Drawdown Of Atmospheric CO2 Research Articles

Climate forcing controls on carbon terrestrial fluxes during shale weathering

Climate influences near-surface biogeochemical processes and thereby determines the partitioning of carbon dioxide (CO2) in shale, and yet the controls on carbon (C) weathering fluxes remain poorly constrained. Using a dataset that characterizes biogeochemical responses to climate forcing in shale regolith, we implement a numerical model that describes the effects of water infiltration events, gas exchange, and temperature fluctuations on soil respiration and mineral weathering at a seasonal timescale. Our modeling approach allows us to quantitatively disentangle the controls of transient climate forcing and biogeochemical mechanisms on C partitioning. We find that ~3% of soil CO2 (1.02 mol C/m2/y) is exported to the subsurface during large infiltration events. Here, net atmospheric CO2 drawdown primarily occurs during spring snowmelt, governs the aqueous C exports (61%), and exceeds the CO2 flux generated by pyrite and petrogenic organic matter oxidation (~0.2 mol C/m2/y). We show that shale CO2 consumption results from the temporal coupling between soil microbial respiration and carbonate weathering. This coupling is driven by the impacts of hydrologic fluctuations on fresh organic matter availability and CO2 transport to the weathering front. Diffusion-limited transport of gases under transient hydrological conditions exerts an important control on CO2(g) egress patterns and thus must be considered when inferring soil CO2 drawdown from the gas phase composition. Our findings emphasize the importance of seasonal climate forcing in shaping the net contribution of shale weathering to terrestrial C fluxes and suggest that warmer conditions could reduce the potential for shale weathering to act as a CO2 sink.

Managing intermittency of renewable power in sustainable production of methanol, coupled with direct air capture

This study leverages worldwide wind data, process modelling, and life cycle assessment to reveal the potential of dynamic methanol production for atmospheric CO2 drawdown, while handling power intermittency and minimising reliance on reserve storage.

Air-sea carbon dioxide equilibrium: Will it be possible to use seaweeds for carbon removal offsets?

To limit global warming below 2°C by 2100, we must drastically reduce greenhouse gas emissions and additionally remove ~100-900 Gt CO2 from the atmosphere (carbon dioxide removal, CDR) to compensate for unavoidable emissions. Seaweeds (marine macroalgae) naturally grow in coastal regions worldwide where they are crucial for primary production and carbon cycling. They are being considered as a biological method for CDR and for use in carbon trading schemes as offsets. To use seaweeds in carbon trading schemes requires verification that seaweed photosynthesis that fixes CO2 into organic carbon results in CDR, along with the safe and secure storage of the carbon removed from the atmosphere for more than 100 years (sequestration). There is much ongoing research into the magnitude of seaweed carbon storage pools (e.g., as living biomass and as particulate and dissolved organic carbon in sediments and the deep ocean), but these pools do not equate to CDR unless the amount of CO2 removed from the atmosphere as a result of seaweed primary production can be quantified and verified. The draw-down of atmospheric CO2 into seawater is via air-sea CO2 equilibrium, which operates on time scales of weeks to years depending upon the ecosystem considered. Here, we explain why quantifying air-sea CO2 equilibrium and linking this process to seaweed carbon storage pools is the critical step needed to verify CDR by discrete seaweed beds and nearshore and open ocean aquaculture systems prior to their use in carbon trading.

Contrasting riverine K and Li isotope signatures during silicate weathering in the southeastern Tibetan Plateau

