10Be dating of North Pacific sediment cores up to 2.5 million years B.P.

The¹⁰Be method of dating of marine sediment cores is applied to five North Pacific cores. Assuming a constant¹⁰Be precipitation rate and varying sedimentation rates with time during the past 2.5 m.y. dating confirms to that obtained from paleomagnetic stratigraphy. The¹⁰Be concentration variations with depth in the cores are primarily due to changes in sediment dilution and do not reflect cosmic ray intensity or global climate variations. The limits of¹⁰Be deposition rate variation in the investigated cores are less than ± 10% for periods of (2–7) × 10⁵ years and less than ±30% for periods of 1 × 10⁵ years. The data set gives a half-life of¹⁰Be is 1.50 × 10⁶ years. The latitudinal effect of¹⁰Be concentrations and¹⁰Be/⁹Be ratios relates to a frequency of particulate matter occurrence (detrital and biological particles) in the oceans and to oceanic circulation.     

Transport ofBe andBe in the ocean

Beryllium isotopes (¹⁰Be and⁹Be) have been measured in suspended particles of < 1 mm size collected by mid-water sediment traps deployed in the eastern Pacific at MANOP sites H (6°32′N, 92°50′W, water depth 3600 m) and M (8°50′N, 104°00′W, 3100 m). For comparison, surface sediments from box cores taken from the two sites were also studied. The concentrations of¹⁰Be and⁹Be in sediment-trap particles are about an order of magnitude smaller than those in the bottom sediments which contain about 8 × 10⁹ and 6 × 10¹⁶ atoms g⁻¹ of¹⁰Be and⁹Be, respectively. The sediment trap samples collected from 50 m off the bottom showed significant (26–63%) contributions from resuspended bottom sediments. The¹⁰Be/⁹Be ratio in trap samples varies from 3 to 20 × 10⁻⁸. The variation may partly result from varied proportion of authigenic/detrital material. The fluxes of both isotopes exhibit a very strong seasonality. The fluxes of¹⁰Be into the traps at about 1500 m are estimated as 9 × 10⁵ and 4 × 10⁵ atoms cm⁻² a⁻¹ at sites H and M respectively. These values are to be compared with the fluxes into the sediments of 4–5 × 10⁵ atoms cm⁻² a⁻¹ at both locations. Good correlations exist between¹⁰Be,⁹Be and²⁷Al indicating that the primary carrier phase(s) for the beryllium isotopes in the water column may be aluminosilicates.     

The impact of storm-triggered landslides on sediment dynamics and catchment-wide denudation rates in the southern Central Range of Taiwan following the extreme rainfall event of Typhoon Morakot

Extreme erosion events can produce large short-term sediment fluxes. Such events complicate erosion rates estimated from cosmogenic nuclide concentrations in river sediment by providing sediment with a concentration different from the long-term basin average. We present a detrital ¹⁰Be study in southern Taiwan, with multiple samples obtained in a time sequence bracketing the 2009 Typhoon Morakot, to assess the impact of landslide sediment on ¹⁰Be concentrations (N¹⁰Be) in river sediment. Sediment samples were collected from 13 major basins, two or three times over the last decade, to observe the temporal variation of N¹⁰Be. Landslide inventories with time intervals of 5–6 years were used to quantify sediment flux changes. A negative correlation between N¹⁰Be and landslide areal density indicates dilution of N¹⁰Be by landslide sediment. Denudation rates estimated from the diluted N¹⁰Be can be up to three times higher than the lowest rate derived from the same basins. Observed increases imply that, 3 years after the passage of Typhoon Morakot, fluvial channels still contain a considerable amount of sediment provided by hillslope landslides during the event. However, higher N¹⁰Be in 2016 samples indicate that the contribution from landslide sediment at the sampled grain size has decreased with time. The correlation between changes in N¹⁰Be and landslide area and volume is not strong, likely resulting from the stochastic and complex nature of sediment transport. To simultaneously evaluate the volume of landslide-derived sediment and estimate the background denudation rate, associated with less impulsive sediment supply, we constructed a sediment-mixing model with the time series of N¹⁰Be and landslide inventories. The spatial pattern of background erosion rate in southern Taiwan is consistent with the regional tectonic framework, indicating that the landscape is evolving mainly in response to the tectonic forcing, and this signal is modified, but not obscured by impulsive sediment supply. © 2019 John Wiley & Sons, Ltd.     

