September 2017

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September 2017 September 2017 President: Mike Kandt 838-6681, [email protected] Vice-President: Wanita Wright, 733-6626, [email protected] Treasurer: Larry Determann 945-0017, [email protected] Secretary: Susan Kandt, 838-6681, [email protected] Newsletter Editor: Mike Kandt 838-6681, [email protected] Webmaster: Wayne Determann, [email protected] FROM THE PRESIDENT September Meeting By Mike Kandt Saturday, September 2 6:00 PM - ? It almost happened again. A rain-out. But thanks to our hosts, Gale Lane At and family, when the rain hit at about the start of our meeting, we were able to scurry inside a large garage building to eat and hear Gail’s presentation Well Garden and demo on building a deer chaser fountain. Sorry about the mix-up Industries beforehand. I didn’t know Gail had such a great backup plan. Thanks to 1440 W. Douglas, Wichita Gail and family for their gracious hospitality. (About 4 blocks west of Seneca Susan, Wanita and I have returned from the 2017 International Waterlily on Douglas in Delano) and Watergarden Symposium in Pennsylvania where we were inundated over four days. We visited Longwood Gardens, Chanticleer Gardens, Aquaponics Winterthur, Mount Cuba, several private gardens, and garden centers. And this didn’t count the evening informal discussions with some of the world’s Aquaponics is the science that uses leading experts in watergardens and plants. One whole day was devoted to waste from raising fish to fertilize seminars on all kinds of topics. I’m still trying to process all the info we plants and vegetables. Well Garden picked up, but you will hear more in months to come. Industries is developing Aquaponics setups from small aquariums to large In September, we will learn about Aquaponics at a local business called commercial installations. Well Garden Industries located in Delano. Well Garden is developing Aquaponics setups from small aquariums to large commercial installations. We’ll have our normally fantastic Aquaponics is the science that uses waste from raising fish to fertilize potluck buffet. Please bring a main plants and vegetables. This is an even more technically advanced version dish and a side or dessert and lawn of the installation we saw in Wamego a few years ago. We will tour their chairs. Paper plates and plastic forks facility and check out lots of ways to grow fish and plants in limited space. are provided, but you are also welcome to bring your own plates and Also in September, we will caravan to the Oklahoma City water garden service. Drinks will be provided. tour on Saturday, September 9. It’s not too late to get your reservation in, so call or contact Wanita Wright ASAP. See the box later in this newsletter. In October we meet at Hong’s Nursery and have a presentation on bee- UPCOMING EVENTS keeping. Yes, bees are important pollinators of water plants, too. Sept 2: KPS Meeting Sept 9: Road trip - OKC Pond In November we will have our auction. NOTE THAT THE DATE HAS Tour CHANGED to the 11th to coordinate with Botanica’s room reservations. Oct 7: KPS Meeting We will have some large pieces of pond liner available at the auction that Nov 11: KPS Auction has been donated by ABC Roofing. So start collecting your donation items Dec 2: KPS Holiday Party and saving your cash for this event. WELCOME NEW MEMBERS Stay cool!!! Jane Byrnes Deb Wierenga SWAP SHOP ADVERTISING RATES If you have articles, plants or fish to sell or give away, let me know at 838- Business Card Size Ad (about 2" x 3 ½"): 6681 or [email protected] $15 per 3-month period; $50 per year Want Small KOI – [email protected] Quarter-Page Ad (about 3 ½" x 4 ½"): $30 per 3-month period; $100 per year Two new green plastic rain barrels; $30.00 each. Carol Half-Page Ad (about 5" x 7 ½"): $60 per 3- Daney, [email protected] month period; $200 per year Full-Page Ad (8 ½” x 11"): $400 per year UV light for sale - 10,000 gal. capacity plus 2 replacement bulbs. Unused, $300. New price of $950 and replacement bulbs at $127. Carol Daney, [email protected] FREE KOI BABIES Did you know… that need to find good homes. We are cleaning my pond the last Saturday of Well water has very low oxygen levels and may be high in carbon dioxide (CO2). The September. If you would like some, please best way to fill your pond with well water is to aerate it by spraying into the pond. CALL Wanita, 733-6626 wcw Water Lilies at Longwood Gardens WATER PLANTS (by Mike Kandt) Victoria Water Lily Nymphaeaceae Victoria amazonica I know I have written about this wonderful plant before, but