List of non-marine molluscs 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]
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
[edit]The following list of freshwater gastropods is based on the two southernmost states.[4][5]
- 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)
- Doryssa schuppi (Ihering, 1902)
- 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
- Potamolithus catharinae Pilsbry, 1911
- Potamolithus jacuhyensis Pilsbry, 1899
- Potamolithus mirim Simone, 2021[11]
- Potamolithus phillippianus Pilsbry, 1911
- Potamolithus ribeirensis Pilsbry, 1911
- Potamolithus troglobius[12]
- Idiopyrgus souleyetianus Pilsbry, 1911[13]
- Spiripockia punctata Simone, 2012[14]
- Melanoides tuberculata (Müller, 1774)[5]
- 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)
- Chilina fluminea (d'Orbigny, 1835)
- Chilina globosa Frauenfeld, 1881
- Chilina megastoma Hylton Scott, 1958[11]
- Chilina parva Martens, 1868
- Chilina rushii Pilsbry, 1896
- Aplexa marmorata (Guilding, 1828) – Aplexa (Stenophysa) marmorata
- Aplexa rivalis (Maton & Rackett, 1807)[17]
- Physa acuta Draparnaud, 1805 – synonym: Physa cubensis
- Pseudosuccinea columella (Say, 1817)
- Lymnaea rupestris Paraense, 1982
- Lymnaea viatrix (d'Orbigny, 1835)
This section needs expansion. You can help by adding to it. (September 2009) |
Land gastropods
[edit]The listing of land snails is complete for snails based on Saldago (2003).[2] The slug listings are probably incomplete because they are based on list from two southernmost states only.[4][5]
Helicinidae (complete)
[edit]- Alcadia 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)
[edit]- 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)
[edit]- Adelopoma brasiliense
- Adelopoma paraguayana Parodiz, 1944[5]
- Habeas corpus Simone, 2013[18]
- Habeas data Simone, 2013[18]
- Habeas priscus Simone, 2013[18]
Vertiginidae (complete)
[edit]- Gastrocopta iheringi (Suter, 1900)
- Gastrocopta oblonga
- Gastrocopta servilis – subspecies Gastrocopta servilis oblonga (Pfeiffer, 1853)[4]
- Gastrocopta solitaria
- Pyramidula compacta Suter, 1900[4]
Valloniidae (complete)
[edit]- Vallonia pulchella
- Pupisoma dioscoricola (Adams, 1845)
- Pupisoma minus Pilsbry, 1920[4]
- Strobilops brasiliana
Succineidae (complete)
[edit]- 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)
- Melampus coffeus (Linnaeus, 1758)[5]
- Pedipes mirabilis (Mohlfeld, 1816)[5]
- Achatina fulica (Bowdich, 1822)[4]
Charopidae (complete)
[edit]- 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)
[edit]- 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
- Paralaoma servilis (Shuttleworth, 1852)[4]
- Punctum pilsbyi (Hylton-Scott, 1957)
- Oxychilus cellarius (Müller, 1774)
- Oxychilus nitidus (Müller, 1774)
- Oxychilus sublenticularis (Böttger, 1889)
- Zonitoides arboreus (Say, 1816)
- Zonitoides parana Baker, 1914
- 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) |
- Milax cf. gagates (Draparnaud, 1801)[4]
- Milax valentianus Férussac, 1821
This section needs expansion. You can help by adding to it. (September 2009) |
- Limax maximus Linnaeus, 1758[4][20]
- Limacus flavus[4][20]
This section needs expansion. You can help by adding to it. (September 2009) |
- Deroceras laeve (Müller, 1774)
Euconulidae (complete)
[edit]- 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)
[edit]- Cecilioides blandiana (Crosse, 1880)
- Cecilioides consobrina (d'Orbigny, 1841)
- Cecilioides gundlachi (Pfeiffer, 1850)
- Discus alternatus (Say, 1816)[4]
Subulinidae (complete)
[edit]- 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)
[edit]- Callionepion iheringi Pilsbry & Vanatta, 1899
- Megaspira elata (Gould, 1847)
- Megaspira elatior (Spix, 1827)
- Megaspira iheringi Pilsbry, 1926
- Megaspira ruschenbergiana Jay, 1836
Oleacinidae (complete)
[edit]- Euglandina irakita Jardim, Abbate & Simone, 2013[21]
- Euglandina striata
Strophocheilidae (complete)
[edit]- 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)
[edit]- 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)
- Rhinus gilbertus Simone & Casati, 2013[24]
- Clinispira insolita Simone & Casati, 2013[24]
- Anostoma tessa Simone, 2012[22]
- Cyclodontina capivara Simone & Casati, 2013[24]
- Pilsbrylia dalli Simone, 2018[25]
- 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)
[edit]- 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)
[edit]- 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)
[edit]- Polygyratia polygyrata (Born, 1778)
Pleurodontidae (complete)
[edit]- 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)
[edit]- Bradybaena similaris (Férussac, 1821)
Epiphragmophoridae (complete)
[edit]- Epiphragmophora bernardius
- Epiphragmophora semiclausa (Martens, 1868)
- Cornu aspersum (O.F. Müller, 1774)
Bivalvia
[edit]116 species.
This section needs expansion. You can help by adding to it. (September 2009) |
See also
[edit]Lists of molluscs of surrounding countries:
- List of non-marine molluscs of Venezuela
- List of non-marine molluscs of Suriname
- List of non-marine molluscs of Guyana
- List of non-marine molluscs of French Guiana
- List of non-marine molluscs of Colombia
- List of non-marine molluscs of Bolivia
- List of non-marine molluscs of Peru
- List of non-marine molluscs of Argentina
- List of non-marine molluscs of Paraguay
- List of non-marine molluscs of Uruguay
References
[edit]- ^ 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
[edit]- 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.