Mountain uplift produces steep slopes and rapid erosion rates, and hence exposes more silicate rocks to weathering and accelerates the drawdown of atmospheric CO2, driving global cooling over the Cenozoic. Riverine potassium (K) and lithium (Li) isotopes are two promising proxies for silicate weathering because the isotopes fractionate during secondary mineral formation associated with weathering and these two elements are highly enriched in silicate rocks. This study explores similarity and difference between K and Li isotope behaviors during weathering across the Lancang River in the southeastern Tibetan Plateau, in order to evaluate the role of these two isotopes in tracing silicate weathering in tectonically active mountains. Dissolved K and Li in the Lancang River mainstream are mainly derived from the dissolution of silicates. River waters are enriched in the heavy isotope of K (−0.35‰ to +0.05‰) and Li (+7.1‰ to +20.4‰) relative to suspended sediments (−0.56‰ to −0.42‰ and −2.3‰ to 0‰, respectively), and the element partitioning between dissolved and suspended loads controls dissolved δ7Li and δ41K values. Interesting, dissolved δ7Li and δ41K show the opposite evolution trends toward downstream. As the weathering intensity increases downstream (higher Si/(Na + K)⁎ ratios), the dissolved δ7Li values increase from 7.4‰ to 13.6‰, whereas dissolved δ41K values decrease from −0.04‰ to −0.26‰. Compared to its headwater with limited weathering, more secondary minerals (e.g., clays) are formed in the lower reaches (e.g., floodplains) with low physical erosion rates and high annual precipitation, driving more 6Li incorporated into clays, thus high dissolved δ7Li values downstream. While dissolved δ41K values and the fraction of 39K incorporated into secondary minerals are low in floodplains, this is consistent with observations that illite is a main K-bearing phase among clay minerals, and its content in the clay fraction in river sediment decreases as weathering intensity increases. Our study further supported that the increase in Cenozoic seawater δ7Li is related to weathering in floodplains rather than weathering of mountains, whereas K isotope fractionation mainly occurs in mountain regions. If Cenozoic seawater δ41K rise, as with δ7Li change, weathering at higher elevation may exerts more effect on high riverine and seawater δ41K values. This study improves our knowledge of K-Li isotope behaviors during present-day silicate weathering, and the response of K-Li isotopes in sedimentary archives to silicate weathering over geological time.

Chemical Alteration of Riverine Particles in Seawater and Marine Sediments: Effects on Seawater Composition and Atmospheric CO2

Numerous studies have shown that riverine particles react with seawater. Reactions include dissolution of reactive silicate minerals (e.g., feldspars) and formation of authigenic clays and carbonates. Previous studies have either focused on mineral dissolution (marine silicate weathering) or authigenic phase formation (reverse weathering). A comprehensive study that assesses all processes affecting the marine alteration of riverine particle has -to our knowledge- not yet been conducted. Our contribution aims to fill this gap. We first quantify cation exchange between seawater and riverine particles that occurs when particles enter the marine realm and show that significant global cation fluxes are induced by this process (-1.3 Tmol Na yr-1, -0.2 Tmol K yr-1, -0.4 Tmol Mg yr-1, +1.2 Tmol Ca yr-1) where the positive sign indicates cation release into seawater while the negative sign denotes uptake on particles. We then use thermodynamic and kinetic modeling to investigate how much of the suspended particle load dissolves in contact with seawater and estimate corresponding global release rates for dissolved cations and silica assuming congruent dissolution (+0.06 Tmol Na yr-1, +0.15 Tmol Ca yr-1, +2.8 Tmol Si yr-1). Subsequently, we investigate rates of mineral dissolution and authigenic clay and carbonate formation in marine sediments applying reactive transport modeling, porewater data and mass balance calculations. Our best estimates for net fluxes across the sediment/water interface (dissolution–mineral formation) result as +1.5 Tmol Na yr-1, -2.5 Tmol K yr-1, -2.0 Tmol Mg yr-1, +2.5 Tmol Ca yr-1, and +1.9 Tmol Si yr-1 where most of the Na and Ca release is induced by plagioclase dissolution, K is taken up in authigenic clays and Mg is removed from solution by authigenic clay and carbonate formation. We conclude that the alkalinity of seawater is not significantly affected by marine silicate alteration since cation release fluxes (Na, Ca) are as high as cation uptake fluxes (K, Mg) on equivalent basis. Moreover, marine silicate weathering and reverse weathering are closely coupled since Al required for clay formation is mostly provided by feldspar dissolution while Al removal in authigenic clay promotes and maintains feldspar dissolution in marine sediments. Authigenic carbonate formation in anoxic subsurface sediments sequesters significant amounts of carbon (2.5 Tmol C yr-1) according to our estimates where most of the Ca and alkalinity required for carbonate formation are provided by the dissolution of Ca-bearing silicate minerals. This hidden sedimentary cycle provides a sink for dissolved inorganic carbon that may drive a slow draw-down of atmospheric CO2 on geological timescales. Marine silicate alteration has an even stronger effect on the geochemical evolution of seawater by generating large fluxes of dissolved K, Mg, Ca and Si.

Mesoscale oceanographic meanders influence protist community function and structure in the southern Indian Ocean.

