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Phylogenetic Placement of the Enigmatic Orchid Genera Thaia and Tangtsinia: Evidence from Molecular and Morphological Characters
TAXON 61 (1) • February 2012: 45–54 Xiang & al. • Phylogenetic placement of Thaia and Tangtsinia Phylogenetic placement of the enigmatic orchid genera Thaia and Tangtsinia: Evidence from molecular and morphological characters Xiao-Guo Xiang,1 De-Zhu Li,2 Wei-Tao Jin,1 Hai-Lang Zhou,1 Jian-Wu Li3 & Xiao-Hua Jin1 1 Herbarium & State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, P.R. China 2 Key Laboratory of Biodiversity and Biogeography, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan 650204, P.R. China 3 Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Menglun Township, Mengla County, Yunnan province 666303, P.R. China Author for correspondence: Xiao-Hua Jin, [email protected] Abstract The phylogenetic position of two enigmatic Asian orchid genera, Thaia and Tangtsinia, were inferred from molecular data and morphological evidence. An analysis of combined plastid data (rbcL + matK + psaB) using Bayesian and parsimony methods revealed that Thaia is a sister group to the higher epidendroids, and tribe Neottieae is polyphyletic unless Thaia is removed. Morphological evidence, such as plicate leaves and corms, the structure of the gynostemium and the micromorphol- ogy of pollinia, also indicates that Thaia should be excluded from Neottieae. Thaieae, a new tribe, is therefore tentatively established. Using Bayesian and parsimony methods, analyses of combined plastid and nuclear datasets (rbcL, matK, psaB, trnL-F, ITS, Xdh) confirmed that the monotypic genus Tangtsinia was nested within and is synonymous with the genus Cepha- lanthera, in which an apical stigma has evolved independently at least twice. -
Aerangis Articulata by Brenda Oviatt and Bill Nerison an Exquisite Star from Madagascar
COLLECTor’s item by Brenda Oviatt and Bill Nerison Aerangis articulata An Exquisite Star from Madagascar IN ALL HONESTY, WHEN WE FOUND out that our photo of Aerangis articulata was chosen for the cover of Isobyl la Croix’s (2014) new book Aerangis, we were more than just a little excited! We decided that this is a perfect opportunity to tell people more about Aergs. articulata and give an introduction to her new book. We will try and help clarify the confusion surrounding the identification of this species, describe what to look for if you intend to buy one and discuss culture to help you grow and bloom it well. We love angraecoids, and the feature that most share and what sets them apart is their spurs or nectaries. In some orchid species, attracting the pollinator is all about fooling someone (quite often an insect). Some will mimic a female insect while others will mimic another type of flower to attract that flower’s pollinator. Oftentimes the u n s u s p e c t i n g insect gets nothing in return; not the promised mate or the nectar of the Brenda Oviatt and mimicked flower. Bill Nerison With angraecoids, the pollinator is often rewarded with a sweet treat: nectar that sits in the bottom of the spur. The pollinator of Aergs. articulata is a hawk moth (DuPuy, et al 1999) whose proboscis can reach that nectar. These moths are attracted by the sweet nighttime fragrance TT (scented much like a gardenia) and by the A VI O white flower (more visible than a colored A D flower in the dark). -
Atlanta Orchid Society Newsletter
The Atlanta Affiliated with the American Orchid Orchid Society, the Orchid Digest Corporation and the Mid-America Orchid Congress. Society 2001 Recipient of the American Orchid Society’s Distinguished Affiliated Bulletin Societies Service Award Newsletter Editor: Danny Lentz Volume 47: Number 7 www.atlantaorchidsociety.org July 2006 JULY EVENTS The Meeting: 8:00 Monday, July 10 at Atlanta Botanical Garden Marv Ragan will speak on Encyclias Marv Ragan of MAJ Orchids in Jacksonville will give a presentation on Encyclias. He will be bringing plants to sell. Roy Harrow’s Auction Roy Harrow’s auction will be held on July 29. This is a great opportunity to sell or swap some of your extra plants. See page 4 for details. Neomoorea irrorata Inside This Issue Atlanta Orchid Society 2006 Officers…………………………………………..