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A. Flowering Plant Structure (p. 638)
- Structures of flowering plants are well-adapted to varied environments.
- Flowering plants have three vegetative organs: root, stem and leaf. (Figs.
36.1 and 36.2)
B. Roots
- We speak of "a root" but it is more appropriate to call it a root system.
- Root system is the main root plus its lateral (side) branches.
(Fig. 36.2a)
- It is generally equal in size to the shoot system, the part above
ground.
- Root systems have the following functions.
- Roots anchor a plant in soil and give support.
- Roots absorb water and minerals from soil; root hairs are central to this
process.
- Root hair cells are in a zone near root tip.
- Root hairs are numerous to increase absorptive surface of a root.
- Transplanting plants without preserving root hairs damages a plant.
- Water and nutrients absorbed are distributed to rest of the plant.
- Roots produce hormones that must be distributed to the plant
- Perennials "die back" to regrow next season; roots store food. (e.g.,
carrots, sweet potatoes).
C. Stems (p. 639)
- Stem forms main axis of a plant, along with lateral branches. (Fig.
36.2b)
- Stem produces leaves and arrays them to be exposed to as much sun as possible..
- A node occurs where a leaf attaches and internode is region
between nodes; nodes and internodes identify a stem even if it is underground.
- Stem has vascular tissue to transport water and minerals from roots and
sugar from leaves.
- Non-living cells form a continuous pipeline in vascular tissue.
- A cylindrical stem expands in girth and length; trees use woody tissue to
strengthen stems.
- Stems function in storage: cactus stems store water; tubers are horizontal
stems that store nutrients.
D. Leaves
- A foliage leaf is the usual organ of photosynthesis in vascular plants.
(Fig. 36.2c)
- Leaves receive water from roots by way of the stem.
- Broad, thin leaves have maximum surface area to absorb CO2
and collect solar energy.
- A blade is the wide portion of a leaf with most photosynthetic tissue.
- Petiole is a stalk that attaches a leaf blade to stem.
- Leaf axil is upper acute angle between petiole and stem where an
axillary (lateral) bud originates.
- Some leaves protect buds, attach to objects, store food, or capture insects.
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36.2. Monocot Versus Dicot Plants |
A. Criteria for Monocots and Dicots (p. 640)
- Flowering plants are
divided into monocots and dicots based on these traits. (Fig.
36.3)
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Monocots
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Dicots
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a.   Number of cotyledons
in seed
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one
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two
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| b.  Distribution of root xylem
and phloem |
root xylem and phloem
in a ring
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root phloem between arms
of xylem
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| c.  Distribution of vascular
bundles |
scattered in stem
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arranged in a distinct
ring
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| d.  Pattern of leaf
veins |
form a parallel pattern
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form a net pattern
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| e.  Number of flower parts |
in threes and multiples
of fours and fives
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in fours, fives and threes
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| f.   Number of apertures
in pollen |
usually one
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usually three grains
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| 2.   Representative
members: |
grasses, lilies, orchids
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dandelions to oak trees
and palm trees
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- Cotyledons are embryonic seed leaves
providing nutrition before mature leaves begin photosynthesis.
- These traits represent an evolutionary path
dating back to origin of flowering plants.
A. Meristem Produces Tissue (p. 641)
- Plants continually grow due to meristem (embryonic tissue) in stem
and root tips.
- Three types of primary meristem produce three types of specialized
tissue.
- Protoderm is outermost primary meristem giving rise to epidermis.
- Ground meristem is inner meristem producing ground tissue.
- Procambium produces vascular tissue.
- Three specialized tissues are produced.
- Epidermal tissue forms outer protective covering.
- Ground tissue fills the interior.
- Vascular tissue transports water and nutrients and provides support.
B. Epidermal Tissue
- Epidermis is an outer protective covering tissue of plant roots,
leaves, and stems of nonwoody plants.
- It contains closely packed epidermal cells.
- Waxy cuticle covers walls of epidermal cells, minimizing water loss
and protecting against bacteria.
- In roots, certain epidermal cells are modified into root hairs that
increase surface area of the root for absorption of water and minerals and
help to anchor plants. (Fig. 36.4a)
- Different protective hairs are produced by epidermal cells of stems and
leaves.
- Epidermal cells are modified as glands to secrete protective substances.
- On lower epidermis of leaves, special guard cells form microscopic
pores (stomates) and regulate gas exchange between leaf interior and
exterior. (Fig. 36.4b)
- In older woody plants, epidermis of the stem is replaced by cork tissue.
