Geochemical significance of the relative enrichment of pristane and the negative excursion of δ^13CPr across the Permian-Triassic Boundary at Meishan, China

Changes in the distribution of isoprenoid hydrocarbons and in δ^13Ckero or δ^13Cpr across the section from the Changxing Formation to the lower Yinkeng Formation at Meishan （the GSSP of PTB） are studied, in which a relative enrichment of pristane and a sharp shift in both δ^13Ckero and δ^13Cmole near the boundary are revealed. A possible mechanism for the abnormal accumulation of pristane near PTB is suggested： Lipids in some marine animals and their metabolites, rich in pristane, can be preserved and accumulate in some suitable depositing facies under certain special conditions, such as the catastrophic death of animals and/or developing of an anoxic water column, and thus the pristane enrichment occurs in the sediment. The occurrences of isoprenoid enrichment and high Pr/Ph ratios have been found in other typical marine anoxic sediments accompanied by mass extinction in various extent during the most important geological periods, such as Late Ordovician, end of Devonian, Early Jurassic and Late Cretaceous. These occurrences support to a certain extent the above mechanism that interprets the genesis of a high Pr/Ph ratio in some typical marine anoxic sediments. The synchronous sharp negative shifts in δ^13Cmole, δ^13Ckero and δ^13Ccarb from Beds 24 to 26 of the Meishan profile indicate that a sudden and strong variation of carbon source in the atmosphere-ocean system occurred during the quick but equable evolution from the end-Permian to Early Triassic, and the coupling between the pristane enrichment and negative shift in δ^13Ckero and δ^13CPr may well indicate the importance of the release of methane hydrates and marine anoxia in the end-Permian mass extinction.     

Flow-injection microcolumn on-line preconcentration for the determination of chromium (VI)

A rapid and sensitive on-line preconcentration method for spectrophotometric determination of chromium (VI) in nature water is described. Preconcentration and determination are based on (i) the quantitative and fast adsorption of chromium (VI) on the high surface area nanometer-size TiO₂ (anatase) powders, which prepared by a sol-gel method from hydrolysis of TiCl₄ and (ii) the quantitative and reproducible elution of Cr (VI) by 2.0 mol·L⁻¹ HCl. A mini-column system for preconcentration is developed, Cr(VI) on the mini-column is eluted and merged with a stream water and DPCB (1,5-diphenylcarbazide) as the chromogenic reagent. The proposed system permits throughputs of 6 sample h⁻¹ (0.001 μg·mL⁻¹ Cr(VI)) or 20 sample h⁻¹ (0.1 μg·mL⁻¹ Cr(VI)). The preconcentration factor is 55. The detection limit is 0.8 ng · mL⁻¹ Cr(VI). The reproducibility is satisfactory with a relative standard deviation of less than 3.35% (0.01 μg·mL⁻¹ Cr(VI),n=5). Supported by the National Natural Science Foundation of China Ma Wanhong: born in 1961, Ph. D. Graduate student, Associate professor     

Efficacy of anti-CD20 chimeric Fab’ fragment on proliferation of B lymphoma cells

The variable domain of heavy chain (V_H) and light chain (V_L) genes of anti-CD20 monoclonal antibody HI⁴⁷ were cloned from anti-CD20 ScFv expression vector pCANBTEcd20 by PCR and ligated into vector pYZF to construct chimeric anti-CD20 Fab’ fragment expression vector pYZFcd20. Chimeric anti-CD20 Fab’ fragment was expressed inE. coli 16C9 and purified by protein G affinity chromatography. Competitive inhibition assay showed that anti-CD20 Fab’ fragment inhibited binding of HI⁴⁷ to CD20 on the surface of Daudi cells. Results from MTT assay indicated that chimeric anti-CD20 Fab’ fragment inhibited the proliferation of Daudi cells, IC₅₀ = 69 μg/mL. Affinity of chimeric anti-CD20 Fab’ fragment was determined, K_a was about 8.9×10⁸ (mol/L)⁻¹.     

