How to Collect Fern Spores!
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1 5 Chapter 1 Introduction I. LIFE CYCLES and DIVERSITY of VASCULAR PLANTS the Subjects of This Thesis Are the Pteri
Chapter 1-15 Chapter 1 Introduction I. LIFE CYCLES AND DIVERSITY OF VASCULAR PLANTS The subjects of this thesis are the pteridophytes and seed plants that are conventionally classified as the vascular plants or tracheophytes. Vascular plants were traditionally defined by the possession of specialized conducting tissues, called phloem and xylem. Mosses are now believed to have inherited their conducting tissues from a common ancestor with the tracheophytes (Mishler & Churchill 1984) but are not considered in this thesis. Vascular plants can be divided into four groups with respect to life cycle. These groups are homosporous pteridophytes, heterosporous pteridophytes, gymnosperms and angiosperms. This is not intended to be a phylogenetic classification. There are about a quarter of a million species of vascular plant alive today. The vast majority are angiosperms and most of the remainder are homosporous pteridophytes. Heterosporous pteridophytes and gymnosperms contribute only a small number of species (Table 1.1). TABLE 1.1 Estimated number of extant species in each of the major groups of vascular plants (data from Parker 1982). Homosporous pteridophytes 12,000 species Heterosporous pteridophytes <1,000 species Gymnosperms <1,000 species Angiosperms >200,000 species A. Homosporous pteridophytes Homosporous pteridophytes produce a single type of spore. Spores are dispersed and develop into photosynthetic or mycoparasitic gametophytes. A gametophyte's gender is indeterminate at the time of spore dispersal, and a single gametophyte may produce eggs and/or sperm. Sperm are motile, and require free water to fertilize eggs. The young sporophyte is nourished by the maternal gametophyte during early development but later becomes Chapter 1-16 nutritionally independent. -
Reproduction in Plants Which But, She Has Never Seen the Seeds We Shall Learn in This Chapter
Reproduction in 12 Plants o produce its kind is a reproduction, new plants are obtained characteristic of all living from seeds. Torganisms. You have already learnt this in Class VI. The production of new individuals from their parents is known as reproduction. But, how do Paheli thought that new plants reproduce? There are different plants always grow from seeds. modes of reproduction in plants which But, she has never seen the seeds we shall learn in this chapter. of sugarcane, potato and rose. She wants to know how these plants 12.1 MODES OF REPRODUCTION reproduce. In Class VI you learnt about different parts of a flowering plant. Try to list the various parts of a plant and write the Asexual reproduction functions of each. Most plants have In asexual reproduction new plants are roots, stems and leaves. These are called obtained without production of seeds. the vegetative parts of a plant. After a certain period of growth, most plants Vegetative propagation bear flowers. You may have seen the It is a type of asexual reproduction in mango trees flowering in spring. It is which new plants are produced from these flowers that give rise to juicy roots, stems, leaves and buds. Since mango fruit we enjoy in summer. We eat reproduction is through the vegetative the fruits and usually discard the seeds. parts of the plant, it is known as Seeds germinate and form new plants. vegetative propagation. So, what is the function of flowers in plants? Flowers perform the function of Activity 12.1 reproduction in plants. Flowers are the Cut a branch of rose or champa with a reproductive parts. -
Bruxner Park Flora Reserve Working Plan
