Prevalence and risk factors of subsyndromal delirium among postoperative patients: A systematic review and meta-analysis.

AIM: The aim of this study is to determine the prevalence and risk factors for subsyndromal delirium in the postoperative patient. DESIGN: A systematic review and meta-analysis. METHODS: The Review Manager 5.3 statistics platform and the Newcastle-Ottawa Scale were used for quality evaluation. DATA SOURCES: The following databases were searched: PubMed, Web of Science, EMBASE, The Cochrane Library, Scopus and EBSCO from January 2000 to December 2021. Additional sources were found by looking at relevant articles' citations. RESULTS: A total of 1744 titles were originally identified, and five studies including 962 patients were included in the systematic review, with a pooled prevalence of postoperative subsyndromal delirium (PSSD) of 30% (95% CI: 0.28-0.32). Significant risk variables for PSSD were older age, low levels of education (≤9 years), cognitive impairment, higher comorbidity score, and the duration of operation. CONCLUSION: PSSD is prevalent and is associated with a variety of risk factors as well as low academic performance. IMPACT: Identification and clinical management of patients with PSSD should be improved. Future research on PSSD risk factors should look at a wider range of intraoperative and postoperative risk factors that can be changed. PATIENT AND PUBLIC CONTRIBUTION: No Patient or Public Contribution.

Anion-Counterion Strategy toward Organic Cocrystal Engineering for Near-Infrared Photothermal Conversion and Solar-Driven Water Evaporation.

An anion-counterion strategy is proposed to construct organic mono-radical charge-transfer cocrystals for near-infrared photothermal conversion and solar-driven water evaporation. Ionic compounds with halogen anions as the counterions serve as electron donors, providing the necessary electrons for efficient charge transfer with unchanged skeleton atoms and structures as well as the broad red-shifted absorption (200-2000 nm) and unprecedented photothermal conversion efficiency (~90.5 %@808 nm) for the cocrystals. Based on these cocrystals, an excellent solar-driven interfacial water evaporation rate up to 6.1±1.1 kg ⋅ m-2 ⋅ h-1 under 1 sun is recorded due to the comprehensive evaporation effect from the cocrystal loading in polyurethane foams and chimney addition, such performance is superior to the reported results on charge-transfer cocrystals or other materials for solar-driven interfacial evaporation. This prototype exhibits the great potential of cocrystals prepared by the one-step mechanochemistry method in practical large-scale seawater desalination applications.

Ultrafast excited-state energy dissipation pathway of diethylamino hydroxybenzoyl hexyl benzoate (DHHB) via the nanoparticles.

The organic UVA filter is popularized in sunscreen cosmetics due to the advantages of excellent light stability and high molar extinction coefficient. However, the poor water solubility of organic UV filters has been a common problem. Given that nanoparticles (NPs) can significantly improve the water solubility of organic chemicals. Meanwhile, the excited-state relaxation pathways of NPs might differ from their solution. Here, the NPs of diethylamino hydroxybenzoyl hexyl benzoate (DHHB), a popular organic UVA filter, were prepared by an advanced ultrasonic micro-flow reactor. The surfactant (sodium dodecyl sulfate) was selected as an effective stabilizer to prevent the self-aggregation of the NPs for DHHB. Femtosecond transient ultrafast spectroscopy (fs-TA) and theoretical calculations were utilized to trace and explain the excited-state evolution of DHHB in NPs suspension and its solution. The results reveal that the surfactant-stabilized NPs of DHHB reserve a similarly good performance of ultrafast excited-state relaxation. The stability characterization experiments demonstrate that the strategy of surfactant-stabilized NPs for sunscreen chemicals can maintain its stability and enhance the water solubility of DHHB compared with that of the solution phase. Therefore, the surfactant-stabilized NPs of organic UV filters are an effective method to improve water solubility and keep the stability from aggregation and photoexcitation.

The Transport of Charged Molecules across Three Lipid Membranes Investigated with Second Harmonic Generation.

