Native and non-native records of the invasive freshwater apple snail Pomacea maculata Perry, 1810

Occurrence
Latest version published by Instituto de Ciencias Biológicas y Biomédicas del Sur (INBIOSUR) on Sept 15, 2026 Instituto de Ciencias Biológicas y Biomédicas del Sur (INBIOSUR)

Download the latest version of this resource data as a Darwin Core Archive (DwC-A) or the resource metadata as EML or RTF:

Data as a DwC-A file download 1,650 records in English (105 KB) - Update frequency: as needed
Metadata as an EML file download in English (56 KB)
Metadata as an RTF file download in English (49 KB)

Description

This dataset comprises 1650 records of the freshwater snail Pomacea maculata (Caenogastropoda: Ampullariidae), gathered from bibliographic sources, museum collections, human observations and field surveys conducted by the research team. Of these occurrences, 332 correspond to the native range, while 1318 belong to invaded areas.This species is native to South America; however, it has been introduced to other parts of the world through the aquarium trade and, particularly in Asia, as a food resource for human consumption. As an invasive species, Pomacea maculata may alter food-web structure and ecosystem functioning by competing with native species, consuming aquatic plants, and providing a novel prey source for native predators. Such invasions may also lead to shifts in feeding behavior among other organisms and provide new hosts for parasites, including the rat lungworm, Angiostrongylus cantonensis. By consuming macrophytes, invasive Pomacea species can modify entire aquatic ecosystems by driving shifts between alternative stable states.

Data Records

The data in this occurrence resource has been published as a Darwin Core Archive (DwC-A), which is a standardized format for sharing biodiversity data as a set of one or more data tables. The core data table contains 1,650 records.

This IPT archives the data and thus serves as the data repository. The data and resource metadata are available for download in the downloads section. The versions table lists other versions of the resource that have been made publicly available and allows tracking changes made to the resource over time.

Versions

The table below shows only published versions of the resource that are publicly accessible.

How to cite

Researchers should cite this work as follows:

Asgrizze V, Seuffert M E, Soria A L, Burela S, Martín P R (2026). Native and non-native records of the invasive freshwater apple snail Pomacea maculata Perry, 1810. Version 1.2. Instituto de Ciencias Biológicas y Biomédicas del Sur (INBIOSUR). Occurrence dataset. https://ipt.mincyt.gob.ar/resource?r=pmaculatainbiosur&v=1.2

Rights

Researchers should respect the following rights statement:

The publisher and rights holder of this work is Instituto de Ciencias Biológicas y Biomédicas del Sur (INBIOSUR). This work is licensed under a Creative Commons Attribution (CC-BY 4.0) License.

GBIF Registration

This resource has been registered with GBIF, and assigned the following GBIF UUID: d94f4dcb-ef30-4dea-bace-eb32fbe41f04.  Instituto de Ciencias Biológicas y Biomédicas del Sur (INBIOSUR) publishes this resource, and is itself registered in GBIF as a data publisher endorsed by GBIF Argentina.

Keywords

occurrence; Asia; Europe; Freshwater snail; Non-native species; North America; South America

Contacts

Valentina Asgrizze
  • Metadata Provider
  • Originator
  • Point Of Contact
Instituto de Ciencias Biológicas y Biomédicas del Sur - INBIOSUR
B8000 Bahía Blanca
Buenos Aires
AR
María Emilia Seuffert
  • Metadata Provider
  • Originator
  • Point Of Contact
  • Researcher
Instituto de Ciencias Biológicas y Biomédicas del Sur. INBIOSUR UNS-CONICET
  • San Juan 671
8000 Bahía Blanca
Buenos Aires
AR
  • 2914167217
Abril Lujan Soria
  • Originator
Instituto de Ciencias Biológicas y Biomédicas del Sur - INBIOSUR
Bahía Blanca
Buenos Aires
AR
Silvana Burela
  • Originator
Instituto de Ciencias Biológicas y Biomédicas del Sur - INBIOSUR
Bahía Blanca
Buenos Aires
AR
Pablo Rafael Martín
  • Metadata Provider
  • Originator
Instituto de Ciencias Biológicas y Biomédicas del Sur - INBIOSUR
Bahía Blanca
Buenos Airees
AR

Geographic Coverage

This resource includes records of Pomacea maculata from both its native range in South America and its introduced range in North America, Asia and Europe. In South America, data are concentrated in Argentina, Brazil, Bolivia, Paraguay, and Uruguay. In North America, most records are concentrated in the Florida Peninsula (USA), although additional occurrences have been reported from Arizona, Texas, Louisiana, Mississippi, Alabama, and Georgia. In Asia, records have been documented in Bangladesh, Cambodia, China, Indonesia, Israel, Japan, Malaysia, Myanmar, Pakistan, Philippines, Singapore, South Korea,Thailand, Taiwan, and Vietnam. In Europe, all known occurrences are restricted to the Ebro Delta, Spain.

Bounding Coordinates South West [-35.439, -111.939], North East [40.703, 137.85]

Taxonomic Coverage

The resource documents occurrences of the species Pomacea maculata (Perry, 1810), a freshwater gastropod of the family Ampullariidae, native to South America and invasive in North America, Asia and Europe.

