Skip to main content Accessibility help
×
Hostname: page-component-76fb5796d-9pm4c Total loading time: 0 Render date: 2024-04-28T16:25:56.475Z Has data issue: false hasContentIssue false

17 - The role of fungi in carbon and nitrogen cycles in freshwater ecosystems

Published online by Cambridge University Press:  10 December 2009

Vladislav Gulis
Affiliation:
Department of Biological Sciences, University of Alabama Tuscaloosa, AL 35487, USA
Kevin Kuehn
Affiliation:
Department of Biology, Eastern Michigan University, Ypsilanti MI, USA
Keller Suberkropp
Affiliation:
Department of Biological Sciences, University of Alabama Tuscaloosa, AL 35487, USA
Geoffrey Michael Gadd
Affiliation:
University of Dundee
Get access

Summary

Introduction

Fungi are adapted to a diverse array of freshwater ecosystems. In streams and rivers, flowing water provides a mechanism for downstream dispersal of fungal propagules. The dominant group of fungi in these habitats, aquatic hyphomycetes, have conidia that are morphologically adapted (tetraradiate and sigmoid) for attachment to their substrates (leaf litter and woody debris from riparian vegetation) in flowing water (Webster, 1959; Webster & Davey, 1984). In freshwater wetlands and lake littoral zones, production of emergent aquatic macrophytes is often extremely high, resulting in an abundance of plant material that eventually enters the detrital pool. The dead shoot material of these macrophytes (leaf blades, leaf sheaths and culms) often remains standing for long periods of time before collapsing to the sediments or water. This plant matter is colonized by fungi that are adapted for surviving the harsh conditions that prevail in the standing-dead environment (Kuehn et al., 1998). There are a number of other freshwater ecosystems where fungi are present and exhibit interesting adaptations, e.g. aero-aquatic fungi in woodland ponds, zoosporic organisms (Chytridiomycota and Oomycota) in a variety of habitats including the pelagic zones of lakes, and Trichomycetes that inhabit the guts of a variety of aquatic insects. Despite the well-known occurrence of these fungal groups in aquatic habitats, virtually nothing is known concerning their roles in biogeochemical processes. Overall, the contributions of fungi to biogeochemical cycles have been understudied in most freshwater ecosystems.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2006

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Allan, J. D. (1995). Stream ecology: Structure and Function of Running Waters. London: Chapman & Hall.CrossRefGoogle Scholar
Arsuffi, T. L. & Suberkropp, K. (1986). Growth of two stream caddisflies (Trichoptera) on leaves colonized by different fungal species. Journal of the North American Benthological Society, 5, 297–305.CrossRefGoogle Scholar
Baldy, V. & Gessner, M. O. (1997). Towards a budget of leaf litter decomposition in a first-order woodland stream. Comptes Rendus de l'Academie des Sciences – Series III – Sciences de la Vie, 320, 747–58.CrossRefGoogle Scholar
Baldy, V., Gessner, M. O. & Chauvet, E. (1995). Bacteria, fungi and the breakdown of leaf litter in a large river. Oikos, 74, 93–102.CrossRefGoogle Scholar
Baldy, V., Chauvet, E., Charcosset, J. Y. & Gessner, M. O. (2002). Microbial dynamics associated with leaves decomposing in the mainstem and floodplain pond of a large river. Aquatic Microbial Ecology, 28, 25–36.CrossRefGoogle Scholar
