2017
DOI: 10.1007/s12526-017-0775-3
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First records of Geodia demosponges from the New England seamounts, an opportunity to test the use of DNA mini-barcodes on museum specimens

Abstract: We report the first records of the sponge genus Geodia (Demospongiae, Tetractinellida, Geodiidae) from the New England Seamounts and Muir Seamount, at lower bathyal depths. Nine specimens collected between 2000 and 2005 belong to two boreal species (Geodia macandrewii and Geodia barretti) and a temperate species (Geodia megastrella). These records extend the distributions of these deep-sea amphi-Atlantic species to the west. Most of these specimens were originally fixed in formalin, which substantially degrade… Show more

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Cited by 18 publications
(12 citation statements)
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“…Due to the formalin fixation, we were not able to extract DNA for molecular analysis, and any attempts to barcode the mitochondrial COI gene, including the mini-barcode protocol used in other tetractinellids (Cárdenas & Moore, 2017) were unsuccessful.…”
Section: Methodsmentioning
confidence: 99%
“…Due to the formalin fixation, we were not able to extract DNA for molecular analysis, and any attempts to barcode the mitochondrial COI gene, including the mini-barcode protocol used in other tetractinellids (Cárdenas & Moore, 2017) were unsuccessful.…”
Section: Methodsmentioning
confidence: 99%
“…Short DNA markers, so-called minimalist DNA barcodes (Hajibabaei et al 2006), can facilitate genotype comparison with degenerated type material using the Sanger sequencing methods if other methods for full-length amplification fail. Such minimalist DNA regions, which are sufficiently short for amplification from fragmented DNA templates but sufficiently variable for taxonomic distinction, are sequenced and analyzed (Cárdenas and Moore 2017).…”
Section: Introductionmentioning
confidence: 99%
“…For one specimen from Cape Verde (RMNH 3810) collected in 1982, the DNA was fairly degraded so we decided to amplify COI in two parts. For the first part we amplified the universal mini-barcode (130 bp) using primer pair LCO/Tetract-minibarR1 following the protocol from Cárdenas & Moore (2018). For the rest of the Folmer fragment we designed a forward primer in the mini-barcode to target Erylus species-ErylusCOI-F2 (5'-CTCCYGGATCAATGTTGGG-3')-and coupled it with HCO2198 always using the same COI PCR program.…”
Section: Introductionmentioning
confidence: 99%