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1.
 Mohns Ridge lavas between 71 and 72°30′N (∼360 km) have heterogeneous compositions varying between alkali basalts and incompatible-element-depleted tholeiites. On a large scale there is a continuity of incompatible element and isotopic compositions between the alkali basalts from the island Jan Mayen and Mohns Ridge tholeiites. The variation in isotopes suggests a heterogeneous mantle which appears to be tapped preferentially by low degree melts (∼5%) close to Jan Mayen but also shows its signature much further north on Mohns Ridge. Three lava types with different incompatible element compositions [e.g. chondrite-normalized (La/Sm)N<1 to >2] occur in the area at 72°N and were generated from this heterogeneous mantle. The relatively depleted tholeiitic melts were mixed with a small degree melt from an enriched source. The elements Ba, Rb and K of the enriched melt were probably buffered in the mantle by residual amphibole or phlogopite. That such a residual phase is stable in this region of oceanic mantle suggests both high water contents and low mantle temperatures, at odds with a hotspot origin for Jan Mayen. Instead we suggest that the melting may be induced by the lowered solidus temperature of a “wet” mantle. Mohns MORB (mid ocean ridge basalt) and Jan Mayen area alkali basalts have high contents of Ba and Rb compared to other incompatible elements (e.g. Ba/La >10). These ratios reflect the signature of the mantle source. Ratios of Ce/Pb and Rb/Cs are normal MORB mantle ratios of 25 and 80, respectively, thus the enrichments of Ba and Rb are not indicative of a sedimentary component added to the mantle source but were probably generated by the influence of a metasomatizing fluid, as supported by the presence of hydrous phases during the petrogenesis of the alkali basalts. Geophysical and petrological models suggest that Jan Mayen is not the product of hotspot activity above a mantle plume, and suggest instead that it owes its existence to the unique juxtaposition of a continental fragment, a fracture zone and a spreading axis in this part of the North Atlantic. Received: 3 May 1995 / Accepted: 6 November 1995  相似文献   

2.
Vesteris Seamount is a solitary alkaline volcano in the GreenlandBasin some 280 km NW of Jan Mayen. Topographic and geophysicalstudies have shown no sign of an associated plume trace. Evidencefrom ash layers in sediment cores around the volcano and datingof dredged samples show that it has been active in Quaternarytimes. The lavas from Vesteris studied here consist of basanites,tephrites, mugearite, and alkali basalts. Crystal fractionationmodels are consistent with the generation of the tephrites andmugearite from a basanitic parent. Extensive kaersutite fractionationis required late in the fractionation sequence to produce theextreme mugearite composition. Na-Al-Fe-rich green cores tomany clinopyroxene phenocrysts at Vesteris suggest a fractionationhistory beginning at high pressure in the mantle. Differencesbetween Vesteris and Jan Mayen in the ratios of highly incompatibletrace elements such as Ce/Pb and Rb/Cs, which will not normallybe fractionated from one another during mantle melting, suggestthat the two are not derived from the same source. Relativelyunradiogenic Sr isotope ratios (compared with Bulk Earth), andhighly incompatible trace element patterns similar to thosefor St. Helena, suggest that Vesteris magmas are derived froma depleted, asthenospheric source. We propose that the Vesterisbasanites are very low degree partial melts ({small tilde}1%)of this source, most probably those which give rise to the seismiclow-velocity zone (LVZ). Such small-degree melts may preferentiallytap small-scale heterogeneities in the asthenosphere. Vesterislies at the intersection of two major structural trends in theGreenland Basin—(1) a zone of major reorientation of spreadingdirection on the Mohns Ridge north of Jan Mayen and (2) theextension of the Kolbeinsey Ridge axis. We propose that a combinationof the extensional stress fields related to these two lineamentsproduces sufficient dilation of the lithosphere at Vesteristo allow magmas from the LVZ to reach the surface.  相似文献   

