Diagram illustrating the alternation of generations life cycle in plants showing haploid gametophyte and diploid sporophyte stages with examples from Bryophytes, Pteridophytes, Gymnosperms, and Angiosperms for NEET biology.
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Plants Kingdom – Complete NEET Notes | For Free

1. Introduction to Plant Kingdom

The concept of plant kingdom classification has evolved over the years as scientific knowledge has expanded. In earlier times, organisms such as fungi and certain members of the Monera and Protista kingdoms were included in Plantae because they possessed cell walls. However, further research revealed major differences in their cellular structure, reproduction, and metabolism, which led to their removal from the plant kingdom. One such example is cyanobacteria, previously called blue-green algae. Though they resemble algae in appearance, they are now placed under Monera because they are prokaryotic. Therefore, the modern plant kingdom is now limited to five major groups: algae, bryophytes, pteridophytes, gymnosperms, and angiosperms.

Initially, plants were classified based on visible external features such as size, shape, color, number of leaves, type of habit (tree, shrub, herb), and flower parts. This system was called the artificial classification system, and one of its most notable contributors was Carl Linnaeus. In these methods, even the structure of the androecium (male reproductive part of the flower) was often the only criterion used. However, these systems had serious limitations. Since they focused on a limited number of traits, many closely related species were separated, and unrelated ones were grouped together. Moreover, these methods gave equal importance to vegetative and reproductive features, which was problematic because vegetative traits are often influenced by environmental conditions and may not reflect a plant’s true evolutionary background.

To overcome the flaws of artificial systems, scientists developed the natural classification system, which aimed to group plants based on a broader range of characteristics. This method considered both external features and internal structures, such as embryology, anatomy, phytochemistry, and overall morphology. It provided a more accurate understanding of natural relationships among plant species. One of the most accepted natural systems for flowering plants was given by George Bentham and Joseph Dalton Hooker, whose work is still respected in botanical studies. Natural classification helped organize plants based on genuine similarities, leading to better taxonomic grouping and understanding.

Today, the most widely accepted system is the phylogenetic classification system, which is based on the principle of evolutionary relationships. According to this method, organisms that belong to the same taxonomic group have a common ancestor. This approach uses evidence from fossil records, molecular biology, and DNA sequencing to establish the genetic relationships between different groups of plants. The phylogenetic system reflects the true evolutionary history of plants and offers the most logical grouping based on descent and diversification. It is more scientific and reliable compared to earlier methods.

Modern plant taxonomy has benefited from advances in computer technology. One such method is numerical taxonomy, where scientists assign numerical values and codes to a wide range of observable characteristics. These data are then analyzed using computers. This system gives equal importance to every character, and it allows researchers to evaluate hundreds of features at once. Numerical taxonomy helps achieve a more objective and consistent classification, especially when plants show overlapping traits.

In addition to morphology and evolution, modern taxonomy also uses cellular and chemical data to classify plants more accurately.

  • Cytotaxonomy focuses on the number, structure, and behavior of chromosomes during cell division. These traits are often stable and provide deep insights into relationships between species.
  • Chemotaxonomy involves the study of chemical compounds like alkaloids, terpenes, flavonoids, and other secondary metabolites found in plants. These chemicals often act as biochemical markers that help distinguish between similar-looking plants.

These advanced methods are especially helpful when fossil records are missing or when external characteristics do not provide enough distinction between species. Together, they make classification more accurate, scientific, and evolutionary.

Conclusion – The Modern Plant Kingdom

The modern understanding of the plant kingdom classification is based on a combination of old and new scientific methods. From basic visual identification to advanced molecular analysis, classification has become a complex but highly accurate process. The five key groups that are now officially part of the plant kingdom are algae, bryophytes, pteridophytes, gymnosperms, and angiosperms. Each group represents a unique level of plant evolution, starting from simple aquatic organisms to highly evolved flowering plants with fruits and seeds. Today’s classification systems are not just based on what plants look like, but also on how they function, how they evolved, and what lies within their cells. This comprehensive approach helps scientists, students, and researchers understand the incredible diversity of the plant world in a logical and evolutionary manner.

