Peralkaline acid tendencies in Gran Canaria (Canary Islands)

The study of a volcanic series from the island of Gran Canaria (Canary Islands) in which alkaline and peralkaline, saturated and undersaturated rocks coexist, is reported here. Materials with high volatile content (ignimbritic trachytes) were first emitted and the series ended with the eruption of phonolitic lavas. The average peralkalinity index in these rocks is typically about 1.0 and, therefore, peralkaline rocks coexist with non-peralkaline ones. However, a maximum in peralkalinity is found in the ignimbritic rocks of the lower part of the series. In spite of the evident acid peralkaline tendencies of these rocks, it does not seem appropriate to classify them as pantellerites or comendites. Nor are they consistent with the genetic processes proposed for rocks of similar composition and oceanic environment.The crystallization of the feldspars controls the variation trends among the different magmas but the fractionation alone does not sufficiently explain the genesis of successive fluids. Various factors seem to point to the important role which a gas-transfer process causing a geochemical stratification inside the magmatic chamber may have played.The occurrence of peralkaline silicics at Gran Canaria, which is located for away from the active Mid-Atlantic ridge, is not related to transitional basalts. These rocks are a deviation from the main undersaturated alkalic trend which characterizes the volcanism of the Canary Islands, their genesis being related to the realization of favourable local volcanic conditions.     

A high-pressure experimental study on the evolution of the silicic magmatism of the Main Ethiopian Rift

In this contribution we report the results of an experimental study that investigated equilibrium and fractional crystallization of hydrous, transitional alkaline basalt at low oxygen fugacity, under lower to middle crustal conditions to constrain the generation of subaluminous and peralkaline differentiation products that typically occur in rift systems. The experiments reveal that liquids produced by equilibrium crystallization in the range 0.7–1 GPa cannot cross the subaluminous/peralkaline compositional divide. In contrast, fractional crystallization experiments under isobaric and polybaric conditions approach closer the naturally observed trend from subaluminous to evolved peralkaline products suggesting that polybaric differentiation starting at elevated pressures can indeed lead to the transition from subaluminous to peralkaline derivative liquids. The presence of water in the parental magmas of silicic derivative products is of prime importance for the fractionation equilibria as well as for the mobility of such magmas toward shallow crustal levels.

We suggest that peralkaline magmas in rift environments are indicative for differentiation under relatively low oxygen fugacity conditions in an extensional environment characterized by a high degree of crustal fracturing that allows rapid upward migration of mafic parental magmas and formation of shallow magma reservoirs. Crystallization–differentiation of parental, hydrous transitional alkaline basalt in such reservoirs is controlled by low pressure phase equilibria that typically evolve through early saturation of anorthite-rich plagioclase and suppressed amphibole crystallization resulting in ‘low-alumina’, peralkaline derivative liquids.     

Peralkaline silicic melts of island arcs, active continental margins, and intraplate continental settings: Evidence from the investigation of melt inclusions in minerals and quenched glasses of rocks

Based on the analysis of data on the composition of melt inclusions in minerals and quenched glasses of igneous rocks, we considered the problems of the formation of peralkaline silicic magmas (i.e., whose agpaitic index, the molar ratio AI = (Na₂O + K₂O)/Al₂O₃, is higher than one). The mean compositions of peralkaline silicic melts are reported for island arcs and active continental margins and compared with the compositions of melts from other settings, primarily, intraplate continental areas. Peralkaline silicic rocks are rather common in the latter. Such rocks are rare in island arcs and active continental margins, but agpaitic melts were observed in inclusions in phenocrysts of plagioclase, quartz, pyroxene, and other minerals. Plagioclase fractionation from an alkali-rich melt with AI < 1 is considered as a possible mechanism for the formation of peralkaline silicic melts (Bowen’s plagioclase effect). However, the analysis of available experimental data on plagioclase-melt equilibria showed that natural peralkaline melts are almost never in equilibrium with plagioclase. For the same reason, the melting of the majority of crustal rocks, which usually contain plagioclase, does not produce peralkaline melts. The existence of peralkaline silicic melt inclusions in plagioclase phenocrysts suggests that plagioclase can crystallize from peralkaline melts, and the plagioclase effect may play a certain role. Another mechanism for the formation of peralkaline silicic magmas is the melting of alkali-rich basic and intermediate rocks, including the spilitized varieties of subalkali basalts.     

