Description: Climate change affects the stability and erosion of high‐alpine rock walls above glaciers (headwalls) that deliver debris to glacier surfaces. Since supraglacial debris in the ablation zone alters the melt behaviour of the underlying ice, the responses of debris‐covered glaciers and of headwalls to climate change may be coupled. In this study, we analyse the beryllium‐10 (10Be)‐cosmogenic nuclide concentration history of glacial headwalls delivering debris to the Glacier d'Otemma in Switzerland. By systematic downglacier‐profile‐sampling of two parallel medial moraines, we assess changes in headwall erosion through time for small, well‐defined debris source areas. We compute apparent headwall erosion rates from 10Be concentrations ([10Be]), measured in 15 amalgamated medial moraine debris samples. To estimate both the additional 10Be production during glacial debris transport and the age of our samples we combine our field‐based data with a simple model that simulates downglacier debris trajectories. Furthermore, we evaluate additional grain size fractions for eight samples to test for stochastic mass wasting effects on [10Be]. Our results indicate that [10Be] along the medial moraines vary systematically with time and consistently for different grain sizes. [10Be] are higher for older debris, closer to the glacier terminus, and lower for younger debris, closer to the glacier head. Computed apparent headwall erosion rates vary between ~0.6 and 10.8 mm yr−1, increasing over a maximum time span of ~200 years towards the present. As ice cover retreats, newly exposed headwall surfaces may become susceptible to enhanced weathering and erosion, expand to lower elevations, and contribute formerly shielded bedrock of likely different [10Be]. Hence, we suggest that recently lower [10Be] reflect the deglaciation of the debris source areas since the end of the Little Ice Age.

Description: In glacial landscapes, systematic downglacier‐sampling of medial moraine debris holds the potential to assess changes in headwall erosion through time. Cosmogenic beryllium‐10 (10Be) concentrations within the medial moraines of Glacier d'Otemma, Switzerland, broadly increase downglacier and translate into increasing headwall erosion rates towards the present. These trends may reflect processes associated with the exposure of new bedrock surfaces across recently deglaciating source headwalls.

Description: European Research Council (ERC) H2020‐EU.1.1.

Description: https://doi.org/10.5880/GFZ.3.3.2021.007

Description: As reverse weathering has been shown to impact long-term changes in atmospheric CO2 levels, it is crucial to develop quantitative tools to reconstruct marine authigenic clay formation. We explored the potential of the beryllium (Be) isotope ratio (10Be/9Be) recorded in marine clay-sized sediment to track neoformation of authigenic clays. The power of such proxy relies on the orders-of-magnitude difference in 10Be/9Be ratios between continental Be and Be dissolved in seawater. On riverine and marine sediments collected along a Chilean margin transect we chemically extracted reactive phases and separated the clay-sized sediment fraction. We compare the riverine and marine 10Be/9Be ratio of this fraction. Moreover, we compare the elemental and mineralogical composition and the Nd and Sr-isotopic composition of these samples. 10Be/9Be ratios increase four-fold from riverine to marine sediment. We attribute this increase to the incorporation of Be high in 10Be/9Be from dissolved biogenic opal, which also serves as a Si-source for the precipitation of marine authigenic clays. 10Be/9Be ratios thus sensitively track reverse-weathering reactions forming marine authigenic clays.

Description: To determine the depositional age and the long-term delivery of meteoric 10Be (10Bem) to the Rio Bermejo floodplain (northern Argentina), we collected floodplain sediment samples at four locations identified as point bars of abandoned Rio Bermejo channels. We used a stainless-steel hand auger to collect sediment down to a maximum depth of ~5 m, or until refusal. For 10Bem and 9Bereac analysis, we extracted samples that integrated material from 0-20 cm below the surface, 20-50 cm, and regularly spaced 40 cm intervals for lower depths. We homogenized the material prior to packing into clean plastic bags. Sediment particle size distributions were measured on ~10 mg aliquots using a laser diffraction particle size analyzer (Horiba LA-950). The total reactive phase, including amorphous oxyhydroxides and crystalline oxide grain coatings, was extracted from the sediment samples using a procedure adapted from Wittmann et al. (2012, doi:10.1016/j.chemgeo.2012.04.031). 10Be was purified from the extracted material, spiked with a 9Be carrier solution containing 150 µg of 9Be, and packed into targets for AMS measurement at the University of Cologne Centre for Accelerator Mass Spectrometry (Cologne, Germany). 10Be/9Be measurements were normalized to the KN01-6-2 and KN01-5-3 standards (Dewald et al., 2013, doi:10.1016/j.nimb.2012.04.030) that are consistent with a 10Be half-life of 1.36 ± 0.07 x10 yrˉ¹ (Nishiizumi et al., 2007, doi:10.1016/j.nimb.2007.01.297). 10Bem was calculated from the normalized and blank-corrected 10Be/9Be ratios. The reported 1σ uncertainties include counting statistics and the uncertainties of both standard normalization and blank correction. Stable 9Be concentrations were measured on a separate aliquot of the sample solution using inductively coupled plasma optical emission spectroscopy (ICP-OES). Uncertainty of ICP-OES measurements was 5%. We used coarse quartz grain OSL analysis to determine depositional ages for each floodplain core. For OSL analysis, we collected light-sealed samples by driving an opaque tube into our floodplain cores at two select depths in each core. OSL measurements were performed using a Risø DA 15 OSL/TL reader equipped with a 90Sr beta irradiator (4.9 Gy/min). OSL signals were stimulated with blue LEDs (470 nm, 50 s, 125 ºC) and detected through an optical filter (U 340 Hoya). For each sample, 40 aliquots were measured using the single-aliquot regenerative dose (SAR) protocol (Murray and Wintle, 2000, doi:10.1016/S1350-4487(03)00053-2) for equivalent dose determination.