A Native Cottage Garden a Tropical Garden Using Local Native Plants
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PLANT COMMUNITY FIELD GUIDE Introduction to Rainforest
PLANT COMMUNITY FIELD GUIDE Introduction to Rainforest Communities Table of Contents (click to go to page) HCCREMS Mapping ....................................................................... 3 Field Data Sheet ............................................................................. 4 Which of the following descriptions best describes your site? ................................................................ 5 Which plant community is it? .......................................................... 9 Rainforest communities of the Lower Hunter .................................. 11 Common Rainforest Species of the Lower Hunter ........................................................................ 14 A picture guide to common rainforest species of the Lower Hunter ........................................................... 17 Weeding of Rainforest Remnants ................................................... 25 Rainforest Regeneration near Black Jacks Point ............................ 27 Protection of Rainforest Remnants in the Lower Hunter & the Re-establishment of Diverse, Indigenous Plant Communities ... 28 Guidelines for a rainforest remnant planting program ..................... 31 Threatened Species ....................................................................... 36 References ..................................................................................... 43 Acknowledgements......................................................................... 43 Image Credits ................................................................................ -
Anatomy and Affinities of Penthorum Melanie Lynn Haskins
University of Richmond UR Scholarship Repository Biology Faculty Publications Biology 2-1987 Anatomy and Affinities of Penthorum Melanie Lynn Haskins W. John Hayden University of Richmond, [email protected] Follow this and additional works at: http://scholarship.richmond.edu/biology-faculty-publications Part of the Botany Commons, Other Plant Sciences Commons, and the Plant Biology Commons Recommended Citation Haskins, Melanie Lynn, and W. John Hayden. "Anatomy and Affinities of Penthorum." American Journal of Botany 74, no. 2 (February 1987): 164-77. This Article is brought to you for free and open access by the Biology at UR Scholarship Repository. It has been accepted for inclusion in Biology Faculty Publications by an authorized administrator of UR Scholarship Repository. For more information, please contact [email protected]. Amer. J. Bot. 74(2): 164-177. 1987. ANATOMY AND AFFINITIES OF PENTHORUM' MELANIE L. HASKINS AND W. JOHN HAYDEN Department of Biology, University of Richmond, Richmond, Virginia 23173 ABSTRACT The genus Penthorum L. consists of two species of perennial herbs, P. sedoides of eastern North America and P. chinense ofeastern Asia. Pentho rum has long been considered intermediate between Crassulaceae and Saxifragaceae. An anatomical study of both species was undertaken to contribute to a better understanding of the relationships ofthese plants. Prominent anatomical features of Penthorum include: an aerenchymatous cortex and closely-spaced collateral vascular bundles of stems; one-trace unilacunar nodes; brochidodromous venation, rosoid teeth bearing hydathodes, and anomocytic stomata of leaves; angular vessel elements with many-barred scalariform perforation plates and alternate to scattered intervascular pits; thin-walled non septate fiber-tracheids; abundant homocellular erect uniseriate and biseriate rays; and absence of axial xylem parenchyma. -
Ancistrocladaceae
