Leaf Blades on Magnolia Floral Buds
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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. -
The Importance of Petiole Structure on Inhabitability by Ants in Piper Sect. Macrostachys (Piperaceae)
Blackwell Publishing LtdOxford, UKBOJBotanical Journal of the Linnean Society0024-40742007 The Linnean Society of London? 2007 153•• 181191 Original Article ANT DOMATIA IN PIPER SECT. MACROSTACHYS E. J. TEPE ET AL. Botanical Journal of the Linnean Society, 2007, 153, 181–191. With 3 figures The importance of petiole structure on inhabitability by ants in Piper sect. Macrostachys (Piperaceae) ERIC. J. TEPE*, MICHAEL A. VINCENT and LINDA E. WATSON Department of Botany, Miami University, Oxford, OH 45056, USA Received July 2005; accepted for publication August 2006 Several Central American species of Piper sect. Macrostachys have obligate associations with ants, in which the ant partner derives food and shelter from modified plant structures and, in turn, protects the plant against fungal infection and herbivory. In addition to these obligate ant-plants (i.e. myrmecophytes), several other species in Piper have resident ants only sometimes (facultative), and still other plant species never have resident ants. Sheathing petioles of sect. Macrostachys form the domatia in which ants nest. Myrmecophytes in sect. Macrostachys have tightly closed petiole sheaths with bases that clasp the stem. These sheathing petioles appear to be the single most important plant character in the association between ants and species of sect. Macrostachys. We examined the structure and variation of petioles in these species, and our results indicate that minor modifications in a small number of petiolar characters make the difference between petioles that are suitable for habitation by ants and those that are not. © 2007 The Linnean Society of London, Botanical Journal of the Linnean Society, 2007, 153, 181–191. ADDITIONAL KEYWORDS: ant–plant mutualisms – domatia – myrmecophytes – pearl bodies. -
AXR1 Acts After Lateral Bud Formation to Inhibit Lateral Bud Growth in Arabidopsis
This is a repository copy of AXR1 acts after lateral bud formation to inhibit lateral bud growth in Arabidopsis. White Rose Research Online URL for this paper: https://eprints.whiterose.ac.uk/262/ Article: Stirnberg, P., Leyser, O. and Chatfield, S.P. (1999) AXR1 acts after lateral bud formation to inhibit lateral bud growth in Arabidopsis. Plant Physiology. pp. 839-847. ISSN 0032-0889 Reuse Items deposited in White Rose Research Online are protected by copyright, with all rights reserved unless indicated otherwise. They may be downloaded and/or printed for private study, or other acts as permitted by national copyright laws. The publisher or other rights holders may allow further reproduction and re-use of the full text version. This is indicated by the licence information on the White Rose Research Online record for the item. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ Plant Physiology, November 1999, Vol. 121, pp. 839–847, www.plantphysiol.org © 1999 American Society of Plant Physiologists AXR1 Acts after Lateral Bud Formation to Inhibit Lateral Bud Growth in Arabidopsis1 Petra Stirnberg, Steven P. Chatfield, and H.M. Ottoline Leyser* Department of Biology, University of York, P.O. Box 373, York YO10 5YW, United Kingdom Several mutants with altered auxin sensitivity have been The AXR1 gene of Arabidopsis is required for many auxin re- produced in Arabidopsis. -
Field Identification Guide to WAP Plants 2008 3Rd Ed
The Field Identification Guide to Plants Used in the Wetland Assessment Procedure (WAP) Contributors: Shirley R. Denton, Ph.D. - Biological Research Associates Diane Willis, MS – GPI Southeast, Inc. April 2008 Third Edition (2015 Printing) The Field Identification Guide was prepared by the Southwest Florida Water Management District. Additional copies can be obtained from the District at: Southwest Florida Water Management District Resource Projects Department Ecological Evaluation Section 2379 Broad Street Brooksville, Florida 34604 The Southwest Florida Water Management District (District) does not discriminate on the basis of disability. This nondiscrimination policy involves every aspect of the District’s functions, including access to and participation in the District’s programs and activities. Anyone requiring reasonable accommodation as provided for in the Americans with Disabilities Act should contact the District’s Human Resources Bureau Chief, 2379 Broad St., Brooksville, FL 34604-6899; telephone (352) 796-7211 or 1-800-423-1476 (FL only), ext. 4703; or email [email protected]. If you are hearing or speech impaired, please contact the agency using the Florida Relay Service, 1(800)955-8771 (TDD) or 1(800)955-8770 (Voice). Introduction In 1996, the Florida Legislature directed the Southwest Florida Water Management District (District) to begin the process of establishing Minimum Flows and Levels (MFLs) throughout the District, beginning in Hillsborough, Pasco, and Pinellas counties. MFLs are defined as the flow in watercourses below which significant harm to water resources and ecology of the area would occur, and the level in surface-water bodies and aquifers in which significant harm to the water resources of the area would occur. -
