Detection and Discrimination of Conspecific Scents by the Anguid Slow-Worm Anguis fragilis

We tested the ability of male slow-worms, Anguis fragilis, a limbless anguid lizard with secretive, semifossorial habits, to detect chemical associated with conspecifics by using a T-maze in the laboratory. Male slow-worms discriminated conspecific male and female scent deposits. Males selected the arm with female scent, suggesting that scent deposits may be used to locate potential mates. Also, male slow-worms did not avoid the chemicals of other males, suggesting that they are not territorial. However, males discriminated their own scent from those of other males, and spent more time exploring the arm with other male scent, which suggests that scent marks may bear information that could be used in future intrasexual social contexts. We conclude that discrimination of conspecifics based on scents may be more widespread than previously expected among lizards inhabiting visually restricted environments.     

Evaluating the In Vitro Metabolism of Docosahexaenoic Acid in Sheep Rumen Fluid

Rumen metabolism (e.g., biohydrogenation) of dietary unsaturated fatty acids (FA) is one of the main reasons why ruminant fats tend to be highly saturated and contain many isomerized FA intermediates. The process by which long-chain (20- to 24-carbon FA) polyunsaturated FA (LC-PUFA) are metabolized by rumen bacteria is not as well understood as that of linoleic or linolenic acids. In order to better understand the fate of LC-PUFA in the rumen several concentrations of docosahexaenoic acid (DHA) were evaluated in in vitro batch incubations ranging from 100 to 1,500 μg per 6 mL of incubation volume using rumen fluid from sheep and incubated for 0, 1, 2, 3, and 6 h. From the results, it was shown that DHA was extensively metabolized at low (100 to 300 μg/6 mL incubation volume), but not at high level of inclusion (800 μg). At 300 μg of DHA most of the depleted DHA was recovered as LC-DHA metabolites within the first 6 h of incubation, and at the lowest levels (100 μg of incubation volume) further metabolism is apparent at 6 h. Using SP-2560 GC columns several LC-DHA metabolites were shown to elute after 24:0 and just past DHA, a region generally free of interfering FA. The present in vitro study would appear to be a useful method to evaluate the production of DHA metabolites in combination with its depletion.     

Hyperspectral data influenced by sample matrix: the importance of building relevant reference spectral libraries to map materials of interest

Hyperspectral imaging (HSI) and mapping are increasingly used for visualization and identification of nanoparticles (NPs) in a variety of matrices, including aqueous suspensions and biological samples. Reference spectral libraries (RSLs) contain hyperspectral data collected from materials of known composition and are used to detect the known materials in experimental samples through a one‐to‐one pixel “mapping” process. In some HSI studies, RSLs created from raw NPs were used to map NPs in experimental samples in a different matrix; for example, RSLs created from NPs in suspension to map NPs in biological tissue. Others have utilized RSLs created from NPs in the same matrix. However, few studies have systematically compared hyperspectral data as a function of the matrix in which the NPs are found and its impact on mapping results. The objective of this study is to compare RSLs created from metal oxide NPs in aqueous suspensions to RSLs created from the same NPs in rat tissues following in vivo inhalation exposure, and to investigate the differences in mapping that result from the use of each RSL. Results demonstrate that the spectral profiles of these NPs are matrix dependent: RSLs created from NPs in positive control tissues mapped to experimental tissues more appropriately than RSLs created from NPs in suspension. Aqueous suspension RSLs mapped 0‐602 out of 500,424 pixels per tissue image while tissue RSLs mapped 689‐18,435 pixels for the same images. This study underscores the need for appropriate positive controls for the creation of RSLs for mapping NPs in experimental samples.     

High temperature oxidation characteristics of Nb–10W–XCr alloys

The effect of Cr content on the microstructure and cyclic oxidation behavior of Nb–10W–XCr alloys with four different compositions has been investigated. Experiments were conducted in air at 900 °C and 1300 °C; the oxidation kinetics have been evaluated in terms of weight change per unit area with respect to exposure time. Alloy's microstructure consists of Nb solid solution phase regions surrounded by a network of NbCr₂ Laves phase. A trend of improvement in oxidation resistance with increase of the intermetallic phase is observed at 1300 °C and oxidation kinetics follow a parabolic behavior. At 900 °C, alloys with higher Cr content exhibit higher oxidation rates than alloys with lower Cr content. The oxidation products are a mixture of CrNbO₄, and Nb₂O₅ and the amount of each oxide present in the mixture is related to the intermetallic phase content. Results delineate the influence of microstructure and composition on the oxidation mechanisms of these alloys that represent a promising base for high-temperature intermetallic alloy development.     

