Southern Hemisphere Conifers - from Before the Flowering Plants
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Towards Land Cover Classification in Australia
Classifying Australian land cover C. Atyeo and R. Thackway December 2006 © Commonwealth of Australia 2006 This work is copyright. Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from the Commonwealth. Requests and inquiries concerning reproduction and rights should be addressed to the Commonwealth Copyright Administration, Attorney General’s Department, Robert Garran Offices, National Circuit, Barton ACT 2600 or posted at http://www.ag.gov.au/cca. The Australian Government acting through the Bureau of Rural Sciences has exercised due care and skill in the preparation and compilation of the information and data set out in this publication. Notwithstanding, the Bureau of Rural Sciences, its employees and advisers disclaim all liability, including liability for negligence, for any loss, damage, injury, expense or cost incurred by any person as a result of accessing, using or relying upon any of the information or data set out in this publication to the maximum extent permitted by law. Postal address: Bureau of Rural Sciences GPO Box 858 Canberra, ACT 2601 Copies available from: BRS Publication Sales GPO Box 858 Canberra ACT 2601 Ph: 1800 020 157 Fax: 02 6272 2330 Email: [email protected] Internet: http://www.brs.gov.au ii Acknowledgments The authors wish to thank the State and Territory representatives on the National Vegetation Information System Technical Advisory Group and the Executive Steering Committee for Australian Vegetation Information for endorsing the need to take a whole- of-landscape approach to translating and compiling native, non-native and non-vegetated cover types as part of the National Vegetation Information System framework. -
Species-Specific Basic Stem-Wood Densities for Twelve Indigenous Forest and Shrubland Species of Known Age, New Zealand
Marden et al. New Zealand Journal of Forestry Science (2021) 51:1 https://doi.org/10.33494/nzjfs512021x121x E-ISSN: 1179-5395 published on-line: 15/02/2021 Research Article Open Access New Zealand Journal of Forestry Science Species-specific basic stem-wood densities for twelve indigenous forest and shrubland species of known age, New Zealand Michael Marden1,*, Suzanne Lambie2 and Larry Burrows3 1 31 Haronga Road, Gisborne 4010, New Zealand 2 Manaaki Whenua – Landcare Research, Private Bag 3127, Hamilton 3240, New Zealand 3 Manaaki Whenua – Landcare Research, PO Box 69041, Lincoln 7640, New Zealand *Corresponding author: [email protected] (Received for publication 19 July 2019; accepted in revised form 26 January 2021) Abstract Background: Tree carbon estimates for New Zealand indigenous tree and shrub species are largely based on mean of sites throughout New Zealand. Yet stem-wood density values feed directly into New Zealand’s international and nationalbasic stem-wood greenhouse densities gas accounting. derived from We a limitedaugment number existing of publishedtrees, often basic of unspecified stem-wood age density and from data a limited with new number age- old, across 21 widely-distributed sites between latitudes 35° tospecific estimate values carbon for 12stocks. indigenous forest and shrubland species, including rarely obtained values for trees <6-years and 46° S, and explore relationships commonly used Methods: The volume of 478 whole stem-wood discs collected at breast height (BH) was determined by water displacement, oven dried, and weighed. Regression analyses were used to determine possible relationships between basic stem-wood density, and tree height, root collar diameter (RCD), and diameter at breast height (DBH). -
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). -
Forests and Scrublands of Northern Fiordland
80 Vol. 1 FORESTS AND SCRUBLANDS OF NORTHERN FIORDLAND J. WARDLE, J. HAYWARD, and J. HERBERT, Forest and Range Experiment Station, New Zealand Forest Service, Rangiora (Received for publication 18 January 1971) ABSTRACT The composition and structure of the forests and scrublands of northern Fiordland were recorded at 1,053 sample points. The vegetation at each sample point was classified into one of 16 associations using a combination of Sorensen's 'k' index of similarity, and a multi-linkage cluster analysis. The associations were related to habitat and the distribution of each was determined. The influence of the introduced ungulates, red deer and wapiti, on the forests and scrublands was determined. Stand structure was analysed to provide infor mation on the susceptibility of the vegetation to damage from browsing and on the history of ungulate utilisation of the vegetation. Browse indices were calculated to provide information on current ungulate utilisation of the vegetation. INTRODUCTION A reconnaissance of northern Fiordland was carried out during the summer of 1969-70 by staff of the Forest and Range Experiment Station. The purpose was to describe the composition, structure, and habitat of the forest and scrub associations, to determine both present and past influence of ungulates on them, and to establish a number of permanent reference points to permit measurement of future changes in the vegetation. The area studied lies between the western shores of Lake Te Anau and the Tasman Sea. The southern boundary is the South Fiord of Lake Te Anau, the Esk Burn and Windward River catchments, and Charles Sound; the northern boundary is the Worsley and Transit River catchments (Fig. -
