Three-Dimensional Magnetotelluric Inversion: An Introductory Guide for Developers and Users

In the last few decades, the demand for three-dimensional (3-D) inversions for magnetotelluric data has significantly driven the progress of 3-D codes. There are currently a lot of new 3-D inversion and forward modeling codes. Some, such as the WSINV3DMT code of the author, are available to the academic community. The goal of this paper is to summarize all the important issues involving 3-D inversions. It aims to show how inversion works and how to use it properly. In this paper, I start by describing several good reasons for doing 3-D inversion instead of 2-D inversion. The main algorithms for 3-D inversion are reviewed along with some comparisons of their advantages and disadvantages. These algorithms are the classical Occam’s inversion, the data space Occam’s inversion, the Gauss–Newton method, the Gauss–Newton with the conjugate gradient method, the non-linear conjugate gradient method, and the quasi-Newton method. Other variants are based on these main algorithms. Forward modeling, sensitivity calculations, model covariance and its parallel implementation are all necessary components of inversions and are reviewed here. Rules of thumb for performing 3-D inversion are proposed for the benefit of the 3-D inversion novice. Problems regarding 3-D inversions are discussed along with suggested topics for future research for the developers of the next decades.     

About the Role of Quinones in the Action of Some Polyphenols on the Streaming of Protoplasm in Nitella sp. Cells

The concentration of phenols and quinones which stopped the protoplasmic movement in the Nitella cells after 15 min was determined. The quinones (β-naphthoquinone, α-naphthoquinone, p-benzoquinone, o-toluquinone, o-bromanil) stopped the protoplasmic movement in the concentration of (1 3) 10^?4 M, phenols (m-cresol, p-cresol, hydroquinone, guaiacol, phenol, gallic acid, pyrogallic acid, resorcinol) in the concentration of (0.2 5) 10^?2 M, except catechol – 2 10^?3 M. Very high toxicity of catechol and in the prolonged experiments (3 hours) also of hydroquinone is connected with the action of quinonoid productions of its oxidation. This suggestion is confirmed by the experiments:

• – by adding the phenol solutions to Nitella shoots (catechol, hydroquinone, resorcinol) we observed the greatest increase of oxygen absorption in case of catechol (86%), less in case of hydroquinone (38%), and for resorcinol oxygen absorption practically remained on the control level;
• – the action of catechol, hydroquinone and p-benzoquinone did not take place in the presence of glutathione and cysteine (but not cystine and oxidated glutathione);
• – diethyldithiocarbamate as an inhibitor of o-diphenoloxidase reduced the ability of catechol solutions to stop the protoplasmic movement;
• – the low concentrations of benzoquinones were able to stop the protoplasmic movement;
• – for stopping the protoplasmic movement under the prolonged time of incubation from 15 min to 3 hours there was necessary a lower concentration of solutions of hydroquinone and catechol in comparison with resorcinol.

     

太湖北部典型乔木冠层对酸性降雨的中和作用

2003年6—7月梅雨期间,于太湖北部测定大气降雨、典型林冠穿透雨和地表径流水等样品的pH和N、P等营养元素化合物离子浓度,结果表明,林冠层穿透水pH平均值比大气自然降水高约1.2个pH单位,其中和酸性物质效率为82%-97%,中和能力显示出阔叶树大于阔、针叶混交树,阔、针叶混交树大于针叶树的规律,并计算比较了乔木冠层和草坪、村镇地表径流水相对于自然降水中的TN、TP比值.从而得出,树木冠层穿透水中的离子浓度的变化是对酸沉降的一种积极的响应.     

Fatty Acid Composition of Plankton and Bighead Carp (Aristichthys nobilis) in Freshwater Ponds

The community structure and fatty acid composition of plankton in broodstock ponds were studied at the Bishui Fisheries Company in the Liaoning Province, northeast China, between May and December 2002 and in March 2003. The Fatty acid analysis of bighead carp larvae and plankton in the fry pond occurred during June, July, and September 2002. The fatty acid composition of the plankton varied with seasonal changes in the community structure. When blue‐green algae dominated the broodstock ponds in spring and summer, the percentage of saturated fatty acids (SFA) (especially 16:0) was high. When diatoms and cryptophytes dominated in autumn and winter, the percentage of polyunsaturated fatty acids (PUFAs) (mainly n–3 PUFA) was high. Similarly, a high content of docosahexaenoic acid (DHA) occurred in autumn and winter when DHA‐rich copepods became an important group of zooplankton. In addition, environmental factors, especially water temperature, influenced the fatty acid composition of plankton. 16:0, DHA, and 18:1n–9 were dominant fatty acids of bighead carp larvae during ontogeny. 16:0, C18 unsaturated fatty acids, and eicosapentaenoic acid (EPA) were major fatty acids of plankton in the fry pond. Analysis of the relationship between the fatty acids of the larvae and those of plankton showed that the fatty acid profiles of the larvae did not always agree with those of plankton.     

