Boron isotope fractionation in soils at Shale Hills CZO

Isotope fractionation of many elements can fingerprint the biogeochemical, weathering and erosion processes that govern the evolution of the Critical Zone (CZ). This study investigates boron isotope fractionation in two soil profiles developed on the same shale bedrock at Shale Hills Critical Zone Observatory. The first soil profile, located at the valley floor, is isotopically similar to the bedrock and appears to have lost boron mostly through the loss of fine particles matter (clays) with no isotopic fractionation. The second soil profile, located at the ridge top appears to be more depleted in boron concentration and isotopically fractionated toward lower values, as expected from mineral dissolution followed by adsorption/co-precipitation processes

Geological respiration of a mountain belt revealed by the trace element rhenium

Oxidation of rock-derived, petrogenic, organic carbon (OCpetro) during weathering of sedimentary rocks is a major source of carbon dioxide (CO2) to the atmosphere. This geological respiration is thought to be enhanced by physical erosion, suggesting that mountain belts could release large amounts of CO2 to counter the CO2 sequestration achieved by the erosion, riverine transfer and oceanic burial of organic carbon from the terrestrial biosphere. However, OCpetro oxidation rates in mountain belts have not been quantified. Here we use rhenium (Re) as a proxy to track OCpetro oxidation in mountain river catchments of Taiwan, where existing measurements of physical erosion rate allow the controls on OCpetro oxidation to be assessed. Re has been shown to be closely associated with OCpetro in rocks and following oxidation during chemical weathering forms a soluble oxyanion (View the MathML source) which contributes to the dissolved load of rivers. Soils on meta-sedimentary rocks in Taiwan show that Re loss is coupled to OCpetro loss during weathering, confirming previous observations from soil profiles on sedimentary rocks elsewhere. In Taiwan rivers, dissolved Re flux increases with the catchment-average sediment yield, suggesting that physical erosion rate is a major control on OCpetro oxidation. Based on our current understanding of Re mobility during weathering, the dissolved Re flux can be used to quantify an upper bound on the OCpetro oxidation rate and the associated CO2 transfer. The estimated CO2 release from this mountain belt by OCpetro oxidation does not negate estimates of CO2 sequestration by burial of biospheric OC offshore. The findings are compared to OC transfers estimated for the Himalaya, where OCpetro oxidation in the mountain belt remains unconstrained. Together, these cases suggest that mountain building in the tropics can result in a net sink of OC which sequesters atmospheric CO2

Boron isotope fractionation in soils at Shale Hills CZO

Isotope fractionation of many elements can fingerprint the biogeochemical, weathering and erosion processes that govern the evolution of the Critical Zone (CZ). This study investigates boron isotope fractionation in two soil profiles developed on the same shale bedrock at Shale Hills Critical Zone Observatory. The first soil profile, located at the valley floor, is isotopically similar to the bedrock and appears to have lost boron mostly through the loss of fine particles matter (clays) with no isotopic fractionation. The second soil profile, located at the ridge top appears to be more depleted in boron concentration and isotopically fractionated toward lower values, as expected from mineral dissolution followed by adsorption/co-precipitation processes

Storm-induced precipitation variability control of long-term erosion

International audienceErosion is often treated as a continuous process, yet it occurs through discrete events such as floods and landslides of variable magnitude and periodicity. It has also long been expected to be strongly dependent on precipitation, however, the influence of temporal rainfall variability upon long-term evolution of landscapes remains unclear. Here we report high erosion rates (0.8 to ∼10 mmyr−1over ∼70 ka) estimated from paleovolcanic reconstructions across a steep rainfall gradient on Reunion Island, which show that long-term erosion rates are influenced by the cyclone-induced variability of precipitation. Geostatistical analysis of 30 years of daily rainfall records reveals that erosion rates are high where the local climate is the driest and where the difference in intensity between extreme rainfall events and prevailing precipitation is the strongest. This implies that the intrinsic variability of precipitation impacts landscape evolution not only through extreme meteorological events, but also through background rainfall-induced parameters such as humidity and dryness, which modulate the erosion threshold of the Earth’s Critical Zone

