Geochemistry and Petrology of Emeishan Basalts and Subcontinental Mantle Evolution in Southwestern China

Three major volcanic rock sequences in the P2β formation(Emeishan basalts)were sampled dur-ing a comprehensive study of the Late Permian volcanics associated with the Panxi paleorift in southwestern China .Two of the three sections-Emei and Tangfang are composed of continental flood basalts(CFB) while the third-Ertan is an alkalic center.Multi-element chemical analyses indi-cate a predominance of low MgO transitional quartz tholeiites at Emei and Tangfang,whereas the Ertan suite ranges from high-MgO alkaline olivine basalts to rhombic porphyry trachytes and quartz-bearing aegerine-augite syenites.Consanguineity of the rocks from the three sections is sug-gested by consistently high TiO2 ,K2O,incompatible trace elements and uniformly fractionated REE patterns typical of alkalic compositions,but antypical of CFB.Sr isotope data for ten Emei basalt samples(^87Sr/^86Sr=0.7066-0.7082)which show no correla-tion with Rb/Sr ratios (0.02-0.12) and Nd isotopes for two of the samples(^143Nd/^144Nd=0.51171-0.51174)are interpreted as being related to the mantle evolution.The primary magmas re-sponsible for all the three sequences have been modeled in terms of a uniformly metasomatized man-tle source.Trace element models support the derivation of the Emei and Tangfang primary magmas from 10-15 percent partial melting of spinel lherzolite,followed by fractional crystallization of olivive and clinopyroxene.The primary alkaline olivine basalts at Ertan are generated by 7-10 percent par-tial melting of a chemically equivalent source in the garnet-peridodite stability region.The assumed mantle composition is characterixzed by Rb=3.8-5.5 ppm,Sr=62-83ppm,Ba=45-64 ppm,La=3.8-5.6ppm,and Yb=0.46-0.57ppm.The proposed mechanism of regional mantle enrichment requires metasomatic stabilization of phlogopite which becomes depleted later during par-tial melting.Such enrichment is consistent with the models proposed for alkalic systems in which a large mantle diaper acts as the agent for upward enrichment as well as uplift and extension of the crust.     

Geochemistry of basic dikes in the Lanzo massif (Western Alps): Petrogenetic and geodynamic implications

The Alpine peridotite massif of Lanzo (Italy) contains three generations of basic dikes (gabbros and basalts). The older gabbros are plagioclase-rich mantle segregates while the younger gabbro dikes are cumulates very similar in chemical composition to recent oceanic gabbros and gabbros from ophiolitic complexes. They both were derived from the N-type mid-ocean ridge basalt (MORB) magmas which were progressively more depleted in incompatible elements and were probably generated during a dynamic melting of a rising mantle diapir. The basaltic dikes are the N-type MORB and closely resemble the Alpine-Apennine ophiolitic basalts. They were derived from a different upper mantle source than the parental magmas of the gabbros. The source of the basalts was less depleted in light REE. The presence of basic magmas with N-type MORB affinities in the Lanzo massif is consistent with the close genetic relationship between the Alpine peridotite body and the ophiolites of the Liguro-Piemontese basin.     

Constraints on the origin of alkaline and calc-alkaline magmas from the Tuxtla Volcanic Field,Veracruz, Mexico