Trace-element sanidine/glass distribution coefficients for peralkaline silicic rocks and their implications to peralkaline petrogenesis

Sanidine/glass distribution coefficients for 11 trace elements have been determined on six peralkaline and two subalkaline silicic rocks. Distribution coefficients for Na, Sc, Fe, Cs, La, Ce, Sm, Tb and Lu from this study and the literature show little variation, within analytical uncertainty, for silicic rocks of peralkaline and subalkaline affinity. Distribution coefficients for Eu and Rb show a marked decrease with increasing peralkalinity. This variation may be the result of the decrease in the degree of polymerization from subalkaline to peralkaline silicic melts. Previous studies involving modelling of peralkaline rocks have selected, incorrectly, Eu and Rb sanidine/glass distribution coefficients determined from subalkaline silicic rocks.     

吉林省白头山火山岩的微量元素及其岩石学意义

白头山火山岩中含有一套粗面岩—钠碱流岩,与下伏的长白山玄武岩组成一个岩石系列。在白头山火山岩中,REE、Zn、Zr等元素十分富集,而过渡元素及Sr、Ba等元素极其贫 化。REE配分具明显的Eu负异常,许多不相容元素在岩石系列中表现出良好的线性关系。依据微量元素行为的数学模式对这些特征进行定性分析和定量模拟,其结果表明白头山火山岩是由长白山玄武岩岩浆经结晶分异形成的。     

Influence of oxygen fugacity on mineral compositions in peralkaline melts: The Katzenbuckel volcano, Southwest Germany

The igneous rocks of the Katzenbuckel, Southwest Germany, represent a unique and unusual alkaline to peralkaline association within the European Volcanic Province. The magmatic activity can be subdivided into two main phases. Phase I comprises the main rock bodies of phonolite and nepheline syenite, which were later intruded by different peralkaline dyke rocks (tinguaites and alkali feldspar syenite dykes) of phase II. The dyke assemblage was accompanied by magnetite and apatite veins and was followed by a late-stage pneumatolytic activity causing autometasomatic alterations.

As is typical for alkaline to peralkaline igneous rocks, early mafic minerals of phase I rocks comprise olivine, augite and Fe–Ti oxides, which are substituted in the course of fractionation by Na-amphibole and Na-pyroxene. For the early magmatic stage, calculated temperatures range between 880 and 780 °C with low silica activities (0.4 to 0.6) but high relative oxygen fugacities between 0.5 and 1.9 log units above the FMQ buffer. Even higher oxygen fugacities (above the HM buffer) are indicated for the autometasomatic alteration, which occurred at temperatures between 585 and 780 °C and resulted in the formation of pseudobrookite and hematite.

The unusually high oxygen fugacities (even during the early magmatic stage) are recorded by the major element compositions of the mafic minerals (forsterite content in olivine between 68 and 78 mol%, up to 6.2 wt.% ZrO₂ and 8.5 wt.% TiO₂ in clinopyroxene), the unusual mineral assemblages (pseudobrookite, freudenbergite) and by the enrichment of Fe³⁺ in the felsic minerals (up to 2.8 wt.% Fe₂O₃ in alkali feldspar and up to 2.6 wt.% Fe₂O₃ in nepheline). These observations point to a metasomatically enriched and highly oxidized lithospheric mantle as a major source for the Katzenbuckel melts.     

Trachytes,comendites, and pantellerites of the Late Paleozoic bimodal rift association of the Noen and Tost ranges,southern Mongolia: Differentiation and contamination of peralkaline salic melts

The bimodal association of the Noen and Tost ranges is ascribed to the Gobi-Tien Shan rift zone and was formed 318 Ma ago at the continental margin of the North Asian paleocontinent. It is made up of volcanic series of alternating basalts and peralkaline rhyolites with subordinate trachytes, dike belts, and massifs of peralkaline granites. The association also includes a coeval massif of biotite granites. Based on Al₂O₃ and FeO_tot contents, the peralkaline rhyolites are subdivided into comendites (FeO_tot 1.5–5.7 wt %, Al₂O₃ 10.5–15.4 wt %) and pantellerites (FeO_tot 5.2–7.5 wt %, Al₂O₃ 9.1–10.2 wt %). The peralkaline salic rocks of the bimodal association were formed by the crystallization differentiation of rift basaltic magmas combined with crustal assimilation. The comendites, pantellerites, and peralkaline granites inherited negative Nb and Ta and positive K and Pb anomalies from basalts. They are also similar to basalts in Nd isotope composition (?_Nd(T) = 5.5–7.4) and have nearly mantle oxygen isotope composition (δ¹⁸O = 5.9–7.3‰). The most differentiated and least contaminated rocks of the bimodal series of the Noen and Tost ranges are pantellerites. Calculations indicate that the fraction of the residual pantellerite melt was 8% or less of the parental basaltic magma. The comendites were derived from peralkaline salic melts by the assimilation of anatectic crustal melts compositionally similar to biotite granites. The formation of the latter within the Noen and Tost ranges is explained by the specific geodynamic position of the Gobi-Tien Shan rift zone, which was formed near a paleocontinental margin that evolved in an active margin regime shortly before the beginning of rifting.     

