2016
DOI: 10.1098/rsos.160253
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Beyond the Coral Triangle: high genetic diversity and near panmixia in Singapore's populations of the broadcast spawning sea starProtoreaster nodosus

Abstract: The Coral Triangle is widely considered the most important centre of marine biodiversity in Asia while areas on its periphery such as the South China Sea, have received much less interest. Here, we demonstrate that a small population of the knobbly sea star Protoreaster nodosus in Singapore has similarly high levels of genetic diversity as comparable Indonesian populations from the Coral Triangle. The high genetic diversity of this population is remarkable because it is maintained despite decades of continued … Show more

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Cited by 20 publications
(24 citation statements)
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References 81 publications
(118 reference statements)
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“…Such confirmation is especially important for species complexes with suspected cryptic species (Ewers & Wares, 2012;Huang, Chen, Wei, Bu, & Wu, 2017;James et al, 2010;Yang et al, 2015). COI is particularly suitable for this purpose because it has broad taxon coverage due to its use in DNA barcoding and phylogeography (Crandall et al, 2008;Herbert, Cywinska, Ball, & deWaard, 2003;Tay et al, 2016). Moreover, data for large numbers of specimens can be readily obtained using multiplexed high-throughput sequencing DNA barcoding methods (Meier, Wong, Srivathsan, & Foo, 2016).…”
Section: Discussionmentioning
confidence: 99%
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“…Such confirmation is especially important for species complexes with suspected cryptic species (Ewers & Wares, 2012;Huang, Chen, Wei, Bu, & Wu, 2017;James et al, 2010;Yang et al, 2015). COI is particularly suitable for this purpose because it has broad taxon coverage due to its use in DNA barcoding and phylogeography (Crandall et al, 2008;Herbert, Cywinska, Ball, & deWaard, 2003;Tay et al, 2016). Moreover, data for large numbers of specimens can be readily obtained using multiplexed high-throughput sequencing DNA barcoding methods (Meier, Wong, Srivathsan, & Foo, 2016).…”
Section: Discussionmentioning
confidence: 99%
“…The ddRAD‐Seq libraries were prepared as in Tay et al. (), with modifications as follows: (1) magnetic bead‐PEG buffer suspension:DNA ratios were narrowed (0.81×, 0.95×), (2) PCR cycles were reduced from 18 to 16, and (3)an additional round of size selection on the pooled product was performed at the end to ensure a clean product. For pooling purposes, individuals from each sampling location had a unique Illumina Index, and each sample within those pools had a unique 5 bp barcode (Table ).…”
Section: Methodsmentioning
confidence: 99%
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“…We used combinatorial indices and barcodes derived from Peterson et al (2012) to uniquely identify each sequenced individual in our final multiplexed ddRAD-Seq library. Library preparation followed Tay et al (2016) with the following modifications: (i) 150 ng of DNA from each individual were simultaneously double-digested with restriction enzymes and ligated to adapters, in triplicate, and (ii) the targeted fragment size range was 250-650 bp. We followed the original protocol and PCR-amplified sizeselected DNA with 20 amplification cycles in triplicate before pooling replicate sample libraries and performing a second clean-up with size-selection to remove unannealed adapters and PCR primer dimers.…”
Section: Ddrad-seq Library Sequencingmentioning
confidence: 99%
“…Therefore, we randomly subsampled 338 tissue samples to be processed for DNA library preparation. For these samples, we used the methods of Tay et al (2016) to prepare 3 distinct ddRAD-seq libraries. The quality check of the final library fragment range was performed with a fragment analyzer automated capillary electrophoresis system (Advenced Analytical, Ankeny).…”
Section: Library Preparation and Sequencing Of Ddrad-seqmentioning
confidence: 99%