Effect of acidification on elemental and isotopic compositions of sediment organic matter and macro‐invertebrate muscle tissues in food web research

Stable isotope techniques in food web studies often focus on organic carbon in food sources which are subsequently assimilated in the tissue of consumer organisms through diet. The presence of non‐dietary carbonates in bulk samples can affect their δ¹³C values, altering how their results are interpreted. Acidification of samples is a common practice to eliminate any inorganic carbon present prior to analysis. We examined the effects of pre‐analysis acidification on two size fractions of sediment organic matter (SOM) from marine and freshwater wetlands and pure muscle tissue of a common freshwater invertebrate (Cherax destructor). The elemental content and isotopic ratios of carbon and nitrogen were compared between paired samples of acidified and control treatments. Our results showed that acidification does not affect the elemental or isotopic values of freshwater SOM. In the marine environment acidification depleted the δ¹³C and δ¹⁵N values of the fine fraction of saltmarsh and δ¹⁵N values of mangrove fine SOM. Whilst acidification did not change the elemental content of invertebrate muscle tissue, the δ¹³C and δ¹⁵N values were affected. We recommend to researchers considering using acidification techniques on material prepared for stable isotope analysis that a formal assessment of the effect of acidification on their particular sample type should be undertaken. Further detailed investigation to understand the impact of acidification on elemental and isotopic values of organic matter and muscular tissues is required. Copyright © 2010 John Wiley & Sons, Ltd.     

Coloration of Spirooxazine in Various Organic Matrices under Plastic Flow at High Pressure

The behavior of 1,3,3-trimethylspiro[indoline-2,3′-2H-naphtho[2,1-b][1,4]oxazine under plastic deformation was studied on high-pressure Bridgman anvil-type apparatus at 0.5–4 GPa and room temperature.__________Translated from Zhurnal Prikladnoi Khimii, Vol. 78, No. 6, 2005, pp. 977–983.Original Russian Text Copyright © 2005 by Zhorin, Zelenetskii, Kiselev, Marevtsev, Shienok.     

Dissolved oxygen in the bottom water of the Sea of Japan as a sensitive alarm for global climate change

The Sea of Japan, a semi-closed marginal sea (greatest depth ∼3700 m) in the northwestern-most Pacific Ocean, has an independent, deep convection system, which is driven by the formation and the sinking of cool, saline surface water towards the bottom in severe winters. Continuous measurement of dissolved oxygen using highly precise versions of the Winkler titration method has revealed 8-10% decreases in the bottom concentration of oxygen (O₂) over the past 30 years. The temporal decrease in O₂ means an imbalance between the supply of O₂ from the surface and the in situ consumption of O₂ in decomposing organic matter, suggesting that the change in the deep convection pattern of the Sea of Japan is probably caused by global climate change to reduce winter cooling of surface seawater.     

Reactions of Organic Ions at Ambient Surfaces in a Solvent-Free Environment

Solvent-free ion/surface chemistry is studied at atmospheric pressure, specifically pyrylium cations, are reacted at ambient surfaces with organic amines to generate pyridinium ions. The dry reagent ions were generated by electrospraying a solution of the organic salt and passing the resulting electrosprayed droplets pneumatically through a heated metal drying tube. The dry ions were then passed through an electric field in air to separate the cations from anions and direct the cations onto a gold substrate coated with an amine. This nontraditional way of manipulating polyatomic ions has provided new chemical insights, for example, the surface reaction involving dry isolated 2,4,6-triphenylpyrylium cations and condensed solid-phase ethanolamine was found to produce the expected N-substituted pyridinium product ion via a pseudobase intermediate in a regiospecific fashion. In solution however, ethanolamine was observed to react through its N-centered and O-centered nucleophilic groups to generate two isomeric products via 2H-pyran intermediates. The O-centered nucleophile reacted less rapidly to give the minor product. The surface reaction product was characterized in situ by surface enhanced Raman spectroscopy, and ex situ using mass spectrometry and H/D exchange, and found to be chemically the same as the major pyridinium solution-phase reaction product.     

Homolytic Substitution at the Sulfur Atom as a Tool for Organic Synthesis

The use of intramolecular homolytic substitution at the sulfur atom by aryl and vinyl radicals, as an alternative to the use of alkyl halides, and chalcogenides as radical precursors in organic synthesis is reviewed.     

