Phyllocladus Alpinus
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JUDD W.S. Et. Al. (2002) Plant Systematics: a Phylogenetic Approach. Chapter 7. an Overview of Green
UNCORRECTED PAGE PROOFS An Overview of Green Plant Phylogeny he word plant is commonly used to refer to any auto- trophic eukaryotic organism capable of converting light energy into chemical energy via the process of photosynthe- sis. More specifically, these organisms produce carbohydrates from carbon dioxide and water in the presence of chlorophyll inside of organelles called chloroplasts. Sometimes the term plant is extended to include autotrophic prokaryotic forms, especially the (eu)bacterial lineage known as the cyanobacteria (or blue- green algae). Many traditional botany textbooks even include the fungi, which differ dramatically in being heterotrophic eukaryotic organisms that enzymatically break down living or dead organic material and then absorb the simpler products. Fungi appear to be more closely related to animals, another lineage of heterotrophs characterized by eating other organisms and digesting them inter- nally. In this chapter we first briefly discuss the origin and evolution of several separately evolved plant lineages, both to acquaint you with these important branches of the tree of life and to help put the green plant lineage in broad phylogenetic perspective. We then focus attention on the evolution of green plants, emphasizing sev- eral critical transitions. Specifically, we concentrate on the origins of land plants (embryophytes), of vascular plants (tracheophytes), of 1 UNCORRECTED PAGE PROOFS 2 CHAPTER SEVEN seed plants (spermatophytes), and of flowering plants dons.” In some cases it is possible to abandon such (angiosperms). names entirely, but in others it is tempting to retain Although knowledge of fossil plants is critical to a them, either as common names for certain forms of orga- deep understanding of each of these shifts and some key nization (e.g., the “bryophytic” life cycle), or to refer to a fossils are mentioned, much of our discussion focuses on clade (e.g., applying “gymnosperms” to a hypothesized extant groups. -
Pollination Drop in Relation to Cone Morphology in Podocarpaceae: a Novel Reproductive Mechanism Author(S): P
Pollination Drop in Relation to Cone Morphology in Podocarpaceae: A Novel Reproductive Mechanism Author(s): P. B. Tomlinson, J. E. Braggins, J. A. Rattenbury Source: American Journal of Botany, Vol. 78, No. 9 (Sep., 1991), pp. 1289-1303 Published by: Botanical Society of America Stable URL: http://www.jstor.org/stable/2444932 . Accessed: 23/08/2011 15:47 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. Botanical Society of America is collaborating with JSTOR to digitize, preserve and extend access to American Journal of Botany. http://www.jstor.org AmericanJournal of Botany 78(9): 1289-1303. 1991. POLLINATION DROP IN RELATION TO CONE MORPHOLOGY IN PODOCARPACEAE: A NOVEL REPRODUCTIVE MECHANISM' P. B. TOMLINSON,2'4 J. E. BRAGGINS,3 AND J. A. RATTENBURY3 2HarvardForest, Petersham, Massachusetts 01366; and 3Departmentof Botany, University of Auckland, Auckland, New Zealand Observationof ovulatecones at thetime of pollinationin the southernconiferous family Podocarpaceaedemonstrates a distinctivemethod of pollencapture, involving an extended pollinationdrop. Ovules in all generaof the family are orthotropousand singlewithin the axil of each fertilebract. In Microstrobusand Phyllocladusovules are-erect (i.e., the micropyle directedaway from the cone axis) and are notassociated with an ovule-supportingstructure (epimatium).Pollen in thesetwo genera must land directly on thepollination drop in theway usualfor gymnosperms, as observed in Phyllocladus.In all othergenera, the ovule is inverted (i.e., the micropyleis directedtoward the cone axis) and supportedby a specializedovule- supportingstructure (epimatium). -
Inclusion of Taxaceae in a Separate Order, Taxales
