Decoupled isotopic record of ridge and subduction zone processes in oceanic basalts by independent component analysis
Abstract
[1] Isotopic variability in oceanic basalts indicates possible interactions among multiple mantle components or geochemical end-members. Beyond the standard principal component analysis, which has been used so far to identify mantle components, the relatively new independent component analysis is well suited for extracting independent features in multivariate compositional space. Radiogenic isotopic compositions of oceanic basalts from the Atlantic and South Indian oceans, including both mid-ocean ridge basalts (MORB) and ocean island basalts (OIB), show that two independent compositional vectors (referred to as independent components or ICs) account for most of the observed variations with three isotopic ratios of Pb (856 MORB and 781 OIB) or five isotopic ratios of Pb, Sr, and Nd (672 MORB and 597 OIB). In both cases, the first IC distinguishes OIB from MORB, while another maps the geographical distribution of a mantle component and in particular the DUPAL anomaly. This property shows that the two ICs indeed distinguish independent information and reflect two distinctive geodynamic processes, a feature which is not present in the conventional analysis of mantle isotopic variability. The first IC that distinguishes OIB from MORB is similar to the isotopic trend reproduced in the MORB-recycling model of Christensen and Hofmann (1994). The second IC that discriminates geographical distribution is characterized by simultaneous enrichment/depletion of Pb, Rb, and Nd relative to U-Th, Sr, and Sm, respectively, which can be explained by elemental fractionation associated with aqueous fluid-mineral reactions. These geochemical characteristics, together with the fact that most of the observed multidimensional isotopic space is spanned by the joint distribution of the two ICs, indicate independent but overlapping differentiation processes which mostly take place within the depleted mantle domain. They are likely to reflect ridge versus subduction zone processes, or melting versus interaction with aqueous fluid. We use the regional distribution of the second, “enriched” IC to redefine the DUPAL anomalous mantle and show that in addition to its Southern Ocean type locality, it also distributes itself broadly in the Northern Hemisphere.
1. Introduction
[2] One of the well-accepted concepts of mantle isotope geochemistry is that the isotope compositions of radiogenic elements (e.g., Sr, Nd and Pb) in terrestrial basalts can be broken down into individual mantle components. These components are inherited from geochemical reservoirs with a distinctive history, such as ancient residues of melting at ridge crests or recycled oceanic crust, and with characteristic isotopic properties resulting from long-term isolation. The geochemical nature and spatial distribution of these components are thought to provide key information on differentiation and convection of the Earth's mantle. For this reason, extensive efforts have been made to identify the geochemical mantle components present in mid-ocean ridge basalts (MORB) and ocean island basalts (OIB) [e.g., White, 1985; Zindler and Hart, 1986; Hofmann, 1997].
[3] Principal component analysis (PCA) has been regarded as the most efficient way to identify these mantle components [e.g., Zindler et al., 1982; Allègre et al., 1987; Blichert-Toft et al., 2005]. Principal components are those linear combinations of observables with the largest possible variance. As will be shown later, however, the core assumption of PCA, which holds that the data constitute a single multivariate Gaussian population, is clearly invalidated for the isotope compositions of oceanic basalts. In this case, the principal components (PCs) do not form a true base, i.e., a set of independent vectors describing uniquely the isotopic variability. A promising tool for the analysis of geochemical mantle components is independent component analysis (ICA), which has been established in Information Science over the past ∼15 years (e.g., see the textbooks by Hyvärinen et al. [2001] and Amari [2002]). As with PCA, the core assumption is that the data can be accounted for by a linear combination of mutually independent components, but without the condition that the population is unique with a multivariate Gaussian distribution. ICA deconvolves a data set into independent components (ICs) by finding the directions that maximize the non-Gaussianity through criteria such as a higher-order cumulant or negentropy (see below) of the projected data distribution [Hyvärinen et al., 2001]. A caveat is that the term “component” as used for both PCA and ICA refers to a vector or a direction, which unfortunately conflicts with the well-entrenched denomination of geochemical mantle components. In order to avoid such confusion, we hereafter use “component” for describing the statistical distribution in both PCA and ICA and “end-member” for the geochemical mantle components with specific compositions, such as Depleted MORB Mantle (DMM).
