New species of Aeromonas isolated in Cuba

One hundred and fifty-five strains of Aeromonas isolated in the stools of children under 5 years presenting with acute diarrheal disease were studied. Using the Aerokey II system for the identification of species, 47 strains were identified as Aeromonas caviae, 58 as Aeromonas hydrophila, 23 as Aeromonas veronii biovar sobria, 14 as Aeromonas trota, 9 as Aeromonas veronii biovar veronii, 2 as Aeromonas jandaei and 2 as Aeromonas shubertii, Emphasis is placed on the advantages of this method which allowed for the classification of new species not identified previously in our country.     

Electrocatalysis of oxygen reduction on a carbon supported platinum-vanadium alloy in polymer electrolyte fuel cells

The electrocatalysis of the oxygen reduction reaction (ORR) on carbon supported Pt:V 1:1 catalyst in polymer electrolyte fuel cells (PEFC) was investigated. At an oxygen pressure of 1 atm results indicate a lower electrocatalytic activity for the ORR in the presence of vanadium. However, at an O₂ pressure ≥2 atm an enhanced electrocatalytic property of PtV/C compared with Pt/C is revealed. This result indicates the occurrence of a different electrocatalytic mechanism for the ORR on Pt/C and PtV/C. An increase of mass transport overpotentials is observed for the PtV/C catalyst, and this was related to the presence of vanadium oxide. Indeed, XRD analysis revealed that only about 30% of V present in the catalyst is alloyed with Pt, forming a face centred cubic (fcc) Pt₃V solid solution. A thermal treatment at 850 °C under reducing atmosphere leads to the formation of an ordered fcc Pt₂V phase. After this, the ORR activity of PtV/C at O₂ pressure 1 atm is higher than that of Pt/C.     

SELECTIVITY STUDIES IN THE PHOTOCHLORINATION OF METHANE II: EFFECT OF THE RADIATION SOURCE OUTPUT POWER AND OUTPUT SPECTRAL DISTRIBUTION

The effect of the output power and output spectral distribution of the radiation energy fed to a photoreactor upon the reaction yield and selectivities is studied both theoretically and experimentally. The study aims at the analysis of these influences in a series reaction such as the photochlorination of methane where methylene chloride and eventually chloroform are the most valuable products. The computational model employed has been verified for a group of selected conditions by means of bench-sale experiments.

It is found that the chlorine conversion shows the expected square root dependence with respect to the Local Volumetric Rate of Energy Absorption (LVREA). This dependence, in a first approximation, can also be assigned to the effect of the radiation source output power upon yield. It is also found that by manipulating the amount of radiation power fed to the reactor it is possible to ascertain the operating conditions favoring the production of predetermined intermediate products (e.g., methylene chloride or chloroform).

It is concluded that the use of customized lamps especially designed for each particular product on the basis of feasible changes in the characteristics of the existing radiation sources will favor a selective and more economical production of some of the stable intermediates, i.e., lamp design is an important feature in any optimal process design.     

Nitrous oxide emission from upland crops and crop-soil systems in northeastern China

Although it is known that crops can directly emit N₂O, their contribution to the total N₂O emission from crop-soil systems under field conditions is not well understood. This study was conducted to study the contribution of crops to total N₂O emission from soybean-soil and maize-soil systems in northeastern China. The effects of N fertilization on N₂O emission and NO ₃ ⁻ -N concentration in plants were also studied. The emission from crop-soil systems was measured with the closed chamber method, whereas the direct emission from crops was measured with the soil surface-sealed method. The addition of fertilizer N significantly increased the NO ₃ ⁻ -N concentration in crops and enhanced the N₂O emission from crop-soil systems and from crops alone. The amount of N₂O emitted directly from soybean plants accounted for 6 to 11% of the total soybean-soil emission. Similarly, the amount of N₂O emitted directly from maize plants accounted for 8.5 to 16% of the total maize-soil emission. The proportion of the applied N lost through direct N₂O emission from plants ranged from 0.19 to 0.34%, whereas the proportion of the applied N lost through N₂O emission from the crop-soil system ranged from 1.1 to1.9%. These results suggest that the use of chambers that do not include plants may lead to an underestimation of the total N₂O emission from crop-soil systems. This revised version was published online in November 2006 with corrections to the Cover Date.     

