Phytophthora Science and Management in Western Australia
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WRA Species Report
Family: Xanthorrhoeaceae Taxon: Xanthorrhoea preissii Synonym: Xanthorrhoea reflexa D.A.Herb. Common Name: Balga Xanthorrhoea pecoris F.Muell. Grass Tree Questionaire : current 20090513 Assessor: Chuck Chimera Designation: L Status: Assessor Approved Data Entry Person: Chuck Chimera WRA Score -5 101 Is the species highly domesticated? y=-3, n=0 n 102 Has the species become naturalized where grown? y=1, n=-1 103 Does the species have weedy races? y=1, n=-1 201 Species suited to tropical or subtropical climate(s) - If island is primarily wet habitat, then (0-low; 1-intermediate; 2- Intermediate substitute "wet tropical" for "tropical or subtropical" high) (See Appendix 2) 202 Quality of climate match data (0-low; 1-intermediate; 2- High high) (See Appendix 2) 203 Broad climate suitability (environmental versatility) y=1, n=0 n 204 Native or naturalized in regions with tropical or subtropical climates y=1, n=0 n 205 Does the species have a history of repeated introductions outside its natural range? y=-2, ?=-1, n=0 y 301 Naturalized beyond native range y = 1*multiplier (see n Appendix 2), n= question 205 302 Garden/amenity/disturbance weed n=0, y = 1*multiplier (see Appendix 2) 303 Agricultural/forestry/horticultural weed n=0, y = 2*multiplier (see n Appendix 2) 304 Environmental weed n=0, y = 2*multiplier (see n Appendix 2) 305 Congeneric weed n=0, y = 1*multiplier (see n Appendix 2) 401 Produces spines, thorns or burrs y=1, n=0 n 402 Allelopathic y=1, n=0 n 403 Parasitic y=1, n=0 n 404 Unpalatable to grazing animals y=1, n=-1 n 405 Toxic -
Clock Model Makes a Large Difference to Age Estimates of Long-Stemmed
Crisp et al. BMC Evolutionary Biology 2014, 14:263 http://www.biomedcentral.com/1471-2148/14/263 RESEARCH ARTICLE Open Access Clock model makes a large difference to age estimates of long-stemmed clades with no internal calibration: a test using Australian grasstrees Michael D Crisp1*, Nate B Hardy2 and Lyn G Cook3 Abstract Background: Estimating divergence times in phylogenies using a molecular clock depends on accurate modeling of nucleotide substitution rates in DNA sequences. Rate heterogeneity among lineages is likely to affect estimates, especially in lineages with long stems and short crowns (?broom?clades) and no internal calibration. We evaluate the performance of the random local clocks model (RLC) and the more routinely employed uncorrelated lognormal relaxed clock model (UCLN) in situations in which a significant rate shift occurs on the stem branch of a broom clade. We compare the results of simulations to empirical results from analyses of a real rate-heterogeneous taxon ? Australian grass trees (Xanthorrhoea) ?whose substitution rate is slower than in its sister groups, as determined by relative rate tests. Results: In the simulated datasets, the RLC model performed much better than UCLN: RLC correctly estimated the age of the crown node of slow-rate broom clades, whereas UCLN estimates were consistently too young. Similarly, in the Xanthorrhoea dataset, UCLN returned significantly younger crown ages than RLC (mean estimates respectively 3?6 Ma versus 25?35 Ma). In both real and simulated datasets, Bayes Factor tests strongly favored the RLC model over the UCLN model. Conclusions: The choice of an unsuitable molecular clock model can strongly bias divergence time estimates. -
Western Australian Natives Susceptible to Phytophthora Cinnamomi
Western Australian natives susceptible to Phytophthora cinnamomi. Compiled by E. Groves, G. Hardy & J. McComb, Murdoch University Information used to determine resistance to P. cinnamomi : 1a- field observations, 1b- field observation and recovery of P.cinnamomi; 2a- glasshouse inoculation of P. cinnamomi and recovery, 2b- field inoculation with P. cinnamomi and recovery. Not Provided- no information was provided from the reference. PLANT SPECIES COMMON NAME ASSESSMENT RARE NURSERY REFERENCES SPECIES AVALABILITY Acacia campylophylla Benth. 1b 15 Acacia myrtifolia (Sm.) Willd. 1b A 9 Acacia stenoptera Benth. Narrow Winged 1b 16 Wattle Actinostrobus pyramidalis Miq. Swamp Cypress 2a 17 Adenanthos barbiger Lindl. 