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1.
The Kahoolawe shield volcano produced precaldera and caldera-filling tholeiites and mildly alkalic post-caldera lavas that petrographically and compositionally resemble such lavas from other Hawaiian shield volcanoes. However, Kahoolawe tholeiites display wide ranges in incompatible trace element ratios (e.g., Nb/Th=9–24, Th/Ta=0.6–1.3), 87Sr/86Sr (0.70379–0.70440), 143Nd/144Nd (0.51273–0.51298), and 206Pb/204Pb (17.92–18.37). The isotopic variation exceeds that at any other Hawaiian shield volcano, and spans about half the range for all Hawaiian tholeiites. Quasi-cyclic temporal evolution of Kahoolawe tholeiites is consistent with combined fractional crystallization and periodic recharge by primitive magmas. Ratios of highly incompatible trace elements and Sr, Nd, and Pb isotopic ratios from coherent sub-trends that reflect recurrent interactions between variably evolved magmas and two other mantle components whose compositions are constrained by intersections between these trends. The most MgO-rich Kahoolawe tholeiites are partial melts of a high Nb/Th (23.5) ascending plume, possibly comprising ancient subducted oceanic lithosphere. Slightly evolved tholeiites experienced combined crystal fractionation and assimilation (AFC) of material derived from a distinct reservoir (Nb/Th 9) of asthenospheric derivation. The most evolved tholeiites display compositional shifts toward a third component, having mid ocean ridge basalt-like isotopic ratios but enriched OIB-like trace element ratios, representing part of the lithospheric mantle (or melts thereof). Periodic recurrence of all three magma variants suggests that eruptions may have tapped coeval reservoirs distributed over a large depth range. Kahoolawe provides new evidence concerning the nature of the Hawaiian plume, the distribution of compositional heterogeneities in the suboeanic mantle, and the processes by which Hawaiian tholeiites form and evolve.  相似文献   

2.
Jurassic age volcanic rocks of the Stonyford volcanic complex(SFVC) comprise three distinct petrological groups based ontheir whole-rock geochemistry: (1) oceanic tholeiites; (2) transitionalalkali basalts and glasses; (3) high-Al, low-Ti tholeiites.Major and trace element, and Sr–Nd–Pb isotopic dataindicate that the oceanic tholeiites formed as low-degree partialmelts of normal mid-ocean ridge basalt (N-MORB)-source asthenospheresimilar in isotope composition to the East Pacific Rise today;the alkalic lavas were derived from an enriched source similarto that of E-MORB. The high-Al, low-Ti lavas resemble second-stagemelts of a depleted MORB-source asthenosphere that formed bymelting spinel lherzolite at low pressures. Trace element systematicsof the high-Al, low-Ti basalts show the influence of an enrichedcomponent, which overprints generally depleted trace elementcharacteristics. Tectonic discrimination diagrams show thatthe oceanic tholeiite and alkali suites are similar to present-daybasalts generated at mid-oceanic ridges. The high-Al, low-Tisuite resembles primitive arc basalts with an enriched, alkalibasalt-like overprint. Isotopic data show the influence of recycledcomponents in all three suites. The SFVC was constructed ona substrate of normal Coast Range ophiolite in an extensionalforearc setting. The close juxtaposition of the MORB-like olivinetholeiites with alkali and high-Al, low-Ti basalts suggestsderivation from a hybrid mantle source region that includedMORB-source asthenosphere, enriched oceanic asthenosphere, andthe depleted supra-subduction zone mantle wedge. We proposethat the SFVC formed in response to collision of a mid-oceanridge spreading center with the Coast Range ophiolite subductionzone. Formation of a slab window beneath the forearc duringcollision allowed the influx of ridge-derived magmas or themantle source of these magmas. Continued melting of the previouslydepleted mantle wedge above the now defunct subduction zoneproduced strongly depleted high-Al, low-Ti basalts that werepartially fertilized with enriched, alkali basalt-type meltsand slab-derived fluids. KEY WORDS: CRO; oceanic basalts; California  相似文献   

