Rhyolitic tephra horizons in northwestern Europe and Iceland from the AD 700s-800s: a potential alternative for dating first human impact

The distribution and geochemistry of four rhyolitic tephra horizons from Iceland dated to the ad 700s–800s is assessed. These include the rhyolitic phase of the Landnám tephra (ad 870s), the ad 860 layer, a previously unrecorded tephra called the GA4–85 layer (c. ad 700–800) and the Tjïrnuvík tephra (c. ad 800s). The ad 860 and GA4–85 layers were first found in peat bogs in north Ireland. They are here correlated with equivalent horizons on Iceland which were found below the Landnám tephra (c. ad 870s). This time period is considered important in the North Atlantic region, because it coincides with a phase of human settlement in Iceland and the Faroe Islands. The establishment of a detailed tephrochronology may provide a tool for exact dating of sediment successions and sediments associated with archaeological excavations. Caution must be taken especially on Iceland where the Landnám tephra is often used for dating archaeological sites. This investigation show that several rhyolitic tephra horizons occur close in time to the Landnám tephra, and that mistakes can be made if detailed geochemical analyses are not carried out, especially in areas which are distal to the source of the Landnám tephra (the Veidivötn and Torfajökull volcanic systems, southern Iceland)

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

DNA methylation quantitative trait locus (mQTL) analyses on 32,851 participants identify genetic variants associated with DNA methylation at 420,509 sites in blood, resulting in a database of >270,000 independent mQTLs.Characterizing genetic influences on DNA methylation (DNAm) provides an opportunity to understand mechanisms underpinning gene regulation and disease. In the present study, we describe results of DNAm quantitative trait locus (mQTL) analyses on 32,851 participants, identifying genetic variants associated with DNAm at 420,509 DNAm sites in blood. We present a database of >270,000 independent mQTLs, of which 8.5% comprise long-range (trans) associations. Identified mQTL associations explain 15-17% of the additive genetic variance of DNAm. We show that the genetic architecture of DNAm levels is highly polygenic. Using shared genetic control between distal DNAm sites, we constructed networks, identifying 405 discrete genomic communities enriched for genomic annotations and complex traits. Shared genetic variants are associated with both DNAm levels and complex diseases, but only in a minority of cases do these associations reflect causal relationships from DNAm to trait or vice versa, indicating a more complex genotype-phenotype map than previously anticipated.Molecular Epidemiolog