PLANT KINGDOM 23

C HAPTER 3
PLANT KINGDOM
3.1 Algae In the previous chapter, we looked at the broad classification of living
organisms under the system proposed by Whittaker (1969) wherein he
3.2 Bryophytes
suggested the Five Kingdom classification viz. Monera, Protista, Fungi,
3.3 Pteridophytes Animalia and Plantae. In this chapter, we will deal in detail with further
classification within Kingdom Plantae popularly known as the ‘plant
3.4 Gymnosperms
kingdom’.
3.5 Angiosperms We must stress here that our understanding of the plant kingdom
has changed over time. Fungi, and members of the Monera and Protista
having cell walls have now been excluded from Plantae though earlier
classifications placed them in the same kingdom. So, the cyanobacteria
that are also referred to as blue green algae are not ‘algae’ any more. In
this chapter, we will describe Algae, Bryophytes, Pteridophytes,
Gymnosperms and Angiosperms under Plantae .
Let us also look at classification within angiosperms to understand
some of the concerns that influenced the classification systems. The
earliest systems of classification used only gross superficial morphological
characters such as habit, colour, number and shape of leaves, etc. They
were based mainly on vegetative characters or on the androecium
structure (system given by Linnaeus). Such systems were artificial; they
separated the closely related species since they were based on a few
characteristics. Also, the artificial systems gave equal weightage to
vegetative and sexual characteristics; this is not acceptable since we know
that often the vegetative characters are more easily affected by
environment. As against this, natural classification systems developed,
which were based on natural affinities among the organisms and consider,

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24 BIOLOGY

not only the external features, but also internal features, like ultra-
structure, anatomy, embryology and phytochemistry. Such a
classification for flowering plants was given by George Bentham and
Joseph Dalton Hooker.
At present phylogenetic classification systems based on
evolutionary relationships between the various organisms are acceptable.
This assumes that organisms belonging to the same taxa have a common
ancestor. We now use information from many other sources too to help
resolve difficulties in classification. These become more important when
there is no supporting fossil evidence. Numerical Taxonomy which is
now easily carried out using computers is based on all observable
characteristics. Number and codes are assigned to all the characters and
the data are then processed. In this way each character is given equal
importance and at the same time hundreds of characters can be
considered. Cytotaxonomy that is based on cytological information like
chromosome number, structure, behaviour and chemotaxonomy that
uses the chemical constituents of the plant to resolve confusions, are also
used by taxonomists these days.

3.1 ALGAE
Algae are chlorophyll-bearing, simple, thalloid, autotrophic and largely
aquatic (both fresh water and marine) organisms. They occur in a
variety of other habitats: moist stones, soils and wood. Some of them
also occur in association with fungi (lichen) and animals (e.g., on sloth
bear).
The form and size of algae is highly variable, ranging from colonial
forms like Volvox and the filamentous forms like Ulothrix and Spirogyra
(Figure 3.1). A few of the marine forms such as kelps, form massive plant
bodies.
The algae reproduce by vegetative, asexual and sexual methods.
Vegetative reproduction is by fragmentation. Each fragment develops into
a thallus. Asexual reproduction is by the production of different types of
spores, the most common being the zoospores. They are flagellated
(motile) and on germination gives rise to new plants. Sexual reproduction
takes place through fusion of two gametes. These gametes can be
flagellated and similar in size (as in Ulothrix) or non-flagellated (non-motile)
but similar in size (as in Spirogyra). Such reproduction is called
isogamous. Fusion of two gametes dissimilar in size, as in species of
Eudorina is termed as anisogamous. Fusion between one large, non-
motile (static) female gamete and a smaller, motile male gamete is termed
oogamous, e.g., Volvox, Fucus.

