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Articles

Phylogenetic position and ISSR-estimated intraspecific genetic variation of Bangia maxima (Bangiales, Rhodophyta)

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Pages 599-613 | Received 27 Jun 2007, Accepted 06 Aug 2008, Published online: 22 Apr 2019
 

Abstract

M.D.J. Lynch, R.G. Sheath2 and K.M. Müller. 2008. Phylogenetic position and ISSR-estimated intraspecific genetic variation of Bangia maxima (Bangiales, Rhodophyta). Phycologia 47: 599–613. DOI: 10.2216/07-47.1

The red alga Bangia maxima, in addition to its large size (up to 35 cm long × 6 mm in diameter), was found in this study to be distinguishable from other species of Bangia by the character of mature filament apices containing elongate, separated vegetative cells. The phylogenetic position of B. maxima was resolved using both the rbcL and nuclear small subunit rRNA (nSSU rRNA) gene sequences and the genetic variation within a population was studied using an inter-simple sequence repeat (ISSR) polymerase chain reaction (PCR)-based DNA fingerprint analysis. In phylogenetic analyses of the plastid rbcL gene region and nSSU rRNA, B. maxima grouped with local populations of concurrently collected B. vermicularis and B. fuscopurpurea as well as other collections of B. fuscopurpurea from California in a clade of predominantly eastern Pacific isolates. Banding patterns from 13 male filaments from seven littoral boulders for five ISSR primers were used to develop both band presence or absence and distance matrices (using the Dice coefficient). Banding patterns of B. maxima isolates were highly polymorphic among different boulders but consistent among individuals from the same boulder, as demonstrated by multivariate analyses (UPGMA, principal coordinates analysis). UPGMA analysis also indicated a limited genetic transfer among boulders. These results help in clarifying the population genetics of B. maxima and further understanding of genetic diversity within the Bangiales.

ACKNOWLEDGMENTS

This research was supported by NSERC (National Science and Engineering Research Council) and ERA (Ontario Early Researcher Award) funding to K.M.M., NSF (National Science Foundation) to K.M.M. and R.G.S. and an OGS (Ontario Graduate Scholarship) to M.D.J.L. Technical assistance in DNA sequencing from Mihaela Savelescu is greatly appreciated.

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