Toxic effects of Irgarol 1051 on phytoplankton and macrophytes in Lake Geneva

Irgarol 1051 is a recent herbicidal compound, inhibitor of photosynthesis, used in antifouling paints. This toxic is persistent in aquatic environments, with low abiotic and biotic degradation, highly phytotoxic, and has already been detected in estuaries and coastal areas, with suspected negative impacts on non-target organisms (aquatic plants and algae). We measured the toxicity of Irgarol 1051 to macrophytes and phytoplankton from Lake Geneva (between Switzerland and France) by determining chlorophyll fluorescence yield, and phytoplankton primary production. Long-term toxicity for phytoplankton was estimated in a microcosm study, and growth inhibition tests were performed with isolated algal strains. The concentration of Irgarol 1051 was analysed in the water, and the most polluted site showed a higher level (up to 135 ng/L) than the lowest observed effect concentration for phytoplankton (8-80 ng/L), while the macrophytes appeared to be more tolerant to Irgarol 1051 in short-term tests. The microcosm study showed that phytoplankton structure might be even more sensitive to Irgarol 1051.     

西藏南部地区人工爆炸地震探测的地壳结构

众所周如,西藏地区是研究地球深部结构和构造的窗口,是研究大陆板块学说的重要场所,也是寻找热源和其它矿产资源的有利地区.因此,世界各国地学科学家都希望在本地区进行科学研究工作,或与我国科学工作者协作共同探索这一重要地区.中国和法国的地质、地球物理科学家经商讨共同组成“中法喜马拉雅山地质研究队”,对西藏中部广大地区进行地质、地球物理的科学研究工作.深部地震探测是地球物理研究中的重要内容.中法双方共同决定,在中国西藏南部的日喀则地区至北边的那曲地区作地震探测工作.为了探测地壳上地幔的结构,1981年在西藏的南部佩枯错至普莫雍错500公里的喜马拉雅山北麓——雅鲁藏布江地区进行了人工爆炸地震探测工作.本文是中法地质研究队合作的深部地震探测资料的解释结果.     

New methods for the determination of hydrogen content of aluminum and its alloys: Part I. Improvements in the vacuum extraction method

The vacuum hot extraction method, first proposed by Ransley for the determination of hydrogen content of aluminum and its alloys, was systematically investigated to check if it could be considered as a reference procedure for the development of other methods directly applicable in routine work. For that, the use of an improved apparatus involving a mass spectrometer as gas detector and specimens intentionally charged with deuterium —a tracer whose properties are similar to those of hydrogen—permits the following conclusions: 1) The method is correct for any alloy, even for all the alloys with a high magnesium or zinc content, 2) The “getter effect” which could lead to inaccurate results does not occur, provided the pumping speed of the transfer pump exceeds the rate of outgassing from the sample, 3) The extraction from the solid phase seems to be complete, since results obtained in this condition are not significantly different from those obtained from melted samples. 4) The time required for an analytical determination (several hours) due essentially to the preliminary operations, cannot be practically reduced by extraction at higher temperature in the liquid state. The Ransley method can thus be considered as a reference method for checking other more practical methods.     

Nonlinear Convective Oscillations in Two-Layer Systems under the Action of the Horizontal Component of the Temperature Gradient

The influence of the horizontal component of the temperature gradient on nonlinear oscillatory convective flows, developed under the joint action of buoyant and thermocapillary effects in the 47 v2 silicone oil - water system, is investigated. The layers of equal thicknesses are considered. Transitions between nonlinear regimes of convection, have been studied. It is shown that under the action of the horizontal component of the temperature gradient, the asymmetric oscillatory flow takes place in the system.     

Mass spectrometry-based metabolomics: accelerating the characterization of discriminating signals by combining statistical correlations and ultrahigh resolution

A strategy combining autocorrelation matrices and ultrahigh resolution mass spectrometry (MS) was developed to optimize the characterization of discriminating ions highlighted by metabolomics. As an example, urine samples from rats treated with phenobarbital (PB) were analyzed by ultrahigh-pressure chromatography with two different eluting conditions coupled to time-of-flight mass spectrometric detection in both the positive and negative electrospray ionization modes. Multivariate data analyses were performed to highlight discriminating variables from several thousand detected signals: a few hundred signals were found to be affected by PB, whereas a few tenths of them were linked to its metabolism. Autocorrelation matrices were then applied to eliminate adduct and fragment ions. Finally, the characterization of the ions of interest was performed with ultrahigh-resolution mass spectrometry and sequential MS(n) experiments, by using a LC-LTQ-Orbitrap system. The use of different eluting conditions was shown to drastically impact on the chromatographic retention and ionization of compounds, thus providing a way to obtain more exhaustive metabolic fingerprints, whereas autocorrelation matrices allowed one to focus the identification work on the most relevant ions. By using such an approach, 14 PB metabolites were characterized in rat urines, some of which have not been reported in the literature.     

