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Objective 4:
Photophosphorylation slideshow
Photophosphoryaltion
movie handout
Photophosphorylation Schematic
(diagram used in slideshow)
Electron Transport Chains
in Photosynthesis
Objective 5:
see above
Where
do all the H+ ions come from?
Photosynthetic Phosphorylation
Objective 6:
ATP Generation by Chemiosmosis
Objective 8:
C3 v. C4 Plants
Objective 9:
The Plant Body
Ligustrum slide - available in Study Center, click here
to test yourself
What does a Ligustrum leaf look like anyway?
Zea microscope slide - available in Study Center, click here to test yourself
Kranz anatomy
Dicot v. monocot leaves
Poa slide - available in Study Center
Leaves: Minimizing Water Loss
Gas exchange in plants
Objective 10:
Functions and types of roots
Leaf demo - available in Study Center
Leaf Venation
Objective 11:
Primary growth of a root (11c)
Objective 12:
How old is that twig?
Lenticels
Twig Self Test
An example: Horse Chestnut Morphology
Objective 13:
Vascular
cambium and rays (13a,b)
Xylem and phloem in trees
Tree growth rings (13c), more optional info
Cork (13c)
Optional Supplementary Material:
The
Chemistry of Autumn Colors
Plant tissue slideshow
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Plant Tissue Slides
UNIT 4: PLANT TISSUES
| The purpose of this section of the unit is to help you become
familiar with the different types of tissues found in vascular plants.
There are many ways in which plant tissues can be classified; the one used
here is simply one of the
acceptable ones. |

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Plant tissues can be divided into two major categories: meristematic (perpetually
young tissues important in growth) and permanent tissues.
The permanent tissues fall into three subcategories: dermal, ground, and
vascular tissues.
Tissues composed of one type of cell are called simple tissues; those composed
of two
or more cell types are called complex tissues. Parenchyma, collenchyma, and
sclerenchyma are simple tissues; xylem, phloem, and epidermis are complex
tissues.
A set of slides has
been set up for you here on the course website to help visualize many of the concepts on plant growth. Use the following notes and
pages 744-754 in your text as guidelines to analyzing the
slides.
Meristematic tissues are composed of embryonic, undifferentiated (i.e., unspecialized)
cells that play a crucial role in plant growth. In plants, most of the cell
division occurs in meristematic cells that are restricted to particular regions
of the plant body. Apical meristems, found at the growing tips of stems, roots,
and in lateral buds, are responsible for the sustained increase in length of
the plant body. The tissues produced by the apical meristems are said to be
primary tissues. In many plants there are also meristematic areas towards the
periphery of the roots and stems; these lateral meristems (the vascular cambium
and cork cambium) are responsible for the sustained increase in diameter. In
both the apical and lateral meristems, certain cells are able to divide repeatedly;
after each division one of the daughter cells remains in the meristem while
the other becomes part of the plant body. The tissues produced by the lateral
meristems are said to be secondary tissues.
| Slide 1: a longitudinal section through a growing
shoot tip showing apical
meristematic tissue. Note that the cells are small, have dense cytoplasm,
and are very tightly packed. |
 |
| Slide 2: a longitudinal section through a root
tip. The meristematic
tissue is located just above the root cap. This too is apical meristem;
division of these cells followed by cell elongation results in the root
growing in length. |
| Slide 3: is primarily for orientation; it
is a cross section of a eudicot stem. Focus on the two large vascular
bundles in the center
of the slide. The xylem tissue is stained red. Just above the xylem is
a layer of meristematic tissue, the vascular cambium. The phloem tissue
is found outside of the vascular cambium. |
| Slide 4: is a high-power view of a cross-section
showing a lateral meristem, the vascular cambium, in the
same plant shown in Slide 3. Again, the xylem tissue is stained red, and
the large cells on the top
of the slide are phloem. The green brick-like cells between the xylem and
phloem is the area in which the vascular cambium is located. The new cells
produced by the cambium are initially like those of the cambium itself,
but, as they grow and mature, their characteristics slowly change as they
differentiate into other tissues. The vascular cambium is a single layer
of cells within this brick like region; it is responsible for the growth
in diameter of a stem. The tissues produced by the vascular cambium are
secondary tissues. |
| Slide 5: shows a face view of the undersurface of the epidermis of a
leaf. Most epidermal cells are relatively flat and usually the epidermis
is only
one layer thick. Here the cells are irregularly shaped and lock together
like pieces of a puzzle, leaving no intercellular spaces. Such tight connections
aid in protection against loss of water, mechanical injury, and invasion
by parasitic fungi. Notice the three stomatal openings and their associated
guard cells. |
| Slide 6: Many epidermal cells secrete a waxy, water-resistant cuticle
on their aerial parts, which minimizes water loss. Here the cuticle is
stained a pale pink. It is unusually thick in this specimen as this is
a desert plant. |
| Slide 7: Often epidermal cells are modified to form hairlike structures
and glandular hairs. These are epidermal hairs on the surface of a plant
stem. Such hairs may provide protection against insects. In some plants
the hairs are hooked and actually impale insects and larvae. |
| Slide 8: is a high-power view of one glandular
hair. Secretory hairs
may provide a chemical defense against insects. |
| Slide 9: is of another type of dermal tissue,
the outer bark or periderm (stained red in this slide). Periderm is found
on the surface of woody
plants; it includes the cork cells on the surface of older woody stems.
