Names of brown algae pigments. Brown and Red algae

What is the phenomenon of spirulina? Hundreds of scientists from all over the world have conducted a thorough study of its chemical composition and biological effects on the body of animals and humans. The results of these studies can be found thanks to the works of Hiroshi Nakamuro (Japan), Christopher Hills and Robert Henrichson (USA).

The peculiarity of spirulina is that it is based on photosynthesis - the process of direct absorption of energy from sunlight, which is typical for plant life forms. At the same time, the biochemical composition of the spirulina cell is to some extent similar to the composition of animal cells. The combination of properties of both plant and animal organisms in microalgae cells is another factor determining the high biological value of spirulina.

Spirulina biomass contains absolutely all the substances that a person needs for normal life. A number of special substances - bioprotectors, biocorrectors and biostimulants - are not found in any other product of natural origin. This determines the truly phenomenal properties of spirulina as a food product and a broad-spectrum therapeutic agent.

Blue-green algae, to which spirulina belongs, have a cell wall consisting of murein mucopolymer, which is easily digested by human digestive juices, in contrast, for example, to the single-celled green algae chlorella, which has a cellulose shell, which can only be destroyed by the microflora of ruminants.

Its soft cell wall makes it the most digestible food in the world. Research has shown that spirulina has no equal due to the highest quality protein of plant origin, the highest digestibility of dietary elements, and the saturation of the most essential vitamins and minerals.

The protein content of spirulina (60–70%) is much higher than any other traditional food product. For comparison: eggs contain 47% protein, beef - 18-21%, soybean powder - 37%. In addition, spirulina protein contains all the amino acids necessary (irreplaceable) for the normal functioning of the human body, ensuring the normal development of growing cells and the vital needs of already formed and aging cells.

Spirulina contains 10 to 20% sugars, which are easily digested with a minimal amount of insulin. Spirulina contains very little cholesterol (32.5 mg/100 g), while an egg contains 300 mg for the same amount of protein, so regular consumption of spirulina leads to a decrease in cholesterol in the body. Its composition includes up to 8% fat, represented by the most important fatty acids (lauric, palmitic, stearic, oleic, linoleic, β-linolenic, β-linolenic, etc.). In particular, ?-linolenic acid is of great value in the treatment of impotence in men, frigidity, lack of libido in women, etc. In combination with vitamin E, these components improve the function of reproductive organs, promote the onset and normal course of pregnancy, and after childbirth increase milk production Spirulina is enriched with macro- and microelements necessary for the normal course of metabolic processes in the body. And, what is especially important, spirulina contains the most important vitamins - A, B, B, B, B - in optimal proportions. 6 , IN 12 , PP, biotin, folic acid, pantothenate, C and E.

Spirulina is the richest in beta-carotene content, it contains 10 times more than carrots. Beta-carotene is one of the most powerful antioxidants and immunostimulants that prevent the development of cardiovascular diseases and cancer. Under optimal cultivation conditions, spirulina accumulates beta-carotene in an amount of 3000 mcg/g or more, which is many times higher than its concentration in traditional products. A normal level of beta-carotene in human blood plasma (0.5–1.5 µmol/l) can be achieved by daily additional (in addition to food) intake of 2–6 mg of the vitamin per day. This amount of beta-carotene is contained in only 1-2 g of spirulina. Wherein The therapeutic and prophylactic effect of spirulina beta-carotene is several times greater than that of synthetic beta-carotene currently used in medicine.

Spirulina contains much more B vitamins than meat products, legumes and various cereals, during culinary processing of which up to 40% of the latter is destroyed. 1 g of dry mass of spirulina contains: thiamine (B 1 ) – 30–50 mcg, riboflavin (B 2 ) – 5.5–35 mcg, pyridoxine (B 6 ) – 3–8 mcg, cyanocobolamin (B 12 ) – 1–3 mcg. Spirulina is especially rich in vitamin B 12 (taking into account digestibility, 1 g of spirulina is equal to 100 g of boiled meat). It is high in vitamin B 12 explains the high positive therapeutic effect noted when taking spirulina in patients with hematopoietic disorders (primarily anemia of various natures), lipid metabolism (hypercholesterolemia), fatty liver degeneration, polyneuritis and neuralgia. Spirulina also contains folic acid (vitamin B 9 ) (0.1–0.5 mcg/g), niacin (vitamin B 3 ) (118 mcg/g), inositol (vitamin B) (350–640 mcg/g), biotin (vitamin H) (0.012–0.05 mcg/g), ascorbic acid (vitamin C) (2120 mcg/g) , β-tocopherol (vitamin E) (190 μg/g). In terms of vitamin PP content, spirulina is much superior to beef liver, kidneys, tongue, poultry and rabbit meat.

The usefulness of spirulina vitamins lies in their balanced complex. According to modern ideas, natural balanced complexes of antioxidants (beta-carotene, alpha-tocopherol, folic acid, iron, selenium, etc.) contained in plant foods, such as spirulina. despite the low concentrations (not comparable to the currently recommended daily requirements), they have a more pronounced protective effect on the human body than large doses of individual synthetic vitamins or their mixtures, which do not always provide a noticeable positive effect and sometimes cause harm. This, according to many researchers, largely determines the repeatedly confirmed immunostimulating, radioprotective and antitumor properties of spirulina.

Spirulina contains almost the entire set of minerals a person needs. Moreover, they are found in spirulina in an easily digestible form. The content of phosphorus, calcium and magnesium in spirulina is significantly higher (about 2-3 times) than in plant and animal products rich in these elements (peas, peanuts, raisins, apples, oranges, carrots, fish, beef, etc.) But The most important thing is that the minerals contained in plant foods and cooked processed meats (fish) are less absorbed than those contained in spirulina. Iron, vital for the human hematopoietic system (part of hemoglobin, red blood cells, muscle myoglobin and enzymes), is absorbed by the body 60% better than other supplements such as ferrous sulfate. Taking 4 g of spirulina per day provides a rapid increase in hemoglobin in the blood. The increased content of microelements such as zinc, selenium, chromium, iodine, iron, copper, and manganese in spirulina deserves special attention.

Spirulina contains three dye pigments: carotenoids, chlorophyll and phycocyanin, which help the body synthesize many enzymes necessary to regulate the body's metabolism. The most important of these for humans is the blue pigment phycocyanin. Research conducted by Japanese and American doctors shows that phycocyanin strengthens the immune system and increases the activity of the body's lymphatic system. Its main function is protective, aimed at maintaining healthy organs and tissues of the body and protecting against infections and other diseases.

Spirulina chlorophyll has a structure and chemical composition close to the heme molecule in the blood. In combination with the complex of substances contained in spirulina, it promotes the biosynthesis of hemoglobin, which allows you to normalize the function of the hematopoietic organs in a short time.

Thus, spirulina, which contains complete protein, carbohydrates, fats, micro- and macroelements, vitamins, phycocyanin, beta-carotene, β-linoleic acid and other biologically active components, is capable of each individually, and especially together, providing a powerful a positive effect on the human body and contribute to the normalization of existing disorders, if necessary, or increase the body’s defenses and, as a consequence, its performance and resistance to adverse environmental factors.

Kelp

Brown algae are an excellent raw material for the production of a number of medicines and biologically active food additives.

A feature of the composition of brown algae, which includes kelp, is the high content of alginic acid and its salts (13–54% of dry residue), which are absent in green and red algae. In addition to alginic acid, kelp also contains other polysaccharides: fucoidan and laminarin.

A sensational discovery made in Japan is associated with fucoidan. Scientists have noticed that the island of Okinawa has the lowest level of cancer. Numerous studies have been conducted. It turned out that the inhabitants of the island of Okinawa eat brown seaweed raw, while the rest of the Japanese eat it boiled. It turned out that the reason is the polysaccharides fucoidan and laminarin. When they enter the human body, cancer cells begin to die. But fucoidan breaks down when boiled. Fucoidan prevents the process of cell adhesion and prevents metastasis. By stimulating phagocytosis, alginates, fucoidan and laminarin have an antitumor effect, destroying not only cancer cells, but also metastases in the later stages of cancer. Fucoidan and laminarin are effective not only against a wide variety of forms of cancer, but also help restore the body functions of patients who have undergone intensive chemotherapy and radiation therapy. The recovery process is much faster, the general condition of the body improves, lost hair grows back, and liver function is restored.

Another property of fucoidan and laminarin polysaccharides is the prevention and treatment of cardiovascular diseases. These diseases largely depend on the balance of lipids, the imbalance of which leads to an increased tendency to form atherosclerotic plaques in blood vessels. Polysaccharides fucoidan and laminarin help correct the situation, especially when the disease has not yet developed. Laminarin also has a hypotensive effect and exhibits anticoagulant activity, which is 30% of the activity of heparin, prevents the manifestations of radiation sickness, and protects against the destructive effects of ionizing radiation.

It is now known that fucoidan is a regulator of metabolic processes and an immunocorrector, the action of which is based on the activation of natural defense mechanisms against pathogenic microorganisms. Polysaccharides fucoidan and laminarin stimulate phagocytosis. Phagocyte cells are the main orderlies in the body; they capture and digest microorganisms and their decay products.

But still, the main active ingredient of kelp is alginic acid. Alginic acid was first discovered in 1883 by Stanford. The applied significance of alginic acid and its derivatives is determined by its structure, formed in the process of natural biosynthesis in brown algae of various regions of the world ocean. Currently, a number of researchers claim that it is a high molecular weight polysaccharide consisting of D-mannuronic and L-hyaluronic acids. Their ratio in alginates mined in different countries is noticeably different, which in turn determines the difference in physicochemical properties. It is the complex of these properties of alginates, in particular the ability to form viscous aqueous solutions, even pastes, homogenizing and emulsion properties, film-forming ability and a number of others, that served as the basis for the widespread use of these substances in various industries, including pharmaceuticals.

In modern medicine, there are three main areas of use of alginates:

1) as auxiliary chemical and pharmaceutical substances for the production of various dosage forms of medicines;

2) as medical products in the form of gauze, cotton wool, napkins, sponges and others for local hemostasis during external and intracavitary bleeding;

3) as medicines and dietary supplements of various directions of action.

The widespread use of alginates is due to their practical harmlessness and good tolerability.

Alginic acid and its salts have a number of useful properties, but at the same time they are distinguished by unique qualities inherent only to them. Externally, alginates are a jelly-like substance, the adhesive strength of which is 14 times greater than that of starch, and that of gum arabic by 37 times. This property has made it possible to use them in various industries as thickeners and gelling agents.

Alginic acid and its salts have a number of unique healing properties, some of which are due to their jelly-like consistency. The property of alginic acid and its salts to stop bleeding has proven useful in the treatment of ulcerative lesions of the gastrointestinal tract.

Alginic acid salts, when taken orally, have antacid properties (reduce aggressive hyperacidity of gastric juice) and stimulate the healing of ulcerative lesions of the gastric and intestinal mucosa. Once in the gastrointestinal tract, alginates interact with hydrochloric acid of gastric juice and form a gel that covers the mucous membrane, protecting it from further exposure to hydrochloric acid and pepsin, stopping bleeding.

The positive effect on the gastrointestinal tract and digestive processes is also associated with the ability of alginates to have a pronounced sorbing effect. They are able to bind and remove breakdown products of carbohydrates, fats and proteins, heavy metal salts and radionuclides from the body. This also made it possible to use alginates in the complex treatment of dysbiosis, neutralizing by-products that interfere with the development of normal natural intestinal flora. Research has found that alginates retain their own intestinal microflora, suppressing the activity of pathogenic bacteria such as staphylococcus, Candida fungi, etc. Alginates exhibit an antimicrobial effect even in small concentrations.

Alginates are able to enhance weakened peristalsis of the intestine and gallbladder ducts, which allows their use in cases of weakened intestinal motor activity (flatulence and bloating), as well as in case of biliary dyskinesia.

Alginates are widely used to maintain and restore a damaged immune system, as they have unique immunostimulating abilities. First of all, alginates stimulate phagocytosis. Stimulation of phagocytic defense provides antimicrobial, antifungal and antiviral activity of kelp preparations. Alginates are capable of sorbing (binding) excess amounts of a special class of immunoglobulins (E), which are involved in the development of acute allergic diseases and reactions. The hypoallergenic effect is especially inherent in calcium alginate, which, due to the content of calcium ions, prevents the release of biologically active substances (histamine, serotonin, bradykinin, etc.), as a result of which allergic inflammation does not develop.

Alginates stimulate the synthesis of local specific defense antibodies (class A immunoglobulins). This in turn makes the skin and mucous membranes of the respiratory tract and gastrointestinal tract more resistant to the pathogenic effects of microbes.

Alginates are also used topically for the treatment of periodontitis, cervical erosions, gastric and duodenal ulcers.

Surgeons widely use self-absorbable wound-healing dressings made on the basis of alginates to treat wounds, burns, trophic ulcers, and bedsores. Alginate dressings have good drainage properties, absorb wound exudate, promoting rapid wound cleansing, and reduce intoxication of the body. The dressings have hemostatic properties and stimulate tissue regeneration processes.

The anti-sclerotic effect of kelp is explained by the presence in its composition of a cholesterol antagonist - betasitosterol. It helps dissolve cholesterol deposits deposited on the walls of blood vessels. In addition, the biologically active components of algae activate human enzyme systems, which also helps cleanse blood vessels. The decrease in cholesterol levels in the blood is largely due to the presence of polyunsaturated fatty acids in kelp. Hormone-like substances with anti-sclerotic effects have been found in algae. The laxative effect is associated with the ability of kelp powder to swell greatly and, increasing in volume, irritate the receptors of the intestinal mucosa, which enhances peristalsis. The enveloping effect of alginic acid helps to delay the absorption of water in the intestine, which leads to normalization of stool. The favorable combination of fiber and mineral salts in seaweed not only eliminates constipation, but also regulates the impaired function of the digestive organs for a long time.

Food products from kelp are significantly inferior in content and qualitative composition of proteins and carbohydrates to food products prepared from terrestrial plants, but they have valuable properties that plant food raw materials of terrestrial origin do not possess. These properties include the following:

1) the ability to absorb large amounts of water and increase in volume;

3) higher content of various macro- and microelements than in terrestrial plants.

In this regard, seaweed in the diet should be considered not as a source to cover the body’s energy costs, but as a dietary ingredient.

Algae, to a greater extent than other living creatures of the underwater kingdom, have the ability to extract and accumulate numerous elements from sea water. Thus, the concentration of magnesium in seaweed exceeds that in sea water by 9–10 times, sulfur by 17 times, and bromine by 13 times. 1 kg of kelp contains as much iodine as it is dissolved in 100,000 liters of sea water.

