Phragmites australis and Quercus robur leaf extracts affect antioxidative system and photosynthesis of Ceratophyllum demersum

Ecotoxicology and Environmental Safety

Volumn 67, Issue 2, 2007, Pages 240-246

  Kamara, Sheku ^a   Pflugmacher, Stephan ^a  

^a LEIBNIZ INSTITUTE OF FRESHWATER ECOLOGY AND INLAND FISHERIES   (Germany)

Author keywords

Antioxidative enzymes; Ceratophyllum demersum; Dissolved organic carbon; Glutathione reductase; Glutathione S transferase; Lipid peroxidation; Peroxidase; Phragmites australis; Physiological stress; Quercus robur

Indexed keywords

DISSOLVED ORGANIC MATTER; GLUTATHIONE REDUCTASE; GLUTATHIONE TRANSFERASE; ORGANIC CARBON; OXYGEN; PEROXIDASE;

ANTIOXIDANT; DECIDUOUS TREE; DISSOLVED ORGANIC CARBON; ECOTOXICOLOGY; ENZYME ACTIVITY; GRASS; LEAF LITTER; LIPID; MACROPHYTE; PEROXY RADICAL; PHOTOSYNTHESIS; PHYSIOLOGICAL RESPONSE; PLANT EXTRACT; REEDBED; SENESCENCE; SUBMERGED VEGETATION; TOXIC SUBSTANCE; WATER POLLUTION;

ARTICLE; CERATOPHYLLUM DEMERSUM; CONTROLLED STUDY; ENZYME ACTIVITY; HORNWORT; LEAF LITTER; LIPID PEROXIDATION; MACROPHYTE; NONHUMAN; OAK; PHOTOSYNTHESIS; PHRAGMITES AUSTRALIS; QUERCUS ROBUR; STREAM (RIVER);

ANGIOSPERMS; ANTIOXIDANTS; LIPID PEROXIDATION; OXYGEN; PHOTOSYNTHESIS; PLANT EXTRACTS; PLANT LEAVES; POACEAE; QUERCUS; WATER POLLUTANTS, CHEMICAL;

CERATOPHYLLUM DEMERSUM; PHRAGMITES AUSTRALIS; QUERCUS ROBUR;

EID: 34247640651     PISSN: 01476513     EISSN: 10902414     Source Type: Journal    
DOI: 10.1016/j.ecoenv.2006.07.004     Document Type: Article

References (45)

