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Identification of the vascular plants of Churchill, Manitoba, using a DNA barcode library
BACKGROUND: Because arctic plant communities are highly vulnerable to climate change, shifts in their composition require rapid, accurate identifications, often for specimens that lack diagnostic floral characters. The present study examines the role that DNA barcoding can play in aiding floristic e...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538695/ https://www.ncbi.nlm.nih.gov/pubmed/23190419 http://dx.doi.org/10.1186/1472-6785-12-25 |
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author | Kuzmina, Maria L Johnson, Karen L Barron, Hannah R Hebert, Paul DN |
author_facet | Kuzmina, Maria L Johnson, Karen L Barron, Hannah R Hebert, Paul DN |
author_sort | Kuzmina, Maria L |
collection | PubMed |
description | BACKGROUND: Because arctic plant communities are highly vulnerable to climate change, shifts in their composition require rapid, accurate identifications, often for specimens that lack diagnostic floral characters. The present study examines the role that DNA barcoding can play in aiding floristic evaluations in the arctic by testing the effectiveness of the core plant barcode regions (rbcL, matK) and a supplemental ribosomal DNA (ITS2) marker for a well-studied flora near Churchill, Manitoba. RESULTS: This investigation examined 900 specimens representing 312 of the 354 species of vascular plants known from Churchill. Sequencing success was high for rbcL: 95% for fresh specimens and 85% for herbarium samples (mean age 20 years). ITS2 worked equally well for the fresh and herbarium material (89% and 88%). However, sequencing success was lower for matK, despite two rounds of PCR amplification, which reflected less effective primer binding and sensitivity to the DNA degradation (76% of fresh, 45% of herbaria samples). A species was considered as taxonomically resolved if its members showed at least one diagnostic difference from any other taxon in the study and formed a monophyletic clade. The highest species resolution (69%) was obtained by combining information from all three genes. The joint sequence information for rbcL and matK distinguished 54% of 286 species, while rbcL and ITS2 distinguished 63% of 285 species. Discrimination of species within Salix, which constituted 8% of the flora, was particularly problematic. Despite incomplete resolution, the barcode results revealed 22 misidentified herbarium specimens, and enabled the identification of field specimens which were otherwise too immature to identify. Although seven cases of ITS2 paralogy were noted in the families Cyperaceae, Juncaceae and Juncaginaceae, this intergenic spacer played an important role in resolving congeneric plant species at Churchill. CONCLUSIONS: Our results provided fast and cost-effective solution to create a comprehensive, effective DNA barcode reference library for a local flora. |
format | Online Article Text |
id | pubmed-3538695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35386952013-01-10 Identification of the vascular plants of Churchill, Manitoba, using a DNA barcode library Kuzmina, Maria L Johnson, Karen L Barron, Hannah R Hebert, Paul DN BMC Ecol Methodology Article BACKGROUND: Because arctic plant communities are highly vulnerable to climate change, shifts in their composition require rapid, accurate identifications, often for specimens that lack diagnostic floral characters. The present study examines the role that DNA barcoding can play in aiding floristic evaluations in the arctic by testing the effectiveness of the core plant barcode regions (rbcL, matK) and a supplemental ribosomal DNA (ITS2) marker for a well-studied flora near Churchill, Manitoba. RESULTS: This investigation examined 900 specimens representing 312 of the 354 species of vascular plants known from Churchill. Sequencing success was high for rbcL: 95% for fresh specimens and 85% for herbarium samples (mean age 20 years). ITS2 worked equally well for the fresh and herbarium material (89% and 88%). However, sequencing success was lower for matK, despite two rounds of PCR amplification, which reflected less effective primer binding and sensitivity to the DNA degradation (76% of fresh, 45% of herbaria samples). A species was considered as taxonomically resolved if its members showed at least one diagnostic difference from any other taxon in the study and formed a monophyletic clade. The highest species resolution (69%) was obtained by combining information from all three genes. The joint sequence information for rbcL and matK distinguished 54% of 286 species, while rbcL and ITS2 distinguished 63% of 285 species. Discrimination of species within Salix, which constituted 8% of the flora, was particularly problematic. Despite incomplete resolution, the barcode results revealed 22 misidentified herbarium specimens, and enabled the identification of field specimens which were otherwise too immature to identify. Although seven cases of ITS2 paralogy were noted in the families Cyperaceae, Juncaceae and Juncaginaceae, this intergenic spacer played an important role in resolving congeneric plant species at Churchill. CONCLUSIONS: Our results provided fast and cost-effective solution to create a comprehensive, effective DNA barcode reference library for a local flora. BioMed Central 2012-11-28 /pmc/articles/PMC3538695/ /pubmed/23190419 http://dx.doi.org/10.1186/1472-6785-12-25 Text en Copyright ©2012 Kuzmina et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Kuzmina, Maria L Johnson, Karen L Barron, Hannah R Hebert, Paul DN Identification of the vascular plants of Churchill, Manitoba, using a DNA barcode library |
title | Identification of the vascular plants of Churchill, Manitoba, using a DNA barcode library |
title_full | Identification of the vascular plants of Churchill, Manitoba, using a DNA barcode library |
title_fullStr | Identification of the vascular plants of Churchill, Manitoba, using a DNA barcode library |
title_full_unstemmed | Identification of the vascular plants of Churchill, Manitoba, using a DNA barcode library |
title_short | Identification of the vascular plants of Churchill, Manitoba, using a DNA barcode library |
title_sort | identification of the vascular plants of churchill, manitoba, using a dna barcode library |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538695/ https://www.ncbi.nlm.nih.gov/pubmed/23190419 http://dx.doi.org/10.1186/1472-6785-12-25 |
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