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1.
An evaluation of the distribution of P concentrations in streamflow, P fractions andthe microbial biomass P pool was made of bed and bank sediments along a lowlandstream in New Zealand. Agricultural intensification increased downstream. However,most P fractions decreased downstream (total P decreased from c. 400 to 250 mg kg-1) in bed sediments, while P in streamflow remained relatively constant (generally < 0.005 mg l-1) and sediment microbial P increased from 2 to 8 mg kg-1. An investigation of P release from dried and rewetted sediments showed that solution P (CaCl2-P) increased, on average > 300%, and proportional to the size of the microbial biomass P pool before drying, except in sediments with much organic carbon (OC). When supplied with a P source (1 mg l-1) and then simultaneously with a C source (glucose, 100 mg l-1), all sediment behaved similarly and biotic sorption accounted for, on average, 27 and 34% of the total sediment uptake, respectively (maximum of 58%). The quantity of P taken up was related to the initial size of the microbial biomass P pool, and the availability of P as influenced by organic P complexes and OC. The sediment microbial biomass represents a transient, but small store of P could be useful to indicate bioavailable P inputs.  相似文献   

2.
《Applied Geochemistry》2003,18(7):955-972
This review highlights the major progress over the last decade on characterization of geochemically heterogeneous soil/sediment organic matter (SOM) and the impacts of SOM heterogeneity on sorption and desorption of hydrophobic organic contaminants (HOCs) under equilibrium and rate limiting conditions. Sorption and desorption by soils and sediments are fundamental processes controlling fate and transport of less polar and nonpolar organic pollutants in surface aquatic and groundwater systems. Recent studies have shown that soils and sediments exhibit an array of HOC sorption phenomena that are inconsistent with an early partition model based on an assumption of homogeneous gel-like SOM. Increasing data have revealed that isotherm nonlinearity, varied sorption capacity, sorption–desorption hysteresis, and slow rates of sorption and desorption are characteristics for HOC sorption by soils and sediments. These phenomena have been shown to result from different types of condensed SOM that exhibit capacity limiting sorption processes. Recent findings of glass transition phenomena and the nonlinear HOC sorption by humic acids provide a scientific foundation for drawing an analogy between humic acids and synthetic organic polymers that supports a dual mode model for sorption by soils and sediments. Humic acid is glassy or rigid at temperatures lower than its glass transition temperature and exhibits relatively nonlinear sorption isotherms for HOCs. Fractionation and quantification of SOM indicate that soils and sediments contain significant amounts of black carbon and kerogen of different origins. These particulate organic materials have rigid 3-dimensional structures and are often less polar compared to humic substances. Limited studies show that black carbon and kerogen exhibit nonlinear sorption for HOCs and may dominate the overall nonlinear sorption by soils and sediments.  相似文献   

3.
Black carbon (BC), especially biochar, is a potential material for the remediation of hydrophobic organic compounds (HOCs) pollution in soils and sediments. Recent studies have reported that the adsorption capability of BC in sediment was reduced as time increased. It was hypothesised that this behaviour was caused by the presence of natural organic matter (NOM), but few systematic studies have examined the influence of NOM on the sorption ability of BC in sediment (S). The results of this study revealed that a humic acid (HA) coating changed the surface properties, blocked the micropores, and decreased the sorption capacity of rice-straw biochar (RBC) towards pentachlorophenol. With increasing aging time, the reductions in the sorption capacity of the S + RBC and S + HA + RBC systems occurred more rapidly than in the S + HA/RBC (HA-coated RBC) system, and the sorption curves became closer to that of the S + HA/RBC system, indicating that HA may play a primary role in reducing the sorption capacity of RBC in the sediment. With higher HA contents, the sorption capacity of the complex sediments was lower and decreased more rapidly.  相似文献   

