Corresponding author: C. W. Thomas, Geological and Planetary Sciences, California Institute of Technology, 1200 E. California Blvd, MC 170-25, Pasadena, CA 91106, USA. (email@example.com)
 We performed 17 new shock wave experiments on preheated (1673 K) hedenbergite liquid (CaFeSi2O6) and two model basalt liquids (an equimolar binary mix of CaAl2Si2O8 + CaFeSi2O6 and an equimolar ternary mix of CaAl2Si2O8 + CaFeSi2O6 +CaMgSi2O6) in order to determine their equations of state (EOS). Ambient pressure density measurements on these and other Fe-bearing silicate liquids indicate that FeO has a partial molar volume that is highly dependent on composition, which leads to large errors in estimates of the densities of Fe-bearing liquids at ambient pressure based on an ideal mixing of any fixed set of end-member liquids. We formulated a series of mixing tests using the EOS determined in this study to examine whether ideal mixing of volumes might nevertheless suffice to describe the ternary system CaAl2Si2O8-CaFeSi2O6-CaMgSi2O6 at high temperature and pressure. The ideal mixing null hypothesis is rejected; compositional variations in partial molar volume of FeO appear to extend to high pressure. Only densities of Fe-bearing liquid mixtures with oxide mole fraction of FeO less than 0.06 can be adequately approximated using an ideal solution.
 Silicate liquids play a large role in our understanding of both the early and modern Earth. Most widely accepted scenarios for the evolution of the early Earth involve at least one stage of extensive or complete melting, for example in the aftermath of impacts with large proto-planetary-sized objects such as the presumed moon-forming event[Canup, 2004, 2012; Canup and Asphaug, 2001; Ćuk and Stewart, 2012]. The chemical and thermal evolution of the early molten mantle and how it affects the chemistry and physical properties of the modern mantle are not well understood. Furthermore, seismic observations of the 410 km discontinuity in the upper mantle [Revenaugh and Sipkin, 1994; Song et al., 2004] and ultralow velocity zones in the lowermost mantle [Garnero and Helmberger, 1995; Williams and Garnero, 1996] have been interpreted to indicate the presence of a neutrally buoyant partial melt, yet there is currently limited knowledge of how the density and compressibility of complex silicate liquids behave at high temperature and pressure. It is therefore essential to have experimental constraints on the equation of state (EOS) of the complex multicomponent silicate liquids that would be actually present in nature. The difficulty lies in that natural silicate liquids comprise a potentially infinite, multidimensional continuum of compositions. Understanding their range of volumetric behavior requires either data on an arbitrarily large number of experiments or data on a minimum set of end-member compositions along with a reliable tool of interpolating among them. Choosing the correct method of interpolation is key to producing a predictive model for silicate liquid density and compressibility over a wide range of pressure, temperature, and composition space. Experimental data that provide constraints on end-member volumes as well as a few intermediate compositions offer the opportunity to test whether available methods for such intepolation are reliable.
 Ideal mixing of volumes has proven to be a reliable method of interpolation for ambient pressure experiments within a given compositition and temperature range [Bottinga and Weill, 1970; Bottinga et al., 1982; Bottinga et al., 1983; Guo et al., 2013; Lange, 1997; Lange and Carmichael, 1990; Mo et al., 1982; Nelson and Carmichael, 1979], although exceptions from ideality exist and are discussed below. Likewise, ideal mixing silicate liquid volumes at high pressure has been employed as a simplifying assumption, but it in fact remains poorly tested and constrained [Asimow and Ahrens, 2010]. In this study, we report 17 new shock wave experiments to pressures up to 146 GPa on preheated silicate liquids of three separate compositions: hedenbergite (Hd; CaFeSi2O6), a 50–50 mixture of anorthite and hedenbergite (An-Hd; CaAl2Si2O8-CaFeSi2O6), and an equal mixture of anorthite, hedenbergite, and diopside (An-Hd-Di; CaAl2Si2O8-CaFeSi2O6-CaMgSi2O6). Determination of the EOS of Hd and the two mixtures (or “model basalts”) permits us to test the validity of linear mixing of volumes and ideal configurational mixing of entropies — two assumptions which were both used in Thomas et al.  and Thomas  to predict the volumes of multicomponent liquids at high T and P.
