Lantern Fishes
Kingdom:
Animalia
Phylum:
Chordata
Chordata
Class:
Actinopterygii
Actinopterygii
Order:
Myctophiformes
Myctophiformes
Family:
Myctophidae
Lanternfishes are small, deep sea fish of the large family Myctophidae. One of two families in the order Myctophiformes, the Myctophidae are represented by 246 species in 33 genera, having a circumglobal distribution. They are aptly named after their conspicuous use of bioluminescence. Their sister family, the Neoscopelidae, is much fewer in number but superficially very similar; at least one neoscopelid shares the common name 'lanternfish': The large-scaled lantern fish, Neoscopelus macrolepidotus.
Sampling via deep trawling indicates that, together with the bristlemouths (Gonostomatidae) and lightfishes (Phosichthyidae), lanternfish account for as much as 90% of all deep sea fish biomass. Indeed, lanternfish are among the most widely distributed, populous, and diverse of all vertebrates, playing an important ecological role as prey for larger organisms. With an estimated global biomass of 550 - 660 million metric tonnes, several times the entire world fisheries catch, lanternfish also account for much of the biomass responsible for the deep scattering layer of the world's oceans. In the Southern Ocean, Myctophids provide an alternative food resource to krill for predators such as squid and the King Penguin. Although plentiful and prolific, currently only a few commercial lanternfish fisheries exist: These include limited operations off South Africa, in the sub-Antarctic, and in the Gulf of Oman.
Myctophid morphology is typified by a slender, compressed body covered in small, silvery deciduous cycloid scales (ctenoid in four species), a large bluntly rounded head, large elliptical to round lateral eyes (dorsolateral in Protomyctophum species), and a large terminal mouth with jaws closely set with rows of small teeth. The fins are generally small, with a single high dorsal fin, an adipose fin, and an anal fin—supported by a cartilaginous plate at its base—originating under or slightly behind the posterior end of the dorsal fin; the caudal fin is forked. The pectoral fins, usually with eight rays, may be large and well-developed to small and degenerate, or completely absent in a few species; the pectorals are greatly elongated in others, such as Lampanyctus species. The gas bladder is present in most lanternfish, but it degenerates or fills with lipids during the maturation of a few species. The lateral line is uninterrupted.
Lanternfish are well-known for their diel vertical migrations: during daylight hours most species remain within the gloomy bathypelagic zone, between 300 – 1,200 m depth; but towards sundown the fish begin to rise into the epipelagic zone, between 10 and 100 m depth. The lanternfish are thought to do this in order to avoid predation, and because they are following the diel vertical migrations of zooplankton upon which the lanternfish feed. After a night spent feeding in the surface layers of the water column, the lanternfish begin to descend back into the lightless depths and are gone by daybreak. Most species remain near to the coast, schooling over the continental slope. Different species are known to segregate themselves by depth, forming dense, discrete conspecific layers — this is believed to be a means of avoiding interspecies competition. Due to the lanternfishes' gas bladders, these layers are visible on sonar scans and give the impression of a "false bottom": this is the so-called deep-scattering layer that so perplexed early oceanographers.
It should be noted that there is great variability in migration patterns within the family. Some deeper-living species may not migrate at all, while others may do so only sporadically. Migration patterns may also be dependent on life history stage, sex, latitude, and season.
The arrangements of lanternfish photophores are different for each species, so it is assumed that their bioluminescence plays a role in intraspecies communication, specifically in shoaling and courtship behaviour. The concentration of the photophores on the flanks of the fish also indicate the light's use as camouflage: in a strategy termed counterillumination, the lanternfish regulate the brightness of the bluish light emitted by their photophores to match the ambient light level above, effectively masking the lanternfishes' silhouette when viewed from below.
A major source of food for many marine animals, lanternfish are an important link in the food chain of many local ecosystems, being heavily preyed upon by cetaceans, including whales and dolphins; large pelagic fish such as tuna and sharks; grenadiers and other deep-sea fish (including other lanternfish); pinnipeds; sea birds, notably penguins; and large squid such as the jumbo squid, Dosidicus gigas.
