Elsevier

Chemical Geology

Volume 234, Issues 1–2, 30 October 2006, Pages 148-168
Chemical Geology

238U–230Th disequilibrium in recent basalts and dynamic melting beneath the Kenya rift

https://doi.org/10.1016/j.chemgeo.2006.05.002Get rights and content

Abstract

Trace element and U-series isotope analyses are presented for a suite of recent (< 10 ka) basalts from the axial portion of the Kenya rift. Samples from throughout the rift have LREE-enriched patterns with HREE > 10 × chondrite and the LREE between 60 and 200 × chondrite. REE fractionation is consistent with melting a garnet lherzolite source region with between 2% and 6% modal garnet. Other trace element ratios are distinct from OIB, notably Zr/Hf which ranges from 43 to 48, whilst at a given Zr content the Zr/Hf ratio is significantly greater than that found in OIB. (238U/232Th) range from 0.362 to 1.036, (230Th/232Th) from 0.503 to 1.109, with (230Th/238U) ranging from 0.783 to 2.966. All but two samples are in 230Th excess or in secular equilibrium. Samples with elevated (238U/232Th), also have Rb/Cs > 120, but unexceptional 208Pb/206Pb and hence κPb values. These samples have experienced U and Cs loss and are excluded from further consideration. Of the unaltered samples, all have (238U/232Th) generally lower than OIB, with maximum values of < 0.8, and some < 0.6. The maximum (230Th/238U) is 1.39, similar to OIB. Although none of the basalts has a primary composition, (230Th/238U) does not vary systematically with indices of fractionation, and comparison with evolved rocks from Kenya indicates that 238U–230Th disequilibrium in the basalts is not the product of fractionation and crustal residence, but a product of melt generation. The maximum (230Th/238U) that can be generated by batch melting, assuming a source mineralogy consistent with the REE variation is 1.05 and so the variation in (230Th/238U) is attributed to more complex models of melt generation and/or transport. Both dynamic melting and equilibrium porous flow suggest mantle upwelling rates of ≤ 2 cm year 1. It is suggested that the Kenya basalts represent melts derived from lithospheric mantle that has been thermally reactivated by and incorporated into the underlying (East African) mantle plume.

Introduction

Continental basaltic magmatism reveals a compositional diversity that is somewhat greater than that observed in the oceanic realm. While in part this relates to the interaction of mafic magmas with the more easily fusible parts of the continental crust, much compositional diversity has been attributed to magma sources located in the continental mantle lithosphere—that part of the mantle attached to the base of the continents, forming part of the plate structure that does not take part in mantle convection. Petrological investigations indicate that lithospheric melting occurs at slightly lower temperatures than melting in the asthenosphere because it is controlled by volatile-bearing phases, notably amphibole, phlogopite and, at greater depths, carbonate (e.g. Gallagher and Hawkesworth, 1992). Moreover, basalts from numerous CFB provinces and extensional continental regimes reveal compositional trends that are consistent with a pattern of early lithospheric melts followed by plume-related or asthenospheric magmas once the lithosphere has thinned (Perry et al., 1987, Fitton et al., 1991, Turner et al., 1996).

Physical models of continental magmatism that include lithospheric melting imply a period of conductive heating from an underlying mantle plume, leading to the generation and accumulation of melt within the mantle followed by extraction (Gallagher and Hawkesworth, 1992, Leeman and Harry, 1993). Alternatively, heating of the lithosphere may result in so-called thermal erosion during which lithospheric mantle is incorporated into the underlying asthenosphere or mantle plume where it is either removed from the system by convection or contributes to plume-related magmatism (Davies, 1994, Thoraval et al., 2006). These alternatives probably represent two extremes of a spectrum of processes but each implies a contrasting melting process. The first model is static and more akin to simple batch melting, whereas the second involves a dynamic system in which melt is extracted by compaction of a convecting matrix, similar to the predominant process operating beneath mid-ocean ridges and within mantle plumes. U-series isotopes have the potential to distinguish between these processes (e.g. McKenzie, 1985, Iwamori, 1994, Elliott, 1997, Zou and Zindler, 2000, Asmerom et al., 2000), and so inform physical models of plume–lithosphere interaction during continental extension and break-up.

Within the Kenya rift, mafic melts of variable composition have been generated over the past 35 Ma and reflect the interaction between the underlying mantle plume with the overlying lithosphere (e.g. Macdonald et al., 2001). Geophysical studies have revealed the detailed structure of the crust and mantle both along the rift and across the strike of the rift, and in particular, the presence of low velocity asthenospheric mantle with up to 6% partial melt beneath the axis of the Kenya rift (Green et al., 1991). Earlier investigations into the petrology of the Kenya basalts interpreted them as resulting from melting in a mantle plume (e.g. Latin et al., 1993). By contrast, more recent studies have demonstrated the strong control exerted by the lithosphere on the location, volume and composition of erupted magmas and have shown that the lithosphere acts as a major source of magma in many parts of the Kenya rift (e.g. Macdonald et al., 2001, Le Roex et al., 2001, Spath et al., 2001). The Kenya rift therefore offers an opportunity to investigate the processes that ultimately lead to the production of mafic melts from the mantle lithosphere. Are they produced by simple conductive heating of the lithosphere, or is the mantle lithosphere incorporated into a convecting, dynamic regime that has the physical properties of asthenosphere but the compositional characteristics of the mantle lithosphere?