4.
Burrowing crabs (Chasmagnathus granulata), sediment collected from inside and outside crab burrows as well as outside the crab bed, and cordgrass (Spartina densiflora) were collected from intertidal mudflat and cordgrass marsh habitats and analyzed for concentrations of polychlorinated biphenyl (PCB) congeners and organochlorine (OC) compounds to test the hypothesis that there are differences in the distribution and bioaccumulation of OC contaminants in coastal lagoon habitats in Argentina. PCB concentrations were relatively low, although the penta- and hexachlorobiphenyl detected in sediments and biota indicated that there had been direct inputs of PCBs into the ecosystem. Heptachlor epoxide, dieldrin, endosulfan sulphate, chlordane compounds, DDT and metabolites, and hexachlorocyclohexanes (HCHs) were the major pesticides detected in sediment and biota samples. When lipid-normalized concentration data for all OC pesticides in crabs were summed together (ΣOCC), there were higher concentrations in crabs from the cordgrass habitat in comparison to crabs from the mudflat. In sediment samples, there were no significant differences in percent organic matter of marsh and mudflat sediments, but the concentrations of ΣOCC normalized to organic carbon were higher in the sediments collected in the cordgrass marsh. Samples of rhizomes and roots from the cordgrass contained high concentrations of OC compounds and it was estimated that 2.4 kg of heptachlor epoxide, the most abundant OC pesticide, may be present in the total cordgrass root biomass in Mar Chiquita lagoon. These data indicated that the cordgrass in coastal lagoon environments is an important factor in determining the distribution of persistent contaminants, and that a significant portion of the total burden of these hydrophobic compounds may be deposited in cordgrass biomass.  相似文献   

5.
《Organic Geochemistry》1999,30(8):929-936
The sorption isotherms of benzene, naphthalene, fluorene and phenanthrene for a suite of whole and lipid-extracted soils are presented. The sorption of benzene to two different peats displays linear characteristics which are consistent with the partitioning model of sorption. The sorption of the PAHs to three different mineral soils show marked nonlinear character. The nonlinear sorptive character of the soil organic matter can be described by site specific sorption occurring within the soil organic matrix. Removal of the lipids via Soxhlet extraction increases the nonlinear character of the sorption isotherms as well as doubles the sorptive capacity of the mineral soils for the PAHs studied. This indicates that the lipids naturally present in the soil strongly compete for hydrophobic sorption sites present in the soil organic matter matrix.  相似文献   

6.
The effect of organic matter on the sorption of dissolved organic matter (DOM) on lake sediments is critical to understanding the fate and transport of contaminants at the sediment–water interface in lake ecosystems. Results indicate that DOM sorption on sediment is largely due to ligand exchange between the DOM and hydroxyl groups, and the amount of DOC sorbed is a linear function of added DOC. With increasing organic matter content the sediment has lower binding strength, higher releasing ability for DOM, and the higher amount of DOM sorbed by sediment naturally. There was no clear difference before and after the sediment was treated with H2O2, but the constant b implied that after the sediments were treated DOC release was promoted. Organic matter in the sediment tends to impede the sorption of DOC and results in a remarkable decrease in DOC sorption rates.  相似文献   

7.
Surface soil and sediment samples collected along a forest-brackish marsh-salt marsh transect in a southeastern U.S. estuary were separated into three different fractions (sand, macro-organic matter, and humus) based on size and density. Elemental, stable carbon isotope, and lignin analyses of these samples reveal important contrasts in the quantity, composition, and sources of organic matter, between forest and marsh sites. Elevated nitrogen contents in humus samples suggest nitrogen incorporation during humification is most extensive in forest soils relative to the marsh sites. The lignin compositions of the macro-organic and humus samples reflect the predominant type of vegetation at each site. Lignin phenol ratios indicate that woody and nonwoody litter from, gymnosperm and angiosperms trees (pines and oaks) is the major source of vascular plant-derived organic matter in the forest site and that angiosperm, grasses (Juncus andSpartina) are the major sources of lignin at the marsh sites. The phenol distributions also reveal that oxidative degradation of lignin is most extensive in the forest and brackish marsh zones whereas little lignin decay occurs in the salt marsh samples. In forest soils, most organic matter originates from highly altered forest vegetation while at the brackish marsh site organic matter is a mixture of degradedJuncus materials and microbial/algal remains. Organic matter in the salt marsh appears to be composed of a more complex mixture of sources, including degradedSpartina detritus as well as algal and microbial inputs. Microbial methane oxidation appears to be an important process and a source of13C depleted organic carbon in subsurface sediments at this site.  相似文献   

