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Cranchia scabra

Described by Leach, 1817

Page authors: Aaron Boyd Evans, Richard E. Young, Katharina M. Mangold

Cranchia scabra
© Danté Fenolio

The genus Cranchia (Leach, 1817) contains a single known species, C. scabra. The mantle is covered in multi-pointed, stellate tubercles and the surface, two cartilaginous lines of tubercles originate from the ventral mantle fusion points on either side of the funnel forming a “V” shape.  Other distinguishing features include circular fins and circular ocular photophores on each eye (a characteristic shared among the Cranchiinae). 

Quick Facts: When disturbed, the squid often pulls its head and arms into the mantle cavity and folds its fins tightly against the mantle to form a turgid ball. The tubercules, presumably, provide some type of protection but it is unclear what predators are affected and how. In addition, the squid may ink into the mantle cavity, making the ball opaque - this was believed to be an aberrant behavior due to the stress and confinement of shipboard aquaria until the same inking behavior was seen in cranchiids from submersibles (Hunt, 1996). The function of this behavior remains unknown.

Tentacles

  • Suckers in a transverse row on club manus of equal size.
  • Diagonally set pairs of suckers and pads on distal 2/3 of tentacular stalk

Arms

  • Arm III with slight aboral keel.
  • Arms with 40-70 spherical suckers
  • Sucker teeth are generally angular but can be more rounded in basal pairs of suckers.
  • Mature females with darkened, brachial organs on all arms, those on arm III enlarged. 

Adult Female Cranchia

Figure Ventral view of a maturing (?) but damaged female C. scabra, Gulf of Mexico, 150 mm ML, showing the red-pigmented photophores at the tips of the arms. Photograph by M. Vecchione.

Head

  • Eyes sessile in paralarvae (this is uncommon in Cranchiidae and can help with paralarval identification).

Photophores

  • Fourteen oval photophores on each eye (ventral-proximal series of 8 photophores, ventral-distal series of 4 photophores near lens and dorsal series of two photophores near lens).

Ventral view of most ocular photophores of C. scabra. The dorsal series of photophores is not visible. Photograph by M. Vecchione.

Figure Ventral view of most ocular photophores of C. scabra. The dorsal series of photophores is not visible. Photograph by M. Vecchione.

Mantle

  • Mantle is rotund and covered with cartilaginous tubercles bearing 3-5 sharp cusps.

Cranchia Tubercles

Figure. Lateral view of part of the mantle and head of a 30 mm ML C. scabra showing tubercles. Photograph by R. Young.

Fins

  • Each fin is circular to oval in shape with free posterior lobes.  Tubercles are present on dorsal surface of the fins, radiating outward from the gladial midline.

 

Cranchia scabra is the only known member of the genus Cranchia

Cranchia is found circumglobally at both tropical and sub-tropical latitudes (43°N to 43°S).  The species is believed to exhibit ontogenetic descent (living in epipelagic waters in infancy and descending deeper into the water column upon maturation).  The deepest recorded C. scabra was discovered at 2000 meters depth (Jereb & Roper, 2010).

Cranchia is one of the few cranchiid genera to undergo relatively minimal morphological development throughout ontogeny.  As mentioned previously, paralarvae are most often recorded between 500-0m depth while adults are frequently found at lower depths.  Like other cranchiids, the eyes will expand in size during maturation, but unlike many other Cranchiidae are not stalked in younger life stages.  Tubercles become more complex throughout development and cover greater areas of the outer mantle and fins as the animal develops.

Upon reaching maturation, secondary sexual characteristics develop.  In females, brachial end organs form on all arms, with those on arms III being longer than the others (Evans, 2018).  Mature males develop a hectocotylus on right Arm IV, with minor modifications on Arm III (Voss, 1980).   