3.
Geochemistry of tholeiites from Lanai,Hawaii   总被引：3，自引：0，他引：3  
Lanai is the third smallest of the fifteen principal subaerial shield volcanoes of the Hawaiian hotspot. This volcano apparently became extinct during the shield-building stage of volcanism, as shown by the absence of both alkalic cap and post-erosional lavas. Major and trace element analyses of 22 new samples collected primarily from 3 stratigraphic sections show that Lanai tholeiites span a large range in composition. Some Lanai lavas are unique geochemically among Hawaiian tholeiites in having the lowest abundances of incompatible trace elements of any Hawaiian lavas and well-developed positive Eu anomalies. The geochemical characteristics of these low-abundance Lanai tholeiites are not the result of alteration, differences in mantle source modal mineralogy, the presence of residual accessory mantle phases or fractional crystallization of such phases, assimilation of depleted [MORB] wall-rock, or accumulation/resorption of phenocrysts or xenocrysts. Incompatible trace element ratios (e.g., Nb/La, Nb/Th, La/Th, La/Hf, Ce/Pb) in Lanai tholeiites span considerable ranges and form coherent trends with each other and with absolute abundances of these elements. Large variations in La/Sm, La/Yb, and absolute REE abundances at constant MgO suggest that Lanai tholeiites formed by variable amounts of partial melting. However, large ranges in incompatible element ratios cannot be explained solely by variations in partial melting of a geochemically homogeneous source, but must reflect geochemical heterogeneities in the Lanai source. Partial melting modeling indicates that the mixed Lanai source is probably LREE-enriched [i.e., (La/Yb)CN>1]. One component in the Lanai source, exemplified by the low-abundance tholeiites, has markedly lower REE/HFSE, Th/HFSE, alkali/HFSE, and Ce/Pb ratios than other Lanai or Hawaiian tholeiites and may indicate the presence of recycled residual subduction zone materials in the Hawaiian plume source. The positive Eu anomalies that characterize the low-abundance Lanai tholeiites are not the result of plagioclase accumulation or assimilation but are a feature of this source component. Progressive temporal geochemical variations in Lanai tholeiites from 2 stratigraphic sections indicate that the source composition of these lavas probably evolved over time. This change could have resulted from a progressive decrease in the extent of partial melting of the Lanai source. The compositional variability of Lanai tholeiites suggests that geochemical heterogeneities in their source are larger than the scale of partial melting. Lanai tholeiites could not have formed by smaller degrees of partial melting of plume material than did the larger-volume Hawaiian shields. Therefore, volume differences between Hawaiian shields must be controlled primarily by differences in the volume of supplied plume material rather than by differences in the degree of partial melting. The premature cessation of eruptive activity at Lanai may be attributed to relatively large degrees of partial melting of a small plume.  相似文献   

4.
Twenty-three basalts from northwestern Formosa were analyzed for Si, Ti, Al, Fe, Mg, Ca, Na, K, Rb, Sr, Hf, Co, Sc, Cr, Th, and 7 REE. Formosan alkalic basalts are generally similar to most alkalic basalts, and Formosan tholeiites are somewhat similar to island arc and continental tholeiites in terms of trends in K/Rb, Rb/Sr, K/Sr, and Ca/Sr ratios. Compared to most submarine tholeiites, Formosan tholeiites are enriched in Rb relative to K and Sr, and enriched in Sr relative to K and Ca. Both types of Formosan basalts show, relative to chondritic proportions, enrichments in light REE which smoothly decrease through the heavy REE. Their REE patterns are similar to those observed in Dogo-Oki alkalic basalts, Hawaiian basalts, and Deccan Plateau basalt, but differ strikingly from those of Japanese tholeiites and oceanic ridge basalts. These relationships and contrasts suggest that Formosan basalts originated in a plagioclase-free portion of the upper mantle and at greater depths that did Japanese tholeiites and oceanic ridge basalts.  相似文献   

5.
The Miocene to Quaternary lavas of northwestern Syria range from basanite, alkali basalts, and tholeiites to basaltic andesites, hawaiites, and mugearites. Crustal assimilation and fractional crystallization processes (AFC) modified the composition of the mantle derived magmas. Crustal assimilation is indicated by decreasing Nb/U (52.8–17.9) and increasing Pb/Nd (0.09–0.21) and by variable isotopic compositions of the lavas (87Sr/86Sr: 0.7036–0.7048, 143Nd/144Nd: 0.51294–0.51269, 206Pb/204Pb: 18.98–18.60) throughout the differentiation. Modeling of the AFC processes indicates that the magmas have assimilated up to 25% of continental upper crust. The stratigraphy of the lavas reveals decreasing degrees and increasing depths of melting with time and the strongly fractionated heavy rare earth elements indicate melt generation in the garnet stability field. Modeling of melt formation based on trace element contents suggests that 8–10% melting of the asthenospheric mantle source produced the tholeiites, whereas basanite and alkali basalts are formed by 2–4% melting of a similar source.Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.  相似文献   