Use of Thin-Layer and Paper Chromatography for Detection of Ortho- and Para-Quinones Formed in the Course of Phenol Oxidation

In order to detect the labiles in the aqueous solution of the benzene- and naphthoquinones, they were preliminarily transformed with the aid of the benzene sulphinic acid into stable sulphonic derivatives. Methods were developed of the chromatographic detection on paper and in a thin layer of the β-naphthol, phenol, ortho-, para-dioxybenzenes and their sulphonic derivatives with joint presence in the solution of ortho- and para-isomers of the dioxyderivatives. For the chromatographic separation of the ortho- and para-derivatives, the ability of ortho-isomers to form chelate complexes with boric acid or to precipitate with mean laed acetate salt was made use of. With the aid of the given method, the stage of the quinone formation in the course of abiogenic and biochemical (under the action of Nitella sp.) oxidation of benzene, phenol, β-naphthol, pyrocatechol, hydroquinone has been proved. Oxidation under the action of Nitella sp. leads to the formation of the dioxybenzene ortho-isomers and their derivatives.     

Bio‐based Ester Oils for Use as Lubricants in Metal Working

The potential application of bio‐based ester oils for use as lubricants in metal working has been investigated for sustainable production processes in the future. When waste edible and animal fats came into focus as starting materials, it was already proven, that ester oils produced from plant fats performed very well as cooling lubricants. Waste fats were first characterized by analyzing and monitoring samples for one complete year. Inorganic and organic contaminations were found to be low and without seasonal variations. Fatty acid methyl esters (FAME) were produced by transesterification of the waste fats and they were separated into fractions with saturated FAME or unsaturated FAME by fractional crystallisation (winterisation). Further transesterification with 2‐ethylhexanol led to products that could be successfully tested as lubricants. The development of an extraction process aimed at the recycling of oil containing grinding mud by enabling the recirculation of lubricating oil and reutilization of oil‐free metal chips.     

Acid Rain and Natural Organic Matter (NOM)

Twentyfive years of research on the effects of acid rain on rivers and lakes has, to a very small extent, documented changes in the nature and properties of natural organic matter (NOM). In Western Norway, a "whole-watershed-artificial-acidification-experiment" took place in the period 1988–1996. The goals of this long-term experiment were to study the role of NOM in acidification of surface water and the effects of acid precipitation on the quality and properties of NOM. In the HUMEX project (Humic Lake Acidification Experiment) one half of a lake and the corresponding catchment was artificially acidified with H₂SO₄ and NH₄NO₃ over a period of 5 years. The other half of the lake and catchment served as a control. In addition to monitoring of the general chemical composition of the water from the two lake halves, a number of other chemical and biological characteristics were studied. Here, we report the results related to changes in the nature and chemical properties of NOM. During the first few years of acidification, a significantly lower concentration of NOM was recorded in the acidified half of the catchment, compared with the control. However, statistical analyses of all data (covering a 2-years pre-treatment period and 5 years of treatment) related to the concentration of NOM (TOC, colour, and UV absorbance) did not suggest any significant effect on the quantity of NOM. This apparent discrepancy between the initial decrease in the concentration of NOM and no effect when the whole 5-years period is considered, may be due to the results of two different simultaneous processes. The results suggest that there first was a reduction of TOC and colour, as a consequence of the acidification, followed by an increase, perhaps owing to increased fertilisation (nitrogen) and in addition to a general temperature increase during the period. In addition, short-term studies of the aquatic surface microlayers, lipophilicity of the NOM, content of organic sulfur, and molecular size indicate differences in the quality of the NOM between the two lake halves, which could affect light absorption.     

