Taningia danae
Species of cephalopods From Wikipedia, the free encyclopedia
Taningia danae, the Dana octopus squid, is a species of squid in the family Octopoteuthidae, the octopus squids. It is one of the largest known squid species, and it has one of the largest photophores (light organs) known in any organism, useful in the deep-sea environments that the species inhabits.
| Taningia danae | |
|---|---|
 | |
| Taningia cf. danae, Hutchison Seamounts, off Hawai'i, 2015 | |
| Scientific classification | |
| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Mollusca |
| Class: | Cephalopoda |
| Order: | Oegopsida |
| Family: | Octopoteuthidae |
| Genus: | Taningia |
| Species: | T. danae |
| Binomial name | |
| Taningia danae | |
| Synonyms | |
Discovery
Summarize
Perspective
The possible first specimen of this species was collected in 1769, when Joseph Banks, member of Captain Cook’s first voyage, spotted a massive "cuttlefish" floating in the South Pacific, off the coast of Chile. Seabirds had already damaged it, and most of the remaining carcass was prepared into a meal which Banks described as "one of the best soups [he] ever ate". However, he made sure to preserve an arm, some entrails, and the buccal mass including the beak, which would eventually enter John Hunter's collection in London; the surviving buccal mass (apparently prepared by John Hunter himself) is still part of the Hunterian Museum’s collection to this day. These specimens received multiple scientific names over the years, such as Sepia unguiculata, Enoploteuthis molina, Enoploteuthis cooki, and Cucioteuthis unguiculatus, though these names cannot be definitively linked to the modern conception of T. danae, and the species assigned to Cucioteuthis are considered nomina dubia.[3] In 1931 the name Taningia danae was coined, after the Danish fisheries biologist Åge Vedel Tåning (1890–1958), and the Danish ship Dana, which collected a more complete specimen that became the holotype of this species.[4][5][6] The taxonomic situation of Octopoteuthids in general require further revision.[3][7]
Description
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Perspective
Typical of octopus squid, T. danae is characterized by their tentacles that do not grow past the paralarval stage, giving them eight arms in adulthood like an octopus.[8][9] Taningia is separated from Octopoteuthis by adults possessing a large photophore on the tips of arm pair II (second pair from the dorsal), which are the only known photophores on the body along with the ink sac organ (Octopoteuthis has photophores on each arm-tip and spread around its body). The photophores, around the size of lemons,[10] possesses eyelid-like skin flaps which conceal the light organs when needed.[3] Each arm pair bears two rows of hooks covered by a hood of tissue that can unsheathe them when needed.[8][11]
This species is traditionally thought to be the only one within the genus and cosmopolitan, but additional species have been recognized at times. When separating different Taningia species, T. danae can be distinguished from its congeners through the blunt shape of its funnel-locking apparatus facing the mouth, arm hooks only possessing a single point at the tip, with the male not having enlarged hooks on the base of his arm pair I, the arms being 25-46% mantle length, the skin and funnel opening being smooth (without any accessory structures), along with characters of the beak.[7]
The muscular fins account for a large part of the animal's mass, around 61% being the fins, 23% being the head and arms combined, and the mantle being 14% of the total. The reproductive systems are nearly half of the visceral mass, but the single largest organ are the gills, being 29% of the visceral mass.[7]
The Dana octopus squid reaches a mantle length of 1.7 m (5.6 ft)[12] and total length of 2.3 m (7.5 ft).[13] The largest known specimen, a mature female, weighed 161.4 kg (356 lb).[8][nb a]
Biology
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Perspective
Taningia danae is considered an oceanic, mesopelagic species that likely spawns in deep waters, although its biology remains largely undocumented.[3] Most of the specimens studied globally — particularly the larger individuals — have been recovered from the guts of its predators, primarily sperm whales, but also sharks, lancetfishes, tunas, wandering albatrosses, and elephant seals.[3] Remains of T. danae have also been found washed ashore on beaches. In 2008, a mantle of T. danae was discovered by students in Bermuda's Grape Bay, while tentacle remnants were found farther along the shore.[14]
In early 2013, a 54 kg (119 lb) specimen with a length (excluding arms) of 103 cm (3.38 ft) was trawled at a depth of 240 m (790 ft) off the coast of Estaca de Bares, Galicia, Spain. It was loaned to the Spanish Institute of Oceanography.[15] A largely intact 140 kg (310 lb) specimen was found floating around 100km off the South Australian coast and sent to Flinders University in Adelaide where it was dissected in July 2024. [16]
The Dana octopus squid is thought to be extremely abundant in some regions, accounting for over 80% of the weight of sperm whale stomach contents off Iberia, and 97% of sampled sperm whales in the Tasman Sea had consumed this octopus squid.[3]
Behavior
Like other mesopelagic animals, Taningia spp. undergo diel migration, though these squid only migrate for short distances compared to other species (from 600–900 m (2,000–3,000 ft) to 240–500 m (790–1,640 ft) depth).[13]
In 2005, a Japanese research team headed by Tsunemi Kubodera managed to film T. danae in its natural habitat for the first time. The video footage, shot in deep water off Chichi-jima in the northern Pacific Ocean, shows that contrary to earlier assumptions, Taningia is an "aggressive and tenacious predator" and a powerful swimmer, capable of quickly turning by flexing its mantle, along with swimming forward and backwards by flapping its muscular fins; swimming by fin undulation has the advantage of providing consistent motion compared to the pump-pause cycle of jet propulsion. This method has been compared to the swimming style of rays, and it has been estimated that the observed octopus squid reached speeds of around 2–2.5 m (6 ft 7 in – 8 ft 2 in) per second.[13] However, specimens found in Japanese seas may be of another species of Taningia; Taningia rubea is endemic to the seas around Japan and can be easily distinguished by its longer "tail".[7]
