Lesson 19. Reproduction in Plants
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Evolutionary Ecology of Pollination and Reproduction of Tropical Plants
TROPICAL BIOLOGY AND CONSERVATION MANAGEMENT - Vol. V - Evolutionary Ecology af Pollination and Reproduction of Tropical Plants - M. Quesada, F. Rosas, Y. Herrerias-Diego, R. Aguliar, J.A. Lobo and G. Sanchez-Montoya EVOLUTIONARY ECOLOGY OF POLLINATION AND REPRODUCTION OF TROPICAL PLANTS M. Quesada and F. Rosas Centro de Investigaciones en Ecosistemas, Universidad Nacional Autónoma de México, México. Y. Herrerias-Diego Universidad Michoacana de San Nicolás de Hidalgo, Michoacán, México. R. Aguilar IMBIV - UNC - CONICET, C.C. 495,(5000) Córdoba, Argentina J.A. Lobo Escuela de Biología, Universidad de Costa Rica G. Sanchez-Montoya Centro de Investigaciones en Ecosistemas, Universidad Nacional Autónoma de México, México. Keywords: Pollination, tropical plants, diversity, mating systems, gender, conservation. Contents 1. Introduction 1.1. The Life Cycle of Angiosperms 1.2. Overview of Angiosperm Diversity 2. Degree of specificity of pollination system 3. Diversity of pollination systems 3.1. Beetle Pollination (Cantharophily) 3.2. Lepidoptera 3.2.1. Butterfly Pollination (Psychophily) 3.2.2. Moth Pollination (Phalaenophily) 3.3. Hymenoptera 3.3.1. Bee PollinationUNESCO (Melittophily) – EOLSS 3.3.2. Wasps 3.4. Fly Pollination (Myophily and Sapromyophily) 3.5. Bird Pollination (Ornitophily) 3.6. Bat PollinationSAMPLE (Chiropterophily) CHAPTERS 3.7. Pollination by No-Flying Mammals 3.8. Wind Pollination (Anemophily) 3.9. Water Pollination (Hydrophily) 4. Reproductive systems of angiosperms 4.1. Strategies that Reduce Selfing and/or Promote Cross-Pollination. 4.2. Self Incompatibility Systems 4.2.1. Incidence of Self Incompatibility in Tropical Forest 4.3. The Evolution of Separated Sexes from Hermaphroditism 4.3.1. From Distyly to Dioecy ©Encyclopedia Of. Life Support Systems (EOLSS) TROPICAL BIOLOGY AND CONSERVATION MANAGEMENT - Vol. -
Evolutionary Trajectories Explain the Diversified Evolution of Isogamy And
Evolutionary trajectories explain the diversified evolution of isogamy and anisogamy in marine green algae Tatsuya Togashia,b,c,1, John L. Barteltc,d, Jin Yoshimuraa,e,f, Kei-ichi Tainakae, and Paul Alan Coxc aMarine Biosystems Research Center, Chiba University, Kamogawa 299-5502, Japan; bPrecursory Research for Embryonic Science and Technology, Japan Science and Technology Agency, Kawaguchi 332-0012, Japan; cInstitute for Ethnomedicine, Jackson Hole, WY 83001; dEvolutionary Programming, San Clemente, CA 92673; eDepartment of Systems Engineering, Shizuoka University, Hamamatsu 432-8561, Japan; and fDepartment of Environmental and Forest Biology, State University of New York College of Environmental Science and Forestry, Syracuse, NY 13210 Edited by Geoff A. Parker, University of Liverpool, Liverpool, United Kingdom, and accepted by the Editorial Board July 12, 2012 (received for review March 1, 2012) The evolution of anisogamy (the production of gametes of dif- (11) suggested that the “gamete size model” (Parker, Baker, and ferent size) is the first step in the establishment of sexual dimorphism, Smith’s model) is the most applicable to fungi (11). However, and it is a fundamental phenomenon underlying sexual selection. none of these models successfully account for the evolution of It is believed that anisogamy originated from isogamy (production all known forms of isogamy and anisogamy in extant marine of gametes of equal size), which is considered by most theorists to green algae (12). be the ancestral condition. Although nearly all plant and animal Marine green algae are characterized by a variety of mating species are anisogamous, extant species of marine green algae systems linked to their habitats (Fig. -
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. -
