Using Rock‐Eval 6 pyrolysis for tracking fossil organic carbon in modern environments: implications for the roles of erosion and weathering

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.     

Temporal variation of chemical and mechanical weathering in NE Iceland: Evaluation of a steady-state model of erosion

This study critically assesses the temporal sensitivity of the steady-state model of erosion that has been applied to chemical and mechanical weathering studies of volcanic islands and the continents, using only one sample from each catchment. The model assumes a geochemical mass balance between the initially unweathered rock of a drainage basin and the dissolved and solid loads of the river.Chemical composition of 178 samples of suspended and dissolved inorganic river constituents, collected in 1998–2002, were studied from five basaltic river catchments in NE Iceland. The Hydrological Service in Iceland has monitored the discharge and the total suspended inorganic matter concentration (SIM) of the glacial rivers for ~ four decades, making it possible to compare modelled and measured SIM fluxes.Concentration of SIM and grain size increased with discharge. As proportion of clay size particles in the SIM samples increased, concentrations of insoluble elements increased and of soluble decreased. The highest proportion of altered basaltic glass was in the clay size particles.The concentration ratio of insoluble elements in the SIM was used along with data on chemical composition of unweathered rocks (high-Mg basalts, tholeiites, rhyolites) to calculate the pristine composition of the original catchment rocks. The calculated rhyolite proportions compare nicely with area-weighted average proportions, from geological maps of these catchments.The calculated composition of the unweathered bedrock was used in the steady-state model, together with the chemical composition of the suspended and dissolved constituents of the river. Seasonal changes in dissolved constituent concentrations resulted in too low modelled concentrations of SIM_mod at high discharge (and too high SIM_mod at low discharge). Samples collected at annual average river dissolved load yielded SIM_mod concentrations close to the measured ones. According to the model, the studied rivers had specific mechanical denudation rates of 1.3–3.0 kg/m²/yr whereas the average measured rates were 0.8–3.5 kg/m²/yr which are among the highest on Earth.This study validates the use of a steady-state model of erosion to estimate mechanical weathering rates at the scale of a river catchment when the collected riverine dissolved load represents the average chemical composition over a mean hydrological year.     

Hydrological regulation of chemical weathering and dissolved inorganic carbon biogeochemical processes in a monsoonal river

To better understand the mechanisms relating to hydrological regulations of chemical weathering processes and dissolved inorganic carbon (DIC) behaviours, high-frequency sampling campaigns and associated analyses were conducted in the Yu River, South China. Hydrological variability modifies the biogeochemical processes of dissolved solutes, so major ions display different behaviours in response to discharge change. Most ions become diluted with increasing discharge because of the shortened reactive time between rock and water under high-flow conditions. Carbonate weathering is the main source of major ions, which shows strong chemostatic behaviour in response to changes in discharge. Ions from silicate weathering exhibit a significant dilution effect relative to the carbonate-sourced ions. Under high temperatures, the increased soil CO₂ influx from the mineralisation of organic material shifts the negative carbon isotope ratios of DIC (δ¹³C_DIC) during the high-flow season. The δ¹³C_DIC values show a higher sensitivity than DIC contents in response to various hydrological conditions. Results from a modified isotope-mixing model (IsoSource) demonstrate that biological carbon is a dominant source of DIC and plays an important role in temporal carbon dynamics. Furthermore, this study provides insights into chemical weathering processes and carbon dynamics, highlighting the significant influence of hydrological variability to aid understanding of the global carbon cycle.     

Dissolved organic carbon export from a cutover and restored peatland

High demand for horticultural peat has increased peatland drainage and peat extraction in Canada. The hydrology and carbon cycling of these cutover peatlands is greatly altered, necessitating active restoration efforts to permit the regeneration of Sphagnum mosses and the re‐establishment of natural peatland function. The effect of peatland extraction and restoration on the export of dissolved organic carbon (DOC) was examined for three successive seasons (May to October, 1999 to 2001) at two different sites (cutover and restored) in eastern Québec. A shift towards higher DOC concentrations was observed following peatland extraction (maximum: 182·6 mg L^?1) and concentrations remained high post‐restoration (maximum: 191·0 mg L^?1). The cutover site exported more DOC than the restored site in all three study seasons. The highest exports occurred during the wettest year (1999), with cutover and restored site export of 10·3 and 4·8 g m^?2, respectively. In 2000, 8·5 g C m^?2 was released from the cutover site, while the restored site released less than half that amount (3·4 g C m^?2). In 2001, the restored site released about the same amount of DOC as in the previous year (3·5 g C m^?2), while the cutover site load dropped to 6·2 g C m^?2. Both sites were net exporters of DOC in all years. Copyright © 2007 John Wiley & Sons, Ltd.     

