Variability of natural and bomb-produced radionuclide distributions in abyssal red clay sediments

The nature of sedimentation and mixing are examined in abyssal red clay sediments from the North Central Pacific using three types of indicators: ²³⁰Th/²³²Th, organic¹⁴C, and¹³⁷Cs and ^239.240Pu.²³⁰Th/²³²Th analysed revealed that the clay sedimentation rate in three box cores collected within a 50 km radius was less than 1.0 mm/10³ yr. However, analyses of the organic carbon in thin layers of sediment revealed that radiocarbon was present much deeper in the cores (down to 20 cm) than was expected from the ²³⁰Th/²³²Th distribution. In addition, both the stratigraphy and inventory of radiocarbon was significantly different between box cores. The distributions and inventories of¹³⁷Cs and^239.240Pu were similar to that found for radiocarbon, further illustrating the spatial variability of radionuclides in oligotrophic North Pacific red clays. These data suggest that bioturbational processes are important for transporting organic carbon down into the sediment column.     

High resolution Thex stratigraphy of sediments from high-latitude areas (Norwegian Sea, Fram Strait)

We present data on the average sedimentation rates (ranging from 1.6 cm/kyr to 3 cm/kyr) for the last 300.000 years based on δ¹⁸O analyses of foraminifera in a core from the Norwegian Sea and ²³⁰Th_ex measurements in cores from the Norwegian Sea and the Fram Strait (Arctic Ocean). Furthermore, we relate ²³⁰Th_ex variations downcore to the various oxygen isotope stages. This correlation is tentatively interpreted as being a result of the paleoceanographic and paleoclimatic control of bioproductivity. It is shown that based on the average sedimentation rates and characteristic ²³⁰Th_ex variations carbonate-poor sediment cores from northern latitudes can be correlated.     

10Be and Th isotopes in manganese nodules and adjacent sediments: Nodule growth histories and nuclide behavior

The concentration profiles of ⁹Be, ¹⁰Be, ²³⁰Th, ²³²Th, ²³¹Pa (via ²²⁷Th) and ²³⁸U have been measured in three manganese nodules, one each from the North Pacific (A47-16(4)), the South Pacific (TF-5) and the Indian Ocean (R/V Vitiaz). In addition the ¹⁰Be concentration in deep water from the GEOSECS reoccupation station 500 of the North Pacific, and in ? cores raised from the manganese nodule field in the North Pacific have been measured. The ¹⁰Be concentration in nodule and seawater samples was measured by the accelerator masss spectrometric technique employing the Yale Tandem Van de Graaff accelerator.The concentrations of ¹⁰Be, ²³⁰Th_exc and ²³¹Pa_exc and ratios of ¹⁰Be/⁹Be and ²³⁰Th_exc/²³²Th all decrease with depth in the nodules. This decrease, interpreted in terms of nodule growth, yields “average” growth rates of a few millimeters per million years for the nodules. The growth rates of the nodules exhibit temporal variations, both on short time (～ 50,000 years) and long time (several million years) scales. Of the three nodules studied, only in TF-5 is the short-term average growth rate based on ²³⁰Th_exc in the top 0–0.5 mm the same as the long-term average rate based on Be isotope data for the 0.5–17 mm interval. For the other two nodules, the recent average growth rates based on²³⁰Th_exc data differ significantly from the long-term average growth rates based on Be isotopes. In A47-16(4) the ¹⁰Be based rate is less than the ²³⁰Th_exc rate and in R/V Vitiaz the ¹⁰Be based rate is greater than the ²³⁰Th_exc rate. This observation, coupled with measurable changes in growth rates even during the past few hundred thousand years, suggests, but does not prove, that the discordant growth rates deduced from ²³⁰Th_exc and ¹⁰Be profiles document changes in nodule growth rate with time rather than mixing effects on ²³⁰Th_exc profiles.The ¹⁰Be concentration in the GEOSECS North Pacific deep water is 6100±1200 atoms/g. This value coupled with the average surface ¹⁰Be/⁹Be ratio of North Pacific nodules predicts a ⁹Be concentration within the limits of measured values. The inventory of ¹⁰Be and ²³⁰Th_exc in the nodules is only ～ 10% of the total, the remaining being in sediments. The ¹⁰Be concentrations in the upper portions of two adjacent cores studied are nearly the same, but the deposition fluxes of both ¹⁰Be and ²³⁰Th based on ²³⁰Th dating vary by a factor of two. This difference is attributable to local redistribution of sediment at the time of deposition prior to accumulation.     