Atmospherically-derived radionuclides as tracers of sediment mixing and accumulation in near-shore marine and lake sediments: Evidence from7Be,210Pb,and239,240Pu

Cosmogenic⁷Be(t_1/2 = 53.3days) has been used to estimate particle-mixing rates in the upper layers of lacustrine and near-shore marine sediments. Excess²¹⁰Pb and/or^239,240Pu have provided limits on rates of sediment accumulation in these environments and indices of the efficiency of the sediments as collectors of reactive nuclides over longer time scale.In sediment cores from Long Island Sound (marine) and Lake Whitney (fresh-water)⁷Be was measurable in the top 2–3 cm. Diffusion-analog particle-mixing coefficients calculated from these data are in the range of 10^?7 cm²/s. For Long Island Sound the coefficients are lower by factors of 3–6 than those estimated from the depth distributions of excess²³⁴Th at the same stations [14]. For Lake Whitney the calculated mixing coefficient is an upper limit because of the possibility of a sampling artifact.Measurements of total (wet + dry) atmospheric deposition of⁷Be in New Haven give an average flux of 0.07 dpm/cm² day during March-November, 1977; this is equivalent to a steady-state inventory of 5.4 dpm/cm² in a perfect collector. Sediment cores from Long Island Sound contain about half this⁷Be inventory, consistent with either a mean residence time for⁷Be in the water column of about one half-life or with post-depositional loss of⁷Be from Long Island Sound sediments. The Lake Whitney cores contain about 5 dpm/cm², much nearer the atmospheric delivery. A higher inventory of⁷Be in fresh-water, as compared to marine, sediments could be due either to a shorter mean residence time for⁷Be in fresh water or to lateral transport processes in the lake or its catchment. High inventories of excess²¹⁰Pb and^239,240Pu in Lake Whitney sediments demonstrate the importance of lateral transport on longer time scales at least.     

Distribution ofBe andBe in the Pacific Ocean

The vertical distributions of¹⁰Be and⁹Be at three locations in the Pacific (25°N, 170°E; 17°N, 118°W; 3°S, 117°W) are presented. The results show that both isotopes exhibit nutrient-like profiles. From the surface to the bottom, the increase for¹⁰Be is two- to threefold and that for⁹Be is about fivefold. While the inter-station variations in surface water concentrations may reach a factor of two, deep-water values tend to be much more uniform averaging about 2000 atoms/g for¹⁰Be and 30 pM for⁹Be. A similar situation applies to the¹⁰Be/⁹Be ratio; it varies approximately from 1 to 3 × 10⁻⁷ (atom/atom) at shallow depths but tends toward a value close to 1.1 × 10⁻⁷ in the deep ocean. The variation of¹⁰Be/⁹Be can be viewed as resulting from the fact that¹⁰Be in a given parcel of water consists of two components: recycled and primary. The recycled component is that part of¹⁰Be which has reached tracer equilibrium with⁹Be, as opposed to the primary component which, upon entering the sea from the atmosphere, has yet to equilibrate with⁹Be through particle cycling and mixing processes. It is estimated that 70% to nearly 100% of¹⁰Be at the three stations are being recycled, and the recycled beryllium bears an atomic ratio of¹⁰Be/⁹Be close to 1 × 10⁻⁷. The oceanic residence time of Be is of the order of 1000–4000 years, comparable to or slightly longer than the ocean mixing time.     