The American Woods
TH E I A N W O O D S A M E R C , EXHIB ITED BY ACTUAL SPECIMENS AND WITH C PIO EXPLANAT RY TEXT O US O , ROM E Y N B H H B A OU G . , . RT IX PA . REPRES ENTI NG TWENTY - FIVE S PEC I ES TWENTY - F I VE S ETS OF S E TI O NS C . LOWVI L LE N Y . U A . s . , , . P U B LI SHED AN D SEC TI O NS PREPARED B Y THE AU THOR . Copy rig ht ninet B Y R O M E WE ED—P RSONS PRI NTING A CC . E L E C TR O TY P E R S A N D P R I N TE R S ALB ANY , N . Y . T O mcfl Q i nzhnt m . i ff 1 Qé ? , P M N F TU S . AR O G FORESTER U . DE T E T UL , A RIC RE , T I X A M E R I C A N W O O D P A R , S , DEDI ATED AS AN EXPRESSION OF HIGHE TE TEE IS C S S M. 743130 EF E T THE ERIE PR AC O S S. The necessity of more generally diffu sed information concerning the variety and importance of ou r forest trees is j u stifi c ati on enou gh for the n w n n appeara ce of this work, especially at this day, he the dema ds of n Forestry in this cou ntry are constantly more and more kee ly felt . -
Patterns of Floral Bud Development in Canes of Erect and Trailing Blackberries
J. AMER. SOC. HORT. SCI. 128(1):3–7. 2003. Patterns of Floral Bud Development in Canes of Erect and Trailing Blackberries Fumiomi Takeda1 U.S. Department of Agriculture, Agricultural Research Service, Appalachian Fruit Research Station, 45 Wiltshire Road, Kearneysville, WV 25430 Bernadine C. Strik and Derek Peacock2 Department of Horticulture, 4017 Agriculture and Life Science Building, Oregon State University, Corvallis, OR 97331 John R. Clark Department of Horticulture, 316 Plant Science Building, University of Arkansas, Fayetteville, AR 72701 ADDITIONAL INDEX WORDS. floral primordia, floricane, inflorescence, microscopy, Rubus ABSTRACT. Flower bud development was studied in ‘Cherokee’, ‘Boysen’, and ‘Marion’ blackberries (Rubus subgenus Rubus Watson). In ‘Cherokee’ (erect type), the transition to reproductive development in buds on the branch canes occurred during September in Arkansas and Oregon. Transitions of buds in the axils of the most basal nodes (proximal to the main cane) and the most distal nodes lagged behind buds in the midsection (about nodes 6 to 10). Along the midsection of branch canes, the buds developed uniformly. In buds of ‘Boysen’ and ‘Marion’ (trailing type), the transition to reproductive development occurred in October and sepal primordia were observed in most buds examined by November. Progression of floral bud development continued into January, but at a slower rate than in autumn. Buds on the main canes (>3 m long) of ‘Boysen’ and ‘Marion’ remained at a more advanced stage of flower bud differentiation than buds on the basal branch canes. In both cultivars, buds from the middle one-third section, and sometimes buds from the bottom one-third section, tended to be more advanced than those buds in the top one-third section during much of the sampling period. -
Vegetative Vs. Reproductive Morphology
Today’s lecture: plant morphology Vegetative vs. reproductive morphology Vegetative morphology Growth, development, photosynthesis, support Not involved in sexual reproduction Reproductive morphology Sexual reproduction Vegetative morphology: seeds Seed = a dormant young plant in which development is arrested. Cotyledon (seed leaf) = leaf developed at the first node of the embryonic stem; present in the seed prior to germination. Vegetative morphology: roots Water and mineral uptake radicle primary roots stem secondary roots taproot fibrous roots adventitious roots Vegetative morphology: roots Modified roots Symbiosis/parasitism Food storage stem secondary roots Increase nutrient Allow dormancy adventitious roots availability Facilitate vegetative spread Vegetative morphology: stems plumule primary shoot Support, vertical elongation apical bud node internode leaf lateral (axillary) bud lateral shoot stipule Vegetative morphology: stems Vascular tissue = specialized cells transporting water and nutrients Secondary growth = vascular cell division, resulting in increased girth Vegetative morphology: stems Secondary growth = vascular cell division, resulting in increased girth Vegetative morphology: stems Modified stems Asexual (vegetative) reproduction Stolon: above ground Rhizome: below ground Stems elongating laterally, producing adventitious roots and lateral shoots Vegetative morphology: stems Modified stems Food storage Bulb: leaves are storage organs Corm: stem is storage organ Stems not elongating, packed with carbohydrates Vegetative -
