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@PHDTHESIS{Vonberg:484062,
      author       = {Vonberg, David},
      othercontributors = {Rüde, Thomas R. and Vanderborght, Jan},
      title        = {{A}trazine in the environment 20 years after its ban :
                      long-term monitoring of a shallow aquifer (in western
                      {G}ermany) and soil residue analysis},
      volume       = {293},
      school       = {RWTH Aachen},
      type         = {Dissertation},
      address      = {Jülich},
      publisher    = {Forschungszentrum Jülich GmbH, Zentralbibliothek},
      reportid     = {RWTH-2015-04985},
      isbn         = {978-3-95806-099-9},
      series       = {Schriften des Forschungszentrums Jülich. Reihe Energie
                      $\&$ Umwelt = Energy $\&$ environment},
      pages        = {1 Online-Ressource (149 Seiten) : Illustrationen,
                      Diagramme, Karten},
      year         = {2015},
      note         = {Druckausgabe: 2015. - Onlineausgabe: 2015. - Auch
                      veröffentlicht auf dem Publikationsserver der RWTH Aachen
                      University 2016; Dissertation, RWTH Aachen, 2015},
      abstract     = {Atrazine, one of the worldwide most widespread herbicides,
                      was banned in Germany in 1991 and in the European Union in
                      2004, due to findings of atrazine concentrations in ground-
                      and drinking waters exceeding the threshold value of 0.1 µg
                      L-1. Nevertheless atrazine and the metabolite
                      deethylatrazine were still detected in German aquifers more
                      than 10 years after its prohibition, often without any
                      considerable decreasing trend in groundwater concentration.
                      Because atrazine was already found to be persistent in soils
                      for more than two decades after the last application, the
                      hypothesis was raised that a continued release of atrazine
                      residues from the soil into groundwaters might sustain
                      atrazine groundwater concentrations on elevated levels. The
                      overall objective of this study was to investigate the
                      occurrence and concentration trends of atrazine and its main
                      metabolites in the groundwater-soil environment after the
                      prohibition of its use. Accordingly, in this study results
                      of i) 20 years of atrazine groundwater monitoring of a a
                      shallow aquifer in western Germany since its ban and ii)
                      atrazine soil residue analyses in the vadose zone of the
                      same study area 21 years after its ban are presented. The
                      phreatic Zwischenscholle aquifer located in the Lower Rhine
                      Embayment is exposed to intensive agricultural land use and
                      is highly susceptible to contaminants due to a shallow water
                      table. In total 60 observation wells (OWs) have been
                      monitored since 1991, of which 11 are sampled monthly today.
                      Descriptive statistics of monitoring data were derived using
                      the “regression on order statistics” (ROS) data
                      censoring approach, estimating values for nonquantifiable
                      values rather than substitute them by e.g. half of the limit
                      of quantification and taking the risk of biasing statistical
                      parameters. The monitoring data shows that even 20 years
                      after the ban of atrazine, the groundwater concentrations of
                      sampled OWs remain on a level close to the threshold value
                      of 0.1 µg L-1 without any considerable decrease. The
                      spatial distribution of atrazine concentrations is highly
                      heterogeneous with OWs exhibiting permanently concentrations
                      above the regulatory threshold on the one hand and other OWs
                      with concentrations mostly below the limit of quantification
                      (LOQ) on the other hand. Here atrazine concentrations show
                      upward, downward or approximately constant trends. The
                      deethylatrazine-to-atrazine ratio (DAR) was used to
                      distinguish between diffuse – and point-source
                      contaminations. A DAR around unity (slightly smaller for
                      thin vadose zones like for the investigated aquifer)
                      suggests a contamination of an aquifer by diffuse pathways,
                      resulting in significant metabolization of atrazine to
                      deethylatrazine due to a longer contact time to soil
                      microorganisms. Conversely, point-source contaminations
                      where the contaminant enters the aquifer directly by e.g.
                      macropore flow results in negligible deethylation and hence
                      a DAR close to zero. A global mean DAR value of 0.84 for the
                      monitoring data of the Zwischenscholle aquifer indicates
                      mainly diffuse contamination. Also most of the DARs for
                      single observation wells suggest mainly diffuse pollution,
                      except for one OW with a mean DAR of 0.02, clearly
                      indicating point-source contamination. Principle Component
                      Analysis (PCA) of the monitoring dataset demonstrated
                      relationships between the metabolite deisopropylatrazine and
                      its parent compound simazine but not with atrazine, and
                      deethylatrazine, atrazine, nitrate, and the specific
                      electrical conductivity. These parameters indicate diffuse
                      agricultural impacts on groundwater quality. The groundwater
                      monitoring findings point at the difficulty to estimate mean
                      concentrations of contamination for entire aquifers and to
                      evaluate groundwater quality based on average parameters.
