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Climate change has been driving long-distance migratory birds to alter their schedules under the threat of being mismatched with their food peak at the breeding grounds. It is important to study the relative contribution of environmental, genetic and ontogenetic components in various spring timing traits in the wild in order to predict the true potential for migratory birds to adapt to the changing environment. We aimed to detect if heritable and ontogenetic components can explain variation in the timing of spring migration and breeding in pied flycatchers (Ficedula hypoleuca). Geolocator tracks of 44 locally hatched birds deployed during 2016-2019 in the Netherlands and the United Kingdom were used to investigate the role of early-life traits in the pre-fledging phase, as well as parental timings, in contributing to individual differences in the timing of spring migration and breeding in adulthood. We found a positive relationship between an individuals’ birth date and spring departure date from Africa in adulthood, but not for breeding arrival or laying date. Variation in spring departure date could not be explained by any other early-life trait in the pre-fledging phase, yet was well explained by the arrival dates of its parents in its birth year. This suggests that under natural conditions, individual differences in spring departure timing have a strong heritable component (in the broad sense), but that environmental conditions experienced along the migratory route and at breeding sites are partially masking this expression in arrival and laying schedules in these early breeding populations. Such environmental masking may reduce heritability in the timing of arrival and laying, thereby slowing down climatic adaptation towards earlier time schedules in pied flycatchers.

Evidence accumulates that dispersal is correlated with individual behavioural phenotype (dispersal syndrome). The evolutionary causes and consequences of such covariation depend on the degree of plasticity versus inheritance of the traits, which requires challenging experiments to implement in mobile organisms. Here, we combine a forced dispersal experiment, natural colonization and longitudinal data to establish if dispersal and aggression levels are integrated and to test their adaptive nature in pied flycatchers ( Ficedula hypoleuca ). We found that (forced) dispersers behaved more aggressively in their first breeding year after dispersal and decreased their aggression in following years. Strength of dispersal syndrome and direction of fecundity selection on aggression in newly colonized areas varied between years. We propose that the net benefits of aggression for dispersers increase under harsh conditions (e.g. low food abundance). This hypothesis now warrants further testing. Overall, this study provides unprecedented experimental evidence that dispersal syndromes can be remodelled via adaptive plasticity depending on the individuals' local breeding experience and/or year-specific ecological conditions. It highlights the importance of individual behavioural variation in population dynamics.

Study Objectives To investigate trajectories of early childhood sleep in the first 3 years and their association with maternal depressive symptoms. Methods Data were from 243 Chinese mother–child dyads. Children’s sleep duration and night-waking were assessed using the Brief Infant Sleep Questionnaire (BISQ) at 42 days, 3, 6, 9, 12, 18, 24, and 36 months postpartum. The Center for Epidemiological Survey-Depression Scale (CES-D), Edinburgh Postnatal Depression Scale (EPDS), and Profile of Mood States (POMS) were used to assess maternal depressive symptoms at late pregnancy, 42 days, and 36 months postpartum, respectively. Early childhood sleep trajectories were estimated with group-based trajectory models. The association between early childhood sleep trajectories and maternal depressive symptoms was examined with binary and multinomial logistic regression models and linear regression models. Results Three trajectories of daytime sleep duration (“short”, 14.4%; “medium”, 60.4%; “long”, 25.2%), nighttime sleep duration (“increasing”, 17.6%; “stable”, 76.3%; “decreasing”, 6.1%), and total sleep duration (“short”, 21.5%; “medium”, 59.9%; “long”,18.6%), and two trajectories of night-waking (“resolving”, 22.9%; “persistent”, 77.1%) were identified. Controlling for confounding factors, maternal depression at 42 days postpartum was associated with higher risks for short daytime sleep duration and persistent night-waking in children. Persistent night-waking in children was associated with increased maternal depressive symptoms at 36 months postpartum. Conclusion Early childhood sleep follows distinct trajectories in the first 3 years of life. The trajectories of short daytime sleep duration and persistent night-waking are associated with maternal depression. The findings indicate tailored interventions should target both unfavorable early childhood sleep trajectories and maternal depression.

