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After reading this essay you will learn about:- 1. Introduction to Flowering Plants 2. Angiosperm Derived Characteristics of Flowering Plants 3. Flowering Plant Diversity 4. Fruit and Seed of Flowering Plants.
Essay on Flowering Plants
Essay Contents:
- Essay on the Introduction to Flowering Plants
- Essay on the Angiosperm Derived Characteristics of Flowering Plants
- Essay on the Flowering Plant Diversity
- Essay on the Fruit and Seed of Flowering Plants
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1. Essay on the Introduction to Flowering Plants:
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The flowering plants or angiosperms (Angiospermae or Magnoliophyta) are the most diverse group of land plants. The flowering plants and the gymnosperms are the only extant groups of seed plants. The flowering plants are distinguished from other seed plants by a series of apomorphies, or derived characteristics.
The ancestors of flowering plants diverged from gymnosperms around 245-202 million years ago, and the first flowering plants known to exist are from 140 million years ago. They became widespread around 100 million years ago, but replaced conifers as the dominant trees only around 60-100 million years ago.
2. Essay on the Angiosperm Derived Characteristics of Flowering Plants:
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Flowers:
The flowers, which are the reproductive organs of flowering plants, are the most remarkable feature distinguishing them from other seed plants. Flowers aid angiosperms by enabling a wider range of adaptability and broadening the ecological niches open to them. This has allowed flowering plants to largely dominate terrestrial ecosystems.
Stamens with Two Pairs of Pollen Sacs:
Stamens are much lighter than the corresponding organs of gymnosperms and have contributed to the diversification of angiosperms through time with adaptations to specialized pollination syndromes, such as particular pollinators. Stamens have also become modified through time to prevent self-fertilization, which has permitted further diversification, allowing angiosperms eventually to fill more niches.
Reduced Male Parts, Three Cells:
The male gametophyte in angiosperms is significantly reduced in size compared to those of gymnosperm seed plants. The smaller pollen decreases the time from pollination — the pollen grain reaching the female plant — to fertilization of the ovary; in gymnosperms fertilization can occur up to a year after pollination, while in angiosperms the fertilization begins very soon after pollination. The shorter time leads to angiosperm plants setting seeds sooner and faster than gymnosperms, which is a distinct evolutionary advantage.
Closed carpel enclosing the ovules (carpel or carpels and accessory parts may become the fruit).
The closed carpel of angiosperms also allows adaptations to specialized pollination syndromes and controls. This helps to prevent self-fertilization, thereby maintaining increased diversity. Once the ovary is fertilized, the carpel and some surrounding tissues develop into a fruit. This fruit often serves as an attractant to seed-dispersing animals. The resulting cooperative relationship presents another advantage to angiosperms in the process of dispersal.
Reduced Female Gametophyte, Seven Cells with Eight Nuclei:
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The reduced female gametophyte, like the reduced male gametophyte, may be an adaptation allowing for more rapid seed set, eventually leading to such flowering plant adaptations as annual herbaceous life cycles, allowing the flowering plants to fill even more niches.
Endosperm:
Endosperm formation generally begins after fertilization and before the first division of the zygote. Endosperm is a highly nutritive tissue that can provide food for the developing embryo, the cotyledons, and sometimes for the seedling when it first appears.
These distinguishing characteristics taken together have made the angiosperms the most diverse and numerous land plants and the most commercially important group to humans. The major exception to the dominance of terrestrial ecosystems by flowering plants is the coniferous forest.
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Land plants have existed for about 425 million years. Early land plants reproduced sexually with flagellated, swimming sperm, like the green algae from which they evolved. An adaptation to terrestrialization was the development of upright meiosporangia for dispersal by spores to new habitats. This feature is lacking in the descendants of their nearest algal relatives, the Charophycean green algae.
A later terrestrial adaptation took place with retention of the delicate, a vascular sexual stage, the gametophyte, within the tissues of the vascular sporophyte. This occurred by spore germination within sporangia rather than spore release, as in non-seed plants. A current example of how this might have happened can be seen in the precocious spore germination in Sellaginella, the spike-moss.
