Coesite inclusions in diamonds of Yakutia

The results of the study of diamonds with inclusions of high-pressure modification of SiO₂ (coesite) by Raman spectroscopy are reported. It is established that the octahedral crystal from the Zapolyarnaya pipe is characterized by the highest residual pressure (2.7 ± 0.07 GPa). An intermediate value of this parameter (2.1 ± 0.07 GPa) was obtained for a crystal of transitional habit from the Maiskaya pipe. The minimal Raman shift was registered for coesite in diamond from the Komsomol’skaya–Magnitnaya pipe and provided a calculated residual pressure of 1.8 ± 0.03 GPa. The residual pressures for crystals from the placer deposits of the Kuoika and Bol’shaya Kuonamka rivers are 2.7 ± 0.07 and 3.1 ± 0.1 GPa, respectively. Octahedral crystals were formed in the mantle at a higher pressure than rhombododecahedral diamonds.     

Nature of diamonds in Yakutian eclogites: views from eclogite tomography and mineral inclusions in diamonds

We have performed dissections of two diamondiferous eclogites (UX-1 and U33/1) from the Udachnaya kimberlite, Yakutia in order to understand the nature of diamond formation and the relationship between the diamonds, their mineral inclusions, and host eclogite minerals. Diamonds were carefully recovered from each xenolith, based upon high-resolution X-ray tomography images and three-dimensional models. The nature and physical properties of minerals, in direct contact with diamonds, were investigated at the time of diamond extraction. Polished sections of the eclogites were made, containing the mould areas of the diamonds, to further investigate the chemical compositions of the host minerals and the phases that were in contact with diamonds. Major- and minor-element compositions of silicate and sulfide mineral inclusions in diamonds show variations among each other, and from those in the host eclogites. Oxygen isotope compositions of one garnet and five clinopyroxene inclusions in diamonds from another Udachnaya eclogite (U51) span the entire range recorded for eclogite xenoliths from Udachnaya. In addition, the reported compositions of almost all clinopyroxene inclusions in U51 diamonds exhibit positive Eu anomaly. This feature, together with the oxygen isotopic characteristics, is consistent with the well-established hypothesis of subduction origin for Udachnaya eclogite xenoliths. It is intuitive to expect that all eclogite xenoliths in a particular kimberlite should have common heritage, at least with respect to their included diamonds. However, the variation in the composition of multiple inclusions within diamonds, and among diamonds, from the same eclogite indicates the involvement of complex processes in diamond genesis, at least in the eclogite xenoliths from Yakutia that we have studied.     

The formation of peridotitic suite inclusions in diamonds

Olivine, orthopyroxene and garnet grains belonging to the peridotitic suite of mineral inclusions in natural diamonds typically show compositions poorer in Ca and Al and richer in Mg and Cr than the same minerals in peridotite nodules in kimberlite. Other features suggest the crystallisation of diamonds from magmas of kimberlitic affinities, and it is suggested that the genesis of peridotitic suite diamonds is linked with that of a CO₂-bearing magma. It is shown that the generation of kimberlitic magma from common garnet-peridotite (with 5 wt.% clinopyroxene) in the presence of CO₂ may rapidly remove by melting all Ca-rich solid phases (clinopyroxene and/or carbonate). Further melting may form liquids in equilibrium with olivine, orthopyroxene, and garnet with the distinctive compositions of the diamond inclusions. The amount of melting and CO₂ necessary for the loss of clinopyroxene (and/or carbonate) are estimated at approximately 5.0 wt.% and 0.5 wt.% respectively.     

The mineralogy of Ca-rich inclusions in sublithospheric diamonds

This paper discusses mineralogy of Ca-rich inclusions in ultra-deep (sublithospheric) diamonds. It was shown that most of the Ca-rich majoritic garnets are of metabasic (eclogitic) affinity. The observed variation in major and trace element composition is consistent with variations in the composition of the protolith and the degree of enrichment or depletion during interaction with melts. Major and trace element compositions of the inclusions of Ca minerals in ultra-deep diamonds indicate that they crystallized from Ca-carbonatite melts that were derived from partial melting of eclogite bodies in deeply subducted oceanic crust in the transition zone or even the lower mantle. The occurrence of merwinite or CAS inclusions in ultra-deep diamonds can serve as mineralogical indicators of the interaction of metaperidotitic and metabasic mantle lithologies with alkaline carbonatite melts. The discovery of the inclusions of carbonates in association with ultra-deep Ca minerals can not only provide additional support for their role in the diamond formation process but also help to define additional mantle reservoirs involved in global carbon cycle.     

