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  • 1
    Electronic Resource
    Electronic Resource
    An analysis of the characteristics of rough bed turbulent shear stresses in an open channel (1997)
    Springer
    Stochastic environmental research and risk assessment 11 (1997), S. 193-210 
    Details
    ISSN: 1436-3259
    Keywords: Turbulence ; sediment ; fluvial ; river ; bursting process ; statistics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Architecture, Civil Engineering, Surveying , Energy, Environment Protection, Nuclear Power Engineering , Geography , Geosciences
    Notes: Abstract Entrainment of sediment particles from channel beds into the channel flow is influenced by the characteristics of the flow turbulence which produces stochastic shear stress fluctuations at the bed. Recent studies of the structure of turbulent flow has recognized the importance of bursting processes as important mechanisms for the transfer of momentum into the laminar boundary layer. Of these processes, the sweep event has been recognized as the most important bursting event for entrainment of sediment particles as it imposes forces in the direction of the flow resulting in movement of particles by rolling, sliding and occasionally saltating. Similarly, the ejection event has been recognized as important for sediment transport since these events maintain the sediment particles in suspension. In this study, the characteristics of bursting processes and, in particular, the sweep event were investigated in a flume with a rough bed. The instantaneous velocity fluctuations of the flow were measured in two-dimensions using a small electromagnetic velocity meter and the turbulent shear stresses were determined from these velocity fluctuations. It was found that the shear stress applied to the sediment particles on the bed resulting from sweep events depends on the magnitude of the turbulent shear stress and its probability distribution. A statistical analysis of the experimental data was undertaken and it was found necessary to apply a Box-Cox transformation to transform the data into a normally distributed sample. This enabled determination of the mean shear stress, angle of action and standard error of estimate for sweep and ejection events. These instantaneous shear stresses were found to be greater than the mean flow shear stress and for the sweep event to be approximately 40 percent greater near the channel bed. Results from this analysis suggest that the critical shear stress determined from Shield's diagram is not sufficient to predict the initiation of motion due to its use of the temporal mean shear stress. It is suggested that initiation of particle motion, but not continuous motion, can occur earlier than suggested by Shield's diagram due to the higher shear stresses imposed on the particles by the stochastic shear stresses resulting from turbulence within the flow.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02427915
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  • 2
    Electronic Resource
    Electronic Resource
    The selectivity of a sequential extraction procedure for the determination of iron oxyhydroxides andiron sulfides in lake sediments (1991)
    Springer
    Biodegradation 14 (1991), S. 193-208 
    Details
    ISSN: 1572-9729
    Keywords: iron oxyhydroxide ; pyrite ; sediment ; sequential extraction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A popular sequential extraction procedure (Tessier et al. 1979) designed t o extract metals partitioned in various sediment phases, was evaluated for its selectivity. Amorphous FeOOH, FeS, and FeS2 were added separately to natural lake sediments and sequentially extracted. The selectivity of the sequential procedure for the added solid phases was evaluated by determining the difference in the mass of Fe extracted from treated and control sediments. In the experiments where sulfide minerals were added, total S was measured in the residual solids in order to confirm selectivity of the method. Concentrations of total carbon remaining in the solid phase after each extraction step were also measured to determine the selectivity of the sequential procedure for carbon. The procedure was moderately selective for Fe added as FeOOH; a mean of 77 ± 12% (p 〈 0.05) of the Fe added was extracted in the step designed to reduce Fe-Mn oxyhydroxides. In experiments where FeS was added, a mean of 69 ± 11% (p 〈 0.05) of the Fe added as FeS was extracted in the fraction designed to oxidize sulfides and organic matter. Approximately 25% of the Fe added as FeS may have been extracted prematurely. Although less precise, total S analyses confirmed that much of the FeS was extracted in the oxidation step, yielding 104 ± 87% (p 〈 0.05) of the S added as FeS. The procedure was highly selective for FeS2; 92 ± 14% (p 〈 0.05) of the Fe added as pyrite was extracted in the sulfide extraction step. Extraction of 80 ± 54% (p 〈 0.05) of S added as pyrite confirmed that FeS2 were selectively extracted in the sulfide extraction step. Carbon in the sediments was also selectively extracted in the oxidation step (77 ± 2.4% of total C; p 〈 0.05). The applications and limitations of sequential extraction procedures as limnological research tools are discussed in light of our results.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00000807
