Star fish

Starfish or sea stars are echinoderms belonging to the class Asteroidea. The names "starfish" and "sea star" essentially refer to members of the Class Asteroidea. However, common usage frequently finds "starfish" and "sea star" also applied to ophiuroids which are correctly referred to as "brittle stars" or "basket stars".

There are 2,000 living species of starfish that occur in all the world's oceans, including the Atlantic, Pacific, Indian as well as in the Arctic and the Southern Ocean (i.e., Antarctic) regions. Starfish occur across a broad depth range from the intertidal to abyssal depths (>6000 m).

Starfish are among the most familiar of marine animals and possess a number of widely known traits, such as regeneration and feeding on mussels. Starfish possess a wide diversity of body forms and feeding methods. The extent that Asteroidea can regenerate varies with individual species. Broadly speaking, starfish are opportunistic feeders, with several species having specialized feeding behavior, including suspension feeding and specialized predation on specific prey.

The Asteroidea occupy several important roles throughout ecology and biology. Sea stars, such as the Ochre sea star (Pisaster ochraceus) have become widely known as the example of the keystone species concept in ecology. The tropical Crown of Thorns starfish (Acanthaster planci) are voracious predators of coral throughout the Indo-Pacific region. Other starfish, such as members of the Asterinidae are frequently used in developmental biology.

Appearance

Starfish express pentamerism or pentaradial symmetry as adults. However, the evolutionary ancestors of echinoderms are believed to have had bilateral symmetry. Starfish, as well as other echinoderms, do exhibit bilateral symmetry, but only as larval forms. Most starfish typically have five rays or arms, which radiate from a central disk. However, several species frequently have six or more arms. Several asteroid groups, such as the Solasteridae, have 10-15 arms whereas some species, such as the Antarctic Labidiaster annulatus can have up to 50. It is not unusual for species that typically have five-rays to exceptionally possess five or more rays due to developmental abnormalities. The bodies of starfish are composed of calcium carbonate components, known as ossicles. These form the endoskeleton, which takes on a variety of forms that are externally expressed as a variety of structures, such as spines and granules. The architecture and individual shape/form of these plates which often occur in specific patterns or series, as well as their location are the source of morphological data used to classify the different groups within the Asteroidea. Terminology referring to body location in sea stars is usually based in reference to the mouth to avoid incorrect assumptions of homology with the dorsal and ventral surfaces in other bilateral animals. The bottom surface is often referred to as the oral or actinal surface whereas the top surface is referred to as the aboral or abactinal side. The body surface of sea stars often has several structures that comprise the basic anatomy of the animal and can sometimes assist in its identification. The madreporite can be easily identified as the light-colored circle, located slightly off center on the central disk. This is a porous plate which is connected via a calcified channel to the animal's water vascular system in the disk. Its function is, at least in part, to provide additional water for the animal's needs, including replenishing water to the water vascular system. Several groups of asteroids, including the Valvatacea but especially the Forcipulatacea possess small bear-trap or valve-like structures known as pedicellariae. These can occur widely over the body surface. In forcipulate asteroids, such as Asterias or Pisaster, pedicellariae occur in pom-pom like tufts at the base of each spine, whereas in goniasterids, such as Hippasteria, pedicellariae are scattered over the body surface. Although the full range of function for these structures is unknown, some are thought to act to act as defense where others have been observed to aid in feeding. The Antarctic Labidiaster annulatus uses its large, pedicellariae to capture active krill prey. The North Pacific Stylasterias has been observed to capture small fish with its pedicellariae. Other types of structures vary by taxon. For example, Porcellanasteridae employ additional cribriform organs which occur among their lateral plate series, which are thought to generate current in the burrows made by these infaunal sea star.

Internal anatomy

As echinoderms, starfish possess a hydraulic water vascular system that aids in locomotion. The water vascular system has many projections called tube feet on the ventral face of the sea star's arms which function in locomotion and aid with feeding. Tube feet emerge through openings in the endoskeleton and are externally expressed through the open grooves present along the bottom of each arm. The body cavity not only contains the water vascular system that operates the tube feet, but also the circulatory system, called the hemal system. Hemal channels form rings around the mouth (the oral hemal ring), closer to the top of the sea star and around the digestive system (the gastric hemal ring). A portion of the body cavity called the axial sinus connects the three rings. Each ray also has hemal channels running next to the gonads. On the end of each arm or ray there is a microscopic eye (ocellus), which allows the sea star to see, although it only allows it to see light and dark, which is useful to see movement. Only part of the cells are pigmented (thus a red or black color) and there is no cornea or iris. This eye is known as a pigment spot ocellus. Several types of toxins and secondary metabolites have been extracted from several species of sea star. Research into the efficacy of these compounds for possible pharmacological or industrial use occurs worldwide.

