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LECTURE PRESENTATIONS For CAMPBELL BIOLOGY, NINTH EDITION Jane B. Reece, Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Robert B. Jackson Chapter 35 Plant Structure, Growth, and Development Lectures by Erin Barley Kathleen Fitzpatrick © 2011 Pearson Education, Inc. Figure 35.1 The Three Basic Plant Organs: Roots, Stems, and Leaves • Basic morphology of vascular plants reflects their evolution as organisms that draw nutrients from below ground and above ground • Plants take up water and minerals from below ground • Plants take up CO2 and light from above ground © 2011 Pearson Education, Inc. • Three basic organs evolved: roots, stems, and leaves • They are organized into a root system and a shoot system © 2011 Pearson Education, Inc. Figure 35.2 Reproductive shoot (flower) Apical bud Node Internode Apical bud Vegetative shoot Leaf Axillary bud Shoot system Blade Petiole Stem Taproot Lateral (branch) roots Root system • Roots rely on sugar produced by photosynthesis in the shoot system • Shoots rely on water and minerals absorbed by the root system • Monocots and eudicots (dicots) are the two major groups of angiosperms © 2011 Pearson Education, Inc. Roots • A root is an organ with important functions: – Anchoring the plant – Absorbing minerals and water – Storing carbohydrates © 2011 Pearson Education, Inc. • Most eudicots and gymnosperms have a taproot system, which consists of: – A taproot, the main vertical root – Lateral roots, or branch roots, that arise from the taproot • Most monocots have a fibrous root system, which consists of: – Adventitious roots that arise from stems or leaves – Lateral roots that arise from the adventitious roots © 2011 Pearson Education, Inc. • In most plants, absorption of water and minerals occurs near the root hairs, where vast numbers of tiny root hairs increase the surface area © 2011 Pearson Education, Inc. Figure 35.3 • Many plants have root adaptations with specialized functions © 2011 Pearson Education, Inc. Figure 35.4a Prop roots Figure 35.4b Storage roots Figure 35.4c “Strangling” aerial roots Figure 35.4d Pneumatophores Figure 35.4e Buttress roots Figure 35.4 “Strangling” aerial roots Storage roots Prop roots Buttress roots Pneumatophores Stems • A stem is an organ consisting of – An alternating system of nodes, the points at which leaves are attached – Internodes, the stem segments between nodes © 2011 Pearson Education, Inc. • An axillary bud is a structure that has the potential to form a lateral shoot, or branch • An apical bud, or terminal bud, is located near the shoot tip and causes elongation of a young shoot • Apical dominance helps to maintain dormancy in most axillary buds © 2011 Pearson Education, Inc. • Many plants have modified stems (e.g., rhizomes, bulbs, stolons, tubers) © 2011 Pearson Education, Inc. Figure 35.5a Rhizome Root Rhizomes Figure 35.5b Storage leaves Stem Bulbs Figure 35.5c Stolon Stolons Figure 35.5d Tubers Figure 35.5 Rhizomes Rhizome Root Bulbs Storage leaves Stem Stolons Stolon Tubers Leaves • The leaf is the main photosynthetic organ of most vascular plants • Leaves generally consist of a flattened blade and a stalk called the petiole, which joins the leaf to a node of the stem © 2011 Pearson Education, Inc. • Monocots and eudicots differ in the arrangement of veins, the vascular tissue of leaves – Most monocots have parallel veins – Most eudicots have branching veins • In classifying angiosperms, taxonomists may use leaf morphology as a criterion © 2011 Pearson Education, Inc. Figure 35.6 Simple leaf Axillary bud Compound leaf Leaflet Petiole Doubly compound leaf Petiole Axillary bud Petiole Axillary bud Leaflet • Some plant species have evolved modified leaves that serve various functions © 2011 Pearson Education, Inc. Figure 35.7a Tendrils Figure 35.7b Spines Figure 35.7c Storage leaves Figure 35.7d Reproductive leaves Figure 35.7e Bracts Figure 35.7 Tendrils Spines Storage leaves Reproductive leaves Bracts Dermal, Vascular, and Ground Tissues • Each plant organ has dermal, vascular, and ground tissues • Each of these three categories forms a tissue system • Each tissue system is continuous throughout the plant © 2011 Pearson Education, Inc. Figure 35.8 Dermal tissue Ground tissue Vascular tissue • In nonwoody plants, the dermal tissue system consists of the epidermis • A waxy coating called the cuticle helps prevent water loss