Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-28T16:03:28.907Z Has data issue: false hasContentIssue false

The geochemistry of the Rhine and the Rhone. 5, Synthesisand conclusions

Published online by Cambridge University Press:  15 August 2009

H. L. Golterman*
Affiliation:
Station Biologique de la Tour du Valat, le Sambuc, 13200 ARLES
Get access

Abstract

Every month 2 samples of the Rhine and 1 sample of the Rhone are analysed for about 20 chemical and physical variables at 7 stations by two monitoring agencies.This paper presents some of our conclusions on the accuracy of these programmes and on the solubility of the calcium/carbonate/sulphate/phosphate system. In total we have analysed 916 data sets ; they were screened for imprecision before being used.At all stations the water is saturated with CaCO3 , but the "apparent" solubility product depends on the pH. The regression line can be described by IPca = 8.73 x 10-15. pH15.667.In both the Rhine and the Rhone an acidification is seen and an increase of the sulphate concentration when going downstream. We have shown that the increase in sulphate concentration is due to the disposal of CaSO4. This addition of sulphate influences the quotient Ca/HCO3. The data fit very well the theoretical regression line Ca/HCO3 = 0,5(SO4) + 0.5.The acidification originates from the mineralization of organic matter. For 6 stations dowstream from the great lakeswe found that the two rivers are saturated with hydroxy-apatite, the -log of the ionic product being 49.9 (Rhine ; σ = 0.6 ;N = 259) and 50.0 (Rhone ; σ = 0.3 ; N = 479). The o-phosphate concentration does not therefore depend on the phosphate loading of the rivers, but on the Ca concentration, the temperature and the pH. This has great influence on the transport of phosphate through the delta's of the two rivers. The disturbance of acidity and buffering capacity influences heavy metal behaviour as well.

Type
Research Article
Copyright
© Masson, 1985

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)