2.1 Sample Preparation
 The synthesis and analysis for the Hd and model basalt samples used in this study are described in Guo et al.  and Guo , respectively. These studies also describe the 1-bar double-bob Archimedean density measurements and the ultrasonic sound speed measurements that were completed on these materials. The sample materials used for the shock wave experiments were cored directly from the lower buffer rod crucible used in the sound speed determinations. The cores were sliced into disks, which were then lapped down to under-fill the volume of the molybdenum shock-experiment sample holder. The Mo sample holders are assembled from two machined pieces: (1) the driver plate, which has a hollow cylindrical projection on one side that becomes the sample well and (2) the cap, which is a 1 mm thick, 8 mm diameter disk that is welded on after filling (for complete description of the welding process see Thomas et al. ). The interior volume of the sample well is 8 mm in diameter and 2.5 mm deep. The samples under-filled this volume by 7–13% at room temperature to prevent the welded cap from bowing during heating [c.f. Thomas et al., 2012]
 The surfaces within the sample well including the inside surface of the cap were polished to a mirror finish with 1 micron alumina grit. Smoothing all the surfaces prevents bubbles from clinging to the walls of the sample holder during heating and potentially interfering with the imaged shock wave. The outer surface of the cap was left with the finish quality as-machined (~9 micron finish), in order to match the quality of polish on the inner portion of the rear face of the driver plate, which was polished on a rotating stage. The speed of the polishing pad decreases towards the center; hence, the quality of mirror finish also decreases. Approximately, similar finishes on the cap and driver reflecting surfaces ease acquisition of evenly illuminated images of the cap and driver during the shot and greatly increased the precision of the Hd data given below. On the contrary, the model basalt capsules were polished as in the manner as described in Thomas et al.  due to the larger quantity of light needed for the digital recording system [c.f. Thomas, 2013] (see Chapter 3). Hence, this data set is plagued with larger errors derived from determining the driver and cap arrivals with different exposure levels. Additional sample preparations are detailed in Asimow and Ahrens , and Thomas et al. .
2.2 Experimental Setup
 The pioneering work for shock studies on molten materials is Rigden et al. . The description of our methods below builds on this and the work of Rigden et al. [1988, 1989], Miller et al. [1988, 1991], Chen and Ahrens , and Chen et al. . The most recent changes to experimental techniques and data analysis are in Asimow et al. , Asimow and Ahrens , and Thomas et al. .
 For this study, 17, total experiments were performed—12 in the Caltech 90/25 mm two-stage light gas gun and five using the Caltech 40-mm propellant gun—eight performed on Hd, five performed on An-Hd, and four performed on An-Hd-Di (see Table 1). All shots were preheated to 1673 K ± 4 K (1400°C) and used either molybdenum (Mo), tantalum (Ta), or aluminum alloy (Al2024) flyer plates. Flyer plate velocities (ufp) ranged from 1.46 to 6.19 km/s; the methods used for measuring ufp are given in Chapter 3 of Thomas 
 During each experiment, the rear face of the target is illuminated by a Specialized Imaging xenon spark lamp and filmed by a Hadland Imacon 790 streak camera through a narrow (25 µm) slit focused horizontally across the center of the driver and sample cap. Hd shots were recorded on Polaroid film; the model basalts were recorded using a digital system [c.f. Thomas, 2013]. As the shock wave reaches the free surface of the driver or the cap, the reflected light from the polished surface is extinguished (or shows a sharp change in intensity). The offset time of these two cutoffs allows for the precise measurement of the shock transit time through the sample and molybdenum cap.
 To correct for nonuniform streaking rate, the camera was calibrated using a test streak image modulated by a radio-frequency tuner at 148.9875 MHz for a 1500 ns streak length and by a pulse generator at 1.7870 MHz for a 5000 ns streak (shot 1068). Each pixel line on the shot streak record can then be converted to a time during the experiment, which permits the shock transit time through the sample to be calculated from the pixel distance between the two cutoffs on the film (or digital image). A detailed method for picking cutoffs and reducing the data is described in Thomas et al. .