6.
韩江伟  熊小林  朱照宇 《岩石学报》2009,25(12):3208-3220
对雷琼地区21个晚新生代玄武岩样品的主量、微量元素和Sr、Nd、Pb同位素分别用湿化学法、ICP-MS和MC-ICPMS进行了测定.这些玄武岩主要为石英拉斑玄武岩,其次为橄榄拉斑玄武岩和碱性玄武岩.大多数样品的微量元素和同位素成分与洋岛玄武岩(OIBs)相似,而且随着SiO_2不饱和度增加,不相容元素含量也增加.除R4-1可能受到地壳混染外,其他样品相对均一的Nd同位素(ε_(Nd)=2.5-6.0)以及变化明显但范围有限的Sr同位素(0.703106～0.704481),可能继承了地幔源区的特征.~(87)Sr/~(86)Sr与~(206)Pb/~(204)Pb的正相关和~(143)Nd/~(144)Nd与~(206)Pb/~(204)Pb的负相关特征暗示DM(软流圈地幔)与EM2(岩石圈地幔)的混合.地幔捕虏体的同位素特征暗示EM2成分不可能存在于尖晶石橄榄岩地幔,而La/Yb和Sm/Yb系统表明岩浆由石榴石橄榄岩部分熔融产生,这意味着EM2成分可能存在于石榴石橄榄岩地幔.雷琼地区玄武岩的地球化学变化可以用软流圈地幔为主的熔体加入不同比例石榴石橄榄岩地幔不同程度熔融产生的熔体来解释:碱性玄武岩和橄榄拉斑玄武岩是软流圈熔体与石榴石橄榄岩地幔较低程度(7%～9%)熔融体混合,而石英拉斑玄武岩是软流圈熔体与石榴石橄榄岩地幔较高程度(10%～20%)熔融体的混合.  相似文献   

7.
《Geochimica et cosmochimica acta》1999,63(23-24):4119-4138
Measurements of 238U-230Th-226Ra and 235U-231Pa disequilibria in a suite of tholeiitic-to-basanitic lavas provide estimates of porosity, solid mantle upwelling rate and melt transport times beneath Hawaii. The observation that (230Th/238U) > 1 indicates that garnet is required as a residual phase in the magma sources for all of the lavas. Both chromatographic porous flow and dynamic melting of a garnet peridotite source can adequately explain the combined U-Th-Ra and U-Pa data for these Hawaiian basalts. For chromatographic porous flow, the calculated maximum porosity in the melting zone ranges from 0.3–3% for tholeiites and 0.1–1% for alkali basalts and basanites, and solid mantle upwelling rates range from 40 to 100 cm yr−1 for tholeiites and from 1 to 3 cm yr−1 for basanites. For dynamic melting, the escape or threshold porosity is 0.5–2% for tholeiites and 0.1–0.8% for alkali basalts and basanites, and solid mantle upwelling rates range from 10 to 30 cm yr−1 for tholeiites and from 0.1 to 1 cm yr−1 for basanites. Assuming a constant melt productivity, calculated total melt fractions range from 15% for the tholeiitic basalts to 3% for alkali basalts and basanites.  相似文献   

8.
A total of 17 alkali basalts (alkali olivine basalt, limburgite, olivine nephelinite) and quartz tholeiites, and of 10 peridotite xenoliths (or their clinopyroxenes) were analyzed for Nd and Sr isotopes. 143Nd/144Nd ratios and 87Sr/86Sr ratios of all basalts and of the majority of ultramafic xenoliths plot below the mantle array with a large variation in Nd isotopes and a smaller variation in Sr isotopes. The tholeiites were less radiogenic in Nd than the alkali basalts. Volcanics from the Eifel and Massif Central regions contain Nd and Sr, which is more radiogenic than that of the basalts from the Hessian Depression. Nd and Sr isotopic compositions of all rocks from the latter area, with the exception of one tholeiite and one peridotite plot in the same field of isotope ratios as the Ronda ultramafic tectonite (SW Spain), which ranges in composition from garnet to plagioclase peridotite. The alkali basaltic rocks are products of smaller degrees of partial melting of depleted peridotite, which has undergone a larger metasomatic alteration compared with the source rock of tholeiitic magmas. For the peridotite xenoliths such metasomatic alteration is indicated by the correlation of their K contents and isotopic compositions. We assume that the upper mantle locally can acquire isotopic signatures low in radiogenic Nd and Sr from the introduction of delaminated crust. Such granulites low in radiogenic Nd and Sr are products of early REE fractionation and granite (Rb) separation.  相似文献   

