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Breeding System Diversification and Evolution in American Poa Supersect. Homalopoa (Poaceae: Poeae: Poinae)
Annals of Botany Page 1 of 23 doi:10.1093/aob/mcw108, available online at www.aob.oxfordjournals.org Breeding system diversification and evolution in American Poa supersect. Homalopoa (Poaceae: Poeae: Poinae) Liliana M. Giussani1,*, Lynn J. Gillespie2, M. Amalia Scataglini1,Marıa A. Negritto3, Ana M. Anton4 and Robert J. Soreng5 1Instituto de Botanica Darwinion, San Isidro, Buenos Aires, Argentina, 2Research and Collections Division, Canadian Museum of Nature, Ottawa, Ontario, Canada, 3Universidad de Magdalena, Santa Marta, Colombia, 4Instituto Multidisciplinario de Biologıa Vegetal (IMBIV), CONICET-UNC, Cordoba, Argentina and 5Department of Botany, Smithsonian Institution, Washington, DC, USA *For correspondence. E-mail [email protected] Received: 11 December 2015 Returned for revision: 18 February 2016 Accepted: 18 March 2016 Downloaded from Background and Aims Poa subgenus Poa supersect. Homalopoa has diversified extensively in the Americas. Over half of the species in the supersection are diclinous; most of these are from the New World, while a few are from South-East Asia. Diclinism in Homalopoa can be divided into three main types: gynomonoecism, gynodioe- cism and dioecism. Here the sampling of species of New World Homalopoa is expanded to date its origin and diver- sification in North and South America and examine the evolution and origin of the breeding system diversity. Methods A total of 124 specimens were included in the matrix, of which 89 are species of Poa supersect. http://aob.oxfordjournals.org/ Homalopoa sections Acutifoliae, Anthochloa, Brizoides, Dasypoa, Dioicopoa, Dissanthelium, Homalopoa sensu lato (s.l.), Madropoa and Tovarochloa, and the informal Punapoa group. Bayesian and parsimony analyses were conducted on the data sets based on four markers: the nuclear ribosomal internal tanscribed spacer (ITS) and exter- nal transcribed spacer (ETS), and plastid trnT-L and trnL-F. -
Poa Billardierei
Poa billardierei COMMON NAME Sand tussock, hinarepe SYNONYMS Festuca littoralis Labill.; Schedonorus littoralis (Labill.) P.Beauv.; Triodia billardierei Spreng.; Poa billardierei (Spreng.)St.-Yves; Schedonorus billardiereanus Nees; Arundo triodioides Trin.; Schedonorus littoralis var. alpha minor Hook.f.; Austrofestuca littoralis (Labill.) E.B.Alexev. FAMILY Poaceae AUTHORITY Poa billardierei (Spreng.)St.-Yves FLORA CATEGORY Vascular – Native ENDEMIC TAXON No Austrofestuca littoralis. Photographer: Kevin Matthews ENDEMIC GENUS No ENDEMIC FAMILY No STRUCTURAL CLASS Grasses NVS CODE POABIL CHROMOSOME NUMBER 2n = 28 CURRENT CONSERVATION STATUS 2012 | At Risk – Declining | Qualifiers: SO PREVIOUS CONSERVATION STATUSES 2009 | At Risk – Declining | Qualifiers: SO 2004 | Gradual Decline DISTRIBUTION Austrofestuca littoralis. Photographer: Geoff North Island, South Island, Chatham Island (apparently absent from Walls Chatham Island now despite being formerly abundant). Also found in temperate Australia. HABITAT Coastal dunes; sandy and rocky places near the shore, especially foredunes and dune hollows. FEATURES Yellow-green tussocks up to about 70 cm tall. Leaves fine, rolled, somewhat drooping (coarser than silver tussock), initially green, often fading at tips to silver, and drying to golden-straw colour. Seed heads no longer than leaves; seeds relatively large, barley-like, leaving a characteristic zig-zag look to the remaining head when fallen. Flowers in early summer and the seed are produced in late summer. It could be confused with Poa chathamica which has blue- green or grass-green flat leaves and an open seed head which overtops the foliage. It could also be confused with marram grass which has similar foliage but large cat’stail-like seed heads which overtop the foliage. SIMILAR TAXA Ammophila arenaria (marram grass) is often confused with sand tussock because they grow in the same habitat. -
