On the Ecology and Restoration of Podocarpus Cunninghamii in The
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Morphology and Anatomy of Pollen Cones and Pollen in Podocarpus Gnidioides Carrière (Podocarpaceae, Coniferales)
1 2 Bull. CCP 4 (1): 36-48 (6.2015) V.M. Dörken & H. Nimsch Morphology and anatomy of pollen cones and pollen in Podocarpus gnidioides Carrière (Podocarpaceae, Coniferales) Abstract Podocarpus gnidioides is one of the rarest Podocarpus species in the world, and can rarely be found in collections; fertile material especially is not readily available. Until now no studies about its reproductive structures do exist. By chance a 10-years-old individual cultivated as a potted plant in the living collection of the second author produced 2014 pollen cones for the first time. Pollen cones of Podocarpus gnidioides have been investigated with microtome technique and SEM. Despite the isolated systematic position of Podocarpus gnidioides among the other New Caledonian Podocarps, it shows no unique features in morphology and anatomy of its hyposporangiate pollen cones and pollen. Both the pollen cones and the pollen are quite small and belong to the smallest ones among recent Podocarpus-species. The majority of pollen cones are unbranched but also a few branched ones are found, with one or two lateral units each of them developed from different buds, so that the base of each lateral cone-axis is also surrounded by bud scales. This is a great difference to other coniferous taxa with branched pollen cones e.g. Cephalotaxus (Taxaceae), where the whole “inflorescence” is developed from a single bud. It could be shown, that the pollen presentation in the erect pollen cones of Podocarpus gnidioides is secondary. However, further investigations with more specimens collected in the wild will be necessary. Key words: Podocarpaceae, Podocarpus, morphology, pollen, cone 1 Introduction Podocarpus gnidioides is an evergreen New Caledonian shrub, reaching up to 2 m in height (DE LAUBENFELS 1972; FARJON 2010). -
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. -
Interactive Effects of Climate Change and Species Composition on Alpine Biodiversity and Ecosystem Dynamics
Interactive effects of climate change and plant invasion on alpine biodiversity and ecosystem dynamics Justyna Giejsztowt M.Sc., 2013 University of Poitiers, France; Christian-Albrechts University, Germany B. Sc., 2010 University of Canterbury, New Zealand A thesis submitted to Victoria University of Wellington in partial fulfilment of the requirements for the degree of Doctor of Philosophy School of Biological Sciences Victoria University of Wellington Te Herenga Waka 2019 i ii This thesis was conducted under the supervision of Dr Julie R. Deslippe (primary supervisor) Victoria University of Wellington Wellington, New Zealand And Dr Aimée T. Classen (secondary supervisor) University of Vermont Burlington, United States of America iii iv “May your mountains rise into and above the clouds.” -Edward Abbey v vi Abstract Drivers of global change have direct impacts on the structure of communities and functioning of ecosystems, and interactions between drivers may buffer or exacerbate these direct effects. Interactions among drivers can lead to complex non-linear outcomes for ecosystems, communities and species, but are infrequently quantified. Through a combination of experimental, observational and modelling approaches, I address critical gaps in our understanding of the interactive effects of climate change and plant invasion, using Tongariro National Park (TNP; New Zealand) as a model. TNP is an alpine ecosystem of cultural significance which hosts a unique flora with high rates of endemism. TNP is invaded by the perennial shrub Calluna vulgaris (L.) Hull. My objectives were to: 1) determine whether species- specific phenological shifts have the potential to alter the reproductive capacity of native plants in landscapes affected by invasion; 2) determine whether the effect of invasion intensity on the Species Area Relationship (SAR) of native alpine plant species is influenced by environmental stress; 3) develop a novel modelling framework that would account for density-dependent competitive interactions between native species and C. -
The European Alpine Seed Conservation and Research Network
The International Newsletter of the Millennium Seed Bank Partnership August 2016 – January 2017 kew.org/msbp/samara ISSN 1475-8245 Issue: 30 View of Val Dosdé with Myosotis alpestris The European Alpine Seed Conservation and Research Network ELINOR BREMAN AND JONAS V. MUELLER (RBG Kew, UK), CHRISTIAN BERG AND PATRICK SCHWAGER (Karl-Franzens-Universitat Graz, Austria), BRIGITTA ERSCHBAMER, KONRAD PAGITZ AND VERA MARGREITER (Institute of Botany; University of Innsbruck, Austria), NOÉMIE FORT (CBNA, France), ANDREA MONDONI, THOMAS ABELI, FRANCESCO PORRO AND GRAZIANO ROSSI (Dipartimento di Scienze della Terra e dell’Ambiente; Universita degli studi di Pavia, Italy), CATHERINE LAMBELET-HAUETER, JACQUELINE DÉTRAZ- Photo: Dr Andrea Mondoni Andrea Dr Photo: MÉROZ AND FLORIAN MOMBRIAL (Conservatoire et Jardin Botaniques de la Ville de Genève, Switzerland). The European Alps are home to nearly 4,500 taxa of vascular plants, and have been recognised as one of 24 centres of plant diversity in Europe. While species richness decreases with increasing elevation, the proportion of endemic species increases – of the 501 endemic taxa in the European Alps, 431 occur in subalpine to nival belts. he varied geology of the pre and they are converting to shrub land and forest awareness of its increasing vulnerability. inner Alps, extreme temperature with reduced species diversity. Conversely, The Alpine Seed Conservation and Research T fluctuations at altitude, exposure to over-grazing in some areas (notably by Network currently brings together five plant high levels of UV radiation and short growing sheep) is leading to eutrophication and a science institutions across the Alps, housed season mean that the majority of alpine loss of species adapted to low nutrient at leading universities and botanic gardens: species are highly adapted to their harsh levels. -
