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Submersed macrophyte growth at low pH

II. CO2 × sediment interactions

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Abstract

The submersed macrophyte Vallisneria americana was grown for seven weeks in a greenhouse to test for differences in the ability of three different sediments to support growth stimulation in response to CO2 enrichment at low pH. Plants accumulated 21- to 24-fold greater biomass at 10 × ambient CO2 concentrations than at ambient CO2 on all sediments. At both CO2 levels, plants grown on sediment from an acidified lake accumulated ca. 81%, and those grown on oligotrophic lake sediment ca. 47% as much biomass as plants grown on alkaline lake sediment. Despite striking CO2 and sediment effects on biomass accumulation, there was no significant interaction (using log-transformed data) between CO2 and sediment effects, indicating that all sediments allowed similar proportionate growth responses to CO2 enrichment. Plants grown on the less fertile sediments showed greater relative allocation to horizontal versus vertical growth by producing more rosette-bearing stolons in relation to plant height (leaf length) than plants grown on relatively fertile, alkaline lake sediment. Tissue analysis suggested that sediment effects on Vallisneria growth could be attributed neither to mineral putrient (nitrogen and phosphorus) limitation nor to aluminum toxicity in these low pH treatments. In any case, CO2 availability can be an important regulator of submersed macrophyte growth at low pH on a variety of sediment types, including those from oligotrophic and acidic lakes.

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References

  • Allen SE, Grimshaw HM, Rowland AP (1986) Chemical analysis, In: Moore PD, Chapman (eds) Methods in Plant Ecology, 2nd ed. Blackwell Scientific, Oxford, pp 285–344

    Google Scholar 

  • Barko JW, Smart RM (1986) Sediment-related mechanisms of growth limitation in submersed macrophytes. Ecology 67:1328–1340

    Google Scholar 

  • Barko JB, Smart RM, McFarland DG (1991) Interactive effects of environmental conditions on the growth of submersed aquatic macrophytes. J Freshwater Ecol 6:199–207

    Google Scholar 

  • Carignan R (1984) Interstitial water sampling by dialysis: methodological notes. Limnol Oceanogr 29:667–670

    Google Scholar 

  • Chapin FS III, Bloom AJ, Field CB, Waring RH (1987) Plant responses to multiple environmental factors. BioScience 37:49–57

    Google Scholar 

  • Charles DF (1984) Recent pH history of Big Moose Lake (Adirondack Mountains, New York, USA) inferred from sediment diatom assemblages. Verh Internat Verein Limnol 22:559–566

    Google Scholar 

  • Colquhoun J, Kretser W, Pfeiffer M (1984) Acidity status update of lakes and streams in New York state. New York State Department of Environmental Conservation, p 140

  • Coleman JS, Rochefort L, Bazzaz FA, Woodward FI (1991) Atmospheric CO2, plant nitrogen status and the susceptibility of plants to an acute increase in temperature. Plant Cell Environment 14:667–674

    Google Scholar 

  • Conroy JP, Milham PJ, Mazur M, Barlow EWR (1990) Growth, dry weight partitioning and wood properties of Pinus radiata D. Don after 2 years of CO2 enrichment. Plant Cell Environment 13:329–337

    Google Scholar 

  • Crow GE, Hellquist CB (1982) Aquatic vascular plants of New England: Part 4 Juncaginaceae, Scheuchzeriaceae, Butomaceae, Hydrocharitaceae. New Hampshire AG Exp Sta Bull 520

  • Cure JD, Acock B (1986) Crop responses to carbon dioxide doubling: a literature survey. Agricult For Meteorol 38:127–145

    Google Scholar 

  • Farmer AM (1990) The effects of lake acidification on aquatic macrophytes—a review. Environ Pollut 65:219–240

    Google Scholar 

  • Field C, Mooney HA (1986) The photosynthesis-nitrogen relationship in wild plants. In: T.J. Givnish (ed) On the economy of plant form and function, Cambridge University Press, Cambridge, England, pp 25–55

    Google Scholar 

  • Gerloff, GC (1975) Nutritional ecology of nuisance aquatic plants. National Environmental Research Center, Office of Research and Development, U.S. Environmental Protection Agency, Corvallis, OR, USA 97330

    Google Scholar 

  • Gerloff GC, Krombholz PH (1966) Tissue analysis as a measure of nutrient availability for the growth of angiosperm aquatic plants. Limnol Oceanogr 11:529–537

    Google Scholar 

  • Grisé D, Titus JE, Wagner DJ (1986) Enirnmental pH influences growth and tissue chemistry of the submersed macrophyte Vallisneria americana. Can J Bot 64:306–310

    Google Scholar 

  • Harman WN, Sohacki LP (1980) The limnology of Otsego Lake (Glimmerglass). In: Bloomfield, JA (ed) Lakes of New York State, vol. 3. Ecology of the lakes of east-central New York. Academic Press, New York, pp 1–128

    Google Scholar 

  • Havilah EJ, Wallis DM, Morris R, Woolnough JA (1977) A microcolourimetric method for determination of ammonia in Kjeldahl digests with a manual spectrophometer. Lab Pract 26:545–547

    Google Scholar 

  • Hesslein RH (1976) An in situ sampler for close interval porewater studies. Limnol Oceanogr 21:912–914