NO ions as IR probes for the location of OH groups and Na ions in main channels and side pockets of mordenite

NO⁺, generated from NO and O₂, is an infrared probe for the differentiation of Brønsted sites in the main channels and side pockets of mordenites, and for the location and accessibility of sodium ions in the structure. Na⁺ ions in cationic positions in the main channels are replaced by NO⁺, and sodium nitrate is formed. The band assignment was checked by isotopic experiments.     

Aluminum drinking water treatment residuals (Al-WTRs) as sorbent for mercury: Implications for soil remediation

The potential of readily available and non-hazardous waste material, aluminum drinking water treatment residuals (Al-WTRs), to efficiently sorb and immobilize mercury (Hg) from aqueous solutions was evaluated. Al-WTR samples with average specific surface area of 48m(2)/g and internal micropore surface area of 120m(2)/g were used in a series of batch sorption experiments. Obtained sorption isotherms indicated a strong affinity of Hg for Al-WTRs. Using the Langmuir adsorption model, a relatively high maximum sorption capacity of 79mg Hg/g Al-WTRs was determined. Sorption kinetic data was best fit to a pseudo-first-order model, while the use of the Weber-Morris and Bangham models suggested that the intraparticle diffusion could be the rate-limiting step. Also, Al-WTRs effectively immoblized Hg in the pH range of 3-8. The results from these short-term experiments demonstrate that Al-WTRs can be effectively used to remove Hg from aqueous solutions. This ability points to the potential of Al-WTRs as a sorbent in soil remediation techniques based on Hg-immobilization.     

Sensitivity of CFP/YFP and GFP/mCherry pairs to donor photobleaching on FRET determination by fluorescence lifetime imaging microscopy in living cells

Fluorescent protein-based FRET is a powerful method for visualizing protein-protein interactions and biochemical reactions in living cells. It can be difficult, however, to avoid photobleaching when observing fluorescent cells under the microscope, especially those expressing CFP. We compared the sensitivity of two protein-based FRET pairs to light-induced fluorescence changes in the donor, on FRET determination by fluorescence lifetime imaging microscopy (FLIM). Thanks to the very low excitation light levels of the time- and space-correlated single photon counting (TSCSPC) method, FLIM acquisitions were achieved without donor photobleaching. Here, we show that photobleaching of CFP by a mercury lamp under the microscope induced a decrease in the mean fluorescence lifetime, which interfered with FRET determination between CFP and YFP. Importantly, the range of light-induced variation of the mean fluorescence lifetime of CFP was not proportional to the decrease in the steady state fluorescence intensity and varied from cell to cell. The choice of the CFP/YFP pair therefore requires that the cells be observed and analyzed at very low light levels during the whole FRET experiment. In contrast, the GFP/mCherry pair provided an accurate FRET measurement by FLIM, even if some GFP photobleaching took place. We thus demonstrate that CFP can be an unreliable donor for FRET determination in living cells, due to its photosensitivity properties. We demonstrate that the GFP/mCherry pair is better suited for FRET measurement by FLIM in living cells than the CFP/YFP pair.     

Engineering of protein epitopes: a single deletion in a snake toxin generates full binding capacity to a previously unrecognized antibody

Structural features associated with the ability of a monoclonalantibody (mAb) to discriminate between protein variants areidentified and engineered. The variants are the curaremimetictoxin from Naja nigricollis and erabutoxin a or b from Laticaudasemifasciata which differ from each other by 16 substitutionsand one insertion. The neutralizing mAb M1 recognizes with highaffinity a topographical epitope on the surface of toxin , butfails to recognize the erabutoxins although they possess mostof the residues forming the presumed epitope. Examinations ofthe toxin and erabutoxin 3-D structures and molecular dynamicssimulations reveal several differences between the variants.In particular, the region involving the ß-turn 17–24is organized differently. Analysis of the differences foundin this region suggests that the insertion (or deletion) atposition 18 of the variant amino add sequences is particularlyimportant in determining the differential cross-reactivity.To test this proposal, residue 18 was deleted in one erabutoxinusing sitedirected mutagenesis, and the biological propertiesof the resulting mutant were examined. We found that full antigenicitywas restored in the previously unrecognized variant. The implicationsof this finding are discussed.     

Study of an aramid surface reactivity: Modification with a cold plasma or an electron beam followed by a postgrafting reaction

Different modes of activation are described for a postgrafting reaction of acrylic acid on poly(p-phenylene terephthalamid) (PPTA)mitrogen plasma or electron-beam irradiation. Both lead to surface radical formation, and these species are able to initiate grafting. The Functionalization through amino group attachment is characteristic of plasma treatment. Degradation initiated by UV-visible emission of plasma is noticed, leading to the amide clivage. The surface grafting is more important when the PPTA is irradiated with a cold plasma and if water is used as the solvent. The polymer crystallinity degree reduces the grafting of the electron beam-irradiated PPTA even with a high radical concentration. © 1994 John Wiley & Sons, Inc.