1. Alin P., Danielson U.H., and Mannervik B. 4-hydroxyalk-2-enals are substrates for glutathione transferase. FEBS Lett. 179 2 (1984) 267-270
2. Bosch, E.V. D., Ward, B.G., Clarkson, B.D., 2004. Woolly Nightsahde (Solanum mauritianum) and its allelopathic effects on New Zealand native Hebe stricta seed germination. In: Proceedings of the 57th New Zealand Plant Protection Society Incorporation Conference, pp. 98-101.
3. Botsoglou N.A., Fletouris D.J., Papageorgiou G.E., Vassilopoulos V.N., Mantis A.J., and Trakatellis A.G. Rapid, sensitive, and specific thiobarbituric acid method for measuring lipid peroxidation in animal tissue, food, and feedstuff samples. J. Agric. Food Chem. 42 (1994) 1931-1937
4. Bradford M.M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein dye-binding. Anal. Biochem. 72 (1976) 248-254
5. Brooks P.D., McKnight D.M., and Bencala K.E. The relationship between soil heterotrophic activity, soil dissolved organic carbon (DOC) leachate, and catchment-scale DOC export in headwater catchments. Water Resour. Res. 35 (1999) 1895-1902
6. Byle T.D., Sutton H.D., and Klaine S.J. Evaluation of peroxidase as a biochemical indicator of toxic chemical exposure in the aquatic plant Hydrilla verticillata. Royle. Environ. Toxicol. Chem. (1994) 509-515
7. Carlberg I., and Mannervik B. Glutathione reductase. Methods Enzymol. 113 (1985) 484-490
8. Cole J.J., Pace M.L., Carpenter S.R., and Kitchell J.F. Persistence of net heterotrophy in lakes during nutrient addition and food web manipulations. Limnol. Oceanogr. 45 8 (2000) 1718-1730
9. DIN EN 1484, 1998. Anleitung zur Bestimmung des gesamten organischen Kohlenstoffs (TOC) und des gelösten organischen Kohlenstoffs. DEV, H3, 40, Lieferung.
10. Drotar A., Phelps P., and Fall R. Evidence for glutathione peroxidase activities in cultured plant cells. Plant Sci. 42 (1985) 35-40
11. Feeny P.P. Seasonal changes in oak leaf tannins and nutrients as a cause of spring feeding by winter moth caterpillars. Ecology 51 (1970) 565-581
12. Foyer C.H., Lescure J.C., Lefebvre C., Morot-Guadry J.F., Vincent M., and Vaucheret H. Adaptations of photosynthetic electron transport, carbon assimilation and carbon partitioning in transgenic Nicotiana plumbaginifolia plants to changes in nitrate reductase activity. Plant Physiol. 104 (1994) 171-178
13. Grene R. Oxidative stree and acclimation mechanisms in plants. The Arabidopsis Book. Am. Soc. Plant Biol. (2002) 1-20
14. Grundhöfer P., Niemetz R., Schilling G., and Gross G.G. Biosynthesis and subcellular distribution of hydrolyzable tannins. Phytochemistry 57 (2001) 915-927
15. Habig W., Pabst M.J., and Jakoby W.B. Glutathione S-transferase: the first step in mercapturic acid formation. J. Biol. Chem. 249 (1974) 1730-1739
16. Hollis, G.E., Jones, T.A., 1991. Europe and the Mediterranean Basin. In: Finlayson, M., Moser, M. (Eds.), Wetlands, pp. 27-56.
17. Hunter M.E., and Menges E.S. Allelopathic effects and root distribution of Ceratiola ericoides (Empetraceae) on seven Rosemary scrub species. Am. J. Bot. 89 7 (2002) 1113-1118
18. Jeppeson E., Sondergaard M., Kronvang B., Jensen J.P., Svendsen L.M., and Lauridsen T.L. Lake and catchment management in Denmark. Hydrobiologia 395/396 (1999) 419-432
19. Kruse, M., Strandberg, M., Strandberg, B., 2000. Ecological Effects of Allelopathic Plants-a Review. National Environmental Research Institute, Silkeborg, Denmark, 66pp., NERI Technical Report No. 315.
20. Kwak S.S., Kim S.K., Park I.H., and Liu J.R. Enhancement of peroxidase activity by stress-related chemicals in sweet potato. Phytochemistry 43 (1996) 565-568
21. May M.J., and Leaver C.J. Oxidative stimulation of glutathione synthesis in Arabidopsis thaliana suspension cultures. Plant Physiol. 103 (1993) 621-627
22. Menone M.L., and Pflugmacher S. Effects of 3-chlorobiphenyl on photosynthetic oxygen production, glutathione content and detoxication enzymes in the aquatic macrophyte Ceratophyllum demersum. Chemosphere 60 (2005) 79-84
23. Meyer J.L., Wallace J.B., and Eggert S.L. Leaf litter as a source of dissolved organic carbon in streams. Ecosystems 1 (1998) 240-249
