UV-tolerance and instantaneous physiological stress responses of two Antarctic amphipod species Gondogeneia antarctica and Djerboa furcipes during exposure to UV radiation

Marine Environmental Research

Volumn 64, Issue 3, 2007, Pages 267-285

  Obermüller, Birgit ^a   Puntarulo, Susana ^b   Abele, Doris ^c  

^a BRITISH ANTARCTIC SURVEY   (United Kingdom)

^b UNIVERSIDAD DE BUENOS AIRES   (Argentina)

^c ALFRED WEGENER INSTITUTE FOR POLAR AND MARINE RESEARCH   (Germany)

Author keywords

Amphipods; Oxygen consumption; Photoprotection; Stress response; UV radiation

Indexed keywords

ANIMALS; METABOLISM; OXYGEN; RADIATION SHIELDING; SOLAR ENERGY;

AMPHIPODS; OXYGEN CONSUMPTION; PHOTOPROTECTION; STRESS RESPONSE;

ULTRAVIOLET RADIATION;

AMINO ACID; CAROTENOID; CATALASE; SUNSCREEN;

AMPHIPOD; DOSE-RESPONSE RELATIONSHIP; ENZYME ACTIVITY; INHIBITION; METABOLISM; OXYGEN CONSUMPTION; PHYSIOLOGICAL RESPONSE; RADIATION EXPOSURE; STRESS; SUBLETHAL EFFECT; TOLERANCE; ULTRAVIOLET RADIATION;

AMPHIPODA; ANIMAL BEHAVIOR; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL REGENERATION; DJERBOA FURCIPES; ENZYME INHIBITION; GONDOGENEIA ANTARCTICA; LIGHT ABSORPTION; METABOLIC RATE; NONHUMAN; OXYGEN CONSUMPTION; PHOTOSYNTHESIS; PHYSIOLOGICAL STRESS; RADIATION ABSORPTION; RADIATION DOSE; RADIATION EXPOSURE; RADIATION INJURY; RADIATION SHIELD; ULTRAVIOLET A RADIATION; ULTRAVIOLET B RADIATION; ULTRAVIOLET RADIATION;

ADAPTATION, PHYSIOLOGICAL; AMPHIPODA; ANIMALS; ANTARCTIC REGIONS; OXYGEN CONSUMPTION; STRESS; ULTRAVIOLET RAYS;

ANTARCTICA;

AMPHIPODA; ANIMALIA; GONDOGENEIA ANTARCTICA;

EID: 34547462165     PISSN: 01411136     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.marenvres.2007.02.001     Document Type: Article

References (49)