Kingdom Animalia
Phylum Mollusca
Class Mesogastropoda
Order Gastropoda
Family Ampullariidae

Temporal Coverage

Start Date / End Date 1943-01-01 / 2026-05-05

Project Data

Freshwater gastropods are among the most threatened aquatic taxa globally, yet some species have become highly invasive pests, causing severe economic and ecological impacts. This doctoral thesis project aims to understand the mechanisms and environmental factors determining the geographic distribution of freshwater gastropods in Argentina using ecological niche modeling (ENM). The project evaluates the conservation status, bioclimatic niche, and future trends of native and vulnerable species, such as Pomacea scalaris, comparing its ecological niche with the invasive apple snails Pomacea canaliculata and Pomacea maculata. Additionally, it projects models the potential distribution of non-native invasive gastropods (such as Potamopyrgus antipodarum and Sinotaia quadrata) to identify key river basins at risk in Argentina.

Title Ecological Niche Modeling for the Analysis of Past, Present, and Future Distribution of Vulnerable and Invasive Freshwater Gastropods in Argentina
Funding Project PGI-UNS 24/ZB14: "Aplicación de modelos de nicho ecológico y distribución de especies para el estudio de gasterópodos dulciacuícolas nativos, invasores y vulnerables" (PI/Director: Dr. María Emilia Seuffert), Universidad Nacional del Sur (UNS). Project PGI-UNS 24/ZB44: "Las dos caras del género Pomacea: nicho ecológico, vulnerabilidad y potencial invasivo" (PI/Director: Dr. María Emilia Seuffert), Universidad Nacional del Sur (UNS).
Study Area Description The study area spans freshwater ecosystems across Argentina, with sampling campaigns and historical museum collection assessments focusing primarily on the provinces of Buenos Aires, Entre Ríos, Corrientes, Santa Fe, Misiones, Chaco, and Formosa. The analyses encompass native distributions, historical fossil records, and potential expansion areas across major South American river basins (e.g., La Plata Basin and southern Pampas streams).
Design Description The research design combines field sampling, museum collection curation, and spatial bioclimatic modeling: 1.Field Sampling & Curation: Occurrence records are retrieved from malacological collections (MACN, FCNyM-UNLP, FML, MNHN Uruguay, MNHN Paraguay) and field surveys across 40 sampling sites. Snails, empty shells, opercula, and egg masses are georeferenced and photographed under standardized protocols. 2. Conservation & Spatial Assessment: Geospatial analyses using GeoCAT are applied to calculate the Extent of Occurrence (EOO) and Area of Occupancy (AOO) following IUCN criteria. 3. Ecological Niche Modeling (ENM): Models are developed using MaxEnt (via the 'kuenm' R package) and WorldClim bioclimatic variables (1970–2000). Projections are performed for future climate scenarios (2041–2100 under various GCMs and SSPs) and past paleoclimate conditions (since the Last Glacial Maximum). 4.Comparative Niche Analysis: Principal Component Analyses (PCA) and niche equivalence/similarity tests are conducted using the 'ecospat' R package to compare bioclimatic tolerances between native vulnerable and invasive species.

The personnel involved in the project:

Sampling Methods

The records included in this dataset were obtained using multiple strategies. First, specimens deposited in collections from the La Plata Museum of Natural Sciences, the Argentine Museum of Natural Sciences and Museum of Zoology of the University of São Paulo, were consulted. In addition, georeferenced occurrence records were downloaded from iNaturalist, selecting observations classified as research grade. For bibliographic data, the scientific literature was searched using the terms “Pomacea maculata”, “Ampullaria insularum”, “Ampullaria amazonica”, "Pomacea insularum", “Pomacea amazonica” and “Pomacea gigas” to identify publications that reported occurrences of the species. Finally, data collected by the resource team during previous field surveys were included. Records lacking geographic coordinates were georeferenced whenever the site description was sufficiently precise. All coordinates were visually inspected in QGIS.

Study Extent The study area encompasses aquatic regions of South and North America, Asia and Europe, where Pomacea maculata has been reported. The environments considered include both natural and artificial freshwater bodies such as rivers, lagoons, streams, and canals.
Quality Control Records without verifiable geographic coordinates were discarded. Additionally, publications by the same authors, in which specimens were collected from the same locality, were excluded to avoid duplicate occurrence records. iNaturalist records were manually reviewed and filtered according to their validation status. Furthermore, iNaturalist records with photos in which the species could not be clearly identified were excluded. Additionally, records from Peru were excluded because Ramirez et al. 2020 demonstrated that these records correspond to Pomacea nobilis, another species within the genus.

Method step description:

  1. 1. Data acquisition from museums and biological collections. 2. Compilation of historical records obtained during previous field surveys conducted by the research team. 3. Download and review of iNaturalist observations. 4. Literature review and extraction of occurrence records. 5. Georeferencing and visual verification in QGIS. 6. Standardization according to the Darwin Core standard. 7. Taxonomic and geographic validation. 8. Final integration and curation of the dataset.

