Biomimetic Engineering Analysis of Heliotropic Plants 36
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Stenospermocarpy Biological Mechanism That Produces Seedlessness in Some Fruits (Many Table Grapes, Watermelon)
Phytohormones The growth and development of a plant are influenced by: •Gene:c factors •External environmental factors •Chemical hormones inside the plant Secondary messengers 1. Involve in the transfer informaon from sources to targets 2. Amplify the signal produced by the phytohormone Phytohormones Plant hormones are organic compounds that are effec:ve at very low concentraon (1g 20,000 tons-1) They interact with specific target :ssues to cause physiological responses •Growth •Fruit ripening Phytohormones •Hormones s:mulate or inhibit plant growth Major groups of hormones: 1. Auxins 2. Gibberellins 3. Ethylene 4. Cytokinins 5. Abscisic acid 6. Brassinostereoids 7. Salicylic acid 8. Polyaminas 9. Jasmonates 10. Systemin 11. Nitric oxide Arabidopsis thaliana Phytohormones EARLY EXPERIMENTS ON PHOTROPISM SHOWED THAT A STIMULUS (LIGHT) RELEASED CHEMICALS THAT INFLUENCED GROWTH Auxins Auxin causes several responses in plants: * Phototropism * Geotropism * Promo:on of apical dominance * Flower formaon * Fruit set and growth * Formaon of adven::ous roots * Differen:aon of vascular :ssues (de novo or repairing existent vascular :ssue) Auxins Addi:on of auxins produce parthenocarpic fruit. Stenospermocarpy Biological mechanism that produces seedlessness in some fruits (many table grapes, watermelon) diploid + tetraploid parent = triploid seeds vegetave parthenocarpy Plants that do not require pollinaon or other s:mulaon to produce parthenocarpic fruit (cucumber) Auxins Synthe:c auxins Widely used in agriculture and hor:culture • prevent leaf abscission • prevent fruit drop • promote flowering and frui:ng • control weeds Agent Orange - 1:1 rao of 2,4-D and 2,4,5-T Dioxin usually contaminates 2,4,5-T, which is linked to miscarriages, birth defects, leukemia, and other types of cancer. -
A Framework for Plant Behavior Author(S): Jonathan Silvertown and Deborah M
A Framework for Plant Behavior Author(s): Jonathan Silvertown and Deborah M. Gordon Reviewed work(s): Source: Annual Review of Ecology and Systematics, Vol. 20 (1989), pp. 349-366 Published by: Annual Reviews Stable URL: http://www.jstor.org/stable/2097096 . Accessed: 10/02/2012 12:56 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. Annual Reviews is collaborating with JSTOR to digitize, preserve and extend access to Annual Review of Ecology and Systematics. http://www.jstor.org Annu. Rev. Ecol. Syst. 1989. 20:349-66 Copyright ? 1989 by Annual Reviews Inc. All rights reserved A FRAMEWORKFOR PLANT BEHAVIOR Jonathan Silvertown' and Deborah M. Gordon2 'BiologyDepartment, Open University, Milton Keynes MK7 6AA, UnitedKingdom 2Departmentof Zoology,University of Oxford,South Parks Rd, Oxford,OXI 3PS, UnitedKingdom INTRODUCTION The language of animalbehavior is being used increasinglyto describecertain plant activities such as foraging (28, 31, 56), mate choice (67), habitatchoice (51), and sex change (9, 10). Furthermore,analytical tools such as game theory, employed to model animal behavior, have also been applied to plants (e.g. 42, 54). There is some question whetherwords used to describe animal behavior, such as the word behavior itself, or foraging, can be properly applied to the activities of plants. -
Plant Physiology
PLANT PHYSIOLOGY Vince Ördög Created by XMLmind XSL-FO Converter. PLANT PHYSIOLOGY Vince Ördög Publication date 2011 Created by XMLmind XSL-FO Converter. Table of Contents Cover .................................................................................................................................................. v 1. Preface ............................................................................................................................................ 1 2. Water and nutrients in plant ............................................................................................................ 2 1. Water balance of plant .......................................................................................................... 2 1.1. Water potential ......................................................................................................... 3 1.2. Absorption by roots .................................................................................................. 6 1.3. Transport through the xylem .................................................................................... 8 1.4. Transpiration ............................................................................................................. 9 1.5. Plant water status .................................................................................................... 11 1.6. Influence of extreme water supply .......................................................................... 12 2. Nutrient supply of plant ..................................................................................................... -
History and Epistemology of Plant Behaviour: a Pluralistic View?