 Lavas erupted in the Tuxtla Volcanic Field (TVF) over the last 7 Ma include primitive basanites and alkali basalts, mildly alkaline Hy-normative mugearites and benmoreites, and calc-alkaline basalts and basaltic andesites. The primitive lavas are silica-undersaturated, with high concentrations of both incompatible and compatible trace elements, variable La/Yb with constant Yb at 6 to 8 times chondritic, and low Sr and O and variable Pb and Nd isotopic ratios. The primitive magmas originated by increasing degrees of melting with pressure decreasing from greater than 30 kbar to 20 kbar, in the garnet stability field. Another group of alkali basalts and hawaiites has lower Ni and Cr concentrations and higher Fe/Mg ratios, and was derived from the primitive group by crystal fractionation at pressures of several kbar. Incompatible trace elements in these silica undersaturated lavas show depletion in high field strength elements (HFSE) relative to large ion lithophile elements, similar to subduction-related basalts. Ba/Nb ratios are nearly constant and thus the HFSE depletion cannot be the result of a residual HFSE-bearing phase in the source, but could be the result of generation from a source contaminated by fluids or melts from the subducted lithosphere. The silica-saturated mugearites and benmoreites, and the calc-alkaline basalts and basaltic andesites, were erupted only between 3.3 and 1.0 Ma. These have incompatible element concentrations generally lower than in the silica-undersaturated lavas, and thus could not have been derived by crystal fractionation from the silica-undersaturated alkaline magmas. Magmas parental to the silica-saturated magmas originated by higher degrees of melting at lower pressures than the primitive magmas. Melting may have been promoted by an influx of fluid from the subducted lithosphere. Trace element and Sr, Nd, Pb and O isotopic data suggest that three components are involved in the generation of TVF magmas: the mantle, a fluid from the subducted lithosphere, and continental crust. TVF alkaline lavas are similar to those erupted in the back-arc region of the MVB and Japan, and show characteristics similar to alkaline magmas erupted in the southern Andean volcanic arc. These low degree melts reach the surface along with calc-alkaline lavas in the TVF due to an extensional stress field that allows their passage to the surface. Received: 15 September 1994/Accepted: 14 February 1995     

The systematics of lithium abundances in young volcanic rocks

Lithium is a moderately incompatible trace element in magmatic systems. High precision analyses for lithium conducted on well characterized suites of MORB and ocean island basalts suggest a bulk distribution coefficient of 0.25−0.35 and behavior which is similar to Yb during low pressure fractionation and V during melting, as long as garnet is not an important residual phase. Data for peridotites and basalts suggest a mantle lithium content of about 1.9 ppm and show that significant concentrations of lithium reside in olivine and orthopyroxene, resulting in unusual inter-mineral partitioning of Li and complex relationships between lithium and other incompatible trace elements.The lithium abundances of arc basalts are similar to those of MORB, but their Li/Yb ratios are considerably higher. The high Li/Yb suggests the addition of a Li-rich component to arc sources; relatively low Yb abundances are consistent with the derivation of some arc magmas by larger extents of melting or from a more depleted source than MORB. Although Li is enriched at arcs, K is enriched more, leading to elevated K/Li ratios in arc volcanics. The high K/Li and relatively low La/Yb of primitive arc basalts requires either incorporation of altered ocean crust into arc magma sources, or selective removal of K and Li from subducted sediments. Bulk incorporation of sediments alone does not explain the Li systematics.Data from primitive MORB indicate a relatively low (3–4 ppm) Li content for new oceanic crust. Thus, the Li flux from the ocean crust is probably <1 × 10¹¹ g/yr, and the oceanic crust may not be an important net source in the oceanic budget of lithium.     