Estimates of particle flux and reworking at the deep-sea floor using234Th/238U disequilibrium

Because of high specific activities of excess²³⁴Th (t_1/2 = 24.1 days) on suspended particles in the deep sea, this nuclide is potentially an extremely sensitive indicator of particle inputs and dynamics at the seafloor. Measurements were made at two deep-sea sites in order to examine this potential. Inventories of excess²³⁴Th at a low-current hemipelagic mud site (3990 m) in the Panama Basin were～ 1.5 (September, ′81) and～ 2.5 (June, ′82) dpm/cm². The steady state fluxes to the seafloor calculated from these inventories are in rough agreement with radionuclide fluxes measured in sediment traps. Small-scale (～ 100m) spatial variability in inventories implies biologically significant heterogeneity in particle inputs. Sediment from the continental rise site in the northwest Atlantic (2800 m), a site with higher current velocities than the Panama Basin, had an inventory of～ 1.9dpm/cm². This inventory is also in rough agreement with predictions made on the basis of nearby sediment trap data. Particle mixing coefficients of～ 30cm²/yr calculated at the Pacific and Atlantic sites are similar to those in shallow water deposits but could reflect disturbance during handling. Based on²¹⁰Pb data from the Panama Basin, sediment from below～ 6cm is mixed at a rate～ 10 × slower than the near-surface sediment to a depth of at least 20 cm. Agreement between²³⁴Th predicted mixing rates at the Panama Basin site with²¹⁰Pb profiles and in-situ experiments with glass bead tracers implies that these rates are real. Although the diffusion of dissolved²³⁴Th into deep-sea sediments complicates interpretations,²³⁴Th_xs distributions in bottom sediments offer a useful adjunct to sediment traps for investigation of particle dynamics near the deep-sea floor.     

Characterization of organic matter in marine sediments to estimate age offset of bulk radiocarbon dating

Radiocarbon dating of Arctic marine sediment is often challenging due to the low availability of calcareous fossils. Consequently, bulk organic matter dating has at times been used to establish sediment core chronologies. Yet, radiocarbon dates based on bulk organic matter often appear to deviate vastly from dates based on fossils, mainly caused by input of allochthounous carbon, including terrigenous organic matter. In this study, we aim to examine the link between the composition of the bulk organic matter and the age offsets between the bulk radiocarbon dates and those obtained from calcareous foraminiferal tests. All samples are taken from the marine sediment core AMD14-204C from offshore Upernavik (eastern Baffin Bay). The radiocarbon dates for bulk organic matter are on average ∼3000 years older than the radiocarbon dates based on foraminifera, but with changing age offsets throughout the record. To investigate the cause of this age offset and its variations over time, we applied core scanning, X-ray Fluorescence analysis, stable isotopes, organic pyrolysis and microscopic organic petrology to examine the distribution and characterization of the organic matter. The results show that the older organic matter includes clastic input of reworked sedimentary rocks potentially originating from West Greenland and/or the Canadian Arctic Archipelago. Changes in the input of contemporary marine algal produced organic matter versus both terrigenous input and reworked ancient organic matter appear to control the age offsets between the bulk and foraminifera dates. A low Hydrogen Index and low δ¹³C_org values together with a high Oxygen Index, indicative of high influence of terrigenous organic matter, seem to correspond to samples with the largest age offsets; 1000–2000 years greater than in other samples. To examine the cause of the variations in the age offsets, a new quantification of the autochthonous organic matter as a fraction of the TOC was calculated. This shows that samples with the largest age offsets contained the lowest fraction (as low as ∼12%) of autochthonous organic matter in the TOC.     