Greenland iceBe concentrations and average precipitation rates north of 40°N to 45°N

A model of¹⁰Be deposition within the subarctic and arctic is developed based on the behavior of⁹⁰Sr in the troposphere. Measured¹⁰Be fluxes, based on analyses of¹⁰Be in one year's snow fall (1979–1980) from the Dye-3 site in southwest Greenland and on published data, and predicted¹⁰Be fluxes, based on the¹⁰Be deposition model, agree. These results indicate that with regard to¹⁰Be, the troposphere north of 40°N to 45°N presently behaves as if it is well-mixed and that the average precipitation rate within that reservoir controls in large part the concentration of¹⁰Be in Greenland ice. Inversion of the Greenland ice core¹⁰Be concentration record with the aid of the model indicates: (1) that the average precipitation rate in the subarctic and arctic was lower than the present rate during the Maunder minimum of solar activity, and higher than the present rate during the Wolf and Sporer solar activity minimums; and (2) that during the Wisconsin-Holocene transition the average precipitation rate in the subarctic and arctic was about one third the present precipitation rate.     

Erosion of the eastern United States observed with 10Be

The problem of identifying areas of accelerated erosion in a dynamic landscape is complicated. The limited history of sediment yield measurements makes this task difficult even if geomorphic evidence is available. Beryllium-10, a cosmogenic isotope produced by cosmic rays interacting with the earth's atmosphere and surface, has chemical and physical properties that make it useful as a tracer for erosion and sediment transport processes. The rarity of the stable isotope, ⁹Be, allows ¹⁰Be to be detected with accelerator mass spectrometry in natural materials at extremely low levels. Backgrounds for rocks and sediments below 10⁵ atom per g are now attainable, a value to be compared with an average deposition rate of 1.3 × 10⁶ atom cm^?2 yr^?1. The affinity of Be for the components of soil and sediment is sufficiently high that it is effectively immobilized on contact, thereby allowing ¹⁰Be to function as a tracer of sediment transport. To a good approximation all the ¹⁰Be transport out of a drainage basin is on the sediment leaving it. The number of ¹⁰Be atoms passing the gauging station can be determined by measuring the concentration of the isotope in the sediment, if the annual sediment load is known. The ratio of the ¹⁰Be carried from the basin by the sediment to that incident upon it, called the erosion index, has been determined for 48 drainage basins within the same physiographic province, which allows them to be reasonably compared, all of which have sediment yield data. Basins located in the Atlantic coastal plain have an average index of 0.3 with the maximum observed being 0.9. Basins located between the fall line and the mountains, a region called the Piedmont, have an average value of 2.2 with individual values ranging from 0.6 to 6.7; this marked difference is thought to result from two centuries of farming on land of moderate gradient. Basins in the highland regions reflect local conditions with low indices for those in grass and timber and high indices associated with destructive land use. The data allow an estimate of the erosion index for the pre-colonial Piedmont, which then allows the pre-colonial sediment yield to be calculated. A number of basins have also been examined world wide with similar conclusions derived. An important deviation from the rule is noted for rivers that erode large regions of loess, such as the Mississippi, Hwang Ho, and Yangtze. Large aeolian deposits were laid down during the ice age in these basins, deposits that brought inherited ¹⁰Be with them and that are easily eroded.     

Be in a deep-sea core: implications regardingBe production changes over the past 420 ka

The influx of¹⁰Be into a globigerinid ooze core (CH72-02) from the eastern North Atlantic has been studied. This core contains a depositional record of the first 11 δ¹⁸O stages covering the last 423 ka. It is shown that the marine deposition of¹⁰Be is strongly influenced by the sedimentation of clays. Clay particles appear 10 times more efficient than the carbonate component as a carrier in bringing¹⁰Be to the bottom sediments. In core CH72-02, the deposition rates of¹⁰Be averaged over each oxygen-isotope stage for the past 11 stages show a scatter of ±40% about the mean value of 6.6 × 10⁸ atoms cm⁻² ka⁻¹. However, after correction for changes in lithology, the data show that the production rate of¹⁰Be over the same period has varied no more than ±25%, and the variations are not systematic in that high or low¹⁰Be production appear to be associated with either cold or warm climates. On the time scale of this investigation (intervals of ca. 50 ka over the last 420 ka, with resolutions as fine as 10 ka for portions of the record), it is unlikely that the shielding effect of the solar wind has deviated by more than ±25% or the geomagnetic field intensity has deviated by more than a factor of 1.6 from their long-term averages.     

