Continental Chemical Weathering Research Articles

Middle Ordovician climatic and oceanic destabilization in a slope-setting of the Yangtze platform, South China, and its role as a regional brake on the Ordovician radiations

During the Middle Ordovician, the Great Ordovician Biodiversification Event (GOBE) saw an accelerated diversification pulse in the marine metazoan richness, which has been linked to the oceanic and climatic changes. Here we have examined a deep-water slope succession, Xijinhe section, in Lower Yangtze region by integrating sedimentological and geochemical methods. This study highlights that the climatic and oceanic destabilization might have substantially impacted the marine biodiversity during the Middle Ordovician in South China. Three phases are identified based on lithological and geochemical variation patterns. During Phase I across the Early–Middle Ordovician transition (Floian–Dapingian), the TOC and abundances of redox sensitive elements (RSE) are relatively depleted, suggesting a suboxic-oxic environment in the slope area of Yangtze Sea. The continental chemical weathering intensity transit from stable to unstable in Phase I indicated by CIA (chemical index of alteration) that gradually fluctuate to lower values, potentially caused by the secular cooling. The slowly ameliorating climate and redox conditions advanced the biodiversification across the Early–Middle Ordovician transition. During the Phase II in the Darriwilian, the continental chemical weathering intensity continue to decrease and the concentrations of RSE start to rise. The values of Mn(%)*Co(ppm) become consistently lower than 0.4, and the bio-limited elements such as P, Ba, and Ni are substantially enriched correspondingly. This phenomenon implicates that a secular cooling climate would have resulted in oceanic destabilization by improving upwelling of deeper anoxic/euxinic and eutrophic water into epicontinental sea, potentially causing a deceleration in the biodiversification during the Darriwilian in South China. The Phase III across the Middle–Late Ordovician transition, witnesses the continuous decrease of CIA values and highest abundances of TOC and RSE though some minor fluctuations, indicating a possibly even more drastic oceanic destabilization relative to Phase II. Deeper anoxic/euxinic water continuously intruded and shoaled into the shelf area during the Phase III due to the enhanced upwelling. Consequently, the habitat of marine organisms in shallow water was contracted, and becoming harsher. Additionally, bio-limited elements such as P were released from anoxic sediments and recycle into the seawater during the Middle Ordovician, boosting primary productivity level and may further deplete oxygen in seawater. This unstable oceanic state during the Middle Ordovician, particularly Darriwilian, represented by high nutrients content in epi-continental sea and expanding anoxic/euxinic water, could be attributable for the deceleration of biodiversification in South China and potentially the spatially variable paces of biodiversification in different paleo-continents during the main phase of the GOBE.

Carbon‐cycle perturbations and intensified continental chemical weathering linked to volcanism during the Jenkyns Event in the Ordos Basin

The Jenkyns Event (~183 Ma) represents an exceptional warming period in the Jurassic, which is characterized by intense environmental and climate perturbation. The eruption of the Karoo‐Ferrar Large Igneous Province (K‐F LIP) triggered pronounced carbon isotope negative excursion (N‐CIE) in exogenic carbon reservoirs, global widespread organic carbon burial and extensive ocean anoxia. However, the synchronic coupling relationship between the carbon release, volcanic activity, and intense weathering induced by the K‐F LIP during this period remains poorly understood. In this study, detailed sedimentologic and geochemical studies were conducted on the terrestrial stratigraphy of the Lower Jurassic Fuxian Formation in the Ordos Basin. Three spore‐pollen assemblages have been identified, with the Cyathidites‐Deltoidospora‐Chasmatosporites assemblage suggesting a Pliensbachian age, the Classopollis‐Cycadopites‐Chasmatosporites assemblage indicating an early to middle Toarcian age, and the Cyathidites‐Cycadopites‐Psophosphaera assemblage indicating a late Toarcian age. The lower part of the Classopollis‐Cycadopites‐Chasmatosporites assemblage shows a negative CIE with a magnitude of 2.7‰, accompanied by organic carbon enrichment. Mercury concentrations and Hg/total organic carbon ratios also show peaks during the initial stage of the carbon isotope negative shift, implying a synchrony between volcanic activities and carbon perturbation. Furthermore, the Chemical Index of Alteration value has reached its maximum and the kaolinite content shows a sharp increase at the same position as the carbon isotope negative shift initiation, indicating a simultaneous enhancement of continental weathering during volcanic activity. The changing patterns of the continental weathering intensity encompassing the Jenkyns Event also indicate that continental weathering may have functioned as a significant approach to counteract the greenhouse effect caused by substantial volcanic CO2 emissions.