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Figure 3.1 Algae : (a) Green algae (i) Volvox (ii) Ulothrix
(b) Brown algae (i) Laminaria (ii) Fucus (iii) Dictyota
(c) Red algae (i) Porphyra (ii) Polysiphonia

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Algae are useful to man in a variety of ways. At least a half of the total
carbon dioxide fixation on earth is carried out by algae through
photosynthesis. Being photosynthetic they increase the level of dissolved
oxygen in their immediate environment. They are of paramount
importance as primary producers of energy-rich compounds which form
the basis of the food cycles of all aquatic animals. Many species of Porphyra,
Laminaria and Sargassum are among the 70 species of marine algae
used as food. Certain marine brown and red algae produce large amounts
of hydrocolloids (water holding substances), e.g., algin (brown algae) and
carrageen (red algae) which are used commercially. Agar, one of the
commercial products obtained from Gelidium and Gracilaria are used to
grow microbes and in preparations of ice-creams and jellies. Chlorella a
unicellular alga rich in proteins is used as food supplement even by space
travellers. The algae are divided into three main classes: Chlorophyceae,
Phaeophyceae and Rhodophyceae.

3.1.1 Chlorophyceae
The members of chlorophyceae are commonly called green algae. The
plant body may be unicellular, colonial or filamentous. They are usually
grass green due to the dominance of pigments chlorophyll a and b. The
pigments are localised in definite chloroplasts. The chloroplasts may be
discoid, plate-like, reticulate, cup-shaped, spiral or ribbon-shaped in
different species. Most of the members have one or more storage bodies
called pyrenoids located in the chloroplasts. Pyrenoids contain protein
besides starch. Some algae may store food in the form of oil droplets.
Green algae usually have a rigid cell wall made of an inner layer of cellulose
and an outer layer of pectose.
Vegetative reproduction usually takes place by fragmentation or by
formation of different types of spores. Asexual reproduction is by
flagellated zoospores produced in zoosporangia. The sexual reproduction
shows considerable variation in the type and formation of sex cells and it
may be isogamous, anisogamous or oogamous. Some commonly found
green algae are: Chlamydomonas, Volvox, Ulothrix, Spirogyra and Chara
(Figure 3.1a).

3.1.2 Phaeophyceae
The members of phaeophyceae or brown algae are found primarily in
marine habitats. They show great variation in size and form. They range
from simple branched, filamentous forms (Ectocarpus) to profusely
branched forms as represented by kelps, which may reach a height of
100 metres. They possess chlorophyll a, c, carotenoids and xanthophylls.
They vary in colour from olive green to various shades of brown depending
upon the amount of the xanthophyll pigment, fucoxanthin present in

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them. Food is stored as complex carbohydrates, which may be in the

form of laminarin or mannitol. The vegetative cells have a cellulosic wall
usually covered on the outside by a gelatinous coating of algin. The
protoplast contains, in addition to plastids, a centrally located vacuole
and nucleus. The plant body is usually attached to the substratum by a
holdfast, and has a stalk, the stipe and leaf like photosynthetic organ –
the frond. Vegetative reproduction takes place by fragmentation. Asexual
reproduction in most brown algae is by biflagellate zoospores that are
pear-shaped and have two unequal laterally attached flagella.
Sexual reproduction may be isogamous, anisogamous or oogamous.
Union of gametes may take place in water or within the oogonium
(oogamous species). The gametes are pyriform (pear-shaped) and bear
two laterally attached flagella. The common forms are Ectocarpus, Dictyota,
Laminaria, Sargassum and Fucus (Figure 3.1b).

