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Advances in the aquatic sciences
RESEARCH ARTICLE

Potential of submerged macrophytes to support food webs in lowland agricultural streams

Robyn L. Paice A B , Jane M. Chambers A and Belinda J. Robson A
+ Author Affiliations
- Author Affiliations

A Environmental and Conservation Sciences, Murdoch University, 90 South Street, Murdoch, WA 6150, Australia.

B Corresponding author. Email: robyn.paice@westnet.com.au

Marine and Freshwater Research 68(3) 549-562 https://doi.org/10.1071/MF15391
Submitted: 19 October 2015  Accepted: 19 March 2016   Published: 3 June 2016

Abstract

Submerged plants are often abundant in lowland streams in agricultural landscapes, but little is known of their role in stream ecosystems compared to riparian vegetation. We investigated the importance of submerged macrophytes as a basal resource of food webs in stream reaches with good and poor riparian vegetation condition, using mixing model analysis with stable carbon and nitrogen isotopes. Epilithic periphyton and terrestrial detritus were important basal resources in good condition reaches, although where macrophytes were present they contributed to food webs. Higher assimilation of either the macrophyte Cycnogeton huegelii or conspicuous epiphytes on C. huegelii leaves was associated with poor riparian condition. Where Potamogeton ochreatus and Ottelia ovalifolia occurred in poor condition reaches, these macrophytes contributed moderately to the food web, but were probably of greater importance as substrates for epiphytic algae. Mixing models indicated invertebrates commonly had generalist feeding strategies, feeding on the most available resource at each reach. Thus, where riparian vegetation is limited, submerged macrophytes may support opportunistic consumers both directly and as a substrate for epiphytes, thereby partially compensating for the loss of allochthonous resources in lowland agricultural streams.

Additional keywords: aquatic plants, Cycnogeton, intermittent streams, Ottelia, Potamogeton, stable isotopes, trophic.


References

ANZECC and ARMCANZ (2000). ‘Australian and New Zealand Guidelines for Fresh and Marine Water Quality.’ National Water Quality Management Strategy. (Department of the Environment, Australian and New Zealand Environment and Conservation Council and Agriculture and Resource Management Council of Australia and New Zealand: Canberra.)

Beatty, S. J. (2006). The diet and trophic positions of translocated, sympatric populations of Cherax destructor and Cherax cainii in the Hutt River, Western Australia: evidence of resource overlap. Marine and Freshwater Research 57, 825–835.
The diet and trophic positions of translocated, sympatric populations of Cherax destructor and Cherax cainii in the Hutt River, Western Australia: evidence of resource overlap.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28Xht1OgsLfP&md5=503053ecd56fcaa210450d3b76835f45CAS |

Becker, A., and Robson, B. J. (2009). Riverine macroinvertebrate assemblages up to eight years after riparian restoration in a semi-rural catchment in Victoria, Australia. Marine and Freshwater Research 60, 1309–1316.
Riverine macroinvertebrate assemblages up to eight years after riparian restoration in a semi-rural catchment in Victoria, Australia.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhsFOrt7fF&md5=d0313466902b208adbe68ee686516da6CAS |

Bell, N., Riis, T., Suren, A. M., and Baattrup-Pedersen, A. (2013). Distribution of invertebrates within beds of two morphologically contrasting stream macrophyte species. Fundamental and Applied Limnology 183, 309–321.
Distribution of invertebrates within beds of two morphologically contrasting stream macrophyte species.Crossref | GoogleScholarGoogle Scholar |

Bergfur, J., Johnson, R. K., Sandin, L., and Goedkoop, W. (2009). Effects of nutrient enrichment on C and N stable isotope ratios of invertebrates, fish and their food resources in boreal streams. Hydrobiologia 628, 67–79.
Effects of nutrient enrichment on C and N stable isotope ratios of invertebrates, fish and their food resources in boreal streams.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXls12gtLY%3D&md5=9c2e953b62c7be2c35ba1073d3604914CAS |