3.
Major element compositions of submarine basalts, quenched glasses, and contained phenocrysts are reported for samples from 25 dredge stations along the Mohns-Knipovich Ridge between the Jan Mayen fracture zone and 77°30N. Most of the basalts collected on the Jan Mayen platform have a subaerial appearance, are nepheline normative, rich in incompatible elements, and have REE-patterns strongly enriched in light-REE. The other basalts (with one exception) are tholeiitic pillow basalts, many of which have fresh quenched glass rims. From the Jan Mayen platform northeastwards the phenocryst assemblage changes from olivine±plagioclase±clinopyroxene±magnetite to olivine +plagioclase±chrome-spinel. This change is accompanied by a progressive decrease in the content of incompatible elements, light-REE enrichments and elevation of the ridge that are similar to those observed south of the Azores and Iceland hotspots. Pillow basalts and glasses collected along the esternmost part of the Mohns Ridge (450 to 675 km east of Jan Mayen) have low K2O, TiO2, and P2O5 contents, light-REE depleted patterns relative to chondrites, and Mg/(Mg+Fe2+) ratios between 0.64 and 0.60. Pillow basalts and glasses from the Knipovich Ridge have similar (Mg/Mg+Fe2+) ratios, but along the entire ridge have slightly higher concentrations of incompatible elements and chondritic to slightly light-REE enriched patterns. The incompatible element enrichment increases slightly northward. Plagioclase phenocrysts show normal and reverse zoning on all parts of the ridge whereas olivines are unzoned or show only weak normal zoning. Olivine-liquid equilibrium temperatures are calculated to be in the range of 1,060–1,206° C with a mean around 1,180° C.Rocks and glasses collected on the Jan Mayen Platform are compositionally similar to Jan Mayen volcanic products, suggesting that off-ridge alkali volcanism on the Jan Mayen Platform is more widespread than so far suspected. There is also evidence to suggest that the alkali basalts from the Jan Mayen Platform are derived from deeper levels and by smaller degrees of partial melting of a mantle significantly more enriched in light-REE and other incompatible elements than are the tholeiitic basalts from the Eastern Mohns and Knipovich Ridge. The possibility of the presence of another hitherto unsuspected enriched mantle region north of 77° 30 N is also briefly considered.It remains uncertain whether geochemical gradients revealed in this study reflect: (1) the dynamics of mixing during mantle advection and magma emplacement into the crust along the Mid-Atlantic Ridge (MAR) spreading axis, (e.g. such as in the mantle plume — large-ion-lithophile element depleted asthenosphere mixing model previously proposed); or (2) a horizontal gradation of the mantle beneath the MAR axis similar to that observed in the overlying crust; or (3) a vertical gradation of the mantle in incompatible elements with their contents increasing with depth and derivations of melts from progressively greater depth towards the Jan Mayen Platform.  相似文献   

4.
Compositionally, high-Nb basalts are similar to HIMU (high U/Pb) ocean island basalts, continental alkaline basalts and alkaline lavas formed above slab windows. Tertiary alkaline basaltic lavas from eastern Jamaica, West Indies, known as the Halberstadt Volcanic Formation have compositions similar to high-Nb basalts (Nb > 20 ppm). The Halberstadt high-Nb basalts are divided into two compositional sub-groups where Group 1 lavas have more enriched incompatible element concentrations relative to Group 2. Both groups are derived from isotopically different spinel peridotite mantle source regions, which both require garnet and amphibole as metasomatic residual phases. The Halberstadt geochemistry demonstrates that the lavas cannot be derived by partial melting of lower crustal ultramafic complexes, metasomatised mantle lithosphere, subducting slabs, continental crust, mantle plume source regions or an upper mantle source region composed of enriched and depleted components. Instead, their composition, particularly the negative Ce anomalies, the high Th/Nb ratios and the similar isotopic ratios to nearby adakite lavas, suggests that the Halberstadt magmas are derived from a compositionally variable spinel peridotite source region(s) metasomatised by slab melts that precipitated garnet, amphibole, apatite and zircon. It is suggested that high-Nb basalts may be classified as a distinct rock type with Nb > 20 ppm, intraplate alkaline basalt compositions, but that are generated in subduction zones by magmatic processes distinct from those that generate other intraplate lavas.  相似文献   

