Factors controlling nitrogen release from two forested catchments with contrasting hydrochemical responses

Quantifying biogeochemical cycles of nitrogen (N) and the associated fluxes to surface waters remains challenging, given the need to deal with spatial and temporal variability and to characterize complex and heterogeneous landscapes. We focused our study on catchments S14 and S15 located in the Adirondack Mountains of New York, USA, which have similar topographic and hydrologic characteristics but contrasting stream nitrate ( ) concentrations. We characterized the mechanisms by which reaches the streams during hydrological events in these catchments, aiming to reconcile our field data with our conceptual model of factors that regulate nutrient exports from forested catchments. Combined hydrometric, chemical and isotopic (δ ) data showed that the relative contributions of both soil and ground water sources were similar between the two catchments. Temporal patterns of stream chemistry were markedly different between S14 and S15, however, because the water sources in the two catchments have different solute concentrations. During late summer/fall, the largest source of in S14 was till groundwater, whereas shallow soil was the largest source in S15. concentrations in surface water decreased in S14, whereas they increased in S15 because an increasing proportion of stream flow was derived from shallow soil sources. During snowmelt, the largest sources of were in the near‐surface soil in both catchments. Concentrations of increased as stream discharge increased and usually peaked before peak discharge, when shallow soil water sources made the largest contribution to stream discharge. The timing of peaks in stream concentrations was affected by antecedent moisture conditions. By elucidating the factors that affect sources and transport of N, including differences in the soil nutrient cycling and hydrological characteristics of S14 and S15, this study contributes to the overall conceptualization of release from temperate forested catchments. Copyright © 2007 John Wiley & Sons, Ltd.     

Magnesium Ammonium Phosphate Production from Wastewater through Box–Behnken Design and Its Effect on Nutrient Element Uptake in Plants

This study examined ${\rm NH}_{{\rm 4}}^{{\rm + }} $ , ${\rm PO}_{{\rm 4}}^{{\rm 3}- } $ recovery and the concentration of residual ions from anaerobic effluent of the potato processing industry through magnesium ammonium phosphate (MAP) precipitation using a Box–Behnken design. The regression model was statistically significant in terms of ${\rm NH}_{{\rm 4}}^{{\rm + }} $ and ${\rm PO}_{{\rm 4}}^{{\rm 3}- } $ removal efficiency and residual ion concentrations. Optimum ${\rm NH}_{{\rm 4}}^{{\rm + }} $ and ${\rm PO}_{{\rm 4}}^{{\rm 3}- } $ removal was obtained at pH 9.50 and at Mg²⁺/${\rm NH}_{{\rm 4}}^{{\rm + }} $ /${\rm PO}_{{\rm 4}}^{{\rm 3}- } $ molar ratio of 1.8:1:1.8. Under these conditions, Mg, Ca, K, Fe, and Cl concentrations required for plant growth significantly decreased with MAP precipitation, which was supported by EDX analysis of dry MAP precipitate. The fertilizer effect of MAP on the growth of corn and tomato plants was compared with chemical fertilizers through pot trials. Nutrient element uptake levels of plants were examined in different fertilizer sources. While Mg, Fe, Cu, Mn, and Zn nutrient element uptake levels were sufficient in MAP pots, Ca uptake exceeded sufficient level. Average levels of N, P, K, Mg, Cu, and Mn of corn plant were higher in MAP than other pots. The average N, P, and Mg levels of tomato plant in MAP pots were higher than other pots. N/K ratio, which is important in tomato plants, was better optimized in MAP pots. Only Ni, Cr, and Pb heavy metals were found in plants.     