The Vegetation Communities Native Grassland
Edition 2 From Forest to Fjaeldmark The Vegetation Communities Native grassland Themeda australis Edition 2 From Forest to Fjaeldmark (revised - October 2017) 1 Native grassland Community (Code) Page Coastal grass and herbfield (GHC) 5 Highland Poa grassland (GPH) 7 Lowland grassland complex (GCL) 9 Lowland grassy sedgeland (GSL) 11 Lowland Poa labillardierei grassland (GPL) 12 Lowland Themeda triandra grassland (GTL) 14 Rockplate grassland (GRP) 16 General description align the key and the description of Lowland grassland complex ( ) with respect to the Native grasslands are defined as areas of native GCL required cover of native grass species. In 2017 vegetation dominated by native grasses with few or further minor revisions were made to improve no emergent woody species. Different types of information for general management issues, and to native grassland can be found in a variety of habitats, improve the description of Coastal grass and including coastal fore-dunes, dry slopes and valley herbfield (GHC) and its differentiation from Lowland bottoms, rock plates and subalpine flats. The lowland Poa labillardierei grassland (GPL). This is reflected in temperate grassland types have been recognised as the key to this Section. some of the most threatened vegetation communities in Australia. General management issues Some areas of native grassland are human-induced Most lowland native grassland in Tasmania has been and exist as a result of heavy burning, tree clearing cleared for agriculture since European settlement or dieback of the tree layer in grassy woodlands. (Barker 1999, Gilfedder 1990, Kirkpatrick et al. 1988, There are seven grassland communities recognised Kirkpatrick 1991, Williams et al. 2007). -
Trnl–Trnf) Nucleotide Sequences Kelvin M
Aliso: A Journal of Systematic and Evolutionary Botany Volume 23 | Issue 1 Article 32 2007 Phylogeny and Biogeography of Endemic Festuca (Poaceae) from New Zealand Based on Nuclear (ITS) and Chloroplast (trnL–trnF) Nucleotide Sequences Kelvin M. Lloyd Landcare Research, Dunedin, New Zealand Angela M. Hunter University of Otago, Dunedin, New Zealand David A. Orlovich University of Otago, Dunedin, New Zealand Suzanne J. Draffin University of Otago, Dunedin, New Zealand Alan V. Stewart PGG Seeds, Christchurch, New Zealand See next page for additional authors Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons, and the Ecology and Evolutionary Biology Commons Recommended Citation Lloyd, Kelvin M.; Hunter, Angela M.; Orlovich, David A.; Draffin,uza S nne J.; Stewart, Alan V.; and Lee, William G. (2007) "Phylogeny and Biogeography of Endemic Festuca (Poaceae) from New Zealand Based on Nuclear (ITS) and Chloroplast (trnL–trnF) Nucleotide Sequences," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 23: Iss. 1, Article 32. Available at: http://scholarship.claremont.edu/aliso/vol23/iss1/32 Phylogeny and Biogeography of Endemic Festuca (Poaceae) from New Zealand Based on Nuclear (ITS) and Chloroplast (trnL–trnF) Nucleotide Sequences Authors Kelvin M. Lloyd, Angela M. Hunter, David A. Orlovich, Suzanne J. Draffin, Alan V. Stewart, and William G. Lee This article is available in Aliso: A Journal of Systematic and Evolutionary Botany: http://scholarship.claremont.edu/aliso/vol23/iss1/ 32 Aliso 23, pp. 406–419 ᭧ 2007, Rancho Santa Ana Botanic Garden PHYLOGENY AND BIOGEOGRAPHY OF ENDEMIC FESTUCA (POACEAE) FROM NEW ZEALAND BASED ON NUCLEAR (ITS) AND CHLOROPLAST (trnL–trnF) NUCLEOTIDE SEQUENCES KELVIN M. -
