Present or Past Herbivory: A Screening of Volatiles Released from <Emphasis Type="Italic">Brassica rapa</Emphasis> Under Caterpillar Attacks as Attractants for the Solitary Parasitoid, <Emphasis Type="Italic">Cotesia vestalis</Emphasis>

Females of the solitary endoparasitoid Cotesia vestalis respond to a blend of volatile organic compounds (VOCs) released from plants infested with larvae of their host, the diamondback moth (Plutella xylostella), which is an important pest insect of cruciferous plants. We investigated the flight response of female parasitoids to the cruciferous plant Brassica rapa, using two-choice tests under laboratory conditions. The parasitoids were more attracted to plants that had been infested for at least 6 hr by the host larvae compared to intact plants, but they did not distinguish between plants infested for only 3 hr and intact plants. Although parasitoids preferred plants 1 and 2 days after herbivory (formerly infested plants) over intact plants they also preferred plants that had been infested for 24 hr over formerly infested plants. This suggests that parasitoids can distinguish between the VOC profiles of currently and formerly infested plants. We screened for differences in VOC emissions among the treatments and found that levels of benzyl cyanide and dimethyl trisulfide significantly decreased after removal of the host larvae, whereas terpenoids and their related compounds continued to be released at high levels. Benzyl cyanide and dimethyl trisulfide attracted parasitoids in a dose-dependent manner, whereas the other compounds were not attractive. These results suggest that nitrile and sulfide compounds temporarily released from plants under attack by host larvae are potentially more effective attractants for this parasitoid than other VOCs that are continuously released by host-damaged plants.     

In situ preparation of nano ZnO/hyperbranched polyimide hybrid film and their optical properties

Novel hybrid films of fluorinated hyperbranched polyimide (HBPI) and zinc oxide (ZnO) were prepared via the in situ sol-gel polymerization technique, in which mono-ethanolamine (MEA) was used as the coupling agent between the termini of HBPI and the precursor of ZnO. The hybrid films were characterized by transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) absorption, ultraviolet-visible (UV-vis) absorption, and fluorescent excitation/emission spectroscopy. The films, which originated from the colourless fluorinated HBPI structure and homogeneously dispersed ZnO nanoparticles, exhibited good optical transparency. Furthermore, two kinds of model compounds with and without ZnO and a HBPI film blended with ZnO microparticles were prepared to clarify the fluorescence mechanism in the pristine HBPI and in situ hybrid films. Efficient energy transfer from the ZnO nanoparticles to the aromatic HBPI main chains was observed in the in situ hybrid films, whereas energy transfer occurred only from the locally excited (LE) states to the charge-transfer (CT) state in the HBPI film. These facts demonstrate that the peripheral termini of HBPI are covalently bonded to ZnO particles via the MEA function, which operates as an effective pathway for energy transfer to give intense fluorescent emission.     

Phospholipid polymer hydrogel formed by the photodimerization of cinnamoyl groups in the polymer side chain

We synthesized new polymers with both photocrosslinkability and biocompatibility by a random copolymerization of 4‐(4‐methoxycinnamoyl)phenyl methacrylate and 2‐methacryloyloxyethyl phosphorylcholine. These polymers were used as prepolymers to make a hydrogel by photoirradiation. Gelation began with 5 s of photoirradiation and reached an equilibrium state after 360 s of photoirradiation. The absorption maximum at 347 nm, attributed to the cinnamoyl group, disappeared with the photoirradiation time. That is, dimerization between cinnamoyl groups in the polymer proceeded and formed a hydrogel. The equilibrium water concentration of the hydrogels was more than 90%. Moreover, we succeeded in making a microshape hydrogel on glass by photoirradiation through a photomask. The window shape of the photomask was transferred to the hydrogel that was formed. We concluded that these photocrosslinkable polymers could be useful in preparing microfluidic devices for separating or immobilizing biomolecules and cells. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 44–50, 2007     

Structure of a novel disulfide of 2-(N-acetylcysteinyl)amido-2-deoxy-alpha-D-glucopyranosyl-myo-inositol produced by Streptomyces sp

A novel dimer of an inositol glycoside was isolated from the mycelial extracts of Streptomyces sp. AJ 9463. Its structure was assigned as a disulfide of 2-(N-acetyl-L-cysteinyl)amido-2-deoxy-alpha-D-glucopyranosyl-(1-->1)-1D- myo- inositol (1).     