Bärlocher, F. (1985). The role of fungi in the nutrition of stream invertebrates. Botanical Journal of the Linnaean Society, 91, 83–94.CrossRefGoogle Scholar
Bärlocher, F. (2000). Water-borne conidia of aquatic hyphomycetes: seasonal and yearly patterns in Catamaran Brook, New Brunswick, Canada. Canadian Journal of Botany, 78, 157–67.CrossRefGoogle Scholar
Bärlocher, F. & Biddiscombe, N. R. (1996). Geratology and decomposition of Typha latifolia and Lythrum salicaria in a freshwater marsh. Archiv für Hydrobiologie, 136, 309–25.Google Scholar
Bärlocher, F. & Corkum, M. (2003). Nutrient enrichment overwhelms diversity effects in leaf decomposition by stream fungi. Oikos, 101, 247–52.CrossRefGoogle Scholar
Bärlocher, F. & Kendrick, B. (1973a). Fungi and food preferences of Gammarus pseudolimnaeus. Archiv für Hydrobiologie, 72, 501–16.Google Scholar
Bärlocher, F. & Kendrick, B. (1973b). Fungi in the diet of Gammarus pseudolimnaeus (Amphipoda). Oikos, 24, 295–300.CrossRefGoogle Scholar
Bärlocher, F. & Newell, S. Y. (1994). Growth of the saltmarsh periwinkle Littoraria irrorata on fungal and cordgrass diets. Marine Biology, 118, 109–14.CrossRefGoogle Scholar
Benner, R., Moran, M. A. & Hodson, R. E. (1986). Biochemical cycling of lignocellulosic carbon in marine and freshwater ecosystems: relative contributions of prokaryotes and eukaryotes. Limnology and Oceanography, 21, 89–100.CrossRefGoogle Scholar
Buesing, N. (2002). Microbial productivity and organic matter flow in a littoral reed stand. Unpublished Ph.D. thesis, Swiss Federal Institute of Technology, Zurich, Switzerland.
Carter, M. D. & Suberkropp, K. (2004). Respiration and annual fungal production associated with decomposing leaf litter in two streams. Freshwater Biology, 49, 1112–22.CrossRefGoogle Scholar
Chamier, A. C. (1985). Cell-wall-degrading enzymes of aquatic hyphomycetes: a review. Botanical Journal of the Linnaean Society, 91, 67–81.CrossRefGoogle Scholar
Chamier, A. C. & Dixon, P. A. (1982). Pectinases in leaf degradation by aquatic hyphomycetes: the enzymes and leaf maceration. Journal of General Microbiology, 128, 2469–83.Google Scholar
Chauvet, E. (1987). Changes in the chemical composition of alder, poplar and willow leaves during decomposition in a river. Hydrobiologia, 148, 35–44.CrossRefGoogle Scholar
Chimner, R. A., Cooper, D. J. & Parton, W. J. (2002). Modelling carbon accumulation in Rocky Mountain fens. Wetlands, 22, 100–10.CrossRefGoogle Scholar
Collier, K. J. & Smith, B. J. (2003). Corrigendum to ‘Role of wood in pumice-bed streams II: breakdown and colonization’ [For. Ecol. Manage. 177 (2003) 261–276]. Forest Ecology and Management, 181, 375–90.CrossRefGoogle Scholar
Dvorák, J. & Imhof, G. (1998). The role of animals and animal communities in wetlands. In The Production Ecology of Wetlands, ed. Westlake, D. F., Kvêt, J. & Szczepanski, A.. Cambridge: Cambridge University Press, pp. 211–318.Google Scholar
Elwood, J. W., Newbold, J. D., Trimble, A. F. & Stark, R. W. (1981). The limiting role of phosphorus in a woodland stream ecosystem: effects of P enrichment on leaf decomposition and primary producers. Ecology, 62, 146–58.CrossRefGoogle Scholar
Falih, A. M. K. & Wainwright, M. (1995). Nitrification in-vitro by a range of filamentous fungi and yeasts. Letters in Applied Microbiology, 21, 18–19.CrossRefGoogle ScholarPubMed
Findlay, S., Howe, K. & Austin, H. K. (1990). Comparison of detritus dynamics in two tidal freshwater wetlands. Ecology, 71, 288–95.CrossRefGoogle Scholar
