Separation of Vanillin from Oil Palm Empty Fruit Bunch Lignin

The separation of vanillin from the lignin of empty fruit bunch oil palm is presented in this study. The lignin was extracted from soda black liquor derived from oil palm empty fruit bunches (EFB) using 20% sulfuric acid. Nitrobenzene oxidation was carried out by adding 50 mg of dry EFB lignin into a mixture of 7 mL of 2 M NaOH and 4 mL of nitrobenzene in a 15 mL steel autoclave. The autoclave was sealed tightly with a screw cap fitted with a Teflon gasket and heated to 165°C for 3 h in a preheated thermostatic oil bath. High performance liquid chromatography (HPLC) was used to determine the concentration of each compound present in the lignin. There were eight compounds detected in the HPLC chromatogram. The crystallization process was then used as a method to separate vanillin from other compounds. Based on the solubility of vanillin in acetone, 15 mL of acetone was added to the residue of the oxidized products and heated to 60°C for 10 min. A yield of 1.6% vanillin was isolated from a 50 mg lignin sample. The isolated compound was analyzed with HPLC, Fourier transform infrared spectrophotometry (FT‐IR) and nuclear magnetic resonance (¹³C‐NMR) for structural verification. The results of the characterization studies proved that the isolated compound is vanillin.     

Natural and experimental structural evolution of dispersed organic matter in mudstones: The Shimanto accretionary complex,southwest Japan

Structural changes induced by thermal maturation of dispersed organic matter (OM) in the Shimanto accretionary complex, southwest Japan, were investigated using micro‐Fourier‐transform infrared spectroscopy and micro‐Raman spectroscopy. Natural dispersed OM exhibits systematic structural changes inferred from D1‐ and G‐band FWHM values, Raman band separation (RBS), and intensity ratios of the D1‐ and G‐bands (I_D1/I_G ratio) from diagenetic zone to anchizone (IC values: 0.75–0.30). Infrared spectra indicate a loss of aliphatic CH _x, aromatic CH _x, and oxygen‐containing structures as temperature increases. These changes are consistent with discontinuities in thermal structures bounded by out‐of‐sequence thrusts. Kinetic pyrolysis experiments indicate that the I_D1/I_G ratio of synthesized OM has a power law relationship with heat treatment time. Kinetic models of temperature dependence were fitted using the I_D1/I_G ratio, and an effective activation energy of 106 ±17 kJ/mol was estimated using an Arrhenius equation. The activation energies estimated by power law rate and Avrami models have a least‐square correlation coefficient of 0.93, indicating the temperature dependence of carbonization. The estimated effective activation energy is consistent with that of coal, lignin, cellulose, and hemicellulose during thermal degradation. On the other hand, RBS, and D1‐ and G‐band FWHM values of OM display more complex changes with increasing heating temperature and time, and it is difficult to constrain rate parameters during pyrolysis experiments. Our data indicate that the I_D1/I_G ratio is controlled by a simple thermally activated process, whereas RBS and D1‐ and G‐band FWHM values can be affected by lithostatic pressure, fluid activity, hydrogen index, and host lithology, as well as temperature. Structural evolution of dispersed OM in mudstones differs between natural and anhydrous closed experimental systems. Natural carbonization based on micro‐Raman spectroscopy should be applied for a limited indicator of thermal maturation, especially for dispersed OM in diagenetic zone.     

Assessment of Cyto‐ and Genotoxic Effects of a Variety of Chemicals Using Saccharomyces cerevisiae

