TY - JOUR
T1 - Li isotopes in the middle Yellow River
T2 - Seasonal variability, sources and fractionation
AU - Gou, Long Fei
AU - Jin, Zhangdong
AU - Pogge von Strandmann, Philip A.E.
AU - Li, Gen
AU - Qu, Yuan Xin
AU - Xiao, Jun
AU - Deng, Li
AU - Galy, Albert
N1 - Publisher Copyright:
© 2019 Elsevier Ltd
PY - 2019/3/1
Y1 - 2019/3/1
N2 - To evaluate the roles of climate and hydrology in continental-scale silicate weathering, we applied Li isotopes to the Yellow River and systematically investigated seasonal Li flux, Li isotopic compositions and potential sources. We collected samples from the middle reaches of the Yellow River weekly over the full hydrological year of 2013. We find that the dissolved Li is mainly derived from silicates and evaporites in the arid to semi-arid Yellow River basin. Silicate weathering of loess during the monsoonal season dominates the Li flux in the middle reaches of the Yellow River, with a positive relationship between dissolved Li flux and physical erosion rate. Evaporite contribution for riverine Li was relatively constant in the middle reaches of the Yellow River but slightly increased after the storm event, with an average proportion of ∼25%, which might represent the proportion of evaporite contribution to global oceans. Seasonal variations in the riverine Li isotopic compositions are dominantly controlled by temperature with a fractionation gradient as −0.182‰ per °C over the full year with deviations likely driven by re-dissolution of suspended particulate matter, extreme hydrological events, and groundwater contribution. Temperature dependent δ 7 Li value variation of river water inputted into oceans indicates that Cenozoic climate cooling itself may be able to explain ∼2‰ of the 9‰ rise of Cenozoic seawater δ 7 Li value (Misra and Froelich, 2012). The seasonal variation in riverine Li isotopes highlights that erosion and weathering of loess may provide valuable clues on secular chemical weathering and seawater δ 7 Li variation spanning a range of time scales.
AB - To evaluate the roles of climate and hydrology in continental-scale silicate weathering, we applied Li isotopes to the Yellow River and systematically investigated seasonal Li flux, Li isotopic compositions and potential sources. We collected samples from the middle reaches of the Yellow River weekly over the full hydrological year of 2013. We find that the dissolved Li is mainly derived from silicates and evaporites in the arid to semi-arid Yellow River basin. Silicate weathering of loess during the monsoonal season dominates the Li flux in the middle reaches of the Yellow River, with a positive relationship between dissolved Li flux and physical erosion rate. Evaporite contribution for riverine Li was relatively constant in the middle reaches of the Yellow River but slightly increased after the storm event, with an average proportion of ∼25%, which might represent the proportion of evaporite contribution to global oceans. Seasonal variations in the riverine Li isotopic compositions are dominantly controlled by temperature with a fractionation gradient as −0.182‰ per °C over the full year with deviations likely driven by re-dissolution of suspended particulate matter, extreme hydrological events, and groundwater contribution. Temperature dependent δ 7 Li value variation of river water inputted into oceans indicates that Cenozoic climate cooling itself may be able to explain ∼2‰ of the 9‰ rise of Cenozoic seawater δ 7 Li value (Misra and Froelich, 2012). The seasonal variation in riverine Li isotopes highlights that erosion and weathering of loess may provide valuable clues on secular chemical weathering and seawater δ 7 Li variation spanning a range of time scales.
KW - Li isotopes
KW - Loess weathering
KW - Seasonal variation
KW - Temperature dependency
KW - The Chinese Loess Plateau
KW - The Yellow River
UR - https://www.scopus.com/pages/publications/85060182864
U2 - 10.1016/j.gca.2019.01.007
DO - 10.1016/j.gca.2019.01.007
M3 - 文章
AN - SCOPUS:85060182864
SN - 0016-7037
VL - 248
SP - 88
EP - 108
JO - Geochimica et Cosmochimica Acta
JF - Geochimica et Cosmochimica Acta
ER -