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Planorbidae
Planorbidae
Planorbidae
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For "ramshorn snails" in the aquarium trade, some but not all of which are planorbids, see Ramshorn snail.

Planorbidae
Helicorbis australiensis
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Mollusca
Class: Gastropoda
Superorder: Hygrophila
Superfamily: Lymnaeoidea
Family: Planorbidae
Rafinesque, 1815[1]
Genera

See text

Diversity[2]
About 250 freshwater species
Synonyms
  • Laevapicidae Hannibal, 1914
  • Laevapicinae Hannibal, 1914

Planorbidae, common name the ramshorn snails or ram's horn snails, is a family of air-breathing freshwater snails, aquatic pulmonate gastropod molluscs. Unlike most molluscs, the blood of ram's horn snails contains iron-based hemoglobin instead of copper-based hemocyanin.[3] As a result, planorbids are able to breathe oxygen more efficiently than other molluscs. The presence of hemoglobin gives the body a reddish colour. This is especially apparent in albino animals.

Being air breathers like other Panpulmonata, planorbids do not have gills, but instead, have a lung. The foot and head of planorbids are rather small, while their thread-like tentacles are relatively long. Many of the species in this family have coiled shells that are planispiral, in other words, the shells are more or less coiled flat, rather than having an elevated spire as is the case in most gastropod shells. Although they carry their shell in a way that makes it appear to be dextral, the shell of coiled planorbids is in fact sinistral in coiling, but is carried upside down, which makes it appear to be dextral.

Description

[edit]
Apical, apertural and umbilical view of the shell of Biomphalaria tenagophila. Scale bar is 3 mm.

The shells of most species in this family are disk-like or button-like, being coiled in one plane, although several groups have shells that are more higher-spired, and some are limpet-like. [4]

All coiled shell Planorbidae are sinistral in their shell coiling, as is proved by their internal anatomy (the respiratory and the genital orifice are situated on the left side), however the animals carry their shells with what would normally be the ventral (i.e. umbilical) surface uppermost, and because of this, the shells appear to be dextral. Planorbids were once thought to have dextral shells, and so species of this family were figured as if they had dextral shells. Although it is now understood that these species are sinistral in shell coiling, disk-like Planorbid shells are often still shown in illustrations oriented as if they were dextral. [4]

Most species of coiled planorbids have a rather thin and moderately smooth shell, although more distinct sculpture such as a keel occurs in, and is diagnostic of, certain species. In the flat, keeled species, the whorls tend to overlap. Nearly all shells are composed of growth lines. [4]

The aperture has a sharp outer lip. A peristome can be present, but often the lip is not thickened nor reflected. Those planorbid species which have a high-spired shell may have a narrow umbilicus, but frequently this is covered by callus. [4]

In height most species vary between 6 mm and 6 cm, however, disk-like shells are usually less than about 2 cm in maximum dimension. [4]

Like all pulmonate aquatic snails, ramshorn shells do not have an operculum to close the shell aperture. [4]

Sinistral shells

[edit]
Planorbarius corneus. View of the sunken spire (held facing downwards in life)
Planorbarius corneus. View of the umbilicus (held uppermost in life)

Flat-coiled planorbid gastropod shells are hard to understand in terms of their coiling and orientation. Many of the shells of species in this family are almost planispiral in coiling such that one side of the shell often looks rather like the other side, but it is important to bear in mind that nonetheless there is an umbilical side and a spire side of the shell. The shells of planorbids are sinistral on close inspection, despite the fact that most species carry the shell as if it were a normal dextral shell.[4]

The side of the shell which is in fact the spire (a sunken spire) faces down in the living animal, contrary to what is the case in almost all other shelled gastropods. Because the shell is carried "upside down" like this, the aperture of the shell is angled to face downwards also, so the aperture faces towards the spire, not away from it. and the umbilicus faces upwards. The spire of the shell is quite sunken in many species. [4]

The umbilicus of the shell is very wide and shallow, and faces upwards. In some species the umbilicus is not as deeply "dished" as the sunken spire, so it may be hard to tell one from the other without close inspection. [4]

Distribution and habitat

[edit]

Species in this family occur worldwide.[5] Most species of planorbids live only in fresh water, such as ponds, lakes, and slow moving rivers. However, some species are known to tolerate conditions such as brackish water or sewage.[4]

Geological history

[edit]

