Crisis of the Mythological? The Melting of the Polar Ice in Greenland in Alfred Döblin’s Berge Meere und Giganten

The novel Berge Meere und Giganten was written in 1924. I would like to focus my attention on the 7th book in the novel, whose title is Die Enteisung Grönlands (The Melting of the Polar Ice in Greenland). To begin with, I will give a short summary of what the novel is about. The project to melt Greenland's polar ice forms the culmination of a history of the whole of humanity running from the 20th century all the way until the 27th century. Using all their military and technological might, the heat of the Icelandic volcanoes is captured in solid form and transported by ship to the Arctic. With the help of a gigantic net, this heat is then unloaded on to Greenland, thus melting its ice. Greenland ‘strikes back' however, firstly by casting a magical spell. My central thesis is that Döblin`s Greenland fiction is about the destruction of the myth of Greenland and that this ultimately documents a crisis of the mythological itself.&nbsp

„Mann-Weiber“ im Technikstaat

Alfred Döblins Roman Berge Meere und Giganten (1924) phantasiert die zukünftige Entwicklung der westlichen Kontinente zwischen dem 20. und 27. Jahrhundert. Strukturiert wird der in neun Bücher unterteilte Text weniger durch eine geschlossene Handlung als vielmehr durch die beständige Variation eines Grundthemas. Volker Klotz hat dieses Thema auf die Formel „Mensch und Natur“ gebracht. Es steht jedoch in enger Verbindung zu einem zweiten Thema, nämlich dem von Männlichkeit und Weiblichkeit: Di..

Search for pair and single production of new heavy quarks that decay to a Z boson and a third-generation quark in pp collisions at √s = 8TeV with the ATLAS detector

A search is presented for the production of new heavy quarks that decay to a Z boson and a third-generation Standard Model quark. In the case of a new charge +2/3 quark (T), the decay targeted is T -> Zt, while the decay targeted for a new charge -1/3 quark (B) is B -> Zb. The search is performed with a dataset corresponding to 20.3 fb(-1) of p p collisions at root s = 8TeV recorded in 2012 with the ATLAS detector at the CERN Large Hadron Collider. Selected events contain a high transverse momentum Z boson candidate reconstructed from a pair of oppositely charged same-flavor leptons (electrons or muons), and are analyzed in two channels defined by the absence or presence of a third lepton. Hadronic jets, in particular those with properties consistent with the decay of a b-hadron, are also required to be present in selected events. Different requirements are made on the jet activity in the event in order to enhance the sensitivity to either heavy quark pair production mediated by the strong interaction, or single production mediated by the electroweak interaction. No significant excess of events above the Standard Model expectation is observed, and lower limits are derived on the mass of vector-like T and B quarks under various branching ratio hypotheses, as well as upper limits on the magnitude of electroweak coupling parameters

Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

Funder: NCI U24CA211006Abstract: The Cancer Genome Atlas (TCGA) and International Cancer Genome Consortium (ICGC) curated consensus somatic mutation calls using whole exome sequencing (WES) and whole genome sequencing (WGS), respectively. Here, as part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, which aggregated whole genome sequencing data from 2,658 cancers across 38 tumour types, we compare WES and WGS side-by-side from 746 TCGA samples, finding that ~80% of mutations overlap in covered exonic regions. We estimate that low variant allele fraction (VAF < 15%) and clonal heterogeneity contribute up to 68% of private WGS mutations and 71% of private WES mutations. We observe that ~30% of private WGS mutations trace to mutations identified by a single variant caller in WES consensus efforts. WGS captures both ~50% more variation in exonic regions and un-observed mutations in loci with variable GC-content. Together, our analysis highlights technological divergences between two reproducible somatic variant detection efforts