Skip to main content
Log in

Effects of Cu, Pb and Zn on two Potamogeton species grown under field conditions

  • Published:
Vegetatio Aims and scope Submit manuscript

Abstract

Two common macrophyte species, Potamogeton perfoliatus L. and Potamogeton pectinatus L. were grown for 12 weeks at shallow depths in sediments contaminated with 1250 or 2500 μg Pb or Cu and/or Zn (gDW sediment)-1. Control experiments were run at background levels of 4, 13, and 38 μg Pb, Cu and Zn (gDW sediment)-1, respectively. Effects of heavy metals on biomass production and metal uptake and distribution in plants are presented in relation to total amount and plant-available fraction of metals in the sediment.

All three studied metals gave reduced biomass production, and the toxicity of the metals decreased in the order Zn>Cu>Pb. The root/shoot biomass ratio increased for P. pectinatus, but decreased for P. perfoliatus with metal treatment. The content of any single metal was higher in shoots than in roots of plants grown on sediments not contaminated with that specific metal, but addition of that metal increased the proportion in roots. The uptake by plants of any of the heavy metals increased with increased metal addition. The magnitude of the plant-available fraction of metals of untreated sediment was Zn>Cu>Pb, and increased in contaminated sediments. Addition of Cu decreased both the plant-available fraction and the total concentration of Zn in the sediment, while increased the uptake of Zn by the plants. The opposite was found for Cu when Zn was added. P. pectinatus accumulated about twice as much Cu as P. perfoliatus. On the other hand, the concentration of Pb was higher in P. perfoliatus than in P. pectinatus, and was negligible in P. pectinatus when cultivated in untreated sediments.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Agami, M. & Waisel, Y. 1986. The ecophysiology of submerged vascular plants. Physiol. Veg. 24: 607–624.

    Google Scholar 

  • Andersson, A. 1976. On the determination of ecologically significant fractions of some heavy metals in soil. Swedish J. agric. Res. 6: 19–25.

    Google Scholar 

  • Barko, J. W. & Smart, R. M. 1980. Mobilization of sediment phosphorus by submersed freshwater macrophytes. Freshwater Biol. 10: 229–238.

    Google Scholar 

  • Barko, J. W. & Smart, R. M. 1981. Comparative influences of light and temperature on the growth and metabolism of selected submerged freshwater macrophytes. Ecol. Monogr. 51: 219–235.

    Google Scholar 

  • Barko, J. W., Adams, M. S. & Clesceri, N. L., 1986. Environmental factors and their consideration in the management of submersed aquatic vegetation: a review. J. Aquat. Plant Manage. 24: 1–10.

    Google Scholar 

  • Best, M. D. & Mantai, K. E., 1978. Growth of Myriophyllum: sediment or lake water as the source of nitrogen and phosphorus. Ecol. 59: 1075–1080.

    Google Scholar 

  • Bazzaz, F. A., Carson, R. W. & Rolfe, G. L. 1974. The effect of heavy metals on plants: Part I. Inhibition of gas exchange in sunflower by Pb, Cd, Ni and Tl. Environ. Pollut. 7: 241–246.

    Google Scholar 

  • Carignan, R. & Kalff, J. 1980. Phosphorus sources for aquatic weeds: water or sediments? Science 207: 987–989.

    Google Scholar 

  • Collinson, C. & Shimp, N. F. 1972. Trace elements in bottom sediments from Upper Peoria Lake, Middle Illinois River—a pilot project. Ill. St. Geol. Survey environ, Geol. Notes No 56.21

  • Coughtrey, P. J. & Martin, M. H. 1978. Cadmium uptake and distribution in tolerant and non-tolerant populations of Holcus lanatus grown in solution culture. Oikos 30: 555–560.

    Google Scholar 

  • Cushing, C. E. & Thomas, J. M. 1980. Cu and Zn kinetics in Myriophyllum heterophyllum Michx. and Potamogeton richardsonii (ar. Benn.) Rydb. Ecol. 61: 1321–1326.

    Google Scholar 

  • Diks, D. M. & Allen, H. E. 1983. Correlation of copper distribution in a freshwater-sediment system to bioavailability. Bull. Environ. Cont. Tox. 30: 37–43.

    Google Scholar 

  • Fabris, G. J., Harris, J. E. & Smith, I. D. 1982. Uptake of cadmium by the seagrass Heterozostera tasmanica from Corio Bay and Western Port, Victoria. Aust. J. Mar. Freshw. Res. 33: 829–836.

    Google Scholar 

  • Greger, M. & Lindberg, S. 1987. Effects of Cd2+ and EDTA on young sugar beets (Beta vulgaris). II. Net uptake and distribution of Mg2+, Ca2+ and Fe2+/Fe3+. Physiol. Plant. 69: 81–86.

    Google Scholar 

  • Greger, M., Brammer, E. S., Lindberg, S., Larsson, G. & Idestam-Almquist, J. 1991. Uptake and physiological effects of cadmium in sugar beet Beta vulgaris related to mineral provision. J. Exp Bot. 42: 729–737.

    Google Scholar 

  • Greger, M. & Ögren, E. 1991. Direct and indirect effects of Cd2+ on photosynthesis in sugar beet (Beta vulgaris). Physiol. Plant. 83: 129–135.

    Google Scholar 

  • Greger, M. & Bertell, G. 1992. Effects of Ca2+ and Cd2+ on the carbohydrate metabolism in sugar beet (Beta vulgaris). J. Exp. Bot. 43: (in press).

