Nathan Barros
Universidade Federal de Juiz de Fora
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Applied and Environmental Microbiology | 2010
Nathan Barros; Vinicius F. Farjalla; Maria Carolina S. Soares; Rossana C. N. Melo; Fábio Roland
ABSTRACT The importance of viruses in aquatic ecosystem functioning has been widely described. However, few studies have examined tropical aquatic ecosystems. Here, we evaluated for the first time viruses and their relationship with other planktonic communities in an Amazonian freshwater ecosystem. Coupling between viruses and bacteria was studied, focusing both on hydrologic dynamics and anthropogenic forced turbidity in the system (Lake Batata). Samples were taken during four hydrologic seasons at both natural and impacted sites to count virus-like particles (VLP) and bacteria. In parallel, virus-infected bacteria were identified and quantified by transmission electron microscopy (TEM). Viral abundance ranged from 0.5 × 107 ± 0.2 × 107 VLP ml−1 (high-water season, impacted site) to 1.7 × 107 ± 0.4 × 107 VLP ml−1 (low-water season, natural site). These data were strongly correlated with the bacterial abundance (r2 = 0.84; P < 0.05), which ranged from 1.0 × 106 ± 0.5 × 106 cells ml−1 (high water, impacted site) to 3.4 × 106 ± 0.7 × 106 cells ml−1 (low water, natural site). Moreover, the viral abundance was weakly correlated with chlorophyll a, suggesting that most viruses were bacteriophages. TEM quantitative analyses revealed that the frequency of visibly infected cells was 20%, with 10 ± 3 phages per cell section. In general, we found a low virus-bacterium ratio (<7). Both the close coupling between the viral and bacterial abundances and the low virus-bacterium ratio suggest that viral abundance tends to be driven by the reduction of hosts for viral infection. Our results demonstrate that viruses are controlled by biological substrates, whereas in addition to grazing, bacteria are regulated by physical processes caused by turbidity, which affect underwater light distribution and dissolved organic carbon availability.
Frontiers in Microbiology | 2016
Rafael M. Almeida; Gabriel N. Nóbrega; Pedro C. Junger; Aline V. Figueiredo; Anízio S. Andrade; Caroline G. B. de Moura; Denise Tonetta; Ernandes S. Oliveira; Fabiana Araújo; Felipe Rust; Juan M. Piñeiro-Guerra; Jurandir Rodrigues de Mendonça; Leonardo R. Medeiros; Lorena Pinheiro; Marcela Miranda; Mariana R. A. Costa; Michaela L. Melo; Regina L. G. Nobre; Thiago Benevides; Fábio Roland; Jeroen J. M. de Klein; Nathan Barros; Raquel Mendonça; Vanessa Becker; Vera L. M. Huszar; Sarian Kosten
Recent studies from temperate lakes indicate that eutrophic systems tend to emit less carbon dioxide (CO2) and bury more organic carbon (OC) than oligotrophic ones, rendering them CO2 sinks in some cases. However, the scarcity of data from tropical systems is critical for a complete understanding of the interplay between eutrophication and aquatic carbon (C) fluxes in warm waters. We test the hypothesis that a warm eutrophic system is a source of both CO2 and CH4 to the atmosphere, and that atmospheric emissions are larger than the burial of OC in sediments. This hypothesis was based on the following assumptions: (i) OC mineralization rates are high in warm water systems, so that water column CO2 production overrides the high C uptake by primary producers, and (ii) increasing trophic status creates favorable conditions for CH4 production. We measured water-air and sediment-water CO2 fluxes, CH4 diffusion, ebullition and oxidation, net ecosystem production (NEP) and sediment OC burial during the dry season in a eutrophic reservoir in the semiarid northeastern Brazil. The reservoir was stratified during daytime and mixed during nighttime. In spite of the high rates of primary production (4858 ± 934 mg C m-2 d-1), net heterotrophy was prevalent due to high ecosystem respiration (5209 ± 992 mg C m-2 d-1). Consequently, the reservoir was a source of atmospheric CO2 (518 ± 182 mg C m-2 d-1). In addition, the reservoir was a source of ebullitive (17 ± 10 mg C m-2 d-1) and diffusive CH4 (11 ± 6 mg C m-2 d-1). OC sedimentation was high (1162 mg C m-2 d-1), but our results suggest that the majority of it is mineralized to CO2 (722 ± 182 mg C m-2 d-1) rather than buried as OC (440 mg C m-2 d-1). Although temporally resolved data would render our findings more conclusive, our results suggest that despite being a primary production and OC burial hotspot, the tropical eutrophic system studied here was a stronger CO2 and CH4 source than a C sink, mainly because of high rates of OC mineralization in the water column and sediments.