Manual of Leaf Architecture
Manual of Leaf Architecture Morphological description and categorization of dicotyledonous and net-veined monocotyledonous angiosperms - 1 - ©1999 by Smithsonian Institution. All rights reserved. Published and distributed by: Leaf Architecture Working Group c/o Scott Wing Department of Paleobiology Smithsonian Institution 10th St. & Constitution Ave., N.W. Washington, DC 20560-0121 ISBN 0-9677554-0-9 Please cite as: Manual of Leaf Architecture - morphological description and categorization of dicotyledonous and net-veined monocotyledonous angiosperms by Leaf Architecture Working Group. 65p. Paper copies of this manual were printed privately in Washington, D.C. We gratefully acknowledge funding from Michael Sternberg and Jan Hartford for the printing of this manual. - 2 - Names and addresses of the Leaf Architecture Working Group in alphabetical order: Amanda Ash Beth Ellis Department of Paleobiology 1276 Cavan St. Smithsonian Institution NHB Boulder, CO 80303 10th St. & Constitution Ave, N.W. Telephone: 303 666-9534 Washington, DC 20560-0121 Email: [email protected] Telephone: 202 357-4030 Fax: 202 786-2832 Email: [email protected] Leo J. Hickey Kirk Johnson Division of Paleobotany Department of Earth and Space Sciences Peabody Museum of Natural History Denver Museum of Natural History Yale University 2001 Colorado Boulevard 170 Whitney Avenue, P.O. Box 208118 Denver, CO 80205-5798 New Haven, CT 06520-8118 Telephone: 303 370-6448 Telephone: 203 432-5006 Fax: 303 331-6492 Fax: 203 432-3134 Email: [email protected] Email: [email protected] Peter Wilf Scott Wing University of Michigan Department of Paleobiology Museum of Paleontology Smithsonian Institution NHB 1109 Geddes Road 10th St. & Constitution Ave, N.W. -
Spring Wildflowers
BLUE / VIOLET (CONTINUED) GLOSSARY (CONTINUED) Lindenwood Wildflowers Phlox (Polemoniaceae) • Corolla : the showy inner floral envelope; the segments (called • Greek Valerian (Polemonium reptans ): similar to Jacob’s-ladder petals) may be separate or joined. The wildflowers listed below are those that are most common and but stem weaker and fewer leaflets; stamens do not project • Disk (in composites): the round or button-like center (like in a daisy) Spring most-likely to be seen by park visitors; all species listed have been beyond flower. Native. April – June composed of numerous tubular disk flowers, usually surrounded by observed at the preserve in the past. Species are arranged by a circle of ray flowers. prominent flower color and then by Family. The months that are listed are the average blooming periods in this region for the flower. Snapdragon (Scrophulariaceae) • Floweret : the individual flowers of a composite/aster flower head. See the glossary for any obscure technical vocabulary included in • Thyme-leaved Speedwell (Veronica serpyllifolia ): creeping with • Head : a crowded cluster of stalk-less, or nearly stalk-less, flowers. the descriptions. A (*) located after the Family name indicates that small, 4-petaled flowers; leaves are small, opposite, toothless, • Leaflets : the smaller, individual parts of a compound leaf. Wildflowers certain general family characteristics were given in a previous color short-stalked and oval. Alien. May – Sept. • Lobed (leaf): Indented, with outer projections rounded. section. Note: edibility is not included; for your own benefit, DO • Native : originally from this area; not introduced. Violet (Violaceae) NOT ATTEMPT TO INGEST ANY WILD PLANT. • Opposite (leaves, etc.): arranged directly across from each other. -
Axillary Bud Banks of Two Semiarid Perennial Grasses: Occurrence, Longevity, and Contribution to Population Persistence
Oecologia (1997) 110:584±591 Ó Springer-Verlag 1997 J.R. Hendrickson á D.D. Briske Axillary bud banks of two semiarid perennial grasses: occurrence, longevity, and contribution to population persistence Received: 12 August 1996 / Accepted: 30 December 1996 Abstract The occurrence, longevity, and contribution of modifying population structure of these two species. Bud axillary bud banks to population maintenance were number per square meter for B. curtipendula was 25% investigated in a late-seral perennial grass, Bouteloua lower in the long-term grazed compared to the long-term curtipendula, and a mid-seral perennial grass, Hilaria ungrazed community based on a reduction in both tiller belangeri, in a semiarid oak-juniper savanna. Axillary number per plant and plant number per square meter. In buds of both species were evaluated over a 2-year period