Glass transition behavior of emulsion-polymerized polymer films containing a surface-active agent

The glass transition behavior of emulsion-polymerized poly(methyl methacrylate) and polystyrene films containing sodium laurylsulfate as emulsifier was studied by measurements of dynamic mechanical properties and thermal depolarization current. The film specimens of the emulsion-polymerized polymers were prepared by casting from their benzene solutions. The glass transition temperatures of the emulsion-polymerized films are higher than those of the bulk-polymerized films. The higher glass transition temperature of the emulsion-polymerized films is attributed to the colloidal properties of sodium laurylsulfate in the process of the film formation. The restriction of the molecular chains in the emulsion-polymerized films is attributed to the interaction between the hydrophobic groups of sodium laurylsulfate and the polymer molecules.     

Autoxidation of ethyl eicosapentaenoate and docosahexaenoate

The extent of oxidation of ethyl esters of eicosapentaenoic (EPA) and docosahexaenoic acids (DHA) was compared quantitatively with that of ethyl linoleate (Lo) and ethyl linolenate (Ln) by oxygen uptake and formation of conjugated diene, hydroperoxide and secondary oxidation products. EPA and DHA esters were oxidized rapidly even at 5 C in the dark after an induction period of 3–4 days, while the induction periods of Ln and Lo esters were 20 days and more than 60 days, respectively. Oxygen uptake of EPA and DHA esters after the induction period was 5.2 and 8.5 times faster than that of ethyl Ln, respectively. Hydroperoxides of EPA and DHA esters are much less stable than those of ethyl Lo. The peroxide value is not necessarily a good indication of oxidation in these polyenoic acids because a considerable amount of secondary products is formed at the early stage of oxidation. Polymers were found to be major secondary products in these polyenoic esters.     

Fritless packed columns for capillary electrochromatography: separation of uncharged compounds on hydrophobic hydrogels

A novel column is described that does not require frits to keep packing material within a capillary. A continuous bed is prepared in situ in aqueous solution by radical copolymerization of N-isopropylacrylamide and 2-acrylamido-2-methylpropanesulfonic acid (the resultant gel is denoted poly(AMPS-co-IPAAm). N,N'-Methylenebisacrylamide is used for cross-linking. On the application of an electrical field, electroosmotic flow (EOF) is developed in the bed along the capillary, where fluid propulsion would be otherwise difficult to achieve. The resultant EOF transports neutral compounds through the column without forcing the gel out of the capillary. Examination of the fluid motion in the continuous bed using a video microscope system and an image processor shows a relatively flat flow profile of EOF. The bed functions as the stationary phase for reversed-phase capillary electrochromatography (CEC). This new approach is an alternative to packed capillary columns which have been used previously in CEC. A high efficiency is obtained for a steroid which is separated on a 4.0% total monomer concentration (T), 10.0% degree of cross-linking (C), and 10.0% mole fraction of AMPS in the total monomer (S), poly(AMPS-co-IPAAm) column. A mixture of polyaromatic hydrocarbons is separated on a 6.9% T, 5.8% C, and 5.5% S poly(AMPS-co-IPAAm) column. The capacity factor of benzo[a]pyrene increases from 0.63 to 1.91 as the acetonitrile content in a Tris-boric acid buffer is decreased from 45 to 30% (v/v). The run-to-run RSD of analyte migration time is less than 0.73%, and the day-to-day RSD is acceptable. Potential benefits of this approach are also mentioned.     

Mapping evapotranspiration using MODIS and MM5 Four-Dimensional Data Assimilation

