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1.
本研究选取5种海洋动植物大分子高聚物或其天然组织,包括虾壳、鱼鳞、海带叶片、几丁质和壳聚糖,分别在海水表层和沉积物环境中进行富集,定期取样,通过高通量测序分析菌群多样性。结果发现,不同有机物原位富集的细菌多样性存在较大的差异,而且同种底物在海水表层与沉积物中的降解菌菌群差异较大。从物种多样性看,在海水表层环境中富集的鱼鳞样品种群最丰富,而沉积物环境中富集的海带叶片样品菌群多样性最低,除其优势菌群为热袍菌门外,其他所有富集物中优势菌均为变形菌门。其中脱硫杆菌科、黄杆菌科、脱硫弧菌科和弧菌科占有较大比例,脱硫杆菌科在所有样品中优势较大,黄杆菌科在海水表层环境样品中为优势菌群,弧菌科在沉积物样品几丁质和壳聚糖样品中占比较高。本研究通过对同种海洋环境中不同富集样品之间以及同种底物不同环境中富集菌群之间的比较,分析结果得到了原位条件下参与大分子聚合物降解的菌群种类,但有待于在更多不同的海域富集物中进行验证。  相似文献   

2.
Experimental data on anoxic freshwater sediments from the Hamburg harbor indicate that commonly performed storage and pretreatment methods including aeration by drying strongly change the original associations of heavy metals with different sediment components. Oven-drying as well as freeze-drying under ‘vacuum’ affects metals originally bound to carbonate (Fe, Mn) and to the sulfidic/organic fraction (Zn, Cd, Cu, Pb), as indicated by sequential chemical extractions. While the easily oxidizable Cu and Pb portions are transferred mainly into the moderately reducible fraction, those of Zn and especially Cd are found in easily reducible and labile exchangeable fractions upon aeration of the sediment. Metals from only the latter fractions are potentially mobilizable via pore-water fluxes. Useful information on solid speciation influencing the mobility of contaminants in biogeochemically reactive sediments by the chemical leaching approach requires, therefore, proper and careful handling of the anoxic sediment samples.  相似文献   

3.
4.
生物降解甲壳质的研究   总被引:3,自引:0,他引:3  
介绍了利用生物 (主要是微生物 )降解甲壳质的一些研究进展 ,着重讨论了在甲壳质降解中起重要作用的几丁质酶的基本性质和分子生物学特征。指出了生物处理海洋资源 ,开发有用活性物质的应用前景。  相似文献   

5.
The speciation of dissolved iodine and the distributions of the iodine species in the deep Chesapeake Bay underwent seasonal variations in response to changes in the prevailing redox condition. In the deep water, the ratios of iodate to iodide and iodate to inorganic iodine decreased progressively from the Winter through the Summer as the deep water became more poorly oxygenated before they rebounded in the Fall when the deep water became re-oxygenated again. The composition of the surface water followed the same trend. However, in this case, the higher biological activities in the Spring and the Summer could also have enhanced the biologically mediated reduction of iodate to iodide by phytoplankton and contributed to the lower ratios found during those seasons. Superimposed on this redox cycle was a cycle of input and removal of dissolved iodine probably as a result of the interactions between the water column and the underlying sediments. Iodine was added to the Bay during the Summer when the deep water was more reducing and removed from the Bay in the Fall when the deep water became re-oxygenated. A third cycle was the inter-conversion between inorganic iodine and ‘dissolved organic iodine’, or ‘‘DOI’’. The conversion of inorganic iodine to ‘DOI’ was more prevalent in the Spring. As a result of these biogeochemical reactions in the Bay, during exchanges between the Bay and the North Atlantic, iodate-rich and ‘DOI’-poor water was imported into the Bay while iodide- and ‘DOI’-rich water was exported to the Atlantic. The export of iodide from these geochemically reactive systems along the land margins contributes to the enrichment of iodide in the surface open oceans.  相似文献   