from the epidermis • In woody plants, protective tissues called periderm replace the epidermis in older regions of stems and roots • Trichomes are outgrowths of the shoot epidermis and can help with insect defense © 2011 Pearson Education, Inc. Figure 35.9 EXPERIMENT Very hairy pod (10 trichomes/ mm2) Slightly hairy pod (2 trichomes/ mm2) Bald pod (no trichomes) Slightly hairy pod: 25% damage Bald pod: 40% damage RESULTS Very hairy pod: 10% damage • The vascular tissue system carries out longdistance transport of materials between roots and shoots • The two vascular tissues are xylem and phloem • Xylem conveys water and dissolved minerals upward from roots into the shoots • Phloem transports organic nutrients from where they are made to where they are needed © 2011 Pearson Education, Inc. • Tissues that are neither dermal nor vascular are the ground tissue system • Ground tissue internal to the vascular tissue is pith; ground tissue external to the vascular tissue is cortex • Ground tissue includes cells specialized for storage, photosynthesis, and support © 2011 Pearson Education, Inc. • The major types of plant cells are: – – – – – Parenchyma Collenchyma Sclerenchyma Water-conducting cells of the xylem Sugar-conducting cells of the phloem © 2011 Pearson Education, Inc. Parenchyma Cells • Mature parenchyma cells – – – – – Have thin and flexible primary walls Lack secondary walls Are the least specialized Perform the most metabolic functions Retain the ability to divide and differentiate © 2011 Pearson Education, Inc. Figure 35.10a Parenchyma cells in Elodea leaf, with chloroplasts (LM) 60 m Collenchyma Cells • Collenchyma cells are grouped in strands and help support young parts of the plant shoot • They have thicker and uneven cell walls • They lack secondary walls • These cells provide flexible support without restraining growth © 2011 Pearson Education, Inc. Figure 35.10b Collenchyma cells (in Helianthus stem) (LM) 5 m Sclerenchyma Cells • Sclerenchyma cells are rigid because of thick secondary walls strengthened with lignin • They are dead at functional maturity • There are two types: – Sclereids are short and irregular in shape and have thick lignified secondary walls – Fibers are long and slender and arranged in threads © 2011 Pearson Education, Inc. Figure 35.10c 5 m Sclereid cells in pear (LM) 25 m Cell wall Fiber cells (cross section from ash tree) (LM) Water-Conducting Cells of the Xylem • The two types of water-conducting cells, tracheids and vessel elements, are dead at maturity • Tracheids are found in the xylem of all vascular plants © 2011 Pearson Education, Inc. • Vessel elements are common to most angiosperms and a few gymnosperms • Vessel elements align end to end to form long micropipes called vessels © 2011 Pearson Education, Inc. Figure 35.10d Vessel Tracheids 100 m Tracheids and vessels (colorized SEM) Pits Perforation plate Vessel element Vessel elements, with perforated end walls Tracheids Sugar-Conducting Cells of the Phloem • Sieve-tube elements are alive at functional maturity, though they lack organelles • Sieve plates are the porous end walls that allow fluid to flow between cells along the sieve tube • Each sieve-tube element has a companion cell whose nucleus and ribosomes serve both cells © 2011 Pearson Education, Inc. Figure 35.10e 3 m Sieve-tube elements: longitudinal view (LM) Sieve plate Sieve-tube element (left) Companion and companion cell: cells cross section (TEM) Sieve-tube elements Plasmodesma Sieve plate 30 m Nucleus of companion cell 15 m Sieve-tube elements: longitudinal view Sieve plate with pores (LM) Figure 35.10eb Sieve-tube elements: longitudinal view (LM) Sieve plate Companion cells Sieve-tube elements 30 m Figure 35.10ed Sieve-tube elements Plasmodesma Sieve plate Nucleus of companion cell Sieve-tube elements: longitudinal view Figure 35.10ec Sieve plate 15 m Sieve plate with pores (LM) Concept 35.2: Meristems generate cells for primary and secondary growth • A plant can grow throughout its life; this is called indeterminate growth • Some plant organs cease to grow at a certain size; this is called determinate growth © 2011 Pearson Education, Inc. • Meristems are perpetually embryonic tissue and allow for indeterminate growth • Apical meristems are located at the tips of roots and shoots and at the axillary buds of shoots • Apical meristems elongate shoots and roots, a process called primary growth © 2011 Pearson