The partitioning of a large suite of trace elements between biotite and water-saturated granitic melt was measured at 2 kbar and 700—800 ˚C. To reach equilibrium and to grow biotite crystals large enough for analysis, runs usually lasted from 30 to 45 days. In every charge, a few trace elements were initially doped at the 0.1—0.5 wt. % level and analyzed by electron microprobe after the run. First-row transition metal ions are highly compatible in biotite with Dbiotite/melt of 17 for Ti, 35 for V, 47 for Co, 174 for Ni, and 5.8 for Zn. A very notable exception is Cu with Dbiotite/melt < 0.9. This is likely one of the reasons why Cu is enriched together with Mo (Dbiotite/melt = 0.29) in porphyry deposits associated with intermediate to felsic plutons, while the other transition metals are not. Both Nb and Ta are mildly compatible in biotite with Dbiotite/melt being larger for Nb (3.69) than for Ta (1.89). Moderate (15—30%) biotite fractionation would be sufficient to reduce the Nb/Ta ratio from the chondritic value to the range observed in the continental crust. Moreover, the strong partitioning of Ti into biotite implies that already modest biotite fractionation suppresses the saturation of Ti-oxide phases and thereby indirectly facilitates the enrichment of Ta over Nb in the residual melt. The heavy alkalis, alkaline earths, and Pb are only mildly fractionated between biotite and melt (Dbiotite/melt = 3.8 for Rb, 0.6 for Cs, 0.6 for Sr, 1.8 for Ba, 0.7 for Pb). The rare earth elements are generally incompatible in biotite, with a minimum for Dbiotite/melt of 0.03–0.06 at Gd, Tb, and Dy, while both the light and heavy rare earths are less incompatible (e.g. Dbiotite/melt = 0.6 for La and 0.3 for Yb). This behavior probably reflects a partitioning into two sites, the K site for the light rare earths and the octahedral Mg site for the heavy rare earths. There is no obvious dependence of the rare earth partition coefficients on tetrahedral Al in the biotite, presumably because charge balancing by cation vacancies is possible. Allanite was found as run product in some experiments. For the light rare earths, Dallanite/melt is very high (e.g. 385 to 963 for Ce and Nd) and appears to increase with decreasing temperatures. However, the rather high solubility of allanite in the melts implies that it likely only crystallizes during the last stages of cooling of most magmas, except if the source magma is unusually enriched in rare earths.
Biotite K(Mg,Fe)3(OH)2AlSi3O10 is a sheet silicate and a common and abundant mineral in igneous rocks of intermediate to felsic composition, particularly in plutonic environments (e.g. Speer 1984). It may accommodate various trace elements, either on the 12-coordinated K site (Bailey 1984) or on the octahedral Mg and Fe site. Crystallization of biotite, therefore, likely has a strong effect on the fractionation and enrichment of trace elements in such magmas. Since most porphyry copper, porphyry tin, and pegmatite-related ore deposits are associated with intermediate to felsic plutons (e.g. Sillitoe 2010), understanding the effects of biotite fractionation on the behavior of trace elements in these magmas is also of considerable interest for economic geology.
Rather surprisingly, the partitioning of trace elements between biotite and felsic to intermediate melts is only poorly studied. A possible reason for this could be the difficulty to grow biotite crystals large enough for chemical analysis in laboratory experiments; since biotite typically forms thin platelets, the limited thickness of these crystals may pose severe analytical problems. A notable earlier experimental study is that of Icenhower and London (1995), who measured the partition coefficients of Li, Rb, Cs, Sr, Ba, and F between biotite and a peraluminous silicic melt, using a mixture of natural biotite with other minerals as starting material. Under high-pressure conditions relevant for subduction zones (25–45 kbar), the partitioning of Nb, Ta, Rb, Sr, Cs, and Ba between biotite and silicic melts was studied by Stepanov and Hermann (2013) and Stepanov et al. (2016). Partition coefficients derived from the analysis of biotite phenocrysts and coexisting rhyolitic glass from natural volcanics were reported by Mahood and Hildreth (1983), Nash and Crecraft (1985), and by Ewart and Griffin (1994). Bea et al. (1994) reported biotite/leucosome partition coefficients from a migmatite.
In this study, we have investigated the partitioning of a large suite of trace elements between biotite and granitic melts at 2 kbar and 700–800 ˚C under water-saturated conditions. Biotite crystals were grown by crystallization from the melt. Trace elements investigated include the rare earths, high-field strength elements, large ion lithophile elements, as well as a large suite of transition metals that are relevant for the formation of ore deposits. To grow crystals large enough, very long run durations of 30–45 days were used. Most trace elements were doped at the level of several 1000 ppm and subsequently analyzed by electron microprobe.
