2020
DOI: 10.1002/lom3.10387
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Comparison of visual and molecular taxonomic methods to identify ichthyoplankton in the North Sea

Abstract: The North Sea is an important spawning and nursery ground for many demersal and pelagic fishes whose spawning areas are largely overlapping in time and space. This makes ichthyoplankton visual identification from the various species particularly challenging. Despite historically intensive research in the area, detailed information on spawning sites and times for many taxa, are incomplete. To update and detail the mapping of fish spawning performance and distribution in the central and northern regions of the N… Show more

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Cited by 12 publications
(5 citation statements)
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“…DNA from eggs was isolated as described by Mateos‐Rivera et al. ( 2020 ), while cod tissue was suspended in lysis buffer from the DNAdvance kit (Beckman Coulter, CA, USA) and processed using a Biomek i5 Automated Workstation (Beckman Coulter), following the manufacturer's instructions.…”
Section: Methodsmentioning
confidence: 99%
“…DNA from eggs was isolated as described by Mateos‐Rivera et al. ( 2020 ), while cod tissue was suspended in lysis buffer from the DNAdvance kit (Beckman Coulter, CA, USA) and processed using a Biomek i5 Automated Workstation (Beckman Coulter), following the manufacturer's instructions.…”
Section: Methodsmentioning
confidence: 99%
“…Both mtDNA genes were amplified in a 15‐μL PCR mix consisting of 1x Buffer, 2 mM MgCl 2 , 0.15 mM dNTP, 1 U GoTaq polymerase (Promega), 0.4 μM of each primer, and 3 μL of the template. PCR amplification was performed at 95°C; 35 cycles of 94°C for 30 s, 48°C for 30 s, 72°C for 1 min; and 72°C 7 min; and purified following the procedure described in Mateos‐Rivera et al ( 2020 ), before being sent for sequencing in duplicates (one per each direction) to Eurofins Genomics.…”
Section: Methodsmentioning
confidence: 99%
“…Afterwards, 50 μL of the neutralizing solution (Tris-HCl 40 mM, pH 5) were added to the mixture. Upon DNA isolation, PCR amplification targeting the mitochondrial COI gene was performed following the methods described in Mateos-Rivera et al (2020). We refer to Table S1 for details on PCR amplification, purification, and sequencing.…”
Section: Morphological and Molecular Taxonomic Methodsmentioning
confidence: 99%