Bruxner Park Flora Reserve Working Plan Working Plan for Bruxner Park Flora Reserve No 3 Upper North East Forest Agreement Region North East Region Contents Page 1. DETAILS OF THE RESERVE 2 1.1 Introduction 2 1.2 Location 2 1.3 Key Attributes of the Reserve 2 1.4 General Description 2 1.5 History 6 1.6 Current Usage 8 2. SYSTEM OF MANAGEMENT 9 2.1 Objectives of Management 9 2.2 Management Strategies 9 2.3 Management Responsibility 11 2.4 Monitoring, Reporting and Review 11 3. LIST OF APPENDICES 11 Appendix 1 Map 1 Locality Appendix 1 Map 2 Cadastral Boundaries, Forest Types and Streams Appendix 1 Map 3 Vegetation Growth Stages Appendix 1 Map 4 Existing Occupation Permits and Recreation Facilities Appendix 2 Flora Species known to occur in the Reserve Appendix 3 Fauna records within the Reserve Y:\Tourism and Partnerships\Recreation Areas\Orara East SF\Bruxner Flora Reserve\FlRWP_Bruxner.docx 1 Bruxner Park Flora Reserve Working Plan 1. Details of the Reserve 1.1 Introduction This plan has been prepared as a supplementary plan under the Nature Conservation Strategy of the Upper North East Ecologically Sustainable Forest Management (ESFM) Plan. It is prepared in accordance with the terms of section 25A (5) of the Forestry Act 1916 with the objective to provide for the future management of that part of Orara East State Forest No 536 set aside as Bruxner Park Flora Reserve No 3. The plan was approved by the Minister for Forests on 16.5.2011 and will be reviewed in 2021. -
Heterospory: the Most Iterative Key Innovation in the Evolutionary History of the Plant Kingdom
Biol. Rej\ (1994). 69, l>p. 345-417 345 Printeii in GrenI Britain HETEROSPORY: THE MOST ITERATIVE KEY INNOVATION IN THE EVOLUTIONARY HISTORY OF THE PLANT KINGDOM BY RICHARD M. BATEMAN' AND WILLIAM A. DiMlCHELE' ' Departments of Earth and Plant Sciences, Oxford University, Parks Road, Oxford OXi 3P/?, U.K. {Present addresses: Royal Botanic Garden Edinburiih, Inverleith Rojv, Edinburgh, EIIT, SLR ; Department of Geology, Royal Museum of Scotland, Chambers Street, Edinburgh EHi ijfF) '" Department of Paleohiology, National Museum of Natural History, Smithsonian Institution, Washington, DC^zo^bo, U.S.A. CONTENTS I. Introduction: the nature of hf^terospon' ......... 345 U. Generalized life history of a homosporous polysporangiophyle: the basis for evolutionary excursions into hetcrospory ............ 348 III, Detection of hcterospory in fossils. .......... 352 (1) The need to extrapolate from sporophyte to gametophyte ..... 352 (2) Spatial criteria and the physiological control of heterospory ..... 351; IV. Iterative evolution of heterospory ........... ^dj V. Inter-cladc comparison of levels of heterospory 374 (1) Zosterophyllopsida 374 (2) Lycopsida 374 (3) Sphenopsida . 377 (4) PtiTopsida 378 (5) f^rogymnospermopsida ............ 380 (6) Gymnospermopsida (including Angiospermales) . 384 (7) Summary: patterns of character acquisition ....... 386 VI. Physiological control of hetcrosporic phenomena ........ 390 VII. How the sporophyte progressively gained control over the gametophyte: a 'just-so' story 391 (1) Introduction: evolutionary antagonism between sporophyte and gametophyte 391 (2) Homosporous systems ............ 394 (3) Heterosporous systems ............ 39(1 (4) Total sporophytic control: seed habit 401 VIII. Summary .... ... 404 IX. .•Acknowledgements 407 X. References 407 I. I.NIRODUCTION: THE NATURE OF HETEROSPORY 'Heterospory' sensu lato has long been one of the most popular re\ie\v topics in organismal botany. -
Dock and Crop Images
orders: [email protected] (un)subscribe: [email protected] Current Availability for September 25, 2021 Dock and Crop images Click any thumbnail below for the slideshow of what we shipped this past week: CYCS ARE RED HOT GIANT GLOSSY LEAVES BLUE MOONSCAPE SUCCULENT BLUE LEAVES SUCCULENT ORANGE LEAVES SPECKLED LEAVES CYCS ARE RED HOT RED SUNSETSCAPE Jeff's updates - 9/16 dedicated this week's favorites Chimi's favorite climbing structure 4FL = 4" pot, 15 per flat 10H = 10" hanging basket n = new to the list ys = young stock 6FL = 6" pot, 6 per flat 10DP = 10" Deco Pot, round b&b = bud and bloom few = grab 'em! QT= quart pot, 12 or 16 per flat nb = no bloom * = nice ** = very nice Quarts - 12 per flat, Four Inch - 15 per flat, no split flats, all prices NET code size name comments comments 19406 4FL Acalypha wilkesiana 'Bronze Pink' ** Copper Plant-colorful lvs 12210 QT Acorus gramineus 'Ogon' ** lvs striped creamy yellow 19069 4FL Actiniopteris australis ** Eyelash Fern, Ray Fern 17748 4FL Adiantum hispidulum ** Rosy Maidenhair 17002 4FL Adiantum raddianum 'Microphyllum' ** extremely tiny leaflets 21496 4FL Adromischus filicaulis (cristatus?) ** Crinkle Leaf 16514 4FL Aeonium 'Kiwi' ** tricolor leaves 13632 QT Ajuga 'Catlin's Giant' ** huge lvs, purple fls 13279 QT Ajuga pyramidalis 'Metallica Crispa' ** crinkled leaf 17560 4FL Aloe vera * Healing Aloe, a must-have 13232 QT Anthericum sanderii 'Variegated' *b&b grassy perennial 13227 QT Asparagus densiflorus 'Meyer's' ** Foxtail Fern 19161 4FL Asplenium 'Austral Gem' -