Archive | 2012
Raquel Mendonça; Nathan Barros; Luciana O. Vidal; Felipe S. Pacheco; Sarian Kosten; Fábio Roland
Greenhouse Gas Emissions from Hydroelectric Reservoirs: What Knowledge Do We Have and What is Lacking?
Frontiers in Microbiology | 2015
Rafael de Almeida; Fábio Roland; Simone J. Cardoso; Vinicius F. Farjalla; Reinaldo Luiz Bozelli; Nathan Barros
In response to the massive volume of water along the Amazon River, the Amazon tributaries have their water backed up by 100s of kilometers upstream their mouth. This backwater effect is part of the complex hydrodynamics of Amazonian surface waters, which in turn drives the variation in concentrations of organic matter and nutrients, and also regulates planktonic communities such as viruses and bacteria. Viruses and bacteria are commonly tightly coupled to each other, and their ecological role in aquatic food webs has been increasingly recognized. Here, we surveyed viral and bacterial abundances (BAs) in 26 floodplain lakes along the Trombetas River, the largest clear-water tributary of the Amazon River’s north margin. We correlated viral and BAs with temperature, pH, dissolved inorganic carbon, dissolved organic carbon (DOC), phosphorus, nitrogen, turbidity, water transparency, partial pressure of carbon dioxide (pCO2), phytoplankton abundance, and distance from the lake mouth until the confluence of the Trombetas with the Amazon River. We hypothesized that both bacterial and viral abundances (VAs) would change along a latitudinal gradient, as the backwater effect becomes more intense with increased proximity to the Amazon River; different flood duration and intensity among lakes and waters with contrasting sources would cause spatial variation. Our measurements were performed during the low water period, when floodplain lakes are in their most lake-like conditions. Viral and BAs, DOC, pCO2, and water transparency increased as distance to the Amazon River increased. Most viruses were bacteriophages, as viruses were strongly linked to bacteria, but not to phytoplankton. We suggest that BAs increase in response to DOC quantity and possibly quality, consequently leading to increased VAs. Our results highlight that hydrodynamics plays a key role in the regulation of planktonic viral and bacterial communities in Amazonian floodplain lakes.
Nature Communications | 2017
Ralf Aben; Nathan Barros; Ellen Van Donk; Thijs Frenken; Sabine Hilt; Garabet Kazanjian; Leon P. M. Lamers; E.T.H.M. Peeters; J.G.M. Roelofs; Lisette N. de Senerpont Domis; Susanne Stephan; Mandy Velthuis; Dedmer B. Van de Waal; Martin Wik; Brett F. Thornton; Jeremy Wilkinson; Tonya DelSontro; Sarian Kosten
Methane (CH4) strongly contributes to observed global warming. As natural CH4 emissions mainly originate from wet ecosystems, it is important to unravel how climate change may affect these emissions. This is especially true for ebullition (bubble flux from sediments), a pathway that has long been underestimated but generally dominates emissions. Here we show a remarkably strong relationship between CH4 ebullition and temperature across a wide range of freshwater ecosystems on different continents using multi-seasonal CH4 ebullition data from the literature. As these temperature–ebullition relationships may have been affected by seasonal variation in organic matter availability, we also conducted a controlled year-round mesocosm experiment. Here 4 °C warming led to 51% higher total annual CH4 ebullition, while diffusion was not affected. Our combined findings suggest that global warming will strongly enhance freshwater CH4 emissions through a disproportional increase in ebullition (6–20% per 1 °C increase), contributing to global warming.The impacts of climate change on natural methane (CH4) emissions via ebullition are unclear. Here, using published and experimental multi-seasonal CH4 ebullition data, the authors find a strong relationship between CH4 ebullition and temperature across a wide range of freshwater ecosystems globally.
