List of non-marine molluscs of Brazil

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

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 brucutu Simone & Oliveira, 2021[10]
  • Heleobia charruana d'Orbigny, 1843
  • Heleobia cuzcoensis (Pilsbry, 1911)
  • Heleobia davisi (Silva & Thomé, 1985)
  • Heleobia iguassu Simone, 2021[11]
  • 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 mirim Simone, 2021[11]
  • Potamolithus phillippianus Pilsbry, 1911
  • Potamolithus ribeirensis Pilsbry, 1911
  • Potamolithus troglobius[12]

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 megastoma Hylton Scott, 1958[11]
  • Chilina parva Martens, 1868
  • Chilina rushii Pilsbry, 1896

Physidae

  • Aplexa marmorata (Guilding, 1828) – Aplexa (Stenophysa) marmorata
  • Aplexa rivalis (Maton & Rackett, 1807)[17]
  • 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]
  • Habeas corpus Simone, 2013[18]
  • Habeas data Simone, 2013[18]
  • Habeas priscus Simone, 2013[18]

Vertiginidae (complete)

Pyramidulidae

  • Pyramidula compacta Suter, 1900[4]

Valloniidae (complete)

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[19]
  • 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

  • Milax cf. gagates (Draparnaud, 1801)[4]
  • Milax valentianus Férussac, 1821

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 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)

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

  • Rhinus gilbertus Simone & Casati, 2013[24]

Odontostomidae

  • Clinispira insolita Simone & Casati, 2013[24]
  • Anostoma tessa Simone, 2012[22]
  • Cyclodontina capivara Simone & Casati, 2013[24]
  • Pilsbrylia dalli Simone, 2018[25]

Bulimulidae

  • Anctus prolatus Simone & Casati, 2013[24]
  • 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)

  • 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.[30]
  • 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][31]
  • Hypselartemon contusulus (Férussac, 1827)[31]
  • Hypselartemon deshayesianus (Crosse, 1863)[2][31]
  • Hypselartemon paivanus (Pfeiffer, 1867)[2][31]
  • 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 molaris Simone & Casati, 2013[24]
  • 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. ^ 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]
  2. ^ 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.
  3. ^ (in Portuguese) (2009) PORTARIA No 125, DE 07 DE AGOSTO DE 2009, accessed 7 April 2010.
  4. ^ 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.
  5. ^ 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.
  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. ^ 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.
  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. ^ 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).
  10. ^ 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.
  11. ^ 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.
  12. ^ 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.
  13. ^ Malek E. A. (1983). "The South American hydrobioid genus Idiopyrgus Pilsbry, 1911". The Nautilus 97(1): 16-20.
  14. ^ 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.
  15. ^ 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.
  16. ^ 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.
  17. ^ 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
  18. ^ 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.
  19. ^ 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.
  20. ^ 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.
  21. ^ 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.
  22. ^ 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.
  23. ^ 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.
  24. ^ 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.
  25. ^ 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.
  26. ^ 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.
  27. ^ 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.
  28. ^ 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.
  29. ^ 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.
  30. ^ 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.
  31. ^ 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

  • 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.

External links

  • Conchasbrasil.org – Brazilian species of molluscs