Distribution of acid-volatile sulfides and simultaneously extracted metals in Guanabara Bay: combination of anthropogenic, sedimentological, and geochemical processes.

Coastal sedimentary systems are affected by continental and marine metal pollutant inputs associated with different hydrodynamic characteristics and geochemical processes. These include the formation of acid-volatile sulfides (AVS) within sediments, which affects metal bioavailability and associated aquatic biota toxicity risks. Physicochemical changes in these environments in the face of extreme natural or man-made environmental influences can dramatically alter metal bioavailability and toxicity through metal binding and immobilization as insoluble sulfides. Surface sediments from Guanabara Bay, river mouths, and two mangrove areas were collected, and AVS and simultaneously extracted metals Cd, Cu, Fe, Mn, Ni, Pb, and Zn and ΣSEM were determined to assess sediment quality. A severe eutrophication history favored AVS concentrations exceeding or close to the sum-SEM concentrations, demonstrating that AVS play an important role in making trace metals unavailable for assimilation by living organisms, mitigating the risks of contamination for the local biota. This eutrophication-driven sulfide accumulation may attenuate the sediment toxicity in sites heavily polluted by metals, while some fewer eutrophic sites became more exposed to metals in excess to AVS.

Assessment of eutrophication from phosphorus remobilization after resuspension of coastal sediments from an urban tropical estuary.

Dredging activities cause sediment resuspension, which can change the bioavailability of nutrients such as phosphorus (P) in aquatic ecosystems due to remobilization. This study evaluated the remobilization of P in the solid and dissolved phase before and after sediment resuspension in the Meriti and Iguaçu River estuaries and the Rio de Janeiro and Niterói harbor in Guanabara Bay (Rio de Janeiro, Brazil). Three water and sediment samples were collected at each point. Dissolved phosphorus (DP), total phosphorus (TP), organic phosphorus (OP), and inorganic phosphorus (IP) were analyzed before and after resuspension. Resuspension directly impacted the fine-grained samples, causing the release of P into the water column after resuspension, increasing eutrophication of the estuary and risk to biota. The phosphorus enrichment index (PEI) was calculated in the four areas, and in all areas, the index was above 1, which means high ecological risk. The area with sandy granulometry and a lower percentage of organic matter showed an increase in the index after resuspension. The resuspension may impact the increase of eutrophication in some areas, due to the remobilization of the sediment and the adsorbed contaminants.

Pyrogenic carbon stocks and its spatial variability in soils from savanna-forest ecotone in amazon.

Forest fragments from Amazon are important long-term carbon (C) reservoirs with an essential role in the global C balance. They are often impacted by understory fires, deforestation, selective logging and livestock. Forest fires convert soil organic matter into pyrogenic carbon (PyC), but little is known about its distribution and accumulation along the soil profile. Thus, the objective of this study is to estimate the refractory carbon stocks derived from PyC accumulated in the soil vertical profile of different seasonal forest fragments in the Amazon. Sixty-nine soil cores (1 m deep) were collected in 12 forest fragments of different sizes considering edge and interior gradients. The mean total organic C (TOC) and PyC contents for the edge and interior gradients were 0.84% and 0.009%, respectively. The PyC/TOC ratio ranged from 0.53% to 1.78%, with an average of 1.32% and increasing in depth, being low when compared with other studies, where the contribution of PyC to TOC ranges from 1 to 9%. PyC stocks on the edge (1.04 ± 0.04 Mg ha-1) differed significantly from the interior (1.46 ± 0.03 Mg ha-1). The analyzed forest fragments presented a weighted PyC stock of 1.37 ± 0.65 Mg ha-1. The vertical distribution of PyC declined in depth with 70% of PyC concentrated in the surface soil layers (0-30 cm). These results indicate that the PyC accumulated in the vertical profile of soils in forest fragments in Amazonia are important, and they need to be considered in Brazilian and global reports on carbon stocks and fluxes.

Tropical forests as drivers of lake carbon burial.

