Skip to main content
Log in

Community interactions between the filamentous alga Cladophora glomerata (L.) Kuetzing, its epiphytes, and epiphyte grazers

  • Original Papers
  • Published:
Oecologia Aims and scope Submit manuscript

Summary

Interactions between epiphytes, epiphyte grazers and the filamentous green alga Cladophora glomerata (L.) Kuetzing were explored with smaples from rivers in Montana. Extracts of C. glomerata lowered photosynthetic rates of Nitzschia fonticola Grunow (an epiphytic diatom). Nutrient enrichment showed that C. glomerata from the Madison River was N deficient and its epiphytes were P deficient on 2 dates and N deficient on one date, while no nutrient deficiencies were detected in samples from 3 other rivers; this implies there was little nutrient competition between the epiphytes and C. glomerata. Epiphytes lowered drag on C. glomerata tufts and current velocity inside the tufts, apparently by decreasing the effective surface area. Lower drag may decrease detachment, but lowering current velocity from 8 to 0 cm s-1 resulted in a 100 % decrease in photosynthesis. Light absorption by epiphyte pigments may lower photosynthetic rate of C. glomerata when irradiance is below 200–500 μE m-2 s-1, and protect against photoinhibition above this irradiance range. Invertebrate grazers (predominantly Baetis tricaudatus Dodds, Trycorythodes minutus Traver and Brachycentrus occidentalis Banks) at high densities removed 75% of epiphytes and B. occidentalis grazed on C. glomerata. Invertebrates regenerated a mean of 0.16 μmol NH sup+inf4 individual-1 d-1 which could have enhanced growth of downstream C. glomerata. Competition and grazing were not the only interactions in the C. glomerata community, positive (mutualistic) interactions were also important.

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

  • Atsatt PR, O'Dowd DJ (1976) Plant defense guilds. Science 193:24–29

    Google Scholar 

  • Bahls LL, Weber EE (1988) Ecology and distribution in Montana of Epithemia Sorex Kutz., a common nitrogen-fixing diatom. Proc Mont Acad Sci 48:15–20

    Google Scholar 

  • Black R, Peterson CH (1987) Biological vs. physical explanations for the non-random pattern of host occupation by a macroalga attaching to infaunal biovalve molluscs. Oecologia 73:213–221

    Google Scholar 

  • Blum JL (1956) The ecology of river algae. Bot Rev 22:291–341

    Google Scholar 

  • Boucher DH, James S, Keeler KH (1982) The ecology of mutualism. Ann Rev Ecol Sys 13:315–347

    Google Scholar 

  • Carpenter SR, Kitchell JF (1988) Consumer control of lake productivity. Bio Sci 38:764–769

    Google Scholar 

  • Dodds WK (1988) Community structure and selection for positive or negative species interactions. Oikos 53:387–390

    Google Scholar 

  • Dodds WK (1989a) Microscale vertical profiles of N2 fixation, photosynthesis, O2, chlorophyll a, and light in a cyanobacterial assemblage. Appl Environ Microbiol 55:882–886

    Google Scholar 

  • Dodds WK (1989b) Photosynthesis of different morphologies of Nostoc parmelioides (cyanobacteria) as related to current velocities and diffusion patterns. J Phycol 25:258–262

    Google Scholar 

  • Dodds WK (1990) Hydrodynamic constraints of evolution of chemically mediated interactions between aquatic organisms in unidirectional flows. J Chem Ecol 16:1417–1430

    Google Scholar 

  • Dodds WK, Castenholz RW (1988) Effects of grazing and season on the growth of Nostoc pruniforme. Br J Phycol 23:219–227

    Google Scholar 

  • Dodds WK, Johnson KR, Priscu JC (1989) Simultaneous nitrogen and phosphorus deficiency in natural phytoplankton assemblages: theory, empirical evidence, and implications for lake management. Lake Res Man 5:21–26

    Google Scholar 

  • Dodds WK, Priscu JC (1990) The influence of phosphate enrichment on ammonium and nitrate flux in an oligotrophic lake: mesocosm studies. Hydrobiologia (in press)

  • Dudley TL, Cooper SD, Hemphill W (1986) Effects of macroalgae on a stream invertebrate community. J N Am Benthol Soc 5:93–106

    Google Scholar 

  • Duffy JE (1990) Amphipods on seaweeds: partners or pests? Oecologia 83:267–276

    Google Scholar 

  • Fairchild JF, Boyle T, English WR, Raben C (1987) Effects of sediment and contaminated sediment on structural and functional components of experimental stream ecosystems Water Air Soil Poll 36:271–293

    Google Scholar 

  • Filbin GJ, Hough R (1984) Extraction of 14C-labeled photosynthate from aquatic plants with dimethyl sulfoxide (DMSO). Limnol Oceanogr 29(2):426–428

    Google Scholar 

  • Fitzgerald GP (1969) Some factors in the competition or antagonism around bacteria, algae and aquatic weeds. J Phycol 5:351–359