we just returned from Longwood Gardens in Pennsylvania where several were on display, and you just can't help getting excited about this amazing water lily. Victoria Amazonica The Victoria water lily is also called the Water Platter. Leaves can get to be larger than 6 feet in diameter. Edges are turned up, prompting the term "Platter". All surfaces of the leaves below water and the stems are covered with lethal spines. Because of the size and spines, not too many grow this plant at home. It is usually reserved for large botanical garden displays. The large leaves can support up to 150 pounds. You will see many photos of babies and children sitting on the floating leaves. There are two types of native Victoria: victoria amazonica and victoria cruziana. The former thrives in the waterways of the Amazon river. The latter comes from Argentina and Paraguay and has a taller rim. In 1960, Patrick Nutt from Longwood Gardens successfully crossed the amazonica and the cruziana to create the Longwood hybrid. This is the plant that grows at Botanica in Wichita. The Victoria is a tropical lily and will not survive frost. It must be Victoria Cruziana grown from seed every year. If you do want to try at home, starts are available from a limited number of southern growers. A single plantlet sprout can cost almost $100, and these are difficult to grow to maturity. Victorias have large fragrant flowers that smell like pineapple. The blooms open at night, close the next morning, and last three days. They then form seeds if pollinated. If you choose to grow a Victoria, plan for a lot of space. A single plant can cover 15 feet in diameter. Pots for these plants are recommended to be up to 60” by 18” deep and need warm water, lots of sun, and fertilizer to grow. Some have tried to dwarf these by growing in smaller pots. One goal of modern hybridizers is to create a consistent dwarf Victoria that can be marketed for smaller ponds. This would be nice for backyard ponders, but I bet this will take a while. There are many books written specially about this one plant that has fascinated the botanical world for centuries. Check one out or at least Google “Victoria Water Lilies” and learn more. Victoria Longwood hybrid, back of leaf BIO-FILTERS By Mike Kandt Good water quality doesn't just happen. It requires a little planning and some maintenance. Decaying debris from leaves, fish waste and other organic stuff that finds its way into your pond can add nutrients to the water as it decomposes. Ammonia, also from fish waste, also adds nitrogen to the water that is toxic to fish and will cause algae blooms. The more fish there are and the larger the fish, the worse the problem is. The solution is a bio-filter properly sized and maintained. A plant bog can be a bio-filter, but for this discussion, I will address fabricated bio-filters. Many think that those little foam pads in their skimmer are their pond bio-filter. Nope! They only function to keep the pump in the skimmer from clogging. If you have a larger bio-filter, you can actually remove these foam pads and not have to clean them daily. The finer debris should go through the pump and get caught in the bio-filter. Some ponds have a container at the head of the pond, sometimes called a “bio- falls”. While this may do some bio-filtration if it has media, it is usually too small and usually less than 30 gallons. So what is a bio-filter and how does it work? A bio-filter not only filters solids from the water, it uses bacteria growing on filter media to consume the ammonia and convert it to non-toxic nitrites that plants will use. It will remove suspended solids and dissolved ammonia. It helps to add some oxygen by splashing the water coming into the filter or by adding an air line and bubbler. This keeps the good bacteria (aerobic) alive. The bad anaerobic bacteria will stink. This is the stuff that grows in a septic tank. Good aeration will help prevent this. The bio-filter media can be anything that will not corrode and has a lot of surface area. I started using gravel and lava rock, but it worked so well that it packed up quickly with pond muck and was impossible to clean. I then switched to plastic media of various types. I tried "bio-balls" specifically made for this. Worked, but too expensive. I now use plastic shavings. Plastic scrubber brushes work well. I've even heard of someone using recycled plastic spoons. Crumpled plastic window screen can work in a pinch. Put the media in net bags (laundry bags from Walmart), fill with media, and put in the filter container, trying to seal any open water paths.