Trace elements in sulfide inclusions from Yakutian diamonds

 Sulfide inclusions in diamonds may provide the only pristine samples of mantle sulfides, and they carry important information on the distribution and abundances of chalcophile elements in the deep lithosphere. Trace-element abundances were measured by proton microprobe in >50 sulfide inclusions (SDI) from Yakutian diamonds; about half of these were measured in situ in polished plates of diamonds, providing information on the spatial distribution of compositional variations. Many of the diamonds were identified as peridotitic or eclogitic from the nature of coexisting silicate or oxide inclusions. Known peridotitic diamonds contain SDIs with Ni contents of 22–36%, consistent with equilibration between olivine, monosulfide solid solution (MSS) and sulfide melt, whereas SDIs in eclogitic diamonds contain 0–12% Ni. A group of diamonds without silicate or oxide inclusions has SDIs with 11–18% Ni, and may be derived from pyroxenitic parageneses. Eclogitic SDIs have lower Ni, Cu and Te than peridotitic SDIs; the ranges of the two parageneses overlap for Se, As and Mo. The Mo and Se contents range up to 700 and 300 ppm, respectively; the highest levels are found in peridotitic diamonds. Among the in-situ SDIs, significant Zn and Pb levels are found in those connected by cracks to diamond surfaces, and these elements reflect interaction with kimberlitic melt. Significant levels of Ru (30–1300 ppm) and Rh (10–170 ppm) are found in many peridotitic SDIs; SDIs in one diamond with wustite and olivine inclusions and complex internal structures have high levels of other platinum-group elements (PGEs) as well, and high chondrite-normalized Ir/Pd. Comparison with experimental data on element partitioning between crystals of monosulfide solid solution (MSS) and sulfide melts suggests that most of the inclusions in both parageneses were trapped as MSS, while some high-Cu SDIs with high Pd±Rh may represent fractionated sulfide melts. Spatial variations of SDI composition within single diamonds are consistent with growth histories shown by cathodoluminescence images, in which several stages of growth and resorption have occurred within magmatic environments that evolved during diamond formation. Received: 5 July 1995 / Accepted: 21 February 1996     

Ar/Ar analyses of clinopyroxene inclusions in African diamonds: implications for source ages of detrital diamonds

