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Contents

   



(Top)
  


1 Freshwater gastropods  


1.1  Ampullariidae[1]  




1.2  Pleuroceridae  




1.3  Cochliopidae  




1.4  Tateidae  




1.5  Pomatiopsidae  




1.6  Thiaridae  




1.7  Planorbidae  




1.8  Chilinidae  




1.9  Physidae  




1.10  Lymnaeidae  






2 Land gastropods  


2.1  Helicinidae (complete)  




2.2  Neocyclotidae (complete)  




2.3  Diplommatinidae (complete)  




2.4  Vertiginidae (complete)  




2.5  Pyramidulidae  




2.6  Valloniidae (complete)  




2.7  Succineidae (complete)  




2.8  Ellobiidae  




2.9  Achatinidae  




2.10  Charopidae (complete)  




2.11  Helicodiscidae (complete)  




2.12  Punctidae (complete)  




2.13  Zonitidae (complete)  




2.14  Milacidae  




2.15  Limacidae  




2.16  Agriolimacidae  




2.17  Philomycidae  




2.18  Euconulidae (complete)  




2.19  Ferussaciidae (complete)  




2.20  Discidae  




2.21  Subulinidae (complete)  




2.22  Megaspiridae (complete)  




2.23  Oleacinidae (complete)  




2.24  Strophocheilidae (complete)  




2.25  Orthalicidae (complete include subfamilies according to the Bouchet & Rocroi, 2005)  




2.26  Simpulopsidae  




2.27  Odontostomidae  




2.28  Bulimulidae  




2.29  Scolodontidae (complete)  




2.30  Streptaxidae (complete)  




2.31  Camaenidae (complete)  




2.32  Pleurodontidae (complete)  




2.33  Bradybaenidae (complete)  




2.34  Epiphragmophoridae (complete)  




2.35  Helicidae (complete)  






3 Bivalvia  




4 See also  




5 References  




6 Further reading  




7 External links  













List of non-marine molluscs of Brazil







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From Wikipedia, the free encyclopedia
  

Location of Brazil

The non-marine molluscs of Brazil are a part of the molluscan fauna of Brazil.

There are at least 1,074[1] native nominal species of non-marine molluscs living in Brazil.

There are at least 956[1] nominal species of gastropods, which breaks down to about 250 species of freshwater gastropods, and about 700[1] species of land gastropods (590 species of snails[2] and approximately 110(?)[citation needed] species of slugs), plus at least 117[1] species of bivalves living in the wild.

There are at least 373 species of freshwater molluscs in Brazil.[1]

The number of native species is at least 1,074[1] and the number of non-indigenous molluscs in Brazil is, at minimum, 32 species.[1] The most serious invasive alien species in Paraná State are the land snail Achatina fulica and the freshwater snail Melanoides tuberculata.[3]

Numbers of species in Brazil
Freshwater gastropods About 250
Land gastropods: snails 590
Land gastropods: slugs 110(?)
Gastropods (total) over 950
Bivalves at least 117
Molluscs (total) 1107
Non-indigenous gastropods in the wild ? freshwater and ? land
Non-indigenous synantrop gastropods ?
Non-indigenous bivalves in the wild ?
Non-indigenous synantrop bivalves ?
Non-indigenous molluscs (total) 32

InRio Grande do Sul, 201 species and subspecies of non-marine mollusks were recorded: 156 gastropods (83 land snails + 18 slugs + 55 freshwater snails) and 45 bivalves.[4]

InSanta Catarina, 158 species and subspecies of non-marine mollusk were recorded: 135 gastropods (103 land gastropods + 32 freshwater snails) and 23 bivalves.[5]

Freshwater gastropods[edit]

The following list of freshwater gastropods is based on the two southernmost states.[4][5]

Ampullariidae[1][edit]