(Fig. 36.4c)
- Cork is outer covering of the bark of trees; composed of dead cork
cells that may be sloughed off.
- Cork cambium is lateral meristem that produces new cork cells.
- As cork cells mature, they encrust with lipid suberin that renders
them waterproof and inert.
- Cork protects a plant and makes it resistant to attack by fungi, bacteria,
and animals.
C. Ground Tissue
- Ground tissue fills the inside of plants with parenchyma, collenchyma
and sclerenchyma cells.
- Parenchyma are least specialized of all plant cell types. (Fig. 36.5a)
- Cells of this type contain plastids (e.g., chloroplasts or colorless storage
plastids).
- They are found in all organs of a plant.
- They divide to form more specialized cells (e.g. roots develop from stem
cuttings in water).
- Collenchyma resemble parenchyma but has thicker primary cell walls.
(Fig. 36.5b)
- Collenchyma cells are uneven in the corners.
- They usually occur as bundles of cells just beneath epidermis.
- They give flexible support to immature regions of plants (e.g. celery
stalk is mostly collenchyma).
- Sclerenchyma cells have thick secondary cell walls. (Fig. 36.5c)
- They are impregnated with lignin that renders walls tough and hard.
- They provide strong support to mature regions of plants.
- Most cells of this type are non-living.
- Sclerenchyma cells form fibers (used in linen and rope) and shorter sclereids
(found in seed coats and nut shells).
D. Vascular Tissue
- Xylem passively conducts water and mineral solutes upward through
a plant from roots to leaves;
- Xylem contains tracheids, vessel elements, and parenchyma cells that store
various substances. (Fig. 36.6)
- Tracheids (Fig. 36.6a)
- Tracheids are hollow, thin, long non-living cells with tapered overlapping
ends.
- Water moves across end and sidewalls because of pits or depressions
in secondary cell wall.
- Vessel Elements
- Vessel elements are hollow non-living cells lacking tapered ends.
- They are larger than tracheids.
- They lack transverse end walls.
- They form a continuous pipeline for water and mineral transport.
- Xylem also contains sclerenchyma cells to add support.
- Phloem is vascular tissue that conducts the organic solutes in plants,
from the leaves to the roots; it contains sieve-tube cells and companion
cells. (Fig. 36.7)
- Sieve-tube cells
- Sieve-tube cells contain cytoplasm but no nucleus.
- They are arranged end to end.
- They have channels in their end walls (thus, the name "sieve-tube"),
through which plasmodesmata extend from one cell to another.
- Companion Cells
- Companion cells are closely connected to sieve-tube cells by numerous
plasmodesmata.
- They are smaller and more generalized than sieve-tube cells.
- They have a nucleus which may control and maintain the function of both
cells.
- They are also thought to be involved in the transport function of phloem.
- Vascular tissue extends from root to leaves as vascular cylinder (roots),
vascular bundles (stem) and leaf veins.
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36.4. Organization of Roots (p. 644) |
A. Dicot Root Tip
- Dicot root tip, site of primary growth, is organized into zones of
cells in various stages of differentiation. (Fig. 36.8a)
- Cells are continuously added to a root cap below and zone of elongation
above by contributions from the zone of cell division.
- Root cap is a protective cover; its cells are replaced constantly
because they are soon ground off.
- Zone of elongation is above a zone of cell division where
cells become longer and more specialized.
- Zone of cell division contains meristematic tissue and adds cells
to root tip and zone of elongation.
- Zone of maturation is above zone of elongation; cells are mature
and differentiated and it has root hairs.
B. Tissues of a Dicot Root (Fig. 36.8a)
- Epidermis is a single layer of thin-walled, rectangular cells.
- Epidermis forms protective outer layer of the root.
- In region of maturation, there are many root hairs.
- Root hairs project as far as 5-8 mm into the soil.
- Cortex is a layer of large, thin-walled, irregularly shaped parenchyma
cells.
- These cells contain starch granules; function in food storage.
- Cells are loosely packed; water and minerals can diffuse through cortex
without entering cells.
- Endodermis is layer of rectangular cells; forms boundary between
cortex and inner vascular cylinder.
- Its cells fit closely together and are bordered on four sides by the Casparian
strip.
- It regulates entrance of minerals into vascular cylinder.