[4] The relevance of statistical distributions, typically normal versus lognormal, underlying elemental and isotopic data on oceanic basalts has been discussed by different authors under different perspectives. Allègre and Lewin [1995] investigated different geochemical properties in basalts and concluded that the underlying distributions could be normal, lognormal, fractal or multifractal. Meibom and Anderson [2004] conjured up the central limit theorem to argue that the complexity and multiplicity of melting and mixing events in the mantle lead to near-Gaussian histograms. Rudge et al. [2005] argued that isotopic ratios are not normally distributed and analytically elaborated statistical distributions from melting-recycling models. They derived expressions for the higher central moment and particularly the skewness of the distributions of isotopic ratios, which provides a background theory for non-Gaussian histograms. These authors only considered models with linearized radioactive decay, a constraint later released by Rudge [2006]. By examining databases, Albarède [2005] used statistical tests (notably quantile-quantile plots and comparison between corresponding means and modes) to show that normal distributions do not do justice to actual histograms of isotopic ratios in MORB. We will see in particular that the non-Gaussianity of isotope distributions appears nowhere more clearly than in two-dimensional diagrams of Pb-isotopic ratios in oceanic basalts.
[5] In this study, we examined the compositional space of a maximum of six isotopic ratios (204Pb/206Pb, 207Pb/206Pb, 208Pb/206Pb, 87Sr/86Sr, 143Nd/144Nd, 177Hf/176Hf) with an algorithm known as FastICA [Hyvärinen, 1999] for oceanic basalts from the Atlantic and South Indian oceans. The data set includes both MORB from the literature [Agranier et al., 2005; Meyzen et al., 2005, 2007, and references therein] (most of which can be found in the PetDB database http://www.petdb.org) and OIB from GEOROC database (http://georoc.mpch-mainz.gwdg.de/georoc/). On the basis of the geochemical characteristics of the two ICs in the five-dimensional space of Pb-Sr-Nd isotopic ratios, the origin of isotopic heterogeneity and the differentiation processes of the mantle are discussed. The detected ICs naturally leads to redefinition of the DUPAL anomaly, showing that the enriched signature distributes broadly into the Northern Hemisphere.
2. Principles of Independent Component Analysis





[7] First, the observed multivariate variables and data (e.g., x1 and x2 in Figure 1b), which are assumed to be linear mixtures of unknown independent variables, are centered and scaled by the standard deviations along the PCs. This procedure is called “whitening” [e.g., see Hyvärinen et al., 2001, chapter 6], and transforms the variables and the data in Figure 1b to those in Figure 1a where the transformed variables x1′ and x2′ and the two PCs lie along the diagonal axes. In this whitened space of Figure 1a, any orthogonal pair of two variables, including x1′ and x2′, are uncorrelated but not necessarily independent. ICA searches for the independent pair from these orthogonal pairs by maximizing non-Gaussianity instead of maximizing variance as for PCA. Figure 1c shows the marginal probability density corresponding to the joint distribution shown in Figure 1a: ps1 (s1) (probability density projected on s1, red line) and px1′ (x1′) (that projected on x1′, green line) are plotted, together with a Gaussian distribution (black line) plotted for reference. It shows that ps1(s1) deviates significantly from the Gaussian distribution (large non-Gaussianity), whereas px1′ (x1′) deviates to a lesser extent (smaller non-Gaussianity). In the whitened space, the independent components have the maximum non-Gaussianity of all the possible sets of uncorrelated components. This is because, according to the central limit theorem, random mixing of non-Gaussian variables approaches Gaussian more than the original variables. Therefore, a linear combination of s1 and s2 (i.e., Σiaisi, where ai are the mixing coefficients), such as x1′ or x2′ in Figure 1a, are closer to Gaussian than si.
[8] In turn, a linear combination of the observed mixture variables (e.g., Σibixi′, where bi are the mixing coefficients) will be maximally non-Gaussian if it equals to one of the independent components [Hyvärinen et al., 2001, chapter 8]. In the example of Figure 1a, x1′ and x2′ are rotated around the center to find the ICs (i.e., s1 and s2) that give maximum non-Gaussianity. Then the ICs can be linearly backtracked to the original space (e.g., s1′ and s2′ in Figure 1b). The two ICs are therefore nonorthogonal in the original space (Figure 1b), which contrasts with the orthogonal relationship between PCs. Independent components may be orthogonal, but on the condition that the variables are uncorrelated Gaussian variables. In such a case, however, non-Gaussianity is zero for all the components and ICA cannot extract a unique set of ICs. Nonorthogonal ICs in the original space and oblique PCs with respect to ICs therefore reflect the non-Gaussian character of the observed data. We will show the data distribution and the extracted ICs in both original and whitened spaces in the following analyses of the oceanic basalts.
