Crustaceans- These are aquatic arthropods or inhabitants of wet places. Their body sizes vary from a few millimeters to 1 m. They are ubiquitous; lead a free or attached lifestyle. The class includes about 20 thousand species. Only crustaceans are characterized by the presence of two pairs of antennae, biramous limbs, and gill breathing. The class Crustacea combines 5 subclasses. Conventionally, all representatives are divided into lower (daphnia, cyclops) and higher crayfish (lobster, spiny lobster, shrimp, crayfish).
Representative of higher cancers - river crayfish. It lives in fresh water bodies with running water, is nocturnal and is a predator.
Crayfish. External and internal structure:
1 - Antennae, 2 - Claw, 3 - Walking legs, 4 - Caudal fin, 5 - Abdomen, 6 - Cephalothorax, 7 - Head ganglion, 8 - Digestive tube, 9 - Green gland, 10 - Gills, 11 - Heart, 12 - gonad
The body of the cancer is covered with a dense chitinous shell. The fused segments of the head and chest form the cephalothorax. Its front part is elongated and ends with a sharp spike. Two pairs of antennae are located in front of the spine, and two complex (faceted) eyes are located on the sides on movable stalks. Each eye contains up to 3 thousand small eyes. Modified limbs (6 pairs) form the oral apparatus: the first pair is the upper jaws, the second and third are the lower jaws, the next three pairs are the jaws. The thoracic region bears 5 pairs of jointed limbs. The first pair is the organ of attack and defense. It ends with powerful pincers. The remaining 4 pairs are walking limbs. The limbs of the jointed abdomen are used in females for carrying eggs and cubs. The abdomen ends with a caudal fin. When the crayfish swims, it scoops up water with it and moves with its tail end forward. Bundles of striated muscles are attached to the internal protrusions of the chitinous cover.
Cancer feeds on both living organisms and decaying animal and plant debris. The crushed food enters through the mouth into the pharynx and esophagus, then into the stomach, which has two sections. Chitinous teeth of the chewing section grind food; in the filter stomach, it is filtered and enters the middle intestine. The ducts of a large digestive gland, which performs the functions of the liver and pancreas, also open here. Under the action of its secret, the food slurry is digested. Nutrients are absorbed, and undigested residues through the hindgut and anus are thrown out.
The excretory organs of cancer are a pair of green glands (modified metanephridia) that open at the base of long antennae. Respiratory organs - gills located on the sides of the cephalothorax. They are permeated with blood vessels in which gas exchange occurs - the blood gives off carbon dioxide and is saturated with oxygen. The circulatory system is not closed. It consists of a pentagonal heart located on the dorsal side and vessels extending from it. The blood pigment contains copper, which is why it is blue in color. The nervous system of crayfish resembles the nervous system of annelids. It consists of the supraglottic and subpharyngeal ganglia, united in the circumpharyngeal ring, and the ventral nerve cord. The organs of vision, touch and smell (on the antennae), balance (at the base of the short antennae) are well developed. Cancers are segregated. Reproduction is sexual, development is direct. Eggs are laid in winter; small crayfish hatch from eggs in early summer. Cancer expresses concern for offspring.
Significance of crustaceans. Crustaceans serve as food for aquatic animals and for humans (lobsters, crabs, shrimps, crayfish). They clean the water bodies from carrion. Some representatives of crustaceans cause diseases of fish, settling on their skin or gills, some are intermediate hosts for tapeworms and roundworms.
Crustaceans are a large class of arthropods. The most famous representatives of this group are crayfish, shrimps, lobsters, lobsters, crabs, krill. All of them have a strong chitinous skeleton (cuticle) in which the bodies of animals are enclosed.
Because of this external skeleton, growth of crustaceans, like all arthropods, occurs only in short intervals between molts. During molting, the cuticle in which the animal is located bursts, and the animal crawls out of it, like out of old clothes.
Within a few days or hours until the new cuticle is soft and rapid growth occurs. Then the cuticle becomes hard and the body no longer grows. At an early age, when the animal develops, molts occur frequently. Adult crustaceans molt less frequently. A detailed video lesson on the structure of crustaceans.
marine crustaceans
Crustaceans live in both fresh and salt water bodies: seas and salt lakes. Marine crustaceans are known to us in greater numbers than freshwater ones, because we most often eat them.
The inhabitants of the sea coasts know a variety - crabs and hermit crabs, which can be observed directly in their natural habitat - water. For example, in Primorsky Krai in all bays and on all beaches on a rocky bottom, the most popular crab is an ordinary coastal crab. It got its name because it lives in close proximity to the coast and does not descend to depths of more than 10 m.
Shellfish, video:
The main character of this video is a Far Eastern representative of crustaceans - an ordinary coastal crab.
higher and lower crustaceans
The class of crustaceans is divided into two groups (two subclasses) - lower and higher crustaceans:
- the body of lower crustaceans in different species consists of a different number of segments (sectors) - from 10 to 46;
- the body of higher crustaceans always has the same number of segments - 18 (head - 4, chest - 8 and abdomen -6);
The common coastal crab is a typical representative of higher crustaceans. If we turn it over, we will see the abdomen bent under the shell and count 6 segments in it.
Legs of crustaceans
Let's continue our acquaintance with higher crustaceans - a detachment of decapods, which includes the common coastal crab.
The thoracic region of the crab has 8 pairs of limbs;
- 3 front pairs of thoracic limbs are turned into jaw legs and participate in food retention;
- The remaining 5 pairs are walking legs that serve directly for the movement of the crab;
- The 1st pair of walking legs has claws and serves to grasp and crush prey;
So, higher crustaceans have 5 pairs of legs, of which the first pair is equipped with claws.
stalked eyes of crustaceans
There are two types of crustacean eyes:
- unpaired frontal (nauplis) eye, consisting of 3-4 eye cups;
- a pair of compound (faceted) eyes, each of which consists of numerous small eyes (sometimes there are up to 3000 of them);
In the coastal crab, about which you watched the video, compound paired eyes sit on movable outgrowths of the head - stalks. This gives him the ability to see everything that is happening around him. Watch the video again and pay attention to the crab's stalked eyes.
