The composition of the Earth

This chapter reviews the present-day composition of the continental crust, the methods employed to derive these estimates, and the implications of the continental crust composition for the formation of the continents, Earth differentiation, and its geochemical inventories. We review the composition of the upper, middle, and lower continental crust. We then examine the bulk crust composition and the implications of this composition for crust generation and modification processes. Finally, we compare the Earth's crust with those of the other terrestrial planets in our solar system and speculate about what unique processes on Earth have given rise to this unusual crustal distribution.

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Composition of the Continental Crust

3.01 – Composition of the Continental Crust

The continental bio-cycling of silicon (Si) plays a key role in global Si cycle and as such partly controls global carbon (C) budget through nutrition of marine and terrestrial biota, accumulation of phytolith-occluded organic carbon (PhytOC) and weathering of silicate minerals. Despite the key role of elemental composition of phytoliths on their solubility in soils, the impact of plant cultivar and organ on the elemental composition of phytoliths in Si high-accumulator plants, such as rice (Oryza sativa) is not yet fully understood. Here we show that rice cultivar significantly impacts the elemental composition of phytoliths (Si, Al, Fe and C) in different organs of the shoot system (grains, sheath, leaf and stem). The amount of occluded OC within phytoliths is affected by contents of Si, Al and Fe in plants, while independent of the element composition of phytoliths. Our data document, for different cultivars, higher bio-available Si release from phytoliths of leaves and sheaths, which are characterized by higher enrichment with Al and Fe (i.e., lower Si/Al and Si/Fe ratios), compared to grains and stems. We indicate that phytolith solubility in soils may be controlled by rice cultivar and type of organs. Our results highlight that the role of the morphology, the hydration rate and the chemical composition in the solubility of phytoliths and the kinetic release of Si in soil solution needs to be studied further. This is central to a better understanding of the impact of soil amendment with different plant organs and cultivars on soil OC stock and on the delivery of dissolved Si as we show that sheath and leaf rice organs are both characterized by higher content of OC occluded in phytolith and higher phytolith solubility compared to grains and stems. Our study shows the importance of studying the impact of the agro-management on the evolution of sinks and sources of Si and C in soils used for Si-high accumulator plants.

/pdf/impact-of-rice-cultivar-and-organ-on-elemental-composition-4oez9nvtmp.pdf

Impact of rice cultivar and organ on elemental composition of phytoliths and the release of bio-available silicon.

[1] Estimates of the average composition of various Precambrian shields and a variety of estimates of the average composition of upper continental crust show considerable disagreement for a number of trace elements, including Ti, Nb, Ta, Cs, Cr, Ni, V, and Co. For these elements and others that are carried predominantly in terrigenous sediment, rather than in solution (and ultimately into chemical sediment), during the erosion of continents the La/element ratio is relatively uniform in clastic sediments. Since the average rare earth element (REE) pattern of terrigenous sediment is widely accepted to reflect the upper continental crust, such correlations provide robust estimates of upper crustal abundances for these trace elements directly from the sedimentary data. Suggested revisions to the upper crustal abundances of Taylor and McLennan [1985] are as follows (all in parts per million): Sc = 13.6, Ti = 4100, V = 107, Cr = 83, Co = 17, Ni = 44, Nb = 12, Cs = 4.6, Ta = 1.0, and Pb = 17. The upper crustal abundances of Rb, Zr, Ba, Hf, and Th were also directly reevaluated and K, U, and Rb indirectly evaluated (by assuming Th/U, K/U, and K/Rb ratios), and no revisions are warranted for these elements. In the models of crustal composition proposed by Taylor and McLennan [1985] the lower continental crust (75% of the entire crust) is determined by subtraction of the upper crust (25%) from a model composition for the bulk crust, and accordingly, these changes also necessitate revisions to lower crustal abundances for these elements.