Structure,petrology and geochemistry of the Abu Dom alkaline ring-complex,Bayuda Desert,Sudan

The Abu Dom complex is one of a cluster of Younger Granite ring-complexes piercing the Proterozoic gneisses of the Bayuda Desert of Sudan. Intrusive rocks predominate and range from early metaluminous syenites to later peralkaline syenites and granites. They are disposed as ring-dykes, nested intrusions, and cone-sheet swarms. Field evidence and geochemical variation indicate that the peralkaline rocks evolved from a metaluminous syenitic parent magma as a result of high-level fractionation. The suite carries a clear within-plate signature exemplified by marked enrichments in HFS elements such as Zr and Nb.     

The Serra da Graciosa A-type Granites and Syenites, southern Brazil. Part 3: Magmatic evolution and post-magmatic breakdown of amphiboles of the alkaline association

Amphiboles are the main mafic minerals in most metaluminous to peralkaline alkali-feldspar granites and syenites, and they usually preserve an important record of the compositional evolution of the melts from which they crystallize. In the alkaline association of the Serra da Graciosa A-type Granites and Syenites (southern Brazil), amphibole compositions span a large range, including calcic, sodic–calcic, and sodic amphiboles. Calcic amphiboles are typically observed in the metaluminous rocks, while sodic amphiboles are characteristic of the more strongly peralkaline rocks; sodic–calcic amphiboles are found in intermediate varieties. Compositional variations record the differentiation trends within two petrographic series of the alkaline association. The overall evolution of amphibole compositions is similar in both: they reveal a progressive increase in Na and Fe³⁺ with differentiation (increase in alkalinity of the magmas), a characteristic shared by undersaturated peralkaline (or agpaitic) differentiation trends. In detail, however, the evolutions of the amphibole compositions in the two series are distinct. In Alkaline series 1, the cores of the crystals form a continuum from calcic to sodic compositions, with the exception of a small compositional gap within the sodic–calcic amphiboles. The rims, however, show compositions that diverge from this main trend; this divergence results from increasing amounts of the oxy-amphibole component, and reflects more oxidizing conditions at the final stages of magmatic crystallization. In Alkaline series 2, these oxidation trends are much more subtle and a reverse trend is observed in the sodic amphiboles. Sodic–calcic amphiboles are in several cases replaced by intergrowths of post-magmatic sodic amphibole and Al-poor (“tetrasilicic”) biotite.     

Comparison of melting relationships of some plutonic and volcanic peralkaline undersaturated rocks

From previous studies and from results of melting and crystallization sequences determined for four plutonic rocks and for four glass-bearing volcanic rocks all with peralkaline chemistry, the degree of peralkalinity, ZrO₂, TiO₂, F and Cl contents of the plutonic and holocrystalline volcanic rocks can be correlated with their melting intervals. This correlation does not hold for the glassy volcanic rocks. Analyses of whole rock and coexisting glasses suggest that rapidly chilled peralkaline volcanics may behave differently from holocrystalline peralkaline rocks due to different cooling rates causing variations in the distribution of volatiles such as Cl, between liquid and solid phases of the crystallizing melt.     