表面活性剂在气/液界面上扩散控制的吸附动力学(英文)

For the diffusion-controlled adsorption, the expression of dynamic surface adsorption P（t） was ob- tained by solving the diffusion equation. Two cases, i.e. the short and long time limits, were mainly discussed in this paper. From the measured dynamic surface tension of aqueous surfactant sodium dodecyl sulfate （SDS） solutions at 25 ℃, the adsorption kinetics of SDS at air/solution interface was studied. It was proved that for both of the short and long time limits, the adsorption process of SDS was controlled by diffusion.     

Dependence of vacancy concentration on morphology of helium bubbles in oxide ceramics

Since the formation of helium bubbles degrades swelling property and thermal conductivity of minor actinide-containing mixed oxide (MA-MOX) fuel, it is essential to understand the conditions of the bubble formation. In order to examine the dependence of vacancy concentration on morphology of helium bubbles, helium was infused into (Zr,Fe)O_2?x. The oxygen vacancy concentration was controlled by addition of solute Fe³⁺ into ZrO₂. Helium was infused by hot isostatic pressing. The helium-infused specimens were observed by field emission scanning electron microscopy (FE-SEM) and field emission transmission electron microscopy (FE-TEM). In addition, X-ray fluorescence, X-ray diffraction analysis, conversion electron yield–X-ray absorption near-edge structure and FE-SEM/EDX (energy dispersive X-ray) analyses were also made to interpret the results of microstructure observations. As a result of the helium infusion treatment, numerous 0.5–10 nm bubbles were observed and its number density clearly depended on oxygen vacancy concentration. On the other hand, sizes of the helium nano-bubbles in all specimens were almost constant.     

Ultra high-efficiency multi-photon emission blue phosphorescent OLEDs with external quantum efficiency exceeding 40%

We developed high-efficiency multi-photon emission (MPE) blue phosphorescent OLEDs with external quantum efficiency exceeding 40% at 100 cd m⁻². In these MPE devices, we used a blue phosphorescent emitter, FIrpic and pyridine-containing electron-transporters, B3PyPB and B3PyMPM, B4PyMPM. We also used a well-known electron-transporter, BCP for comparison. We used a combination of TAPC/MoO₃/Al/Liq layers as the charge-generation layer unit. An optimized MPE device showed an extremely high current efficiency of over 90 cd A⁻¹ and a high power efficiency of over 40 lm W⁻¹ at 100 cd m⁻² without any outcoupling enhancement.     

A BioDVD media with multilayered structure is suitable for analyzing biomolecular interactions

A biomolecular interactive analysis with antibody-antigen and aptamer-protein was evaluated on Au-over layers deposited on the BioDVD surface. BioDVD consists of multilayered structures with Au layer on the top and it detects analytes by monitoring the changes in reflected light intensity due to analyte adsorption to the sensor surface, on which functional biomolecules are immobilized to bind specifically to the analytes. The BioDVD sensing instrument is based on a commercial digital versatile disc system, which allows the instrument to be small and inexpensive. The BioDVD platform can be fabricated utilizing mass production techniques with additional functional phase change layers that can serve both to enhance sensitivity by optimization of the interferometric cavity optical properties and also as a possible medium for the storage of test related information.     

Rational Design of Double-Check Mercury Ion Chemosensors Based on Photochromic Compounds

A new photochromic compound, S1 , containing a trans-cis photoisomerizable unit and a mercury detecting chemosensor unit, has been designed and synthesized. S1 displayed dramatic selectivity for mercury ions over other ions, through fluorescence intensity measurement. In addition, in the photostationary state, a colorimetric response to mercury ions was also achieved. The fluorescence turn-off of S1 by mercury ions was defined as the first check, while mercury-induced colorimetric variation in the photostationary state was set as the second check. Thus, a double-check mercury chemosensor can be achieved.