Approved Conservation Advice for Baloskion Longipes
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The Smut Fungi (Ustilaginomycetes) of Restionaceae S. Lat
MYCOLOGIA BALCANICA 3: 19–46 (2006) 19 Th e smut fungi (Ustilaginomycetes) of Restionaceae s. lat. Kálmán Vánky Herbarium Ustilaginales Vánky (H.U.V.), Gabriel-Biel-Str. 5, D-72076 Tübingen, Germany (e-mail: [email protected]) Received 2 October 2005 / Accepted 25 October 2005 Abstract. Smut fungi of Restionaceae s. lat. were studied. Th ey are classifi ed into two genera, Restiosporium and Websdanea. Problems of species delimitation in these smuts are discussed. In addition to the nine known smut fungi, thirteen new species are described and illustrated: Restiosporium anarthriae, R. apodasmiae, R. chaetanthi, R. desmocladii, R. eurychordae, R. fl exuosum, R. hypolaenae, R. lepyrodiae, R. pallentis, R. patei, R. proliferum, R. spathacei, and R. sphacelatum. Key words: new species, Restionaceae s. lat., Restiosporium, smut fungi, taxonomy, Websdanea Introduction and stained in 1 % aqueous uranyl acetate for 1 h in the dark. After fi ve washes in distilled water, the material was Th e monocotyledonous Restionaceae is a remarkable family dehydrated in acetone series, embedded in Spurr’s plastic, of Southern Hemisphere, evergreen, rush-like plants. Th ey and sectioned with a diamond knife. Semi-thin sections are concentrated mainly in SW Africa and in SW Australia. were stained with new fuchsin and crystal violet, mounted Th e c. 320 species of African Restionaceae, in 19 genera, were in ‘Entellan’ and studied in a light microscope. revised by Linder (1985, 1991). Th e 170 species of Australian Spore ball and spore morphology was studied using Restionaceae s. lat. were published by Meney & Pate (1999) a light microscope (LM) with an oil immersion lens at a in a beautifully illustrated monograph. -
GENOME EVOLUTION in MONOCOTS a Dissertation
GENOME EVOLUTION IN MONOCOTS A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Kate L. Hertweck Dr. J. Chris Pires, Dissertation Advisor JULY 2011 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled GENOME EVOLUTION IN MONOCOTS Presented by Kate L. Hertweck A candidate for the degree of Doctor of Philosophy And hereby certify that, in their opinion, it is worthy of acceptance. Dr. J. Chris Pires Dr. Lori Eggert Dr. Candace Galen Dr. Rose‐Marie Muzika ACKNOWLEDGEMENTS I am indebted to many people for their assistance during the course of my graduate education. I would not have derived such a keen understanding of the learning process without the tutelage of Dr. Sandi Abell. Members of the Pires lab provided prolific support in improving lab techniques, computational analysis, greenhouse maintenance, and writing support. Team Monocot, including Dr. Mike Kinney, Dr. Roxi Steele, and Erica Wheeler were particularly helpful, but other lab members working on Brassicaceae (Dr. Zhiyong Xiong, Dr. Maqsood Rehman, Pat Edger, Tatiana Arias, Dustin Mayfield) all provided vital support as well. I am also grateful for the support of a high school student, Cady Anderson, and an undergraduate, Tori Docktor, for their assistance in laboratory procedures. Many people, scientist and otherwise, helped with field collections: Dr. Travis Columbus, Hester Bell, Doug and Judy McGoon, Julie Ketner, Katy Klymus, and William Alexander. Many thanks to Barb Sonderman for taking care of my greenhouse collection of many odd plants brought back from the field. -
The Vegetation of the Western Blue Mountains Including the Capertee, Coxs, Jenolan & Gurnang Areas
Department of Environment and Conservation (NSW) The Vegetation of the Western Blue Mountains including the Capertee, Coxs, Jenolan & Gurnang Areas Volume 1: Technical Report Hawkesbury-Nepean CMA CATCHMENT MANAGEMENT AUTHORITY The Vegetation of the Western Blue Mountains (including the Capertee, Cox’s, Jenolan and Gurnang Areas) Volume 1: Technical Report (Final V1.1) Project funded by the Hawkesbury – Nepean Catchment Management Authority Information and Assessment Section Metropolitan Branch Environmental Protection and Regulation Division Department of Environment and Conservation July 2006 ACKNOWLEDGMENTS This project has been completed by the Special thanks to: Information and Assessment Section, Metropolitan Branch. The numerous land owners including State Forests of NSW who allowed access to their Section