The interface between the nutrient-rich Southern Ocean and oligotrophic Indian Ocean creates unique environmental conditions that can strongly influence biological processes. We investigated protist communities across a mesoscale meander of the Subtropical Front within the Southern Indian Ocean. 18S V9 rDNA metabarcoding suggests a diverse protist community in which the dinoflagellates and parasitic Syndiniales were abundant. Diversity was highest in frontal waters of the mesoscale meander, with differences in community structure inside and outside the meander. While the overall community was dominated by mixotrophic taxa, the frontal boundary of the meander had increased abundances of heterotrophic taxa, with potential implications for net atmospheric CO2 drawdown. Pulse amplitude modulated (PAM) fluorimetry revealed significant differences in the photophysiology of phytoplankton communities inside and outside the meander. By using single-cell PAM microscopy, we identified physiological differences between dinoflagellate and coccolithophore taxa, which may have contributed to changes in photophysiology observed at community level. Overall, our results demonstrate that frontal areas have a strong impact on the composition of protist communities in the Southern Ocean with important implications for understanding biological processes in this region.

Soil carbon sequestration in global working lands as a gateway for negative emission technologies.

The ongoing climate crisis merits an urgent need to devise management approaches and new technologies to reduce atmospheric greenhouse gas concentrations (GHG) in the near term. However, each year that GHG concentrations continue to rise, pressure mounts to develop and deploy atmospheric CO2 removal pathways as a complement to, and not replacement for, emissions reductions. Soil carbon sequestration (SCS) practices in working lands provide a low-tech and cost-effective means for removing CO2 from the atmosphere while also delivering co-benefits to people and ecosystems. Our model estimates suggest that, assuming additive effects, the technical potential of combined SCS practices can provide 30%-70% of the carbon removal required by the Paris Climate Agreement if applied to 25%-50% of the available global land area, respectively. Atmospheric CO2 drawdown via SCS has the potential to last decades to centuries, although more research is needed to determine the long-term viability at scale and the durability of the carbon stored. Regardless of these research needs, we argue that SCS can at least serve as a bridging technology, reducing atmospheric CO2 in the short term while energy and transportation systems adapt to a low-C economy. Soil C sequestration in working lands holds promise as a climate change mitigation tool, but the current rate of implementation remains too slow to make significant progress toward global emissions goals by 2050. Outreach and education, methodology development for C offset registries, improved access to materials and supplies, and improved research networks are needed to accelerate the rate of SCS practice implementation. Herein, we present an argument for the immediate adoption of SCS practices in working lands and recommendations for improved implementation.

Ocean iron fertilization may amplify climate change pressures on marine animal biomass for limited climate benefit.

Climate change scenarios suggest that large-scale carbon dioxide removal (CDR) will be required to maintain global warming below 2°C, leading to renewed attention on ocean iron fertilization (OIF). Previous OIF modelling has found that while carbon export increases, nutrient transport to lower latitude ecosystems declines, resulting in a modest impact on atmospheric CO2 . However, the interaction of these CDR responses with ongoing climate change is unknown. Here, we combine global ocean biogeochemistry and ecosystem models to show that, while stimulating carbon sequestration, OIF may amplify climate-induced declines in tropical ocean productivity and ecosystem biomass under a high-emission scenario, with very limited potential atmospheric CO2 drawdown. The 'biogeochemical fingerprint' of climate change, that leads to depletion of upper ocean major nutrients due to upper ocean stratification, is reinforced by OIF due to greater major nutrient consumption. Our simulations show that reductions in upper trophic level animal biomass in tropical regions due to climate change would be exacerbated by OIF within ~20 years, especially in coastal exclusive economic zones (EEZs), with potential implications for fisheries that underpin the livelihoods and economies of coastal communities. Any fertilization-based CDR should therefore consider its interaction with ongoing climate-driven changes and the ensuing ecosystem impacts in national EEZs.

Mid-Pleistocene links between Asian dust, Tibetan glaciers, and Pacific iron fertilization