Background: Overweight/obesity may impair executive function (EF). However, adolescent EF impairments across the weight spectrum were not well studied, with the moderating effect of negative emotions in the weight-EF association being limitedly investigated. We aimed to determine whether overall and abdominal weight spectrum associated with EF impairments and to identity whether negative emotions moderate the weight-EF link in adolescents. Methods: We applied a subsample of the SCHEDULE-A project. Adolescents (11-18 years) were recruited using a multi-stage cluster random sampling approach. Overall and abdominal weight were measured by body mass index z-score and waist-to-height ratio, respectively. We used the Behavior Rating Inventory of Executive Function (BRIEF) to evaluate adolescent EF in nature setting, and utilized the Depression Anxiety and Stress Scales (DASS-21) to assess three types of negative emotional states (i.e., depression, anxiety, and stress). Results: Of the 1 935 adolescents, 963 (49.8%) were male. We observed that abdominal, not overall, overweight was associated with the Global Executive Composite (GEC) impairment (OR = 1.59, 95% CI: 1.07-2.35), particularly for inhibit, emotion control, shift, working memory, and monitor domains. Furthermore, depression moderated the abdominal overweight-GEC association (P = 0.032 for interaction term), especially for emotional control, working memory, and initiate dimensions. Moreover, we also found abdominal thinness was associated with the Metacognition Index problem (OR = 1.33, 95% CI: 1.04-1.72), particularly for plan and monitor areas. Conclusions: Both abdominal overweight and thinness were associated with adolescent EF, and depression would be a modifiable target to improve EF in adolescents with abdominal overweight.

Pinus koraiensis, Pinus sibirica, and Pinus pumila are the major five-needle pines in northeast China, with substantial economic and ecological values. The phenotypic variation, environmental adaptability and evolutionary relationships of these three five-needle pines remain largely undecided. It is therefore important to study their genetic differentiation and evolutionary history. To obtain more genetic information, the needle transcriptomes of the three five-needle pines were sequenced and assembled. To explore the relationship of sequence information and adaptation to a high mountain environment, data on needle morphological traits [needle length (NL), needle width (NW), needle thickness (NT), and fascicle width (FW)] and 19 climatic variables describing the patterns and intensity of temperature and precipitation at six natural populations were recorded. Geographic coordinates of altitude, latitude, and longitude were also obtained. The needle morphological data was combined with transcriptome information, location, and climate data, for a comparative analysis of the three five-needle pines. We found significant differences for needle traits among the populations of the three five-needle pine species. Transcriptome analysis showed that the phenotypic variation and environmental adaptation of the needles of P. koraiensis, P. sibirica, and P. pumila were related to photosynthesis, respiration, and metabolites. Analysis of orthologs from 11 Pinus species indicated a closer genetic relationship between P. koraiensis and P. sibirica compared to P. pumila. Our study lays a foundation for genetic improvement of these five-needle pines and provides insights into the adaptation and evolution of Pinus species.

Miscarriage is the most common adverse pregnancy outcome and more than 50% of its incidence remains unexplained. Earlier studies have suggested that maternal microbiota might be associated with miscarriage, but the association is insufficiently understood.We used 16S ribosomal RNA (rRNA) amplicon sequencing and metagenomic sequencing technology to characterize the bacterial composition of three sites including the rectum, vagina, and cervix of a case group of 63 pregnant women who had miscarried compared to a control group of 24 pregnant women who underwent voluntary elective abortion.The alpha-diversity from the rectum and cervix was significantly decreased in the case group relative to the control group. However, we did not find significant differences in microbial diversity of vaginal samples between the two groups.We detected a significantly lower rectal microbiota diversity and a pro-inflammatory tendency in the miscarriage group. This is the first study to investigate the association of microbiota from samples collected from three sites and miscarriage. Further studies are warranted to explore further the role of microbiota in miscarriage.

In order to solve the problem of freezing damage treatment and anti-freezing design for railway tunnels in operation in the seasonal frozen area, this paper proposes a polyurethane-corrugated steel plate insulation lining, and studies its thermal insulation effect, relying on a freezing damage treatment project of an existing passenger-dedicated tunnel for on-site application. In this paper, the insulation lining is applied to the actual project and the insulation effect is verified by the field monitoring. The temperature test section was set in the anti-freezing design section. The polyurethane-corrugated steel plate insulation lining proposed in this paper is mainly composed of corrugated steel plate, polyurethane insulation layer and waterproof layer. The polyurethane-corrugated steel insulation lining is applied by using self-made rail flat battery car, door-type scaffolding, arch slide and other construction equipments. The on-site temperature test shows that the insulation effect is obvious. The polyurethane-corrugated steel plate insulation lining has the advantages of fast construction speed, good thermal insulation effect, preventing concrete from peeling off blocks, easy removal and replacement. According to the field temperature test, under the natural temperature outside the tunnel from −18°C to −22°C in winter of 2018–2020, the temperature of the interface between surrounding rock and lining of the tunnel monitoring sections are all above 0°C so that the freezing damage is eliminated from the root. Research results can provide a theoretical basis for the anti-freezing projects of tunnels in seasonal frozen area.

