Abstract: The aim of this study is to discuss the concentration distribution, composition and possible sources of trace metals and 13 PAHs in topsoils of the University campus, in the city of São Paulo, the largest city of South America. Mineralogy and granulometry of topsoils (0-10 cm) samples, were determined and As, Ba, Cd, Co, Cr, Cu, Mo, Ni, Pb, Sb, V, Zn, Hg, Pt, Pd and PAHs concentrations were quantified in the bulk fraction. The average clay content of soils was 221±61.8 g kg-1 and total carbon was low (mean of 25 g kg-1). Concentrations of metals were generally lower than the reference value established by the São Paulo State Environmental Agency and other studies in the São Paulo urban area, except for Cd, Ni, Pb, Cr and Zn. The mean concentration of the sum of 13 PAHs was 0.33 mg kg-1 and fluorene, indeno(1,2,3-cd)pyrene, anthracene, pyrene and benzo(ghi)perylene were the most abundant compounds. PAHs and trace metals variability were constrained in PMF analysis and showed an association with exhaust and non-exhaust vehicular emissions. The results also pointed out a spatial pattern in the campus area related to traffic conditions and intensity and terrain slope.

Abstract: The reviewed and integrated geoheritage inventory of the northern coast of the state of São Paulo, Brazil, resulted in 43 geosites distributed in eight geological frameworks. The selected geosites are representative of a geological history from the Neoproterozoic (Brasiliano-Pan African Cycle) to the recent, covering a minimum 700-Ma timespan. Considering the dynamic character of geoheritage inventories, the results presented in this work were based on previous local, town-based surveys, which were reviewed under the light of new geological data and geoconservation methods. Both qualitative and quantitative geosites assessments were used to discuss their geological representativeness and relevance, as well as legal aspects regarding protection and perspectives for future use. This resulted in a detailed inventory that reflects the current geological knowledge in the northern coast of the state of São Paulo, and may be used to make a general diagnosis of the scientific value, state of conservation, risk of degradation and potential use of the geoheritage. Moreover, it reinforces the importance of locally- and regionally-relevant sites for sustainable land management using geoheritage and to direct the decisions related to the conservation and use of this abiotic part of nature in the region.

Este trabalho teve como objetivo a caracterização e a comparação da composição química da fração solúvel do PM10, com variáveis meteorológicas, tais como, direção do vento e trajetórias de massas de ar. O PM10 foi coletado durante o inverno de 1999 em dois locais contrastantes: na cidade de São Paulo e no Parque Estadual da Serra do Mar (Cunha), Reserva de Mata Atlântica. Os extratos aquosos do PM10 foram analisados por Cromatografia de Íons para quantificação dos íons maiores (Na+, K+, Mg2+, Ca2+, NH4+, Cl-, NO3-, SO4(2-)) e por ICP-MS para quantificação dos elementos traço (Al, Mn, Fe, Pb, Zn, etc.). As espécies químicas que predominaram foram SO4(2-), NO3-, NH4+, Zn, Fe, Al, Ba, Cu, Pb, Mn e Ni em São Paulo, e Na+, K+, Cl-, SO4(2-), Zn e Ni em Cunha. A composição química relacionada com a direção do vento que prevaleceu durante a amostragem, refletiu um transporte de curta escala influenciado pela ocupação do solo e as atividades antrópicas.

The objective of this work was to characterize and compare the chemical composition of the PM10 soluble fraction in relation to meteorological variables such as wind direction and air masses backward trajectories. The PM10 was collected during winter of 1999 in two contrasting sites: the São Paulo city and the State Park of Serra do Mar (Cunha) inside the Atlantic Forest Reserve. The aqueous extracts of PM10 were analyzed by Ion Chromatography for major ions (Na+, K+, Mg2+, Ca2+, NH4+, Cl-, NO3-, SO4(2-)) and by Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) for trace elements (Al, Mn, Fe, Pb, Zn, etc.). In São Paulo, the dominant chemical species were SO4(2-), NO3-, NH4+, Zn, Fe, Al, Ba, Cu, Pb, Mn and Ni while in Cunha, Na+, K+, Cl-, SO4(2-), Zn and Ni were dominant. The chemical composition related to the wind direction during sampling reflected short-range influence due to soil occupation and anthropic activities.