Multi-parameter infinite-dimensional (r,δ)-OU process

The definition of n-parameter infinite-dimensional (r,δ) -Ornstein-Uhlenbeck process {xt (·) } ((r, δ)-OUPn∞ for short) is given. The absolute continuity of distribution μt of Xt(·) and the limit of Xt(·) when |t| →∞ is discussed.     

3种苏铁属植物总黄酮、总多糖含量及抗氧化活性研究

为探究锈毛苏铁(Cycas ferruginea)、叉孢苏铁(C.segmentifida)和石山苏铁(C.sexseminifera) 3种苏铁属(Cycas)植物的总黄酮、总多糖含量以及抗氧化活性,本研究采用超声波辅助法对其根、叶柄、叶、雄球花、茎干的总黄酮及总多糖含量进行提取,以DPPH自由基(DPPH·)、羟自由基(·OH)、超氧阴离子自由基(O^-₂·)清除率评价其抗氧化活性,并采用Pearson相关性分析法分析相关性。结果表明：锈毛苏铁、叉孢苏铁和石山苏铁叶的总黄酮含量较高,大小依次为锈毛苏铁(8.61 mg·100 mg^-1)>叉孢苏铁(7.82 mg·100 mg^-1)>石山苏铁(1.04 mg·100 mg^-1);茎干中总多糖含量最高,大小依次为叉孢苏铁(28.32 mg·100 mg^-1)>石山苏铁(24.43 mg·100 mg^-1)>锈毛苏铁(16.59 mg·100 mg^-1<...     

Fluorescence Determination of Artemisinin Using Hemoglobin as Catalyst and Pyronine B as Substrate

0 IntroductionMaalnadria siusb atr ompajicosr .he aAltrthe pmrisoibnlienmi (n qtihneghtraoopsiucs,QHS,Fig.1) is a sesquiterpene endoperoxide isola-ted fromArtemisia annuaL., an ancient Chineseherbal medicine usedfor treatment of fever and ma-laria.Studies of the structure and activity relation-ship have shownthat endoperoxide groupis essentialfor anti malarial activity of QHS and absence of thismoiety lead to completely loss in activity of thedrug. Many techniques have been developed to de…     

Effect of Cl- on photosynthetic bicarbonate uptake in two cyanobacteria Microcystis aeruginosa and Synechocystis PCC6803

Photosynthetic inorganic carbon utilization was investigated in two cyanobacteria Microcystis aeruginosa and Synechocystis PCC6803 grown in standing culture. Photosynthetic rates for the two algae reached about 10 times the theoretical CO₂ supply rate at low dissolved inorganic carbon (DIC) of 100 μmol/L, and the rates were unaffected by the addition of 20 mmol/L Na⁺, indicating that the two algae possessed Na+-independent HCO^-₃ utilization for photosynthesis under low DIC. Their photo- synthetic rates at low DIC were inhibited by higher Cl^- and the degrees of inhibition were increased with the rise of CI^- concentration, and in the presence of Diphenylamine-2-carboxylate (DPC), a reported Cl^- channel inhibitor, the rates decreased by 74%－82%, implying that putative DPC-sensitive Cl^- channels participate in Na+-independent HCO₃^- uptake for photosynthesis. The experiment of intracellular 14C-DIC accumulation for photosynthesis showed that internal DIC pools decreased by about 80% with 200 μmol/L DPC and by 64%－70% with 100 mmol/L Cl^-. The experiment of chlorophyll a fluorescence quenching showed that initial rates and extents of fluorescence quenching obviously decreased with 200 μmol/L DPC or 100 mmol/L Cl^-. The two experiments gave further evidence that putative DPC-sen- sitive Cl^- channels participate in Na+-independent HCO^-₃ uptake for photosynthesis in the two algae grown in standing culture.     