OPINION Inclusion of Taxaceae in a separate order, Taxales D. D. Pant Taxus and its related genera, viz. Torreya, are common to the Pinales and their new times called taxinean spirals, but these Austrotaxus, Pseudotaxus and Amentotaxus order Taxales. The present article is occur in Cephalotaxus as well. were unquestionably included in the therefore intended to have a fresh look at Among characters of Taxus which have Pinales (= Coniferales) although they the similarities and differences between been mentioned as altogether different were usually included in a family of their Taxaceae and other conifers to enable us from those of all other Pinales, are its radi- own, the Taxaceae, inclusive of Cephalo- to decide whether we can continue to ally organized peltate microsporophylls taxus by Coulter & Chamberlain1 or ex- keep the Taxaceae as a family within the with sporangia attached on the adaxial, clusive of Cephalotaxus by Pilger2, Pinales or to include them in that family inner side. However, other genera of the who placed Cephalotaxus in a separate under a separate order, the Taxales. Taxaceae have dorsiventral microsporo- family, the Cephalotaxaceae. However, As Chamberlain6 had pointed out, ‘the phylls with microsporangia attached on in 1920, Sahni3 suggested that Taxus, grouping into families and sequence of the abaxial, underside like those of the Torreya and other closely-related genera families will depend upon each investi- Pinales. Thus, if we take the character of and Cephalotaxus were so different from gator. If he is an anatomist, anatomy will peltate microsporophylls into considera- other conifers and they should be inclu- determine the treatment. -
Holocene Vegetation History of a High- Elevation (1200 M) Site in the Lake Heron Basin, Inland Canterbury, New Zealand
Holocene vegetation history of a high-elevation site in the Lake Heron Basin, New Zealand 69 5 Holocene vegetation history of a high- elevation (1200 m) site in the Lake Heron Basin, inland Canterbury, New Zealand J. M. Pugh Department of Geological Sciences, University of Canterbury, Christchurch, New Zealand J. Shulmeister School of Geography, Planning and Environmental Management, University of Queensland, Australia [email protected] Introduction The Canterbury high country is a favourable location to examine climate-change histories because it lies in the lee of the Southern Alps. This causes the area to be a rain-shadow region and it is sensitive to changes in the strength and persistence of the regional westerly flow. Strong westerly flow is associated with droughts and high summer temperatures. In contrast, weakened westerly flow allows moisture from the east to penetrate these upland basins. As a consequence, this is an important area to study changes in the Southern Hemisphere westerly winds in this sector of the Southern Ocean. This record is unusual because it comes from near the natural tree line and as a consequence should be particularly sensitive to climate change and other environmental forcing. There are a number of significant palaeoecological questions that relate to this setting, including: (1) the persistence of montane podocarp woodland dominated by Phyllocladus and Halocarpus into the Holocene and the timing and cause of its subsequent replacement by beech forest; (2) the role played by fire in controlling vegetation structure and species composition; and (3) human impacts in the high country, especially with the transfer of high-country land into the conservation estate and consequential issues of ecological and landscape management (Armstrong et al. -
On the Flora of Australia
L'IBRARY'OF THE GRAY HERBARIUM HARVARD UNIVERSITY. BOUGHT. THE FLORA OF AUSTRALIA, ITS ORIGIN, AFFINITIES, AND DISTRIBUTION; BEING AN TO THE FLORA OF TASMANIA. BY JOSEPH DALTON HOOKER, M.D., F.R.S., L.S., & G.S.; LATE BOTANIST TO THE ANTARCTIC EXPEDITION. LONDON : LOVELL REEVE, HENRIETTA STREET, COVENT GARDEN. r^/f'ORElGN&ENGLISH' <^ . 1859. i^\BOOKSELLERS^.- PR 2G 1.912 Gray Herbarium Harvard University ON THE FLORA OF AUSTRALIA ITS ORIGIN, AFFINITIES, AND DISTRIBUTION. I I / ON THE FLORA OF AUSTRALIA, ITS ORIGIN, AFFINITIES, AND DISTRIBUTION; BEIKG AN TO THE FLORA OF TASMANIA. BY JOSEPH DALTON HOOKER, M.D., F.R.S., L.S., & G.S.; LATE BOTANIST TO THE ANTARCTIC EXPEDITION. Reprinted from the JJotany of the Antarctic Expedition, Part III., Flora of Tasmania, Vol. I. LONDON : LOVELL REEVE, HENRIETTA STREET, COVENT GARDEN. 1859. PRINTED BY JOHN EDWARD TAYLOR, LITTLE QUEEN STREET, LINCOLN'S INN FIELDS. CONTENTS OF THE INTRODUCTORY ESSAY. § i. Preliminary Remarks. PAGE Sources of Information, published and unpublished, materials, collections, etc i Object of arranging them to discuss the Origin, Peculiarities, and Distribution of the Vegetation of Australia, and to regard them in relation to the views of Darwin and others, on the Creation of Species .... iii^ § 2. On the General Phenomena of Variation in the Vegetable Kingdom. All plants more or less variable ; rate, extent, and nature of variability ; differences of amount and degree in different natural groups of plants v Parallelism of features of variability in different groups of individuals (varieties, species, genera, etc.), and in wild and cultivated plants vii Variation a centrifugal force ; the tendency in the progeny of varieties being to depart further from their original types, not to revert to them viii Effects of cross-impregnation and hybridization ultimately favourable to permanence of specific character x Darwin's Theory of Natural Selection ; — its effects on variable organisms under varying conditions is to give a temporary stability to races, species, genera, etc xi § 3. -
