Alimentação do peixe-rei (Odontesthes bonariensis, Atherinopsidae) nas lagoas Mirim e Mangueira, Rio Grande do Sul, Brasil

Foi estudada a alimentação natural do peixe-rei (Odontesthes bonariensis Cuvier & Valenciennes, 1835) nas lagoas Mirim e Mangueira, Estado do Rio Grande do Sul, Brasil. O conteúdo estomacal de 60 indivíduos de peixe-rei (Odontesthes bonariensis) provenientes dessas lagoas mostraram que esta espécie tem amplo espectro alimentar. Uma grande variedade de alimentos é consumida, sem afetar o crescimento, pois os peixes dos dois ambientes apresentaram condição corporal semelhante. Na lagoa Mangueira, crustáceos (Isopoda) representaram 65% da dieta dos peixes e na lagoa Mirim, moluscos (Bivalvia e Gastropoda) perfizeram 70% dos conteúdos de estômago identificados.

Benthic macroinvertebrates as bioindicators of water quality in an Atlantic forest fragment

The objective of this study was to evaluate benthic macroinvertebrate communities as bioindicators of water quality in five streams located in the "Reserva Particular do Patrimônio Natural" (RPPN) Mata Samuel de Paula and its surroundings, in the municipality of Nova Lima near the city of Belo Horizonte, Minas Gerais State, southeastern Brazil. This region has been strongly modified by human activities including mining and urbanization. Samples were collected in the field every three months between August 2004 and November 2005, totaling six samplings in the rainy and dry seasons. This assessment identified one area ecologically altered while the other sampling sites were found to be minimally disturbed systems, with well-preserved ecological conditions. However, according to the Biological Monitoring Work Party (BMWP) and the Average Score Per Taxon (ASPT) indices, all sampling sites had excellent water quality. A total of 14,952 organisms was collected, belonging to 155 taxa (148 Insecta, two Annelida, one Bivalvia, one Decapoda, one Planariidae, one Hydracarina, and one Entognatha). The most abundant benthic groups were Chironomidae (47.9%), Simuliidae (12.3%), Bivalvia (7.5%), Decapoda (6.1%), Oligochaeta (5.2%), Polycentropodidae (3.7%), Hydropsychidae (2.5%), Calamoceratidae (1.8%), Ceratopogonidae (1.7%), and Libellulidae (1.2%). The assessment of the benthic functional feeding groups showed that 34% of the macroinvertebrates were collector-gatherers, 29% predators, 24% collector-filterers, 8% shredders, and 5% scrapers. The RPPN Mata Samuel de Paula comprises diversified freshwater habitats that are of great importance for the conservation of many benthic taxa that are intolerant to organic pollution.

Trophic relationships between macroinvertebrates and fish in a pampean lowland stream (Argentina)

The diet and trophic relationships between the macroinvertebrates Phyllogomphoides joaquini Rodrigues Capítulo, 1992 and Coenagrionidae (Odonata), Chironomidae (Diptera), Diplodon delodontus (Lamarck, 1919) (Bivalvia: Hyriidae), and Pomacea canaliculata (Lamarck, 1822) (Gastropoda: Ampulariidae) and the fishes Pimelodella laticeps Eigenmann, 1917 (Heptapteridae) and Bryconamericus iheringii (Boulenger, 1887) (Characidae) in a temperate lowland lotic system in Argentina were assessed on the basis of gut contents and stable-isotope analyses. The feeding strategies were analyzed by the AMUNDSEN method. Relative food items contribution for the taxa studied indicated a generalist-type trophic strategy. In macroinvertebrates, in general, the values of stable isotope confirmed the result of the analysis of gut contents. With the fish, stable-isotope analysis demonstrated that both species are predators, although B. iheringii exhibited a more omnivorous behaviour. These feeding studies allowed us to determine the trophic relationships among taxa studied. Detritus and diatoms were a principal source of food for all the macroinvertebrates studied. In La Choza stream the particulate organic matter is a major no limited food resource, has a significant influence upon the community.