Blanchette, M. L., Davis, A. M., Jardine, T. D., and Pearson, R. G. (2014). Omnivory and opportunism characterize food webs in a large dry-tropics river system. Freshwater Science 33, 142–158.
Omnivory and opportunism characterize food webs in a large dry-tropics river system.Crossref | GoogleScholarGoogle Scholar |

Bornette, G., and Puijalon, S. (2011). Response of aquatic plants to abiotic factors. Reviews in Aquatic Sciences 73, 1–14.
Response of aquatic plants to abiotic factors.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXht1Wms74%3D&md5=c9a8ddf5e92759ea5ddc6d6da7f9cc0dCAS |

Bunn, S. E., and Boon, P. I. (1993). What sources of organic-carbon drive food webs in billabongs – a study based on stable-isotope analysis. Oecologia 96, 85–94.
What sources of organic-carbon drive food webs in billabongs – a study based on stable-isotope analysis.Crossref | GoogleScholarGoogle Scholar |

Bunn, S. E., Davies, P. M., and Mosisch, T. D. (1999). Ecosystem measures of river health and their response to riparian and catchment degradation. Freshwater Biology 41, 333–345.
Ecosystem measures of river health and their response to riparian and catchment degradation.Crossref | GoogleScholarGoogle Scholar |

Bunn, S. E., Davies, P. M., and Winning, M. (2003). Sources of organic carbon supporting the food web of an arid zone floodplain river. Freshwater Biology 48, 619–635.
Sources of organic carbon supporting the food web of an arid zone floodplain river.Crossref | GoogleScholarGoogle Scholar |

Bunn, S. E., Leigh, C., and Jardine, T. D. (2013). Diet-tissue fractionation of δ15N by consumers from streams and rivers. Limnology and Oceanography 58, 765–773.
Diet-tissue fractionation of δ15N by consumers from streams and rivers.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXptlCqtrw%3D&md5=1cb40d8f49d3034983e4b9b769d90e9aCAS |

Canfield, D. E., and Hoyer, M. V. (1988). Influence of nutrient enrichment and light availability on the abundance of aquatic macrophytes in Florida streams. Canadian Journal of Fisheries and Aquatic Sciences 45, 1467–1472.
Influence of nutrient enrichment and light availability on the abundance of aquatic macrophytes in Florida streams.Crossref | GoogleScholarGoogle Scholar |

Carpenter, S. R., and Lodge, D. M. (1986). Effects of submersed macrophytes on ecosystem processes. Aquatic Botany 26, 341–370.
Effects of submersed macrophytes on ecosystem processes.Crossref | GoogleScholarGoogle Scholar |

Cebrian, J., and Duarte, C. M. (1994). The dependence of herbivory on growth-rate in natural plant communities. Functional Ecology 8, 518–525.
The dependence of herbivory on growth-rate in natural plant communities.Crossref | GoogleScholarGoogle Scholar |

Chessman, B. C. (1986). Dietary studies of aquatic insects from 2 Victorian rivers. Australian Journal of Marine and Freshwater Research 37, 129–146.
Dietary studies of aquatic insects from 2 Victorian rivers.Crossref | GoogleScholarGoogle Scholar |

Chessman, B. C., Westhorpe, D. P., Mitrovic, S. M., and Hardwick, L. (2009). Trophic linkages between periphyton and grazing macroinvertebrates in rivers with different levels of catchment development. Hydrobiologia 625, 135–150.
Trophic linkages between periphyton and grazing macroinvertebrates in rivers with different levels of catchment development.Crossref | GoogleScholarGoogle Scholar |

Clapcott, J. E., and Bunn, S. E. (2003). Can C4 plants contribute to aquatic food webs of agricultural streams? Freshwater Biology 48, 1105–1116.
Can C4 plants contribute to aquatic food webs of agricultural streams?Crossref | GoogleScholarGoogle Scholar |

Davies, P. M. (2010). Climate change implications for river restoration in global biodiversity hotspots. Restoration Ecology 18, 261–268.
Climate change implications for river restoration in global biodiversity hotspots.Crossref | GoogleScholarGoogle Scholar |

Davis, J., and Christidis, F. (1997). ‘A Guide to Wetland Invertebrates of Southwestern Australia.’ (Western Australian Museum: Perth.)