So, it was an article in the rubric and a very brief acquaintance with the class of crustaceans - with some features of their structure.
Latin name Crustacea
Characteristics of crustaceans
The subphylum Gillbreathers contains one class of crustaceans (Crustacea), richly represented in the modern fauna. They are characterized by the presence of two pairs of head antennae: antennules and antennae.
Dimensions crustaceans range from fractions of a millimeter in microscopic planktonic forms to 80 cm in higher crustaceans. Many crustaceans, especially planktonic forms, serve as food for commercial animals - fish and whales. Other crustaceans themselves serve as the subject of fishing.
Body dismemberment
The body of crustaceans is segmented, but, unlike annelids, their segmentation is heteronomous. Similar segments that perform the same function are combined into departments. In crustaceans, the body is divided into three sections: the head (cephalon), chest (thorax) and abdomen (abdomen). The head of crustaceans is formed by an acron corresponding to the head lobe - the prostomium of annelids, and four trunk segments merged with it. Accordingly, the head section bears five pairs of head appendages, namely: 1) antennules - single-branched tactile antennae innervated from the brain (homologous to the palps of the annulus); 2) antennae, or second antennae, originating from the first pair of biramous limbs of the parapodial type; 3) mandibles, or mandibles, - upper jaws; 4) first maxillae, or first pair of lower jaws; 5) second maxillae, or second pair of lower jaws.
However, not all crustaceans have acron and the four segments that form the head are fused together. In some lower crustaceans, the acron is fused with the antennal segment, but does not merge with the independent mandibular segment, but both maxillary segments are fused together. The anterior part of the head, formed by the acron and the segment of the antennae, is called the primary head, the protocephalon. In many crustaceans (except for the formation of the primary head - the protocephalon), all the jaw segments (the mandibular and both maxillary) also merge to form the jaw section - the gnathocephalon. This section fuses with a greater or lesser number of thoracic segments (in crayfish with three thoracic segments), forming the jaw-thorax - gnathothorax.
In many, the head consists of five completely merged parts: an acron and four body segments (shields, cladocerans, some amphipods, and isopods), and in some, the head segments merge with one or two more thoracic segments (copepods, isopods, amphipods).
In many, the dorsal integuments of the head form an outgrowth at the back, more or less covering the thoracic region, and sometimes the entire body. This is how the cephalothoracic shield, or carapace, of crayfish and other decapods is formed, and the transverse groove on this shell indicates the border between the merged jaw and thoracic parts of the body. The carapace grows to the thoracic segments. Sometimes it can be compressed from the sides, forming a gable shell that hides the entire body (shellfish).
The thoracic segments, as indicated, can grow together with the head (1-3, even 4 segments), forming a cephalothorax. All thoracic segments bear limbs whose functions are not limited to motor and respiratory. So, in crayfish 3, the first pairs of thoracic limbs turn into mandibles, which provide food to the mouth.
The abdominal segments are usually movably connected to each other. Only the higher crustaceans have limbs on the abdominal segments; the rest of the abdomen is devoid of them. The abdominal region ends in a telson, which does not bear limbs and is homologous to the pygidium of polychaetes.
While in all crustaceans the number of head segments is the same (5), the number of thoracic and abdominal segments is very different. Only in higher crayfish (decapods, isopods, etc.) their number is constant: thoracic - 8, abdominal - 6 (rarely 7). In the rest, the number of thoracic and abdominal segments ranges from 2 (shellfish) to 50 or more (shields).
limbs
The limbs of the head are represented by five pairs. Antennules corresponding to the palps of the annulus retain in crustaceans mainly the functions of the sense organs - touch and smell. Antennules of crayfish consist of main segments and two segmented branches.
The antennae are the first pair of limbs of parapodial origin. In the larvae of many crustaceans, they are biramous, while in most adult crayfish they become single-branched or retain only a rudiment of the second branch (exopod). Antennas perform mainly a tactile function.
The mandibles make up the upper jaws. They correspond in origin to the second pair of limbs. In most crayfish, the mandibles are turned into hard jagged chewing plates (mandibles) and have completely lost their biramous character. It is believed that the chewing plate corresponds to the main part of the limb - the protopodite. In crayfish (and some others), a small three-segmented palp sits on the chewing plate - the remnant of one of the branches of the limb.
The first and second maxillae, or the first and second pairs of mandibles, are usually less reduced limbs than the mandibles. In decapods, the maxillae consist of two main segments, forming a protopodite, and a short, unbranched palp. With the help of the chewing plate of the protopodite, the maxillae perform the chewing function.
The thoracic limbs of representatives of different orders are arranged differently. In crayfish, the first three pairs of thoracic limbs are transformed into the so-called mandibles or maxillopods. The maxillae of the crayfish, especially the second and third pairs, retain a fairly strong biramous structure (endopodite and exopodite). The second and third pairs also bear gills, and their movement causes currents of water through the gill cavity. Therefore, they perform a respiratory function. However, their main function is to hold food and move it to the mouth. Finally, the endopod of the third pair serves as a kind of toilet device, with the help of which the antennules and eyes are cleaned of foreign particles adhering to them.
However, in many other crustaceans, the first three pairs of thoracic limbs perform a predominantly locomotor function.
A peculiar change in the thoracic limbs is their adaptation to grasping, for example, the claws of decapod crayfish. The claw is formed by two limb segments: the penultimate segment, which has a long outgrowth, and the last segment articulated with it, forming the other side of the claw. Fifth - eighth pairs of thoracic limbs of crayfish (and other decapods) are typical walking legs. They are single-branched, and their basal part (protopodite) and endopodite are preserved. The exopod is completely reduced. Two-branching of the thoracic limbs is observed much more often in lower crustaceans.