Dynamics of Stream Water Quality during Snowmelt and Rainfall – Runoff Events in a Small Agricultural Catchment

Surface water quality can vary a lot with fluctuating discharge during a Rainfall – runoff event. This paper uses a set of hydrological and hydrochemical variables to explain concentration–discharge loops and hysteresis of ${\rm NO}_{3}^{- } $ , ${\rm NH}_{4}^{ + } $ and total suspended solids in a brook dewatering a small upland agricultural catchment in the Czech Republic. Our study is based on data collected by a continuous monitoring approach provided by an automatic ISCO sampler both from snow thawing and rainfall – runoff events. Methods of correlation, regression and principal component analysis (PCA) were employed to reveal possible relationships among the variables. For ${\rm NO}_{3}^{- } $ and ${\rm NH}_{4}^{ + } $ , we found several types of concentration–discharge loops due to the loop rotation direction and also the loop curvature shape, in mutual combinations, no matter which type of a hydrological event it was related to. PCA indicated that ${\rm NO}_{3}^{- } $ loops correlated mostly with the length of a rising hydrograph limb and with the slope of the initial phase of a falling hydrograph limb, 5‐day amount of precipitation and runoff coefficient. In case of ${\rm NH}_{4}^{ + } $ , the concentrations usually increased with elevated discharge, whereas PCA did not detect any closer linkages. For suspended solids, an unambiguous positive monotonic relationship was discovered. Although no definite pattern was found, this study showed the necessity of a continuous water quality monitoring system as an approach for capturing and understanding relationships between solute concentrations and runoff formation for tracing and modelling catchment pollution sources and describing transport processes.     

Catalytic Reduction of Hexaminecobalt(III) by Pitch‐based Spherical Activated Carbon (PBSAC)

The wet ammonia (NH₃) desulfurization process can be retrofitted to remove nitric oxide (NO) and sulfur dioxide (SO₂) simultaneously by adding soluble cobalt(II) salt into the aqueous ammonia solution. Activated carbon is used as a catalyst to regenerate hexaminecobalt(II), Co(NH₃), so that NO removal efficiency can be maintained at a high level for a long time. In this study, the catalytic performance of pitch‐based spherical activated carbon (PBSAC) in the simultaneous removal of NO and SO₂ with this wet ammonia scrubbing process has been studied systematically. Experiments have been performed in a batch stirred cell to test the catalytic characteristics of PBSAC in the catalytic reduction of hexaminecobalt(III), Co(NH₃). The experimental results show that PBSAC is a much better catalyst in the catalytic reduction of Co(NH₃) than palm shell activated carbon (PSAC). The Co(NH₃) reduction reaction rate increases with PBSAC when the PBSAC dose is below 7.5 g/L. The Co(NH₃) reduction rate increases with its initial concentration. Best Co(NH₃) conversion is gained at a pH range of 2.0–6.0. A high temperature is favorable to such reaction. The intrinsic activation energy of 51.00 kJ/mol for the Co(NH₃) reduction catalyzed by PBSAC has been obtained. The experiments manifest that the simultaneous elimination of NO and SO₂ by the hexaminecobalt solution coupled with catalytic regeneration of hexaminecobalt(II) can maintain a NO removal efficiency of 90% for a long time.     

Regulating Environmental Factors of Nutrients Release from Wheat Straw Biochar for Sustainable Agriculture

One mechanism by which biochar application enhances soil nutrient availability is through direct nutrients release from biochar. However, factors controlling the release processes are poorly understood. In this study, the effects of pH, biochar to water ratio, temperature, ionic strength, and equilibration time on the release of PO, NO, NH, K⁺, Na⁺, Ca²⁺, and Mg²⁺ from biochar were evaluated in simulated experiments. The release of PO, K⁺, Ca²⁺, and Mg²⁺ was significantly affected by extraction pH, suggesting that their release from biochar was pH dependent or an H⁺‐consuming process. Correlation analysis indicated that PO and Ca²⁺, PO and Mg²⁺, and Ca²⁺ and Mg²⁺ were co‐solubilized with increasing soil acidity. To a lesser extent, the recovery of the nutrients was also affected by the ratio of biochar to water: more nutrients were soluble with more water supply. In contrast, the release of Na was not affected by pH while the concentration increased with decreasing biochar to water ratio. Meanwhile, other factors (temperature, ionic strength, and equilibration time) had less effect on nutrient release from biochar. Under the influence of pH, the patterns of NO and PO release from biochar were different: extractable NO concentration was not affected by the pH but more PO was released in strongly acidic conditions. Our data suggested that P was mainly retained in inorganic forms while N was in organic forms in biochar. We conclude that environmental factors have marked influences on nutrients release from biochar.     

