Measuring the impact of adversarial errors on packet scheduling strategies

In this paper, we explore the problem of achieving efficient packet transmission over unreliable links with worst-case occurrence of errors. In such a setup, even an omniscient offline scheduling strategy cannot achieve stability of the packet queue, nor is it able to use up all the available bandwidth. Hence, an important first step is to identify an appropriate metric to measure the efficiency of scheduling strategies in such a setting. To this end, we propose an asymptotic throughput metric which corresponds to the long-term competitive ratio of the algorithm with respect to the optimal. We then explore the impact of the error detection mechanism and feedback delay on our measure. We compare instantaneous with deferred error feedback, which requires a faulty packet to be fully received in order to detect the error. We propose algorithms for worst-case adversarial and stochastic packet arrival models, and formally analyze their performance. The asymptotic throughput achieved by these algorithms is shown to be close to optimal by deriving lower bounds on the metric and almost matching upper bounds for any algorithm in the considered settings. Our collection of results demonstrate the potential of using instantaneous feedback to improve the performance of communication systems in adverse environments.     

Microfluidic chips for cells capture using 3-D hydrodynamic structure array

Microfluidic chips were designed and fabricated to capture cells in a relative small volume to generate the desired concentration needed for analysis. The microfluidic chips comprise three-dimensional (3-D) cell capture structures array fabricated in PDMS. The capture structure includes two layers. The first layer consists of spacers to create small gap between the upper layer and glass. The second layer is a sharp corner U-shaped compartment with sharp corners at the fore-end. And another type capture structure with Y-shaped fluidic guide has been designed. It was demonstrated that the structures can capture cells in theory, using Darcy–Weisbach equation and COMSOL Multiphysics. Then yeast cell was chosen to test the performance of the chips. The chip without fluid guides captured ~1.44 × 10⁵ cells and the capture efficiency was up to 71 %. And the chip with fluid guides captured ~5.0 × 10⁴ cells and the capture efficiency was ~25 %. The chip without fluid guides can capture more cells because the yeast cells in the chip without fluid guides are subject to larger hydrodynamic drag force.     

GI,biliary tract and pancreas

Percutaneous stent-grafting is increasingly employed as a less invasive alternative to surgery for the treatment of infrarenal abdominal aortic aneurysms. It requires long-term imaging follow-up, to document the structural integrity of the device, to exculude perigraft channels and endograft leakages, as well as the shrinkage of the aneurysmal sac. The expectation of severe stent induced artifacts and safety concerns have prevented 3D MRA from being used. The purpose of this in vitro study was to investigate the imaging characteristics of a bifurcated stent graft with 3D MRA (3D Frourier transform fast spoiled GRE) at 1.5 T in comparison to those of CTA. Measurement of the stent wall thickness and luminal diameter were made on a agar gel embedded stent graft at five locations on both CTA and MRA images. The stent graft was depicted as a dark ring on MR images. Wall thickness measurments at the five locations of the stent graft overestimated the true stent thickness, while luminal diameters were slightly underestimated. Measurement differences between MR and CT were not statistically significant (P=0.67;P=0.85). Artifacts emanating from the platinum markers were considerably less severe on the MR-images. A wider area of signal loss was seen only at the insertion of the iliac stent leg into the aortic stent portion due to the overlap of two radio-opaque platinum markers. 3D MRA images should permit a comprehensive assessment of the arterial lumen, and of perivascular tissues.     

颗粒物质控制膜污染的增强型膜生物反应器工艺的研究

用于废水处理的膜生物反应器工艺(MBR),是指通过膜过滤实现活性污泥与产水的分离的新型生化法处理废水技术.由于MBR具有占地面积小和出水水质好的优点,膜生物反应器成功应用到废水处理中的案例正在迅速增加.膜污染是MBR废水处理工艺面临的主要问题之一.膜污染会导致膜的渗透性能降低,为此必须通过化学清洗才能恢复膜的性能.为了实现无化学清洗的MBR工艺,研究使用持续物理冲刷去除膜污染层的方法.在活性污泥中加入颗粒物质(粉料),通过这些颗粒物质的持续冲刷作用实现去除膜污染层的目的.经过8个多月的实验,膜组件的渗透性能保持不变,通量可以达到40 L/(m2.h)以上.系统安装了在线的浊度仪作为产水质量的检测,在试验过程中,浊度始终没有变化.作为对比,同时也进行了一个参照实验(MBR标准工艺,没有加入颗粒物质),实验结果表明,传统的MBR工艺的膜组件渗透性能会不断下降导致通量下降,需要进行化学清洗.新型MBR工艺高通量和无需化学清洗的优势,将极大地提高MBR工艺的成本效益.     

Speciation and degradation of triphenyltin in typical paddy fields and its uptake into rice plants

Triphenyltin (TPhT) is a biocide used worldwide in agriculture, especially in rice crop farming. The distribution and dissipation of TPhT in rice fields, as well as uptake of TPhT and other phenyltin compounds (monophenyltin, MPhT, and diphenyltin, DPhT) is still unknown at present. In this study, speciation analysis of phenyltin compounds was carried out in soil and water from a rice field where TPhT was applied during rice seeding according to legal application rates in Brazil. The results indicate the degradation of biocide and distribution of tin species into soil and water. To evaluate whether TPhT is taken up by plants, rice plants were exposed to three different TPhT application rates in a controlled mesocosm during 7 weeks. After this period, tin speciation was determined in soil, roots, leaves, and grains of rice. Degradation of TPhT was observed in soil, where DPhT and MPhT were detected. MPhT, DPhT, and TPhT were also detected in the roots of plants exposed to all TPhT application rates. Only TPhT was detected in leaves and at relatively low concentration, suggesting selective transport of TPhT in the xylem, in contrast to DPhT and MPhT. Concentration of phenyltin species in rice grains was lower than the limit of detection, suggesting that rice plants do not have the capability to take up TPhT from soil and transport it to the grains.     

Physical aspects of cell culture substrates: topography, roughness, and elasticity

The cellular environment impacts a myriad of cellular functions by providing signals that can modulate cell phenotype and function. Physical cues such as topography, roughness, gradients, and elasticity are of particular importance. Thus, synthetic substrates can be potentially useful tools for exploring the influence of the aforementioned physical properties on cellular function. Many micro- and nanofabrication processes have been employed to control substrate characteristics in both 2D and 3D environments. This review highlights strategies for modulating the physical properties of surfaces, the influence of these changes on cell responses, and the promise and limitations of these surfaces in in-vitro settings. While both hard and soft materials are discussed, emphasis is placed on soft substrates. Moreover, methods for creating synthetic substrates for cell studies, substrate properties, and impact of substrate properties on cell behavior are the main focus of this review.