9.
The postshield and posterosional stages of Haleakala Volcano contain intercalated alkalic basalt and evolved alkalic lavas. Isotopic and incompatible element abundance ratios in the Haleakala postshield basalts changed systematically with time, providing evidence for significant temporal changes in the mantle components contributing to the magmatic sources. Specifically, a depleted, i.e. low87Sr/86Sr and high143Nd/144Nd, mantle component is more abundant in younger lavas. However, as magma-production rates decreased during the postshield and posterosional stages, basaltic melts in magma reservoirs cooled and fractionated, leading to evolved residual melts such as hawaiite. Because primary basalt compositions changed with time, the evolved Haleakala lavas formed from a range of parental compositions. However, basalts and evolved lavas of similar age and isotopic ratios (Sr and Nd) have major and trace element contents that are consistent with a crystal-fractionation model. Although alkalic basalt and hawaiite are the dominant lavas of the postshield stages of both Haleakala and Mauna Kea volcanoes, there are important differences between their lavas. For example, compositional differences between the hawaiite suites at Haleakala and Mauna Kea indicate that, on average, the evolved lavas at Haleakala formed at lower pressures. Also, at Haleakala basalts are intercalated with hawaiites, whereas at Mauna Kea basalts and hawaiites are separated by a sharp boundary. These differences probably reflect a higher magma supply rate to the Haleakala volcano.  相似文献   

10.
The simplified model of basalt genesis described in Part I of this series, equilibrium partial melting followed by Rayleigh-type fractional crystallization, is applied to a stratigraphically controlled sequence of basalt flows from Kohala volcano. Major-element compositions were determined for 52 samples and show a time-stratigraphic progression from tholeiites through transitional basalts to alkali basalts. Twenty-six of these samples were analyzed by isotope dilution for K, Rb, Cs, Sr, Ba and the REE, 13 for87Sr/86Sr, and 19 for Co, Cr, Ni and V by atomic absorption. After a simple, first-order correction for the effects of fractional crystallization (involving mostly olivine and aluminous clinopyroxene), the major element concentrations cluster tightly, and the incompatible trace elements show monotonic increases in concentration as a function of stratigraphic height. The process identification plot shows that all the (fractionation corrected) melt compositions can be explained by equilibrium partial melting of compositionally identical batches of source material. The REE and Sr are fractionated because of the presence of residual clinopyroxene. Garnet may also be present but in much smaller amounts. In this respect our results differ significantly from those of Leeman et al. (1980). The calculated chondrite-normalized REE patterns of the source are nearly flat to slightly convex upward. Therefore there is no need to invoke special mechanisms, such as metasomatic REE preenrichment of the source, in order to explain the petrogenesis of the suite of lavas. Specifically, Ce concentrations ranging from 20 to 250 times chondritic are all explained by the same calculated source pattern having a chondrite-normalized ratio of Ce/Sm=0.9±0.2. However, the normalized ratio Ce/Ba?2 shows that the source is not simply primitive mantle.  相似文献   

11.
A wide compositional continuum of basalts has been erupted from near-ridge seamounts constructed on the Cocos Plate between the Clipperton and Orozco Francture Zones. They range from highly evolved to moderately primitive (3.0–7.8% MgO), LREE-enriched alkali basalts, to moderately evolved to near-primary (5.2–9.5% MgO) tholeiites indistinguishable from N-type MORB. The data set of 159 quench glass analyses exhibits a remarkably consistent variation in both major and trace element composition that is keyed to variations in (La/Sm). Modeling of potential liquid lines of descent at pressures ranging from 1 bar to 8 kbar shows that this covariation is partially due to systematic differences in liquid lines of descent, where the alkaline lavas have undergone substantially more high pressure clinopyroxene fractionation and substantially less low pressure plagioclase fractionation than the tholeiites. In addition, systematic variation in the composition of the more primitive glasses indicates that they were derived from mixing of discrete enriched and depleted melts in the heterogenous seamount mantle source at pressures of 8–10 kbar and greater, and that clinopyroxene may be a residual phase during partial melting. These results show that porous media flow in the seamount mantle source is minor and that melt transport is accomplished primarily through cracking and diking. This study supports suggestions that the general homogeneity of basalt along the EPR is due to mixing in sub-axial magma chambers and mush zones, with additional mixing during partial mantle melting and melt segregation.  相似文献   