Saccharomyces cerevisiae as the most simple eukaryotic organism is broadly accepted as a laboratory model organism. For the detection of potential toxic effects of pure compounds and complex composed samples like wastewater a miniaturised short‐term in vitro cyto‐ and genotoxicity screening assay was developed. The assay based on genetically modified S. cerevisiae cells deleted in the prominent drug efflux transporters Pdr5, Snq2, and Yor1 that facilitate pleiotropic drug resistance. The yeast strain devoid of these proteins that mediate the efflux of structurally diverse hydrophobic compounds exhibited an increased sensitivity to a variety of organic compounds. The DNA damage inducible RAD54 promoter fused to a yeast optimized derivative of the GFP (green fluorescent protein) gene from the jelly fish Aequorea victoria served as an indicator of DNA damage in this strain. Various pure compounds including the direct‐acting genotoxins methyl‐N‐nitro‐N‐nitrosoguanidine (MNNG), 4‐nitroquinoline‐N‐oxide (4‐NQO), methyl methanesulfonate (MMS) and hydroxyurea as well as the heavy metals cadmium and chromium(VI), the insecticide lindane and the central nervous system stimulant caffeine were tested exhibiting dose dependent induction of green fluorescence. All compounds were in parallel examined for chronic toxicity. A bioassay detecting simultaneously geno‐ and cytotoxic effects of potential toxicants in a single assay can be an important tool with a variety of applications in environmental monitoring and aquatic ecotoxicology. By partial automation and miniaturisation to microtitration scale this bioassay enables sensitive and fast biomonitoring for a multitude of samples.     

Rock physics analysis for time-lapse seismic at Schiehallion Field, North Sea

Rock physics analysis plays a vital role in time‐lapse seismic interpretation because it provides the link between changes in rock and fluid properties and the resulting seismic data response. In this case study of the Schiehallion Field, we discuss a number of issues that commonly arise in rock physics analyses for time‐lapse studies. We show that:

• 1 Logarithmic fits of dry bulk (K_dry) and shear (G_dry) moduli vs. effective pressure (P_eff) are superior to polynomial fits.
• 2 2D surface fits of K_dry and G_dry over porosity (φ) and effective pressure using all the core data simultaneously are more useful and accurate than separate 1D fits over φ and P_eff for each individual core.
• 3 One average set (facies) of K_dry(φ, P_eff) and G_dry(φ, P_eff) can be chosen to represent adequately the entire Schiehallion reservoir.
• 4 Saturated velocities and densities modelled by fluid substitution of K_dry(φ, P_eff), G_dry(φ, P_eff) and the dry bulk density ρ_dry(φ) compare favourably with well‐log velocities and densities.
• 5 P‐ and S‐wave impedance values resulting from fluid substitution of K_dry(φ, P_eff), G_dry(φ, P_eff) and ρ_dry(φ) show that the largest impedance changes occur for high porosities and low effective pressures.
• 6 Uncertainties in K_dry(φ, P_eff) and G_dry(φ, P_eff) derived for individual cores can be used to generate error surfaces for these moduli that represent bounds for quantifying uncertainties in seismic modelling or pressure–saturation inversion.

     

Exchangeable Characteristics of Potassium in Five Important Soils of Taiwan

The application of potassium fertilizer by farmers is often not appropriate and causing environmental pollution. By understanding the adsorptive characteristics of potassium (K) on different soils, we can prevent excessive application of K‐fertilizer that can cause environmental impact. The Gapon exchange coefficient (K_G), for exchange between K and Ca, was considered as an important factor influencing the adsorption of K. This study was conducted to compare the constant K_G of five important farm soils in Taiwan. The K_G and CEC were then used to predict K buffering capacity (PBC). Finally, the relationship between exchangeable K ratio (E_P) and K adsorption ratio (PAR) was examined. The results show that five soils have same trends, indicating that K_G decreases with increase in K saturation. The CEC and K_G of Liuying (Ly) soil are both high, so that their K buffering capacity is high. The K_G and CEC of Chanjing (Cj) and Sanhua (Sh) soil show moderate values. The CEC of Erling (El) soil is high, but its K_G is low, so that its K buffering capacity is moderate. On the other hand, the K_G of Newniaokang (Nnk) soil is high but its CEC is low, so its K buffering capacity is also moderate. The correlations between E_P and PAR of five soil show linear relationship at three treatments of CaCl₂ concentration. This study may provide an important clue to the fertilization management of K‐fertilizer on the different soil properties in Taiwan.     