Grass Genera of Southern Africa: Interactive Identification and Information Retrieval from an Automated Data Bank
452 S.-Afr.Tydskr. Plantk. , 1989, 55(4): 452-463 Grass genera of southern Africa: Interactive identification and information retrieval from an automated data bank L. Watson*, G.E. Gibbs Russell 1 and M.J. Dallwitz Taxonomy Laboratory, Research School of Biological Sciences, Australian National University, GPO Box 475, A.C.T. 2601, Australia; Botanical Research Institute, Private Bag X1 01, Pretoria, 0001 Republic of South Africa and Division of Entomology, Commonwealth Scientific and Industrial Research Organization, GPO Box 1700, Canberra City, A.C.T. 2601, Australia 1 Present address: Missouri Botanical Garden, P.O. Box 299, St. Louis, Missouri, USA 63166-0299 A new interactive system for computerized taxonomic identification and information retrieval, operable on MS DOS microcomputers, is now available. In this application to southern African grass genera the data include synonyms, morphology, anatomy, physiology, cytology, classification, pathogens, world and local distribu tions and references. The program is part of the DELTA system, which also provides natural language descriptions and printed keys. The data for the southern African genera can be provided separately, or inclu ded in the complete data for the grass genera of the world. 'n Nuwe interaktiewe stelsel vir gerekenariseerde taksonomiese identifisering en inligtingsherwinning, bedryf baar op MS-DOS-mikrorekenaars, is nou beskikbaar. Hierdie toepassing op Suider-Afrikaanse grasgenusse bevat data oor sinonieme, morfologie, anatomie, fisiologie, sitologie, klassifikasie, patogene, wereldwye en plaaslike verspreidings en verwysings. Die program is deel van die DELTA-stelsel, wat ook voorsiening maak vir beskrywings in gewone taal en gedrukte sleutels. Die data vir die Suider-Afrikaanse genusse kan afsonderlik verskaf word, of by die volledige data vir die grasgenusse van die wereld ingesluit word. -
Phylogeny, Morphology and the Role of Hybridization As Driving Force Of
bioRxiv preprint doi: https://doi.org/10.1101/707588; this version posted July 18, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Phylogeny, morphology and the role of hybridization as driving force of evolution in 2 grass tribes Aveneae and Poeae (Poaceae) 3 4 Natalia Tkach,1 Julia Schneider,1 Elke Döring,1 Alexandra Wölk,1 Anne Hochbach,1 Jana 5 Nissen,1 Grit Winterfeld,1 Solveig Meyer,1 Jennifer Gabriel,1,2 Matthias H. Hoffmann3 & 6 Martin Röser1 7 8 1 Martin Luther University Halle-Wittenberg, Institute of Biology, Geobotany and Botanical 9 Garden, Dept. of Systematic Botany, Neuwerk 21, 06108 Halle, Germany 10 2 Present address: German Centre for Integrative Biodiversity Research (iDiv), Deutscher 11 Platz 5e, 04103 Leipzig, Germany 12 3 Martin Luther University Halle-Wittenberg, Institute of Biology, Geobotany and Botanical 13 Garden, Am Kirchtor 3, 06108 Halle, Germany 14 15 Addresses for correspondence: Martin Röser, [email protected]; Natalia 16 Tkach, [email protected] 17 18 ABSTRACT 19 To investigate the evolutionary diversification and morphological evolution of grass 20 supertribe Poodae (subfam. Pooideae, Poaceae) we conducted a comprehensive molecular 21 phylogenetic analysis including representatives from most of their accepted genera. We 22 focused on generating a DNA sequence dataset of plastid matK gene–3'trnK exon and trnL– 23 trnF regions and nuclear ribosomal ITS1–5.8S gene–ITS2 and ETS that was taxonomically 24 overlapping as completely as possible (altogether 257 species). -
