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| The Common Octopus, Octopus vulgaris.|
The Common Octopus, Octopus vulgaris.
The octopus (pronounced /ˈɒktəpəs/, from Greek ὀκτάπους (oktapous), "eight-footed", with plural forms: octopuses [ˈɒktəpʊsɪz], octopi [ˈɒktəpaɪ], or octopodes [ˌɒkˈtəʊpədiːz], see below) is a cephalopod of the order Octopoda that inhabits many diverse regions of the ocean, especially coral reefs. The term may also refer to only those creatures in the genus Octopus. In the larger sense, there are around 300 recognized octopus species, which is over one-third of the total number of known cephalopod species.
An octopus has eight flexible arms, which trail behind it as it swims. Most octopuses have no internal or external skeleton, allowing them to squeeze through tight places. An octopus has a hard beak, with its mouth at the center point of the arms. Octopuses are highly intelligent, probably the most intelligent invertebrates. They are known to build "forts" and "traps" in the wild, and for rearranging tanks and burying other animals alive in domestication[How to reference and link to summary or text]. For this reason, they are quite notorious among aquarium operators. For defense against predators, they hide, flee quickly, expel ink, or use color-changing camouflage. Octopuses are bilaterally symmetrical, like other cephalopods, with two eyes and four pairs of arms.
Octopuses are characterized by their eight arms (as distinct from the tentacles found in squid and cuttlefish), usually bearing suction cups. These arms are a type of muscular hydrostat. Unlike most other cephalopods, the majority of octopuses – those in the suborder most commonly known, Incirrina – have almost entirely soft bodies with no internal skeleton. They have neither a protective outer shell like the nautilus, nor any vestige of an internal shell or bones, like cuttlefish or squid. A beak, similar in shape to a parrot's beak, is the only hard part of their body. This enables them to squeeze through very narrow slits between underwater rocks, which is very helpful when they are fleeing from morays or other predatory fish. The octopuses in the less familiar Cirrina suborder have two fins and an internal shell, generally reducing their ability to squeeze into small spaces.
Octopuses have a relatively short life expectancy, and some species live for as little as six months. Larger species, such as the North Pacific Giant Octopus, may live for up to five years under suitable circumstances. However, reproduction is a cause of death: males can only live for a few months after mating, and females die shortly after their eggs hatch. They neglect to eat during the (roughly) one month period spent taking care of their unhatched eggs, but they don't die of starvation. Endocrine secretions from the two optic glands are the cause of genetically-programmed death (and if these glands are surgically removed, the octopus may live many months beyond reproduction, until she finally starves).
Octopuses have three hearts. Two pump blood through each of the two gills, while the third pumps blood through the body. Octopus blood contains the copper-rich protein hemocyanin for transporting oxygen. Although less efficient under normal conditions than the iron-rich hemoglobin of vertebrates, in cold conditions with low oxygen pressure, hemocyanin oxygen transportation is more efficient than hemoglobin oxygen transportation. The hemocyanin is dissolved in the plasma instead of being carried within red blood cells and gives the blood a blue color. Octopuses draw water into their mantle cavity where it passes through its gills. As mollusks, octopuses have gills that are finely divided and vascularized outgrowths of either the outer or the inner body surface.
- Main article: Cephalopod intelligence
Octopuses are highly intelligent, likely more so than any other order of invertebrates. The exact extent of their intelligence and learning capability is much debated among biologists, but maze and problem-solving experiments have shown that they do have both short- and long-term memory. Their short lifespans limit the amount they can ultimately learn. There has been much speculation to the effect that almost all octopus behaviors are independently learned rather than instinct-based, although this remains largely unproven. They learn almost no behaviors from their parents, with whom young octopuses have very little contact.
An octopus has a highly complex nervous system, only part of which is localized in its brain. Two-thirds of an octopus' neurons are found in the nerve cords of its arms, which have a remarkable amount of autonomy. Octopus arms show a wide variety of complex reflex actions arising on at least three different levels of the nervous system. Some octopuses, such as the Mimic Octopus, will move their arms in ways that emulate the movements of other sea creatures.
In laboratory experiments, octopuses can be readily trained to distinguish between different shapes and patterns. They have been reported to practice observational learning, although the validity of these findings is widely contested on a number of grounds. Octopuses have also been observed in what some have described as play: repeatedly releasing bottles or toys into a circular current in their aquariums and then catching them. Octopuses often break out of their aquariums and sometimes into others in search of food. They have even boarded fishing boats and opened holds to eat crabs.
