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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    European journal of soil science 51 (2000), S. 0 
    ISSN: 1365-2389
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: The conduction of water by soil is fundamental to the way in which soils transport nutrients and pollutants into groundwater. The derivation of relations between water flow and void structure has relied on the implicit assumption that water flows through aligned unconnected cylindrical capillary tubes. We describe a three-dimensionally interconnected model of void structure, called Pore-Cor, which simulates the intrusion of a non-wetting fluid and drainage of a wetting fluid. The model is calibrated by fitting it to the water retention curves of a sandy soil at four depths. The experimental drainage pressures are related to the radii of the entries to the voids by the Laplace equation. The necessities of using this equation, and of employing a simplified void geometry, introduce major approximations into the modelling. Nevertheless, the model is sufficiently precise and versatile to predict trends in other properties usefully. It is illustrated in this work by a close correlation between a predicted and experimental change in saturated hydraulic conductivity with depth, and a realistic unsaturated hydraulic conductivity curve. The saturated and unsaturated hydraulic values are shown to be much more realistic than those predicted by the aligned cylinders model. In addition, the simulations by Pore-Cor indicate that the void network within the sandy soil is acting in a structured rather than a random manner. The Pore-Cor model is currently being used to explain the matrix-flow characteristics of tracers and pollutants.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-3017
    Keywords: Ammonia ; in situ monitoring ; crustacea ; heart rate ; flow injection ; landfill leachate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract A portable, computer-aided physiological monitoring system (CAPMON) has been integrated with an automated, flow injection (FI) based chemical monitor to enable continuous, long-term recording of cardiac activity in selected aquatic organisms, and total ammonia concentration in the surrounding environment. Heart rate of the freshwater crayfish Pacifastacus leniusculus was recorded using non-invasive infrared emitter/detectors to transduce heart beat from 4 animals simultaneously. Data were collected continuously and stored on a laptop computer. The chemical monitor incorporated a gas diffusion unit and a solid state photometric detector. Remote control and data processing were accomplished using an in-house designed microcomputer. The instrumentation was fully evaluated in the laboratory and the field and was shown to be capable of operating unattended for periods of at least 1 week. An exposure-response experiment showed that 4 h exposures to concentrations of ammonia greater than 5 mg l-1 had a significant stimulatory effect on heart rate (ANOVA F=7.6; df=5; P〈0.0005). The feasibility of using the system in situ was demonstrated in a 2 week field trial in which the integrated monitors were successfully deployed at a landfill leachate lagoon.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1612-1112
    Keywords: Flow-injection analysis ; Hydrolytic enzymes ; Bioreactor preparations ; Spectrophotometric detection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Automated spectrophotometric flow-injection (FI) procedures for the quantitative determination of the hydrolytic enzymes amylase, xylanase, polygalacturonase and protease, acting on macromolecular substrates, are described. The peptides produced by the protease are derivatized with trinitrobenzene sulphonic acid. For the other enzymes, the reducing sugars produced are derivatized with p-aminobenzoylhydrazide (PABH). The FI manifold design allows the choice of any required detetion, range between 0.1 U ml−1 and several hundred U ml−1. Two FI manifold designs are proposed; one optimizes, sample throughput at a high sensitivity level by incorporating several parallel incubation coils, the other minimizes sample volume at a low sensitivity level and facilitates, automation. The instrumentation is largely based on commercial HPLC equipment.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 32 (1991), S. 483-484 
    ISSN: 1612-1112
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Publication Date: 2014-01-27
    Description: As part of the PREDICT Tamar Workshop, the toxicity of estuarine waters in the Tamar Estuary (southwest England) was assessed by integration of metal speciation determination with bioassays. High temporal resolution metal speciation analysis was undertaken in situ by deployment of a Voltammetric In situ Profiling (VIP) system. The VIP detects Cd (cadmium), Pb (lead) and Cu (copper) species smaller than 4 nm in size and this fraction is termed 'dynamic' and considered biologically available. Cadmium was mainly present in the dynamic form and constituted between 56 and 100 of the total dissolved concentration, which was determined subsequently in the laboratory in filtered discrete samples. In contrast, the dynamic Pb and Cu fractions were less important, with a much larger proportion of these metals associated with organic ligands and/or colloids (45-90 Pb and 46-85 Cu), which probably reduced the toxicological impact of these elements in this system. Static toxicity tests, based on the response of Crassostrea gigas larva exposed to discrete water samples showed a high level of toxicity (up to 100 abnormal development) at two stations in the Tamar, particularly during periods of the tidal cycle when the influence of more pristine coastal water was at its lowest. Competitive ligand-exchange Cu titrations showed that natural organic ligands reduced the free cupric ion concentration to levels that were unlikely to have been the sole cause of the observed toxicity. Nonetheless, it is probable that the combined effect of the metals determined in this work contributed significantly to the bioassay response. © 2011 Elsevier Ltd.
