The change of characteristics of tidal wave in the Changjiang River mouth area since the post-glacial transgression maximum

During the period of the post-glacial transgression maximum (PGTM), there was a huge trumpet estuary in the modern Changjiang River Delta area. The location and the shape of the Paleo-Changjiang River Estuary (PCRE) were much different from those of the present Changjiang River Estuary. The study on the change of characteristics of tidal wave in the Changjiang River mouth area since the PGTM can help to understand better the dynamic development of the Changjiang River Delta. The course curves of tidal level and tidal current velocity during a single tidal cycle for 35 points are calculated, and characteristics of tidal waves in the PCRE and its adjacent area are compared with those of tidal waves in the modern Changjiang River mouth area. The results show that the tidal waves within the PCRE and in its adjacent area during the period of the PGTM belonged to standing wave or a mixture of standing wave and progressive wave. Since then, the tidal wave in the Changjiang River mouth become gradually to be progressive wave with the PCRE being filled and the Changjiang River mouth shifting southeastwards.     

The change of characteristics of tidal wave in the Changjiang River mouth area since the post-glacial transgression maximum

During the period of the post-glacial transgression maximum (PGTM), there was a huge trumpet estuary in the modern Changjiang River Delta area. The location and the shape of the Paleo-Changjiang River Estuary (PCRE) were much different from those of the present Chang-Jiang River Estuary. The study on the change of characteristics of tidal wave in the Changjiang River mouth area since the PGTM can help to understand better the dynamic development of the Changjiang River Delta. The course curves of tidal level and tidal current velocity during a single tidal cycle for 35 points are calculated, and characteristics of tidal waves in the PCRE and its adjacent area are compared with those of tidal waves in the modern Changjiang River mouth area. The results show that the tidal waves within the PCRE and in its adjacent area during the period of the PGTM belonged to standing wave or a mixture of standing wave and progressive wave. Since then, the tidal wave in the Changjiang River mouth become gradually to be pr     

Fluid mud transportation at water wedge in the Changjiang Estuary

In situ data show that fluid mud of the Changjiang Estuary consists of fine sediment ranging from 8 to 11.5 μm (median grain-size) including 28.8%-36.4% of clay. The composition of the clay is illite, chlorite, kaolinite and montmoillonite. The FM is a layer of high sediment concentration near the bed and results from flocculation under the environment of salt and fresh water mixing. Three kinds of FM have been identified under typical dynamic conditions: the first one is formed at slack water of ebb tide during the flood season, with the characteristics of extended area and low thickness; the second one is formed following a storm, characterized by large area and larger thickness; the third one is formed around the front of the saltwater wedge, characterized by small area but large thickness. In the dredged channel, the FM can be accumulated up to 1 m thick. In general, FM will change with the alternation from spring to neap tides, flood and dry seasons. Drastic change can happen during storms. At the same time, the change of FM is closely related to the erosion and growth of the mouth bar.     

SIMULATION MODELLING OF THE IMPACTS OF SEA-LEVEL RISE SINCE THE LATEGLA-CIAL PERIOD ON THE CHANGJIANG(YANGTZE) RIVER, CHINA

Dramatic water stage rise and channel aggradation in the middle and lower reaches of the Changjiang (Yangtze) River have been recognized by previous studies. A further analysis of the data from geological, geomorphological, and paleohydrological surveys suggests that these changes might have resulted from sea-level rise since the Lateglacial period. So a mathematical model has been developed here, which reconstructs the processes of water-stage rise and channel aggradation of the Changjiang River as responses to sea-level rise since 12,100 a B.P.     

Element geochemistry of Holocene sediment and paleoenvironmental change in the Changjiang Estuary

Analyses of 41 elements reveal that Holocene sediments In the Changjiang Estuary bear regular elemental compositions in different sedimentary environments, and Holocene sediments came mainly from the Changjiang River based on compositions of REEs and most trace elements. Some heavy metals are more enriched in the surface sediment than in the deltaic sediments, reflecting human impact. Elemental compositions of the river channel sediment are related to the influence of proximal sediments. Sedimentary environments exert some influences on elemental compositions. Some chemical indices can be used to record chemical weathering undergone by the Changjiang sediment and environmental change.     