First report of Early Permian Tasmanite oil shales in northern Pangea with global implications

During the Late Paleozoic Ice Age (LPIA; particularly early Permian), organic material of the alga Tasmanites was extensively deposited in sediments of southern Gondwana, which formed the Tasmanite oil shales that have only been identified in Tasmania, Australia. It remains unclear whether other analogous geological records exist worldwide that formed at the same time, and the origin is enigmatic. This paper reports the first discovery of Tasmanite oil shales in northern Pangea, specifically in the Lucaogou Formation of the Junggar Basin, China, deposited during the Artinskian (ca. 290 Ma). The organic petrological features of Tasmanites are clearly visible, including thick-walled disks with tubes and radially arranged channels. These shales have markedly elevated C28/C29 steranes and tricyclic terpanes/hopanes ratios. Based on inorganic geochemical data, the salinity of the paleo-lake during deposition of the Tasmanite oil shale interval decreased abruptly from saline to brackish–freshwater. In addition, the pH changed from alkaline to nearly neutral, while the redox environment changed from anoxic to suboxic. Enhanced continental chemical weathering and the change in salinity of the paleo-lake occurred at the same time as global warming and large-scale glacier melting during the Artinskian, which promoted the habitat of the low-salinity tolerant Tasmanites. Our results provide new geological evidence for another occurrence of early Permian Tasmanite oil shales, indicating that Tasmanites flourishs and the associated oil shales may have been widely deposited at the end of the LPIA. The flourishment of Tasmanites archives biotic–environmental co-evolution.

Enhanced volcanic activity and long-term warmth in the middle Eocene revealed by mercury and osmium isotopes from IODP Expedition 369 Site U1514

Rapid plate reorganization may have influenced global climate during the Eocene; however, its linkage remains poorly constrained, particularly during the middle Eocene. To elucidate this tectonic–climatic relationship, here, we conducted a comprehensive analysis based on high-resolution mercury (Hg) and osmium (Os) abundance and isotope data obtained from the complete Eocene sedimentary sequence of Site U1514, drilled in the Mentelle Basin off southwest Australia. The Hg signals in this sedimentary sequence, which are characterized by significantly high enrichment and insignificant mass-independent fractionation (Δ199Hg) signal, confirm that the middle Eocene (∼45–38 Ma) was a period of persistent, increased volcanism, accompanied by intense tectonic activity. In particular, a remarkable seafloor volcanic eruption persisted for approximately 1.5 million years (∼42.0–40.5 Ma), immediately preceding the Middle Eocene Climate Optimum (MECO). Contemporaneously, the trends toward a slightly more radiogenic seawater 187Os/188Os (Osi) composition denote the prevalence of intensified continental weathering under a warm, humid climate during the middle Eocene, a phenomenon particularly evident during the MECO. Importantly, the Hg and Os records from Site U1514 reveal the occurrence of a multi-million-year warming reversal amid the long-term Eocene cooling trend, which likely contributed to significant CO2 reduction during the late Eocene. These findings significantly enhance our understanding of Eocene climate dynamics, which are fundamentally linked to intensive tectonic-driven volcanic activity and associated continental chemical weathering.

Four volcanically driven climatic perturbations led to enhanced continental weathering during the Late Triassic Carnian Pluvial Episode