Recommended publications
  • A Study of the Floral Biology of Viciaria Amazonica (Poepp.) Sowerby (Nymphaeaceae)
    A study of the Floral Biology of Viciaria amazonica (Poepp.) Sowerby (Nymphaeaceae) Ghillean T. Prance (1) Jorge R. Arias (2) Abstract Victoria and the beetles which visit the flowers in large numbers, and to collect data A field study of the floral biology of Victoria on V. amazonica to compare with the data of amazonica (Poepp.) Sowerby (Nymphaeaceae) was Valia & Girino (1972) on V. cruziana. made for comparison with the many studies made in cultivated plants, of Victoria in the past. In thE: study areas in the vicinity of Manaus, four species HISTORY OF WORK ON THE FLORAL of Dynastid beetles were found in flowers of V. BIOLOGY OF VICTORIA. amazonica, three of the genus Cyclocephala and one o! Ligyrus . The commonest species of beetle The nomenclatura( and taxonomic history proved to be a new species of Cyclocephala and was found in over 90 percent of the flowers studied. of the genus has already been summarized in The flowers of V. amazonica attract beetles by Prance (1974). where it has been shown that their odour and their white colour on the first the correct name for the Amazonian species day that they open. The beetles are trapped in the of Victoria is V. amazonica, and not the more flower for twenty-four hours and feed on the starchy carpellary appendages. Observations were frequently used name, V. regia. The taxonomic made of flower temperature, which is elevated up history is not treated further here. to 11 aC above ambient temperature, when the flower Victoria amazonica has been a subject of emits the odour to attract the beetles.
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  • 2279 Knapp-Checklisttag.Indd
    A peer-reviewed open-access journal PhytoKeys 9: 15–179Checklist (2012) of vascular plants of the Department of Ñeembucú, Paraguay 15 doi: 10.3897/phytokeys.9.2279 CHECKLIST www.phytokeys.com Launched to accelerate biodiversity research Checklist of vascular plants of the Department of Ñeembucú, Paraguay Juana De Egea1,2, Maria Peña-Chocarro1, Cristina Espada1, Sandra Knapp1 1 Department of Botany, Th e Natural History Museum, Cromwell Road, London SW7 5BD, United Kingdom 2 Wildlife Conservation Society Paraguay, Capitán Benitez Vera 610, Asunción, Paraguay Corresponding author: S. Knapp ([email protected]) Academic editor: Susanne Renner | Received 25 October 2011 | Accepted 6 January 2012 | Published 30 January 2012 Citation: De Egea J, Peña-Chocarro M, Espada C, Knapp S (2012) Checklist of vascular plants of the Department of Ñeembucú, Paraguay. PhytoKeys 9: 15–179. doi: 10.3897/phytokeys.9.2279 Abstract Th e Department of Ñeembucú is one of the least well-documented areas of eastern Paraguay, and the fl ora is composed of a mixture of forest and Chaco elements. Regions like Ñeembucú are often considered of lower diversity and interest that more forested regions; this results from both actual species richness fi gures and from under-collecting due to perception as uninteresting. We present here a checklist of the vascular plants of Ñeembucú, which includes 676 taxa (including infraspecifi c taxa and collections identifi ed only to genus) in 100 families and 374 genera. Four hundred and thirty nine (439) of these are new records for Ñeembucú and of these, 4 are new published records for Paraguay.
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  • Pollen Ontogeny in Victoria (Nymphaeales)
    Int. J. Plant Sci. 174(9):1259–1276. 2013. ᭧ 2013 by The University of Chicago. All rights reserved. 1058-5893/2013/17409-0006$15.00 DOI: 10.1086/673246 POLLEN ONTOGENY IN VICTORIA (NYMPHAEALES) Mackenzie L. Taylor,1,* Patrick J. Hudson,2,† Jolene M. Rigg,† Julie N. Strandquist,† Julie Schwartz Green,3,† Tara C. Thiemann,4,† and Jeffrey M. Osborn‡ *Department of Biology, Creighton University, Omaha, Nebraska 68178, USA; †Department of Biology, Truman State University, Kirksville, Missouri 63501, USA; and ‡School of Science, College of New Jersey, Ewing, New Jersey 08628, USA Editor: William E. Friedman Premise of research. Water lilies (Nymphaeales) make up one of the oldest independent lineages of an- giosperms. The giant water lily, Victoria, exhibits pollination and floral traits that are derived within Nym- phaeales. Specialization in pollination and floral biology is often reflected in pollen traits, and in Victoria,this is evidenced by the production of permanent tetrads. Compound pollen has evolved many times across the angiosperm phylogeny, but compound pollen development has been investigated in only a few taxa, and the degree of developmental variation in microspore cohesion is unknown. This article comprehensively charac- terizes the pollen ontogenetic sequence in Victoria for the first time. Methodology. Floral buds of Victoria amazonica, Victoria cruziana, and Longwood hybrid were field collected. Anthers at the sporogenous, microspore mother cell, tetrad, “free” microspore, and mature pollen grain stages were studied using combined LM/SEM/TEM. Pivotal results. Microspore cohesion in Victoria differs from that exhibited by the few compound pollen- producing taxa that have been studied. In Victoria, the calymmate tetrads fuse via crosswall cohesion, but cytoplasmic connections are transient and do not serve as a template for wall bridge formation.