Head, Information and Assessment properties. Julie Ravallion The Department of Natural Resources, Forests NSW and Hawkesbury – Nepean CMA for Coordinator, Bioregional Data Group comments on early drafts. Daniel Connolly This report should be referenced as follows: Vegetation Project Officer DEC (2006) The Vegetation of the Western Blue Mountains. Unpublished report funded by Greg Steenbeeke the Hawkesbury – Nepean Catchment Management Authority. Department of GIS, Data Management and Database Environment and Conservation, Hurstville. Coordination Peter Ewin Photos Kylie Madden Vegetation community profile photographs by Greg Steenbeeke Greg Steenbeeke unless otherwise noted. Feature cover photo by Greg Steenbeeke. All Logistics -
Vicariance, Climate Change, Anatomy and Phylogeny of Restionaceae
Botanical Journal of the Linnean Society (2000), 134: 159–177. With 12 figures doi:10.1006/bojl.2000.0368, available online at http://www.idealibrary.com on Under the microscope: plant anatomy and systematics. Edited by P. J. Rudall and P. Gasson Vicariance, climate change, anatomy and phylogeny of Restionaceae H. P. LINDER FLS Bolus Herbarium, University of Cape Town, Rondebosch 7701, South Africa Cutler suggested almost 30 years ago that there was convergent evolution between African and Australian Restionaceae in the distinctive culm anatomical features of Restionaceae. This was based on his interpretation of the homologies of the anatomical features, and these are here tested against a ‘supertree’ phylogeny, based on three separate phylogenies. The first is based on morphology and includes all genera; the other two are based on molecular sequences from the chloroplast genome; one covers the African genera, and the other the Australian genera. This analysis corroborates Cutler’s interpretation of convergent evolution between African and Australian Restionaceae. However, it indicates that for the Australian genera, the evolutionary pathway of the culm anatomy is much more complex than originally thought. In the most likely scenario, the ancestral Restionaceae have protective cells derived from the chlorenchyma. These persist in African Restionaceae, but are soon lost in Australian Restionaceae. Pillar cells and sclerenchyma ribs evolve early in the diversification of Australian Restionaceae, but are secondarily lost numerous times. In some of the reduction cases, the result is a very simple culm anatomy, which Cutler had interpreted as a primitively simple culm type, while in other cases it appears as if the functions of the ribs and pillars may have been taken over by a new structure, protective cells developed from epidermal, rather than chlorenchyma, cells. -
New Combinations Arising from a New Classification of Non-African
21 New combinations arising from a new classification of non-African Restionaceae Barbara G. Briggs and L.A.S. Johnson† Abstract Briggs, Barbara G. and Johnson, L.A.S. (Royal Botanic Gardens, Mrs Macquaries Road, Sydney, NSW 2000, Australia) 1998. New combinations arising from a new classification of non-African Restionaceae. Telopea 8(1): 21–33. New combinations are made in accord with a new, broadly based classification of extra- African Restionaceae. These involve 39 Australian species, of which two extend to New Guinea and the Aru Islands, and one species in each of south-east Asia, New Zealand and Chile. The name Baloskion Raf. is adopted for eight eastern Australian species excluded from Restio Rottb. and Desmocladus Nees is adopted for a group of Western Australian species mostly transferred from Loxocarya R. Br. The previously monotypic genera Meeboldina Suesseng. and Sporadanthus F. Muell. are enlarged. Most other changes involve newly described genera. Four combinations replace illegitimate epithets, two new combinations are made at subspecific rank, and lectotypes are selected for 18 taxa. Introduction A new classification of the genera and species of Australian Restionaceae has been developed through study of exomorphology, anatomy, pollen, seed ornamentation, and flavonoids, with associated DNA sequence studies in progress. The classification is outlined by Briggs and Johnson (1999) and Linder, Briggs and Johnson (1998). It has led to the recognition of 16 new genera (Briggs & Johnson 1998) and has shown that the species hitherto included in some of the genera are unnatural assemblages of taxa. The largest group of inappropriately placed species have until now been referred to Restio Rottb. -
