The Houston Happenings

Total Page:16

File Type:pdf, Size:1020Kb

The Houston Happenings A non profit organization established in 1945, HOS is The Houston Happenings a recipient of the American Orchid Society’s Distinguished Affiliated Societies Service award Volume 50, Issue 3 March 2020 March Program: What to Expect When you Enter a Plant or Create a Display at an Orchid Show By Sarah How are your Orchids coming to like and make their choices tries. If you see a class that you along? Hope you have lots of to award trophies or ribbons. want to enter, talk to Jay Bal- bloom spikes and blossoms in Page 4 of the schedule has a chan at the March 5 meet- Inside This anticipation of the HOS Orchid sample of the form to be filled ing. When I was a newcomer, I Issue: Show and Sale April 4-5, 2020. out to enter each plant for judg- made exhibits several times Several HOS members will pre- ing. If you are unsure how to using the plants of another sent the March program to classify your orchid, there will member who did not have time advise and encourage everyone be an expert at the registration to make an exhibit, because I Presidents Post 1 to share the love of orchids at desk Thursday and Friday to never had enough blooming our annual show and sale. help you. Of course, you will orchids to create a full exhibit. Creating an orchid show need to provide as much infor- This was a great way to get my March Tips 2-3 begins with publishing a sched- mation as you can for your feet wet and have a feel for the ule that lists the events available. plant, especially genera and requirements to make a suc- Holly Miller created this year's parent names. Surely, I do not cessful exhibit. HOS Show 4 schedule and posted it on the need to remind you that each The important thing to re- HOS website: http://www. plant should be groomed to member is this is for fun and Membership 4 houstonorchidsociety.org/ show its best qualities. education. Hoping everyone will assets/show -schedule-for- From the schedule, individu- enjoy the program on Thursday, registration-2020.pdf. The be- als or groups can enter designs March 5 and look forward to Plant Table 5 ginning of the schedule lists all of varying complexity. Remem- working together at Memorial the classes and categories for ber to complete a form to enter City Mall from April 2nd each kind of orchid so the judg- the exhibit for judging. Page 14 through teardown on Sunday Texas Native 6-7 es will be able to compare like lists the classes for design en- afternoon, April 5. Orchid Presidents Post Tamiami IOS 8 City Mall in April and join in on of events in this newsletter for Bill the preparation and camarade- their show dates. rie of putting up exhibits and Not much else to say right AOS Webinars 9 Hello, everyone. participating in a show. While now except Spring is almost you’re there, treat yourself to a here, starting on March 19th, I have to start by saying how new plant or two – you’re wor- the vernal equinox. I hope your Houston Judging 10 impressed I was with the large thy. Jay Balchan, Holly Miller, orchids are waking up and are Center number of new members who and many others have worked spiking after an early, but seems joined the society last month. hard to make this venue and like short winter. I know in my Welcome New Comers, look- show a big hit in the last two orchid tent (it ain’t a green- ing forward to meeting all of years. Let’s make it even bigger house) there are signs every- you soon! Plants on the plant and better in 2020. I appreciate where that Spring is approach- tables at our February meeting everyone’s effort and hope you ing rapidly. My Bletilla striata and were spectacular. Keep bring- will thank them when you have Daffodil in the landscape are in ing in your flowers and showing the opportunity. full bloom two weeks early this off your plants for the rest of us The orchid show season is year. Enjoy it, because in only a to admire. That’s what makes kicking in for many of the other few short months, we’ll be every monthly meeting an or- local societies as well. If you get wishing it were Winter again. chid show and a social event to a chance, take a short road trip enjoy. to visit their shows, meet other Best, Please don’t miss the oppor- orchidphiles and see what they Bill tunity to get out to Memorial are growing. See the schedule Page 2 Volume 50, Issue 3 March Tips - Growing