Mechanistic study of arsenic uptake, transformation and tolerance in arsenic hyperaccumulator Pteris vittata

Pteris vittata, the first reported arsenic hyperaccumulating plant, is potentially used in phytoremediation of arsenic, as it can accumulate up to 2.3% of arsenic in its fronds. In this study, the mechanisms of arsenic tolerance, uptake and transformation were studied in the plant. Arsenic species were analyzed by HPLC-AFS. Results showed that arsenic was mainly accumulated in leaflets, and inorganic arsenate and arsenite were only species in P. vittata. Arsenite was the predominant species in leaflets, whereas arsenate was the predominant species in roots. Arsenic induced the synthesis of thiol containing compounds in P. vittata. As-induced thiol was purified by a novel method: covalent chromatography following preparative HPLC. The purified thiol was characterized as a phytochelatin with two units (PC2). ^ In P. vittata, enhanced tolerance likely results from unusual intracellular detoxification mechanisms. Although PC-dependent sequestration of arsenic into vacuoles is essential for nonhyperaccumulators, this sequestration is not the major arsenic tolerance mechanisms in this arsenic hyperaccumulator. PC-independent sequestration of arsenic is likely the major arsenic tolerance mechanism. PC-dependent arsenic detoxification is probably a supplement to this major mechanism. ^ Interactions between arsenic and phosphate were studied. Under hydroponic condition, arsenic supply decreased the concentrations of phosphate in roots. In soil, arsenic increased the concentrations of phosphate in roots. Arsenic concentrations in rachises and leaflets were not affected by arsenic supply in either hydroponic or soil system. Phosphate decreased arsenic accumulation in roots, rachises and leaflets in the hydroponic system. ^ The uptake kinetics of arsenate, arsenite, monomethyl arsinic acid (MMA), dimethyl arsonic acid, and phosphate were studied in P. vittata. Phosphate uptake systems in Pteris vittata cannot distinguish phosphate and As(V), resulting in As hyperaccumulation. Arsenic hyperaccumulation in this plant is an inevitable consequence during phosphate acquisition. Arsenate, arsenite and MMA are transported via the phosphate uptake systems. The co-transport of arsenite/phosphate and MMA/phosphate is reported for the first time in plants. These unique phenomena are useful for understanding arsenic hyperaccumulation and the evolution of this capacity in P. vittata. ^

Epigean and subterranean ichthyofauna in Cordisburgo karst area, eastern Brazil

After an ichthyofaunistic survey conducted in May 2007 on surface (epigean) water bodies of Cordisburgo karst area, State of Minas Gerais, 13 species were recorded, mostly characiforms; in addition three non-troglomorphic (normally eyed and pigmented) and one troglomorphic catfish (siluriforms) species were recorded in two caves surveyed at different occasions, totaling 17 fish species for the area. All the nominal species herein reported for Cordisburgo area have been previously reported for the Rio das Velhas basin. None of the species observed in caves were found in epigean habitats and vice-versa. The four cave species are distributed throughout subterranean stream reaches, with individuals at different size/age classes. This, associated to the lack of conspicuous morphological differences in relation to epigean congeners, indicate that Trichomycterus brasiliensis, Gymnotus cf. carapo and Pimelodella cf. vittata are troglophiles (species encompassing individuals able to live and complete their life cycle either in the surface or in the subterranean environment) in the Morena Cave; the latter forms a large population and may be at the beginning of a differentiation process due to isolation in the subterranean habitat, as indicated by a slight reduction in eye size. Topographic isolation may be the cause for the incipient, but unmistakable troglomorphism of the Rhamdiopsis population found in the Salitre Cave, allowing for its classification as troglobite (exclusively subterranean species). The Cordisburgo area is subject to significant anthropic pressure, mainly represented by deforestation for agriculture, cattle raising and timbering. Tourism is an additional important threat for cave communities, calling for urgent protection measures.

