The relationship between magmatism and gold mineralization has been a topic of interest in understanding the formation of ore deposits. The Baizhangzi gold deposit, located in the northern margin of the North China Craton, is hosted by the Baizhangzi granite (BZG) and provides a case to evaluate the relation between granite and gold mineralization in Late Triassic. In this study, we present petrography, bulk geochemistry, zircon U-Pb isotope and trace elements data, as well as major elements of biotite and plagioclase for the BZG to evaluate the petrogenesis and link with gold mineralization. The BZG comprises biotite monzogranite, biotite-bearing monzogranite and monzogranite (BZGs). Zircon U-Pb geochronology shows that all the granitoids of BZGs were coeval with a formation age of 232 Ma. The granitoids, with high SiO2, Al2O3 and Sr, while low Y and Yb, show adakitic affinity. They are enriched in LILFs (e.g., Rb, Ba, Th, U and Sr) and LREEs, while depletion in HFSEs (e.g., Nb, Ta, P and Ti). The geochemical and mineral chemical data suggest that the granitoids have experienced the fractional crystallization of biotite + plagioclase + K- feldspar + apatite. Crystallization temperature is estimated as ca. 700°C, and pressure is between 0.71 kbar and 1.60 kbar. The monzogranite shows higher values of logfO2, △FMQ and △NNO than the biotite-bearing monzogranite, ranging from −19.76 to −11.71, −4.93 to +3.67 and −5.48 to +3.11, respectively. The fractional crystallization, together with high fO2, K-metasomatism and low evolution degree, provided favourable conditions for gold mineralization.

The Qieganbulake deposit associated with a mafic–ultramafic–carbonatite complex in the Kuluketage block is not only the world’s second-largest vermiculite deposit, but also a medium-size carbonatite-related phosphate deposit. Field observations, radiometric dating results and Sr–Nd–Hf isotopes reveal that the parental magmas of the carbonatite and mafic–ultramafic rocks are cogenetic and formed synchronously at c. 810 Ma. Geochemical characteristics and Sr–Nd–Hf–S isotopes ((87Sr/86Sr)i = 0.70581–0.70710; ϵNd(t) = −0.20 to −11.80; ϵHf(t) = −7.5 to −10.3; δ34S = +0.7 ‰ to +3.0 ‰ (some sulfides with high δ34S values (+3.2 to +6.6) were formed by late hydrothermal sulfur)), in combination with mineral compositions and previous research, strongly indicate that the Qieganbulake mafic–ultramafic–carbonatite complex formed via extensive crystal fractionation/cumulation and liquid immiscibility of a carbonated tholeiitic magma, possibly derived from partial melting of an enriched subcontinental lithospheric mantle previously modified by slab-released fluids and sediment input in a continental rift setting. The coupled enriched Sr–Nd isotopic signatures, in combination with previous research, suggest that the enriched subcontinental lithospheric mantle could have been metasomatized by asthenospheric mantle melts to different degrees. The Qieganbulake carbonatite-related phosphate ores were the products of normal fractional crystallization/cumulation of P–Fe3+ complex enriched carbonatite magma in high oxygen fugacity conditions, which was generated by liquid immiscibility of CO2–Fe–Ti–P-rich residual magma undergoing high differentiation.

The 1800 m thick preserved remnant of the Tertiary lava succession of Mull and Morvern consists of three basic mantle-derived magma types, with compositions varying from tholeiitic to mildly alkalic, and from picritic basalts to trachytes. This results in a similarly wide range in mineral compositions. Contrary to the suggestions of previous workers the mineral chemistry of the lava succession (in conjunction with published major and trace element chemistry) is strongly supportive of a fractional crystallisation origin for the more evolved lavas.

Resorped and regrown (with more basic material) plagioclase phenocrysts found in the more-evolved are indicative of magma mixing processes involving replenishment of an evolving magma chamber with more-basic magma. Lavas containing 15–20 vol.% plagioclase phenocrysts probably represent eruptions from the top of a magma chamber where flotation cumulates of plagioclase had developed. Fragmental phenocrysts found in some highly plagioclase phyric lavas (from near the top of the preserved lava succession) suggest that the eruption of lavas may have been explosive.

