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1.
Peralkaline silicate lavas at Oldoinyo Lengai, Tanzania 总被引：1，自引：0，他引：1
A detailed study of Oldoinyo Lengai has led to the recognition of two major cone-building stages. An early, predominantly phonolitic stage, Lengai I, forms the southern cone. The recent nephelinitic Lengai II developed following a major sector collapse event over Lengai I. Petrography of Lengai II lavas show that nephelinite is combeite- and wollastonite-bearing. All Oldoinyo Lengai lavas are peralkaline and highly evolved in terms of low Mg#, Ni and Cr values. Within the unique Lengai II combeite–wollastonite–nephelinite (CWN) peralkalinity increases with time to extreme values (Na + K)/Al = 2.36. Mineralogical expression of peralkalinity is the presence of combeite and Na-rich clinopyroxene. In addition, exceptionally high Fe2O3 (up to 10.28 wt.%) in nepheline is an indicator for alumina deficiency. Combeite also shows high Fe3+. Phonolite and CWN of Lengai I and Lengai II show similarly enriched LILE and LREE values and generally parallel patterns in PM normalized and REE plots. 相似文献
2.
Carbonatite Magmatism and Plume Activity: Implications from the Nd, Pb and Sr Isotope Systematics of Oldoinyo Lengai 总被引：19，自引：3，他引：16
New Nd (0.51261–0.51268), Pb (206Pb/204Pb: 19.24–19.26),and Sr (0.70437–0.70446) isotopic compositions from tennatrocarbonatite lavas, collected in June 1993 from OldoinyoLengai, the only known active carbonatite volcano, are relativelyuniform, and are similar to data from the 1960 and 1988 flows.Three of the samples contain silicate spheroids, one of whichhas Nd and Sr isotopic ratios similar to host natrocarbonatite,consistent with an origin by liquid immiscibility or the mixingof melts with similar isotopic compositions. Pb isotope datafor two samples of trona are inconsistent with its involvementin the genesis of natrocarbonatite. New Pb isotope data fromsilicate volcanic and plutonic blocks (ijolite, nephelinite,phonolite, syenite) from Oldoinyo Lengai are highly variable(206Pb/204Pb, 17.75–19.34; 207Pb/204Pb, 15.41–15.67;208Pb/204Pb, 37.79–39.67), and define near-linear arraysin Pb-Pb diagrams. The isotopic data for the silicate rocksfrom Oldoinyo Lengai are best explained by invoking discretepartial melting events which generate undersaturated alkalinesilicate magmas with distinct isotopic ratios. Pb isotope ratiosfrom most ijolites and phonolites are predominantly lower andmore variable than from the natrocarbonatites, and are attributedto interaction between silicate melts involving HIMU and EMIsource components and an additional component, such as lower-crustalgranulites, DMM or PREMA (prevalent mantle). Variations in Nd,Pb and Sr isotope ratios from Oldoinyo Lengai, among the largestyet documented from a single volcano, are attributed to mantlesource heterogeneity involving mainly the mixing of HIMU andEMI mantle components. Based on the new isotopic data from OldoinyoLengai and data from other East African carbonatites, and mantlexenoliths, we propose a two-stage model in an attempt to explainthe isotope variations shown by carbonatites in this area. Themodel involves (I) the release of metasomatizing agents withHIMU-like signatures from upwelling mantle (‘plume’)source, which in turn metasomatize the sub-continental (old,isotopically enriched, EMI-like) lithosphere, and (2) variabledegrees and discrete partial melting of the resulting heterogeneous,metasomatized lithosphere. KEY WORDS: carbonatite; isotopes; Oldoinyo Lengai; mantle plumes
*Telephone: (613) 788–2660, ext. 4419. Fax: (613) 788–4490. e-mail: kbell{at}ccs.carleton.ca 相似文献
3.