Element geochemistry of Holocene sediment and paleoenvironmental change in the Changjiang Estuary

Analyses of 41 elements reveal that Holocene sediments in the Changjiang Estuary bear regular elemental compositions in different sedimentary environments, and Holocene sediments came mainly from the Changjiang River based on compositions of REEs and most trace elements. Some heavy metals are more enriched in the surface sediment than in the deltaic sediments, reflecting human impact. Elemental compositions of the river channel sediment are related to the influence of proximal sediments. Sedimentary environments exert some influences on elemental compositions. Some chemical indices can be used to record chemical weathering undergone by the Changjiang sediment and environmental change.     

Field measurements of bottom boundary layer processes and sediment resuspension in the Changjiang Estuary

A field observation of the hydrodynamics and the sediment resuspension in a bottom boundary layer was carried out in the Changjiang Estuary, during July-August 1997. Using bottom field research facilities, detailed measurements of near-bottom currents and suspended sediment concentration distribution within 1.0 m above bed have been obtained in the Changjiang Estuary——a high concentration estuary. An Acoustic Suspended Sediment Monitor (ASSM) wasused to observe near bed sediment resuspension processes. In addition, the log-profile method was applied to estimating hydraulic roughness Z0 and bottom shear stress values (or friction velocities u). Further understanding of sediment suspension mechanics and hydrodynamic characteristics will require the long-term measurements of near bed processes.     

Spectroscopic study of association of a hemicyanine dye in mixed aqueous binary solvents

Electronic absorption and steady state emission properties of a hemicyanine dye [4-[4-(dimethylamino)styryl]-1-docosylpyridinium bromide], have been studied in several pure solvents and two mixed binary solvents (water+ethanol and water+acetonitrile). In pure solvents the band-width of the absorption spectrum correlates well with the Stoke's shift. In mixed aqueous solvents two different molecular forms of the solute, viz. the monomer and the dimer of the solute exists in equilibrium. Thermodynamic parameters (e.g. the Delta G degrees and Delta H degrees ) characterizing the equilibrium have been determined. While the value of Delta G degrees changes very slightly with the composition of the binary mixture, the value of Delta H degrees has been observed to depend significantly with solvent composition.     

A suite of novel allenes from Australian melolonthine scarab beetles. Structure,synthesis, and stereochemistry

A suite of allenic hydrocarbons, previously unknown as a molecular class from insects, has been characterized from several Australian melolonthine scarab beetles. The allenes are represented by the formula CH(3)(CH(2))(n)()CH=*=CH(CH(2))(7)CH(3) with n being 11-15, 17 and 19, and thus, all have Delta(9,10)-unsaturation. These structures have been confirmed by syntheses and comparisons of spectral and chromatographic properties with those of the natural components. The enantiomers of (+/-)-Delta(9.10)-tricosadiene and Delta(9,10)-pentacosadiene were separable on a modified beta-cyclodextrin column (gas chromatography), and the natural Delta(9,10)-tricosadiene (n = 11) and Delta(9,10)-pentacosadiene (n = 13) were shown to be of >85% ee. Syntheses of nonracemic allenes of known predominating chirality were acquired using both organotin chemistry and sulfonylhydrazine intermediates, and comparisons then demonstrated that the natural allenes were predominantly (R)-configured.     

Calculation of the relative acidities and oxidation potentials of para-substituted phenols. A model for alpha-tocopherol in solution

Relative acidities (Delta pK(a)) of phenols and oxidation potentials (Delta E(ox)) of the phenoxide anions have been calculated for nine para-substituted phenols using density functional theory. Solvent effects were incorporated using the conductor-like polarisable continuum method. Using the calculated Delta pK(a) and Delta E(ox) values in a thermodynamic cycle, the DeltaBDE (bond dissociation enthalpy) of the phenols were also determined with all values calculated to within 1.5 kcal mol(-1) of experiment. The Delta pK(a) and Delta E(ox) values were calculated for 6-hydroxy-2,2,5,7,8-pentamethylchroman (HPMC), a model for alpha-tocopherol for which there are no known experimental values. The acidity of this compound is raised by 2.4 pK(a) units and lowered by -0.79 V relative to phenol with a calculated Delta BDE of -14.9 kcal mol(-1). There is a negative correlation (r(2) = 0.86) between the Delta pK(a) and the Delta BDE values. A stronger and positive correlation is found between the Delta E(ox) (r(2) = 0.98) and the Delta BDE values. Using these correlations it is uncovered that hydrogen abstraction of phenols, as measured by the Delta BDE, is driven by electron transfer rather than by proton transfer.     

