Potamopyrgus antipodarum as a potential defender against swimmer's itch in European recreational water bodies-experimental study
Status PubMed-not-MEDLINE Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
29967728
PubMed Central
PMC6022732
DOI
10.7717/peerj.5045
PII: 5045
Knihovny.cz E-zdroje
- Klíčová slova
- Miracidia, Potamopyrgus antipodarum, Radix balthica, Trichobilharzia regenti, “Decoy effect”,
- Publikační typ
- časopisecké články MeSH
Swimmer's itch is a re-emerging human disease caused by bird schistosome cercariae, which can infect bathing or working people in water bodies. Even if cercariae fail after penetrating the human skin, they can cause dangerous symptoms in atypical mammal hosts. One of the natural methods to reduce the presence of cercariae in the environment could lie in the introduction of non-host snail species to the ecosystem, which is known as the "dilution" or "decoy" effect. The caenogastropod Potamopyrgus antipodarum-an alien in Europe-could be a good candidate against swimmer's itch because of its apparent resistance to invasion by European bird schistosome species and its high population density. As a pilot study on this topic, we have carried out a laboratory experiment on how P. antipodarum influences the infestation of the intermediate host Radix balthica (a native lymnaeid) by the bird schistosome Trichobilharzia regenti. We found that the co-exposure of 200 P. antipodarum individuals per one R. balthica to the T. regenti miracidia under experimental conditions makes the infestation ineffective. Our results show that a non-host snail population has the potential to interfere with the transmission of a trematode via suitable snail hosts.
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Allan BF, Langerhans RB, Ryberg WA, Landesman WJ, Griffin NW, Katz RS, Oberle BJ, Schutzenhofer MR, Smyth KN, De St Maurice A, Clark L, Crooks KR, Hernandez DE, McLean RG, Ostfeld RS, Chase JM. Ecological correlates of risk and incidence of West Nile virus in the United States. Oecologia. 2009;158:699–708. PubMed
Alonso A. Rating the impact of environmental degradation on benthic macroinvertebrates at the head of the river Henares. Ecosistemas. 2006;15:1–5.
Amen RI, Meuleman EA. Isolation of mother and daughter sporocysts of Trichobilharzia ocellata from Lymnaea stagnalis. Parasitology Research. 1992;78:265–266. doi: 10.1007/BF00931739. PubMed DOI
Angilletta Jr MJ. Estimating and comparing thermal performance curves. Journal of Thermal Biology. 2006;31:541–545. doi: 10.1016/j.jtherbio.2006.06.002. DOI
Arle J, Wagner F. Effects of anthropogenic salinisation on the ecological status of macroinvertebrate assemblages in the Werra River (Thuringia, Germany) Hydrobiologia. 2013;701:129–148. doi: 10.1007/s10750-012-1265-z. DOI
Begon M. Effects of host diversity on disease dynamics. In: Ostfeld RS, Keesing F, Eviner VT, editors. Infectious disease ecology: effects of ecosystems on disease and of disease on ecosystems. Princeton: Princeton University Press; 2008. pp. 12–29.
Berg MS Van Den, Coops H, Noordhuis R, Van Schie J, Simon J. Macroinvertebrate communities in relation to submerged vegetation in two Chara-dominated lakes. Hydrobiologia. 1997;342:143–150. doi: 10.1023/A:1017094013491. DOI
Blankespoor HD, Reimink RL. The control of swimmer’s itch in Michigan: past, present, future. Michigan Riparian. 1991;24:7–23.
Boycott AE. The habitats of fresh-water mollusca in Britain. Journal of Animal Ecology. 1936;5:116–186. doi: 10.2307/1096. DOI
Brzeziński T, Kołodziejczyk A. Distribution of Potamopyrgus antipodarum (Gray, 1843) in waters of the Wigry National Park and the effect of selected habitat factors on its occurrence. Folia Malacologica. 2001;9:125–135. doi: 10.12657/folmal.009.015. DOI
Carlsson R. The distribution of the gastropods Theodoxus fluviatilis (L.) and Potamopyrgus antipodarum (Gray) in lakes on the Åland Islands, southwestern Finland. Boreal Environment Research. 2000;5:187–195.