Petrology,volume and age relations of alkaline and saturated peralkaline volcanics from Terceira,Azores

Four volcanoes form Terceira, one of the islands of the Azores group; three contain both basaltic and peralkaline and one only peralkaline rocks. A recently active basaltic fissure zone trends NW-SE across the island.The rocks fall into the alkaline olivine basalt suite although some young basalts are of transitional affinity. The geochemistry shows two general basaltic series: 1) undersaturated, found in lavas of the oldest volcano and in some recent fissure zone basalts and hawaiites; 2) saturated, found in the younger basaltic lavas.Since the emergence of Terceira there has been a contemporaneity of basalt and salic peralkaline lavas. The younger rocks show a bimodal composition distribution, the most voluminous compositions being alkali olivine basalt and comendite with negligible volume in the benmoreite-trachyte range. Two processes appear viable for the derivation of voluminous oversaturated peralkaline rocks: 1) partial melting of upper mantle material giving small magma batches of contrasting composition or 2) fractionation from a transitional basaltic parental magma.Now at Department of Geology, Victoria University of Wellington, New Zealand.     

Geochemistry of intrusive rocks associated with the Latir volcanic field,New Mexico,and contrasts between evolution of plutonic and volcanic rocks

Plutonic rocks associated with the Latir volcanic field comprise three groups: 1) 25 Ma high-level resurgent plutons composed of monzogranite and silicic metaluminous and peralkaline granite, 2) 23–25 Ma syenogranite, and alkali-feldspar granite intrusions emplaced along the southern caldera margin, and 3) 19–23 Ma granodiorite and granite plutons emplaced south of the caldera. Major-element compositions of both extrusive and intrusive suites in the Latir field are broadly similar; both suites include high-SiO₂ rocks with low Ba and Sr, and high Rb, Nb, Th, and U contents. Moreover, both intermediateto siliciccomposition volcanic and plutonic rocks contain abundant accessory sphene and apatite, rich in rare-earth elements (REE), as well as phases in which REE's are essential components. Strong depletion in Y and REE contents, with increasing SiO₂ content, in the plutonic rocks indicate a major role for accessory mineral fractionation that is not observed in volcanic rocks of equivalent composition. Considerations of the rheology of granitic magma suggest that accessory-mineral fractionation may occur primarily by filter-pressing evolved magmas from crystal-rich melts. More limited accessory-mineral crystallization and fractionation during evolution of the volcanic magmas may have resulted from markedly lower diffusivities of essential trace elements than major elements. Accessory-mineral fractionation probably becomes most significant at high crystallinities. The contrast in crystallization environments postulated for the extrusive and intrusive rocks may be common to other magmatic systems; the effects are particularly pronounced in highly evolved rocks of the Latir field. High-SiO₂ peralkaline porphyry emplaced during resurgence of the Questa caldera represents non-erupted portions of the magma that produced the Amalia Tuff during caldera-forming eruption. The peralkaline porphyry continues compositional and mineralogical trends found in the tuff. Amphibole, mica, and sphene compositions suggest that the peralkaline magma evolved from metaluminous magma. Extensive feldspar fractionation occurred during evolution of the peralkaline magmas, but additional alkali and iron enrichment was likely a result of high halogen fluxes from crystallizing plutons and basaltic magmas at depth.     

Distribution of nickel,copper and zinc in the volcanic series of Erta'Ale,Ethiopia

NI, Cu and Zn were measured polarographically in 34 samples of volcanic rocks from the chain of Erta'Ale, Ethiopia. In this chain all rock types from picritic basalts to alkaline and peralkaline rhyolites can be found. The series is marked by a considerable iron enrichment in the intermediate stages. The distribution of Ni, Cu and Zn in the series emphasizes the efficiency of the crystal-field theory in accounting for the behaviour of the elements during magmatic fractionation. Nickel shows a regular variation throughout the trend. The variation of copper is similar to that of iron, but the relative rates of enrichment and depletion show that they are not necessarily associated with the same mineral phases. The behaviour of Zn is rather irregular.     

Relationships between Mafic and Peralkaline Silicic Magmatism in Continental Rift Settings: a Petrological, Geochemical and Isotopic Study of the Gedemsa Volcano, Central Ethiopian Rift

