Mantle Mush Compaction: a Key to Understand the Mechanisms of Concentration of Kimberlite Melts and Initiation of Swarms of Kimberlite Dykes

Kimberlite pipes or dykes tend to occur in clusters (a few kilometresin diameter) within fields 30–50 km in diameter. Theyare generally considered to originate from low degrees of partialmelting of carbonated peridotite within zones of ascending mantle.Numerical modelling shows that at the depth of formation ofkimberlite melts (>>200 km), mantle compaction processescan result in the formation of melt pockets a few tens of kilometresacross, with melt concentrations up to 7%. The initiation ofswarms of kimberlite dykes at the top of these melt pocketsis inevitable because of the large excess pressure between themelt and the surrounding solid, which exceeds the hydraulicfracturing limit of the overlying rocks. After their initiationat mantle depth the swarm of dykes may reach the surface ofthe Earth when the entire cratonic lithosphere column is inextension. We propose that kimberlite fields represent the surfaceenvelope of dyke swarms generated inside a melt pocket and thatkimberlite clusters represent the discharge of melt via dykesoriginating from sub-regions of the pocket. This model reproducesthe worldwide average diameter of kimberlite fields and is consistentwith the observation that some of the main kimberlite fieldsdisplay age ranges of c. 10 Myr. It is deduced that, at thescale of the Kaapvaal craton, different fields such as Kimberley,N. Lesotho and Orapa, dated at 80–90 Ma, probably resultfrom synchronous melt pockets forming inside an ascending mantleflow. The same model could apply to the fields of the Rietfontein,Central Cape and Gibeon districts dated at 60–70 Ma. Itis suggested that the same mantle flow that produced the Kimberley,N. Lesotho and Orapa fields migrated over 20–30 Myr afew hundred kilometres westward to form the Rietfontein, CentralCape and Gibeon fields. KEY WORDS: kimberlites; mantle; compaction; convection; volcanism     

High Field Strength Element Fractionation in the Upper Mantle: Evidence from Amphibole-Rich Composite Mantle Xenoliths from the Kerguelen Islands (Indian Ocean)

A basanite dyke in the Kerguelen Archipelago contains abundantcomposite mantle xenoliths consisting of spinel-bearing dunitescross-cut by amphibole-rich veins. Two types of veins (thickand thin) have been distinguished: the thick veins representalmost complete crystallization products of highly alkalinemelts similar to the host basanites, whereas thin veins areprecipitates from fractionates of the parental melts to thethick veins. These fractionated fluids are enriched in H₂O relativeto the parental melts. The amphiboles in the thin veins arelower in Ti and higher in Nb, Ta, Zr and Hf than amphibolesin the thick veins. This fractionation of high field strengthelements (HFSE) is consistent with a combination of the changingcomposition of the fractionated fluids and the change in intrinsicamphibole–fluid partition coefficients for HFSE in fluidswith higher a_H2O and lower a_TiO2. The trace element contentof amphiboles disseminated in dunitic wall-rocks is closelyrelated to the composition of adjacent veins and thus theseamphiboles are precipitates from fluids percolating into thedunite from the veins. Disseminated amphibole reflects the compositionof the percolating melt, which is similar to that of the associatedveins. KEY WORDS: mantle amphibole; Kerguelen; HFSE fractionation; mantle HFSE; mantle xenoliths     

Garnet Lherzolites from the Kaapvaal Craton (South Africa): Trace Element Evidence for a Metasomatic History

Kimberlites from the Kaapvaal craton have sampled numerous mantlegarnet lherzolites in addition to garnet harzburgites. Traceelement characteristics of constituent clinopyroxenes allowtwo groups of garnet lherzolites to be distinguished. Traceelement compositions of all clinopyroxenes are characterizedby enrichment in light rare earth elements (LREE) and largeion lithophile elements and by a relative depletion in Ti, Nb,Ta, and to a lesser extent Zr and Hf. However, the LREE enrichmentand the depletion in Nb and Zr (Hf) are less in the Type 1 clinopyroxenesthan in the Type 2 clinopyroxenes. Our study suggests that thetwo melts responsible for the metasomatic imprints observedin the two garnet lherzolite groups are highly alkaline maficsilicate melts. Type 1 clinopyroxenes that have trace elementsimilarities to those of PIC (Phlogopite–Ilmenite–Clinopyroxene)rocks appear to have crystallized from, or been completely equilibratedwith, the same melt related to Group I kimberlite magma. TheType 2 clinopyroxenes have trace element similarities to thoseof MARID (Mica– Amphibole–Rutile–Ilmenite–Diopside)rocks and are therefore probably linked to melt related to GroupII kimberlite magma. KEY WORDS: garnet lherzolites; Kaapvaal craton; mantle xenoliths; mantle metasomatism; trace elements     