Clinopyroxene inclusions in diamond contain elevated potassium contents and can potentially be dated by ⁴⁰Ar/³⁹Ar techniques. Previous ⁴⁰Ar/³⁹Ar studies of clinopyroxene inclusions contained in cleaved diamonds have suggested that argon, produced from the decay of potassium prior to eruption of the host kimberlite magma, diffuses to the diamond/clinopyroxene interface under mantle conditions. After intrusion and cooling below the closure temperature for argon diffusion, radiogenic argon is retained by the clinopyroxene inclusions. This behaviour complicates efforts to date diamond crystallisation events; however, extraction of inclusions from their host diamond should induce loss of all interface argon, thus raising the possibility of determining kimberlite emplacement ages. This possibility has important implications for constraining the source localities of detrital diamond deposits worldwide, with concomitant benefits to diamond exploration. To investigate this premise, ⁴⁰Ar/³⁹Ar laser probe results are presented for single clinopyroxene inclusions extracted from a total of fifteen gem-quality diamonds from the Mbuji-Mayi kimberlite in the Democratic Republic of Congo, and the Jwaneng and Orapa kimberlites in Botswana.Initial fusion analyses of clinopyroxene inclusions from Mbuji-Mayi diamonds yielded ages older than the time of host kimberlite intrusion, indicating partial retention of extraneous argon by the clinopyroxene inclusions themselves. Step-heating analyses of clinopyroxene inclusions from Orapa and Jwaneng diamonds produced older apparent ages from lower temperature steps and the ‘rim’ fragment of one Orapa inclusion. High temperature (fusion) analyses yielded younger apparent ages, commonly approaching the times of host kimberlite eruption. Total-gas integrated ⁴⁰Ar/³⁹Ar ages are mostly intermediate between the times of inferred diamond crystallisation and kimberlite eruption. Ca/K ratios for each sample are uniform across step-heating increments, indicating that age variations are not due to compositional, mineralogical or alteration effects. The favoured explanation for these results is partial retention of extraneous argon in primary and/or secondary fluid inclusions. This component is then preferentially outgassed in lower temperature heating steps, yielding older apparent ages.The partial retention of extraneous argon by clinopyroxene inclusions clearly restricts efforts to determine source ages for detrital diamond deposits. Results from individual samples must necessarily be interpreted as maximum source emplacement ages. Nonetheless, step-heating analyses of several clinopyroxene inclusions from a detrital diamond deposit may provide reasonable constraints on the ages of source kimberlites/lamproites; however minor age populations as well as those closely spaced in time, may be difficult to resolve.It is argued that the majority of older ⁴⁰Ar/³⁹Ar ages can be explained in terms of the partial retention of inherited argon, produced between the times of diamond crystallisation and kimberlite eruption. Although the presence of excess argon in some clinopyroxene inclusions cannot be excluded, available evidence (e.g. no excess argon in Premier eclogitic inclusions or potassium-poor inclusions) suggests that this is not a factor for most samples. Three possible mechanistic models are forwarded to account for the uptake of inherited (± excess) argon in fluid inclusions. The first envisages negligible interface porosity and diffusion of extraneous argon exclusively to primary fluid inclusions, which subsequently partially decrepitated during eruption, causing accumulation of argon at the diamond/clinopyroxene interface. The second model permits diffusive loss of extraneous argon to both the interface region and primary fluid inclusions. The third involves diffusion of extraneous argon to the interface region, with later entrapment of some interface argon in secondary fluid inclusions, produced by fracture/annealing processes active during eruption. The first model can account for all ⁴⁰Ar/³⁹Ar results, whereas the latter two mechanisms require the presence of an excess argon component to explain older integrated ages (up to 2.9 Ga) from two Jwaneng samples. Excess argon contamination would compromise efforts to determine diamond genesis ages using the ⁴⁰Ar/³⁹Ar dating technique. However, if the first model is valid, then the older ⁴⁰Ar/³⁹Ar integrated ages support previous Re-Os age results for the crystallisation of Jwaneng diamonds.     

The birth of the continents: new clues from inclusions in diamonds

Tiny inclusions found in diamonds may hold the clue to the origin of the Earth's continental crust. This is the new idea proposed by a group of Earth scientists from Australia and Russia studying a diamond pipe in Siberia.     

The trace element composition of silicate inclusions in diamonds: a review

On a global scale, peridotitic garnet inclusions in diamonds from the subcratonic lithosphere indicate an evolution from strongly sinusoidal REE_N, typical for harzburgitic garnets, to mildly sinusoidal or “normal” patterns (positive slope from LREE_N to MREE_N, fairly flat MREE_N–HREE_N), typical for lherzolitic garnets. Using the Cr-number of garnet as a proxy for the bulk rock major element composition it becomes apparent that strong LREE enrichment in garnet is restricted to highly depleted lithologies, whereas flat or positive LREE–MREE slopes are limited to less depleted rocks. For lherzolitic garnet inclusions, there is a positive relation between equilibration temperature, enrichment in MREE, HREE and other HFSE (Ti, Zr, Y), and decreasing depletion in major elements. For harzburgitic garnets, relations are not linear, but it appears that lherzolite style enrichment in MREE–HREE only occurs at temperatures above 1150–1200 °C, whereas strong enrichment in Sr is absent at these high temperatures. These observations suggest a transition from melt metasomatism (typical for the lherzolitic sources) characterized by fairly unfractionated trace and major element compositions to metasomatism by CHO fluids carrying primarily incompatible trace elements. Melt and fluid metasomatism are viewed as a compositional continuum, with residual CHO fluids resulting from primary silicate or carbonate melts in the course of fractional crystallization and equilibration with lithospheric host rocks.

Eclogitic garnet inclusions show “normal” REE_N patterns, with LREE at about 1× and HREE at about 30× chondritic abundance. Clinopyroxenes approximately mirror the garnet patterns, being enriched in LREE and having chondritic HREE abundances. Positive and negative Eu anomalies are observed for both garnet and clinopyroxene inclusions. Such anomalies are strong evidence for crustal precursors for the eclogitic diamond sources. The trace element composition of an “average eclogitic diamond source” based on garnet and clinopyroxene inclusions is consistent with derivation from former oceanic crust that lost about 10% of a partial melt in the garnet stability field and that subsequently experienced only minor reenrichment in the most incompatible trace elements. Based on individual diamonds, this simplistic picture becomes more complex, with evidence for both strong enrichment and depletion in LREE.