Marisa cornuarietis is a native Brazilian species which is often kept in aquariums in other countries worldwide.
  • Asolene petiti (Crosse, 1891)[6]
  • Asolene platae (Maton, 1809)
  • Asolene spixii (d'Orbigny, 1838)
  • Pomacea aldersoni (Pain, 1946)[1]
  • Pomacea armeniacum Hupé, 1857
  • Pomacea aulanieri (Hupé & Deville, 1850)
  • Pomacea amazonica Reeve, 1856
  • Pomacea archimedis Spix, 1827
  • Pomacea aurostoma (Lea, 1856)
  • Pomacea avellana (Sowerby, 1909)
  • Pomacea baeri (Dautzenberg, 1902)
  • Pomacea bridgesii (Reeve, 1856)
  • Pomacea camena Pain, 1949
  • Pomacea canaliculata (Lamarck, 1804)
  • Pomacea castelnaudii Hupé, 1957[1]
  • Pomacea catamarcensis (Sowerby, 1875)
  • Pomacea columellaris Gould, 1848
  • Pomacea consolatrix (Ihering, 1919)
  • Pomacea cousini (Jousseaume, 1887)
  • Pomacea curumim Simone, 2004
  • Pomacea decussata (Moricand, 1836)
  • Pomacea dolioides (Reeve, 1856)
  • Pomacea eximia (Dunker, 1853)
  • Pomacea expansa (Miller, 1879)
  • Pomacea falconensis Pain & Arias, 1958
  • Pomacea gevesensis (Deshayes, 1838)
  • Pomacea glauca (Linnaeus, 1758)
  • Pomacea hanleyana (Alderson, 1926)
  • Pomacea haustrum (Reeve, 1856)[7]
  • Pomacea hollingsworthi (Pain, 1946)
  • Pomacea insularum (d'Orbigny, 1835)[7]
  • Pomacea interrupta (Sowerby, 1909)
  • Pomacea levior Sowerby, 1909
  • Pomacea lineata (Spix, 1827)[8]
  • Pomacea maculata Perry, 1810
  • Pomacea martinezi (Hidalgo, 1866)
  • Pomacea megastoma (Sowerby, 1825)
  • Pomacea meta Ihering, 1915
  • Pomacea minuscula Baker, 1930
  • Pomacea modesta (Busch, 1859)
  • Pomacea nais Pain, 1949
  • Pomacea nigrilabris Philippi, 1851
  • Pomacea nobilis Reeve, 1856
  • Pomacea nubila Reeve, 1856
  • Pomacea oblonga (Swainson, 1823)
  • Pomacea palmeri (Marshall, 1930)
  • Pomacea paludosa (Say, 1829)
  • Pomacea papyracea Spix, 1827
  • Pomacea pealiana (Lea, 1838)
  • Pomacea pernambucensis Reeve, 1856
  • Pomacea physoides Reeve, 1856
  • Pomacea planorbula Philippi, 1851
  • Pomacea prunella Hupé, 1857
  • Pomacea pulchra Gray, 1834
  • Pomacea pomatia (Martens, 1857)
  • Pomacea producta Reeve, 1856
  • Pomacea puntaplaya (Cousin, 1887)
  • Pomacea quersina Spix, 1827
  • Pomacea quinindensis (Miller, 1879)
  • Pomacea reyrei (Cousin, 1887)
  • Pomacea scalaris Orbigny, 1835
  • Pomacea semitecta (Mousson, 1873)
  • Pomacea semperi (Kobelt, 1914)
  • Pomacea sordida Swainson, 1823
  • Pomacea superba (Marshall, 1926)
  • Pomacea urceus (Müller, 1774)
  • Pomacea swainsoni (Philippi, 1852)
  • Pomacea tenuissima (Jousseaume, 1894)
  • Pomacea vexillum (Reeve, 1856)
  • Pomacea yatesii Reeve, 1856
  • Pomacea zischkai Blume & Pain, 1952
  • Pomacea zonata Spix, 1827
  • Pomella americanista (Ihering, 1919)
  • Felipponea elongata (Dall, 1921)
  • Felipponea iheringi (Pilsbry, 1933)
  • Felipponea neritiformis Dall, 1919
  • Marisa cornuarietis (Linnaeus, 1758)

    • Pleuroceridae[edit]

    Cochliopidae[edit]

    Tateidae[edit]

    Pomatiopsidae[edit]

    Thiaridae[edit]

    Planorbidae[edit]

    Biomphalaria glabrata is a medically important species, because it is a host for the parasite Schistosoma mansoni.
  • Anisancylus obliquus (Broderip & Sowerby, 1832)
  • Burnupia ingae Lanzer, 1991
  • Ferrissia gentilis Lanzer, 1991
  • Gundlachia ticaga (Marcus & Marcus, 1962)
  • Hebetancylus moricandi (d'Orbigny, 1837) – synonym: Gundlachia moricandi
  • Laevapex vazi Santos, 1989[1]
  • Uncancylus concentricus (d'Orbigny, 1835) – synonym: Gundlachia concentrica
  • Antillorbis nordestensis (Lucena, 1954)
  • Biomphalaria cousini[16]
  • Biomphalaria glabrata (Say, 1818)
  • Biomphalaria occidentalis Paraense, 1981
  • Biomphalaria oligoza Paraense, 1975
  • Biomphalaria peregrina (d'Orbigny, 1835)
  • Biomphalaria schrammi (Crosse, 1864)
  • Biomphalaria tenagophila (d'Orbigny, 1835)
    • Subspecies:
    • B. t. tenagophila (d'Orbigny, 1835)
    • B. t. guaibensis (Paraense, 1984)
  • Biomphalaria straminea (Dunker, 1848)
  • Acrorbis petricola Odhner, 1937
  • Drepanotrema anatinum (d'Orbigny, 1935)
  • Drepanotrema cimex (Moricand, 1839)
  • Drepanotrema depressissimus (Moricand, 1839)
  • Drepanotrema heloicum (d'Orbigny, 1835)
  • Drepanotrema kermatoides (d'Orbigny, 1835)
  • Drepanotrema lucidum (Pfeiffer, 1839)
  • Drepanotrema pfeifferi (Strobel, 1874)

    • Chilinidae[edit]

    Physidae[edit]

    Lymnaeidae[edit]

    Land gastropods[edit]

    The listing of land snails is complete for snails based on Saldago (2003).[2] The slug listings are probably incomplete because they are based on list from two southernmost states only.[4][5]

    Helicinidae (complete)[edit]