12.
A convergent margin magma series with characteristic low Nband Ta abundances and enrichments in alkalis and alkaline earthsis intercalated with typical intraplate alkalic basalts in aback-arc setting, 200–250 km above the Wadati-Benioffzone on the North Island, New Zealand. These two contrastingmagma types, together with late-stage K-rich maflc lavas, wereerupted over a short time period (1{dot}60–2{dot}74 Ma)and constitute the Alexandra Volcanics. Field relationshipsindicate that these diverse magma types were contemporaneous,and thus their mantle source regions coexisted, in a singletectonic environment. The convergent margin magma series forms a linear chain of stratovolcanoesaligned at right angles to the present subduction zone. Closed-systempolybaric fractional crystallization models can explain theevolution from ankaramites to transitional olivine basalts toolivine tholeiites to high-Al basalts to medium- and high-Kandesites. The most primitive lavas have geochemical (high LIL/LREEand LIL/HFS element ratios) and Sr, Nd, and Pb isotopic compositionstypical of convergent margin magmas. Calculated source compositionssuggest that three components are involved: a MORB component,a component derived from subducted oceanic crust, and a contributionfrom subducted sediments. The alkalic basalts occur as dispersed monogenetic volcanoesand are intercalated with the larger convergent margin stratovolcanocs.These basalts are enriched in LILE, LREE, Nb, and Ta, and havelow Ba/Nb and Ba/La ratios, all of which are characteristicof ocean island (intraplate) basalts (OIBs). Their relativelyhigh Nd (+5{dot}5 and low 87Sr/86Sr(0{dot}703l–0{dot}7036)are also typical of OIBs. These alkalic magmas were derivedfrom the underlying continental lithospheric mantle that hasbeen enriched by upward-migrating silica-undersaturated melts,probably including volatiles, from the low- velocity zone. Asubducted slab component is not required to account for theirincompatible element enriched character. The K-rich mafic lavas, basanites, and absarokites are volumetricallyminor and cap the largest of the stratovolcanoes, Pirongia.The basanites have geochemical and isotopic compositions whichsuggest they are mixtures of multiple source components, includingthe alkalic and convergent margin region.  相似文献   

13.
Rare Earth Element Inversions and Percolation Models for Hawaii   总被引：2，自引：4，他引：2  
WATSON  SARAH 《Journal of Petrology》1993,34(4):763-783
A detailed study has been made of the evolution with time ofthe mantle source and degree of melting required to producea typical Hawaiian volcano. The preshield stage involves a changefrom a depleted to a primitive mantle source and an increasein the melt fraction. Important intra- and inter-volcano variationsoccur during the shield stage which may be related to melt transportprocesses. With time, Mauna Loa's lavas show depletion in increasinglycompatible elements, a result which is consistent with percolationprocesses. Postshield magmas are generated by very small degreesof melting of a depleted mantle source and may be importantin the development of posterosional volcanism. Posterosionallavas can be generated by variable degrees of melting of anamphibole-bearing source that has been enriched by postshieldmagma. A simple percolation model is consistent with the isotopic evolutionof Hawaiian volcanoes. All of the observed isotopic variationseen between Hawaiian volcanoes may be produced from only twomantle sources by small variations in the percolation processes. * Present address: Department of Earth Sciences, Parks Road, Oxford OX1 3PR, UK.  相似文献   