….…………… Page 2 Member Spotlight – Mikie Emerson………………………………………...……....………….. Page 2 Events Out and About………………Dates for your Calendar…………...……….…….……… Page 3 Minutes of the June Meeting ….…….…...……….………….…………..……………...….…. Page 3 Roy Harrow’s Auction……………………….………..………..……………………………... Page 4 The June Exhibition Table ……………………………….………..………..…………...……. Page 5 Recent Blooms at the Atlanta Botanical Garden……………………………………………….. Page 8 Collector’s Item : Aeranthes ramosa Rolfe……………….………….…………..………...…… Page 9 Recent Awards from the Atlanta Judging Center……….………………………………………. Page 10 All contents © Atlanta Orchid Society unless otherwise noted. Page 2 www.atlantaorchidsociety.org July 2006 THE ATLANTA ORCHID Member Spotlight I am pretty much "plain vanilla." I SOCIETY have been growing orchids since Officers 1995. After killing quite a few, I President - Richard Hallberg decided I needed help so I joined both 152 Sloan St. AtlOS and South Metro Orchid Roswell, GA 30075 Society and the AOS. I grew in a back 770-587-5827 bedroom for a while then I built a [email protected] small attached greenhouse mainly built Vice-President/Programs - Mark Reinke from recycled material. -
The Angraecoid Alliance
Spring 2013 THE ANGRAECOID ALLIANCE Angraecum stella-africae by Isobyl la Croix Volume 2: The 21st World Orchid Conference plants of Bulbophyllum josephii. will be held in Johannesburg in There were several mature plants and Issue 2 September 2014. The logo depicts some young ones on the trunk, one in Spring 2013 Angraecum stella-africae, so it seems flower and others in bud. Each an appropriate time to write about this mature plant bore a single large, little species. green, winged capsule, apparently I first became aware of this species from the previous year, and an old Inside this issue: when I was given a copy of Southern brown one that had shed its seed, African Epiphytic Orchids by John presumably from the year before that. Angraecum 1 Ball, where it is listed as Angraecum One or two other trees had a few stella-africae sp. (Renny 174). Like the other plants of the Angraecum and species covered in the book it is obviously none of the local people Ex-Situ illustrated by a life-size watercolour had been there recently to collect Conservation 3 painting by Patricia van de Ruit. It firewood, as we found one or two Update was known from what was then fallen branches carrying plants, which Transvaal (now Limpopo) in South we took home with us. Missouri Botanical Gardens: 25 years 4 Africa and there was an unconfirmed About 10 days later, Phillip Cribb, in Madagascar record from Zimbabwe. I thought the Kew orchid specialist, was on his what an attractive plant it was, but it way back from a conference in South never occurred to me that we might Africa and stayed with us for a couple World Orchid later find it ourselves. -
Ants Tend Ghost Orchids: Patrolling of Dendrophylax Lindenii (Orchidaceae) by Crematogaster Ashmeadi in Florida
Ants tend ghost orchids: patrolling of Dendrophylax lindenii (Orchidaceae) by Crematogaster ashmeadi in Florida Peter R. Houlihan1,5,*, Andrea Lucky2, Mike Owen3, and Thomas C. Emmel1,2,4,6 Abstract Myriad symbioses exist between insects and orchids, especially in tropical forests where the majority of species are epiphytic. Relationships be- tween ants and rare epiphytic orchids are underrepresented in the scientific literature. The natural history and ecological entomology of Florida’s endangered and epiphytic ghost orchid, Dendrophylax lindenii (Lindley) Bentham ex Rolfe (Orchidaceae), remain limited. Widely recognized for long-standing hypotheses concerning the species’ pollination ecology, that documentation recently overturned, other interactions between insects and ghost orchids are scarce. Here we describe the first associations between ants, Crematogaster ashmeadi Mayr (Hymenoptera: For- micidae), and