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How does pollination and fertilization take place in flowering plants? What does flowering plants develop from the ovary wall? The structure and classification of plant fruits. The spread of seeds and their significance in nature and human life

Septa in the ovary, formed as a result of accretion of the lateral surfaces of two carpels (for example, in representatives of the genus Liliura).

  • - Cm....

    Microbiology Dictionary

  • - separate nests of the ovary, communicating with each other ...

    Dictionary of botanical terms

  • - outgrowths of tissues of the inner wall of the ovary, not containing ovules ...

    Dictionary of botanical terms

  • - Synonyms: ovary chambers one or more cavities in the ovary resulting from different options accretion of carpels; in G. z. ovules are found ...
  • - see ovary nests ...

    Plant anatomy and morphology

  • - the time interval between two successive culminations of the same name of the center of the visible disk of the Sun on the same geographic meridian ...

    Astronomical Dictionary

  • - on the wing of the aircraft - plates mounted vertically on the swept wing parallel to the plane of symmetry of the aircraft ...

    Encyclopedia of technology

  • - see evanemohores ...

    Dictionary of botanical terms

  • - see Diggers ...

    Soviet Historical Encyclopedia

  • - underdeveloped tubular epithelial passages that form a network under the serous membrane and in the submucosal layer of the gallbladder wall, as well as in the connective tissue on the surface of the liver ...

    Comprehensive Medical Dictionary

  • - see the List of anat. terms ...

    Comprehensive Medical Dictionary

  • - ed. mouth term used to define clays as mixtures of kaolinite, halloysite, pyrophyllite, montmorillonite, nontronite ...

    Geological encyclopedia

  • - the time interval between two successive lower climaxes of the Sun. The beginning of S.I. is the moment of the lower culmination of the Sun ...

    Marine vocabulary

  • - the self-name of the Diggers, representatives of the extreme left wing of the democratic trend in the English Revolution of the 17th century ...

    Great Soviet Encyclopedia

  • - "" is the self-name of the diggers ...

    Big encyclopedic dictionary

  • - set to delimit, limit. Wed Science, based on the pure benefits of knowledge, rejects all egoistic partitions and equally threatens with its rays all who want to serve it ... A. Ѳ ...

    Michelson's Explanatory Phraseological Dictionary (original orph.)

"TRUE PARTITIONS IN A LINK" in books

Partitions

From the book Living Room the author Zhalpanova Linisa Zhuvanovna

Partitions When planning a living room, you may want to divide the room into several parts using partitions of various designs. Partitions are lightweight walls resting on floors and separating inner space rooms for separate

Partitions made of wood

From the book Living Room the author Zhalpanova Linisa Zhuvanovna

Partitions made of wood The simplest of the wooden partitions are partitions in one plank. They are made of unplaned boards with a thickness of about 5 cm (it is best to choose wide boards, not narrow ones), and are fixed at the bottom on both sides with a plinth, and at the top with

Cinder block partitions

From the book Living Room the author Zhalpanova Linisa Zhuvanovna

Cinder block partitions Cinder block partitions are usually installed in cinder block houses. They consist of blocks measuring 45 x 30 x 7 cm.To make such blocks, you need a mold into which you need to pour cinder concrete (for 100 liters of slag 7 kg of cement (M350), 5 kg

Plaster partitions

From the book Living Room the author Zhalpanova Linisa Zhuvanovna

Gypsum partitions For the construction of partitions, you can take both slabs consisting of one gypsum and slabs with fillers in the form of slag, sawdust, etc. But in any case, carefully dried slabs must be used. Their width can be from 30 to 50 cm, length from 80 to 150 cm, and

PARTITIONS

From the book Plasterboard structures: arches, ceilings, partitions the author Antonov Igor Viktorovich

PARTITIONS The layout of apartments in old buildings does not always satisfy the needs of the owners. Technologies existing today make it possible to easily change the layout of premises, dividing one large one into separately used zones using

Partitions

From book Plasterboard works... Secrets of the master author Nikitko Ivan

Partitions Visually, drywall partitions can be transparent or deaf. Glass or stained glass can be inserted into the frame of the transparent partition, wood, plywood or drywall can be inserted into the deaf frame. The basis of any partition, that is, the frame, can be aluminum,

Partitions

From the book Carpentry Master's Handbook the author Serikova Galina Alekseevna

Partitions Only dry wood is suitable for wooden partitions. When finished, their thickness should be at least 50–100 mm. Partitions made of wood rest on the logs from below and run along the beams from above. The material for them is an edged board with a thickness of 40-50 mm,

Eggplant ovaries fall off, fruits are poorly tied. What to do?

the author

Eggplant ovaries fall off, fruits are poorly tied. What to do? A very common problem for greenhouse grown eggplants. Do not be lazy and pollinate the eggplants by hand or immediately when the first buds appear, spray with the preparation "Bud", "Ovary" or

From the book 1001 answers to important questions of the gardener and the gardener the author Kizima Galina Alexandrovna

Why are the ovaries not growing? Zelentsy often stop growing in cold weather, especially on cold nights. Sometimes this happens when there is a lack of moisture in the soil and air. If the ovaries turn yellow, do not develop, dry up and then fall off, then fertilization has not occurred -

Why do ovaries and even buds fall off in tomatoes and peppers?

From the book 1001 answers to important questions of the gardener and the gardener the author Kizima Galina Alexandrovna

Why do ovaries and even buds fall off in tomatoes and peppers? This can be caused by a lack of nutrition or moisture in the soil, or excessive doses of nitrogen in the initial stage of budding. Plants should not be watered after transplanting until the first infusion appears.

PARTITIONS

From the book How to Build a Country House the author Shepelev Alexander Mikhailovich

PARTITIONS Partitions can be interroom at least 20 cm thick and interroom - at least 10 cm thick. Both are usually made of durable low-combustible, low-, heat- and sound-conducting materials. Wooden partitions are usually plastered.

Partitions

From the book Drywall: Step by Step the author Pustovoitov Vadim Nikolaevich

Partitions Steel perforated profiles (posts and purlins) used in plasterboard mounting kits are an excellent base material for construction interior partitions which can have single or double frame(fig. 42). V

Partitions

From the book Building a house quickly and cheaply the author Simonov Evgeny Vitalievich

Partitions Partitions are lightweight walls that divide the space inside the house into separate rooms and functional areas. If the main walls rest directly on the foundation, then the partitions - on the logs. For partitions, various

Chapter 11 Neighbors in the Flesh, True Enemies, and True Friends of a Christian

From the book Modern Practice of Orthodox Piety. Volume 2 the author Pestov Nikolay Evgrafovich

Chapter 11 Neighbors in the flesh, true enemies and true friends of a Christian For whoever does the will of My Heavenly Father is my brother and sister and mother. Mt. 12, 50 Honor your father and mother. Mt. 15, 4 But if someone does not care about his own people, and especially about his family, he has denied the faith and worse

Partitions

From the author's book

Partitions In order to divide the entire space of the house into separate rooms, partitions are installed. They can be single, double or triple, with or without soundproofing. For device single partitions use unplaned

Flowering plants are a large and diverse group that dominate most terrestrial ecosystems. Its existence depends on the main flowering plants cultivated by man. But to flowering plants appeared, they must go through the stage of pollination and fertilization. How this happens, read this article.

Pollination

This process is carried out by transferring pollen from the stamens to the pistil. How does pollination and fertilization take place in flowering plants? This is done in two ways: self-pollination and cross-pollination. In the first case, the transfer of pollen grains to the pistil occurs in the same flower. This is how peas or tulips are pollinated. With cross-pollination, the pollen of a flower from one plant is transferred to the pistil of another. most often by insects, in rare cases - by wind (sedge and birch), birds and water.

As a result of insect pollination, bright, well-visible flowers with a pleasant smell and nectaries are formed, which produce a sweet liquid. Such plants also produce a lot of pollen. It is food for insects. They are attracted by the bright color or smell of flowers. When insects extract nectar, they touch the surface of the pollen grains, which adhere to their body, and when flying to a flower of another plant, they remain on the pistil. This is how insect pollination takes place. Many are pollinated only by certain insects: scented tobacco - night butterfly, creeping clover is a bee, and meadow clover is a bumblebee.

Cross-pollinated plants are better adapted to changing environmental conditions. But the pollination process in this case depends on a number of factors. And self-pollination does not depend on anything. For him, the weather conditions and the absence of intermediaries are not scary.

Fertilization

A grain of pollen, falling on the stigma of the pistil, begins to germinate gradually. The development of a long pollen tube occurs from the vegetative cell. Growing up, it reaches the level of the ovary, and then the ovule. At the same time, a pair of sperm is formed, which penetrates the pollen tube. It, in turn, enters the ovule through the pollen duct. Then the tube at the very tip breaks and releases the male sperm, which are immediately sent to the embryonic membrane, it is called a sac. This is where the eggs develop.

Further, the fertilization of the egg with one sperm takes place, and the formation of a zygote, from which a small embryo of a completely new organism of plant origin begins to form. At the same time, the fusion of the second sperm occurs with the nucleus of the zygote or with the polar nuclei. As a result, a triploid cell is formed, from which the endosperm arises. It is called a nutrient tissue, which contains reserves of essential substances for the normal development of the embryo of a future plant. This is how the organs of sexual reproduction of flowering plants are represented.