In terms of the content of many chemical elements, algae are significantly superior to terrestrial plants. Thus, boron in algae is 90 times more than in oats, 4–5 times more than in potatoes and beets. The amount of iodine in kelp is several thousand times greater than in terrestrial flora. The mineral substances of algae are mainly (75–85%) represented by water-soluble potassium and sodium salts (chlorides, sulfates). Seaweed contains a fairly large amount of calcium: 100 g of seaweed contains 155 mg. Dry seaweed contains an average of 0.43% phosphorus, while dried potatoes and dried carrots contain almost half as much.

Algae accumulate in large quantities not only various micro- and macroelements, but also many vitamins. Kelp contains an amount of provitamin A that corresponds to its content in common fruits: apples, plums, cherries, oranges. By vitamin B content 1 kelp is not inferior to dry yeast. 100 g of dry brown algae contains up to 10 mcg of vitamin B 12 . Algae are of great interest as a source of vitamin C in the diet. Kelp contains a fairly large amount of this vitamin: 100 g of dry kelp contains from 15 to 240 mg, and raw algae contains 30–47 mg. In terms of the content of this vitamin, brown algae is not inferior to oranges, pineapples, strawberries, gooseberries, green onions, and sorrel. In addition to the above vitamins, other vitamins were found in algae, in particular vitamins D, K, PP (nicotinic acid), pantothenic and folic acids.

Sea plants contain enormous amounts of iodine. Thus, in 100 g of dry kelp, the iodine content ranges from 160 to 800 mg. It is known that in brown edible algae up to 95% of iodine is in the form of organic compounds, of which approximately 10% is associated with protein, which is of no small importance. In addition, sea kale contains a certain amount of mono- and diiodotyrosine - inactive hormonal substances contained in the thyroid tissue, which are also organic products.

Thus, an artificially created product cannot compete with living nature: sea kale does not just have a lot of iodine - it also contains biologically active substances that help absorb this iodine. Organic iodine compounds in kelp help normalize thyroid function faster than an equivalent amount of sodium iodide. And this can be explained not only by iodine, but also by the content of macro- and microelements (molybdenum, copper, cobalt, etc.) and vitamins in marine plants that are important for metabolic processes.

Red seaweed

Widespread in the Far Eastern seas, red algae, used for a long time in food and medical practice, contain various hydrocolloids, including carrageenan. Carrageenans, sulfated polysaccharides, are found only in red seaweed, have no analogues among other plant polysaccharides and are widely used in both the pharmaceutical and food industries. Industrial interest in carrageenans is due to their ability to form gels, increase the viscosity of aqueous solutions, as well as their versatile biological activity.

There are several types of carrageenans, which can be divided into so-called gelling and non-gelling ones. Each plant species may contain several types of carrageenans. In addition, the composition and amount of extracted carrageenan depend on the location of the algae, the phase of its life cycle and the season. The practical use of carrageenan is largely determined by its physicochemical properties. Structural differences in carrageenans significantly affect their biological activity. Carrageenans exhibit high anticoagulant activity at low concentrations. They are used as an enterosorbent and radioprotector. There are positive results when using carrageenans in patients with atherosclerosis and duodenal ulcers.

The beneficial properties of carrageenans open up a unique opportunity to create therapeutic and prophylactic products based on them. For the needs of production, a recipe for various confectionery jellies has been developed based on carrageenan, which can be used for dietary nutrition.

All algae differ well in their set of photosynthetic pigments. Such groups in plant taxonomy have the status of divisions.

The main pigment of all algae is the green pigment chlorophyll. There are four known types of chlorophyll, which differ in their structure: chlorophyll a– present in all algae and higher plants; chlorophyll b– found in green, charophyte, euglenoid algae and higher plants: plants containing this chlorophyll always have a bright green color; chlorophyll c– found in heterokont algae; chlorophyll d– a rare form, found in red and blue-green algae. Most photosynthetic plants contain two different chlorophylls, one of which is always chlorophyll a. In some cases, instead of the second chlorophyll, there are biliproteins. There are two types of biliproteins found in blue-green and red algae: phycocyanin– blue pigment, phycoerythrin- red pigment.

The obligatory pigments included in photosynthetic membranes are yellow pigments - carotenoids. They differ from chlorophylls in the spectrum of absorbed light and are believed to perform a protective function, protecting chlorophyll molecules from the destructive effects of molecular oxygen.

In addition to the listed pigments, algae also contain: fucoxanthin– golden pigment; xanthophyll- brown pigment.

End of work -

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Seaweed

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Cell covers
Cell covers ensure the resistance of the internal contents of cells to external influences and give the cells a certain shape. The covers are permeable to water and low molecules dissolved in it

Flagella
Monadic vegetative cells and monadic stages in the life cycle (zoospores and gametes) of algae are equipped with flagella - long and rather thick cell outgrowths, externally covered with plasmalemma. AND

Mitochondria
Mitochondria are found in eukaryotic algae cells. The shape and structure of mitochondria in algae cells are more diverse compared to mitochondria of higher plants. They may be round

Plastids
Pigments in the cells of eukaryotic algae are located in plastids, as in all plants. There are two types of plastids in algae: colored chloroplasts (chromatophores) and colorless leucoplasts (ami

Nucleus and mitotic apparatus
The algae nucleus has a structure typical of eukaryotes. The number of nuclei in a cell can vary from one to several. On the outside, the core is covered with a shell consisting of two membranes, the outer membrane

Monadic (flagellar) type of thallus structure
The most characteristic feature defining this type of structure is the presence of flagella, with the help of which monadic organisms actively move in the aquatic environment (Fig. 9, A). Movable w

Rhizopodial (amoeboid) type of structure
The most significant features of the amoeboid type of structure are the absence of strong cell covers and the ability for amoeboid movement, with the help of qi temporarily formed on the surface of the cell

Palmelloid (hemimonadal) type of structure
Characteristic of this type of structure is the combination of a stationary plant lifestyle with the presence of cellular organelles characteristic of monadic organisms: contractile vacuoles, stigma, tourniquet

Coccoid type of structure
This type combines unicellular and colonial algae, immobile in a vegetative state. Cells of the coccoid type are covered with a membrane and have a plant-type protoplast (tonoplast without socrates

Trichal (filamentous) type of structure
A characteristic feature of the filamentous type of structure is the filamentous arrangement of immobile cells, which are formed vegetatively as a result of cell division, which occurs predominantly

Heterotrichal (non-filamentous) type of structure
The heterofilamentous type arose on the basis of the filamentous type. The heterofilamentous thallus consists mostly of horizontal threads creeping along the substrate, performing the function of attachment, and vertical ones, along

Parenchymal (tissue) type of structure
One of the directions in the evolution of the heterofilamentous thallus was associated with the emergence of parenchymatous thalli. The ability for unlimited growth and division of cells in different directions led to the evolution

Siphonal type of structure
The siphonal (non-cellular) type of structure is characterized by the absence of cells inside the thallus, which reaches relatively large, usually macroscopic sizes and a certain degree of differentiation

Siphonocladal type of structure
The main feature of the siphonocladal type of structure is the ability to form complexly arranged thalluses, consisting of primarily multinucleated segments, from the primary noncellular thallus. IN

Asexual reproduction
Asexual reproduction of algae is carried out with the help of specialized cells - spores. Sporulation is usually accompanied by division of the protoplast into parts and the release of fission products from

Simple division
This method of reproduction is found only in unicellular forms of algae. Division occurs most simply in cells that have an amoeboid type of body structure. Division of amoeboid forms

Fragmentation
Fragmentation is inherent in all groups of multicellular algae and manifests itself in different forms: the formation of hormogoniums, regeneration of detached parts of the thallus, spontaneous loss of branches, regrowth

Reproduction by shoots, stolons, brood buds, nodules, akinetes
In the tissue forms of green, brown and red algae, vegetative reproduction takes on its complete form, which differs little from the vegetative reproduction of higher plants. Keeping the way

Sexual reproduction
Sexual reproduction in algae is associated with the sexual process, which consists of the fusion of two cells, resulting in the formation of a zygote that grows into a new individual or produces zoospores.

Change of nuclear phases
During the sexual process, as a result of the fusion of gametes and their nuclei, the number of chromosomes in the nucleus doubles. At a certain stage of the development cycle, during meiosis, a reduction in the number of chromosomes occurs, as a result

Endophytes/endozoites, or endosymbionts
Endosymbionts, or intracellular symbionts, are algae that live in the tissues or cells of other organisms (invertebrate animals or algae). They form a kind of ecological group

Department of blue-green algae (cyanobacteria) - cyanophyta
The name of the department (from the Greek cyanos - blue) reflects a characteristic feature of these algae - the color of the thallus, associated with a relatively high content of the blue pigment phycocyanin. Cyanogen

Order – Chroococcales
They occur as single-celled “simple” individuals or more often form mucous colonies. When cells divide in two planes, single-layer lamellar colonies appear. Division in three points

Department of red algae – rhodophyta
The name of the department comes from the Greek word rhodon ("rodon") - pink. The color of red algae is due to different combinations of pigments. It comes in gray and purple

Order Banguiaceae–Bangiales
The genus Porphyra has a thallus in the form of a thin shiny plate with smooth or folded edges, consisting of one or two layers of tightly connected cells. The base of the plate usually goes into

Order Rhodymeniales
Genus Sparlingia (Rodimenia) - flat plates up to 45 cm in height, leaf-shaped and wedge-shaped, widened and palmately dissected at the top, from light pink or light orange to

Order Coralline - Corallinales
The genus Coralline is a segmented, fan-shaped, branched bush up to 10 cm in height, branched, calcareous, from pink-lilac to almost white. Reproduces asexually and sexually. Spo

Order Gigartinales – Gigartinales
Genus Hondrus - dense leathery cartilaginous bushes up to 20 cm in height, 3-4 times branched, light yellow, light pink, purple-dark red. Grows in the lower part of the littoral zone and

Order Ceramiaceae – Ceramiales
The genus Ceramium is a delicate, fluffy, segmented bush up to 10 cm in height, dichotomously or alternately branched, dark yellow with a pinkish tint. Branching of two to four orders, of course

Division of diatoms - bacillariophyta
The department is called Diatoms (from the Greek di - two, tome - cut, dissection), or Bacillaria (bacillum - stick). Includes unicellular solitary or colonial org.

Division of heterokont algae (heterokontophyta)
All heterokonts have a similar structure of the flagellar apparatus. There are 2 flagella, and one of them has very characteristic tubular three-membered feathery outgrowths, or hairs - mastigonemes. Exactly cash

Taxonomy
Fossil coccoliths are known from Mesozoic deposits and were abundant throughout most of the Jurassic and Cretaceous periods. Prymnesiophytes reached their maximum diversity in the Late Cretaceous,

Department of cryptophyte algae (cryptomonads) – cryptophyta
The department is named after the type genus Cryptomonas (from the Greek kryptos - hidden, monas - individual). Includes single-celled, motile, monadic organisms. Cryptophyte cells

A B C D E
Rice. 53. Appearance of cryptophyte algae (according to: G.A. Belyakova et al., 2006): A – Rodomonas, B – Chroomonas, C – Cryptomonas, D – Chilomonas, E – Goniomonas can for

Department of green algae – chlorophyta
Green algae are the most extensive of all algae divisions, numbering, according to various estimates, from 4 to 13 - 20 thousand species. All of them have a green color of the thalli, which is due to the predominance of chlorine

Order Ulothrixales – Ulotrichales
Genus Ulothrix (Fig. 54). Species of Ulotrix live more often in fresh water, less often in sea, brackish water bodies and in soil. They attach to underwater objects, forming bright green bushes.

Order Bryopsidae – Bryopsidales
Most species are found in fresh and brackish waters. Some of them grow on soil, on stones, sand and sometimes on salt marshes. Genus Bryopsis - filamentous bushes up to 6-8 s

Order Volvocales - Volvocales
The genus Chlamydomonas (Fig. 57) includes over 500 species of unicellular algae that live in fresh, small, well-heated and polluted water bodies: ponds, puddles, ditches, etc. Etc

Division Charophyta (Characeae) – Charophyta
Charophytes are a line of freshwater green algae that led to higher plants. These are forms predominantly with filamentous thallus. Often the thallus is vertical, dissected and carries about

Division dinophytes (dinoflagellates) – dinophyta
1. The name of the department comes from the Greek. dineo - to rotate. Unites predominantly unicellular monadic, less often coccoid, amoeboid or palmelloid, sometimes colonial

Division euglenozoa - euglenovae
The department is named after the type genus - Euglena (from the Greek eu - well developed, glene - pupil, eye). Unites single monadic or amoeboid representatives. Occasionally meet

Glossary of terms
Autogamy is sexual reproduction in which two sister haploid nuclei fuse in a common cytoplasm. Autospore is a structure of asexual reproduction, which is

Today, green algae are considered the most extensive group, which has about 20 thousand species. This includes both unicellular organisms and colonial forms, as well as plants with large multicellular thallus. There are representatives that live in water (sea and fresh), as well as organisms adapted to survive on land in conditions of high humidity.

Department Green algae: brief description

The main distinguishing feature of representatives of this group is their coloring - all species are characterized by green or green-yellow coloring. This is due to the main pigment of cells - chlorophyll.

As already mentioned, the department brings together completely different representatives. There are unicellular and colonial forms, as well as multicellular organisms with a large, differentiated thallus. Some unicellular representatives move with the help of flagella; multicellular ones, as a rule, are attached to the bottom or live in the water column.

Although there are organisms with naked cells, most representatives possess a cell wall. The main structural component of the cell membrane is cellulose, which, by the way, is considered an important systematic characteristic.

The number, size and shape of chloroplasts in a cell may vary depending on the type of plant. The main pigment is chlorophyll, in particular the a and b forms. As for carotenoids, plastids contain mainly beta-carotene and lutein, as well as small amounts of neosanthin, zeaxanthin and violaxanthin. Interestingly, the cells of some organisms have an intense yellow or even orange color - this is due to the accumulation of carotenes outside the chloroplast.

Some unicellular green algae have a specific structure - an eye, which reacts to light in the blue and green spectrum.

The main storage product is starch, the granules of which are contained mainly in plastids. Only some representatives of the order have reserve substances deposited in the cytoplasm.

Department Green algae: methods of reproduction

In fact, representatives of this order are characterized by almost all possible methods of reproduction. can occur through (unicellular representatives without a cell membrane), fragmentation of the thallus (this method is typical for multicellular and colonial forms). In some species, specific nodules are formed.