Effect of Individual Phenolic Compounds and of Their Mixtures on Luminous Bacteria. Part 2: Interaction of p- and o-Diphenol Toxicity for Beneckea harveyi with Their Oxidation

Experimental material was obtained supporting a hypothesis on the interaction between p- and o-diphenol toxicity and their oxidation. It is shown that quinones – the products of pyrocatechol and hydroquinone oxidation – possess increased toxicity towards luminous bacteria cells.     

Mobilisierbarkeit von hydrophoben organischen Schadstoffen in belasteten Böden und Abfällen. Teil I: Mobilisierbarkeit von PCB,PAK und n-Alkanen durch Lösungsvermittler

Mobilization Potential of Hydrophobic Organic Compounds (HOCs) in Contaminated Soils and Waste Materials. Part I: Mobilization Potential of PCBs, PAHs, and Aliphatic Hydrocarbons in the Presence of Solubilizing Substances When using an elution procedure for organic pollutants to estimate the leaching behaviour of contamined soils and waste deposits, the influence of organic matter in solids and eluates adequately has to be considered. In batch tests with a solid/liquid ratio of 1:10, various aqueous solutions were composed, the solubilizing effect of which can be attributed to ubiquitous natural compounds (e. g., phospholipids, humic and carbonic acids). These solutions were evaluated in regard to the mobilization of PAHs, PCBs, and aliphatic hydrocarbons in soil and waste samples. The results were compared with batch tests containing sodium dodecyl sulfate (SDS), the properties and applications of which are selected and optimized in order to simulate the chemical interactions between pollutant and solubilizing substances of natural sources. Under alkaline conditions, the part of eluated pollutants was high because of the release of humic substances indigenous to the sample. Low concentrations of phospholipids and humic acid could decrease the mobility of aliphatic hydrocarbons. The extend of HOC mobilization is affected by specific interdependences between solubilizing substances and reactive matter of the samples. For most samples, 5.0 g/L concentrated SDS solution was able to simulate the most effective natural solutizer potential in regard to the mobilization of PAHs, PCBs, and aliphatic hydrocarbons within the system of batch tests. Whereas elution with pure water caused significant deviations in pollutant composition and too low yields, the use of SDS effected à good conformity. Modified in such a manner, the elution procedure can follow DIN 38414 part 4, when loss of pollutants will be minimized; e. g., centrifugation is needed to separate phases.     

太湖流域降雨和湖水酸根阴离子长期变化及其环境意义

为揭示太湖流域降雨和湖水酸根阴离子长期变化特征及环境意义,通过历史数据收集和采样分析,对太湖流域降雨和湖水中的SO₄^2-、NO₃^-变化特征和来源进行了研究.结果表明：自1990s以来太湖流域降雨中SO₄^2-呈显著下降趋势,年平均下降率为0.28 mg/（L·a）;NO₃^-浓度却呈显著上升趋势,年平均增长率为0.05 mg/（L·a）,降雨中氮污染呈现加重的趋势.与之相反,湖水中SO₄^2-呈显著上升趋势,年平均增长率为1.24 mg/（L·a）;NO₃^-浓度却呈显著下降趋势,年平均下降率为0.02 mg/（L·a）.30年以来,太湖水体SO₄^2-/NO₃^-比值不断升高,远高于降水SO₄^2-/NO₃^-比值.研究认为：流域SO₂排放引起的酸沉降是湖水SO₄^2-浓度增长的最重要原因,但氮氧化物排放并未引起湖水NO₃^-浓度升高,说明太湖流域对大气沉降的氮氧化物有滞留作用,而太湖水体是流域大气沉降硫酸盐的重要汇.综合治理太湖流域酸性物质排放对防止太湖水体酸化和治理富营养化都具有重要意义.     

