• Title/Summary/Keyword: Amphioctopus fangsiao

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Spawning Period and Estimated Recreational Catch of Amphioctopus fangsiao in the Coastal Waters of Jeollanam-do, Korea (전라남도 연안에 서식하는 주꾸미(Amphioctopus fangsiao)의 산란시기와 유어낚시 어획실태)

  • Moon, Seong Yong;Kim, Heeyong;Lee, Mi Hee;Jung, Kyung Mi;Kim, Maeng Jin
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.55 no.1
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    • pp.61-66
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    • 2022
  • Amphioctopus fangsiao is a crucial fishery stock located off Korea's western and southern coasts. In this study, we present data on the spawning period and estimated recreational catch of A. fangsiao in the coastal waters of Jeollanam-do, South Korea. The overall sex ratio was estimated to be 1:1.13 (female: male); in females and males, the gonadosomatic index ranged from 1.22 to 12.14 and 0.17 to 3.44, respectively. The breeding season lasted from December to May, with spawning peaks observed between March and May. Furthermore, the estimated total annual recreational catch of A. fangsiao was 185,085 kg, with November recording the highest recreational catch. A. fangsiao catch per unit effort (CPUE) ranged from 3 to 302.4 kg per vessel d-1. Therefore, these findings underscore the need for additional monitoring, as any further assessment of A. fangsiao stock necessitates an understanding of recreational catch assessment and fishing efforts in Jeollanam- do's coastal waters.

Monitoring of Commercial Products Sold on Sushi Buffet Restaurants in South Korea using DNA Barcode Information (국내 대형 초밥 뷔페에서 사용되는 수산물의 원재료 모니터링 연구)

  • Kang, Tae Sun
    • Journal of Food Hygiene and Safety
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    • v.35 no.1
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    • pp.45-50
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    • 2020
  • In this study, seafood products (n=26) sold on sushi buffet restaurants in the city of Wonju were monitored by analyzing sequences of DNA barcode markers (cytochrome c oxidase subunit I and 16S ribosomal RNA genes). NCBI BLAST database was screened with the barcode sequences analyzed as a query for species identification. The BLAST search revealed that fifteen samples (58%) analyzed were consistent with their labeling information; however, the ingredients used in seven samples (27%) were not compliant with their label information. In the case of these mislabeled products, ingredients for sutchi catfish sushi and cherry bass sashimi were identified as Pangasianodon hypophthalmus and Lampris guttatus, respectively. For Japanese flying-fish roe sushi and Pacific herring roe sushi, roe of Mallotus villosus was used as an ingredient. Amphioctopus fangsiao and A. membranaceus were used in octopus sushi and soybean-marinated squid products, respectively. This monitoring result can contribute to the protection of consumer rights and the reduction of fraudulent practices in the food industry.

Development and Validation of Quick and Accurate Cephalopods Grouping System in Fishery Products by Real-time Quantitative PCR Based on Mitochondrial DNA (두족류의 진위 판별을 위한 Real-time Quantitative PCR 검사법 개발 및 검증)

  • Chung, In Young;Seo, Yong Bae;Yang, Ji Young;Kwon, Ki sung;Kim, Gun Do
    • Journal of Food Hygiene and Safety
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    • v.33 no.4
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    • pp.280-288
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    • 2018
  • In this study, an approach for the analysis of the five cephalopod species (octopus, long-arm octopus, squid, wet-foot octopus, beka squid) consumed in the Republic of Korea is developed. The samples were collected from the Southeast Asian countries Thailand, Indonesia, Vietnam, and China. The SYBR-green-based real-time qPCR method, based on the mitochondrial DNA genome of the five cephalopods was developed and validated. The intergroup variations in the mitochondrial DNA are evident in the bioinformatic analysis of the mitochondrial genomic DNA sequences of the five groups. Some of the highly-conserved and slightly-variated regions are identified in the mitochondrial cytochrome-c-oxidase subunit I (COI) gene, 16s ribosomal RNA (16s rRNA) gene, and 12s ribosomal RNA (12s rRNA) gene of these groups. To specify each five cephalopod groups, specific primer sets were designed from the COI, 16s rRNA and 12s rRNA regions. The specific primer sets amplified the DNA using the SYBR-green-based real-time PCR system and 11 commercially secured animal tissues: Octopus vulgaris, Octopus minor, Todarodes pacificus, Dosidicus gigas, Sepia esculenta, Amphioctopus fangsiao, Amphioctopus aegina, Amphioctopus marginatus, Loliolus beka, Loligo edulis, and Loligo chinensis. The results confirmed by a conveient way to calculate relative amplification levels between different samples in that it directly uses the threshold cycles (Ct)-value range generated by the qPCR system from these samples. This genomic DNA-based molecular technique provides a quick, accurate, and reliable method for the taxonomic classification of the animal tissues using the real-time qPCR.