El Sistema Nacional de Investigadores en 2009 : un vector para la internacionalización de las élites científicas ?

In this paper the authors expect to analyze the following hypothesis from different angles: the National Researchers System (Sistema Nacional de Investigadores, SNI) has created a standardization, progressive although incomplete, of the criteria governing the national scientific elite based on the criteria that prevail amongst the so-called developed countries. We study some of the indicators following which the SNI members who belong to the most aged groups present obvious differences with regard to the less aged ones and are a symptom of this homogenization dynamics, like, for instance, the age at which the doctorate degree is obtained. We also analyze the distortions that characterize this universe, like v.g. the fact that women are under-represented. A systematic analysis of the 2009 data about the SNI researchers, together with a sample of academic trajectories taken from the CVU (Joint Curriculum Vitae, Curriculum vitae único) helps us to show at what extent obtaining a degree in a foreign country helps to achieve a rapid career progression within the system, emphasizing the slants by disciplinary area and additional factors that allow to explain how they can get a high scientific prestige capital

A new look at the cosmic ray positron fraction

The positron fraction in cosmic rays was found to be a steadily increasing in function of energy, above $\sim$ 10 GeV. This behaviour contradicts standard astrophysical mechanisms, in which positrons are secondary particles, produced in the interactions of primary cosmic rays during the propagation in the interstellar medium. The observed anomaly in the positron fraction triggered a lot of excitement, as it could be interpreted as an indirect signature of the presence of dark matter species in the Galaxy. Alternatively, it could be produced by nearby astrophysical sources, such as pulsars. Both hypotheses are probed in this work in light of the latest AMS-02 positron fraction measurements. The transport of the primary and secondary positrons in the Galaxy is described using a semi-analytic two-zone model. MicrOMEGAs is used to model the positron flux generated by dark matter species. The description of the positron fraction from astrophysical sources is based on the pulsar observations included in the ATNF catalogue. We find that the mass of the favoured dark matter candidates is always larger than 500 GeV. The only dark matter species that fulfils the numerous gamma ray and cosmic microwave background bounds is a particle annihilating into four leptons through a light scalar or vector mediator, with a mixture of tau (75%) and electron (25%) channels, and a mass between 0.5 and 1 TeV. The positron anomaly can also be explained by a single astrophysical source and a list of five pulsars from the ATNF catalogue is given. Those results are obtained with the cosmic ray transport parameters that best fit the B/C ratio. Uncertainties in the propagation parameters turn out to be very significant. In the WIMP annihilation cross section to mass plane for instance, they overshadow the error contours derived from the positron data.Comment: 20 pages, 16 figures, accepted for publication in A&A, corresponds to published versio

Variety of idempotents in nonassociative algebras

In this paper, we study the variety of all nonassociative (NA) algebras from the idempotent point of view. We are interested, in particular, in the spectral properties of idempotents when algebra is generic, i.e. idempotents are in general position. Our main result states that in this case, there exist at least $n-1$ nontrivial obstructions (syzygies) on the Peirce spectrum of a generic NA algebra of dimension $n$. We also discuss the exceptionality of the eigenvalue $\lambda=\frac12$ which appears in the spectrum of idempotents in many classical examples of NA algebras and characterize its extremal properties in metrised algebras.Comment: 27 pages, 1 figure, submitte

A local-global principle for linear dependence of noncommutative polynomials

A set of polynomials in noncommuting variables is called locally linearly dependent if their evaluations at tuples of matrices are always linearly dependent. By a theorem of Camino, Helton, Skelton and Ye, a finite locally linearly dependent set of polynomials is linearly dependent. In this short note an alternative proof based on the theory of polynomial identities is given. The method of the proof yields generalizations to directional local linear dependence and evaluations in general algebras over fields of arbitrary characteristic. A main feature of the proof is that it makes it possible to deduce bounds on the size of the matrices where the (directional) local linear dependence needs to be tested in order to establish linear dependence.Comment: 8 page

Free-running L-band VCSEL for 1.25 Gbps hybrid radio-fiber cloud optical interconnects

International audienceWe demonstrate a free-running directly-modulated 1580 nm VCSEL suitable for hybrid wireless/optical interconnects supporting cloud data centers. Error-free transmission at 1.25 Gbps was achieved after 6.5 GHz wireless link and 1 km bend-insensitive fiber

β blockers and mortality after myocardial infarction in patients without heart failure: multicentre prospective cohort study