Subtle variations in the structure and composition of lipid membranes can have a profound impact on their transport of functional molecules and relevant cell functions. Here, we present a comparison of the permeability of bilayers composed of three lipids: cardiolipin, DOPG (1,2-dioleoyl-sn-glycero-3-phospho-(1'-rac-glycerol), and POPG (1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1'-rac-glycerol)). The adsorption and cross-membrane transport of a charged molecule, D289 (4-(4-diethylaminostyry)-1-methyl-pyridinium iodide), on vesicles composed of the three lipids were monitored by second harmonic generation (SHG) scattering from the vesicle surface. It is revealed that structural mismatching between the saturated and unsaturated alkane chains in POPG leads to relatively loose packing structure in the lipid bilayers, thus providing better permeability compared to unsaturated lipid bilayers (DOPG). This mismatching also weakens the efficiency of cholesterol in rigidifying the lipid bilayers. It is also revealed that the bilayer structure is somewhat disturbed by the surface curvature in small unilamellar vesicles (SUVs) composed of POPG and the conical structured cardiolipin. Such subtle information on the relationship between the lipid structure and the molecular transport capability of the bilayers may provide clues for drug development and other medical and biological studies.

Understanding the different cross-membrane transport kinetics of two charged molecules on the DOPG lipid surface with second harmonic generation and MD simulation.

A clear physical picture of the dynamic behavior of molecules on the surface of the lipid membrane is highly desired and has attracted great attention from researchers. In this study, a step forward in this direction based on previous studies was presented with second harmonic generation (SHG) and molecular dynamic (MD) simulation. Specifically, details on the orientation flipping and cross-membrane transport of two charged molecules, 4-(4-diethylaminostyry)-1-methyl-pyridinium iodide (D289) and malachite green (MG), on the surface of 2-dioleoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt (DOPG) lipids were presented. Firstly, the orientation flipping of the two molecules on the surface of lipids before their cross-membrane transport was confirmed by the MD simulation. Then, the concentration dependent rate of the cross membrane transport for MG/D289 was analyzed. It was found that a simplified model could satisfactorily interpret the faster cross-membrane transport of MG under higher bulk concentrations. A different concentration dependent dynamics was observed with D289 and the reason behind it was also discussed. With this investigation, the surface structures and dynamics of D289 and MG on the DOPG lipid surface were clearly presented.

Revealing the mechanisms of vesicle formation with multiple spectral methods.

The investigation of the self-assembly of amphiphilic molecules and the formation of micelles/vesicles has attracted significant attention. However, in situ and real-time methods for such studies are rare. Here, a surface-sensitive second harmonic generation (SHG) technique was applied to study the formation of vesicles in solutions of an anti-cancer drug, doxorubicin (DOX), and a generally used surfactant (sodium bis (2-ethylhexyl) sulfosuccinate, AOT). With the aid of two-photon fluorescence (TPF), Rayleigh scattering and TEM, we revealed the structural evolution of the aggregated micelles/vesicles. It was found that AOT and DOX molecules rapidly aggregated and formed micelles in the solution. The residual DOX then acted as a "glue" that induced the aggregating/growing of the micelles and the transformation from aggregates to vesicles. The existence of lipid films, which was considered as the necessary intermediate state for vesicle formation, was excluded via the SHG observations, indicating that hollow shells may be directly transformed from solid aggregated micelles in the self-assembly formation of complex vesicles. The combined spectroscopic methods were also used to investigate the formation of vesicles from a commonly used lipid (i.e., 1,2-dioleoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt, DOPG) from its stacked bilayers. The swelling, curving and sealing of the DOPG bilayers for vesicle formation was monitored and clear dynamics were revealed. This work shows that the vesicle formation mechanism varies with the initial state of the surfactant/lipid molecules. It not only demonstrates the capability of the combined spectroscopic methods in investigating the aggregated systems but also provides new insight for understanding the formation of vesicles.

Probing catalytic reduction on the surface of Au nanoparticles by second-harmonic generation and two-photon luminescence.

