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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Testing DNA barcodes to help identify biodiversity hotspot plants including endangered and cryptic species

Plants challenge DNA barcoding. It has been difficult to identify candidate barcode regions that amplify readily and also distinguish among closely-related species. In 7 February 2008 PNAS (open access) researchers from University of Johannesburg; University of Costa Rica; Royal Botanic Gardens, Kew; and Imperial College, London, analyze potential barcode regions on specimens collected in plant biodiversity hotspots in Kruger National Park, South Africa, and Costa Rica. They initially tested eight candidate regions identified in earlier studies (coding regions accD, rpoC1, rpoB, ndhJ, ycf5, and matK, and non-coding trnH-psbA). Amplification was done according to earlier studies except that a different set of matK primers was used which appeared to be more effective. All eight regions were examined in 101 specimens representing 32 species of trees, shrubs, and achlorophyllous parasites from South Africa, and on 71 specimens representing 48 species of Costa Rican orchids (in all, 44 species with 2-7 specimens per species, and 36 species with one sample). Based on their analysis, the coding region matK with the new primer set and the non-coding region trnH-psbA were >90% effective in species identification. For reasons I do not understand, the authors favor unweighted pair group method with arithmetic mean (UPGMA) for analyzing genetic clustering, although they tested neighbor-joining, maximum likelihood, maximum parsimony, and Bayesian methods. Given the presumed advantages of a coding region barcode (ease of alignment, greater higher-level phylogenetic signal), Lahaye et al propose 5′ region of plastid gene matK as a first-pass standard barcode for plants.  

The authors then analyzed the 5′ matK barcode in a much larger sample of orchids: 1,566 specimens representing 1,084 Mesoamerican species. It is exciting that this is the largest test of candidate barcode variation within species for plants to date. They report 212 genetic clusters in UPGMA tree, of which “86 fully matched previously recognized species and a further 25 partially matched taxonomic species…an examination of these clusters reveals cryptic species, which need further taxonomic work”. I am unsure from this short report what “partially matched taxonomic species” are and how many possible cryptic species were identified. I look forward to a more detailed report on the DNA barcodes, morphology, and range distribution of this very large sample of Mesoamerican orchids.  A DNA-based method for identifying non-flowering orchids and other plants could help protect many threatened species. 

This entry was posted on Monday, February 18th, 2008 at 10:23 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 “Testing DNA barcodes to help identify biodiversity hotspot plants including endangered and cryptic species”

  1. Mark Stoeckle Says:

    A concise, comprehensive review of plant barcoding results so far, including where Lahaye et al’s work fits in this context, is in this same issue 26 February PNAS http://www.pnas.org/cgi/reprint/0800476105v1, authors Kress and Erickson, Smithsonian Institution.

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.