Odontochilus Putaoensis (Cranichideae, Orchidaceae), A
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The Structure of the Perennial Growth of Disa Un/Flora Berg
THE STRUCTURE OF THE PERENNIAL GROWTH OF DISA UN/FLORA BERG. ( ORCHIDACEAE) HONOURS SYSTEMATICS PROJECT JANET THOMAS OCTOBER 1990 SUPERVISOR: DR . .H.P. LINDER University of Cape Town The copyright of this thesis vests in the author. No quotation from it or information derived from it is to be published without full acknowledgement of the source. The thesis is to be used for private study or non- commercial research purposes only. Published by the University of Cape Town (UCT) in terms of the non-exclusive license granted to UCT by the author. University of Cape Town BOLUS LIBRARY 1 ABSTRACT The perennation of orchids is poorly understood, in particular that of the Orchidoidae. The understanding of perennation in the Orchidoidae is important because the root-stem tuberoid .is used as the one character defining the Orchidoidae as a monophyletic group. The root-stem tuberoid has never been examined for variation before. This project focuses on perennial growth in the Diseae in order to study the structbre and function of the root stem tuberoid in relation tp other organs and to contribute to the understanding of Orchidoid phylogeny. , INTRODUCTION Host te1perate monocotyledons have evolved underground resting or perennating organs for the climatically unfavourable season (Holttum 1955). A period of underground existence may allow a plant to escape unfavourable conditions, to counter environmental uncertainty, and to build reserves for flowering episodes (Calvo 1990). This is especially evident in the temperate members of the Orchidaceae and is made possible through sympodial growth· (Withnerj1974). Not .all temperate orchids have a resting period although they do have sympodial growth and do perennate. -
Nature Conservation (Wildlife) Regulation 2006
Queensland Nature Conservation Act 1992 Nature Conservation (Wildlife) Regulation 2006 Current as at 1 September 2017 Queensland Nature Conservation (Wildlife) Regulation 2006 Contents Page Part 1 Preliminary 1 Short title . 5 2 Commencement . 5 3 Purpose . 5 4 Definitions . 6 5 Scientific names . 6 Part 2 Classes of native wildlife and declared management intent for the wildlife Division 1 Extinct in the wild wildlife 6 Native wildlife that is extinct in the wild wildlife . 7 7 Declared management intent for extinct in the wild wildlife . 8 8 Significance of extinct in the wild wildlife to nature and its value 8 9 Proposed management intent for extinct in the wild wildlife . 8 10 Principles for the taking, keeping or use of extinct in the wild wildlife 9 Division 2 Endangered wildlife 11 Native wildlife that is endangered wildlife . 10 12 Declared management intent for endangered wildlife . 10 13 Significance of endangered wildlife to nature and its value . 10 14 Proposed management intent for endangered wildlife . 11 15 Principles for the taking, keeping or use of endangered wildlife . 12 Division 3 Vulnerable wildlife 16 Native wildlife that is vulnerable wildlife . 13 17 Declared management intent for vulnerable wildlife . 13 18 Significance of vulnerable wildlife to nature and its value . 13 19 Proposed management intent for vulnerable wildlife . 14 20 Principles for the taking, keeping or use of vulnerable wildlife . 15 Nature Conservation (Wildlife) Regulation 2006 Contents Division 4 Near threatened wildlife 26 Native wildlife that is near threatened wildlife . 16 27 Declared management intent for near threatened wildlife . 16 28 Significance of near threatened wildlife to nature and its value . -
Phylogenetic Relationships of Rhizoctonia Fungi Within the Cantharellales
fungal biology 120 (2016) 603e619 journal homepage: www.elsevier.com/locate/funbio Phylogenetic relationships of Rhizoctonia fungi within the Cantharellales Dolores GONZALEZa,*, Marianela RODRIGUEZ-CARRESb, Teun BOEKHOUTc, Joost STALPERSc, Eiko E. KURAMAEd, Andreia K. NAKATANIe, Rytas VILGALYSf, Marc A. CUBETAb aInstituto de Ecologıa, A.C., Red de Biodiversidad y Sistematica, Carretera Antigua a Coatepec No. 351, El Haya, 91070 Xalapa, Veracruz, Mexico bDepartment of Plant Pathology, North Carolina State University, Center for Integrated Fungal Research, Campus Box 7251, Raleigh, NC 27695, USA cCBS Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands dDepartment of Microbial Ecology, Netherlands Institute of Ecology (NIOO/KNAW), Droevendaalsesteeg 10, 6708 PB