Synthese (2021) 198:3625–3650 https://doi.org/10.1007/s11229-019-02303-9 BIOBEHAVIOUR History and epistemology of plant behaviour: a pluralistic view? Quentin Hiernaux1 Received: 8 June 2018 / Accepted: 24 June 2019 / Published online: 2 July 2019 © Springer Nature B.V. 2019 Abstract Some biologists now argue in favour of a pluralistic approach to plant activities, under- standable both from the classical perspective of physiological mechanisms and that of the biology of behaviour involving choices and decisions in relation to the environ- ment. However, some do not hesitate to go further, such as plant “neurobiologists” or philosophers who today defend an intelligence, a mind or even a plant consciousness in a renewed perspective of these terms. To what extent can we then adhere to pluralism in the study of plant behaviour? How does this pluralism in the study and explanation of plant behaviour fit into, or even build itself up, in a broader history of science? Is it a revolutionary way of rethinking plant behaviour in the twenty-first century or is it an epistemological extension of an older attitude? By proposing a synthesis of the question of plant behaviour by selected elements of the history of botany, the objective is to show that the current plant biology is not unified on the question of behaviour, but that its different tendencies are in fact part of a long botanical tradition with contrasting postures. Two axes that are in fact historically linked will serve as a common thread. 1. Are there several ways of understanding or conceiving plant behaviour within plant sciences and their epistemology? 2. -
Plant Classification and Seeds
Ashley Pearson – Plant Classification and Seeds ● Green and Gorgeous Oxfordshire ● Cut flowers ● Small amounts of veg still grown and sold locally Different Classification Systems Classification by Life Cycle : Ephemeral (6-8 wks) Annual Biennial Perennial Classification by Ecology: Mesophyte, Xerophyte, Hydrophyte, Halophyte, Cryophyte Raunkiaers Life Form System: based on the resting stage Raunkiaers Life Form System Classification contd. Classification by Plant Growth Patterns Monocots vs. Dicots (NB. only applies to flowering plants - angiosperms) Binomial nomenclature e.g., Beetroot = Beta vulgaris Plantae, Angiosperms, Eudicots, Caryophyllales, Amaranthaceae, Betoideae, Beta, Beta vulgaris After morphological characters, scientists used enzymes and proteins to classify plants and hence to determine how related they were via evolution (phylogeny) Present day we use genetic data (DNA, RNA, mDNA, even chloroplast DNA) to produce phylogenetic trees Plant part modifications ● Brassica genus ● ● Roots (swede, turnips) ● Stems (kohl rabi) ● Leaves (cabbages, Brussels Sprouts-buds) ● Flowers (cauliflower, broccoli) ● Seeds (mustards, oil seed rape) Plant hormones / PGR's / phytohormones ● Chemicals present in very low concentrations that promote and influence the growth, development, and differentiation of cells and tissues. ● NB. differences to animal hormones! (no glands, no nervous system, no circulatory system, no specific mode of action) ● Not all plant cells respond to hormones, but those that do are programmed to respond at specific points in their growth cycle ● Five main classes of PGR's ● Abscisic acid (ABA) ● Role in abscission, winter bud dormancy (dormin) ● ABA-mediated signalling also plays an important part in plant responses to environmental stress and plant pathogens ● ABA is also produced in the roots in response to decreased water potential. -
Motion in Plants and Animals SMPK Penabur Jakarta Motion