中国东北软流圈地幔中的原始橄榄岩质地幔:来自大兴安岭地区新生代玄武岩的地球化学证据

为了进一步了解中国东北新生代玄武岩地幔源区的物质属性,报道了大兴安岭哈拉哈河-柴河地区新生代玄武岩的全岩主量、微量元素和Sr、Nd、Pb、Hf同位素组成.哈拉哈河-柴河玄武岩属钠质碱性系列,具有与洋岛玄武岩相似的微量元素特征,如富集大离子亲石元素（LILEs）、明显的Nb、Ta正异常等.它们具有中等亏损的Sr-Nd-Hf同位素组成（87Sr/86Sr=0.703 5~0.703 9、ε_Nd=5.21~6.55、ε_Hf=10.00~11.25）,接近中国东部新生代玄武岩的亏损端元.这些玄武岩具有中等的放射成因Pb同位素组成（206Pb/204Pb=18.37~18.57、207Pb/204Pb=15.52~15.54和208Pb/204Pb=38.24~38.43）,在206Pb/204Pb-207Pb/204Pb相关图上位于4.42~4.45 Ga的地球等时线之间.它们在Sr-Nd-Pb同位素相关图中均落入地幔柱来源的、高3He/4He比（>30R_a）的洋岛玄武岩范围内,暗示其源区可能存在来自深部地幔的古老原始地幔物质.此外,这些玄武岩具有高MgO（8.49%~11.58%）、高Ni（174×10-6~362×10-6）和高Mg#（59.1~66.9）的特征,表明它们接近于原始岩浆的成分.反演的哈拉哈河-柴河玄武岩的原始岩浆组成具有中等的SiO₂、低Al₂O₃以及高CaO/Al₂O₃比的特征,与石榴子石橄榄岩高压（>2.5 GPa）实验熔体的成分相当,暗示玄武岩的源区岩性最可能为橄榄岩.对以原始地幔（而不是亏损地幔）的微量元素为初始成分的饱满石榴子石二辉橄榄岩进行低程度（1%~2%）部分熔融的模拟计算,产生的熔体与哈拉哈河-柴河玄武岩具有一致的微量元素特征,这进一步支持了上述推断.综上所述,认为大兴安岭地区哈拉哈河-柴河玄武岩的源区含有来自深部地幔的古老的橄榄岩质原始地幔组分.      

Mineralogy,geochemistry and petrogenesis of Kurile island-arc basalts

Whole-rock (major- and trace-element) and mineral chemical data are presented for basaltic rocks from the main evolutionary stages of the Kurile island arc, NW Pacific. An outer, inactive arc contains a Cretaceous-Lower Tertiary sequence of tholeiitic, calcalkaline and shoshonitic basalts. The main arc (Miocene-Quaternary) is dominated by weakly tholeiitic, with lesser, alkalic basalts. The mineralogy of Kuriles basalts is characterised by An-rich plagioclases, a continuous transition from chromites to titanomagnetites, pyroxenes with low Fe³⁺ contents and without strong Fe-enrichment, abundance of groundmass pigeonites and the absence of amphiboles. There is an increase in K₂O contents both along-arc (northwards) and towards the reararc side. The basalts show an exceptionally wide but continuous range of K₂O contents (0.1–4.7%) which correlate with other LIL element contents. Tholeiitic basalts with low LIL element contents, La/Yb and Th/U, but high K/ Rb, P₂O₅/La and Zr/Nb were derived from depleted, lherzolitic mantle which had suffered fluid metasomatism by K, Rb, Cs, Sr, Ba, Pb and H₂O only. Alkali basalts are also thought to be derived from depleted mantle but melt metasomatism involved addition of all LIL elements to a garnet lherzolite mantle. The Kuriles basalts and their mantle sources range continuously between these two end-member compositions. The metasomatic fluids/melts were probably released by early dehydration and later melting within subducted oceanic lithosphere though the process is not adequately constrained.     

Elemental and Sr isotope variations in basic lavas from Iceland and the surrounding ocean floor

