The Gift of Bromeliads
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Leaf Anatomy and C02 Recycling During Crassulacean Acid Metabolism in Twelve Epiphytic Species of Tillandsia (Bromeliaceae)
Int. J. Plant Sci. 154(1): 100-106. 1993. © 1993 by The University of Chicago. All rights reserved. 1058-5893/93/5401 -0010502.00 LEAF ANATOMY AND C02 RECYCLING DURING CRASSULACEAN ACID METABOLISM IN TWELVE EPIPHYTIC SPECIES OF TILLANDSIA (BROMELIACEAE) VALERIE S. LOESCHEN,* CRAIG E. MARTIN,' * MARIAN SMITH,t AND SUZANNE L. EDERf •Department of Botany, University of Kansas, Lawrence, Kansas 66045-2106; and t Department of Biological Sciences, Southern Illinois University, Edwardsville, Illinois 62026-1651 The relationship between leaf anatomy, specifically the percent of leaf volume occupied by water- storage parenchyma (hydrenchyma), and the contribution of respiratory C02 during Crassulacean acid metabolism (CAM) was investigated in 12 epiphytic species of Tillandsia. It has been postulated that the hydrenchyma, which contributes to C02 exchange through respiration only, may be causally related to the recently observed phenomenon of C02 recycling during CAM. Among the 12 species of Tillandsia, leaves of T. usneoides and T. bergeri exhibited 0% hydrenchyma, while the hydrenchyma in the other species ranged from 2.9% to 53% of leaf cross-sectional area. Diurnal malate fluctuation and nighttime atmospheric C02 uptake were measured in at least four individuals of each species. A significant excess of diurnal malate fluctuation as compared with atmospheric C02 absorbed overnight was observed only in T. schiedeana. This species had an intermediate proportion (30%) of hydrenchyma in its leaves. Results of this study do not support the hypothesis that C02 recycling during CAM may reflect respiratory contributions of C02 from the tissue hydrenchyma. Introduction tions continue through fixation of internally re• leased, respired C02 (Szarek et al. -
Spanish Moss and Ball Moss 1
FOR52 Spanish Moss and Ball Moss 1 Nancy P. Arny2 Spanish moss (Tillandsia usneoides) and ball Bromeliads moss (T. recurvata) are common elements of the Florida landscape. They are two of Florida's native Like almost all members of the Bromeliaceae, members of the Bromeliaceae, also known as the Spanish moss and ball moss are perennial herbs. This pineapple family. This family includes species as means they do not have permanent woody stems diverse as pineapples, Spanish moss and a above ground, but that individual plants persist for carnivorous relative native to Australia. Bromeliads years and will reproduce without human intervention. are members of the plant division Like many other bromeliads, these plants are Magnoliophyta--the flowering plants. While most epiphytes or "air plants". This indicates that they do Floridians are at least vaguely familiar with Spanish not require soil to root in, but can survive and thrive moss, many have never seen it flower and may be growing above the ground hanging on branches of surprised at the beauty of its delicate blossom. Of trees or other structures. They are not parasites. course, the fact that both Spanish moss and ball moss Without soil as a source of nutrients, these plants produce flowers is proof that they are not truly have evolved the capacity to make use of minerals mosses at all. dissolved in the water which flows across leaves and down branches. This fact sheet will help the reader to distinguish between the two common Tillandsias . It also Spanish moss plants appear to vary in mineral provides basic information on the biology and content and it has been proven that they gain a ecology of these fascinating plants and provides significant portion of their nutrients from stem recommendations for their management in the home run-off from the trees on which they are anchored. -
Diversity and Evolution of Monocots