Banking carbon: a review of organic carbon storage and physical factors influencing retention in floodplains and riparian ecosystems

Rivers are dynamic components of the terrestrial carbon cycle and provide important functions in ecosystem processes. Although rivers act as conveyers of carbon to the oceans, rivers also retain carbon within riparian ecosystems along floodplains, with potential for long‐term (> 10² years) storage. Research in ecosystem processing emphasizes the importance of organic carbon (OC) in river systems, and estimates of OC fluxes in terrestrial freshwater systems indicate that a significant portion of terrestrial carbon is stored within river networks. Studies have examined soil OC on floodplains, but research that examines the potential mechanistic controls on OC storage in riparian ecosystems and floodplains is more limited. We emphasize three primary OC reservoirs within fluvial systems: (1) standing riparian biomass; (2) dead biomass as large wood (LW) in the stream and on the floodplain; (3) OC on and beneath the floodplain surface, including litter, humus, and soil organic carbon (SOC). This review focuses on studies that have framed research questions and results in the context of OC retention, accumulation and storage within the three primary pools along riparian ecosystems. In this paper, we (i) discuss the various reservoirs for OC storage in riparian ecosystems, (ii) discuss physical conditions that facilitate carbon retention and storage in riparian ecosystems, (iii) provide a synthesis of published OC storage in riparian ecosystems, (iv) present a conceptual model of the conditions that favor OC storage in riparian ecosystems, (v) briefly discuss human impacts on OC storage in riparian ecosystems, and (vi) highlight current knowledge gaps. Copyright © 2015 John Wiley & Sons, Ltd.     

不同时间尺度青海湖沉积物总有机碳对气候变化的敏感性

湖泊沉积物总有机碳（TOC）含量通常作为表征流域和湖泊生产力的指标,在亚洲季风区也常常被当作夏季风的代用指标,被广泛应用于气候与环境变化研究.本文梳理了过去千年、全新世以及冰期-间冰期时间尺度上青海湖沉积物TOC的变化特征,并探讨了其指示气候变化的敏感性与有效性.结果表明,过去千年青海湖沉积物TOC含量与区域暖季温度和降水表现出较为一致的周期性波动.通过对比全新世区域夏季温度、基于孢粉的降水定量重建结果,以及湖泊水位、风沙活动反映的湿度状况等,发现不能简单地将青海湖沉积物TOC含量或沉积通量作为夏季风强度或者季风降水强度的代用指标.青海湖沉积物TOC含量在冰期和间冰期表现出巨大的差异,指示了冰期-间冰期时间尺度上较大的温度与降水变幅.因此,不同地域条件及不同时间尺度下,湖泊沉积物TOC对气候变化的敏感性不同,将湖泊沉积物TOC含量作为亚洲夏季风的代用指标需要特别谨慎,特别是在高寒气候区.     

Dissolved organic carbon transport in the Qilian mountainous areas of China

The Dissolved Organic Carbon (DOC) content of rivers is the most significant part of the carbon cycle migration in the basin under consideration, and it is the basis for a comprehensive understanding of the regional carbon cycle. In this study, we periodically collected samples from four monitoring stations in the Xiying River Basin of the Qilian Mountains in the northern Qinghai-Tibet Plateau. We calculated the fluxes of organic carbon in the rivers within the study area and have discussed the influencing factors of DOC concentration in these rivers. The results showed that: (a) The DOC concentration and transport flux of the Xiying river showed significant seasonal changes. The DOC concentration during summer and autumn was higher than that in winter and spring, and the output flux in summer and autumn accounted for approximately 88.3% of the total annual output. (b) Precipitation runoff has a higher DOC concentration than meltwater runoff. Climate factors, river-water chemical characteristics, and seasonal frozen-soil changes in the river basin have significant effects on the river DOC concentration and transport flux. (c) Larger runoff causes higher DOC concentrations in rivers. Runoff is the primary means of carbon migration in the inland river basin. Carbon migration is significant from the upstream to the middle and downstream sections of the inland river basin.     

