Planorbidae, Lymnaeidae and Physidae of Ecuador (Mollusca: Basommatophora)

In the course of a trip to Ecuador I had the opportunity of collecting topotypic specimens of the following nominal species of pulmonate molluscs: Biomphalaria cousini Paraense, 1966; Planorbis equatorius Cousin, 1887; P. canonicus Cousin, 1887; Lymnaea cousini Jousseaume, 1887 and P. boetzkesi Miller, 1879. Additional findings were: Helisoma trivolvis (Say, 1817), Biomphalaria peregrina (Orbigny 1835), Drepanotrema anatinum (Orbigny, 1835), D. kermatoides (Orbigny, 1835), D. lucidum (Pfeiffer, 1839), D. surinamense (Clessin, 1884), Lymnaea columella Say, 1817 and Physa acuta Draparnaud, 1805. P. boetzkesi and P. canonicus are considered junior synonyms of Gyraulus hindsianus (Dunker, 1848) and Biomphalaria peregrina (Orbigny, 1835), respectively.     

A bird's eye survey of Central American planorbid molluscs

In the course of two trips to Central America (June 1967 and JulyAugust 1976) I had the opportunity of collecting topotypic specimens of Planorbis nicaraguanus Morelet, 1849, anatomically defined in this paper, and of P. yzabalensis Crosse & Fischer, 1879, the identity of the latter with Drepanotrema anatinum (Orbigny, 1835) is confirmed. The following planorbid species were also found: Helisoma trivolvis (Say, 1817) in Nicaragua, Guatemala, Costa Rica and Belize; H. duryi (Wetherby, 1879) in Costa Rica; Biomphalaria helophila (Orbigny, 1835) in Guatemala, Belize, Nicaragua, Costa Rica and El Salvador; B. kuhniana (Clessin, 1883) in Panama; B. obstructa (Morelet,1849) in Guatemala, Belize and El Salvador; B. straminea (Dunker, 1848) in Costa Rica; B. subprona (Martens, 1899) in Guatemala; D. anatinum (Orbigny,1835) in Belize, Guatemala, Nicaragua and Costa Rica; D. depressissimum (Moricand,1839) in Nicaragua, Costa Rica and Panama; D. lucidum (Pfeiffer, 1839) in Guatemala, Belize and Nicaragua; D. surinamense (Clessin, 1884) in Costa Rica and Panama; and Gyraulus percarinatus sp. n. in Panama. The occurrence of B. kuhniana and D. surinamense is first recorded in Central America, and Gyraulus percarinatus is the first representative of the genus provenly occurring in the American continent south of the United States. The following synonymy is proposed: Planorbis declivis Tate, 1870 = Biomphalaria helophila (Orbigny, 1835); Planorbis isthmicus Pilsbry, 1920 = Biomphalaria kuhniana (Clessin, 1883); Planorbis cannarum Morelet, 1849 and Segmentina donbilli Tristram, 1861 = Biomphalaria obstructa (Morelet, 1849); and Planorbis yzabalensis Crosse & Fischer, 1879 = Drepanotrema anatinum (Orbigny, 1835), confirming Aguayo (1933).     

Planorbidae, lymnaeidae and physidae of Peru (Mollusca: Basommatophora)

In the course of several trips to Peru I had the opportunity of collecting topotypic specimens of Biomphalaria andecola (Orbigny, 1835), B. helophila (Orbigny, 1835), B. pucaraensis (Preston, 1909), Drepanotrema limayanum (Lesson, 1830), D. kermatoides (Orbigny, 1835), and Lymnaea viatrix Orbigny, 1835, besides B. tenagophila (Orbigny, 1835), Helisoma trivolvis (Say, 1817), H. duryi (Wetherby, 1879), Physa acuta Draparnaud, 1801, and seemingly P. peruviana Gray, 1828. B. pucaraensis is considered a junior synonym of B. peregrina (Orbigny, 1835).     

