Modern Ocean Research Articles

Stable Chromium Isotope Fractionation During the Alteration of Abyssal Peridotite: Implications for Marine Chromium Isotope Mass Balance

AbstractThe stable chromium isotope system has been widely used as a redox proxy to reconstruct the oxygenation history of ocean atmosphere systems. However, the Cr isotope mass balance in modern oceans (i.e., inputs and outputs) remains poorly constrained. To investigate the influence of seawater‐peridotite reaction on the global marine Cr isotope mass balance, we report high‐precision Cr isotope data (δ53Cr) on a series of fresh and altered abyssal peridotites from the Gakkel Ridge and the Southwest Indian Ridge (SWIR). The least altered peridotites give a δ53Cr value of −0.08 ± 0.06‰ (2SD, n = 4) for the oceanic mantle which is consistent with the established δ53Cr of the Bulk Silicate Earth. Compared to fresh peridotites, a subset of altered peridotites exhibit a loss of isotopically light Cr with relatively positive δ53Cr values (up to 0.04‰). These altered peridotites are characterized by significant Cr loss and likely have been subject to serpentinization. By contrast, seafloor weathering has limited influence on the Cr concentrations and isotopic compositions of the altered peridotites. Monte Carlo (MC) simulations of marine alteration suggest a net Cr flux into seawater from altered abyssal peridotites of ∼3.5 × 108 mol/yr, which is on the same order of magnitude as the riverine input flux of 108–109 mol/yr. Furthermore, the MC results suggest that the peridotite‐sourced net Cr flux has a negative δ53Cr signature (−0.33 ± 0.21‰, 2SD). Thus, seawater‐peridotite interactions must be considered when evaluating the modern oceanic Cr isotope mass balance.

Distributions of zirconium, hafnium, and niobium in the Indian Ocean: Influence of lithogenic sources on incompatible elements

Zirconium (Zr), hafnium (Hf), and niobium (Nb) are incompatible elements concentrated on the granitic continent. They are trace elements at the pmol/kg level in seawater and are considered potential tracers for water masses. However, data on the distribution of the three elements in modern oceans are limited, particularly in the Indian Ocean. Here, we report the first basin-scale sectional distributions of the three elements at 11 stations from 62°S to 17°N in the Indian Ocean and Indian sector of the Southern Ocean. Unfiltered and filtered seawater samples were stored in low-density polyethylene (LDPE) bottles for approximately 12 years and used to determine the concentrations of the total dissolvable (td) and dissolved (d) fractions, respectively. We found that the absorption percentages on the bottle wall were <10% for Zr, Hf, and Nb. The concentration ranges of dZr, dHf, and dNb in the Indian Ocean and Indian sector of the Southern Ocean were 8–348, 0.06–1.06, and 1.3–4.3 pmol/kg, respectively. The labile particulate (lp) concentration was obtained as the difference between td and d, which was less than the detection limit in most samples. The concentrations of dZr, dHf, and dNb in surface water were high in the Bay of Bengal and Arabian Sea, and the concentrations of Zr and Hf in the deep waters of the Indian Ocean were higher than those in the deep waters of the North Pacific Ocean in a similar manner with dAl. These results indicate that the Indian Ocean has strong influences of lithogenic sources for Al, Zr, and Hf. The dZr/dHf mole ratio characterized water masses in the Indian Ocean and increased in the following order: Atlantic Ocean < Indian Ocean < Pacific Ocean due to the preferential removal of dHf over dZr during thermohaline circulation and the local input of dZr and dHf in the Indian Ocean. Thus, we propose that the dZr/dHf ratio is a potential tracer for global ocean circulation.

Early diagenetic control on the enrichment and mobilization of rare earth elements and transition metals in buried ferromanganese crust

Ferromanganese crusts on seamounts represent a major reservoir of various critical metal elements (e.g., rare earth elements and transition metals) and hold substantial economic value. However, current research primarily focuses on crusts that are exposed to seawater, and little is known about the resource potential of buried crusts in sediments and the impact of early diagenesis on buried crusts. Here, we present in-situ high-resolution major and trace element analyses of a buried crust from the western Pacific Ocean to unravel how rare earth elements and transition metals are enriched and mobilized as burial. The elemental profiles of the buried crust indicate that as the crust is buried, dissolved nickel (Ni) and copper (Cu) are gradually released from it into the porewater. Manganese and cobalt (Co) contents of the buried crust remain relatively constant, while rare earth elements are incorporated into the buried crust. Collectively, the early diagenesis leads to the release of Ni and Cu into the porewater, whereas it facilitates the fixation of rare earth elements within the buried crust. Given the widespread distribution of buried crusts in modern oceans, they represent a potential resource for future economic extraction of critical metals, particularly rare earth elements and Co.