The catalytic reduction of aromatic nitro compounds by metallic nanoparticles in the presence of sodium borohydride (NaBH4) has been widely studied as model reactions. However, the reaction mechanisms still need further investigations. For example, the origin of the induction time that has often been observed is still controversial. Here, we demonstrated that such catalytic reduction reactions on the surface of colloidal gold nanoparticles (AuNPs) may be inspected by the second-harmonic generation (SHG) and two-photon luminescence (TPL) emission from AuNPs. It was revealed that the SHG and TPL signals from AuNPs were sensitive to the substitution of citrate by active hydride species derived from the hydrolysis of NaBH4. Based on the UV-vis spectroscopy analyses and monitoring the SHG/TPL signals, the induction time in the catalytic reaction of 4-nitrothiophenol was revealed to originate from the hindered adsorption of hydride on the gold surface. This work demonstrated that SHG and TPL can provide a new approach for detecting active hydrides on the surface of metallic nanoparticles in colloids.

Ultrafast study of substituted-position-dependent excited-state evolution in benzophenone-carbazole dyads.

Donor and acceptor (D-A) compounds based on benzophenone (BP) and carbazole (Cz) were recently reported to exhibit an extraordinary long afterglow phosphorescence in the solid state. However, the BP derivatives' mechanism of long afterglow phosphorescence is obscure. BP-o-Cz, BP-m-Cz, and BP-p-Cz were designed by coupling Cz at the ortho-, meta- and para-positions of the BP's benzene ring to uncover the excited-state evolution of BP-Cz molecules. Femtosecond and nanosecond transient absorption and excited-state theoretical calculations were carried out to detect and trace the photophysical process of BP-Cz dyads. After the excitation, all dyads experience intramolecular charge transfer (ICT) and intersystem crossing (ISC) processes. The resulting charge-transfer (1CT and 3CT) state of BP-o-Cz will decay to the ground state directly and quickly via the fast charge recombination (CR) process, which may be caused by through-space D-A interaction due to the enforced proximity between BP and Cz. In contrast, for BP-m-Cz and BP-p-Cz dyads, the complete separation of HOMOs and LUMOs leads to extended ICT and slow CR processes, producing an obvious Cz cation radical intermediate and an ultralong-lived triplet state species after the 3CT. Herein, we demonstrated that the excited-state evolution channels could be modified by tuning the substituted positions of D-A dyads. This may pave the way for designing efficient D-A type luminescent materials.

[Features of intestinal flora in children with food protein-induced proctocolitis based on high-throughput sequencing]. / åŸºäºŽé«˜é€šé‡æµ‹åºæŠ€æœ¯åˆ†æžé£Ÿç‰©è›‹ç™½è¯±å¯¼æ€§ç›´è‚ ç»“è‚ ç‚Žæ‚£å„¿è‚ é“èŒç¾¤ç‰¹å¾.

OBJECTIVES: To study the features of intestinal flora in children with food protein-induced proctocolitis (FPIP) by high-throughput sequencing. METHODS: A total of 31 children, aged <6 months, who experienced FPIP after exclusive breastfeeding and attended the outpatient service of the Third Affiliated Hospital of Zunyi Medical University from October 2018 to February 2021 were enrolled as the FPIP group. Thirty-one healthy infants were enrolled as the control group. Fecal samples were collected to extract DNA for PCR amplification. High-throughput sequencing was used to perform a bioinformatics analysis of 16S rDNA V3-V4 fragments in fecal samples. RESULTS: The diversity analysis of intestinal flora showed that compared with the control group, the FPIP group had a lower Shannon index for diversity (P>0.05) and a significantly higher Chao index for abundance (P<0.01). At the phylum level, the intestinal flora in both groups were composed of Firmicutes, Actinobacteria, Proteobacteria, and Bacteroidetes. Compared with the control group, the FPIP group had a significant reduction in the composition ratio of Actinobacteria (P<0.001) and a significant increase in the composition ratio of Proteobacteria (P<0.05). At the genus level, the intestinal flora in the FPIP group were mainly composed of Escherichia, Clostridium, Enterococcus, Klebsiella, and Bifidobacterium, and the intestinal flora in the control group were mainly composed of Bifidobacterium and Streptococcus. Compared with the control group, the FPIP group had a significant reduction in the composition ratio of Bifidobacterium and Ruminococcus (P<0.05) and significant increases in the composition ratios of Clostridium and Shigella (P<0.05). CONCLUSIONS: Compared with the control group, the FPIP group has a reduction in the diversity of intestinal flora and an increase in their abundance, and there are certain differences in several bacterial genera. These results suggest that changes in the composition of intestinal flora at genus level may play an important role in the development and progression of FPIP.

