Conservation Advice Nematolepis Frondosa Leafy Nematolepis
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Patterns of Flammability Across the Vascular Plant Phylogeny, with Special Emphasis on the Genus Dracophyllum
Lincoln University Digital Thesis Copyright Statement The digital copy of this thesis is protected by the Copyright Act 1994 (New Zealand). This thesis may be consulted by you, provided you comply with the provisions of the Act and the following conditions of use: you will use the copy only for the purposes of research or private study you will recognise the author's right to be identified as the author of the thesis and due acknowledgement will be made to the author where appropriate you will obtain the author's permission before publishing any material from the thesis. Patterns of flammability across the vascular plant phylogeny, with special emphasis on the genus Dracophyllum A thesis submitted in partial fulfilment of the requirements for the Degree of Doctor of philosophy at Lincoln University by Xinglei Cui Lincoln University 2020 Abstract of a thesis submitted in partial fulfilment of the requirements for the Degree of Doctor of philosophy. Abstract Patterns of flammability across the vascular plant phylogeny, with special emphasis on the genus Dracophyllum by Xinglei Cui Fire has been part of the environment for the entire history of terrestrial plants and is a common disturbance agent in many ecosystems across the world. Fire has a significant role in influencing the structure, pattern and function of many ecosystems. Plant flammability, which is the ability of a plant to burn and sustain a flame, is an important driver of fire in terrestrial ecosystems and thus has a fundamental role in ecosystem dynamics and species evolution. However, the factors that have influenced the evolution of flammability remain unclear. -
National Recovery Plan for the Harsh Nematolepis Nematolepis Squamea Subspecies Coriacea
National Recovery Plan for the Harsh Nematolepis Nematolepis squamea subspecies coriacea Oberon Carter and Neville Walsh Prepared by Oberon Carter (Department of Sustainability and Environment, Victoria) and Neville Walsh (Royal Botanic Gardens, Melbourne). Published by the Victorian Government Department of Sustainability and Environment (DSE) Melbourne, November 2006. © State of Victoria Department of Sustainability and Environment 2006 This publication is copyright. No part may be reproduced by any process except in accordance with the provisions of the Copyright Act 1968. Authorised by the Victorian Government, 8 Nicholson Street, East Melbourne. ISBN 1 74152 305 2 This is a Recovery Plan prepared under the Commonwealth Environment Protection and Biodiversity Conservation Act 1999, with the assistance of funding provided by the Australian Government. This Recovery Plan has been developed with the involvement and cooperation of a range of stakeholders, but individual stakeholders have not necessarily committed to undertaking specific actions. The attainment of objectives and the provision of funds may be subject to budgetary and other constraints affecting the parties involved. Proposed actions may be subject to modification over the life of the plan due to changes in knowledge. Disclaimer This publication may be of assistance to you but the State of Victoria and its employees do not guarantee that the publication is without flaw of any kind or is wholly appropriate for your particular purposes and therefore disclaims all liability for any error, loss or other consequence that may arise from you relying on any information in this publication. An electronic version of this document is available on the DSE website www.dse.vic.gov.au For more information contact the DSE Customer Service Centre 136 186 Citation: Carter, O. -
Gardens and Stewardship
GARDENS AND STEWARDSHIP Thaddeus Zagorski (Bachelor of Theology; Diploma of Education; Certificate 111 in Amenity Horticulture; Graduate Diploma in Environmental Studies with Honours) Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy October 2007 School of Geography and Environmental Studies University of Tasmania STATEMENT OF AUTHENTICITY This thesis contains no material which has been accepted for any other degree or graduate diploma by the University of Tasmania or in any other tertiary institution and, to the best of my knowledge and belief, this thesis contains no copy or paraphrase of material previously published or written by other persons, except where due acknowledgement is made in the text of the thesis or in footnotes. Thaddeus Zagorski University