[9] Whitening removes correlation from the original data set and also determines the proportion of the total variance that the components account for. As is commonly assumed in both PCA and ICA, components which account for a small proportion of the variance are judged to be unimportant signals. In this study we follow this conventional procedure to determine the number of ICs, although ICA can potentially extract ICs as many as the number of the observed variables based on non-Gaussianity criteria.




3. Independent Components of Isotopic Compositions of Oceanic Basalts
[11] In total, 1637 data sets are available with the three Pb isotopic ratios (856 MORB and 781 OIB), while 1269 data sets are available with the five ratios of Pb, Sr and Nd (672 MORB and 597 OIB), and 461 data sets exist for all six ratios (393 MORB and 68 OIB) (Figure 2). First, we examine the three Pb-isotopic ratios, for which mixing of different mantle geochemical end-members forms a truly linear trend suitable for ICA, as a large number of high-quality data recently have become available. Because counting statistics and thermal noise affect small signals much more so than strong signals, couples of isotopic ratios with a minor or otherwise noisy isotope as the denominator, such as 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb, are strongly correlated. Albarède et al. [2004] calculated the correlation coefficient between 206Pb/204Pb and 207Pb/204Pb introduced by Poisson counting statistics on 204Pb variables and found it equal to 0.96. Such a correlation of purely analytical origin interferes with geochemical correlations, e.g., because of the mixing of mantle geochemical end-members. The effect of analytical error correlations is particularly critical because the range of 207Pb/204Pb variations cannot be neglected with respect to analytical errors. In contrast, the correlation coefficient between 204Pb/206Pb and 207Pb/206Pb due to counting statistics is only 0.16, which makes the correlation between counting uncertainties essentially negligible with respect to those of more geochemical significance. The normalization to 206Pb is routinely used for early Solar System chronology and the parameters of the 207Pb/206Pb versus 204Pb/206Pb isochron are easily derived from those of the more conventional 207Pb/204Pb versus 206Pb/204Pb isochron [Tera and Wasserburg, 1972] (see Appendix A). For these reasons, we use 206Pb as the denominator for the Pb isotopic ratios, although the detected ICs are almost identical in both 206Pb- and 204Pb-normalized spaces (Appendix A and Figure A1).

[12] The principal components are determined for reference (Figure 3). The first component, PC1 (97.3% of the population variance), corresponds to the longest axis of the overall data distribution as it is defined to give the maximum variance of the projected data. However, the second component, PC2 (2.7% of the population variance), is not useful in describing the data, either individually or in groups. These features are similar to those determined for North Atlantic MORB [Blichert-Toft et al., 2005]. Two independent components (ICs), i.e., independent compositional base vectors to represent the observed compositional space, also cover 99.9% of the population variance, but are clearly oblique with respect to the PCs (Figure 3a).

[13] This feature is similar to Figure 1b in the simple example for homogeneous joint distribution. Although the overall elongation of data distribution in the original space obscures the relationship between the PCs and ICs, the obliquity is obvious in the whitened space (Figure 3b), where the data points and vectors are broken down into the two ICs. The obliquity between PCs and ICs always occurs when the data constitute a multivariate non-Gaussian population. Figure 3b is similar to Figure 1a (homogeneous joint distribution of the two independent components in the whitened space) in terms of the overall data distribution and the two PCs close to the diagonal axes, indicating that the observed isotopic data is clearly non-Gaussian.