1a A 1, 13, 16 Adenanthos cumminghamii Meisn. Albany Woolly Bush NP A 4, 8 Adenanthos cuneatus Labill. Coastal Jugflower 1a A 1, 6 Adenanthos cygnorum Diels. Common Woolly Bush 2 1, 7 Adenanthos detmoldii F. Muell. Scott River Jugflower 1a 1 Adenanthos dobagii E.C. Nelson Fitzgerald Jugflower NP R 4,8 Adenanthos ellipticus A.S. George Oval Leafed NP 8 Adenanthos Adenanthos filifolius Benth. 1a 19 Adenanthos ileticos E.C. George Club Leafed NP 8 Adenanthos Adenanthos meisneri Lehm. 1a A 1 Adenanthos obovatus Labill. Basket Flower 1b A 1, 7 14,16 Adenanthos oreophilus E.C. Nelson 1a 19 Adenanthos pungens ssp. effusus Spiky Adenanthos NP R 4 Adenanthos pungens ssp. pungens NP R 4 Adenanthos sericeus Labill. Woolly Bush 1a A 1 Agonis linearifolia (DC.) Sweet Swamp Peppermint 1b 6 Taxandria linearifolia (DC.) J.R Wheeler & N.G Merchant Agrostocrinum scabrum (R.Br) Baill. Bluegrass 1 12 Allocasuarina fraseriana (Miq.) L.A.S. Sheoak 1b A 1, 6, 14 Johnson Allocasuarina humilis (Otto & F. -
Species of Phytophthora Associated with a Native Ecosystem in Gauteng
Species of Phytophthora associated with a native ecosystem in Gauteng by Jan Hendrik Nagel BSc Genetics (Hons) Submitted in partial fulfilment of the requirements for the degree Magister Scientiae In the Faculty of Natural & Agricultural Sciences, Department of Genetics, University of Pretoria, Pretoria September 2012 Supervisor: Dr. Marieka Gryzenhout Co-supervisors: Prof. Bernard Slippers Prof. Michael J. Wingfield i Declaration I, Jan Hendrik Nagel, declare that the thesis/dissertation, which I hereby submit for the degree Magister Scientiae at the University of Pretoria, is my own work and has not previously been submitted by me for a degree at this or any other tertiary institution. SIGNATURE: ___________________________ DATE: ________________________________ ii TABLE OF CONTENTS ACKNOWLEDGEMENTS 1 PREFACE 2 CHAPTER 1 4 DIVERSITY , SPECIES RECOGNITION AND ENVIRONMENTAL DETECTION OF Phytophthora spp. 1. INTRODUCTION 6 2. THE OOMYCETES 7 2.1. OOMYCETES VERSUS FUNGI 7 2.2. TAXONOMY OF OOMYCETES 7 2.3. DIVERSITY AND IMPACT OF OOMYCETES 9 2.4. IMPACT OF Phytophthora 11 3. SPECIES RECOGNITION IN Phytophthora 13 3.1. MORPHOLOGICAL SPECIES CONCEPT 14 3.2. BIOLOGICAL SPECIES CONCEPT 14 3.3. PHYLOGENETIC SPECIES CONCEPT 15 4. STUDYING Phytophthora IN NATIVE ECOSYSTEMS 17 4.1. ISOLATION AND CULTURE OF Phytophthora 17 4.2. MOLECULAR DETECTION AND IDENTIFICATION TECHNIQUES FOR Phytophthora 19 4.3. RESTRICTION FRAGMENT LENGTH POLYMORPHISM (RFLP) 19 4.4. SINGLE -STRAND CONFORMATION POLYMORPHISM (SSCP) 20 4.5. PCR DETECTION WITH SPECIES -SPECIFIC PRIMERS 21 4.6. QUANTATIVE PCR 22 4.7. DNA HYBRIDIZATION BASED TECHNIQUES 23 4.8. SEROLOGICAL TECHNIQUES 24 4.9. PCR AMPLIFICATION WITH GENUS SPECIFIC PRIMERS 25 5. -
1 Description and Assessment of the Nature Conservation
DESCRIPTION AND ASSESSMENT OF THE NATURE CONSERVATION VALUES OF BENJE-BENJENUP LAKE AND ADJACENT BUSHLAND 1.0 INTRODUCTON Lake Benje-Benjenup and its adjacent bushland are located 17 km north north east of Esperance on the south east coast of WA. The lake is within unvested reserve no. 14563 of 149 ha gazetted in 1913 for ‘water’. The lake has maximum dimensions of 1.2 x 1.0 km and an area of approximately 90 ha. The adjacent bushland is to the east of the lake on Esperance location 650, which is privately owned by N & P Blumann and part of the farming property ‘Olimarena’. Approximately 85 ha of 130 ha of remnant bush is the subject of this assessment. ‘Benje-Benjenup’ is of aboriginal derivation, the meaning is unrecorded by Department of Land Information; the name was first used for the lake on a plan drafted by surveyor R Brazier in 1894. The regional setting of the lake is in Coramup Creek catchment, a sub-catchment of the Lake Warden system of southward flowing drainages and high value coastal wetlands including Lakes Warden, Woody and part of Lake Mullett which are RAMSAR wetlands. However, the lake appears to function as an internally draining system independent of the larger catchment; it is fed by brackish seepages along the shoreline and a saline creek of approximately 6 km length entering from the north west. Benje-Benjenup Lake is described as a ‘permanent saline lake’ in fair condition, requiring significant management intervention in the biodiversity audit of WA’s Biogeographical Regions (May & McKenzie 2002). -