Productivity and organic carbon loading control uranium isotope behavior in ancient reducing settings: Implications for the paleoredox proxy

Uranium isotopes in ancient sedimentary rocks have emerged as a powerful proxy for the oxygenation history of Earth surface environments. Proper quantitative interpretation of δ238U data hinges, however, on an understanding of isotopic fractionation associated with uranium removal to sediments under different redox conditions. Whereas oxygenated environments are plentiful in the modern ocean, euxinic settings are scarce today, and persistently ferruginous settings are not a feature in the modern ocean, leaving lakes as our best analogs for iron-rich waters. These challenges to studying δ238U behavior under contemporaneous oxic, euxinic (sulfidic), and ferruginous (iron-rich) marine conditions limit our ability to apply the isotope proxy to ancient oceans. Here, we present δ238U data from five coeval cores through the Lower Mississippian Sunbury Shale of the semi-restricted Appalachian Basin (North America), which were deposited across a strong redox gradient from intermittently oxic conditions proximal to the Catskill Delta, to ferruginous conditions in the central basin axis and euxinic conditions along the basin-bounding Cumberland Sill. Overall, we find that both euxinic and ferruginous environments are capable of imparting high degrees of uranium isotope fractionation and that δ238U values covary more strongly with total organic carbon (TOC) and trace metal abundances than they do with the presence of euxinic versus ferruginous conditions. We suggest uranium sorption or incorporation into sinking organic matter in the water column as a mechanism for generating positive covariation between δ238U and TOC, particularly at lower TOC concentrations. We also compare our δ238U data to broadly coeval carbonates from Nevada, which can be used to estimate Early Mississippian seawater δ238U values. We find that Sunbury Shale cores deposited under stably anoxic conditions (both euxinic and ferruginous) and under consistently brackish salinities away from freshwater sources record an increasing δ238U trend through time that loosely mirrors the record for carbonates (and thus estimates for seawater) with an offset of ∼0.4‰ to 1.1‰, depending on the inferred offset between carbonate and seawater. In contrast, cores deposited close to the Catskill Delta and in a shallow oceanic-restricted basin transition across the Cumberland Sill record a decreasing δ238U trend through time, opposite the inferred seawater trend and suggestive of entirely local controls on δ238U values. Ultimately, these data suggest that highly productive environments with high rates of organic carbon loading can exert a strong control on the global δ238U mass balance regardless of whether euxinic or ferruginous conditions are present. These results necessitate a partial reassessment of the processes controlling δ238U variability in seawater and sedimentary rocks through Earth history.

Coupling of nitrogen biogeochemical cycling and phytoplankton community structure before and after the Late Ordovician mass extinction in South China

The Ordovician–Silurian transition (OST) is a crucial geological interval in Earth history, coinciding with the first of the ‘Big Five’ Phanerozoic mass extinction events (ca. 445 Ma). In addition to the dramatic loss of biodiversity, significant environmental change course such as redox conditions and nutrient availability have been the focus of debate. Previous studies have used isotopes of nitrogen (N) to reconstruct the redox evolution of the paleo-ocean and have identified biological nitrogen fixation as the main mode of nitrogen cycling during the OST. However, low δ15N values, ranging from −2‰ to +1‰, possibly correspond to four different redox conditions. The precise roles of these redox conditions and the spatial distributions of phytoplankton communities under different nitrogen cycles remain elusive. Here we present high-resolution nitrogen isotope, carbon isotope and lipid biomarker datasets from two drilled sections located on a submerged high of the Yangtze Basin to unravel the coupling between nitrogen biogeochemical cycling and phytoplankton community structure across the OST. The results suggest that there was a dominantly biological nitrogen fixation with local aerobic nitrogen cycling in the Yangtze Sea, and the nitrate inventory during the OST was smaller than that in the modern ocean. Particularly, before the Late Ordovician mass extinction (LOME), N-fixing cyanobacteria were likely extensively developed in the photic zone, while eukaryotic algae were limited. After the LOME, sea levels rose and the chemocline was higher than before the LOME. There was probably some NO3− that did not undergo denitrification in the surface ocean, favoring the development of eukaryotic algae. The ecological diversification from prokaryotic cyanobacteria to eukaryotic phytoplankton to eukaryotic zooplankton is likely to be a response to the enhanced biological pump, which generates positive feedbacks among the evolution of eukaryotic phytoplankton, organic matter enrichment, ocean oxygenation and atmospheric oxygen levels.

