Alonso A, Castro-Díez P (2008) What explains the invading success of the aquatic mud snail Potamopyrgus antipodarum (Hydrobiidae, Mollusca)? Hydrobiologia 614:107–116
Google Scholar
Benke AC (1979) A modification to the Hynes method for estimating secondary production with particular significance for multivoltine populations. Limnol Oceanogr 24:168–174
Google Scholar
Benke AC, Huryn AD (2017) Secondary production and quantitative food webs. In: Lamberti GA, Hauer FR (eds) Methods in stream ecology (Third Edition). Academic Press, San Diego, pp 235–254
Google Scholar
Benke AC, Huryn AD, Smock LA, Wallace JB (1999) Length-mass relationships for freshwater macroinvertebrates in North America with particular reference to the southeastern United States. J N Am Benthol Soc 18:308–343
Google Scholar
Benson AJ, Kipp RM, Larson J, Fusaro A (2020) Potamopyrgus antipodarum (J.E. Gray, 1853): U.S. Geological Survey, Nonindigenous Aquatic Species Database, Gainesville, FL, https://nas.er.usgs.gov/queries/factsheet.aspx?SpeciesID=1008, Revision Date: 1/6/2020, Access Date: 10/27/2020.
Bruce RL, Moffitt CM, Dennis B (2009) Survival and passage of ingested New Zealand Mudsnails through the intestinal tract of Rainbow Trout. N Am J Aquacult 71:287–301
Google Scholar
Bunn SE, Arthington AH (2002) Basic principles and ecological consequences of altered flow regimes for aquatic biodiversity. Environ Manage 30:492–507
PubMed
Google Scholar
Butkus R, Višinskienė G (2020) The aquatic invader Potamopyrgus antipodarum (Gray, 1843) is a poorer food item for benthivorous fishes than native snails. Aquat Invasions 15:473–481
Google Scholar
Caton LW (1991) Improved subsampling methods for the EPA rapid bioassessment benthic protocols. Bull N Am Benthol Soc 8:317–319
Google Scholar
Collado GA (2014) Out of New Zealand: molecular identification of the highly invasive freshwater mollusk Potamopyrgus antipodarum (Gray, 1843) in South America. Zool Stud 53:70
Google Scholar
Collier KJ, Wilcock RJ, Meredith AS (1998) Influence of substrate type and physico-chemical conditions on macroinvertebrate faunas and biotic indices of some lowland, Waikato, New Zealand streams. New Zeal J Mar Fresh 32:1–19
Google Scholar
Crooks JA (2002) Characterizing ecosystem-level consequences of biological invasions: the role of ecosystem engineers. Oikos 97:153–166
Google Scholar
Cross WF, Rosi-Marshall EJ, Behn KE, Kennedy TA, Hall RO Jr, Fuller AE, Baxter CV (2010) Invasion and production of New Zealand mud snails in the Colorado River, Glen Canyon. Biol Invasions 12:3033–3043
Google Scholar
Dorgelo J (1987) Density fluctuations in populations (1982–1986) and biological observations of Potamopyrgus jenkinsi in two trophically differing lakes. Hydrol Bull 21:95–110
Google Scholar
Dybdahl MF, Kane SL (2005) Adaptation vs. phenotypic plasticity in the success of a colonial invader. Ecology 86:1592–1601
Google Scholar
Filbert RB, Hawkins CP (1995) Variation in condition of rainbow trout in relation to food, temperature, and individual length in the Green River, Utah. T Am Fish Soc 124:824–835
Google Scholar
Gallardo B, Clavero M, Sánchez MI, Vilá M (2016) Global ecological impacts of invasive species in aquatic ecosystems. Glob Chang Biol 22:151–163
PubMed
Google Scholar
Greenwood DJ, Hall RO Jr, Tibbets TM, Krist AC (2020) A precipitous decline in an invasive snail population cannot be explained by a native predator. Biol Invasions 22:363–378
Google Scholar
Gust M, Buronfosse T, André C, Mons R, Gagné F, Garric J (2011) Is exposure temperature a confounding factor for the assessment of reproductive parameters of New Zealand mudsnails Potamopyrgus antipodarum (Gray)? Aquat Toxicol 101:396–404
PubMed
CAS
Google Scholar
Hall RO Jr, Tank JL, Dybdahl MF (2003) Exotic snails dominate nitrogen and carbon cycling in a highly productive stream. Front Ecol Environ 1:407–411
Google Scholar
Hall RO Jr, Dybdahl MF, VanderLoop MC (2006) Extremely high secondary production of introduced snails in rivers. Ecol Appl 16:1121–1131
PubMed
Google Scholar