Major and trace element data are used to establish the nature and extent of spatial and temporal chemical variations in basalts erupted in the Iceland region of the North Atlantic Ocean. The ocean floor samples are those recovered by legs 38 and 49 of the Deep Sea Drilling Project. Within each of the active zones on Iceland there are small scale variations in the light rare earth elements and ratios such as K/Y: several central complexes and their associated fissure swarms erupt basalts with values of K/Y distinct from those erupted at adjacent centres; also basalts showing a wide range of immobile trace element ratios occur together within single vertical sections and ocean floor drill holes. Although such variations can be explained in terms of the magmatic processes operating on Iceland they make extrapolations from single basalt samples to mantle sources underlying the outcrop of the sample highly tenuous. ⁸⁷Sr/86Sr ratios measured for 25 of the samples indicate a total range from 0.7028 in a tholeiite from the Reykjanes Ridge to 0.7034 in an alkali basalt from Iceland and are consistent with other published ratios from the region. A positive correlation between ⁸⁷Sr/⁸⁶Sr and Ce/Yb ratios indicates the existence of systematic isotopic and elemental variations in the mantle source region. An approximately fivefold variation in Ce/Yb ratio observed in basalts with the same ⁸⁷Sr/⁸⁶Sr ratio implies that different degrees and types of partial melting have been involved in magma genesis from a single mantle composition. ⁸⁷Sr/⁸⁶Sr ratios above 0.7028, Th/U ratios close to 4 and La/Ta ratios close to 10 distinguish most basalts erupted in this part of the North Atlantic Ocean from normal mid-ocean ridge basalt (N-type MORE) — although N-type MORB has been erupted at extinct spreading axes just to the north and northeast of Iceland as well as the presently active Iceland-Jan Mayen Ridge.Comparisons with the hygromagmatophile element and radiogenic isotope ratios of MORB and the estimated primordial mantle indicate that the mantle sources producing Iceland basalts have undergone previous depletion followed by more recent enrichment events. A veined mantle source region is proposed in preference to the mantle plume model to explain the chemical variations.     

Magmatic processes and mantle heterogeneity beneath the slow-spreading northern Kolbeinsey Ridge segment,North Atlantic

We present new data on mineralogical, major and trace element compositions of lavas from the northernmost segment of the Kolbeinsey Ridge (North Kolbeinsey Ridge, NKR). The incompatible element enriched North Kolbeinsey basalts lie on a crystal fractionation trend which differs from that of the other Kolbeinsey segments, most likely due to higher water contents (~0.2%) in the NKR basalts. The most evolved NKR magmas erupt close to the Jan Mayen Fracture Zone, implying increased cooling and fractionation of the ascending magmas. Mainly incompatible element-enriched basalts, as well as some slightly depleted lavas, erupt on the NKR. They show evidence for mixing between different mantle sources and magma mixing. North Kolbeinsey Ridge magmas probably formed by similar degrees of melting to other Kolbeinsey basalts, implying that no lateral variation in mantle potential temperature occurs on the spreading axis north of the Iceland plume and that the Jan Mayen Fracture Zone does not have a cooling effect on the mantle. Residual garnet from deep melting in garnet peridotite or from enriched garnet pyroxenite veins does not play a role. The incompatible element-enriched source has high Ba/La and Nb/Zr, but must be depleted in iron. The iron-depleted mantle is less dense than surrounding mantle and leads to the formation of the North Kolbeinsey segment and its shallow bathymetry. The enriched NKR source formed from a relatively refractory mantle, enriched by a small degree melt rather than by recycling of enriched basaltic crust. The depleted mantle source resembles the mantle of the Middle Kolbeinsey segment with a depletion in incompatible elements, but a fertile major element composition.     

The Stonyford Volcanic Complex: a Forearc Seamount in the Northern California Coast Ranges

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     

Petrogenesis of post-collisional Middle Eocene volcanism in the Eastern Pontides (NE,Turkey): Insights from geochemistry,whole-rock Sr-Nd-Pb isotopes,zircon U-Pb and 40Ar-39Ar geochronology