Taningia danae is bioluminescent, akin to other octopoteuthids and squid families. Its arm photophores are some of the largest such organs known to science, the organs being compared in size to fists or lemons.[17] Black, eyelid-like membranes conceal the photophores when needed, which can be made to "blink", producing a flash of light.[5]
The 2005 video shows T. danae emitting blinding flashes of light from its arm photophores as it attacks its prey (a baited line in this instance). It is believed that this squid uses the bright flashes to disorient potential prey, as well as potentially gauging the distance to its prey, facilitating capture.[13] T. danae bioluminescence has also been suggested to be a defense mechanism; juveniles of this species have been observed moving rapidly in the direction of potential predators, as if hunting, to disorient and startle the threat with a mock attack.[18]
Different flash patterns may also serve a role in communication, perhaps for courtship or a aggressive display relating to territory; observed squid made long and short light emissions in response to a double-torch array mounted to the rig, which may have been an attempt at communication towards the rig as the observed squid did not seem aggressive. Due to a lack of response by the torch-array, the squid moved on.[13]
In 2012, T. danae was filmed twice more during a search for the giant squid for the Discovery Channel Special, Monster Squid: The Giant Is Real.[19][clarification needed]
Trophic ecology
Taningia danae appears to occupy a high trophic level, at least in the Southern Ocean ecosystem. Stable isotope analysis of specimens from the Great Australian Bight suggests they primarily feed on deep-sea fishes and small squids. Fatty acid profiles of the contents of T. danae's digestive gland were found to be similar to whole homogenized samples of deep-sea fishes like Electrona carlsbergi, Epigonus lenimen, and Lepidorhynchus denticulatus, supporting the hypothesis that these fishes are prey items.[20] Analysis of stomach contents from specimens retrieved off the coast of Spain has found blue whiting (Micromesistius poutassou) vertebrae, Gonatus sp. tentacle hooks, and integuments from crustaceans, providing direct evidence of their diet.[21]
Their carbon isotope ratios indicate they likely live in the Southern Ocean but may travel to continental shelf-slope environments like the Great Australian Bight, possibly during seasonal upwelling events. The presence of copepod fatty acid biomarkers in T. danae tissues further suggests they feed within a copepod-myctophid-squid food chain common in the Southern Ocean. T. danae appears to function as a link between deep-sea and shelf-slope environments, contributing to the transport of nutrients and energy between these different marine ecosystems.[20]
T. danae muscle tissues contain high levels of essential fatty acids EPA (20:5ω3) and DHA (22:6ω3), making them a nutrient source for predators such as sperm whales, seabirds, and seals. While T. danae has a relatively low energy density per gram (approximately 2.25 kJ/g) compared to other Southern Ocean fish and squid species, their large body size means individual specimens contain substantial energy. The whole-body energy content of a large T. danae individual (161 kg) can reach up to 362,250 kJ, making it one of the most calorically rich prey items in the Southern Ocean and an efficient food source for large predators like sperm whales.[20]
15N ratios showed that this squid is a top predator.[22][clarification needed] In turn, they are eaten by the sperm whale, a prolific predator of squid.[23][24][25] Other predators include the pygmy sperm whale,[26][27] beaked whales such as the Cuvier's and southern bottlenose whales,[28][29][30] dolphins such as the short-finned pilot whale, Risso's and Fraser's dolphins,[28][31][32] northern elephant seals,[33] ground sharks such as the tiger, blue, and scalloped hammerhead sharks,[34][3] dogfish such as the Portuguese dogfish and sleeper sharks,[34][35][36][37] swordfish,[38] and scavenging tube-nosed seabirds, such as the Bulwer's petrel, the black-browed, Laysan, and wandering albatrosses.[39][40][41]
Reproduction
Taningia danae employs a unique reproductive strategy known as spermatangium implantation, facilitated by the presence of an extendable terminal organ/penis (unlike the hectocotylus of many other cephalopods).[21] During mating, the male uses either its beak or arm hooks to make incisions in the female's tissue, into which it implants spermatophores — packets containing sperm. While spermatangium implantation is observed in several squid species, T. danae is unusual in its use of physical incisions for implantation. In most other squids, females possess specialized structures or receptacles for receiving spermatophores, making T. danae’s method notably distinct.[42][7] These incisions, typically 30–65 mm in length, are usually found in the head, neck, and inner mantle tissues, particularly around the nuchal region and collar musculature. Unlike many other cephalopods, T. danae implants spermatangia deep within muscle layers rather than attaching them externally. Some spermatangia may implant autonomously, likely aided by enzymes or filament-like structures that help them penetrate the tissue. Due to the physical trauma involved in this process, mating may pose a risk of injury to the male, and there is speculation that females may sometimes engage in cannibalism.[42]
The arm hooks develop after the paralarva reaches 5 mm (0.20 in) ML, along with a single photophore on the ink sac,[8] which is thought to be a counter-illumination mechanism in the relatively transparent juveniles.[3] The paralarvae have robust tentacular stalks which disappear at 38 mm (1.5 in) ML, leaving the adult squid with eight arms.[8] A post-larval juvenile 55.6 mm (2.19 in) ML was captured off the coast of Algeria, being the first Mediterranean record of this species.[43] Females begin to sexually mature at 200–400 mm (7.9–15.7 in) ML, with the smallest specimen known to have spawned being 882 mm (34.7 in) ML.[7]
See also
- Thysanoteuthis rhombus, a species somewhat similar in size and appearance
Notes
References
Further reading
External links
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