(Hemiptera: Aleyrodidae) from Protea Nitida in South Africa
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Pathogens Associated with Diseases. of Protea, Leucospermum and Leucadendron Spp
PATHOGENS ASSOCIATED WITH DISEASES. OF PROTEA, LEUCOSPERMUM AND LEUCADENDRON SPP. Lizeth Swart Thesis presented in partial fulfillment of the requirements for the degree of Master of Science in Agriculture at the University of Stellenbosch Supervisor: Prof. P. W. Crous Decem ber 1999 Stellenbosch University https://scholar.sun.ac.za DECLARATION 1, the undersigned, hereby declare that the work contained in this thesis is my own original work and has not previously in its entirety or in part been submitted at any university for a degree. SIGNATURE: DATE: Stellenbosch University https://scholar.sun.ac.za PATHOGENS ASSOCIATED WITH DISEASES OF PROTEA, LEUCOSPERMUM ANDLEUCADENDRONSPP. SUMMARY The manuscript consists of six chapters that represent research on different diseases and records of new diseases of the Proteaceae world-wide. The fungal descriptions presented in this thesis are not effectively published, and will thus be formally published elsewhere in scientific journals. Chapter one is a review that gives a detailed description of the major fungal pathogens of the genera Protea, Leucospermum and Leucadendron, as reported up to 1996. The pathogens are grouped according to the diseases they cause on roots, leaves, stems and flowers, as well as the canker causing fungi. In chapter two, several new fungi occurring on leaves of Pro tea, Leucospermum, Telopea and Brabejum collected from South Africa, Australia or New Zealand are described. The following fungi are described: Cladophialophora proteae, Coniolhyrium nitidae, Coniothyrium proteae, Coniolhyrium leucospermi,Harknessia leucospermi, Septoria prolearum and Mycosphaerella telopeae spp. nov. Furthermore, two Phylloslicla spp., telopeae and owaniana are also redecribed. The taxonomy of the Eisinoe spp. -
These De Doctorat
Université d’Antananarivo Faculté des Sciences Département de Biochimie fondamentale et appliquée ------------------------------------------------------------------- THESE DE DOCTORAT en Sciences de la Vie - Spécialité : Biochimie Etudes chimique et biologique d’une plante médicinale malgache : Dilobeia thouarsii (PROTEACEAE) Présentée et soutenue publiquement par : RAVELOMANANA- RAZAFINTSALAMA Vahinalahaja Eliane Titulaire de DEA Biochimie appliquée aux sciences médicales Le 02 février 2012 Composition du jury : Président : ANDRIANARISOA Blandine, Professeur titulaire Rapporteur interne : RAZANAMPARANY Julia Louisette, Professeur titulaire Rapporteur externe : RAMANOELINA Panja, Professeur titulaire Examinateur : RAZAFIMAHEFA-RAMILISON Reine Dorothée, Professeur titulaire Directeurs de thèse : JEANNODA Victor, Professeur titulaire MAMBU Lengo, Maître de Conférences HDR Remerciements Dédicaces Je dédie ce travail de thèse à mes proches: A mon mari Rado, et à mon fils Randhy, source d’amour et de tendresse, qui n’ont jamais cessé de croire en moi. Ma plus profonde reconnaissance va à vous, pour votre irremplaçable et inconditionnel soutien tout au long de ces années de travail. Merci d’avoir partagé avec moi les hauts et les bas de ces années de thèse, merci pour vos encouragements quotidiens et vos prières. Sans vous, cette thèse n’aurait jamais vu le jour. A Dada et Neny, qui ont toujours été là pour moi, m’ont donné sans compter tous les moyens pour réussir, pour leurs sacrifices et leurs prières incessantes. Merci de m’avoir toujours soutenue et de m’avoir aidée à surmonter toutes les difficultés rencontrées au cours de cette thèse. A ma belle‐mère, Neny, qui m’a beaucoup aidée et encouragée durant mes séjours à l’étranger. Merci pour tes conseils et tes prières. -
Avian Pollinators and the Pollination Syndromes of Selected Mountain Fynbos Plants