 The final calculated shock state — i.e., shock pressure (PH), shock density (ρH), particle velocity (up), and shock velocity (Us) — is solved for iteratively [Rigden et al., 1988] using measured shock wave travel time, impedance matching, the Rankine-Hugoniot equations, Hugoniot data (ρo, Co, and s) for the metal flyer plates and hot Mo driver (Table 2), and the initial density (ρo) for each of the silicate liquids (see Tables 3, 4, and 5). An initial guess for the bulk sound speed (Co) and Hugoniot slope s is required to seed the iteration, but the converged result is independent of this assumption. Uncertainties in all derived parameters (Us, up, PH, and ρH) were obtained from the uncertainties in the measured and standard parameters by analytical error propagation [c.f. I Jackson and Ahrens, 1979].
Table 3. Equation of State Fits for Molten CaFeSi2O6a
SWEOS= shock wave equation of state. 3BM/MG = third-order Birch-Murnaghan/Mie-Grüneisen EOS 4BM/MG = fourth-order Birch-Murnaghan/Mie-Grüneisen EOS Sources: Fitted indicates an adjustable parameter, L97 is Lange , LN92 is Lange and Navrotsky , G13a is Guo et al. .
 The shock wave data are reported in Table 1, including shot number, flyer material, the temperature prior to firing, ufp, up, US,ρH, and PH.
 A Hugoniot is a series of peak shock states achieved by progressively stronger shocks in a material from the same initial condition [Ahrens, 1987]. The Hugoniot of a well-behaved material empirically forms a line in US-up space, given to third order in strain by US = Co + s up [Jeanloz, 1989]. The bulk sound speed of the material at room pressure, Co, is given by the intercept; the slope (s) is related to K′S, the isentropic pressure derivative of the isentropic bulk modulus (KoS) by [Ruoff, 1967],
3.1 Hedenbergite (CaFeSi2O6) Liquid
 Figure 1 shows linear fits to the Hd shock data in US-up space. An unweighted linear fit to all eight preheated hedenbergite liquid data points yields US = 2.587±0.142 + 1.55±0.04 up km/s (r2 = 0.996). The experimentally determined ultrasonic value of the bulk sound speed, 2.613±0.016 km/s [Guo et al., 2013], lies within the stated uncertainty of the bulk sound speed derived from the intercept of this fit, 2.587±0.142 km/s. This relationship indicates relaxed (liquid-like) — as opposed to un-relaxed (glass-like) — behavior upon shock compression [Rigden et al., 1988]. Therefore, to reduce the error on the linear fit, we fixed the intercept at the mean ultrasonic value yielding an unweighted constrained linear fit of US = 2.613 ± 0.016 + 1.54 ± 0.01 up km/s (r2 = 0.999).
 It is necessary to select and apply a thermal equation of state formalism for investigating material properties that lie off the Hugoniot, since the Hugoniot achieves temperatures and energies much higher than those of geophysical interest at lower mantle pressures (even for processes during early Earth differentiation). We have defined the entire P-V-E surface of hedenbergite liquid using various formalisms: the shock wave equation of state (SWEOS) and the third- and fourth-order Birch-Murnaghan Mie-Grüneisen EOS (3BM/MG and 4BM/MG). For a full description of the thermal EOS equations and fitting procedures, the reader is directed to Asimow and Ahrens  and Thomas et al. . The results and uncertainties for each fit on Hd are given in Table 3, and the Hugoniots are plotted in Figure 2.
 The SWEOS is defined by a linear Hugoniot in US-up space, converted to P - ρ space using the first and second Rankine-Hugoniot equations [e.g., Ahrens, 1987]. States that lie off the Hugoniot are found using the Mie-Grüneisen thermal pressure approximation with a temperature-independent power law expression for the thermodynamic Grüneisen parameter
 Although a value for q to be used with the SWEOS was not independently determined in this study, experimental results thus far indicate that silicate liquids—including iron-bearing liquids [Thomas et al., 2012]—appear to have q values of −0.88 to −2 for compressions of 1 > ρo/ρ > 0.49. The slope and intercept of the constrained Hugoniot fit given above correspond to a K′S value of 5.16±0.04 derived from (1) and a KoS value of 19.98±0.24 GPa derived from the expression
 The third- or fourth-order BM/MG EOS is defined by a third- or fourth-order Birch-Murnaghan isentrope centered at 1 bar and 1673 K and a Mie-Grüneisen thermal pressure approximation. The 3BM/MG fit result is KS′ = 6.22±0.55, q = −1.93±0.41, and reduced χ2= 4.20. The 4BM/MG fit result is KS′ = 3.15±1.67, KS″ = 0.78±0.60 GPa−1, q = 0.47±9.86 and reduced χ2 = 3.26. The high precision for most of the points in the Hd data set propagates into unusually high χ2 values for both fits. Nevertheless, comparatively, the 4BM/MG has very large error bars on and strong correlations among the output parameters indicating a very unstable fitting routine. The 3BM/MG fit, by contrast, has less severe correlation between the parameters and appears justified by the fitting statistics. Hence for this data set, we prefer the third-order fit.