Synthetic glasses were used as starting materials in all experiments. The nominal composition of the glasses corresponded to a mixture of 26.4 wt. % quartz, 30.1 wt. % albite, 18.8 wt. % potassium feldspar, 8.4 wt. % anorthite, 15.3 wt.% biotite KMg1.5Fe1.5(OH)2AlSi3O10, and typically a total of about 1 wt. % of a small set of trace element oxides. Individual trace elements were doped at the 1000 to 5000 ppm level of the oxide. The sets of trace elements doped were chosen such that overlapping X-ray emission lines in the subsequent microprobe analysis and the precipitation of unwanted accessory phases were avoided.
Starting materials were prepared by mixing high-purity (usually 99.9 wt. % or higher) oxides, hydroxides or carbonates of the respective elements in the desired proportion for 30 min under ethanol in an automated ball mill. After drying, the sample was transferred into a platinum crucible and during 48 h slowly heated to 1100 ˚C in an electrical furnace to decompose the carbonates and hydroxides. The sintered product was then ground in a ball mill. The resulting powder was then again transferred into a platinum crucible and rapidly heated to 1600 ˚C where it remained for two hours. Quenching of the crucible in water yielded a dark glass, which was ground up and used as starting material. The homogeneity of the glass was checked by electron microprobe. Microprobe analyses of all starting glasses used in the experiments are compiled in the supplementary online material (Table S1). SiO2 contents range from about 68 to 70 wt. % and the bulk compositions are near the border between typical dacites and rhyolites.
Experiments in cold-seal pressure vessels
About 30 to 45 mg of the starting glass powder (grain size < 10 m) were loaded together with 3 to 5.6 mg of doubly distilled water into gold capsules (25 mm long, 2.38 mm outer diameter, 0.13 mm wall thickness) and sealed by arc welding. All capsules were checked for leaks by heating them over night in a drying furnace to 150 ˚C. Only capsules that showed negligible (< 0.1 mg) weight loss during this test were used for experiments. All experiments were carried out at 2 kbar and 700–800 ˚C in externally heated, horizontal cold-seal vessels made of Ni-based super alloys (Rene 41 or Nimonic 105). The pressure medium was water, which together with a Ni filler rod and the Ni-rich alloy buffers oxygen fugacity close to the Ni–NiO buffer. All runs were first heated to 830 ˚C for 2 days to homogenize the charge. Afterwards, temperature was lowered to the desired run conditions, where the samples remained for 30–45 days. At the end of the run, the autoclaves were isobarically quenched to room temperature by removing them from the furnace and blowing cold air against them. Room temperature as reached within 10–15 min.
Investigation of run products
After the runs, the sample capsules were cleaned, dried, and weighed. They usually had gained some weight due to alloying with Ni, which diffused through the entire capsule wall and caused a noticeable contamination of the charge with Ni. Capsules were then pierced, dried again at 150 ˚C and weighed afterwards to detect a weight loss due to the presence of an excess H2O vapor phase. The capsules were then opened and a small fraction of the contents was ground up to a fine powder. Phases were identified by X-ray diffraction using a Philips PW 1050/25 X-ray powder diffractometer operating with Cu K∝ radiation, a focusing germanium monochromator and a position sensitive detector.
The remaining sample was mounted in epoxy resin and polished. Major element and trace element concentrations were measured by electron microprobe. The instruments used were a JEOL 8900 microprobe at the University of Tübingen and a JEOL 8200 instrument at Bayerisches Geoinstitut in Bayreuth. Analyses were carried out with an accelerating voltage of 20 kV and a beam current of 70 nA. For analyzing the glasses, a 20 μm defocused beam was used, while for the crystalline phases, the beam was focused. For major elements, the counting time was typically 30 s on peak and 15 s on background (6 s and 3 s, respectively, for Na in glasses). For trace elements, counting times were increased up to 180 s. The detection limit for most trace elements under the conditions specified is near 50 ppm. For the rare earth elements, the synthetic glass standards described by Duc-Tin and Keppler (2015) were used. The pure metals were used as standards for Co, Cr, Cu, Mo, Ni, Mo, Pb, V, and Zn. SrTiO3 was used as standard for Sr and Ti, BaSO4 for Ba, natural pollucite for Rb and Cs, ZrO2 for Zr, Li2Nb2O5 for Nb, Li2Ta2O6 for Ta, and CaWO4 for W. Trace element concentrations in glasses, biotite, and allanite reported here (e.g. Table 1) are averages of 5—15 individual electron microprobe analyses.
The experimental results are summarized in Table 1. Microprobe analyses of coexisting phases (quenched melt, biotite, and allanite) are compiled in Tables S2–S4 in the supplementary online material. All run products contained a quenched melt phase in the form of a glass, a quenched H2O-rich vapor phase (as indicated by weight loss after piercing and drying the capsule), abundant biotite crystals, as well as some other crystalline phases. A typical image of a run product is shown in Fig. 1. The quenched glasses were found to be chemically homogeneous upon microprobe analysis and the crystalline phases often showed well-developed crystal faces, consistent with chemical and textural equilibrium. Biotite was always the most abundant crystalline phase, occurring in platelets with a thickness up to 8 μm, while the other dimensions often exceeded 100 μm. The largest crystals were observed in the runs at 750–800 ˚C. Within the same charge, larger crystals often appeared near vapor bubbles (see Fig. 1), which may indicate some catalytic effect of the vapor on crystal growth (i.e. by dissolution of material from the melt in the vapor and re-precipitation in biotite). At lower temperatures, the size of the crystals decreased, which sometimes made microprobe analyses difficult. The average composition of biotite was approximately (K0.7Na0.1Ca0.02)(Mg1.2Fe0.6Al0.6Ni0.2)(Si3.4Al0.6)O10(OH)2. The Ni content is due to contamination by Ni diffusing from outside into the capsule. There is, however, a considerable variation in biotite compositions; for example, the Mg number (i.e. Mg/(Mg + Fe) in molar units), ranges from about 0.5 to 0.75, see supplementary Table S3.