The debate about whether Eocene magmatism is considered to be post-collisional or subduction-related or not still continues. Here we offer new ⁴⁰Ar-³⁹Ar ad U-Pb zircon geochronology, mineral chemistry, bulk rock and Sr-Nd-Pb isotope geochemistry data obtained from the southern dike (SD) suite, in comparison with the northern dike (ND) suite, from the Eastern Pontides. The geochronological data indicate that the SD suite erupted between 45.89 and 45.10 Ma corresponding to the Lutetian (Middle Eocene). The magmas of the ND suite are characterised by slightly more alkaline affinity compared to the SD suite. The trace and rare earth element (REEs) content of the SD suite is characterised by large ion lithophile element (LILEs; Sr, K₂O, Ba, Rb) enrichment and depletion of Nb, Ta, and TiO₂ elements to different degree with high Th/Yb ratios, which indicate that the magmas forming the SD and ND suites were derived from lithospheric mantle sources enriched by mostly slab-derived fluids in the spinel stability field. The Sr, Nd and Pb radiogenic isotope ratios of the dikes support the view that the magma for the hydrous group (H-SD) was derived from a relatively more enriched mantle source than the other SD and ND suites. The ND suite and the anhydrous group (A-SD) display similar geochemical features characterised by moderate light earth element (LREE)/heavy rare earth element (HREE) ratios, while the H-SD group has respectively lower LREE/HREE ratios indicating higher melting degree. Detailed considerations of the alkalinity, enrichment and partial melting degree for the source of the studied volcanic rocks indicate that the magmas of the northern dike suite are characterised by slightly more alkaline affinity, whereas the magmas throughout the southern dike suite show increments in the enrichment rate and melting degree. In light of the obtained data and comparative interpretations, the geodynamic evolution and differences in petrogenetic character of the Lutetian magmas from both the northern and southern parts of the Eastern Pontides may be explained by different degrees of melting of a net veined mantle source initially metasomatized by mostly subduction fluids during asthenospheric upwelling due to fragmented asymmetric delamination in a post-collisional extensional tectonic environment.     

Origin of high field strength element enrichment in volcanic arcs: Geochemical evidence from the Sulu Arc, southern Philippines

Lavas from the Sulu Arc, southern Philippines, exhibit an enrichment in high field strength elements (HFSE) that represents a departure from the typical volcanic arc geochemical signature. It has been postulated that this relative enrichment arises from metasomatism of mantle wedge peridotites by melts derived from the subducting oceanic lithosphere, through formation of amphibole which subsequently breaks down and enriches the mantle source of parental arc magmas in HFSE. Divergent chemical and isotopic characteristics between Sulu Arc HFSE-enriched lavas and the Sulu Sea crust being subducted—the presumed source of slab-derived melts—render it unlikely, however, that HFSE enrichment arises from the influence of such melts. New geochemical data suggest that the varying degrees of HFSE enrichment in Sulu Arc lavas are instead the result of variable amounts of mixing between enriched and depleted mantle end-components—the sources of South China Sea intraplate lavas and Sulu seafloor basalts, respectively—within a compositionally heterogeneous mantle wedge.     

Magmatic evolution of the Karmøy Ophiolite Complex,SW Norway: relationships between MORB-IAT-boninitic-calc-alkaline and alkaline magmatism

The polyphasal magmatic evolution of the Caledonian Karmøy Ophiolite Complex includes: (1) formation of an axis sequence from island-arc tholeiitic (IAT) and more MORB-like magmas (493+7/-4 Ma); (2) intrusion of magmas of boninitic affinity (485±2 Ma); (3) intrusion of MORB- and IAT-like magmas; (4) intrusion and extrusion of calc-alkaline magmas (470+9/-5 Ma); (5) intrusion and extrusion of basalts with alkaline trace-element affinity. Repeated intrusion of MORB and IAT-like magmas may be explained by intermittent magmatism involving magma-chamber solidification and remelting of a source characterized by initial _Nd of approximately +6.5. The boninitic rocks may have formed from two LREE-depleted sources: the primary source of the axis-sequence magmas and the residual source left after extraction of these magmas. These sources have been enriched in LREE, Th and Zr from subducted material exhibiting a continental Nd-isotope signature with initial _Nd less than-8. Covariation between _Nd and Th, Zr, Nd, Y and Yb may be explained by metasomatic enrichment of a LREE-depleted mantle source by a LREE-enriched subduction component, followed by partial melting during which the degree of melting of the metasomatized mantle source increased linearly with the amount of subduction component added to the mantle source. The calc-alkaline magmas may have formed by remelting of a highly depleted source, which became enriched in some trace elements derived from the source of the subsequent alkaline magmatism. The geology and geochemistry of the Karmøy Ophiolite Complex suggest growth of an island-arc upon newly-formed oceanic crust, followed by arc-splitting and the development of a new basin.     

