The Impact of Interactive Shared Book Reading on Children's Language Skills: A Randomized Controlled Trial.

Purpose Research has indicated that interactive shared book reading can support a wide range of early language skills and that children who are read to regularly in the early years learn language faster, enter school with a larger vocabulary, and become more successful readers at school. Despite the large volume of research suggesting interactive shared reading is beneficial for language development, two fundamental issues remain outstanding: whether shared book reading interventions are equally effective (a) for children from all socioeconomic backgrounds and (b) for a range of language skills. Method To address these issues, we conducted a randomized controlled trial to investigate the effects of two 6-week interactive shared reading interventions on a range of language skills in children across the socioeconomic spectrum. One hundred and fifty children aged between 2;6 and 3;0 (years;months) were randomly assigned to one of three conditions: a pause reading, a dialogic reading, or an active shared reading control condition. Results The findings indicated that the interventions were effective at changing caregiver reading behaviors. However, the interventions did not boost children's language skills over and above the effect of an active reading control condition. There were also no effects of socioeconomic status. Conclusion This randomized controlled trial showed that caregivers from all socioeconomic backgrounds successfully adopted an interactive shared reading style. However, while the interventions were effective at increasing caregivers' use of interactive shared book reading behaviors, this did not have a significant impact on the children's language skills. The findings are discussed in terms of practical implications and future research. Supplemental Material https://doi.org/10.23641/asha.12420539

Schizophrenia-associated variation at <i>ZNF804A</i> correlates with altered experience-dependent dynamics of sleep slow waves and spindles in healthy young adults

The rs1344706 polymorphism in ZNF804A is robustly associated with schizophrenia and schizophrenia is, in turn, associated with abnormal non-rapid eye movement (NREM) sleep neurophysiology. To examine whether rs1344706 is associated with intermediate neurophysiological traits in the absence of disease, we assessed the relationship between genotype, sleep neurophysiology, and sleep-dependent memory consolidation in healthy participants. We recruited healthy adult males with no history of psychiatric disorder from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort. Participants were homozygous for either the schizophrenia-associated 'A' allele (N = 22) or the alternative 'C' allele (N = 18) at rs1344706. Actigraphy, polysomnography (PSG) and a motor sequence task (MST) were used to characterize daily activity patterns, sleep neurophysiology and sleep-dependent memory consolidation. Average MST learning and sleep-dependent performance improvements were similar across genotype groups, albeit more variable in the AA group. During sleep after learning, CC participants showed increased slow-wave (SW) and spindle amplitudes, plus augmented coupling of SW activity across recording electrodes. SW and spindles in those with the AA genotype were insensitive to learning, whilst SW coherence decreased following MST training. Accordingly, NREM neurophysiology robustly predicted the degree of overnight motor memory consolidation in CC carriers, but not in AA carriers. We describe evidence that rs1344706 polymorphism in ZNF804A is associated with changes in the coordinated neural network activity that supports offline information processing during sleep in a healthy population. These findings highlight the utility of sleep neurophysiology in mapping the impacts of schizophrenia-associated common genetic variants on neural circuit oscillations and function

The role of microRNA-binding site polymorphisms in DNA repair genes as risk factors for bladder cancer and breast cancer and their impact on radiotherapy outcomes