  • Alcadia paraensis (Pfeiffer, 1859)
  • Helicina angulata Sowerby, 1842
  • Helicina angulifera Wagner, 1910
  • Helicina besckei Pfeiffer, 1848
  • Helicina bicincta Gloyne, 1872
  • Helicina brasiliensis Gray, 1824
  • Helicina caracolla Moricand, 1836
  • Helicina carinata d'Orbigny, 1835
  • Helicina concentrica Pfeiffer, 1848
  • Helicina densestriata Wagner, 1910 – synonym: Oxyrhombus densestriatus Wagner, 1910
  • Helicina fulva d'Orbigny, 1835
  • Helicina guajarana Baker, 1914
  • Helicina haematostoma Moricand, 1839
  • Helicina iguapensis Pilsbry, 1900
  • Helicina inaequistriata Pilsbry, 1900
  • Helicina juruana Ihering, 1904
  • Helicina laterculus Baker, 1914
  • Helicina leopoldinae Wagner, 1906
  • Helicina leptrotopis Wagner, 1910
  • Helicina leucozonalis Ancey, 1892
  • Helicina lirifera Ancey, 1892
  • Helicina lundi Beck, 1858
  • Helicina menkeana Philippi, 1847
  • Helicina moreletiana Pfeiffer, 1851
  • Helicina oxytropis Gray, 1839
  • Helicina schereri Baker, 1914
  • Helicina siolii Haas, 1949
  • Helicina sordida King & Broderip, 1832
  • Helicina tilei Pfeiffer, 1847
  • Helicina variabilis Wagner, 1827
  • Helicina wettsteini Wagner, 1906
  • Proserpina derbyi Dall, 1905

    • Neocyclotidae (complete)[edit]

    Diplommatinidae (complete)[edit]

    Vertiginidae (complete)[edit]

    Pyramidulidae[edit]

    Valloniidae (complete)[edit]

    Succineidae (complete)[edit]

    Ellobiidae[edit]

    Achatinidae[edit]

    Charopidae (complete)[edit]

    Helicodiscidae (complete)[edit]

    Punctidae (complete)[edit]

    Zonitidae (complete)[edit]

    Veronicellidae

    Milacidae[edit]

    Limacidae[edit]

    Agriolimacidae[edit]

    Philomycidae[edit]

    Euconulidae (complete)[edit]

    Ferussaciidae (complete)[edit]

    Discidae[edit]

    Subulinidae (complete)[edit]

    Subulina octona

    Megaspiridae (complete)[edit]

    Oleacinidae (complete)[edit]

    Strophocheilidae (complete)[edit]

  • Anthinus henselii (Martens, 1868)
  • Anthinus miersi (Sowerby, 1838)
  • Anthinus multicolor (Rang, 1831)
  • Anthinus turnix (Gould, 1846)
  • Gonyostomus goniostomus (Férussac, 1821)
  • Gonyostomus egregius (Pfeiffer, 1845)
  • Gonyostomus insularis Leme, 1974
  • Mirinaba antoninensis (Lange-de-Morretes, 1952)
  • Mirinaba cadeadensis (Lange-de-Morretes, 1952)
  • Mirinaba curytibana (Lange-de-Morretes, 1952)
  • Mirinaba cuspidens (Lange-de-Morretes, 1952)
  • Mirinaba erythrosoma (Pilsbry, 1895)
  • Mirinaba fusoides (Bequaert, 1948)
  • Mirinaba jaussaudi (Lange-de-Morretes, 1937)
  • Mirinaba planidens (Michelin, 1831)
  • Mirinaba unidentata (Sowerby, 1825)
  • Speironepion iguapensis (Pilsbry, 1901)
  • Speironepion kronei (Ihering, 1901)
  • Speironepion milleri (Sowerby, 1838)
  • Speironepion pilsbryi (Ihering, 1900)
  • Strophocheilus calus Pilsbry, 1901
  • Strophocheilus contortuplicatus (Reeve, 1850)
  • Strophocheilus debilis Bequaert, 1948
  • Strophocheilus miersi Da Costa, 1904
  • Strophocheilus pudicus (Müller, 1774)
  • Strophocheilus roseolabris Bequaert, 1948
  • Megalobulimus abbreviatus (Bequaert, 1948)
  • Megalobulimus albescens (Bequaert, 1948)
  • Megalobulimus albus (Bland & Binney, 1872)
  • Megalobulimus amandus Simone, 2012[22]
  • Megalobulimus arapotiensis Lange-de-Morretes, 1952
  • Megalobulimus auritus (Sowerby, 1838)
  • Megalobulimus bereniceae (Lange-de-Morretes, 1952)
  • Megalobulimus bertae Lange-de-Morretes, 1952
  • Megalobulimus bronni (Pfeiffer, 1847)
  • Megalobulimus capillaceus (Pfeiffer, 1855)
  • Megalobulimus cardosoi (Lange-de-Morretes, 1952)
  • Megalobulimus chionostoma (Mörch, 1852)
  • Megalobulimus conicus (Bequaert, 1948)
  • Megalobulimus dryades Fontenelle, Simone & Cavallari 2021[23]
  • Megalobulimus elongatus (Bequaert, 1948)
  • Megalobulimus foreli (Bequaert, 1948)
  • Megalobulimus fragilior (Ihering, 1901)
  • Megalobulimus garbeanus (Leme, 1964)
  • Megalobulimus globosus (Martens, 1876)
  • Megalobulimus grandis (Martens, 1885)
  • Megalobulimus granulosus (Rang, 1831)
  • Megalobulimus gummatus (Hidalgo, 1870)
  • Megalobulimus haemastomus (Scopoli, 1786)
  • Megalobulimus hector (Pfeiffer, 1857)
  • Megalobulimus intertextus (Pilsbry, 1895)
  • Megalobulimus klappenbachi (Leme, 1964)
  • Megalobulimus leonardosi (Lange-de-Morretes, 1952)
  • Megalobulimus lopesi Leme, 1989
  • Megalobulimus maximus (Sowerby, 1825)
  • Megalobulimus mogianensis Simone & Leme, 1998
  • Megalobulimus musculus (Bequaert, 1948)
  • Megalobulimus nodai Lange-de-Morretes, 1952
  • Megalobulimus oblongus (Müller, 1774)
  • Megalobulimus oliveirai (Bequaert, 1948)
  • Megalobulimus oosomus (Pilsbry, 1895)
  • Megalobulimus ovatus (Müller, 1774)
  • Megalobulimus parafragilior Leme & Indrusiak, 1990
  • Megalobulimus paranaguensis (Pilsbry & Ihering, 1900)
  • Megalobulimus pergranulatus (Pilsbry, 1901)
  • Megalobulimus pintoi Lange-de-Morretes, 1952
  • Megalobulimus popelairianus (Nyst, 1845)
  • Megalobulimus proclivis (Martens, 1888)
  • Megalobulimus pygmaeus (Bequaert, 1948)
  • Megalobulimus riopretensis Simone & Leme, 1998
  • Megalobulimus rolandianus Lange-de-Morretes, 1952
  • Megalobulimus sanctipauli (Ihering & Pilsbry, 1900)
  • Megalobulimus terrestris (Spix, 1827)
  • Megalobulimus torii Lange-de-Morretes, 1937
  • Megalobulimus valenciennesii (Pfeiffer, 1842)
  • Megalobulimus vestitus (Pilsbry, 1926)
  • Megalobulimus wohlersi Lange-de-Morretes, 1952
  • Megalobulimus yporanganus (Ihering & Pilsbry, 1901)