When one sperm with an egg, and the other, with the polar nuclei, merge together, this process is called It is peculiar only to flowering and is a unique feature of angiosperms. A fertilized ovule grows into a seed. As a result, the pistil ovary grows. In flowering plants, a fruit develops from the wall of the ovary.

Reproduction

Any plant, reaching a certain size and passing the appropriate stages of development, begins to reproduce organisms of a similar species. This is reproduction, which is a necessary property of life. All organisms thus prolong the existence of the species itself. Distinguish between sexual and which occurs with the participation of one individual. When plants develop specialized cells - spores, organisms begin to multiply.

Moss, algae, ferns, moss and horsetails. Spores are special small cells with a nucleus and cytoplasm that are covered with a membrane. They are able to endure bad conditions for a long time. But, getting into a favorable environment, they quickly germinate and begin to form daughter plants, the properties of which do not differ from those of the mother.

During sexual reproduction, female and male germ cells merge, resulting in the formation of daughter organisms that are qualitatively different from the parental ones. The parental organisms of the female and male principles are already taking part here.

As part of the ovule, the dominant role is played by macrosporangium. It is in it that the laying of one mother cell takes place, from which macrospores are formed. Three pieces start to die off and eventually collapse. The fourth macrospore - feminine, lengthens and its core divides. Then the daughter nuclei move to different poles of the elongated cell. Each formed nucleus is further divided twice.

Cells located near different poles have four nuclei. This is called the embryo sac, which contains eight haploid nuclei. Further, from each quartet of nuclei, one of them follows to the center of the embryonic sac. There they merge, as a result of which they form a secondary nucleus - diploid.

Then, in the embryo sac, in the cytoplasm, partitions are formed between the nuclei on cellular level... There are seven cells in the bag. Near one of its poles is the egg apparatus, which includes a large egg and two auxiliary cells. At the other pole there are antipode cells, there are three of them in total. So, there are now six in the bag and one is diploid, with a secondary nucleus. It is located in the center of the embryonic sac.

What is an ovary?

It is called the lower thickened part of the pistil with a closed cavity inside, in which the ovules are located. Pollen enters the ovule from the stigma of the pistil, which is protected from unfavorable conditions by an internal moist cavity. In the ovule, the development of female germ cells - ovules - takes place.

fruit with seeds. The ovary of flowers is multi-celled and unilocular. In the first case, it is divided into nests by partitions, and in the second, it is not. The ovary of flowering plants is also divided into single-seeded and multi-seeded. It depends on the number of ovules in it: the plum, for example, has one, and the poppy has many.

What are the types of ovaries?

The types of ovaries of flowering plants are:

  • Upper. It attaches to the receptacle freely, without merging with other sections in the flower. The walls of the ovary are formed from carpels. In flowering plants, a fruit develops from the wall of the ovary. Examples are buttercups and cereals. These flowers are called sub-pest or para-pest.
  • The lower ovary is always under the receptacle. It is formed with the participation of other parts of the flower: the base of sepals and stamens with petals, which in many flowers are attached to the top of the ovary. In flowering plants, fruit develops from the wall of the ovary. Examples are Compositae, cactus and orchid plants. The flower is called supra-pistillate.

  • Semi-inferior ovary. Its top does not grow together with other parts, so it is free. Flowers of this type are called semi-adipose flowers. These are the types of ovaries of flowering plants.

Flowering plants

They are the most progressive group of plants, numbering two hundred and fifty thousand species, distributed throughout the planet Earth. The smallest plant is the duckweed, the diameter of which is equal to one millimeter. She lives in the water. The largest flowering plants are trees that grow to a height of one hundred meters or more.

The emergence of flowering plants occurs due to the development of a special reproductive organ - a flower. In some plants, it is painted in bright colors, in others it smells wonderful. Flowers are small and inconspicuous in plants that look like grass. Despite the huge variety of flowering plants, they all harmoniously fit into our life: they decorate gardens and parks, give the joy of communication with them.

Flower structure

The flower is a complex organ system that ensures the propagation of plants by seeds. Its appearance led to the widespread distribution of angiosperms (flowering) plants on Earth. The flower has many functions. With its participation, stamens with pollen grains, pistils with ovules are formed. It plays a major role in pollination, fertilization, seed and fruit formation.

The flower is a shortened, modified, limited growth shoot bearing the perianth, pistils and stamens. All have flowers that are similar in structure and different in shape. This is how the adaptation to pollination occurs. different ways.

The flower can end in the main or lateral stems, the bare part of which under the flower itself is called the pedicel. It is greatly shortened or completely absent in sessile flowers. The peduncle passes into a receptacle, which is elongated, convex, concave or flat. All parts of the flower are placed on it. These are sepals with petals, stamens with a pistil, in the lower part of which an ovary is formed, in which ovules or ovules are located. A flower with such an ovary has a concave receptacle. If the ovary forms at the top of the pistil, the receptacle will be convex or flat.

The pistil occupies the apical position in the flower. It consists of an ovary, a column and a stigma. Ovules form and develop in the ovary. With the help of the column, the stigma takes the position most favorable for the ingress of pollen, the pollen tube grows along the column.

The pistil is a hollow organ. It is formed from the fusion of the edges of a carpel or several carpels (carpella).

Ovary- the lower part of the pistil, which forms the fruit after pollination. The ovary cavity may contain one or several nests. The walls of the ovary, external and internal, are covered with epidermis. Stomata in the epidermis are few in number, although they can be on both sides of the ovary, external and internal. The cuticle develops mainly on outside... The walls of the ovary are mesophyll. Its cells are poorly specialized, retain their embryonic character, which explains the significant growth of the ovary after fertilization. Both the mesophyll and the epidermis of the ovary walls contain chloroplasts. After fertilization, the ovary develops into a fetus, and the structure of its walls changes significantly.

Stigma- a specialized part of the carpel that receives pollen. The surface of the stigma is covered with a conductive tissue, which often continues into the canal of the column. Conductive tissue is formed from the proliferation of cells of the epidermis and cells of the subepidermal layer. She performs a secretory role. Its cells are relatively large, thin-walled, rich in protoplasm and nutrients. The conductive tissue creates an environment conducive to pollen germination and pollen tube development.

Column in different plants developed in varying degrees, for some it is absent. The tissues that make up the column are more differentiated than the tissues that make up the ovary;

Ovules develop on the walls of the ovary. This part of the ovary wall is called the placenta. Conductive bundles are suitable for the placenta. The epidermis and deeper tissues grow in this place. The position of the placentas in the ovary, and, consequently, the position of the ovules has a regular character, constant for certain taxonomic units.

Ovule consists of nucellus and integument. Its development begins with the inception of a small parenchymal tubercle. The growth of this tubercle leads to the development of the central part of the ovule - nucellus... The development of integuments lags somewhat behind - integuments... One or two covers are laid in the form of circular ridges and, growing up, envelop the ovules on all sides of the nucellus. In the upper part, the integument does not close, leaving a gap, or channel, called spermatic or micropyle... Accordingly, this part of the ovule is called micropillary. Its opposite pole represents the base and is called chalazoi... Here the ovule is attached by the seed to the walls of the ovary.

The ovule is called straight (atropic) if the micropyle and the seedle are on the same axis. Reverse (anatropic) ovules are rotated 180 ° in such a way that the micropyle is located near the base of the ovule. The ovule is called semi-bent (hemitropic) if its axis is at right angles to the axis of the ovule. There are two more types of ovules, curved to varying degrees. The most common are anatropic ovules.

Nucellus corresponds morphologically and functionally to the macrosporangium. In some plants, it is a well-developed multicellular tissue, in others it is markedly reduced, sometimes to a few cells. Cytologically, nucellus cells are meristematic in nature, but the ability to divide, i.e. to the formation of spores, here only the mother cell of spores preserves.

The formation of spores proceeds by means of reduction division, therefore, four haploid cells are formed - macrospores. Of these, only one remains and develops - the embryonic sac. Shape and dimensions embryo sac different plants are different, and its position in nucellus is also different.

The development of the embryo sac consists in several successive divisions of its nucleus. In typical cases, an 8-core embryo sac is formed. In this phase of development, the embryonic sac corresponds to the female gametophyte.

The nuclei are distributed in the embryo sac as follows: at the micropilar pole - the ovum and two accompanying nuclei - synergies, on the opposite - three cores - antipodes. Two nuclei, one from each pole, converge in the center and then merge to form the secondary nucleus of the embryo sac. This embryo sac is ready for fertilization.

During fertilization, one of the sperm fuses with the egg, forming a zygote. The second sperm merges with the secondary nucleus of the embryonic sac, and a triploid nucleus is formed. This type of fertilization is called.

The development of the ovule into a seed is accompanied by the transformation of the ovary into a fruit. The fruit represents the final stage in the development of the reproductive sphere of flowering plants. Its function is to form, protect and spread seeds. Usually the fetus develops as a result of fertilization, but in some angiosperms it can form without fertilization - parthenocarpic. Such fruits do not have seeds and are most often found in many cultivated plants (banana, cucumber, tangerine, grapes, etc.).

