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The vampire squid (Vampyroteuthis infernalis, lit. "vampire squid from Hell") is a small cephalopod found throughout temperate and tropical oceans in extreme deep sea conditions. Unique retractile sensory filaments justify the vampire squid's placement in its own order, Vampyromorphida, as it shares similarities with both octopuses and squid. As a phylogenetic relict, it is the only known surviving member of its order. The first specimens were collected on the Valdivia Expedition and they were originally described as an octopus in 1903 by German teuthologist Carl Chun, but later assigned to a new order together with several extinct taxa.

Contents

 * 1 Description
 * 2 Habitat and Adaptations
 * Aphotic Habitat
 * Evading Predators
 * 3 Behavior
 * Development
 * Breeding
 * Foraging
 * 4 Relationships
 * 5 Management and Conservation
 * 6 Notes
 * 7 References
 * 8 External links
 * 8.1Images

Description [ edit]
The vampire squid can reach a maximum total length around 30 cm (1 ft). Its 15-cm (6-in) gelatinous body varies in color from velvety jet-black to pale reddish, depending on location and lighting conditions. A webbing of skin connects its eight arms, each lined with rows of fleshy spines or cirri; the inner side of this "cloak" is black. Only the distal halves (farthest from the body) of the arms have suckers. Its limpid, globular eyes, which appear red or blue, depending on lighting, are proportionately the largest in the animal kingdom at 2.5 cm (1 in) in diameter. Its eyes lack a cornea, which is typical among pelagic organisms. The name of the animal was inspired by its dark color, cloaklike webbing, and red eyes, rather than habit—it feeds on detritus, not blood.

Mature adults have a pair of small fins projecting from the lateral sides of the mantle. These earlike fins serve as the adult's primary means of propulsion: vampire squid move through the water by flapping their fins. Their beaklike jaws are white. Within the webbing are two pouches wherein the tactile velar filaments are concealed. The filaments are analogous to a true squid's tentacles, extending well past the arms; but differ in origin, and represent the pair that was lost by the ancestral octopus.

The vampire squid is almost entirely covered in light-producing organs called photophores, capable of producing disorienting flashes of light ranging in duration from fractions of a second to several minutes. The intensity and size of the photophores can also be modulated. Appearing as small, white discs, the photophores are larger and more complex at the tips of the arms and at the base of the two fins, but are absent from the undersides of the caped arms. Two larger, white areas on top of the head were initially believed to also be photophores, but are now identified as photoreceptors.

The chromatophores (pigment organs) common to most cephalopods are poorly developed in the vampire squid. Although the animal is, therefore, incapable of changing its skin color in the dramatic fashion of shallow-dwelling cephalopods, such ability would not be useful at the lightless depths where it lives.

Aphotic Habitat
The vampire squid is an extreme example of a deep sea cephalopod, thought to reside at aphotic (lightless) depths from 600 to 900 meters (2,000 to 3,000 ft) or more. Within this region of the world's oceans is a discrete habitat known as the oxygen minimum zone. Within the zone, the saturation of oxygen is too low to support aerobic metabolism in most complex organisms. Nonetheless, the vampire squid is able to live and breathe normally in the minimum zone at oxygen saturations as low as 3%, an ability that few other animals possess.

To cope with life in the suffocating depths, vampire squids have developed several interesting adaptations. Of all deep-sea cephalopods, their mass-specific metabolic rate is the lowest. Their blue blood's hemocyanin binds and transports oxygen more efficiently than in other cephalopods, aided by gills with an especially large surface area. The vampire squid has a branchial canal (thought to help collect seawater through the gills) located at the base of the gill surface. The animals have weak musculature, but maintain agility and buoyancy with little effort because of sophisticated statocysts (balancing organs akin to a human's inner ear) and ammonium-rich gelatinous tissues closely matching the density of the surrounding seawater.

Evading Predators
Unlike their relatives living in more hospitable climates, deep-sea cephalopods cannot afford to expend energy in protracted flight. Given their low metabolic rate and the low density of prey at such depths, vampire squids must use innovative predator avoidance tactics to conserve energy. Their bioluminescence is combined with the writhing of glowing arms, erratic movements, and escape trajectories, making it difficult for a predator to identify a single target. The vampire squid's lack of a buccal crown (an umbrella-like structure near the mouth) makes the organism effective at swift avoidance of sudden predatory pressures.

In a threat response called the "pumpkin" or "pineapple" posture, the vampire squid inverts its caped arms back over the body, presenting an ostensibly larger form covered in fearsome-looking though harmless spines (called cirri). The underside of the cape is heavily pigmented, masking most of the body's photophores. The glowing arm tips are clustered together far above the animal's head, diverting attack away from critical areas. If a predator were to bite off an arm tip, the vampire squid can regenerate it.

Like many deep-sea cephalopods, the vampire squid lacks ink sacs. If disturbed, it will curl its arms up outwards and wrap them around its body, turning itself inside-out in a way, exposing spiny projections. If highly agitated, it may eject a sticky cloud of bioluminescent mucus containing innumerable orbs of blue light from the arm tips. This luminous barrage, which may last nearly 10 minutes, would presumably serve to dazzle would-be predators and allow the vampire squid to disappear into the blackness without the need to swim far. The display is made only if the animal is very agitated because regenerating the mucus is metabolically costly.

Observed Behavior
What behavioral data are known have been gleaned from ephemeral encounters with ROVs; animals are often injured during capture, and survive up to two months in aquaria.[citation needed] An artificial environment makes reliable observation of non-defensive behavior difficult. In May 2014, Monterey Bay Aquarium (California, United States) became the first to ever put this species on display.

