Spodosols pedogenesis under barreiras formation and sandbank environments in the south of Bahia

Morphologically differentiated Spodosols usually occur in the Coastal Plain of the South of Bahia and North of Espírito Santo. They are found in profiles known as "muçungas", i.e. sandy soils that accumulate water. In these areas, two kinds of Spodosols, different from those in the Restinga area, can be found: Spodosols with E albic horizon (white muçunungas) and without this horizon (black muçunungas). Eight soil profiles with spodic characteristics were collected and described in order to evaluate differences in the formation process of Barreiras and Restinga Spodosols in the South of Bahia. The soil profiles were also characterized chemically, physically and mineralogically. Additionally, texture and chemical analysis, Fe and Al extraction by sodium dithionite-citrate-bicarbonate (DBC), acid ammonium oxalate and sodium pyrophosphate, ammonium oxalate extract optic density (DOox), sulphuric acid attack, and X ray difractometry of the clay fraction were performed. In the Spodosols of the Barreiras area, fragipan was found the spodic layers. Cemented B spodic horizon were observed in the white muçunungas, and granular structure and dark color from the surface in the black muçunungas. There was no fragipan or hard spodic horizon in the Restinga Spodosol. This soil is acid, dystrophic and alic, with sandy texture and high clay percentages in the spodic horizons. The CEC, based on H + Al, is predominantly represented by the organic matter. The most representative components of the mineral phase of the clay fraction are kaolinite and possibly vermiculite traces with interlayered hydroxy. Chemical, physical, morphological and mineralogical differences were observed between the Barreiras and Restinga environments. The black and white muçunungas differ in morphologic and chemical properties only.

Comportamento de superfosfato simples contendo fosfato de ferro de baixa solubilidade em água em solos de várzea do Rio Grande do Sul

Algumas rochas utilizadas na produção de fertilizantes contêm impurezas de baixa solubilidade em água, destacando-se alguns fosfatos de Fe e Al, que poderiam ser aplicados em solos alagados, onde as reações de redução podem aumentar a solubilidade. O objetivo deste trabalho foi estudar a liberação do P de fertilizantes contendo impurezas de fosfatos de Fe com baixa solubilidade em água em diferentes solos de várzea do Rio Grande do Sul (RS) sob condições de alagamento. Para realização do experimento foram utilizados seis solos de várzea (dois Gleisssolos, dois Planossolos e dois Chernossolos) de diferentes locais do Estado do Rio Grande do Sul, os quais foram acondicionados em vasos plásticos de 8 L. Cada solo recebeu duas fontes de P (superfosfato simples e superfosfato simples com resíduos de Fe) e uma testemunha sem adição de P, com três repetições. Nos tratamentos com P foram adicionados ao solo 100 mg kg-1 P no solo. Os solos foram alagados e mantidos, em delineamento inteiramente casualizado e três repetições, com uma lâmina de água de 5 cm de altura acima de sua superfície. A solução do solo foi coletada semanalmente, sendo medidos imediatamente o pH e o potencial redox (Eh); posteriormente, procedeu-se, em laboratório, à determinação dos teores de P e Fe. Os resultados mostram redução do Eh e aumento do pH e dos teores de Fe e P em solução para todos os solos. O teor de P na solução não diferiu quanto à fonte, mostrando que o superfosfato simples com impurezas de fosfato de Fe tem potencial de uso em solos de várzea do Rio Grande do Sul cultivados com arroz irrigado por alagamento, mesmo sem a solubilidade em água prevista na legislação brasileira.

Variabilidade espacial de atributos mineralógicos de solos da formação Guabirotuba, Curitiba (PR)