Trace Element Residence and Partitioning in Mantle Xenoliths Metasomatized by Highly Alkaline, Silicate- and Carbonate-rich Melts (Kerguelen Islands, Indian Ocean)

Mantle xenoliths in alkaline lavas of the Kerguelen Islandsconsist of: (1) protogranular, Cr-diopside-bearing harzburgite;(2) poikilitic, Mg-augite-bearing harzburgite and cpx-poor lherzolite;(3) dunite that contains clinopyroxene, spinel phlogopite, andrarely amphibole. Trace element data for rocks and mineralsidentify distinctive signatures for the different rock typesand record upper-mantle processes. The harzburgites reflectan initial partial melting event followed by metasomatism bymafic alkaline to carbonatitic melts. The dunites were firstformed by reaction of a harzburgite protolith with tholeiiticto transitional basaltic melts, and subsequently developed metasomaticassemblages of clinopyroxene + phlogopite ± amphiboleby reaction with lamprophyric or carbonatitic melts. We measuredtwo-mineral partition coefficients and calculated mineral–meltpartition coefficients for 27 trace elements. In most samples,calculated budgets indicate that trace elements reside in theconstituent minerals. Clinopyroxene is the major host for REE,Sr, Y, Zr and Th; spinel is important for V and Ti; orthopyroxenefor Ti, Zr, HREE, Y, Sc and V; and olivine for Ni, Co and Sc. KEY WORDS: mantle xenoliths; mantle metasomatism; partition coefficients; Kerguelen Islands; trace elements     

Effect of hot desert weathering on the bulk‐rock iron isotope composition of L6 and H5 ordinary chondrites

Abstract– Although iron isotopes are increasingly used for meteorites studies, no attempt has been made to evaluate the effect of terrestrial weathering on this isotopic tracer. We have thus conducted a petrographic, chemical, and iron isotopic study of equilibrated ordinary chondrites (OC) recovered from hot Moroccan and Algerian Saharan deserts environment. As previously noticed, we observe that terrestrial desertic weathering is characterized by the oxidation of Fe‐Ni metal (Fe⁰), sulfide and Fe²⁺ occurring in olivine and pyroxene. It produces Fe‐oxides and oxyhydroxides that partially replace metal, sulfide grains and also fill fractures. The bulk chemical compositions of the ordinary chondrites studied show a strong Sr and Ba enrichment and a S depletion during weathering. Bulk meteoritic iron isotope compositions are well correlated with the degree of weathering and S, Sr, and Ba contents. Most weathered chondrites display the heaviest isotopic composition, by up to 0.1‰, which is of similar magnitude to the isotopic variations resulting from meteorite parent bodies’ formation and evolution. This is probably due to the release of isotopically light Fe²⁺ to waters on the Earth’s surface. Hence, when subtle Fe isotopic effects have to be studied in chondrites, meteorites with weathering grade above W2 should be avoided.     

Determination of Ruthenium,Palladium and Iridium in 27 In ternational Reference Silicate and I Ron-Formation Rocks,Ores and Related Materials By Isotope Dilution Inductively-Coupled Plasma Mass Spectrometry*

Ruthenium, palladium and iridium have been determined in 27 international reference rocks, ores and related materials by inductively-coupled plasma mass spectrometry using isotope dilution and sample introduction by solution nebulization and electrothermal vaporization, after chemical separation by co-precipitation with tellurium. The accuracy of the procedure is discussed by comparison of the results obtained with synthetic solutions and standard samples.