Was the Late Paleocene-Early Eocene Hot Because Earth Was Flat? An Ocean Lithium Isotope View of Mountain Building, Continental Weathering, Carbon Dioxide, and Earth's Cenozoic Clima

Hothouse climates in Earth’s geologic past, such as the Eocene epoch, \ud are thought to have been caused by the release of large amounts of carbon dioxide \ud and/or methane, which had been stored as carbon in biogenic gases and organic \ud matter in sediments, to the ocean-atmosphere system. However, to avoid runaway \ud temperatures, there must be long-term negative feedbacks that consume CO 2 on \ud time scales longer than the ~ 100,000 years generally ascribed to ocean uptake of \ud CO 2 and burial of marine organic carbon. Here, we argue that continental chemical \ud weathering of silicate rocks, the ultimate long-term (multi-million year) sink for \ud CO 2 , must have been almost dormant during the late Paleocene and early Eocene, \ud allowing buildup of atmospheric CO 2 to levels exceeding 1,000 ppm. This reduction \ud in the strength of the CO 2 sink was the result of minimal global tectonic uplift of \ud silicate rocks that did not produce mountains susceptible to physical and chemical \ud weathering, an inversion of the Uplift-Weathering Hypothesis. There is lack of \ud terrestrial evidence for absence of uplift; however, the δ 7 Li chemistry of the Paleogene \ud ocean indicates that continental relief during this period of the Early Cenozoic was \ud one of peneplained (flat) continents characterized by high chemical weathering \ud intensity and slow physical and chemical weathering rates, yielding low river fluxes \ud of suspended solids, dissolved cations, and clays delivered to the sea. Only upon \ud re-initiation of mountain building in the Oligocene-Miocene (Himalayas, Andes, \ud Rockies) and drifting of these continental blocks to low-latitude locations near the \ud Inter-Tropical Convergence Zone and monsoonal climate belts did continental \ud weathering take on modern characteristics of rivers with high suspended loads and \ud incongruent weathering, with much of the cations released during weathering being \ud sequestered into secondary clay minerals. The δ 7 Li record of the Cenozoic ocean \ud provides another piece of circumstantial evidence in support of the Late Cenozoic \ud Uplift-Weathering Hypothesis

Investigating the effects of growth rate and temperature on the B/Ca ratio and δ11B during inorganic calcite formation

To deconvolve the effect of growth rate and temperature on the boron partitioning into calcite and its isotope fractionation, seeded calcite precipitation experiments were performed at a constant temperature and various growth rates and at a constant growth rate and various temperatures. We show that boron partitioning increases with increasing growth rate and decreases with increasing temperature. The B isotope fractionation between calcite and B(OH)4− increases with increasing growth rate favoring the lighter B isotope for incorporation into calcite whereas no effect of temperature was observed within the temperature range investigated (12 °C to 32 °C). At the lowest temperature and growth rate δ11B of the calcite almost equals that of B(OH)4− in solution. Applying the surface entrapment model (SEMO) of Watson and Liang (1995) to our data, we demonstrate that the observed effects of temperature and growth rate on B concentration can be explained by processes in the near surface layer of the calcite crystal

High-precision determination of lithium and magnesium isotopes utilising single column separation and multi-collector inductively coupled plasma mass spectrometry

Li and Mg isotopes are increasingly used as a combined tool within the geosciences. However, established methods require separate sample purification protocols utilising several column separation procedures. This study presents a single-step cation-exchange method for quantitative separation of trace levels of Li and Mg from multiple sample matrices

Abrupt changes in the southern extent of North Atlantic Deep Water during Dansgaard–Oeschger events

The glacial climate system transitioned rapidly between cold (stadial) and warm (interstadial) conditions in the Northern Hemisphere. This variability, referred to as Dansgaard–Oeschger variability, is widely believed to arise from perturbations of the Atlantic Meridional Overturning Circulation. Evidence for such changes during the longer Heinrich stadials has been identified, but direct evidence for overturning circulation changes during Dansgaard–Oeschger events has proven elusive. Here we reconstruct bottom water [CO32−] variability from B/Ca ratios of benthic foraminifera and indicators of sedimentary dissolution, and use these reconstructions to infer the flow of northern-sourced deep water to the deep central sub-Antarctic Atlantic Ocean. We find that nearly every Dansgaard–Oeschger interstadial is accompanied by a rapid incursion of North Atlantic Deep Water into the deep South Atlantic. Based on these results and transient climate model simulations, we conclude that North Atlantic stadial–interstadial climate variability was associated with significant Atlantic overturning circulation changes that were rapidly transmitted across the Atlantic. However, by demonstrating the persistent role of Atlantic overturning circulation changes in past abrupt climate variability, our reconstructions of carbonate chemistry further indicate that the carbon cycle response to abrupt climate change was not a simple function of North Atlantic overturning

High-precision determination of lithium and magnesium isotopes utilising single column separation and multi-collector inductively coupled plasma mass spectrometry.