The Analysis of the Seasonal,Spatial, and Compositional Distribution of Humic Substances in a Subtropical Shallow Lake

The spatial and temporal distribution of humic substances in aquatic ecosystems can have important effects on ecosystem productivity, negatively impacting primary productivity while positively impacting secondary productivity. In the present investigation, a large shallow lake ecosystem was studied to determine the spatial and seasonal variation of the composition and concentration of humic substances. Concentrations of total dissolved organic matter, humic acid, and fulvic acid were found to display significant spatial distributions (1.3…13.5 mg/L, DOM; 0.1…5.4 mg/L, HA). The distribution is described by using mapping techniques and the analysis of the spatial distribution of the lake. An analysis of the seasonal variations also indicated the dependence of the occurrence of these compounds on meteorological and hydrological conditions. To identify the potential sources of these organic materials, an analysis was made of the ratio of humic and fulvic acid fractions and total DOM. It was found that areas of high DOM concentration coincided with the areas of highest HA percentage of total DOM. Furthermore using the ratio of the normalised concentrations of HA, FA, and residual DOM (< 5000 g/mol) it was found that areas dominated by each are spatially distinct. This confirms the hypothesis that in these shallow lakes, photodegradation and bacterioplankton activity will create a residence time dependent zonation of each component of the total DOM.     

Operational Cost Comparison of Several Pre‐Treatment Techniques for OMW Treatment

Olive mill wastewaters (OMWs), which are known to have deep impacts on the receiving water bodies due to their high‐strength contents of organic materials and color, must be treated before discharge. For this reason; a number of research studies have been available in current literature related to the treatment of OMWs. However, no widely accepted treatment alternatives have been proposed yet. The common results of these studies suggest that OMWs must be pretreated prior to final purification processes. This study focuses on the comparison of alternative pre‐treatment processes in the aspect of chemical oxygen demand (COD) removal and costs of operation. Centrifuging, lime precipitation, acid cracking, and electrocoagulation processes were performed to compare removal efficiencies and operational costs. The COD removal efficiencies for centrifuging, lime precipitation, acid cracking, and electrocoagulation processes were determined to be 30.1, 24.1, 20.0, 53.7%, respectively, with operational costs being $0.30, $0.37, $1.42, and $11.60 per cubic meter of wastewater treated, respectively. The centrifuging process was concluded to be the most appropriate one according to the COD removal efficiency and cost of operation.     

Some Methods of Phenol Elimination from Sewage Waters. Part 1: Biodestruction by the Vegetable Homogenates

The different phenoloxidase contents of shoots of various land plants (sunflower, corn, wheat, potato) as well as of various algal species were used for investigating the biochemical conversion and accumulation of phenol, p-and o-cresol, guaiacol, pyrocatechol and hydroquinone. The methods applied for processes and analyses are described. The results of the investigations are summarized in several tables and graphical representations.     

Adsorptive Removal of Acid Blue 15: Equilibrium and Kinetic Study

Activated carbons prepared from sunflower seed hull have been used as adsorbents for the removal of acid blue 15 (AB‐15) from aqueous solution. Batch adsorption techniques were performed to evaluate the influences of various experimental parameters, e. g., temperature, adsorbent dosage, pH, initial dye concentration and contact time on the adsorption process. The optimum conditions for AB‐15 removal were found to be pH = 3, adsorbent dosage = 3 g/L and equilibrium time = 4 h at 30°C. The adsorption of AB‐15 onto the adsorbent was found to increase with increasing dosage. It was found from experimental results that the Langmuir isotherm fits the data better than the Freundlich and Temkin isotherms. The maximum adsorption capacity, Q_m (at 30°C) was calculated for SF1, SF2, and SF3 as 75, 125 and 110 mg g^–1 of adsorbent, respectively. It was found that the adsorption follows pseudo‐second order kinetics. The thermodynamic parameters such as ΔG°, ΔH°, and ΔS° were also evaluated. The activated carbons prepared were characterized by FT‐IR, SEM and BET analysis.     

A quantitative evaluation of pyrite weathering

Namurian sediments at Mam Tor, Derbyshire are cut by a major landslide and a geological fault. Both channel oxygenated waters into fragmented pyritic shales. Pyrite is rapidly oxidized to sulphuric acid, 1.5 g being destroyed by each litre of water passing through the fault-crush. More than 99 per cent of the acid, however, is immediately consumed in clay-mineral transformation and carbonate dissolution reactions. The typical acid-sulphate ‘ochre’ springs thus retain less than 1 per cent of the acid generated in the crush zone. These very rapid and large scale chemical transformations probably contribute to the slide's continuing activity.     

