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9780471738435

Esau's Plant Anatomy Meristems, Cells, and Tissues of the Plant Body: Their Structure, Function, and Development

by ;
  • ISBN13:

    9780471738435

  • ISBN10:

    0471738433

  • Edition: 3rd
  • Format: Hardcover
  • Copyright: 2006-09-12
  • Publisher: Wiley-Liss

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Summary

This revision of the now classic Esau's Plant Anatomy offers a completely updated review of the structure, function, and development of meristems, cells, and tissues of the plant body. The text follows a logical structure-based organization. Beginning with a general overview, chapters then cover the protoplast, cell wall, and meristems, through to phloem, periderm, and secretory structures.

Author Biography

Ray F. Evert, Ph.D. is Professor of Botany and Plant Pathology at the University of Wisconsin, Madison.

Table of Contents

Preface xv
Acknowledgments xvii
General References xix
Structure and Development of the Plant Body---An Overview
1(14)
Internal Organization of the Plant Body
3(3)
The Body of a Vascular Plant Is Composed of Three Tissue Systems
3(1)
Structurally Stem, Leaf, and Root Differ Primarily in the Relative Distribution of the Vascular and Ground Tissues
3(3)
Summary of Types of Cells and Tissues
6(1)
Development of the Plant Body
7(5)
The Body Plan of the Plant Is Established during Embryogenesis
7(4)
With Germination of the Seed, the Embryo Resumes Growth and Gradually Develops into an Adult Plant
11(1)
References
12(3)
The Protoplast: Plasma Membrane, Nucleus, and Cytoplasmic Organelles
15(30)
Prokaryotic and Eukaryotic Cells
16(1)
Cytoplasm
17(2)
Plasma Membrane
19(3)
Nucleus
22(1)
Cell Cycle
23(2)
Plastids
25(6)
Chloroplasts Contain Chlorophyll and Carotenoid Pigments
25(1)
Chromoplasts Contain Only Carotenoid Pigments
26(2)
Leucoplasts Are Nonpigmented Plastids
28(1)
All Plastids Are Derived Initially from Proplastids
28(3)
Mitochondria
31(2)
Peroxisomes
33(1)
Vacuoles
34(2)
Ribosomes
36(1)
References
37(8)
The Protoplast: Endomembrane System, Secretory Pathways, Cytoskeleton, and Stored Compounds
45(20)
Endomembrane System
45(4)
The Endoplasmic Reticulum Is a Continuous, Three-dimensional Membrane System That Permeates the Entire Cytosol
45(3)
The Golgi Apparatus Is a Highly Polarized Membrane System Involved in Secretion
48(1)
Cytoskeleton
49(1)
Microtubules Are Cylindrical Structures Composed of Tubulin Subunits
49(3)
Actin Filaments Consist of Two Linear Chains of Actin Molecules in the Form of a Helix
50(2)
Stored Compounds
52(1)
Starch Develops in the Form of Grains in Plastids
52(6)
The Site of Protein Body Assembly Depends on Protein Composition
53(1)
Oil Bodies Bud from Smooth ER Membranes by an Oleosin-mediated Process
54(1)
Tannins Typically Occur in Vacuoles but Also Are Found in Cell Walls
55(1)
Crystals of Calcium Oxalate Usually Develop in Vacuoles but Also Are Found in the Cell Wall and Cuticle
56(2)
Silica Most Commonly Is Deposited in Cell Walls
58(1)
References
58(7)
Cell Wall
65(38)
Macromolecular Components of the Cell Wall
66(5)
Cellulose Is the Principal Component of Plant Cell Walls
66(1)
The Cellulose Microfibrils Are Embedded in a Matrix of Noncellulosic Molecules
67(1)
Principal Hemicelluoses
67(1)
Pectins
68(1)
Proteins
68(1)
Callose Is a Widely Distributed Cell Wall Polysaccharide
69(1)
