ALBERT

Description: Transformation of refractory cratonic mantle into more fertile lithologies is the key to the fate of cratonic lithosphere. This process has been extensively studied in the eastern North China Craton (NCC) while that of its western part is still poorly constrained. A comprehensive study of newly-found pyroxenite xenoliths from the Langshan area, in the northwestern part of this craton is integrated with a regional synthesis of pyroxenite and peridotite xenoliths to constrain the petrogenesis of the pyroxenites and provide an overview of the processes involved in the modification of the deep lithosphere. The Langshan pyroxenites are of two types, high-Mg# [Mg2+/(Mg2++Fe2+)*100 = ∼ 90, atomic ratios] olivine-bearing websterites with high equilibration temperatures (880 ∼ 970 oC), and low-Mg# (70 ∼ 80) plagioclase-bearing websterites with low equilibration temperatures (550 ∼ 835 oC). The high-Mg# pyroxenites show trade-off abundances of olivine and orthopyroxene, highly depleted bulk Sr-Nd (ƐNd = +11.41, 87Sr/86Sr = ∼0.7034) and low clinopyroxene Sr isotopic ratios (mean 87Sr/86Sr = ∼0.703). They are considered to reflect the reaction of mantle peridotites with silica-rich silicate melts derived from the convective mantle. Their depletion in fusible components (e.g., FeO, TiO2 and Na2O) and progressive exhaustion of incompatible elements suggest melt extraction after their formation. The low-Mg# pyroxenites display layered structures, convex-upward rare earth element patterns, moderately enriched bulk Sr-Nd isotopic ratios (ƐNd = -14.20 ∼ -16.74, 87Sr/86Sr = 0.7070 ∼ 0.7078) and variable clinopyroxene Sr-isotope ratios (87Sr/86Sr = 0.706-0.711). They are interpreted to be crustal cumulates from hypersthene-normative melts generated by interaction between the asthenosphere and heterogeneous lithospheric mantle. Combined with studies on regional peridotite xenoliths, it is shown that the thinning and refertilization of the lithospheric mantle was accompanied by crustal rejuvenation and that such processes occurred ubiquitously in the northwestern part of the NCC. A geodynamic model is proposed for the evolution of the deep lithosphere, which includes long-term mass transfer through a mantle wedge into the deep crust from the Paleozoic to the Cenozoic, triggered by subduction of the Paleo-Asian ocean and the Late Mesozoic lithospheric extension of eastern Asia.

Description: The orogenic development after the continental collision between Laurussia and Gondwana, led to two contrasting associations of mantle-derived magmatic rocks on the territory of the Bohemian Massif: (i) a 340–310 Ma lamprophyre-lamproite orogenic association and (ii) a 300–275 Ma lamprophyre association of anorogenic affinity. Major types of potassic mantle-derived magmatic rocks recognised in the orogenic and anorogenic associations include: (i) calc-alkaline to alkaline lamprophyres, (ii) alkaline “orthopyroxene minettes” (and geochemically related rocks), and (iii) peralkaline lamproites. These three types significantly differ with respect to mineral, whole-rock and Sr–Nd–Pb–Li isotope composition, and spatial distribution. The calc-alkaline lamprophyres occur throughout the entire Saxo-Thuringian and Moldanubian zones, whereas the different types of malte-derived potassic rocks are spatially restricted to particular zones. Rocks of the Carboniferous lamprophyre-lamproite orogenic association are characterised by variable negative εNd(i) and variably radiogenic Sr(i), whereas the rocks of the Permian lamprophyre association of anorogenic affinity are characterised by positive εNd(i) and relatively young depleted-mantle Nd-model ages reflecting increasing input from upwelling asthenospheric mantle. The small variation in the Pb isotopic composition of post-collisional potassic mantle-derived magmatic rocks (of both the orogenic and anorogenic series) implies that the Pb budget of the mantle beneath the Bohemian Massif is dominated by the same crust-derived material, which itself may include material derived from several sources. The source rocks of “orthopyroxene minettes” are characterised by isotopically light (“eclogitic”) Li and strongly radiogenic (crustal) Sr and may have been metasomatised by high-pressure fluids along the edge of a subduction zone. In contrast, the strongly Al2O3 and CaO depleted mantle source of the lamproites is characterised by isotopically heavy Li and high SiO2 and extreme K2O contents. This mantle source may have been metasomatised predominantly by melts. The mantle source of the lamprophyres may have undergone metasomatism by both fluids and melts.

Description: The Lu–Hf isotope system and Sr–Nd–Hf–Os isotope systematics of mantle rocks are capable of unravelling the early processes in collision belts, especially in a hot subduction context where the Sm–Nd and U–Pb systems in crustal rocks are prone to resetting owing to high temperatures and interaction with melts during exhumation. To improve models of the Devonian–Carboniferous evolution of the Bohemian Massif, we investigated in detail mafic and ultramafic rocks (eclogite, pyroxenite, and peridotite) from the ultrahigh-pressure and ultrahigh-temperature Kutná Hora Crystalline Complex (KHCC: Úhrov, Bečváry, Doubrava, and Spačice localities). Petrography, multiphase solid inclusions, major and trace element compositions of rocks and minerals, and radiogenic isotopic data document contrasting sources and protoliths as well as effects of subduction-related processes for these rocks. The Úhrov peridotite has a depleted composition corresponding to the suboceanic asthenospheric mantle, whereas Bečváry and Doubrava peridotites represent lithospheric mantle that underwent melt refertilization by basaltic and SiO2-undersaturated melts, respectively. Multiphase solid inclusions enclosed in garnet from Úhrov and Bečváry peridotites represent trapped H2O ± CO2-bearing metasomatizing agents and Fe–Ti-rich melts. The KHCC eclogites either formed by high-pressure crystal accumulation from mantle-derived basaltic melts (Úhrov) or represent a fragment of mid-ocean ridge basalt-like gabbroic cumulate (Spačice) and crustal-derived material (Doubrava) both metamorphosed at high P–T conditions. The Lu–Hf age of 395 ± 23 Ma obtained for the Úhrov peridotite reflects garnet growth related to burial of the asthenospheric mantle during subduction of the oceanic slab. By contrast, Spačice and Doubrava eclogites yield younger Lu–Hf ages of ∼350 and 330 Ma, respectively, representing mixed ages as demonstrated by the strong granulite-facies overprint and trace element zoning in garnet grains. We propose a refined model for the Early Variscan evolution of the Bohemian Massif starting with the subduction of the oceanic crust (Saxothuringian ocean) and associated oceanic asthenospheric mantle (Úhrov) beneath the Teplá–Barrandian at ≥380 Ma, which was responsible for melt refertilization of the associated mantle wedge (Bečváry, Doubrava). This was followed by continental subduction (∼370–360 Ma?) accompanied by the oceanic slab break-off and incorporation of the upwelling asthenospheric mantle into the Moldanubian lithospheric mantle and subsequent coeval exhumation of mantle and crustal rocks at ∼350–330 Ma.

Description: The Changning–Menglian orogenic belt (CMOB) in the southeastern Tibetan Plateau is an important link between the Longmu Co–Shuanghu suture (LCSS) in the northern Tibetan Plateau and the Chiang Mai–Inthanon and Bentong–Raub sutures in Thailand and Peninsular Malaysia. These belts and sutures are generally regarded as containing the remnants of the oceanic crust of the Palaeo-Tethys that formed by seafloor spreading as a result of the separation of Gondwana- and Eurasia-derived blocks during the Middle Cambrian. In this paper we report the first discovery of abundant unaltered and retrograde eclogites that occur as irregular lenses and blocks in metasedimentary rocks of the CMOB, and these eclogites form an elongate and almost north–south-trending high-pressure (HP)–ultrahigh-pressure (UHP) metamorphic belt that is ∼200 km long and ∼50 km wide. The newly discovered phengite/talc/epidote–glaucophane eclogites, lawsonite–talc–phengite eclogites, dolomite/magnesite–kyanite eclogites and phengite–kyanite-bearing retrograde eclogites have enriched (E-) and normal mid-ocean ridge basalt (N-MORB)-like affinities and mainly positive as well as some negative whole-rock εNd values (–4·34 to +7·89), which suggest an enriched and depleted oceanic lithosphere source for their protoliths. Magmatic zircons separated from the epidote–glaucophane, magnesite–kyanite and (phengite–kyanite-bearing) retrograde eclogites gave protolith ages of 317–250 Ma, which fit well within the time frame of the opening of the Palaeo-Tethys during the Middle Cambrian and its closure during the Triassic. Abundant metamorphic zircons in the eclogites indicate a Triassic metamorphic event related to the subduction of the Palaeo-Tethys oceanic crust from 235 to 227 Ma. Taking into account previous isotopic age data, we now establish the periods of Early–Middle Triassic (246–227 Ma) and Late Triassic (222–209 Ma) as the ages of subduction and exhumation of the Palaeo-Tethyan oceanic crust, respectively. Thermodynamic modelling revealed that the eclogites record distinct HP–UHP peak metamorphic conditions of 23·0–25·5 kbar and 582–610 °C for the phengite–glaucophane eclogites, 24·0–25·5 kbar and 570–586 °C for the talc–glaucophane eclogites, 29·0–31·0 kbar and 675–712 °C for the dolomite–kyanite eclogites, and 30·0–32·0 kbar and 717–754 °C for the magnesite–kyanite eclogites. These P–T estimates and geochronological data indicate that the Palaeo-Tethys oceanic slab was subducted to different mantle depths from 75 km down to 95 km, forming distinct types of eclogite with a variety of peak eclogite-facies mineral assemblages. The eclogites consistently record clockwise metamorphic P–T–t paths characterized by a heating–compression prograde loop under a low geothermal gradient of 5–10 °C km–1, indicating the rapid subduction of cold oceanic crust at a rate of 4·5–6·0 km Ma–1, followed by isothermal or cooling–decompressive retrogression and exhumation at an average rate of 3·2–4·2 km Ma–1. The newly discovered eclogites of the CMOB with their signatures of ocean-crust subduction are petrologically, geochemically and geochronologically comparable with those of the LCSS, providing powerful support for the idea that a nearly 2000 km long HP–UHP eclogite belt extends from the northern Tibetan Plateau to the southeastern Tibetan Plateau, and that it represents the main boundary suture of the Palaeo-Tethyan domain. These results have far-reaching implications for the tectonic framework and complex metamorphic evolution of the Palaeo-Tethyan domain.