8.
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9.
Analyses of organic carbon, total nitrogen, and inorganically bound ammonium (exchangeable and fixed ammonium) in two oxic deep-sea sediment cores from the Central Pacific Ocean revealed insufficiently high inorganic ammonium contents of these sediments to explain the low C/N ratios, although representing 20–45% of the total nitrogen.Both, organic carbon/total nitrogen ratios (ranging from 3.9?1.3) and organic carbon/organic nitrogen ratios (5.6?1.9) decrease with increasing sediment depth, the latter indicating a real enrichment of organic nitrogen compounds during diagenesis relative to total organic matter.Organic matter/alumina relationships indicate that this unusual preservation of organic nitrogen compounds is probably caused by sorption to clay minerals protecting them against bacterial attack.  相似文献   

10.
红壤中矿物表面对腐殖质吸附萘的影响   总被引：5，自引：1，他引：5  
矿物表面可改变土壤腐殖质对疏水性有机污染物的结合能力。采用红壤和高岭石分别与胡敏酸结合制备得到的两种复合体对萘的吸附等温线非线性显著,其n=0.76或0.74,并且有机碳归一化吸附分配系数的实验值Koacds是采用Kow计算得出的理论值Koc的5倍以上,表明红壤、高岭石均对腐殖质吸附萘有强化作用,且红壤较之高岭石对腐殖质吸附萘的影响稍强些。主要原因是,红壤中除了高岭石外,还有与腐殖质结合力很强的铁氧化物,而且很可能是吸附态腐殖质组成结构形态发生了有利于对萘吸附的改变。  相似文献   

11.
The importance of intertidal estuarine habitats, like salt marsh and oyster reef, has been well established, as has their ubiquitous loss along our coasts with resultant forfeiture of the ecosystem services they provide. Furthering our understanding of how these habitats are evolving in the face of anthropogenic and climate driven changes will help improve management strategies. Previous work has shown that the growth and productivity of both oyster reefs and salt marshes are strongly linked to elevation in the intertidal zone (duration of aerial exposure). We build on that research by examining the growth of marsh-fringing oyster reefs at yearly to decadal time scales and examine movement of the boundary between oyster reef and salt marsh at decadal to centennial time scales. We show that the growth of marsh-fringing reefs is strongly associated to the duration of aerial exposure, with little growth occurring below mean low water and above mean sea level. Marsh-shoreline movement, in the presence or absence of fringing oyster reefs, was reconstructed using transects of sediment cores. Carbonaceous marsh sediments sampled below the modern fringing oyster reefs indicate that marsh shorelines within Back Sound, North Carolina are predominantly in a state of transgression (landward retreat), and modern oyster-reef locations were previously occupied by salt marsh within the past two centuries. Cores fronting transgressive marsh shorelines absent fringing reefs sampled thinner and less extensive carbonaceous marsh sediment than at sites with fringing reefs. This indicates that fringing reefs are preserving carbonaceous marsh sediment from total erosion as they transgress and colonize the exposed marsh shoreline making marsh sediments more resistant to erosion. The amount of marsh sediment preservation underneath the reef scales with the reef’s relief, as reefs with the greatest relief were level with the marsh platform, preserving a maximum amount of carbonaceous sediments during transgression by buffering the marsh from erosional processes. Thus, fringing oyster reefs not only have the capacity to shelter shorelines but, if located at the ideal tidal elevation, they also keep up with accelerating sea-level rise and cap carbonaceous sediments, protecting them from erosion, as reefs develop along the marsh.  相似文献   

12.
To understand the behavior of trace metals in the salt marsh at Skallingen, Danish Wadden Sea, we investigated a profile from surface to 25?cm depth of the salt marsh sediment, focusing primarily on clay mineralogy and grain size distribution of the sediments and their relationship with trace metals. The clay assembly of the sediment consists of illite, kaolinite and much less chlorite and smectite. The major clay minerals of illite, kaolinite as well as chlorite correlate very poorly with all the trace metals investigated, due probably to the weak competing strength of these clays compared with the other adsorbents and to low availability of the mobile trace metals in the system. Correlation between trace metals and clay minerals may therefore be used as an indicator in environmental assessment. Fine grain fractions of the sediment increased markedly after salt marsh invasion in about 1931 but decreased after 1964. This increase was contributed mainly by the grains finer than 20???m while the fraction of 40?C63???m actually decreased soon after the invasion. The relation between most of the trace metals and grain size distributions is close in general but far from linear. The drastic turning point is observed at about 30???m, around where the correlation coefficient r drops from 0.8 to 0.1. Adsorption is the controlling mechanism for the behavior of trace metals in the salt marsh. Fe/Mn (hydr)oxides and organic matter play the key role.  相似文献   

