Atmospheric CO2 Consumption by Chemical Weathering in the Main Tributaries of the Yellow River: Tao He, Huang Shui, and Datong He, Originating From the Northeastern Qinghai-Tibet Plateau

The Tao He, Huang Shui, and Datong He originate from the northeastern margin of the Qinghai-Tibet Plateau (QTP) and flow into the Yellow River on the Loess Plateau (LP), all with a basin area exceeding 15,000 km2, and are the three largest tributaries of the Yellow River QTP sub-basin. Water samples were collected at the river outlets, the QTP section, the transition zone between the QTP and the LP, and the LP section of each river. These water samples were used to explore CO2 consumption by chemical weathering and its control mechanisms. Runoff and physical erosion are the main factors controlling chemical weathering in the three rivers. The increase of relief ratio in the transition zone between the QTP and the LP makes the chemical weathering particularly intense in this area. The total CO2 consumption rates by chemical weathering in the Tao He and Huang Shui transition zones are 1.4 times and 1.7 times greater than in their QTP sections, and 1.7 times and 2.3 times greater than in their LP sections, respectively. In contrast, due to the high relief ratio of 8‰ in the Datong He transition zone, the residence time of the water is extremely short, and unweathered fine-grained materials are delivered downstream to continue weathering. The influence of differential lithology distribution on chemical weathering includes that the Datong He QTP section with carbonate exposure presents the most intense carbonate weathering in that basin, and the Tao He transition zone has low silicate weathering resulting from the distribution of early Permian strata. In addition, groundwater recharge most likely influenced the silicate weathering of Huang Shui significantly. The total area of the three rivers accounts for 25% of the Yellow River QTP sub-basin, while their contribution to the total CO2 consumption flux by chemical weathering approximates 36%. The silicate weathering of the northern QTP rivers is lower than the global average and significantly lower than those of the southern QTP rivers. However, carbonate weathering of the QTP rivers exhibit no north-south regional differences.

The effect of lithology on the relationship between denudation rate and chemical weathering pathways

The denudation of rocks in mountain belts exposes a range of fresh minerals to the surface of the Earth that are chemically weathered by acidic and oxygenated fluids. The impact of the resulting coupling between denudation and weathering rates fundamentally depends on the types of minerals that are weathering. Whereas silicate weathering sequesters CO2, the combination of sulfide oxidation and carbonate dissolution emits CO2 to the atmosphere. Here, we combine the concentrations of dissolved major elements in stream waters with 10Be basin-wide denudation rates from 35 small catchments in eastern Tibet to elucidate the importance of lithology in modulating the relationships between denudation rate, chemical weathering pathways, and CO2 consumption or release. Our catchments span three orders of magnitude in denudation rate in low-grade flysch, high grade metapelites, and granitoid rocks. For each stream, we estimate the concentrations of solutes sourced from silicate weathering, carbonate dissolution, and sulfide oxidation using a mixing model. We find that for all lithologies, cation concentrations from silicate weathering are largely independent of denudation rate, but solute concentrations from carbonates and, where present, sulfides increase with increasing denudation rate. With increasing denudation rates, weathering may, therefore, shift from consuming to releasing CO2 in both (meta)sedimentary and granitoid lithologies. We find that catchments draining high grade metamorphic rocks have systematically higher concentrations of sulfate from sulfide weathering than catchments containing weakly metamorphosed sediments. Moreover, our data provide tentative evidence that sulfate concentrations in these catchments are potentially more sensitive to denudation rate. We propose that changes in the sulfur oxidation state during prograde metamorphism of pelites in the mid-crust could lead to sulfate reduction that is even more complete than in low-grade sediments and provides a larger sulfide source for oxidation upon re-exposure of the rocks. In this case, the elevated concentration of sulfate in catchments draining high-grade metapelites would suggest that exposure of an increasing fraction of metamorphic rocks during orogenesis could lead to a boost in the release of CO2 that is independent of denudation rate.

A Strontium and Hydro-Geochemical Perspective on Human Impacted Tributary of the Mekong River Basin: Sources Identification, Fluxes, and CO2 Consumption