14.
Previous studies of alkalic lavas erupted during the waning growth stages (<0.9 Ma to present) of Haleakala volcano identified systematic temporal changes in isotopic and incompatible element abundance ratios. These geochemical trends reflect a mantle mixing process with a systematic change in the proportions of mixing components. We studied lavas from a 250-m-thick stratigraphic sequence in Honomanu Gulch that includes the oldest (1.1 Ma) subaerial basalts exposed at Haleakaka. The lower 200 m of section is intercalated tholeiitic and alkalic basalt with similar isotopic (Sr, Nd, Pb) and incompatible element abundance ratios (e.g., Nb/La, La/Ce, La/Sr, Hf/Sm, Ti/Eu). These lava compositions are consistent with derivation of alkalic and tholeiitic basalt by partial melting of a compositionally homogeneous, clinopyroxene-rich, garnet lherzolite source. The intercalated tholeiitic and alkalic Honomanu lavas may reflect a process which tapped melts generated in different portions of a rising plume, and we infer that the tholeiitic lavas reflect a melting range of 10% to 15%, while the intercalated alkalic lavas reflect a range of 6.5% to 8% melting. However, within the uppermost 50 m of section. 87Sr/86Sr decreases from 0.70371 to 0.70328 as eruption age decreased from 0.97 Ma to 0.78 Ma. We infer that as lava compositions changed from intercalated tholeiitic and alkalic lavas to only alkalic lavas at 0.93 Ma, the mixing proportions of source components changed with a MORB-related mantle component becoming increasingly important as eruption age decreased.  相似文献   

15.
The Sete Cidades volcano (São Miguel, Azores) is situatedat the eastern end of the ultraslow spreading Terceira riftaxis. The volcano comprises several dominantly basaltic pre-calderaeruptions, a trachytic caldera-forming stage and a post-calderastage consisting of alternating trachytic and basaltic eruptions.The post-caldera flank lavas are more primitive (>5 wt %MgO) than the pre-caldera lavas, implying extended fractionalcrystallization and longer crustal residence times for the pre-caldera,shield-building lavas. Thermobarometric estimates show thatthe ascending alkali basaltic magmas stagnated and crystallizedat the crust–mantle boundary (15 km depth), whereas themore evolved magmas mainly fractionated in the upper crust (3km depth). The caldera-forming eruption was triggered by a basalticinjection into a shallow trachytic magma chamber. Lavas fromall stages follow a single, continuous liquid line of descentfrom alkali basalt to trachyte, although slight differencesin incompatible element (e.g. Ba/Nb, La/Nb) and Sr isotope ratiosimply some heterogeneity of the mantle source. Major and traceelement data suggest similar partial melting processes throughoutthe evolution of the volcano. Slight geochemical differencesbetween post- and pre-caldera stage lavas from the Sete Cidadesvolcanic system indicate a variation in the mantle source compositionwith time. The oxygen fugacity increased from the pre-calderato the post-caldera stage lavas, probably as a result of theassimilation of crustal rocks; this is supported by the presenceof crustal xenoliths in the lavas of the flank vents. The lavasfrom the Sete Cidades volcano generally have low Sr isotoperatios; however, rocks from one post-caldera vent on the westernflank indicate mixing with magmas resembling the lavas fromthe neighbouring Agua de Pau volcano, having higher Sr isotoperatios. The different magma sources at Sete Cidades and theadjacent Agua de Pau volcano imply that, despite their closeproximity, there is only limited interaction between them. KEY WORDS: crystallization depth; fractionation; stratigraphy; Terceira rift; volcanic stages  相似文献   

16.
Cenozoic lavas from Hainan Island,South China,comprise quartz tholeiite,olivine tholeiite,alkali basalt,and basanite and form a continuous,tholeiite-dominated,compositional spectrum.Highly incompatible elements and their relationships with isotopes in these lavas are shown to be useful in evaluating mantle-source composition,whereas modeling suggests that ratios of elements with bulk partition coefficients significantly larger than those of Nb and Ta may be sensitive to partial melting.Th/Ta and La/Nb ratios of alkali basalts are lower than those of tholeiites,and they are all lower than those of the primitive mantle,These ratios correlate positively with ^207Pb/^204Pb and ^87Sr/^86Sr ratios.Such relationships can be explained by mixing of depleted and enriched source components.A depleted component is indicated by alkali basalt compositions and is similar to some depleted OIB (PREMA).The enriched component,similar to sediment compositions,is indicated by tholeiites with high LILE/HFSE,^207Pb/^204Pb,and ^87Sr/^86Sr ratios.In general,basalts from Hainan and the South China Basin(SCB)share common geochemical characters.e.g.high Rb/Sr,Th/Ta,^207Pb/^206Pb,and low Ba/Th ratios.Such a geochemical trend is comparable to that of EMII-type OIB and best explained as the result of subduction.Occurrence of these characteristics in both continental Hainan basalts and SCB seamout basalts indicates the presence of a South China geochemical domain that exists in the mantle region below the lithosphere.  相似文献   