5.
The Marquesas Archipelago, a volcanic chain in French Polynesia (south-central Pacific Ocean), is predominantly composed of alkalic, transitional and tholeiitic basalts. The variation trends in these intraplate basaltic rocks imply that the magmas were derived from different upper mantle sources. Model calculations using the total inverse method show that the peridotite source of most Marquesas basalts was enriched in incompatible elements compared to a primordial mantle and had higher than chondritic ratios of several elements such as La/Yb, Ti/V and P/Ce. A metasomatic enrichment event is suggested by the sequence of element enrichment in the source relative to the primordial mantle (Ba>Nb>La>Ce>Sr>Sm>Eu> Zr>Hf>Ti>Y>Yb). On the other hand, some lavas including tholeiites of Ua Pou and alkalic basalts of Hiva Oa, were probably derived from relatively depleted upper mantle. In some islands such as Hatutu, the different types of basalts were generated from sources with rather similar compositions. The residual phases of the Marquesas magmas included garnet. The sources of these magmas were similar in trace element chemistry to the oceanic mantle below Hawaii.  相似文献   

6.
High precision Sr-Nd isotope ratios together with Pb isotope ratios corrected for mass fractionation using a double spike are reported for an extensive suite of late Quaternary to Recent lavas of Iceland, the Kolbeinsey and Reykjanes Ridges, and a small number of basalts from further south on the Mid-Atlantic Ridge. Compared with global MORB, the Icelandic region is distinguished by having low 207Pb/204Pb for any given 206Pb/204Pb, expressed by negative Δ207Pb (−0.8 to −3.5) in all but four Icelandic samples. Most samples also have elevated 208Pb/204Pb (strongly positive Δ208Pb), which combined with their negative Δ207Pb is very unusual in MORB worldwide. The negative Δ207Pb is interpreted as a consequence of evolution in high-μ mantle sources for the last few hundred Ma. The region of negative Δ207Pb appears to correspond with the region of elevated 3He/4He, suggesting that both lithophile and volatile elements in melts from the whole region between 56 and 70°N are dominantly sourced in a plume that has incorporated recycled Palaeozoic ocean crust and unradiogenic He, probably from the deep mantle. At least four mantle components are recognized on Iceland, two with an enriched character, one depleted and one that shows some isotopic affinities to EM1 but is only sampled by highly incompatible-element-depleted lavas in this study. Within restricted areas of Iceland, these components contribute to local intermediate enriched and depleted components that display near binary mixing systematics. The major depleted Icelandic component is clearly distinct in Pb isotopes from worldwide MORB, but resembles the depleted mantle source supplying the bulk of the melt to the Kolbeinsey and southern Reykjanes Ridges. However, an additional depleted mantle source is tapped by the northern Reykjanes Ridge, which with very negative Δ207Pb and less positive Δ208Pb is distinct from all Icelandic compositions. These components must mostly mix at mantle depths because a uniform mixture of three Icelandic components is advected southward along the Reykjanes Ridge.Despite strong covariation with isotope ratios, incompatible trace element ratios of Icelandic magmas cannot be representative of old mantle sources. The observed parent-daughter ratios in depleted and enriched Icelandic lavas would yield homogeneous Sr, Nd, Hf and 206Pb isotope signatures ∼170 Ma ago if present in their sources. The heterogeneity in 207Pb/204Pb is not however significantly reduced at 170 Ma, and the negative present day Δ207Pb cannot be supported by the low μ observed in depleted lavas from Iceland or the adjacent ridges. Since μ is higher in melts than in their sources, it follows that all the depleted sources must be residues from <170 Ma partial melting events. These are thought to have strongly affected most incompatible trace element ratios.  相似文献   

7.
Major and trace element compositions were obtained for bulk rocks and melt inclusions hosted in olivine crystals (Fo > 85) from the adventive cones of the Piton de La Fournaise volcano (La Réunion Island). Ratios of highly incompatible trace elements for these magmas are used to identify the nature of the La Réunion mantle plume source. Although adventive cone lavas display unusual major element compositions compared to the historical lavas of the volcano (e.g., lower CaO/Al2O3), trace element data suggest that the magmas emitted by the adventive cones originate from a common chemical source. This source may correspond to either a homogeneous mixed source of different mantle components or a near-primitive less-differentiated mantle source. The melt inclusions display ratios of highly incompatible elements (e.g., Th/La, Nb/La) which are similar to primitive mantle values, and lower Nb/U ratios compared to most oceanic basalts. These results and previous isotopic and trace element data suggest that La Réunion plume samples a source which is intermediate between a primitive-like mantle domain and a slightly depleted one almost unaffected by the recycling processes. This source could have originated from early depletion of the primitive mantle. Assuming a depletion 4.45 Gyr ago, ~10% melting of this slightly depleted source could explain the enriched trace element concentrations of the melt inclusions.  相似文献   