of Tasmania Date: This thesis may be made available for loan or limited copying in accordance with the Australian Copyright Act of 1968. Thaddeus Zagorski University of Tasmania Date: ACKNOWLEDGEMENTS This thesis is not merely the achievement of a personal goal, but a culmination of a journey that started many, many years ago. As culmination it is also an impetus to continue to that journey. In achieving this personal goal many people, supervisors, friends, family and University colleagues have been instrumental in contributing to the final product. The initial motivation and inspiration for me to start this study was given by Professor Jamie Kirkpatrick, Dr. Elaine Stratford, and my friend Alison Howman. For that challenge I thank you. I am deeply indebted to my three supervisors Professor Jamie Kirkpatrick, Dr. Elaine Stratford and Dr. Aidan Davison. Each in their individual, concerted and special way guided me to this omega point. -
Cunninghamia Date of Publication: March 2016 a Journal of Plant Ecology for Eastern Australia
Cunninghamia Date of Publication: March 2016 A journal of plant ecology for eastern Australia ISSN 0727- 9620 (print) • ISSN 2200 - 405X (Online) Dieback of Nematolepis ovatifolia (Rutaceae), an endemic shrub in the alpine- subalpine heaths of the Snowy Mountains, is facilitated by climate change. K. Green NSW National Parks and Wildlife Service, Snowy Mountains Region, Jindabyne, 2627 AUSTRALIA [email protected] Abstract: The shrub Nematolepis ovatifolia (F. Muell.) Paul G. Wilson (family Rutaceae) is endemic to the alpine and subalpine areas of the Snowy Mountains, Australia, where it dominates large areas of heath. Mass dieback was observed in the spring/summer of 2012. Damage at first was confined to the tips of branches, a symptom that could be due to frost damage and/or pathogen-induced water stress. Subsequently, whole stems and shrubs died and new areas of chlorosis appeared on smaller shrubs. Surveys of 186 sites covering the geographical range of the shrub in the summers of 2013/14 and 2014/15 found that 59 populations were definitely dieback affected, 92 had early symptoms and 35 were healthy. Two possible causes were investigated: killing frost and pathogens, with insect attack being a further cause of defoliation. The root rot pathogen, Phytophthora cambivora was isolated from one washed root sample and from one of five soil/ root samples. In 2014/15, in five sites where symptomatic plants were monitored, most plants recovered to a condition where they were considered unaffected in March 2015. It is possible that symptomatic plants had in fact suffered frost damage. Hence populations with early symptoms were grouped with healthy populations for analysis of proximity to trails. -
National Recovery Plan for the Leafy Nematolepis Nematolepis Frondosa
National Recovery Plan for the Leafy Nematolepis Nematolepis frondosa Oberon Carter and Neville Walsh Prepared by Oberon Carter (Department of Sustainability and Environment, Victoria) and Neville Walsh (Royal Botanic Gardens, Melbourne). Published by the Victorian Government Department of Sustainability and Environment (DSE) Melbourne, November 2006. © State of Victoria Department of Sustainability and Environment 2006 This publication is copyright. No part may be reproduced by any process except in accordance with the provisions of the Copyright Act 1968. Authorised by the Victorian Government, 8 Nicholson Street, East Melbourne. ISBN 1 74152 299 4 This is a Recovery Plan prepared under the Commonwealth Environment Protection and Biodiversity Conservation Act 1999, with the assistance of funding provided by the Australian Government. This Recovery Plan has been developed with the involvement and cooperation of a range of stakeholders, but individual stakeholders have not necessarily committed to undertaking specific actions. The attainment of objectives and the provision of funds may be subject to budgetary and other constraints affecting the parties involved. Proposed actions may be subject to modification over the life of the plan due to changes in knowledge. Disclaimer This publication may be of assistance to you but the State of Victoria and its employees do not guarantee that the publication is without flaw of any kind or is wholly appropriate for your particular purposes and therefore disclaims all liability for any error, loss or other consequence that may arise from you relying on any information in this publication. An electronic version of this document is available on the DSE website www.dse.vic.gov.au For more information contact the DSE Customer Service Centre 136 186 Citation: Carter, O. -
