ALBERT

Description: Basalt weathering is one of many relevant processes balancing the global carbon cycle via land-ocean alkalinity fluxes. The CO2 consumption by weathering can be calculated using alkalinity and is often scaled with runoff and/or temperature. Here it is tested if information on the surface age distribution of a volcanic system is a useful proxy for changes in alkalinity production with time. A linear relationship between temperature normalized alkalinity fluxes and the Holocene area fraction of a volcanic field was identified, using information from 33 basalt volcanic fields, with an r2=0.91. This relationship is interpreted as an aging function and suggests that fluxes from Holocene areas are ~10 times higher than those from old inactive volcanic fields. However, the cause for the decrease with time is probably a combination of effects, including a decrease in alkalinity production from surface near material in the critical zone as well as a decline in hydrothermal activity and magmatic CO2 contribution. A comparison with global models suggests, that global alkalinity fluxes considering Holocene active basalt areas are ~70% higher than the average from these models imply. The contribution of Holocene areas to the global basalt alkalinity fluxes is however only ~6%, because identified, mapped Holocene basalt areas cover only ~1% of the existing basalt areas. The large trap basalt proportion on the global basalt areas today reduces the relevance of the aging effect. However, the aging effect might be a relevant process during periods of globally, intensive volcanic activity, which remains to be tested.

Description: Basalt weathering is one of many relevant processes balancing the global carbon cycle via land–ocean alkalinity fluxes. The CO2 consumption by weathering can be calculated using alkalinity and is often scaled with runoff and/or temperature. Here, it is tested if the surface age distribution of a volcanic system derived by geological maps is a useful proxy for changes in alkalinity production with time. A linear relationship between temperature normalized alkalinity fluxes and the Holocene area fraction of a volcanic field was identified using information from 33 basalt volcanic fields, with an r2=0.93. This relationship is interpreted as an aging function and suggests that fluxes from Holocene areas are ∼10 times higher than those from old inactive volcanic fields. However, the cause for the decrease with time is probably a combination of effects, including a decrease in alkalinity production from material in the shallow critical zone as well as a decline in hydrothermal activity and magmatic CO2 contribution. The addition of fresh reactive material on top of the critical zone has an effect in young active volcanic settings which should be accounted for, too. A comparison with global models suggests that global alkalinity fluxes considering Holocene basalt areas are ∼60 % higher than the average from these models imply. The contribution of Holocene areas to the global basalt alkalinity fluxes is today however only ∼5 %, because identified, mapped Holocene basalt areas cover only ∼1 % of the existing basalt areas. The large trap basalt proportion on the global basalt areas today reduces the relevance of the aging effect. However, the aging effect might be a relevant process during periods of globally intensive volcanic activity, which remains to be tested.

Description: Basalt weathering is one of many relevant processes balancing the global carbon cycle via land-ocean alkalinity fluxes. The CO2 consumption by weathering can be calculated using alkalinity and is often scaled with runoff and/or temperature. Here it is tested if information on the surface age distribution of a volcanic system is a useful proxy for changes in alkalinity production with time. A linear relationship between temperature normalized alkalinity fluxes and the Holocene area fraction of a volcanic field was identified, using information from 33 basalt volcanic fields, with an r2=0.91. This relationship is interpreted as an aging function and suggests that fluxes from Holocene areas are ~10 times higher than those from old inactive volcanic fields. However, the cause for the decrease with time is probably a combination of effects, including a decrease in alkalinity production from surface near material in the critical zone as well as a decline in hydrothermal activity and magmatic CO2 contribution. A comparison with global models suggests, that global alkalinity fluxes considering Holocene active basalt areas are ~70% higher than the average from these models imply. The contribution of Holocene areas to the global basalt alkalinity fluxes is however only ~6%, because identified, mapped Holocene basalt areas cover only ~1% of the existing basalt areas. The large trap basalt proportion on the global basalt areas today reduces the relevance of the aging effect. However, the aging effect might be a relevant process during periods of globally, intensive volcanic activity, which remains to be tested.

Description: Carbonate rocks are a peculiarity of the Earth relative to other planets in the solar system. Large terrestrial areas are covered by carbonate lithology, which actively reacts with atmospheric/biospheric CO2. Although carbonate rocks represent a major component of the global carbon cycle, their intensity and rates of chemical weathering have been overlooked. In this study, we examine three global databases of rivers and springs draining carbonate regions under various climate conditions (from −15 °C to +30 °C). Using Ca2+ + Mg2+ concentrations as a proxy, we show that carbonate weathering intensity depends upon land temperature according to a boomerang-type relationship, with maximum dissolution between 10 and 15 °C. We show that this pattern is primarily controlled by thermodynamics if we assume that the partial pressure of CO2 in soil (pCO2) increases from atmospheric-like levels under cold climate up to 100 times the present day atmospheric concentration under hot climate. The link between soil pCO2 and land temperature is still not very well known, but by using three different published predictive soil pCO2 vs. T curves, we show that the boomerang shape can be, at least qualitatively, reproduced. This study shows that more data on carbonate weathering in various environments are needed to predict with more accuracy the role that carbonate lithologies and overlying ecosystems could play in the Anthropocene.

