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A contribution to IUGS/IAGC Global Geochemical Baselines

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DISTRIBUTION OF ELEMENTS IN STREAM SEDIMENT

by W. De Vos1, M.J. Batista2, S. Pirc3, P.J. O’Connor4, A. Demetriades5, T. Tarvainen6, R. Salminen6, S. Reeder7, I. Salpeteur8, V. Gregorauskiene9

with contributions by

K. Lax10, J. Halamic11, A. Pasieczna12, I. Slaninka13, A. Mazreku14, U. Siewers15 , M. Birke15, N. Breward7, M. Bidovec16, B. De Vivo17, A. Lima17, M. Duris18, J. Locutura19, A. Bel-lan19

1Geological Survey of Belgium, Brussels, Belgium;
2Geological Survey of Portugal, Alfragide, Portugal;
3Geology Department, University of Ljubljana, Ljubljana, Slovenia;
4Geological Survey of Ireland, Dublin, Ireland;
5Institute of Geology and Mineral Exploration, Athens, Greece;
6Geological Survey of Finland, Espoo, Finland;
7British Geological Survey, Keyworth, Nottingham, United Kingdom;
8Geological Survey of France, Orléans Cedex, France;
9Geological Survey of Lithuania, Vilnius, Lithuania;
10Geological Survey of Sweden, Uppsala, Sweden;
11Institute of Geology, Croatia, Zagreb, Croatia;
12Polish Geological Institute, Warsaw, Poland;
13Geological Survey of Slovak Republic, Bratislava, Slovak Republic;
14Centre of Civil Geology, Tirana Albania;
15Bundesanstalt für Geowissenschaften und Rohstoffe, Hannover, Germany;
16Geological Survey of Slovenia, Slovenia;
17Dipartimento di Scienze della Terra, Universita' di Napoli "Federico II", Naples, Italy;
18Czech Geological Survey, Prague, Czech Republic;
19Geological Survey of Spain, Madrid, Spain.

Stream sediment is derived from the erosion and transport of soil and rock debris, and other materials within the catchment basin upstream of the sampling site. It is, thus, representative of the geochemistry of materials from the upstream drainage basin. Stream sediment was first used effectively in mineral exploration since the 1950’s (Lovering et al. 1950, Hawkes and Bloom 1956, Boyle 1958, Webb 1958a, 1958b). Its suitability in environmental and multidisciplinary studies was recognised with the publication of the first regional geochemical atlases by the Applied Geochemistry Research Group at Imperial College of Science and Technology of the University of London (Webb et al. 1973, 1978). Since then many national geochemical atlases have been published in Europe using stream sediment (Plant and Ridgeway 1990, Plant et al. 1996, 1997). Low sample density geochemical mapping projects using stream sediment, covering large areas, were performed by Garrett and Nichol (1967), Armour-Brown and Nichol (1970), Reedman and Gould (1970), Reedman (1973), Shacklette and Boerngen (1984). An excellent review of stream sediment case studies is given by Hale and Plant (1994).

Stream sediment samples in the present FOREGS project were collected from the small catchment basin (<100 km2), where stream water and residual soil were taken (Salminen et al. 2005a). Generally, recent active stream sediment from the stream bed was sampled, except in some dry streams in Mediterranean countries, where old stream sediment was collected.

It is noted that the description below refers to the new stream sediment maps in this volume, including the results from Sweden, and not to the maps in Part 1 of the Geochemical Atlas of Europe (Salminen et al. 2005).

In the description of element distribution in stream sediment, as for soil, the following definitions were adopted with reference to the coloured maps and the histograms in Part 1 of the Geochemical Atlas of Europe (Salminen et al. 2005):

  • ·Low values group the three lowest shades of blue in the colour scale, corresponding to the range from the minimum value up to the 25th percentile, defined as “very low” and “low background” concentrations in Part 1 (Tarvainen et al. 2005, p.97), and
  • ·High values group the three highest shades of red in the colour scale, corresponding to the range of values from the 75th percentile up to the maximum, defined as “high”, “very high” and “highly anomalous” concentrations in Part 1 (Tarvainen et al. 2005, p.97).

Correlation coefficients were calculated with Pearson’s product-moment linear correlation method (Table in electronic format on website) after deletion of outliers and subsequent pairwise deletion of absent data. For a given element (or oxide), outliers were defined here as values exceeding by a factor of 1.5 other nearby results, when all analytical results are ranked. They are generally visible on the histogram accompanying each map in Part 1 of the Geochemical Atlas. A maximum of four outliers were removed in this work for the calculation of linear correlation coefficients. A list of outliers is given for stream sediment (Table 5).

