Junior & Senior Horticulture Plant Parts Study Guide
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Flowers and Maturation 3Rd - 5Th Grade
Flowers and Maturation 3rd - 5th Grade Introduction Over 90% of all plants are angiosperms or flowering plants. When you think of flowers, you probably think of a rose, carnation or maybe, a tulip . It is not just flowers that are flowering plants. In the spring and summer, you can find flowers in many places but, many plants have flowers that you never see. The grass in the yard is a flowering plant but, you have probably never seen their flower. They are hidden inside the plant. A plant lives to produce more plants and it needs a flower to do that. Flowers are responsible for producing seeds This lesson will teach you the parts of a flower and how those parts work. Objectives • Students will understand the role of flowers in the life of a plant. • Students will understand the basic parts of a flower. • Students will understand the function of the parts of the flower. • Students will understand seed development. Background First, let us look at the diagram of a flower. Photo provided by: https://www.colourbox.com/vector/a-common-flower-parts-vector-34289070 kansascornstem.com A “perfect flower” has both male and female parts. There are also parts that are not male or female. The sepal are leaves that protect the flower as it grows. They peel back as the flower grows. The petals give many flowers their beauty, but the most important job they have are to attract insects that will help them in the process of producing seeds. You will read more about that later. -
Hamamelis.Pdf
Amer. J. Bot. 77(1): 77-91. 1990. COMPARATIVE ONTOGENY OF THE INFLORESCENCE AND FLOWER OF HAMAMELIS VIRGINIANA AND LOROPETALUM CHINENSE (HAMAMELIDACEAE)' Department of Plant Biology, University of New Hampshire, Durham, New Hampshire 03824 A B S T R A C T A comparative developmental study of the inflorescence and flower of Hamamelis L. (4- merous) and Loropetalum (R. Br.) Oliv. (4-5 merous) was conducted to determine how de- velopment differs in these genera and between these genera and others of the family. Emphasis was placed on determining the types of floral appendages from which the similarly positioned nectaries of Hamamel~sand sterile phyllomes of Loropetalum have evolved. In Hamamelis virginiana L. and H. mollis Oliv. initiation of whorls of floral appendages occurred centripetally. Nectary primordia arose adaxial to the petals soon after the initiation of stamen primordia and before initiation of carpel primordia. In Loropetalum chinense (R. Br.) Oliv. floral appendages did not arise centripetally. Petals and stamens first arose on the adaxial portion, and then on the abaxial portion of the floral apex. The sterile floral appendages (sterile phyllomes of uncertain homology) were initiated adaxial to the petals after all other whorls of floral appendages had become well developed. In all three species, two crescent shaped carpel primordia arose opposite each other and became closely appressed at their margins. Postgenital fusion followed and a falsely bilocular, bicarpellate ovary was formed. Ovule position and development are described. The nectaries ofHamamelisand sterile phyllomes of Loropetalum rarely develop as staminodia, suggesting a staminodial origin. However, these whorls arise at markedly different times and are therefore probably not derived from the same whorl of organs in a common progenitor. -
Plant Terminology
PLANT TERMINOLOGY Plant terminology for the identification of plants is a necessary evil in order to be more exact, to cut down on lengthy descriptions, and of course to use the more professional texts. I have tried to keep the terminology in the database fairly simple but there is no choice in using many descriptive terms. The following slides deal with the most commonly used terms (more specialized terms are given in family descriptions where needed). Professional texts vary from fairly friendly to down-right difficult in their use of terminology. Do not be dismayed if a plant or plant part does not seem to fit any given term, or that some terms seem to be vague or have more than one definition – that’s life. In addition this subject has deep historical roots and plant terminology has evolved with the science although some authors have not. There are many texts that define and illustrate plant terminology – I use Plant Identification Terminology, An illustrated Glossary by Harris and Harris (see CREDITS) and others. Most