Seasonal and spatial variation in suspended matter,organic carbon,nitrogen, and nutrient concentrations of the Senegal River in West Africa

The Senegal River is of intermediate size accommodating at present about 3.5 million inhabitants in its catchment. Its upstream tributaries flow through different climatic zones from the wet tropics in the source area in Guinea to the dry Sahel region at the border between Senegal and Mauritania. Total suspended matter, particulate and dissolved organic carbon and nitrogen as well as nutrient concentrations were determined during the dry and wet seasons at 19 locations from the up- to downstream river basin. The aims of the study were to evaluate the degree of human interference, to determine the dissolved and particulate river discharges into the coastal sea and to supply data to validate model results. Statistical analyses showed that samples from the wet and dry season are significantly different in composition and that the upstream tributaries differ mainly in their silicate and suspended matter contents. Nutrient concentrations are relatively low in the river basin, indicating low human impact. Increasing nitrate concentrations, however, show the growing agriculture in the irrigated downstream areas. Particulate organic matter is dominated by C4 plants during the wet season and by aquatic plankton during the dry season. The total suspended matter (TSM) discharge at the main gauging station Bakel was about 1.93 Tg yr⁻¹ which is in the range of the only available literature data from the 1980s. The calculated annual discharges of particulate organic carbon (POC), dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) are 55.8 Gg yr⁻¹, 54.1 Gg yr⁻¹, and 5.3 Gg yr⁻¹, respectively. These first estimates from the Senegal River need to be verified by further studies.     

Organic carbon fluxes of a glacier surface: A case study of Foxfonna,a small Arctic glacier

Arctic glaciers are rapidly responding to global warming by releasing organic carbon (OC) to downstream ecosystems. The glacier surface is arguably the most biologically active and biodiverse glacial habitat and therefore the site of important OC transformation and storage, although rates and magnitudes are poorly constrained. In this paper, we present measurements of OC fluxes associated with atmospheric deposition, ice melt, biological growth, fluvial transport and storage (in superimposed ice and cryoconite debris) for a supraglacial catchment on Foxfonna glacier, Svalbard (Norway), across two consecutive years. We found that in general atmospheric OC input (averaging 0.63 ± 0.25 Mg a^-1 total organic carbon, i.e. TOC, and 0.40 ± 0.22 Mg a^-1 dissolved organic carbon, i.e. DOC) exceeded fluvial OC export (0.46 ± 0.04 Mg a^-1 TOC and 0.36 ± 0.03 Mg a^-1 DOC). Early in the summer, OC was mobilised in snowmelt but its release was delayed by temporary storage in superimposed ice on the glacier surface. This delayed the export of 28.5% of the TOC in runoff. Biological production in cryoconite deposits was a negligible potential source of OC to runoff, while englacial ice melt was far more important on account of the glacier's negative ice mass balance (–0.89 and –0.42 m a^-1 in 2011 and 2012, respectively). However, construction of a detailed OC budget using these fluxes shows an excess of inputs over outputs, resulting in a net retention of OC on the glacier surface at a rate that would require c. 3 years to account for the OC stored as cryoconite debris. © 2018 John Wiley & Sons, Ltd.     

Towards constraining the magnitude of global agricultural sediment and soil organic carbon fluxes

Reliable quantitative data on the extent and rates of soil erosion are needed to understand the global significance of soil‐erosion induced carbon exchange and to underpin the development of science‐based mitigation strategies, but large uncertainties remain. Existing estimates of agricultural soil and soil organic carbon (SOC) erosion are very divergent and span two orders of magnitude. The main objective of this study was to test the assumptions underlying existing assessments and to reduce the uncertainty associated with global estimates of agricultural soil and SOC erosion. We parameterized a simplified erosion model driven by coarse global databases using an empirical database that covers the conterminous USA. The good agreement between our model results and empirical estimates indicate that the approach presented here captures the essence of agricultural erosion at the scales of continents and that it may be used to predict the significance of erosion for the global carbon cycle and its impact on soil functions. We obtained a global soil erosion rate of 10.5 Mg ha^‐1 y^‐1 for cropland and 1.7 Mg ha^‐1 y^‐1 for pastures. This corresponds to SOC erosion rates of 193 kg C ha^‐1 y^‐1 for cropland and 40.4 kg C ha^‐1 y^‐1 for eroding pastures and results in a global flux of 20.5 (±10.3) Pg y^‐1 of soil and 403.5 (±201.8) Tg C y^‐1. Although it is difficult to accurately assess the uncertainty associated with our estimates of global agricultural erosion, mainly due to the lack of model testing in (sub‐)tropical regions, our estimates are significantly lower than former assessments based on the extrapolation of plot experiments or global application of erosion models. Our approach has the potential to quantify the rate and spatial signature of the erosion‐induced disturbance at continental and global scales: by linking our model with a global soil profile database, we estimated soil profile modifications induced by agriculture. This showed that erosion‐induced changes in topsoil SOC content are significant at a global scale (an average SOC loss of 22% in 50 years) and agricultural soils should therefore be considered as dynamic systems that can change rapidly. Copyright © 2011 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.     