Estimation of dissolved inorganic nutrients fluxes from the Changjiang River into estuary

Because the estuary acts as either a trap or a source or both for nutrient elements and will modify greatly the riverine transport to the ocean, it is necessary to calculate the flux from river into estuary and that from estuary into sea, respectively. The present work aims to use a long-term record of nutrients concentrations and runoff discharges on H.e Datong section (625 km inland from the Changjiang River mouth) to identify the variability of nutrients concentrations and to estimate nutrients fluxes from the Changjiang River into the estuary.     

Estimation of dissolved inorganic nutrients fluxes from the Changjiang River into estuary

Because the estuary acts as either a trap or a source or both for nutrient elements and will modify greatly the riverine transport to the ocean, it is necessary to calculate the flux from river into estuary and that from estuary into sea, respectively. The present work aims to use a long-term record of nutrients concentrations and runoff discharges on H.e Datong section (625 km inland from the Changjiang River mouth) to identify the variability of nutrients concentrations and to estimate nutrients fluxes from the Changjiang River into the estuary.     

Thermodynamic study of adsorption of homologous anionic and cationic surfactants

The simplified form of an integral adsorption isotherm based on Butler's equation was applied to describe surface behavior of a series of anionic (sodium alkylsulfonates) and cationic (alkylpyridinium halides) surfactants. This theory allows for the calculation of the free energy of adsorption (Delta G jk) value corresponding to the ability of a particular surfactant to undergo adsorption. The obtained results indicate that the value of Delta G jk depends linearly on the length of the hydrocarbon chain as well as on the kind and concentration of the added inorganic electrolyte. Moreover, it has been found that in the case of surfactants, which have the same length of the alkyl chain and adsorb from solutions containing the same inorganic electrolyte, the charge of hydrophilic group has insignificant influence on the value of Delta G jk.     

Determination of the cis-trans isomerization barrier of enalaprilat by dynamic capillary electrophoresis and computer simulation

Dynamic capillary electrophoresis (DCE) and computer simulation of the elution profiles with the stochastic model has been applied to determine the isomerization barriers of the angiotensin converting enzyme inhibitor enalaprilat. The separation of the rotational cis-trans isomeric drug has been performed in an aqueous 20 mM borate buffer at pH 9.3. Interconversion profiles featuring plateau formation and peak broadening were observed. To evaluate the rate constants k(cis-->trans) and k(trans-->cis) of the cis-trans isomerization from the experimental electropherograms obtained by dynamic capillary electrophoresis, elution profiles were analyzed by a simulation with iterative convergence to the experimental data using the ChromWin software which requires the total migration times of the individual isomers t(R), the electroosmotic break-through time t(0), the plateau height h(plateau), the peak widths at half height of the individual isomers w(h), as well as the peak ratio of the isomers as experimental data input. From temperature-dependent measurements between 0 degrees and 15 degrees C the thermodynamic parameters Delta G, Delta H and Delta S, the rate constants k(cis-->trans) and k(trans-->cis) and the kinetic activation parameters Delta G*, Delta H*, and Delta S* of the cis-trans isomerization of enalaprilat were obtained. From the activation parameters the isomerization barriers at 37 degrees C were calculated to be Delta G* (trans-->cis) = 87.2 kJ.mol(-1) and Delta G*(cis-->trans) = 91.9 kJ.mol(-1).     

The permanent electric dipole moments of iron monoxide, FeO

The Q(4) and R(4) branch features of the (0,0)D (5)Delta(4)-X (5)Delta(4) band system and the Q(3) and R(3) branch features of the (0,0)D (5)Delta(3)-X (5)Delta(3) band system of iron monoxide FeO have been studied by optical Stark spectroscopy. The Stark splittings in the high resolution laser induced fluorescence spectra were analyzed to produce values for the magnitude of the permanent electric dipole moments /mu/ of 4.50+/-0.03, 4.29+/-0.05, 2.53+/-0.04, and 2.58+/-0.06 D for the X (5)Delta(4) (nu=0), X (5)Delta(3) (nu=0), D (5)Delta(4) (nu=0), and D (5)Delta(3) (nu=0) states, respectively. The results are compared to several ab initio predictions and to FeC. The qualitative trends are explained in terms of a molecular orbital correlation picture.     