Many plants are monocarpic since in ontogeny, they form fruits and seeds once and then die. These include all annuals, as well as biennial plants that produce fruits and seeds once only in the second year. Some perennials are also monocarpic tropical plants... For example, American agave can live up to 100 years and die off after flowering and fruit formation. Plants that repeatedly form fruits and seeds during ontogenesis belong to polycarpics... This group includes woody and most perennial herbaceous plants.

The morphological basis of the fruit is the gynoecium, and above all the ovary. Often, other elements of the flower (receptacle, base of stamens, sepals, etc.) take part in the formation of the fruit of plants, especially those with a lower ovary. In this case, sometimes they speak of "false fruits" as opposed to "real" ones, formed only by the ovary. Examples of such fruits are strawberries, in which the juicy part of the fruit is formed from a strongly overgrown receptacle; rose hips and apple trees, in which hypanthium takes part in the formation of the fruit. However, the definition of the concept of "false fruit" is not entirely correct, since all fruits formed by the inferior ovary should fall into this category, thus confusing the classification of fruits.

In the definition of fruits, the following concepts are used: simple, complex, or composite, fractional, jointed fruits. A special type of formations are infertility.

Simple the fruit develops from one pistil formed by apocarpous single-membered (cherry, pea) or coenocarpic gynoecium (poppy, tulip, cockle, wheat).

Complicated, or made the fruit is formed from a flower with an apocarpous polynomial gynoecium, when each pistil turns into a separate fruit (marsh marigold, raspberry, blackberry, magnolia). The individual fruits that make up the composite fruit can be different: nuts, drupes, leaflets. Depending on this, the prefabricated fruits are called polynuts (strawberries), polystyrene (raspberries), and many-leaves (magnolia).

Fractional the fruit develops from a multi-nest ovary of the coenocarpous gynoecium, if each nest of the ovary turns into an independent fruit (mallow). The disintegrating cenocarps are called schizocarps. Their individual lobes are called mericarpies. Malvaceous fruits that break up into open mericarps are called kalachiks. Borage and labiate fruits are coenobia - they consist of four nut-like lobes.

Jointed the fruit breaks up into separate segments according to the transverse constrictions available on them (wild radish, multi-colored vazel, sowing seradella, etc.). In this case, the number of segments does not correspond to the number of nests in the ovary.

Fertility develops from the inflorescence in the event that the ovaries of flowers during the formation of fruits do not give separate fruits, but grow together into one common formation (pineapple, figs, mulberry tree, beets, spinach, etc.).

With the formation of the fetus, the walls of the ovary grow, it is formed pericarp, or pericarp... It accumulates nutrients - proteins, starch, sugars, oils, vitamins, etc. The pericarp protects the seed or seeds contained within the fruit. In most plants, the pericarp is differentiated into 3 layers: exocarp (extracarp), mesocarp (intercarp), endocarp (intracarp). Histologically, they correspond to the layers of the carpel. Exocarp(from the Greek. exo - outside) is a derivative of the outer (external) epidermis and consists of tightly closed cells with thickened outer walls. For example, in cherry or plum fruit it is a thin shiny or waxed outer layer that is easily removable, in citrus fruit it is a yellow or orange glandular layer. In immature fruits, the exocarp have stomata, in ripe fruits they are invisible. Sometimes small lentils develop in it, like, for example, an apple.

Mesocarp(from the Greek mesos - middle) is formed from the carpel mesophyll, usually it is more developed in comparison with the exo- and endocarp. In cherries and plums, the mesocarp is the edible juicy pulp of the fruit, while in citrus fruits it is a loose whitish layer that lies directly under the yellow. The mesocarp can be dry and underdeveloped (pod, pod).

Endocarp(from the Greek endos - internal) is formed from the internal epidermis of the carpel. It can be single-layer or multi-layer. In cherry, plum, and other stone fruit cultures, the endocarp is represented by sclerified tissue, which forms a bone covering the seed. The citrus endocarp is highly modified and forms a juicy main part of the fruit. The ratio of the thickness of the layers of the pericarp in different species is not the same and is associated with the peculiarities of their distribution.

In accordance with the functions, the fruits are extremely diverse in morphological characteristics - size, shape, color, pericarp consistency, methods of opening, the presence of outgrowths, appendages, etc. Structural features of the fruit are most often associated with seed dispersal. Their diversity forms the basis of the simplest and most widely used morphological classification of fruits in practice. It also takes into account some of the features of the anatomical structure: the number of carpels forming a pistil, the number of nests in the ovary, the number of seeds, the method of opening the fruit, and some other signs.

Depending on the consistency of the pericarp, the fruits are divided into juicy and dry. Fruits can contain one seed, like cherry plum, nasturtium, hazel, or be polyspermous like dope, carnation, bellflower, petunia and other plants.

Juicy and dry single-seeded fruits do not open, the seeds are released when the pericarp is destroyed or as a result of germination. Dry polyspermous fruits, as a rule, have devices for opening and releasing the seeds. The fruits are opened after ripening or later.

Opening polyspermous dry fruits differ in the number of carpels and nests in the ovary that formed them, in the position of the ovary in the flower and in the type of gynoecium. These include flyer, bean, pod (pod), box.

Leaflet- this is the most primitive fruit, formed by one carpel, unilocular, opened at the place of fusion of the edges of the carpel (along the abdominal suture). The opened fruit resembles a leaf. Leaflets are single (field larkspur) and combined, or multileaf (peony, swimsuit, marigold, catchment, magnolia).

Bean- unilocular fruit, formed by one carpel; opens with two valves - at the place of fusion of the edges of the carpel (abdominal suture) and along the midrib (dorsal suture). Seeds (sometimes one seed - for example, in clover, sainfoin) are arranged in one row and attached along the ventral suture. Fruits are varied in appearance: straight (peas, beans, caragana, gleditsia), spirally twisted (alfalfa sowing), bubble-shaped (astragalus-flapweed), articulated (seradella sowing, multicolored vasel). The bean fruit is typical for plants from this. Legumes (Fabaceae), Mimosaceae (Mimosaceae), Caesalpiniaceae (Cesalpiniaceae)

Pod and pod- These are fruits that develop from the upper ovary of the paracarpous gynoecium, consisting of two carpels. Opened longitudinally along two seams from bottom to top. Between the valves there is a septum formed by the placenta and dividing the fetus into two nests. Seeds are attached along its edge in one or two rows. Such fruits are typical for cruciferous plants (cabbage, turnip, levkoy, etc.). The pod and the pod differ in the ratio of the length and width of the fruit. If the length exceeds the width by 3-4 or more times, the fruit is called a pod (rapeseed, mustard); if the length is slightly more than or equal to the width - in a pod (yarotka, shepherd's purse, lunar). In the common weed of the wild radish, the pod is segmented: it does not open with the valves, but breaks up into parts along the constrictions.

Boxes Is a group of fruits that unites all varieties of opening fruits that cannot be attributed to the three previous groups. The boll can be unilocular or multi-celled, which most often depends on the number of nests in the ovary, but sometimes it is not associated with this trait. There are various ways to open the boxes. They can be opened with denticles at the top (common cockle, cloves, tar, primrose), holes (poppy), lid (plantain, henbane), valves. The valves can diverge at the place of fusion of carpels - the abdominal suture (violet, St. John's wort, large-flowered foxglove), along the midrib of the carpels - the dorsal suture (lily, iris, tulip, Chinese tea bush). Sometimes the baffles remain connected together in the center, and the flaps move away from them (dope). Celandine has a large long, narrow capsule similar to a pod, it opens with two valves. Occasionally there are boxes that open with a lid (henbane is black, full color).

Non-opening single-seeded dry fruits differ among themselves in such characteristics as the thickness and density of the pericarp, the presence or absence of appendages, etc. Some non-opening fruits are enclosed in a special formation - a plyus, which develops from overgrown bracts, as, for example, in a hazelnut.

Dry, non-opening fruits include a nut (nut), achene, lionfish and caryopsis.

Nut and nut- these are fruits that have a dense woody pericarp, inside which a single seed is freely located. Between themselves, a nut and a nut differ only in size. Fruits of this type are found in buttercups (buttercup), buckwheat (buckwheat, highlander), etc. Close to this group of fruits is the acorn, the base of which is covered with a cup-shaped plyus made of overgrown and lignified bracts. The thorny cupule also covers the nuts of beech and sowing chestnut. Numerous strawberry nuts sit on a fleshy overgrown receptacle, forming a kind of fruit called strawberry, or fraga. Another multi-nut is the rosehip fruit, or cinarodia. He has individual fruits sitting inside a pitcher-shaped juicy hypanthium.

Achene- a fruit that has a softer leathery pericarp in comparison with a nut, which is easily separated from the seed. Achene is formed from two carpels. It is widespread in Compositae (sunflower, cornflower, string, etc.) and valerian. In many Asteraceae, the achene has a crest. Fractional achenes are also called droplet; it consists of two achenes, which, after ripening, separate, but remain suspended on special legs (conductive bundles of the fetal septum).