Increasing Asian dust fluxes, associated with late Cenozoic cooling and intensified glaciations, are conventionally thought to drive iron fertilization of phytoplankton productivity in the North Pacific, contributing to ocean carbon storage and drawdown of atmospheric CO2. During the early Pleistocene glaciations, however, productivity remained low despite higher Asian dust fluxes, only displaying glacial stage increases after the mid-Pleistocene climate transition (~800ka B.P.). We solve this paradox by analyzing an Asian dust sequence, spanning the last 3.6 My, from the Tarim Basin, identifying a major switch in the iron composition of the dust at ~800ka, associated with expansion of Tibetan glaciers and enhanced production of freshly ground rock minerals. This compositional shift in the Asian dust was recorded synchronously in the downwind, deep sea sediments of the central North Pacific. The switch from desert dust, containing stable, highly oxidized iron, to glacial dust, richer in reactive reduced iron, coincided with increased populations of silica-producing phytoplankton in the equatorial North Pacific and increased primary productivity in more northerly locations, such as the South China Sea. We calculate that potentially bioavailable Fe2+ flux to the North Pacific was more than doubled after the switch to glacially- sourced dust. These findings indicate a positive feedback between Tibetan glaciations, glaciogenic production of dust with enhanced iron bioavailability, and changes in North Pacific iron fertilization. Notably, this strengthened link between climate and eolian dust coincided with the mid-Pleistocene transition to increased storage of C in the glacial North Pacific and more intense northern hemisphere glaciations.

Implications of the Riverine Response to Enhanced Weathering for CO2 removal in the UK

Enhanced silicate weathering, the application of crushed calcium and magnesium-rich rocks to arable cropland, has been proposed as a potential negative emissions technology for the drawdown of atmospheric CO2. Previous estimates have suggested that enhanced silicate weathering (EW) has the potential to remove significant quantities of CO2, as much as 6–30 Mt CO2 yr−1 for the UK. However, if secondary carbonates are precipitated during the riverine transport of the products of EW, a portion of this CO2 will be re-released, lowering the net carbon dioxide removal (CDR) potential of the mitigation strategy. Here, we assess the fluvial response to EW in the UK by calculating the expected riverine carbonate precipitation due to the dissolution of 10–50 t ha−1 yr−1 of silicate rock on available arable cropland in major UK catchments.Increases in calcite saturation due to the export of soluble cations sourced from EW from soil to rivers are simulated to cross thresholds for spontaneous carbonate precipitation in several major UK river catchments (e.g. the Great Ouse, Thames). Catchments most susceptible to potential secondary carbonate precipitation are those with a high ratio of cropland to water discharge. On average, carbonate precipitation for major UK catchments is expected to make EW 16% (10 t ha−1), 21% (20 t ha−1) or 27% (50 t ha−1) less effective at removing CO2 than that predicted in the absence of such precipitation. Furthermore, when placing strict silica limitations on weathering reactions within soils, the CDR potential of EW is reduced considerably, to 0.23 Mt CO2 yr−1.Although reducing the CDR potential of EW, we suggest that under rapid weathering conditions, carbonate precipitation in UK rivers will prevent pH increases over the safe level for freshwater ecosystems (pH > 9). Together, the simulations suggest that ambient hydrological conditions may make certain UK agricultural areas less effective for CDR by EW and call for methods to quantify secondary carbonate precipitation in response to EW treatments and to further investigate the role of silica saturation in suppressing weathering reactions.

Late Cretaceous evolution of chemical weathering at the northeastern South American margin inferred from mineralogy and Hf-Nd isotopes

The origin of the global temperature decrease that initiated the last greenhouse-icehouse transition about 90 million years ago still remains debated. Among the potential processes driving long-term climate evolution over million-year timescales, this study investigates the possible impact of the uplift-weathering connection on the late Cretaceous atmospheric CO2 drawdown and associated cooling.We analysed a marine sediment record from the Demerara margin, using Nd and Hf isotopes in clay-size detrital fractions (ΔɛHf(t)clay) together with bulk and clay mineralogy and major element abundances to reconstruct the evolution of tectonic uplift and chemical weathering intensity in northeastern South America during the late Cretaceous. Our data indicate that silicate weathering intensified on the northeastern South American margin during the middle Campanian and the Maastrichtian, concomitant with an uplift phase of the Guiana craton. We propose that the tectonic pulse highlighted by apatite fission track data, argon/argon dating and primary silicate mineral evolution, was accompanied by an accelerated chemical weathering, which presumably acted as a sink for atmospheric CO2. By contrast, during the earlier late Turonian to early Campanian, period of relative tectonic quiescence, climate most likely acted as the main driver controlling the evolution of chemical weathering intensity. The main phase of enhanced weathering induced by the uplift of the northeastern South American margin occurred during the Campanian, thereby postdating the onset of global seawater temperature decrease (late Turonian). By inference, this regional event is unlikely to have triggered late Cretaceous cooling but it may have acted as an additional factor stabilizing colder climate conditions at that time.