Bibliographic Citations

  1. Agudo-Padrón, A. I. (2020). Additions to the systematic inventory of non-marine molluscs occurring in the State of Santa Catarina/SC, central southern Brazil region. Advances in Environmental Studies, 4(1), 261–270. https://pdfs.semanticscholar.org/ee84/9ae0404b7e670b099853fe36fbb8244aec06.pdf
  2. Brola, T. R. (2021). Estrategias reproductivas de moluscos gasterópodos: Caracterización de las defensas de los huevos de Pomacea scalaris y Pomacea diffusa (Caenogasteropoda: Ampullariidae) [Tesis]. https://naturalis.fcnym.unlp.edu.ar/entities/publication/fee29b99-5e63-4a0b-8dec-3100cdba39e6
  3. Brola, T. R., Pasquevich, M. Y., Giglio, M. L., Fernández, P. E., Cocucci, A., Dreon, M. S., & Heras, H. (2026). Evolution of aquatic snails' defences resulted in clade-specific differences in egg toxicity, pigments and warning coloration. Proceedings of the Royal Society B: Biological Sciences, 293. https://ore.exeter.ac.uk/articles/journal_contribution/Evolution_of_aquatic_snails_defences_resulted_in_clade-specific_differences_in_egg_toxicity_pigments_and_warning_colouration/30329482?file=62980996
  4. Cantanhede, S. P. D., Fernandez, M. A., Mattos, A. C. D., Montresor, L. C., Silva-Souza, N., & Thiengo, S. C. (2014). Freshwater gastropods of the Baixada Maranhense Microregion, an endemic area for schistosomiasis in the State of Maranhão, Brazil: I – Qualitative study. Revista da Sociedade Brasileira de Medicina Tropical, 47, 79–85. https://dx.doi.org/10.5123/s2176-6223202301357
  5. César, I. I., Ocón, C., Paggi, A. C., Rodrigues Capítulo, A., Spaccesi, F. G., Tangorra, M., & Tassara, M. P. (2000). Diversidad de invertebrados bentónicos del Río de la Plata. Biología Acuática. https://sedici.unlp.edu.ar/handle/10915/69062
  6. Clavijo, C., & Scarabino, F. (2011). Taller “Ampullariid Model using Phylogenetics, Laboratory Inquiry and Field Investigations into Ecology and Distribution”. Sicardia. Boletín Electrónico de la Sociedad Malacológica del Uruguay, 2, 10. https://www.scielo.br/j/bjb/a/JzjbxddzPJMjDsRGyLjhHZx/?lang=en
  7. Coelho, P. R. S., Thiengo, S. C., de Mendonça, C. L. F., de Oliveira, N. M. T., dos Santos, S. B., Caldeira, R. L., & Geiger, S. M. (2024). Diversity of freshwater mollusks from Lake Pampulha, Municipality of Belo Horizonte, Minas Gerais, Brazil. Diversity, 16(4), 193. https://www.mdpi.com/1424-2818/16/4/193
  8. Coria, S. H. (1997). Microanatomía del sistema reproductor de Ampullaria insularum Orbigny 1835 (Mollusca: Gastropoda: Ampullariidae) [Tesis]. https://bibliotecadigital.exactas.uba.ar/download/seminario/seminario_nBIO000510_Coria.pdf
  9. Darrigran, G. A. (1994). Composición de la malacofauna litoral del estuario del Río de la Plata. Tankay. https://sedici.unlp.edu.ar/bitstream/handle/10915/153700/Documento_completo.pdf?sequence=1
  10. Darrigran, G., & Lagreca, M. (s. f.). Moluscos litorales del estuario del Río de la Plata – Argentina. https://naturalis.fcnym.unlp.edu.ar/bitstreams/81dedd63-ff34-4020-8ef4-3ef5f1d28a7c/download
  11. de Lucia, M., Victorero, A., & Gutierrez Gregoric, D. E. (2025). Actualización del inventario de moluscos dulceacuícolas en la Reserva Natural de Punta Lara (2022–2025) y cambios frente a alteraciones ambientales recientes.
  12. de Oliveira, J. L., de Vasconcelos, M. C., & dos Santos, S. B. (2017). Freshwater mollusks and environmental assessment of Guandu River. Biota Neotropica, 17(3), e20170342. https://www.academia.edu/download/83088438/1676-0611-bn-17-3-e20170342.pdf
  13. dos Santos Castro, L., da Silva, J. D. S. P., Montresor, L. C., & da Silva, J. P. (2023). Alterações metabólicas em Pomacea maculata experimentalmente infectada com Angiostrongylus cantonensis (Nematoda). Revista Foco, 16(6), e2399.
  14. Fernández, M. A., Santos, S. B. D., Silva, E. F. D., & Thiengo, S. C. (2023). Composição e distribuição de moluscos de água doce no bioma Pantanal, estado de Mato Grosso, Brasil. Revista Pan-Amazônica de Saúde, 14.
  15. Glasheen, P. M., Burks, R. L., Campos, S. R., & Hayes, K. A. (2020). First evidence of introgressive hybridization of apple snails (Pomacea spp.) in their native range. Journal of Molluscan Studies, 86(2), 96–103. https://academic.oup.com/mollus/article-abstract/86/2/96/5748093
  16. Glasheen, P. M., Calvo, C., Meerhoff, M., Hayes, K. A., & Burks, R. L. (2017). Survival, recovery, and reproduction of apple snails (Pomacea spp.) following exposure to drought conditions. Freshwater Science, 36(2), 316–324. https://www.journals.uchicago.edu/doi/abs/10.1086/691791
