The Genera Cattleyopsis Lem., Laeliopsis Lindl. and Broughtonia R. Br. Reestablished

Similar documents
Cover Page. The handle holds various files of this Leiden University dissertation.

Speciation Plant Sciences, 2001Updated: June 1, 2012 Gale Document Number: GALE CV

EPICLADIUM SMALL OR GUARIANTHE DRESSLER & W.E. HIGGINS (ORCHIDACEAE)? JOHN BECKNER

Materials and Methods

ROGH Docent Program Week 4: Orchid Biology.

Prosthechea madrensis, a reconsideration of Epidendrum madrense Schltr. (Orchidaceae: Laeliinae)

5/31/17. Week 10; Monday MEMORIAL DAY NO CLASS. Page 88

THE ECOLOGY AND CULTIVATION OF TERRESTRIAL ORCHIDS OF ARGENTINA

Common Name: FLORIDA ADDER S-MOUTH ORCHID. Scientific Name: Malaxis spicata Swartz. Other Commonly Used Names: none

Cyclamen libanoticum, a species that knows its identity!

EVOLUTION Unit 1 Part 9 (Chapter 24) Activity #13

SPECIATION. REPRODUCTIVE BARRIERS PREZYGOTIC: Barriers that prevent fertilization. Habitat isolation Populations can t get together

The practice of naming and classifying organisms is called taxonomy.

A naturally occurring hybrid between Asclepias syriaca L. and A. purpurascens L. (Apocynaceae, Asclepiadoideae) Richard E. Rintz

CONSIDERATION OF PROPOSALS FOR AMENDMENT OF APPENDICES I AND II

Chapter 24-Flowering Plant and Animal Coevolution

Unit 10.4: Macroevolution and the Origin of Species

Biology, Quarter 4, Unit 4.1. Evolution. Overview

The Origin of Species

BIOLOGY 366 PLANT SYSTEMATICS FINAL EXAM 100 POINTS

The pollination of European orchids Part 7: Autogamy: Neotinea maculata and Corallorhiza trifida by Jean Claessens and Jacques Kleynen

Apomixis in Plants. Authors. Sven E. Asker, Ph.D. Department of Genetics University of Lund Lund, Sweden

CLASS XI BIOLOGY NOTES CHAPTER 1: LIVING WORLD

BIOLOGY 317 Spring First Hourly Exam 4/20/12

LENTIBULARIACEAE BLADDERWORT FAMILY

TAXONOMY. GENERAL INFORMATION Alaska, Canada, Northeast United States, Greenland

Historical Biogeography. Historical Biogeography. Historical Biogeography. Historical Biogeography

Common Name: GLADE MEADOW-PARSNIP. Scientific Name: Thaspium pinnatifidum (Buckley) Gray. Other Commonly Used Names: cutleaf meadow-parsnip

Taxonomy. Content. How to determine & classify a species. Phylogeny and evolution

ON SOLIDAGO MACVAUGHII (ASTERACEAE: ASTEREAE), A RARE MEXICAN ENDEMIC OF THE TORTIFOLIAE GROUP OF SOLIDAGO. SUBSECT. TRIPLINERVIAE

FIELD IDENTIFICATION CARDS FOR INVASIVE NON-NATIVE PLANT SPECIES KNOWN TO THREATEN ARIZONA WILDLANDS.

# Mo. Bot. Garden. ORCHID REVIEW THE VOLUME I WEST, NEWMAN, & CO. ^n gruitst%*citefc litcmtljhj gouvnal DEVOTED TO ORCHIDOLOGY IN ALL ITS BRANCHES

Pilea nummulariifolia (creeping Charlie)

The Origin of Species

Objectives. ROGH Docent Program Week 2: Plant Anatomy

Pollination by Fungus Gnats in Mitella formosana (Saxifragaceae)

Chapter 17A. Table of Contents. Section 1 Categories of Biological Classification. Section 2 How Biologists Classify Organisms

Aegopodium podagraria (Goutweed Bishop's weed )

ORCHIDOLOGY ORH CREDITS. Orchid Hunting is a mortal occupation. - Susan Orlean, The Orchid Thief WEB ONLINE INSTRUCTOR:

Comparison of flowering plant diversity and insect diversity at varying elevations across Dominica, West Indies. By Brent Goebel

Green Culture Singapore Feature Article for June Published on 15 July Text by Lim Xuan Hong

Area of Focus: Biology. Learning Objective 1: Describe the structure and function of organs. Pre-Learning Evaluation: Teaching Methods and Process:

Leucothrinax morrisii, a New Name for a Familiar Caribbean Palm

Lab sect. (TA/time): Botany 113 Spring First Hourly Exam 4/21/00

A RANGE EXTENSION FOR CYPRIPEDIUM MON- TANUM DOUGLAS EX LINDLEY (ORCHIDACEAE) INTO THE BLACK HILLS OF SOUTH DAKOTA

Need for systematics. Applications of systematics. Linnaeus plus Darwin. Approaches in systematics. Principles of cladistics

Figure 1. Consider this cladogram. Let s examine it with all three species concepts:

THE THEORY OF EVOLUTION

OCR (A) Biology A-level

SBEL 1532 HORTICULTURE AND NURSERY Lecture 2: Plants Classification & Taxonomy. Dr.Hamidah Ahmad

Plant Systematics. What is Systematics? or Why Study Systematics? Botany 400. What is Systematics or Why Study Systematics?

Germplasm. Introduction to Plant Breeding. Germplasm 2/12/2013. Master Gardener Training. Start with a seed

Introduction to Plant Breeding. Master Gardener Training

Population Genetics & Evolution

Biology 1B Evolution Lecture 9 (March 15, 2010), Speciation Processes

Lab sect. (TA/time): Biology 317 Spring Third Hourly (Final) Exam 6/8/10

Name Date Class. Patterns of Evolution

Anatomy of Flowering Plants

CHAPTER-1 THE LIVING WORLD MULTIPLE CHOICE QUESTIONS

Heredity and Evolution

PLANT VARIATION AND EVOLUTION

Ch. 4- Plants. STRUCTURE AND FUNCTION And Taxonomy

Speciation. Today s OUTLINE: Mechanisms of Speciation. Mechanisms of Speciation. Geographic Models of speciation. (1) Mechanisms of Speciation

THE THEORY OF EVOLUTION

Harvard Papers in Botany

LANKESTERIANA 18(2): BOOKS

BIOS 5970: Plant-Herbivore Interactions Dr. Stephen Malcolm, Department of Biological Sciences

Georgia Performance Standards for Urban Watch Restoration Field Trips

Stomata Density of Orchids and Cloud Forest Humidity

Chapter 22: Descent with Modification 1. BRIEFLY summarize the main points that Darwin made in The Origin of Species.

Common Name: SHOALS SPIDER-LILY. Scientific Name: Hymenocallis coronaria (J. LeConte) Kunth. Other Commonly Used Names: Cahaba lily, Catawba lily

06/09/05. A survey of the plant kingdom based on a detailed study of the morphology, anatomy and physiology of selected representative specimens.

Changing Planet: Changing Mosquito Genes

A handful of primary features are useful for distinguishing water primrose (Ludwigia) from other plants. Understand what to look for, such as leaf

The Evolutionary Biology Of Plants By Karl J. Niklas READ ONLINE

Print Names and Classification

Class 10 Heredity and Evolution Gist of lesson

Heredity and Evolution

Darw r i w n n a nd n t h t e e G ala l pa p gos Biolo l gy g L c e t c u t re r e 16 1 : 6 Ma M cr c o r ev e olu l ti t on

HEREDITY AND EVOLUTION

Northwestern Garter Snake (Thamnophis. ordinoides)

CURRENT CONCEPTS IN PLANT TAXONOMY

Objectives. To identify plant structures and functions. To describe the structure of plant cells. To explain the process of reproduction in plants.