Abrupt sea surface pH change at the end of the Younger Dryas in the central sub-equatorial Pacific inferred from boron isotope abundance in corals (<i>Porites</i>)

The "δ¹¹B-pH" technique was applied to modern and ancient corals <i>Porites</i> from the sub-equatorial Pacific areas (Tahiti and Marquesas) spanning a time interval from 0 to 20.720 calendar years to determine the amplitude of pH changes between the Last Glacial Period and the Holocene. Boron isotopes were measured by Multi-Collector – Inductively Coupled Plasma Mass Spectrometry (MC-ICPMS) with an external reproducibility of 0.25&permil;, allowing a precision of about &plusmn;0.03 pH-units for pH values between 8 and 8.3. The boron concentration [B] and isotopic composition of modern samples indicate that the temperature strongly controls the partition coefficient K_<i>D</i> for different aragonite species. Modern coral δ¹¹B values and the reconstructed sea surface pH values for different Pacific areas match the measured pH expressed on the seawater scale and confirm the calculation parameters that were previously determined by laboratory calibration exercises. Most ancient sea surface pH reconstructions near Marquesas are higher than modern values. These values range between 8.19 and 8.27 for the Holocene and reached 8.30 at the end of the last glacial period (20.7 kyr BP). At the end of the Younger Dryas (11.50&plusmn;0.1 kyr BP), the central sub-equatorial Pacific experienced a dramatic drop of up to 0.2 pH-units from the average pH of 8.2 before and after this short event. Using the marine carbonate algorithms, we recalculated the aqueous <i>p</i>CO₂ to be 440&plusmn;25 ppmV at around 11.5 kyr BP for corals at Marquesas and ~500 ppmV near Tahiti where it was assumed that <i>p</i>CO₂ in the atmosphere was 250 ppmV. Throughout the Holocene, the difference in <i>p</i>CO₂ between the ocean and the atmosphere at Marquesas (Δ<i>p</i>CO₂) indicates that the surface waters behave as a moderate CO₂ sink or source (−53 to 20 ppmV) during El Niño-like conditions. By contrast, during the last glacial/interglacial transition, this area was a marked source of CO₂ (21 to 92 ppmV) for the atmosphere, highlighting predominant La Niña-like conditions. Such conditions were particularly pronounced at the end of the Younger Dryas with a large amount of CO₂ released with Δ<i>p</i>CO₂ of +185&plusmn;25 ppmV. This last finding provides further evidence of the marked changes in the surface water pH and temperature in the equatorial Pacific at the Younger Dryas-Holocene transition and the strong impact of oceanic dynamic on the atmospheric CO₂ content

Lithium isotopes in large rivers reveal the cannibalistic nature of modern continental weathering and erosion

The erosion of major mountain ranges is thought to be largely cannibalistic, recycling sediments that were deposited in the ocean or on the continents prior to mountain uplift. Despite this recognition, it has not yet been possible to quantify the amount of recycled material that is presently transported by rivers to the ocean. Here, we have analyzed the Li content and isotope composition (View the MathML source) of suspended sediments sampled along river depth profiles and bed sands in three of the largest Earth's river systems (Amazon, Mackenzie and Ganga–Brahmaputra rivers). The View the MathML source values of river-sediments transported by these rivers range from +5.3 to −3.6‰ and decrease with sediment grain size. We interpret these variations as reflecting a mixture of unweathered rock fragments (preferentially transported at depth in the coarse fraction) and present-day weathering products (preferentially transported at the surface in the finest fraction). Only the finest surface sediments contain the complementary reservoir of Li solubilized by water–rock interactions within the watersheds. Li isotopes also show that river bed sands can be interpreted as a mixture between unweathered fragments of igneous and sedimentary rocks. A mass budget approach, based on Li isotopes, Li/Al and Na/Al ratios, solved by an inverse method allows us to estimate that, for the large rivers analyzed here, the part of solid weathering products formed by present-day weathering reactions and transported to the ocean do not exceed 35%. Li isotopes also show that the sediments transported by the Amazon, Mackenzie and Ganga–Brahmaputra river systems are mostly sourced from sedimentary rocks (>60%) rather than igneous rocks. This study shows that Li isotopes in the river particulate load are a good proxy for quantifying both the erosional rock sources and the fingerprint of present-day weathering processes. Overall, Li isotopes in river sediments confirm the cannibalistic nature of erosion and weathering

