https://doi.org/10.4081/jlimnol.2023.2092
Periphyton growth on allochthonous input in streams may lead to higher individual growth rates of the invasive New Zealand mud snail (Potamopyrgus antipodarum)
Submitted: 9 August 2022
Accepted: 25 May 2023
Published: 20 June 2023
Accepted: 25 May 2023
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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
The aquatic, invasive New Zealand mud snail (Potamopyrgus antipodarum) exploits a variety of food sources. Here we examine the change in growth of snails that fed on periphyton colonizing leaf litter, wood, rock, and a control. Juveniles were grown in the lab on Spirulina algae powder (control) or periphyton grown on rock, leaf litter, or wood. Length was measured at the beginning of the experiment and after eight weeks. Snails grown on leaf litter increased in length more than twice as much as the control and the snails in the rock treatment, and the snails grown on wood showed an increase in length more than twice as much as snails in the rock treatment. This suggests that allochthonous material may contribute to a more nutritious food source for New Zealand mud snails and possibly aid in their invasion success.
Alonso Á, Castro-Díez P, 2008. What explains the invading success of the aquatic mud snail Potamopyrgus antipodarum (Hydrobiidae, Mollusca)? Hydrobiologia 614:107-116.
DOI: https://doi.org/10.1007/s10750-008-9529-3
Alonso Á, Castro-Díez P, 2012. The exotic aquatic mud snail Potamopyrgus antipodarum (Hydrobiidae, Mollusca): state of the art of a worldwide invasion. Aquat. Sci. 74:375-383.
DOI: https://doi.org/10.1007/s00027-012-0254-7
Alonso Á, Collado GA, Gerard C, Levri EP, Salvador RB, Castro-Díez P, 2023. Effects of the invasive aquatic snail Potamopyrgus antipodarum (Gray, 1853) on ecosystem properties and services. Hydrobiologia. Online Ahead of Print.
DOI: https://doi.org/10.1007/s10750-022-05116-z
Arango CP, Riley LA, Tank JL, Hall RO, 2009. Herbivory by an invasive snail increases nitrogen fixation in a nitrogen-limited stream. Can. J. Fish. Aquat. Sci. 66:1309-1317.
DOI: https://doi.org/10.1139/F09-079
Bilka RH, Levri EP, 2013 The invasive New Zealand mud snail (Potamopyrus antipodarum) grows faster when consuming periphyton compared to detritus. J. Pennsylvania Acad. Sci. 87:125-128.
DOI: https://doi.org/10.5325/jpennacadscie.87.3.0125
Bovee EN, Tiegs SD, 2023. Interactions between invasive New Zealand mudsnails and leaf litter: growth and decomposition. Aquat. Ecol. 57:523-528.
DOI: https://doi.org/10.1007/s10452-023-10026-w
Courant J, Vogt S, Marques R, Measey J, Secondi J, Rebelo R, et al., 2017. Are invasive popoulations characterized by a broader diet than native populations? PeerJ 5:e3250.
DOI: https://doi.org/10.7717/peerj.3250
Dorgelo J, 1991. Growth, food and respiration in the prosobranch snail Potamopyrgus jenkinsi in two trophically differing lakes. Hydrobiol. Bull. 21:95-110.
DOI: https://doi.org/10.1007/BF02255459
Dorgelo J, Leonards PE, 2001. Relationship between C/N ratio of food types and growth rate in the snail Potamopyrgus jenkinsi (E. A. Smith). J. N. Am. Benthol. Soc. 20:60-67.
DOI: https://doi.org/10.2307/1468188
Dybdahl MF, Kane SL, 2005. Adaptation vs phenotypic plasticity in the success of a clonal invader. Ecology 86:1592-1601.
DOI: https://doi.org/10.1890/04-0898
Geist JA, Mancuso JL, Morin MM, Bommarito KP, Bovee EN, Wendell D, et al., 2022. The New Zealand mud snail (Potamopyrgus antipodarum): autecology and management of a global invader. Biol. Invasions 24:905-938.