A significant proportion of carbon (C) captured by terrestrial primary production is buried in lacustrine ecosystems, which have been substantially affected by anthropogenic activities globally. However, there is a scarcity of sedimentary organic carbon (OC) accumulation information for lakes surrounded by highly productive rainforests at warm tropical latitudes, or in response to land cover and climate change. Here, we combine new data from intensive campaigns spanning 13 lakes across remote Amazonian regions with a broad literature compilation, to produce the first spatially-weighted global analysis of recent OC burial in lakes (over ~50-100-years) that integrates both biome type and forest cover. We find that humid tropical forest lake sediments are a disproportionately important global OC sink of ~80 Tg C yr-1 with implications for climate change. Further, we demonstrate that temperature and forest conservation are key factors in maintaining massive organic carbon pools in tropical lacustrine sediments.

Using NdSr isotopes in suspended sediments in the Abrolhos coral-reef (SW Atlantic, Brazil) to assess potential contamination from the 2015 Fundão dam collapse.

The Abrolhos bank is home of the richest coral reef system of the Southwestern Atlantic, where endemic coral species are found. It has been reported that Abrolhos' corals are under intense stress due to increasing of Marine Heat Waves during the last decades. Additionally, anthropic interventions along the adjacent coastal regions are a factor of concern since they contribute to the increase in the sediment load and to organic debris input in the reef domain. In November 2015, the collapse of the Fundão mining tailings dam resulted in the release of approximately 50 million m3 of iron oxide and quartz-rich slurry into the Doce River. Aiming at using a fingerprint of the tailings and to assess the presence of traces of the Fundão dam material from this event on the Abrolhos bank, this work presents new 87Sr/86Sr and 143Nd/144Nd isotope ratios of marine suspended sediment samples collected between 2016 and 2020 from a network of sediment traps throughout the reef and complementary suspended material at sea. In parallel, we monitored meteo-oceanographic parameters and modeled surface marine currents as an attempt to identify the sediment transport between the Doce River mouth and Abrolhos bank. The r isotopes were used as provenance proxies based on the fact that minerals and rocks tend to have specific isotopic signatures reflecting their own geological derivation. In this context, the isotopic ratios of various potential regional sources for the sedimentation in Abrolhos bank were evaluated. Our monitoring and isotopic measurements indicate that Doce River signatures are detected at Abrolhos bank, following the seasonal Doce River discharge at sea. Isotopic signature of Doce River at Abrolhos bank was also observed during the austral winter (July-August) when cold fronts migrate at the Brazilian coast with higher frequency and energy.

Ecological risks associated to trace metals of contaminated sediments from a densely urbanized tropical eutrophic estuary.

The sediment contamination by trace metals in coastal aquatic ecosystems is a worldwide environmental problem, since metals can be toxic, persistent, and bioaccumulated. In case of natural events, such as storms, or anthropogenic activities, like dredging, the sediment resuspension to the water column occurs and can solubilize metals, probably increasing their bioavailability and consequently the risk to aquatic life. This study evaluated the bioavailability on reactive trace metals (Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn) in estuarine sediments from Iguaçu and Meriti Rivers, both in the drainage basin of Guanabara Bay (Rio de Janeiro, Brazil). Additionally, a discussion about the anthropogenic interference throughout time of six short sediments cores, calculating three different indexes (contamination factors, CF; potential ecological risk index for a single heavy metal, Eif for short; potential ecological risk, PERI) was performed. It was considered as reactive phase, the metal concentrations obtained using a weak acid extraction (in HCl 1 mol L-1 solution). Zn presented high concentrations after resuspension, being above effect range medium (ERM) (52.81 to 1337.4 mg kg-1). The CF indicated very high contamination degree for Cu (14.62 to 17.96) and Zn (27.80 to 35.85) for both rivers. The Eif for short presented higher risk to Cu and Zn for Iguaçu and Meriti rivers. PERI index classified Meriti River samples as severely contaminated (238.10 to 351.62).

Determination and speciation of cadmium in microcosms with Bunodosoma caissarum and Perna perna using isotopically enriched 116Cd.

The study of the uptake and distribution of elements in marine environments is of great interest for understanding their pathways and accumulation. Here, we investigated in laboratory experiments the accumulation behavior of Cd in the sea anemone Bunodosoma caissarum and the mussel Perna perna. Specimens were incubated with isotopically enriched 116Cd in aquariums. Cd concentrations in the seawater and in the tissues of B. caissarum and P. perna were followed by inductively coupled plasma-mass spectrometry (ICP-MS) by means of isotope dilution analysis. Bioconcentration factors for B. caissarum and P. perna exposed to 0.9µg·L-1 of 116Cd were determined to be 80.5 and 850, respectively. P. perna specimens exposed to 4.5µg·L-1 of 116Cd reached 530. Cytosolic proteins associated with Cd from the tissues were extracted and further analyzed by size-exclusion chromatography coupled to ICP-MS. Cd accumulation could be detected in both organisms ranging from high-molecular to low-molecular species.