Christel Anne Ross. Invasion Success by Plant Breeding

Evolution - Unifying Theme of Biology Microevolution Chapters 13 &14

P t a ter e ns n s o f o E v E o v l o u l t u io i n

Thursday, March 21, 13. Evolution

Creating an e-flora for South Africa

Speciation. Today s OUTLINE: Mechanisms of Speciation. Mechanisms of Speciation. Geographic Models of speciation. (1) Mechanisms of Speciation

The Living World. AIIMS,CBSE,AIPMT, AFMC,Bio.Tech & PMT, Contact : , Mail at :- by AKB

regions such as Greenland, northern Europe

Chapter 16: Reconstructing and Using Phylogenies

Evolution Common Assessment 1

A SECOND RECESSIVE FACTOR FOR BROWN PERICARP IN MAIZE.*

FIRST REPORT OF CEROPEGIA BULBOSA ROXB. FROM COASTAL HABITAT OF KULABA FORT, ALIBAG, MAHARASHTRA

3 Domains of Living Things Bacteria and Archaea are prokaryotic organisms.

Speciation. Today s OUTLINE: Mechanisms of Speciation. Mechanisms of Speciation. Geographic Models of speciation. (1) Mechanisms of Speciation

EVOLUTION change in populations over time

2. What is meiosis? The process of forming gametes (sperm and egg) 4. Where does meiosis take place? Ovaries- eggs and testicles- sperm

Plant Names and Classification

Transcription:

ISSN 2325-4785 New World Orchidaceae Nomenclatural Notes Nomenclatural Note Issue No. 23 July 8, 2016 www.newworldorchidaceae.com The Genera Cattleyopsis Lem., Laeliopsis Lindl. and Broughtonia R. Br. Reestablished Ruben P. Sauleda 22585 SW 187 Ave. Miami, Fl. 33170 ABSTRACT The genera Cattleyopsis Lem. and Laeliopsis Lindl. are reestablished. The characters that clearly separate the genera including the cdna data are given. The expansion or redefinition of the genus Broughtonia R. Br. to include the characters of Cattleyopsis and Laeliopsis is rejected. There have been several differences of opinion considering the three genera Broughtonia R. Br., Cattleyopsis Lem. and Laeliopsis Lindl. Three taxonomic approaches to the classification of these genera have been proposed. Several authors have considered the three genera as distinct (Correll, 1941; Leon, 1946; Dietrich, 1984; Sauleda & Adams, 1984; Withner, 1996), others have considered only two genera incorporating Laeliopsis into Broughtonia and only recognizing Broughtonia and Cattleyopsis (Rofle, 1889; Cogniaux, 1910; Schlechter, 1915; Acuña, 1939; Fowlie, 1961a and 1961b). The third approach recognizes only the genus Broughtonia lumping Laeliopsis and Cattleyopsis into Broughtonia (Fawcett & Rendle, 1910; Dressler, 1966; Loigier, 1969; Adams, 1970 and 1971; Diaz Dumas, 1996; Nir, 2000; Diaz Dumas, 2014; Mújica et al., 2015; Mújica & González, 2015). Dressler (1966) united the species of Cattleyopsis with Broughtonia because of the very close floral resemblances between Broughtonia sanguinea (Sw.) R. Br. and Cattleyopsis ortgiesiana (Rchb. f.) Cogn. and between Broughtonia domingensis (Lindl.) Rolfe and Cattleyopsis lindenii (Lindl.) Cogn., as well as the vegetative resemblances between B. domingensis and C. lindenii. Dressler states that the only distinction between Broughtonia and Cattleyopsis is the number of pollinia; Cattleyopsis has eight pollinia and Broughtonia have four 1