Effects of a Fire Response Trait on Diversification in Replicated Radiations
ORIGINAL ARTICLE doi:10.1111/evo.12273 EFFECTS OF A FIRE RESPONSE TRAIT ON DIVERSIFICATION IN REPLICATED RADIATIONS Glenn Litsios,1,2 Rafael O. Wuest,¨ 3 Anna Kostikova,1,2 Felix´ Forest,4 Christian Lexer,5 H. Peter Linder,6 Peter B. Pearman,3 Niklaus E. Zimmermann,3 and Nicolas Salamin1,2,7 1Department of Ecology and Evolution, Biophore, University of Lausanne, CH-1015 Lausanne, Switzerland 2Swiss Institute of Bioinformatics, Quartier Sorge, CH-1015 Lausanne, Switzerland 3Landscape Dynamics, Swiss Federal Research Institute WSL, CH-8903 Birmensdorf, Switzerland 4Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3DS, United Kingdom 5Unit of Ecology and Evolution, Department of Biology, University of Fribourg, Chemin du Musee´ 10, CH-1700 Fribourg, Switzerland 6Insitute for Systematic Botany, University of Zurich, 8008 Zurich, Switzerland 7E-mail: [email protected] Received May 14, 2013 Accepted September 9, 2013 Fire has been proposed as a factor explaining the exceptional plant species richness found in Mediterranean regions. A fire response trait that allows plants to cope with frequent fire by either reseeding or resprouting could differentially affect rates of species diversification. However, little is known about the generality of the effects of differing fire response on species evolution. We study this question in the Restionaceae, a family that radiated in Southern Africa and Australia. These radiations occurred independently and represent evolutionary replicates. We apply Bayesian approaches to estimate trait-specific diversification rates and patterns of climatic niche evolution. We also compare the climatic heterogeneity of South Africa and Australia. Reseeders diversify faster than resprouters in South Africa, but not in Australia. -
Nuclear Genes, Matk and the Phylogeny of the Poales
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2018 Nuclear genes, matK and the phylogeny of the Poales Hochbach, Anne ; Linder, H Peter ; Röser, Martin Abstract: Phylogenetic relationships within the monocot order Poales have been well studied, but sev- eral unrelated questions remain. These include the relationships among the basal families in the order, family delimitations within the restiid clade, and the search for nuclear single-copy gene loci to test the relationships based on chloroplast loci. To this end two nuclear loci (PhyB, Topo6) were explored both at the ordinal level, and within the Bromeliaceae and the restiid clade. First, a plastid reference tree was inferred based on matK, using 140 taxa covering all APG IV families of Poales, and analyzed using parsimony, maximum likelihood and Bayesian methods. The trees inferred from matK closely approach the published phylogeny based on whole-plastome sequencing. Of the two nuclear loci, Topo6 supported a congruent, but much less resolved phylogeny. By contrast, PhyB indicated different phylo- genetic relationships, with, inter alia, Mayacaceae and Typhaceae sister to Poaceae, and Flagellariaceae in a basally branching position within the Poales. Within the restiid clade the differences between the three markers appear less serious. The Anarthria clade is first diverging in all analyses, followed by Restionoideae, Sporadanthoideae, Centrolepidoideae and Leptocarpoideae in the matK and Topo6 data, but in the PhyB data Centrolepidoideae diverges next, followed by a paraphyletic Restionoideae with a clade consisting of the monophyletic Sporadanthoideae and Leptocarpoideae nested within them. The Bromeliaceae phylogeny obtained from Topo6 is insufficiently sampled to make reliable statements, but indicates a good starting point for further investigations. -
New Genera and Species of Australian Restionaceae (Poales)