Dendrobiums By Father Ted Last month I talked about Phalaenop- include species such as aphyllum, which sis. This month I have some suggestions loses its leaves and can be purple or about Dendrobium. white; pierardii; and anosmum. The I have been growing them since I latter, curiously, is fragrant although the cannot remember, with some success, name means “no scent”. it blooms in the and quite a few failures. I have mostly concentrated on species and I’ll talk about those first, but also about hybrids, because they tend to be easier to grow. The genus is huge, with over 1000 species, spread throughout eastern Asia, from China through the Philippines and archipelagos West of there, into Austral- Den. thyrsiflorum is also prolific ia and East to some pretty small islands with flowers, but the pseudobulbs are in the Pacific. With my students at the elongated and not “chunky”. Each cane is University of St. Thomas, we performed able to produce one, two, or more inflo- some DNA sampling of 20 or so species rescences. They need more water, and made phylogenetic (parent) trees. strong light, and have to be root-bound The farthest species, geographically and to do well. Spring blooming, this one genetically of them all, comes from the takes up lots of room. islands of New Caledonia and has had a Smaller, but of a most delicious gold- number of names: D. munificum, aka en color is Den. aggregatum (this is the D. muricatum var. munificum, aka trade name. the real name is Dendrobi- Inobulbum munificum. This is a slow um lindleyi or Den. jenkinsii). It is growing, squat, one- or two-leaved spe- shorter, and very compact, unifoliar (one cies that has some peculiarities. First, it leaf), slow growing, but prolific in has many, many flowers. Second, these blooms. There are two drawbacks: it Spring on leafless canes that are pendent. must have a dry period of about three The flowers can be quite large, to 10 cm months: NO WATER; and then, the wide (4”). The center color is quite in- flowers, which bloom all at once and do tense, even in the semi-alba variety, and not last more than two weeks. The pho- it smells faintly like roses to me. These to is of a truly fabulous plant: species are widespread throughout tropi- cal Asia and need copious watering once they start to flower, for about six months to let the new canes grow as long as possible. The leaves will tell you when to slow down and stop by turning flowers fold up at night, an unusual trait. yellow and falling off. If water is not with- Third, the pseudobulbs have long, promi- held, the plant produces only keikis (baby nent hairs that point upwards and give it canes) and no flowers. Pot size is best a strange appearance. They like wet, then kept very small, but baskets are also OK. dry, watering and not too much light, but more than Phalaenopsis. They can bloom anytime, but mine are late Spring. I love my Den. glomeratum (aka Some other species also bloom only sulawelense) and have given away off- after a dry period, like all the shoots to my sister and to friends. It has “nobile” (pronounced NO bil EE). These bunches of striking fuchsia-pink flowers The Houston Happenings Page 3 March Tips (continued) on second year canes and it can be pen- Dockrillia, a synonym. It has pure white My final note is a Dendrobium hybrid dent or erect, depending on conditions flowers in a “frothy” bunch. Mine has not for which I break the rules and let grow (the canes tend to droop quite a but for bloomed like this one, but I have hopes: I out of the pot so the roots are about 4 me). It likes a small dry period of about a just need to wait a bit. It is mounted and ft. long (1.3 m), which I have wrapped month. The flowers are long-lasting - not needs plenty of water, but can take dry around and set in a basket: it has ten as long as D. cuthbertsonii (which we periods in its native climes. The leaves canes, and I finally looked up the parents cannot grow here) - but up to a month! look like pointy, small cucumbers, with a after I had it for ten years: D. Inner Har- long central valley. mony x Uniwai Royale. Since that cross had not been registered in 2017, I named it for my sister, Den. Susan Davis. It will never get an award, but I love it, for sentimental reasons. Sixteen flowers on two inflorescences, and the photo to follow shows it as pink, but in reality, it is much redder. It flowers in late summer.