Amphibole with a hornblende-like composition was found in most charges. It typically occurred as isolated, relatively large (50 μm) euhedral crystals with an approximate composition of (Na0.4K0.1)(Ca1.7Fe0.3)(Mg3.3Fe1.3Al0.4)(Si7.0Al1.0)O22(OH)2. Clinopyroxene (augite) was also frequently observed, as relatively large euhedral crystals at 750—800 ˚C and as thin elongated needles at lower temperatures. The average composition was approximately (Ca0.8Na0.04K0.02Fe0.2)(Mg0.7Al0.1Fe0.2)Si2O6. The abundance of both amphibole and clinopyroxene generally increased with temperature. In contrast to this, the abundance of plagioclase generally decreased with temperature. Plagioclase crystals often appeared as clusters within the sample; their average composition was (Na0.6Ca0.4)(Al1.4Si2.6)O8. Magnetite with approximate composition (Fe0.85Mg0.07K0.004Ca0.002Na0.002)(Fe1.9Al0.14Si0.01)O4 was an accessory phase, particularly in the runs at higher temperatures. The presence of magnetite is consistent with the relatively oxidized conditions near the Ni–NiO buffer. Allanite was only observed in some runs doped with light rare earth elements. It typically occurred as euhedral crystals, sometimes larger than 100 μm. Whenever allanite was present, only little or no amphibole crystallized. A typical composition of allanite in a neodymium-doped run was (Ca1.0Nd0.8K0.004Na0.003)(Al1.6Fe1.0Mg0.4)Si3O12(OH). However, allanite was not observed in all runs doped with light rare earth (e.g. run 29/M31 doped with La). Very likely, some allanite had formed in these experiments as well, it was just not detected because the few small crystals were not intersected by the microprobe slice. This may also apply to some other accessory minerals, such as zircon, which should have formed in the experiments carried out with Zr-doped starting material (e.g. 33/M71), but was likely not detected because of its small abundance.
Biotite/melt partitioning of alkalis, alkaline earth elements, and Pb
Measured partition coefficients of all trace elements as well as of some major elements are compiled in Table 2. In most cases, the numbers given are averages of several experiments. Figure 2 shows the biotite/melt partition coefficients of the alkalis (Na+, K+, Rb+, Cs+), alkaline earths (Ca2+, Sr2+, Ba2+) and of Pb2+ as a function of ionic radius. Due to their large size, these elements are expected to partition into the 12-coordinated K site of biotite. Accordingly, the partition coefficients are plotted versus the ionic radii for 12-fold coordination, which are about 0.25 Å larger than the more commonly used radii for octahedral coordination (Shannon 1976). Also, for consistency with most of previous publications on trace element partitioning, we use the traditional ionic radii given by Shannon (1976), not the “crystal radii” from the same publication, which for cations would be 0.14 larger than the traditional ionic radii.
The ions K+, Rb+, and Ba2+ are mildly compatible in biotite, while Na+, Cs+, and Sr2+ are mildly incompatible. The most incompatible of these elements is Ca2+. The behavior of the alkalis is quite well described by a Brice-type lattice strain model (Brice 1975; Blundy and Wood 1994; Wood and Blundy 1997) with
where Di is the Nernst partition coefficient of element i, D0 is the partition coefficient for an ion of ideal radius r0 for the given site, E is Youngs modulus for the site, NA is Avogadro´s number, R is the gas constant and T is absolute temperature. For fitting this equation, T was always assumed to be 800 ˚C. For the alkali ions, the fit is quite well constrained and yields the parameters r0 = 1.67 Å ± 0.01 Å, D0 = 3.75 ± 0.5, and E = 527 kbar ± 39 kbar. The uncertainties given are estimated. Since there are only four experimental data to constrain three variables, a true evaluation of standard deviations is not possible. The value of E is quite comparable to that found for alkali ions in feldspars and pyroxenes (Blundy and Wood 1994), while r0 is considerably larger, as expected for the large 12-coordinated K site in biotite.