The arid climate of the Late Triassic was interrupted by a particularly humid episode known as the Carnian Pluvial Episode (CPE; ca. 234–232 million years ago). The CPE is often linked to eruptions in the Wrangellia Large Igneous Province (LIP), and is assumed to have led to global warming, enhanced weathering, water deoxygenation, and biotic changes. However, direct evidence for a temporal link between volcanic activity and chemical weathering has not yet been established due to the lack of comprehensive records across the CPE. In this study, geochemical and mineralogical analyses are applied to a lacustrine stratigraphic succession of the Jiyuan Basin (North China) that captures the CPE in high resolution. We identify four distinct pulses of enhanced continental chemical weathering characterized by elevated Chemical Index of Alteration values and kaolinite contents. These peaks in continental weathering coincide with Hg/TOC enrichments and negative organic carbon isotope excursions that mark four short (∼400 kyr) but intense pulses of Wrangellia LIP volcanism. In combination with signs of increased humidity, our findings provide direct and independent evidence that Wrangellia LIP eruptions significantly altered CPE chemical weathering rates in response to global warming and wetting. The lake experienced eutrophication and water deoxygenation after each volcanic pulse but the swift recovery of carbon isotopes suggests that the system rapidly returned to conditions prior to the volcanic perturbation. Organic carbon burial facilitated by widespread dysoxic and anoxic waters, and CO2 consumption via enhanced weathering likely played crucial roles in the rapid climatic recovery after each volcanic pulse.

Dynamic redox and nutrient cycling response to climate forcing in the Mesoproterozoic ocean

Controls on Mesoproterozoic ocean redox heterogeneity, and links to nutrient cycling and oxygenation feedbacks, remain poorly resolved. Here, we report ocean redox and phosphorus cycling across two high-resolution sections from the ~1.4 Ga Xiamaling Formation, North China Craton. In the lower section, fluctuations in trade wind intensity regulated the spatial extent of a ferruginous oxygen minimum zone, promoting phosphorus drawdown and persistent oligotrophic conditions. In the upper section, high but variable continental chemical weathering rates led to periodic fluctuations between highly and weakly euxinic conditions, promoting phosphorus recycling and persistent eutrophication. Biogeochemical modeling demonstrates how changes in geographical location relative to global atmospheric circulation cells could have driven these temporal changes in regional ocean biogeochemistry. Our approach suggests that much of the ocean redox heterogeneity apparent in the Mesoproterozoic record can be explained by climate forcing at individual locations, rather than specific events or step-changes in global oceanic redox conditions.

Limited change in silicate chemical weathering intensity during the Permian–Triassic transition indicates ineffective climate regulation by weathering feedbacks

Vast emissions of volcanogenic greenhouse gases resulted in rapid global warming during the latest Permian mass extinction (LPME, ∼252 Ma), the impact of which on continental chemical weathering conditions was complex. Here, we compile Chemical Index of Alteration (CIA) records from 25 terrestrial and 12 marine sections with a near-global paleogeographic distribution to reconstruct the evolution of chemical weathering intensity of silicates during the LPME. This compilation shows that the CIA profiles, except those from the Australian Sydney and Bowen basins of the high-latitude Southern Hemisphere, exhibit either indiscernible changes or decreases through the LPME interval, contrary to previous inferences of increased silicate chemical weathering intensity. The lack of major changes in silicate chemical weathering intensity is further supported by the near uniformity of clay mineral assemblages through the LPME interval, with only minor increases of illite and chlorite and, if present, decreases in kaolinite content in some terrestrial sections. We infer a shift from dominantly transport-limited to kinetic-limited weathering regimes, likely caused by environmental climate factors such as widespread devegetation, river-flow changes (i.e., toward flashier and more intense discharge), and aridification during the earliest Triassic that effectively reduced water availability on land for water/rock reactions. Combined with limited changes in chemical weathering fluxes from previous estimates, our data imply possibly ineffective climate regulation by silicate chemical weathering at a (near-)global scale, despite high erosion rates, amid the intense global warming that followed the LPME.

Fluctuations of continental chemical weathering control primary productivity and redox conditions during the Earliest Cambrian

The Ediacaran – Cambrian transition witnessed dramatic changes in the marine environment that are thought to have strongly influenced biological evolution. Previous studies have linked biological innovations to palaeo‐redox changes and suggested that increased productivity is the primary driver of the marine environment. However, the primary productivity and redox control mechanism still need to be clarified. Here, we present new organic carbon isotopes, total organic carbon contents, major elements, and trace and rare earth elements in drill‐core ZK107 from South China to reveal the continental chemical weathering, primary productivity, and redox control mechanism during the Earliest Cambrian (E‐C). Our studies have shown intense continental weathering, and primary productivity fluctuations that were supported by weathering (CIA, Rb/Al) and productivity (Babio, P) indicators. Additionally, the quantitative reconstructed productivity proxies (PP18, PP21, PP23) indicate a high primary productivity level in the E‐C ocean, surpassing that of the modern oceans. The strengthening of continental weathering mainly causes high primary productivity because it can alter the nutrient supply to the oceans. We suggest that changes in primary productivity closely associated with continental weathering are the leading cause of marine anoxia during the E‐C. This study establish a linkage between the land and marine system during the E‐C, confirming the terrestrial controls on the marine chemical changes and providing new insights into understanding the evolution of the Earth's surface changes during the Ediacaran – Cambrian transition.