Annotated type catalogue of the Bulimulidae (Mollusca,Gastropoda, Orthalicoidea) in the Natural History Museum,London

The type status is described of 404 taxa classified within the family Bulimulidae (superfamily Orthalicoidea) and kept in the London museum. Lectotypes are designated for Bulimus aurifluus Pfeiffer, 1857; Otostomus bartletti H. Adams, 1867; Helix cactorum d’Orbigny, 1835; Bulimus caliginosus Reeve, 1849; Bulimus chemnitzioides Forbes, 1850; Bulimus cinereus Reeve, 1849; Helix cora d’Orbigny, 1835; Bulimus fallax Pfeiffer, 1853; Bulimus felix Pfeiffer, 1862; Bulimus fontainii d’Orbigny, 1838; Bulimus fourmiersi d’Orbigny, 1837; Bulimus (Mesembrinus) gealei H. Adams, 1867; Bulimus gruneri Pfeiffer, 1846; Bulimus humboldtii Reeve, 1849; Helix hygrohylaea d’Orbigny, 1835; Bulimus jussieui Pfeiffer, 1846; Bulimulus (Drymaeus) binominis lascellianus E.A. Smith, 1895; Helix lichnorum d’Orbigny, 1835; Bulimulus (Drymaeus) lucidus da Costa, 1898; Bulimus luridus Pfeiffer, 1863; Bulimus meleagris Pfeiffer, 1853; Bulimus monachus Pfeiffer, 1857; Bulimus montagnei d’Orbigny, 1837; Helix montivaga d’Orbigny, 1835; Bulimus muliebris Reeve, 1849; Bulimus nigrofasciatus Pfeiffer in Philippi 1846; Bulimus nitelinus Reeve, 1849; Helix oreades d’Orbigny, 1835; Helix polymorpha d’Orbigny, 1835; Bulimus praetextus Reeve, 1849; Bulinus proteus Broderip, 1832; Bulimus rusticellus Morelet, 1860; Helix sporadica d’Orbigny, 1835; Bulimus sulphureus Pfeiffer, 1857; Helix thamnoica var. marmorata d’Orbigny, 1835; Bulinus translucens Broderip in Broderip and Sowerby I 1832; Helix trichoda d’Orbigny, 1835; Bulinus ustulatus Sowerby I, 1833; Bulimus voithianus Pfeiffer, 1847; Bulimus yungasensis d’Orbigny, 1837.The type status of the following taxa is changed to lectotype in accordance with Art. 74.6 ICZN: Bulimulus (Drymaeus) caucaensis da Costa, 1898; Drymaeus exoticus da Costa, 1901; Bulimulus (Drymaeus) hidalgoi da Costa, 1898; Bulimulus (Drymaeus) interruptus Preston, 1909; Bulimulus (Drymaeus) inusitatus Fulton, 1900; Bulimulus latecolumellaris Preston, 1909; Bulimus (Otostomus) napo Angas, 1878; Drymaeus notabilis da Costa, 1906; Drymaeus notatus da Costa, 1906; Bulimulus (Drymaeus) nubilus Preston, 1903; Drymaeus obliquistriatus da Costa, 1901; Bulimus (Drymaeus) ochrocheilus E.A. Smith, 1877; Bulimus (Drymaeus) orthostoma E.A. Smith, 1877; Drymaeus expansus perenensis da Costa, 1901; Bulimulus pergracilis Rolle, 1904; Bulimulus (Drymaeus) plicatoliratus da Costa, 1898; Drymaeus prestoni da Costa, 1906; Drymaeus punctatus da Costa, 1907; Bulimus (Leptomerus) sanctaeluciae E.A. Smith, 1889; Bulimulus (Drymaeus) selli Preston, 1909; Drymaeus subventricosus da Costa, 1901; Bulimulus (Drymaeus) tigrinus da Costa, 1898; Drymaeus volsus Fulton, 1907; Drymaeus wintlei Finch, 1929; Bulimus zhorquinensis Angas, 1879; Bulimulus (Drymaeus) ziczac da Costa, 1898.The following junior subjective synonyms are established: Bulimus antioquensis Pfeiffer, 1855 = Bulimus baranguillanus Pfeiffer, 1853; Drymaeus bellus da Costa, 1906 = Drymaeus blandi Pilsbry, 1897; Bulimus hachensis Reeve 1850 = Bulimus gruneri Pfeiffer, 1846 = Bulimus columbianus Lea, 1838; Bulimus (Otostomus) lamas Higgins 1868 = Bulimus trujillensis Philippi, 1867; Bulimulus (Drymaeus) binominis lascellianus E.A. Smith, 1895 = Bulimulus (Drymaeus) binominis E.A. Smith, 1895; Drymaeus multispira da Costa, 1904 = Helix torallyi d’Orbigny, 1835; Bulimulus (Drymaeus) plicatoliratus Da Costa, 1898 = Bulimus convexus Pfeiffer, 1855; Bulimus sugillatus Pfeiffer, 1857 = Bulimus rivasii d’Orbigny, 1837; Bulimus meridionalis Reeve 1848 [June] = Bulimus voithianus Pfeiffer, 1847.New combinations are: Bostryx montagnei (d’Orbigny, 1837); Bostryx obliquiportus (da Costa, 1901); Bulimulus heloicus (d’Orbigny, 1835); Drymaeus (Drymaeus) lusorius (Pfeiffer, 1855); Drymaeus (Drymaeus) trigonostomus (Jonas, 1844); Drymaeus (Drymaeus) wintlei Finch, 1929; Drymaeus (Mesembrinus) conicus da Costa, 1907; Kuschelenia (Kuschelenia) culminea culminea (d’Orbigny, 1835); Kuschelenia (Kuschelenia) culmineus edwardsi (Morelet, 1863); Kuschelenia (K.) gayi (Pfeiffer, 1857); Kuschelenia (Kuschelenia) tupacii (d’Orbigny, 1835); Kuschelenia (Vermiculatus) anthisanensis (Pfeiffer, 1853); Kuschelenia (Vermiculatus) aquilus (Reeve, 1848); Kuschelenia (Vermiculatus) bicolor (Sowerby I, 1835); Kuschelenia (Vermiculatus) caliginosus (Reeve, 1849); Kuschelenia (Vermiculatus) cotopaxiensis (Pfeiffer, 1853); Kuschelenia (Vermiculatus) filaris (Pfeiffer, 1853); Kuschelenia (Vermiculatus) ochracea (Morelet, 1863); Kuschelenia (Vermiculatus) petiti (Pfeiffer, 1846); Kuschelenia (Vermiculatus) purpuratus (Reeve, 1849); Kuschelenia (Vermiculatus) quechuarum (Crawford, 1939); Naesiotus cinereus (Reeve, 1849); Naesiotus dentritis (Morelet, 1863); Naesiotus fontainii (d’Orbigny, 1838); Naesiotus orbignyi (Pfeiffer, 1846); Protoglyptus pilosus (Guppy, 1871); Protoglyptus sanctaeluciae (E.A. Smith, 1889).Type material of the following taxa is figured herein for the first time: Bulimus cinereus Reeve, 1849; Bulimus coriaceus Pfeiffer, 1857; Bulimulus laxostylus Rolle, 1904; Bulimus pliculatus Pfeiffer, 1857; Bulimus simpliculus Pfeiffer, 1855.     