Characterizing the degree of amplitude‐variation‐with‐offset nonlinearity in seismic physical modelling reflection data

The nonlinearity of the seismic amplitude‐variation‐with‐offset response is investigated with physical modelling data. Nonlinearity in amplitude‐variation‐with‐offset becomes important in the presence of large relative changes in acoustic and elastic medium properties. A procedure for pre‐processing physical modelling reflection data is enacted on the reflection from a water‐plexiglas boundary. The resulting picked and processed amplitudes are compared with the exact solutions of the plane‐wave Zoeppritz equations, as well as approximations that are first, second, and third order in , , and . In the low angle range of 0°–20°, the third‐order plane‐wave approximation is sufficient to capture the nonlinearity of the amplitude‐variation‐with‐offset response of a liquid‐solid boundary with , , and ρ contrasts of 1485–2745 m/s, 0–1380 m/s, and 1.00–1.19 gm/cc respectively, to an accuracy value of roughly 1%. This is in contrast to the linear Aki–Richards approximation, which is in error by as much as 25% in the same angle range. Even‐order nonlinear corrective terms are observed to be primarily involved in correcting the angle dependence of , whereas the odd‐order nonlinear terms are involved in determining the absolute amplitude‐variation‐with‐offset magnitudes.     

Photocatalytic Degradation of 17α‐Ethinylestradiol and Inactivation of Escherichia coli Using Ag‐Modified TiO2 Nanotube Arrays

Ag‐modified TiO₂ nanotube arrays (Ag/TiO₂ NAs) were prepared and employed as a photocatalyst for degradation of 17α‐ethinylestradiol (EE2) and inactivation of Escherichia coli. The as‐synthesized Ag/TiO₂ NAs were characterized by field‐emission scanning electron microscope (FESEM), X‐ray diffraction (XRD), and X‐ray photoelectron spectroscopy (XPS). It was found that metallic Ag nanoparticles were firmly deposited on the TiO₂ NAs with the pore diameter of 100 nm and the length of 550 nm. Photocatalytic degradation of EE2 and inactivation of E. coli were enhanced effectively in an analogical trend using Ag/TiO₂ NAs. In particular, Ag/TiO₂ NAs exhibited the antimicrobial activity even in the absence of light. The Ag acted as a disinfection agent as well as the dopant of the modified TiO₂ NAs photocatalysis by forming a Schottky barrier on the surface of TiO₂ NAs. Inorganic ions suppressed the rates of photocatalytic degradation of EE2, with HCO having a more pronounced effect than NO or SO. Humic acid (HA) was found to increase the rate of EE2 degradation.     

Diel patterns in coastal‐stream nitrate concentrations linked to evapotranspiration in the riparian zone of a low‐relief,agricultural catchment

Evapotranspiration (ET) can cause diel fluctuations in the elevation of the water table and the stage in adjacent streams. The diel fluctuations of water levels change head gradients throughout the day, causing specific discharge through near‐stream sediment to fluctuate at the same time scale. In a previous study, we showed that specific discharge controls the residence time of groundwater in streambed sediment that, in turn, exerted the primary control on removal from groundwater passing through the streambed. In this study, we examine the magnitude of diel specific discharge patterns through the streambed driven by ET in the riparian zone with a transient numerical saturated–unsaturated groundwater flow model. On the basis of a first‐order kinetic model for removal, we predicted diel fluctuations in stream concentrations. Model results indicated that ET drove a diel pattern in specific discharge through the streambed and riparian zone (the removal zones). Because specific discharge is inversely proportional to groundwater travel time through the removal zones and travel time determines the extent of removal, diel changes in ET can result in a diel pattern in concentration in the stream. The model predictions generally matched observations made during summertime base‐flow conditions in a small coastal plain stream in Virginia. A more complicated pattern was observed following a seasonal drawdown period, where source components to the stream changed during the receding limb of the hydrograph and resulted in diel fluctuations being superimposed over a multi‐day trend in concentrations. Copyright © 2013 John Wiley & Sons, Ltd.     