Anomalous weathering records in the Cleveland Basin (Yorkshire, UK) during the T‐OAE global warming

AbstractEarly Toarcian (~183 Ma) was marked by a global warming event which accelerated continental chemical weathering. To constrain the early Toarcian weathering intensity of a Cleveland Basin (Yorkshire, UK) region, this study employed its sediment chemical weathering proxies (potassium/aluminium (K/Al) and K/rubidium (K/Rb)). The K/Al and K/Rb exhibit an anomalous chemical weathering intensity signal from the contemporaneous warm, moist world. Variations in weathering intensity for the Yorkshire section inversely comply with detrital grain size changes (indicated by Al/silicon (Al/Si)). This finding implies that continental chemical weathering did not play a major role in changing detrital grain sizes in the Yorkshire sediments. Instead, short‐term sea‐level changes in the Cleveland Basin can explain the stratigraphic variations in detrital grain sizes. Anomalies of geochemical proxies for chemical weathering and eustatic sea‐level changes do exist at local scales possibly driven by Milankovitch cycle, which reminds us to be more careful when reconstructing palaeoclimate states.

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.

Spatiotemporal variation of Li isotopes in the Yarlung Tsangpo River basin (upper reaches of the Brahmaputra River): Source and process

The increase in marine Li isotope composition (δ7Li, ∼9‰) since the Cenozoic is possibly related to continental chemical weathering associated with tectonic uplift (e.g., the Tibetan Plateau [TP]). However, the reasons for the spatiotemporal variations of δ7Li in the rivers flowing through the TP are still under debate, hindering the understanding of the changes in seawater δ7Li. Herein, various geological samples, i.e. river waters, river suspended particulate materials, river sediments, hot springs and silicate rocks, from the Yarlung Tsangpo River basin, the largest river system in the TP, have been analyzed to understand the source and isotopic fractionation of dissolved Li in rivers flowing through high-altitude and tectonic regions. The Yarlung Tsangpo River has an unusually high dissolved Li concentration ([Li]dis) (0.5–313 μg/L, mean 58.4 μg/L, n=93) and low δ7Lidis values (+1.0‰–+14.7‰, mean +6.4‰, n=92) compared with most river waters. These results can be explained by the input of geothermal water with extremely high [Li]dis (5.5–34.4 mg/L, mean 15.7 mg/L, n=9) and low δ7Lidis (−1.7‰–+3.1‰, mean +1.0‰). Silicate weathering is probably responsible for elevated δ7Lidis in river water compared to geothermal water, but the binary mixture model results of silicate weathering and geothermal water do not support this speculation. Ongoing Li isotope fractionation between dissolved loads and secondary minerals has been suggested to be the main reason for the increased δ7Lidis in river water. Field study and adsorption experiment results support the view of continuous Li isotope fractionation in rivers. Physical erosion and chemical weathering processes that provide fresh secondary minerals to rivers as well as dissolved Li from geothermal water transported in rivers over long residence times promote Li isotope fractionation. Hence, with the emergence of a continental geothermal system, the tectonic activity may directly or indirectly induce the simultaneous increase in dissolved Li flux and δ7Lidis in rivers that eventually flow into the ocean. This can partially explain the increase in seawater δ7Li in the Late Cenozoic.