《Journal of African Earth Sciences》2011,59(5):734-751
A 500 m sequence of horizontal lava flows forms the Gregory rift escarpment of the western rift shoulder between Lake Natron and Oldoinyo Lengai. A detailed volcanic stratigraphy of this >1.2 Ma evolution of the EAR in Northern Tanzania is presented. The sequence is formed by several distinct rock suites, with increasing alkalinity from base to top. Alkali olivine basalts of the Waterfall Sequence at the base are followed by a basanite series, and by a range of evolved nephelinites forming the upper part of the escarpment. Numerous dykes and Strombolian scoria deposits indicate local fissure eruptions as opposed to or in addition to more distant sources. Primitive compositions within each of the series indicate variable candidates for primary magmas. The composition of the basanite suite ranges from primitive mantle melts (high Mg#, Cr, Ni) to more evolved rocks, in particular hawaiites, generated by fractionation of olivine, pyroxene and magnetite. Inter-bedded within the basanite suite, one single olivine melilitite flow with high Mg# and abundant olivine and pyroxene megacrysts is the only primitive candidate for the nephelinite suite. However, in view of the large compositional gap and marked differences in incompatible element ratios, a relation between this flow and the nephelinites remains hypothetical. The variation within the evolved nephelinite series can be partly explained by fractionation of pyroxene, apatite, perovskite (and some nepheline), while magma mixing is indicated by zonation patterns of pyroxene. The most evolved nephelinite, however, differs significantly from all other nephelinites in major and trace elements. Thus the entire sequence is petrologically not a coherent evolution, rather the result of different mantle melts fractionating under variable conditions.Carved into the rift scarp of the study area west of Engare Sero is a young explosion crater, the Sekenge Crater. Sekenge Tuffs are olivine melilitites, similar to other craters and maars of the “Younger Extrusives” on the rift valley floor surrounding Oldoinyo Lengai. Further, still younger alkaline tuffs are found on the top of the rift shoulder. 相似文献
4.
T. F. D. Nielsen I. P. Solovova I. V. Veksler 《Contributions to Mineralogy and Petrology》1997,126(4):331-344
Perovskite and melilite crystals from melilitolites of the ultramafic alkaline Gardiner complex (East Greenland) contain
crystallised melt inclusions derived from: (1) melilitite; (2) low-alkali carbonatite; (3) natrocarbonatite. The melilitite
inclusion (1) homogenisation temperature of 1060 °C is similar to liquidus temperatures of experimentally investigated natural
melilitites. The compositions are peralkaline, low in MgO (ca.␣5 wt%), Ni and Cr, and they are low-pressure fractionates of
more magnesian larnite-normative ultramafic lamprophyre-type melts of primary mantle origin. Low-alkali carbonatite compositions
(2) homogenise at 1060–1030 °C and are compositionally similar to immiscible calcite carbonatite dykes derived from the melilitolite
magma. Natrocarbonatite inclusions (3) homogenise between 1030 and 900 °C and are compositionally similar to natrocarbonatite
lava from Oldoinyo Lengai. Nephelinitic to phonolitic dykes which are related to the calcite carbonatite dykes, are very Zr-rich
and agpaitic (molecular Na2O + K2O/Al2O3 > 1.2) and resemble nephelinites of Oldoinyo Lengai. The petrographic, geochemical and temporal relationships indicate unmixing
of carbonatite compositions (ca. 10% alkalies) from evolving melilitite melt and continued fractionation of melilitite to
nephelinite. It is suggested that the natrocarbonatite compositions represent degassed supercritical high temperature fluid
formed in a cooling body of strongly larnite-normative nephelinite or evolved melilitite. The Gardiner complex and similar
melilitolite and carbonatite-bearing ultramafic alkaline complexes are believed to represent subvolcanic complexes formed
beneath volcanoes comparable to Oldoinyo Lengai and that the suggested origin of natrocarbonatite may be applied to natrocarbonatites
of Oldoinyo Lengai.
Received: 18 January 1996 / Accepted: 2 September 1996 相似文献
5.
Natrocarbonatite flows in the crater of the volcano Oldoinyo Lengai (Tanzania) are the only carbonatite magmas observed to erupt and have provided strong arguments in favor of a magmatic origin for carbonatite. The currently favored explanation for the genesis of these carbonatites by liquid immiscibility between a silicate and a carbonatite melt is questioned based on the extremely low eruption temperatures of 544-593 °C and compositional and mineralogical characteristics not in agreement with experimental constraints. Experimental investigations of the relationship between Oldoinyo Lengai natrocarbonatite and related silicate rock compositions do indicate that alkali-bearing peralkaline carbonatite with liquidus calcite can form by liquid immiscibility. At the same time, these experiments result in evidence which speaks against a liquid immiscibility origin for the highly alkaline and peralkaline Oldoinyo Lengai natrocarbonatite. On the carbonatite side of the miscibility gap, fractional crystallization cannot account for a liquid evolution from alkali-bearing peralkaline carbonatite to highly alkaline natrocarbonatite. Such an evolution does not seem to be compatible with the liquidus mineral assemblages and the chemistry of Oldoinyo Lengai natrocarbonatite. No natural silicate magma is known to produce natrocarbonatite compositions by liquid immiscibility. The best interpretation of the Oldoinyo Lengai natrocarbonatite flows involves expulsion of a cognate, mobile, alkaline, and CO2-rich fluid condensate. This conclusion is supported by recent studies of silicate and carbonatite melt inclusions in minerals of ultramafic alkaline complexes, trace element partitioning, isotopic constraints, and by experimental data on major element partitioning between coexisting H2O-CO2-rich fluid and carbonatitic melt. In contrast to all other suggested modes of formation, an origin of Oldoinyo Lengai natrocarbonatite from cognate fluid appears best to be in agreement with the field observations, the petrography, mineralogy, and geochemistry of Oldoinyo Lengai natrocarbonatite and the dynamics of the Oldoinyo Lengai natrocarbonatite extrusion. 相似文献
6.
