Development of Metamaterial EBG Absorbers for Application of Wireless Inter/Intrachip Communication Systems

First, the chapter presents a novel design of electromagnetic bandgap (EBG) absorber with the characteristics of broad bandwidth, low profile, and polarization‐independence to a normal incident electromagnetic wave. The absorber is composed of three consecutive octagon or decagon loops, and highly‐resistive frequency selective surface (FSS) layers. Second, based on the feature of the designed absorber unit, a broadband, metamaterial absorber‐bounded, wireless inter/intrachip (WIIC) communication channel is constructed at the center frequency of 60 GHz. Third, in order to validate the developed methodology used in WIIC analysis, a wired channel on a conventional PCB has been measured, simulated, and analyzed. Fourth, with the extracted S‐parameters of the WIIC system and wired PCB channel, the system impulse responses and transfer functions of the investigated channels have been further extracted, which are used for validation and BER analysis of the WIIC system. Finally, it has been shown that based on the derived BER results, the performance of the designed WIIC channel is close to that of an additive Gaussian white noise (AWGN) channel when the WIIC transceivers are built in with the functionalities of forward error control (FEC), channel estimation, and equalization

Environmental deterioration in rapid urbanisation: evidence from assessment of ecosystem service values in Wujiang, Suzhou

Land use change is the most prominent feature of Chinese urbanisation. In China, the expansion of land consumed for urban development is inevitable given the rapid increases in the urban economy and urban population, but also in meeting the population’s increasing demand for better quality of life. This paper is based on a research study of Wujiang district in Suzhou, which is considered representative of many of the rapid urbanisation areas within the nation. The objective is to develop an in-depth understanding of the characteristics of land use change and how this change contributes to environmental deterioration, as assessed by changes in the ecosystem service value (ESV). In this study, ESV is defined as the environmental products and functions provided for human well-being. Based on local planning documents, Landsat TM remote-sensing images and field surveys, the research analyses the cost to the environment when traditional land uses are transformed into urbanisation. The research demonstrates that conversion to urban land use which ignores the limit and capacity of the environment can generate significant environmental costs, as assessed by ESV, which in turn, can lead to a deterioration of quality of life for inhabitants, the exact opposite of the original intention. The research demonstrates that by mapping the spatial distribution of ecological service values, ESV can be used as a guide to urban sustainable development

ClickINC: In-network Computing as a Service in Heterogeneous Programmable Data-center Networks

In-Network Computing (INC) has found many applications for performance boosts or cost reduction. However, given heterogeneous devices, diverse applications, and multi-path network typologies, it is cumbersome and error-prone for application developers to effectively utilize the available network resources and gain predictable benefits without impeding normal network functions. Previous work is oriented to network operators more than application developers. We develop ClickINC to streamline the INC programming and deployment using a unified and automated workflow. ClickINC provides INC developers a modular programming abstractions, without concerning to the states of the devices and the network topology. We describe the ClickINC framework, model, language, workflow, and corresponding algorithms. Experiments on both an emulator and a prototype system demonstrate its feasibility and benefits

Molecular and clinical characteristics of ATP1A3-related diseases

ObjectiveWith detailed studies of ATP1A3-related diseases, the phenotypic spectrum of ATP1A3 has greatly expanded. This study aimed to potentially identify the mechanisms by which ATP1A3 caused neurological dysfunction by analyzing the clinical features and phenotypes of ATP1A3-related diseases, and exploring the distribution patterns of mutations in the subregions of the ATP1A3 protein, thus providing new and effective therapeutic approaches.MethodsDatabases of PubMed, Online Mendelian Inheritance in Man, and Human Gene Mutation Database, Wanfang Data, and Embase were searched for case reports of ATP1A3-related diseases. Following case screening, we collected clinical information and genetic testing results of patients, and analyzed the disease characteristics on the clinical phenotype spectrum associated with mutations, genetic characteristics of mutations, and effects of drug therapy.ResultsWe collected 902 clinical cases related to ATP1A3 gene. From the results of previous studies, we further clarified the clinical characteristics of ATP1A3-related diseases, such as alternating hemiplegia of childhood (AHC), rapid-onset dystonia-parkinsonism; cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss syndrome, and relapsing encephalopathy with cerebellar ataxia, frequency of mutations in different phenotypes and their distribution in gene and protein structures, and differences in mutations in different clinical phenotypes. Regarding the efficacy of drug treatment, 80 of the 124 patients with AHC were treated with flunarizine, with an effectiveness rate of ~64.5%.ConclusionsNervous system dysfunction due to mutations of ATP1A3 gene was characterized by a group of genotypic–phenotypic interrelated disease pedigrees with multiple clinical manifestations. The presented results might help guide the diagnosis and treatment of ATP1A3-related diseases and provided new ideas for further exploring the mechanisms of nervous system diseases due to ATP1A3 mutations

Identification of miRNAs and their target genes in developing maize ears by combined small RNA and degradome sequencing

