When Does Relay Transmission Give a More Secure Connection in Wireless Ad Hoc Networks?

Relay transmission can enhance coverage and throughput, while it can be vulnerable to eavesdropping attacks due to the additional transmission of the source message at the relay. Thus, whether or not one should use relay transmission for secure communication is an interesting and important problem. In this paper, we consider the transmission of a confidential message from a source to a destination in a decentralized wireless network in the presence of randomly distributed eavesdroppers. The source-destination pair can be potentially assisted by randomly distributed relays. For an arbitrary relay, we derive exact expressions of secure connection probability for both colluding and non-colluding eavesdroppers. We further obtain lower bound expressions on the secure connection probability, which are accurate when the eavesdropper density is small. By utilizing these lower bound expressions, we propose a relay selection strategy to improve the secure connection probability. By analytically comparing the secure connection probability for direct transmission and relay transmission, we address the important problem of whether or not to relay and discuss the condition for relay transmission in terms of the relay density and source-destination distance. These analytical results are accurate in the small eavesdropper density regime.Comment: Accepted for publication in IEEE Transactions On Information Forensics and Securit

And They Saved My Sorry Ass: A Documentary Discovering Self in Contemporary Fan Culture

And They Saved My Sorry Ass is a documentary/personal essay film about queer ani- me lovers (including the filmmaker) based both in the US and in China. This film focuses on how these fans express their identities by embodying and re-interpreting anime characters. Experimental methods, such as staged performance, first-person narration and abstract imaging are explored in addition to conventional interviews. This thesis follows the pre-production, production and post-production processes of making this film through 2020 to 2023, also mapping out marketing and distribution plans after finishing the project

Temperature and Development Impacts on Housekeeping Gene Expression in Cowpea Aphid, \u3cem\u3eAphis craccivora\u3c/em\u3e (Hemiptera: Aphidiae)

Quantitative real-time PCR (qRT-PCR) is a powerful technique to quantify gene expression. To standardize gene expression studies and obtain more accurate qRT-PCR analysis, normalization relative to consistently expressed housekeeping genes (HKGs) is required. In this study, ten candidate HKGs including elongation factor 1 α (EF1A), ribosomal protein L11 (RPL11), ribosomal protein L14 (RPL14), ribosomal protein S8 (RPS8), ribosomal protein S23 (RPS23), NADH-ubiquinone oxidoreductase (NADH), vacuolar-type H+-ATPase (ATPase), heat shock protein 70 (HSP70), 18S ribosomal RNA (18S), and 12S ribosomal RNA (12S) from the cowpea aphid, Aphis craccivora Koch were selected. Four algorithms, geNorm, Normfinder, BestKeeper, and the ΔCt method were employed to evaluate the expression profiles of these HKGs as endogenous controls across different developmental stages and temperature regimes. Based on RefFinder, which integrates all four analytical algorithms to compare and rank the candidate HKGs, RPS8, RPL14, and RPL11 were the three most stable HKGs across different developmental stages and temperature conditions. This study is the first step to establish a standardized qRT-PCR analysis in A. craccivora following the MIQE guideline. Results from this study lay a foundation for the genomics and functional genomics research in this sap-sucking insect pest with substantial economic impact

Digital Technology-driven Business Model Innovations: A Bibliometric Analysis

With the advent of the data age, digital technology has been widely used in business model innovation. To understand the current research situation in the field of digital technology-driven business model innovation and reveal the knowledge structure, research hotspots, and development trends in this research field, this paper adopts statistical analysis, co-citation analysis, cluster analysis and other methods to carry out bibliometric analysis and knowledge mapping on the relevant literature included in the Web of Science database. The research results show that customer relationship management, digital economy and financial service system, sustainable development and digital service innovation, and the competition and cooperation mechanism of enterprises are hot topics in this field. Moreover, digital platform, firm performance, and value creation are the main research directions in the future

Stably Expressed Housekeeping Genes across Developmental Stages in the Two-Spotted Spider Mite, \u3cem\u3eTetranychus urticae\u3c/em\u3e

Quantitative real-time PCR (qRT-PCR) is a reliable and reproducible technique for measuring mRNA expression. To facilitate gene expression studies and obtain more accurate qRT-PCR analysis, normalization relative to stable housekeeping genes is mandatory. In this study, ten housekeeping genes, including beta-actin (Actin), elongation factor 1 α (EF1A), glyceralde hyde-3-phosphate dehydrogenase (GAPDH), ribosomal protein L13 (RPL13), ribosomal protein 49 (RP49), α-tubulin (Tubulin), vacuolar-type H+-ATPase (v-ATPase), succinate dehydrogenase subunit A (SDHA) , 28S ribosomal RNA (28S), and 18S ribosomal RNA (18S) from the two-spotted spider mite, Tetranychus urticae, were selected as the candidate reference genes. Four algorithms, geNorm, Normfinder, BestKeeper, and the ΔCt method, were used to evaluate the performance of these candidates as endogenous controls across different developmental stages. In addition, RefFinder, which integrates the above-mentioned software tools, provided the overall ranking of the stability/suitability of these candidate reference genes. Among them, PRL13 and v-ATPase were the two most stable housekeeping genes across different developmental stages. This work is the first step toward establishing a standardized qRT-PCR analysis in T. urticae following the MIQE guideline. With the recent release of the T. urticae genome, results from this study provide a critical piece for the subsequent genomics and functional genomics research in this emerging model system

Selection of Reference Genes for Expression Analysis Using Quantitative Real-Time PCR in the Pea Aphid, \u3cem\u3eAcyrthosiphon pisum\u3c/em\u3e (Harris) (Hemiptera, Aphidiae)

To facilitate gene expression study and obtain accurate qRT-PCR analysis, normalization relative to stable expressed housekeeping genes is required. In this study, expression profiles of 11 candidate reference genes, including actin (Actin), elongation factor 1 α (EF1A), TATA-box-binding protein (TATA), ribosomal protein L12 (RPL12), β-tubulin (Tubulin), NADH dehydrogenase (NADH), vacuolar-type H+-ATPase (v-ATPase), succinate dehydrogenase B (SDHB), 28S ribosomal RNA (28S), 16S ribosomal RNA (16S), and 18S ribosomal RNA (18S) from the pea aphid Acyrthosiphon pisum, under different developmental stages and temperature conditions, were investigated. A total of four analytical tools, geNorm, Normfinder, BestKeeper, and the ΔCt method, were used to evaluate the suitability of these genes as endogenous controls. According to RefFinder, a web-based software tool which integrates all four above-mentioned algorithms to compare and rank the reference genes, SDHB, 16S, and NADH were the three most stable house-keeping genes under different developmental stages and temperatures. This work is intended to establish a standardized qRT-PCR protocol in pea aphid and serves as a starting point for the genomics and functional genomics research in this emerging insect model