Lionfish- these are achenes and nuts, equipped with pterygoid appendages. They are found mainly in woody and shrub plants, for example, in elm, ash, alder, birch, among herbaceous plants - in rhubarb; the fractional lionfish is characteristic of the maple.

Caryopsis formed as a result of fusion of the seed coat with a thin pericarp. Formed by two carpels from the upper ovary of the paracarpous gynoecium. It is typical for cereals (wheat, rye, barley, oats, corn, etc.). Caryopsis are naked (rye, wheat) and filmy (barley, oats). Films are floral scales that persist and grow after flowering.

Juicy fruits... This group includes fruits with a more or less juicy fleshy pericarp that surrounds one or many seeds. Juicy fruits are formed from one or more carpels. The fleshy part of such fruits is usually formed by the intercarp, which consists of thin-walled cells with large vacuoles. Juicy fruits are brightly colored due to the presence of anthocyanin pigment in the cell sap (cherry, plum, black nightshade) or as a result of the formation of chromoplasts (mountain ash, rose hips, tomato). They are found in species of a wide variety of families. Juicy fruits include berry, a composite group of berry-like fruits (pumpkin, orange, apple) and drupe.

Berry- a multi-seeded fruit with a juicy pericarp, covered with a thin skin. The berry has a variety different structure(blueberries, cranberries, grapes, gooseberries, currants, tomatoes, eggplant, persimmons, etc.). In some plants, for example, in gooseberries and currants, the juicy part of the berry is formed not by the pericarp, but by the juicy covers of seeds, and the thin pericarp is the cover of the fruit.

The structure of the pomegranate fruit is peculiar: the pericarp forms a leathery cover and film septa of the fruit, developing from the ovary, and the seed coat, which arose from the integuments, is juicy. The fruit has a special name for pomegranate.

Pumpkin- a kind of berry, formed from the lower ovary. Differs in the strong development of vascular bundles in the pericarp and hard, often lignified exocarp. Pumpkin is typical for pumpkin (pumpkin, cucumber, melon, watermelon, loofah, etc.).

Apple- formed from the lower ovary. From the walls of the ovary, only the very core of the fruit is formed. The endocarp becomes relatively tough, leathery and surrounds the nests with seeds freely lying in them. The overgrown bases of the stamens, sepals, petals and receptacle also take part in the formation of the pulp of the fruit. The apple fruit is typical for apple, pear, quince, hawthorn, etc.

Orange- a multi-celled, multi-seeded juicy fruit with a thick leathery colored exocarp rich in essential oils. The juicy part of the fruit is formed by the overgrown hairs of the inner epidermis of the ovary, which turn into juice sacs. Typical for citrus fruits (lemon, tangerine, orange).

Drupe- single-seeded fruit, formed from one carpel. It is characterized by a clear division of the pericarp into 3 parts: leathery thin exocarp; fleshy juicy mesocarp, and lignified endocarp, forming a bone. It is found mainly in Rosaceae (apricot, cherry, blackthorn, etc.). In almonds and coconut palms, a dry drupe is formed; in their fruits, the intercarp of a mature fruit becomes fibrous and dry.

Along with the above morphological classification of fruits, there are morphogenetic classifications that reflect the evolutionary development of this plant formation. Morphogenetic classification primarily solves the theoretical problems of evolutionary morphology, in particular carpology (the science of fruits) and can be used in phylogenetic systematics.

Modern morphogenetic classifications are based mainly on the origin of the fetus from of a certain type gynoecium: apocarpous, syncarpous, lysicarpous, paracarpous, as well as the position of the ovary in the flower - upper or lower. The number of nests in the ovary is also taken into account. The most primitive are the apocarpous fruits, and among the cenocarp fruits are syncarpous.

Taking into account this approach to classification, all morphological types of fruits can be classified from morphogenetic positions. So, boxes are: a) upper syncarpous: lily, onion, tobacco, dope, henbane, snapdragon, etc.; b) lower syncarpous: iris, gladiolus; v) lower paracarpous: in orchids - orchis, two-leaved lyubka, etc.; e) upper lysicarp: in cloves - cockle, starlet; in primroses - loosestrife, primrose. Berries: a) upper syncarpous: with many seeds - grapes, tomato, potatoes, lily of the valley, asparagus, kupena; with one seed - fruit date palm; b) lower syncarpous: cranberries, lingonberries, blueberries, honeysuckle; v) upper paracarpous: capers, melon tree; G) lower paracarpous: currants, gooseberries; e) upper lysicarp: berry blister. The apple belongs to the lower syncarpous fruits, the pumpkin belongs to the lower paracarpous ones. Leaflets, beans are always the upper apocarpies. are formed from the upper ovary of the apocarpous gynoecium. In general, it should be noted that the same morphological types of fruits can develop from different types of gynoecium. This indicates a convergent evolution associated with seed distribution methods. The main trend in the evolution of gynoecium and fruits is associated with a decrease in the number of carpels forming a pistil and seeds forming in a fruit.

FLOWER
angiosperms (Angiospermae), the largest division of the plant kingdom, characterized by specialized reproductive organs that form a flower. Flowering plants have been known since the Jurassic period (about 150 million years ago): already at that time they were quite highly developed and widespread, so their first representatives, undoubtedly, appeared much earlier, possibly on lands exposed after the retreat of the sea. Subsequently, flowering plants conquered the entire planet, strongly displacing the former dominants, in particular ferns and conifers. It is flowering plants that dominate deciduous forests that once occupied significant areas in North America, and in the vast tropical forests of Central and South America, Africa and Asia. This division includes grasses that cover the American prairies and pampas, African savannas and Eurasian steppes, as well as cacti and thorny shrubs of deserts, many underwater and floating grasses of rivers, lakes and seas, moss-like species creeping over rocks and hanging from tree branches. Finally, it is the flowering plants that a person cultivates in the fields, in vegetable gardens and orchards, they are the main decoration of greenhouses and parks.

LIFE CYCLE OF A FLOWER PLANT.
The flower, a structure unique to this part of the plant, contains the reproductive organs that give rise to seeds and fruit: stamens and pistils. A series of divisions of certain cells contained in them (maternal cells of the megaspore and microspores), including the so-called. reduction division (meiosis), leads to the formation of sex cells (gametes) with half the number of chromosomes in each. For fertilization, the male gamete (sperm) from the pollen grain (more precisely, its nucleus) must merge with the female (egg), which is located in the ovule, enclosed in the ovary of the pistil. For this, a pollen tube growing through the pistil is formed. During fertilization, a zygote appears with a normal (double) number of chromosomes for the species. After a series of its divisions, an embryo is formed. The tissues surrounding it differentiate into the outer protective membrane of the seed and the nutritive tissue (endosperm). In parallel, the ovary (sometimes together with adjacent structures) is modified, turning into a fetus. After a dormant period, the seed germinates and the embryo develops into a new plant. The life cycle is complete.


STRUCTURE OF FLOWER PLANTS


Leaves. The bulk of the organic nutrients on earth comes from the leaves of flowering plants. Typically, the leaf consists of a flat leaf blade on a petiole, which is attached at its base to the stem. At the place of attachment there are two leaf-like outgrowths - stipules. However, each of these structures may be absent. The leaf blades of some flowering plants, such as many labiates and crucifers, are sessile, i.e. depart directly from the stem without a petiole; in other species, only their sheaths with plates reduced to filamentous structures (this can be observed in cereals) remain from the leaves. Inside the leaf there are relatively loosely packed cells rich in green pigment - chlorophyll. Photosynthesis takes place in them. At the upper surface of the leaf, these cells are usually elongated and are located side by side perpendicular to the surface: they form the so-called. palisade parenchyma. The underlying cells are less uniform in shape and are separated by the air cells - this is the so-called. spongy parenchyma. Air exchange of the inner leaf tissues with the environment goes through small holes in the single-layer skin (epidermis) covering it: as a result, photosynthetic cells receive carbon dioxide, which is necessary for the formation of organic matter, and get rid of "production waste" - oxygen. The epidermis is usually covered with a waxy bloom (cuticle) on the outside and is relatively impervious to water and gases, and its cells are incapable of photosynthesis. Unfortunately, the leaf loses a lot of water through evaporation, which can sometimes jeopardize the existence of the entire plant. It is supplied with water through a system of internal veins, usually forming a dense branched network. Veins consist of vascular tissue cells that deliver water with mineral salts dissolved in it to photosynthesizing areas and carry organic matter from there to all parts of the plant. Since some cells of this conductive system are thick-walled, the veins simultaneously play the role of the skeleton of the leaf, maintaining it in a straightened state and ensuring the normal supply of all its parts with light and air.
Stem. Through the conductive cells of the stem, water with mineral salts dissolved in it flows from the root to the veins of the leaf, which contain cells of the same type. In a young stem, this aqueduct system (xylem) usually forms a cylinder that begins underground, serving as a rigid support for leaves, flowers and fruits and is capable of thickening and lignifying over time, turning into a powerful multi-meter trunk. Outside the xylem, there is a similar cylinder - phloem, consisting of cells through which organic matter is transported. The phloem also extends into the veins of the leaf. The rest of the stem consists of soft tissue, sometimes photosynthesizing, which often stores excess nutrients. The central part of the stem - the core - can collapse, and then a cavity remains in the stem in its place. Stems with leaves (as well as flowers and fruits that are believed to have descended from leaves) are called shoots.
Root. The root system anchors the plant in the substrate. There are also conductive tissues at the root - closer to the center of the xylem, farther from the center - phloem. Large amounts of storage substances can also accumulate here, so some roots are very large. In addition to supporting and storing, the most important function of the roots is absorption: water with salts dissolved in it must flow from the soil into the shoots and compensate for the costs and losses of the plant. The absorption is carried out by the so-called. root hairs - numerous outgrowths of superficial root cells in a relatively narrow zone near its tip. It is the root hairs that penetrate between the smallest soil particles that provide a huge total absorbing surface of the underground part of the plant. The presence of a conducting, or vascular, system is a characteristic feature of all flowering plants, which in all other respects can vary greatly in their structure. The xylem and phloem in all flowering plants consist, in principle, of the same, more or less equally located elements. Anatomically, flowering plants are closest to conifers, cycads and other gymnosperms; a more distant evolutionary relationship connects them with ferns.