Voltammetric determination of food colorants using a polyallylamine modified tubular electrode in a multicommutated flow system

This work describes the construction of a polyallylamine modified tubular glassy carbon electrode and its application in the electroreduction of food azo colorants (tartrazine, sunset yellow and allura red) by square wave voltammetry. The electrode modification prevented the surface fouling and, simultaneously, enhanced the analytical signal intensity. The developed unit was coupled to a multicommutated flow system which, given the complexity of samples, was designed to allow the implementation of the standard additions method in an automatic way, using only one standard solution.The described method presented a linear range up to about 2.0 × 10⁻⁴ mol l⁻¹ for the referred colorants, with a detection limit of 1.8 × 10⁻⁶ mol l⁻¹ for tartrazine, 3.5 × 10⁻⁶ mol l⁻¹ for sunset yellow and 1.4 × 10⁻⁶ mol l⁻¹ for allura red. The method was applied in the analysis of these colorants in several food samples, and no statistically significant difference between the results obtained by the proposed and the comparative method (HPLC) was found, at a 95% confidence level. Repeatability in the analysis of samples (expressed in R.S.D.) was about 3% (n = 10).     

On the behavior of an oblate spheroidal hematite particle in a simple shear flow under a uniform magnetic field applied in the flow direction

We discuss the orientational properties of an oblate spheroidal hematite particle and also its influence on the rheological characteristics of a dilute suspension of these magnetic particles, by means of an analytical approach based on the orientational distribution function. A hematite particle with oblate spheroidal shape has an important characteristic; that is, it is magnetized in a direction normal to the particle axis. From the balance of the torques acting on a particle, we have developed the basic equation of the orientational distribution function. This basic equation has been numerically solved in order to investigate the dependence of the orientational distribution on the various factors. If both the magnetic field and the shear flow are weak, the particle does not exhibit specific directional characteristics. If the magnetic field is more dominant, the particle inclines such that the oblate surface is parallel to the magnetic field direction. If the shear flow becomes more dominant, the particle shows a sharper peak of the orientational distribution in the shear flow direction. The viscosity due to the magnetic torque increases and finally converges to a constant value as the magnetic field increases. In a sedimentation process under the gravitational field, the translational diffusion coefficient decreases with increasing magnetic field strength in the present case of the magnetic field direction.     

Destruction of Organic Compounds in a High-Frequency Discharge Plasma at Reduced Pressure

Plasma Chemistry and Plasma Processing - Conditions of the destruction of organic compounds in a hf discharge plasma at reduced pressure and parameters of this plasma type are determined. The...     

Chemiluminescence from singlet oxygen under laminar flow condition in a micro-channel

Singlet oxygen was generated by reaction of sodium hypochlorite and hydrogen peroxide in a micro-channel. The two reagent solutions were delivered into the micro-channel by syringe pumps, providing a laminar flow. Such a laminar flow forms a liquid–liquid interface instantly in a micro-channel, and then the interface collapses gradually through molecular diffusion with the residence times. The chemiluminescence from the singlet oxygen was emitted in the course of the collapse of the interface under laminar flow condition. The chemiluminescence intensity was observed continuously and stably in the micro-channel as long as the reagents were fed into the channel. We examined the features of the chemiluminescence emitted in the micro-channel by changing the flow rates of reagents and the detection points in the micro-channel. The data obtained were considered along with the residence times and diffusion lengths. We also examined the effects of antioxidants, such as sodium azide, histidine, nitroblue tetrazolium, and 2-propanol on the chemiluminescence intensity.     

Dramatic selectivity changes on carrier gas flow change in a series-coupled GC capillary tandem

We describe the polarity of selectivity of a GC separation system in terms of Retention Index data. In a series-coupled capillary system having stationary phases of differing polarity even slight (independent!) carrier gas flow changes in one part of the capillary series result in a dramatic change of selectivity. “Dramatic” is a relative term! Using a simple electronically controlled flow changing device we found retention index changes of several hundred units for polar test compounds such as phenols on a SE30/Carbowax tandem. This means: The classical theoretical model for understanding retention (and selectivity) in chromatography must be corrected. We propose a very simple approach involving addition of the expression RESIDENCE TIME to the chromatographic vocabulary. Instead of using flow resistors, one can just add a pressure regulator to the coupling point. A powerful analytical concept is now in easy reach.     

