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New Cattleya Orchid Hybrid(1)
GUILHERME AUGUSTO CITO ALVES CORREIO et. al 145 CULTIVAR DESCRIPTION New Cattleya orchid hybrid(1) GUILHERME AUGUSTO CITO ALVES(2), RODRIGO THIBES HOSHINO(2), DOUGLAS JUNIOR BERTONCELLI(2), RONAN CARLOS COLOMBO(2), VANESSA STEGANI(3), RICARDO TADEU DE FARIA(2) ABSTRACT The hybrid, obtained by back crossing between (Cattleya labiata x Cattleya forbesii) x Cattleya labiata is a vigorous plant, bi- or unifoliate, features slender and cylindrical pseudobulbs and leathery dark-greenish leaves, with oblanceolate shape format of blunt tips with the first flowering four years after sowing. In Londrina, flowering occurred twice a year, between the months of April and May and October and November with 2-4 flowers per pseudobulb and durability ranging from 15 to 20 days. The flowers of the new hybrid were purple with a labellum with a yellow center and purple stripes. Keywords: breeding, floriculture, Orchidaceae, selection. RESUMO Novo híbrido de orquídea Cattleya O híbrido, obtido do retrocruzamento entre (Cattleya labiata x Cattleya forbesii) x Cattleya labiata é uma planta vigorosa, bi ou unifoliada, apresenta pseudobulbos delgados e cilíndricos e folhas coriáceas com tonalidade verde escuro, com formato oblanceolado, de pontas obtusas, apresentando o primeiro florescimento após quatros anos da semeadura. O florescimento em Londrina ocorreu duas vezes no ano, entre os meses de abril e maio e outubro e novembro com 2-4 flores por pseudobulbo e durabilidade entre 15 a 20 dias. As flores do novo híbrido possuem coloração lilás e labelo com um centro amarelo e listras roxas. Palavras-chave: floricultura, melhoramento, Orchidaceae, seleção. 1. INTRODUCTION allows the introduction of relevant genes such as shape, durability, color, and others into hybrids of orchids The Orchidaceae family has about 26,500 species, (WITHNER, 1988) distributed across all continents (KEW, 2011). -
The Diversity of Wild Orchids in the Southern Slope of Mount Merapi, Yogyakarta, Indonesia Eight Years After the 2010 Eruption
BIODIVERSITAS ISSN: 1412-033X Volume 21, Number 9, September 2020 E-ISSN: 2085-4722 Pages: 4457-4465 DOI: 10.13057/biodiv/d210964 The diversity of wild orchids in the southern slope of Mount Merapi, Yogyakarta, Indonesia eight years after the 2010 eruption FEBRI YUDA KURNIAWAN1,2,♥, FAUZANA PUTRI2,3, AHMAD SUYOKO2,3, HIMAWAN MASYHURI2,3, MAYA PURQI SULISTIANINGRUM2,3, ENDANG SEMIARTI3,♥♥ 1Postgraduate School, Universitas Gadjah Mada. Jl. Teknika Utara, Sleman 55281, Yogyakarta, Indonesia. Tel./fax. +62-274-544975, email: [email protected] 2Biology Orchid Study Club (BiOSC), Faculty of Biology, Universitas Gadjah Mada. Jl. Teknika Selatan, Sekip Utara, Sleman 55281, Yogyakarta, Indonesia 3Department of Tropical Biology, Faculty of Biology, Universitas Gadjah Mada. Jl. Teknika Selatan, Sekip Utara, Sleman 55281, Yogyakarta, Indonesia. Tel./fax.: +62-274-580839, email: [email protected] Manuscript received: 21 August 2020. Revision accepted: 31 August 2020. Abstract. Kurniawan FY, Putri F, Suyoko A, Masyhuri H, Sulistianingrum MP, Semiarti E. 2020. The diversity of wild orchids in the southern slope of Mount Merapi, Yogyakarta, Indonesia eight years after the 2010 eruption. Biodiversitas 21: 4457-4465. The ecosystem of the slopes of Mount Merapi is mountain tropical forest which is frequently affected by volcanic activities. The dynamics of the volcano affect the diversity and abundance of orchids in the ecosystem. Tritis is an area included in the Turgo Hill of the southern slope of Mount Merapi and is under the management of Mount Merapi National Park. The ecosystem in Tritis area classified as lower mountain forest and it has been affected by Mount Merapi eruption. This study aimed to do an inventory of orchid species in Tritis to know the diversity and abundance of orchids that exist in this area. -
Platanthera Chapmanii: Culture, Population Augmentation, and Mycorrhizal Associations