Growth of Fern Gametophytes After 20 Years of Storage in Liquid Nitrogen
FERN GAZ. 20(8): 337-346. 2018 337 GROWTH OF FERN GAMETOPHYTES AFTER 20 YEARS OF STORAGE IN LIQUID NITROGEN V. C. Pence Center for Conservation and Research of Endangered Wildlife (CREW) Cincinnati Zoo & Botanical Garden, 3400 Vine Street, Cincinnati, OH 45220, USA email: [email protected] Key words: cryopreservation, ex situ conservation, gametophyte; in vitro; long-term storage ABSTRACT In vitro grown gametophytes of six species of ferns, which had been cryopreserved using the encapsulation dehydration procedure, were evaluated for survival after 20 yrs of storage in liquid nitrogen. Tissues were rewarmed and transferred to a recovery medium with the same methods originally used to test pre-storage viability. All six species resumed growth. Post-storage viability was not consistently higher or lower than pre-storage viability of LN exposed tissues, likely reflecting the small sample sizes. However, these results demonstrate that long-term storage in liquid nitrogen is a viable option for preserving gametophytes of at least some fern species and could be utilized as an additional tool for preserving valuable gametophyte collections and for the ex situ conservation of fern biodiversity. INTRODUCTION For many species of ferns, gametophyte tissues have proven to be highly adaptable to growth in vitro (Table 1) . Most of these have been initiated through the aseptic germination of spores, although the aseptic germination of gemmae has also been demonstrated (Raine & Sheffield, 1997). As in vitro cultures, gametophytes can provide tissues for research and for propagation, both for ornamental ferns as well as for ferns of conservation concern. The ex situ conservation of ferns has traditionally relied on living collections and spore banks (Ballesteros, 2011). -
Palaeogeograph Y, Palaeoclimatology, Palaeoecology , 17(1975): 157--172 © Elsevier Scientific Publishing Company, Amsterdam -- Printed in the Netherlands
Palaeogeograph y, Palaeoclimatology, Palaeoecology , 17(1975): 157--172 © Elsevier Scientific Publishing Company, Amsterdam -- Printed in The Netherlands CLIMATIC CHANGES IN EASTERN ASIA AS INDICATED BY FOSSIL FLORAS. II. LATE CRETACEOUS AND DANIAN V. A. KRASSILOV Institute of Biology and Pedology, Far-Eastern Scientific Centre, U.S.S.R. Academy of Sciences, Vladivostok (U.S.S.R.) (Received June 17, 1974; accepted for publication November 11, 1974) ABSTRACT Krassilov, V. A., 1975. Climatic changes in Eastern Asia as indicated by fossil floras. II. Late Cretaceous and Danian. Palaeogeogr., Palaeoclimatol., Palaeoecol., 17:157--172. Four Late Cretaceous phytoclimatic zones -- subtropical, warm--temperate, temperate and boreal -- are recognized in the Northern Hemisphere. Warm--temperate vegetation terminates at North Sakhalin and Vancouver Island. Floras of various phytoclimatic zones display parallel evolution in response to climatic changes, i.e., a temperature rise up to the Campanian interrupted by minor Coniacian cooling, and subsequent deterioration of cli- mate culminating in the Late Danian. Cooling episodes were accompanied by expansions of dicotyledons with platanoid leaves, whereas the entire-margined leaf proportion increased during climatic optima. The floristic succession was also influenced by tectonic events, such as orogenic and volcanic activity which commenced in Late Cenomanian--Turonian times. Major replacements of ecological dominants occurred at the Maastrichtian/Danian and Early/Late Danian boundaries. INTRODUCTION The principal approaches to the climatic interpretation of fossil floras have been outlined in my preceding paper (Krassilov, 1973a). So far as Late Creta- ceous floras are concerned, extrapolation (i.e. inferences from tolerance ranges of allied modern taxa) is gaining in importance and the entire/non-entire leaf type ratio is no less expressive than it is in Tertiary floras. -