MicroRNAs (miRNAs) are involved in post-transcriptional regulation of gene expression through binding to messenger RNAs (mRNA) thereby promoting mRNA degradation or altered translation. A single-nucleotide polymorphism (SNP) located within a miRNA-binding site could thus alter mRNA translation and influence cancer risk and treatment response. The common SNPs located within the 3′-untranslated regions of 20 DNA repair genes were analysed for putative miRNA-binding sites using bioinformatics algorithms, calculating the difference in Gibbs free binding energy (ΔΔG) for each wild-type versus variant allele. Seven SNPs were selected to be genotyped in germ line DNAs both from a bladder cancer case–control series (752 cases and 704 controls) and 202 muscle-invasive bladder cancer radiotherapy cases. The PARP-1 SNP rs8679 was also genotyped in a breast cancer case–control series (257 cases and 512 controls). Without adjustment for multiple testing, multivariate analysis demonstrated an association with increased bladder cancer risk with PARP1 rs8679 (Ptrend = 0.05) while variant homozygotes of PARP1 rs8679 were also noted to have an increased breast cancer risk (P = 0.03). In the radiotherapy cases, carriers of the RAD51 rs7180135 minor allele had improved cancer-specific survival (hazard ratio 0.52, 95% confidence interval 0.31–0.87, P = 0.01). This is the first report of associations between DNA repair gene miRNA-binding site SNPs with bladder and breast cancer risk and radiotherapy outcomes. If validated, these findings may give further insight into the biology of bladder carcinogenesis, allow testing of the RAD51 SNP as a potential predictive biomarker and also reveal potential targets for new cancer treatments

RivFishTIME: A global database of fish time-series as a currency for global change ecology research in riverine systems

Motivation We compiled a global database of long-term riverine fish surveys from 46 regional and national monitoring programmes and from individual academic research efforts, with which numerous basic and applied questions in ecology and global change research can be explored. Such spatially and temporally extensive datasets have been lacking for freshwater systems in comparison to terrestrial ones. Main types of variables contained The database includes 11,386 time-series of riverine fish community catch data, including 646,270 species-specific abundance records, together with metadata related to the geographical location and sampling methodology of each time-series. Spatial location and grain The database contains 11,072 unique sampling locations (stream reach), spanning 19 countries, five biogeographical realms and 402 hydrographical basins world-wide. Time period and grain The database encompasses the period 1951–2019. Each time-series is composed of a minimum of two yearly surveys (mean = 8 years) and represents a minimum time span of 10 years (mean = 19 years). Major taxa and level of measurement The database includes 944 species of ray-finned fishes (Class Actinopterygii). Software format csv. Main conclusion Our collective effort provides the most comprehensive long-term community database of riverine fishes to date. This unique database should interest ecologists who seek to understand the impacts of human activities on riverine fish biodiversity and to model and predict how fish communities will respond to future environmental change. Together, we hope it will promote advances in macroecological research in the freshwater realm

Sub-arcsecond imaging of SiO in the HH 211 protostellar jet

We present images of the HH 211 molecular jet in the SiO v=0, J=1-0 line at 43 GHz made with the Very Large Array at approximately 0.5 arcsec resolution. The SiO emission appears to trace primarily internal bowshocks in the outflow, suggesting that the dust and molecular gas are accelerated via prompt entrainment at internal working surfaces in the jet. There is also some evidence for limb-brightening of the SiO emission, indicating that SiO emission may also arise from entrainment in the jet's boundary layer. Excitation temperatures of >~150-200 K are inferred from the SiO emission. Enhancements in the SiO abundance of ~10^6 over interstellar values are observed, and the possible origin of the SiO is discussed.Comment: 14 pages, 4 figures. Needs aastex, epsfig, times.sty. To appear in the Astrophysical Journal, July 200

Deficient Pms2, ERCC1, Ku86, CcOI in Field Defects During Progression to Colon Cancer

In carcinogenesis, the "field defect" is recognized clinically because of the high propensity of survivors of certain cancers to develop other malignancies of the same tissue type, often in a nearby location. Such field defects have been indicated in colon cancer. The molecular abnormalities that are responsible for a field defect in the colon should be detectable at high frequency in the histologically normal tissue surrounding a colonic adenocarcinoma or surrounding an adenoma with advanced neoplasia (well on the way to a colon cancer), but at low frequency in the colonic mucosa from patients without colonic neoplasia

South Africa’s private wildlife ranches protect globally significant populations of wild ungulates