Levantamento preliminar de moluscos em praias arenosas e areno-lodosas de Piúma, estado do Espírito Santo, Brasil

The present work is a preliminary contribution to the knowledge of the fauna, with regard to the aspect of mullusks, on the coast located in the city of Piúma (40º45' lat. L and 20º50' long. W) Espírito Santo State, aiming a better comprehension of the distribution and ecology of mollusks in the South Atlantic. Collections were made in planned sporadic periods (May/29 to 31 of 1984; May/04-05 and September/13-16 of 1985; March/26-28; October/30-31 and November/01-02 of 1986), in the intertidal zones in the area, in each chosen region and in presence of an 0.0 tide. The material identified by comparative analysis of the morphologic variability presented a total of 41 generic taxa (52.56%) and 44 specific taxa (52.38%) of the class Gastropoda, 36 generic taxa (46.15%) and 39 specific taxa (46.43%) of the class Bivalvia and 1 generic taxa (1,28%) and 1 specific taxa (1.19%) of the class Scaphopoda.

Boring activity of Epibionts in an Early Holocene molluscan fauna of Spanish Catalunya

Using X-Ray techniques, the boring activities of various Invertebrates on Bivalvia of wmian age were studied. Emphasis is placed on the boring activity of Porifera and their apparent preselection of the species bored, based on: a) the mineralogical composition, and/or b) the microstucture, andlor c) some special environmental conditions, or d) combinations of these three posibilities.

Segunda adición a la fauna malacológica del litoral del Garraf (NE de la Península Ibérica)

Se presenta una tercera lista de 68 especies de moluscos marinos (4 Caudofoveata, 1 Solenogastre, 32 Gastropoda, 15 Bivalvia y 16 Cephalopoda) que no habían sido citados anteriormente en ahuas del litoral del Garraf (Barcelona, NE de la Península Ibérica).