The periderm replaces the epidermis in plants that have secondary growth.
The cork cells are dead; it is their waterproofed cell walls that function
as the protective outer covering of plants. Meristematic cells within the
periderm (cork cambium, the other lateral meristem) produce the cork cells. |
| Slide 10: shows a cross section
of a monocot (left) and eudicot (right) stem. In a eudicot stem
there are two areas of parenchyma tissue: the cortex and pith. The cortex
is the area on the periphery of the stem, between
the epidermis and the vascular bundles. The pith is the area in the center
of the stem, inside the vascular bundles. In a monocot the vascular bundles
are scattered throughout the stem so there is no clear distinction between
pith and cortex. All of the tissue surrounding the vascular bundles is
parenchyma. Parenchyma of stems and roots functions in the storage of nutrients
and water. When turgid, parenchyma is important in giving shape and support
to the plant. |
| Slide 11: Focus on the parenchyma
cells in the pith (on the lower portion of the screen)
of the eudicot stem. Note that the cells are loosely packed and have the thin
(primary) cell walls. The parenchyma cells under the epidermis have chloroplasts
and are photosynthetic. |
| Slide 12: is a cross section of a
monocot root. The bright red cells in
a circle make up the endodermis, a tissue which in roots
separates the cortex from the vascular tissues. Inside the endodermis, the
xylem and phloem alternate with one another. The very large cells are the
xylem and the smaller green cells are phloem. Monocot roots have a pith composed
of
parenchyma
tissue
in the center of the root, inside the vascular ring, in addition to the parenchyma
tissue in the cortex. Pith and cortex are very similar, both structurally
and functionally, being distinguished from each other primarily by their
location relative to the vascular tissue. What is the primary function of
the parenchyma cells of the root? |
| Slide 13: is collenchyma tissue from
a cross section of a stalk of celery. Collenchyma cells are typically elongated.
The primary cell walls (stained light pink) are irregularly thickened, with
the walls being their thickest at the "corners" of the cell. Collenchyma
is an important supporting tissue in young plants when the cells are turgid.
(They provide good support only when hydrated.) The cells are living at maturity. |
 |
| Slide 14: is a cross section of sclerenchyma
tissue (fibers).
Note the uniformly very thickened secondary cell walls that give support
to the plant body. Here the walls are so thick that the lumen (internal space)
of the cell is nearly obliterated. These cells are dead at functional maturity. |
| Slide 15: is a longitudinal section of xylem showing the elongated
conducting cells (vessels in this case) which transport water and inorganic
materials from the roots to the leaves. These cells do not have cytoplasm
at maturity; the nucleus and cytoplasm disintegrate during development,
leaving the thick cell walls as the functional structures. Notice the pits
(holes) in the secondary walls. |
| Slide 16: shows the second vascular tissue, phloem.
The large, elongated sieve elements shown here are the actual conductive
cells; they
transport
organic materials both up and down the plant body. Sieve elements are living
cells, and very sensitive to manipulation. When this slide was made the cytoplasm
and proteins contracted and accumulated at one end of the cell, forming a "plug" (the
triangular reddish areas in the center of the slide). Note the sieve plates.
We shall learn more about the sieve elements in Unit 5. |
Once you have mastered the online slides of the various tissues, go to the
microscopes in the study center and examine the four microscope slides, using
the information
provided below.
