Synthesis toward a global model of metabolism and chemical composition of medusae and ctenophores

Journal of Experimental Marine Biology and Ecology

Volumn 456, Issue , 2014, Pages 50-64

  Ikeda, Tsutomu ^a  

^a NONE   (Japan)

Author keywords

Ammonia excretion; CN composition; Ctenophores; Medusae; O:N ratio; Respiration

Indexed keywords

EID: 84898431843     PISSN: 00220981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jembe.2014.03.006     Document Type: Article

References (97)

1. Acuña J.L., López-Urrutia A., Colin S. Faking giants: the evolution of high prey clearance rates in jellyfishes. Science 2011, 333:1627-1629.
2. Arai M.N. A Functional Biology of Scyphozoa 1997, Chapman & Hall, London.
3. Arai M.N., Ford J.A., Whyte J.N.C. Biochemical composition of fed and starved Aequorea victoria (Murbach et Shearer, 1902)(Hydromedusa). J. Exp. Mar. Biol. Ecol. 1989, 127:289-299.
4. Bailey T.G., Torres J.J., Youngbluth M.J., Owen G.P. Effect of decompression on mesopelagic gelatinous zooplankton: a comparison of in situ and shipboard measurements of metabolism. Mar. Ecol. Prog. Ser. 1994, 113:13-27.
5. Bailey T.G., Youngbluth M.J., Owen G.P. Chemical composition and oxygen consumption rates of the ctenophore Bolinopsis infundibulum from the Gulf of Maine. J. Plankton Res. 1994, 16:673-689.
6. Bailey T.G., Youngbluth M.J., Owen G.P. Chemical composition and metabolic rates of gelatinous zooplankton from midwater and benthic boundary layer environments off Cape Hatteras, North Carolina, USA. Mar. Ecol. Prog. Ser. 1995, 122:121-134.
7. Båmstedt U. Seasonal excretion rates of macrozooplankton from the Swedish west coast. Limnol. Oceanogr. 1985, 30:607-617.
8. Biggs D.C. Respiration and ammonia excretion by open ocean gelatinous zooplankton. Limnol. Oceanogr. 1977, 22:108-117.
9. Brey T. An empirical model for estimating aquatic invertebrate respiration. Methods Ecol. Evol. 2010, 1:92-101.
10. Brotz L., Cheung W.W.L., Kleisner K., Pakhomov E., Pauly D. Increasing jellyfish populations: trends in large marine ecosystems. Hydrobiologia 2012, 690:3-20.
11. Childress J.J. Are there physiological and biochemical adaptation of metabolism in deep-sea animals?. Trends Ecol. Evol. 1995, 10:30-36.
12. Childress J.J., Nygaard M. The chemical composition and relative buoyancy of midwater crustaceans as a function of depth off Southern California. Mar. Biol. 1974, 27:225-238.
13. Childress J.J., Thuesen E.V. Effects of hydrostatic pressure on metabolic rates of six species of deep-sea gelatinous zooplankton. Limnol. Oceanogr. 1993, 38:665-670.
14. Clarke A. The adaptation of aquatic animals to low temperatures. The Effects of Low Temperatures on Biological Systems 1987, 315-348. Edward Arnold, London. B.W.W. Grout, G.J. Morris (Eds.).
15. Clarke A., Fraser K.P.P. Why does metabolism scale with temperature?. Funct. Ecol. 2004, 18:243-251.
16. Clarke A., Johnston N.M. Scaling of metabolic rate with body mass and temperature in teleost fish. J. Anim. Ecol. 1999, 68:893-905.
17. Clarke A., Holmes L.J., Gore D.J. Proximate and elemental composition of gelatinous zooplankton from the Southern Ocean. J. Exp. Mar. Biol. Ecol. 1992, 155:55-68.
18. Costello J. Complete carbon and nitrogen budgets for the hydromedusa Cladonema californicum (Anthomedusa: Cladonemidae). Mar. Biol. 1991, 108:119-128.