6.
C. Arnosti   《Marine Chemistry》2004,92(1-4):263
The observation that a fraction of organic matter produced in marine systems evades the concerted efforts of microbial communities and is buried in sediments suggests that there are ‘speed bumps’ in carbon degradation pathways that impede microbially driven remineralization processes. The initial step in degradation of macromolecules, extracellular enzymatic hydrolysis, is often stated to be ‘the’ rate-limiting step in carbon remineralization. Experimental investigations described here, however, demonstrate that at least in certain cases, microbes produce extracellular enzymes on time scales of hours to tens of hours in response to substrate addition, and hydrolysis is extremely rapid. If enzymatic hydrolysis can be rapid, what factors slow or stop organic matter degradation? A lack of the correct inducer to initiate enzyme production, and/or a lack of the correct organism to produce the required enzyme, may result in a complete lack of hydrolysis in certain environments—a barricade, rather than a speed bump. Preliminary evidence supporting this hypothesis includes a comparison of polysaccharide hydrolysis in seawater and sediments, which demonstrates that the spectrum of enzymes active in seawater and sediments are fundamentally different. Furthermore, a survey of enzyme activities in surface waters from a range of locations suggests that pelagic microbial communities also differ widely in their abilities to express specific extracellular enzymes. Trans-membrane transport through porins is yet another potential location of structure-related selectivity.Our efforts to identify speed bumps and barricades are hampered by our inability to structurally characterize in sufficient detail the macromolecular structures present in marine systems. Furthermore, assessments of organic matter ‘quality’ from a chemical perspective do not necessarily accurately reflect the availability of organic carbon to microbial communities. For these communities, in fact, ‘quality’ may be a variable, which depends on the enzymatic and uptake capabilities of community members. To begin to assess substrate structure and quality from a microbial perspective, we will have to combine specific knowledge of macromolecular structures with detailed investigations of the enzymatic and transport capabilities of heterotrophic marine microbes.  相似文献   

7.
The effects of buried decaying macroalgae on meiobenthos were examined in intertidal sandy sediments of the Wadden Sea of Lower Saxony. In situ experiments confirmed that one of the principal causes of the formation of reduced surface sediments or ‘black spots’ on the tidal flats is the increasing occurrence and subsequent decomposition of filamentous green algae (Enteromorpha spp.) buried in the sediment. Five to fifteen days after algal material had been buried, the sediment surface turned black. The impact of these black spots on meiobenthos was dramatic: the changed chemical conditions in the sediment resulted in long and drastic reductions in meiofaunal abundance and number of taxa. A multi-dimensional scaling (MDS) analysis of data on meiobenthic abundances revealed that samples from black-spot areas were clearly separated from those of control and reference areas. Re-oxidized black spots showed recolonization by meiofaunal animals, with numbers of individuals and taxa similar to those of oxidized surface sediments. The use of abundances of members of higher meiobenthic taxa to monitor changes in the sediment's chemistry, especially those caused by biomass overload, is discussed.  相似文献   

8.
酶法制备几丁寡糖和壳糖研究现状与进展   总被引:15,自引:0,他引:15  
对用酶法制备几丁寡糖和壳寡糖研究现状与进展进行了综述。几丁质酶、壳聚糖酶、溶菌酶和 N-乙酰葡萄糖胺酶等专一性的水解酶及糖酶、蛋白酶、脂肪酶等水解酶对几丁质和壳聚糖都具有部分或完全非专一性水解作用。介绍了这些酶类的作用机理及相关微生物的种类和作用条件  相似文献   

9.
In order to gain a better understanding of biological and geochemical processes, sequential extraction techniques are widely employed to obtain information about the so-called ‘solid-speciation’ of chemical elements in soils and in suspended and deposited sediments. This present paper aims to review the different problems involved with such techniques and to specify the nature of their operation. Beyond the importance of sampling and pretreatment it is shown that the specificity and the reproducibility of the method greatly depends upon the chemical properties of the element and the chemical composition of the samples. Accordingly, these methods provide, at best, a gradient for the physicochemical association strength between trace elements and solid particles rather than their actual speciation. As previously underlined by W.F. Pickering (Crit. Rev. Anal. Chem., 2 (1981) 223–266) it is shown that, ‘a careless usage of these techniques without an appreciation of their pitfalls and limitations must lead to further generation of erroneous or misleading data’. Despite these inherent limitations, some useful information has been obtained in the fields of engineering and geoscience. However, the original idea which led to the development of the methods, i.e. the estimation of trace elements bioavailability, generally failed.  相似文献   