Male sleeping aggregations of solitary oil-collecting bees in Brazil (Centridini, Tapinotaspidini, and Tetrapediini; Hymenoptera: Apidae)

Males of solitary bees usually spend the night in clusters on small branches of plants, cavities and flowers. The individuals usually return to the same location each evening during their life, exhibiting site fidelity to a particular plant. We report on the sleeping roosts of the males of some oil-collecting bees of the genera Centris, Paratetrapedia, Lanthanomelissa, Monoeca, and Tetrapedia, as well as the host plants. We discuss the role of the male clusters to the associated plants.

Status of Early 19th-Century Names Authored in Parallel by Wied and Schinz for South American Reptiles and Amphibians, with Designations of Three Nomina Protecta

Prince Maximilian zu Wied's great exploration of coastal Brazil in 1815-1817 resulted in important collections of reptiles, amphibians, birds, and mammals, many of which were new species later described by Wied himself The bulk of his collection was purchased for the American Museum of Natural History in 1869, although many ""type specimens"" had disappeared earlier. Wied carefully identified his localities but did not designate type specimens or type localities, which are taxonomic concepts that were not yet established. Information and manuscript names on a fraction (17 species) of his Brazilian reptiles and amphibians were transmitted by Wied to Prof. Heinrich Rudolf Schinz at the University of Zurich. Schinz included these species (credited to their discoverer ""Princ. Max."") in the second volume of Das Thierreich ... (1822). Most are junior objective synonyms of names published by Wied. However, six of the 17 names used by Schinz predate Wied's own publications. Three were manuscript names never published by Wied because he determined the species to be previously known. (1) Lacerta vittata Schinz, 1822 (a nomen oblitum) = Lacerta striata sensu Wied (a misidentification, non Linnaeus nec sensu Merrem) = Kentropyx calcarata Spix, 1825, herein qualified as a nomen protectum. (2) Polychrus virescens Schinz, 1822 = Lacerta marmorata Linnaeus, 1758 (now Polychrus marmoratus). (3) Scincus cyanurus Schinz, 1822 (a nomen oblitum) = Gymnophthalmus quadrilineatus sensu Wied (a misidentification, non Linnaeus nec sensu Merrem) = Micrablepharus maximiliani (Reinhardt and Lutken, ""1861"" [1862]), herein qualified as a nomen protectum. Qualifying Scincus cyanurus Schinz, 1822, as a nomen oblitum also removes the problem of homonymy with the later-named Pacific skink Scincus cyanurus Lesson (= Emoia cyanura). The remaining three names used by Schinz are senior objective synonyms that take priority over Wied's names. (4) Bufo cinctus Schinz, 1822, is senior to Bufo cinctus Wied, 1823; both, however, are junior synonyms of Bufo crucifer Wied, 1821 = Chaunus crucifer (Wied). (5) Agama picta Schinz, 1822, is senior to Agama picta Wied, 1823, requiring a change of authorship for this poorly known species, to be known as Enyalius pictus (Schinz). (6) Lacerta cyanomelas Schinz, 1822, predates Teius cyanomelas Wied, 1824 (1822-1831) both nomina oblita. Wied's illustration and description shows cyanomelas as apparently conspecific with the recently described but already well-known Cnemidophorus nativo Rocha et al., 1997, which is the valid name because of its qualification herein as a nomen protectum. The preceding specific name cyanomelas (as corrected in an errata section) is misspelled several ways in different copies of Schinz's original description (""cyanom las,"" ""cyanomlas,"" and cyanom""). Loosening, separation, and final loss of the last three letters of movable type in the printing chase probably accounts for the variant misspellings.

Influence of Redox Environments on the Solubility of Arsenic in Soils

Arsenic (As) is a semimetallic element that is notorious for its toxicity and carcinogenicity. Arsenic can be removed by some ferns. The objectives of this study were to investigate the ability of Pteris vittata L. (Pteridophyta) and Phlebodium aureum (L.) J. Sm. (Polypodiaceae) to absorb inorganic As, in the form of arsenate and arsenite. The removal of As by ferns was observed at varying anion concentrations and As solubility in the absorbing plant. Results obtained with ferns on As-contaminated soil indicate that redox potential and iron (Fe) presence affected the solubility of As and the absorption capacity of ferns. Upon reduction to -200mV, the soluble As content increased to 400mV. The results indicate that Fe oxides and the influence of redox potential strongly affect As absorption. Under nonreducing conditions, Phlebodium aureum did not remove As as well as Pteris vittata. Under more reducing conditions (-200 to 0mV) and under similar soil conditions, the results show that the both ferns remove As.

