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1.
Determining the riverine carbon fluxes to oceans is critical for an improved understanding of C budgets and biogeochemical cycles (C, O) over a broad range of spatial and time scales. Among the particulate organic carbon (POC) involved in these fluxes, those yielded by sedimentary rocks (petrogenic POC: pPOC) remain somewhat uncertain as to their source on continental surfaces. Based on time series from long‐term observatories, we refine the POC and sediments flux of the Rhône River, one of the major tributaries to the Mediterranean Sea. Radiocarbon measurements on a set of riverine samples and forward modelling were used to (i) determine a modelled pPOC content and pPOC/POC ratio for each sample set, (ii) assess pPOC flux delivered to the NW Mediterranean Sea, and (iii) estimate the badlands contribution from the Durance catchment to both the pPOC and to sediment discharges. The weighted pPOC flux contributes up to 26% of the POC flux (145 Gg yr‐1) discharged into the Mediterranean Sea, whereas the weighted pPOC content reaches 0.31 wt%. Despite their low contributive surface area (0.2%), badlands provide, respectively, 12, 3.5 and 14% of the pPOC, POC and sediment fluxes to the Rhône River. Consequently, such rocks can be considered as a major source of pPOC and sediments for the NW Mediterranean Sea and potentially for oceans. We suggest that river‐dominated ocean margins, such as the Rhône River, with badlands in their catchment could export a significant amount of pPOC to the oceans. Copyright © 2018 John Wiley & Sons, Ltd.  相似文献   

2.
This work relates to the debate on the fossil organic carbon (FOC) input in modern environments and its possible implication for the carbon cycle, and suggests the use of Rock‐Eval 6 pyrolysis as a relevant tool for tracking FOC in such environments. Considering that such a delivery is mainly due to supergene processes affecting the continental surface, we studied organic matter in different reservoirs such as bedrocks, alterites, soils and rivers in two experimental catchments at Draix (Alpes de Haute Provence, France). Samples were subjected to geochemical (Rock‐Eval 6 pyrolysis) investigations and artificial bacterial degradations. After comparing the geochemical fingerprint of samples, geochemical markers of FOC were defined and tracked in the different reservoirs. Our results confirm the contribution of FOC in modern soils and rivers and display the various influences of weathering and erosional processes on the fate of FOC during its exchange between these pools. In addition, the contrasting behaviour of these markers upon the supergene processes has also highlighted the refractory or labile characters of the fossil organic matter (FOM). Bedrock to river fluxes, controlled by gully erosion, are characterized by a qualitative and quantitative preservation of FOM. Bedrock to alterite fluxes, governed by chemical weathering, are characterized by FOC mineralization without qualitative changes in deeper alterites. Alterite to soils fluxes, controlled by (bio)chemical weathering, are characterized by strong FOC mineralization and qualitative changes of FOM. Thus weathering and erosional processes induce different FOM evolution and affect the fate of FOC towards the global carbon cycle. In this study, gully erosion would involve maintenance of an ancient sink for the global carbon cycle, while (bio)chemical processes provide a source of CO2. Finally, this study suggests that Rock‐Eval 6 pyrolysis can be considered as a relevant tool for tracking FOC in modern environments. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

