31. Leflaive J, Ten-Hage L (2009) Chemical interactions in diatoms: role of polyunsaturated
aldehydes and precursors. New Phytol 184:794–805. https://doi.org/10.1111/j.1469-8137.20
09.03033.x
32. Romano G, Russo GL, Buttino I, Ianora A, Miralto A (2003) A marine diatom-derived aldehyde
induces apoptosis in copepod and sea urchin embryos. J Exp Biol 206:3487–3494. https://doi.
org/10.1242/jeb.00580
33. Romano G, Miralto A, Ianora A (2010) Teratogenic effects of diatom metabolites on sea urchin
Paracentrotus lividus embryos. Mar Drugs 8:950–967. https://doi.org/10.3390/md8040950
34. Fink P (2007) Ecological functions of volatile organic compounds in aquatic systems.
Mar Freshw Behav Physiol 40:155–168. https://doi.org/10.1080/10236240701602218
35. Jones RH, Flynn KJ (2015) Nutritional status and diet composition affect the value of diatoms
as copepod prey. Science 307:1457–1459. https://doi.org/10.1126/science.1107767
36. Djeghri N, Atkinson A, Fileman ES et al (2018) High prey-predator size ratios and unselective
feeding in copepods: a seasonal comparison of five species with contrasting feeding modes.
Prog Oceanogr 16:63–74
37. Lepoint G, Cox AS, Dauby P, Poulicek M, Gobert S (2006) Food sources of two detritivore
amphipods associated with the seagrass Posidonia oceanica leaf litter. Mar Biol Res 2:355–365.
https://doi.org/10.1080/17451000600962797
38. Mazzella L, Russo GF (1989) Grazing effect of two Gibbula species (Mollusca,
Archaeogastropoda) on the epiphytic community of Posidonia oceanica leaves. Aquat Bot
35:353–373. https://doi.org/10.1016/0304-3770(89)90007-7
39. Jüttner F (1999) Allelochemical control of natural photoautotrophic biofilms. In: Keevil CW,
Godfree A, Holt D, Dow C (eds) Biofilms in aquatic environment. Royal Society of Chemistry,
Cambridge, UK, pp 43–50
40. De Stefano M, Marino D, Mazzella L (2000) Marine taxa of Cocconeis on leaves of Posidonia
oceanica, including a new species and two new varieties. Eur J Phycol 35:225–242. https://doi.
org/10.1080/09670260010001735831
41. Watson SB, Ridal J (2004) Periphyton: a primary source of widespread and severe taste and
odour. Water Sci Technol 49:33–39
42. Raniello R, Iannicelli MM, Nappo M Avila C, Zupo V (2006) Production of Cocconeis
neothumensis (Bacillariophyceae) biomass in batch cultures and bioreactors for biotechnological applications: light and nutrient requirements. J Appl Phycol. https://doi.org/10.1007/
s10811-006-9145-4
43. Zupo V, Alexander T, Edgar GJ (2017) Relating trophic resources to community structure: a
predictive index of food availability. R Soc Open Sci 4:160515. https://doi.org/10.1098/
rsos.160515
44. Zupo V, Messina P (2006) How do dietary diatoms cause the sex reversal of the shrimp
Hippolyte inermis Leach (Crustacea, Decapoda). Mar Biol 151:907–917. https://doi.org/
10.1007/s00227-006-0524-9
45. Zariquiei Alvarez R (1968) Crustaceos Decapodos ibericos. Invest Pesq 32:1–510
46. Gambi MC, Lorenti M, Russo GF, Scipione MB, Zupo V (1992) Depth and seasonal distribution of some groups of the vagile fauna of the Posidonia oceanica leaf stratum: structural and
trophic analyses. PSZNI Mar Ecol 13(1):17–39
47. Guillen Nieto JE (1990) Guia illustrada de los crustaceos decapo- dos del litoral alicantino.
Instituto del Cultura “Juan Gil-Albert” Publisher, Alicante. 316 pp
48. Bedini R, Canali MG, Acunto S (1997) Study of the mobile fauna of Posidonia oceanica (L.)
Delile of Golfo di Follonica e Golfo di baratti. In: Ambiente Mare: Ecologia e nuove Tecnologie
di Ricerca. Edizioni Regione Toscana, Collana Ricerca Scientifica e Tecnologica 12:59–78
49. Ianora A, Poulet SA, Miralto A (1995) A comparative study of the inhibitory effect of diatoms
on the reproductive biology of the copepod Temora stylifera. Mar Biol 121:533–539
50. Poulet SA, Ianora A, Miralto A, Meijer L (1994) Do diatoms arrest embryonic development in
copepods? Mar Ecol Progr Ser 111:79–86
146
V. Zupo
aldehydes and precursors. New Phytol 184:794–805. https://doi.org/10.1111/j.1469-8137.20
09.03033.x
32. Romano G, Russo GL, Buttino I, Ianora A, Miralto A (2003) A marine diatom-derived aldehyde
induces apoptosis in copepod and sea urchin embryos. J Exp Biol 206:3487–3494. https://doi.