[14] In Figure 3b, most OIB lie in the field of positive IC1 values, except for Iceland, which is situated on a spreading ridge, whereas most MORB have negative IC1, except for the plume-influenced ridge basalts [e.g., Schilling, 1973; White et al., 1976; Hanan et al., 1986]. In contrast, IC2 discriminates the geographical distribution: most of the basalts from northern and central latitudes have negative IC2 values, while basalts from the South Atlantic and Indian Ocean mostly plot in the field of positive IC2 values. Such a clear separation indicates that, contrary to the PCs, the two ICs may be independent and reflect the effect of two separate geodynamic processes to span most of the observed compositional space. On the other hand, although a linear trend nearly parallel to IC2 through EM-I (enriched mantle 1 [Zindler and Hart, 1986]), FOZO (focal zone [Hart et al., 1992]) or C (common component [Hanan and Graham, 1996]), and HIMU (high-U/Pb mantle [Zindler and Hart, 1986]) roughly limits the data distribution on the positive-IC1 margin, some data lie outside the polyhedron defined by connecting the conventional mantle geochemical end-members, especially for negative IC1 values. This indicates that mixing of the end-members cannot fully explain the observed compositional space. An alternative interpretation of Figure 3b will be proposed later.
[15] As a next step, the five-dimensional isotopic space with Pb, Sr and Nd was explored using ICA, and again two dominant components were identified, which together account for 97.7% of the population variance. An additional 1.9% of the total variance is covered by inclusion of the third component. It is not clear whether such a small share actually indicates the presence of an additional geochemical component or reflects the nonlinear character of mass balance relationships in 5 dimensions including Sr and Nd. The inclusion of three components creates metastable solutions that locally maximize non-Gaussianity, indicating that the major robust features are adequately represented by the two ICs shown in Figure 4.

[16] This result, i.e., the presence of only two major components covering more than 90% of the population variance, has already been shown by PCA for oceanic basalts [Zindler et al., 1982; Allègre et al., 1987; Hart et al., 1992], although the ICs are different from the PCs (Figure 4e). The two ICs in the space with five isotopic ratios are essentially the same as in Figure 3: IC1 separates OIB from MORB, and IC2 discriminates geographical distribution in both the OIB and MORB fields. We checked that essentially the same result is obtained for the subspace with only the three variables 204Pb/206Pb, 87Sr/86Sr and 143Nd/144Nd and with the four variables of the three Pb plus Nd isotopic ratios, which shows the robustness of the two ICs.
[17] The conventional mantle geochemical end-members do not span the entire space of observed compositions (Figure 4e). In addition, in the original space (e.g., Figures 4a–4d), some of the conventional end-members significantly deviate from the two-dimensional plane spanned by the two ICs. Note that, in Figures 3–5, the labels “IC1” and “IC2” are placed along the positive axes of ICs. EM-I and EM-II, which refer to those suggested by Zindler and Hart [1986] on the basis of extensive extrapolation of the data trends, plot in the field with positive IC1 and positive IC2, but do not plot in the same field in Figure 4d (and Figure 4b for EM-I). Assuming a 143Nd/144Nd for EM-I, its 87Sr/86Sr should be more radiogenic (by ∼0.002) if it is to be consistent with the actual data (Indian MORB or OIB) and the IC axes, i.e., to plot in the IC plane. Similarly, EM-II should correspond to lower 87Sr/86Sr values (by ∼0.002) so as to plot in the IC plane. In contrast, HIMU, FOZO/C and DMM plot consistently in all the diagrams: HIMU and FOZO/C plot in the field of positive IC1 and negative IC2, while DMM (D-DMM and A-DMM) falls along the IC1 axis. These end-members plot within the actual data or on a slight extension of the actual data trends and therefore plot in the two-dimensional IC plane, which accounts for 97.7% of the population variance. A slight deviation from the plane, however, distorts the data plot in the view nearly parallel to the IC plane: in Figure 4d, some of the Indian OIB (blue dots) plot slightly above the plane toward higher 87Sr/86Sr and 143Nd/144Nd values, which makes them appear closer to the IC2 axis.