B14. Pathogen Management
B14. Pathogen Management Phytophthora Dieback What is Phytophthora Dieback? There are over 120 described species of Phytophthora in the world, but the species that causes the most severe and widespread damage to native plants in Western Australia is Phytophthora cinnamomi. Phytophthora Dieback refers to the plant disease caused by P. cinnamomi, an introduced soil borne plant pathogen that poses a serious threat to vegetation. This pathogen is recognised by the Commonwealth's Environmental Protection and Biodiversity Conservation Act 1999 as a ‘key threatening process' to Australia's biodiversity. Phytophthora Dieback is arguably the greatest biological threat to biodiversity throughout the South-West region in Western Australia. Infestations have been recorded from Geraldton in the north, to east of Esperance in the south with the disease causing death to 40-50 per cent of native plant species in this region. Where does Phytophthora Dieback exist? Phytophthora cinnamomi, considered to have originated from South-East Asia, is now found around the world causing disease in native and introduced plant species alike. In the south-west of WA it is found in areas receiving more than 400 mm annual rainfall between Jurien and east of Esperance. Phytophthora dieback is found all around the Perth metropolitan area causing disease in our native banksia woodlands and jarrah forests as well as affecting plants in private and public gardens, and street-scapes. The establishment and spread of the pathogen is most common in wetter, neutral to acidic soils common to the Bassendean sands and Darling Scarp. While less common in the well- drained alkaline soils of the western coastal dune systems, amended soils such as public or private gardens and pockets of acidic duplex soils can still be susceptible to the disease. -
Flora of Australia, Volume 46, Iridaceae to Dioscoreaceae
FLORA OF AUSTRALIA Volume 46 Iridaceae to Dioscoreaceae This volume was published before the Commonwealth Government moved to Creative Commons Licensing. © Commonwealth of Australia 1986. This work is copyright. You may download, display, print and reproduce this material in unaltered form only (retaining this notice) for your personal, non-commercial use or use within your organisation. Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced or distributed by any process or stored in any retrieval system or data base without prior written permission from the copyright holder. Requests and inquiries concerning reproduction and rights should be addressed to: [email protected] FLORA OF AUSTRALIA The nine families in this volume of the Flora of Australia are Iridaceae, Aloeaceae, Agavaceae, Xanthorrhoeaceae, Hanguan- aceae, Taccaceae, Stemonaceae, Smilacaceae and Dioscoreaceae. The Xanthorrhoeaceae has the largest representation with 10 genera and 99 species. Most are endemic with a few species of Lomandra and Romnalda extending to neighbouring islands. The family includes the spectacular blackboys and grass-trees. The Iridaceae is largely represented by naturalised species with 52 of the 78 species being introduced. Many of the introductions are ornamentals and several have become serious weeds. Patersonia is the largest genus with all 17 species endemic. Some of these are cultivated as ornamentals. The Dioscoreaccae is a family of economic significance, particularly in the old world tropics where some species are cultivated or collected for their tubers and bulbils. In Australia there are 5 species, one of which is a recent introduction. The endemic and native species, commonly known as yams, are traditionally eaten by the Aborigines. -
Phenology and Growth of the Grasstree Xanthorrhoea Preissii in Relation to Fire and Season
