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.
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.
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.
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