Photocatalytic redox on the surface of colloidal silver nanoparticles revealed by second harmonic generation and two-photon luminescence.

The redox of silver on the surface of Ag nanoparticles (AgNPs) has received extensive attention because of its significant impact on the biological, physical and chemical properties of AgNPs and their applications. Here we demonstrate that the surface redox reaction of AgNPs in colloids may be investigated by the second harmonic generation (SHG) and two-photon luminescence (TPL) emission from the AgNPs. It was revealed that the oxidation of silver on the surface of AgNPs was accelerated upon femtosecond laser excitation, accompanied by a decrease in the SHG and TPL emissions from the AgNPs. The photon-induced reduction of oxidized silver on AgNPs and the formation of surface defects were also revealed by the changes in the SHG and TPL emissions. Size and morphology changes have not been detected by dynamic light scattering and TEM measurements. The changes in the UV-vis extinction spectra were also very weak compared with previous reports. However, the occurrence of redox reactions on the Ag surface upon femtosecond laser irradiation has been confirmed by multiple control experiments. This work demonstrates that SHG and TPL can sensitively probe the subtle structural change on the surface of AgNPs.

Necrostatin-1 Synergizes the Pan Caspase Inhibitor to Attenuate Lung Injury Induced by Ischemia Reperfusion in Rats.

BACKGROUND: Both apoptosis and necroptosis have been recognized to be involved in ischemia reperfusion-induced lung injury. We aimed to compare the efficacies of therapies targeting necroptosis and apoptosis and to determine if there is a synergistic effect between the two therapies in reducing lung ischemia reperfusion injury. METHODS: Forty Sprague-Dawley rats were randomized into 5 groups: sham (SM) group, ischemia reperfusion (IR) group, necrostatin-1+ischemia reperfusion (NI) group, carbobenzoxy-Val-Ala-Asp-fluoromethylketone+ischemia reperfusion (ZI) group, and necrostatin-1+carbobenzoxy-Val-Ala-Asp-fluoromethylketone+ischemia reperfusion (NZ) group. The left lung hilum was exposed without being clamped in rats from the SM group, whereas the rats were subjected to lung ischemia reperfusion by clamping the left lung hilum for 1 hour, followed by reperfusion for 3 hours in the IR group. 1 mg/kg necrostatin-1 (Nec-1: a specific necroptosis inhibitor) and 3 mg/kg carbobenzoxy-Val-Ala-Asp-fluoromethylketone (z-VAD-fmk: a pan caspase inhibitor) were intraperitoneally administrated prior to ischemia in NI and ZI groups, respectively, and the rats received combined administration of Nec-1 and z-VAD-fmk in the NZ group. Upon reperfusion, expressions of receptor-interacting protein 1 (RIP1), receptor-interacting protein 3 (RIP3), and caspase-8 were measured, and the flow cytometry analysis was used to assess the cell death patterns in the lung tissue. Moreover, inflammatory marker levels in the bronchoalveolar lavage fluid and pulmonary edema were evaluated. RESULTS: Both Nec-1 and z-VAD-fmk, either alone or in combination, significantly reduced morphological damage, inflammatory markers, and edema in lung tissues following reperfusion, and cotreatment of z-VAD-fmk with Nec-1 produced the optimal effect. The rats treated with Nec-1 had lower levels of inflammatory markers in the bronchoalveolar lavage fluid than those receiving z-VAD-fmk alone (P < 0.05). Interestingly, the z-VAD-fmk administration upregulated RIP1 and RIP3 expressions in the lung tissue from the ZI group compared to those in the IR group (P < 0.05). Reperfusion significantly increased the percentages of necrotic and apoptotic cells in lung tissue single-cell suspension, which could be decreased by Nec-1 and z-VAD-fmk, respectively (P < 0.05). CONCLUSIONS: Nec-1 synergizes the pan caspase inhibitor to attenuate lung ischemia reperfusion injury in rats. Our data support the potential use of Nec-1 in lung transplantation-related disorders.