Reversing biodiversity loss is a global imperative that requires setting aside sufficient space for species. In South Africa, an estimated area of 20 million ha is under wildlife ranching, a form of private land enterprise that adopts wildlife-based land uses for commercial gain. This land has potential to contribute towards biodiversity conservation, but the extent to which this occurs has not been evaluated. Using structured questionnaires of 226 wildlife ranchers, we assessed how the sector contributes towards the conservation of ungulates and elephants (hereafter herbivores). Overall, 40 herbivore species were present across the sample, where individual ranches had a mean of 15.0 (± 4.8) species, 1.9 (± 1.5) threatened species, and 3.6 (± 3.1) extralimital species per property. In comparison to 54 state PAs, wildlife ranches had significantly higher species richness, more threatened species but more extralimital species when property/reserve size was controlled for. Ranches conducting trophy hunting had similar species richness and numbers of extralimital species per ha, but fewer threatened species when compared to ranches conducting ecotourism. We estimate that 4.66–7.25 million herbivores occur on ranches nationally, representing one of the few examples on earth where indigenous mammal populations are thriving and demonstrating how sustainable use can lead to rewilding. We discuss the potential negative impacts of widespread game fencing on landscape fragmentation and gene flow, as well as how the widespread occurrence of extralimital species may lead to hybridisation, biotic homogenisation, and changes to vegetation dynamics. Despite these challenges, commercial wildlife ranching offers a viable option for conserving large mammalian herbivore biodiversity.Supplementary File 1. Online resources 1 and 2.Supplementary File 2. Online resources 3 and 4.Supplementary File 3. Online resource 5.The Green Fund/Development Bank of South Africa.http://link.springer.com/journal/10531hj2022Centre for Veterinary Wildlife StudiesMammal Research InstituteProduction Animal StudiesZoology and Entomolog

High-Resolution Molecular Line Observations of the Environment of the Class 0 Source B1-IRS

In this work we present VLA observations of the NH3, CCS, and H2O maser emission at 1 cm from the star forming region B1-IRS (IRAS 03301+3057) with ~ 5" (=1750 AU) of angular resolution. CCS emission is distributed in three clumps around the central source. These clumps exhibit a velocity gradient from red- to blueshifted velocities toward B1-IRS, probably due to an interaction with the outflow from an embedded protostar. The outflow and its powering source are traced by a reflection nebula and an associated infrared point source detected in a 2MASS K-band image. We find that this infrared point source is associated with water maser emission distributed in an elongated structure (~ 450 AU size) along the major axis of the reflection nebula and tracing the base of the outflow of the region. Ammonia emission is extended and spatially anticorrelated with CCS. This is the first time that this kind of anticorrelation is observed in a star forming region with such a high angular resolution, and illustrates the importance of time-dependent chemistry on small spatial scales. The relatively large abundance of CCS with respect to ammonia, compared with other star forming regions, suggests an extreme youth for the B1-IRS object (<10E+5 yr). We suggest the possibility that CCS abundance is enhanced via shock-induced chemistry.Comment: 31 pages, 9 figures. Accepted by The Astrophysical Journa

ANO10 mutations cause ataxia and coenzyme Q₁₀ deficiency.

Inherited ataxias are heterogeneous disorders affecting both children and adults, with over 40 different causative genes, making molecular genetic diagnosis challenging. Although recent advances in next-generation sequencing have significantly improved mutation detection, few treatments exist for patients with inherited ataxia. In two patients with adult-onset cerebellar ataxia and coenzyme Q10 (CoQ10) deficiency in muscle, whole exome sequencing revealed mutations in ANO10, which encodes anoctamin 10, a member of a family of putative calcium-activated chloride channels, and the causative gene for autosomal recessive spinocerebellar ataxia-10 (SCAR10). Both patients presented with slowly progressive ataxia and dysarthria leading to severe disability in the sixth decade. Epilepsy and learning difficulties were also present in one patient, while retinal degeneration and cataract were present in the other. The detection of mutations in ANO10 in our patients indicate that ANO10 defects cause secondary low CoQ10 and SCAR10 patients may benefit from CoQ10 supplementation