STRUCTURAL TYPES


Herbaceous plants. In appearance, internal structure and the way of life flowering plants vary greatly. Some are annual grasses that die by the beginning of winter or, in the tropics, by the end of the rainy season. Sometimes, even during such a short life, they manage to reach rather large sizes (examples are the well-known sunflower and corn). Some species use other plants as a support, bringing their leaves into the light. For this, for example, many bean ends compound leaves, consisting of several leaf blades (leaflets), turned into tenacious, spirally twisted antennae. Many flowering plants are perennial grasses: their aerial parts die off in unfavorable seasons for growth, but the underground ones remain alive and give new shoots from year to year. Underground organs perennial plants in structure and nature are different. For a gladiolus, for example, this is the so-called. corms - short thickened stem bases with scaly leaf remnants; in potatoes - tubers formed on the lateral branches of the main stem; the sweet potato has overgrown roots; in other species, in particular Iris, violets, wheatgrass, - rhizomes, i.e. long underground stems. Bulbs of hyacinth, onion and daffodil consist of leaves turned into fleshy scales, densely packed in a kidney-like structure on a flattened stem - the bottom. All of these underground formations accumulate nutrients that allow perennial grasses to survive the unfavorable season and give rise to new aerial shoots. Such repositories of concentrated organic matter make our life much easier: a person uses many "root crops" for food (potatoes, onions, carrots, beets, etc.) and multiplies food crops with their help (for example, potatoes - with pieces of tubers from the so-called . "eyes"). Aerial whiskers, or stolons, are similar in origin to rhizomes - modified stems creeping along the ground, capable of rooting and giving rise to new full-fledged plants. This way vegetative propagation can be observed, for example, in strawberries.


SPROUTING BEAN SEED.
a - The seed absorbs water from the soil, an embryonic root and a stalk (hypocotal knee) appear from under the peel. b - The seed coat bursts, the root burrows into the soil. c - The stalk grows upward, pulling out the embryonic leaves (cotyledons) and the bud that has begun to develop. d - The first true leaves unfold above the cotyledons - the seedling turns into a plant capable of independent existence.


LIFE FORMS OF FLOWERING PLANTS. The cactus is a desert plant adapted to water shortages: the fleshy stem is flattened, the leaves are turned into thorns, the root system is powerfully developed. Buttercup is a typical plant living in conditions of guaranteed moisture: the stem, root and leaves are well developed. Tulip is a plant with a fleshy underground stem (bulb) that stores nutrients. Pemphigus is an aquatic insectivorous plant: there are no roots, the leaves float in the water column and carry bubbles that support the stem with flowers in the air and play the role of traps for small aquatic animals that serve as food for the plant.


Insectivorous plants. Of all the flowering plants, probably the most unusual are the so-called. carnivores or carnivores capable of trapping small animals and using them for food. Such species are known in several families, and their trapping devices are different. For example, sundews (Drosera) keep unwary insects with a sticky secretion of many glandular hairs covering the upper surface of their leaves. The victim not only sticks to those hairs that he has already touched, but also forces neighboring hairs to bend down to her, which makes the grip truly dead. In the Venus flytrap (Dionaea), the leaves consist of two halves, which snap sharply when the prey touches the special sensitive hairs on their surface. The edges of the leaves bear denticles sticking upward and, approaching, like a lattice, they separate the victim from the outside world. In the species Sarracenia, Darlingtonia and Nepenthes, the leaf blades are transformed into trapping jugs, inside which the insects are lured by sweet secretions. Downward spines, overlapping scales, etc., do not allow the victim to crawl back out. leaf outgrowths, so that in the end it drowns in the liquid accumulated at the bottom of the trap, sometimes consisting mainly of rainwater. Pemphigus (Utricularia) is an underwater plant, on the submerged leaves of which there are trapping bubbles with a valve that opens only inward: small aquatic animals get into them. At least some of these bubbles secrete juice that digests the victim's proteins. As a result carnivorous plants is probably less dependent than other species on soil inorganic nitrogen for the synthesis of their own proteins.

FLOWERS


Flowering plants reproduce in various ways: they regenerate from separated vegetative parts (cuttings, leaves, their pieces, etc.), form daughter individuals from rhizomes, stolons, roots, bulbs, tubers and similar formations, but the main and unique reproductive organ for this group - a flower, the structure of which, although it varies widely, obeys a principle that is uniform for all species.
Structure. A flower is a specialized shoot or, more likely, a system of shortened and closely spaced shoots, parts of which form several concentric circles or spirals around the top. Outside, there is usually a calyx of green sepals covering other parts of the flower in an unopened bud. As a rule, a corolla of brightly colored and pleasantly scented petals is located closer to the center. Both of these circles form the so-called. perianth. Even closer to the center are the stamens, and, finally, directly in it - one or more pistils. These are the actual reproductive parts of the flower - male and female, respectively. Sometimes the calyx, corolla, entire perianth, stamens or pistils are absent in the flower. For example, a single cereal flower consists of three stamens and one pistil, surrounded by hard scales, which, strictly speaking, cannot be called petals or sepals. Oak trees have two types of flowers: some consist of stamens with sepals, others only of pistils. However, in any case, in order for a flower to take part in reproduction, it must have stamens or pistils; if neither one nor the other is present, it is sterile. However, in some species sterile flowers are used to attract pollinators (for example, marginal "petals" in sunflower inflorescences), and a person specially displays "double" peonies, carnations and other flowering plants without stamens and pistils for decorative purposes.


TYPICAL BULK FLOWER often five-membered: five sepals, petals, stamens and carpels fused into one pistil with a five-lobed stigma. Longitudinal section: pollen grains are visible in the anthers, and ovules (potential seeds) in the ovary.
Pollination. The reproductive part of the stamen is its head, the so-called. anther. It usually consists of four pollen sacs located side by side. When ripe, they open up with longitudinal cracks or rounded pores and release pollen - many tiny, volatile or sticky pollen grains.


Pollination by the wind. Wind-pollinated plants form huge quantities fly pollen: most of it is lost to no use, and only individual pollen grains, accidentally hitting the stigma of a pistil in a flower of a specimen of the same species, provide reproduction. This method of pollination is typical for many trees (not only flowering, but also conifers), grasses, sedges and some well-known weeds, such as wormwood and ragweed. Their fly pollen is capable of causing hay fever, which affects many people. Ambrosia blooming at the end of summer is especially dangerous in this sense. Pollination by insects. Sticky pollen can simply fall from the anther to the pistil, but more often it is carried from flower to flower by insects (sometimes birds and even small mammals also play the role of pollinators). The relationship of flowering plants with the animals visiting their flowers is very interesting, and it is difficult to explain their occurrence without resorting to the concept of "purpose". As a result, you can often hear that insects "look for" well-defined flowers, and those, in turn, "arrange" their stamens in the calculation of this particular guest. Be that as it may, insects are really attracted to pollinated flowers by their color and smell, not necessarily pleasant. Flies, for example, fly to the smell of carrion, spread by kirkazon and "skunk cabbage" (stinking symplocarpus), and moths react to the bright whiteness of species blooming at dusk. Penetrating into the flower for food, the pollinator involuntarily shakes off the pollen grains and some of this pollen can then just "accidentally" leave on the stigma of the pistil of the same or another flower, not necessarily even a flower of the same species. Food for such insects is either the pollen itself, or, in most cases, nectar - a sweet liquid formed by structures of various origins - nectaries and accumulating in the depths of the corolla or in special tubular petals - spurs, for example, in violets and larkspur. Usually, an insect pollinated flower is designed in such a way that you have to get to the nectar by touching the stamens, which in some cases are equipped with special mechanisms that react to such touch. For example, the walls of the anthers can be under pressure, like in Kalmia: as soon as you touch them, they explode and shower the guest with pollen grains. Among these adaptations, the most surprising are those that provide for cross-pollination, i.e. the transfer of pollen to the pistil of a flower, not of the same plant specimen (this is called self-pollination), but of another. Cross-pollination is beneficial in that it increases the diversity of the species, and therefore, the chances of this taxonomic group as a whole, for survival. However, contrary to Darwin's opinion, self-pollination also does not always lead to degradation, and many plants constantly use it. In some, flowers do not open at all, and pollen reaches the pistil without any external carrier. However, cross-pollination seems to be more widespread, even among wind-pollinated species: many of them have flowers either pistillate or staminate (unisexual), and often some plants are purely female, while others are purely male. Flower structure and pollination. In many flowers, the stamens ripen earlier or later than the pistils, so that self-pollination is impossible in them, but the pollen can be transferred to another specimen of the same species, the pistils of which are quite ready to receive it. For example, in sage (Salvia), the anther of each stamen, strongly elongated and curved by a rocker, resembles a lever: climbing into the corolla tube, the insect inevitably presses its head on its short shoulder - the long one falls, touches the insect's back and leaves a portion of pollen on it. In older flowers, the anthers are already empty, but the pistil bends in an arc so that its stigma is just where the pollen-stained back of the pollinator should appear. The tubular flowers of the same primrose species are of two types: in some specimens, the anthers are located above the mouth of the tube, and the stigma of the pistil is in the depth, in others it is vice versa. Crawling head first into the tube for nectar, insects in the first case stain only the back with pollen, and in the second - only the head and then leave pollen, respectively, only on long or only short pistils, i.e. already on other plants. In some violets on the same plant, some flowers are clearly visible, capable only of cross-pollination, while others are small, non-opening - only self-pollination is possible for them; the latter, by the way, are more prolific. The most sophisticated mechanism for cross-pollination occurs in most orchid species. In the center of their flower is the so-called. a column of a single stamen fused with a pistil. The pollen grains are combined into bag-like masses - pollinia. Each of them is located in a special recess and is equipped with a leg, the end of which is connected with a sticky disk (sticky stick). The adherent sticks to the insect that has visited the flower so precisely that the entire mass of pollen can only be on the stigma of the pistil of another flower of the same species.