The result for the ancestors of angiosperms was enclosing them in a case, the seed. The first seed bearing plants, like the ginkgo, and conifers (such as pines and firs), did not produce flowers. Interestingly, the pollen grains (males) of Ginkgo and cycads produce a pair of flagellated, mobile sperm cells that ‘swim’ down the developing pollen tube to the female and her eggs.
The apparently sudden appearance of relatively modern flowers in the fossil record posed such a problem for the theory of evolution that it was called an ‘abominable mystery’ by Charles Darwin. However, the fossil record has grown since the time of Darwin, and recently discovered angiosperm fossils such as Archaefructus, along with further discoveries of fossil gymnosperms, suggest how angiosperm characteristics may have been acquired in a series of steps.
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Several groups of extinct gymnosperms, particularly seed ferns, have been proposed as the ancestors of flowering plants but there is no continuous fossil evidence showing exactly how flowers evolved. Some older fossils, such as the upper Triassic Sanmiguelia, have been suggested. Based on current evidence, some propose that the ancestors of the angiosperms diverged from an unknown group of gymnosperms during the late Triassic (245-202 million years ago).
A close relationship between angiosperms and gnetophytes, proposed on the basis of morphological evidence, has more recently been disputed on the basis of molecular evidence that suggest gnetophytes are instead more closely related to other gymnosperms.
The earliest known angiosperm macrofossil, Archaefructus liaoningensis, is dated to about 125 million years BP (the Cretaceous period), while pollen considered to be of angiosperm origin takes the fossil record back to about 130 million years BP. There is, however, circumstantial chemical evidence for the existence of angiosperms as early as 250 million years ago.
Oleanane, a secondary metabolite produced by many flowering plants, has been found in Permian deposits of that age together with fossils of gigantopterids Gigantopterids are a group of extinct seed plants that share many morphological traits with flowering plants, although they are not known to have been flowering plants themselves.
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Recent DNA analysis (molecular systematics) show that Amborella trichopoda, found on the Pacific island of New Caledonia, belongs to a sister group of the other flowering plants, and morphological studies suggest that it has features that may have been characteristic of the earliest flowering plants.
The great angiosperm radiation, when a great diversity of angiosperms appears in the fossil record, occurred in the mid-Cretaceous (approximately 100 million years ago). However, a study in 2007 estimated that the division of the five most recent (the genus Ceratophyllum, the family Chloranthaceae, the eudicots, the magnoliids, and the monocots) of the eight main groups occurred around 140 million years ago.
By the late Cretaceous, angiosperms appear to have dominated environments formerly occupied by ferns and cycadophytes, but large canopy-forming trees replaced conifers as the dominant trees only close to the end of the Cretaceous 65 million years ago or even later, at the beginning of the Tertiary.
The radiation of herbaceous angiosperm occurred much later. Yet, many fossil plants recognizable as belonging to modern families (including beech, oak, maple, and magnolia) appeared already at late Cretaceous.
It is generally assumed that the function of flowers, from the start, was to involve mobile animals in their reproduction processes. That is, pollen can be scattered even if the flower is not brightly colored or oddly shaped in a way that attracts animals; however, by expending the energy required to create such traits, angiosperms can enlist the aid of animals and thus reproduce more efficiently.
Island genetics provides one proposed explanation for the sudden, fully developed appearance of flowering plants. Island genetics is believed to be a common source of speciation in general, especially when it comes to radical adaptations that seem to have required inferior transitional forms.
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Flowering plants may have evolved in an isolated setting like an island or island chain, where the plants bearing them were able to develop a highly specialized relationship with some specific animal (a wasp, for example).
Such a relationship, with a hypothetical wasp carrying pollen from one plant to another much the way fig wasps do today, could result in both the plant(s) and their partners developing a high degree of specialization. Note that the wasp example is not incidental; bees, which apparently evolved specifically due to mutualistic plant relationships, are descended from wasps.