Export of fine particulate organic carbon from redwood‐dominated catchments

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.     

Response of soil aggregate disintegration to the different content of organic carbon and its fractions during splash erosion

Aggregate disintegration is a critical process in soil splash erosion. However, the effect of soil organic carbon (SOC) and its fractions on soil aggregates disintegration is still not clear. In this study, five soils with similar clay contents and different contents of SOC have been used. The effects of slaking and mechanical striking on splash erosion were distinguished by using deionized water and 95% ethanol as raindrops. The simulated rainfall experiments were carried out in four heights (0.5, 1.0, 1.5 and 2.0 m). The result indicated that the soil aggregate stability increased with the increases of SOC and light fraction organic carbon (LFOC). The relative slaking and the mechanical striking index increased with the decreases of SOC and LFOC. The reduction of macroaggregates in eroded soil gradually decreased with the increase of SOC and LFOC, especially in alcohol test. The amount of macroaggregates (>0.25 mm) in deionized water tests were significantly less than that in alcohol tests under the same rainfall heights. The contribution of slaking to splash erosion increased with the decrease of heavy fractions organic carbon. The contribution of mechanical striking was dominant when the rainfall kinetic energy increased to a range of threshold between 9 J m⁻² mm⁻¹ and 12 m⁻² mm⁻¹. This study could provide the scientific basis for deeply understanding the mechanism of soil aggregates disintegration and splash erosion.     

On the use of loss‐on‐ignition techniques to quantify fluvial particulate organic carbon

The fluvial flux of carbon (C) from terrestrial to marine environments represents an important component of the global C‐cycle, which can transfer C from the atmosphere to sedimentary storage. Fluvial fluxes of C are also an essential resource for freshwater ecosystems, critical for habitat heterogeneity and function. As such it is crucial that we are able to quantify this flux accurately. However, at present there are a number of different techniques used to quantify concentrations of fluvial C, and these techniques vary in their accuracy. In this article, we compare particulate organic carbon (POC) measurements derived from two commonly‐used techniques; a simple combustion and loss‐on‐ignition (LOI) technique, and an oxidative–combustion and carbon dioxide (CO₂) detection technique. The techniques were applied to water samples collected from 10 contrasting reference‐condition, temperate river ecosystems. The POC measurements derived from the LOI technique were up to 16 times higher (average four times higher), than those derived from the oxidative–combustion and CO₂ detection technique. This difference was highly variable both across the different river ecosystems and within each river ecosystem over time, suggesting that there is no simple way of converting the mass measured by LOI to estimates of fluvial POC. It is suggested that the difference in POC measured by these two techniques is a consequence of: (1) the loss of inorganic carbon at LOI combustion temperatures of > 425 °C, (2) the potential during the LOI combustion stage to lose hygroscopic and intercrystalline water, not completely driven off by the drying stage at temperatures of < 150 °C, and (3) the variable C content of fluvial organic matter, meaning that the simple application of a fixed correction factor to values obtained from the LOI technique may not be appropriate. These findings suggest that oxidative–combustion and CO₂ detection techniques are preferential for quantifying fluvial POC. Copyright © 2013 John Wiley & Sons, Ltd.     

Climate controls on coupled processes of chemical weathering,bioturbation, and sediment transport across hillslopes

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.     

过去5000 a以来抚仙湖沉积物有机质碳同位素的古环境指示意义

通过测定抚仙湖沉积物全有机样品的稳定碳同位素组成(δ~(13)C_(org))、总氮、总有机碳含量指标并计算碳氮比值,对过去5000 a以来抚仙湖沉积物有机质来源、δ~(13)C_(org)的影响因素及其所指示的古环境意义进行分析.结果表明:在过去的5000 cal a BP里,抚仙湖沉积物有机质主要来源发生明显变化,沉积物有机质输入由内源水生生物和陆生C_3植物共同输入(5000-2300 cal a BP阶段)转变为以内源沉水植物、浮游植物和藻类等输入为主(2000 cal a BP至今阶段);有机质来源发生变化是造成抚仙湖沉积物δ~(13)C_(org)值变化的主要原因;2000 cal a BP以来,陆源有机质输入的锐减与人类活动的影响密切相关;在2300-2000 cal a BP阶段,抚仙湖沉积物δ~(13)C_(org)值的快速变化可能指示了抚仙湖流域的古环境在这一时期经历了快速变化的气候事件.     