  17. Hayes, K. A., Cowie, R. H., Thiengo, S. C., & Strong, E. E. (2012). Comparing apples with apples: Clarifying the identities of two highly invasive Neotropical Ampullariidae (Caenogastropoda). Zoological Journal of the Linnean Society, 166(4), 723–753. https://academic.oup.com/zoolinnean/article-abstract/166/4/723/2627113
  18. Hylton Scott, M. I. (2014). Estudio morfológico y taxonómico de los ampulláridos de la República Argentina. ProBiota, Serie Documentos.
  19. Kyle, C. H., Plantz, A. L., Shelton, T., & Burks, R. L. (2013). Count your eggs before they invade: Identifying and quantifying egg clutches of two invasive apple snail species (Pomacea). PLOS ONE, 8(10), e77736. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0077736
  20. Lipps, E. (2006). Observaciones biológicas en la “Cueva de los Murciélagos”. Vuelta de Obligado, provincia de Buenos Aires, República Argentina. Physis C, 25(70), 421–448. https://vueltadeobligado.wordpress.com/wp-content/uploads/2009/04/cuevas-rnhvo-2006.pdf
  21. Mattos, A. C. D., Boaventura, M. F. F., Fernandez, M. A., & Thiengo, S. C. (2013). Larval trematodes in freshwater gastropods from Mato Grosso, Brazil: Diversity and host–parasite relationships. Biota Neotropica, 13, 34–38. https://www.scielo.br/j/bn/a/6rgyL67Dhfg37SSNh4mrnVb/?format=html&lang=en
  22. Moreira, L. D. L., Silva, E. F. D., Gomes, S. R., Mattos, A. C. D., Sousa, A. K. P. D., Silva, A. B. P. D., Pinto, M. C., & Thiengo, S. C. (2024). Public parks in the city of Rio de Janeiro, southeast Brazil, and the risk of parasitosis transmission by freshwater gastropods. Anais da Academia Brasileira de Ciências, 96(2), e20230707. https://www.scielo.br/j/aabc/a/Dmbv8Vxy8bSsRRxpVJvmgxj/?lang=en
  23. Mu, H., Sun, J., Heras, H., Chu, K. H., & Qiu, J. W. (2017). An integrated proteomic and transcriptomic analysis of perivitelline fluid proteins in a freshwater gastropod laying aerial eggs. Journal of Proteomics, 155, 22–30. https://www.sciencedirect.com/science/article/pii/S1874391917300040
  24. Pasquevich, M. Y., Dreon, M. S., & Heras, H. (2014). The major egg reserve protein from the invasive apple snail Pomacea maculata is a complex carotenoprotein related to those of Pomacea canaliculata and Pomacea scalaris. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 169, 63–71. https://www.sciencedirect.com/science/article/pii/S1096495913001966?casa_token=PgKZUiaED8cAAAAA:UhQK4eWm08DvvprdISwk_m10DvEwqvdpTgOmMj1iAxpWrA69U8t86K32cxapXqPSafYOzPHkkyhN
  25. Phoong, M. J. C., Hah, H. E., Rao, S. R., Yow, Y. Y., & Ratnayeke, S. (2018). Invasive apple snails in wetlands of Selangor, Malaysia: Species, distribution, and ecological associations. Journal of Tropical Biology & Conservation, 15, 43–60. https://www.researchgate.net/profile/Yoon-Yen-Yow/publication/342343835_Invasive_Apple_Snails_in_Wetlands_of_Selangor_Malaysia_Species_Distribution_and_Ecological_Associations/links/5eeedb0992851ce9e7f78749/Invasive-Apple-Snails-in-Wetlands-of-Selangor-Malaysia-Species-Distribution-and-Ecological-Associations.pdf
  26. Verrengia Guerrero, N. R., & Kesten, E. M. (1993). Levels of heavy metals in biota from the La Plata River. Environmental Toxicology and Water Quality, 8(3), 335–344. https://onlinelibrary.wiley.com/doi/abs/10.1002/tox.2530080310?casa_token=D-avdynhHBgAAAAA:BIN-2KMT0gPtmzreUurdms4jkFZNrpop-lhdCiIxwKh20XfoV93KCl4V-oHyMPQZY0QR400Qiz-UeDfP
  27. Watanabe, T. T., Hattori, G. Y., & Sant’Anna, B. S. (2015). Desiccation tolerance of two apple snails from the Amazon basin, Pomacea amazonica and Pomacea bridgesii. Amazonian Resources, 43–52. https://www.researchgate.net/profile/Bruno-Santanna/publication/284644502_Desiccation_Tolerance_of_Two_Apple_Snails_from_the_Amazon_Basin_Pomacea_amazonica_and_Pomacea_bridgesii/links/65522aae3fa26f66f4fdd696/Desiccation-Tolerance-of-Two-Apple-Snails-from-the-Amazon-Basin-Pomacea-amazonica-and-Pomacea-bridgesii.pdf
  28. Cowie, R., Hayes, K., Strong, E., Thiengo, S. C., Joshi, R. C., Cowie, R., & Sebastian, L. (2017). Biology and management of invasive apple snails. Joshi RC, Cowie R, Sebastian L. Non-native apple snails: systematics, distribution, invasion history and reasons for introduction. Neuva Ecija: Philippine Rice Research Institute, 3-32. https://www.cabidigitallibrary.org/doi/full/10.5555/20173354475
  29. Ab Hamid, S., Haron, A., Amali, N., & Othman, I. (2023) Snails (Mollusca) diversity and its distribution in various type of microhabitats. Journal of Tropical Resources and Sustainable Science, 11 , 23-29. https://doi.org/10.47253/jtrss.v11i2.1237
  30. Abejo, J. R. A., & Jumawan, J. H. (2023). A multifaceted study of Wawa River, Esperanza, Agusan del Sur, Philippines–aquatic macroinvertebrates, water quality, and soil particle size analysis. American Journal of Interdisciplinary Research and Innovation, 2(4), 36-46. https://www.academia.edu/download/125119999/1012.pdf
