Plant Morphology-I (Root, Stem and Leaf) 12
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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. -
Goethe's Plant Morphology: the Seeds of Evolution
JIDRJournalofInterdisciplinaryResearch Goethe’s Plant Morphology: The Seeds of Evolution TANYA KELLEY It has long been debated whether botanist Carl Linnaeus (1707-1778), and the scientific writing of Johann the continuous view of nature, as Wolfgang von Goethe (1749-1832) exemplified in the work of the English provided the seeds for the theory of naturalist Charles Darwin (1809-1882). evolution. Scholars have argued both Although best known for his sides with equal passion. German literary works, such as Faust, Die Leiden biologist and philosopher, Ernst Haeckel des jungen Werther, and Wilhelm (1834-1919) wrote, “Jean and Lamarck Meister, Goethe was also deeply and Wolfgang Goethe stand at the head involved with the sciences. Some of his of all the great philosophers of nature biographers lament that Goethe’s literary who first established a theory of organic productivity was impeded by all the time development, and who are the illustrious he spent pursuing his interests in fellow workers of Darwin.”1 Taking the comparative anatomy, metallurgy, opposite stance was Chancellor of Berlin meteorology, color theory and botany.3 University, Emil du Bois Reymond Goethe himself said that he valued his (1818-1896). Du Bois was embarrassed work as a scientist more than his poetic by Goethe’s forays into science. He work.4 He pursued a wide range of wrote, “Beside the poet, the scientist interests over the course of his 83 years Goethe fades into the background. Let of life. Until the very end of his life he us at long last put him to rest.”2 I argue was vitally interested in science. -
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. -
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. -
Branching in Nature Jennifer Welborn Amherst Regional Middle School, [email protected]
University of Massachusetts Amherst ScholarWorks@UMass Amherst Patterns Around Us STEM Education Institute 2017 Branching in Nature Jennifer Welborn Amherst Regional Middle School, [email protected] Wayne Kermenski Hawlemont Regional School, [email protected] Follow this and additional works at: https://scholarworks.umass.edu/stem_patterns Part of the Biology Commons, Physics Commons, Science and Mathematics Education Commons, and the Teacher Education and Professional Development Commons Welborn, Jennifer and Kermenski, Wayne, "Branching in Nature" (2017). Patterns Around Us. 2. Retrieved from https://scholarworks.umass.edu/stem_patterns/2 This Article is brought to you for free and open access by the STEM Education Institute at ScholarWorks@UMass Amherst. It has been accepted for inclusion in Patterns Around Us by an authorized administrator of ScholarWorks@UMass Amherst. For more information, please contact [email protected]. Patterns Around Us: Branching in Nature Teacher Resource Page Part A: Introduction to Branching Massachusetts Frameworks Alignment—The Nature of Science • Overall, the key criterion of science is that it provide a clear, rational, and succinct account of a pattern in nature. This account must be based on data gathering and analysis and other evidence obtained through direct observations or experiments, reflect inferences that are broadly shared and communicated, and be accompanied by a model that offers a naturalistic explanation expressed in conceptual, mathematical, and/or mechanical terms. Materials: -
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. -
Mechanical Properties of Blueberry Stems
Vol. 64, 2018 (4): 202–208 Res. Agr. Eng. https://doi.org/10.17221/90/2017-RAE Mechanical properties of blueberry stems Margus Arak1, Kaarel Soots1*, Marge Starast2, Jüri Olt1 1Institute of Technology, Estonian University of Life Sciences, Tartu, Estonia 2Institute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Tartu, Estonia *Corresponding author: [email protected] Abstract Arak M., Soots K., Starast M., Olt J. (2018): Mechanical properties of blueberry stems. Res. Agr. Eng., 64: 202–208. In order to model and optimise the structural parameters of the working parts of agricultural machines, including har- vesting machines, the mechanical properties of the culture harvested must be known. The purpose of this article is to determine the mechanical properties of the blueberry plant’s stem; more precisely the tensile strength and consequent elastic modulus E. In order to achieve this goal, the measuring instrument Instron 5969L2610 was used and accompany- ing software BlueHill 3 was used for analysing the test results. The tested blueberry plant’s stems were collected from the blueberry plantation of the Farm Marjasoo. The diameters of the stems were measured, test units were prepared, tensile tests were performed, tensile strength was determined and the elastic modulus was obtained. Average value of the elastic modulus of the blueberry (Northblue) plant’s stem remained in the range of 1268.27–1297.73 MPa. Keywords: agricultural engineering; blueberry; harvesting; mechanical properties; elastic modulus Lowbush blueberry (Vaccinium angustifolium abandoned peat fields because of soils with high Ait.) is a native naturally occurring plant in North organic matter content and low pH (Yakovlev et America. -