A Phylogeny of the Rutaceae and a Biogeographic Study of Its Subfamily Aurantioideae
A phylogeny of the Rutaceae and a biogeographic study of its subfamily Aurantioideae Thomas Schwartz Supervisor Bernard Pfeil Degree project for Master of Science In Systematics and Biodiversity, Biology 60 hec Department of Plant and Environmental Science University of Gothenburg Abstract The Rutaceae classification is complex and has undergone several changes. In addition to morphological studies, phylogenetic inference using molecular data has also led to classification changes. Thus far only chloroplast data and ITS have been used, sometimes combined with morphology to infer the phylogeny. This study adds information from a low copy nuclear gene to test the existing phylogenetic hypothesis using a species tree framework. A biogeographic study was also performed on the Aurantioideae subfamily. A pilot study looked at the choice of genes, followed by testing and evaluation of several methods for extraction of Rutaceae DNA. Thereafter, a new method for efficient separation of alleles and paralogues was examined. The sequences obtained were analysed for recombination, positive selection and hybridisation. Trees for three loci (chloroplast, nuclear HYB and MDH) were made using MrBayes and BEAST, and a species tree was constructed with *BEAST. The *BEAST species tree is used as a template for a biogeographic study with the Lagrange geographic range likelihood analysis. A Bayesian biogeographic study is also performed using a Bayesian discrete biogeographical mode (an addition to BEAST). The results are then compared with previous studies, corroborating some and rejecting others. Sammanfattning Rutace-familjens struktur är komplex och föränderlig. Förutom morfologiska studier har även fylogenetiska studier använts för att få ordning i den. Hittills har man endast tittat på kloroplastgener och ribosom-DNA, i enstaka fall i kombination med morfologiska karaktärer. -
Action Statement
Action Statement Flora and Fauna Guarant ee Act 1988 No. 90 (Revised in 2008) Shiny Nematolepis Nematolepis wilsonii This revised Action Statement is based on the draft national Recovery Plan prepared for this species by DSE under contract to the Australian Government Department of the Environment, Water, Heritage and the Arts. Description Shiny Nematolepis ( Nematolepis wilsonii N.G. Walsh & Albr.) is a shrub or small tree which grows to 10 m high. This species was formerly known as Shiny Phebalium (Phebalium wilsonii ) (Elliot & Jones 1997). It resembles Satinwood ( Nematolepis squamea subsp. squamea ), which is largely restricted in Victoria to the Otway Ranges. Shiny Nematolepis can be distinguished from Satinwood by its glossy leaves, scaly petals and ovaries, and its branchlets which are covered in small protuberances (Costermans 1993). Distribution Shiny Nematolepis is a Victorian endemic, which was apparently first collected in 1892 and is Shiny Nematolepis (Photo: Downe) represented by a specimen at Melbourne Herbarium labelled ‘Goulburn R., Woods Point’. It was not formally described, however, until nearly 100 years later (Wilson 1970, Walsh and Albrecht 1988). The Woods Point record has not been substantiated this century and may be a result of vague locality recording by the original collector. Shiny Nematolepis is now known from a single population at the type locality, 720 m above sea level in the O'Shannassy Catchment, Yarra Ranges National Park. Habitat The population is scattered over an area of approximately five hectares. It is an understorey Distribution in Victoria component in Cool Temperate Mixed Forest which (Flora Information System DSE 2007) occurs between old-growth wet forest, dominated by Mountain Ash (Eucalyptus regnans ), and Cool Temperate Rainforest, dominated by Myrtle Beech (Nothofagus cunninghamii ). -
Divergence in Floral Morphology and Pollinator Interactions in Two Sympatric Australian Pea Plants