Trace element data for sublithospheric inclusions in diamonds are less abundant. REE in majoritic garnets indicate source compositions that range from being similar to lithospheric eclogitic sources to strongly LREE enriched. Lower mantle sources, assessed based on CaSi–perovskite as the principal host for REE, are not primitive in composition but show moderate to strong LREE enrichment. The bulk rock LREE_N–HREE_N slope cannot be determined from CaSi–perovskites alone, as garnet may be present in these shallow lower mantle sources and then would act as an important host for HREE. Positive and negative Eu anomalies are widespread in CaSi–perovskites and negative anomalies have also been observed for a majoritic garnet and a coexisting clinopyroxene inclusion. This suggests that sublithospheric diamond sources may be linked to old oceanic slabs, possibly because only former crustal rocks can provide the redox gradients necessary for diamond precipitation in an otherwise reduced sublithospheric mantle.     

Trace element abundance patterns of garnet inclusions in peridotite-suite diamonds

Individual, sub-calcic, chrome-pyrope crystals from Finsch and Kimberley diamonds, Finsch and Bultfontein kimberlite heavy mineral concentrate, and from diamondiferous harzburgite-dunite xenoliths from the Udachnaya kimberlite pipe were analyzed for rare earth elements (REE), Sc, Ti, and Zr with the ion microprobe. The abundances and abundance ratios of these trace elements including LREE enrichment and low Ti, together with high and variable Cr contents, are inconsistent with a simple equilibrium relationship between peridotite-suite garnet and silicate and carbonate liquids. It is suggested that the trace element abundance patterns represent a signature of ancient mantle metasomatism which preceded the formation of peridotite-suite garnet and diamond.     

Mineral inclusions in diamonds from the River Ranch kimberlite, Zimbabwe

More than 99% of mineral inclusions in diamonds from the River Ranch pipe in the Late Archean Limpopo Mobile Belt (Zimbabwe), are phases of harzburgitic paragenesis, namely olivine (Fo_92–93), orthopyroxene (Mg# = 93), G10 garnets and chromites. The diamond inclusion (DI) chemistry demonstrates a limited overlap with River Ranch kimberlite macrocrysts: the DI garnets are more Ca-undersaturated, and DI spinel and garnet are more Mg-rich. Most River Ranch diamond inclusions were equilibrated at T = 1080–1320 °C, P = 47–61 kbar, and f _O2 between IW and WM buffers. The P/T profile beneath the Limpopo Mobile Belt (LMB) is consistent with a paleo-heat flow of 41–42 mW/m², similar to calculations for Roberts Victor, but hotter than for the Finsch, Kimberley, Koffiefontein and Premier Mines. This is ascribed to the younger tectonothermal age of the LMB and its proximity to Late Archean oceans. Like diamond inclusions from all other kimberlites studied, the River Ranch DI have a lithospheric affinity and therefore indicate that an ancient, chemically depleted, thick (at least 200 km) mantle root existed beneath the Limpopo Mobile Belt 530–540 Ma ago. The mantle root might have developed beneath the continental Central Zone of the LMB as early as the Archean, and could be alien to the overthrust allochthonous sheet of the Limpopo Belt. Oxygen fugacity estimates for diamond inclusions at River Ranch are similar to other diamondiferous harzburgites beneath the Kaapvaal craton, indicating that the Kaapvaal mantle as a whole was well buffered and homogeneous with respect to f _O2 at the time of peridotitic diamond crystallization. Received: 11 January 1995 / Accepted: 10 June 1997     

Experimental investigation of the origin of majoritic garnet inclusions in diamonds