24. Nimptsch J., Wunderlin D.A., Dollan A., and Pflugmacher S. Antioxidant and biotransformation enzymes in Myriophyllum quitense as biomarkers of heavy metal exposure and eutrophication in Suquia River basin (Cordoba, Argentina). Chemos 61 (2005) 147-157
25. Oberg L.G., Glas B., Swanson S.E., Rappe C., and Paul K.G. Peroxidas-catalyzed oxidation of chlorophenols to polychlorinated dibenzo-p-dioxins and dibenzofurans. Arch. Environ. Contam. Toxicol. 19 (1990) 930-938
26. Oettmeier W., Masson K., and Donner A. Anthraquinone inhibitors of photosystem II electron transport. FEBS Lett. 231 (1988) 259-262
27. Pflugmacher S., and Steinberg C.E.W. Activity of phase I and phase II detoxication enzymes in aquatic macrophytes. J. Appl. Bot. 71 (1997) 144-146
28. Pflugmacher S., Spangenberg M., and Steinberg C.E.W. Dissolved organic matter (DOM) and effects on the aquatic macrophyte Ceratophyllum demersum in relation to photosynthesis, pigment pattern and activity of detoxication enzymes. J. Appl. Bot. 73 (1999) 184-190
29. Pflugmacher S., Wiegand C., Beattle K.A., Krause E., Steinberg C.E.W., and Codd G.A. Uptake, effects and metabolism of cyanobacterial toxins in the emergent reed plant Phragmites australis (Cav.). Trin. Ex. Steud. Environ. Toxic. Chem. 20 4 (2000) 846-852
30. Pflugmacher S. Possible allelopathic effects of cyanotoxins, with reference to Microcystin LR, in aquatic ecosystems. Wiley Period, Inc. Environ. Toxicol. 17 (2002) 407-413
31. Pflugmacher S., Tidwell L.F., and Steinberg C.E.W. Dissolved humic substances directly affect freshwater organisms. Acta Hydrochim. Hydrobiol. 29 (2001) 34-40
32. Pflugmacher S., Pietsch C., Reiger W., Paul A., Preuer T., Zwirnmann E., and Steinberg C.E.W. Humic substances and their direct effects on the physiology of aquatic plants. In: Ghabbour E.A., and Davies G. (Eds). Humic Substances: Nature's Most Versatile Materials (2003), Taylor & Francis, New York
33. Pflugmacher S. Promotion of oxidative stress in the aquatic macrophyte Ceratophyllum demersum during biotransformation of the cyanobacterial toxin microcystin-LR. Aquat. Toxicol. 70 (2004) 169-178
34. Polunin N.V.C. The decomposition of emergent macrophytes in freshwater. Adv. Ecol. Res. 14 (1984) 115-166
35. Price A.H., Atherton N.M., and Hendry G.A.F. Plants under drought-stress generate activated oxygen. Free Radical Res. Commun. 8 (1989) 61-66
36. Rice-Evans C.A., Miller N.J., Bolwell P.G., Bramley P.M., and Pridham J.B. The relative antioxidant activities of plant-derived polyphenolic flavonoids. Free Radical Res. 22 (1995) 375-383
37. Riipi M., Ossipov V., Lempa K., Haukioja E., Koricheva J., Ossipova S., and Pihlaja K. Seasonal changes in birch leaf chemistry: are there trade-offs between leaf growth and accumulation of phenolics. Oecologia 130 (2002) 380-390
38. Salminen J., Roslin T., Karonen M., Sinkkonen J., Pihlaja K., and Pulkkinen P. Seasonal variation in the content of hydrolizable tannins, flavonoid glycosides and proanthocyanidins in oak leaves. J. Chem. Ecol. 30 9 (2004) 1693-1711
39. Scalbert A., and Haslam E. Plant polyphenols and chemical defense. Part 2: Polyphenols and chemical defense of the leaves of Quercus robur. Phytochemistry 26 (1987) 3191-3195
40. Scalbert A., Monties B., and Favre J.M. Polyphenols of Quercus robur: adult tree and in vitro grown calli and shoots. Phytochemistry 27 (1988) 3483-3488
41. Sersen F., Kralova K., and Bumbalova A. Action of mercury on the photosynthetic apparatus of spinach chloroplasts. Photosynthetica 35 (1998) 551-559
42. Wetzel R.G. Death, detritus and energy flow in aquatic ecosystems. Freshwater Biol. 33 (1995) 83-89
43. Wetzel R.G. Limnology: lake and river ecosystems. third ed. (2001), Academic Press, San Diego pp. 527-664
44. Yang Y., Sharma R., Sharma A., Awasthi S., and Awasthi Y.C. Lipid peroxidation and cell cycle signaling: 4-hydroxynonenal, a key molecule in stress mediated signaling. Acta Biochim. Polon. 50 2 (2003) 319-336
45. Zhu Y.L., Philon-Smits E.A.H., Tarun A.S., Weber S.U., Jouanin L., and Terry N. Cadmium tolerance and accumulation in Indian mustard is enhanced by overexpressing gamma-glutamylcysteine synthetase. Plant Physiol. 121 (1999) 1169-1178