Sedimentary environment and benthic oxygenation history of the Upper Cretaceous Austin Chalk Group, south Texas: An integrated ichnological, sedimentological and geochemical approach

ABSTRACTOxygen concentration in the ocean is vital for sustaining marine ecosystems. While the potential impacts of deoxygenation on modern oceans are hard to predict, lessons can be learned from better characterizing past geological intervals formed under a greenhouse climate. The greenhouse Cretaceous containing several oceanic anoxic events characterized by widespread oxygen‐deficient water is ideal in this regard. The Austin Chalk Group in south Texas (USA) shows organic‐rich intervals that can be linked to oxygen depletion in the ocean, but the exact bottom water oxygenation conditions have not been estimated. This study aims to reconstruct both sediment interstitial and bottom water oxygenation history during Austin Chalk Group deposition by integrating detailed ichnological, sedimentological and geochemical (X‐ray fluorescence and X‐ray diffraction) analyses, thereby providing a consistent model that may be applicable across a range of marine shelf settings. The 141.12 m Gise #1 core contains a continuous record of the Austin Chalk Group, providing an opportunity for unravelling oxygenation and deoxygenation events. Whereas the anaerobic–exaerobic deposits are essentially nonbioturbated, four oxygen‐related ichnocoenoses are defined, further refining the transition of aerobic to dysaerobic conditions in the sediment interstitial water. Omission surfaces and glauconitic grains, products of current‐induced scouring and condensation, suggest sporadic high‐energy events in the Austin Chalk Group ramp that drove elevated terrestrial inputs. Geochemical data further help to identify anoxic bottom water conditions within the anaerobic facies. Additionally, the lowermost part of the Austin Chalk Group illustrates redox cycles, whereas dilution events characterized by elevated terrestrial input are identified throughout the rest of the Austin Chalk Group. The evolution of oxygenation levels in sediment interstitial water and bottom water disputes the existence of a long‐lasting oxygen‐deficient sea in south Texas. The refined depositional model may be applicable to coeval shelfal settings. Moreover, the results provide insights into variable, evolving palaeoclimatic and palaeoceanographic conditions of the greenhouse Late Cretaceous.

Ocean Oxygen, Preformed Nutrients, and the Cause of the Lower Carbon Dioxide Concentration in the Atmosphere of the Last Glacial Maximum

AbstractAll else equal, if the ocean's “biological [carbon] pump” strengthens, the dissolved oxygen (O2) content of the ocean interior declines. Confidence is now high that the ocean interior as a whole contained less oxygen during the ice ages. This is strong evidence that the ocean's biological pump stored more carbon in the ocean interior during the ice ages, providing the core of an explanation for the lower atmospheric carbon dioxide (CO2) concentrations of the ice ages. Vollmer et al. (2022, https://doi.org/10.1029/2021PA004339) combine proxies for the oxygen and nutrient content of bottom waters to show that the ocean nutrient reservoir was more completely harnessed by the biological pump during the Last Glacial Maximum, with an increase in the proportion of dissolved nutrients in the ocean interior that were “regenerated” (transported as sinking organic matter from the ocean surface to the interior) rather than “preformed” (transported to the interior as dissolved nutrients by ocean circulation). This points to changes in the Southern Ocean, the dominant source of preformed nutrients in the modern ocean, with an apparent additional contribution from a decline in the preformed nutrient content of North Atlantic‐formed interior water. Vollmer et al. also find a lack of LGM‐to‐Holocene difference in the preformed 13C/12C ratio of dissolved inorganic carbon. This finding may allow future studies to resolve which of the proposed Southern Ocean mechanisms was most responsible for enhanced ocean CO2 storage during the ice ages: (a) coupled changes in ocean circulation and biological productivity, or (b) physical limitations on air‐sea gas exchange.