Riverine inputs of total organic carbon and suspended particulate matter from the Pearl River Delta to the coastal ocean off South China

A total of 1008 samples were collected from the eight major riverine runoff outlets in the Pearl River Delta (PRD) during 2005-2006 to estimate the fluxes of total organic carbon (TOC) to the coastal ocean off South China. The average dissolved organic carbon (DOC) concentration was 1.67 mg/L with a range of 1.38-2.13 mg/L. Concentrations of particulate organic carbon (POC) ranged from 2.66-4.12% of total suspended particulate matter (SPM). The fluxes of TOC and SPM from the PRD via the eight outlets were 9.2 x 10(5) and 2.5 x 10(7)tons/yr, respectively. Temporal variations in POC and DOC were observed at all outlets due to the large variability in runoff levels because of the seasonality of rainfall, and the riverine discharge amount was an important factor controlling TOC flux. The net contribution of organic carbon from the PRD to the coastal ocean represented approximately 0.1-0.2% of total organic carbon transported by rivers worldwide.     

富营养化湖泊沉积物有机质矿化过程中碳、氮、磷的迁移特征

采用室内培养的方法,以富营养化湖泊太湖为例,研究了沉积物有机质矿化过程中碳、氮、磷的迁移特征.结果表明,在沉积物中的有机质矿化过程中,碳以溶解性无机碳释放至水中,同时以CH4和CO2形式释放至大气中,培养结束时,CH4和CO2累积排放含量分别为1492.21和498.96 mg/g(dw),其中CH4占气态碳的89.16%(以C质量计);此外,大量的氮、磷营养盐释放至上覆水体,水中总氮、总磷和铵态氮的最高浓度分别是初始浓度的62.16、28.16和139.45倍,而硝态氮浓度在整个培养过程中逐渐下降,培养末期浓度是初期的0.21倍;厌氧条件下,沉积物有机质的矿化,不仅可以生成大量的CH4、CO2气体,还能够促使沉积物中铵态氮和磷的释放;而沉积物有机质矿化释放的碳、氮、磷营养元素又能加剧湖泊富营养化程度,促进湖泊水体的初级生产力,从而增加湖泊沉积物有机质输入.这样的循环方式可能是湖泊富营养化自维持的重要机制之一.     

Element geochemistry of weathering profile of dolomitite and its implications for the average chemical composition of the upper-continental crust

Geochemical behavior of chemical elements is studied in a dolomitite weathering profile in upland of karst terrain in northern Guizhou. Two stages can be recognized during the process ofin situ weathering of dolomitite: the stage of sedentary accumulation of leaching residue of dolomitite and the stage of chemical weathering evolution of sedentary soil. Ni, Cr, Mo, W and Ti are the least mobile elements with reference to Al. The geochemical behavior of REE is similar to that observed in weathering of other types of rocks. Fractionation of REE is noticed during weathering, and the two layers of REE enrichments are thought to result from downward movement of the weathering front in response to changes in the environment. It is considered that the chemistry of the upper part of the profile, which was more intensively weathered, is representative of the mobile components of the upper curst at the time the dolomitite was formed, while the less weathered lower profile is chemically representative of the immobile constitution. Like glacial till and loess, the “insoluble” materials in carbonate rocks originating from chemical sedimentation may also provide valuable information about the average chemical composition of the upper continental crust.     

Seasonal controls of meltwater runoff chemistry and chemical weathering at Urumqi Glacier No.1 in central Asia

Temporal variation of runoff chemistry and its seasonal controls relating to chemical weathering processes and drainage system evolution were examined at Urumqi Glacier No.1 in Xinjiang, China, over a full melt season. The dominant ions in meltwater runoff are HCO₃^?, Ca²⁺, and SO₄^2?; and Fe, Sr, and Al are dominant elements. Concentrations of major ions and some elements show periodic variations with seasons and negatively correlate with discharge, whereas other elements (e.g., Al, Ni, Cu, Zn, Cd, and Pb) show a random change, providing insights into the hydrological and physicochemical controls. HCO₃^? and Ca²⁺ are primarily derived from calcite, SO₄^2? and Fe mainly come from pyrite, and Sr and Al principally originate from silicate. Hydrochemical fluxes of solutes exhibit strong seasonality but are positively related to discharge, suggesting an increasing release of solutes during higher flow conditions. Solute yields, cation denudation rate, and chemical weathering intensity observed at Urumqi Glacier No.1 are higher than those at most basins worldwide. This suggests that chemical weathering in central Asia may be stronger than at other glacial basins with similar specific discharge. Concentrations of some elements (e.g., Fe, Al, As, Pb, and Zn) are close to or exceed the guidelines for drinking water standards in meltwater‐fed rivers. These rivers may face future challenges of water quality degradation, and relationships between changing flow and water quality conditions should be established soon, given that development of channelized flow is expected to be earlier over a melt season in a warming climate.