Structure symmetry determination and magnetic evolution in Sr2Ir1−xRhxO4\rm Sr_2Ir_{1-x}Rh_{x}O_4

We use single-crystal neutron diffraction to determine the crystal structure symmetry and the magnetic evolution in the rhodium doped iridates $\rm Sr_2Ir_{1-x}Rh_{x}O_4$ ($0\leq x \leq 0.16$). Throughout this doping range, the crystal structure retains a tetragonal symmetry (space group $I4_1/a$) with two distinct magnetic Ir sites in the unit cell forming staggered $\rm IrO_6$ rotation. Upon Rh doping, the magnetic order is suppressed and the magnetic moment of Ir$^{4+}$ is reduced from 0.21 $\rm \mu_B$/Ir for $x=0$ to 0.18 $\rm \mu_B$/Ir for $x=0.12$. The magnetic structure at $x=0.12$ is different from that of the parent compound while the moments remain in the basal plane.Comment: Accepted for publication in Phys. Rev.

Structure Symmetry Determination and Magnetic Evolution in Sr\u3csub\u3e2\u3c/sub\u3eIr\u3csub\u3e1−\u3cem\u3ex\u3c/em\u3e\u3c/sub\u3eRh\u3csub\u3e\u3cem\u3ex\u3c/em\u3e\u3c/sub\u3eO\u3csub\u3e4\u3c/sub\u3e

We use single-crystal neutron diffraction to determine the crystal structure symmetry and the magnetic evolution in the rhodium-doped iridates Sr2Ir1−xRhxO4 (0≤ x ≤ 0.16). Throughout this doping range, the crystal structure retains a tetragonal symmetry (space group I41/a) with two distinct magnetic Ir sites in the unit cell forming staggered IrO6 rotation. Upon Rh doping, the magnetic order is suppressed and the magnetic moment of Ir4+ is reduced from 0.21μB/Ir for x=0 to 0.18μB/Ir for x=0.12. The magnetic structure at x=0.12 is different from that of the parent compound, while the moments remain in the basal plane

Effect of childhood victimization on occupational prestige and income trajectories

Background Violence toward children (childhood victimization) is a major public health problem, with long-term consequences on economic well-being. The purpose of this study was to determine whether childhood victimization affects occupational prestige and income in young adulthood. We hypothesized that young adults who experienced more childhood victimizations would have less prestigious jobs and lower incomes relative to those with no victimization history. We also explored the pathways in which childhood victimization mediates the relationships between background variables, such as parent’s educational impact on the socioeconomic transition into adulthood. Methods A nationally representative sample of 8,901 young adults aged 18–28 surveyed between 1999–2009 from the National Longitudinal Survey of Youth 1997 (NLSY) were analyzed. Covariate-adjusted multivariate linear regression and path models were used to estimate the effects of victimization and covariates on income and prestige levels and on income and prestige trajectories. After each participant turned 18, their annual 2002 Census job code was assigned a yearly prestige score based on the 1989 General Social Survey, and their annual income was calculated via self-reports. Occupational prestige and annual income are time-varying variables measured from 1999–2009. Victimization effects were tested for moderation by sex, race, and ethnicity in the multivariate models. Results Approximately half of our sample reported at least one instance of childhood victimization before the age of 18. Major findings include 1) childhood victimization resulted in slower income and prestige growth over time, and 2) mediation analyses suggested that this slower prestige and earnings arose because victims did not get the same amount of education as non-victims. Conclusions Results indicated that the consequences of victimization negatively affected economic success throughout young adulthood, primarily by slowing the growth in prosperity due to lower education levels

Monarch Butterfly Conservation Through the Social Lens: Eliciting Public Preferences for Management Strategies Across Transboundary Nations

The monarch butterfly (Danaus plexippus), an iconic species that migrates annually across North America, has steeply declined in numbers over the past decade. Across the species\u27 range, public, private, and non-profit organizations aim to reverse the monarch decline by engaging in conservation activities such as habitat restoration, larvae monitoring, and butterfly tagging. Urban residents can actively participate in these activities, yet their contribution can also be realized as an electorate body able to influence the design of conservation programs according to their interests. Little is known, however about their preferences toward the objectives and design of international monarch conservation policies. In this paper, we investigate these preferences via a survey design using Discrete Choice Experiments (DCEs) and Latent Class Analysis (LC) of urban residents across the main eastern migratory flyway in Ontario, Canada, and the eastern United States. Attributes in the DCE included the size and trend of overwintering butterfly colonies, the type of institution leading the conservation program, international allocation of funds, and the percentage of funds dedicated to research. From the general populace, we isolated respondents already engaged in monarch conservation activities to explore how they compare. We sent a smaller set of surveys deliberately withholding the expected-success forecast of the monarch recovery program to assess the value of information for urban residents within a conservation context. The LC distinguished three groups of respondents among urban residents: (1) the main group, labeled “Eager,” accounting for 72.4% of the sample, that showed a high potential for supporting conservation policies and had remarkable similarities with the monarch enthusiasts\u27 sample; (2) a “Pro Nation” group (18.4%) marked by their increased willingness to support conservation initiatives solely focused within their country of residence; and (3) an “Opinionated” segment (9.23%), that was highly reactive to changes of the leading institution, resources allocation, and economic contribution proposed. Key findings from this research reveal that to maximize potential support amongst urban residents in the monarch\u27s breeding range, a conservation strategy for the monarch butterfly should be led by not-for-profit organizations, should strive for transboundary cooperation, and should include the communication of anticipated ecological outcomes

Ageing-associated DNA methylation dynamics are a molecular readout of lifespan variation among mammalian species.