3.2 An-Hd Liquid
 The An-Hd Hugoniot in US-up space is shown in Figure 3. The unweighted linear fit is US = 2.742±0.282 + 1.40±0.09 up km/s (r2 = 0.986). As observed above for Hd liquid, the An-Hd liquid appears to be relaxed upon compression as the experimentally determined bulk sound speed, 2.772±0.011 km/s [Guo et al., 2013], and the intercept are within error. We can then fix the intercept at the mean ultrasonic value yielding an unweighted constrained linear fit of US = 2.772±0.011 + 1.39±0.03 up km/s (r2 = 0.998). This slope and intercept constrain the SWEOS K′S and KoS values to be 4.54±0.12 and 21.30±0.25 GPa, respectively.
 The 3BM/MG fit result is KS′ = 5.49±0.65, q = −0.18±2.25, and reduced χ2 = 6.37. The 4BM/MG fit result is KS′ = 5.10±1.61, KS″ = −0.17±0.60 GPa−1, q = 1.67±2.79 and reduced χ2 = 12.53. Both fits have relatively large error bars and large reduced χ2 due to the low number of data points and fairly significant scatter in P-ρ space (Figure 4). Yet both fits give similar K′S to SWEOS, which is well defined by the linear fit. We therefore prefer the third-order fit despite having large errors, since it fits the data sufficiently well, has a lower reduced χ2, and exhibits a negative q value, which has been shown to be typical for silicate liquids[Thomas, 2013].The EOS parameters and their uncertainties for An-Hd liquid are given in Table 4.
3.3 An-Hd-Di Liquid
 The An-Hd-Di Hugoniot in US-up space is shown in Figure 5. The unweighted linear fit is US = 2.823±0.197 + 1.52±0.09 up km/s (r2 = 0.995). Behaving as the two liquids above, An-Hd-Di liquid is relaxed upon compression [Guo, 2013], which justifies an unweighted constrained linear fit of US = 2.846±0.014 + 1.54±0.02 up km/s (r2 = 0.999). This slope and intercept constrain the SWEOS K′S and KoS values to be 5.15±0.06 and 22.03±0.25 GPa, respectively.
 The An-Hd-Di liquid was fit only with the 3BM/MG, as fitting the 4BM/MG to so few data points is under-constrained and does not yield a meaningful reduced χ2. The 3BM/MG result is KS′ = 6.20±0.17, q = −1.14±0.79, and reduced χ2 = 0.39. The results and uncertainties for each fit on An-Hd-Di are given in Table 5, and the Hugoniots are plotted in Figure 6.
4.1 Linear Mixing Assumptions
 To make progress on calculating the volumetric properties of the natural multicomponent silicate liquids that may occur in the lower mantle, the plan has been to constrain the EOS for a number of important end-member liquids using shock wave studies and then to attempt to reliably interpolate among them. End-member liquids that have been determined previously using shock wave methods are: Fe2SiO4 (Fa, fayalite), Mg2SiO4 (Fo, forsterite), MgSiO3 (En, enstatite), CaAl2Si2O8 (An, anorthite), and CaMgSi2O6 (Di, diopside). The recommended EOS parameters for each of these end-members are given in Chapter 3 of Thomas . In Thomas et al. , these five end-members were used to interpolate within the CaO-MgO-Al2O3-SiO2-FeO major element component space to constrain the volume of a liquid along an isentropic temperature-pressure path for a desired composition, yet there was not a clear test of the validity of the two underlying assumptions: (1) linear mixing of volumes and (2) constant entropy of mixing for a given composition.