Podocarpaceae), from the Early Eocene of Laguna Del Hunco, Patagonia, Argentina
Australian Systematic Botany, 2019, 32, 290–309 ©CSIRO 2019 https://doi.org/10.1071/SB18043 Supplementary material A South American fossil relative of Phyllocladus: Huncocladus laubenfelsii gen. et sp. nov. (Podocarpaceae), from the early Eocene of Laguna del Hunco, Patagonia, Argentina Ana Andruchow-ColomboA,B,D, Peter WilfC and Ignacio H. EscapaA,B AMuseo Paleontológico Egidio Feruglio, Avenida Fontana 140, Trelew 9100, Chubut, Argentina. BConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Godoy Cruz 2290, C1425FQB, Ciudad Autónoma de Buenos Aires, Argentina. CDepartment of Geosciences, Pennsylvania State University, University Park, PA 16802, USA. DCorresponding author. Email: [email protected] Page 1 of 8 Australian Systematic Botany ©CSIRO 2019 https://doi.org/10.1071/SB18043 Fig. S1. A–C. Stomatal morphology of the extant species Phyllocladus aspleniifolius under light microscopy. A. General view of the cuticle showing the parallel oriented stomata arranged in discontinuous rows. B. Detail of the cuticle, showing rectangular epidermal cells arranged in rows; and the stomatal apparatuses parallel oriented, and arranged in discontinuous rows. C. Detail of a portion of the cuticle, showing stomatal apparatuses with four to six subsidiary cells, both polar and lateral, arranged in clear rings, and the well-developed Florin rings. Images provided by Dr G. J. Jordan. Scale bars: 500 μm (A), 200 μm (B) and 125 μm (C). Page 2 of 8 Australian Systematic Botany ©CSIRO 2019 https://doi.org/10.1071/SB18043 Character list Accession numbers for the DNA markers are the same than for Andruchow-Colombo et al. (2019). (00) Phyllotaxy of mature leaves: (0) helical; (1) whorled; (2) opposite to subopposite; (3) decussate; (4) opposite decussate. -
Forest to Fjaeldmark: Rainforest and Related Scrub
Edition 2 From Forest to Fjaeldmark The Vegetation Communities Rainforest and related scrub Eucryphia lucida Edition 2 From Forest to Fjaeldmark (revised – May 2018) 1 Rainforest and related scrub Community (Code) Page Athrotaxis cupressoides-Nothofagus gunnii short rainforest (RPF) 10 Athrotaxis cupressoides open woodland (RPW) 12 Athrotaxis cupressoides rainforest (RPP) 15 Athrotaxis selaginoides-Nothofagus gunnii short rainforest (RKF) 17 Athrotaxis selaginoides rainforest (RKP) 19 Athrotaxis selaginoides subalpine scrub (RKS) 21 Coastal rainforest (RCO) 23 Highland low rainforest and scrub (RSH) 25 Highland rainforest scrub with dead Athrotaxis selaginoides (RKX) 27 Lagarostrobos franklinii rainforest and scrub (RHP) 29 Nothofagus-Atherosperma rainforest (RMT) 31 Nothofagus-Leptospermum short rainforest (RML) 34 Nothofagus-Phyllocladus short rainforest (RMS) 36 Nothofagus gunnii rainforest scrub (RFS) 39 Nothofagus rainforest (undifferentiated) (RMU) 41 Rainforest fernland (RFE) 42 General description Diselma archeri and/or Pherosphaera hookeriana. These are mapped within the unit Highland This group comprises most Tasmanian vegetation coniferous shrubland (HCS), which is included within dominated by Tasmanian rainforest species (sensu the Highland treeless vegetation section. Jarman and Brown 1983) regardless of whether the dominant species are trees, shrubs or ferns. Rainforests and related scrub vegetation generally Tasmanian cool temperate rainforest has been occur in high rainfall areas of Tasmania that exceed defined floristically -
On the Ecology and Restoration of Podocarpus Cunninghamii in The