Petrological and geochemical data are reported for basalts andsilicic peralkaline rocks from the Quaternary Gedemsa volcano,northern Ethiopian rift, with the aim of discussing the petrogenesisof peralkaline magmas and the significance of the Daly Gap occurringat local and regional scales. Incompatible element vs incompatibleelement diagrams display smooth positive trends; the isotoperatios of the silicic rocks (⁸⁷Sr/⁸⁶Sr = 0·70406–0·70719;¹⁴³Nd/¹⁴⁴Nd = 0·51274–0·51279) encompassthose of the mafic rocks. These data suggest a genetic linkbetween rhyolites and basalts, but are not definitive in establishingwhether silicic rocks are related to basalts through fractionalcrystallization or partial melting. Geochemical modelling ofincompatible vs compatible elements excludes the possibilitythat peralkaline rhyolites are generated by melting of basalticrocks, and indicates a derivation by fractional crystallizationplus moderate assimilation of wall rocks (AFC) starting fromtrachytes; the latter have exceedingly low contents of compatibleelements, which precludes a derivation by basalt melting. ContinuousAFC from basalt to rhyolite, with small rates of crustal assimilation,best explains the geochemical data. This process generated azoned magma chamber whose silicic upper part acted as a densityfilter for mafic magmas and was preferentially tapped; maficmagmas, ponding at the bottom, were erupted only during post-calderastages, intensively mingled with silicic melts. The large numberof caldera depressions found in the northern Ethiopian riftand their coincidence with zones of positive gravity anomaliessuggest the occurrence of numerous magma chambers where evolutionaryprocesses generated silicic peralkaline melts starting frommafic parental magmas. This suggests that the petrological andvolcanological model proposed for Gedemsa may have regionalsignificance, thus furnishing an explanation for the large-volumeperalkaline ignimbrites in the Ethiopian rift. KEY WORDS: peralkaline rhyolites; geochemistry; Daly Gap; Gedemsa volcano; Ethiopian rift     

Strongly undersaturated Tertiary volcanic rocks from the Kangerdlugssuaq area, east Greenland

Erratic blocks from the interior of Kangerdlugssuaq fjord are described with chemical analyses and microprobe data for their constituent minerals. A strongly peralkaline phonolite, unlike any previously known from the province, shows that some magmas which precipitated alkali feldspar, nepheline and amphibole (magnesio-katophorite) differentiated along a trend towards increasing peralkalinity, although this trend is unknown in the nearby plutons. Feldspar-free nephelinite and less undersaturated limburgite are also encountered, which apparently provided a petrographic link between the strongly undersatrated ultramafic rocks recently discovered in the area and the alkali basalts of Prinsen af Wales Bjerge.

Recognition of these rock types provides further important analogies with the plume-generated triple junctions of the African Rift and affords samples approximating closely to the compositions of the more unusual magmas of the area.     

Petrology and Genesis of Hercynian Alkaline Orthogneisses from Provence, France

Major and trace element variations in an Ordovician alkalineorthogneiss (ortholeptynites) series of the Maures massif, France,suggest that the pre-metamorphic rocks were alkaline and peralkalinerhyolites derived by fractional crystallization from trachy-rhyoliticmagma. Differentiation proceeded under low oxygen fugacity conditions,with the production of high-silica comendites. By comparisonwith unaltered alkaline and peralkaline rhyolites, it is possibleto prove that the parental magma was not similar to the metatholeiitesthat are associated with the orthogneisses in the field. Norwere the metarhyolites derived from the alkaline to transitionalmetabasalts of the same age which occur elsewhere in the Mauresmassif. The orthogneisses have geochemical features typicalof alkaline and peralkaline rhyolites occurring with basaltsin continental, anorogenic, bimodal associations. This hypothesisis also supported by zircon morphology and mineral chemistry.The Maures massif was a within-plate continental volcanic province,whose crust underwent doming and thinning, but not break up,during lower Palaeozoic times.     

Alteration, HFSE mineralisation and hydrocarbon formation in peralkaline igneous systems: Insights from the Strange Lake Pluton, Canada

