Differences on allocation of available resources, in growth, reproduction, and survival, in an exotic gastropod of Physidae compared to an endemic one

Physa acuta Draparnaud, 1805 is an invasive gastropod that can affect local species. In Argentina, it is widespread and abundant, even in environments inhabited by the native species Stenophysa marmorata Guilding, 1828. Its predominance raises the question whether this could be explained by a more successful energy allocation in functional requirements (growth, reproduction and survival) compared to S. marmorata. This study was aimed at comparing growth rates, as well as survival and fecundity, between both species under laboratory conditions. Individuals born on the same day were grouped in four per aquaria and kept under controlled conditions of food, light, and temperature. Snails were weekly measured (maximum shell length), and growth rates were calculated using the Von Bertalanffy's equation. The number of eggs and survivors were grouped by week. Stenophysa marmorata was larger at birth than Physa acuta and invested more energy in growth, delaying sexual maturity. This resulted in a disadvantage in fecundity and survival compared to P. acuta, which had a lower growth rate but matured earlier and survived longer. Furthermore, the growth of P. acuta was not affected by reproduction, its reproductive period was longer, consequently with more eggs laid than S. marmorata.

Physa Marmorata Guilding, 1828 (Pulmonata: Physidae)

A description of Physa marmorata Guilding, 1828, based on material collected at its type-locality, the Caribbean island of Saint Vincent, is presented. The shell is thin, horn-colored, surface very glossy, diaphanous. Spire acute, elevated; protoconch distinct, rounded-conical, reddish-brown; five not shouldered, broadly convex whorls with subobsolete spiral lines and thin growth lines. Aperture elongated, 1.4-2.0 times as long as the remaining shell length, narrow obovate-lunate; upper half acute-angled,lower half oval,narrowly rounded at the base, outer lip sharp, inner lip completely closing the umbilical region; a very distinct callus on the parietal wall; columellar lip with a low ridge gradually merging into the callus. ratios: shell width/shell length = 0.44 - 0.52 (mean 0.47); spire length /shell lenght = 0.33-0.41 (mean 0.39); aperture length/shell lenght = 0.59-0.67 (mean 0.62). Oral lappets laterally mucronate, foot spatulate with deeply pigmented acuminate tail. Mantle reflection with 6-10 short triangular dentations covering nearly half the right surface of the body whorl, and 4-6 covering a part of the ventral wall. Body surface with tiny dots of greenish-yellow pigment besides melanin. Renal tube tightly folded in toa zigzag course. Ovotestis diverticula acinous, laterally pressed against each other around a collecting canal. Ovispermiduct with well-developed seminal vesicle. oviduct highly convoluted, merging into a less convoluted nidamental gland which narrows to a funnel-shaped uterus and a short vagina. Spermathecal body oblong, more or less constricted in the middle and somewhat curved; spermathecal duct uniformly narrow, a little longer than be body. About 20 prostatic diverticula, simple, bifurcate or divided into a few short branches, distalmost ones assembled into a cluster. Penis long, nearly uniformly narrow; penial canal with lateral opening about the junction of its middle and lower thirds. Penial sheath with a bulbous terminal expasion the tip of which isinserted into the caudal end of the prepuce. Prepuce shouldered, much wider than the narrow portion of the penial sheath. Penial sheath/prepuce ratio about 2.08 (1.45-2.75). The main extrinsic muscles of the penial complex are a retractor, with a branch attached to the bulb, and another to the caudal end of the penial sheath; and a protractor, with a branch attached to the shoulder of the prepuce and adjoining area of the penial sheath, and another to the caudal end of the penial sheath. Egg capsule C-shaped, with 10-30 elliptical eggs (snails 10mm long) measuring about 1.10 mm (0.90-1.32) through the long axis and surrounded by an inner and an outer lamellate membranes. Jaw a simple obtusely V-shaped plate. radula will be described separately.