On the Ecology and Restoration of Podocarpus cunninghamii in the Eastern South Island High Country A thesis submitted in partial fulfilment of the requirements for the Degree of Doctor of Philosophy in the University of Canterbury by Alwyn Williams School of Forestry University of Canterbury 2010 Table of Contents List of Figures .............................................................................................................. vi List of Tables .............................................................................................................. vii List of Plates ............................................................................................................. viii Abstract ........................................................................................................................ ix Acknowledgements ...................................................................................................... x 1 Introduction ............................................................................................................... 1 1.1 The eastern South Island high country ................................................................. 1 1.3 Why restore Podocarpus cunninghamii? ............................................................. 8 1.3.1 Why we should restore Podocarpus cunninghamii forest ............................ 8 1.3.2 Why we need active restoration of Podocarpus cunninghamii forest ........ 11 1.4 Aims and objectives .......................................................................................... -
Review of Australia's Major Vegetation Classification and Descriptions
Review of Australia’s Major Vegetation Classification – CES, UNSW Hey k Review of Australia’s Major Vegetation classification and descriptions David A. Keith and Belinda J. Pellow Report to the Australian Department of the Environment 2015 1 Page Review of Australia’s Major Vegetation Classification – CES, UNSW Review of Australia’s Major Vegetation classification and descriptions Prepared by the Centre for Ecosystem Science (UNSW) in association with Australian Museum Consulting (AMC) for the Department of the Environment David A. Keith (Professor of Botany, UNSW) and Belinda J. Pellow (Senior Botanist, AMC) 30 June 2015 ISBN: 0-7334-3586-6 ISBN-13: 978-0-7334-3586-7 EAN: 9780733435867 Citation: Keith, D. A. & Pellow, B. J. (2015). Review of Australia’s Major Vegetation classification and descriptions. Centre for Ecosystem Science, UNSW, Sydney. Cover photos: D. Keith 2 Page Review of Australia’s Major Vegetation Classification – CES, UNSW Introduction The Australian Government, in collaboration with state and territory jurisdictions, maintains the National Vegetation Information System (NVIS), a repository for spatial data and associated thematic information on Australian native vegetation (NLWRA 2001; ESCVI 2003). NVIS includes a hierarchical database with some 18000 records of mapped vegetation types from all states and territories within Australia. The NVIS information hierarchy was augmented with an additional attribution of ‘Major Vegetation Groups’ (MVGs), enabling a high-level continental-scale synthesis to support the Australian Government’s reporting responsibilities under international agreements such as the Montreal and Kyoto Protocols (Montreal Process Implementation Group for Australia and National Forest Inventory Steering Committee 2013), and to inform the first national audit of native vegetation (NLWRA 2001). -
Podocarp Evolution: a Molecular Phylogenetic Perspective Edward Biffin, John G
1 Podocarp Evolution: A Molecular Phylogenetic Perspective Edward Biffin, John G. Conran, and Andrew J. Lowe ABSTRACT. Phylogenetic reconstructions of the relationships among extant taxa can be used to infer the nature of the processes that have generated contemporary patterns of biotic diversity. In this study, we present a molecular phylogenetic hypothesis for the conifer family Podocarpaceae based upon three DNA fragments that have been sampled for approximately 90 taxa. We use Bayesian relaxed- clock methods and four fossil con- straints to estimate divergence times among the lineages of Podocarpaceae. Our dating analyses suggest that although the family is old (Triassic–Jurassic), the extant species groups are of recent evolutionary origin (mid- to late Cenozoic), a pattern that could reflect a temporal increase in the rate lineage accumulation or, alternatively, a high and constant rate of extinction. Our data do not support the hypothesis that Podocarpaceae have diversified at a homogeneous rate, instead providing strong evidence for a three- to eightfold increase in diversification associated with the Podocarpoid– Dacrydioid clade, which radiated in the mid- to late Cretaceous to the earliest Cenozoic, around 60–94 mya. This group includes a predominance of taxa that develop broad leaves and/or leaf- like shoots and are distributed predominantly throughout the tropics. Tropical podocarps with broad leaves may have experienced reduced extinction and/or increased speciation coincident with the radiation of the angiosperms, the expansion of megathermal forests, and relatively stable tropical climates that were widespread through the Tertiary. Edward Biffin, John G. Conran, and Andrew J. INTRODUCTION Lowe, Australian Centre for Evolutionary Biol- ogy and Biodiversity, School of Earth and Envi- Patterns of species diversity reflect the balance of speciation and extinction ronmental Science, The University of Adelaide, Adelaide, South Australia 5005, Australia. -
