Photolytic transformation products and biological stability of the hydrological tracer Uranine

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Photolytic transformation products and biological stability of the hydrological tracer Uranine. / Gutowski, Lukasz; Olsson, Oliver; Lange, Jens et al.
In: The Science of The Total Environment, Vol. 533, 15.11.2015, p. 446-453.

Research output: Journal contributionsJournal articlesResearchpeer-review

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@article{89a8e05ca835466ebe4e89cb854849dc,
title = "Photolytic transformation products and biological stability of the hydrological tracer Uranine",
abstract = "Among many fluorescence tracers, Uranine (sodium fluorescein, UR) has most widely been used in hydrological research. Extensive use of UR for tracing experiments or commercial use might cause a potential risk of long-term environmental contamination. As any organic substance released to the environment, also UR is subjected to chemical and physical reactions that can be chemical, biological and photolysis processes. These processes transform the parent compound (PC) and have not been extensively investigated for UR. This study applies two OECDs (301 D and 301 F) tests and a screening water sediment test (WST) to investigate the biodegradability of the PC. Photolysis in water was explored by Xe lamp irradiation. Subsequently, the biodegradability of the photolysis mixtures was examined. The primary elimination of UR was monitored and structures of its transformation products (TPs) were elucidated by HPLC-FLD-MS/MS. UR was found not readily biodegradable, although small degradation rates could be observed in the OECD 301 D and WST. HPLC-FLD analysis showed high primary elimination of the tracer during photolysis. However, the low degree of mineralization found indicates that the UR was not fully degraded, instead transformed to TPs. A total of 5 photo-TPs were identified. According to MS/MS data, chemical structures could be proposed for all identified photo-TPs. Likewise the parent compound it was demonstrated that photo-TPs were largely recalcitrant to microbial degradation. Although we did not find indications for toxicity, target-oriented studies on the environmental impact of these photo-TPs are warranted. Results obtained in this study show that deeper investigations are necessary to fully understand fate and risk connected to the use of UR.",
keywords = "Chemistry, Uranine, Biodegradation, Photodegradation, Closed Bottle Test, Water Sediment Test, Transformation product, Oxitop",
author = "Lukasz Gutowski and Oliver Olsson and Jens Lange and Klaus K{\"u}mmerer",
note = "Copyright {\textcopyright} 2015 Elsevier B.V. All rights reserved.",
year = "2015",
month = nov,
day = "15",
doi = "10.1016/j.scitotenv.2015.07.002",
language = "English",
volume = "533",
pages = "446--453",
journal = "The Science of The Total Environment",
issn = "0048-9697",
publisher = "Elsevier B.V.",

}

RIS

TY - JOUR

T1 - Photolytic transformation products and biological stability of the hydrological tracer Uranine

AU - Gutowski, Lukasz

AU - Olsson, Oliver

AU - Lange, Jens

AU - Kümmerer, Klaus

N1 - Copyright © 2015 Elsevier B.V. All rights reserved.

PY - 2015/11/15

Y1 - 2015/11/15

N2 - Among many fluorescence tracers, Uranine (sodium fluorescein, UR) has most widely been used in hydrological research. Extensive use of UR for tracing experiments or commercial use might cause a potential risk of long-term environmental contamination. As any organic substance released to the environment, also UR is subjected to chemical and physical reactions that can be chemical, biological and photolysis processes. These processes transform the parent compound (PC) and have not been extensively investigated for UR. This study applies two OECDs (301 D and 301 F) tests and a screening water sediment test (WST) to investigate the biodegradability of the PC. Photolysis in water was explored by Xe lamp irradiation. Subsequently, the biodegradability of the photolysis mixtures was examined. The primary elimination of UR was monitored and structures of its transformation products (TPs) were elucidated by HPLC-FLD-MS/MS. UR was found not readily biodegradable, although small degradation rates could be observed in the OECD 301 D and WST. HPLC-FLD analysis showed high primary elimination of the tracer during photolysis. However, the low degree of mineralization found indicates that the UR was not fully degraded, instead transformed to TPs. A total of 5 photo-TPs were identified. According to MS/MS data, chemical structures could be proposed for all identified photo-TPs. Likewise the parent compound it was demonstrated that photo-TPs were largely recalcitrant to microbial degradation. Although we did not find indications for toxicity, target-oriented studies on the environmental impact of these photo-TPs are warranted. Results obtained in this study show that deeper investigations are necessary to fully understand fate and risk connected to the use of UR.

AB - Among many fluorescence tracers, Uranine (sodium fluorescein, UR) has most widely been used in hydrological research. Extensive use of UR for tracing experiments or commercial use might cause a potential risk of long-term environmental contamination. As any organic substance released to the environment, also UR is subjected to chemical and physical reactions that can be chemical, biological and photolysis processes. These processes transform the parent compound (PC) and have not been extensively investigated for UR. This study applies two OECDs (301 D and 301 F) tests and a screening water sediment test (WST) to investigate the biodegradability of the PC. Photolysis in water was explored by Xe lamp irradiation. Subsequently, the biodegradability of the photolysis mixtures was examined. The primary elimination of UR was monitored and structures of its transformation products (TPs) were elucidated by HPLC-FLD-MS/MS. UR was found not readily biodegradable, although small degradation rates could be observed in the OECD 301 D and WST. HPLC-FLD analysis showed high primary elimination of the tracer during photolysis. However, the low degree of mineralization found indicates that the UR was not fully degraded, instead transformed to TPs. A total of 5 photo-TPs were identified. According to MS/MS data, chemical structures could be proposed for all identified photo-TPs. Likewise the parent compound it was demonstrated that photo-TPs were largely recalcitrant to microbial degradation. Although we did not find indications for toxicity, target-oriented studies on the environmental impact of these photo-TPs are warranted. Results obtained in this study show that deeper investigations are necessary to fully understand fate and risk connected to the use of UR.

KW - Chemistry

KW - Uranine

KW - Biodegradation

KW - Photodegradation

KW - Closed Bottle Test

KW - Water Sediment Test

KW - Transformation product

KW - Oxitop

UR - http://www.scopus.com/inward/record.url?scp=84938504462&partnerID=8YFLogxK

U2 - 10.1016/j.scitotenv.2015.07.002

DO - 10.1016/j.scitotenv.2015.07.002

M3 - Journal articles

C2 - 26179782

VL - 533

SP - 446

EP - 453

JO - The Science of The Total Environment

JF - The Science of The Total Environment

SN - 0048-9697

ER -

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