Species 2000 & ITIS Catalogue of Life, 2013 Annual Checklist

This release of the Catalogue of Life contains contributions from 132 databases with information on 1,352,112 species, 114,069 infraspecific taxa and also includes 928,147 synonyms and 408,689 common names covering the following groups: Viruses • Viruses and Subviral agents from ICTV_MSL UPDATED! Bacteria and Archaea from BIOS Chromista • Chromistan fungi from Species Fungorum Protozoa • Major groups from ITIS Regional, • Ciliates from CilCat, • Polycystines from WoRMS Polycystina UPDATED!, • Protozoan fungi from Species Fungorum and Trichomycetes database • Slime moulds from Nomen.eumycetozoa.com Fungi • Various taxa in whole or in part from CABI Bioservices databases (Species Fungorum, Phyllachorales, Rhytismatales, Saccharomycetes and Zygomycetes databases) and from three other databases covering Xylariaceae, Glomeromycota, Trichomycetes, Dothideomycetes • Lichens from LIAS UPDATED! Plantae (Plants) • Mosses from MOST • Liverworts and hornworts from ELPT • Conifers from Conifer Database • Cycads and 6 flowering plant families from IOPI-GPC, and 99 families from WCSP • Plus individual flowering plants families from AnnonBase, Brassicaceae, ChenoBase, Droseraceae Database, EbenaBase, GCC UPDATED!, ILDIS UPDATED!, LecyPages, LHD, MELnet UPDATED!, RJB Geranium, Solanaceae Source, Umbellifers. Animalia (Animals) • Marine groups from URMO, ITIS Global, Hexacorals, ETI WBD (Euphausiacea), WoRMS: WoRMS Asteroidea UPDATED!, WoRMS Bochusacea UPDATED!, WoRMS Brachiopoda UPDATED!, WoRMS Brachypoda UPDATED!, WoRMS Brachyura UPDATED!, WoRMS Bryozoa UPDATED!, WoRMS Cestoda NEW!, WoRMS Chaetognatha UPDATED!, WoRMS Cumacea UPDATED!, WoRMS Echinoidea UPDATED!, WoRMS Gastrotricha NEW!, WoRMS Gnathostomulida NEW!, WoRMS Holothuroidea UPDATED!, WoRMS Hydrozoa UPDATED!, WoRMS Isopoda UPDATED!, WoRMS Leptostraca UPDATED!, WoRMS Monogenea NEW!, WoRMS Mystacocarida UPDATED!, WoRMS Myxozoa NEW!, WoRMS Nemertea UPDATED!, WoRMS Oligochaeta UPDATED!, WoRMS Ophiuroidea UPDATED!, WoRMS Phoronida UPDATED!, WoRMS Placozoa NEW!, WoRMS Polychaeta UPDATED!, WoRMS Polycystina UPDATED!, WoRMS Porifera UPDATED!, WoRMS Priapulida NEW!, WoRMS Proseriata and Kalyptorhynchia UPDATED!, WoRMS Remipedia UPDATED!, WoRMS Scaphopoda UPDATED!, WoRMS Tanaidacea UPDATED!, WoRMS Tantulocarida UPDATED!, WoRMS Thermosbaenacea UPDATED!, WoRMS Trematoda NEW!, WoRMS Xenoturbellida UPDATED! • Rotifers, mayflies, freshwater hairworms, planarians from FADA databases: FADA Rotifera UPDATED!, FADA Ephemeroptera NEW!, FADA Nematomorpha NEW! & FADA Turbellaria NEW! • Entoprocts, water bears from ITIS Global • Spiders, scorpions, ticks & mites from SpidCat via ITIS UPDATED!, SalticidDB , ITIS Global, TicksBase, SpmWeb BdelloideaBase UPDATED! & Mites GSDs: OlogamasidBase, PhytoseiidBase, RhodacaridBase & TenuipalpidBase • Diplopods, centipedes, pauropods and symphylans from SysMyr UPDATED! & ChiloBase • Dragonflies and damselflies from Odonata database • Stoneflies from PlecopteraSF UPDATED! • Cockroaches from BlattodeaSF UPDATED! • Praying mantids from MantodeaSF UPDATED! • Stick and leaf insects from PhasmidaSF UPDATED! • Grasshoppers, locusts, katydids and crickets from OrthopteraSF UPDATED! • Webspinners from EmbiopteraSF UPDATED! • Bark & parasitic lices from PsocodeaSF NEW! • Some groups of true bugs from ScaleNet, FLOW, COOL, Psyllist, AphidSF UPDATED! , MBB, 3i Cicadellinae, 3i Typhlocybinae, MOWD & CoreoideaSF NEW!• Twisted-wing parasites from Strepsiptera Database UPDATED! • Lacewings, antlions, owlflies, fishflies, dobsonflies & snakeflies from LDL Neuropterida • Some beetle groups from the Scarabs UPDATED!, TITAN, WTaxa & ITIS Global • Fleas from Parhost • Flies, mosquitoes, bots, midges and gnats from Systema Dipterorum, CCW & CIPA • Butterflies and moths from LepIndex UPDATED!, GloBIS (GART) UPDATED!, Tineidae NHM, World Gracillariidae • Bees & wasps from ITIS Bees, Taxapad Ichneumonoidea, UCD, ZOBODAT Vespoidea & HymIS Rhopalosomatidae NEW!• Molluscs from WoRMS Mollusca NEW!, FADA Bivalvia NEW!, MolluscaFW NEW! & AFD (Pulmonata) • Fishes from FishBase UPDATED! • Reptiles from TIGR Reptiles • Amphibians, birds and mammals from ITIS Global PLUS additional species of many groups from ITIS Regional, NZIB and CoL China NEW!

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.