Using in situ cosmogenic 10Be to identify the source of sediment leaving Greenland

We use the concentration of in situ ¹⁰Be in quartz isolated from fluvial and morainal sand to trace sediment sources and to determine the relative contribution of glacerized and deglaciated terrain to Greenland's sediment budget. We sampled along the western, eastern, and southern margins of the Greenland Ice Sheet, and collected sediment sourced from glacerized (n = 19) and non‐glacerized terrain (n = 10), from channels where sediment from glacerized and non‐glacerized terrain is mixed (n = 28), from Holocene glacial‐fluvial terraces (n = 4), and from one sand dune. In situ ¹⁰Be concentrations in sediment range from 1600 to 34 000 atoms g^‐1. The concentration of in situ ¹⁰Be in sediment sourced from non‐glacerized terrain is significantly higher than in sediment sourced from glacerized areas, in mixed channel sediment, and in terrace sediment that was deposited during the Holocene. To constrain the timing of landscape exposure for the deglaciated portion of the Narsarsuaq field area in southern Greenland, we measured in situ ¹⁰Be concentration in bedrock (n = 5) and boulder (n = 6) samples. Paired bedrock and boulder ages are indistinguishable at 1σ uncertainty and indicate rapid exposure of the upland slopes at ~10.5 ka. The isotope concentration in sediment sourced from non‐glacerized terrain is higher than in sediment sourced from glacerized terrain because the non‐glacerized landscape has been exposed to cosmic radiation since early Holocene deglaciation. Sediment from glacerized areas contains a low, but measurable concentration of ¹⁰Be that probably accumulated at depth during a prolonged period of exposure, probably before the establishment of the Greenland Ice Sheet. The concentration of ¹⁰Be in mixed fluvial sediment and in terrace sediment is low, and similar to the concentration in sediment from glacerized areas, which indicates that the Greenland Ice Sheet is the dominant source of sediment moving through the landscape outside the glacial margin in the areas we sampled. Copyright © 2014 John Wiley & Sons, Ltd.     

Aerosol deposition velocities on the Pacific and Atlantic oceans calculated from7Be measurements

The concentrations of⁷Be have been measured in Pacific and Atlantic ocean water for the past several years to determine the deposition velocity of aerosol particles on the ocean surface.⁷Be is produced at a relatively constant rate in the atmosphere by spallation reactions of cosmic rays with atmospheric nitrogen and oxygen. Immediately after its formation⁷Be becomes attached to aerosol particles, and therefore can serve as tracers of the subsequent behavior of these particles. Isopleths of⁷Be surface water concentrations,⁷Be inventory in the ocean, and deposition velocity have been prepared for the Pacific Ocean from 30°S to 60°N and for the Atlantic Ocean from 10°N to 55°N. The concentrations, inventories and deposition velocities tended to be higher in regions where precipitation was high, and generally increased with latitude. The average flux of⁷Be across the ocean surface was calculated to be 0.027 atoms cm^?2 s^?1 which is probably not significantly greater than the worldwide average⁷Be flux across land and ocean surfaces of 0.022 atoms cm^?2 s^?1 calculated by Lal and Peters. The average deposition velocity was calculated to be 0.80 cm s^?1. This value may be 10–50% too low, since it was calculated using atmospheric⁷Be concentrations which were measured at continental stations. Measurements of atmospheric⁷Be concentrations at ocean stations suggest that the concentrations at the continental stations averaged 10–50% higher than the concentrations over the ocean.     