Abdominal limbs, as already mentioned, are absent in many groups of crustaceans. In higher crustaceans, they are usually less developed than thoracic ones, but more often they remain biramous; in many crayfish they are equipped with gills, simultaneously performing a respiratory function. In crayfish, the abdominal legs - pleopods - are changed in males. Their first and second pairs represent the copulatory apparatus. In females, the first pair is rudimentary. The second - the fifth pair of abdominal legs in females and the third - the fifth pair in males of the swimming type. They are biramous and consist of few segments, abundantly covered with hairs. The eggs laid by the crayfish females are attached to these legs, which they bear, and then the hatched crustaceans hold on to the legs of the female for some time.
The last, sixth pair of abdominal legs - uropods - is peculiarly changed in crayfish and in some other crayfish. Both branches of each leg are turned into flat swimming lobes, which, together with the flat last segment of the abdomen - the telson - form a fan-shaped swimming apparatus.
In crabs, an interesting protective adaptation is often observed - spontaneous discarding of limbs, sometimes occurring even with very little irritation. This autotomy (self-mutilation) is associated with a strong ability to regenerate. A new limb develops in place of the lost limb.
Skeleton and muscles
The chitinized cover is impregnated with calcium carbonate. This gives greater rigidity to the skeleton.
The mobility of the body and limbs in the presence of a hard cover is ensured by the fact that chitin covers the body and limbs with a layer of unequal thickness and hardness. Each segment of the crayfish abdomen is covered with hard plates of chitin on the dorsal and ventral sides. The dorsal shield is called tergite, the abdominal shield is called sternite. On the boundaries between the segments, the boggy and soft chitin forms folds, which straighten when the body is bent in the opposite direction. A similar adaptation is observed on the joints of the limbs.
The internal skeleton of the cancer serves as an attachment site for various muscles. In many places, especially on the ventral side of the thoracic region, the skeleton forms a complex system of crossbars that grow inside the body and form the so-called endophragmal skeleton, which also serves as a site of muscle attachment.
All sorts of bristles, hairs covering the body of the cancer, and especially its limbs, are outgrowths of the chitinous cover.
Digestive system
The digestive system is represented by the intestine, which consists of three main sections: the anterior, middle and hindgut. The anterior and posterior intestines are of ectodermic origin and are internally lined with a chitinous cuticle. Crustaceans are characterized by the presence of a paired digestive gland, usually called the liver. The digestive system reaches its greatest complexity in decapod crayfish.
The anterior intestine of crayfish is represented by the esophagus and stomach. The mouth is located on the ventral side, a short esophagus extends upwards from it to the dorsal side. The latter leads to the stomach, which consists of two sections - cardiac and pyloric. The cardial, or chewing, section of the stomach is lined from the inside with chitin, which forms a complex system of crossbars and protrusions equipped with teeth in its back. This formation is called the "gastric mill", it provides the final grinding of food. In front of the cardial section, white rounded limestone formations are placed - millstones. Calcium carbonate, which accumulates in them, is used during molting to impregnate the new chitinous cover with it. Food crushed in the cardial part of the stomach enters through a narrow passage into the second, pyloric part of the stomach, in which the food particles are pressed and filtered. This part of the stomach ensures that only highly crushed food enters the middle intestine and the digestive gland. It must be borne in mind that not only mechanical grinding of food takes place in the stomach, but also partly its digestion, since the secret of the digestive gland penetrates into the stomach. The remaining unground larger food particles, due to the special structure of the pyloric part of the stomach, pass directly into the hindgut, bypassing the midgut, and are brought out.
The midgut of crayfish is very short. It is approximately 1/20 of the entire length of the intestine. Digestion and absorption of food takes place in the midgut. Most of the liquid food from the stomach goes directly to the digestive gland (liver), which opens with two openings at the border of the midgut and the pyloric part of the stomach. Digestive enzymes that digest proteins, fats, and carbohydrates are not only excreted into the midgut and stomach, but are also used in the liver tubules themselves. Liquid food penetrates into these tubes, and here its final digestion and absorption takes place.
In many crustaceans, the digestive gland is much less developed (for example, in daphnia), and in some it is completely absent (in cyclops). In such crustaceans, the midgut is relatively longer.
The hindgut is a straight tube lined with chitin from the inside and opens with an anus on the ventral side of the telson.
Respiratory system
Most crustaceans have special respiratory organs - gills. By origin, the gills develop from the epipodites of the limbs and, as a rule, are located on the protopodites of the thoracic, less often ventral, legs. In a simpler case, the gills are plates sitting on the protopodite (amphibians, etc.); in a more perfect form, the gills are a rod seated with thin gill filaments. The lacunae of the body cavity - the mixocoel - go inside the gills. Here they form two channels, separated by a thin partition: one - bringing, the other - taking out.
In decapods, including crayfish, the gills are placed in special gill cavities formed by the lateral folds of the cephalothoracic shield. In crayfish, the gills are arranged in three rows: the lower row is located on the protopodites of all thoracic limbs, the middle row is located at the places where the limbs are attached to the cephalothorax, and the upper row is located on the side wall of the body. In crayfish, 3 pairs of mandibles and 5 pairs of walking legs are equipped with gills. Water constantly circulates in the gill cavities, getting there through holes at the base of the limbs, in places where the folds of the cephalothoracic shield do not fit tightly to them, and exits at its front edge. The movement of water is due to the rapid oscillatory movements of the second maxillae and partly of the first pair of maxillae.
Crustaceans that have passed to terrestrial existence have special adaptations that provide breathing with atmospheric air. In land crabs, these are modified gill cavities, in wood lice - limbs pierced by a system of air tubes.
Many small forms (copepods, etc.) do not have gills and respiration is carried out through the integument of the body.
Circulatory system
Due to the presence of a mixed body cavity - the mixocoel - the circulatory system is open and the blood circulates not only through the blood vessels, but also in the sinuses, which are sections of the body cavity. The degree of development of the circulatory system varies and depends on the development of the respiratory system. It is most developed in higher crustaceans, especially in decapods, which, in addition to the heart, have a rather complex system of arterial vessels. In other crustaceans, the vascular system is much less developed. Daphnia has no arterial vessels at all and the circulatory system is represented only by the heart in the form of a bubble. Finally, copepods and barnacles also lack a heart.