Description: Replacive symplectites (vermicular intergrowths of two or more minerals) are an important feature of layered igneous intrusions, recording evidence of late-stage reactions between interstitial liquid and crystals. They are common throughout the Layered Series of the 564 Ma Sept Iles layered intrusion in Quebec, Canada, and fall into three types: oxy-symplectites, ‘Type I’ symplectites, and ‘Type II’ symplectites. Oxy-symplectites are comprised of magnetite and orthopyroxene, nucleate on olivine primocrysts, and form via the reaction Olivine + O2 → Orthopyroxene + Magnetite; Type I symplectites (of which there are 3 distinct categories) are comprised of anorthitic plagioclase with pyroxene, amphibole, or olivine vermicules, grow from primocryst oxide grains, and replace primary plagioclase; and Type II symplectites (of which there are 2 distinct categories) are comprised of anorthitic plagioclase with orthopyroxene ± amphibole vermicules, grow from primocryst olivine grains, and replace primocryst plagioclase. Rare symplectites composed of biotite and plagioclase are also present. Symplectite growth occurred at 700-1030 °C with pressure constraints of 1-2 kbar. We propose that Type I symplectites, and some Type II symplectites, formed from interaction of primocrysts with residual Fe-rich liquid as a consequence of differential loss of an immiscible Si-rich liquid conjugate from the crystal mush. However, redistribution and concentration of hydrous fluids in incompletely solidified rock, or an increase in water activity of the interstitial melt, may be more plausible processes responsible for the formation of replacive symplectites comprising abundant hydrous mineral assemblages.

Description: Sheila Peacock reports on a meeting that explored the UK's contribution to seismology in the past, present and future.

Description: Jenny Collier , marine geophysicist and President of the BGA, explains why she is addicted to science.

Description: The Matachewan Large Igneous Province (LIP) is interpreted to have formed during the early stages of mantle plume-induced continental break-up in the early Proterozoic. When the Matachewan LIP is reconstructed to its original configuration with units from the Superior Craton and other formerly adjacent blocks (Karelia, Kola, Wyoming and Hearne), the dyke swarms, layered intrusions and flood basalts, emplaced over the lifetime of the province, form one of the most extensive magmatic provinces recognized in the geological record. New geochemical data allow, for the first time, the Matachewan LIP to be considered as a single, coherent entity and show that Matachewan LIP rocks share a common tholeiitic composition and trace element geochemistry, characterized by enrichment in the most incompatible elements and depletion in the less incompatible elements. This signature, ubiquitous in early Proterozoic continental magmatic rocks, may indicate that the Matachewan LIP formed through contamination of the primary magmas with lithospheric material or that the early Proterozoic mantle had a fundamentally different composition from the modern mantle. In addition to the radiating geometry of the dyke swarms, a plume origin for the Matachewan LIP is consistent with the geochemistry of some of the suites; these suites are used to constrain a source mantle potential temperature of c. 1500–1550°C. Comparison of these mantle potential temperatures with estimated temperatures for the early Proterozoic upper mantle indicates that they are consistent with a hot mantle plume source for the magmatism. Geochemical data from coeval intrusions suggest that the plume head was compositionally heterogeneous and sampled material from both depleted and enriched mantle. As has been documented with less ancient but similarly vast LIPs, the emplacement of the Matachewan LIP probably had a significant impact on the early Proterozoic global environment. Compilation of the best age estimates for various suites shows that the emplacement of the Matachewan LIP occurred synchronously with the Great Oxidation Event. We explore the potential for the eruption of this LIP and the emission of its associated volcanic gases to have been a driver of the irreversible oxygenation of the Earth.

Description: Olivine major and trace element compositions from 12 basalts from the southern Payenia volcanic province in Argentina have been analyzed by electron microprobe and laser ablation inductively coupled plasma mass spectrometry. The olivines have high Fe/Mn and low Ca/Fe and many fall at the end of the global olivine array, indicating that they were formed from a pyroxene-rich source distinct from typical mantle peridotite. The olivines with the highest Fe/Mn have higher Zn/Fe, Zn and Co and lower Co/Fe than the olivines with lower Fe/Mn, also suggesting contributions from a pyroxene-rich source. Together with whole-rock radiogenic isotopes and elemental concentrations, the samples indicate mixing between two mantle sources: (1) a pyroxene-rich source with EM-1 ocean island basalt type trace element and isotope characteristics; (2) a peridotitic source with more radiogenic Pb that was metasomatized by subduction-zone fluids and/or melts. The increasing contributions from the pyroxene-rich source in the southern Payenia basalts are correlated with an increasing Fe-enrichment, which caused the olivines to have lower forsterite contents at a given Ni content. Al-in-olivine crystallization temperatures measured on olivine–spinel pairs are between 1155 and 1243°C and indicate that the magmas formed at normal upper mantle (asthenospheric) temperatures of ~1350°C. The pyroxene-rich material is interpreted to have been brought up from the deeper parts of the upper mantle by vigorous asthenospheric upwelling caused by break-off of the Nazca slab south of Payenia during the Pliocene and roll-back of the subducting slab beneath Payenia. The pyroxene-rich mantle mixed with peridotitic metasomatized South Atlantic mantle in the mantle wedge beneath Payenia.

Description: To reconstruct the magmatic–hydrothermal processes leading to porphyry Mo ore formation at the Climax Mo mine, Colorado, four magma units that were emplaced before, during and shortly after the mineralization events were investigated: (1) a pre-mineralization white dike of the Alma district; (2) the syn-mineralization Chalk Mountain Rhyolite; (3) a late- to post-mineralization rhyolite porphyry dyke; (4) a mafic enclave within the productive Bartlett stock. Melt inclusions, mineral inclusions and fluid inclusions in quartz phenocrysts were investigated by means of laser ablation inductively coupled plasma mass spectrometry, electron microprobe and microthermometry. Based on melt inclusion data both the Chalk Mountain Rhyolite and the rhyolite porphyry were ~10 times more fractionated than average granite and show geochemical characteristics of topaz rhyolites. They were saturated in magnetite, Mn-rich ilmenite, fluorite, aeschynite, monazite, pyrrhotite and thorite, and crystallized predominantly at 710–730°C, 1·2–2·6 kbar and log f O 2 FMQ + 2·2 (where FMQ is fayalite–magnetite–quartz). The silicate melt of the Chalk Mountain Rhyolite contained 3·5 ± 0·4 wt % F, 0·09 ± 0·03 wt % Cl, ≥ 3·0 wt % H 2 O, 15–90 µg g –1 Cs, 500–1500 µg g –1 Rb and 5–7 µg g –1 Mo, whereas that of the rhyolite porphyry contained 1·1 ± 0·3 wt % F and 4·9 ± 1·2 wt % H 2 O, but otherwise had a virtually identical major and trace element composition. The fluid exsolving from the latter melt had a bulk salinity of 10 ± 2 wt % NaCl equiv and contained of the order of 100 µg g –1 Mo. After emplacement of the Chalk Mountain Rhyolite magma at subvolcanic levels, extremely fractionated silicate melts coexisting with hypersaline brines (salt melts) and low-density vapor percolated at near-solidus conditions through the rock. These silicate melts contained 6·6 ± 0·4 wt % F, ≥ 7·5 ± 0·6 wt % H 2 O, 0·51 ± 0·05 wt % Cl, and up to 0·5 wt % Cs and 100 µg g –1 Mo, whereas the hypersaline brines contained 1–2 wt % Cs and 0·3–0·6 wt % Mo. However, owing to their negligible masses these liquids are unlikely to have played a major role in the mineralization process. The majority of Mo in the Climax deposit appears to have been derived from melts containing 5–7 µg g –1 Mo and bulk fluids containing ~100 µg g –1 Mo. These concentrations are similar to those found in similarly fractionated melts and fluids in barren and sub-economically mineralized intrusions. However, whereas in the latter intrusions fractionated melts occurred in a rather dispersed state, they seem to have been present as large, coherent masses in the apical parts of Climax-type porphyry Mo-forming magma systems. Efficient segregation of fractionated melts and fluids into the top of mineralizing magma chambers appears to have been promoted by high fluorine concentrations in the silicate melt, which was partly a primary feature, and partly an indirect consequence of other characteristics of within-plate magmatism.