An explanation to the high efficiency ofm-THPC (temporfin) used in photodynamic therapy

Meso-tetrahydroxylphenyl chlorin (m-THPC) is one of the most efficient prospective sensitizers used in photodynamic therapy (PDT). ESR spectroscopy, fluorescence quenching experiments and cyclic voltammogram measurement were used to study its redox properties. The results showed that the ability of m-THPC generating superoxide radical anions was very strong, and the rate constant of m-THPC fluorescence quenching by oxygen k_q (O₂)=1.46×10¹⁰ mol^-1·s^-1. The values of fluorescence quen- ching rate constant of m-THPC by some other electron acceptors, such as methyl viologen (MV²⁺) and anthraquinone (An), were also measured. And they were k_q (MV²⁺)=5.51×10⁹ mol^-1·s^-1, k_q (An)=7.81×10⁹ mol^-1·s^-1. The oxidation potential of m-THPC was examined to be +0.62 V (vs. NHE) in acetonitrile. All these suggested that m-THPC should be a much stronger electron donor than photofrin, the currently used in clinical photodrug, and may react easily through electron transfer with biological matter to yield various radicals. So it seemed reasonable that the type Ⅰ reaction may play an important role in the high activity of m-THPC-PDT.     

Responses of woody plant root and xylem sap ATP to soil drying

The ATP in roots and xylem sap of two woody plant species, Platycladus orientalis and Acacia auriculiformis, subjected to rapid and slow soil drying has been determined employing firefly luciferase ATP assay method (sensitivity is at 10-12 mol ATP L-1). The ATP levels in the two species were 1.6 nmol·gDW-1 and 0.6 nmol·gDW-1 in roots, and 5.6 μmol·m-3 and 8 μmol ·m-3 in xylem sap, respectively. When plants of P. orientalis and A. auriculiformis were subjected to rapid soil drying, respectively, as soil water content (SWC) decreased from the normal level ( 0. 25 g ·gDW-1) to 0. 02 and 0. 06 g ·gDW-1, separately, plant water potential ( ) dropped to -4 and -3.2 MPa, differently, the ATP in roots decreased 99.7% and 42%, respectively . When the rapidly dried soil was watered for up to 6 d, SWC and were found to recover to their normal levels, but ATP content in roots of P. orientalis and A. auriculiformis recovered by 10% and 23%, respectively. When plants of P. orientalis and A. auriculiformis were subjected to slow soil drying, respectively, as SWC was found to decrease from the normal level to 0.1 and 0.13 g·gDW-1, separately, dropped to - 2.5 and - 2 MPa, differently, the ATP content in roots decreased 98% and 38%, respectively. When the slowly dried soil was watered for up to 8 d, ATP levels in roots of P. orientalis and A, auriculiformis recovered by 30% and 24%, respectively. However, ATP concentrations in xylem sap were not directly influenced by either SWC or . The plot dots of xylem sap ATP concentration versus root ATP content were found to be distributed diagonally. It is concluded that ATP in roots is more sensitive in response to SWC changes than that to and root-sourced ATP is a source of that in xylem sap. When plants are subjected to slow soil drying, the ATP levels in both root and xylem sap are higher than that to rapid soil drying.     

Holocene vegetation cover in Qin’an area of western Chinese Loess Plateau revealed by n-alkane

Previous studies have found that wetlands prevailed in western Chinese Loess Plateau and pine pollen could reach up to 80% in Qin＇an area of the plateau during middle Holocene. It was then deduced that forest vegetation covered Qin＇an area in a warm and wet climate during middle Holocene. The proxies of molecule biomarkers from two Holocene sections, a swamp-alluvial loess section and a typical Ioess-paleosol section are used to reconstruct regional vegetation history. It is found that the heavy-molecular-weight （HMW） homologues of the n-alkanes in all samples exhibit a pronounced odd-over-even predominance, maximizing at C31 and the abundance of the nC27-alkanes is the lowest in nC27, nC29, nC31, i.e. C27〈C29〈C31, a typical grass n-alkanes model. The results are the same as those of model surface soil samples under grass cover but different from both forest cover and modern pine leaves, which yield preferentially nC29-alkanes peak. It could be inferred that the area was dominated by grass cover but not forest cover during whole Holocene epoch. The study shows that combining both molecule biomarkers and pollen analysis can avoid the disadvantage of pollen analysis in reconstruction of regional vegetation cover.     