plant books have at least some terms defined. To really begin to appreciate the diversity of plants, a good text on plant systematics or Classification is a necessity. PLANT TERMS - Typical Plant - Introduction [V. Max Brown] Plant Shoot System of Plant – stem, leaves and flowers. This is the photosynthetic part of the plant using CO2 (from the air) and light to produce food which is used by the plant and stored in the Root System. The shoot system is also the reproductive part of the plant forming flowers (highly modified leaves); however some plants also have forms of asexual reproduction The stem is composed of Nodes (points of origin for leaves and branches) and Internodes Root System of Plant – supports the plant, stores food and uptakes water and minerals used in the shoot System PLANT TERMS - Typical Perfect Flower [V. -
Auxin Regulation Involved in Gynoecium Morphogenesis of Papaya Flowers
Zhou et al. Horticulture Research (2019) 6:119 Horticulture Research https://doi.org/10.1038/s41438-019-0205-8 www.nature.com/hortres ARTICLE Open Access Auxin regulation involved in gynoecium morphogenesis of papaya flowers Ping Zhou 1,2,MahparaFatima3,XinyiMa1,JuanLiu1 and Ray Ming 1,4 Abstract The morphogenesis of gynoecium is crucial for propagation and productivity of fruit crops. For trioecious papaya (Carica papaya), highly differentiated morphology of gynoecium in flowers of different sex types is controlled by gene networks and influenced by environmental factors, but the regulatory mechanism in gynoecium morphogenesis is unclear. Gynodioecious and dioecious papaya varieties were used for analysis of differentially expressed genes followed by experiments using auxin and an auxin transporter inhibitor. We first compared differential gene expression in functional and rudimentary gynoecium at early stage of their development and detected significant difference in phytohormone modulating and transduction processes, particularly auxin. Enhanced auxin signal transduction in rudimentary gynoecium was observed. To determine the role auxin plays in the papaya gynoecium, auxin transport inhibitor (N-1-Naphthylphthalamic acid, NPA) and synthetic auxin analogs with different concentrations gradient were sprayed to the trunk apex of male and female plants of dioecious papaya. Weakening of auxin transport by 10 mg/L NPA treatment resulted in female fertility restoration in male flowers, while female flowers did not show changes. NPA treatment with higher concentration (30 and 50 mg/L) caused deformed flowers in both male and female plants. We hypothesize that the occurrence of rudimentary gynoecium patterning might associate with auxin homeostasis alteration. Proper auxin concentration and auxin homeostasis might be crucial for functional gynoecium morphogenesis in papaya flowers. -
Transcript Profiling of a Novel Plant Meristem, the Monocot Cambium
Journal of Integrative JIPB Plant Biology Transcript profiling of a novel plant meristem, the monocot cambiumFA Matthew Zinkgraf1,2, Suzanne Gerttula1 and Andrew Groover1,3* 1. US Forest Service, Pacific Southwest Research Station, Davis, California, USA 2. Department of Computer Science, University of California, Davis, USA 3. Department of Plant Biology, University of California, Davis, USA Article *Correspondence: Andrew Groover ([email protected]) doi: 10.1111/jipb.12538 Abstract While monocots lack the ability to produce a xylem tissues of two forest tree species, Populus Research vascular cambium or woody growth, some monocot trichocarpa and Eucalyptus grandis. Monocot cambium lineages evolved a novel lateral meristem, the monocot transcript levels showed that there are extensive overlaps cambium, which supports secondary radial growth of between the regulation of monocot cambia and vascular stems. In contrast to the vascular cambium found in woody cambia. Candidate regulatory genes that vary between the angiosperm and gymnosperm species, the monocot monocot and vascular cambia were also identified, and cambium produces secondary vascular bundles, which included members of the KANADI and CLE families involved have an amphivasal organization of tracheids encircling a in polarity and cell-cell signaling, respectively. We suggest central strand of phloem. Currently there is no information that the monocot cambium may have evolved in part concerning the molecular genetic basis of the develop- through reactivation of genetic mechanisms involved in ment or evolution of the monocot cambium. Here we vascular cambium regulation. report high-quality transcriptomes for monocot cambium Edited by: Chun-Ming Liu, Institute of Crop Science, CAAS, China and early derivative tissues in two monocot genera, Yucca Received Feb. -