As características físicas e químicas do solo são fortemente influenciadas pela sua constituição mineralógica, as quais, mesmo a curtas distâncias horizontais, podem apresentar alta variabilidade espacial, fato que pode ser descrito mais adequadamente pela associação entre a estatística descritiva clássica e a geoestatística. O objetivo deste trabalho foi caracterizar a variabilidade espacial de atributos mineralógicos da fração argila de solos da Formação Guabirotuba, região metropolitana de Curitiba (PR), por meio da estatística clássica descritiva (em especial o CV) e da geoestatística como forma de indicar melhores padrões de amostragem para esses atributos. As amostras do horizonte B foram coletadas na interseção de uma malha georreferenciada com espaçamento regular a 30 m, adicionando-se mais 10 % de pontos com posicionamento aleatório para reduzir o efeito-pepita (total de 135 amostras). Para a descrição da dispersão e variabilidade dos dados foi utilizada a análise por estatística descritiva clássica (média, mediana, máximo, mínimo, desvio-padrão, coeficiente de variação (CV), assimetria, curtose e teste de Shapiro-Wilk), enquanto para a caracterização da variabilidade espacial utilizou-se a geoestatística na produção dos semivariogramas. Os teores de caulinita (Ct) apresentaram baixo CV (10,8 %), porém alta variabilidade espacial, com alcance de apenas 22,4 m. Já o atributo que apresentou maior CV foi a relação Fe amorfo/Fe cristalino (94,6 %), indicando grande dispersão dos valores em relação à média, no entanto seu alcance foi de 64,6 m, evidenciando média a baixa variabilidade espacial. Foi observado efeito-pepita puro apenas na substituição isomórfica de Fe por Al na hematita (Hm). O Fe cristalino foi o atributo que apresentou maior alcance, com valor de 625 m. Contudo, quando se analisaram os teores de Hm e goethita separadamente, a variabilidade espacial foi ampliada.

Podzolização em solos de áreas de depressão de topo dos tabuleiros costeiros do Nordeste brasileiro

Os solos associados às depressões de topo dos Tabuleiros Costeiros são diferenciados sob vários aspectos ainda pouco estudados no Brasil. Geralmente, à medida que se aproxima dessas depressões, nota-se que a textura dos solos é mais arenosa e o hidromorfismo, mais acentuado, sendo comum a ocorrência de Espodossolos. Neste contexto, o objetivo deste trabalho foi realizar diferentes extrações de Fe, Al, Si e C orgânico com o intuito de compreender o processo de podzolização em solos associados às depressões de topo dos Tabuleiros Costeiros do Nordeste brasileiro. Foram descritos perfis e coletadas amostras de solo em quatro áreas: Coruripe, AL; Neópolis, SE; Acajutiba, BA; e Nova Viçosa, BA. Nas amostras, determinou-se o teor de Fe, Al e Si pelos extratores ditionito-citrato-bicarbonato de sódio, oxalato de amônio e pirofosfato de sódio e realizou-se o fracionamento químico da matéria orgânica do solo. Os aumentos nos teores de C orgânico e de Fe e Al pelos diferentes extratores nos horizontes iluviais (de acúmulo) de cada solo, relativamente aos horizontes eluviais (de perda), refletiram a morfologia de campo e reforçaram a importância do processo de podzolização nos solos estudados. Complexos Al-húmus dominam inteiramente a matriz dos horizontes iluviais associados ao hidromorfismo, enquanto naqueles sem hidromorfismo a influência das diferentes formas de Fe é variável. O perfil de Espodossolo Ferrihumilúvico é o único, dos quatro estudados, que possui horizontes espódicos com subscrito "s" e, portanto, onde os teores de Fe extraídos refletiram-se diferencialmente na morfologia.

Lead and zinc in the structure of organic and mineral soil components

In addition to the more reactive forms, metals can occur in the structure of minerals, and the sum of all these forms defines their total contents in different soil fractions. The isomorphic substitution of heavy metals for example alters the dimensions of the unit cell and mineral size. This study proposed a method of chemical fractionation of heavy metals, using more powerful extraction methods, to remove the organic and different mineral phases completely. Soil samples were taken from eight soil profiles (0-10, 10-20 and 20-40 cm) in a Pb mining and metallurgy area in Adrianópolis, Paraná, Brazil. The Pb and Zn concentrations were determined in the following fractions (complete phase removal in each sequential extraction): exchangeable; carbonates; organic matter; amorphous and crystalline Fe oxides; Al oxide, amorphous aluminosilicates and kaolinite; and residual fractions. The complete removal of organic matter and mineral phases in sequential extractions resulted in low participation of residual forms of Pb and Zn in the total concentrations of these metals in the soils: there was lower association of metals with primary and 2:1 minerals and refractory oxides. The powerful methods used here allow an identification of the complete metal-mineral associations, such as the occurrence of Pb and Zn in the structure of the minerals. The higher incidence of Zn than Pb in the structure of Fe oxides, due to isomorphic substitution, was attributed to a smaller difference between the ionic radius of Zn2+ and Fe3+.