17.
The petrology and geochemistry of the Azores Islands   总被引：7，自引：0，他引：7  
Forty lavas from the Azores Islands have been analyzed for 87Sr/86Sr ratios, major elements, first transition series metals, and LIL elements. The samples belong to the alkali basalt magma series but range from transitional hy-normative basalts from Terceira to basanitoids from Santa Maria. Differentiated lavas include both typical trachytes and comenditic trachytes and comendites. Major and trace element concentrations define smooth trends on variation diagrams, and these trends can be related to phases crystallizing in the rocks. Systematic interisland differences are also apparent in these variation diagrams. LIL element concentrations in island basalts are roughly twice as high as those in tholeiites from the adjacent Mid-Atlantic Ridge which transects the Azores Plateau. 87Sr/86Sr ratios in lavas from 6 of the 9 islands range from 0.70332 to 0.70354, a range similar to that found in tholeiites from the Mid-Atlantic Ridge transect of the Azores Plateau. This suggests that lavas from these islands and this portion of the Mid-Atlantic Ridge may be derived from a similar source. However, lavas from the islands of Faial and Pico have 87Sr/86Sr ratios up to 0.70394 and ratios in Sao Miguel lavas range up to 0.70525, suggesting basalts from these islands are derived from a chemically distinct source. Differences in the average LIL element concentrations of the least fractionated ridge tholeiites from the Azores Plateau and alkali basalts from the islands result from differences in extent of partial melting and residual mineralogy. The alkali basalts are derived by roughly half as much melting as are the tholeiites. Trace element concentrations in Azores peralkaline lavas preclude their derivation by partial melting of peridotitic mantle or basaltic crust; rather the data suggest they are produced by fractional crystallization of a basaltic parent.  相似文献   

18.
Kohala revisited     
We present new isotopic data for Sr and Nd in basalts and alkalic volcanics from Kohala volcano, Hawaii, which had previously been described by Feigenson et al. (1983). These data complement our own isotopic data presented in that paper and those given in the companion paper by Lanphere and Frey (1986). We show that in spite of appearances to the contrary, there is no significant analytical bias in our previously published analyses. Accidental sampling bias and one erroneous value prevented us from recognizing the isotopic heterogeneity in our previously published data. The new data both confirm the Sr-isotopic distinction between Pololu and Hawi volcanics discovered by Lanphere and Frey and narrow the gap between them significantly. The two data sets agree for the Hawi samples, but the mean 87Sr/86Sr=0.703651±13 for our Pololu basalts is significantly lower than the mean 87Sr/86Sr= 0.703748±18 found by Lanphere and Frey. The Ndisotopic ratios are also heterogeneous, but they overlap for the two formations. We agree with the assessment of Lanphere and Frey that some of our samples originally classified as belonging to the Hawi Formation are actually derived from the uppermost Pololu Formation, but with some stratigraphic ambiguities remaining.We believe that our previous results of inverse modelling are valid for the tholeiitic and moderately alkalic Pololu Formation despite the isotopic heterogeneity because this heterogeneity does not correlate with the trace element chemistry of the Pololu samples.The severe depletion of Sc, which correlates with decreasing CaO/Al2O3 ratios and increasing Yb concentrations, confirms the importance of clinopyroxene fractionation in the evolved lavas of the Hawi Formation. In addition, apatite precipitation did fractionate the P/Ce ratios in the more evolved Hawi lavas, but its effect on the REE abundances is still uncertain and may not be significant.The MgO — P2O5 plot of Lanphere and Frey does not provide compelling evidence against a simple genetic relationship between Pololu and Hawi lavas. The internal consistency of the (fractionation corrected) trace element ratios such as Ba/Ce indicates that Ba is depleted in both the Hawi and the Pololu sources and that these sources do have similar chemistry.Finally, we show that contrary to the conclusions of Lanphere and Frey the REE patterns of Kohala volcanics can be generated from sources with only slightly negatively sloping REE patterns without involvement of garnet, as was indicated by the formal inversion analysis. Models which include garnet yield more highly anomalous source abundance patterns and calculated bulk-source partition coefficients which are inconsistent with the presence of garnet. The persistence of residual garnet is also inconsistent with the absence of significant heavy-REE fractionation among the Pololu basalts.  相似文献   

