Supporting Information (SI) for
Volcanic history of the Imbrium basin: A close-up view from the lunar
rover Yutu
Jinhai Zhang, Wei Yang, Sen Hu, Yangting Lin, Guangyou Fang, Chunlai Li, Wenxi
Peng,Sanyuan Zhu, Zhiping He, Bin Zhou, Hongyu Lin, Jianfeng Yang, Enhai Liu, Yuchen Xu, Jianyu Wang, Zhenxing Yao, Yongliao Zou, Jun Yan, Ziyuan Ouyang
S1. Topographical features of the Chang’e-3 landing site ...... 2 S2. APXS experimental method ...... 3 S3. Geochemical features of Chang’e-3 landing site...... 8 S4. VNIS spectra decoding method...... 9 S5. Lunar Penetrating Radar data processing...... 15
S6. SI References...... 29
● Supplementary Figures S1 to S21
● Supplementary Tables S1 to S3
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S1. Topographical Features of the Chang’e-3 Landing Site Figure S1 shows the landing site of Chang’e-3 in the northeastern Imbrium basin. It locates on the young and high-Fe, high-Ti lava flow that overlying on the old and low-Ti basalt unit emerging about 10 km north. The young lava was dateed 2.0-2.3 Ga (1), and the old unit was dated 3.5 Ga (2). Another basalt unit, with intermediate FeO and
TiO2 contents (3) or referred to as higgh-Al (4), can be recognized (Fig. S1c). However, age of this intermediate basalt unit is indistinguishable from the old low-Ti basalt. From Apollo orbital photography, Schaber (5) outlined three main lava flows extended about 1200 km, 600 km, 400 km from the venting region near the Euleer crater 700 km southwest to the landing site, and they overlie on the old low-Ti basalt unit (Fig. S1b). Chang’e-3 landed on the youngest lava flow that extended 1200 km. The landing site has abundant rocky ejecta (Fig. S2), which cover about 5.7% of the surface.
Fig. S1. The geological map of Mare Imbrium, showing Chang’e-3 landed on the young high-Ti basalt unit that probably overlies on other two units. (a) The image of Mare Imbrium, taken by Chang’e-1; (b) Disstribution of three main lava flows originated from a venting area near the crater Euler, modified from (5); (c) Compositional map of basalt units, after (3); (d) Modal age map after (1), except for 3.5 Ga from (2).
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Fig. S2. Typical landscape at the Chang’e-3 landing site, showing abundant rocky ejecta.
S2. APXS Experimental Method The Active Particle-induced X-ray Spectrometer (APXS) was equipped on the robotic arm of Yutu, and it consists of a dual radioactive source of 55Fe (half-life of 2.73 year, 470 mCi) and 109Cd (half-life of 1.27 years, 45 mCi) and a Si-drift detector with an energy resolution of 135 [email protected] keV (6). The surfaces of targets were irradiated by the X-ray from decay of both 55Fe and 109Cd, and the fluorescent X-ray spectrum was counted by the Si-drift detector. The data used in this study are 2B level, which have been corrected for energy calibration, working distance, effect of temperature and dead time (6). Twelve elements, including Mg, Al, Si, Ca, Ti, K, Cr, Fe, Sr, Y, Zr and Nb, have been detected in the lunar soil at the landing site (Fig. S3). The K and K lines of Cu were from the device material, and K lines of Mn and Fe overlapped by Compton scattering peaks of the 55Fe source. Two APXS analyses of the lunar soil have been carried out, together with the measurements of the onboard basaltic working reference. All analyses have been corrected for background and peak overlapping. The compositions of the lunar soil were calculated from the net counts, calibrated with the onboard basalt reference and a set of standards that were measured in laboratory. S2.1 Measurements of the standards and working references in laboratory In order to calibrate the in-situ analyses of the lunar soil at the landing site, a total of 10 standard materials and working references have been measured in laboratory within a period from April 24, 2013 to July 2, 2014. These analyses were carried out in three
3 analysis sessions, using the onboard APXS or its duplicate (Table S1). The standards used in this study include one China National Standards basalt (GBW07105, also labeled as GSR-3 (7)), 2 Lunar Soil Simullants (CLRS-1, CLRS-2), 2 rock chips of lunar meteorites (NWA 2995, NWA 4734) and 5 terrestrial basalts (DC13-16R, NAO rock, DC13-08, 03JG-2, HBJ4-3). These standards and working references cover the compositional ranges of the lunar soil. The powder sample surfaces (60 mm in diameter) were strickled flat, and the measurements were carried out in a vacuum chamber. The working distance is about 10 mm. Each sample was counted for 30 minutes.