3.
Climate factors play critical roles in controlling chemical weathering, while chemically weathered surface material can regulate climate change. To estimate global chemical weathering fluxes and CO2 balance, it is important to identify the characteristics and driving factors of chemical weathering and CO2 consumption on the Tibetan Plateau, especially in glaciated catchments. The analysis of the hydro-geochemical data indicated that silicate weathering in this area was inhibited by low temperatures, while carbonate weathering was promoted by the abundant clastic rocks with fresh surfaces produced by glacial action. Carbonate weathering dominated the riverine solute generation (with a contribution of 58%, 51%, and 43% at the QiangYong Glacier (QYG), the WengGuo Hydrological Station (WGHS), and the lake estuary (LE), respectively). The oxidation of pyrite contributed to 35%, 42%, and 30% of the riverine solutes, while silicate weathering contributed to 5%, 6%, and 26% of the riverine solutes at the QYG, WGHS, and LE, respectively. The alluvial deposit of easily weathering fine silicate minerals, the higher air temperature, plant density, and soil thickness at the downstream LE in comparison to upstream and midstream may lead to longer contact time between pore water and mineral materials, thus enhancing the silicate weathering. Because of the involvement of sulfuric acid produced by the oxidation of pyrite, carbonate weathering in the upstream and midstream did not consume atmospheric CO2, resulting in the high rate of carbonate weathering (73.9 and 75.6 t km−2 yr−1, respectively, in maximum) and potential net release of CO2 (with an upper constraint of 35.6 and 35.2 t km−2 yr−1, respectively) at the QYG and WGHS. The above results indicate the potential of the glaciated area of the Tibetan Plateau with pyrite deposits being a substantial natural carbon source, which deserves further investigation.  相似文献   

4.
In humid, forested mountain belts, bedrock landslides can harvest organic carbon from above ground biomass and soil (OCmodern) while acting to refresh the landscape surface and turnover forest ecosystems. Here the impact of landslides on organic carbon cycling in 13 river catchments spanning the length of the western Southern Alps, New Zealand is assessed over four decades. Spatial and temporal landslide maps are combined with the observed distribution and measured variability of hillslope OCmodern stocks. On average, it is estimated that landslides mobilized 7.6 ± 2.9 tC km?2 yr?1 of OCmodern, ~30% of which was delivered to river channels. Comparison with published estimates of OCmodern export in river suspended load suggests additional erosion of OCmodern by small, shallow landslides or overland flow in catchments. The exported OCmodern may contribute to geological carbon sequestration if buried in sedimentary deposits. Landslides may have also contributed to carbon sequestration over shorter timescales (<100 years). 5.4 ± 3.0 tC km?2 yr?1 of the eroded OCmodern was retained on hillslopes, representing a net‐carbon sink following re‐vegetation of scar surfaces. In addition, it was found that landslides caused rapid turnover of the landscape, with rates of 0.3% of the surface area per decade. High rates of net ecosystem productivity were measured in this forest of 94 ± 11 tC km?2 yr?1, which is consistent with rapid landscape turnover suppressing ecosystem retrogression. Landslide‐OCmodern yields and rates of turnover vary between river catchments and appear to be controlled by gradients in climate (precipitation) and geomorphology (rock exhumation rate, topographic slope). Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

5.
Recently, researchers have recognized the significant role of small mountainous river systems in the transport of carbon from terrestrial environments to the ocean, and the scale of such studies have ranged from channel bed units to continents. In temperate zones, these mountain river systems commonly drain catchments that are largely forested. However, the magnitude of carbon export from rivers draining old‐growth redwood forests has not been evaluated to date. Old‐growth redwood stands support some of the largest quantities of biomass in the world, up to 350 000 Mg of stem biomass km‐2 and soil organic carbon can reach 46 800 Mg km‐2. In north coastal California, suspended sediment samples were collected at three gaging stations for two to four years on streams draining old‐growth redwood forests. Carbon content, determined through loss‐on‐ignition tests, was strongly correlated with turbidity, and continuous turbidity records from the gaging stations were used to estimate annual carbon exports of 1 · 6 to 4 · 2 Mg km‐2 yr‐1. These values, representing 13 to 33% of the suspended sediment load, are some of the highest percentages reported in the global literature. The fraction of organic carbon as part of the suspended sediment load decreased with discharge, but reached an asymptote of 5 to 10% at flows 10 to 20 times the mean annual flows. Although larger rivers in this region exhibit high sediment yields (up to 3600 Mg km‐2 yr‐1), mainly attributed to high rates of uplift, mass movement, and timber harvest, the small pristine streams in this study have sediment yields of only 8 to 100 Mg km‐2 yr‐1. Because the current extent of old‐growth redwood stands is less than 5% of its pre‐European‐settlement distribution, the present organic carbon signature in suspended sediment loads in this region is likely different from that in the early 20th century. Published 2015. This article is a U.S. Government work and is in the public domain in the USA.  相似文献   

