Structure of the northwestern North Anatolian Fault Zone imaged via teleseismic scattering tomography

Information on fault zone structure is essential for our understanding of earthquake mechanics, continental deformation and seismic hazard. We use the scattered seismic wavefield to study the subsurface structure of the North Anatolian Fault Zone (NAFZ) in the region of the 1999 İzmit and Düzce ruptures using data from an 18-month dense deployment of seismometers with a nominal station spacing of 7 km. Using the forward- and back-scattered energy that follows the direct P-wave arrival from teleseismic earthquakes, we apply a scattered wave inversion approach and are able to resolve changes in lithospheric structure on a scale of 10 km or less in an area of about 130 km by 100 km across the NAFZ. We find several crustal interfaces that are laterally incoherent beneath the surface strands of the NAFZ and evidence for contrasting crustal structures either side of the NAFZ, consistent with the presence of juxtaposed crustal blocks and ancient suture zones. Although the two strands of the NAFZ in the study region strike roughly east–west, we detect strong variations in structure both north–south, across boundaries of the major blocks, and east–west, parallel to the strike of the NAFZ. The surface expression of the two strands of the NAFZ is coincident with changes on main interfaces and interface terminations throughout the crust and into the upper mantle in the tomographic sections. We show that a dense passive network of seismometers is able to capture information from the scattered seismic wavefield and, using a tomographic approach, to resolve the fine scale structure of crust and lithospheric mantle even in geologically complex regions. Our results show that major shear zones exist beneath the NAFZ throughout the crust and into the lithospheric mantle, suggesting a strong coupling of strain at these depths

Legal Aid in the Nordic Countries

The chapter serves as the introduction to the collection, and provides the background for, and overview of, the book. The goal of the collection is to examine and compare civil legal aid in the Nordic countries in relation to the welfare state. An introduction to the common background of the Nordic countries and their legal aid schemes is compared to international developments in the field. The Nordic legal aid research, mainly empirical research on ‘unmet legal needs’, is reviewed, indicating a current remaining unmet need for legal aid. This overview reviews the chapters on legal aid in the different Nordic countries (which serve to describe and analyse the national schemes), the case studies (which serve to develop on features and challenges of the public schemes), and a final section that serves to contextualise the studies of the Nordic schemes in a European and theoretical perspective

Epigenetic profiling of ADHD symptoms trajectories: a prospective, methylome-wide study.

Attention-deficit/hyperactivity disorder (ADHD) is a prevalent developmental disorder, associated with a range of long-term impairments. Variation in DNA methylation, an epigenetic mechanism, is implicated in both neurobiological functioning and psychiatric health. However, the potential role of DNA methylation in ADHD symptoms is currently unclear. In this study, we examined data from the Avon Longitudinal Study of Parents and Children (ALSPAC)-specifically the subsample forming the Accessible Resource for Integrated Epigenomics Studies (ARIES)-that includes (1) peripheral measures of DNA methylation (Illumina 450k) at birth (n=817, 49% male) and age 7 (n=892, 50% male) and (2) trajectories of ADHD symptoms (7-15 years). We first employed a genome-wide analysis to test whether DNA methylation at birth associates with later ADHD trajectories; and then followed up at age 7 to investigate the stability of associations across early childhood. We found that DNA methylation at birth differentiated ADHD trajectories across multiple genomic locations, including probes annotated to SKI (involved in neural tube development), ZNF544 (previously implicated in ADHD), ST3GAL3 (linked to intellectual disability) and PEX2 (related to perixosomal processes). None of these probes maintained an association with ADHD trajectories at age 7. Findings lend novel insights into the epigenetic landscape of ADHD symptoms, highlighting the potential importance of DNA methylation variation in genes related to neurodevelopmental and peroxisomal processes that play a key role in the maturation and stability of cortical circuits.This article is freely available via Open Access. Click on the Additional Link above to access the full tex