Publications for Murray Henwood 2018 2017 2016 2015 2014 2013
Publications for Murray Henwood 2018 hamptonii, Araliaceae): an enigmatic species with a rich history Plunkett, G., Pimenov, M., Reduron, J., Kljuykov, E., van Wyk, in bioprospecting. Telopea, 18, 297-304. <a B., Ostroumova, T., Henwood, M., Tilney, P., Spalik, K., href="http://dx.doi.org/10.7751/telopea8767">[More Watson, M., Hart, J., et al (2018). Apiaceae. In J. Kadereit, V. Information]</a> Bittrich (Eds.), Flowering Plants. Eudicots: The Families and Kodela, P., Henwood, M. (2015). Lectotypification of Actinotus Genera of Vascular Plants, (pp. 9-206). Cham: Springer, Cham. paddisonii R.T.Baker (Apiaceae: Mackinlayoideae). Telopea, <a href="http://dx.doi.org/10.1007/978-3-319-93605- 18, 57-60. <a 5_2">[More Information]</a> href="http://dx.doi.org/10.7751/telopea8465">[More Plunkett, G., Wen, J., Lowry II, P., Mitchell, A., Henwood, M., Information]</a> Fiaschi, P. (2018). Araliaceae. In J. Kadereit, V. Bittrich (Eds.), Wilson, T., Elkan, L., Henwood, M., Murray, L., Renner, M., Flowering Plants. Eudicots: The Families and Genera of Wardrop, C. (2015). Prostanthera conniana (Lamiaceae, Vascular Plants, (pp. 413-446). Cham: Springer, Cham. <a Westringieae), a new species from the Southern Tablelands, href="http://dx.doi.org/10.1007/978-3-319-93605-5_4">[More New South Wales, Australia. Telopea, 18, 519-526. <a Information]</a> href="http://dx.doi.org/10.7751/telopea10042">[More Foster, C., Henwood, M., Ho, S. (2018). Plastome sequences Information]</a> and exploration of tree-space help to resolve the phylogeny of Gibbons, K., Conn, B., Henwood, M. (2015). Status of names riceflowers (Thymelaeaceae: Pimelea). Molecular of Mitrasacme species occurring outside Australia. -
Breeding System Diversification and Evolution in American Poa Supersect
Annals of Botany 118: 281–303, 2016 doi:10.1093/aob/mcw108, available online at www.aob.oxfordjournals.org Breeding system diversification and evolution in American Poa supersect. Homalopoa (Poaceae: Poeae: Poinae) Liliana M. Giussani1,*, Lynn J. Gillespie2, M. Amalia Scataglini1,Marıa A. Negritto3, Ana M. Anton4 and Robert J. Soreng5 1Instituto de Botanica Darwinion, San Isidro, Buenos Aires, Argentina, 2Research and Collections Division, Canadian Museum of Nature, Ottawa, Ontario, Canada, 3Universidad de Magdalena, Santa Marta, Colombia, 4Instituto Multidisciplinario de Biologıa Vegetal (IMBIV), CONICET-UNC, Cordoba, Argentina and 5Department of Botany, Smithsonian Institution, Washington, DC, USA *For correspondence. E-mail [email protected] Received: 11 December 2015 Returned for revision: 18 February 2016 Accepted: 18 March 2016 Published electronically: 3 July 2016 Background and Aims Poa subgenus Poa supersect. Homalopoa has diversified extensively in the Americas. Over half of the species in the supersection are diclinous; most of these are from the New World, while a few are from South-East Asia. Diclinism in Homalopoa can be divided into three main types: gynomonoecism, gynodioe- cism and dioecism. Here the sampling of species of New World Homalopoa is expanded to date its origin and diver- sification in North and South America and examine the