High‐temporal resolution fluvial sediment source fingerprinting with uncertainty: a Bayesian approach

This contribution addresses two developing areas of sediment fingerprinting research. Specifically, how to improve the temporal resolution of source apportionment estimates whilst minimizing analytical costs and, secondly, how to consistently quantify all perceived uncertainties associated with the sediment mixing model procedure. This first matter is tackled by using direct X‐ray fluorescence spectroscopy (XRFS) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) analyses of suspended particulate matter (SPM) covered filter papers in conjunction with automatic water samplers. This method enables SPM geochemistry to be quickly, accurately, inexpensively and non‐destructively monitored at high‐temporal resolution throughout the progression of numerous precipitation events. We then employed a Bayesian mixing model procedure to provide full characterization of spatial geochemical variability, instrument precision and residual error to yield a realistic and coherent assessment of the uncertainties associated with source apportionment estimates. Applying these methods to SPM data from the River Wensum catchment, UK, we have been able to apportion, with uncertainty, sediment contributions from eroding arable topsoils, damaged road verges and combined subsurface channel bank and agricultural field drain sources at 60‐ and 120‐minute resolution for the duration of five precipitation events. The results presented here demonstrate how combining Bayesian mixing models with the direct spectroscopic analysis of SPM‐covered filter papers can produce high‐temporal resolution source apportionment estimates that can assist with the appropriate targeting of sediment pollution mitigation measures at a catchment level. © 2015 The Authors. Earth Surface Processes and Landforms published by John Wiley & Sons Ltd.     

Sediment contamination in floodplains and alluvial terraces as an historical record of gold exploitation in the Carmo River basin,Southeast Quadrilátero Ferrífero,Minas Gerais,Brazil

This paper describes the geochemistry of sediment samples placed in floodplains and alluvial terraces downstream from gold mines in the Carmo River basin, Quadrilátero Ferrífero, Minas Gerais, Brazil. The geochemistry signature Na₂O, K₂O, SiO₂, CaO, MgO, Al₂O₃, Fe₂O₃, TiO₂, P₂O₅, Mn, As, Cu, Zn, Ba, Ni, Cr, S, Co were analyzed in different facies from stratigraphic profiles. As, Cu, Zn, and Mn anomalies are mainly associated with the clayed facies deposited in floodplains and oxbow lakes, and with coarse‐sediment facies deposited in the channel. The facies were accumulated by the gold exploitation activity in the region. The contamination of As, Cu, and Zn was controlled by minerals such as iron oxides and hydroxides (hematite, magnetite, and mainly goethite), manganese oxides, and sulfide‐rich minerals. The As‐bearing sediments of the region characterize one of the most As contaminated area of Brazil. Their main source is associated with gold exploration in the last three centuries.     

Video‐based gravel transport measurements with a flume mounted light table

The study of bedload transport processes is constrained by an inability to monitor the mass, volume and grain size distribution of sediment in transport at high temporal frequencies. Building upon a previously published design, we have integrated a high‐resolution (1392 × 1024 pixels) video camera with a light table to continuously capture images of 2–181 mm material exiting a flume. The images are continuously recorded at a rate of 15 to 20 frames per second and are post‐processed using LabView^(?) software, yielding continuous grain‐size‐specific transport information on a per second basis. The video capture rate is sufficient to record multiple images of each grain leaving the flume so that particle velocities can be measured automatically. No manual image processing is required. After calibration the method is accurate and precise for sediment in the 2 mm through to 45 mm grain size classes compared with other means of measuring bedload. Based on a set of validation samples, no statistically significant difference existed between the D₁₀, D₁₆, D₂₅, D₅₀, D₇₅, D₈₄, D₉₀ and D₉₅ determined by sieving captured samples and the D_i values determined with the system. On average the system overpredicted transport by 4 per cent (n = 206, SD = 42%). This error can be corrected easily by simply weighing the mass of sediment that leaves the flume. The technology is relatively inexpensive and provides high‐resolution data on coarse sediment transport out of a flume. Copyright © 2008 John Wiley & Sons, Ltd.     