Lignins Are Phenolic Polymers Deposited Mainly in Cell Walls of Supporting and Conducting Tissues
69(2)
Cutin and Suberin Are Insoluble Lipid Polymers Found Most Commonly in the Protective Surface Tissues of the Plant
71(1)
Cell Wall Layers
71(3)
The Middle Lamella Frequently Is Difficult to Distinguish from the Primary Wall
72(1)
The Primary Wall Is Deposited While the Cell Is Increasing in Size
72(1)
The Secondary Wall Is Deposited inside the Primary Wall Largely, If Not Entirely, after the Primary Wall Has Stopped Increasing in Surface Area
72(2)
Pits and Primary Pit-Fields
74(2)
Origin of Cell Wall during Cell Division
76(4)
Cytokinesis Occurs by the Formation of a Phragmoplast and Cell Plate
76(2)
Initially Callose Is the Principal Cell Wall Polysaccharide Present in the Developing Cell Plate
78(1)
The Preprophase Band Predicts the Plane of the Future Cell Plate
78(2)
Growth of the Cell Wall
80(3)
The Orientation of Cellulose Microfibrils within the Primary Wall Influences the Direction of Cell Expansion
82(1)
When Considering the Mechanism of Wall Growth, It Is Necessary to Distinguish between Growth in Surface (Wall Expansion) and Growth in Thickness
83(1)
Expansion of the Primary Cell Wall
83(1)
Cessation of Wall Expansion
84(1)
Intercellular Spaces
84(1)
Plasmodesmata
85(6)
Plasmodesmata May Be Classified as Primary or Secondary According to Their Origin
85(2)
Plasmodesmata Contain Two Types of Membranes: Plasma Membrane and Desmotubule
87(1)
Plasmodesmata Enable Cells to Communicate
88(2)
The Symplast Undergoes Reorganization throughout the Course of Plant Growth and Development
90(1)
References
91(12)
Meristems and Differentiation
103(30)
Meristems
103(7)
Classification of Meristems
104(1)
A Common Classification of Meristems Is Based on Their Position in the Plant Body
104(2)
Meristems Are Also Classified According to the Nature of Cells That Give Origin to Their Initial Cells
106(1)
Characteristics of Meristematic Cells
106(1)
Growth Patterns in Meristems
107(1)
Meristematic Activity and Plant Growth
108(2)
Differentiation
110(5)
Terms and Concepts
110(1)
Senescence (Programmed Cell Death)
111(2)
Cellular Changes in Differentiation
113(1)
A Cytologic Phenomenon Commonly Observed in Differentiating Cells of Angiosperms Is Endopolyploidy
113(1)
One of the Early Visible Changes in Differentiating Tissues Is the Unequal Increase in Cell Size
113(1)
Intercellular Adjustment in Differentiating Tissue Involves Coordinated and Intrusive Growth
114(1)
Causal Factors in Differentiation
115(5)
Tissue Culture Techniques Have Been Useful for the Determination of Requirements for Growth and Differentiation
115(2)
The Analysis of Genetic Mosaics Can Reveal Patterns of Cell Division and Cell Fate in Developing Plants
117(1)
Gene Technologies Have Dramatically Increased Our Understanding of Plant Development
117(2)
Polarity Is a Key Component of Biological Pattern Formation and Is Related to the Phenomenon of Gradients
119(1)
Plant Cells Differentiate According to Position
119(1)
Plant Hormones
120(3)
Auxins
121(1)
Cytokinins
122(1)
Ethylene
123(1)
Abscisic Acid
123(1)
Gibberellins
123(1)
References
123(10)
Apical Meristems
133(42)
Evolution of the Concept of Apical Organization
134(2)
Apical Meristems Originally Were Envisioned as Having a Single Initial Cell
134(1)
The Apical-Cell Theory Was Superseded by the Histogen Theory
134(1)