8.
The evolution of oceanic crust on the Kolbeinsey Ridge, north of Iceland, is discussed on the basis of a crustal transect obtained by seismic experiment from the Kolbeinsey Ridge to the Jan Mayen Basin. The crustal model indicates a relatively uniform structure; no significant lateral velocity variations are observed, especially in the lower crust. The uniform velocity structure suggests that the postulated extinct axis does not exist over the oceanic crust formed at the Kolbeinsey Ridge, but supports a model of continuous spreading along the ridge after oceanic spreading started west of the Jan Mayen Basin. The oceanic crust formed at Kolbeinsey Ridge is 1–2.5 km thicker than normal oceanic crust due to hotter-than-normal mantle from the Iceland Mantle Plume. The observed generally uniform thickness throughout the transect might also indicate that the temperatures of the astheno-spheric mantle ascending along the Kolbeinsey Ridge have not changed significantly since the age of magnetic anomaly 6B.  相似文献   

9.
New volatile data (CO2, H2O, He, Ne, and Ar) are presented for 24 submarine basaltic glasses from the Kolbeinsey Ridge, Tjörnes Fracture Zone and Mohns Ridge, North Atlantic. Low CO2 and He contents indicate that magmas were strongly outgassed with the extent of degassing increasing toward the south, as expected from shallower ridge depths. Ne and Ar are significantly more abundant in the southernmost glasses than predicted for degassed melt. The strong atmospheric isotopic signal associated with this excess Ne and Ar suggests syn- or posteruptive contamination by air. Degassing, by itself, cannot generate the large variations in δ13C values of dissolved CO2 or coupled CO2-Ar variations. This suggests that δ13C values were also affected by some other processes, most probably melt-crust interaction. Modelling indicates that degassing had a negligible influence on water owing to its higher solubility in basaltic melt than the other volatiles. Low H2O contents in the glasses reflect melting of a mantle source that is not water-rich relative to the source of N-MORB.Before eruption, Kolbeinsey Ridge melts contained ∼400 ppm CO2 with δ13C of −6‰, 0.1 to 0.35 wt.% H2O, 3He/4He ∼11 RA, and CO2/3He of ∼2 × 109. We model restored volatile characteristics and find homogeneous compositions in the source of Kolbeinsey Ridge magmas. Relative to the MORB-source, He and Ne are mildly fractionated while the 40Ar/36Ar may be low. The 3He/4He ratios in Tjörnes Fracture Zone glasses are slightly higher (13.6 RA) than on Kolbeinsey Ridge, suggesting a greater contribution of Icelandic mantle from the south, but the lack of 3He/4He variation along the Kolbeinsey Ridge is inconsistent with active dispersal of Icelandic mantle beyond the Tjörnes Fracture Zone.  相似文献   

10.
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   

11.
Tholeiitic basalts dredged from the Mid-Atlantic Ridge (MAR) axis at 43 ° N are enriched in incompatible trace elements compared to the ‘ normal’ incompatible element depleted tholeiites found from 49 ° N to 59 ° N and south of 33 ° N on the MAR. The most primitive 43 ° N glasses have MgO/FeO*= 1.2 and coexist with olivine (Fo90–91) and chrome-rich spinel. The tholeiitic basalts from the MAR 43 ° N are distinct from the strongly incompatible trace element depleted tholeiities found elsewhere in the Atlantic, and have trace element features typical of island tholeiities and MAR axis tholeiites from 45 ° N. Petrographic, major, and compatible trace element trends of the axial valley tholeiites at 43 ° N are consistent with shallow-level fractionation; in particular, evolution from primitive liquids with forsteritic olivine plus chrome spinel as liquidus phases to fractionated liquids with plagioclase plus clinopyroxene as major crystallizing phases. However, each dredge haul has distinctive incompatible trace element abundances. These trace element characteristics require a hetrogeneous mantle or complex processes such as open system fractional crystallization and magma mixing. Alkali basalts (～5% normative nepheline) were dredged from a prominent fracture zone at 43 ° N. Typical of alkali basalts they are strongly enriched (compared to tholeiites) in incompatible elements. Their highly fractionated rare-earth element (REE) abundances require residual garnet during partial melting. The 43 ° N tholeiites and alkali basalts could be derived from a garnet peridotite source with REE contents equal to 2 × chondrites by ～5% and 1% melting, respectively. Alternatively, they could be derived from a moderately light REE enriched source by ～25% and 9.5% melting, respectively.  相似文献   