Deegan, B. M., and Ganf, G. G. (2008). The loss of aquatic and riparian plant communities: implications for their consumers in a riverine food web. Austral Ecology 33, 672–683.
The loss of aquatic and riparian plant communities: implications for their consumers in a riverine food web.Crossref | GoogleScholarGoogle Scholar |

Delong, M. D., and Thorp, J. H. (2006). Significance of instream autotrophs in trophic dynamics of the Upper Mississippi River. Oecologia 147, 76–85.
Significance of instream autotrophs in trophic dynamics of the Upper Mississippi River.Crossref | GoogleScholarGoogle Scholar | 16170563PubMed |

Department of Water (2010). ‘Vasse Wonnerup Wetlands and Geographe Bay Water Quality Improvement Plan.’ (Department of Water: Perth.)

Elger, A., Barrat-Segretain, M. H., and Amoros, C. (2002). Plant palatability and disturbance level in aquatic habitats: an experimental approach using the snail Lymnaea stagnalis (l.). Freshwater Biology 47, 931–940.
Plant palatability and disturbance level in aquatic habitats: an experimental approach using the snail Lymnaea stagnalis (l.).Crossref | GoogleScholarGoogle Scholar |

England, L. E., and Rosemond, A. D. (2004). Small reductions in forest cover weaken terrestrial-aquatic linkages in headwater streams. Freshwater Biology 49, 721–734.
Small reductions in forest cover weaken terrestrial-aquatic linkages in headwater streams.Crossref | GoogleScholarGoogle Scholar |

Ferreiro, N., Feijoo, C., Giorgi, A., and Leggieri, L. (2011). Effects of macrophyte heterogeneity and food availability on structural parameters of the macroinvertebrate community in a Pampean stream. Hydrobiologia 664, 199–211.
Effects of macrophyte heterogeneity and food availability on structural parameters of the macroinvertebrate community in a Pampean stream.Crossref | GoogleScholarGoogle Scholar |

Finlay, J. C. (2001). Stable-carbon-isotope ratios of river biota: implications for energy flow in lotic food webs. Ecology 82, 1052–1064.

Fry, B. (2013). Minmax solutions for underdetermined isotope mixing problems: reply to Semmens et al. (2013). Marine Ecology Progress Series 490, 291–294.
Minmax solutions for underdetermined isotope mixing problems: reply to Semmens et al. (2013).Crossref | GoogleScholarGoogle Scholar |

Hamilton, S. K., Lewis, W. M., and Sippel, S. J. (1992). Energy-sources for aquatic animals in the Orinoco River floodplain – evidence from stable isotopes. Oecologia 89, 324–330.
Energy-sources for aquatic animals in the Orinoco River floodplain – evidence from stable isotopes.Crossref | GoogleScholarGoogle Scholar |

Heck, K. L. J., and Crowder, L. B. (1991). Habitat structure and predator-prey interactions in vegetated aquatic systems. In ‘Habitat Structure: the Physical Arrangement of Objects in Space’. (Eds S. S. Bell, E. D. McCoy and H. R. Mushinsky.) pp. 87–106. (Chapman and Hall: London.)