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. -
The Evolution of Cavitation Resistance in Conifers Maximilian Larter
The evolution of cavitation resistance in conifers Maximilian Larter To cite this version: Maximilian Larter. The evolution of cavitation resistance in conifers. Bioclimatology. Univer- sit´ede Bordeaux, 2016. English. <NNT : 2016BORD0103>. <tel-01375936> HAL Id: tel-01375936 https://tel.archives-ouvertes.fr/tel-01375936 Submitted on 3 Oct 2016 HAL is a multi-disciplinary open access L'archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destin´eeau d´ep^otet `ala diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publi´esou non, lished or not. The documents may come from ´emanant des ´etablissements d'enseignement et de teaching and research institutions in France or recherche fran¸caisou ´etrangers,des laboratoires abroad, or from public or private research centers. publics ou priv´es. THESE Pour obtenir le grade de DOCTEUR DE L’UNIVERSITE DE BORDEAUX Spécialité : Ecologie évolutive, fonctionnelle et des communautés Ecole doctorale: Sciences et Environnements Evolution de la résistance à la cavitation chez les conifères The evolution of cavitation resistance in conifers Maximilian LARTER Directeur : Sylvain DELZON (DR INRA) Co-Directeur : Jean-Christophe DOMEC (Professeur, BSA) Soutenue le 22/07/2016 Devant le jury composé de : Rapporteurs : Mme Amy ZANNE, Prof., George Washington University Mr Jordi MARTINEZ VILALTA, Prof., Universitat Autonoma de Barcelona Examinateurs : Mme Lisa WINGATE, CR INRA, UMR ISPA, Bordeaux Mr Jérôme CHAVE, DR CNRS, UMR EDB, Toulouse i ii Abstract Title: The evolution of cavitation resistance in conifers Abstract Forests worldwide are at increased risk of widespread mortality due to intense drought under current and future climate change. -
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. -
Habitat and Diet of Kakapo (Strigops Habroptilis) in the Esperance Valley, Fiordland, New Zealand
37 Habitat and diet of kakapo (Strigops habroptilis) in the Esperance Valley, Fiordland, New Zealand IAN A.E. ATKINSON Abstract Vegetation in the Esperance Valley, Milford catchment, Fiordland, as 25 Wyndham Rd, Pinehaven, it was in February and March 1974, is described using quantitative data for part Upper Hutt, New Zealand. of the valley that included home ranges of two male kakapo (Strigops habroptilis). [email protected] One home range, of only 1.8 ha, was sited at 700 - 730 m altitude and extended over a gently-sloping river terrace covered in snow totara (Podocarpus nivalis) DON V. MERTON scrub with short silver beech (Nothofagus menziesii) forest at its margins. The other Honorary Research Associate, Research, home range was 4 ha in area, sited on a very steep (42°) valley wall mantled with Development and Improvement Division, unconsolidated avalanche debris at 800-860 m altitude, faced NW and was covered Department of Conservation, by Blechnum capense fern - shrubland and short silver beech forest communities. At PO Box 10-420, Wellington, New Zealand that time, this valley differed from most other parts of Fiordland: although possums (Trichosurus vulpecula), stoats (Mustela erminea) and rats (Rattus spp.) were present, ungulates were absent or very localised. Results gave no indication that food was limiting kakapo numbers in the Esperance Valley and we conclude that, because of the extreme vulnerability of females and their eggs, nestlings and fledglings to introduced mammalian predators, stoats were the most probable primary cause of kakapo decline in Fiordland. Atkinson, I.A.E.; Merton, D.V. 2006. Habitat and diet of kakapo (Strigops habroptilis) in the Esperance Valley, Fiordland, New Zealand. -
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. -
Examining the Competition Between Conifer and Angiosperm Trees Author(S): Timothy J
Elegance versus Speed: Examining the Competition between Conifer and Angiosperm Trees Author(s): Timothy J. Brodribb, Jarmila Pittermann, and David A. Coomes Reviewed work(s): Source: International Journal of Plant Sciences, Vol. 173, No. 6 (July/August 2012), pp. 673- 694 Published by: The University of Chicago Press Stable URL: http://www.jstor.org/stable/10.1086/666005 . Accessed: 09/07/2012 23:02 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]. The University of Chicago Press is collaborating with JSTOR to digitize, preserve and extend access to International Journal of Plant Sciences. http://www.jstor.org Int. J. Plant Sci. 173(6):673–694. 2012. Ó 2012 by The University of Chicago. All rights reserved. 1058-5893/2012/17306-0010$15.00 DOI: 10.1086/666005 ELEGANCE VERSUS SPEED: EXAMINING THE COMPETITION BETWEEN CONIFER AND ANGIOSPERM TREES Timothy J. Brodribb,1,* Jarmila Pittermann,y and David A. Coomesz *School of Plant Science, University of Tasmania, Hobart, Tasmania 7001, Australia; yDepartment of Ecology and Evolutionary Biology, University of California, Santa Cruz, California 95064, U.S.A.; and zForest Ecology and Conservation Group, Department of Plant Sciences, University of Cambridge, Downing Street, Cambridge CB2 3EA, United Kingdom Angiosperm radiation in the Cretaceous is thought to have profoundly diminished the success of the conifers, the other major woody plant group present at the time.