Field Treatment of MTBE‐Contaminated Groundwater Using Ozone/UV Oxidation

Methyl‐tertiary butyl ether (MTBE) is often found in groundwater as a result of gasoline spills and leaking underground storage tanks. An extrapolation of occurrence data in 2008 estimated at least one detection of MTBE in approximately 165 small and large public water systems serving 896,000 people nationally (United States Environmental Protection Agency [U.S. EPA] 2008). The objective of this collaborative field study was to evaluate a small groundwater treatment system to determine the effectiveness of ultraviolet (UV)/ozone treatment in removing MTBE from contaminated drinking water wells. A pilot‐scale advanced oxidation process (AOP) system was tested to evaluate the oxidation efficiency of MTBE and intermediates under field conditions. This system used ozone as an oxidizer in the presence of UV light at hydraulic retention times varying from 1 to 3 min. MTBE removal efficiencies approaching 97% were possible with this system, even with low retention times. The intermediate t‐butyl alcohol (TBA) was removed to a lesser extent (71%) under the same test conditions. The main intermediate formed in the oxidation process of the contaminated groundwater in these studies was acetone. The concentrations of the other anticipated intermediates t‐butyl formate (TBF), isopropyl alcohol (IPA), methyl acetate (MAc), and possible co‐occurring aromatics (BTEX) in the effluent were negligible.     

S‐Doped Magnetic Mesoporous Carbon for Efficient Adsorption of Methyl Orange from Aqueous Solution

A simple and rapid soft‐templating coupled with one‐pot solvent thermal method is developed to synthesize S‐doped magnetic mesoporous carbon (S‐doped MMC). In this method, phenolic resin is used as a carbon precursor and Pluronic copolymer P123 is used as a template and 2,5‐dimercapto‐1,3,4‐thiadiazole is used as sulfur source. Prepared S‐doped MMC processes a high specific surface area, the Fe₃O₄ particles are well embedded in the mesoporous carbon walls that exhibit a strong magnetic response, and the hydrated iron nitrate loading amount of 0.808 g is the best. Batch adsorption experiments are carried out at different pH, initial concentration, temperature, and contact time on the adsorption of methyl orange (MO) by S‐doped MMC. The kinetic data of the adsorption process are better fitted with pseudo‐second‐order model than the pseudo‐first‐order model. Langmuir model is more suitable for the equilibrium data than Freundlich model. The thermodynamic parameters including ΔG⁰, ΔH⁰, and ΔS⁰ indicate that the adsorption is a feasible, spontaneous, and endothermic process. Finally, it is found that the coexistence of PO₄^3?, NO₃^?, SO₄^2?, Cl^?, and CO₃^2? does not influence the adsorption process. These results illustrate S‐doped MMC can be an efficient adsorbent for the removal of MO from wastewater.     

Adsorption Performance and Mechanism in Binding of Azo Dye by Raw Bentonite

The adsorption behavior of methyl orange (MO) from aqueous solution onto raw bentonite (RB) sample was investigated as a function of parameters such as pH, inorganic anion, contact time, and temperature. The Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherms. Langmuir adsorption capacity was found to be 34.34 mg/g at pH 4.0. The pseudo‐first‐order, pseudo‐second‐order kinetic, and the intra‐particle diffusion models were used to describe the kinetic data. The values of the energy (E_a), enthalpy (ΔH^≠), and entropy of activation (ΔS^≠) were calculated as 38.62 kJ/mol, 36.04 kJ/mol, and ?150.05 J/mol K, respectively, at pH 4.0.     

Quantitation of Nonextractable Anthropogenic Quantitation of Nonextractable Anthropogenic Sediments after Chemical Degradation

Four highly contaminated sediment samples obtained from three sampling locations of the Teltow Canal, Berlin, were investigated by quantitation of extractable and nonextractable organic contaminants. The selection of the anthropogenic contaminants (including chlorinated and brominated naphthalenes, 2, 4, 6‐tribromoaniline, phthalates, tri‐n‐butylphosphate, 2, 2, 4‐trimethyl‐1, 3‐pentanediol diisobutyrate, bisphenol A, butylated nitrophenols, 4‐nitrobenzoic acid, galaxolide, and tonalide) based on the results of extended GC‐MS screening analyses applied to the extracts of the sediment samples as well as to the extracts derived from selective chemical degradation procedures. In detail, alkaline hydrolyses, BBr₃‐treatment and RuO₄‐oxidation were applied to the pre‐extracted sediment samples in both a separate and a sequential mode.     