Stream response to precipitation variability: a spectral view based on analysis and modelling of hydrological cycle components

Hydrological processes commonly exhibit long‐term persistence, also known as the ‘Hurst phenomenon’. Here, we examine long‐term precipitation and streamflow time series from the Elbe River Basin to quantify differences in the spectral properties and in the Hurst parameter estimates () of the individual hydrological cycle components. Precipitation‐runoff modelling is performed for the Elbe River sub‐catchment Striegis using the Soil and Water Assessment Tool (SWAT). For 38 daily 50 years long streamflow time series from the Elbe River Basin, baseflow separation and spectral analysis is performed. The results show a spectral shift towards low‐frequency scales (>2 years) from precipitation to baseflow, with a parallel increase of from 0.52 (precipitation) to 0.65 (baseflow). The SWAT model is able to reproduce both, the main low‐frequency mode (≈7 yr.) and the (0.62) of the observed Striegis River flow time series. The baseflow appears to be the main component which shapes the low‐frequency response and of streamflow in the Elbe River Basin to the input precipitation. This conclusion is further confirmed through PMWIN‐MODFLOW groundwater modelling of a hypothetic phreatic stream‐connected aquifer system that consists of various soils (sand, loamy sand and silt). A power shift towards lower frequencies and an increase of for the hydraulic heads is obtained, as the aquifer's lateral dimensions increase and its hydraulic conductivity decreases. The average of the groundwater heads is 0.80, 0.90 and 1.0 for sand, loamy sand and silt aquifers, respectively. Copyright © 2014 John Wiley & Sons, Ltd.     

Adsorption of Complex Pollutants from Aqueous Solutions by Nanocomposite Materials

In view of water pollutants becoming more complex, both anionic and cationic pollutants need to be removed. The multi‐pollutants simultaneous removal is paid more and more attention. Hence, development composite materials for treatment complex wastewater are the aim of this study. In this research, iron–nickel nanoparticles deposited onto aluminum oxide (α‐Al₂O₃) and carbon nanotubes (CNTs) to form nanocomposite materials Fe–Ni/Al₂O₃ and Fe–Ni/CNTs, respectively, were used as adsorbents. The adsorption capacities of Fe–Ni/Al₂O₃ and Fe–Ni/CNTs for AO7, HSeO, and Pb²⁺ were observed to be 5.46, 8.28, 27.02, and 25.6 mg/g, 15.29 and 17.12 mg/g, separately. The composite materials with negative charges were superior in adsorption of anionic pollutants. Using orthogonal experimental design and analysis of variance to co‐treat dye AO7, HSeO and Pb²⁺ in aqueous solutions, seven testing factors were included: (1) adsorbent types, (2) amount of iron, (3) solution pHs, (4) AO7 concentrations, (5) Pb²⁺ concentrations, (6) HSeO concentrations and (7) reaction time. The experimental results showed that the removal of complex pollutants AO7, HSeO, and Pb²⁺ on Fe–Ni/CNTs could reach up to 90% in the optimal treatment conditions. When using Fe–Ni/CNTs as the adsorbent, the sorption isothermals were well fitted in the Freundlich isotherm, and R² could reach up to 0.98.     

Using Chlorine Dioxide to Remove the Fouling of Ultrafiltration Membrane and Control Disinfection By‐Products

Ultrafiltration (UF) can remove natural organic matter (NOM) effectively. Moreover, chlorine dioxide (ClO₂) has been an alternative disinfectant as it forms fewer disinfection by‐products with NOM than chlorination does. Therefore, combining ClO₂ with UF may improve conventional purification processes. In this study, feed water containing humic acid with 4.07 mg/L total organic carbon (TOC) was dosed directly with various amounts of ClO₂ (0, 2, 5, 10, and 15 mg/L) before being filtered through a 5‐kDa UF membrane. With a low dose (2 mg/L ClO₂), UF removed humic acid effectively, as TOC was not detected in the permeate, and the permeate flux increased to about 80% of the initial permeate flux by cross flow. Moreover, the concentrations of ClO, ClO, and trihalomethanes in the permeate were below the United States Environmental Protection Agency guidelines.     