Chamot E, Toscani L, Rougemont A. Public health importance and risk factors for cercarial dermatitis associated with swimming in Lake Léman at Geneva, Switzerland. Epidemiology and Infection. 1998;120:305–314. doi: 10.1017/S0950268898008826. PubMed DOI PMC
Cianfanelli S, Lori E, Bodon M. Alien freshwater molluscs in Italy and their distribution. In: Gherardi F, editor. Biological invaders in inland waters: profiles, distribution, and threats. Springer Press; Dordrecht: 2007. pp. 103–121.
Cichy A, Faltynkova A, Żbikowska E. Cearcariae (Trematoda, Digenea) in European freshwater snails a checklist of records from over one hundred years. Folia Malacologica. 2011;19:165–189. doi: 10.2478/v10125-011-0023-6. DOI
Combes C, Moné H. Possible mechanisms of the decoy effect in Schistosoma mansoni transmission. International Journal for Parasitology. 1987;17:971–975. PubMed
Cort WW. Studies on schistosome dermatitis. IV. Further information on distribution in Canada and in the United States. American Journal of Hygiene. 1936;24:318–333. doi: 10.1093/oxfordjournals.aje.a118267. DOI
Dorgelo J. Density fluctuations in populations 1982–1986 and biological observations of Potamopyrgus jenkinsi in two trophically differing lakes. Aquatic Ecology. 1987;21:95–110. doi: 10.1007/BF02255459. DOI
Dubois JP. Effect of a sediment perturbation on the population of Radix peregra ovata in lake Annecy. abstract book of 2nd workshop on bird schistosomes, Annecy: 31.2003.
Ebbs ET, Loker ES, Davis NE, Flores V, Veleizan A, Brant SV. Schistosomes with wings: how host phylogeny and ecology shape the global distribution of Trichobilharzia querquedulae (Schistosomatidae) International Journal for Parasitology. 2016;46:669–677. doi: 10.1016/j.ijpara.2016.04.009. PubMed DOI
Eklu-Natey DT, Al-Khudri M, Gauthey D, Dubois JP, Wuest J, Vaucher C, Huggel H. Epidemiologie de la dermatite de baigneurs et morphologie de Trichobilharzia cf. ocellate dans le Lac Léman. Revue Suisse De Zoologie. 1985;92:939–953. doi: 10.5962/bhl.part.81924. DOI
Extence CA. The effect of drought on benthic invertebrate communities in a lowland river. Hydrobiologia. 1981;83:217–224. doi: 10.1007/BF00008269. DOI
Farahnak A, Essalat M. A study on cercarial dermatitis in Khuzestan province, south western Iran. BMC Public Health. 2003;3:35. doi: 10.1186/1471-2458-3-35. PubMed DOI PMC
Gaino E, Scoccia F, Lancioni T, Ludovisi A. The invader mudsnail Potamopyrgus antipodarum in the Tiber River basin (Central Italy) Italian Journal of Zoology. 2008;75:253–261. doi: 10.1080/11250000701885513. DOI
Gérard C, Hervé M, Hechinger RF. Long-term population fluctuations of the exotic New Zealand mudsnail Potamopyrgus antipodarum and its introduced aporocotylid trematode in northwestern France. Hydrobiologia. 2017 doi: 10.1007/s10750-017-3406-x. DOI
Gérard C, Le Lannic J. Establishment of a new host-parasite association between the introduced invasive species Potamopyrgus antipodarum (Smith) (Gastropoda) and Sanguinicola sp. Plehn (Trematoda) in Europe. Journal of Zoology. 2003;261:213–216. doi: 10.1017/S0952836903004084. DOI
Hall Jr RO, Tank JL, Dybdahl MF. Exotic snails dominate nitrogen and carbon cycling in a highly productive stream. Frontiers in Ecology and the Environment. 2003;1:407–411. doi: 10.1890/1540-9295(2003)001[0407:ESDNAC]2.0.CO;2. DOI
Hechinger RF. Faunal survey and identification key for the trematodes (Platyhelminthes: Digenea) infecting Potamopyrgus antipodarum (Gastropoda: Hydrobiidae) as first intermediate host. Zootaxa. 2012;3418:1–27.
Hertel J, Holweg A, Haberl B, Kalbe M, Haas W. Snail odour-clouds: spreading and contribution to the transmission success of Trichobilharzia ocellata (Trematoda: Digenea) miracidia. Oecologia. 2006;147:173–180. doi: 10.1007/s00442-005-0239-5. PubMed DOI
Hinz W, Boeters HD, Guenther A. On the freshwater mollusc fauna in the Spanish Province of Cuenca. Malakologische Abhandlungen. 1994;17:65–81.