2. Introduction to Algae – Structure, Types & Reproduction

Algae are simple, chlorophyll-containing, autotrophic organisms that are mostly found in aquatic habitats, both freshwater and marine. However, they are not restricted to water bodies only – they also grow on moist surfaces such as stones, soil, wood, and sometimes live in association with fungi (like in lichens) or with animals (such as on the body of a sloth bear). Their body structure, also called thallus, is usually undifferentiated and shows no true roots, stems, or leaves.

Algae show a wide range in form and size. For example, some are colonial like Volvox, while others are filamentous like Ulothrix and Spirogyra. In some marine algae like kelps, the body becomes very large and massive.

Algae reproduce in three ways: vegetative, asexual, and sexual reproduction.

  • In vegetative reproduction, the algal body breaks into fragments, and each fragment grows into a new thallus.
  • In asexual reproduction, spores are formed, usually zoospores, which are motile (with flagella) and develop into new individuals after germination.
  • In sexual reproduction, two gametes fuse to form a zygote. Gametes may be:
    • Isogamous – gametes are similar in size and shape. They may be motile (e.g., Ulothrix) or non-motile (e.g., Spirogyra).
    • Anisogamous – gametes are unequal in size but both are motile, as seen in Eudorina.
    • Oogamous – one gamete is large and non-motile (female), and the other is small and motile (male), e.g., in Volvox and Fucus.

Algae are extremely important ecologically and economically. Through photosynthesis, algae perform nearly 50% of the total CO₂ fixation on Earth, contributing significantly to the production of oxygen and supporting aquatic life. As primary producers, they are the base of aquatic food chains and provide energy-rich compounds needed by other organisms.

Many algae are used as human food, especially marine algae like Porphyra, Laminaria, and Sargassum. A total of about 70 marine algae species are edible. Some algae like brown and red algae are also sources of hydrocolloids (water-holding substances) such as algin (from brown algae) and carrageen (from red algae), which are widely used in industrial applications.

A well-known product obtained from red algae (Gelidium and Gracilaria) is agar, used as a medium to grow microbes in labs and in making ice-creams and jellies. Another important unicellular alga is Chlorella, which is rich in proteins and used as a nutritional supplement, even by space travellers.

Algae are broadly classified into three main groups based on the pigments they contain and other biochemical and structural characteristics:

  1. Chlorophyceae (Green Algae)
  2. Phaeophyceae (Brown Algae)
  3. Rhodophyceae (Red Algae)

Chlorophyceae, commonly known as green algae, are a group of simple aquatic photosynthetic organisms that appear bright green in colour due to the presence of chlorophyll a and chlorophyll b. These pigments are not scattered randomly but are contained within clearly defined chloroplasts, which come in various shapes depending on the species — such as discoid, plate-like, reticulate (net-like), cup-shaped, spiral, or even ribbon-shaped.

The structure of green algae can vary:

  • Some are unicellular (single-celled),
  • Others form colonies (groups of cells living together),
  • And some exist as filaments (thread-like chains of cells).

Within their chloroplasts, green algae often contain special storage bodies called pyrenoids, which are rich in proteins and help store starch. In some species, oil droplets are also stored as reserve food material.

Their cell wall is quite tough and layered — the inner layer is made of cellulose, which provides rigidity, while the outer layer contains pectose, a jelly-like substance that helps in absorption and protection.

Green algae can reproduce in three different ways:

  1. Vegetative reproduction – This usually happens through fragmentation, where the algal body breaks into smaller parts, and each part grows into a new individual.
  2. Asexual reproduction – This takes place through the formation of motile spores called zoospores. These are flagellated (tail-like structures for movement) and are produced inside zoosporangia (special spore-forming structures).
  3. Sexual reproduction – This mode of reproduction is diverse in green algae and can occur in any of the following forms:
    • Isogamous – where the fusing gametes are identical in size and shape.
    • Anisogamous – where the gametes are unequal in size but may both be motile.
    • Oogamous – where a large, non-motile female gamete fuses with a small, motile male gamete.