Banach space valued martingales with respect to complex measure and their inequalities

Let dμ=ϕdν be a complex valued measure where ν is a non-negative measure and ϕ is a complex valued function which satisfiesb _p ⁺ orb _∞ ⁺ ⊂a ₁ condition. We prove some basic martingale inequalities such as B-G inequalities, weak (p, p) and strong (p, p) type inequalities for Banach space valued martingale with respect to complex measure μ. Supported by the National Natural Science Foundation of China Hou Youliang: born in 1956, Ph. D     

Kinetic studies of the decomposition reaction of adducts of dinuclear Fe(Ⅱ)/O2

Kinetic studies of the decomposition reaction of dinuclear Fe(Ⅱ) adducts [Fe₂(N-Et-HPTB){O₂P(OPh)₂}](Cl- O₄)₂ (1) and [Fe₂(N-Et-HPTB) {O₂P(Ph)₂}] (ClO₄)₂ (2) with O₂ have been carried out at low temperature using UV-vis spectra. The decomposition reaction of Fe(Ⅱ)/O₂ adducts was first-order in the experimental conditions, and the activation parameters were obtained. ?H^¹ = 85.62 kJ·mol^-1, ?S¹ = 19.43 J·mol^-1·K^-1 for compound (1) and ?H^¹ = 97.97 kJ·mol^-1, ?S^¹ = 55.68 J·mol^-1·K^-1 for compound (2). These results are similar to those of dioxygen adducts of other metals complexes and natural enzymes such as methane mono- oxygenase (MMOH).     

Effects of hydrolysis and bacterial degradation in the cells on hydrocarbons and biomarkers generated by pyrolysis of green algaChlorella protothecoides

The relative contents of normal alkanes and isoprenoid alkanes from pyrolysed pmducts of green algaChlorella protothecoides increased when the algal cell subject to hydrolysis and bacterial degradation were wed. Their value of C₂₃-/C ₂₄+ and the rate of Pr/C₁₇ increased greatly whereas the contents of C₂₀ alkenes were remarkably low compared with that from untreated sample (as control). These results are more analogous to the formation process of hydrocarbons derived from algae in natural geological environment.     

Microcalorimetric study on the antibiotic activity of clarithromycin and erythromycin

By using LKB-2277 Bioactivity Monitoring System, the heat effect changes in the process of inhibitory action of clarithromycin and erythromycin onEscherichia coli at 37°C were determined. Quantitative analysis showed that relationship between antibiotic concentrationc and rate contantk ofEscherichia coli growth, and half inhibitory ratio concentration IC₅₀: clarithromycin:k=0. 030 03–1. 1736×10⁻³ c, 8. 45 mg ·L⁻¹; erythromycin:k=0.031 08–8.4657×10⁻⁴ c, 14. 45 mg·L⁻¹. As a result of the microcalorimetry experiments, it not only indicated that antibacterial activity of clarithromycin was stronger than that of erythromycin, but also reported the changeable features of thermodynamics of the bacterial cell in biological, biochemical and metabolic process under different drug action. Foundation item: Supported by Natinal Natural Science Fundation of China (29973030), Natural Science Fundation of Hubei Province (98J052) and Post-doctoral Science Fundation of China Biography, SHEN Xue-song (1956-), Associate professor Research direction: biothermochemistry.     

Synthesis of layered LiMnO2 byin situ oxidation-intercalation and a study of the reaction mechanism and electrochemical performance

Using Mn(OH)₂ as precursor, LiOH as lithiating agent and (NH₄)₂S₂O₈ as oxidant, layeredo-LiMnO₂ was obtained by a novel method—in situ oxidation-intercalation under mild conditions (80 °C). The product was characterized by XRD, ICP, TEM and⁷Li-NMR. The results reveal that orthorhombic LiMnO₂ with high purity and good crystallinity can be obtained by this method. During electrochemical tests, a LiMnO₂/Li cell shows an initial reversible capacity of 208 mAh · g⁻¹ and a reversible capacity of 180 mAh · g⁻¹ after 30 cycles at room temperature.     