Wageningen, The Netherlands eUNESP, Faculdade de Ci^encias Agronomicas,^ CP 237, 18603-970 Botucatu, SP, Brazil fDepartment of Biology, Duke University, Durham, NC 27708, USA article info abstract Article history: Phylogenetic relationships of Rhizoctonia fungi within the order Cantharellales were studied Received 2 January 2015 using sequence data from portions of the ribosomal DNA cluster regions ITS-LSU, rpb2, tef1, Received in revised form and atp6 for 50 taxa, and public sequence data from the rpb2 locus for 165 taxa. Data sets 1 January 2016 were analysed individually and combined using Maximum Parsimony, Maximum Likeli- Accepted 19 January 2016 hood, and Bayesian Phylogenetic Inference methods. All analyses supported the mono- Available online 29 January 2016 phyly of the family Ceratobasidiaceae, which comprises the genera Ceratobasidium and Corresponding Editor: Thanatephorus. Multi-locus analysis revealed 10 well-supported monophyletic groups that Joseph W. Spatafora were consistent with previous separation into anastomosis groups based on hyphal fusion criteria. -
Orchids: 2017 Global Ex Situ Collections Assessment
Orchids: 2017 Global Ex situ Collections Assessment Botanic gardens collectively maintain one-third of Earth's plant diversity. Through their conservation, education, horticulture, and research activities, botanic gardens inspire millions of people each year about the importance of plants. Ophrys apifera (Bernard DuPon) Angraecum conchoglossum With one in five species facing extinction due to threats such (Scott Zona) as habitat loss, climate change, and invasive species, botanic garden ex situ collections serve a central purpose in preventing the loss of species and essential genetic diversity. To support the Global Strategy for Plant Conservation, botanic gardens create integrated conservation programs that utilize diverse partners and innovative techniques. As genetically diverse collections are developed, our collective global safety net against plant extinction is strengthened. Country-level distribution of orchids around the world (map data courtesy of Michael Harrington via ArcGIS) Left to right: Renanthera monachica (Dalton Holland Baptista ), Platanthera ciliaris (Wikimedia Commons Jhapeman) , Anacamptis boryi (Hans Stieglitz) and Paphiopedilum exul (Wikimedia Commons Orchi ). Orchids The diversity, stunning flowers, seductiveness, size, and ability to hybridize are all traits which make orchids extremely valuable Orchids (Orchidaceae) make up one of the largest plant families to collectors, florists, and horticulturists around the world. on Earth, comprising over 25,000 species and around 8% of all Over-collection of wild plants is a major cause of species flowering plants (Koopowitz, 2001). Orchids naturally occur on decline in the wild. Orchids are also very sensitive to nearly all continents and ecosystems on Earth, with high environmental changes, and increasing habitat loss and diversity found in tropical and subtropical regions. -
How to Cite Complete Issue More Information About This Article Journal's Webpage in Redalyc.Org Scientific Information System Re
Lankesteriana ISSN: 1409-3871 Lankester Botanical Garden, University of Costa Rica Pedersen, Henrik Æ.; Find, Jens i.; Petersen, Gitte; seberG, Ole On the “seidenfaden collection” and the multiple roles botanical gardens can play in orchid conservation Lankesteriana, vol. 18, no. 1, 2018, January-April, pp. 1-12 Lankester Botanical Garden, University of Costa Rica DOI: 10.15517/lank.v18i1.32587 Available in: http://www.redalyc.org/articulo.oa?id=44355536001 How to cite Complete issue Scientific Information System Redalyc More information about this article Network of Scientific Journals from Latin America and the Caribbean, Spain and Journal's webpage in redalyc.org Portugal Project academic non-profit, developed under the open access initiative LANKESTERIANA 18(1): 1–12. 2018. doi: http://dx.doi.org/10.15517/lank.v18i1.32587 ON THE “SEIDENFADEN COLLECTION” AND THE MULTIPLE ROLES BOTANICAL GARDENS CAN PLAY IN ORCHID CONSERVATION HENRIK Æ. PEDERSEN1,3, JENS I. FIND2,†, GITTE PETERSEN1 & OLE SEBERG1 1 Natural History Museum of Denmark, University of Copenhagen, Øster Voldgade 5–7, DK-1353 Copenhagen K, Denmark 2 Department of Geosciences and Natural Resource Management, University of Copenhagen, Rolighedsvej 23, DK-1958 Frederiksberg C, Denmark 3 Author for correspondence: [email protected] † Deceased 2nd December 2016 ABSTRACT. Using the “Seidenfaden collection” in Copenhagen as an example, we address the common view that botanical garden collections of orchids are important for conservation. Seidenfaden collected live orchids all over Thailand from 1957 to 1983 and created a traditional collection for taxonomic research, characterized by high taxonomic diversity and low intraspecific variation. Following an extended period of partial neglect, we managed to set up a five-year project aimed at expanding the collection with a continued focus on taxonomic diversity, but widening the geographic scope to tropical Asia. -