pollinia and those that consider the number of pollinia to be an inviolable generic feature will, of course, maintain Cattleyopsis as a distinct genus. He adds that the distinction drawn by Lindley (1853) between Broughtonia and Laeliopsis was based on a morphological misconception (the external adnate spur of Broughtonia), that has been quite untenable when the plants of extreme western Jamaica are considered (Broughtonia negrilensis Fowlie). In addition, Dressler confused Epidendrum cubense Lindl. (Cattleyopsis cubense (Lindl.) Sauleda & Adams) with Barkeria chinensis (Lindl.) L. B. Thien. He stated that after examining the type specimen of E. cubense he agreed with the conclusion previously reached by him and L. B. Thien that it is B. chinensis and added that he doubted the Cuban origin of the plant (E. cubense). Sauleda & Adams (1984) published a comprehensive and detailed monograph of the three genera. They addressed most of Dressler s misconceptions and added several important features of the three genera, which were unknown to Dressler. Each genus is restricted to a separate island. Laeliopsis occurs only in Hispanola, Broughtonia only occurs in Jamaica and Cattleyopsis is restricted to Cuba and the Bahama Islands. The Bahamian occurrence is not unusual since most if not all of the species in the Bahama Islands also occur in Cuba and apparently migrated from Cuba to the Bahama Islands. The geographic isolation of the genera is a character that cannot be ignored. The distinctive distributional patterns suggest evolutionary divergence as a function of isolation (Dobzhansky, 1940). Dressler also gave the floral similarity as a reason for uniting B. sanguinea and C. ortgiesiana and giving the same reason for uniting B. domingensis and C. lindenii. This similarity is due to convergent evolution on a pollination system. Broughtonia sanguinea and C ortgiesiana have been observed being visited by hummingbirds and B. domingensis and C. lindenii have been observed being visited by bees. The floral differences of the species within the genera Broughtonia and Cattleyopsis are due to the adaptive nature of floral traits due to pollinator- mediated microevolution (Harder & Johnson, 2009). Shifts in pollination systems result in correlated shifts in floral traits and speciation within a genus (Forest et al., 2014; Van der Niet et al., 2014). Lindley (1853) gave the distinction between Broughtonia and Laeliopsis as an external adnate spur. Dressler says this is a morphological misconception, and has proven to be quite untenable when the plants of extreme western Jamaica are considered in reference to B. negrilensis. Sauleda & Adams (1984) have demonstrated in clear drawings of cross-sectional dissections of living flowers that the plants of western Jamaica (B. negrilensis) do have this structure and what 2

Lindley considered an external adnate spur is actually a well-defined swollen nectary embedded within the ovary. In Cattleyopsis and Laeliopsis the nectary lumen is wide at its distal opening gradually narrowing proximally, this is not so in Broughtonia where the proximal end of the nectary lumen swells to a nectarfilled chamber. This externally visible proximal swelling has been confused with a spur or sepaline tube. Arditti (1969) and Arditti and Fisch (1977) were the only researchers to recognize the true nature of the prominent proximal nectary chamber present only in Broughtonia. The presence of the nectary and the results of pigment analyses led Arditti and Fisch (1977) to question the lumping of Cattleyopsis and Laeliopsis into Broughtonia. The number of pollinia is an important character, especially when taken in consideration with the other important characters. This did not seem important to Dressler at the time. It is clearly evident that Cattleyopsis and Laeliopsis, which occur on different islands from Broughtonia, evolved this character independently from Broughtonia. Cattleyopsis and Laeliopsis are more closely related to each other than to Broughtonia. Diaz Dumas (1996) states that Broughtonia is a natural group and a separation into multiple genera cannot be done and therefore follows the opinion of Dressler. Diaz Dumas recognizes the geographical isolation of each genus as Sauleda & Adams (1984) demonstrated but ignores all the other characters that clearly separate the three genera. Many authors currently follow Diaz Dumas s treatment reducing Cattleyopsis and Laeliopsis to Broughtonia based on Dressler s treatment (Nir, 2000; Valle et al., 2010; Acevedo-Rodríguez & Strong, 2012; Mújica & González, 2015; Mújica et al., 2015). The characters that separate the three genera must be revisited. The reproductive isolation of the three genera makes them endemic to their respective islands. The floral similarities among members of each genus are attributable to secondary adaptations to ornithophily or to melittophily (Sauleda & Adams, 1984). This is a good example of convergent evolution. The vegetative similarities of the four species that comprise Cattleyopsis and Laeliopsis are attributable to secondary adaptation to the xeric habitats in which they occur (Sauleda & Adams, 1984; Lowry et al., 2014). Laeliopsis makes vegetative phenotypic adjustments to environmental conditions. Vegetatively Laeliopsis resembles Broughtonia in mesic habitats and Cattleyopsis in xeric habitats (Sauleda & Adams, 1984). In Cattleyopsis and Laeliopsis the nectary lumen is wide at its distal opening gradually narrowing proximally, this is not so in Broughtonia where the proximal end of the nectary lumen swells to a nectar-filled chamber. This externally visible proximal swelling has been confused with a spur or sepaline tube. 3