Particle adsorption at the oil-water interface studied with second harmonic generation.

In this work, energetics of the adsorption of polystyrene nanoparticles at the hexadecane-water interface was studied with second harmonic generation. The adsorption of positively and negatively charged nanoparticles at the oil-water interface induced a decrease and an increase in the SHG emission from the interface, respectively. This change in the SHG emission, which is similar to that upon the adsorption of ionic surfactants at the hexadecane-water interface, which we reported previously, was then used as an indicator of particle adsorption at the interface. The adsorption free energies of the particles with a diameter of 20 nm at the hexadecane-water interface were found to be -14.7 ± 0.5 kcal mol-1, -14.4 ± 0.4 kcal mol-1 and -15.1 ± 0.3 kcal mol-1 for the amidine, carboxyl and sulfate latex beads, respectively. This result implied that the van der Waals interaction between the oil phase and the polystyrene particles is capable of driving negatively charged particles to the negatively charged hexadecane-water interface. The principle of like dissolves like played a major role in the adsorption of polystyrene particles from the aqueous phase to the oil-water interface. The origin of the SHG emission from the oil-water interface was also discussed.

Surface curvature-dependent adsorption and aggregation of fluorescein isothiocyanate on gold nanoparticles.

The interaction between metallic nanoparticles and fluorescent molecules and its influence on the optical properties of the particles/molecules have been intensively investigated because of their biology and sensing applications. Here, we studied the adsorption and aggregation of a commonly used dye, fluorescein isothiocyanate (FITC), on gold nanoparticles of various diameters. It was observed that the adsorption of FITC on relatively large gold nanoparticles (≥15 nm in diameter) induced quenching in the two-photon fluorescence (TPF) emission from the FITC molecules, while smaller-sized gold nanoparticles (1.6 nm) had no such effect. This difference was interpreted by the fluorescence resonance energy transfer (FRET) between the FITC molecules and the larger gold nanoparticles. At the same time, it was observed that the ratio of TPF quenching was notably higher than the ratio of the FITC molecules chemically adsorbed on the large gold particles. This unexpected observation revealed that the aggregation-induced fluorescence quenching also contributed significantly to the attenuation of the TPF emission. Time-dependent TPF attenuation during the interaction of FITC and the larger gold nanoparticles was recorded and used to confirm this interpretation. With this experimental evidence, a clear picture of the interaction of the FITC molecules on the gold surface was presented: FITC molecules chemically adsorbed on the small gold nanoparticles. However, the relatively larger surface curvature hindered the aggregation of the FITC molecules on the small gold nanoparticles. On the surface of the larger gold nanoparticles, both adsorption and aggregation occured. The influence of the surface curvature on the interfacial structure of the adsorbed molecules on nanoparticles was discussed.

Drastically modulating the structure, fluorescence, and functionality of doxorubicin in lipid membrane by interfacial density control.

In this work, we report on the observation of a drastic modulation of the fluorescence emission of an anticancer drug, doxorubicin, at the lipid interface during the variation of its molecular density at the interface. The emission efficiency of doxorubicin in the lipid membrane was modulated in the range of less than 10% to above 300% that in the aqueous solution. The corresponding changes in the structure and functionality of doxorubicin on the lipid surface were analyzed with the aid of second harmonic generation and theoretical calculation. It was observed that doxorubicin molecules aggregated on the lipid membrane at a relatively high interfacial density. However, this aggregation may not cause interfacial domain large enough to alter the permeability of the lipid bilayer. At an even higher doxorubicin density, the domain of the aggregated doxorubicin molecules induced a cross-membrane transportation.

Cooperative Effects of Zwitterionic-Ionic Surfactant Mixtures on the Interfacial Water Structure Revealed by Sum Frequency Generation Vibrational Spectroscopy.