Ancestors of ramshorn snails are known with certainty since the Jurassic period, but there are a few possible earlier occurrences starting in the Late Devonian.[6]

Taxonomy

[edit]
Albino planorbid clearly shows the reddish-colored body tissues due to the pigment hemoglobin

The following genera are recognised in the family Planorbidae:[7]

Planorbidae incertae sedis:

References

[edit]
[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Planorbidae

View on Grokipedia
from Grokipedia
Planorbidae is a family of air-breathing freshwater snails in the superfamily Planorboidea of the order Hygrophila, class , phylum . These pulmonate gastropods, commonly known as ramshorn snails, are characterized by their coiled shells that are typically planispiral (flat-spiraled like a ram's horn), discoidal, or sometimes patelliform (limpet-like), with a dextral (right-handed) coiling direction and often a blunt spire. The family comprises approximately 40 genera and around 250 species worldwide, exhibiting high diversity and , particularly in ancient lakes such as and . Planorbids are hermaphroditic, capable of self-fertilization, and reproduce at least once per year, often laying eggs in gelatinous masses. They inhabit a wide range of freshwater environments, including ponds, lakes, rivers, ditches, and temporary pools, and are distributed globally across all continents except , with notable concentrations in tropical and temperate regions. Ecologically, these snails serve as detritivores and grazers on and , helping to regulate algal in aquatic ecosystems, while their red blood, containing rather than , aids in oxygen uptake in low-oxygen waters. Several within Planorbidae, particularly in the genus Biomphalaria (e.g., Biomphalaria glabrata), act as intermediate hosts for schistosome parasites, transmitting diseases like (bilharzia) to humans and affecting in endemic areas of and the . The family's evolutionary history and phylogeny have been extensively studied since the mid-20th century, with key revisions highlighting their basal position among pulmonates and adaptations to freshwater life.

Biology

Morphology

Planorbidae, commonly known as ramshorn snails, exhibit a general typical of pulmonate gastropods, characterized by small to medium-sized individuals reaching up to 2-3 cm in shell diameter. These snails possess a soft-bodied morphology divided into a distinct head, a muscular foot for locomotion, and a visceral mass housing internal organs, all partially protected by the shell. The head features a small, rounded structure with two long, thread-like tentacles bearing eyes at their bases for sensory perception. The shell morphology is a hallmark of the family, consisting of coiled, discoidal or planispiral structures that are predominantly sinistral, meaning they coil left-handed when viewed from the apex. These shells have thin, often translucent walls composed primarily of calcium carbonate, with variations in whorl number ranging from 2 to 6 across species; for instance, Planorbis corneus typically displays 5-6 rapidly expanding whorls forming a tightly coiled disc. The aperture, or shell opening, varies in shape from oval to rounded, and the overall flattened spire contributes to the shell's low profile. This sinistral coiling is a defining trait, aligned with the internal anatomy where the respiratory and genital orifices are positioned on the left side, optimizing organ arrangement within the confined space. In terms of internal , the features a well-developed pulmonary cavity functioning as a for aerial , with gills entirely absent as an to air-breathing in freshwater. Unlike many aquatic mollusks that rely on , Planorbidae blood contains as the primary oxygen-transporting pigment, which efficiently binds oxygen and imparts a characteristic reddish hue to the soft tissues, particularly noticeable in translucent or albino specimens. The structure in species like Biomphalaria glabrata has evolved from ancestral pulmonate , enhancing respiratory efficiency in low-oxygen environments. Other notable soft parts include the , a chitinous, rasping structure with a taenioglossate arrangement of seven teeth per transverse row (one central and three pairs of laterals), adapted for scraping food from surfaces. The gonads are hermaphroditic, consisting of a single, lobulated embedded in the visceral mass, enabling simultaneous production of eggs and sperm as is typical in pulmonates. The discoidal shell shape aids , allowing these snails to maintain position in freshwater habitats.

