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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
AB
gene
activity
BC
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
AB
gene
activity
BC
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