Digestive system

The mouth of a starfish is located on the underside of the body, and opens through a short esophagus into firstly a cardiac stomach, and then, a second, pyloric stomach. Each arm also contains two pyloric caeca, long hollow tubes branching outwards from the pyloric stomach. Each pyloric caecum is lined by a series of digestive glands, which secrete digestive enzymes and absorb nutrients from the food. A short intestine runs from the upper surface of the pyloric stomach to open at an anus in the center of the upper body.

Many sea stars, such as Astropecten and Luidia swallow their prey whole, and start to digest it in the stomachs before passing it into the pyloric caeca. However, in a great many species, the cardiac stomach can be everted out of the organism's body to engulf and digest food. In these species, the cardiac stomach fetches the prey then passes it to the pyloric stomach, which always remains internal.

Some species are able to use their water vascular systems to force open the shells of bivalve mollusks such as clams and mussels by injecting their stomachs into the shells. With the stomach inserted inside the shell, the sea star is able to digest the mollusk in place. The cardiac stomach is then brought back inside the body, and the partially digested food is moved to the pyloric stomach. Further digestion occurs in the intestine. Waste is excreted through the anus on the aboral side of the body.

Because of this ability to digest food outside of its body, the sea star is able to hunt prey that are much larger than its mouth would otherwise allow, such as clams and oysters, arthropods, small fish, and mollusks. However, some species are not pure carnivores, and may supplement their diet with algae or organic detritus. Some of these species are grazers, but others trap food particles from the water in sticky mucus strands that can be swept towards the mouth along ciliated grooves.

Some echinoderms can live for several weeks without food under artificial conditions. Scientists believe that they may receive some nutrients from organic material dissolved in seawater.

Nervous system

Echinoderms have rather complex nervous systems, but lack a true centralized brain. All echinoderms have a network of interlacing nerves called a nerve plexus which lies within, as well as below, the skin. The esophagus is also surrounded by a central nerve ring which sends radial nerves into each of the arms, often parallel with the branches of the water vascular system. The ring nerves and radial nerves coordinate the sea star's balance and directional systems.
Although the echinoderms do not have many well-defined sensory inputs, they are sensitive to touch, light, temperature, orientation, and the status of water around them. The tube feet, spines, and pedicellariae found on sea stars are sensitive to touch, while eyespots on the ends of the rays are light-sensitive. The tube feet, especially those at the tips of the rays, are also sensitive to chemicals and this sensitivity is used in locating odor sources, such as food.
The eyespots each consist of a mass of ocelli, consisting of pigmented epithelial cells that respond to light and narrow sensory cells lying between them. Each ocellus is covered by a thick, transparent, cuticle that both protects them and acts as a lens. Many starfish also possess individual photoreceptor cells across their body and are able to respond to light even when their eyespots are covered.

Source:http://en.wikipedia.org/wiki/Starfish

Shark

Sharks (superorder Selachimorpha) are a type of fish with a full cartilaginous skeleton and a highly streamlined body. The earliest known sharks date from more than 420 million years ago, before the time of the dinosaurs. Since that time, sharks have diversified into 440 species, ranging in size from the small dwarf lanternshark, Etmopterus perryi, a deep sea species of only 17 centimetres (6.7 in) in length, to the whale shark, Rhincodon typus, the largest fish, which reaches approximately 12 metres (39 ft 4 in) and which feeds only on plankton, squid, and small fish through filter feeding. Sharks are found in all seas and are common down to depths of 2,000 metres (6,562 ft). They generally do not live in freshwater, with a few exceptions such as the bull shark and the river shark which can live both in seawater and freshwater. They respire with the use of five to seven gill slits. Sharks have a covering of dermal denticles that protect their skin from damage and parasites and improve fluid dynamics so the shark can move faster. They have several sets of replaceable teeth. Well-known species such as the great white shark, tiger shark, and the hammerhead are apex predators, at the top of the underwater food chain. Their extraordinary skills as predators fascinate and frighten humans, even as their survival is under serious threat from fishing and other human activities.