12.
New 40Ar–39Ar ages of 5.6 to 1.3 Ma for lavas from the fossil Phoenix Ridge in the Drake Passage show that magmatism continued for at least 2 Ma after the cessation of spreading at 3.3 ± 0.2 Ma. The Phoenix Ridge lavas are incompatible element-enriched relative to average MORB and show an increasing enrichment with decreasing age, corresponding to progressively decreasing degrees of partial melting of spinel peridotite after spreading stopped. The low-degree partial melts increasingly tap a mantle source with radiogenic Sr and Pb but unradiogenic Nd isotope ratios implying an ancient enrichment. The post-spreading magmas apparently form by buoyant ascent of enriched and easily fusible portions of the upper mantle. Only segments of fossil spreading ridges underlain by such enriched and fertile mantle show post-spreading volcanism frequently forming bathymetric highs. The Phoenix Ridge lavas belong to the Pacific, rather than the Atlantic, mantle domain in regional Sr–Nd–Pb space. Our new data show that the southern Pacific Ocean mantle is heterogeneous containing significant enriched portions that are preferentially tapped at low melt fractions. Isotopic mapping reveals that Pacific-type upper mantle flows eastward through Drake Passage and surrounds the subducting Phoenix Plate beneath the Bransfield Basin.  相似文献   

13.
MORB suites display variations in their chemical differentiation trends which are closely related to the incompatible element enrichment of the basalts. We examine suites of primitive to evolved basalts from the Pacific-Nazca Ridge at 28° S (mostly depleted); from the Juan Fernandez microplate region (depleted) and from the Explorer Ridge, northeast Pacific (mostly enriched). Trends for incompatible element enriched MORBs consistently show less depletion of Al2O3 and less enrichment of FeO when plotted on MgO variation diagrams.Least squares modeling indicates that enriched basalts have undergone less plagioclase crystallization than depleted basalts especially in the early stages of differentiation. Using thermodynamic modelling, we show that variations between MORB differentiation trends result largely from differences in the major element chemistry and H2O content of primary magmas. Our chosen enriched and depleted near-primary magmas are similar in major element chemistry but the enriched near-primary magma has higher H2O and lower Al2O3 than the depleted near-primary magma. The MORB crystallization sequence is: olivineolivine+plagioclase olivine+plagioclase+high-Ca pyroxene; and the separate and combined effects of lower Al2O3 and higher H2O are to cause plagioclase to crystallize later (lower temperature), and to make the interval of olivine+plagioclase crystallization shorter. As a result, enriched differentiates have higher Al2O3 and lower FeO than depleted MORBs at a given MgO content, even though their parents' Al2O3 is lower. Crystallization of enriched basalts at higher pressure than depleted basalts is not able to account for differences between the differentiation trends because the proportion of plagioclase is higher during three-phase crystallization at high pressure.The variations in trends do not depend on geographic location and thus are superimposed on any regional variations in MORB chemistry or mantle source. Nor are they related to spreading rate. Depleted basalts from the fast-spreading 28° S and Juan Fernandez ridges have differentiation trends similar to depleted basalts from the medium-spreading Galapagos Spreading Center, whereas differentiation trends for enriched basalts from the medium-spreading Explorer Ridge are quite different. Fe3+/Fetotal is similar (and quite low) for enriched and depleted basalts, indicating that neither oxidation state nor early magnetite crystallization are important.  相似文献   