Strategies for Growing a High‐Quality Root System, Trunk, and Crown in a Container Nursery
Strategies for Growing a High‐Quality Root System, Trunk, and Crown in a Container Nursery Companion publication to the Guideline Specifications for Nursery Tree Quality Table of Contents Introduction Section 1: Roots Defects ...................................................................................................................................................................... 1 Liner Development ............................................................................................................................................. 3 Root Ball Management in Larger Containers .......................................................................................... 6 Root Distribution within Root Ball .............................................................................................................. 10 Depth of Root Collar ........................................................................................................................................... 11 Section 2: Trunk Temporary Branches ......................................................................................................................................... 12 Straight Trunk ...................................................................................................................................................... 13 Section 3: Crown Central Leader ......................................................................................................................................................14 Heading and Re‐training -
Morphological Description of Plants: New Perspectives in Development and Evolution
® International Journal of Plant Developmental Biology ©2010 Global Science Books Morphological Description of Plants: New Perspectives in Development and Evolution 1* 2 Emilio Cervantes • Juana G . de Diego 1 IRNASA-CSIC. Apartado 257. 37080. Salamanca. Spain 2 Dept Bioquímica y Biología Molecular. Campus Miguel de Unamuno. Universidad de Salamanca. Spain Corresponding author : * [email protected] ABSTRACT The morphological description of plants has been fundamental in the history of botany and provided the keys for taxonomy. Nevertheless, in biology, a discipline governed by the interest in function and based on reductionist approaches, the analysis of forms has been relegated to second place. Plants contain organs and structures that resemble geometrical forms. Plant ontogeny may be seen as a sequence of growth processes including periods of continuous growth with modification that stop at crucial points often represented by structures of remarkable similarity to geometrical figures. Instead of the tradition in developmental studies giving more importance to animal models, we propose that the modular type of plant development may serve to remark conceptual aspects in that may be useful in studies with animals and contribute to original views of evolution. _____________________________________________________________________________________________________________ Keywords: concepts, description, geometry, structure INTRODUCTION: PLANTS OFFER NEW reflects a more general situation in Biology, a discipline APPROACHES TO DEVELOPMENT that has matured from the experimental protocols and views of biochemistry, where the predominant role of experimen- The study of development is today a major biological disci- tation has contributed to a decline in basic aspects that need pline. Although it was traditionally more focused in animal to be more descriptive, such as those related with mor- systems, increased emphasis in plant development may phology. -
The Genomics of Wood Formation in Angiosperm Trees
