The Secret to Popular Chinese Web Novels: A Corpus-Driven Study

What is the secret to writing popular novels? The issue is an intriguing one among researchers from various fields. The goal of this study is to identify the linguistic features of several popular web novels as well as how the textual features found within and the overall tone interact with the genre and themes of each novel. Apart from writing style, non-textual information may also reveal details behind the success of web novels. Since web fiction has become a major industry with top writers making millions of dollars and their stories adapted into published books, determining essential elements of "publishable" novels is of importance. The present study further examines how non-textual information, namely, the number of hits, shares, favorites, and comments, may contribute to several features of the most popular published and unpublished web novels. Findings reveal that keywords, function words, and lexical diversity of a novel are highly related to its genres and writing style while dialogue proportion shows the narration voice of the story. In addition, relatively shorter sentences are found in these novels. The data also reveal that the number of favorites and comments serve as significant predictors for the number of shares and hits of unpublished web novels, respectively; however, the number of hits and shares of published web novels is more unpredictable

A Mobile Learning Support System for Ubiquitous Learning Environments

AbstractThis paper proposes a Mobile Learning Support System (MLSS) which enables students to access learning materials by utilizing 2D barcodes and GPS technology. As the pilot system of ubiquitous learning, we used camera-equipped mobile phones and 2D barcode tags to obtain learning information from online websites. By installing the MLSS on to their mobile phones, students can scan the tag attached to the corresponding object to display related multimedia materials on the screen of mobile phones. Furthermore, MLSS also applies GPS technology to develop a location-aware environment for students. GPS technology is used to detect the students’ location and identify which 2D barcode tags are in their proximity. Therefore, this paper provides the opportunity to develop for developers create ubiquitous learning environments that combine real-world and digital world resources

Performance of Joint Channel and Physical Network Coding Based on Alamouti STBC

This work considers the protograph-coded physical network coding (PNC) based on Alamouti space-time block coding (STBC) over Nakagami-fading two-way relay channels, in which both the two sources and relay possess two antennas. We first propose a novel precoding scheme at the two sources so as to implement the iterative decoder efficiently at the relay. We further address a simplified updating rule of the log-likelihood-ratio (LLR) in such a decoder. Based on the simplified LLR-updating rule and Gaussian approximation, we analyze the theoretical bit-error-rate (BER) of the system, which is shown to be consistent with the decoding thresholds and simulated results. Moreover, the theoretical analysis has lower computational complexity than the protograph extrinsic information transfer (PEXIT) algorithm. Consequently, the analysis not only provides a simple way to evaluate the error performance but also facilitates the design of the joint channel-and-PNC (JCNC) in wireless communication scenarios.Comment: 6 pages, 4 figures, accpete

The Hop-Like Stress-Induced Protein 1 Cochaperone is a Novel Cell-Intrinsic Restriction Factor for Mitochondrial Tombusvirus Replication

Recent genome-wide screens reveal that the host cells express an arsenal of proteins that inhibit replication of plus-stranded RNA viruses by functioning as cell-intrinsic restriction factors of viral infections. One group of cell-intrinsic restriction factors against tombusviruses contains tetratricopeptide repeat (TPR) domains that directly interact with the viral replication proteins. In this paper, we find that the TPR domain-containing Hop-like stress-inducible protein 1 (Sti1p) cochaperone selectively inhibits the mitochondrial membrane-based replication of Carnation Italian ringspot tombusvirus (CIRV). In contrast, Sti1/Hop does not inhibit the peroxisome membrane-based replication of the closely related Tomato bushy stunt virus (TBSV) or Cucumber necrosis virus (CNV) in a yeast model or in plants. Deletion of STI1 in yeast leads to up to a 4-fold increase in CIRV replication, and knockdown of the orthologous Hop cochaperone in plants results in a 3-fold increase in CIRV accumulation. Overexpression of Sti1p derivatives in yeast reveals that the inhibitory function depends on the TPR1 domain known to interact with heat shock protein 70 (Hsp70), but not on the TPR2 domain interacting with Hsp90. In vitro CIRV replication studies based on isolated mitochondrial preparations and purified recombinant proteins has confirmed that Sti1p, similar to the TPR-containing Cyp40-like Cpr7p cyclophilin and the Ttc4 oncogene-like Cns1 cochaperone, is a strong inhibitor of CIRV replication. Sti1p interacts and colocalizes with the CIRV replication proteins in yeast. Our findings indicate that the TPR-containing Hop/Sti1 cochaperone could act as a cell-intrinsic virus restriction factor of the mitochondrial CIRV, but not against the peroxisomal tombusviruses in yeast and plants. IMPORTANCE: The host cells express various cell-intrinsic restriction factors that inhibit the replication of plus-stranded RNA viruses. In this paper, the authors find that the Hop-like stress-inducible protein 1 (Sti1p) cochaperone selectively inhibits the mitochondrial membrane-based replication of Carnation Italian ringspot tombusvirus (CIRV) in yeast. Deletion of STI1 in yeast or knockdown of the orthologous Hop cochaperone in plants leads to increased CIRV replication. In addition, overexpression of Sti1p derivatives in yeast reveals that the inhibitory function depends on the TPR1 domain known to interact with heat shock protein 70 (Hsp70), but not on the TPR2 domain interacting with Hsp90. In vitro CIRV replication studies based on isolated mitochondrial preparations and purified recombinant proteins have confirmed that Sti1p is a strong inhibitor of CIRV replication. The authors\u27 findings reveal that the Hop/Sti1 cochaperone could act as a cell-intrinsic restriction factor against the mitochondrial CIRV, but not against the related peroxisomal tombusviruses