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Rudolf Schlechter's South
LANKESTERIANA 21(2): 235–268. 2021. doi: http://dx.doi.org/10.15517/lank.v21i2.47977 RUDOLF SCHLECHTER’S SOUTH-AMERICAN ORCHIDS V. SCHLECHTER’S “NETWORK”: ECUADOR AND PERU CARLOS OSSENBACH1,2,4 & RUDOLF JENNY3 1Orquideario 25 de mayo, Sabanilla de Montes de Oca, San José, Costa Rica 2Jardín Botánico Lankester, Universidad de Costa Rica, Cartago, Costa Rica 3Jany Renz Herbarium, Swiss Orchid Foundation, Basel, Switzerland 4Corresponding author: [email protected] ABSTRACT. The fifth chapter of the series about Rudolf Schlechter’s South-American orchids introduces us to those botanists and orchid collectors who travelled and worked in Ecuador and Peru and supplied Schlechter with many of the new orchid species he described. As in previous chapters, the biographies and accomplishments of these travellers are preceded by brief geographical and historical outlines for each of these countries. It is worth mentioning that the lives and orchids of such prominent figures in the orchidology of South America as F.C. Lehmann, W. Hennis, E. Bungeroth and E. Ule, who collected in Ecuador and Peru, have already been mentioned in previous chapters and are therefore omitted here. KEYWORDS/PALABRAS CLAVE: biography, biografía, history of botany, historia de la botánica, Orchidaceae ECUADOR. Ecuador is divided geographically into three Over 1000 km west of the coast of Ecuador, we find continental regions: the lowlands along the Pacific coast the archipelago of the Galapagos, of volcanic origin. The known as ‘Costa’, the mountain ranges of the Andes, largest island is Isabela, which is 120 km long. Santo known as the ‘Sierra’, and the eastern lowlands or ‘Ori- Tomás, located on Isabela Island, is the highest peak of ente’, which form part of the Amazon River basin. -
JUDD W.S. Et. Al. (1999) Plant Systematics
CHAPTER8 Phylogenetic Relationships of Angiosperms he angiosperms (or flowering plants) are the dominant group of land Tplants. The monophyly of this group is strongly supported, as dis- cussed in the previous chapter, and these plants are possibly sister (among extant seed plants) to the gnetopsids (Chase et al. 1993; Crane 1985; Donoghue and Doyle 1989; Doyle 1996; Doyle et al. 1994). The angio- sperms have a long fossil record, going back to the upper Jurassic and increasing in abundance as one moves through the Cretaceous (Beck 1973; Sun et al. 1998). The group probably originated during the Jurassic, more than 140 million years ago. Cladistic analyses based on morphology, rRNA, rbcL, and atpB sequences do not support the traditional division of angiosperms into monocots (plants with a single cotyledon, radicle aborting early in growth with the root system adventitious, stems with scattered vascular bundles and usually lacking secondary growth, leaves with parallel venation, flow- ers 3-merous, and pollen grains usually monosulcate) and dicots (plants with two cotyledons, radicle not aborting and giving rise to mature root system, stems with vascular bundles in a ring and often showing sec- ondary growth, leaves with a network of veins forming a pinnate to palmate pattern, flowers 4- or 5-merous, and pollen grains predominantly tricolpate or modifications thereof) (Chase et al. 1993; Doyle 1996; Doyle et al. 1994; Donoghue and Doyle 1989). In all published cladistic analyses the “dicots” form a paraphyletic complex, and features such as two cotyle- dons, a persistent radicle, stems with vascular bundles in a ring, secondary growth, and leaves with net venation are plesiomorphic within angio- sperms; that is, these features evolved earlier in the phylogenetic history of tracheophytes. -
First Record of Taeniophyllum (Orchidaceae) in Myanmar