 The assumption of linear or ideal mixing is simplest assumption that can be made for mixtures,
where the volume of mixing (Vmix) is assumed to be zero, and hence the total volume (Vtot) is just a linear combination of the end-member partial molar volumes (V i) multiplied by their respective mole fractions (Xi). The second assumption is that the configurational entropy of a liquid solution is a function of composition only and therefore does not change with variations in temperature and pressure for a chosen liquid composition, such that
where the entropy of mixing (Smix) is assumed to be a constant value for each composition and hence an isentrope or constant entropy path in T-P space can be found from
where the T and P derivatives of entropy come from standard thermodynamic identities. Our data do not provide a test of this method of computing isentropes, since we lack experimentally defined isentropes for reference. Assuming configurational entropy to be function of composition only cannot be explicitly true if cation speciation is changing; hence, this serves only as our best approximation. We therefore focus on evaluating the volume of mixing assumption by comparing isentropes for intermediate compositions constructed with different sets of end-members, while acknowledging that this exercise may be compromised to some extent by the configurational entropy issue.
4.2 Glass and 1 Bar Melt Data
 Both of these assumptions given in the section above have historically performed fairly well at 1 bar. Linear mixing of temperature-independent partial molar heat capacities has been a successful model for most silicate liquids [Stebbins et al., 1984]. Similarly, linear mixing of volumes has been successful in determining silicate liquid densities in most major element space (SiO2-Al2O3-MgO-CaO-Na2O-K2O) [Lange, 1997; Lange and Carmichael, 1990]. However, exceptions to both rules do exist. Heat capacities for the Fe2O3 oxide component were shown to vary strongly with composition [Lange and Navrotsky, 1992], and the partial molar volumes of Fe2O3 and TiO2 components are both variable with composition. These exceptions are attributed to the Fe3+ and Ti4+ cations having multiple coordination states at ambient pressure that are highly dependent on the composition, i.e., fraction of non-SiO2 components [Liu and Lange, 2001, 2006].
 More recent results have found this to be potentially true for Fe2+ as well, in that the partial molar volume of FeO (VFeO) in a melt is observed to depend on composition in some cases [Guo et al., 2013]. Such behavior of Fe2+ is well documented in the glass literature, which is important insofar as glasses provide a proxy for structural properties of melt at the glass transition temperature. When discussing melt structure, language is typically borrowed from random network theory [Zachariasen, 1932], which distinguishes oxides as network formers, network modifiers, or intermediates. Network-forming cations (e.g., Si4+) occur typically in tetrahedral () oxygen coordination in various connected units in the melt, whereas network modifiers (e.g., CaO, MgO) typically occupy octahedrally () coordinated sites and disrupt the tetrahedral network. Intermediates (e.g., Al2O3, TiO2) can take on either role, may occupy multiple coordination sites, and may either disrupt or stabilize the polymerization of a melt [Bottinga and Weill, 1972; Mysen, 1983, 1988]. This is a simplified view of glasses and melts, but it acts to guide our intuition concerning the behavior of cations and the contributions of Fe3+ and Ti4+ to the density, heat capacity, and other thermodynamic properties of silicate melts [Burns, 1993; Mysen, 1988].
 FeO is an intermediate glass former and has been documented to take on a range of  to  coordination dependent on composition. Fe2+ is predominantly a network modifier in basaltic glasses [Burns, 1993; W E Jackson et al., 2005; Mysen, 1983, 1988] and also likely in melts with similar SiO2 mole fraction. This is supported by the relatively low 1 bar VFeO value (~12.1 cm3/mol) for An-Hd, An-Di-Hd, and Hd-Di model basalts at 1732 K. This VFeO has been inferred to indicate an average Fe2+ coordination of ~[5.7] due to its similarity to the molar volume of wüstite, crystalline FeO (in which Fe2+ is octahedrally coordinated) [Guo et al., 2013]. On the contrary, Fe2SiO4 glasses contain very low-coordinated Fe2+ and are surprisingly polymerized [Cooney and Sharma, 1990]. X-ray absorption spectroscopy studies of both glass and melt of fayalite composition infer an average coordination of ~ [W E Jackson et al., 1993]. This is again supported by melt densities, where VFeO increases to ~14–17 cm3/mol [Mo et al., 1982; Shiraishi et al., 1978; Thomas et al., 2012], similar to the molar volume of crystalline CaFeO2, a structure in which Fe2+ is  coordinated [Guo et al., 2013].