BACKGROUND: Mammalian species exhibit a wide range of lifespans. To date, a robust and dynamic molecular readout of these lifespan differences has not yet been identified. Recent studies have established the existence of ageing-associated differentially methylated positions (aDMPs) in human and mouse. These are CpG sites at which DNA methylation dynamics show significant correlations with age. We hypothesise that aDMPs are pan-mammalian and are a dynamic molecular readout of lifespan variation among different mammalian species. RESULTS: A large-scale integrated analysis of aDMPs in six different mammals reveals a strong negative relationship between rate of change of methylation levels at aDMPs and lifespan. This relationship also holds when comparing two different dog breeds with known differences in lifespans. In an ageing cohort of aneuploid mice carrying a complete copy of human chromosome 21, aDMPs accumulate far more rapidly than is seen in human tissues, revealing that DNA methylation at aDMP sites is largely shaped by the nuclear trans-environment and represents a robust molecular readout of the ageing cellular milieu. CONCLUSIONS: Overall, we define the first dynamic molecular readout of lifespan differences among mammalian species and propose that aDMPs will be an invaluable molecular tool for future evolutionary and mechanistic studies aimed at understanding the biological factors that determine lifespan in mammals

Community-curated and standardised metadata of published ancient metagenomic samples with AncientMetagenomeDir

Ancient DNA and RNA are valuable data sources for a wide range of disciplines. Within the field of ancient metagenomics, the number of published genetic datasets has risen dramatically in recent years, and tracking this data for reuse is particularly important for large-scale ecological and evolutionary studies of individual taxa and communities of both microbes and eukaryotes. AncientMetagenomeDir (archived at https://doi.org/10.5281/zenodo.3980833) is a collection of annotated metagenomic sample lists derived from published studies that provide basic, standardised metadata and accession numbers to allow rapid data retrieval from online repositories. These tables are community-curated and span multiple sub-disciplines to ensure adequate breadth and consensus in metadata definitions, as well as longevity of the database. Internal guidelines and automated checks facilitate compatibility with established sequence-read archives and term-ontologies, and ensure consistency and interoperability for future meta-analyses. This collection will also assist in standardising metadata reporting for future ancient metagenomic studies

Positive and Negative Parenting in Conduct Disorder with High versus Low Levels of Callous-Unemotional Traits

Less is known about the relationship between conduct disorder (CD), callous-unemotional (CU) traits and positive and negative parenting in adolescence compared to early childhood. We combined traditional univariate analyses with a novel machine learning classifier (Angle-based Generalised Matrix Learning Vector Quantisation) to classify youth (N = 756; 9-18 years) into typically-developing (TD) or CD groups with or without elevated CU traits (CD/HCU, CD/LCU respectively) using youth- and parent-report measures of parenting behaviour. At the group level, both CD/HCU and CD/LCU were associated with high negative and low positive parenting relative to TD. However, only positive parenting differed between the CD/HCU and CD/LCU groups. In classification analyses, performance was best when distinguishing CD/HCU from TD groups and poorest when distinguishing CD/HCU from CD/LCU groups. Positive and negative parenting were both relevant when distinguishing CD/HCU from TD, negative parenting was most relevant when distinguishing between CD/LCU from TD, and positive parenting was most relevant when distinguishing CD/HCU from CD/LCU groups. These findings suggest that while positive parenting distinguishes between CD/HCU and CD/LCU, negative parenting is associated with both CD subtypes. These results highlight the importance of considering multiple parenting behaviours in CD with varying levels of CU traits in late childhood or adolescence

Individual common variants exert weak effects on the risk for autism spectrum disorders.

While it is apparent that rare variation can play an important role in the genetic architecture of autism spectrum disorders (ASDs), the contribution of common variation to the risk of developing ASD is less clear. To produce a more comprehensive picture, we report Stage 2 of the Autism Genome Project genome-wide association study, adding 1301 ASD families and bringing the total to 2705 families analysed (Stages 1 and 2). In addition to evaluating the association of individual single nucleotide polymorphisms (SNPs), we also sought evidence that common variants, en masse, might affect the risk. Despite genotyping over a million SNPs covering the genome, no single SNP shows significant association with ASD or selected phenotypes at a genome-wide level. The SNP that achieves the smallest P-value from secondary analyses is rs1718101. It falls in CNTNAP2, a gene previously implicated in susceptibility for ASD. This SNP also shows modest association with age of word/phrase acquisition in ASD subjects, of interest because features of language development are also associated with other variation in CNTNAP2. In contrast, allele scores derived from the transmission of common alleles to Stage 1 cases significantly predict case status in the independent Stage 2 sample. Despite being significant, the variance explained by these allele scores was small (Vm< 1%). Based on results from individual SNPs and their en masse effect on risk, as inferred from the allele score results, it is reasonable to conclude that common variants affect the risk for ASD but their individual effects are modest