Commelinids 4 main groups: Diversity and Evolution • Acorales - sister to all monocots • Alismatids of Monocots – inc. Aroids - jack in the pulpit • Lilioids (lilies, orchids, yams) – non-monophyletic . spiderworts, bananas, pineapples . – petaloid • Commelinids – Arecales – palms – Commelinales – spiderwort – Zingiberales –banana – Poales – pineapple – grasses & sedges Commelinids Commelinales + Zingiberales • theme: reduction of flower, loss of nectar, loss of zoophily, evolution of • 2 closely related tropical orders bracts • primarily nectar bearing but with losses • bracted inflorescences grass pickeral weed pickeral weed spiderwort heliconia nectar pollen only bracts rapatead bromeliad Commelinaceae - spiderwort Commelinaceae - spiderwort Family of small herbs with succulent stems, stems jointed; leaves sheathing. Family does not produce Inflorescence often bracted nectar, but showy flowers for insect pollen gathering. Rhoeo - Moses in a cradle Commelina erecta - Erect dayflower Tradescantia ohiensis - spiderwort Tradescantia ohiensis - spiderwort Commelinaceae - spiderwort Commelinaceae - spiderwort Flowers actinomorphic or • species rich in pantropics, CA 3 CO 3 A 6 G (3) zygomorphic especially Africa • floral diversity is enormous Commelina communis - day flower Tradescantia ohiensis - spiderwort Pontederiaceae - pickerel weed Pontederiaceae - pickerel weed Aquatic family of emergents or floaters. Pickerel weed has glossy heart-shaped leaves, Water hyacinth (Eichhornia) from superficially like Sagittaria but without net venation. -
Generic Classification of Amaryllidaceae Tribe Hippeastreae Nicolás García,1 Alan W
TAXON 2019 García & al. • Genera of Hippeastreae SYSTEMATICS AND PHYLOGENY Generic classification of Amaryllidaceae tribe Hippeastreae Nicolás García,1 Alan W. Meerow,2 Silvia Arroyo-Leuenberger,3 Renata S. Oliveira,4 Julie H. Dutilh,4 Pamela S. Soltis5 & Walter S. Judd5 1 Herbario EIF & Laboratorio de Sistemática y Evolución de Plantas, Facultad de Ciencias Forestales y de la Conservación de la Naturaleza, Universidad de Chile, Av. Santa Rosa 11315, La Pintana, Santiago, Chile 2 USDA-ARS-SHRS, National Germplasm Repository, 13601 Old Cutler Rd., Miami, Florida 33158, U.S.A. 3 Instituto de Botánica Darwinion, Labardén 200, CC 22, B1642HYD, San Isidro, Buenos Aires, Argentina 4 Departamento de Biologia Vegetal, Instituto de Biologia, Universidade Estadual de Campinas, Postal Code 6109, 13083-970 Campinas, SP, Brazil 5 Florida Museum of Natural History, University of Florida, Gainesville, Florida 32611, U.S.A. Address for correspondence: Nicolás García, [email protected] DOI https://doi.org/10.1002/tax.12062 Abstract A robust generic classification for Amaryllidaceae has remained elusive mainly due to the lack of unequivocal diagnostic characters, a consequence of highly canalized variation and a deeply reticulated evolutionary history. A consensus classification is pro- posed here, based on recent molecular phylogenetic studies, morphological and cytogenetic variation, and accounting for secondary criteria of classification, such as nomenclatural stability. Using the latest sutribal classification of Hippeastreae (Hippeastrinae and Traubiinae) as a foundation, we propose the recognition of six genera, namely Eremolirion gen. nov., Hippeastrum, Phycella s.l., Rhodolirium s.str., Traubia, and Zephyranthes s.l. A subgeneric classification is suggested for Hippeastrum and Zephyranthes to denote putative subclades. -
Bromeliads Bromeliads Are a Family of Plants (Bromeliaceae, the Pineapple Family) Native to Tropical North and South America
A Horticulture Information article from the Wisconsin Master Gardener website, posted 19 March 2012 Bromeliads Bromeliads are a family of plants (Bromeliaceae, the pineapple family) native to tropical North and South America. Europeans fi rst found out about bromeliads on Columbus’ second trip to the New World in 1493, where the pineapple (Ananas sp.) was being cultivated by the Carib tribe in the West Indies. The commercial pineapple (Ananas comosus) is native to southern Brazil and Paraguay. After the colonization of the New World it was rapidly transported to all areas of the tropics, and now is widely grown in tropical and sub- tropical areas. The only A collection of bromeliads placed on a tree at Costa Flores, Costa Rica. bromeliad to occur north of the tropics is Spanish “moss” (Tillandsia usneoides). It is neither Spanish nor a moss, but an epiphytic bromeliad. It doesn’t look much like a typical Commercial pineapple, Ananas comosus, bromeliad, though, with its long scaly stems and reduced in the fi eld. fl owers. Bromeliads are monocots, many of which, like their grass relatives, have a special form of photosynthesis that uses a variation of the more usual biochemical pathways to allow them to use water more effi ciently. Even though they come from the tropics, this helps those that are epiphytes contend with life in the treetops where there is limited water and a real danger of drying out. There are about 2500 species Many bromeliads are tropical and several thousand hybrids epiphytes. and cultivars. Many have brightly colored leaves, fl owers or fruit, and range in size from moss-like species of Tillandsia to the enormous Puya raimondii from the Andes which produces a fl owering stem up to 15 feet tall. -