Parts of a Plant Packet - Parts of a Plant Notes - Parts of a Plant Notes Key - Parts of a Plant Labeling Practice
Parts of a Plant Packet - Parts of a Plant Notes - Parts of a Plant Notes Key - Parts of a Plant Labeling Practice Includes Vocabulary: Stigma Stamen Leaf Style Petal Stoma Ovary Receptacle Cuticle Ovule Sepal Shoot System Pistil Xylem Root Hairs Anther Phloem Roots Filament Stem Root System Parts of a Plant Notes 18 14 13 (inside; for food) 15 12 (inside; for water) 16, these are 19 massively out of proportion… 21 17, covering 20 Picture modified from http://www.urbanext.uiuc.edu/gpe/index.html 1. __________- sticky part of the pistil that pollen sticks to 2. __________-long outgrowth of the ovary that collects pollen from the stamens 3. __________- base part of the pistil that holds the ovules 4. __________- unfertilized seed of the plant 5. __________- female part of the flower that contains the stigma, style, ovary and ovules. 6. __________- part of the flower that holds the pollen 7. __________- long thread-like part of the flower that holds the anthers out so insects can get to the pollen. 8. __________- male part of the flower that contains the anther and the filament. 9. __________- colorful part of the flower that protects the flower and attracts insects and other pollinators. 10. __________- stalk that bears the flower parts 11. __________- part that covers the outside of a flower bud to protect the flower before it opens 12. _________- transports water. 13. _________- transports food 14. _________- transport and support for the plant. 15. _________- cells of this perform photosynthesis. 16. _________-holes in the leaf which allow CO2 in and O2 and H2O out. -
A Study of Morphophysiological Descriptors of Cultivated Anthurium
HORTSCIENCE 47(9):1234–1240. 2012. 1970s, many more accessions were intro- duced from The Netherlands (Dilbar, 1992). There are no standardized morphophysio- A Study of Morphophysiological logical descriptors for anthurium available in the literature to characterize accessions of Descriptors of Cultivated Anthurium A. andraeanum Hort. or differentiate between them. Furthermore, the introduced acces- andraeanum Hort. sions have not been systematically evaluated for horticultural performance and adaptabil- Winston Elibox and Pathmanathan Umaharan1 ity under local conditions. This information Department of Life Sciences, Faculty of Science and Agriculture, The University is critical for selecting parents for subse- of the West Indies, St. Augustine Campus, College Road, St. Augustine, Republic quent studies and for embarking on a breed- ing program. of Trinidad and Tobago The objective of the study was to deter- Additional index words. coefficient of variation, correlation, descriptors, frequency distribu- mine useful morphophysiological descriptors tion, index of differentiation, showiness, principal component analysis for horticultural characterization of cultivated anthurium accessions as well as to identify a Abstract. Sixteen morphophysiological parameters of horticultural importance were promising ideotype for breeding purposes. investigated in 82 anthurium accessions grown in the Caribbean. The spathe colors included red, pink, white, green, orange, purple, coral, and brown and obake types with Materials and Methods red, pink, and white spathe colors accounting for 63.4% of the accessions. There was wider variation in spadix color combinations than spathe color. There was wide variation Location. The experiment was conducted for the cut flower and leaf parameters evaluated with productivity and peduncle length in a commercial farm, Kairi Blooms Ltd., having the smallest and largest range, respectively. -
Tansley Review Evolution of Development of Vascular Cambia and Secondary Growth
