2007
DOI: 10.1590/s1519-69842007000500016
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Population analysis of Scomberomorus cavalla (Cuvier, 1829) (Perciformes, Scombridae) from the Northern and Northeastern coast of Brazil

Abstract: Scomberomorus cavalla is a pelagic fish species widely distributed on the Atlantic west coast, and a noticeable decrease in its capture level in the USA and Gulf of Mexico is occurring, compared to the levels reached by the species in the past. Likewise, in some areas of Brazil, there has been indication of over-harvesting. However, there are no molecular studies focusing on the management of such an important item. Thus, in the present study, 380 nucleotide base pairs of the mitochondrial DNA D-Loop region of… Show more

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Cited by 19 publications
(17 citation statements)
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“…The estimated levels of genetic variation are consistent with large populations and are quite similar to that of the congeneric species S. sierra ( h = 0·997, π = 0·019) and Scomberomorus maculatus (Mitchill 1815) ( h = 0·812, π = 0·026) for sequences of the mtDNA‐CR and nicotinamide adenine dinucleotide (NADH), respectively (Buonaccorsi et al , ; Domínguez‐López et al , ); however, the estimated variation was higher than that reported in the mtDNA‐CR of S. cavalla ( h = 0·704, π = 0·005; Santa Brígida et al , ).…”
Section: Scomberomorus Concolor Sample Locations Summary Statistics supporting
confidence: 67%
“…The estimated levels of genetic variation are consistent with large populations and are quite similar to that of the congeneric species S. sierra ( h = 0·997, π = 0·019) and Scomberomorus maculatus (Mitchill 1815) ( h = 0·812, π = 0·026) for sequences of the mtDNA‐CR and nicotinamide adenine dinucleotide (NADH), respectively (Buonaccorsi et al , ; Domínguez‐López et al , ); however, the estimated variation was higher than that reported in the mtDNA‐CR of S. cavalla ( h = 0·704, π = 0·005; Santa Brígida et al , ).…”
Section: Scomberomorus Concolor Sample Locations Summary Statistics supporting
confidence: 67%
“…The mitochondrial Control Region was amplified using the primers L1 (5′‐CCTAACTCCCAAAGCTAGGTATTC‐3′) and H2 (5′‐ TGTTTATCACTGCTGRRTTCCCT‐3′), described by Santa Brígida et al. (). The PCRs were prepared in a final volume of 25 μl containing: 2.5 μl Buffer (20 mM Tris‐HCl), 4 μl of dNTPs (1.25 mM), 1 μl of MgCl 2 (50 mM), 1–1.5 μl of DNA (approximately 50 ng), 0.25 μl (200 ng/μl) of each primer, 0.2 μl of 1 U Taq polymerase (5 U/μl, Invitrogen, Carlsbad, USA), with water being added to complete the final reaction volume.…”
Section: Methodsmentioning
confidence: 99%
“…The mitochondrial Control Region was isolated and amplified using the Polymerase Chain Reaction (PCR) based on the primers D-LoopL1 '5 CTAACTCCCAAAGCTAGGTATTC3' and D-LoopH1 '5 TGTTTATCACTGCTGRRTTCCCT 3' (Santa Brígida et al, 2007). The PCR was run in a final volume of 25 µl composed of 4 μl of DNTPs (1.25 M), 2.5 μl of buffer solution (10X), 0.5 μl of MgCl 2 solution (50 mM), 1 μl of DNA (250 ng/μl), 0.25 μl of each primer (200 ng/μl), 0.2 μl of the Taq polymerase enzyme (5U/μl), and 16.3 μl of purified water.…”
Section: Pcr and Sequencingmentioning
confidence: 99%