Gardens’ Bulletin Singapore 64(1): 133–137. 2012 133 First record of Taeniophyllum (Orchidaceae) in Myanmar H. Kurzweil1 and S. Lwin2 1 Herbarium, Singapore Botanic Gardens, 1 Cluny Road, Singapore 259569 [email protected] 2 Myanmar Floriculturist Association, Ahlone Road, Yangon, Myanmar ABSTRACT. Taeniophyllum Blume was recently discovered in northern Myanmar, a new generic record for the country. The Myanmar specimens are referred to the widespread species T. glandulosum Blume, characterised by terete roots, warty inflorescence axes, distichous bracts, sepals and petals basally fused into a tube about as long as their ovate-lanceolate free parts, and an ovate-lanceolate lip with a globose spur. Keywords. Myanmar, Taeniophyllum Introduction While undertaking fieldwork near Lake Inndawgyi in Kachin State, Myanmar, the authors of this article came across a leafless epiphytic orchid and recognised it as member of the genus Taeniophyllum Blume. Subsequent studies revealed that this genus has not yet been recorded in Myanmar (Govaerts et al. 2011, Kress et al. 2003, P. Ormerod pers. comm.). The genus Taeniophyllum comprises about 120 species, which are distributed from Sri Lanka and India throughout tropical and subtropical Asia eastwards as far as Japan, Australia and several Pacific islands, with a single species found in tropical Africa. Given the fact that Taeniophyllum occurs in all surrounding countries, its newly discovered occurrence in Myanmar is not surprising. Using recent orchid flora treatments (particularly Jayaweera 1981; Seidenfaden 1988, 1992; Seidenfaden & Wood 1992; Pearce & Cribb 2002; Chen & Wood 2009), the plants could be positively identified asT. glandulosum Blume. This species belongs to a taxonomically difficult complex of several closely related species, and several botanists have recently pointed out the need for further studies. -
Epilist 1.0: a Global Checklist of Vascular Epiphytes
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2021 EpiList 1.0: a global checklist of vascular epiphytes Zotz, Gerhard ; Weigelt, Patrick ; Kessler, Michael ; Kreft, Holger ; Taylor, Amanda Abstract: Epiphytes make up roughly 10% of all vascular plant species globally and play important functional roles, especially in tropical forests. However, to date, there is no comprehensive list of vas- cular epiphyte species. Here, we present EpiList 1.0, the first global list of vascular epiphytes based on standardized definitions and taxonomy. We include obligate epiphytes, facultative epiphytes, and hemiepiphytes, as the latter share the vulnerable epiphytic stage as juveniles. Based on 978 references, the checklist includes >31,000 species of 79 plant families. Species names were standardized against World Flora Online for seed plants and against the World Ferns database for lycophytes and ferns. In cases of species missing from these databases, we used other databases (mostly World Checklist of Selected Plant Families). For all species, author names and IDs for World Flora Online entries are provided to facilitate the alignment with other plant databases, and to avoid ambiguities. EpiList 1.0 will be a rich source for synthetic studies in ecology, biogeography, and evolutionary biology as it offers, for the first time, a species‐level overview over all currently known vascular epiphytes. At the same time, the list represents work in progress: species descriptions of epiphytic taxa are ongoing and published life form information in floristic inventories and trait and distribution databases is often incomplete and sometimes evenwrong. -
Do Orchids Grow in Hawaii? and How!
Do Orchids Grow in Hawaii? And How! SYNOPSIS This is an historical sketch of the Saga of Orchids in Hawaii. The sequence of events from the incidental introduction of species by the Agriculturists for the Sugar Industry; to their efforts in propagation and culture, hybridizing and germination; to the development of personal nurseries to commercial ranges; and ultimately to the creation of a viable orchid industry, re cognized world wide; to the natural formation of orchid societies staging of orchid shows; and finally to the introduction of a system of orchid judging , should bring interesting reading to orchidists, amateur and professional alike. In fact, this could serve as a reference syllabus to keep. DO ORCHIDS GROW IM HAWAII? AMD HOW i Compiled and Edited by Dr. T. David Woo and Wallace K. Nakamoto Published under the auspices of The Hawaii Orchid Foundation for the American Orchid Society, Inc. Hawaii Regional Judging Center 1990 i TABLE OF CONTE NTS TABLE OF CONTENTS.................................................................................... i PREFACE........................................................................................................ vii PART I. INTRODUCTION OF ORCHIDS TO HAWAII.............................................. 1 The History of Orchids in Hawaii by Dr. T. David Woo ................................................................... 3 Development of Floriculture in Hawaii by J. H. Beaumont ................................................ 10 A Short History of Orchids in Hawaii by Loraine -