19. Davenport J., Trueman E.R. Oxygen uptake and buoyancy in zooplanktonic organisms from the tropical eastern Atlantic. Comp. Biochem. Physiol. 1985, 81A:857-863.
20. Doyle T.K., Houghton J.D.R., McDevitt R., Davenport J., Hays G.C. The energy density of jellyfish: estimates from bomb-calorimetry and proximate-composition. J. Exp. Mar. Biol. Ecol. 2007, 343:239-252.
21. Finenko G.A., Anninsky B.E., Romanova Z.A., Abolmasova G.I., Kideys A.E. Chemical composition, respiration and feeding rates of the new alien ctenophore, Beroe ovata, in the Black Sea. Hydrobiologia 2001, 451:177-186.
22. Finenko G.A., Kideys A.E., Anninsky B.E., Shiganova T.A., Roohi A., Tabari M.R., Rostami H., Bagheri S. Invasive ctenophore Mnemiopsis leidyi in the Caspian Sea: feeding, respiration, reproduction and predatory impact on the zooplankton community. Mar. Ecol. Prog. Ser. 2006, 314:171-185.
23. Gillenberg G., Greve W. Studies on oxygen uptake in ctenophores. Ann. Zool. Fenn. 1979, 16:44-49.
24. Gillooly J.F., Brown J.H., West G.B., Savage V.M., Charnov E.L. Effects of size and temperature on metabolic rate. Science 2001, 293:2248-2251.
25. Glazer D.S. The 3/4-power law is not universal: evolution of isometric, ontogenetic metabolic scaling in pelagic animals. Bioscience 2006, 56:325-332.
26. Gnaiger E., Bitterlich G. Proximate biochemical composition and caloric content calculated from elemental CHN analysis: a stoichiometric concept. Oecologia (Berlin) 1984, 62:289-298.
27. Hirst A.G., Roff J.C., Lampitt R.S. A synthesis of growth rates in marine epipelagic invertebrate zooplankton. Adv. Mar. Sci. 2003, 44:1-142.
28. Hoeger U. Biochemical composition of ctenophores. J. Exp. Mar. Biol. Ecol. 1983, 72:251-261.
29. Iguchi N., Ikeda T. Metabolism and elemental composition of aggregate and solitary forms of Salpa thompsoni (Tunicata: Thaliacea) in waters off the Antarctic Peninsula during austral summer 1999. J. Plankton Res. 2004, 26:1025-1037.
30. Ikeda T. Nutritional ecology of marine zooplankton. Mem. Fac. Fish. Hokkaido Univ. 1974, 22:1-97.
31. Ikeda T. The effect of laboratory conditions on the extrapolation of experimental measurements to the ecology of marine zooplankton. IV. Changes in respiration and excretion rates of boreal zooplankton species maintained under fed and starved conditions. Mar. Biol. 1977, 41:241-252.
32. Ikeda T. Metabolic rates of epipelagic marine zooplankton as a function of body mass and temperature. Mar. Biol. 1985, 85:1-11.
33. Ikeda T. Metabolism in mesopelagic and bathypelagic copepods: reply to Childress et al. (2008). Mar. Ecol. Prog. Ser. 2008, 373:193-196.
34. Ikeda T. Metabolism and chemical composition of zooplankton from 500 to 5000m depth of the western subarctic Pacific Ocean. J. Oceanogr. 2012, 68:641-649.
35. Ikeda T. Respiration and ammonia excretion of euphausiid crustaceans: synthesis towards a global-bathymetric model. Mar. Biol. 2013, 160:251-262.
36. Ikeda T. Synthesis toward a global-bathymetric model of metabolism and chemical composition of mysid crustaceans. J. Exp. Mar. Biol. Ecol. 2013, 445:79-87.
37. Ikeda T. Metabolism and chemical composition of marine pelagic amphipods: synthesis towards a global-bathymetric model. J. Oceanogr. 2013, 69:339-355.
38. Ikeda T., Bruce B. Metabolic activity and elemental composition of krill and other zooplankton from Prydz Bay, Antarctica, during early summer (November-December). Mar. Biol. 1986, 92:545-555.