Fig. S3. The X-ray spectra of the lunar soil and the onboard basaltic reference analyzed by APXS on the rover Yutu. Ka and Kb lines of Cu are from the device itself, and Ka lines of Mn and Fe overlapped by Compton scattering peaks of the 55Fe source.
S2.2 Data processing Background of the X-ray spectra: The APXS data were processed using PyMca software (8). The continuum background was fitted using a linear function. For the dual radioactive sourrce, it is difficult to evaluate the spectral background theoretically, which is mainly contributed from elastic and inelastic peaks of the Fe and Cd sources, Compton scattering in the targets and the detector, and fluorescence of the major elements of the targeets. In order to find the smooth and best fitting background, sseveral empirical functions including none background, constant background, linear function, linear polynomial function and exponential polynomial function were applied, and the results are compared in Fig. S4. The major elements, including Al, Si, K, Ca, Ti and Cr, show nearly the same results for the different modes of background; whereas, Mg shows differences between the connstant or none background and the other background functions.
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In order to assess the fitting of background, we plotted the net peak areas of the elements versus the recommended concentrations of the standards and working references. It is found that the data can be best fitted by the linear model of background (Fig. S5).
Table S1. The information of the standards and working references. Chemical Analysis Sample Name Rock Type Form Composition session GBW07105 Basalt Powder (1) (a)(c) NAO powder Basalt Powder (2) (a) NAO rock Basalt Rock Chip (2) (a) NWA2995 Lunar Breccia Rock Chip (3) (b) NWA4734 Lunar Basalt Rock Chip (3) (b) DC13-16R Basalt Rock Chip (4) (b) DC13-16P Basalt Powder (4) (c) DC13-08 Basalt Powder (4) (c) 03JG-3 Basalt Powder (5) (c) HBJ4-3 Basalt Powder (5) (c) CLRS-1 Lunar Soil Simulant Powder (6) (c) CLRS-2 Lunar Soil Simulant Powder (7) (c) The experiments were carried out in 3 analysis sessions in ground laboratory: (a) April 24, 2013, with the onboard APXS; (b) December 20, 2013, with the duplicated APXS, and (c) July 2, 2014, with the duplicated APXS. (1) GBW07105 is a basalt of China National Standards; (2) NAO powder and NAO rock are the same basalt in different form, which was collected from Hannuoba, northeastern China, by National Astronomical Observatory (Report for CE-3 APXS scientific verification experiments, File Number: CE3-GRAS-CSSY-004-F2); (3) NWA2995 is a lunar feldspathic breccia, and NWA4734 is a lunar basalt (9); (4) DC13-08 and DC13-16 are low-Ti and high-Ti Emeishan flood basalts, respectively, collected from Dongchuan, southwestern China. DC13-16P and DC13-16R are powder and rock chip of DC13-16, respectively; (5) 03JG-3 and HBJ4-3 are Cenozoic basalts from western Liaoning, northeastern China (10); (6) CRLS-1 is China low-Ti Lunar Soil Simulant standard (Report for low-Ti basaltic lunar soil simulant standard CLRS-1); (7) CRLS-2 is the China high-Ti Lunar Soil Simulant standard (Report for high-Ti basaltic lunar soil simulant standard CLRS-2).