Description: The Skaergaard intrusion, Greenland, is the type locality for Skaergaard-type mineralizations. Mineralization levels are perfectly concordant with igneous layering, up to 5 m thick, internally fractionated, and contain crystallized sulphide droplets and precious metal alloys, sulphides, arsenides and telluride. Immiscible Cu-rich sulphide droplets, formed in a mush zone below the roof, scavenged precious metals. They were subsequently dissolved and transported to the floor in late-formed, immiscible, Fe-rich mush melts. Mineralized stratigraphic intervals of floor gabbro formed in ‘proto-macrolayers‘, owing to local sulphide saturation in melt concentrated between floating plagioclase and sinking clinopyroxene. The floor mineralization is divided into four stratigraphic sections. Formation of the Lower Platinum Group Element Mineralization (LPGEM) involved: (1) crystallization of the bulk liquid liquidus paragenesis and in situ fractionation; (2) sulphide saturation and formation of sulphide droplets in melt in the upper part of ‘proto-macrolayers‘. After further in situ fractionation, the following steps occurred: (3) the onset of silicate–silicate immiscibility and the consequent loss of buoyant and immiscible Si-rich melt; (4) dissolution of unprotected droplets of sulphide melt present in the Fe-rich mush melt; (5) compaction-driven upwards loss of residual mush melt enriched in, for example, Au. The LPGEM preserves upward increasing bulk Pd/Pt (~6–13) owing to a continued supply of PGE and Au, with high Pd/Pt. The further development of the LPGEM ceased as the supply of precious metals to the floor waned. The Upper PGE Mineralization (UPGEM) subsequently formed from precious metals recycled in the floor. The UPGEM is characterized by increasing Au substitution in PGE phases, and a decrease in total PGE and Pd/Pt owing to upward fractionation in migrating mush melts and exhaustion of Pd and Pt. An upper Au-rich mineralization level (UAuM) was caused by late remobilization of Au and deposition on grain boundaries in fully crystallized gabbro. Cu concentrations (~150 ppm) are not correlated with PGE and Au. Repeated Cu mineralization levels (CuM), attaining 〉1000 ppm, occur above the Au levels, caused by local mush layer sulphide saturation. PGE, Au and Cu distributions in the floor mineralization reflect sub-liquidus, but supra-solidus, processes and reactions in mushes at the roof, wall and floor. Constraints provided by a new model for the mineralization provide the basis for re-evaluation of the solidification processes in the Skaergaard intrusion. We have identified the importance of extensive in situ fractionation and intrusion-wide elemental redistributions in immiscible Fe- and Si-rich silicate melts. Our model characterizes the floor cumulates as bulk liquid orthocumulates containing an upwards-increasing proportion crystallized from Fe-rich, immiscible mush melt. The roof-rocks are complementary to the floor, with downwards increasing proportions crystallized from the conjugate Si-rich melt. Petrographic observations and the relative timing of crystallization support the hypothesis that crystallization was restricted to marginal mush zones. Bulk melt remaining in the magma chamber evolved not, as generally assumed, as a result of loss of crystals grown from the bulk melt, but as the consequence of mixing with recycled and evolved melt expelled from the mush by compaction. Redistribution of Fe in immiscible melts may be common to mafic intrusions and puts into question the validity of petrogenetic modelling of bulk liquids in mafic intrusions based only on consideration of floor cumulates.

Description: We have determined experimentally the hydrous phase relations and trace element partitioning behaviour of ocean floor basalt protoliths at pressures and temperatures (3 GPa, 750–1000°C) relevant to melting in subduction zones. To avoid potential complexities associated with trace element doping of starting materials we have used natural, pristine mid-ocean ridge basalt (MORB from Kolbeinsey Ridge) and altered oceanic crust (AOC from Deep Sea Drilling Project leg 46, ~20°N Atlantic). Approximately 15 wt % water was added to starting materials to simulate fluid fluxing from dehydrating serpentinite underlying the oceanic crust. The vapour-saturated solidus is sensitive to basalt K 2 O content, decreasing from 825 ± 25°C in MORB (~0·04 wt % K 2 O) to 750°C in AOC (~0·25 wt % K 2 O). Textural evidence indicates that near-solidus fluids are sub-critical in nature. The residual solid assemblage in both MORB and AOC experiments is dominated by garnet and clinopyroxene, with accessory kyanite, epidote, Fe–Ti oxide and rutile (plus quartz–coesite, phengite and apatite below the solidus). Trace element analyses of quenched silica-rich melts show a strong temperature dependence of key trace elements. In contrast to the trace element-doped starting materials of previous studies, we do not observe residual allanite. Instead, abundant residual epidote provides the host for thorium and light rare earth elements (LREE), preventing LREE from being released (LREE 〈3 ppm at 750–900°C). Elevated Ba/Th ratios, characteristic of many arc basalts, are found to be generated within a narrow temperature field above the breakdown temperature of phengite, but below exhaustion of epidote. Melts with Ba/Th 〉1500 and La/Sm PUM (where PUM indicates primitive upper mantle) ~1, most closely matching the geochemical signal of arc lavas worldwide, were generated from AOC at 800–850°C.

Description: We constrain the physical nature of the magma reservoir and the mechanisms of rhyolite generation at Yellowstone caldera via detailed characterization of zircon and sanidine crystals hosted in three rhyolites erupted during the ( c . 170–70 ka) Central Plateau Member eruptive episode—the most recent post-caldera magmatism at Yellowstone. We present 238 U– 230 Th crystallization ages and trace-element compositions of the interiors and surfaces (i.e. unpolished rims) of single zircon crystals from each rhyolite. We compare these zircon data with 238 U– 230 Th crystallization ages of bulk sanidine separates coupled with chemical and isotopic data from single sanidine crystals. Zircon age and trace-element data demonstrate that the magma reservoir that sourced the Central Plateau Member rhyolites was long-lived (150–250 kyr) and genetically related to the preceding episode of magmatism, which occurred c . 256 ka. The interiors of most zircons in each rhyolite were inherited from unerupted material related to older stages of Central Plateau Member magmatism or the preceding late Upper Basin Member magmatism (i.e. are antecrysts). Conversely, most zircon surfaces crystallized near the time of eruption from their host liquids (i.e. are autocrystic). The repeated recycling of zircon interiors from older stages of magmatism demonstrates that sequentially erupted Central Plateau Member rhyolites are genetically related. Sanidine separates from each rhyolite yield 238 U– 230 Th crystallization ages at or near the eruption age of their host magmas, coeval with the coexisting zircon surfaces, but are younger than the coexisting zircon interiors. Chemical and isotopic data from single sanidine crystals demonstrate that the sanidines in each rhyolite are in equilibrium with their host melts, which considered along with their near-eruption crystallization ages suggests that nearly all Central Plateau Member sanidines are autocrystic. The paucity of antecrystic sanidine crystals relative to antecrystic zircons requires a model in which eruptible rhyolites are generated by extracting melt and zircons from a long-lived mush of immobile crystal-rich magma. In this process the larger sanidine crystals remain trapped in the locked crystal network. The extracted melts (plus antecrystic zircon) amalgamate into a liquid-dominated (i.e. eruptible) magma body that is maintained as a physically distinct entity relative to the bulk of the long-lived crystal mush. Zircon surfaces and sanidines in each rhyolite crystallize after melt extraction and amalgamation, and their ages constrain the residence time of eruptible magmas at Yellowstone. Residence times of the large-volume rhyolites (~40–70 km 3 ) are ≤1 kyr (conservatively 〈6 kyr), which suggests that large volumes of rhyolite can be generated rapidly by extracting melt from a crystal mush. Because the lifespan of the crystal mush that sourced the Central Plateau Member rhyolites is two orders of magnitude longer than the residence time of eruptible magma bodies within the reservoir, it is apparent that the Yellowstone magma reservoir spends most of its time in a largely crystalline (i.e. uneruptible) state, similar to the present-day magma reservoir, and that eruptible magma bodies are ephemeral features.

Description: We report and interpret new geochemical and Pb–Sr–Nd isotopic data from 325 samples of shield, late-shield, postshield, and rejuvenated stage lavas from Kauai and Niihau, the two most northwesterly islands in the Hawaiian island chain. Kauai is unique in the Hawaiian chain in that it exhibits a near-continuous geochemical transition from shield to postshield to rejuvenated stage volcanism between 4·4 and 3·6 Ma and has been continuously active over ~6 Myr. From c . 5·7 to 4·3 Ma, the shield stage of both islands produced tholeiitic basalts typical of other Hawaiian shield volcanoes. The Niihau basalts are more evolved and have high Gd/Yb compared with Kauai, indicating a higher residual garnet content in the source. Both Kauai and Niihau shield basalts have Kea-like trace element ratios, but isotopic ratios are transitional between Kea- and Loa-like compositions. The geochemical similarity of the two shields indicates that mantle sources in different regions of the plume source were similar, and that the 〈2 Ma Loa and Kea trends of the southeastern Hawaiian volcanoes are not observed. More Loa-like compositions are evident in shield lavas from eastern Kauai, where the enhanced Loa composition may reflect melting of low-melting temperature plume components as the island migrates off the hotter, more Kea-like, center of the Hawaiian plume. Postshield lavas and intrusive rocks on both islands are rare: Kauai includes alkalic basalts, hawaiites and mugearites that are isotopically homogeneous and include a significant depleted mantle component compared with the shield basalts, whereas the Niihau late-shield and postshield rocks consist of highly contrasting transitional tholeiites or basanites with variable but shield-like isotopic compositions. The Niihau postshield rocks represent variable, but lower degrees of melting of the shield mantle source. Large volumes of rejuvenated stage lavas cover both islands and also form submarine cone fields, but lava compositions are different. On Kauai, rejuvenated lavas range from melilitite to alkalic basalt with trace element, Nd isotope, and Pb isotope ratios that vary as a function of Th and SiO 2 content. Low-degree (high-Th) melts are dominated by a mixed Kea–Loihi component and high-degree (low-Th) melts include more of a depleted rejuvenated component (DRC) typified by rejuvenated stage lavas and xenoliths from nearby Kaula Island. With the exception of a single basanite, the Niihau rejuvenated stage lavas are uniformly alkalic basalt, with Sr and Ba excesses combined with depleted Th and Nb abundances relative to the light rare earth elements. Rejuvenated stage alkalic basalts from both islands are dominated by contributions from the DRC, which have high Sr/Ce and 87 Sr/ 86 Sr but low 206 Pb/ 204 Pb. The Sr-rich, possibly carbonate-bearing, DRC component may be distributed patchily in the rejuvenated stage mantle source such that, where present, the degree of partial melting was enhanced compared with the degree of partial melting of the Sr-poor, mixed Kea–Loihi component. Given the lack of a hiatus between postshield and rejuvenated stages on Kauai, the rejuvenated mantle source is already able to melt at the tail end of shield stage activity and no secondary melting mechanism is required to explain the rejuvenated stage.

Description: Simon Mitton summarizes the RAS Specialist Discussion Meeting that examined from a historical perspective Hoyle's remarkable career and the impact of his science, in the first of two articles on his scientific legacy.