Physical characteristics:

Shark skeletons are very different from those of bony fish and terrestrial vertebrates. Sharks and other cartilaginous fish (skates and rays) have skeletons made of cartilage and connective tissue. Cartilage is flexible and durable, yet has about half the density of bone. This reduces the skeleton’s weight, saving energy. Sharks have no rib cage and therefore on land a shark's own weight can literally crush it.

Jaw

Like its relatives, rays and skates, the shark's jaw is not attached to the cranium. The jaw's surface, like the shark's vertebrae and gill arches, needs extra support due to its heavier exposure to physical stress and its need for strength. It has a layer of tiny hexagonal plates called "tesserae", which are crystal blocks of calcium salts arranged as a mosaic. This gives these areas much of the same strength found in the real bony tissue found in other animals. Generally there is only one layer of tesserae in sharks, but the jaws of large specimens, such as the bull shark, tiger shark, and the great white shark, have two to three layers or more, depending on body size. The jaws of a large white shark may have up to five layers. In the rostrum (snout), the cartilage can be spongy and flexible to absorb the power of impacts.

Teeth

Main article: Shark teeth The teeth of sharks are embedded in the gums rather than directly fixed to the jaw, and are constantly replaced throughout the shark's life. Multiple rows of replacement teeth are grown in a groove on the inside of the jaw and moved forward in a "conveyor belt"; some sharks lose 30,000 or more teeth in their lifetime. The rate of tooth replacement varies from once every 8–10 days to several months. In most species teeth are replaced one at a time, while in the cookiecutter sharks the entire row of teeth is replaced simultaneously. The shape of a shark's tooth depends on its diet: those that feed on mollusks and crustaceans have dense flattened teeth for crushing, those that feed on fish have needle-like teeth for gripping, and those that feed on larger prey such as mammals have pointed lower teeth for gripping and triangular upper teeth with serrated edges for cutting. The teeth of plankton-feeders such as the basking shark are greatly reduced and non-functional.

Fins

The fin skeletons are elongated and supported with soft and unsegmented rays named ceratotrichia, filaments of elastic protein resembling the horny keratin in hair and feathers. Sharks can only drift away from objects directly in front of them because their fins do not allow them to swim backwards.

Dermal denticles

Main article: Dermal denticle Unlike bony fish, sharks have a complex dermal corset made of flexible collagenous fibers and arranged as a helical network surrounding their body. This works as an outer skeleton, providing attachment for their swimming muscles and thus saving energy. In the past, sharkskin has been used as sandpaper. Their dermal teeth give them hydrodynamic advantages as they reduce turbulence when swimming.

Tails

Sharks have very distinctive tails. The tails (caudal fins) of sharks vary considerably between species and are adapted to the lifestyle of the shark. The tail provides thrust and so speed and acceleration are dependent on tail shape. Different tail shapes have evolved in sharks adapted for different environments. Sharks possess a heterocercal caudal fin in which the dorsal portion is usually noticeably larger than the ventral portion. This is due to the fact that the shark's vertebral column extends into that dorsal portion, allowing for a greater surface area for muscle attachment which would then be used for more efficient locomotion among the negatively buoyant cartilaginous fishes. This is in contrast to most bony fishes, which possess a homocercal caudal fin.

The tiger shark's tail has a large upper lobe which delivers the maximum amount of power for slow cruising or sudden bursts of speed. The tiger shark must be able to twist and turn in the water easily when hunting to support its varied diet, whereas the porbeagle, which hunts schooling fish such as mackerel and herring has a large lower lobe to help it keep pace with its fast-swimming prey. Some tail adaptations have other purposes. The thresher feeds on fish and squid, which it herds and stuns with its

Physiology

Buoyancy

Unlike bony fish, sharks do not have gas-filled swim bladders for buoyancy. Instead, sharks rely on a large liver, filled with oil that contains squalene and the fact that cartilage is about half as dense as bone. The liver constitutes up to 30% of their body mass. The liver's effectiveness is limited, so sharks employ dynamic lift to maintain depth and then sink when they stop swimming. Sand tiger sharks are also known to store air in their stomachs, using the stomach as a swim bladder. Most sharks need to constantly swim in order to breathe and cannot sleep very long, if at all, or they will sink. However certain shark species, like the nurse shark, are capable of pumping water across their gills, allowing them to rest on the ocean bottom.

Some sharks, if inverted or stroked on the nose, enter a natural state of tonic immobility. Researchers can use this condition to handle sharks safely.

