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Pracs Weeks 1 - 6
1.
2.
3.
4.
5.
6.
Week One
ANGIOSPERM DIVERSITY
General introduction
The aim of these practicals and associated audiovisual sessions is to introduce you to the
broad diversity of angiosperms and to provide you with training in their identification. To
achieve this, you must first become familiar with the descriptive terminology used to
communicate about the variation observed in plant morphology. Once you are conversant
with botanical descriptive terminology, you should be able to identify any plant in the world, as
long as you have a (reliable) taxonomic key. Thus, we will also provide you with training in
how to use dichotomous keys as well as open-entry, interactive keys.
As with any new language, you must be prepared to practice using botanical terminology.
Therefore, throughout this component of the course, we will provide you with the opportunity
to practice your newly acquired skills by keying out plant species that we will supply.
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1.1
Whilst we have made every effort to provide material that exemplifies a particular character,
you should realise that many of the terms should be considered as points along a continuum
of morphological variation. You will discover that intermediate conditions exist!
Perhaps the best way to conceptualise plant morphology is to think of plants as being
modular in their construction (Fig 1). Notice how every module comprises a leaf and its node,
an axillary bud and an internode. The branch or stem, therefore, is made up of a number of
these modules.
Figure 1
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1.2
Similarly, inflorescences are shoots that serve for the formation of flowers. Inflorescence
characters can be very confusing due to the arbitrary separation of leaf and flower-bearing
portions of a shoot. Two fundamentally different types of inflorescence can be recognized
(Fig 2). One type is terminated by a flower, whereas the other is not. Thus we have
determinate (monotelic) and indeterminate (polytelic) inflorescences.
Figure 2
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1.3
Flowers also follow a generalized morphological pattern (Fig 3 ) which can be considered as a
series of concentric rings whorls of organs. In the case of flowers with both male and
female parts, the female reproductive structures (gynoecium) is always surrounded by the
male reproductive parts (androecium). The petals (corolla) always surround the androecium
and the sepals (calyx) always surround the corolla. Thus, the variation encountered in flowers
generally reflects the presence or absence of one of these whorls or the fusion of various
components within or between whorls. This consistency of spatial arrangement of organs
allows us to formularize the morphology of any flower.
Figure 3
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1.4
Floral formulas act as an accurate, shorthand means of conveying the form of any flower. It
relies on the use of codes arranged in a precise sequence. The following codes each refer to
the number of parts and whether they are fused within (are connate) or between (are adnate)
whorls. The sequence always follows:
1. Symmetry:
irregular
or
regular
.|.
2. Number of parts in the calyx (K)
3. Number of parts in the corolla (C)
4. Number of parts in the androecium (A)
5. Number of parts in the gynoecium (G)
6. Whether the gynoecium is:
inferior
or
superior
G
If parts are connate (i.e. fused within a whorl) they are surrounded by a circle e.g.
If parts are adnate (i.e. fused between whorls) they are linked by a line e.g.
Thus a formula of:
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1.5
Each station contains a set of tasks for you to complete. Once you have worked through the
morphological definitions, you should move onto section 2 of the practical.
Section 2
This will involve you in describing a number of rainforest plants using the terminology that you
have just defined. You will then identify the rainforest plants you have just described by using
an interactive, computerized key.
Section 3
You will describe the morphology of a flower using a standardised floral formula.
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1.6
Vegetative characters
Habit
Tree
.
.
Shrub .
.
.
Herb
.
.
Suffrutescent .
.
.
Vine
.
.
Liana .
.
.
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Leaf arrangement
Alternate
.
.
Opposite
.
.
Whorled
.
.
Pseudowhorled
.
.
Leaf structure
Simple (unlobed)
.
.
Simple (lobed)
.
.
Compound (pinnate)
.
.
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Compound (bipinnate)
.
.
Compound (palmate)
.
.
Unifoliolate
.
.
Stipules
Interpetiolar
.
.
Petiolar
.
.
Terminal
.
.
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Leaf shape
Ovate .
.
.
Obovate
.
.
Elliptic .
.
.
Oblong .
.
.
Leaf base
Acute
.
.
Rounded
.
.
Cuneate
.
.
Cordate
.
.
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Leaf tip
Acute .
.
.
Acuminate
.
.
Mucronate
.
.
Emarginate ..
.
.
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1.11
Leaf margin
Entire .
.
.
Serrate
.
.
Dentate
.
.
Crenate .
.
.
Domatia
.
.
.
Trichomes
Simple
.
.
Branched .
.
.
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1.12
Reproductive characters
Determinate inflorescences
Cyme
.
.
Raceme .
.
.
Umbel
.
.
Panicle .
.
.
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1.13
Indeterminate inflorescences
Raceme
.
.
Umbel
.
.
Head (capitulum) .
.
.
Spike
.
.
Spadix
.
.
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1.14
Inferior ovary .
.
.
Section 2
Take one piece of each rainforest plant and fill in the following table. When you have completed
the table you will be shown how to use the interactive key to rainforest plants.
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1.15
Specimen Habit
Example
tree
Leaf
arrangement
alternate
Leaf
form
Stipules
Domatia
Leaf
aroma
Oil dots
Leaf
margin
Leaf
length
mm
Leaf width
mm
simple
absent
present
present
present
entire
50-150
25-50
Gland
absent
Hairs
absent
Petiole length
mm
Other features
20-40
Leaves soft
A
B
1.16
Section 3
Take a piece of flowering stem with at least two flowers on it. Write a floral formula for the
species. We will identify the species in a subsequent practical using the key to angiosperms in
the Flora of the Sydney Region.
Floral formula:
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Contents
page
Bryophytes (Week 2)
Concepts .................................................................................................... 2.2
Practical Exercises
A. Liverworts ................................................................................. 2.3
B. Hornworts ................................................................................. 2.8
C. Mosses ..................................................................................... 2.9
Keywords ................................................................................................. 2.14
Review Questions .................................................................................... 2.15
Lycophytes and monilophytes (week 2)
Concepts .................................................................................................. 2.16
Practical Exercises
D. Psilotopsida (Monilophyte) ..................................................... 2.18
E. Lycophyta (Lycophyte) ........................................................... 2.19
Keywords ................................................................................................. 2.21
Polypodiopsida (Monilophytes) and gymnosperms (Week 3)
Concepts .................................................................................................... 3.1
Practical Exercises
A. Polypodiopsida ......................................................................... 3.1
Keywords ................................................................................................... 3.6
Review Questions ...................................................................................... 3.7
Gymnosperms (week 3)
Concepts .................................................................................................. 3.10
B. Cycadophyta ........................................................................... 3.11
C. Ginkophyta ............................................................................. 3.13
D. Pinophyta ............................................................................... 3.14
E. Gnetophyta ............................................................................. 3.15
Keywords ................................................................................................. 3.16
Review Questions .................................................................................... 3.17
Recommended books
Evert RF and Eichhorn SE. 2013. Raven: Biology of Plants. 8th Ed. Freeman & Co Publishers. New York. NY.