Phylogenetic relationships and taxonomy of Altiplano populations of Biomphalaria (Gastropoda: Planorbidae): inference from a multilocus approach

Isolated closed basins provide a natural laboratory to study the differentiation among wild populations. Here we examined the phylogenetic relationships of the Southern Altiplano populations of Biomphalaria, a genus with medical importance, using nuclear (ITS1, ITS2) and mitochondrial (16S) ribosomal gene markers and a species of Helisoma as outgroup. Phylogenetic trees based on separate and combined analyses show that these populations form a particular lineage within Biomphalaria along with Biomphalaria peregrina (d'Orbigny, 1835) and Biomphalaria oligoza Paraense, 1974. The origin of this clade was estimated to have occurred in the middle Pleistocene. Molecular analyses showed that the nominal species Biomphalaria crequii ( Courty, 1907 ) from the Salar de Ascotán and Biomphalaria costata (Biese, 1951) from the Salar de Carcote, previously synonymized with Biomphalaria andecola (d'Orbigny, 1835) and B. peregrina, respectively, are distinct taxa. Molecular data did not resolve the relationship of Biomphalaria aymara Valdovinos & Stuardo, 1991 from the Isluga swamps to other Biomphalaria species, but confirm that the populations from the Lauca and Huasco basins may represent a distinct undescribed species of Biomphalaria from the Southern Altiplano. Snails examined for trematodes were found to be positive in some Altiplano localities. © 2012 The Linnean Society of London, Zoological Journal of the Linnean Society, 2012, 165 , 795–808.     