Reproduction and life cycle

Members of the Planorbidae family are simultaneous hermaphrodites, possessing both male and female reproductive organs in a single , which enables them to function as both sexes during . This hermaphroditic condition allows for both self-fertilization, where a uses its own to fertilize its eggs, and cross-fertilization with another individual, though is preferred when possible to enhance . Internal fertilization occurs via an introvertible , with transferred directly into the partner's reproductive tract. Fertilization leads to the production of egg masses, which are deposited as gelatinous clusters on aquatic vegetation, submerged wood, rocks, or other surfaces. These masses typically contain 20–30 eggs per cluster, though numbers can vary by species and conditions; for example, in Helisoma trivolvis, each gel-like sack holds 5–20 eggs. The eggs are encased in a protective jelly matrix that hardens slightly after laying, providing a barrier against desiccation and predators. Hatching occurs after 1–3 weeks, depending on temperature and environmental factors, with embryos developing encapsulated within the mass until juveniles emerge. In Planorbarius corneus, hatching times range from 14–21 days, with a success rate of about 97%. The life cycle of planorbids features direct development without free-living larval stages, as juveniles hatch as miniature versions of adults, complete with a coiled shell and functional organs. Growth is rapid in favorable conditions, with snails reaching in 4–15 weeks; for instance, Planorbarius corneus matures at around 14–15 weeks post-hatching, when shell diameter reaches 7.5 mm. Adults typically live 1–2 years, producing multiple broods per season during warmer months, often with two reproductive peaks in spring and late summer. This iterative breeding supports high , with individuals like Planorbarius corneus laying up to 11 eggs per day and totaling over 4,000 eggs in their lifetime, facilitating rapid population expansions in nutrient-rich habitats. Parthenogenesis, an asexual reproductive mode, occurs in certain genera such as Helisoma, allowing unfertilized eggs to develop into viable offspring and enabling population establishment from single individuals. This capability complements sexual reproduction, providing flexibility in isolated or low-density environments.

Ecology

Habitat and distribution

Planorbidae exhibit a cosmopolitan distribution in freshwater systems worldwide, with species native to all continents except Antarctica and comprising approximately 250 species across about 40 genera. They are particularly diverse in tropical and subtropical regions, where genera such as Biomphalaria predominate; for instance, Biomphalaria species are widespread in sub-Saharan Africa and South America, often serving as intermediate hosts for schistosome parasites in these areas. In temperate zones, species like Planorbella and Gyraulus are common in North America and Eurasia, while some, such as Planorbarius corneus, have been introduced to North America and other regions outside their native European range through the aquarium trade and release with aquatic plants. These snails prefer still or slow-moving freshwater habitats, including , lakes, marshes, ditches, canals, and the vegetated edges of rivers, where they associate with aquatic vegetation and . They tolerate low dissolved oxygen levels characteristic of such environments, facilitated by air-breathing through a pulmonary sac (a modified ) and the presence of , which binds oxygen more efficiently than the found in many other gastropods. Optimal conditions generally include a range of 6 to 8 and water temperatures between 10°C and 30°C, though some species endure broader fluctuations in natural settings. Certain species demonstrate remarkable adaptability to ephemeral habitats; for example, members of the genus Gyraulus, such as Gyraulus rossmaessleri, can inhabit temporary pools and survive extended droughts through , retreating into their shells and sealing the to conserve moisture for several months. This resilience contributes to their presence in seasonal wetlands and intermittent water bodies across diverse regions.

Diet and feeding behavior

Planorbidae, commonly known as ramshorn snails, exhibit a primarily herbivorous-detritivorous diet, feeding on , decaying plant matter, and scraped from substrates using their , a chitinous ribbon-like structure equipped with teeth for rasping food. While mainly herbivorous, some display omnivorous tendencies by consuming small or carrion associated with . Feeding mechanisms in Planorbidae center on surfaces such as rocks, , and sediments with the to collect microbial films and organic . Activity patterns vary by species and context; for instance, groups of Biomphalaria alexandrina, a planorbid species, show bimodal crepuscular peaks, while individuals may be active throughout the night. As primary consumers in freshwater aquatic food webs, Planorbidae play a key role in cycling by breaking down , thereby facilitating the release of nutrients like and back into the . Their grazing reduces , influencing algal dynamics and supporting overall . Planorbidae interact trophically with predators such as , birds, and , which exert control on their populations through predation, while they compete with other species like Physidae for resources such as periphyton-covered substrates. In balanced ecosystems, Planorbidae efficiently control through , helping maintain ; however, in eutrophic waters, they can proliferate excessively, potentially exacerbating imbalances and becoming ecological pests.