Asexual reproduction is represented by the following forms:

zoospores - cells with flagella, capable of active movement;
aplanospores - such spores do not have a flagellar apparatus, but well-developed cells are not capable of active movement;
autospores - this type of spores is primarily associated with adaptation to the external environment. In this form, the body can wait out dry conditions and other unfavorable conditions.

Sexual reproduction can also be diverse - this includes oogamy, heterogamy, hologamy, as well as isogamy and conjugation.

Order Green algae: characteristics of some representatives

This group includes many famous representatives of the plant world. For example, spirogyra and chlorella are also included in the order.

Chlamydomonas is a fairly well-known genus of green algae, which is of great practical importance. This group includes single-celled organisms with a red eye and a large chromatophore that contains pigments. It is Chlamydomonas that causes the “blooming” of ponds, puddles and aquariums. In the presence of sunlight, organic matter is produced through photosynthesis. But this organism can absorb substances from the external environment. Therefore, chlamydomonas is often used to purify water.

Red - phycoerythrin , orange - carotene And " xanthophyll". Additional pigments affect the color of algae and serve as an important systematic feature. Algae are divided into several types. Typical representatives of microscopic algae are shown in the figure.

Microscopic algae.
A. Diatoms B. Blue-green algae, C. Green algae (Chlamydomonas)

Green algae

Green algae are widespread in surface waters. Among them there are unicellular, multicellular and colonial forms. Pigments are concentrated in special plasma bodies of various shapes - chromatophores. They reproduce by division of the cytoplasm to form daughter cells or sexually. Some species reproduce by producing motile spores. Colonies are formed by asexual division in which daughter cells remain associated with each other. Green algae cells have a variety of shapes: spherical, oval, crescent-shaped, triangular, etc. Their cells contain organelles characteristic of the cells of higher plants. The nucleus is differentiated. The shell consists of cellulose. The cytoplasm may contain grains of starch, which is a product of photosynthesis. The most common unicellular forms of chlorella ( Chlorella vulgaris), Chlamydomonas ( Chlamidomonas), from the colonial ones - Volvox ( Volvox aureus), gonium ( Gonium pectorale), from multicellular - ulothrix. Green algae are found in reservoirs with clean and dirty water, with slow and fast currents, in various pits, puddles that fill after rain, and also on the soil.

Blue-green algae

Blue-green algae ( cyanobacteria ) is considered the oldest of the currently existing plants. These are single- or multicellular organisms, the most simply organized, characterized by a special cell structure. It does not have a typical nucleus and chromatophores. The protoplasm of blue-green algae is differentiated into a peripherally colored layer - chromotoplasm , and the central part – centroplasm . Assimilating photosensitive pigments are chlorophyll, phycocin, phycoerythrin and carotene. Depending on the quantitative ratio of pigments, the color of the cells also changes. The cells contain special bodies - endoplasts dense or viscous consistency. In the plasmatic walls of the cells between the endoplasts there is a “chromatin substance” that stains with nuclear dyes. The cells of blue-green algae lack vacuoles filled with cell sap. In this regard, during plasmolysis, the cell shrinks entirely. The cells of these organisms contain gas vacuoles, which facilitate their floating to the surface. Blue-green algae cells have a membrane. It can be thin and barely noticeable or thickened. Cell membranes are often covered with mucus, which leads to the formation of colonies due to the clumping of this mucus. The composition of the shells consists mainly of pectins. As a rule, colonies do not have a specific shape. In filamentous cells, the rows of cells are enclosed in a hollow cylindrical sheath that covers the entire row of cells. A collection of cells with a sheath is called a filament. Cells within the same filament can be the same or different in size and shape. The cells of the filament are covered with a common mucous sheath on top. In some species, the threads are capable of branching. Formation is often observed heterocyst located in a thread through a certain number of cells. Heterocysts are formed from vegetative cells, but are significantly larger in size. They have a dense shell, but communicate with neighboring cells through pores. It is believed that heterocysts are specialized cells that perform nitrogen fixation.

Many species of cyanobacteria are capable of forming spores. In some species, spores, like true bacteria, are the form that is most resistant to unfavorable conditions. In this case, only one spore is formed from one cell. In other cyanobacteria, spores, like fungi, serve as a method of reproduction. In this case, many small spores are formed inside the mother cell, released when the membrane ruptures. Blue-green algae are very common in nature: they grow in bodies of salt and fresh water, in soils and on rocks, in the Arctic and deserts. This is facilitated by extreme resistance to adverse conditions and undemanding requirements for nutrients.

Diatoms

Diatoms ( Diatomea). They are single-celled microscopic organisms. Some species form colonies in the form of threads, ribbons, and bushes. Cells range in size from 4 to 1500 microns, and colonies sometimes reach several centimeters. Diatom cells contain a formed nucleus and chloroplasts. The latter, in addition to chlorophyll, contain brown pigments, so the color of the algae is yellowish or dark brown. The cells have a pectin shell and a shell consisting of silica. The cell membrane consists of two halves that do not grow together and can move apart. Protoplasm is located in a thin layer along the walls, forming a protoplasmic bridge in the middle of the cell in many species, the rest of the cell space is filled with cell sap, there is only one nucleus. Chromatophores vary in shape. The products of assimilation are oil, volutin, leukosine. They reproduce by simple division and spores. During vegetative division, each part receives a maternal valve, and the missing one grows anew during the development of the cell. The structure of the silicon shell is a distinctive feature of the species. Diatom group Pennales found mainly among fouling of bottom objects and in the soil.

Far Eastern State Technical

fisheries university

Institute of Marine Biology named after. A.V. Zhirmunsky Far Eastern Branch of the Russian Academy of Sciences

L.L. Arbuzova

I.R. Levenets

Seaweed

Reviewers:

– V.G. Chavtur, Doctor of Biological Sciences, Professor of the Department of Marine Biology and Aquaculture of the Far Eastern State University

– S.V. Nesterova, Ph.D., senior researcher at the Laboratory of Flora of the Far East, Botanical Garden-Institute, Far Eastern Branch of the Russian Academy of Sciences

Arbuzova L.L., Levenets I.R. Algae: Study. village Vladivostok: Dalrybvtuz, IBM FEB RAS, 2010. 177 p.

The manual provides modern information about the anatomy, morphology, taxonomy, lifestyle and practical significance of algae.

The textbook is intended for bachelor students in the areas of “Aquatic Bioresources and Aquaculture” and “Ecology and Environmental Management” full-time and part-time, masters of ecology, biology, ichthyology and fish farming.

©Far Eastern State

technical fishery

university, 2010

©Institute of Marine Biology named after. A.V. Zhirmunsky Far Eastern Branch of the Russian Academy of Sciences, 2010

ISBN ……………………..

Introduction…………………………………………………………………………………

1. Structure of algae cells……………………………………

2. General characteristics of algae……………………………

2.1. Types of food………………………………………………………

2.2. Types of thalli…………………………………………………..

2.3. Reproduction of algae……………………………………..

2.4. Life cycles of algae……………………………….

3. Ecological groups of algae…………………………….

3.1. Algae of aquatic habitats…………………………..

3.1.1. Phytoplankton………………………………………………….

3.1.2. Phytobenthos……………………………………………………..

3.1.3. Algae of extreme aquatic ecosystems……………

3.2. Algae of non-aquatic habitats………………………

3.2.1. Aerophilic algae…………………………………….

3.2.2. Edaphilic algae…………………………………….

3.2.3. Lithophilic algae……………………………………..

4. The role of algae in nature and practical significance………

5. Modern taxonomy of algae………………………..

5.1. Prokaryotic algae………………………………..

5.1.1. Department Blue-green algae………………………

5.2. Eukaryotic algae…………………………………….

5.2.1. Department Red algae…………………………….

5.2.2. Division Diatoms………………………..

5.2.3. Department Heterokont algae…………………….

Class Brown algae …………………………………

Class Golden algae …………………………

Class Sinura algae …………………………..

Class Pheotamnia algae………………………

Class Raphid algae ………………………….

Class Eustigma algae …………………………

Class Yellow-green algae………………………

5.2.4. Department Prymnesiophyte algae……………….

5.2.5. Department Cryptophyte algae……………………

5.2.6. Department Green algae…………………….………

5.2.7. Division of Characeae…………………………….

5.2.8. Department Dinophyte algae………………………

5.2.9. Section Euglena algae …………………………

Literature………………………………………………………………………………

Glossary of terms……………………………………………………….

Application …………………………………………………………….

INTRODUCTION

Algae traditionally comprise a diverse group of thallus, photosynthetic, spore-bearing, avascular organisms. Like all lower plants, the reproductive organs of algae are devoid of integument, the body is not divided into organs, and there are no tissues. Among algae there are both eukaryotic and prokaryotic forms. The latter, unlike chlorobacteria, release free oxygen into the environment during photosynthesis.

Algae occupy a dominant position in both fresh and marine waters. Being the main producers, they largely determine the fish productivity of aquatic ecosystems. Thanks to photosynthetic activity, algae enrich the water with oxygen and reduce the amount of carbon dioxide. They have a unique ability to accumulate various harmful substances from the surrounding aquatic environment, as well as release metabolites into the environment that suppress the growth of pathogenic microorganisms. Algae, by changing the chemical composition of water, often contribute to its purification. The qualitative and quantitative composition of algae groups is an important indicator of the ecological state of water bodies. A number of species are used as indicators of aquatic pollution.

The study of algae is an important stage in the training of specialists in the field of mariculture, fish farming and marine ecology. Knowledge of the structure, ecology and systematics of algae is basic for the study of hygrobiology, ichthyology, ecology, ichthyotoxicology; they are also necessary for assessing the raw material base of reservoirs and drawing up fishing forecasts.

Recently, thanks to modern methodological techniques, new information has been obtained about the fine structure, physiology and biochemistry of algae, which has caused a revision of traditional ideas. The taxonomy of lower plants, which include algae, has undergone the greatest changes. At the same time, modern information about the systematics and structure of algae is not reflected in educational literature on botany, and special literature on phycology is not available to a wide student audience.

This textbook provides the latest information about the structure, morphology, taxonomy, ecology and practical significance of algae. A description of the most significant algae taxa is given.

The textbook is intended for bachelor students in the areas of “Aquatic Bioresources and Aquaculture” and “Ecology and Environmental Management” of full-time and part-time forms of study, masters in the field of ecology, ichthyology, fish farming and aquaculture.

Teachers from Dalrybvtuz and specialists in the field of hydrobiology and phycology of the Far Eastern Branch of the Russian Academy of Sciences took part in the preparation of materials for this manual.

1. STRUCTURE OF ALGAE CELLS

Prokaryotic algae are similar in cell structure to bacteria: they lack membrane organelles, such as a nucleus, chloroplasts, mitochondria, endoplasmic reticulum, and Golgi apparatus.

Eukaryotic algae contain structural elements characteristic of higher plant cells (Fig. 1).

Rice. 1. An adult plant cell without secondary wall thickening (schematized) at maximum magnification of a light microscope (by: 1 – cell wall, 2 – median plate, 3 – intercellular space, 4 – plasmodesmata, 5 – plasmalemma, 6 – tonoplast, 7 – central vacuole, 9 - nucleus, 10 - nuclear envelope, 11 - pore in the nuclear envelope, 12 - nucleolus, 13 - chromatin, 14 - chloroplast, 15 - grana in the chloroplast, 16 - starch grain in the chloroplast, 17 - mitochondrion, 18 - dictyosome, 19 – granular endoplasmic reticulum, 20 – droplet of reserve fat (lipid) in the cytoplasm, 21 – microbody, 22 – cytoplasm (hyaloplasm)

The above diagram of a plant cell generally reflects the structure of algae cells, however, many algae, along with typical plant organelles (plastids, vacuole with cell sap), contain structures characteristic of animal cells (flagella, stigma, membranes atypical for plant cells).

Cell covers

Cell covers ensure the resistance of the internal contents of cells to external influences and give the cells a certain shape. The covers are permeable to water and low molecular weight substances dissolved in it and easily transmit sunlight. The cell covers of algae are distinguished by great morphological and chemical diversity. They include polysaccharides, proteins, glycoproteins, mineral salts, pigments, lipids, and water. Unlike higher plants, there is no lignin in the shells of algae.

The structure of cell covers is based on the plasmalemma, or cytoplasmic membrane. In many flagellar and amoeboid representatives, the cells on the outside are covered only with plasmalemma, which is not capable of providing a constant body shape. Such cells can form pseudopodia. Based on morphology, several types of pseudopodia are distinguished. Most often found in algae rhizopodia, which are thread-like long, thin, branched, sometimes anastomosing cytoplasmic projections. There are microfilaments inside the rhizopodia. Lobopodia– wide rounded protrusions of the cytoplasm. They are found in algae with amoeboid and monadic types of thallus differentiation. Less common in algae filopodia- thin mobile formations resembling tentacles that can be retracted into the cell.

Many dinoflagellates have bodies covered with scales located on the surface of the cell. The scales can be single or close into a continuous cover - flowing. They may be organic or inorganic. Organic scales are found on the surface of green, golden, cryptophyte algae. The composition of inorganic flakes may include either calcium carbonate or silica. Calcium carbonate flakes – coccoliths– found predominantly in marine primnesiophyte algae.

Often, the cells of flagellated and amoeboid algae are located in houses that are mainly of organic origin. Their walls can be thin and transparent (genus Dinobryon) or more durable and colored due to the deposition of iron and manganese salts in them (genus Trachelomonas). The houses usually have one hole for the flagellum to exit, sometimes there may be several holes. When algae multiply, the house is not destroyed; most often, one of the resulting cells leaves it and builds a new house.

The cell covering of euglenoid algae is called a pellicle. The pellicle is a collection of the cytoplasmic membrane and the protein bands, microtubules and cisterns of the endoplasmic reticulum located under it.

In dinophyte algae, the cell covers are represented by amphiesma. Amphiesma consists of a plasmalemma and a set of flattened vesicles located under it, under which lies a layer of microtubules. The vesicles of a number of dinophytes may contain cellulose plates; this is called amphiesma current, or shell(birth Ceratium, Peridinium).

In diatoms, a special cell cover is formed on top of the plasmalemma - shell, consisting mainly of amorphous silica. In addition to silica, the shell contains an admixture of organic compounds and some metals (iron, aluminum, magnesium).

In the cell walls of green, yellow-green, red and brown algae, the main structural component is cellulose, which forms a framework (structural basis) immersed in a matrix (semi-liquid medium) consisting of pectin, hemicellulose, alginic acid and other organic substances.

Flagella

Monadic vegetative cells and monadic stages in the life cycle (zoospores and gametes) of algae are equipped with flagella - long and rather thick cell outgrowths, externally covered with plasmalemma. Their number, length, morphology, place of attachment, and pattern of movement are quite diverse in algae, but are constant within related groups.