中国东部新生代玄武岩的地球化学──Ⅰ．主元素和微量元素组成：岩石成因及源区特征

所研究的玄武岩包括拉斑玄武岩、碱性玄武岩、苦橄粗玄岩和钾质玄武岩。主元素和微量元素的组成变化表明，中国东部玄武岩既是不同深度地幔部分熔融的产物，又经历了岩浆结晶分异作用。强不相容元素比值的变化特征显然与岩石圈地幔交代作用有关。软流圈地幔的上涌并导致上覆不均一的岩石圈地幔的部分熔融是形成中国东部新生代玄武岩的主要机制。     

利用原生岩浆定量反演原岩微量元素丰度的方法

利用同源不同程度平衡部分熔融作用形成的两种原生岩浆岩的微量元素浓度，提出了一种定量反演原岩微量元素丰度的方法。反演前不需要做任何人为假设，为定量研究源区的微量元素地球化学提供了一个有力的手段。对汉诺坝新生代橄榄拉斑玄武岩和碱性玄武岩的成因及地幔源区特征作了讨论。反演结果显示本区地幔相对球粒陨石有过明显的ＲＥＥ富集过程，并且不同的ＲＥＥ富集程度存在显著的差异。     

Geochemistry of eclogites of the Tso Morari complex,Ladakh, NW Himalayas:Insights into trace element behavior during subduction and exhumation

Whole rock major and trace element compositions of seven eclogites from the Tso Morari ultra-high pressure(UHP) complex, Ladakh were determined with the aim of constraining the protolith origins of the subducted crust. The eclogites have major element compositions corresponding to sub-alkaline basalts. Trace element characteristics of the samples show enrichment in LILE's over HFSEs(Rb, Th, K except Ba) with LREE enrichments((La/Lu)n = 1.28-5.96). Absence of Eu anomaly on the Primitive Mantle normalized diagram suggests the absence of plagioclase fractionation. Positive correlation between Mg# with Ni and Cr suggests olivine fractionation of mantle melts. Narrow range of(La/Yb)n(2.1-9.4) and Ce/Yb(6.2-16.2) along with Ti/Y(435-735) ratios calculated for the Tso Morari samples is consistent with generation of melts by partial melting of a garnet free mantle source within the spinel peridotite field. Ternary diagrams(viz. Ti-Zr-Y and Nb-Zr-Y) using immobile and incompatible elements show that the samples range from depleted to enriched and span from within plate basalts(WPB)to enriched MORB(E-MORB) indicating that the eclogite protoliths originated from basaltic magmas.Primitive Mantle normalized multi element plots showing significant Th and LREE enrichment marked by negative Nb anomalies are characteristic of continental flood basalts. Positive Pb, negative Nb, high Th/Ta, a narrow range of Nb/La and the observed wide variation for Ti/Y indicate that the Tso Morari samples have undergone some level of crustal contamination. Observed geochemical characteristics of the Tso Morari samples indicate tholeiitic compositions originated from enriched MORB(E-MORB) type magmas which underwent a limited magmatic evolution through the process of fractional crystallization and probably more by crustal contamination. Observed geochemical similarities(viz. Zr, Nb, La/Yb, La/Gd,La/Nb, Th/Ta ratios and REE) between Tso Morari eclogites and the Group I Panjal Traps make the trap basalt the most likely protoliths for the Tso Morari eclogites.     

Contemporaneous Convergent Margin and Intraplate Magmatism, North Island, New Zealand

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.     