Chemical properties and mineralogy of soils with plinthite and petroplinthite in Iranduba (AM), Brazil

Large areas of Plinthosols with ferruginous materials such as plinthite and/or petroplinthite are fairly common in the Brazilian Amazon basin. This work was carried out to investigate the chemical behavior, mineralogical composition and weathering stage of four representative soil profiles with plinthite and petroplinthite, in Iranduba, AM (Central Amazon). Three well-drained soil profiles at high elevations were studied (P1, Plinthic Vetic Ferralsol; P2 and P3, Vetic Endopetric Plinthosol) and a contrasting poorly drained soil (P4 Haplic Plinthosol), located at low elevation. After profile descriptions, soil samples were collected from each horizon, air-dried, sieved (2 mm), and analyzed for particle-size distribution, pH, exchangeable cations (Al3+, Ca2+, Mg2+, K+, and Na+), as well as available P and total organic carbon (TOC) content. The minerals present in the clay and sand fractions, as well as in the ferruginous materials were identified by X-ray Diffraction (XRD). The weathering stage of these soils was assessed by means of Ki and Kr indexes, and the amounts of free and amorphous Fe and Al oxides by using dithionite citrate bicarbonate (DBC) and ammonium oxalate dissolution procedures, respectively. The results showed that all soils were extremely unfertile, with pH levels ranging between strong and moderate acidity, very low sum of bases and organic matter content, and of available P. The mineralogy of the soil profiles was very similar, mainly of the well-drained soils, with predominance of kaolinite and quartz in the clay and sand fractions, respectively. In the poorly-drained P4, 2:1 clay particles were also observed. These profiles can be considered highly developed according to the Ki index, however, the Ki value of P4 was higher, indicating that this soil was less developed than the others. In summary, these profiles with plinthite and petroplinthite can be characterized as highly developed and infertile soils and are, with exception of P4, well-drained.

Reserva mineral de potássio em Latossolo cultivado com Pinus taeda L.

No Brasil, aproximadamente 1,87 milhões de hectares são plantados com as espécies de Pinus, normalmente em solos pobres quimicamente. Os objetivos deste trabalho foram estudar a mineralogia das frações areia, silte e argila e estimar a reserva mineral de K por diferentes métodos de extrações químicas em solo naturalmente pobre nesse nutriente e cultivado com Pinus taeda L., no Segundo Planalto Paranaense. Foram selecionadas cinco árvores com maior diâmetro (árvores dominantes), em uma área de 500 m², para abertura de uma trincheira (1,6 m) na projeção da copa de cada árvore. Todos os perfis foram classificados como Latossolo Vermelho-Amarelo distrófico típico e apresentaram similaridade na morfologia e na sequência dos horizontes, cujas profundidades médias foram: O = 0,04 m, A1 = 0-0,09 m, A2 = 0,09-0,24 m, BA = 0,24-0,43 m, B1 = 0,43-0,66 m e B2 = 0,66-1,60+ m. As amostras coletadas em cada horizonte foram submetidas a análises físicas (granulometria) e químicas (pH, carbono orgânico, acidez potencial, Al3+ e bases trocáveis, P disponível, K total e não trocável), e as frações areia, silte e argila foram estudadas por difratometria de raios-X (DRX). As frações areia e silte dos solos apresentaram mineralogia bastante uniforme, com predomínio absoluto de quartzo e apenas ocorrência de discretas reflexões de mica por DRX. A fração argila também apresentou limitada ocorrência de minerais micáceos. Os tratamentos sequenciais para remoção de óxidos de Fe, gibbsita e caulinita foram eficientes para concentração de mica na fração argila, o que facilitou a identificação de biotita e muscovita por DRX. Os baixos teores de K não trocável obtidos com diferentes concentrações de HNO3 fervente (máximo de 91 mg kg-1) e de K total extraído com HF concentrado (máximo de 202,7 mg kg-1) foram consistentes com a pobreza das frações do solo em minerais primários, fontes desse nutriente. As correlações positivas e significativas entre os teores não trocáveis de K no solo e os teores e conteúdos do nutriente nas árvores indicaram a importância de formas de reservas do nutriente na nutrição da espécie em solos altamente intemperizados e pobres em K trocável.