6.
Erosion and the associated loss of carbon is a major environmental concern in many peatlands and remains difficult to accurately quantify beyond the plot scale. Erosion was measured in an upland blanket peatland catchment (0.017 km2) in northern England using structure-from-motion (SfM) photogrammetry, sediment traps and stream sediment sampling at different spatial scales. A net median topographic change of –27 mm yr–1 was recorded by SfM over the 12-month monitoring period for the entire surveyed area (598 m2). Within the entire surveyed area there were six nested catchments where both SfM and sediment traps were used to measure erosion. Substantial amounts of peat were captured in sediment traps during summer storm events after two months of dry weather where desiccation of the peat surface occurred. The magnitude of topographic change for the six nested catchments determined by SfM (mean value: 5.3 mm, standard deviation: 5.2 mm) was very different to the areal average derived from sediment traps (mean value: –0.3 mm, standard deviation: 0.1 mm). Thus, direct interpolation of peat erosion from local net topographic change into sediment yield at the catchment outlet appears problematic. Peat loss measured at the hillslope scale was not representative of that at the catchment scale. Stream sediment sampling at the outlet of the research catchment (0.017 km2) suggested that the yields of suspended sediment and particulate organic carbon were 926.3 t km–2 yr–1 and 340.9 t km–2 yr–1, respectively, with highest losses occurring during the autumn. Both freeze–thaw during winter and desiccation during long periods of dry weather in spring and summer were identified as important peat weathering processes during the study. Such weathering was a key enabler of subsequent fluvial peat loss from the catchment. © 2019 John Wiley & Sons, Ltd.  相似文献   

7.
Black marls form very extensive outcrops in the Alps and constitute some of the most eroded terrains, thus causing major problems of sedimentation in artificial storage systems (e.g. reservoirs) and river systems. In the experimental catchments near Draix (France), soil erosion rates have been measured in the past at the plot scale through a detailed monitoring of surface elevation changes and at the catchment scale through continuous monitoring of sediment yield in traps at basin outlets. More recently, erosion rates have been determined by means of dendrogeomorphic techniques in three monitored catchments of the Draix basin. A total of 48 exposed roots of Scots pine have been sampled and anatomical variations in annual growth rings resulting from denudation analysed. At the plot scale, average medium‐term soil erosion rates derived from exposed roots vary between 1·8 and 13·8 mm yr?1 (average: 5·9 mm yr?1) and values are significantly correlated with slope angle. The dendrogeomorphic record of point‐scale soil erosion rates matches very well with soil erosion rates measured in the Draix basins. Based on the point‐scale measurements and dendrogeomorphic results obtained at the point scale, a linear regression model involving slope angle was derived and coupled to high‐resolution slope maps obtained from a LiDAR‐generated digital elevation model so as to generate high‐resolution soil erosion maps. The resulting regression model is statistically significant and average soil erosion rates obtained from the areal erosion map (5·8, 5·2 and 6·2 mm yr?1 for the Roubine, Moulin and Laval catchments, respectively) prove to be well in concert with average annual erosion rates measured in traps at the outlet of these catchments since 1985 (6·3, 4·1 and 6·4 mm yr?1). This contribution demonstrates that dendrogeomorphic analyses of roots clearly have significant potential and that they are a powerful tool for the quantification and mapping of soil erosion rates in areas where measurements of past erosion is lacking. Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

