrations of dissolved amino acids observed in a zone bordering the North Mediterranean are comparable to those found in other regions of the world.  相似文献   

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