Ecology: Pomacea canaliculata is a dioecious (separate sexed) aquatic snail species. It is in the family Ampullaridae, or applesnails, which have both gills and lungs and an operculum (Rodriguez et al. 2019). Although P. canaliculata possesses gills and is aquatic, it is an obligate air breather, relying on its lungs to help it survive in water with low oxygen conditions, for egg laying, and during times of dormancy, in which it burrows in substrate using a siphon-like lobe as a snorkel (Rodriguez et al. 2019). Another terrestrial characteristic of this aquatic snail is its cleidoic calcareous (enclosed, semi-hard, calcium-rich shell) egg clutches that are laid above the water line (Yang et al. 2019). Unlike many aquatic snails whose eggs are susceptible to desiccation, eggs of Pomacea require a dry environment and are vulnerable to damage when exposed to water (Burks et al. 2010). Eggs are bright pink, and clutches can number over 200. When eggs begin to hatch the juveniles become visible and the outer shell becomes clear and white. Once hatched, the egg casings turn white and chalky in appearance (Yang et al. 2019; Hayes et al 2012). Females of this genus are known to store sperm, and P. canaliculata can store viable sperm for up to 140 days and are known to have multiple partners and exhibit multiple paternity in a single egg clutch in non-native populations (Yang et al. 2019; Burela and Martín 2011). Copulation time is lengthy (observed to range between 38 min-12.8 hr), and mating includes nuptial feeding, as males produce a secretion ingested by females (Burela and Martín 2011). Pomacea canaliculata, like other applesnails, feed primarily on macrophytes. However, they are omnivores and will opportunistically eat most organic matter, including other snails (Kwong et al. 2009, Manara et al. 2022).
References: (click for full references)
Burela, S., and P.R. Martín. 2011. Evolutionary and functional significance of lengthy copulations in a promiscuous apple snail,
Pomacea canaliculata (Caenogastropoda: Ampullariidae). Journal of Molluscan Studies 77(1):54-64. https://doi.org/10.1093/mollus/eyq035.
Burks, R.L., C.H. Kyle, and M.K. Trawick. 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.
Halwart, M. 1994. The golden apple snail Pomacea canaliculata in Asian rice farming systems: present impact and future threat. International Journal of Pest Management 40(2):199-206.
Hayes, K.A., R.H. Cowie, S.C. Thiengo, and E.E. Strong. 2012. Comparing apples with apples: clarifying the identities of two highly invasive Neotropical Ampullaridae (Caenogastropoda). Zoological Journal of the Linnean Society 166(4):723-753.
Hayes, K.A., R.C. Joshi, S.C. Thiengo, and R.H. Cowie. 2008. Out of South America: multiple origins of non-native apple snails in Asia. Diversity and Distributions 14(4):701-712. http://onlinelibrary.wiley.com/doi/10.1111/j.1472-4642.2008.00483.x/full.
Kwong, K., R.K.Y. Chan, and J. Qiu. 2009. The potential of the invasive snail Pomacea canaliculata as a predator of various life-stages of five species of freshwater snails. Malacologia 51(2):343-356.
Lowe, S., M. Browne, S. Boudjelas, and M. De Poorter. 2000. 100 of the World's Worst Invasive Alien Species: A selection from the gobal invasive species database. The Invasive Species Specialist Group (ISSG) a specialist group of the Species Survival Commission (SSC) of the World Conservation Union. www.issg.org/booklet.pdf.
Manara, E., V. Cambi, and P.R. Martín. 2022. Evaluating the combined use of feeding trials and a micrographic technique to study the natural diet of Pomacea canaliculata. Limnologica, p.126022.
Matsukura, K., M. Okuda, N.J. Cazzaniga, T. Wada. 2013. Genetic exchange between two freshwater apple snails, Pomacea canaliculata and Pomacea maculata invading East and Southeast Asia. Biological Invasions 15:2039-2048. https://doi.org/10.1007/s10530-013-0431-1.
Rawlings, T.A., K.A. Hayes, R.H. Cowie, and T.M. Collins. 2007. The identity, distribution, and impacts on non-native apple snails in the continental United States. BMC Evolutionary Biology 7:97. http://www.biomedcentral.com/1471-2148/7/97.
Rodriguez, C., G.I. Prieto, I.A. Vega, and A. Castro-Vazquez. 2019. Functional and evolutionary perspectives on gill structures of an obligate air-breathing, aquatic snail. PeerJ 7(e7342):1-34. https://doi.org/10.7717/peerj.7342.
Seuffert, M.E., and P.R. Martín. 2012. A lentic dweller in lotic habitats: the behavior of the invasive South American apple snail Pomacea canaliculata in flowing water. Aquatic Ecology 46(1):129-142.
Thompson, F.G. 1999. An identification manual for the freshwater snails of Florida.https://www.floridamuseum.ufl.edu/iz/resources/florida-snails/. Created on 07/08/2019. Accessed on 07/08/2019.
Wang, J., Y. Xing, Y. Dai, Y. Li, W. Xiang, J. Dai, and F. Xu. 2022. A novel gelatin-based sustained-release molluscicide for control of the invasive agricultural pest and disease vector Pomacea canaliculata. Molecules, 27(13), p.4268.
Yang, T., Wu, Z., and Lun, Z. 2013. The Apple Snail Pomacea canaliculata, a Novel Vector of the Rat Lungworm, Angiostrongylus cantonensis: its Introduction, Spread, and Control in China. Hawaii Journal of Medicine & Public Health 72(6):23-25.
Yang, Q., S. Liu, J. Li, D. Wang, and X. Yu. 2019. Microsatellite evidence for multiple paternity in non-native populations of Pomacea canaliculata (Caenogastropoda: Ampullariidae) in China. Aquatic Invasions 14(4):656-666. https://doi.org/10.3391/ai.2019.14.4.06.
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