Evolutionary history

Geological record

The fossil record of Planorbidae extends back to the late , with the earliest confirmed records from the early Permian (Kungurian stage, approximately 275 million years ago) in eastern , where Ludwig described two species tentatively assigned to the family. Possible precursors may trace to the late , but definitive ancestors appear in the Jurassic period (approximately 200–145 million years ago), as evidenced by diverse freshwater pulmonate assemblages from the in , USA, including genera such as Gyraulus and Planorbis-like forms exhibiting characteristic sinistral coiling. By the , Planorbidae had achieved a near-global distribution in freshwater environments, reflecting early adaptations to lentic habitats. Diversification accelerated during the , with a major radiation in the period, where species richness increased notably in the , coinciding with expanding continental freshwater systems. This trend continued into the following the Cretaceous-Paleogene , during which Planorbidae demonstrated resilience, with assemblages persisting across the boundary in North American and Mexican deposits, adapting to post-extinction freshwater niches amid the recovery of aquatic ecosystems. evidence from this era includes early representatives like Proplanorbis, a genus known from strata and characterized by planispiral, sinistrally coiled shells typical of the family. The family endured subsequent extinction events with minimal losses, surviving the end-Cretaceous mass extinction and experiencing only localized impacts from minor perturbations, though diversity peaked in the with over 500 recorded in long-lived European lake systems like Lake Pannon. Pleistocene glaciations influenced regional distributions, causing and contractions that promoted in refugia, as seen in phylogeographic patterns of surviving lineages. Modern subfamilies, such as Planorbinae, trace their origins to the late , with approximately 250 extant indicating relative stability since the Eocene.

Phylogenetic relationships

Planorbidae is situated within the Hygrophila clade of the , a major lineage of gastropod mollusks characterized by air-breathing pulmonates. Molecular phylogenomic analyses using nuclear protein-coding genes place Planorbidae as part of Panpulmonata, with Hygrophila including sister families such as (pond snails) and Physidae (bladder snails); these relationships are supported by high bootstrap values in concatenated datasets from multiple taxa. Within Hygrophila, Planorbidae shares a common ancestor with dating to the Triassic-Jurassic boundary around 200 million years ago, aligning with early fossil records of pulmonate diversification. Internally, Planorbidae comprises approximately 40 genera organized into monophyletic groups, with a basal split often delineating subfamilies such as Bulininae (including Bulinus) and Planorbinae (including Biomphalaria and Gyraulus). Cladistic analyses reveal multiple independent origins of limpet-like forms, particularly in Ancylinae and related lineages, where shell morphology has converged despite phylogenetic distance; for instance, genera like Burnupia and Protancylus fall outside traditional Ancylini, rendering Ancylidae paraphyletic. The subfamily Miratestinae exhibits Gondwanan origins, likely arising in during the and dispersing to the Indo-Australian Archipelago via jump dispersal events tied to tectonic dynamics of the . Molecular evidence from markers like 18S rRNA, 28S rRNA, COI mtDNA, and complete mitogenomes confirms these relationships, with concatenated datasets of up to 2837 base pairs supporting deep divergences; for example, Bulinus represents an ancient basal lineage sister to other planorbid genera. Studies indicate trans-Atlantic dispersals, such as the American origin of Biomphalaria followed by introduction to 1.1–5 million years ago, evidenced by low genetic divergence in African species from Neotropical ancestors. Key evolutionary events include the independent evolution of sinistral coiling in Planorbidae relative to other Hygrophila, and the conservation of simultaneous hermaphroditism inherited from ancestral pulmonates, facilitating self-fertilization in isolated freshwater habitats.

Taxonomy and classification

Subfamilies and genera

The family Planorbidae, established by Rafinesque in , belongs to the superfamily Planorboidea within the clade Hygrophila (formerly Basommatophora) of the subclass . Current taxonomy recognizes three subfamilies: Ancylinae Rafinesque, ; Miratestinae P. Sarasin & F. Sarasin, 1897; and Planorbinae Rafinesque, , with Planorbinae being the largest and most diverse, encompassing cosmopolitan taxa characterized by discoidal, planispiral shells. The subfamily Ancylinae includes limpet-like freshwater snails adapted to clinging to substrates, while Miratestinae is primarily represented in with more varied shell forms. Planorbinae is further divided into tribes such as Planorbini, Helisomatini, and Drepanotrematini, reflecting monophyletic groupings supported by molecular phylogenies. The family comprises approximately 40 genera and around 250 species, with recent molecular studies confirming the monophyly of key lineages and leading to mergers or revisions of some genera, such as the integration of certain taxa previously considered distinct. Notable genera include Planorbis Müller, 1774, primarily distributed in Europe with tightly coiled shells; Helisoma Swainson, 1840, native to North America and featuring wider, more orb-like whorls; Biomphalaria Preston, 1910, with about 40 species mainly in tropical Africa and the Americas; Gyraulus Charpentier, 1837, encompassing around 200 globally distributed species in shallow freshwater habitats; and Anisus Smith, 1881, common in temperate regions with sinistral coiling. These genera exemplify the family's morphological diversity, from tightly coiled planorbids to more flattened forms.