                      However, analytical data of monthly sampled single
                      observation wells provide adequate information to
                      characterize local contamination and evolutionary trends of
                      pollutant concentration. For atrazine soil residue analysis
                      three soil cores reaching down to the groundwater table
                      (approximately 3 m below soil surface) were taken in an
                      agricultural field where atrazine was applied prior to its
                      ban. It is uncertain if atrazine was applied in total two or
                      three times with a recommended dose of 0.96 kg ha-1. Eight
                      layers were separated (0-10 cm, 10-30 cm, 30-60 cm, 60-100
                      cm, 100-150 cm, 150-200 cm, 200-250 cm, 250-300 cm) for
                      atrazine residue analysis and soil parameters (grain size
                      distribution, pH, cation exchange capacity (CECeff) and
                      organic carbon content). Soil samples of each layer were
                      extracted using accelerated solvent extraction (ASE) and
                      analyzed by LC-MS/MS analysis. Prior to this analysis, a
                      method validation was conducted to find optimum extraction
                      parameter combinations. For all extractions a methanol/water
                      (4:1, v/v) solvent was used. The highest quantifiable
                      atrazine extraction yield amongst all extraction parameter
                      combinations between 100°C and 135°C and 100 bar, 150 bar
                      and 207 bar was obtained for 100°C and 207 bar. Atrazine
                      yields were generally higher for higher pressures. Possibly
                      the higher pressure facilitates soil matrix penetration by
                      the solvent. Extractions using 135°C and the highest
                      pressure of 207 bar resulted in quantified concentration of
                      atrazine 31 $\%$ lower than those using 100°C. Probably,
                      the higher extraction temperature lead to an increased
                      co-extraction of soil-matrix compounds, which caused a
                      quenching effect and hence less quantifiable atrazine.
                      Extracted atrazine concentrations of the different layers of
                      the soil cores ranged between 0.2 µg kg-1 and 0.01 µg kg-1
                      for topsoil and subsoil, respectively. Averaged residual
                      atrazine accounts for 0.01 $\%$ of the applied mass in the
                      top layer and 0.07 $\%$ in the total soil profile (for in
                      total 3 applications). However, the calculation can only be
                      treated as a conservative estimate, because spatial
                      information of atrazine field applications and the correct
                      number of applications (2 or 3 times) are not available. A
                      complete and instantaneous remobilization of atrazine
                      residues from the unsaturated zone, leaching to and mixing
                      with the entire groundwater body would result in a mean
                      groundwater concentration of 0.002 µg L-1. In contrast,
                      considering local atrazine groundwater contamination below
                      an atrazine residue area by a complete instantaneous
                      remobilization of the latter and vertical mixing with the
                      groundwater body below, atrazine groundwater concentrations
                      would be 0.068 µg L-1. Based on the first scenario, long
                      term leaching of aged atrazine residues from the vadose zone
                      seems to marginally contribute to sustaining average
                      groundwater concentrations of the Zwischenscholle aquifer,
                      which remained constantly close to the threshold limit of
                      0.1 µg L-1 even 20 years after the ban of atrazine. In
                      contrast, the second scenario shows that ongoing local
                      leaching of atrazine from soil residues might result in
                      locally elevated atrazine groundwater concentrations, what
                      might be reflected by the high spatial variability in
                      atrazine groundwater concentrations in the investigated
                      aquifer. A conservative estimate suggests an atrazine
                      half-life value of approximately 2 years for the soil zone,
                      which is significantly higher than the highest atrazine
                      half-life values found in literature (433 days [1.19 years]
                      for top soil). This value only can be taken as rough
                      orientation and most probably underestimates the atrazine
                      half-life time in this soil, because i) non-extractable
                      atrazine could not be included in the calculation and ii)
                      the first two applications were executed before 1991
                      (information of the exact time of application is missing)
                      and iii) for aged atrazine residues and increased resistance
                      to biodegradation, atrazine degradation in soils rather
                      follows multi-rate kinetics than assumed first order
                      kinetics, what could result in an overestimation of decay
                      rates. These findings show that atrazine persistence in the
                      field might be distinctively higher than predicted assuming
                      first-order degradation kinetics and using half-life values
                      obtained from lab experiments which reach a maximum of 433
                      days for topsoils. Generally, literature values for the
                      organic carbon normalized distribution coefficient (KOC) and
                      dissipation half-life value for atrazine show a wide range
                      between 25 and 600 L Kg 1 and a few days up to 433 days.
                      Until now there is a lack of the understanding of how
                      herbicide degradation rates vary according to spatial
                      heterogeneity of soil properties. Furthermore, important
                      determining factors influencing degradation like microbial
                      ecology and its spatial variability have been neglected so
                      far for pesticide fate predictions. Accordingly, the
                      accuracy of model predictions of catchment scale atrazine
                      behavior on the long-term based on first-order-kinetics and
                      standard laboratory-derived sorption parameter values may be
                      not reliable. Thus the risk of long-term adverse
                      environmental effects may be higher than estimated. In
                      consequence, there is a need for more realistic pesticide
                      risk assessments and regulation procedures besides standard
                      models for pesticide fate predictions. Finally, considering
                      the key finding that the persistence of particular
                      pesticides in groundwater may be highly underestimated by
                      pesticide fate predictions based on laboratory short-term
                      studies, contaminant monitoring in the groundwater-soil
                      environment remains of highest importance, to i) detect
                      potential groundwater contaminations, ii) re-consider
                      pesticide fate predictions, iii) limit or ban the use of
                      contaminants frequently exceeding thresholds and iv) treat
                      drinking water adequately.},
      cin          = {532220 / 530000},
      ddc          = {550},
      cid          = {$I:(DE-82)532220_20140620$ / $I:(DE-82)530000_20140620$},
      typ          = {PUB:(DE-HGF)11 / PUB:(DE-HGF)3},
      urn          = {urn:nbn:de:hbz:82-rwth-2015-049853},
      url          = {https://publications.rwth-aachen.de/record/484062},
}