  31. Achatz, T. J., Chun, C. H., Young, M. A., Page, J., Rowe, M., Cooper, C., ... & Tkach, V. V. (2025). Detection of rat lungworms in invasive mollusks, Georgia, USA, 2024. Emerging Infectious Diseases, 31(9), 1852. https://pmc.ncbi.nlm.nih.gov/articles/PMC12407195/
  32. Al, M. A., Akhtar, A., Kamal, A. H. M., AftabUddin, S., Islam, M. S., & Sharifuzzaman, S. M. (2022). Assessment of benthic macroinvertebrates as potential bioindicators of anthropogenic disturbance in southeast Bangladesh coast. Marine Pollution Bulletin, 184, 114217. https://doi.org/10.1016/j.marpolbul.2022.114217
  33. Arabie, D. (2019). Implications of hemocyanin to the respiratory regime of the invasive apple snail, Pomacea maculata (Perry, 1810) [Master's thesis, University of Louisiana at Lafayette]. https://search.proquest.com/openview/fe47fd686b451e75d79728b6119a04b8/1?pq-origsite=gscholar&cbl=18750&diss=y
  34. Baloch, W. A. (2018). Country report (Pakistan) on non-native apple snails. https://www.academia.edu/download/94119017/20173354470.pdf
  35. Banerjee, P., Dey, G., Maity, J. P., Stewart, K. A., Sharma, R. K., Chan, M. W., ... & Chen, C. Y. (2024). The unseen invaders: Tracking phylogeographic dynamics and genetic diversity of cryptic Pomacea canaliculata and P. maculata (Golden apple snails) across Taiwan. Ecology and Evolution, 14(4), e11268. https://doi.org/10.1002/ece3.11268
  36. Barbitta, D. (2017). Distribución y modelado global del nicho fundamental del caracol invasor Pomacea maculata (Perry, 1810) (Mollusca, Gasteropoda) [Tesis de licenciatura, Universidad de la República].
  37. Barnes, M. A., Fordham, R. K., Burks, R. L., & Hand, J. J. (2008). Fecundity of the exotic applesnail, Pomacea insularum. Journal of the North American Benthological Society, 27(3), 738-745. https://doi.org/10.1899/08-013.1
  38. Barrus, N. T., Drumheller, D., Cook, M. I., et al. (2023). Life history responses of two co-occurring congeneric apple snails (Pomacea maculata and P. paludosa) to variation in water depth and metaphyton total phosphorus. Hydrobiologia, 850, 841–860. https://doi.org/10.1007/s10750-022-05128-9
  39. Berrondo-Madrid, R., Vera, P., Gallardo, B., & Vilà, M. (2022). Stopping winter flooding of rice fields to control invasive snails has no effect on waterbird abundance at the landscape scale. Frontiers in Ecology and Evolution, 9, 688325 https://doi.org/10.3389/fevo.2021.688325
  40. Burkett-Cadena, N. D., & Unnasch, T. R. (2013). Apple snails and tiger mosquitoes: A curious association between two invasive species in Florida, USA. In Entomology 2013, 61st Annual Meeting of the Entomological Society of America. Austin Convention Center, Austin, Texas.
  41. Burks, R. L., Kyle, C. H., & Trawick, M. K. (2010). Pink eggs and snails: field oviposition patterns of an invasive snail, Pomacea insularum, indicate a preference for an invasive macrophyte. Hydrobiologia, 646(1), 243-251. https://doi.org/10.1007/s10750-010-0167-1
  42. Céspedes, V., Berrondo-Madrid, R., Picazo, F., Vilà, M., Rubio, C., García, M., ... & Gallardo, B. (2024). Massive decline of invasive apple snail populations after blue crab invasion in the Ebro River, Spain. Biological Invasions, 26(8), 2387-2395. https://doi.org/10.1007/s10530-024-03334-1
  43. Cowie, R., Hayes, K., Strong, E., Thiengo, S. C., Joshi, R. C., Cowie, R., & Sebastian, L. (2017). Biology and management of invasive apple snails. In R. C. Joshi, R. Cowie, & L. Sebastian (Eds.), Non-native apple snails: systematics, distribution, invasion history and reasons for introduction (pp. 3-32). Neuva Ecija: Philippine Rice Research Institute.
  44. Crichton, L. T. (2020). Abundance and distribution of the non-native apple snail, Pomacea maculata, in a restored wetland of an urban lake [Master's thesis, University of Central Florida].
  45. Do Van Tu, N. P. N., & Joshi, R. C. (2018). Invasive apple snails (Pomacea spp.) in Vietnam: Short review. https://www.deltamed.org/wp-content/uploads/2023/07/1521173863_invasive-apple-snails-pomacea-in-vietnam.pdf
  46. Dodd, S. R., Haynie, R. S., Williams, S. M., & Wilde, S. B. (2016). Alternate food-chain transfer of the toxin linked to avian vacuolar myelinopathy and implications for the endangered Florida snail kite (Rostrhamus sociabilis). The Journal of Wildlife Diseases, 52(2), 335-344. https://doi.org/10.7589/2015-03-061
  47. Dorn, N. J., & Hafsadi, M. (2016). Native crayfish consume more non-native than native apple snails. Biological Invasions, 18(1), 159-167. https://doi.org/10.1007/s10530-015-0998-9