Existing U-series data from the Kenya rift based on α-spectrometry reveal considerable 230Th excess over 238U (Black et al., 1998), implying a melting regime that extends into the garnet stability field, consistent with trace element, especially REE fractionation (Macdonald et al., 2001). However, the data do not readily distinguish between the different melting regimes and so the process whereby the lithosphere is remobilised during plume–lithosphere interaction and extension remains unclear. Here we present new mass spectrometric analyses of trace element abundances and (238U/230Th) disequilibrium from recent (< 10 ka) basalts from the Kenya rift that address these problems. They allow us to distinguish between batch and dynamic melting processes in the source regions of basalts with lithospheric origins, and emphasise the differences in source composition between the Kenya rift and plume-related magmatism generally.

Section snippets

Geological background and sample description

The African rift is one of the clearest currently active examples of continental magmatism related to extension above a mantle plume on Earth. The elevated topography and negative Bouguer gravity anomalies across the whole of East Africa (Ebinger et al., 1989), shallow and deep seismic tomography (Nyblade et al., 2000, Weeraratne et al., 2003) and the volume of magmas (Latin et al., 1993), testify to the presence of a thermal anomaly in the mantle that has been variously attributed to the

Analytical methods

Trace elements were determined by ICPMS analysis at the Open University, using an Agilent 7500s instrument fitted with a standard quartz spray chamber and a Babington nebuliser. 100 mg of sample were dissolved in 1 ml HF with 2 ml HNO3 in screw-top Teflon beakers overnight at a temperature of ∼ 120 °C. After further reaction with HNO3 and HCl to remove fluorides, samples were taken up in 3 ml concentrated HNO3 and the clear solutions diluted to 100 ml in 18 MΩ water to give a final solution in

Trace elements

Trace element analyses are tabulated in Table 2, together with published major element and Sr, Nd and Pb isotope analyses from earlier studies (Rogers et al., 2000, Macdonald et al., 2001) for completeness. All samples have LREE-enriched patterns with HREE > 10 × chondrite and the LREE between 60 and 200 × chondrite (Fig. 3). Small positive Eu anomalies reflect the possible effects of plagioclase accumulation, as do Sr/Nd ratios > 16. REE fractionation is clearly illustrated on a plot of La/Yb

Comparison with evolved magmas from the Kenya rift and crustal storage times

Two recent studies of variations in the behaviour of the U-series isotopes in felsic magmas within the Kenya rift have shown that, in contrast to their mafic counterparts, they have limited ranges in U–Th disequilibrium, and these are also illustrated in Fig. 7. The peralkaline rhyolites from the Greater Olkaria Volcanic Complex (GOVC) (Heumann and Davies, 2002) fall close to the equiline, whereas trachytes from Longonot (Rogers et al., 2004) define a near horizontal trend with (230Th/232Th)

Comparison with OIB and other continental mafic volcanic rocks

The Kenya basalt analyses are compared with similar data from selected OIB and continental mafic volcanics in Fig. 8, from which a number of features are apparent. Firstly, the Kenyan samples generally lie between OIB and continental volcanics, with intermediate (238U/232Th) ratios. Secondly, with two exceptions, all samples show an excess of 230Th over 238U although the maximum (230Th/238U) ratio is 1.39, no more extreme than values from OIB and MORB. Thirdly, the range of (238U/232Th) in the

Lithosphere in the melting regime

We have shown elsewhere that the radiogenic isotope characteristics of the basalts within the Kenya rift vary with the age of the underlying lithosphere (Rogers et al., 2000), and that critical aspects of the trace element composition of all Kenya basalts, e.g. the Zr/Hf, Nb/Ta ratios, are also different from those typical of OIB and not simply a function of melt fraction. These differences are not caused by crustal interaction as crustal samples tend to have low Zr/Hf and Nb/Ta ratios (David

Conclusions

Basalts from the Kenya rift result from melting of a lherzolite mantle with 2–6% garnet in the source region. Trace elements are distinct from OIB (notably low U/Th, high Nb/Ta and Zr/Hf ratios and low Zr contents), suggesting either an origin in the mantle lithosphere or that the mantle source has incorporated a lithospheric component that dominates the trace element and hence isotope characteristics of the erupted lavas. After screening for the effects of alteration and U mobility, U-series

Acknowledgements

The authors would like to thank Craig Lundstrom and Tanya Furman for their constructive reviews, Roberta Rudnick for similarly constructive editorial comments and David Peate for comments on an earlier draft and access to his compilation of MORB and OIB U-series data. Many thanks also to Andy Lloyd for the figures. U-series and trace element research at the Open University is funded by NERC as part of the Research Facilities Infra-structure and grant GR3/JREI/149 respectively. [RR]

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