Ecosystems | 2018
Yves T. Prairie; Jukka Alm; Jake J. Beaulieu; Nathan Barros; Tom J. Battin; Jonathan J. Cole; Paul A. del Giorgio; Tonya DelSontro; Frédéric Guérin; Atle Harby; John A. Harrison; Sara Mercier-Blais; Dominique Serça; Sebastian Sobek; Dominic Vachon
Freshwater reservoirs are a known source of greenhouse gas (GHG) to the atmosphere, but their quantitative significance is still only loosely constrained. Although part of this uncertainty can be attributed to the difficulties in measuring highly variable fluxes, it is also the result of a lack of a clear accounting methodology, particularly about what constitutes new emissions and potential new sinks. In this paper, we review the main processes involved in the generation of GHG in reservoir systems and propose a simple approach to quantify the reservoir GHG footprint in terms of the net changes in GHG fluxes to the atmosphere induced by damming, that is, ‘what the atmosphere sees.’ The approach takes into account the pre-impoundment GHG balance of the landscape, the temporal evolution of reservoir GHG emission profile as well as the natural emissions that are displaced to or away from the reservoir site resulting from hydrological and other changes. It also clarifies the portion of the reservoir carbon burial that can potentially be considered an offset to GHG emissions.
Inland Waters | 2015
Rafael M. Almeida; Lars J. Tranvik; Vera L. M. Huszar; Sebastian Sobek; Raquel Mendonça; Nathan Barros; Gina Boemer; João Durval Arantes; Fábio Roland
Abstract Originating in the Bolivian and Peruvian Andes, the Madeira River is the largest tributary of the Amazon River in terms of discharge. Andean rivers transport large quantities of nutrient-rich suspended sediments and are the main source of phosphorus (P) to the Amazon basin. Here, we show the seasonal variability in concentrations and loads of different P forms (total, particulate, dissolved, and soluble reactive P) in the Madeira River through 8 field campaigns between 2009 and 2011. At our sampling reach in Porto Velho, Brazil, the Madeira River transports ~177–247 Gg yr−1 of P, mostly linked to particles (~85%). Concentrations and loads of all P forms have a maximum at rising waters and a minimum at low waters. Total P concentrations were substantially higher at a given discharge at rising water than at a similar discharge at falling water. The peak of P concentrations matched the peak of rainfall in the upper basin, suggesting an influence of precipitation-driven erosion. Projected precipitation increase in the eastern slopes of the Andes could enhance sediment yield and hence the P transport in the Madeira River. Because most of the P is particulate, however, we hypothesize that the planned proliferation of hydropower dams in the Madeira basin has the potential to reduce P loads substantially, possibly counteracting any precipitation-related increases. In the long term, this could be detrimental to highly productive downstream floodplain forests that are seasonally fertilized with P-rich deposits.
Environmental Science & Technology | 2018
José R. Paranaíba; Nathan Barros; Raquel Mendonça; Annika Linkhorst; Anastasija Isidorova; Fábio Roland; Rafael M. Almeida; Sebastian Sobek
The magnitude of diffusive carbon dioxide (CO2) and methane (CH4) emission from man-made reservoirs is uncertain because the spatial variability generally is not well-represented. Here, we examine the spatial variability and its drivers for partial pressure, gas-exchange velocity (k), and diffusive flux of CO2 and CH4 in three tropical reservoirs using spatially resolved measurements of both gas concentrations and k. We observed high spatial variability in CO2 and CH4 concentrations and flux within all three reservoirs, with river inflow areas generally displaying elevated CH4 concentrations. Conversely, areas close to the dam are generally characterized by low concentrations and are therefore not likely to be representative for the whole system. A large share (44–83%) of the within-reservoir variability of gas concentration was explained by dissolved oxygen, pH, chlorophyll, water depth, and within-reservoir location. High spatial variability in k was observed, and kCH4 was persistently higher (on average, 2.5 times more) than kCO2. Not accounting for the within-reservoir variability in concentrations and k may lead to up to 80% underestimation of whole-system diffusive emission of CO2 and CH4. Our findings provide valuable information on how to develop field-sampling strategies to reliably capture the spatial heterogeneity of diffusive carbon fluxes from reservoirs.
