The Barcode Blog

A mostly scientific blog about short DNA sequences for species identification and discovery. I encourage your commentary. -- Mark Stoeckle

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Deepwater clam mtDNAs map in unexplored sequence territory

Approximately 8,000 – 15,000 species of bivalves (clams, mussels, scallops, oysters, and relatives) are known. According to BOLD Taxonomy Browser www.barcodinglife.org, 620 bivalve species have COI barcode records so far, so this group is relatively unexplored genetically. In September 2007 Zoologica Scripta researchers from University of Bergen, Norway, analyze COI barcode region sequences of 62 deepwater clams dredged in a single offshore region at 69 m to 567 m, morphologically identified as 12 species from 4 genera (Thyasira, Ennucula, Nucula, Yoldiella) representing 3 subclasses of Bivalvia. The COI barcode region was amplified with broad-range primers (Folmer et al 1994). Mean differences within species collected in this single area were small, 0.0 – 0.48%, similar to results in other animal groups, suggesting assignment of specimens to species will be straightforward. This will be helpful in environmental surveys for example, as some species “are infamous for being difficult to determine to species from morphology” and some “remain difficult to identify for the non-expert.” As one example, some Thyasira species are distinguished only by sperm and egg morphology, which is impractical in most circumstances.

https://www.conchology.be/en/home/home.phpmtDNA differences among these bivalves are remarkably large, even among species in the same genus. The differences among congeneric species in this sample (average 22%, range 12-42%) are larger than differences among entire class Aves (according to my analysis with BOLD software, COI differences among birds in different orders, such as penguins and hummingbirds for example, average 20%, with range 14-28%).

Blastn GenBank searches with these divergent mtDNA sequences showed very limited identity to anything, and the closest matches were short stretches (100-150 nucleotides of the 678 full-length barcode sequence) to COI sequences of species outside the phylum Mollusca (I obtained similar results submitting Thyasira sequences for example to the public BOLD Identification Engine at www.barcodinglife.org.)  It will be helpful if Mikkelsen et al deposit their sequences along with associated collecting data (voucher specimen information, images, collection locations) to the BOLD database. I look forward to learning more about these bivalves, and whether their remarkably deep differences in mtDNA are associated with deep physiological, ecological, or other biological differences.

This entry was posted on Friday, February 8th, 2008 at 3:20 pm and is filed under General. You can follow any responses to this entry through the RSS 2.0 feed. Both comments and pings are currently closed.

One Response to “Deepwater clam mtDNAs map in unexplored sequence territory”

  1. Unblock myspace Says:

    Doing a school project on mtDNA, thanks for this.

Contact: mark.stoeckle@rockefeller.edu

About this site

This web site is an outgrowth of the Taxonomy, DNA, and Barcode of Life meeting held at Banbury Center, Cold Spring Harbor Laboratory, September 9-12, 2003. It is designed and managed by Mark Stoeckle, Perrin Meyer, and Jason Yung at the Program for the Human Environment (PHE) at The Rockefeller University.

About the Program for the Human Environment

The involvement of the Program for the Human Environment in DNA barcoding dates to Jesse Ausubel's attendance in February 2002 at a conference in Nova Scotia organized by the Canadian Center for Marine Biodiversity. At the conference, Paul Hebert presented for the first time his concept of large-scale DNA barcoding for species identification. Impressed by the potential for this technology to address difficult challenges in the Census of Marine Life, Jesse agreed with Paul on encouraging a conference to explore the contribution taxonomy and DNA could make to the Census as well as other large-scale terrestrial efforts. In his capacity as a Program Director of the Sloan Foundation, Jesse turned to the Banbury Conference Center of Cold Spring Harbor Laboratory, whose leader Jan Witkowski prepared a strong proposal to explore both the scientific reliability of barcoding and the processes that might bring it to broad application. Concurrently, PHE researcher Mark Stoeckle began to work with the Hebert lab on analytic studies of barcoding in birds. Our involvement in barcoding now takes 3 forms: assisting the organizational development of the Consortium for the Barcode of Life and the Barcode of Life Initiative; contributing to the scientific development of the field, especially by studies in birds, and contributing to public understanding of the science and technology of barcoding and its applications through improved visualization techniques and preparation of brochures and other broadly accessible means, including this website. While the Sloan Foundation continues to support CBOL through a grant to the Smithsonian Institution, it does not provide financial support for barcoding research itself or support to the PHE for its research in this field.