Recommended publications
  • Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE
    Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE LILIACEAE de Jussieu 1789 (Lily Family) (also see AGAVACEAE, ALLIACEAE, ALSTROEMERIACEAE, AMARYLLIDACEAE, ASPARAGACEAE, COLCHICACEAE, HEMEROCALLIDACEAE, HOSTACEAE, HYACINTHACEAE, HYPOXIDACEAE, MELANTHIACEAE, NARTHECIACEAE, RUSCACEAE, SMILACACEAE, THEMIDACEAE, TOFIELDIACEAE) As here interpreted narrowly, the Liliaceae constitutes about 11 genera and 550 species, of the Northern Hemisphere. There has been much recent investigation and re-interpretation of evidence regarding the upper-level taxonomy of the Liliales, with strong suggestions that the broad Liliaceae recognized by Cronquist (1981) is artificial and polyphyletic. Cronquist (1993) himself concurs, at least to a degree: "we still await a comprehensive reorganization of the lilies into several families more comparable to other recognized families of angiosperms." Dahlgren & Clifford (1982) and Dahlgren, Clifford, & Yeo (1985) synthesized an early phase in the modern revolution of monocot taxonomy. Since then, additional research, especially molecular (Duvall et al. 1993, Chase et al. 1993, Bogler & Simpson 1995, and many others), has strongly validated the general lines (and many details) of Dahlgren's arrangement. The most recent synthesis (Kubitzki 1998a) is followed as the basis for familial and generic taxonomy of the lilies and their relatives (see summary below). References: Angiosperm Phylogeny Group (1998, 2003); Tamura in Kubitzki (1998a). Our “liliaceous” genera (members of orders placed in the Lilianae) are therefore divided as shown below, largely following Kubitzki (1998a) and some more recent molecular analyses. ALISMATALES TOFIELDIACEAE: Pleea, Tofieldia. LILIALES ALSTROEMERIACEAE: Alstroemeria COLCHICACEAE: Colchicum, Uvularia. LILIACEAE: Clintonia, Erythronium, Lilium, Medeola, Prosartes, Streptopus, Tricyrtis, Tulipa. MELANTHIACEAE: Amianthium, Anticlea, Chamaelirium, Helonias, Melanthium, Schoenocaulon, Stenanthium, Veratrum, Toxicoscordion, Trillium, Xerophyllum, Zigadenus.
    [Show full text]
  • 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.
    [Show full text]
  • Native Orchids of Oklahoma Dr. Lawrence K. Magrath Curator-USAO
    Oklahoma Native Plant Record 39 Volume 1, Number 1, December 2001 Native Orchids of Oklahoma Dr. Lawrence K. Magrath Curator-USAO (OCLA) Herbarium Chickasha, OK 73018-5358 As of the publication of this paper Oklahoma is known to have orchids of 33 species in 18 genera, which compares to 20 species and 11 genera reported by Waterfall (1969). Four of the 33 species are possibly extinct in the state based on current survey work. The greatest concentration of orchid species is in the southeastern corner of the state (Atoka, Bryan, Choctaw, LeFlore, McCurtain and Pushmataha Counties). INTRODUCTION Since the time of Confucius (551-479 BCE) who mentioned lan in his writings, "acquaintance with The family Orchidaceae is the largest of the good men was like entering a room full of lan or families of flowering plants with somewhere between fragrant orchids" (Withner, 1959), orchids have been 25,000 and 35,000 species, with new species important in many facets of Chinese life including continually being described. There are also literature, painting, horticulture, and not least, numerous natural and artificial hybrids. The only medicine". They are mentioned in the materia place where orchids are not known to occur is medica, “Sheng nung pen ts'ao ching”, tracing back Antarctica. to the legendary emperor Sheng Nung (ca. 28th Orchids fascinate us because of the century BCE). The term "lan hua" in early Chinese seemingly infinite combinations of colors and forms records refers to species of the genus Cymbidium that are found in orchid flowers from the Arctic to (Withner, 1959), most likely Cymbidium the tropical rain forests.