Tony D. Peterson 《Contributions to Mineralogy and Petrology》1989,102(3):336-346
Two fractionation trends in sodic alkaline ultramafic liquids have been predicted from experiments in subsystems of the join Di-Ak-Ne-Lc-Qz. The products of these trends are equated with contrasting suites of peralkaline nephelinites from two nephelinite-carbonatite volcanos of the south Gregory Rift, Shombole (southern Kenya) and Oldoinyo L'engai (northern Tanzania). In both trends, peralkalinity is interpreted to result from fractional crystallization of aluminous clinopyroxene. The Shombole trend has olivine nephelinite as its parental magma, and the differentiation products are mildly peralkaline [(Na+K)/Al1.15] nephelinites. It is the most common lineage observed in nephelinite-carbonatite centres. The Oldoinyo L'engai trend has melilitite or olivine-melilite nephelinite as its parental magma, and produces extremely peralkaline [(Na+K)/Al=1.4–2.3] wollastonite- and combeite- (Na2 Ca2Si3O9) bearing nephelinites. The presence of a reaction relation between wollastonite and liquid to produce combeite, indicated by corroded wollastonite phenocrysts armoured by combeite in some nephelinites from Oldoinyo L'engai, is confirmed by melting experiments. Combeite nephelinites from Oldoinyo L'engai were erupted simultaneously with natrocarbonatite ash, and are very similar in composition to silicate liquids that have been shown by experiment to be immiscible with natrocarbonatite. Because the L'engai trend is rarely expressed at extrusive centres (combeite has been recorded at only three localities), and combeite nephelinites are highly evolved magmas, it is unlikely that natrocarbonatite is primary to other carbonatite types. It is proposed that carbonatite liquid is exsolved at crustal pressures from a wide range of nephelinitic liquids: Mg-rich carbonatite from primitive, olivine-bearing alkaline ultramafic liquids, Ca-rich carbonatite from olivine-free nephelinites of low peralkalinity, and natrocarbonatite from strongly peralkaline combeite nephelinites. 相似文献
7.
Major and trace element and Sr, Nd and Pb isotope analyses are presented for thirteen olivine-melilitites from Namaqualand, South Africa. Major element variations are consistent with derivation from carbonated garnet-peridotite at depths of at least 100 km and trace element abundances indicate melt fractions of 4%. Ubiquitous negative K anomalies and low, buffered K2O concentrations are interpreted to reflect the effect of residual phlogopite during melting. It is suggested that phlogopite stability and low melt potassium saturation concentrations are enhanced by high CO2/(CO2 + H2O) conditions. Residual phlogopite can also account for low measured Rb/Sr, Ba/Sr and Th/U ratios in the melilitites. REE abundances are controlled by residual garnet and hence Sm/Nd ratios are low (0.13–0.18). U/Pb ratios vary from 0.05 to 5 and are a function of Pb concentration which is in turn controlled by residual Pb-rich phase (probably sulphide). Nd and Sr isotopes are comparable with OIB from St. Helena, although two samples extend to higher 87Sr/86Sr ratios. Present day Pb isotopes are much more variable and partly reflect radiogenic growth since emplacement as a result of the highly variable U/Pb ratios.
Many of the trace element characteristics of the melilitites are distinct from those of within-plate potassic magmas despite both being derived from phlogopite-bearing, enriched mantle source regions. This can be attributed to the depth at which source enrichment occurred and the subsequent control exerted by phlogopite and carbonate during melting. In contrast to melilitites, potassic magmas are derived from shallower depths under low CO2/(CO2 + H2O) conditions and at higher temperatures at which phlogopite melts more readily.
The incompatible element ratios of the melilitites are also similar to those both observed in HIMU ocean island basalts (OIB) and inferred for HIMU OIB source regions from isotope variations (viz, low Sm/Nd, Rb/Sr, K/Nb, Th/U and high U/Pb and Ce/Pb). It is suggested that HIMU OIB's may be derived from sources that have been subject to enrichment by a melt generated in the presence of residual phlogopite. 相似文献
8.