345 New genera and species of Australian Restionaceae (Poales) Barbara G. Briggs and L.A.S. Johnson† Abstract Briggs, Barbara G. and Johnson, L.A.S. (Royal Botanic Gardens, Mrs Macquaries Road, Sydney, NSW 2000, Australia) 1998. New genera and species of Australian Restionaceae (Poales). Telopea 7(4): 345–373. Sixteen new genera and five new species of Australian Restionaceae are described and combinations made for a further eleven species. Newly described genera are Catacolea, Kulinia, Guringalia, Acion, Saropsis, Chordifex, Eurychorda, Platychorda, Tremulina, Melanostachya, Taraxis, Tyrbastes, Cytogonidium, Stenotalis, Dapsilanthus, Apodasmia. Newly described type species are: Catacolea enodis, Kulinia eludens, Chordifex stenandrus, Taraxis grossa, Tyrbastes glaucescens. New combinations are made for the type species of the remaining genera: Guringalia dimorpha, Acion monocephalum, Saropsis fastigiata, Eurychorda complanata, Platychorda applanata, Tremulina tremula, Melanostachya ustulata, Cytogonidium leptocarpoides, Stenotalis ramosissima, Dapsilanthus elatior, Apodasmia brownii. Lectotypes are selected for several species. Brief comment is included on culm anatomy, flavonoids, seed ornamentation and DNA findings, in addition to exomorphological features. Keys are provided to distinguish the new genera from other members of the Desmocladus, Loxocarya and Leptocarpus groups. All the new genera occur in Australia but Apodasmia also includes species in New Zealand and Chile while Dapsilanthus is represented also in New Guinea, Aru Islands and Southeast Asia. Introduction The last comprehensive systematic account of Australian Restionaceae was by Bentham (1878), building especially on the notable work of Brown (1810) and Mueller (1872–4). Subsequently 12 relevant new genera have been described, but two of these, Desmocladus Nees and Baloskion Raf., were never adopted by botanists in Australia and one, Sporadanthus F. -
Tracing the Past, Conserving the Future the British and Irish Botanical Expedition to Tasmania 2018
Tracing the Past, Conserving the Future The British and Irish Botanical Expedition to Tasmania 2018 Piers Lunt Merlin 716 © Piers Lunt, April 2018 All photographic and graphical materials by the author, unless otherwise stated. Cover photo: Waratah (Telopea truncata), floral emblem of Tasmania. Near Pine Lake, Central Plateau Conservation Area, Tasmania, January 2018. 2 Tracing the Past, Conserving the Future The British and Irish Botanical Expedition to Tasmania 2018 3 4 CONTENTS Acknowledgments..................................................................................................................................7 Introduction...........................................................................................................................................9 Part One: Background..........................................................................................................................15 The Island.................................................................................................................................19 Harold Comber.........................................................................................................................21 Woods of the World................................................................................................................23 Part Two: The Expedition.....................................................................................................................25 Departure.................................................................................................................................27 -
Restionaceae (Poales) in the Footsteps of Robert Brown
499 Restionaceae (Poales) in the footsteps of Robert Brown Barbara G. Briggs Abstract Barbara G. Briggs (National Herbarium of New South Wales, Mrs Macquaries Road, Sydney 2000, Australia; [email protected].) 2004. Restionaceae (Poales) in the footsteps of Robert Brown. Telopea 10(2): 499–503. Brown visited major centres of restiad diversity in Africa at the Cape of Good Hope and in Western Australia at King Georges Sound and Lucky Bay; other taxa were collected in northern and eastern Australia, including Tasmania. He described five genera and 36 species now included in Restionaceae, and four genera and 35 species since excluded from that family. His observation, enlightened by fieldwork, was remarkable and some species he named are now recognised again after decades in confusion or synonymy. Mostly he correctly matched dioecious males and females, but for one species these were placed in different genera. Restionaceae has been much cut down in size since Brown’s time. In the Prodromus, Restiaceae included what are now Anarthriaceae, Centrolepidaceae, Eriocaulaceae and Xyridaceae, as well as Lyginiaceae if this and Hopkinsiaceae are recognised as separate from Anarthriaceae sens. strict. Currently 145 Australian Restionaceae species are recognised, in 31 genera. The 24 species that Brown included in Restio (22 of them then newly described) are now distributed among 11 genera, the majority in Chordifex, Baloskion and Hypolaena, while Restio is restricted to African and Madagascan species. Anatomy, palynology and especially DNA sequencing have clarified relationships within Restionaceae and between families of Poales. Molecular data indicate that Centrolepidaceae forms the sister-group to Restionaceae, unless it is embedded in the latter. -