Description: Fred Hoyle's interest in geophysics has been largely forgotten; Helge Kragh takes another look.

Description: Assessments of the risk posed by near-Earth objects ignore the possibility of a giant comet entering the inner solar system. Bill Napier, David Asher, Mark Bailey and Duncan Steel examine the likelihood and potential consequences of the appearance of such a centaur.

Description: Toby Samuels and Natasha Nicholson report on a debate over the pros and cons of turning humans into martians.

Description: Nevil Maskelyne became the fifth Astronomer Royal 250 years ago, at a time when science and politics were intertwined. Paul Edwards maps his career.

Description: Space physicist Mike Lockwood , who was awarded the RAS Gold Medal in 2015, was inspired by his school physics teacher, JFK and Feynman.

Description: Alexander Russell , Anthony Yeates and Jonathan Eastwood review the state of the art and interesting future directions in this developing field, drawing on the RAS discussion meeting held on 12 December 2014.

Description: A new thermodynamic model is presented for calculating phase relations in peridotite, from 0·001 to 60 kbar and from 800°C to liquidus temperatures, in the system NCFMASOCr. This model system is large enough to simulate phase relations and melting of natural peridotite and basaltic liquids. Calculations in the program thermocalc illustrate mantle phase relationships and melting conditions, specifically for the peridotite composition KLB-1. The garnet–spinel transition zone intersects the solidus at 21·4–21·7 kbar, where both Fe 3+ and Cr increase spinel stability, expanding the width of the transition. Orthopyroxene is lost at the solidus at 42 kbar in KLB-1, although this pressure is very sensitive to bulk composition. Calculated oxidation states are in excellent agreement with measured log f O 2 for xenolith suites with mantle Fe 2 O 3 contents in the range 0·1–0·3 wt %. It appears that mantle oxidation state is not just a simple function of P and T , but depends on phase assemblage, and may vary in a complex way within a single assemblage. The liquid model performs well, such that calculated solidus, melt productivity and liquid compositions compare favourably with those of experimental studies, permitting its use in interpolating between, and extrapolating from, experimental P–T conditions. Experimentally challenging but geologically useful regimes can be explored, such as subsolidus samples and very low melt fractions, with application to both mantle xenoliths and the origin of basalt.

Description: The anorthositic members of the Mealy Mountains Intrusive Suite (MMIS; Labrador, Canada) are host to 0·5–5 m diameter pegmatitic, pod-like segregations, originally described as graphic granite pods. U–Pb zircon geochronology confirms that the pods are coeval with the 1650–1630 Ma emplacement age range for the MMIS, yielding ages of 1654 ± 8 to 1628 ± 3·5 Ma. Petrographic and geochemical analysis of five pods from anorthositic rocks of the MMIS reveals that the pods have a diverse compositional range from monzodiorite to granite, varying from Fe-rich and Si-poor, to Fe-poor and Si-rich compositions. Fe-rich, Si-poor pods in the MMIS and other massifs (e.g. Laramie Anorthosite Complex) tend to be hosted by olivine-bearing anorthosites, whereas Si-rich, Fe-poor pods are hosted by pyroxene-bearing anorthosites. Each pod shows a range of graphic, myrmekitic and symplectitic textures, along with distinctive mineral assemblages (e.g. apatite and zircon) and highly enriched trace-element compositions. Evolved mineral assemblages, high concentrations of Fe, Ti and P (and in some cases SiO 2 ), and 10–1000 x chondrite enrichment in light rare earth elements, U, Th and Rb indicate that many of the pods are highly fractionated. The array of textural intergrowths provides clues about the final stages of crystallization in the pods and, by extension, the anorthosites. Macroscopic quartz–K-feldspar graphic intergrowths indicate high-viscosity, fluid-bearing and significantly undercooled magmatic conditions, whereas microscopic myrmekitic (plagioclase–quartz) and symplectitic (plagioclase–orthopyroxene) intergrowths on primary grain boundaries indicate replacement of phases in the presence of reactive fluids. In assessing the nature of these pegmatitic pods based on field, petrographic and geochemical evidence, we conclude that they represent the fluid-bearing, late-stage crystallization products of a residual liquid in the massif anorthosite system. The Fe and Si compositional variations observed in these late-stage pods can be linked to a fundamental olivine–pyroxene dichotomy observed in most Proterozoic anorthosite massifs, suggesting that pulses of magma experience variable contamination (in amount and/or composition) leading to varying differentiation paths. A range of lithologies (monzonites, monzonorites, ferrodiorites and jotunites) observed in similar pod-like structures, as well as dykes and plutons, has been observed in other Proterozoic anorthosite massifs and all have, at one time or another, been interpreted as the residual liquids of anorthosite crystallization. Our observation of in situ pods with similar compositions to all of the aforementioned lithologies, and displaying textures indicative of late-stage crystallization, supports the notion that all of these associated lithologies can be interpreted as comagmatic with, but variably contaminated and isolated residual liquids of, anorthosite crystallization. However, using isotopic evidence we cannot support the notion that the far larger granitic plutons associated with Proterozoic anorthosites are also residual liquids of anorthositic magma fractionation.

Description: We report the results of experiments on two natural marine sediments with different carbonate contents (calcareous clay: CO 2 = 6·1 wt %; marl: CO 2 = 16·2 wt %) at subduction-zone conditions (3 GPa, 750–1200°C). Water (7–15 wt %) was added to the starting materials to simulate the effects of external water addition from within the subducting slab. The onset of melting is at 760°C in water-rich experiments; melt becomes abundant by 800°C. In contrast, the onset of melting in published, water-poor experiments occurs at variable temperatures with the production of significant melt fractions being restricted to more than 900°C (phengite-out). The different solidus temperatures ( T solidus ) can be ascribed to variable fluid X H2O [H 2 O/(CO 2 + H 2 O)], which, in turn, depends on bulk K 2 O, H 2 O and CO 2 . Partial melts in equilibrium with residual garnet, carbonate, quartz/coesite, epidote, rutile, kyanite, phengite, and clinopyroxene are granitic in composition, with substantial dissolved volatiles. Supersolidus runs always contain both silicate melt and solute-rich fluid, indicating that experimental conditions lie below the second critical endpoint in the granite–H 2 O–CO 2 system. Carbonatite melt coexists with silicate melt and solute-rich fluid above 1100°C in the marl. The persistence of carbonate to high temperature, in equilibrium with CO 2 -rich hydrous melts, provides a mechanism to both supply CO 2 to arc magmas and recycle carbon into the deep Earth. The trace element compositions of the experimental glasses constrain the potential contribution of calcareous sediment to arc magmas. The presence of residual epidote and carbonate confers different trace element characteristics when compared with the trace element signal of Ca-poor marine sediments (e.g. pelagic clays). Notably, epidote retains Th and light rare earth elements, such that some melts derived from calcareous sediments have elevated Ba/Th and U/Th, and low La/Sm PUM , thereby resembling fluids conventionally ascribed to altered oceanic crust. Our results emphasize the importance of residual mineralogy, rather than source lithology, in controlling the trace element characteristics of slab-derived fluids.

Description: Three crystal-poor obsidian samples (one dacite, 67 wt % SiO 2 ; two rhyolites, 73 and 75 wt % SiO 2 ), which erupted effusively from monogenetic vents, contain sparse (〈2%) plagioclase phenocrysts that span a remarkably wide and continuous range in composition (≤30 mol % An). Many, but not all, of the plagioclase crystals display diffusion-limited growth textures (e.g. swallow-tails, skeletal, vermiform). Hypotheses to explain the paradox of a wide compositional range despite a low abundance of plagioclase include (1) incorporation of xenocrysts and/or magma mingling, (2) slow crystallization of plagioclase driven by slow cooling in a magma chamber, (3) slow crystallization of plagioclase followed by a resorption (e.g. heating) event, and (4) crystallization driven by rapid degassing (i.e. loss of melt H 2 O) ± rapid cooling during ascent. To test these hypotheses, a series of phase equilibrium experiments were conducted under pure-H 2 O fluid-saturated conditions in a cold-seal pressure vessel between 30 and 300 MPa and 750 and 950°C. The results show that the plagioclase population in each obsidian sample could have grown from their respective melts, with the exception of a single calcic core (An 60–63 ) in one sample. The results additionally rule out slow cooling in a magma chamber, because this would lead to equilibrium abundances of plagioclase (≤20%), which are far higher than what is observed in the samples (〈2%). Nor can resorption (i.e. heating) explain the low abundance of plagioclase, because this would eliminate the more sodic plagioclase crystals and hence the wide compositional range of plagioclase that is observed. The most viable hypothesis is that the sparse plagioclase phenocrysts grew relatively rapidly during magma ascent to the surface; this is consistent with the results of isothermal (850°C) continuous decompression experiments (2·9, 1·0, 0·8, and 0·1 MPa h –1 ), under pure-H 2 O fluid-saturated conditions, which were performed on one of the rhyolites (MLV-36; 73 wt % SiO 2 ) and quenched at P H2O = 89, 58 and 40 MPa. The four decompression rates correspond to degassing rates of 1·6, 0·56, 0·45 and 0·06 wt % H 2 O per day. Decompressions ≥1·0 MPa( P H2O ) h –1 , initiated above the liquidus, quenched to 100% glass at all final P H2O . Decompressions at 0·8 MPa( P H2O ) h –1 , also initiated above the liquidus, led to plagioclase crystals nearly five times larger than those grown in runs decompressed at the same rate, but initiated just below the plagioclase-in curve. It is the kinetic hindrance to nucleation that permits crystal growth to be concentrated on relatively few crystals, leading to larger crystals. Plagioclase growth rates from these experiments show that the largest phenocrysts (~1 mm) in the MLV-36 obsidian could have grown in 〈42 h. A cooling rate of ~1·2°C h –1 closely matches both the increase in melt viscosity with time and the effective undercooling with time that occurs during the 0·8 MPa( P H2O ) h –1 decompression over the first 50 h. The combined results point to crystallization of sparse plagioclase driven by relatively rapid rates of degassing ± cooling during ascent to the surface of melts that were initially above their liquidus. The obsidian samples must have been efficiently segregated as nearly 100% liquids from their respective source regions at H 2 O-fluid undersaturated conditions to attain a degree of superheating upon ascent before reaching fluid saturation.