Fungal Diversity Driven by Bark Features Affects Phorophyte
www.nature.com/scientificreports OPEN Fungal diversity driven by bark features afects phorophyte preference in epiphytic orchids from southern China Lorenzo Pecoraro1*, Hanne N. Rasmussen2, Sofa I. F. Gomes3, Xiao Wang1, Vincent S. F. T. Merckx3, Lei Cai4 & Finn N. Rasmussen5 Epiphytic orchids exhibit varying degrees of phorophyte tree specifcity. We performed a pilot study to investigate why epiphytic orchids prefer or avoid certain trees. We selected two orchid species, Panisea unifora and Bulbophyllum odoratissimum co-occurring in a forest habitat in southern China, where they showed a specifc association with Quercus yiwuensis and Pistacia weinmannifolia trees, respectively. We analysed a number of environmental factors potentially infuencing the relationship between orchids and trees. Diference in bark features, such as water holding capacity and pH were recorded between Q. yiwuensis and P. weinmannifolia, which could infuence both orchid seed germination and fungal diversity on the two phorophytes. Morphological and molecular culture-based methods, combined with metabarcoding analyses, were used to assess fungal communities associated with studied orchids and trees. A total of 162 fungal species in 74 genera were isolated from bark samples. Only two genera, Acremonium and Verticillium, were shared by the two phorophyte species. Metabarcoding analysis confrmed the presence of signifcantly diferent fungal communities on the investigated tree and orchid species, with considerable similarity between each orchid species and its host tree, suggesting that the orchid-host tree association is infuenced by the fungal communities of the host tree bark. Epiphytism is one of the most common examples of commensalism occurring in terrestrial environments, which provides advantages, such as less competition and increased access to light, protection from terrestrial herbivores, and better fower exposure to pollinators and seed dispersal 1,2. -
Seidenfaden Malaysia: 0.65 These Figures Are Surprisingly High, They Apply to Single Only. T
BIOGEOGRAPHY OF MALESIAN ORCHIDACEAE 273 VIII. Biogeographyof Malesian Orchidaceae A. Schuiteman Rijksherbarium/Hortus Botanicus, P.O. Box 9514, 2300 RA Leiden, The Netherlands INTRODUCTION The Orchidaceae outnumber far other in Malesia. At how- by any plant family present, accurate estimate of the of Malesian orchid is difficult to make. ever, an number species Subtracting the numberofestablishedsynonyms from the numberof names attributed to Malesian orchid species results in the staggering figure of 6414 species, with a retention of 0.74. This is ratio (ratio of ‘accepted’ species to heterotypic names) undoubtedly a overestimate, of the 209 Malesian orchid have been revised gross as most genera never their entire from availablerevisions estimate realis- over range. Extrapolating to a more tic retention ratio is problematic due to the small number of modern revisions and the different of treated. If look for Malesian of nature the groups we comparison at species wide ofretention ratios: some recently revised groups, we encounter a range Bulbophylluw sect. Uncifera (Vermeulen, 1993): 0.24 Dendrobium sect. Oxyglossum (Reeve & Woods, 1989): 0.24 Mediocalcar (Schuiteman, 1997): 0.29 Pholidota (De Vogel, 1988): 0.29 Bulbophyllum sect. Pelma (Vermeulen, 1993): 0.50 Paphiopedilum (Cribb, 1987, modified): 0.57 Dendrobium sect. Spatulata (Cribb, 1986, modified): 0.60. Correspondingly, we find a wide rangeof estimates for the ‘real’ numberof known Male- sian orchid species: from 2050 to 5125. Another approach would be to look at a single area, and to compute the retention ratio for the orchid flora of that area. If we do this for Java (mainly based on Comber, 1990), Peninsular Malaysia & Singapore (Seidenfaden & Wood, 1992) and Sumatra (J.J. -
Cranichideae; Orchidaceae)
