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Featured researches published by Erika Seidel.


Environmental Pollution | 2018

Unraveling microbial turnover and non-extractable residues of bromoxynil in soil microcosms with 13C-isotope probing

Karolina M. Nowak; Markus Telscher; Erika Seidel; Anja Miltner

Bromoxynil is a widely used nitrile herbicide applied to maize and other cereals in many countries. To date, still little is known about bromoxynil turnover and the structural identity of bromoxynil non-extractable residues (NER) which are reported to occur in high amounts. Therefore, we investigated the microbial turnover of 13C-labeled bromoxynil for 32 days. A focus was laid on the estimation of biogenic NER based on the turnover of 13C into amino acids (AA). At the end, 25% of 13C6-bromoxynil equivalents were mineralized, 2% assigned to extractable residues and 72.5% to NER. Based on 12% in the 13C-total AA and an assumed share of AA of 50% in microbial biomass we arrived at 24% of total 13C-biogenic NER. About 33% of the total 13C-NER could thus be explained by 13C-biogenic NER; 67% was unknown and by definition xenobiotic NER with potential for toxicity. The 13C label from 13C6-bromoxynil was mainly detected in the humic acids (28.5%), but significant amounts were also found in non-humics (17.6%), fulvic acids (13.2%) and humins (12.7%). The 13C-total amino acids hydrolyzed from humic acids, humins and fulvic acids amounted to 5.2%, 6.1% and 1.2% of 13C6-bromoxynil equivalents, respectively, corresponding to total 13C-biogenic NER amounts of 10.4%, 12.2% and 2.4%. The humins contained mostly 13C-biogenic NER, whereas the humic and fulvic acids may be dominated by the xenobiotic NER. Due to the high proportion of unknown 13C-NER and particularly in the humic and fulvic acids, future studies should focus on the detailed characterization of these fractions.


Archive | 2002

Novel thermodynamically stable crystal modification of (2-(2-Chloro-4-mesyl-benzoyl)cyclohexane-1,3-dione)

Axel Eble; Erika Seidel; Britta Olenik; Jordi Benet-Buchholz; Martin-Holger Hinz


Archive | 2003

Crystal modification II of 2-[2-(1-chloro-cyclopropyl)-3-(2-chlorophenyl)-2-hydroxy-propyl]-2,4-dihydro-3H-1,2,4-triazole-3-thione

Erika Seidel; Ronald Vermeer; Karin Hasenack; Britta Olenik


Archive | 2004

Kristallmodifikation II des 2-[2-(Chlor-cyclopropyl)-3-(2-chlorphenyl)-2-hydroxy-propyl]-2,4dihydro-3H-1,2,4-triazol-3-thions

Erika Seidel; Ronald Vermeer; Karin Hasenack; Olenik, Britta, Dipl.-Chem.


Archive | 2003

Crystal form ii of 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-3h-1,2,4-triazole-3-thione

Erika Seidel; Ronald Vermeer; Karin Hasenack; Britta Olenik


Archive | 2003

Kristallmodifikation ii des 2- 2-(1-chlor-cyclopropyl)-3-(2-chlorphenyl)-2-hydroxy-propyl]-2,4-dihydro-3h-1,2,4-triazol-3-thions

Karin Hasenack; Britta Olenik; Erika Seidel; Ronald Vermeer


Archive | 2002

Nouvelle modification crystalline thermodynamiquement stable de (2-(2-Chloro-4-mesyl-benzoyl)cyclohexane-1,3-dione)

Jordi Benet-Buchholz; Axel Eble; Martin-Holger Hinz; Britta Olenik; Erika Seidel


Archive | 2002

Nueva modificacion cristalina termodinamicamente estable de (2-(2-cloro-4-mesil-benzoil)ciclohexano-1,3-diona).

Jordi Benet-Buchholz; Axel Eble; Martin-Holger Hinz; Britta Olenik; Erika Seidel


Archive | 2002

Ny termodynamisk stabil krystalmodifikation af 2-(2-chlor-4-mesylbenzoyl)cyclohexan-1,3-dion

Axel Eble; Erika Seidel; Britta Olenik; Jordi Benet-Buchholz; Martin-Holger Hinz


Archive | 2002

Kristallmodifikation II des 2-[2-(Chlor-cyclopropyl)-3-(2-chlorphenyl)-2-hydroxy-propyl]-2,4dihydro-3H-1,2,4-triazol-3-thions Crystal modification II of 2- [2- (chloro-cyclopropyl) -3- (2-chlorophenyl) -2-hydroxy-propyl] -2,4dihydro-3H-1,2,4-triazole-3-thione

Karin Hasenack; Britta Olenik; Erika Seidel; Ronald Vermeer

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Anja Miltner

Helmholtz Centre for Environmental Research - UFZ

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Karolina M. Nowak

Technical University of Berlin

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