Broughtonia sanguinea (Sw.) R. Br. Column and ovary, lateral view and serial cross-sections showing swollen nectary lumen. From Sauleda & Adams (1984). Broughtonia negrilensis Fowlie. Column and ovary, lateral view and serial cross-sections showing swollen nectary lumen. From Sauleda & Adams (1984). The columns of the three genera are distinctively different. The column of Cattleyopsis has two auricle-like appendages near the base and is narrowly winged towards the apex. Broughtonia have a short blunt column with thick and short wings near the apex. In Laeliopsis the column is elongate, clavate and narrowly winged towards apex. 4

Cattleyopsis cubensis (Lindl.) Sauleda & Adams. Column and ovary, lateral view and serial cross-sections showing nectary lumen. From Sauleda & Adams (1984). Cattleyopsis ortgiesiana (Rchb. f.) Cogn. Column and ovary, lateral view and serial cross-sections showing nectary lumen. From Sauleda & Adams (1984). 5

Cattleyopsis lindenii (Lindl.) Cogn. Column and ovary, lateral view and serial cross-sections showing nectary lumen. From Sauleda & Adams (1984). Laeliopsis domingensis (Lindl.) Lindl. Column and ovary, lateral view and serial cross-sections showing nectary lumen. From Sauleda & Adams (1984). 6

Comparison of live material of Cattleyopsis lindenii (Top) and Broughtonia sanguinea (Bottom) demonstrating the diagnostic characters of each. Several authors continue to include the species of Cattleyopsis and Laeliopsis in Broughtonia based in part on the results of plastid DNA sequences (van den Berg et al., 2009). However, the same cdna results (van den Berg et al., 2009) can be used to conclude that only two species belong in Broughtonia and that the species of Laeliopsis and Cattleyopsis are distinct. 7

cdna results from van den Berg et al., 2009, indicating that Broughtonia negrilensis and Broughtonia sanguinea belong in the same genus and that Cattleyopsis and Laeliopsis are separate genera. There is a disturbing trend to modify and expand the concept or definition of a genus to accommodate the plastid DNA results (Sauleda, 2016). The lumping of the genera Sophronitis Lindl. and Laelia Lindl. into the genus Cattleya Lindl. (van den Berg, 2008) and the lumping of the species that belong in the genera Anacheilium Hoffmanns, Pollardia Withner & Harding, Euchile Withner and Panarica Withner & Harding into Prosthechea Knowles & Westc. (Higgins, 1997) based solely on molecular analysis and totally ignoring the morphology are prime examples of expanding the generic descriptions. By including the species of Cattleyopsis and Laeliopsis in Broughtonia the concept of the genus has to be greatly expanded from the original description. The characters used to expand the generic concept of Broughtonia include changes in geographical distribution, structure of the column and vegetative characters. To the description of the column as a short blunt column as originally described in Broughtonia now must be added a narrow slender column as found in Laeliopsis and with basal auricle-like appendages as found in Cattleyopsis. The number of pollinia, the presence of eight must now be added to the original description of four. To the vegetative description of Broughtonia of a broad coriaceous leaf with entire margin and ellipsoid to ovoid pseudobulbs now must be added narrow fleshy-rigid leaves with erose margin and cylindrical pseudobulbs. Diaz Dumas (2014) made these additions to the concept of Broughtonia in the treatment of Broughtonia in Orchid flora of the Greater Antilles. Considering the extensive changes that have to be made to the generic concept of Broughtonia as described by Robert Brown, Diaz Dumas treatment of the genus Broughtonia although not illegal under the International Code of Nomenclature is an affront and demonstrates a lack of respect for the work of Robert Brown and other previous authors. 8