Phytotaxa 202 (3): 207–213 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2015 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.202.3.4 Morphological comparisons of two pairs of easily confused species in subtribe Goodyerinae (Cranichideae; Orchidaceae) QIAO-XIAO LIU1, ZHI-QUAN CHENG1, HONG-YUN TAN2, TIAN-CHUAN HSU3 & HUAI-ZHEN TIAN1* 1School of Life Sciences, East China Normal University, Shanghai 200241, China; E-mail: [email protected] 2Key Laboratory of Tropical Forest Ecology, Key Laboratory of Tropical Plant Resource and Sustainable Use, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Yunnan 666303, China 3Institute of Molecular & Cellular Biology, National Tsing Hua University, Hsinchu 30013, Taiwan, China Abstract Two yellow-lipped species of Zeuxine viz. Z. flava and Z. sakagutii and another pair of species of Rhomboda, R. moulmei- nensis and R. fanjingensis, are so similar that they are frequently misidentified. In this paper, based on field observations, study of type specimens and protologues, illustrations and comparisons of these two pairs of confused species are provided to enable identification. Key words: Chinese orchids, Rhomboda, Zeuxine Introduction Zeuxine Lindley (1826: 18) and Rhomboda Lindley (1857: 181) belong to subtribe Goodyerinae (Orchidoideae; Cranichideae; Pridgeon et al. 2003a, 2003b). Zeuxine comprises about 80 species distributed in tropical and southern Africa through tropical and subtropical Asia, to New Guinea, northeastern Australia, and the southwestern Pacific islands; with 14 species occurring in China, two of them are endemic (Chen et al. 2009b). Flowers of Zeuxine species are nearly always white or green, but a few are yellow. -
Orchids of Suspa-Kshamawoti, Dolakha -An Annotated Checklist
Banko Janakari, Vol 29 No. 2, 2019 Pp 28‒41 Karki & Ghimire https://doi.org:10.3126/banko.v29i2.28097 Orchids of Suspa-Kshamawoti, Dolakha -An annotated checklist S. Karki1* and S. K. Ghimire1 Suspa-Kshamawoti area of Dolakha district covers diverse vegetation types and harbors many interesting species of orchids. This paper documents 69 species of orchids covering 33 genera based on repeated field surveys and herbarium collections. Of them, 50 species are epiphytic (including lithophytes) and 19 species are terrestrial. Information regarding habit and habitat, phenology, host species and elevational range of distribution of each species are provided in the checklist. Keywords : Bulbophyllum, Nepal, Orchidaceae rchids are one of the most diverse and contributions on documentation of orchid flora are highly evolved groups of flowering made by Bajracharya (2001; 2004); Rajbhandari Oplants, and orchidaceae is the largest and Bhattrai (2001); Bajracharya and Shrestha family comprising 29,199 species and are (2003); Rajbhandari and Dahal (2004); Milleville globally distributed (Govaerts et al., 2017). Out and Shrestha (2004); Subedi et al. (2011); of them, two-third belong to epiphytes (Zotz and Rajbhandari (2015); Raskoti (2015); Raskoti and Winkler, 2013). In Nepal, orchidaceae is one of Ale (2009; 2011; 2012; 2019) and Bhandari et al. the major families amongst the higher flowering (2016 b; 2019). Suspa-Kshamawoti, the northern plants and comprises 502 taxa belonging to 108 part of the Dolakha district covers diverse genera, which forms around 8 percent of our flora vegetation and harbors some interesting species (Raskoti and Ale, 2019). The number of species of orchids. Bhandari et al. -
Supplementary Material Saving Rainforests in the South Pacific
Australian Journal of Botany 65, 609–624 © CSIRO 2017 http://dx.doi.org/10.1071/BT17096_AC Supplementary material Saving rainforests in the South Pacific: challenges in ex situ conservation Karen D. SommervilleA,H, Bronwyn ClarkeB, Gunnar KeppelC,D, Craig McGillE, Zoe-Joy NewbyA, Sarah V. WyseF, Shelley A. JamesG and Catherine A. OffordA AThe Australian PlantBank, The Royal Botanic Gardens and Domain Trust, Mount Annan, NSW 2567, Australia. BThe Australian Tree Seed Centre, CSIRO, Canberra, ACT 2601, Australia. CSchool of Natural and Built Environments, University of South Australia, Adelaide, SA 5001, Australia DBiodiversity, Macroecology and Conservation Biogeography Group, Faculty of Forest Sciences, University of Göttingen, Büsgenweg 1, 37077 Göttingen, Germany. EInstitute of Agriculture and Environment, Massey University, Private Bag 11 222 Palmerston North 4474, New Zealand. FRoyal Botanic Gardens, Kew, Wakehurst Place, RH17 6TN, United Kingdom. GNational Herbarium of New South Wales, The Royal Botanic Gardens