87 research outputs found
Research on active sound absorption based on minimality of quadratic sum of reflected sound pressure in low frequency
In this paper, the minimality of the quadratic sum of the reflected sound pressure is used to outline the method of active sound absorption. A piezoelectric ceramic is attached to a simply supported plate, and two microphones are placed in the front of the simply supported plate. The reflected sound pressure is measured. According to the measured reflected sound pressure, the voltage is added to the surface of the piezoelectric ceramic. Then, the simply supported plate is vibrated. Thus, the total sound pressure is expressed as a combination of the reflected sound pressure and the radiated sound pressure. A condition of the quadratic sum being minimal is presented and the voltage (added to the surface of the piezoelectric ceramic) is calculated. At last, the numerical calculation and the experiment are carried out, which demonstrate that the method outlined in this paper is possible
Observation of magnon-mediated current drag in Pt/yttrium iron garnet/Pt(Ta) trilayers
Pure spin current, a flow of spin angular momentum without flow of any
companying net charge, is generated in two common ways. One makes use of the
spin Hall effect in normal metals (NM) with strong spin-orbit coupling, such as
Pt or Ta. The other utilizes the collective motion of magnetic moments or spin
waves with the quasi-particle excitations called magnons. A popular material
for the latter is yttrium iron garnet, a magnetic insulator (MI). Here we
demonstrate in NM/MI/NM trilayers that these two types of spin currents are
interconvertible across the interfaces, predicated as the magnon-mediated
current drag phenomenon. The transmitted signal scales linearly with the
driving current without a threshold and follows the power-law with n ranging
from 1.5 to 2.5. Our results indicate that the NM/MI/NM trilayer structure can
serve as a scalable pure spin current valve device which is an essential
ingredient in spintronics
Preliminary study on early diagnosis of Alzheimer’s disease in APP/PS1 transgenic mice using multimodal magnetic resonance imaging
Alzheimer’s disease (AD) has an insidious onset and lacks clear early diagnostic markers, and by the time overt dementia symptoms appear, the disease is already in the mid-to-late stages. The search for early diagnostic markers of AD may open a critical window for Alzheimer’s treatment and facilitate early intervention to slow the progression of AD. In this study, we aimed to explore the imaging markers for early diagnosis of AD through the combined application of structural magnetic resonance imaging (sMRI), resting-state functional magnetic resonance imaging (rs-fMRI), and 1H-magnetic resonance spectroscopy (1H-MRS) multimodal magnetic resonance imaging (MRI) techniques at the animal experimental level, with the aim to provide a certain reference for early clinical diagnosis of AD. First, sMRI scans were performed on 4-month-old amyloid beta precursor protein/presenilin 1 (APP/PS1) transgenic AD model mice and wild type mice of the same litter using a 7.0 T animal MRI scanner to analyze the differential brain regions with structural changes in the gray matter of the brain by voxel-based morphometry (VBM). Next, rs-fMRI scans were performed to analyze the differential brain regions between groups for local spontaneous brain activity and functional connectivity (FC) between brain regions. Finally, 1H-MRS scans were performed to quantify and analyze intergroup differences in the relative concentrations of different metabolites within regions of interest (cortex and hippocampus). Compared with wild type mice, the volume of the left hippocampus, and right olfactory bulb of APP/PS1 transgenic AD model mice were reduced, the functional activity of the bilateral hippocampus, right piriform cortex and right caudate putamen was reduced, the functional network connectivity of the hippocampus was impaired, and the relative content of N-acetylaspartate (NAA)in the hippocampus was decreased. In addition, this study found that imaging changes in olfactory-related brain regions were closely associated with AD diagnosis, and these findings may provide some reference for the early diagnosis of AD
A large area, high counting rate micromegas-based neutron detector for BNCT
Beam monitoring and evaluation are very important to boron neutron capture
therapy (BNCT), and a variety of detectors have been developed for these
applications. However, most of the detectors used in BNCT only have a small
detection area, leading to the inconvenience of the full-scale 2-D measurement
of the beam. Based on micromegas technology, we designed a neutron detector
with large detection area and high counting rate. This detector has a detection
area of 288 mm multiples 288 mm and can measure thermal, epithermal, and fast
neutrons with different detector settings. The BNCT experiments demonstrated
that this detector has a very good 2-D imaging performance for the thermal,
epithermal, fast neutron and gamma components, a highest counting rate of 94
kHz/channel, and a good linearity response to the beam power. Additionally, the
flux fraction of each component can be calculated based on the measurement
results. The Am-Be neutron source experiment indicates that this detector has a
spatial resolution of approximately 1.4 mm, meeting the requirements of
applications in BNCT. It is evident that this micromegas-based neutron detector
with a large area and high counting rate capability has great development
prospects in BNCT beam monitoring and evaluation applications
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Limits of oxygen isotope palaeoaltimetry in Tibet