The flagella may be attached at the anterior end of the cell (apical) or may be slightly moved to the side (subapical); they can be attached to the side of the cell (laterally) and on the ventral side of the cell (ventrally). Flagella identical in morphology are called isomorphic, if they differ - heteromorphic. Isocont- these are flagella of the same length, heterokontnye– different lengths.

Flagella have a single structure plan. One can distinguish the free part (undulipodium), transition zone, and basal body (kinetosome). Different parts of the flagellum differ in the number and arrangement of microtubules, which form the skeleton (Fig. 2).

Rice. 2. Scheme of the structure of algae flagella (according to: L.L. Velikanov et al., 1981): 1 – longitudinal section of the flagella; 2, 3 – transverse section through the tip of the flagellum; 4 – transverse section through the undulipodium; 5 – transition zone; 6 – cross section through the base of the flagellum – kinetosome

Undulipodium(translated from Latin as “wavepod”) is capable of making rhythmic wave-like movements. An undulipodium is a membrane-clad axoneme. Axoneme consists of nine pairs of microtubules arranged in a circle and a pair of microtubules in the center (Fig. 2). Flagella can be smooth or covered with scales or mastigonemes (hairs), and in dinophytes and cryptophytes they are covered with both scales and hairs. The flagella of prymnesiophyte, cryptophyte and green algae can be covered with scales of various shapes and sizes.

Transition zone. Functionally, it plays a role in strengthening the flagellum at the site of its exit from the cell. In algae, there are several types of transition zone structures: transverse plate (dinophytes), star-shaped structure (green), transition spiral (heterocontine), transition cylinder (primnesiophytes and dinophytes).

Basal body or kinetosome. This part of the flagellum has a structure in the form of a hollow cylinder, the wall of which is formed by nine triplets of microtubules. The function of the kinetosome is the connection of the flagellum with the plasmalemma of the cell. The basal bodies of a number of algae can take part in nuclear division and become centers of microtubule organization.

Mitochondria

Mitochondria are found in eukaryotic algae cells. The shape and structure of mitochondria in algae cells are more diverse compared to mitochondria of higher plants. They can be round, thread-like, network-shaped or irregular in shape. Their shape can vary in the same cell at different stages of the life cycle. Mitochondria are covered with a shell of two membranes. The mitochondrial matrix contains ribosomes and mitochondrial DNA. The inner membrane forms folds - cristas(Fig. 3).

Rice. 3. Structure of plant mitochondria (according to:): A – volumetric image; B—longitudinal section; B – part of the crista with mushroom-shaped protrusions: 1 – outer membrane, 2 – inner membrane, 3 – crista, 4 – matrix, 5 – intermembrane space, 6 – mitochondrial ribosomes, 7 – granule, 8 – mitochondrial DNA, 9 – ATP-somes

Algae cristae come in various shapes: disc-shaped (Euglenoid algae), tubular (Dinophyte algae), lamellar (green, red, cryptomonad algae) (Fig. 4).

Rice. 4. Different types of mitochondrial cristae (according to:): A – lamellar; B – tubular; B – disc-shaped; k - cristae

Disc-shaped cristae are considered the most primitive.

Pigments

All algae differ well in their set of photosynthetic pigments. Such groups in plant taxonomy have the status of divisions.

The main pigment of all algae is the green pigment chlorophyll. There are four known types of chlorophyll, which differ in their structure: chlorophylla– present in all algae and higher plants; chlorophyll b– found in green, charophyte, euglenoid algae and higher plants: plants containing this chlorophyll always have a bright green color; chlorophyll c– found in heterokont algae; chlorophyll d– a rare form, found in red and blue-green algae. Most photosynthetic plants contain two different chlorophylls, one of which is always chlorophyll a. In some cases, instead of the second chlorophyll, there are biliproteins. There are two types of biliproteins found in blue-green and red algae: phycocyanin– blue pigment, phycoerythrin- red pigment.

In addition to the listed pigments, algae also contain: fucoxanthin– golden pigment; xanthophyll- brown pigment.

Plastids

Pigments in the cells of eukaryotic algae are located in plastids, as in all plants. There are two types of plastids in algae: colored chloroplasts (chromatophores) and colorless leucoplasts (amyloplasts). The chloroplasts of algae, in contrast to those of higher plants, are much more diverse in shape and structure (Fig. 5).

Rice. 5. Scheme of the structure of chloroplasts in eukaryotic algae (by:): 1 – ribosomes; 2 – chloroplast shell; 3 – girdle thylakoid; 4 – DNA; 5 – phycobilisomes; 6 – starch; 7 – two membranes of chloroplast EPS; 8 – two membranes of the chloroplast shell; 9 – lamella; 10 – spare product; 11 – core; 12 – one membrane of chloroplast EPS; 13 – lipid; 14 – grain; 15 – pyrenoid. A – thylakoids are located one at a time, there is no CES - chloroplast endoplasmic reticulum (Rhodophyta); B – two-thylakoid lamellae, two CES membranes (Cryptophyta); B – trithylakoid lamellae, one CES membrane (Dinophyta. Euglenophyta); D – trithylakoid lamellae, two CES membranes (Heterokontophyta, Prymnesiophyta); D – two-, six-thylakoid lamellae, no CES (Chlorophyta)

The structural photosynthetic unit of eukaryotes and prokaryotes is thylakoid- flat membrane sac. Thylakoid membranes contain pigment systems and electron carriers. The light phase of photosynthesis is associated with thylakoids. The dark phase of photosynthesis takes place in the stroma of the chloroplast. The shell of green and red algae consists of two membranes. In other algae, the chloroplast is surrounded by an additional one or two membranes of the chloroplast endoplasmic reticulum(HES). In euglenaceae and most dinophytes, the chloroplast is surrounded by three membranes, and in heterokontaceae and cryptophytes - by four (Fig. 5).

Nucleus and mitotic apparatus

The algae nucleus has a structure typical of eukaryotes. The number of nuclei in a cell can vary from one to several. On the outside, the nucleus is covered with a shell consisting of two membranes; the outer membrane is covered with ribosomes. The space between nuclear membranes is called perinuclear. It may contain chloroplasts or leucoplasts, as in heterokonts and cryptophytes. The nuclear matrix contains chromatin, which represents DNA in complex with the main proteins - histones. The exception is the dinophytes, in which the number of histones is small and there is no nucleosomal chromatin organization. The chromatin threads of these algae are arranged in the form of figures of eight. There are from one to several nucleoli in the nucleus, which disappear or persist during mitosis.

Mitosis - indirect division of algae can occur in different ways, but in general the scheme of this process with 4 stages is preserved (Fig. 6).

Rice. 6. Consecutive phases of mitosis: 1 – interphase; 2-4 – prophase; 5 – metaphase; 6– anaphase; 7-9–telophase; 10– cytokinesis

Prophase– the longest phase of mitosis. The most important transformations take place in it: the nucleus increases in volume, instead of a barely noticeable chromatin network, chromosomes appear in it in the form of thin, long, curved and weakly spiraled threads, forming a kind of ball. From the very beginning of prophase, it is clear that chromosomes consist of 2 strands (the result of their replication in interphase). The halves of the chromosomes (chromatids) are located parallel to each other. As prophase develops, the threads become more and more spiralized, and the resulting chromosomes become increasingly shortened and compacted.

At the end of prophase, individual morphological characteristics of chromosomes are revealed. Then the nucleoli disappear, the nuclear membrane fragments into separate short cisterns, indistinguishable from the elements of the EPS, as a result of which the nucleoplasm is mixed with hyaloplasm and myxoplasm is formed; Achromatic filaments—the fission spindle—are formed from the substance of the nucleus and cytoplasm.

The fission spindle is bipolar and consists of bundles of microtubules stretching from one pole to the other. After the destruction of the nuclear membrane, each chromosome is attached to the spindle threads using its centromere. After chromosomes attach to the spindle, they line up in the equatorial plane of the cell so that all centromeres are at the same distance from its poles.

Metaphase. In this phase of mitosis, chromosomes reach maximum compaction and acquire a characteristic shape characteristic of each plant species. Usually they are double-armed, and in these cases, at the point of inflection, called centromere, chromosomes are connected to the achromatin filament of the spindle. In metaphase, it is clearly visible that each chromosome consists of two daughter chromatids. They are located more or less parallel in the equatorial plane of the cell. By the end of the stage, each chromosome is divided into two chromatids, which remain connected only at the centromere. Later, the centromeres also split into two sister ones; while sister centromeres and chromatids face opposite poles.

Anaphase. The shortest phase of mitosis. Daughter chromosomes - chromatids - diverge to opposite poles of the cell. Now the free ends of the chromatids are directed towards the equator, and the kinetochores - towards the poles. It is believed that the chromatids separate due to the contraction of the achromatin spindle filaments, which close to the centromere. Chromosomes become less noticeable due to unwinding and elongation. In the center of the cell (along the equator), sometimes already at this stage fragments of the cell wall - phragmoplast - appear.

Telophase. The process of unwinding continues - despiralization and elongation of chromosomes. Finally, they are lost in the field of view of the optical microscope. The nuclear membrane and nucleolus are restored. The same process occurs as in prophase, only in reverse order. Chromosomes now have one chromatid each. The structure of the interphase nucleus is restored, the spindle changes from a barrel-shaped to a cone-shaped one.

This is how it ends karyotomy– nuclear fission, then comes plasmatomy. Cytoplasmic organelles are distributed between the daughter cells, and some of them (dictyosomes, mitochondria and plastids) undergo significant modifications. Finally it happens cytokinesis– formation of a cell wall between daughter nuclei. From the previous cell two new ones were formed; each of them has a nucleus containing a diploid number of chromosomes.

Depending on the behavior of the nuclear membrane in algae, there are closed, semi-closed And open mitoses. In closed mitosis, chromosome segregation occurs without disruption of the nuclear membrane. In semi-closed mitosis, the nuclear envelope is maintained throughout mitosis, with the exception of the polar zones. In open mitosis, the nuclear membrane disappears in prophase. Depending on the shape of the spindle, divisions are distinguished pleuromitosis And orthomitosis.

In pleuromitosis, a metaphase plate does not form in metaphase and the spindle is represented by two half-spindles located at an angle to each other outside or inside the nucleus. During orthomitosis in metaphase, the chromosomes align with the equator of the bipolar spindle. Depending on the combination of these properties, the following types of mitosis are distinguished in algae (Fig. 7, 8):

Closed extranuclear mitosis

Closed intranuclear mitosis

Semi-closed mitosis

Open mitosis

Rice. 7. Scheme of the main types of mitoses in algae (according to: S.A. Karpov, year). Lines inside or outside the nucleus - spindle microtubules

The centers for organizing microtubules of the mitotic spindle in semi-closed orthomitosis can be kinetosomes and other structures:

– open orthomitosis, found in cryptophytes, goldensea, characeae;

– semi-closed orthomitosis, found in green, red, brown, etc.;

– closed orthomitosis, found in euglenoids;

– closed pleuromitosis, intranuclear or extranuclear, occurs in some dinophytes;

– semi-closed mitosis, during metaphase the centrioles are not at the poles, but in the region of the metaphase plate; can be observed in green trebuxiaceae.

Rice. 8. Diagram comparing (A) closed, (B) metacentric and (C) open mitoses (according to: L.E. Graham, L.W. Wilcox, 2000)

During mitosis, the shape of the spindle and the shape of the spindle poles also vary, as well as the duration of existence of the interzonal spindle. The peak of mitoses occurs during the dark period of the day. In multinucleated cells, nuclear division can occur synchronously. asynchronously, in waves.

Control questions

1. Name the main structural elements of plant cells.

2. The difference in the structure of algae cells from the cells of higher plants.

3. Cell covers of algae.

4. What is theca? In what algae is it found?

5. Main algae pigments. Location of pigments in algae cells.

6. Structure of plastids.

7. Structural features of algae plastids.

8. The structure of mitochondria.

9. Features of the structure of algae mitochondria.

10. Structure of the nucleus and nuclear membranes. Features of nuclear membranes in algae cells.

11. Scheme of mitosis. Characteristics of the phases of mitosis.

12. Types of mitosis in algae cells.

13. What is the difference between pleuromitosis and orthomitosis?

14. Types of algae pseudopodia.

2. GENERAL CHARACTERISTICS OF ALGAE

2.1. Power types

The main type of nutrition in algae is phototrophic type. In all departments of algae there are representatives that are strict (obligate) phototrophs. However, many algae quite easily switch from a phototrophic type of nutrition to the assimilation of organic substances, or heterotrophic food type. However, most often the transition to heterotrophic nutrition in algae does not lead to a complete cessation of photosynthesis, that is, in such cases we can talk about mixotrophic, or mixed type of nutrition.

The ability to grow on organic media in the dark or in light in the absence of carbon dioxide has been shown for many blue-greens, greens, yellow-greens, diatoms, etc. It has been noted that in algae, heterotrophic growth is slower than autotrophic growth in the light.

The diversity and plasticity of algae's feeding methods allows them to have a wide distribution and occupy various ecological niches.

2.2. Types of thalli

The vegetative body of algae is represented thallus, or thallus, not differentiated into organs - root, stem, leaf. Within the thallus structure, algae are distinguished by very large morphological diversity (Fig. 9). They are represented by unicellular, multicellular, and noncellular organisms. Their sizes vary widely: from the smallest single-celled organisms to giant multi-meter organisms. The body shape of algae is also diverse: from the simplest spherical to complexly dissected forms reminiscent of higher plants.

The huge variety of algae can be reduced to several types of morphological structure: monadic, rhizopodial, palmelloid, coccoid, trichal, heterotrichal, parenchymatous, siphonal, siphonocladal.

Monadic (flagellar) type of thallus structure

The most characteristic feature defining this type of structure is the presence of flagella, with the help of which monadic organisms actively move in the aquatic environment (Fig. 9, A). Motile flagellar forms are widespread in algae. Flagellate forms dominate among many groups of algae: euglenophytes, dinophytes, cryptophytes, raphidae, golden algae, and are found in yellow-green and green algae. Brown algae do not have a monadic type of structure in the vegetative state, but monadic stages are formed during reproduction (reproduction). The number of flagella, their length, the nature of placement and movement are varied and have important systematic significance.