太湖沉积物中长链脂肪酸甲酯化合物的检出及意义

在太湖表层沉积物中检测出丰度较高的一系列长链脂肪酸甲酯化合物,采用标准图谱与质谱解析相结合的方法进行鉴定,长链脂肪酸甲酯化合物有类似正构烷烃的分布型式,碳数分布范围为Ｃ１４－Ｃ３４,主峰碳为Ｃ１６,具有明显的偶碳优势。     

Measurement of evapotranspiration in a winter wheat field

Daily evapotranspiration from a winter wheat field on the North China Plain measured by large‐scale weighing lysimeter was linearly related to that measured by the Bowen ratio energy balance (BREB) technique. Soil evaporation averaged about 23·6% of evapotranspiration from the post‐winter dormancy revival stage to the grain ripening stage in 1999. On clear days during winter dormancy, about half of the net radiation flux R_n was used to warm soil. During the revival stage, conductive heat flux G also used most of the incoming R_n, but the ratio of latent heat flux λE to R_n increased. During the stem‐extension stage, λE was about 50% of R_n; thereafter, λE/R_n increased continually, but G remained less than 10% of R_n. During the ripening stage, λE was almost 90% of R_n. Evaporative fraction (EF) can be expressed as a function of plant status and atmospheric boundary layer conditions. The relationship between EF and available energy under moderate air temperature and vapour pressure deficit conditions was examined for five combinations of aerodynamic and canopy conductance. Although the theoretical relationship indicates that EF should be highly correlated to soil water content, the correlation has been difficult to identify under field conditions. However, we observed that there exists a threshold value of R_n ? G, above which EF is less than 1·0, and that the threshold value is lower under soil‐water deficit conditions than under abundant soil‐water conditions. Copyright © 2002 John Wiley & Sons, Ltd.     

Sorption Behaviour of Phenols on Natural Sandy Aquifer Material during Flow‐through Column Experiments: The Effect of pH

Flow‐through column experiments were carried out to investigate the influence of pH on the sorption of three phenols (2‐methyl‐4, 6‐dinitrophenol, 2, 4, 6‐trichlorophenol, pentachlorophenol) onto a natural sandy aquifer material collected from a bank filtration site of River Elbe, Germany. For the phenols investigated, an increase in sorption (retardation) with decreasing pH is observed indicating a stronger sorption of the neutral species in comparison to that of the anions formed by dissociation. The anions of 2‐methyl‐4, 6‐dinitrophenol and 2, 4, 6‐trichlorophenol do not show significant sorption. On the contrary, pentachlorophenol showed sorption not only in neutral form but also in ionic form significantly which should be taken into account while assessing the fate and transport of such compound. A linear model based on the degree of protonation (calculated from pH and pK_a) can be used to resolve the apparent (observed) sorption coefficient (K_{d, app}) into its neutral (K_{d, n}) and ionised (K_{d, i}) components. Knowing pK_a, K_{d, n}, and K_{d, i} the apparent sorption coefficient for pH values other than experimentally investigated can be predicted.     

Use of the Acoustic Energy Meter (AEM) for rapid geomorphological field assessment of rock hardness: comparison with Schmidt hammer R‐value

Rapid, field‐based assessments of rock hardness are required in a broad range of geomorphological investigations where rock intact strength is important. Several different methods are now available for taking such measurements, in particular the Schmidt hammer, which has seen increasing use in geomorphology in recent decades. This is despite caution from within the engineering literature regarding choice of Schmidt hammer type, normalization of rebound (R‐) values, surface micro‐roughness, weathering degree and moisture content, and data reduction/analysis procedures. We present a pilot study of the use of an Acoustic Energy Meter (AEM), originally produced, tested and developed within the field of underground mining engineering as a rapid measure of rock surface hardness, and compare it with results from a mechanical N‐Type Schmidt hammer. We assess its capabilities across six lithological study sites in southeast Queensland, Australia, in the Greater Brisbane area. Each rock exposure has been recently exposed in the 20th/21st century. Using a ‘paired’ sampling approach, the AEM G‐value shows an inverse relationship with Schmidt hammer R‐value. While both devices show variability with lithology, the AEM G‐values show less scatter than the Schmidt hammer. We conclude that each device can contribute to useful rock hardness testing in geomorphological research, but the AEM requires further field testing in a range of environments, and in particular on older and naturally‐exposed rock surfaces. Future evaluations can extend this pilot study by focusing on sampling procedures, energy sources, and data reduction protocols, within the framework of a comparison study with other rock hardness testing apparatus. Copyright © 2016 John Wiley & Sons, Ltd.     