13.
A process-based numerical model is applied to investigate sediment transport dynamics and sediment budget in tide-dominated estuaries under different salt marsh erosion scenarios. Using a typical funnel-shaped estuary (Ribble Estuary, UK) as a study site, it is found that the remobilization of sediments within the estuary is increased as a result of the tidal inundation of the eroded salt marsh. The landward export of the finest sediment is also intensified. The relationship between salt marsh erosion and net landward export of sediments has been found to be non-linear—with the first 30% salt marsh erosion causing most of the predicted export. The presence of vegetation also influences the sediment budget. Results suggest that vegetation reduces the amount of sediment being transported upstream. Again, the trapping effect of salt marsh in terms of plant density is non-linear. Whilst a vegetated surface with a stem density of 64 plants/m2 decreased the net landward export of very fine sand by around 50%, a further increase in stem density from 64 to 512 plants/m2 had a relatively small effect.  相似文献   

14.
Vertical accretion of impounded marsh and adjacent natural marsh at four sites in southwestern Louisiana was estimated in 1994 by determining the depth of a stratum containing137Cs deposited in 1963. With relative marsh elevation, soil bulk density, organic matter content, and organic and mineral matter accumulation rates were used to describe soil formation. Three sites were impounded in 1956 and one site in 1951. Impounded marshes had lower marsh surface elevation than natural marshes because of hydrologic isolation from tidal sediment subsidies and substrate oxidation during forced drying. The elevation of natural marshes ranged from 12 cm to 42 cm higher than the elevation of the impounded marshes in 1963 and from 20 cm to 32 cm higher in 1994. Vertical accretion between 1963 and 1994 ranged from 9 cm to 28 cm in impounded marsh and from 15 cm to 21.5 cm in natural marsh. Only in impounded marsh that remained permanently flooded was accretion greater than in natural marsh.  相似文献   

15.
沉水植物黑藻对沉积物磷吸附动力学的影响   总被引：4，自引：0，他引：4  
在室内模拟条件下,通过吸附动力学实验,研究了沉水植物黑藻对沉积物吸附磷动力学模型拟合和吸附速度的影响,并从有机质和铁铝氧化物含量的角度,讨论了沉水植物黑藻对沉积物吸附磷动力学的影响机理。初步得出如下结论:(1)一级反应动力学模型虽然从模型拟合的角度达到了极显著水平,但不能真实地反映沉水植物对沉积物吸附磷动力学过程的影响。其余三个模型均能很好地反映,其中抛物线扩散模型的拟合效果最好,修正的Elovich模型和双常数速率模型的拟合效果较好。种植沉水植物与否并不影响这一趋势;(2)沉水植物黑藻提高了沉积物吸附磷的强度和速度,特别是提高了0～0.5h内的吸附速度,沉水植物影响有机质和铁铝氧化物含量是增强沉积物吸附磷强度和速度的重要机理。  相似文献   

16.
Many salt marshes in densely populated areas have been subjected to a reduction in tidal flow. In order to assess the impact of tidal flow restriction on marsh sedimentation processes, sediment cores were collected from flow-restricted restricted salt marshes along the Connecticut coast of Long Island Sound. Cores were also collected from unrestricted reference marshes and from a marsh that had been previously restricted but was restored to fuller tidal flushing in the 1970's. High bulk densities and low C and N concentrations were found at depth in the restricted marsh cores, which we attribute to a period of organic matter oxidation, sediment compaction, and marsh surface subsidence upon installation of flow restrictions (between 100 and 200 years before the present, depending on the marsh). Recent sedimentation rates at the restricted marshes (as determined by137Cs and210Pb dating) were positive and averaged 78% (137Cs) and 50% (210Pb) of reference marsh sedimentation rates. The accumulation of inorganic sediment was similar at the restricted and reference marshes, perhaps because of the seasonal operation of the tide gates, while organic sediment accretion (and pore space) was significantly lower in the restricted marshes, perhaps because of higher decomposition rates. Sedimentation rates at the restored marsh were significantly higher than at the reference marshes. This marsh has responded to the higher water levels resulting from restoration by a rapid increase in marsh surface elevation.  相似文献   

