List of non-marine molluscs of Brazil

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

Location 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(?) 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]

Summary table of number of species
Brazil
freshwater gastropods about 250
land gastropods about 700 (590 species of snails and 110(?) species of slugs)
gastropods altogether over 950
bivalves at least 117
molluscs altogether 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 altogether 32

In Rio 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]

In Santa 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

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

Ampullariidae[1]

Marisa cornuarietis is a native Brazilian species which is often kept in aquariums in other countries worldwide.

Pleuroceridae

  • Doryssa schuppi (Ihering, 1902)

Cochliopidae

  • Atomicus inopinatus Simone & Rolán, 2021[9]
  • Heleobia apua Simone & Rolán, 2021[9]
  • Heleobia australis (d’Orbigny, 1835)
  • Heleobia bertoniana Pilsbry, 1911
  • Heleobia charruana d’Orbigny, 1843
  • Heleobia cuzcoensis (Pilsbry, 1911)
  • Heleobia davisi (Silva & Thomé, 1985)
  • Heleobia nana Marcus & Marcus, 1963
  • Heleobia parchappei (d’Orbigny, 1835)
  • Heleobia piscium (d’Orbigny, 1835) – synonyms: Littoridina (= Heleobia) piscium (= australis) (d’Orbigny, 1835)
  • Heleobia pukua Simone & Rolán, 2021[9]
  • Heleobia robusta Silva & Veitenheimer-Mendes, 2004

Tateidae

  • Potamolithus catharinae Pilsbry, 1911
  • Potamolithus jacuhyensis Pilsbry, 1899
  • Potamolithus phillippianus Pilsbry, 1911
  • Potamolithus ribeirensis Pilsbry, 1911
  • Potamolithus troglobius[10]

Pomatiopsidae

Thiaridae

Planorbidae

Biomphalaria glabrata is a medically important species, because it is a host for the parasite Schistosoma mansoni.

Chilinidae

  • Chilina fluminea (d’Orbigny, 1835)
  • Chilina globosa Frauenfeld, 1881
  • Chilina parva Martens, 1868
  • Chilina rushii Pilsbry, 1896

Physidae

  • Aplexa marmorata (Guilding, 1828) – Aplexa (Stenophysa) marmorata
  • Aplexa rivalis (Maton & Rackett, 1807)[14]
  • Physa acuta Draparnaud, 1805 – synonym: Physa cubensis

Lymnaeidae

Land gastropods

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)

  • Alcadia iheringi Wagner, 1910
  • 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)

  • Neocyclotus agassizi (Bartsch & Morrison, 1942)
  • Neocyclotus amazonense (Bartsch & Morrison, 1942)
  • Neocyclotus blanchetianus (Moricand, 1836)
  • Neocyclotus brasiliensis (Gray, 1839)
  • Neocyclotus currani (Bartsch & Morrison, 1942)
  • Neocyclotus fultoni (Bartsch & Morrison, 1942)
  • Neocyclotus hedui (Bartsch & Morrison, 1942)
  • Neocyclotus inca (d’Orbigny, 1835)
  • Neocyclotus incomptus (Sowerby, 1850)
  • Neocyclotus merrilli (Bartsch & Morrison, 1942)
  • Neocyclotus moricandi (Pfeiffer, 1852)
  • Neocyclotus prominulus (d’Orbigny, 1835)
  • Neocyclotus redfieldi (Bartsch & Morrison, 1942)
  • Neocyclotus stramineus (Reeve, 1843)

Diplommatinidae (complete)

  • Adelopoma brasiliense
  • Adelopoma paraguayana Parodiz, 1944[5]

Vertiginidae (complete)

  • Gastrocopta iheringi (Suter, 1900)
  • Gastrocopta oblonga
  • Gastrocopta servilis – subspecies Gastrocopta servilis oblonga (Pfeiffer, 1853)[4]
  • Gastrocopta solitaria

Pyramidulidae

  • Pyramidula compacta Suter, 1900[4]

Valloniidae (complete)