A possible Brice fit for the alkaline earth ions Ca2+, Sr2+, Ba2+, and for Pb2+ with r0 = 1.57 Å, D0 = 1.88, and E = 1456 kbar is also shown in Fig. 2. This fit is, however, not unique and different solutions with only moderately larger deviations from the experimental data would be possible. Notably, r0 is smaller than for the univalent cations. Small deviations in the ideal ionic radius for ions of different charge entering the same structure are possible and have been observed previously (e.g. Blundy and Wood 1994). However, in the mica structure, there is the additional possibility that the size of the interlayer K site may indeed change in response to cation substitutions. In normal biotite, the K ion is sandwiched in 12-fold coordination between two six-membered silicate rings of the tetrahedral layer. However, in other micas, notably the brittle micas containing Ca2+ in the interlayer, the silicate tetrahedra may rotate such that the size of the interlayer site is reduced to a smaller, sixfold coordinated site (Guggenheim 1984). If such an effect happened locally upon substitution of a divalent cation in the interlayer site of biotite, the difference in r0 between the alkali and alkali earth ions could perhaps be real. The partition coefficient of Pb2+ is slightly below that expected from the Brice fit. This may be due to the unusual electronic configuration of this ion with a lone electron pair.
Biotite/melt partitioning of transition metals
Partition coefficients for the transition metals are shown in Fig. 3a for the divalent ions and in Fig. 3b for the ions with higher oxidation states, between + 3 and + 6. The transition metals are expected to substitute into the octahedral Mg site of the mica structure. The partitioning of the divalent ions may be described by a Brice model with r0 = 0.62 Å, D0 = 183, and E = 4256 kbar. This model predicts the partitioning of Mg2+ and Fe2+ well, while Ni2+ and Co2+ are slightly above the fitted curve in Fig. 3a. This deviation is, however, expected from crystal field effects. Both Ni2+ and Co2+ have a high octahedral site preference energy, which means that the energies of the d electrons will be lowered in an octahedral environment as compared to a tetrahedral environment (e.g. Burns 1993). In silicate melts, these ions partially occupy tetrahedral sites (Keppler and Bagdassarov 1999), such that the partitioning into the octahedral site of biotite should yield an additional reduction of free energy, beyond that predicted by a lattice strain model. On the other hand, crystal field effects are absent for Mg2+ and of minor importance for Fe2+. However, at the redox conditions of the experiments, some of the iron is also expected to be in the Fe3+ oxidation state and the partition coefficient of iron measured does not reflect the behavior of Fe2+ alone. According to available calibrations, the fraction of iron in the ferric oxidation state in the melts from our experiments may be in the order of 10% (Gaillard et al. 2001, Wilke et al. 2001).
Both Zn2+ and Cu2+ fall below the predicted curve for the divalent transition metal ions in Fig. 3a. For Zn2+, this may be an experimental artifact. The Zn partitioning data are poorly reproducible, ranging from 0.9 to 15.6 in seven separate experiments. The higher end of this range is close to that expected from the Brice fit of the other divalent ions. A possible explanation for the strong scatter of the Zn partitioning data could be some kinetic effects related to Zn partitioning into magnetite as gahnite (Zn spinel) component. As one may see from Fig. 1, biotite crystals often occur close to locations that contain small crystals of magnetite; early crystallization of magnetite could have locally depleted the Zn concentration in the melt, such that relatively Zn-poor biotite crystallized, without reaching full equilibrium with the entire melt reservoir.
The strong deviation of Cu from the curves of the divalent transition metal ions is most likely real and probably reflects the fact that most Cu in the melt may not be in the Cu2+, but in the Cu+ oxidation state. For reasons of local charge balance, Cu+ may not easily substitute into the Mg site of biotite, while the ionic radius of Cu+ (0.77 Å for octahedral coordination) is far too low for the K site. If one assumed completely incompatible behavior of Cu+, the data in Fig. 3a would suggest that only a few % of the copper in the melt is in the 2 + oxidation state, as the partition coefficient of Cu is nearly two orders of magnitude below that predicted from the strain model for the divalent cations. This estimate is in good qualitative agreement with XANES data on the oxidation state of copper in silicate melts (Miller et al. 2019). In reality, the biotite/melt partition coefficient of Cu may be even lower than the value of 0.9 ± 0.2 reported here, because very likely some copper from the melt was absorbed into the gold of the capsule during the course of the experiments. This is obvious, because the Cu concentrations measured in the quenched melt were orders of magnitude below the initial doping level of copper into the starting material (0.5 wt. % CuO) and there is no other phase present in these samples that could have enriched Cu. Copper loss from the melt to the Au capsule is expected to occur during the entire experiment, while Cu diffusion in biotite may be too slow to fully re-equilibrate the biotite with the melt. Therefore, early formed biotite may have been in equilibrium with much higher Cu concentrations in the melt than those measured after the experiments. The Cu partition coefficients reported here are, therefore, only upper limits of the real values, which may well be one order of magnitude lower.