Diversity and notable species

The family Planorbidae comprises approximately 250 species across about 40 genera, making it one of the more diverse groups of freshwater pulmonate gastropods. is particularly high in tropical and subtropical regions, where environmental conditions support a wide array of habitats from rivers to temporary pools. Many Planorbidae exhibit micro-endemism, with populations restricted to isolated wetlands or ancient lakes that foster unique evolutionary divergences. Notable species include Biomphalaria glabrata, a Neotropical snail native to and a key intermediate host for the parasite , which causes intestinal . In , Planorbarius corneus, the great ramshorn snail, is a common inhabitant of standing and slow-moving waters, often reaching densities that influence algal communities. North America's Helisoma anceps occupies a broad range in ponds, lakes, and streams, with demonstrated potential for introduction and establishment beyond its native range through human-mediated dispersal. The European limpet snail Ancylus fluviatilis clings to substrates in flowing waters across much of the continent, exemplifying the family's adaptation to lotic environments. The genus Gyraulus stands out for its exceptional diversity, with around 200 described worldwide, though molecular studies suggest many additional undescribed taxa persist in understudied regions. Conservation concerns are limited, as most Planorbidae are categorized as Least Concern by the IUCN, but habitat degradation from and threatens localized populations, including several Gyraulus assessed as Vulnerable. Several Planorbidae have been introduced globally via aquarium trade and water transport, expanding their ranges beyond native distributions; for instance, Indoplanorbis exustus has established populations across and , where it competes with indigenous snails.

Human significance

Role in aquaculture and as pets

Planorbidae snails, commonly known as ramshorn snails, are widely utilized in the aquarium trade due to their hardiness and ability to consume , uneaten food, and decaying plant matter, thereby aiding in tank maintenance. Species such as are particularly popular, available in various colors including red, brown, and translucent forms selectively bred for ornamental appeal, and they thrive in a range of freshwater aquarium conditions without requiring specialized heating or filtration beyond standard setups. In aquaculture, certain Planorbidae species serve as a reliable food source for larval and . For instance, Helisoma anceps is cultured to provide live prey for species like the , with optimal growth and reproduction occurring at temperatures of 16–20°C and low levels (0–5 mg/L total nitrogen), allowing for controlled production in rearing systems. These snails also help manage populations in ornamental ponds and aquaculture facilities, contributing to by grazing on biofilms without harming or plants when densities are regulated. Cultivation of Planorbidae for aquarium pets, fish food, bait, or research is straightforward, requiring only aerated freshwater, aquatic plants for grazing, and supplemental feeding with blanched vegetables or fish flakes; they can be mass-reared in small tanks as hermaphrodites that lay clusters of 10–40 eggs hatching in 2–5 weeks. Their ease of breeding facilitates hobbyist propagation but necessitates monitoring to prevent unchecked reproduction. A primary challenge in maintaining Planorbidae in aquariums is , which can lead to resource competition and aesthetic clutter; populations are controlled by limiting food availability or using baited traps with to remove excess individuals. Additionally, escapes from hobbyist tanks have resulted in unintended introductions, with like Planorbella trivolvis establishing populations worldwide through aquarium trade releases, including in European waters.