Some of the most commonly found examples of green algae include:

  • Chlamydomonas (unicellular and motile),
  • Volvox (colonial and motile),
  • Ulothrix (filamentous and non-motile),
  • Spirogyra (filamentous with spiral chloroplasts),
  • Chara (macroscopic and highly organized green alga).

Phaeophyceae, commonly known as brown algae, are mostly found in marine environments, especially along cold coastal waters. These algae display a wide range of forms and sizes. Some species are simple and filamentous like Ectocarpus, while others like kelps can grow to enormous lengths — even up to 100 meters, forming large, branched structures.

The brown colour of these algae is due to the presence of xanthophyll pigment called fucoxanthin, along with chlorophyll a, chlorophyll c, carotenoids, and other xanthophylls. Depending on the amount of fucoxanthin, their colour can vary from olive green to dark brown.

In terms of food storage, brown algae do not store simple sugars. Instead, they accumulate complex carbohydrates like laminarin and mannitol as reserve food materials. Their vegetative cells are surrounded by a cell wall made of cellulose, which is coated externally with a gelatinous layer of algin — a substance that holds water and gives a slimy texture.

Inside the cells, the protoplast contains a centrally located vacuole, plastids, and a nucleus. The body structure of brown algae is well organized — it is usually attached to a substratum (surface) by a holdfast (like a root), followed by a stipe (stalk-like structure), and ends in a broad, flat, leaf-like frond which performs photosynthesis.

Brown algae reproduce in three major ways:

  1. Vegetative reproduction – occurs by fragmentation, where the thallus breaks into pieces, and each piece develops into a new organism.
  2. Asexual reproduction – mostly takes place by biflagellate zoospores, which are pear-shaped (pyriform) and possess two unequal flagella attached on the sides.
  3. Sexual reproduction – shows isogamy, anisogamy, or oogamy, depending on the species. In oogamous species, the fusion of gametes may happen either in water or inside the oogonium (female reproductive organ). The gametes are also pear-shaped and have two laterally attached flagella for movement.

Some of the well-known examples of brown algae include:

  • Ectocarpus (simple filamentous form),
  • Dictyota (branched thallus),
  • Laminaria (large kelp-like algae),
  • Sargassum (floating seaweed),
  • and Fucus (flat, leathery thallus).

Rhodophyceae, commonly known as red algae, are easily recognized by their distinct reddish colour, which comes from the pigment r-phycoerythrin. This red pigment is dominant and helps them absorb light even in deep ocean waters where very little sunlight penetrates. Although some species can be found near the surface, a large number of red algae are marine and are more commonly found in the warm coastal regions of the sea.

Most red algae have multicellular bodies, and in some cases, their body structure is quite complex. Their thallus (body) may appear as soft filaments or as large, leathery sheets, depending on the species. Unlike green or brown algae, the food in red algae is stored in the form of floridean starch, which is chemically similar to amylopectin and glycogen – both are complex carbohydrates that serve as energy reserves.

When it comes to reproduction, red algae do not have motile reproductive cells:

  • Vegetative reproduction occurs by fragmentation, where a piece of the thallus breaks off and grows into a new organism.
  • Asexual reproduction happens through non-motile spores, which are released into the water and germinate into new individuals.
  • Sexual reproduction in red algae is always oogamous, meaning it involves the fusion of a large non-motile female gamete with a smaller male gamete, which is also non-motile. This process is followed by complex post-fertilisation developments, which help form the next generation.

Some of the common and important examples of red algae include:

  • Polysiphonia – filamentous red algae with branched structure,
  • Porphyra – used as food (especially in sushi sheets),
  • Gracilaria – a source of agar used in microbial cultures,
  • Gelidium – another major source of commercial agar used in food and research industries.