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  • PART 2 AUTHOR INDEX of ARTICLES in the I.W.G.S. LIBRARY C = Copy Sheets
    5 PART 2 AUTHOR INDEX OF ARTICLES IN THE I.W.G.S. LIBRARY c = copy sheets Abbott, Charles C. 1888. NYMPHAEA TUBEROSA IN EASTERN WATERS. Garden & Forest (issue unknown) c1 Ames, Oakes. 1900. AN INTERESTING GROUP OF NEW HYBRID BLOOMING NYMPHAEAS. American Gardening 21:644 c1 Anderson, Edgar. 1965. VICTORIA WATER LILIES. Mo. Bot. Gard. Bull. 53(5): 1-18 c11 Anderson, Fred. WATER LILIES FOR COOL SUMMER BEAUTY. Horticulture. August 1960: c2 Anderson, Michael G. & S.W. Idso. 1987. SURFACE GEOMETRY AND STOMATAL CONDUCTANCE EFFECTS ON EVAPORATION FROM AQUATIC MACROPHYTES. Water Resources Research. 23(6):1037-1042 c6 Andre {Editor of Revue Horticole}.1896. NEW HARDY WATER LILIES .The Garden 50:325 c1 Anthony, John. AN ILLUSTRATED LIFE OF SIR JOSEPH PAXTON. Shire Lifelines Book No. 21 c25 Armstrong, Wayne P. 1983a. A MARRIAGE BETWEEN A FERN AND AN ALGA. Environmental Southwest. Winter 1983: 20-24 c5 -----1983b THE WORLD'S SMALLEST WILDFLOWER. Environment Southwest, Summer 1983: 17-21 c5 Aston, Helen I. 1973. NYMPHOIDES OF AUSTRALIA. c13 -----1982 . NEW AUSTRALIAN SPECIES OF NYMPHOIDES. Muelleria 5:35-51 c17 -----1984. NYMPHOIDES TRIANGULARIS AND N. ELLIPTICA; TWO NEW AUSTRALIAN SPECIES. Muelleria 5265-270 c6 -----1985a. MONOCHORIA CYANEA AND M. AUSTRALASICA IN AUSTRALIA. Muelleria 651-57 c7. -----1985b. NYMPHOIDES OF PAPUA NEW GUINEA. Freshwater plants of PNG: 180-185 c6 -----1986. NYMPHOIDES DISPERMA. Muelleria 6(3):197-200 c4 -----1987a. LYMNOPHYTON AUSTRALIENSE A NEW GENERIC RECORD FOR AUSTRALIA. Muelleria 6(5):311-316 c6 -----1987b. NYMPHOIDES BELEGENSIS. Mulleria 6(5): 359-362 c4 -----1997. NYMPHOIDES SPINULOSPERMA: A NEW SPECIES FROM S.E.