Motion in Plants and Animals SMPK Penabur Jakarta Motion What is that? Which part? Have you ever see the flying bird? Why they can do stable flying? What affects them? Let’s learn! Plant’s motion Animal’s motion in water, on air, and on land Why so important?? To know and explain motion in living things Important Terms Motion Stimulation Inertia Elasticity Surface Tension Mimosa pudica Have you ever see? Mimosa pudica Response to stimulation If the leaves got stimulation, the water flow will keep away from stimulated area Stimulated area water less, turgor tension less leaves will closed Turgor tension= tension affected by cell contents to wall cell in plant Movement Movement in living system they can change chemical energy to mechanical energy Human and animal active movement Plants have different movement Motion in Plant Growth Reaction to respond stimuli (irritability) Endonom Hygroscopic Etionom PHOTOTROPISM HYDROTROPISM TROPISM GEOTROPISM THIGMOTROPISM ENDONOM RHEOTROPISM PLANT MOTION HYGROSCOPIC ETIONOM PHOTOTAXIS TAXIS CHEMOTAXIS NICTINASTY THIGMONASTY/ NASTIC SEISMONASTY PHOTONASTY COMPLEX A. Endogenous Movement Spontaneusly Not known yet its cause certainly Predicted it caused by stimulus from plant itself Ex: ◦ Movement of cytoplasm in cell ◦ Bending movement of leaf bid because of different growth velocity ◦ Movement of chloroplast Chloroplast movement B. Hygroscopic Movement Caused by the influence of the change of water level from its cell non-homogenous wrinkling Ex: ◦ The breaking of dried fruit of leguminous fruit, such as kacang buncis (Phaseolus vulgaris), kembang merak (Caesalpinia pulcherrima), and Impatiens balsamina (pacar air) and other fruits ◦ The opening of sporangium in fern ◦ Rolled of peristomal gear in moss’ sporangium C. -
Circadian Regulation of Sunflower Heliotropism, Floral Orientation, and Pollinator Visits
Title: Circadian regulation of sunflower heliotropism, floral orientation, and pollinator visits Authors: Hagop S. Atamian1, Nicky M. Creux1, Evan A. Brown2, Austin G. Garner2, Benjamin K. Blackman2,3, and Stacey L. Harmer1* Affiliations: 1Department of Plant Biology, University of California, One Shields Avenue, Davis, CA 95616, USA. 2Department of Biology, University of Virginia, PO Box 400328, Charlottesville, VA 22904, USA. 3Department of Plant and Microbial Biology, University of California, 111 Koshland Hall, Berkeley, CA 94720, USA. *Correspondence to: [email protected]. Abstract: Young sunflower plants track the sun from east to west during the day and then reorient during the night to face east in anticipation of dawn. In contrast, mature plants cease movement with their flower heads facing east. We show that circadian regulation of directional growth pathways accounts for both phenomena and leads to increased vegetative biomass and enhanced pollinator visits to flowers. Solar tracking movements are driven by antiphasic patterns of elongation on the east and west sides of the stem. Genes implicated in control of phototropic growth, but not clock genes, are differentially expressed on the opposite sides of solar tracking stems. Thus interactions between environmental response pathways and the internal circadian oscillator coordinate physiological processes with predictable changes in the environment to influence growth and reproduction. One Sentence Summary: Sun-tracking when young, east-facing when mature, warmer sunflowers attract more pollinators. Text+References+Legends Cover Main Text: Most plant species display daily rhythms in organ expansion that are regulated by complex interactions between light and temperature sensing pathways and the circadian clock (1). These rhythms arise in part because the abundance of growth-related factors such as light signaling components and hormones such as gibberellins and auxins are regulated both by the circadian clock and light (2-4). -
University of Groningen the Thermal Ecology of Flowers Van Der Kooi
