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  • 1
    Publication Date: 2020-06-19
    Description: Over 1200 squids were captured by night lighting, trawling, or seining in the northern Gulf of Mexico for laboratory maintenance. Two types of recirculating sea water systems were designed and evaluated: a 2 m circular tank (1500 liter capacity) and a 10 m long raceway (10,000 liters). Mean laboratory survival was: Loligo plei (12 to 252 mm mantle length, ML) 11 days, maximum 84 days; Loligo pealei (109 to 285 mm ML) 28 days, maximum 71 days; Lolliguncula brevis (27 to 99 mm ML) 19 days, maximum 125 days. Smaller squids showed significantly poorer survival than larger ones. All squids fed well on a variety of live estuarine fishes and shrimps. Growth rates depended upon stage of maturity. The highest rates were Loligo plei 59 mm/month (23.8 g/mo), Loligo pealei 77 mm/mo (67.3 g/mo), and Lolliguncula brevis 31 mm/mo (17.2 g/mo). General aspects of behavior and body patterning were species-specific and were useful indices of the squids' condition. Key factors for laboratory survival were (1) prevention of skin damage, (2) tank systems with sufficiently large horizontal dimensions, (3) high quality water, (4) ample food supply, (5) no crowding, (6) maintaining squids of similar size to reduce aggression and cannibalism, and (7) segregating sexes to reduce aggression associated with courtship, mating, and egg laying.
    Type: Article , PeerReviewed
    Format: text
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  • 2
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    University of Chicago Press
    In:  The American Naturalist, 129 (2). pp. 312-317.
    Publication Date: 2020-05-13
    Type: Article , PeerReviewed
    Format: text
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  • 3
    Publication Date: 2022-05-25
    Description: Author Posting. © University of Chicago Press, 2007. This article is posted here by permission of University of Chicago Press for personal use, not for redistribution. The definitive version was published in American Naturalist 169 (2007): 543–551, doi:10.1086/512106.
    Description: Cephalopods 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.
    Description: This work was made possible by grant 7456-03 from the National Geographic Society Committee on Research and Exploration and support from the Sholley Foundation.
    Keywords: Crypsis ; Concealment ; Disruptive coloration ; Coincident disruptive coloration ; Cephalopod ; Sepia apama
    Repository Name: Woods Hole Open Access Server
    Type: Article
    Format: application/pdf
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  • 4
    Publication Date: 2022-05-25
    Description: Author Posting. © University of Chicago Press, 2017. This article is posted here by permission of University of Chicago Press for personal use, not for redistribution. The definitive version was published in The American Naturalist 190 (2017): 144-151, doi:10.1086/692009.
    Description: 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.
    Description: J.J.A. was supported by a National Defense Science and Engineering Graduate Fellowship and a National Science Foundation Graduate Research Fellowship; A.K.S. was supported by a postdoctoral study grant from the Fyssen Foundation; R.T.H. was funded partly by the Sholley Foundation and supported by Office of Naval Research grant N0001406-1-0202.
    Description: 2018-05-02
    Keywords: Sepia officinalis ; Agonistic ; Cephalopod ; Behavior ; Sexual selection ; Evolutionary game theory
    Repository Name: Woods Hole Open Access Server
    Type: Article
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