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  • 3
    Electronic Resource
    Electronic Resource
    Contrasting two methods for determining trace metal partitioning in oxidized lake sediments (1992)
    Springer
    Biodegradation 17 (1992), S. 205-219 
    Details
    ISSN: 1572-9729
    Keywords: simultaneous extraction ; sediment ; trace metal partitioning
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A simultaneous (SIM) sediment extraction procedure for low carbonate sediments, which partitions sediment-bound trace metals (Fe, Mn, Zn, Cu, and Cd) into easily reducible (associated with Mn oxides), reducible (associated with Fe oxides) and alkaline extracted (bound to organic) metal is presented. The SIM method was compared to the sequential (SEQ) extraction procedure of Tessier et al. (1979). Both methods showed good agreement for the partitioning of Zn and Cd among the easily reducible, reducible and organic components of sediment. Both methods also showed the same general distribution of Mn, Fe and Cu among the three sediment components, however concentrations of metals recovered by the two methods differed; less Mn and Fe and more Cu was recovered from sediments by the SEQ vs. the SIM procedure. Less recovery of Mn is in part attributed to the loss of this metal in the `in between' reagent rinses required in the SEQ procedure. Greater recovery of Cu by the SEQ vs. the SIM method may be due to the pretreatment of sediment with strong reducing agents prior to the step used for liberating organically bound metals. Advantages of a SIM over the SEQ include rapid sample processing time (i.e. the treatment of 40 samples per day vs. 40 samples in three days), plus minimal sample manipulation. Hence, for partitioning metals into easily reducible, reducible and organic sediment components in sediments low in carbonate, we recommend the use of a SIM extraction over that of a SEQ procedure.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00004042
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  • 4
    Electronic Resource
    Electronic Resource
    Inorganic sulfur turnover in oligohaline estuarine sediments (1993)
    Springer
    Biodegradation 22 (1993), S. 81-105 
    Details
    ISSN: 1572-9729
    Keywords: estuarine ; oligohaline ; sediment ; sulfate reduction ; sulfur ; sulfide oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Inorganic sulfur turnover was examined in oligohaline (salinity 〈 2 g kg-1) Chesapeake Bay sediments during the summer. Cores incubated for 〈 3 hr exhibited higher sulfate reduction (SR) rates (13–58 mmol m-2 d-1) than those incubated for 3–8 hr (3–8 mmol m-2 d-1). SR rates (determined with35SO 4 2- ) increased with depth over the top few cm to a maximum at 5 cm, just beneath the boundary between brown and black sediment. SR rates decreased below 5 cm, probably due to sulfate limitation (sulfate 〈 25 μM). Kinetic experiments yielded an apparent half-saturating sulfate concentration (Ks) of 34 μM, ≈ 20-fold lower than that determined for sediments from the mesohaline region of the estuary. Sulfate loss from water overlying intact cores, predicted on the basis of measured SR rates, was not observed over a 28-hr incubation period. Reduction of35SO 4 2- during diffusion experiments with intact core segments from 0–4 and 5–9 cm horizons was less than predicted by non-steady state diagenetic models based on35SO 4 2- reduction in whole core injection experiments. The results indicate that net sulfate flux into sediments was an order of magnitude lower than the gross sulfur turnover rate. Solid phase reduced inorganic sulfur concentrations were only 2–3 times less than those in sediments from the mesohaline region of the Bay, despite the fact that oligohaline bottom water sulfate concentrations were 10-fold lower. Our results demonstrate the potential for rapid SR in low salinity estuarine sediments, which are inhabited by sulfate-reducing bacteria with a high affinity for sulfate, and in which sulfide oxidation processes replenish the pore water sulfate pool on a time scale of hours.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00002706