Thermal aging of Pd/Pt/Rh automotive catalysts under a cycled oxidizing–reducing environment

Mono- and multi-metallic (bi- and tri-) Pt, Pd and Rh supported on cerium-promoted alumina (La Roche, SAS-1/16) catalysts were tested for activity as TWC, both fresh [G.C. Koltsakis, and A.M. Stamatelos, Progr. Energy Combust. Sci. 23 (1997) 1] and after accelerated aging. Aging consisted of a treatment at 900°C for 5 h during which an oxidizing (2.5% O₂, 10% H₂O, in N₂) and a reducing (5.0% CO, 10% H₂O, in N₂) feedstream were cycled at 0.017 Hz through the catalyst. Activity tests were carried out by increasing temperature from 100 to 600°C at 3°C min⁻¹, while two oxidizing and reducing (±0.5 A/F) feedstreams were alternately (1 Hz) fed through the reactor at 125 000 h⁻¹ (STP). Conversion was continuously analyzed. Light-off temperature, T₅₀, conversion at 500°C (normal running temperature), X₅₀₀, and the stoichiometric window (A/F from 14.13 to 15.13) for stationary feedstreams, were determined.     

Nitrous oxide emissions from an Uruguayan argiudoll under different tillage and rotation treatments

Lack of local data limits estimation of nitrous oxide (N₂O) emissions from different land uses of Uruguay. As a first step towards obtaining local information, we measured from August 2003 to September 2004 N₂O fluxes from a rotation-by-tillage experiment established in 1993 and from a nearby natural pasture (NP). Nitrous oxide emission rates were measured on an event-driven basis by using the closed chamber technique with six replicates per treatment. Fluxes varied considerably with time and the higher rates (more than 30 g N ha⁻¹ day⁻¹) were generally associated with periods of high soil water content, high temperature, and/or decreasing soil nitrate. We could not identify, however, any statistically significant correlation between flux and these variables. Throughout the evaluation period, fluxes from crops or cultivated pastures tended to be higher than those from NP, but the effects of tillage (no-till and conventional tillage) or rotation (continuous tillage and rotation with pasture) were not consistent. The application of 112 kg N ha⁻¹ to barley did not increase N₂O fluxes probably due to a high fertilizer use efficiency caused by the recommended three-split application and by the lack of rain during this period. The annual cumulative flows of different treatments compared well with those estimated using IPCC methodology, but the high spatial and temporal variability observed in this one-year study indicate that further research is needed to obtain reliable data on N₂O fluxes from agricultural soils of Uruguay.     

Aggregation of Alcohols Ethoxylates in n-Heptane

The solubility and aggregation process of polyethoxylated non-ionic surfactants, of general formula C _i H_2i+1–(O–CH₂–CH₂) _j –OH with i = 6, 8, 10 and j = 3–6 (C _i EO _j ), in heptane were studied. The aggregation of C _i EO _j surfactants in heptane was investigated by using methylene blue (MB) as an absorption probe. In solutions of MB in the presence of these surfactants in heptane, at concentrations larger than the re-dissolution concentration, the UV bands associated to free MB (A ₁) and MB–EO complex (A ₂) were detected. The ratio of these intensities A ₂/A ₁, was used to study the kinetics of the complex formation in pure surfactant. The value of A ₂/A ₁ depends on the surfactant structure and the media wherein MB is dissolved, being larger in the pure surfactant than in heptane solutions. These results are explained in terms of solvent effect and aggregate structures on the complex formation.

A method for disentangling β-Si3N4 seeds obtained by SHS

The manufacture of β-Si₃N₄ seeds by self-propagating high temperature synthesis (SHS) presents some advantages, such as the low production costs, compared to other preparation methods based on sintering of α-Si₃N₄ powders and subsequent leaching out of the glassy phase. However, SHS process produces seed clusters that must be disentangled before use as reinforcing particles. Different mechanical and chemical treatments were tried to achieve good seed dispersion, proving that a combined treatment based on a hot basic etching and a short time attrition milling gave almost agglomerate-free particles with adequate features for seeding use.     

High efficiency and reusability of iridium complexes adsorbed in montmorillonite clay on catalytic hydrogenation of imines

Heterogenised homogeneous catalytic hydrogenation of aldimines by removable and reusable immobilised iridium complexes on montmorillonite clay. This revised version was published online in July 2006 with corrections to the Cover Date.