  • Guilizzoni, P., Adams, M. S. & MacGaffey, N. 1984. The effects of chromium on growth and photosynthesis of a submersed macrophyte, Myriophyllum spicatum. Ecol. Bull. 36: 90–96.

    Google Scholar 

  • Hampp, R., Beulich, K. & Ziegler, H. 1976. Effects of zinc and cadmium on photosynthesis, CO2-fixation and Hill activity of isolated spinach chloroplasts. Z. Pflanzen. 77: 336–344.

    Google Scholar 

  • Harding, J. P. C. & Whitton, B. A. 1978. Zinc, cadmium and lead in water, sediment and submerged plants of the Derwent reservoir, Northern England. Water Res. 12: 307–316.

    Google Scholar 

  • Jarvis, S. C., Jones, L. H. P. & Hopper, M. J. 1976. Cadmium uptake from solution by plants and its transport from roots to shoots. Plant and Soil 44: 179–191.

    Google Scholar 

  • Kautsky, L. 1991. In situ experiments of competitive relationship between six Baltic macrophyte species. Aquat. Bot. 39: 159–172.

    Google Scholar 

  • Lyngby, J. E., Brix, H. & Schierup, H.-H. 1982. Absorption and translocation of zinc in eelgrass (Zostera marina L.). J. Exp. Mar. Biol. Ecol. 58: 259–270.

    Google Scholar 

  • Mayes, R. A., McIntosh, A. W. & Andersen, V. L. 1977. Uptake of cadmium and lead by a rooted aquatic macrophyte (Elodea canadensis). Ecol. 58: 1176–1180.

    Google Scholar 

  • McIntosh, A. W., Shephard, B. K., Mayers, R. A., Atchison, G. J. & Nelson, D. W. 1978. Some aspects of sediments distribution and macrophyte cycling of heavy metals in a contaminated lake. J. Environ. Qual. 7: 301–305.

    Google Scholar 

  • Nichols, D. S. & Keeney, D. R. 1976a. Nitrogen nutrition of Myriophyllum spicatum: variation of plant tissue nitrogen concentration with season and site in Lake Wingra. Freshwater Biol. 6: 137–144.

    Google Scholar 

  • Nichols, D. S. & Keeney, D. R. 1976b. Nitrogen nutrition of Myriophyllum spicatum: uptake and translocation of N by shoots and roots. Freshwater Biol. 6: 137–144.

    Google Scholar 

  • Page, A. L., Bingham, F. T. & Nelson, C. 1972. Cadmium absorption and growth of various plant species as influenced by solution cadmium concentration. J. Environ. Qual. 1: 288–291.

    Google Scholar 

  • Pita, F. W. & Hyne, N. J. 1975. The depositional environment of zinc, lead and cadmium in reservoir sediments. Water Res. 9: 701–706.

    Google Scholar 

  • Roelofs, J. G. M., Schuurkes, J. A. A. R. & Smits, A. J. M. 1984. Impact of acidification and eutrophication on macrophyte communities in soft waters. II. Experimental studies. Aquatic. Bot. 18: 389–411.

    Google Scholar 

  • Root, R. A., Miller, R. J. & Koeppe, D. E. 1975. Uptake of cadmium — its toxicity, and effect on the iron ratio in hydroponically grown corn. J. Environ. Qual. 4: 473–476.

    Google Scholar 

  • Schlegel, H., Godbold, D. L. & Hüttermann, A. 1987. Whole plant aspects of heavy metal induced changes in CO2 uptake and water relations of spruce (Picea abies) seedlings. Physiol. Plant. 69: 265–270.

    Google Scholar 

  • Shimp, N. F., Leland, H. V. & White, W. A. 1970. Distribution of major, minor and trace constituents in unconsolidated sediments of southern Lake Michigan. Ill. St. Geol. Survey environ. Geol. Notes 32. 19.

    Google Scholar 

  • Suckcharoen, S. 1979. Ceratophyllum demersum as an indicator of mercury contamination in Thailand and Finland. Ann. Bot. Fenn. 16: 173–175.

    Google Scholar 

  • Taylor, G. J. & Crowder, A. A. 1982. Uptake and accumulation of copper, nickel and iron by Typha latifolia grown in solution culture. Can. J. Bot. 61: 1825–1830.

    Google Scholar 

  • Thursby, G. B. 1984. Root-exudated oxygen in the aquatic angiosperm Ruppia maritima. Mar. Ecol. Prog. Ser. 16: 303–305.

    Google Scholar 

  • Welsh, R. P. H. & Denny, P. 1980. The uptake of lead and copper by submerged aquatic macrophytes in two english lakes. J. Ecol. 68: 443–455.

    Google Scholar 

  • Wiederholm, T., Wiederholm, A. & Milbrink, G. 1987. Bulk sediment bioassays with five species of freshwater oligochaetes. Water, Air, Soil Pollut. 36: 131–154.

    Google Scholar 

  • Wium-Andersen, S. & Andersen, J. M. 1972. Carbon dioxide content of the interstitial water in the sediment of Grane Langso, A Danish Lobelia lake. Limnol. Ocean. 17: 943–947.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Greger, M., Kautsky, L. Effects of Cu, Pb and Zn on two Potamogeton species grown under field conditions. Vegetatio 97, 173–184 (1991). https://doi.org/10.1007/BF00035390

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00035390

Keywords

Navigation