D. lindenii. Ghost orchid roots provide facultative and opportunistic structures for arboreal ants to use in nesting. Furthermore, excrement from ant colonies within the root mass can increase nutrient availability in the orchid’s nutrient-poor substrate; the proximity of these ants permits patrolling to defend the plant and exert control over possible extra floral nectaries that require further inquiry. This study presents novel observations that expand the known insect associations with ghost orchids, elucidating the complex ecology of one of Florida’s rarest and most endangered species. Key Words: ants; arboreal; ecology; epiphyte; Everglades; Fakahatchee Resumen Existen incontables números de simbiosis entre insectos y orquídeas, especialmente en los bosques tropicales donde la mayoría de las especies son epífitas. Las relaciones entre las hormigas y las orquídeas epífitas más raras están subrepresentadas en la literatura científica. -
Lankesteriana No. 5
LANKESTERIANA 5: 27-30. 2002. A NEW SPECIES OF STELLILABIUM SECTION TAENIORHACHIS (ORCHIDACEAE) FROM COSTA RICA 1 2 FRANCO PUPULIN and MARIO A. BLANCO 1 Jardín Botánico Lankester, Universidad de Costa Rica P.O. Box 1031-7050 Cartago, Costa Rica, A.C. - [email protected] Research Associate, Marie Selby Botanical Gardens, Sarasota, USA 2 Instituto Centroamericano de Investigación Biológica y Conservación P.O. Box 2398-250, San Pedro de Montes de Oca, San José, Costa Rica Research Associate, Jardín Botánico Lankester, Universidad de Costa Rica Present mailing address: University of Florida, Department of Botany, 220 Bartram Hall P.O. Box 118526 Gainesville, Florida 32611-8526, U.S.A. [email protected] RE S U M E N. Se describe e ilustra Stellilabium smaragdinum de los bosques montanos de encino de la Cordillera de Talamanca. S. smaragdinum se distingue de otras especies de la sección Taeniorhachis por su inflorescencia con 1 a 3 (4) flores simultáneas, los lóbulos basales del labelo oblongos a ovoides y redondeados en el ápice y la peculiar coloración de la setas en los lóbulos laterales de la columna, marfil con bandas púrpura. ABSTRACT. The new species Stellilabium smaragdinum is described and illustrated from the montane oak forests of the Cordillera de Talamanca, Costa Rica. Among the species of Sect. T a e n i o r h a c h i s, S . smaragdinum may be recognized for the inflorescence bearing 1-3 (4) simultaneous flowers, the oblong to ovoid, rounded basal lobules of the lip, the non-ciliate margins of the lip midlobe and the peculiar colour of the column setae, cream banded with purple. -
Orchid Historical Biogeography, Diversification, Antarctica and The
Journal of Biogeography (J. Biogeogr.) (2016) ORIGINAL Orchid historical biogeography, ARTICLE diversification, Antarctica and the paradox of orchid dispersal Thomas J. Givnish1*, Daniel Spalink1, Mercedes Ames1, Stephanie P. Lyon1, Steven J. Hunter1, Alejandro Zuluaga1,2, Alfonso Doucette1, Giovanny Giraldo Caro1, James McDaniel1, Mark A. Clements3, Mary T. K. Arroyo4, Lorena Endara5, Ricardo Kriebel1, Norris H. Williams5 and Kenneth M. Cameron1 1Department of Botany, University of ABSTRACT Wisconsin-Madison, Madison, WI 53706, Aim Orchidaceae is the most species-rich angiosperm family and has one of USA, 2Departamento de Biologıa, the broadest distributions. Until now, the lack of a well-resolved phylogeny has Universidad del Valle, Cali, Colombia, 3Centre for Australian National Biodiversity prevented analyses of orchid historical biogeography. In this study, we use such Research, Canberra, ACT 2601, Australia, a phylogeny to estimate the geographical spread of orchids, evaluate the impor- 4Institute of Ecology and Biodiversity, tance of different regions in their diversification and assess the role of long-dis- Facultad de Ciencias, Universidad de Chile, tance dispersal (LDD) in generating orchid diversity. 5 Santiago, Chile, Department of Biology, Location Global. University of Florida, Gainesville, FL 32611, USA Methods Analyses use a phylogeny including species representing all five orchid subfamilies and almost all tribes and subtribes, calibrated against 17 angiosperm fossils. We estimated historical biogeography and assessed the -