Two characteristics of peralkaline igneous rocks that are poorly understood are the extreme enrichment in HFSE, notably Zr, Nb, Y and REE, and the occurrence of fluid inclusions dominated by methane and higher hydrocarbons. Although much of the HFSE enrichment can be explained by magmatic processes, the common intense alteration of the parts of the peralkaline intrusions most enriched in these elements suggests that hydrothermal processes also play an important role in HFSE enrichment. Likewise, although the origin of the higher order hydrocarbons that occur as inclusions in these rocks is still debated, there is strong evidence that at least in some cases their formation involved hydrothermal processes. The issues of HFSE enrichment and hydrocarbon formation in peralkaline intrusions are examined using data from the Strange Lake pluton, a small, middle-Proterozoic intrusion of peralkaline granite in northeast Canada. This pluton contains some of the highest concentrations of Zr, REE and Y ever reported in an igneous body, and is characterised by abundant hydrocarbon-dominated fluid inclusions in rocks that have been hydrothermally altered, including those that form a potential HFSE ore zone. We show that HFSE at Strange Lake were partly concentrated to near exploitable levels as a result of their transport in a high salinity magmatic aqueous liquid, and that this fluid coexisted immiscibly with a carbonic phase which reacted with hydrogen and iron oxides generated during the associated hydrothermal alteration to produce hydrocarbons via a Fischer–Tropsch synthesis. As a result, hydrocarbons and HFSE mineralization are intimately associated. We then go on to show that hydrothermal alteration, HFSE mineralisation and hydrocarbons are also spatially associated in other peralkaline complexes, and present a model to explain this association, which we believe may be applicable to any peralkaline intrusion where HFSE enrichment was accompanied by calcium metasomatism, hematisation and hydrothermal fluorite. We also suggest that, even where these criteria are not satisfied, hydrothermally enriched HFSE and hydrocarbons will be intimately associated simply because they are products of the same initial magmatic fluid. Finally, we speculate that the association of HFSE and hydrocarbons may in some cases actually be genetic, if, as seems possible, unmixing or effervescence of a reduced carbonic fluid from the original magmatic fluid caused changes in temperature, pH, fO₂ or the activity of volatile ligands sufficient to induce the deposition of HFSE minerals.     

Feldspathoidal rocks from the Cainozoic volcanic province of Ethiopia

A review of the occurrence of feldspathoidal rocks in the Cainozoic volcanic province of Ethiopia is given. Ijolite and melanephelinite are described for the first time from this province. The close relationship between cross-rift transcurrent faults and situation of peralkaline rocks, including the feldspathoidal varieties, is emphasized. No feldspathoidal rocks are known from within the Ethopian rift system, being restricted to the interiors of the Ethiopian and Somalian plateaux.     

吉林省白头山火山岩的岩石学研究

白头山火山位于吉林省东部,主要由一套粗面岩—钠闪碱流岩组成。岩石中长石斑晶的成分表现出逐步富Or的趋势。单斜辉石早期向富Fe,而晚期表现为向富NaFe³⁺Si₂O₆的方向演化。矿物成分变化规律的研究揭示了白头山火山岩与长白山玄武岩之间的成因联系。岩石主要元素化学成分在过碱性酸性岩系统的Q—Ab—Or相图及SiO₂—Al₂O₂—Na₂O+K₂O图上的投影,表明了白头山火山岩的演化主要是受碱性长石的分离结晶所控制,但在从粗面岩到石英粗面岩的演化过程中涉及少量斜长石组分的分离结晶。用最小二乘法对白头山火山岩的成因及其演化过程进行了定量模拟。所得结果与岩相学和岩石化学的分析结果相吻合,证实了白头山火山岩是由长白山玄武岩分离结晶形成的成因假说。根据热力学计算和过碱性岩石的高温高压实验,推测岩浆形成温度分别为1074—928℃,形成压力约在2-3kb。     

Magmatic sources and geodynamics of the early Mesozoic Northern Mongolia-Western Transbaikalia rift zone

The Northern Mongolia-Western Transbaikalia rift zone is the largest Mesozoic riftogenic structure in eastern Asia and extends for a distance of more than 1200 km. The zone consists of depressions and grabens, which were formed between 233 and 188 Ma and are filled with basaltic and basalt-comendite (bimodal) volcanic associations accompanied by numerous peralkaline granite massifs. Geochemical and isotope (Sr, Nd, and Pb) studies showed that mantle and crustal sources contributed to the formation of the magmatic rocks of the rift zone. The basalts were formed from incompatible element-enriched mantle sources. Geochemical and isotope-geochemical data suggest that the peralkaline salic rocks (comendites and peralkaline grantoids) and basalts are genetically related and were formed by the fractionation of a common parental magma. In addition, the magmatic associations contain peralkaline granites and comendites whose isotope signatures indicate their formation through the crustal contamination of derivatives of basaltic melts. The rift zone has arisen during the formation of the Mongolia-Transbaikalia zoned magmatic area in a complex geodynamic setting, combining collision in the Mongolia-Okhotsk suture with a mantle plume impact. The rift zone occupies the northern periphery of the area, being controlled by the Northern Mongolia-Transbaikalia fault system, which marks the boundaries (sutures) of large terranes in the lithosphere. Asthenospheric traps beneath suture boundaries served as pathways for the penetration of a mantle plume into the upper lithosphere, thus playing an important role in the localization of the riftogenic processes.