8.
Spatial and temporal variability of hydrological responses affecting surface water dissolved organic carbon (DOC) concentrations are important for determining upscaling patterns of DOC export within larger catchments. Annual and intra‐annual variations in DOC concentrations and fluxes were assessed over 2 years at 12 sites (3·40–1837 km2) within the River Dee basin in NE Scotland. Mean annual DOC fluxes, primarily correlated with catchment soil coverage, ranged from 3·41 to 9·48 g m?2 yr?1. Periods of seasonal (summer–autumn and winter–spring) DOC concentrations (production) were delineated and related to discharge. Although antecedent temperature mainly determined the timing of switchover between periods of high DOC in the summer‐autumn and low DOC in winter‐spring, inter‐annual variability of export within the same season was largely dependent on its associated water flux. DOC fluxes ranged from 1·39 to 4·80 g m?2 season?1 during summer–autumn and 1·43 to 4·15 g m?2 season?1 in winter–spring.Relationships between DOC areal fluxes and catchment scale indicated that mainstem fluxes reflect the averaging of highly heterogeneous inputs from contrasting headwater catchments, leading to convergent DOC fluxes at catchment sizes of ca 100 km2. However, during summer–autumn periods, in contrast to winter–spring, longitudinal mainstem DOC fluxes continue to decrease, most likely because of increasing biological processes. This highlights the importance of considering seasonal as well as annual changes in DOC fluxes with catchment scale. This study increases our understanding of the temporal variability of DOC upscaling patterns reflecting cumulative changes across different catchment scales and aids modelling of carbon budgets at different stages of riverine systems. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

9.
Total organic carbon fluxes of the Red River system (Vietnam)   总被引：1，自引：0，他引：1       下载免费PDF全文
Riverine transport of organic carbon from terrestrial ecosystems to the oceans plays an important role in the global carbon cycle. The Red River is located in Southeast Asia where river discharge, sediment loads and fluxes of elements (carbon, nitrogen and phosphorus) associated with suspended solids have been dramatically altered over past decades as a result of reservoir impoundment and land use, population, and climate change. Dissolved organic carbon (DOC) and particulate organic carbon (POC) concentrations were measured monthly at four stations of the Red River system from January 2008 to December 2010. The results reveal that POC changed synchronically with total suspended solids (TSS) concentration and with the river discharge, whereas no clear trend was observed for DOC concentration. The mean value of total organic carbon (TOC = DOC + POC) flux in the delta of the Red River was 31.5 × 1013 ± 4.0 × 1013 MgC.yr?1 (range 27.9–35.8 × 1013 MgC.yr?1 which leads to a specific TOC flux of 2012 ± 255 kgC.km?2.yr?1 during this 2008–2010 period. About 80% of the TOC flux was transferred to the estuary during the rainy season as a consequence of the higher river water discharge. The high mean value of the POC:Chl‐a ratio (1585 ± 870 mgC.mgChl‐a?1) and the moderate C:N ratio (7.3 ± 0.1) in the water column system suggest that organic carbon in the Red River system is mainly derived from erosion and soil leaching in the basin. The effect of two new dam impoundments in the Red River was also observable with lower TOC fluxes in 2010 compared with 2008. Copyright © 2017 John Wiley & Sons, Ltd.  相似文献   

10.
Solute concentrations in streamflow typically vary systematically with stream discharge, and the resulting concentration–discharge relationships are important signatures of catchment biogeochemical processes. Solutes derived from mineral weathering often exhibit decreasing concentrations with increasing flows, suggesting dilution of a kinetically limited weathering flux by a variable flux of water. However, previous work showed that concentration–discharge relationships of weathering‐derived solutes in 59 headwater catchments were much weaker than this simple dilution model would predict. Instead, catchments behaved as chemostats, with rates of solute production and/or mobilization that were nearly proportional to water fluxes, on both event and interannual timescales. Here, we re‐examine these findings using data for a wider range of solutes from 2,186 catchments, ranging from ~10 to >1,000,000 km2 in drainage area and spanning a wide range of lithologic and climatic settings. Concentration–discharge relationships among this much larger set of larger catchments are broadly consistent with the previously described chemostatic behaviour, at least on event and interannual timescales for weathering‐derived solutes. Among these same catchments, however, site‐to‐site variations in mean concentrations of weathering‐derived solutes exhibit strong negative correlations with long‐term average precipitation and discharge, reflecting strong climatic control on long‐term leaching of the critical zone. We use multiple regression of site characteristics including discharge to identify potential controls on long‐term mean concentrations and find that lithologic and land cover controls are significant predictors for many analytes. The picture that emerges is one in which, on event and interannual timescales, weathering‐derived stream solute concentrations are chemostatically buffered by groundwater storage and fast chemical reactions, but each catchment's chemostatic “set point” reflects site‐to‐site differences in climatically driven evolution of the critical zone. In contrast to these weathering products, some nutrients and particulates are often near‐chemostatic across all timescales, and their long‐term mean concentrations correlate more strongly with land use than climatic characteristics.  相似文献   