Introduction Autism spectrum disorder (ASD) is a complex and prevalent neurodevelopmental disorder characterized by deficits in social communication and social interaction as well as repetitive behaviors. Alterations in function connectivity are widely recognized in recent electroencephalogram (EEG) studies. However, most studies have not reached consistent conclusions, which could be due to the developmental nature and the heterogeneity of ASD. Methods Here, EEG coherence analysis was used in a cohort of children with ASD (n = 13) and matched typically developing controls (TD, n = 15) to examine the functional connectivity characteristics in long‐distance and short‐distance electrode pairs. Subsequently, we explore the association between the connectivity strength of coherence and symptom severity in children with ASD. Results Compared with TD group, individuals with ASD showed increased coherence in short‐distance electrode pairs in the right temporal–parietal region (delta, alpha, beta bands), left temporal–parietal region (all frequency bands), occipital region (theta, alpha, beta bands), right central–parietal region (delta, alpha, beta bands), and the prefrontal region (only beta band). In the long‐distance coherence analysis, the ASD group showed increased coherence in bilateral frontal region, temporal region, parietal region, and frontal–occipital region in alpha and beta bands. The strength of such connections was associated with symptom severity. Discussion Our study indicates that abnormal connectivity patterns in neuroelectrophysiology may be of critical importance to acknowledge the underlying brain mechanism., Alterations in function connectivity are widely recognized in recent electroencephalogram (EEG) studies. Our study indicates that discovery of atypical brain coherence in ASD young children may be of a critical importance to acknowledge the underlying brain mechanism.

Backgroud Autism spectrum disorders (ASD) are a complex group of neurodevelopmental disorders with a genetic basis. The role of long-chain polyunsaturated fatty acids (LC-PUFAs) and the occurrence of autism has been the focus of many recent studies. The present study investigates whether genetic variants of the fatty acid desaturase (FADS) 1/2 and elongation of very long-chain fatty acids protein (ELOVL) 2 genes, which are involved in LC-PUFA metabolism, are associated with ASD risk. Methods A cohort of 243 ASD patients and 243 unrelated healthy controls were enrolled in this case control study. Sixteen tag single nucleotide polymorphisms from the FADS1–2 and ELOVL2 genes were genotyped using the Sequenom Mass Array. Results There were significant differences in allelic distribution of FADS2 rs526126 (OR = 0.55, 95% CI = 0.42–0.72, pFDR

Autism spectrum disorder (ASD) is a neurodevelopment disorder with abnormalities of social interaction, communication and repetitive behaviors. The higher prevalence of ASD in men implies a potential relationship between sex hormones and ASD etiology. The ESR2 gene encodes estrogen receptor beta (ESR2) and plays an important role during brain development. A relationship between ESR2 and ASD has been suggested by studies on single nucleotide polymorphisms and mRNA and protein expression levels in ASD patients. Here, we explored the possible epigenetic regulation of the ESR2 gene in autism. We collected genomic DNA from the peripheral blood of Chinese Han males with autism and age-matched normal males and measured DNA methylation of CpG islands in the ESR2 gene, which consisted of 41 CpG sites among the proximal promoter region and an untranslated exon, by bisulfite sequencing. We also investigated a relationship between DNA methylation and phenotypic features of autism, as assessed by the Children Autism Rating Scale. We found little overall difference in the DNA methylation of the ESR2 5'-flanking region in individuals with autism compared with normal individuals. However, detailed analyses revealed that eight specific CpG sites were hypermethylated in autistic individuals and that four specific CpG sites were positively associated with the severity of autistic symptoms. Our study indicates that the epigenetic dysregulation of ESR2 may govern the development of autism.