New Phytologist Review Tansley review Evolution of development of vascular cambia and secondary growth Author for correspondence: Rachel Spicer1 and Andrew Groover2 Andrew Groover 1The Rowland Institute at Harvard, Cambridge, MA, USA; 2Institute of Forest Genetics, Pacific Tel: +1 530 759 1738 Email: [email protected] Southwest Research Station, USDA Forest Service, Davis, CA, USA Received: 29 December 2009 Accepted: 14 February 2010 Contents Summary 577 V. Evolution of development approaches for the study 587 of secondary vascular growth I. Introduction 577 VI. Conclusions 589 II. Generalized function of vascular cambia and their 578 developmental and evolutionary origins Acknowledgements 589 III. Variation in secondary vascular growth in angiosperms 581 References 589 IV. Genes and mechanisms regulating secondary vascular 584 growth and their evolutionary origins Summary New Phytologist (2010) 186: 577–592 Secondary growth from vascular cambia results in radial, woody growth of stems. doi: 10.1111/j.1469-8137.2010.03236.x The innovation of secondary vascular development during plant evolution allowed the production of novel plant forms ranging from massive forest trees to flexible, Key words: forest trees, genomics, Populus, woody lianas. We present examples of the extensive phylogenetic variation in sec- wood anatomy, wood formation. ondary vascular growth and discuss current knowledge of genes that regulate the development of vascular cambia and woody tissues. From these foundations, we propose strategies for genomics-based research in the evolution of development, which is a next logical step in the study of secondary growth. I. Introduction this pattern characterizes most extant forest trees, significant variation exists among taxa, ranging from extinct woody Secondary vascular growth provides a means of radially lycopods and horsetails with unifacial cambia (Cichan & thickening and strengthening plant axes initiated during Taylor, 1990; Willis & McElwain, 2002), to angiosperms primary, or apical growth. -
Non-Destructive Estimation of Root Pressure Using Sap Flow, Stem
Annals of Botany 111: 271–282, 2013 doi:10.1093/aob/mcs249, available online at www.aob.oxfordjournals.org Non-destructive estimation of root pressure using sap flow, stem diameter measurements and mechanistic modelling Tom De Swaef*, Jochen Hanssens, Annelies Cornelis and Kathy Steppe Faculty of Bioscience Engineering, Department of Applied Ecology and Environmental Biology, Laboratory of Plant Ecology, Ghent University, Coupure links 653, B-9000 Ghent, Belgium * For correspondence. E-mail [email protected] Received: 20 August 2012 Returned for revision: 24 September 2012 Accepted: 8 October 2012 Published electronically: 4 December 2012 † Background Upward water movement in plants via the xylem is generally attributed to the cohesion–tension theory, as a response to transpiration. Under certain environmental conditions, root pressure can also contribute Downloaded from to upward xylem water flow. Although the occurrence of root pressure is widely recognized, ambiguity exists about the exact mechanism behind root pressure, the main influencing factors and the consequences of root pres- sure. In horticultural crops, such as tomato (Solanum lycopersicum), root pressure is thought to cause cells to burst, and to have an important impact on the marketable yield. Despite the challenges of root pressure research, progress in this area is limited, probably because of difficulties with direct measurement of root pressure, prompt- ing the need for indirect and non-destructive measurement techniques. http://aob.oxfordjournals.org/ † Methods A new approach to allow non-destructive and non-invasive estimation of root pressure is presented, using continuous measurements of sap flow and stem diameter variation in tomato combined with a mechanistic flow and storage model, based on cohesion–tension principles. -
Chapter 2. Vegetative Morphology of Plants Vegetative Morphology of Plants
Chapter 2. Vegetative morphology of plants Vegetative morphology of plants INTRODUCTION: THE PLANT’S BASIC BODY PLAN Most plants are photosynthetic machines: they capture the energy contained in sunlight and transform solar radiation into chemical energy stored the form of bonds in chains of carbon molecules. Through the process of photosynthesis, light and atmospheric CO2 are combined in the leaves of green plants to form simple carbohydrates, which are then used to build other organic molecules such as cellulose, starch, oils, waxes, proteins, or DNA. Six molecules of CO2 (and some 72 photons of light) are needed to form one molecule of glucose: sunlight 6 CO2 + 6 H2O → C6H12O6 + 6 O2 As a byproduct of the process, six molecules of oxygen are formed and dissipated from the leaf tissue into the atmosphere. To achieve this remarkable feat of turning atmospheric carbon dioxide into living molecules while releasing oxygen into the earth’s atmosphere, plants have evolved highly specialized organs. The light-intercepting structure par excellence is the leaf. The set of leaves in the upper aerial part of the plant form the plant’s canopy, where the plant exchanges gases with the atmosphere and intercepts light from the sun. But in order to work its chemical wonder up in the leaves, the plant also needs water and mineral nutrients such as phosphorus, essential for the synthesis of DNA, or nitrogen, essential for manufacturing proteins. In order to obtain these, plants have developed the root —a complex network of underground stem-like organs— whose role is the absorption of water and mineral nutrients from the soil, and, in doing so, anchoring the plant to the ground. -