Sulfur geochemistry of the Salitre Formation phosphorites: Implications for the role of microbial ecology and sulfur cycling in phosphogenesis on an Ediacaran carbonate platform

The distribution and activity of polyphosphate-accumulating sulfide oxidizing bacteria within marine sediments control the spatial distribution of sedimentary phosphorite formation in the modern ocean. In modern phosphogenetic settings, the concerted effect of microbial sulfide oxidation and microbial sulfate reduction in sediment pore waters is preserved in the sulfur isotope composition of trace sulfate in authigenic and early-stage diagenetic carbonate cements and phosphatic cements, as well as that of authigenic pyrite. If such variations in microbial sulfur metabolism controlled the spatial distribution of early phosphate mineralization in the geologic past, then one would expect to find differences between the sulfur isotope composition of cement-forming minerals in phosphatic and non-phosphatic facies of ancient sedimentary phosphate deposits. Here, we present paired measurements of the sulfur isotope composition of structural sulfate and structural sulfide in pore cements from co-occurring phosphatic and non-phosphatic facies of the Ediacaran Salitre Formation (Northeastern Brazil). The difference between δ34S of trace structural sulfate in carbonate cements (CAS) or phosphate cements (PAS) and δ34S of structural sulfide in pyrite or chromium-reducible sulfur (CRS), defined as Δ34S, provides a constraint on sulfur cycling within the pore waters from which the cements precipitated. In carbonate-cemented textures of the Salitre Formation, Δ34S = 12 to 31 ‰. In phosphate-cemented textures, however, PAS and pyrite crystals had more similar sulfur isotope compositions: Δ34S = −5–12 ‰. These values support the hypothesis that microbial sulfide oxidation was more prevalent in pore waters where phosphate mineralization occurred compared to pore waters where carbonate mineralization occurred – suggesting that microbial sulfide oxidation may have enabled the formation of sedimentary phosphorite on an Ediacaran carbonate platform, just as in modern phosphogenetic sites.

Degradation and accumulation of organic matter in euxinic surface sediments

The impact of oxygen on the preservation of organic matter in marine surface sediments is still controversial. We revisited this long-standing debate by determining the burial efficiency of sedimentary organic matter in the Black Sea, the largest anoxic and euxinic basin in the modern ocean. Surface sediments were sampled in the Danube paleodelta on the northwestern margin of the Black Sea at 420–1550 m water depth. Steady-state modeling of solid species (particulate organic carbon and nitrogen) and solutes (ammonium, sulfate, and total alkalinity) in sediments was performed to quantify rates of mass accumulation, particulate organic matter (POM) degradation, and POM burial. We develop a novel analytical model to quantify these rates applying an inverse modelling approach to down core data accounting for molecular diffusion, sediment burial and compaction. Our model results indicate that 56.7 ± 6.6 % of the particulate organic matter deposited in the study area is not degraded in surface sediments but accumulates below 10 cm sediment depth. This burial efficiency is substantially higher than those previously derived for seafloor areas underlying oxygenated bottom waters. Hence, our study confirms previous studies showing that euxinic bottom water conditions promote the preservation of particulate organic matter in marine sediments.