Chemosphere | 2019
Gabrielle R. Quadra; Fábio Roland; Nathan Barros; Olaf Malm; A. S. Lino; Guilherme M. Azevedo; José Ricardo Thomaz; Larissa Fonseca Andrade-Vieira; Milene Miranda Praça-Fontes; Rafael M. Almeida; Raquel Mendonça; Simone J. Cardoso; Yago S. Guida; José Marcello Salabert de Campos
On November 2015, one of Brazils most important watersheds was impacted by the mine waste from Fundão dam collapse in Mariana. The mine waste traveled over 600 km along the Doce River before reaching the sea, causing severe devastation along its way. Here we assessed trace element concentrations and cytogenotoxic effects of the released mine waste. Water samples were collected along the Doce River ten days after the disaster in two impacted sites and one non-impacted site. Sampling points were located hundreds of kilometers downstream of the collapsed dam. Water samples were used for trace element quantification and to run an experiment using Allium cepa to test cytogenotoxicity. We found extremely high concentrations of particulate Fe, Al, and Mn in the impacted sites. We observed cytogenotoxic effects such as alterations in mitotic and phase indexes, and enhanced frequency of chromosomal aberrations. Our results indicate interferences in the cell cycle in impacted sites located hundreds of kilometers downstream of the disaster. The environmental impacts of the dam collapse may not only be far-reaching but also very likely long-lasting, because the mine waste may persist in the Doce River sediment for decades.
Inland Waters | 2018
Sarian Kosten; Sanne W. van den Berg; Raquel Mendonça; José R. Paranaíba; Fábio Roland; Sebastian Sobek; Jamon Van Den Hoek; Nathan Barros
ABSTRACT Although previous studies suggest that greenhouse gas (GHG) emissions from reservoir sediment exposed to the atmosphere during drought may be substantial, this process has not been rigorously quantified. Here we determined carbon dioxide (CO2) and methane (CH4) emissions from sediment cores exposed to a drying and rewetting cycle. We found a strong temporal variation in GHG emissions with peaks when the sediment was drained (C emissions from permanently wet sediment and drained sediments were, respectively, 251 and 1646 mg m−2 d−1 for CO2 and 0.8 and 547.4 mg m−2 d−1 for CH4) and then again during rewetting (C emissions from permanently wet sediment and rewetted sediments were, respectively, 456 and 1725mg m−2 d−1 for CO2 and 1.3 and 3.1 mg m−2 d−1 for CH4). To gain insight into the importance of these emissions at a regional scale, we used Landsat satellite imagery to upscale our results to all Brazilian reservoirs. We found that during the extreme drought of 2014–2015, an additional 1299 km2 of sediment was exposed, resulting in an estimated emission of 8.5 × 1011 g of CO2-eq during the first 15 d after the overlying water disappeared and in the first 33 d after rewetting, the same order of magnitude as the year-round GHG emissions of large (∼mean surface water area 454 km2) Brazilian reservoirs, excluding the emissions from the draw-down zone. Our estimate, however, has high uncertainty, with actual emissions likely higher. We therefore argue that the effects of drought on reservoir GHG emissions merits further study, especially because climate models indicate an increase in the frequency of severe droughts in the future. We recommend incorporation of emissions during drying and rewetting into GHG budgets of reservoirs to improve regional GHG emission estimates and to enable comparison between GHG emissions from hydroelectric and other electricity sources. We also emphasize that peak emissions at the onset of drought and the later rewetting should be quantified to obtain reliable emission estimates.