Animals are also involved in the distribution of seeds. Fruit, which is formed by the enlargement of flower parts, is frequently a seed-dispersal tool that attracts animals to eat or otherwise disturb it, incidentally scattering the seeds it contains. While many such mutualistic relationships remain too fragile to survive competition and spread widely, flowering proved to be an unusually effective means of reproduction, spreading (whatever its origin) to become the dominant form of land plant life.
Flower ontogeny uses a combination of genes normally responsible for forming new shoots The most primitive flowers are thought to have had a variable number of flower parts, often separate from (but in contact with) each other.
The flowers would have tended to grow in a spiral pattern, to be bisexual (in plants, this means both male and female parts on the same flower), and to be dominated by the ovary (female part). As flowers grew more advanced, some variations developed parts fused together, with a much more specific number and design, and with either specific sexes per flower or plant, or at least ‘ovary inferior’.
Flower evolution continues to the present day; modern flowers have been so profoundly influenced by humans that some of them cannot be pollinated in nature. Many modern, domesticated flowers used to be simple weeds, which only sprouted when the ground was disturbed.
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Some of them tended to grow with human crops, perhaps already having symbiotic companion plant relationships with them, and the prettiest did not get plucked because of their beauty, developing a dependence upon and special adaptation to human affection.
The botanical term ‘Angiosperm’, from the Ancient Greek, angeion (receptacle, vessel) and, (seed), was coined in the form Angiospermae by Paul Hermann in 1690, as the name of that one of his primary divisions of the plant kingdom.
This included flowering plants possessing seeds enclosed in capsules, distinguished from his Gymnospermae, or flowering plants with achenial or schizo-carpic fruits, the whole fruit or each of its pieces being here regarded as a seed and naked. The term and its antonym were maintained by Carolus Linnaeus with the same sense, but with restricted application, in the names of the orders of his class Didynamia.
Its use with any approach to its modern scope only became possible after 1827, when Robert Brown established the existence of truly naked ovules in the Cycadeae and Coniferae, and applied to them the name Gymnosperms. From that time onwards, so long as these Gymnosperms were, as was usual, reckoned as dicotyledonous flowering plants, the term Angiosperm was used antithetically by botanical writers, with varying scope, as a group-name for other dicotyledonous plants.
In 1851, Hofmeister discovered the changes occurring in the embryo-sac of flowering plants, and determined the correct relationships of these to the Cryptogamia. This fixed the position of Gymnosperms as a class distinct from Dicotyledons, and the term Angiosperm then gradually came to be accepted as the suitable designation for the whole of the flowering plants other than Gymnosperms, including the classes of Dicotyledons and Monocotyledons. This is the sense in which the term is used today.
In most taxonomies, the flowering plants are treated as a coherent group. The most popular descriptive name has been Angiospermae (Angiosperms), with Anthophyta (‘flowering plants’) a second choice. These names are not linked to any rank. The Wettstein system and the Engler system use the name Angiospermae, at the assigned rank of subdivision.
The Reveal system treated flowering plants as subdivision Magnoliophytina, but later split it to Magnoliopsida, Liliopsida and Rosopsida. The Takhtajan system and Cronquist system treat this group at the rank of division, leading to the name Magnoliophyta (from the family name Magnoliaceae).
The Dahlgren system and Thorne system (1992) treat this group at the rank of class, leading to the name Magnoliopsida. However, the APG system, of 1998, and the APG II system, of 2003, do not treat it as a formal taxon but rather treat it as a clade without a formal botanical name and use the name angiosperms for this clade.
The internal classification of this group has undergone considerable revision. The Cronquist system, proposed by Arthur Cronquist in 1968 and published in its full form in 1981, is still widely used, but is no longer believed to accurately reflect phylogeny.
A general consensus about how the flowering plants should be arranged has recently begun to emerge, through the work of the Angiosperm Phylogeny Group, who published an influential reclassification of the angiosperms in 1998. An update incorporating more recent research was published as APG II in 2003.
Recent studies, as by the APG, show that the monocots form holophyletic or monophyletic group; this clade is given the name monocots. However, the dicots are not (they are a paraphyletic group). Nevertheless, within the dicots a monophyletic group does exist, called the eudicots or tricolpates, and including most of the dicots. The name tricolpates derives from a type of pollen found widely within this group.