3. Bryophytes – Non-Vascular Plants and Their Classification

Bryophytes are non-vascular land plants that include mosses and liverworts. These plants are most commonly found in moist, shaded, and hilly areas. Because they grow on land but require water for sexual reproduction, they are known as the “amphibians of the plant kingdom”. Their unique requirement for water ties them closely to damp environments, where they help in primary succession, i.e., the gradual formation of ecosystems on bare rocks or soil.

The plant body of bryophytes is more advanced than algae but still relatively simple. It is thallus-like, meaning undifferentiated into true root, stem, and leaf, and can be prostrate (lying flat) or erect. It attaches to the surface using structures called rhizoids, which can be unicellular or multicellular. Although they lack true roots, stems, and leaves, some bryophytes may have leaf-like, root-like, or stem-like parts.

The main plant body of a bryophyte is haploid and is responsible for producing gametes, which is why it is referred to as the gametophyte. The reproductive organs in bryophytes are multicellular. The male reproductive organ is called an antheridium, and it produces biflagellate sperm cells called antherozoids. The female reproductive organ is the archegonium, which is flask-shaped and contains a single egg cell.

For fertilization, water is essential — the antherozoids swim through water to reach the archegonium. Once the male gamete fuses with the egg, a zygote is formed. Interestingly, the zygote does not divide immediately by meiosis. Instead, it grows into a multicellular diploid body called the sporophyte. This sporophyte remains attached to the gametophyte (it is not free-living) and depends on it for nutrition because the gametophyte is photosynthetic.

Within the sporophyte, some cells undergo meiosis (reduction division) to produce haploid spores. These spores germinate and give rise to new gametophyte plants, thus completing the life cycle.

Though bryophytes do not have vast economic importance, they are ecologically very significant. Some mosses serve as food for herbivorous mammals, birds, and other animals. A notable moss called Sphagnum is used to produce peat, which has long been utilized as fuel and as a packing material for transporting live plants and materials due to its excellent water-retention capacity.

Bryophytes are also pioneer species — they are among the first organisms to colonize bare rocks alongside lichens. They play a vital role in soil formation by breaking down rock surfaces over time and making the area suitable for the growth of higher plants. Moreover, dense mats of mosses reduce the force of falling raindrops and help in preventing soil erosion.

Based on their structure and features, bryophytes are broadly classified into two major groups:

  1. Liverworts
  2. Mosses

Liverworts are non-vascular plants that generally grow in moist and shady areas, such as near streams, wet soil, marshy places, tree bark, and dense forests. Their structure is simple and usually thalloid, meaning their plant body looks like a flat, green sheet that stays close to the surface it grows on. A good example is Marchantia. This thallus is dorsiventral (it has a distinct upper and lower side) and remains tightly attached to the ground. Some liverworts appear leafy with small leaf-like outgrowths arranged in two rows on either side of a stem-like structure.

Liverworts reproduce asexually through two main methods:

  1. Fragmentation – where the thallus breaks into pieces and each piece grows into a new plant.
  2. Gemmae formationGemmae (singular: gemma) are small, green, multicellular asexual reproductive bodies. These develop in tiny structures called gemma cups, present on the surface of the thallus. Once mature, gemmae detach from the parent and develop into new individual plants.

In sexual reproduction, liverworts produce male and female sex organs, either on the same thallus (monoecious) or on different thalli (dioecious). After fertilization, a sporophyte develops, which is structurally divided into three parts:

  • Foot (anchors the sporophyte to the gametophyte),
  • Seta (a stalk), and
  • Capsule (where spores are formed).

Inside the capsule, meiosis occurs and haploid spores are formed. These spores are released and germinate into new, independent gametophyte plants, thus completing the life cycle.


Mosses are non-vascular plants belonging to the division Bryophyta and form a vital link in the life cycle between algae and vascular plants. They are mostly found in moist, shaded environments and play a crucial role in soil formation and preventing erosion.