Rice. 9. Morphological types of structure of thalli in algae (according to:): A– monadic ( Chlamydomonas); B– amoeboid ( Rhizochrisis); IN– palmelloid ( Hydrurus); G– coccoid ( Pediastrum); D– sarcinoid ( Chlorosarcina); E– filamentous ( Ulotrix); AND– multi-filamentous ( Fritchiela); Z, I– fabric ( Furcellaria, Laminaria); TO– siphonal ( Caulerpa); L– siphonocladal ( Cladophora)

The mobility of monad algae determines the polarity of the structure of their cells and colonies. Flagella are usually attached to the anterior pole of the cell or close to it. The basic shape of the cell is teardrop-shaped with a more or less narrowed anterior flagellar pole. However, monadic organisms often deviate from this basic shape and may be asymmetrical, spiral-shaped, have a tapered posterior end, etc.

The shape of the cell largely depends on the cell covers, which are very diverse (plasmalemma; pellicle; theca; consisting of organic, silica or calcareous scales; house; cell wall). The bizarre outlines of the cells of some golden algae form a kind of intracellular skeleton, consisting of hollow silica tubes. The cell membrane is usually smooth, sometimes bears various projections or is encrusted with iron or calcium salts and then resembles a house. Only small holes are formed in the shell for the exit of flagella.

The polarity of monadic organisms is also manifested in the arrangement of intracellular structures. At the anterior end of the cell there is often a variably arranged pharynx, usually performing an excretory function. Only a few phagotrophic flagellates have a pharynx that functions as a cell mouth - cytostome.

Peculiar organelles characteristic of algae having a monad structure are contractile vacuoles, performing an osmoregulatory function, mucous bodies And stinging structures. Stinging capsules are found in dinophyte, euglenoid, golden, raphidophyte, cryptophyte algae and perform a protective function. The single nucleus occupies a central position in the cells. Chloroplasts, varied in shape and color, can be axial or wall.

The tendency to increase body size is manifested in the formation of various colonies. In the simplest cases, colonies are formed due to nondisjunction of dividing cells. Colonies of ring-shaped, bushy, tree-like, and spherical shapes are observed. Green monadic organisms are mostly characterized by colonies of the type cenobians with a constant number of cells for each type.

Under unfavorable conditions, monadic organisms shed or retract their flagella, losing mobility, and surround themselves with abundant mucus.

The monadic type of structure turned out to be promising. On its basis, other, more complex structures developed.

Rhizopodial (amoeboid) type of structure

The most significant features of the amoeboid type of structure are the absence of strong cell covers and the ability to amoeboid movement, with the help of cytoplasmic outgrowths temporarily formed on the cell surface - pseudopodium. There are several types of pseudopodia, of which algae are most often observed rhizopodia And lodopodia, less often axopodia(Fig. 9, B).

There are no fundamental differences in the structure and mechanism of action of the contractile systems that determine the mobility of monadic and amoeboid organisms at the molecular level. The amoeboid movement probably arose as a result of the adaptation of flagellar cells to simplified living conditions, which led to a simplification of the body structure.

The cells of amoeboid algae contain nuclei, plastids, mitochondria and other organelles characteristic of eukaryotes: contractile vacuoles, stigma and basal bodies capable of forming flagella are often observed.

Many amoeboid organisms lead an attached lifestyle. They can build houses of various shapes and structures: thin, delicate, or rough, thick-walled.

The amoeboid body type is not as widespread as the monadic body type. It is observed only in golden and yellow-green algae.

Palmelloid (hemimonadal) type of structure

Characteristic of this type of structure is the combination of a stationary plant lifestyle with the presence of cellular organelles characteristic of monadic organisms: contractile vacuoles, stigma, flagella. Thus, vegetative cells may have flagella, with the help of which they move within the colonial mucus to a limited extent, or the flagella are preserved in immobile cells in a greatly reduced form.

Cells with the palmelloid (hemimonad) type are characterized by a polar structure. Sometimes the cages are located in houses.

Hemimonad algae often form colonies. In the simplest case, mucus is structureless, and the cells are located inside it in no particular order. Further complexity of such colonies is manifested both in the differentiation of mucus and in a more ordered arrangement of cells within the mucus. Colonies of the dendritic type (genus Hydrurus) (Fig. 9, IN).

The palmelloid (hemimonad) type of structure was an important stage in the morphological evolution of algae in the direction from mobile monadic to typically plant immobile forms.

Coccoid type of structure

This type combines unicellular and colonial algae, immobile in a vegetative state. Cells of the coccoid type are covered with a membrane and have a plant-type protoplast (tonoplast without contractile vacuoles, stigmas, flagella). The loss of signs of a monadic structure in the cell structure in organisms leading a plant-based, sedentary lifestyle, and the acquisition of new structures characteristic of plant cells is the next major step in the evolution of algae according to the plant type.

The huge variety of algae of the coccoid type of structure is associated with the presence of cell covers. The integument determines the presence of various cells: spherical, ovoid, fusiform, ellipsoidal, cylindrical, stellate-lobed, spiral, pear-shaped, etc. The variety of forms is also multiplied thanks to the sculptural decorations of the cell integument - spines, spines, bristles, horny processes.

Coccoid algae form colonies of various shapes, in which the cells are united with or without mucus.

The coccoid type of structure is widespread in almost all divisions of eukaryotic algae (with the exception of Euglenaceae).

In evolutionary terms, the cocoid structure can be considered as the initial one for the emergence of multicellular thalli, as well as siphonal and siphonocladal types of structure (Fig. 9, G, D).

Trichal (filamentous) type of structure

A characteristic feature of the filamentous type of structure is the filamentous arrangement of immobile cells, which are formed vegetatively as a result of cell division occurring predominantly in one plane. Filament cells have a polar structure and can grow only in one direction, coinciding with the axis of the nuclear spindle.

In the simplest cases, thalli of a filamentous structure are composed of cells that are morphologically similar to each other. At the same time, in many algae, in areas of the filaments that become thinner or wider towards the ends, the cells differ in shape from the rest. In this case, often the lower cell, devoid of chloroplasts, turns into a colorless rhizoid or foot. The threads can be simple or branching, single or multi-row, free-living or attached.

The filamentous type of structure is represented among green, red, yellow-green, and golden algae (Fig. 9, E).

Heterotrichal (non-filamentous) type of structure

The heterofilamentous type arose on the basis of the filamentous type. The heterofilamentous thallus consists mostly of horizontal threads creeping along the substrate, performing the function of attachment, and vertical threads rising above the substrate, performing the assimilation function. The latter bear the reproductive organs.

In some algae, vertical filaments are differentiated into internodes And nodes, from which whorls of lateral branches extend, which also have a segmented structure. In addition, additional threads can grow from the nodes, forming a crustal covering of the internodes. The function of attachment to the substrate is performed by colorless rhizoids. This structure can be found in charophytes, green, brown, red, some yellow-green and golden algae (Fig. 9, AND).

Parenchymal (tissue) type of structure

One of the directions in the evolution of the heterofilamentous thallus was associated with the emergence of parenchymatous thalli. The ability for unlimited growth and cell division in different directions led to the formation of voluminous macroscopic thalli with morphofunctional differentiation of cells depending on their position in the thallus (cortex, intermediate layer, pith).

Within this type, there is a gradual complication of thalli from simple plates to complex differentiated thalli with primitive tissues and organs. The parenchymal type of structure is the highest evolutionary stage of morphological differentiation of the algae body. It is widely represented in large algae: brown, red and green - the so-called macrophyte algae (Fig. 10).

Rice. 10. Cross section of the brown algae thallus (by:): 1 – outer bark; 2 – inner cortex; 3 – core

Siphonal type of structure

The siphonal (non-cellular) type of structure is characterized by the absence of cellular partitions inside the thallus, which reaches relatively large, usually macroscopic sizes and a certain degree of differentiation, in the presence of a large number of organelles. Partitions in such a thallus can appear only accidentally, when it is damaged, or during the formation of reproductive organs. In both cases, the process of formation of partitions differs from the formation of a multicellular organism.

The siphonal type of structure is present in some green and yellow-green algae. However, this direction of morphological evolution turned out to be a dead end.

Siphonocladal type of structure

The main feature of the siphonocladal type of structure is the ability to form complexly arranged thalluses, consisting of primarily multinucleated segments, from the primary noncellular thallus. The formation of such a thallus is based on segregation division, in which mitosis does not always end with cytokinesis.

The siphonocladal type of structure is known only in a small group of marine green algae.

2.3. Algae propagation

Reproduction is the main property of living beings. Its essence lies in reproducing its own kind. In algae, reproduction can be carried out asexually, vegetatively and sexually.

Asexual reproduction

Asexual reproduction of algae is carried out using specialized cells - dispute. Sporulation is usually accompanied by division of the protoplast into parts and the release of division products from the shell of the mother cell. Moreover, before the division of the protoplast, processes occur in it leading to its rejuvenation. The release of division products from the shell of the mother cell is the most significant difference between true asexual reproduction and vegetative reproduction. Sometimes only one spore is formed in a cell, but even then it leaves the mother shell.

Spores are usually produced in special cells called sporangia, differing from ordinary vegetative cells in size and shape. They arise as outgrowths of ordinary cells and perform only the function of forming spores. Sometimes spores are formed in cells that do not differ in shape and size from ordinary vegetative cells. Spores also differ from vegetative cells in shape and smaller size. The number of spores in a sporangium ranges from one to several hundred. Spores are a dispersal stage in the algal life cycle.

Depending on the structure there are:

zoospores– motile spores of green and brown algae, may have one, two, four or many flagella, in the latter case the flagella are located in a corolla at the front end of the spore or in pairs over the entire surface;

hemizoospores– zoospores that have lost flagella but retain contractile vacuoles and stigma;

aplanospores– non-motile spores that cover themselves with a membrane inside the mother cell;

motorsports– aplanospores, having the shape of a mother cell;

hypnospores– non-motile spores with thickened shells, designed to survive unfavorable environmental conditions.

In red algae, asexual reproduction occurs using monospore, bispor, tetraspore or polyspore. Monospores do not have a flagellum or membrane. After leaving the mother cell, they are capable of amoeboid movement. Monospores differ from vegetative cells by being ovoid or spherical in shape, rich in nutrients and intensely colored.

The structure of spores and types of sporulation are of great importance for the systematics of algae, since they reflect differences in the organization of the ancestral forms of various groups of algae.

Vegetative propagation

Vegetative propagation in algae can occur in several ways: simple division in two, multiple division, budding, fragmentation of the thallus, stolons, brood buds, paraspores, nodules, akinetes.

Simple division.

This method of reproduction is found only in unicellular forms of algae. Division occurs most simply in cells that have an amoeboid type of body structure.

Division of amoeboid forms. Amoeboid division is possible in any direction. It begins with the elongation of the amoeba's body, and then a partition is outlined at the equator, which divides the body into two more or less equal parts. The division of the cytoplasm is accompanied by division of the nucleus. Sometimes division is preceded by a transition to a stationary state due to the retraction of the legs, and the cell acquires a spherical shape. At the same time, the protoplasm loses its transparency and the contractile vacuole disappears. Towards the end of division, the cell is stretched, laced, and then pseudopods appear.

Division of flagellated forms. In flagellated forms, the most complex types of vegetative propagation occur. Types of reproduction are determined by the level of organization and the degree of cell polarity. In some cryptophyte, golden and green algae, reproduction by simple division in two occurs in a mobile state only along the longitudinal axis and begins from the anterior pole of the cell. In this case, the flagella can go to only one cell or be equally divided between new cells. A cell that does not have a flagellum forms one itself. In most Volvox and Euglena algae, during reproduction, the cell membrane becomes mucus and division occurs in a stationary state. In all flagellated forms that have a shell, the cells are divided into two equal or unequal parts. After separation, the old shell is shed and a new one is formed.

Division of coccoid forms. In algae with a coccoid type of cell structure, vegetative reproduction acquires the typical features of division of a stationary plant cell with a well-defined cell wall. In its simplicity, it approaches the amoeboid type of vegetative reproduction and is carried out by simple division of the cell in two.

Budding.

Cells of filamentous branched algae are characterized by two ways of vegetative reproduction: simple division in two and budding. The combination of these methods of reproduction causes lateral branching of filamentous algae.

Fragmentation.

Fragmentation is inherent in all groups of multicellular algae and manifests itself in different forms: the formation of hormogonium, regeneration of detached parts of the thallus, spontaneous loss of branches, regrowth of rhizoids. The cause of fragmentation may be mechanical factors (waves, currents, animal gnawing), or the death of some cells. An example of the latter method of fragmentation is the formation of hormogonia in blue-green algae. Each hormogonium can give rise to a new individual. Reproduction by parts of thalli, characteristic of red and brown algae, does not always lead to the resumption of normal plants. Seaweed growing on rocks and rocks is often partially or completely destroyed by wave action. Their detached fragments or entire thalli are not able to re-attach themselves to solid soils due to the constant movement of water. In addition, the attachment organs are not formed again. If such thalli find themselves in quiet places with a muddy or sandy bottom, they continue to grow while lying on the ground. Over time, the older parts die off and the branches extending from them turn into independent thalli; in such cases they speak of unattached, or free-living, forms of the corresponding species. The algae change greatly: their branches become thinner, narrower and branch weaker. Unattached forms of algae do not form organs of sexual and asexual reproduction and can only reproduce vegetatively.

Reproduction by shoots, stolons, brood buds, nodules, akinetes.

In the tissue forms of green, brown and red algae, vegetative reproduction takes on its complete form, which differs little from the vegetative reproduction of higher plants. While retaining the ability to regenerate parts of the thallus, tissue forms acquire specialized formations that perform the function of vegetative propagation. Many species of brown, red, green and chara algae have shoots on which new thalli grow. On the thalli of some brown and red algae, brood buds (propagules) develop, which fall off and grow into new thalli.

With the help of unicellular or multicellular overwintering nodules, seasonal renewal of charophytic algae occurs. Some filamentous algae (for example, green ulothrix algae) reproduce by akinetes - specialized cells with a thickened shell and a large amount of reserve nutrients. They are able to survive adverse conditions.

Sexual reproduction

Sexual reproduction in algae is associated with the sexual process, which consists of the fusion of two cells, resulting in the formation of a zygote that grows into a new individual or produces zoospores.

There are several types of sexual reproduction in algae:

hologamy(conjugation) – without the formation of specialized cells;

gametogamy– with the help of specialized cells – gametes.

Hologamy. In the simplest case, the process occurs by the fusion of two immobile vegetative cells lacking cell membranes. In unicellular flagellated forms of algae, the sexual process is carried out by the fusion of two individuals.

When the contents of two flagellated vegetative cells merge, the sexual process is called conjugation. During conjugation, the fusion of two cells occurs, which perform the function of germ cells - gametes. The fusion of cell contents occurs through a specially formed conjugation channel, resulting in a zygote, which is subsequently covered with a thick membrane and turns into a zygospore. If the rate of flow of cell contents is the same, a zygote is formed in the conjugation channel. In this case, the division of cells into male and female is conditional.