Review of Anhoplocampa Wei (Hymenoptera, Tenthredinidae), with description of a new species and a new combination

Anhoplocampa is redescribed based on new material. Anhoplocampa bicoloricornissp. n. from China is described. Anhoplocampa yunanensis (Haris & Roller, 1999), comb. n. is transferred from Trichiocampus. A key to species of Anhoplocampa is provided. The differences between Anhoplocampa and Trichiocampus Hartig, 1837, Priophorus Dahlbom, 1835, Hoplocampa Hartig, 1837 and Renonerva Wei & Nie, 1998 are briefly discussed.     

Biological control of Biomphalaria tenagophila (Mollusca, Planorbidae), a schistosomiasis vector, using the fish Geophagus brasiliensis (Pisces, Cichlidae) in the laboratory or in a seminatural environment

In order to investigate a possible method of biological control of schistosomiasis, we used the fish Geophagus brasiliensis (Quoy & Gaimard, 1824) which is widely distributed throughout Brazil, to interrupt the life cycle of the snail Biomphalaria tenagophila (Orbigny, 1835), an intermediate host of Schistosoma mansoni. In the laboratory, predation eliminated 97.6% of the smaller snails (3-8 mm shell diameter) and 9.2% of the larger ones (12-14 mm shell diameter). Very promising results were also obtained in a seminatural environment. Studies of this fish in natural snail habitats should be further encouraged.     

Resistance of Biomphalaria occidentalis from Varzea das Flores dam, Minas Gerais, to Schistosoma mansoni infection detected by low stringency polymerase chain reaction

Biomphalaria occidentalis Paraense, 1981 from Varzea das Flores dam, MG, Brazil, was exposed to infection with Schistosoma mansoni. Individual infection was performed with 140 B. occidentalis and 100 B. glabrata snails using LE and SJ strains. Two groups of B. occidentalis were killed after seven day-miracidia exposure to detect S. mansoni DNA, through the low stringency polymerase chain reaction (LS-PCR), and were negative. The infection rates were 69.2% (LE strain) and 96.7% (SJ strain) for B. glabrata and 0% for B. occidentalis. LS-PCR enabled early resistance diagnosis.     

Beyond frontiers and time: the scientific and cultural heritage of Alcide d’Orbigny (1802–1857)