The influence of fire and permafrost on sub‐arctic stream chemistry during storms

Permafrost and fire are important regulators of hydrochemistry and landscape structure in the discontinuous permafrost region of interior Alaska. We examined the influence of permafrost and a prescribed burn on concentrations of dissolved organic carbon (DOC), dissolved organic nitrogen (DON) and other solutes ( , Ca²⁺, K⁺, Mg²⁺, Na⁺) in streams of an experimentally burned watershed and two reference watersheds with varying extents of permafrost in the Caribou–Poker Creeks Research Watershed in interior Alaska. The low‐permafrost watershed has limited permafrost (3%), the high‐permafrost watershed has extensive permafrost (53%), and the burn watershed has intermediate permafrost coverage (18%). A three end‐member mixing model revealed fundamental hydrologic and chemical differences between watersheds due to the presence of permafrost. Stormflow in the low‐permafrost watershed was dominated by precipitation and overland flow, whereas the high‐permafrost watershed was dominated by flow through the active layer. In all watersheds, organic and groundwater flow paths controlled stream chemistry: DOC and DON increased with discharge (organic source) and base cations and (from weathering processes) decreased. Thawing of the active layer increased soil water storage in the high‐permafrost watershed from July to September, and attenuated the hydrologic response and solute flux to the stream. The FROSTFIRE prescribed burn, initiated on 8 July 1999, elevated nitrate concentrations for a short period after the first post‐fire storm on 25 July, but there was no increase after a second storm in September. During the July storm, nitrate export lagged behind the storm discharge peak, indicating a flushing of soluble nitrate that likely originated from burned soils. Copyright © 2006 John Wiley & Sons, Ltd.     

Time‐lapse pre‐stack seismic data registration and inversion for CO2 sequestration study at Cranfield

Pre‐stack seismic data are indicative of subsurface elastic properties within the amplitude versus offset characteristic and can be used to detect elastic rock property changes caused by injection. We perform time‐lapse pre‐stack 3‐D seismic data analysis for monitoring sequestration at Cranfield. The time‐lapse amplitude differences of Cranfield datasets are found entangled with time‐shifts. To disentangle these two characters, we apply a local‐correlation‐based warping method to register the time‐lapse pre‐stack datasets, which can effectively separate the time‐shift from the time‐lapse seismic amplitude difference without changing the original amplitudes. We demonstrate the effectiveness of our registration method by evaluating the inverted elastic properties. These inverted time‐lapse elastic properties can be reliably used for monitoring plumes.     

Spatial and temporal variations in rainfall characteristics in mountainous and lowland areas in Taiwan

Although changes in rainfall characteristics have been noted across the world, few studies have reported those in mountainous areas. This study was undertaken to clarify spatial and temporal variations in rainfall characteristics such as annual rainfall amount (Pr), mean daily rainfall intensity (η), and ratio of rain days (λ) in mountainous and lowland areas in Taiwan. To this aim, we examined spatial and year‐to‐year variations and marginal long‐term trends in Pr, η, and λ, based on rainfall data from 120 stations during the period 1978–2008. The period mean rainfall () at the lowland stations had strong relationships with the period mean daily rainfall intensity () and the period mean ratio of rain days () during those 31 years. Meanwhile, was only strongly related to at mountainous stations, indicating that influences on spatial variations in were different between lowland and mountainous stations. Year‐to‐year variations in Pr at each station were primarily determined from the variation in η at most stations for both lowland and mountainous stations. Long‐term trend analysis showed that Pr and η increased significantly at 10% and 31% of the total 120 stations, respectively, and λ decreased significantly at 6% of the total. The increases in Pr were mostly accompanied by increases in η. Although stations with significant η increases were slightly biased toward the western lowland area, increases or decreases in Pr and λ were not common. These results contribute to understanding the impacts of possible climate changes on terrestrial hydrological cycles. Copyright © 2012 John Wiley & Sons, Ltd.     