Spatial variation of U-Th series radionuclides and trace metals in deep-sea manganese encrustations

A series of measurements to assess the spatial variability on a scale of a few centimeters of UTh series nuclides and trace metals in surface layers of deep-sea ferromanganese encrustations are reported here. Two samples, one from an Atlantic seamount and another from MANOP site S in the Pacific are reported.The inventories of²³⁰Th_exc cm^?2 and²³¹Pa_exc cm^?2 as well as the ratios of the inventories are seen to vary by large amounts in samples only a few centimeters apart. These observations infer that the fluxes of these radionuclides to small areas on the ferromanganese crust may also vary with time. No strong correlation between the radioisotope inventories and concentrations of various elements has been observed.     

Interpretation of the 231Pa/230Th paleocirculation proxy: New water-column measurements from the southwest Indian Ocean

Measurements of ²³¹Pa, ²³⁰Th and ²³²Th concentrations have been made on five water-column profiles along the western margin of the Madagascar and Mascarene Basins in the southern Indian Ocean. These measurements help to fill a significant gap in the global coverage of water-column ²³²Th, ²³⁰Th and ²³¹Pa data. ²³²Th concentrations vary, but generally increase with depth, suggesting higher particle loading in deeper waters, and the presence of a significant dissolved fraction of ²³²Th. ²³⁰Th concentrations increase with depth, and profiles are similar to the average of existing data from other regions. ²³¹Pa concentrations, on the other hand, show significant depth structure, apparently reflecting the various water masses sampled at this location. The modified remnants of North Atlantic Deep Water are found at a depth of ≈ 2000 m and exhibit elevated ²³¹Pa concentrations exported from the South Atlantic. Antarctic Intermediate and Bottom Waters have lower ²³¹Pa, probably due to scavenging onto opal particles during transit from the Southern Ocean. The differences between water masses raises a question: which water mass is important in controlling the ²³¹Pa/²³⁰Th ratio in underlying sediments? A simple one-dimensional model is used to demonstrate that the ²³⁰Th and ²³¹Pa exported to sea-floor sediments last equilibrates with waters close to the seafloor (within ≈ 1000 m), rather than averaging the whole water column. These findings suggest that ²³¹Pa_xs/²³⁰Th_xs in sediments provides information primarily about deep-water masses. In this region, sedimentary records will therefore provide information about the past flow of Antarctic Bottom Water into the Indian Ocean. Interpretation of data from other regions, such as the North Atlantic where this proxy has most successfully been applied, requires careful consideration of regional oceanography and knowledge of the composition of the water masses being investigated.     

Assessing the importance of tropical cyclones on continental margin sedimentation in the Mississippi delta region

