Octopods, squids, cuttlefishes and their relativesRichard E. Young, Michael Vecchione, and Katharina M. Mangold (1922-2003)
The Coleoidea contains all living cephalopods except for species of pearly nautilus.
This tree diagram shows the relationships between several groups of organisms.
The root of the current tree connects the organisms featured in this tree to their containing group and the rest of the Tree of Life. The basal branching point in the tree represents the ancestor of the other groups in the tree. This ancestor diversified over time into several descendent subgroups, which are represented as internal nodes and terminal taxa to the right.
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Most fossil neocoleoids that are often considered as teuthoids are placed here under Octopodiformes.
Mesozoic Spirulida of the Decapodiformes are placed under Spirulida.
The Coleoidea contains two subdivisions. One, the Belemnoidea, had members that were common inhabitants of neritic waters during the Cretaceous but became extinct and the end of this Period.
The other subdivision, the Neocoleoidea, contains two extant groups: the Octopodiformes (octopods and vampire squid) and the Decapodiformes (squids and cuttlefishes). In addition, a variety of fossil groups exist that may fall into either of these two groups of neocoleoids. The extant coleoids occupy all major habitats in the ocean from intertidal to great depths (deepest record is 7279m, Aldred et al., 1983; Voss, 1988,p. 266) and from south to north polar regions. Although some loliginid squids and some sepiolids can tolerate reduced salinity, no cephalopod occurs in fresh water. In many regions of the oceans, coleoids are dominant members of the ecosystem and are often targets of major fisheries.
Coleoids generally use mantle-generated jet propulsion to obtain high swimming speeds. This is an effective but energetically expensive means of locomotion (Webber and O'Dor, 1985) and, as a result, some groups utilize the fins as the primary locomotor organ. This is especially common in deep-sea species (e.g., cirrate octopods, octopoteuthid squid, magnapinnid squid) where, in dark waters, the value of speed is reduced.
When cephalopods first evolved, the primary feature that separated them from other molluscs was a shell with buoyancy chambers. This allowed cephalopods to invade the pelagic realm where predators and competitors were few. When the shell became internal in coleoids the bouyancy chambers were retained in belemnoids. In most present day neocoleoids, the buoyant shell has been abandoned (it is retained in Spirula and the Sepiidae) and many squids and octopods are negatively buoyant. While this is not a problem for those octopods that are benthic, negatively buoyant squids, however, must swim constantly to stay afloat. Some squids and pelagic octopods, however, have gained near-neutral buoyancy via the retention of light ions (especially ammonium in place of sodium) and the reduction of heavy tissues (Clarke, et al., 1979). This type of neutral buoyancy is found in many deep-sea species since reduction of muscular and cartilagenous tissues can be tolerated in this habitat. In a few cases oil provides buoyancy (Bathyteuthidae) and in one case (Ocythoidae) a true swimbladder has evolved (Packard and Wurtz, 1994).
Coleoid arms are unique grasping structures that possess a variety of different types of suckers and hooks. The arms and suckers are also provided with a variety of sensory organs that can be a primary means of investigating the immediate environment. This is especially true of the octopods where the arms can hunt for unseen prey under rocks. Prey are seized and passed to the mouth then cut into pieces by sharp beaks and swallowed. Because of the circumesophageal organization of the molluscan central nervous system and its elaboration into a complex brain in cephalopods, the cephalopod esophagus passes through the center of the brain; this arrangement limits the maximum size of particles that can be swallowed.
Survival in the sea depends not only on obtaining food but also on avoiding predators. Although preyed upon by many vertebrates (especially marine mammals) and other animals, coleoids excel at camouflage and deception (see Hanlon and Messenger, 1996). They easily exceed all other animals in their ability to change color quickly through the use of chromatophoric organs (chromatophores) and various types of reflectors. The chromatophores contain muscles under nervous control; quick muscle contraction produces rapid color changes that immediately changes the appearance of the animal. This camouflage, combined with their ability to secrete clouds or globs of ink, and the ability of many to alter their skin texture and arm postures, provides them exceptional concealment abilities.
Another, perhaps surprising feature of coleoids, since many species reach a large size, is their short life span. Most species grow rapidly and live for one year or less. Reasons for this are not well understood. However, this is part of a life-history strategy that seems designed for rapid increase in population size. One result of this is that cephalopod fisheries typically fluctuate wildly in annual catch rates.
- Shell located internally.
- Muscular mantle for propulsion and respiration.
- Brachial crown consisting of ten arms. Click on an image to view larger version & data in a new window
- Fins present*
- Chromatophores present*
- Ink sac present.
- Eyes with lenses.
* presence not established in Belemnoidea.
Many of these characters have been secondarily lost in various taxa.
Arm pairs are counted from dorsal to ventral as indicated in the illustration above. However, the numbering of arms in taxonomic descriptions leads to some ambiguity. In the Decapodiformes, the fourth of five pairs of arms has been modified as tentacles, leaving four pairs of functional arms. As a result, the ventral arms are the true fifth pair but functionally are the fourth pair. Similarly, the second pair of arms is modified in vampyroteuthids and lost in octopods causing a difference between true (i.e., homologous) and functional arm-pair numbering. True arm-pair numbering is used in the above illustration while functional numbering is used in descriptions of taxa.
General consensus on the names of higher taxonomic catagories in the Coleoidea has not been achieved (eg, see Berthold and Engeser, 1987; Clarke, 1988; Doyle, et al., 1994; Haas, 2002).
