2,577 research outputs found
Strategy updating rules and strategy distributions in dynamical multiagent systems
In the evolutionary version of the minority game, agents update their
strategies (gene-value ) in order to improve their performance. Motivated by
recent intriguing results obtained for prize-to-fine ratios which are smaller
than unity, we explore the system's dynamics with a strategy updating rule of
the form (). We find that the strategy
distribution depends strongly on the values of the prize-to-fine ratio , the
length scale , and the type of boundary condition used. We show that
these parameters determine the amplitude and frequency of the the temporal
oscillations observed in the gene space. These regular oscillations are shown
to be the main factor which determines the strategy distribution of the
population. In addition, we find that agents characterized by
(a coin-tossing strategy) have the best chances of survival at asymptotically
long times, regardless of the value of and the boundary conditions
used.Comment: 4 pages, 7 figure
New Superhard Phases for 3D C60-based Fullerites
We have explored new possible phases of 3D C60-based fullerites using
semiempirical potentials and ab-initio density functional methods. We have
found three closely related structures - two body centered orthorhombic and one
body centered cubic - having 52, 56 and 60 tetracoordinated atoms per molecule.
These 3D polymers result in semiconductors with bulk moduli near 300 GPa, and
shear moduli around 240 GPa, which make them good candidates for new low
density superhard materials.Comment: To be published in Physical Review Letter
Consistency between ARPES and STM measurements on SmB
Strongly correlated topological surface states are promising platforms for
next-generation quantum applications, but they remain elusive in real
materials. The correlated Kondo insulator SmB is one of the most promising
candidates, with theoretically predicted heavy Dirac surface states supported
by transport and scanning tunneling microscopy (STM) experiments. However, a
puzzling discrepancy appears between STM and angle-resolved photoemission
(ARPES) experiments on SmB. Although ARPES detects spin-textured surface
states, their velocity is an order of magnitude higher than expected, while the
Dirac point -- the hallmark of any topological system -- can only be inferred
deep within the bulk valence band. A significant challenge is that SmB
lacks a natural cleavage plane, resulting in ordered surface domains limited to
10s of nanometers. Here we use STM to show that surface band bending can shift
energy features by 10s of meV between domains. Starting from our STM spectra,
we simulate the full spectral function as an average over multiple domains with
different surface potentials. Our simulation shows excellent agreement with
ARPES data, and thus resolves the apparent discrepancy between large-area
measurements that average over multiple band-shifted domains and
atomically-resolved measurements within a single domain
Solos do campo experimental da Embrapa Algodão, em Patos-PB: levantamento detalhado e potencial edáfico.
bitstream/CNPS/11833/1/bpd17_2002_patos_pb.pd
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Promotion of Mn(II) Oxidation and Remediation of Coal Mine Drainage in Passive Treatment Systems by Diverse Fungal and Bacterial Communities
Biologically active, passive treatment systems are commonly employed for removing high concentrations of dissolved Mn(II) from coal mine drainage (CMD). Studies of microbial communities contributing to Mn attenuation through the oxidation of Mn(II) to sparingly soluble Mn(III/IV) oxide minerals, however, have been sparse to date. This study reveals a diverse community of Mn(II)-oxidizing fungi and bacteria existing in several CMD treatment systems.Organismic and Evolutionary Biolog
Whole exome sequencing of extreme morbid obesity patients: translational implications for obesity and related disorders
Whole-exome sequencing (WES) is a new tool that allows the rapid, inexpensive and accurate exploration of Mendelian and complex diseases, such as obesity. To identify sequence variants associated with obesity, we performed WES of family trios of one male teenager and one female child with severe early-onset obesity. Additionally, the teenager patient had hypopituitarism and hyperprolactinaemia. A comprehensive bioinformatics analysis found de novo and compound heterozygote sequence variants with a damaging effect on genes previously associated with obesity in mice (LRP2) and humans (UCP2), among other intriguing mutations affecting ciliary function (DNAAF1). A gene ontology and pathway analysis of genes harbouring mutations resulted in the significant identification of overrepresented pathways related to ATP/ITP (adenosine/inosine triphosphate) metabolism and, in general, to the regulation of lipid metabolism. We discuss the clinical and physiological consequences of these mutations and the importance of these findings for either the clinical assessment or eventual treatment of morbid obesity.Gilberto Paz-Filho, Margaret C.S. Boguszewski, Claudio A. Mastronardi, Hardip R. Patel, Angad S. Johar, Aaron Chuah, Gavin A. Huttley, Cesar L. Boguszewski, Ma-Li Wong, Mauricio Arcos-Burgos and Julio Licini
Electrophysiological Heterogeneity of Fast-Spiking Interneurons: Chandelier versus Basket Cells
In the prefrontal cortex, parvalbumin-positive inhibitory neurons play a prominent role in the neural circuitry that subserves working memory, and alterations in these neurons contribute to the pathophysiology of schizophrenia. Two morphologically distinct classes of parvalbumin neurons that target the perisomatic region of pyramidal neurons, chandelier cells (ChCs) and basket cells (BCs), are generally thought to have the same "fast-spiking" phenotype, which is characterized by a short action potential and high frequency firing without adaptation. However, findings from studies in different species suggest that certain electrophysiological membrane properties might differ between these two cell classes. In this study, we assessed the physiological heterogeneity of fast-spiking interneurons as a function of two factors: species (macaque monkey vs. rat) and morphology (chandelier vs. basket). We showed previously that electrophysiological membrane properties of BCs differ between these two species. Here, for the first time, we report differences in ChCs membrane properties between monkey and rat. We also found that a number of membrane properties differentiate ChCs from BCs. Some of these differences were species-independent (e.g., fast and medium afterhyperpolarization, firing frequency, and depolarizing sag), whereas the differences in the first spike latency between ChCs and BCs were species-specific. Our findings indicate that different combinations of electrophysiological membrane properties distinguish ChCs from BCs in rodents and primates. Such electrophysiological differences between ChCs and BCs likely contribute to their distinctive roles in cortical circuitry in each species. © 2013 Povysheva et al
A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD
In previous studies of a genetic isolate, we identified significant linkage of attention deficit hyperactivity disorder (ADHD) to 4q, 5q, 8q, 11q and 17p. The existence of unique large size families linked to multiple regions, and the fact that these families came from an isolated population, we hypothesized that two-locus interaction contributions to ADHD were plausible. Several analytical models converged to show significant interaction between 4q and 11q (P<1 × 10−8) and 11q and 17p (P<1 × 10−6). As we have identified that common variants of the LPHN3 gene were responsible for the 4q linkage signal, we focused on 4q–11q interaction to determine that single-nucleotide polymorphisms (SNPs) harbored in the LPHN3 gene interact with SNPs spanning the 11q region that contains DRD2 and NCAM1 genes, to double the risk of developing ADHD. This interaction not only explains genetic effects much better than taking each of these loci effects by separated but also differences in brain metabolism as depicted by proton magnetic resonance spectroscopy data and pharmacogenetic response to stimulant medication. These findings not only add information about how high order genetic interactions might be implicated in conferring susceptibility to develop ADHD but also show that future studies of the effects of genetic interactions on ADHD clinical information will help to shape predictive models of individual outcome
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