The name eudicots is formed combining dicot with the prefix eu- (from Greek, for ‘well’, or ‘good’, botanically indicating ‘true’), as the eudicots share the characters traditionally attributed to the dicots, such as flowers with four or five parts (four or five petals, four or five sepals).
Separating this group of eudicots from the rest of the (former) dicots leaves a remainder, which sometimes are called informally palaeodicots (Greek prefix ‘palaeo-‘means ‘old’). As this remnant group is not monophyletic this is a term of convenience only.
3. Essay on the Flowering Plant Diversity:
The number of species of flowering plants is estimated to be in the range of 250,000 to 400,000. The number of families in APG (1998) was 462. In APG II (2003) it is not settled; at maximum it is 457, but within this number there are 55 optional segregates, so that the minimum number of families in this system is 402.
The diversity of flowering plants is not evenly distributed. Nearly all species belong to the eudicot (75%), monocot (23%) and magnoliid (2%) clades. The remaining 5 clades contain a little over 250 species in total, i.e., less than 0.1 per cent of flowering plant diversity, divided among 9 families.
The amount and complexity of tissue-formation in flowering plants exceeds that of Gymnosperms. The vascular bundles of the stem are arranged such that the xylem and phloem form concentric rings.
In the Dicotyledons, the bundles in the very young stem are arranged in an open ring, separating a central pith from an outer cortex. In each bundle, separating the xylem and phloem, is a layer of meristem or active formative tissue known as cambium. By the formation of a layer of cambium between the bundles (inter-fascicular cambium) a complete ring is formed, and a regular periodical increase in thickness results from the development of xylem on the inside and phloem on the outside.
The soft phloem becomes crushed, but the hard wood persists and forms the bulk of the stem and branches of the woody perennial. Owing to differences in the character of the elements produced at the beginning and end of the season, the wood is marked out in transverse section into concentric rings, one for each season of growth, called annual rings.
Among the Monocotyledons, the bundles are more numerous in the young stem and are scattered through the ground tissue. They contain no cambium and once formed the stem increases in diameter only in exceptional cases.
Traditionally, the flowering plants are divided into two groups, which in the Cronquist system are called Magnoliopsida (at the rank of class, formed from the family name Magnoliacae) and Liliopsida (at the rank of class, formed from the family name Liliaceae).
Other descriptive names allowed by Article 16 of the ICBN include Dicotyledones or Dicotyledoneae, and Monocotyledones or Monocotyledoneae, which have a long history of use. In English a member of either group may be called a dicotyledon (plural dicotyledons) and monocotyledon (plural monocotyledons), or abbreviated, as dicot (plural dicots) and monocot (plural monocots).
These names derive from the observation that the dicots most often have two cotyledons, or embryonic leaves, within each seed. The monocots usually have only one, but the rule is not absolute either way. From a diagnostic point of view the number of cotyledons is neither a particularly handy nor reliable character.
The characteristic feature of angiosperms is the flower. Flowers show remarkable variation in form and elaboration, and provide the most trustworthy external characteristics for establishing relationships among angiosperm species. The function of the flower is to ensure fertilization of the ovule and development of fruit containing seeds. The floral apparatus may arise terminally on a shoot or from the axil of a leaf (where the petiole attaches to the stem).
Occasionally, as in violets, a flower arises singly in the axil of an ordinary foliage-leaf. More typically, the flower-bearing portion of the plant is sharply distinguished from the foliage- bearing or vegetative portion, and forms a more or less elaborate branch-system called an inflorescence.
The reproductive cells produced by flowers are of two kinds. Microspores, which will divide to become pollen grains, are the ‘male’ cells and are borne in the stamens (or microsporophylls). The ‘female’ cells called megaspores, which will divide to become the egg-cell (megagameto- genesis), are contained in the ovule and enclosed in the carpel (or megasporophyll).