  48. Drumheller, D. K., Cook, M. I., & Dorn, N. J. (2021). Direct chemical inhibition responsible for displacement of a native herbivore by an invasive congener. https://doi.org/10.21203/rs.3.rs-186320/v1
  49. Gilioli, G., Schrader, G., Carlsson, N., Van Donk, E., Van Leeuwen, C. H., Martín, P. R., ... & Vos, S. (2017). Environmental risk assessment for invasive alien species: a case study of apple snails affecting ecosystem services in Europe. Environmental Impact Assessment Review, 65, 1-11. https://doi.org/10.1016/j.eiar.2017.03.008
  50. Gnanasegaram, M. (2015). Comparative life cycle studies of Pomacea maculata and Pomacea canaliculata on rice (Oryza sativa). Pakistan Journal of Agricultural Sciences. http://www.pakjas.com.pk/
  51. Greufe, C., Ferrara, A., & Whitaker, J. (2024). Population genetic structure of invasive apple snails Pomacea maculata in Louisiana. Aquatic Ecology, 58(2), 487-500. https://doi.org/10.1007/s10452-024-10085-7
  52. Gutierre, S. M., Darby, P. C., Valentine-Darby, P. L., Mellow, D. J., Therrien, M., & Watford, M. (2019). Contrasting patterns of Pomacea maculata establishment and dispersal in an Everglades wetland unit and a central Florida lake. Diversity, 11(10), 183. https://doi.org/10.3390/d11100183
  53. Hansen, C. (2021). Effects of water flow on a wetland macroinvertebrate community [Master's thesis, Florida Atlantic University].
  54. Horn, K. C., Johnson, S. D., Boles, K. M., Moore, A., Siemann, E., & Gabler, C. A. (2008). Factors affecting hatching success of golden apple snail eggs: effects of water immersion and cannibalism. Wetlands, 28(2), 544-549. https://doi.org/10.1672/07-11.1
  55. Hui, T. H. (2019). Bi-coloured arboreal ants apparently feeding on eggs of apple snail.Singapore Biodiversity Records, 2019, 166–167. https://lkcnhm.nus.edu.sg/wp-content/uploads/sites/11/app/uploads/2019/01/sbr2019_166-167.pdf
  56. Li, J., Gao, J., & Chu, C. (2025). Identification of apple snails from other snails in snail food with quantitative PCR based on TaqMan-MGB probe. Journal of Food Composition and Analysis, 108508 https://doi.org/10.1016/j.jfca.2025.108508
  57. Ling, J., Li, T., Liu, Y., Chen, S., Fang, W., Zhao, S., & Jiang, Y. (2025). Molecular identification and population genetics of the invasive Pomacea spp. in Dali Bai Autonomous Prefecture. Chinese Journal of Schistosomiasis Control, 37(6), 626. https://www.zgxfzz.com/EN/Y2025/V37/I6/626
  58. Lucero, J. M., & Wilson, B. E. (2023). Regional expansion and chemical control for invasive apple snails (Pomacea maculata) in Louisiana rice and crawfish production systems. Crop Protection, 164, 106127. https://doi.org/10.1016/j.cropro.2022.106127
  59. Machado-Stredel, F., Atauchi, P. J., Nuñez-Penichet, C., Cobos, M. E., Osorio-Olvera, L., Khalighifar, A., Peterson, A. T., & Fletcher, R. J. (2024). The roles of abiotic and biotic factors in driving range shifts: An invasive Pomacea snail facilitates Rostrhamus sociabilis (Snail Kite) northward range expansion. Ornithology, 141(3), ukae022. https://doi.org/10.1093/ornithology/ukae022
  60. Martin, C. W., Bahya, K. M., & Valentine, J. F. (2012). Establishment of the invasive island apple snail Pomacea insularum (Gastropoda: Ampullaridae) and eradication efforts in Mobile, Alabama, USA. Gulf of Mexico Science, 30(1), 5. https://doi.org/10.18785/goms.3001.05
  61. Martin, C. W., & Valentine, J. F. (2014). Tolerance of embryos and hatchlings of the invasive apple snail Pomacea maculata to estuarine conditions. Aquatic Ecology, 48(3), 321-326. https://doi.org/10.1007/s10452-014-9486-z
  62. Marzolf, N. S., Shivers, S. D., Golladay, S. W., & Covich, A. P. (s.f.). Is environmental calcium availability limiting dispersal of an invasive snail in Lake Seminole and associated smaller lakes? https://www.researchgate.net/profile/Stephen_Golladay/publication/281825745_Abiotic_Effects_on_Spatial_Distribution_and_Abundance_of_Two_Highly_Invasive_Species_in_a_Novel_Lake_Ecosystem/links/5717a07308ae30c3f9f16f6c.pdf
  63. Matsukura, K. (2025). Recent range expansion of apple snails in East Asia and novel countermeasures. Japan Agricultural Research Quarterly: JARQ, 59(4), 245-252. https://doi.org/10.6090/jarq.24S26
  64. McAskill, S. C. (2015). Interactive effects of environmental stressors and the invasive apple snail, Pomacea maculata, on tapegrass, Vallisneria americana [Master's thesis, Florida Gulf Coast University].
  65. McMahon, R. F. (2024). Invasive fresh water molluscs in Texas. Texas Journal of Science, 76(1). https://doi.org/10.32011/txjsci_76_1_TDS1
