• Tidak ada hasil yang ditemukan

1. Experimental Investigation of Hydrous Melting of the Earth’s Upper Mantle, and 2. Olivine Abundances and Compositions in Hawaiian Lavas

N/A
N/A
Protected

Academic year: 2023

Membagikan "1. Experimental Investigation of Hydrous Melting of the Earth’s Upper Mantle, and 2. Olivine Abundances and Compositions in Hawaiian Lavas"

Copied!
266
0
0

Teks penuh

In particular, I must acknowledge the contributions of Andrew Matzen, Laura Hebert, Sarah Miller, June Wicks, Ryan Petterson, Kevin Lewis, Ravi Kanda, Bob Kopp, and Charlie Verdel from that population for their help and. Finally, I must acknowledge and thank my wife, Jennifer Balta, for putting up with years of me coming home in a bad mood late at night after an experiment failed or after a long rehearsal, for always being there for me, for listening always. even when I didn't want to talk, because I was my best friend and that I was everything I could ask for in a partner.

Experimental investigation of hydrous melting of the Earth’s upper mantle It is now well established that volatile elements including carbon and water strongly

The hydrous melt experiments also show important changes in the composition of the coexisting clinopyroxenes. Clinopyroxene aluminum content has been suggested to be particularly important for the partitioning of a number of elements during melting due to coupled substitutions between trace elements and aluminum in the clinopyroxene structure (e.g. Blundy et al., 1998).

Olivine abundances and compositions in Hawaiian lavas

INTRODUCTION

Other solutions have been proposed to resolve this controversy, such as melting of different pyroxenites in the MORB source (Hirschmann and Stolper, 1996), elevated melting pressure (Shen and Forsyth, 1995), or increased compatibility of rare earth elements in aluminous clinopyroxene (cpx) at high pressures (Blundy et al., 1998). Second, we show that the presence of carbon, even at low concentrations, interacts with water in the fluid and can serve to counteract some of the effect of the presence of water.

METHODS

  • General approach
  • Analytical techniques

This improves the multiple saturation technique by making the solid compositions more representative of the mantle. Water content was calculated from absorbances based on the composition-dependent calibration of Ohlhorst et al. 2001) and electron probe analyzes of the major element glass composition.

RESULTS 1. Recrystallization experiments

  • Hydrous melting experiments

These two samples would require a loss of less than 10% of the available Fe in the fluid to the capsule to be consistent with other measured KD values. The iron content was variable between successive experiments due to the initial state of the liquid and the capsule.

DISCUSSION

  • MgO, FeO, SiO 2
  • TiO 2
  • H 2 O contents and implications for mantle melting and partitioning Our experiments are typically more hydrous than the liquids that might be
  • Additional implications of these experiments for natural melting

In the higher FeO experiments, the MgO content of the liquid was brought to a lower value by crystallization of solids. This behavior is consistent with the compositions of the cpx grains measured in the anhydrous melting experiments discussed here.

CONCLUSION

Since anhydrous melt is expected to be produced at higher pressures than anhydrous melt, these two effects will interact and potentially create very complicated relationships between liquid and solid Na2O content, pressure and composition. Hydrous melting of especially pyroxenite lithologies can be expected to show elevated Na2O if the effects of water on cpx are similar to those seen in peridotite, in the opposite direction of the simple relationship between K2O/Na2O and pressure. Therefore, the presence of water can be expected to increase the potassium content of erupted fluids at mid-ocean ridges by increasing the volume of peridotite melting.

Alternatively, K2O and water content in enriched sources would be expected together (Asimow et al., 2004). Elevated potassium in fluids can be expected to show interesting correlations with other indicators of source enrichment, and isolating any of these effects in natural MORB may require detailed modeling. The presence of water during melting at 3GPa produces fluids with increased SiO2 content and decreased (MgO+FeO)/SiO2 ratio compared to anhydrous melts at the same pressure, which is consistent with the results of hydrous melting experiments at lower pressures.

ACKNOWLEDGEMENTS

A modified iterative sandwich method for the determination of near-solidus partial melt compositions. 2009) Dehydration melts of nominally anhydrous mantle: the primacy of partitioning. 1996) Water in the oceanic upper mantle: implications for rheology, melt extraction and the evolution of the lithosphere. 1997). 1968) Compositions of magmas formed by partial melting of the Earth's upper mantle. 1969) System forsterite-diopside-silica with and without water at high pressure. The concentration, behavior and storage of H2O in the suboceanic upper mantle: implications for mantle metasomatics.

The hafnium paradox and the role of garnet in the source of mid-ocean ridge basalts. 1999). The role of clinopyroxene in the generation of U series disequilibrium during mantle melting. 2007) High-pressure partial melting of gabbro and its role in the Hawaiian magma source. Values ​​in parentheses are 100 * the standard deviation of the electron microprobe analyses, except in the modal abundance column, which is calculated.

Table 2: experimental results
Table 2: experimental results

ANALYTICAL TECHNIQUES

Additional analyzes were performed for this study to better constrain the MnO content of the phases. All analyzes were performed using a Caltech JEOL JXA-8200 electron microprobe in wavelength dispersion mode. Initial research measurements of the solid phases were performed with counting times of 20 s on-peak and 10 s off-peak, with a spot size of <1 µm and a beam current of 30 nA.