The heart of crustaceans, tubular or sac-shaped, is placed on the dorsal side of the body in the pericardial cavity - the pericardium (the crustacean pericardium is not connected with the coelom, but is a section of the mixocoel). Blood enters the pericardium from the gills, sufficiently enriched with oxygen. The heart communicates with the pericardium by paired slit-like openings equipped with valves - ostia. Crayfish have 3 pairs of ostia, crayfish with a tubular heart can have many pairs. With the expansion (diastole) of the heart, blood enters it through the ostia from the pericardium. With the contraction (systole) of the heart, the valves of the ostia close and blood is driven from the heart through the arterial vessels to various parts of the body. Thus, the pericardial region of the mixocoel performs the function of the atrium.
In crayfish, the system of arterial vessels is quite strongly developed. Three vessels extend forward from the heart to the head and to the antennae. Back from the heart there is one vessel that carries blood to the abdomen, and two arteries that flow into the lower abdominal vessels. These vessels branch into smaller ones, and eventually the blood enters the sinuses of the mixocoel. Having given oxygen to the tissues and receiving carbon dioxide, the blood is collected in the abdominal venous sinus, from where it is sent through the afferent vessels to the gills, and from the gills through the efferent vessels to the pericardial region of the mixocel.
excretory system
The excretory organs of crustaceans are altered metanephridia. In crayfish and other higher crustaceans, the excretory organs are represented by one pair of glands located in the head part of the body and opening outward through holes at the base of the antennae. They are called antennal glands. The gland is a complexly twisted drip with glandular walls, consisting of three sections: white, transparent and green. At one end, the canal closes with a small coelomic sac, which is the remnant of the coelom. At the other end, the canal expands into the bladder and then opens with an opening to the outside. The excretory glands of crayfish are also called green glands due to their greenish color. Substances released from the blood diffuse into the walls of the channel, accumulate in the bladder and are released outside.
The rest of the crustaceans also have one pair of excretory glands of a similar structure, but they open outward not at the base of the antennae, but at the base of the second pair of maxillae. Therefore, they are called maxillary glands. In crustacean larvae developing with metamorphosis, the location of the excretory organs is reversed, namely: the larvae of higher crustaceans have maxillary glands, while the larvae of the rest have antennal glands. Apparently, this is due to the fact that the ancestors of crustaceans initially had two pairs of excretory organs - both antennal and maxillary. Subsequently, the evolution of crayfish followed different paths and led to the fact that in higher crustaceans only the antennal glands were preserved, and in the rest only the maxillary glands. Proof of the correctness of this point of view is the presence of two pairs of excretory glands in some crustaceans, namely in marine crayfish, from primitive higher crustaceans, and also in shellfish from lower crayfish.
Nervous system
The central nervous system of most crustaceans is represented by the ventral nerve cord and is very close to the nervous system of annelids. It consists of the supraesophageal ganglion (paired in origin), which forms the brain, connected with the subesophageal ganglion by peripharyngeal connectives. From the subesophageal ganglion comes a double ventral nerve trunk, forming a pair of contiguous ganglia in each segment.
In higher crustaceans, the nervous system reaches a relatively high level of development (the structure of the brain), while in other groups of crustaceans it has a more primitive character. An example of the most primitive structure is the nervous system of branchiopods, which have a head ganglion, near-pharyngeal connectives, and two relatively far-spaced nerve trunks extending from them. On the trunks in each segment there are small ganglionic thickenings, connected by double transverse commissures. In other words, the nervous system of these crayfish is built according to the ladder type.
In most crustaceans, there is a convergence of longitudinal nerve trunks, the paired ganglia of which merge together. In addition, as a result of the fusion of segments and the formation of body parts, their ganglia merge.
This process is associated primarily with the formation of the head (cephalization). So, the brain of crayfish (and other decapods) is formed by the head ganglion itself with two sections - the antennal and the antennal attached to it (the first pair of ganglia of the abdominal nerve chain that innervates the antennae). The subpharyngeal ganglion was formed by the fusion of the following 6 pairs of ganglia of the ventral nerve chain: ganglia innervating the mandibles, two pairs of maxillae, and three pairs of mandibles. This is followed by 11 pairs of ganglia of the abdominal chain - 5 thoracic and 6 abdominal.
On the other hand, fusion of ganglia may also take place due to the shortening of the body or small size in one or another group of crustaceans. Particularly interesting in this respect is the fusion of all the ganglia of the abdominal chain into one large knot observed in crabs.
sense organs
Crustaceans have organs of touch, organs of chemical sense (smell), organs of balance and organs of vision.
reproduction
With rare exceptions (barnacles), all crustaceans have separate sexes, and many have quite pronounced sexual dimorphism. Thus, the female crayfish differs in a noticeably wider abdomen and, as we know, in the structure of the first and second pairs of abdominal legs. In many lower crustaceans, males are significantly smaller than females.
Crustaceans reproduce exclusively sexually. In a number of groups of lower crustaceans (shieldmen, cladocerans, shellfish) parthenogenesis and alternation of parthenogenetic and bisexual generations take place.
Two subclasses - lower crustaceans (Entomostraca) and higher crustaceans (Malacostraca) - turned out to be untenable, since unrelated groups were combined in the subclass of lower crustaceans. The subclass of higher crustaceans has been preserved as a homogeneous group, descending from a single root.
The class of crustaceans (Crustacea) is divided into 4 subclasses: 1. Gills (Branchiopoda); 2. Jaws (Maxillopoda); 3. Shellfish (Ostracoda); 4. Higher crustaceans (Malacoslraca).
Subclass. Branchiopods (Branchiopoda)
The most primitive crustaceans. The head is free, does not grow together: with the chest. The thoracic legs are leaf-shaped, equipped with respiratory lobes (appendages), simultaneously perform the functions of movement, breathing and supplying food to the mouth. Abdominal limbs are absent in all, with the exception of shields. Nervous system of the ladder type. The subclass includes two major orders.