Recent research on the Mississippi margin indicates notable seasonal variation in seabed dynamics. During years with minimal tropical-system activity, sediments initially deposited from late spring to early fall are remobilized by wind-driven currents and wave energy during extra-tropical weather systems in the winter. This research reveals the profound significance of tropical cyclones on Louisiana Shelf sedimentation. The amount of material delivered to and advected across the shelf by recent tropical cyclones is considerably larger than that related to winter storm systems. In Fall 2004, the river-dominated shelf of Louisiana was impacted by three tropical systems in less than a month, including Hurricane Ivan. Ivan, with maximum sustained winds in excess of 74 m s⁻¹ (144 knots) and a minimum measured central pressure of 910 mbar, was the eighth most intense Atlantic hurricane on record at the time. In order to assess the impact these tropical systems had on the continental margin west of the Mississippi delta, seabed samples were collected from box cores in October 2004 and analyzed for particle-reactive radionuclides ²³⁴Th, ⁷Be, and ²¹⁰Pb. Radiochemical data and observations from X-radiographs indicate event-driven sediment deposits ranged from 4 to 30 cm on the shelf and 2–6 cm in the Mississippi Canyon. These deposits exhibit distinct radiochemical signatures and differ visually and texturally from the underlying sediment. The well-developed physical stratification and graded nature of the deposits observed in core X-radiographs suggests that the sediment could have been deposited from sediment-gravity flows. Inventories of ⁷Be and ⁷Be/²³⁴Th_xs ratios reveal this series of cyclones transported considerably more material to the outer shelf and slope than periods of minimal tropical-system activity. When compared to seasonal depositional rates created by winter storms, tropical-cyclone-related event deposits on the middle and outer shelf are up to an order of magnitude greater in thickness. The number and thickness of these event deposits decrease with distance from the delta and suggest that only the most severe tropical systems are likely capable of redistributing significant quantities of sediment to more distal portions of the shelf and slope. These severe-event-driven deposits may account for as much as 75% of the sediment burial budget on decadal time scales within Mississippi Canyon. Higher than average tropical cyclone activity, predicted by the National Hurricane Center over the next decade, may be the major mechanism controlling sediment transport and deposition on the Mississippi River continental shelf and in Mississippi Canyon.     

In-phase anomalies in Beryllium-10 production and palaeomagnetic field behaviour during the Iceland Basin geomagnetic excursion

Increases in the production rate of cosmogenic radionuclides associated with geomagnetic excursions have been used as global tie-points for correlation between records of past climate from marine and terrestrial archives. We have investigated the relative timing of variations in ¹⁰Be production rate and the corresponding palaeomagnetic signal during one of the largest Pleistocene excursions, the Iceland Basin (IB) event (ca. 190 kyr), as recorded in two marine sediment cores (ODP Sites 1063 and 983) with high sedimentation rates. Variations in ¹⁰Be production rate during the excursion were estimated by use of ²³⁰Th_xs normalized ¹⁰Be deposition rates and authigenic ¹⁰Be/⁹Be. Resulting ¹⁰Be production rates are compared with high-resolution records of geomagnetic field behaviour acquired from the same discrete samples. We find no evidence for a significant lock-in depth of the palaeomagnetic signal in these high sedimentation-rate cores. Apparent lock-in depths in other cores may sometimes be the result of lower sample resolution. Our results also indicate that the period of increased ¹⁰Be production during the IB excursion lasted longer and, most likely, started earlier than the corresponding palaeomagnetic anomaly, in accordance with previous observations that polarity transitions occur after periods of reduced geomagnetic field intensity prior to the transition. The lack of evidence in this study for a significant palaeomagnetic lock-in depth suggests that there is no systematic offset between the ¹⁰Be signal and palaeomagnetic anomalies associated with excursions and reversals, with significance for the global correlation of climate records from different archives.     

Uranium and thorium series nuclides in oriented ferromanganese nodules: growth rates,turnover times and nuclide behavior

