Geology ReportsSearch

Geology topics

R. K. O’Nions

Publications and source records attributed to R. K. O’Nions.

6 recordsLinked to original sources

60 Myr records of major elements and Pb-Nd isotopes from hydrogenous ferromanganese crusts: Reconstruction of seawater paleochemistry

We compare the time series of major element geochemical and Pb- and Nd-isotopic composition obtained for seven hydrogenous ferromanganese crusts from the Atlantic, Indian, and Pacific Oceans which cover the last 60 Myr. Average crust growth rates and age-depth relationships were determined directly for the last about 10 Myr using 10Be/9Be profiles. In the absence of other information these were extrapolated to the base of the crusts assuming constant growth rates and constant initial 10Be/9Be ratios due to the lack of additional information. Co contents have also been used previously to estimate growth rates in Co-rich Pacific and Atlantic seamount crusts (Puteanus and Halbach, 1988). A comparison of 10Be/9Be- and Co-based dating of three Co-rich crusts supports the validity of this approach and confirms the earlier chronologies derived from extrapolated 10Be/9Be-based growth rates back to 60 Ma. Our data show that the flux of Co into Co-poor crusts has been considerably lower. The relationship between growth rate and Co content for the Co-poor crusts developed from these data is in good agreement with a previous study of a wider range of marine deposits (Manheim, 1986). The results suggest that the Co content provides detailed information on the growth history of ferromanganese crusts, particularly prior to 10-12 Ma where the 10Be-based method is not applicable. The distributions of Pb and Nd isotopes in the deep oceans over the last 60 Myr are expected to be controlled by two main factors: (a) variations of oceanic mixing patterns and flow paths of water masses with distinct isotopic signatures related to major paleogeographic changes and (b) variability of supply rates or provenance of detrital material delivered to the ocean, linked to climate change (glaciations) or major tectonic uplift. The major element profiles of crusts in this study show neither systematic features which are common to crusts with similar isotope records nor do they generally show coherent relationships to the isotope records within a single crust. Consequently, any interpretation of time series of major element concentrations of a single crust in terms of paleoceanographic variations must be considered with caution. This is because local processes appear to have dominated over more basin-wide paleoceanographic effects. In this study Co is the only element which shows a relationship to Pb and Nd isotopes in Pacific crusts. A possible link to changes of Pacific deep water properties associated with an enhanced northward advection of Antarctic bottom water from about 14 Ma is consistent with the Pb but not with the Nd isotopic results. The self-consistent profiles of the Pb and Nd isotopes suggest that postdepositional diagenetic processes in hydrogenous crusts, including phosphatization events, have been insignificant for particle reactive elements such as Pb, Be, and Nd. Isotope time series of Pb and Nd show no systematic relationships with major element contents of the crusts, which supports their use as tracers of paleo-seawater isotopic composition.

Geochimica et Cosmochimica Acta

Evolution of Nd and Pb isotopes in Central Pacific seawater from ferromanganese crusts

Hydrogenetic ferromanganese crusts incorporate elements from ambient seawater during their growth on seamounts. By analysing Nd, Pb and Be isotope profiles within crusts it is possible to reconstruct seawater tracer histories. Depth profiles of 10 Be/ 9 Be ratios in three Pacific ferromanganese crusts have been used to obtain growth rates which are between 1.4 and 3.8 mm/Ma. Nd and Pb isotopes provide intact records of isotopic variations in Pacific seawater over the last 20 Ma or more. There were only small changes in Pb isotope composition in the last 20 Ma. This indicates a constant Pb composition for the erosional sources and suggests further that erosional Nd inputs may have been uniform too. ε Nd values vary considerably with time and most probably reflect changes in ocean circulation. The ε Nd values of the crusts not only vary as a function of age but also as a function of water depth. From 25 to 0 Ma, crust VA13/2 from 4.8 km water depth has a similar pattern of ε Nd variation to the two shallower crusts from 1.8 and 2.3 km, but about 1.0 to 1.5 units more negative. This suggests that ε Nd stratification in Pacific seawater, as demonstrated for the present day, has been maintained for at least 20 Ma. Each crust shows a decrease in ε Nd from 3–5 Ma to the present, which is interpreted in terms of an increase in the NADW component present in the Pacific. From 10 to 3–5 Ma ago the crusts show an increase in ε Nd . This suggests a decreasing role for a deep water source with ε Nd less than circum-Pacific sources. In this regard the Panamanian gateway restriction from ∼ 10 Ma with final closure at 3–5 Ma may have played an important role in reducing access of Atlantic-derived Nd to the Pacific.

