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      Sex-biased predation and the risky mate-locating behaviour of male tick-tock cicadas (Homoptera: Cicadidae)

      Animal Behaviour
      Elsevier BV

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          Sexual difference theory: mormon crickets show role reversal in mate choice.

          D Gwynne (1981)
          Male Mormon crickets produce a large spermatophore that the female eats. Spermatophore proteins are important to female reproduction, and females compete for access to singing males. Males reject most receptive females as mates, and those accepted are more fecund than rejected individuals. This role reversal in courtship is in contrast to the behavior of the sexes in katydid species in which the males produce small spermatophores.
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            Male crickets feed females to ensure complete sperm transfer.

            The spermatophore transferred by the male decorated cricket Gryllodes supplicans to the female during copulation includes a large gelatinous portion (spermatophylax), which the female removes and feeds on immediately after mating. Females usually removed and ate the smaller sperm-containing portion (ampulla) within 1 to 7 minutes after fully consuming or losing the spermatophylax. Complete sperm transfer requires that the ampulla remain attached for a minimum of 50 minutes; this corresponds to the average time at which females actually removed ampullae, 52.0 +/- 2.2 minutes after mating. These results indicate that nuptial feeding of the female cricket functions to deter females from removing the sperm ampulla before sperm transfer is complete.
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              Gecko phonotaxis to cricket calling song: A case of satellite predation

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                Author and article information

                Journal
                Animal Behaviour
                Animal Behaviour
                Elsevier BV
                00033472
                April 1987
                April 1987
                : 35
                : 2
                : 571-576
                Article
                10.1016/S0003-3472(87)80283-X
                5c598405-13a1-4439-9a59-4edc937bbdb0
                © 1987

                http://www.elsevier.com/tdm/userlicense/1.0/

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