Department of Environmental Biology Phenology and Growth of the Grasstree Xanthorrhoea preissii in Relation to Fire and Season Dylan Korczynskyj This thesis is presented as part of the requirements for the award of Doctor of Philosophy of Curtin University of Technology June 2002 i DECLARATION This thesis contains no material which has been accepted for the award of any other degree or diploma in any university. To the best of my knowledge and belief this thesis contains no material previously published by any other person except where due acknowledgment has been made. Dylan Korczynskyj 2 June 2002 ii Abstract Australian grasstrees are a long-lived group of arborescent, monocotyledonous plants that persist in fire-prone landscapes. Renowned for their capacity to survive fire, and flower soon after, these species have long attracted the attention of biologists. A southwestern Australian species, Xanthorrhoea preissii, has been the subject of several recent studies, including use and verification of the “leafbase banding technique” that prompted my study. This technique, which is used to determine the age and fire history of grasstrees, correlates alternating brown- and cream-coloured, transverse bands along the stem of grasstrees with seasonal growth, and intermittent black bands with the burning of the plant. Combined, this information provides a chronology for the fire events. Fundamental to this interpretation is the assumption that grasstrees grow continually, and this growth varies annually in accordance with changes between the two contrasting seasons of its mediterranean climate. I studied X. preissii in two habitats (jarrah forest and banksia woodland) adjacent to the Perth metropolitan area, in southwestern Australia, focussing on leaf growth and phenology in relation to four factors important to the species lifecycle; climate, fire, reproduction and herbivory. -
Western Australian Natives Susceptible to Phytophthora Cinnamomi
Appendix 2 Western Australian Natives Susceptible to Phytophthora cinnamomi. Compiled by E. Groves, P. Hollick, G. Hardy & J. McComb, Murdoch University Information used to determine susceptibility to P. cinnamomi: 1a- field observations, 1b- field observation and recovery of P.cinnamomi. 2a- glasshouse inoculation of P. cinnamomi and recovery, 2b- field inoculation with P. cinnamomi and recovery. NP- no information was given in the reference . RARE NURSERY PLANT SPECIES COMMON NAME ASSESSMENT SPECIES AVAILABILITY REFERENCES (R) (A) Acacia campylophylla Benth. 1b 27 Acacia myrtifolia (Sm) wild. 1b A 14 Acacia stenoptera Maslin. Narrow Winged Wattle 1b 28 Actinostrobus pyramidalis Miq. Swamp Cypress 2a 31 Adenanthos barbiger Lindl. 1a A 1, 18, 28 Adenanthos cumminghamii Meisn. Albany Woolly Bush NP A 8, 12 Adenanthos cuneatus Labill. Coastal Jugflower 1a A 1, 10 Adenanthos cygnorum Diels. Common Woolly Bush 1a 1, 11 Adenanthos detmoldii F. Muell. Scott River Jugflower 1a 1 Adenanthos dobagii E.C. Nelson Fitzgerald Jugflower NP R 8, 12 Adenanthos ellipticus A.S. George Oval Leafed Adenanthos NP 12 Adenanthos filifolius Benth. 1a 33 Adenanthos ileticos E.C. George Club Leafed Adenanthos NP 12 Adenanthos meisneri Lehm. 1a A 1 Adenanthos obovatus Labill. Basket Flower 1b A 1, 11, 22, 28 Adenanthos oreophilus E.C. Nelson 1a 33 Adenanthos pungens ssp. effussus Spiky Adenanthos NP R 8 Adenanthos pungens ssp. pungens NP R 8 Adenanthos sericeus Labill. Woolly Bush 1a A 1 Agonis linearifolia (D.C.) Sweet Swamp Peppermint 1b 10 Agrostocrinum scabrum (R. Br) Baill. Bluegrass 1a 17 Allocasuarina fraseriana (Miq) L.A.S. Sheoak 1b A 1, 10, 22 Johnson Allocasuarina humilis (Otto & F. -
Vegetation and Flora of Blackboy Ridge Reserve, Shire of Chittering, Western Australia
Vegetation and Flora of Blackboy Ridge Reserve, Shire of Chittering, Western Australia Gregory Keighery and Bronwen Keighery August 2013 Department of Parks and Wildlife Western Australian Conservation Science Centre Locked Bag 104, Bentley Delivery Centre, Western Australia, 6983 Vegetation and Flora of Blackboy Ridge Reserve, Shire of Chittering, Western Australia By Gregory Keighery and Bronwen Keighery Department of Parks and Wildlife Western Australian Conservation Science Centre Locked Bag 104, Bentley Delivery Centre, Western Australia, 6983 This publication was prepared as a report for the Department of Parks and Wildlife and Shire of Chittering, initially part of a World Wildlife Bioblitz, held in the Reserve over 24 hours on October 23-24, 2010 at Blackboy Ridge Cover photograph: Wandoo woodland from quadrat BLACK 03, spring 2010. The Reserve is named for the Xanthorrhoea plants that are a feature of the Wandoo woodland understorey on the rises in the Reserve. This Xanthorrhoea is X. acanthostachya a relatively restricted species near its most northern location in the Reserve. The fire earlier in the year has resulted in the Xanthorrhoea plants flowering together. Other shrubs are either regrowing from seed or rootstocks and are currently at low density. Photographs © Bronwen Keighery. 2 SUMMARY Blackboy Ridge Reserve is a small 61 hectare reserve vested in the Shire of Chittering on the southern side of Chittering Road, about 20 kilometres south-east of Bindoon. Quadrat based survey work was performed in the Reserve on the 23rd October 2010 by a group of conservation volunteers as part of a Bioblitz in the Reserve organised by the World Wildlife Fund. -