  66. Meza-Lopez, M. M., & Siemann, E. (2015). Experimental test of the invasional meltdown hypothesis: an exotic herbivore facilitates an exotic plant, but the plant does not reciprocally facilitate the herbivore. Freshwater Biology, 60(7), 1475-1482. https://doi.org/10.1111/fwb.12582
  67. Morrison, W. E., & Hay, M. E. (2011). Feeding and growth of native, invasive and non-invasive alien apple snails (Ampullariidae) in the United States: invasives eat more and grow more. Biological Invasions, 13(4), 945-955. https://doi.org/10.1007/s10530-010-9881-x
  68. Mutchler, M. J., Nemecek, M. S., & Robbins, M. B. (2025). Patterns and demography of Limpkin (Aramus guarauna) vagrancy in the 21st century United States. The Wilson Journal of Ornithology, 137(4), 563-577. https://doi.org/10.1080/15594491.2025.2529110
  69. Ng, T. H., Tan, S. K., & Low, M. E. Y. (2014). Singapore Mollusca: 7. The family Ampullariidae (Gastropoda: Caenogastropoda: Ampullarioidea). Nature in Singapore, 7, 31-47. https://www.science.nus.edu.sg/wp-content/uploads/sites/11/2024/02/2014nis031-047.pdf
  70. Nguyen, J. A., Tolley-Jordan, L., Slayton, A. P., Richardson, B. M., & Rosser, T. G. (2025). First report of a trematode infection in an invasive population of Pomacea maculata: Evidence of a phaneropsolid (Trematoda: Microphalloidea) and recommended methods for surveillance. Parasitology International, 103203. https://doi.org/10.1016/j.parint.2025.103203
  71. Nigar Alkan, & Ali Alkan. (2023). Elemental compositions of Rapana venosa (Mollusca: Muricidae) from the eastern Black Sea region of Turkey: Toxicology health risk assessment. Analytical Letters, 56(3), 504-516. https://doi.org/10.1080/00032719.2022.2081334
  72. Olivier, H. M., Jenkins, J. A., Berhow, M., & Carter, J. (2016). A pilot study testing a natural and a synthetic molluscicide for controlling invasive apple snails (Pomacea maculata). Bulletin of Environmental Contamination and Toxicology, 96(3), 289-294. https://doi.org/10.1007/s00128-015-1709-z
  73. Ostrom, A. S., & Chesnes, T. C. (2014). An assessment of submersion as a mechanical control technique of Pomacea maculata eggs in southern Florida, USA. Natural Resources and Conservation, 2, 6-10. 10.13189/nrc.2014.020102
  74. Panchot, W., Siriwut, W., Thaweepworadej, P., & Kolasartsanee, I. (2025). Damaging potential to rice crops of the invasive apple snail (Pomacea maculata) and the native Thai apple snail (Pila celebensis) under changing temperature conditions in Thailand. Climate Change Ecology, 10, 100096. https://doi.org/10.1016/j.ecochg.2025.100096
  75. Paylangco, J. C. C., Gamalinda, E. F., Seroy, R. A., & Jumawan, J. C. (2020). Assessment of macroinvertebrates as bioindicators of water quality in the littoral zone of Lake Mainit, Philippines. Asian Journal of Biological and Life Sciences, 9(3), 371-378. 10.5530/ajbls.2020.9.56
  76. Pérez-Méndez, N., Alcaraz, C., Bertolero, A., Català-Forner, M., Garibaldi, L. A., González-Varo, J. P., Rivaes, S., & Martínez-Eixarch, M. (2022). Agricultural policies against invasive species generate contrasting outcomes for climate change mitigation and biodiversity conservation. Proceedings of the Royal Society B: Biological Sciences, 289(1985), 20221081. https://doi.org/10.1098/rspb.2022.1081
  77. Pierre, S. M., Quintana-Ascencio, P. F., Boughton, E. H., & Jenkins, D. G. (2017). Dispersal and local environment affect the spread of an invasive apple snail (Pomacea maculata) in Florida, USA. Biological Invasions, 19(9), 2647-2661. https://doi.org/10.1007/s10530-017-1474-5
  78. Prabhakaran, G., Bhore, S. J., & Ravichandran, M. (2017). Development and evaluation of poly herbal molluscicidal extracts for control of apple snail (Pomacea maculata). Agriculture, 7(3), 22. https://doi.org/10.3390/agriculture7030022
  79. Prabhakaran, G., Bhore, S., & Ravichandran, M. (2019). Development of a bait carrier material for apple snail (Pomacea maculata) based on its feed preferences using snail attractant tracking device. Journal of Natural Science, Biology and Medicine, 10(1), 8-15. https://www.researchgate.net/profile/Subhash-Bhore/publication/330852937_Development_of_a_bait_carrier_material_for_apple_snail_Pomacea_maculata_based_on_its_feed_preferences_using_snail_attractant_tracking_device/links/5c6d077c92851c1c9deebd97/Development-of-a-bait-carrier-material-for-apple-snail-Pomacea-maculata-based-on-its-feed-preferences-using-snail-attractant-tracking-device.pdf
  80. Qvarnstrom, Y., Bishop, H. S., & da Silva, A. J. (2013). Detection of rat lungworm in intermediate, definitive, and paratenic hosts obtained from environmental sources. Hawai'i Journal of Medicine & Public Health, 72(6 Suppl 2), 63–69. https://pmc.ncbi.nlm.nih.gov/articles/PMC3689491/