Findlay, S. E. G., Dye, S. & Kuehn, K. A. (2002a). Microbial growth and nitrogen retention in litter of Phragmites australis compared to Typha angustifolia. Wetlands, 22, 616–25.CrossRefGoogle Scholar
Findlay, S., Tank, J., Dye, S.et al. (2002b). A cross-system comparison of bacterial and fungal biomass in detritus pools of headwater streams. Microbial Ecology, 43, 55–66.CrossRefGoogle Scholar
Fisher, S. G. & Likens, G. E. (1972). Stream ecosystem: organic energy budget. Bioscience, 22, 33–5.CrossRefGoogle Scholar
Frost, P. C., Stelzer, R. S., Lamberti, G. A. & Elser, J. J. (2002). Ecological stoichiometry of trophic interactions in the benthos: understanding the role of C:N:P ratios in lentic and lotic habitats. Journal of the North American Benthological Society, 21, 515–28.CrossRefGoogle Scholar
Fuss, C. L. & Smock, L. A. (1996). Spatial and temporal variation of microbial respiration rates in a blackwater stream. Freshwater Biology, 36, 339–49.CrossRefGoogle Scholar
Gessner, M. O. (2001). Mass loss, fungal colonisation and nutrient dynamics of Phragmites australis leaves during senescence and early decay in a standing position. Aquatic Botany, 69, 325–39.CrossRefGoogle Scholar
Gessner, M. O. & Chauvet, E. (1994). Importance of stream microfungi in controlling breakdown rates of leaf litter. Ecology, 75, 1807–17.CrossRefGoogle Scholar
Gessner, M. O. & Chauvet, E. (1997). Growth and production of aquatic hyphomycetes in decomposing leaf litter. Limnology and Oceanography, 42, 496–595.CrossRefGoogle Scholar
Gessner, M. O. & Newell, S. Y. (2002). Biomass, growth rate, and production of filamentous fungi in plant litter. In Manual of Environmental Microbiology, 2nd edn, ed. Hurst, C. J., Crawford, R. L., Knudsen, G. R., McInerney, M. J. & Stetzenbach, L. D.. Washington, DC: ASM Press, pp. 390–408.Google Scholar
Gessner, M. O. & van Ryckegem, G. (2002). Water fungi as decomposers in freshwater ecosystems. In Encyclopedia of Environmental Microbiology, ed. Bitton, G.. New York: Wiley & Sons, pp. 3353–64.Google Scholar
Gessner, M. O., Suberkropp, K. & Chauvet, E. (1997). Decomposition of plant litter by fungi in marine and freshwater ecosystems. In The Mycota, Vol. IV. Environmental and Microbial Relationships, ed. Wicklow, D. T. & Söderström, B. E.. Berlin: Springer-Verlag, pp. 303–22.Google Scholar
Graça, M. A. S., Maltby, L. & Calow, P. (1993). Importance of fungi in the diet of Gammarus pulex and Asellus aquaticus II. Effects on growth, reproduction and physiology. Oecologia, 96, 304–9.CrossRefGoogle ScholarPubMed
Graça, M. A., Newell, S. Y. & Kneib, R. T. (2000). Grazing rates of organic matter and living fungal biomass of decaying Spartina alterniflora by three species of salt-marsh invertebrates. Marine Biology, 136, 281–9.Google Scholar
Grattan, R. M. & Suberkropp, K. (2001). Effects of nutrient enrichment on yellow poplar leaf decomposition and fungal activity in streams. Journal of the North American Benthological Society, 20, 33–43.CrossRefGoogle Scholar
Guest, R. K. & Smith, D. W. (2002). A potential new role for fungi in wastewater MBR biological nitrogen reduction system. Journal of Environmental Engineering and Science, 1, 433–7.CrossRefGoogle Scholar
Gulis, V. & Suberkropp, K. (2003a). Effect of inorganic nutrients on relative contributions of fungi and bacteria to carbon flow from submerged decomposing leaf litter. Microbial Ecology, 45, 11–19.CrossRefGoogle Scholar