Hybrids in the Fern Genus Osmunda (Osmundaceae)
Bull. Natl. Mus. Nat. Sci., Ser. B, 35(2), pp. 63–69, June 22, 2009 Hybrids in the Fern Genus Osmunda (Osmundaceae) Masahiro Kato Department of Botany, National Museum of Nature and Science, Amakubo 4–1–1, Tsukuba, 305–0005 Japan E-mail address: [email protected] Abstract Four described putative hybrids in genus Osmunda, O. intermedia from Japan, O. rug- gii from eastern U.S.A., O. nipponica from central Japan, and O. mildei from southern China, are enumerated with notes on their hybridity. It is suggested that Osmunda intermedia is an intrasub- generic hybrid (O. japonica of subgenus Osmunda ϫ O. lancea of subgenus Osmunda), O. ruggii is an intersubgeneric hybrid (O. regalis of subgenus Osmunda ϫ O. claytoniana of subgenus Clay- tosmunda), O. nipponica is an intersubgeneric hybrid (O. japonica ϫ O. claytoniana of subgenus Claytosmunda), and O. midlei is an intersubgeneric hybrid (O. japonica ϫ O. angustifolia or O. vachellii of subgenus Plenasium). Among the four, O. intermedia is the most widely distributed and can reproduce in culture, suggesting that it can reproduce to some extent in nature. Key words : Hybrid, Osmunda intermedia, Osmunda mildei, Osmunda nipponica, Osmunda rug- gii. three subgenera Claytosmunda, Osmunda, and Introduction Plenasium, genus Leptopteris, genus Todea, and The genus Osmunda has been classified in ei- genus Osmundastrum (see also Metzgar et al., ther the broad or narrow sense. In the previously 2008). most accepted and the most lumping classifica- Four putative hybrids are known in the genus tion, it was divided into three subgenera, Osmun- Osmunda s.l. in eastern U.S.A. -
Atoll Research Bulletin No. 503 the Vascular Plants Of
ATOLL RESEARCH BULLETIN NO. 503 THE VASCULAR PLANTS OF MAJURO ATOLL, REPUBLIC OF THE MARSHALL ISLANDS BY NANCY VANDER VELDE ISSUED BY NATIONAL MUSEUM OF NATURAL HISTORY SMITHSONIAN INSTITUTION WASHINGTON, D.C., U.S.A. AUGUST 2003 Uliga Figure 1. Majuro Atoll THE VASCULAR PLANTS OF MAJURO ATOLL, REPUBLIC OF THE MARSHALL ISLANDS ABSTRACT Majuro Atoll has been a center of activity for the Marshall Islands since 1944 and is now the major population center and port of entry for the country. Previous to the accompanying study, no thorough documentation has been made of the vascular plants of Majuro Atoll. There were only reports that were either part of much larger discussions on the entire Micronesian region or the Marshall Islands as a whole, and were of a very limited scope. Previous reports by Fosberg, Sachet & Oliver (1979, 1982, 1987) presented only 115 vascular plants on Majuro Atoll. In this study, 563 vascular plants have been recorded on Majuro. INTRODUCTION The accompanying report presents a complete flora of Majuro Atoll, which has never been done before. It includes a listing of all species, notation as to origin (i.e. indigenous, aboriginal introduction, recent introduction), as well as the original range of each. The major synonyms are also listed. For almost all, English common names are presented. Marshallese names are given, where these were found, and spelled according to the current spelling system, aside from limitations in diacritic markings. A brief notation of location is given for many of the species. The entire list of 563 plants is provided to give the people a means of gaining a better understanding of the nature of the plants of Majuro Atoll. -
Spore Reproduction of Japanese Climbing Fern in Florida As a Function of Management Timing
Spore Reproduction of Japanese Climbing Fern in Florida as a Function of Management Timing Candice M. Prince1, Dr. Gregory E. MacDonald1, Dr. Kimberly Bohn2, Ashlynn Smith1, and Dr. Mack Thetford1 1University of Florida, 2Pennsylvania State University Photo Credit: Chris Evans, University of Illinois, Bugwood.org Exotic climbing ferns in Florida Old world climbing fern Japanese climbing fern (Lygodium microphyllum) (Lygodium japonicum) Keith Bradley, Atlas of Florida Vascular Plants Chris Evans, University of Illinois, Bugwood.org Japanese climbing fern (Lygodium japonicum) • Native to temperate and tropical Asia • Climbing habit • Early 1900s: introduced as an ornamental1 • Long-distance dispersal via wind, pine straw bales2,3 Chris Evans, University of Illinois, Bugwood.org Dennis Teague, U.S. Air Force, Bugwood.org Distribution • Established in 9 southeastern states • In FL: present throughout the state, USDA NRCS National Plant Data Team, 2016 but most invasive in northern areas • Winter dieback, re-sprouts from rhizomes1 • Occurs in mesic and temporally hydric areas1 Atlas of Florida Vascular Plants, Institute of Systemic Botany, 2016 Impacts Chris Evans, University of Illinois, Bugwood.org • Smothers and displaces vegetation, fire ladders • Florida Exotic Pest Plant Council: Category I species Chuck Bargeron, University of Georgia, Bugwood.org • Florida Noxious Weed List • Alabama Noxious Weed List (Class B) Japanese climbing fern: life cycle John Tiftickjian, Sigel Lab, University of Delta State University Louisiana at Lafayette -
Plant Anatomy Lab 5
Plant Anatomy Lab 7 - Stems II This exercise continues the previous lab in studying primary growth in the stem. We will be looking at stems from a number of different plant species, and emphasize (1) the variety of stem tissue patterns, (2) stele types and the location of vascular tissues, (3) the development of the stem from meristem activity, and (4) the production of xylem and phloem by the procambium. All of the species studied are pictured either in your text or the atlases at the front of the lab. 1) Early vascular plants (cryptogams) A) Obtain a piece of the rachis of the fern (collected in the White Hall atrium). This structure is superficially analogous to a stem, although it has a different origin. Prepare a transverse section of the rachis and stain it in toluidine blue. Note the large amount of cortical tissue and the presence of sclerenchyma cells near the outer cortex. Also note that the stele vascular tissue appears to be amphiphloic. Lastly, you should be able to see readily the endodermal-style thickenings on the cells just outside each vascular bundle. B) Find prepared slides of the Osmunda and Polypodium (fern) rhizomes. Note the amphiphloic bundles (a protostele?), the presence of sclerenchyma in the cortex, and the thickened walls of the endodermis that you will find is not uncommon among many non-seed plants. Remember that rhizomes are modified stems that often occur underground. Osmunda fern vascular bundle. C) Obtain a prepared slide of Psilotum. This stele does not have a pith, so it is a protostele (or an actinostele because it has a star-like shape). -
Educator Guide
Educator Guide Presented by The Field Museum Education Department INSIDE: s )NTRODUCTION TO "OTANY s 0LANT $IVISIONS AND 2ELATED 2ESEARCH s #URRICULUM #ONNECTIONS s &OCUSED &IELD 4RIP !CTIVITIES s +EY 4ERMS Introduction to Botany Botany is the scientific study of plants and fungi. Botanists (plant scientists) in The Field Museum’s Science and Education Department are interested in learning why there are so many different plants and fungi in the world, how this diversity is distributed across the globe, how best to classify it, and what important roles these organisms play in the environment and in human cultures. The Field Museum acquired its first botanical collections from the World’s Columbian Exposition of 1893 when Charles F. Millspaugh, a physician and avid botanist, began soliciting donations of exhibited collections for the Museum. In 1894, the Museum’s herbarium was established with Millspaugh as the Museum’s first Curator of Botany. He helped to expand the herbarium to 50,000 specimens by 1898, and his early work set the stage for the Museum’s long history of botanical exploration. Today, over 70 major botanical expeditions have established The Field’s herbarium as one of the world’s preeminent repositories of plants and fungi with more than 2.7 million specimens. These collections are used to study biodiversity, evolution, conservation, and ecology, and also serves as a depository for important specimens and material used for drug screening. While flowering plants have been a major focus during much of the department’s history, more recently several staff have distinguished themselves in the areas of economic botany, evolutionary biology and mycology.