2001
DOI: 10.2307/3761655
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[beta]-Tubulin, ITS and Group I Intron Sequences Challenge the Species Pair Concept in Physcia aipolia and P. caesia

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Cited by 95 publications
(61 citation statements)
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“…These results suggests a strong geographical structure in the L. retigera lineage, among the populations in Canada, Madagascar, Bhutan, Yunnan (China), and Sakhalin (Russia), of this widely distributed taxon. It is likely that these isolated populations have evolved over geologically long periods, and, independent of their reproductive mode and taxonomic rank, these geographically differentiated clades may deserve the status of evolutionarily significant units (Moritz 1995) (Lohtander et al 1998a, b;Myllys et al 1999;Myllys et al 2001), our study of L. retigera shows that apotheciate clades have developed repeatedly from rarely fertile, isidiate morphs. In contrast to Poelt's (1972) hypothesis of species pairs, published studies reveal transitions from isidiate morphs that have the potential to form apothecia rarely, towards apotheciate morphs that produce no vegetative propagules.…”
Section: Discussionmentioning
confidence: 66%
“…These results suggests a strong geographical structure in the L. retigera lineage, among the populations in Canada, Madagascar, Bhutan, Yunnan (China), and Sakhalin (Russia), of this widely distributed taxon. It is likely that these isolated populations have evolved over geologically long periods, and, independent of their reproductive mode and taxonomic rank, these geographically differentiated clades may deserve the status of evolutionarily significant units (Moritz 1995) (Lohtander et al 1998a, b;Myllys et al 1999;Myllys et al 2001), our study of L. retigera shows that apotheciate clades have developed repeatedly from rarely fertile, isidiate morphs. In contrast to Poelt's (1972) hypothesis of species pairs, published studies reveal transitions from isidiate morphs that have the potential to form apothecia rarely, towards apotheciate morphs that produce no vegetative propagules.…”
Section: Discussionmentioning
confidence: 66%
“…We used the primers Mcm7-709for and Mcm7-1348rev (Schmitt et al 2009) for amplification of the Mcm7 region and in some cases we carried out a nested PCR using 1 μl of the PCR product and the internal primers Mcm7-CalicF and Mcm7-CalicR . The protein coding β-tubulin was amplified using the primers Bt3-LM and Bt10-LM (Myllys et al 2001).…”
Section: Molecular Techniquesmentioning
confidence: 99%
“…The protein coding Beta-tubulin gene was amplified using the 9 primers Bt3-LM, B10-LM (Myllys et al, 2001) and the newly designed Collemataceae primers BetaCollF (AGGCATCTGGAAACAAATATGT) and BetaCollR (GCGCCACGGCTTGTCAACG); and the locus MCM7 using the primers MCM7-709 and MCM7 1348 (Schmitt et al, 2009b). PCR amplifications were performed using Illustra TM Hot…”
Section: Dna Sequencingmentioning
confidence: 99%
“…The nrLSU rDNA was amplified using the primers LR7 (Vilgalys and Hester, 1990), nrLSU 0170-R (Otálora et al, 2010) and the newly designed Collemataceae primers LR500CollF (ACCAAGGAGTCTAACGTCCCCG) and LR1200CollR (CATTCGGCCGGTGAGCTGTTACG); mtSSU rDNA using the primers mtSSU1 and mtSSU3R (Zoller et al, 1999). The protein coding Beta-tubulin gene was amplified using the primers Bt3-LM, B10-LM (Myllys et al, 2001) and the newly designed Collemataceae primers BetaCollF (AGGCATCTGGAAACAAATATGT) and BetaCollR (GCGCCACGGCTTGTCAACG); and the locus MCM7 using the primers MCM7-709 and MCM7 1348 (Schmitt et al, 2009b). PCR amplifications were performed using Illustra TM Hot…”
Section: Dna Sequencingmentioning
confidence: 99%