Hoeffler DF. Cercarial dermatitis. Archives of Environmental Health. 1974;29:225–229. doi: 10.1080/00039896.1974.10666573. PubMed DOI
Horák P, Kolářová L. Bird schistosomes: do they die in mammalian skin? Trends in Parasitology. 2001;17:66–69. doi: 10.1016/S1471-4922(00)01770-0. PubMed DOI
Horák P, Kolářová L, Dvořák J. Trichobilharzia regenti n. sp. (Schistosomatidae, Bilharziellinae) a new nasal schistosome from Europe. Parasite. 1998;5:349–357. doi: 10.1051/parasite/1998054349. PubMed DOI
Horák P, Mikeš L, Lichtenbergová L, Skála V, Soldánová M, Brant SV. Avian schistosomes and outbreaks of cercarial dermatitis. Clinical Microbiology Reviews. 2015;28:165–190. doi: 10.1128/CMR.00043-14. PubMed DOI PMC
Horák P, Mikeš L, Rudolfova J, Kolářová L. Penetration of Trichobilharzia cercariae into mammals: dangerous or negligible event? Parasite. 2008;15:299–303. doi: 10.1051/parasite/2008153299. PubMed DOI
Hubendick B. The effectiveness of passive dispersal in Hydrobia jenkinsi. Zoologiska Bidrag Från Uppsala. 1950;28:93–504.
Hunter GW, Shillam DS, Trott OT, Howell EV. Schistosome dermatitis in Seattle, Washington. Journal of Parasitology. 1949;35:25–254. doi: 10.2307/3273299. PubMed DOI
Huňová K, Kašný M, Hampl V, Leontovyč R, Kuběna A, Mikeš L, Horák P. Radix spp.: identification of trematode intermediate hosts in the Czech Republic. Acta Parasitologica. 2012;57:273–284. doi: 10.2478/s11686-012-0040-7. PubMed DOI
Jarcho S, Van Burkalow A. A geographical study of swimmer’s itch in the United States and Canada. Geographical Review. 1952;42:212–226. doi: 10.2307/211386. DOI
Johnson PTJ, Lund PJ, Hartson RB, Yoshino TP. Community diversity reduces Schistosoma mansoni transmission, host pathology and human infection risk. Proceedings of the Royal Society B. 2009;276:1657–1663. doi: 10.1098/rspb.2008.1718. PubMed DOI PMC
Johnson PTJ, Preston DL, Hoverman JT, Henderson JS, Paull SH, Richgels KLD, Redmond MD. Species diversity reduces parasite infection through crossgenerational effects on host abundance. Ecology. 2012;93:56–64. PubMed
Johnson PTJ, Thieltges DW. Diversity, decoys and the dilution effect: how ecological communities affect disease risk. Journal of Experimental Biology. 2010;213:961–970. doi: 10.1242/jeb.037721. PubMed DOI
Jouet D, Ferté H, Depaquit J, Rudolfová J, Latour P, Zanella D, Kaltenbach ML, Léger N. Trichobilharzia spp. in natural conditions in Annecy Lake, France. Parasitology Research. 2008;103:51–58. PubMed
Kalinda C, Chimbari MJ, Mukaratirwa S. Effect of temperature on the Bulinus globosus—Schistosoma haematobium system. Infectious Diseases of Poverty. 2017;6:57. doi: 10.1186/s40249-017-0260-z. PubMed DOI PMC
King CH, Bertsch D. Historical perspective: snail control to prevent schistosomiasis. PLOS Neglected Tropical Diseases. 2015;9:e0003657. doi: 10.1371/journal.pntd.0003657. PubMed DOI PMC
King KC, Jokela J, Lively CM. Trematode parasites infect or die in snail hosts. Biological Letters. 2011;7:265–268. doi: 10.1098/rsbl.2010.0857. PubMed DOI PMC
Kolářová L, Horák P, Skírnisson K. Methodical approaches in the identification of areas with a potential risk of infection by bird schistosomes causing cercarial dermatitis. Journal of Helminthology. 2010;84:327–335. doi: 10.1017/S0022149X09990721. PubMed DOI
Kolářová L, Skírnisson K, Horák P. Schistosome cercariae as the causative agent of swimmer’s itch in Iceland. Journal of Helminthology. 1999;73:215–220. doi: 10.1017/S0022149X99000335. PubMed DOI
Lagrue C, Poulin R. Local diversity reduces infection risk across multiple freshwater host-parasite associations. Freshwater Biology. 2015;60:2445–2454. doi: 10.1111/fwb.12677. DOI
Leedom WS, Short LB. Cercaria pomaceae sp. n., a dermatitis-producing schistosome cercaria from Pomacea paludosa, the Florida apple snail. Journal of Parasitology. 1981;67:257–261. doi: 10.1017/S0022149X99000335. DOI