For the transition metal ions with oxidation states ranging from 3 + to 6 + (Fig. 3b) not enough data are available for constructing a lattice strain model for the various oxidation states. The partition coefficients shown in Fig. 3b are, however, consistent with an ideal substitution radius near 0.62 Å as for the divalent ions. With increasing ionic charge, the parabolas of the Brice fit should become more narrow, which is also qualitatively consistent with the data. While V3+ and Ti4+ are highly compatible in biotite, Cr3+, Nb5+, and Ta5+ are only moderately compatible, while Zr4+ and Mo6+ are incompatible. The incompatibility of Zr4+ is likely related to its relatively large ionic radius. Somewhat surprising is the behavior of Mo6+, in particular, the very strong apparent fractionation between Mo6+ and W6+. A possible explanation for the different behavior of Mo and W could be a difference in oxidation state. However, available XANES data and thermodynamic models suggest that near the Ni-NiO buffer, both Mo and W should be in the + 6 oxidation state, the + 4 state becoming important only at much lower oxygen fugacities (Farges et al. 2006, O´Neill et al. 2008, Righter et al. 2016). A possibility could perhaps be the stabilization of Mo5+ in the melt (Farges et al. 2006), as this oxidation state is much more stable for Mo than for W. Direct evidence for this hypothesis, however, is lacking.
Biotite/melt partitioning of rare earth elements
The rare earth elements are generally incompatible in biotite. The erbium data (Table 2) appear anomalous compared to all other REE data and are not further considered. Possibly, the erbium measurements were affected by some peak overlap with emission lines of Fe. As shown in Fig. 4, La has the highest partition coefficient among the rare earths (0.61 ± 0.15); the partition coefficients for the heavier REE first decrease to a minimum at Gd (0.041 ± 0.008) and the increase again to Lu (0.33 ± 0.14). This observation suggests that the rare earths partition into two different sites, with the light REE preferring the larger K site, while the heavy REE prefer the smaller Mg site. A possible Brice fit to the measured partition coefficients involving two different sites is shown in Fig. 4. The parameters used for the K site are r0 = 1.04 Å, D0 = 0.57, and E = 8289 kbar, for the Mg site r0 = 0.80 Å, D0 = 0.52, and E = 3268 kbar. Due to the scatter of the experimental data and the contribution from two different sites, these fit parameters are, however, not well constrained and they should be considered only as one of a range of possible solutions. Moreover, to produce a diagram as in Fig. 4 and to calculate a fit involving two different sites, a unique ionic radius, in this case for octahedral coordination, had to be assigned to every rare earth ion. However, as noted above, for the large K site, radii for 12-fold coordination may be more appropriate. Those radii would be 0.29–0.33 Å larger than those for octahedral coordination.
The substitution of trivalent rare earth elements into either the K site or the Mg site requires some charge compensation by coupled substitutions or by vacancies. For clinopyroxenes, it is well established that the substitution of trivalent rare earth elements for Ca2+ is greatly enhanced by the simultaneous substitution of Al3+ for Si4+ on the tetrahedral site (e.g. Gaetani and Grove 1995; Schosnig and Hoffer 1998; Hill et al. 2000). We have therefore investigated whether a similar relationship exists for biotite. However, while the number of tetrahedral Al atoms in biotites from our experiments ranges from about 0.6 to 1 per formula unit of biotite (with four tetrahedral cations), no clear correlation of the rare earth partition coefficients with tetrahedral Al was observed. This may be related to the fact that in biotite, several substitutions are possible to compensate for excess cation charges, including vacancies in both the K site and the Mg site. While such vacancies are energetically unfavorable in many silicates, such as the pyroxenes, the mica structure easily accepts them. In the dioctahedral micas, such as muscovite KAl2(OH)2AlSi3O10, only two out of three octahedral sites are filled with Al3+, in contrast to biotite, where all three sites are occupied by Mg2+. Vacancies in the K site are common in clay minerals. Indeed, the average composition of biotites synthesized in this study, approximately (K0.7Na0.1Ca0.02)(Mg1.2Fe0.6Al0.6Ni0.2)(Si3.4Al0.6)O10(OH)2, suggests some vacancies both on the K and on the Mg sites, which would readily allow charge compensation for trivalent rare earth elements.
Allanite was found as accessory phase in some runs doped with light rare earths (Fig. 1). It was not detected in all of those runs, however, this does not necessarily mean that it was absent in some experiments. Rather, being an accessory phase, it may have been overlooked because the studied sections may accidentally have failed to expose some allanite grains. Data on trace element partitioning between allanite and melt and on the solubility of allanite are compiled in Table 3. The melt compositions given in Table 3 were measured close to allanite grains and they may sometimes slightly deviate from the melt compositions for biotite partitioning given in Table 1. The deviations are, however, very small and usually within analytical error, consistent with the overall homogeneity of the samples.