Online material: http://www.whfreeman.com/Catalog/static/whf/raven/
NOTE: The introductory text in the following sections on bryophytes, ferns and gymnosperms is a brief summary of
the basic structural and reproductive features in each group. In the practical exercises you will have the opportunity
to study these features in detail. It is best to read the concepts before each practical class, which will help you
understand what you are doing and allow you to make rapid progress.
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2.1
Week Two
INTRODUCTION TO BRYOPHYTES, LYCOPHYTES AND MONILOPHYTES
Concepts
Land plants. Several lines of evidence indicate that land plants evolved from a charophycean green alga.
Like the green algae, land plants have chlorophyll a (primary photosynthetic pigment), chlorophyll b and
carotenoids (accessory pigments), starch (carbohydrate reserve) deposited within the chloroplasts, and
cellulose (principal component of the cell wall).
A number of structural modifications were accomplished during the transmigration from aquatic to
terrestrial environment. Unlike the green algae (except Coleochaete), land plants form a phragmoplast
and a cell plate during cell division. The phragmoplast consists of a ring of microtubules and actin
filaments, oriented perpendicular to the equatorial plane, which expands centrifugally ahead of the cell
plate as it grows toward, and eventually fuses with, the parental cell wall. In most algae, in contrast, cell
division is accomplished by a phycoplast (microtubules oriented parallel to the new wall, the new wall
grows centripetally). All plants have embryos (hence the term embryophytes). The development of the
zygotes depends on the protective and nutritional environment of the gametophyte. One of the features
that protects the land plants from drying out is a layer(s) of sterile cells around the antheridium (pl.
antheridia; male sex organs, produce sperm) and around the archegonium (pl. archegonia; female sex
organs, produce eggs and protect the embryo). A sterile jacket layer was also formed around the sporeproducing cells of the sporangium (pl. sporangia). Land plants typically show a heteromorphic
alternation of generations. The aerial parts of most plants are covered with a waxy layer, the cuticle
(prevents dehydration), which is closely correlated with the presence of stomata (sg. stoma; gas
exchange). More advanced features include the evolution of the vascular tissue, vascular cambium,
apical and secondary meristems, and leaves.
BRYOPHYTES. Bryophytes are the simplest, least specialized, small land plants. They usually inhabit
damp environment, although some can tolerate loss of most of their cytoplasmic water and rehydrate
when water becomes available again. They have no true xylem and phloem, but they have developed
alternative ways of trapping and transporting water. The gametophyte (haploid) is always nutritionally
independent whereas the sporophyte (diploid) is permanently attached to, and dependent on, the
gametophyte. In other words, the gametophyte is the conspicuous and dominant generation, in contrast
to the dominant sporophytes of vascular plants. The gametophyte is usually attached to the substrate by
elongate single cells of filaments of cells called rhizoids, which generally serve only to anchor the plants
since absorption of water and ions commonly occurs directly through the gametophyte. Archegonia and
antheridia both have sterile jacket layers; each archegonium contains a single egg, each antheridium
produces numerous, biflagellate sperm. The sperm must swim through water to reach the archegonium.
The archegonia are flask-shaped, with a long neck and swollen basal portion, the venter, which encloses
a single egg. The central cells of the neck, the neck canal cells, disintegrate when the archegonium is
mature, resulting in a fluid-filled tube through which the sperm swim to the egg. After fertilization, the
zygote is retained within the archegonium where it develops into an embryo. The cells of the venter
divide and enlarge, and the venter keeps pace with the growth of the young sporophyte within the
archegonium; the enlarged archegonium is called calyptra. The subsequent details of development
differ among the various bryophytes.
Traditionally the term "bryophytes" has been used as a collective term for three distinct divisions of these
relatively unspecialized plants:
A.
B.
C.
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2.2
Using a dissecting microscope, examine a small sample of Marchantia and note the dark-green thallus
with a midrib-like region, air pores, and gemma cups on the upper surface.
A2. What is the function of gemmae?
Examine the lower surface and note the many rhizoids, which are tubular structures of one or more cells
that anchor the thallus to the substrate. You may also find multicellular scales on the lower surface.
A3. [slide B320]. On a prepared slide of TS Marchantia thallus, note the air pores and chambers,
chlorenchyma tissue (green), and storage tissue.
A4. As shown in the demonstration of reproductive Marchantia, the gametophytes are unisexual, with the
gametangia being borne on specialized, erect branches of the male and female plants. The antheridia
are on disk-headed branches antheriodiophores, and the archegonia on spoke-headed
archegoniophores.
A5. [slide B323B]. Examine a prepared slide with LS antheridial head and find the elongate antheridia.
Each antheridium consists of a short stalk and a mass of spermatogenous tissue surrounded by a
sterile jacket layer that is one cell thick.
A6. Are the sperm nuclei produced by meiosis or mitosis?
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2.3
Examine a prepared slide LS archegonial head [slide B325]. Locate a fully developed archegonium
and identify the swollen basal portion, or venter; the egg cell within the venter; and the elongate neck,
with its neck canal cells. The archegonium may be surrounded by a collar-shaped flap of tissue.
A9. Are the archegonia located on the upper or lower surface of the head?
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2.4
Examine the same slide under a high-power objective and identify the stalk (seta), capsule
(sporangium), numerous spores and elongated elaters, all enclosed within the sterile jacket layer of the
capsule. The elaters have hygroscopic wall thickenings that twist with changes in humidity and aid in
spore dispersal. The remnants of the old archegonium form a cap, or calyptra.
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2.5
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2.6
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2.7
Examine the demonstration microscope with a small piece of thallus dissected out. Note the number of
chloroplasts in a cell and the presence or absence of pyrenoids.
B3. What other group of plants contain pyrenoids and similar number of chloroplasts?:
Note the mode of dehiscence of the sporangium and look for the thread-like, colourless columella. Tease
out a portion of the sporangium in water on a slide and observe under a microscope.
B4. Describe the shape of the spores and the pseudo-elaters:
B5. Examine the two demonstration slides of LS young sporangium of Anthoceros [slides B300 and
B304] showing a foot, meristem tissue, developing sporogenous tissue, and columella.