Removal of Ni(II) from Aqueous Solutions by Nanoscale Magnetite

Magnetite nanoparticles were applied to remove Ni(II) from aqueous solutions as a function of pH, contact time, supporting electrolyte concentration, and analytical initial Ni(II) concentration. The highly crystalline nature of the magnetite structure with diameter of around 10 nm was characterized with transmission electron microscopy (TEM) and X‐ray diffractometry (XRD). The surface area was determined to be 115.3 m²/g. Surface chemical properties of magnetite at 25°C in aqueous suspensions were investigated. The point of zero charge (pHzpc) was found to be 7.33 and the intrinsic acidity constants (${\rm p}K_{{\rm a}1}^{{\rm s}} $ and ${\rm p}K_{{\rm a}2}^{{\rm s}} $ ) were found to be 9.3 and 5.9, respectively. The surface functional groups were investigated with Fourier transform‐infrared spectroscopy (FTIR) as well. Batch experiments were carried out to determine the adsorption kinetics and mechanism of Ni(II) by these magnetite nanoparticles. The adsorption process was found to be pH dependent. In NaCl solutions, Ni(II) adsorption increased with increasing ionic strength while in NaClO₄ solutions, Ni(II) adsorption exhibited little dependence on the ionic strength of the solution. The adsorption process better followed the pseudo‐second order equation and Freundlich isotherm.     

Temporal and spatial behaviour of rip channels in a multiple‐barred coastal system

A 15‐month data set of daily time‐averaged video images (Argus) has been analyzed to describe the spatial and temporal variability of the rip channels on a multiple‐barred coast at Noordwijk aan Zee, The Netherlands. The landward boundary of the intertidal bars and a proxy of the subtidal bar crest, defined as the intertidal and subtidal bar lines respectively, were derived from the Argus images. Local seaward‐directed deviations of the bar lines represent the cross‐shore and alongshore locations of the rip channels. The average intertidal rip spacing ( ) was 243 m, but the rips were not spaced regularly (σ_λ/ = 0.47). Some intertidal rips were observed to fill up during falling tide, but the majority remained open. The filled intertidal rip channels had more landward positions and migrated more slowly (2.4 versus 4.6 m/day) in the alongshore direction than the open intertidal rip channels. The number and the alongshore migration rate of open intertidal rip channels increased with the preceding wave heights (r = 0.26, p < 0.01) and alongshore component of the offshore wave power (r = 0.25, p < 0.01), respectively. The shape of the intertidal bar lines was similar to the subtidal bar line shape, suggesting that the intertidal morphology is coupled to the subtidal alongshore variability. The phase of two bar lines could vary from in phase (0°) to out of phase (180°). The phase changes gradually, due to different alongshore migration rates of the intertidal and subtidal bar lines. Copyright © 2009 John Wiley & Sons, Ltd.     

Characterization and Application of Dried Plants to Remove Heavy Metals,Nitrate, and Phosphate Ions from Industrial Wastewaters

Low cost adsorbents were prepared from dried plants for the removal of heavy metals, nitrate, and phosphate ions from industrial wastewaters. The efficiency of these adsorbents was investigated using batch adsorption technique at room temperature. The dried plant particles were characterized by N₂ at 77 K adsorption, scanning electron microscopy, energy dispersive X‐ray spectroscopy, Fourier transform infrared spectroscopy, and phytochemical screening. The adsorption experiments showed that the microparticles of the dried plants presented a good adsorption of heavy metals, phosphate, and nitrate ions from real wastewaters. This adsorption increased with increasing contact time. The equilibrium time was found to be 30 min for heavy metals and nitrate ions and 240 min for phosphate ions. After the adsorption process, the Pb(II) concentrations, as well as those of Cd(II), Cu(II), and Zn(II) were below the European drinking water norms concentrations. The percentage removal of heavy metals, nitrates, and phosphates from industrial wastewaters by dried plants was ～94% for Cd²⁺, ～92% for Cu²⁺, ～99% for Pb²⁺, ～97% for Zn²⁺, ～100% for ${\rm NO}_{{\rm 3}}^{{-} } $ and ～77% for ${\rm PO}_{{\rm 4}}^{3{-} } $ ions. It is proved that dried plants can be one alternative source for low cost absorbents to remove heavy metals, nitrate, and phosphate ions from municipal and industrial wastewaters.     