A Review of CITES Appendices I and II Plant Species from Lao PDR
A Review of CITES Appendices I and II Plant Species From Lao PDR A report for IUCN Lao PDR by Philip Thomas, Mark Newman Bouakhaykhone Svengsuksa & Sounthone Ketphanh June 2006 A Review of CITES Appendices I and II Plant Species From Lao PDR A report for IUCN Lao PDR by Philip Thomas1 Dr Mark Newman1 Dr Bouakhaykhone Svengsuksa2 Mr Sounthone Ketphanh3 1 Royal Botanic Garden Edinburgh 2 National University of Lao PDR 3 Forest Research Center, National Agriculture and Forestry Research Institute, Lao PDR Supported by Darwin Initiative for the Survival of the Species Project 163-13-007 Cover illustration: Orchids and Cycads for sale near Gnommalat, Khammouane Province, Lao PDR, May 2006 (photo courtesy of Darwin Initiative) CONTENTS Contents Acronyms and Abbreviations used in this report Acknowledgements Summary _________________________________________________________________________ 1 Convention on International Trade in Endangered Species (CITES) - background ____________________________________________________________________ 1 Lao PDR and CITES ____________________________________________________________ 1 Review of Plant Species Listed Under CITES Appendix I and II ____________ 1 Results of the Review_______________________________________________________ 1 Comments _____________________________________________________________________ 3 1. CITES Listed Plants in Lao PDR ______________________________________________ 5 1.1 An Introduction to CITES and Appendices I, II and III_________________ 5 1.2 Current State of Knowledge of the -
The Orchid Flora of the Colombian Department of Valle Del Cauca Revista Mexicana De Biodiversidad, Vol
Revista Mexicana de Biodiversidad ISSN: 1870-3453 [email protected] Universidad Nacional Autónoma de México México Kolanowska, Marta The orchid flora of the Colombian Department of Valle del Cauca Revista Mexicana de Biodiversidad, vol. 85, núm. 2, 2014, pp. 445-462 Universidad Nacional Autónoma de México Distrito Federal, México Available in: http://www.redalyc.org/articulo.oa?id=42531364003 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Revista Mexicana de Biodiversidad 85: 445-462, 2014 Revista Mexicana de Biodiversidad 85: 445-462, 2014 DOI: 10.7550/rmb.32511 DOI: 10.7550/rmb.32511445 The orchid flora of the Colombian Department of Valle del Cauca La orquideoflora del departamento colombiano de Valle del Cauca Marta Kolanowska Department of Plant Taxonomy and Nature Conservation, University of Gdańsk. Wita Stwosza 59, 80-308 Gdańsk, Poland. [email protected] Abstract. The floristic, geographical and ecological analysis of the orchid flora of the department of Valle del Cauca are presented. The study area is located in the southwestern Colombia and it covers about 22 140 km2 of land across 4 physiographic units. All analysis are based on the fieldwork and on the revision of the herbarium material. A list of 572 orchid species occurring in the department of Valle del Cauca is presented. Two species, Arundina graminifolia and Vanilla planifolia, are non-native elements of the studied orchid flora. The greatest species diversity is observed in the montane regions of the study area, especially in wet montane forest. -
How to Grow the Ghost Orchid
How to Grow the Ghost Orchid: DENDROPHYLAX lindenii is a rare plant in the wild as well as in collections. Hopefully, increased interest and uncovering some of its cultural secrets will lead to more of these jewels of nature being grown. The number one requirement for maintaining a healthy ghost orchid is finding a suitable substrate. Whatever is used must not decay for decades, must have some sort of patina such as moss and lichens, hold some moisture for a length of time after watering, and have a rough and variable texture. In the wild, these plants grow on live trees, and as long as the tree is alive, the bark that the plant