Hafnium isotope evidence for enhanced weatherability at high southern latitudes during Oceanic Anoxic Event 2

The Oceanic Anoxic Event 2 (OAE 2; ca. ∼94 Ma) represents one of the most extreme carbon cycle perturbations of the Phanerozoic, which coincided with major environmental and climate reorganization in both terrestrial and marine realms. Chemical weathering of continental silicate rocks is thought to have played a crucial role during OAE 2, through enhanced release of bio-essential nutrients to the ocean, promoting high rates of marine primary production and organic carbon burial, but also due to its effect on atmospheric CO2 drawdown, which altogether possibly drove the OAE 2 termination. Yet, the evolution of continental chemical weathering during OAE 2 remains poorly defined, especially in high-latitude regions. In this study, we present a combined hafnium-neodymium isotope investigation of the clay-size detrital fraction (△εHfclay) of late Cenomanian to early Turonian sediments from the southwest Australian margin, at a site (International Ocean Discovery Program U1516) located in the southern high latitudes (∼62°S) during the late Cretaceous. The reliability of △εHfclay as a proxy for continental chemical weathering in ancient anoxic marine sediments was assessed by analyzing a suite of samples retrieved from methanogenic sediments experiencing marine silicate weathering at ocean margins, suggesting negligible effect of reverse weathering on hafnium-neodymium isotope compositions. At Site U1516, the early stage of OAE 2 was characterized by relatively low △εHfclay values (−5.9 ± 2), typical of reduced chemical weathering in nearby continental regions. At the onset of the most prominent carbon isotope excursion, an abrupt decrease in △εHfclay points towards accelerated export of poorly weathered sediments resulting from the abrupt reactivation of river systems in southwest Australia. This period was followed by a pronounced △εHfclay shift towards positive values, indicative of intensifying chemical weathering conditions during the OAE 2 interval showing the highest δ13C anomaly. Based on these results, we posit that enhanced hydrological cycle, most likely caused by a southward shift of the westerlies, led to a large increase in weatherability at southern high latitudes during peak OAE 2 warmth. This finding provides empirical support for the potential role played by high-latitude weathering systems in driving the termination of OAE 2, via weathering-driven consumption of atmospheric CO2 and accelerated riverine fluxes of nutrients leading to enhanced organic carbon burial in marine sediments.

Global reorganization of deep-sea circulation and carbon storage after the last ice age.

Using new and published marine fossil radiocarbon (14C/C) measurements, a tracer uniquely sensitive to circulation and air-sea gas exchange, we establish several benchmarks for Atlantic, Southern, and Pacific deep-sea circulation and ventilation since the last ice age. We find the most 14C-depleted water in glacial Pacific bottom depths, rather than the mid-depths as they are today, which is best explained by a slowdown in glacial deep-sea overturning in addition to a "flipped" glacial Pacific overturning configuration. These observations cannot be produced by changes in air-sea gas exchange alone, and they underscore the major role for changes in the overturning circulation for glacial deep-sea carbon storage in the vast Pacific abyss and the concomitant drawdown of atmospheric CO2.

Quantification of CO2 removal in a large-scale enhanced weathering field trial on an oil palm plantation in Sabah, Malaysia

Modeling studies show that large-scale deployment of enhanced rock weathering on croplands has the potential to reduce levels of atmospheric carbon dioxide by the end of the century. There is, however, a pressing need to verify model predictions through long-term field trials. Here we report results from the first 3 years of an ongoing enhanced weathering field trial, carried out on an oil palm plantation in Sabah, Malaysia. Crushed silicate rock was applied to three hydrologically isolated catchments, and three adjacent (paired) reference catchments were left untreated. The drawdown of atmospheric CO2 was quantified via the export of alkalinity in stream waters and changes in soil carbonate content. The amended and reference catchments were found to have a similar extent of CO2 drawdown via alkalinity export [respectively, 3.8 ± 0.8 (1 SD) and 3.7 ± 0.6 (1 SD) tCO2 ha−1] when all catchments were averaged over the study period (October 2018 to July 2021). However, differences were observed between the different catchment pairs (plots): two of the plots displayed a similar extent of CO2 removal for both the amended and reference catchments, but the third amended catchment had a higher extent of CO2 removal of ~1 tCO2 ha−1 relative to its adjacent reference catchment. The difference in CO2 removal rates determined for this plot can likely be attributed to increased weathering of silicate minerals in the amended catchment. Soil carbonate concentrations were on average <0.2 wt% CaCO3, but we report a small increase of ~0.03 wt% CaCO3 in the top 30 cm of soil in the amended soils relative to the reference catchments. The magnitude of CO2 drawdown via alkalinity export determined for these agricultural catchments is around an order of magnitude higher than in natural forested catchments in Sabah and similar to that of basaltic catchments. We show that these high weathering rates are primarily driven by weathering of carbonate fertilizers. The data presented from this field trial provide vital contextual information on the real-world efficacy and practicalities associated with the implementation of enhanced weathering for atmospheric CO2 removal that will help to inform further trials as well as wider-scale deployment.