Description: The Jurassic Vestfjella dyke swarm at the volcanic rifted margin of western Dronning Maud Land represents magmatism related to the incipient Africa–Antarctica rift zone; that is, rift-assemblage magmatism of the Karoo continental flood basalt (CFB) province. Geochemical and Nd–Sr isotopic data for basaltic and picritic dyke samples indicate diverse low-Ti and high-Ti tholeiitic compositions with Nd (180 Ma) ranging from +8 to –17. Combined with previously reported data on a subcategory of ferropicritic dykes, our new data facilitate grouping of the Vestfjella dyke swarm into seven geochemically distinct types. The majority of the dykes exhibit geochemical affinity to continental lithosphere and can be correlated with two previously identified chemical types (CT) of the wall-rock CFB lavas and are accordingly referred to as the CT1 and CT3 dykes. The less abundant Low-Nb and High-Nb dykes, a relatively enriched subtype of CT3 (CT3-E) dykes, and dykes belonging to the depleted and enriched ferropicrite suites represent magma types found only as intrusions. The chemically mid-ocean ridge basalt (MORB)-like Low-Nb and the depleted ferropicrite suite dykes represent, respectively, relatively high- and low-degree partial melting of the same overall depleted mantle (DM)-affinity source in the sublithospheric mantle. In contrast, we ascribe the chemically ocean island basalt (OIB)-like High-Nb dykes and the enriched ferropicrite suite dykes to melting of enriched components in the sublithospheric mantle. Geochemical modelling suggests that the low-Ti affinity CT1 and CT3, and high-Ti affinity CT3-E magma types of Vestfjella dyke may predominantly result from mixing of DM-sourced Low-Nb type magmas with 〈10 wt % of crust- and lithospheric mantle-derived melts. U/Pb zircon dating confirms synchronous emplacement of CT1 dykes and Karoo main-stage CFBs at 182·2 ± 0·9 and 182·2 ± 0·8 Ma, whereas two 40 Ar/ 39 Ar plagioclase plateau ages of 189·2 ± 2·3 Ma (CT1) and 185·5 ± 1·8 Ma (depleted ferropicrite suite), and a mini-plateau age of 186·9 ± 2·8 Ma (CT3-E) for the Vestfjella dykes raise the question of whether the onset of rift-zone magmatism could predate the province-wide c. 179–183 Ma main stage of Karoo magmatism. Notably variable Ca/K spectra suggest that younger 40 Ar/ 39 Ar plagioclase plateau ages of 173, 170, 164, and 154 Ma are related to crystallization of secondary minerals during the late-stage tectono-magmatic development of the Antarctic rifted margin. The occurrence of rare MORB- and OIB-like magma types in Vestfjella and along the African and Antarctic rifted margins suggests melting of geochemically variable depleted and enriched sublithospheric mantle beneath the Africa–Antarctica rift zone. Our models for the Vestfjella dyke swarm indicate that the voluminous lithosphere-affinity low-Ti and high-Ti rift-assemblage tholeiites could have been derived from MORB-like parental magmas by contamination, which implies sublithospheric depleted mantle as the principal source of the CFB magmas of the Africa–Antarctica rift zone.

Description: Monazite laser ablation–split-stream inductively coupled plasma–mass spectrometry (LASS) was used to date monazite in situ in Barrovian-type micaschists of the Moravian zone in the Thaya window, Bohemian Massif. Petrography and garnet zoning combined with pseudosection modelling show that rocks from staurolite–chlorite, staurolite, kyanite and kyanite–sillimanite zones record burial in the S 1 fabric under a moderate geothermal gradient from 4–4·5 kbar and ~530–540°C to 5 kbar and 570°C, 6–7 kbar and 600–640°C, 7·5–8 kbar and 630–650°C, and 8 kbar and 650°C, respectively. In the kyanite and kyanite–sillimanite zones, garnet rim chemistry and local syntectonic replacement of garnet by sillimanite–biotite aggregates point to re-equilibration at 5·5–6 kbar and 630–650°C in the S 2 fabric. Heterogeneously developed retrograde shear zones (S 3 ) are marked by widespread chloritization, but minor chlorite is present in the studied samples. Monazite abundance and size increase with metamorphic grade from 5 µm in the staurolite–chlorite zone to 〉100 µm in the kyanite and kyanite–sillimanite zones. Irrespective of the monazite-forming reaction, this is interpreted as the onset of limited prograde monazite growth at staurolite grade, and continued prograde monazite growth after the kyanite-in reaction, compatible with conditions of about 5·5 kbar and 570°C and 7·5 kbar and 630°C from pseudosection modelling. Monazite is zoned, showing embayments and sharp boundaries between zones, with low Y in the staurolite zone, high-Y cores and low-Y rims in the kyanite zone, and high-Y cores, a low-Y mantle and a high-Y rim in the sillimanite zone. The 207 Pb-corrected 238 U/ 206 Pb ages from three samples range from 344 ± 7 to 330 ± 7 Ma, irrespective of metamorphic grade. The dates from monazite inclusions are interpreted as the ages of the staurolite- and kyanite-in reactions along the prograde path at 340 and 337 ± 7 Ma, respectively. The monazite in the matrix (and some inclusions) is interpreted as dating the prograde crystallization at (340–337) ± 7 Ma within the S 1 fabric, and then being affected by recrystallization at or down to 332 ± 7 Ma in the S 2 and S 3 fabrics. The two groups of data, for 340–337 and 332 Ma, are significantly different when only their in-run uncertainties (±1–3 Myr) are compared and indicate a 9 ± 3 Myr period of monazite (re)crystallization. A systematic increase in heavy rare earth element (HREE) content with decreasing monazite age from 344 to 335 Ma is correlated with growth on the prograde P–T path; the drop in HREE of monazite at 335–328 Ma is assigned to recrystallization. The presence of chlorite even in the least retrogressed samples witnesses limited external fluid availability on the retrograde P–T path. Migration of this fluid was probably responsible for heterogeneous fluid-assisted recrystallization and resetting of original prograde monazite, even where included in garnet, staurolite or kyanite. It is suggested that the rocks passed the chlorite-in reaction on the retrograde path at 332 ± 7 Ma. The timing of burial in the Thaya window, a deformed part of the underthrust Brunia microcontinent, was coeval with exhumation of granulites and migmatites of the Moldanubian orogenic root at c. 340 Ma.

Description: The Fanshan intrusion in the North China Craton (NCC) is concentrically zoned with syenite in the core (Unit 1), surrounded by ultramafic rocks (clinopyroxenite and biotite clinopyroxenite; Unit 2), and an outer rim of garnet-rich clinopyroxenite and orthoclase clinopyroxenite and syenite (Unit 3). The intrusive rocks are composed of variable amounts of Ca-rich augite, biotite, orthoclase, melanite, garnet, magnetite and apatite, with minor primary calcite. Monomineralic apatite rocks, nelsonite and glimmerite exclusively occur in Unit 2. Geochemically, the Fanshan rocks are highly enriched in light rare earth elements (LREE) and large ion lithophile elements (LILE), moderately depleted in high field strength elements (HFSE), and have a limited range of Sr–Nd–O isotopic compositions. The similar mineralogy, mineral compositions, and trace element characteristics of the three units suggest that all the rocks are co-magmatic. The parental magma is ultrapotassic and is akin to kamafugite. Very low-degree partial melting of metasomatized lithospheric mantle best explains the geochemistry and petrogenesis of the parental magmas of the Fanshan intrusion. We propose that the mantle source may have been metasomatized by a hydrous carbonate-bearing melt, which has imprinted the enriched Sr–Nd isotopic signature and incompatible element enrichment with conspicuous negative Nb–Ta–Zr–Hf–Ti anomalies and LREE enrichments. The mantle source enrichment may be correlated with oceanic sediment recycling during southward subduction of the Paleo-Asian oceanic plate during the Carboniferous and Permian. We propose that crystal settling and mechanical sorting combined with repeated primitive magma replenishment and mixing with previously fractionated magma is the predominant process responsible for the formation of the apatite ores.

Description: Ian Crawford , Martin Elvis and James Carpenter summarize an RAS Specialist Discussion Meeting which examined how science will benefit from the use of extraterrestrial resources.

Description: Before they could join the RAS, many women were influential members of amateur astronomical societies across the country, as Allan Chapman explains.

Description: Don Kurtz , Simon Jeffrey and Conny Aerts describe discoveries in the new era of precision asteroseismology.

Description: A&G is branching out with an online platform where RAS Fellows can write about their activities, news and events, reports Sue Bowler .

Description: COPERNICUS/ESA/PPO.LABS/NORUT/COMET-SEOM INSARAP STUDY In this issue's cover feature, Tim J Wright discusses the earthquake deformation cycle and seismic hazard in the continents – the 2015 Bullerwell Lecture.

Description: The National Astronomy Meeting is in its 25th year. Ken Pounds looks back at how it started and how it has evolved.