Treatment of a Trifluraline Effluent by Means of Oxidation‐Coagulation with Fe(VI) and Combined Fenton Processes

The amination water (AW) effluent stream from the industrial production of the trifluraline herbicide was submitted to an oxidation‐coagulation treatment with potassium ferrate, combined with advanced oxidation processes. The experimental results obtained by analysis of variance (ANOVA) for the oxidation‐coagulation‐Fenton process, evaluating the variables pH (A), Fe(VI) concentration (B), and H₂O₂ concentration (C), demonstrated that the regression equation resulting from the Response Surface Methodology (RSM) experimental design, for the quadratic model, was η_Abs (%) = 36.9– 21.58A + 8.37A² + 1.36B + 0.92B² + 1.08C + 1.52C² + 1.27AB – 1.34AC + 1.33BC. The maximum absorptiometric color reduction occurred at pH 3, with corresponding maximum amounts of iron and hydrogen peroxide. The absorptiometric color and COD reduction were 96% and 57%, respectively. For the oxidation‐coagulation‐photo‐Fenton process, the analyzed variables were pH (A), Fe(VI) concentration (B), H₂O₂ concentration (C), and temperature (D). The regression equation resulting from the quadratic model was η_Abs (%) = 38.3 – 20.2A + 8.12A² – 0.27B + 3.73B² + 0.3C + 3.6C² + 1.67D + 3.1D² + 1.72AB + 0.51AC – 1.82AD + 0.74BC – 1.11BD + 0.03CD. The ANOVA response showed that the highest absorptiometric color reduction occurred at pH 3, with respective maximum amounts of iron and hydrogen peroxide at 60°C. The maximum efficiencies achieved by the proposed treatment process for the trifluraline effluent stream were 95% and 85%, for absorptiometric color and COD reduction, respectively.     

Development and Characterization of Lignin‐Based Hydrogel for Use in Agricultural Soils: Preliminary Evidence

In arid and semi‐arid regions of the world, agricultural production is greatly limited by water scarcity and inefficient water use. Water‐absorbent hydrogels are a technological solution that can retain soil water for plants. A lignin‐based hydrogel as a natural plant‐based water absorbent is prepared from lignin alkali polymers and poly(ethylene glycol) diglycidyl ether (PEGDGE) in adjusted alkali (NaOH) solution. The maximum swelling capacity of the hydrogel is achieved in 1.5 m NaOH with 0.5 mmol PEGDGE g ${}_{\mathrm{lignin}}^{?1}$. Water swelling capacity is 34 g g ${}_{\mathrm{Hydrogel}}^{?1}$ dry weight of hydrogel in distilled water, which is reduced to 53% and 64% in 0.1 m NaCl and 0.1 m CaCl₂ solution, respectively. Biodegradability and phytotoxicity tests show that 6.5% of the sample mass decomposed after 40 days of incubation in soil solution media and the hydrogel is not phytotoxic to wheat seeds. These findings support the use of the lignin‐based hydrogel as an environmentally friendly additive to promote water retention in dry, saline soils. Due to the limitations of this study, further assessments are needed in order to understand the efficiency of lignin‐based hydrogel application in different soils with different biota.     

