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Volltext : R&D-Project - Identification of organic compounds in the North and Baltic Seas

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Figure  22:  Principal  component  plots  of  the  factor  analysis  of  the  congener  group  composition  of  sPCA
(A)  and  mPCA  (B)  in  technical  mixtures  from  European  producers  and  sediments  from  the
North  and  Baltic  Sea  (  years  2001-2002).  Results  were  obtained  by  CH4/CH2CI2-NICI-MS.  Two
groups  with  related  patterns  are  marked  for  sPCAs  120
Figure  23:  Concentrations  of  chlordanes  in  sediments  from  the  Baltic  and  North  Sea  (ECNI-MS)  at
selected  sampling  sites  in  2001-2004  124
Figure  24:  Structures  of  Chlorpyrifos-ethyl  (A),  -methyl  (B)  and  their  main  metabolite  3,5,6-Trichloro-2-pyridinol
  (TCPy)  (C)  152
Figure  25:  Structures  of  dicofol  (A)  and  its  main  metabolite  4,4’-dichlorobenzophenone  (B)  155
Figure  26:  Structures  of  endosulfan  I  or  a  (A)  and  endosulfan  II  or  p  (B)  158
Figure  27:  Structure  of  Pentachlorophenol  160
Figure  28:  Structure  of  Trifluralin  162
Figure  29:  Typical  GC-NCTMS  traces  of  trifluralin,  chlorpyrifos-ethyl,  and  endosulfan  I  for  standard
solutions  and  real  samples  (Retention  times  may  differ  because  analysis  occurred  over  a  long
time  period)  167
Figure  30:  Overall  scheme  for  the  analysis  of  sea  water  for  chlorpyrifos,  endosulfan,  and  trifluralin  168
Figure  31:  Overall  scheme  for  the  analysis  of  sediments  for  chlorpyrifos,  endosulfan,  and  trifluralin...  169
Figure  32:  Overall  scheme  for  the  analysis  of  biota  samples  for  chlorpyrifos,  endosulfan,  and  trifluralin

170
Figure  33:  Overall  scheme  for  the  analysis  of  sea  water  for  PCP  and  TCPy  172
Figure  34:  Calibration  curves  of  chlorpyrifos,  endosulfan,  and  trifluralin  174
Figure  35:  Chlorpyrifos  concentrations  [pg/F]  in  surface  water  (5  m)  in  the  North  Sea  (July  2004)  and
Baltic  Sea  (June  2004)  182
Figure  36:  Chlorpyrifos-ethyl  concentrations  [pg/F]  in  surface  water  (5  m)  in  2003  183
Figure  37  :  Chlorpyrifos-ethyl  concentrations  [ng/kg]  in  surface  sediments  (0-2  cm)  184
Figure  38:  Concentrations  of  chlorpyrifos-ethyl  in  fish  liver;  upper  fig.  in  ¡jg/kg  wet  weight,  lower  fig.  in
pg/kg  lipid  186
Figure  39:  Summary  of  chlorpyrifos-ethyl  concentrations  in  different  marine  matrices;  min  -  max  range
and  median  values  187
Figure  40:  Endosulfan  concentrations  [pg/F]  in  surface  water  (5  m)  in  the  North  Sea  (July  2004)  and
Baltic  Sea  (June  2004)  192
Figure  41:  Endosulfan  I  concentrations  [pg/F]  in  surface  water  (5  m)  in  2003  193
Figure  42:  Endosulfan  I  concentrations  [ng/kg  dw]  in  surface  sediments  (0-2  cm)  194
Figure  43:  Concentrations  of  endosulfan  I  in  fish  liver;  upper  fig.  in  pg/kg  wet  weight,  lower  fig.  in
pg/kg  lipid  weight  196
Figure  44:  Summary  of  endosulfan  I  concentrations  in  different  marine  matrices;  min  -  max  range  and
median  values  197
Figure  45:  Trifluralin  concentrations  [pg/F]  in  surface  water  (5  m)  in  the  North  Sea  (July  2004)  and
Baltic  Sea  (June  2004)  200
Figure  46:  Trifluralin  concentrations  [pg/F]  in  surface  water  (5  m)  in  2003  201
Figure  47:  Trifluralin  concentrations  [pg/F]  in  surface  water  (5  m)  in  summer  and  winter  202
Figure  48:  Trifluralin  concentrations  [ng/kg  dw]  in  surface  sediments  (0-2  cm),  single  or  median  values
according  to  Table  97  203
Figure  49:  Trifluralin  concentrations  in  fish  liver;  upper  Fig.  in  pg/kg  wet  weight,  lower  Fig.  in  pg/kg
lipid  weight  204
Figure  50:  Summary  of  trifluralin  concentrations  in  different  marine  matrices;  min  -  max  range  and
median  values  205
Figure  51:  Degradation  of  dicofol  in  sea  water  at  room  temperature  211
Figure  52:  HPFC-MS  Chromatogram  (SIM)  of  a  standard  solution  of  TCPy  and  PCP  221
            
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