Three ferromanganese nodules handpicked from the tops of 2500 cm² area box cores taken from the north equatorial Pacific have been analysed for their U-Th series nuclides.²³⁰Th_exc concentrations in the surface 1–2 mm of the top side of the nodules indicate growth rates of 1.8–4.6 mm/10⁶ yr. In two of the nodules a significant discontinuity in the²³⁰Th_exc depth profile has been observed at ～0.3 m.y. ago, suggesting that the nodule growth has been episodic. The concentration profiles of²³¹Pa_exc (measured via²²⁷Th) yield growth rates similar to the²³⁰Th_exc data. The bottom sides of the nodules display exponential decrease of²³⁰Th_exc/²³²Th activity ratio with depth, yielding growth rates of 1.5–3.3 mm/10⁶ yr.The²³⁰Th_exc and²³¹Pa_exc concentrations in the outermost layer of the bottom face are significantly lower than in the outermost layer of the top face. Comparison of the extrapolated²³⁰Th_exc/²³²Th and²³⁰Th_exc/²³¹Pa_exc activity ratios for the top and bottom surfaces yields an “age” of (5?15) × 10⁴ yr for the bottom relative to the top. This “age” most probably represents the time elapsed since the nodules have attained the present orientation.The²¹⁰Pb concentration in the surface ～0.1 mm of the top side is in large excess over its parent²²⁶Ra. Elsewhere in the nodule, up to ～1 mm depth in both top and bottom sides,²¹⁰Pb is deficient relative to²²⁶Ra, probably due to²²²Rn loss. The absence of²¹⁰Pb_exc below the outermost layer of the top face rules out the possibility of a sampling artifact as the cause of the observed exponentially decreasing²³⁰Th_exc and²³¹Pa_exc concentration profiles. The flux of²¹⁰Pb_exc to the nodules ranges between 0.31 and 0.58 dpm/cm² yr. The exhalation rate of²²²Rn, estimated from the²²⁶Ra-²¹⁰Pb disequilibrium is ～570 dpm/cm² yr from the top side and >2000 dpm/cm² yr from the bottom side.²²⁶Ra is deficient in the top side relative to²³⁰Th up to ～0.5–1 mm and is in large excess throughout the bottom. The data indicate a net gain of²²⁶Ra into the nodule, corresponding to a flux of (24?46) × 10^?3 dpm/cm² yr. On a total area basis the gain of²²⁶Ra into the nodules is <20% of the²²⁶Ra escaping from the sediments. A similar gain of²²⁸Ra into the bottom side of the nodules is reflected by the high²²⁸Th/²³²Th activity ratios observed in the outermost layer in contact with sediments.     

Can channel banks be the dominant source of fine sediment in a UK river?: an example using 137Cs to interpret sediment yield and sediment source

Cultivated fields have been shown to be the dominant sources of sediment in almost all investigated UK catchments, typically contributing 85 to 95% of sediment inputs. As a result, most catchment management strategies are directed towards mitigating these sediment inputs. However, in many regions of the UK such as the Nene basin there is a paucity of sediment provenance data. This study used the caesium‐137 (¹³⁷Cs) inventories of lake and floodplain cores as well as the ¹³⁷Cs activities of present day sediment to determine sediment provenance. Sediment yields were also reconstructed in a small lake catchment. Low ¹³⁷Cs inventories were present in the lake and floodplain cores in comparison to the reference inventory and inventories in cores from other UK catchments. Caesium‐137 activities in the present day sediments were low; falling close to those found in the channel bank catchment samples. It was estimated that 60 to 100% of the sediment in the Nene originated from channel banks. Pre‐1963 sediment yields were approximately 11.2 t km^?2 yr^?1 and post‐1963 was approximately 11.9 t km^?2 yr^?1. The lack of increased sediment yield post‐1963 and low sediment yield is unusual for a UK catchment (where a yield of 28 to 51 t km^?2 yr^?1 is typical for a lowland agricultural catchment), but is explained by the low predicted contribution of sediment from agricultural topsoils. The high channel bank contribution is likely caused by the river being starved of sediment from topsoils, increasing its capacity to entrain bank material. The good agreement between the results derived using cores and recently transported sediments, highlight the reliability of ¹³⁷Cs when tracing sediment sources. However, care should be taken to assess the potential impacts of sediment particle size, sediment focusing in lakes and the possible remobilization of ¹³⁷Cs from sedimentary deposits. Copyright © 2016 John Wiley & Sons, Ltd.     