evolution and origin of the breeding system diversity. Methods A total of 124 specimens were included in the matrix, of which 89 are species of Poa supersect. Homalopoa sections Acutifoliae, Anthochloa, Brizoides, Dasypoa, Dioicopoa, Dissanthelium, Homalopoa sensu lato (s.l.), Madropoa and Tovarochloa, and the informal Punapoa group. Bayesian and parsimony analyses were conducted on the data sets based on four markers: the nuclear ribosomal internal tanscribed spacer (ITS) and exter- nal transcribed spacer (ETS), and plastid trnT-L and trnL-F. -
Based on Nrits, ETS, and Trntlf Data
running head: Gillespie et al.: phylogeny and reticulation in poi- nae d i v e r s i t y , p h y l o g e n y , a n d e v o l u t i o n i n t h e monocotyledons e d i t e d b y s e b e r g , p e t e r s e n , b a r f o d & d a v i s a a r h u s u n i v e r s i t y p r e s s , d e n m a r k , 2 0 1 0 Phylogeny and Reticulation in Subtribe Poinae and Related Subtribes (Poaceae) Based on nrITS, ETS, and trnTLF data Lynn J. Gillespie,1 Robert J. Soreng,2 Michel Paradis,1 and Roger D. Bull1 1Canadian Museum of Nature, Research Division, P.O. Box 3443, Station D. Ottawa, ON, K1P 6P4, Canada 2Smithsonian Institution, Department of Botany MRC-166, National Museum of Natural History, Washington, District of Columbia 20013-7012 U.S.A. Author for correspondence ([email protected]) Abstract—The worldwide temperate to arctic distributed subtribe Poinae com- prises the largest grass genus Poa (500+ species) and 14 smaller genera. Phyloge- netic analyses of combined nuclear ribosomal ITS and ETS and chloroplast trnT- trnL-trnF sequence data for Poinae and the closely related subtribes Alopecurinae, Cinninae, Miliinae, and Puccinelliinae resolve three strongly supported major clades: 1) Poa; 2) all Poinae taxa except Poa, and including Alopecurus, Beckmannia (both Alopecurinae), and Cinna; and 3) subtribe Puccinelliinae. -
Stenostachys Enysii
Stenostachys enysii SYNONYMS Agropyron enysii Kirk, Elymus enysii (Kirk) Á.Löve et Connor, Asprella aristata Petrie, Agropyron aristatum Cheeseman; Australopyrum enysii (Kirk) Connor FAMILY Poaceae AUTHORITY Stenostachys enysii (Kirk) Barkworth et S.W.L.Jacobs FLORA CATEGORY Vascular – Native ENDEMIC TAXON Yes ENDEMIC GENUS No ENDEMIC FAMILY No STRUCTURAL CLASS Grasses NVS CODE AGRARI CHROMOSOME NUMBER 2n = 28 CURRENT CONSERVATION STATUS Australopyrum enysii. Photographer: Alan 2012 | At Risk – Naturally Uncommon | Qualifiers: DP, Sp Stewart PREVIOUS CONSERVATION STATUSES 2009 | At Risk – Naturally Uncommon 2004 | Not Threatened DISTRIBUTION Endemic. South Island only Nelson, then east of the main divide from Marlborough to Canterbury HABITAT Montane, subalpine to alpine (up to 1800 m a.s.l.), usually in shaded sites such as in and around boulders under rock overhangs, or in low scrub. Also in flushes within tussock grassland FEATURES Tufted, bronze-coloured, flat-leaved grass. Culm slender, drooping, inflorescence often hidden in foliage. Leaf sheath 60-80 mm, covered in long hairs, these retrorse, erect or pubescent. Ligule 0.5-0.75 mm. Leaf-blade 200 x 2-4 mm, flat, soft, upper surface densely retrorse hairy or glabrous, undersides antrorsely prickle-toothed, margin prickle-toothed. Culm 250-800 mm. Inflorescence 50-130 mm, with 10-18 compact spikelets. Spikelets 10-16 mm, shining. Glumes abut equal, narrow 6-9 mm, 1-3-nerved, scabrid, becoming awn-like, margin prickle-toothed. Lemma 7-10 mm, > palea, glaucous, apex bifid, awn 1-3.5 mm, indented at base. Palea 6-9 mm, apex bifid. Rachilla 1-2 mm flared near apex. Callus 0.25 mm blunt, surrounded by minute hairs. -