Description: Experimental studies of mantle petrology find that small concentrations of water and carbon dioxide have a large effect on the solidus temperature and distribution of melting in the upper mantle. However, it has remained unclear what effect small fractions of deep, volatile-rich melts have on melt transport and reactive melting in the shallow asthenosphere. Here we present theory and computations indicating that low-degree, reactive, volatile-rich melts cause channelization of magmatic flow at depths approximately corresponding to the anhydrous solidus temperature. These results are obtained with a novel method to simulate the thermochemical evolution of the upper mantle in the presence of volatiles. The method uses a thermodynamically consistent framework for reactive, disequilibrium, multi-component melting. It is coupled with a system of equations representing conservation of mass, momentum, and energy for a partially molten grain aggregate. Application of this method in two-phase, three-component upwelling-column models demonstrates that it reproduces leading-order features of hydrated and carbonated peridotite melting; in particular, it captures the production of low-degree, volatile-rich melt at depths far below the volatile-free solidus. The models predict that segregation of volatile-rich, deep melts promotes a reactive channelling instability that creates fast and chemically isolated pathways of melt extraction. Reactive channelling occurs where volatile-rich melts flux the base of the silicate melting region, enhancing dissolution of fusible components from the ambient mantle. We find this effect to be similarly expressed for models of both hydrated and carbonated mantle melting. These findings indicate that despite their small concentrations, water and carbon dioxide have an important control on the extent and style of magma genesis, as well as on the dynamics of melt transport.

Description: The Royal Astronomical Society now has two medals that honour excellent research in outreach and historical science. Fittingly in this centenary year, both are named after distinguished women, reports Sue Bowler .

Description: Steve Bush , curriculum leader for science at Sackville School in West Sussex, was awarded the 2016 RAS Patrick Moore Medal for his contribution to astronomy education. But, as he explains here, it was only chance that led him to astronomy.

Description: Richard McKim gives an overview of the rather different role of women in the early British Astronomical Association.

Description: A study of whole-rock major and trace element and Sr–Nd–Pb–Hf isotope compositions, combined with zircon U–Pb ages and Hf–O isotopes, for postcollisional intermediate volcanic rocks from the Dabie orogen, China provides constraints on the origin of andesitic magmas and insights into slab–mantle interaction in continental subduction channels. The volcanic rocks exhibit variable contents of SiO 2 (50·28–63·86 wt %), MgO (1·18–4·65 wt %), (Fe 2 O 3 ) T (3·60–8·53 wt %), Al 2 O 3 (12·92–18·95 wt %), Na 2 O (2·08–6·30 wt %) and K 2 O (0·73–5·25 wt %). They are mainly trachyandesites, with lesser amounts of basaltic trachyandesite, andesite, dacite and trachyte, characterized by subduction-like trace element distribution patterns showing enrichment of large ion lithophile elements and light rare earth elements but depletion of high field strength elements. The volcanic rocks have relatively enriched Sr–Nd–Pb–Hf isotope compositions, with high initial 87 Sr/ 86 Sr ratios of 0·7075–0·7110, highly negative Nd ( t ) values of –23·1 to –15·0, Hf ( t ) values of –29·8 to –18·3 and elevated 207 Pb/ 204 Pb and 208 Pb/ 204 Pb ratios at given 206 Pb/ 204 Pb ratios. Zircon Hf–O isotope analyses yield negative Hf ( t ) values of –31·0 to –17·8 and 18 O values of 4·4–6·8 for syn-magmatic domains. Zircon U–Pb dating yields consistent Early Cretaceous ages of 124 ± 3 to 130 ± 2 Ma for magma emplacement. Residual zircon cores yield Triassic, Neoproterozoic and Paleoproterozoic U–Pb ages, consistent with the ages of tectonothermal events involving ultrahigh-pressure metamorphism and protolith formation in the Dabie orogen. The zircon cores also yield a few low to negative 18 O values. An integrated interpretation of these geochemical characteristics is that the andesitic magmas were derived by partial melting of metasomatized zones in the orogenic lithospheric mantle. The metasomatites were generated by reaction of subcontinental lithospheric mantle wedge peridotite with felsic melts that originated from deeply subducted continental crust during continental collision in the Triassic. Melt–peridotite reaction in a subduction channel is therefore a key to the origin of the mantle sources of andesitic magmas in collisional orogens.

Description: The late Proterozoic Ntaka Ultramafic Complex is a body of dominantly pyroxenitic cumulate rocks containing cyclic alternations of olivine–orthopyroxene cumulates. Chemical zoning in the pyroxenes has been imaged at 25–40 µm resolution using desktop microbeam X-ray fluorescence mapping followed up with laser ablation–inductively coupled plasma mass spectrometry analysis for minor and trace elements on selected samples. Poikilitic and granular harzburgites are finely intermingled, in some cases on a centimetre scale in the same thin section. Poikilitic varieties display spectacular textures, ranging from isolated equant orthopyroxene oikocrysts within olivine-rich heteradcumulate harzburgites to rocks composed entirely of interlocking centimetre-sized anhedral orthopyroxene oikocrysts containing sharply bounded idiomorphic Cr-enriched cores. The poikilitic harzburgites are interlayered with cumulate pyroxenites in which orthopyroxene grains show a variety of zoning patterns: Cr-rich cores similar to those in the oikocrysts; sharply bounded oscillatory zoned cores; and reverse zoning with Cr-poor cores and Cr-enriched rims. A further variation is the presence of a mingled harzburgite lithology in which dunite or poikilitic harzburgite is invaded on a centimetre scale by diffuse vein networks or patches of coarse orthopyroxenite. This range of textures and lithologies attests to a more complex set of processes than implied by the standard cumulus theory model in which oikocrysts are considered to have crystallized from intercumulus liquid within a permeable crystal mush. A range of hypotheses is proposed, including infiltration metasomatism of original olivine cumulates by migrating orthopyroxene-saturated pore fluid; however, the textural relationships, whole-rock chemistry and Cr zoning within the grains can best be explained by a model in which the orthopyroxene oikocrysts form in part or whole as mechanically accumulated cumulus grains. The complexity of zoning patterns is attributed to stirring of entrained olivine and orthopyroxene crystals within a heterogeneous flowing crystal mush, where the transporting magma has a wide range of silica contents owing to poorly stirred incorporation of siliceous country-rock material. The Cr-rich orthopyroxenite component grew from Si-enriched chromite-saturated magma. Mingled lithologies developed after accumulation as a result of percolation and infiltration metasomatism by Si-enriched liquid derived by melting of xenoliths within the crystal pile. The model may be more generally applicable: dunite–harzburgite cycles, common in many layered intrusions, may reflect variable degrees of contamination rather than cycles of fractional crystallization and replenishment.

Description: New thermodynamic data for skiagite garnet (Fe 3 Fe 2 3+ Si 3 O 12 ) are derived from experimental phase-equilibrium data that extend to 10 GPa and are applied to oxybarometry of mantle peridotites using a revised six-component garnet mixing model. Skiagite is more stable by 12 kJ mol –1 than in a previous calibration of the equilibrium 2 skiagite = 4 fayalite + ferrosilite + O 2 , and this leads to calculated oxygen fugacities that are higher (more oxidized) by around 1–1·5 logfO2 units. A new calculation method and computer program incorporates four independent oxybarometers (including 2 pyrope + 2 andradite + 2 ferrosilite = 2 grossular + 4 fayalite + 3 enstatite + O 2 ) for use on natural peridotite samples to yield optimum logfO2 estimates by the method of least squares. These estimates should be more robust than those based on any single barometer and allow assessment of possible disequilibrium in assemblages. A new set of independent oxybarometers for spinel-bearing peridotites is also presented here, including a new reaction 2 magnetite + 3 enstatite = 3 fayalite + 3 forsterite + O 2 . These recalibrations combined with internally consistent PT determinations for published analyses of mantle peridotites with analysed Fe 2 O 3 data for garnets, from both cratonic (Kaapvaal, Siberia and Slave) and circumcratonic (Baikal Rift) regions, provide revised estimates of oxidation state in the lithospheric mantle. Estimates of logfO2 for spinel assemblages are more reduced than those based on earlier calibrations, whereas garnet-bearing assemblages are more oxidized. Importantly, this lessens considerably the difference between garnet and spinel oxybarometry that was observed with previous published calibrations.

Description: The Kidnappers [~1200 km 3 dense rock equivalent (DRE)] and Rocky Hill (~200 km 3 DRE) caldera-forming events in the Taupo Volcanic Zone, New Zealand, were erupted in close succession from the Mangakino volcanic centre. They have identical radiometric ages at ~1 Ma, yet erosion along the contact between the two deposits suggests that some years to decades separated the two eruptions. Field constraints and the similarities of crystal textures and compositions and glass chemistries of both eruption deposits demonstrate that they came from one overall magmatic system with a common crystal mush source. However, second-order variations in these parameters confirm that the Kidnappers and Rocky Hill deposits represent distinct events and are not the products of a single zoned magma chamber. The systematically zoned Kidnappers fall deposits provide evidence for the tapping of three discrete magma bodies, whereas the succeeding Kidnappers ignimbrite is compositionally more diverse. The transition from fall to flow deposition marks a change in the style of caldera collapse and the simultaneous evacuation of discrete but compositionally diverse melts, each of which underwent a distinct evolution and was held at slightly different P–T conditions prior to eruption. Contrasting plagioclase and orthopyroxene zonation patterns are present in pumices originating from three discrete magma bodies. Less evolved mafic melts interacted with the system, which mobilized portions of the final erupted melt through heating and volatile or chemical exchange in the mush. The two largest Kidnappers melt-dominant bodies were re-tapped in modified form, or re-established from their common mush source, prior to the Rocky Hill event. Rocky Hill pumices contain common, fluid-affected antecrystic crystal clots derived from chamber wall material. Amphibole compositions from each eruption reflect melt evolution processes and, in particular, the contemporaneous crystallization of biotite and breakdown of orthopyroxene. Plagioclase and orthopyroxene from Rocky Hill pumices share common zonation patterns with those from the two largest magma bodies in the Kidnappers. The rapid production of new melt-dominant bodies and the triggering of the Rocky Hill eruption reflect the ability of the magmatic system to rejuvenate on a geologically short timescale. The Mangakino centre did not follow a typical cycle of decreased activity after the supervolcanic Kidnappers event, instead producing a second caldera-forming eruption, within years to decades from the same system.