Peak overlapping correction: After background removal, the peak area fitting was performed within the range of channel 50 and channel 1300 (corresponding to energy from 0.70 keV to 16.80 keV) with Pseudo-Viogt functions. The peak area of each element was determined from the deconvolved peak. The uncertainties of the peak areas were estimated < 1-3% for Si, K, Ca, Ti and Fe, <6% for Al, <15% for Mg, < 10% for Sr, Zr and Cr, < 30-50% for Nb and Y. Calibration of decay of the radioactive sources: Since 109Cd source (half-life of 1.27 years) decays quickly than 55Fe source (half-life of 2.73 year), the relative peak counting rates of Fe, Sr, Y, Zr and Nb to those of other elements (the X-ray energy lower 5 than K line of Fe) vary with time. Therefore, the peak area of each element was calibrated to the same intensity of the radioactive source on April 24, 2013, assuming that the low energy X-ray lines of Mg, Al, Si, K, Caa, Ti and Cr were excited only by 55Fe source. Calibration by the standards and working references: After calibration of decay of the radioactive source, the net peak areas of the elements were normalized to the internal reference element, i.e., Mg, Al, K, Ca, Ti, Fe and Cr normalized to Si, whereas Sr, Zr, Y and Nb normalized to Fe. Figure S5 plots the abundance ratios versus the peak area ratios of these elements of the standards and working references. All of the elements show linear correlations, with the regression lines through the origin of coordinates. The two in-situ analyses of the lunar soil at the landing site were plotted in Fig. S5. It is noticed that both analyses are nearly identical to each other, indicative of homogeneity of the lunar soil. Only Y/Fe peak area ratios of both analyses show a significant difference. This is likely due to heterogeneity of phosphates (Y- and REE-bearing phases) in the lunar soil, instead of the analytical uncertainty. Using the calibration lines in Fig. S5, the in-situ analyses of the lunar soil at the landing site can be converted to the elemental abundance ratios. The composition of the lunar soil was then calculated by normalizing the analysis total to 100 wt%, and the results are listed in Table 1.
Fig. S4. Net peak areas of the elements, using different spectral background functions. The sample is the lunar soil LS2.
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Fig. S5. Calibration lines of the standards and working references. The peak area fitting was performed with Pseudo-Viogt functions, after linear function background removal. The vertical lines are the measured peak area ratios of the lunar soils.
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Fig. S6. FeO vs. Al2O3 plot of the lunar soil at Chang’e-3 landing site, in comparison with: (a) the Apollo lunar soil samples (11), and (b) lunar meteorites (9).
Fig. S7. Histogram of the TiO2 contents of the rims and proximal ejecta of small craters (0.4–4 km). The smaller craters (0.4–1 km) display a peak at ~5 wt% TiO2, and with a nearly flat tail at the lower side. The low TiO2 peak is attributed to the underlying low-Ti basalt excavated by the larger craters. The TiO2 content of the lunar soil at the landing site is indicated by arrow. The TiO2 data of the ejecta of small craters are from (4).
S3. Geochemical Features of Chang’e-3 Landing Site
The lunar soil at Chang’e-3 landing site contains higher FeO and lower Al2O3 than those of Apollo mare soils, plotting within the range of mare basalts (Fig. S6). This result suggests that the lunar soil at Chang’e-3 landing site contains little feldspathic ejecta, which could represent the beneath lava flow. The FeO and TiO2 contents of the lunar soil fill the gap between the high-Ti and low-Ti basaltts (Fig. 3b) (12). The trace incompatible lithophile Y and Zr deviate from Apollo basalts, but can be explained by assimilation of the KREEP component (Fig. 3a) (4).
The TiO2 contents of the rims and proximal ejecta of small craters (0.4–4 km) on the young lava flow have been determined with compositional remote sensing data from
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Lunar Prospector Gamma Ray Spectrometer and Clementine (4). The TiO2 content distribution patterns are related with the sizes of the craters (Fig. S7). The smallest craters
(0.4–1 km) show a high-TiO2 peak at about 5 wt% with a flat and low-TiO2 tail. This distribution pattern can be decoded into a high-TiO2 peak and another low-TiO2 peak. The high-TiO2 peak is similar to the in-situ analysis by Yutu and to the whole surface TiO2 distribution (13), suggesting that the smaller craters have not penetrated the most upper high-TiO2 basalt unit. In other words, the thickness of the high-TiO2 basalt unit should be significantly larger than 120 m, the depth of a crater with a diameter of 0.4 km.
The low-TiO2 peak indicates that the other craters have excavated the beneath low-Ti basalt unit. This is confirmed by the low-TiO2 content distribution of the large craters (1– 4 km), which penetrated even deeper and excavated the underlying low-TiO2 basalt unit emerging about 10 km north from the Chang’e-3 landing site (Fig. S1c). The depth of 270 m was calculated for a crater with a diameter of 1 km using the lunar crater mode (http://www.lpi.usra.edu/lunar/tools/lunarcratercalc/), which can be referred to as the maximum depth of the high-TiO2 basalt unit.