Tracer properties of eroded sediment and source material

This paper examines the conservativeness of tracers through the sediment generation process. This is done by comparing a selection of tracer properties of sediment eroded from large plots by simulated rainfall, with the corresponding properties of the source materials within the plots. Sediment was generated using three simulated rainfall events for each of five selected erosion source types in the Tarago catchment, Victoria, Australia. As there were particle size and organic content differences between the source material and the generated sediment, the measured tracer properties of the source material were corrected for these differences. The possible role of analytical errors in this investigation was also addressed. The geochemical property, concentration of Fe₂O₃, was not conservative for any of the process sources investigated. Concentration of Al₂O₃ was not conservative for three of the four process sources investigated, and the sum of molecular proportions of CaO**, Na₂O, K₂O and Al₂O₃ was not conservative for two of the four process sources investigated. Mineral magnetic properties, IRM₈₅₀ and χ were also found to be not conservative, although this may be the result of the complex relationship between particle size and mineral magnetic properties not being adequately accommodated in this analysis. The radionuclide tracers, ¹³⁷Cs and ²¹⁰Pb_ex, were found to be conservative through the sediment generation process. Copyright © 2002 John Wiley & Sons, Ltd.     

Relevant Reducing Agents in Remediation Fe0/H2O Systems

Metallic iron (Fe⁰) is often reported as a reducing agent for environmental remediation. There is still controversy as to whether Fe⁰ plays any significant direct role in the process of contaminant reductive transformation. The view that Fe⁰ is mostly a generator of reducing agents (e.g. H, H₂ and Fe^II) and Fe oxyhydroxides has been either severely refuted or just tolerated. The tolerance is based on the simplification that, without Fe⁰, no secondary reducing agents could be available. Accordingly, Fe⁰ serves as the original source of electron donors (including H, H₂ and Fe^II). The objective of this communication is to refute the named simplification and establish that quantitative reduction results from secondary reducing agents. For this purpose, reports on aqueous contaminant removal by Al⁰, Fe⁰ and Zn⁰ are comparatively discussed. Results indicated that reduction may be quantitative in aqueous systems containing Fe⁰ and Zn⁰ while no significant reduction is observed in Al⁰/H₂O systems. Given that Al⁰ is a stronger reducing agent than Fe⁰ and Zn⁰, it is concluded that contaminant reduction in Fe⁰/H₂O systems results from synergic interactions between H/H₂ and Fe^II within porous Fe oxyhydroxides. This conclusion corroborates the operating mode of Fe⁰ bimetallics as H/H₂ producing systems for indirect contaminant reduction.     

Towards continuous long-term measurements of suspended particulate matter (SPM) in turbid coastal waters

The dynamics of sediment transport in the East Frisian Wadden Sea are important for the coastal zone and for ecosystem functioning. The tidal inlets between the East Frisian islands connect the back-barrier intertidal flats to the North Sea. Here, concentrations of suspended particulate matter (SPM) in the water column are highly variable, depending on weather conditions and tides. In order to estimate the nature and quantity of sediment transport, in situ measurements were carried out at a Time Series Station in the tidal inlet between the islands of Spiekeroog and Langeoog. This study shows the suitability of multispectral transmissometry (MST) for obtaining long-term SPM measurements with high resolution. The comparability of this technique to the standard filter method and the laser diffraction method [laser in situ scattering and transmissometry (LISST)] is demonstrated. In addition, the Junge coefficients derived from both MST and LISST measurements are compared. A time series of SPM data covering nearly 4 months is presented. As a major result, the data reveal that a single storm surge can have less impact on SPM dynamics than longer-lasting gales. This high-resolution long-term data set is very valuable for modelling suspended matter flux. It also provides background information for studying the influence of SPM dynamics on coastal sediments.     