https://agupubs.onlinelibrary.wiley.com/doi/epdf/10.1029/2000GC000109

Relationships between the trace element composition of sedimentary rocks and upper continental crust

The composition of the continental crust

The composition of peridotite tectonites from the Ivrea Complex, northern Italy: Residues from melt extraction

Relatively high strontium concentrations and their isotopic composition in Roman glass of the Imperial period indicate the general use of shells as carbonate raw material. Lead, iron, and barium concentrations and lead isotopes of glass of the late fourth century from Hambach and Gellep (western Germany) are conformable with the use of glass sand from Eifel rivers. Each of three pairs of six simultaneously operating Roman glasshouses in the Hambach area made its own raw glass from different quartz sands.

The Use of Marine Molluskan Shells for Roman Glass and Local Raw Glass Production in the Eifel Area (Western Germany)

Content and isotopic composition of sulphur in ultramafic xenoliths from central Asia

Analytical data on major elements and 31 trace elements in olivine nephelinites, nepheline basanites, basanitic alkali olivine basalts and their differentiates (tephrites, hawaiites, mugearites, benmoreites, latites, phonolites and trachytes) from Hegau, Kaiserstuhl, Rhon, Hessian Depression, Vogelsberg, Westerwald, Siebengebirge, E Eifel and Hocheifel are evaluated. They were based on 400 samples with new or unpublished data on about one third of the rocks. The Sr−Nd isotopic compositions for 78 rocks are included. The alkali basaltic volcanism is caused by adiabatic decompression of asthenospheric mantle updomed to a minimum depth of 50 km in connection with the Alpine continent collision. The chemical compositions of the primary basaltic melts from the different areas are similar containing about one hundred-fold enrichment of highly incompatible elements relative to the primitive mantle from partial melting of depleted and secondarily enriched peridotite. The elements Cs, K, Pb and Ti are specifically depleted in the basalts partly because of phlogopite being residual at partial melting. The Tertiary alkali basalts range in Nd-isotopic composition from 0.51288 to 0.51273 and in Sr-isotopic ratios from 0.7032 to 0.7042. These ranges indicate mixtures of HIMU, depleted and enriched mantle components in the metasomatically altered peridotite source which resembles that of certain ocean islands. The Nd-Sr-isotopic compositions of the Quaternary E Eifel are close to bulk Earth ratios. East and W Eifel plots differ distinctly from the Tertiary Hocheifel which is geographically intermediate. This isotopic difference, beside specific K/Na ratios, is probably caused by separate metasomatic pulses that immediately preceded the respective periods of volcanism. The metasomatically altered mantle had partly primitive mantle signatures (Nb/Ta, Zr/Sm and Th/U ratios) and partly ocean island (or MORB) source properties (Rb/Cs). A MORB source can be excluded because of the low K/Rb and high Th/U ratios. A correlation of δD with 87Sr/86Sr in amphibole and phlogopite and a slightly larger δ18O than in MORB is conformable with a seawater and crustal impact on the source of alkali basalts. Slightly higher than average water concentrations in the source of certain primary basaltic melts (indicated by amphibole phenocrysts in their basalts) are required for differentiation of these basalts in magma chambers of the upper crust. Model calculations are presented to explain compositions of differentiates which range from about 60% to about 20% residual melt. The latter are represented by phonolites and trachytes. The Nd- and Sr-isotopic signatures of the majority of differentiates indicate contamination by a granitic partial melt from the wall rocks of magma chambers. Olivine nephelinite magma was the common source of contaminated differentiates.

K. Hans Wedepohl

Papers

The composition of the continental crust

The composition of peridotite tectonites from the Ivrea Complex, northern Italy: Residues from melt extraction

The Use of Marine Molluskan Shells for Roman Glass and Local Raw Glass Production in the Eifel Area (Western Germany)

Content and isotopic composition of sulphur in ultramafic xenoliths from central Asia

Cenozoic alkali basaltic magmas of western Germany and their products of differentiation