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Two experiments were conducted to evaluate the effect of amino acid (AA) injections in ovo in Cobb broiler breeder eggs on hatchability and subsequent chick BW. In Experiment 1, moisture, crude fat (CF), and CP were analyzed over time during incubation (Day 0, 7, 14, and 19 of incubation). Moisture, CP, and CF of the embryo increased, and moisture, CP, and CF of eggs decreased, as incubation time increased (P < 0.05). Combined egg and embryo AA contents, except Gly and Pro, decreased (P < 0.05) as incubation time increased. However, the pattern of AA in the egg did not change as the embryo developed. In Experiment 2, AA were injected into the yolk or air cell at Day 0 and 7 of incubation. Hatchability was reduced (P < 0.05) when AA were injected at Day 0 of incubation. However, when the AA solution was injected into the yolk sac at Day 7 of incubation, hatchability was not affected, and BW of chicks increased relative to egg weight prior to incubation. These results suggest that in ovo administration of AA may be an effective method of increasing chick BW at hatch.

Femtosecond time-resolved near-infrared spectra of TiO2 and Pt/TiO2 powders are measured at the wavelength region of 0.9−1.5 μm with the direct absorption method. Broad absorption bands of charge carriers, mainly free and trapped electrons, are observed for TiO2 and Pt/TiO2. The absorption band shape changes with a time constant of 160 fs after the photoirradiation, which most probably reflects the trapping of the generated free electrons. Population decay curves of the carriers after 1 ps, obtained for three different pump light powers, are well-explained by the second-order decay kinetics with a common second-order rate constant, indicating nongeminate recombination of the electron−hole pairs. When Pt is loaded to TiO2, an additional decaying process of 2.3 ps is observed. This decay component represents the transfer of generated electrons from TiO2 to Pt, which is consistent with the known increase of overall catalytic activities by the Pt cocatalyst.

Sulfur-doped TiO 2 was prepared by two methods; one was simple oxidation annealing of TiS 2 , the other was mixing of titanium isopropoxide and thiourea. These two sulfur-doped TiO 2 preparations showed fairly different photocatalytic activity under visible light. The dynamics of photogenerated charge carriers were studied by the transient absorption measurement in the region of mid-IR. In both samples, excitation by 532 nm pulse led to photocarrier generation to the same extent. Nevertheless, the reactivity of the photocarriers was totally different. Photogenerated electrons and holes transferred to reactant gas in the latter sample, whereas they did not in the former sample. We attributed the different carrier behavior to the difference in the distribution of S atoms or particle size. These observations can explain the difference in capability of photocatalysis under visible light.

We first demonstrated chiral vibrational sum frequency generation (VSFG) in the heterodyne detection, which enables us to uniquely determine chiral second-order nonlinear susceptibility consisting of phase and amplitude and distinguish molecular chirality with high sensitivity. Liquid limonene was measured to evaluate the heterodyne-detected chiral VSFG developed in this study. R-(+)- and S-(-)-limonene showed clearly opposite signs in the complex spectra of the second-order nonlinear susceptibility in the CH stretching region. This is the first report of the chiral distinction by VSFG without any a priori knowledge about chiral and achiral spectral response. Furthermore, from the phase of the chiral VSFG field measured in the heterodyne detection, the origin of the chiral signal was ascribed to the bulk limonene. The heterodyne detection also improves detection limits significantly, allowing us to observe weak chiral signals in reflection. The heterodyne-detected chiral VSFG can provide information on absolute molecular configuration.

Two experiments were conducted to evaluate the effect of in ovo amino acid (AA) injections in broiler breeder eggs on AA utilization of embryos. All AA used in these experiments were pure crystalline AA in free-base form. Treatments in Experiment 1 comprised 1) control eggs (no injection), 2) 0.5 mL sterile-distilled water injected eggs, and 3) eggs injected with an AA solution suspended in 0.5 mL sterile-distilled water. Injections were administered into the yolk at Day 7 of incubation. At hatch, chicks were killed and bled, and plasma AA concentration was determined. Plasma AA concentration of hatched chicks decreased (P < 0.05) when water was injected. In addition, all AA from eggs injected with AA, except Glu and Lys, were decreased (P < 0.05) at hatch as compared to control eggs. However, AA pattern was not affected by in ovo water injection, but the AA ratio to Lys was reduced by in ovo AA injection. Experiment 2 was conducted to evaluate whole internal egg AA concentrations over incubation time in the presence or absence of in ovo AA administration. Treatments in Experiment 2 comprised 1) control eggs (no injection), and 2) eggs injected with a AA solution at Day 7 of incubation. The AA contents of embryo, yolk, albumen, and allantoic and amnion fluids were analyzed over time during incubation (Days 0, 7, 14, and 19 of incubation). On Day 14 of incubation, there were no differences in AA contents of all tissues between the control group and the group injected with AA on Day 7 of incubation. On Day 19 of incubation, AA contents of embryo, yolk, albumen, and allantoic and amnion fluids were increased (P < 0.05) as mediated by in ovo administration of AA at Day 7 of incubation. These results suggest that in ovo administration of AA may increase AA concentrations in chicken embryos and other egg contents.

The reaction kinetics of electrons photoexcited in a Pt/TiO2 catalyst were observed by time-resolved infrared absorption in the presence of methanol−water vapor mixtures. The recombinative decay of the electrons was completed in microseconds on the catalyst exposed to a vacuum. The decay was suspended in the catalyst exposed to pure methanol vapor due to an effective hole-consuming reaction by adsorbed methoxy species. The suspension was released as partial water pressure was increased, indicating that the holes reacted with the methoxy species without the aid of adsorbed water or hydroxyl species. The excess electrons remaining in the catalyst were consumed by adsorbed water in a time domain of 0.1 s. The water-induced promotion of the methanol oxidation reaction described in the literature was interpreted with these results.