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE LILIACEAE de Jussieu 1789 (Lily Family) (also see AGAVACEAE, ALLIACEAE, ALSTROEMERIACEAE, AMARYLLIDACEAE, ASPARAGACEAE, COLCHICACEAE, HEMEROCALLIDACEAE, HOSTACEAE, HYACINTHACEAE, HYPOXIDACEAE, MELANTHIACEAE, NARTHECIACEAE, RUSCACEAE, SMILACACEAE, THEMIDACEAE, TOFIELDIACEAE) As here interpreted narrowly, the Liliaceae constitutes about 11 genera and 550 species, of the Northern Hemisphere. There has been much recent investigation and re-interpretation of evidence regarding the upper-level taxonomy of the Liliales, with strong suggestions that the broad Liliaceae recognized by Cronquist (1981) is artificial and polyphyletic. Cronquist (1993) himself concurs, at least to a degree: "we still await a comprehensive reorganization of the lilies into several families more comparable to other recognized families of angiosperms." Dahlgren & Clifford (1982) and Dahlgren, Clifford, & Yeo (1985) synthesized an early phase in the modern revolution of monocot taxonomy. Since then, additional research, especially molecular (Duvall et al. 1993, Chase et al. 1993, Bogler & Simpson 1995, and many others), has strongly validated the general lines (and many details) of Dahlgren's arrangement. The most recent synthesis (Kubitzki 1998a) is followed as the basis for familial and generic taxonomy of the lilies and their relatives (see summary below). References: Angiosperm Phylogeny Group (1998, 2003); Tamura in Kubitzki (1998a). Our “liliaceous” genera (members of orders placed in the Lilianae) are therefore divided as shown below, largely following Kubitzki (1998a) and some more recent molecular analyses. ALISMATALES TOFIELDIACEAE: Pleea, Tofieldia. LILIALES ALSTROEMERIACEAE: Alstroemeria COLCHICACEAE: Colchicum, Uvularia. LILIACEAE: Clintonia, Erythronium, Lilium, Medeola, Prosartes, Streptopus, Tricyrtis, Tulipa. MELANTHIACEAE: Amianthium, Anticlea, Chamaelirium, Helonias, Melanthium, Schoenocaulon, Stenanthium, Veratrum, Toxicoscordion, Trillium, Xerophyllum, Zigadenus. -
Algal Sex Determination and the Evolution of Anisogamy James Umen, Susana Coelho
Algal Sex Determination and the Evolution of Anisogamy James Umen, Susana Coelho To cite this version: James Umen, Susana Coelho. Algal Sex Determination and the Evolution of Anisogamy. Annual Review of Microbiology, Annual Reviews, 2019, 73 (1), 10.1146/annurev-micro-020518-120011. hal- 02187088 HAL Id: hal-02187088 https://hal.sorbonne-universite.fr/hal-02187088 Submitted on 17 Jul 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Annu. Rev. Microbiol. 2019. 73:X–X https://doi.org/10.1146/annurev-micro-020518-120011 Copyright © 2019 by Annual Reviews. All rights reserved Umen • Coelho www.annualreviews.org • Algal Sexes and Mating Systems Algal Sex Determination and the Evolution of Anisogamy James Umen1 and Susana Coelho2 1Donald Danforth Plant Science Center, St. Louis, Missouri 63132, USA; email: [email protected] 2Sorbonne Université, UPMC Université Paris 06, CNRS, Algal Genetics Group, UMR 8227, Integrative Biology of Marine Models, Station Biologique de Roscoff, CS 90074, F-29688, Roscoff, France [**AU: Please write the entire affiliation in French or write it all in English, rather than a combination of English and French**] ; email: [email protected] Abstract Algae are photosynthetic eukaryotes whose taxonomic breadth covers a range of life histories, degrees of cellular and developmental complexity, and diverse patterns of sexual reproduction. -
Pollination and Evolution of Plant and Insect Interaction JPP 2017; 6(3): 304-311 Received: 03-03-2017 Accepted: 04-04-2017 Showket a Dar, Gh