We examined and analyzed binocular imbalance in a group of randomly selected normal subjects with corrected visual acuity of 0.8 or more in both eyes without ocular diseases, by using augmented virtual reality system. This study will quantify the correlation between binocular imbalance in these normal subjects and various spatial frequencies and temporal frequencies in the integrated binocular stimulation mode. A retrospective study was carried out and data from 97 patients (51 males and 46 females) who were diagnosed with no eye diseases, and with corrected binocular visual acuity of 0.8 or more, were collected. Their binocular visual function, Hirschberg test refraction status, and binocular imbalance were assessed using the quantified visual perception stimulation mode in an augmented virtual reality platform. When normal subjects (with corrected binocular vision of 0.8 or more without ocular diseases) were assessed using the integrated binocular stimulation mode with different temporal and spatial frequencies, a gradual reduction of binocular imbalance could be observed when spatial frequencies were increased. When contrast balance was adjusted, binocular imbalance was more prevalent in the horizontal state compared with the vertical state. This was seen when patients were stimulated by different temporal frequencies in the virtual reality testing mode. 17.53% and 29.90% of participants reached complete binocular fusion under low temporal frequency stimulation and high temporal frequency stimulation, respectively, while binocular imbalance was found in 65.9% and 62.89% of participants who were stimulated, respectively, by low temporal frequency and high temporal frequency. In addition, 16.5% and 7.21% experienced severe binocular imbalance under low temporal and high temporal frequency stimulation, respectively. The integrated binocular stimulation mode under low temporal frequency was more sensitive in detecting binocular imbalance. The status of binocular balance in normal subjects was not the same when stimulated by the augmented virtual reality platform, as many showed varying degrees of binocular imbalance. The results from our clinical study demonstrate that integrated binocular stimulation with different spatial and temporal frequencies enables a more sensitive detection of binocular imbalance, making it a powerful new tool for the diagnosis and analysis of clinical binocular abnormalities. In addition, since more than half of the normal subjects (without eye diseases who has corrected vision of 0.8 or more) exhibited binocular imbalance in our study, we believe that this brief binocular imbalance is likely a transient physiological phenomenon, which is not pathological to visual acuity and function, and should only be seen as pathological when binocular imbalance is prolonged, causing functional deficits such as reading impairment.

Rationale: This study aimed to investigate the genetic mutation characteristics of congenital idiopathic hypogonadotropic hypogonadism (IHH) through the clinical features and genetic analysis of 2 patients with IHH in 1 pedigree. Patient concerns: A 23-year-old girl presented with primary amenorrhea, sparse pubic hair, lack of breast development, and delayed sexual development. Diagnoses: Combined with the clinical characteristics, auxiliary examinations, and molecular genetic analysis, the patient was diagnosed as IHH. Interventions: Whole exome and Sanger sequencing were performed to validate the mutation in family members. Outcomes: A novel homozygous missense mutation c.521A > G (p.Q174R) in the GNRHR gene was identified in the 2 affected sisters. Familial segregation showed that the homozygous variant was inherited from their parents respectively and the eldest sister was the carrier without correlative symptom. Lessons: We reported a novel GNRHR mutation in a pedigree with congenital idiopathic hypogonadotropic hypogonadism. Glutamine at amino acid position 174 was highly conserved among various species. The molecular structure of GNRHR protein showed that p.Q174R mutation brought in a new stable hydrogen bond between position 174 and 215, may impede conformational mobility of the TMD4 and TMD5. It suggests that the missense mutation c.521A > G related to congenital idiopathic hypogonadotropic hypogonadism was probably a causative factor for both sisters. Through high-throughput sequencing and experimental verification, we had basically determined the patient's pathogenic mutation and inheritance, which could better guide doctors for treatment.

Prenatal exposure to valproic acid (VPA) in rat offspring is capable of inducing experimental autism with neurobehavioral aberrations. This study investigated the effect of docosahexaenoic acid (DHA) on hippocampal cell death, learning and memory alteration in an experimental rat autism model. We found that DHA supplementation (75, 150 or 300 mg/kg/day, 21 days) rescued the VPA (600 mg/kg) induced DHA reduction in plasma and hippocampus in a dose-dependent manner, increased the levels of hippocampal p-CaMKII and p-CREB without affecting total protein level, and altered BDNF-AKT-Bcl-2 signaling pathway, as well as inhibited the activity of caspase-3. DHA also influenced the content of malondialdehyde (MDA) and the activities of antioxidant enzymes in the VPA-treated offspring. Consistent with the previous results, we also observed that 300 mg/kg DHA supplementation markedly increased the cell survival, decreased the cell apoptosis, and increased mature neuronal cell in the hippocampus in VPA-treated offspring. Utilizing the Morris water maze test, we found that DHA prevented cognitive impairment in offspring of VPA-treated rats. The data suggested that DHA may play a neuroprotective role in hippocampal neuronal cell and ameliorates dysfunctions in learning and memory in this rat autism model. Thus, DHA could be used as treatment intervention for mitigating behavioral dysfunctions in autism spectrum disorder (ASD).