    Google Scholar 

  • Hocking PJ, Meyer CP (1985) Responses of Noogoora burr (Xanthium occidentale Bertol.) to nitrogen supply and carbon dioxide enrichment. Ann Bot 55:835–844

    Google Scholar 

  • Hutchinson GE (1975) A treatise on limnology, vol. 3. Limnological botany. John Wiley and Sons, New York, p 660

    Google Scholar 

  • James BR, Clark CJ, Riha SJ (1983) An 8-hydroxyquinoline method for labile and total aluminum in soil extracts. Soil Sci Soc Am J 47:893–897

    Google Scholar 

  • Kelly CA, Rudd JWM, Furutani A, Schindler DW (1984) Effects of lake acidification on rates of organic matter decomposition in sediments. Limnol Oceanogr 29:687–694

    Google Scholar 

  • Larigauderie A, Hilbert DW, Oechel WC (1988) Effect of CO2 enrichment and nitrogen availability on resource acquisition and resource allocation in a grass, Bromus mollis. Oecologia 77:544–549

    Google Scholar 

  • Lincoln DE, Couvet D, Sionit N (1986) Response of an insect herbivore to host plants grown in carbon dioxide enriched atmospheres. Oecologia 69:556–560

    Google Scholar 

  • Murphy J, Riley JP (1962) A modified single solution method for the determination of phosphate in natural waters. Anal Chim Acta 27:31–36

    Google Scholar 

  • Norby RJ, O'Neill EG, Luxmoore RJ (1986) Effects of atmospheric CO2 enrichment on the growth and mineral nutrition of Quercus alba seedlings in nutrient-poor soil. Plant Physiol 82:83–89

    Google Scholar 

  • Overath RD, Titus JE, Hoover DT, Grisé DG (1991) The influence of field site and natural sediments on the growth and tissue chemistry of Vallisneria americana Michx. J Freshwater Ecol 6:135–145

    Google Scholar 

  • Roelofs JGM, Schuurkes JAAR, Smits AJM (1984) Impact of acidification and eutrophication on macrophyte communities in softwaters. II. Experimental studies. Aquat Bot 18:389–411

    Google Scholar 

  • Rorison IH (1980) The effects of soil acidity on nutrient availability and plant response. In: Hutchinson TC, Havas T (eds) Effects of Acid Precipitation on Terrestrial Ecosystems, Plenum Press, New York, pp 283–304

    Google Scholar 

  • SAS Institute Inc (1985) SAS User's Guide: Statistics, Version 5 Edition. SAS Institute, Cary, North Carolina, USA, p 956

    Google Scholar 

  • Sculthorpe CD (1967) The biology of aquatic vascular plants. Edward Arnold Publishers, London, p 610

    Google Scholar 

  • Slade AJ, Hutchings MJ (1987) The effects of nutrient availability on foraging in the clonal herb Glechoma hederacea. J Ecol 75:93–112

    Google Scholar 

  • Smart RM, Barko JW (1985) Laboratory culture of submersed freshwater macrophytes on natural sediments. Aquat Bot 21:251–263

    Google Scholar 

  • Stumm W, Morgan JJ (1970) Aquatic Chemistry: An Introduction Emphasizing Chemical Equilibria in Natural Waters. Wiley-Interscience, NY

    Google Scholar 

  • Taylor BR, Parkinson D, Parsons WFJ (1989) Nitrogen and litter content as predictors of litter decay rates: a microcosm test. Ecology 70:97–104

    Google Scholar 

  • Titus JE (in review) Carbon dioxide enrichment at low pH enhances nutrient accumulation in submersed macrophyte shoots

  • Titus JE, Stephens MD (1983) Neighbor influences and seasonal growth patterns for Vallisneria americana in a mesotrophic lake. Oecologia 56:23–29

    Google Scholar 

  • Titus JE, Feldman RS, Grisé D (1990) Submersed macrophyte growth at low pH. I. CO2 enrichment effects with fertile sediment. Oecologia 84:307–313

    Google Scholar 

  • Wetzel RG, Brammer ES, Lindström K, Forsberg C (1985) Photosynthesis of submersed macrophytes in acidified lakes II. Carbon limitation and utilization of benthic CO2 sources. Aquat Bot 22:107–120

    Google Scholar 

  • Wetzel RG, Grace JB (1983) Aquatic plant communities. In: Lemon ER (ed) CO2 and Plants: the Response of Plants to Rising Levels of Atmospheric Carbon Dioxide, AAAS Selected Symposium 84, Westview Press Inc, Boulder, pp 223–280

    Google Scholar 

  • Wong SL (1979) Elevated atmospheric partial pressure of CO2 and plant growth. I. Interactions of nitrogen nutrition and photosynthetic capacity in C3 and C4 plants. Oecologia 44:68–74

    Google Scholar 

  • Yan ND, Miller GE, Wile I, Hitchin GG (1985) Richness of aquatic macrophyte floras of soft water lakes of differing pH and trace metal content in Ontario, Canada. Aquat Bot 23:27–40

    Google Scholar 

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  1. Department of Biological Sciences, State University of New York, 13902, Binghamton, NY, USA

    John E. Titus

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Titus, J.E. Submersed macrophyte growth at low pH. Oecologia 92, 391–398 (1992). https://doi.org/10.1007/BF00317465

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  • DOI: https://doi.org/10.1007/BF00317465

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