Reproductive biology of Cyrtopodium polyphyllum (Orchidaceae): a Cyrtopodiinae pollinated by deceit

The genus Cyrtopodium comprises about 42 species distributed from southern Florida to northern Argentina. Cyrtopodium polyphyllum occurs on rocks or in sandy soils, in restinga vegetation along the Brazilian coast. It flowers during the wet season and its inflorescences produce a high number of resupinate yellow flowers. Cyrtopodium polyphyllum offers no rewards to its pollinators, but mimics the yellow, reward-producing flowers of nearby growing Stigmaphyllon arenicola (oil) and Crotalaria vitellina (nectar) individuals. Several species of bee visit flowers of C. polyphyllum, but only two species of Centris (Centris tarsata and Centris labrosa) act as pollinators. Visits to flowers of C. polyphyllum were scarce and, as a consequence, low-fruit set was recorded under natural conditions. Such low-fruit production contrasts with the number of fruits each plant bears after manual pollination, suggesting deficient pollen transfer among plants. C. polyphyllum is self-compatible and has a high-fruit set in both manual self- and cross-pollinated flowers. Furthermore, fruits (2%) are formed by self-pollination assisted by rain. This facultative self-pollination mechanism is an important strategy to provide reproductive assurance to C. polyphyllum as rainfall restricts the foraging activity of its pollinating bees. Fruits derived from treatments and under natural conditions had a similar high rate of potentially viable seed. Moreover, these seeds had a low polyembryony rate, which did not exceed 5%. C. polyphyllum acts by deceit involving optical signals and exploits other yellow-flowered species within its habitat by attracting their pollinators. The low capsule production under natural conditions was expected, but its reproductive success is assured through self-pollination by rain and high seed viability.

Molecular detection of Paracoccidioides brasiliensis in road-killed wild animals

Paracoccidioides brasiliensis infections have been little studied in wild and/or domestic animals, which may represent an important indicator of the presence of the pathogen in nature. Road-killed wild animals have been used for surveillance of vectors of zoonotic pathogens and may offer new opportunities for eco-epidemiological studies of paracoccidiodomycosis (PCM). The presence of P. brasiliensis infection was evaluated by Nested-PCR in tissue samples collected from 19 road-killed animals; 3 Cavia aperea (guinea pig), 5 Cerdocyon thous (crab-eating-fox), 1 Dasypus novemcinctus (nine-banded armadillo), 1 Dasypus septemcinctus (seven-banded armadillo), 2 Didelphis albiventris (white-eared opossum), 1 Eira barbara (tayra), 2 Gallictis vittata (grison), 2 Procyon cancrivorus (raccoon) and 2 Sphiggurus spinosus (porcupine). Specific P. brasiliensis amplicons were detected in (a) several organs of the two armadillos and one guinea pig, (b) the lung and liver of the porcupine, and (c) the lungs of raccoons and grisons. P. brasiliensis infection in wild animals from endemic areas might be more common than initially postulated. Molecular techniques can be used for detecting new hosts and mapping `hot spot` areas of PCM.

Reproductive biology of Bellucia (MELASTOMATACEAE)

The reproductive biology of five of the seven species of Bellucia (Melastomataceae), a genus of shrubs and small trees, was investigated in Amazonia. Sucessful fruit-set by Bellucia requires floral visitation by bees. The flowers are produced continuously all year, and are visited by a wide variety of female bees, the principal pollinators being Xylocopa, Centris, Ptilotopus, Epicharis, Eulaema, Bombus, and Oxaea. The floral attractants are color and the odor produced by the pollen, stamens, and petals; the reqard is pollen. Three species of Bellucia are self-incompatible. Indiscriminate visitor behavior and lack of phenological, morphological, or genetic barriers lead to hybridization between sympatric species of Bellucia, and no more than two species occupy the same habitat at anu one locality. Bellucia produces berries with numerous small seeds, and is dispersed by birds, bats, monkeys, tapirs, turtles, and ants. Seedling establisment requires full sunlight, and occurs on a variety of soil types. The reproductive strategy is interpreted as that of a pioneer species.