Gulis, V. & Suberkropp, K. (2003b). Interactions between stream fungi and bacteria associated with decomposing leaf litter at different levels of nutrient availability. Aquatic Microbial Ecology, 30 149–57.CrossRefGoogle Scholar
Gulis, V. & Suberkropp, K. (2003c). Leaf litter decomposition and microbial activity in nutrient-enriched and unaltered reaches of a headwater stream. Freshwater Biology, 48, 123–34.CrossRefGoogle Scholar
Gulis, V. & Suberkropp, K. (2004). Effects of whole-stream nutrient enrichment on the concentration and abundance of aquatic hyphomycete conidia in transport. Mycologia, 96, 57–65.CrossRefGoogle ScholarPubMed
Gulis, V., Rosemond, A. D., Suberkropp, K., Weyers, H. S. & Benstead, J. P. (2004). Effects of nutrient enrichment on the decomposition of wood and associated microbial activity in streams. Freshwater Biology, 49, 1437–47.CrossRefGoogle Scholar
Gunasekera, S. A., Webster, J. & Legg, C. J. (1983). Effect of nitrate and phosphate on weight losses of pine and oak wood caused by aquatic and aero-aquatic hyphomycetes. Transactions of the British Mycological Society, 80, 507–14.CrossRefGoogle Scholar
Hamilton, S. K., Tank, J. L., Raikow, D. F.et al. (2001). Nitrogen uptake and transformation in a midwestern US stream: a stable isotope enrichment study. Biogeochemistry, 54, 297–340.CrossRefGoogle Scholar
Hieber, M. & Gessner, M. O. (2002). Contribution of stream detritivores, fungi, and bacteria to leaf breakdown based on biomass estimates. Ecology, 83, 1026–38.CrossRefGoogle Scholar
Högberg, M. N. & Högberg, P. (2002). Extramatrical ectomycorrhizal mycelium contributes one-third of microbial biomass and produces, together with associated roots, half the dissolved organic carbon in a forest soil. New Phytologist, 154, 791–5.CrossRefGoogle Scholar
Huryn, A. D., Butz Huryn, V. M., Arbuckle, C. J. & Tsomides, L. (2002). Catchment land-use, macroinvertebrates and detritus processing in headwater streams: taxonomic richness versus function. Freshwater Biology, 47, 401–15.CrossRefGoogle Scholar
Hynes, H. B. N. & Kaushik, N. K. (1969). The relationship between dissolved nutrient salts and protein production in submerged autumnal leaves. Verhandlungen der Internationale Vereinigung für Theoretische und Angewandte Limnologie, 17, 95–103.Google Scholar
Iqbal, S. H. & Webster, J. (1973). Aquatic hyphomycete spora of the River Exe and its tributaries. Transactions of the British Mycological Society, 61, 331–46.CrossRefGoogle Scholar
Kaushik, N. K. & Hynes, H. B. N. (1971). The fate of dead leaves that fall into streams. Archiv für Hydrobiologie, 68, 465–515.Google Scholar
Komínková, D., Kuehn, K. A., Büsing, N., Steiner, D. & Gessner, M. O. (2000). Microbial biomass, growth, and respiration associated with submerged litter of Phragmites australis decomposing in a littoral reed stand of a large lake. Aquatic Microbial Ecology, 22, 271–82.CrossRefGoogle Scholar
Kreeger, D. A. & Newell, R. I. E. (2000). Trophic complexity between producers and invertebrate consumers in salt marshes. In Concepts and Controversies in Tidal Marsh Ecology, ed. Weinstein, P. & Kreeger, D. A.. Dordrecht: Kluwer Academic Publishers, pp. 187–220.CrossRefGoogle Scholar
Kuehn, K. A. & Suberkropp, K. (1998a). Decomposition of standing litter of the freshwater macrophyte Juncus effusus L. Freshwater Biology, 40, 717–27.CrossRefGoogle Scholar
Kuehn, K. A. & Suberkropp, K. (1998b). Diel fluctuations in microbial activity associated with standing-dead litter of the freshwater emergent macrophyte Juncus effusus. Aquatic Microbial Ecology, 14, 171–82.CrossRefGoogle Scholar
