51. Ianora A, Miralto A (2010) Toxigenic effects of diatoms on grazers, phytoplankton and other
microbes: a review. Ecotoxicology 19: 493–511
52. Adiyodi G, Adiyodi G (1970) Endocrine control of reproduction in decapod crustacea. Biol Rev
45:121–165
53. Zupo V (1994) Strategies of sexual inversion in Hippolyte inermis Leach (Crustacea,
Decapoda) from a Mediterranean seagrass meadow. J Exp Mar Biol Ecol 178:131–145
54. Zupo V (2000) Effect of microalgal food on the sex reversal of Hippolyte inermis (Crustacea:
Decapoda). Mar Ecol Prog Ser 201:251–259
55. d’Udekem d’Acoz C (1996) The genus Hippolyte Leach, 1814 (Crustacea: Decapoda: Caridea:
Hippolytidae) in the East Atlantic Ocean and the Mediterranean Sea, with a checklist of all
species in the genus. Zool Verhand 303:1–133
56. Zupo V, Messina P, Buttino I, Sagi A, Avila C, Nappo M, Bastida J, Codina C, Zupo S (2007)
Do benthic and planktonic diatoms produce equivalent effects in crustaceans? Mar Freshw
Behav Physiol 40:1–13. https://doi.org/10.1080/10236240701592930
57. Buia MC, Gambi MC, Zupo V (2000) Structure and functioning of Mediterranean seagrass
ecosystems: an overview. Biol Mar Medit 7(2):167–190
58. Charniaux-Cotton H (1967) Endocrinologie et génétique de la différenciation sexuelle chez
les invertébrés. C R Seances Soc Biol 16:6–9
59. Levy T, Manor R, Tamone SL, Aflalo ED, Sagi A (2017) Sexual differentiation during the life
history of a protandric shrimp. Integr Comp Biol 57(1):E327–E327
60. Bortolini JL, Bauet RT (2017) Persistence of reduced androgenic glands after protandric sex
change is a possible basis for simultaneous hermaphroditism in the marine shrimp Lysmata
wurdemanni. Integr Comp Biol 57(1):E208
61. Zupo V, Messina P, Carcaterra A, Aflalo ED, Sagi A (2008) Experimental evidence of a sex
reversal process in the shrimp Hippolyte inermis. Invertebr Reprod Dev 52(1–2):93–100
62. Reverberi G (1950) La situazione sessuale di Hippolyte viridis e le condizioni che la reggono.
Boll Zoologico 4:91–94
63. Zupo V (2001) Influence of diet on sex differentiation of Hippolyte inermis Leach (Decapoda:
Natantia) in the field. Hydrobiologia 449:131–140
64. Cobos V, Diaz V, Raso G, Enrique J, Manjon-Cabeza ME (2005) Insights on the female
reproductive system in Hippolyte inermis (Decapoda, Caridea): is this species really hermaphroditic? Invertebr Biol 124:310–320
65. Charnov EL, Los-den Hartogh RL, Jones WT, van den Assem J (1981) Sex ratio evolution in
a variable environment. Nature 289:27–33
66. Charnov EL (1982) The theory of sex allocation. Princeton University Press, Princeton, NJ,
USA
67. Zupo V, Jüttner F, Maibam C, Butera E, Blom JF (2014) Apoptogenic metabolites in fractions
of the benthic diatom Cocconeis scutellum parva. Mar Drugs 12:547–567. https://doi.org/
10.3390/md12010547
68. Juettner F, Messina P, Patalano C et al (2010) Odour compounds of the diatom Cocconeis
scutellum: effects on benthic herbivores living on Posidonia oceanica. Mar Ecol Prog Ser
400:63–73
7 Co-evolution of the Shrimp Hippolyte inermis and the Diatoms Cocconeis. . .
147
microbes: a review. Ecotoxicology 19: 493–511
52. Adiyodi G, Adiyodi G (1970) Endocrine control of reproduction in decapod crustacea. Biol Rev
45:121–165
53. Zupo V (1994) Strategies of sexual inversion in Hippolyte inermis Leach (Crustacea,
Decapoda) from a Mediterranean seagrass meadow. J Exp Mar Biol Ecol 178:131–145
54. Zupo V (2000) Effect of microalgal food on the sex reversal of Hippolyte inermis (Crustacea:
Decapoda). Mar Ecol Prog Ser 201:251–259
55. d’Udekem d’Acoz C (1996) The genus Hippolyte Leach, 1814 (Crustacea: Decapoda: Caridea:
Hippolytidae) in the East Atlantic Ocean and the Mediterranean Sea, with a checklist of all
species in the genus. Zool Verhand 303:1–133
56. Zupo V, Messina P, Buttino I, Sagi A, Avila C, Nappo M, Bastida J, Codina C, Zupo S (2007)
Do benthic and planktonic diatoms produce equivalent effects in crustaceans? Mar Freshw
Behav Physiol 40:1–13. https://doi.org/10.1080/10236240701592930
57. Buia MC, Gambi MC, Zupo V (2000) Structure and functioning of Mediterranean seagrass
ecosystems: an overview. Biol Mar Medit 7(2):167–190
58. Charniaux-Cotton H (1967) Endocrinologie et génétique de la différenciation sexuelle chez
les invertébrés. C R Seances Soc Biol 16:6–9
59. Levy T, Manor R, Tamone SL, Aflalo ED, Sagi A (2017) Sexual differentiation during the life
history of a protandric shrimp. Integr Comp Biol 57(1):E327–E327
60. Bortolini JL, Bauet RT (2017) Persistence of reduced androgenic glands after protandric sex
change is a possible basis for simultaneous hermaphroditism in the marine shrimp Lysmata
wurdemanni. Integr Comp Biol 57(1):E208
61. Zupo V, Messina P, Carcaterra A, Aflalo ED, Sagi A (2008) Experimental evidence of a sex
reversal process in the shrimp Hippolyte inermis. Invertebr Reprod Dev 52(1–2):93–100
62. Reverberi G (1950) La situazione sessuale di Hippolyte viridis e le condizioni che la reggono.
Boll Zoologico 4:91–94
63. Zupo V (2001) Influence of diet on sex differentiation of Hippolyte inermis Leach (Decapoda:
Natantia) in the field. Hydrobiologia 449:131–140
64. Cobos V, Diaz V, Raso G, Enrique J, Manjon-Cabeza ME (2005) Insights on the female
reproductive system in Hippolyte inermis (Decapoda, Caridea): is this species really hermaphroditic? Invertebr Biol 124:310–320
65. Charnov EL, Los-den Hartogh RL, Jones WT, van den Assem J (1981) Sex ratio evolution in
a variable environment. Nature 289:27–33
66. Charnov EL (1982) The theory of sex allocation. Princeton University Press, Princeton, NJ,
USA
67. Zupo V, Jüttner F, Maibam C, Butera E, Blom JF (2014) Apoptogenic metabolites in fractions
of the benthic diatom Cocconeis scutellum parva. Mar Drugs 12:547–567. https://doi.org/
10.3390/md12010547
68. Juettner F, Messina P, Patalano C et al (2010) Odour compounds of the diatom Cocconeis
scutellum: effects on benthic herbivores living on Posidonia oceanica. Mar Ecol Prog Ser
400:63–73
7 Co-evolution of the Shrimp Hippolyte inermis and the Diatoms Cocconeis. . .
147