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]
Marisa cornuarietis is a native Brazilian species which is often kept in aquariums in other countries worldwide.
Pomacea commissionis (Ihering, 1898)
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)
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
Biomphalaria glabrata is a medically important species, because it is a host for the parasite Schistosoma mansoni .
Anisancylus dutrae (Santos, 1994) – synonym: Gundlachia dutrae [ 15]
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)
This section
needs expansion . You can help by
adding to it .
(September 2009 )
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]
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
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)
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]
Veronicellidae
Belocaulus angustipes (Heynemann, 1885)
Belocaulus willibaldoi Ohlweiler, Mota & Gomes, 2009
Phyllocaulis renschi Thomé, 1965
Phyllocaulis boraceiensis Thomé, 1976[ 5]
Phyllocaulis soleiformis (d'Orbigny, 1835)
Phyllocaulis tuberculosus (Martens, 1868)
Phyllocaulis variegatus (Semper, 1885)
Sarasinula dubia (Semper, 1885)
Sarasinula linguaeformis (Semper, 1885)
Sarasinula marginata (Semper, 1885)
Sarasinula plebeia (Fischer, 1868)
Vaginulus taunayi Férussac, 1821[ 5]
This section
needs expansion . You can help by
adding to it .
(September 2009 )
This section
needs expansion . You can help by
adding to it .
(September 2009 )
This section
needs expansion . You can help by
adding to it .
(September 2009 )
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
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)
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]
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)
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]
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)
Bivalvia
116 species.
This section
needs expansion . You can help by
adding to it .
(September 2009 )
See also
Lists of molluscs of surrounding countries:
References
^ 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 Naturkunde A 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
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