Water Relations of Bromeliaceae in Their Evolutionary Context
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Apollo Botanical Journal of the Linnean Society, 2016, 181, 415–440. With 2 figures Think tank: water relations of Bromeliaceae in their evolutionary context JAMIE MALES* Department of Plant Sciences, University of Cambridge, Downing Street, Cambridge CB2 3EA, UK Received 31 July 2015; revised 28 February 2016; accepted for publication 1 March 2016 Water relations represent a pivotal nexus in plant biology due to the multiplicity of functions affected by water status. Hydraulic properties of plant parts are therefore likely to be relevant to evolutionary trends in many taxa. Bromeliaceae encompass a wealth of morphological, physiological and ecological variations and the geographical and bioclimatic range of the family is also extensive. The diversification of bromeliad lineages is known to be correlated with the origins of a suite of key innovations, many of which relate directly or indirectly to water relations. However, little information is known regarding the role of change in morphoanatomical and hydraulic traits in the evolutionary origins of the classical ecophysiological functional types in Bromeliaceae or how this role relates to the diversification of specific lineages. In this paper, I present a synthesis of the current knowledge on bromeliad water relations and a qualitative model of the evolution of relevant traits in the context of the functional types. I use this model to introduce a manifesto for a new research programme on the integrative biology and evolution of bromeliad water-use strategies. The need for a wide-ranging survey of morphoanatomical and hydraulic traits across Bromeliaceae is stressed, as this would provide extensive insight into structure– function relationships of relevance to the evolutionary history of bromeliads and, more generally, to the evolutionary physiology of flowering plants. -
Aechmea Information Compiled by Theresa M
Aechmea Information compiled by Theresa M. Bert, Ph.D. (corresponding author) and Harry E. Luther, Director, Mulford B. Foster Bromeliad Identification Center (last update: January 2005) Welcome to the Aechmea species list. All taxonomic entities for the genus Aechmea listed in Luther (2004) & new species & taxonomic revisions since that publication up to September 2004 are included here. The information provided for each taxon is summarized from the references & citations provided at the end of the list. In the table, the citations are denoted by superscripted numbers. This information is not all-inclusive of everything that is known about each species, but much information is included. We did not include information on citings during personal expeditions unless they were documented in the literature & also provided unique information on the biology, ecology, or taxonomy of the species. Nor did we include information on cultivation. This is a dynamic table. As authoritative information becomes available, we will update this table. We also invite input. If you know of a well-documented fact about a species in this list, please provide the corresponding author with the information & the literature citation in which that information appears. (We reserve the right to accept or deny inclusion of any information provided to us.) We also welcome your thoughts on the type of information that should be included in this list. Blank fields denote no information is available. All currently recognized taxonomic entities of each species are listed, including subspecies, varieties, & forms. When the lower taxonomic level of these plants is the same as the species, only the species name is given (e.g., Aechmea distichantha var. -
The Genus Guzmania (Bromeliaceae) in Venezuela