  • The gametophyte is the dominant, photosynthetic, and independent stage of mosses.
  • The gametophyte has two distinct stages:
    1. Protonema Stage:
      • Develops directly from the spore.
      • Creeping, green, filamentous and branched structure.
      • Often resembles filamentous green algae.
    2. Leafy Stage:
      • Arises from secondary protonema as a lateral bud.
      • Consists of upright, slender axis with spirally arranged leaves.
      • Anchored to the soil by multicellular, branched rhizoids.
      • Bears the male (antheridia) and female (archegonia) sex organs.

  • Occurs through:
    • Fragmentation of the leafy gametophyte.
    • Budding in the secondary protonema.

2. Sexual Reproduction:

  • Sex organs are borne at the apex of the leafy shoots:
    • Antheridia (male)
    • Archegonia (female)
  • Fertilization requires water for the sperm to reach the egg.
  • The zygote develops into a sporophyte.

  • The sporophyte is partially dependent on the gametophyte.
  • It is more developed in mosses compared to liverworts.
  • Consists of:
    • Foot (attaches to gametophyte)
    • Seta (stalk)
    • Capsule (sporangium where spores are produced)
  • Spores are produced after meiosis inside the capsule.
  • Mosses possess an elaborate mechanism for spore dispersal.

  • Funaria
  • Polytrichum
  • Sphagnum

  • Help in soil formation by breaking down rocks.
  • Retain moisture and prevent soil erosion.
  • Used as bioindicators of pollution.
  • Sphagnum moss is economically important (used as peat).

4. Pteridophytes – First Vascular Plants and Their Adaptations

Pteridophytes are a group of vascular, seedless plants that include important genera like horsetails and ferns. They represent the earliest land plants to develop true vascular tissuesxylem and phloem, enabling efficient water and nutrient transport. This evolutionary advancement distinguishes them from bryophytes. Pteridophytes usually thrive in cool, damp, and shaded environments, although some species can adapt to sandy soils as well. These plants hold ecological and economic significance, as they are often used for medicinal purposes, serve as soil binders, and are popular as ornamental plants.

Unlike bryophytes, where the gametophyte is the dominant life stage, in pteridophytes, the sporophyte is the dominant and independent phase. The sporophyte is differentiated into true roots, stems, and leaves, all of which contain well-developed vascular tissues. Based on the size and complexity of leaves, pteridophytes may have either microphylls (small leaves, as seen in Selaginella) or macrophylls (large leaves, like in ferns). The leaves bear sporangia that are associated with special structures known as sporophylls—leaf-like appendages that protect the reproductive organs. In some plants, these sporophylls form compact cone-like structures called strobili, as observed in Selaginella and Equisetum.

The sporangia produce haploid spores through meiosis in spore mother cells. These spores germinate to form tiny, multicellular, free-living, and photosynthetic structures called prothalli, which represent the gametophyte generation. The gametophytes require a moist, shaded environment to survive, as water is essential for the fertilization process. The gametophyte bears male and female sex organs—antheridia and archegonia, respectively. Male gametes or antherozoids are released from antheridia and swim in water to reach the archegonium, where fertilization occurs. The resulting zygote develops into a new sporophyte, thus completing the life cycle.

Most pteridophytes are homosporous, meaning they produce only one type of spore that gives rise to bisexual gametophytes. However, some genera like Selaginella and Salvinia are heterosporous, producing microspores (male) and megaspores (female). These spores develop into male and female gametophytes, respectively. An important evolutionary feature of heterosporous pteridophytes is that the female gametophyte remains attached to the parent sporophyte, allowing the zygote to develop into an embryo within the female tissue. This adaptation marks an evolutionary step toward the seed habit, which later appears in gymnosperms and angiosperms.