Education, Inc. • Lateral meristems add thickness to woody plants, a process called secondary growth • There are two lateral meristems: the vascular cambium and the cork cambium • The vascular cambium adds layers of vascular tissue called secondary xylem (wood) and secondary phloem • The cork cambium replaces the epidermis with periderm, which is thicker and tougher © 2011 Pearson Education, Inc. Figure 35.11 Primary growth in stems Epidermis Cortex Primary phloem Shoot tip (shoot apical meristem and young leaves) Axillary bud meristem Primary xylem Pith Vascular cambium Secondary growth in stems Lateral Cork meristems cambium Cork cambium Periderm Cortex Primary phloem Secondary phloem Pith Root apical meristems Primary xylem Secondary xylem Vascular cambium • Meristems give rise to: – Initials, also called stem cells, which remain in the meristem – Derivatives, which become specialized in mature tissues • In woody plants, primary growth and secondary growth occur simultaneously but in different locations © 2011 Pearson Education, Inc. Figure 35.12 Apical bud Bud scale Axillary buds This year’s growth (one year old) Leaf scar Bud scar Node Internode Last year’s growth (two year old) Leaf scar Stem Bud scar Growth of two years ago (three years old) Leaf scar One-year-old side branch formed from axillary bud near shoot tip • Flowering plants can be categorized based on the length of their life cycle – Annuals complete their life cycle in a year or less – Biennials require two growing seasons – Perennials live for many years © 2011 Pearson Education, Inc. Concept 35.3: Primary growth lengthens roots and shoots • Primary growth produces the parts of the root and shoot systems produced by apical meristems © 2011 Pearson Education, Inc. Primary Growth of Roots • The root tip is covered by a root cap, which protects the apical meristem as the root pushes through soil • Growth occurs just behind the root tip, in three zones of cells: – Zone of cell division – Zone of elongation – Zone of differentiation, or maturation © 2011 Pearson Education, Inc. Figure 35.13 Cortex Vascular cylinder Epidermis Root hair Zone of differentiation Key to labels Dermal Ground Vascular Zone of elongation Zone of cell division (including apical meristem) Root cap Mitotic cells 100 m Figure 35.13a Mitotic cells 100 m • The primary growth of roots produces the epidermis, ground tissue, and vascular tissue • In angiosperm roots, the stele is a vascular cylinder • In most eudicots, the xylem is starlike in appearance with phloem between the “arms” • In many monocots, a core of parenchyma cells is surrounded by rings of xylem then phloem © 2011 Pearson Education, Inc. Figure 35.14 Primary Growth of Roots Epidermis Cortex Endodermis Vascular cylinder 100 m (a) Root with xylem and phloem in the center (typical of eudicots) 50 m Pericycle Core of parenchyma cells Xylem Phloem Endodermis Pericycle Xylem Phloem 100 m (b) Root with parenchyma in the center (typical of monocots) Key to labels Dermal Ground Vascular Figure 35.14aa Primary Growth of Roots Epidermis Cortex Endodermis Vascular cylinder Key to labels Dermal Ground Vascular Pericycle Xylem Phloem 100 m (a) Root with xylem and phloem in the center (typical of eudicots) Figure 35.14b Epidermis Cortex Primary Growth of Roots Key to labels Dermal Endodermis Ground Vascular Vascular cylinder Pericycle Core of parenchyma cells Xylem Phloem 100 m (b) Root with parenchyma in the center (typical of monocots) Figure 35.15-1 Emerging lateral root 100 m Cortex Vascular cylinder 1 Pericycle Figure 35.15-2 Emerging lateral root 100 m Epidermis Lateral root Cortex Vascular cylinder 1 Pericycle 2 Figure 35.15-3 Emerging lateral root 100 m Epidermis Lateral root Cortex Vascular cylinder 1 Pericycle 2 3 Figure 35.17 Tissue Organization of Stems Phloem Xylem Sclerenchyma (fiber cells) Pith Epidermis Cortex Vascular bundle Ground tissue Ground tissue connecting pith to cortex 1 mm (a) Cross section of stem with vascular bundles forming a ring (typical of eudicots) Epidermis Key to labels Vascular bundles Dermal 1 mm Ground Vascular (b) Cross section of stem with scattered vascular bundles (typical of monocots) Tissue Organization of Leaves • The epidermis in leaves is interrupted by stomata, which allow CO2 and O2 exchange between the air and the photosynthetic cells in a leaf • Each stomatal pore is flanked by two guard cells, which regulate its opening and closing • The ground tissue in a leaf, called mesophyll, is sandwiched between the upper and lower epidermis © 2011 Pearson Education, Inc. • The mesophyll of eudicots has two layers: – The palisade mesophyll in the upper part of the leaf – The spongy mesophyll in the lower part of the leaf; the loose arrangement allows for gas exchange © 2011 Pearson Education, Inc. • The vascular tissue of each leaf is continuous with the vascular tissue of the stem • Veins are the leaf’s vascular bundles and function as the leaf’s skeleton • Each vein in a leaf is enclosed by a protective bundle sheath © 2011 Pearson Education, Inc. Figure 35.18 Dermal Stomatal pore Ground Epidermal cell Vascular Sclerenchyma fibers Cuticle Stoma Upper epidermis Palisade mesophyll 50 m Guard cells Key to labels (b) Surface view of a spiderwort (Tradescantia) leaf (LM) 100 m Spongy mesophyll Lower epidermis Xylem Vein Cuticle Guard cells Phloem Guard Vein Air spaces cells (c) Cross section of a lilac (a) Cutaway drawing of leaf tissues (Syringa) leaf (LM) Bundlesheath cell Figure 35.18a Key to labels Sclerenchyma fibers Cuticle Dermal Stoma Ground Vascular Upper epidermis Palisade mesophyll Spongy mesophyll Bundlesheath cell Lower epidermis Xylem Vein Phloem (a) Cutaway drawing of leaf tissues Guard cells Cuticle Figure 35.18b Stomatal pore Epidermal cell 50 m Guard cells (b) Surface view of a spiderwort (Tradescantia) leaf (LM) Figure 35.18c Spongy mesophyll Lower epidermis 100 m Upper epidermis Palisade mesophyll Guard cells Vein Air spaces (c) Cross section of a lilac (Syringa) leaf (LM) Concept 35.4: Secondary growth increases the diameter of stems and roots in woody plants • Secondary growth occurs in stems and roots of woody plants but rarely in leaves • The secondary plant body consists of the tissues produced by the vascular cambium and cork cambium • Secondary growth is characteristic of gymnosperms and many eudicots, but not monocots © 2011 Pearson Education, Inc. Figure 35.19a-1 (a) Primary and secondary growth in a two-year-old woody stem Epidermis Cortex Primary phloem Vascular cambium Primary xylem Pith Periderm (mainly cork cambia and cork) Secondary phloem Secondary xylem Pith Primary xylem Vascular cambium Primary phloem Cortex Epidermis Figure 35.19a-2 (a) Primary and secondary growth in a two-year-old woody stem Epidermis Cortex Primary phloem Vascular cambium Primary xylem Pith Pith Primary xylem Vascular cambium Primary phloem Cortex Epidermis Vascular ray Secondary xylem Secondary phloem First cork cambium Cork Periderm (mainly cork cambia and cork) Secondary phloem Secondary xylem Figure 35.19a-3 (a) Primary and secondary growth in a two-year-old woody stem Epidermis Cortex Primary phloem Vascular cambium Primary xylem Pith Pith Primary xylem Vascular cambium Primary phloem Cortex Epidermis Vascular ray Secondary xylem Secondary phloem First cork cambium Cork Periderm (mainly cork cambia and cork) Secondary phloem Secondary xylem Most recent cork cambium Cork Bark Layers of periderm Figure 35.19b Secondary xylem Secondary phloem Vascular cambium Late wood Early wood Bark Cork cambium 0.5 mm Cork Vascular ray 0.5 mm Growth ring (b) Cross section of a three-yearold Tilia (linden) stem (LM) Periderm Figure 35.20 Vascular cambium Growth Secondary xylem After one year of growth Vascular cambium Secondary phloem After two years of growth Figure 35.22 Growth ring Vascular ray Heartwood Secondary xylem Sapwood Vascular cambium Secondary phloem Bark Layers of periderm Figure 35.23 The Cork Cambium and the Production of Periderm • Cork cambium gives rise to two tissues: – Phelloderm is a thin layer of parenchyma cells that forms to the interior of the cork cambium – Cork cells accumulate to the exterior of the cork cambium • Cork cells deposit waxy suberin in their walls, then die • Periderm consists of the cork cambium, phelloderm, and cork cells it produces © 2011 Pearson Education, Inc. • Lenticels in the periderm allow for gas exchange between living stem or root cells and the outside air • Bark consists of all the tissues external to the vascular cambium, including secondary phloem and periderm © 2011 Pearson Education, Inc. Evolution of Secondary Growth • In the herbaceous plant Arabidopsis, the addition of weights to the plants triggered secondary growth • This suggests that stem weight is the cue for wood formation © 2011 Pearson Education, Inc. Concept 35.5: Growth, morphogenesis, and