Rock chemical weathering by sulfuric acid: pathway,method and prospect

To investigate the role of sulfuric acid-based carbonate weathering in global CO_2 sequestration of climate changes, we systematically discussed the pathway of sulfuric acid in rock chemical weathering and its feedback mechanism for global warming. We showed the methods used to determine the accurate amount of sulfate flux,accounting for the sulfuric acid resulted from sulfide oxidation. Finally, we pointed out some prospects for further detailed work on the exact calculation of the sulfate fluxes for the CO_2 net-release.     

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.     

The O and H isotope characteristics of water from major rivers in China

Isotopic compositions of the water sources and evapotranspiration in large rivers of China are not well explored. In this investigation, d18 O and dD values of water from major large rivers of China are integrated to understand the spatial and temporal variations in the isotopes of water and d-excess. River water samples were collected from the channels and tributaries of the Changjiang, Yellow, Songhua and Liao Rivers in China. Water from upstream was generally enriched with light isotopes relative to that from downstream areas. Water from the Songhua River and upper reach of the Changjiang River has relatively negative isotopic values impacted by latitude and altitude effects, respectively. The spatial pattern showed that d18O-H2 O values in rivers mainly ranged from-9 to-7 % in most of China based on roughly mapped contours, and rivers enriched in light isotopes were primarily located in the Tibetan Plateau and northeast China The slopes of linear regression from the Yellow and Liao Rivers suggested that the loss of water by direct evaporation shifted the isotopes of water, especially in some small tributaries. Additionally, there was a narrow range of low d18OH2 O values from the main channel of rivers during the lowflow season relative to the high-flow season due to influence of the monsoon climate. No distinct spatial variation of d-excess values was found in the rivers of China. However, water samples in some rivers with low d-excess values had high d18 O values, indicating that evaporation in the tributaries has led to significant water loss, especially in tributaries of the Yellow and Liao Rivers.     

Organic carbon transport in the Songhua River,NE China: Influence of land use

Carbon transported by rivers is an important component of the global carbon cycle. Here, we report on organic carbon transport along the third largest river in China, the Songhua River, and its major tributaries. Water samples were collected seasonally or more frequently to determine dissolved organic carbon (DOC) and particulate organic carbon (POC) concentrations and C/N and stable carbon isotopic ratios. Principal component analysis and multiple regression analysis of these data, in combination with hydrological records for the past 50 years, were used to determine the major factors influencing the riverine carbon fluxes. Results indicate that the organic carbon in the Songhua River basin is derived mainly from terrestrial sources. In the 2008–2009 hydrological year, the mean concentrations of DOC and POC were 5.87 and 2.36 mg/L, and the estimated fluxes of the DOC and POC were 0.30 and 0.14 t·km^?2·year^?1, respectively. The riverine POC and DOC concentrations were higher in subcatchments with more cropland, but the area‐specific fluxes were lower, owing to decreased discharge. We found that hydrological characteristics and land‐use type (whether forest or cropland) were the most important factors influencing carbon transport in this system. Agricultural activity, particularly irrigation, is the principal cause of changes in water discharge and carbon export. Over the last 50 years, the conversion of forest to cropland has reduced riverine carbon exports mainly through an associated decrease in discharge following increased extraction of water for irrigation.     

Dissolved inorganic carbon isotopes of a typical alpine river on the Tibetan Plateau revealing carbon sources,wetland effect and river recharge

The Nyangqu River, the largest right bank tributary of the Yarlung Zangbo River in the Qinghai–Tibet Plateau, was representative of an alpine riverine carbon cycle experiencing climate change. In this study, dissolved inorganic carbon (DIC) spatial and seasonal variations, as well as their carbon isotopic compositions (δ¹³C_DIC) in river water and groundwater were systematically investigated to provide constraints on DIC sources, recharge and cycling. Significant changes in the δ¹³C_DIC values (from −2.9‰ to −23.4‰) of the water samples were considered to be the result of different contributions of two dominant DIC origins: soil CO₂ dissolution and carbonate weathering. Three types of rock weathering (dissolution of carbonate minerals by H₂CO₃ and H₂SO₄, and silicate dissolution by H₂CO₃) were found to control the DIC input into the riverine system. In DIC cycling, groundwater played a significant role in delivering DIC to the surface water, and DIC supply from tributaries to the main stream increased from the dry season to the wet season. Notably, the depleted δ¹³C_DIC ‘peak’ around the 88.9° longitude, especially in the September groundwater samples, indicated the presence of ‘special’ DIC, which was attributed to the oxidation of methane from the Jiangsa wetland located nearby. This wetland could provide large amounts of soil organic matter available for bacterial degradation, producing ¹³C-depleted methane. Our study provided insights regarding the role of wetlands in riverine carbon cycles and highlighted the contribution of groundwater to alpine riverine DIC cycles.     