Medical and ecological importance

Planorbidae snails, particularly species in the genus Biomphalaria, serve as intermediate hosts for the trematode parasite , which causes intestinal (also known as bilharzia) in humans. These snails facilitate the parasite's life cycle by releasing cercariae into freshwater, where they penetrate human skin during contact, leading to infection primarily in tropical and subtropical regions of and the . Globally, schistosomiasis required preventive treatment for an estimated 251.4 million people in 2021, with S. mansoni transmitted via Planorbidae contributing significantly to this burden, especially in endemic areas where poor exacerbates transmission. Certain Planorbidae species also act as first intermediate hosts for the trematode Ribeiroia ondatrae, which causes severe limb malformations in such as frogs and salamanders. The parasite's metacercariae encyst in developing amphibian limbs, disrupting and leading to extra limbs, missing digits, or other deformities that reduce survival rates and contribute to population declines in affected ecosystems. This role highlights Planorbidae's involvement in wildlife health threats beyond human disease. Control efforts targeting Planorbidae as vectors include chemical molluscicides like , which selectively kill snails while minimizing environmental harm when applied judiciously. Biological controls, such as introducing predator fish (e.g., African catfish in ), have shown promise in reducing snail densities and interrupting transmission. The (WHO) supports integrated strategies combining these with mass drug administration of , as part of the 2021–2030 roadmap for , which aims to achieve elimination of as a problem in 69 endemic countries by 2025. Ecologically, Planorbidae species function as bioindicators of freshwater quality, with their abundance and community structure reflecting levels, heavy metal contamination, and overall due to their sensitivity to environmental stressors. As grazers on , diatoms, and , they contribute to nutrient recycling by breaking down and facilitating the transfer of nutrients through food webs in aquatic habitats. However, in eutrophic systems enriched by nutrient runoff, Planorbidae can proliferate excessively, leading to overgrazing of and that disrupts and alters microbial communities. Invasive Planorbidae, such as Indoplanorbis exustus, disrupt native ecosystems by rapidly colonizing new regions through high fecundity and self-fertilization, outcompeting local snail species and altering dynamics in tropical freshwater bodies. Similarly, introduced Biomphalaria species like B. glabrata have established populations outside their native Neotropics, creating novel transmission foci for S. mansoni and threatening in invaded African and Asian wetlands. These invasions exacerbate ecological imbalances by modifying habitat structure and facilitating parasite spillover to non-native hosts.