Objective: A study in a Caucasian population has identified two single-nucleotide polymorphisms (SNPs) in ZNF533, one in DOCK4, and two in IMMP2L, which were all significantly associated with autism. They are located in AUTS1 and AUTS5, which have been identified as autism susceptibility loci in several genome-wide screens. The present study aimed to investigate whether ZNF533, DOCK4, and IMMP2L genes are also associated with autism in a northeastern Chinese Han population. Methods: We performed a similar association study using families with three individuals (one autistic child and two unaffected parents). A family-based transmission disequilibrium test (TDT) was used to analyze the results. Results: There were significant associations between autism and the two SNPs of ZNF533 gene (rs11885327: χ 2=4.5200, P=0.0335; rs1964081: χ 2=4.2610, P=0.0390) and the SNP of DOCK4 gene (rs2217262: χ 2=5.3430, P=0.0208). Conclusions: Our data suggest that ZNF533 and DOCK4 genes are linked to a predisposition to autism in the northeastern Chinese Han population.

CdS quantum dots(QDs) sensitized TiO2 nanotube arrays photoelectrodes were investigated for their photovoltaic performance of quantum dots-sensitized solar cells. The highly ordered TiO2 nanotube arrays(TNAs) were synthesized on Ti foils by anodic oxidation method. Then CdS quantum dots were deposited onto the TiO2 nanotube arrays by successive ionic layer absorption and reaction(SILAR) method to serve as the sensitizers. Cd(NO3)2 and Na2S were used as the precursor materials of Cd+ and S2− ions, respectively. It is found that the CdS QDs sensitizer may significantly increase the light response of TiO2 nanotube arrays. With increasing CdS QDs deposition cycles, the visible light response increases. Maximum photocurrent was obtained for the QDs that have an absorption peak at about 500 nm. Under AM 1.5 G illuminations(100 mW cm−2), a 4.85 mA/cm2 short circuit current density was achieved, and the maximium energy conversion efficiency of the asprepared CdS QDs-sensitized TNAs solar cells was obtained as high as 0.81 % at five SILAR cycles.

CdS quantum dots (QDs)-sensitized TiO2 film with three-dimensionally (3D) ordered macropores was synthesized via a two-step method on ITO glass substrate. 3D-ordered macroporous TiO2 film was firstly fabricated on an ITO glass via layer-by-layer deposition and hydrolysis of tetrabutyl titanate using 3D-ordered latex film as organic template, followed by calcination at 450 degrees C for 2 h to remove the template. Then, the CdS QDs were deposited on the 3D-ordered macroporous TiO2 film by successive ionic layer adsorption and reaction technique. The as-prepared CdS-sensitized TiO2 film was characterized with X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, transmission electron microscopy, diffusive reflectance UV-visible absorption spectra, and photoelectrochemical measurements. Its photocatalytic activity was evaluated by the photocatalytic degradation of crystal violet aqueous solution at ambient temperature. It was revealed in our results that the CdS QDs-sensitized 3D-ordered macroporous TiO2 film exhibits enhanced photocatalytic activity for the photodegradation of crystal violet than that of the CdS-free 3D-ordered macroporous TiO2 film and that of CdS QD-sensitized TiO2 film without 3D-ordered macropores under the irradiation of visible light due to the co-existence of 3D-ordered interconnected macropores and the sensitization of CdS QDs.