Table 5. Outliers of the stream sediment data. Criterion: an outlier has a value exceeding by factor of 1.5 other nearby results, when all analytical results are ranked. A maximum of four outliers were removed for the calculation of linear correlation coefficients.

2
Sample Country Element Unit Value Next value Factor
N32W02S5 France As mg kg-1 241 122 1.98
N27E05S1 Italy Ba mg kg-1 5 000
N37W02S4 UK Ba mg kg-1 3 606 2 383 1.51
N27E05S1 Italy Cd mg kg-1 43.1
N26E14S3 Greece Cd mg kg-1 15.8
N34E07S1CZ Czech Cd mg kg-1 13.8
N34E07S4 Czech Cd mg kg-1 11.5 4.30 2.68
N34E04S1 Germany Co mg kg-1 216.0 106 2.04
N26E14S5 Greece Cr mg kg-1 3 324
N26E14S2 Greece Cr mg kg-1 2 786
N31E05S1 Italy Cr mg kg-1 2 200.00 1 267 1.74
N31E06S3 Italy Cu mg kg-1 877
N33E11S2 Slovakia Cu mg kg-1 304
N26E14S3 Greece Cu mg kg-1 220 108 2.04
N30E02S3 France Dy mg kg-1 78.2 51.9 1.50
N30E02S3 France Er mg kg-1 46.0 26.3 1.75
N36E05S1 Germany Hf mg kg-1 174 116 1.51
N27E05S1 Italy Hg mg kg-1 13.6 1.29 10.57
N30E02S3 France Ho mg kg-1 16.6 9.46 1.76
N30E02S3 France Lu mg kg-1 6.04 3.65 1.65
N37W03S1 UK MnO % 2.37 0.99 2.39
N44E06S1 Sweden Mo mg kg-1 117
N45E07S3 Sweden Mo mg kg-1 82.3
N40E03S4 Norway Mo mg kg-1 42.6
N42E05S4 Sweden Mo mg kg-1 27.9 17.0 1.64
N19W10S1 Spain Nb mg kg-1 281
N31E01S5 France Nb mg kg-1 127
N40E04S4 Norway Nb mg kg-1 122 62.0 1.97
N26E14S2 Greece Ni mg kg-1 1 406
N31E05S1 Italy Ni mg kg-1 1 033
N27E12S1 Greece Ni mg kg-1 908
N30E05S4 Italy Ni mg kg-1 680 415 1.64
N35E01S2 UK P2O5 % 2.47
N35E08S3 Poland P2O5 % 2.42 1.23 1.97
N27E05S1 Italy Pb mg kg-1 5 758
N26E14S3 Greece Pb mg kg-1 1 484
N37W04S5 Ireland Pb mg kg-1 694
N42E10S1 Finland Pb mg kg-1 681 421 1.6
N35E01S1 UK S mg kg-1 33 495
N32W02S5 France S mg kg-1 17 294 10 505 1.65
N37W04S5 Ireland Sb mg kg-1 34.1 16.8 2.03
N28W05S1 Portugal Sn mg kg-1 188
N34W02S3 UK Sn mg kg-1 175 115 1.52
N28W05S1 Portugal Ta mg kg-1 58.4
N19W10S1 Spain Ta mg kg-1 20.2 9.17 2.20
N31E01S5 France TiO2 % 4.99 3.15 1.58
N26E14S3 Greece Tl mg kg-1 7.90
N31E07S1 Italy Tl mg kg-1 5.62 2.89 1.94
N30E02S3 France Tm mg kg-1 6.43 3.65 1.76
N46E08S4 Finland TOC % 34.5 21.8 1.58
N41E06S2 Sweden U mg kg-1 98.0 59.0 1.66
N30E02S3 France Y mg kg-1 425 257 1.66
N30E02S3 France Yb mg kg-1 42.8 23.9 1.79
N27E05S1 Italy Zn mg kg-1 13 866
N26E14S3 Greece Zn mg kg-1 10 000
N34E07S4 Czech Zn mg kg-1 1 513 916 1.65
N36E05S1 Germany Zr mg kg-1 9 942 4 865 2.04

Throughout the text the following notation is used for the correlation coefficients:

  • Very strong correlation: >0.8;
  • Strong correlation: between 0.6 and 0.8;
  • Good correlation: between 0.4 and 0.6, and
  • Weak correlation: between 0.3 and 0.4.

Because of the large number of samples, even the so-called weak correlations are significant at the 0.01 confidence level.

For a discussion on the merits of correlation coefficients in this large dataset, the reader is referred to the introduction to the distribution of elements in soil.

Acknowledgements

Dr Clemens Reimann from the Geological Survey of Norway gave valuable comments on this chapter.

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