Order Gillfoot (Anostraca)
The cephalothoracic shield - carapace - is absent. Homonomously segmented body with a large number of segments (the branchiopod has 21 segments, not counting the head segments). The head consists of two sections - protocephalon (acron and antennal segment) and gnatocephalon (mandible segments, maxilla of the first and maxilla of the second).
The pectoral legs are arranged very primitively and have thin-walled outgrowths filled with hemolymph (blood) and performing a respiratory function. The circulatory system is represented by a long tubular heart with a pair of awns in each segment of the body. Nervous system of the ladder type. Branchiopods have paired compound eyes, but an unpaired naupliar ocellus has also been preserved. Development with metamorphosis (nauplius, metanauplius).
This order includes common freshwater crustaceans - branchiopods (Branchipus stagnalis). Gillnopods appear in large numbers in spring ponds. They are yellowish in color, with 11 pairs of thoracic legs and swim backwards. In salt lakes, crustaceans Artemia salina are common, capable of parthenogenetic reproduction (development). Among them, polyploid races were found, with an increase in the set of chromosomes by 3, 4, 5 and 8 times.
Order Leaf-legged (Phyllopoda)
There is a cephalothoracic shield, but it is different for different groups. The order includes three suborders.
Suborder 1. Shields (Notostraca). The largest animals among the branchiopods, more than 5-6 cm long. The body is covered with a wide flat cephalothoracic shield, which does not cover only 10-15 hind legless segments with a long furka, which ends with a telson. The number of body segments is variable (except for 5 head segments), it can reach 40 or more. On the front 12 segments (thoracic) there is one pair of leaf-shaped legs, and on the next several pairs (up to 5-6 pairs on one segment). A very primitive suborder, close in organization to the gilllegs. development with metamorphosis.
In stagnant spring ponds (often in large puddles) common shield bugs are found: Triops cancriformis, Lepidurus apus. Shields are interesting for their sporadic appearance in small ponds and rain puddles, often in large numbers. This is connected with the belief that shields supposedly fall from the sky with rain. In fact, everything is explained by the fact that wintering shield eggs can survive a long period outside the water and are carried by the wind.
The common shield (Triops cancriformis) is a real living fossil, this species has not changed its organization since the early Mesozoic (Triassic). Such constancy of the species for 200 million years can be explained by the very short period of its active life (3-4 weeks) and the extreme persistence of resting eggs.
Suborder 2. Conchostraca. Its representatives are ordinary benthic freshwater crustaceans, the body length of which is from 4 to 17 mm. Carapace in the form of a bivalve greenish-brown shell containing the entire body of the crustacean, with its numerous (from 10 to 32) leaf-shaped pectoral legs. These include large crustaceans Limnadia, Cyzicus, etc.
Suborder 3. Cladocera. In ponds, lakes and rivers, you can always find representatives of this suborder - small crustaceans, up to 2-3 mm (rarely 5 mm) in length, constituting a significant part of freshwater plankton, which often appear in huge numbers. Especially frequent are representatives of the Daphnia family, or water fleas: Daphnia magna, Daphnia pulex, Simocephalus vetulus, etc.
The gable, laterally flattened cephalothoracic shield - the carapace - of the cladocerans covers the entire body, but the head is not covered by it. The abdomen of Daphnia, bending, also hides under the shield. At the rear end, the shield often ends in a sharp spike. Daphnia has a beak-shaped head, in addition to the naupliar eye, also has an unpaired compound eye, consisting of a small number of ommatidia. The compound eye is driven by special muscles.
The antennae are very short, and the antennae are transformed into special locomotor organs, very strongly developed, biramous, and bearing pinnate setae. They are driven by strong muscles. When moving in the water, the cladocerans make strong waves with their antennae, and from each stroke their body bounces forward and upward. At the next moment, the antennae are brought forward for a new rowing movement, and the body of the crustacean descends somewhat. For these peculiar movements of daphnia, they received the name "water fleas."
There are 4-6 pairs of thoracic limbs in cladocerans, and in many, in particular, in Daphnia, they represent a kind of filtering apparatus. In these cladocerans, the limbs are shortened, equipped with feathery combs and make quick oscillatory movements. A constant flow of water is created, from which small algae, bacteria and detritus particles are filtered out. The filtered food is compressed and moved towards the mouth. With the help of this device, Daphnia filters out such an amount of food in 20-30 minutes that it can fill its entire intestine. In some predatory cladocerans, the pectoral legs are jointed and serve for grasping.
On the dorsal side of the body, closer to the head, the heart is located in the form of a small sac. It has one pair of awns and an outlet in the front. There are no blood vessels, and hemolymph circulates in the sinuses of the mixocoel. The nervous system is very primitive and is built, like in gill legs, according to the ladder type.
Of particular interest is the reproduction of cladocerans, in particular Daphnia. They have an alternation of several parthenogenetic and one bisexual generation. This type of reproduction is called heterogony.
The development of branched eggs takes place without metamorphosis (with the exception of one species). During the summer, only females are usually found, breeding parthenogenetically and laying "summer" eggs, which differ in that they have a double, diploid number of chromosomes.
Eggs are laid in a special brood chamber located under the shell on the dorsal side of the body, behind the heart.
The development is direct. The eggs hatch into young female daphnia.
With the deterioration of living conditions (lowering water temperature, reducing the food supply of the reservoir, which usually occurs in autumn), daphnia begin to lay eggs that have a haploid set of chromosomes. Of these, either only small males are formed (without fertilization), or the eggs need fertilization. The eggs of the last category are called resting. Males are 1.5-2.5 times smaller than the females they fertilize. Fertilized eggs differ from unfertilized ones in larger sizes and a greater amount of yolk. First, fertilized eggs (two eggs each) are placed in the brood chamber, and then a special saddle, the ephippium, is formed from a part of the daphnia shell. During molting, the ephippium separates from the shell of the mother and plays the role of a protective shell around the egg. Since gas bubbles form in the wall of the ephippium, it does not sink, and in autumn many ephippiums appear on the surface of the reservoir. Ephippiums are often equipped with spines, hooks on long threads, which ensures the spread of daphnia in fresh water. Floating on the surface of the water, ephippiums hook on to the feathers of waterfowl and can be carried by them to distant water bodies. Eggs enclosed in ephippiums overwinter and develop only in spring, when the first generation of females emerges from them.