Description: Basalt weathering is one of many relevant processes balancing the global carbon cycle via land–ocean alkalinity fluxes. The CO2 consumption by weathering can be calculated using alkalinity and is often scaled with runoff and/or temperature. Here, it is tested if the surface age distribution of a volcanic system derived by geological maps is a useful proxy for changes in alkalinity production with time. A linear relationship between temperature normalized alkalinity fluxes and the Holocene area fraction of a volcanic field was identified using information from 33 basalt volcanic fields, with an r2=0.93. This relationship is interpreted as an aging function and suggests that fluxes from Holocene areas are ∼10 times higher than those from old inactive volcanic fields. However, the cause for the decrease with time is probably a combination of effects, including a decrease in alkalinity production from material in the shallow critical zone as well as a decline in hydrothermal activity and magmatic CO2 contribution. The addition of fresh reactive material on top of the critical zone has an effect in young active volcanic settings which should be accounted for, too. A comparison with global models suggests that global alkalinity fluxes considering Holocene basalt areas are ∼60 % higher than the average from these models imply. The contribution of Holocene areas to the global basalt alkalinity fluxes is today however only ∼5 %, because identified, mapped Holocene basalt areas cover only ∼1 % of the existing basalt areas. The large trap basalt proportion on the global basalt areas today reduces the relevance of the aging effect. However, the aging effect might be a relevant process during periods of globally intensive volcanic activity, which remains to be tested.

Description: Loess sediments are windblown silt deposits with, in general, a carbonate grain content of up to 30%. While regionally, loess was reported to increase weathering fluxes substantially, the influence on global weathering fluxes remains unknown. Especially on glacial‐interglacial time scales, loess weathering fluxes might have contributed to land‐ocean alkalinity flux variability since the loess areal extent during glacial epochs was larger. To quantify loess weathering fluxes, global maps representing the loess distribution were compiled. Water chemistry of rivers draining recent loess deposits suggests that loess contributes over‐proportionally to alkalinity concentrations if compared to the mean of alkalinity concentrations of global rivers (~4,110 µeq L−1 for rivers draining loess deposits and ~1,850 µeq L−1 for the total of global rivers), showing comparable alkalinity concentration patterns in rivers as found for carbonate sedimentary rocks. Loess deposits, covering ~4% of the ice‐ and water‐free land area, increase calculated global alkalinity fluxes to the coastal zone by 16%. The new calculations lead to estimating a 4% higher global alkalinity flux during the Last Glacial Maximum (LGM) compared to present fluxes. The effect of loess on that comparison is high. Alkalinity fluxes from silicate‐dominated lithological classes were ~28% and ~30% lower during the LGM than recent (with loess and without loess, respectively), and elevated alkalinity fluxes from loess deposits compensated for this. Enhanced loess weathering dampens due to a legacy effect changes in silicate‐dominated lithologies over the glacial‐interglacial time scale.

Description: The carbon cycle component of the newly developed Earth System Model of intermediate complexity CLIMBER-X is presented. The model represents the cycling of carbon through atmosphere, vegetation, soils, seawater and marine sediments. Exchanges of carbon with geological reservoirs occur through sediment burial, rock weathering and volcanic degassing. The state-of-the-art HAMOCC6 model is employed to simulate ocean biogeochemistry and marine sediments processes. The land model PALADYN simulates the processes related to vegetation and soil carbon dynamics, including permafrost and peatlands. The dust cycle in the model allows for an interactive determination of the input of the micro-nutrient iron into the ocean. A rock weathering scheme is implemented into the model, with the weathering rate depending on lithology, runoff and soil temperature. CLIMBER-X includes a simple representation of the methane cycle, with explicitly modelled natural emissions from land and the assumption of a constant residence time of CH4 in the atmosphere. Carbon isotopes 13C and 14C are tracked through all model compartments and provide a useful diagnostic for model-data comparison. A comprehensive evaluation of the model performance for present–day and the historical period shows that CLIMBER-X is capable of realistically reproducing the historical evolution of atmospheric CO2 and CH4, but also the spatial distribution of carbon on land and the 3D structure of biogeochemical ocean tracers. The analysis of model performance is complemented by an assessment of carbon cycle feedbacks and model sensitivities compared to state-of-the-art CMIP6 models. Enabling interactive carbon cycle in CLIMBER-X results in a relatively minor slow-down of model computational performance by ~20 %, compared to a throughput of ~10,000 simulation years per day on a single node with 16 CPUs on a high performance computer in a climate–only model setup. CLIMBER-X is therefore well suited to investigate the feedbacks between climate and the carbon cycle on temporal scales ranging from decades to 〉100,000 years.

Description: Loess sediments are windblown silt deposits with, in general, a carbonate grain content of up to 30%. While regionally, loess was reported to increase weathering fluxes substantially, the influence on global weathering fluxes remains unknown. Especially on glacial-interglacial time scales, loess weathering fluxes might have contributed to land-ocean alkalinity flux variability since the loess areal extent during glacial epochs was larger. To quantify loess weathering fluxes, global maps representing the loess distribution were compiled. Water chemistry of rivers draining recent loess deposits suggests that loess contributes over-proportionally to alkalinity concentrations if compared to the mean of alkalinity concentrations of global rivers (~4,110 µeq L−1 for rivers draining loess deposits and ~1,850 µeq L−1 for the total of global rivers), showing comparable alkalinity concentration patterns in rivers as found for carbonate sedimentary rocks. Loess deposits, covering ~4% of the ice- and water-free land area, increase calculated global alkalinity fluxes to the coastal zone by 16%. The new calculations lead to estimating a 4% higher global alkalinity flux during the Last Glacial Maximum (LGM) compared to present fluxes. The effect of loess on that comparison is high. Alkalinity fluxes from silicate-dominated lithological classes were ~28% and ~30% lower during the LGM than recent (with loess and without loess, respectively), and elevated alkalinity fluxes from loess deposits compensated for this. Enhanced loess weathering dampens due to a legacy effect changes in silicate-dominated lithologies over the glacial-interglacial time scale.