Enhanced phosphorus recycling during past oceanic anoxia amplified by low rates of apatite authigenesis.

Enhanced recycling of phosphorus as ocean deoxygenation expanded under past greenhouse climates contributed to widespread organic carbon burial and drawdown of atmospheric CO2. Redox-dependent phosphorus recycling was more efficient in such ancient anoxic marine environments, compared to modern anoxic settings, for reasons that remain unclear. Here, we show that low rates of apatite authigenesis in organic-rich sediments can explain the amplified phosphorus recycling in ancient settings as reflected in highly elevated ratios of organic carbon to total phosphorus. We argue that the low rates may be partly the result of the reduced saturation state of sediment porewaters with respect to apatite linked to ocean warming and acidification and/or a decreased availability of calcium carbonate, which acts as a template for apatite formation. Future changes in temperature and ocean biogeochemistry, induced by elevated atmospheric CO2, may similarly increase phosphorus availability and accelerate ocean deoxygenation and organic carbon burial.

Plio‐Pleistocene Ocean Circulation Changes in the Gulf of Alaska and Its Impacts on the Carbon and Nitrogen Cycles and the Cordilleran Ice Sheet Development

AbstractThe modern Gulf of Alaska (GOA) is a Cordilleran Ice Sheet (CIS) region, estimated to be important for nutrient cycling and CO2 exchange. Little is known of the GOA evolution over the Pliocene and Pleistocene as well as its impact on the CIS development, when other evidence for changing North Pacific circulation has emerged. We analyzed Integrated Ocean Drilling Program Expedition 341 Site U1417 sediments, which extend through the Plio‐Pleistocene transition (4–1.7 Ma), focusing on productivity‐related biomarkers (alkenones, brassicasterol), siliceous microfossils and bulk carbon and nitrogen stable isotopes. Our results show two dominant water column regimes: one characterized by high silica and low organic matter (OM) preservation, containing microorganism remains from a mix of habitats (4–3.7 Ma) and a second characterized by low biogenic silica and increased OM preservation of microorganisms from dominantly open ocean habitats (3.33–3.32 Ma and 2.8–1.66 Ma). An increase of phytoplankton diversity (3.7–3.35 Ma, 3.19–2.82 Ma) characterizes the two transitions of water column conditions, from oxygenated to reductive, that we attribute to a change from ocean mixing to strong stratified conditions with some occasional mixing. The biogeochemical changes in the GOA follow 400 and 100 kyr eccentricity cycles which are also reflected in changes in the CIS. We conclude that the CIS expansion created high nutrient low chlorophyll conditions in the GOA during the Mid Piacenzian Warm Period and the early Pleistocene. In turn, positive feedbacks increased marine productivity export, atmospheric CO2 drawdown and further CIS expansion.

The supercontinent cycle and Earth's long-term climate.

Earth's long-term climate has been profoundly influenced by the episodic assembly and breakup of supercontinents at intervals of ca. 500 m.y. This reflects the cycle's impact on global sea level and atmospheric CO2 (and other greenhouse gases), the levels of which have fluctuated in response to variations in input from volcanism and removal (as carbonate) by the chemical weathering of silicate minerals. Supercontinent amalgamation tends to coincide with climatic cooling due to drawdown of atmospheric CO2 through enhanced weathering of the orogens of supercontinent assembly and a thermally uplifted supercontinent. Conversely, breakup tends to coincide with increased atmospheric CO2 and global warming as the dispersing continental fragments cool and subside, and weathering decreases as sea level rises. Supercontinents may also influence global climate through their causal connection to mantle plumes and large igneous provinces (LIPs) linked to their breakup. LIPs may amplify the warming trend of breakup by releasing greenhouse gases or may cause cooling and glaciation through sulfate aerosol release and drawdown of CO2 through the chemical weathering of LIP basalts. Hence, Earth's long-term climatic trends likely reflect the cycle's influence on sea level, as evidenced by Pangea, whereas its influence on LIP volcanism may have orchestrated between Earth's various climatic states.