Oldoinyo Lengai, located in the Gregory Rift in Tanzania, is a world-famous volcano owing to its uniqueness in producing natrocarbonatite melts and because of its extremely high CO2 flux. The volcano is constructed of highly peralkaline [PI = molar (Na2O + K2O)/Al2O3 > 2–3] nephelinite and phonolites, both of which likely coexisted with carbonate melt and a CO2-rich fluid before eruption. Results of a detailed melt inclusion study of the Oldoinyo Lengai nephelinite provide insights into the important role of degassing of CO2-rich vapor in the formation of natrocarbonatite and highly peralkaline nephelinites. Nepheline phenocrysts trapped primary melt inclusions at 750–800 °C, representing an evolved state of the magmas beneath Oldoinyo Lengai. Raman spectroscopy, heating-quenching experiments, low current EDS and EPMA analyses of quenched melt inclusions suggest that at this temperature, a dominantly natritess-normative, F-rich (7–14 wt%) carbonate melt and an extremely peralkaline (PI = 3.2–7.9), iron-rich nephelinite melt coexisted following degassing of a CO2 + H2O-vapor. We furthermore hypothesize that the degassing led to re-equilibration between the melt and liquid phases that remained and involved 1/ mixing between the residual (after degassing) alkali carbonate liquid and an F-rich carbonate melt and 2/ enrichment of the coexisting nephelinite melt in alkalis. We suggest that in the geological past similar processes were responsible for generating highly peralkaline silicate melts in continental rift tectonic settings worldwide. 相似文献
9.
Roger H. Mitchell 《Contributions to Mineralogy and Petrology》2009,158(5):589-598
This study presents petrographic and compositional data for coexisting peralkaline silicate glass and quenched natrocarbonatite
melt in nepheline phenocrysts from the 24 September 2007 and July 2008 eruptions of the natrocarbonatite volcano Oldoinyo
Lengai (Tanzania). Data are also given for peralkaline residual glass in combeite nephelinite ash clasts occurring in the
March–April 2006 large volume natrocarbonatite flow. These data are considered to demonstrate the occurrence of liquid immiscibility
between strongly peralkaline Fe-rich nephelinite melt and natrocarbonatite at Oldoinyo Lengai. Compositional data for coexisting
silicate–carbonate pairs in conjunction with previous experimental studies suggest that the size of the field of liquid immiscibility
for carbonated nephelinitic magmas is a function of their peralkalinity. It is shown that peralkaline combeite wollastonite
nephelinite was present at Oldoinyo Lengai prior to, and during, the 24 September 2007 ash eruption. It is postulated that
the driving force for this major eruption was assimilation and decomposition of previously emplaced solid natrocarbonatite.
Assimilation resulted in the formation of the unusual hybrid nepheline–andradite–melilite–combeite–phosphate magma represented
by the 24 September 2007 ash. 相似文献
10.
Nd, Pb and Sr isotopic data from nephelinite lavas from the Tertiary nephelinite-carbonatite complex of Napak, eastern Uganda, show large isotopic variations that can only be attributed to open-system behaviour. Possible explanations of the data include mixing between nephelinitic melts derived from an isotopically heterogeneous mantle, or interaction between a HIMU melt and mafic granulites. In both models crystal fractionation, involving olivine and clinopyroxene, played an important role. Major element chemistry, textural evidence and isotopic data from clinopyroxene phenocrysts from the olivine-bearing nephelinites, suggest that the pyroxenes did not crystallize from their host liquids. The isotopic data from the clinopyroxene phenocrysts support an interpretation of crystal fractionation in an open magma system that was undergoing continuous isotopic change. This study emphasises the importance of using combined isotopic data from both whole rock and mineral phases to interpret the evolutionary history of a single eruptive centre. 相似文献
11.
《地学前缘(英文版)》2020,11(6):2157-2168