Aims To investigate the effect of FTY720 on the valproic acid (VPA) rat model of autism. Main methods As an animal model of autism, we used intraperitoneal injection of VPA on embryonic day 12.5 in Wistar rats. The pups were given FTY720 orally at doses of 0.25, 0.5 and 1 mg/kg daily from postnatal day 15 to 35. Social behavior, spatial learning and memory were assessed at the end of FTY720 treatment. The histological change, oxidative stress, neuroinflammatory responses, and apoptosis-related proteins in the hippocampus were evaluated. Key findings FTY720 (1 mg/kg) administration to VPA-exposed rats (1) improved social behavior, spatial learning and memory impairment; (2) resulted in a reduction in neuronal loss and apoptosis of pyramidal cells in hippocampal CA1 regions; (3) inhibited activation of microglial cells, in turn lowering the level of pro-inflammatory cytokines interleukin-1β (IL-1β) and IL-6 in the hippocampus; (4) changed Malondialdehyde (MDA) levels, Glutathione (GSH) levels, superoxide dismutase (SOD) activity and Glutathione Peroxidase (GSH-Px) activity in the hippocampus; (6) inhibited the elevated Bax and caspase-3 protein levels and enhanced the relative expression level of Bcl-2 in the hippocampus; and (7) increased phospho-Ca2 +/calmodulin-dependent protein kinase II (p-CaMKII), phospho-cAMP-response element binding protein (p-CREB) and Brain Derived Neurotrophic Factor (BDNF) protein expression in the hippocampus. Significance FTY720 rescues social deficit, spatial learning and memory impairment in VPA-exposed rats. FTY720 exerts both a direct protection for neurons and an indirect modulation of inflammation-mediated neuron loss as a possible mechanism of neuroprotection.

A double-layer TiO2 nanotube arrays were formed by two-step anodization of Ti foils in different electrolytes. First, Ti in 0.5 wt% HF was anodized to form thin nanotube layer. Afterwards a second anodization was conducted in a formamide based electrolyte, which allowed the second layer of nanotube growing directly underneath the first one. From FESEM investigation we found that the thickness of second layer corresponded to the anodization time, the increasing of which would lead to the excessive etching on the first layer. The first layer protected the lower one from fluoride corrosion during anodization process. The double layer TiO2 nanotube arrays showed no benefit to photodegradation effect in methyl orange degradation experiments.

Nitrogen-doped titanium dioxide mesosponge was fabricated by transformation of TiO2 nanotube arrays using a facial solvothermal method. The structure, morphology and optical property were investigated by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and UV–vis diffusion reflection spectroscopy (DRS). A possible formation mechanism of N-doped TiO2 mesosponge has been proposed. The photoelectrochemical results indicate that N-doped TiO2 mesosponge prepared in ethanol solution of ammonia exhibits much higher photocurrent densities and the optimal photocatalytic activity.

To investigate whether the decreased level of serum polyunsaturated fatty acids (PUFAs) in patients with autism is associated with the expression of related liver metabolic enzymes, we selected rats that were exposed to valproic acid (VPA) on embryonic day 12.5 (E12.5) as a model of autism. We observed the serum levels of PUFAs and the expression of related liver metabolic enzymes, including Δ5-desaturase, Δ6-desaturase and elongase (Elovl2), in VPA-exposed and control rats on postnatal day 35 (PND35) and conducted sex dimorphic analysis. We found that the levels of serum PUFAs and related liver metabolic enzymes in the VPA rats were significantly reduced, in association with autism-like behavioral changes, the abnormal expression of apoptosis-related proteins and hippocampal neuronal injury, compared to the control rats and showed sex difference in VPA group. This finding indicated that rats exposed to VPA at the embryonic stage may exhibit reduced synthesis of serum PUFAs due to the down-regulation of liver metabolic enzymes, thereby inducing nervous system injury and behavioral changes, which is affected by sex in the meantime.

Raman investigations were carried out for various compositions of chalcogenide glasses in the GeS2–Ga2S3–CdS system. Addition of Ga2S3 into GeS2 results in the formation of metal–metal bonds and edge-shared GaS4/2 tetrahedra. Ge2+ ions may surround [GaS4/2]1− tetrahedra acting as charge compensators. Upon the addition of CdS into the GeS2–Ga2S3 system, the number of the metal–metal bonds and edge-shared GaS4/2 tetrahedra decreases, resulting in the formation of corner-shared tetrahedra with non-bridging sulfurs (NBS). Cd2+ ions can be dissolved into the glass network as charge compensators for these NBS and exited few [GaS4/2]1− tetrahedra. The high solubility of CdS is ascribed to the dissociation of metal–metal bonds and edge-shared tetrahedra in these Ga-containing glasses.