Beryllium-10 in continental sediments

The concentration of¹⁰Be has been measured in 10 samples taken from a transect of surface sediments beginning in the Atchafalaya River and extending across the Bay 136 km into the Gulf of Mexico. If corrected for a lower retentivity of sand for Be, they have a concentration that is constant within 13%. This concentration is about an order of magnitude smaller than that of deep ocean sediments. For comparison, measurements of¹⁰Be in rainwater, in a sample of soil and in a deep ocean core were made.     

26Al/10Be ratios reveal the source of river sediments in the Kimberley,NW Australia

We use cosmogenic ¹⁰Be and ²⁶Al in both bedrock and fluvial sediments to investigate controls on erosion rates and sediment supply to river basins at the regional scale in the Kimberley, NW Australia. The area is characterised by lithologically controlled morphologies such as cuestas, isolated mesas and extensive plateaus made of slightly dipping, extensively jointed sandstones. All sampled bedrock surfaces at plateau tops, ridgelines, and in the broader floodplain of major rivers over the region show similar slow lowering rates between 0.17 and 4.88 m.Myr^-1, with a mean value of 1.0 ± 0.6 m.Myr^-1 (n=15), whilst two bedrock samples collected directly within river-beds record rates that are one to two orders of magnitude higher (14.4 ± 1.5 and 20.9 ± 2.5 m.Myr^-1, respectively). Bedrock ²⁶Al/¹⁰Be ratios are all compatible with simple, continuous sub-aerial exposure histories. Modern river sediment yield lower ¹⁰Be and ²⁶Al concentrations, apparent ¹⁰Be basin-wide denudation rates ranging between 1.8 and 7.7 m.Myr^-1, with a median value of 2.6 m.Myr^-1, more than double the magnitude of bedrock erosion rates. ²⁶Al/¹⁰Be ratios of the sediment samples are lower than those obtained for bedrock samples. We propose that these depleted ²⁶Al/¹⁰Be ratios can largely be explained by the supply of sediment to river basins from the slab fragmentation and chemical weathering of channel gorge walls and plateau escarpments that result in diluting the cosmogenic nuclide concentration in river sediments measured at the basin outlets. The results of a mass-balance model suggest that ~60–90% of river sediment in the Kimberley results from the breakdown and chemical weathering of retreating vertical sandstone rock-walls in contrast to sediment generated by bedrock weathering and erosion on the plateau tops. This study emphasises the value of analysing two or more isotopes in basin-scale studies using cosmogenic nuclides, especially in slowly eroding post-orogenic settings. © 2019 John Wiley & Sons, Ltd.     

Constant denudation rates in a high alpine catchment for the last 6 kyrs

Terrestrial cosmogenic nuclides (TCN) have widely been used as proxies in determining denudation rates in catchments. Most studies were limited to samples from modern active streams, thus little is known about the magnitude and causes of TCN variability on millennial time scales. In this work we present a 6 kyrs long, high resolution record of ¹⁰Be concentrations (n = 18), which were measured in sediment cores from an alluvial fan delta at the outlet of the Fedoz Valley in the Swiss Alps. This record is paired with a 3‐year time series (n = 4) of ¹⁰Be measured in sediment from the active stream currently feeding this fan delta. The temporal trend in the ¹⁰Be concentrations after correction for postdepositional production of ¹⁰Be was found to be overall constant and in good agreement with the modern river ¹⁰Be concentration. The calculated mean catchment‐wide denudation rate amounts to 0.73 ± 0.18 mm yr^?1. This fairly constant level of ¹⁰Be concentrations can be caused by a constant denudation rate over time within the catchment or alternatively by a buffered signal. In this contribution we suggest that the large alluvial floodplain in the Fedoz Valley may act as an efficient buffer on Holocene time scales in which sediments with different ¹⁰Be signatures are mixed. Therefore, presumable variations in the ¹⁰Be signals derived from changes in denudation under a fluctuating Holocene climate are only poorly transferred to the catchment outlet and not recorded in the ¹⁰Be record. However, despite the absence of high frequency signals, we propose that the buffered and averaged ¹⁰Be signal could be meaningfully and faithfully interpreted in terms of long‐term catchment‐averaged denudation rate. Our study suggests that alluvial buffers play an important role in regulating the ¹⁰Be signal exported by some alpine settings that needs to be taken into account and further investigated. Copyright © 2016 John Wiley & Sons, Ltd.     