Physa cubensis Pfeiffer, 1839 (Pulmonata: Physidae)

A description of Physa cubensis Pfeiffer, 1839, based on 15 speciments collected in Havana, Cuba, is presented. The shell, measuring 9.0 x 4,8mm to 12.3 x 6.4mm, is ovate-oblong, thin, diaphanous, horncolored, shining. Spire elevated, broadly conical; protoconch distinct, roundish, reddish-brown. About five moderately shouldered, roundly convex whorls, penultimate whorl expanded; spiral striation subobsolete; growth line faint on the intermediate whorls, clearly visible on the body whorl, crowded here and there. Suture well impressed. Aperture elongated 2.05 - 2.67 (mean 2.27) times as long as the remaining length of the shell, narrow obovulate-lunate; upper half acute-angled, lower half oval, narrowly rounded at the base; outer lip sharp, inner lip completely closing the umbilical region; a thick callus on the parietal wall; columellar plait well marked. Ratios: shell width/shell length - 0.52-0.61 (mean 0.55); spire length/shell length = 0.27 - 0.33 (mean 0.31); aperture length/shell length = 0.67 - 0.73 (mean 0.69). Oral lappets laterally mucronate; foot spatulate with acuminate tail. Mantle relection with 6 - 8 short triangular dentations in the right lobe (columellar side) and 4 - 6 in the left lobe (near the pneumostome). Renal tube tightly folded into a zigzag course. Ovotestis, ovispermiduct, seminal vesicle, oviduct, nidamental gland, uterus and vagina as in Physa marmorata (see Paraense, 1986, Mem. Inst. Oswaldo Cruz, 81: 459-469). Spermathecal body egg-shaped or pear-shaped; spermathecal ducta uniformly narrow with expanded base, a little longer than the body. Spermiduct, prostate and vas deferens as in P. marmorata (Paraense, loc. cit.). Penis wide proximally, narrowing gradually apicad; penial canal with subterminal outlet. Penial sheath following the width of the penis and ending up by a bulbous expansion somewhat narrower than the proximal portion. Penaial sheath/prepuce ration = 1,25 - 1,83 (mean 1.49). Prepuce much wider than the bulb of the penial shealth, moderately shouldered owing to the intromission of the bulb, and with a large gland in one side of its proximal half occupating about a third of its length. Extrinsic muscles of the penial complex as in P. marmorata. Jaw a simple obtusely V-shaped plate. Radula to be described separetely.

Physa acuta Draparnaud, 1805 (Gastropoda: Physidae): a study of topotypic specimens

A description is given of Physa acuta Draparnaud, 1805, based on topotypic specimens from the Garonne river basin, and additional samples from the environs of the French cities of Montpellier and Perpignan. It proved indistinguishable, in shell and anatomy, from topotypic Physa cubensis Pfeiffer, 1839, thus leading the authors to admit the synonymy of the two nominal species under the older name, P. acuta.

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).

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.

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

In the course of several trips to Argentina I had the opportunity of collecting specimens of Acrorbis petricola Odhner,1937, Biomphalaria orbignyi Paraense, 1975, B. peregrina (Orbigny, 1835), B. tenagophila (Orbigny, 1835) Lymnaea viatrix Orbigny, 1835, Antillorbis nordestensis (Lucena, 1954), B. intermedia (Paraense & Deslandes, 1962), B. oligoza Paraense, 1974, B. straminea (Dunker, 1848), Drepanotrema anatinum (Orbigny, 1835), D. cimex (Moricand, 1837), D. depressissimum (Moricand, 1837), D. heloicum (Orbigny, 1835), D. kermatoides (Orbigny, 1835), D. lucidum (Pfeiffer, 1839), L. columella Say, 1817, Physa acuta Draparnaud, 1805, and P. marmorata Guilding, 1828.

Aspectos epidemiológicos da esquistossomose mansônica na região da Represa de Americana, estado de São Paulo, Brasil

Após conhecimento de casos humanos de esquistossomose mansônica supostamente autóctones da Represa de Americana (São Paulo, Brasil) procedeu-se ao estudo epidemiológico da região. Foram constatados seis focos localizados junto à Represa. Foram encontradas as seguintes espécies de moluscos: Biomphalaria tenagophila; B. straminea; B. peregrina; Drepanotrema cimex; D. lucidum; |Lymnaeidae; Ancylidae e Physidae. Exemplares de Biomphalaria tenagophila coletados nos focos apresentaram índices de infecção para cercárias de S. mansoni que variaram de 0,9 a 45%. Mus musculus albinos foram infectados com cercárias no laboratório e nos focos, sendo reproduzido o ciclo do S. mansoni em ambas as condições. Foram registrados 82 casos humanos autóctones de esquistossomose mansônica, na região da Represa de Americana.