Objective: To assess the association between early and prolonged β blocker treatment and mortality after acute myocardial infarction. Design: Multicentre prospective cohort study. Setting: Nationwide French registry of Acute ST- and non-ST-elevation Myocardial Infarction (FAST-MI) (at 223 centres) at the end of 2005. Participants: 2679 consecutive patients with acute myocardial infarction and without heart failure or left ventricular dysfunction. Main outcome measures: Mortality was assessed at 30 days in relation to early use of β blockers (≤48 hours of admission), at one year in relation to discharge prescription, and at five years in relation to one year use. Results: β blockers were used early in 77% (2050/2679) of patients, were prescribed at discharge in 80% (1783/2217), and were still being used in 89% (1230/1383) of those alive at one year. Thirty day mortality was lower in patients taking early β blockers (adjusted hazard ratio 0.46, 95% confidence interval 0.26 to 0.82), whereas the hazard ratio for one year mortality associated with β blockers at discharge was 0.77 (0.46 to 1.30). Persistence of β blockers at one year was not associated with lower five year mortality (hazard ratio 1.19, 0.65 to 2.18). In contrast, five year mortality was lower in patients continuing statins at one year (hazard ratio 0.42, 0.25 to 0.72) compared with those discontinuing statins. Propensity score and sensitivity analyses showed consistent results. Conclusions: Early β blocker use was associated with reduced 30 day mortality in patients with acute myocardial infarction, and discontinuation of β blockers at one year was not associated with higher five year mortality. These findings question the utility of prolonged β blocker treatment after acute myocardial infarction in patients without heart failure or left ventricular dysfunction. Trial registration: Clinical trials NCT00673036

Increased frequency of the immunoglobulin enhancer HS1,2 allele 2 in coeliac disease

Background: Coeliac disease ( CD) is characterized by increased immunological responsiveness to ingested gliadin in genetically predisposed individuals. This genetic predisposition is not completely defined. A dysregulation of immunoglobulins (Ig) is present in CD: since antiendomysium antibodies (anti-EMA) are of the IgA class. One polymorphic enhancer within the locus control region (LCR) of the immunoglobulin heavy chain cluster at the 3' of the C alpha-1 gene was investigated. The correlation of the penetrance of the four different alleles of the HS1,2-A enhancer of the LCR-1 3' to C alpha-1 in CD patients compared to a control population was analysed. Methods: A total of 115 consecutive CD outpatients, on a gluten-free diet, and 248 healthy donors, age- and sex-matched, from the same geographical area were enrolled in the study. HS1,2-A allele frequencies were investigated by nested polymerase chain reaction (PCR). Results: The frequency of allele 2 of the enhancer HS1,2-A gene was increased by 30.8% as compared to the control frequency. The frequency of homozygosity for allele 2 was significantly increased in CD patients. Crude odds ratio ( OR) showed that those with 2/2 and 2/4 ( OR 2.63, P < 0.001 and OR 2.01, P = 0.03) have a significantly higher risk of developing the disease. In contrast, allele 1/2 may represent a protective genetic factor against CD ( OR 0.52, P = 0.01). Conclusions: These data provide further evidence of a genetic predisposition in CD. Because of the Ig dysregulation in CD, the enhancer HS1,2-A may be involved in the pathogenesis

Position and sequence conservation in Amniota of polymorphic enhancer HS1.2 within the palindrome of IgH 3'Regulatory Region

<p>Abstract</p> <p>Background</p> <p>The Immunoglobulin heavy chain (IgH) 3' Regulatory Region (3'RR), located at the 3' of the constant alpha gene, plays a crucial role in immunoglobulin production. In humans, there are 2 copies of the 3'RR, each composed of 4 main elements: 3 enhancers and a 20 bp tandem repeat. The single mouse 3'RR differs from the two human ones for the presence of 4 more regulative elements with the double copy of one enhancer at the border of a palindromic region.</p> <p>Results</p> <p>We compared the 3'RR organization in genomes of vertebrates to depict the evolutionary history of the region and highlight its shared features. We found that in the 8 species in which the whole region was included in a fully assembled contig (mouse, rat, dog, rabbit, panda, orangutan, chimpanzee, and human), the shared elements showed synteny and a highly conserved sequence, thus suggesting a strong evolutionary constraint. In these species, the wide 3'RR (~30 kb in human) bears a large palindromic sequence, consisting in two ~3 kb complementary branches spaced by a ~3 kb sequence always including the HS1.2 enhancer. In mouse and rat, HS3 is involved by the palindrome so that one copy of the enhancer is present on each side. A second relevant feature of our present work concerns human polymorphism of the HS1.2 enhancer, associated to immune diseases in our species. We detected a similar polymorphism in all the studied Catarrhini (a primate parvorder). The polymorphism consists of multiple copies of a 40 bp element up to 12 in chimpanzees, 8 in baboons, 6 in macaque, 5 in gibbons, 4 in humans and orangutan, separated by stretches of Cytosine. We show specific binding of this element to nuclear factors.</p> <p>Conclusions</p> <p>The nucleotide sequence of the palindrome is not conserved among evolutionary distant species, suggesting pressures for the maintenance of two self-matching regions driving a three-dimensional structure despite of the inter-specific divergence at sequence level. The information about the conservation of the palindromic structure and the settling in primates of the polymorphic feature of HS1.2 show the relevance of these structures in the control and modulation of the Ig production through the formation of possible three-dimensional structures.</p