19.
At 39.5° S in the southern volcanic zone of the Andes three Pleistocene-recent stratovolcanoes, Villarrica, Quetrupillan and Lanin, form a trend perpendicular to the strike of the Andes, 275 to 325 km from the Peru-Chile trench. Basalts from Villarrica and Lanin are geochemically distinct; the latter have higher incompatible element abundances and La/Sm but lower Ba/La and alkali metal/La ratios. These differences are consistent with our previously proposed models involving: a) a west to east decrease in an alkali metal-rich, high Ba/La slab-derived component which causes an across strike decrease in degree of melting; or b) a west to east increase in the contamination of subduction-related magma by enriched subcontinental lithospheric mantle. Silicic and mafic lavas from the stratovolcanoes have overlapping Sr, Nd and O isotopic ratios. Silicic lavas also have geochemical differences that parallel those of their associated basalts, e.g., rhyolite from Villarrica has lower La/Sm and incompatible element contents than high-SiO2 andesite from Lanin. At each volcano the most silicic lavas can be modelled by closed system fractional crystallization while andesites are best explained by magma mixing. Apparently crustal contamination was not an important process in deriving the evolved lavas. Basaltic flows from small scoria cones, 20–35 km from Villarrica volcano have high incompatible element contents and low Ba/La, like Lanin basalts, but trend to higher K/Rb (356–855) and lower 87Sr/ 86Sr (0.70361–0.70400) than basalts from either stratovolcano. However all basalts have similar Nd, Pb and O isotope ratios. The best explanation for the unique features of the cones is that the sources of SVZ magmas, e.g., slab-derived fluids or melts of the subcontinental lithospheric mantle, have varying alkali metal and radiogenic Sr contents. These heterogeneities are not manifested in stratovolcano basalts because of extensive subcrustal pooling and mixing. This model is preferable to one involving crustal contamination because it can account for variable Sr isotope ratios and uniform Nd and Pb isotope ratios among the basalts, and the divergence of the cones from across-strike geochemical trends defined by the stratovolcanoes.  相似文献   

20.
Volatiles and major elements in submarine glasses from Loihi seamount and Kilauea volcano. Hawaii were analyzed by high temperature mass spectrometry and the electron microprobe. Loihi glasses are subdivided into three groups: tholeiitic, transitional and alkali basalts. The glasses are evolved: Mg numbers range from 48–58. The alkalic lavas are the most evolved.Total volatiles range from 0.73 to 1.40 wt.%. H2O shows a positive linear correlation with K2O content [H2O = 0.83 (± .09) K2O + 0.08 (± .06)]. Concentrations of H2O are higher in the alkalic lavas, but Cl and F abundances are highly variable. Variations in ratios of incompatible elements (K2O, P2O5, H2O) indicate that each group was derived from a distinct source. CO2 contents range from 0.05 to 0.19 wt.% but show no systematic correlation with rock type or Mg #. A well-defined decrease in glass CO2 content with increasing vesicularity is shown by the alkalic lavas. CO2 may have been outgassed from the tholeiitic and transitional magmas prior to eruption during storage in a shallow magma chamber. Reduced carbon species (CO and CH4) were found in small amounts in most of the alkalic samples. Although the redox histories of Hawaiian lavas are poorly known, these new data indicate the presence of a reduced source for Loihi magmas.The Kilauea tholeiitic glasses are evolved (Mg # 48.3 to 55) and have higher H2O contents (av. 0.54 wt.%) than Loihi tholeiites (av. 0.42 wt.%) at the same Mg # (~55). Cl is distinctly lower in Kilauea glasses (0.01 wt.%) compared to Loihi glasses (0.09 wt.%). The data indicate significant source differences for the two volcanoes, consistent with results of other geochemical studies.Loihi tholeiites have distinctly higher 3He/4He ratios than Kilauea tholeiites and are the highest measured in submarine basalts (KURZ et al., 1983). These high ratios have been used to invoke a primitive source for Loihi basalts. The high Cl content of these basalts, the highest we have ever measured in submarine basalts, may be a fingerprint of this primitive source, as previously noted for Icelandic basalts (Schillinget al. 1980).  相似文献   

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