In some countries, octopuses are on the list of experimental animals on which surgery may not be performed without anesthesia. In the UK, cephalopods such as octopuses are regarded as honorary vertebrates under the Animals (Scientific Procedures) Act 1986 and other cruelty to animals legislation, extending to them protections not normally afforded to invertebrates.
An octopus' main (primary) defense is to hide, either not to be seen at all, or not to be detected as an octopus. Octopuses have several secondary defenses (defenses they use once they have been seen by a predator). The most common secondary defense is fast escape. Other defenses include the use of ink sacs, camouflage, and autotomising limbs.
Most octopuses can eject a thick blackish ink in a large cloud to aid in escaping from predators. The main colouring agent of the ink is melanin, which is the same chemical that gives humans their hair and skin colour. This ink cloud is thought to dull smell, which is particularly useful for evading predators that are dependent on smell for hunting, such as sharks. Ink clouds of some species might serve as pseudomorphs, or decoys that the predator attacks instead.
An octopus' camouflage is aided by certain specialized skin cells which can change the apparent color, opacity, and reflectiveness of the epidermis. Chromatophores contain yellow, orange, red, brown, or black pigments; most species have three of these colors, while some have two or four. Other color-changing cells are reflective iridophores, and leucophores (white). This color-changing ability can also be used to communicate with or warn other octopuses. The very venomous blue-ringed octopus becomes bright yellow with blue rings when it is provoked. Octopuses can use muscles in the skin to change the texture of their mantle in order to achieve a greater camouflage. In some species the mantle can take on the spiky appearance of seaweed, or the scraggly, bumpy texture of a rock, among other disguises. However in some species skin anatomy is limited to relatively patternless shades of one color, and limited skin texture. It is thought that octopuses that are day-active and/or live in complex habitats such as coral reefs have evolved more complex skin than their nocturnal and/or sand-dwelling relatives.
A few species, such as the Mimic Octopus, have a fourth defense mechanism. They can combine their highly flexible bodies with their color changing ability to accurately mimic other, more dangerous animals such as lionfish, sea snakes, and eels.
When octopuses reproduce, males use a specialized arm called a hectocotylus to insert spermatophores (packets of sperm) into the female's mantle cavity. The hectocotylus in benthic octopuses is usually the third right arm. Males die within a few months of mating. In some species, the female octopus can keep the sperm alive inside her for weeks until her eggs are mature. After they have been fertilized, the female lays about 200,000 eggs (this figure dramatically varies between families, genera, species and also individuals). The female hangs these eggs in strings from the ceiling of her lair, or individually attaches them to the substrate depending on the species. The female cares for the eggs, guarding them against predators, and gently blowing currents of water over them so that they get enough oxygen. The female does not eat during the roughly one-month period spent taking care of the unhatched eggs. At around the time the eggs hatch, the mother dies and the young larval octopuses spend a period of time drifting in clouds of plankton, where they feed on copepods, larval crabs and larval starfish until they are ready to sink down to the bottom of the ocean, where the cycle repeats itself. In some deeper dwelling species, the young do not go through this period. This is a dangerous time for the larval octopuses; as they become part of the plankton cloud they are vulnerable to many plankton eaters.
Octopuses have keen eyesight. Although their slit-shaped pupils might be expected to afflict them with astigmatism, it appears that this is not a problem in the light levels in which an octopus typically hunts.[How to reference and link to summary or text] They do not appear to have color vision, although they can distinguish the polarization of light. Attached to the brain are two special organs, called statocysts, that allow the octopus to sense the orientation of its body relative to horizontal. An autonomic response keeps the octopus' eyes oriented so that the pupil slit is always horizontal.
Octopuses also have an excellent sense of touch. An octopus' suction cups are equipped with chemoreceptors so that the octopus can taste what it is touching. The arms contain tension sensors so that the octopus knows whether its arms are stretched out. However, the octopus has a very poor proprioceptive sense. The tension receptors are not sufficient for the octopus brain to determine the position of the octopus' body or arms. (It is not clear that the octopus brain would be capable of processing the large amount of information that this would require; the flexibility of an octopus' arms is much greater than that of the limbs of vertebrates, which devote large areas of cerebral cortex to the processing of proprioceptive inputs.) As a result, the octopus does not possess stereognosis; that is, it does not form a mental image of the overall shape of the object it is handling. It can detect local texture variations, but cannot integrate the information into a larger picture.