In situ characterization of grain‐scale fluvial morphology using Terrestrial Laser Scanning

The grain‐scale morphology of fluvial sediments is an important control on the character and dynamics of river systems; however current understanding of its role is limited by the difficulties of robustly quantifying field surface morphology. Terrestrial Laser Scanning (TLS) offers a new methodology for the rapid acquisition of high‐resolution and high‐precision surface elevation data from in situ sediments. To date, most environmental and fluvial applications of TLS have focused on large‐scale systems, capturing macroscale morphologies. Application of this new technology at scales necessary to characterize the complexity of grain‐scale fluvial sediments therefore requires a robust assessment of the quality and sources of errors in close‐range TLS data. This paper describes both laboratory and field experiments designed to evaluate close‐range TLS for sedimentological applications and to develop protocols for data acquisition. In the former, controlled experiments comprising high‐resolution scans of white, grey and black planes and a sphere were used to quantify the magnitude and source of three‐dimensional (3D) point errors resulting from a combination of surface geometry, reflectivity effects and inherent instrument precision. Subsequently, a methodology for the collection and processing of grain‐scale TLS data is described through an application to a coarse grained gravel system, the River Feshie (D₅₀ 32 to 63 mm). This stepwise strategy incorporates averaging repeat scans and filtering scan artefact and non‐surface points using local 3D search algorithms. The sensitivity of the results to the filter parameter values are assessed by careful internal validation of Digital Terrain Models (DTMs) created from the resulting point cloud data. The transferability of this methodology is assessed through application to a second river, Bury Green Brook, dominated by finer gravel (D₅₀ 18 to 33 mm). The factor limiting the resolution of DTMs created from this second dataset was found to be the relative sizes of the laser footprint and smallest grains. Copyright © 2009 John Wiley & Sons, Ltd.     

Variation of nutrients in response to the highly dynamic suspended particulate matter in the Changjiang (Yangtze River) plume

During four surveys at spring and neap tides in July and November 2005, continuous observations were conducted at four stations adjacent to the Changjiang (Yangtze River) mouth. The observation times lasted for 26 h that covered two consecutive semidiurnal cycles. Resuspension events and subsequently enhancements of suspended particulate matter (SPM) were commonly observed within a tidal cycle. Although nutrients (SiO₃²⁻, NO₃⁻, and PO₄³⁻) were primarily governed by salinity, their statistically significant correlations with SPM could always be extracted after partial correlation analysis. Three parameter (salinity, SPM, nutrients) regressions generally produced better results of simulating nutrient concentrations than two parameter (salinity and nutrients) regressions, although compared to the latter, the former R² values were elevated by no more than 13%. The partial correlation between SPM and a specific nutrient could be either positive or negative in different surveys, suggesting SPM influenced the nutrients in different ways under various conditions. The minor (albeit statistically significant) impacts of highly dynamic SPM on nutrients might be ascribed to the short duration time of resuspension events and estuarine mixing process, together with the complex nature of circulation in the Changjiang plume seawater.     

Cross-section through the frontal Japan Trench subduction zone: Geochemical evidence for fluid flow and fluid–rock interaction from DSDP and ODP pore waters and sediments

Abstract Fluids and sediments from Deep Sea Drilling Project/Ocean Drilling Program Legs (56, 57, 87 and 186) along a transect extending from the subducting plate, across the midslope and upper slope of the Japan Trench forearc were analyzed for B and B isotopes in order to assess their composition and fluid–sediment interaction. At the reference Site 436 on the subducting plate, changes in B contents and B isotopes are controlled by the lithology and diagenesis only. The midslope Sites 440 and 584 showed stronger variations in the B geochemistry, which can be related to diagenesis and tectonic dewatering along faults. The strongest changes in the B geochemistry were observed on the upper slope Sites 1150 and 1151, where profound down‐hole freshening (chlorinities as low as ～310 mmol) coincides with a B enrichment (up to 9.3 × seawater concentration). The B isotope pore fluid profile of Site 1150 displayed a bimodal variation with depth, first increasing to values more positive than seawater, then shifting to lower signatures typical for deep‐seated fluids, whereas Site 1151 showed a constant B decrease with depth. Sites 1150 and 1151 sediments showed B increases with depth to values as high as ～164 p.p.m. and isotopic compositions ranging from ～+4 to ?9‰. A linear decrease in B_solid/B_fluid ratio, suggests that B geochemistry of the upper slope sites is controlled by fluid–rock interaction and deep‐seated fluid flow, whereas constant B_solid/B_fluid ratios were observed at the reference site on the incoming plate. This fluid overprint is probably caused by normal faults in the sediment cover which might be interconnected to deep thrusts in the underlying Cretaceous accreted wedge. This suggests that the erosive Japan Trench margin is characterized by back‐flux of deep‐seated, B‐enriched fluids into the ocean, which is facilitated by extensional normal faulting as a result of tectonic erosion and subsidence.     

