Hemispheric asymmetry in the sunspot cycle as a nonextensive phenomenon

The appearance of dark sunspots over the solar photosphere is not considered to be symmetric between the northern and southern hemispheres. Among the different conclusions obtained by several authors, we can point out that the North-South asymmetry is a real and systematic phenomenon and is not due to random variability. In the present work, we selected the sunspot area data of a sample of 13 solar cycles divided by hemisphere extracted from the Marshall Space Flight Centre (MSFC) database to investigate the behavior of probability distributions using an out-of-equilibrium statistical model a.k.a non-extensive statistical mechanics. Based on this statistical framework, we obtained that the non-extensive entropic parameter $q$ has a semi-sinusoidal variation with a period of $\sim$22 year (Hale cycle). Among the most important results, we can highlight that the asymmetry index $q(A)$ revealed the dominance of the northern hemisphere against the southern one. Thus, we concluded that the parameter $q(A)$ can be considered an effective measure for diagnosing long-term variations of the solar dynamo. Finally, our study opens a new approach to investigating solar variability from the nonextensive perspective.Comment: 17 pages, 2 tables and 5 figures. Submitted to Solar Physic

Finishing the euchromatic sequence of the human genome

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead