Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Australian Systematic Botany Australian Systematic Botany Society
Taxonomy, biogeography and evolution of plants
RESEARCH ARTICLE

Phylogenetic relationships of Australian Poa (Poaceae: Poinae), including molecular evidence for two new genera, Saxipoa and Sylvipoa

Lynn J. Gillespie A D , Robert J. Soreng B and Surrey W. L. Jacobs C
+ Author Affiliations
- Author Affiliations

A Research Division, Canadian Museum of Nature, PO Box 3443, Station D, Ottawa, Ontario K1P 6P4, Canada.

B Department of Botany, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013-7012, Australia.

C National Herbarium, Royal Botanic Gardens, Sydney, NSW 2000, Australia.

D Corresponding author. Email: lgillespie@mus-nature.ca

Australian Systematic Botany 22(6) 413-436 https://doi.org/10.1071/SB09016
Submitted: 21 April 2009  Accepted: 21 September 2009   Published: 21 December 2009

Abstract

Phylogenetic relationships among Australian species of Poa and other subtribe Poinae genera were studied on the basis of plastid trnT–trnL–trnF and nuclear ribosomal ITS and ETS DNA sequence data. Molecular evidence is provided for two new monotypic endemic Australian genera, Sylvipoa and Saxipoa, on the basis of two species formerly included in Poa, P. queenslandica and P. saxicola, respectively. Both new genera resolved in a clade with three subtribe Poinae genera, the Australian genus Hookerochloa, the South American genus Nicoraepoa, and the arctic genus Arctagrostis. Sylvipoa and Nicoraepoa are sister taxa. Saxipoa resolved as sister to these plus Arctagrostis, but also shares DNA sequence characters with Hookerochloa, suggesting a possible hybrid origin. All other Australian Poa species studied resolved in a subclade within the P. subgenus Poa supersection Homalopoa clade, supporting their classification together in an expanded P. section Brizoides. Five New Zealand and one New Guinea species also resolved in this subclade, supporting their membership in this section. We postulate a minimum of two dispersal events into Australia, one for Poa and one for other Poinae genera, and a minimum of three into New Zealand and two into New Guinea for Poa.


Acknowledgements

We gratefully acknowledge the support and assistance in the field in Australia from Bryan Simon and Paul Peterson, and the following people and institutions for contribution of samples: Susan Aiken, Annie Archambault, Christian Brochmann, Pilar Catalán, Daniel Stančík, Françiose Hennion (French Polar Institute (IPEV) Program no. 136, headed by Marc Lebouvier), Kelvin Lloyd, Terry Macfarlane, Marina Olonova, Paul Peterson, Sierra Stoneberg-Holt, Neville Walsh, Jun Wen, Stoney Wright, and the USDA Plant Introduction Station of Pullman Washington; Richard Gardner, Jeanette Keeling, Peter de Lange, Shane Wright and Ewen Cameron at the University of Auckland (A New Zealand biodiversity database, unpubl.) are acknowledged for their ITS sequences of New Zealand species and voucher information. We thank Michel Paradis and Roger Bull for assistance in sequencing and laboratory support at the Canadian Museum of Nature; and Jeff Saarela for his helpful review of the manuscript. The Canadian Museum of Nature is acknowledged for financial assistance and support of L. J. G., and the Smithsonian Institution for their continued support of R. J. S.


References


Barkworth ME , Capels KM , Long SL , Anderton LK , Piep MB (Eds) (2007) ‘Magnoliophyta: Commelinideae (in part): Poaceae, part 1. Flora of North America North of Mexico. Vol. 24.’ (Oxford University Press: New York)

Bor NL (1952) The genus Poa Linn. in India. Part I. Journal of the Bombay Natural History Society 50, 1–838. [Accessed March 2009].

Hair JB (1968) Contributions to a chromosome atlas of the New Zealand. New Zealand Journal of Botany 6, 267–276. [First available in 2000, but continuously updated. The most recent version was used in this study].

Soreng RJ , Giussani LM , Negritto M (2003) Poa L. In ‘Catalogue of New World grasses (Poaceae): IV. Subfamily Pooideae’. (Eds RJ Soreng, PM Peterson, G Davidse, EJ Judziewicz, FO Zuloaga, TS Filgueiras, O Morrone) pp. 505−580. Contributions from the United States National Herbarium 48, 1–730.

Soreng RJ, Davis JI, Voionmaa MA (2007) A phylogenetic analysis of Poaceae tribe Poeae sensu lato based on morphological characters and sequence data from three plastid-encoded genes: evidence for reticulation, and a new classification for the tribe. Kew Bulletin 62, 425–454. [Accessed September 2009].

Tzvelev NN (1976) ‘Zlaki SSSR.’ (Nauka Publishers: Leningrad). ‘Grasses of the Soviet Union. Vols 1 and 2.’ (1983) (Amerind Publishing Co.: New Delhi, India) [English translation].

Veldkamp JE (1994) Poa L. (Gramineae) in Malesia. Blumea 38, 409–457. open url image1

Vickery JW (1963) Dryopoa, a new grass genus allied to Poa. Contributions from the New South Wales National Herbarium 3, 195–197. open url image1

Vickery JW (1970) A taxonomic study of the genus Poa L. in Australia. Contributions from the New South Wales National Herbarium 4, 145–243. open url image1

Walsh NG (1991) New taxa in Victorian Poaceae. Muelleria 7, 379–387. open url image1

Walsh NG , Weiller CM , Thompson IR (2009) Poa L. In ‘Flora of Australia. Vol. 44A. Poaceae 2’. (Eds Flora Australia Committee) pp. 301–338. (ABRS/CSIRO: Melbourne, Australia)

Zhu G-H , Lui L , Soreng RJ , Olonova MV (2006) Poa L. In ‘Flora of China. Vol. 22. Poaceae’. (Eds Flora of China Editorial Committee) pp. 257−309. (Missouri Botanical Garden Press: St Louis, MO)









Deceased.




Appendix 1.  Collections examined for plastid TLF and nrDNA ITS and ETS, with chromosome numberA (where known for species), infrageneric classification within Poa, country of origin, voucher information and GenBank accession numbers
GenBank numbers in bold indicate new sequences submitted for the present paper; all other sequences are from Gillespie et al. (2007, 2008, in press), except for those downloaded from GenBank, which are indicated by ‘GB’, followed by the literature reference where first published or by the authors who submitted the sequence(s) and, where known, by the voucher information. Incomplete TLF sequences are indicated under ‘TLF GenBank’ as TLL = trnT–trnL spacer and trnL intron, or LLF = trnL intron and trnL–trnF spacer. Herbarium acronyms follow Thiers (continuously updated). Under ‘Country of origin’: ACT = Australian Capital Territory; NSW = New South Wales; WA = Western Australia
Click to zoom