PERIDOTITE CLINOPYROXENE CHEMISTRY REFLECTS MANTLE PROCESSES RATHER THAN CONTINENTAL VERSUS OCEANIC SETTINGS

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dc.contributor.author Rivalenti G.
dc.contributor.author Vannucci R.
dc.contributor.author Rampone E.
dc.contributor.author Mazzucchelli M.
dc.contributor.author Piccardo G.B.
dc.contributor.author Piccirillo E.M.
dc.contributor.author Bottazzi P.
dc.contributor.author Ottolini L.
dc.date.accessioned 2020-11-21T02:35:05Z
dc.date.available 2020-11-21T02:35:05Z
dc.date.issued 1996
dc.identifier https://elibrary.ru/item.asp?id=487594
dc.identifier.citation Earth and Planetary Science Letters, 1996, , 3, 423-437
dc.identifier.issn 0012-821X
dc.identifier.uri https://repository.geologyscience.ru/handle/123456789/19181
dc.description.abstract Comparison of 360 trace element analyses of clinopyroxenes from peridotites indicates that clinopyroxene composition cannot discriminate between suboceanic and subcontinental mantle. Clinopyroxenes from abyssal and fore-arc peridotites have the lowest incompatible element concentrations and record melting and basalt extraction as the dominant process. Clinopyroxenes from continental peridotite massifs partially overlap the composition of clinopyroxenes from abyssal peridotites and, in general, behave as a less depleted component in the chemical variation trends defined by the latter. In the peridotite massifs, subsolidus re-equilibration involving phase transitions (spinel to plagioclase facies) may cause significant element variations in clinopyroxene (e.g. Sr and Eu/Eu* decrease, REE, Ti increase). Metasomatic processes cause only comparatively minor trace element variations.Clinopyroxenes from mantle xenoliths in OIB and continental alkali basalts have the highest incompatible trace element concentrations and the largest compositional variations. They primarily record metasomatic enrichment processes, which are similar in suboceanic and subcontinental mantle. These processes induced the highest incompatible element enrichment in the clinopyroxenes from the most refractory peridotites, supporting the chromatographic nature of infiltration metasomatism. This enrichment, however, does not affect Ti, which is in the same concentration range in clinopyroxenes from both xenoliths and abyssal peridotites. The apparent Ti immobility may be due to several causes, such as reduced Ti solubility in hydrous fluids, fractionation of Ti-rich phases from percolating silicate melts, reaction with carbonatite melts formerly equilibrated with amphibole-peridotite. In general, clinopyroxene geochemistry does not allow a clear distinction between different metasomatic agents.The similarity between the geochemical characteristics of xenoliths from continental and oceanic environments supports previous results that the compositions of the pre-metasomatic lithosphere and of the asthenosphere, from where metasomatic agents derive, do not differ in the two environments.
dc.subject PERIDOTITES
dc.subject CLINOPYROXENE
dc.subject MANTLE
dc.subject TRACE-ELEMENT ANALYSES
dc.subject MINOR-ELEMENT ANALYSES
dc.subject METASOMATISM
dc.title PERIDOTITE CLINOPYROXENE CHEMISTRY REFLECTS MANTLE PROCESSES RATHER THAN CONTINENTAL VERSUS OCEANIC SETTINGS
dc.type Статья


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