Myctophidae
Lanternfishes are small, deep sea fish of the large family Myctophidae. One of two families in the order Myctophiformes, the Myctophidae are represented by 246 species in 33 genera, having a circumglobal distribution. They are aptly named after their conspicuous use of bioluminescence. Their sister family, the Neoscopelidae, is much fewer in number but superficially very similar; at least one neoscopelid shares the common name 'lanternfish': The large-scaled lantern fish, Neoscopelus macrolepidotus.
Sampling via deep trawling indicates that, together with the bristlemouths (Gonostomatidae) and lightfishes (Phosichthyidae), lanternfish account for as much as 90% of all deep sea fish biomass. Indeed, lanternfish are among the most widely distributed, populous, and diverse of all vertebrates, playing an important ecological role as prey for larger organisms. With an estimated global biomass of 550 - 660 million metric tonnes, several times the entire world fisheries catch, lanternfish also account for much of the biomass responsible for the deep scattering layer of the world's oceans. In the Southern Ocean, Myctophids provide an alternative food resource to krill for predators such as squid and the King Penguin. Although plentiful and prolific, currently only a few commercial lanternfish fisheries exist: These include limited operations off South Africa, in the sub-Antarctic, and in the Gulf of Oman.
Myctophid morphology is typified by a slender, compressed body covered in small, silvery deciduous cycloid scales (ctenoid in four species), a large bluntly rounded head, large elliptical to round lateral eyes (dorsolateral in Protomyctophum species), and a large terminal mouth with jaws closely set with rows of small teeth. The fins are generally small, with a single high dorsal fin, an adipose fin, and an anal fin—supported by a cartilaginous plate at its base—originating under or slightly behind the posterior end of the dorsal fin; the caudal fin is forked. The pectoral fins, usually with eight rays, may be large and well-developed to small and degenerate, or completely absent in a few species; the pectorals are greatly elongated in others, such as Lampanyctus species. The gas bladder is present in most lanternfish, but it degenerates or fills with lipids during the maturation of a few species. The lateral line is uninterrupted.
Lanternfish are well-known for their diel vertical migrations: during daylight hours most species remain within the gloomy bathypelagic zone, between 300 – 1,200 m depth; but towards sundown the fish begin to rise into the epipelagic zone, between 10 and 100 m depth. The lanternfish are thought to do this in order to avoid predation, and because they are following the diel vertical migrations of zooplankton upon which the lanternfish feed. After a night spent feeding in the surface layers of the water column, the lanternfish begin to descend back into the lightless depths and are gone by daybreak. Most species remain near to the coast, schooling over the continental slope. Different species are known to segregate themselves by depth, forming dense, discrete conspecific layers — this is believed to be a means of avoiding interspecies competition. Due to the lanternfishes' gas bladders, these layers are visible on sonar scans and give the impression of a "false bottom": this is the so-called deep-scattering layer that so perplexed early oceanographers.
It should be noted that there is great variability in migration patterns within the family. Some deeper-living species may not migrate at all, while others may do so only sporadically. Migration patterns may also be dependent on life history stage, sex, latitude, and season.
The arrangements of lanternfish photophores are different for each species, so it is assumed that their bioluminescence plays a role in intraspecies communication, specifically in shoaling and courtship behaviour. The concentration of the photophores on the flanks of the fish also indicate the light's use as camouflage: in a strategy termed counterillumination, the lanternfish regulate the brightness of the bluish light emitted by their photophores to match the ambient light level above, effectively masking the lanternfishes' silhouette when viewed from below.
A major source of food for many marine animals, lanternfish are an important link in the food chain of many local ecosystems, being heavily preyed upon by cetaceans, including whales and dolphins; large pelagic fish such as tuna and sharks; grenadiers and other deep-sea fish (including other lanternfish); pinnipeds; sea birds, notably penguins; and large squid such as the jumbo squid, Dosidicus gigas.
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