Platanthera chapmanii: culture, population augmentation, and mycorrhizal associations By Kirsten Poff, B.S. A Thesis In Plant and Soil Science Submitted to the Graduate Faculty of Texas Tech University in Partial Fulfillment of the Requirements for the Degree of MASTER OF SCIENCE Approved Dr. Jyotsna Sharma Chair of Committee Dr. Scott Longing Dr. John Zak Dr. Mark Sheridan Dean of the Graduate School August, 2016 © 2016, Kirsten Poff Texas Tech University, Kirsten Poff, August 2016 ACKNOWLEDGEMENTS First I would like to thank my mentor and advisor, Dr. Jyotsna Sharma for all of her help and support. She has challenged and encouraged me throughout my program and the duration of this project. Thanks to her, I am light-years ahead of where I was two years ago. Texas Parks and Wildlife is also gratefully acknowledged for funding portions of this study. I also wish to express my gratitude to Dr. John Zak for his enthusiasm and for encouraging my love of microbes. I also gratefully thank Dr. Scott Longing for his advice, and constructive comments. I sincerely thank all three committee members for all the time and energy they have spent on me throughout the duration of my project. I gratefully acknowledge Dr. Jason Woodward for his encouragement and recommendations as well. I also acknowledge Dr. Cynthia McKenney and Mr. Russel Plowman for their support; I now have a passion for teaching, and a much better understanding of what it is like to teach college level courses. I want to also thank Mr. Robby Carlson for his time and technological assistance. -
ORCHID POLLINATION ECOLOGY Orchid Pollination Exploring a Fascinating World by Ron Mchatton
ORCHID POLLINATION ECOLOGY Orchid Pollination Exploring a Fascinating World BY RON MCHATTON [1] The first example of sexual deception in Australian orchids involved the genus Cryptostylis. These orchids are pollinated by male parasitic wasps of the genus Lissopimpla. Here four male Lissopimpla excelsa wasps compete for the favors of a Cryptostylis erecta flower. MARK CLEMENTS [2] Silver-spotted skipper (Epargyreus clarus) pollinating a small purple fringed orchid (Platanthera psycodes) at Mt. Mitchell, North Carolina. The long spurs of the orchid have nectar at their ends and the skipper must push its proboscis deep into the spur to get to the nectar. Note the pollinia attached to the base of JAMES PETRANKA JAMES the skipper’s proboscis. bumblebee species. In this case, pollinia of Den. infundibulum are placed on the head of the bee while that from the Cymbidium, with much longer column, becomes at- tached to the bee’s central thorax. Because the column of the former species is much shorter, only pollinia placed near the front of the bee will be in a position to contact the stigmatic surface of the Dendrobium column as the bee exits the flower (Du Puy and Cribb 2007). Orchids with large gullet flowers such as Cymbidium are typically pollinated by large carpenter bees and bumblebees are known to pollinate Spiranthes and are implicated in the pollination of northern NT NT U U and some high-elevation species where other large bees are less common or active. 3 4 ERIC H ERIC H Some bees gather oils from flowers rather than nectar or pollen and many orchids [3–4] Sobralia [3] and Cattleya [4], two gen- NO ONE IS REALLY SURE HOW LONG have evolved to attract these pollinators. -
Tese 2014 Cristiane Gouvêa Fajardo
UNIVERSIDADE FEDERAL DO RIO GRANDE DO NORTE CENTRO DE BIOCIÊNCIAS PROGRAMA DE PÓS- GRADUAÇÃO EM ECOLOGIA Conservação genética de Cattleya granulosa Lindley: uma orquídea ameaçada de extinção Tese de Doutorado Cristiane Gouvêa Fajardo Orientador: Dr. Wagner Franco Molina Co-orientador: Dr. Fábio de Almeida Vieira Natal-RN 2014 1 CRISTIANE GOUVÊA FAJARDO Conservação genética da orquídea Cattleya granulosa Lindley Tese de Doutorado apresentada como requisito para a obtenção do título de Doutor, pelo Programa de Pós-Graduação em Ecologia, Área de Ecologia Terrestre, Universidade Federal do Rio Grande do Norte. Natal-RN 2014 1 “O mundo é um lugar perigoso de se viver, não por causa daqueles que fazem o mal, mas sim por causa daqueles que observam e deixam o mal acontecer.” Albert Einstein 2 SUMÁRIO Apresentação ..................................................................................................................... 1 Resumo .............................................................................................................................. 2 Abstract .............................................................................................................................. 3 Introdução .......................................................................................................................... 4 Objetivos ............................................................................................................................ 8 Referências ....................................................................................................................... -