Fluvial dynamics and 14C-10Be disequilibrium on the Bolivian Altiplano

Determining sediment transfer times is key to understanding source-to-sink dynamics and the transmission of environmental signals through the fluvial system. Previous work on the Bolivian Altiplano applied the in situ cosmogenic ¹⁴C-¹⁰Be-chronometer to river sands and proposed sediment storage times of ~10–20 kyr in four catchments southeast of Lake Titicaca. However, the fidelity of those results hinges upon isotopic steady-state within sediment supplied from the source area. With the aim of independently quantifying sediment storage times and testing the ¹⁴C-¹⁰Be steady-state assumption, we dated sediment storage units within one of the previously investigated catchments using radiocarbon dating, cosmogenic ¹⁰Be-²⁶Al isochron burial dating, and ¹⁰Be-²⁶Al depth-profile dating. Palaeosurfaces appear to preserve remnants of a former fluvial system, which has undergone drainage reversal, reduction in catchment area, and local isostatic uplift since ~2.8 Ma. From alluvium mantling the palaeosurfaces we gained a deposition age of ~580 ka, while lower down fluvial terraces yielded ≤34 ka, and floodplains ~3–1 ka. Owing to restricted channel connectivity with the terraces and palaeosurfaces, the main source of channel sediment is via reworking of the late Holocene floodplain. Yet modelling a set of feasible scenarios reveals that floodplain storage and burial depth are incompatible with the ¹⁴C-¹⁰Be disequilibrium measured in the channel. Instead we propose that the ¹⁴C-¹⁰Be offset results from: (i) non-uniform erosion whereby deep gullies supply hillslope-derived debris; and/or (ii) holocene landscape transience associated with climate or human impact. The reliability of the ¹⁴C-¹⁰Be chronometer vitally depends upon careful evaluation of sources of isotopic disequilibrium in a wide range of depositional and erosional landforms in the landscape. © 2018 John Wiley & Sons, Ltd.     

Differences in 10Be concentrations between river sand,gravel and pebbles along the western side of the central Andes

Cosmogenic nuclides in river sediment have been used to quantify catchment-mean erosion rates. Nevertheless, variable differences in ¹⁰Be concentrations according to grain size have been reported. We analyzed these differences in eleven catchments on the western side of the Andes, covering contrasting climates and slopes. The data include eight sand (0.5–1 mm) and gravel (1–3 cm) pairs and twelve sand (0.5–1 mm) and pebble (5–10 cm) pairs. The difference observed in three pairs can be explained by a difference in the provenance of the sand and coarser sediment. The other sand–pebble pairs show a lower ¹⁰Be concentration in the pebbles, except for one pair that shows similar concentrations. Two sand–gravel pairs show a lower ¹⁰Be concentration in the gravel and the other five pairs show a higher ¹⁰Be concentration in the gravel. Differences in climate do not reveal a particular influence on the ¹⁰Be concentration between pairs. The analysis supports a model where pebbles and gravel are mainly derived from catchment areas that are eroding at a faster rate. The five gravel samples with high ¹⁰Be concentrations probably contain gravel that were derived from the abrasion of cobbles exhumed at high elevations. In order to validate this model, further work should test if pebbles are preferentially exhumed from high erosion rate areas, and if the difference between pebbles with high ¹⁰Be concentrations and sand decreases when the erosion rate tends to be homogeneous within a catchment.     