and Domain Trust, Sydney, NSW 2000, Australia. HCorresponding author. Email: [email protected] Table S1 (below) comprises a list of seed producing genera occurring in rainforest in Australia and various island groups in the South Pacific, along with any available information on the seed storage behaviour of species in those genera. Note that the list of genera is not exhaustive and the absence of a genus from a particular island group simply means that no reference was found to its occurrence in rainforest habitat in the references used (i.e. the genus may still be present in rainforest or may occur in that locality in other habitats). As the definition of rainforest can vary considerably among localities, for the purpose of this paper we considered rainforests to be terrestrial forest communities, composed largely of evergreen species, with a tree canopy that is closed for either the entire year or during the wet season. -
A Literature Review of Corybas Rivularis (A.Cunn.) Rchb.F.; the Natural History, Taxonomy and Ecology
http://researchcommons.waikato.ac.nz/ Research Commons at the University of Waikato Copyright Statement: The digital copy of this thesis is protected by the Copyright Act 1994 (New Zealand). The thesis may be consulted by you, provided you comply with the provisions of the Act and the following conditions of use: Any use you make of these documents or images must be for research or private study purposes only, and you may not make them available to any other person. Authors control the copyright of their thesis. 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. A Taxonomic Review of Corybas rivularis (Orchidaceae) – Inferred from Molecular and Morphological Analyses A thesis submitted in partial fulfilment of the requirements for the degree of Master of Science in Biological Sciences at The University of Waikato by Abraham John Coffin 2016 Drawings of Corybas rivularis (top), C. “kaimai” (middle) and C. “whiskers” (bottom). Illustrated by Abraham Coffin. Abstract This research has expanded the level of precision utilised in critically examining the morphology of Corybas rivularis Rchb.f (Orchidaceae), related species and undescribed populations. Corybas rivularis and related species have undergone taxonomic revisions, incorporating errors that took decades to discover. Utilising morphological and molecular analyses has provided insights into this problematic group. A new protocol for examining the morphological characteristics of C. rivularis has been developed, based on concepts of floral morphometrics, to determine the level of morphological variation within the species, closely related species and a range of undescribed populations, some of which have tag-names. -
Dating the Origin of the Orchidaceae from a Fossil Orchid with Its Pollinator
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/6111228 Dating the origin of the Orchidaceae from a fossil orchid with its pollinator Article in Nature · September 2007 DOI: 10.1038/nature06039 · Source: PubMed CITATIONS READS 211 770 5 authors, including: Santiago R Ramírez Barbara Gravendeel University of California, Davis Leiden University, Naturalis Biodiversity Center & University of Applied Sciences L… 50 PUBLICATIONS 999 CITATIONS 208 PUBLICATIONS 2,081 CITATIONS SEE PROFILE SEE PROFILE Rodrigo B. Singer Naomi E Pierce Universidade Federal do Rio Grande do Sul Harvard University 109 PUBLICATIONS 1,381 CITATIONS 555 PUBLICATIONS 6,496 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Insect endosymbiont diversity View project Support threatened research Institutions from Southern Brazil (Rio Grande do Sul) View project All content following this page was uploaded by Barbara Gravendeel on 31 May 2014. The user has requested enhancement of the downloaded file. Vol 448 | 30 August 2007 | doi:10.1038/nature06039 LETTERS Dating the origin of the Orchidaceae from a fossil orchid with its pollinator Santiago R. Ramı´rez1, Barbara Gravendeel2, Rodrigo B. Singer3, Charles R. Marshall1,4 & Naomi E. Pierce1 Since the time of Darwin1, evolutionary biologists have been fas- subfamily showed that the size, shape and ornamentation of the cinated by the spectacular adaptations to insect pollination exhib- fossil closely resemble those of modern members of the subtribe ited by orchids. However, despite being the most diverse plant Goodyerinae, particularly the genera Kreodanthus and Microchilus family on Earth2, the Orchidaceae lack a definitive fossil record (Supplementary Table 1).