 Between these two extremes, Hd and the CaO-FeO-SiO2 (CFS) melts measured in Guo et al.  display FeO in an average coordination state intermediate between  and . The VFeO for Hd melt (~15.47 cm3/mol) is inferred to indicate [4.7] coordination, similar to the values in Hd glasses (~4.3) and in molecular dynamics simulation of this melt [Rossano et al., 2000]. The inferred coordination for CFS glasses range from 4.6 to 5.2. Guo et al.  present an inverse correlation between CaO concentration and average Fe2+ coordination number. This is contrary to expectation from the model in Jackson et al.  based on valence bond (VB) theory, which suggests a direct correlation between the concentration of network modifying cations (those with higher bond valence with oxygen than Fe, i.e., Ca, Mg, Na, and Rb) and FeO coordination. For example in the VB model, Ca would have a greater “share” of the O valence due to the higher bond valence of the Ca-O bond and force Fe to find charge balance with other oxygens and hence increase coordination at a fixed Si content.
 Hence, the composition dependence of Fe coordination in CFS melts appears to be also strongly related to the degree of polymerization (Si/O ratio) [Burns, 1993] due the intermediate nature of Fe. For example in Hd, where SiO2 is high (Si/O =0.33) and there are equal proportions of CaO and FeO, FeO fills both roles of network former and modifier with an average value of [4.7]. For the family of CFS melts studies by Guo et al. , the Fe content is fixed (40 mol %) and so increasing CaO is coupled to decreasing SiO2; therefore, the Fe2+ may be energetically forced to play the role of network former as CaO competes more effectively for octahedral sites. This competition would effectively lower the average Fe coordination, opposite of the effect predicted by the VB model. Qualitatively, one can understand the importance of FeO as an intermediate behavior cation when Fe2SiO4 is compared to Mg2SiO4 melt, which has the same low Si/O ratio (0.25). Since MgO acts only as network modifier and cannot act as a network former, Mg-rich melts typically have fully depolymerized structure and display very low viscosities [Urbain et al., 1982]. For fayalite liquid, FeO is energetically favored as a network former to accommodate the charge balance of the oxygen, creating a highly polymerized glass as observed by Cooney and Sharma .
 The dependence of FeO coordination and molar volume on other cation concentration invalidates the assumption of linear mixing of volumes at 1 bar for FeO-bearing liquids. It is unclear, however, what effect pressure and temperature may have. For glasses, higher temperatures are believed to decrease the coordination of transition metals [W E Jackson et al., 2005], and there is some evidence that cations in melts will favor a coordination state lower than that of the glass [W E Jackson et al., 1993]. At low pressure, network forming SiO4 tetrahedra predominate, but as P increases, Si4+ coordination increases (~6.5 at 150 GPa) [Karki et al., 2007]. Less is known about the coordination of network modifiers at high pressure. Preliminary modeling of Fe2SiO4 liquid shows decreasing Fe-O bond length and increasing coordination of Fe with pressure, but this does not constrain the effect of other cations [D. Muñoz Ramo and L. Stixrude, Spin crossover in Fe2SiO4 liquid at high pressure, submitted to Physical Review Letters, 2013]. Guo et al.  provides indirect evidence that coordination of Fe2+ in basaltic melts may decrease towards  at moderate pressures (~5 GPa).
 The only previous test of linear mixing at high pressure and temperature was for Fe-free anorthite-diopside liquids [Asimow and Ahrens, 2010], which found the linear approximation suitable at elevated T-P conditions along the measured Hugoniots. Linear mixing appeared to fail at low temperatures, but this may have been an artifact of uncertainties in the large extrapolation downwards from the Hugoniot temperature. Another partial success for linear mixing was found in MD simulations of An-Di and also in MD simulations of the MgO-SiO2 binary, each of which showed well-behaved mixing at high pressure which began to break down at lower pressure [de Koker et al., 2013; Martin et al., 2012].