11.
This study was undertaken to test the utility of a geographical information systems (GIS) approach to problems of watershed mass balance. This approach proved most useful in exploring the effects that watershed scale, lithology and land use have on chemical weathering rates, and in assessing whether mass balance calculations could be applied to large multilithological watersheds. Water quality data from 52 stations were retrieved from STORET and a complete GIS database consisting of the watershed divide, lithology and land use was compiled for each station. Water quality data were also obtained from 7 experimental watersheds to develop a methodology to estimate annual fluxes from incomplete data sets. The methodology consists of preparing a composite of daily flux data, calculating a best fit sinusoid and integrating the equation to obtain an annual flux. Comparison with annual fluxes calculated from high resolution data sets suggests that this method predicts fluxes within about 10% of the true annual flux. Annual magnesium fluxes (moles km−2 yr−1) were calculated for all stations and adjusted for fluxes from atmospheric deposition. Magnesium flux was found to be a strong function of the amount of carbonate in the watershed, and silica fluxes were found to increase with the fraction of sandstone present in the watershed. All fluxes were strongly influenced by mining practices, with magnesium fluxes from affected watersheds being 6–10 times higher than fluxes from comparable pristine watersheds. Mining practices enhance chemical weathering by increasing the surface area of unweathered rock to which water has access and by increasing acidity and rate of mineral weathering. Fluxes were also found to increase with watershed size. This scale dependence is most likely caused by the sensitivity of weathering fluxes to even minor quantities of carbonates, which are likely to be found in all lithologies at larger scales. Mass balances were carried out in watersheds where gauged sub-watersheds made up more than 95% of the area. The calculations show large magnesium flux and water balance discrepancies. These errors may be a result of significant groundwater inputs to streams between gauges. The results suggest that improvements in how we measure discharge and estimate fluxes may be required before we can apply mass balance techniques to larger scales. © 1997 John Wiley & Sons, Ltd.  相似文献   

12.
Dissolved major ions, Sr concentrations and 87Sr/86Sr ratios of 10 coastal lakes from the Larsemann Hills, East Antarctica have been studied to constrain their solute sources, transport and glacial weathering patterns in their catchments. In absence of perennial river/streams, lakes serve as only reliable archive to study land surface processes in these low-temperature regions. The lake water chemistry is mostly Na-Cl type and it does not show any significant depth variations. Sr isotope compositions of these lakes vary from 0.7110 to 0.7211 with an average value of 0.7145, which is higher than modern seawater value. In addition to oceanic sources, major ions and Sr isotopic data show appreciable amount of solute supply from chemical weathering of silicate rocks in lake catchments and dissolution of Ca-Mg rich salts produced during the freezing of seawaters. The role of sulphide oxidation and carbonate weathering are found to be minimal on lake hydro-chemistry in this part of Antarctica. Inverse model calculations using this chemical dataset provide first-order estimates of dissolved cations and Sr; they are mostly derived from oceanic (seawater + snow) sources (cations approximately 76%) and (Sr approximately 92%) with minimal supplies from weathering of silicates (cations approximately 15%); (Sr approximately 2%) and Ca-rich minerals (cations approximately 9%); (Sr approximately 7%). The silicate weathering rate and its corresponding atmospheric CO2 consumption rate estimates for Scandrett lake catchment (3.6 ± 0.3 tons/km2/year and 0.5 × 105 moles/km2/year), are lower than that of reported values for the average global river basins (5.4 tons/km2/year and 0.9 × 105 tons/km2/year) respectively. The present study provides a comprehensive report of chemical weathering intensity and its role in atmospheric CO2 consumption in low-temperature pristine environment of Antarctica. These estimates underscore the importance of Antarctica weathering on atmospheric CO2 budget, particularly during the past warmer periods when the large area was exposed and available for intense chemical weathering.  相似文献   