    • Orthalicidae (complete include subfamilies according to the Bouchet & Rocroi, 2005)[edit]

    The shell of Corona perversa.
    Biotocus turbinatus, synonym Tomigerus turbinatus, that was endemic to Brazil, is now extinct.
  • Peltella palliolum (Férussac, 1821)
  • Plekocheilus floccosus (Spix, 1827)
  • Plekocheilus pentadinus (d'Orbigny, 1835)
  • Plekocheilus piperitus (Sowerby, 1838)
  • Plekocheilus pseudopiperatus (Moricand, 1858)
  • Plekocheilus rhodocheilus (Reeve, 1848)
  • Eudolichotis distorta (Bruguière, 1789)
  • Eudolichotis lacerta (Pfeiffer, 1855)
  • Auris bernardii (Pfeiffer, 1856)
  • Auris bilabiata (Broderip & Sowerby, 1829)
  • Auris brachyplax Pilsbry, 1896
  • Auris chrysostoma (Moricand, 1836)
  • Auris egregia (Jay, 1836)
  • Auris illheocola (Moricand, 1836)
  • Auris melanostoma (Moricand, 1836)
  • Auris melastoma (Swainson, 1820)
  • Auris nigrilabris Pilsbry, 1896
  • Thaumastus achilles (Pfeiffer, 1852)
  • Thaumastus ascendens (Pfeiffer, 1852)
  • Thaumastus baixoguanduensis Pena, Coelho & Salgado, 1996
  • Thaumastus hebes Strebel, 1910
  • Thaumastus largillierti (Philippi, 1845)
  • Thaumastus magnificus (Grateloup, 1839)
  • Thaumastus nehringi (Martens, 1889)
  • Thaumastus requieni (Pfeiffer, 1852)
  • Thaumastus spixii (Wagner, 1827)
  • Thaumastus taunasii (Férussac, 1822)
  • Thaumastus tiradentensis Pena, Coelho & Salgado, 1996
  • Lopesianus cremulatus Weyrauch, 1958
  • Aposcutalus atlanticus (Dutra & Leme, 1985)
  • Otostomus signatus (Spix, 1827)
  • Cochlorina aurisleporis (Bruguière, 1792)
  • Cochlorina aurismuris (Moricand, 1839)
  • Cochlorina involuta (Martens, 1867)
  • Cochlorina lateralis (Menke, 1828)
  • Cochlorina navicula (Wagner, 1827)
  • Cochlorina uranops (Pilsbry, 1898)
  • Pseudoxychona dulcis (Ihering, 1912)
  • Pseudoxychona pileiformis (Moricand, 1836)
  • Pseudoxychona polytricha (Ihering, 1912)
  • Pseudoxychona spiritualis (Ihering, 1912)
  • Rhinus ciliatus (Gould, 1846)
  • Rhinus durus (Spix, 1827)
  • Rhinus evelinae Leme, 1989
  • Rhinus heterograma (Moricand, 1836)
  • Rhinus heterotrichus (Moricand, 1836)
  • Rhinus koseritzi (Clessin, 1888)
  • Rhinus longisetus (Moricand, 1846)
  • Rhinus obeliscus (Haas, 1936)
  • Rhinus ovulum (Reeve, 1849)
  • Rhinus pubescens (Moricand, 1846)
  • Rhinus rochai (Baker, 1914)
  • Rhinus scobinatus (Wood, 1828)
  • Rhinus suturalis (Baker, 1914)
  • Rhinus taipuensis (Baker, 1914)
  • Rhinus thomei (Weyrauch, 1967)
  • Rhinus velutinohispidus (Moricand, 1836)
  • Simpulopsis atrovirens (Moricand, 1836)
  • Simpulopsis brasiliensis (Moricand, 1846)
  • Simpulopsis corrugata Guppy, 1866
  • Simpulopsis decussata Pfeiffer, 1856
  • Simpulopsis gomesae Silva & Thomé, 2006[4]
  • Simpulopsis miersi Pfeiffer, 1856
  • Simpulopsis ovata (Sowerby, 1822)
  • Simpulopsis promatensis Silva & Thomé 2006[4]
  • Simpulopsis pseudosulculosa Breure, 1975
  • Simpulopsis rufovirens (Moricand, 1846)
  • Simpulopsis sulculosa (Férussac, 1821)
  • Simpulopsis tryoni Pilsbry, 1899
  • Simpulopsis wiebesi Breure, 1975
  • Eudioptus araujoi (Breure, 1975)
  • Eudioptus boissieri (Moricand, 1846)
  • Eudioptus citrinovitreus (Moricand, 1836)
  • Eudioptus luteolus (Ancey, 1901)
  • Eudioptus progastor (d'Orbigny, 1835)
  • Eudioptus pseudosuccineus (Moricand, 1836)
  • Sultana meobambensis (Pfeiffer, 1855)
  • Sultana sultana (Dillwyn, 1817)
  • Corona duckei Ihering, 1915
  • Corona incisa (Hupé, 1857)
  • Corona loroisiana (Hupé, 1857)
  • Corona machadoensis Strebel, 1909