The light rare earth elements strongly partition into allanite. According to Gieré and Sorensen (2004), they occupy the 11-coordinated A sites in the structure. Of the other elements studied (Table 3), only Cs and Zr are mildly compatible in allanite, while K, Na, and Nb are incompatible. Figure 5 shows the allanite/melt partition coefficient of Ce, Pr, Nd, and Er as function of ionic radius for tenfold coordination. The data at 800 ˚C are well described by a Brice fit with r0 = 1.27 Å, D0 = 400, and E = 2155 kbar. Figure 5 also suggests that Dallanite/melt of the light rare earths strongly increases with decreasing temperature. However, inspection of the raw data in Table 3 shows that this effect is actually not properly described by the term “partitioning”. Since the light rare earths are a stoichiometric main constituent of allanite, their concentration in allanite is essentially constant, while the concentration in the coexisting silicate melt changes as function of temperature. This behavior is better described as a change of allanite solubility (as expressed by equilibrium rare earth concentration) in the silicate melt. Figure 6 shows the solubility of Ce-, Pr-, and Nd-rich allanite as a function of temperature. Solubility is expressed as the concentration of dissolved REE2O3 in wt. %. The temperature effect is remarkably strong, with a temperature decrease by just 25 ˚C reducing the solubility by a factor of two. The slope of the regression line shown in Fig. 6 corresponds to an enthalpy of dissolution of 237 kJ/mol.
Comparison with previous studies
As noted above, only very few experimental data on biotite/melt partitioning are available. The results of Icenhower and London (1995) on Rb (Dbiotite/melt ~ 2) and Cs (0.27–0.49) are very similar to those of the present study and to Stepanov et al. (2016). For Ba, they observed a strong temperature dependence of the partition coefficients with the data at highest temperatures (750 ˚C, Dbiotite/melt ~ 6) being comparable to those observed here. Only for Sr, the reported biotite/melt partition coefficients appear rather low (0.03–0.06), which may perhaps reflect some equilibration problems in their study. The partition coefficients calculated from coexisting biotite and glass phase from the Bishop Tuff by Mahood & Hildreth (1983) are often remarkably similar to those measured in the current study, e.g. for Rb (4.3 versus 3.8 reported here), Cs (3.1 vs. 0.62), Ba (7 vs. 1.79), Ta (1.35 vs. 1.89), Cr (3.7 vs. 2.8), Co (86 vs. 47), and Zn (19 vs. 5.8). Notably, Mahood & Hildreth also observed a minimum in the partition coefficients of the middle rare earths, as in this study, although the absolute biotite/melt partition coefficients of the REE observed by them tend to be higher than in the present study (e.g. 3.4 vs. 0.61 for La). The latter effect may perhaps be related to the extremely silica-rich bulk composition of the Bishop Tuff (up to 77 wt. % of SiO2, versus ~ 69% in the starting material of the current experiments). The data of Nash and Crecraft (1985) obtained from coexisting biotite and glass from rhyolites and rhyodacites of Twin Peaks, Utah also show many similarities with the results of the current study, particularly for Nb, Ta, Zr, alkalis and alkaline earths. On the other hand, the biotite/melt partition coefficients from coexisting biotite and glass phase reported by Ewart and Griffin (1994) show a very large scatter for the same element and are not further discussed here. The overall biotite/leucosome partition coefficients of the rare earths observed by Bea et al. (1994) in a migmatite are comparable in order of magnitude to those observed in our study, but they do not show a clear minimum at the middle rare earths. Previous measurements of biotite/melt partition coefficients of elements not covered in this study include data for Be (0.39—0.54, Evensen and London 2002) and In (mostly around 5, Gion et al. 2018).
Aside from biotite, amphibole is the most prominent mafic mineral fractionating in hydrous intermediate to felsic magmas. It is, therefore, useful to compare the effect of those two minerals on trace element partitioning. Amphibole/melt partition coefficients are known to be strongly dependent on melt composition and only relatively few studies have been carried out on intermediate to silicic magmas, including those of Klein et al. (1997), Hilyard et al. (2000), and Nandedkar et al. (2016). All studies agree that the effect of amphibole on rare earth partitioning is nearly complementary to that of biotite: Damphibole/melt has a maximum at the middle rare earth near Dy, with values that are significantly above unity. While among all the rare earths, La has the highest mineral/melt partition coefficient for biotite, it is the least compatible rare earth in amphibole, due to the absence of a large site comparable to the K site in mica. Since the middle rare earths are compatible in amphibole, while all rare earths are incompatible in biotite, amphibole fractionation will usually have the stronger effect on rare earth abundance patterns in evolved magmas. However, for the high-field strength elements, the situation is different. These elements appear to be generally more compatible in biotite than in amphibole. Reported amphibole/melt partition coefficients of Ti in intermediate to felsic systems are usually in the range of 2–6, as compared to Dbiotite/melt of 17 in the present study. Nb and Ta are usually mildly incompatible in amphibole (Damphibole/melt of 0.2 to 0.8), while they are compatible in biotite. Only very limited data are available for typical compatible transition metal ions, but they also seem to indicate stronger partitioning into biotite than into amphibole. For V, Nandedkar et al. (2016) for example report a range of Damphibole/melt of 3.9 to 11.6, as compared to Dbiotite/melt of 35 in the present study. All these comparisons are, however, not entirely straightforward, as also the melt compositions in those studies were different.