Aspectos Fisiológicos E Bioquímicos Da Morfogênese in Vitro De Dendrobium Phalaenopsis E Cattleya Labiata
UNIVERSIDADE FEDERAL RURAL DE PERNAMBUCO PROGRAMA DE PÓS-GRADUAÇÃO EM BOTÂNICA MAIZA DE AZEVEDO DANTAS Aspectos fisiológicos e bioquímicos da morfogênese in vitro de Dendrobium phalaenopsis e Cattleya labiata RECIFE-PE 2014 Maiza de Azevedo Dantas Aspectos fisiológicos e bioquímicos da morfogênese in vitro de Dendrobium phalaenopsis e Cattleya labiata Dissertação apresentada ao Programa de Pós-Graduação em Botânica da Universidade Federal Rural de Pernambuco como parte dos requisitos para obtenção do título de mestre em Botânica ORIENTADORA: Dra. Terezinha Rangel Câmara CO-ORIENTADORAS: Dra. Claudia Ulisses de Carvalho Silva Dra. Cintia Cavalcanti de Albuquerque RECIFE-PE 2014 iii Ficha catalográfica D192a Dantas, Maiza de Azevedo Aspectos fisiológicos e bioquímicos da morfogênese in vitro de Dendrobium phalaenopsis e Cattleya labiata / Maiza de Azevedo Dantas. – Recife, 2014. 66 f. : il. Orientadora: Terezinha Rangel Camara. Dissertação (Mestrado em Botânica) – Universidade Federal Rural de Pernambuco, Departamento de Biologia, Recife, 2014. Inclui referências, anexo(s) e apêndice(s). 1. Micropropagação 2. Dendrobium phalaenopsis 3. Cattleya labiata 4. Superóxido dismutase 5. Ascorbato peroxidase 6. Catalase I. Camara, Terezinha Rangel, orientadora II. Título CDD 581 iv MAIZA DE AZEVEDO DANTAS Aspectos fisiológicos e bioquímicos da morfogênese in vitro de Dendrobium phalaenopsis e Cattleya labiata Dissertação apresentada ao Programa de Pós-Graduação em Botânica (PPGB), da Universidade Federal Rural de Pernambuco, como parte dos requisitos para obtenção do título de Mestre em Botânica. Dissertação defendida e aprovada pela banca examinadora. Orientadora: ________________________________________ Profª. Drª. Terezinha Rangel Camara UFRPE Examinadores: ________________________________________ Profª. Drª. Ana Lúcia Figueiredo Porto Membro Titular/UFRPE ________________________________________ Profª. Drª. Camila Souza Porto Membro Titular/UFRPE ________________________________________ Prof. -
Appendix: Orchid Potting Mixtures - an Abridged Historical Review 1
Appendix: Orchid potting mixtures - An abridged historical review 1 T. J. SHEEHAN Introduction There is little doubt that potting media development over time has been the salvation of orchid growers (Bomba, 1975). When epiphytic orchids were first introduced into England and other European countries in the 18th century growers could not envision plants growing in anything but soil. '"Peat and loam' were good for everything and frequently became the mass murderers of the first generation of epiphytic orchids," Hooker is believed to have said around the end of the 19th century; England had become the graveyard of tropical orchids. Undoubtedly this was in reference to the concern individuals were having over the potting media problems. This problem also drew the attention of such noted individuals as John Lindley and Sir Joseph Paxton, as well as the Gardener's Chronicle, who noted that "The Rule of Thumb" had nothing to say about orchid growing; it was only effective in orchid killing (Bomba 1975). Fortunately, the ingenuity of growers solved the problem as innovative potting mixes evolved over the years. After visiting a number of orchid growing establishments it immediately becomes obvious to any orchid grower, professional or hobbyist, that orchids, both epiphytic and terrestrial, will grow in a wide variety of media. It has often been stated that epiphytic orchids can be grown in any medium except soil as long as watering and fertilization are adjusted to fit the mix being used. Ter restrial orchids seem to thrive in any medium that contains 40% or more organic matter. Reading cultural recommendations from the early days of orchid growing is most interesting and highly recommended. -
Resupination