RATIONALE: Li and Mg isotopes are increasingly used as a combined tool within the geosciences. However, established methods require separate sample purification protocols utilising several column separation procedures. This study presents a single-step cation-exchange method for quantitative separation of trace levels of Li and Mg from multiple sample matrices. METHODS: The column method utilises the macro-porous AGMP-50 resin and a high-aspect ratio column, allowing quantitative separation of Li and Mg from natural waters, sediments, rocks and carbonate matrices following the same elution protocol. High-precision isotope determination was conducted by multi-collector inductively coupled plasma mass spectrometry (MC-ICPMS) on the Thermo Scientific™ NEPTUNE Plus™ fitted with 1013  Ω amplifiers which allow accurate and precise measurements at ion beams ≤0.51 V. RESULTS: Sub-nanogram Li samples (0.3-0.5 ng) were regularly separated (yielding Mg masses of 1-70 μg) using the presented column method. The total sample consumption during isotopic analysis is <0.5 ng Li and <115 ng Mg with long-term external 2σ precisions of ±0.39‰ for δ7 Li and ±0.07‰ for δ26 Mg. The results for geological reference standards and seawater analysed by our method are in excellent agreement with published values despite the order of magnitude lower sample consumption. CONCLUSIONS: The possibility of eluting small sample masses and the low analytical sample consumption make this method ideal for samples of limited mass or low Li concentration, such as foraminifera, mineral separates or dilute river waters

Antarctic Intermediate Water properties since 400 ka recorded in infaunal (Uvigerina peregrina) and epifaunal (Planulina wuellerstorfi) benthic foraminifera

Reconstruction of intermediate water properties is important for understanding feedbacks within the ocean-climate system, particularly since these water masses are capable of driving high–low latitude teleconnections. Nevertheless, information about intermediate water mass evolution through the late Pleistocene remains limited. This paper examines changes in Antarctic Intermediate Water (AAIW), the most extensive intermediate water mass in the modern ocean through the last 400 kyr using the stable isotopic composition (δ18O and δ13C) and trace element concentration (Mg/Ca and B/Ca) of two benthic foraminiferal species from the same samples: epifaunal Planulina wuellerstorfi and infaunal Uvigerina peregrina. Our results confirm that the most reasonable estimates of AAIW temperature and Δ[CO2−3] are generated by Mg/CaU. peregrina and B/CaP. wuellerstorfi, respectively. We present a 400 kyr record of intermediate water temperature and Δ[CO2−3] from a sediment core from the Southwest Pacific (DSDP site 593; 40°30′S, 167°41′E, 1068 m water depth), which lies within the core of modern AAIW. Our results suggest that a combination of geochemical analyses on both infaunal and epifaunal benthic foraminiferal species yields important information about this critical water mass through the late Pleistocene. When combined with two nearby records of water properties from deeper depths, our data demonstrate that during interglacial stages of the late Pleistocene, AAIW and Circumpolar Deep Water (CPDW) have more similar water mass properties (temperature and δ13C), while glacial stages are typified by dissimilar properties between AAIW and CPDW in the Southwest Pacific. Our new Δ[CO2−3] record shows short time-scale variations, but a lack of coherent glacial–interglacial variability indicating that large quantities of carbon were not stored in intermediate waters during recent glacial periods

Li Partitioning Into Coccoliths of Emiliania huxleyi : Evaluating the General Role of “Vital Effects” in Explaining Element Partitioning in Biogenic Carbonates