3.1.3 Rhodophyceae
The members of rhodophyceae are commonly called red algae because of
the predominance of the red pigment, r-phycoerythrin in their body. Majority
of the red algae are marine with greater concentrations found in the warmer
areas. They occur in both well-lighted regions close to the surface of water
and also at great depths in oceans where relatively little light penetrates.
The red thalli of most of the red algae are multicellular. Some of them
have complex body organisation. The food is stored as floridean starch
which is very similar to amylopectin and glycogen in structure.
The red algae usually reproduce vegetatively by fragmentation. They
reproduce asexually by non-motile spores and sexually by non-motile

TABLE 3.1 Divisions of Algae and their Main Characteristics

Classes Common Major Stored Cell Wall Flagellar Habitat

Name Pigments Food Number and
Position of
Insertions
Chlorophyceae Green Chlorophyll Starch Cellulose 2-8, equal, Fresh water,
algae a, b apical brackish water,
salt water
Phaeophyceae Brown Chlorophyll Mannitol, Cellulose 2, unequal, Fresh water
algae a, c, laminarin and algin lateral (rare) brackish
fucoxanthin water, salt
water
Rhodophyceae Red Chlorophyll Floridean Cellulose, Absent Fresh water
algae a, d, starch pectin and (some),
phycoerythrin poly brackish
sulphate water, salt
esters water (most)

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gametes. Sexual reproduction is oogamous and accompanied by complex

post fertilisation developments. The common members are: Polysiphonia,
Porphyra (Figure 3.1c), Gracilaria and Gelidium.

3.2 B RYOPHYTES

Bryophytes include the various mosses and liverworts that are found
commonly growing in moist shaded areas in the hills (Figure 3.2).

Antheridiophore
Archegoniophore

Gemma cup Gemma cup

Rhizoids Rhizoids
(a) (b)

Antheridial
Capsule branch Branches

Sporophyte
Seta

Leaves

Archegonial
branch

Gametophyte
Main axis
Rhizoids

(d)
(c)

Figure 3.2 Bryophytes: A liverwort – Marchantia (a) Female thallus (b) Male thallus
Mosses – (c) Funaria, gametophyte and sporophyte (d) Sphagnum
gametophyte

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 PLANT KINGDOM 29

Bryophytes are also called amphibians of the plant kingdom because

these plants can live in soil but are dependent on water for sexual
reproduction. They usually occur in damp, humid and shaded localities.
They play an important role in plant succession on bare rocks/soil.
The plant body of bryophytes is more differentiated than that of algae.
It is thallus-like and prostrate or erect, and attached to the substratum
by unicellular or multicellular rhizoids. They lack true roots, stem or
leaves. They may possess root-like, leaf-like or stem-like structures. The
main plant body of the bryophyte is haploid. It produces gametes, hence
is called a gametophyte. The sex organs in bryophytes are multicellular.
The male sex organ is called antheridium. They produce biflagellate
antherozoids. The female sex organ called archegonium is flask-shaped
and produces a single egg. The antherozoids are released into water where
they come in contact with archegonium. An antherozoid fuses with the
egg to produce the zygote. Zygotes do not undergo reduction division
immediately. They produce a multicellular body called a sporophyte.
The sporophyte is not free-living but attached to the photosynthetic
gametophyte and derives nourishment from it. Some cells of the
sporophyte undergo reduction division (meiosis) to produce haploid
spores. These spores germinate to produce gametophyte.
Bryophytes in general are of little economic importance but some
mosses provide food for herbaceous mammals, birds and other animals.
Species of Sphagnum, a moss, provide peat that have long been used as
fuel, and as packing material for trans-shipment of living material because
of their capacity to hold water. Mosses along with lichens are the first
organisms to colonise rocks and hence, are of great ecological importance.
They decompose rocks making the substrate suitable for the growth of
higher plants. Since mosses form dense mats on the soil, they reduce the
impact of falling rain and prevent soil erosion. The bryophytes are divided
into liverworts and mosses.