  • Corona perversa (Swaison, 1821)
  • Corona regalis (Hupé, 1857)
  • Corona regina (Férussac, 1823)
  • Corona ribeiroi Ihering, 1915
  • Orthalicus bensoni (Reeve, 1849)
  • Orthalicus capax (Pilsbry, 1930)
  • Orthalicus mars Pfeiffer, 1861
  • Orthalicus phlogerus (d'Orbigny, 1835)
  • Orthalicus prototypus (Pilsbry, 1899)
  • Orthalicus pulchellus (Spix, 1827)
  • Orthalicus varius Martens, 1873
  • Orthalicus zonatus Strebel, 1909
  • Hyperaulax ramagei (Smith, 1890)
  • Hyperaulax ridleyi (Smith, 1890)
  • Anctus angiostomus (Wagner, 1827)
  • Anctus laminiferus (Ancey, 1888)
  • Cyclodontina branneri (Dall, 1909)
  • Cyclodontina ciarana (Dohrn, 1882)
  • Cyclodontina costulata (Ancey, 1904)
  • Cyclodontina exesa (Spix, 1827)
  • Cyclodontina fidaensis (Moricand, 1858)
  • Cyclodontina fusiformis (Menke, 1828)
  • Cyclodontina guarani (d'Orbigny, 1835)
  • Cyclodontina iheringi (Marshall, 1926)
  • Cyclodontina inflata (Wagner, 1827)
  • Cyclodontina labrosa (Menke, 1828)
  • Cyclodontina longula (Pfeiffer, 1859)
  • Cyclodontina punctatissima (Lesson, 1830)
  • Cyclodontina rhodinostoma (d'Orbigny, 1835)
  • Cyclodontina salobrensis Solem, 1956
  • Cyclodontina scrabella (Dohrn, 1882)
  • Cyclodontina squarrosus (Ancey, 1904)
  • Cyclodontina tudiculata (Martens, 1868)
  • Bahiensis albofilosus (Dohrn, 1883)
  • Bahiensis bahiensis (Moricand, 1833)
  • Bahiensis janeirensis (Sowerby, 1838)
  • Bahiensis miliolus (d'Orbigny, 1835)
  • Bahiensis occultus (Reeve, 1849)
  • Bahiensis reevei (Deshayes, 1851)
  • Bahiensis ringens (Dunker, 1847)
  • Moricandia angulata (Wagner, 1827)
  • Moricandia auriscervina (Férussac, 1821)
  • Moricandia bouvieri (Dautzenberg, 1896)
  • Moricandia dubiosa (Jay, 1839)
  • Moricandia nasuta (Martens, 1886)
  • Moricandia toleratus (Fulton, 1903)
  • Moricandia willi (Dohrn, 1883)
  • Spixia hilairii (Pfeiffer, 1845)
  • Spixia paraguayana (Ancey, 1892)
  • Spixia striata (Spix, 1827)
  • Plagiodontes trayrae (Jaeckel, 1950)
  • Clessinia costata (Pfeiffer, 1848)
  • Clessinia neglecta (Pfeiffer, 1847)
  • Clessinia oblita (Reeve, 1848)
  • Odontostomus dautzenbergianus Pilsbry, 1898
  • Odontostomus degeneratus Pilsbry, 1899
  • Odontostomus fasciatus (Pfeiffer, 1869)
  • Odontostomus gargantuus (Rang, 1831)
  • Odontostomus gemellatus Ancey, 1901
  • Odontostomus grayanus (Pfeiffer, 1845)
  • Odontostomus königswaldi (Thiele, 1906)
  • Odontostomus leucotremus (Beck, 1837)
  • Odontostomus odontostomus (Sowerby, 1824)
  • Odontostomus paulistus Pilsbry & Ihering, 1898
  • Odontostomus sexdentatus (Spix, 1827)
  • Odontostomus simplex (Thiele, 1906)
  • Odontostomus squarrosus Ancey, 1904
  • Odontostomus thielei (Pilsbry, 1930)
  • Tomigerus clausus Spix, 1827
  • Tomigerus corrugatus Ihering, 1905
  • Tomigerus esamianus Salgado & Coelho, 1990
  • Tomigerus laevis Ihering, 1905
  • Tomigerus matthewsi Salgado & Leme, 1991
  • Tomigerus pilsbryi Baker, 1914
  • Tomigerus rochai Ihering, 1905
  • Digerus gibberulus (Burrow, 1815), synonym: Tomigerus gibberulus – extinct
  • Biotocus cumingi (Pfeiffer, 1849)
  • Biotocus turbinatus (Pfeiffer, 1845), synonym: Tomigerus turbinatus – extinct
  • Biotocus ubajarensis (Leme, 1980)
  • Anostoma baileyi Solem, 1956
  • Anostoma depressum Lamarck, 1822
  • Anostoma deshayesianum Fischer, 1857
  • Anostoma octodentatum Fischer von Waldheim, 1807
  • Anostoma rossi Weber, 1925
  • Ringicella carinatum (Pfeiffer, 1853)
  • Ringicella luetzelburgi (Weber, 1925)
  • Ringicella ringens (Linnaeus, 1758)