Lévesque B, Giovenazzo P, Guerrier P, Laverdiere D, Prud’Homme H. Investigation of an outbreak of cercarial dermatitis. Epidemiology and Infection. 2002;129:379–386. PubMed PMC
Lewin I, Smolinski A. Rare and vulnerable species in the mollusc communities in the mining subsidence reservoirs of an industrial area (The Katowicka Upland, Upper Silesia, Southern Poland) Limnologica. 2006;36:181–191. doi: 10.1016/j.limno.2006.04.002. DOI
Lichtenbergová L, Lassman H, Jones MK, Kolářová L, Horák P. Trichobilharzia regenti: host immune response in the pathogenesis of neuroinfection in mice. Experimental Parasitology. 2011;128:328–335. doi: 10.1016/j.exppara.2011.04.006. PubMed DOI
Lindblade KA. The epidemiology of cercarial dermatitis and its association with limnological characteristics of a northern Michigan Lake. Journal of Parasitology. 1998;84:19–23. doi: 10.2307/3284521. PubMed DOI
Loken BR, Spencer CR, Granath Jr WO. Prevalence and transmission of cercariae causing schistosome dermatitis in Flathead Lake, Montana. Journal of Parasitology. 1995;81:646–649. doi: 10.2307/3283870. PubMed DOI
Loker E, Hofkin B. Parasitology: a conceptual approach. Garland Science; New York: 2015. Chapter 9: the challenge of parasite control. 576p.
Macy RW. Studies on schistosome dermatitis in the Pacific Northwest. Northwest Medicine. 1952;51:947–950. PubMed
Marszewska A, Cichy A, Heese T, Żbikowska E. The real threat of swimmers’ itch in anthropogenic recreational water body of the Polish Lowland. Parasitology Research. 2016;115:3049–3056. doi: 10.1007/s00436-016-5060-z. PubMed DOI PMC
McCullough FS. The role of mollusciciding in schistosomiasis control. WHO/Schist/92.107 1992
Mehlhorn H. Encyclopedia of parasitology. Heidelberg: Springer; 2008.
Meuleman EA, Huyer AR, Mooij JH. Maintenance of the life cycle of Trichobilharzia ocellata via the duck Anas platyrhynchos and the pond snail Lymnaea stagnalis. Netherlands Journal of Zoology. 1984;34:414–417.
Mitchell CE, Reich PB, Tilman D, Groth JV. Effects of elevated CO2, nitrogen deposition, and decreased species diversity on foliar fungal plant disease. Global Change Biology. 2003;9:438–451. doi: 10.1046/j.1365-2486.2003.00602.x. DOI
Moffitt CM, James CA. Response of New Zealand mudsnails Potamopyrgus antipodarum to freezing and near-freezing fluctuating water temperatures. Freshwater Science. 2012;31:1035–1041. doi: 10.1899/11-160.1. DOI
Moore JW, Herbst DB, Heady WN, Carlson SM. Stream community and ecosystem responses to the boom and bust of an invading snail. Biological Invasions. 2012;14:2435–2446. doi: 10.1007/s10530-012-0240-y. DOI
Morley NJ. The role of the invasive snail Potamopyrgus antipodarum in the transmission of trematode parasites in Europe and its implication for ecotoxicological studies. Aquatic Sciences. 2008;70:107–114. doi: 10.1007/s00027-007-7052-7. DOI
Mouthon J, Dubois JP. Mollusc communities of the littoral zone of Annecy Lake (Savoie, France) International Journal of Limnology. 2001;37:267–276. doi: 10.1051/limn/2001023. DOI
Muñoz Antoli C, Marín A, Toledo R, Esteban JG. Effect of Echinostoma friedi (Trematoda: Echinostomatidae) experimental infection on longevity, growth and fecundity of juvenile Radix peregra (Gastropoda: Lymnaeidae) and Biomphalaria glabrata (Gastropoda: Planorbidae) snails. Parasitology Research. 2007;101:1663–1670. doi: 10.1007/s00436-007-0710-9. PubMed DOI
Múrria C, Bonada N, Prat N. Effects of the invasive species Potamopyrgus antipodarum (Hydrobiidae, Mollusca) on community structure in a small Mediterranean stream. Fundamental and Applied Limnology. 2008;171:131–143. doi: 10.1127/1863-9135/2008/0171-0131. DOI
Piechocki A, Wawrzyniak-Wydrowska B. Guide to freshwater and marine mollusca of Poland. Bogucki Publishing House; Poznań: 2016.