3.2.1 Liverworts
The liverworts grow usually in moist, shady habitats such as banks of
streams, marshy ground, damp soil, bark of trees and deep in the woods.
The plant body of a liverwort is thalloid, e.g., Marchantia. The thallus is
dorsiventral and closely appressed to the substrate. The leafy members
have tiny leaf-like appendages in two rows on the stem-like structures.
Asexual reproduction in liverworts takes place by fragmentation of
thalli, or by the formation of specialised structures called gemmae
(sing. gemma). Gemmae are green, multicellular, asexual buds, which
develop in small receptacles called gemma cups located on the thalli.
The gemmae become detached from the parent body and germinate to
form new individuals. During sexual reproduction, male and female sex

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organs are produced either on the same or on different thalli. The

sporophyte is differentiated into a foot, seta and capsule. After meiosis,
spores are produced within the capsule. These spores germinate to form
free-living gametophytes.

3.2.2 Mosses
The predominant stage of the life cycle of a moss is the gametophyte which
consists of two stages. The first stage is the protonema stage, which
develops directly from a spore. It is a creeping, green, branched and
frequently filamentous stage. The second stage is the leafy stage, which
develops from the secondary protonema as a lateral bud. They consist of
upright, slender axes bearing spirally arranged leaves. They are attached
to the soil through multicellular and branched rhizoids. This stage bears
the sex organs.
Vegetative reproduction in mosses is by fragmentation and budding
in the secondary protonema. In sexual reproduction, the sex organs
antheridia and archegonia are produced at the apex of the leafy shoots.
After fertilisation, the zygote develops into a sporophyte, consisting of a
foot, seta and capsule. The sporophyte in mosses is more elaborate than
that in liverworts. The capsule contains spores. Spores are formed after
meiosis. The mosses have an elaborate mechanism of spore dispersal.
Common examples of mosses are Funaria, Polytrichum and Sphagnum
(Figure 3.2).

3.3 PTERIDOPHYTES
The Pteridophytes include horsetails and ferns. Pteridophytes are used
for medicinal purposes and as soil-binders. They are also frequently grown
as ornamentals. Evolutionarily, they are the first terrestrial plants to
possess vascular tissues – xylem and phloem. You shall study more about
these tissues in Chapter 6. The pteridophytes are found in cool, damp,
shady places though some may flourish well in sandy-soil conditions.
You may recall that in bryophytes the dominant phase in the life
cycle is the gametophytic plant body. However, in pteridophytes, the
main plant body is a sporophyte which is differentiated into true root,
stem and leaves (Figure 3.3). These organs possess well-differentiated
vascular tissues. The leaves in pteridophyta are small (microphylls) as
in Selaginella or large (macrophylls) as in ferns. The sporophytes bear
sporangia that are subtended by leaf-like appendages called
sporophylls. In some cases sporophylls may form distinct compact
structures called strobili or cones (Selaginella, Equisetum). The
sporangia produce spores by meiosis in spore mother cells. The spores
germinate to give rise to inconspicuous, small but multicellular,

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PLANT KINGDOM 31

Strobilus

Node

Internode

Branch

Rhizome

(b)

(d)
(c)

Figure 3.3 Pteridophytes : (a) Selaginella (b) Equisetum (c) Fern (d) Salvinia

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32 BIOLOGY

free-living, mostly photosynthetic thalloid gametophytes called

prothallus. These gametophytes require cool, damp, shady places to
grow. Because of this specific restricted requirement and the need for
water for fertilisation, the spread of living pteridophytes is limited and
restricted to narrow geographical regions. The gametophytes bear male
and female sex organs called antheridia and archegonia, respectively.
Water is required for transfer of antherozoids – the male gametes released
from the antheridia, to the mouth of archegonium. Fusion of male gamete
with the egg present in the archegonium result in the formation of zygote.
Zygote thereafter produces a multicellular well-differentiated sporophyte
which is the dominant phase of the pteridophytes. In majority of the
pteridophytes all the spores are of similar kinds; such plants are called
homosporous. Genera like Selaginella and Salvinia which produce
two kinds of spores, macro (large) and micro (small) spores, are known
as heterosporous. The megaspores and microspores germinate and give
rise to female and male gametophytes, respectively. The female
gametophytes in these plants are retained on the parent sporophytes
for variable periods. The development of the zygotes into young embryos
take place within the female gametophytes. This event is a precursor to
the seed habit considered an important step in evolution.
The pteridophytes are further classified into four classes: Psilopsida
(Psilotum); Lycopsida (Selaginella, Lycopodium), Sphenopsida (Equisetum)
and Pteropsida (Dryopteris, Pteris, Adiantum).