Mount Cameroon volcano has erupted several times in the 20th Century with documented eruptions in 1909, 1922, 1954, 1959, 1982, 1999 and 2000. Evidence of historic volcanism is represented by several older lava flows and lahar deposits around the flanks of the volcano. This study aims to assess the evolution of Mount Cameroon volcanism through its eruptive history via interpretation of mineralogical, whole rock geochemical and Pb, Sr, Nd isotope data generated from historic and recent lava flows. In this study, samples were collected from the 1959, 1982, 1999 and 2000 eruptions and from several historic eruption sites with unknown eruption dates.Evaluation of major and trace element data demonstrates that Mount Cameroon is geotectonically associated with within-plate Ocean Island Basalt Settings. More than 90% of the studied historic lavas (n = 29) classify as tephrites and basanites whereas the modern lavas (n = 38) are predominantly trachybasalts, demonstrating evolution from primitive to evolved lavas over time typically in response to fractional crystallization. Petrographically, the lavas are porphyritic with main mineral phases being olivine, clinopyroxene, plagioclase feldspars and Fe–Ti–Cr oxides. The 1982 lavas are predominantly aphyric and dominated by lath-shaped flow-aligned plagioclase in the groundmass. Olivine chemistry shows variable forsterite compositions from Fo60–89. Clinopyroxenes vary from diopside through augite to titanaugite with chemical composition ranges from Wo45En32Fs7 to Wo51En47Fs17. Plagioclase feldspars vary from labradorite (An56–70) to bytownite (An80–87). For the Fe–Ti–Cr oxides, calculated ulvöspinel component shows a wide variation from ulv38–87. CIPW-normative classification on the Di-Ol-Hy-Qz-Ne system shows that all Mount Cameroon lavas are nepheline-normative (Ne ranges from 4.20 wt.% to 11.45 wt.%).Radiogenic isotope data demonstrate that Mount Cameroon lavas are HIMU (or high μ = 238U/204Pb), characterized by 206Pb/204Pb = 20.19–20.46, 207Pb/204Pb = 15.63–15.69, 208Pb/204Pb = 40.01–40.30, 87Sr/86Sr = 0.70322–0.70339 (εSr = −21.37 to −18.96) and 143Nd/144Nd = 0.51276–0.51285 (εNd = +2.29 to +4.05). The historic lavas show stronger HIMU signature relative to the modern lavas, suggesting evolution towards less HIMU signatures over time. This study has revealed that Mount Cameroon volcanism has evolved from primitive magmas characterized by stronger HIMU signatures with high 206/204Pb and 208/204Pb isotopes, low SiO2 and high Mg, Ni, Cr content towards lower HIMU signatures with relatively higher SiO2, lower Mg, Cr and Ni compositions. The geochemical and isotopic changes, which account for the evolution of magmatism on Mount Cameroon occur over long periods of time because all the modern lavas erupted within the last 100 years are isotopically homogeneous, with very limited variation in SiO2 compositions. 相似文献
12.
Strongly silica-poor (ne-normative), mafic alkaline lavas generally represented by olivine nephelinites, nephelinites, melilitites, and olivine melilitites
have erupted at various locations during Earth's history. On the basis of bulk-rock Mg#, high concentrations of Na2O, TiO2, and K2O, and trace element geochemistry, it has been suggested that these lavas represent low-degree melts that have undergone little
crystal fractionationen route to the surface. Many of these lavas also carry high-pressure mantle material in the form of harzburgite, spinel lherzolite,
and variants of websterite xenoliths, and rare garnet-bearing xenoliths. However, phenocryst phases instead indicate that
these magmas cooled to variable extents during their passage. We note subtle, yet important, differences in terms of CaO,
Al2O3, CaO/AlP2O3, and CaO/MgO. High-pressure experimental melting studies in CMAS-CO2 (3-8 GPa) and natural lherzolitic systems (3GPa) demonstrate that at an isobar increasing F leads to a moderate decrease
in CaO + MgO, whereas CaO/MgO and CaO/Al2O3 sharply decrease. Relatively high CaO/Al2O3 indicates melting in the presence of garnet (>- 85 km). Studies also demonstrate that CO2-bearing lherzolitic systems, when compared with anhydrous ones, also have higher CaO content in the coexisting melt at a
given P and T. Comparison of the bulk-rock major-element chemistry of silica-poor, mafic alkaline lavas with experimentally
determined high-pressure melts indicates that melting of anhydrous mantle lherzolite or garnet pyroxenite is not able to explain
many of the major element systematics of the lavas. However, high-pressure partial melts of carbonated lherzolite have the
right major element trends. Among ocean islands, lavas from Samoa and Hawaii are perhaps the products of very low degree of
partial melting. Lavas from Gran Canaria and Polynesia represent products of more advanced partial melting. On continents,
lavas from South Africa and certain localities in Germany are the products of a very low degree of partial melting, and those
from Texas and certain other localities in Germany are products of a slightly more advanced degree of partial melting of a
carbonated lherzolite. Lavas from Deccan, Czech Republic, and Freemans Cove are the products of even more advanced degree
of partial melting. The mere presence of mantle xenoliths in some of these lavas does not necessarily mean that the erupted
lavas represent direct mantle melts. 相似文献
13.