The neurological autonomy of the arms means that the octopus has great difficulty learning about the detailed effects of its motions. The brain may issue a high-level command to the arms, but the nerve cords in the arms execute the details. There is no neurological path for the brain to receive feedback about just how its command was executed by the arms; the only way it knows just what motions were made is by observing the arms visually.
Octopuses move about by crawling or swimming. Their main means of slow travel is crawling, with some swimming. Jet propulsion is their fastest means of locomotion, followed by swimming and bipedal walking.
They crawl by walking on their arms, usually on many at once, on both solid and soft surfaces, while supported in water. In 2005 it was reported that some octopuses (Adopus aculeatus and Amphioctopus marginatus under current taxonomy) can walk on two arms, while at the same time resembling plant matter. This form of locomotion allows these octopuses to move quickly away from a potential predator while possibly not triggering that predator's search image for octopus (food). Octopuses lack bones and are extremely vulnerable to predators.
- See also: Cephalopod size
The North Pacific Giant Octopus, Enteroctopus dofleini, is often cited as the largest octopus species. Adults usually weigh around 15 kg (33 lb), with an arm span of up to 4.3 m (14 ft). The largest specimen of this species to be scientifically documented was an animal with a live mass of 71 kg (156.5 lb). The alternative contender is the Seven-arm Octopus, Haliphron atlanticus, based on a 61 kg (134 lb) carcass estimated to have a live mass of 75 kg (165 lb). However, there are a number of questionable size records that would suggest E. dofleini is the largest of all octopus species by a considerable margin; one such record is of a specimen weighing 272 kg (600 lb) and having an arm span of 9 m (30 ft).
There are three forms of the plural of octopus; namely, octopuses, octopi, and octopodes. Currently, octopuses is the most common form in the UK as well as the US; octopodes is rare, and octopi is often objectionable.
The Oxford English Dictionary (2004 update) lists octopuses, octopi and octopodes (in that order); it labels octopodes "rare", and notes that octopi derives from the mistaken assumption that octōpūs is a second declension Latin noun, which it is not. Rather, it is (Latinized) Greek, from oktṓpous (ὀκτώπους), gender masculine, whose plural is oktṓpodes (ὀκτώποδες). If the word were native to Latin, it would be octōpēs ('eight-foot') and the plural octōpedes, analogous to centipedes and mīllipedes, as the plural form of pēs ('foot') is pedes. In modern Greek, it is called khtapódi (χταπόδι), gender neuter, with plural form khtapódia (χταπόδια).
Chambers 21st Century Dictionary and the Compact Oxford Dictionary list only octopuses, although the latter notes that octopodes is "still occasionally used"; the British National Corpus has 29 instances of octopuses, 11 of octopi and 4 of octopodes. Merriam-Webster 11th Collegiate Dictionary lists octopuses and octopi, in that order; Webster's New World College Dictionary lists octopuses, octopi and octopodes (in that order).
The term octopod (plural octopods or octopodes) is taken from the taxonomic order Octopoda but has no classical equivalent. The collective form octopus is usually reserved for animals consumed for food.
Relationship to humans Edit
Ancient peoples of the Mediterranean were aware of the octopus, as evidenced by certain artworks and designs of prehistory. For example, a stone carving found in the archaeological recovery from Bronze Age Minoan Crete at Knossos has a depiction of a fisherman carrying an octopus.
In mythology Edit
The Hawaiʻian creation myth relates that the present cosmos is only the last of a series, having arisen in stages from the wreck of the previous universe. In this account, the octopus is the lone survivor of the previous, alien universe.
As food Edit
Many species of octopus are eaten as food by human cultures around the world. The arms and sometimes other parts of the body are prepared in various ways, often depending on the species being eaten.
Care must be taken to boil the octopus properly, to rid it of slime and the smell, as well as any residual ink.
Octopus is a common ingredient in Japanese cuisine, including sushi, takoyaki, and Akashiyaki. Some small species are sometimes eaten alive as a novelty and health food (mostly in South Korea). Similarly, a live octopus may be sliced up and the legs eaten while still squirming, which they continue to do for some minutes.
Octopus is also eaten regularly in Hawai'i, many of the popular dishes being Asian in origin. Locally known by their Hawaiian or Japanese names, ("he'e" and "tako" respectively) octopus is also a popular catch used as fish bait.
Octopus is also a common food in Mediterranean cuisine and Portuguese cuisine. In Galicia, polbo á feira (fair style octopus) is a local delicacy. Restaurants which specialize or serve this dish are known as pulperías.