    • Simpulopsidae[edit]

    Odontostomidae[edit]

    Bulimulidae[edit]

  • Bulimulus angustus Weyrauch, 1966
  • Bulimulus brunoi (Ihering, 1917)
  • Bulimulus corumbaensis Pilsbry, 1897
  • Bulimulus dukinfieldi Melvill, 1900
  • Bulimulus eganus (Pfeiffer, 1853)
  • Bulimulus ephippium Ancey, 1904
  • Bulimulus erectus (Reeve, 1849)
  • Bulimulus marcidus (Pfeiffer, 1852)
  • Bulimulus sporadicus (d'Orbigny, 1835)
  • Bulimulus stilbe Pilsbry, 1901
  • Bulimulus tenuissimus (Férussac, 1832)
  • Bulimulus vesicalis (Pfeiffer, 1853)
  • Naesiotus arnaldoi (Lanzieri & Rezende, 1971)
  • Naesiotus carlucioi (Rezende & Lanzieri, 1963)
  • Naesiotus cutisculptus Ancey, 1901
  • Naesiotus eudioptus "Ihering", Pilsbry, 1897
  • Naesiotus lopesi (Rezende, Lanzieri & Inada, 1972)
  • Naesiotus montivagus (d'Orbigny, 1835)
  • Naesiotus pachys (Pilsbry, 1897)
  • Kora corallina Simone, 2012 (endemic)[26]
  • Kora nigra Simone, 2015[27] (endemic)
  • Kora rupestris Salvador & Simone, 2016[28] (endemic)
  • Oxychona bifasciata (Burrow, 1815)
  • Oxychona blanchetiana (Moricand, 1833)
  • Oxychona lonchostoma (Menke, 1828)
  • Oxychona maculata Salvador & Cavallari, 2013[29]
  • Oxychona pyramidella (Wagner, 1827)
  • Drymaeus acervatus (Pfeiffer, 1857)
  • Drymaeus acuminatus Da Costa, 1906
  • Drymaeus balteatus Pilsbry, 1898
  • Drymaeus bivittatus (Sowerby, 1833)
  • Drymaeus branneri Baker, 1914
  • Drymaeus bucia (Pfeiffer, 1859)
  • Drymaeus coarctatus (Pfeiffer, 1845)
  • Drymaeus cuticulus (Pfeiffer, 1855)
  • Drymaeus dutaillyi (Pfeiffer, 1856)
  • Drymaeus edmülleri (Albers, 1854)
  • Drymaeus expansus (Pfeiffer, 1848)
  • Drymaeus flexilabris (Pfeiffer, 1853)
  • Drymaeus gereti Ancey. 1901
  • Drymaeus germaini (Ancey, 1892)
  • Drymaeus hygrohylaeus (d'Orbigny, 1835)
  • Drymaeus interpunctus (Martens, 1887)
  • Drymaeus limicolarioides Haas, 1936
  • Drymaeus lusorius (Pfeiffer, 1848)
  • Drymaeus lynchi Parodiz, 1946
  • Drymaeus magus (Wagner, 1827)
  • Drymaeus muelleggeri Jaeckel, 1927
  • Drymaeus nigrogularis (Dohrn, 1882)
  • Drymaeus oreades (d'Orbigny, 1835)
  • Drymaeus papyraceus (Mawe, 1823)
  • Drymaeus papyrifactus Pilsbry, 1898
  • Drymaeus poecilus (d'Orbigny, 1835)
  • Drymaeus protractus (Pfeiffer, 1855)
  • Drymaeus ribeiroi Ihering, 1915
  • Drymaeus roseatus (Reeve, 1848)
  • Drymaeus saccatus (Pfeiffer, 1855)
  • Drymaeus semistriatus Haas, 1955
  • Drymaeus similaris (Moricand, 1856)
  • Drymaeus siolii Haas, 1952
  • Drymaeus souzalopesi Weyrauch, 1965
  • Drymaeus subsimilaris Pilsbry, 1898
  • Drymaeus succineus Pilsbry, 1901
  • Drymaeus suprapunctatus Baker, 1914
  • Drymaeus vanattai Pilsbry, 1898
  • Leiostracus cinnamomeolineatus (Moricand, 1841)
  • Leiostracus clouei (Pfeiffer, 1856)
  • Leiostracus goniotropis (Ancey, 1904)
  • Leiostracus manoeli (Moricand, 1841)
  • Leiostracus melanoscolops (Dohrn, 1882)
  • Leiostracus obliquus (Reeve, 1849)
  • Leiostracus onager (Beck, 1837)
  • Leiostracus perlucidus (Spix, 1827)
  • Leiostracus sarchochilus (Pfeiffer, 1837)
  • Leiostracus subtuszonatus (Pilsbry, 1899)
  • Leiostracus vimineus (Moricand, 1833)
  • Leiostracus vittatus (Spix, 1827)
  • Spixia coltrorum Simone, 2012[22]

