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		<title>Publications by J. Lima</title>
		<link>http://cfs.nrcan.gc.ca/authors/read/22631?format=title&amp;lang=en_CA</link>
		<description>Publications by J. Lima</description>
		<language>en-ca</language>
		<pubDate>2011-03-22 11:57:54 MST</pubDate>
		<lastBuildDate>2011-03-22 11:57:54 MST</lastBuildDate>
		<webMaster>webmaster@nofc.cfs.nrcan.gc.ca</webMaster>
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			<title>Common goals: policy implications of DNA barcoding as a protocol for identification of arthropod pests</title>
			<link>http://cfs.nrcan.gc.ca/publications?id=32223</link>
			<description>The globalization of commerce carries with it significant biological risks concerning the spread of harmful organisms. International Standards for Phytosanitary Measures (ISPM) No. 27, ‘‘Diagnostic Protocols for Regulated Pests’’, sets out the standards governing protocols for the detection and identification of plant pest species. We argue that DNA barcoding—the use of short, standardized DNA sequences for species identification—is a methodology which should be incorporated into standard diagnostic protocols, as it holds great promise for the rapid identification of species of economic importance, notably arthropods. With a well-defined set of techniques and rigorous standards of data quality and transparency, DNA barcoding already meets or exceeds the minimum standards required for diagnostic protocols under ISPM No. 27. We illustrate the relevance of DNA barcoding to phytosanitary concerns and advocate the development of policy at the national and international levels to expand the scope of barcode coverage for arthropods globally.</description>
			<pubDate>Tue, 22 Mar 2011</pubDate>
			<guid>http://cfs.nrcan.gc.ca/publications?id=32223</guid>
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			<title>Towards a Global Barcode Library for Lymantria (Lepidoptera: Lymantriinae) Tussock Moths of Biosecurity Concern</title>
			<link>http://cfs.nrcan.gc.ca/publications?id=32217</link>
			<description>Background
Detecting and controlling the movements of invasive species, such as insect pests, relies upon rapid and accurate species identification in order to initiate containment procedures by the appropriate authorities. Many species in the tussock moth genus Lymantria are significant forestry pests, including the gypsy moth Lymantria dispar L., and consequently have been a focus for the development of molecular diagnostic tools to assist in identifying species and source populations. In this study we expand the taxonomic and geographic coverage of the DNA barcode reference library, and further test the utility of this diagnostic method, both for species/subspecies assignment and for determination of geographic provenance of populations.&lt;/p&gt;

&lt;p&gt;Methodology/Principal Findings
Cytochrome oxidase I (COI) barcodes were obtained from 518 individuals and 36 species of Lymantria, including sequences assembled and generated from previous studies, vouchered material in public collections, and intercepted specimens obtained from surveillance programs in Canada. A maximum likelihood tree was constructed, revealing high bootstrap support for 90% of species clusters. Bayesian species assignment was also tested, and resulted in correct assignment to species and subspecies in all instances. The performance of barcoding was also compared against the commonly employed NB restriction digest system (also based on COI); while the latter is informative for discriminating gypsy moth subspecies, COI barcode sequences provide greater resolution and generality by encompassing a greater number of haplotypes across all Lymantria species, none shared between species.&lt;/p&gt;

&lt;p&gt;Conclusions/Significance
This study demonstrates the efficacy of DNA barcodes for diagnosing species of Lymantria and reinforces the view that the approach is an under-utilized resource with substantial potential for biosecurity and surveillance. Biomonitoring agencies currently employing the NB restriction digest system would gather more information by transitioning to the use of DNA barcoding, a change which could be made relatively seamlessly as the same gene region underlies both protocols.</description>
			<pubDate>Mon, 21 Mar 2011</pubDate>
			<guid>http://cfs.nrcan.gc.ca/publications?id=32217</guid>
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