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  • Thermogenesis in Three Philodendron Species (Araceae) of French Guiana Marc Gibernau1 and Denis Barabé2
    Thermogenesis in three Philodendron species (Araceae) of French Guiana Marc Gibernau1 and Denis Barabé2 1. Laboratoire d’Ecologie Terrestre, Université Paul Sabatier, 118 Route de Narbonne, Bat 4R3, 31062 Toulosue cedex 4, France. E-mail: [email protected] 2. Institut de Recherche en Biologie Végétale, Université de Montréal, Jardin Botanique de Montréal, 4101 rue Sherbrooke Est, Montréal (Québec), Canada H1X 2B2. Abstract Spadix temperature was measured in three species of Philodendron: P. acutatum, P. pedatum and P. solimoesense. These species showed two different patterns of spadix temperature during their flowering cycle. In P. acutatum and P. pedatum (subgenus Philodendron), the spadix warmed up twice during the beginning of each flowering night with a temperature not significantly different from that of ambient air between the two peaks. In P. solimoesense (subgenus Meconostigma), the spadix temperature rose up to 14oC above that of ambient air during the first night, then it progressively cooled down but remained 3-6oC above ambient air temperature. We propose that the heat production and the spadix temperature patterns observed may reflect different physiological processes and have a taxonomic significance in the genus Philodendron. Keywords: Araceae, flowering cycle, flower temperature, heating flower. Résumé Nous avons mesuré la température du spadice chez trois espèces de Philodendron: P. acutatum, P. pedatum et P. solimoesense. Deux types de courbe de température des spadices ont été observés. Les spadices de P. acutatum, P. pedatum (sous-genre Philodendron) produisent deux pics distincts de chaleur lors des deux soirs de la floraison. Entre ces pics de chaleur, la température du spadice n’est pas différente de celle de l’air ambient.
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  • Annual Report 2009
    XISHUANGBANNA TROPICAL BOTANICAL GARDEN, CHINESE ACADEMY OF SCIENCES Headquarter Kunming Division Menglun, Mengla 88 Xuefu Road, Kunming Yunnan 666303, P. R. China Yunnan 650223, P. R. China Tel. + 86 691 8715460 Tel. + 86 871 5171169 Fax. + 86 691 8715070 Fax. + 86 871 5160916 www.xtbg.cas.cn Annual Report 2009 Captions for cover photos (anti-clockwise ) 1. Physiognomy of Bulong Nature Reserve; 2. Celebration of the 50th Anniversary; 3. Exhibition in Wuhan Botanical Garden; 4. Wild edible plants collection; 5. The 5th International Symposium on Zingiberaceae Xishuangbanna Tropical Botanical Garden 6. 2009 Graduation ceremony; 7. Experts’ visit to the construction site of the Chinese Academy of Sciences new research center Prepared by: FANG Chunyan HU Huabin Edited by: CHEN Jin Annual Report 2009 Xishuangbanna Tropical Botanical Garden Chinese Academy of Sciences March 31, 2010 Xishuangbanna Tropical Botanical Garden (XTBG), Chinese Academy of Sciences is a non-profit, comprehensive botanical garden involved in scientific research, plant diversity conservation and public science education, affiliated directly to the Chinese Academy of Sciences. XTBG’s vision: Financial Review Desirable base for plant diversity conservation and ecological studies. Noah’s Ark for tropical plants. XTBG’s mission: Promote science development and environmental conservation through implementing scientific research on ecology and plant diversity conservation, horticultural exhibition, and public education. 2 CONTENTS th XTBG 50 Anniversary .................................................................................
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  • An Example from the Floral Epidermis Ofthe Nymphaeaceae
    Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2018 Disentangling historical signal and pollinator selection on the micromorphology of flowers: an example from the floral epidermis ofthe Nymphaeaceae Coiro, Mario ; Barone Lumaga, Maria Rosaria Abstract: The family Nymphaeaceae includes most of the diversity among the ANA‐grade angiosperms. Among the species of this family, floral structures and pollination strategies are quite varied. The genus Victoria, as well as subgenera Lotos and Hydrocallis in Nymphaea, presents night‐blooming, scented flowers pollinated by scarab beetles. Such similar pollination strategies have led to macromorphological similarities among the flowers of these species, which could be interpreted as homologies or convergences based on different phylogenetic hypotheses about the relationships of these groups. We employed SEM of floral epidermis for seven species of the Nymphaeaceae with contrasting pollination biology to identify the main characters of the floral organs and the potential homologous nature of the structures involved in pollinator attraction. Moreover, we used TEM to observe ultrastructure of papillate‐conical epidermis in the stamen of Victoria cruziana. We then tested the phylogenetic or ecological distribution of these traits using both consensus network approaches and ancestral state reconstruction on fixed phylogenies. Our results show that the night‐blooming flowers present different specializations in their epidermis, with Victoria cruziana presenting the most elaborate floral anatomy. We also identify for the first timethe presence of conical‐papillate cells in the order Nymphaeales. The epidermal characters tend to reflect phylogenetic relationships more than convergence due to pollinator selection.