Soltis et al—American Journal of Botany 98(4):704-730. 2011. – Data Supplement S2 – page 1 Soltis, Douglas E., Stephen A. Smith, Nico Cellinese, Kenneth J. Wurdack, David C. Tank, Samuel F. Brockington, Nancy F. Refulio-Rodriguez, Jay B. Walker, Michael J. Moore, Barbara S. Carlsward, Charles D. Bell, Maribeth Latvis, Sunny Crawley, Chelsea Black, Diaga Diouf, Zhenxiang Xi, Catherine A. Rushworth, Matthew A. Gitzendanner, Kenneth J. Sytsma, Yin-Long Qiu, Khidir W. Hilu, Charles C. Davis, Michael J. Sanderson, Reed S. Beaman, Richard G. Olmstead, Walter S. Judd, Michael J. Donoghue, and Pamela S. Soltis. Angiosperm phylogeny: 17 genes, 640 taxa. American Journal of Botany 98(4): 704-730. Appendix S2. The maximum likelihood majority-rule consensus from the 17-gene analysis shown as a phylogram with mtDNA included for Polyosma. Names of the orders and families follow APG III (2009); other names follow Cantino et al. (2007). Numbers above branches are bootstrap percentages. 67 Acalypha Spathiostemon 100 Ricinus 97 100 Dalechampia Lasiocroton 100 100 Conceveiba Homalanthus 96 Hura Euphorbia 88 Pimelodendron 100 Trigonostemon Euphorbiaceae Codiaeum (incl. Peraceae) 100 Croton Hevea Manihot 10083 Moultonianthus Suregada 98 81 Tetrorchidium Omphalea 100 Endospermum Neoscortechinia 100 98 Pera Clutia Pogonophora 99 Cespedesia Sauvagesia 99 Luxemburgia Ochna Ochnaceae 100 100 53 Quiina Touroulia Medusagyne Caryocar Caryocaraceae 100 Chrysobalanus 100 Atuna Chrysobalananaceae 100 100 Licania Hirtella 100 Euphronia Euphroniaceae 100 Dichapetalum 100 -
University of Birmingham How Deep Is the Conflict Between Molecular And
University of Birmingham How deep is the conflict between molecular and fossil evidence on the age of angiosperms? Coiro, Mario; Doyle, James A.; Hilton, Jason DOI: 10.1111/nph.15708 License: None: All rights reserved Document Version Peer reviewed version Citation for published version (Harvard): Coiro, M, Doyle, JA & Hilton, J 2019, 'How deep is the conflict between molecular and fossil evidence on the age of angiosperms?', New Phytologist, vol. 223, no. 1, pp. 83-99. https://doi.org/10.1111/nph.15708 Link to publication on Research at Birmingham portal Publisher Rights Statement: Checked for eligibility 14/01/2019 This is the peer reviewed version of the following article: Coiro, M. , Doyle, J. A. and Hilton, J. (2019), How deep is the conflict between molecular and fossil evidence on the age of angiosperms?. New Phytol. , which has been published in final form at doi:10.1111/nph.15708. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. General rights Unless a licence is specified above, all rights (including copyright and moral rights) in this document are retained by the authors and/or the copyright holders. The express permission of the copyright holder must be obtained for any use of this material other than for purposes permitted by law. •Users may freely distribute the URL that is used to identify this publication. •Users may download and/or print one copy of the publication from the University of Birmingham research portal for the purpose of private study or non-commercial research. -
Glossary of Latin Roots
Botanical root meanings as compiled from website: www.prairienet.org/garden-gate/botrts.htm Glossary of Roots of Botanical Names Glossary Copyright © 1998-2003 Karen Fletcher ------------------------------------------------------------------------ Some word parts ("arizon-" and "terminal-") are (or should be ) obvious; others which seem obvious may be a case of "faux-amis" ("false friends"), as they say in French: Alpinia, a genus in the ginger family is NOT named for alpine regions, but rather for one Propser Alpinus, an Italian physician. I have not attempted to cover all forms of which a word-part might par- take, and I have purposefully varied the Latinized endings, even when I couldn't think of having encountered an example of, say, the neuter ending ("um") of a word-part. I've not given all POSSIBLE forms and endings for each part, rather my attempt has been to show (especially to the novice to all this "double-talk") the variety AMONG endings and hope that he will get a feel for not only the use of the word part but also its possible permutations, so that when he sees the word "procera" or "procerus" or "procerum," he will recognize it as meaning "tall," and when he encounters "bifrons" he will be able to put two parts together and get "two" and "leaf." And I've not even THOUGHT about including parts which honor proper names, such as "schottii, bernardii, farnesiana, berlandieri" etc. Most are somewhat obvious, and probably nothing to be done about those that aren't - except make this ditty many times its present length!. Most word parts here cited are usually prefixes and are denoted with the dash FOLLOWING the part; a few are mostly suffixes and, therefore, are cited with the dash preceding the part.) With suffixes, the desig- nation, "(...)" indicates that it is seldom the actual ending of the descriptive, and that it usually has one of the endings listed below. -
Interactions Among Leaf Miners, Host Plants and Parasitoids in Australian Subtropical Rainforest
Food Webs along Elevational Gradients: Interactions among Leaf Miners, Host Plants and Parasitoids in Australian Subtropical Rainforest Author Maunsell, Sarah Published 2014 Thesis Type Thesis (PhD Doctorate) School Griffith School of Environment DOI https://doi.org/10.25904/1912/3017 Copyright Statement The author owns the copyright in this thesis, unless stated otherwise. Downloaded from http://hdl.handle.net/10072/368145 Griffith Research Online https://research-repository.griffith.edu.au Food webs along elevational gradients: interactions among leaf miners, host plants and parasitoids in Australian subtropical rainforest Sarah Maunsell BSc (Hons) Griffith School of Environment Science, Environment, Engineering and Technology Griffith University Submitted in fulfilment of the requirements of the degree of Doctor of Philosophy February 2014 Synopsis Gradients in elevation are used to understand how species respond to changes in local climatic conditions and are therefore a powerful tool for predicting how mountain ecosystems may respond to climate change. While many studies have shown elevational patterns in species richness and species turnover, little is known about how multi- species interactions respond to elevation. An understanding of how species interactions are affected by current clines in climate is imperative if we are to make predictions about how ecosystem function and stability will be affected by climate change. This challenge has been addressed here by focussing on a set of intimately interacting species: leaf-mining insects, their host plants and their parasitoid predators. Herbivorous insects, including leaf miners, and their host plants and parasitoids interact in diverse and complex ways, but relatively little is known about how the nature and strengths of these interactions change along climatic gradients. -
Phylogeny and Phylogenetic Nomenclature of the Campanulidae Based on an Expanded Sample of Genes and Taxa
Systematic Botany (2010), 35(2): pp. 425–441 © Copyright 2010 by the American Society of Plant Taxonomists Phylogeny and Phylogenetic Nomenclature of the Campanulidae based on an Expanded Sample of Genes and Taxa David C. Tank 1,2,3 and Michael J. Donoghue 1 1 Peabody Museum of Natural History & Department of Ecology & Evolutionary Biology, Yale University, P. O. Box 208106, New Haven, Connecticut 06520 U. S. A. 2 Department of Forest Resources & Stillinger Herbarium, College of Natural Resources, University of Idaho, P. O. Box 441133, Moscow, Idaho 83844-1133 U. S. A. 3 Author for correspondence ( [email protected] ) Communicating Editor: Javier Francisco-Ortega Abstract— Previous attempts to resolve relationships among the primary lineages of Campanulidae (e.g. Apiales, Asterales, Dipsacales) have mostly been unconvincing, and the placement of a number of smaller groups (e.g. Bruniaceae, Columelliaceae, Escalloniaceae) remains uncertain. Here we build on a recent analysis of an incomplete data set that was assembled from the literature for a set of 50 campanulid taxa. To this data set we first added newly generated DNA sequence data for the same set of genes and taxa. Second, we sequenced three additional cpDNA coding regions (ca. 8,000 bp) for the same set of 50 campanulid taxa. Finally, we assembled the most comprehensive sample of cam- panulid diversity to date, including ca. 17,000 bp of cpDNA for 122 campanulid taxa and five outgroups. Simply filling in missing data in the 50-taxon data set (rendering it 94% complete) resulted in a topology that was similar to earlier studies, but with little additional resolution or confidence. -