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  • 5
    Electronic Resource
    Electronic Resource
    Voltammetric and Spectroscopic Determination of Toxic Metals in Sediments and Sea Water of Salerno Gulf (1999)
    Springer
    Environmental monitoring and assessment 58 (1999), S. 23-37 
    Details
    ISSN: 1573-2959
    Keywords: heavy metal ; sea water ; sediment ; spectroscopy ; voltammetry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract In this present work the distribution of heavy metals in sea water and sediments of the Salerno Gulf is measured. The elements determined were Cu, Pb, Cd, Zn and Hg, employing, as instrumental techniques, either differential pulse anodic stripping voltammetry (DPASV) or graphite furnace atomic absorption spectroscopy (GFAAS). A comparison of the results of the two analytical techniques is also made. Mercury determination was carried out employing the cold vapour atomic absorption spectroscopy (CVAAS) technique, with SnCl2 as the reducing agent. The sample digestion was performed by a new procedure using concentrated suprapure H2SO4–K2Cr2O7 mixture. The accuracy and precision of the analytical procedure were evaluated employing Sea Water BCR-CRM 403 and Estuarine Sediment BCR-CRM 277 as reference materials. Accuracy, expressed as relative error e and precision, expressed as relative standard deviation sr, were in order of 2 to 5%. For both matrices, the detection limits, for all the elements, were in the range μg g-1 to ng g-1.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1006078927576
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  • 6
    Electronic Resource
    Electronic Resource
    Lead in Soil and Sediment in Iqaluit, Nunavut, Canada, and Links with Human Health (2000)
    Springer
    Environmental monitoring and assessment 63 (2000), S. 329-339 
    Details
    ISSN: 1573-2959
    Keywords: bioavailable ; lead ; sediment ; soil
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract This study determined the spatial distribution of soiland of sediment-associated lead in Iqaluit, Nunavut.Samples were collected from the following areas:outside the built-up area of the town to reflectbackground concentrations; known or potential pointsources of lead, such as the Upper Base, the SylviaGrinnell Dump and the Metal Dump (North 40); andresidential and commercial areas of Iqaluit and Apex,a satellite community. In the laboratory, the 〈63 μm sample fraction was analyzed for total lead andbioavailable lead, estimated by non-residual acidextractable lead content. The research findings revealthat elevated levels of bioavailable lead are presentin the study area. Total lead concentrations generallydo not exceed environmental guidelines. However, leadconcentrations in the Sylvia Grinnell Dump, and Apexand Iqaluit grid areas exceed health-based guidelines.The research concludes that there is not a serioushealth hazard posed by lead levels in the soil andsediment in the study area. However, severalenvironmental (elevated lead levels, bioavailableforms of lead and bare soil surfaces) and behaviouralfactors (vigorous and unsupervised play outside) maycreate a risk of lead exposure.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1006253529308
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  • 7
    Electronic Resource
    Electronic Resource
    An Overview of Contaminant-Related Issues Identified by Monitoring in San Francisco Bay (2000)
    Springer
    Environmental monitoring and assessment 64 (2000), S. 409-419 
    Details
    ISSN: 1573-2959
    Keywords: monitoring ; assessment ; water ; sediment ; bioaccumulation ; toxicity ; pesticides ; mercury ; PCB
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract The San Francisco Estuary Regional Monitoring Program for Trace Substances (RMP) began in 1993 and is sponsored by 74 local, state, and federal agencies and companies through their discharge or Bay use permits. The RMP monitors water, sediment, toxicity, and bivalve bioaccumulation at 25 sites in the Bay that are considered to represent "background" conditions. Several major environmental issues have been identified by the RMP. Polychlorinated biphenyls and mercury were often above water quality guidelines, and often occurred in fish tissues above U.S. Environmental Protection Agency (U.S. EPA) screening values. Concentrations do not appear to be decreasing, suggesting continuing inputs. Episodes of aquatic toxicity often occurred following runoff events that transport contaminants into the Bay from urbanized and agricultural portions of the watershed. Sediment toxicity occurred throughout the Bay, and has been correlated with concentrations of specific contaminants (chlordanes, polynuclear aromatic hydrocarbons) at some locations; mixtures of contaminants were probably also important. Since the RMP does not monitor all ecosystem components, assessments of the overall condition of the Bay cannot be made. However, in terms of contamination, the RMP samples suggest that the South Bay, and North Bay sites are moderately contaminated.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1006459605924