The performance of grass filter strips in controlling high‐concentration suspended sediment from overland flow under rainfall/non‐rainfall conditions

There is little information on the performance of vegetative filter strips (VFS) in filtering high‐concentration sediment from subcritical overland flow. Flume experiments on simulated grass strips were conducted using combinations of three slope gradients (3°, 9° and 15°), five 1‐m‐wide slope positions (from upslope to downslope), two flow rates (60 and 20 L min^‐1 m^‐1) and sediment concentrations of 100–300 kg m^‐3 under simulated rainfall and non‐rainfall conditions. The results showed that sediment deposition efficiency increased with VFS width as a power function. Rainfall significantly reduced sediment deposited within VFS. Higher sediment concentration corresponded to a larger sediment deposition load but reduced deposition efficiency. Flow rate had a negative effect on deposition efficiency but no effect on deposition load. Sediments were more easily deposited at the upper slope position than downslope, and the upper slope position had a higher percentage of coarse sediments. The deposited sediment had significantly greater median diameters (D₅₀) than the inflow sediment. A greater proportion of coarse sediments larger than 25 µm in diameter were deposited, and particles smaller than 1 µm and of 10–25 µm had a better deposition performance than particles of 1–10 µm. Rainfall reduced the deposited sediment D₅₀ at a slope gradient of 3° and had no significant influence on it at 9° or 15°. A higher sediment concentration led to a smaller D₅₀ of the deposited sediment. Rainfall had no significant effect on overland flow velocity. Both the deposited sediment load and D₅₀ decreased with increasing flow velocity, and flow velocity was the most sensitive factor impacting sediment deposition. The results from this study should be useful to control sediment flowing into rivers in areas with serious soil erosion. Copyright © 2013 John Wiley & Sons, Ltd.     

Geochemical characteristics and Sr‐Nd‐Hf isotope compositions of Late Triassic post‐collisional A‐type granites in Sarudik,SW Sumatra,Indonesia

Late Triassic A‐type granites are identified in this study in Sarudik, SW Sumatra. We present new data on zircon U–Pb geochronology, whole‐rock major and trace elements and Sr‐Nd‐Hf isotope geochemistry, aiming to study their petrogenesis and tectonic implications. LA‐ICP‐MS U–Pb dating of zircon separated from one biotite monzogranite sample yields a concordia age of 222.6 ±1.0 Ma, indicating a Late Triassic magmatic event. The studied granites are classified as weakly peralumious, high‐K calc‐alkaline granites. They exhibit high SiO₂, K₂O + Na₂O, FeO/(FeO + MgO) and Ga/Al ratios and low Al₂O₃, CaO, MgO, P₂O₅ and TiO₂ contents, with enrichment of Rb, Th and U and depletion of Ba, Sr, P and Eu, showing the features of A‐type granites. The granites have zircon ε_Hf(t) values from ?4.6 to ?0.4 and whole‐rock ε_Nd(t) values from ?5.51 to ?4.98, with Mesoproterozoic T_DM2 ages (1278–1544 Ma) for both Hf and Nd isotopes. Geochemical and isotopic data suggest that the source of these A‐type granites is the Mesoproterozoic continental crust, without significant incorporation of mantle‐derived component, and their formation is controlled by subsequent fractional crystallization. The Sarudik A‐type granites are further assigned to A2‐type formed in post‐collisional environment. Combined with previous knowledge on the western SE Asia tectonic evolution, we conclude that the formation of the Late Triassic A‐type granites is related to the post‐collisional extension induced by the crustal thickening, gravitational collapse, and asthenosphere upwelling following the collision between the Sibumasu and the East Malaya Block.     