Review of the Sporoderm Ultrastructure of Members of the Asterales S
ISSN 0031-0301, Paleontological Journal, 2006, Vol. 40, Suppl. 5, pp. S656–S663. © Pleiades Publishing, Inc., 2006. Review of the Sporoderm Ultrastructure of Members of the Asterales S. V. Polevova Biological Faculty, Moscow State University, Leninskie gory 1, Moscow, 119992 Russia e-mail: [email protected] Received March 23, 2006 Abstract—Palynomorphological characteristics of the order Asterales are discussed. Particular attention is paid to the pollen morphology of basal families of this group and to that of problematic taxa that are considered as sister groups to the group under study. Ultrastructurally similar sporoderms of several families, including (1) Asteraceae, Calyceraceae, and Goodeniaceae; (2) Campanulaceae, Phellinaceae, and Menyanthaceae; (3) Rousseaceae, Abrophyllaceae, and Columelliaceae, are described. Pollen grains of Alseuosmiaceae and Stylidiaceae show unique ultrastructural features of the exine. DOI: 10.1134/S0031030106110128 Key words: Asterales, pollen grains, ultrastructure, phylogenetic systematics. INTRODUCTION MATERIAL AND METHODS At different times, concepts of the group of Aster- Pollen grains of 18 members of 12 families were aceae and its relatives has been considered to include studied. The material was received from the herbarium different families. These variants concerned a distinct of Komarov Botanical Institution of the Russian Acad- circle of taxa. Thus, the system of Takhatajan (1997) emy of Sciences, St. Petersburg. included the subclass Asteridae with 14 families; the (1) Family Goodeniaceae: Brunonia australis system of Thorne (2000) included the suborder Astera- R. Brown and Dampiera eriocephala Vriese. nae with nine families. (2) Family Columelliaceae: Columellia sericea Recently, relationships of Asteraceae have been sig- F.A. Humbolt, A.J.A. Bonpland et C.S. -
Friends of the Koala Nursery
Friends of the Koala Nursery Rifle Range Road, East Lismore NSW 2480 (PO BOX 5034, East Lismore NSW 2480) * OPEN BY APPOINTMENT * Contact: Mark Wilson, Nursery Manager 0413 339 554 Email: [email protected] PLANT LIST – JUNE 2021 1. EUCALYPTS: (a) Koala food - price $1.00 (Commercial price $2.00) E. microcorys TALLOWOOD E. grandis FLOODED GUM E. robusta SWAMP MAHOGANY E. tereticornis FOREST RED GUM E. resinifera RED MAHOGANY E. siderophloia GREY IRONBARK E. saligna SYDNEY BLUE GUM E. propinqua GREY GUM E. acmenoides WHITE MAHOGANY E. dunni DUNN’S WHITE GUM E. amplifolia CABBAGE GUM E. racemosa SCRIBBLY GUM E. pilularis BLACKBUTT (b) Non-Koala food - prices as marked 2.00 Corymbia citriodora LEMON-SCENTED GUM 30m, lemon-scented foliage 2.00 Corymbia gummifera RED BLOODWOOD 30m large white flowers, good timber tree 1.50 Corymbia intermedia PINK BLOODWOOD 30m large white flowers, good timber tree 2.00 Corymbia maculata SPOTTED GUM 30m, good timber tree 2.00 Eucalyptus moluccana GREY BOX 25m mottled bark, good honey tree 2. SHRUBS: Order Price Variety Description 1.50 Acacia suaveolens SWEET-SCENTED WATTLE 1-2m, pale yellow sweetly scented flowers 3.00 Acmena ‘Allyn Magic’ DWARF LILLY-PILLY 50cm, burgundy new growth all year, 3.00 Acmena ‘Forest Flame’ 2-3m, lovely red new foliage, psyllid-free, great screen plant 3.00 Acmena smithii ‘Minipilly’ DWARF LILLY-PILLY 2m, red tips, great hedge or container plant 3.00 Astartea fascicularis ‘Pink’ 1m, pink flowers from Autumn to Summer 3.00 Austromyrtus ‘Copper Tops’ 1.2m, spreading shrub -
I Is the Sunda-Sahul Floristic Exchange Ongoing?