Cscabra Paralarvae 1Cscabra Paralarvae 2

Figure Paralarval C. scabraLeft - Ventral and dorsal views, 4.7 mm ML, Hawaiian waters. Chromatophores were faint and pattern may not be complete; at slightly larger sizes the chromatophores cover the entire mantle. Drawings by R. Young.  Right - Ventral view, 8 mm ML, showing tubercules, not chromatophores. Drawing from Voss, 1980, p. 377, printed with the permission of the Bulletin of Marine Science. Scale bar is 1 mm.

 

Voss (1983) found strong phylogenetic support for character distinctions between the sub-families Cranchiinae and Taoniinae and indicated that Cranchia and Liocranchia likely had the most primitive physical characters.  Evans (2018) found Leachia to be the most basal of the Cranchiinae, but molecular data for the Cranchiinae was limited in his research.  More genetic assessments are needed to better understand phylogenetic relationships between the Cranchiinae. 

Cranchia scabra is thought to be a circumglobal species.  No known ecological or morphological differences are known between geographically separate groups. 

Cranchia scabra Leach, 1817: 140; Leach, 1818: 13, Pl. 18; Owen 1836: 103–108, Pl. XXI fig. 1–5; Férussac & d’Orbigny, 1834: 222–224, Pl. I fig. 1; d’Orbigny, 1845: 239–240, Pl. 8; Steenstrup, 1861: 28–31; Chun, 1910: 257–262, Pl. XLVIII fig. 1–2, Pl. XLIX, L, LX fig. 1–6; Pfeffer, 1912: 678–689; Robson, 1924: 10; Young, 1972: 78–80; Imber, 1978: 448–449, fig. 1a; Voss, Stephen, & Dong, 1992: 188–189, fig. 217; Reid, 2016: 82–83.

Loligo cranchii d’Blainville, 1823: 123.

Octopus (Philonexis) eylais d’Orbigny, 1834: 20, Pl. I fig. 8–14.

Cranchia hispida Pfeffer, 1884: 27, fig. 37.

Cranchia tenuitententaculata Pfeffer, 1884: 26–27, fig. 36.

Cranchia scabra hispida Pfeffer, 1912: 690–691, Pl. 48 fig. 27.

Cranchia scabra tenuitentaculata Pfeffer, 1912: 689–690, Pl. 48 fig. 28.

Evans, A.B. 2018. A Systematic Review of the Squid Family Cranchiidae (Cephalopoda: Oegopsida) in the Pacific Ocean. [PhD Thesis, Auckland University of Technology]. https://openrepository.aut.ac.nz/items/0eb9f5c7-e06d-4513-80d3-18b87774a08d

Hunt, J. 1996. The behavior and ecology of midwater cephalopods from Monterey Bay: Submersible and laboratory observations (Publication No. 9616414) [Doctoral Dissertation, University of California, Los Angeles]. ProQuest Dissertations and Theses Global.

Jereb, P. & Roper, C.F.E. (eds) (2010). Cephalopods of the world. An annotated and illustrated catalogue of cephalopod species known to date. Volume 2. Myopsid and Oegopsid Squids. FAO Species Catalogue for Fishery Purposes, No. 4 (2): 148-178.  

Leach W.E. 1817. Synopsis of the orders, families and genera of the class Cephalopoda. The Zoological Miscellany; being descriptions of new or interesting animals3(30): 137-141.

Roper, C.F.E. & Lu C.C. 1990. Comparative morphology and function of dermal structures in oceanic squids (Cephalopoda). Smithsonian Contributions to Zoology, 493: 1-40.

Voss, N.A. 1980. A generic revision of the Cranchiidae (Cephalopoda; Oegopsida). Bulletin of Marine Science, 30(2): 365-412.

Voss, N.A. & Voss, R.S. 1983. Phylogenetic relationships in the cephalopod family Cranchiidae (Oegopsida). Malacologia, 23(2): 397-426.

Young, R.E. 1972. The systematics and areal distribution of pelagic cephalopods from the seas off Southern California. Smithsonian Contributions to Zoology, 97: 1-159.

Taxonomy

Superorder
Decapodiformes
Superfamily
Cranchioidea
Cranchia scabra - CEPH REF | CephRef