Avian pollinators and the pollination syndromes of selected Mountain Fynbos plants A.G. Rebelo, W.R. Siegfried and A.A. Crowe FitzPatrick Institute, University of Cape Town, Rondebosch The flowering phenology of Erica and proteaceous plants and Introduction the abundance of nectarivorous birds were monitored in Mountain fynbos is a major vegetation type in the fynbos Mountain Fynbos in the Jonkershoek State Forest, South Africa. Species tended to flower for short periods in summer biome (Kruger 1979) which corresponds geographically at high altitudes, or for longer periods in autumn and winter with the 'Capensis' region, delineated by Werger (1978) as at low altitudes. Three avian species apparently tracked the one of the plant biogeographical regions of southern Africa. flowers occurring at low altitudes during winter and, when The structural character of fynbos vegetation is largely present. at high altitudes during summer. Statistical analyses determined by three families, Restionaceae, Proteaceae and confirmed that the distribution of Promerops cafer is primarily Ericaceae, and the flora is notable for its great richness in correlated with the abundance of protea flowers, and that of species (Taylor 1979) . Nectarinia vio/acea with Erica flowers. The evolution of an Nearly all members of the Restionaceae are dioecious, unusually high ratio of putative avian pollinators to wind-pollinated graminoids (Pillans 1928) , whereas the ornithophilous plant species in Mountain Fynbos is discussed. Ericaceae and Proteaceae display more diverse pollination S. Afr. J. Bot. 1984, 3: 285-296 syndromes with a high proportion of putative bird-pollinated Die bloeifenologie van Erica en proteaplante en die talrykheid species (Baker & Oliver 1967; Rourke 1980, pers. -
Literaturverzeichnis
Literaturverzeichnis Abaimov, A.P., 2010: Geographical Distribution and Ackerly, D.D., 2009: Evolution, origin and age of Genetics of Siberian Larch Species. In Osawa, A., line ages in the Californian and Mediterranean flo- Zyryanova, O.A., Matsuura, Y., Kajimoto, T. & ras. Journal of Biogeography 36, 1221–1233. Wein, R.W. (eds.), Permafrost Ecosystems. Sibe- Acocks, J.P.H., 1988: Veld Types of South Africa. 3rd rian Larch Forests. Ecological Studies 209, 41–58. Edition. Botanical Research Institute, Pretoria, Abbadie, L., Gignoux, J., Le Roux, X. & Lepage, M. 146 pp. (eds.), 2006: Lamto. Structure, Functioning, and Adam, P., 1990: Saltmarsh Ecology. Cambridge Uni- Dynamics of a Savanna Ecosystem. Ecological Stu- versity Press. Cambridge, 461 pp. dies 179, 415 pp. Adam, P., 1994: Australian Rainforests. Oxford Bio- Abbott, R.J. & Brochmann, C., 2003: History and geography Series No. 6 (Oxford University Press), evolution of the arctic flora: in the footsteps of Eric 308 pp. Hultén. Molecular Ecology 12, 299–313. Adam, P., 1994: Saltmarsh and mangrove. In Groves, Abbott, R.J. & Comes, H.P., 2004: Evolution in the R.H. (ed.), Australian Vegetation. 2nd Edition. Arctic: a phylogeographic analysis of the circu- Cambridge University Press, Melbourne, pp. marctic plant Saxifraga oppositifolia (Purple Saxi- 395–435. frage). New Phytologist 161, 211–224. Adame, M.F., Neil, D., Wright, S.F. & Lovelock, C.E., Abbott, R.J., Chapman, H.M., Crawford, R.M.M. & 2010: Sedimentation within and among mangrove Forbes, D.G., 1995: Molecular diversity and deri- forests along a gradient of geomorphological set- vations of populations of Silene acaulis and Saxi- tings. -
Kirstenbosch NBG List of Plants That Provide Food for Honey Bees
Indigenous South African Plants that Provide Food for Honey Bees Honey bees feed on nectar (carbohydrates) and pollen (protein) from a wide variety of flowering plants. While the honey bee forages for nectar and pollen, it transfers pollen from one flower to another, providing the service of pollination, which allows the plant to reproduce. However, bees don’t pollinate all flowers that they visit. This list is based on observations of bees visiting flowers in Kirstenbosch National Botanical Garden, and on a variety of references, in particular the following: Plant of the Week articles on www.PlantZAfrica.com Johannsmeier, M.F. 2005. Beeplants of the South-Western Cape, Nectar and pollen sources of honeybees (revised and expanded). Plant Protection Research Institute Handbook No. 17. Agricultural Research Council, Plant Protection Research Institute, Pretoria, South Africa This list is primarily Western Cape, but does have application elsewhere. When planting, check with a local nursery for subspecies or varieties that occur locally to prevent inappropriate hybridisations with natural veld species in your vicinity. Annuals Gazania spp. Scabiosa columbaria Arctotis fastuosa Geranium drakensbergensis Scabiosa drakensbergensis Arctotis hirsuta Geranium incanum Scabiosa incisa Arctotis venusta Geranium multisectum Selago corymbosa Carpanthea pomeridiana Geranium sanguineum Selago canescens Ceratotheca triloba (& Helichrysum argyrophyllum Selago villicaulis ‘Purple Turtle’ carpenter bees) Helichrysum cymosum Senecio glastifolius Dimorphotheca -