According to the USDA Nutrient Database (2007), cooked octopus contains approximately 139 calories per three ounce portion, and is a source of vitamin B3, B12, potassium, phosphorus, and selenium.
As pets Edit
Though octopuses can be difficult to keep in captivity, some people keep them as pets. Octopuses often escape even from supposedly secure tanks, due to their problem solving skills, mobility and lack of rigid structure.
The variation in size and life span among octopus species makes it difficult to know how long a new specimen can naturally be expected to live. That is, a small octopus may be just born or may be an adult, depending on the species. By selecting a well-known species, such as the California Two-spot Octopus, one can choose a small octopus (around the size of a tennis ball) and be confident that it is young with a full life ahead of it.
Octopuses are also quite strong for their size. Octopuses kept as pets have been known to open the covers of their aquariums and survive for a time in the air in order to get to a nearby feeder tank and gorge themselves on the fish there. They have also been known to catch and kill some species of sharks.
- Class CEPHALOPODA
- Subclass Nautiloidea: nautilus
- Subclass Coleoidea
- Superorder Decapodiformes: squid, cuttlefish
- Superorder Octopodiformes
- Order Vampyromorphida: Vampire Squid
- Order Octopoda
- Genus †Keuppia (incertae sedis)
- Genus †Palaeoctopus (incertae sedis)
- Genus †Pohlsepia (incertae sedis)
- Genus †Proteroctopus (incertae sedis)
- Genus †Styletoctopus (incertae sedis)
- Suborder Cirrina: finned deep-sea octopus
- Suborder Incirrina
- Family Amphitretidae: telescope octopus
- Family Bolitaenidae: gelatinous octopus
- Family Octopodidae: benthic octopus
- Family Vitreledonellidae: Glass Octopus
- Superfamily Argonautoida
- ↑ Oktapous, Henry George Liddell, Robert Scott, A Greek-English Lexicon, at Perseus
- ↑ Scientific Latin from Greek ὀκτώποδ-, ὀκτώπους (also ὀκτάποδ- ὀκτάπους) "eight-footed" > ὀκτώ- or ὀκτά- [combination form of ὀκτώ "eight"] and πόδ-, πούς "foot". Cf. Modern Greek χταπόδι < οκταπόδι < οκταπόδιον < ὀκτάπους.
- ↑ 
- ↑ 4.0 4.1 What is this octopus thinking?. By Garry Hamilton.
- ↑ 5.0 5.1 Is the octopus really the invertebrate intellect of the sea? By Doug Stewart. In: National Wildlife. Feb/Mar 1997, vol.35 no.2.
- ↑ 6.0 6.1 Giant Octopus—Mighty but Secretive Denizen of the Deep
- ↑ How Smart is the Octopus? Slate.
- ↑ Octopus intelligence: jar opening
- ↑ What behavior can we expect of octopuses?. By Dr. Jennifer Mather, Department of Psychology and Neuroscience, University of Lethbridge and Roland C. Anderson, The Seattle Aquarium.
- ↑ United Kingdom Animals (Scientific Procedures) act of 1986
- ↑ 11.0 11.1 Hanlon, R.T. & J.B. Messenger 1996. Cephalopod Behaviour. Cambridge University Press, Cambridge.
- ↑ Caldwell, R. L. (2005). "An Observation of Inking Behavior Protecting Adult Octopus bocki from Predation by Green Turtle (Chelonia mydas) Hatchlings." Pacific Science 59(1): 69–72.
- ↑ Meyers, Nadia. Tales from the Cryptic: The Common Atlantic Octopus. Southeastern Regional Taxonomic Center. URL accessed on 2006-07-27.
- ↑ Norman, M.D., J. Finn & T. Tregenza (2001). PDF (312 KB) Proceedings of the Royal Society 268: 1755–1758.
- ↑ Norman, M.D. & F.G.Hochberg (2005). The "Mimic Octopus" (Thaumoctopus mimicus n. gen. et sp.), a new octopus from the tropical Indo-West Pacific (Cephalopoda: Octopodidae). Molluscan Research 25: 57–70. Abstract
- ↑ 16.0 16.1 Wells. Martin John. Octopus: physiology and behaviour of an advanced invertebrate. London : Chapman and Hall ; New York : distributed in the U.S.A. by Halsted Press, 1978.
