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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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Labelling specimens and species with standardized DNA sequences

Labelling specimens helps make natural history museum collections valuable. Once specimens have been carefully examined by an expert, a species label can be applied. Labelled specimens can then be re-found and re-examined. Unsorted specimens lacking species designations are more raw material than scientific resource.  

As in all sciences, taxonomic knowledge undergoes continuous revision. Changes in names and understanding of species boundaries may mean that specimen labels need to be updated in light of current knowledge. Partly to compensate, there is enormous effort to link current taxonomic understanding to historical species descriptions. Nonetheless, the accuracy of specimen labels may decay over time. In one study, a revision of predatory flies (Euscelidia) (Meier and Dikow Conservation Biol 2004 18:478), 83% of 1383 specimens from 19 collections were found to be incorrectly identified.

DNA sequences offer a simple approach to help keep specimen labels up to date. DNA sequences are an intrinsic, unvarying characteristic of a specimen. A DNA sequence from a standardized locus (ie a DNA barcode) can serve as a permanent “name” for a specimen. Results so far with more than 20,000 invertebrate and vertebrate species show it is generally straightforward to use a COI barcode to assign specimens to known species. Future taxonomic revisions may change species names or boundaries, but that will not change DNA barcodes of specimens or the clustering patterns of barcode sequences. Thus it should be simple to use a specimen’s barcode sequence “name” to search a regularly revised public database for the current species name it corresponds to. A public database of sequences, specimens, and associated data as is BOLD can undergo continuous refinement, whereas revising labels in every collection around the world is impractical. Given that assigning specimens to species involves sorting among millions of species names, this approach does not have to give 100% resolution to species level to be valuable. It will be useful both for those species with unique barcode clusters or characters and for those sets of closely-related species with overlapping or indistinguishable barcodes.

Finally, on a related note I observe that diagnostic keys are unwieldy and not easily amenable to computerization. For example, Dragonflies of North America (Gainesville: Scientific Publishers, 2000) by Needham, Westfall, and May covers 350 species in 939 pages, or about 2.7 pages per species, which by my count is typical for diagnostic keys. At this rate, a world key for the 5500 known Odonates would run to 15,000 pages. The recondite language that is required to describe morphologic detail in this and other keys makes the tools inacessible except to highly-trained persons.  On the other hand, anyone can interpret a DNA sequence. It is exciting that taxonomists and others are increasingly taking up the challenge of translating taxonomic knowledge into a much more widely-accessible format, namely DNA barcode libraries.

This entry was posted on Tuesday, December 12th, 2006 at 11:48 pm and is filed under General. You can follow any responses to this entry through the RSS 2.0 feed. You can leave a response, or trackback from your own site.

One Response to “Labelling specimens and species with standardized DNA sequences”

  1. cephalopodcast.com » Blog Archive » Curiosities of Biological Nomenclature Says:

    [...] I am sure it’s in there somewhere, but one of my favorites is the Jackknife fish (Equetus lanceolatus). There is also the recent classification of several slime-mold beetles named after Bush, Cheney and Rumsfeld and another beetle after Darth Vader. Of course some folks argue that a little less frivolity and a little more serious abstraction is needed in regards to classification. [...]

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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.