39. Ikeda T., Hirakawa K. Metabolism and body composition of zooplankton in the cold mesopelagic zone of the southern Japan Sea. Plankton Biol. Ecol. 1998, 45:31-44.
40. Ikeda T., Mitchell A.W. Oxygen uptake, ammonia excretion, and phosphate excretion of krill and other Antarctic zooplankton, in relation to their body size and chemical composition. Mar. Biol. 1982, 71:283-298.
41. Ikeda T., Skjoldal H.R. Metabolism and elemental composition of zooplankton from the Barents Sea during early arctic summer. Mar. Biol. 1989, 100:173-183.
42. Ikeda T., Takahashi T. Synthesis towards a global-bathymetric model of metabolism and chemical composition of marine pelagic chaetognaths. J. Exp. Mar. Biol. Ecol. 2012, 424-425:78-88.
43. Ikeda T., Torres J.J., Hernández-León S., Geiger S.P. Metabolism. ICES Zooplankton Methodology Manual 2000, 455-532. Academic Press, San Diego. R.P. Harris, P.H. Wiebe, J. Lenz, H.R. Skjoldal, M. Huntley (Eds.).
44. Ikeda T., Sano F., Yamaguchi A., Matsuishi T. Metabolism of mesopelagic and bathypelagic copepods in the western North Pacific Ocean. Mar. Ecol. Prog. Ser. 2006, 322:199-211.
45. Ikeda T., Yamaguchi A., Matsuishi T. Chemical composition and energy content of deep-sea calanoid copepods in the western North Pacific Ocean. Deep-Sea Res. I 2006, 53:1791-1809.
46. Ikeda T., Sano F., Yamaguchi A. Respiration in marine pelagic copepods: a global-bathymetric model. Mar. Ecol. Prog. Ser. 2007, 339:215-219.
47. Ivleva I.V. The dependence of crustacean respiration rate on body mass and habitat temperature. Int. Rev. Ges. Hydrobiol. 1980, 65:1-47.
48. Kasuya T., Ishimaru T., Murano M. Metabolic characteristics of the lobate ctenophore Bolinopsis midado (Moser). Plankton Biol. Ecol. 2000, 47:114-121.
49. Kinosita J., Hiromi J., Kadota S. Do respiratory metabolic rates of the scyphomedusa Aurelia aurita scale isometrically throughout ontogeny in a sexual generation?. Hydrobiologia 1997, 347:51-55.
50. KiØrboe T., MØhlenberg F., Hamburger K. Bioenergetics of the planktonic copepod Acartia tonsa: relation between feeding, egg production and respiration, and composition of specific dynamic action. Mar. Ecol. Prog. Ser. 1985, 26:85-97.
51. Kremer P. Respiration and excretion by the ctenophore Mneopiopsis leidyi. Mar. Biol. 1977, 44:43-50.
52. Kremer P. Effect of food availability on the metabolism of the ctenophore Mnemiopsis mccradyi. Mar. Biol. 1982, 71:149-156.
53. Kremer P., Canino M.F., Gilmer R.W. Metabolism of epipelagic tropical ctenophore. Mar. Biol. 1986, 90:403-412.
54. Kruse S., Brey T., Bathmann U. Role of midwater chaetognaths in Southern Ocean pelagic energy flow. Mar. Ecol. Prog. Ser. 2010, 416:105-113.
55. Larson R.J. Water content, organic content, and carbon and nitrogen composition of medusa from the Northeast Pacific. J. Exp. Mar. Biol. Ecol. 1986, 99:107-120.
56. Larson R.J. Respiration and carbon turnover rates of medusae from the NE Pacific. Comp. Biochem. Physiol. 1987, 87A:93-100.
57. Larson R.J. Costs of transport for the scyphomedusa Stomolophus meleagris L. Can. J. Zool. 1987, 65:2690-2695.
58. Larson R.J., Harbison G.R. Source and fate of lipids in polar gelatinous zooplankton. Arctic 1989, 42:339-346.
59. Lee R.F., Hagen W., Kattner G. Lipid storage in marine zooplankton. Mar. Ecol. Prog. Ser. 2006, 307:273-306.