The Tunica-Corpus Concept of Apical Organization Applies Largely to Angiosperms
135(1)
The Shoot Apices of Most Gymnosperms and Angiosperms Show a Cytohistological Zonation
136(1)
Inquiries into the Identity of Apical Initials
136(2)
Vegetative Shoot Apex
138(5)
The Presence of an Apical Cell Is Characteristic of Shoot Apices in Seedless Vascular Plants
139(1)
The Zonation Found in the Ginkgo Apex Has Served as a Basis for the Interpretation of Shoot Apices in Other Gymnosperms
140(1)
The Presence of a Zonation Superimposed on a Tunica-Corpus Configuration Is Characteristic of Angiosperm Shoot Apices
141(2)
The Vegetative Shoot Apex of Arabidopsis thaliana
143(2)
Origin of Leaves
145(4)
Throughout the Vegetative Period the Shoot Apical Meristem Produces Leaves in a Regular Order
145(2)
The Initiation of a Leaf Primordium Is Associated with an Increase in the Frequency of Periclinal Divisions at the Initiation Site
147(2)
Leaf Primordia Arise at Sites That Are Correlated with the Phyllotaxis of the Shoot
149(1)
Origin of Branches
149(3)
In Most Seed Plants Axillary Meristems Originate from Detached Meristems
150(2)
Shoots May Develop from Adventitious Buds
152(1)
Root Apex
152(8)
Apical Organization in Roots May Be either Open or Closed
153(4)
The Quiescent Center Is Not Completely Devoid of Divisions under Normal Conditions
157(3)
The Root Apex of Arabidopsis thaliana
160(2)
Growth of the Root Tip
162(3)
References
165(10)
Parenchyma and Collenchyma
175(16)
Parenchyma
175(7)
Parenchyma Cells May Occur in Continuous Masses as Parenchyma Tissue or Be Associated with Other Cell Types in Morphologically Heterogeneous Tissues
176(1)
The Contents of Parenchyma Cells Are a Reflection of the Activities of the Cells
177(1)
The Cell Walls of Parenchyma Cells May Be Thick or Thin
178(1)
Some Parenchyma Cells---Transfer Cells---Contain Wall Ingrowths
179(2)
Parenchyma Cells Vary Greatly in Shape and Arrangement
181(1)
Some Parenchyma Tissue---Aerenchyma---Contains Particularly Large Intercellular Spaces
182(1)
Collenchyma
183(4)
The Structure of the Cell Walls of Collenchyma Is the Most Distinctive Characteristic of This Tissue
184(1)
Collenchyma Characteristically Occurs in a Peripheral Position
185(2)
Collenchyma Appears to Be Particularly Well Adapted for Support of Growing Leaves and Stems
187(1)
References
187(4)
Sclerenchyma
191(20)
Fibers
192(6)
Fibers Are Widely Distributed in the Plant Body
192(2)
Fibers May Be Divided into Two Large Groups, Xylary and Extraxylary
194(2)
Both Xylary and Extraxylary Fibers May Be Septate or Gelatinous
196(1)
Commercial Fibers Are Separated into Soft Fibers and Hard Fibers
197(1)
Sclereids
198(4)
Based on Shape and Size, Sclereids May Be Classified into a Number of Types
198(1)
Sclereids Like Fibers Are Widely Distributed in the Plant Body
199(1)
Sclereids in Stems
200(1)
Sclereids in Leaves
200(1)
Sclereids in Fruits
201(1)
Sclereids in Seeds
201(1)
Origin and Development of Fibers and Sclereids
202(3)
Factors Controlling Development of Fibers and Sclereids
205(2)
References
207(4)
Epidermis
211(44)
Ordinary Epidermal Cells
214(4)
Epidermal Cell Walls Vary in Thickness
214(1)
The Most Distinctive Feature of the Outer Epidermal Wall Is the Presence of a Cuticle
215(3)
Stomata
218(11)
Stomata Occur on All Aerial Parts of the Primary Plant Body
218(3)
Guard Cells Are Generally Kidney-shaped
221(1)