Measurements of stable water isotopes (oxygen and hydrogen) are commonly used to estimate palaeoelevation and quantify past changes in surface height across Tibet. Isotope palaeoaltimetry is often based on simple Rayleigh fractionation of a “parcel of air”, but must make a considerable number of approximations and assumptions. In this paper, we elaborate on the practicability of oxygen water isotopes in palaeoaltimetry, and evaluate a recent challenge to the palaeoaltimetry community. First, we examine the isotopic composition of oxygen (ẟ18O) versus altitude relationship in a set of five topographic realisations of Tibet using an isotope-enabled palaeoclimate model for the mid-Eocene, a period where a variety of topographic ‘uplift’ models have been proposed, and compare it to modern relationships. Second, we investigate whether isotopic composition is a good predictor of more modest changes in topography, such as the introduction of a valley system or uplift of only part of the Tibetan region. The aim of the paper is not to perform a direct comparison to data, but to use the model to further refine knowledge of the strengths and limitations of using oxygen isotopes in palaeoaltimetry. We find that oxygen isotope palaeoaltimetry works surprisingly well, with the exception that it could not identify low elevation valley systems bounded by high elevations because the isotopic composition of the water in the air becomes depleted at the first high elevation that an air parcel passes over and does not recover when it descends into the valley. Hence, isotope-based elevations are biased towards mountain range peaks. Overall, the application of oxygen isotope palaeoaltimetry does have value, but would be further strengthened when employed together with isotope-enabled models. In conjunction with other techniques such as terrestrial thermal lapse rates and energy conservation approaches, over a wide spatial region, a more accurate and fully three-dimension view of complex palaeo-topography is increasingly possible, which will in turn improve the precision of these palaeoaltimeters
Emilin1 gene and essential hypertension: a two-stage association study in northern Han Chinese population
<p>Abstract</p> <p>Background</p> <p>Elastogenesis of elastic extracellular matrix (ECM) which was recognized as a major component of blood vessels has been believed for a long time to play only a passive role in the dynamic vascular changes of typical hypertension. Emilin1 gene participated in the transcription of ECM's formation and was recognized to modulate links TGF-β maturation to blood pressure homeostasis in animal study. Recently relevant advances urge further researches to investigate the role of Emilin1 gene in regulating TGF-β signals involved in elastogenesis and vascular cell defects of essential hypertension (EH).</p> <p>Methods</p> <p>We designed a two-stage case-control study and selected three single nucleotide polymorphisms (SNPs), rs3754734, rs2011616 and rs2304682 from the HapMap database, which covered Emilin1 gene. Totally 2,586 subjects were recruited from the International Collaborative Study of Cardiovascular Disease in Asia (InterASIA). In stage 1, all the three SNPs of the Emilin1 gene were genotyped and tested within a subsample including 503 cases and 490 controls, significant SNPs would enter into stage 2 including 814 cases with hypertension and 779 controls and analyze on the basis of testing total 2,586 subjects.</p> <p>Results</p> <p>In stage 1, single locus analyses showed that SNPs rs3754734 and rs2011616 had significant association with EH (P < 0.05). In stage 2, weak association for dominant model were observed by age stratification and odds ratio (ORs) of TG+GG vs. TT of rs3754734 were 0.768 (0.584-1.009), 0.985 (0.735-1.320) and 1.346 (1.003-1.806) in < 50, 50-59 and ≥ 60 years group and ORs of GA+AA vs. GG of rs2011616 were 0.745 (0.568-0.977), 1.013 (0.758-1.353) and 1.437 (1.072-1.926) in < 50, 50-59 and ≥ 60 years group respectively. Accordingly, significant interactions were detected between genotypes of rs3754734 and rs2011616 and age for EH, and ORs were 1.758 (1.180-2.620), P = 0.006 and 1.903 (1.281-2.825), P = 0.001, respectively. Results of haplotypes analysis showed that there weren't any haplotypes associated with EH directly, but the interaction of hap2 (GA) and age-group found to be significant after being adjusted for the covariates, OR was 1.220 (1.031-1.444), P value was 0.020.</p> <p>Conclusion</p> <p>Our findings don't support positive association of Emilin1 gene with EH, but the interaction of age and genotype variation of rs3754734 and rs2011616 might increase the risk to hypertension.</p
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
Reduced glomerular filtration rate defines chronic kidney disease and is associated with cardiovascular and all-cause mortality. We conducted a meta-analysis of genome-wide association studies for estimated glomerular filtration rate (eGFR), combining data across 133,413 individuals with replication in up to 42,166 individuals. We identify 24 new and confirm 29 previously identified loci. Of these 53 loci, 19 associate with eGFR among individuals with diabetes. Using bioinformatics, we show that identified genes at eGFR loci are enriched for expression in kidney tissues and in pathways relevant for kidney development and transmembrane transporter activity, kidney structure, and regulation of glucose metabolism. Chromatin state mapping and DNase I hypersensitivity analyses across adult tissues demonstrate preferential mapping of associated variants to regulatory regions in kidney but not extra-renal tissues. These findings suggest that genetic determinants of eGFR are mediated largely through direct effects within the kidney and highlight important cell types and biological pathways
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