Publications by Surrey Jacobs: 1946–2009 (In Chronological Order) Anderson DJ, Jacobs SWL & Malik AR (1969) Studies on Structure in Plant Communities VI
Telopea 13(1–2): 2011 1 Publications by Surrey Jacobs: 1946–2009 (in chronological order) Anderson DJ, Jacobs SWL & Malik AR (1969) Studies on structure in plant communities VI. The significance of pattern evaluation in some Australian dry-land vegetation types. Australian Journal of Botany 17: 315–322. Jacobs SWL (1971) Systematic position of the genera Triodia R.Br. and Plectrachne Henr. (Gramineae). Proceedings of the Linnean Society of New South Wales 96 (3): 175–185. Jacobs SWL (1973) Practical plant ecology: principles of measurement and sampling. Science Bulletin 18: 47–48. Carolin RC, Jacobs SWL & Vesk M (1973) The structure of the cells of the mesophyll and parenchymatous bundle sheath of the Gramineae. Botanical Journal of the Linnean Society 66: 259–275. Jacobs SWL (1974) Ecological studies on the genera Triodia R.Br. and Plectrachne Henr. in Australia. Ph.D. thesis, University of Sydney. Carolin RC, Jacobs SWL & Vesk M (1975) Leaf structure in Chenopodiaceae. Botanische Jahrbücher für Systematik 95: 226–255. Carolin RC, Jacobs SWL & Vesk M (1977) The ultrastructure of Kranz Cells in the family Cyperaceae. Botanical Gazette 138: 413–419. Carolin RC, Jacobs SWL & Vesk M (1978) Kranz cells and mesophyll in the Chenopodiales. Australian Journal of Botany 26: 683–698. Jacobs SWL & Chapman EA (1979) Photosynthetic responses in semi-arid environments. Pp. 41–53 in Graetz RD & Howes KMW (eds) Studies of the Australian Arid Zone. IV. Chenopod Shrublands. Proceedings of a Symposium held by the Rangelands Research Unit of the Division of Land Resources Management.(CSIRO, Melbourne) Raison JK, Chapman EA, Wright LC & Jacobs SWL (1979) Membrane lipid transitions: their correlation with the climatic distribution of plants. -
Brachypodium, Taxonomy It, Only The
BLUMEA 34 (1989) 61-76 Australopyrum, Brachypodium, and Elymus (Gramineae) in Malesia J.F. Veldkamp & H.J. van Scheindelen Rijksherbarium, Leiden, The Netherlands Summary Brachypodium sylvaticum (Huds.) Beauv. has 1 species and 2 varieties in Malesia. Brachypo- The Australian dium longisetum Hitchc. is transferred to Elymus. genus Australopyrum (Tsvel.) Löve (Gramineae-Triticeae) is represented by a new species in New Guinea. The species is curious for thin the end of the inflorescence which is among grasses not only having a seta at rachis, unique the but because of the uncinate the and lemmas. Lateral among Pooideae, especially awn on glumes transfer between families be The latter tribe and genetic may present. two taxa represent a (Triticeae) thus far recorded for the Gramineae of Malesia. genera not indigenous Introduction Taxonomy Brachypodium Beauv. is a small genus of about 17 species. There is no recent revision of local the for it, only some ones, e.g. posthumous one Europe by Saint- Yves (1934), and the one by Honda (1937) for Japan, Taiwan, and Manchuria, who both distinguished a host of taxa in an unwieldy system. Tateoka has published vari- ous notes on the genus, the most important of which is his summary in 1968. The genusappears at present to be most variable in the Iberean Peninsula (Schippmann, 1986), but this may well be a secondary centre of diversification: it extends far into Asia with one curious endemic in Taiwan and one species, B. sylvaticum (Huds.) Beauv., with two varieties in the mountains of most of Malesia. The New Guinea endemic, B. longisetum Hitchc., will be discussed later.