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Investigating levels of organic contaminants in Danube River sediments in Serbia by multi-ratio equilibrium passive sampling

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F19%3A00113354" target="_blank" >RIV/00216224:14310/19:00113354 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://www.sciencedirect.com/science/article/pii/S0048969719338859" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0048969719338859</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.scitotenv.2019.133935" target="_blank" >10.1016/j.scitotenv.2019.133935</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Investigating levels of organic contaminants in Danube River sediments in Serbia by multi-ratio equilibrium passive sampling

  • Popis výsledku v původním jazyce

    The Danube River is a large transboundary river with many tributaries. Pollution from industries, municipal wastewater and navigation is discharged into the river directly or via its tributaries. These discharges can adversely contribute to the water and sediment quality, posing a risk to aquatic life. Contaminants with low water solubility tend to accumulate in suspended solids, which deposit in riverbed sediments. Subsequently, their levels in sediment represent a time integrated sample indicating the pollution in the watercourse. However, total concentrations in sediment do not directly represent the exposure risk to aquatic life as accumulation in sediment heavily depends on its properties, i.e. the amount of organic material and its composition, which is difficult to characterize as any natural material. To provide contaminant concentrations on a defined basis, surface layer riverbed sediment samples collected at eleven locations along the Danube stretch in the territory of Serbia in 2012, were ex-situ (in the laboratory) equilibrated with silicone passive samplers of constant accumulative properties, using the multi-ratio equilibrium passive sampling approach. Contaminant's equilibrium concentrations in passive samplers are mutually comparable in time and space and are better measure for bioavailability than total sediment concentrations. Uptake in the passive sampler converted to equivalent freely dissolved (pore-) water concentrations agreed well with those obtained from surface water passive sampling carried out within the Joint Danube Survey 3 in 2013. Furthermore, equilibrium passive sampler PCB concentrations, converted to lipid-based concentrations, agreed well with concentrations measured in fish sampled in the Danube several years earlier. Out of eleven priority substances, only fluoranthene exceeded the EU EQS in water, while the EQS for biota was exceeded or approached for fluoranthene and benz[a]pyrene, and hexachlorobenzene. (C) 2019 Elsevier B.V. All rights reserved.

  • Název v anglickém jazyce

    Investigating levels of organic contaminants in Danube River sediments in Serbia by multi-ratio equilibrium passive sampling

  • Popis výsledku anglicky

    The Danube River is a large transboundary river with many tributaries. Pollution from industries, municipal wastewater and navigation is discharged into the river directly or via its tributaries. These discharges can adversely contribute to the water and sediment quality, posing a risk to aquatic life. Contaminants with low water solubility tend to accumulate in suspended solids, which deposit in riverbed sediments. Subsequently, their levels in sediment represent a time integrated sample indicating the pollution in the watercourse. However, total concentrations in sediment do not directly represent the exposure risk to aquatic life as accumulation in sediment heavily depends on its properties, i.e. the amount of organic material and its composition, which is difficult to characterize as any natural material. To provide contaminant concentrations on a defined basis, surface layer riverbed sediment samples collected at eleven locations along the Danube stretch in the territory of Serbia in 2012, were ex-situ (in the laboratory) equilibrated with silicone passive samplers of constant accumulative properties, using the multi-ratio equilibrium passive sampling approach. Contaminant's equilibrium concentrations in passive samplers are mutually comparable in time and space and are better measure for bioavailability than total sediment concentrations. Uptake in the passive sampler converted to equivalent freely dissolved (pore-) water concentrations agreed well with those obtained from surface water passive sampling carried out within the Joint Danube Survey 3 in 2013. Furthermore, equilibrium passive sampler PCB concentrations, converted to lipid-based concentrations, agreed well with concentrations measured in fish sampled in the Danube several years earlier. Out of eleven priority substances, only fluoranthene exceeded the EU EQS in water, while the EQS for biota was exceeded or approached for fluoranthene and benz[a]pyrene, and hexachlorobenzene. (C) 2019 Elsevier B.V. All rights reserved.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10511 - Environmental sciences (social aspects to be 5.7)

Návaznosti výsledku

  • Projekt

    Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2019

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Science of the Total Environment

  • ISSN

    0048-9697

  • e-ISSN

  • Svazek periodika

    696

  • Číslo periodika v rámci svazku

    DEC 2019

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    10

  • Strana od-do

    1-10

  • Kód UT WoS článku

    000498798600070

  • EID výsledku v databázi Scopus

    2-s2.0-85070861653