The origin ofBe in island-arc volcanic rocks

The presence of cosmogenic¹⁰Be (t_1/2 = 1.5 × 10⁶ y) in island-arc volcanic rocks has been interpreted as indicating that sediments are subducted to the depths of island-arc magma genesis [1,2]. We have measured¹⁰Be and⁹Be (the stable common isotope) in phenocryst and groundmass fractions separated from four Aleutian volcanic rocks.¹⁰Be and⁹Be covary linearly in three of the rocks proving that the¹⁰Be was incorporated prior to the formation of phenocrysts. In the other rock¹⁰Be and⁹Be do not covary; the lack of covariation indicates either that the rock incorporated¹⁰Be during weathering or that⁹Be-rich xenocrysts were incorporated by mechanical mixing. Our results strongly support the hypothesis of Brown et al. [1] and Tera et al. [2] that sediments containing¹⁰Be are an integral part of island-arc magmatic systems. As we cannot identify the depth at which the¹⁰Be was incorporated we still cannot completely rule out the possibility of assimilation of sediments or altered crust near the Earth's surface as a source of¹⁰Be.     

Tracking denudation and sediment production and transport with cosmogenic 10Be in arid,high-altitude Himalayan half-grabens,Zanskar, northern India

Understanding the extent to which local factors, including bedrock and structure, govern catchment denudation in mountainous environments as opposed to broader climate or tectonic patterns provides insight into how landscapes evolve as sediment is generated and transported through them, and whether they have approached steady-state equilibrium. We measured beryllium-10 (¹⁰Be) concentrations in 21 sediment samples from glaciated footwall and hanging wall catchments, including a set of nested catchments, and 12 bedrock samples in the Puga and Tso Morari half-grabens located in the high-elevation, arid Zanskar region of northern India. In the Puga half-graben where catchments are underlain by quartzo-feldspathic gneissic bedrock, bedrock along catchment divides is eroding very slowly, about 5 m/Ma, due to extreme aridity and ¹⁰Be concentrations in catchment sediments are the highest (~60–90 × 10⁵ atoms/g SiO₂) as colluvium accumulates on hillslopes, decoupled from their ephemeral streams. At Puga, ¹⁰Be concentrations and the average erosion rates of a set of six nested catchments demonstrate that catchment denudation is transport-limited as sediment stagnates on lower slopes before reaching the catchment outlet. In the Tso Morari half-graben, gneissic bedrock is also eroding very slowly but ¹⁰Be concentrations in sediments in catchments underlain by low grade meta-sedimentary rocks, are significantly lower (~10–35 × 10⁵ atoms/g SiO₂). In these arid, high-elevation environments, ¹⁰Be concentrations in catchment sediments have more to do with bedrock weathering and transport times than steady-state denudation rates. © 2020 John Wiley & Sons, Ltd.     

Effects of sediment mixing on 10Be concentrations in the Zielbach catchment,central-eastern Italian Alps

Basin-wide erosion rates can be determined through the analysis of in situ-produced cosmogenic nuclides. In transient landscapes, and particularly in mountain catchments, erosion and transport processes are often highly variable and consequently the calculated erosion rates can be biased. This can be due to sediment pulses and poor mixing of sediment in the stream channels. The mixing of alluvial sediment is one of the principle conditions that need to be verified in order to have reliable results. In this paper we perform a field-based test of the extent of sediment mixing for a ∼42 km² catchment in the Alps using concentrations of river-born ¹⁰Be. We use this technique to assess the mechanisms and the spatio-temporal scales for the mixing of sediment derived from hillslopes and tributary channels. The results show that sediment provenance and transport, and mixing processes have a substantial impact on the ¹⁰Be concentrations downstream of the confluence between streams and tributary channels. We also illustrate that the extent of mixing significantly depends on: the sizes of the catchments involved, the magnitude of the sediment delivery processes, the downstream distance of a sample site after a confluence, and the time since the event occurred. In particular, continuous soil creep and shallow landsliding supply high ¹⁰Be concentration material from the hillslope, congruently increasing the ¹⁰Be concentrations in the alluvial sediment. Contrariwise, a high frequency of mass-wasting processes or the occurrence of sporadic but large-magnitude events results in the supply of low-concentration sediment that lowers the cosmogenic nuclide concentration in the channels. The predominance of mass-wasting processes in a catchment can cause a strong bias in detrital cosmogenic nuclide concentrations, and therefore calculated erosion rates may be significantly over- or underestimated. Accordingly, it is important to sample as close as possible to the return-period of large-size sediment input events. This will lead to an erosion rate representative of the “mass-wasting signal” in case of generally high-frequency events, or the “background signal” when the event is sporadic. Our results suggest that a careful consideration of the extent of mixing of alluvial sediment is of primary importance for the correct estimation of ¹⁰Be-based erosion rates in mountain catchments, and likewise, that erosion rates have to be interpreted cautiously when the mixing conditions are unknown or mixing has not been achieved.     