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2.8
Mosses constitute a diverse group of about 10,000 species, which inhabit an amazingly wide range of
environments, from damp, tropical areas to Antarctica, and in deserts and on dry rocks. Moss
gametophytes are leafy", with the leaves usually arranged in a spiral. The sporophytes are partly
photosynthetic, differentiated into a stalk (seta) and a sporangium (capsule); there are no elaters. The
gametophyte of "true mosses" (class Bryidae, eg. Funaria, Dawsonia) first forms as a protonema, which
gives rise to a bud with an apical cell, and eventually to the leafy gametophyte. In many mosses, the
stems of the gametophytes and sporophytes have a central strand of water-conducting cells (hydroids),
which in some genera are surrounded by food-conducting cells (leptoids). The sporangia (capsules) are
generally elevated on a stalk (seta) and spore dispersal is aided by a ring of hygroscopic teeth
(peristome). Stomata are usually present on moss sporophytes although some consist only of a single,
doughnut-shaped guard cell.
The sequence of colour photographs on the large poster Life of a Moss shows the salient features of
these organisms and their reproductive cycle. The poster is complemented by a set of demonstration
slides from which the photographs were originally taken. You may notice that the principal features of the
Moss life cycle are similar to those of Marchantia that you have studied earlier. A diagram of a moss life
cycle is included on pages 2.12 & 2.13.
C1. Examine the colour photographs on the poster, comparing with the original slides if necessary, and
make brief notes about the main features in the space below.
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2.9
Some mosses have primitive conducting tissue consisting of hydroids and leptoids. Identify the rhizome
and aerial stem of live Dawsonia.
C2. Examine a prepared slide of TS aerial stem Dawsonia [slide B384]. Identify the hydroids and
leptoids:
Examine demonstration photographs of transfer cells in the foot of Dawsonia capsule. These cells have
extensive wall ingrowths, which increase the surface area/volume ratio and thus enhance the efficiency of
transport of solutes.
C3. How would you describe the shape of the ingrowths? :
Look for antheridia and archegonia in young, reproductive plants of Funaria, or a similar moss, by
dissecting the plant under a microscope (old plants will have only adult sporophytes).
C4. (slides B381 & B361B). Examine slides with LS of moss archegonia and antheridia.
Draw and label an archegonium and an antheridium. Are they different from those in the liverwort? :
Examine a mature sporophyte on a live moss. Note the capsule, calyptra, operculum, and peristome.
Breathe on the peristome teeth and with a hand-lens observe their hygroscopic movements.
C5. Which way do the peristome teeth move in high humidity? Which way do they move in dry air? :
Mosses of diverse morphologies are shown in the demonstration, including specimens with branched
gametophytes, elongated capsules, etc.
C6. Describe the apparent differences in their gametophytes and sporophytes :
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KEYWORDS
antheridiophore
antheridium
Anthoceros
apical cell
archegoniophore
archegonium (arche=beginning)
calyptra (kalyptra=covering)
capsule (capsula=little box)
cell plate
columella (columna=column)
cuticle (cutis=skin)
Dawsonia
elater (elatus=lift, carry away)
embryo
embryophyte
foot
Funaria
gemma (gemma=bud)
hornwort
hydroid
leptoid (leptos=slender)
liverwort
Marchantia
moss
neck canal
operculum (operire=lid)
peristome (peri=around)
phragmoplast (phragmos=fence)
phycoplast
pore
protonema (protos=first)
rhizoid (rhiza=root)
seta (seta=bristle)
spermatozoid (sperma=seed)
Sphagnum
spore (sporos=seed)
sporangium
sporophyte
stomata (stoma=mouth)
thallus (thallos=branch)
transfer cells
venter (venter=belly)
zygote (zygon=yoke)
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2.14
REVIEW QUESTIONS
1. Name the three groups of nonvascular plants.
2. Do the three groups have similar life cycles? What parts of the cycle are different?
5. What are the characters that distinguish nonvascular plants from algae?
7. How do liverworts differ from mosses? How do hornworts differ from both?
8. What are the morphological/anatomical differences between leafy liverworts and mosses?
14. What happens to the neck canal cells during development of the archegonium?
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2.15
20. How are the spores released from the sporophyte? Any specific mechanisms in the three groups?
21. A spore germinates into a filamentous protonema: Where does the apical cell originate? How?
25. How do the nonvascular plants deal with long-distance transport of water, minerals, and sugars?
27. What do you think is the evolutionary advantage of having a phragmoplast instead of a phycoplast?
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2.16
DIVERSITY IN TRACHEOPHYTES
A number of key advances, besides those accomplished by the bryophytes, have accompanied the early
invasion of the land by plants. These include the evolution of the shoot and efficient photosynthetic
leaves (acquisition of light energy, acquisition of carbon dioxide), roots (absorption of water and
nutrients, anchorage of the plant), and an efficient conducting system consisting of xylem (transport of
water and nutrients) and phloem (transport of assimilate), which facilitates long-distance transport.
Another important feature was the evolution of protective layers such as the cuticle and spores with
protective walls. As early plants became increasingly suited to life on land, their gametophytic
generation was progressively reduced in size and became increasingly more protected by, and
nutritionally dependent on, the dominant sporophyte. Moreover, the life cycle has acquired the selective
advantages of two new principles:
a) heterospory, the production of microspores that carry genes over large distances, and
megaspores that nourish the young embryo; and
b) endosporial development of gametophytes, which provides protection for both male and
female gametophytes and is the necessary first step in the evolution of seed plants.
Construction of the vascular column. In most ferns and fern allies, the plant body consists entirely of
primary tissues, there are no secondary meristems.
The vascular tissues exhibit three basic
arrangements:
1. Protostele, the most primitive type of stele. It consists of a solid central column of vascular tissue,
xylem surrounded by phloem. It was found in extinct vascular plants and it is present in the living
Psilotum, Lycopodium, and Selaginella. Additionally, this type of stele is found in the roots of most
living seed plants.
2. Siphonostele, a hollow vascular cylinder surrounding a parenchymatous pith. In ferns the phloem may
be inside as well as outside the cylinder together with an endodermis on both sides, in which case
the stele is called solenostele. Vascular strands (leaf traces) depart from the hollow vascular
cylinder and lead to the leaves, leaving behind open spaces (leaf gaps) in the cylinder.
3. Eustele, which consists of a system of discrete vascular strands that surround the pith, the strands
being separated from one another by ground tissue. This type is present in almost all living seed
plants.
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2.17
Origin of leaves. Leaves originated in more than one way. The following are the two most widely
accepted theories.
1. Microphylls evolved as superficial lateral outgrowths (enations) of the stem (see diagram below). An
outgrowth may or may not have a leaf trace, but if present the leaf trace does not create a leaf
gap. Microphylls are associated with protosteles and are characteristic of the lycophytes and
Psilotum (monilophytes).