10.
A sequential leaching technique has been used to characterize the solid state speciation of total copper (∑Cu) among a number of operationally defined host fractions in surface seawater particulates from the Atlantic Ocean, a diagenetically active hemipelagic sediment core from the eastern Mediterranean, a turbidite - rich sediment core from the Madeira Abyssal Plain and a series of 79 Atlantic Ocean surface or near surface sediments. Around 50% of the ∑Cu in the surface water particulates is held in organic associations. When the material is deposited at the sediment surface, following its entry into the down-column carbon flux, the ∑Cu undergoes phase transformations as the organic carriers are destroyed. However, some of the organically associated copper (Cu5) is preserved in the sediments, the amount depending on the diagenetic environment of deposition. The relationship between ∑Cu and organic carbon in an oceanic sediment may be masked, but the partitioning speciation data has shown that good correlations can be found between organic carbon and Cu5. The concentration of Cu5 in Atlantic Ocean surface sediments is highest in hemipelagic (diagenetically active) sediments deposited in the marginal regions, and lowest in open-ocean (less diagenetically active) sediments of the Mid-Atlantic Ridge and ridge flanks. The marginal sediments contain an average of 20% of their total Cu in an organic association, with the result that these sediments can act as traps for seawater-derived Cu that would normally be regarded as being ‘reactive’ in the marine environment. To a first approximation, the preservation of Cu5 in the sediments mimics that of primary production in the overlying waters, and so ‘fingerprints’ the operation of the global ocean carbon flux in oceanic deposits. However, the relationship can be perturbed by the off-shelf transport of organic-rich, Cu5-containing, turbidites which can result in the transfer and burial of organic copper host fractions in open-ocean oxic environments.  相似文献   

11.
Coastal marine sediment, air and seawater samples were collected at six sampling stations in the Eastern Mediterranean Sea distant from pollutant point sources. All sediment samples were analyzed to determine polycyclic aromatic hydrocarbon (PAH), black carbon (BC) and organic carbon (OC) contents. The PAH contents of gaseous and seawater samples of the study were determined in order to evaluate the role of air–sea exchange as PAH nonpoint source to the marine sediments. The average concentration of the total PAHs (∑PAHs) in the sediments varied from 2.2 to 1056.2 ng g−1 dry weight. The average BC and OC contents varied from 0.3 to 5.6 and from 2.9 to 21.4 mg g−1 dry weight, respectively. ∑PAH concentration in the marine atmosphere varied from 20.0 to 83.2 ng m−3. Air–water exchange flux (FA–W) estimation has indicated air transport as a significant source of PAHs to pristine marine sediments of Eastern Mediterranean. In addition, the significant correlation between the PAHs and the organic and soot carbon content further suggests the importance of atmospheric input of PAHs to the sediments.  相似文献   

12.
Suspended particle dynamics were investigated in the Ogeechee River Estuary during neap tide in July 1996. Samples were operationally separated into ‘ truly suspended ’ (settling velocity <0·006 cm s−1) and ‘ settleable ’ (settling velocity >0·006 cm s−1) fractions over the course of a tidal cycle to determine whether these two fractions were comprised of particles with differing biological and chemical characteristics. Total suspended sediment, organic carbon and nitrogen, chlorophyll a and phaeopigment concentrations were measured in each fraction, as well as rates of bacterial hydrolytic enzyme activity [β-1,4-glucosidase (βGase) and β-xylosidase (βXase)]. The majority of the suspended sediment (by weight) was in the truly suspended fraction; all measured parameters were largely associated with this fraction as well. When compared to the settleable material, the truly suspended material was significantly higher in % POC (5·7±0·6 vs. 3·9±1·8), % chlorophyll (0·07±0·02 vs. 0·03±0·01), % phaeopigment (0·030±0·006 vs. 0·018±0·012), and weight-specific maximal uptake rates (Vmaxper mg suspended sediment) of both enzymes (1·8±0·4 vs. 0·7± 0·2 nmol mg−1 h−1βGase and 1·1±0·3vs . 0·3±0·2 nmol mg−1 h−1βXase), providing clear evidence for a qualitative distinction between the two fractions. These results are interpreted to mean that the more organic-rich, biologically active material associated with the suspended fraction is likely to have a different fate in this Estuary, as ‘ truly suspended ’ sediments will be readily transported whereas ‘ settleable ’ sediments will settle and be resuspended with each tide. These types of qualitative differences should be incorporated into models of particle dynamics in estuaries.  相似文献   

13.
Major sequence boundaries associated with eustatic sea level changes are correlated to the general stratigraphy of the north-eastern Gulf of Mexico. The details of a Middle Cretaceous Flooding Surface, marking a major break in sedimentation, are documented. The sequence stratigraphic work provides an example of the ‘stratigraphic signature of the Neogene’. Three major episodes of sediment accumulation are represented by: (1) Late Jurassic (150.5 Ma) to Middle Cretaceous (94 Ma) aggradation and progradation of sediments with significant sediment accumulation in the present shelf and slope areas; (2) an extended period of starved sedimentation during 94-30 Ma corresponding to Middle Cretaceous flooding events (93.5 and 91.5 Ma) and the lack of sediment supply; and (3) since Late Oligocene time, unusually rapid sedimentation rates that characterize the deep water study area. These patterns of sediment accumulation directly affect the formation of allochthonous salt in the study area.  相似文献   