  • Vallonia pulchella
  • Pupisoma dioscoricola (Adams, 1845)
  • Pupisoma minus Pilsbry, 1920[4]
  • Strobilops brasiliana

Succineidae (complete)

  • Succinea burmeisteri Döring[4]
  • Succinea lopesi Lanzieri, 1966
  • Succinea manaosensis Pilsbry, 1926
  • Succinea meridionalis d’Orbigny, 1837
  • Succinea pusilla Pfeiffer, 1849
  • Succinea repanda Pfeiffer, 1854
  • Oxyloma beckeri Lanzieri, 1966
  • Omalonyx brasiliensis (Simroth, 1896)
  • Omalonyx convexa (Martens, 1868)
  • Omalonyx unguis (d’Orbigny, 1837)

Ellobiidae

Achatinidae

Charopidae (complete)

  • Radiodiscus bolachaensis Fonseca & Thomé, 1995
  • Radiodiscus cuprinus Fonseca & Thomé, 2000[4]
  • Radiodiscus iheringi (Ancey, 1899)
  • Radiodiscus patagonicus (Suter, 1900)
  • Radiodiscus promatensis Miquel, Ramírez & Thomé, 2004[4]
  • Radiodiscus thomei Weyrauch, 1965
  • Radiodiscus vazi Fonseca & Thomé, 1995
  • Radioconus amoenus (Thiele, 1927)
  • Radioconus costellifer Hylton-Scott, 1957
  • Radioconus goeldii (Thiele, 1927)
  • Ptychodon amancaezensis (Hidalgo, 1869)
  • Ptychodon liciae (Vaz, 1991)
  • Ptychodon janeirensis (Thiele, 1927)
  • Ptychodon schuppi (Suter, 1900)
  • Rydleya quinquelirata (Smith, 1890)
  • Trochogyra gordurasensis (Thiele, 1927)
  • Trochogyra leptotera Rochebrune & Mabille, 1882[15]
  • Trochogyra pleurophora (Moricand, 1846)
  • Trochogyra superba (Thiele, 1927)
  • Zilchogyra zulmae Miquel, Ramírez & Thomé, 2004[4]

Helicodiscidae (complete)

  • Zilchogyra clara (Thiele, 1927)
  • Zilchogyra deliciosa (Thiele, 1927)
  • Zilchogyra paulistana (Hylton-Scott, 1973)
  • Lilloiconcha gordurasensis (Thiele, 1927)
  • Lilloiconcha tucumana (Hylton-Scott, 1963)
  • Helicodiscus thereza Thiele, 1927

Punctidae (complete)

Zonitidae (complete)

Veronicellidae

Milacidae

Limacidae

Agriolimacidae

Philomycidae

Euconulidae (complete)

  • Habroconus angueinus (Ancey, 1892) – synonym: Habroconus angüinus (Ancey, 1892)
  • Habroconus goyazensis (Ancey, 1901)
  • Habroconus martinezi (Hidalgo, 1869)
  • Habroconus mayi (Baker, 1914)
  • Habroconus semenline Moricand, 1846 – synonym: Habroconus (Pseudoguppya) semenlini (Moricand, 1845)
  • Euconulus fulvus (Müller, 1774)[4]
  • Guppya sp.[4]

Ferussaciidae (complete)

  • Cecilioides blandiana (Crosse, 1880)
  • Cecilioides consobrina (d’Orbigny, 1841)
  • Cecilioides gundlachi (Pfeiffer, 1850)

Discidae

  • Discus alternatus (Say, 1816)[4]

Subulinidae (complete)