2. Megaphylls, in contrast, are leaves with complex venation and the leaf traces are associated with leaf
gaps. They are associated with siphonosteles and eusteles. According to the telome theory,
megaphylls evolved by a sequence of modifications of a branch system, namely: a) "overtopping",
whereby an equal dichotomous branching becomes overtopped by one dominant branch (the main
axis) and the remaining branches become lateral; b) "planation", or flattening of all the lateral
branches into one plane; and c) "webbing", whereby a thin sheet of photosynthetic tissue
develops in the spaces between the neighboring branches.
Two additional processes,
"recurvation" and "coalescence", could explain the evolution of fertile leafy structures
(sporophylls).
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2.18
Reproduction. The life cycles of seedless vascular plants are essentially similar to one another: an
alternation of heteromorphic generations in which the sporophyte is dominant and free-living. Generally,
the gametophytes are reduced in size and dependent on food derived from the sporophyte. An important
advance, relative to bryophytes, was the evolution of heterosporous plants (e.g. Selaginella, Isoetes,
Marsillea). These produce microspores and megaspores, which germinate and give rise to male
gametophytes and female gametophytes (produce antheridia and archegonia). All seedless vascular
plants have motile sperm which require water to swim to the archegonium.
Diversity. Vascular plants go back at least 420 million years. The earliest ones, now extinct, belonged to
the division Rhyniophyta which had simple, dichotomously branching axes without roots or leaves.
Extinct Lycophyta, Equisetopisida and fern-like monilophytes were key representatives of the "Coal age
plants" 360-280 MYA, a period of great accumulation of fossil-fuel. The seedless vascular plants that live
today may be classified in four divisions:
PSILOTOPSIDA (only two living genera, Psilotum and Tmesipteris), which lack roots and usually also lack
leaves.
LYCOPHYTA (Lycopodium, homosporous;
microphylls associated with protosteles.
EQUISETOPSIDA (mostly extinct, only one living genus, Equisetum, homosporous), reduced scale-like
leaves, eustele.
POLYPODIOPSIDA (a very large group of "TRUE FERNS", eg. Polystichum, Pteridium, mostly homosporous
but some are heterosporous), have megaphylls and siphonosteles.
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2.19
As the name homosporous suggests, Lycopodium produces meiospores of only one size. Live
sporophylls are pale green and are closely compacted into an elongated cone, or strobilus (strobilos=fircone). Each sporangium originates from the cells near the base of the leaf. Numerous spore mother
cells (sporocytes) divide meiotically to form tetrads of spores.
E2. Examine a prepared slide of LS strobilus of Lycopodium [slide B458].
Note that all sporangia and the spores they contain are identical in size.
After the spores have been liberated from the sporangium, they may remain dormant for days or years but
eventually germinate to produce small, inconspicuous gametophytes. Antheridia and archegonia are
borne on the same gametophyte, usually intermingled but sometimes segregated into different areas.
After fertilization, the zygote divides transversely to the long axis of the archegonium. One daughter cell
forms a suspensor, while the other divides to form foot, stem, and root primordia. The rest of the life cycle
is similar to that in Polypodiopsida in week 3.
Traditionally the Lycophyta have served to demonstrate the evolution from homospory to heterospory.
The heterosporous Selaginella produces meiospores of two different sizes: the larger one, the
megaspore, which originates from megasporangia that are borne on megasporophylls, develops into the
female gametophyte;the smaller one, the microspore, which originates from microsporangia that are
borne on microsporophylls, develops into the male gametophyte. All sporophylls are compacted into
strobili. In some species, the lower sporophylls of the cone may bear megasporangia while the upper
ones bear microsporangia, although the spatial arrangement varies among species. The development of
both male and female gametophytes is endosporous, that is, it occurs within the confines of the spore
wall (see diagram below).
E3. Examine a prepared slide of LS strobilus of Selaginella. [slide B465A].
Note the different size of microsporangia and megasporangia, as well as different size of misrospores
(30-80 m diameter) and megaspores (150-600 m diameter).
E4. Draw a diagram of the heterosporous cone and label
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2.20
The microspore nucleus divides repeatedly, giving rise to a jacket one cell thick that surrounds the central
spermatogenous cells. Each spermatogenous cell differentiates into a disc-shaped spermatozoid with
two anterior flagella. At maturity the jacket cells break down, releasing the free-swimming spermatozoids.
KEYWORDS
annulus (ring)
antheridium
apical cell
archegonium
cuticle (cutis=skin)
dependent gametophyte
dictyostele
dominant sporophyte
eusporangium
eustele
extant species
Equisetum
frond
heterosporous plant
homosporous plant
lamina (thin plate)
leaf
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leaf gap
leaf trace
leptosporangium
(lepto=thin/fine/slender)
Lycopodium
megaphyll (megas=large/great)
megaspore
microphyll
microspore
petiole (petiol=leafstalk)
phloem
Polystichum
Pteridium (ptero=wing/feather)
prothallus (protos=first)
protostele
Psilotum (psilos=bare)
pteridophyte
Botany
rhizome (rhiza=root)
root
Selaginella
shoot
siphonostele (siphon=pipe/tube)
sorus
spores
stele (stele=standing pillar)
tapetum (tapet=carpet/rug)
thallus (thallos=young shoot)
tracheid
(tracheia=windpipe/artery)
tree-fern
xylem
vessel (vas=duct)
2.21
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2.22
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2.23
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2.24
Week Three
Examine live fern gametophytes growing in a dish (demonstration) and showing various stages of
development. The youngest ones may not have reached the reproductive stage yet; others may be
reproductive, having gametangia (archegonia and antheridia) on the lower surface; and large, mature
gametophytes may already have a young sporophyte growing alongside them.
Collect a small sample of reproductive gametophytes, place them lower surface uppermost on a
slide, and examine under your dissecting microscope. Note the position of the single apical cell in the
cleft of the heart-shaped gametophyte, rhizoids originating from the central cushion, and the relatively
thin wings.
A3. Draw the gametophyte and label
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3.1
Unlike the bryophytes, the fern gametangia occur on the same gametophyte, although they usually are
spatially separated. Typically, the archegonia are located closer to the cleft of the heart-shaped
gametophyte. On your specimen, locate the protruding archegonial necks (fertilized archegonia are
brown). Antheridia, which are more globose and usually develop before the archegonia (temporal
separation ensures outcrossing), are located among the rhizoids. Compare your specimen with the
prepared slides of antheridia [slide B405] and archegonia [slide 407] in your slide trays.
A4. Complete your drawing above in [A3] by indicating the relative positions of antheridia and archegonia
on the gametophyte.
If you have successfully located a gametophyte in the reproductive stage, it should have some antheridia
with mature spermatozoids. Place the gametophyte on a slide, mount in a drop of water under a
coverslip, tap gently with a lead pencil, and examine under 10x and 40x objectives. Mature antheridia
undergo a hypotonic shock, which releases the motile spermatozoids into the surrounding liquid
medium.