Effects of lithium chloride on outward potassium currents in acutely isolated hippocampal CA1 pyramidal neurons

Lithium is best known for its therapeutic efficacy in the treatment of manic-depressive illness. Its clinical profile includes the antimanic and antidepressant ac- tions as well as prophylaxis of both mania and depres- sion. Despite its efficacy, the mole…     

Sanitary Sewage Treatment with Jet Inner-loop Bioreactor

0　IntroductionThejetloopreactorhasthecharacteristicsofbothjetandloopflow .Ononehand ,theairsuckedinisdispersedintosmallgasbubblesbecauseoftheshearingforcecausedbythehighvelocityjet,producinganincreasedinterfacialcontactbe tweengasandliquid ,thusthemasstransferefficiencyisin creased .Ontheotherhand ,aregularloopflowisformedbecauseofmutualimpetusofbothjetandair lift,thusdramaticallyim provestheperformancesofmixture ,diffusion ,masstransferandheattransferofthematerial.Withoutmechanicdriving ,the…     

Effect of CO<Subscript>2</Subscript> concentrations on the activity of photosynthetic CO<Subscript>2</Subscript> fixation and extracelluar carbonic anhydrase in the marine diatom <Emphasis Type="Italic">Skeletonema costatum</Emphasis>

The growth and activity of photosynthetic CO2 uptake and extracellular carbonic anhydrase (CAext) of the marine diatom Skeletonema costatum were investigated while cultured at different levels of CO2 in order to see its physio-logical response to different CO2 concentrations under either a low (30 靘ol·m-2·s-1) or high (210 靘ol·m-2·s-1) irradiance. The changes in CO2 concentrations (4—31 靘ol/L) affected the growth and net photosynthesis to a greater extent under the low than under the high light re-gime. CAext was detected in the cells grown at 4 mol/L CO2 but not at 31 and 12 靘ol/L CO2, with its activity being about 2.5-fold higher at the high than at the low irradiance. Photo- synthetic CO2 affinity (1/ K1/2(CO2)) of the cells de-creased with increased CO2 concentrations in culture. The cells cultured under the high-light show significantly higher photosynthetic CO2 affinity than those grown at the low-light level. It is concluded that the regulations of CAext activity and photosynthetic CO2 affinity are dependent not only on CO2 concentration but also on light availability, and that the de-velopment of higher CAext activity and CO2 affinity under higher light level could sufficiently support the photosyn-thetic demand for CO2 even at low level of CO2.     

Modes of occurrence of arsenic in high-arsenic coal by extended X-ray absorption fine structure spectroscopy

The concentration ranges of As and Sb in six Late Permian high-arsenic coals collected from Xingren and Xingyi, Guizhou Province are 94.1 μg·g -1-3 2 and 8 1 μg·g -1-120 μg·g -1, respectively. Based on the mineralogical analysis, no arsenic and arsenic-bearing minerals are detected in these samples and arsenic occurs in coal macerals. By extended X-ray absorption fine structure(EXAFS) spectroscopy, we have found that arsenic in these high-arsenic coal samples coordinates with oxygen; the coordination number of As with oxygen for these samples is 4 except one sample(H-9) for which the coordination number of As is 3. Therefore, arsenic in these high-arsenic coals does not occur in sulfide minerals, but occurs in arsenate or arsenite phase, and the preponderance of As is in arsenate of As 5+.     

Crystallization kinetics of sea-salt aerosols studied by high-speed photography

Morphological changes with decreasing relative humidity(RH) of supersaturated sea-salt aerosol droplets on a quartz substrate were observed using a high-speed video-camera.Stable gypsum(CaSO4·2H2O) or the metastable hemihydrate(CaSO4·0.5H2O) were precipitated as the RH decreased.The dynamic process of crystal growth under steady-state humidity was studied by controlling the RH;the metastable hemihydrate was precipitated at 70.5%-77.1% RH,and the apparent crystal growth rate was between 1.42 and 2.33 μm3/s.Stable gypsum was formed at 80.7%-82.2% RH,and the apparent crystal growth rate was between 0.70 and 0.81 μm3/s.