Moluscos aquáticos do Estado de Rondônia (Brasil), com especial referência ao gênero Biomphalaria Preston, 1910 (Pulmonata, Planorbidae)

Foi realizado no Estado de Rondônia, Brasil, levantamento malacológico com o objetivo de estabelecer a distribuição geográfica dos moluscos aquáticos, com ênfase especial no gênero Biomphalaria. Foram pesquisados 11 municípios ao longo da rodovia BR-364, totalizando 162 ecossistemas límnicos, dos quais 77 (48%) apresentaram-se positivos para, pelo menos, uma espécie de molusco. As seguintes espécies foram encotradas: Gastropoda, Planorbidae: Biomphalaria sp., B.amazônica, B.occidentalis, Drepanotrema cimex, D.anatinum, D.lucidum e D.depressissimum; Physidae: Stenophysa marmorata; Ancylidae: Gundlachia sp.; Thiaridae: Aylacostoma sp.; Ampullaridae: Pomacea sp.; Pelecypoda, Sphaeriidae: Eupera primei e Pisidium sp. São apresentados dados de distribuição geográfica e discutida a importância epidemiológica dos achados.

Biomphalaria glabrata no Estado do Piauí

É registrado o primeiro encontro do molusco planorbideo Biomphalaria glabrata, hospedeiro intermediário do Schistosoma mansoni, no Estado do Piauí, coletado em vários criadouros na cidade de Parnaíba. O exame de 694 exemplares revelou a presença de formas evolutivas de algumas espécies de trematodeos, mas não de Schistosomatidea. Nenhum caso autoctone de xistosomose foi até agora identificado na população humana da cidade. A presença da B. glabrata em Parnaíba amplia em 20 km para leste a área de sua distribuição na Região Litoral Norte da Grande Região Nordeste do Brasil onde era conhecida até em Avaioses no extremo leste da parte maranhense da referida Região. Outros moluscos também coletados nos mesmos criadouros foram Biomphalaria straminea, Drepanotrema lucidum. D. cimex, D. depressissimum, Physidae e Ampullarriidae.

Comunidade de moluscos bentônicos na área de abrangência da Usina Hidrelétrica de Dona Francisca, Rio Jacuí, Rio Grande do Sul, Brasil : fase de pré e pós-enchimento do reservatório

A malacofauna límnica exerce importante papel como constituinte da comunidade bentônica e alterações em sua estrutura podem tornar-se prejudiciais para a vida nesses ecossistemas. Com o objetivo de avaliar quali-quantitativamente a malacofauna límnica na área de abrangência da Usina Hidrelétrica de Dona Francisca (UHEDF) (29°26’50’’S e 53°16’50’’W), Agudo, Rio Grande do Sul, Brasil, tomadas as amostras nas fases de pré-enchimento do reservatório em oito estações de coleta em áreas localizadas à montante (E3B, E4B, E5B), à jusante (E1) e na calha central do futuro lago da barragem (E2, E3, E4, E5) e pós-enchimento nas estações E1, E3B e E4B. No período de junho a outubro de 2000 (fase de pré-enchimento) e de junho a outubro de 2001 (fase de pós-enchimento) foram realizadas amostragens mensais, consistindo de três réplicas por estação de coleta (margens-centro), através do uso do amostrador de Surber modificado com área de 60 cm² e 15 cm de altura, delimitando o tamanho amostral. A fauna foi retirada manualmente dos clastos maiores sendo o sedimento de granulometria mais fina, passada através de peneira com malha de 1mm. Em laboratório foi realizada a identificação específica dos moluscos e da fauna acompanhante de macroinvertebrados , quando possível até família. Os organismos foram fixados em álcool 70%. Foram identificadas 10 famílias de Mollusca com quinze espécies. Para Gastropoda foram registradas seis famílias com nove espécies: Ampullariidae – Pomacea canaliculata (Lamarck, 1801); Hydrobiidae – Potamolithus aff. catharinae Pilsbry, 1911, Potamolithus ribeirensis Pilsbry, 1911, Potamolithus sp.1 e Heleobia sp.; Chilinidae – Chilina parva Martens, 1868; Lymnaeidae – Lymnaea columella Say, 1817; Ancylidae – Gundlachia concentrica (Orbigny, 1835); e Physidae – Stenophysa marmorata (Guilding, 1938). Para Bivalvia: Corbiculidae – Corbicula fluminea (Müller, 1774); Mycetopodidae – Anodontites iheringi (Clessin, 1882), Anodontites lucidus (Orbigny, 1835); Hyriidae – Diplodon charruanus (Orbigny, 1835); Sphaeriidae – Pisidium punctiferum (Guppy, 1817) e Pisidium sp. Na fase de pré-enchimento do reservatório, a correlação de Pearson apontou correlação positiva entre a granulometria e a densidade de moluscos (r=0,15) e correlação negativa entre os fatores físico-químicos e a densidade de moluscos bentônicos (r=-0,28). A análise de agrupamento das espécies de moluscos na fase de pré-enchimento evidenciou a formação de dois grupos distintos: o primeiro formado por espécies acidentais, segundo o cálculo da Constância, e o segundo formado por espécies constantes, xviii acessórias e uma acidental (Potamolithus sp.1) que no entanto foi abundante em E1 e E2. O resultado da freqüência relativa em relação à fase de pré-enchimento do reservatório mostrou a família Hydrobiidae, com quatro espécies, com maior abundância e riqueza de espécies, seguida por Chilinidae, representada por C. parva. Ambas as famílias representaram um total de 93,9% em relação à comunidade de moluscos amostrados. Tais resultados refletem o tipo de ambiente da área: leito formado por matacões e calhaus, favoráveis à instalação e manutenção daqueles moluscos. Na fase de pós-enchimento do reservatório foram registrados o aumento na riqueza e diversidade de espécies nas três estações de coleta amostradas (exceto em E3B – com menor diversidade no pós-enchimento) e diminuição significativa nas densidades mensais e totais de moluscos bentônicos. Os testes de aleatorização, entretanto, não revelaram diferenças significativas entre as duas fases e em relação ao funcionamento da UHEDF. Os fatores físico-químicos apontaram correlação positiva com a densidade de moluscos (r=0,19), ressaltando as diferenças significativas nos valores de pH, oxigênio dissolvido, oxigênio saturado nesta fase. Em E1 mais atingida pelo funcionamento da UHEDF, registrou-se uma acentuada diminuição nas densidades mensais e totais de moluscos bentônicos, não obstante, a riqueza e diversidade apresentaram maiores valores nesta fase. As espécies mantiveram-se as mesmas em ambas as fases.