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  • Rhinoceros Beetles Pollinate Water Lilies in Africa (Coleoptera: Scarabaeidae: Dynastinae; Magnoliidae: Nymphaeaceae)
    SHORT COMMUNICATIONS ECOTROPICA 9: 103–106, 2003 © Society for Tropical Ecology RHINOCEROS BEETLES POLLINATE WATER LILIES IN AFRICA (COLEOPTERA: SCARABAEIDAE: DYNASTINAE; MAGNOLIIDAE: NYMPHAEACEAE) Frank-Thorsten Krell1, Gunnar Hirthe 2,Rüdiger Seine 3 & Stefan Porembski 2 1Department of Entomology, The Natural History Museum, Cromwell Road, London SW7 5BD, U.K.* 2 Institut für Biodiversitätsforschung, Allgemeine & Spezielle Botanik, Universität Rostock, Wismarsche Str. 8, D-18051 Rostock, Germany 3 European Astronaut Centre, Linder Höhe, D-51147 Köln, Germany Key words: Cantharophily, pollination, Afrotropics, Ruteloryctes morio, Cyclocephalini, Dynastinae, Nymphaea lotus, Nym- phaeaceae. In South America, night-blooming species of Nym- beetle species (Anomala sp., Scarabaeidae: Rutelinae) phaea L. water lilies and other Nymphaeaceae are pol- and bees (Apidae) in Nymphaea flowers. The records linated by scarab beetles of the subfamily Dynastinae of R. morio are listed below: (rhinoceros beetles) (Gottsberger 1986, Wiersema – Côte d’Ivoire, southern part of the PN Comoé, 1988). Nearly all of them belong to the endemic “pond Hyperolius”, 8°45’18”N, 3°46’37”W, 22. 09. American genera Cyclocephala Latreille, Erioscelis Bur- 1996, 22:00–23:00 h (Fig. 1), 3 to 5 individuals of meister, and Chalepides Casey (Valla & Cirino 1972, Ruteloryctes morio in each flower, altogether a few Gottsberger 1986, Schatz 1990) of the tribe Cyclo- dozen specimens (R.S.); 27. 09. 1999 and 01. 08.–15. cephalini. In South America a species of a different 09. 2000 (G.H.) (0/2 ❹ /1 ❹, 1 ➁ in coll. Hirthe; 1 dynastine tribe has been found in Victoria flowers on only two occasions, Ligyrus similis Endro“ di, 1968 (Prance & Arias 1975).
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  • Why the Monophyly of Nymphaeaceae Currently Remains Indeterminate: an Assessment Based on Gene-Wise Plastid Phylogenomics
    Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 3 May 2019 doi:10.20944/preprints201905.0002.v1 Article Why the monophyly of Nymphaeaceae currently remains indeterminate: An assessment based on gene-wise plastid phylogenomics Michael Gruenstaeudl 1,* 1 Institut für Biologie, Freie Universität Berlin, 14195 Berlin, Germany; [email protected] * Correspondence: [email protected] Received: date; Accepted: date; Published: date Abstract: The monophyly of Nymphaeaceae (water lilies) represents a critical question in understanding the evolutionary history of early-diverging angiosperms. A recent plastid phylogenomic investigation claimed new evidence for the monophyly of Nymphaeaceae, but its results could not be verified from the available data. Moreover, preliminary gene-wise analyses of the same dataset provided partial support for the paraphyly of the family. The present investigation aims to re-assess the previous conclusion of the monophyly of Nymphaeaceae under the same dataset and to determine the congruence of the phylogenetic signal across different plastome genes and data partition strategies. To that end, phylogenetic tree inference is conducted on each of 78 protein-coding plastome genes, both individually and upon concatenation, and under four data partitioning schemes. Moreover, the possible effects of various sequence variability and homoplasy metrics on the inference of specific phylogenetic relationships are tested using multiple logistic regression. Differences in the variability of polymorphic sites across codon positions are assessed using parametric and non-parametric analysis of variance. The results of the phylogenetic reconstructions indicate considerable incongruence among the different gene trees as well as the data partitioning schemes. The results of the multiple logistic regression tests indicate that the fraction of polymorphic sites of codon position 3 has a significant effect on the recovery of the monophyly of Nymphaeaceae.