LANKESTERIANA 7: 95-96. 2003. RESUPINATION JOSEPH ARDITTI Professor Emeritus Department of Developmental and Cell Biology, University of California Irvine, CA 92697-2300, U. S. A. In the great majority of orchids buds are positioned species deresupinate following pollination. Another with the labella uppermost and the gynostemia below interesting characteristic of resupination is that in them. However, flowers are borne with gynostemia some species and hybrids the buds alternate in above the labella which are lowermost. This reversal resupinating clock (CL)- and counter clock (CO)- of positions occurs as a result of a process called wise. In other orchids the flowers may resupinate in resupination which takes place as buds open. In most one direction (CL or CO) only. species the buds turn only to the extent necessary to Surgical experiments by Noes Soediono (owner of place the labellum lowermost which is usually 180º, Flora Sari Orchids in Jakarta, Indonesia), the late Dr. but depending on the position of the inflorescence the Leslie P. Nyman (my postdoctoral fellow at the time) turning can be more or less than that. Some species and myself showed that removal of gynostemium do not resupinate at all and their flowers are often tips, pollinia or stigmas prevent or inhibit resupina- described as being borne upside down. And, the buds tion. Since orchid pollinia contain large amounts of of a few species turn 360º ending up as they started, indoleacetic acid (IAA) these experiments suggested with the labella uppermost. that resupination may be controlled by auxin. This The earliest illustrations of resupination were made possibility was explored by Professor Helen Nair around 1550 by the Swiss naturalist Conrad Gesner (Botany Department, University of Malaya, now (1516-1565), but his Opera Botanica which contains retired) and myself (while on sabbatical leave with them was not published until 1751. -
Crassulacean Acid Metabolism in Epiphytic Orchids: Current Knowledge, Future Perspectives
4 Crassulacean Acid Metabolism in Epiphytic Orchids: Current Knowledge, Future Perspectives Gilberto Barbante Kerbauy, Cassia Ayumi Takahashi, Alejandra Matiz Lopez, Aline Tiemi Matsumura, Leonardo Hamachi, Lucas Macedo Félix, Paula Natália Pereira, Luciano Freschi and Helenice Mercier São Paulo University, Brazil 1. Introduction 1.1 Crassulacean Acid Metabolism (CAM) Crassulacean Acid Metabolism (CAM) is one of three photosynthetic assimilation pathways of atmospheric CO2, together with the photosynthetic pathways C3 and C4 (Silvera et al., 2010a). The CAM is characterized by the temporal separation between CO2 fixation and its assimilation into organic compounds. In CAM plants, CO2 is fixed during the dark period through the action of the enzyme phosphoenolpyruvate carboxylase (PEPC), which uses CO2 for carboxylation of phosphoenolpyruvate (PEP), giving rise to oxaloacetate (OAA). The OAA formed is converted into malate by the action of malate dehydrogenase (MDH). Then, this organic acid is transported to the vacuole along with H+ ions, causing the typical nocturnal acidification of CAM plants. During the light period, the decarboxylation of malate and refixation of the CO2 by the enzyme ribulose bisphosphate carboxylase oxygenase (RUBISCO - C3 cycle) takes place in the cytosol, causing a decrease of acidity in the tissues (Herrera, 2009; Luttge, 2004; Silvera et al., 2010b) (Figure 1). The CAM pathway can be separated into four phases (Luttge, 2004; Osmond, 1978; Silvera et al., 2010b). Phase I is characterized by the opening of stomata during the night, the uptake and subsequent fixation of atmospheric CO2 by PEPC in the cytosol and the formation of organic acids, such as malate. Phase II consists of fixing CO2 by the enzyme RUBISCO and PEPC concurrently, a phase characterized essentially by the decrease in the activity of PEPC and the start of the activity of RUBISCO. -
Intergeneric Classification of Genus Bulbophyllum from Peninsular Malaysia Based on Combined Morphological and Rbcl Sequence Data
Pak. J. Bot., 48(4): 1619-1627, 2016. INTERGENERIC CLASSIFICATION OF GENUS BULBOPHYLLUM FROM PENINSULAR MALAYSIA BASED ON COMBINED MORPHOLOGICAL AND RBCL SEQUENCE DATA SH. HOSSEINI1* AND K. DADKHAH2 1Department of Biological Science and Biotechnology University of Kurdistan, Sanandaj, Iran 2Department of Statistics, Faculty of Science, University of Kurdistan, Sanandaj, Iran *Corresponding author’s e-mail: [email protected] Abstract Bulbophyllum Thou. is largest genus in Orchidaceae family and a well-known plant of tropical area. The present study provides a comparative morphological study of 38 Bulbophyllum spp. as well as molecular sequence analysis of large subunit of rubisco (rbcL), to infer the intergeneric classification for studied taxa of genus Bulbophyllum. Thirty morphological characters were coded in a data matrix, and used in phenetic analysis. Morphological result was strongly consistent with earlier classification, with exception of B. auratum, B. gracillimum, B. mutabile and B. limbatum status. Furthermore Molecular data analysis of rbcL was congruent with morphological data in some aspects. Species