 Multianvil experiments were carried out at 10–15 GPa and 1600–1700 °C to match the compositions of majoritic garnet inclusions from diamonds, and to determine the compositions of other phases potentially coexisting with these inclusions in the source. Most experiments produced coexisting majoritic garnet, diopsidic clinopyroxene, one or more (Mg,Fe)₂SiO₄ polymorphs, and quenched carbonatic melt. The experimental garnets had relatively high Ca and Fe contents similar to the observed Ca and Fe contents of the inclusions. The resulting Si contents confirmed that the depth of origin of the inclusion with the highest Si content did not exceed 410 km, thus none of the majoritic garnet inclusions found so far originated in the transition zone (410–660 km). The evidence from inclusions and experiments is consistent with the presence of an eclogite layer occurring globally between 200 and 410 km. Compositional variations observed among more than 100 majoritic garnet inclusions with their Si content, which is a measure of pressure and depth, are consistent with the origin of the eclogite layer by crystal fractionation in a magma ocean. The compositions of olivine coexisting with majoritic garnet in the experimental products had the average Fe/(Fe + Mg) ratios between 0.16 and 0.28. Inclusions with such high Fe contents have not been found; the Fe/(Fe + Mg) ratio of the olivine inclusions in diamonds usually varies between 0.05 and 0.09. Hence, the mantle between 200 and 410 km may not contain olivine. In the absence of olivine, the discontinuity at 410 km is most likely a chemical boundary between the 200-km-thick eclogite layer and a more mafic transition zone. Received: 15 March 2001 / Accepted: 14 September 2001     

Rare and unusual mineral inclusions in diamonds from Mwadui, Tanzania

Syngenetic diamond inclusions from the Mwadui kimberlite reveal that an unusually fertile section of lithospheric mantle beneath the Central African Craton was sampled. This is shown by a very high ratio of lherzolitic to harzburgitic garnet inclusions (1:2) and low Mg/Fe-ratios in olivine and orthopyroxene. Geothermometry applied to the peridotitic inclusions indicates disequilibrium between non-touching inclusion pairs to be common. Disequilibrium between garnet-olivine and garnet-orthopyroxene pairs suggests successive iron enrichment during diamond formation, e.g. leading to the presence of harzburgitic garnet and lherzolitic olivine in the same diamond. Apart from the dominant peridotitic inclusion suite (88%), rare eclogitic inclusions occur (2%) and a number of uncertain paragenesis. Two diamonds, one with eclogitic garnets with moderate pyroxene solid solution and the other with a single ferro-periclase inclusion, suggest the contribution of a small sub-lithospheric component. The finding of the association Fe-FeO-Fe₃O₄ in one single diamond indicates diamond formation over a large range of f _O2 conditions, possibly along redox fronts. Steep compositional gradients may also be reflected by the joint occurrence of harzburgitic garnet and a SiO₂-phase in the same diamond. Alternatively the formation of the SiO₂-phase may be due to extreme carbonation of the peridotitic source. Further unusual findings include the exsolution of a silicate phase from magnetite inclusions, (i.e. primary solution of γ-olivine) and an ilmenite inclusion with an eskolaite (Cr₂O₃) component of 14.5 mol%, the latter together with harzburgitic paragenesis silicate inclusions. Received: 23 August 1997 / Accepted: 7 January 1998     

Mineral inclusions in diamonds: associations and chemical distinctions around the 670-km discontinuity

Three new mineral associations have been discovered within diamonds from the Juina district of Brazil. These include a previously unrecorded Na-Al-(Mg, Fe)SiO₃ phase associated with ferropericlase and the tetragonal almandine pyrope phase, TAPP. Also reported are an association of corundum with aluminous-pyroxene and an olivine composition phase associated with ferropericlase. The minerals in each association often occurred within the same diamonds in addition to being recovered from individual diamonds in different combinations. High-pressure experimental data indicate that these associations formed at different depths within a region ca. 60 km on either side of the upper-mantle/lower-mantle boundary. Mineral compositions show that for the regions sampled, the deep transition zone and lower mantle are chemically distinct and inhomogeneous. Importantly, in the shallow lower mantle, Al is not solely accommodated within perovskite-structured (Mg, Fe)SiO₃ as some recent experimental studies have suggested.     