Is the Sunda-Sahul floristic exchange ongoing? A study of distributions, functional traits, climate and landscape genomics to investigate the invasion in Australian rainforests By Jia-Yee Samantha Yap Bachelor of Biotechnology Hons. A thesis submitted for the degree of Doctor of Philosophy at The University of Queensland in 2018 Queensland Alliance for Agriculture and Food Innovation i Abstract Australian rainforests are of mixed biogeographical histories, resulting from the collision between Sahul (Australia) and Sunda shelves that led to extensive immigration of rainforest lineages with Sunda ancestry to Australia. Although comprehensive fossil records and molecular phylogenies distinguish between the Sunda and Sahul floristic elements, species distributions, functional traits or landscape dynamics have not been used to distinguish between the two elements in the Australian rainforest flora. The overall aim of this study was to investigate both Sunda and Sahul components in the Australian rainforest flora by (1) exploring their continental-wide distributional patterns and observing how functional characteristics and environmental preferences determine these patterns, (2) investigating continental-wide genomic diversities and distances of multiple species and measuring local species accumulation rates across multiple sites to observe whether past biotic exchange left detectable and consistent patterns in the rainforest flora, (3) coupling genomic data and species distribution models of lineages of known Sunda and Sahul ancestry to examine landscape-level dynamics and habitat preferences to relate to the impact of historical processes. First, the continental distributions of rainforest woody representatives that could be ascribed to Sahul (795 species) and Sunda origins (604 species) and their dispersal and persistence characteristics and key functional characteristics (leaf size, fruit size, wood density and maximum height at maturity) of were compared. -
Phylogenetic Studies in the Euasterids II
Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 676 _____________________________ _____________________________ Phylogenetic Studies in the Euasterids II with Particular Reference to Asterales and Escalloniaceae BY JOHANNES LUNDBERG ACTA UNIVERSITATIS UPSALIENSIS UPPSALA 2001 Dissertation for the Degree of Doctor of Philosophy in Systematic Botany presented at Uppsala University in 2002 Abstract Lundberg, J. 2001. Phylogenetic studies in the Euasterids II with particular reference to Asterales and Escalloniaceae. Acta Univ. Ups. Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology 676. 38 pp. Uppsala. ISBN 91-554-5191-8. The present study is concerned with the evolutionary relationships among the Euasterids II, a group of angiosperms that includes the orders Apiales, Aquifoliales, Asterales, and Dipsacales together with several small, poorly known families yet unplaced as to order. Parsimony analysis of nucleotide sequence data from the chloroplast genes atpB, ndhF and rbcL together with morphological data are used to construct a phylogeny of the order Asterales, which in the present sense includes 11 families and more than 26 000 species. It is argued that Rousseaceae should be expanded to include also Carpodetaceae (and thus contain four genera), and that Donatia should be re-merged with Stylidiaceae. The present study also strongly supports that the sister taxon to the largest plant family, Asteraceae (Compositae), is the small South American Calyceraceae. A new addition to Asterales is Platyspermation (formerly in Escalloniaceae). Using the recently developed Bayesian approach to phylogenetic reconstruction, in combination with a dataset consisting of the atpB, ndhF and rbcL nucleotide sequences, a resolved and fairly well supported phylogeny of the Euasterids II was reconstructed. -
Dioecy, Self-Compatibility and Vegetative Reproduction in Australian Subtropical Rainforest Trees and Shrubs
89 Dioecy, self-compatibility and vegetative reproduction in Australian subtropical rainforest trees and shrubs Paul Adam1 and Geoff Williams1,2 Adam, Paul 1 and Williams, Geoff 1,2 ( 1School of Biological Sciences, University of New South Wales, Kensington, NSW, Australia 2052, 2c/o Department of Entomology, Australian Museum, 6 College Street, Sydney, NSW, Australia 2000) 2001. Dioecy, self- compatibility and vegetative reproduction in Australian subtropical rainforest trees and shrubs. Cunninghamia 7(1): 89–100. Australian subtropical rainforests and plant populations have become increasingly fragmented since European settlement. Managing relict populations and remnants within the landscape matrix is dependent upon our understanding of plant reproductive biology. The incidence of autogamous self-compatibility and dioecy was investigated in subtropical rainforests, near Taree, in the Manning Valley (northern New South Wales). The proportion of dioecious species in rainforests of the region is high (~17%), but varies among sites. The potential for hermaphroditic species to self-pollinate was examined by bagging inflorescences in the field. Of the > 30 species (in 14 families) studied, nine species exhibited high levels of self- compatibility. These were predominantly pioneer and edge species, but other pioneer species were self-incompatible. Different behaviour occurred within families. Twenty species (in 13 families) regenerated from basal coppice or root suckers following bushfire. The significance of knowledge of reproductive biology for management is discussed. Introduction Many tropical and subtropical trees and shrubs are characterised by wide geographical distributions, but at individual sites species often have low population densities. During the Tertiary subtropical rainforest was very extensive in Australia (Adam 1992). In recent geological time its distribution has become limited and fragmented, as much of Australia became arid, with fluctuations in extent driven by climatic change during glacial-interglacial cycles.