interrelationships specified using combination of rbcL sequence data with morphological data. The results revealed close affiliation in 11 sections of Bulbophyllum from Peninsular Malaysia. Consequently, based on this study generic status of sections Cirrhopetalum and Epicrianthes cannot longer be supported, as they are deeply embedded within the genus Bulbophyllum. Key words: Bulbophyllum, Orchidaceae, Peninsular Malaysia, rbcL Introduction Jamil et al., 2014). The structural portion of this study was performed using qualitative characters of rhizome, The largest collection of subtribe Bulbophyllinae pseudobulb, leaf and flower for 38 different species. (Orchidaceae) have been defined as Bulbophyllum, a DNA sequence data from the large subunit of rubisco genus which form a large, pantropical, and poorly studied (rbcL) which produces the carbon dioxide fixing enzyme group of orchids in Peninsular Malaysia. -
Cattleya Walkeriana Gardner)
Vol. 15(46), pp. 2613-2619, 16 November, 2016 DOI: 10.5897/AJB2016.15586 Article Number: A6B8C3A61675 ISSN 1684-5315 African Journal of Biotechnology Copyright © 2016 Author(s) retain the copyright of this article http://www.academicjournals.org/AJB Full Length Research Paper Inbreeding depression in crosses of coerulea clones of Walker’s Cattleya (Cattleya walkeriana Gardner) Miléia Ricci Picolo, Ceci Castilho Custódio, Nelson Barbosa Machado-Neto* Department of Agronomy, Universidade do Oeste Paulista (UNOESTE), Presidente Prudente, São Paulo, Brazil. Received 25 July, 2016; Accepted 21 September, 2016 Orchids are among the most beautiful flowers and endangered due to habitat destruction and over- collection. Cattleya walkeriana is one of the most beautiful flowers joining the small sized plant with medium large and heavily scented flowers. It is widely known and appreciated by its beautiful clones and it has much to offer to breeders because their plants have besides other attributes as small habit and big flowers, many colour variations, form and precocity, becoming flower only four years in ex vitro culture. However, in some of the original places it is becoming a red listed species. Notwithstanding, very little is known about the genetics of these flowers and the variability in the species that is widespread in the Brazilian territory. The aim of this work was to estimate the variability among cultivated materials using the F statistics and to verify if there was inbreeding in plant crosses with similar characteristics, employing as a tool the RAPD simple methodology. The results obtained showed that RAPD was good enough to estimate the variability in C. -
Orchids and Pollination- a Mini Review
ACTA SCIENTIFIC AGRICULTURE (ISSN: 2581-365X) Volume 3 Issue 8 August 2019 Mini Review Orchids and Pollination- A Mini Review Saranjeet Kaur* Department of Applied Sciences, Chandigarh University, Gharuan, Distt. - Mohali, Punjab, India *Corresponding Author: Saranjeet Kaur, Department of Applied Sciences, Chandigarh University, Gharuan, Distt.- Mohali, Punjab, India Received: May 29,2019; Published: July 17, 2019 DOI: 10.31080/ASAG.2019.03.0579 Abstract The orchids are primarily insect pollinated species, yet a variety of pollinators are reported. The pollinators have a considerable role in the evolution of species biodiversity. They exhibit a mutualistic behaviour with orchid species. The orchids have evolved unique to a wide range of pollinators. In this communication, pollination system in orchids is discussed. floral architecture to accomplish pollination successfully. The morphological diversity of orchid flowers reflects several adaptations Keywords: Pollination; euglosine bees; insect pollination; orchids; resupination Introduction To facilitate pollination, the orchid species of diverse habit and habitats have evolved a special mechanism to accomplish polli- nation which is resupination. In this phenomenon twists the ‘lip’ (87.5% approx.) is predominantly pollinated by animals [1]. The highly evolved group of flowering plants i.e. angiosperms below the other two petals of inner whorl twists to 180o, thus, Amongst them, the monocotyledonous family - Orchidaceae, dis- - plays special connection with pollinators due to the structural de- nomenon of resupination is the most characteristic of family orchi- providing a platform for a pollinator to land on the flower. The phe daceae. The orchids species are pollinated by many other members have perianth. The tepals of the outer whorl has three sepals which sign of their flowers.