S4. VNIS Spectra Decoding Method The mineral modal composition of the lunar soil can be decoded using the modified Gaussian Model (MGM) method from the four VNIS spectra, and the results are summarized in Table S2. The average lunar soil contains 16.4 vol% plagioclase and 17.9 vol% pyroxenes. A modal abundance of 6.3-8.8 vol% ilmenite can be estimated from the
TiO2 content measured with APXS, assuming most TiO2 in ilmenite. This modal composition is consistent with that of the average Apollo mare soils. The FeO contents of the lunar soil was determined from the correlation between FeO contents and Fe values of the Apollo soils, where Fe= -arctan((R945/R750-1.22)/(R750-0.04)) (14, 15), ranging from 18.7 wt% to 19.5 wt% with an average of 18.9 wt%. The decoded FeO content of the lunar soil is consistent with the APXS results within the analytical uncertainties. The
TiO2 contents of the lunar soil can also be determined from the spectra, based on the correlation between the TiO2 contents and the Ti values, where Ti = arctan ((R415/R750-0.42)/(R750-0.00)) (14, 15). The TiO2 contents vary from 5.3 wt% to 9.0 wt%, with an average of 6.6 wt%. The TiO2 contents are higher than the APXS analyses, which might be due to the rough surface of the landing site, which leads to part of the analysis areas darker due to shadow (Fig. S8).
S4.1 Correction of the VIS/NIR and SWIR spectra The onboard VNIS was installed at the front of the rover Yutu, and it consists of a VIS/NIR imaging spectrometer (450–945 nm) and a shortwave IR (SWIR) spectrometer (900–2395 nm) (16). The VIS/NIR data were recorded as images of 256×256 pixels, with a spatial resolution of ~0.6 mm. The SWIR data were integrated from a round area with a radius of 54 pixels, whose center corresponds to the pixel (128, 96) of the VIS/NIR
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image. Four analyses have been carried out, and the analysis positions are labeled in Fig. 2. Each of the VIS/NIR image was integrated for 40 min (except for CD006: 18 min, and CD007: 31 min) and each of the SWIR spectrum was integrated for 32 min (except for CD006: 8 min), respectively. The spectrum resolution is 2–7 nm for VIS/NIR and 3–12 nm for SWIR spectrometer. The data have been corrected for dark current, the effect of temperature, radiometric and geometric calibrations, and released as 2B level (17). The 2B level VIS/NIR data were sequentially reduced to repair bad lines (pixel gray-scale slope threshold method) and bad points (discretely bright pixels), to make flat field corrections (global histogram equalization) (18), and then the data were converted to reflectance. The SWIR radiance was directly converted to reflectance. Both VIS/NIR and SWIR reflectances have been calibrated for incident angles of light and solar irradiances (19). The corrected VIS/NIR images are shown in Fig. S8. As VIS/NIR and SWIR spectra were separately measured with different spectrometers, there was discontinuity between them (900–945 nm). An offset was applied to the SWIR spectrum, which shifted the spectrum continuously to the VIS/NIR spectrum. The offset value was determined by minimizing the standard deviation (equation 1) between the overlapping wavelengths.
Table S2. The decoded results from the VNIS spectra of the lunar soils. * Distance R Ti TiO2 Fe FeO OMAT Plagioclase Pyroxene 450 415 750 950 (m) (nm) (nm) (nm) (nm) (wt %) (wt %) (vol %) (vol %) CD005 19.79 0.043 0.039 0.070 0.0611 1.175 5.8 1.487 18.8 0.312 15.0 20.6 CD006 32.06 0.033 0.030 0.057 0.0594 1.154 5.3 1.482 18.7 0.157 16.6 20.3 CD007 38.72 0.027 0.025 0.047 0.0489 1.195 6.4 1.534 19.5 0.158 17.5 17.8 CD008 40.89 0.032 0.029 0.051 0.0559 1.274 9.0 1.489 18.8 0.098 16.3 13.0 Avg. 6.6 18.9 0.181 16.4 17.9 *Distance from the lander; OMAT: optical maturity parameter.
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Fig. S8. Micrographs of the lunar soil at the Chang’e-3 landing site, showing a rough surface with shadow areas. The width of the field is ~150 mm.
945 2 error R offset R / N 1 (1) VIS/NIR SWIR 900 Where error is the standard deviation between the overlapping wavelengths of VIS/NIR and SWIR spectra, N is the band number of the overlap (N=10), is the wavelength in nm with 5 nm interval, RVIS/NIR() is the reflectivity of VIS/NIR at , and RSWIR() is the reflectivity of SWIR at . The best offsets of CD005–008 are -0.00459, 0.00987, 0.0094 and -0.00655, respectively.