3.4 G YMNOSPERMS
The gymnosperms (gymnos : naked, sperma : seeds) are plants in which
the ovules are not enclosed by any ovary wall and remain exposed, both
before and after fertilisation. The seeds that develop post-fertilisation, are
not covered, i.e., are naked. Gymnosperms include medium-sized trees
or tall trees and shrubs (Figure 3.4). One of the gymnosperms, the giant
redwood tree Sequoia is one of the tallest tree species. The roots are
generally tap roots. Roots in some genera have fungal association in the
form of mycorrhiza (Pinus), while in some others (Cycas) small specialised
roots called coralloid roots are associated with N2- fixing cyanobacteria.
The stems are unbranched (Cycas) or branched (Pinus, Cedrus). The leaves
may be simple or compound. In Cycas the pinnate leaves persist for a few
years. The leaves in gymnosperms are well-adapted to withstand extremes
of temperature, humidity and wind. In conifers, the needle-like leaves
reduce the surface area. Their thick cuticle and sunken stomata also
help to reduce water loss.

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The gymnosperms are heterosporous; they produce

haploid microspores and megaspores. The two kinds of
spores are produced within sporangia that are borne
on sporophylls which are arranged spirally along an axis
to form lax or compact strobili or cones. The strobili
bearing microsporophylls and microsporangia are
called microsporangiate or male strobili. The
microspores develop into a male gametophytic
generation which is highly reduced and is confined to
only a limited number of cells. This reduced
gametophyte is called a pollen grain. The development
of pollen grains take place within the microsporangia. (a)
The cones bearing megasporophylls with ovules or
megasporangia are called macrosporangiate or female
strobili. The male or female cones or strobili may be
borne on the same tree (Pinus). However, in cycas male
cones and megasporophylls are borne on different trees.
The megaspore mother cell is differentiated from one of
the cells of the nucellus. The nucellus is protected by
envelopes and the composite structure is called an
ovule. The ovules are borne on megasporophylls which
may be clustered to form the female cones. The
megaspore mother cell divides meiotically to form four
megaspores. One of the megaspores enclosed within the
megasporangium develops into a multicellular female
gametophyte that bears two or more archegonia or
female sex organs. The multicellular female gametophyte
is also retained within megasporangium. (b)
Unlike bryophytes and pteridophytes, in
gymnosperms the male and the female gametophytes
do not have an independent free-living existence. They Dwarf Shoot
remain within the sporangia retained on the
sporophytes. The pollen grain is released from the
microsporangium. They are carried in air currents and Long Shoot
come in contact with the opening of the ovules borne
on megasporophylls. The pollen tube carrying the
male gametes grows towards archegonia in the ovules
and discharge their contents near the mouth of the Seeds
archegonia. Following fertilisation, zygote develops
into an embryo and the ovules into seeds. These seeds (c)
are not covered. Figure 3.4 Gymnosperms: (a) Cycas
(b) Pinus (c) Ginkgo

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3.5 ANGIOSPERMS

Unlike the gymnosperms where the ovules are naked, in the angiosperms
or flowering plants, the pollen grains and ovules are developed in
specialised structures called flowers. In angiosperms, the seeds are
enclosed in fruits. The angiosperms are an exceptionally large group of
plants occurring in wide range of habitats. They range in size from the
smallest Wolffia to tall trees of Eucalyptus (over 100 metres). They provide
us with food, fodder, fuel, medicines and several other commercially
important products. They are divided into two classes : the dicotyledons
and the monocotyledons (Figure 3.5).