Holomuzki JR, Biggs BJF (1999) Distributional response to flow disturbance by a stream-dwelling snail. Oikos 87:36–47
Google Scholar
Holomuzki JR, Biggs BJF (2000) Taxon-specific responses to high-flow disturbances in streams: implications for population persistence. J N Am Benthol Soc 19:670–679
Google Scholar
Holomuzki JR, Biggs BJF (2007) Physical microhabitat effects on 3-dimensioinal spatial variability of the hydrobiid snail, Potamopyrgus antipodarum. New Zeal J Mar Fresh 41:357–367
Google Scholar
Huryn AD (1996) An appraisal of the Allen paradox in a New Zealand trout stream. Limnol Oceanogr 41:243–252
Google Scholar
Kerans BL, Dybdhal MF, Gangloff MM, Jannot JE (2005) Potamopyrgus antipodarum distribution, abundance, and effects on native macroinvertebrates in the greater yellowstone ecosystem. J N Am Benthol Soc 24:123–138
Google Scholar
Kolar CS, Lodge DM (2001) Progress in invasion biology: predicting invaders. Trends Ecol Evol 16:199–204
PubMed
Google Scholar
Loo SE, Mac Nally R, Lake PS (2007) Forecasting New Zealand Mudsnail invasion range: model comparisons using native and invaded ranges. Ecol Appl 17:181–189
PubMed
Google Scholar
McCarter NH (1986) Food and energy in the diet of brown and rainbow trout from Lake Benmore, New Zealand. New Zeal J Mar Fresh 11:357–373
Google Scholar
McKenzie VJ, Hall WE, Guralnick RP (2013) New Zealand mudsnails (Potamopyrgus antipodarum) in Boulder Creek, Colorado: environmental factors associated with fecundity of a parthenogenic invader. Can J Zool 91:30–36
CAS
Google Scholar
Moore JW, Herbst DB, Heady WN, Carlson SM (2012) Stream community and ecosystem responses to the boom and bust of an invading snail. Biol Invasions 14:2435–2446
Google Scholar
R Core Team (2021) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. http://www.R-project.org/
Ribi G (1986) Within-lake dispersal of the prosobranch snails, Viviparus ater and Potamopyrgus jenkinsi. Oecologia 69:60–63
PubMed
Google Scholar
Riley LA, Dybdahl MF, Hall RO Jr (2008) Invasive species impact: asymmetric interactions between invasive and endemic freshwater snails. J North Am Benthol Soc 27:509–520
Google Scholar
Ruhi A, Catford JA, Cross WF, Escoriza D, Olden JD (2019) Understanding the nexus between hydrological alteration and biological invasions. In: Sabater S, Elosegi A, Ludwig R (eds) Multiple stressors in river ecosystems. Elsevier, Cambridge, pp 45–64
Google Scholar
Schisler GJ, Vieira NKM, Walker PG (2008) Application of household disinfectants to control New Zealand Mudsnails. N Am J Fish Manage 28:1172–1176
Google Scholar
Schreiber ESG, Quinn GP, Lake PS (2003) Distribution of an alien aquatic snail in relation to flow variability, human activities, and water quality. Freshw Biol 48:951–961
Google Scholar
Simberloff D, Gibbons L (2004) Now you see them, now you don’t! – population crashed of established introduced species. Biol Invasions 6:161–172
Google Scholar
Strayer DL, D’Antonio CM, Essl F, Fowler MS, Geist J, Hilt S, Jöhnk IJK, Jones CG, Lambin X, Latzka AW, Pergl J, Pyšek RP, von Schmalensee M, Stefansson RA, Wright J, Jeschke JM (2017) Boom-bust dynamics in biological invasions: towards an improved application of the concept. Ecol Lett 20:1337–1350
PubMed
Google Scholar
Towers DJ, Henderson IM, Veltman CJ (1994) Predicting dry weight of New Zealand aquatic macroinvertebrates from linear dimensions. New Zeal J Mar Fresh 28:159–166
Google Scholar
Vinson MR (2001) Long-term dynamics of an invertebrate assemblage downstream from a large dam. Ecol Appl 11:711–730
Google Scholar
Vinson MR, Baker MA (2008) Poor growth of rainbow trout fed New Zealand mud snails, Potamopyrgus antipodarum. N Am J Fish Manage 28:701–709
Google Scholar
Ward JV, Stanford JA (1983) The serial discontinuity concept of lotic ecosystems. In: Fontaine TD, Bartell SM (eds) Dynamics of lotic ecosystems. Ann Arbor Scientific Publishers, Ann Arbor, pp 29–42
Google Scholar
Winterbourn M (1970) The New Zealand species of Potamopyrgus (Gastropoda: Hydrobiidae). Malacologia 10:283–321
Google Scholar