Spatiotemporal variations of chemical weathering intensity in large drainage basin and its potential climatic implications: A case study from the Yangtze River Valley

The knowledge on continental chemical weathering has a role in understanding carbon cycle and climate change. However, regional-scale spatiotemporal analysis of chemical weathering in large drainage basins is relatively seldom performed. In this study, based on 718 A- and C-horizon soil samples, we examined the spatiotemporal variations of chemical weathering intensity (i.e., the Chemical Index of Alteration (CIA)) in the Yangtze River Valley (YRV) by using trend surface analysis (TSA) and spatial correlation analysis (SCA). We found that: (1) the average CIA values of 68.4 and 68.5 for the A- and C-horizon soils reflect an overall intermediate chemical weathering in the YRV; (2) the weathering intensities follow a latitudinal distribution pattern that they increased from 50 to 70 in the north/northwest to 70–90 in the south/southeast of the YRV; (3) the general trend of chemical weathering is preferential leaching of Ca and Na over K; (4) TSA and SCA suggest a relatively dominant control of precipitation on the weathering intensity than temperature; (5) regions with frequent, long-duration and intense heavy precipitation (≥5 days/y and daily rainfall ≥50 mm) and heatwave (≥2 times/y, ≥15 days per time, and ≥ 40 °C) are featured with anomalous silicate weathering whose intensity was diminished from C- to A-horizon; and (6) the absolute differences of the mean CIA values between C- and A-horizon whether in the YRV or sub-regions were <1, indicating a stable silicate weathering. We conclude that significant latitude effect embodies the dominant control of monsoon climate on the chemical weathering in the YRV. Local climate extremes (e.g., rainstorms) are accompanied by anomalous silicate weathering. However, decreasing weathering intensity from bottom up does not necessarily indicate alleviated climate extremes, but probably the loss of terrestrial carbon stocks.

Sustained and intensified lacustrine methane cycling during Early Permian climate warming

Lakes are a major emitter of the atmospheric greenhouse gas methane (CH4); however, their roles in past climate warming episodes remain poorly understood owing to a scarcity of geological records. Here we report the occurrence of sustained and intensified microbial CH4 cycling in paleo-Lake Junggar in northwestern China, one of the largest known Phanerozoic lakes, during Early Permian climate warming. High-precision U-Pb geochronology refines the age of the upper Lucaogou Formation to the Artinskian, which marks a major glacial-to-postglacial climate transition. The 13C-enriched authigenic dolomites indicate active methanogenesis in the anoxic lake sediments, and 13C-depleted hopanes suggest vigorous methanotrophy in the water column. The intensification of CH4 cycling coincided with increasing global temperature, as evidenced from elevated continental chemical weathering. Our results suggest that the lacustrine CH4 emissions acted as a positive feedback to global warming and contributed to the demise of the Late Paleozoic Ice Age.

Geochemical characterization of major elements in Gurbantunggut Desert sediments, northwestern China and their regional variations

• Mineralogical maturity increased from the piedmont to the desert center. • Provenance controls the regional differences in major element compositions. • Transport, sorting, recycling, and chemical weathering affect the sand compositions. • River sands constitute a significant source of sands in this desert. • Extensive vegetation coverage contributes to the regional differences in this desert. Identifying the geochemical composition of desert sands in the Gurbantunggut Desert is essential for understanding the formation of desert dunes in the mid-latitudes. In this study, we collected samples of desert sands (125–250 μm), fluvial sands, and lacustrine sands across the Gurbantunggut Desert and calculated the sand drift potential at four meteorological stations. The sand samples from the Gurbantunggut Desert were mostly enriched in SiO 2 , while the other major elements were depleted compared to those of the Upper Continental Crust (UCC). The chemical weathering indices (α Al E, CIA, and WIP) indicate that the sand-sized sediments in the Gurbantunggut Desert are in the initial stage of continental chemical weathering. SiO 2 and K 2 O contents as well as mineralogical maturity of the desert sands increased from the piedmont to the desert center. UCC-normalized distribution patterns were also consistent along this transect due to the homogenization of desert sand composition, whereas the concentrations of other major elements (except for TiO 2 and MnO) decreased. We conclude that (1) regional variations in the composition of the Gurbantunggut Desert sands primarily reflect differences in provenance, transport, sorting, recycling of the sediments, and vegetation cover as well as the chemical weathering; and (2) differences in indices describing the major element composition of the sands reflect regional variations in provenance from the mountains to the depositional basin. Sands within piedmont rivers possess major element characteristics similar to those of dune sands in the region, suggesting that rivers represent a significant source of sands in the desert.