Effect of SO on 1,1,1‐Trichloroethane Degradation by Fe0 in Aqueous Solution

Sulfate in groundwater has been previously shown to change the reactivity of Fe⁰ in permeable reactive barriers for reducing chlorinated organics. To better understand the effect and mechanism of SO, the degradation of 1,1,1‐trichloroethane (TCA) by Fe⁰ in unbuffered aqueous solutions with and without SO was investigated. In a Fe⁰‐TCA‐H₂O system with initial pH of 2.0 to 10.0, the maximum removal rate of TCA was achieved at the initial pH 6.0 with pseudo‐first‐order constant K_obs 9.0 × 10^?3/min. But in a Fe⁰‐TCA‐Na₂SO₄‐H₂O system, the removal rate of TCA decreased remarkably with a reduction in K_obs to 1.0 × 10^?3/min, and the pH varied from 6.0 to 9.6, indicating an inhibition of TCA dehydrochlorination by SO. Sulfate remarkably inhibited TCA degradation via changing the route of Fe⁰ dissolution. It accelerated the dissolution of Fe⁰ and transformed the intermediate form Fe(OH)_ads to Fe₂(SO₄)_ads, which weakened the affinity between Fe and TCA, and thus depressed the degradation of TCA by Fe⁰.     

Spectral decomposition and de‐noising via time‐frequency and space‐wavenumber reassignment

The reassignment method remaps the energy of each point in a time‐frequency spectrum to a new coordinate that is closer to the actual time‐frequency location. Two applications of the reassignment method are developed in this paper. We first describe time‐frequency reassignment as a tool for spectral decomposition. The reassignment method helps to generate more clear frequency slices of layers and therefore, it facilitates the interpretation of thin layers. The second application is to seismic data de‐noising. Through thresholding in the reassigned domain rather than in the Gabor domain, random noise is more easily attenuated since seismic events are more compactly represented with a relatively larger energy than the noise. A reconstruction process that permits the recovery of seismic data from a reassigned time‐frequency spectrum is developed. Two approaches of the reassignment method are used in this paper, one of which is referred to as the trace by trace time reassignment that is mainly used for seismic spectral decomposition and another that is the spatial reassignment that is mainly used for seismic de‐noising. Synthetic examples and two field data examples are used to test the proposed method. For comparison, the Gabor transform method, inversion‐based method and common deconvolution method are also used in the examples.     

Research Note: Experimental measurements of Q‐contrast reflections

While seismic reflection amplitudes are generally determined by real acoustical impedance contrasts, there has been recent interest in reflections due to contrasts in seismic‐Q. Herein we compare theoretical and modelled seismic reflection amplitudes for two different cases of material contrasts. In case A, we examine reflections from material interfaces that have a large contrast in real‐valued impedance () with virtually no contrast in seismic‐Q. In case B, we examine reflections from material interfaces that have virtually no contrast in but that have very large seismic‐Q contrasts. The complex‐valued reflection coefficient formula predicts non‐zero seismic reflection amplitudes for both cases. We choose physical materials that typify the physics of both case A and case B. Physical modelling experiments show significantly large reflections for both cases – with the reflections in the two cases being phase shifted with respect to each other, as predicted theoretically. While these modelling experiments show the existence of reflections that are predicted by theory, there are still intriguing questions regarding the size of the Q‐contrast reflections, the existence of large Q‐contrast reflections in reservoir rocks and the possible application of Q‐reflection analysis to viscosity estimation in heavy oilfields.