Evolution of Mg/Ca and Sr/Ca ratios during the experimental dissolution of limestone
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F19%3A73598584" target="_blank" >RIV/61989592:15310/19:73598584 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216224:14310/19:00109975
Výsledek na webu
<a href="https://www.sciencedirect.com/science/article/pii/S0009254119302840" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0009254119302840</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.chemgeo.2019.05.040" target="_blank" >10.1016/j.chemgeo.2019.05.040</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Evolution of Mg/Ca and Sr/Ca ratios during the experimental dissolution of limestone
Popis výsledku v původním jazyce
Magnesium (Mg) and strontium (Sr) preserved in speleothems are among the terrestrial climatic proxies. The mechanism of their release from impurities in limestone bedrock is usually neglected in paleoclimatic studies mainly because it is not very well understood; most cation release studies focus on pure minerals instead of limestone. Therefore, the Mg and Sr released from six types of limestone from the Moravian Karst (Czech Republic) were studied experimentally and compared with the dripwater data coming from the Punkva Caves (Moravian Karst) formed in two of the studied limestone types. The dissolution data were used to calibrate a kinetic dissolution model. The results show an incongruent dissolution of Mg-calcite and dolomite, pronounced especially in advanced stages of the dissolution. According to the results, the trace element ratios in solution were dependent mainly on (1) the limestone composition (i.e., the Mg-calcite and dolomite availability and the stoichiometry of individual minerals) and (2) on the extent of limestone-solution interaction (controlled by dissolution dynamics). Modeling indicated that the dynamics depend on the ratios of the area of rock–water and air–water interfaces to the water volume. Moreover, modeling suggests that the dynamics and subsequently also the trace element ratios are influenced by (a) the fresh surface dissolution during the initial stages of interaction and by (b) the preferential release of trace elements from mineral surfaces (nonstoichiometric dissolution). The effects of disturbed surfaces and preferential leaching are limited by available fresh surfaces. Fresh surfaces are formed through rock crushing, e.g., during physical weathering (in the field) or sample preparation (in a laboratory). The dripwaters from Punkva Caves had trace element ratios with values between the ratios resulting from the experimental dissolution of the limestones present on the site, indicating a naturally mixed composition of waters. This study has shown that Mg/Ca and Sr/Ca ratios in dripwaters might be controlled by various climate-independent variables, which raises further questions about utilizing the ratios as paleoclimatic proxies.
Název v anglickém jazyce
Evolution of Mg/Ca and Sr/Ca ratios during the experimental dissolution of limestone
Popis výsledku anglicky
Magnesium (Mg) and strontium (Sr) preserved in speleothems are among the terrestrial climatic proxies. The mechanism of their release from impurities in limestone bedrock is usually neglected in paleoclimatic studies mainly because it is not very well understood; most cation release studies focus on pure minerals instead of limestone. Therefore, the Mg and Sr released from six types of limestone from the Moravian Karst (Czech Republic) were studied experimentally and compared with the dripwater data coming from the Punkva Caves (Moravian Karst) formed in two of the studied limestone types. The dissolution data were used to calibrate a kinetic dissolution model. The results show an incongruent dissolution of Mg-calcite and dolomite, pronounced especially in advanced stages of the dissolution. According to the results, the trace element ratios in solution were dependent mainly on (1) the limestone composition (i.e., the Mg-calcite and dolomite availability and the stoichiometry of individual minerals) and (2) on the extent of limestone-solution interaction (controlled by dissolution dynamics). Modeling indicated that the dynamics depend on the ratios of the area of rock–water and air–water interfaces to the water volume. Moreover, modeling suggests that the dynamics and subsequently also the trace element ratios are influenced by (a) the fresh surface dissolution during the initial stages of interaction and by (b) the preferential release of trace elements from mineral surfaces (nonstoichiometric dissolution). The effects of disturbed surfaces and preferential leaching are limited by available fresh surfaces. Fresh surfaces are formed through rock crushing, e.g., during physical weathering (in the field) or sample preparation (in a laboratory). The dripwaters from Punkva Caves had trace element ratios with values between the ratios resulting from the experimental dissolution of the limestones present on the site, indicating a naturally mixed composition of waters. This study has shown that Mg/Ca and Sr/Ca ratios in dripwaters might be controlled by various climate-independent variables, which raises further questions about utilizing the ratios as paleoclimatic proxies.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10504 - Mineralogy
Návaznosti výsledku
Projekt
—
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2019
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
CHEMICAL GEOLOGY
ISSN
0009-2541
e-ISSN
—
Svazek periodika
523
Číslo periodika v rámci svazku
SEP
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
14
Strana od-do
107-120
Kód UT WoS článku
000480333200010
EID výsledku v databázi Scopus
2-s2.0-85067694248