[18] We also explored the six-dimensional space by adding Hf to the previous isotopic systems (Figure 5). Again two dominant components are identified, which together account for 95.2% of the population variance. However, in this case, the two calculated ICs are different from those of Figures 3 and 4, and are closer to the PCs (Figure 5g). The clear MORB-OIB separation and geographical discrimination are lost in the process. The geometries of data distribution and two ICs in the diagrams of Pb-Nd isotopic ratios (Figure 5c) and Pb-Hf isotopic ratios (Figure 5d) are similar, which is consistent with a high correlation between Nd- and Hf-isotopic ratios with almost identical slopes of the two ICs (Figure 5f). Also, most of the population variance (95.2%) is covered by the two components, which is similar to the result in the five-dimensional space with Pb-Sr-Nd isotopic ratios in Figure 4. A remarkable difference between Figures 4 and 5 lies with the number of data: because Hf isotope analysis has only recently become routine, the number of MORB data (393) far exceeds that of OIB data (68) (Figure 5), which contrast with the more balanced situation when Hf is omitted with 672 MORB and 597 OIB data (Figure 4). This imbalance significantly modifies the overall as well as internal structures of the data distribution, and results in the different ICs in Figure 5 relative to those in Figure 4. A larger number of data sets with the complete six isotopic ratios is nevertheless required to judge whether, as argued by Salters and Hart [1991] and Blichert-Toft et al. [2005], the Hf-isotopic ratio contains statistically unique information distinct from the information conveyed by the Pb-Sr-Nd systems.
4. Discussion
[19] Since ICA uses non-Gaussianity criteria throughout, a preliminary question is whether the data can safely be considered as nonnormal. In spite of convective stirring, the mantle is not homogeneous because new heterogeneities are continuously created by melting at ridges and subduction of the oceanic plates. As shown by Rudge et al. [2005], such a regime tends to a steady state, and the resultant distribution of geochemical variables are skewed and non-Gaussian.
4.1. Origin of Geochemical Independent Components
[20] The conventional view of mantle geochemical end-members is that their compositions are unique, although such compositions are only loosely constrained, namely by using either extreme data or an extension of observed trends where no actual datum exists. There is room, therefore, for shifting the composition of some mantle geochemical end-members to make them suitable as components of the ICs, as was discussed for EM-I and EM-II in the previous section. By contrast, the present study suggests that the literature mantle geochemical end-members may not necessarily represent unique compositions. The essential feature of Figure 3b and Figure 4e is that the variations along the two IC directions are created by two independent processes. When these two processes overlap, they will create the observed compositional variability. The ICA shown in Figures 3 and 4 suggest that the two components that have been identified are independent, which we take as an indication that they were created by distinct geodynamic processes. Since MORB and OIB roughly are symmetrically distributed around a depleted mantle composition in the IC space (although it is slightly more enriched compared to the average depleted MORB mantle (A-DMM) [Workman and Hart, 2005] as in Figure 4e), we argue that these processes occur as two differentiation processes mostly within the depleted mantle domain. The dual structure of the geochemical data demonstrated by ICA is robust and suggests that it reflects the two dominant geodynamic processes with distinct elemental fractionation processes in the Earth, the ridge and subduction zone processes. In addition, the overlap of two independent components reflects mutual processing: products from ridge activity are processed at subduction zones and ridges potentially remelt materials recycled through the subduction zones.
[21] Segregation and long isolation of MORB/eclogite from its harzburgitic residue and subsequent recycling can reproduce a broad trend in the Pb and Nd isotope space observed in oceanic basalts [Christensen and Hofmann, 1994], whose slope is similar to the IC1 direction. For example, in Figure 4c (204Pb/206Pb versus 143Nd/144Nd), the isotopic variation produced in the MORB-recycling model, which is slightly curved because of the faster rate of 238U decay relative to 147Sm [Christensen and Hofmann, 1994], is nearly parallel to IC1. The slopes of IC1 in Figures 4a–4d suggest that IC1 originates from elemental fractionation associated with simultaneous increases (or decreases) in U/Pb, Th/Pb, Rb/Sr and Nd/Sm, which is consistent with that associated with melting [e.g., Beattie, 1993; Green, 1994; Salters and Longhi, 1999]. Although the range and slope of the trend depend on several physical parameters such as density contrast between MORB/eclogite and peridotite, the MORB/eclogite-rich portion can form a source region of OIB, whereas the residual harzburgitic portion represents DMM [Christensen and Hofmann, 1994]. These features coincide with those of IC1, separating OIB from MORB.