Wallum and Related Vegetation on the NSW North Coast: Description and Phytosociological Analysis
202 Cunninghamia 8(2): 2003 Griffith et al., Wallum vegetation on NSW North Coast Wallum and related vegetation on the NSW North Coast: description and phytosociological analysis S. J. Griffith1, C. Bale1, P. Adam2 and R. Wilson3 1Centre for Ecology, Evolution and Systematics, University of New England, Armidale, NSW, AUSTRALIA 2351, 2School of Biological, Earth and Environmental Sciences, University of New South Wales, Sydney, NSW, AUSTRALIA 2052, 315/137 Jabanungga Avenue, Ngunnawal, ACT, AUSTRALIA 2913. Abstract: Wallum is the regionally distinct vegetation on coastal dunefields, beach ridge plains and sandy backbarrier flats in subtropical northern NSW and southern Queensland (22°S to 33°S). This study examined floristic patterns in the wallum and allied vegetation along 400 km of coastline in north-eastern NSW. Floristic and environmental data were compiled for 494 quadrats allocated on the basis of air photo pattern and latitude. A phytosociological classification displayed strong congruence with an initial classification based upon photo pattern, especially for single stratum vegetation, thereby suggesting that API (air photo interpretation) is a valuable technique for the recognition of floristic assemblages. The utility of API for depicting the spatial distribution of tallest stratum species in multi-stratum vegetation was also confirmed. Nonetheless, photo signatures of the tallest stratum are less satisfactory as surrogates for identifying noda for the full complement of species in multi-stratum vegetation. Ordination supported the numerical classification, and reinforced the value of API for capturing meaningful biological and environmental data. Plant – environment relationships were examined for a range of variables. The consistent trend to emerge was a comparatively strong correlation between floristic composition and topographic position, and in some instances also between floristic composition and geology. -
Senecio Extensus (Subalpine Fireweed) Senecio Extensus
Notesheet for Senecio extensus (subalpine fireweed) Senecio extensus subalpine fireweed T A S M A N I A N T H R E A T E N E D S P E C I E S N O T E S H E E T Image by Mark Wapstra Scientific name: Senecio extensus I.Thomps., Muelleria 19: 150 (2004) Common name: subalpine fireweed Group: vascular plant, dicotyledon, family Asteraceae Status: Threatened Species Protection Act 1995: listing as endangered under consideration Environment Protection and Biodiversity Conservation Act 1999: Not Listed Distribution: Biogeographic origin: not endemic to Tasmania Tasmanian Natural Resource Management regions: South Tasmanian IBRA Bioregions (V6): Central Highlands Figure 1. Distribution of Senecio extensus in Tasmania, Plate 1. Senecio extensus at Top Marshes, 3 Jan. 2020 showing IBRA bioregions (V6) (image by Mark Wapstra) Threatened Species Section – Department of Primary Industries, Parks, Water and Environment Notesheet for Senecio extensus (subalpine fireweed) SUMMARY: Senecio extensus (subalpine recently burnt areas. It is not known whether fireweed) is a perennial herb that was only the species germinates from soil-stored seed. known in Tasmania from a single collection made in 1984 until confirmed in 2020 from two Survey techniques sites on a broad undulating area of dolerite- The peak flowering period of most species of based sedgy plain surrounded by open shrubby Senecio is spring through summer and into subalpine forest at about 1,000 m a.s.l. The two autumn, but the detection window is likely to Tasmanian sites are in one sub-population, the be much wider, although confirmation of total area of occupancy less than 1 ha and the identification usually requires mature achenes total number of mature individuals fewer than (Wapstra et al.