The Island Rule and Its Application to Multiple Plant Traits
The island rule and its application to multiple plant traits Annemieke Lona Hedi Hendriks A thesis submitted to the Victoria University of Wellington in partial fulfilment of the requirements for the degree of Master of Science in Ecology and Biodiversity Victoria University of Wellington, New Zealand 2019 ii “The larger the island of knowledge, the longer the shoreline of wonder” Ralph W. Sockman. iii iv General Abstract Aim The Island Rule refers to a continuum of body size changes where large mainland species evolve to become smaller and small species evolve to become larger on islands. Previous work focuses almost solely on animals, with virtually no previous tests of its predictions on plants. I tested for (1) reduced floral size diversity on islands, a logical corollary of the island rule and (2) evidence of the Island Rule in plant stature, leaf size and petiole length. Location Small islands surrounding New Zealand; Antipodes, Auckland, Bounty, Campbell, Chatham, Kermadec, Lord Howe, Macquarie, Norfolk, Snares, Stewart and the Three Kings. Methods I compared the morphology of 65 island endemics and their closest ‘mainland’ relative. Species pairs were identified. Differences between archipelagos located at various latitudes were also assessed. Results Floral sizes were reduced on islands relative to the ‘mainland’, consistent with predictions of the Island Rule. Plant stature, leaf size and petiole length conformed to the Island Rule, with smaller plants increasing in size, and larger plants decreasing in size. Main conclusions Results indicate that the conceptual umbrella of the Island Rule can be expanded to plants, accelerating understanding of how plant traits evolve on isolated islands. -
Diversity and Roles of Mycorrhizal Fungi in the Bee Orchid Ophrys Apifera
Diversity and Roles of Mycorrhizal Fungi in the Bee Orchid Ophrys apifera By Wazeera Rashid Abdullah April 2018 A Thesis submitted to the University of Liverpool in fulfilment of the requirement for the degree of Doctor in Philosophy Table of Contents Page No. Acknowledgements ............................................................................................................. xiv Abbreviations ............................................................................ Error! Bookmark not defined. Abstract ................................................................................................................................... 2 1 Chapter one: Literature review: ........................................................................................ 3 1.1 Mycorrhiza: .................................................................................................................... 3 1.1.1Arbuscular mycorrhiza (AM) or Vesicular-arbuscular mycorrhiza (VAM): ........... 5 1.1.2 Ectomycorrhiza: ...................................................................................................... 5 1.1.3 Ectendomycorrhiza: ................................................................................................ 6 1.1.4 Ericoid mycorrhiza, Arbutoid mycorrhiza, and Monotropoid mycorrhiza: ............ 6 1.1.5 Orchid mycorrhiza: ................................................................................................. 7 1.1.5.1 Orchid mycorrhizal interaction: ...................................................................... -
E29695d2fc942b3642b5dc68ca
ISSN 1409-3871 VOL. 9, No. 1—2 AUGUST 2009 Orchids and orchidology in Central America: 500 years of history CARLOS OSSENBACH INTERNATIONAL JOURNAL ON ORCHIDOLOGY LANKESTERIANA INTERNATIONAL JOURNAL ON ORCHIDOLOGY Copyright © 2009 Lankester Botanical Garden, University of Costa Rica Effective publication date: August 30, 2009 Layout: Jardín Botánico Lankester. Cover: Chichiltic tepetlauxochitl (Laelia speciosa), from Francisco Hernández, Rerum Medicarum Novae Hispaniae Thesaurus, Rome, Jacobus Mascardus, 1628. Printer: Litografía Ediciones Sanabria S.A. Printed copies: 500 Printed in Costa Rica / Impreso en Costa Rica R Lankesteriana / International Journal on Orchidology No. 1 (2001)-- . -- San José, Costa Rica: Editorial Universidad de Costa Rica, 2001-- v. ISSN-1409-3871 