Using RNA-Seq to Characterize Pollen–Stigma Interactions for Pollination
www.nature.com/scientificreports OPEN Using RNA‑seq to characterize pollen–stigma interactions for pollination studies Juan Lobaton1,3*, Rose Andrew1, Jorge Duitama2, Lindsey Kirkland1, Sarina Macfadyen3 & Romina Rader1 Insects are essential for the reproduction of pollinator‑dependent crops and contribute to the pollination of 87% of wild plants and 75% of the world’s food crops. Understanding pollen fow dynamics between plants and pollinators is thus essential to manage and conserve wild plants and ensure yields are maximized in food crops. However, the determination of pollen transfer in the feld is complex and laborious. We developed a feld experiment in a pollinator‑dependent crop and used high throughput RNA sequencing (RNA‑seq) to quantify pollen fow by measuring changes in gene expression between pollination treatments across diferent apple (Malus domestica Borkh.) cultivars. We tested three potential molecular indicators of successful pollination and validated these results with feld data by observing single and multiple visits by honey bees (Apis mellifera) to apple fowers and measured fruit set in a commercial apple orchard. The frst indicator of successful outcrossing was revealed via diferential gene expression in the cross‑pollination treatments after 6 h. The second indicator of successful outcrossing was revealed by the expression of specifc genes related to pollen tube formation and defense response at three diferent time intervals in the stigma and the style following cross‑pollination (i.e. after 6, 24, and 48 h). Finally, genotyping variants specifc to donor pollen could be detected in cross‑pollination treatments, providing a third indicator of successful outcrossing. Field data indicated that one or fve fower visits by honey bees were insufcient and at least 10 honey bee fower visits were required to achieve a 25% probability of fruit set under orchard conditions. -
Lecture 30 Origins of Horticultural Science
Lecture 30 1 Lecture 30 Origins of Horticultural Science The origin of horticultural science derives from a confl uence of 3 events: the formation of scientifi c societies in the 17th century, the creation of agricultural and horticultural societies in the 18th century, and the establishment of state-supported agricultural research in the 19th century. Two seminal horticultural societies were involved: The Horticultural Society of London (later the Royal Horticulture Society) founded in 1804 and the Society for Horticultural Science (later the American Society for Horticultural Science) founded in 1903. Three horticulturists can be considered as the Fathers of Horticultural Science: Thomas Andrew Knight, John Lindley, and Liberty Hyde Bailey. Philip Miller (1691–1771) Miller was Gardener to the Worshipful Company of Apothecaries at their Botanic Garden in Chelsea and is known as the most important garden writer of the 18th century. The Gardener’s and Florist’s Diction- ary or a Complete System of Horticulture (1724) was followed by a greatly improved edition entitled, The Gardener’s Dictionary containing the Methods of Cultivating and Improving the Kitchen, Fruit and Flower Garden (1731). This book was translated into Dutch, French, German and became a standard reference for a century in both England and America. In the 7th edition (1759), he adopted the Linnaean system of classifi cation. The edition enlarged by Thomas Martyn (1735–1825), Professor of Botany at Cambridge University, has been considered the largest gardening manual to have ever existed. Miller is credited with introducing about 200 American plants. The 16th edition of one of his books, The Gardeners Kalendar (1775)—reprinted in facsimile edition in 1971 by the National Council of State Garden Clubs—gives direc- tions for gardeners month by month and contains an introduction to the science of botany.