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  • Comparative Serology of the Order Nymphaeales. II. Relationships of Nymphaeaceae and Nelumbonaceae Jean-Pierre Simon Rancho Santa Ana Botanic Garden
    Aliso: A Journal of Systematic and Evolutionary Botany Volume 7 | Issue 3 Article 5 1971 Comparative Serology of the Order Nymphaeales. II. Relationships of Nymphaeaceae and Nelumbonaceae Jean-Pierre Simon Rancho Santa Ana Botanic Garden Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons Recommended Citation Simon, Jean-Pierre (1971) "Comparative Serology of the Order Nymphaeales. II. Relationships of Nymphaeaceae and Nelumbonaceae," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 7: Iss. 3, Article 5. Available at: http://scholarship.claremont.edu/aliso/vol7/iss3/5 ALISO VoL. 7, No. 3, pp. 325-350 APRIL 22, 1971 COMPARATIVE SEROLOGY OF THE ORDER NYMPHAEALES II. RELATIONSHIPS OF NYMPHAEACEAE AND NELUMBONACEAE. JEAN-PIERRE SIMON Rancho Santa Ana Botanic Garden Claremont, California 91711 INTRODUCTION In a continuing effort to elucidate the serological reiationships of taxa of the aquatic order Nymphaeales, I am reporting here additiona,l data ob­ ta,ined from cross-reactions with antiser-a produced against species of Nu­ phar, Nymphaea, Victoria and Euryale. An earlier study established that Nelumbo wias serologically isolated from the remaining species of the Order ( Simon, 1970). In addition, the data showed that N elumbo had serological affinities with members of the Magnolia.Jes, Ranuncu1ales and Papaverales which were of the same magnitude to those found between N elumbo and the remaining taxa of the Nymphaeales. MATERIALS AND METHODS Extracts of representative species of Nymphaeales, Magnoliales, Ranun­ cu1ales and other orders of Angiosperms, as listed in Tables 2 and 3 of Simon ( 1970), were inves•tigated. Seeds of additional species of these and other orders of Angiosperms have since been available for this study ( Table 3 and text).
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  • University of Florida Thesis Or Dissertation Formatting
    IN VITRO PHYSIOLOGY OF RECALCITRANT TISSUE CULTURED PLANTS IN THE NYMPHAEACEAE, ALISMATACEAE, AND ORCHIDACEAE By HOANG NGUYEN A DISSERTATION PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY UNIVERSITY OF FLORIDA 2016 © 2016 Hoang H. Nguyen To Huong, Mom, Dad, Huy, Dale and Dr. Kane ACKNOWLEDGMENTS “I once dreamed that I could walk through the trees that are full of blooming ghost orchids” said Larry Richardson of the Florida Panther National Wildlife Refuge. Dear Larry, your dream is coming true. And so is mine. My dream, reflected through this study and this dissertation, could not be completed without the continuing support from friends, colleagues, and instructors. I deeply thank my major advisor, Dr. Michael Kane, who has guided me from the first days in the US. He is not only my teacher, my mentor, but he is also my cheerleader. Thank you for letting me do what I love, and giving me room to grow. I would like to thank my committee members, Drs. Charles Guy, Dennis Gray, Gregory Macdonald, and Hector Perez for their guidance. I especially appreciate Drs. Sandra Wilson, Hector Perez, Stuart McDaniel, and Thomas Colquhoun for allowing me to use their research equipment and spending their time to discuss my research with me. I thank Drs. Thomas Sheehan, Harold Koopowitz, Carlos Fighetti, and Mr. Frank Smith of American Orchid Society, who inspired me tremendously with their humility, knowledge, and true love of orchids. This study is proof of the strong collaboration between the University of Florida, the Florida Panther National Wildlife Refuge (Larry Richardson, Mark Danaher, Ben Nottingham, Kevin Godsea), and Illinois College (Dr.
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