  81. Robertson, S. M. (2012). Potential threats of the exotic apple snail Pomacea insularum to aquatic ecosystems in Georgia and Florida. https://openscholar.uga.edu/record/14274
  82. Rosas, E. G., Bashara, C., Christie, D., Barnes, M. A., & Burks, R. L. (2025). Winning the shell game: environmental DNA (eDNA) confirms local control of the invasive apple snail, Pomacea maculata. Management of Biological Invasions, 16(2), 397-410. https://doi.org/10.3391/mbi.2025.16.2.05
  83. Rosli, N. A. M., Ismail, S. I., Nasir, N. M., Zainol, M., & Mokhtar, A. S. (2025). Field assessment of plant growth performance and residue persistence of saponin-based molluscicide formulations.
  84. Srijad, S., Sang-in, V., Pilapang, K., & Yomla, R. (2025). The effect of different periods of aestivation on recovery and nutritional composition of apple snail (Pomacea sp.). International Journal of Agricultural Technology, 21(4), 1479-1490. https://doi.org/10.63369/ijat.2025.21.4.1479-1490
  85. Teem, J. L., Qvarnstrom, Y., Bishop, H. S., da Silva, A. J., Carter, J., White-McLean, J., & Smith, T. (2013). The occurrence of the rat lungworm, Angiostrongylus cantonensis, in nonindigenous snails in the Gulf of Mexico region of the United States. Hawai'i Journal of Medicine & Public Health, 72(6 Suppl 2), 11. https://pmc.ncbi.nlm.nih.gov/articles/PMC3689474/
  86. Torres, O., Serrat, X., Sans, F. X., & Nogués, S. (2024). Manejo de malas hierbas en arrozales con presencia de caracol manzana en el Delta del Ebro. Revista de Ciências Agrárias, 47(1), 151-155. https://doi.org/10.19084/rca.34967
  87. Tookhy, N. A., Nur-Mahiza, M. I., Busayo Ibitoye, E., Lokman, H. I., & Shakhes, S. A. (2025). Freshwater snails in Malaysia: Diversity, roles in trematode transmission, and agricultural impacts. Pertanika Journal of Tropical Agricultural Science, 48(4). https://doi.org/10.47836/pjtas.48.4.09
  88. Underwood, E. (2018). Investigation of the population genetic structure, salinity tolerance, and occurrence of a parasite in the island apple snail, Pomacea maculata, in South Carolina, USA [Master's thesis, College of Charleston].
  89. Valente, R., Robles, M. D. R., & Diaz, J. I. (2020). Gastropods as intermediate hosts of Angiostrongylus spp. in the Americas: bioecological characteristics and geographical distribution. Memórias do Instituto Oswaldo Cruz, 115, e200236. https://doi.org/10.1590/0074-02760200236
  90. Wei, R., Xie, H. F., Wu, C. D., Hu, J., & Du, Y. Z. (2025). Impacts of climate change on the potential habitat suitability of Pomacea canaliculata and Pomacea maculata in East Asia. Zoological Studies, 64(56). https://doi.org/10.6620/ZS.2025.64-56
  91. Win, A. K., Naing, H. H., & Joshi, R. C. (2018). Managing the spread of invasive apple snails and possible utilization in aquaculture: A case in Myanmar. Fish for the People, 16(3), 38-40. http://hdl.handle.net/20.500.12066/4328
  92. Yang, Q. Q., Ip, J. C. H., Zhao, X. X., Li, J. N., Jin, Y. J., Yu, X. P., & Qiu, J. W. (2022). Molecular analyses revealed three morphologically similar species of non‐native apple snails and their patterns of distribution in freshwater wetlands of Hong Kong. Diversity and Distributions, 28(1), 97-111. https://doi.org/10.1111/ddi.13443
  93. Yap, C. K., & Al-Mutairi, K. A. (2025). Tissue-specific nickel accumulation and detoxification in Pomacea insularum: A biomonitoring tool for freshwater ecosystems. Polish Journal of Environmental Studies. https://doi.org/10.15244/pjoes/204564
  94. Yi, X. L., Liu, J., Cao, M. L., Xiong, J., Deng, Y. P., Wang, H. M., ... & Yang, H. (2024). Population genetics and genetic variation of Pomacea canaliculata (Gastropoda: Ampullariidae) in China revealed by sequence analyses of three mitochondrial genes. Ecology and Evolution, 14(1), e10836. https://doi.org/10.1002/ece3.10836
  95. Ramírez, R., Solis, M., Ampuero, A., Morín, J., Jimenez-Vasquez, V., Ramirez, J. L., ... & Shiga, B. (2020). Identificación molecular y relaciones evolutivas de Pomacea nobilis, base para la autenticación específica del churo negro de la Amazonia peruana. Revista peruana de biología, 27(2), 139-148. 10.15381/rpb.v27i2.17875
  96. Fan, J., Ma, Y., Xia, Y., Li, W., Lin, C., Liu, J., ... & Lan, T. (2026). Large-scale mitochondrial DNA analysis unravels the global invasion patterns of Pomacea snails (Gastropoda, Caenogastropoda, Ampullariidae). NeoBiota, 109, 1-24. https://neobiota.pensoft.net/article/189265/download/pdf/

Additional Metadata

Purpose
Alternative Identifiers d94f4dcb-ef30-4dea-bace-eb32fbe41f04
https://ipt.mincyt.gob.ar/resource?r=pmaculatainbiosur