The potential importance of allanite as a carrier of light rare earth in subduction zone lithologies was already pointed out by Hermann (2002), Klimm (2008), and Hermann and Rubatto (2009). These studies also contain some experimental data on allanite solubilities in silicate melts and on REE partitioning between allanite and melt. However, due to the much higher experimental pressures (> 20 kbar) and different bulk compositions of the melt, a comparison with the data from the present study is not straightforward. Hermann (2002) reported an allanite/melt partition coefficient of the light rare earth in the order of 200, which is at the lower end of the data obtained here. The difference is most likely related to the higher temperatures and pressures of those experiments, and maybe the lower silica content of the melts. Higher Ce and Nd partition coefficients, ranging from 538 to 2245 were reported by Klimm (2008). These authors also noted a very strong temperature dependence of allanite solubility, as observed in the current study. However, Klimm et al. (2008) argue that the “melt” phase in their experiments was actually a water-rich “supercritical” fluid, such that a direct comparison with the data presented here is not possible and indeed, the bulk solubilities of allanite reported by Klemm et al. (2008) appear to be significantly below those observed here.
The effect of biotite crystallization on the trace element abundances in granitic melts
Due to the generally incompatible behavior of the rare earths, biotite fractionation likely does not have a major effect on rare earth patterns, and in any case the effect of biotite fractionation would be subordinate as compared to the effect of amphibole. Moreover, in felsic magmas, the fractionation of rare earth elements is usually controlled by the solubility of accessory minerals, such as allanite, monazite and xenotime (e.g. Duc-Tin and Keppler 2015 and references therein). However, biotite strongly fractionates the transition metals and the high-field strength elements and here we argue that some of the characteristic abundance patterns of these elements in silicic magmas may be produced by biotite crystallization. Figure 7 illustrates the evolution of some element ratios in the residual melt with fractional crystallization of biotite, based on the biotite/melt partition coefficients reported in Table 2. Among the ratios shown in Fig. 7 a, Nb/Ta has received particular attention. This ratio is considerably lower in the continental crust and in nearly all accessible reservoirs than in chondrites. The chondritic Nb/Ta ratio is 19.9 (Münker et al. 2003), while the continental crust typically falls into the range of 8–14 (Rudnick et al. 2000; Münker et al. 2003; Tang et al. 2019). Most accessible mantle and oceanic crust reservoirs also have distinctly reduced Nb/Ta ratios. Various hypotheses have been discussed to explain the sub-chondritic Nb/Ta of most accessible terrestrial reservoirs, including a sub-chondritic bulk Earth composition, preferential partitioning of Nb into the core (Wade and Wood 2001), and a hidden mantle reservoir with super-chondritic Nb/Ta (Rudnick et al 2000). Most rock-forming minerals either do not incorporate significant amounts of Nb or Ta, or they prefer Ta over Nb, such that crystal fractionation would actually increase the Nb/Ta ratio of the residual melt. In particular, rutile fractionation usually has such an effect, although the relative fractionation of Nb and Ta between rutile and melt depends strongly on melt composition and temperature and may be reversed in some circumstances (Linnen and Keppler 1997; Schmidt et al. 2004; Xiong et al. 2011). Based on some experimental data and partition coefficients from coexisting phases in natural samples, Stepanov and Hermann (2013) proposed that biotite could be a mineral that prefers Nb over Ta and that could therefore reduce the Nb/Ta ratio of a melt by fractional crystallization or as a residual phase during melting. The data from the current study confirm this hypothesis. The ratio of DNb/DTa for biotite/melt partitioning observed here is about 2, very similar to the data compiled by Stepanov and Hermann (2013). However, the experimentally determined partition coefficients of that study are lower (0.16—1.96) than those observed here, possibly due to the higher pressure (25 kbar) in their experiments. Therefore, if one applied the high-pressure data of Stepanov and Hermann (2013) to fractionation processes in the crust, a very large amount of biotite fractionation would be required to significantly reduce Nb/Ta in the residual melt. In contrast to this, the partition coefficients obtained here imply that 15—30% of biotite fractionation are sufficient to reduce the Nb/Ta ratio of a melt from a chondritic value to the range found in the continental crust (Fig. 7b). It is therefore quite plausible that biotite fractionation could account for at least some of the reduction in Nb/Ta observed in upper crustal rocks. Indeed, Müntener et al. (2018) already noted a systematic decrease in the Nb/Ta ratio with increasing silica content in a compilation of global arc magma data and modelled this by fractional crystallization involving biotite. This mechanism, however, cannot account for the overall reduced Nb/Ta in most terrestrial silicate reservoirs, as this reduction is also seen for example in MORB samples (e.g. Münker et al. 2003), where biotite fractionation is impossible.
The strong partitioning of Ti into biotite (DTibiotite/melt = 17 ± 8) implies that already minor biotite fractionation will strongly deplete Ti in the residual melt. As proposed by Stepanov et al. (2014), this may effectively suppress the saturation of rutile, ilmenite, and similar Ti–rich phases, which all preferentially incorporate Ta as compared to Nb. Biotite fractionation (or the retention of biotite in the residue during partial melting) may therefore be an essential factor leading to Ta-enrichment in highly fractionated melts.
