ALBERT

Description: A substantial amount of the atmospheric carbon taken up on land through photosynthesis and chemical weathering is transported laterally along the aquatic continuum from upland terrestrial ecosystems to the ocean. So far, global carbon budget estimates have implicitly assumed that the transformation and lateral transport of carbon along this aquatic continuum has remained unchanged since pre-industrial times. A synthesis of published work reveals the magnitude of present-day lateral carbon fluxes from land to ocean, and the extent to which human activities have altered these fluxes. We show that anthropogenic perturbation may have increased the flux of carbon to inland waters by as much as 1.0 Pg C yr−1 since pre-industrial times, mainly owing to enhanced carbon export from soils. Most of this additional carbon input to upstream rivers is either emitted back to the atmosphere as carbon dioxide (~0.4 Pg C yr−1) or sequestered in sediments (~0.5 Pg C yr−1) along the continuum of freshwater bodies, estuaries and coastal waters, leaving only a perturbation carbon input of ~0.1 Pg C yr−1 to the open ocean. According to our analysis, terrestrial ecosystems store ~0.9 Pg C yr−1 at present, which is in agreement with results from forest inventories but significantly differs from the figure of 1.5 Pg C yr−1 previously estimated when ignoring changes in lateral carbon fluxes. We suggest that carbon fluxes along the land–ocean aquatic continuum need to be included in global carbon dioxide budgets.

Description: Terrestrial enhanced weathering, the spreading of ultramafic silicate rock flour to enhance natural weathering rates, has been suggested as part of a strategy to reduce global atmospheric CO2 levels. We budget potential CO2 sequestration against associated CO2 emissions to assess the net CO2 removal of terrestrial enhanced weathering. We combine global spatial data sets of potential source rocks, transport networks, and application areas with associated CO2 emissions in optimistic and pessimistic scenarios. The results show that the choice of source rocks and material comminution technique dominate the CO2 efficiency of enhanced weathering. CO2 emissions from transport amount to on average 0.5–3% of potentially sequestered CO2. The emissions of material mining and application are negligible. After accounting for all emissions, 0.5–1.0 t CO2 can be sequestered on average per tonne of rock, translating into a unit cost from 1.6 to 9.9 GJ per tonne CO2 sequestered by enhanced weathering. However, to control or reduce atmospheric CO2 concentrations substantially with enhanced weathering would require very large amounts of rock. Before enhanced weathering could be applied on large scales, more research is needed to assess weathering rates, potential side effects, social acceptability, and mechanisms of governance.

Description: The spatial distribution of subsurface parameters such as permeability are increasingly relevant for regional to global climate, land surface, and hydrologic models that are integrating groundwater dynamics and interactions. Despite the large fraction of unconsolidated sediments on Earth's surface with a wide range of permeability values, current global, high‐resolution permeability maps distinguish solely fine‐grained and coarse‐grained unconsolidated sediments. Representative permeability values are derived for a wide variety of unconsolidated sediments and applied to a new global map of unconsolidated sediments to produce the first geologically constrained, two‐layer global map of shallower and deeper permeability. The new mean logarithmic permeability of the Earth's surface is −12.7 ± 1.7 m2 being 1 order of magnitude higher than that derived from previous maps, which is consistent with the dominance of the coarser sediments. The new data set will benefit a variety of scientific applications including the next generation of climate, land surface, and hydrology models at regional to global scales.

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: Connections between glaciation, chemical weathering, and the global carbon cycle could steer the evolution of global climate over geologic time, but even the directionality of feedbacks in this system remain to be resolved. Here, we assemble a compilation of hydrochemical data from glacierized catchments, use this data to evaluate the dominant chemical reactions associated with glacial weathering, and explore the implications for long-term geochemical cycles. Weathering yields from catchments in our compilation are higher than the global average, which results, in part, from higher runoff in glaciated catchments. Our analysis supports the theory that glacial weathering is characterized predominantly by weathering of trace sulfide and carbonate minerals. To evaluate the effects of glacial weathering on atmospheric pCO2, we use a solute mixing model to predict the ratio of alkalinity to dissolved inorganic carbon (DIC) generated by weathering reactions. Compared with nonglacial weathering, glacial weathering is more likely to yield alkalinity/DIC ratios less than 1, suggesting that enhanced sulfide oxidation as a result of glaciation may act as a source of CO2 to the atmosphere. Back-of-the-envelope calculations indicate that oxidative fluxes could change ocean–atmosphere CO2 equilibrium by 25 ppm or more over 10 ky. Over longer timescales, CO2 release could act as a negative feedback, limiting progress of glaciation, dependent on lithology and the concentration of atmospheric O2. Future work on glaciation–weathering–carbon cycle feedbacks should consider weathering of trace sulfide minerals in addition to silicate minerals.

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: Rivers are a major source of nutrients, carbon and alkalinity to the global ocean. In this study, we firstly estimate pre-industrial riverine loads of nutrients, carbon and alkalinity based on a hierarchy of weathering and terrestrial organic matter export models, while identifying regional hotspots of the riverine exports. Secondly, we implement the riverine loads into a global ocean biogeochemical model to describe their implications for oceanic nutrient concentrations, net primary production (NPP) and air–sea CO2 fluxes globally, as well as in an analysis of coastal regions. Thirdly, we quantitatively assess the terrestrial origins and the long-term fate of riverine carbon in the ocean. We quantify annual bioavailable pre-industrial riverine loads of 3.7 Tg P, 27 Tg N, 158 Tg Si and 603 Tg C delivered to the ocean globally. We thereby identify the tropical Atlantic catchments (20 % of global C), Arctic rivers (9 % of global C) and Southeast Asian rivers (15 % of global C) as dominant suppliers of carbon for the ocean. The riverine exports lead to a simulated net global oceanic CO2 source of 231 Tg C yr−1 to the atmosphere, which is mainly caused by inorganic carbon (source of 183 Tg C yr−1) and by organic carbon (source of 128 Tg C yr−1) riverine loads. Additionally, a sink of 80 Tg C yr−1 is caused by the enhancement of the biological carbon uptake from dissolved inorganic nutrient inputs from rivers and the resulting alkalinity production. While large outgassing fluxes are simulated mostly in proximity to major river mouths, substantial outgassing fluxes can be found further offshore, most prominently in the tropical Atlantic. Furthermore, we find evidence for the interhemispheric transfer of carbon in the model; we detect a larger relative outgassing flux (49 % of global riverine-induced outgassing) in the Southern Hemisphere in comparison to the hemisphere's relative riverine inputs (33 % of global C inputs), as well as an outgassing flux of 17 Tg C yr−1 in the Southern Ocean. The addition of riverine loads in the model leads to a strong NPP increase in the tropical west Atlantic, Bay of Bengal and the East China Sea (+166 %, +377 % and +71 %, respectively). On the light-limited Arctic shelves, the NPP is not strongly sensitive to riverine loads, but the CO2 flux is strongly altered regionally due to substantial dissolved inorganic and organic carbon supplies to the region. While our study confirms that the ocean circulation remains the main driver for biogeochemical distributions in the open ocean, it reveals the necessity to consider riverine inputs for the representation of heterogeneous features in the coastal ocean and to represent riverine-induced pre-industrial carbon outgassing in the ocean. It also underlines the need to consider long-term CO2 sources from volcanic and shale oxidation fluxes in order to close the framework's atmospheric carbon budget.

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.