cell differentiation produce the plant body • Cells form specialized tissues, organs, and organisms through the process of development • Developmental plasticity describes the effect of environment on development – For example, the aquatic plant fanwort forms different leaves depending on whether or not the apical meristem is submerged © 2011 Pearson Education, Inc. Figure 35.24 • Development consists of growth, morphogenesis, and cell differentiation • Growth is an irreversible increase in size • Morphogenesis is the development of body form and organization • Cell differentiation is the process by which cells with the same genes become different from each other © 2011 Pearson Education, Inc. Model Organisms: Revolutionizing the Study of Plants • New techniques and model organisms are catalyzing explosive progress in our understanding of plants • Arabidopsis is a model organism and the first plant to have its entire genome sequenced • Arabidopsis has 27,000 genes divided among 5 pairs of chromosomes © 2011 Pearson Education, Inc. • Arabidopsis is easily transformed by introducing foreign DNA via genetically altered bacteria • Studying the genes and biochemical pathways of Arabidopsis will provide insights into plant development, a major goal of systems biology © 2011 Pearson Education, Inc. Figure 35.28 Orientation of Cell Expansion • Plant cells grow rapidly and “cheaply” by intake and storage of water in vacuoles • Plant cells expand primarily along the plant’s main axis • Cellulose microfibrils in the cell wall restrict the direction of cell elongation © 2011 Pearson Education, Inc. Figure 35.29 Cellulose microfibrils Elongation Nucleus Vacuoles 5 m Morphogenesis and Pattern Formation • Pattern formation is the development of specific structures in specific locations • Two types of hypotheses explain the fate of plant cells – Lineage-based mechanisms propose that cell fate is determined early in development and passed on to daughter cells – Position-based mechanisms propose that cell fate is determined by final position © 2011 Pearson Education, Inc. • Hox genes in animals affect the number and placement of appendages in embryos • A plant homolog of Hox genes called KNOTTED-1 does not affect the number or placement of plant organs • KNOTTED-1 is important in the development of leaf morphology © 2011 Pearson Education, Inc. Figure 35.30 Genetic Control of Flowering • Flower formation involves a phase change from vegetative growth to reproductive growth • It is triggered by a combination of environmental cues and internal signals • Transition from vegetative growth to flowering is associated with the switching on of floral meristem identity genes © 2011 Pearson Education, Inc. • In a developing flower, the order of each primordium’s emergence determines its fate: sepal, petal, stamen, or carpel • Plant biologists have identified several organ identity genes (plant homeotic genes) that regulate the development of floral pattern • These are MADS-box genes • A mutation in a plant organ identity gene can cause abnormal floral development © 2011 Pearson Education, Inc. Figure 35.33 Pe Ca St Se Pe Se (a) Normal Arabidopsis flower Pe Pe Se (b) Abnormal Arabidopsis flower • Researchers have identified three classes of floral organ identity genes • The ABC hypothesis of flower formation identifies how floral organ identity genes direct the formation of the four types of floral organs • An understanding of mutants of the organ identity genes depicts how this model accounts for floral phenotypes © 2011 Pearson Education, Inc. Figure 35.34 Sepals Petals Stamens A B (a) A schematic diagram of the ABC hypothesis Carpels C AB gene activity BC gene activity C gene activity Carpel Petal A gene activity Stamen Sepal Active genes: B B BB A A CCCC A A B B B B C C CCCC C C AA C C C C A A A A AA AB BA AB B A Mutant lacking A Mutant lacking B Mutant lacking C Whorls: Carpel Petal Stamen Sepal Wild type (b) Side view of flowers with organ identity mutations Figure 35.34a Sepals (a) A schematic diagram of the ABC hypothesis Petals Stamens A B Carpels C AB gene activity BC gene activity C gene activity Carpel Petal A gene activity Stamen Sepal Figure 35.34b Active genes: B B B B A ACCCC AA BB BB CCCCCCCC A A C CC C A A A A A A ABBAAB B A Mutant lacking A Mutant lacking B Mutant lacking C Whorls: Carpel Stamen Petal Sepal Wild type (b) Side view of flowers with organ identity mutations