Kuehn, K. A., Churchill, P. F. & Suberkropp, K. (1998). Osmoregulatory strategies of fungal populations inhabiting standing dead litter of the emergent macrophyte Juncus effusus. Applied and Environmental Microbiology, 64, 607–12.Google Scholar
Kuehn, K. A., Gessner, M. O., Wetzel, R. G. & Suberkropp, K. (1999). Standing litter decomposition of the emergent macrophyte Erianthus giganteus. Microbial Ecology, 38, 50–7.CrossRefGoogle ScholarPubMed
Kuehn, K. A., Lemke, M. J., Suberkropp, K. & Wetzel, R. G. (2000). Microbial biomass and production associated with decaying leaf litter of the emergent macrophyte Juncus effusus. Limnology and Oceanography, 45, 862–70.CrossRefGoogle Scholar
Kuehn, K. A., Steiner, D. & Gessner, M. O. (2004). Diel mineralization patterns of standing-dead plant litter: implications for CO2 flux from wetlands. Ecology, 85, 2504–18.CrossRefGoogle Scholar
Larmola, T., Alm, J., Juutinen, S., Martikainen, P. J. & Silvola, J. (2003). Ecosystem CO2 exchange and plant biomass in the littoral zone of a boreal eutrophic lake. Freshwater Biology, 48, 1295–310.CrossRefGoogle Scholar
Laughlin, R. J. & Stevens, R. J. (2002). Evidence for fungal dominance of denitrification and codenitrification in a grassland soil. Soil Science Society of America Journal, 66, 1540–8.CrossRefGoogle Scholar
Mann, K. H. (1988). Production and use of detritus in various freshwater, estuarine and coastal marine ecosystems. Limnology and Oceanography, 33, 910–30.Google Scholar
Melillo, J. M., Aber, J. D. & Muratore, J. F. (1982). Nitrogen and lignin control of hardwood leaf litter decomposition dynamics. Ecology, 63, 621–6.CrossRefGoogle Scholar
Melillo, J. M., Naiman, R. J., Aber, J. D. & Eshleman, K. N. (1983). The influence of substrate quality and stream size on wood decomposition dynamics. Oecologia, 58, 281–5.CrossRefGoogle ScholarPubMed
Melillo, J. M., Naiman, R. J., Aber, J. D. & Linkins, A. E. (1984). Factors controlling mass-loss and nitrogen dynamics of plant litter decaying in northern streams. Bulletin of Marine Science, 35, 341–56.Google Scholar
Methvin, B. R. & Suberkropp, K. (2003). Annual production of leaf-decaying fungi in 2 streams. Journal of the North American Benthological Society, 22, 554–64.CrossRefGoogle Scholar
Mille-Lindblom, C., Wachenfeldt, E. & Tranvik, L. J. (2004). Ergosterol as a measure of living fungal biomass: persistence in environmental samples after fungal death. Journal of Microbiological Methods, 59, 253–62.CrossRefGoogle ScholarPubMed
Mitsch, W. J. & Gosselink, J. G. (2000). Wetlands, 3rd edn. New York: Wiley & Sons.Google Scholar
Molinero, J., Pozo, J. & Gonzalez, E. (1996). Litter breakdown in streams of the Agüera catchment: Influence of dissolved nutrients and land use. Freshwater Biology, 36, 745–56.CrossRefGoogle Scholar
Moran, M. A., Legovic, T., Benner, R. & Hodson, R. E. (1988). Carbon flow from lignocellulose: a simulation analysis of a detritus-based ecosystem. Ecology, 69, 1525–36.CrossRefGoogle Scholar
Moran, M. A., Benner, R. & Hodson, R. E. (1989). Kinetics of microbial degradation of vascular plant material in two wetland ecosystems. Oecologia, 79, 158–67.CrossRefGoogle ScholarPubMed
Mulholland, P. J., Tank, J. L., Sanzone, D. M.et al. (2000). Nitrogen cycling in a forest stream determined by a N-15 tracer addition. Ecological Monographs, 70, 471–93.Google Scholar
Newbold, J. D., Elwood, J. W., O'Neill, R. V. & Winkle, W. (1981). Measuring nutrient spiralling in streams. Canadian Journal of Fisheries and Aquatic Sciences, 38, 860–3.CrossRefGoogle Scholar
