The electrical conductivity of Posidonia black shales — from magnetotelluric exploration to rock samples

We carried out a magnetotelluric field campaign in the South–East Lower Saxony Basin, Germany, with the main goal of testing this method for imaging regional Posidonia black shale sediments. Two‐dimensional inversion results of the magnetotelluric data show a series of conductive structures correlating with brine‐saturated sediments but also with deeper, anthracitic Westphalian/Namurian coals. None of these structures can be directly related with the Posidonia black shale, which appears to be generally resistive and therefore difficult to resolve with the magnetotelluric method. This assumption is supported by measurements of electrical resistivity on a set of Posidonia shale samples from the Hils syncline in the Lower Saxony basin. These rock samples were collected in shallow boreholes and show immature (0.53% Ro), oil (0.88% Ro), and gas (1.45% Ro) window thermal maturities. None of the black shale samples showed low electrical resistivity, particularly those with oil window maturity show resistivity exceeding 10⁴ Ωm. Moreover, we could not observe a direct correlation between maturity and electrical resistivity; the Harderode samples showed the highest resistivity, whereas the Haddessen samples showed the lowest. A similar trend has been seen for coals in different states of thermal maturation. Saturation of the samples with distilled and saline water solutions led to decreasing electrical resistivity. Moreover, a positive correlation of electrical resistivity with porosity is observed for the Wickensen and Harderode samples, which suggests that the electrical resistivity of the Posidonia black shale is mainly controlled by porosity.     

有机质对纳米级磁铁矿热稳定性的影响

单畴磁铁矿颗粒是地质样品中最重要的磁性载体,其稳定性一直备受关注.为了认识有机质对纳米级磁铁矿颗粒热稳定性的影响,本文对比研究了趋磁细菌AMB-1合成的单畴磁铁矿分别在全细胞中和经去胞提纯后的纯化磁小体中的热磁性质,以及热处理后样品的磁滞参数和低温磁性的变化.发现仅有磁小体膜包裹的纯化磁小体中单畴磁铁矿热稳定性极强,而全细胞中的单畴磁铁矿加热过程中发生了显著的热变化:磁铁矿在约270℃即开始转化,400℃以前几乎完全被有机质还原为顺磁性物质;同时在400℃以前,有机质的还原作用与有机质热分解引起磁小体链的坍塌,共同导致了样品矫顽力(Bc)、剩磁矫顽力(Bcr)和剩磁比(Mrs/Ms)的减小,以及矫顽力比(Bcr/Bc)的增加. 我们的实验结果清楚地表明,当地质样品中含有较多有机质组分并受热事件影响时,其中的单畴磁铁矿难以得到保存.     

Adjoint method for the optimum planning of industrial pollutant sources

The deterioration of air quality is threatening the life and health of people. Scientists in China and other countries have done a great deal of research work on the details of air pollution and the methods of preven-tion and control during the past decades. Up to now, most of the achievements are concentrated on the techniques of controlling pollutant sources and the programs of reduction, which focus on the improve-ment of air quality and the restoration of environment. The techniques of con…     

Time-resolved Fluorescence Measurements of Aquatic Natural Organic Matter (NOM)

The fluorescence decay of aquatic natural organic matter (NOM) samples was investigated using the time-correlated single photon counting technique (TCSPC). Two different approaches for the data analysis are presented: the discrete component approach (DCA) and the exponential series method (ESM). The parameter set obtained in the DCA is discussed in terms of characterization for NOM of different origins. However, the obtained parameter set can only be interpreted as operationally defined. Using the ESM for a fluorescence decay time distribution analysis no a priori assumption about the number of fluorescing components was introduced into the data analysis. The interpretation of fluorescence decay time data for samples before and after ozonation is in good agreement with results of other analytical methods.     

Tracing of Peroxidase Activity in Humic Lake Water

An enzyme assay was developed for studies on peroxidase activities in humic lake water. 3,4-Dimethoxybenzyl alcohol (veratryl alcohol, VeraOH) was used as tracer substrate, and peroxidase (EC 1.11.1.7) activity was measured by high-performance liquid chromatography. The chemical stability of VeraOH and its application as peroxidase substrate was tested under light and dark conditions, different hydrogen peroxide (H₂O₂) concentrations and humic matter contents. VeraOH was stable under low UV radiation at in situ conditions in lake water (<0.010...0.25 kJ m^–2 d^–1), laboratory conditions (<0.05...0.30 kJ m^–2 d^–1), and low (1...100 μM) H₂O₂ concentrations. However, peroxides oxidized VeraOH above 1...10 mM H₂O₂ concentration in sterile Millipore-Q and humic lake water. Dark incubations showed little VeraOH oxidation products. The developed peroxidase assay was tested in the growth medium of Phanerochaete chrysosporium and a bacteria isolate (P.M.D. 20.4.3.1) from mesohumic lake Pääjärvi. Peroxidase activities were also measured in natural microbial communities under standard laboratory and under in situ conditions in humic lake water. Incubation times of about 5 to 12 days were usually needed to record significant (P < 0.05) peroxidase activities, in lake waters. In situ peroxidase activities varied in pelagial surface water (0...0.5 m) on a seasonal scale between 74 nmol L^–1 h^–1 and 273 nmol L^–1 (mean: 176 nmol L^–1 h^–1) and within the water column between 110 nmol L^–1 h^–1 and 800 nmol L^–1 h^–1 (mean: 500 nmol L^–1 h^–1) in polyhumic lake Mekkojärvi.     