13.
Most hillslope studies examining the interplay between climate and earth surface processes tend to be biased towards eroding parts of landscapes. This limitation makes it difficult to assess how entire upland landscapes, which are mosaics of eroding and depositional areas, evolve physio‐chemically as a function of climate. Here we combine new soil geochemical data and published 10Be‐derived soil production rates to estimate variations in chemical weathering across two eroding‐to‐depositional hillslopes spanning a climate gradient in southeastern Australia. At the warmer and wetter Nunnock River (NR) site, rates of total soil (–3 to –14 g m‐2 yr‐1; negative sign indicates mass loss) and saprolite (–18 to –32 g m‐2 yr‐1) chemical weathering are uniform across the hillslope transect. Alternatively, the drier hillslope at Frog's Hollow (FH) is characterized by contrasting weathering patterns in eroding soils (–30 to –53 g m‐2 yr‐1) vs. depositional soils (+91 g m‐2 yr‐1; positive sign indicates mass addition). This difference partly reflects mineral grain size sorting as a result of upslope bioturbation coupled with water‐driven soil erosion, as well as greater vegetative productivity in moister depositional soils. Both of these processes are magnified in the drier climate. The data reveal the importance of linking the erosion–deposition continuum in hillslope weathering studies in order to fully capture the coupled roles of biota and erosion in driving the physical and chemical evolution of hillslopes. Our findings also highlight the potential limitations of applying current weathering models to landscapes where particle‐sorting erosion processes are active. Copyright © 2018 John Wiley & Sons, Ltd.  相似文献   

14.
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15.
Snowmelt‐fed springs and small (0.5 km2) upland catchments in alpine areas of the western United States contribute significantly to the quantity and inorganic chemistry of water delivered to downstream basins but have not been studied extensively. Mineral weathering, transit time, and hydrologic mixing control the solute chemistry of waters that drain the upland zone of Niwot Ridge, Colorado Front Range, and adjacent areas in the granitic core of the Southern Rocky Mountains. Water in 37 springs sampled in this study flows in generally short steep paths (~0.3 km) through shallow regolith with mean transit times (MTT) of weeks to months, producing solutions dominated by Si, Ca2+, Na+, and HCO3?, locally SO42?. Rock type is a significant control on spring, surface, and shallow groundwater chemistry, and plagioclase (oligoclase) is the major source of dissolved Na+ and Si. Concentrations of Ca2+ exceed stoichiometric predictions of oligoclase weathering by ~3.5×; excess Ca2+ likely represents weathering of aeolian material, vein calcite, or trace minerals. Concentrations of base cations and Si increase slowly with estimated MTT of 0.2 years for Niwot Ridge spring waters, and several years for shallow groundwater sampled by wells. Chemical weathering of silicate minerals is slow with estimated rates of ~2.0 and 0.2 pmol·m?2·s?1 for oligoclase and microcline, respectively; the most mineralized spring waters are saturated only with respect to kaolinite and montmorillonite. More than 50% of the dissolved base cations + Si measured in Boulder Creek at Orodell (~25 km downstream) accumulate before water emerges from alpine springs on Niwot Ridge. Warming global temperatures are shifting more high‐elevation precipitation to rain, potentially changing run‐off patterns, transit time, and solute loads. Acquisition of solutes by alpine waters thus has implications far beyond small upland catchments.  相似文献   