| Slide 17: Longitudinal section of shoot tip of the houseplant Coleus,
a eudicot. The apical meristem is at the very tip of the stem, surrounded
by leaf primordia (meristematic cells that will produce leaves). The apical
meristem of the shoot is responsible for producing the cells for the primary
plant body and is involved in the formation of the leaf primordia and bud
primordia (which develop into lateral branches). Notice that the leaves
are opposite one another at the nodes, and locate the dark tissue in the
axil of each leaf, a bud primordium. The places where the leaves are attached
are known as nodes; most of the increase in length of the shoot results
from elongation of the cells of the internodes. |
| Slide 18: High power view of a longitudinal section of the Coleus apical
meristem. The apical meristem is a dome-shaped mass of dividing cells at
the tip of the shoot. The apical meristem will produce the three primary
meristems: protoderm, procambium, and ground meristem. These three meristems
in turn will produce new cells that will differentiate into the epidermis,
primary vascular tissues, and ground tissues (pith and cortex). The leaves
arise as leaf primordia along the flanks of the apical meristem and islands
of meristematic cells left behind at the bases of the leaves by the apical
meristem will become the bud primordia. Note the dark strands running into
the leaf and, more faintly, down the edges of the stem. These are the procambial
strands. Remember, all the tissues derived from the apical meristem are
primary tissue, and result in elongation of the plant shoot. |
| Slide 19: Cross-section of a Coleus stem below the apical
meristem. The more darkly-stained tissue in the stem consists of procambial
cells which appear
as a more or less continuous hollow cylinder within the ground tissue,
separating one part of the ground tissue from another. The outer ring of
ground tissue is the cortex, and the inner region is the pith. The outer
procambial cells will differentiate into primary phloem and the inner ones
into primary xylem. |
| Slide 20: Cross-section of a Coleus stem farther down the shoot. The
procambial cells continue to divide and differentiate and primary xylem
cells are easily seen in vascular bundles (particularly in the corners
of the ring). The protoderm on the surface has developed into epidermis,
and ground tissue (mostly parenchyma) forms the pith and cortex. |
| Slide 21: Cross section of herbaceous monocot and eudicot
stems. The monocot stem is on the left, the eudicot on the right. Note
that the vascular bundles
are scattered throughout the ground tissue stem in a monocot whereas they
are located in a ring in the eudicot, separating the ground tissue into
pith and cortex. The next two slides show the stems at higher magnification. |
| Slide 22: Cross section of a eudicot stem showing a
vascular bundle. The xylem (some of the vesels are stained red) is at the
bottom of the
bundle. The
phloem lies above the xylem, with a layer of vascular cambium in between. |
| Slide 23: Cross section of a vascular bundle of a monocot.
Surrounding the bundle is a sheath of sclerenchyma cells. Notice that the
bundle looks
rather like a
face. The large cells (the "eyes") which are stained red, are xylem
vessels. The green "forehead" is phloem. The larger cells in the phloem
are the sieve elements; the smaller cells are the companion cells. The "nose" area
is an airspace that is created when the first-formed xylem elements are stretched
and destroyed as the stem elongates. |
Slide 24: cross section of a dicot stem showing the vascular tissue arranged in a continuous cylinder. The red sclerenchyma cells at the top of the slide are sclerenchyma fibers of the phloem. Under the fibers lie the phloem parenchyma and the conductive phloem, the sieve tube members (stained green). Next are several layers of cells that mark the area of the vascular cambium. The xylem cells (stained red) lie below the cambium. Note the large lumens identifying some of these cells as vessel elements. The parenchyma cells in the center of the stem constitute the pith, where excretory products can be deposited.
Slide 25: cross section of a woody dicot stem in its first season of growth. Note that the xylem tissue is arranged in a continuous cylinder rather than in discrete bundles. The next slide shows the vascular tissues at a higher magnification.
Slide 26: a cross section of phloem tissue, including fibers, is at the top of the slide. The phloem fibers and the phloem cells nearest the fibers are primary phloem, those closest to the vascular cambium were produced by the cambium and are therefore secondary phloem. The vascular cambium lies at the junction where the staining changes from green and red to red. The xylem cells just below the cambium are produced by the cambium and are secondary xylem. The primary xylem can be easily located on this slide because the cells have very large lumens and are closer to the pith. Notice that the tissue on either side of the vascular cambium is secondary tissue produced by the cambium. Where would the ray initials of the cambium be located? ...the fusiform initials?
Slide 27: cross section of another dicot stem in its first year of growth. A ray system can be noted, extending throughout the secondary xylem and phloem. From outside in, locate the epidermis, cortex (with tightly packed collenchyma cells close to the epidermis and parenchyma cells inside), primary phloem, secondary phloem, vascular cambium, secondary xylem, and primary xylem. Note the vascular rays in the secondary xylem and secondary phloem. Vascular rays are radial strands of parenchyma cells that function as pathways for lateral transport of materials and as storage areas. Ray cells are produced by the ray initials in the vascular cambium.
Slide 28: high power view of a vascular ray. Locate the vascular cambium (green brick wall-like cells running from top to bottom). To the right of the cambium is the secondary xylem. To the left side is the secondary phloem. The vascular ray is funnel-shaped; it is several cell layers thick in the xylem, but expands greatly in the phloem. Some of the rays in secondary phloem will become very wide as the stem increases in girth; this is one way in which the tissues outside the cambium keep up with the increase in girth as new xylem cells are produced. Rays function in lateral transport; nutrients move through plasmodesmata from the secondary phloem through the vascular cambium to the living (parenchyma) cells of the secondary xylem. Although some water flows from the xylem to the phloem through the symplast of vascular rays, much of the water movement is through the apoplast system.
Slide 29: cross section of a woody stem in its second year of growth. The cork cambium has become active and produced the non-living cork cells on the outside of the stem. Underneath the periderm lies the phloem, the fibers of which are stained red. Inside the phloem lies the vascular cambium and internal to the cambium is the xylem. There is a small amount of pith in the center of the stem. Where would the primary phloem be located? ...the secondary phloem? ...the primary xylem? ...secondary xylem? Note the two annual rings showing that the stem is in its second year of growth. (See also Fig. 35.22, p. 754.)
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