Ecology: Elodea canadensis is a perennial aquatic herb introduced to several river systems across all continents except South America and Antarctica (Kubrak et al. 2012). In North America, E. canadensis is commonly observed in nutrient-rich, neutral to slightly alkaline waters (Spicer and Catling 1988; Holm et al. 1997). The species is typically rooted in mud (Bowmer et al. 1995). It prefers cooler conditions, with an optimum water temperature of 10-25 °C, but has the ability to survive and slowly grow under ice cover (Cook and Urmi-Konig 1985; Bowmer et al. 1995). It is only found in cold water in Australia and has been observed in shallow lakes and streams across Europe and North America (Bowmer et al. 1995; Ersoy and Turan 2019; Josefsson and Andersson 2002). As the plant dies during the fall, it turns black and releases ions, particularly manganese, into the water (Cook and Urmi-Konig 1985). Seed formation is rare for E. canadensis, instead, the species reproduces vegetatively through dispersal of stem pieces moved by water and waterfowl resulting in rapid growth, especially in soils rich in iron (Spicer and Catling 1988; Cook and Urmi-Konig, 1985; Josefsson and Andersson 2002). Growth in the species occurs immediately after the temperature starts rising and light intensity increases in the spring (Cook and Urmi-Konig 1985; Nichols and Shaw 1986). Its water content can range between 85-95% (Holm et al. 1997). It tends to optimally grow in 3-4 m water depth (Mjelde et al. 2012). In its native range, dense beds of E. canadensis tend to decrease the efficiency of irrigated agriculture (Spicer and Catling 1988). Elodea canadensis provides both cover and food for aquatic invertebrates, in turn, increasing the number of invertebrates and the overall food availability for ducks and fish (Spicer and Catling 1988).
Impact of Introduction: Summary of species impacts derived from literature review. Click on an icon to find out more...
Elodea canadensis has been observed altering habitats and changing community structure. In Norway, the spread of E. canadensis resulted in a Najas flexilis (nodding waternymph) dominated community to become fully dominated by E. canadensis in a 25 year period (Mjelde et al. 2012). Additionally, in Steinsfjord, Norway, the vast spread of E. canadensis displaced every macrophyte across all sediment types (Rørslett et al. 1986). In Poland, the extensive spread of E. canadensis poses a potential threat to various valuable elements of Polish aquatic flora, occupying vegetative land in 40% of the analyzed lakes (Kolada and Kutyla 2016). In three different Swedish lakes, E. canadensis significantly outgrew all native species except Fontinalis antipyretica (Tattersdill et al. 2017).
It is speculated that the first record of E. canadensis in Sapanca Lake in Turkey is a contributing factor in the overall alteration of biodiversity dynamics within the lake (Ersoy and Turan 2019). In Kilpiaistenpohja Bay, Finland, it was found that as the density of E. canadensis increased, the total biomass of the crustacean Daphnia longispina decreased (Kornijów et al. 2004). A study, conducted by the University of Lyon, France found that dense stands of E. canadensis can reduce light penetration, ultimately creating anoxic conditions in the water (Barrat-Segretain, 2005; Tattersdill et al. 2017).
In Lake Mälaren, Sweden, dense stands of E. canadensis become coated with calcium carbonate, which precipitates in lime-rich waters during photosynthesis periods, raising overall pH (Josefsson and Andersson 2001). Additionally in Central Sweden, low light conditions in water resulting from the cover of dense E. canadensis stands increased phosphate and total organic carbon concentrations (Tattersdill et al. 2017). Elodea canadensis populations in Steinsfjord, Norway stored significant amounts of carbon, nitrogen, potassium, and phosphorous throughout the summer, with nitrogen increasing near the lake floor due to the presence of substantial amounts of ammonium taken from organic decomposition (Rørslett et al. 1986).
Dense stands of E. canadensis obstructed the use of boat ramps in Lake Taupo, New Zealand (Bowmer et. al. 1995). Their dense beds have similarly restricted water traffic and obstructed water-based recreation in Ontario, tBritish Columbia, Southern Quebec, and Alberta (Spicer and Catling 1988).
In addition, E. canadensis has impacted the infrastructure, agriculture, and predation patterns of the environments it’s invaded. Throughout New Zealand, E. canadensis has partially clogged screen intakes in various hydropower stationHoward-Williams 1993).
References: (click for full references)
Barrat-Segretain, M.H. 2005. Competition between invasive and indigenous species: impact of spatial pattern and developmental stage. Plant Ecology 180(2):153-160. https://www.jstor.org/stable/20146803.