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Fig. S9. The calibration curves for TiO2 and FeO contents, derived from the spectra of Apollo soils measured in laboratory (20, 21).
S4.2 TiO2 and FeO contents achieveed from the VNIS spectra The TiO2 content of the lunar soil correlates with the reflectance ratio between bands at
415 and 750 nm, R415/R750, via Ti parameter, Ti (Fig. S9a). The parameter Ti is defined by Ti=arctan[(R415/R750-y0Ti)/(R750-x0Ti)] after Lucey et al. (15), and the R415 was 2 determined from R450 by R415=0.95R450-0.0013 (R =0.99) derived from the spectra of Apollo lunar soils (20), where y0Ti=0.40 and x0Ti=0.0 were optimized to maximize the correlation coefficient between TiO2 contents and Ti of Apollo soils with grain size < 45µm (20, 21). The TiO2 contents of the lunar soil were 5.3–9.0 wt% with an average of 5.44 6.6 wt%, calculated using the best fit curve of TiO2 (wt%)=2.416Ti (Fig. S9a). The calculated TiO2 contents are somewhat higher than the APXS analyses, likely due to shadow effects of the rough surface of the landing site (Fig. S8). Similarly, tthe FeO contents of the lunar soils can be determined from the best fit curve of FeO (wt%)=16.103Fe-5.18 (Fig. S9b), where Fe is defined by Fe=-arctan[(R950/R750-y0Fe)/(R750-x0Fe)] after Lucey et al. (15), and y0Fe=1.23 and x0Fe=0.04 were optimized to maximize the correlation coefficient between the FeO contents and Fe of Apollo lunar soils with grain size < 45µm (20, 21). The R950 value is nearly identical to R945, based on the spectra of Apollo lunar soils (20). The FeO contents of the lunar soil are 18.7–19.5 wt% with an average of 18.9 wt%. These calculated FeO contents are consistent with the APXS measurements within the analytical uncertainties.
S4.3 Major constituent mineral abundance deconvolution The mineral compositions of the lunar soils were deeconvolved from the VNIS spectra using the Modified Gaussian Model (MGM) (22). The possible constituents of the lunar mare soils include impact-induced agglutinate glasses, high-Ca and low-Ca pyroxenes and plagioclase, with minor ilmenite, olivine and volcanic glass (21). Both
12 agglutinate glass and ilmenite have no absorption around 1 m and 2 m bands, and olivine is a minor phase in the lunar mare basalts (<5 vol%) (21). These constituents were not considered in the MGM fitting calculation. In this work, four of the absorption peaks of pyroxenes (orthopyroxene and clinopyroxene)), the absorption peak of plagioclase at 1.25 m and one more peak below 0.5 m were used as the starting parameters for MGM fitting. Figure S10 shows the results of the deconvolution, with all four spectra well fitted.
Fig. S10. MGM deconvolution of the lunar soil spectra at the landing site.
In order to determine the mineral contents of the lunar soils, we processed the spectra of the Apollo soils reported by (20) with the known mineral compositions (21), using the same MGM. Figure S12 plots the deconvolved absorption band strength of pyroxene and plagioclase versus their abundances, respectively. The calibrated spectra are similar to the laboratory measurements of Apollo mare soil samples, showwing absorption at 1 µm and 2 µm responding to the presence of pyroxene and plagioclase (Fig. S11). Based on the correlations of the Apollo soils (Fig. S12), the mineral compositions of the lunar soil at the Chang’e-3 landing site were determined with 17.9 vol% pyroxene (13.0–20.6 vol%) and 16.4 vol% plagioclase (15.0–17.5 vol%) (Table S2).
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Fig. S11. Reflectance specttra of the lunar soil meaasured in situ by the rover Yutu.
Fig. S12. Plot of mineral abundances of the Apollo soils versus its natural log band strengths deconvolved from the spectra using MGM method. (a) pyroxene as suum of orthopyroxene and clinopyroxene at 1 m; (b) plagioclase at 1.2 m. The Apollo data from (20, 21).
S4.4 The maturity of the lunar soil The optical maturity (OMAT) of the lunar soil was calculated from the equation of