Mineral inclusions in diamonds from the Sputnik kimberlite pipe, Yakutia

The Sputnik kimberlite pipe is a small “satellite” of the larger Mir pipe in central Yakutia (Sakha), Russia. Study of 38 large diamonds (0.7-4.9 carats) showed that nine contain inclusions of the eclogitic paragenesis, while the remainder contain inclusions of the peridotitic paragenesis, or of uncertain paragenesis. The peridotitic inclusion suite comprises olivine, enstatite, Cr-diopside, chromite, Cr-pyrope garnet (both lherzolitic and harzburgitic), ilmenite, Ni-rich sulfide and a Ti-Cr-Fe-Mg-Sr-K phase of the lindsleyite-mathiasite (LIMA) series. The eclogitic inclusion suite comprises omphacite, garnet, Ni-poor sulfide, phlogopite and rutile. Peridotitic ilmenite inclusions have high Mg, Cr and Ni contents and high Nb/Zr ratios; they may be related to metasomatic ilmenites known from peridotite xenoliths in kimberlite. Eclogitic phlogopite is intergrown with omphacite, coexists with garnet, and has an unusually high TiO₂ content. Comparison with inclusions in diamonds from Mir shows general similarities, but differences in details of trace-element patterns. Large compositional variations among inclusions of one phase (olivine, garnet, chromite) within single diamonds indicate that the chemical environment of diamond crystallisation changed rapidly relative to diamond growth rates in many cases. P-T conditions of formation were calculated from multiphase inclusions and from trace element geothermobarometry of single inclusions. The geotherm at the time of diamond formation was near a 35 mW/m² conductive model; that is indistinguishable from the Paleozoic geotherm derived by studies of xenoliths and concentrate minerals from Mir. A range of Ni temperatures between garnet inclusions in single diamonds from both Mir and Sputnik suggests that many of the diamonds grew during thermal events affecting a relatively narrow depth range of the lithosphere, within the diamond stability field. The minor differences between inclusions in Mir and Sputnik may reflect lateral heterogeneity in the upper mantle.     

Mineral inclusions in fibrous diamonds: constraints on cratonic mantle refertilization and diamond formation

We analyzed mineral microinclusions in fibrous diamonds from the Wawa metaconglomerate (Superior craton) and Diavik kimberlites (Slave craton) and compared them with published compositions of large mineral inclusions in non-fibrous diamonds from these localities. The comparison, together with similar datasets available for Ekati and Koffiefontein kimberlites, suggest a general pattern of metasomatic alteration imposed on the ambient mantle by formation of fibrous diamond. Calcium and Fe enrichment of peridotitic garnet and pyroxenes and Fe enrichment of olivine associated with fibrous diamond-forming fluids contributes to refertilization of the cratonic mantle. Saline—carbonatitic—silicic fluid trapped by fibrous diamonds may represent one of the elusive agents of mantle refertilization. Calcium enrichment of peridotitic garnet and pyroxenes is expected in local mantle segments during fibrous diamond production, as Ca in the carbonatitic fluids is deposited into the surrounding mantle when oxidized carbon is reduced to diamond. Harzburgitic garnet evolves towards Ca-rich compositions even when it interacts with Ca-poor saline fluids. An unusual trend of Mg enrichment to Fo_95–98 is observed in some olivine inclusions in Wawa fibrous diamonds. The trend may result from the carbonatitic composition of the fluid that promotes crystallization of magnesian olivine and preferentially oxidizes the fayalite component. We propose a generic model of fibrous and non-fibrous diamond formation from carbonatitic fluids that explains enrichment of the mantle in mafic magmaphile and incompatible elements and accounts for locally metasomatized compositions of diamond inclusions.     

A low-temperature kinetic study of the exsolution of pentlandite from the monosulfide solid solution using a refined Avrami method

A refined Avrami method, that assumes that the activation energy is a function of reaction extent y, was used to analyze the kinetics of the exsolution of pentlandite from mss/pyrrhotite (bulk composition, (Fe_0.77Ni_0.19)S) over the temperature range 473 to 573 K. The experimental results show the reaction rates vary from 1.6 × 10⁻⁵ to 5.0 × 10⁻⁷ s⁻¹ at 473 K and from 9.4 × 10⁻⁵ to 4.1 × 10⁻⁷ s⁻¹ at 573 K. Examination of exsolution textures indicated that the mechanism of exsolution did not change significantly over the temperature range investigated. The activation energy (E_a) decreases from 49.6 to 20.7 kJ mol⁻¹ over the course of the reaction. The decrease in E_a with y is related to the change in the dominant factor of pentlandite exsolution, from nucleation dominant at the beginning to metal ion diffusion dominant at the end. The classic Avrami method provides average values of kinetic parameters for the overall solid-state reaction while the refined Avrami method provides more a detailed indication of the variation of kinetic parameters over the course of the reaction. Previously published kinetic data for the exsolution of pentlandite from mss/pyrrhotite are reevaluated using the refined Avrami method.