Post-collisional Tertiary–Quaternary mafic alkalic magmatism in the Carpathian–Pannonian region: a review

Mafic alkalic volcanism was widespread in the Carpathian–Pannonian region (CPR) between 11 and 0.2 Ma. It followed the Miocene continental collision of the Alcapa and Tisia blocks with the European plate, as subduction-related calc-alkaline magmatism was waning. Several groups of mafic alkalic rocks from different regions within the CPR have been distinguished on the basis of ages and/or trace-element compositions. Their trace element and Sr–Nd–Pb isotope systematics are consistent with derivation from complex mantle-source regions, which included both depleted asthenosphere and metasomatized lithosphere. The mixing of DMM-HIMU-EMII mantle components within asthenosphere-derived magmas indicates variable contamination of the shallow asthenosphere and/or thermal boundary layer of the lithosphere by a HIMU-like component prior to and following the introduction of subduction components.Various mantle sources have been identified: Lower lithospheric mantle modified by several ancient asthenospheric enrichments (source A); Young asthenospheric plumes with OIB-like trace element signatures that are either isotopically enriched (source B) or variably depleted (source C); Old upper asthenosphere heterogeneously contaminated by DM-HIMU-EMII-EMI components and slightly influenced by Miocene subduction-related enrichment (source D); Old upper asthenosphere heterogeneously contaminated by DM-HIMU-EMII components and significantly influenced by Miocene subduction-related enrichment (source E). Melt generation was initiated either by: (i) finger-like young asthenospheric plumes rising to and heating up the base of the lithosphere (below the Alcapa block), or (ii) decompressional melting of old asthenosphere upwelling to replace any lower lithosphere or heating and melting former subducted slabs (the Tisia block).     

Spatial and temporal variations in the compositions of Upper Miocene to Recent basic lavas in the northern main Ethiopian rift: Implications for the causes of Cenozoic magmatism in Ethiopia

The rate of lithospheric extension has previously been suggested as the most important factor governing the compositions of magmas generated in the Cenozoic Ethiopian volcanic province (CEVP). However, the distribution and chemistry of volcanic rocks extending from the western plateau margin at Addis Ababa to the rift floor in Nazret, northern sector of the main Ethiopian rift (MER), suggest that transitional magmatism in the region may have been triggered by an increase in the amount of lithospheric extension in the Early Pliocene. The rocks occur across an area of variable crustal thickness and show a general age progression from Upper Miocene (≤9 Ma) to Recent toward the rift. Alkalic basalts are extensive in the western part of the rift and along its margin but are found only locally within the rift, whereas transitional basalts are found within the rift only. Both types of basalts appear to have been derived from a common mantle source. In contrast, alkalic and transitional basalts on the Ethiopian plateau are mutually exclusive in terms of their spatial distribution, but exhibit a compositional contiguity which suggests that transitional magmas on the plateau formed at the expense of alkalic magmas, i.e. by equilibration of alkalic magmas at relatively shallow depth. The alkalic basalts bear clear record of a decrease in the degree of partial melting with time, suggesting that magmatism on the plateau was possibly triggered by a transient thermal anomaly.     

Geochemistry of rare high-Nb basalt lavas: Are they derived from a mantle wedge metasomatised by slab melts?

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.     

Fluorine in basalts from Iceland

The fluorine content of Icelandic tholeiitic and alkaline basalts matches values found in similar rocks from other areas. Covariation between fluorine and incompatible minor elements such as potassium or phosphorus is found in evolved tholeiites and alkali basalts. Lack of such covariation in primitive olivine tholeiites indicates that fluorine and other incompatible minor and trace elements are not controlled by minerals such as amphibole, mica or apatite in the mantle residue, and that the covariation between these elements in the evolved basalts cannot be inherited from the mantle. Model calculations on rocks from the Langjökull area show that olivine tholeiite suites are, if derived by simple fractional crystallization, enriched in incompatible elements much in excess of the increase due to crystal removal. These observations are taken to indicate that the well documented covariation between fluorine and other incompatible elements is not established until evolution of the basaltic magma has started in crustal holding chambers. The constancy of element ratios and enrichment in excess of what can be accounted for by crystal fractionation or incremental addition of new batches of primitive magmas does indicate (1) mineral control involving amphibole, mica or apatite and (2) addition of fluorine, potassium and phosphorous from an external source. It is argued that this source is the crustal envelope of the holding chamber.