Electro‐Fenton Treatment of Photographic Processing Wastewater

In this work, the treatment of photographic processing wastewaters (PPW) by electro‐Fenton process has been investigated. The Influence of operating conditions on kinetics and efficiency of electro‐Fenton process has been evaluated using carbon felt cathode and platinium (Pt) or boron‐doped diamond (BDD) anode. The results of electro‐Fenton treatment of PPW have shown that nearly complete removal of total phenols was obtained for all combinations with pseudo‐first rate constants of 0.07, 0.012, and 0.018/min for carbon felt/Pt, carbon felt/BDD and Pt/BDD cathode/anode combinations, respectively. The combination of carbon felt cathode with BDD anode achieved the highest total organic carbon (TOC) removal of 90%, while it did not exeed 40% for carbon felt/Pt combination. Increasing current intensity and Fe²⁺ dose enhances the efficiency of electro‐Fenton process. However, increasing pH decreases TOC removal during the treatment of PPW by electro‐Fenton process. The highest efficiency of electro‐Fenton process using BDD anode can be explained by the contribution of direct and indirect oxidation routes in the degradation mechanism of organics including (i) oxidation via hydroxyl radicals generated from the catalytic decomposition of H₂O₂ and from water discharge on BDD anode, (ii) direct oxidation of certain organic compounds on BDD anode, and (iii) mediated oxidation with inorganic oxidants electrogenerated from anodic oxidation of supporting salts.     

Effect of Individual Phenolic Compounds and of their Mixtures on Luminous Bacteria. Part 7: Change of Polyphenol Toxicity in the Presence of their Oxidases and Certain Practical Problems

Data are presented on the toxicity of hydroquinone and pyrocatechol in the presence of protein preparations possessing oxidase activity. Problems are discussed of their use as biologically active means.     

Methods of Analyzing Quinones in Water and Their Application in Studying the Effects of Hydrophytes on Phenols. Part 4: Accumulation of Exogenic Phenols,Localization of Endogenic Phenols and o-Diphenol Oxidase in Nitella Cells

By using Nitella, with the aid of a technique which is described in detail the uptake of resorcinol by the cytoplasm was demonstrated and quantitatively determined under different test conditions. In contrast to the phenol oxidation products of hydroquinone and pyrocatechol, the further “fate” of the resorcinol taken up by the cell substance is not yet fully clear. The rate of resorcinol absorption has been defined with a permeability constant.     

Acid rain damage to carbonate stone: A quantitative assessment based on the aqueous geochemistry of rainfall runoff from stone

An onsite experimental procedure was used to identify and quantify acid rain damage to carbonate stone, based on the change in rain runoff chemical composition. Observed changes in runoff from stone are attributed to the interaction of acidic species present in the rain with the stone surface. Onsite data obtained during the summer and fall of 1984 at three locations in the northeastern United States indicate that carbonate stone surface recession is related to acid deposition. Although the study is continuing, current data are not adequate to distinguish differences in the acid-stone reaction between limestone and marble nor among the three study sites. A single linear relation between carbonate stone surface recession (the dependent variable) and hydrogen ion loading to the stone surface (the independent variable) appears to describe the data set.     

Cooxidation of Carcinogenic Benzo(a) Pyrene and Phenols by Horseradish Peroxidase (Armoracia lapathifolia)

The catalytic activity of horseradish (Armoracia lapathifolia) peroxidase in the oxidation reactions of benzo(a)pyrene (BP) and phenols, separately and in admixture, has been studied. Experiments were carried out with model phenols from industrial sewage (phenol, m-, p-cresols, catechol, hydroquinone, resorcinol, orcinol), keeping to the real concentration ratio of reagents, 0.5 mM for phenols, 0.1 nM for benzo(a)pyrene. The total oxidation process for all reagents tested is described by the second-order formal kinetic equation up to 60 … 90% of their conversion. Addition of peroxidase increases the rate of oxidation of benzo(a)pyrene and phenols 2 … 6 times as compared with the control test (with hydrogen peroxide), whereas a linear dependence of the rate of benzo(a)pyrene oxidation on the enzyme concentration is observed. By cooxidation a mutual inhibition of benzo(a)pyrene and phenols is established whose degree depends on the phenol-chemical structure and varies in the range of 23 … 58% for BP under the influence of phenols and 35 … 80% for phenols under the influence of benzo(a)pyrene. The results obtained permit a supposition that peroxidase containing plants are capable of simultaneously transforming carcinogenic benzo(a)pyrene and toxic phenols in water reservoirs and in the soil, thus promoting the detoxication of environment.