Biotite crystallization may play an important role in separating transition metals relevant to the formation of magmatic-hydrothermal ore deposits. Porphyry copper and molybdenum deposits are typically associated with intermediate to felsic magmas above subduction zones (e.g. Sillitoe 2010). While they represent enormous concentrations of Cu, Mo, and Au, other transition metals, in particular Zn are not strongly enriched. This cannot be due to fluid/melt partitioning, since Zn strongly fractionates into saline aqueous fluids (e.g. Holland 1972), just as Cu, Au, and to a lesser extent, Mo (e.g. Candela and Holland 1984; Keppler and Wyllie 1991; Frank et al. 2011). Zn appears to partition much less into sulfides than Cu (Li and Audetat 2012), such that any sulfide fractionation should actually enrich Zn over Cu in the residual melt. The efficient separation of Zn from Cu and Mo, therefore, requires a different mechanism and as illustrated in Fig. 7 a, biotite fractionation is an obvious possibility, as Zn is efficiently sequestered into biotite, while both Cu and Mo are incompatible. Indeed, an early study (Blaxland 1971) found a negative correlation of Zn contents in biotite with the modal abundance of this mineral, as one would expect if Zn is strongly fractionated into the earliest biotite crystallized. Biotite fractionation will also tend to mildly increase the Mo/W ratio, as Mo is incompatible in biotite, while W is more compatible (Fig. 7a).
Allanite stability in granitic systems
Unlike for biotite, allanite fractionation definitively would have a major effect on the trace element abundance in residual melts, as it strongly concentrates the light rare earths, with partition coefficients that may approach 103. Indeed, allanite appears to be the main carrier of light rare earths in metaluminous granites (Bea 1996). However, our experimental data also show that allanite is likely to crystallize early in granitic melts only if they are already unusually enriched in rare earth from the beginning. Otherwise, allanite is probably a phase produced during the late stages of cooling, as allanite solubility decreases strongly with temperature. The solubility is here expressed as the REE concentration in the melt in equilibrium with allanite. However, as allanite also incorporates Ca, Al, and Fe as essential constituents, the solubility likely also depends on the activity of CaO, Al2O3, and FeO in the melt. In particular, the FeO content in the starting glasses used here (Table S1) is with about 3.5 wt. % considerably higher than in most granites. If allanite solubility is described by some kind of solubility product of the constituent oxides, this would mean that in a typical granitic magma, the REE concentration in equilibrium with allanite should be even higher than that observed in our experiments. The experimentally observed light REE concentration in the melt is around 800 ppm at 800 ˚C and decreases to about 200 ppm at 750 ˚C. The upper end of this concentration range is considerably higher than the typical combined La, Ce, Pr, and Nd content in most granites. Total light REE concentrations near 1000 ppm are only known from a few highly enriched granites, while values below 100–200 ppm are more common (e.g. Ishihara et al. 2008; Li et al. 2017). Under most circumstances, allanite will therefore crystallize only late during cooling, when the solubility has dropped significantly. The importance of temperature in controlling allanite stability was already noted by Chesner and Ettlinger (1989) who observed allanite in units of the Toba tuff erupted below 800 ˚C, while it was absent above 800 ˚C.
Trace elements may enter biotite both in the 12-fold coordinated K site (heavy alkalis, alkaline earths, Pb, and light rare earths) as well as in the octahedral Mg site (most transition metals, heavy rare earths and high-field strength trace elements)
Biotite fractionation has a strong effect particularly on the transition metals. Biotite likely separates most first-series transition metals, including Zn, Co, Ni, and Ti from Cu and Mo, such that only the latter elements may ultimately form economic grade porphyry deposits.
About 15—30% of biotite fractionation could reduce the Nb/Ta ratio in felsic melts from a chondritic value to the range of values found in the continental crust. The strong partitioning of Ti into biotite may suppress the saturation in Ti-oxide phases and, therefore, facilitate the enrichment of Ta over Nb.
Allanite strongly concentrates the light REE, with partition coefficients in the 102–103 range. However, allanite solubility in the melt is strongly temperature dependent, such that it will likely form only in the last stages of cooling of a magma, except if the parental melt is unusually enriched in light rare earths.
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We would like to thank Thomas Wenzel (Tübingen) and Detlef Krauße and Anke Potzel (Bayreuth) for assistance in the microprobe analyses. Constructive reviews by two anonymous referees helped to improve the manuscript. This study was supported by DFG (German Research Foundation, Leibniz award to HK).
Open Access funding enabled and organized by Projekt DEAL.
Communicated by Othmar Müntener.
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Were, P., Keppler, H. Trace element fractionation between biotite, allanite, and granitic melt. Contrib Mineral Petrol 176, 74 (2021). https://doi.org/10.1007/s00410-021-01831-3
- Rare earths
- Nb/Ta ratio
- Porphyry copper deposits