Guard Cells Typically Have Unevenly Thickened Walls with Radially Arranged Cellulose Microfibrils
222(2)
Blue Light and Abscisic Acid Are Important Signals in the Control of Stomatal Movement
224(1)
Development of Stomatal Complexes Involves One or More Asymmetric Cell Divisions
225(3)
Different Developmental Sequences Result in Different Configurations of Stomatal Complexes
228(1)
Trichomes
229(8)
Trichomes Have a Variety of Functions
229(1)
Trichomes May Be Classified into Different Morphological Categories
230(1)
A Trichome Is Initiated as a Protuberance from an Epidermal Cell
230(1)
The Cotton Fiber
230(4)
Root Hairs
234(1)
The Arabidopsis Trichome
235(2)
Cell Patterning in the Epidermis
237(2)
The Spatial Distribution of Stomata and Trichomes in Leaves Is Nonrandom
237(1)
There Are Three Main Types of Patterning in the Epidermis of Angiosperm Roots
238(1)
Other Specialized Epidermal Cells
239(4)
Silica and Cork Cells Frequently Occur Together in Pairs
239(2)
Bulliform Cells Are Highly Vacuolated Cells
241(1)
Some Epidermal Hairs Contain Cystoliths
242(1)
References
243(12)
Xylem: Cell Types and Developmental Aspects
255(36)
Cell Types of the Xylem
256(12)
Tracheary Elements---Tracheids and Vessel Elements---Are the Conducting Cells of the Xylem
256(4)
The Secondary Walls of Most Tracheary Elements Contain Pits
260(3)
Vessels Are More Efficient Conduits of Water Than Are Tracheids
263(3)
Fibers Are Specialized as Supporting Elements in the Xylem
266(1)
Living Parenchyma Cells Occur in Both the Primary and Secondary Xylem
266(1)
In Some Species the Parenchyma Cells Develop Protrusions---Tyloses---That Enter the Vessels
267(1)
Phylogenetic Specialization of Tracheary Elements and Fibers
268(3)
The Major Trends in the Evolution of the Vessel Element Are Correlated with Decrease in Vessel Element Length
268(2)
Deviations Exist in Trends of Vessel Element Evolution
270(1)
Like Vessel Elements and Tracheids, Fibers Have Undergone a Phylogenetic Shortening
271(1)
Primary Xylem
271(5)
Some Developmental and Structural Differences Exist between the Earlier and Later Formed Parts of the Primary Xylem
271(2)
The Primary Tracheary Elements Have a Variety of Secondary Wall Thickenings
273(3)
Tracheary Element Differentiation
276(7)
Plant Hormones Are Involved in the Differentiation of Tracheary Elements
280(1)
Isolated Mesophyll Cells in Culture Can Transdifferentiate Directly into Tracheary Elements
281(2)
References
283(8)
Xylem: Secondary Xylem and Variations in Wood Structure
291(32)
Basic Structure of Secondary Xylem
293(9)
The Secondary Xylem Consists of Two Distinct Systems of Cells, Axial and Radial
293(1)
Some Woods Are Storied and Others Are Nonstoried
294(1)
Growth Rings Result from the Periodic Activity of the Vascular Cambium
294(3)
As Wood Becomes Older, It Gradually Becomes Nonfunctional in Conduction and Storage
297(2)
Reaction Wood Is a Type of Wood That Develops in Branches and Learning or Crooked Stems
299(3)
Woods
302(10)
The Wood of Conifers Is Relatively Simple in Structure
302(1)
The Axial System of Conifer Woods Consists Mostly or Entirely of Tracheids
302(1)
The Rays of Conifers May Consist of Both Parenchyma Cells and Tracheids
303(1)
The Wood of Many Conifers Contains Resin Ducts
304(2)
The Wood of Angiosperms Is More Complex and Varied Than That of Conifers
306(1)
On the Basis of Porosity, Two Main Types of Angiosperm Wood Are Recognized: Diffuse-porous and Ring-porous