    [Show full text]
  • Phylogeny, Character Evolution and the Systematics of Psilochilus (Triphoreae)
    THE PRIMITIVE EPIDENDROIDEAE (ORCHIDACEAE): PHYLOGENY, CHARACTER EVOLUTION AND THE SYSTEMATICS OF PSILOCHILUS (TRIPHOREAE) A Dissertation Presented in Partial Fulfillment of the Requirements for The Degree Doctor of Philosophy in the Graduate School of the Ohio State University By Erik Paul Rothacker, M.Sc. ***** The Ohio State University 2007 Doctoral Dissertation Committee: Approved by Dr. John V. Freudenstein, Adviser Dr. John Wenzel ________________________________ Dr. Andrea Wolfe Adviser Evolution, Ecology and Organismal Biology Graduate Program COPYRIGHT ERIK PAUL ROTHACKER 2007 ABSTRACT Considering the significance of the basal Epidendroideae in understanding patterns of morphological evolution within the subfamily, it is surprising that no fully resolved hypothesis of historical relationships has been presented for these orchids. This is the first study to improve both taxon and character sampling. The phylogenetic study of the basal Epidendroideae consisted of two components, molecular and morphological. A molecular phylogeny using three loci representing each of the plant genomes including gap characters is presented for the basal Epidendroideae. Here we find Neottieae sister to Palmorchis at the base of the Epidendroideae, followed by Triphoreae. Tropidieae and Sobralieae form a clade, however the relationship between these, Nervilieae and the advanced Epidendroids has not been resolved. A morphological matrix of 40 taxa and 30 characters was constructed and a phylogenetic analysis was performed. The results support many of the traditional views of tribal composition, but do not fully resolve relationships among many of the tribes. A robust hypothesis of relationships is presented based on the results of a total evidence analysis using three molecular loci, gap characters and morphology. Palmorchis is placed at the base of the tree, sister to Neottieae, followed successively by Triphoreae sister to Epipogium, then Sobralieae.
    [Show full text]
  • Division, Usually Consists (Viscidium)
    Acta Bolanica Neerlandica 8 (1959) 338-355 The Different Structure of the Rostellum in Ophrydeae and Neottieae P. Vermeulen (Hugo de Vries-Laboratorium, Amsterdam) (received March 25th, 1959) rostellum is forms viscid The in orchids the organ that the liquid which makes it possible for the pollinia to stick to the bodies of visiting insects. The then taken and be pollinia are along may deposited the wholly or partly on stigma of another flower. The rostellum, how- ever, does not occur in all orchids, viz. not in the Cypripedioideae which do not It is in (Diandrae), possess pollinia. present practically all the Orchioideae (Monandrae), on the other hand, but often has very different structures. In the group including Ophrys, Platanthera, Haben- aria it forms the viscid discs and in the it etc., (viscidia), other groups usually consists of one single gland (viscidium), such as in Goodyera, it Spiranthes and Epidendrum, whereas the simple gland, as we find in Vanda and related is characterized i.e. genera, moreover, by a stipes, a tissue tape of the column formin ghe connection between the viscid disc and the pollinia. § 1. The division in the orchioideae When gradually a great number of orchids became known and when little by little, the pioneering work of Lindley (1853) made it of the Orchidaceae Reichenbach possible to compile a survey (1868) was the first to stress the differences between the Ophrydeae (Anthera cum columna connata) on the one hand, where the anther is inter- with the and the demum grown column, Operculatae (Anthera a in which columna libera, secedens saltern) on the other hand, the anther is completely free or is fixed only at the base (1868 p.
    [Show full text]
  • Annotated Checklist of the Vascular Plants of the Washington - Baltimore Area
    Annotated Checklist of the Vascular Plants of the Washington - Baltimore Area Part II Monocotyledons Stanwyn G. Shetler Sylvia Stone Orli Botany Section, Department of Systematic Biology National Museum of Natural History Smithsonian Institution, Washington, DC 20560-0166 MAP OF THE CHECKLIST AREA Annotated Checklist of the Vascular Plants of the Washington - Baltimore Area Part II Monocotyledons by Stanwyn G. Shetler and Sylvia Stone Orli Department of Systematic Biology Botany Section National Museum of Natural History 2002 Botany Section, Department of Systematic Biology National Museum of Natural History Smithsonian Institution, Washington, DC 20560-0166 Cover illustration of Canada or nodding wild rye (Elymus canadensis L.) from Manual of the Grasses of the United States by A. S. Hitchcock, revised by Agnes Chase (1951). iii PREFACE The first part of our Annotated Checklist, covering the 2001 species of Ferns, Fern Allies, Gymnosperms, and Dicotyledons native or naturalized in the Washington-Baltimore Area, was published in March 2000. Part II covers the Monocotyledons and completes the preliminary edition of the Checklist, which we hope will prove useful not only in itself but also as a first step toward a new manual for the identification of the Area’s flora. Such a manual is needed to replace the long- outdated and out-of-print Flora of the District of Columbia and Vicinity of Hitchcock and Standley, published in 1919. In the preparation of this part, as with Part I, Shetler has been responsible for the taxonomy and nomenclature and Orli for the database. As with the first part, we are distributing this second part in preliminary form, so that it can be used, criticized, and updated while the two parts are being readied for publication as a single volume.