Linear-sweep voltammetry at a dropping mercury electrode in continuous flow systems

Linear-sweep voltammetry at a dropping mercury electrode is examined in flowing systems with parallel, opposite and normal mercury and fluid flow. The influence of fluid velocity (0–12 cm s^?1) on current and potential parameters of linear-sweep voltammograms is described. The ranges of fluid velocity in which current parameters are independent of flow, were determined by analysis of variance. It is shown that at certain sweep rates, the current does not depend on fluid velocity up to 12 cm s^?1.     

Temporal trends of deuterium excess in global precipitation and their environmental controls under a changing climate

Journal of Radioanalytical and Nuclear Chemistry - Sixty-three representative sites around the world were selected to analyze the long-term variability of deuterium excess (d-excess) and its...     

Reversible photoinduced change in molecular ordering of diarylethene derivatives at a solution-HOPG interface

A diarylethene-pyrene diad and a diarylethene-pyrene-diarylethene triad were synthesized to investigate the photoinduced two-dimensional ordering change at a solution-HOPG interface. The molecular arrangements were detected by STM. The different photochromic isomers showed different orderings reflecting the differences in their molecular structures. For the diarylethene-pyrene-diarylethene triad, a new ordering appeared upon irradiation with UV light and returned to the original ordering upon subsequent irradiation with visible light. The new arrangement was assigned to the ordering of the closed-closed isomers based on the images of the isolated open- and closed-isomers. The relationship between the nature of the two-dimensional ordering and the molecular structure is discussed.     

Synthesis of a three-member array of cycloadducts in a glass microchip under pressure driven flow

The synthesis of a series of cycloadduct products carried out in a glass microchip under pressure driven flow is presented. Initially, four different compounds were synthesized individually with conversions similar to those obtained in the corresponding batch macroscale reactions. Using identical experimental conditions for all four compounds, the results were highly predictable and reproducible, without the need for individual optimization. A multi-reaction experiment was then carried out in a single chip achieving the synthesis of a three-member array in a single run.     

The scaling behavior of a highly aggregated colloidal suspension microstructure and its change in shear flow

The nature of the network structure and the evolution of structural change in shear flow were investigated for metal particle dispersions in terms of fractal aggregation of colloidal particles. Polymer-stabilized metal particle inks were prepared via a polyvinyl chloride coating dispersed in solvent. The fractal dimension of 1.74 was calculated with the scaling model based on the power law relationship between the elastic modulus and volume fraction. This scaling behavior can be explained by considering the deformable network structure of soft materials. While the elastic property of the floc was dominant, the limit of linearity was found at the inter-floc link, which is relatively weak and brittle. The steady shear results reveal two mechanisms that contribute to the breakdown of the microstructure in metal particle inks at increasing shear rate. Scaling of steady shear viscosity shows that these mechanisms are related to both inter-floc interactions and the elasticity of the floc itself. Further, these results suggest that individual flocs deform with weak inter-floc interactions and rupture into smaller flocs or aggregates at high shear stress, which is associated with the increased shear rate.     

Normal stress and shear stress in a viscoelastic liquid under oscillatory shear flow

Normal stress and shear stress of concentrated polystyrene solutions in a chlorinated diphenyl were measured under steady flow and oscillatory shear flow in a Weissenberg rheogoniometer. The normal stress difference was observed to oscillate at double the frequency of the applied shear strain with amplitude proportional to the square of the applied amplitude, while the shear stress was found to oscillate at the same frequency with amplitude proportional to the applied amplitude. A theoretical relation between the displacement of the oscillatory normal stress difference from zero level and the dynamic modulus derived by Lodge and other investigators was confirmed experimentally, and the theoretical predictions of Coleman and Markovitz concerning the relation among steady-flow normal stress difference and dynamic modulus were also confirmed. However, the theoretical predictions of Lodge, of Spriggs, Huppler and Bird, and of Williams on the relation between the amplitude and phase of oscillatory normal stress and those of oscillatory shear stress did not agree with experimental results.