14.
The sediments of Southampton Water were analysed for petroleum hydrocarbons to determine the fate of petrochemical refinery waste in the estuary. Much of the petroleum hydrocarbons appears to be removed by adsorption onto estuarine sediments close to source. Surface sediment concentrations range from 3·1mg/g dry weight near a refinery to 0·5 mg/g dry weight at locations distant from the refinery.The absence of any change with depth in total hydrocarbon concentrations from some sediment cores and the presence of distinct ‘oil’ horizons in others suggests that mixing of sediments in the area is very random. Sedimentation rates in areas where a distinct oil horizon was observed ranged from 1 to 3cm a year.  相似文献   

15.
We have analyzed 33 Pliocene bulk sediment samples from Ocean Drilling Program Site 1085 in the Cape Basin, located offshore of western Africa in the Angola–Benguela Current system, for 17 major and trace elements, and interpreted their associations and temporal variations in the context of an allied data set of CaCO3, opal, and Corg. We base our interpretations on elemental ratios, accumulation rates, inter-element correlations, and several multi-element statistical techniques. On the basis of qualitative assessment of downhole changes in the distributions of P and Ba, utilized as proxies of export production, we conclude that highs in bulk and biogenic accumulation that occur at 3.2 Ma, 3.0 Ma, 2.4 Ma, and 2.25 Ma were caused by increases in export production as well as terrigenous flux, and record a greater sequestering of organic matter during these time periods. Studies of refractory elements and other indicator proxies (SiO2, Al2O3, TiO2, Fe2O3, MgO, V, Cr, Sr, and Zr) strongly suggest that the terrigenous component of the bulk sediment is composed of two compositional end-members, one being ‘basaltic’ in composition and the other similar to an ‘average shale’. The basaltic end-member comprises approximately 10–15% of the total bulk sediment and its presence is consistent with the local geology of source material in the drainage basin of the nearby Orange River. The increase in bulk accumulation at 2.4 Ma appears to reflect a greater relative increase in basaltic input than the relative increase in shale-type input. Although studies such as this cannot precisely identify the transport mechanisms of the different terrigenous components, these results are most consistent with variations in sea level (and associated changes in shelf geometry and fluvial input) being responsible for the changing depositional conditions along the Angolan Margin during this time period.  相似文献   

16.
甲壳质生产物料平衡分析及清洁生产途径   总被引:2,自引:0,他引:2  
简要介绍了甲壳质传统酸碱法、酸碱法和微生物法清洁生产工艺及其优缺点以及主要物料投入和流失物,分析了以废弃虾、蟹壳为原料,以酸碱法作试剂生产甲壳质的污染状况;通过对酸碱法清洁生产工艺与传统生产工艺的比较,提出了酸碱法生产中使甲壳质废水排放达标的若干对策,指出了甲壳质清洁生产的可行途径;同时展望了微生物法清洁生产甲壳质的前景。  相似文献   

17.
Multidimensional statistical analysis was used to study the polychaete distribution in soft-bottoms of two coastal areas of the Tyrrhenian Sea (Italy), which are influenced by the discharges of the rivers Tiber and Ombrone. In both areas the distributional patterns of these organisms are determined mainly by sediment types and related factors such as hydrodynamics, river input, and sedimentation. The grain-size gradient from the coast to the open sea affects not only species composition, but also species richness, diversity and abundance.In both areas three main communities have been identified: a sandy biocoenosis, a mixed-sediment biocoenosis and a muddy biocoenosis. The sandy coastal community is characterized by only a few species, while the intermediate zone of sandy-mud sediments presents the highest species richness and diversity. At the mouth of the River Tiber the influence of the river is more evident than at the mouth of the River Ombrone. This is due to the Tiber's greater river flow, which determines an environmental uniformity and a ‘cenotic continuum’ from sandy to muddy communities. This does not occur at the mouth of the Ombrone, where the river flow is less important and the polychaete communities are better defined.  相似文献   

18.
The performance of extractants commonly used in the determination of acid volatile sulfide minerals (e.g., ‘amorphous-FeS’, mackinawite and greigite) and pyrite has been evaluated using pure mineral phases and anoxic sediments. ‘Amorphous-FeS’ and mackinawite are quantitatively recovered by most cold acid extractions, but greigite recovery is incomplete. Harsher extractants with reducing agents are necessary for the complete recovery of greigite, but dissolution of fine-grained synthetic pyrite occurs under such conditions. A quantitative separation between greigite and pyrite is not possible using these techniques, but the use of ‘acid volatile sulfide’ and ‘pyrite’ as operational categories is adequate for most field studies.  相似文献   