University of Groningen The thermal ecology of flowers van der Kooi, Casper J.; Kevan, Peter G.; Koski, Matthew H. Published in: Annals of Botany DOI: 10.1093/aob/mcz073 IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from it. Please check the document version below. Document Version Publisher's PDF, also known as Version of record Publication date: 2019 Link to publication in University of Groningen/UMCG research database Citation for published version (APA): van der Kooi, C. J., Kevan, P. G., & Koski, M. H. (2019). The thermal ecology of flowers. Annals of Botany, 124(3), 343-353. https://doi.org/10.1093/aob/mcz073 Copyright Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons). The publication may also be distributed here under the terms of Article 25fa of the Dutch Copyright Act, indicated by the “Taverne” license. More information can be found on the University of Groningen website: https://www.rug.nl/library/open-access/self-archiving-pure/taverne- amendment. Take-down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum. -
Kinematic Amplification Strategies in Plants and Engineering
Kinematic amplification strategies in plants and engineering Victor Charpentier, Philippe Hannequart, Sigrid Adriaenssens, Olivier Baverel, Emmanuel Viglino, Sasha Eisenman To cite this version: Victor Charpentier, Philippe Hannequart, Sigrid Adriaenssens, Olivier Baverel, Emmanuel Viglino, et al.. Kinematic amplification strategies in plants and engineering. Smart Materials and Structures, IOP Publishing, 2017, 26 (6), pp.63002 - 63002. 10.1088/1361-665X/aa640f. hal-01618277 HAL Id: hal-01618277 https://hal-enpc.archives-ouvertes.fr/hal-01618277 Submitted on 17 Oct 2017 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. Page 1 of 30 AUTHOR SUBMITTED MANUSCRIPT - SMS-104018.R2 1 2 3 Kinematic amplification strategies in plants and engineering 4 5 6 1 2,3 1 2 7 Victor Charpentier* , Philippe Hannequart* , Sigrid Adriaenssens , Olivier Baverel , 3 4 8 Emmanuel Viglino , Sasha Eisenman 9 10 1Department of Civil and Environmental Engineering, Princeton University, Princeton, NJ, USA 11 12 2 Laboratoire Navier, UMR 8205, École des Ponts, IFSTTAR, CNRS, UPE, Champs-sur-Marne, France 13 14 3 Arcora, Ingérop Group, Rueil-Malmaison, France 15 16 4 Department of Landscape Architecture and Horticulture, Temple University, Ambler, PA, USA 17 18 19 *The authors designated have contributed equally to the research and writing of the manuscript 20 21 22 23 Abstract: 24 While plants are primarily sessile at the organismal level, they do exhibit a vast array of 25 movements at the organ or sub-organ level. -
Tamilnadu Board Class 9 Science Chapter 6 Term I
UNIT Living World of Plants - 6 Plant Physiology Learning Objectives At the end of this unit the students will be able to understand, that Plants too have certain autonomic movements how do plants produce their food through the process of photosynthesis? that Plants are the primary producers that feed the rest of the living organisms Introduction (sunflower) follows the path of the sun from dawn to dusk, (from east to west) and Animals move in search of food, shelter and during night it moves from west to east. for reproduction, even microorganisms The dance of Desmodium gyrans (Indian show movement. telegraph plant) leaf is mesmerizing. Do plants show such movement We see a branch of a tree shaking in heavy thunder storm; and leaves dancing in gentle wind. These movements are caused by an external agency. Do they Move on their 6.1 own Accord In short, do plants have spontaneous movements without external agency? Do they breathe? In this chapter we will study some of the biological functions of plants. 6.2 Do Plants Move The leaves of Mimosa pudica (touch-me- not plant) closes on touching, and in like manner, the stalk of Helianthus annuus Mimosa pudica 6 . L i v i ng Wo l d o P a nt P a nt P y s i o og 133 IX_Science Unit-6.indd 133 27-03-2018 12:31:36 Activity 1 Roots grow down and shoots grow up You can do this experiment with some of your friends. Step -1 It is easy and fun. Take four or ve earthen cups or small pots and ll them with soil from a eld. -
