2016
DOI: 10.1111/1755-0998.12601
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DNA barcodes of the native ray‐finned fishes in Taiwan

Abstract: Species identification based on the DNA sequence of a fragment of the cytochrome c oxidase subunit I gene in the mitochondrial genome, DNA barcoding, is widely applied to assist in sustainable exploitation of fish resources and the protection of fish biodiversity. The aim of this study was to establish a reliable barcoding reference database of the native ray-finned fishes in Taiwan. A total of 2993 individuals, belonging to 1245 species within 637 genera, 184 families and 29 orders of ray-finned fishes and re… Show more

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Cited by 73 publications
(50 citation statements)
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“…The COI gene has high base nitrogen of Adenosine and Thymine and high level of nucleotide variation. COI gene also can be used for the identification of marine nematode species (Derycke et al, 2010) and fish species (Chang et al, 2016).…”
Section: Figure 2 Dna Electrophoresis Results Of Coi Genementioning
confidence: 99%
“…The COI gene has high base nitrogen of Adenosine and Thymine and high level of nucleotide variation. COI gene also can be used for the identification of marine nematode species (Derycke et al, 2010) and fish species (Chang et al, 2016).…”
Section: Figure 2 Dna Electrophoresis Results Of Coi Genementioning
confidence: 99%
“…Some misidentifications are found in the sequences deposited in GenBank identified as different species of Chascanopsetta. For instance, the sequence KU945123 reported in Chang et al (2017) was associated with the specimen (specimen voucher: ASIZP 73836; tissue voucher: ASIZP 916333) collected from "Taiwan" and originally identified as "C. lugubris". However, according to the results of our molecular analysis, the sequence grouped with those from C. novaeguineae (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…Three mitochondrial markers (cytochrome c oxidase subunit 1 [ COI ]; 16S ribosomal RNA [ 16S ] and control region) were amplified using the polymerase chain reaction (PCR). Primer sets and PCR conditions followed those of Chang et al () for COI , Ahyong and Jarman () for 16S , and Cheng et al () for control region (Supplemental Table ). EconoTaq Master Mix (New England Biolabs, Massachusetts, USA) was used as a source of Taq polymerase, dNTPs, and reaction buffer for all PCR reactions.…”
Section: Methodsmentioning
confidence: 99%