HSE DEGASSING SYSTEM · Degassing systematics of Highly Siderophile Elements from magmas: New constrains on the convecting mantle, and the origins of global HSE anomalies in sedimentary rocks
6РП — Действия „Мария Кюри“
- Период
- 2005-02-01 → 2007-01-31
- Финансиране от ЕС
- 162 448 €
- Участници
- 1
- Схема
- EIF
Линиите свързват координатора с партньорите.
Накратко на български
Разпределението на платинови елементи (като осмий и платина) в магмите и тяхното изпаряване при изригване се анализира чрез изследване на скали от земната мантия. Това помага да се разбере дали следите от тези елементи в седиментите идват от вулкани или от метеоритни удари.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Final Activity Report Summary - HSE DEGASSING SYSTEM (Degassing systematics ...: New constrains on the convecting mantle, and the origins of global HSE anomalies in sedimentary rocks)
A detailed assessment of the geochemistry of platinum group elements (PGEs), namely osmium (Os), iridium (Ir), ruthenium (Ru), platinum (Pt) and palladium (Pd) plus rhenium (Re) was made to understand 1. the distribution of these elements in the mantle and melts; to provide an understanding of 2. the relative volatility of the PGEs; 3. the effects of degassing on PGE abundances in magmas; 4. how this might affect PGE anomalies found in sedimentary horizons, where there was a debate as to the origin of the elemental spikes, i.e. on whether they were of meteorite impact origin or large scale degassing of intense volcanic episodes. The first detailed assessment of PGE abundances in sulphides within pyroxenites was made, in an effort to try to understand the factors controlling the relative abundances of Re, Pt and Os is basaltic rocks. This showed that it was possible for magmatic rocks with highly unusual Os isotopic signatures to be generated by melting of reacted zones between peridotites, i.e. the rock type formerly thought to control the chemistry of all mantle-derived melts, and pyroxenites. Although the melting of these reacted layers creates unusual isotopic signatures because of subtle fractionation of Re/Os and Pt/Os, the abundances of these elements in the resulting melts is ultimately controlled by their solubilities in silicate melts. Hence, even though it could be shown from this study that mantle source regions for magmatic rocks were much more diverse than previously recognised, there was an underlying limit on the amount of PGEs that could enter the silicate melts. Establishing the limits and control on PGE abundances in mantle-derived melts then allowed a focus on the response to relative differences in eruption pressure on the PGE abundances of volcanic rocks. This part of the study demonstrated that Re abundances in lavas erupted under pressure, e.g. in substantial water depth or buried beneath glacial loads, contained significantly more Re than their lower pressure counterparts. However, for other PGEs, such as Pd, complications in the history of the mantle source region provided an over-riding control, as for example in the Philippine Sea Plate basalts, and degassing effects were minimal. No significant differences were so far observed for Pt, Ru, Os or Ir that could be attributed to differences in volatility during eruption. The main implication of the results was that there was very little evidence that volatile emissions of any of the PGEs could be the main cause of elemental anomalies in sediment sequences, therefore so other mechanisms such as meteorite impacts appeared as more likely explanations.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
Highly Siderophile Element (HSE: Os, Ir, Ru, Rh, Pt, Pd, Au & Re) studies in oceanic basalts provide vital information on the partial melting regime, constrains on the different mantle end-member compositions, and hence on mantle geodynamics. However, it has been recently showed that Re could be lost by volatilisation upon eruption of the basalts. For the other HSE, the only evidence (indirect) of their potential losses via degassing resides in the high Ir and Au contents of volcanic emissions and airborne particles.This project aims to obtain quantitative constrains on the volatile loss of HSE during magma degassing in order to better constrain the mantle composition, the degassing flux of HSE to atmosphere and determine whether global HSE anomalies in the sedimentary record result from meteorite impacts or large-scale volcanic emissions. These objectives will be achieved by coupling studies of HSE and volatile elements in oceanic basalts from the Lau Basin, Iceland and the East Pacific Rise. Analyses o f melt inclusions and basalt glasses will provide the pre-eruptive and post-eruptive composition of the lavas.HSE will be determined by ultra-sensitive inductively coupled plasma mass spectrometry (ICP-MS) after ultra-low blank separation techniques. Volatile elements (CO2, H2O, d13C and d18O) will be analysed using a volatile extraction line coupled with ICP-MS, secondary ion mass spectrometry and Fourier transform Infra-Red Spectroscopy. This project will promote research excellence and the innovative and multidisciplinary aspect of European research by undertaking the first study ever done on the effects of degassing on HSE systematics.The development of new, ultra-low blank HSE separation coupled with for the first time micro-drilling techniques applied to the analysis of HSE will advance analytical techniques in HSE chemistry, directly applicable for other low-level HSE geochemical studies of the Earth, environmental and medical (anti-cancer drugs) sciences.
Оригинален текст от CORDIS (на английски).
Участници
- UNIVERSITY OF DURHAM · DURHAMКоординаторОбединеното кралство
Връзки
Данни: CORDIS, © Европейски съюз