Subulina octona
  • Subulina octona (Bruguière, 1789)
  • Subulina parana Pilsbry, 1906
  • Leptinaria bequaerti Pilsbry, 1926
  • Leptinaria charlottei Baker, 1923
  • Leptinaria concentrica (Reeve, 1849)
  • Leptinaria lamellata (Potiez & Michaud, 1838)
  • Leptinaria mamoreensis Baker, 1926
  • Leptinaria monodon (C. B. Adams, 1849)[5]
  • Leptinaria parana Pilsbry, 1926
  • Leptinaria ritchiei Pilsbry, 1907
  • Leptinaria unilamellata (d’Orbigny, 1835)[5]
  • Lamellaxis gracilis (Hutton, 1834)
  • Lamellaxis micra (d’Orbigny, 1835) – synonym: Allopeas micra (d’Orbigny, 1835)
  • Opeas beckianum (Pfeiffer, 1846)
  • Opeas goodalli (Miller, 1822)
  • Opeas octogyrum (Pfeiffer, 1856)
  • Opeas opella Pilsbry & Vanatta, 1906
  • Rumina decollata (Linnaeus, 1758)
  • Synapterpes coronatus (Pfeiffer, 1846)
  • Synapterpes hanleyi (Pfeiffer, 1846)
  • Obeliscus agassizi Pilsbry, 1906[2]
  • Obeliscus carphodes (Pfeiffer, 1852)[2]
  • Obeliscus columella (Philippi, 1844)[2]
  • Obeliscus obeliscus (Moricand, 1833)[2]
  • Obeliscus pattalus Pilsbry, 1906[2]
  • Obeliscus planospirus (Pfeiffer, 1852)[2]
  • Obeliscus sylvaticus (Spix, 1827)[2]
  • Obeliscus subuliformis (Moricand, 1836)[2]
  • Neobeliscus calcareus (Born, 1778)[2]
  • Vegrandinia trindadensis (Breure and Coelho, 1976) – synonym: Bulimulus trindadensis Breure & Coelho, 1976

Megaspiridae (complete)

  • Callionepion iheringi Pilsbry & Vanatta, 1899
  • Megaspira elata (Gould, 1847)
  • Megaspira elatior (Spix, 1827)
  • Megaspira iheringi Pilsbry, 1926
  • Megaspira ruschenbergiana Jay, 1836

Oleacinidae (complete)

Strophocheilidae (complete)

  • Anthinus albolabiatus (Jaeckel, 1927)
  • 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 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 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)

  • Peltella iheringi Leme, 1968
  • 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)
The shell of Corona perversa.
  • 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 turbinatus, synonym Tomigerus turbinatus, that was endemic to Brazil, is now extinct.

Bulimulidae

  • 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 Simone, 2012 – genus endelic to Brazil, with 3 species[17]
  • Oxychona bifasciata (Burrow, 1815)
  • Oxychona blanchetiana (Moricand, 1833)
  • Oxychona lonchostoma (Menke, 1828)
  • 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)

Scolodontidae (complete)

  • Scolodonta amazonica (Dohrn, 1882)[2]
  • Scolodonta bounoboena (d’Orbigny, 1835)[2]
  • Scolodonta interrupta (Suter, 1900)[2]
  • Scolodonta mutata (Gould, 1846)[2]
  • Scolodonta nitidula (Dohrn, 1882)[2]
  • Scolodonta spirorbis (Deshayes, 1850)[2]
  • Systrophia eatoni Baker, 1914
  • Systrophia siolii Haas, 1955
  • Entodina cheilostropha (d’Orbigny, 1835)
  • Entodina derbyi (Ihering, 1912)
  • Entodina exigua (Thiele, 1927)
  • Entodina jekylli Baker, 1914
  • Entodina lundi (Mörch, 1871)
  • Drepanostomella sp.[4]
  • Wayampia sp.[4]
  • Happia ammoniformis (d’Orbigny, 1835)
  • Happia ammonoceras (Pfeiffer, 1854)
  • Happia besckei (Dunker, 1847)
  • Happia euspira (Pfeiffer, 1854)
  • Happia grata Thiele, 1927
  • Happia iheringi (Clessin, 1888)
  • Happia insularis (Böttger, 1889)
  • Happia microdiscus Thiele, 1927
  • Happia mülleri Thiele, 1927
  • Happia pilsbryi Lange-de-Morretes, 1949
  • Happia snethlagei Baker, 1914
  • Happia vitrina (Wagner, 1827)
  • Miradiscops brasiliensis (Thiele, 1927)
  • Tamayops banghaasi (Thiele, 1927)

