Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • German  (2)
Type of Publication
Consortium
Language
  • German  (2)
  • 1
    UID:
    (DE-101)1291565345
    Format: Online-Ressource
    Content: Clay weathering in shales is an important component of the global Li budget because Li is mobilized from Li-rich clay minerals and shale represents about one quarter of the exposed rocks on Earth. We investigate Li isotopes and concentrations to explore implications and mechanisms of Li isotopic fractionation in Shale Hills, a first-order catchment developed entirely on shale in a temperate climate in the Appalachian Mountains, northeastern USA. The Li isotopic compositions (δ7Li) of aqueous Li in stream water and groundwater vary between 14.5 and 40.0‰. This range is more than half that observed in rivers globally. The δ7Li of aqueous Li increases with increasing Li retention in secondary minerals, which is simulated using a box model that considers pore fluid advection to be the dominant transport process, silicate dissolution to be the source of Li to the pore fluid, and uptake of Li by kaolinite, Fe-oxides, and interlayer sites of clays to be the sinks. The simulations suggest that only those deep groundwaters with δ7Li values of ∼15‰ are explainable as steady state values; those fluids with δ7Li values 〉 18‰, especially near-surface waters, can only be explained as time-dependent, transient signals in an evolving system. Lithium is highly retained in the residual solid phase during chemical weathering; however, bulk soils (0.5 ± 1.2‰ (1 SD)) and stream sediments (0.3‰) have similar, or higher, δ7Li values compared to average bedrock (−2.0‰). This is attributed to preferential removal of clay particles from soils. Soil clays are isotopically depleted in 7Li (δ7Li values down to −5.2‰) compared to parental material, and δ7Li values correlate with soil Li concentration, soil pH, and availability of exchangeable sites for Li as a function of landscape position (valley floor versus ridge top). The strong depletion of Li and clay minerals in soils compared to bedrock is attributed at least partly to loss of Li through export of fine-grained clay particles in subsurface water flow. This process might be enhanced as the upper weathering zone of this catchment is highly fractured due to former periglacial conditions. The Li isotopic composition of vegetation is similar to soil clay and both are distinct from mobile catchment water (soil pore water, stream and groundwater). Extrapolating from this catchment means that subsurface particle loss from shales could be significant today and in the past, affecting isotopic signatures of soils and water. For example, clay transformations together with removal of clay particles before re-dissolution support weathering conditions that lead to a low aqueous Li flux but to high δ7Li values in water.
    In: In: EPIC3Geochimica et Cosmochimica Acta, 295, pp. 155-177
    In: Datenlieferant: Alfred Wegener Institute for Polar- and Marine Research (AWI): ePIC (electronic Publication Information Center)
    Language: German
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    UID:
    (DE-101)1291565353
    Format: Online-Ressource
    Content: To further develop boron isotopes as a tool for understanding shale weathering, we explored patterns of boron concentrations and isotopes across the forested Susquehanna Shale Hills Critical Zone Observatory (CZO). We present boron measurements for all watershed components that provided a foundation for examining water-rock interactions in a shale dominated watershed, including water compartments (e.g., precipitation, stream water, groundwater) and solid compartments (e.g., soil, bedrock, stream sediments, suspended load, and leaf litter). Results show boron isotopes (δ11B) in the bedrock (− 4.6‰) and soil (− 5.9 to - 4.2‰) were very similar. All waters were enriched in 11B by comparison: precipitation (7.2 to 22.6‰), stream (10.3 to 15.5‰), and groundwater (2.2 to 17.4‰). Modeling revealed that isotopic fractionation observed in the surface water and groundwater could mainly be explained by water-rock interactions including clay mineral dissolution (e.g., chlorite) and coprecipitation/adsorption processes (e.g., coatings on illite particles), likely in the near surface soils (~2 m deep). We found that leaching, the loss of boron from vegetation to stream water, plays a secondary role. Specifically, such leaching likely contributes the equivalent of 10 to 26% of the B fluxes from the watershed outlet. Boron mass balance between bedrock and precipitation inputs and the exported flux of dissolved and solid pools identified a “missing” isotopically light solid flux (δ11B of −12.2 ± 5.3‰ at ~4.4 ± 3.8 mol/ha/y of B; uncertainty reported as 2 SD). We did not sample any pool with this isotopic signature. Here our data suggest the composition of this pool is more likely related to precipitation of secondary clays rather than adsorption or (co)precipitation on Fe oxides. We propose two hypotheses to explain the missing light B pool: 1) a significant portion of the particles carrying the missing 10B are not sampled because they enter groundwater at depth and are transported out of the catchment under the stream; and/or 2) the inputs and outputs of boron are not operating at steady state in the catchment today, suggesting that the missing boron particles were lost in the past in proportions higher than today. When this B budget is paired with studies of δ26Mg and δ56Fe from Shale Hills, both of which also show missing isotopic pools, the pattern indicates a fundamental gap in understanding of shale weathering. We concluded that light B particles, presumably generated in the upper soils, are likely transported deep beneath the surface in the groundwater system or episodically in the past through riverine fluxes.
    In: In: EPIC3Chemical Geology, Elsevier, 559, pp. 119900
    In: Datenlieferant: Alfred Wegener Institute for Polar- and Marine Research (AWI): ePIC (electronic Publication Information Center)
    Language: German
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. Further information can be found on the KOBV privacy pages