Diversidade de abelhas (Hymenoptera: Apoidea) em uma área de transição Cerrado-Amazônia

A comunidade de abelhas em uma área de transição cerrado-amazônia, localizada na região do Bico-do-Papagaio, Estado do Tocantins, foi estudada entre novembro de 1999 e novembro de 2000, por meio da amostragem sistemática dos espécimes nas plantas em floração, com o objetivo de obter informações sobre a sua composição. Um total de 5.534 indivíduos, distribuídos em 83 espécies e 38 gêneros foram coletados. A maior abundância de indivíduos e riqueza de espécies foi encontrado na família Apidae sensu Roig-Alsina & Michener. Os gêneros com maior riqueza foram Trigona (8), Megachile (7), Centris (6), Augochloropsis (5), Coelioxys (5), Paratetrapedia (5) e Xylocopa (5), enquanto que a espécie mais freqüente foi Apis mellifera. A comunidade seguiu o padrão geral encontrado nos neotrópicos, apresentando muitas espécies com poucos indivíduos e poucas espécies com muitos indivíduos. A freqüência, constância e dominância das espécies são discutidas e os índices de abundância, diversidade, eqüitabilidade e dominância são apresentados.

Biologia floral e sistema reprodutivo de Byrsonima coccolobifolia (Kunth) em uma savana amazônica

A biologia reprodutiva de Byrsonima coccolobifolia, foi avaliada em uma população de savana do Estado de Roraima. A espécie é constituída de arbustos e arvoretas com altura inferior a 3m, de flores hermafroditas zigomorfas, pentâmeras, reunidas em inflorescências do tipo racemo terminal, produzidos em brotações novas, o cálice é composto por cinco sépalas, que apresentam um par de glândulas produtoras de óleo. A corola é formada por cinco pétalas albo-róseas e unguiculadas, o androceu é composto por dez estames com anteras de coloração amarela. A antese pode ser noturna ou diurna, estende-se por um período médio de 12 horas e as flores costumam ficar abertas e vistosas por um período adicional de 15 horas, quando se inicia a senescência. Foram registrados dois episódios de floração e o fogo parece ser um fator ambiental estimulador desta fenofase. Os visitantes florais predominantes foram abelhas das famílias Anthophoridae (Centris sp. e Xylocopa sp.) e Apidae (Apis mellifera e Bombus sp.). Os resultados das polinizações controladas e o cálculo do índice de auto-incompatibilidade (ISI) indicam que a espécie apresenta comportamento protogínico e é autocompatível, produzindo frutos em todos os tratamentos de autopolinização em proporções semelhantes à polinização natural, não sendo confirmada a produção de frutos apomíticos. Entretanto, os percentuais de frutos formados nos tratamentos de xenogamia foram significativamente superiores aos tratamentos de autofertilização, indicando que B. coccolobifolia apresenta um sistema reprodutivo misto com níveis elevados de alogamia e autogamia.

Estudios evolutivos en especies de plantas nativas.