14.
The development of petrogenetic models of igneous processes in the mantle is dependent on a detailed knowledge of the diversity of magmas produced in the melting regime. These primary magmas, however, undergo significant mixing and fractionation during transport to the surface, destroying much of the evidence of their primary diversity. To circumvent this problem and to determine the diversity of melts produced in the mantle, we used melt inclusions hosted in primitive plagioclase phenocrysts from eight mid-ocean ridge basalts from the axial and West Valleys of the Endeavour Segment, Juan de Fuca Ridge. This area was selected for study because of the demonstrated close association of enriched (E-MORB) lavas and incompatible element enriched depleted (N-MORB) lavas. Rehomogenized melt inclusions from E-MORB, T-MORB, and N-MORB lavas have been analyzed by electron and ion microprobe for major and trace elements. The depleted and enriched lavas, as well as their melt inclusions, have very similar compatible element concentrations (major elements, Sr, Ni and Cr). Inclusion compositions are more primitive than, yet collinear with, the host lava suites. In contrast, the minor and trace element characteristics of melt inclusions from depleted and enriched lavas are different both in range and absolute concentration. N-MORB lavas contain both depleted and enriched melt inclusions, and therefore exhibit the largest compositional range (K2O: 0.01 to 0.4 oxide wt%, P2O5: <0.01 to 0.2 oxide wt%, LaN: 7 to 35, YbN: 1 to 13, and Ti/Zr: <100 to 1300). E-MORB lavas contain only enriched inclusions, and are therefore relatively homogeneous (K2O: 0.32 to 0.9 oxide wt %, P2O5: 0.02 to 0.35 oxide wt%, LaN: 11 to 60, YbN: 4 to 21, and Ti/Zr: ∼100). In addition, the most primitive E-32 inclusions are similar in composition to the most enriched inclusions from the depleted hosts. Major element data for melt inclusions from both N-MORB and E-MORB lavas suggest that the magmas lie on a low pressure cotectic, consistent with a petrogenesis including fractional crystallization. However, the minor and trace element compositions in melt inclusions vary independently of the major element composition implying an alternative history. When fractionation-corrected, inclusion compositions correlate with their host glass composition. Hence, the degree of enrichment of the lavas is a function of the composition of aggregated melts, not of processing in the upper mantle or lower crust. Based on this fact, the lava suites are not produced from a single parent magma, but from a suite of primary magmas. The chemistry of the melt inclusions from the enriched lavas is consistent with a derivation from variable percentages of partial melting within the spinel stability field by a process of open system (continuous or critical) melting assuming a depleted lherzolite source veined with clinopyroxenite. The low percentage melts are dominantly enriched melts of the clinopyroxenite. In contrast, the depleted lavas were created by melting of a harzburgite source, possibly fluxed with a fluid enriched in K, Ba and the LREE. Such a source was likely melted up to or past the point at which all of its clinopyroxene was consumed. This set of characteristics is consistent with a scenario by which diverse melts produced at different depths travel through the melting regime to the base of the crust without homogenizing en route. The homogeneous major element characteristics are created in the lower crust by fractional crystallization and reaction with lower crustal gabbros. Therefore, the degree of decoupling between major and trace element characteristics of the melt inclusions (and lavas) is dictated by the reaction rate of the melts with the materials in the conduit walls, as well as the residence times and flux rate, in the upper mantle and lower crust. Received: 2 December 1997 / Accepted: 27 August 1998  相似文献   

15.
Late Archaean komatiitic lavas from Newton Township, Ontario, consist of 6 chemically distinct magma types: 3 komatiites and 3 komatiitic basalts. The succession is unusual in containing both Al- and HREE-depleted komatiites and Al- and HREE-undepleted komatiites. The two types form distinct stratigraphic units separated by komatiitic basalts. Two komatiite types are strongly LREE depleted, whilst the third and the associated komatiitic basalts range from mildly depleted to enriched. Of the six magma types, only the two strongly LREE depleted komatiites represent primary mantle melts. The other komatiite type and the komatiitic basalts were derived from the primary komatiite magmas by combinations of olivine (+chromite) fractionation, assimilation of continental crust, and magma mixing. The two primary magmas may have been derived from similar sources, their contrasting chemistry being due to differing degrees of garnet segregation during melting. A generally applicable conclusion is that a wide range of komatiitic magma types can be generated from a relatively homogeneous depleted mantle, under conditions likely to prevail during the eruption of late Archean greenstone belt sequences.  相似文献   