A5. Can you see them swim? How would you describe the swimming motion? :
Anatomical details of the archegonium are best seen on prepared sections. Examine the slide of LS
fern archegonium [slide LS 409] in your slide tray under a HP objective. Identify the venter, egg,
neck, and neck canal cells.
A6. Draw the archegonium and label. How does it resemble the moss archegonium you saw last week?
Following fertilization, the zygote begins to develop into an embryo, which then grows to become a
young sporophyte. Examine the demonstration slide [B415] showing a young sporophyte still attached
to the parental gametophyte. Note the primary root of the sporophyte, the region of foot (attachment to
the gametophyte), and the first leaf (megaphyll) with a dichotomous venation.
A7. Does the young sporophyte have a chance to survive out in the bush on its own? How soon? By
what means? :
Structure of the sporophyte. Despite the tender age and harsh environment, many young sporophytes
"make it" and grow into robust, mature plants.
Examine a mature sporophyte of live Polystichum with sori (demonstration plant). Identify the
underground stem (rhizome) with adventitious roots, young leaves (fiddleheads) near the apex of the
rhizome, and large, finely divided mature leaves (fronds). The frond petiole is usually covered in brown
scales, and the compound, bipinnate lamina is subdivided into leaflets (pinnae) and further into
secondary leaflets (pinnules).
A8. Draw a diagram of the sporophyte and label
Look for clusters (sori) of sporangia on the lower (abaxial) surface of the leaflets on large fronds in
various stages of maturation. Note the variation in size and colour of the sori. Immature sori are very
small and light-coloured, while the mature ones are distinct and brown. Break of a leaflet with mediumsized sori, and another leaflet with large, brown sori, and examine them both under your dissecting
microscope. Note the spatial relationship of the sori to the veins.
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3.2
A9. Are the sori associated with the veins or do they occur along the leaf margins?
(on your drawing (A8) of the sporophyte, indicate the position of sori and veins).
Continue dissecting your specimens under the microscope. A developed sorus is protected by an
umbrella-like, papery cover (indusium). Use a needle to remove the indusium from the sorus to expose
the individual, stalked sporangia. Continue searching until you find a sorus with dark-brown, mature
sporangia. If you bring your desk-lamp close to the exposed sorus, the sporangia will soon begin to dry
out and crack open to discharge the spores.
A10. How would you describe mechanistically the process you see?
Scrape mature sporangia from an intact sorus onto a slide and mount in a drop of glycerol under a
coverslip. Observe under 10x or 40x objectives. Identify the following structures: a) annulus, a
peripheral row of cells with thickened inner walls; b) stomium (a "mouth"), thin-walled cells between the
end of the annulus and the attachment of the stalk (this is where the sporangium will crack open); c)
sporangium side walls; and d) spores, located inside the sporangium. As the glycerol dehydrates the
cells of the annulus, the annulus straightens and the resulting tension opens the sporangium at the
mouth, releasing the spores. When observed under 40x objective, the individual bean-shaped spores
may be surrounded by a bulging "perine" coat or, if exposed, the spores may show a "scar" or "hilum"
(the result of attachment of spores in the tetrad).
A11. Draw the sporangium under HP and label all the details. a) Explain the mechanism of spore
dispersal in this organism. b) In what way is this mechanism similar to that in the bryophytes? c) What
type of nuclear division gives rise to the spores
Botany
3.3
Examine a prepared slide with TS sorus of Polystichum [TS indusium B432A, TS sporangia B420,
fern sporangia B431] in your slide tray. Note the sorus, indusium, and sporangia. Compare with your
own preparation above.
A12. How would you compare these details with your preparation of the fresh material?
Anatomy of the stele. A classical example of protostele was shown for Psilotum in last weeks
practical. Generally, the Pterophyta utilize a rich variety of siphonosteles. These apparently evolved
from the protostele independently from eustele, which is characteristic of all seed plants. On the other
hand, some Pterophyta such as Pteridium have evolved xylem elements that resemble the vessels of
the seed plants
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3.4
To complement the view seen in the transverse sections, examine a prepared slide with longitudinal
section of Pteridium stele LS Pteridium rhizome [slide 20] in your slide tray. Identify tracheids with
unique wall thickenings; primitive vessels with scalariform thickenings and perforations in the end wall;
and phloem elements with sieve areas. Finally, examine the slide of macerated rhizome [slide
B2400] in your slide tray to see the details of the wall architecture in the individual cell types.
Apical meristems. Theoretically, the evolution of specialized conducting cells allows more extensive
division of labor among the various tissues of the plant. Downward phloem transport permits roots to
extend deep into the dark soil, and ylem conducts water upward to the elongating shoot. Absorption of
nutrient solutions by roots, and a steady import of carbohydrate from the photosynthetic megaphyll, allow
the development of tissues that perform other specific tasks, such as that of the apical meristems. Most
ferns, however, still depend on the activities of simple apical cells similar to those seen in the
bryophytes, and unlike the more complex meristems found in the seed plants.
Examine the demonstration slide of the shoot apex of Davallia. [slide 4 on demo bench]. Note a
single apical cell. With luck, you may be able to find a procambial strand, which is the earliest visible
sign of developing vascular tissue.
A15. Draw the apical cell with the adjacent, derived, cells on either side. Indicate the location of the
procambial strand if you have found it
Botany
3.5
Examine the demonstration slide of LS Davallia root apex [slide 5 on demo bench]. Note the single
triangular apical cell, which cuts off new cells from all three faces.
A16. Draw the apical cell. How does it differ from the apical cell in the shoot? :
_________________________________________________________________________________
_________________________________________________________________________________
KEYWORDS
microphyll
microspore
petiole (petiol=leafstalk)
phloem
Polystichum
Pteridium (ptero=wing/feather)
prothallus (protos=first)
protostele
Psilotum (psilos=bare)
pteridophyte
rhizome (rhiza=root)
root
Selaginella
shoot
siphonostele (siphon=pipe/tube)
sorus
spores
stele (stele=standing pillar)
tapetum (tapet=carpet/rug)
thallus (thallos=young shoot)
tracheid (tracheia=windpipe/artery)
tree-fern
xylem
vessel (vas=duct)
annulus (ring)
antheridium
apical cell
archegonium
cuticle (cutis=skin)
dependent gametophyte
dictyostele
dominant sporophyte
eusporangium
eustele
extant species
Equisetum
frond
heterosporous plant
homosporous plant
lamina (thin plate)
leaf
leaf gap
leaf trace
leptosporangium (lepto=thin/fine/slender)
Lycopodium
megaphyll (megas=large/great)