Se indagará principalmente acerca del rol de los procesos neutrales, como la deriva génica, de procesos selectivos, como la selección natural mediada por polinizadores y de procesos históricos (geológicos y climáticos del pasado) en la diversificación floral tanto a escala microevolutiva como macroevolutiva. La heterogeneidad ambiental que se presenta en amplios rangos geográficos puede promover la diferenciación entre poblaciones debido a las diferencias en condiciones físicas y biológicas. De esta manera, especies ampliamente distribuidas ofrecen la oportunidad de explorar la dinámica de los procesos evolutivos que tienen lugar a nivel interpoblacional (Dobzhansky 1970, Thompson 1999). El estudio comparativo entre especies hermanas permite comprender cómo la selección natural (adaptación) y la inercia filogenética (herencia ancestral) han modelado los rasgos de las especies que observamos en la actualidad (Díaz 2002, Schluter 2000, Futuyma 2005). Uno de los usos más importantes de la información filogenética es el de reconstruir la historia del cambio evolutivo en caracteres adaptativos mediante su mapeo en la filogenia y la reconstrucción del estado de estos caracteres en el ancestro. Así, la asociación entre transición de caracteres y transiciones en grupos funcionales es una evidencia directa de la hipótesis adaptativa de que los rasgos son seleccionados por grupos funcionales de polinizadores. Una aproximación filogenética puede permitir identificar la dirección y el tiempo de evolución. Todos estos aspectos señalan la necesidad de adoptar una perspectiva conceptualmente integrada (morfológica, genética, filogenética, filogeográfica y ecológica) en el estudio de la biología evolutiva de las flores. Estudiar como actúan los procesos micro- y macroevolutivos en las interacciones planta-polinizador, en una dimensión espacial y temporal, arrojará resultados importantes tanto en el campo teórico como en el de la conservación. Por una parte, permitirá poner a prueba hipótesis relevantes sobre la adaptación de caracteres, mientras que explorará los procesos evolutivos que subyacen a las tramas de las interacciones planta-polinizador; por otro lado, comprender el rol de los cambios climáticos pasados en la diversificación biológica es interesante tanto desde una aproximación evolutiva como desde la biología de la conservación (Avise 2000; Moritz et al. 2000; Petit et al. 2003; Hewitt 2004). Géneros a ser estudiados en este proyecto: 1- Anarthrophyllum (Fabaceae,15 spp), 2- Monttea (Plantaginaceae, 3 spp), 3- Caleolaria (Calceolariaceae 3 spp), 4- Centris (Apidae, 1 spp), 5- Jaborosa (Solanaceae, 23 spp). Metodología: Mapeado de las poblaciones. Elenco de polinizadores, frecuencia. Obtención y medición de caracteres fenotípicos florales. Néctar: concentración y vol. Aceites (peso); Morfometría geométrica (Zelditch et al. 2005). Éxito reproductivo (Dafni & Kevan 2003). Caracteres genéticos: extracción, amplificación y secuenciación: en Calceolaria se utilizarán 2 genes de cloroplasto trnH-psbA y trnS-trnG y genes anónimos nucleares de copia única (scnADN), para Jaborosa se utilizarán 3 genes de cloroplasto (trnH-psbA, TrnD-trnT y ndhF-rp32) y el gen nuclear GBSSI waxy. Finalmente para Centris cineraria se usaría el tRNA ILE y NADH Deshidrogenada subunidad 2. Análisis filogenéticos de parsimonia (Goloboff et al. 2000, Kitching et al. 1998, Nixon 2002, Farris et al. 1996, Sorenson 1999); Filogeografía: reconstrucción de redes por parsimonia (Clement et al. 2000; Posada et al. 2000), análisis de clados anidados (NCPA). Se usarán las claves de inferencia (Templeton 2004). Para todos estos análisis se utilizarán los siguientes programas: DnaSP, Network, Arlequin, MrBayes, Paup, ModelTest, Beast, TNT, WinClada TCS y GeoDis. Estadística multivariada: Los diferentes rasgos florales mencionados se analizarán utilizando distancias de Gower (datos cualitativos) y euclídeas (datos cuantitativos) mediante la técnica multivariada ACoP.

