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- MakaleAçık Erişim2016Scopus SJRQ1Complex subvolcanic magma plumbing system of an alkali basaltic maar-diatreme volcano (Elie Ness, Fife, Scotland)
Gernon, T. M.; Upton, B. G. J.; Ugra, R.; Yücel, C.; Taylor, R. N.; Elliott, H.
Alkali basaltic diatremes such as Elie Ness (Fife, Scotland) expose a range of volcanic lithofacies that points to a complex, multi -stage emplacement history. Here, basanites contain phenocrysts including pyrope garnet and sub-calcic augites from depths of similar to 60 km. Volcanic rocks from all units, pyroclastic and hypabyssal, are characterised by rare earth element (REE) patterns that show continuous enrichment from heavy REE (HREE) to light REE (LREE), and high Zr/Y that are consistent with retention of garnet in the mantle source during melting of peridotite in a garnet lherzolite fades. Erupted garnets are euhedral and unresorbed, signifying rapid ascent through the lithosphere. The magmas also transported abundant pyroxenitic clasts, cognate with the basanite host, from shallower depths (similar to 35-40 km). These clasts exhibit wide variation in texture, mode and mineralogy, consistent with growth from a range of compositionally diverse melts. Further, clinopyroxene phenocrysts from both the hypabyssal and pyroclastic units exhibit a very wide compositional range, indicative of polybaric fractionation and magma mixing. This is attributed to stalling of earlier magmas in the lower crust principally from similar to 22 to 28 km as indicated by pyroxene thermobarometry. Many clinopyroxenes display chemical zoning profiles, occasionally with mantles and rims of higher magnesium number (Mg#) suggesting the magmas were mobilised by juvenile basanite magma. The tuffs also contain alkali feldspar megacrysts together with Feclinopyroxene, zircon and related salic xenoliths, of the 'anorthoclasite suite' - inferred to have crystallised at upper mantle to lower crustal depths from salic magma in advance of the mafic host magmas. Despite evidence for entrainment of heterogeneous crystal mushes, the rapidly ascending melts experienced negligible crustal contamination. The complex association of phenocrysts, megacrysts and autoliths at Elie Ness indicates thorough mixing in a dynamic system immediately prior to explosive diatreme-forming eruptions. (C) 2016 Elsevier B.V. All rights reserved.
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İncele - MakaleYalnız künye2009Scopus SJRQ1C2/c pyroxene phenocrysts from three potassic series in the Neogene alkaline volcanics, NE Turkey: Their crystal chemistry with petrogenetic significance as an indicator of P -T conditions
Aydin, Faruk; Thompson, Richard M.; Karsli, Orhan; Uchida, Hinako; Burt, Jason B.; Downs, Robert T.
Chemical and structural data are reported for C2/c pyroxene phenocrysts collected from three potassic series (Group A: basanite-tephrite, Group B: tephrite-phonolitic tephrite, Group C: alkaline basalt-trachybasalt) of the Neogene alkaline volcanics (NAVs) in northeastern Turkey, in order to investigate the evolution of the magmatic plumbing system and the location of magma chamber(s) with crystallization conditions. The rock series hosting the clinopyroxene phenocrysts show generally porphyritic texture and have a variable phenocryst-rich nature (20-58%), with phenocryst assemblages characterized by cpx ± ol ± plag ± foid ± amp ± bio. The clinopyroxene phenocrysts can be chemically classified as Ti- and Fe3-rich Al-diopsides for Groups A and B (ABcpxs) and Ti- and Fe3-poor Al-diopsides for Group C (Ccpxs). They have poorly variable composition, clustering in the diopside field. Structurally, the diopside groups have nearly similar a (ranging from 9.73 to 9.75 Å), Vcell (437.2-440.9 Å3), and hbetai angle values (106.01°-106.23°), but some differences in polyhedral parameters and geometries of the AB-cpxs and C-cpxs have been observed. For example, the AB-cpxs are characterized by. larger c (5.27-5.30 vs. 5.25-5.28 Å), VT (2.27-2.30 vs. 2.23-2.28 Å3), and VM2 (25.53-25.72 vs. 25.41-25.59 Å3) values and smaller b (8.87-8.88 