Ecosystem controlled soil-rock p CO 2 and carbonate weathering – Constraints by temperature and soil water content

Carbonate dissolution in soil-groundwater systems depends dominantly on pH, temperature and the saturation state of the solution with respect to abundant minerals. The pH of the solution is, in general, controlled by partial pressure of CO2 (pCO2) produced by ecosystem respiration, which is controlled by temperature and water availability. In order to better understand the control of land temperature on carbonate weathering, a database of published spring water hydrogeochemistry was built and analysed. Assuming that spring water is in equilibrium with the soil-water-rock-atmosphere, the soil pCO2 can be back-calculated. Based on a database of spring water chemistry, the average soil-rock CO2 was calculated by an inverse model framework and a strong relationship with temperature was observed. The identified relationship suggests a temperature control on carbonate weathering as a result of variations in soil-rock pCO2, which is itself controlled by ecosystem respiration processes. The findings are relevant for global scale analysis of carbonate weathering and carbon fluxes to the ocean, because concentration of weathering products from the soil-rock-system into the river system in humid, high temperature regions, are suggested to be larger than in low temperature regions. Furthermore, results suggest that, in specific spring samples, the hydrochemical evolution of rain water percolating through the soil-rock complex can best be described by an open system with pCO2 controlled by the ecosystem. Abundance of evaporites and pyrite sources influence significantly the chemistry of spring water and corrections must be taken into account in order to implement the inverse model framework presented in this study. Annual surface temperature and soil water content were identified as suitable variables to develop the parameterization of soil-rock pCO2, mechanistically consistent with soil respiration rate findings

Chemical Weathering of Loess and Its Contribution to Global Alkalinity Fluxes to the Coastal Zone During the Last Glacial Maximum, Mid‐Holocene, and Present

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

High potential for weathering and climate effects of non-vascular vegetation in the Late Ordovician

It has been hypothesized that predecessors of today’s bryophytes significantly increased global chemical weathering in the Late Ordovician, thus reducing atmospheric CO2 concentration and contributing to climate cooling and an interval of glaciations. Studies that try to quantify the enhancement of weathering by non-vascular vegetation, however, are usually limited to small areas and low numbers of species, which hampers extrapolating to the global scale and to past climatic conditions. Here we present a spatially explicit modelling approach to simulate global weathering by non-vascular vegetation in the Late Ordovician. We estimate a potential global weathering flux of 2.8 (km3 rock) yr−1, defined here as volume of primary minerals affected by chemical transformation. This is around three times larger than today’s global chemical weathering flux. Moreover, we find that simulated weathering is highly sensitive to atmospheric CO2 concentration. This implies a strong negative feedback between weathering by non-vascular vegetation and Ordovician climate

Vanadium

International audienceVanadium (chemical symbol, V) is a d-block transition metal,silver in color, appearing in the first long period of the peri-odic table between titanium and chromium. Vanadium hastwo stable isotopes: 50V and 51V, with atomic abundance of0.25 % and 99.75 %, respectively. Vanadium has several oxidation forms (between 2+ and 5+). In the lithosphere, Voccurs as reducing V(III) form, whereas in oxidizing con- ditions V prevails under V(IV) form. Vanadium(II) is partic- ularly unstable in the environment. Vanadium(III) is more stable than V(II), but it is also gradually oxidized by the air or dissolved oxygen. Vanadium(V) is expected to be the prevailing form in waters exposed to atmospheric oxygen, whereas V(IV) may be present in reducing environments. Depending upon geometry and environment, V ionic radii vary between 36 pm and 79 pm. Vanadium has a high melting point of 1910 42 C and is a mildly incompatible, refractory,lithophile (siderophile in the iron core and chondrites) ele- ment. Vanadium has an electronegativity of 1.63 on the Pau- ling scale and displays a first ionization potential of 6.74 eV. More details can be found in Richards (2006) and Haynes (2015)