Lithium Isotope Geochemistry in the Barton Peninsula, King George Island, Antarctica

Lithium (Li) has two stable isotopes, 6Li and 7Li, whose large relative mass difference is responsible for significant isotopic fractionation during physico-chemical processes, allowing Li isotopes to be a good tracer of continental chemical weathering. Although physical erosion is dominant in the Polar regions due to glaciers, increasing global surface temperature may enhance chemical weathering, with possible consequences on carbon biogeochemical cycle and nutriment flux to the ocean. Here, we examined elemental and Li isotope geochemistry of meltwaters, suspended sediments, soils, and bedrocks in the Barton Peninsula, King George Island, Antarctica. Li concentrations range from 8.7 nM to 23.3 μM in waters, from 0.01 to 1.43 ppm in suspended sediments, from 9.56 to 36.9 ppm in soils, and from 0.42 to 28.3 ppm in bedrocks. δ7Li values are also variable, ranging from +16.4 to +41.1‰ in waters, from −0.4 to +13.4‰ in suspended sediments, from −2.5 to +6.9‰ in soils, and from −1.8 to +11.7‰ in bedrocks. Elemental and Li isotope geochemistry reveals that secondary phase formation during chemical weathering mainly control dissolved δ7Li values, rather than a mixing with sea salt inputs from atmosphere or ice melting. Likewise, δ7Li values of suspended sediments and soils lower than those of bedrocks indicate modern chemical weathering with mineral neoformation. This study suggests that increasing global surface temperature enhances modern chemical weathering in Antarctica, continuing to lower δ7Li values in meltwater with intense water-rock interactions.

Low source-inherited iron solubility limits fertilization potential of South American dust

Where atmospheric processing is weak due to low anthropogenic emissions, fertilization of iron-limited oceans by non-volcanic mineral dust aerosols strongly depends on iron solubility at the sources. Southern South America (SSA) is a pristine environment and the main dust supplier to the southern oceans, the most sensitive to iron fertilization. Thus, the present-day lack of SSA dust fertilization of the southern oceans is hypothesized to reflect low source-inherited iron bioavailability. However, a dearth of geochemical studies on SSA dust prevents testing this hypothesis. To remedy this, we conducted the first systematic sampling of SSA dust sources. Iron leaching experiments showed fractional solubilities of close-to-source dust (bulk) and dust-emitting surface sediments (<63 µm) in pure water (0.05 ± 0.05%), seawater (0.03 ± 0.04%) and 1% nitric acid (5 ± 6%) that imply a low mass-normalized fertilization potential of SSA dust compared to dust from other regions. Based on grain size, size-resolved mineralogy, elemental chemistry and iron speciation determinations, we found that variability in labile iron is enhanced by high clay contents, small grain size and higher proportions of paramagnetic versus non-paramagnetic iron, irrespective of oxidation state. The independence of the most labile, water-soluble iron on grain size and its strong negative correlation to the Chemical Index of Alteration may imply that we currently underestimate the role of coarse glaciogenic dust as a supplier of bioavailable iron during drier-than-present ice ages when continental chemical weathering was reduced, and during which enhanced supply of dust-borne bioavailable iron to the southern oceans is observed.

Enhanced continental chemical weathering during the multiple early Eocene hyperthermals: New constraints from the southern Indian Ocean

Multiple short-term (<105 years) global warming events (“hyperthermals”) occurred throughout the early Eocene. Chemical weathering of continental silicate rocks is considered to have played a key role in recovery from these transient global warming events via consumption of excess atmospheric CO2. However, although evidence of this negative feedback has been reported for the Paleocene–Eocene Thermal Maximum (PETM), the effectiveness of chemical weathering during other transient hyperthermals remains poorly constrained. Here, we newly report early Eocene marine Os isotope records including Eocene Thermal Maximum 2 (ETM2), the I1 event, and ETM3 at Ocean Drilling Program Site 752 in the southern Indian Ocean. We demonstrate that marine 187Os/188Os increased during the hyperthermal events that were less severe than the PETM. The intensity of continental silicate weathering increased by 18%–22%, 17%–21%, and 13%–16% during ETM2, the I1 event, and ETM3, respectively, compared to the background conditions. Based on a reconsidered formulation of an Os mass-balance model, the intensity of continental silicate weathering during the PETM was reassessed to be a 34%–42% increase relative to the pre-PETM level. Thus, the continental chemical weathering flux during the Eocene hyperthermals may have been up to half as large as that of the PETM. It is noteworthy that the ordering of the changes in continental silicate weathering did not agree with the ordering of the seawater temperature rise among these events. This weathering–warming inconsistency might be attributable to (1) potential underestimation of continental silicate weathering due to the emplacement of Large Igneous Provinces (LIPs) and related basalt weathering, such as the North Atlantic Igneous Province and Siletzia in western North America, (2) changes in the background level of weathering intensity, and/or (3) a secular decrease in continental weatherability through the long-lasting early Eocene warming trend.