Earth and Planetary Science Letters

238U-234U-230Th disequilibrium in hydrogenous oceanic Fe-Mn crusts: Palaeoceanographic record or diagenetic alteration?

A detailed TIMS study of ( 234 U exc / 238 U), ( 230 Th/ 232 Th), and Th/U ratios have been performed on the outermost margin of ten hydrogenous Fe Mn crusts from the equatorial Pacific Ocean and west-central Indian Ocean.Th/U concentration ratios generally decrease from the crust's surface down to 0.5-1 mm depth and growth rates estimated by uranium and thorium isotope ratios are significantly different in Fe Mn crusts from the Peru Basin and the west-central Indian Ocean. Fe Mn crusts from the same geographical area define a single trend in plots of Ln( 234 U exc / 238 U) vs. Ln( 230 Th/ 232 Th) and Th/U ratios vs. age of the analysed fractions. Results suggest that (l) hydrogenous Fe Mn crusts remain closed-systems after formation, and consequently (2) the discrepancy observed between the 230 Th and 234U chronometers in Fe Mn crusts, and the variations of the Th/U ratios through the margin of FeMn crusts, are not due to redistribution of uranium and thorium isotopes after oxyhydroxide precipitation, but rather to temporal variations of both Th/U and initial thorium activity ratios recorded by the Fe Mn layers. Implications of these observations for determination of Fe Mn crust growth-rates are discussed. Variations of both Th/U and initial Th activity ratios in Fe Mn crusts might be related to changes in particle input to seawater and/or changes in ocean circulation during the last 150 ka.

Geochimica et Cosmochimica Acta

Global distribution of beryllium isotopes in deep ocean water as derived from Fe-Mn crusts

The direct measurement of the ratio of cosmogenic 10 Be ( T 1 2 = 1.5 Ma "> T12= 1.5 Ma ) to stable terrigenously sourced 9 Be in deep seawater or marine deposits can be used to trace water mass movements and to quantify the incorporation of trace metals into the deep sea. In this study a SIMS-based technique has been used to determine the 10 Be 9 Be "> 10Be9Be ratios of the outermost millimetre of hydrogenetic ferromanganese crusts from the worlds oceans. 10 Be 9 Be "> 10Be9Be ratios, time-corrected for radioactive decay of cosmogenic 10 Be using 234 U 238 U "> 234U238U , are in good agreement with AMS measurements of modern deep seawater. Ratios are relatively low in the North and equatorial Atlantic samples (0.4–0.5 × 10 −7 ). In the Southwest Atlantic ratios increase up to 1 × 10 −7 , they vary between 0.7 and 1.0 × 10 −7 in Indian Ocean samples, and have a near constant value of 1.1 ± 0.2 × 10 −7 for all Pacific samples. If the residence time of 10 Be ( τ 10 Be ) in deep water is constant globally, then the observed variations in 10 Be 9 Be "> 10Be9Be ratios could be caused by accumulation of 10 Be in deep water as it flows and ages along the conveyor, following a transient depletion upon its formation in the Northern Atlantic. In this view both 10 Be and 9 Be reach local steady-state concentration in Pacific deep water and the global τ10 Be ≌ 600 a ">≌ τ10Be≌ 600a . An alternative possibility is that the Be isotope abundances are controlled by local scavenging. For this scenario τ 10 Be would vary according to local particle concentration and would ≌ 600 a in the central Pacific, but τ10 Be ≌ 230 a ">≌ τ10Be≌ 230a in the Atlantic. Mass balance considerations indicate that hydrothermal additions of 9 Be to the oceans are negligible and that the dissolved riverine source is also small. Furthermore, aeolian dust input of 9 Be appears insufficient to provide the dissolved 9 Be inventory. The dissolution of only a small proportion (2%) of river-derived particulates could in principle supply the observed seawater 9 Be content. If true, ocean margins would be the sites for 9 Be addition. Due to the particle-reactive nature of Be, these would also be the primary sites of Be removal. A possible net result of horizontal water masses passing through these marginal areas might be a decrease in seawater 10 Be 9 Be "> 10Be9Be , and establishment of a relatively constant 9 Be concentration. As τ 10 Be (∼ 600 a) is less than the apparent age of deep water in the Pacific (∼ 1500 a), the Pacific record of 10 Be 9 Be "> 10Be9Be is not expected to show secular variations due to changes in deep-water flow, despite the large variations in 10 Be 9 Be "> 10Be9Be between different water masses. Because of this insensitivity to deep-water flow, however, it is suggested that the 10 Be 9 Be "> 10Be9Be ratio, determined in the authigenic phase of marine sediments or hydrogenetic precipitates, should be a suitable tool for monitoring changes in continental input or cosmic ray intensity on longer time scales.