Gametogamy. Sexual reproduction in algae, including unicellular algae, most often occurs by dividing the contents of the cells and the formation of specialized germ cells in them - gametes. In all green and brown algae, male gametes have flagella, but female gametes do not always have them. In primitive algae, gametes are formed in vegetative cells. In more highly organized forms, gametes are located in special cells called gametangia. A vegetative cell or gametangium can contain from one to several hundred gametes. Depending on the size of the merging gametes, several types of gametogamy are distinguished: isogamy, heterogamy, oogamy.

If the merging gametes have the same shape and size, this sexual process is called isogamy.

If the merging gametes have the same shape, but different sizes (the female gamete is larger than the male one), then they speak of heterogamy.

A sexual process in which an immobile large cell merges - egg and a mobile small male cell - sperm, called oogamy. Gametangia with eggs are called archegonia or oogonia, and with spermatozoa – antheridia. Male and female gametes can develop on the same individual (monoecious) or on different individuals (dioecious). The zygote formed as a result of the fusion of gametes, after some changes, turns into a zygospore. The latter is usually covered with a dense shell. Zygospore can remain dormant for a long time (up to several months) or germinate without a dormant period.

Autogamy. A special type of sexual process. It consists in the fact that the cell nucleus divides meiotically, of the four nuclei formed, two are destroyed, and the remaining two nuclei merge, forming a zygote, which, without a rest period, increases in size and turns into an auxospore. This is how individuals rejuvenate.

2.4. Life cycles of algae

Life cycle, or development cycle, is a set of all stages of development of organisms, as a result of which, from certain individuals or their rudiments, new individuals and rudiments similar to them are formed. The stage of aging, leading to the death of the individual, and periods of rest extend beyond the life cycle. The development cycle can be simple or complex, which is associated with the ratio of diploid and haploid nuclear phases, or forms of development(Fig. 11).

Rice. 11. Life cycles of algae (according to:): I – haplobiont with zygotic reduction; II – haplodiplobiont with sporic reduction; III – diplobiont with gametic reduction; IV – haplodiplobiont with somatic reduction. The dominant phase in cases I and III is multicellular; if it is unicellular, then it is long-lasting and capable of mitotic reproduction; 1 – haploid phase; 2 – diploid phase

The concept of life cycle is associated with the alternation of generations. Under generation understand the totality of individuals considered in relation to ancestors and descendants living at a close time, and genetically related to it.

A simple life cycle is characteristic of cyanobacteria, in which sexual reproduction is not found. Their life cycles are complete ( big) And small. The small life cycle corresponds to certain branches of the large cycle and leads to the repeated formation of intermediate age states of cyanobacteria individuals . The development cycle of cyanobacteria, thus, includes certain segments of the development of one or a number of successive generations of a specific systematic form: from the primordium of an individual to the emergence of new primordia of the same type.

In most algae with a sexual process, depending on the time of year and external conditions, different forms of reproduction are observed (sexual and asexual), with a change in the haploid and diploid nuclear phases. The changes undergone by an individual between the same phases of development constitute his life cycle.

Organs of sexual and asexual reproduction can develop on the same individual or on different individuals. Plants that produce spores are called sporophytes, and the forming gametes are gametophytes. Plants that can produce both spores and gametes are called gametosporophytes. Gametosporophytes are characteristic of many algae: green (Ulvacaceae), brown (Ectocarpaceae) and red (Bangieaceae). The development of reproductive organs of one type or another is determined by the temperature of the environment. For example, on the lamellar thalli of red algae Porphyra Tenera at temperatures below 15–17 °C, organs of sexual reproduction are formed, and at higher temperatures, organs of asexual reproduction are formed. In general, in many algae, gametes develop at a lower temperature than spores. The development of certain reproductive organs is also influenced by other factors: light intensity, day length, chemical composition of water, including its salinity.

Gametophytes, gametosporophytes and sporophytes of algae may not differ in appearance or have well-defined morphological differences. Distinguish isomorphic(similar) and heteromorphic(different) changes in forms of development, which are identified with the alternation of generations. In most gametosporophytes, alternation of generations does not occur. Sometimes gametophytes and sporophytes, without differing morphologically, exist in different environmental conditions; in some cases they differ morphologically. For example, in red algae Porphyra Tenera sporophytes have the form of branching single-row filaments that are embedded in the calcareous substrate (mollusk shells, rocks). They grow preferentially in low light and penetrate the substrate to great depths. The gametophytes of this algae have the form of plates and grow in good light near the water's edge and in the tidal zone.

With heteromorphic alternation of generations, the structure of sporophytes and gametophytes differs in some cases quite significantly. Thus, in green algae from the genera Acrosiphony And Spongomorpha the gametophyte is multicellular, several centimeters high, and the sporophyte is unicellular, microscopic. Other ratios of gametophyte and sporophyte sizes are also possible. In brown algae Sugars the gametophyte is microscopic, and the sporophyte is up to 12 m long. In most algae, gametophytes and sporophytes are independent plants. In a number of species of red algae, sporophytes grow on gametophytes, and in some brown algae, gametophytes develop inside the sporophyte thallus.

A heteromorphic change in developmental forms, when a clearly defined separation of the sporophyte from the gametophyte is observed, is characteristic of more highly organized groups of algae. In this case, one of the forms, most often the gametophyte, is microscopic. It is believed that the heteromorphic development cycle of algae arose from an isomorphic one. The methods of development of the gametophyte and sporophyte are of great importance in the taxonomy of algae. The most complex and diverse development cycles, not found in other algae, are characteristic of red algae.

Change of nuclear phases.

During the sexual process, as a result of the fusion of gametes and their nuclei, the number of chromosomes in the nucleus doubles. At a certain stage of the development cycle, during meiosis, the number of chromosomes is reduced, as a result of which the resulting nuclei receive a single set of chromosomes. The sporophytes of many algae are diploid, and meiosis in their development cycle coincides with the moment of formation of spores, from which haploid gametosporophytes or gametophytes develop. This meiosis is called sporic reduction. Sporophytes of more primitive red algae (genera Cladophora, Ectocarpus and many others) along with haploid spores form diploid spores, which again develop into sporophytes. Spores appearing on gametosporophytes serve for self-renewal of mother plants. Sporophytes and gametophytes of algae at the highest stages of evolution strictly alternate without self-renewal.

In a number of algae, meiosis occurs in the zygote. This meiosis is called zygotic reduction and is found in a number of species of green and charophyte algae. In freshwater volvox and ulothrix algae, the sporophyte is represented by a unicellular zygote, which produces up to 32 zoospores, the mass of which is many times greater than the parent gametes, i.e. essentially a sporic reduction is observed.

Some groups of algae have gametic reduction, which is characteristic of animals, and not of plant organisms. In these algae, meiosis occurs during the formation of gametes, while the remaining cells of the thallus remain diploid. Such a change in nuclear phases is inherent in diatoms and brown fucus algae, which are widespread throughout the globe (which include the most widespread species of marine algae), and among green algae, in the large genus Cladophora. Development with gametic reduction of the nucleus is believed to give these algae certain advantages over others.

If reduction division occurs in sporangia before the formation of spores of asexual reproduction (sporic reduction), then there is an alternation of generations - a diploid sporophyte and a haploid gametophyte. This type of life cycle is called haplobiont with sporic reduction. It is characteristic of some green algae, many brown and red algae.

Finally, in a few algae, meiosis occurs in the vegetative cells of the diploid thallus (somatic reduction), from which haploid thalli then develop. Such life cycle with somatic reduction known from red and green algae.

Control questions

Types of algae nutrition.

Types of algae thallus.

Characteristics of the monadic morphological structure.

Characteristics of rhizopodial morphological structure. Types of cytoplasmic processes.

Characteristics of palmelloid morphological structure.

Characteristics of coccoid morphological structure.

Characteristics of the trichal morphological structure.

Characteristics of heterotrichal morphological structure.

Characteristics of parenchymal morphological structure.

Characteristics of the siphonal morphological structure.

Characteristics of siphonocladal morphological structure.

12. Asexual reproduction. Types of disputes.

13. Types of vegetative propagation of algae.

14. Types of sexual reproduction of algae.

15. How do sporophytes and gametophytes differ?

16. What is heteromorphic and isomorphic change of generations?

17. Change of nuclear phases in the life cycle of algae. Sporical, zygotic and gametic reduction.

3. ECOLOGICAL GROUPS OF ALGAE

Algae are distributed throughout the globe and are found in various aquatic, terrestrial and soil biotopes. Various ecological groups are known: algae of aquatic habitats, terrestrial algae, soil algae, algae of hot springs, algae of snow and ice, algae of hypersaline springs.

3.1. Algae of aquatic habitats

3.1.1. Phytoplankton

The term “phytoplankton” means a collection of plant organisms floating in the water column. Planktonic algae are the main, and in some cases the only, producer of primary organic matter, on the basis of which all life in a body of water exists. The productivity of phytoplankton depends on a complex of various factors.

Planktonic algae live in a variety of bodies of water - from the ocean to a puddle. Moreover, the greater diversity of environmental conditions in inland water bodies compared to the seas also determines a significantly greater diversity of species composition and ecological complexes of freshwater plankton.

Phytoplankton of freshwater ecosystems characterized by a clearly defined seasonality. In each season, one or several groups of algae predominate in a reservoir, and during periods of intensive development, often only one species dominates. So in winter, under the ice (especially when the ice is covered with snow), phytoplankton is very poor or almost absent due to lack of light. The vegetative development of plankton algae as a community begins in March - April, when the level of sunlight becomes sufficient for photosynthesis of algae even under ice. At this time, quite numerous small flagellates appear - euglenophytes, dinophytes, golden ones, as well as cold-loving diatoms. During the period of ice breaking up before temperature stratification is established, which usually happens when the upper layer of water is heated to 10–12C°, the rapid development of the cold-loving complex of diatoms begins. In summer, when the water temperature is above 15C°, the maximum productivity of blue-green, euglenoid and green algae is observed. Depending on the trophic and limnological type of the reservoir, water “blooming” may occur at this time, caused by the development of blue-green and green algae.

One of the significant features of freshwater phytoplankton is the abundance of temporary planktonic algae in it. A number of species, which are generally considered to be typically planktonic, in ponds and lakes have a bottom or periphyton (attached to some object) phase in their development.

Marine phytoplankton consists mainly of diatoms and dinophytes. Of the diatoms, representatives of the genera are especially numerous Chaetoceros, Rhizosolenia, Thalassiosira and some others absent from freshwater plankton. The composition of flagellar forms of dinophyte algae in marine phytoplankton is very diverse. Representatives of primnesiophytes are very numerous in marine phytoplankton; they are represented in fresh waters by only a few species. Although the marine environment is relatively homogeneous over large areas, similar homogeneity is not observed in the distribution of marine phytoplankton. Differences in species composition and abundance are often pronounced even in relatively small areas of sea water, but they are especially clearly reflected in the large-scale geographic zonality of distribution. Here the ecological effect of the main environmental factors is manifested: water salinity, temperature, light and nutrient content.

Planktonic algae usually have special adaptations for living in suspension. Some have various kinds of outgrowths and body appendages - spines, bristles, horny outgrowths, membranes. Others form colonies that secrete mucus abundantly. Still others accumulate substances in their bodies that increase their buoyancy (droplets of fat in diatoms, gas vacuoles in blue-greens). These formations are much more developed in marine phytoplankters than in freshwater ones. One of the adaptations for existing suspended in the water column is the small body size of planktonic algae.

3.1.2. Phytobenthos

Phytobenthos refers to a set of plant organisms that are adapted to exist in an attached or unattached state at the bottom of reservoirs and on various objects, living and dead organisms in water.

The possibility of benthic algae growing in specific habitats is determined by both abiotic and biotic factors. Among biotic factors, competition with other algae and the presence of consumers play a significant role. This leads to the fact that certain types of benthic algae do not grow at all depths and not in all water bodies with suitable light and hydrochemical conditions. Light is especially important for the growth of benthic algae as photosynthetic organisms. But the degree of its use is influenced by other environmental factors: temperature, content of biogenic and biologically active substances, oxygen and inorganic carbon sources, and most importantly, the rate of entry of these substances into the thallus, which depends on the concentration of substances and the speed of water movement. As a rule, places with intense water movement are characterized by lush development of benthic algae.

Benthic algae growing in active conditions water movement, gain advantages over algae growing in sedentary waters. The same level of photosynthesis can be achieved by phytobenthos organisms under flow conditions with less light, which promotes the growth of larger thalli. The movement of water, moreover, prevents the settling of silt particles on rocks and stones, which interfere with the fixation of algae buds, favor the growth of bottom algae, washing away algae-eating animals from the soil surface. Finally, although during strong currents or strong surf the algae thalli are damaged or torn from the ground, the movement of water still does not prevent the settlement of microscopic species of algae or microscopic stages of macrophyte algae.

The influence of water movement on the development of benthic algae is especially noticeable in rivers, streams and mountain streams. In these reservoirs there is a group of benthic organisms that prefer places with strong currents. In lakes where there are no strong currents, wave motion becomes of primary importance. In the seas, waves also have a significant impact on the life of benthic algae, in particular on their vertical distribution.

In the northern seas, the distribution and abundance of benthic algae is influenced by ice. Depending on its thickness, movement and hummocking, algae thickets can be destroyed (erased) to a depth of several meters. Therefore, for example, in the Arctic, perennial brown algae ( Fucus, Laminaria) is easiest to find near the shore among boulders and rock ledges that impede the movement of ice.

The life of benthic algae is influenced in many ways by temperature. Along with other factors, it determines their growth rate, the pace and direction of development, the moment of formation of their reproductive organs, and the geographic zonality of distribution.

Intensive development of algae is also facilitated by moderate content in water. nutrients. In fresh waters, such conditions are created in shallow ponds, in the coastal zone of lakes, in river backwaters, in the seas - in small bays.

If in such places there is sufficient lighting, hard soils and weak water movement, then optimal conditions for the life of phytobenthos are created. In the absence of water movement and its insufficient enrichment with nutrients, benthic algae grow poorly. Such conditions exist in rocky bays with a large bottom slope and significant depths in the center, since nutrients from bottom sediments are not carried into the upper horizons. In addition, macroscopic seaweeds, which serve as substrates for many small forms of benthic algae, may be absent in such habitats.