megaspore
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3.6
REVIEW QUESTIONS
1. What makes the ferns and fern allies more advanced than the bryophytes?
2. What do the ferns and fern allies lack relative to gymnosperms?
3. What benefits can be attributed to the evolution of vascular tissue?
4. What would be the selective advantage of a tall, upright habit?
5. What is the selective advantage of a water-proofing cuticle?
6. Would it make sense to develop stomata before developing an impermeable cuticle?
7. What is the function of roots, relative to rhizoids?
8. Why should vascular tissue precede the evolution of roots and active apical meristems?
9. How could lignified cells be useful in plants?
10. How would you describe the main differences between protostele, siphonostele, and eustele?
11. Would siphonostele and eustele be superior to protostele?
12. Do any living plants have a protostele?
14. Could a protostele form a leaf trace?
15. Do angiosperms have a protostele? In roots? In stems?
16. Do tree-ferns have secondary xylem?
17. What types of cells constitute the xylem in pteridophytes?
18. It could be argued that three types of leaves occur in the plant kingdom. What are they?
19. How would you tell if a small leaf was a microphyll rather than a megaphyll?
20. What is the differences between enation and telome?
21. What is the significance of the microphyll- and megaphyll-lines of evolution?
22. Why is Psilotum regarded as a living fossil?
23. What was the problem with the cambium in ancient lycophytes?
24. What has been the most significant change in gametophyte morphology since 420 MYA?
25. How would you compare the evolutionary potential of haploid and diploid organism?
26. What are the reproductive constraints in ferns and their allies, relative to gymnosperms?
27. What is the significance of heterospory?
28. What is the meaning of "primitive" and "advanced" in describing plant features?
29. Why are the terms "original" (or "relictual") and "derived" more accurate?
30. Why do we study pteriodophytes?
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3.7
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3.8
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3.9
GYMNOSPERMS
One of the most important innovations to arise during the evolution of vascular plants was the seed and
the pollen grain. The seed provides protection for the enclosed embryo, and the stored food supports
the germination and establishment of the seedling, thus giving the seed plants a great selective
advantage.
Another crucial evolutionary advance compared with ferns was the bifacial vascular
cambium. This is a secondary meristem, which produces secondary xylem (in gymnosperms mostly
tracheids with circular bordered pits); secondary phloem (sieve cells, but no companion cells in
gymnosperms); and a secondary meristem, cork cambium.
Unlike fertilization in mosses and ferns, the male gametes of gymnosperms travel by a
combination of two unique means of transport. First, pollination, which is accomplished by various
transport mechanisms of the pollen grain from the microsporangium to the megasporangium. This is
followed by the formation of a pollen tube (male gametophyte), in which two male gametes (sperm)
arise directly from the spermatogenous cell (antheridia are lacking in all seed plants). The pollen tube
carries the two male gametes to the archegonium. Subsequently, one sperm of the pollen tube unites
with the egg inside the archegonium, while the second sperm has no apparent function in gymnosperms.
Thus, free water is no longer necessary for the sperm to reach the egg. Except for cycads and Gingko,
which have flagellated sperm, the sperm of seed plants are non-motile.
Structural diversity in gymnosperms. Living gymnosperms may be classified into four divisions,
although they all have similar life cycles.
CYCADOPHYTA (cycads, eg. Cycas, Zamia, Macrozamia)
GINKGOPHYTA (Ginkgo)
PINOPHYTA (very large group of conifers: eg. Araucaria, Pinus, Callitris)
GNETOPHYTA (Gnetum, Ephedra, Welwitschia)
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3.10
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3.11
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3.12
There are two demonstration microscope slides of Macrozamia, showing important stages of the
reproductive cycle. Examine demonstration slide LS ovule with mature archegonium [slide B469] on
demo bench, and locate the following: pollen chamber, archegonial chamber, archegonia, and
megasporangium/nucellus.
B1. Draw a diagram of the ovule. Label which components are diploid & which are haploid.
Examine demonstration slide LS pollen tubes in nucellus [slide 3] on demo bench showing the
antherozoid nuclei and archegonial necks.
B2. Identify all of the above features .
Similarly to the cycads, the Ginkgophyta once had many genera and species. Today the only surviving
relic is a single species, Ginkgo biloba, the maidenhair tree. It has been saved from extinction by the
priests of ancient China and Japan who cultivated the trees in their temple gardens. The maidenhair
tree is planted extensively for decoration now. The tree is deciduous, dioecious, with short "spur" shoots
with microsporangiate cones produced by the males, and "long" shoots with ovuliferous structures
produced by the females.
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3.13
Exercise D: Pinophyta (allow 1 hour) (observe live plant & demonstration materials)
From the four divisions, the conifers are the largest and most widespread group, with about 500 species
dominating vast areas of the northern cool temperate forests and representing about one third of all
earth forest. The tallest vascular plant, the redwood (Sequoia), which grows up to 117 m tall and over 11
m in diameter, is a conifer. Other conifer genera include Abies (fir), Picea (spruce), Pinus (pine), and
Araucaria (Norfolk Island pine), which is restricted to the Southern Hemisphere. This division also
includes Wollemia nobilis (the Wollemi pine) that belongs to the family Araucariaceae. Morphological
studies of wood anatomy DNA analysis suggest that the Wollemi is a new genus, falling between Agathis
and Araucaria.
There are various examples of gymnosperms and cones in the laboratory for you to examine. Also,
there is a large, colour poster of Life of a Pine on display. The pictures and accompanying text describe
the basic morphological and anatomical features of the organism and its life cycle. It is a simple way of
learning the important principles of a gymnosperm life cycle. Below are specific tasks and questions for
you to answer, as well as extra space for any additional notes you may wish to take.
Examine the details of the structure of the male cone.
D1. How would you describe the composition of the pine wood?
D3. Would you find both male and female cones on the same branch?
D4. What are the sacs on the lower side of the microsporophylls?
D5. Are the ovules located on the upper or the lower surface of the ovulate scales?
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3.14
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3.15
KEYWORDS
Araucaria
bifacial vascular cambium
cambium (cambium=change)
cone (konos=cone)
conifer
Pinophyta
cork cambium
Cycadophyta
endospory (endon=within/inside)
gamete (gametes=spouse)
gametophyte
generative cell/nucleus
Gingko
Gnetophyta
gymnosperm (gymnos=naked)
heteromorphic
heterospory
integument (inter=between)
long shoot
Macrozamia
megaspore
megaspore wall
megagametophyte
megasporophyll
microspore
microgametophyte
microsporophyll
nucellus
ovule (ovum=egg)
ovuliferous scale
Pinus
pollen chamber
pollen grain
pollen tube
secondary meristem
secondary phloem
secondary xylem
seed
seed coat
Sequoia
short shoot
sieve cell
sperm (sperma=seed)
spermatogenous cell
sporophyte (sporos=seed)
suspensor
sterile cell
tube cell/nucleus
tracheid (trachia=windpipe)
vessel (vas=vessel)
xylem
REVIEW QUESTIONS
1. Many conifers have only small scale- or needle-like leaves. Are these microphylls? Why?
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3.16
8. What is wood?
12. Are conifer cones similar to those of lycophytes? How do they differ?
13. What are the differences between conifer and cycad cones?
14. How can you tell the difference between microsporophyll and megasporophyll?
19. What are the advantages of retaining the megaspore by the sporophyte?
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3.17
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3.18
Week Four
SYSTEMATICS
Aims
In todays practical you will develop hypotheses about the evolutionary relationships of
Eucalyptus and Angophora, by carrying out a phylogenetic analysis of selected species.