Evapotranspiration (ET), the sum of evaporation from soil and transpiration from vegetation, is of vital importance in the hydrologic cycle and must be taken into consideration in assessments of the water resources of any region. The MODerate resolution Imaging Spectroradiometer (MODIS) sensor offers a promising opportunity for estimating daily ET with a 1 km spatial resolution, but is hampered by frequent cloud contamination or data gaps from other factors. In this study, 1) a stand-alone ET model was applied and tested during clear or partial cloudy sky conditions using MODIS-based inputs of land surface and atmospheric data and 2) meteorological simulations by using Four-Dimensional Data Assimilation (FDDA) system between MODIS and the 5th Generation Meso-scale Meteorological Model (MM5) was used in cloudy conditions to facilitate continuous daily ET estimates. The MODIS ET algorithm modified from Mu et al. (2007) is based on the Penman-Monteith equation and was applied to predict ET at flux measurement sites. This algorithm considers both the effects of surface energy partitioning processes and environmental constraints on ET. We devised gap-filling approaches for MODIS aerosol and albedo data that were identified as bottlenecks to determine retrieval rates of insolation and ET. MODIS-derived input variables (i.e., meteorological variables and radiation components) for estimating ET showed a good agreement with flux tower observations at each site. The retrieval rate of MODIS ET doubled at four flux measurement sites after gap-filling with negligible compensation was undertaken for accuracy. In spite of the high accuracy of MODIS-derived input variables, MODIS ET showed meaningful errors at the four flux measurement sites. These errors were mainly associated with errors in the estimated canopy conductance. During clear sky conditions, MODIS was used to calculate ET, while the MODIS-MM5 FDDA system provided input variables for the calculation of ET under cloudy sky conditions. The performance of the MODIS-MM5 FDDA system was evaluated by comparing ET based on MODIS, which showed a good agreement with the MODIS ET for various land cover types. Our results indicate that MODIS can be applied to monitor the land surface energy budget and ET with reasonable accuracy and that MODIS-MM5 FDDA has the potential to provide reasonable input data of ET estimation under cloudy conditions.     

Dynamic alternation of primate response properties during trial-and-error knowledge updating

Humans and animals seek appropriate solutions to novel problems through trial-and-error (TE) actions and observation of their outcomes. Once an individual has obtained the knowledge (rule) to solve a problem, knowledge-based (KB) actions may be applied in a stereotypical manner. Solutions can thus be based on TE or KB actions. To characterize this learning process at the behavioral level, we developed a new cognitive task for a laboratory monkey (Macaca fuscata) to perform. In this task, a search array consisting of six elements of different colors was presented, one of which was the behaviorally relevant target. The target color was changed unpredictably with no instruction or signal, requiring the monkey to use a TE search strategy to find the target color. We found that once the monkey identified the relevant color by chance after a color change, correct performance increased in a step-like manner and at the same time, other response properties (reaction time and color-choice tendency) also changed discontinuously. These step-like alternations in behavioral performance may be attributed to the subject’s switching between TE and KB search strategies in the two phases. The present study has therefore provided behavioral evidence for the timing and manner of switching between search strategies during the process of updating knowledge.     

Electrochemical behaviour of pyridinoline, a crosslinking amino acid of collagen

Pyridinoline is a crosslinking amino acid isolated from collagen. Polarographic oxidation and reduction potentials of pyridinoline were measured and compared with those of structurally related compounds, 3-hydroxypyridine, pyridoxine, pyridoxal, and N-methylpyridoxine. Oxidation and reduction potentials of these compounds were found to be near anodic and cathodic limit potentials, respectively, except for pyridoxal. This indicates that a 3-hydroxypyridine ring is very difficult to be reduced or oxidized. The reducibility of pyridinoline with a reducing agent, sodium borohydride, was also studied. It was not reduced by the reagent, however, it was found to be decomposed by light during the treatment. These results indicate that pyridinoline is a so-called "non-reducible" crosslink.     

Numerical computation of two-loop box diagrams with masses

A new approach is presented to evaluate multi-loop integrals, which appear in the calculation of cross-sections in high-energy physics. It relies on a fully numerical method and is applicable to a wide class of integrals with various mass configurations. As an example, the computation of two-loop planar and non-planar box diagrams is shown. The results are confirmed by comparisons with other techniques, including the reduction method, and by a consistency check using the dispersion relation.     

Complete Photochemical Regulation of 8–17 DNAzyme Activity by Using Reversible DNA Photo-crosslinking

The regulation of DNAzyme activity is an important problem for its in vivo applications. We achieved photochemical regulation of DNAzyme activity by using reversible DNA photo-crosslinking of 3-cyanovinylcarbazole (^CNVK). The ODN containing ^CNVK photo-crosslinked to a pyrimidine base in the complementary strand after a few seconds of photoirradiation, and its photoadduct was split by photoirradiation of another wavelength. The activity of photo-crosslinked DNAzyme with ^CNVK was completely inhibited (OFF state). In contrast, after 312 nm irradiation, DNAzyme activity was recovered upon addition of a substrate strand (ON state). In addition, the photo-crosslinked DNAzyme is prone to enzymatic digestion by exonuclease. This photochemical OFF to ON switching with reversible DNA photo-crosslinking was regulated at the desired time and position; therefore, it might be possible to use it for in vivo application.