Sources of nutrients in water are coastal runoff and bottom sediments. The role of the latter is especially great as accumulators of organic residues. In bottom sediments, as a result of the vital activity of bacteria and fungi, mineralization of organic residues occurs; complex organic substances are converted into simple inorganic compounds available for use by photosynthetic plants.

In addition to light, water movement, temperature and nutrient content, the growth of benthic algae depends on presence of herbivorous aquatic animals– sea urchins, gastropods, crustaceans, fish. This is especially noticeable in the thickets of kelp algae, which are large in size. In tropical seas, in some places, fish completely eat up green, brown and red algae with a soft thallus. Gastropods, crawling along the bottom, eat microscopic algae and small seedlings of macroscopic species.

The predominant bottom algae of continental water bodies are diatoms, green, blue-green and yellow-green filamentous algae, attached or not attached to the substrate.

The main benthic algae of the seas and oceans are brown and red, sometimes green, macroscopic attached thallous forms. All of them can be overgrown with small diatoms, blue-green and other algae.

Depending on the place of growth, the following ecological groups are distinguished among benthic algae:

epiliths– grow on the surface of hard soil (rocks, stones);

epipelites– inhabit the surface of loose soils (sand, silt);

epiphytes– epizoites– live on the surface of plants/animals;

endophytes– endozoites or endosymbionts– live inside the body of plants/animals, but feed independently (have chloroplasts and photosynthesize);

endoliths– live in calcareous substrate (rocks, mollusk shells, crustacean shells).

Sometimes a group of organisms is isolated fouling, or periphyton. Organisms included in this group live on objects that are mostly moving or flown around by water. In addition, they are removed from the bottom and are exposed to different light, food and temperature conditions than truly bottom-dwelling organisms.

The fouling composition includes microalgae and macrophyte algae. Microscopic algae (blue-green and diatoms) form a mucous bacterial-algal-detrital film on a substrate introduced into the aquatic environment. Then macroalgae (red, brown and green) settle on the primary microfilm along with the animals. This creates serious interference in human economic activity. Due to fouling, the speed of ships and the efficiency of hydroacoustic devices decreases, fuel consumption increases, and underwater structures become heavier and corrode. In addition, the slimy film formed by fouling can disrupt the operation of water pipes, clog the openings of water intakes and pipelines, and disrupt heat exchange processes in refrigeration units.

Attached fouling organisms that live on underwater structures in the intertidal zone and at depths of up to 1 m are usually eliminated in winter by prolonged drying and abrasion by ice. Therefore, every year in the spring-summer period, fouling communities are formed here, characteristic of the pioneer stage of biological succession. The dominant species of such communities, along with barnacles and mollusks, are often macrophyte algae. In the sublittoral zone of underwater structures - from a depth of 0.7-0.9 m to their base (6-12 m) - perennial fouling develops. Its composition is dominated by brown algae from the genera Saccharina And Costaria. The biomass of these large algae in temperate latitudes can be very significant, amounting to tens of kilograms per square meter.

Fouling algae can also exist in the air ( aerophyton). Of these, green and blue-green algae predominate. Under certain conditions, aerophyton algae can damage industrial and building materials, architectural monuments, paintings, etc., if they are not protected by toxic coatings. The cause of damage is the metabolic products of fouling agents, mainly organic acids. Aerophyton algae are especially common in the humid tropics, where there is enough heat, moisture and dust of organic origin, which is a breeding ground for their development. Biodamage from them can be significant.

Epilites. This group includes attached algae. They populate the surface of stones, forming crust-like coverings or flat pads, or have special attachment organs - rhizoids. Intensive development of epiliths is observed in reservoirs with a hard bottom and fast flowing water. Typical epiliths are representatives of golden algae from the genus Hydrurus, brown algae from the genera Saccharina, Kelp, Costaria and etc.

Epipelites. Loose algae spreading along the bottom, binding and strengthening the substrate. They are often represented by diatoms, aureus, euglenoids, cryptophytes, and dinophytes freely crawling on the substrate. The attachment organs of epipelites are sometimes short rhizoids that cannot take deep root. Only charophyte algae with their long rhizoids develop well on muddy bottoms.

Usually, the organs of attachment of epiliths and epipeliths are special formations - sole, leg, foot, mucous cord or mucous pad, cushion, etc.

Epiphytes/epizoites. Algae use living organisms as a substrate. Epizoites are algae that settle on animals. On the surface of mollusk shells there are small green ( Edogonium, Cladophora, Ulva) and red ( Gelidium, Palmaria,) seaweed; on sponges - green, blue-green and diatoms. Epizoites live on crustaceans, rotifers, less commonly on aquatic non-insects or larvae, worms and even larger animals. Epizoites include species of green and charophyte algae from the genera Chlorangiella, Charatiochloris, Korzhikoviella, Chlorangiopsis etc. Most epizoites cannot exist in isolation from the substrate. Algae usually die on dead animals or on their shells shed during molting.

Epiphytes are algae that live on plants. Short-term connections arise between the substrate plant (basiphyte) and the epiphyte plant. The complex and interesting phenomenon of epiphytism is still poorly understood. There are frequent cases of double or even triple epiphytism, when some algae settling on other, larger forms themselves are a substrate for other, smaller or microscopic species. Sometimes the physiological state of the substrate plant is important for the development of epiphytes. The number of epiphytes, as a rule, increases as the basifite algae ages. For example, the greatest species richness of epiphytic aedogonia algae is observed on dead aquatic plants ( Manna, Reed, Sedge).

Endophytes/endozoites, or endosymbionts

Endosymbionts, or intracellular symbionts - algae that live in the tissues or cells of other organisms (invertebrate animals or algae). They form a kind of ecological group. Intracellular symbionts do not lose the ability to photosynthesize and reproduce inside host cells. A variety of algae can be endosymbionts, but the most numerous are endosymbioses of unicellular green and yellow-green algae with unicellular animals. The algae participating in such symbioses are respectively called zoochlorella And zooxanthellae. Green and yellow-green algae form endosymbioses with multicellular organisms: sponges, hydras, etc. Endosymbioses of blue-green algae with protozoa are called syncyanoses. Often, other types of cyanobacteria can settle in the mucus of some blue-green species. They usually use ready-made organic compounds, which are formed in abundance during the breakdown of the mucus of the colony of the host plant, and multiply intensively.

The most common endophytes are representatives of goldens (species of the genera Chromulina, Myxochloris) and green (genus Chlorochitrium, Chlamydomyx) algae that settle in the body of duckweed and sphagnum mosses. Green algae genus Carteria settles in the epidermal cells of the ciliated worm Convolute, one species of the genus Chlorella– in the vacuoles of protozoa, and species of the genus Chlorococcum– in the cells of cryptophyte algae Cyanophora.

3.1.3. Algae of extreme aquatic ecosystems

Hot spring algae. Algae that grow at temperatures of 35–85 °C are called thermophilic. Often, high environmental temperatures are combined with a high content of mineral salts or organic substances (heavily contaminated hot wastewater from factories, factories, power plants or nuclear plants). Typical inhabitants of hot waters are blue-green algae and, to a lesser extent, diatoms and green algae.

Algae of snow and ice. Algae that grow on the surface of ice and snow are called cryophilic. When developing in large numbers, they can cause green, yellow, blue, red, brown or black “blooming” of snow or ice. Among cryophilic algae, green, blue-green and diatom algae predominate. Only a few of these algae have dormant stages; most lack any special morphological adaptations to tolerate low temperatures.

Algae from salt water bodies got the name halophilic or halobionts. Such algae grow at high salt concentrations in water, reaching 285 g/l in lakes with a predominance of table salt and 347 g/l in Glauberian lakes. As salinity increases, the number of algae species decreases; Only a few of them can tolerate very high salinity. In oversaline (hyperhaline) water bodies, unicellular mobile green algae predominate - hyperhalobes, whose cells lack a membrane and are surrounded by plasmalemma ( Asteromonas, Pedinomonas). They are distinguished by an increased content of sodium chloride in the protoplasm, high intracellular osmotic pressure, and the accumulation of carotenoids and glycerol in the cells. In some settled reservoirs, such algae can cause red or green “blooming” of the water. The bottom of hyperhaline reservoirs is sometimes completely covered with blue-green algae; Among them, species from the genera predominate Oscillatorium, Spirulina etc. With a decrease in salinity, an increase in the species diversity of algae is observed: in addition to blue-green algae, diatoms appear (species of the genera Navicula, Nietzsche).

3.2. Algae of non-aquatic habitats

Although the main living environment for most algae is water, due to the eurytopic nature of this group of organisms, they successfully colonize a variety of out-of-water habitats. In the presence of at least periodic moisture, many of them develop on various ground objects - rocks, tree bark, fences, etc. A favorable habitat for algae is soil. In addition, communities of endolith algae are also known, the main living environment of which is the surrounding calcareous substrate.

Communities formed by algae in extra-aquatic habitats are divided into aerophilic, edaphilic and lithophilic.

3.2.1. Aerophilic algae

The main living environment of aerophilic algae is the air surrounding them. Typical habitats are the surface of various extra-soil hard substrates (rocks, stones, tree bark, house walls, etc.). Depending on the degree of moisture, they are divided into two groups: air and water-air. Air algae They live in conditions of only atmospheric moisture and experience a constant change in humidity and drying. Water-air algae are exposed to constant irrigation with water (under the spray of waterfalls, in the surf zone, etc.).

The living conditions of these algae are very peculiar and are characterized, first of all, by the frequent change of two factors - humidity and temperature. Algae that live in conditions of exclusively atmospheric moisture are often forced to transition from a state of excessive moisture (for example, after a rainstorm) to a state of minimal moisture during dry periods, when they dry out so much that they can be ground into powder. Aquatic algae live in conditions of relatively constant moisture, however, they also experience significant fluctuations in this factor. For example, algae that live on rocks irrigated by the spray of waterfalls experience a moisture deficit in the summer, when the flow decreases significantly. Aerophilic communities are also susceptible to constant temperature fluctuations. They get very hot during the day, cool down at night, and freeze in winter. True, some aerophilic algae live in fairly constant conditions (on the walls of greenhouses). But in general, relatively few algae, represented by microscopic unicellular, colonial and filamentous forms of blue-green and green algae and, to a much lesser extent, diatoms, have adapted to the unfavorable conditions of existence of this group. Aerophilic forms are also known among red algae of the genus Porphyridium and etc.; they are found on stones and old walls of greenhouses. The number of species found in aerophilic groups approaches 300. When aerophilic algae develop in mass quantities, they usually take the form of powdery or slimy deposits, felt-like masses, soft or hard films and crusts.

On the bark of trees, the usual settlers are the ubiquitous green algae from the genera Pleurococcus, Chlorella, Chlorococcus. Blue-green algae and diatoms are found much less frequently on trees. There is evidence that predominantly green algae grow on gymnosperms.

The systematic composition of algae groups living on the surface of exposed rocks is different. Diatoms and some, mostly unicellular, green algae develop here, but representatives of blue-green algae are most common in these habitats. Algae and accompanying bacteria form “mountain tan” (rock films and crusts) on crystalline rocks of various mountain ranges. The debris that accumulates in rock recesses is usually inhabited by single-celled green algae and blue-green algae. Algae growths are especially abundant on the surface of wet rocks. They form films and growths of various colors. As a rule, species equipped with thick mucous membranes live here. Depending on the light intensity, the mucus can be colored more or less intensely, which determines the color of the growths. They can be bright green, golden, brown, purple, almost black, depending on the species that form them. Particularly characteristic of irrigated rocks are representatives of blue-green algae, such as species of the genera Gleocapsa, Tolipothrix, Spirogyra etc. In the growths on wet rocks you can also find diatoms from the genera Frustulia, Akhnantes and etc.

Thus, aerophilic algae communities are very diverse and arise both under completely favorable and extreme conditions. External and internal adaptations to this lifestyle are varied and similar to the adaptations of soil algae, especially those developing on the soil surface.

3.2.2. Edaphilic algae

The main living environment of edaphophilic algae is soil. Typical habitats are the surface and thickness of the soil layer, which has a physical and chemical effect on the bionts. Depending on the location of algae and their lifestyle, three groups are distinguished within this type: terrestrial algae, massively developing on the soil surface under atmospheric moisture conditions; water-terrestrial seaweed, developing en masse on the surface of the soil, constantly saturated with water; soil algae, inhabiting the thickness of the soil layer.

Soil as a biotope is similar to both aquatic and aerial habitats: it contains air, but it is saturated with water vapor, which ensures breathing with atmospheric air without the threat of drying out. Property. which fundamentally distinguishes the soil from the above-mentioned biotopes is its opacity. This factor has a decisive influence on the development of algae. However, in the soil thickness, where light does not penetrate, viable algae are found at a depth of up to 2 m in virgin lands and up to 2.7 m in arable lands. This is explained by the ability of some algae to switch to heterotrophic nutrition in the dark.

A small number of algae are found in the deep layers of the soil. To maintain their viability, soil algae must have the ability to tolerate unstable humidity, sudden temperature fluctuations and strong insolation. These properties are ensured by a number of morphological and physiological features. For example, it has been noted that soil algae are relatively small in size compared to the corresponding aquatic forms of the same species. As cell size decreases, their water-holding capacity and resistance to drought increase. An important role in the drought resistance of soil algae is played by the ability to produce abundant mucus - slimy colonies, covers and wrappers consisting of hydrophilic polysaccharides. Due to the presence of mucus, algae quickly absorb water when moistened and store it, slowing down drying. Soil algae stored in an air-dry state in soil samples demonstrate amazing viability. If such soil is placed on a nutrient medium after decades, it will be possible to observe the development of algae.

A characteristic feature of soil algae is the “ephemerality” of the growing season - the ability to quickly move from a state of dormancy to active life and vice versa. They are also able to withstand temperature fluctuations over a very wide range: from -200 to +84°C. Soil algae (mostly blue-green) are resistant to ultraviolet and radioactive radiation.

The vast majority of soil algae are microscopic forms, but they can often be seen on the soil surface with the naked eye. The massive development of such algae can cause greening of the slopes of ravines and the sides of forest roads.

In terms of systematic composition, soil algae are quite diverse. Among them, blue-green and green algae are represented in approximately equal proportions. Yellow-green algae and diatoms are less diverse in the soils.

3.2.3. Lithophilic algae

The main living environment of lithophilic algae is the opaque dense calcareous substrate surrounding them. Typical habitats are deep within hard rocks of a certain chemical composition, surrounded by air or submerged in water. There are two groups of lithophilic algae: drilling algae, which actively penetrate into the limestone substrate; tuff-forming algae, depositing lime around their body and living in the peripheral layers of the environment they deposit, within the limits accessible to water and light. As sediment builds up, it dies off.