Newell, S. Y. (1993). Decomposition of shoots of a saltmarsh grass: methodology and dynamics of microbial assemblages. Advances in Microbial Ecology, 13, 301–26.CrossRefGoogle Scholar
Newell, S. Y. (2003). Fungal content and activities in standing-decaying leaf blades of plants of the Georgia Coastal Ecosystem research area. Aquatic Microbial Ecology, 32, 95–103.CrossRefGoogle Scholar
Newell, S. Y. & Bärlocher, F. (1993). Removal of fungal and total organic matter from decaying cordgrass leaves by shredder snails. Journal of Experimental Marine Biology and Ecology, 171, 39–49.CrossRefGoogle Scholar
Newell, S. Y. & Fallon, R. D. (1991). Toward a method for measuring instantaneous fungal growth rates in field samples. Ecology, 72, 1547–59.CrossRefGoogle Scholar
Newell, S. Y. & Porter, D. (2000). Microbial secondary production from salt marsh-grass shoots, and its known potential fates. In Concepts and Controversies in Tidal Marsh Ecology, ed. Weinstein, M. P. & Kreeger, D. A.. Dordrecht: Kluwer Academic Publishers, pp. 159–86.CrossRefGoogle Scholar
Newell, S. Y. & Statzell-Tallman, A. (1982). Factors for conversion of fungal biovolume values to biomass, carbon and nitrogen: variation with mycelial ages, growth conditions, and strains of fungi from a salt marsh. Oikos, 39, 261–8.CrossRefGoogle Scholar
Newell, S. Y., Moran, M. A., Wicks, R. & Hodson, R. E. (1995). Productivities of microbial decomposers during early stages of decomposition of leaves of a freshwater sedge. Freshwater Biology, 34, 135–48.CrossRefGoogle Scholar
Niyogi, D. K., Simon, K. S. & Townsend, C. R. (2003). Breakdown of tussock grass in streams along a gradient of agricultural development in New Zealand. Freshwater Biology, 48, 1698–708.CrossRefGoogle Scholar
Ostrofsky, M. L. (1997). Relationship between chemical characteristics of autumn-shed leaves and aquatic processing rates. Journal of the North American Benthological Society, 16, 750–9.CrossRefGoogle Scholar
Paul, E. A. & Clark, F. E. (1989). Soil Microbiology and Biochemistry. San Diego: Academic Press.Google Scholar
Qualls, R. G. (1984). The role of leaf litter nitrogen immobilization in the nitrogen budget of a swamp stream. Journal of Environmental Quality, 13, 640–4.CrossRefGoogle Scholar
Quinn, J. M., Burrell, G. P. & Parkyn, S. M. (2000). Influences of leaf toughness and nitrogen content on in-stream processing and nutrient uptake by litter in a Waikato, New Zealand, pasture stream and streamside channels. New Zealand Journal of Marine and Freshwater Research, 34, 253–71.CrossRefGoogle Scholar
Ramírez, A., Pringle, C. M. & Molina, L. (2003). Effects of stream phosphorus levels on microbial respiration. Freshwater Biology, 48, 88–97.CrossRefGoogle Scholar
Rier, S. T., Tuchman, N. C., Wetzel, R. G. & Teeri, J. A. (2002). Elevated-CO2-induced changes in the chemistry of quaking aspen (Populus tremuloides Michaux) leaf litter: subsequent mass loss and microbial response in a stream ecosystem. Journal of the North American Benthological Society, 21, 16–27.CrossRefGoogle Scholar
Roden, E. E. & Wetzel, R. G. (1996). Organic carbon oxidation and suppression of methane production by microbial Fe(III) oxide reduction in vegetated and unvegetated freshwater wetland sediments. Limnology and Oceanography, 41, 1733–48.CrossRefGoogle Scholar
Rodewald-Rudescu, L. (1974). Das Schilfrohr. (Die Binnengewässer, vol. 27). Stuttgart: Schweizerbart.