Fungal Pathogens of Proteaceae
Persoonia 27, 2011: 20–45 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158511X606239 Fungal pathogens of Proteaceae P.W. Crous 1,3,8, B.A. Summerell 2, L. Swart 3, S. Denman 4, J.E. Taylor 5, C.M. Bezuidenhout 6, M.E. Palm7, S. Marincowitz 8, J.Z. Groenewald1 Key words Abstract Species of Leucadendron, Leucospermum and Protea (Proteaceae) are in high demand for the interna- tional floriculture market due to their brightly coloured and textured flowers or bracts. Fungal pathogens, however, biodiversity create a serious problem in cultivating flawless blooms. The aim of the present study was to characterise several cut-flower industry of these pathogens using morphology, culture characteristics, and DNA sequence data of the rRNA-ITS and LSU fungal pathogens genes. In some cases additional genes such as TEF 1- and CHS were also sequenced. Based on the results of ITS α this study, several novel species and genera are described. Brunneosphaerella leaf blight is shown to be caused by LSU three species, namely B. jonkershoekensis on Protea repens, B. nitidae sp. nov. on Protea nitida and B. protearum phylogeny on a wide host range of Protea spp. (South Africa). Coniothyrium-like species associated with Coniothyrium leaf systematics spot are allocated to other genera, namely Curreya grandicipis on Protea grandiceps, and Microsphaeropsis proteae on P. nitida (South Africa). Diaporthe leucospermi is described on Leucospermum sp. (Australia), and Diplodina microsperma newly reported on Protea sp. (New Zealand). Pyrenophora blight is caused by a novel species, Pyrenophora leucospermi, and not Drechslera biseptata or D. -
The Influence of Pollinators and Seed Predation on Seed Production in Dwarf Grassland Protea
CORE Metadata, citation and similar papers at core.ac.uk Provided by Elsevier - Publisher Connector Available online at www.sciencedirect.com South African Journal of Botany 79 (2012) 77–83 www.elsevier.com/locate/sajb The influence of pollinators and seed predation on seed production in dwarf grassland Protea “sugarbushes” (Proteaceae) ⁎ S.-L. Steenhuisen , S.D. Johnson School of Life Sciences, University of KwaZulu-Natal Pietermaritzburg, Private Bag X01, Scottsville 3209, South Africa Received 8 November 2011; received in revised form 25 November 2011; accepted 5 December 2011 Abstract Flowers of many plant species are visited by both birds and insects, making it necessary to establish their relative contributions to seed set. In Protea, available evidence points to an overwhelming preponderance of bird-pollination systems in the genus, but the scented flowers of several dwarf grassland “sugarbush” species suggest that some Protea species may be adapted for insect pollination. In this study, we used both selective exclusion of vertebrates and complete exclusion of all visitors to investigate whether the insects that visit the scented flowerheads of three Protea species (Protea dracomontana, Protea simplex and Protea welwitschii) in KwaZulu-Natal, South Africa contribute to seed production. We also performed supplemental hand pollinations to test for pollen limitation. Seed set was generally higher in inflorescences subjected to vertebrate exclusion than in those from which all visitors were excluded, suggesting that fertile cross-pollen was deposited by insects, but these differences were slight because of high levels of self-fertilization in the study species. Pollen deposition and pollen tube growth were similar for vertebrate- excluded and open-pollinated inflorescences. -
Protea Glabra Thunb