Preparation of Magnetic Hydroxyapatite and Their Use as Recyclable Adsorbent for Phenol in Wastewater

Magnetic hydroxyapatite (HAP), which combined superparamagnetic Fe₃O₄ nanoparticles and HAP, composite materials were prepared by ultrasound method in this paper. It has also been found that these materials have the ability to adsorb phenol in wastewater. The magnetic materials were investigated by scanning electron microscope, X‐ray diffraction (XRD), Fourier transform infrared spectroscopy, thermal gravimetric analysis, vibrating sample magnetometer, and N₂ adsorption in order to elucidate the morphology, structure, and other properties. When the prepared magnetic materials were calcined at 200°C, the prepared Fe₃O₄ was oxidized to Fe₂O₃, possessing loose‐shaped holes with a high specific area of 325.2 m²/g, a magnetization intensity of 12.5 emu/g, and the N₂ adsorption isotherm belongs to porous adsorption type I. Moreover, the magnetic HAP can adsorb 90% phenol in wastewater. This means that it is an excellent recyclable phenol sorbent for sewage treatment. Experiments confirmed that the Freundlich adsorption isotherms model applies to lower phenol concentrations (0–50 mg/L), while for high phenol concentrations (50–500 mg/L) the Langmuir adsorption isotherms model fits. The magnetic sorbents have the capacity to regenerate after reaching adsorption saturation using ethanol as eluant and external magnetic field as separation unit. The efficiency of adsorption was reduced only by 10% over a six time use period.     

Pyroxene-garnet solid-solution equilibria in the systems Mg4Si4O12Mg3Al2Si3O12 and Fe4Si4O12Fe3Al2Si3O12 at high pressures and temperatures

Pyroxene-garnet solid-solution equilibria have been studied in the pressure range 41–200 kbar and over the temperature range 850–1,450°C for the system Mg₄Si₄O₁₂Mg₃Al₂Si₃O₁₂, and in the pressure range 30–105 kbar and over the temperature range 1,000–1,300°C for the system Fe₄Si₄O₁₂Fe₃Al₂Si₃O₁₂. At 1,000°C, the solid solubility of enstatite (MgSiO₃) in pyrope (Mg₃Al₂Si₃O₁₂) increases gradually to 140 kbar and then increases suddenly in the pressure range 140–175 kbar, resulting in the formation of a homogeneous garnet with composition Mg₃(Al_0.8Mg_0.6Si_0.6)Si₃O₁₂. In the MgSiO₃-rich field, the three-phase assemblage of β- or γ-Mg₂SiO₄, stishovite and a garnet solid solution is stable at pressures above 175 kbar at 1,000°C. The system Fe₄Si₄O₁₂Fe₃Al₂Si₃O₁₂ shows a similar trend of high-pressure transformations: the maximum solubility of ferrosilite (FeSiO₃) in almandine (Fe₃Al₂Si₃O₁₂) forming a homogeneous garnet solid solution is 40 mol% at 93 kbar and 1,000°C.If a pyrolite mantle is assumed, from the present results, the following transformation scheme is suggested for the pyroxene-garnet assemblage in the mantle. Pyroxenes begin to react with the already present pyrope-rich garnet at depths around 150 km. Although the pyroxene-garnet transformation is spread over more than 400 km in depth, the most effective transition to a complex garnet solid solution takes place at depths between 450 and 540 km. The complex garnet solid solution is expected to be stable at depths between 540 and 590 km. At greater depths, it will decompose to a mixture of modified spinel or spinel, stishovite and garnet solid solutions with smaller amounts of a pyroxene component in solution.     

Mineralogical and geochemical study of a newly discovered mafic granulite, northwest China: Implications for tectonic evolution of the Altay Orogenic Belt