307(2)
The Distribution of Axial Parenchyma Shows Many Intergrading Patterns
309(1)
The Rays of Angiosperms Typically Contain Only Parenchyma Cells
310(2)
Intercellular Spaces Similar to the Resin Ducts of Gymnosperms Occur in Angiosperm Woods
312(1)
Some Aspects of Secondary Xylem Development
312(3)
Identification of Wood
315(1)
References
316(7)
Vascular Cambium
323(34)
Organization of the Cambium
323(3)
The Vascular Cambium Contains Two Types of Initials: Fusiform Initials and Ray Initials
323(2)
The Cambium May Be Storied or Nonstoried
325(1)
Formation of Secondary Xylem and Secondary Phloem
326(1)
Initials Versus Their Immediate Derivatives
327(3)
Developmental Changes
330(6)
Formation of New Ray Initials from Fusiform Initials or Their Segments Is a Common Phenomenon
332(3)
Domains Can Be Recognized within the Cambium
335(1)
Seasonal Changes in Cambial Cell Ultrastructure
336(2)
Cytokinesis of Fusiform Cells
338(3)
Seasonal Activity
341(5)
The Size of the Xylem Increment Produced during One Year Generally Exceeds That of the Phloem
343(1)
A Distinct Seasonality in Cambial Activity Also Occurs in Many Tropical Regions
344(2)
Causal Relations in Cambial Activity
346(2)
References
348(9)
Phloem: Cell Types and Developmental Aspects
357(50)
Cell Types of the Phloem
359(1)
The Angiospermous Sieve-Tube Element
360(12)
In Some Taxa the Sieve-Tube Element Walls Are Remarkably Thick
361(3)
Sieve Plates Usually Occur on End Walls
364(1)
Callose Apparently Plays a Role in Sieve-Pore Development
364(1)
Changes in the Appearance of the Plastids and the Appearance of P-protein Are Early Indicators of Sieve-Tube Element Development
365(7)
Nuclear Degeneration May Be Chromatolytic or Pycnotic
372(1)
Companion Cells
372(7)
The Mechanism of Phloem Transport in Angiosperms
379(3)
The Source Leaf and Minor Vein Phloem
382(4)
Several Types of Minor Veins Occur in Dicotyledonous Leaves
384(1)
Type 1 Species with Specialized Companion Cells, Termed Intermediary Cells, Are Symplastic Loaders
384(1)
Species with Type 2 Minor Veins Are Apoplastic Loaders
385(1)
The Collection of Photoassimilate by the Minor Veins in Some Leaves May Not Involve an Active Step
385(1)
Some Minor Veins Contain More Than One Kind of Companion Cell
385(1)
The Minor Veins in Leaf Blades of the Poaceae Contain Two Types of Metaphloem Sieve Tubes
386(1)
The Gymnospermous Sieve Cell
386(4)
The Walls of Sieve Cells Are Characterized as Primary
387(1)
Callose Does Not Play a Role in Sieve-Pore Development in Gymnosperms
387(1)
Little Variation Exists in Sieve-Cell Differentiation among Gymnosperms
388(2)
Strasburger Cells
390(1)
The Mechanism of Phloem Transport in Gymnosperms
390(1)
Parenchyma Cells
391(1)
Sclerenchyma Cells
391(1)
Longevity of Sieve Elements
391(1)
Trends in Specialization of Sieve-Tube Elements
392(1)
Sieve Elements of Seedless Vascular Plants
393(1)
Primary Phloem
393(5)
References
398(9)
Phloem: Secondary Phloem and Variations in Its Structure
407(20)
Conifer Phloem
409(3)
Angiosperm Phloem
412(5)
The Patterns Formed by the Fibers Can Be of Taxonomic Significance
413(2)
Secondary Sieve-Tube Elements Show Considerable Variation in Form and Distribution
415(2)
Differentiation in the Secondary Phloem
417(5)
Sclerenchyma Cells in the Secondary Phloem Commonly Are Classified as Fibers, Sclereids, and Fiber-Sclereids
418(2)
The Conducting Phloem Constitutes Only a Small Part of the Inner Bark