Basanites and nephelinites from the Tertiary Rhön area (Germany), which are part of the Central European Volcanic Province (CEVP), have high MgO, Ni and Cr contents and prominent garnet signatures indicating that they represent near-primary magmas formed by melting of a CO2-bearing peridotitic mantle source at high pressure. The Pb and Hf isotope (and previously published Nd and Sr isotope) ratios of the Rhön lavas are rather uniform, whereas the Os isotope composition is highly variable. For the most primitive basanites, Pb, Os and Hf isotope compositions fall within the range of enriched MORB and some OIB. Other basanites and nephelinites with low Os concentrations have distinctly more radiogenic Os (187Os/188Os: 0.160–0.469) isotope compositions, which are inferred to originate from crustal contamination. The samples with the highest Os concentrations have the lowest Os isotope ratios (187Os/188Os(23 Ma): 0.132–0.135), and likely remain unaffected by crustal contamination. Together with their fairly depleted Sr, Nd and Hf isotope ratios, the isotopic composition of the Rhön lavas suggests derivation from an asthenospheric mantle source. Prominent negative K and Rb anomalies, however, argue for melting amphibole or phlogopite-bearing sources, which can only be stable in the cold lithosphere. We therefore propose that asthenospheric melts precipitated at the asthenosphere-lithosphere thermal boundary as veins in the lithospheric mantle and were remelted or incorporated after only short storage times (about 10–100 million years) by ascending asthenospheric melts. Due to the short residence time incorporation of the vein material imposes the prominent phlogopite/amphibole signature of the Rhön alkaline basalts but does not lead to a shift in the isotopic signatures. Melting of the lithospheric mantle cannot strictly be excluded, but has to be subordinate due to the lack of the respective isotope signatures, in good agreement with the fairly thin lithosphere observed in the Rhön area. The fairly radiogenic Pb isotope signatures are expected to originate from melting of enriched, low melting temperature portions incorporated in the depleted upper (asthenospheric) mantle and therefore do not require upwelling of deep-seated mantle sources for the Rhön or many other continental alkaline lavas with similar Pb isotope signatures. 相似文献
14.
The study of melt microinclusions in olivine megacrysts from meimechites and alkali picrites of the Maimecha–Kotui alkali ultramafic and carbonatite province (Polar Siberia) revealed that the melt compositions corrected for loss of olivine due to post-entrapment crystallization of olivine on inclusion walls (differentiates of primary meimechite magma) match well to the composition of nephelinites and olivine melilitites belonging to carbonatite magmatic series. Modeling of fractional crystallization of meimechite magmas results in the high-alkali melt compositions corresponding to the silicate–carbonate liquid immiscibility field. The appearance of volatile-rich melts at the base of magma-generating plume systems at early stages of partial melting can be explained by extraction of incompatible elements including volatiles, by near-solidus melts at low degrees of partial melting, and meimechites are an example of such magmas. Subsequent accumulation of CO2 in the residual melt results in generation of carbonate magma. 相似文献
15.
David W. Phelps David A. Gust Joseph L. Wooden 《Contributions to Mineralogy and Petrology》1983,84(2-3):182-190
Major and trace-element whole rock data, Nd and Sr isotopic data, and microprobe data have been collected from a suite of basanites, olivine nephelinites, and olivine melilite nephelinites from the Raton-Clayton volcanic field, New Mexico. Most of the lavas have geochemical characteristics that suggest they are primary upper mantle derived melts. The previously unreported occurrence of Type I and Type II ultramafic xenoliths in some of the lava flows supports this conclusion. All the lavas are strongly enriched in light REE, Sr, Ba, U, Th, and P2O5. 87Sr/86Sr ratios are 0.70394 to 0.70412 and 143Nd/144Nd ratios are equal to an epsilon value of +1.4; the data fall within the Nd-Sr correlation field. Trace-element modeling indicates that the lavas were last in equilibrium with a light-REE enriched mantle with a (La/Yb)N of two to nine. However, the Nd isotopic data indicate a source with a time integrated, chondritic normalized, Sm/Nd ratio of 1.01. To account for this discrepancy a metasomatic enrichment of the source is proposed. The timing of the enrichment event can only be constrained to less than 1 AE ago, and the isotopic composition of the premetasomatized source and the metasomatizing agent cannot be specified. However, geochemical constraints suggest a CO2-rich fluid enriched in incompatible elements as the likely metasomatizing agent 相似文献
16.