Abstract A mafic granulite body was newly discovered in the Altay Orogenic Belt, northwest China. The rocks comprise a suite of coarse‐grained and fine‐grained granulites. Orthopyroxenes (hypersthenes) in the rocks have high X_Mg and low Al₂O₃ contents, whereas clinopyroxenes have low TiO₂ and Al₂O₃ contents. Amphiboles and biotites have a high Mg/(Mg + Fe²⁺) ratio and low contents of F and Cl. The peak metamorphic pressure–temperature (P–T) conditions are estimated as 750–780°C and 6–7 kbar, and retrograde P–T conditions are in the range of 590–620°C and 2.3–3.7 kbar, indicating significant decompression. Metamorphic reactions and P–T estimates define a clockwise P–T path. Geochemically, the rocks are high in Mg/(Mg + Fe) and Al₂O₃, depleted in U, Th, K and Rb, and characterized by light rare earth element enrichment and a weak positive Eu anomaly. The Altay mafic granulite shows depleted Nb, P and Ti contents in the mid‐oceanic ridge basalt normalized spider diagram. The geochemical characteristics suggest that the protolith of the Altay mafic granulite was calc‐alkaline basalt and andesite with an island‐arc affinity. The rock has a high ¹⁴³Nd/¹⁴⁴Nd ratio with ?Nd(0) > 0, indicating derivation from a mantle‐depleted source. In the present study, a two‐stage model for the evolution of the Altay mafic granulite is proposed: an early stage in which calc‐alkaline basalt and andesite with island‐arc affinity were subducted into a deeper level of the crust and subjected to granulite‐facies metamorphism generating the mafic granulite, followed by the later stage exhumation of the system into the upper crust by the late Paleozoic thrusting.     

Iron oxidation state in lower mantle mineral assemblages: II. Inclusions in diamonds from Kankan, Guinea

Inclusions of ferropericlase and former (Mg,Fe)(Si,Al)O₃ perovskite in diamonds from Kankan, Guinea believed to originate in the lower mantle were studied using Mössbauer spectroscopy to determine Fe³⁺/ΣFe. Fe³⁺ concentration in the (Mg,Fe)(Si,Al)O₃ inclusion is consistent with empirical relations relating Fe³⁺/ΣFe to Al concentration, supporting the inference that it crystallised in the perovskite structure at lower mantle conditions. In ferropericlase there is a nearly linear variation of trivalent cation abundance with monovalent cation abundance, suggesting a substitution of the form Na_0.5M_0.5³⁺O (M=Fe³⁺, Cr³⁺, Al³⁺). Excess positive charge is likely balanced by cation vacancies, where their abundance is observed to increase with increasing iron concentration, consistent with high-pressure experiments. The abundance of cation vacancies is related to oxygen fugacity, where ferropericlase inclusions from Kankan and São Luiz (Brazil) are inferred to have formed at conditions more oxidising than Fe-(Mg,Fe)O equilibrium, but more reducing than Re-ReO₂ equilibrium. Fe²⁺/Mg partition coefficients between (Mg,Fe)(Si,Al)O₃ and ferropericlase were calculated for inclusions co-existing in the same diamond using Mössbauer data and empirical relations based on high-pressure experimental work. Most values are consistent with high-pressure experiments, suggesting that these inclusions equilibrated at lower mantle conditions. The measured ferropericlase Fe³⁺ concentrations are consistent with diamond formation in a region of redox gradients, possibly arising from the subduction of oxidised material into reduced lower mantle. Reduction of carbonate to form ferropericlase and diamond is consistent with a slight shift of Kankan δ¹³C values to isotopically heavy compositions compared to the worldwide dataset, and could supply the oxygen necessary to satisfy the high Fe³⁺ concentration in (Mg,Fe)(Si,Al)O₃ perovskite, as well as account for the high proportion of ferropericlase in the lower mantle paragenesis. The heterogeneity of lower mantle diamond sources indicates that the composition of lower mantle diamonds do not necessarily reflect those of the bulk mantle.     