Front-side illuminated solar cells with CdS quantum dots (QDs) incorporated with free-standing through-hole TiO2 nanotube arrays (TNAs) were developed. The solar cells, based on TNAs with different lengths that were sensitized by successive ionic layer adsorption and reaction method (SILAR) with various cycles, have been tested. The morphology and crystalline phase of the TiO2 nanotubes were studied by field emission scanning electron microscopy (FESEM) and X-ray diffraction (XRD). The crystallized free-standing through-hole TNAs were easily transferred to the fluorine-doped tin oxide glass to form a photoanode by slightly modifying the anodization procedure. The SILAR technique enables us to control the loading amount and particle size of CdS QDs by altering deposition cycles. The cells with TNAs ca. 20 μm long (obtained by anodization for 4 h) and 5 SILAR cycles show a photovoltaic conversion efficiency as high as 1.187% under simulated sunlight (AM 1.5, 100 mW cm(-2)).

CdS quantum dots (QDs)-sensitized TiO2 film with three-dimensionally (3D) ordered macropores was synthesized via a two-step method on ITO glass substrate. 3D-ordered macroporous TiO2 film was firstly fabricated on an ITO glass via layer-by-layer deposition and hydrolysis of tetrabutyl titanate using 3D-ordered latex film as organic template, followed by calcination at 450 degrees C for 2 h to remove the template. Then, the CdS QDs were deposited on the 3D-ordered macroporous TiO2 film by successive ionic layer adsorption and reaction technique. The as-prepared CdS-sensitized TiO2 film was characterized with X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, transmission electron microscopy, diffusive reflectance UV-visible absorption spectra, and photoelectrochemical measurements. Its photocatalytic activity was evaluated by the photocatalytic degradation of crystal violet aqueous solution at ambient temperature. It was revealed in our results that the CdS QDs-sensitized 3D-ordered macroporous TiO2 film exhibits enhanced photocatalytic activity for the photodegradation of crystal violet than that of the CdS-free 3D-ordered macroporous TiO2 film and that of CdS QD-sensitized TiO2 film without 3D-ordered macropores under the irradiation of visible light due to the co-existence of 3D-ordered interconnected macropores and the sensitization of CdS QDs.

V-doped TiO(2)nanoparticles were synthesized at low temperature and characterized by X-ray diffraction (XRD), Raman spectroscopy (RS), transmission electron microscopy (TEM), Brunauer-Emmet-Teller (BET), X-ray photoelectron spectroscopy (XPS), UV-vis spectroscopy, and photoluminescence (PL) spectroscopy, respectively. It is found the nanoparticle shape changed from needle, to short stick and then to cubic with the increase of doped V concentration, which was also accompanied by the improvement of crystallinity. The specific surface area (S(BET)) decreased with increasing V content. It is confirmed that V ions can be doped in TiO(2) by substituting Ti(4+) ions, which suppressed the CB --> VB and surface recombination of photoinduced electrons and holes, and a relation was found between the PL spectra and the UV photocatalytic activity. There was an optimum V content for the V-doped TiO(2) to present the best UV-light induced photoactivity, but they were visible-inactive. At last, the effect of the doping V as trapping centers on photocatalysis was investigated in detail, and used to explain the difference between the photocatalysis under the illumination of UV light and visible light.

Carbon-doped TiO2 nanotube arrays (TNAs) were prepared from carbonaceous Ti foils by anodisation in a mixed electrolyte of glycerol and water. The photocatalytic ability can be increased by applying an external positive bias. Enhancing acidity of the pending solution can further accelerate the degradation rate. However, falcate and annular scraps were observed on the surface of TNAs after photoelectrodegradation experiments. XPS analysis indicated that carbon ions were positioned in interstitial site of the catalyst and the carbon content in TNAs decreased following the degradation process. The acid environment can increase the photocatalytic activity; this will damage the C-TNAs greatly. The carbon content decrease from 18.47 at. % to approximate 6 at. % after PEC processes, indicating that the carbon elements is removed from carbonaceous C-TNAs during PEC.

Background Autism is a common, severe and highly heritable neurodevelopmental disorder in children, affecting up to 100 children per 10,000. The MET gene has been regarded as a promising candidate gene for this disorder because it is located within a replicated linkage interval, is involved in pathways affecting the development of the cerebral cortex and cerebellum in ways relevant to autism patients, and has shown significant association signals in previous studies. Principal Findings Here, we present new ASD patient and control samples from Heilongjiang, China and use them in a case-control and family-based replication study of two MET variants. One SNP, rs38845, was successfully replicated in a case-control association study, but failed to replicate in a family-based study, possibly due to small sample size. The other SNP, rs1858830, failed to replicate in both case-control and family-based studies. Conclusions This is the first attempt to replicate associations in Chinese autism samples, and our result provides evidence that MET variants may be relevant to autism susceptibility in the Chinese Han population.