Pteridophytes are broadly classified into four main classes based on their morphological and structural traits:

  1. Psilopsida – e.g., Psilotum
  2. Lycopsida – e.g., Selaginella, Lycopodium
  3. Sphenopsida – e.g., Equisetum
  4. Pteropsida – e.g., Dryopteris, Pteris, Adiantum

5. Gymnosperms – Naked Seed Plants and Reproductive Structures

Gymnosperms are a group of seed-producing vascular plants whose seeds remain naked, i.e., not enclosed within any fruit or ovary wall. The term ‘Gymnosperm’ itself is derived from Greek, where gymnos means naked and sperma means seed. In these plants, the ovules remain exposed before and after fertilisation, and the seeds that develop later are also not enclosed. Gymnosperms are predominantly medium to tall trees and shrubs, with notable examples like the giant redwood tree (Sequoia), which ranks among the tallest living plant species.

Gymnosperms have a tap root system. In some genera like Pinus, the roots form symbiotic associations with fungi, known as mycorrhiza, which aids in nutrient absorption. In others, such as Cycas, specialized roots called coralloid roots house nitrogen-fixing cyanobacteria, enabling the plant to thrive in poor soils. The stem in gymnosperms may be unbranched, as seen in Cycas, or branched, like in Pinus and Cedrus. Leaves can be simple or compound. In Cycas, the pinnate leaves are long-lasting. In conifers, needle-like leaves are adapted to survive in extreme climates. These adaptations include a thick cuticle, sunken stomata, and reduced surface area, all of which help minimize water loss in dry, cold, or windy environments.

Gymnosperms are heterosporous, meaning they produce two types of haploid sporesmicrospores (male) and megaspores (female). These spores develop inside sporangia borne on modified leaves called sporophylls, which are arranged in cones or strobili. Male cones, known as microsporangiate strobili, carry microsporangia on microsporophylls, where microspores develop into pollen grains. The male gametophyte is highly reduced and non-motile, confined within the pollen grain. This development occurs inside the microsporangia.

The female cones, called megasporangiate or macrosporangiate strobili, bear megasporophylls which carry ovules containing megasporangia. In Pinus, male and female cones occur on the same plant (monoecious), while in Cycas, they are found on separate plants (dioecious). Inside each ovule, a megaspore mother cell undergoes meiosis to form four haploid megaspores, of which only one survives to develop into the female gametophyte. This gametophyte remains embedded within the nucellus and bears archegonia—the female sex organs.

Unlike bryophytes and pteridophytes, the male and female gametophytes of gymnosperms are not free-living. They remain confined within their respective sporangia, attached to the sporophyte. During fertilization, pollen grains are released from the microsporangia and are carried by air currents to the micropyle (opening) of the ovule. A pollen tube grows from the pollen grain toward the archegonium and delivers the non-motile male gametes, enabling fertilization of the egg cell. Post-fertilization, the zygote develops into an embryo, and the ovule matures into a seed. These seeds remain naked, without any protective fruit covering.


  • Seed-bearing but non-flowering plants.
  • Naked seeds (no fruit formation).
  • Tap root system with mycorrhiza (Pinus) or coralloid roots (Cycas).
  • Heterosporous: Microspores (pollen) and megaspores (ovules).
  • Strobili (cones) for reproduction.
  • Non-motile sperm delivered via pollen tube.
  • No independent gametophyte; gametophytes develop within cones.
  • Examples: Pinus, Cycas, Cedrus, Sequoia.

Gymnosperms mainly belong to the division Pinophyta, with common classes like:

  • Cycadopsida (Cycas)
  • Ginkgopsida (Ginkgo biloba)
  • Coniferopsida (Pinus, Cedrus, Sequoia)
  • Gnetopsida (Gnetum, Ephedra)