Paragênese mineral de solos desenvolvidos de diferentes litologias na região sul de Minas Gerais

Estudos sistemáticos sobre os fatores de formação do solo são relativamente escassos no Brasil, em razão da dificuldade de amostrar vários níveis de um fator, mantendo os demais constantes. A região de Lavras, MG, possui grande diversidade geológica em uma área pequena, o que possibilita avaliar o controle exercido por diferentes litologias na mineralogia e nas demais características do solo. Foram selecionados oito solos embasados sobre quartzito, mica-xisto, gabro, itabirito, serpentinito, metacalcário, gnaisse e filito, em condições semelhantes de vegetação (floresta tropical semidecidual), relevo (terço médio de encosta) e clima. Após a descrição dos perfis, coletaram-se amostras dos horizontes e das rochas, e realizaram-se análises físicas e químicas de rotina, composição química total e mineralogia da rocha, da areia e da argila do solo. Todos os solos são pobres em bases trocáveis (exceto o Argissolo sobre itabirito), e notou-se grande variação na composição granulométrica, mineralógica e química. Os teores de Al2O3, SiO2 e Fe2O3 presentes nas rochas não evidenciaram correlação com os respectivos teores nos solos derivados, enquanto o teor de Fe2O3 foi fortemente correlacionado à densidade de partículas e suscetibilidade magnética. Apesar de evidências de material parcialmente alóctone em alguns casos, pôde-se notar forte influência da litologia subjacente na paragênese mineralógica. Os solos foram genericamente agrupados em: cauliníticos com minerais 2:1 (Argissolos sobre mica-xisto e itabirito; e Cambissolo sobre quartzito), cauliníticos (Argissolos sobre gnaisse e filito) e oxídicos (Latossolos sobre metacalcário e gabro; e Plintossolo sobre serpentinito). Os processos de monossialitização e alitização predominam na região, sendo respectivamente associados a rochas com valores intermediários e baixos em sílica, enquanto a presença de minerais 2:1 é acessória à caulinita e parece depender da presença de mica e altos teores de sílica na rocha de origem.

Chemical and mineralogical changes in a Brazilian Rhodic Paleudult under different land use and managements

Changes in land use and management can affect the dynamic equilibrium of soil systems and induce chemical and mineralogical alterations. This study was based on two long-term experiments (10 and 27 years) to evaluate soil used for no-tillage maize cultivation, with and without poultry litter application (NTPL and NTM), and with grazed native pasture fertilized with cattle droppings (GrP), on the chemical and mineralogical characteristics of a Rhodic Paleudult in Southern Brazil, in comparison with the same soil under native grassland (NGr). In the four treatments, soil was sampled from the 0.0-2.5 and 2.5-5.0 cm layers. In the air-dried fine soil (ADFS) fraction (∅ < 2 mm), chemical characteristics of solid and liquid phases and the specific surface area (SSA) were evaluated. The clay fraction (∅ < 0.002 mm) in the 0.0-2.5 cm layer was analyzed by X-ray diffraction (XRD) after treatments for identification and characterization of 2:1 clay minerals. Animal waste application increased the total organic C concentration (COT) and specific surface area (SSA) in the 0.0-2.5 cm layer. In comparison to NGr, poultry litter application (NTPL) increased the concentrations of Ca and CECpH7, while cattle droppings (GrP) increased the P and K concentrations. In the soil solution, the concentration of dissolved organic C was positively related with COT levels. With regard to NGr, the soil use with crops (NTM and NTPL) had practically no effect on the chemical elements in solution. On the other hand, the concentrations of most chemical elements in solution were higher in GrP, especially of Fe, Al and Si. The Fe and Al concentrations in the soil iron oxides were lower, indicating reductive/complexive dissolution of crystalline forms. The X-ray diffraction (XRD) patterns of clay in the GrP environment showed a decrease in intensity and reflection area of the 2:1 clay minerals. This fact, along with the intensified Al and Si activity in soil solution indicate dissolution of clay minerals in soil under cattle-grazed pasture fertilized with animal droppings.

Geoquímica de solos do pantanal norte, Mato Grosso

A caracterização e análise geoquímica de solos permitem compreender os processos de migração, dispersão e concentração de elementos químicos no perfil, embasando a correlação dos atributos deles com as classes de solos formadas, o que possibilita inferências acerca das gêneses desses solos. Esta pesquisa teve por objetivos caracterizar e interpretar a composição geoquímica total de elementos maiores e menores em classes de solos representativas do Pantanal norte, na sub-região de Barão de Melgaço, Mato Grosso, Brasil. Foram selecionados 20 perfis das principais classes de solos do Pantanal e analisadas amostras dos horizontes A e B (ou C) quanto à concentração de óxidos totais por espectrometria de fluorescência de raios-X, além das caracterizações física, química e mineralógica. Os solos subdividiram-se em dois tipos geoquímicos: um composto por textura arenosa a franco-arenosa com teores relativamente elevados de SiO2 e predominância de caulinita e quartzo, com menor teor de bases e elementos-traço; e outro composto por textura mais argilosa, geoquimicamente heterogêneos e com teores significativos de minerais 2:1, Al2O3, óxidos de Fe e Mn, bases e elementos-traço.