Hershkovitz, Y., and Gasith, A. (2013). Resistance, resilience, and community dynamics in mediterranean-climate streams. Hydrobiologia 719, 59–75.
Resistance, resilience, and community dynamics in mediterranean-climate streams.Crossref | GoogleScholarGoogle Scholar |

Jacobsen, D., and Sand-Jensen, K. (1994). Invertebrate herbivory on the submerged macrophyte Potamogeton perfoliatus in a Danish stream. Freshwater Biology 31, 43–52.
Invertebrate herbivory on the submerged macrophyte Potamogeton perfoliatus in a Danish stream.Crossref | GoogleScholarGoogle Scholar |

Jardine, T. D., Hunt, R. J., Faggotter, S. J., Valdez, D., Burford, M. A., and Bunn, S. E. (2013). Carbon from periphyton supports fish biomass in waterholes of a wet-dry tropical river. River Research and Applications 29, 560–573.
Carbon from periphyton supports fish biomass in waterholes of a wet-dry tropical river.Crossref | GoogleScholarGoogle Scholar |

Johnston, K., Robson, B. J., and Fairweather, P. G. (2011). Trophic positions of omnivores are not always flexible: evidence from four species of freshwater crayfish. Austral Ecology 36, 269–279.
Trophic positions of omnivores are not always flexible: evidence from four species of freshwater crayfish.Crossref | GoogleScholarGoogle Scholar |

Kornijow, R., Gulati, R. D., and Ozimek, T. (1995). Food preference of fresh-water invertebrates – comparing fresh and decomposed angiosperm and a filamentous alga. Freshwater Biology 33, 205–212.
Food preference of fresh-water invertebrates – comparing fresh and decomposed angiosperm and a filamentous alga.Crossref | GoogleScholarGoogle Scholar |

Lake, P. S., Bond, N., and Reich, P. (2007). Linking ecological theory with stream restoration. Freshwater Biology 52, 597–615.
Linking ecological theory with stream restoration.Crossref | GoogleScholarGoogle Scholar |

Leigh, C., Burford, M. A., Sheldon, F., and Bunn, S. E. (2010). Dynamic stability in dry season food webs within tropical floodplain rivers. Marine and Freshwater Research 61, 357–368.
Dynamic stability in dry season food webs within tropical floodplain rivers.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXjvFSjs7Y%3D&md5=172c30ed1b394d5c263b011422192f0eCAS |

McCutchan, J. H., and Lewis, W. M. (2002). Relative importance of carbon sources for macroinvertebrates in a rocky mountain stream. Limnology and Oceanography 47, 742–752.
Relative importance of carbon sources for macroinvertebrates in a rocky mountain stream.Crossref | GoogleScholarGoogle Scholar |

McCutchan, J. H., Lewis, W. M., Kendall, C., and McGrath, C. C. (2003). Variation in trophic shift for stable isotope ratios of carbon, nitrogen, and sulfur. Oikos 102, 378–390.
Variation in trophic shift for stable isotope ratios of carbon, nitrogen, and sulfur.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXmsl2qurg%3D&md5=cda564d4e95e5f058bd46e6a7ea718bdCAS |

McHugh, P., McIntosh, A., Howard, S., and Budy, P. (2012). Niche flexibility and trout-galaxiid co-occurrence in a hydrologically diverse riverine landscape. Biological Invasions 14, 2393–2406.
Niche flexibility and trout-galaxiid co-occurrence in a hydrologically diverse riverine landscape.Crossref | GoogleScholarGoogle Scholar |

Moore, J. W., and Semmens, B. X. (2008). Incorporating uncertainty and prior information into stable isotope mixing models. Ecology Letters 11, 470–480.
Incorporating uncertainty and prior information into stable isotope mixing models.Crossref | GoogleScholarGoogle Scholar | 18294213PubMed |

O’Leary, M. H. (1981). Carbon isotope fractionation in plants. Phytochemistry 20, 553–567.
Carbon isotope fractionation in plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3MXltFWlsLY%3D&md5=adaebb80244066470371b27db91c109dCAS |