is attached to maintains its integrity. Dendrophylax lindenii can be long lived and will take several years to develop into a blooming-size plant. For this reason, the substrate must also be long lasting or the grower will not see the 1 2 beloved plant live long enough to bloom consistently. In the wild, the tree’s bark restaurants that use real hickory for [1] A four-year-old seedling of Dlax. lindenii is covered with a mix of various lichens, cooking, mills that manufacture tool from flask mounted to a new hickory mosses and other hosts that add to the handles and salvaged trees from storm bark slab. Old roots showing new orchid’s microenvironment by providing damage. The bark is nearly impossible to growing tips and several new roots remove from fresh-cut trees. I leave the moisture directly to the roots, as well as emerging from crown can be seen. -
A Ghostly Pursuit Developing a Passion for the Ghost Orchid by KEITH DAVIS
A Ghostly Pursuit Developing a Passion for the Ghost Orchid BY KEITH DAVIS IN AUTUMN 1980, THIS MISPLACED winning touchdown of the Super Bowl, bachelor cruised down one street after then carried my 10-pound (4.5-kg) prize another, looking for yard sales in the to Red. uppercrust neighborhoods of Corpus Locking the book in the car, I Christi. Sitting barely 6 inches (15 cm) decided to go back to look at the off the pavement in my 1968 Triumph strange plants that filled such a huge GT-6 named “Red,” I saw hordes of portion of the lawn. Some plants had people converging on the front lawn tall canes, sort of bamboolike, some of a stately southern Texas home. This had large fan-shaped leaves not unlike particular sale had folding tables a palm seedling, some had flat leaves packed with every imaginable dust like two ranks of beaver tails, and others collector known to man as well as rack had fat clublike stems with one or two after rack stocked with once-stylish large stiff leaves on top. Many were in clothes. The 100-plus people crowding large 8- to 12-inch (20- to 30-cm) clay the yard were gathering around a large pots, while others were in baskets made section that had loosely organized of wood. Strangest of all were the ones rows of books and magazines. The left mounted on cork bark and something side of the yard was completely that looked to me like little bits of black covered with hundreds of odd-looking sticks glued together. -
Cytotaxonomy of the Monopodial Orchids of the African and Malagasy Regions
Cytotaxonomy of the monopodial orchids of the African and Malagasy regions J. C. Arends & F. M. Van der Laan Department of Plant Taxonomy and Plant Geography, Agricultural University, Gen. Foulkesweg 37, 6700 ED Wageningen, The Netherlands Abstract The three subtribes which are recognized within the tribe Vandeae are represented in the tropical African and Malagasy regions. All taxa of the Vandeae have a monopodial growth habit. The first subtribe, Sarcanthinae, is mainly Asian-Australasian, but a few of its species occur in Madagascar and in Africa. The other two subtribes, Angraecinae and Aerangidinae, are both represented in the latter two regions. The Angraecinae ischaracterize d by the presence of a short rostellum, but this iselongate d in the Aerangidinae. According to earlier authors there is a correlation between presence of the short rostellum and a basic chromosome number of x= 19i nth e Angraecinae, and between the presence of an elongated rostellum and a basic number of x = 25 in the Aerangidinae. The results presented in this paper are placed in perspective with the chromosome numbers recorded by other authors. From the resulting chromosome number survey it appears that only part of the Angraecinae (Aeranthes, several species of Angraecum. Cryptopus and Jumellea) have a basic number of x = 19; some members of the Angraecinae (other species of Angraecum) were found to have a basic number of x = 21,24 and 25. The Aerangidinae is not characterized by a single basic number of x= 25 but by aserie s ranging from x = 23t o x= 27,o f which x= 23,24 and 25ar e the most frequent.