Permian non-marine bivalves of the Falkland Islands and their palaeoenvironmental significance

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

TAXONOMIC POSITION of GUIRATINGIA MENDESI (MEGADESMIDAE) and THE EVOLUTION of PERMIAN ENDEMIC BIVALVE FAUNA of THE PARANA BASIN, BRAZIL

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

Shell beds as paleoecological puzzles: A case study from the Upper Permian of the Parana Basin, Brazil

Microstratigraphic, sedimentological, and taphonomic features of the Ferraz Shell Bed, from the Upper Permian (Kazanian-Tatarian?) Corumbatai Formation of Rio Claro Region (the Parana Basin, Brazil), indicate that the bed consists of four distinct microstratigraphic units. They include, from bottom to top, a lag concentration (Unit 1), a partly reworked storm deposit (Unit 2), a rapidly deposited sandstone unit with three thin horizons recording episodes of reworking (Unit 3), and a shell-rich horizon generated by reworking/winnowing that was subsequently buried by storm-induced obrution deposit (Unit 4). The bioclasts of the Ferraz Shell Bed represent exclusively bivalve mollusks. Pinzonella illusa and Terraia aequilateralis are the dominant species. Taphonomic analysis indicates that mollusks are heavily time-averaged (except for some parts of Unit 3). Moreover, different species are time-averaged to a different degree (disharmonious time-averaging). The units differ statistically from one another in their taxonomic and ecological composition, in their taphonomic pattern, and in the size-frequency distributions of the two most common species. Other Permian shell beds of the Parana Basin are similar to the Ferraz Shell Bed in their faunal composition (they typically contain similar sets of 5 to 10 bivalve species) and in their taphonomic, sedimentologic, and microstratigraphic characteristics. However, rare shell beds that include 2-3 species only and are dominated by articulated shells preserved in life position also occur. Diversity levels in the Permian benthic associations of the Parana Basin were very low, with the point diversity of 2-3 species and with the within-habitat and basin-wide (alpha and gamma) diversities of 10 species, at most. The Parana Basin benthic communities may have thus been analogous to low-diversity bivalve-dominated associations of the present-day Baltic Sea. The 'Ferraz-type' shell beds of the Parana Basin represent genetically complex and highly heterogeneous sources of paleontological data. They are cumulative records of spectra of benthic ecosystems time-averaged over long periods of time (10(2)-10(4) years judging from actualistic research). Detailed biostratinomic reconstructions of shell beds can not only offer useful insights into their depositional histories, but may also allow paleoecologists to optimize their sampling designs, and consequently, refine paleoecological and paleoenvironmental interpretations.

Permian bivalve molluscs from the Gai-As Formation, northern Namibia: systematics, taphonomy and biostratigraphy

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

Invertebrates from the Low Head Member (Polonez Cove Formation, Oligocene) at Vaureal Peak, King George Island, West Antarctica

Eight taxa of marine invertebrates, including two new bivalve species, are described from the Low Head Member of the Polonez Cove Formation (latest early Oligocene) cropping out in the Vaureal Peak area, King George Island, West Antarctica. The fossil assemblage includes representatives of Brachiopoda (genera Neothyris sp. and Liothyrella sp.), Bivalvia (Adamussium auristriatum sp. nov., ?Adamussium cf. A. alanbeui Jonkers, and Limatula (Antarctolima) ferraziana sp. nov.), Bryozoa, Polychaeta (serpulid tubes) and Echinodermata. Specimens occur in debris flows deposits of the Low Head Member, as part of a fan delta setting in a high energy, shallow marine environment. Liothyrella sp., Adamussium auristriatum sp. nov. and Limatula ferraziana sp. nov. are among the oldest records for these genera in King George Island. In spite of their restrict number and diversification, bivalves and brachiopods from this study display an overall dispersal pattern that roughly fits in the clockwise circulation of marine currents around Antarctica accomplished in two steps. The first followed the opening of the Tasmanian Gateway at the Eocene/Oligocene boundary, along the eastern margin of Antarctica, and the second took place in post-Palaeogene time, following the Drake Passage opening between Antarctic Peninsula and South America, along the western margin of Antarctica.