Throughout the exercises you should be developing a working knowledge of the
vocabulary of systematics.
Objectives
After completing this practical and the associated reading you should be able to:
1. do an analysis of characters to resolve relationships amongst Eucalyptus and
Angophora.
2. devise a phylogenetic classification for Eucalyptus and Angophora.
3. interpret a cladogram.
4. correctly use the vocabulary of systematics (e.g. apomorphy, synapomorphy,
plesiomorphy, ancestral, derived, character, character state, cladogram).
5. construct a phylogeny for a group of organisms of your choice.
Introduction
There is a wonderful diversity of life, both living and extinct. For biologists to easily
communicate with each other about these organisms they need to be classified into
groups. Ideally, the classification should be based on the evolutionary history of life, such
that it predicts properties of newly discovered or poorly known organisms. Classification,
however, is only one aspect of the much larger field of systematics. Systematics is an
attempt to understand the evolutionary interrelationships of living things and systematists
try to interpret the way in which life has diversified and changed over time. The aims of
systematics can be summarised as:
To discover ALL of the branches of the evolutionary tree of life.
To document ALL changes that have taken place during the evolution of those braches
To describe ALL of the species (the tips of the branches).
Systematics then, is the study of the pattern of relationships amongst taxa (groups of
organisms). Taxonomy is a subsidiary discipline of systematics and involves the theory
and practice of describing and naming taxa and is currently based on a system developed
by Linnaeus in the 18th century. Contemporary taxonomists attempt to make their
classifications natural by making them congruent with hypotheses on the evolutionary
relationships of the taxa they are concerned with.
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4.1
PRINCIPLES OF CLADISTICS
Cladistics has been defined as the concepts and methods employed for the determination
of the branching patterns of evolution (Stuessy 1990). The results of a cladistic analysis
are represented by a branching diagram a cladogram - which, in turn, economically
summarises a number of evolutionary trees or hypotheses. Optimally, cladograms are
bifurcating networks which define nested sets of taxa on the basis of shared, derived
characters. Furthermore, nested sets of taxa are, ideally, monophyletic; that is, they share
a common ancestor. Thus, a cladogram may represent the phylogenetic relationships of
the group under study. If a classification is based upon this branching pattern, the
classification may, also, be thought to represent the phylogeny of the group, and, hence
be a natural classification.
Procedure:
Cladograms can be represented as nested sets of taxa, with each set being defined by
shared derived characters. For example the relationships illustrated as a nested set below
can be represented by the following data set. A simple example of a set of characters and
their states is outlined in the Table 1.
1, 2
4, 5
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4.2
Characters
Species
outgroup
Table 1. A data matrix recording the states of nine characters (A-I) for five species (1-5)
and an outgroup.
Thus, by reference to Table 1 we can see that the species-group 1, 2, 3, 4 and 5 is defined
by character A, the species-group 1 and 2 is defined by character B, the species-group 3,
4, and 5 is defined by character C (as well as by lacking character B) and species-group 4
and 5 is defined by character D. Characters E - I are unique to the species which possess
them, therefore, these characters do not define relationships between species, they only
define the species themselves. So, to construct a cladogram we first look for groups of
taxa defined by shared characters, then, within those groups, identify sub-groups based
on other shared characters. Things are not, however, that simple, for we must also decide
whether the shared characters are derived or ancestral. In other words, we must be able
to identify if an evolutionary change occurred along the branch that leads to each group of
species.
How can we distinguish ancestral from derived characters?
We need to polarise the characters into ancestral and apomorphic derived states. Then
we need to see if the derived states are shared by any of the species-groups. This is most
commonly achieved by the use of an outgroup.
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4.3
4
H
I
D
B
C
A
Figure 1. A cladogram based on the data in Table 1 upon which the characters have beenI
mapped. I = shared derived characters (synapomorphies). II = unique characters
(autapomorphies). NB: The outgroup is not shown in this figure.
Having drawn a cladogram (Fig. 1), we can map the characters that define speciesgroups (i.e. synapomorphies) onto the appropriate branches of the cladogram. The
theoretical position of characters unique to the terminal taxa (i.e. autapomorphies) can
also indicated; note that these characters do not define relationships.
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4.4
Once the synapomorphies are mapped on, we can easily determine the phylogenetic
length of our cladogram by counting the total number of evolutionary steps (characters
state changes) required to give the particular cladogram branching pattern (usually
referred to as a topology). In Figure 1 we can see that the length of the tree is 9 steps (i.e.
4 synapomorphies + 5 autapomorphies). We could, also, say that only four characters
were informative (the four synapomorphies).
Botany
4.5
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4.6
Biological nomenclature
Our current system of nomenclature is based on a system invented by Linnaeus in the
18th century (the Linnean system). The scientific name of a species includes the name of
the genus to which the species belongs (the generic name) and the species epithet.
Together these are known as the species name. In our case, Homo is the name of the
genus to which the species sapiens has been assigned. The first letter of the genus name
is always capitalised; the first letter of the species epithet is always in lower case; and both
names are italicised (when typed) or underlined (when hand-written). Each taxon has a
name and a rank. The rank is a level in the hierarchical classification. There are rules
designed to ensure that every taxon has a single, unambiguous name. Similarly, each
name, at each rank from family and above has a particular ending that identifies the name
as belonging to that rank the rules of nomenclature can be found in International Code
for Botanical Nomenclature.
Kingdom
Plantae
Phylum
Magnoliophyta (ophyta)
Class
Magnoliopsida (opsida)
Order
Proteales (ales)
Family
Proteaceae (aceae)
Genus
Telopea
Species
Telopea speciosissima
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4.7
Exercise 1:
Phylogenetic relationships of Eucalyptus and Angophora
In this exercise you will explore the pattern of relationships amongst Eucalyptus and
Angophora. The principles used in this exercise can be applied to any organisms.
STEP 1.
The first step is simply to record the character states for each character in the attached
data matrix. We recommend that you examine more than one specimen or consult the
posters as well as the specimens. Enter the species name and subgenus name of each
specimen in the table.