Sanzone, D. M., Tank, J. L., Meyer, J. L., Mulholland, P. J. & Findlay, S. E. G. (2001). Microbial incorporation of nitrogen in stream detritus. Hydrobiologia, 464, 27–35.CrossRefGoogle Scholar
Scanlon, D. & Moore, T. (2000). Carbon dioxide production from peatland soil profiles: the influence of temperature, oxic/anoxic conditions and substrate. Soil Science, 165, 153–60.CrossRefGoogle Scholar
Shearer, C. A. (1992). The role of woody debris. In The Ecology of Aquatic Hyphomycetes, ed. Bärlocher, F.. Berlin: Springer-Verlag, pp. 77–98.CrossRefGoogle Scholar
Shoun, H., Kim, D. H., Uchiyama, H. & Sugiyama, J. (1992). Denitrification by fungi. FEMS Microbiology Letters, 94, 277–81.CrossRefGoogle Scholar
Silliman, B. R. & Newell, S. Y. (2003). Fungal farming in a snail. Proceedings of the National Academy of Sciences of the United States of America, 100, 15643–8.CrossRefGoogle Scholar
Simon, K. S. & Benfield, E. F. (2001). Leaf and wood breakdown in cave streams. Journal of the North American Benthological Society, 20, 550–63.CrossRefGoogle Scholar
Sinsabaugh, R. L. & Findlay, S. (1995). Microbial production, enzyme activity, and carbon turnover in surface sediments of the Hudson River estuary. Microbial Ecology, 30, 127–41.CrossRefGoogle ScholarPubMed
Sinsabaugh, R. L., Antibus, R. K., Linkins, A. E.et al. (1993). Wood decomposition: nitrogen and phosphorus dynamics in relation to extracellular enzyme activity. Ecology, 74, 1586–93.CrossRefGoogle Scholar
Sridhar, K. R. & Bärlocher, F. (2000). Initial colonization, nutrient supply, and fungal activity on leaves decaying in streams. Applied and Environmental Microbiology, 66, 1114–19.CrossRefGoogle ScholarPubMed
Stelzer, R. S., Heffernan, J. & Likens, G. E. (2003). The influence of dissolved nutrients and particulate organic matter quality on microbial respiration and biomass in a forest stream. Freshwater Biology, 48, 1925–37.CrossRefGoogle Scholar
Suberkropp, K. (1991). Relationships between growth and sporulation of aquatic hyphomycetes on decomposing leaf litter. Mycological Research, 95, 843–50.CrossRefGoogle Scholar
Suberkropp, K. (1992). Interactions with invertebrates. In The Ecology of Aquatic Hyphomycetes, ed. Bärlocher, F.. Berlin: Springer-Verlag, pp. 118–34.Google Scholar
Suberkropp, K. (1995). The influence of nutrients on fungal growth, productivity, and sporulation during leaf breakdown in streams. Canadian Journal of Botany, 73 (Suppl. 1), S1361–9.CrossRefGoogle Scholar
Suberkropp, K. (1997). Annual production of leaf-decaying fungi in a woodland stream. Freshwater Biology, 38, 169–78.CrossRefGoogle Scholar
Suberkropp, K. (1998a). Effect of dissolved nutrients on two aquatic hyphomycetes growing on leaf litter. Mycological Research, 102, 998–1002.CrossRefGoogle Scholar
Suberkropp, K. (1998b). Microorganisms and organic matter processing. In River Ecology and Management: Lessons from the Pacific Coastal Ecoregion, eds. Naiman, R. J., & Bilby, R. E.. New York: Springer-Verlag, pp. 120–43.CrossRefGoogle Scholar
Suberkropp, K. & Chauvet, E. (1995). Regulation of leaf breakdown by fungi in streams: Influences of water chemistry. Ecology, 76, 1433–45.CrossRefGoogle Scholar
Suberkropp, K. & Klug, M. J. (1980). The maceration of deciduous leaf litter by aquatic hyphomycetes. Canadian Journal of Botany, 58, 1025–31.CrossRefGoogle Scholar
Suberkropp, K. & Weyers, H. (1996). Application of fungal and bacterial production methodologies to decomposing leaves in streams. Applied and Environmental Microbiology, 62, 1610–15.Google ScholarPubMed
Suberkropp, K., Godshalk, G. L. & Klug, M. J. (1976). Changes in the chemical composition of leaves during processing in a woodland stream. Ecology, 57, 720–77.CrossRefGoogle Scholar