Pilz J, Eisels S, Disko R. Zerkariendermatitis (swimmer’s itch) Fallbericht einer Zerkariendermatitis durch Trichobilharzia (Digenea, Schistosomatidae) Der Hautarzt. 1995;46:335–338. doi: 10.1007/s001050050262. PubMed DOI
Pointier JP, David P, Jarne P. The biological control of the snail hosts of schistosomes: the role of competitor snails and biological invasions. In: Toledo R, Fried B, editors. Biomphalaria snails and larval Trematodes. Springer Press; New York: 2011. pp. 215–238.
Ponder WF. Potamopyrgus antipodarum—a Molluscan colonizer of Europe and Australia. The Journal of Molluscan Studies. 1988;54:271–285. doi: 10.1093/mollus/54.3.271. DOI
Radea C, Louvrou I, Economou-Amilli A. First record of the New Zealand mud snail Potamopyrgus antipodarum J.E. Gray 1843 (Mollusca: Hydrobiidae) in Greece—notes on its population structure and the associated microalgae. Aquatic Invasions. 2008;3:341–344. doi: 10.3391/ai.2008.3.3.10. DOI
Rempfer J, Livingstone DM, Blodau C, Forster R, Niederhauser P, Kipfer R. The effect of the exceptionally mild European winter of 2006–2007 on temperature and oxygen profiles in lakes in Switzerland: a foretaste of the future? Limnology and Oceanography. 2010;55:2170–2180. doi: 10.4319/lo.2010.55.5.2170. DOI
Richards DC, Cazier LD, Lester GT. Spatial distribution of three snail species, including the invader Potamopyrgus antipodarum, in a freshwater spring. Western North American Naturalist. 2001;61:375–380. doi: 10.1080/11250000701885513. DOI
Riley LA, Dybdahl MF, Hall Jr RO. Invasive species impact: asymmetric interactions between invasive and endemic freshwater snails. Journal of the North American Benthological Society. 2008;27:509–520. doi: 10.1899/07-119.1. DOI
Sapp KK, Loker ES. Mechanisms underlying digenean-snail specificity: role of miracidial attachment and host plasma factors. Journal of Parasitology. 2000;86:1012–1019. doi: 10.1645/0022-3395(2000)086[1012:MUDSSR]2.0.CO;2. PubMed DOI
Schniebs K, Gloer P, Vinarski MV, Hundsdoerfer AK. Intraspecific morphological and genetic variability in Radix balthica (Linnaeus, 1758) (Gastropoda: Basoommatophora: Lymnaeidae) with morphological comparison to other European Radix species. Journal of Conchology. 2011;40:657–678.
Simoes M. Distribution in Portugal of Potamopyrgus jenkinsi (Prosobranchia Hydrobiidae) Iberus. 1988;8:243–244.
Skírnisson K, Kolárová L. Swimmer’s itch in Landmannalaugar, Iceland. Laeknabladid. 2005;91:729–736. PubMed
Smyth JD, Halton DW. The physiology of Trematodes. 2nd edition Cambridge University Press; Cambridge: 1983.