Description: Ambrym, a basaltic volcano in the Vanuatu Arc, has displayed variable eruptive behaviour throughout the past century, with major eruptions occurring both on the volcano flanks and at multiple vents within its caldera. These have been interspersed with periods of relative quiescence marked by extensive passive degassing at active, intra-caldera lava lakes, which experience occasional Strombolian explosions. Volcanic rocks from all vents and eruptive styles display similar isotope and incompatible trace element compositions, suggesting that all are derived from the same primary melt by fractional crystallization. Major eruptions are commonly responsible for effusion of the least evolved lavas examined (SiO 2 ~ 50 wt %; MgO ~ 5 wt %). Although all are geochemically similar, petrological differences discriminate between lavas erupted during flank and intra-caldera eruptions. Phyric basalts with homogeneous mineral compositions are common to flank eruptions, whereas crystal-rich basalts with variable mineral compositions, many not in equilibrium with their host liquid, are a feature of intra-caldera lavas. Lava lake samples are slightly more evolved than those from effusive eruptions (SiO 2 ~ 51–52 wt %; MgO ~ 4 wt %), as a result of additional crystallization during periods of relative quiescence. The diverse petrology of the intra-caldera lavas can be explained by mixing of replenishment magmas similar to those erupted from the volcano flanks with residual magma from lava lake activity. Flank eruptions exploit dykes that bypass the shallow reservoir involved with lava lake activity, limiting their interaction with this component.

Description: The generation and evolution of basaltic magmas at Usu volcano, located at the junction between the NE Japan arc and the Kuril arc, have been investigated. The mafic products, which form the somma edifice of the volcano, consist of basalt (49·6–51·3 wt % SiO 2 ) and basaltic andesite (52·0–54·9 wt % SiO 2 ) lavas. The basaltic lavas show relatively tight compositional trends, and 87 Sr/ 86 Sr ratios tend to decrease with increasing whole-rock SiO 2 content. The water content of the basaltic magmas was determined to be ~4·8 wt % based on plagioclase–melt thermodynamic equilibrium. Using this information and an olivine maximum fractionation model, the water content of the primary Usu magma was estimated to be 3·9 wt %. Multi-component thermodynamic calculations suggest that the primary magma was generated by ~23% melting of the source mantle with ~0·94 wt % H 2 O at ~1300°C and ~1·4 GPa. The 0·94 wt % water content of the source mantle is significantly higher than that beneath volcanoes in the main NE Japan arc (generally 〈0·7 wt % H 2 O); this implies that the wedge mantle at the arc–arc junction is intensively hydrated. The temperature of the wedge mantle of ~1300°C at ~1·4 GPa is also significantly higher than that of the mantle in the main NE Japan arc. Unlike the basaltic lavas, the whole-rock compositions of the basaltic andesite lavas are scattered in Harker variation diagrams. This observation suggests that the compositional diversity was produced by at least two independent processes. To elucidate the processes responsible for this compositional diversity, principal component analysis was applied to the major element compositions of the samples. This suggests that 47% of the diversity of the whole-rock compositions can be explained by mixing with partial melts of lower crustal materials, 25% is explained by redistribution of plagioclase phenocrysts, and 16% is explained by fractionation of accessory minerals.

Description: Numerous models have been developed to simulate the reaction of magmas to changes of thermodynamic variables, such as pressure, temperature, oxygen fugacity, and water activity. However, the extensive experimental database still lacks information on the distinct effect of small amounts of H 2 O on olivine + plagioclase + clinopyroxene cotectic crystallization in tholeiitic basalt. We present an experimental study addressing the effects of pressure (at 100, 200, 400, and 700 MPa) and small amounts of H 2 O on phase relations and liquid lines of descent in three tholeiitic basalts representing different evolutionary stages of the Shatsky Rise oceanic plateau magmatic system (compositions AH6, AH3, and AH5 with 8·6, 8·0, and 6·4 wt % MgO, respectively). Two experimental approaches (dry and low H 2 O) are designed to maintain contrasting H 2 O activities during crystallization using (1) graphite–platinum double capsules to perform nearly anhydrous experiments (〈0·15 wt % H 2 O in the melt) and (2) Fe pre-saturated Au 20 Pd 80 capsules to obtain low melt H 2 O contents ranging from 0·4 to 1·1 wt % H 2 O. Under dry conditions, at lower pressures (≤400 MPa), the crystallization in the MgO-rich AH6 and intermediate AH3 basalts follows the typical sequence of tholeiitic differentiation with olivine crystallization at the liquidus followed by olivine + plagioclase and olivine + plagioclase + clinopyroxene. Both basalts are close to multiple saturation at pressures between 400 and 700 MPa. At high pressure (700 MPa) the crystallization sequence is reversed, starting with clinopyroxene at the liquidus. Under low-H 2 O conditions, AH6 and AH3 are very close to multiple saturation, even at the low pressures of 100 and 200 MPa, and the reversed crystallization sequence (clinopyroxene, plagioclase + clinopyroxene, olivine + plagioclase + clinopyroxene) is observed already at 400 MPa. In contrast to the two more MgO-rich basalts, in the most evolved AH5 basalt, clinopyroxene is the liquidus phase at all investigated pressures and under both dry and low-H 2 O conditions, followed by crystallization of plagioclase + clinopyroxene and olivine + plagioclase + clinopyroxene. The most striking observation in our experiments is that the stability of clinopyroxene increases not only with pressure increase but also in the presence of small amounts of H 2 O (when compared with dry counterparts at similar pressures). Small amounts of H 2 O increase the proportion of clinopyroxene in the olivine + plagioclase + clinopyroxene phase assemblage. Our experiments clearly show that the effect of adding 0·4 wt % H 2 O to cotectic melt compositions (e.g. CaO/Al 2 O 3 ratio at a given MgO) is similar to that caused by an increase of pressure from 100 to ~ 300 MPa. This implies that small amounts of H 2 O can lead to significant overestimation of cotectic crystallization pressures (by up to 300 MPa) and that H 2 O contents need to be taken into account in geobarometric models. Our new experiments emphasize the role of low melt H 2 O contents in stabilizing clinopyroxene and provide some new insights into the problem of the ‘pyroxene paradox’. The apparent mantle pressures obtained for some mid-ocean ridge basalts using ‘dry’ geobarometric approaches can actually represent depths within the lower crust, if small amounts of H 2 O are present. The application of our experimental data to natural Shatsky Rise basalts implies that the magmas record partial crystallization processes occurring mainly at low pressure (100 MPa), corresponding to depths of ~3 km beneath the former spreading center, although the more primitive lavas show evidence of differentiation in a deeper reservoir at ~14 km depth (400 MPa).

Description: Mantle-derived xenoliths hosted by melilitite lavas from In Teria (Ahaggar, SE Algeria) include garnet and spinel peridotites, pyroxenite and phlogopite megacrysts. The spinel and garnet peridotites record an early deformation event, which formed porphyroclastic microstructures and olivine crystal preferred orientations, followed by static infiltration of hydrous alkaline melts. This metasomatic stage (stage 1) is characterized by the crystallization of phlogopite in the garnet and spinel peridotites, amphibole in the spinel peridotites and clinopyroxene in the garnet peridotite, which record chemical equilibration with an alkaline silicate melt. These early events were largely overprinted by carbonatitic metasomatism (stage 2), which is observed only in the spinel peridotites. Spinel peridotite major and trace element compositions, as well as the compositions of newly formed minerals, are characteristic of interaction with carbonate melt, associated with strong enrichment in incompatible trace elements in clinopyroxene. This second stage was followed by crystallization of pyroxenites (stage 3) in vein conduits, probably segregated from alkaline melts. We propose a scenario in which the different metasomatic imprints record successive stages of interaction between lithospheric mantle and sublithospheric melts throughout the Cenozoic. In Sr–Nd isotope space, the host melilitites and several xenoliths are clustered and plot close to the HIMU mantle end-member. However, some peridotite xenoliths are shifted towards more radiogenic 87 Sr/ 86 Sr values. In 207 Pb/ 204 Pb– 206 Pb/ 204 Pb and 208 Pb/ 204 Pb– 06 Pb/ 204 Pb space the In Teria samples define a relatively large domain characterized by high 206 Pb/ 204 Pb and 208 Pb/ 204 Pb, consistent with a contribution of an HIMU component, considered to represent a sublithospheric signature. The highest 87 Sr/ 86 Sr values are comparable with those ascribed to the EM1 mantle end-member, representing the signature of the lower continental lithosphere, and are probably inherited from the pre-metasomatic lithospheric mantle beneath In Teria. Numerical modelling of porous percolation of melt of sublithospheric origin through an EM1-like lithospheric mantle protolith reproduces the In Teria peridotite compositions, using moderately sub-chondritic Sr/Nd values for the peridotite (e.g. In Teria garnet peridotite) and moderately super-chondritic Sr/Nd values in the melt (approximately ocean island basalt values). A few spinel peridotites require a component characterized by a 143 Nd/ 144 Nd signature higher than both the EM1 end-member and the local Ahaggar basalts; the 208 Pb/ 204 Pb compositions of several samples point to a component with a depleted mid-ocean ridge basalt (MORB) mantle (DMM) signature. Thus the lithospheric mantle beneath In Teria probably did not have a uniform EM1 signature before the onset of metasomatism; it included a DMM peridotite component as well as some peridotites with elevated 143 Nd/ 144 Nd values recording long-term LREE depletion.

Description: Modelled primary magma compositions of Palaeogene basalts from the North Atlantic Igneous Province (NAIP) require melting at mantle potential temperatures ( T P ) in the range 1480–1550°C. Modern lavas from Icelandic rift zones require T P ~ 1500°C and those from the rift flanks T P ~ 1450°C. Secular cooling of the NAIP thermal anomaly was therefore of the order of ~50°C over the past 61 Myr. There were systematic variations in T P of 50–100°C from the centre of the thermal anomaly to its margins at any one time, although limits on the stratigraphical distribution of T P determinations do not rule out thermal pulsing on a timescale of millions of years. Variation in extent of melting at similar T P was controlled by local variability in lithospheric thickness. In the west of the NAIP, lithosphere thickness varied from ~90 km at Disko Island to ~65 km at Baffin Island, with similar thickness variations being evident for magmatism in the Faroe Islands, Faroe–Shetland Basin and the British Palaeogene Igneous Province (BPIP). Mean pressure of melting was greater than or equal to the final pressure of melting; the two values converge for melting columns with a melting interval of 〈1·5 GPa, regardless of T P . The majority of the BPIP magmas were generated in the garnet–spinel transition in the upper mantle. Calculated and observed rare earth element distributions in NAIP lavas are entirely consistent with the melting regimes derived from major element melting models. This allows a calibration of rare earth element fractionation and melting conditions that can be applied to other flood basalt provinces.