420(2)
Nonconducting Phloem
422(2)
The Nonconducting Phloem Differs Structurally from the Conducting Phloem
423(1)
Dilatation Is the Means by Which the Phloem Is Adjusted to the Increase in Circumference of the Axis Resulting from Secondary Growth
423(1)
References
424(3)
Periderm
427(20)
Occurrence
427(2)
Characteristics of the Components
429(4)
The Phellogen Is Relatively Simple in Structure
429(1)
Several Kinds of Phellem Cells May Arise from the Phellogen
429(2)
Considerable Variation Exists in the Width and Composition of Phelloderm
431(2)
Development of Periderm
433(4)
The Sites of Origin of the Phellogen Are Varied
433(1)
The Phellogen Is Initiated by Divisions of Various Kinds of Cells
434(1)
The Time of Appearance of the First and Subsequent Periderms Varies
434(3)
Morphology of Periderm and Rhytidome
437(1)
Polyderm
438(1)
Protective Tissue in Monocotyledons
438(1)
Wound Periderm
438(2)
Lenticels
440(2)
Three Structural Types of Lenticels Are Recognized in Woody Angiosperms
441(1)
The First Lenticels Frequently Appear under Stomata
442(1)
References
442(5)
External Secretory Structures
447(26)
Salt Glands
449(2)
Salt Bladders Secrete Ions into a Large Central Vacuole
449(1)
Other Glands Secrete Salt Directly to the Outside
449(1)
The Two-celled Glands of the Poaceae
449(1)
The Multicellular Glands of Eudicotyledons
450(1)
Hydathodes
451(1)
Nectaries
452(7)
The Nectaries of Lonicera japonica Exude Nectar from Unicellular Trichomes
455(1)
The Nectaries of Abutilon striatum Exude Nectar from Multicellular Trichomes
456(1)
The Nectaries of Vicia faba Exude Nectar via Stomata
456(1)
The Most Common Sugars in Nectar Are Sucrose, Glucose, and Fructose
456(3)
Structures Intermediate between Nectaries and Hydathodes Also Exist
459(1)
Colleters
459(2)
Osmophores
461(1)
Glandular Trichomes Secreting Lipophilic Substances
462(1)
Glandular Trichome Development
463(2)
The Glandular Structures of Carnivorous Plants
465(1)
Stinging Hairs
466(1)
References
466(7)
Internal Secretory Structures
473(30)
Internal Secretory Cells
473(5)
Oil Cells Secrete Their Oils into an Oil Cavity
475(1)
Mucilage Cells Deposit Their Mucilage between the Protoplast and the Cellulosic Cell Wall
476(1)
Tannin Is the Most Conspicuous Inclusion in Numerous Secretory Cells
477(1)
Secretory Cavities and Ducts
478(5)
The Best-Known Secretory Ducts Are the Resin Ducts of Conifers
478(1)
Development of Secretory Cavities Appears to Be Schizogenous
479(2)
Secretory Ducts and Cavities May Arise under the Stimulus of Injury
481(1)
Kino Veins Are a Special Type of Traumatic Duct
482(1)
Laticifers
483(10)
On the Basis of Their Structure, Laticifers Are Grouped in Two Major Classes: Articulated and Nonarticulated
484(2)
Latex Varies in Appearance and in Composition
486(1)
Articulated and Nonarticulated Laticifers Apparently Differ from One Another Cytologically
487(2)
Laticifers Are Widely Distributed in the Plant Body, Reflecting Their Mode of Development
489(1)
Nonarticulated Laticifers
489(2)
Articulated Laticifers
491(2)
The Principal Source of Commercial Rubber Is the Bark of the Para Rubber Tree, Hevea brasiliensis
493(2)
The Function of Laticifers Is Not Clear
495(1)
References
495(8)
Addendum: Other Pertinent References Not Cited in the Text 503(18)
Glossary 521(20)
Author Index 541(26)
Subject Index 567

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