Bowmer, K. H., S. W. L. Jacobs, and G. R. Sainty. 1995. Identification, biology, and management of Elodea canadensis, Hydrocharitaceae. Journal of Aquatic Plant Management, 33, 13-19.
Cook, C.D. and K. Urmi-König. 1985. A revision of the genus Elodea (Hydrocharitaceae). Aquatic Botany, 21(2), pp.111-156.
Ersoy, S., and Y.A. Turan. 2019. First report on the cocurrence of invasive macrophyte Elodea canadensis Michx. in Sapanca Lake. European Journal of Biology 78(2):103-107. https://doi.org/10.26650/EurJBiol.2019.0018.
Holm, L., J. Doll, E. Holm, J. Pancho, and J. Herberger. 1997. World Weeds: natural histories and distribution, New York, USA: John Wiley and Sons. Available: https://books.google.la/books?id=i7JjRXH6uq4C&printsec=copyright#v=onepage&q=canadensis&f=false
Howard-Williams, C. 1993. Processes of aquatic weed invasions: the New Zealand example. Journal of Aquatic Plant Management 31:17-23.
Josefsson, M. and B. Andersson. 2001. The environmental consequences of alien species in the Swedish lakes Mälaren, Hjälmaren, Vänern and Vättern. , 30(8), pp.514-521. Ambio: a Journal of the Human Environment 30(8):514-521. https://doi.org/10.1579/0044-7447-30.8.51.
Kolada, A. and S. Kutyla. 2016, Elodea canadensis (Michx.) in Polish lakes: a non-aggressive addition to native flora. Biological Invasions (18) 11: 3251-3264.
Kornijow, R., K. Vakkilainen, J. Horppila, E. Luokkanen, and T. Kairesalo. 2005. Impacts of a submerged plant (Elodea canadensis) on interactions between roach (Rutilus rutilus) and its invertebrate prey communities in a lake littoral zone. Freshwater Biology 50(2):262-276. https://doi.org/10.1111/j.1365-2427.2004.01318.x.
Kubrak, E., J. Kubrak, and P. M. Rowinski. 2013. Application of one-dimensional model to calculate water velocity distributions over elastic elements simulating Canadian waterweed plants (Elodea Canadensis). Acta Geophysica, 61(1), pp.194-210.
Mjelde, M., P. Lombardo, D. Berge, and S. W. Johansen. 2012. Mass invasion of non-native Elodea canadensis Michx. in a large, clear-water, species-rich Norwegian lake–impact on macrophyte biodiversity. In Annales de Limnologie-International Journal of Limnology (Vol. 48, No. 2, pp. 225-240). EDP Sciences.
Nichols S.A., and B. H. Shaw. 1986. Ecological life histories of the three aquatic nuisance plants, Myriophyllum spicatum, Potamogeton crispus and Elodea canadensis. Hydrobiologia, 131, 3–21.
Rørslett, B., D.A.G. Berge, and S.W. Johansen. 1986. Lake enrichment by submersed macrophytes: a Norwegian whole-lake experience with Elodea canadensis. Aquatic Botany 26:325-340.
Simpson D. A. 1986. Taxonomy of Elodea Michx in the British Isles. Watsonia, 16, 1-14.
Spicer, K. W., and P.M. Catling. 1988. The biology of Canadian weeds. 88. Elodea canadensis Michx. Canadian Journal of Plant Science 68:1035-1051.
St. John, H. 1965. Monograph of the genus Elodea, Summary. Rhodora 67(770):155-180.
Tattersdill, K., F. Ecke, A. Frainer, and B.G. McKie. 2017. A head start for an invasive species in a strongly seasonal environment? Growth of Elodea canadensis in boreal lakes. Aquatic Invasions 12(4):487-498. https://doi.org/doi.org/10.3391/ai.2017.12.4.06.
Wells, R. D., M. D. de Winton, and J. S. Clayton. 1997. Successive macrophyte invasions within the submerged flora of Lake Tarawera, central North Island, New Zealand. New Zealand Journal of Marine and Freshwater Research, 31(4), pp.449-459.
This information is preliminary or provisional and is subject to revision. It is being provided to meet the need for timely best science. The information has not received final approval by the U.S. Geological Survey (USGS) and is provided on the condition that neither the USGS nor the U.S. Government shall be held liable for any damages resulting from the authorized or unauthorized use of the information.