Low marine sulfate levels during the initiation of the Cryogenian Marinoan glaciation

The microbial sulfate reduction plays a significant role in regulating marine organic matter degradation. Thus the variation of ancient marine sulfate levels is closely coupled with the changes in global organic carbon burials and Earth’s surface redox evolution in geological time. It is widely assumed that seawater sulfate concentration was deficient during the anoxic Cryogenian Marinoan glaciation (ca.650–635 Ma) which represents the most extreme icehouse condition in Earth’s history. However, such a low seawater sulfate level has not been explicitly confirmed. To address this, here we carried out pyrite content and sulfur isotope (δ34Spy) analysis of the Cryogenian non-glacial (the Datangpo Formation) and the Marinoan glacial successions (the Nantuo Formation) in South China. The Datangpo and Nantuo Formation show relatively high values of δ34Spy, ranging from +19.9 ‰ to +32.9 ‰, and low values of pyrite content (mean = 0.72 wt%). These pyrites are dominated by euhedral crystals with a rare occurrence of framboids, indicating an early diagenetic origin, i.e., pyrite formed in sediments with sulfate supplied from seawater. Using and a one-dimensional diffusion–advection-reaction (DAR) model, we calculate marine sulfate levels. The modeling results show that the seawater sulfate concentration is <1 mM during the transition from the top Datangpo to the basal Nantuo Formation, suggesting a shrink of the marine sulfate reservoir at the onset of Marinoan glaciation. We propose that the low marine sulfate concentration was resulted from a decrease in continental chemical weathering. This study provides a quantitative constraint on marine sulfate levels during the Cryogenian snowball Earth event, and it may shed new light on our understanding of the marine biogeochemical changes in the Neoproterozoic.

Intensified continental chemical weathering and carbon-cycle perturbations linked to volcanism during the Triassic\u2013Jurassic transition

Direct evidence of intense chemical weathering induced by volcanism is rare in sedimentary successions. Here, we undertake a multiproxy analysis (including organic carbon isotopes, mercury (Hg) concentrations and isotopes, chemical index of alteration (CIA), and clay minerals) of two well-dated Triassic–Jurassic (T–J) boundary sections representing high- and low/middle-paleolatitude sites. Both sections show increasing CIA in association with Hg peaks near the T–J boundary. We interpret these results as reflecting volcanism-induced intensification of continental chemical weathering, which is also supported by negative mass-independent fractionation (MIF) of odd Hg isotopes. The interval of enhanced chemical weathering persisted for ~2 million years, which is consistent with carbon-cycle model results of the time needed to drawdown excess atmospheric CO2 following a carbon release event. Lastly, these data also demonstrate that high-latitude continental settings are more sensitive than low/middle-latitude sites to shifts in weathering intensity during climatic warming events.

Global carbon sequestration through continental chemical weathering in a climatic change context

This study simulates carbon dioxide (CO2) sequestration in 300 major world river basins (about 70% of global surface area) through carbonates dissolution and silicate hydrolysis. For each river basin, the daily timescale impacts under the RCP 2.6 and RCP 8.5 climate scenarios were assessed relative to a historical baseline (1969–1999) using a cascade of models accounting for the hydrological evolution under climate change scenarios. Here we show that the global temporal evolution of the CO2 uptake presents a general increase in the annual amount of CO2 consumed from 0.247 ± 0.045 Pg C year−1 to 0.261 and 0.273 ± 0.054 Pg C year−1, respectively for RCP 2.6 and RCP 8.5. Despite showing a general increase in the global daily carbon sequestration, both climate scenarios show a decrease between June and August. Such projected changes have been mapped and evaluated against changes in hydrology, identifying hot spots and moments for the annual and seasonal periods.