Notification of Access Arrangement for MP 41279, Mt Te Kuha
Attachment C Draft Terrestrial Ecology Report 106 VEGETATION AND FAUNA OF THE PROPOSED TE KUHA MINE SITE Prepared for Te Kuha Limited Partnership October 2013 EXECUTIVE SUMMARY The Te Kuha mining permit is located predominantly within the Westport Water Conservation Reserve (1,825 ha), which is a local purpose reserve administered by the Buller District Council. The coal deposit is situated outside the water catchment within an area of approximately 490 ha of Brunner Coal Measures vegetation approximately 5 km southwest of Mt Rochfort. Access would be required across conservation land to reach the coal resource. The Te Kuha site was recommended as an area for protection by the Protected Natural Areas Programme surveys in the 1990s on the basis that in the event it was removed from the local purpose reserve for any reason, addition to the public conservation estate would increase the level of protection of coal measures habitats which, although found elsewhere (principally in the Mt Rochfort Conservation Area), were considered inadequately protected overall. The proposal to create an access road and an opencast mine at the site would affect twelve different vegetation types to varying degrees. The habitats present at the proposed mine site are overwhelmingly indigenous and have a very high degree of intactness reflecting their lack of human disturbance. Previous surveys have shown that some trees in the area are more than 500 years old. Habitats affected by the proposed access road are less intact and include exotic pasture as well as regenerating shrubland and forest. Te Kuha is not part of the Department of Conservation’s Buller Coal Plateaux priority site and is unlikely to receive management for that reason. -
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. -
Fire Retardant Plants for the Urban Fringe and Rural Areas
Flammability Groups Leptospermum scoparium TN Pittosporum undulatum AN X Cucurbita maxima E Pumpkin Morus sp. E Mulberry Manuka, Teatree Sweet Pittosporum Cymbopogon citratus E Lemon Grass Myoporum insulare AN Boobyalla In the following list E denotes an exotic plant, TN a plant Lomandra longifolia TN Saggs Platanus x acerifolia E Plane Tree Cyphomandra betacea E Tamarillo Nerium oleander E Oleander native to Tasmania, AN a plant native to mainland Australia Melaleuca alternifolia AN Paperbark Poa sp. AN Poa Grass Delonix regia E Poinciana Olearia argophylla TN Musk Monstera deliciosa E Monstera Populas sp. E Poplar and X a known environmental weed. Dicksonia antarctica TN Man Fern Photinia glabra var. rubens E Nadina domestica E Sacred Bamboo Quercus robur E English oak Diospryros sp. E Persimmon Chinese Fire Bush or Red-leafed Photinia High Flammability Nicotiana glauca AN Tobacco Bush Spiraea catoniensis E May Eriobotrya japonica E Loquat Pittosporum bicolor TN Cheesewood Pinus elliottii E Tasmannia lanceolata TN Escallonia macrantha E Escallonia These plants have been shown to be highly flammable and Slash or Elliott’s Pine Native Pepper Pteridium esculentum TN Euryops pectinatus E Bracken Fern should not be planted or allowed to remain inside your house’s Pinus patula E Ulex europaeus E X Gorse Yellow Daisy Bush Mexican or Weeping Pine Rhododendron sp. E Rhododendron Building Protection Zone. They should also be avoided in the Viburnum opulus E Guelder Rose Genista monspessulana E X Montpellier Broom Rosa sp. E X Roses, Briars Fuel Modified Zone. Move these plants away from your house Moderate Flammability Koelreuteria paniculata E Salix babylonica E Weeping Willow and replace them with less flammable plants. -
Ecology and Distribution of the Malesian Podocarps Neal J
4 Ecology and Distribution of the Malesian Podocarps Neal J. Enright and Tanguy Jaffré ABSTRACT. Podocarp species and genus richness is higher in the Malesian region than anywhere else on earth, with maximum genus richness in New Guinea and New Caledo- nia and maximum species richness in New Guinea and Borneo. Members of the Podo- carpaceae occur across the whole geographic and altitudinal range occupied by forests and shrublands in the region. There is a strong tendency for podocarp dominance of vegetation to be restricted either to high- altitude sites close to the limit of tree growth or to other sites that might restrict plant growth in terms of water relations and nutri- ent supply (e.g., skeletal soils on steep slopes and ridges, heath forests, ultramafic parent material). Although some species are widespread in lowland forests, they are generally present at very low density, raising questions concerning their regeneration ecology and competitive ability relative to co- occurring angiosperm tree species. A number of species in the region are narrowly distributed, being restricted to single islands or mountain tops, and are of conservation concern. Our current understanding of the distribution and ecology of Malesian podocarps is reviewed in this chapter, and areas for further research are identified. INTRODUCTION The Malesian region has the highest diversity of southern conifers (i.e., Podocarpaceae and Araucariaceae) in the world (Enright and Hill, 1995). It is a large and heterogeneous area, circumscribing tropical and subtropical lowland to montane forest (and some shrubland) assemblages, extending from Tonga in Neal J. Enright, School of Environmental Science, the east to India in the west and from the subtropical forests of eastern Australia Murdoch University, Murdoch, Western Austra- in the south to Taiwan and Nepal in the north (Figure 4.1). -