Paice, R. L., Chambers, J. M., and Robson, B. J. (2016). Native submerged macrophyte distribution in seasonally flowing, south-western Australian streams in relation to stream condition. Aquatic Sciences , .
Native submerged macrophyte distribution in seasonally flowing, south-western Australian streams in relation to stream condition.Crossref | GoogleScholarGoogle Scholar |

Palmer, M. A., Hondula, K. L., and Koch, B. J. (2014). Ecological restoration of streams and rivers: shifting strategies and shifting goals. Annual Review of Ecology Evolution and Systematics 45, 247–269.
Ecological restoration of streams and rivers: shifting strategies and shifting goals.Crossref | GoogleScholarGoogle Scholar |

Peterson, B. J., and Fry, B. (1987). Stable isotopes in ecosystem studies. Annual Review of Ecology and Systematics 18, 293–320.
Stable isotopes in ecosystem studies.Crossref | GoogleScholarGoogle Scholar |

Phillips, D. L., and Gregg, J. W. (2003). Source partitioning using stable isotopes: coping with too many sources. Oecologia 136, 261–269.
Source partitioning using stable isotopes: coping with too many sources.Crossref | GoogleScholarGoogle Scholar | 12759813PubMed |

Phillips, D. L., and Koch, P. L. (2002). Incorporating concentration dependence in stable isotope mixing models. Oecologia 130, 114–125.
Incorporating concentration dependence in stable isotope mixing models.Crossref | GoogleScholarGoogle Scholar |

Phillips, D. L., Newsome, S. D., and Gregg, J. W. (2005). Combining sources in stable isotope mixing models: alternative methods. Oecologia 144, 520–527.
Combining sources in stable isotope mixing models: alternative methods.Crossref | GoogleScholarGoogle Scholar | 15711995PubMed |

Phillips, D. L., Inger, R., Bearhop, S., Jackson, A. L., Moore, J. W., Parnell, A. C., Semmens, B. X., and Ward, E. J. (2014). Best practices for use of stable isotope mixing models in food-web studies. Canadian Journal of Zoology 92, 823–835.
Best practices for use of stable isotope mixing models in food-web studies.Crossref | GoogleScholarGoogle Scholar |

Post, D. M., Layman, C. A., Arrington, D. A., Takimoto, G., Quattrochi, J., and Montana, C. G. (2007). Getting to the fat of the matter: models, methods and assumptions for dealing with lipids in stable isotope analyses. Oecologia 152, 179–189.
Getting to the fat of the matter: models, methods and assumptions for dealing with lipids in stable isotope analyses.Crossref | GoogleScholarGoogle Scholar | 17225157PubMed |

Power, M. E., Holomuzki, J. R., and Lowe, R. L. (2013). Food webs in Mediterranean rivers. Hydrobiologia 719, 119–136.
Food webs in Mediterranean rivers.Crossref | GoogleScholarGoogle Scholar |

Reid, D. J., Lake, P. S., Quinn, G. P., and Reich, P. (2008a). Association of reduced riparian vegetation cover in agricultural landscapes with coarse detritus dynamics in lowland streams. Marine and Freshwater Research 59, 998–1014.
Association of reduced riparian vegetation cover in agricultural landscapes with coarse detritus dynamics in lowland streams.Crossref | GoogleScholarGoogle Scholar |

Reid, D. J., Quinn, G. P., Lake, P. S., and Reich, P. (2008b). Terrestrial detritus supports the food webs in lowland intermittent streams of south-eastern Australia: a stable isotope study. Freshwater Biology 53, 2036–2050.
Terrestrial detritus supports the food webs in lowland intermittent streams of south-eastern Australia: a stable isotope study.Crossref | GoogleScholarGoogle Scholar |

Skrzypek, G., and Paul, D. (2006). δ13C analysis of calcium carbonate: comparison between the gasbench and elemental analyzer techniques. Rapid Communications in Mass Spectrometry 20, 2915–2920.
δ13C analysis of calcium carbonate: comparison between the gasbench and elemental analyzer techniques.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhtVylsr%2FJ&md5=a1667bdd062cda57ded1a0733613fde3CAS | 16941549PubMed |