Respiration

Like other fish, sharks extract oxygen from seawater as it passes over their gills. Unlike other fish, shark gill slits are not covered, but lie in a row behind the head. A modified slit called a spiracle lies just behind the eye; the spiracle assists water intake during respiration and plays a major role in bottom dwelling sharks. Spiracles are reduced or missing in active pelagic sharks. While the shark is moving, water passes through the mouth and over the gills in a process known as "ram ventilation". While at rest, most sharks pump water over their gills to ensure a constant supply of oxygenated water. A small number of species have lost the ability to pump water through their gills and must swim without rest. These species are obligate ram ventilators and would presumably asphyxiate if unable to move. Obligate ram ventilation is also true of some pelagic bony fish species.

The respiration and circulation process begins when deoxygenated blood travels to the shark's two-chambered heart. Here the shark pumps blood to its gills via the ventral aorta artery where it branches off into afferent brachial arteries. Reoxygenation takes place in the gills and the reoxygenated blood flows into the efferent brachial arteries, which come together to form the dorsal aorta. The blood flows from the dorsal aorta throughout the body. The deoxygenated blood from the body then flows through the posterior cardinal veins and enters the posterior cardinal sinuses. From there blood enters the heart ventricle and the cycle repeats.

Thermoregulation

Most sharks are "cold-blooded", or more precisely poikilothermic, meaning that their internal body temperature matches that of their ambient environment. Members of the family Lamnidae, such as the shortfin mako shark and the great white shark, are homeothermic and maintain a higher body temperature than the surrounding water. In these sharks, a strip of aerobic red muscle located near the center of the body generates the heat, which the body retains via a countercurrent exchange mechanism by a system of blood vessels called the rete mirabile ("miraculous net"). The common thresher shark has a similar mechanism for maintaining an elevated body temperature, which is thought to have evolved independently.

Osmoregulation

In contrast to bony fish, with the exception of the Coelacanth, the blood and other tissue of sharks and Chondrichthyes in general is isotonic to their marine environments because of the high concentration of urea and trimethylamine N-oxide (TMAO), allowing them to be in osmotic balance with the seawater. This adaptation prevents most sharks from surviving in fresh water, and they are therefore confined to marine environments. A few exceptions to this rule exist, such as the bull shark which has developed a way to change its kidney function to excrete large amounts of urea. When a shark dies the urea is broken down to ammonia by bacteria — because of this, the dead body will gradually start to smell strongly of ammonia.

Senses

Smell

Sharks have keen olfactory senses, located in the short duct (which is not fused, unlike bony fish) between the anterior and posterior nasal openings, with some species able to detect as little as one part per million of blood in seawater. They are more attracted to the chemicals found in the guts of many species, and as a result often linger near or in sewage outfalls. Some species, such as nurse sharks, have external barbels that greatly increase their ability to sense prey.

Sight

Shark eyes are similar to the eyes of other vertebrates, including similar lenses, corneas and retinas, though their eyesight is well adapted to the marine environment with the help of a tissue called tapetum lucidum. This means that sharks can contract and dilate their pupils, like humans, something no teleost fish can do. This tissue is behind the retina and reflects light back to it, thereby increasing visibility in the dark waters. The effectiveness of the tissue varies, with some sharks having stronger nocturnal adaptations. Sharks have eyelids, but they do not blink because the surrounding water cleans their eyes. To protect their eyes some species have nictitating membranes. This membrane covers the eyes during predation, and when the shark is being attacked. However, some species, including the great white shark (Carcharodon carcharias), do not have this membrane, but instead roll their eyes backwards to protect them when striking prey. The importance of sight in shark hunting behavior is debated. Some believe that electro- and chemoreception are more significant, while others point to the nictating membrane as evidence that sight is important. Presumably, the shark would not protect its eyes were they unimportant. The use of sight probably varies with species and water conditions. In effect the shark's field of vision can swap between monocular and stereoscopic at any time.

Hearing

Although it is hard to test sharks' hearing, they may have a sharp sense of hearing and can possibly hear prey many miles away. A small opening on each side of their heads (not to be confused with the spiracle) leads directly into the inner ear through a thin channel. The lateral line shows a similar arrangement, which is open to the environment via a series of openings called lateral line pores. This is a reminder of the common origin of these two vibration- and sound-detecting organs that are grouped together as the acoustico-lateralis system. In bony fish and tetrapods the external opening into the inner ear has been lost.

Source:http://en.wikipedia.org/wiki/Shark