Pathlines of pollutant migration in groundwater of the Visakhapatnam urban area,India

The groundwater regime in the north‐western part of the Visakhapatnam urban area was polluted as early as 1981 by discharge of untreated industrial effluent from a Hindustan Polymers Limited (HPL) plant. A total dissolved solids (TDS) concentration of surficial effluent up to 6500 mg/l and of groundwater in the range 3000–4200 mg/l has been reported in the environs of the HPL plant during May 1992. Groundwater occurs under water table conditions. The groundwater flow model was simulated as a single layer aquifer, using MODFLOW and FLOWPATH computer models. Aquifer parameters were estimated and the value of effective porosity assumed. The water table configuration was mapped in May 1981 using 33 observation wells. The calibrated hydraulic head distribution was used to compute the velocity field using the effective porosity values. The flow paths of groundwater migration from the source locations up to 2002 AD were predicted. Pathlines of particles in the groundwater indicated a predominant north‐east and south‐west migration of groundwater pollution in the area. Copyright © 1999 John Wiley & Sons, Ltd.     

Formation of Humic-like Substances in Mixed and Pure Cultures of Aquatic Microorganisms

A natural decay of plant and animal biomass in aquatic environments results in the release of different simple structured organic substances into water. In our laboratory experiments we investigated whether some of them, e.g., starch or peptone, and also a complex yeast biomass can be transformed into humic-like substances by natural assemblages and some pure cultures of aquatic microorganisms. After a 6 months incubation most of the cultural media enriched with those natural organic substrates turned dark in color and humic-like substances (HS) could be isolated. However, the original substrate organic carbon was mainly mineralized in microbial cultures, and only about 3 % C was converted into HS. Total yields of HS differed in dependence of the individual substrate used (peptone > yeast > starch), the origin of inoculum (river > lake > groundwater), and the incubation temperature (20°C > 10°C). According to their elemental composition, and their spectroscopical and electrophoretic characteristics the microbially formed HS resembled natural aquatic humic matter, but were higher in aliphatic constituents (carbohydrates, peptides) and lower in aromatic structures. HS-like substances were also obtained from pure cultures of a bacterium Bacillus sphaericus and a fungus Cladosporium cladosporioides. The ¹³C and ¹⁵N isotopic contents of the microbially produced HS differed in dependence on the microbial inoculum and the type of organic substrates used, but in general they indicated anabolic processes to be mainly responsible for the humification of the simple organic substrates used in our experiments.     

Total Organic Carbon (TOC) as a Sum Parameter of Water Pollution in Selected Polish Rivers (Vistula,Odra, and Warta)

This paper reports on total organic carbon (TOC) and its fractions dissolved organic carbon (DOC) and particulate organic carbon (POC) studied in different Polish rivers. The samples investigated came from the Vistula, Odra, and Warta rivers, and were compared with similar data on river waters available in the literature. The DOC concentrations ranged from 10.0 to 14.2 mg/L and did not vary during the vegetative season. The POC values considerably increased from May through September and reached a maximum in summer. Results for the years 1991τ1996 evidenced a significant increase in the POC value for the Polish rivers from 10.8 to 24.5 mg/L, in comparison with analogous values for West European rivers and North American ones. The enhanced values of TOC and POC were interpreted as being due to anthropogenic pollution.     

Electro‐Catalytic Degradation of Phenol Organics with SnO2‐Sb2O3/Ti Electrodes

The effect of extraordinary degradation of phenol organics on the SnO₂‐Sb₂O₃/Ti electrode is investigated through experimental research and theoretical analysis. The phenol organics contained 4‐chloro‐phenol, 4‐bromo‐phenol, and 2‐iodo‐phenol. At a current density of 4 mA cm^–2 and an electrolysis time of 12 h, the degradation efficiency of the phenols was over 98% with a relatively short degradation time, whereas the degradation time of the PbO₂/Ti electrode surpassed 40 h while delivering 100% disposal efficiency. Therefore, the effectiveness of electrochemical (EC) oxidation by the SnO₂‐Sb₂O₃/Ti was superior to that of the PbO₂/Ti electrode. At the same time, the SnO₂‐Sb₂O₃/Ti had higher oxygen generation potential and lower electron consumption than the other electrodes. This was mainly due to the effect of the middle Sb₂O₃ layer, which due to its high porosity and good catalytic effect, contributed to a better catalysis than the SnO₂ part.     

Assessment of the ecological quality status of soft-bottoms in Reunion Island (tropical Southwest Indian Ocean) using AZTI marine biotic indices

The ability of the two synthetic marine biotic indices, AMBI and M-AMBI, to account for changes in the ecological quality of coastal soft bottoms of Reunion Island according to disturbances was assessed from macrobenthic samples collected in five sectors between 1994 and 2004. Samples were collected under non-perturbed conditions and at two sites subjected to heavy organic enrichment. Both indices are based on a classification of macrofauna into ecological groups (EG), and their transfer to tropical waters required some adaptations. These indices proved efficient in detecting a degradation of habitat quality. Their use resulted in the classification of all sites sampled between 1996 and 1998 as "good" or "high". M-AMBI nevertheless tended to result in the attribution of a slightly worse ecological quality status than AMBI. Together with an update of the EG species list for the Indian Ocean area, our results support the extension of both indices for the assessment of tropical soft bottoms.