Dynamic feature analysis of handwritten electronic signatures based on Fourier transform.

The utilization of handwritten electronic signatures has expanded in various application scenarios, leading to an increased demand for identification. Unlike handwriting signatures, handwritten electronic signatures offer the advantage of extracting dynamic feature data, including writing pressure, velocity, and acceleration. In this study, the Fourier transform was employed to extract 18 characteristics from the time domain and frequency domain of writing pressure, velocity, and acceleration. The experimental findings revealed distinguishable differences between genuine signatures and random forgeries in writing pressure. However, no statistically significant differences were observed in writing velocity and writing acceleration. Moreover, significant differences were detected in most characteristics when comparing genuine signatures with freehand imitation forgeries and tracing imitation forgeries. The canonical discriminant analysis was performed between the genuine and Non-genuine signatures; the cross-validation estimated the discriminating power of these characteristics with a satisfactory result. The study proposed a new approach to analyzing handwritten electronic signatures using time-domain and frequency-domain characteristics and demonstrated its effectiveness in the examination.

A cotton endoreduplication gene, GaTOP6B, regulates trichome branching development.

Trichomes are specialized epidermal structures that protect plants from biotic and abiotic stresses by synthesizing, storing, and secreting defensive compounds. This study investigates the role of the Gossypium arboreum DNA topoisomerase VI subunit B gene (GaTOP6B) in trichome development and branching. Sequence alignment revealed a high similarity between GaTOP6B and AtTOP6B, suggesting a conserved function in trichome regulation. Although AtTOP6B acts as a positive regulator of trichome development, functional analyses showed contrasting effects: Virus-induced gene silencing (VIGS) of GaTOP6B in cotton increased trichome density, while its overexpression in Arabidopsis decreased trichome density but enhanced branching. This demonstrates that GaTOP6B negatively regulates trichome number, indicating species-specific roles in trichome initiation and branching between cotton and Arabidopsis. Overexpression of the GaTOP6B promotes jasmonic acid synthesis, which in turn inhibits the G1/S or G2/M transitions, stalling the cell cycle. On the other hand, it suppresses brassinolide synthesis and signaling while promoting cytokinin degradation, further inhibiting mitosis. These hormonal interactions facilitate the transition of cells from the mitotic cycle to the endoreduplication cycle. As the level of endoreduplication increases, trichomes develop an increased number of branches. These findings highlight GaTOP6B's critical role as a regulator of trichome development, providing new genetic targets for improving cotton varieties in terms of enhanced adaptability and resilience.

Transcriptome Profiling Identifies Candidate Genes Contributing to Male and Female Gamete Development in Synthetic Brassica Allohexaploids.

Polyploidy plays a crucial role in plant evolution and speciation. The development of male and female gametes is essential to the reproductive capacity of polyploids, but their gene expression pattern has not been fully explored in newly established polyploids. The present study aimed to reveal a detailed atlas of gene expression for gamete development in newly synthetic Brassica allohexaploids that are not naturally existing species. Comparative transcriptome profiling between developing anthers (staged from meiosis to mature pollen) and ovules (staged from meiosis to mature embryo sac) was performed using RNA-Seq analysis. A total of 8676, 9775 and 4553 upregulated differentially expressed genes (DEGs) were identified for the development of both gametes, for male-only, and for female-only gamete development, respectively, in the synthetic Brassica allohexaploids. By combining gene ontology (GO) biological process analysis and data from the published literature, we identified 37 candidate genes for DNA double-strand break formation, synapsis and the crossover of homologous recombination during male and female meiosis and 51 candidate genes for tapetum development, sporopollenin biosynthesis and pollen wall development in male gamete development. Furthermore, 23 candidate genes for mitotic progression, nuclear positioning and cell specification and development were enriched in female gamete development. This study lays a good foundation for revealing the molecular regulation of genes related to male and female gamete development in Brassica allohexaploids and provides more resourceful genetic information on the reproductive biology of Brassica polyploid breeding.

Stability and Specificity of Counterfeit Protection System Code.

In this study, the stability and specificity of a counterfeit protection system (CPS) code were determined. This research involved an analysis of a counterfeit protection system code unit over time using the pattern location measurement method. We collected 379 sample sheets from 196 printers or photocopiers, covering 14 original brands, including 129 models. There was an interval of at least two months between the collections of samples from each machine. Four types of characteristics were established: CPS pattern unit, distance of the CPS unit, position of dots, size and shape of the dot. Except for the partial changes in the Xerox brand, no other brand exhibited changes over time. This implies that the CPS characteristics are stable. Meanwhile, no correlation was noted between the combinations of the characteristic systems in the collected samples, which implied strong specificity.

Study of Color Laser Printer and Photocopier Class Using a Pattern Location Measurement Method.

A trace code pattern location measurement approach is proposed. It includes a method that can precisely extract the trace code pattern to identify the color laser printer or photocopier class. In this study, we collected 379 samples from 15 brands, including 129 models and 196 printers or photocopiers. The trace code pattern class is identified. Four class characteristics are used to identify the print source: (i) the relation between the pattern and print output direction; (ii) observation of the shape features from among the trace code pattern units; (iii) the feature arrangement from among the trace code pattern units; and (iv) the arrangement relation of the trace code pattern. Blind testing shows that the accuracy of the proposed method is approximately 96.9% for the Questioned Document Examiners, and 84.3% in the non-Questioned Document Examiners. It is thus an effective technique for determining a print's color laser printer or photocopier source class.