Protea glabra Thunb. Clanwilliam Sugarbush Kaiingsuikerbos Other Common Names: Brownsel Sugarbush, Age to first flowering: First flowers recorded Chestnut Sugarbush, Scented Protea, at 1 years, 50% estimated at 2 years, and Bierbos, Kaiingbos, Kaiinghout, Kayang 100% recorded at 3 years. Sugarbush, Kreupelwaboom, 1 Krukkelwaboom, Kruppelwaboom. g in Other Scientific Names: banksii Kotzsch ex er w Meisn, buekiana Meisn, pyrifolia Buek ex 0.5 Meisn, thunbergii (Endl). s flo % Site 1094 Records 0 0123456789101112 Population (1088 records): 21% Common, Age (Years after fire) 59% Frequent, 20% Rare. Height (1076 records): 6% 0.2-1 m tall, 45% 1- Dispersion (984 records): 67% variable, 2 m tall, 48% 2-5 m tall, 1% taller than 5 m. 31% clumped, 1% widespread. Pollinators (58 records): 74% beetles, Flowering (1058 records with: Jan 43, Feb 33, 10% birds, 10% bees or wasps, 3% flies, Mar 103, Apr 89, May 39, Jun 116, Jul 93, 2% butterflies or moths. Aug 145, Sep 149, Oct 174, Nov 59, Dec Detailed Pollinators (17 records): Monkey 15): Buds from Mar to Aug ; Flowering from Beetle (4), Southern Double-collared Jun to Sep 32; Peak Flowering from not Sunbird (2), Malachite Sunbird (2), Honey significant; Over from Sep to Nov; Fruit Bee (2), Green Stripy Beetle (2), Great from Sep to May; Nothing from Mar to Apr Protea Beetle (2), Orange-breasted Sunbird, and Dec. Peak levels at 91% in Aug. Green Monkey Beetle, Green Beetle. Historically recorded as flowering from Jul to Nov, principally Aug to Sep. Habitat: 2320 Distance to Ocean (1078 Altitude (m) records): 100% inland - 2120 further than 2 km from 1920 coast. -
Proteas with Altitude Report 2016
proteas With Altitude Annual report 2016 Robbie Blackhall-Miles and Ben Ram Abstract This report aims to show how the ‘proteas With Altitude’ project has progressed over the past 12 months. It is an opportunity to review the process of setting up the nursery site, analyse data gathered about the species grown and set aims for the year ahead. Background In 2015, the RHS, Scottish Rock Garden Club, Stellenbosch University Botanical Gardens and the Western Cape Nature Conservation Board (Cape Nature), supported an expedition to study the habitat and growing conditions, as well as to collect seed, of the high altitude Proteaceae in the Western Cape of South Africa. The expedition collected seed of 31 species as the first stage in a long- term project attempting to gain information on the horticultural requirements of these species from germination through to maturity, to inform future ex-situ conservation through garden cultivation. Nursery Setup Having secured the long-term rental of a small area of land within a secure compound, a research nursery has been set up, to study the horticultural requirements of the species collected in South Africa. The nursery also includes propagation facilities for the NCCPG (Plant Heritage) National Collection of South Eastern Australian Banksia Species, as well as a site for the cultivation of several internationally threatened species. The site was levelled, using additional aggregates where necessary. A ‘Mypex’ weed-proof membrane was laid and a wire fence provides protection against browsing by rabbits. Water and Electricity still need to be installed but the main infrastructure is in place and functioning as intended. -
Ecology and Systematics of South African Protea- Associated Ophiostoma Species
ECOLOGY AND SYSTEMATICS OF SOUTH AFRICAN PROTEA- ASSOCIATED OPHIOSTOMA SPECIES FRANCOIS ROETS Dissertation presented for the degree of Doctor of Philosophy at Stellenbosch University Promotors: Doctor L.L. Dreyer, Professor P.W. Crous and Professor M.J. Wingfield July 2006 DECLARATION I, the undersigned, hereby declare that the work contained in this thesis is my own original work and has not previously in its entirety or part been submitted at any university for a degree. ………………………. ………………………. F. Roets Date "Life did not take over the globe by combat, but by networking" (Margulis and Sagan 1986) SUMMARY The well-known, and often phytopathogenic, ophiostomatoid fungi are represented in South Africa by the two phylogenetically distantly related genera Ophiostoma (Ophiostomatales) and Gondwanamyces (Microascales). They are commonly associated with the fruiting structures (infructescences) of serotinous members of the African endemic plant genus Protea. The species O. splendens, O. africanum, O. protearum, G. proteae and G. capensis have been collected from various Protea spp. in South Africa where, like other ophiostomatoid fungi, they are thought to be transported by arthropod vectors. The present study set out to identify the vector organisms of Protea-associated members of mainly Ophiostoma species, using both molecular and direct isolation methods. A polymerase chain reaction (PCR) and taxon specific primers for the two Protea-associated ophiostomatoid genera were developed. Implementation of these newly developed methods revealed the presence of Ophiostoma and Gondwanamyces DNA on three insect species. They included a beetle (Genuchus hottentottus), a bug (Oxycarenus maculates) and a psocopteran species. It was, however, curious that the frequency of these insects that tested positive for ophiostomatoid DNA was very low, despite the fact that ophiostomatoid fungi are known to colonise more than 50% of Protea infructescences. -