19.
Metalliferous and pelagic sediments are exposed within and above the extrusive successions of the Upper Cretaceous Oman ophiolite which, on the basis of mostly geochemical evidence, is believed to have formed in an incipient marginal basin setting located above a NE-dipping subduction zone. The ophiolitic extrusives document various volcano-tectonic settings which include the axial zones of a spreading ridge, fault-controlled seamounts and off-axis volcanic edifices. Most of the Fe, Mn and trace metal-enriched sediments studied are interpreted as precipitates formed by oxidation of solutions derived from high-temperature sulphide-precipitating vents. The trace element content (e.g. REE and Sr) was largely scavenged from seawater. The sediments are similar to the dispersed metalliferous sediments on the flanks of modern spreading ridges, and the ‘basal’ sediments of DSDP wells and of other ophiolite complexes (e.g. Troodos, Cyprus).Distinctive mound structures located low in the lavas are attributed to percolation of sulphide-rich solutions into already deposited metalliferous oxide sediments. The resulting iron-silica rock was probably originally precipitated as ferruginous silicates.Major massive sulphides formed off-axis at the base of intermediate-basic edifices of volcanic arc affinities. Fe, Mn and trace metal enrichment in the sediment cover of a flat-topped seamount of axial lavas is interpreted as a dispersion halo around the largest massive sulphide orebody which is situated 5 km away (Lasail). Small massive sulphide bodies are common in the axial lavas particularly along major seafloor fault zones. The metalliferous sediments, locally precipitated near these vents, are ferromanganiferous, but trace metal-depleted.The metalliferous and pelagic sediment cover of the extrusive successions, generally, documents waning hydrothermal input after volcanism ended in the area.A model is discussed in which the ophiolite was created at a spreading axis above a subduction zone dipping away from the Arabian continental margin. With progressive subduction this crust approached the margin. Initially, calcareous sediment accumulated above the calcite compensation depth (CCD), but then non-calcareous radiolarites were deposited as the ophiolitic crust approached the continental margin where the CCD was higher and marginal upwelling possibly enhanced productivity. As the edge of the Arabian continental margin entered the trench, the over-riding ophiolite was regionally uplifted allowing short-lived chalk accumulation above the CCD. This was followed by volcaniclastic deposition related to the tectonic emplacement.  相似文献   

20.
Summer porewater and spring and summer surficial sediment samples were collected from 26 locations in the intertidal region of the Fraser River estuary. Porewaters were analysed for dissolved iron and manganese (as defined by species <0·2μm in diameter) to assess the contribution of diagenesis to concentrations of iron and manganese oxides at the sediment–water interface. Surficial sediment samples were geochemically characterized as: % organic matter (% LOI); reducible iron (RED Fe, iron oxides) and easily reducible manganese (ER Mn, manganese oxides). Grain size at each site was also determined. The sediment geochemical matrix, as defined by the above four parameters, was highly heterogeneous throughout the intertidal region (three-way ANOVA;P<0·0001). For RED Fe and ER Mn, this heterogeneity could be explained by either diagenetic processes (RED Fe) or by a combination of the proximity of the sample sites to the mouth of the Fraser River estuary plus diagenetic processes (ER Mn). Correlation (Spearman Rank Correlation Test (rs), of dissolved iron within the subsurface sediments with amounts of RED Fe recovered from the associated surface sediments was highly significant (rs=0·80, P<0·0001); high concentrations of RED Fe at the sediment–water interface co-occurred with high concentrations of dissolved iron, regardless of the proximity of the sample locations to riverine input. Compared with iron, the relationship between dissolved manganese and ER Mn from surface sediments was lower (rs=0·58;P<0·0008). Locations most strongly influenced by the Fraser River contained greater concentrations of ER Mn at the sediment–water interface than that which would be expected based on the contribution from diagenesis alone. Sediment grain size and organic matter were also influenced by the proximity to riverine input. Surficial sediment of sites close to the river mouth were comprised primarily of percent silt (2·0μm–50μm) whereas sites not influenced by riverine input were primarily percent sand (grain size >50μm). Concentrations of organic matter declined from the mouth to the foreslope of the estuary. With the exception of RED Fe, temporal variation (May vs July) was insignificant (P>0·05, three-way ANOVA). Concentrations of RED Fe recovered from the surficial sediments were in general greater in the summer vs spring months, although spring and summer values were highly correlated (Pearson Product Moment Correlation Coefficient; PPCC; R=0·89;P<0·0001). As the bioavailability of metals is dependent on sediment geochemistry, availability throughout the intertidal region will also be spatially dependent. This heterogeneity needs to be taken into account in studies addressing the impact of metals on estuarine systems.  相似文献   

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