Cooperative effects of a series of equimolar binary zwitterionic-ionic surfactant mixtures on the interfacial water structure at the air-water interfaces have been studied by sum frequency generation vibrational spectroscopy (SFG-VS). For zwitterionic surfactant palmityl sulfobetaine (SNC16), anionic surfactant sodium hexadecyl sulfate (SHS), and cationic surfactant cetyltrimethylammonium bromide (CTAB) with the same length of alkyl chain, significantly enhanced ordering of interfacial water molecules was observed for the zwitterionic-anionic surfactant mixtures SNC16-SHS, indicating that SNC16 interacts more strongly with SHS than with CTAB because of the strong headgroup-headgroup electrostatic attraction for SNC16-SHS. Meanwhile, the SFG amplitude ratio of methyl and methylene symmetric stretching modes was used to verify the stronger interaction between SNC16 and SHS. The conformational order indicator increased from 0.64 for SNC16 to 7.17 for SNC16-SHS but only 0.94 for SNC16-CTAB. In addition, another anionic surfactant sodium dodecyl sulfate (SDS) was introduced to study the influence of chain-chain interaction. Decreased SFG amplitude of interfacial water molecules for SNC16-SDS was observed. Therefore, both the headgroup-headgroup electrostatic interaction and chain-chain van der Waals attractive interaction of the surfactants play an important role in enhancing the ordering of interfacial water molecules. The results provided experimental and theoretical bases for practical applications of the surfactants.

Lyophobicity may not be the main driving force for long chain surfactants from the bulk phase to the interface.

According to the Traube rule, a surfactant with a longer alkane chain is more hydrophobic so its tendency to be driven from a polar solvent to a less polar interface is higher. In this work, we revisited this topic by studying the adsorption of quaternary ammonium salts and carboxylic acids with various alkane chain lengths at the hexadecane-water interface. The adsorption free energies of the surfactants at this oil-water interface from the polar (aqueous solution) or nonpolar phase (hexadecane) were estimated from second harmonic generation measurements. The variation of the free energies per methylene group in the bulk phase, at the oil-water interface and at the air-water interface revealed that there are different interactions between the alkane chains of the surfactants in different environments. The chain-chain interaction at the hexadecane-water interface is lower than that at the air-water interface. The driving force for the alkane chains to adsorb at the oil-water interface from the oil phase is close to that from the aqueous phase. This observation reveals that the chain-chain interaction rather than the lyophobicity of the solute with respect to the solvent is the main contributor to the adsorption free energy. This is the first experimental comparison of the free energies of the alkane chains in oil, in water, at the air-water interface and at the oil-water interface. These results provide information for studying the interactions of hydrophobic species in different environments. This work also provides a method for estimating the solvation energy of some head groups in surfactants.

The ionic strength dependent zeta potential at the surface of hexadecane droplets in water and the corresponding interfacial adsorption of surfactants.

An anomalous maximum in the ionic strength dependent electrophoretic mobility curves has been observed in previous reports from particles dispersed in colloids. This maximum has been considered anomalous because it is contradictory with the Gouy-Chapman model. The existence of such a maximum has been attributed to specific ionic adsorption, a hairy layer at the surface, or the effect of the anomalous change of surface conductivity in different studies. It was also pointed out that the O'Brien-White approach based on the Gouy-Chapman model could be used to understand this maximum in electrophoretic mobility curves and lead to understandable zeta potential curves. This implied that the observed maximum was actually not "anomalous". In this work we report our simulation of ionic strength dependent zeta potential curves based on the O'Brien-White approach and experimental studies of the ionic strength dependent electrophoretic mobility of the hexadecane droplets in the hexadecane-water emulsions at different pH or in the presence of sodium dodecyl sulphate at varied concentrations. In some cases, the simulation shows that the calculation with the O'Brien-White approach does change the trend in the concerned ionic strength dependent curves. However, the simulation in some other cases also leads to similar trends in the ionic strength dependent electrophoretic mobility curves and zeta potential curves. In the experiments, both the existence and non-existence of such a maximum were observed and demonstrated to be system dependent. The corresponding molecular structure of the oil-water interface was then discussed with the analyses of the zeta potential curves and second harmonic generation signals recorded at the hexadecane-water interface.

Homogeneous and inhomogeneous broadenings and the Voigt line shapes in the phase-resolved and intensity sum-frequency generation vibrational spectroscopy.