Agricultural use of three organic residues: effect on orange production and on properties of a soil of the ‘Comarca Costa de Huelva’ (SW Spain)

Disposal of urban, agricultural and industrial organic residues impliesan increasing problem because of all the economic and environmentalrepercussions involved. One of the most adequate ways of managing this problemis the agricultural use of these wastes as organic amendments. Three organicresidues (AC, olive mill waste water sludge compost; MWC, municipal solid wastecompost; and PS, paper mill sludge) were used in a 3-year field experimentinvolving orange production. The effect of their application on crop productionand on soil quality was investigated. Soil samples (0–20 cm depth)collected 11 months after the last soil amendment were analysed for: pH and EC,Kjeldahl-N, available-P, available-K, total organic carbon, humic substances,dehydrogenase, phosphatase, -glucosidase, urease andbenzoyl-argininamidehydrolysing protease (BAA-protease) activities. Generally, the application of the MWC and PSincreased orange yield when compared to control. Moreover, total organic carbonand humic substances significantly increased in soils treated with all theorganic amendments. Organic fertilisation increased the Kjeldahl-N andavailable-P contents of the soil. The application of the organic residues also causedsignificant increases in dehydrogenase, -glucosidase, urease andBAA-protease activities of the soil. Significant positive correlations (p <0.01) between these enzymatic activities and total organic carbon were foundforall treatments. Significant positive correlation between dehydrogenase, urease,-glucosidase, and BAA-protease and orange yield was also found. However,a clear inhibition of phosphatase activity was observed in soils treated withPS. The results indicate that the repeated application to the soil of moderateamounts of organic amendments has positive effects on the chemical andbiochemical properties of the soil, as well as on the orange yield.     

Predicting N mineralized in a Georgia Coastal Plain field

The N mineralized from soil organic matter provides an important portion of N available for crop production. The objective of this study was to determine the amount of spatial variability in N mineralization potential in a field and to evaluate three different methods that might be used to estimate this variability. The three methods tested included predicting the N mineralized from surface soil properties as well as from a biological and a chemical procedure. Three soils varying in N mineralization potential were selected for the study from a field in the Georgia Coastal Plain. The N mineralized from these soils was determined by an N balance of unfertilized and cropped plots. The amount of N mineralized could not be reliably predicted from surface soil organic C, although surface soil clay concentration was positively correlated with the N mineralized. The N mineralized that was predicted using mineralization parameters determined by aerobic incubation, adjusted daily for soil water content and temperature, was approximately 50% of the field measurements of N mineralized. The values of NH₄-N extracted with hot 2 M KCl were related significantly to N mineralized in the field (r²= 0.60) and also to the zero order rate constant of mineralization, k₀ (r²= 0.77), determined from the N mineralized in the aerobic laboratory incubation.     

Sex pheromone of tomato fruit borer, Neoleucinodes elegantalis

Five candidate pheromone components were identified by analyzing pheromone gland extracts by gas chromatography (GC), coupled GC-electroantennographic detection (EAD), and coupled GC-mass spectrometry (MS): (E)-11-hexadecenol(E11–16 : OH), (Z)-11-hexadecenol (Z11–16 : OH),(E)-11-hexadecenal, (E)-11-hexadecenyl acetate, and (Z)-3,(Z)-6,(Z)-9-tricosatriene (Z3,Z6,Z9–23 : Hy). In electroantennogram (EAG) recordings, synthetic E11–16 : OH elicited stronger antennal responses at low doses than other candidate pheromone components. Field tests demonstrated that synthetic E11–16 : OH as a trap bait was effective in attracting males, whereas addition of Z11–16 : OH inhibited the males' response. Z3,Z6,Z9–23 : Hy strongly enhanced attractiveness of E11–16 : OH, but was not attractive by itself. A pheromone blend with synergistic behavioral activity of an alcohol (E11–16 : OH) and hydrocarbon (Z3,Z6,Z9–23 : Hy) component is most unusual in the Lepidoptera. The synthetic two-component pheromone is approximately 60 times more attractive than the female-produced blend and might facilitate the control of this pest.     