    • Scolodontidae (complete)[edit]

    Streptaxidae (complete)[edit]

    Camaenidae (complete)[edit]

    Pleurodontidae (complete)[edit]

    Bradybaenidae (complete)[edit]

    Epiphragmophoridae (complete)[edit]

    Helicidae (complete)[edit]

    Bivalvia[edit]

    116 species.

    See also[edit]

    Lists of molluscs of surrounding countries:

    References[edit]

    1. ^ a b c d e f g h i j k Simone, L. R. L. 2006. Land and Freshwater Molluscs of Brazil. EGB, Fapesp. São Paulo, Brazil. 390 pp. ISBN 85-906670-0-6. (book review Archived 28 September 2011 at the Wayback Machine)[page needed]
  • ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj Salgado, Norma Campos; Coelho, Arnaldo C. dos Santos (2003). "Moluscos terrestres do Brasil (Gastrópodes operculados ou não, exclusive Veronicellidae, Milacidae e Limacidae)" [Terrestrial molluscs of Brazil (Gastropoda, operculate or not, exclusive Veronicellidae, Milacidae and Limacidae)]. Revista de Biología Tropical (in Portuguese). 51 (3): 149–89.
  • ^ (in Portuguese) (2009) PORTARIA No 125, DE 07 DE AGOSTO DE 2009, accessed 7 April 2010.
  • ^ a b c d e f g h i j k l m n o p q r s t u v w x Agudo-Padrón A. I. (14 May) 2009. Recent Terrestrial and Freshwater Molluscs of Rio Grande do Sul State, RS, Southern Brazil Region: A Comprehensive Synthesis and Check List Archived 5 November 2012 at the Wayback Machine. Visaya April 2009, pages 1–13.
  • ^ a b c d e f g h i j k Aisur Ignacio Agudo-Padrón (21 July) 2008. Recent Terrestrial And Freshwater Molluscs Of Santa Catarina State, Sc, Southern Brazil Region: A Comprehensive Synthesis And Check List. Visaya April 2009, pages 1–12.
  • ^ Pastorino G. & Darrigan G. (2011). "Asolene petiti". In: IUCN 2012. IUCN Red List of Threatened Species. Version 2012.2. <www.iucnredlist.org>. Downloaded on 7 February 2013.
  • ^ a b Rawlings TA, Hayes KA, Cowie RH, Collins TM (2007). "The identity, distribution, and impacts of non-native apple snails in the continental United States". BMC Evolutionary Biology. 7: 97. doi:10.1186/1471-2148-7-97. PMC 1919357. PMID 17594487.
  • ^ Alves R. R. N. 2009. Fauna used in popular medicine in Northeast Brazil. Journal of Ethnobiology and Ethnomedicine 2009, 5:1. doi:10.1186/1746-4269-5-1
  • ^ a b c Simone, L.R.L.; Rolán, E. (2021). "A new genus and three new species of freshwater cochliopids (Caenogastropoda) from Goiás, Brazil". Iberus. 31 (1).
  • ^ Simone, L.R.L.; Oliveira, G.V.d. (2021). "A new species of the micro snail genus Heleobia (Caenogastropoda, Cochliopidae) from Bahia, Brazil". Papéis Avulsos de Zoologia. 61: e20216143.
  • ^ a b c Simone, Luiz Ricardo L. (25 March 2021). "Freshwater micro-gastropods from the Iguaçu National Park, Brazil: two new truncatelloid caenogastropods and anatomy of Chilina megastoma Hylton Scott, 1958". Folia Malacologica. 29 (1): 13–32. doi:10.12657/folmal.029.002.
  • ^ Bichuette, Maria Elina; Trajano, Eleonora (September 2003). "A population study of epigean and subterranean Potamolithus snails from southeast Brazil (Mollusca: Gastropoda: Hydrobiidae)". Hydrobiologia. 505 (1–3): 107–17. doi:10.1023/B:HYDR.0000007299.26220.b8. S2CID 35607414. INIST 15383655.
  • ^ Malek E. A. (1983). "The South American hydrobioid genus Idiopyrgus Pilsbry, 1911". The Nautilus 97(1): 16-20.
  • ^ Simone, L. R. L. (2012). "A new genus and species of cavernicolous Pomatiopsidae (Mollusca, Caenogastropoda) in Bahia, Brazil" (PDF). Papéis Avulsos de Zoologia. 52 (40): 515–524. doi:10.1590/s0031-10492012022000001.
  • ^ dos Santos; S. B. (2003). "Estado atual do conhecimento dos ancilídeos na América do Sul (Mollusca: Gastropoda: Pulmonata: Basommatophora)" (PDF). Revista de Biología Tropical (in Portuguese). 51 (3): 191–223. Retrieved 1 June 2014.