In various cladocerans, a change in body shape is observed depending on living conditions. Often these changes are of a regular seasonal nature, which is associated with periodic seasonal changes in conditions, and are called cyclomorphosis.
Cladocerans play an important role in the nutrition of freshwater fish, especially fry. Therefore, fish farmers are extremely interested in enriching the cladoceran fauna. Methods for artificial breeding of daphnia and enrichment of reservoirs with them have been developed.
Subclass. Jaw-footed (Maxillopoda)
Marine and freshwater crustaceans. The number of thoracic segments is constant (usually 6, in some species 5 or 4). The thoracic legs have a motor or water-motor function, they do not participate in respiration. There are no ventral legs.
Small crustaceans, 1-2 mm, rarely 10 mm long, without cephalothoracic shield. The order includes about 2000 species. Most copepods are planktonic forms. Spreading their long antennules to the sides, they really hover on them in the water column. In addition to hovering in plankton and galloping (Cyclops) forms, there are also benthic forms among the copepods. In fresh waters, representatives of the genera Cyclops and Diaptomus are common.
Copepods are characterized by the following structural features. The antennae are strongly developed and play the role of oars in the cyclops or a soaring apparatus in other copepods. Adaptations for “floating” in water are sometimes sharply pronounced: the antennules and pectoral limbs of some marine copepods are seated with long feathery bristles directed to the sides, which greatly increases the surface of their body.
In males, the antennules are often converted into female holding organs during mating. The other head limbs function largely like swimming legs.
The thoracic limbs are primitive, have a typical biramous character, but do not bear gills. They are important locomotor organs. They are responsible for the spasmodic movements of copepods.
The cephalothorax is formed by five fused head segments and one pectoral. There are usually 4 free thoracic segments, and 3-5 abdominal segments, with a furca at the end. There are no gills, breathing takes place on the entire surface of the body. In this regard, the heart in most forms is absent.
There is only an unpaired naupliar eye. Hence the name Cyclopes (Cyclops are the one-eyed giants of Greek mythology).
The biology of reproduction of copepods is interesting. Sexual dimorphism is common, expressed mainly in the smaller size of males and in the structure of their antennules. After mating, females lay eggs that stick together with a special secret and form one or two egg sacs, which remain attached to the genital openings of the females until the larvae emerge from them.
A nauplius larva emerges from the egg, turning after molting into a metanauplius, which molts three more times, and as a result a third, copepoid larva is obtained, after several molts turning into an adult form.
Among crustaceans, copepods occupy a special place in terms of their great importance for the nutrition of many animals, primarily fish and whales. If cladocerans make up a very significant part of freshwater plankton, then copepods are the most important part of marine plankton, and many of them are also common in fresh waters. Marine plankton is characterized by representatives of the genus Calanus and others, which often appear, especially in the northern seas, in large numbers, causing a change in the color of the water.
Order Barnacles (Cirripedia)
Sea acorns (Balanus) often cover underwater objects in large numbers: stones, piles, mollusk shells. From the outside, a calcareous shell of a truncated-conical shape is visible, formed by separate plates fused together. With a wider base, the shell adheres to the substrate, and on the opposite side there is a calcareous cap made of movable plates. The lid of the live balancer opens, and a bundle of segmented, mustache-shaped, biramous pectoral legs protrudes from it, which are in constant rhythmic movement, which ensures both the supply of food to the mouth and breathing. This is the only external sign indicating that we have an arthropod in front of us.
Sea ducks (Lepas) differ from sea acorns in shape and in that the lower (head) section forms a special stalk not covered with a shell - a leg. The animal is placed inside the shell on the dorsal side, feet up. Folds of skin - the mantle - adjoin the walls of the shell.
At young stages of development, barnacles attach to the substrate with their head end, and antennules and special cement glands take part in this.
The belonging of barnacles to crustaceans is proved by the fact that a typical nauplius comes out of their eggs, which then turns into a metanauplius. The latter turns into a cypris-shaped larva typical of barnacles, with a bivalve shell. It is called so because it is similar to the Cypris barnacle. This larva is attached to the substrate with the help of aptennula and turns into a sessile form of barnacle.
Barnacles are hermaphrodites, but some species have small additional males. Fertilization is usually cross. The development of hermaphroditism in barnacles is associated with their transition to a sedentary lifestyle.
Subclass Shell (Ostracoda)
These are very small crustaceans, most often 1-2 mm in size, found in large numbers in marine and fresh waters, mainly bottom creeping forms, although among marine species there are also floating - planktonic. The number of genera and species is large: about 1500 species of shellfish are known in the seas and fresh waters.
A characteristic feature of shellfish is a bivalve cephalothoracic shield, resembling a shell and completely hiding the entire body of the animal, in contrast to cladocerans, which have a free head.
The organization of shellfish is very simplified. Many have no circulatory system and gills, while others have only a heart. The body of the shellfish is greatly shortened. The head bears five pairs of appendages, while the thorax bears only 1-2 pairs. Abdominal legs are absent, and in some forms the abdomen is equipped with a furka. For most, only parthenogenetic females are known.
Shellfish move quickly and smoothly in the water, and the antennules and antennas serve as swimming organs. Cypris can also crawl on the substrate using its antennae and pectoral legs.
A common representative - Cypris - is found in almost any fresh water body; the crustacean Cypridina is also common in the seas.
