393 research outputs found
Frequency modulated self-oscillation and phase inertia in a synchronized nanowire mechanical resonator
Synchronization has been reported for a wide range of self-oscillating
systems. However, even though it has been predicted theoretically for several
decades, the experimental realization of phase self-oscillation, sometimes
called phase trapping, in the high driving regime has been studied only
recently. We explored in detail the phase dynamics in a synchronized field
emission SiC nanoelectromechanical system with intrinsic feedback. A richer
variety of phase behavior has been unambiguously identified, implying phase
modulation and inertia. This synchronization regime is expected to have
implications for the comprehension of the dynamics of interacting
self-oscillating networks and for the generation of frequency modulated signals
at the nanoscal
Role of fluctuations and nonlinearities on field emission nanomechanical self-oscillators
A theoretical and experimental description of the threshold, amplitude, and
stability of a self-oscillating nanowire in a field emission configuration is
presented. Two thresholds for the onset of self-oscillation are identified, one
induced by fluctuations of the electromagnetic environment and a second
revealed by these fluctuations by measuring the probability density function of
the current. The ac and dc components of the current and the phase stability
are quantified. An ac to dc ratio above 100% and an Allan deviation of 1.3x10-5
at room temperature can be attained. Finally, it is shown that a simple
nonlinear model cannot describe the equilibrium effective potential in the
self-oscillating regime due to the high amplitude of oscillations
Current Saturation in Field Emission from H-Passivated Si Nanowires
International audienceThis paper explores the field emission (FE) properties of highly crystalline Si nanowires (NWs) with controlled surface passivation. The NWs were batch-grown by the vapor_liquid_solid process using Au catalysts with no intentional doping. The FE current_voltage characteristics showed quasi-ideal current saturation that resembles those predicted by the basic theory for emission from semiconductors, even at room temperature. In the saturation region, the currents were extremely sensitive to temperature and also increased linearly with voltage drop along the nanowire. The latter permits the estimation of the doping concentration and the carrier lifetime, which is limited by surface recombination. The conductivity could be tuned over 2 orders of magnitude by in situ hydrogen passivation/desorption cycles. This work highlights the role of dangling bonds in surface leakage currents and demonstrates the use of hydrogen passivation for optimizing the FE characteristics of Si NWs
High Frequency top-down Junction-less Silicon Nanowire Resonators
We report here the first realization of top-down silicon nanowires (SiNW)
transduced by both junction-less field effect transistor (FET) and the
piezoresistive (PZR) effect. The suspended SiNWs are among the smallest
top-down SiNWs reported to date, featuring widths down to ~20nm. This has been
achieved thanks to a 200mm-wafer-scale, VLSI process fully amenable to
monolithic CMOS co-integration. Thanks to the very small dimensions, the
conductance of the silicon nanowire can be controlled by a nearby electrostatic
gate. Both the junction-less FET and the previously demonstrated PZR
transduction have been performed with the same SiNW. These self-transducing
schemes have shown similar signal-to-background ratios, and the PZR
transduction has exhibited a relatively higher output signal. Allan deviation
AD of the same SiNW has been measured with both schemes, and we obtain AD~20ppm
for the FET detection and AD~3ppm for the PZR detection at room temperature and
low pressure. Orders of magnitude improvements are expected from tighter
electrostatic control via changes in geometry and doping level, as well as from
CMOS integration. The compact, simple topology of these elementary SiNW
resonators opens up new paths towards ultra-dense arrays for gas and mass
sensing, time keeping or logic switching systems in SiNW-CMOS platform
Nonlinear polarization coupling in freestanding nanowire/nanotube resonators
In this work, we study the nonlinear coupling between the transverse modes of nanoresonators such as nanotubes or nanowires in a singly clamped configuration. We previously showed that at high driving, this coupling could result in a transition from independent planar modes to a locked elliptical motion, with important modifications of the resonance curves. Here, we clarify the physical origins, associated with a 1:1 internal resonance, and study in depth this transition as a function of the relevant parameters. We present simple formulae that permit to predict the emergence of this transition as a function of the frequency difference between the polarizations and the nonlinear coefficients and give the “backbone curves” corresponding to the elliptical regime. We also show that the elliptical regime is associated with the emergence of a new set of solutions of which one branch is stable. Finally, we compare single and double clamped configurations and explain why the elliptical transition appears on different polarizations
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Miles to go (mtgo) encodes FNDC3 proteins that interact with the chaperonin subunit CCT3 and are required for NMJ branching and growth in Drosophila.