Topographic variation in soil erosion and accumulation determined with meteoric 10Be

Understanding natural soil redistribution processes is essential for measuring the anthropogenic impact on landscapes. Although meteoric beryllium-10 (¹⁰Be) has been used to determine erosion processes within the Pleistocene and Holocene, fewer studies have used the isotope to investigate the transport and accumulation of the resulting sediment. Here we use meteoric ¹⁰Be in hilltop and valley site soil profiles to determine sediment erosion and deposition processes in the Christina River Basin (Pennsylvania, USA). The data indicate natural erosion rates of 14 to 21 mm 10⁻³ yr and soil ages of 26 000 to 57 000 years in hilltop sites. Furthermore, valley sites indicate an alteration in sediment supply due to climate change (from the Pleistocene to the Holocene) within the last 60 000 years and sediment deposition of at least 0.5–2 m during the Wisconsinan glaciation. The change in soil erosion rate was most likely induced by changes in geomorphic processes; probably solifluction and slope wash during the cold period, when ice advanced into the mid latitudes of North America. This study shows the value of using meteoric ¹⁰Be to determine sediment accumulation within the Quaternary and quantifies major soil redistribution occurred under natural conditions in this region. © 2018 John Wiley & Sons, Ltd.     

Use of fallout radionuclides as indicators of erosion processes

The different depth penetration characteristics of ¹³⁷Cs, ⁷Be and ²¹⁰Pb excess in undisturbed soils can be used to identify erosion processes by analysis of sediments derived from surface erosion. Caesium-137 concentrations (half-life 30 years) typically decrease to half the surface value at between 30 and 50 mm. Beryllium-7 (half-life 53 days) has half-penetration depths of between 0.7 and 10 mm, whereas ²¹⁰Pb excess (half-life 20.2 years) has half-penetration depths between 10 and 30 mm. Experiments designed to determine the applicability of these depth penetration characteristics to soil erosion studies are reported. Surface runoff was artificially generated at two locations in a grazed paddock using a rainfall simulator. Suspended sediment was extracted from runoff and analysed for natural and artificial gamma emitting radio-nuclides. Suspended sediment derived from sheet flow contained initially high values of ¹³⁷Cs, ⁷Be and ²¹⁰Pb excess. As the experiment continued ¹³⁷Cs concentrations remained high, but ⁷Be and ²¹⁰Pb excess value decreased with time. This is interpreted as indicating a change from sheet dominated erosion to rill dominated erosion. During a second experiment artificial rain was allowed to fall onto an eroded gully wall. The derived suspended sediment contained no detectable ¹³⁷Cs, ⁷Be or ²¹⁰Pb excess. Overland flow from above the gully wall was then allowed to run down the gully face and mix with the water falling directly onto the gully wall. There was no detectable change in the radionuclide signature, showing that the gully wall was the predominant source of sediment. This was tested independently by mass balance and ²²⁶Ra to ²³²Th ratios. The good correlation between ²¹⁰Pb excess and ⁷Be at this site suggests that the differential technique described here may be applicable over time-scales longer than are possible with ⁷Be. It may therefore be practical to examine catchment erosion history through analysis of ²¹⁰Pb excess and ¹³⁷Cs in sediment cores.