A timeline of bacterial and archaeal diversification in the ocean

Microbial plankton play a central role in marine biogeochemical cycles, but the timing in which abundant lineages diversified into ocean environments remains unclear. Here, we reconstructed the timeline in which major clades of bacteria and archaea colonized the ocean using a high-resolution benchmarked phylogenetic tree that allows for simultaneous and direct comparison of the ages of multiple divergent lineages. Our findings show that the diversification of the most prevalent marine clades spans throughout a period of 2.2 Ga, with most clades colonizing the ocean during the last 800 million years. The oldest clades – SAR202, SAR324, Ca. Marinimicrobia, and Marine Group II – diversified around the time of the Great Oxidation Event, during which oxygen concentration increased but remained at microaerophilic levels throughout the Mid-Proterozoic, consistent with the prevalence of some clades within these groups in oxygen minimum zones today. We found the diversification of the prevalent heterotrophic marine clades SAR11, SAR116, SAR92, SAR86, and Roseobacter as well as the Marine Group I to occur near to the Neoproterozoic Oxygenation Event (0.8–0.4 Ga). The diversification of these clades is concomitant with an overall increase of oxygen and nutrients in the ocean at this time, as well as the diversification of eukaryotic algae, consistent with the previous hypothesis that the diversification of heterotrophic bacteria is linked to the emergence of large eukaryotic phytoplankton. The youngest clades correspond to the widespread phototrophic clades Prochlorococcus, Synechococcus, and Crocosphaera, whose diversification happened after the Phanerozoic Oxidation Event (0.45–0.4 Ga), in which oxygen concentrations had already reached their modern levels in the atmosphere and the ocean. Our work clarifies the timing at which abundant lineages of bacteria and archaea colonized the ocean, thereby providing key insights into the evolutionary history of lineages that comprise the majority of prokaryotic biomass in the modern ocean.

A timeline of bacterial and archaeal diversification in the ocean.

Microbial plankton play a central role in marine biogeochemical cycles, but the timing in which abundant lineages diversified into ocean environments remains unclear. Here, we reconstructed the timeline in which major clades of bacteria and archaea colonized the ocean using a high-resolution benchmarked phylogenetic tree that allows for simultaneous and direct comparison of the ages of multiple divergent lineages. Our findings show that the diversification of the most prevalent marine clades spans throughout a period of 2.2 Ga, with most clades colonizing the ocean during the last 800 million years. The oldest clades - SAR202, SAR324, Ca. Marinimicrobia, and Marine Group II - diversified around the time of the Great Oxidation Event, during which oxygen concentration increased but remained at microaerophilic levels throughout the Mid-Proterozoic, consistent with the prevalence of some clades within these groups in oxygen minimum zones today. We found the diversification of the prevalent heterotrophic marine clades SAR11, SAR116, SAR92, SAR86, and Roseobacter as well as the Marine Group I to occur near to the Neoproterozoic Oxygenation Event (0.8-0.4 Ga). The diversification of these clades is concomitant with an overall increase of oxygen and nutrients in the ocean at this time, as well as the diversification of eukaryotic algae, consistent with the previous hypothesis that the diversification of heterotrophic bacteria is linked to the emergence of large eukaryotic phytoplankton. The youngest clades correspond to the widespread phototrophic clades Prochlorococcus, Synechococcus, and Crocosphaera, whose diversification happened after the Phanerozoic Oxidation Event (0.45-0.4 Ga), in which oxygen concentrations had already reached their modern levels in the atmosphere and the ocean. Our work clarifies the timing at which abundant lineages of bacteria and archaea colonized the ocean, thereby providing key insights into the evolutionary history of lineages that comprise the majority of prokaryotic biomass in the modern ocean.

Oceanic Redox State During the Early Cambrian: Insights From Mo‐S Isotopes and Geochemistry of Himalayan Shales

AbstractThe Precambrian‐Cambrian (Pc‐C) boundary marks significant biological, atmospheric, and oceanic changes. These changes include extinction of the Ediacaran fauna, initiation of complex lifeforms, and oxygenation of the atmosphere and oceans. In this contribution, elemental and Mo‐S isotopic compositions of organic‐rich shales overlying the Pc‐C boundary from the Tal Formation, Lesser Himalaya, have been investigated. These datasets are used to reconstruct past oceanic redox state and sulfate concentrations. The principal component analysis of the elemental dataset identifies six major factors, with factors associated with organic matter and sulfide phases accounting for about half of the total variance. Iron speciation and Mo/U data suggest that the shales were deposited in anoxic and ferruginous deep water conditions. The δ98Mo data (1.5 ± 0.2‰) and their mass balance calculations indicate that the areal extent of sulfidic waters and pyrite burial rates were about 2–4 times higher during the Pc‐C transition than in the modern ocean. The pyrite‐δ34S values (3.6–8.3‰) for the Tal shales are isotopically heavier compared to modern‐day sedimentary pyrites (∼−21‰). Calculations involving earlier‐reported δ34S values for early Cambrian seawater and our measured pyrite‐δ34S data estimate the seawater sulfate concentration (8 ± 3 mM) during their deposition. This sulfate value for the Tal basin is higher than that reported for the late Neoproterozoic ocean (&lt;5 mM), attributable to increasing oxygen availability and continental supply during this time. The observed basinal conditions and high terrestrial input may have influenced metazoan diversification.