[22] What IC2 reflects in contrast is likely to be subduction zone processes. In Figures 4b and 4c, the slope of IC2 has an opposite sign to that of IC1 and MORB-recycling trend that reflects elemental fractionation associated with melting, while both IC1 and IC2 exhibit the same sign in Figures 3a, 4a, and 4d. These features indicate that IC2 originates from elemental fractionation with simultaneous increases (or decreases) in Pb/U, Pb/Th, Rb/Sr and Nd/Sm. Such fractionation can occur associated with aqueous fluid-mineral reactions [Brenan et al., 1995; Keppler, 1996; Kogiso et al., 1997], and therefore suggests that aqueous fluid processes in subduction zones create the IC2 variation superimposed on the IC1 variability.
[23] Dehydration of the subducted oceanic crust concentrates more Pb, Rb and Nd in the aqueous fluid than U-Th, Sr and Sm, respectively, leading to a negative IC2 value of the dehydrated rocks, while hydration of the rocks can produce positive IC2. Clear differences between IC1 and IC2 also exist in relative magnitude of fractionation between the different parent/daughter pairs. Figures 3a, 4a, and 4d show that a differentiation process responsible for the IC2 variation fractionates U/Pb more than Th/Pb, and Rb/Sr more than Nd/Sm when compared to IC1. These differences can be explained by some of the experimental results on elemental partitioning among aqueous fluids, silicate melts and minerals [e.g., Beattie, 1993; Green, 1994; Brenan et al., 1995; Keppler, 1996; Kogiso et al., 1997; Salters and Longhi, 1999], although they are not readily inferred consistently from all the experimental data, since the partition coefficients significantly vary depending on a number of parameters, such as pressure, temperature, bulk composition, oxygen fugacity, alkali-chloride contents in fluids, mineralogy of the coexisting solid, and experimental configurations (e.g., static equilibrium or dehydration mobility experiments). However, considering the robust feature with simultaneous increases (or decreases) in Pb/U, Pb/Th, Rb/Sr and Nd/Sm, and that it must reflect a first-order differentiation process within the depleted mantle domain as dominant as ridge melting, we propose that IC2 is related to aqueous fluid processes in subduction zones as follows.
[24] During subduction of oceanic plates, altered MORB and oceanic mantle generate aqueous fluids and leave residues of dehydration. Fluids migrate upward and hydrate the overlying mantle wedge that may also contain recycled MORB and residual rocks circulated by corner flow, and cause flux melting and arc magmatism [Iwamori, 2007]. Hydration and dehydration at subduction zones of both the basaltic and refractory parts of the oceanic lithosphere and in the mantle wedge accounts for the overprinting of the IC1 geochemical variability by a distinct IC2 signature. The ubiquitous presence of this IC2 component in the source of both OIB and MORB (Figures 3b and 4e) simply reflects that most of the subducted oceanic lithosphere and the overlying mantle wedge go through the hydration-dehydration processes at subduction zones [Iwamori, 2007], in agreement with Li isotope evidence [Elliot et al., 2006].
[25] Melting in subduction zones also contributes to mantle differentiation, producing the continental crust and a residue [Tatsumi, 2000]. In terms of the nature of elemental differentiation, which reflects the effect of mineral/melt partitioning, the effect of melting in subduction zones may be similar to that at mid-ocean ridges. In fact, EM-II, which is analogous to continental crustal material recycled in the mantle [White and Duncan, 1996], has a positive IC1 and IC2 value (Figures 3b and 4e), reflecting both melting and aqueous fluid processes in subduction zones. Therefore, IC1 probably reflects melting processes, whereas IC2 reflects interaction of the mantle with aqueous fluid, regardless of the geodynamic sites where these processes take place. It is unclear at this stage how exactly the two elementary processes are separated in the IC space, partly because the aqueous fluid and melting processes are strongly coupled in subduction zones, as is suggested by numerical modeling of H2O transportation and melting in subduction zones [Iwamori, 1998], trace element modeling of aqueous fluid, peridotite and island arc basalts [Ayers, 1998], and (231Pa/235U)-(230Th/238U) variations of arc lavas [Thomas et al., 2002].