Suberkropp, K., Arsuffi, T. L. & Anderson, J. P. (1983). Comparison of degradative ability, enzymatic activity, and palatability of aquatic hyphomycetes grown on leaf litter. Applied and Environmental Microbiology, 46, 237–44.Google ScholarPubMed
Tank, J. L. & Dodds, W. K. (2003). Nutrient limitation of epilithic and epixylic biofilms in ten North American streams. Freshwater Biology, 48, 1031–49.CrossRefGoogle Scholar
Tank, J. L., Webster, J. R. & Benfield, E. F. (1993). Microbial respiration on decaying leaves and sticks in a southern Appalachian stream. Journal of the North American Benthological Society, 12, 394–405.CrossRefGoogle Scholar
Tank, J. L., Meyer, J. L., Sanzone, D. M.et al. (2000). Analysis of nitrogen cycling in a forest stream during autumn using a N-15-tracer addition. Limnology and Oceanography, 45, 1013–29.CrossRefGoogle Scholar
Thormann, M. N., Bayley, S. E. & Currah, R. S. (2001). Comparison of decomposition of belowground and aboveground plant litters in peatlands of boreal Alberta, Canada. Canadian Journal of Botany, 79, 9–22.CrossRefGoogle Scholar
Thornton, D. R. (1963). The physiology and nutrition of some aquatic hyphomycetes. Journal of General Microbiology, 33, 23–31.CrossRefGoogle ScholarPubMed
Thornton, D. R. (1965). Amino acid analysis of fresh leaf litter and the nitrogen nutrition of some aquatic hyphomycetes. Canadian Journal of Microbiology, 11, 657–62.CrossRefGoogle ScholarPubMed
Triska, F. J. & Sedell, J. R. (1976). Decomposition of four species of leaf litter in response to nitrate manipulation. Ecology, 57, 783–92.CrossRefGoogle Scholar
Updegraff, K., Bridgham, S. D., Pastor, J., Weishampel, P. & Harth, C. (2001). Response of CO2 and CH4 emissions from peatlands to warming and water table manipulation. Ecological Applications, 11, 311–26.Google Scholar
Wallander, H., Nilsson, L. O., Hagerberg, D. & Rosengren, U. (2003). Direct estimates of C:N ratios of ectomycorrhizal mycelia collected from Norway spruce forest soils. Soil Biology & Biochemistry, 35, 997–9.CrossRefGoogle Scholar
Wallander, H., Goransson, H. & Rosengren, U. (2004). Production, standing biomass and natural abundance of N-15 and C-13 in ectomycorrhizal mycelia collected at different soil depths in two forest types. Oecologia, 139, 89–97.CrossRefGoogle Scholar
Webster, J. (1959). Experiments with spores of aquatic hyphomycetes I. Sedimentation, and impaction on smooth surfaces. Annals of Botany New Series, 23, 595–611.CrossRefGoogle Scholar
Webster, J. R. & Benfield, E. F. (1986). Vascular plant breakdown in freshwater ecosystems. Annual Review of Ecology and Systematics, 17, 567–94.CrossRefGoogle Scholar
Webster, J. & Davey, R. A. (1984). Sigmoid conidial shape in aquatic fungi. Transactions of the British Mycological Society, 83, 43–52.CrossRefGoogle Scholar
Webster, J. R. & Meyer, J. L. (eds.) (1997). Stream organic matter budgets. Journal of the North American Benthological Society, 16, 3–161.CrossRefGoogle Scholar
Welsch, M. & Yavitt, J. B. (2003). Early stages of decay of Lythrum salicaria L. and Typha latifolia L. in a standing-dead position. Aquatic Botany, 75, 45–57.CrossRefGoogle Scholar
Wetzel, R. G. & Howe, M. J. (1999). High production in a herbaceous perennial plant achieved by continuous growth and synchronized population dynamics. Aquatic Botany, 64, 111–29.CrossRefGoogle Scholar
Weyers, H. S. & Suberkropp, K. (1996). Fungal and bacterial production during the breakdown of yellow poplar leaves in two streams. Journal of the North American Benthological Society, 15, 408–20.CrossRefGoogle Scholar
Yavitt, J. B. (1997). Methane and carbon dioxide dynamics in Typha latifolia (L.) wetlands in central New York State. Wetlands, 17, 394–406.CrossRefGoogle Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×