Physa mezzalirai, a new cretaceous basommatophoran from Adamantina formation, Brazil.

This paper deals with a formal description of Physa mezzalirai (Basommatophora, Physidae), a new species of freshwater gastropod that lived in upper Cretaceous deposits, in sand-silty beds of Adamantina formation, Bauru basin, from Marlia, São Paulo state, Brazil. This formal description legitimates the availability of the name previously described in 2010 by same authors; being this paper the correct citation for the species name.

Physa mezzalirai: um novo gastrópode da formação Adamantina (Bacia Bauru), Cretáceo Superior, São Paulo, Brasil

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Macroinvertebrate abundance and proportion of trait categories in river biotopes across England and Wales

There is a long tradition of river monitoring using macroinvertebrate communities to assess environmental quality in Europe. A promising alternative is the use of species life-history traits. Both methods, however, have relied on the time-consuming identification of taxa. River biotopes, 1-100 m**2 'habitats' with associated species assemblages, have long been seen as a useful and meaningful way of linking the ecology of macroinvertebrates and river hydro-morphology and can be used to assess hydro-morphological degradation in rivers. Taxonomic differences, however, between different rivers had prevented a general test of this concept until now. The species trait approach may overcome this obstacle across broad geographical areas, using biotopes as the hydro-morphological units which have characteristic species trait assemblages. We collected macroinvertebrate data from 512 discrete patches, comprising 13 river biotopes, from seven rivers in England and Wales. The aim was to test whether river biotopes were better predictors of macroinvertebrate trait profiles than taxonomic composition (genera, families, orders) in rivers, independently of the phylogenetic effects and catchment scale characteristics (i.e. hydrology, geography and land cover). We also tested whether species richness and diversity were better related to biotopes than to rivers. River biotopes explained 40% of the variance in macroinvertebrate trait profiles across the rivers, largely independently of catchment characteristics. There was a strong phylogenetic signature, however. River biotopes were about 50% better at predicting macroinvertebrate trait profiles than taxonomic composition across rivers, no matter which taxonomic resolution was used. River biotopes were better than river identity at explaining the variability in taxonomic richness and diversity (40% and <=10%, respectively). Detailed trait-biotope associations agreed with independent a priori predictions relating trait categories to near river bed flows. Hence, species traits provided a much needed mechanistic understanding and predictive ability across a broad geographical area. We show that integration of the multiple biological trait approach with river biotopes at the interface between ecology and hydro-morphology provides a wealth of new information and potential applications for river science and management.