    [Show full text]
  • Phylogenetic Analysis of Neottia Japonica (Orchidaceae) Based on ITS and Matk Regions Ji-Hyeon SO and Nam-Sook LEE1*
    Korean J. Pl. Taxon. 50(4): 385−394 (2020) pISSN 1225-8318 eISSN 2466-1546 https://doi.org/10.11110/kjpt.2020.50.4.385 Korean Journal of RESEARCH ARTICLE Plant Taxonomy Phylogenetic analysis of Neottia japonica (Orchidaceae) based on ITS and matK regions Ji-Hyeon SO and Nam-Sook LEE1* Interdisciplinary Program of EcoCreative, Ewha Womans University, Seoul 03760, Korea 1Department of Life Science, College of Natural Science, Ewha Womans University, Seoul 03760, Korea (Received 7 September 2020; Revised 25 November 2020; Accepted 22 December 2020) ABSTRACT: To elucidate the molecular phylogeny of Neottia japonica, which is a terrestrial orchid distributed in East Asia, the internal transcribed spacer (ITS) of nuclear DNA and the matK of chloroplast DNA were used. A total 22 species of 69 accessions for ITS and 21 species of 114 accessions for matK phylogeny were analyzed with the max- imum parsimony and Bayesian methods. In addition, we sought to establish a correlation between the distribution, morphology of the auricles and genetic association of N. japonica with phylogenetic data. The phylogenetic results suggest that N. japonica is monophyletic and a sister to N. suzukii in terms of the ITS phylogeny, while it is para- phyletic with N. suzukii in terms of the matK phylogeny. N. japonica and N. suzukii show similar morphologies of the lip and column, they both flower in April, and they are both distributed sympatrically in Taiwan. Therefore, it appears to be clear that N. japonica and N. suzukii are close taxa within Neottia, although there is incongruence between the nrDNA and cpDNA phylogenies of N.
    [Show full text]
  • Temporal Variation in Community Composition of Root Associated Endophytic Fungi and Carbon and Nitrogen Stable Isotope Abundance in Two Bletilla Species (Orchidaceae)
    plants Article Temporal Variation in Community Composition of Root Associated Endophytic Fungi and Carbon and Nitrogen Stable Isotope Abundance in Two Bletilla Species (Orchidaceae) Xinhua Zeng 1, Haixin Diao 1, Ziyi Ni 1, Li Shao 1, Kai Jiang 1 , Chao Hu 1, Qingjun Huang 2 and Weichang Huang 1,3,* 1 Shanghai Chenshan Plant Science Research Center, Chinese Academy of Sciences, Chenshan Botanical Garden, Shanghai 201620, China; [email protected] (X.Z.); [email protected] (H.D.); [email protected] (Z.N.); [email protected] (L.S.); [email protected] (K.J.); [email protected] (C.H.) 2 Shanghai Institute of Technology, Shanghai 201418, China; [email protected] 3 College of Landscape Architecture, Fujian Agriculture and Forestry University, Fuzhou 350002, China * Correspondence: [email protected] Abstract: Mycorrhizae are an important energy source for orchids that may replace or supplement photosynthesis. Most mature orchids rely on mycorrhizae throughout their life cycles. However, little is known about temporal variation in root endophytic fungal diversity and their trophic functions throughout whole growth periods of the orchids. In this study, the community composition of root endophytic fungi and trophic relationships between root endophytic fungi and orchids were investigated in Bletilla striata and B. ochracea at different phenological stages using stable isotope natural abundance analysis combined with molecular identification analysis. We identified 467 OTUs assigned to root-associated fungal endophytes, which belonged to 25 orders in 10 phyla. Most of these OTUs were assigned to saprotroph (143 OTUs), pathotroph-saprotroph (63 OTUs) and pathotroph- saprotroph-symbiotroph (18 OTUs) using FunGuild database. Among these OTUs, about 54 OTUs Citation: Zeng, X.; Diao, H.; Ni, Z.; could be considered as putative species of orchid mycorrhizal fungi (OMF).