Soldánová M, Selbach C, Kalbe M, Kostadinova A, Sures B. Swimmer’s itch: etiology, impact, and risk factors in Europe. Trends in Parasitology. 2013;29:65–74. doi: 10.1016/j.pt.2012.12.002. PubMed DOI
Soldánová M, Selbach C, Sures B. The early worm catches the bird? Productivity and patterns of Trichobilharzia szidati cercarial emission from Lymnaea stagnalis. PLOS ONE. 2016;11:e0149678. doi: 10.1371/journal.pone.0149678. PubMed DOI PMC
Soler J. Diversity and distribution of freshwater molluscs in the Community of Madrid (Spain) Graellsia. 2006;62:201–252. doi: 10.3989/graellsia.2006.v62.iExtra.119. DOI
Son MO, Nabozhenko MV, Shokhin IV. The Don River basin is a new stage of expansion of Potamopyrgus jenkinsi (Smith, 1889) (Gastropoda, Hydrobioidea) in Europe. Doklady Biological Sciences. 2008;419:129–130. doi: 10.1134/S0012496608020178. PubMed DOI
Sousa R, Guilhermino L, Antunes C. Molluscan fauna in the freshwater tidal area of the River Minho estuary, NW of Iberian Peninsula. Annales de Limnologie-International Journal of Limnology. 2005;41:141–147. doi: 10.1051/limn/2005009. DOI
Städler T, Frye M, Neiman M, Lively CM. Mitochondrial haplotypes and the New Zealand origin of clonal European Potamopyrgus, an invasive aquatic snail. Molecular Ecology. 2005;14:2465–2473. doi: 10.1111/j.1365-294X.2005.02603.x. PubMed DOI
Strzelec M, Krodkiewska M, Królczyk A. The impact of environmental factors on the diversity of gastropod communities in sinkhole ponds in a coal mining region (Silesian Upland, Southern Poland) Biologia. 2014;69:780–789. doi: 10.2478/s11756-014-0369-5. DOI
Strzelec M, Spyra A, Krodkiewska M. Freshwater snails of the sand-pits in Uppersilesia Industrial Area (Poland) Teka Komisji Ochrony i Kształtowania Środowiska Przyrodniczego. 2006;3:187–194.
Sullivan JT, Yeung JT. Incompatibility between miracidia of Schistosoma mansoni and Helisoma duryi occurs at two stages: penetration and intramolluscan establishment. Journal of Parasitology. 2011;97:743–745. doi: 10.1645/GE-2758.1. PubMed DOI
Thomsen MS, Wernberg T, Silliman BR, Josefson AB. Broad-scale patterns of abundance of non-indigenous soft-bottom invertebrates in Denmark. Helgoland Marine Research. 2009;63:159–167. doi: 10.1007/s10152-008-0142-7. DOI
Urbański J. Beitrage zur Kenntnis der Molluskenfauna der Wojewodschaft Poznań. II. Fragmenta Faunistica Musei Zoologici Polonici. 1938;3:439–467.
Wagner S. Mollusk population in the Main River near Muehlheim/Dietesheim, Germany. Mitteilungen Der Deutschen Malakozoologischen Gesellschaft. 2000;65:23–33.
Walter JE. A new snail in the Lake of Zurich Switzerland Potamopyrgus jenkinsi New Record Gastropoda Prosobranchia. Vierteljahrsschrift der Naturforschenden Gesellschaft in Zürich. 1980;125:197–200.
Żbikowska E. Is there a potential danger of “swimmer’s itch” in Poland. Parasitology Research. 2003;89:59–62. doi: 10.1007/s00436-002-0684-6. PubMed DOI
Żbikowska E, Nowak A. One hundred years of research on the natural infection of freshwater snails by trematode larvae in Europe. Parasitology Research. 2009;105:301–311. doi: 10.1007/s00436-009-1462-5. PubMed DOI
Żbikowska E, Wójcik AR, Grygon-Franckiewicz B. “Wysypka pływaków” (swimmer’s itch) - dermatoza o objawach chorobowych podobnych do zmian wywołanych przez pasożytnicze, alergogenne i jadowite stawonogi. In: Buczek A, Błaszak C, editors. Stawonogi w Medycynie. Liber; Lublin: 2002. pp. 229–237.
Żbikowski J, Żbikowska E. Invaders of an invader—trematodes in Potamopyrgus antipodarum in Poland. Journal of Invertebrate Pathology. 2009;101:67–70. doi: 10.1016/j.jip.2009.02.005. PubMed DOI
Zettler ML, Richard D. Freshwater molluscs from Corsica. Notated collections from summer 2003 with emphasis on Theodoxus fluviatilis. Malakologische Abhandlungen. 2004;22:3–16.
Zieritz A, Waringer J. Distribution patterns and habitat characterization of aquatic Mollusca in the Weidlingbach near Vienna, Austria. Archiv für Hydrobiologie. 2008;166:271–292. doi: 10.1127/lr/18/2008/271. DOI