In this paper we present new petrological and geochemical data for two peraluminous granite batholiths (Nisa Alburquerque and Jalama batholiths) representative of the ‘Araya-type’ granites of the Central-Iberian Zone. Both granites are composite with several facies (monzogranites and leucogranites) that can be grouped into two main granite units: the external units and central units. Intrusive relationships and lack of geochemical coherence between the central and external units indicate that they are not comagmatic but represent different pulses. The central units of both batholiths are petrologically and geochemically different. On the other hand, external units show a lot of similarities and are the main object of this study. The main characteristics of the external granites can be interpreted in terms of an incomplete fractional crystallization process of early mineral phases (plg + Kf + bt) which probably took place at the level of emplacement. Other possible mechanisms of magmatic differentiation (magma mixing, restite unmixing, sequential melting) can be discarded based on field, petrography and geochemical data. We propose that the ‘Araya-type’ granites are formed by the intrusion of distinct magma pulses (central and external). Further evolution within each pulse can be due to incomplete fractional crystallization possibly taking place at the emplacement level.

Intruded into the Palaeogene lava field and underlying Moine (Neoproterozoic) crystalline basement rocks around Loch Scridain, Isle of Mull, Scotland, is a suite of high-level, inclined, xenolithic sheets, ranging in composition from basalt, through andesite and dacite, to rhyolite. These sheets, associated with the Mull central volcano, were emplaced post 55 Ma. As well as numerous crustal xenoliths, the more basic members of the complex contain a diverse suite of ultrabasic and basic xenoliths. Xenolith types include feldspathic peridotite with cumulus olivine, pyroxenite, gabbro with cumulus plagioclase and cumulus clinopyroxene, and pure anorthosite. Mineralogical data, coupled with whole-rock major- and trace-element data from a small number of the xenoliths suggest that the xenoliths represent early-formed cumulates cognate with their host basalts. Sr and Nd isotope data from the xenoliths confirms the cognate origin, and also shows that the basic magmas suffered crustal contamination at an early stage.

Magmas in Faial Island, Azores (Portugal), were mostly erupted from two fissure zones and the Caldeira central volcano during overlapping periods. The fissure zones follow extensional trends oriented WNW and ESE and erupted nepheline- to hypersthene-normative basalts and hawaiites. The Caldeira central volcano builds the central part of the island, which is cut by the fissure zones. Ne-normative basalts show similar high-field-strength element (HFSE) concentrations but higher large ion lithophile element (LILE) concentrations than hy-normative equivalents. Primitive melts were generated by small (3–5%) degrees of partial melting of garnet-bearing peridotite, variably enriched in incompatible elements. Overall, basalts from Faial show relatively higher LILE abundances and LILE/HFSE ratios than those of the other islands of the Azores and of many other volcanoes in the Atlantic area. This feature indicates the existence of chemical heterogeneities in the mantle sources characterized by variable degrees of metasomatism, both at local and regional scales. Hawaiites evolved from basalts through 30–40% fractional crystallization of mafic phases plus some plagioclase, in deep reservoirs, at about 430–425 MPa (~ 15 km). The Caldeira central volcano rocks range from basalts to trachytes. Basalts, produced under similar conditions as fissure basalts, evolved to trachytes through large degrees of polybaric fractional crystallization (100–760 MPa; i.e. ~ 3.6–26 km), involving olivine, clinopyroxene, feldspar and minor quantities of amphibole, biotite, apatite and oxides. In contrast, mafic magmas from the fissure zones were erupted directly onto the surface from magma reservoirs mainly located at the crust–mantle boundary.

A pair of samples, from host lava and an included segregation vein from the Reykjanes Peninsula, Iceland, allows the assessment of a complete fractional crystallization of an olivine tholeiite at low pressure. The final product consists of silicic glasses with bimodal composition: trondhjemitic and more rarely granitic. Compilation of data on major element compositions of Icelandic silicic rocks reveals a clear difference from those of the segregation glasses. Fractional crystallization of basalts at low pressure is therefore not the most likely mechanism for the origin of silicic magmas in Iceland. Similar conclusions have been reached in studies on O- and Th-isotope compositions. On the other hand, the trondhjemitic compositions of the glasses in the segregation vein from Reykjanes Peninsula suggest that fractional crystallization of olivine tholeiites could have played a significant role during the formation of the very early continental crust.