(a) (b)
Figure 3.5 Angiosperms : (a) A dicotyledon (b) A monocotyledon

S UMMARY

Plant kingdom includes algae, bryophytes, pteridophytes, gymnosperms

and angiosperms. Algae are chlorophyll-bearing simple, thalloid,
autotrophic and largely aquatic organisms. Depending on the type of
pigment possesed and the type of stored food, algae are classfied into
three classes, namely Chlorophyceae, Phaeophyceae and Rhodophyceae.
Algae usually reproduce vegetatively by fragmentation, asexually by
formation of different types of spores and sexually by formation of gametes
which may show isogamy, anisogamy or oogamy.
Bryophytes are plants which can live in soil but are dependent on
water for sexual reproduction. Their plant body is more differentiated
than that of algae. It is thallus-like and prostrate or erect and attached to
the substratum by rhizoids. They possess root-like, leaf-like and stem-

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 PLANT KINGDOM 35

like structures. The bryophytes are divided into liverworts and mosses.
The plant body of liverworts is thalloid and dorsiventral whereas mosses
have upright, slender axes bearing spirally arranged leaves. The main
plant body of a bryophyte is gamete-producing and is called a
gametophyte. It bears the male sex organs called antheridia and female
sex organs called archegonia. The male and female gametes produced
fuse to form zygote which produces a multicellular body called a
sporophyte. It produces haploid spores. The spores germinate to form
gametophytes.
In pteridophytes the main plant is a sporophyte which is differentiated
into true root, stem and leaves. These organs possess well-differentiated
vascular tissues. The sporophytes bear sporangia which produce spores.
The spores germinate to form gametophytes which require cool, damp
places to grow. The gametophytes bear male and female sex organs called
antheridia and archegonia, respectively. Water is required for transfer of
male gametes to archegonium where zygote is formed after fertilisation.
The zygote produces a sporophyte.
The gymnosperms are the plants in which ovules are not enclosed by
any ovary wall. After fertilisation the seeds remain exposed and therefore
these plants are called naked-seeded plants. The gymnosperms produce
microspores and megaspores which are produced in microsporangia and
megasporangia borne on the sporophylls. The sporophylls –
microsporophylls and megasporophylls – are arranged spirally on axis
to form male and female cones, respectively. The pollen grain germinates
and pollen tube releases the male gamete into the ovule, where it fuses
with the egg cell in archegonia. Following fertilisation, the zygote develops
into embryo and the ovules into seeds.
The angiosperms are divided into two classes – the dicotyledons and
the monocotyledons.

EXERCISES

1. What is the basis of classification of algae?

2. When and where does reduction division take place in the life cycle of a
liverwort, a moss, a fern, a gymnosperm and an angiosperm?
3. Name three groups of plants that bear archegonia. Briefly describe the
life cycle of any one of them.
4. Mention the ploidy of the following: protonemal cell of a moss; primary
endosperm nucleus in dicot, leaf cell of a moss; prothallus cell of a ferm;
gemma cell in Marchantia; meristem cell of monocot, ovum of a liverwort,
and zygote of a fern.

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5. Write a note on economic importance of algae and gymnosperms.

6. Both gymnosperms and angiosperms bear seeds, then why are they
classified separately?
7. What is heterospory? Briefly comment on its significance. Give two
examples.
8. Explain briefly the following terms with suitable examples:-
(i) protonema
(ii) antheridium
(iii) archegonium
(iv) diplontic
(v) sporophyll
(vi) isogamy
9. Differentiate between the following:-
(i) red algae and brown algae
(ii) liverworts and moss
(iii) homosporous and heterosporous pteridophyte
10. Match the following (column I with column II)
Column I Column II
(a) Chlamydomonas (i) Moss
(b) Cycas (ii) Pteridophyte
(c) Selaginella (iii) Algae
(d) Sphagnum (iv) Gymnosperm
11. Describe the important characteristics of gymnosperms.

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