Skrzypek, G., Sadler, R., and Debajyoti, P. (2010). Error propagation in normalization of stable isotope data: a Monte Carlo analysis. Rapid Communications in Mass Spectrometry 24, 2697–2705.
Error propagation in normalization of stable isotope data: a Monte Carlo analysis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtFWhu73E&md5=8143c7ff723820584953eff88e094c2dCAS | 20814975PubMed |

St Clair, R. M. (1994). Diets of some larval Leptoceridae (Trichoptera) in south-eastern Australia. Australian Journal of Marine and Freshwater Research 45, 1023–1032.
Diets of some larval Leptoceridae (Trichoptera) in south-eastern Australia.Crossref | GoogleScholarGoogle Scholar |

Stock, B. C., and Semmens, B. X. (2013). Mixsiar GUI user manual, version 1.0. Available at https://github.com/brianstock/MixSIAR [Verified 10 September 2014].

Strayer, D. L., and Malcom, H. M. (2007). Submersed vegetation as habitat for invertebrates in the Hudson River estuary. Estuaries and Coasts 30, 253–264.
Submersed vegetation as habitat for invertebrates in the Hudson River estuary.Crossref | GoogleScholarGoogle Scholar |

Thorp, J. H., Delong, M. D., Greenwood, K. S., and Casper, A. F. (1998). Isotopic analysis of three food web theories in constricted and floodplain regions of a large river. Oecologia 117, 551–563.
Isotopic analysis of three food web theories in constricted and floodplain regions of a large river.Crossref | GoogleScholarGoogle Scholar |

Udy, J. W., and Bunn, S. E. (2001). Elevated δ15N values in aquatic plants from cleared catchments: why? Marine and Freshwater Research 52, 347–351.
Elevated δ15N values in aquatic plants from cleared catchments: why?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXlt1Gmu7s%3D&md5=f4ed8106052132e9fd45cac5e3d13a66CAS |

Vanderklift, M. A., and Ponsard, S. (2003). Sources of variation in consumer-diet δ15N enrichment: a meta-analysis. Oecologia 136, 169–182.
Sources of variation in consumer-diet δ15N enrichment: a meta-analysis.Crossref | GoogleScholarGoogle Scholar | 12802678PubMed |

Vannote, R. L., Minshall, G. W., Cummins, K. W., Sedell, J. R., and Cushing, C. E. (1980). River continuum concept. Canadian Journal of Fisheries and Aquatic Sciences 37, 130–137.
River continuum concept.Crossref | GoogleScholarGoogle Scholar |

Warfe, D. M., and Barmuta, L. A. (2006). Habitat structural complexity mediates food web dynamics in a freshwater macrophyte community. Oecologia 150, 141–154.
Habitat structural complexity mediates food web dynamics in a freshwater macrophyte community.Crossref | GoogleScholarGoogle Scholar | 16932971PubMed |

Water and Rivers Commission (1999). Planning and management: foreshore condition assessment in farming areas of south-west Western Australia. River Restoration Report RR3. (Water and Rivers Commission: Perth, WA, Australia.) Available at http://www.water.wa.gov.au/water-topics/waterways/assessing-waterway-health/foreshore-condition-and-assessment [Verified 4 May 2016].

Watson, A., and Barmuta, L. A. (2011). Feeding-preference trials confirm unexpected stable isotope analysis results: freshwater macroinvertebrates do consume macrophytes. Marine and Freshwater Research 62, 1248–1257.
Feeding-preference trials confirm unexpected stable isotope analysis results: freshwater macroinvertebrates do consume macrophytes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhtlagu7nK&md5=50ee7862a091d4cf6edf87fd9a76be4fCAS |