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  • 1
    In: Hydrogeology Journal, Springer Science and Business Media LLC, Vol. 29, No. 3 ( 2021-05), p. 1153-1171
    Abstract: Nas últimas décadas, os sistemas fraturados e cársticos de águas subterrâneas têm sido intensamente estudados devido à sua alta vulnerabilidade à contaminação por nitrato (NO 3 − ), mas os processos de transformação do nitrogênio (N) dentro da área de recarga ainda são mal compreendidos. Este estudo investigou o papel da área de recarga carstificada na transferência e transformação do NO 3− combinando análises isotópicas do NO 3 − e nitrito (NO 2 − ) com dados de séries temporais de cargas hidráulicas e condutividade elétrica específica de poços de monitoramento de águas subterrâneas e nascente cárstica na Alemanha. Observou-se grande variabilidade espacial das águas subterrâneas nas concentrações de NO 3 − (0.1 a 0.8 mM), o que não pode ser explicado apenas pelo uso agrícola. As medidas de isótopos de abundância natural N e O de N 3 − (δ 15 Ne δ 18 O) confirmam que o NO 3 − deriva principalmente de aplicações de estrume ou fertilizante. A eliminação fracionária de N por denitrificação é indicada por altos valores de δ 15 N e δ 18 O-NO 3 − , elevadas concentrações de NO 2 − (0.05–0.14 mM), e δ 15 N-NO 2 − , valores que foram sistematicamente inferiores aos valores correspondentes de δ 15 N-NO 3 − . Padrões hidráulicos e químicos de resposta de poços de água subterrânea sugerem que eventos de chuva resultam no deslocamento de água de compartimentos de armazenamento transientes, como o epicarste ou a rede de fraturas da zona freática. Embora os níveis de O 2 das águas subterrâneas investigadas estivessem próximos à saturação, a denitrificação local poderia ser promovida em nichos microóxicos ou anoxicos formados no ferro em formações rochosas de carbonatos ferrosos. Os resultados revelaram que (temporariamente) redes de fraturas saturadas na zona freática e o epicarste podem desempenhar um papel importante na transformação durante a recarga de aquíferos fraturados.
    Type of Medium: Online Resource
    ISSN: 1431-2174 , 1435-0157
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2021
    detail.hit.zdb_id: 1481470-5
    SSG: 13
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  • 2
    In: Hydrogeology Journal, Springer Science and Business Media LLC, Vol. 30, No. 1 ( 2022-02), p. 163-180
    Abstract: A redução de nitrato constitui um importante mecanismo natural para mitigar a contaminação generalizada e persistente de nitrato dos recursos hídricos subterrâneos. Em aquíferos fraturados, no entanto, a abundância e acessibilidade de doadores de elétrons e sua correlação espacial com os caminhos do fluxo de água subterrânea são frequentemente mal compreendidos. Neste estudo, o potencial de redução de nitrato de um aquífero carbonato fraturado no Muschelkalk Superior do SO da Alemanha foi investigado, onde a desnitrificação é devido à oxidação do ferro ferroso e enxofre reduzido. As análises petrográficas de amostras de rocha revelaram concentrações de pirita sin-sedimentar e diageneticamente formada variando de 1 a 4% em peso, com apenas pequenas diferenças entre os diferentes tipos de fácies. Ferro ferroso adicional está disponível em dolomitas de sela (até 2.6% em peso), que provavelmente foram formadas por percolação tectonicamente induzida de fluidos hidrotérmicos de baixa temperatura. O registro de furos em poços de água subterrânea (medidor de vazão, vídeo, gama) indica que a maior parte do fluxo de água subterrânea ocorre ao longo de planos de estratificação carstificados parcialmente localizados dentro de dolomitos do cardume e fácies de fundo de poço. A alta porosidade (15–30%) dessas fácies facilita a troca molecular difusiva de solutos entre os caminhos de fluxo nas fraturas e os minerais reativos na matriz de poros. Fácies de alta porosidade, juntamente com as fraturas hidraulicamente ativas com precipitados de pirita ou dolomita em sela, constituem as zonas de maior potencial de redução de nitrato dentro do aquífero. Estimativas baseadas em modelo de balanços aceitador/doador de elétrons indicam que o potencial de redução de nitrato que protege os poços de abastecimento de água aumenta com o aumento da porosidade da matriz de rocha e diminui com o aumento da condutividade hidráulica (ou abertura de fratura efetiva) e espaçamento da rede de fratura.