Concentrações anômalas de cromo hexavalente foram detectadas em águas subterrâneas do Aqüífero Adamantina em pelo menos 54 municipalidades localizadas na região noroeste do Estado de São Paulo, sudeste do Brasil, algumas vezes ultrapassando o limite máximo permitido para consumo humano (0,05 mg.L-1). Um estudo foi realizado no município de Urânia, onde as mais elevadas concentrações de cromo da região foram detectadas. A origem da contaminação foi definida como natural, pois foram detectadas concentrações de cromonos arenitos do aqüífero (média 221 ppm) e em piroxênios (6000 ppm), um dos principais minerais pesados encontrados nos sedimentos. Além disso, não foram observadas outras possíveis fontes de contaminação difusas ou pontuais naárea de estudo. Uma estratificação da qualidade da água no aqüífero foi observada e as mais elevadas concentrações de Cr6+ foram detectadas na base do aqüífero (0,12 mg.L-1), onde as águas subterrâneas apresentam valores elevados de potencial redox (Eh = 472,5 mV) e de pH (8,61). A origem do Cr6+ na água deve estar associada com o intemperismo do piroxênio (augita), seguida da oxidação do Cr3+ pelos óxidos de manganês. As maiores concentrações de Cr6+ estão provavelmente ligadas com reações de desorção, devido ao pH anomalamentealcalino da água subterrânea na base do aqüífero.

Anomalous concentrations of hexavalent chromium have been detected in ground-water of the Adamantina Aquifer inat least 54 municipalities located in the northwestern region of the State of São Paulo, southeast Brazil, occasionallyexceeding the permitted limit for human consumption (0.05 mg.L-1). An investigation was conducted in the municipality of Urânia, where the highest concentrations of chromium were detected regionally. It was defined that the originof this contamination is natural, since high concentrations of chromium were detected in aquifer sandstones (averageof 221 ppm) and also in pyroxenes (6000 ppm), one of the main heavy minerals found in the sediments. Besides, noother possible diffuse or point sources of contamination were observed in the study area. Stratification of ground-waterquality was observed and the highest concentrations of Cr6+ were detected at the base of the aquifer (0.12 mg.L-1),where ground-water shows elevated values for redox potential (472.5 mV) and pH (8.61). The origin of Cr6+ in water may be associated with the weathering of pyroxene (augite), followed by the oxidation of Cr3+ by manganese oxides. The highest concentrations of Cr6+ are probably related to desorption reactions, due to the anomalous alkaline pHfound in ground-water at the base of the aquifer.

Estudos sobre a poluição por Hidrocarbonetos Policíclicos Aromáticos (HPAs) são escassos em solos tropicais e no Brasil. Um estudo foi realizado para examinar a composição, as concentrações e fontes de HPAs encontrados em Latossolos vermelho-amarelo (Oxissolos), remanescentes de Mata Atlântica no Estado de São Paulo. As áreas de estudos localizaram-se em um sítio urbano (PEFI) e um natural (CUNHA). A composição granulométrica, pH, teor de matéria orgânica e composição mineralógica foram determinados em amostras de solo superficial. A soma dos HPAs analisados (ΣHPAs) foi 4,5 vezes mais elevada na área urbana do que na área natural. Acenaftileno, acenafteno, fluoreno, fenantreno e fluoranteno foram detectados, em concentrações similares, nos solos das duas áreas. Acenafteno e fluoreno foram os compostos mais abundantes. O pireno foi duas vezes mais abundante no solo da área natural (15 µg.kg-1), e o fluoranteno foi o composto dominante (203 µg.kg-1) na área urbana (6,8 vezes mais elevado que na área natural). Alguns compostos de alto peso molecular, traçadores de emissões veiculares, foram detectados em quantidades significativas no solo da área urbana. O pireno representou 79% da ΣHPAs, enquanto que não foi detectado na área natural. Estes resultados evidenciaram que os solos de floresta em áreas urbanas são caracterizados pela acumulação de HPAs pesados oriundos de emissões industriais e veiculares.

Studies about pollution by Polycyclic Aromatic Hydrocarbons (PAHs) in tropical soils and Brazil are scarce. A study was performed to examine the PAHs composition, concentrations and sources in red-yellow Oxisols of remnant Atlantic Forest of the São Paulo State. Sampling areas were located in an urban site (PEFI) and in a natural one (CUNHA).The granulometric composition, pH, organic matter content and mineralogical composition were determined in samples of superficial soils. The sum of PAHs (ΣHPAs) was 4.5 times higher in the urban area than in the natural one. Acenaphthylene, acenaphthene, fluorene, phenanthrene and fluoranthene have been detected in the soils of both areas and presented similar concentrations. Acenaphthene and fluorene were the most abundant compounds. Pyrene was twice more abundant in the soils of natural area (15 µg.kg-1) than of the urban area and fluoranthene was the dominant compound (203 µg.kg-1) in urban area (6.8 times higher than in the natural area). Some compounds of higher molecular weight, which are tracers of vehicular emissions showed significant concentrations in urban soils. Pyrene represented 79% of ΣPAHs whereas it has not been detected in natural soils. The results showed that forest soils in urban area are characterized by the accumulation of high molecular weight compounds of industrial and vehicular origin.