Habitat, Population Structure and the Conservation Status of Araucaria Bidwillii Hook
ResearchOnline@JCU This file is part of the following reference: Picone, Andrew Phillip (2014) Habitat, population structure and the conservation status of Araucaria bidwillii Hook. in the Australian Wet Tropics. PhD thesis, James Cook University. Access to this file is available from: http://researchonline.jcu.edu.au/44651/ The author has certified to JCU that they have made a reasonable effort to gain permission and acknowledge the owner of any third party copyright material included in this document. If you believe that this is not the case, please contact [email protected] and quote http://researchonline.jcu.edu.au/44651/ Habitat, population structure and the conservation status of Araucaria bidwillii Hook. in the Australian Wet Tropics. Thesis submitted by Andrew Phillip Picone (18856273) October 2015 For the degree of Masters in the College of Marine and Environmental Sciences James Cook University. ACKNOWLEDGEMENTS My supervisors Professor Paul Gadek, Dr Will Edwards and Dr Charles Clarke have demonstrated great patience in my part-time progress and provide support and guidance when sought. I’m particularly grateful for Prof. Gadek’s support for the original research proposal and shared interest in the Araucariaceae. The statistical approach was greatly improved under guidance from Dr Edwards and Dr Clarke provided invaluable advice on approaching the conservation assessment. Comments on overall style and structure were gratefully received from all supervisors. I’d also like to thank the College of Marine and Environmental Sciences at James Cook University. At the Wet Tropics Management Authority, Dr Steve Goosem and Mike Stott provided advice and data on vegetation mapping for Mount Lewis. -
Aridity Drove the Evolution of Extreme Embolism Resistance and The
Aridity drove the evolution of extreme embolism resistance and the radiation of conifer genus Callitris Maximilian Larter, Sebastian Pfautsch, Jean-Christophe Domec, Santiago Trueba, Nathalie Nagalingum, Sylvain Delzon To cite this version: Maximilian Larter, Sebastian Pfautsch, Jean-Christophe Domec, Santiago Trueba, Nathalie Na- galingum, et al.. Aridity drove the evolution of extreme embolism resistance and the radiation of conifer genus Callitris. New Phytologist, Wiley, 2017, 215 (1), pp.97-112. 10.1111/nph.14545. hal-01606790 HAL Id: hal-01606790 https://hal.archives-ouvertes.fr/hal-01606790 Submitted on 19 Nov 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution - ShareAlike| 4.0 International License Research Aridity drove the evolution of extreme embolism resistance and the radiation of conifer genus Callitris Maximilian Larter1, Sebastian Pfautsch2, Jean-Christophe Domec3,4, Santiago Trueba5,6, Nathalie Nagalingum7 and Sylvain Delzon1 1BIOGECO, INRA, Univ. Bordeaux, Pessac 33610, France; 2Hawkesbury Institute for the Environment, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia; 3Bordeaux Sciences AGRO, UMR 1391 ISPA INRA, 1 Cours du General de Gaulle, Gradignan Cedex 33175, France; 4Nicholas School of the Environment, Duke University, Durham, NC 27708, USA; 5Department of Ecology and Evolutionary Biology, University of California, Los Angeles, UCLA, 621 Charles E. -
Distribution and Ecology of the Conifers of New Caledonia
I 1 extrait de : EGOLQGY OP THE SOUTHERN CONIFERS Edited by : Neal J. ENRIGHT and Robert S. HILL MELBOW WVERSITY PRESS - 1935 5. - I Distribution and Ecology 8 of the Conifers of - New Caledonia T. JAFFRÉ ESPITE ITS small area (19 O00 km2) New Caledonia possesses a rich and distinctive flora, totalling 3000 species of phanerogams of which 75 to 80 per cent are endemic. Among these are 43 conifers (all endemic) belonging D (1 to four families: Taxaceae (one sp.), Podocarpaceae (18 spp.), Araucariaceae 8 spp.), Cupressaceae (six spp.). \ The sole species of the family Taxaceae belongs to the endemic genus Austrotaxus. The Podocarpaceae is divided among eight genera: Podocarpus (seven ii spp.), Dacrydium (four spp.), Retrophyllum (twospp.), Falcatifolium, Dacrycarpus, Acmopyb, Prumnopitys and Parasitaxus (one sp. each), the last being endemic to New Caledonia (Page 1988). The Araucariaceae comprises two genera, Araucaria (13 spp.) and Agathis (five spp.), and the Cupressaceae the genera Libocedrus (three spp.), Callitris (two spp.), and the monotypic and endemic Neocallitropsis (de Laubenfels 1972). No other region of the world with such a small area possesses such a rich and distinctive conifer flora. Growth forms The majority of New Caledonian conifers are tall trees but there are also small trees and shrubs. The Araucariaceae, all arborescent, includes nine species exploited for their timber (Agatbis corbassonii, A. lanceolata, A. moorei, A. ovata, Araucaria columnaris, A. bernieri, A. laubenfelsii, A. luxurians, A. subulata). The Agatbis species are among the most massive forest trees; some individuals I of the tallest species, Agatbis lanceolata, have trunks more than 2.5 m in diameter and attain a height of 30-40 m.