4.3 Tests of Linear Mixing
 Our first test examines whether the VFeO difference between Fe2SiO4 and CaFeSi2O6 at 1 bar is still significant at high temperature and pressure. That is, can VFeO for either end-member substitute for the other, as it would in the case of ideal mixing of volumes? To test this, we compare the Hd isentrope from shock wave experiments determined in this study to a modeled linear combination of end-member liquids, where HdmodelFa = Di + 0.5 Fa – 0.5 Fo. The equations and details of creating isentropes of mixtures are given in Thomas et al. . The results are shown in Figure 7, where it is apparent that the model does not capture the behavior of the Hd isentrope. The errors for temperature and density are highly correlated such that if the model predicts a lower temperature than the actual isentrope, it will over predict the density and vice versa. Such is the case for Hd, where the errors at high pressure (~120 GPa) and temperature are maximized, and the model underestimates the temperature by 30% and overestimates the density by 20% (Figure 7b). A successful model for linear mixing would have errors for density of 1–2%, which is the average experimental error for a shock wave experiment. In this test, comparing the use of two Fe-rich end-members, we find a failure of linear mixing, and this is presumably due to complexity in the coordination state of Fe2+.
 Our second test examines the question: Which model will perform better in creating an Fe-rich model basalt, An-Hd — using VFeO derived from Fa or VFeO derived from Hd? Our expectation from 1 bar coordination numbers is that Hd should be a better end-member for modeling An-Hd. Two mixing models, AnHdmodelFa = 0.5 An + 0.25 Fa – 0.25 Fo + 0.5 Di and AnHdmodelHd = 0.5 An + 0.5 Hd, are compared to the An-Hd isentrope determined in this study. It can be seen in Figure 8 that neither model is able to recover the An-Hd isentrope, but that the Fa model does significantly worse. The Fa model also becomes unphysical at high pressure and lower temperature (Figure 8a), and this breaks the anticorrelation between errors in T and ρ, which are both underestimated, by 15% and 10% at 120 GPa, respectively (Figure 8b). The Hd model does significantly better with maximum errors at 120 GPa that overestimate T by 6% and underestimate ρ by 7% (Figure 8d). These errors worsen systematically for isentropes with progressively higher potential temperature (Figure 8c). These results are in line with our expectations based on 1 bar results: neither Fa nor Hd model can fully recover the behavior of the An-Hd isentrope, but closer similarity of VFeO at 1 bar for Hd and An-Hd is significant enough to improve the fit at high pressure and temperature.
 Our third test examines the question: As FeO content decreases, does the difference between the end-member VFeO and that of the model basalt still play as significant of a role in the final volume of the mixture at high pressure and temperature? We attempt to recover the isentrope of the model basalt, An-Hd-Di (which has less FeO than the previous An-Hd basalt), again using Fa and Hd end-member models: AnHdDimodelFa = 0.33 An + 0.667 Di + 0.167 Fa – 0.167 Fo and AnHdDimodelHd = 0.33 An + 0.33 Hd + 0.33 Di. The results in Figure 9 show improvement for both models with the Fa model having high-pressure errors that underestimate T by 12% and underestimate ρ by 4% and the Hd model overestimating T by only 3% and underestimating ρ by 3%. Again, the Hd model does significantly better than the Fa model, likely due to the greater structural similarity of FeO in Hd and in An-Hd-Di at 1 bar. This test also suggests, at least in the studied region of CaO-FeO-MgO-Al2O3-SiO2, that the linear mixing approximation becomes better as the amount of FeO in the mixture decreases. That is, despite the variable behavior of VFeO, there may be a threshold concentration of FeO below which this is negligible and the ideal solution approximation is adequate.
 We have chosen to perform these tests along isentropic paths since the corresponding temperature regimes are more geologically relevant than the very high temperatures along a Hugoniot. Yet these same three tests can be performed along the Hugoniot of a liquid [c.f. Asimow and Ahrens, 2010] or any other chosen P-T path.
