Evolution of the crustal phosphorus reservoir.

The release of phosphorus (P) from crustal rocks during weathering plays a key role in determining the size of Earth's biosphere, yet the concentration of P in crustal rocks over time remains controversial. Here, we combine spatial, temporal, and chemical measurements of preserved rocks to reconstruct the lithological and chemical evolution of Earth's continental crust. We identify a threefold increase in average crustal P concentrations across the Neoproterozoic-Phanerozoic boundary (600 to 400 million years), showing that preferential biomass burial on shelves acted to progressively concentrate P within continental crust. Rapid compositional change was made possible by massive removal of ancient P-poor rock and deposition of young P-rich sediment during an episode of enhanced global erosion. Subsequent weathering of newly P-rich crust led to increased riverine P fluxes to the ocean. Our results suggest that global erosion coupled to sedimentary P-enrichment forged a markedly nutrient-rich crust at the dawn of the Phanerozoic.

Crystal scavenging from mush piles recorded by melt inclusions.

Olivine-hosted melt inclusions are commonly used to determine pre-eruptive storage conditions. However, this approach relies on the assumption that co-erupted olivines have a simple association with their carrier melts. We show that primitive olivine crystal cargoes and their melt inclusions display a high degree of geochemical disequilibrium with their carrier melts at Kilauea Volcano, Hawai'i. Within a given eruption, melt inclusions trapped in primitive olivine crystals exhibit compositional diversity exceeding that in erupted lava compositions since 1790 CE. This demonstrates that erupting liquids scavenge crystal cargoes from mush piles accumulating diverse melt inclusion populations over timescales of centuries or longer. Entrainment of hot primitive olivines into cooler, evolved carrier melts drives post-entrapment crystallization and sequestration of CO2 into vapour bubbles, producing spurious barometric estimates. While scavenged melt inclusion records may not be suitable for the investigation of eruption-specific processes, they record timescales of crystal storage and remobilization within magmatic mush piles.

Deep roots for mid-ocean-ridge volcanoes revealed by plagioclase-hosted melt inclusions.

The global mid-ocean ridge system is the most extensive magmatic system on our planet and is the site of 75 per cent of Earth's volcanism1. The vertical extent of mid-ocean-ridge magmatic systems has been considered to be restricted: even at the ultraslow-spreading Gakkel mid-ocean ridge under the Arctic Ocean, where the lithosphere is thickest, crystallization depths of magmas that feed eruptions are thought to be less than nine kilometres2. These depths were determined using the volatile-element contents of melt inclusions, which are small volumes of magma that become trapped within crystallizing minerals. In studies of basaltic magmatic systems, olivine is the mineral of choice for this approach2-6. However, pressures derived from olivine-hosted melt inclusions are at odds with pressures derived from basalt major-element barometers7 and geophysical measurements of lithospheric thickness8. Here we present a comparative study of olivine- and plagioclase-hosted melt inclusions from the Gakkel mid-ocean ridge. We show that the volatile contents of plagioclase-hosted melt inclusions correspond to much higher crystallization pressures (with a mean value of 270 megapascals) than olivine-hosted melt inclusions (with a mean value of 145 megapascals). The highest recorded pressure that we find equates to a depth 16.4 kilometres below the seafloor. Such higher depths are consistent with both the thickness of the Gakkel mid-ocean ridge lithosphere and with pressures reconstructed from glass compositions. In contrast to previous studies using olivine-hosted melt inclusions, our results demonstrate that mid-ocean-ridge volcanoes may have magmatic roots deep in the lithospheric mantle, at least at ultraslow-spreading ridges.

Major and Trace Element Analysis of Natural and Experimental Igneous Systems using LA-ICP-MS.

Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) enables spatially resolved quantitative measurements of major, minor and trace element abundances in igneous rocks and minerals with equal or better precision than many other in situ techniques, and more rapidly than labour-intensive wet chemistry procedures. Common applications for LA-ICP-MS in the Earth sciences centre on investigating the composition of natural and experimental geological materials, including: analysis of whole rock silicate glasses, flux-free pressed powder tablets and/or fused aliquots of materials; in situ probing of individual minerals, xenocrysts, fluid and melt inclusions, experimental run products, and siderophile-rich micronuggets; and multidimensional chemical mapping of complex (multiphase) materials.

The global pattern of trace-element distributions in ocean floor basalts.

The magmatic layers of the oceanic crust are created at constructive plate margins by partial melting of the mantle as it wells up. The chemistry of ocean floor basalts, the most accessible product of this magmatism, is studied for the insights it yields into the compositional heterogeneity of the mantle and its thermal structure. However, before eruption, parental magma compositions are modified at crustal pressures by a process that has usually been assumed to be fractional crystallization. Here we show that the global distributions of trace elements in ocean floor basalts describe a systematic pattern that cannot be explained by simple fractional crystallization alone, but is due to cycling of magma through the global ensemble of magma chambers. Variability in both major and incompatible trace-element contents about the average global pattern is due to fluctuations in the magma fluxes into and out of the chambers, and their depth, as well as to differences in the composition of the parental magmas.