Analysis of mutants that affect formation and function of the Drosophila larval neuromuscular junction (NMJ) has provided valuable insight into genes required for neuronal branching and synaptic growth. We report that NMJ development in Drosophila requires both the Drosophila ortholog of FNDC3 genes; CG42389 (herein referred to as miles to go; mtgo), and CCT3, which encodes a chaperonin complex subunit. Loss of mtgo function causes late pupal lethality with most animals unable to escape the pupal case, while rare escapers exhibit an ataxic gait and reduced lifespan. NMJs in mtgo mutant larvae have dramatically reduced branching and growth and fewer synaptic boutons compared with control animals. Mutant larvae show normal locomotion but display an abnormal self-righting response and chemosensory deficits that suggest additional functions of mtgo within the nervous system. The pharate lethality in mtgo mutants can be rescued by both low-level pan- and neuronal-, but not muscle-specific expression of a mtgo transgene, supporting a neuronal-intrinsic requirement for mtgo in NMJ development. Mtgo encodes three similar proteins whose domain structure is most closely related to the vertebrate intracellular cytosolic membrane-anchored fibronectin type-III domain-containing protein 3 (FNDC3) protein family. Mtgo physically and genetically interacts with Drosophila CCT3, which encodes a subunit of the TRiC/CCT chaperonin complex required for maturation of actin, tubulin and other substrates. Drosophila larvae heterozygous for a mutation in CCT3 that reduces binding between CCT3 and MTGO also show abnormal NMJ development similar to that observed in mtgo null mutants. Hence, the intracellular FNDC3-ortholog MTGO and CCT3 can form a macromolecular complex, and are both required for NMJ development in Drosophila
Resolving the ancestry of Austronesian-speaking populations
There are two very different interpretations of the prehistory of Island Southeast Asia (ISEA), with genetic evidence invoked in support of both. The “out-of-Taiwan” model proposes a major Late Holocene expansion of Neolithic Austronesian speakers from Taiwan. An alternative, proposing that Late Glacial/postglacial sea-level rises triggered largely autochthonous dispersals, accounts for some otherwise enigmatic genetic patterns, but fails to explain the Austronesian language dispersal. Combining mitochondrial DNA (mtDNA), Y-chromosome and genome-wide data, we performed the most comprehensive analysis of the region to date, obtaining highly consistent results across all three systems and allowing us to reconcile the models. We infer a primarily common ancestry for Taiwan/ISEA populations established before the Neolithic, but also detected clear signals of two minor Late Holocene migrations, probably representing Neolithic input from both Mainland Southeast Asia and South China, via Taiwan. This latter may therefore have mediated the Austronesian language dispersal, implying small-scale migration and language shift rather than large-scale expansion
Genome-wide analysis of ivermectin response by Onchocerca volvulus reveals that genetic drift and soft selective sweeps contribute to loss of drug sensitivity
Treatment of onchocerciasis using mass ivermectin administration has reduced morbidity and transmission throughout Africa and Central/South America. Mass drug administration is likely to exert selection pressure on parasites, and phenotypic and genetic changes in several Onchocerca volvulus populations from Cameroon and Ghana-exposed to more than a decade of regular ivermectin treatment-have raised concern that sub-optimal responses to ivermectin's anti-fecundity effect are becoming more frequent and may spread.Pooled next generation sequencing (Pool-seq) was used to characterise genetic diversity within and between 108 adult female worms differing in ivermectin treatment history and response. Genome-wide analyses revealed genetic variation that significantly differentiated good responder (GR) and sub-optimal responder (SOR) parasites. These variants were not randomly distributed but clustered in ~31 quantitative trait loci (QTLs), with little overlap in putative QTL position and gene content between the two countries. Published candidate ivermectin SOR genes were largely absent in these regions; QTLs differentiating GR and SOR worms were enriched for genes in molecular pathways associated with neurotransmission, development, and stress responses. Finally, single worm genotyping demonstrated that geographic isolation and genetic change over time (in the presence of drug exposure) had a significantly greater role in shaping genetic diversity than the evolution of SOR.This study is one of the first genome-wide association analyses in a parasitic nematode, and provides insight into the genomics of ivermectin response and population structure of O. volvulus. We argue that ivermectin response is a polygenically-determined quantitative trait (QT) whereby identical or related molecular pathways but not necessarily individual genes are likely to determine the extent of ivermectin response in different parasite populations. Furthermore, we propose that genetic drift rather than genetic selection of SOR is the underlying driver of population differentiation, which has significant implications for the emergence and potential spread of SOR within and between these parasite populations
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Most common human traits and diseases have a polygenic pattern of inheritance: DNA sequence variants at many genetic loci influence the phenotype. Genome-wide association (GWA) studies have identified more than 600 variants associated with human traits, but these typically explain small fractions of phenotypic variation, raising questions about the use of further studies. Here, using 183,727 individuals, we show that hundreds of genetic variants, in at least 180 loci, influence adult height, a highly heritable and classic polygenic trait. The large number of loci reveals patterns with important implications for genetic studies of common human diseases and traits. First, the 180 loci are not random, but instead are enriched for genes that are connected in biological pathways (P = 0.016) and that underlie skeletal growth defects (P < 0.001). Second, the likely causal gene is often located near the most strongly associated variant: in 13 of 21 loci containing a known skeletal growth gene, that gene was closest to the associated variant. Third, at least 19 loci have multiple independently associated variants, suggesting that allelic heterogeneity is a frequent feature of polygenic traits, that comprehensive explorations of already-discovered loci should discover additional variants and that an appreciable fraction of associated loci may have been identified. Fourth, associated variants are enriched for likely functional effects on genes, being over-represented among variants that alter amino-acid structure of proteins and expression levels of nearby genes. Our data explain approximately 10% of the phenotypic variation in height, and we estimate that unidentified common variants of similar effect sizes would increase this figure to approximately 16% of phenotypic variation (approximately 20% of heritable variation). Although additional approaches are needed to dissect the genetic architecture of polygenic human traits fully, our findings indicate that GWA studies can identify large numbers of loci that implicate biologically relevant genes and pathways.
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