    Type of Medium: Online Resource
    ISSN: 1431-2174 , 1435-0157
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2022
    detail.hit.zdb_id: 1481470-5
    SSG: 13
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  • 3
    In: Hydrological Processes, Wiley, Vol. 36, No. 2 ( 2022-02)
    Abstract: Lower‐order streams (first‐ and second‐order) define the initial, landscape‐related, chemical signature of stream water in catchments. To date, first‐order streams have been perceived as predominantly draining systems, which collect water and solutes from the surrounding groundwater and surface runoff and simply mirror the chemical composition of the inputs. In this study, the impact of stream‐groundwater exchange fluxes on water chemistry of a first order agricultural stream (Schönbrunnen) and its connected groundwater in south‐western Germany was assessed combining 222 Rn, dissolved ions (chloride, sulphate, nitrate), and salt tracer tests with investigations of stream discharge and groundwater hydraulic gradients. The findings suggest that stream‐water chemistry in lower‐order streams is governed by an intricate interplay between dynamic, bidirectional water and solute exchange between groundwater and the stream leading to a pronounced hydrologic turnover along the studied reaches. High nitrate concentrations (up to 79 mg/L as NO 3 − ) in stream water were attenuated in downstream direction (a mean value of 39 mg/L) without an increase in discharge, suggesting that redox processes occurring during sediment passage in sequential infiltration and exfiltration zones affect stream water chemistry. Nitrate in stream water infiltrating into the aquifer at distinct losing spots was subject to denitrification within the first few decimetres of the streambed, while concurrent exfiltration of low‐nitrate groundwater into the stream at gaining spots compensated for flow losses and in turn diluted instream nitrate concentrations. In summary the findings imply that (1) instream mixing resulting from the bidirectional exchange of water between groundwater and the stream (hydrologic turnover) affects instream nitrate concentrations, (2) denitrification in the streambed of losing reaches and the near‐stream aquifer significantly contributes to reactive nitrate turnover and elimination, and (3) oxidation of ammonium could be a secondary source of nitrate inputs into the stream.
    Type of Medium: Online Resource
    ISSN: 0885-6087 , 1099-1085
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 1479953-4
    SSG: 14
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  • 4
    In: Water Research, Elsevier BV, Vol. 217 ( 2022-06), p. 118334-
    Type of Medium: Online Resource
    ISSN: 0043-1354
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2022
    detail.hit.zdb_id: 202613-2
    detail.hit.zdb_id: 1501098-3
    SSG: 14
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  • 5
    In: Science of The Total Environment, Elsevier BV, Vol. 926 ( 2024-05), p. 172062-
    Type of Medium: Online Resource
    ISSN: 0048-9697
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2024
    detail.hit.zdb_id: 1498726-0
    detail.hit.zdb_id: 121506-1
    SSG: 12
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  • 6
    In: Applied and Environmental Microbiology, American Society for Microbiology, Vol. 87, No. 16 ( 2021-07-27)
    Abstract: Nitrate removal in oligotrophic environments is often limited by the availability of suitable organic electron donors. Chemolithoautotrophic bacteria may play a key role in denitrification in aquifers depleted in organic carbon. Under anoxic and circumneutral pH conditions, iron(II) was hypothesized to serve as an electron donor for microbially mediated nitrate reduction by Fe(II)-oxidizing (NRFeOx) microorganisms. However, lithoautotrophic NRFeOx cultures have never been enriched from any aquifer, and as such, there are no model cultures available to study the physiology and geochemistry of this potentially environmentally relevant process. Using iron(II) as an electron donor, we enriched a lithoautotrophic NRFeOx culture from nitrate-containing groundwater of a pyrite-rich limestone aquifer. In the enriched NRFeOx culture that does not require additional organic cosubstrates for growth, within 7 to 11 days, 0.3 to 0.5 mM nitrate was reduced and 1.3 to 2 mM iron(II) was oxidized, leading to a stoichiometric NO 3 − /Fe(II) ratio of 0.2, with N 2 and N 2 O identified as the main nitrate reduction products. Short-range ordered Fe(III) (oxyhydr)oxides were the product of iron(II) oxidation. Microorganisms were observed to be closely associated with formed minerals, but only few cells were encrusted, suggesting that most of the bacteria were able to avoid mineral precipitation at their surface. Analysis of the microbial community by long-read 16S rRNA gene sequencing revealed that the culture is dominated by members of the Gallionellaceae family that are known as autotrophic, neutrophilic, and microaerophilic iron(II) oxidizers. In summary, our study suggests that NRFeOx mediated by lithoautotrophic bacteria can lead to nitrate removal in anthropogenically affected aquifers. IMPORTANCE Removal of nitrate by microbial denitrification in groundwater is often limited by low concentrations of organic carbon. In these carbon-poor ecosystems, nitrate-reducing bacteria that can use inorganic compounds such as Fe(II) (NRFeOx) as electron donors could play a major role in nitrate removal. However, no lithoautotrophic NRFeOx culture has been successfully isolated or enriched from this type of environment, and as such, there are no model cultures available to study the rate-limiting factors of this potentially important process. Here, we present the physiology and microbial community composition of a novel lithoautotrophic NRFeOx culture enriched from a fractured aquifer in southern Germany. The culture is dominated by a putative Fe(II) oxidizer affiliated with the Gallionellaceae family and performs nitrate reduction coupled to Fe(II) oxidation leading to N 2 O and N 2 formation without the addition of organic substrates. Our analyses demonstrate that lithoautotrophic NRFeOx can potentially lead to nitrate removal in nitrate-contaminated aquifers.
    Type of Medium: Online Resource
    ISSN: 0099-2240 , 1098-5336
    RVK:
    Language: English
    Publisher: American Society for Microbiology
    Publication Date: 2021
    detail.hit.zdb_id: 223011-2
    detail.hit.zdb_id: 1478346-0
    SSG: 12
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