- ↑ 17.0 17.1 Locomotion by Abdopus aculeatus, C.L. Huffard 2006
- ↑ Science, vol. 307, p. 1927
- ↑ Smithsonian National Zoological Park: Giant Pacific Octopus
- ↑ Cosgrove, J.A. 1987. Aspects of the Natural History of Octopus dofleini, the Giant Pacific Octopus. M.Sc. Thesis. Department of Biology, University of Victoria (Canada), 101 pp.
- ↑ O'Shea, S. 2004. The giant octopus Haliphron atlanticus (Mollusca : Octopoda) in New Zealand waters. New Zealand Journal of Zoology 31(1): 7-13.
- ↑ O'Shea, S. 2002. Haliphron atlanticus — a giant gelatinous octopus. Biodiversity Update 5: 1.
- ↑ Norman, M. 2000. Cephalopods: A World Guide. Hackenheim, ConchBooks, p. 214.
- ↑ High, W.L. 1976. The giant Pacific octopus. U.S. National Marine Fisheries Service, Marine Fisheries Review 38(9): 17-22.
- ↑ Peters, Pam (2004). The Cambridge Guide to English Usage. Cambridge: Cambridge University Press. ISBN 0-521-62181-X, p. 388.
- ↑  (subscription required). Retrieved October 22, 2007.
- ↑ . Retrieved October 19, 2007.
- ↑  Retrieved October 19, 2007.
- ↑ C. Michael Hogan. 2007 Knossos fieldnotes, The Modern Antiquarian
- ↑ Berrin, Katherine & Larco Museum. The Spirit of Ancient Peru:Treasures from the Museo Arqueológico Rafael Larco Herrera. New York: Thames and Hudson, 199 7.
- ↑ Dixon, Roland Burrage (1916). The Mythology of All Races, Marshall Jones.
- ↑ Octopus Calories And Nutrition
- ↑ Archived Google video of an octopus catching a shark, from The Octopus Show by Mike deGruy
- Mather, J. (1992). Underestimating the octopus. New York, NY: Cambridge University Press.
- Packard, A. (1990). Reading your enemy right: Lessons from the octopus in the subtle art of self-defence. Amsterdam, Netherlands: Harwood Academic Publishers.
- Adams, K. A. (1983). Love American Style: II. "Octopoid" genitality and the medusal madonna: Journal of Psychohistory Vol 10(4) Spr 1983, 409-462.
- Adams, P. M., Hanlon, R. T., & Forsythe, J. W. (1988). Toxic exposure to ethylene dibromide and mercuric chloride: Effects on laboratory-reared octopuses: Neurotoxicology and Teratology Vol 10(6) Nov-Dec 1988, 519-523.
- Agnisola, C., Castaldo, P., & Fiorito, G. (1996). Octopus vulgaris (Mollusca, cephalopoda) as a omdel in behavioral pharmacology: A test of handling effects: Physiology & Behavior Vol 59(4-5) Apr-May 1996, 729-733.
- Akaka, W. H., & Houck, B. A. (1980). The use of an ultrasound monitor for recording locomotor activity: Behavior Research Methods & Instrumentation Vol 12(5) Oct 1980, 514-516.
- Allen, A., Michels, J., & Young, J. Z. (1986). Possible interactions between visual and tactile memories in octopus: Marine and Freshwater Behaviour and Physiology Vol 12(2) Apr 1986, 81-97.
- Anderson, R. C., & Mather, J. A. (2007). The packaging problem: Bivalve prey selection and prey entry techniques of the octopus Enteroctopus dofleini: Journal of Comparative Psychology Vol 121(3) Aug 2007, 300-305.
- Angermeier, W. F., & Dassler, K. (1992). Inhibitory learning and memory in the lesser octopus (Eledone cirrhosa): Bulletin of the Psychonomic Society Vol 30(4) Jul 1992, 309-310.
- Aronson, R. B. (1985). Ecological release in a Bahamian salt water lake: Octopus briareus (cephalopoda) and Ophiothrix oerstedii (ophiuroidea): Dissertation Abstracts International.
- Barlow, J. J., & Sanders, G. D. (1974). Intertrial interval and passive avoidance learning in Octopus vulgaris: Animal Learning & Behavior Vol 2(2) May 1974, 86-88.
- Boal, J. G., Dunham, A. W., Williams, K. T., & Hanlon, R. T. (2000). Experimental evidence for spatial learning in octopuses (Octopus bimaculoides): Journal of Comparative Psychology Vol 114(3) Sep 2000, 246-252.