Diet of Herbivorous Marsupials in a Eucalyptus Marginata Forest and Their Impact on the Understorey Vegetation
JournalJournal of theof the Royal Royal Society Society of Westernof Western Australia, Australia, 80(2), 80:47-54, October 1997 1997 Diet of herbivorous marsupials in a Eucalyptus marginata forest and their impact on the understorey vegetation K A Shepherd1, G W Wardell-Johnson2,3, W A Loneragan1 & D T Bell1 1Department of Botany, The University of Western Australia, Nedlands WA 6907: email [email protected] 2Manjimup Research Centre, Department of Conservation and Land Management, Brain Street, Manjimup WA 6258 3Current address: Botany Department, University of Namibia, Windhoek, Namibia: email [email protected] Received April 1996; accepted February 1997 Abstract Wire exclosures were established to exclude herbivores in remnant jarrah (Eucalyptus marginata) forest vegetation within the Perup Nature Reserve, south-western Australia, and were assessed after a 10 year period. Significantly higher plant cover values were recorded for a number of species protected from herbivory inside the exclosures compared to outside. Sub-shrubs and vines showed the greatest increase in vegetation cover within exclosures. Bossiaea ornata, Billardiera variifolia, Opercularia hispidula, Logania serpyllifolia and Tetrarrhena laevis were most favoured by herbivore exclusion in terms of relative abundance. Faecal analysis confirmed that plant species having the greatest decrease in cover outside wire exclosures were consumed by one or more of the five predominant marsupial herbivores of the Perup forest. Faecal material collected over three sampling periods during 1992 revealed a total of 42 different plant species. The largest of the herbivores, the western grey kangaroo (Macropus fuliginosus), consumed the greatest diversity of plants (32 species in total), while the black-gloved wallaby (Macropus irma) and the tammar wallaby (Macropus eugenii) grazed 21 and 25 different species, respectively. -
Vegetation and Flora of Exploration Licence 70/2407 Keysbrook Western Australia
VEGETATION AND FLORA OF EXPLORATION LICENCE 70/2407 KEYSBROOK WESTERN AUSTRALIA Prepared for: MBS Environmental 4 Cooke Street WEST PERTH 6005 Prepared by: Bennett Environmental Consulting Pty Ltd Sollya heterophylla PO Box 341 KALAMUNDA 6926 December 2004 Reviewed May 2006 CONTENTS 1. INTRODUCTION ................................................................................................................................ 1 1.1 Background ................................................................................................................................. 1 1.2 Vegetation ................................................................................................................................... 1 1.3 Wetlands...................................................................................................................................... 2 1.4 Soils............................................................................................................................................. 2 1.5 Previous Survey........................................................................................................................... 2 1.6 Scope of Works ........................................................................................................................... 2 2. METHODS .......................................................................................................................................... 2 3. RESULTS ............................................................................................................................................