In this report, we show that the ability to measure the sub-1 cm(-1) resolution phase-resolved and intensity high-resolution broadband sum frequency generation vibrational spectra of the -CN stretch vibration of the Langmuir-Blodgett (LB) monolayer of the 4-n-octyl-4'-cyanobiphenyl (8CB) on the z-cut α-quartz surface allows the direct comparison and understanding of the homogeneous and inhomogeneous broadenings in the imaginary and intensity SFG vibrational spectral line shapes in detail. The difference of the full width at half maximum (FWHM) of the imaginary and intensity sum-frequency generation vibrational spectroscopy spectra of the same vibrational mode is the signature of the Voigt line shape and it measures the relative contribution to the overall line shape from the homogeneous and inhomogeneous broadenings in SFG vibrational spectra. From the phase-resolved and intensity spectra, we found that the FWHM of the 2238.00 ± 0.02 cm(-1) peak in the phase-resolved imaginary and intensity spectra is 19.2 ± 0.2 cm(-1) and 21.6 ± 0.4 cm(-1), respectively, for the -CN group of the 8CB LB monolayer on the z-cut α-quartz crystal surface. The FWHM width difference of 2.4 cm(-1) agrees quantitatively with a Voigt line shape with a homogeneous broadening half width of Γ = 5.29 ± 0.08 cm(-1) and an inhomogeneous standard derivation width Δω = 5.42 ± 0.07 cm(-1). These results shed new lights on the understanding and interpretation of the line shapes of both the phase-resolved and the intensity SFG vibrational spectra, as well as other incoherent and coherent spectroscopic techniques in general.

Molecular interactions at the hexadecane/water interface in the presence of surfactants studied with second harmonic generation.

It is important to investigate the influence of surfactants on structures and physical/chemical properties of oil/water interfaces. This work reports a second harmonic generation study of the adsorption of malachite green (MG) on the surfaces of oil droplets in a hexadecane/water emulsion in the presence of surfactants including sodium dodecyl sulfate, polyoxyethylene-sorbitan monooleate (Tween80), and cetyltrimethyl ammonium bromide. It is revealed that surfactants with micromolar concentrations notably influence the adsorption of MG at the oil/water interface. Both competition adsorption and charge-charge interactions played very important roles in affecting the adsorption free energy and the surface density of MG at the oil/water interface. The sensitive detection of the changing oil/water interface with the adsorption of surfactants at such low concentrations provides more information for understanding the behavior of these surfactants at the oil/water interface.

Influence of different types of Phyllostachys pubescens (Poales: Poaceae) leaves on population parameters of Pantana phyllostachysae (Lepidoptera: Lymantriidae) and parasitic effects of Beauveria bassiana (Moniliales: Moniliaceae).

We found that Pantana phyllostachysae, a dangerous pest of moso bamboo (Phyllostachys pubescens), showed differences in growth and development after feeding on diverse types of moso bamboo leaves. The mortality rate of Pa. phyllostachysae due to Beauveria bassiana, an entomopathogenic fungus, was also affected by the varied larval diet. Larval and pupal developmental duration of Pa. phyllostachysae was longer when feeding on "off-year" bamboo leaves. Pupal weight and adult fertility were higher when feeding on "on-year" bamboo leaves. Mortality due to B. bassiana was significantly lower in larvae fed on on-year bamboo leaves than in larvae fed on off-year bamboo leaves. Larvae fed on new bamboo leaves had a shorter development period and higher survival rate than those fed on off-year bamboo leaves. However, mixed feed (mixture of new, on-year, and off-year bamboo leaves) decreased the egg production of Pa. phyllostachysae. After infection by the second generation of B. bassiana, the survival time of Pa. phyllostachysae fed on mixed feed increased significantly compared with the first generation. We also fed Pa. phyllostachysae different proportion of new bamboo leaves in mixed feed to simulate natural conditions. We found that increasing the proportion of new bamboo leaves in the food promoted pupal development and increased egg production; it also increased the resistance of larvae to the first generation of B. bassiana. The pathogenicity of the second generation of B. bassiana declined in all mixed feed treatments.