Streptaxidae (complete)

  • Huttonella bicolor (Hutton, 1834) – First report in 2008.[18]
  • Martinella prisca Thiele, 1927[2]
  • Rectartemon apertus (Martens, 1868)[2]
  • Rectartemon candidus (Spix, 1827)[2]
  • Rectartemon cappilosus (Pilsbry, 1897)[2]
  • Rectartemon cryptodon (Moricand, 1851)[2]
  • Rectartemon depressus (Heynemann, 1868)[4]
  • Rectartemon helios (Pilsbry, 1897)[2]
  • Rectartemon hylephilus (d’Orbigny, 1835)[2]
  • Rectartemon intermedius (Albers, 1857)[2]
  • Rectartemon mulleri (Thiele, 1927)[2]
  • Rectartemon politus (Fulton, 1899)[2]
  • Rectartemon rollandi (Bernardi, 1857)[2]
  • Rectartemon spixianus (Pfeiffer,1841)[2]
  • Rectartemon wagneri (Pfeiffer, 1841)[2]
  • Hypselartemon alveus (Dunker, 1845)[2][19]
  • Hypselartemon contusulus (Férussac, 1827)[19]
  • Hypselartemon deshayesianus (Crosse, 1863)[2][19]
  • Hypselartemon paivanus (Pfeiffer, 1867)[2][19]
  • Streptaxis contusus (Férussac, 1821)[2]
  • Streptaxis decussatus Pilsbry, 1897[2]
  • Streptaxis dunkeri Pfeiffer, 1845[2]
  • Streptaxis iguapensis Pilsbry, 1930[2]
  • Streptaxis iheringi Thiele, 1827[2]
  • Streptaxis lutzelburgi Weber, 1925[2]
  • Streptaxis pfeifferi (Pilsbry, 1930)[2]
  • Streptaxis piquetensis (Pilsbry, 1930)[2]
  • Streptaxis regius Lobbecke, 1881[2]
  • Streptaxis saopaulensis Pilsbry, 1930[2]
  • Streptaxis subregularis Pfeiffer, 1846[2]
  • Streptaxis tumulus Pilsbry, 1897[2]
  • Streptaxis uberiformis Pfeiffer, 1848[2]
  • Streptartemon abunaensis (Baker, 1914)[2]
  • Streptartemon candeanus (Petit, 1842)[2]
  • Streptartemon comboides (d’Orbigny, 1835)[2]
  • Streptartemon cookeanus (Baker, 1914)[2]
  • Streptartemon crossei (Pfeiffer, 1867)[2]
  • Streptartemon cumingianus (Pfeiffer, 1849)[2]
  • Streptartemon decipiens (Crosse, 1865)[2]
  • Streptartemon deformis (Férussac, 1821)[2]
  • Streptartemon dejectus (Petit, 1842)[2]
  • Streptartemon deplanchei (Drouet, 1859)[2]
  • Streptartemon elata (Moricand, 1846)[2]
  • Streptartemon extraneus Haas, 1955[2]
  • Streptartemon glaber (Pfeiffer, 1849)[2]
  • Streptartemon quixadensis (Baker, 1914)[2]
  • Streptartemon streptodon (Moricand, 1851)[2]
  • Sairostoma perplexum Haas, 1938[2]

Camaenidae (complete)

  • Polygyratia polygyrata (Born, 1778)

Pleurodontidae (complete)