16.
Aga Nowak  Andy Hodson 《水文研究》2015,29(6):1588-1603
Our novel study examines landscape biogeochemical evolution following deglaciation and permafrost change in Svalbard by looking at the productivity of various micro‐catchments existing within one watershed. It also sheds light on how moraine, talus and soil environments contribute to solute export from the entire watershed into the downstream marine ecosystem. We find that solute dynamics in different micro‐catchments are sensitive to abiotic factors such as runoff volume, water temperature, geology, geomorphological controls upon hydrological flowpaths and landscape evolution following sea level and glacial changes. Biotic factors influence the anionic composition of runoff because of the importance of microbial SO42? and NO3? production. The legacy of glaciation and its impact upon sea level changes is shown to influence local hydrochemistry, allowing Cl? to be used as a tracer of thawing permafrost that has marine origins. However, we show that a ‘glacial signal’ dominates solute export from the watershed. Therefore, although climatically driven change in the proglacial area has an influence on local ecosystems, the biogeochemical response of the entire watershed is dominated by glacially derived products of rapid chemical weathering. Consequently, only the study of micro‐catchments existing within watersheds can uncover the landscape response to contemporary climate change. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

17.
Landscapes evolve in response to external forces, such as tectonics and climate, that influence surface processes of erosion and weathering. Internal feedbacks between erosion and weathering also play an integral role in regulating the landscapes response. Our understanding of these internal and external feedbacks is limited to a handful of field‐based studies, only a few of which have explicitly examined saprolite weathering. Here, we report rates of erosion and weathering in saprolite and soil to quantify how climate influences denudation, by focusing on an elevation transect in the western Sierra Nevada Mountains, California. We use an adapted mass balance approach and couple soil‐production rates from the cosmogenic radionuclide (CRN) 10Be with zirconium concentrations in rock, saprolite and soil. Our approach includes deep saprolite weathering and suggests that previous studies may have underestimated denudation rates across similar landscapes. Along the studied climate gradient, chemical weathering rates peak at middle elevations (1200–2000 m), averaging 112·3 ± 9·7 t km–2 y–1 compared to high and low elevation sites (46·8 ± 5·2 t km?2 y?1). Measured weathering rates follow similar patterns with climate as those of predicted silica fluxes, modeled using an Arrhenius temperature relationship and a linear relationship between flux and precipitation. Furthermore, chemical weathering and erosion are tightly correlated across our sites, and physical erosion rates increase with both saprolite weathering rates and intensity. Unexpectedly, saprolite and soil weathering intensities are inversely related, such that more weathered saprolites are overlain by weakly weathered soils. These data quantify exciting links between climate, weathering and erosion, and together suggest that climate controls chemical weathering via temperature and moisture control on chemical reaction rates. Our results also suggest that saprolite weathering reduces bedrock coherence, leading to faster rates of soil transport that, in turn, decrease material residence times in the soil column and limit soil weathering. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

18.
South Cameroon is located in a tropical and tectonically quiescent region, with landscapes characterized by thick highly weathered regolith, indicative of the long‐term predominance of chemical weathering over erosion. Currently this region undergoes huge changes due to accelerated mutations related to a growing population and economical developments with associated needs and increasing pressures on land and natural resources. We analysed two of the main south Cameroon rivers: the Nyong River and Sanaga River. The Sanaga catchment undergoes a contrasted tropical climate from sub‐humid mountainous and humid climate and is impacted by deforestation, agriculture, damming, mining and urbanization, especially in the Mbam sub‐basin, draining the highly populated volcanic highlands. By contrast, the Nyong catchment, only under humid tropical climate, is preserved from anthropogenic disturbance with low population except in the region of Yaoundé (Méfou sub‐basin). Moreover the Nyong basin is dam‐free and less impacted by agriculture and logging. We explore both denudation temporal variability and the ratio between chemical and physical denudation through two catchment‐averaged erosion and denudation datasets. The first one consists of an 11‐year long gauging dataset, while the second one comes from cosmogenic radionuclides [CRNs, here beryllium‐10 (10Be)] from sand sampled in the river mainstreams (timescale of tens to hundreds of thousands of years). Modern fluxes estimated from gauging data range from 5 to 100 m/Ma (10 to 200 t/km2/yr); our calculations indicate that the usual relative contribution of chemical versus physical denudation is 60% and 40%, respectively, of the total denudation. Beryllium‐10 denudation rates and sediment fluxes range from 4.8 to 40.3 m/Ma or 13 to 109 t/km2/yr, respectively, after correction for quartz enrichment. These fluxes are slightly less than the modern fluxes observed in Cameroon and other stable tropical areas. The highest 10Be‐derived fluxes and the highest physical versus chemical denudation ratios are attributed to anthropogenic impact. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