- Boal, J. G., & Fenwick, J. W. (2007). Laterality in octopus eye use? : Animal Behaviour Vol 74(3) Sep 2007, e1-e2.
- Boyle, P. R. (1980). Home occupancy by male Octopus vulgaris in a large seawater tank: Animal Behaviour Vol 28(4) Nov 1980, 1123-1126.
- Bradley, E. A., & Messenger, J. B. (1977). Brightness preference in Octopus as a function of the background brightness: Marine and Freshwater Behaviour and Physiology Vol 4(4) Sep 1977, 243-251.
- Bradley, E. A., & Young, J. Z. (1975). Are there circadian rhythms in learning by Octopus? : Behavioral Biology Vol 13(4) Apr 1975, 527-531.
- Brown, E. R., Piscopo, S., De Stefano, R., & Giuditta, A. (2006). Brain and behavioural evidence for rest-activity cycles in Octopus vulgaris: Behavioural Brain Research Vol 172(2) Jul 2006, 355-359.
- Byrne, R. A., Kuba, M., & Griebel, U. (2002). Lateral asymmetry of eye use in Octopus vulgaris: Animal Behaviour Vol 64(3) Sep 2002, 461-468.
- Byrne, R. A., Kuba, M. J., & Meisel, D. V. (2004). Lateralized eye use in Octopus vulgaris shows antisymmetrical distribution: Animal Behaviour Vol 68(5) Nov 2004, 1107-1114.
- Byrne, R. A., Kuba, M. J., Meisel, D. V., Griebel, U., & Mather, J. A. (2006). Does Octopus vulgaris have preferred arms? : Journal of Comparative Psychology Vol 120(3) Aug 2006, 198-204.
- Byrne, R. A., Kuba, M. J., Meisel, D. V., Griebel, U., & Mather, J. A. (2006). Octopus arm choice is strongly influenced by eye use: Behavioural Brain Research Vol 172(2) Jul 2006, 195-201.
- Cheng, M. W., & Caldwell, R. L. (2000). Sex identification and mating in the blue-ringed octopus, Hapalochlaena lunulata: Animal Behaviour Vol 60(1) Jul 2000, 27-33.
- Cigliano, J. A. (1993). Dominance and den use in -I Octopus bimaculoides: Animal Behaviour Vol 46(4) Oct 1993, 677-684.
- Cigliano, J. A. (1995). Assessment of the mating history of female pygmy octopuses and a possible sperm competition mechanism: Animal Behaviour Vol 49(3) Mar 1995, 849-851.
- Cobb, C. S., Pope, S. K., & Williamson, R. (1995). Circadian rhythms to light-dark cycles in the lesser octopus, Eledone cirrhosa: Marine and Freshwater Behaviour and Physiology Vol 26(1) Aug 1995, 47-57.
- Cobb, C. S., Williamson, R., & Pope, S. K. (1995). The responses to the epistellar photoreceptors to light and their effect on circadian rhythms in the lesser octopus, -I Eledone cirrhosa: Marine and Freshwater Behaviour and Physiology Vol 26(1) Aug 1995, 59-69.
- Dewsbury, D. A. (1978). Review of Octopus: Physiology and behaviour of an advanced invertebrate: PsycCRITIQUES Vol 23 (10), Oct, 1978.
- Di Cristo, C., Delli Bovi, P., & Di Cosmo, A. (2003). Role of FMRFamide in the reproduction of Octopus vulgaris: Molecular analysis and effect on visual input: Peptides Vol 24(10) Oct 2003, 1525-1532.
- Domagk, G. F., Alexander, W. R., & Heermann, K. H. (1976). Transfer of learned tactile discrimination in Octopus vulgaris by means of brain extracts: Negative results: Journal of Biological Psychology Vol 18(1) Jul 1976, 15-17.
- Edelman, D. B., Baars, B. J., & Seth, A. K. (2005). Identifying hallmarks of consciousness in non-mammalian species: Consciousness and Cognition: An International Journal Vol 14(1) Mar 2005, 169-187.
- Fiorito, G., Biederman, G. B., Davey, V. A., & Gherardi, F. (1998). The role of stimulus preexposure in problem solving by Octupus vulgaris: Animal Cognition Vol 1(2) 1998, 107-112.
- Fiorito, G., & Gherardi, F. (1999). Prey-handling behaviour of Octopus vulgaris (Mollusca, Cephalopoda) on Bivalve preys: Behavioural Processes Vol 46(1) May 1999, 75-88.