The genus Guzmania (Bromeliaceae) in Venezuela Compiled by Yuribia Vivas Fundación Instituto Botánico de Venezuela Bruce Holst & Harry Luther Marie Selby Botanical Gardens The genus Guzmania was described by Hipólito Ruiz and José Pavón in 1802 in the "Flora Peruviana et Chilensis." The type species is Guzmania tricolor Ruiz & Pav. The name honors Spanish naturalist Anastasio Guzmán, a student of South American plants and animals (Grant & Zijlstra 1998). Species of Guzmania are distributed from the southern USA (Florida) and Mexico to Brazil and Peru, including the Most species of Guzmania are found in cloud forests at middle elevations. Antilles; they are largely absent from lowland Amazonia. Photograph by Yuribia Vivas. Figure modified from Smith & Downs, Flora Neotropica. Guzmania is placed in the subfamily Tillandsioideae, and is distinguished from other members of the subfamily (Vriesea,Tillandsia, Catopsis, Racinaea, Alcantarea, Mezobromelia, and Werauhia) by having polystichously arranged flowers (that is, arranged in many planes on the inflorescence axis), white, whitish, yellow, or greenish petals that lack nectar scales, and having generally reddish brown-colored seeds. In general aspect, Guzmania is difficult to distinguish from Mezobromelia since both are polystichously flowered and may have similar color schemes, but the presence of nectar scales in Mezobromelia and absence inGuzmania separates them. Approximately 200 species and 17 varieties of Guzmania are known, making it the third largest genus in the subfamily, after Tillandsia and Vriesea. The table below is a listing of Guzmania in Venezuela, with synonymy, types, phenology, and distribution. Column two contains photographs of live plants and the third column, type specimens. Click on the photos for enlarged images. -
Ball Moss Tillandsia Recurvata
Ball Moss Tillandsia recurvata Like Spanish moss, ball moss is an epiphyte and belongs to family Bromeliaceae. Ball moss [Tillandsia recurvata (L.) L], or an air plant, is not a true moss but rather is a small flowering plant. It is neither a pathogen nor a parasite. During the past couple of years, ball moss has increas- ingly been colonizing trees and shrubs, including oaks, pines, magnolias, crape myrtles, Bradford pears and others, on the Louisiana State University campus and surrounding areas in Baton Rouge. In addition to trees and shrubs, ball moss can attach itself to fences, electric poles and other physical structures with the help of pseudo-roots. Ball moss uses trees or plants as surfaces to grow on but does not derive any nutrients or water from them. Ball moss is a true plant and can prepare its own food by using water vapors and nutrient from the environment. Extending from Georgia to Arizona and Mexico, ball moss thrives in high humidity and low intensity sunlight environments. Unlike loose, fibrous Spanish moss, ball moss grows in a compact shape of a ball ranging in size from a Figure 1. Young ball moss plant. golf ball to a soccer ball. Ball moss leaves are narrow and grayish-green, with pointed tips that curve outward from the center of the ball. It gets its mosslike appearance from the trichomes present on the leaves. Blue to violet flowers emerge on long central stems during spring. Ball moss spreads to new locations both through wind-dispersed seeds and movement of small vegetative parts of the plant. -
Ectopic Expression of the Aechmea Fasciata APETALA2 Gene Afap2-2
Plant Physiology and Biochemistry 139 (2019) 642–650 Contents lists available at ScienceDirect Plant Physiology and Biochemistry journal homepage: www.elsevier.com/locate/plaphy Research article Ectopic expression of the Aechmea fasciata APETALA2 gene AfAP2-2 reduces T seed size and delays flowering in Arabidopsis Ming Leia,b,c,d,e, Zhi-ying Lia,c,d,e, Jia-bin Wanga,c,d,e, Yun-liu Fua,c,d,e, Li Xua,c,d,e, a Institute of Tropical Crop Genetic Resources, Chinese Academy of Tropical Agricultural Sciences, Danzhou, 571737, China b Guangxi Key Laboratory of Medicinal Resources Protection and Genetic Improvement, Guangxi Botanical Garden of Medicinal Plants, Nanning, Guangxi, 530023, China c Key Laboratory of Crop Gene Resources and Germplasm Enhancement in Southern China, Danzhou, 571737, China d Key Laboratory of Tropical Crops Germplasm Resources Genetic Improvement and Innovation, Danzhou, 571737, China e Mid Tropical Crop Gene Bank of National Crop Resources, Danzhou, 571737, China ARTICLE INFO ABSTRACT Keywords: The Bromeliaceae family, which is distributed pantropically, is one of