Multielectron chemistry of zinc porphyrinogen: a ligand-based platform for two-electron mixed valency

The synthesis, electronic structure, and oxidation-reduction chemistry of a homologous series of Zn(II) porphyrinogens are presented. The fully reduced member of the series, [LZn](2-), was prepared in two steps from pyrrole and acetone. The compound undergoes consecutive two-electron, ligand-based, oxidations at +0.21 and +0.63 V vs NHE to yield [L(Delta)Zn] and [L(Delta Delta)Zn](2+), which also have been independently prepared by chemical means. X-ray diffraction analysis of the redox intermediary, [L(Delta)Zn], shows that the partly oxidized macrocycle is composed of a methylene-bridged dipyrrole that is doubly strapped to a two-electron oxidized dipyrrole bridged by a cyclopropane ring (L(Delta)). The localization of two hole equivalents on the oxidized side of the porphyrinogen framework is consistent with a two-electron mixed valency formulation for the [L(Delta)Zn] species. Electronic structure calculations and electronic spectroscopy support this formalism. Density functional theory computations identify the HOMO to be localized on the reduced half of the macrocycle and the LUMO to be localized on its oxidized half. As implicated by the energy level diagram, the lowest energy transition in the absorption spectrum of [L(Delta)Zn] exhibits charge-transfer character. Taken together, these results establish the viability of using a ligand framework as a two- and four-electron/hole reservoir in the design of multielectron redox schemes.     

Observation and calculation of the Cs2 2 3Delta(1g) and b 3Pi(0u) states

The Cs(2) 2 (3)Delta(1g) and b (3)Pi(0u) states have been observed by infrared-infrared double resonance spectroscopy for the first time. 221 2 (3)Delta(1g)<--A (1)Sigma(u) (+)<--X (1)Sigma(g) (+) double resonance lines have been assigned to transitions into the 2 (3)Delta(1g) v=6-13 vibrational levels. Resolved fluorescence into the b (3)Pi(0u) v(')=0-48 levels has been recorded. Molecular constants and potential energy curves are determined by the global fit of the entire set of the experimental data. Theoretical potential energy curves of the 2 (3)Delta(g) and b (3)Pi(u) states have been determined in the framework of the pseudopotential method and are compared with the experimental results.     

Heavy metal content of stormwater runoff in St. Petersburg

A procedure has been developed for the prediction of heavy metal concentrations in storm rainfall in St. Petersburg on the assumption of equal rates of metal influx with precipitations to the Baltic Sea and St. Petersburg territory. The concentrations of mercury, copper, and zinc in stormwater runoff from different administrative districts of the city have been calculated, and the predicted values have been compared with those determined experimentally.     

High-performance liquid chromatography-atmospheric pressure chemical ionization mass spectrometry and gas chromatography-flame ionization detection characterization of Delta5-polyenoic fatty acids in triacylglycerols from conifer seed oils

Edible conifer seeds can serve as a source of triacylglycerols (TGs) with unusual Delta5 unsaturated polymethylene interrupted fatty acids (UPIFAs), such as cis-5,9-octadecadienoic (taxoleic), cis-5,9,12-octadecatrienoic (pinolenic), cis-5,11-eicosadienoic (keteleeronic) and cis-5,11,14-eicosatrienoic acids (sciadonic). Conifer seed oils from European Larch (Larix decidua), Norway Spruce (Picea abies) and European Silver Fir (Abies alba) have been analyzed by non-aqueous reversed-phase high-performance liquid chromatography (NARP-HPLC) with atmospheric pressure chemical ionisation (APCI)-MS detection. The influence of different positions of double bonds in Delta5-UPIFAs on the retention and fragmentation behavior is described and used for the successful identification of TGs in each oil. TGs containing Delta5-UPIFAs have a higher retention in comparison with common TGs found in plant oils with single methylene interrupted Delta6(9)-FAs and also significantly changed relative abundances of fragment ions in APCI mass spectra. Results obtained from HPLC/MS analyses are supported by validated GC/FID analyses of fatty acid methyl esters after the transesterification. The total content of Delta5-UPIFAs is about 32% for European Larch, 27% for Norway Spruce and 20% for European Silver Fir. In total, 20 FAs with acyl chain lengths from 16 to 24 carbon atoms and from 0 to 3 double bonds have been identified in 64 triacylglycerols from 3 conifer seed oils.     

用Delta—Bar—Delta规则神经网络对肺癌患者的判别

采用Ｄｅｌｔａ规则和Ｄｅｌｔａ－Ｂａｒ－Ｄｅｌｔａ规则的神经网络，用于根据头发和血清样品中金属含量对正常人与癌症患者的分类判别研究，对有关参数影响作了讨论，结果表明，采用Ｄｅｌｔａ－Ｂａｒ－Ｄｅｌｔａ规则的神经网络训练速度明显快于Ｄｅｌｔａ规则的神经网络。