16.
New measurements of Os, He, Sr and Nd isotopes, along with major and trace elements, are presented for basalts from the three volcanic flank zones in Iceland and from Jan Mayen Island. The 187Os/188Os ratios in lavas with <30 ppt Os (n = 4) are elevated compared to ratios in coexisting olivine and appear to be contaminated at a shallow level. The 187Os/188Os ratios in the remaining lavas with >30 ppt Os (n = 17) range between 0.12117 and 0.13324. These values are surprisingly low for oceanic island basalts and include some samples that are less than putative present-day primitive upper mantle (PUM with 187Os/188Os of 0.1296). These low 187Os/188Os preclude significant shallow-level contamination from oceanic crust. The 187Os/188Os ratios for Jan Mayen lavas are less than PUM, severely limiting the presence of any continental crust in their mantle source. A positive correlation between 143Nd/144Nd and 187Os/188Os ratios in Iceland and Jan Mayen lavas likely reflects the presence in their source of ancient subcontinental lithosphere that has undergone incompatible trace element enrichment that did not affect the Re-Os system. In addition, the Jan Mayen lava isotopic signature cannot be explained solely by the presence of subcontinental lithospheric mantle, and the influence of another geochemical component, such as a mantle plume appears required. Combined 87Sr/86Sr, 143Nd/144Nd, 3He/4He and 187Os/188Os data indicate a genetic relationship between Jan Mayen Island and the Iceland mantle plume. Material from the Iceland mantle plume likely migrates at depth until it reaches the tensional setting of the Jan Mayen Fracture Zone, where it undergoes low-degree partial melting. At a first-order, isotopic co-variations can be interpreted as broadly binary mixing curves between two primary end-members. One end-member, characterized in particular by its unradiogenic 187Os/188Os and 143Nd/144Nd, low 3He/4He and high 87Sr/86Sr, is represented by subcontinental lithospheric mantle stranded and disseminated in the upper mantle during the opening of the Atlantic Ocean. The second end-member corresponds to a hybrid mixture between the depleted-MORB mantle and the enriched Iceland mantle plume, itself resulting from mixing between recycled oceanic crust and depleted lower mantle. This hybrid accounts for the high 3He/4He (∼28 Ra), high 143Nd/144Nd (∼0.5132), high 187Os/188Os (∼0.14) and low 87Sr/86Sr (∼0.7026) composition observed in Iceland. Two different models may account for these observed mixing relationships between the end-members. In this first model, the Iceland mantle entrains pristine depleted material when rising in the upper mantle and allows refractory sub-lithospheric fragments to melt because of excess heat derived from the deep plume material. A second model that may better account for the Pb isotopic variations observed, uses the same components but where the depleted-MORB mantle is already polluted by subcontinental lithospheric mantle material before mixing with the Iceland mantle plume. Both cases likely occur. Though only three principal components are required to explain the isotopic variations of the Iceland-Jan Mayen system, the different possible mixing relationships may be accounted for by potentially a greater number of end-members.  相似文献   

17.
 The use of ocean floor basalt chemistry as a tool to investigate mantle composition and processes requires that we work with basalts that have been modified little since leaving the mantle. One source of such basalts is melt inclusions trapped in primitive crystals. However, obtaining information from these melt inclusions is complicated by the fact that melt inclusions in natural basalts are essentially always altered by post-entrapment crystallization. This requires that we develop techniques for reconstructing the original trapped liquid compositions. We conducted a series of experiments to reverse the effects of post-entrapment crystallization by re-heating the host crystals to their crystallization temperature. For these experiments we used plagioclase crystals separated from a single Gorda Ridge lava. The crystallization temperature for these crystals was determined by a set of incremental re-heating experiments to be ∼1240–1260° C. The inclusions are primitive, high Ca-Al basaltic melts, saturated with plagioclase, olivine and Al-rich chromite at low pressure. The inclusion analyses can be linked to the host lava composition by low pressure fractionation. The major element composition of the re-homogenized melt inclusions within each crystal is relatively constant. However, the incompatible element analyses have extremely wide ranges. The range of La/Sm and Ti/Zr from inclusions analyzed from a single sample from the Gorda Ridge exceeds the range reported for lavas sampled from the entire ridge. The pyroxene compositions predicted to be in equilibrium with the melt inclusion trace element signature cover much of the range represented by pyroxenes from abyssal peridotites. The volumetric proportions of the magmas entering the base of the crust can be evaluated using frequency distribution of melt inclusion compositions. This distribution suggests that the array of magmas was skewed towards the more depleted compositions, with little evidence for an enriched component in this system. This pattern is more consistent with a dynamic flow model of the mantle or of a passive flow model where the melts produced in the peripheral areas of the melting regime were not focused to the ridge. Received: 5 January 1995 / Accepted: 13 June 1995  相似文献   