Removal of 230Th and 231Pa at ocean margins

Uranium, thorium and protactinium isotopes were measured in particulate matter collected by sediment traps deployed in the Panama Basin and by in-situ filtration of large volumes of seawater in the Panama and Guatemala Basins. Concentrations of dissolved Th and Pa isotopes were determined by extraction onto MnO₂ adsorbers placed in line behind the filters in the in-situ pumping systems.Concentrations of dissolved ²³⁰Th and ²³¹Pa in the Panama and Guatemala Basins are lower than in the open ocean, whereas dissolved ²³⁰Th/²³¹Pa ratios are equal to, or slightly greater than, ratios in the open ocean. Particulate ²³⁰Th/²³¹Pa ratios in the sediment trap samples ranged from 4 to 8, in contrast to ratios of 30 or more at the open ocean sites previously studied. Particles collected by filtration in the Panama Basin and nearest to the continental margin in the Guatemala Basin contained ²³⁰Th/²³¹Pa ratios similar to the ratios in the sediment trap samples. The ratios increased with distance away from the continent.Suspended particles near the margin show no preference for adsorption of Th or Pa and therefore must be chemically different from particles in the open ocean, which show a strong preference for adsorption of Th. Ocean margins, as typified by the Panama and Guatemala Basins, are preferential sinks for ²³¹Pa relative to ²³⁰Th. Furthermore, the margins are sinks for ²³⁰Th and, to a greater extent, ²³¹Pa transported by horizontal mixing from the open ocean.     

Effect of human‐controlled hydrological regime on the source,transport, and flux of particulate organic carbon from the lower Huanghe (Yellow River)

Evaluating the role of fluvial transfer of terrestrial organic carbon (OC) and subsequent burial in the global carbon cycle requires the sources and fluxes of fluvial OC to be assessed, which remains poorly constrained in the Huanghe (Yellow River). Here, we report the elemental, stable isotopic, and radiocarbon activity of particulate organic carbon (POC) sampled at the outlet of Huanghe in 2012–2013. We show that the Huanghe riverine POC can be explained by binary mixing of fossil (POC_fossil) and non‐fossil (POC_non‐fossil) components, the former may reach ~40% of the total POC. The Huanghe POC_non‐fossil is mostly sourced from C3 plants, with a mean residence time of c. 2200 years. The current human‐controlled hydrological regime strongly influenced the POC sources, transport modes, and fluxes. In 2012–2013, the Huanghe delivered 0.73 Tg (1 Tg = 10¹² g) of POC to the sea, and about 28% of the annual POC flux occurred within a short human induced flood event. Globally, the Huanghe should be one of the largest rivers in the transfer and re‐burial of fossil OC. However, the fate of Huanghe fossil OC is still unconstrained and needs to be further investigated. Copyright © 2015 John Wiley & Sons, Ltd.     

Application of 210Pbex inventories to measure net hillslope erosion at burned sites

Fallout radionuclides, including lead‐210 excess (²¹⁰Pb_ex), have been broadly and successfully used to quantify net hillslope sediment transport in agricultural, pastoral and forested landscapes but have only recently been applied in burned terrain. Quantifying post‐fire erosion is important because fires can amplify hillslope erosion, impacting terrestrial and aquatic habitat and water quality. However, we lack a basic understanding of the fate of ²¹⁰Pb_ex in fires. To address this knowledge gap, we collected over 400 soil samples from unburned, moderately and severely burned forested sites in central Idaho. We measured soil ²¹⁰Pb_ex content at stable reference and eroding sites and in mineral and organic soil components. At all sites, organic matter had the highest concentration of ²¹⁰Pb_ex, representing 30% to 73% of the total activity. At the severely and moderately burned sites, ²¹⁰Pb_ex reference inventories were lower by 58% and 41%, with about 40% less organic mass, relative to the unburned site. These results indicate that most ²¹⁰Pb_ex in our semi‐arid, forested sites was bound to organic matter, and that a substantial portion of this lead was lost due to forest fires. These losses likely occurred through volatilization and wind transport of smoke and ash. In the moderately burned site, ²¹⁰Pb_ex losses were more spatially variable, potentially due to spatially uneven fire intensity and effects. Despite equal percent losses of ²¹⁰Pb_ex, lower inventories at the burned sites produced lower calculated net erosion rates relative to the unburned site. Thus, given methodological uncertainties, ²¹⁰Pb_ex losses due to fire, and the subsequent sensitivity of calculated net erosion rates to these lower ²¹⁰Pb_ex inventories, we suggest this method should not be used in burned terrain to calculate absolute net erosion and deposition rates. However, within a given burned site, ²¹⁰Pb_ex inventories still provide useful information describing relative soil losses and storage across the landscape. Copyright © 2012 John Wiley & Sons, Ltd.     