Cover plants and mineral nitrogen: effects on organic matter fractions in an oxisol under no-tillage in the cerrado

Cover plants are essential for the sustainability of no-tillage systems in tropical regions. However, information on the effects of these plants and N fertilization on soil organic matter fractions is still scarce. This study evaluated the effect of cover crops with different chemical composition and of N topdressing on the labile and humified organic matter fractions of an Oxisol of the Cerrado (savanna-like vegetation). The study in a randomized complete block design was arranged in split-plots with three replications. Four cover species were tested in the plots and the presence or absence of N topdressing in the subplot. The following cover species were planted in succession to corn for eight years: Urochloa ruziziensis; Canavalia brasiliensis M. ex Benth; Cajanus cajan (L.) Millsp; and Sorghum bicolor (L.) Moench. In general, the cultivation of U. ruziziensis increased soil C levels, particularly of C in the humic acid and particulate organic C fractions, which are quality indicators of soil organic matter. The C in humic substances and mineral organic C accounted for the highest proportions of total organic C, demonstrating the strong interaction between organic matter, Fe and Al oxides and kaolinite, which are predominant in these weathered soils of the Cerrado.

Influência da Matéria Orgânica no Diâmetro Médio de Minerais da Fração Argila de Solos Desenvolvidos de Basalto no Sul do Brasil

RESUMO A interação de compostos orgânicos com minerais de argila pode alterar o tamanho dos cristais. No entanto, em solos, esse efeito é ainda pouco claro por causa das limitações na separação de fases puras de minerais para realizar experimentos de dissolução. Neste estudo, a relação entre a matéria orgânica do solo (MOS) e diâmetro médio do cristal (DMC) de minerais de argila de horizontes superficiais e subsuperfíciais de solos de uma topossequência no sul do Brasil foi avaliada. Os teores de C e N foram determinados, e a natureza dos grupos funcionais da MOS foi avaliada por espectroscopia de FTIR. O DMC dos minerais foi avaliado por difração de raios X, em umas amostras desferrificadas e outras com óxidos de Fe concentrados. Os teores de C e N e as intensidades relativas dos espectros de FTIR foram considerados como variáveis preditoras; e o DMC de hematita, goethita, caulinita e gibbsita, como variáveis preditas. Os teores de C e N e os grupos carboxílicos e C-O-Alquil evidenciaram efeito significativo sobre a variação do DMC. A dimensão dos cristais de óxidos de Fe e de caulinita foi inversamente correlacionada com esses atributos da MOS. Em contraste, o DMC de gibbsita não foi influenciado pelos atributos dae MOS. A influência da MOS sobre o DMC dos óxidos de Fe foi atribuída às reações de complexação de superfície e de redox, que promovem um processo contínuo de dissolução-precipitação.

Long-term and long range migration of radioisotopes in terrestrial systems : mechanisms of radioisotopes (Cs, Sr, Pu, Am) mobilization in soils