1. Botánica - Publicaciones periódicas, 2. Publicaciones periódicas costarricenses LANKESTERIANA i TABLE OF CONTENTS Introduction 1 Geographical and historical scope of this study 1 Political history of Central America 3 Central America: biodiversity and phytogeography 7 Orchids in the prehispanic period 10 The area of influence of the Chibcha culture 10 The northern region of Central America before the Spanish conquest 11 Orchids in the cultures of Mayas and Aztecs 15 The history of Vanilla 16 From the Codex Badianus to Carl von Linné 26 The Codex Badianus 26 The expedition of Francisco Hernández to New Spain (1570-1577) 26 A new dark age 28 The “English American” — the journey through Mexico and Central America of Thomas Gage (1625-1637) 31 The renaissance of science -
Floristic Relationships of New Caledonian Rainforest Phanerogams
Extract from Telopea 2(6): 631-679 (1986) 63 1 FLORISTIC RELATIONSHIPS OF NEW CALEDONIAN RAINFOREST PHANEROGAMS PH.MORAT!, J.-M. VELLONI& H. S. MACKEE~ (Accepted for publication 16.9.1983) ABSTRACT Morat, Ph.’, Veìllon, J.-M.’ & MacKee, H. S.2 (‘Centre ORSTOM, B.P. A5 Cedex, Nouméa, New Caledonia; 2L3.P. 3349, Nouméa, New Caledonia) 1984. Floristic relatiomhips of New Caledonian rainforest phanerogams. Telopea 2[4): 631-679 - A detailed analysis of the New Caledonian rainforest flora is given; 1499 species in 365 genera and 108 families are listed. Distribution of the species within New Caledonia is given in terms of specificity to rainforest (forestInon-forest and forest occurrence) and to substrate (only ultrabasiclabsent from ultrabasic/present on ultrabasic and other substr: :ss). Distribution of genera is presented according’to occurrences in 12 phyto- geographic units from endemic to pantropical. Sources of information are given. Comparisons with the whole New Caledonian phanerogamic flora are made; 46% of genera and species and 66% of families occur in the rainforest. For the flora the level of specific endemism is c. 75%. Floristic affinities are assessed by: comparison of numbers of genera shared with other regions (pantropical genera included/excluded); and numbers of genera shared exclusively by New Caledonia and 2, 3, 4, 5 or 6 other regions. In these comparisons Australia, New Guinea, Malesia, Fiji, the New Hebrides, the Solomon Islands and then New Zealand have the most genera in common with New Caledonia. A floristic affinity Co-efficient for each territory was calculated from the proportion of the number of common genera to the number of territories in which they occur, for groups of two to six territories. -
Chromosome Numbers and Polyploidy Events in Korean Non-Commelinids Monocots: a Contribution to Plant Systematics
pISSN 1225-8318 − Korean J. Pl. Taxon. 48(4): 260 277 (2018) eISSN 2466-1546 https://doi.org/10.11110/kjpt.2018.48.4.260 Korean Journal of REVIEW Plant Taxonomy Chromosome numbers and polyploidy events in Korean non-commelinids monocots: A contribution to plant systematics Tae-Soo JANG* and Hanna WEISS-SCHNEEWEISS1 Department of Biological Science, College of Bioscience and Biotechnology, Chungnam National University, Daejeon 34134, Korea 1Department of Botany and Biodiversity Research, University of Vienna, A-1030 Vienna, Austria (Received 4 June 2018; Revised 9 September 2018; Accepted 16 December 2018) ABSTRACT: The evolution of chromosome numbers and the karyotype structure is a prominent feature of plant genomes contributing to or at least accompanying plant diversification and eventually leading to speciation. Polyploidy, the multiplication of whole chromosome sets, is widespread and ploidy-level variation is frequent at all taxonomic levels, including species and populations, in angiosperms. Analyses of chromosome numbers and ploidy levels of 252 taxa of Korean non-commelinid monocots indicated that diploids (ca. 44%) and tet- raploids (ca. 14%) prevail, with fewer triploids (ca. 6%), pentaploids (ca. 2%), and hexaploids (ca. 4%) being found. The range of genome sizes of the analyzed taxa (0.3–44.5 pg/1C) falls well within that reported in the Plant DNA C-values database (0.061–152.33 pg/1C). Analyses of karyotype features in angiosperm often involve, in addition to chromosome numbers and genome sizes, mapping of selected repetitive DNAs in chro- mosomes. All of these data when interpreted in a phylogenetic context allow for the addressing of evolution- ary questions concerning the large-scale evolution of the genomes as well as the evolution of individual repeat types, especially ribosomal DNAs (5S and 35S rDNAs), and other tandem and dispersed repeats that can be identified in any plant genome at a relatively low cost using next-generation sequencing technologies. -