Effect of Pumice and Sand on the Sustainability of Granular Iron Beds for the Aqueous Removal of CuII,NiII, and ZnII

Current knowledge of the basic principles underlying the design of Fe⁰ beds is weak. The volumetric expansive nature of iron corrosion was identified as the major factor determining the sustainability of Fe⁰ beds. This work attempts to systematically verify developed concepts. Pumice and sand were admixed to 200 g of Fe⁰ in column studies (50:50 volumetric proportion). Reference systems containing 100% of each material have been also investigated. The mean grain size of the used materials (in mm) were 0.28 (sand), 0.30 (pumice), and 0.50 (Fe⁰). The five studied systems were characterized (i) by the time dependent evolution of their hydraulic conductivity (permeability) and (ii) for their efficiency for aqueous removal of Cu^II, Ni^II, and Zn^II (about 0.3 mM of each). Results showed unequivocally that (i) quantitative contaminant removal was coupled to the presence of Fe⁰, (ii) additive admixture lengthened the service life of Fe⁰ beds, and (iii) pumice was the best admixing agent for sustaining permeability while the Fe⁰/sand column was the most efficient for contaminant removal. The evolution of the permeability was well‐fitted by the approach that the inflowing solution contained dissolved O₂. The achieved results are regarded as starting point for a systematic research to optimize/support Fe⁰ filter design.     

Application of the continuous wavelet transform on seismic data for mapping of channel deposits and gas detection at the CO2SINK site, Ketzin, Germany

Conventional seismic data are band limited and therefore, provide limited geological information. Every method that can push the limits is desirable for seismic data analysis. Recently, time‐frequency decomposition methods are being used to quickly extract geological information from seismic data and, especially, for revealing frequency‐dependent amplitude anomalies. Higher frequency resolution at lower frequencies and higher temporal resolution at higher frequencies are the objectives for different time‐frequency decomposition methods. Continuous wavelet transform techniques, which are the same as narrow‐band spectral analysis methods, provide frequency spectra with high temporal resolution without the windowing process associated with other techniques. Therefore, this technique can be used for analysing geological information associated with low and high frequencies that normally cannot be observed in conventional seismic data. In particular, the continuous wavelet transform is being used to detect thin sand bodies and also as a direct hydrocarbon indicator. This paper presents an application of the continuous wavelet transform method for the mapping of potential channel deposits, as well as remnant natural gas detection by mapping low‐frequency anomalies associated with the gas. The study was carried out at the experimental CO₂ storage site at Ketzin, Germany (CO₂SINK). Given that reservoir heterogeneity and faulting will have significant impact on the movement and storage of the injected CO₂, our results are encouraging for monitoring the migration of CO₂ at the site. Our study confirms the efficiency of the continuous wavelet transform decomposition method for the detection of frequency‐dependent anomalies that may be due to gas migration during and after the injection phase and in this way, it can be used for real‐time monitoring of the injected CO₂ from both surface and borehole seismics.     

Significance of particle interaction to the modelling of cohesive sediment transport in rivers

Aggregation processes of fine sediments have rarely been integrated in numerical simulations of cohesive sediment transport in riverine systems. These processes, however, can significantly alter the hydrodynamic characteristics of suspended particulate matter (SPM), modifying the particle settling velocity, which is one of the most important parameters in modelling suspended sediment dynamics. The present paper presents data from field measurements and an approach to integrate particle aggregation in a hydrodynamic sediment transport model. The aggregation term used represents the interaction of multiple sediment classes (fractions) with corresponding multiple deposition behaviour. The k–ε–turbulence model was used to calculate the coefficient of vertical turbulent mixing needed for the two‐dimensional vertical‐plane simulations. The model has been applied to transport and deposition of tracer particles and natural SPM in a lake‐outlet lowland river (Spree River, Germany). The results of simulations were evaluated by comparison with field data obtained for two levels of river discharge. Experimental data for both discharge levels showed that under the prevailing uniform hydraulic conditions along the river reach, the settling velocity distribution did not change significantly downstream, whereas the amount of SPM declined. It was also shown that higher flow velocities (higher fluid shear) resulted in higher proportions of fast settling SPM fractions. We conclude that in accordance with the respective prevailing turbulence structures, typical aggregation mechanisms occur that continuously generate similar distribution patterns, including particles that settle toward the river bed and thus mainly contribute to the observed decline in the total SPM concentration. In order to determine time‐scales of aggregation and related mass fluxes between the settling velocity fractions, results of model simulations were fitted to experimental data for total SPM concentration and of settling velocity frequency distributions. The comparison with simulations for the case of non‐interacting fractions clearly demonstrated the practical significance of particle interaction for a more realistic modelling of cohesive sediment and contaminant transport. Copyright © 2004 John Wiley & Sons, Ltd.     