- Fiorito, G., & Scotto, P. (1992). Observational learning in Octopus vulgaris: Science Vol 256(5056) Apr 1992, 545-547.
- Fiorito, G., von Planta, C., & Scotto, P. (1990). Problem solving ability of Octopus vulgaris Lamarck (Mollusca, Cephalopoda): Behavioral & Neural Biology Vol 53(2) Mar 1990, 217-230.
- Greenwood, J. J. (1991). Marine quick-change acts: Nature Vol 349(6312) Feb 1991, 741-742.
- Gutfreund, Y., Flash, T., Fiorito, G., & Hochner, B. (1998). Patterns of arm muscle activation involved in octopus reaching movements: Journal of Neuroscience Vol 18(15) Aug 1998, 5976-5987.
- Hales, R. S., Crancher, P., & King, M. G. (1972). An apparatus for operant conditioning of Octopus cyaneus Gray: Behavior Research Methods & Instrumentation Vol 4(3) May 1972, 145-146.
- Hanlon, R. T., & Forsythe, J. W. (2008). Sexual cannibalism by Octopus cyanea on a Pacific coral reef: Marine and Freshwater Behaviour and Physiology Vol 41(1) Mar 2008, 19-28.
- Hartline, P. H., & Lange, D. (1977). Sinusoidal analysis of electroretinogram of squid and octopus: Journal of Neurophysiology Vol 40(1) Jan 1977, 174-187.
- Hartwick, E. B., Ambrose, R. F., & Robinson, S. M. (1984). Den utilization and the movements of tagged Octopus dofleini: Marine and Freshwater Behaviour and Physiology Vol 11(2) 1984, 95-110.
- Hartwick, E. B., Thorarinsson, G., & Tulloch, L. (1978). Methods of attack by Octopus dofleini (Wulker) on captured bivalve and gastropod prey: Marine and Freshwater Behaviour and Physiology Vol 5(3) 1978, 193-200.
- Hochner, B., Brown, E. R., Langella, M., Shomrat, T., & Fiorito, G. (2003). A Learning and Memory Area in the Octopus Brain Manifests a Vertebrate- Like Long-Term Potentiation: Journal of Neurophysiology Vol 90(5) Nov 2003, 3547-3554.
- Kayes, R. J. (1974). The daily activity pattern of Octopus vulgaris in a natural habitat: Marine and Freshwater Behaviour and Physiology Vol 2(4) Aug 1974, 337-343.
- Kobayashi, D. R. (1986). Octopus predation on hermit crabs: A test of selectivity: Marine and Freshwater Behaviour and Physiology Vol 12(2) Apr 1986, 125-131.
- Kuba, M. J., Byrne, R. A., Meisel, D. V., & Mather, J. A. (2006). Exploration and habituation in intact free moving Octopus vulgaris: International Journal of Comparative Psychology Vol 19(4) 2006, 426-438.
- Kuba, M. J., Byrne, R. A., Meisel, D. V., & Mather, J. A. (2006). When do octopuses play? Effects of repeated testing, object type, age, and food deprivation on object play in Octopus vulgaris: Journal of Comparative Psychology Vol 120(3) Aug 2006, 184-190.
- Mather, J. A. (1982). Choice and competition: Their effects on occupancy of shell homes by Octopus joubini: Marine and Freshwater Behaviour and Physiology Vol 8(4) 1982, 285-293.
- Mather, J. A. (1982). Factors affecting the spatial distribution of natural populations of Octopus joubini Robson: Animal Behaviour Vol 30(4) Nov 1982, 1166-1170.
- Mather, J. A. (1985). Behavioural interactions and activity of captive Eledone moschata: Laboratory investigations of a "social" octopus: Animal Behaviour Vol 33(4) Nov 1985, 1138-1144.
- Mather, J. A. (1992). Interactions of juvenile Octopus vulgaris with scavenging and territorial fishes: Marine and Freshwater Behaviour and Physiology Vol 19(3) Jan 1992, 175-182.
- Mather, J. A. (1998). How do octopuses use their arms? : Journal of Comparative Psychology Vol 112(3) Sep 1998, 306-316.
- Mather, J. A., & Anderson, R. C. (1993). Personalities of octopuses (Octopus rubescens): Journal of Comparative Psychology Vol 107(3) Sep 1993, 336-340.