Earth and Planetary Science Letters

Distribution and sources of pre-anthropogenic lead isotopes in deep ocean water from Fe-Mn crusts

The lead isotope composition of ocean water is not well constrained due to contamination by anthropogenic lead. Here the global distribution of lead isotopes in deep ocean water is presented as derived from dated (ca. 100 ka) surface layers of hydrogenetic Fe-Mn crusts. The results indicate that the radiogenic lead in North Atlantic deep water is probably supplied from the continents by river particulates, and that lead in Pacific deep water is similar to that characteristic of island and continental volcanic arcs. Despite a short residence time in deep water (80-100 a), the isotopes of lead appear to be exceedingly well mixed in the Pacific basin. There is no evidence for the import of North Atlantic deep water-derived lead into the Pacific ocean, nor into the North Indian Ocean. This implies that the short residence time of lead in deep water prohibits advection over such long distances. Consequently, any climate-induced changes in deep-water flow are not expected to result in major changes in the seawater Pb-isotope record of the Pacific Ocean.

Geochimica et Cosmochimica Acta

238U-234U-230Th chronometry of Fe-Mn crusts: Growth processes and recovery of thorium isotopic ratios of seawater

Comparison of ( ( 234 U)excess ( 238 U ) "> 234 U) excess ⁄ ( 238 U) and ( ( 230 Th 232 Th "> 230 Th ⁄ 232 Th ) activity ratios in oceanic Fe-Mn deposits provides a method for assessing the closed-system behaviour of 238 U- 234 U- 230 Th, as well as variations in the initial uranium and thorium isotopic ratios of the precipitated metal oxides. This approach is illustrated using a Fe-Mn crust from Lotab seamount (Marshall Islands, west equatorial Pacific). Here we report uranium and thorium isotopic compositions in five subsamples from the surface of one large 5 cm diameter botryoid of this crust, and from two depth profiles of the outermost rim of the same botryoid. The decrease of ( ( 234 U)excess ( 238 U ) "> 234 U) excess ⁄ ( 238 U) and ( ( 230 Th 232 Th "> 230 Th ⁄ 232 Th ) activity ratio with depth in the two profiles gives mean growth rates, for the last 150 ka, of 7.8 ± 2 mm/Ma and 6.6 ± 1 mm/Ma, respectively. All data points (surface and core samples) but one, define a linear correlation in the Ln ( 230 Th 232 Th − Ln ( 234 U)excess ( 238 U ) "> Ln ( ( 230 Th 232 Th "> 230 Th ⁄ 232 Th ) −Ln[ ( ( 234 U)excess ( 238 U ) "> 234 U) excess ⁄ ( 238 U) ] diagram. This correlation indicates that for all points the U-Th system remained closed after the Fe-Mn layer precipitated, and that the different samples possessed the same initial Uranium and thorium isotope ratios. Furthermore, these results show that the preserved surface of this Fe-Mn crust may not be the present-day growth surface, and that the thorium and uranium isotopic ratios of seawater in west equatorial Pacific have not changed during the past 150 ka. The initial thorium activity ratio is estimated from the correlation obtained between Ln ( 230 Th 232 Th − Ln ( 234 U)excess ( 238 U ) "> Ln ( ( 230 Th 232 Th "> 230 Th ⁄ 232 Th ) −Ln Ln ( 230 Th 232 Th − Ln ( 234 U)excess ( 238 U ) ">[ ( ( 234 U)excess ( 238 U ) "> 234 U) excess ⁄ ( 238 U) ] .

Lotab Seamount, Pacific Ocean