According to article 47A.1. of the International Code of Nomenclature when an alteration.. has been considerable, the nature of the change may be indicated by adding.. abbreviated where suitable, emendavit (emend.) followed by the name of the author responsible for the change. Broughtonia as revised by Diaz Dumas differs from the genus as originally circumscribed by Robert Brown, but the generic name remains Broughtonia R. Br. since the type of the name is still included in the genus but should be cited as Broughtonia R. Br. emend. Diaz Dumas. The distributional data, morphological data, results of pigment analyses and cdna data are extensive enough to substantiate that Broughtonia, Cattleyopsis and Laeliopsis should be maintained as separate genera as Sauleda and Adams (1984) suggested. The concept of the genus Broughtonia should not be modified to include characters of two other genera. This photograph is from William Osment s personal collection of photographs taken in Cuba. It represents the first plant of Cattleyopsis cubensis he brought to the United States in the 1950 s. 9

These are pictures of the result of the self-pollination of a plant of Cattleyopsis cubensis collected by William Osment in Prov. de Pinar del Rio, Cuba in July 1959. The original plant was self-compatible as are the resulting seedlings. 10

Results of self-pollinating a seedling of Cattleyopsis cubensis from the original plant collected by William Osment (F2). This photograph is from William Osment s personal collection of photographs taken in Cuba. It represents the first plant of Cattleyopsis ortgiesiana he brought to the United States in the 1950 s. 11

ACKNOWLEDGMENT I am indebted to Pablo Esperon for the photographs of the F2 seedling and the comparison of the live material. I also wish to give the late Carl L. Withner credit for the pioneering work that he did with this group and the inspiration that he was early in my career. LITERATURE CITED Acevedo-Rodríguez, P. and Mark T. Strong. 2012. Catalogue of Seed Plants of the West Indies. Smithsonian Contributions to Botany, no. 98, xxv + 1192 pages. Acuña Gale, J. 1939. Catalogo Descriptibo de las Orquideas Cubanas. Boletin no. 60: pp. 1-221. Estacion Experimental Agronomica, Santiago de las Vegas, Cuba. Adams. C. D. 1970. Broughtonia A Brief Review. The Florida Orchidist 13: pp. 8-11. Adams, C. D. 1971. Broughtonia Again. The Florida Orchidist 14: pp. 101-105. Arditti, J. 1969. Floral Anthocyanins in Species and Hybrids of Broughtonia, Brassavola and Cattleyopsis (Orchidaceae). Amer. J. Bot. 56: pp. 59-68. Arditti, J. and M. H. Fisch. 1977. Anthocyanins of the Orchidaceae: Distribution, Heredity, Functions Synthesis and Localization. In: Orchid Biology. Reviews and Perspectives 1. ed. J. Arditti. Cornell University Press. Ithaca, New York. Cogniaux, A. 1910. In: Urban, I., Symbolae Antillanae (Orchidaceae). 6: pp. 293-696. Reprinted 1964. A. Asher & Co., Amsterdam. Correll, D. S. 1941. Notes concerning Some West Indian Orchids 1. The Genus Broughtonia and Some if its Allies. Bot. Mus. Leaflets. Harvard Univ. 10: pp. 41-58. Diaz Dumas, M. A. 1996. Revision de los Generos Antillanos Broughtonia R. Brown, Cattleyopsis Lemaire y Laeliopsis Lindley (Orchidaceae). Revista del Jardin Botanico Nacional. Vol. 17/18: pp. 9-16. Díaz Dumas, M. A. 2014. Broughtonia, pp. 52-56. In: Ackerman, J. D. and Collaborators, Orchid flora of the Greater Antilles. Memoirs of The New York Botanical Garden. Vol. 109. 12