Mechanism of the Seismonastic Reaction in Mimosa Pudica' Robert D
Plant Physiol. (1969) 44, 1101-1107 Mechanism of the Seismonastic Reaction in Mimosa pudica' Robert D. .Allen' Biophysics Department, University of California at Los Angeles, Los Angeles, California 90024 Received January 13, 1969. Abstract. The efflux of K+ from the pulvinar cells of Mimosa pudica was shown to inerease substantially during the seismonastic reaction. This result is shown to indicate a decrease in a (reflection coefiicient) of pulvinar cell membrane for potassium salts which could account for the pulvinar cell turgor decrease during the seismonastic reaction. Membrane potentials and concentrations of Ca2+, K+, Cl-, S, and P were measured in the top and bottom halves of pulvini. Pulvinar cells showed a large negative membrane potential, cell vacuole r:lative to external solution, but no significant difference in membrane potential could be detected between upper and lower pulvinar cells. A large difference in K+ and Cl- concentration betwe-n top and bottom pulvinar halves was evident in reactive pulvini but not in unreactive pulvini. The effect of K+ concentration on plant growth and leaf reactivity was also investigated. One of the most fascinating phenomena in the RTAC. Thermodynamic osmotic pressure differ- plant kingdom is the seismonastic, i.e. rapid, leaf ence across the cell membrane. movement exhibited by Mimosa pudica. Movement The reflection coefficient, the relative can be initiated by stimuli such as electrical shock or membrane permeability to solutes and touch, and is effected by the main pulvinus at the water. When of = 1, the membrane is base of the petiole. It is generally accepted that this semipermeable; when C = 0, the mem- stimulus causes a loss of turgor in the cells composing brane is completely nonselective to pas- the lower side of the pulvinus (20) ; the leaf then sage of solutes and water. -
Download E-Book
EVERYMAN’S SCIENCE Vol. L No. 5 (Dec’15 - Jan’16) EDITORIAL ADVISORY BOARD EDITORIAL BOARD Dr. Kaushik Majumdar (Gurgaon) Editor-in-Chief Dr. Ashok Kumar Saxena Prof. Prabhu Nath Pandey (Ranchi) Area Editors Prof. (Dr.) N.K. Saksena (Kanpur) Dr. (Mrs.) Vijay Laxmi Saxena Dr. Rajeev Jain (Gwalior) (Biological Sciences) Dr. Tejender Nath Jowhar (Dehradun) Dr. Pramod Kumar Verma (Earth Sciences, Engineering & Material Sciences) Prof. Asis Mazumdar (Kolkata) Dr. Manoj Kumar Chakrabarti Dr. Gangadhar Mishra (Ranchi) (Medical Sciences including Physiology) Prof. Karbhari Vishwanath Kale Dr. Arvind Kumar Saxena (Aurangabad) (Physical Sciences) Dr. Arvind Kumar Dixit (Kanpur) Dr. (Mrs.) Vipin Sobti (Social Sciences) Dr. Snehashish Chakraverty (Rourkela) General Secretary (Membership Affairs) Prof. (Dr.) Chittaranjan Maity (Kolkata) Dr. Nilangshu Bhushan Basu Prof. Jagdish Rai (Bareilly) General Secretary (Scientific Activities) Prof. Arun Kumar Prof. Dinesh Kumar Maheshwari (Haridwar) Editorial Secretary Dr. Amit Krishna De COVER PHOTOGRAPHS Past General Presidents of ISCA Printed and published by Dr. Ashok Kumar Saxena 1. Dr. Vasant Gowariker (1992) on behalf of Indian Science Congress Association 2. Dr. S. Z. Qasim (1993) and printed at T. C. Dutta Merchants Pvt. Ltd., P- 3. Prof. P. N. Srivastava (1994) 23/24, Radha Bazar Street, Kolkata - 700 001 and 4. Dr. S. C. Pakrashi (1995) published at Indian Science Congress Association, 5. Prof. U. R. Rao (1996) 14, Dr. Biresh Guha Street, Kolkata - 700 017, with Dr. Ashok Kumar Saxena as Editor. 6. Dr. S. K. Joshi (1997) Annual Subscription : (6 issues) For permission to reprint or reproduce any portion of the journal, please write Institutional Þ 500/- ; Individual Þ 300/- to the Editor-in-Chief.