Alcide Dessalines d’Orbigny was born on 6 September 1802 in Couëron (near Nantes), France. In his early youth, he developed a life interest in the study of a group of microscopic animals that he named ‘Foraminifera’. In his first scientific work, devoted to this group, he established the basis of a new science, micropaleontology. All his life, he worked on foraminifera, but his concern in natural sciences widely exceeded the domain of micropaleontology. Impressed by his first work on foraminifera, published at the age of 23, the scientists of the Muséum National d’Histoire Naturelle (MNHN) chose him as the naturalist explorer for an expedition to South America. Alcide d’Orbigny explored Brazil, Argentina, Uruguay, Chile, Bolivia, and Peru from 1826 to 1833. He was a great humanist and applied the view of an ethnologist and historian to the communities with which he shared his daily life in South America. A precursor in biogeography and ecology, he contributed greatly to the advancement of knowledge of the animal and vegetal kingdoms by describing several thousand living species in the nine volumes of his ‘Voyage dans l’Amérique Méridionale’ (1835–1847). Back in France, he turned his research towards paleontology and stratigraphy. He undertook the immense task of describing all species of fossil invertebrates found in France in the eight volumes of ‘La Paléontologie française’ (1840–1860). He arranged 18 000 species in stratigraphic order in the three volumes of ‘Prodrome de Paléontologie stratigraphique’ (1850–1852), and published three volumes entitled ‘Cours élémentaire de paléontologie et de géologie stratigraphiques’ (1849–1852). These important works led him to create the first geological and stratigraphical scale. Many of the 27 stages established are still used in the standard chronostratigraphic scale. The Chair of Paleontology of the MNHN in Paris was created for him in 1853. He died on 30 June 1857 at the age of 55, in Pierrefitte (France), leaving behind him a huge scientific and cultural heritage. Alcide d’Orbigny bequeathed to posterity a collection of more than 100 000 vegetable and animal specimens. This exceptionally rich heritage, deposited in the MNHN, is an international reference collection, and it is actively consulted by specialists from around the world. The application of his work extends to various fields of academic research (such as earth history, paleoceanography and paleoclimatology), to economics and practical applications in stratigraphy and micropaleontology that greatly contribute to oil and other resource exploration as well as major earth construction. The bicentennial of the birth of Alcide d’Orbigny was celebrated in France during the year 2002 under the patronage of the highest authorities of the state, along with scientific and cultural institutions. A traveling exhibition presented the different facets of his life’s work and international congresses were held in the three places dearest to Alcide d’Orbigny: Santa Cruz (Bolivia), La Rochelle (France) and Paris (France). This year (2003) marks the 150th anniversary of his appointment to the Chair of Paleontology of the MNHN.     

Nuclear DNA content in two Sphaeriidae species from Southern Chile (Bivalvia: Veneroida)

The family Sphaeriidae is a group of cosmopolitan freshwater clams that inhabit temporary and permanent fluvial and lacustrine environments around the world. In Chile, Sphaeriidae is represented by 11 species belonging to the genera Musculium, Pisidium and Sphaerium. In this study, the nuclear DNA content (or 2C-value) of Musculium argentinum (d’Orbigny, 1835) and Pisidium llanquihuense Ituarte, 1999 was estimated for the first time. Musculium argentinum showed a 2C-value of 3.7?±?0.38?pg, whereas P. llanquihuense showed a 2C-value of 3.57?±?0.36?pg. These 2C-values are within the range previously reported for Sphaeriidae (2.35–5.7?pg), which includes diploids and polyploids, amounting to 13 of the species examined around the world. Of the cytological data available for the family, the nuclear DNA content can have a unifying role in understanding the magnitude of the chromosome polymorphisms within this polyploid complex.     

Life history of Bulimulus tenuissimus (D'Orbigny, 1835) (Gastropoda,Pulmonata, Bulimulidae): effect of isolation in reproductive strategy and in resources allocation over their lifetime

Despite the great diversity of tropical land snail species, the life history strategies of the great majority of them are unstudied. We studied reproduction, growth and survival patterns of the Brazilian species Bulimulus tenuissimus (D'Orbigny, 1835), and verified the effect of isolation on such patterns. We analyzed aspects of the life cycle of snails maintained in groups and in isolation. For both treatments, we determined the duration of the juvenile, adult and senescent stages. Growth pattern, life-time reproductive output, reproductive output during adult and senescent stages and longevity, were also verified. Isolation prolonged the duration of the juvenile stage, causing a decrease in life-time reproductive output and longevity. The reproductive pattern of the species is seasonal and, in grouped snails, three breeding periods occurred during their lifetime. The isolated snails reproduced by self-fertilization, and only reproduced once in their lifetime, indicating a significant change in reproductive strategy in the isolated individuals. Thus, isolation resulted in changes in energy allocation to growth, reproduction and survival. The results indicate that in adverse environmental conditions, life history traits can enhance the capacity for adaption.     