Description: In the lives of the first RAS Fellows, Sue Bowler finds a snapshot of women's activities in astronomy in 1916.

Description: The dihedral angle formed at junctions between two plagioclase grains and a grain of augite is only very rarely in textural equilibrium in gabbros from kilometre-scale crustal layered intrusions. The median of a population of these disequilibrium angles, cpp , varies systematically within a single layered intrusion, remaining constant over large stretches of stratigraphy with significant increases and decreases associated with the addition or reduction respectively of the number of phases on the liquidus of the bulk magma. The stepwise changes in cpp are present in the Upper Zone of the Bushveld Complex, the Megacyclic Unit I of the Sept Iles Intrusion, and the Layered Series of the Skaergaard intrusion. The plagioclase-bearing cumulates of Rum have a bimodal distribution of cpp , dependent on whether the cumulus assemblage includes clinopyroxene. The presence of the stepwise changes is independent of the order of arrival of cumulus phases and of the composition of either the cumulus phases or the inferred composition of the interstitial liquid. The only parameter that behaves in an exactly analogous manner to cpp is the rate of change in enthalpy with temperature ( H / T ) during crystallization. Both H / T and cpp increase with the addition of a liquidus phase, and decrease with the removal of a liquidus phase. The replacement of one phase by another has little effect on H / T and no discernible effect on cpp . An increase of H / T results in an increase in the fraction of the total enthalpy budget that is the latent heat of crystallization (the fractional latent heat). It also increases the mass crystallized in each incremental temperature drop (the crystal productivity). These increases of both fractional latent heat and crystal productivity are likely to cause an increase in the time taken to form three-grain junctions in the mush via thermal buffering of a thickened mushy layer. We suggest these are the underlying causes of stepwise increases in cpp . Stepwise changes in the geometry of three-grain junctions in fully solidified gabbros thus provide a clear microstructural marker for the progress of fractionation down the liquid line of descent in layered intrusions.

Description: High-resolution sampling in monogenetic fields has the potential to reveal fine-scale heterogeneity of the mantle, a feature that may be overwhelmed by larger fluxes of magma, or missed by under-sampling. The Quaternary Auckland Volcanic Field (AVF) in northern New Zealand is a basaltic field of 51 small-volume volcanic centres, and is one of the best-sampled examples of a monogenetic volcanic field. We present data for 12 centres in the volcanic field. These show the large compositional variations between volcanoes as well as through single eruptive sequences. Whole-rock compositions range from subalkaline basalt in the larger centres, through alkali basalt to nephelinite in the smallest centres. Fractional crystallization has had a limited effect in many of the centres, but high-pressure clinopyroxene crystallization may have occurred in others. Three end-members are observed in Pb isotope space, indicating that distinct mantle source components are involved in the petrogenesis of the magmas. Whole-rock multi-element patterns show that the larger centres have prominent positive Sr anomalies and lack K anomalies, whereas the smaller centres have prominent negative K anomalies and lack Sr anomalies. The melting parameters and compositions of the sources involved are modelled using trace element ratios and multi-element patterns, and three components are characterized: (1) fertile peridotite with a Pb-isotope composition similar to Pacific mid-ocean ridge basalt; (2) eclogite domains with a HIMU-like isotope composition dispersed within the fertile peridotite; (3) slightly depleted subduction-metasomatized peridotitic lithospheric mantle (containing c . 3% subduction fluids). Modelling shows that melting in the AVF begins in garnet-bearing fertile asthenosphere (with preferential melting of eclogite domains) and that melts are variably diluted by melts of the lithospheric source. The U–Th isotope compositions of the end-members in the AVF show 230 Th excess [( 230 Th/ 232 Th) ratios of 1·11–1·38], with the samples of lower ( 230 Th/ 232 Th) exhibiting higher ( 238 U/ 232 Th), which we attribute to the dilution effect of the melts from the lithospheric mantle source. Modelling reveals a correlation between melting in the asthenosphere, the degree of melting and incorporation of the metasomatized lithospheric mantle source, and the resultant size of the volcanic centre. This suggests that the scale of the eruption may essentially be controlled by asthenospheric mantle dynamics.

Description: The origin of mafic and ultramafic sills exhibiting different whole-rock compositional profiles (e.g. I-, C-, D-, M- and S-shaped profiles) remains controversial. We have addressed this issue by revisiting three ~100 m thick Siberian dolerite sills (Vavukansky, Kuz’movsky and Vilyuysky) that display remarkable internal differentiation. The Vavukansky sill has an M-shaped profile with prominent basal and top reversals showing inward increases in whole-rock MgO, Mg-number [100Mg/(Mg + Fe)] and normative An content [100An/(An + Ab)], followed by the Layered and Upper Border Series with inward decreases in these indices. The Kuz’movsky and Vilyuysky sills both show S-shaped profiles similar to the Vavukansky sill, but lack a top reversal. These whole-rock M- and S-shaped profiles are accompanied by similar profiles in mineral compositions. Plagioclase and, to a lesser extent, olivine show systematic inward increases in An content and Mg-number, respectively, across basal and top reversals. These compositional trends are followed by inward decreases in these ratios in the interiors of the Vavukansky and Kuz’movsky sills. Currently accepted models attribute whole-rock M- and S-shaped compositional profiles to crystal settling, compositional convection or compaction operating in closed systems. Our observations challenge these traditional interpretations because variations in mineral compositions observed in marginal reversals cannot result from closed-system fractionation. We suggest instead that initially the sills evolved as open systems that were slowly inflated by magmas that became gradually more primitive with time. The inflation was accompanied by in situ crystallization that preserved the preceding fractionation history of the injected magmas by forming basal and top reversals with minerals becoming more primitive inwards. This process culminated with rapid inflation of the sills to their current size owing to a major influx of primitive magma. Subsequently, magma flow through the sills ceased and they evolved as closed systems by fractional crystallization. This resulted in the Layered and Upper Border Series with minerals becoming more evolved inwards. This model can be extended to explain other compositional profiles and petrological features in mafic and ultramafic sills.

Description: Magma dynamics and time scales during the VEI 5, 2000 bp eruption of El Misti volcano, southern Peru (EM2000BP) are investigated to address cyclic explosive activity at this hazardous volcano. The 1·4 km 3 of pumice falls and flows have abundant mingled pumice of high-K, calc-alkaline rhyolite and andesite composition. Phenocryst zoning and compositions reveal mutual exchange of plagioclase between the two magmas; amphibole in the rhyolite was derived from the andesite. Amphiboles in the andesite are predominantly unrimmed crystals whereas those in the rhyolite mostly exhibit reaction rims. Phase equilibria indicate that the andesite formed at ~900–950°C and 2–3 kbar pressure and was water-saturated with 5·1–6·0 wt % H 2 O, broadly similar to El Misti magmas overall. Amphibole, plagioclase, Ti-magnetite, and two pyroxenes were the crystallizing phases. A separate rhyolite magma existed higher in the crust at a temperature of 816 ± 30°C and ~5% H 2 O in which only plagioclase and Fe–Ti oxides were stable. The lack of cognate amphibole in the rhyolite despite H 2 O saturation requires that it staged above the stability limit of amphibole (〈100 MPa). Exchange reactions in amphibole (dominantly pargasitic) and trace element partitioning in plagioclase indicate that both andesite and rhyolite magmas were broadly constant in temperature and H 2 O content. These constraints suggest that the initially separate rhyolite and deeper andesite magmas interacted by an initial andesite recharge event that resulted in mingling and crystal exchange. A period of 50–60 days is required for amphibole introduced into the rhyolite to develop reaction rims owing to decompression. These rims are dominated by plagioclase, a consequence of the Al-rich nature of the amphibole. The lack of reaction rims on amphibole in the andesite implicates a second, more-forceful and voluminous eruption-triggering recharge event during which andesite rose rapidly from source to surface in ≤5 days at ascent rates of at least 0·023 m s –1 . Further decompression-driven crystallization is recorded in plagioclase rims and microlite growth that may have contributed to a rapid increase in viscosity leading to explosive eruption. This VEI 5 plinian eruption shares characteristics with other explosive events at El Misti on a time scale of 2000–4000 years, suggesting periodic recharge-driven explosive activity.

Description: We report structural evidence of ductile strain localization in mantle pyroxenite from the spinel to plagioclase websterite transition in the Ronda Peridotite (southern Spain). Mapping shows that, in this domain, small-scale shear zones occurring at the base of the lithospheric section are systematically located within thin pyroxenite layers, suggesting that the pyroxenite was locally weaker than the host peridotite. Strain localization is associated with a sudden decrease of grain size and increasing volume fractions of plagioclase and amphibole as a result of a spinel to plagioclase phase transformation reaction during decompression. This reaction also fostered hydrogen extraction (‘dehydroxylation’) from clinopyroxene producing effective fluid saturation that catalyzed the synkinematic net-transfer reaction. This reaction produced fine-grained olivine and plagioclase, allowing the onset of grain-size sensitive creep and further strain localization in these pyroxenite bands. The strain localization in the pyroxenites is thus explained by their more fertile composition, which allowed earlier onset of the phase transition reactions. Geothermobarometry undertaken on compositionally zoned constituent minerals suggests that this positive feedback between reactions and deformation is associated with cooling from at least 1000°C to 700°C and decompression from 1·0 to 0·5 GPa.