We can indicate evolutionary change by comparing character states in the ingroup (i.e.
Eucalyptus and Angophora) with those in an outgroup (i.e. Arillastrum gummiferum). The
character states that occur in both groups are deemed to have evolved before the
separation of these two groups (i.e. are ancestral and coded 0); and those that are
different in the ingroup and the outgroup are deemed to have evolved within the ingroup
after their separation from the outgroup (i.e. are derived and coded 1). Arillastrum
gummiferum, a species endemic to New Caledonia, is proposed here as the outgroup for
this analysis. We could have also used the following species as outgroups: Arillastrum
papuana, Allosyncarpia ternata, Stockwellia quadrifida and Eucalyptopsis alauda.
Taxa
NB. The infrageneric classification follows Pryor and Johnson
Arillastrum gummiferum (outgroup)
Angophora hispida
Angophora floribunda
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4.8
Characters
NB. We have provided you with illustrations of ArilIlastrum gummiferum (Fig. 4).
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
1.
11.
12.
versatile (pivoting)
1.
Inflorescence position:
Locule number:
0.
axillary
0.
2 locules
1.
terminal
1.
>2 locules
13.
Bristle glands:
0.
opposite
0.
absent
1.
alternate
1.
present
14.
Paratracheal parenchyma:
0.
not calyptrate
0.
scanty
1.
calyptrate
1.
confluent
Bud scar:
0.
absent
15.
1.
present
0.
absent
1.
present
present
1.
suppressed
0.
not urn-shaped
Inflorescence structure:
1.
urn-shaped
0.
compound
1.
simple
16.
17.
Fruit shape:
1.
strongly longitudinally
ribbed
Anther shape:
0.
oblong (cuboid)
1.
reniform (kidney-shaped)
Anthers dehiscence:
0.
1.
Cotyledon shape:
0.
kidney-shaped (reniform)
1.
not kidney-shaped
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4.9
Figure 3. 1. Bud showing scar left by calycine operculum (E. cinerea). 2. LS of bud showing
inflexed stamens (E. sideroxylon). 3. LS of bud (E. gummifera) showing calycine operculum
(S) and Coraline operculum (P). 4. TS of flower showing the 5-loculate gynoecium (E.
saligna).
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9
5
6
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4.11
Figure 5. The floral morphology of Eucalyptus. Taken from Figs. 81, 82 & 84
(Clarke and Lee, 1987).
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4.12
STEP 2.
BUILDING A CLADOGRAM
Now that you have scored each of the eucalypts for each of the characters you will build a
cladogram to show relationships.
Fill in the Subset Chart below the data matrix with those groups that can be defined by having
a (derived) character state (coded as 1) in common. For example, Eucalyptus subgen.
Corymbia and Angophora share: bristle galnds, large oil daucts and paratracheal parenchyma
- they are thus all scored as 1. So, for this character, the subset would be BCDE.
Draw your tree as a Cladogram of Eucalyptus and Angophora with a soft pencil. Start with
the character that is the most common, i.e. identifies the largest subset of species, and show
the species that have this character as a polychotomy (or polytomy). Then repeat with the
character that is the second most common, and break up the polychotomy into two groups on
the basis of this character. Repeat until you have used all of the characters.
If the characters do not allow you to break up a cluster of organisms, you will have to leave the
cladogram with a polychotomy, where three or more species come off from the same node.
This means that the relationships among these species remain unresolved.
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4.13
Data matrix
Arillastrun
gummiferum
Fruit ribbed
Fruit urn-shaped
9 10 11 12 13 14 15 16 17
Para
parenchyma
Large oil ducts
Bristle glands
Infl. position
Anth.
dehiscence
Cotyledon
shape
Anther versatile
Anther shape
Infl. simple
locule number
Bud scar
present
Petals absent
leaf
arrangement
Perianth fused
1
Leaf venation
Characters
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IJ
Botany
9 10 11 12 13 14 15 16 17
IJ
EF GH
GH
AB AB AB
CD CD CD
4.14
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4.15
Exercise 2:
Placing new taxa into a phylogenetic analysis
A common event in systematics is for new organisms (or characters) to be found and
incorporated into the classification scheme. The best way to do this is to perform a new
analysis. In this case we will use the same characters as before but add a number of new
species. Assign character states for the five species listed below in the character matrix.
Then build a new cladogram in the same way as before, combining these five species with the
previous ten and using Arillastrum as the outgroup.
Taxa
K
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4.16
Fruit ribbed
Arillastrun
gummiferum
Fruit urn-shaped
9 10 11 12 13 14 15 16 17
Para
parenchyma
Large oil ducts
Bristle glands
Infl. position
Anth.
dehiscence
Cotyledon
shape
Anther versatile
Anther shape
Infl. simple
locule number
Bud scar
present
Petals absent
leaf
arrangement
Perianth fused
1
Leaf venation
9 10 11 12 13 14 15 16 17
EFG
HKL
MN
Species
scoring 1 for
this character
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4.18
Exercise 3:
Producing a phylogenetic classification
One of the goals of phylogenetic systematics is to produce classifications that reflect our
perceptions of evolutionary (i.e. natural) relationships. The production of phylogenetic
classifications from cladograms follows a few simple conventions:
1. Only monophyletic groups should be recognised (i.e. exclude polyphyletic and
paraphyletic taxa).
2. To indicate the tree topology, use an indenting system in the classification. In other
words, the name of each component clade is indented relative to the name of the parent
clade. Thus, sister clades/taxa are shown at the same level of indentation.
Following these conventions, it should be possible to reconstruct a phylogenetic tree that
represents any classificatory scheme. Conversely, you should be able to derived an indented
classification from any cladogram.
The classification shown below is that of Pryor and Johnson (1971) for Eucalyptus and
Angophora. It was not developed in a phylogenetic context, but it is an excellent attempt at
recognising natural groups within Eucalyptus the natural grouping are recognised at the rank
of subgenus and section.
Family Myrtaceae
Genus Arillastrum
Genus Angophora
Genus Eucalyptus
Subgenus Eudesmia
Subgenus Corymbia
Sect. Ochraria
Sect. Rufaria
Subgenus Nothocalyptus
Subgenus Symphyomrytus
Sect. Transversaria
Sect. Adnataria
Subgenus Eucalyptus
Sect Renantheria
You have two tasks:
1. DRAW a cladogram that exactly reflects the classification shown above, and then compare
this cladogram to the one you produced in Exercise 2.
2. Following the rules above, write a classification for Eucalyptus and Angophora species that
exactly reflects the cladogram you produced in Exercise 2. Write in brackets those characters
that are synapomorphies for each group.
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4.20
A new Key will be supplied at the practical for identification of these families.
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Week Six
A new Key will be supplied at the practical for identification of these families.
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6.1