Summary Artificial radionuclides were released in the environment during the atmospheric nuclear weapon tests and after accidental events involving nuclear industries. As a primary receptor of the deposition, the soil is a very sensitive compartment and understanding the interaction and migration of radionuclides within soils allows the development of scenario for the contamination risk of the population and of the environment. Most available field studies on radionuclides in soils only concern one or two isotopes, mostly 137Cs, and few physico-chemical soil parameters. The purpose of this study was a broader understanding of the radioecology of an Alpine valley. In a first part, we aimed to describe the depth distribution of 137Cs, 90Sr, 239+240Pu, and 241Am within different alpine soils and to identify some stable elements as indicators for accumulating layers. In the central part of the study, the goal was to investigate the repartition of ^Sr and 239Pu between the truly dissolved fraction and the colloidal fraction of the soil solutions and to identify the nature of colloids involved in the adsorption of ^Sr and 239Pu. These results were integrated in an "advection- sorption" transport model seeking to explain the migration of 239Pu and 90Sr within the soils and to assess the importance of colloidal transport for these two isotopes. A further aspect studied was the role of the competition between the radioisotopes (137Cs and 90Sr) and their stable chemical analogues (K and Ca) with respect to plant uptake by different plant species. The results on the depth distribution within the soils showed that 137Cs was mostly retained in the topsoil, to the exception of an organic-rich soil (Histosol 2) receiving important surface runoff, where migration down to a depth of 30 cm was observed. 137Cs depth distribution within the soils was similar to unsupported 210Pb depth distribution. The plant uptake of 137Cs clearly depended on the concentration of exchangeable potassium in the soils. Moreover, we showed that the 137Cs uptake by certain species of the taxonomic orders Poales and Rosales was more sensitive to the increase in exchangeable Κ compared to other orders. Strontium-90 was much more mobile in the soils than 137Cs and depth migration and accumulation in specific AI- and Fe-rich layers were found down to 30 cm. Copper and Ni showed accumulations in these same layers, indicating their potential to be used as indicators for the migration of ^Sr within the soils. In addition, we observed a 90Sr activity peak in the topsoil that can be attributable to recycling of 90Sr by plant uptake. We demonstrated for the first time that a part of 90Sr (at least 40%) was associated with the colloids in organic-rich soil solutions. Therefore, we predict a significant effect of the colloidal migration of ^Sr in organic-rich soil solutions. The plant uptake results for 90Sr indicated a phylogenetic effect between Non-Eudicot and Eudicots: the order Poales concentrating much less 90Sr than Eudicots do. Moreover, we were able to demonstrate that the sensitivity of the 90Sr uptake by 5 different Alpine plant species to the amount of exchangeable Ca was species-independent. Plutonium and 241Am accumulated in the second layer of all soils and only a slight migration deeper than 20 cm was observed. Plutonium and 241Am showed a similar depth distribution in the soils. The model results suggested that the present day migration of 239Pu was very slow and that the uptake by plants was negligible. 239Pu activities between 0.01 to 0.08 mBq/L were measured in the bulk soil solutions. Migration of 239Pu with the soil solution is dominated by colloidal transport. We reported strong evidences that humic substances were responsible of the sorption of 239Pu to the colloidal fraction of the soil solutions. This was reflected by the strong correlation between 239Pu concentrations and the content of (colloidal) organic matter in the soil solution. Résumé Certains radioéléments artificiels ont été disséminés dans l'environnement suite aux essais atmosphériques de bombes nucléaires et suite à des accidents impliquant les industries nucléaires. En tant que récepteur primaire de la déposition, le sol est un compartiment sensible et des connaissances sur les interactions et la migration des radioéléments dans le sol permettent de développer des modèles pour estimer la contamination de la population et de l'environnement. Actuellement, la plupart des études de terrain sur ce sujet concernent uniquement un ou deux radioéléments, surtout le 137Cs et peu d'études intègrent les paramètres du sol pour expliquer la migration des radioéléments. Le but général de cette étude était une compréhension étendue de la radio-écologie d'une vallée alpine. Notre premier objectif était de décrire la distribution en profondeur de 137Cs, ^Sr, 239+240pu et 241Am dans différents sols alpins en relation avec des éléments stables du sol, dans le but d'identifier des éléments stables qui pourraient servir d'indicateurs pour des horizons accumulateurs. L'objectif de la deuxième partie, qui était la partie centrale de l'étude, était d'estimer le pourcentage d'activité sous forme colloïdale du 239Pu et du 90Sr dans les solutions des sols. De plus nous avons déterminé la nature des colloïdes impliqués dans la fixation du ^Sr et 239Pu. Nous avons ensuite intégré ces résultats dans un modèle de transport développé dans le but de décrire la migration du 239Pu et 90Sr dans le sol. Finalement, nous avons étudié l'absorption de 137Cs et 90Sr par les plantes en fonction de l'espèce et de la compétition avec leur élément analogue stable (K et Ca). Les résultats sur la migration en profondeur du 137Cs ont montré que ce radioélément était généralement retenu en surface, à l'exception d'un sol riche en matière organique dans lequel nous avons observé une nette migration