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The flower may consist only of these parts, as in willow, where each flower comprises only a few stamens or two carpels. Usually other structures are present and serve to protect the sporophylls and to form an envelope attractive to pollinators. The individual members of these surrounding structures are known as sepals and petals (or tepals in flowers such as Magnolia where sepals and petals are not distinguishable from each other).
The outer series (calyx of sepals) is usually green and leaf-like, and functions to protect the rest of the flower, especially the bud. The inner series (corolla of petals) is generally white or brightly coloured, and is more delicate in structure. It functions to attract insect or bird pollinators.
Attraction is effected by colour, scent, and nectar, which may be secreted in some part of the flower. The characteristics that attract pollinators account for the popularity of flowers and flowering plants among humans.
While the majority of flowers are perfect or hermaphrodite (having both male and female parts in the same flower structure), flowering plants have developed numerous morphological and physiological mechanisms to reduce or prevent self-fertilization.
Heteromorphic flowers have short carpels and long stamens, or vice versa, so animal pollinators cannot easily transfer pollen to the pistil (receptive part of the carpel). Homomorphic flowers may employ a biochemical (physiological) mechanism called self- incompatibility to discriminate between self-and non-self-pollen grains. In other species, the male and female parts are morphologically separated, developing on different flowers.
Double fertilization refers to a process in which two sperm cells fertilize cells in the ovary. This process begins when a pollen grain adheres to the stigma of the pistil (female reproductive structure), germinates, and grows a long pollen tube. While this pollen tube is growing, a haploid generative cell travels down the tube behind the tube nucleus.
The generative cell divides by mitosis to produce two haploid (n) sperm cells. As the pollen tube grows, it makes its way from the stigma, down the style and into the ovary. Here the pollen tube reaches the micropyle of the ovule and digests its way into one of the synergids, releasing its contents (which include the sperm cells).
The synergid that the cells were released into degenerates and one sperm makes its way to fertilize the egg cell, producing a diploid (2n) zygote. The second sperm cell fuses with both central cell nuclei, producing a triploid (3n) cell. As the zygote develops into an embryo, the triploid cell develops into the endosperm, which serves as the embryo’s food supply. The ovary now will develop into fruit and the ovule will develop into seed.
4. Essay on the Fruit and Seed of Flowering Plants:
As the development of embryo and endosperm proceeds within the embryo-sac, the sac wall enlarges and combines with the nucellus (which is likewise enlarging) and the integument to form the seed-coat. The ovary wall develops to form the fruit or pericarp, whose form is closely associated with the manner of distribution of the seed.
The character of the seed-coat bears a definite relation to that of the fruit. They protect the embryo and aid in dissemination; they may also directly promote germination. Among plants with indehiscent fruits, the fruit generally provides protection for the embryo and secures dissemination. In this case, the seed-coat is only slightly developed. If the fruit is dehiscent and the seed is exposed, the seed-coat is generally well developed, and must discharge the functions otherwise executed by the fruit.
Agriculture is almost entirely dependent on angiosperms, either directly or indirectly through livestock feed. Of all the families plants, the Poaceae, or grass family, is by far the most important, providing the bulk of all feed stocks (rice, corn – maize, wheat, barley, rye, oats, pearl millet, sugar cane, sorghum). The Fabaceae, or legume family, comes in second place.
Also of high importance are the Solanaceae, or nightshade family (potatoes, tomatoes, and peppers, among others), the Cucurbitaceae, or gourd family (also including pumpkins and melons), the Brassicaceae, or mustard plant family (including rapeseed and cabbage), and the Apiaceae, or parsley family. Many of our fruits come from the Rutaceae, or rue family, and the Rosaceae, or rose family (including apples, pears, cherries, apricots, plums, etc.).
In some parts of the world, certain single species assume paramount importance because of their variety of uses, for example the coconut (Cocos nucifera) on Pacific atolls, and the olive (Olea europaea) in the Mediterranean region.
Flowering plants also provide economic resources in the form of wood, paper, fiber (cotton, flax, and hemp, among others), medicines (digitalis, camphor), decorative and landscaping plants, and many other uses. The main area in which they are surpassed by other plants is timber production.