Extant coleoids form a monophyletic group, the Neocoleoidea, as evidenced by the uniform presence of suckers. Their sister group, the Belemnoidea, is characterized by the presence of hooks that are derived, perhaps, from muscular papillae, the homologues of trabeculae or cirri that lie lateral to the suckers in living coleoids (e.g. Engeser and Bandel, 1988, see also Haas, 1989).
The Decapodiformes is supported by only a single morphological character that has been demonstrated to be apomorphic (i.e. derived): the modification of the fourth pair of arms as tentacles (Young and Vecchione, 1996). The monophyly, however, is supported by molecular cladistic studies (Bonnaud et al. 1997; Carlini and Graves, 1999). The problem with morphology, however, is not due to a lack of shared character states among decapods but instead results from our inability to polarize these states. The outgroup on which most polarity decisions are based is the Nautiloidea. Unfortunately, this group is morphologically very different from coleoids and many characters are not applicable to both groups.
Young and Vecchione (1996, 2002) found five unambiguous character states that supported the monophyly of the Octopodiformes:
- Presence of an outer statocyst capsule.
- Superior buccal lobes adjacent (fused at edges) or fused to posterior buccal lobes of the brain.
- Arms II modified as filaments. (This assumes an "ordered" evolutionary relationship of the character states: arms II unmodified - arms II modified - arms II absent.)
- Primary gill lamellae possess a partial or complete median septum.
- Secondary gill lamellae possess a partial or complete median septum.
An evolutionary study by Hass (2002) also placed the Vampyromorpha and Octopoda together as a monophyletic group on the basis of a combination of characters four and five above (he independently recognized these characters but defined them slightly differently). Molecular studies support the monophyly of this group (Carlini and Graves, 1999) or give it equivocal support (Bonnaud et al., 1997).
Aldred, R. G., M. Nixon and J. Z. Young. 1983. Cirrothauma murrayi Chun, a finned octopod. Phil. Trans. Roy. Soc. Lond. 301: 1-54.
Berthold, T. and T. Engeser. 1987. Phylogenetic analysis and systematization of the Cephalopoda (Mollusca). Verh. Naturwiss. Ver. Hamburg 29: 187-220.
Bonnaud, L., R. Boucher-Rodoni and M. Monnerot. 1997. Phylogeny of cephalopods infered from mitochondrial DNA sequences. Mol. Phylog. Evol. 7: 44-54.
Carlini, D. B. and J. E. Graves. 1999. Phylogenetic analysis of cytochrome c oxidase I sequences to determine higher-level relationships within the coleoid cephalopods. Bull. Mar. Sci., 64: 57-76.
Clarke, M. R. 1988. Evolution of recent cephalopods -- A brief review. P. 331-313. In: Clarke, M. R. and E. R. Trueman (Eds.). The Mollusca. Vol. 12. Paleontology and Neontology of Cephalopods. Academic Press, New York. 355pp.
Clarke, M., E. Denton and J. Gilpin-Brown. 1979. On the use of ammonium for buoyancy in squids. J. Mar. Biol. Ass. U. K., 59: 259-276.
Doyle, P., D. T. Donovan and M. Nixon. 1994. Phylogeny and systematics of the Coleoidea. Univ. Kansas Paleont. Contrib. No. 5: 1-15.
Engeser, T. and K. Bandel. 1988. Phylogenetic classification of coleoid cephalopods. In: Wiedmann, J. and Kullmann, J. (Eds.), Cephalopods. Present and past. p105-115. Stuttgart.
Haas, W. 1989. Suckers and arm hooks in Coleoidea (Cephalopoda, Mollusca) and their bearing for phylogenetic systematics. Abh. Naturwiss. Ver. Hamburg, 28: 165-185.
Haas, W. 2002. The evolutionary history of the eight-armed Coleoidea. Abh. Geol. B.-A, 57: 341-351.
Hanlon, R. T. and J. B. Messenger. 1996. Cephalopod Behaviour. New York; Cambridge University Press: 232 pp.
Packard, A. and M. Wurtz. 1994. An octopus, Ocythoe, with a swimbladder and triple jets. Phil. Trans. R. Soc. Lond. B 344: 261-275.
Vecchione, M., R. E. Young, D. T. Donovan and P. G. Rodhouse. 1999. Reevaluation of coleoid cephalopod relationships based on modified arms in the Jurassic coleoid Mastigophora. Lethaia, 32: In press.
Voss, G. L. 1988. Evolution and phylogenetic relationships of deep-sea octopods (Cirrata and Incirrata). P. 253-276. In: Clarke, M. R. and E. R. Trueman (Eds.). The Mollusca. Vol. 12. Paleontology and Neontology of Cephalopods. Academic Press, New York. 355pp.
Webber, D. M. and R. K. O'Dor. 1985. Respiration and swimming performance of short-finned squid (Illex illecebrosus). NAFO Sci. Coun. Studies, 9: 133-138.
Young, R. E. and M. Vecchione. 1996. Analysis of morphology to determine primary sister taxon relationships within coleoid cephalopods. Bull. Amer. Malac. Union 12:91-112.
Young, R. E. and M. Vecchione. (2002). Evolution of the gills in the Octopodiformes. Bull. Mar. Sci., 71:1003-1018.
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Young, Richard E., Michael Vecchione, and Katharina M. Mangold (1922-2003). 2012. Coleoidea http://tolweb.org/Coleoidea/19400/2012.07.04 in The Tree of Life Web Project, http://tolweb.org/. Octopods, squids, cuttlefishes and their relatives. Version 04 July 2012 (under construction).