 To show this, Figure 10 presents these tests performed along the calculated P-T path for the intermediate liquid Hugoniots of Hd, An-Hd, and An-Hd-Di (Figures 10a, 10b, and 10c, respectively). Each diamond point corresponds to the EOS fit of an experimental point, and the error bars represent the average experimental error for that data set. A successful linear mixing model would reproduce the density within this given experimental error. Since each end-member Hugoniot (Fa, Fo, An, Di, and Hd) lies on its own separate P-T path, a Mie-Grüneisen approximation is used to adjust the temperature to of that of the given intermediate Hugoniot. This variable thermal pressure correction adds greater complexity in quantifying the error due to the temperature estimation, yet emphasizes that linear mixing of volumes is dependent on the chosen P-T path as was shown previously for Fe-free liquids [Asimow and Ahrens, 2010]. This dependence can be seen in Figure 10a, which displays the density of Hd underestimated at all pressures along the Hugoniot whereas it was previously overestimated along the isentropic path (Figure 7). What is still captured though is the inability of the HdModelFa to match the slope of the Hd Hugoniot as it was also unable to match the slope of the Hd isentrope (Figure 7). Likewise, mixing tests for An-Hd and An-Hd-Di Hugoniots (Figures 10b and 10c) give qualitatively similar results to their isentropic equivalent tests (Figures 8 and 9) in that there is an improvement in the linear mixing model as FeO content is decreased. In fact, the An-Hd-Di Hugoniot can be approximated within the average experimental error (1.9%) using the linear combination of An, Hd, and Di volumes. Thus, as is true for the isentrope, it appears that an Fe-bearing end-member close in composition to the intermediate liquid of interest is needed for adequately predicting temperature and density along the Hugoniot.
 It still remains to define the best choice for VFeO (i.e., Fe2+ coordination state) for modeling a particular liquid composition in the mantle and to define the threshold FeO concentration below which this choice is unimportant. Our final test attempts to answer these questions by comparing the original chondrite model isentrope given in Thomas et al.  that uses Fa as the VFeO component (ChmodelFa= 0.62 En + 0.24 Fo + 0.08 Fa + 0.04 An + 0.02 Di), and a model which uses An-Hd-Di as the VFeO component (ChmodelAnHdDi = 0.62 En + 0.32 Fo + 0.45 AnHdDi – 0.12 An − 0.28 Di). We again focus on isentropic P-T paths as they are most geologically relevant. The results in Figure 11 show that the An-Hd-Di model predicts a slightly higher temperature but that models are within ±1.5% for both T and ρ. Hence, the models are effectively indistinguishable, indicating that liquids with XFeO ≤ 0.06 (chondrite model [Andrault et al., 2011]) can be suitably approximated with linear mixing. Mole fractions greater than this amount, such as An-Hd-Di (XFeO = 0.08), can be approximated within reasonable error (±3%), but only when using an FeO component that has a similar VFeO at 1 bar.
 Direct knowledge of the coordination state of Fe2+ in a given liquid thus is an important constraint on the volume behavior of that liquid, especially for high FeO contents. Conversely, precise data on the equation of state of an Fe-bearing liquid can be interpreted primarily as a constraint on the coordination state of Fe2+ in that liquid. However, liquids containing Fe2O3, Na2O, K2O, varying amounts of SiO2, and other oxide species are far more complex than the five-component system studied so far. Other cations may influence the Fe2+ coordination state and may have variable coordination states themselves. In situ experiments analyzing cation coordination of complex glasses and melts at high pressure and temperature would greatly aid in elucidating these consequences and complementing macroscopic constraints from shock wave or other equation of state measurements.
 We completed 17 new preheated shock wave experiments on Hd, An-Hd, and An-Hd-Di liquids to determine the EOS of each composition. Having data on more compositions than are necessary to span the multicomponent oxide system, we applied these data to testing the validity of ideal mixing of volumes as a method of interpolation among end-member liquids. Ambient pressure density measurements on these and other Fe-bearing silicate liquids indicate that FeO has a molar volume (and therefore coordination state) that is highly dependent on composition [Guo et al., 2013], and our results show that this behavior extends to high pressure. An Fe-bearing end-member close in composition to the liquid of interest is necessary for adequately predicting temperature and density along its isentrope or Hugoniot. We find that deviations from linear mixing of volumes are significant at the level of several percent for liquid mixtures with molar XFeO >0.06 and are also dependent on the chosen P-T path; therefore, caution should be taken when attempting to calculate densities of Fe-bearing liquids, being attentive to Fe content and P-T conditions. On the other hand, densities and isentropic gradients for liquids in the system CaO-FeO-MgO-Al2O3-SiO2 with less than this threshold concentration of FeO can be approximated both at ambient and at high pressure using ideal volume of mixing.
 The authors would like to thank the following: the shock wave lab technical staff—Oleg Fat'yanov, Eprapodito Gelle, Russel Oliver, and Emma Dodd. Thanks to X. Guo and R. A. Lange for their ongoing collaboration and willingness to share their manuscripts. This work was supported by the National Science Foundation through award EAR-1119522.