Species Diversity of Orchids in Bukit Barisan Selatan National Park, Lampung, Indonesia
BIODIVERSITAS ISSN: 1412-033X Volume 20, Number 1, January 2019 E-ISSN: 2085-4722 Pages: 343-349 DOI: 10.13057/biodiv/d200140 Species diversity of Orchids in Bukit Barisan Selatan National Park, Lampung, Indonesia ESTI MUNAWAROH♥, YUZAMMI♥♥ Center for Plant Conservation Botanic Gardens, Indonesia Institut of Sciences. Jl. Ir. H. Juanda 13, Bogor 16122, West Java, Indonesia Tel./fax. +62-251-8322187 ♥email: [email protected] ♥♥ [email protected] Manuscript received: 28 September 2018. Revision accepted: 30 December 2018. Abstract. Munawaroh E, Yuzammi. 2019. Species diversity of Orchids in Bukit Barisan Selatan National Park, Lampung, Indonesia. Biodiversitas 20: xxxx. Orchids, belonging to the family Orchidaceae, are well known ornamental plants due to their beautiful flowers and varied colors. The members of this family have received more scientific attention than other plant families because of their unique botanical features and economic value. This study was conducted to explore and record the species diversity of Orchidaceae in Sumatera, especially in the Bukit Barisan Selatan National Park (BBSNP), Lampung, Indonesia. This research was carried out from 2011 to 2014 at four locations, namely Kubu Perahu Resort, Sukaraja Atas Resort, Pugung Tampak Resort and Sekincau Resort, using purposive sampling method. A total of 132 species belonging to 52 genera of orchids have been identified from BBSNP, Lampung, of which 37 genera are epiphytic orchids and 15 genera are terrestrial orchids. Two species namely, Vanda sumatrana and Grammatophyllum speciosum, have been recognized as protected species. Vanda sumatrana is also endemic to Sumatera. These orchids are also cultivated at Liwa Botanic Garden, as an ex situ conservation. -
MID-AMERICA ORCHID CLASSIFICATION July 1, 2014 Name Abbreviation Class Species Hybrid a Abaxianthus (See Flickingeria) Abdominea (See Robiquetia) Aberconwayara Acw
MID-AMERICA ORCHID CLASSIFICATION July 1, 2014 Name Abbreviation Class Species Hybrid A Abaxianthus (see Flickingeria) Abdominea (see Robiquetia) Aberconwayara Acw. 13 Aberrantia (see Pleurothallis) Abola (see Caucaea) Acacallis (see Aganisia) Acampe Acp. 68 69 Acampodorum (see Aracampe) Acampostylis Acy. 65 Acanthephippium Aca. 98 99 Acapetalum Acpt. 95 Aceras (see Orchis) Acerasherminium (see Hermorchis) Acianthera Acia. 92 Acianthus Aci. 98 99 Acinbreea Acba. 99 Acineta Acn. 98 99 Acinopetala (see Masdevallia) Aciopea Aip. 99 Acoridium (see Dendrochilum) Acostaea Asa. 92 Acriopsis Acr. 98 99 Acrolophia Apa. 81 Acronia (see Pleurothallis) Acropera (see Gongora) Acrorchis Arr. 98 99 Ada (see Brassia) Adachilum (see Brassochilum) Adacidiglossum Adg. 76 Adacidium (see Brassidium) Adaglossum (see Odontobrassia) Adamara Adm. 17-25 Adapasia (see Brapasia) Adelopetalum (see Bulbophyllum) Adenoncos Ade. 68 69 Adioda (see Brassioda) Adonclioda (see Maccullyara) Adoncostele (see Brascidostele) Aerachnochilus (see Paulsenara) Aerangaeris Arg. 58 Aeranganthes Argt. 58 Aerangis Aergs. 58 Aeranthes Aerth. 68 69 Aerasconetia (see Aeridovanda) Aeridachnanthe Aed. 66 Aeridachnis Aerdns. 66 Aeridanthe (see Aeridovanda) Aerides Aer. 66 Aeridisia (see Luisaerides) Aeriditis (see Aeridopsis) Aeridocentrum (see Aeridovanda) Aeridochilus Aerchs. 66 Aeridofinetia (see Aeridovanda) Aeridoglossum (see Renades) Page 2 Mid-America Orchid Classification, July 1, 2014 Name Abbreviation Class Species Hybrid Aeridoglottis Aegts. 66 Aeridopsis Aerps. 66 Aeridopsisanthe (see Maccoyara) Aeridostachya (see Eria) Aeridovanda Aerdv. 69 Aeridovanisia Aervsa. 66 Aeridsonia (see Aeridovanda) Aeristomanda Atom. 66 Aeroeonia Aoe. 58 Agananthes Agths. 95 Aganax (see Pabanisia) Aganella All. 78 Aganisia Agn. 95 Aganopeste Agt. 93 Agasepalum Agsp. 95 Agrostophyllum Agr. 98 99 Aitkenara Aitk. 95 Alamania Al. 16 25 Alangreatwoodara (see Propabstopetalum) Alantuckerara Atc. 95 Alaticaulia (see Masdevallia) Alatiglossum (see Gomesa) Alcockara (see Ledienara) Alexanderara (see Maclellanara) Aliceara Alcra.