FERTILIZATION


The most complex part of the flower is the pistil. It consists of one or several carpels, on the walls of which there are seed rudiments - ovules. The ovules are concentrated in the lower swollen part of the pistil, called the ovary, and the upper part forms a more or less extensive and sticky "landing site" for pollen - the stigma. It often rises above the ovary on a rod-shaped column. Once on the stigma, the pollen grain receives water and nutrients from it and grows into a pollen tube, which penetrates the ovary and, ultimately, the ovule. There she breaks through and releases two male gametes. One of them merges with the egg in the ovule - fertilization occurs and a zygote appears, giving rise to a new plant. An embryo develops from the zygote, and from the surrounding tissues a supply of nutrients for it (in many cases it is the endosperm) and a protective membrane - the ovule turns into a seed. Thus, fertilization and seed development takes place inside the ovary. It is to this structure that flowering plants, also called angiosperms, are mainly due to their evolutionary success. The embryo inside the seed can remain dormant for many weeks, months, and even years: it is protected from external influences by the seed coat and supplied with a food supply; at favorable conditions it will begin to grow, at the expense of internal reserves, rapidly increasing in size its rudimentary structures, and will turn into a seedling. This process is called seed germination. The sizes of seeds in flowering plants are very diverse - from microscopic ones in orchids to huge ones in a coconut palm. One plant can form colossal quantities of them: plantain and shepherd's purse - more than five thousand a year, wormwood (Artemisia vulgaris) - more than a million. Some seeds are edible, some are poisonous, some are so hard that you can't cut them with a knife. Their shape and color are very diverse, they are smooth and wrinkled, sticky and hairy. The fact that seeds contain a supply of nutrients is widely used by humans. Wheat flour, castor oil, or, for example, the sugar found in sweet corn kernels, we get all of this from the endosperm of the seeds. In other cases, reserve substances are found inside the embryo itself, in its fleshy edible cotyledons. This, for example, is the case with soybeans, peanuts, beans and peas, the seeds of which are devoid of endosperm.


TYPES OF FLOWERING PLANTS.
In flowering ovaries, two types of ovaries are distinguished: the lower one is, as it were, recessed in the receptacle, and the stamens and perianth are attached above it; the upper one is located above the place of their origin. The type of ovary is a characteristic feature of each plant species and determines the characteristics of the fruit that forms from it. The upper ovary is characteristic, for example, of blackberries, cherries and peaches; lower - iris (iris), sunflowers and orchids.


FRUIT


While the seeds inside the ovary are ripe, it itself also changes and turns, sometimes together with other parts of the flower, into a fruit. Its wall, called the pericarp, can be juicy, dry, consist of layers of different consistency and carry various appendages. The variety of fruits is so great, and their origin and components are so heterogeneous that there is not only a generally accepted classification, but even uniform definition the word "fruit".
Variety of fruits. The fruit of the orange, called hesperidium or pomeranian, and the fruit of the grape, the berry, are formed only from the ovary; cherry fruit - drupe - too. In the latter case, both the juicy edible part and the hard bone are the different layers of the pericarp surrounding the seed. An apple is formed by an ovary immersed in the base of a flower - a receptacle - and fused with it. The juicy part of this fruit corresponds exactly to the receptacle, and the ovary itself is only a leathery "stub". What is commonly called a rosehip fruit is also a receptacle that has grown into a fleshy jug-like structure, inside which there are not seeds (as is commonly believed), but a lot of nuts, comparable in nature to grapes or oranges and containing one seed each. Thus, here we can talk about a complex, or composite, fruit - a multi-root. One carpel is involved in the formation of each rosehip nut, and several carpels are involved in the formation of each apple and orange fruit, which have grown together into one pistil with a multi-nested ovary. The edible part of the "strawberry" also does not correspond to the ovary: this is also an overgrown receptacle, the convex surface of which is covered not with seeds, but with nuts developing from individual carpels with seeds inside. Again we have many nets in front of us. In the raspberry flower, like strawberries, there are many carpels that are not fused with each other, and therefore ovaries. Each of them gives rise to a small juicy drupe, like a cherry, and all together they grow together into a prefabricated, or complex, fruit - a drupe. Raspberry fruits are outwardly very similar to mulberry seedlings: the difference in terminology is explained by the fact that the latter develop from the ovaries of not one flower, but many flowers collected in a compact brush. Pineapple seed fruit is formed in a similar way, but its edible part consists not only of densely packed derivatives of many flowers, but also of the vegetative parts of the inflorescence that have grown together with them and become fleshy. From the inflorescences of burdock and cocklebur, seedlings (polyseeds) are also formed: they are not juicy, but dry, surrounded by leaves of a wrapper with tenacious hooks at the top of each. Many fruits are small and inedible, so in common parlance they are often called "seeds", although in origin they correspond to a whole orange or apple, and not just the seeds inside them. Moreover, each "seed" of, say, a sunflower or dandelion is formed not only by the seeds and ovary, but also by other parts of the small flowers of these plants. In particular, the "parachute" of the dandelion by its nature corresponds to the sepals. Fruit walnut are also heterogeneous in origin: not only the ovary, but also other parts of the flower are involved in their development. As a matter of fact, these are not nuts, but drupes, like those of cherries or peaches, only the outer fleshy part of the fruit dries up when ripe and falls off the stone. These examples demonstrate the difficulties that botanists face when trying to develop a classification of fruits that takes into account not only their final structure, but also the peculiarities of formation. The division of fruits into vegetables and fruits, which is often found in everyday life, has no scientific meaning at all. Moreover, if "fruit" in the conventional sense still corresponds to the fruit, then "vegetables" include not only fruits, but also other edible parts of plants.


TYPES OF FRUIT.
Orange, or hesperidium, is a special type of berry-like fruit characteristic of citrus fruits, in particular oranges; its peel (zest) and juicy pulp are formed from the walls of the ovary. In the apple, the fleshy part is a derivative of the receptacle; an ovary is immersed in it, which forms only the central part of the fruit with seeds. In the drupe of the plum, both the fleshy pulp and the hard bone are formed by the wall of the ovary; the only seed is inside the seed. Raspberries and strawberries have a composite fruit that develops from one flower with many pistils. Figs and pineapples are not eaten with fruits, but with fruit, formed by many densely packed flowers and the surrounding parts of the inflorescence.