4.2. Geodynamic Implications
[26] The nature and possible origin of the ICs have several geodynamic implications. The existence of FOZO, or C, and the local trends toward it [Hart et al., 1992; Hanan and Graham, 1996] have been interpreted as representing mixing between the ambient mantle and a plume, or a diapir, rising from the core-mantle boundary [Hart et al., 1992] or the transition zone [Hanan and Graham, 1996]. In the IC space, FOZO, or C, is characterized by a positive IC1 and negative IC2 value (Figures 3b and 4e), corresponding to the melt component-rich (e.g., MORB/eclogite-rich) portion that has experienced dehydration in subduction zones, e.g., subducted oceanic crust. Because of its high density and viscosity, the subducted oceanic crust can be segregated from the subducted oceanic mantle and accumulated near the base of a convecting system for subsequent prolonged isolation [Christensen and Hofmann, 1994; Karato, 1997] to develop the isotopic characteristics suitable for FOZO or C. Its prevailing nature as a common source of oceanic basalts can be explained by the significant volume of subducted oceanic crust present in the mantle. However, the local trends toward FOZO or C, which are in general oblique to the ICs (Figures 3b and 4e), are minor structures within the IC space. Likewise, ICA shows no evidence for incorporation of what could represent a primordial mantle component or an early enriched reservoir into the observed depleted domain, which is consistent with 142Nd evidence [Boyet and Carlson, 2005]. The lack of a clear correlation between Pb-isotopic compositions and 3He/4He in oceanic basalts [Hanan and Graham, 1996] also suggests that the incorporation of primordial components is largely decoupled from the major mantle processes identified by ICA.
[27] Finally, the detected ICs call for a redefinition of the criteria used to identify the DUPAL anomaly. Hart [1984] defined three criteria on the basis of Sr- and Pb-isotopic ratios and their deviations from a Northern Hemisphere reference line. Although the overall distribution of the contours clearly shows the anomaly in the Southern Hemisphere, the three types of contours are not consistent with each other, especially in the Atlantic Ocean [see Hart, 1984, Figure 2]. In the IC space, the five isotopic ratios of Pb, Sr and Nd have been considered simultaneously, in which case a simpler and more consistent criterion can be obtained. As a result, as shown by Figure 6, the realm of the enriched region defined by a positive IC2 value is different from the DUPAL domain of Hart [1984]: the enriched signature distributes itself in the Northern Hemisphere, which is consistent with occurrence of a DUPAL signature along the Nansen-Gakkel Ridge [Mühe et al., 1993]. This could have an important implication on mantle dynamics: if the enriched region was initially confined to a distinct domain (e.g., because it represents a mantle domain contaminated by extensive Pangeatic subduction [Anderson, 1982; Zindler and Hart, 1986]), the disposition of the IC2 domain and the amplitude of the anomaly may provide unique information on the long-term mantle flow and material transport. Accounting for mantle isotopic variability in terms of the independent differentiation processes identified by ICA rather than by interactions among mantle geochemical end-members with unique compositions is therefore bridging the gap between geochemical observations and mantle dynamics.

5. Conclusions
[28] Independent component analysis has been applied to the isotopic compositional space of oceanic basalts. Two statistically independent components have been found, which characterize two independent features: one opposes mid-ocean ridge basalts to ocean island basalts, while the other maps geographically regional isotopic properties. The distribution of the data in the IC space demonstrates that the observed compositional space is created by the joint distribution of the two ICs, indicating that two distinct differentiation processes mutually overlap, rather than by interaction among the conventional mantle geochemical end-members with unique compositions. The geochemical characteristics of the two ICs oppose the variations due to melting from those caused by interaction of aqueous fluid with the mantle, both at mid-ocean ridges and at subduction zones. The ICs provide a new quantitative measure for describing the isotopic heterogeneity of the mantle. As a result, a new criterion is proposed for the definition of the DUPAL anomaly. It is shown that the DUPAL signature is present both in the Southern Hemisphere and the Northern Hemisphere, which possibly reflects a large-scale feature of the mantle flow.
Acknowledgments
[31] We thank Matt Miller and Yoshi Tatsumi for discussion and help and Dan McKenzie, John Rudge, Vincent Salters, and Bill White for constructive reviews. Janne Blichert-Toft obliged with a careful editing of the manuscript. F.A. would like to thank the Earthquake Research Institute for their generous invitation to visit the University of Tokyo and the Program SEDIT of the Institut National des Sciences de l'Univers for financial support.
Appendix A:: 204Pb Normalization Versus 206Pb Normalization
