Ecological risk evaluation of sediment metals in a tropical Euthrophic Bay, Guanabara Bay, Southeast Atlantic.

Surface sediments were collected from Guanabara Bay, at 14 stations distributed in five sectors, over three sampling campaigns. Analyses of metals, grain size fractions and total organic carbon analyses were performed. The geo-accumulation index and the enrichment factor were estimated to assess contamination status based on background values. Additionally, the sediment quality guidelines were applied to evaluate the adverse biological effects. Results show that there was no seasonal variation in sediment quality based on any methodology, and all methods utilized showed that NW sector and HRJ sector were the worst affected and that the NE sector had the best conditions. The sediments of GB are polluted mainly by Cr, Pb and Zn. According to ΣSEM/AVS, these metals are not available to the biota, although toxicity tests dispute this. Among the various methods employed, those using background values for the area seem to best reflect the local historical contamination.

Mercury distribution, methylation and volatilization in microcosms with and without the sea anemone Bunodosoma caissarum.

Mercury (Hg) has a complex biogeochemical cycle in aquatic environments. Its most toxic form, methylmercury (MeHg), is produced by microorganisms. This study investigated how the sea anemone Bunodosoma caissarum affects Hg distribution, methylation and volatilization in laboratory model systems. (203)Hg was added to microcosms and its distribution in seawater, specimens and air was periodically measured by gamma spectrometry. MeHg was measured by liquid scintillation. After the uptake period, specimens had a bioconcentration factor of 70 and in microcosms with and without B. caissarum, respectively 0.05% and 0.32% of the initial spike was found as MeHg. After depuration, MeHg in specimens ranged from 0.2% to 2.4% of total Hg. Microcosms with B. caissarum had higher Hg volatilization (58%) than controls (17%), possibly due to Hg(2+) reduction mediated by microorganisms associated with its tissues and mucus secretions. Marine organisms and their associated microbiota may play a role in Hg and MeHg cycling.

Mass balance in the monitoring of pollutants in tidal rivers of the Guanabara Bay, Rio de Janeiro, Brazil.

This study addressed the identification and monitoring of pollution sources of terrestrial origin in rivers (domestic sewage and industrial effluents) and critical fluvial segments in highly polluted environments under tidal influence (mixing marine and continental sources) from Guanabara Bay Basin, Rio de Janeiro, Brazil. The mass balance of contaminants was determined in conditions of continuous flow (low tide) during dry season (lower dilution capability). The results allowed the evaluation of the potential of contaminant mass generation by the different river segments and the estimation of their natural and anthropogenic components. The water quality of Iguaçú and Sarapuí Rivers were evaluated for metals and biochemical oxygen demand. The method gave an excellent response, including the possibility of sources identification and contaminated river segments ranking. The approach also offers fast execution and data interpretation, being highly efficient.

Uso dos fenóis da lignina no estudo da matéria orgânica na várzea do Lago Grande Curuái, Pará e no Lago do Caçó, Maranhão, Brasil / Use of lignin phenols in the study of organic matter in the Lago Grande Curuái floodplain, Pará and Lake Caçó, Maranhão, Brazil

ste estudo tem por objetivo caracterizar os sedimentos superficiais, quanto ao seu teor e qualidade dos fenóis da lignina, em dois sistemas lacustres distintos: a Várzea do Lago Grande Curuái (PA) e o Lago do Caçó (MA). A Várzea do Lago Grande Curuái é localizada na margem direita do Rio Amazonas, aproximadamente 850 km da foz e é caracterizada pela presença de lagos de águas brancas e pretas. O Lago do Caçó está localizado no Maranhão, na borda do ecossistema amazônico. Foram realizadas análises da concentração de lignina (λ), carbono orgânico total (COT), nitrogênio e isótopos do carbono (δ13C). Os resultados indicam que os sedimentos superficias de lagos de águas brancas apresentam baixos valores de COT (1,5 a 3,6%), baixa concentração de λ (0,73 a 1,28 mg.100mg CO-1) e alto índice de degradação (0,29 a 2,01). Os sedimentos superficiais de lagos de águas pretas apresentam maiores valores de COT (6,0 a 12,1%) e de λ (1,44 a 1,93 mg.100mg CO-1) em relação aos sedimentos de lagos de águas brancas, porém baixos em comparação com os sedimentos do Lago do Caçó (7,2 ~ 15,3% e 1,83 ~ 4,64 mg .100mg CO-1, respectivamente). Através das análises realizadas foi possível identificar diferentes contribuições de fontes assim como diferentes estados de preservação da matéria orgânica sedimentada nos dois sistemas apresentados.