en profondeur. Dans tous les sols, la distribution en profondeur du 137Cs était corrélée avec la distribution du 210Pb. L'absorption du 137Cs par les plantes, était dépendante de la concentration en Κ échangeable dans le sol, le potassium étant un compétiteur. De plus, nous avons observé que les espèces ne réagissaient pas de la même manière aux variations de la concentration de Κ échangeable. En effet, les espèces appartenant aux ordres des Poales et des Rosales étaient plus sensibles aux variations de potassium échangeable dans le sol. Dans tous les sols Le 90Sr était beaucoup plus mobile que le 137Cs. En effet, nous avons observé des accumulations de 90Sr dans des horizons riches en Fe et Al jusqu'à 30 cm de profondeur. De plus, le Cu et le Ni montraient des accumulations dans les mêmes horizons que le 90Sr, indiquant qu'il pourrait être possible d'utiliser ces deux éléments comme analogues pour la migration du 90Sr. D'après le modèle développé, le pic de 90Sr dans les premiers centimètres du sol peut être attribué à du recyclage par les plantes. Le 90Sr en solution était principalement sous forme dissoute dans des solutions de sols peu organique (entre 60 et 100% de 90Sr dissous). Par contre, dans des solutions organiques, un important pourcentage de 90Sr (plus de 40%) était associé aux colloïdes. La migration colloïdale du 90Sr peut donc être significative dans des solutions organiques. Comme pour le 137Cs, l'absorption du 90Sr par les plantes dépendait de la concentration de son analogue chimique dans la fraction échangeable du sol. Par contre, les espèces de plantes étudiées avaient la même sensibilité aux variations de la concentration du calcium échangeable. Le plutonium et l'américium étaient accumulés dans le deuxième horizon du sol et nous avons observé seulement une faible migration plus profondément que 20 cm. Selon le modèle, la migration actuelle du plutonium est très lente et l'absorption par les plantes semble négligeable. Nous avons mesuré entre 0.01 et 0.08 mBq/L de 239Pu dans les solutions de sol brutes. La migration du plutonium par la solution du sol est due principalement aux colloïdes, probablement de nature humique. Résumé grand public Dans les années 1950 à 1960, l'environnement a été contaminé par des éléments radioactifs (radioéléments) artificiels provenant des essais des armes atomiques et de l'industrie nucléaire. En effet, durant ces années, les premiers essais de bombes atomiques se faisaient dans l'atmosphère, libérant de grandes quantités d'éléments radioactifs. De plus certains accidents impliquant l'industrie nucléaire civile ont contribué à la dissémination d'éléments radioactifs dans l'environnement. Ce fut par exemple le cas de l'accident de la centrale atomique de Tchernobyl en 1986 qui a causé une importante contamination d'une grande partie de l'Europe par le 137Cs. Lorsqu'ils sont libérés dans l'atmosphère, les radioéléments sont dispersés et transportés par les courants atmosphériques, puis peuvent être déposés dans l'environnement, principalement par les précipitations. Une fois déposés sur le sol, les radioéléments vont interagir avec les composants du sol et migrer plus ou moins vite. La connaissance des interactions des éléments radioactifs avec le sol est donc importante pour prédire les risques de contamination de l'environnement et de l'homme. Le but général de ce travail était d'évaluer la migration de différents éléments radioactifs (césium-137, strontium-90, plutonium et américium-241) à travers le sol. Nous avons choisi un site d'étude en milieu alpin (Val Piora, Tessin, Suisse), contaminé en radioéléments principalement par les retombées de l'accident de Tchernobyl et des essais atmosphériques de bombes atomiques. Dans un premier temps, nous avons caractérisé la distribution en profondeur des éléments radioactifs dans le sol et l'avons comparée à divers éléments stables. Cette comparaison nous a permit de remarquer que le cuivre et le nickel s'accumulaient dans les mêmes horizons du sol que le strontium-90 et pourraient donc être utilisés comme analogue pour la migration du strontium-90 dans les sols. Dans la plupart des sols étudiés, la migration du césium-137, du plutonium et de l'américium-241 était lente et ces radioéléments étaient donc accumulés dans les premiers centimètres du sol. Par contre, le strontium-90 a migré beaucoup plus rapidement que les autres radioéléments si bien qu'on observe des accumulations de strontium-90 à plus de 30 cm de profondeur. Les radioéléments migrent dans la solution du sol soit sous forme dissoute, soit sous forme colloïdale, c'est-à-dire associés à des particules de diamètre < Ιμηι. Cette association avec des colloïdes permet à des radioéléments peu solubles, comme le plutonium, de migrer plus rapidement qu'attendu. Nous avons voulu savoir quelle était la part de strontium-90 et plutonium associés à des colloïdes dans la solution du sol. Les résultats ont montré que le plutonium en solution était principalement associé à des colloïdes de type organique. Quant au strontium-90, ce dernier était en partie associé à des colloïdes dans des solutions de sol riches en matière organique, par contre, il était principalement sous forme dissoute dans les solutions de sol peu organiques. L'absorption de radioéléments par les plantes représente une voie importante pour le transfert vers la chaîne alimentaire, par conséquent pour la contamination de l'homme. Nous avons donc étudié le transfert du césium-137 et du strontium-90 de plusieurs sols vers différentes espèces de plantes. Les résultats ont montré que l'absorption des radioéléments par les plantes était liée à la concentration de leur analogue chimique (calcium pour le strontium-90 et potassium pour le césium- 137) dans la fraction échangeable du sol. De plus certaines espèces de plantes accumulent significativement moins de strontium-90.