Journal of Pharmacognosy and Phytochemistry 2017; 6(3): 304-311 E-ISSN: 2278-4136 P-ISSN: 2349-8234 Pollination and evolution of plant and insect interaction JPP 2017; 6(3): 304-311 Received: 03-03-2017 Accepted: 04-04-2017 Showket A Dar, Gh. I Hassan, Bilal A Padder, Ab R Wani and Sajad H Showket A Dar Parey Sher-e-Kashmir University of Agricultural Science and Technology, Shalimar, Jammu Abstract and Kashmir-India Flowers exploit insects to achieve pollination; at the same time insects exploit flowers for food. Insects and flowers are a partnership. Each insect group has evolved different sets of mouthparts to exploit the Gh. I Hassan food that flowers provide. From the insects' point of view collecting nectar or pollen is rather like fitting Sher-e-Kashmir University of a key into a lock; the mouthparts of each species can only exploit flowers of a certain size and shape. Agricultural Science and This is why, to support insect diversity in our gardens, we need to plant a diversity of suitable flowers. It Technology, Shalimar, Jammu is definitely not a case of 'one size fits all'. While some insects are generalists and can exploit a wide and Kashmir-India range of flowers, others are specialists and are quite particular in their needs. In flowering plants, pollen grains germinate to form pollen tubes that transport male gametes (sperm cells) to the egg cell in the Bilal A Padder embryo sac during sexual reproduction. Pollen tube biology is complex, presenting parallels with axon Sher-e-Kashmir University of guidance and moving cell systems in animals. -
Pollination of Cultivated Plants in the Tropics 111 Rrun.-Co Lcfcnow!Cdgmencle
ISSN 1010-1365 0 AGRICULTURAL Pollination of SERVICES cultivated plants BUL IN in the tropics 118 Food and Agriculture Organization of the United Nations FAO 6-lina AGRICULTUTZ4U. ionof SERNES cultivated plans in tetropics Edited by David W. Roubik Smithsonian Tropical Research Institute Balboa, Panama Food and Agriculture Organization of the United Nations F'Ø Rome, 1995 The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. M-11 ISBN 92-5-103659-4 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying or otherwise, without the prior permission of the copyright owner. Applications for such permission, with a statement of the purpose and extent of the reproduction, should be addressed to the Director, Publications Division, Food and Agriculture Organization of the United Nations, Viale delle Terme di Caracalla, 00100 Rome, Italy. FAO 1995 PlELi. uion are ted PlauAr David W. Roubilli (edita Footli-anal ISgt-iieulture Organization of the Untled Nations Contributors Marco Accorti Makhdzir Mardan Istituto Sperimentale per la Zoologia Agraria Universiti Pertanian Malaysia Cascine del Ricci° Malaysian Bee Research Development Team 50125 Firenze, Italy 43400 Serdang, Selangor, Malaysia Stephen L. Buchmann John K. S. Mbaya United States Department of Agriculture National Beekeeping Station Carl Hayden Bee Research Center P. -
Reproduction in Fungi: Genetical and Physiological Aspects by CHARLES G
J. Genet., Vol. 73, Number 1, April 1994, pp. 55-56. (~) Printed in India. BOOK REVIEW Reproduction in Fungi: Genetical and Physiological Aspects By CHARLES G. ELLIOTT; Chapman & Hall, London, 1994; 310 pages; s 35.00 It is now ahnost one hundred years since Klebs (1986)laid the foundation of a scientific approach to the study of reproduction in fungi. Since then an extensive literature has accumulated on reproduction in fungi. To present this information ill terms of principles and concepts and to highlight the immediate problems for study is a daunting task. C. G. Elliott has made a commendable attempt in presenting an overview of the genetical and physiological aspects of fungal reproduction. Fungi are remarkable for producing many kinds of reproductive structures in many ways. They produce spores both asexually and sexually. A single fungus produces a single kind of sexual spore: oospores in phycomycetes, ascospores in ascmnycetes and basidiospores in basidiomycetes. The underlying genetical and physiological mechanisms in the formation of