Lithological and hydrological controls on water composition: evaporite dissolution and glacial weathering in the south central Andes of Argentina (33°–34°S)

Lithological and hydrological influence on fluvial physical and chemical erosion was studied in a glacierized sedimentary basin with high evaporite presence. Suspended particulate matter (SPM), total dissolved solids (TDS) and major ion concentrations were analysed for 2 years of different hydrologic condition: (i) 2009–2010, Q = 100% average; and (ii) 2010–2011, Q = 60% average. Annual hydrograph was simple regime‐type with one peak in summer related to snow melting. The intra‐annual SPM and TDS variations were directly and inversely associated to Q, respectively. Snow chemistry showed continental influence (Na⁺/Ca²⁺ = 0.17), and atmospheric input of TDS was <1% of the total exported flux. River water was highly concentrated in Ca²⁺ and SO₄²⁻ (~4 mmol l⁻¹) and in Na⁺ and Cl⁻ (~3 mmol l⁻¹). Ca²⁺/SO₄²⁻ and Na⁺/Cl⁻ molar ratios were ~1 and related to Q, directly and inversely, respectively. Major ion relationships suggest that river chemistry is controlled by evaporite (gypsum and halite) dissolution having a summer input from sulfide oxidation and carbonate dissolution, and a winter input from subsurface flow loaded with silicate weathering products. This variation pattern resulted in nearly chemostatic behaviour for Ca⁺, Mg²⁺ and SO₄²⁻, whereas Na⁺, Cl⁻ and SiO₂ concentrations showed to be controlled by dilution/concentration processes. During the 2009–2010 hydrological year, the fluxes of water, SPM and TDS registered in the snow melting–high Q season were, respectively, 71%, 92% and 67% of the annual total, whereas for equal period in 2010–2011, 56% of water, 86% of SPM and 54% of TDS annual fluxes were registered. The SPM fluxes for 2009–2010 and 2010–2011 were 1.19 × 10⁶ and 0.79 × 10⁶ t year⁻¹, whereas TDS fluxes were 0.68 × 10⁶ and 0.55 × 10⁶ t year⁻¹, respectively. Export rates for 2009–2010 were 484 t km² year⁻¹ for SPM and 275 t km² year⁻¹ for TDS. These rates are higher than those observed in glacierized granite basins and in non‐glacierized evaporite basins, suggesting a synergistic effect of lithology and glaciers on physical and chemical erosion. Copyright © 2014 John Wiley & Sons, Ltd.     

A preliminary assessment of the spatial sources of contemporary suspended sediment in the Ohio River basin,United States,using water quality data from the NASQAN programme in a source tracing procedure

Reliable information on catchment scale suspended sediment sources is required to inform the design of management strategies for helping abate the numerous environmental issues associated with enhanced sediment mobilization and off‐site loadings. Since sediment fingerprinting techniques avoid many of the logistical constraints associated with using more traditional indirect measurement methods at catchment scale, such approaches have been increasingly reported in the international literature and typically use data sets collected specifically for sediment source apportionment purposes. There remains scope for investigating the potential for using geochemical data sets assembled by routine monitoring programmes to fingerprint sediment provenance. In the United States, routine water quality samples are collected as part of the US Geological Survey's revised National Stream Quality Accounting Network programme. Accordingly, the geochemistry data generated from these samples over a 10‐year period (1996–2006) were used as the basis for a fingerprinting exercise to assess the key tributary sub‐catchment spatial sources of contemporary suspended sediment transported by the Ohio River. Uncertainty associated with the spatial source estimates was quantified using a Monte Carlo approach in conjunction with mass balance modelling. Relative frequency weighted means were used as an alternative way of summarizing the spatial source contributions, thereby avoiding the need to use confidence limits. The results should be interpreted in the context of the routine, but infrequent nature, of the suspended sediment samples used to assemble geochemistry as a basis for the sourcing exercise. Nonetheless, the study demonstrates how routine monitoring samples can be used to provide some preliminary information on sediment provenance in large drainage basins. Copyright © 2011 John Wiley & Sons, Ltd.