Pollution trends using bark of morus alba in the cities of buenos aires and mendoza (Argentina)

A comparative study of elements deposited on tree bark was carried out for urban and periurban areas of two of the most important cities in Argentina. The content of Fe, Mg, Al, Mn, Zn, Pb, Ba, Cr, Hg, Cu, Ni, Cd and Sb was determined by inductively coupled plasma atomic emission spectrometry (ICP-OES) in Morus alba tree bark collected in the cities of Buenos Aires and Mendoza. The main air pollutants detected in the Buenos Aires urban area were Ba, Cr, Cu and Ni and indicate significative difference from the Mendoza urban and periurban areas. Significantly, higher concentrations of Zn, Ba, Cr and Cu were recorded in the periurban area of the city of Buenos Aires than in Mendoza. Bark samples were strongly influenced by dust and show Al, Fe, Mg and other element accumulations that indicate that soil particles were carried out by wind. Elements like Ba and Zn, commonly linked to traffic emissions, showed the highest concentrations in the Buenos Aires metropolitan area, possibly due to more intensive vehicular traffic. Our results indicated that intensity of vehicular traffic and not city structure is responsible for air pollution.

Interaction between the mineral content and the occurrence number of aquatic fungi in leaves submerged in a stream in the Atlantic rainforest, São Paulo, Brazil

Leaves of Ficus microcarpa L. f., Quercus robur L., and Alchornea triplinervia (Spreng.) Muell. Arg., submerged in a stream of the Atlantic rainforest in the "Reserva Biológica do Alto da Serra de Paranapiacaba", State of São Paulo, Brazil, were collected monthly, from April to November 1990, in order to determine the number of fungal occurrences (zoosporic fungi and aquatic Hyphomycetes), and the content of total N (%), total P (%), K+ (%), Ca+2 (%), Mg+2 (%), S+3 (%), Fe+3 (ppm), Cu+3 (ppm), Mn+2 (ppm), Zn+2 (ppm), Bo (ppm), Na+2 (ppm) and Al+3 (ppm). According to the tests of Kruskal-Wallis, Mann-Whitney and Wilcoxon, the means of the mineral content of the three types of leaves were significantly different, except for Mg+2 (%), Mn+2 (ppm), Zn+2 (ppm) and Na+2 (ppm). On comparing the mineral content with the number of fungal occurrence, an independence test showed a positive correlation between the presence of zoosporic fungi on the leaves of A. triplinervia and the total nitrogen, phosphorus and S+3 content, whereas the aquatic Hyphomycetes depended on the amount of Ca+2 available. Regarding leaves of F. microcarpa, the occurrence of zoosporic fungi was linked to the S+3 level, and the presence of aquatic Hyphomycetes, to the content of K+, Ca+2, S+3 and Bo. On Q. robur leaves, zoosporic fungi showed a positive correlation with the Ca+2 content, but a negative one with Fe+3 and Al+3 levels, while the occurrence of aquatic Hyphomycetes was influenced by the content of Ca+2, Mg+2, Fe+3, Al+3, Mn+2, Zn+2 and Na+2. The correlation between the occurrence number of aquatic Hyphomycetes and a high mineral content indicates that their nutritional requirements may be more complex than those of zoosporic fungi. Further studies are still required to understand the implications of this tendency on the diversity of aquatic native mycota.