Water contents and hydrogen isotope compositions of amphibole in aillikites from the Tarim large igneous province, NW China: Insight into Earth’s deep water cycle
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F41601670%3A_____%2F23%3AN0000008" target="_blank" >RIV/41601670:_____/23:N0000008 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216305:26110/24:PU155169 RIV/67985831:_____/24:00578533
Výsledek na webu
<a href="https://doi.org/10.1130/B36906.1" target="_blank" >https://doi.org/10.1130/B36906.1</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1130/B36906.1" target="_blank" >10.1130/B36906.1</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Water contents and hydrogen isotope compositions of amphibole in aillikites from the Tarim large igneous province, NW China: Insight into Earth’s deep water cycle
Popis výsledku v původním jazyce
Water is known to play a crucial role in the generation of many large igneous provinces (LIP) worldwide, but the amount and origin of the water in their sources is still under debate. To address this question, this paper presents in situ major-, trace-element, and Sr isotope data coupled with bulk-mineral O-HHe isotope analyses of amphibole in a suite of aillikites from the Tarim LIP (NW China). The cores of zoned macrocrysts and microcrysts display partially overlapping compositions ranging between edenite and pargasite (75–83 versus 75–80 Mg#), which suggest a common origin from an evolving magma. The rims (Mg# = 75–80) of both macrocrysts and microcrysts are very similar to their cores for many elements, except for higher Sr and Ba contents. All the amphibole zones show similar primitive mantle–normalized trace element patterns, suggesting that they crystallized at different stages during magmatic evolution. This interpretation is confirmed by the homogenous Sr isotope compositions (87Sr/86Sr(i) = 0.70298–0.70394) of these amphiboles, which overlap with those of magmatic apatites and perovskites in these aillikites. The hydrogen isotope compositions (δD = −120‰ to −140‰) of the amphiboles are significantly lower than average mantle values. Given the low water contents (<0.66 wt%) of these minerals, the low H isotope signatures of the amphiboles might be caused by variable H2O loss during magma ascent. However, open-system Rayleigh fractionation modeling suggests that the hydrogen isotope compositions of these amphibole phenocrysts cannot be fully reproduced by crystallization following magmatic degassing. These low δD values require incorporation of recycled altered oceanic crust containing hydrous components in the plume source of these aillikites, which is consistent with the previously published moderately radiogenic He isotope ratios of olivine separates and bulk-rock Os and Pb isotope data for these same samples. We conclude that water in these magmas was derived from a plume source containing recycled water-bearing oceanic crust.
Název v anglickém jazyce
Water contents and hydrogen isotope compositions of amphibole in aillikites from the Tarim large igneous province, NW China: Insight into Earth’s deep water cycle
Popis výsledku anglicky
Water is known to play a crucial role in the generation of many large igneous provinces (LIP) worldwide, but the amount and origin of the water in their sources is still under debate. To address this question, this paper presents in situ major-, trace-element, and Sr isotope data coupled with bulk-mineral O-HHe isotope analyses of amphibole in a suite of aillikites from the Tarim LIP (NW China). The cores of zoned macrocrysts and microcrysts display partially overlapping compositions ranging between edenite and pargasite (75–83 versus 75–80 Mg#), which suggest a common origin from an evolving magma. The rims (Mg# = 75–80) of both macrocrysts and microcrysts are very similar to their cores for many elements, except for higher Sr and Ba contents. All the amphibole zones show similar primitive mantle–normalized trace element patterns, suggesting that they crystallized at different stages during magmatic evolution. This interpretation is confirmed by the homogenous Sr isotope compositions (87Sr/86Sr(i) = 0.70298–0.70394) of these amphiboles, which overlap with those of magmatic apatites and perovskites in these aillikites. The hydrogen isotope compositions (δD = −120‰ to −140‰) of the amphiboles are significantly lower than average mantle values. Given the low water contents (<0.66 wt%) of these minerals, the low H isotope signatures of the amphiboles might be caused by variable H2O loss during magma ascent. However, open-system Rayleigh fractionation modeling suggests that the hydrogen isotope compositions of these amphibole phenocrysts cannot be fully reproduced by crystallization following magmatic degassing. These low δD values require incorporation of recycled altered oceanic crust containing hydrous components in the plume source of these aillikites, which is consistent with the previously published moderately radiogenic He isotope ratios of olivine separates and bulk-rock Os and Pb isotope data for these same samples. We conclude that water in these magmas was derived from a plume source containing recycled water-bearing oceanic crust.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10505 - Geology
Návaznosti výsledku
Projekt
<a href="/cs/project/GX19-29124X" target="_blank" >GX19-29124X: VÝVOJ STAVEB A GEOCHEMICKÉ SIGNATURY KARBONATITŮ V ČASE: VÝZNAM MOBILITY A KONCENTRACE KRITICKÝCH KOVŮ</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2023
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Geological Society of America Bulletin
ISSN
0016-7606
e-ISSN
1943-2674
Svazek periodika
136
Číslo periodika v rámci svazku
September 20, 2023
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
14
Strana od-do
2097-2110
Kód UT WoS článku
001236797500004
EID výsledku v databázi Scopus
—