Seed. The importance of all the structures described above for the species can be understood only if it is remembered that there is an embryo inside the seed - the rudiment of a new generation. This tiny plant often has to remain dormant for a long time, waiting for conditions favorable for germination. It must have a supply of food in order to quickly pass the initial stages of development, which, in turn, is possible only where competition from plants of its own and other species is not too great. The firm consistency of the seed coat and sometimes the pericarp protects the embryo during dormancy. Some seeds are covered with long hairs, such as those of cotton and wool, which makes them volatile and can be carried long distances by the wind. Others carry elastic outgrowths that allow them to "jump" out of the fetus. The structural features of some fruits also contribute to the dispersal of seeds: pterygoid outgrowths, like in maple and ash, fluffy appendages, like in dandelion and thistle, or hooks clinging to the integuments of animals, like a string or burdock. Juicy fruits are often pecked by birds. Seeds due to their hard shells are not digested in their gastrointestinal tract and fall on the ground with excrement sometimes many kilometers from the parent plant. Even juicy fruits no one eats, they, decomposing, enrich the soil with water and nutrients necessary for the germination of the seeds contained inside.
The embryo. With all the variety of sizes and shapes of seeds of flowering plants, the structure of the embryo in them follows a single principle. At one end of its stem-like axis there is a rudimentary root, at the other - a bud with one or two germinal leaves adjacent to it - cotyledons. The structure of the latter varies widely depending on the species. In legumes, they take up most of the seed and, during its development, absorb nutrients from the endosperm, which eventually disappears. In a walnut, they are very wrinkled and connected by a thin bridge. In cereals, liliaceae, palms, and many other families of the cotyledon, there is only one: sometimes it forms a wide shield that separates the embryo from the endosperm, sometimes it is only a spine protruding above the kidney. The fleshy cotyledons of legumes contain food; the cotyledon-shield of cereals secretes enzymes that digest the endosperm and supply the developing embryo with nutrients. Many cotyledons are flat, leaf-shaped, folded in various ways inside the seed, and after germination, they take the form of typical leaves and for some time perform their functions. Usually the seed dormancy period lasts several months. At this time, inside them, processes often occur, called the "ripening" of the embryo: without them, germination is impossible. In other cases, germination is delayed due to the impermeability of the seed coat. For such seeds to become viable, their surface must be scratched or treated with acid - this is called scarification. Most seeds lose their viability after a few months or years, but in some species they can germinate after a dormant period of more than a thousand years.

GROWTH AND GROWTH


The germination of the seed begins with the entry of water into it: it swells and the seed coat bursts. From under it, the tip of the embryonic root appears, which begins to lengthen rapidly, bending downward under the action of gravity. Lower, i.e. located between the root and the cotyledons, a part of the embryonic peduncle (hypocotyledonous knee) emerges from under the seed coat and the remnants of the endosperm "backwards", pulling the cotyledons along with it. Then the stem straightens and often brings the cotyledons to the surface, where they straighten out and where photosynthesis begins. Sometimes on the cotyledons, scraps of the seed coat are preserved in the form of a cap. At this stage, the seedling is already capable of absorbing water with mineral salts from the soil and carrying out photosynthesis, i.e. becomes independent of other parts of the seed and fruit. Sometimes, however, the cotyledons remain underground, like in peas, and the kidney that receives food from them is the first to start growing. An aerial stem and the first photosynthetic leaves develop from the bud.
Growth types. Plant development includes cell division, cell enlargement and differentiation. On early stages development, all cells of the embryo are almost the same, and the growth of its parts, in particular the root, is mainly due to the first two of these three processes. Cells near the root tip divide and lengthen rapidly, pushing the root tip deeper into the ground. The same type of growth is characteristic of the stem: at its very top, the cells divide more or less continuously, and those of them that are "in the second echelon" increase in size and acquire mature features, while simultaneously pushing the cells of the "first echelon" upward.
Buds and leaves. A bud that has started to grow develops according to the same scheme, but here the matter is complicated by the formation of leaves. They are laid at the apex of the shoot in the form of lateral papillae directed forward. As the stem grows, these leaf buds separate, straighten, enlarge, and differentiate. After that, there are no cells that can continue dividing in the leaves, so the size of the leaves is limited and their lifespan is relatively short. New leaves can appear almost continuously throughout the life of the plant, but in areas with a pronounced change of seasons in perennial plants, the buds periodically fall into a state of dormancy. Growth stops, and specialized outer leaves develop on them, which become tough, close tightly, often stick together and protect the more delicate tissues under them from adverse weather conditions. When the weather allows growth to resume, these bud scales disperse, fall off, and new shoots emerge from under them. Interestingly, all the foliage that covers the trees in spring and summer is usually laid during a short period of the previous year. The kidneys are not only apical. With the elongation of the stem and the maturation of its cells, small groups of cells in the axil of each leaf remain undifferentiated and capable of division: they form lateral, or axillary buds, which can give rise to lateral shoots. As a result, the arrangement of the latter is usually the same as that of the leaves of a given species - alternate, opposite or whorled. Buds can also form from other undifferentiated cells that remain in the mature stem. Such buds, like additional roots called adventitious ones, often appear when the stem is cut off or severely damaged.
Secondary growth. As the stem develops, conducting tissues develop in it - the already mentioned xylem and phloem. Between them, in most flowering plants, there is a so-called. cambium is a layer of undifferentiated cells that continue to divide in the same way as apical cells, i.e. continuously or throughout the growing season. In the course of this division, the cambium deposits more and more layers of conductive tissue: closer to the center - xylem, in the opposite direction - phloem. Every year the wood (formed by the xylem cambium) becomes thicker and thicker. At the same time, in temperate latitudes in spring, cambium lays its widest cells, and in autumn, the narrowest, so the boundaries between layers (annual rings) that have grown in different years are usually clearly visible. By counting the growth rings at the base of the stump, you can determine the age of the tree. Since the thickness of each ring depends on the weather conditions of the year in which it was formed, sometimes it is even possible to judge the recent climate changes from these data. In addition, the study of tree rings sometimes makes it possible to date wood found during archaeological excavations and to determine the age of structures built hundreds of centuries ago. The pattern formed on the cut of the trunk by these rings and the rays of the vascular tissue that cross them, extending into the lateral branches, is called the texture of wood and serves as one of the most important economic signs each forest species. The phloem in trees is never so thick. First, it is replenished with new cells more slowly than xylem. Secondly, their walls remain soft, therefore, after dying off, the protoplasts collapse. In addition, first outside of the phloem, and then in its thickness, and more than once, the so-called. cork cambium, the cells of which, dividing, lay a waterproof cork impregnated with a fat-like substance closer to the surface of the trunk. Since it does not allow water to pass through, all tissues outside of it die off and turn into a hard crust, or outer bark. Mechanically, it is inseparable from the inner cortex, i.e. lying deeper than living cells up to the cambium, and is removed together with them in a single layer. Thus, if the trunk is "debarked", i.e. peeling off the bark from it, the phloem will also be removed; the transport of nutrients will stop and the tree will die. However, to achieve the same result, it is enough to simply cut the bark with a ring, interrupting the phloem communication between the roots and photosynthesizing leaves. This technique of killing trees is called "ringing".

SOCCETES


The flowers of some plant species appear singly - at the ends of the shoots, as, for example, in magnolias (Magnolia). It is believed that such their arrangement from the point of view of evolution is a primitive sign. In most cases, the flowers are collected in groups of 3-4 to several thousand in each, i.e. form inflorescences. Inflorescences are formed in accordance with a certain pattern, specific to the taxon. Probably, the world's first inflorescence was an apical flower, below which two lateral branches grew on short lateral branches: this is characteristic of many modern species, in particular roses. On the lateral branches under the flowers, shoots of the second order can develop, also with flowers at the ends, etc., until a dense inflorescence is formed, called cymose, vermicelli or closed. It is often found in representatives of the clove family, in succulent sedum (Sedum) and bryophyllum (Bryophyllum), etc.
Types of inflorescences. Usually, in a cymosis inflorescence, the order of blooming of flowers corresponds to the order of the branch, at the end of which there is a flower. Another type of inflorescence is called botric, lateral or open: the main axis of the stem continues to grow, successively releasing short lateral shoots with flowers or small inflorescences at the ends from the axils of the apical leaves. At the same time, the apical leaves themselves decrease in the course of evolution, become scaly or disappear altogether, and the central axis is shortened, so that the inflorescence as a whole becomes denser. Blossoming of flowers in it goes, naturally, from the base to the top. The cymose and botric patterns explain all the variety of known inflorescences. For example, the so-called. a simple umbrella in primroses is formed when the central axis stops growing, and the places where the lateral branches leave it approach each other (all branches depart from almost one point) and are surrounded by modified leaves. The marginal flowers correspond to the lower ones and are the first to bloom, so the flowering spreads centripetally - from the periphery to the center. If the lateral branches befell the fate of the central one, a complex umbrella arises, like in carrots and parsley. The flowering of umbellate inflorescences (apicals) of onion, pelargonium or vatnik is, on the contrary, centrifugal, because they are cymoseous in origin. Shortening of the stems of individual flowers can lead to the appearance of capitate inflorescences, such as in clover. Many elongated inflorescences, sometimes complex and unevenly arranged, but similar in that the flowers in them practically "sit" on the central axis, are called ears. The earrings of willows, poplars and oaks are soft hanging ears. Sometimes only a detailed study makes it possible to determine the nature of the inflorescence - it is cymotic, botric or heterogeneous. So, the inflorescences-shields of the viburnum (Viburnum), dogwood and hawthorn are cymotic, flattened on top, and in the cylindrical panicles of lilac, both cymose and botric parts can be found.


TYPES OF FLOWERS.
Sunflower: the inflorescence of the basket consists of two types of flowers - marginal ligulate and tubular forming a central disc. Geranium: dicotyledonous with a five-membered flower.



TYPES OF FLOWERS.
Saffron (crocus) is a monocotyledonous species with a three-membered flower (the number of its different parts is a multiple of three). Sweet pea is a dicotyledonous species with a bilaterally symmetrical flower.