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  • 8
    Electronic Resource
    Electronic Resource
    Mobilisation of Heavy Metals in Contaminated Sediments in the River Meuse, The Netherlands (1999)
    Springer
    Water, air & soil pollution 116 (1999), S. 567-586 
    Details
    ISSN: 1573-2932
    Keywords: Complexation ; diffusion ; heavymetals ; mobilisation ; sediment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Due to seasonal variation in bottom-water temperature and degradation of organic matter, the depths of the redox boundaries fluctuate in sediments of the river Meuse. This is reflected by a non-steady state behaviour of heavy metals in the surface sediments. Levels of acid-volatile sulphides suggest that dissolved concentrations of heavy metals in the anoxic pore waters are determined by their respective sulphide phases. However, complexation with dissolved organic ligands may significantly increase dissolved concentrations of heavy metals. In most sediments studied, a distinct peak in dissolved concentrations of heavy metals is measured immediately below the sediment-water interface. This concentration peak may be attributed to degradation of organic matter and oxidation of sulphides. Dissolved concentration gradients indicate that upward diffusion of heavy metals from the sediment can contribute to concentrations in the surface water, although significant effects may be confined to specific locations. In addition, it is shown that release of heavy metals as dissolved species to the surface water is negligible compared to particulate-bound fluxes of heavy metals to the sediment.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1005146927718
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  • 9
    Electronic Resource
    Electronic Resource
    Speciation and Concentrations of Mercury in Certain Coastal Marine Sediments (1998)
    Springer
    Water, air & soil pollution 103 (1998), S. 129-136 
    Details
    ISSN: 1573-2932
    Keywords: coastal pollution ; mercury ; methylation ; methyl mercury ; sediment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Concentrations of total mercury (Hg), methyl Hg and Hg(II) were determined in coastal marine sediments collected from the Baltic, South China and the Bering Seas. Methyl Hg concentrations in sediments were between 0.01 and 2 ng g-1 on a dry weight basis, accounting for only 〈1% of the total Hg concentrations. The percentage of Hg(II) (i.e. available Hg) in total Hg was between 5 and 13 suggesting that most of the Hg in sediments was bound as HgS and/or Hg-humic complexes. Relatively larger proportion of methyl Hg was found in less polluted freshwater sediments than in marine sediments. Methyl Hg concentrations in marine sediments were not found to be correlated with total Hg and/or Hg (II) concentrations.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1004967112178
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  • 10
    Electronic Resource
    Electronic Resource
    Influence of Sediment Preservation on Total Mercury and Methylmercury Analyses (1998)
    Springer
    Water, air & soil pollution 107 (1998), S. 277-288 
    Details
    ISSN: 1573-2932
    Keywords: freezing ; lyophilisation ; mercury ; methylmercury ; sediment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Estuarine and riverine sediments from fourlocations showing different sediment structures wereanalysed as fresh, thawed and lyophilised samples fortotal mercury (TotHg) and methylmercury (MeHg)concentrations, and results were compared to addresseffects of sample preservation on Hg speciation. TotHg was measured by cold vapour atomic absorptionspectrometry (CVAAS). MeHg was isolated bydistillation and ion-exchange and analysed by coldvapour atomic fluorescence spectrometry (CVAFS) afterpreconcentration on a gold trap. No loss of TotHg norMeHg due to lyophilisation was found. Concentrationsof TotHg and MeHg respectively ranged from 92 to 267ng g-1 dw and 1.1 to 2.9 ng g-1 dw in freshsamples, from 94 to 215 ng g-1 dw and 1.1 to 2.8ng g-1 dw in thawed samples, and from 100 to 256ng g-1 dw and 1.2 to 3.1 ng g-1 dw inlyophilised samples. Lyophilised samples showedbetter homogeneity and better MeHg analysisreproducibility compared with wet samples.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1019886606856
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