Temperature Controls Phenology in Continuously Flowering Protea Species of Subtropical Africa
APPLICATION ARTICLE INVITED SPECIAL ARTICLE For the Special Issue: Emerging Frontiers in Phenological Research Temperature controls phenology in continuously flowering Protea species of subtropical Africa Barnabas H. Daru1,5 , Matthew M. Kling2 , Emily K. Meineke3 , and Abraham E. van Wyk4 Manuscript received 1 October 2018; revision accepted 4 January PREMISE OF THE STUDY: Herbarium specimens are increasingly used as records of plant flow- 2019. ering phenology. However, most herbarium- based studies on plant phenology focus on taxa 1 Department of Life Sciences, Texas A&M University–Corpus from temperate regions. Here, we explore flowering phenologic responses to climate in the Christi, 6300 Ocean Drive, Corpus Christi, Texas 78412, USA subtropical plant genus Protea (Proteaceae), an iconic group of plants that flower year- round 2 Department of Integrative Biology, University of California, and are endemic to subtropical Africa. Berkeley, California 94720, USA 3 Department of Organismic and Evolutionary Biology, Harvard METHODS: We present a novel, circular sliding window approach to investigate phenological University Herbaria, 22 Divinity Avenue, Cambridge, patterns developed for species with year- round flowering. We employ our method to evalu- Massachusetts 02138, USA ate the extent to which site- to- site and year- to- year variation in temperature and precipita- 4 Department of Plant and Soil Sciences, University of Pretoria, tion affect flowering dates using a database of 1727 herbarium records of 25 Protea species. Pretoria 0083, South Africa We also explore phylogenetic conservatism in flowering phenology. 5 Author for correspondence: [email protected] Citation: Daru, B. H., M. M. Kling, E. K. Meineke, and A. E. van RESULTS: We show that herbarium data combined with our sliding window approach Wyk. -
Endophytes Isolated from Three Species of Protea in a Nature Reserve in the Western Cape, South Africa
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Sydowia Jahr/Year: 2001 Band/Volume: 53 Autor(en)/Author(s): Taylor Joanne E., Denman Sandra, Crous Pedro W. Artikel/Article: Endophytes isolated from three species of Protea in a nature reserve in the Western Cape, South Africa. 247-260 ©Verlag Ferdinand Berger & Söhne Ges.m.b.H., Horn, Austria, download unter www.biologiezentrum.at Endophytes isolated from three species of Protea in a nature reserve in the Western Cape, South Africa Joanne E. Taylor1, Sandra Denman & Pedro W. Crous Department of Plant Pathology, University of Stellenbosch, Private Bag XI, Stellenbosch 7602, South Africa Taylor, J. E., S. Denman & P. W. Crous (2001). Endophytes isolated from three species of Protea in a nature reserve in the Western Cape, South Africa. - Sydowia 53(2): 247-260. Healthy leaves of three species of Protea, P. nitida, P. re-pens and P. neriifolia, were tested for endophytic fungi. Nine plants of each Protea species were sampled from a natural site which is ecologically undisturbed, other than from periodic bush fires. Leaves were sampled from the current flush (young leaves) and the previous year's flush (old leaves). After surface sterilisation, tissue was excised from the midrib (vein) and the leaf tissue either side of the midrib (intervein), plated on agar and all fungal colonies that developed were identified. Simple correspondence analysis showed that Protea repens and P. neriifolia had similar fungal endophyte assemblages, which differed from that of P. nitida. Significant differences in the numbers of isolates obtained from the different hosts, tissue types and tissue ages were demonstrated.