- Casparian strip is impermeable lignin and suberin layer that excludes
water and mineral ions. (Fig. 36.8c)
- The only access to the vascular bundle is through endodermal cells.
- Vascular cylinder is an arrangement of vascular tissues as a cylinder.
(Fig. 36.8b)
- Pericycle is first layer of cells within vascular cylinder
- Its cells have retained capacity to divide.
- It can start development of branch or secondary roots. (Fig. 36.9)
- Vascular tissue forms main portion of a vascular bundle; it is
composed of
- xylem, whose cells are arranged in a star-shaped pattern; and
- phloem, whose cells are located in regions between arms of xylem.
C. Organization of Monocot Roots (Fig. 36.10)
- Monocot roots do not undergo secondary growth.
- Monocot root has a ring of vascular tissue; alternating bundles of xylem
and phloem surround pith.
- Monocot roots also have pericycle, endodermis, cortex, and epidermis.
D. Root Diversity
- Roots have adaptations to help anchor plants, absorb water and minerals,
and store carbohydrates.
- There are three general root types:
- Taproot is common in dicots; first or primary root grows
straight down and remains dominant root of a plant; often fleshy and adapted
to store food (e.g., carrots, beets). (Fig. 36.11a)
- Fibrous root system of monocots is a mass of slender roots and
lateral branches that hold soil. (Fig. 36.11b)
- Adventitious roots develop from underground stems or from base
of above-ground stems.
- Prop roots main function is to anchor a plant (e.g. corn and
mangrove plants). (Fig. 36.11c)
- Pneumatophores of mangrove plants project above the water from
roots to acquire oxygen.
- Ivy has holdfast roots to anchor aerial shoots.
- Haustoria are root-like projections of stems of parasitic plants
(e.g., dodders and broomrapes).
- They grow into the host plant.
- They contact vascular tissue from which they extract water and nutrients.
- Mycorrhizae are fungus roots.
- In this mutualism, fungus receives sugars and amino acids from plant.
- Plant receives water and minerals from the fungus.
- Legumes (e.g., peas and beans) have root nodules containing nitrogen-fixing
bacteria.
- Bacteria extract nitrogen from air and reduce it to a form that can be
used by plant tissues.
- Legumes are often planted to bolster nitrogen supply of soil.
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36.5. Organization of Stems |
A. Primary Growth (p. 648)
- Stem tip is site of primary growth where cell division extends length
of stems or roots.
- Shoot apical meristem produces new leaves and primary meristems;
increases stem length. (Fig. 36.12)
- Shoot apical meristem is protected within a terminal bud of leaf primordia
(immature leaves).
- Bud scales are scale-like coverings protecting terminal buds during
winters when bud growth stops.
- Three specialized types of primary meristem develop from shoot apical meristem.
(Fig. 36.12b)
- Protoderm is outermost primary meristem that gives rise to epidermis.
- Ground meristem produces two tissues composed of parenchyma cells:
pith and cortex.
- Procambium is inner meristem that produces primary xylem
and primary phloem.
- Differentiation continues; cells become first tracheids or vessel elements
within vascular bundle.
- First sieve-tube cells are short-lived and do not have companion cells.
- Mature phloem develops later after all surrounding cells have stopped expanding.
B. Herbaceous Stems
- Herbaceous stems are mature nonwoody stems that exhibit only primary
growth.
- Outermost tissue of herbaceous stems is epidermis covered by waxy cuticle
to prevent water loss. (Fig. 36.13)
- Xylem and phloem are in distinctive vascular bundles.
- In each bundle, xylem is found to inside of stem; phloem is found to outside.
(Fig. 36.13b)
- In dicot herbaceous stem, vascular bundles are arranged in a ring towards
outside of the stem and separating cortex from central pith. (Fig. 36.13a)
- In monocot stem, vascular bundles are scattered throughout the stem; there
is no well-defined cortex or pith. (Fig. 36.14)
- Cortex sometimes carries on photosynthesis; pith may function as a storage
site.
C. Woody Stems (Fig. 36.15)
- Woody plants have both primary and secondary tissues.
- Primary tissues are new and form each year from primary meristem right behind
apical meristem.
- Secondary tissues develop from second year onward from growth of lateral
meristem.
- Primary growth increases length of a plant; secondary growth
increases its girth. (Fig. 36.16)
- As secondary growth continues, it is not possible to distinguish individual
vascular bundles.