Divergence in floral morphology and pollinator interactions in two sympatric Australian pea plants Sarah Stock1 Abstract The diversification of flowering plants is often attributed to plant-pollinator interactions. Plants often evolve combinations of traits (collectively termed ‘pollinator syndromes’) which attract and utilise specific groups of insects. Oxylobium ellipticum (Vent, R.Br) and Hovea montana (Hook.f.) J.H.Ross are two Australian pea plants found in sympatry in Kosciuszko National Park. These plants differ in floral colour, but exhibit what appear to be identical mechanisms for accepting and depositing pollen from/to a pollinator. Through the analysis of floral morphology and pollinator activity it was found that these species have diverged in floral traits further than previously thought. Oxylobium ellipticum has larger keel petals resulting in a requirement for greater force to open flowers and the pressure point is found further from the base of the flower. These differences may be the result of reproductive competition leading to differential pollinator filtering systems or potentially divergent exploitation of the same pollinators. Key Words Fabaceae, Kosciuszko, pollination syndromes, reproductive competition Introduction The association between flower morphology and pollinators has been studied for over 200 years, and the diversification of flowering plants species has been linked to pollinator presence and behaviour (Johnson and Steiner 2000; Johnson 2010). In Australia, little study has been conducted on the pollination biology of legumes with papilionate flowers despite being a diverse family in southern Australia (but see Gross et al. 2000; Gross 2001). A central concept of pollination biology is pollination syndromes (Fenster et al. 2004). Pollination syndromes are defined as combinations of floral traits which are linked to attraction and exploitation of specific groups of pollinators (Fenster et al. -
Phytophthora Species Isolated from Alpine and Sub-Alpine Regions of Australia, Including the Description of Two New Species; Phytophthora Cacuminis Sp
Fungal Biology 123 (2019) 29e41 Contents lists available at ScienceDirect Fungal Biology journal homepage: www.elsevier.com/locate/funbio Phytophthora species isolated from alpine and sub-alpine regions of Australia, including the description of two new species; Phytophthora cacuminis sp. nov and Phytophthora oreophila sp. nov * Ihsanul Khaliq a, Giles E. St. J. Hardy a, Keith L. McDougall b, Treena I. Burgess a, a Centre for Phytophthora Science and Management, School of Veterinary and Life Sciences, Murdoch University, Perth, WA, 6150, Australia b Office of Environment and Heritage, PO Box 733, Queanbeyan, NSW 2620, Australia article info abstract Article history: Plant deaths had been observed in the sub-alpine and alpine areas of Australia. Although no detailed Received 28 August 2018 aetiology was established, patches of dying vegetation and progressive thinning of canopy suggested the Received in revised form involvement of root pathogens. Baiting of roots and associated rhizosphere soil from surveys conducted 10 October 2018 in mountainous regions New South Wales and Tasmania resulted in the isolation of eight Phytophthora Accepted 25 October 2018 species; Phytophthora cactorum, Phytophthora cryptogea, Phytophthora fallax, Phytophthora gonapodyides, Available online 1 November 2018 Phytophthora gregata, Phytophthora pseudocryptogea, and two new species, Phytophthora cacuminis sp. Corresponding Editor: Hermann Voglmayr nov and Phytophthora oreophila sp. nov, described here. P. cacuminis sp. nov is closely related to P. fallax, and was isolated from asymptomatic Eucalyptus coccifera and species from the family Proteaceae in Keywords: Mount Field NP in Tasmania. P. oreophila sp. nov, was isolated from a disturbed alpine herbfield in Cold adaptation Kosciuzsko National Park. The low cardinal temperature for growth of the new species suggest they are Cold environments well adapted to survive under these conditions, and should be regarded as potential threats to the Invasive potential diverse flora of sub-alpine/alpine ecosystems. -
Chilean Pitavia More Closely Related to Oceania and Old World Rutaceae
A peer-reviewed open-access journal PhytoKeys 19: 9–29Chilean (2012) Pitavia more closely related to Oceania and Old World Rutaceae... 9 doi: 10.3897/phytokeys.19.3912 RESEARCH ARTICLE www.phytokeys.com Launched to accelerate biodiversity research Chilean Pitavia more closely related to Oceania and Old World Rutaceae than to Neotropical groups: evidence from two cpDNA non-coding regions, with a new subfamilial classification of the family Milton Groppo1, Jacquelyn A. Kallunki2, José Rubens Pirani3, Alexandre Antonelli4 1 Departamento de Biologia, FFCLRP, Universidade de São Paulo, Av. Bandeirantes 3900, 14040-901 – Ribeirão Preto, SP, Brazil 2 The New York Botanical Garden, Bronx, NY, 10458-5126, USA 3 Instituto de Biociências, Universidade de São Paulo, Rua do Matão 277, 05508-090, São Paulo, SP, Brazil 4 Department of Biological and Environmental Sciences, University of Gothenburg, Carl Skottsbergs gata 22B, PO Box 461, 405 30 