    [Show full text]
  • Lineage-Specific Reductions of Plastid Genomes in an Orchid Tribe with Partially and Fully Mycoheterotrophic Species
    GBE Lineage-Specific Reductions of Plastid Genomes in an Orchid Tribe with Partially and Fully Mycoheterotrophic Species Yan-Lei Feng1,9,y, Susann Wicke2,y,Jian-WuLi3,YuHan4, Choun-Sea Lin5, De-Zhu Li6, Ting-Ting Zhou1,9, Wei-Chang Huang7,Lu-QiHuang8, and Xiao-Hua Jin1,* 1State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing, China 2Institute for Evolution and Biodiversity, University of Muenster, Germany 3Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Menglun Township, Mengla County, Yunnan, China 4Nanchang University, Jiangxi, China 5Agricultural Biotechnology Research Center, Academia Sinica, Taipei, Taiwan 6Key Laboratory of Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, China 7Chenshan Shanghai Botanical Garden, Shanghai, Songjiang, China 8National Resource Centre for Chinese Materia Medica, China Academy of Chinese Medical Science, Beijing, China 9University of Chinese Academy of Sciences, Beijing, China yThese authors contributed equally to this work. *Corresponding author: E-mail: [email protected]. Accepted: June 8, 2016 Data deposition: This project has been deposited at NCBI under the accession number KU551262-Ku551272. Abstract The plastid genome (plastome) of heterotrophic plants like mycoheterotrophs and parasites shows massive gene losses in conse- quence to the relaxation of functional constraints on photosynthesis. To understand the patterns of this convergent plastome reduction syndrome in heterotrophic plants, we studied 12 closely related orchids of three different lifeforms from the tribe Neottieae (Orchidaceae). We employ a comparative genomics approach to examine structural and selectional changes in plastomes within Neottieae. Both leafy and leafless heterotrophic species have functionally reduced plastid genome.
    [Show full text]
  • Newsletter 2010
    The UniversiTy of georgia franklin college of arts and sciences a DeparTmenT of planT Biology newsletter JUne 2010 monocot Tree of life The yucca flower is not your grandfather’s plant systematics insect pollinated by the yucca moth. ystematists have tried to understand nuclear genes for over fifty species. These how species are related to each data should allow us to resolve relation- other since Theophrastus, the father ships among all monocot families and Sof botany, lived between the third and gain new insights into the evolution of ing. “As a postdoc I started studying the second century BC. Down through the morphological characteristics, life history amazing obligate pollination mutualism ages, they have depended on comparing traits and genome structure throughout between yuccas and yucca moths. Yucca flower structure, stems and leaves to sort monocot history.” moths have specialized mouthparts they out relationships. Both Wendy Zomlefer, another Plant use to collect yucca pollen and actively In the last 20 years plant system- Biology faculty member participating in deposit it on yucca stigmas. This is not atists have added a dynamic tool to their the Monocot Tree of Life project, and your typical insect pollination sys- toolkit—DNA sequencing. Thanks to the Jim, got hooked on studying non-grass tem! Female yucca moths place their egg recent development of powerful high- monocot species, in the orders Liliales in yucca ovaries before walking up the through put technologies, also known as and Asparagales, respectively. Wendy’s pistil and actively jamming pollen into “next generation” technologies, research- undergraduate days in Vermont helped the bowl-shaped yucca stigmas.