Phylogenetic Relationships and Evolutionary History of the Southern Hemisphere Genus Leptinella Cass
Phylogenetic relationships and evolutionary history of the southern hemisphere genus Leptinella Cass. (Compositae, Anthemideae) Dissertation zur Erlangung des Doktorgrades der Naturwissenschaften (Dr. rer. nat.) der Naturwissenschaftlichen Fakultät III - Biologie und Vorklinische Medizin der Universität Regensburg vorgelegt von Sven Himmelreich aus Regensburg Regensburg, Juli 2009 Promotionsgesuch eingereicht am: 29.07.2009 Die Arbeit wurde angeleitet von: Prof. Dr. Christoph Oberprieler Prüfungsausschuss: Prüfungsausschussvorsitzender: Prof. Dr. Reinhard Wirth 1. Prüfer: Prof. Dr. Christoph Oberprieler 2. Prüfer: Prof. Dr. Günther Rudolf Heubl 3. Prüfer: Prof. Dr. Erhard Strohm Contents I Contents List of Figures II List of Tables III Acknowledgements IV Chapter 1 General Introduction 1 Chapter 2 Phylogeny of southern hemisphere Compositae-Anthemideae based 21 on nrDNA ITS and cpDNA ndhF sequence information Chapter 3 Phylogeny of Leptinella (Anthemideae, Compositae) inferred from 46 sequence information Chapter 4 Phylogenetic relationships in Leptinella (Anthemideae, 78 Compositae) inferred from AFLP fingerprinting Chapter 5 Evolution of dimorphic sex expression and polyploidy in Leptinella 107 Chapter 6 Conclusion 117 Summary 125 Zusammenfassung 128 References 131 Appendices 147 List of Figures II List of Figures Title Leptinella featherstonii on the Chatham Islands with Northern Royal Albatross (photo by P. de Lange, New Zealand). Fig. 1-1 Distribution of Leptinella based on Lloyd (1972c). 8 Fig. 1-2 Variation of plants in Leptinella. 9 Fig. 1-3 Capitula and florets of Leptinella. 9 Fig. 1-4 Leaves from different Leptinella taxa from cultivated plants. 10 Fig. 1-5 Postulate steps of the evolution of breeding systems in Leptinella 16 (modified from Lloyd 1975b). Fig. 2-1 Strict consensus tree of 493.976 equally most parsimonious trees 32 based on cpDNA ndhF sequence information. -
A New Classification and Linear Sequence of Extant Gymnosperms
Phytotaxa 19: 55–70 (2011) ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ Article PHYTOTAXA Copyright © 2011 Magnolia Press ISSN 1179-3163 (online edition) A new classification and linear sequence of extant gymnosperms MAARTEN J.M. CHRISTENHUSZ1, JAMES L. REVEAL2, ALJOS FARJON3, MARTIN F. GARDNER4, ROBERT R. MILL4 & MARK W. CHASE5 1Botanical Garden and Herbarium, Finnish Museum of Natural History, Unioninkatu 44, University of Helsinki, 00014 Helsinki, Finland. E-mail: [email protected] 2L. H. Bailey Hortorium, Department of Plant Biology, 412 Mann Building, Cornell University, Ithaca, NY 14853-4301, U.S.A. 3Herbarium, Library, Art & Archives, Royal Botanic Gardens, Kew, Richmond, Surrey, England, TW9 3AB, U.K. 4Royal Botanic Garden Edingurgh, 20A Inverleith Row, Edinburgh, EH3 5LR,Scotland, U.K. 5Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, Surrey, England, TW9 3DS, U.K. Abstract A new classification and linear sequence of the gymnosperms based on previous molecular and morphological phylogenetic and other studies is presented. Currently accepted genera are listed for each family and arranged according to their (probable) phylogenetic position. A full synonymy is provided, and types are listed for accepted genera. An index to genera assists in easy access to synonymy and family placement of genera. Introduction Gymnosperms are seed plants with an ovule that is not enclosed in a carpel, as is the case in angiosperms. The ovule instead forms on a leaf-like structure (perhaps homologous to a leaf), or on a scale or megasporophyll (homologous to a shoot) or on the apex of a (dwarf) shoot. Megasporophylls are frequently aggregated into compound structures that are often cone-shaped, hence the colloquial name for some of the group: conifers.