Globally limited but severe shallow-shelf euxinia during the end-Triassic extinction

One of the most severe extinctions of complex marine life in Earth’s history occurred at the end of the Triassic period (~201.4 million years ago). The marine extinction was initiated by large igneous province volcanism and has tentatively been linked to the spread of anoxic conditions. However, the global-scale pattern of anoxic conditions across the end-Triassic event is not well constrained. Here we use the sedimentary enrichment and isotopic composition of the redox-sensitive element molybdenum to reconstruct global–local marine redox conditions through the extinction interval. Peak δ98Mo values indicate that the global distribution of sulfidic marine conditions was similar to the modern ocean during the extinction interval. Meanwhile, Tethyan shelf sediments record pulsed, positive δ98Mo excursions indicative of locally oxygen-poor, sulfidic conditions. We suggest that pulses of severe marine de-oxygenation were restricted largely to marginal marine environments during the latest Triassic and played a substantial role in shallow-marine extinction phases at that time. Importantly, these results show that global marine biodiversity, and possibly ecosystem stability, were vulnerable to geographically localized anoxic conditions. Expanding present-day marine anoxia in response to anthropogenic marine nutrient supply and climate forcing may therefore have substantial consequences for global biodiversity and wider ecosystem stability.

Mixing time of heterogeneities in a buoyancy-dominated magma ocean

SUMMARY During the accretion stage, large impacts provided sufficient energy to melt the entire mantle into a terrestrial magma ocean. Processes occurring in the magma ocean may have led to the formation of heterogeneities still found in modern ocean island basalts. So far, no definitive mechanism exists to explain the survival of early heterogeneities for approximately 4.5 Ga. Addressing this question requires understanding the efficiency of convective mixing during both the early molten and the solid-state stages experienced by the Earth’s mantle. While mixing in the solid mantle and in an essentially crystallized magma ocean has been relatively well documented, the efficiency of convective mixing in a liquid magma ocean has received less attention. In this paper we characterized the mixing efficiency of a convecting fluid in a rotating spherical shell, accounting for inertial effects, by computing finite-time Lyapunov exponents (i.e. the Lagrangian strain rate). We conducted a series of numerical experiments for a regime where the influence of the buoyancy force dominates that of rotation and we derived scaling laws to predict the mixing efficiency. We found that for a terrestrial magma ocean, in its fully liquid state, mixing time is of the order of a few minutes or less, even for initially large (∼1000 km) heterogeneities. Therefore, passive early mantle heterogeneities cannot survive a fully molten magma ocean stage. This suggests that short-lived heterogeneities (e.g. 182Hf−182W) were either created at the end of the accretional stage, or were stored in deeper regions of the Earth.

Gephyrocapsa huxleyi (Emiliania huxleyi) as a model system for coccolithophore biology.

Coccolithophores are the most abundant calcifying organisms in modern oceans and are important primary producers in many marine ecosystems. Their ability to generate a cellular covering of calcium carbonate plates (coccoliths) plays a major role in marine biogeochemistry and the global carbon cycle. Coccolithophores also play an important role in sulfur cycling through the production of the climate-active gas dimethyl sulfide. The primary model organism for coccolithophore research is Emiliania huxleyi, now named Gephyrocapsa huxleyi. G. huxleyi has a cosmopolitan distribution, occupying coastal and oceanic environments across the globe, and is the most abundant coccolithophore in modern oceans. Research in G. huxleyi has identified many aspects of coccolithophore biology, from cell biology to ecological interactions. In this perspective, we summarize the key advances made using G. huxleyi and examine the emerging tools for research in this model organism. We discuss the key steps that need to be taken by the research community to advance G. huxleyi as a model organism and the suitability of other species as models for specific aspects of coccolithophore biology.