With their long velar filaments deployed, vampire squids have been observed drifting along in the deep, black ocean currents. If the filaments contact an entity, or if vibrations impinge upon them, the animals investigate with rapid acrobatic movements. They are capable of swimming at speeds equivalent to two body lengths per second, with an acceleration time of five seconds. However, their weak muscles limit stamina considerably.

Development
Few specifics are known regarding the ontogeny of the vampire squid. Their development progresses through three morphologic forms: the very young animals have a single pair of fins, an intermediate form has two pairs, and the mature form again has one. At their earliest and intermediate phases of development, a pair of fins is located near the eyes; as the animal develops, this pair gradually disappears as the other pair develops. As the animals grow and their surface area to volume ratio drops, the fins are resized and repositioned to maximize gait efficiency. Whereas the young propel themselves primarily by jet propulsion, mature adults find flapping their fins to be the most efficient means. This unique ontogeny caused confusion in the past, with the varying forms identified as several species in distinct families.

Hatchlings are about 8 mm in length and are well-developed miniatures of the adults, with some differences. Their arms lack webbing, their eyes are smaller, and their velar filaments are not fully formed. The hatchlings are transparent and survive on a generous internal yolk for an unknown period before they begin to actively feed.

Breeding
If hypotheses may be drawn from knowledge of other deep-sea cephalopods, the vampire squid likely reproduces slowly by way of a small number of large eggs. Growth is slow, as nutrients are not abundant at depths frequented by the animals. The vastness of their habitat and its sparse population make procreative encounters a fortuitous event. The female may store a male's hydraulically implanted spermatophore (a tapered, cylindrical satchel of sperm) for long periods before she is ready to fertilize her eggs. Once she does, she may need to brood over them for up to 400 days before they hatch. Their reproductive strategy appears to be of the iteroparous type, which is an exception amongst the otherwise semelparous Coleoidea. It has been hypothesized that the iteroparous lifestyle of the vampire squid has evolved with the squid's relaxed lifestyle. With iteroparity often seen in organisms with high adult survival rates, such as the vampire squid, many low-cost reproductive cycles would be expected for the species.

Foraging
They have eight arms but lack feeding tentacles, and instead use two retractile filaments in order to capture food. They combine the waste with mucus secreted from suckers to form balls of food. The smaller animals frequent much deeper waters, perhaps feeding on marine snow, including the remains of gelatinous zooplankton (such as salps, larvaceans, and medusae jellies) and complete copepods, ostracods, amphipods, and isopods. The mature vampire squid is also thought to be an opportunistic hunter of larger prey as fish bones, other squid flesh, and gelatinous matter has been recorded in mature vampire squid stomachs.

Phylogeny
The Vampyromorphida are characterized by derived characters such as the possession of photophores and of two velar filaments which are most probably modified arms. It also shares the inclusion of an internal gladius with other coleoids, including squid, and eight webbed arms with cirrate octopods.

Vampyroteuthis shares its eight cirrate arms with the Cirrata, in which lateral cirri, or filaments, alternate with the suckers. Vampyroteuthis differs in that suckers are present only on the distal half of the arms while cirri run the entire length. In cirrate octopods suckers and cirri run and alternate on the entire length. Also, a close relationship between Vampyroteuthis and the Jurassic-Cretaceous Loligosepiina is indicated by the similarity of their gladiuses, the internal stiffening structure. However, the inclusion of Vampyronassa rhodanica from the middle Jurassic La Voulte-sur-Rhône of France as a vampyroteuthid turns out to be rather doubtful.

The supposed vampyromorphids from the Kimmeridgian-Tithonian (156–146 mya) of Solnhofen, Plesioteuthis prisca, Leptoteuthis gigas, and Trachyteuthis hastiformis, cannot be positively assigned to this group; they are large species (from 35 cm in P. prisca to > 1 m in L. gigas) and show features not found in vampyromorphids, being somewhat similar to the true squids, Teuthida.

The vampire squid is the known surviving member of its order, Vampyromorphida. However, there are more than two hundred species in the surrounding, similar orders, leaving a puzzle to be researched.

Genetic Markers
The mitochondrial genome structure of the vampire squid is identical to that of the Incirrata, common octopus. Therefore, the vampire squid more similar to that of the polyplacophoran Katharina tunicata, than to the previously thought cephalopod Nautilus macromphalus.

Predators
Vampire squids have been found among the stomach contents of large, deepwater fish, including giant grenadiers, and deep-diving mammals, such as whales and sea lions.

Management and Conservation[ edit]
At this time, the vampire squid population is not considered to be threatened. The organism is also not believed to be dangerous to humans in any way.

References[ edit]

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Golikov, A.V. ; Ceia, F. R.; Sabirov, R. M.; Ablett, J. D.; Gleadall, I.  G.; Gudmundsson, G.; Hoving, H. J.; Judkins, H.; Palsson, J. ; Reid, A. L.; Rosas-Luis, R.; Shea, E. K.; Schwarz, R.; Xavier, J. C.. (2019). The first global deep-sea stable isotope assessment reveals the unique trophic ecology of Vampire Squid Vampyroteuthis infernalis (Cephalopoda). Nature, 9(19099)

Lindsay, D.J., Maruyama, T., Oshima, T., Tsuchiya, K., Yamagishi, A.,Yokobori, S., & Yoshida, M. (2007). Mitochondrial genome structure and evolution in the living fossil vampire squid, Vampyroteuthis infernalis, and extant cephalopods. Molecular Phylogenetic Evolution, 44 (2), 898-910.