Transesterification in poly(ethylene terephthalate) and poly(ethylene naphthalate 2,6-dicarboxylate) blends: model compounds study

Kinetics of transesterification reaction in poly(ethylene terephthalate)-poly(ethylene naphthalate 2,6-dicarboxylate), PET-PEN, blends resulting from melt processing was simulated using model compounds of ethylene dibenzoate (BEB) and ethylene dinaphthoate (NEN). The exchange reaction between BEB and NEN was followed by ¹H NMR spectroscopy using signals from the aliphatic protons of ethylene glycol moieties at 4.66 and 4.78 ppm, respectively. The first-order kinetics was established under pseudo-first-order conditions for both reactants. Thus, the overall transesterification reaction was second order reversible. The reversibility was confirmed experimentally by heating a mixed sequence of 1-benzoate 2-naphthoate ethylene (BEN) under similar conditions. Both forward reaction of the equimolar amounts of the reagents and reverse reaction came to equilibrium at the same molar ratio of the reactants and reaction products of roughly 0.25:0.50:0.25 for BEB, BEN, and NEN, respectively. The rate equation for the transesterification reaction in the model system was modified using half-concentration of BEN, which is the only effective in the intermolecular exchange. Direct ester-ester exchange was deduced as a prevailing mechanism for the transesterification reaction under the conditions studied, and the values of equilibrium and rate constants, as well as other basic thermodynamic and kinetic parameters were determined. The use of Zn(OAc)₂ as a catalyst resulted in a significant decrease in the activation enthalpy of transesterification, which might be due to the partial switch of the reaction mechanism from primarily pseudo-homolytic to more heterolytic where Zn^II acts as a Lewis base which binds to the ester carbonyl oxygen.     

Characterization and modeling of diffusion process for mass transport through the Tournemire argillites (Aveyron, France)

Argillites are one of the geological formations studied by IRSN for their confining properties for isolation of radioactive wastes. One of the main objectives is the study of water transport through rocks with very low water content and very low hydraulic conductivity by modeling of natural tracer profiles. This paper presents the protocol developed for and applied to the acquisition of data for chloride content in interstitial water of the Toarcian argillites at the Tournemire site (Southern France). This protocol is based on laboratory diffusion experiments and on modeling. Experimental data obtained during the transient and steady-state parts of diffusion experiments enable, respectively, the assessment of the diffusion coefficient and the determination of Cl concentration in pore water. Using this protocol, profiles with depth for both of these data sets have been acquired along the geological sequence. Taking into account the present knowledge of the geological and hydrogeological history of the Tournemire massif, a conceptual model granting the main role for mass transport to diffusion has been proposed. According to this conceptual model, a one-dimensional numerical model was built for simulating the mass transport of chloride through the sedimentary column, over 53 Ma. The good agreement between experimental data and calculated values for both diffusion coefficients and concentrations of chloride confirms that diffusion is likely the main process for mass transport in the massif. This model was also tested with the deuterium content of interstitial water, applying variable concentrations at the aquifer system boundaries for reflecting the thermal dependency of isotopic composition in precipitation. These simulations also reveal the likely important role of heterogeneities, such as fractures, in the variability of tracer concentrations with regards to a simple diffusion profile.     

Adapting the potentially mineralizable N concept for the prediction of fertilizer N requirements

Quantification of N dynamics in the ecosystem has taken on major significance in today's society, for economic and environmental reasons. A major fraction of the available N in soils is derived from the mineralization of organic matter. For decades, scientists have attempted to quantify the rate at which soils mineralize N, but the complexity of the N cycle has made this a major task. Further, agronomists have long sought soil test methods that are practical, yet will provide accurate means of predicting the amounts and rates of release of N from soils. Such tests would allow us to make more precise fertilization decisions. This paper discusses the potentially mineralizable N concept, first promoted by Stanford and colleagues [61, 62, 64], and suggests how it may be incorporated into deterministic models, such as CERES and LEACHM, so as to provide more accurate estimates of N mineralization under field conditions. We also suggest how the potentially mineralizable N concept may be coupled to quick, routine laboratory methods of determining available soil N, such as the hot 2M KCl extracted NH₄-N method recently developed by Gianello and Bremner [35], and used together with deterministic N models, such as CERES, for predicting probable fertilizer N requirements.