Background In plants, microRNAs (miRNAs) are endogenous ~22 nt RNAs that play important regulatory roles in many aspects of plant biology, including metabolism, hormone response, epigenetic control of transposable elements, and stress response. Extensive studies of miRNAs have been performed in model plants such as rice and Arabidopsis thaliana. In maize, most miRNAs and their target genes were analyzed and identified by clearly different treatments, such as response to low nitrate, salt and drought stress. However, little is known about miRNAs involved in maize ear development. The objective of this study is to identify conserved and novel miRNAs and their target genes by combined small RNA and degradome sequencing at four inflorescence developmental stages. Results We used deep-sequencing, miRNA microarray assays and computational methods to identify, profile, and describe conserved and non-conserved miRNAs at four ear developmental stages, which resulted in identification of 22 conserved and 21-maize-specific miRNA families together with their corresponding miRNA*. Comparison of miRNA expression in these developmental stages revealed 18 differentially expressed miRNA families. Finally, a total of 141 genes (251 transcripts) targeted by 102 small RNAs including 98 miRNAs and 4 ta-siRNAs were identified by genomic-scale high-throughput sequencing of miRNA cleaved mRNAs. Moreover, the differentially expressed miRNAs-mediated pathways that regulate the development of ears were discussed. Conclusions This study confirmed 22 conserved miRNA families and discovered 26 novel miRNAs in maize. Moreover, we identified 141 target genes of known and new miRNAs and ta-siRNAs. Of these, 72 genes (117 transcripts) targeted by 62 differentially expressed miRNAs may attribute to the development of maize ears. Identification and characterization of these important classes of regulatory genes in maize may improve our understanding of molecular mechanisms controlling ear development

Genome-wide association study uncovers new genetic loci and candidate genes underlying seed chilling-germination in maize

As one of the major crops, maize (Zea mays L.) is mainly distributed in tropical and temperate regions. However, with the changes of the environments, chilling stress has become a significantly abiotic stress affecting seed germination and thus the reproductive and biomass accumulation of maize. Herein, we investigated five seed germination-related phenotypes among 300 inbred lines under low-temperature condition (10 °C). By combining 43,943 single nucleotide polymorphisms (SNPs), a total of 15 significant (P < 2.03 ×  10-6) SNPs were identified to correlate with seed germination under cold stress based on the FarmCPU model in GWAS, among which three loci were repeatedly associated with multiple traits. Ten gene models were closely linked to these three variations, among which Zm00001d010454, Zm00001d010458, Zm00001d010459, and Zm00001d050021 were further verified by candidate gene association study and expression pattern analysis. Importantly, these candidate genes were previously reported to involve plant tolerance to chilling stress and other abiotic stress. Our findings contribute to the understanding of the genetic and molecular mechanisms underlying chilling germination in maize

Genetic Polymorphisms in Enzymes Involved in One-Carbon Metabolism and Anti-epileptic Drug Monotherapy on Homocysteine Metabolism in Patients With Epilepsy

Aims: To investigate the effects of single nucleotide polymorphisms (SNPs) in genes of one-carbon metabolism (OCM) related enzymes and anti-epileptic drug (AED) monotherapy on homocysteine (Hcy) metabolism in patients with epilepsy, and to further explore specific SNPs that may increase patients' susceptibility to the effects of AEDs on the Hcy imbalance.Method: This case-control study analyzed 279 patients with epilepsy, including patients receiving monotherapy with valproate (VPA) (n = 53), oxcarbazepine (OXC) (n = 71), lamotrigine (LTG) (n = 55), or levetiracetam (LEV) (n = 35) and patients who had not taken any AEDs (controls, n = 65) for at least 6 months. Serum levels of vitamin B12 (vit B12), folate (FA) and Hcy were measured, and 23 SNPs in 13 genes of OCM-related enzymes were genotyped in all patients.Results: Methylenetetrahydrofolate reductase (MTHFR) rs1801133 was associated with elevated serum Hcy levels in patients with epilepsy (P &lt; 0.001), and patients presenting the TT genotype exhibited higher serum Hcy levels than patients with the CC (P &lt; 0.001) or CT (P &lt; 0.001) genotype. A subsequent multiple linear regression analysis showed that AED monotherapy with VPA (vs. control: P = 0.023) or OXC (vs. control: P = 0.041), and genotypes of MTHFR rs1801133 TT (vs. CC: P &lt; 0.001; vs. CT: P &lt; 0.001), transcobalamin 2 (TCN2) rs1801198 CC (vs. GC: P = 0.039) and folate receptor 1 (FOLR1) rs2071010 AA (vs. GA: P = 0.031) were independent risk factors for higher Hcy levels. In the subgroup analysis of patients taking OXC, we found that patients with genotypes of MTHFR rs1801133 TT (vs. CC: P = 0.001; vs. CT: P &lt; 0.001) and TCN2 rs1801198 CC (vs. GC: P = 0.021; vs. GG: P = 0.018) exhibited higher serum Hcy levels.Conclusions: VPA, OXC, and genotypes of MTHFR rs1801133 TT, TCN2 rs1801198 CC, and FOLR1 rs2071010 AA are all independent risk factors for elevated Hcy levels in patients with epilepsy. Moreover, genotypes of MTHFR rs1801133 TT and TCN2 rs1801198 CC may increase patients' susceptibility to the effect of OXC on disrupting Hcy homeostasis