DOI: https://doi.org/10.1007/s10530-021-02681-7
Hall RO, Dybdahl MF, Vanderloop MC, 2006. Extremely high secondary production of introduced snails in rivers. Ecol. Appl. 16:1121-1131.
DOI: https://doi.org/10.1890/1051-0761(2006)016[1121:EHSPOI]2.0.CO;2
Hansen BK, Krist AC, Tibbets TM. 2016. Foraging differences between the native snail, Fossaria sp. and the invasive New Zealand mud snail (Potamopyrgus antipodarum) in response to phosphorus limitation. Aquat. Ecol. 50:297-306.
DOI: https://doi.org/10.1007/s10452-016-9578-z
Krist AC, Charles CC. 2012. The invasive New Zealand mud snail, Potamopyrgus antipodarum, is an effective grazer of algae and altered the assemblage of diatoms more than native grazers. Hydrobiologia 694:143-151.
DOI: https://doi.org/10.1007/s10750-012-1138-5
Levri EP, Berkheimer C, Wilson K, Xu J, Woods T, Hutchinson S, et al., 2020. The cost of predator avoidance behaviors in an invasive freshwater snail. Freshw. Sci. 39:476-484.
DOI: https://doi.org/10.1086/710107
Levri EP, Clark TJ, 2015. Behavior in invasive New Zealand mud snails (Potamopyrgus antipodarum) is related to source population. Biol. Invasions 17:497-506.
DOI: https://doi.org/10.1007/s10530-014-0746-6
Levri EP, Landis S, Smith BJ, 2017a. A periphyton-based diet results in an increased growth rate compared to a detritus-based diet in the invasive New Zealand mud snail (Potamopyrgus antipodarum). Am. Malacol. Bull. 35:65-69.
DOI: https://doi.org/10.4003/006.035.0109
Levri EP, Landis S, Smith BJ, College E, Metz E, Li X, 2017b. Variation in predator-induced behavioral changes in introduced and native populations of the invasive New Zealand mud snail Potamopyrgus antipodarum (Gray, 1843). Aquat. Invasions 12:499-508.
DOI: https://doi.org/10.3391/ai.2017.12.4.07
Liess A, Lange K, 2011. The snail Potamopyrgus antipodarum grows faster and is more active in the shade, independent of food quality. Oecologia 167:85-96.
DOI: https://doi.org/10.1007/s00442-011-1963-7
Proctor T, Kerans B, Clancey P, Ryce E, Dybdahl M, Gustafson D, et al., 2007. National management and control plan for the New Zealand mudsnail (Potamopyrgus antipodarum). Available from: https://www.landcan.org/pdfs/NZMS_MgmtControl_Final.pdf
Riley LA, Dybdahl MF. 2015. The roles of resource availability and competition in mediating growth rates of invasive and native freshwater snails. Freshwater Biology 60:1308-1315.
DOI: https://doi.org/10.1111/fwb.12566
Riley LA, Dybdahl MF, Hall RO. 2008. Invasive species impact: asymmetric interactions between invasive and endemic freshwater snails. J. N. Am. Benthol. Soc. 27:509-520.
DOI: https://doi.org/10.1899/07-119.1
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.
DOI: https://doi.org/10.1577/M06-039.1
Edited by
Fabrizio Stefani, National Research Council, Water Research Institute (CNR-IRSA), Brugherio, ItalyHow to Cite
Ghannam, Sally, and Edward P. Levri. 2023. “Periphyton Growth on Allochthonous Input in Streams May Lead to Higher Individual Growth Rates of the Invasive New Zealand Mud Snail (<em>Potamopyrgus antipodarum< Em>)”. Journal of Limnology 82 (1). https://doi.org/10.4081/jlimnol.2023.2092.
Copyright (c) 2023 The Author(s)
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
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