17.
Temporal and spatial variation in intertidal sedimentation rates   总被引：2，自引：0，他引：2  
Sediment deposition and erosion rates are reported for an intertidal zone in the Burry Inlet, South Wales. Measured deposition rates over the salt marsh are compared with deposition rates calculated from observed suspended sediment concentrations. Notably, it is concluded that residual turbulence at slack water should not be discounted when calculating deposition rates. Grain-size distributions of suspended sediments over the marsh surface, during flood and ebb tides, contrast with the grain-size distribution of deposited marsh sediments, the latter being significantly coarser. These data in conjunction with mass budget calculations are used to relate total annual deposition and sediment supply by tidal action during settled meteorological periods. The analysis suggests that episodic storm-induced sediment transport is probably an important mechanism for introducing coarse sediment on to the marsh surface. Finally, it is noted that seasonal reworking of the sandy non-cohesive sediments may be related to variations in the intensity of wave-breaking throughout the year.  相似文献   

18.
While cyanide is known to be produced by many organisms, including plants, bacteria, algae, fungi and some animals, it is generally thought that high levels of cyanide in aquatic systems require anthropogenic sources. Here, we report accumulation of relatively high levels of cyanide in non-polluted salt marsh sediments (up to 230 μmol kg?1). Concentrations of free cyanide up to 1.92 μmol L?1, which are toxic to aquatic life, were detected in the pore-waters. Concentration of total (free and complexed) cyanide in the pore-waters was up to 6.94 μmol L?1. Free cyanide, which is released to the marsh sediments, is attributed to processes associated with decomposition of cord grass, Spartina alterniflora, roots and possibly from other sources. This cyanide is rapidly complexed with iron and adsorbed on sedimentary organic matter. The ultimate cyanide sink is, however, associated with formation of thiocyanate by reaction with products of sulfide oxidation by Fe(III) minerals, especially polysulfides. The formation of thiocyanate by this pathway detoxifies two poisonous compounds, polysulfides and hydrogen cyanide, preventing release of free hydrogen cyanide from salt marsh sediments into overlying water or air.  相似文献   

19.
The pore waters of sediments from a salt marsh along the Delaware estuary have been analyzed for sulfur species and associated trace metals. Since the sediment interface is usually in contact with the atmosphere, the sulfur species are dependent on the production of hydrogen sulfide by sulfate reduction and subsequent oxidation by diffusing oxygen. The most important species observed are hydrogen sulfide, polysulfide ions and thiosulfate. Secondary reactions of hydrogen sulfide and polysulfides with decomposing organic matter yield significant concentrations of both thiols and organic polysulfides. Upon isolation of the sediment from the atmosphere due to tidal inundation, bacterial sulfate reduction becomes the dominant process. This results in the reduction of the polysulfides in agreement with thermodynamic predictions, and suggests that the redox couple sulfide/polysulfide is a good redox indicator under such reducing environments.The concentrations of trace elements Cu and Fe in the pore waters are mainly controlled by sulfide formation. Calculations show that copper is strongly complexed probably with organo-sulfur ligands. Iron might be complexed as such sulfur species to a much lesser extent than copper.  相似文献   

20.
Aliphatic hydrocarbon compositions were quantitatively characterized in plankton, sediment trap-collected particulate materials and sediments from Dabob Bay using high resolution glass capillary gas chromatography. The average net accumulation of individual hydrocarbons measured in a 1-yr series of sediment traps was compared with the net accumulation of corresponding compounds measured in three depth intervals of 210Pb-dated bottom sediments. Systematic and rapid decreases in the net accumulation of individual hydrocarbons were observed from the sediment traps to the sediments. Most pronounced decreases were measured for planktonically derived hydrocarbon constituents (e.g. pristane and two unsaturated compounds) which are rapidly remineralized at or near the sediment-water interface. Consequently, the amount of each compound measured in deposited sediments is not necessarily a quantitative indication of its initial flux to the sediments. The n-alkanes (C25,27,29,31). characteristic of terrestrial plant waxes, are the predominant hydrocarbons measured by 4–6 cm depth in these sediments and show reasonably constant net accumulation below this interval.Significant diagenetic alteration of the bulk organic matter contained in the average sediment trap particulate material is also noted through comparison with bottom sediments on the basis of organic C/N and δ13C measurements. Organic matter elementally similar to marine plankton is preferentially remineralized upon deposition of the sedimentary particulates. The residual organic matter remaining and buried in the bottom sediments closely resembles terrestrial organic matter.  相似文献   

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