60. Lucus C.H., Pitt K.A., Purcell J.E., Lebrato M., Condon R.H. What's in a jellyfish? Proximate and elemental composition and biometric relationships for use in biogeochemical studies. Ecology 2011, 92:1704. (Ecological Archives E092-144-D1).
61. Marshalones D., Pinckney J.L. Respiration rates of dominant hydromedusae in the North Inlet tidal estuary during winter and summer. J. Plankton Res. 2007, 29:1031-1040.
62. Mayzaud P., Conover R.J. O:N atomic ratio as a tool to describe zooplankton metabolism. Mar. Ecol. Prog. Ser. 1988, 45:289-302.
63. McCloskey L.R., Muscatine L., Wilkerson F.P. Daily photosynthesis, respiration, and carbon budgets in a tropical jellyfish (Mastigias sp.). Mar. Biol. 1994, 119:13-22.
64. Mills C.E. Medusae, siphonophores, and ctenophores as planktivorous predators in changing global ecosystems. ICES J. Mar. Sci. 1995, 52:575-581.
65. MØller L.F., Riisgård H.U. Respiration in the scyphozoan jellyfish Aurelia aurita and two hydromedusae (Sarsia tubulosa and Aequorea vitrina): effect of size, temperature and growth. Mar. Ecol. Prog. Ser. 2007, 330:149-154.
66. Morand P., Carre C., Biggs D.C. Feeding and metabolism of the jellyfish Pelagia noctiluca (scyphomedusae, semaeostomae). J. Plankton Res. 1987, 9:651-665.
67. Nakaya F., Saito Y., Motokawa T. Experimental allometry: effect of size manipulation on metabolic rate of colonial ascidians. Proc. R. Soc. B 2005, 272:1963-1969.
68. Nemazie D.A., Purcell J.E., Gilbert P.M. Ammonium excretion by gelatinous zooplankton and their contribution to the ammonium requirements of microplankton in Chesapeake By. Mar. Biol. 1993, 116:451-458.
69. Nival P., Nival S., Palazzoli I. Données sur la respiration de différent organismes communs dans le plankton de Villefranche-sur-Mer. Mar. Biol. 1972, 17:63-76.
70. Omori M., Ikeda T. Methods in Marine Zooplankton Ecology 1984, John Wiley and Sons Inc., USA.
71. Parsons T.R., Lalli C.M. Jellyfish population explosions: revisiting a hypothesis of possible causes. La Mer 2002, 40:111-121.
72. Percy J.A. Influence of season, size, and temperature on the metabolism of an arctic cyppid ctenophore, Mertensia ovum (Fabricius). Sarsia 1988, 73:61-70.
73. Pitt K.A., Koop K., Rissik D. Contrasting contributions to inorganic nutrient recycling by the co-occurring jellyfishes, Catostylus mosaicus and Phyllorihiza punctata (Scyphozoa, Rhizostomeae). J. Exp. Mar. Biol. Ecol. 2005, 315:71-86.
74. Pitt K.A., Welsh D.T., Condon R.H. Influence of jellyfish blooms on carbon, nitrogen and phosphorus cycling and plankton production. Hydrobiologia 2009, 616:133-149.
75. Pitt K.A., Duarte C.M., Lucas C.H., Sutherland K.R., Condon R.H., Mianzan H., Purcell J.E., Robinson K.L., Uye S. Jellyfish body plans provide allometric advantates beyond low carbon content. PLoS One 2013, 8:2-10.
76. Postel L., Fock H., Hagen W. Biomass and abundance. ICES Zooplankton Methodology Manual 2000, 83-192. Academic Press, San Diego. R.P. Harris, P.H. Wiebe, J. Lenz, H.R. Skjoldal, M. Huntley (Eds.).
77. Purcell J.E. A review of cnidarians and ctenophores feeding on competitors in the plankton. Hydrobiologia 1991, 216(217):335-342.
78. Purcell J.E. Extension of methods for jellyfish and ctenophore trophic ecology to large-scale research. Hydrobiologia 2009, 616:23-50.
