Skip to main content
Log in

Chloroplast DNA-relationship in palaeoaustralLopidium concinnum (Hypopterygiaceae, Musci). An example of stenoevolution in mosses Studies in austral temperate rain forest bryophytes 2

  • Published:
Plant Systematics and Evolution Aims and scope Submit manuscript

Abstract

Evolutionary relationship between disjunct populations of the palaeoaustral moss taxonLopidium concinnum (Hypopterygiaceae) from New Zealand and southern South America were studied using non-coding chloroplast DNA sequences. No or only slight changes could be observed within the sequences oftrnTUGUtrnLUAA 5′exon intergenic spacer,trnLUAA intron andtrnLUAA 3′exon —trnFGAA intergenic spacer. This indicates nearly no genetic divergence between extant New Zealand and Chilean populations, i.e. no significant differing pathways of evolution within the 80–60 million years of disrupted areas with interrupted gene flow. Molecular data support the idea of an old Gondwanan relict species of stenoevolutionary character. Ecological data on short-range dispersal strengthen this assessment.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Böhle U.-R., Hilger H. H., Cerff R., Martin W. (1994) Noncoding chloroplast DNA for plant molecular systematics at the infrageneric level. In: Schierwater B., Streit G. P., Desalle R. (eds.) Molecular ecology and evolution: approaches and applications. Birkhäuser, Basel, pp. 391–403.

    Google Scholar 

  • Böhle U.-R., Hilger H. H., Martin W. (1996) Island colonization and evolution of the insular woody habit inEchium L. (Boraginaceae). Proc. Natl. Acad. Sci. USA 93: 11740–11745.

    PubMed  Google Scholar 

  • Doyle J. J., Doyle J. L. (1990) Isolation of plant DNA from fresh tissue. Focus 12: 13–15.

    Google Scholar 

  • Fangan B. M., Stedje B., Stabbetorp O. E., Jensen E. S., Jakobsen K. S. (1994) A general approach for PCR-amplification and sequencing of chloroplast DNA from crude vascular plant and algal tissue. BioTechniques 16: 484–494.

    PubMed  Google Scholar 

  • Frey W. (1990) Genoelemente prä-angiospermen Ursprungs bei Bryophyten. Bot. Jahrb. Syst. 111: 433–456.

    Google Scholar 

  • Frey W., Beever J. E. (1995) Dendroid bryophyte communities of New Zealand. Nova Hedwigia 61: 323–354.

    Google Scholar 

  • Galloway D. J. (1991) Phytogeography of Southern Hemisphere lichens. In: Nimis P. L., Crovello T. J. (eds.) Quantitative approaches to phytogeography. Kluwer, Dordrecht, pp. 233–262.

    Google Scholar 

  • Galloway D. J., Jørgensen P. M. (1987) Studies in the lichen familyPannariaceae II. The genusLeioderma NYL. Lichenologist 19: 345–400.

    Google Scholar 

  • Gielly L., Taberlet P. (1994) The use of chloroplast DNA to resolve plant phylogenies: Noncoding versusrbcL sequences. Molec. Biol. Evol. 11: 769–777.

    PubMed  Google Scholar 

  • Gielly L., Taberlet P. (1996a) Chloroplast DNA sequencing to resolve plant phylogenies between closely related taxa. In: Smith T. B., Wayne R. K. (eds.) Molecular genetic approaches in conservation. Oxford University Press, New York, pp. 143–153.

    Google Scholar 

  • Gielly L., Taberlet P. (1996b) A phylogeny of European gentians inferred from chloroplasttrnL (UAA) intron sequences. Bot. J. Linn. Soc. 120: 57–75.

    Google Scholar 

  • Ham R. C. H. J. van, 't Hart H., Mes T. H. M., Sandbrink J. M. (1994) Molecular evolution of noncoding regions of the chloroplast genome in theCrassulaceae and related species. Curr. Genet. 25: 558–566.

    PubMed  Google Scholar 

  • Hampe E. (1879) Enumeratio muscorum frondosorum Brasiliae centralis, praecipue provinciarum Rio de Janeiro et S. Paulo, adhuc cognitorum. Vidensk. Meddel. Dansk Naturhist. Foren. Kjøbenhavn, Ser. 4, 1: 162.

    Google Scholar 

  • Kuhsel M. G., Strickland R., Palmer J. D. (1990) An ancient group I intron shared by eubacteria and chloroplasts. Science 250: 1570–1573.

    PubMed  Google Scholar 

  • Matteri C. M. (1973) Revision de lasHypopterygiaceae (Musci) Austrosudamericanas. Bol. Soc. Argentina Bot. 15: 229–250.

    Google Scholar 

  • Mes T. H. M., van Brederode J., 't Hart H. (1996) Origin of the woody MacaronesianSempervivoideae and the phylogenetic position of the East African species ofAeonium. Bot. Acta 109: 477–491.

    Google Scholar 

  • Miller H. A. (1982) Bryophyte evolution and geography. Biol. J. Linn. Soc. 18: 145–196.

    Google Scholar 

  • Ohyama K., Fukuzawa H., Kohchi T., Shirai H., Sano T., Umesono K., Shiki Y., Takeuchi M., Chang Z., Aota S., Inokuchi H., Ozeki H. (1986) Chloroplast gene organisation deduced from complete sequence of liverwortMarchantia polymorpha chloroplast DNA. Nature 32: 572–574.

    Google Scholar 

  • Schuster R. M. (1979) On the persistence and dispersal of transantarcticHepaticae. Canad. J. Bot. 57: 2179–2225.

    Google Scholar 

  • Schuster R. M. (1982) Generic and familial endemisms in the Hepatic flora of Gondwana land: origins and causes. J. Hattori Bot. Lab. 52: 3–35.

    Google Scholar 

  • Schuster R. M. (1983) Phytogeography of theBryophyta. In: Schuster R. M. (ed.) New Manual of Bryology 1: 463–626. Hattori Botanical Laboratory, Nichinan.

    Google Scholar 

  • Schuster R. M. (1988) Ecology, reproductive biology and dispersal ofHepaticae in the tropics. J. Hattori Bot. Lab. 64: 237–269.

    Google Scholar 

  • Taberlet P., Gielly L., Pautou G., Bouvet J. (1991) Universal primers for amplification of three non-coding regions of chloroplast DNA. Pl. Molec. Biol. 17: 1105–1109.

    Google Scholar 

  • Thériot I. (1934) Quelques mousses du Chili austral récoltées à freire par Mr. R. Gillet L., en fevrier 1934. Revista Chilena Hist. Nat. 38: 83–85.

    Google Scholar 

  • White M. E. (1990) The flowering of Gondwana. Princeton University Press, Princeton.

    Google Scholar 

  • Zanten B. O. van (1978) Experimental studies on transoceanic long-range dispersal of moss spores in the Southern Hemisphere. J. Hattori Bot. Lab. 44: 455–482.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Frey, W., Stech, M. & Meissner, K. Chloroplast DNA-relationship in palaeoaustralLopidium concinnum (Hypopterygiaceae, Musci). An example of stenoevolution in mosses Studies in austral temperate rain forest bryophytes 2. Pl Syst Evol 218, 67–75 (1999). https://doi.org/10.1007/BF01087035

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01087035

Key words

Navigation