    Google Scholar 

  • Graham JM, Aver MT, Canale RP, Hoffmann JP (1982) Ecological studies and mathematical modeling of Cladophora in Lake Huron: 4. Photosynthesis and respiration as functions of light and temperature. J Great Lakes Res 8:100–111

    Google Scholar 

  • Gray LJ, Ward JV (1979) Food habits of stream benthos at sites of differing food availability. Am Mid Nat 102:157–167

    Google Scholar 

  • Greger PD, Deacon JE (1988) Food partitioning among fishes of the Virgin River. Copeia 1988(2):314–323

    Google Scholar 

  • Harrison PG (1982) Control of microbial growth and of amphipod grazing by water-soluble compounds from leaves of Zostera marina. Mar Biol 67:225–230

    Google Scholar 

  • Harrison PG, Durance CD (1985) Reductions in photosynthetic carbon uptake in epiphytic diatoms by water soluble extracts of leaves of Zostera marina. Mar Biol 90:117–119

    Google Scholar 

  • Hay ME, Fenical W, Gustafson K (1989) Chemical defense against diverse coral-reef herbivores. Ecology 68:1581–1591

    Google Scholar 

  • Hay ME, Pawlik JR, Duffy JE, Fenical W (1989) Seaweed-herbivore predator interactions: host-plant specialization reduces predation on small herbivores. Oecologia 81:418–427

    Google Scholar 

  • Holomuzki JR, Short TM (1988) Habitat use and fish avoidance behaviors by the stream-dwelling isopod Liricus fontinalis. Oikos 52:79–86

    Google Scholar 

  • LaBarbera M, Vogel S (1976) An inexpensive thermistor flow meter for aquatic biology. Limnol Oceanogr 21:750–756

    Google Scholar 

  • Marcus JH, Sutcliffe DW, Willoughby LG (1978) Feeding and growth of Assellus aquaticus (Isopoda) on food items from the littoral of Windermere, including green leaves of Elodia canadensis. Freshw Biol 8:505–519

    Google Scholar 

  • Nowell ARM, Jumars PA (1984) Flow environments of aquatic benthos. Ann Rev Ecol Syst 15:308–328

    Google Scholar 

  • Orth RJ, van Montfrans J (1984) Epiphyte-seagrass relationships with an emphasis on the role of micrograzing: a review. Aquat Bot:18:43–69

    Google Scholar 

  • Parsons TR, Maita Y, Lalli CM (1984) A Manual of Chemical and Biological Methods for Seawater Analysis. Permagon Press, Oxford

    Google Scholar 

  • Patrick R, Rhyne CF, Richardson RW III, Larson RA, Bott TT, Rogenmuser K (1983) The potential for biological controls of Cladophora glomerata. EPA 600/3-83-065

  • Platt T, Gallegos CL, Harrison WG (1980) Photoinhibition of photosynthesis in natural assemblages of marine phytoplankton. J Mar Res 38(4):687–701

    Google Scholar 

  • Power ME (1990) Benthic tufts versus floating mats of algae in river food webs. Oikos 58:67–80

    Google Scholar 

  • Priscu JC (1989) Photon dependence of inorganic nitrogen transport by phytoplankton in perennially ice-covered antarctic lakes. Hydrobiologia 172:173–182

    Google Scholar 

  • Sand-Jensen K (1977) Effect of epiphytes on eelgrass photosynthesis. Aquat Bot 3:55–63

    Google Scholar 

  • Sand-Jensen K, Borum J (1984) Epiphyte shading and its effect on photosynthesis and diel metabolism of Lobellia dortmanna L. during the spring bloom in a Danish lake. Aquat Bot 20:109–119

    Google Scholar 

  • Schmitt RJ (1987) Indirect interactions between prey: apparent competition, predator aggregation, and habitat segregation. Ecology 68:1887–1897

    Google Scholar 

  • Solorzano L (1969) Determination of ammonia in natural waters by the phenolhypochlorite method. Limnol Oceanogr 14:799–801

    Google Scholar 

  • Vogel S (1981) Life in moving fluids. Princeton University Press, Princeton, New Jersey

    Google Scholar 

  • Waaland SD, Waaland JR (1975) Analysis of cell elongation in red alage by fluorescent labelling. Planta (Berl) 126:127–138

    Google Scholar 

  • Wheeler WN (1980) Effect of boundary layer transport on the fixation of carbon by the giant kelp Macrocystis pyrifera. Mar Biol 56:103–110

    Google Scholar 

  • Whitton BA (1970) Biology of Cladophora in freshwaters. Water Res 4:457–476

    Google Scholar 

  • Wium-Andersen S, Antoni V, Christophersen C, Hoven G (1982) Allelopathic effects on phytoplankton by substances isolated from aquatic macrophytes (Charales). Oikos 39:187–190

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dodds, W.K. Community interactions between the filamentous alga Cladophora glomerata (L.) Kuetzing, its epiphytes, and epiphyte grazers. Oecologia 85, 572–580 (1991). https://doi.org/10.1007/BF00323770

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00323770

Key words

Navigation