CLASSIFICATION AND EVOLUTION


Monocotyledonous and dicotyledonous. The department of flowering plants is divided into two classes - monocotyledons (Monocotyledonae) and dicotyledons (Dicotyledonae). As the names suggest, they differ in the number of embryo cotyledons. In addition, in monocots, flowers are usually three-membered (i.e., the number of their different parts is a multiple of three), leaf venation, as a rule, is parallel (in essence, their leaves are mainly overgrown leaf petioles without plates), conducting bundles are scattered in the thickness of the stem and do not form a pronounced cylinder, and in the overwhelming majority of cases there is no cambium, therefore, secondary growth in thickness does not occur. In dicotyledons, flowers are usually four- or five-membered, leaf venation is usually reticulate, vascular tissues form a cylinder in the stem, and due to the activity of the cambium, the stem can grow in thickness. Monocots include such well-known large families as cereals, palms, lily and orchids, but dicotyledons are much more numerous and varied.
Flower signs. Angiosperms are divided into families, focusing primarily on the signs of their flowers. The most primitive are considered to be close in structure to magnolia flowers: there are indefinitely many stamens and pistils located spirally on an elongated axis (receptacle), individual parts do not grow together with each other, in general, radial symmetry is preserved. In the flowers of most modern species the number of elements of each type is strictly defined, and they are located in circles, and not in a spiral. So, in the pink family, a primitive trait is preserved - a lot of stamens and pistils, however, the receptacle is no longer axial, but has grown together with their bases into a wide disc or cup-shaped structure with stamens along the edge and pistils in the center. In this family, there are many species with edible fruits, which include a growing fleshy receptacle (strawberries, rose hips). In representatives of the closely related apple family (it is often considered a subfamily of pink ones), the ovaries grow together with each other and with the receptacle surrounding them on all sides, forming a complex structure that becomes a very characteristic fruit when ripe. In legumes, there is only one carpel and, accordingly, a pistil, and there are usually ten stamens, often completely or partially accrete bases in the surrounding tube; the petals are different in shape, and the two lower ones have grown together in a "boat", so that the flower is bilaterally symmetrical. In geraniums, the symmetry of the flower is radial; five-membered flower; sepals, petals and stamens are free, and carpels have grown together in a single column; the receptacle is almost invisible. Many more families can be enumerated, combining primitive and progressive characters in various ways, but there is only one conclusion: the evolution of flowering ones proceeded in different and not always direct paths. The family ties of the families of this department form a complex branching genealogical tree.
Types of ovaries. Many flowering ovaries are the same as those of apple trees, the so-called. lower, i.e. immersed in the receptacle and fused with it. This trait is often combined with a small number of flower parts, its bilateral symmetry, and other progressive traits. In the umbellate family, for example, the ovary is inferior, and the non-accrete stamens, petals and sepals are five, although they are arranged radially symmetrically. In honeysuckle, the ovary is lower, the stamens, petals and sepals are usually five, but the petals are fused with each other and the corolla, to which the stamens are attached, is usually bilaterally symmetrical. In labiates, the petals have grown into a two-lipped corolla, stamens have grown to it (there are two or four of them), but the ovary, in the formation of which two carpels are involved, remains upper, i.e. not immersed in the receptacle. The legume pistil is formed by a single carpel, and the ovary or fruit (pod), when opened, is also leaf-shaped with one row of ovules (seeds) along each edge. If the pistils are formed by several accrete carpels, then in their ovaries on the cut you can often see (for example, in saxifrage and nightshade) the corresponding number of cavities (nests) with ovules inside. In other cases, although the ovary is complex in origin, the partitions between the carpels inside it disappear, and it becomes unilocular, like in violets and primroses. Its nature can be determined by other anatomical details, for example, by the location of the ovules or by the presence of several stigmas in the pistil. So, in violet ovules, they form three vertical rows on the inner wall of the ovary, while in primroses they are attached to the central column extending from its bottom.
Reducing the size of flowers. The most primitive angiosperms have rather large flowers. In the course of evolution, their size, as a rule, decreases, the number of parts decreases, but the relationships become more complex. In many evolutionary lines, some parts of the flower tend to disappear completely. For example, oak, brown, poplar, ash and some other trees often lack sepals and petals, and flowers become dioecious, i.e. in some, only stamens remain, in others - only pistils. In evolutionary terms, such simplification and refinement does not mean degeneration at all, but, on the contrary, a step forward towards a more economical and efficient use of resources. For example, the most successful families are cereals and sedges with their tiny, often dioecious, flowers with little or no perianth.
Complex inflorescences. In parallel with the reduction in size and simplification of flowers, there is a tendency to combine them into large complex inflorescences. They are typical, for example, of cereals and sedges (ears, panicles), umbellates (complex umbrellas), cornelian cherries and honeysuckle (scutes). Compositae (sunflower, chamomile, aster, dandelion, cornflower, etc.) reached a kind of tops in this: their very inflorescence (it is called a basket) is easy to confuse with one large flower... However, it is possible to single out the real miniature flowers that make up it. In a dandelion, for example, they are all the same and consist of a columnar receptacle with an ovary of complex origin immersed in it, but containing only one ovule, sepals modified into thin hairs (crest), petals and stamens. There are five petals: at their bases they have grown together into a short tube, which is stretched from one edge into a long flat ribbon yellow color(many consider it to be one petal). There are also five stamens: their anthers have grown together into the cylinder surrounding the pistil, and the bases have grown to the rim. Thus, the small size does not at all mean the simplicity of the structure and, moreover, the loss of any advantages. In other Compositae, the structure of the basket is even more complicated: the flowers in it are different - in the center are tightly packed tiny tubular (bisexual), and along the edge are larger, ligulate, often differing in color and similar to the "petals" of a dandelion. The marginal flowers can be unisexual (pistillate) or sterile (like a sunflower), i.e. do not form seeds, but attract pollinators with their bright appearance. Some cultivars of dahlia have three types of flowers in the inflorescence.
General evolutionary trend. This trend towards miniaturization of flowers, combining many of them into large inflorescences and differentiation within them into fertile and sterile, attracting pollinators, can be traced in other families. For example, some types of hydrangea (Hydrangea) form voluminous spherical inflorescences with barren, bright flowers around the periphery and barely noticeable fertile inside. The same picture can be seen in the viburnum (Viburnum) - plants from a completely different family. Moreover, there is reason to believe that the angiosperm flower itself originated from a kind of "inflorescence" - a bunch of reproductive shoots, which in the course of evolution increasingly converged, simultaneously acquiring different functions and, accordingly, a different structure. If this hypothesis is correct, then the general line of development of flowering plants can be considered a decrease in size, a thickening of the structure and differentiation of parts serving for reproduction. This trend can be traced in various families with their various combinations of primitive and progressive characters; in favor of the same is evidenced by the parallel tendency towards a reduction and simplification of the whole plant, i.e. to the appearance of herbaceous species, while the first angiosperms were almost certainly trees or shrubs.
Family of flowering plants. The following list of a small number of angiosperm families with some of their well-known representatives is intended only to demonstrate the diversity of these plants and their importance in human life.
Buttercup (Ranunculaceae): buttercups, anemones (anemones), clematis, delphinium, catchment. Cruciferous (Cruciferae): cabbage, turnip, mustard, radish, horseradish. Pink (Rosaceae): roses (rosehip), plum, cherry, almond, peach, raspberry, blackberry, strawberry. Legumes (Leguminosae): Peas, beans, soybeans, alfalfa, clover. Cactaceae (Cactaceae): various cacti. Euphorbiaceae (Euphorbiaceae): many succulents, resembling cacti, but very different from them in the structure of the flower; the rubber tree hevea and the castor oil-producing castor oil plant. Umbelliferae (Umbelliferae): celery, parsley, parsnips, dill, carrots and a number of poisonous plants, such as hemlock (Conium), the infusion of which in ancient times poisoned those sentenced to death. Heather (Ericaceae): heather, blueberry, cranberry, rhododendron, azalea. Solanaceae (Solanaceae): petunia, potatoes, tomatoes, eggplant, paprika and many plants containing biologically active substances, such as tobacco (Nicotiana), belladonna (Atropa), dope (Datura). Pumpkin (Cucurbitaceae): pumpkins, cucumbers, watermelon, melon. Compositae: sunflower, asters, chamomile, dahlias, lettuce, Jerusalem artichoke (earthen pear) and many weeds, such as thistle, thistle, dandelion, ragweed, cocklebur, burdock. All of the families listed above belong to the dicotyledonous class. Of the monocots, we will restrict ourselves to the most famous. Palm trees (Palmae): coconut, date. Cereals (Gramineae): all cereals, in particular wheat, oats, barley, rice, corn; bamboo. Aronicae (Araceae): calla, monstera, philodendron. Liliaceae (Liliaceae): lily, hyacinth, tulip, onion. Amaryllidaceae: daffodil, amaryllis. Iridaceae: iris (iris), freesia, gladiolus (skewer). Orchids (Orchidaceae): various decorative orchids, in particular the lady's slipper; vanilla (Vanilla). see also