The spatial distribution of sedimentary compounds and their environmental implications in surface sediments of Lake Khar Nuur (Mongolian Altai)

Lake sediments are valuable natural archives to reconstruct paleoclimate and paleoenvironmental changes which consist of inorganic and organic sediment compounds of allochthonous origin from the catchment and of autochthonous production in the lake. However, for robust paleo-reconstructions it is important to develop a better understanding about sedimentation processes, the origin of inorganic and organic sediment compounds and their distribution within the lake. In this context, modern process studies provide important insights, although environmental and anthropological changes can affect the spatial distribution of sediment compounds through time. Therefore, in this study the spatial distribution of grain size and geochemical proxies in 52 surface sediment samples from Lake Khar Nuur, a small high-altitude lake in the Mongolian Altai with a small and anthropogenically used hydrological catchment, is investigated. The results show a distinct sediment focussing in the two deep basins of the lake, which therefore act as accumulation zones. In those accumulation zones, total organic carbon (TOC), total nitrogen (N) and their isotopic composition (δ¹³C_TOC, δ¹⁵N) as well as n-alkanes indicate that organic sediment compounds are a mixture of both allochthonous and autochthonous origin. While the recent catchment vegetation consists of grasses/herbs and the shrub Betula nana (L.) with distinct differences in their n-alkane homologue patterns, those differences are not reflected in the sediment surface samples which rather indicates that grass-derived n-alkanes become preferentially incorporated in the lake. Extensive anthropogenic activity such as grazing and housing in the southern part of the catchment causes soil erosion which is well reflected by high TOC, N and sulphur (S) contents and ¹⁵N depleted δ¹⁵N values at the central southern shore, i.e. increased allochthonous sediment input by anthropogenically-induced soil erosion. Overall, the surface sediments of Lake Khar Nuur origin from allochthonous and autochthonous sources and are focussed in the accumulation zones of the lake, while their distribution is both environmentally and anthropogenically driven.     

High-frequency time-series of the dynamic sedimentation processes on the western shelf of the Mississippi River Delta

Multiple box cores were collected on the continental shelf in the Mississippi Deltaic Region adjacent to Southwest Pass and analyzed for particle reactive radionuclides ²³⁴Th and ⁷Be to examine seasonal sediment dynamics associated with variations of river discharge and hydrodynamics. Three stations located along a line west of Southwest Pass were cored and reoccupied in October, November, and December of 2003 and March, April, and May of 2004. High-frequency sampling (∼monthly) comparable to the short half-life of the radiotracers (²³⁴Th t_1/2=24.1 d; ⁷Be t_1/2=53.3) enabled us to isolate the relative influence that various forcing agents (river discharge, waves, currents) had on sediment inventories of ⁷Be and ²³⁴Th. In addition, the primary source of ⁷Be (fluvial) differs from ²³⁴Th (marine), providing further insight into processes affecting sediment transport and supply. Monthly ⁷Be inventories showed a significant positive relationship to river discharge (P=0.03) proximal to Southwest Pass. Sites further from Southwest Pass exhibited little to no relationship between ⁷Be inventories and river flow. At these sites, monthly ⁷Be inventories demonstrated a significant positive relationship with average wave orbital velocity (P<0.01). During our sampling period, the transport of ⁷Be-rich sediments to sites located on the middle to outer shelf were dependent on sea conditions not river discharge. Relatively high wave orbital velocities potentially allow particles to remain in suspension longer and travel further distances before initial deposition. In addition, ²³⁴Th inventories showed evidence of sediment focusing during periods of high wave orbital velocities.     