    [Show full text]
  • Systematics, Phylogeography, Fungal Associations, and Photosynthesis
    Systematics, Phylogeography, Fungal Associations, and Photosynthesis Gene Evolution in the Fully Mycoheterotrophic Corallorhiza striata Species Complex (Orchidaceae: Epidendroideae) Dissertation Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of the Ohio State University By Craig Francis Barrett, M. S. Evolution, Ecology, and Organismal Biology ***** The Ohio State University 2010 Dissertation Committee: Dr. John V. Freudenstein, Advisor Dr. John W. Wenzel Dr. Andrea D. Wolfe Copyright by Craig Francis Barrett 2010 ABSTRACT Corallorhiza is a genus of obligately mycoheterotrophic (fungus-eating) orchids that presents a unique opportunity to study phylogeography, taxonomy, fungal host specificity, and photosynthesis gene evolution. The photosysnthesis gene rbcL was sequenced for nearly all members of the genus Corallorhiza; evidence for pseudogene formation was found in both the C. striata and C. maculata complexes, suggesting multiple independent transitions to complete heterotrophy. Corallorhiza may serve as an exemplary system in which to study the plastid genomic consequences of full mycoheterotrophy due to relaxed selection on photosynthetic apparatus. Corallorhiza striata is a highly variable species complex distributed from Mexico to Canada. In an investigation of molecular and morphological variation, four plastid DNA clades were identified, displaying statistically significant differences in floral morphology. The biogeography of C. striata is more complex than previously hypothesized, with two main plastid lineages present in both Mexico and northern North America. These findings add to a growing body of phylogeographic data on organisms sharing this common distribution. To investigate fungal host specificity in the C. striata complex, I sequenced plastid DNA for orchids and nuclear DNA for fungi (n=107 individuals), and found that ii the four plastid clades associate with divergent sets of ectomycorrhizal fungi; all within a single, variable species, Tomentella fuscocinerea.
    [Show full text]
  • Molecular Phylogenetic Study of the Tribe Tropidieae (Orchidaceae, Epidendroideae) with Taxonomic and Evolutionary Implications
    A peer-reviewed open-access journal PhytoKeys 140: 11–22 (2020) Molecular phylogenetic study of Tropidieae 11 doi: 10.3897/phytokeys.140.46842 RESEARCH ARTICLE http://phytokeys.pensoft.net Launched to accelerate biodiversity research Molecular phylogenetic study of the tribe Tropidieae (Orchidaceae, Epidendroideae) with taxonomic and evolutionary implications Izai A.B. Sabino Kikuchi1, Paul J.A. Keßler1, André Schuiteman2, Jin Murata3, Tetsuo Ohi-Toma3, Tomohisa Yukawa4, Hirokazu Tsukaya5,6 1 Universiteit Leiden, Hortus botanicus Leiden, PO Box 9500, Leiden, 2300 RA, The Netherlands2 Science Directorate, Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AB, UK 3 Botanical Gardens, Graduate School of Science, The University of Tokyo, 3-7-1 Hakusan, Bunkyo-ku, Tokyo, 112-0001, Japan4 Tsukuba Botanical Garden, National Science Museum, 4-1-1 Amakubo, Tsukuba, 305-0005, Japan 5 Department of Biological Sciences, Faculty of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan 6 Bio-Next Project, Okazaki Institute for Integrative Bioscience, National Institutes of Natural Sciences, Yamate Build. #3, 5-1, Higashiyama, Myodaiji, Okazaki, Aichi, 444-8787, Japan Corresponding author: Izai A. B. Sabino Kikuchi ([email protected]) Academic editor: M. Simo-Droissart | Received 26 September 2019 | Accepted 18 December 2019 | Published 19 February 2020 Citation: Sabino Kikuchi IAB, Keßler PJA, Schuiteman A, Murata J, Ohi-Toma T, Yukawa T, Tsukaya H (2020) Molecular phylogenetic study of the tribe Tropidieae (Orchidaceae, Epidendroideae) with taxonomic and evolutionary implications. PhytoKeys 140: 11–22. https://doi.org/10.3897/phytokeys.140.46842 Abstract The orchid tribe Tropidieae comprises three genera,Tropidia , Corymborkis and Kalimantanorchis.
    [Show full text]