- Mather, J. A., & Anderson, R. C. (1999). Exploration, play and habituation in octopuses (Octopus dofleini): Journal of Comparative Psychology Vol 113(3) Sep 1999, 333-338.
- Mather, J. A., Resler, S., & Cosgrove, J. (1985). Activity and movement patterns of -I Octopus defleini: Marine and Freshwater Behaviour and Physiology Vol 11(4) Jul 1985, 301-314.
- Meisel, D. V., Byrne, R. A., Kuba, M., Mather, J., Ploberger, W., & Reschenhofer, E. (2006). Contrasting activity patterns of two related octopus species, Octopus macropus and Octopus vulgaris: Journal of Comparative Psychology Vol 120(3) Aug 2006, 191-197.
- Messenger, J. B., & Sanders, G. D. (1972). Visual preference and two-cue discrimination learning in octopus: Animal Behaviour Vol 20(3) Aug 1972, 580-585.
- Michels, J., Robertson, J. D., & Young, J. Z. (1987). Can conditioned aversive tactile stimuli affect extinction of visual responses in octopus? : Marine and Freshwater Behaviour and Physiology Vol 13(1) Jun 1987, 1-11.
- Moriyama, T., & Gunji, Y.-P. (1997). Autonomous learning in maze solution by Octopus: Ethology Vol 103(6) Jun 1997, 499-513.
- Myers, C. (1992). A model of the visual attack learning system in Octopus Vulgaris: Journal of Intelligent Systems Vol 2(1-4) 1992, 225-260.
- Packard, A., & Sanders, G. D. (1971). Body patterns of Octopus vulgaris and maturation of the response to disturbance: Animal Behaviour Vol 19(4) Nov 1971, 780-790.
- Papini, M. R., & Bitterman, M. E. (1991). Appetitive conditioning in Octopus cyanea: Journal of Comparative Psychology Vol 105(2) Jun 1991, 107-114.
- Roffe, T. (1975). Spectral perception in Octopus: A behavioral study: Vision Research Vol 15(3) Mar 1975, 353-356.
- Sinn, D. L., Perrin, N. A., Mather, J. A., & Anderson, R. C. (2001). Early temperamental traits in an octopus (Octopus bimaculoides): Journal of Comparative Psychology Vol 115(4) Dec 2001, 351-364.
- Sumbre, G., Gutfreund, Y., Fiorito, G., Flash, T., & Hochner, B. (2001). Control of octopus arm extension by a peripheral motor program: Science Vol 293(5536) Sep 2001, 1845-1848.
- Suzuki, H., & Tasaki, K. (1983). Inhibitory retinal efferents from dopaminergic cells in the optic lobe of the octopus: Vision Research Vol 23(4) 1983, 451-457.
- Warren, L. R., Scheier, M. F., & Riley, D. A. (1974). Colour changes of Octopus rubescens during attacks on unconditioned and conditioned stimuli: Animal Behaviour Vol 22(1) Feb 1974, 211-219.
- Wells, M. J., O'Dor, R. K., Mangold, K., & Wells, J. (1983). Diurnal changes in activity and metabolic rate in Octopus vulgaris: Marine and Freshwater Behaviour and Physiology Vol 9(4) 1983, 275-287.
- Wells, M. J., & Young, J. Z. (1975). The subfrontal lobe and touch learning in the octopus: Brain Research Vol 92(1) 1975, 103-121.
- Wodinsky, J. (1978). Feeding behaviour of broody female Octopus vulgaris: Animal Behaviour Vol 26(3) Aug 1978, 803-813.
- Wood, J. B., & Anderson, R. C. (2004). Interspecific Evaluation of Octopus Escape Behavior: Journal of Applied Animal Welfare Science Vol 7(2) 2004, 95-106.
- Yekutieli, Y., Mitelman, R., Hochner, B., & Flash, T. (2007). Analyzing octopus movements using three-dimensional reconstruction: Journal of Neurophysiology Vol 98(3) Sep 2007, 1775-1790.
- Boal, J. G. (1993). An assessment of complex learning in octopuses: Dissertation Abstracts International.
- CephBase: Octopoda
- TONMO.COM - The Octopus News Magazine Online
- Tree of Life website: information about cephalopods along with pictures and videos
- Discussion about the plural
- An octopus' shark encounter - footage of an octopus eating a shark (also in Quicktime format)
- Camouflage in action
- Video showing an Octopus escaping through a 1 inch hole
- Bipedal Octopuses- Video, Information, Original paper
- PDF (359 KB)
- Video of walking octopuses
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