- Woody dicot stem has a different organization with three distinct areas:
bark, wood, and pith.
- Rays are of living cells that allow materials to move laterally.
- Bark of a tree contains cork, cork cambium, and phloem.
- Secondary phloem is produced each year by vascular cambium but does not
build up.
- This phloem tissue is soft; therefore it is easy to remove the bark of
a tree..
- Cork cambium is a lateral meristem that produces new cork cells when
needed.
- Cork cambium begins to divide, producing cork that disrupts epidermis
replacing it with cork cells.
- Cork cells become impregnated with suberin, causing them to die but making
them waterproof..
- Consequently, cork forms an impervious barrier, even to gas exchange,
except at lenticels,
- First flowering plants were probably woody shrubs; herbaceous plants evolved
later.
- It is advantageous to be woody when there is adequate rainfall; woody
plants can grow taller and have adequate tissue to support and service leaves.
- It takes energy to support secondary growth and prepare plant for winter
in temperate zones.
- Long-lasting plants need more defense mechanisms against attack by herbivores
and parasites.
- Trees need years to mature before reproducing; they are more vulnerable
to accident or disease.
- Annual Rings
- Vascular cambium is dormant during winter.
- Spring wood is composed of wide xylem vessel elements with thin
walls, necessary to conduct of sufficient water and nutrients to supply
abundant growth that occurs during spring.
- Summer wood forms when moisture is scarce; composed of a lower
proportion of vessels, it contains thick-walled tracheids and numerous fibers.
- Annual ring is one ring of spring wood followed by a ring of summer
wood; equals one year's growth. (Fig. 36.15 and 36A)
- Sapwood is outer annual rings where transport occurs. (Fig. 36.15b,
c)
- Heartwood is inner annual rings of older trees.
- Vessels no longer function in transport; they become plugged with resins
and gums that inhibit growth of bacteria and fungi.
- Heartwood may help to support a tree.
D. Stem Diversity
- Stolons are stems that grow along ground; new plants grow where nodes
contact soil. (Fig. 36.17a)
- Succulent stems of cacti are modified for water storage.
- Tendrils of grapes and morning glories are stems adapted for wrapping around
support structures.
- Rhizomes are underground horizontal stems.
- Rhizomes are long and thin in grasses and thick and fleshy in irises.
(Fig. 36.17b)
- Rhizomes survive winter and contribute to asexual reproduction because
each node bears a bud.
- Some rhizomes have tubers that function in food storage (e.g.,
potatoes). (Fig. 36.17c)
- Corms are bulbous underground stems that lie dormant during winter,
like rhizomes. (Fig. 36.17d)
- Humans use stems: sugarcane is primary source of table sugar; cinnamon and
quinine are from bark.
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36.6. Organization of Leaves (p. 654) |
A. Leaf Structure (Fig. 36.18)
- Leaves are organs of photosynthesis in plants; they are made of a flattened
blade and a petiole.
- Leaf veins reveal the presence of vascular tissue within the leaves.
- The vascular tissues of leaves transport water and nutrients.
- Leaf veins have a net pattern in dicot leaves and a parallel pattern in
monocot leaves. (Fig. 36.3)
- A petiole is a stalk that attaches a leaf blade to the plant stem.
- Epidermis is the layer of cells that covers the top and bottom sides
of a leaf.
- Epidermis often bears protective hairs or glands; epidermal glands produce
irritating substances.
- Epidermis is covered by a waxy cuticle that keeps the leaf from
drying out.
- Epidermis, particularly lower epidermis, contains stomates that
allow gases to move into and out of leaf.
- Mesophyll is the inner body of a leaf and the site of most of photosynthesis.
- Palisade mesophyll is layer of mesophyll containing elongated parenchyma
cells with many chloroplasts.
- Spongy mesophyll contains loosely packed parenchyma cells that
increase surface area for gas exchange.
B. Leaf Diversity (Fig. 36.19)
- Simple leaves have margins not deeply lobed or divided into smaller
leaflets.
- Compound leaves are divided into smaller leaflets, and each leaflet
may have its own stalk.
- Leaves are variously modified.
- Cactus spines are modified leaves; succulents have fleshy leaves to hold
moisture. (Fig. 36.20a)
- Onion bulbs have leaves surrounding a short stem.
- Tendrils of peas and cucumbers are leaves. (Fig. 36.20b)
- Venus's-flytrap has leaves to trap and digest insects. (Fig. 36.20c)
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