19.
Mass balance studies in forested catchments in the northeastern USA show that S losses via streamwater SO42? exceed measured atmospheric S inputs. Possible sources of the excess S loss include underestimated dry deposition, mineralization of organic S in soils, desorption of soil sulphate, oxidation of recently formed sulphides and mineral weathering. Evaluating the relative contribution of these sources and processes to SO42? export is important to our understanding of S cycling as well as to policy makers in their evaluation of the efficacy of S emission controls. In order to evaluate the potential for mineral weathering contributions to SO42? export, we measured concentration and isotopic composition (δ34S and δ18O) of SO42? in stream water, and concentration and δ34S values of four S fractions in bedrock and soil parent material in catchments of varying geological composition. Geological substrates with low S concentrations were represented by catchments underlain by quartzite and granite, whereas geological substrates with high S concentrations were represented by catchments underlain by sulphidic slate, schist and metavolcanic rocks. Catchments with S‐poor bedrock had stream‐water SO42? concentrations <100 µeq L?1 and isotopic values consistent with those of atmospheric SO42? that had been cycled through the organic soil pool. Catchments with S‐rich bedrock had stream‐water SO42? concentrations ranging from 56 to 229 µeq L?1. Isotopic values deviated from those of SO42? in atmospheric deposition, clearly indicating a mineral weathering source in some cases, whereas in others spatial variability of mineral δ34S values precluded the isotopic detection of a weathering contribution. These results, along with evidence suggesting formation of secondary sulphate minerals in bedrock weathering rinds, indicate that mineral weathering may be an important source of S in the surface waters of some forested catchments in the northeastern USA. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

20.
Continental weathering plays a dominant role in regulating the global carbon cycle, soil chemistry and nutrient supply to oceans. The CO2-mediated silicate weathering acts as a major CO2 sink, whereas sulphuric acid-mediated carbonate dissolution releases CO2 to the atmosphere–ocean system. In this study, dissolved major ions and silica concentrations of two tropical (Damodar and Subarnarekha) river systems from India have been measured to constrain the type and rate of chemical weathering for these basins. The total dissolved solids (TDS) of these rivers, a measure of total solute supply from all possible sources, are about 2–3 times higher than that of the global average for rivers. Mass balance calculations involving inverse modelling estimate that 63 ± 11% of total cations are derived from rock weathering, of which 27 ± 7% of cations are supplied through silicate weathering. The sulphide-S concentrations are estimated by comparing the water chemistry of these two rivers with that of a nearby river (Brahmani) with similar lithology but no signatures of sulphide oxidation. The outflows of Damodar and Subarnarekha rivers receive 17% and 55% of SO4 through sulphide oxidation, respectively. The sulphide oxidation fluxes from the ore mining areas, such as upper Damodar (0.52 × 109 mol/yr) and lower Subarnarekha (0.66 × 109 mol/yr) basins, are disproportionally (~9 times) higher compared to their fractional areal coverage to the global drainage area. The corresponding CO2 release rate (2.84 × 104 mol/km2/yr) for the Damodar basin is lower by five times than its CO2 uptake rate (1.38 × 105 mol/km2/yr). The outcomes of this study underscore the dominance of sulphide oxidation in controlling the dissolved chemical (cationic and sulphur) fluxes.  相似文献   

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