18.
峨眉山大火成岩省：地幔柱活动的证据及其熔融条件   总被引：138，自引：5，他引：138  
对苦橄岩中橄榄石斑晶及其中熔体包裹体的电子探针分析表明，峨眉山大火山岩省的原始岩浆具高镁（ MgO > 16％）特征。玄武岩的 REE反演计算揭示，参与峨眉山玄武岩岩浆作用的地幔具有异常高的潜能温度（ 1 550℃）。这些特征以及峨眉山玄武岩的大面积分布和一些熔岩所显示的类似于洋岛玄武岩 (OIB)的微量元素和 Sr- Nd同位素特征均为地幔热柱在能量和物质上参与峨眉山溢流玄武岩的形成提供了确凿证据。峨眉山两个主要岩类（高钛和低钛玄武岩）可能是不同地幔源区物质在不同条件下的熔融产物。低钛玄武岩形成于温度最高、岩石圈最薄的地幔柱轴部。地幔（ ISr≈ 0.705,ε Nd(t)≈＋ 2）熔融始于 140 km，并一直延续到较浅的深度（ 60 km,尖晶石稳定区 ),部分熔融程度为 16％，这类岩石可能代表了峨眉山玄武岩的主体。而高钛玄武岩的母岩浆的形成基本局限在石榴子石稳定区（ > 70 km），其源区特征为 : ISr≈ 0.704,ε Nd(t)≈＋ 5，可能代表了热柱边部或消亡期地幔小程度部分熔融（ 1.5％）的产物。  相似文献   

19.
Petrological and geochemical data obtained on the Quaternary lavas of volcanoes at Spitsbergen Island indicate that the rocks were produced via the deep-seated crystallization of parental alkaline magmas at 8–10 kbar. The character of clinopyroxene enrichment in incompatible elements indicates that the mineral crystallized from more enriched melts than those inferred from the composition of the host lavas. These melts were close to the parental melts previously found as veinlets in mantle hyperbasite xenoliths in the lavas. According to the character of their enrichment in Pb and Sr radiogenic isotopes and depletion in Nd, the basalts from Spitsbergen Island define a single trend with the weakly enriched tholeiites of the Knipovich Ridge, a fact suggesting the closeness of the enriched sources beneath the continental margin of Spitsbergen and beneath the spreading zone. Magmatic activity at Spitsbergen was related to the evolution of the Norwegian-Greenland basin, which evolved in pulses according to the shift of the spreading axes. The most significant of the latter events took place in the Neogene, when the Knipovich Ridge obtained its modern position near the western boundary of Spitsbergen. Early in the course of the evolution, the emplacement of alkaline melts generated at Spitsbergen into the oceanic mantle could form the enriched mantle, which was later involved in the melting process beneath the spreading zone.  相似文献   

20.
The main plutonic complex of the Troodos ophiolite, north of the Arakapas Fault Zone, has been re-examined both from field and geochemical perspectives. Ion microprobe analyses of clinopyroxene crystal cores show that the range of melt compositions added to the lower crust far exceeds that of published lavas in the main Troodos massif. This suggests that the lower crust acted as a filter into which a large range of melt compositions were added and out of which a homogenised (and generally fractionated) derivative was extracted. This crustal-level aggregation homogenised diverse melt fractions from a broad range of degrees of melting. Depleted melts with U-shaped rare earth element (REE) patterns were a significant component of the melts added to the crust, but because of their low incompatible element abundances, mixing with less depleted melts prior to eruption masked their signature in the lavas. The discovery that highly depleted melts constituted a significant component of the melts added to the Troodos crust, but not of the lavas, demonstrates that the spatial distribution of lava-types is not necessarily a good indicator of where different parental melt compositions are generated within the mantle. Compared with normal mid-ocean ridge basalts, the Troodos parental melts were (1) generally depleted in immobile incompatible trace elements, (2) less depleted in light REE (LREE) than would be expected for the concomitant depletion in middle and heavy REE, (3) enriched in Sr with respect to the LREE and (4) more oxidised. Modelling of these characteristics suggests a mantle source that had previously lost a significant melt fraction under relatively reducing conditions. This was followed by remelting under more oxidising conditions in an environment in which Sr and LREE were added to the source consistent with previous models of a supra-subduction zone setting.  相似文献   

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