1. Abele D., and Puntarulo S. Formation of reactive species and induction of antioxidant defence systems in polar and temperate marine invertebrates and fish. Rev. Comput. Biochem. Physiol. 138A (2004) 405-415
2. Abele D., Burlando B., Viarengo A., and Pörtner H.-O. Exposure to elevated temperatures and hydrogen peroxide elicits oxidative stress and antioxidant response in the Antarctic intertidal limpet Nacella concinna. Comp. Biochem. Physiol. 120B (1998) 425-435
3. 2 accumulation from photochemical production and atmospheric wet deposition in Antarctic coastal and off-shore waters of Potter Cove, King George Island, South Shetland Islands. Antarct. Sci. 11 (1999) 131-139
4. Abele-Oeschger D., Sartoris F.J., and Pörtner H.-O. Hydrogen peroxide causes a decrease in aerobic metabolic rate and in intracellular pH in the shrimp Crangon crangon. Comp. Biochem. Physiol. 117C (1997) 123-129
5. Boveris A. Biochemistry of free radicals: from electrons to tissues. Medicina 58 (1998) 350-356
6. Carefoot T.H., Karentz D., Pennings S.C., and Young C.L. Distribution of mycosporine-like amino acids in the sea hare Aplysia dactylomela: effects of diet on amounts and types sequestered over time in tissues and spawn. Comp. Biochem. Physiol. 126C (2000) 91-104
7. Chapelle G., and Peck L.S. The influence of acclimation and substratum in the metabolism of the Antarctic amphipods Waldeckia obesa (Chevreux 1905) and Bovallia gigantea (Pfeffer 1888). Polar Biol. 15 (1995) 225-232
8. Chapelle G., Peck L.S., and Clarke A. Effects of feeding and starvation on the metabolic rate of the necrophagous Antarctic amphipod Waldeckia obesa (Chevreux, 1905). J. Exp. Mar. Biol. Ecol. 183 (1994) 63-76
9. Conde F.R., Churio M.S., and Previtali C.M. The photoprotector mechanism of mycosporine-like amino acids. Excited state properties and photostability of prophyra-334 in aqueous solution. J. Photochem. Photobiol. B. 56 (2000) 139-144
10. Denys C.J. Ommochrome pigments in the eyes of Euphausia superba (Crustacea, Euphausiacea). Polar Biol. 1 (1982) 69-76
11. Dethlefsen V., von Westernhagen H., Tüg H., Hansen P.D., and Dizer H. Influence of solar ultraviolet-B on pelagic fish embryos: osmolality, mortality and viable hatch. Helgol. Mar. Res. 55 (2001) 45-55
12. Dunlap W.C., and Shick J.M. Ultraviolet radiation-absorbing mycosporine-like amino acids in coral reef organisms: a biochemical and environmental perspective. J. Phycol. 34 (1998) 418-430
13. Dunlap W.C., Shick J.M., and Yamamoto Y. UV Protection in marine organisms. I. Sunscreens, oxidative stress and antioxidants. In: Yoshikawa T., Toyokuni S., Yamamoto Y., and Naito Y. (Eds). Free Radicals in Chemistry, Biology and Medicine (2000), OICA International, London 200-214
14. Gantchev T.G., and van Lier J.E. Catalase inactivation following photosensitization with tetrasulfonated metallophtalocyanines. Photochem. Photobiol. 62 (1995) 123-134
15. Goncalves R.J., Villafane V.E., and Helbling E.W. Photorepair activity and protective compounds in two freshwater zooplankton (Daphnia menucoensis and Metacyclops mendocinus) from Patagonia, Argentina. Photochem. Photobiol. Sci. 1 (2002) 996-1000
16. In: Halliwell B., and Gutteridge J.M. (Eds). Free Radicals in Biology and Medicine (1999), Oxford University Press, New York 936pp
17. Helbling E.W., Zaratti F., Sala L.O., Palenque E.R., Menchi C.F., and Villafañe V.E. Mycosporine-like amino acids protect the copepod Boeckella titicacae (Harding) against high levels of solar UVR. J. Plankton Res. 24 (2002) 225-234
18. Holm-Hansen O., Lubin D., and Helbling E.W. Ultraviolet radiation and its effects on organisms in aquatic environments. In: Young A.R., Björn L.O., Moan J., and Nultsch W. (Eds). Environmental UV Photobiology (1993), Plenum Press, New York 379-425
19. Jeffrey S.W. Phytoplankton Pigments in Oceanography: Guidelines to Modern Methods (1997), UNESCO Publications, Paris 661pp
20. Karentz D., McEuen F.S., Land M.C., and Dunlap W.C. Survey of mycosporine-like amino acid compounds in Antarctic marine organisms: potential protection from ultraviolet exposure. Mar. Biol. 108 (1991) 157-166
21. Leech D.M., and Johnsen S. Behavioral responses - UVR avoidance and vision. In: Helbling E.W., and Zagarese H. (Eds). UV Effects in Aquatic Organisms and Ecosystems. Comprehensive Series in Photochemistry and Photobiology vol. 1 (2003), The Royal Society of Chemistry, Springer Verlag, Cambridge, UK 455-481
22. Lesser M.P. Oxidative stress in marine environments: biochemistry and physiological ecology. Annu. Rev. Physiol. 68 (2006) 253-278
23. Levine R.L. Carbonyl modified proteins in cellular regulation, aging, and disease. Free Radical Biol. Med. 32 (2002) 790-796
24. Levine R.L., Garland D., Oliver C.N., Amici A., Climent I., Lenz A.-G., Ahn B.-W., Shaltiel S., and Stadtman E.R. Determination of carbonyl content in oxidatively modified proteins. Method Enzymol. 186 (1990) 464-485
25. Madronich S., McKenzie R.L., Björn L.O., and Caldwell M.M. Changes in biologically active ultraviolet radiation reaching the Earth's surface. J. Photochem. Photobiol. 46B (1998) 5-19