This study aims to characterize the superficial sediments of lakes in black and white waters of an Amazonian floodplain system in terms of carbon content and quality of lignin phenols. "Várzea do Lago Grande Curuái" floodplain is located on the right bank of the Amazon River about 850 km from the estuary. Superficial sediments samples were compared with superficial samples from Lake Caçó, located in Maranhão, the edge of the Amazon ecosystem. Concentration of lignin (λ), Total Organic Carbon (COT), nitrogen and isotope of carbon (δ13C) were undertaken. The results indicate that, in general, the superficial sediments of lakes of white water have low values of COT (1,5 to 3,6%), low concentrations of λ (0,73 to 1,28 mg.100mg CO-1) and high degradation index (0.29 to 2.01). Superficial sediments of lakes of black water had higher values of COT (6,0 to 12,1%) and λ (1,44 to 1,93 mg.100mg CO-1) than the sediments of lakes of white waters, but lower in comparison with the sediments of Caçó Lake. Through such analysis, it was possible to identify different contributions of organic matter sources and the preservation states to the superficial sediments at both sites.

Origem e dinâmica da deposição dos sedimentos superficiais na Várzea do Lago Grande de Curuai, Pará, Brasil / Source and deposition dynamics of superficial sediments in the "Várzea do Lago Grande de Curuai" floodplain, Pará, Brazil

Este estudo tem por objetivo caracterizar os sedimentos superficiais de um sistema de Várzea do Rio Amazonas, quanto a sua granulometria e ao seu teor orgânico, assim como compreender a origem e a hidrodinâmica destes sedimentos. 51 amostras de sedimento superficial foram coletadas na Várzea do Lago Grande de Curuai, localizada na margem direita do Rio Amazonas à aproximadamente 850km da foz. A granulometria, o teor em carbono orgânico e nitrogênio total, a razão entre o carbono e o nitrogênio (C/N), assim como o isótopo estável do carbono (δ13C) e do nitrogênio (δ15N) foram utilisados para este fim. Este estudo colocou em evidência que os sedimentos da várzea são finos, caracterizados principalmente pela presença de silte (médio à fino), seguido de argila e tem como principal fonte o Rio Amazonas e a Formação Alter do Chão. A presença de areia é pequena e extremamente localizada, próxima as áreas de deságue dos igarapés de terra firme que representam sua maior fonte. O teor de matéria orgânica nestes sedimentos varia entre 1,5 à 37% de carbono. Os resultados do isótopo do carbono (13C) e da razão C/N evidenciam a presença de matéria orgânica composta por diferentes fontes: material orgânico terrígeno, macrofítico, solos, material orgânico transportado pelo rio, e um componente fitoplanctônico.

The main objectives of this study were to characterize superficial sediments of an Amazonian floodplain system, by its size and organic content, and also to understand the local hydrodynamic and sources of these sediments. 51 samples of superficial sediment were collected in the floodplain “Várzea do Lago Grande de Curuai”, located on the right bank of the Amazon River, approximately, 850km from the estuary. The granulometry, the organic carbon and total nitrogen contents, the carbon and nitrogen ratio (C/N), as well as the isotope of carbon (δ13C) and nitrogen (δ15N) were used. This study points out that the sediments of the Curuai floodplain are fine, characterized mainly by the presence of silt (medium to fine), followed by clays. The main sources of these sediments are the Amazon River followed by “Alter do Chão” formation. The presence of sand was extremely located and near the inflow areas of “terra firme” igarapés that are the main source. The organic matter contents ranged between 1.5% and 37% of carbon. On the other hand, the results of 13C and C/N ratio evidence the presence of an organic matter made up of different sources: flooding forest, macrofítes, soil, organic material carried by the River and a phytoplanctonic component.