79. Purcell J.E., Uye S., Lo W.-T. Anthropogenic causes of jellyfish blooms and their direct consequences for humans: a review. Mar. Ecol. Prog. Ser. 2007, 350:153-174.
80. Purcell J.E., Fuentes V., Atienza D., Tilves U., Astorga D., Kawahara M., Hays G. Use of respiration rates of scyphozoan jellyfish to estimate their effects on the food web. Hydrobiologia 2010, 645:135-152.
81. Raymont J.E.G. Plankton and productivity in the oceans. Zooplankton 1983, vol. 2. Pergamon Press, Oxford.
82. Reeve M.R., Syms M.A., Kremer P. Growth dynamics of a ctenophore (Mnemiopsis) in relation to variable food supply. I. Carbon biomass, feeding, egg production, growth and assimilation efficiency. J. Plankton Res. 1989, 11:535-552.
83. Schneider G. The common jellyfish Aurelia aurita: standing stock, excretion and nutrient regeneration in the Kiel Bight, Western Baltic. Mar. Biol. 1989, 100:507-514.
84. Schneider G. A comparison of carbon based ammonia excretion rates between gelatinous and non-gelatinous zooplankton: implications and consequences. Mar. Biol. 1990, 106:219-225.
85. Scolardi K.M., Daly K.L., Pakhomov E.A., Torres J.J. Feeding ecology and metabolism of the Antarctic cydippid ctenophore Callianira antarctica. Mar. Ecol. Prog. Ser. 2006, 317:111-126.
86. Seibel B.A., Drazen J.C. The rate of metabolism in marine animals: environmental constraints, ecological demands and energetic opportunities. Philos. Trans. R. Soc. B 2007, 362:2061-2078.
87. Shimauchi H., Uye S. Excretion and respiration rates of the scyphomedusa Aurelia aurita from the inland sea of Japan. J. Oceanogr. 2007, 63:27-34.
88. Smith K.L. Zooplankton of a bathyal benthic boundary layer: In situ rates of oxygen consumption and ammonium excretion. Limnol. Oceanogr. 1982, 27:461-471.
89. Sokal R.R., Rohlf F.J. Biometry. The principles and Practice of Statistics in Biological Research 1995, Freeman, New York.
90. Svetlichny L.S., Abolmasova G.I., Hubareva E.S., Finenko G.A., Bat L., Kideys A.E. Respiration rates of Beroe ovata in the Black Sea. Mar. Biol. 2004, 145:585-593.
91. Thor P. Relationship between specific dynamic action and protein deposition in calanoid copepods. J. Exp. Mar. Biol. Ecol. 2000, 245:171-182.
92. Thuesen E.V., Childress J.J. Oxygen consumption rates and metabolic enzyme activities of oceanic California medusae in relation to body size and habitat depth. Biol. Bull. 1994, 187:84-98.
93. Uye S., Shimauchi H. Population biomass, feeding, respiration and growth rates, and carbon budgets of the scyphomedusa Aurelia aurita in the Inland Sea of Japan. J. Plankton Res. 2005, 27:237-248.
94. Ventura M. Linking biochemical and elemental composition in freshwater and marine crustacean zooplankton. Mar. Ecol. Prog. Ser. 2006, 327:233-246.
95. Verde E.A., McCloskey L.R. Production, respiration, and photophysiology of the mangrove jellyfish Cassiopea xamachana symbiotic with zooxanthellae: effect of jellyfish size and season. Mar. Ecol. Prog. Ser. 1998, 168:147-162.
96. Youngbluth M.J., Båmstedt U. Distribution, abundance, behavior and metabolism of Periphylla periphylla, a mesopelagic coronate medusa in a Norwegian fjord. Hydrobiologia 2001, 451:321-333.
97. Youngbluth M.J., Kremer P., Bailey T.G., Jacoby C.A. Chemical composition, metabolic rates and feeding behavior of the midwater ctenophore Bathocyroe fosteri. Mar. Biol. 1988, 98:87-94.