Subclass Higher crustaceans (Malacoslraca)
The most highly organized of the crustaceans, at the same time retaining some primitive structural features. The number of body segments is definite: four head (not counting the acron), eight chest and six (or seven in thin-shelled) abdominal, not counting the telson. The abdominal segments have limbs (6 pairs). There are no forks, or furks, except for thin-shelled crayfish. Segmentation is more heteronomous compared to representatives of other subclasses. In many forms, a cephalothorax is formed by attaching 1-2-3 thoracic segments to the head segments. In some forms, the primitive primary head, the protocephalon, remains isolated. The circulatory system is developed, in addition to the heart there are always blood vessels. The respiratory system in most species is represented by gills associated with the thoracic or abdominal limbs.
The excretory organs of adult cancers are the antennal glands. Only thin-shelled ones also have maxillary glands at the same time.
Development with metamorphosis or direct. During development with metamorphosis, the nauplius stage passes, with rare exceptions, in the egg shells. The egg usually hatches into a zoea or mysid stage larva. The subclass includes several units.
Detachment Thin-shelled, or Nebalia (Leptostraca)
Nebalii are a very small group of small crustaceans (only 6 species are known). They are interesting in that they have signs of the most primitive organization among higher crayfish and show similarities with branchiopods. The presence of ventral limbs and antennal glands brings Nebalia closer to higher crustaceans. However, unlike all other higher cancers, they have not 6, but 7 segments of the abdomen, the anal segment of the abdomen ends with a fork. Other signs are also characteristic of nebalia: 1) a gable shell covering the chest and part of the abdomen; 2) eight pairs of identical biramous limbs, similar to the legs of branchiopods; 3) the presence in adults of two pairs of excretory glands at the same time - antennal and rudimentary maxillary.
The Nebalii are a very ancient group, and seem to be closest to the extinct, ancestral primordial crustaceans that were the ancestors of all modern crustacean subclasses.
Order Mysididae (Mysidacea)
Mysids are a peculiar group of predominantly marine crayfish, outwardly similar to small shrimp. It includes about 500 species leading a near-bottom or planktonic lifestyle. Body sizes from 1-2 to 20 cm in bottom deep-sea forms.
Mysids have stalked eyes. The body of mysids is equipped with a carapace covering only 8 pairs of pectoral biramous swimming legs. Abdomen with poorly developed limbs, long and free. Females have a brood chamber formed by processes of the pectoral legs. The development is direct.
Interesting is the ability of mysids to endure significant desalination, which gives them the opportunity to penetrate from the seas into rivers and fresh lakes.
In Russia, mysids are common in the Caspian Sea and in desalinated areas of the Black and Azov Seas. They come upstream of large rivers and their tributaries, populate the newly created reservoirs on them. Some types of mysids are found only in fresh waters. Mysids are of rather great practical importance, as they serve as food for many commercial fish.
Order Equinopods (Isopoda)
The body of isopods is flattened dorsoventrally. The cephalothorax consists of head segments fused together, to which one or two thoracic segments have joined. The cephalothorax is movably articulated with the rest of the thoracic segments. The carapace is missing. Thoracic limbs are single-branched, walking type; abdominal limbs are lamellar, performing the function of gills. In connection with the position of the gills on the abdomen, the tubular heart is also located in the last two thoracic segments and in the abdomen. The system of arterial blood vessels is developed.
In woodlice, in connection with the terrestrial way of life, adaptations arise for breathing atmospheric air. The common woodlice - it is not for nothing that it is called so - can only live in a humid environment; in sufficiently dry air, many woodlice quickly die. The edges of the dorsal scutes of woodlice descend low along the sides of the body and are pressed against the substrate on which it sits. This maintains sufficient moisture on the ventral side of the body, where the modified gills are placed. Another species of woodlice, the coagulating woodlouse (Armadillidium cinereum), can live in drier areas.
Many woodlice breathe with gills, which are protected from drying out by a kind of gill cover (a modified pair of gill legs). The gills are moistened with drip water caught by the sculpture of the integument or the hind abdominal legs - uropods. Some of the woodlice are able to excrete fluid through the anus, which helps to maintain a film of water covering the gills.
Finally, many woodlice develop so-called pseudotracheae. An invagination is formed on the anterior abdominal legs, leading to a cavity from which thin branching tubes filled with air extend. Unlike real trachea, chitin does not form a spiral thickening in them.
Many species of woodlice live in the soil, where they can harm crop plants. .Some of them live in deserts, where they are very numerous and can be beneficial by participating in the cycle of organic matter and soil-forming processes. Desert species of woodlice from the genus Hemilepistus live in Central Asia, sometimes found in very large numbers.
Order Amphipoda (Amphipoda)
In terms of the level of organization, amphipods are close to isopods. In amphipods, the cephalothorax is also formed by a fused head and one thoracic segment. They also do not have a cephalothoracic shield and their thoracic limbs are single-branched. But at the same time, amphipods are quite different from isopods. Their body is not flattened in the dorsoventral, but in the lateral direction and curved to the ventral side. The gills are placed on the thoracic legs. Females have special plates on 2-5 pairs of thoracic legs, which together form a brood chamber. In connection with the position of the gills on the thoracic limbs, the tubular heart is also placed in the thoracic region. Three pairs of anterior ventral biramous limbs serve for swimming. The posterior three pairs of ventral legs are jumping. Therefore, the order of amphipods has the Latin name Amphipoda, which means diversified.
Among marine amphipods, many lead a coastal lifestyle and even live in algae thrown by the surf, in holes dug in the sand. Such, for example, are sand racers (Talitrus saltator). In fresh waters, the amphipod flea (Gammarus pulex) is common, living in shallow places in rivers and lakes.
A large number of unique amphipod species found nowhere else (about 240) live in Lake Baikal. Amphipods are important in the diet of various fish.
Order Decapods (Decapoda)
The decapod crayfish order unites about 8500 species of the most highly organized crustaceans, often reaching very large sizes. Many of them are edible. Far Eastern king crab, crayfish, some other crabs, shrimp are the subject of fishing. Features of the organization of decapod crayfish are known from the general characteristics of the class of crustaceans.
All decapods have stalked eyes, the first three thoracic segments are part of the cephalothorax, the cephalothoracic shield - the carapace - grows together with all the thoracic segments, and does not cover them, like in other crustaceans.