Investigation of Arsenotrophic Microbiome in Arsenic‐Affected Bangladesh Groundwater

Arsenotrophic bacteria contribute to the nutrient cycling in arsenic (As) affected groundwater. This study employed a culture‐independent and ‐dependent investigation of arsenotrophic microbiomes in As affected groundwater samples collected from Madhabpur, Sonatengra, and Union Porishod in Singair Upazila, Manikganj, Bangladesh. Total As contents, detected by Atomic Absorption Spectrophotometry (AAS) of the samples, were 47 µg/L (Madhabpur, SNGW‐1), 53 µg/L (Sonatengra, SNGW‐2), and 12 µg/L (Union porishod, SNGW‐3), whereas the control well (SNGW‐4; depths >150 m) showed As content of 6 µg/L. Denaturing Gradient Gel Electrophoresis (DGGE) analysis of the amplified 16S rRNA gene from As‐affected groundwater samples revealed the dominance of aerobic bacteria Pseudomonas within heterogeneous bacterial populations. DGGE of heterotrophic enrichments supplemented with arsenite [As (III)] for 4 weeks showed the dominance of Chryseobacterium, Flavobacterium, and Aquabacterium, whereas the dominant genera in that of autotrophic enrichments were Aeromonas, Acinetobacter, and Pseudomonas. Cultured bacteria retrieved from both autotrophic and heterotrophic enrichments were distinguished into nine genotypes belonging to Chryseobacterium, Acinetobacter, Escherichia, Pseudomonas, Stenotrophomonas, Janibacter, Staphylococcus, and Bacillus. They exhibited varying range of As(III) tolerance from 4 to 27 mM. As(III) transformation potential was confirmed within the isolates with oxidation rate as high as 0.143 mM/h for Pseudomonas sp. Sn 28. The arsenotrophic microbiome specifies their potential role in groundwater As‐cycling and their genetic information provide the scientific basis for As‐bioremediation.     

A bed‐load transport model for rough turbulent open‐channel flows on plane beds

Data from flume studies are used to develop a model for predicting bed‐load transport rates in rough turbulent two‐dimensional open‐channel flows moving well sorted non‐cohesive sediments over plane mobile beds. The object is not to predict transport rates in natural channel flows but rather to provide a standard against which measured bed‐load transport rates influenced by factors such as bed forms, bed armouring, or limited sediment availability may be compared in order to assess the impact of these factors on bed‐load transport rates. The model is based on a revised version of Bagnold's basic energy equation i_bs_b = e_bω, where i_b is the immersed bed‐load transport rate, ω is flow power per unit area, e_b is the efficiency coefficient, and s_b is the stress coefficient defined as the ratio of the tangential bed shear stress caused by grain collisions and fluid drag to the immersed weight of the bed load. Expressions are developed for s_b and e_b in terms of G, a normalized measure of sediment transport stage, and these expressions are substituted into the revised energy equation to obtain the bed‐load transport equation i_b = ω G ^3·4. This equation applies regardless of the mode of bed‐load transport (i.e. saltation or sheet flow) and reduces to i_b = ω where G approaches 1 in the sheet‐flow regime. That i_b = ω does not mean that all the available power is dissipated in transporting the bed load. Rather, it reflects the fact that i_b is a transport rate that must be multiplied by s_b to become a work rate before it can be compared with ω. It follows that the proportion of ω that is dissipated in the transport of bed load is i_bs_b/ω, which is approximately 0·6 when i_b = ω. It is suggested that this remarkably high transport efficiency is achieved in sheet flow (1) because the ratio of grain‐to‐grain to grain‐to‐bed collisions increases with bed shear stress, and (2) because on average much more momentum is lost in a grain‐to‐bed collision than in a grain‐to‐grain one. Copyright © 2006 John Wiley & Sons, Ltd.     

Relationship between canopy height and the reference value of surface conductance for closed coniferous stands

When estimating the dry‐canopy evaporation rate of coniferous stands using the Penman–Monteith equation, it is crucial to determine the reference value of surface conductance G_s. This paper examines the relationship between canopy height and the reference value of G_s based on the maximum value of G_s with a vapour pressure deficit ≥ 1·0 kPa, ?_{s max}. There is a clear correlation between canopy height and ?_{s max} when the projected leaf area index ≥3·0. This suggests that using this relationship will enable more accurate determination of the reference value of G_s for closed stands. Copyright © 2003 John Wiley & Sons, Ltd.     