References

  1. https://www.molluscabase.org/aphia.php?p=taxdetails&id=153908
  2. https://www.sciencedirect.com/science/article/pii/B9780123850287000111
  3. https://pmc.ncbi.nlm.nih.gov/articles/PMC10719988/
  4. https://www.mdfrc.org.au/bugguide/display.asp?type=5&class=21&subclass=&Order=57&family=217&couplet=0
  5. https://www.sciencedirect.com/science/article/pii/B9780126906479500119
  6. https://www.sciencedirect.com/science/article/pii/B9780128225219000411
  7. https://www.biodiversitylibrary.org/page/6519705
  8. https://edis.ifas.ufl.edu/publication/IN1234
  9. https://animaldiversity.org/accounts/Planorbidae/
  10. https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/planorbidae
  11. https://www.molluscs.at/gastropoda/freshwater/planorbidae.html
  12. http://www.ap.smu.ca/~lcampbel/NorthAmericanFreshwaterSnails_walkerana_vol2_no61_80.pdf
  13. https://pmc.ncbi.nlm.nih.gov/articles/PMC1567689/
  14. https://prepare4vbd.eu/wp-content/uploads/2022/12/FG_Introduction_1998_Eng.pdf
  15. https://digitalcommons.iwu.edu/cgi/viewcontent.cgi?article=1851&context=jwprc
  16. https://www.researchgate.net/publication/354265400_Growth_and_Reproduction_of_Planorbarius_corneus_Linnaeus_1758_in_Laboratory_Conditions
  17. https://www.frontiersin.org/journals/medicine/articles/10.3389/fmed.2021.614797/full
  18. https://www.jstor.org/stable/26789686
  19. https://link.springer.com/article/10.1007/s10750-014-2130-z
  20. https://www.researchgate.net/publication/240589279_Influence_of_temperature_on_survival_and_growth_of_two_freshwater_planorbid_species_Planorbarius_corneus_L_and_Planorbis_planorbis_L
  21. https://www.foliamalacologica.com/Distribution-of-the-freshwater-snail-Gyraulus-rossmaessleri-Auerswald-1852-Mollusca%2C190413%2C0%2C2.html
  22. https://www.foliamalacologica.com/pdf-143378-70206?filename=Food%2520preferences%2520of%2520the.pdf
  23. https://www.sciencedirect.com/science/article/abs/pii/S0163104781924110
  24. https://setac.onlinelibrary.wiley.com/doi/10.1002/etc.5686
  25. https://www.researchgate.net/publication/233617180_Resource_use_and_partitioning_by_two_co-occurring_freshwater_gastropod_species
  26. https://www.researchgate.net/publication/225806204_Winning_the_biodiversity_arms_race_among_freshwater_gastropods_Competition_and_coexistence_through_shell_variability_and_predator_avoidance
  27. https://pmc.ncbi.nlm.nih.gov/articles/PMC7046736/
  28. https://www.zoologyverse.com/classification-of-planorbis
  29. https://onlinelibrary.wiley.com/doi/10.1111/brv.13016
  30. https://pubs.usgs.gov/pp/0233b/report.pdf
  31. https://bioone.org/journals/paleontological-research/volume-14/issue-4/1342-8144-14.4.233/Terrestrial-and-Freshwater-Pulmonate-Gastropods-from-the-Early-Cretaceous-Kuwajima/10.2517/1342-8144-14.4.233.full
  32. https://www.sciencedirect.com/science/article/abs/pii/S0195667123002008
  33. https://www.molluscabase.org/aphia.php?p=taxdetails&id=1420635
  34. https://bmcecolevol.biomedcentral.com/articles/10.1186/s12862-018-1273-3
  35. https://parasitesandvectors.biomedcentral.com/articles/10.1186/1756-3305-3-57
  36. https://www.sciencedirect.com/science/article/abs/pii/S1055790313002765
  37. https://pmc.ncbi.nlm.nih.gov/articles/PMC2914737/
  38. https://www.sciencedirect.com/science/article/abs/pii/S1055790302002804
  39. https://onlinelibrary.wiley.com/doi/10.1111/j.1463-6409.2006.00258.x
  40. https://www.sciencedirect.com/science/article/abs/pii/S1055790320302761
  41. https://pmc.ncbi.nlm.nih.gov/articles/PMC10889216/
  42. https://pmc.ncbi.nlm.nih.gov/articles/PMC10598177/
  43. https://doi.org/10.3390/ijms25042279
  44. https://www.mdpi.com/1422-0067/25/4/2279
  45. https://www.tandfonline.com/doi/full/10.1080/13235818.2025.2469203
  46. https://pmc.ncbi.nlm.nih.gov/articles/PMC8158356/
  47. https://pmc.ncbi.nlm.nih.gov/articles/PMC11623786/
  48. https://explorer.natureserve.org/Taxon/ELEMENT_GLOBAL.2.108947/Helisoma_anceps
  49. https://www.sciencedirect.com/science/article/pii/S1439609206000390
  50. https://pmc.ncbi.nlm.nih.gov/articles/PMC4985174/
  51. https://downloads.regulations.gov/FWS-R4-ES-2022-0070-0035/attachment_2.pdf
  52. https://keys.lucidcentral.org/keys/v3/freshwater_molluscs/key/australian_freshwater_molluscs/Media/Html/entities/planorbarius_corneus.htm
  53. https://onlinelibrary.wiley.com/doi/abs/10.1111/are.13556
  54. https://downloads.regulations.gov/FWS-R4-ES-2022-0070-0035/attachment_3.pdf
  55. https://www.researchgate.net/publication/372583018_Invasion_potential_of_the_aquarium_pet_snail_Planorbella_trivolvis_in_India_impact_of_certain_abiotic_and_biotic_factors
  56. https://www.fwgna.org/species/planorbidae/h_scalaris_duryi.html
  57. https://pubmed.ncbi.nlm.nih.gov/11719572/
  58. https://www.frontiersin.org/journals/tropical-diseases/articles/10.3389/fitd.2023.1143186/full
  59. https://www.who.int/news-room/fact-sheets/detail/schistosomiasis
  60. https://onlinelibrary.wiley.com/doi/10.1111/j.1461-0248.2004.00610.x
  61. https://pmc.ncbi.nlm.nih.gov/articles/PMC11315061/
  62. https://idpjournal.biomedcentral.com/articles/10.1186/s40249-016-0153-6
  63. https://journals.plos.org/plosntds/article?id=10.1371/journal.pntd.0013490
  64. https://www.who.int/publications/i/item/9789240010352
  65. https://pmc.ncbi.nlm.nih.gov/articles/PMC8647957/
  66. https://www.molluscs.at/gastropoda/freshwater2.html
  67. https://www.mdpi.com/2073-4441/13/2/235
  68. https://www.cambridge.org/core/product/identifier/S0022149X00703658/type/journal_article
  69. https://www.researchgate.net/publication/7610011_Biological_invasions_The_case_of_planorbid_snails
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