vs. 8.88-8.91 Å) and VM1(11.49-1.63 vs. 11.64-11.83 Å3) values with respect to the C-cpxs. In addition, the AB-cpxs show higher values of VM2/VM1 (2.20-2.23) due to large VM2 and small VM1 compared to the VM2/ VM1 ratios of the C-cpxs (<2.19). Such differences in the crystal structure of the AB-cpxs and C-cpxs from the NAVs are partly related to different crystallization pressures, but mostly related to variation in melt composition and, possibly, the influence of other crystallizing mineral phases. In particular, R(M2-O1) and R(M1-O2) (i.e. bond lengths) differences in the clinopyroxenes of different groups support the presence of evolved host rocks with different alkaline character (i.e. silicaundersaturated Groups A-B and silica-saturated Group C). Based on the cpx-geothermobarometry, the crystallization pressures for the C-cpxs are lower than 4.5 kbars, but the AB-cpxs have relatively high-pressure values (5.6- 10.6 kbars), suggesting that the AB-cpxs crystallized in higher pressure environments. The relatively higher crystallization temperatures of the AB-cpxs also indicate higher cooling rates. The P-T estimates suggest that the source regions of the clinopyroxene phenocrysts from the NAVs were crustal magma chambers in a closed plumbing system at a moderate- to low-pressure regime.
AtıfScopus25WoS27OpenAlex28İncele - MakaleAçık Erişim2009Scopus SJRQ1Compositional variations, zoning types and petrogenetic implications of low-pressure clinopyroxenes in the neogene alkaline volcanic rocks of northeastern Turkey
Aydin, Faruk; Karsli, Orhan; Sadiklar, M. Burhan
Clinopyroxene phenocrysts and microphenocrysts in different series of the Neogene alkaline volcanic rocks from the eastern Pontides (NE Turkey) record various stages in the crystallization conditions and evolution history of the alkaline melt as well as its origin. Crystal chemical studies reveal that the clinopyroxenes in each rock series show strong textural and compositional similarities, which all reflect a common petrogenetic affinity. They have relatively high Mg-numbers (0.68-0.95), variable Al2O3 (1.3-9.6 wt%), low TiO2 (<2.7 wt%) and Na2O (<0.9 wt%) contents and low Al[6]/Al[4] ratios (mostly <0.25), suggesting relatively low-pressure crystallization conditions of the magma in the storage region. The pressures calculated for the clinopyroxenes in each series are nearly similar and vary in the range of 2.4-4.6 ± 0.9 kbars, which approximately corresponds to a crystallization depth of 7-14 ± 3 km. The analyses of the compositional trends of the clinopyroxenes indicate the following types of zoning: (i) oscillatory and sectorial zoning related to melt crystallization (i.e. rapid cooling and crystallization), (ii) oscillatory, reverse zoning related to the different crystallization paths under a variable fluid regime, (iii) normal zoning related to the differentiation and fractional crystallization of the magma. Based on the primitive mantle- and chondrite-normalized trace and rare earth element patterns, all clinopyroxenes have high abundances of incompatible elements (i.e. La, Ce) with negative high field strength element anomalies (i.e. Zr, Ti) and low Nb/Y (0.1-0.2), Th/Y (< 0.1) and Rb/Y (< 0.03) ratios, suggesting derivation from a similar source. Obtained textural and mineral chemical data, as well as whole-rock compositions, thus suggest that the clinopyroxenes may have started to crystallize from alkaline basaltic magma derived from a homogeneous lithospheric mantle enriched by an earlier subduction event. After this process, the alkaline magma, from which early clinopyroxenes crystallized, underwent a relatively low-pressure fractional crystallization process. This was in closed magma chambers at different levels of the crust (or within a volcanic conduit system devoid of interaction processes), shown by variations in the different crystallization paths and in the fluid regime of the melt during differentiation and ascent of the magma, in a post-collisional extensional tectonic regime which affected the eastern Pontides during the Neogene.
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