The minerals of Oldoinyo Lengai natrocarbonatite lavas are unstable under atmospheric conditions. Subsolidus mineral assemblages in natrocarbonatites were studied in 105 samples from contemporary eruptions ranging from present day to about 100 years old. The subsolidus minerals in natrocarbonatites were formed (i) along cracks on the lava surface from hot gases escaping during cooling, (ii) as atmospheric alteration by solution of water-soluble minerals, in particular halides and gregoryite, and by hydration of nyerereite under the influence of meteoric water and (iii) by reaction with fumarole gases. After solidification, the lavas were cut by a network of thin cracks, the edges of which are covered by polymineralic encrustations. Samples collected 2–24 h after eruption contain nahcolite, trona, sylvite, and halite with accessory kalicinite and villiaumite. Atmospheric humidity results immediately (≥ 2 h after eruption) in alteration of black lavas that is marked by the appearance of white powdery thermonatrite with nahcolite on the lava surface. Subsequent reaction (weeks, months, years) of natrocarbonatite with meteoric water and the atmosphere results in the formation of pirssonite, gaylussite, shortite, trona, thermonatrite, nahcolite and calcite. Generally, the first important step is the formation of pirssonite and the end-members are calcite carbonate rocks or loose aggregates. Fumarolic activity is common for the active northern crater of the volcano. Reaction of hot (54–141 °C) fumarolic gases with natrocarbonatite leads to the formation of sulphur, gypsum, calcite, anhydrite, monohydrocalcite, barite and celestine. Changes in mineralogy of the natrocarbonatite lead to substantial chemical transformation. The most obvious chemical changes in this process are the loss of Na, K, Cl and S, combined with an increase in H2O, Ca, Sr, Ba, F and Mn. The oxygen and carbon isotopic composition of altered natrocarbonatites shows a significant shift from the primary “Lengai Box” to high values of δ18O and δ13C. Calcite exhibits δ13C values between − 2‰ and − 4‰ PDB and δ18O values of + 23‰ to + 26‰ SMOW. The observed assemblages of secondary minerals formed by reaction with atmosphere and meteoric water, the changes in chemical composition of the natrocarbonatite and field observations suggest that alteration of natrocarbonatite is an open-system low-temperature process. It takes place at temperatures between 8 and 43 °C with the addition of H2O to the system and the removal of Na, K, Cl and S from the carbonatites. Low-temperature thermodynamic models developed for alkali carbonate systems can be used for the interpretation of Oldoinyo Lengai subsolidus mineralization. 相似文献
17.
Tony D. Peterson 《Contributions to Mineralogy and Petrology》1989,101(4):458-478
Shombole, a nephelinite-carbonatite volcano in south Kenya, erupted silicate lavas, carbonatite dikes and tuffs, and pyroclastic rocks similar to those at other East African alkaline centres. Shombole lavas containing cpx + nepheline + accessory minerals range from perovskite-bearing nephelinites (43% SiO2, volatile-free) to sphene-bearing and phonolitic nephelinites (46–49% SiO2) and phonolites (49–56% SiO2) and have low peralkalinity ([Na+K]/Al 1.15) which does not correlate with SiO2. Early fractionation of olivine and clinopyroxene strongly depleted Ni and Cr concentrations (10 ppm); fractionation of perovskite, melanite, sphene, and apatite produced negative correlations of all REE with SiO2. Many lavas contain cognate intrusive xenoliths and xenocrysts and oscillatory zoning is a common feature of clinopyroxene, nepheline, and melanite crystals, indicating recycling of intrusive material. Irregular calcite-rich bodies in many samples are interpreted as quenched immiscible Ca-carbonatite liquid, and [Ca-carbonate]-silicate liquid immiscibility is observed in experiments with one nephelinite. Chemical variation in the Shombole suite can be modeled as a combination of crystal fractionation (clinopyroxene and heavy minor phases) and retention of neutral density nepheline derived from disaggregated xenoliths entrained during emplacement of dike swarms. Six newly analyzed lavas from Oldoinyo L'engai, northern Tanzania, are geochemically similar to Shombole nephelinites except that they have relatively high Na2O+K2O (average 18% vs 12%) and Zr (average 680 ppm vs 400 ppm). They are extremely peralkaline and are not typical of nephelinites from other centres. Three with [Na+K]/Al1.5 contain euhedral wollastonite phenocrysts; three with [Na+K]/Al2.0 contain combeite (Na2Ca2Si3O9) phenocrysts and pseudomorphs after wollastonite. Both types contain abundant sodalite phenocrysts (+nepheline+clinopyroxene+melanite+sphene). Seven other wollastonite nephelinite samples from L'engai have been described, but it is a lava type rarely seen in other centres. Combeite has been described from only two other locations (Mt. Shaheru, Zaire; Mayener Feld, Eifel). The hyperalkaline L'engai nephelinites have compositions similar to those of experimental silicate liquids immiscible with natrocarbonatite. Textural evidence for both carbonate-silicate (as carbonate globules) and silicate-silicate (as two optically discrete glasses with distinct compositions) liquid immiscibility is observed in the samples. 相似文献
18.