  • ^ Teodoro T. M., Janotti-Passos L. K., Carvalho O. d. S. & Caldeira R. L. (2010). "Occurrence of Biomphalaria cousini (Mollusca: Gastropoda) in Brazil and its susceptibility to Schistosoma mansoni (Platyhelminths: Trematoda)". Molecular Phylogenetics and Evolution 57(1): 144–151. doi:10.1016/j.ympev.2010.05.019.
  • ^ Martins R. T. & Alves R. da G. 2008. Occurrence of Naididae (Annelida: Oligochaeta) from three gastropod species in irrigation fields in southeastern Brazil. Biota Neotropica, 8(3), doi:10.1590/S1676-06032008000300023
  • ^ a b c Simone, L. R. L. (2013). "Habeas, a new genus of Diplommatinidae from central Bahia, Brazil (Caenogastropoda), with description of three new species". Journal of Conchology. 41 (4): 519–525.
  • ^ Mansur, M.C.D. 1996. Trochogyra leptotera. In: IUCN 2009. IUCN Red List of Threatened Species. Version 2009.2. <www.iucnredlist.org>. Downloaded on 20 November 2009.
  • ^ a b Teixeira CG, Thiengo SC, Thome JW, Medeiros AB, Camillo-Coura L, Agostini AA (1993). "On the diversity of mollusc intermediate hosts of Angiostrongylus costaricensis Morera & Cespedes, 1971 in southern Brazil". Memórias do Instituto Oswaldo Cruz. 88 (3): 487–9. doi:10.1590/S0074-02761993000300020. PMID 8107609.
  • ^ Jardim, J. A.; Abbate, D.; Simone, L. R. L. (2013). "A new species of Euglandina (Pulmonata, Spiraxidae) from Brazil". Journal of Conchology. 41 (3): 327–330.
  • ^ a b c Simone, L. R. L. (2012). "Taxonomical study on a sample of pulmonates from Santa Maria da Vitória, Bahia, Brazil, with description of a new genus and four new species (Mollusca: Orthalicidae and Megalobulimidae)". Papéis Avulsos de Zoologia. 52 (36): 431–439. doi:10.1590/S0031-10492012021600001.
  • ^ Fontenelle, J.H.; Simone, L.R.L.; Cavallari, D.C. (2021). "Megalobulimus dryades, a new species from the Atlantic Forest in southeastern Brazil, and redescription of Megalobulimus gummatus (Gastropoda: Strophocheilidae)". Papéis Avulsos de Zoologia. 61: e202161442/17. doi:10.11606/1807-0205/2021.61.44.
  • ^ a b c d e Simone, L. R. L.; Casati, R. (3 July 2013). "New land mollusk fauna from Serra da Capivara, Piauí, Brazil, with a new genus and five new species (Gastropoda: Orthalicoidea, Streptaxidae, Subulinidae)". Zootaxa. 3683 (2): 145–158. doi:10.11646/zootaxa.3683.2.4.
  • ^ Simone, L.R.L. (2018). "The presence of the Argentinian genus Pilsbrylia in Brazil, with description of a new species (Gastropoda, Odontostomidae)". Journal of Conchology. 43 (1): 13–16.
  • ^ Simone L. R. L. (2012). "Taxonomical study on a sample of pulmonates from Santa Maria da Vitória, Bahia, Brazil, with description of a new genus and four new species (Mollusca: Orthalicidae and Megalobulimidae)". Papéis Avulsos de Zoologia 52(36): 431–439. doi:10.1590/S0031-10492012021600001, HTML.
  • ^ Simone L. R. L. (2015). "Three new species of Kora (Pulmonata, Orthalicidae) from Bahia and Minas Gerais, Brazil". Journal of Conchology 42(1): 51–56.
  • ^ Salvador R. B. & Simone L. R. L. (2016). "A new species of Kora from Bahia, Brazil (Gastropoda: Pulmonata: Orthalicoidea), with an emended diagnosis of the genus". Stuttgarter Beiträge zur NaturkundeA 9: 1–7. doi:10.18476/sbna.v9.a1.
  • ^ Salvador, R. B.; Cavallari, D. C. (2013). "A new Oxychona species (Gastropoda: Pulmonata: Orthalicidae) from Bahia state, Brazil". Journal of Conchology. 41 (3): 315–318.
  • ^ Santos S. B. dos, Viana T. A. & Fonseca F. C. (2008). "First record of the micro-predator Huttonella bicolor (Hutton, 1834) (Gastropoda, Streptaxidae) on Rio de Janeiro city, Brazil". Biociências, Porto Alegre, 16(2): 145–148. PDF.
  • ^ a b c d Barbosa A. F., Salgado N. C. & Coelho A. C. d. S. (2008) "Taxonomy, Comparative Morphology, and Geographical Distribution of the Neotropical Genus Hypselartemon Wenz, 1947 (Gastropoda: Pulmonata: Streptaxidae)". Malacologia, 50(1–2): 1–12. doi:10.4002/0076-2997-50.1.1

    • Further reading[edit]

    External links[edit]


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