Grimalditeuthis
Grimalditeuthis bonplandi
Richard E. Young and Clyde F. E. RoperIntroduction
Grimalditeuthis bonplandi is very gelatinous and contains vesiculate tissue in the head, arms and mantle. It is generally Chiroteuthis-like in appearance (long neck, body and fin shape) but is distinguished by subequal arms and fusion of each funnel-mantle locking apparatus. Only scattered chromatophores are present, and the eyes are small. This species is infrequently captured but seems to have a world-wide distribution in tropical to temperate seas.
Diagnosis
A chiroteuthid ...
- without suckers on clubs.
- with funnel fused to mantle at each funnel-mantle lock.
- without photophores except on arm tips in mature (?) females.
Characteristics
- Arms
- Arms approximately subequal in length, gelatinous.
- Sucker base with three conical papillae (unique character).
- Protective membranes absent.
- Tentacles
- Club divided into two portions by symmetrical protective membranes.
- Suckers absent from clubs. Click on an image to view larger version & data in a new window
Figure. Tentacle-clubs of G. bomplandi. A - Aboral view. B - Oral view. a single intact tentacle was found on a specimen taken from the stomach of the fish Alepisaurus ferox (courtesy of Lourdes Burgess). The tentacle club lacked suckers and showed no indication that suckers or sucker stalks were ever present as the skin was intact. Drawings by A. D. Hart.
- Head
- Olfactory organ located lateral to base of funnel (i.e., immediately anterior to collar at posterior end of neck).
- Beaks with distinctive appearance.
- Olfactory organ located lateral to base of funnel (i.e., immediately anterior to collar at posterior end of neck).
- Funnel
- Funnel valve present.
- Funnel fused to mantle at each funnel-mantle locking-apparatus (head not fused to mantle in nuchal region).
- Photophores
- Absent accept at the arm tips of mature (?) females (See "More details ...").
- Absent accept at the arm tips of mature (?) females (See "More details ...").
- Tail
- Tail retained in adults with two fin-like "floatation devices" (= secondary fins) arise from tail.
Comments
More details of the description can be found here.The function of the suckerless club is unknown. Tentacle stalks are very thin, fragile and almost always broken off in capture.
This species also has a very characteristic pattern of chromatophores on the head. A line of chromatophores passes across the ventral surface of the head between the anterior ends of eyes; another line runs along the neck from each olfactory papilla anteriorly to each eye, then anterior to each eye along the brachial pillar, terminating at the base of the arms.
Nomenclature
Joubin (1898) described a second species, G. richardi based on the presence of photophores on the tips of the arms. Pfeffer (1912) synonomized the two and this was supported by Young (1972) and Nesis (1982).
Life History
The doratopsis was first described by Chun (1910) as Doratopsis sagitta. A growth series of the paralarvae was described by Young (1991), and can be found below. The early doratopsis stage is similar to that of other species in the family. The older doratopsis shows many of the features of the subadult including the distinctive chromatophore pattern and the small eyes.
- At sizes larger than 9 mm ML Grimalditeuthis doratopsis paralarvae are easily identified by:
- Small eye size.
- Position of the olfactory papillae opposite the base of the funnel.
- Distinctive chromatophore pattern on the head (same as subadult pattern).
- Separation of optic lobes from brain.
- Anterior position of the superior buccal and brachial lobes.
- At sizes smaller than 9 mm paralarvae are identified by a combination of:
- A long brachial pillar with a centrally located esophagus.
- Number of chromatophores on the funnel shoulders and the ventral head posterior to the eyes.
- Just slightly elongate eye-shape.
- Shape of the vesiculate area on the posterior end of the mantle (nearly flat anteriorly).
Distribution
Vertical distribution
A small number of captures off Hawaii (Young 1978) included three small squid from the upper 350 m that probably had not descended from the shallow paralarval habitat and five squid from depths greater than 700 m.
Geographical distribution
The type locality is 29° N and 39° W in the North Atlantic. It is known from the tropical and subtropical North Atlantic and the tropical and temperate North Pacific (Nesis, 1982).
References
Joubin, L. 1898. Observations sur divers Cephaloppodes. Quatrieme note: Grimalditeuthis Richardi Joubin 1898. Bulletin de la Societe Zoologique de France, 23: 101-113.
Pfeffer, G. 1912. Die Cephalopoden der Plankton-Expedition. Ergebniss der Plankton-Expedition der Humboldt-Stiftung. 2: 1-815.
Verany, J. B. 1839. Memoire sur six novelles especes de Cephalopodes trouvees dans la Mediterranee a Nice. Memoire della Resle Accademia della Science de Torino, series 2, 1: 91-98
Young, R. E. 1972. The systematics and areal distribution of pelagic cephalopods from the seas off Southern California. Smithson. Contr. Zool., 97: 1-159.
Young, R. E. 1978. Vertical distribution and photosensitive vesicles of pelagic cephalopods from Hawaiian waters. Fish. Bull., 76: 583-615.
Young, R. E. 1991. Chiroteuthid and related paralarvae from Hawaiian waters. Bull. Mar. Sci. 49: 162-185.
About This Page
Richard E. Young
University of Hawaii, Honolulu, HI, USA
Smithsonian Institution, Washington, D. C., USA
Page copyright © 1999 Richard E. Young and
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- Content changed 05 September 2008
Citing this page:
Young, Richard E. and Roper, Clyde F. E. 2008. Grimalditeuthis http://tolweb.org/Grimalditeuthis_bonplandi/19463/2008.09.05 in The Tree of Life Web Project, http://tolweb.org/
. Grimalditeuthis bonplandi . Version 05 September 2008 (under construction).