Control questions

1. Describe the main ecological groups of algae in aquatic habitats: phytoplankton and phytobenthos.

2. Differences between freshwater and marine phytoplakton. Representatives of marine and freshwater phytoplankton.

3. Morphological adaptations of algae to the planktonic lifestyle.

4. Seasonal changes in qualitative and quantitative indicators of freshwater phytoplankton.

5. Differences between freshwater and marine phytobenthos. Systematic composition of marine and freshwater phytobenthos.

6. Ecological groups of phytobenthos in relation to the substrate (epilites, epipelites, epiphytes, endophytes).

7. What is fouling? What algae can make up this ecological group?

8. Aerophilic algae. Adaptations to extreme environmental conditions. Systematic composition of aerial algae.

9. Edaphilic algae. Adaptations to environmental conditions. Systematic composition of soil algae.

10. Lithophilic algae.

4. ROLE OF ALGAE IN NATURE AND PRACTICAL IMPORTANCE

The role of algae in natural ecosystems. In aquatic biocenoses, algae play the role of producers. Using light energy, they are able to synthesize organic substances from inorganic ones. According to radiocarbon dating, the average primary production of the oceans due to the vital activity of algae is 550 kg of carbon per 1 hectare per year. The total value of its primary production is 550.2 billion tons (in raw biomass) per year and, according to scientists, the contribution of algae to the total production of organic carbon on our planet ranges from 26 to 90%. Algae play an important role in the nitrogen cycle. They are able to use both organic (urea, amino acids, amides) and inorganic (ammonium and nitrate ions) sources of nitrogen. A unique group are blue-green algae, which are capable of fixing nitrogen gas, converting it into compounds available to other plants.

Algae - oxygen producers. Algae, in the process of their life activity, release oxygen necessary for the respiration of aquatic organisms. In the aquatic environment (especially in the seas and oceans), algae are practically the only producers of free oxygen. In addition, they play a large role in the overall oxygen balance on Earth, since the oceans serve as the main regulator of the oxygen balance in the Earth's atmosphere.

Algae are a medium for other aquatic organisms. By forming underwater forests, macrophyte algae create highly productive ecosystems that provide food, shelter and protection to many other living organisms. It was established that a column of water with a volume of 5 liters containing one specimen of brown algae Cystoseira contains up to 60 thousand individuals of various invertebrate animals, including mollusks, mites and crustaceans.

Algae - pioneers of vegetation. Terrestrial algae can settle on bare rocks, sand and other barren places. After they die, the first layer of future soil is formed. Soil algae participate in the processes of formation of soil structure and fertility.

Algae as a geological factor. The development of algae in past geological epochs has led to the formation of a number of rocks. Together with animals, algae took part in the formation of reefs in the oceans. Settled closer to the surface of the water, they formed the ridges of these reefs. Reef structures of red algae are known in the Crimea as the peaks of Yayla and others. Blue-green algae participated in the formation of stromatolite limestones, chara algae - in the formation of charocyte limestones (similar deposits were found in Tuva). Cocolithophores take part in the formation of Cretaceous rocks (Cretaceous rocks are 95% composed of the remains of the shells of these algae). The massive accumulation of diatom shells led to the formation of diatomite (mountain flour), large deposits of which were discovered in the Primorsky Territory, the Urals and Sakhalin. Algae were the starting material for liquid and solid petroleum-like compounds - sapropels, hot shale, coal.

The active activity of algae in the formation of rocks has been noted in some regions at the present time. They absorb calcium carbonate and form mineralized products. These processes are especially active in tropical waters with high temperatures and low partial pressure.

Boring algae are of greatest importance in the destruction of rocks. They slowly and persistently loosen calcareous substrates, making them available for weathering, crumbling and erosion.

Symbiotic relationships with other organisms. Algae form several important symbioses. Firstly, they form lichens with fungi, and secondly, as zooxants they live together with some invertebrate animals, such as sponges, ascidians, and reef corals. A number of cyanophytes form associations with higher plants.

Algae are of great practical importance in everyday life and human economic activity, bringing both benefit and harm. Large, mainly seaweeds have been known since ancient times and have long been used in human agriculture.

Algae as a food product. Humans eat mainly seaweed; they are especially widely used by residents of Southeast Asia and the Pacific Islands. In China, the use of algae in the diet has been known since the 9th century BC. e. Among macrophyte algae (multicellular green, brown and red) there are no poisonous species, because they do not contain alkaloids - substances with a narcotic and poisonous effect. About 160 species of different algae are used for food. In terms of nutritional qualities, algae are not inferior to many agricultural crops. They contain a large percentage of protein, carbohydrates and fats. Algae are an excellent source of vitamins C, A, D, group B, riboflavin, pantothenic and folic acids, and microelements.

Of microscopic algae, blue-green terrestrial species of the genus are used as food. Nostok, which serve as food in China and South America. In Japan, they eat barley bread "tengu" - these are thick layers of dense gelatinous mass on the slopes of some volcanoes, consisting of blue-green algae from the genera Gleocapsa, Geoteke, Microcystis with an admixture of bacteria. Spirulina used by the Aztecs back in the 16th century, preparing cakes from dried seaweed, and the population of the Lake Chad region in North America still prepares a product called dihe from this seaweed. Spirulina contains high amounts of protein and is widely cultivated in a number of countries.

Algae as fertilizer. Algae contain a sufficient amount of organic and mineral substances, so they have long been used as fertilizers. The advantages of such fertilizers are that they do not contain weed seeds and spores of phytopathogenic fungi, and their potassium content is superior to almost all types of fertilizers used. Nitrogen-fixing blue-green algae are widely used in rice fields instead of nitrogen fertilizers. It has been shown that algae fertilizers can increase seed germination, yield, and disease resistance.

Medicinal properties of algae. Algae are widely used in folk medicine as an anthelmintic and for the treatment of a number of diseases, such as goiter, nervous disorders, sclerosis, rheumatism, rickets, etc. It has been shown that extracts of many types of algae contain antibiotic substances and can reduce blood pressure. Extracts from Sargassum, Kelp and Saharina in experiments on mice, they suppressed the growth of sarcoma and leukemic cells. In the USA and Japan, drugs have been obtained from them that help remove radionuclides from the body. The efficiency of such sorbents reaches 90–95%.

Algae as a source of industrial raw materials. Since the last century, algae have been used to produce soda and iodine. Currently, alginic acid and its salts - alginates, as well as carrageenans and agar are obtained from algae.

Mannitol alcohol is obtained from brown algae - a necessary raw material for the pharmaceutical and food industries in the manufacture of medicines and food products for diabetics.

Negative role of algae. A number of algae (blue-green, dinophyte, golden, green) produce toxins that can cause various diseases in animals, plants and humans, some of which can be fatal. Among the dinophyte algae that cause “red tides” in vast marine areas, the species of the genera are toxic Gymnodinium, Noctiluca, Amphidinium etc. The largest number of toxic species was identified among blue-green algae. The action of blue-green algae toxins is several times greater than that of poisons such as curare and botulin. The toxicity of algae manifests itself in the mass death of aquatic organisms, waterfowl, poisoning and other diseases of people that occur through inhalation, use of water, consumption of shellfish, fish, etc.

With strong development - “blooming of water bodies”, some algae (golden, yellow-green, blue-green) can give the water an unpleasant odor and taste, making the water unsuitable for drinking.

Excessive algae growth can prevent water from passing through the filters of water intake structures. It is known that algae fouling of ships significantly increases operating costs. Macrophytes can contribute to the corrosion of materials on oil platforms and other underwater marine structures.

The problem of fouling is perhaps the oldest problem in ocean exploration. Any object that comes into contact with the marine environment is soon covered with a mass of organisms attached to it: animals and algae. The total area of submerged substrates is about 20% of the surface area of the upper shelf. The total biomass of fouling amounts to millions of tons, the damage from it amounts to billions of dollars (Zvyagintsev, 2005). In the biological aspect, this is a natural process that forms an integral part of the life of the hydrosphere. At the same time, the phenomenon of fouling suggested to man the idea of growing a number of valuable species of mollusks in marine fisheries on an industrial scale ( Oysters, Mussels, Scallops, Pearl mussels) and algae ( Saccharines, Porphyry, Gracilaria, Euchema and etc.). Algae are pioneer fouling organisms. Microalgae, together with bacteria, form a primary microfilm on the surface of artificial substrates added to water, which serves as a substrate for the sedimentation of other hydrobionts. Macroalgae, together with crustaceans, mollusks, hydroids and other animals, often form the initial stages of perennial fouling communities.

Control questions

1. The role of algae in increasing land fertility.

2. The role of algae in aquatic ecosystems.

3. The role of algae in terrestrial ecosystems.

4. The importance of algae in geological processes.

5. Nutritional and biological value of algae. What seaweed can be eaten?

6. Medicinal properties of algae.

7. Why is the growth of golden and yellow-green algae in reservoirs undesirable? What is “blooming” of water bodies?

8. Algae that cause poisoning of animals and humans.

9. Fouling phenomenon. The role of algae in fouling communities.

5. MODERN SYSTEMATICS OF ALGAE

The classification of living organisms has occupied the minds of people since the time of Aristotle. The Swedish botanist Carl Linnaeus was the first to apply the name Algae to a group of plants in the 18th century and began phycology(from Greek phycos – algae and logos – teaching) as a science. Among algae, Linnaeus distinguished only four genera: Chara, Fucus, Ulva and Conferva. In the 19th century, the majority (several thousand) of modern algae genera were described. The large number of new genera necessitated grouping them into higher-ranking taxa. Initial attempts at classification were based solely on external features of the thallus. The first to propose the color of algae thallus as a fundamental character for the establishment of large taxonomic groups, or megataxa, was the English scientist W. Harvey (Harvey, 1836). He identified large series: Chlorospermeae - green algae, Melanospermeae - brown algae and Rhodospermeae - red algae. They were later renamed Chlorophyceae, Phaeophyceae, and Rhodophyceae, respectively.

The foundations of modern algae taxonomy were laid in the first half of the 20th century by the Czech scientist A. Pascher. He established 10 classes of algae: Blue-green, Red, Green, Golden, Yellow-green, Diatom, Brown, Dinophyte, Cryptophyte and Euglenaceae. Each class is characterized by a specific set of pigments, reserve products and the structure of flagella. These constant differences between large taxa prompted us to consider them as independent phylogenetic groups, unrelated, and to abandon the concept of algae - Algae as a specific taxonomic unit.

Thus, the word “algae” is actually not a systematic, but an ecological concept and literally means “what grows in water.” Algae are lower plants that contain the vast majority of chlorophyll, are capable of phototrophic nutrition and live primarily in water. All algae, except charophytes, unlike higher plants, do not have multicellular reproductive organs with covers of sterile cells.

Modern systems differ mainly in the number and volume of megataxa - divisions and kingdoms. The number of departments varies from 4 to 10-12. In Russian phycological literature, almost each of the above classes corresponds to a department. In foreign literature, there is a tendency towards consolidation of departments and, accordingly, a decrease in their number.

The most common in classification schemes is Parker's scheme (Parker, 1982). It recognizes the division between prokaryotic and eukaryotic forms. Prokaryotic forms do not have membrane-surrounded organelles in their cells. Prokaryotes include Bacteria and Cyanophyta (Cyanobacteria). Eukaryotic forms include all other algae and plants. The algae division has long been a subject of debate. Harvey (1836) divided algae primarily by color. Although many more divisions are now recognized, the composition of pigments, biochemical and structural features of the cell structure are given great importance. P. Silva (1982) distinguishes 16 main classes. The classes differ in pigmentation, storage products, cell wall features and ultrastructure of flagella, nucleus, chloroplasts, pyrenoids and ocelli.

New information on the ultrastructure of algae, obtained in recent decades using the methods of electron microscopy, genetics and molecular biology, makes it possible to study the smallest details of the cell structure. “Explosions” of information periodically prompt scientists to reconsider established traditional ideas about the taxonomy of algae. The constant flow of new information stimulates new approaches to classification, and each proposed scheme inevitably remains approximate. According to modern data, organisms traditionally considered among lower plants go beyond the scope of the Plant Kingdom. They are included in a large number of independently evolving groups. The table shows megataxa, which include algae, in different interpretations. As can be seen, different algal taxa can be found in different phyla; the same phyla can unite different ecological and trophic groups of organisms (table).

More than 100 years ago K.A. Timiryazev perspicaciously noted that “there is neither plant nor animal, but there is one inseparable organic world. Plants and animals are only average values, only typical ideas that we form, abstracting from the known characteristics of organisms, attaching exceptional importance to some, neglecting others.” Now we can't help but admire his amazing biological intuition.

The modern algae system outlined in this textbook includes 9 divisions: Blue-green, Red, Diatoms, Heterokonts, Haptophytes, Cryptophytes, Dinophytes, Green, Charophytes and Euglenophytes. The similarity in the composition of pigments, the structure of the photosynthetic apparatus and flagella served as the basis for uniting the classes of algae with a golden-brown color into one large group - Heterokontae, or heteroflagellate algae (Ochrophyta).

Megasystem of organisms classified as lower plants

Empire	Kingdom	Department (Type)	Trophogroup
Eubacteria/Prokaryota	Cyanobacteria/Bacteria	Cyanophyta/ Cyanobacteria	Seaweed
Excavates/Eukaryota	Euglenobiontes/ Protozoa	Euglenophyta/ Euglenozoa Acrasiomycota	Seaweed Myxomycetes
Rhizaria/Eukaryota	Cercozoa/ Plantae	Chlorarachniophyta Plasmodiophoromy-cota	Algae Myxomycetes
Rhizaria/Eukaryota		Myxogasteromycota Dictyosteliomycota	Myxomycetes Myxomycetes
Choromalveola-tes/ Eukaryota	Straminopilae/ Chromista/ Heterokontobiontes	Labyrinthulomycota -Oomycota Heterokontophyta	Myxomycetes Fungi Algae
Choromalveola-tes/ Eukaryota	Haptophytes/ Chromista	Prymnesiophyta/Haptophyta	Seaweed
Choromalveola-tes/ Eukaryota	Cryptophytes/ Chromista		Seaweed
Choromalveola-tes/ Eukaryota	Alveolates/Protozoa	Dinophyta/Myzozoa	Seaweed
Plantae/ Eukaryota	Glaucophytes/ Plantae	Glaucocystophyta/ Glaucophyta	Seaweed
Plantae/ Eukaryota	Rhodobiontes/ Plantae	Cyanidiophyta Rhodophyta	Algae Algae
Plantae/ Eukaryota	Chlorobiontes/ Plantae	Chlorophyta Charophyta	Algae Algae