Geochemistry of an oceanite-ankaramite-basalt suite from East Island,Crozet Archipelago 总被引：1，自引：0，他引：1
Bernard M. Gunn Ramon Coy-Yll Norman D. Watkins Christian E. Abranson Jacques Nougier 《Contributions to Mineralogy and Petrology》1970,28(4):319-339
The petrology and geochemistry of East Island have been investigated for the first time. The island is a deeply dissected remnant of a Pleistocene shield volcano, one of several emerging from an oceanic rise forming part of the southwest branch of the Indian Ocean ridge system. The lavas form a flat-lying sequence of oceanites, ankaramites, olivine basalts and feldsparphyric basalts, the ankaramites containing 1 cm phenocrysts of diopsidic clinopyroxene. X-Ray fluorescence analyses were made of 43 lavas for the major elements plus Cr, Ni, Rb, Sr, Ba, Pb, and Th and the minerals were analysed by electron microprobe. The elements Mg, Cr, and Ni are strongly concentrated in spinel, olivine and clinopyroxene phases and in the ankaramites and oceanite lavas with maximum concentrations of 18% MgO, 1,000 ppm Cr, 380 ppm Ni, while Al, Ti, K, Rb, Ba, Th, Na, P, Sr concentrate in the groundmass and in the feldspathic and aphyric basalts. The elements Si, Ca, Fe and Mn remain virtually constant throughout the series.Correlations of +0.95 or better exist between the concentrations of elements within the two groups given above, and negative correlations between elements in different groups. The fractionation trends are unique with respect to the constant Al/Ti ratio and K/Sr ratio, but all trends may be reproduced by calculating the effect of subtraction of suitable amounts of chromite, olivine and low Ti clinopyroxene from an alkaline olivine basalt parent. Either fractionation has taken place involving these three phases under low pressure conditions or it is the result of different degrees of partial melting of mantle material.A complex magnesian chrome spinel is found in the ankaramites and is often jacketed by a chromian titanomagnetite. A complete series of intermediate compositions appears to exist between the two end members. 相似文献
19.
Trace Element Geochemistry of Tertiary Continental Alkali Basalts from the Liuhe—Yizheng Area,Jiangsu Province,China 总被引：5，自引：0，他引：5
支霞臣 《中国地球化学学报》1991,10(3):204-216
Reported in this paper are the chemical compositions and trace element (REE,Ba,Rb,Sr,Nb,Zr,Ni,Cr,V,Ga,Y,Sc,Zn,Cu,etc)abundances of Tertiary continental alkali basalts from the Liube-yizheng area,Jiangsu Province,China.The olivine basalt,alkali olivine basalt and basanite are all derived from evolved melts which were once af-fected by different degrees of fractional crystallization of olivine and clinopyroxene(1:2)under high pres-sures.The initial melts were derived from the garnet lherzolite-type mantle source through low-degree par-tial melting.The mantle source has been affected by recent mantle-enrichment events(e.g.mantle metasomatism),resulting in incompatible trace element enrichment and long-term depletion of radiogenic isotopic compositions of Sr and Nd. 相似文献
20.
Petrogenesis of isotopically unusual Pliocene olivine leucitites from Deep Springs Valley, California 总被引：2，自引：0，他引：2
High-K mafic alkalic lavas (5.4 to 3.2 wt% K2O) from Deep Springs Valley, California define good correlations of increasing incompatible element (e.g., Sr, Zr, Ba, LREE)
and compatible element contents (e.g., Ni, Cr) with increasing MgO. Strontium and Nd isotope compositions are also correlated
with MgO; 87Sr/86Sr ratios decrease and ɛNd values increase with decreasing MgO. The Sr and Nd isotope compositions of these lavas are extreme compared to most other
continental and oceanic rocks; 87Sr/86Sr ratios range from 0.7121 to 0.7105 and ɛNd values range from −16.9 to −15.4. Lead isotope ratios are relatively constant, 206Pb/204Pb ∼17.2, 207Pb/204Pb ∼15.5, and 208Pb/204Pb ∼38.6. Depleted mantle model ages calculated using Sr and Nd isotopes imply that the reservoir these lavas were derived
from has been distinct from the depleted mantle reservoir since the early Proterozoic. The Sr-Nd-Pb isotope variations of
the Deep Springs Valley lavas are unique because they do not plot along either the EM I or EM II arrays. For example, most
basalts that have low ɛNd values and unradiogenic 206Pb/204Pb ratios have relatively low 87Sr/86Sr ratios (the EM I array), whereas basalts with low ɛNd values and high 87Sr/86Sr ratios have radiogenic 206Pb/204Pb ratios (the EM II array). High-K lavas from Deep Springs Valley have EM II-like Sr and Nd isotope compositions, but EM
I-like Pb isotope compositions. A simple method for producing the range of isotopic and major- and trace-element variations
in the Deep Springs Valley lavas is by two-component mixing between this unusual K-rich mantle source and a more typical depleted
mantle basalt. We favor passage of MORB-like magmas that partially fused and were contaminated by potassic magmas derived
from melting high-K mantle veins that were stored in the lithospheric mantle. The origin of the anomalously high 87Sr/86Sr and 208Pb/204Pb ratios and low ɛNd values and 206Pb/204Pb ratios requires addition of an old component with high Rb/Sr and Th/Pb ratios but low Sm/Nd and U/Pb ratios into the mantle
source region from which these basalts were derived. This old component may be sediments that were introduced into the mantle,
either during Proterozoic subduction, or by foundering of Proterozoic age crust into the mantle at some time prior to eruption
of the lavas.
Received: 28 February 1997 / Accepted: 9 July 1998 相似文献