contrast, bud number per square meter for H. belangeri in communities with contrasting histories of grazing by was 190% greater in the long-term grazed than in the domestic herbivores. A double staining procedure uti- long-term ungrazed community based on a large increase lizing triphenyl tetrazolium chloride and Evan's blue in plant density per square meter. Minimal contributions indicated that both viable and dormant axillary buds of axillary bud banks to annual maintenance of tiller remained attached to the base of reproductive parental populations in this mid- and late-seral species under- tillers for 18±24 months which exceeded parental tiller scores the ecological importance of consistent tiller re- longevity by approximately 12 months. Bud longevity of cruitment from recently developed axillary buds. -
Foliar and Petiole Anatomy of Pterygota (Sterculioideae; Malvaceae) Species and Their Distribution in Nigeria
Anales de Biología 39: 103-109, 2017 ARTICLE DOI: http://dx.doi.org/10.6018/analesbio.39.12 Foliar and petiole anatomy of Pterygota (Sterculioideae; Malvaceae) species and their distribution in Nigeria Emmanuel Chukwudi Chukwuma, Luke Temitope Soyewo, Tolulope Fisayo Okanlawon & Omokafe Alaba Ugbogu Forest Herbarium Ibadan (FHI), Forestry Research Institute of Nigeria, Jericho Hill, Ibadan, Oyo State, Nigeria. Resumen Correspondence Anatomía foliar y del peciolo de especies de Pterigota EC. Chukwuma (Sterculioideae; Malvaceae) E-mail: [email protected] Se estudió la anatomía foliar y del peciolo de especies de Pterygo- Received: 18 February 2017 ta de Nigeria, proveyendo información sobre su distribución en el Accepted: 26 April 2017 área. Principalmente están distribuidas por el sur de Nigeria, espe- Published on-line: 22 June 2017 cialmente en zonas más húmedas. Los microcaracteres foliares muestran que las especies son hiposteomátcas y generalmente paracíticas, más abundantes en P. berquaertii, con un promedio de 115/mm2, que en P. macrocarpa, con 59/mm². Las células epidér- micas son irregulares, rectangulares y poligonales. El peciolo esfé- rico con epidermis uniseriada; la distribución celular varia desde solitarias a radiales múltiples. Este estudio ha proporcionado im- portante información sobre las especies indígenas. Son necesarios estudios posteriores para comprender grado y tiempo de evolución independiente de las especies en Nigeria. Palabras clave: Pterygota, Taxonomía, Foliar, Peciolo, Micro- morfología, Conservación. Abstract Leaf and petiole anatomy of Pterygota species in Nigeria were studied and their distribution within the area is also reported, follow- ing outlined standard protocols. They are chiefly distributed in Southern Nigeria especially in wetter areas. -
Leaf and Petiole Micro-Anatomical Diversities in Some Selected Nigerian Species of Combretum Loefl.: the Significance in Species Identification at Vegetative State
ABMJ 2020, 3(1): 15-29 DOI: 10.2478/abmj-2020-0002 Acta Biologica Marisiensis LEAF AND PETIOLE MICRO-ANATOMICAL DIVERSITIES IN SOME SELECTED NIGERIAN SPECIES OF COMBRETUM LOEFL.: THE SIGNIFICANCE IN SPECIES IDENTIFICATION AT VEGETATIVE STATE Opeyemi Philips AKINSULIRE1*, Olaniran Temitope OLADIPO1, Oluwabunmi Christy AKINKUNMI2, Oladipo Ebenezer ADELEYE1, Kole Fredrick ADELALU1,3 *1Department of Botany, Obafemi Awolowo University, Ile – Ife, Nigeria 2Department of Microbiology, Federal University of Technology, Akure, Nigeria 3Biosystematics and Evolution Laboratory, Chinese Academy of Science, Wuhan Botanical Garden, China *Correspondence: Opeyemi Philips AKINSULIRE [email protected], [email protected] Received: 21 April 2020; Accepted: 06 June 2020; Published: 30 June 2020 Abstract: Leaf and petiole samples of four Combretum Loefl. species which were identified in the Herbarium (IFE) were investigated anatomically in search of stable taxonomic micro-anatomical attributes to improve our knowledge of identification of members of the genus. Anatomical characters; in particular, upper and lower cuticles and epidermal structures, fibre structures, vascular architectures, petiolar outlines and trichome micro-morphology are good taxonomic tools to identify the taxa. The invariable uniseriate to multiseriate upper and lower epidermis; the absence of trichome in the petiole and the presence of branched trichome in the mid-rib region of C. zenkeri P. Beauv delimit the taxa. Variations in vascular architectures can be used to identify the taxa while some other anatomical features in the genus suggest great taxonomic affinities. However, the artificial key, which was constructed using stable taxonomic characters, is a reliable taxonomic tool for proper identification of the four species and which can as well be employed in separating each of the taxa from their close relatives.