Geochemistry of meteoric diagenesis in carbonate islands of the northern Bahamas: 2. Geochemical modelling and budgeting of diagenesis

Geochemical characterization and numerical modelling of surface water and ground water, combined with hydrological observations, provide quantitative estimates of meteoric diagenesis in Pleistocene carbonates of the northern Bahamas. Meteoric waters equilibrate with aragonite, but water‐ rather than mineral‐controlled reactions dominate. Dissolutional lowering of the undifferentiated bedrock surface is an order of magnitude slower than that within soil‐filled topographic hollows, generating small‐scale relief at a rate of 65–140 mm ka^?1 and a distinctive pocketed topography. Oxidation of organic matter within the subsoil and vadose zones generates an average P of 4·0 × 10^?3 atm, which drives dissolution during vadose percolation and/or at the water table. However, these dissolution processes together account for <60% of the average rock‐derived calcium in groundwaters pumped from the freshwater lens. The additional calcium may derive from oxidation of organic carbon within the lens, accounting for the high P of the lens waters. Mixing between meteoric waters of differing chemistry is diagenetically insignificant, but evapotranspiration from the shallow water table is an important drive for subsurface cementation. Porosity generation in the shallow vadose zone averages 1·6–3·2% ka^?1. Phreatic meteoric diagenesis is focused near the water table, where dissolution generates porosity at 1·4–2·8% ka^?1. Maximum dissolution rates, however, are similar to those of evaporation‐driven precipitation, which occludes porosity of 4·0 ± 0·6% ka^?1. This drives porosity inversion, from primary interparticle to secondary mouldic, vug and channel porosity. In the deeper freshwater lens, oxidation of residual organic carbon and reoxidation of reduced sulphur species from deeper anaerobic oxidation of organic carbon may generate porosity up to 0·06% ka^?1. Meteoric diagenesis relies critically on hydrological routing and vadose thickness (controlled by sea level), as well as the geochemical processes active. A thin vadose zone permits direct evaporation from the water table and drives precipitation of meteoric phreatic cements even where mineral stabilization is complete. Copyright © 2007 John Wiley & Sons, Ltd.     

Low-Temperature Oxidation of Magnetite in Loess-Paleosol Sequences: a Correction of Rock Magnetic Parameters

Low-temperature oxidation under atmospheric conditions affects the magnetic properties of magnetite in natural rocks: the coercivities of magnetite grains increase and other parameters change accordingly. It was recently shown that heating to 150°C largely removes the effects of low-temperature oxidation (van Velzen and Zijderveld, 1995). Heating may therefore serve as a detection tool for the presence of the effect of low-temperature oxidation. In the present study, a collection of loess and paleosol samples from various loess regions of the world is examined for the influence of low-temperature oxidation. In all samples of the collection a decrease of coercivities was found after heating to 150°C. Generally loess samples were affected to a larger extent than paleosol samples. The original range of remanent coercivities(B _cr)of 21-58 mT changed to 20-42 mT after heating. The IRM capacity of the samples decreased from 0 up to 25%. ARM showed changes between a decrease of 10% and an increase of 15%. The grain-size indicative parameter IRM/ARM is considerably influenced by the heating and therefore by low-temperature oxidation. The changes in susceptibility are limited and will not influence the interpretation of large-scale features of the susceptibility record as a paleoclimate proxy. Small variations, however, may be obscured by the varying influence of oxidation in the outcrop, which can significantly modify the rock-magnetic record. Rock-magnetic parameters used to determine magnetic mineral content and grain sizes should be corrected for the effect of low-temperature oxidation. To this end heating to 150°C is recommended. The occurrence of the changes is in itself already an indication for the presence of magnetite. Low-temperature oxidation will not only be due to recent weathering in the outcrop, but also to earlier oxidation processes in the source area, during transport and deposition of the loess and during pedogenesis. Truly fresh sediment samples are only influenced by this earlier oxidation. In that case heating will reveal the degree of ancient low-temperature oxidation, which may be related to climate at the time of deposition and pedogenesis.