Mg isotopes of siliciclastic sediments on continental marginal sea: Insights for the potential to trace silicate weathering

In the last decade, much attention has been devoted to Mg isotopic behavior during various weathering processes. Nonetheless, whether Mg isotopes in terrigenous siliciclastic sediments in modern oceans can reflect continental weathering regimes remains unresolved. Understanding the major controls of Mg isotope fractionation in siliciclastic sediments is thus a prerequisite for decoding past Mg isotope records for tracing continental weathering history. In this study, we present mineralogical, elemental, and Mg isotopic compositions of terrigenous siliciclastic sediments in the Changjiang (Yangtze River) estuary and the adjacent continental shelf of the East China Sea. δ26Mg values of the clay-sized sediments vary from −0.15‰ to 0.00‰ and lack of the correlation with the proportion of different clay minerals. Our results suggest that the incipient to intermediate weathering processes are characterized by the progressive leaching of isotopically light Mg from silicates, leading to the enrichment of 26Mg in secondary clay minerals. Therefore, Mg isotopic variability of clay-sized sediments is primarily determined by catchment weathering, rather than by provenance lithology or mixing of clay minerals. An isotopic mass balance calculation indicates that the δ26Mg value of silicate weathering flux on a continental scale is ca. -0.60‰ to −0.40‰. The new constraint on the δ26Mg value of silicate weathering flux provides a new opportunity to better understand the Mg cycle. The Mg flux from silicate weathering in the Changjiang catchment is estimated as ∼15–17 × 1010 mol/yr, accounting for ca. 50% to 60% of the total Mg influx of Changjiang River into the ocean. In addition, numerical modeling with the up-to-date flux and isotope fractionation data have indicated that a slight enhancement of silicate weathering can potentially drive the rapid rise of Mg/Ca in seawater since late Cenozoic, but maintain the constancy of seawater δ26Mg as reported by literature. Our study demonstrates that Mg isotopes of clay-sized sediments can be used to constrain the relevant δ26Mg value of silicate weathering flux on a continental scale, which is a key parameter to trace the Mg cycle on Earth's surface.

Availability and type of energy regulate the global distribution of neritic carbonates

The study of carbonate rocks is primarily reliant on microfacies analysis, which is strongly based on the comparison with modern allochem assemblages. Despite the existence of several models aimed at comprehensively explaining, on the bases of abiotic factors, the distribution of carbonate-producing organisms, a global, quantitative and standardized overview of the composition of shallow-water carbonate sediments is still missing. Aiming to address this gap in knowledge, the current study provides a global database of the available quantitative data on neritic carbonate sediments. This is paired with satellite-based observations for the abiotic parameters. The results highlight a non-linear, multi-variable, dependence in the distribution of allochems and suggest that depth, temperature, and trophic state are, to a certain extent, interchangeable. The implication of which is a level of non-uniqueness for paleoenvironmental interpretation. The resulting distribution is rather continuous and stretches along an energy gradient. A gradient extending from solar energy, with autotrophs and symbiont-bearing organisms to chemical energy with heterotrophs. Further, quantitative data from modern oceans are still required to disentangle the remaining elements of uncertainty.

Heavy Mo isotope enrichment in the Pitcairn plume: Implications for the subduction cycle of anoxic sediments

Subduction redistributes elements between Earth's principal geochemical reservoirs, modifying the chemical composition of Earth's mantle, crust, atmosphere, and hydrosphere, and consequently having an impact on the evolution of life itself. Subduction of surface material that has been geochemically modified by low-temperature processes leads to mineralogical and chemical heterogeneities in mantle reservoirs over time and is recorded in modern ocean island basalts. One of the principal geochemical end members of the heterogeneous deep mantle, the enriched mantle 1 (EM-1) source of Pitcairn Island, has been attributed to the contribution of crustal material with vastly different chemical compositions and ages. The Mo isotope composition of lavas from Pitcairn Island constrains the nature of this recycled crustal component. Pitcairn lavas have elevated δ98/95Mo relative to the depleted mantle. The high δ98/95Mo is associated with high time-integrated 232Th/238U and 87Rb/86Sr, and low time-integrated 147Sm/144Nd and 238U/204Pb. These characteristics can be attributed to the recycling of nearly pristine pelagic sediments that were deposited in a Proterozoic anoxic deep-ocean into the sources of the Pitcairn Island lavas. The isotope composition of these lavas is similar to that of EM-1 hotspots from the South Atlantic, indicating the addition of reduced sediments in both of Earth's large low shear wave velocity provinces (LLSVPs). Consistent data from both locations imply that the subduction cycling of sedimentary redox-sensitive elements such as Mo, S, Se, and U into arc magmas was in these cases inefficient in the Precambrian and the chemical and isotopic signature of reduced sediments is preserved in the source of ocean island basalts bearing the EM-1 characteristics.