spores are complex and we are only beginning to discern them. The introductory chapter examines the advantages of both asexual and sexual reproduction and the persistence of sex in the face of the apparent advantage of asexual reproduction. The reader is reminded that sexual reproduction in fungi not only serves to generate variability, but also provides a means of repairing damaged DNA. Moreover, it can give rise to propagules resistant to unfavourable environmental conditions. In the chapters that follow, one learns that superimposed on the basic event of nuclear fusion are a variety of regulating medhanisms, the effects of which are to determine a successful mating. -
Fisher Vs. the Worms: Extraordinary Sex Ratios in Nematodes and the Mechanisms That Produce Them
cells Review Fisher vs. the Worms: Extraordinary Sex Ratios in Nematodes and the Mechanisms that Produce Them Justin Van Goor 1,* , Diane C. Shakes 2 and Eric S. Haag 1 1 Department of Biology, University of Maryland, College Park, MD 20742, USA; [email protected] 2 Department of Biology, William and Mary, Williamsburg, VA 23187, USA; [email protected] * Correspondence: [email protected] Abstract: Parker, Baker, and Smith provided the first robust theory explaining why anisogamy evolves in parallel in multicellular organisms. Anisogamy sets the stage for the emergence of separate sexes, and for another phenomenon with which Parker is associated: sperm competition. In outcrossing taxa with separate sexes, Fisher proposed that the sex ratio will tend towards unity in large, randomly mating populations due to a fitness advantage that accrues in individuals of the rarer sex. This creates a vast excess of sperm over that required to fertilize all available eggs, and intense competition as a result. However, small, inbred populations can experience selection for skewed sex ratios. This is widely appreciated in haplodiploid organisms, in which females can control the sex ratio behaviorally. In this review, we discuss recent research in nematodes that has characterized the mechanisms underlying highly skewed sex ratios in fully diploid systems. These include self-fertile hermaphroditism and the adaptive elimination of sperm competition factors, facultative parthenogenesis, non-Mendelian meiotic oddities involving the sex chromosomes, and Citation: Van Goor, J.; Shakes, D.C.; Haag, E.S. Fisher vs. the Worms: environmental sex determination. By connecting sex ratio evolution and sperm biology in surprising Extraordinary Sex Ratios in ways, these phenomena link two “seminal” contributions of G. -
S41467-021-25308-W.Pdf
ARTICLE https://doi.org/10.1038/s41467-021-25308-w OPEN Phylogenomics of a new fungal phylum reveals multiple waves of reductive evolution across Holomycota ✉ ✉ Luis Javier Galindo 1 , Purificación López-García 1, Guifré Torruella1, Sergey Karpov2,3 & David Moreira 1 Compared to multicellular fungi and unicellular yeasts, unicellular fungi with free-living fla- gellated stages (zoospores) remain poorly known and their phylogenetic position is often 1234567890():,; unresolved. Recently, rRNA gene phylogenetic analyses of two atypical parasitic fungi with amoeboid zoospores and long kinetosomes, the sanchytrids Amoeboradix gromovi and San- chytrium tribonematis, showed that they formed a monophyletic group without close affinity with known fungal clades. Here, we sequence single-cell genomes for both species to assess their phylogenetic position and evolution. Phylogenomic analyses using different protein datasets and a comprehensive taxon sampling result in an almost fully-resolved fungal tree, with Chytridiomycota as sister to all other fungi, and sanchytrids forming a well-supported, fast-evolving clade sister to Blastocladiomycota. Comparative genomic analyses across fungi and their allies (Holomycota) reveal an atypically reduced metabolic repertoire for sanchy- trids. We infer three main independent flagellum losses from the distribution of over 60 flagellum-specific proteins across Holomycota. Based on sanchytrids’ phylogenetic position and unique traits, we propose the designation of a novel phylum, Sanchytriomycota. In addition, our results indicate that most of the hyphal morphogenesis gene repertoire of multicellular fungi had already evolved in early holomycotan lineages. 