As the largest and most representative tributary of the Mekong River, the Mun River Basin (MRB) provides critical understanding of regional hydro-geochemical features and rock weathering processes on a basin scale. The present study measured strontium (Sr) isotopes with hydro-geochemistry data of 56 water samples in detail in the MRB in northeast Thailand. The dissolved Sr contents and 87Sr/86Sr isotopic ratios were reported to be 8.7–344.6 μg/L (average 126.9 μg/L) and 0.7085–0.7281 (average 0.7156), respectively. The concentrations of dissolved Sr in the mainstream slightly decreased from upstream to downstream, while the variation trend of 87Sr/86Sr was on the contrary. Correlation analysis showed that Na+ strongly correlated with Cl− (0.995, p < 0.01), while Ca2+ exhibited weak relationships with SO42− (0.356, p < 0.01). Samples of the MRB exhibited lower Mg2+/Na+, Ca2+/Na+, HCO3−/Na+ and 1000Sr/Na ratios, and gathered around the end-member of evaporite dissolution, with slight shift to silicate weathering end-member, demonstrating the dominant contribution of evaporite dissolution and silicate weathering on dissolved loads. Comparing with data of major world rivers from previous research, our results remained consistency with rivers draining through similar geological conditions. The dissolved Sr flux to the adjacent Mekong River was estimated to be 20.7 tons/year. In accordance with the forward model, silicate weathering rate and CO2 consumption rate during dry season were calculated to be 0.73 tons/km2/year and 1.94 × 104 mol/km2/year, and may get underestimated due to intense water consumption by extensive agricultural activities. The superimposed effect of anthropogenic impacts on the water environment could enhance chemical weathering, and thus should be taken into account in regional ion cycles and carbon budgets. These findings highlight the coupling analysis of Sr isotopes and hydro-geochemistry in Earth surface processes and provide basic investigation for sustainable regional water treatment mechanisms in the pan basin of the Mekong River.

Neogene continental denudation and the beryllium conundrum

Reconstructing Cenozoic history of continental silicate weathering is crucial for understanding Earth’s carbon cycle and greenhouse history. The question of whether continental silicate weathering increased during the late Cenozoic, setting the stage for glacial cycles, has remained controversial for decades. Whereas numerous independent proxies of weathering in ocean sediments (e.g., Li, Sr, and Os isotopes) have been interpreted to indicate that the continental silicate weathering rate increased in the late Cenozoic, beryllium isotopes in seawater have stood out as an important exception. Beryllium isotopes have been interpreted to indicate stable continental weathering and/or denudation rates over the last 12 Myr. Here we present a Be cycle model whose results show that variations in the 9Be weathering flux are counterbalanced by near-coastal scavenging while the cosmogenic 10Be flux from the upper atmosphere stays constant. As a result, predicted seawater 10Be/9Be ratios remain nearly constant even when global denudation and Be weathering rates increase by three orders of magnitude. Moreover, 10Be/9Be records allow for up to an 11-fold increase in Be weathering and denudation rates over the late Cenozoic, consistent with estimates from other proxies. The large increase in continental weathering indicated by multiple proxies further suggests that the increased CO2 consumption by continental weathering, driven by mountain-building events, was counterbalanced by other geological processes to prevent a runaway icehouse condition during the late Cenozoic. These processes could include enhanced carbonate dissolution via pyrite weathering, accelerated oxidation of fossil organic carbon, and/or reduced basalt weathering as the climate cooled.

Rapid and sustained environmental responses to global warming: the Paleocene–Eocene Thermal Maximum in the eastern North Sea

The Paleocene–Eocene Thermal Maximum (PETM; ∼ 55.9 Ma) was a period of rapid and sustained global warming associated with significant carbon emissions. It coincided with the North Atlantic opening and emplacement of the North Atlantic Igneous Province (NAIP), suggesting a possible causal relationship. Only a very limited number of PETM studies exist from the North Sea, despite its ideal position for tracking the impact of both changing climate and NAIP activity. Here we present sedimentological, mineralogical, and geochemical proxy data from Denmark in the eastern North Sea, exploring the environmental response to the PETM. An increase in the chemical index of alteration and a kaolinite content up to 50 % of the clay fraction indicate an influx of terrestrial input shortly after the PETM onset and during the recovery, likely due to an intensified hydrological cycle. The volcanically derived zeolite and smectite minerals comprise up to 36 % and 90 % of the bulk and clay mineralogy respectively, highlighting the NAIP's importance as a sediment source for the North Sea and in increasing the rate of silicate weathering during the PETM. X-Ray fluorescence element core scans also reveal possible hitherto unknown NAIP ash deposition both prior to and during the PETM. Geochemical proxies show that an anoxic to sulfidic environment persisted during the PETM, particularly in the upper half of the PETM body with high concentrations of molybdenum (MoEF > 30), uranium (UEF up to 5), sulfur (∼ 4 wt %), and pyrite (∼ 7 % of bulk). At the same time, export productivity and organic-matter burial reached its maximum intensity. These new records reveal that negative feedback mechanisms including silicate weathering and organic carbon sequestration rapidly began to counteract the carbon cycle perturbations and temperature increase and remained active throughout the PETM. This study highlights the importance of shelf sections in tracking the environmental response to the PETM climatic changes and as carbon sinks driving the PETM recovery.