182W and 187Os constraints on the origin of siderophile isotopic heterogeneity in the mantle

Major and trace element abundances, including highly siderophile elements, and 187Os and 182W isotopic compositions were determined for ca. 89 Ma mafic and ultramafic rocks from the islands of Gorgona (Colombia) and Curaçao (Dutch Caribbean). The volcanic systems of both islands were likely associated with a mantle plume that generated the Caribbean Large Igneous Provence. The major and lithophile trace element characteristics of the rocks examined are consistent with the results of prior studies, and indicate derivation from both a chemically highly-depleted mantle component, and an enriched, or less highly-depleted mantle component. Highly siderophile element abundances for these rocks are generally similar to rocks with comparable MgO globally, indicating that the major source components were not substantially enriched or depleted in these elements. Rhenium-Os isotopic systematics of most rocks of both islands indicate derivation from a mantle source with an initial 187Os/188Os ratio between that of the contemporaneous average depleted mid-ocean ridge mantle and bulk silicate Earth. The composition may reflect either an average lower mantle signature, or global-scale Os isotopic heterogeneity in the upper mantle. Some of the basalts, as well as two of the komatiites, are characterized by calculated initial 187Os/188Os ratios 10–15 % higher than the chondritic reference. These more radiogenic Os isotopic compositions do not correlate with major or trace element systematics, and indicate a mantle source component that was most likely produced by either sulfide metasomatism or ancient Re/Os fractionation. Tungsten-182 isotopic compositions measured for rocks from both islands are characterized by variable μ182W values ranging from modern bulk silicate Earth-like to strongly negative values. The μ182W values do not correlate with major/trace element abundances or initial 187Os/188Os compositions. As with some modern ocean island basalt systems, however, the lowest μ182W value (−53) measured, for a Gorgona olivine gabbro, corresponds with the highest 3He/4He previously measured from the suite (15.8 R/RA). Given the lack of correlation with other chemical/isotopic compositions, the mantle component characterized by negative μ182W and possibly high 3He/4He is most parsimoniously explained to have formed as a result of isotopic equilibration between the mantle and core at the core-mantle boundary.

Bridging the extant and fossil record of planktonic foraminifera: implications for the Globigerina lineage

AbstractWe conducted a morphometric study and wall texture analysis on extant and fossil specimens of the planktonic foraminifera Globigerina falconensis plexus. Our global data reveal morphological inconsistencies between fossil and extant populations. Our results are significant as G. falconensis is widely used in palaeoceanographic studies in conjunction with its sister taxon G. bulloides. Morphologically these two species are similar, with the main difference being the distinctive apertural lip present in G. falconensis. We selected cores covering the entire stratigraphic range of G. falconensis, from the early Miocene to current day, spanning sites from high latitudes in the North Atlantic Ocean and the southern Indian Ocean to sites in equatorial regions. The morphology found in the modern ocean is not consistent with the Miocene holotype of Globigerina falconensis Blow described from lower Miocene sediments in Venezuela. A more lobate morphology evolved in the late Miocene, thus, a new name is required for this morphotype, coexisting in the modern oceans with G. falconensis s.s. We thus describe the new morphospecies, G. neofalconensis for the more lobate forms which evolved in the late Miocene and inhabit the modern oceans. Additionally, we report a pseudocancellate wall texture present in the G. falconensis plexus. We use the molecular sequences from the PR2 database to explore the generic attribution of the G. falconensis lineage, confirming its close relationship with G. bulloides and its retention in the genus Globigerina.