The Genomics of Wood Formation in Angiosperm Trees Xinqiang He and Andrew T. Groover Abstract Advances in genomic science have enabled comparative approaches that can evaluate the evolution of genes and mechanisms underlying phenotypic traits relevant to angiosperm forest trees. Wood formation is an excellent subject for com- parative genomics, as it is an ancestral trait for angiosperms and has undergone significant modification in different angiosperm lineages. This chapter discusses some of the traits associated with wood formation, what is currently known about the genes and mechanisms regulating these traits, and how comparative evolution- ary genomic studies can be undertaken to provide more comprehensive views of the evolution and development of wood formation in angiosperms. Keywords Wood formation • Wood development • Wood evolution • Transcriptional regulation • Epigenetics • Comparative genomics Genomic Perspectives on the Evolutionary Origins and Variation in Angiosperm Wood Introduction The evolutionary and developmental biology of wood are fundamental to under- standing the amazing diversification of angiosperms. While flower morphology and reproductive characters associated with angiosperms have been the focus of numer- ous genetic and genomic evo-devo studies, wood development is a relatively neglected trait of angiosperm evolution and development that is now tractable for comparative and evolutionary genomic studies. The ability to produce wood from a X. He School of Life Sciences, Peking University, Beijing 100871, China A.T. Groover (*) Pacific Southwest Research Station, US Forest Service, Davis, 95618 CA, USA Department of Plant Biology, University of California Davis, Davis, 95618 CA, USA e-mail: [email protected] © Springer International Publishing AG 2017 205 A.T. Groover and Q.C.B. -
Perspectives of Branching Pattern and Branching Density in 30 Woody Trees and Shrubs in Tamulipan Thornscrub, Northeast of Mexic
rch: O ea pe es n A R t c s c Maiti et al., Forest Res 2015, 4:4 e e r s o s Forest Research F Open Access DOI: 10.4172/2168-9776.1000160 ISSN: 2168-9776 Research Article Open Access Perspectives of Branching Pattern and Branching Density in 30 Woody Trees and Shrubs in Tamulipan Thornscrub, Northeast of Mexico Maiti R1*, Rodriguez HGM1, Aruna Kumari2 and Díaz JCG1 1Faculty of Forestry, Autonomous University of Nuevo Leon, Carr. Nac. No. 85 Km. 45, Linares, Nuevo Leon 67700, México 2Agricultural College, Telangana State Agricultural University, Polasa, Jagtial, Karimnagar, Telangana, India Abstract In the context of the ecological perspectives, there is growing attention in the modelling of the morphological structure of the plants for developing the model of the functional processes of plants. The branching pattern functions as solar panel in the capture of solar radiation for the production of biomass and timber. The present study undertaken with the objective of determining the density of branching and types of branching of 30 tree species (trees and shrubs of Tamaulipan thorn scrub such; Helietta parvifolia, Sargentia gregii, Guaiacum angustifolium, Ebenopsis ebano, Harvadia pallens, Condalia hoockeri, Zanthoxylum fagara, Cordia boissieri, Acacia berlandieri, Diospyros texana, Celtis pallida, Forestiera angustifolia, Diospyros palmeri, Parkinsonia texana, Acacia farnesiana, Sideroxylon celastrina, Caesalpinia mexicana, Karwinskia humboldtiana, Croton suaveolens, Amyris texana, Leucaena leucocephala, Ehretia anacua, Gymnosperma glutinosum, Celtis laevigata, Acacia rigidula, Acacia shaffneri, Eysenhardtia polystachya, Prosopis laevigata, Bernardia myricifolia and Leucophyllum frutescens located at the experimental field of Forest Science Faculty of Autónoma de Nuevo en Linares, N.L., México has shown a large variability in the density and branching patterns. -
Lab 2: Plant Morphology: Leaves
Lab 2: Leaves 1 Name: ______________________________________ Date/Lab time: _________________ Lab 2: Plant Morphology: Leaves Supplies: Carnivorous plant Leaf types Cactus with needles Simple- Succulent leafed plant Sessile- without petiole Monocots and Dicots Compound- Equisetum Pinnate Mother of 1000’s Palmate Ginkgo , pine, fern, etc. Vocabulary to know: Abaxial surface, Adaxial surface, Blade, Compound leaves, Leaflet, Lobed, Midrib, Palmate compound leaf , Petiole, Phyllotaxis, Pinnate compound leaf , Serrated, Sessile leaves, Simple leaves. Introduction: A leaf is defined by its formation (during its very early stage, a leaf extends over and protects the shoot tip) (google shoot meristem). Find a live shoot tip on a plant supplied in lab. Note that you have to dig through a lot of very young leaves to get to it. This definition holds true for even modified leaves. Look at the shoot tip of the cactus (ouch! don't touch it!). Note the cactus spines (needles) form over the shoot tip, thus needles are leaves, though highly modified. Another common feature of leaves is the presence of axillary buds (see figure on next page). Locate a leave's axillary bud just above the point where the leaf attaches to the stem. Axillary buds have the potential of forming new branches or flowers. Leaf Arraignment on Stem The arraignment of leaves on a branch is called phyllotaxis . Note branches with alternate phyllotaxis (leaves arranged alternately one per node), opposite phyllotaxis (leaves arranged 2 per node) or whorled phyllotaxis (more than 2 leaves per node). Identify plants with these types of phyllotaxis. Whorled phyllotaxis is less common. See sweet woodruff and horsetail ( Equisetum ) for examples.