Latimeria is a rare genus of fish which contains the two only living species of coelacanth. It includes two extant species: the West Indian Ocean coelacanth (Latimeria chalumnae) and the Indonesian coelacanth (Latimeria menadoensis). They follow the oldest known living lineage of Sarcopterygii (lobe-finned fish and tetrapods), which means they are more closely related to lungfish and tetrapods (amphibians, reptiles and mammals) than to the common ray-finned fishes and cartilaginous fishes. They are found along the coastlines of the Indian Ocean and Indonesia. Since there are only two known species of coelacanth and both are threatened, it is one of the most endangered genera of animals in the world. The West Indian Ocean coelacanth is a critically endangered species.
Description
Coelacanths of genus Latimeria are large, plump, lobe-finned fish that can grow to more than 2 m (6.6 ft) and weigh around 90 kg (200 lb). They are estimated to live up to 100 years, based on analysis of annual growth marks on scales, and reach maturity around the age of 55; the oldest known specimen was 84 years old at the time of its capture in 1960. Based on growth rings in the creatures' ear bones (otoliths), scientists infer that individual coelacanths may live as long as 80 to 100 years. Coelacanths live as deep as 700 m (2300 ft) below sea level, but are more commonly found at depths of 90 to 200 m (300 to 660 ft). Living examples of Latimeria chalumnae have a deep blue color which probably camouflages them from prey species; meanwhile, the Indonesian species (L. menadoensis) is brown.
Anatomy and physiology Coelacanth eyes are very sensitive, and have a tapetum lucidum. Coelacanths are almost never caught in the daytime, but have been caught at all phases of the moon. Coelacanth eyes have many rods, receptors in the retina that help animals see in dim light. Together, the rods and tapetum help the fish see better in dark water. The eye is acclimatized to seeing in poor light by rods that absorb mostly short wavelengths. Coelacanth vision has evolved to a mainly blue-shifted color capacity. Pseudomaxillary folds surround the mouth and replace the maxilla, a structure absent in coelacanths. Two nostrils, along with four other external openings, appear between the premaxilla and lateral rostral bones. The nasal sacs resemble those of many other fish and do not contain an internal nostril. The coelacanth's rostral organ, contained within the ethmoid region of the braincase, has three unguarded openings into the environment and is used as a part of the coelacanth's laterosensory system. The coelacanth's auditory reception is mediated by its inner ear, which is very similar to that of tetrapods and is classified as being a basilar papilla. The coelacanth's heart is shaped differently from that of most modern fish, with its chambers arranged in a straight tube. The coelacanth's braincase is 98.5% filled with fat; only 1.5% of the braincase contains brain tissue. The cheeks of the coelacanth are unique because the opercular bone is very small and holds a large soft-tissue opercular flap. A spiracular chamber is present, but the spiracle is closed and never opens during development. Also unique to extant coelacanths is the presence of a "fatty lung" or a fat-filled single-lobed vestigial lung, homologous to other fishes' swim bladders. The parallel development of a fatty organ for buoyancy control suggests a unique specialization for deep-water habitats. There are small and hard but flexible plates around the vestigial lung in adult specimens, though not around the fatty organ. The plates most likely had a regulation function for the volume of the lung. Due to the size of the fatty organ, researchers assume that it is responsible for the kidney's unusual relocation. The two kidneys, which are fused into one, are located ventrally within the abdominal cavity, posterior to the cloaca. Scientific research suggests the coelacanth must stay in cold, well-oxygenated water or else its blood cannot absorb enough oxygen. The fish seems to be very well adapted to its environment, which is seen as one of the reasons why it has the slowest evolving genome of all known vertebrates.
Biology Coelacanths are nocturnal piscivorous drift-hunters. Coelacanths are opportunistic feeders, hunting cuttlefish, squid, snipe eels, small sharks, and other fish found in their deep reef and volcanic slope habitats. Coelacanths are also known to swim head down, backwards or belly up to locate their prey, presumably using their rostral glands. To move around, they most commonly take advantage of up- or down-wellings of current and drift. Their paired fins stabilize movement through the water. While on the ocean floor, they do not use the paired fins for any kind of movement. Coelacanths generate thrust with their caudal fins for quick starts. Due to the abundance of its fins, the coelacanth has high maneuverability and can orient its body in almost any direction in the water. They have been seen doing headstands as well as swimming belly up. It is thought that the rostral organ helps give the coelacanth electroreception, which aids in movement around obstacles. They are "passive drift feeders", slowly drifting along currents with only minimal self-propulsion, eating whatever prey they encounter. Coelacanths also use their rostral organ for its electroreception to be able to detect nearby prey in low light settings.
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