Gothenburg, Sweden Corresponding author: Milton Groppo ([email protected]) Academic editor: P. Acevedo-Rodríguez | Received 29 August 2012 | Accepted 5 December 2012 | Published 18 December 2012 Citation: Groppo M, Kallunki JA, Pirani JR, Antonelli A (2012) Chilean Pitavia more closely related to Oceania and Old World Rutaceae than to Neotropical groups: evidence from two cpDNA non-coding regions, with a new subfamilial classification of the family. PhytoKeys 19: 9–29. doi: 10.3897/phytokeys.19.3912 Abstract The position of the plant genus Pitavia within an infrafamilial phylogeny of Rutaceae (rue, or orange family) was investigated with the use of two non-coding regions from cpDNA, the trnL-trnF region and the rps16 intron. The only species of the genus, Pitavia punctata Molina, is restricted to the temperate forests of the Coastal Cordillera of Central-Southern Chile and threatened by loss of habitat. -
Plant, Invertebrate and Pathogen Interactions in Kosciuszko National Park
Plant, Invertebrate and Pathogen Interactions in Kosciuszko National Park KEITH L. MCDOUGALL1, GENEVIEVE T. WRIGHT1, TREENA I. BURGESS2, ROGER FARROW3, IHSAN KHALIQ2, MATTHEW H. LAURENCE4, THOMAS WALLENIUS5, AND EDWARD C. Y. LIEW4 1Offi ce of Environment and Heritage, PO Box 733, Queanbeyan NSW 2620; 2School of Veterinary and Life Sciences, Murdoch University, 90 South Street, Murdoch WA 6150; 3777 Urila Road, Urila NSW 2620 4The Royal Botanic Gardens and Domain Trust Sydney, Mrs Macquaries Road, Sydney NSW 2000; 5CSIRO Australian National Insect Collection, GPO Box 1700, Canberra, ACT 2601. Published on 15 November 2018 at https://openjournals.library.sydney.edu.au/index.php/LIN/index McDougall, K.L., Wright, G.T., Burgess, T.I., Farrow, R., Khaliq, I., Laurence, M.H., Wallenius, T. and Liew, E.C.Y. (2018). Plant, invertebrate and pathogen interactions in Kosciuszko National Park. Proceedings of the Linnean Society of New South Wales 140, 295-312. Kosciuszko National Park is the largest protected area in NSW and the only reserve in the State containing alpine vegetation. Diseases and pests of plants in the park are poorly known and, until recently, were thought to be benign and rare because of the cold climate. Surveys after the 2003 fi re that burnt about 70% of the park detected dieback in both unburnt and regenerating burnt shrubs and trees. Since then, 36 species of Phytophthora have been identifi ed in the park. Some perhaps do not persist but at least two (P. gregata and P. cambivora) are affecting the survival of two native shrub species. The fungus Armillaria luteobubalina also has been isolated from dying shrubs. -
Rutaceae) Based on Rbcl and Atpb Sequences
Major Clades of Australasian Rutoideae (Rutaceae) Based on rbcL and atpB Sequences Michael J. Bayly1*, Gareth D. Holmes1, Paul I. Forster2, David J. Cantrill3, Pauline Y. Ladiges1 1 School of Botany, The University of Melbourne, Parkville, Victoria, Australia, 2 Queensland Herbarium, Department of Science, Information Technology, Innovation and the Arts, Brisbane Botanic Gardens, Toowong, Queensland, Australia, 3 National Herbarium of Victoria, Royal Botanic Gardens Melbourne, South Yarra, Victoria, Australia Abstract Background: Rutaceae subfamily Rutoideae (46 genera, c. 660 species) is diverse in both rainforests and sclerophyll vegetation of Australasia. Australia and New Caledonia are centres of endemism with a number of genera and species distributed disjunctly between the two regions. Our aim was to generate a high-level molecular phylogeny for the Australasian Rutoideae and identify major clades as a framework for assessing morphological and biogeographic patterns and taxonomy. Methodology/Principal Findings: Phylogenetic analyses were based on chloroplast genes, rbcL and atpB, for 108 samples (78 new here), including 38 of 46 Australasian genera. Results were integrated with those from other molecular studies to produce a supertree for Rutaceae worldwide, including 115 of 154 genera. Australasian clades are poorly matched with existing tribal classifications, and genera Philotheca and Boronia are not monophyletic. Major sclerophyll lineages in Australia belong to two separate clades, each with an early divergence between rainforest and sclerophyll taxa. Dehiscent fruits with seeds ejected at maturity (often associated with myrmecochory) are inferred as ancestral; derived states include woody capsules with winged seeds, samaras, fleshy drupes, and retention and display of seeds in dehisced fruits (the last two states adaptations to bird dispersal, with multiple origins among rainforest genera).