137Cs湖泊沉积年代学方法应用的局限——以Crawford湖为例

＾１３７Ｃｓ湖泊沉积年代学方法是测定现代湖泊沉积物沉积年代和沉积速率的重要同位素年代学方法之一。对加拿大Ｃｒａｗｆｏｒｄ湖采集的沉积孔柱内＾１３７Ｃｓ垂直分布的研究发现,该方法给出时的标有明显偏差。比较＾２１０Ｐｂ和纹层等年代方法的结果,其１９６３年时标蓄积峰值所在位置明显移向表层,而作为１９５４年时标的该核素出现蓄积的层位则远早于该年沉积物蓄积层位。研究还表明,孔柱中较高的间隙水含量、缺少足以吸     

Magnetic enhancement in wildfire‐affected soil and its potential for sediment‐source ascription

Intense rainfall following wildfire can cause substantial soil and sediment redistribution. With concern for the increasing magnitude and frequency of wildfire events, research needs to focus on hydrogeomorphological impacts of fire, particularly downstream fluxes of sediment and nutrients. Here, we investigate variation in magnetic enhancement of soil by fire in burnt eucalypt forest slopes to explore its potential as a post‐fire sediment tracer. Low‐frequency magnetic susceptibility values (χ_lf) of <10 µm material sourced from burnt slopes (c. 8·0–10·4 × 10^?6 m³ kg^?1) are an order of magnitude greater than those of <10 µm material derived from long‐unburnt areas (0·8 × 10^?6 m³ kg^?1). Susceptibility of anhysteretic remanent magnetization (χARM) and saturation isothermal remanent magnetization (SIRM) values are similarly enhanced. Signatures are strongly influenced by soil and sediment particle size and storage of previously burnt material in footslope areas. Whilst observations indicate that signatures based on magnetic enhancement show promise for post‐fire sediment tracing, problems arise with the lack of dimensionality in such data. Magnetic grain size indicators χ_fd%, χARM/SIRM and χ_fd/χARM offer further discrimination of source material but cannot be included in numerical unmixing models owing to non‐linear additivity. This leads to complications in quantitatively ascribing downstream sediment to source areas of contrasting burn severity since sources represent numerical multiples of each other, indicating the need to involve additional indicators, such as geochemical evidence, to allow a more robust discrimination. Copyright © 2005 John Wiley & Sons, Ltd.     

The sources and seasonal fluxes of particulate organic carbon in the Yellow River

The Yellow River transports a large amount of sediment and particulate organic carbon (POC), which is thought to mainly derive from erosion of the Chinese Loess Plateau (CLP). However, the compositions, sources and erosional fluxes of POC in the Yellow River remain poorly constrained. Here we combined measurements of mineralogy, total organic carbon content (OC_total), stable organic carbon isotopes (δ¹³C_org), radiocarbon (¹⁴C) activity of organic matter in bulk suspended sediments collected seasonally from the upper and middle Yellow River, to quantify the compositions and fluxes of the POC and to assess its sources (biospheric and petrogenic POC, i.e. POC_bio and POC_petro, respectively). The results showed that the POC loading of sediments was controlled by mineralogy, grain size and specific surface area of loess particles. The F_mod of POC (0.71 to 0.31) can be explained by mixing of POC_petro with modern and aged POC_bio. A binary mixing model based on the hyperbolic relationship of the F_mod and OC_total revealed a wide range of ages of POC_bio from 1300 to 11100 ¹⁴C years. Relative to the upstream station, the annual POC_bio and POC_petro fluxes in the Yellow River are more than doubled after it flows crossing the CLP within 35% drainage area gain, resulting in POC_bio and POC_petro yields of the CLP at 3.50 ± 0.59 and 0.48 ± 0.49 tC/km²/yr, respectively. POC flux seasonal variation revealed that monsoon rainfall exerts a first-order control on the export of both POC_bio and POC_petro from the CLP to the Yellow River, resulting in more than 90% of the annual POC exported during the monsoon season. Around one third of annual POC erosional flux was transported during a storm event period, highlighting the important role of extreme events in POC export in this large river. © 2020 John Wiley & Sons, Ltd.