SUBSOLIDUS DEUTERIC/HYDROTHERMAL ALTERATION OF EUDIALYTE IN LUJAVRITE FROM THE PILANSBERG ALKALINE COMPLEX, SOUTH AFRICA

dc.contributor.authorMitchell R.H.
dc.contributor.authorLiferovich R.P.
dc.date.accessioned2025-01-25T04:34:05Z
dc.date.available2025-01-25T04:34:05Z
dc.date.issued2006
dc.description.abstractThe most evolved rocks of the Pilansberg alkaline complex are aegirine lujavrites in which three varieties of eudialyte are recognized on the basis of textural relationships and composition. Manganoan eudialyte-I is a relict orthomagmatic phase occurring as poikilitic plates or as relict grains in pseudomorphed euhedral phenocrysts. Late eudialyte-II ranges in composition from manganoan eudialyte through kentbrooksite to taseqite-like varieties and is considered to be formed by cation exchange with eudialyte-I and alkaline fluids. Eudialyte-III is a hydrothermal phase replacing eudialyte-II, and has either taseqite-like (5-7.3 wt.% SrO, < 2.0 wt.% REE2O3) or kentbrooksite (< 1.5 wt.% SrO, ~ 8.5 wt.% REE2O3) compositions. Three styles of replacement of eudialyte-I and -II are recognizable. Type 1 involves replacement by complex aggregates of zircon, fergusonite-(Ce), allanite-(Ce), britholite-(Ce), titanite, pyrochlore, albite and potassium feldspar, i.e. a "miaskitic" paragenesis. Type 2 alteration consists of complex aggregates dominated by deuteric Na-Zr-silicates (?catapleiite), stronalsite, strontium-apatite and lamprophyllite replacing eudialyte-I and -II and relicts of the "miaskitic paragenesis", i.e. a highly sodic "agpaitic-to-hyperagpaitic" paragenesis. Type 3 replacement involves mantling of any residual eudialyte-II and zircon, and replacement of deuteric Na-Zr-silicates by eudialyte-III together with barytolamprophyllite as late hydrothermal phases. Further alteration and replacement resulted in the superposition of natrolite, britholite, pyrochlore, allanite and diverse Ba- and Mn-based minerals onto the types 2 and 3 assemblages, and ultimately to the deposition of allanite-(La), La-dominant REE carbonates and rarely a silica phase. All of the alteration styles are considered to have occurred in situ under subsolidus conditions (< 450 °C) by interaction of pre-existing eudialyte and other minerals with deuteric, sodium- and chlorine-bearing aqueous fluids. The evolution of the replacement products is from a miaskitic through an agpaitic to a hyperagpaitic paragenesis and ultimately back to a low agpaitic-to-miaskitic assemblage, reflecting changes in the a(Na+)/a(Cl-) ratio and alkalinity of the deuteric/hydrothermal fluids. © 2006 Elsevier B.V. All rights reserved.
dc.identifierhttps://www.elibrary.ru/item.asp?id=14497193
dc.identifier.citationLithos, 2006, 91, 1-4, 352-372
dc.identifier.doi10.1016/j.lithos.2006.03.025
dc.identifier.issn0024-4937
dc.identifier.urihttps://repository.geologyscience.ru/handle/123456789/47546
dc.subjectALTERATION
dc.subjectAUTOMETASOMATIC
dc.subjectEUDIALYTE
dc.subjectLUJAVRITE
dc.subjectPILANSBERG
dc.titleSUBSOLIDUS DEUTERIC/HYDROTHERMAL ALTERATION OF EUDIALYTE IN LUJAVRITE FROM THE PILANSBERG ALKALINE COMPLEX, SOUTH AFRICA
dc.typeСтатья

Файлы

Оригинальный пакет

Показано 1 - 1 из 1
Загрузка...
Изображение-миниатюра
Имя:
Mitc_06.pdf
Размер:
2.93 MB
Формат:
Adobe Portable Document Format

Коллекции