org/10.1242/jeb.00580
33. Romano G, Miralto A, Ianora A (2010) Teratogenic effects of diatom metabolites on sea urchin
Paracentrotus lividus embryos. Mar Drugs 8:950–967. https://doi.org/10.3390/md8040950
34. Fink P (2007) Ecological functions of volatile organic compounds in aquatic systems.
Mar Freshw Behav Physiol 40:155–168. https://doi.org/10.1080/10236240701602218
35. Jones RH, Flynn KJ (2015) Nutritional status and diet composition affect the value of diatoms
as copepod prey. Science 307:1457–1459. https://doi.org/10.1126/science.1107767
36. Djeghri N, Atkinson A, Fileman ES et al (2018) High prey-predator size ratios and unselective
feeding in copepods: a seasonal comparison of five species with contrasting feeding modes.
Prog Oceanogr 16:63–74
37. Lepoint G, Cox AS, Dauby P, Poulicek M, Gobert S (2006) Food sources of two detritivore
amphipods associated with the seagrass Posidonia oceanica leaf litter. Mar Biol Res 2:355–365.
https://doi.org/10.1080/17451000600962797
38. Mazzella L, Russo GF (1989) Grazing effect of two Gibbula species (Mollusca,
Archaeogastropoda) on the epiphytic community of Posidonia oceanica leaves. Aquat Bot
35:353–373. https://doi.org/10.1016/0304-3770(89)90007-7
39. Jüttner F (1999) Allelochemical control of natural photoautotrophic biofilms. In: Keevil CW,
Godfree A, Holt D, Dow C (eds) Biofilms in aquatic environment. Royal Society of Chemistry,
Cambridge, UK, pp 43–50
40. De Stefano M, Marino D, Mazzella L (2000) Marine taxa of Cocconeis on leaves of Posidonia
oceanica, including a new species and two new varieties. Eur J Phycol 35:225–242. https://doi.
org/10.1080/09670260010001735831
41. Watson SB, Ridal J (2004) Periphyton: a primary source of widespread and severe taste and
odour. Water Sci Technol 49:33–39
42. Raniello R, Iannicelli MM, Nappo M Avila C, Zupo V (2006) Production of Cocconeis
neothumensis (Bacillariophyceae) biomass in batch cultures and bioreactors for biotechnological applications: light and nutrient requirements. J Appl Phycol. https://doi.org/10.1007/
s10811-006-9145-4
43. Zupo V, Alexander T, Edgar GJ (2017) Relating trophic resources to community structure: a
predictive index of food availability. R Soc Open Sci 4:160515. https://doi.org/10.1098/
rsos.160515
44. Zupo V, Messina P (2006) How do dietary diatoms cause the sex reversal of the shrimp
Hippolyte inermis Leach (Crustacea, Decapoda). Mar Biol 151:907–917. https://doi.org/
10.1007/s00227-006-0524-9
45. Zariquiei Alvarez R (1968) Crustaceos Decapodos ibericos. Invest Pesq 32:1–510
46. Gambi MC, Lorenti M, Russo GF, Scipione MB, Zupo V (1992) Depth and seasonal distribution of some groups of the vagile fauna of the Posidonia oceanica leaf stratum: structural and
trophic analyses. PSZNI Mar Ecol 13(1):17–39
47. Guillen Nieto JE (1990) Guia illustrada de los crustaceos decapo- dos del litoral alicantino.
Instituto del Cultura “Juan Gil-Albert” Publisher, Alicante. 316 pp
48. Bedini R, Canali MG, Acunto S (1997) Study of the mobile fauna of Posidonia oceanica (L.)
Delile of Golfo di Follonica e Golfo di baratti. In: Ambiente Mare: Ecologia e nuove Tecnologie
di Ricerca. Edizioni Regione Toscana, Collana Ricerca Scientifica e Tecnologica 12:59–78
49. Ianora A, Poulet SA, Miralto A (1995) A comparative study of the inhibitory effect of diatoms
on the reproductive biology of the copepod Temora stylifera. Mar Biol 121:533–539
50. Poulet SA, Ianora A, Miralto A, Meijer L (1994) Do diatoms arrest embryonic development in
copepods? Mar Ecol Progr Ser 111:79–86
146
V. Zupo