Emiliania huxleyi cells were grown in artificial seawater of different Li and Ca concentrations and coccolith Li/Ca ratios determined. Coccolith Li/Ca ratios were positively correlated to seawater Li/Ca ratios only if the seawater Li concentration was changed, not if the seawater Ca concentration was changed. This Li partitioning pattern of E. huxleyi was previously also observed in the benthic foraminifer Amphistegina lessonii and inorganically precipitated calcite. We argue that Li partitioning in both E. huxleyi and A. lessonii is dominated by a coupled transmembrane transport of Li and Ca from seawater to the site of calcification. We present a refined version of a recently proposed transmembrane transport model for Li and Ca. The model assumes that Li and Ca enter the cell via Ca channels, the Li flux being dependent on the Ca flux. While the original model features a linear function to describe the experimental data, our refined version uses a power function, changing the stoichiometry of Li and Ca. The version presented here accurately predicts the observed dependence of DLi on seawater Li/Ca ratios. Our data demonstrate that minor element partitioning in calcifying organisms is partly mediated by biological processes even if the partitioning behavior of the calcifying organism is indistinguishable from that of inorganically precipitated calcium carbonate

Decoupled carbonate chemistry controls on the incorporation of boron into Orbulina universa

In order to fully constrain paleo-carbonate systems, proxies for two out of seven parameters, plus temperature and salinity, are required. The boron isotopic composition (δ11B) of planktonic foraminifera shells is a powerful tool for reconstructing changes in past surface ocean pH. As B(OH)4− is substituted into the biogenic calcite lattice in place of CO32−, and both borate and carbonate ions are more abundant at higher pH, it was suggested early on that B ∕ Ca ratios in biogenic calcite may serve as a proxy for [CO32−]. Although several recent studies have shown that a direct connection of B ∕ Ca to carbonate system parameters may be masked by other environmental factors in the field, there is ample evidence for a mechanistic relationship between B ∕ Ca and carbonate system parameters. Here, we focus on investigating the primary relationship to develop a mechanistic understanding of boron uptake. Differentiating between the effects of pH and [CO32−] is problematic, as they co-vary closely in natural systems, so the major control on boron incorporation remains unclear. To deconvolve the effects of pH and [CO32−] and to investigate their impact on the B ∕ Ca ratio and δ11B, we conducted culture experiments with the planktonic foraminifer Orbulina universa in manipulated culture media: constant pH (8.05), but changing [CO32−] (238, 286 and 534 µmol kg−1 CO32−) and at constant [CO32−] (276 ± 19.5 µmol kg−1) and varying pH (7.7, 7.9 and 8.05). Measurements of the isotopic composition of boron and the B ∕ Ca ratio were performed simultaneously using a femtosecond laser ablation system coupled to a MC-ICP-MS (multiple-collector inductively coupled plasma mass spectrometer). Our results show that, as expected, δ11B is controlled by pH but it is also modulated by [CO32−]. On the other hand, the B ∕ Ca ratio is driven by [HCO3−], independently of pH. This suggests that B ∕ Ca ratios in foraminiferal calcite can possibly be used as a second, independent, proxy for complete paleo-carbonate system reconstructions. This is discussed in light of recent literature demonstrating that the primary relationship between B ∕ Ca and [HCO3−] can be obscured by other environmental parameters

Diffusive processes in aqueous glass dissolution

Abstract: High level nuclear waste is often immobilised in a borosilicate glass for disposal. However, this glass corrodes in contact with aqueous solutions. To predict radionuclide releases from wasteforms, their dissolution mechanisms must be understood. Understanding glass dissolution mechanisms presents a challenge across numerous other disciplines and many glass dissolution models still remain conflicted. Here we show that diffusion was a significant process during the later stages of dissolution of a simplified waste glass but was not evidenced during the initial stages of dissolution. The absence of measurable isotopic fractionation in solution initially supports models of congruent dissolution. However, the solution becoming isotopically lighter at later times evidences diffusive isotopic fractionation and opposes models that exclude diffusive transport as a significant mechanism. The periodically sampled isotopic methodologies outlined here provide an additional dimension with which to understand glass dissolution mechanisms beyond the usual measurement of solution concentrations and, post-process, nano-scale analysis of the altered glass

ANALYSIS OF YELLOW RIVER MIXING PROCESSES INTO THE BO HAI SEA VIA BARIUM AND RADIUM ISOTOPES

The mixing rate of dissolved substances from the Yellow River into the Bohai Sea is an important parameter in understanding the nutrient input to the coastal ocean. We present an assessment of the mixing rates under different discharge patterns using naturally-occurring short-lived radium isotopes. Radium and salinity measurements were collected along transects through the Yellow River salinity gradient and into the coastal Bohai Sea during three field expeditions. Mixing rates varied between 5 and 18 km2/day and were strongly dependent on river discharge. The highest mixing rates are found just after periods of high discharge, while the lowest mixing rates occurred after periods of relatively low discharge