26. Malloy K.D., Holman M.A., Mitchell D., and Detrich III H.W. Solar UVB-induced DNA damage and photoenzymatic DNA repair in Antarctic zooplankton. Proc. Natl. Acad. Sci. 94 (1997) 1258-1263
27. Newman S.J., Nicol S., Ritz D., and Marchant H. Susceptibility of Antarctic krill (Euphausia superba Dana) to ultraviolet radiation. Polar Biol. 22 (1999) 50-55
28. Newman S.J., Dunlap W.C., Nicol S., and Ritz D. Antarctic krill (Euphausia superba) acquire a UV-absorbing mycosporine-like amino acid from dietary algae. J. Exp. Mar. Biol. Ecol. 255 (2000) 93-110
29. Newman S.J., Ritz D., and Nicol S. Behavioural reactions of Antarctic krill (Euphausia superba Dana) to ultraviolet and photosynthetically active radiation. J. Exp. Mar. Biol. Ecol. 297 (2003) 203-217
30. Obermüller, B., Abele, D. 2004. Different UVB-tolerance in herbivorous versus carnivorous amphipods from Kongsfjorden. In: Wiencke, C. (Ed.), The coastal ecosystem of Kongsfjorden, Svalbard. Synopsis of biological research performed at the Koldewey Station in the years 1991-2003. Rep. Polar Mar. Res., vol. 492, pp. 222-230.
31. Obermüller B., Karsten U., Pörtner H.-O., and Abele D. Effects of UV-radiation on oxidative stress parameters in polar marine amphipods, and the role of UV-absorbing mycosporine-like amino acids (MAAs) in their diet. In: Huiskes A.H.L., Gieskes W.W.C., Rozema R.M.L., Schorno S.M., Vies S.M., and Wolff W.J. (Eds). Antarctic Biology in a Global Context (2003), Backhuys Publishers, Leiden, The Netherlands 63-68
32. Obermüller B., Karsten U., and Abele D. Response of oxidative stress parameters and sunscreening compounds in Arctic amphipods during experimental exposure to maximal natural UVB radiation. J. Exp. Mar. Biol. Ecol. 323 (2005) 100-117
33. Opalinski K.W., and Sicinski J. Oxygen consumption in antarctic tidal zone amphipods. Pol. Arch. Hydrobiol. 42 (1995) 537-546
34. Philipp E., Brey T., Heilmayer O., Abele D., and Pörtner H.-O. Physiological ageing in a temperate and a polar swimming scallop. Mar. Ecol. Prog. Ser. 307 (2006) 187-198
35. Quetin L.B., Smith R.C., Patterson K., Ross R.M., Wyatt-Evans C., and Coe H. Palmer LTER: effects of ultraviolet radiation the behavior of larvae (Euphausia superba). N.Z. Nat. Sci. 23 Suppl (1998) 154
36. Rozema J., Björn L.O., Bornman J.F., Gaberscik A., Häder D.-P., Trost T., Germ M., Klisch M., Gröniger A., Sinha R.P., Lebert M., He Y.-Y., Buffoni-Hall R., de Bakker N.V.J., van de Staaij J., and Meijkamp B.B. The role of UV-B radiation in aquatic and terrestrial ecosystems - an experimental and functional analysis of the evolution of UV-absorbing compounds. J. Photochem. Photobiol. 66B (2002) 2-12
37. Sagi A., Rise M., Isam K., and Arad S.M. Carotenoids and their derivatives in organs of the maturing female crayfish Cherax quadricarinatus. Comp. Biochem. Physiol. 112B (1995) 309-313
38. Schiedt K., Bischof S., and Glinz E. Metabolism of carotenoids and in vivo racemization of (3S,3′S)-astaxanthin in the crustacean Penaeus. Method Enzymol. 214 (1993) 148-167
39. Shashar, N. 1994. UV vision by marine animals: mainly questions. In: Gulko, D., Jokiel, P.L. (eds.). Ultraviolet Radiation and Coral Reefs (HIMB Tech. Report #41). UNIHI-Sea Grant-CR-95-03, pp. 201-206.
40. Shick J.M., and Dunlap W.C. Mycosporine-like amino acids and related gadusols: Biosynthesis, accumulation, and UV-protective functions in aquatic organisms. Annu. Rev. Physiol. 64 (2002) 223-262
41. Storch D., Abele D., and Pörtner H.-O. The effect of hydrogen peroxide on isolated body wall of the lugworm Arenicola marina (L.) at different extracellular pH levels. Comp. Biochem. Physiol. 128C (2001) 391-399
42. Storz U.C., and Paul R.J. Phototaxis in water fleas (Daphnia magna) is differently influenced by visible and UV light. J. Comp. Physiol. A 183 (1998) 709-717
43. Vetter R.D., Kurtzman A., and Mori T. Diel cycles of DNA damage and repair in eggs and larvae of northern anchovy, Engraulis mordax, exposed to solar ultraviolet radiation. Photochem. Photobiol. 69 (1999) 27-33
44. Vincent W.F., and Roy S. Solar ultraviolet-B radiation and aquatic primary production: damage, protection, recovery. Environ. Rev. 1 (1993) 1-12
45. Williamson C.E., Zagarese H.E., Schulze P.C., Hargreaves B.R., and Seva J. The impact of short-term exposure to UV-B radiation on zooplankton communities in north temperate lakes. J. Plankton Res. 16 (1994) 205-218
46. Williamson C.E., Neale P.J., Grad G., De Lange H.J., and Hargreaves B.R. Beneficial and detrimental effects of UV on Aquatic organisms: implications of spectral variation. Ecol. Appl. 11 6 (2001) 1843-1857
47. WMO, 2002. Scientific assessment of ozone depletion 2002. World Meteorological Organization Global Ozone Research and Monitoring Project-Report No. 47.
48. Zellmer I.D., Arts M.T., Abele D., and Humbeck K. Evidence of sublethal damage in Daphnia (Cladocera) during exposure to solar UV radiation in subarctic ponds. Arctic Antarctic Alpine Res. 36 (2004) 370-377
49. Zigman S., Schultz J.B., and Schultz M. Measurement of oxygen production by in vitro human and animal lenses with an oxygen electrode. Curr. Eye Res. 17 2 (1998) 115-119