Chemical weathering signatures at Mt. Achernar, Central Transantarctic Mountains II: Surface exposed sediments

Mt Achernar Moraine is a high altitude, high latitude blue ice moraine where typical conditions preclude the presence of liquid water. Cosmogenic and salt accumulation dating indicate that the moraine’s surface is progressively older away from the active ice margin, with surface exposure ages up to 1 Ma. We analyze the chemical and mineralogical transformations in the <63 µm fraction along transects across the moraine. Data include bulk chemical composition, crystalline mineralogy by X-ray diffraction (XRD), and the composition of amorphous or low abundance products of chemical weathering by sequential extraction. These data are analyzed by multiple regression as a function of exposure age and as a function of composition of the moraine’s cobble and pebble-sized clasts. Change with exposure age is defined by the development of salts and carbonate minerals along with the input of detrital material, principally from sedimentary rocks. Clay minerals and amorphous cements breakdown as detrital material in proportions far above their abundance in the rock clasts, whereas framework silicates (i.e. feldspars and quartz) break down in relatively small proportions. Both the carbonate minerals and some of the salts form from atmospheric acids (i.e. H2CO3) that in turn react with other minerals. Mass balance shows that the input of these atmospheric acids balances with gains in authigenic smectites, zeolites, and amorphous material. Many of these minerals also form in the subglacial environment, but are poorly represented in the underlying rock, suggesting a similar chemical weathering regime in both the subglacial and surface environments of this hyper cold and arid setting. The rate of CO2 drawdown into carbonate minerals increases as the moraine progressively thickens, from 3 mg·m2·a−1 in freshly emerging sediments to ∼50 mg·m2·a−1 after 500 ka of exposure. Weathering from acidic aerosols is proportional to atmospheric flux documented in ice cores and does not vary with moraine thickness. The carbonate mineral formation rates are more than an order of magnitude below those of the subglacial environment and as much as two orders of magnitude below those found in warm desert soils. Nevertheless, the drawdown of atmospheric CO2 into carbonate minerals occurs in a terrestrial setting where water exists only in vapor form.

Relationship between glacial CO2 drawdown and mercury cycling in the western South Atlantic: An isotopic insight

Abstract Pronounced changes in the deep Atlantic circulation occurred during glacial stages, which affected the global carbon distribution and the biogeochemical cycles of other elements. Previous studies demonstrated that oceanic mercury is sensitive to the same kind of processes that affect the carbon cycle in glacial–interglacial time scales. We used Hg isotopes to elucidate Hg cycling during the last two glacial–interglacial transitions in the subtropical western South Atlantic. Mass-dependent fractionation (MDF, δ202Hg) and mass-independent fractionation (MIF, Δ199Hg) show significant variations and shift toward higher and lower values during the penultimate and Last Glacial Maximum periods, respectively. δ202Hg variability is in-phase with periods of lower atmospheric CO2 and benthic δ13C, suggesting that MDF is affected by the same mechanisms that led to atmospheric CO2 drawdown during glacial stages. In contrast, terrestrial Hg input to our site, boosted by lower sea level and exposure of the continental shelf, dominates the Δ199Hg variability.

Oligocene moisture variations as evidenced by an aeolian dust sequence in Inner Mongolia, China

The aridification of Central Asia since the Eocene has widespread evidence, but climate-controlled environmental reorganizations during the Oligocene remain ambiguous. We employed environmental magnetic, mineralogical and geochemical methods on a latest Eocene to late Oligocene terrestrial sequence in Inner Mongolia, China, to examine how global climatic trends and regional factors influenced the evolution of moisture and weathering in the region. Highlighting the climatic influence, our weathering and rainfall proxy data document the drawdown of atmospheric CO2 and global cooling during the early Oligocene semi-arid phase, which culminated in the Early Oligocene Aridification Event at 31 Ma. Moreover, for the first time in the terrestrial eastern Central Asian setting, we provide geochemical and geophysical evidence for a second major Oligocene aridification event nearly synchronous to the mid-Oligocene Glacial Maximum at around 28 Ma. These aridification events were interrupted by periods of increased rainfall and weathering and can be associated with the terminations of glacial events seen in marine oxygen isotope records.