    Type: Article , PeerReviewed
    Format: text
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  • 6
    Publication Date: 2014-02-05
    Description: The distribution of size fractionated dissolved iron (DFe, 〈0.2 μm) species was determined in the upper water column (0-150 m) of the Canary Basin (25-32°N and 18-24°W) on a research cruise in October 2002. A DFe concentration gradient resulting from a decrease in both soluble iron (SFe, 〈0.02 μm) and colloidal iron (CFe, 0.02-0.2 μm) was shown to extend from the coast of North West Africa into the oligotrophic gyre (varying from ∼1 nM in the shelf region to 0.15 nM in the most off shore waters). At the time of this study, the dominant dissolved Fe input to the region was deduced to be the advection of shelf and upwelled waters rather than Saharan dust deposition.SFe and CFe fractions had mean concentrations (± one standard deviation) of 0.25 ± 0.11 and 0.21 ± 0.16 nM, respectively (n = 58). Colloidal iron formed a highly variable fraction of DFe (ca. 0-80, mean of 42) in the region but was less variable in the low iron, oligotrophic intermediate waters (0.18 ± 0.06 nM, 31.7°N, 22.0°W, 0-1300 m depth). The high variability found at the most productive near-shelf stations was driven by biological processing and mixing of different water masses. In contrast, less variability between SFe and CFe at the remote off shore stations suggested that vertical variations in the water column were controlled more by chemical partitioning and vertical particle fluxes with evidence of preferential biological uptake and/or removal of SFe in the most remote surface waters. © 2010.
    Type: Article , PeerReviewed
    Format: text
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  • 7
    Publication Date: 2014-01-27
    Description: A detailed investigation into the performance of two flow injection-chemiluminescence (FI-CL) manifolds (with and without a preconcentration column) for the determination of sub-nanomolar dissolved iron (Fe(II) + Fe(III)), following the reduction of Fe(III) by sulphite, in seawater is described. Kinetic experiments were conducted to examine the efficiency of reduction of inorganic Fe(III) with sulphite under different conditions and a rigorous study of the potential interference caused by other transition metals present in seawater was conducted. Using 100 μM concentrations of sulphite a reduction time of 4 h was sufficient to quantitatively reduce Fe(III) in seawater. Under optimal conditions, cobalt(II) and vanadium(IV)/(III) were the major positive interferences and strategies for their removal are reported. Specifically, cobalt(II) was masked by the addition of dimethylglyoxime to the luminol solution and vanadium(IV) was removed by passing the sample through an 8-hydroxyquinoline column in a low pH carrier stream. Manganese(II) also interfered by suppression of the CL response but this was not significant at typical open ocean concentrations. © 2009 Elsevier B.V. All rights reserved.
    Type: Article , PeerReviewed
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  • 8
    Publication Date: 2020-07-27
    Description: The marine biogeochemistries of carbon and nitrogen have come under increased scrutiny because of their close involvement in climate change and coastal eutrophication. Recent studies have shown that the high-temperature combustion (HTC) technique is suitable for routine analyses of dissolved organic matter due to its good oxidation efficiency, high sensitivity, and precision. In our laboratory, a coupled HTC TOC-NCD system with a sample changer was used for the automated and simultaneous determination of dissolved organic carbon (DOC) and total dissolved nitrogen (TDN)in seawater samples. TOC control software was used for TOC instrument control, DOC data acquisition, and data analysis. TDN data acquisition and manipulation was undertaken under LabVIEW. The combined system allowed simultaneous determination of DOC and TDN in the same sample using a single injection and provided low detection limits and excellent linear ranges for both DOC and TDN. The risk of contamination has been remarkably reduced due to the minimal sample manipulation and automated analyses. The optimised system provided a reliable tool for the routine determination of DOC and TDN in marine waters. © 2005 Hindawi Publishing Corporation.
    Type: Article , PeerReviewed
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  • 9
    Publication Date: 2014-02-04
    Description: The effects of dissolved organic compounds on the determination of nanomolar concentrations of Fe(II) have been compared using two luminol-based flow injection chemiluminescence (FI-CL) methods. One used the direct injection of sample into the luminol reagent stream, and the other incorporated on-line solid-phase extraction of the analyte on an 8-hydroxyquinoline microcolumn. The CL signals from analyses of dissolved iron species (Fe(II) and Fe(III)) with model ligands and organic compounds were examined in high-purity water and seawater. The organic compounds included natural reducing agents (e.g., ascorbic acid), nitrogen σ-donor/π-acceptor compounds (e.g., 1,4-dipyridine, protoporphyrin IX), aromatic compounds (e.g., 1,4-dihydroxybenzene), synthetic iron chelators (e.g., EDTA), and natural iron binding compounds (e.g., desferrioxamine B, ferrichrome A). Fe(II) determinations for both luminol FI-CL methods were affected by submicromolar concentrations of redox-active compounds, strong iron binding ligands (i.e., log KFeL > 6), and compounds with electron-donating functional groups in both high-purity water and seawater. This was due to reactions between organic molecules and iron species before and during analysis, rather than chemiluminescence caused by the individual organic compounds. In addition, the effects of strong ligands and size speciation on Fe(II) recoveries from seawater following acidification (pH 2) and reduction (100 μM sodium sulfite) were investigated. © 2005 American Chemical Society.
    Type: Article , PeerReviewed
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  • 10
    Publication Date: 2017-05-30
    Description: Siderophore type chelates were isolated from nutrient enriched seawater collected from coastal and near shore environments and detected using a novel high performance liquid chromatography-electrospray ionisation-mass spectrometric technique. Seawater was enriched with added glucose, ammonia and phosphate, and incubated for four days. Seven different siderophore type compounds were detected in the extracted supernatants and tentatively identified based on mass numbers and spectra. The compounds comprised two groups, the ferrioxamines and the amphibactins. They were produced at typical coastal iron concentrations (total dissolved iron=2.9±1.4 and 2.2±0.1 nM) both in the presence and absence of the iron chelating ligand ethylene diamine-N,N′-diacetic acid. © 2004 Elsevier B.V. All rights reserved.
    Type: Article , PeerReviewed
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