Initial recording measurements of the liquids were performed with identical counting times, a current of 10 nA and a spot size of 15 µm. Higher-precision measurements of MnO content were performed using higher currents and longer counting times. No difference in the accuracy or precision of MnO analyzes was found between the analyzes at 30 nA and 60 nA, and thus the data for MnO under both conditions were used, but only the data at lower currents were used for other oxides.

RESULTS

  • MnO partitioning in olivine
  • MnO partitioning in pyroxene
  • MnO partitioning in garnet
  • Bulk partitioning calculations
  • Other implications

In our experiments, MnO is significantly more compatible in olivine than in any experiment by Walter (1998) , but the measured partition coefficients lie in linear trends versus T , , or ( Figure 1 ). Our experiments show partition coefficients significantly below these values, close to the values ​​predicted from a linear fit of the data by Walter (1998). Melting of this source material with its high olivine content will produce a liquid with a lower FeO/MnO ratio than the source due to the high grade.

These numbers are consistent with our calculations of FeO/MnO ratios that would be produced by low-grade melting of a typical peridotite. As above, using the partition coefficients from Pertermann and Hirschmann (2003), even from their highest T measurement, only increases the FeO/MnO of the estimated pyroxenite melt and would thus require a reduction in the pyroxenite component of the source. Aqueous melting in the presence of garnet can produce. correlations between the FeO/MnO ratio and other indices indicating the presence of garnet in the melt source.

Measured values ​​of mineral/melt partition coefficients for clinopyroxene from this work (triangles), Walter (1998) (squares), and Pertermann and Hirschmann (2003) (blue diamonds). Garnet/melt partition coefficients fit a lattice-strain model of the form of Van Westrenen et al.

Table 1: Experimental data used in this study from samples where MnO contents were  measured using high-precision techniques
Table 1: Experimental data used in this study from samples where MnO contents were measured using high-precision techniques

Whole Rock Dy/Yb

ACTIVITY-COMPOSITION MODEL

The Au-Pd-Fe system shows negative deviations from the ideal Fe solution (i.e., the Fe activity is less than the Fe mole fraction) over the full composition range considered here; the deviation from ideality decreases with increasing Fe content. The deviation from ideality is smaller than that seen in the Pt-Fe system (Kessel et al. 2001). We note that the application of this solution model is only applicable to Fe-reactive Au75Pd25 alloys, but this is a common choice of capsule material and so this preliminary calibration should be useful in its own right.

XFe = 1 - XAuPd, (5) where γ is the activity coefficient for the component in solution, X is the measurement. We tried to fit our data to a regular symmetric solution, where WG2 = WG1, but the quality of the fit was poor compared to that in the asymmetric case including both parameters. These Margules parameters have lower absolute values ​​than those for the Pt-Fe system, again consistent with a less negative deviation from ideality and lower solubility of Fe in these AuPd alloys.

APPLICATION OF SOLUTION MODEL TO PREPARATION OF CAPSULES FOR FE-BEARING EXPERIMENTS

Under oxidizing conditions, a 1 log unit change in oxygen fugacity can correlate with a change in alloy composition by a factor of 2. While the buffering capacity of a capsule in any experiment depends on the ratio of capsule mass to sample mass, in all but the most oxidizing conditions or in samples with very low Fe content, a log unit change in fO2 should result in significant changes in the equilibrium alloy composition and probably also significant shifts in the Fe content of the sample. Further refinements and improvements to the MELTS algorithm will also improve the reliability of this calculation.

The pMELTS algorithm (Ghiorso et al., 2001) can be used for a more accurate calculation of the thermodynamic properties of liquids at pressures up to 3 GPa. Hirose (1994) Au-Pd sample containers for melting experiments on iron-water containing systems. 2001) Thermodynamic properties of the Pt-Fe system. Errors here are expected to be smaller than the symbol size (maximum 2σ values ​​~0.2 in ƒO2 and ~0.01 in Fe content).

Calculated a Fe

Mole Fraction Fe in AuPd sample

RTLn ɣ Fe(KJ/Mol)

Mol Fraction Fe in AuPd sample

RESULTS 1 Olivine regression analysis

  • Olivine abundance chronology
  • Historic flows
  • Olivine addition calculations

The differences in FeO* between volcanoes are small, and most of the volcanoes are statistically indistinguishable (Figure 3). All drill core data are included in Figure 2, but only for Mauna Kea do they constitute 50% or more of the available whole-rock analyses. The HSDP cores through Mauna Kea and Mauna Loa and the KSDP core through Ko'olau all produce trends that are indistinguishable within error from the trends seen in the full data sets from the same volcano, suggesting that. full datasets are representative of volcanoes' behavior over time.

First, the SOH-1 core through Kilauea has a lower olivine content than all other Hawaiian volcanoes sampled. However, the lowest part of the HSDP2 core again shows faster changes in olivine content. Analyzes of the available, well-dated historical flows for Mauna Loa and Kilauea are shown in Figure 7.

Gambar

Table 2: experimental results
Table 2: Full experimental results, concentrations given in weight percent. 2 samples do not have cpx analyses presented; the cpx  grains available were small and we were unable to obtain electron probe analyses that were not contaminated by the exterior q
Table 3: Our given liquid composition estimated to be an average hydrous liquid that could be produced by melting KLB-1 under the  pressure and temperature conditions used here
Table 1: Experimental data used in this study from samples where MnO contents were  measured using high-precision techniques

Referensi

Dokumen terkait

Characteristics of East Nusa Tenggara Station TVRI Employees Based on Staffing Status No Staffing Status Amount Percentage 1 Civil Servants 65 71% 2 Non-Civil Servants 27 29% 3