Most decapods are marine animals, but some live in fresh waters. Species leading a benthic, demersal lifestyle (crayfish, crabs, hermit crabs, etc.) predominate. Very few (some crabs) have adapted to life on land. Various types of crayfish live in fresh waters, and river crab is found in the mountain rivers of the Crimea and the Caucasus.
The decapod crayfish order is divided into three suborders: long-tailed crayfish (Macrura), soft-tailed crayfish (Anomura) and short-tailed crayfish (Brachiura).
Long-tailed crayfish have a long abdomen with well-developed abdominal legs. Long-tailed crayfish, in turn, can be divided into crawling and swimming.
The former are primarily crayfish. Two of the most widespread commercial species of crayfish live in Russia: broad-toed (Astacus astacus) and narrow-toed (A. leptodactylus). You meet first; in the basin of rivers flowing into the Baltic Sea, the second - in the rivers flowing into the Black, Azov, Caspian Seas, in the Azov and Caspian Seas and in the reservoirs of Western Siberia. Usually these species do not occur together. When living together, the narrow-toed crayfish displaces the more valuable broad-toed crayfish. Of the sea crawling long-tailed crayfish, the most valuable are large lobsters, the length of which can exceed 80 cm, and spiny lobsters (up to 75 cm), common in the Mediterranean Sea and in different parts of the Atlantic Ocean.
Floating long-tailed crayfish are represented in the seas by many species of shrimp. Unlike bottom crustaceans - crayfish, lobster, etc., in which the body is rather wide, the body of shrimp is flattened from the sides, which is explained by the floating lifestyle.
Shrimps are eaten, especially by the population of coastal cities. In some countries they serve as a subject of fishing.
Soft-tailed crayfish are usually benthic forms living at various depths. Characteristic features of soft-tailed crayfish are a softer abdomen covered with less hard covers, a very often observed asymmetry of claws and abdomen, and underdevelopment of some abdominal limbs.
This suborder includes a biologically interesting group of hermit crabs. They stick their soft belly into suitable-sized empty gastropod shells and drag them along. When danger approaches, the hermit crab hides completely in the shell, covering the mouth with a more developed claw. Growing up, the hermit crab changes its shell to a larger one. Hermit crabs often have a curious symbiosis with sea anemones. Some anemones settle on a shell occupied by a hermit crab. This gives anemones "mobility", and hermit crabs are better protected, having on the shell armed with stinging cells and almost inedible anemones. Also curious is the symbiosis of hermit crabs with sponges settling on their shells.
Soft-tailed crayfish also include some species that have an external resemblance to real crabs (a wide and short cephalothorax and a largely reduced abdomen). This is primarily a large commercial king crab (Paralithodes camtschatica), reaching 1.5 m in the span of the limbs. He lives in the Far Eastern seas (Japanese, Okhotsk and Bering).
Finally, a very interesting robber crab, or palm thief, reaching a length of 30 cm, belongs to the soft-tailed crayfish. It lives on the islands of the Pacific Ocean and is interesting as a form adapted to life on land. It hides in burrows lined with fibers from coconuts. Instead of gills, he has only their rudiments, and the gill cavities on the sides of the cephalothoracic shield are turned into peculiar lungs. The palm thief feeds mainly on the falling fruit of various palms, which it smashes with its strong claws, and preys on weakened animals.
Short-tailed crayfish have a small, always bent abdomen. These include real crabs.
Crabs are typical benthic animals, well adapted to life among stones, rocks, coral reefs in the surf zone of the sea, but there are forms that live at great depths. The Far Eastern seas are especially rich in crabs. In the Black Sea, stone crab (Cancer pagurus) is not very large, with strong claws, as well as other, smaller species.
The largest representative of crustaceans, living at great depths in the Far Eastern seas, also belongs to crabs, the giant Japanese crab (Macrocheria kaempferi), reaching 3 m between the ends of the elongated middle pectoral legs.
Phylogeny of crustaceans
In the study of crustaceans, we became acquainted with many facts indicating the possibility of their origin from annelids. The most important of these facts are: 1) the parapodial type of structure of the most primitive biramous limbs; 2) the nature of the structure of the nervous system - the ventral nerve chain or the more primitive ladder nervous system of the branchiopods; 3) the type of structure of the excretory organs derived from the metanephridia of polychaetes; 4) the tubular heart in the most primitive crustaceans, resembling the dorsal blood vessel of annelids.
Various groups of crustaceans are already known to us from Paleozoic deposits, which indicates a very great antiquity of their origin.
The most primitive group among modern crustaceans is undoubtedly the subclass of branchiopods. Signs of branchiopods that are especially important in this respect are: 1) an indefinite and often large number of body segments; 2) homonomy of segmentation of their body; 3) the primitive structure of the thoracic limbs; 4) ladder type of structure of the nervous system. There is no doubt closeness in origin between branchiopods and cladocerans, the latter being, however, a much more specialized group (antennae, brood chamber, alternation of generations).
Copepods, while possessing some primitive features, are otherwise more progressive. Thus, they have a head formed by five completely fused segments, and the total number of body segments is always definite and reduced to 14. The absence of some organs in copepods, such as compound eyes and heart, should be considered as the result of secondary reduction.
The higher crustaceans undoubtedly have a more perfect organization than all other groups of crustaceans. However, they are not related to any of the groups of low-organized crayfish, as they retained some very primitive features, such as the presence of abdominal limbs, which were completely reduced in other groups. The primary head - protocephalon - is also characteristic of many orders of higher crayfish, while in other subclasses it is less common.
Subclass Gillpods
The most primitive These small crustaceans have leaf-shaped legs and are used equally for locomotion and respiration. They also create a current of water that brings food particles to the mouth. Their eggs easily tolerate desiccation and wait in the soil for the new rainy season. Artemia is interesting among the branchiopods: it can live in salt lakes with a salt concentration of up to 300 g / l, and dies in fresh water after 2-3 days.