Dietrich, H. 1984. Orchidaceae Cubanae novae II: Die Orchidee 35: pp. 200-202. Dobzhansky, Th. 1940. Speciation as a Stage in Evolutionary Divergence The American Naturalist. Vol. 74, No. 753: pp. 312-321. Dressler, R. L. 1966. Nomenclatural Notes on the Orchidaceae III. Taxon. Vol. 15 (6): pp. 241-243. Fawcett. W. and A. B. Rendle. 1919. Flora of Jamaica. Vol. 1 Orchidaceae. London, England. Forest, F., P. Goldblatt, J. C., Manning, D. Baker, J. F. Colville, D. S. Devey, S. Jose, M. Kaye and S. Buerki. 2014. Pollinator Shifts as Triggers of Speciation in Painted Petal Irises (Lapeirousia: Iridaceae). Annals of Botany 113: pp. 357 371. Fowlie, J. A. 1961a. Ecological Notes: Natural Hybridization in the Genus Broughtonia. Amer. Orchid Soc. Bull. 30: pp. 707-710. Fowlie, J. A. 1961b. Obscure Species. The Orchid Digest 25: pp. 416-418. Harder, L. D., S. D. Johnson. 2009. Darwin s Beautiful Contrivances: Evolutionary and Functional Evidence for Floral Adaptation. New Phytologist 183: pp. 530-545. Higgins, W. 1997. A Reconsideration of the Genus Prosthechea. Phytologia, Vol. 82 (5). Leon, Her. 1946. Flora de Cuba. Contribuciones Ocasionales del Museo de Historia Natural del Colegio de la Salle. No. 8. Orquideas: pp. 341-404. Habana, Cuba. Lindley, J. 1853. Paxton s Flower Garden. Vol. III. Bradbury and Evans. London. Liogier, A. H. 1969. Flora de Cuba. Suplemento. Editorial Sucre. Caracas. Venezuela. 13

Lowry, David B., Kyle Hernandez, Samuel H. Taylor, Eli Meyer, Tierney L. Logan, Kerrie W. Barry, Jarrod A. Chapman, Daniel S. Rokhsar, Jeremy Schmutz, Thomas E. Juenger. 2014. The Genetics of Divergence and Reproductive Isolation Between Ecotypes of Panicum hallii. New Phytologist. Vol. 205 (1): pp. 402-414. Mújica, Ernesto, Elaine González, José L. Bocourt, Esther L. SantaCruz and J. M. Díaz. 2015. A New Natural Hybrid of Broughtonia (Orchidaceae) From Cuba. Lankesteriana 15(3): pp. 183-185. Mújica, Ernesto and Elaine González. 2015. A New Checklist of Orchid Species from Cuba. Lankesteriana. Vol. 15(3): pp. 219-269. Nir, MA. 2000. Orchidaceae Antillanae. DAG Media Publishing, Inc. USA. Rolfe, R. A. 1889. List of Garden Orchids. Gard. Chor. Ser. 3, 5: pp. 491. Sauleda, R. P. 2016. A Locality for Maxillaria aureoglobula Christenson in Colombia. New World Orchidaceae Nomenclatural Notes. Nomenclatural Note Issue No. 21. Epublished. Sauleda, R. P. & R. M. Adams. 1984. A Reappraisal of the Orchid Genera Broughtonia R. Brown, Cattleyopsis Lemaire and Laeliopsis Lindley. Rhodora 86, 848: pp. 445-467. Schlechter, R. 1915. Die Orchideen. Paul Parey, Berlin. Vale, A., D. Rojas, J. C. Alvarez and L. Navarro. 2010. Breeding System and Factors Limiting Fruit Production in the Nectarless Orchid Broughtonia lindenii. Plant Biology 13 (Suppl. 1), pp. 51 61. German Botanical Society and The Royal Botanical Society of the Netherlands. Van den Berg, Cassio. 2008. New Combinations in the Genus Cattleya Lindl. (Orchidaceae). Neodiversity: A Journal of Neotropical Biodiversity 3-12. Van den Berg,, Cássio, Wesley E. Higgins, Robert L. Dressler, Mark Whitten, Miguel A. Soto-Arenas and Mark W. Chase. 2009. A Phylogenetic Study of Laeliinae (Orchidaceae) Based on Combined Nuclear and Plastid DNA Sequences. Ann. Bot. 104(3): pp. 417-430. 14

Van der Niet, T., Rod Peakall and Steven D. Johnson. 2014. Pollinator-driven Ecological Speciation in Plants: New Evidence and Future Perspectives. Ann. of Bot. Vol. 113 (2): pp. 199-212. Withner, Carl L. 1996. The Cattleyas and Their Relatives. Vol. IV. The Bahamain and Caribbean Species. Timber Press, Inc. Portland, Oregon. 15