Distastefulness as a defense mechanism in Aplysia brasiliana (Mollusca: Gastropoda)

The biochemical literature on the toxicity of various species of Aplysia is reviewed to indicate that Aplysia are probably not toxic to predators under natural conditions. The possibility that Aplysia avoid prrdation by being distasteful is examined by offering various portions of Aplysia brasiliana and pieces of fish to sea gulls. Gulls are shown to find all parts of Aplysia more distasteful than fish, even fish soaked in a mixture of Aplysia blood, mucus, and ink. Ink gland, gill, and epidermal portions are shown to be significantly more distasteful than other portions, even the midgut and opaline glands, sites of compounds which can be toxic when injected. Distastefulness as a mechanism for avoiding predation and the possible function of the ink gland are discussed in light of these findings and current literature.

[1]  Scheuer Pj,et al.  Recent developments in the chemistry of marine toxins. , 1975 .

[2]  I Kupfermann,et al.  Behavior patterns of Aplysia californica in its natural environment. , 1974, Behavioral biology.

[3]  P. Scheuer,et al.  Aplysiatoxin and debromoaplysiatoxin, constituents of the marine mollusk Stylocheilus longicauda (Quoy and Gaimard, 1824). , 1974, Journal of the American Chemical Society.

[4]  J. Fayós,et al.  (3R,4S,7S)-trans, trans-3,7-Dimethyl-1,8,8-tribromo-3,4,7-trichloro-1,5-octadiene, a novel monoterpene from the sea hare, Aplysia californica , 1973 .

[5]  M. Watson Midgut gland toxins of Hawaiian sea hares. I. Isolation and preliminary toxicological observations. , 1973, Toxicon : official journal of the International Society on Toxinology.

[6]  M. Rayner,et al.  Midgut gland toxins of Hawaiian sea hares. II. A preliminary pharmacological study. , 1973, Toxicon : official journal of the International Society on Toxinology.

[7]  D. Faulkner,et al.  7-chloro-3,7-dimethyl-1,4,6-tribromo-1-octen-3-ol, a novel monoterpene alcohol from , 1973 .

[8]  Y. Hirata,et al.  A Naturally-occurring Bromo-compound, Aplysin-20 from Aplysia kurodai , 1971 .

[9]  D. L. Fox,et al.  Bile pigment metabolism in the sea-hare Aplysia , 1969 .

[10]  Minoru Suzuki,et al.  Isolation of Aplysin, Debromoaplysin, and Aplysinol from Laurencia Okamurai Yamada , 1969 .

[11]  M. Toda,et al.  The synthesis of (±)-aplysin and (±)-debromoaplysin , 1968 .

[12]  B. Halstead,et al.  POISONOUS AND VENOMOUS MARINE ANIMALS OF THE WORLD: REVIEW OF MONOGRAPH , 1969 .

[13]  T. Masamune,et al.  A new sesquiterpene hydrocarbon from , 1965 .

[14]  E. Tobach,et al.  Preliminary observations of the inking behavior of Aplysia lVarriar , 1965 .

[15]  J. Phillips,et al.  An experiment in undergraduate teaching and research in the biological sciences [marine biology] , 1964 .

[16]  Y. Hirata,et al.  Structures of aplysin and aplysinol, naturally occurring bromo-compounds , 1963 .

[17]  B. E. Tilton,et al.  Predation on the California Sea Hare, Aplysia californica Cooper, by the Solitary Great Green Sea Anemone, Anthopleura xanthogrammica (Brandt), and the Effect of Sea Hare Toxin and Acetylcholine on Anemone Muscle , 1962 .

[18]  L. R. Winkler Preliminary Tests of the Toxin Extracted from California Sea Hares of the Genus Aplysia , 1961 .

[19]  T. E. Thompson Defensive acid-secretion in marine gastropods , 1960, Journal of the Marine Biological Association of the United Kingdom.

[20]  T. E. Thompson Defensive adaptations in opisthobranchs , 1960, Journal of the Marine Biological Association of the United Kingdom.

[21]  C. Munn The pigments of Aplysia Punctata , 1899, The Journal of physiology.

[22]  H. N. Moseley Memoirs: On the Colouring Matters of Various Animals, and especially of Deep-sea Forms dredged by H.M.S. Challenger , 1877 .