1 Ecologie Systématique Evolution, CNRS, Université Paris-Saclay, AgroParisTech, Orsay, France. 2 Zoological Institute, Russian Academy of Sciences, St. ✉ Petersburg, Russia. 3 St. -
Plant Kingdom Dpp. No.-03
BIOLOGY Daily Practice Problems MEDICAL ENTRANCE - 2020 CLASS : XI TOPIC : PLANT KINGDOM DPP. NO.-03 SECTION - A Q.1 Identify A, B, C, D & E in given diagram. Answer : A. ________ A B. ________ C. ________ D. ________ B E. ________ C D E Q.2 Identify A, B & C in given diagram. Answer : A A. ________ B. ________ C. ________ B C Q.3 Identify A, B & C in given diagram. Answer : A. ________ B. ________ C. ________ A B C Q.4 (i) Identify A & B. (ii) Which stage show by part (1) & (2) Answer : A A. ________ B B. ________ (1) (2) Q.5 (i) Identify A & B in given diagram. (ii) What is syngamy. A Answer : A. ________ B. ________ (1) B (2) Q.6 Identify A, B & C in given diagram. Answer : B A. ________ B. ________ A C. ________ SECTION - B Q.7 The sporophytes bear sporangia that are subtended by leaf-like appendages called ________. Q.8 In majority of the pteridophytes all the spores are of similar kinds; such plants are called ________. Q.9 The cones bearing megasporophylls with ovules or ________ are called macrosporangiate or ________. Q.10 The nucellus is protected by envelopes and the composite structure is called an ________. Q.11 Unlike the gymnosperms where the ovules are naked, in the angiosperms or flowering plants, the pollen grains and ovules are developed in specialised structures called ________. Q.12 Within ovules are present highly reduced female gametophytes termed ________. Q.13 The dominant, photosynthetic phase in such plants is the free-living gametophyte. -
Anisogamy, Chance and the Evolution of Sex Roles
Author's personal copy Opinion Anisogamy, chance and the evolution of sex roles 1 2 3 Lukas Scha¨ rer , Locke Rowe and Go¨ ran Arnqvist 1 Evolutionary Biology, Zoological Institute, University of Basel, Vesalgasse 1, CH-4051 Basel, Switzerland 2 Department of Ecology and Evolutionary Biology, University of Toronto, 25 Willcocks St., Toronto, Ont, M5S 3G5, Canada 3 Animal Ecology, Department of Ecology and Evolution, Evolutionary Biology Centre, University of Uppsala, Norbyva¨ gen 18d, SE-752 36 Uppsala, Sweden Recently, several authors have challenged the view that and sex roles. In their view, sex roles arise entirely from anisogamy, the defining feature of the sexes, is an impor- chance, or from sex differences in environment-driven tant determinant of the evolution of sex roles. Sex roles ‘habits of life’, such as encounter rates, mortality schedules are instead suggested to result from chance, or from non- and re-mating rates [17–22]. The differences in these life- heritable differences in life histories of females and males. history and mating traits are assumed to be externally Here, we take issue with these ideas. We note that ran- imposed, arising from the ecological setting that an indi- dom processes alone cannot cause consistent differences vidual or species finds itself in, rather than ultimately between the sexes, and that those differences between being a consequence of anisogamy. Were this to be true, the sexes in life histories that affect the sex roles are sex roles would be variable to the extent that females and themselves the result of sex-specific selection that can males (as defined by anisogamy) would be no more or less ultimately be traced back to anisogamy.