6. Angiosperms – Flowering Plants with Enclosed Seeds

Angiosperms, also known as flowering plants, represent the most advanced and diverse group in the plant kingdom. Unlike gymnosperms, in which the ovules remain exposed, angiosperms are characterized by the presence of flowers – specialized reproductive structures where both pollen grains and ovules develop. One of the defining features of angiosperms is that their seeds are enclosed within a fruit, which develops from the ovary after fertilization. This enclosure not only protects the developing embryo but also aids in seed dispersal through various agents like wind, water, and animals. Angiosperms are incredibly diverse and can be found in a wide variety of habitats – from aquatic environments to arid deserts. They display an extensive range in size, from microscopic plants like Wolffia, the smallest flowering plant, to gigantic trees like Eucalyptus, which can grow over 100 meters tall. Their ecological and economic importance is immense; angiosperms provide humans with essential resources including food grains, vegetables, fruits, fodder for animals, timber, fibers, oils, medicines, spices, and numerous industrial products. Based on the number of cotyledons in the seed, angiosperms are classified into two major groups: Dicotyledons, which possess two cotyledons, and Monocotyledons, which have only one. These two groups differ not only in seed structure but also in leaf venation, vascular bundle arrangement, root type, floral parts, and germination patterns. Overall, angiosperms dominate terrestrial vegetation and play a vital role in maintaining ecological balance and supporting life on Earth.


7. Chapter Summary – Key Concepts and Important Points at a Glance

The plant kingdom is broadly classified into five major groups: algae, bryophytes, pteridophytes, gymnosperms, and angiosperms, each representing a distinct evolutionary level of plant development. Algae are the simplest, predominantly aquatic, autotrophic organisms that contain chlorophyll and exhibit a thalloid body structure. They are classified into Chlorophyceae, Phaeophyceae, and Rhodophyceae, based on their pigment composition and the nature of stored food. Algae reproduce through various methods: vegetative reproduction by fragmentation, asexual reproduction via different types of spores, and sexual reproduction, which may involve isogamy, anisogamy, or oogamy.

Bryophytes represent the first land plants that still depend on water for sexual reproduction. Their plant body is more differentiated than algae and consists of structures resembling roots, stems, and leaves. They are non-vascular and attach to the substrate using rhizoids. Bryophytes are grouped into liverworts and mosses. Liverworts have a dorsiventral thalloid body, while mosses exhibit upright axes with spirally arranged leaf-like structures. The dominant stage in their life cycle is the gametophyte, which bears the male (antheridia) and female (archegonia) sex organs. Fertilization leads to the formation of a diploid zygote, which develops into a sporophyte that remains attached to the gametophyte and produces haploid spores for reproduction.

Pteridophytes are the first vascular plants with well-developed roots, stems, and leaves, all containing vascular tissues like xylem and phloem. The main plant body is a sporophyte, which bears sporangia that produce haploid spores by meiosis. These spores germinate into independent, photosynthetic, thalloid gametophytes known as prothalli, which require cool, moist environments. Gametophytes produce antheridia and archegonia. Water is essential for fertilization, where male gametes swim toward archegonia to fertilize the egg, forming a zygote that develops into a new sporophyte.

Gymnosperms are seed-producing plants in which the ovules remain exposed, both before and after fertilization, hence the term naked-seeded plants. These are typically medium to tall trees or shrubs like Pinus, Cycas, and Sequoia. They exhibit a dominant sporophytic phase with well-developed tap roots, often associated with mycorrhizal fungi or nitrogen-fixing cyanobacteria in coralloid roots. Leaves are adapted to extreme conditions, with needle-like forms, thick cuticles, and sunken stomata. Gymnosperms are heterosporous, producing microspores and megaspores in male and female cones (strobili), respectively. Male gametophytes are represented by pollen grains, which are carried by wind to the ovule. Fertilization occurs through the pollen tube, and the zygote develops into an embryo, while the ovule matures into a naked seed.

Angiosperms, the flowering plants, are the most advanced group and produce seeds enclosed in fruits. Their reproductive structures are specialized flowers, which bear both pollen grains and ovules. Angiosperms are the most diverse and widespread plants, ranging from minute Wolffia to towering Eucalyptus trees. They are of immense ecological and economic importance, providing food, medicine, fuel, timber, and other resources. Based on the number of cotyledons, they are classified into dicotyledons (two cotyledons) and monocotyledons (one cotyledon). This group dominates the terrestrial flora and plays a key role in sustaining life on Earth.

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