scholarly journals Contrasting Transit Times and Water-rock Interaction in Australian Upland Catchments Draining Peatland and Eucalypt Forest

2017 ◽  
Vol 17 ◽  
pp. 140-143 ◽  
Author(s):  
Ian Cartwright ◽  
Uwe Morgenstern
2016 ◽  
Vol 20 (12) ◽  
pp. 4757-4773 ◽  
Author(s):  
Ian Cartwright ◽  
Uwe Morgenstern

Abstract. Peatlands are a distinctive and important component of many upland regions that commonly contain distinctive flora and fauna which are different from those of adjacent forests and grasslands. Peatlands also represent a significant long-term store of organic carbon. While their environmental importance has long since been recognised, water transit times within peatlands are not well understood. This study uses tritium (3H) to estimate the mean transit times of water from peatlands and from adjacent gullies that contain eucalypt forests in the Victorian Alps (Australia). The 3H activities of the peatland water range from 2.7 to 3.3 tritium units (TUs), which overlap the measured (2.9 to 3.0 TU) and expected (2.8 to 3.2 TU) average 3H activities of rainfall in this region. Even accounting for seasonal recharge by rainfall with higher 3H activities, the mean transit times of the peatland waters are < 6.5 years and may be less than 2 years. Water from adjacent eucalypt forest streams has 3H activities of 1.6 to 2.1 TU, implying much longer mean transit times of 5 to 29 years. Cation ∕ Cl and Si ∕ Cl ratios are higher in the eucalypt forest streams than the peatland waters and both of these water stores have higher cation ∕ Cl and Si ∕ Cl ratios than rainfall. The major ion geochemistry reflects the degree of silicate weathering in these catchments that is controlled by both transit times and aquifer lithology. The short transit times imply that, unlike the eucalypt forests, the peatlands do not represent a long-lived store of water for the local river systems. Additionally, the peatlands are susceptible to drying out during drought, which renders them vulnerable to damage by the periodic bushfires that occur in this region.


2020 ◽  
Author(s):  
Marie Haut-Labourdette ◽  
◽  
Daniele Pinti ◽  
André Poirier ◽  
Marion Saby ◽  
...  

2021 ◽  
Vol 3 (7) ◽  
Author(s):  
Otman EL Mountassir ◽  
Mohammed Bahir ◽  
Driss Ouazar ◽  
Abdelghani Chehbouni ◽  
Paula M. Carreira

AbstractThe city of Essaouira is located along the north-west coast of Morocco, where groundwater is the main source of drinking, domestic and agricultural water. In recent decades, the salinity of groundwater has increased, which is why geochemical techniques and environmental isotopes have been used to determine the main sources of groundwater recharge and salinization. The hydrochemical study shows that for the years 1995, 2007, 2016 and 2019, the chemical composition of groundwater in the study area consists of HCO3–Ca–Mg, Cl–Ca–Mg, SO4–Ca and Cl–Na chemical facies. The results show that from 1995 to 2019, electrical conductivity increased and that could be explained by a decrease in annual rainfall in relation to climate change and water–rock interaction processes. Geochemical and environmental isotope data show that the main geochemical mechanisms controlling the hydrochemical evolution of groundwater in the Cenomanian–Turonian aquifer are the water–rock interaction and the cation exchange process. The diagram of δ2H = 8 * δ18O + 10 shows that the isotopic contents are close or above to the Global Meteoric Water Line, which suggests that the aquifer is recharged by precipitation of Atlantic origin. In conclusion, groundwater withdrawal should be well controlled to prevent groundwater salinization and further intrusion of seawater due to the lack of annual groundwater recharge in the Essaouira region.


Author(s):  
Carleton R. Bern ◽  
Justin E. Birdwell ◽  
Aaron M. Jubb

Comparisons of hydrocarbon-produced waters from multiple basins and experiments using multiple shales illustrate water–rock interaction influence on produced water chemistry.


1990 ◽  
Vol 84 (1-4) ◽  
pp. 322-325 ◽  
Author(s):  
C.I. Steefel ◽  
P. Van Capellen ◽  
K.L Nagy ◽  
A.C. Lasaga

2014 ◽  
Vol 78 (6) ◽  
pp. 1473-1477
Author(s):  
Jan Přikryl ◽  
Andri Stefánsson

The interaction of CO2-rich water with olivine was studied using geochemical reaction modelling in order to gain insight into the effects of temperature, acid supply (CO2) and extent of reaction on the secondary mineralogy, water chemistry and mass transfer. Olivine (Fo93) was dissolved at 150 and 250ºC and pCO2 of 2 and 20 bar in a closed system and an open system with secondary minerals allowed to precipitate. The progressive water–rock interaction resulted in increased solution pH, with gradual carbonate formation starting at pH 5 and various Mg-OH and Mg-Si minerals becoming dominant at pH>8. The major factor determining olivine alteration is the pH of the water. In turn, the pH value is determined by acid supply, reaction progress and temperature.


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