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Browsing MRC Publications by Subject "Cephalopod"
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ArticleAdaptable night camouflage by cuttlefish(University of Chicago Press, 2007-02-12) Hanlon, Roger T. ; Naud, Marie-Jose ; Forsythe, John W. ; Hall, Karina ; Watson, Anya C. ; McKechnie, JoyCephalopods are well known for their diverse, quick‐changing camouflage in a wide range of shallow habitats worldwide. However, there is no documentation that cephalopods use their diverse camouflage repertoire at night. We used a remotely operated vehicle equipped with a video camera and a red light to conduct 16 transects on the communal spawning grounds of the giant Australian cuttlefish Sepia apama situated on a temperate rock reef in southern Australia. Cuttlefish ceased sexual signaling and reproductive behavior at dusk and then settled to the bottom and quickly adapted their body patterns to produce camouflage that was tailored to different backgrounds. During the day, only 3% of cuttlefish were camouflaged on the spawning ground, but at night 86% (71 of 83 cuttlefish) were camouflaged in variations of three body pattern types: uniform (n=5), mottled (n=33), or disruptive (n=34) coloration. The implication is that nocturnal visual predators provide the selective pressure for rapid, changeable camouflage patterning tuned to different visual backgrounds at night.
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ArticleCephalopod genomics : a plan of strategies and organization(Genomic Standards Consortium, 2012-09-26) Albertin, Caroline B. ; Bonnaud, Laure ; Brown, C. Titus ; Crookes-Goodson, Wendy J. ; da Fonseca, Rute R. ; Di Cristo, Carlo ; Dilkes, Brian P. ; Edsinger-Gonzales, Eric ; Freeman, Robert J. ; Hanlon, Roger T. ; Koenig, Kristen M. ; Lindgren, Annie R. ; Martindale, Mark Q. ; Minx, Patrick ; Moroz, Leonid L. ; Nodl, Marie-Therese ; Nyholm, Spencer V. ; Ogura, Atsushi ; Pungor, Judit R. ; Rosenthal, Joshua J. C. ; Schwarz, Erich M. ; Shigeno, Shuichi ; Strugnell, Jan M. ; Wollesen, Tim ; Zhang, Guojie ; Ragsdale, Clifton W.The Cephalopod Sequencing Consortium (CephSeq Consortium) was established at a NESCent Catalysis Group Meeting, “Paths to Cephalopod Genomics- Strategies, Choices, Organization,” held in Durham, North Carolina, USA on May 24-27, 2012. Twenty-eight participants representing nine countries (Austria, Australia, China, Denmark, France, Italy, Japan, Spain and the USA) met to address the pressing need for genome sequencing of cephalopod molluscs. This group, drawn from cephalopod biologists, neuroscientists, developmental and evolutionary biologists, materials scientists, bioinformaticians and researchers active in sequencing, assembling and annotating genomes, agreed on a set of cephalopod species of particular importance for initial sequencing and developed strategies and an organization (CephSeq Consortium) to promote this sequencing. The conclusions and recommendations of this meeting are described in this White Paper.
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ArticleDramatic fighting by male cuttlefish for a female mate(University of Chicago Press, 2017-05-02) Allen, Justine J. ; Akkaynak, Derya ; Schnell, Alexandra K. ; Hanlon, Roger T.Male cuttlefish compete for females with a repertoire of visually dramatic behaviors. Laboratory experiments have explored this system in Sepia officinalis, but corroborative field data have eluded collection attempts by many researchers. While scuba diving in Turkey, we fortuitously filmed an intense sequence of consort/intruder behaviors in which the consort lost and then regained his female mate from the intruder. These agonistic bouts escalated in stages, leading to fast dramatic expression of the elaborate intense zebra display and culminating in biting and inking as the intruder male attempted a forced copulation of the female. When analyzed in the context of game theory, the patterns of fighting behavior were more consistent with mutual assessment than self-assessment of fighting ability. Additional observations of these behaviors in nature are needed to conclusively determine which models best represent conflict resolution, but our field observations agree with laboratory findings and provide a valuable perspective.
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ArticleThe lesser Pacific Striped Octopus, Octopus chierchiae: an emerging laboratory model(Frontiers Media, 2021-12-13) Grearson, Anik G. ; Dugan, Alison ; Sakmar, Taylor ; Sivitilli, Dominic M. ; Gire, David H. ; Caldwell, Roy L. ; Niell, Cristopher M. ; Dölen, Gül ; Wang, Z. Yan ; Grasse, BretCephalopods have the potential to become useful experimental models in various fields of science, particularly in neuroscience, physiology, and behavior. Their complex nervous systems, intricate color- and texture-changing body patterns, and problem-solving abilities have attracted the attention of the biological research community, while the high growth rates and short life cycles of some species render them suitable for laboratory culture. Octopus chierchiae is a small octopus native to the central Pacific coast of North America whose predictable reproduction, short time to maturity, small adult size, and ability to lay multiple egg clutches (iteroparity) make this species ideally suited to laboratory culture. Here we describe novel methods for multigenerational culture of O. chierchiae, with emphasis on enclosure designs, feeding regimes, and breeding management. O. chierchiae bred in the laboratory grow from a 3.5 mm mantle length at hatching to an adult mantle length of approximately 20–30 mm in 250–300 days, with 15 and 14% survivorship to over 400 days of age in first and second generations, respectively. O. chierchiae sexually matures at around 6 months of age and, unlike most octopus species, can lay multiple clutches of large, direct-developing eggs every ∼30–90 days. Based on these results, we propose that O. chierchiae possesses both the practical and biological features needed for a model octopus that can be cultured repeatedly to address a wide range of biological questions.
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PreprintPrimary and secondary defences of squid to cruising and ambush fish predators : variable tactics and their survival value( 2010-11-19) Staudinger, Michelle D. ; Hanlon, Roger T. ; Juanes, FrancisLongfin squid (Loligo pealeii) were exposed to two predators, bluefish (Pomatomus saltatrix) and summer flounder (Paralichthys dentatus), representing cruising and ambush foraging tactics, respectively. During 35 trials, 86 predator–prey interactions were evaluated between bluefish and squid, and in 29 trials, 92 interactions were assessed between flounder and squid. With bluefish, squid predominantly used stay tactics (68.6%, 59/86) as initial responses. The most common stay response was to drop to the bottom, while showing a disruptive body pattern, and remain motionless. In 37.0% (34/92) of interactions with flounder, squid did not detect predators camouflaging on the bottom and showed no reaction prior to being attacked. Squid that did react, used flee tactics more often as initial responses (43.5%, 40/92), including flight with or without inking. When all defence behaviours were considered concurrently, flight was identified as the strongest predictor of squid survival during interactions with each predator. Squid that used flight at any time during an attack sequence had high probabilities of survival with bluefish (65%, 20/31) and flounder (51%, 18/35). The most important deimatic/protean behaviour used by squid was inking. Inking caused bluefish to startle (deimatic) and abandon attacks (probability of survival = 61%, 11/18) and caused flounder to misdirect (protean) attacks towards ink plumes rather than towards squid (probability of survival = 56%, 14/25). These are the first published laboratory experiments to evaluate the survival value of antipredator behaviours in a cephalopod. Results demonstrate that squid vary their defence tactics in response to different predators and that the effectiveness of antipredator behaviours is contingent upon the behavioural characteristics of the predator encountered.