Malacofauna continental holocena y paleoambientes en Villa Valle María (Diamante, Entre Ríos, Argentina)

The molluscan fauna recovered from Holocene continental sediments at Villa Valle María fossiliferous locality (Diamante, Entre Ríos, Argentina), eolian in origin and dated at 2,490 ± 45 ¹⁴C yrs. B.P. on Bulimulus sp, is reported. It represents the first illustrated record of Quaternary molluscs from loess sequences in Argentina. It is represented exclusively by land snails which belong to five gastropod families (Pupillidae, Succineidae, Ferussaciidae, Orthalicidae and Scolodontidae), 7 genera and 9 species: Gastrocopta nodosaria (d’Orbigny), Succinea meridionalis d’Orbigny, Cecilioides consobrina (d’Orbigny), Bulimulus apodemetes (d’Orbigny), B. bonariensis bonariensis (Rafinesque), Bulimulus sp, Naesiotus pollonerae (Ancey), N. deletangi (Parodiz), Miradiscops brasiliensis (Thiele) and Scolodonta semperi (Doering). The first record of Miradiscops is reported for Entre Ríos province. The gastropod assemblage, typical of habitats with plant cover and leaves and trunks as substrate, is similar to the modern molluscan fauna found today along southern Entre Ríos province (Mesopotamian District in the Subtropical Dominium), an area characterized by a warm-temperate steppe continental scenario. However, the associated record of S. meridionalis, typical of environments with higher humidity contents like ponds, suggests local more humid temporary environmental conditions such as palustrine habitats during the time span considered. Our results provide additional evidence regarding the occurrence of a dominant eolian event which produced the reworking and subsequent accumulation of superficial deflated sediments on the Pampean region. They add to previous models considering a dry period between 3,500 and 1,400 yrs. B.P. over the central Argentine plains.     

Ami Boué (1794–1881), géoscientifique du XIXe siècle

Born on 16 March 1794 in Hamburg as a son of a Huguenot family whose members made big fortune as ship-owners, Ami Boué took his doctor’s degree in medicine in 1817 at the University of Edinburgh. During the following years, he completed his knowledge in the field of natural sciences, especially in Geoscience. In 1830, after having founded, with other scientists, among whom Constant Prévost and Gérard-Paul Deshayes, the Geological Society of France, in which Boué became the first president, he left Paris in 1835 and settled in Vienna. In 1836, 1837 and 1838 he crossed the Balkans. In his masterpiece La Turquie d’Europe (Paris, 1840, four volumes), he published the results of this research. In his study, Ami Boué intended to join the Austrian empire with Turkey by railways. Anyway, Boué’s works concerning the Balkans were fundamental for the future generations of Austrian geoscientists.     

Why Darwin rejected intelligent design

As a Cambridge University undergraduate Charles Darwin was fascinated and convinced by the argument for intelligent design, as set forth in William Paley’s 1802 classic, Natural Theology. Subsequently, during his five-year voyage on HMS Beagle (1831–1836), Darwin interpreted his biological findings through a creationist lens, including the thought-provoking evidence he encountered during his historic visit to the Galápagos Islands in September and October 1835. After his return to England in 1836 and his subsequent conversion to the idea of organic evolution in March 1837, Darwin searched for a theory that would explain both the fact of evolution and the widespread appearance of intelligent design. His insight into the process of natural selection, which occurred in September 1838, provided this alternative explanation. Darwin’s Origin of Species (1859) exemplifies his skillful deployment of the hypothetico-deductive method in testing and refuting the arguments for intelligent design that he had once so ardently admired.     

A Água e o Homem na Várzea do Careiro

Água. o Homem na Várzea do Careiro. Hilgard O'Reily Sternberg. Belém, Brazil: Museu Paraense Emflio Goeldi, 1998. 248 pp.     

Alcide d’Orbigny et la Bolivie (1825–1857)

The evaluation of d’Orbigny’s contribution to Bolivian studies implies putting it in relation with the economic and political context prevailing before, during, and after his travel in this country, between 1830 and 1833. This paper deals with the following topics: the crisis of the silver mines in Potosi, the achievements of the governments of Santa Cruz (1829–1839) and Ballivián (1841–1847), and the various projects intending to open Bolivian lowlands to navigation and colonisation. Finally, some important documents show that d’Orbigny remains concerned with Bolivia many years after he returned to France.