SHRIMP U–Pb zircon dating of anatexis in high-grade migmatite complexes of Central Spain: implications in the Hercynian evolution of Central Iberia

U–Pb SHRIMP ages obtained in zircons from the Sotosalbos and Toledo anatectic complexes in Central Spain give new constraints to the evolution of the inner part of the Hercynian Iberian belt. Pre- Hercynian ages in zircons from the Sotosalbos complex (~464 Ma) are well preserved and reveal that an age diversity of the Lower Paleozoic magmatism in the area exists, as previous data on westernmost orthogneisses yield significant older ages. Zircon ages in the pelite-derived granites from the Toledo complex also show an important Neoproterozoic age component which points to a metasedimentary protolith deposited maximally 560 Ma ago. Younger zircon populations in both complexes at ~330 Ma in the Sotosalbos region and ~317 Ma in the Toledo complex indicate an important diachronism between the anatectic processes in both areas but also that these processes are mainly unrelated to the generation of the later Hercynian granite batholith of Central Spain, which could be of deeper crustal derivation. In addition, as migmatization occurred late in the metamorphic cycle, after peak conditions were attained, the age of anatexis is younger than the age of the main Hercynian metamorphic event, which still is not well constrained

Libert Froidmont’s conception and imagination of space in three early works: Peregrinatio cœlestis (1616), De cometa (1618), Meteorologica (1627)

International audienc

Neuronal subtypes and diversity revealed by single-nucleus RNA sequencing of the human brain

The human brain has enormously complex cellular diversity and connectivities fundamental to our neural functions, yet difficulties in interrogating individual neurons has impeded understanding of the underlying transcriptional landscape. We developed a scalable approach to sequence and quantify RNA molecules in isolated neuronal nuclei from post-mortem brain, generating 3,227 sets of single neuron data from six distinct regions of the cerebral cortex. Using an iterative clustering and classification approach, we identified 16 neuronal subtypes that were further annotated on the basis of known markers and cortical cytoarchitecture. These data demonstrate a robust and scalable method for identifying and categorizing single nuclear transcriptomes, revealing shared genes sufficient to distinguish novel and orthologous neuronal subtypes as well as regional identity within the human brain

Perspectives on ENCODE

The Encylopedia of DNA Elements (ENCODE) Project launched in 2003 with the long-term goal of developing a comprehensive map of functional elements in the human genome. These included genes, biochemical regions associated with gene regulation (for example, transcription factor binding sites, open chromatin, and histone marks) and transcript isoforms. The marks serve as sites for candidate cis-regulatory elements (cCREs) that may serve functional roles in regulating gene expression1. The project has been extended to model organisms, particularly the mouse. In the third phase of ENCODE, nearly a million and more than 300,000 cCRE annotations have been generated for human and mouse, respectively, and these have provided a valuable resource for the scientific community.11Nsciescopu