  • Labyrinthus furcillatus (Hupé, 1853)
  • Labyrinthus raimondii (Philippi, 1867)
  • Labyrinthus yatesi (Pfeiffer, 1855)
  • Solaropsis amazonica (Pfeiffer, 1854)
  • Solaropsis anguicula (Hupé, 1853)
  • Solaropsis bachi Ihering, 1900
  • Solaropsis brasiliana (Deshayes, 1831)
  • Solaropsis cearana (Baker, 1914)
  • Solaropsis cicatricata Beck, 1837
  • Solaropsis derbyi (Ihering, 1900)
  • Solaropsis elaps Dohrn, 1882
  • Solaropsis fairchildi Bequaert & Clench, 1938
  • Solaropsis feisthameli (Hupé, 1853)
  • Solaropsis heliaca (d’Orbigny, 1835)
  • Solaropsis johnsoni Pilsbry, 1933
  • Solaropsis leopoldina (Strubel, 1895)
  • Solaropsis pascalia (Cailliaud, 1857)
  • Solaropsis pilsbryi Ihering, 1900
  • Solaropsis rosarium (Pfeiffer, 1849)
  • Solaropsis rugifera Dohrn, 1882
  • Solaropsis serpens (Spix, 1827)
  • Solaropsis trigonostoma Haas, 1934
  • Solaropsis undata (Lightfoot, 1786)
  • Solaropsis vipera (Pfeiffer, 1859)

Bradybaenidae (complete)

Epiphragmophoridae (complete)

  • Epiphragmophora bernardius
  • Epiphragmophora semiclausa (Martens, 1868)

Helicidae (complete)

Bivalvia

116 species.

See also

Lists of molluscs of surrounding countries:

References
  1. 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)
  2. 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.
  3. (in Portuguese) (2009) PORTARIA No 125, DE 07 DE AGOSTO DE 2009, accessed 7 April 2010.
  4. 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.
  5. 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.
  6. 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.
  7. 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.
  8. 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
  9. Simone, L.R.L.; Rolán, E. (2021). "A new genus and three new species of freshwater cochliopids (Caenogastropoda) from Goiás, Brazil". Iberus. 31 (1).
  10. 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.
  11. Malek E. A. (1983). "The South American hydrobioid genus Idiopyrgus Pilsbry, 1911". The Nautilus 97(1): 16-20.
  12. 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.
  13. 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.
  14. 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
  15. 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.
  16. 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.
  17. 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 Naturkunde A 9: 1–7. doi:10.18476/sbna.v9.a1.
  18. 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.
  19. 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
  • Haas F. 1959. Inland mollusks from Venezuela, southern Brazil, and Peru. Fieldiana: Zoology, 39(31): 363–371.
  • L. R. L. Simone (2006) Land and Freshwater Molluscs of Brazil. 390 pp.
  • Agudo-Padrón A. I. (2009) "New malacological records from Paraná State, Southern Brazil region, with a general synthesys of current knowledge". Ellipsaria 11(1): 11–13.
  • Agudo-Padrón A. I. (2009) "New malacological records from Paraná State, Southern Brazil Region. II. Supplementary Annex". Ellipsaria 11(2): 6–7.
  • Agudo-Padrón A. I. (2009) "Endangered continental mollusks of Santa Catarina State, Southern Brazil: An Overview". Ellipsaria 11(2): 7–8.
  • Agudo-Padrón A. I. (2009) "General mollusk fauna of Rio Grande do Sul State, Southernmost Brazil Region: a Preliminary Revision Rehearsal. II. New Bibliographical Records". Ellipsaria 11(2): 9–10.
  • Agudo-Padrón A. I. (2011). "Mollusca and environmental conservation in Santa Catarina State (SC, Southern Brazil): current situation". Biodiversity Journal 2: 3–8. PDF.
  • Agudo-Padrón A. I. (2011). "Current knowledge on population studies on five continental molluscs (Mollusca, Gastropoda et Bivalvia) of Santa Catarina State (SC, Central Southern Brazil region)". Biodiversity Journal 2: 9–12. PDF.
  • Agudo-Padrón A. I. (2011). "Exotic molluscs in Santa Catarina’s State, Southern Brazil region (Mollusca, Gastropoda et Bivalvia): check list and regional spatial distribution knowledge". Biodiversity Journal 2: 53–58. PDF.
  • Agudo-Padrón A. I. (2011). "Threatened freshwater and terrestrial molluscs of Santa Catarina State, Southern Brazil (Mollusca, Gastropoda et Bivalvia): check list and evaluation of regional threats". Biodiversity Journal 2: 59–66. PDF.
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