the most morphologically diverse families. Aechmea fasciata Except for the edible pineapple (Ananas comosus), the vast majority of bromeliads cultivated worldwide are APETALA2 appreciated mainly for their ornamental value. As subtropical and tropical flowering plants, these bromeliads, Transcriptional activator among with Aechmea fasciata, have significant economic importance. However, the molecular mechanism of Flowering flowering in bromeliads remains unrevealed. In this study, an APETALA2 (AP2) homologue, AfAP2-2, which Seed size belongs to the AP2/ethylene response element binding protein (AP2/EREBP) transcription factor superfamily, Bromeliad was identified in A. fasciata. AfAP2-2 contains two conserved AP2 domains and is a nuclear-localized transac- tivator. -
May 2007 [email protected]
CALOOSAHATCHEE BROMELIAD SOCIETY’s CALOOSAHATCHEE MERISTEM 3836 Hidden Acres Circle N North Fort Myers Fl 33903 (239) 997-2237 May 2007 [email protected] Neoregelia ‘Joe’s Mauve’ (A Hummel hybrid named for Joe Bailey) Joe and Peggy Bailey , while living in Fort Myers (Photo by Ann Collings) CALOOSAHATCHEE BROMELIAD SOCIETY OFFICERS EXECUTIVE COMMITTEE PRESIDENT Steve Hoppin ([email protected]) VICE-PRESIDENT Tom Foley ([email protected]) SECRETARY Chuck Ray ([email protected]) TREASURER Betty Ann Prevatt ([email protected]) PAST-PRESIDENT Dianne Molnar ([email protected]) STANDING COMMITTEES CHAIRPERSONS NEWSLETTER EDITOR Larry Giroux ([email protected]) FALL SHOW CHAIR Steve Hoppin ([email protected]) FALL SALES CHAIR Brian Weber ([email protected]) FALL SHOW Co-CHAIR Betty Ann Prevatt ([email protected]) PROGRAM CHAIRPERSONS Debbie Booker/Tom Foley ([email protected]) WORKSHOP CHAIRPERSON Eleanor Kinzie SPECIAL PROJECTS Deb Booker/Tom Foley Senior CBS FCBS Rep. Vicky Chirnside ([email protected]) Co-Junior CBS FCBS Reps. Debbie Booker & Tom Foley Alternate CBS FCBS Rep. Dale Kammerlohr ([email protected]) OTHER COMMITTEES AUDIO/VISUAL SETUP Tom Foley ([email protected]); BobLura DOOR PRIZE Barbara Johnson ([email protected]) HOSPITALITY Mary McKenzie ([email protected]); Martha Wolfe SPECIAL HOSPITALITY Betsy Burdette ([email protected]) RAFFLE TICKETS Greeter/Membership table volunteers - Luli Westra, Dolly Dalton, Eleanor Kinzie, etc. RAFFLE COMMENTARY Larry Giroux GREETERS/ATTENDENCE Betty Ann Prevatt, Dolly Dalton([email protected]), Luli Westra SHOW & TELL Dale Kammerlohr FM-LEE GARDEN COUNCIL Mary McKenzie LIBRARIAN Sue Gordon ASSISTANT LIBRARIAN Kay Janssen The opinions expressed in the Meristem are those of the authors. They do not necessarily represent the views of the Editor or the official policy of CBS. -
Bromeliaceae
Bromeliaceae VOLUME XLI - No. 5 - SEPT/OCT 2007 The Bromeliad Society of Queensland Inc. P. O. Box 565, Fortitude Valley Queensland, Australia 4006, Home Page www.bromsqueensland.com OFFICERS PRESIDENT Olive Trevor (07) 3351 1203 VICE PRESIDENT Barry Kable PAST PRESIDENT Bob Reilly (07) 3870 8029 SECRETARY Chris Coulthard TREASURER Glenn Bernoth (07) 4661 3 634 BROMELIACEAE EDITOR Ross Stenhouse SHOW ORGANISER Bob Cross COMMITTEE David Rees, Paul Dunstan, Ann McBur - nie, Arnold James,Viv Duncan MEMBERSHIP SECRETARY Roy Pugh (07) 3263 5057 SEED BANK CO-ORDINATOR Doug Parkinson (07) 5497 5220 AUDITOR Anna Harris Accounting Services SALES AREA STEWARD Pat Barlow FIELD DAY CO-ORDINATOR Nancy Kickbusch LIBRARIAN Evelyn Rees ASSISTANT SHOW ORGANISER Phil Beard SUPPER STEWARDS Nev Ryan, Barry Genn PLANT SALES Nancy Kickbusch (Convenor) N. Poole (Steward) COMPETITION STEWARDS Dorothy Cutcliffe, Alan Phythian CHIEF COMPETITION STEWARD Jenny Cakurs HOSTESS Gwen Parkinson BSQ WEBMASTER Ross Stenhouse LIFE MEMBERS Grace Goode OAM Peter Paroz, Michael O’Dea Editors Email Address: [email protected] The Bromeliad Society of Queensland Inc. gives permission to all Bromeliad Societies to re- print articles in their journals provided proper acknowledgement is given to the original author and the Bromeliaceae, and no contrary direction is published in Bromeliaceae. This permission does not apply to any other person or organisation without the prior permission of the author. Opinions expressed in this publication are those of the individual contributor and may not neces- sarily reflect the opinions of the Bromeliad Society of Queensland or of the Editor Authors are responsible for the accuracy of the information in their articles.