Atividades relacionadas à construção e aprovisionamento de ninhos de Xylocopa subcyanea (Hymenoptera, Apidae) em uma área de restinga na Bahia, Brasil

As abelhas do gênero Xylocopa Latreille, 1802 são comuns em ecossistemas de restingas em acelerada fase de degradação e são importantes polinizadores deste ecossistema. Elas nidificam especialmente em madeira morta ou apodrecida. As atividades relacionadas à construção e estrutura dos ninhos de Xylocopa (Schoenherria) subcyanea Perez, 1901 na restinga do litoral norte da Bahia, Brasil, foram observadas em 43 ninhos ativos de X. subcyanea, em diferentes fases de desenvolvimento, em dois troncos apodrecidos. A fase de fundação ou reuso no primeiro tronco foi em agosto e a fase de provisionamento das células nos ninhos, em ambos troncos, em janeiro. As principais atividades foram escavações no tronco, entrada e saída dos ninhos, permanência na entrada do ninho, entrada com pólen e desidratação de néctar. Foi observado horário preferencial ao longo do dia para as atividades de entrada e saída dos ninhos, sendo estas influenciadas pelos horários do nascer e pôr do sol. Ninhos abandonados foram reusados por X. subcyanea e Centris tarsata SMITH, 1874. Os ninhos ativos eram ocupados por quatro diferentes abelhas adultas. Geralmente, uma abelha ficava na entrada do ninho. A estrutura do ninho foi descrita.

Revisão sistemática, análise cladística e biogeografia dos gêneros Tribotropis e Hypselotropis (Coleoptera, Anthribidae, Anthribinae, Ptychoderini)

Os gêneros Tribotropis Jekel, 1855 e Hypselotropis Jekel, 1855 são revisados. Com base nos resultados da análise cladística que incluiu 41caracteres e 22 táxons, o gênero Tribotropis é parafilético com relação a Hypselotropis, desta forma apresenta-se a proposta de sinonímia de Tribotropis syn. nov., sinônimo júnior. O gênero Hypselotropis, sinônimo sênior, e 17 espécies são redescritos, incluindo as espécies anteriormente alocadas em Tribotropis: Hypselotropis apollinaris (Jordan, 1939) comb. nov.; H. colombiana (Mermudes, 2004) comb. nov.; H. compressicornis (Jordan, 1895) comb. nov.; H. conicollis (Jekel, 1855) comb. nov.; H. limodes (Jordan, 1939) com. nov.; H. prasinata (Fahraeus, 1839) comb. nov.; H. punctulata (Jekel, 1855) comb. nov.; H. pustulata (Fabricius, 1801) comb. nov; H. speciosa (Jekel, 1855) comb. nov.; H. subvittata (Jordan, 1937) comb. nov.; H. suffusa (Jordan, 1895) comb. nov.; e H. vittata (Kirsch, 1889) comb. nov. Chave para identificação das espécies, ilustrações e mapas de distribuição são fornecidos. A biogeografia baseada nos padrões de distribuição das espécies é discutida.

Revisão taxonômica de Kanaima Distant (Hemiptera, Cercopidae, Ischnorhininae)

Kanaima Distant, 1909 é revisado, sendo suas espécies descritas e redefinidas. Este trabalho ressalta os caracteres taxonomicamente importantes das espécies de Kanaima, como os da morfologia externa e da genitália. Quatro espécies são reconhecidas como válidas: K. katzensteinii (Berg, 1879), K. fluvialis (Lallemand, 1924), K. fusca (Lallemand, 1927) comb. nov., e K. nigra sp. nov. (Brasil, RS). Os nomes Monecphora fluvialis var. lateralis Lallemand, 1924 e Monecphora fluvialis var. bipunctata Lallemand, 1924 são sinonimizados sob Kanaima fluvialis. Quatro espécies incluídas em Kanaima são transferidas para Mahanarva: M. (Ipiranga) vittata (Walker, 1851) comb. nov., M. (Ipiranga) fortunata (Lallemand, 1924) comb. nov., M. (Mahanarva) radiata (Walker, 1851) comb. nov. e M. (Mahanarva) dubia (Stancik & Cavichioli, 2003) comb. nov. Pachypterinella Lallemand, 1927 sin. nov.

Two new Neotropical species of the genus Oxysarcodexia Townsend (Diptera, Sarcophagidae)

Two new Neotropical species of the genus Oxysarcodexia Townsend (Diptera, Sarcophagidae). Oxysarcodexia nitida sp. nov. and O. notata sp. nov. from Peru are described and illustrated based on male specimens. These new taxa are morphologically more similar to O. vittata (Walker) and O. xon (Dodge) respectively.