Carbon biogeochemistry of ground water, Guiyang, southwest China

Variations in the concentrations and isotopic compositions (delta13C(DIC)) of dissolved inorganic carbon (DIC) reflect contamination and biogeochemical cycling of the carbon in ground water. In order to understand contamination and biogeochemical cycling of DIC, we carried out research on the geochemistry of ground water of Guiyang, the capital city of Guizhou Province, China. Results show that ground water is mainly characterized by SO4.HCO3-Ca.Mg and HCO3-Ca.Mg chemical compositions. The hydrochemical characteristics of these types of water are mainly controlled by lithology of the aquifers. HCO3- is the dominant species of DIC in ground water and has lower concentrations and more negative values of delta13C(DIC) in the high-flow (summer monsoon) season, as compared to the low-flow season. This indicates that DIC is relatively enriched in carbon of biological origin in the high-flow season as compared to the low-flow season and that biological activities are the predominant control on shifts of stable carbon isotope values. The evidence that the delta13C(DIC) values of ground water decrease with increasing concentrations of anthropogenic species shows that the carbon isotopic composition of DIC can be a useful tracer of contamination, in addition to biogeochemical cycling of inorganic carbon in ground water. Results from this study show that ground water is impacted by significant levels of contamination from human activities, especially in the urban areas, as well as the northeast and west suburbs, in Guiyang city, southwest China.     

Effects of hydrological processes on the chemical composition of riverine suspended sediment in the Zhujiang River,China

The chemical composition of riverine suspended sediment is the integration of the weathering crust minerals, soil organic matter and erosion agency within a specific drainage basin, which has been largely disturbed by the human activities. Selected metal elements of the riverine suspended sediment in the Zhujiang River were analysed using inductively coupled plasma–atomic emission spectrometry (ICP–AES) in three different hydrological phases from 1997 to 1998 at Makou and Sanshui hydrographic gauge stations, located at the lower reaches of the two main tributaries of the Zhujiang River, i.e. the Xijiang and the Beijing Rivers respectively. Organic carbon and nitrogen were also analysed using a conventional element analyser. The results demonstrate that the chemical composition of the riverine suspended sediment show obvious variability in different hydrological phases, which closely correlate to the organic matter content in suspended sediment. Intensified erosion in the flood phase results in lower concentration of the organic matter than that in the lower water level phase. The riverine suspended sediment with rich organic matter in the lower water level phase adsorbs some metal elements from the river water. Copyright © 2003 John Wiley & Sons, Ltd.     

Sr-Nd isotopic compositions of the Changjiang sediments: Implications for tracing sediment sources

The suspended particulate and fine-grained floodplain sediments were collected from the main stream and tributaries of the Changjiang River for Sr-Nd isotopic measurements. The εNd(0) values gradually decrease downstream from -10.8 on average in the upper reaches to -12.3 in the lower reaches, whereas the 87Sr/86Sr ratios increase correspondingly, averaging 0.721899 and 0.725826 respectively in the upper and middle-lower reaches. The compositional variations primarily reflect the complex con- trols of provenance rocks, chemical weathering, and sediment characters between different catchments, among which the abnormal Sr-Nd isotopic compositions of the Yalong, Fujiang, Tuojiang and Yuanjiang rivers indicate the sediment provenance contributions from the Emeishan Basalt in the upper reaches and the old metamorphic and siliceous rocks in the middle-lower reaches. The Sr-Nd isotopic ratios of the Changjiang sediments can better reflect the average composition of weathered continental crust compared to other major rivers in the world because of the unique source rock types in the Changjiang drainage basin. The recognition of the Sr-Nd isotopic systematics of the Changjiang sediments will contribute to our understanding of the Changjiang evolution history and continental weathering processes during the Cenozoic, and also to reconstructing the paleoenvironmental changes in East China and the marginal seas.     

Solute Sources and Processes in the Achankovil River Basin,Western Ghats,Southern India/Sources de Solutés et Processus Associés Dans le Bassin du Fleuve Achankovil,Ghats Occidentaux,Inde du Sud

Abstract

A time series survey was carried out in 2002 to understand the hydrogeochemical processes taking place in the Achankovil River of the Western Ghats Range. The water is neutral with pH and EC ranges from 6.32 to 7.56 and 24–54 µS cm^?1, respectively. Chloride and sodium are the dominant anion and cation in the water respectively. Correlation analysis of the chemical parameters of the water shows that few ions have additional sources. The majority of carbonate is derived from carbonate weathering followed by silicate weathering. Cation concentrations show decreasing trend from upstream to downstream in contrast to the increasing trend in the major world rivers. Dissolved silica in pre-monsoon water is low. The river chemistry is dominated by rock weathering induced by precipitation. Thermodynamic plots show that dolomite, kaolinite, albite and chlorite are in equilibrium with the river water. Chemical weathering is predominant here compared to physical weathering. The overall material transport seems to be lower compared to the other Indian rivers; nevertheless, the solute loads are comparable to certain large rivers such as the River Cauvery in southern India. The solute flux including the nutrient flux is very high among the Western Ghats rivers in relation to its size, which will certainly supplement the productivity of the lake/estuary and the coastal waters. Since this study is restricted to a one-year period, long-term data procurement and analysis along with micro nutrients studies are needed, which are lacking in the present study, to gain insight into the material flux by this river into the Arabian Sea.     

Spatial characteristics and controlling factors of chemical weathering of loess in the dry season in the middle Loess Plateau,China

Hydrochemistry methods were used to decipher the weathering and geochemical processes controlling solute acquisition of river waters in the dry season in the middle Loess Plateau (MLP), one of the most severely eroded areas and turbid riverine systems in the world. River waters were neutral to slightly alkaline with pH varying from 7.6 to 9.6. The total dissolved solids decreased from northwest to southeast with a mean value of 804 mg/l, much higher than the global average and other large rivers in China. Ternary diagram showed that river waters were dominated by Na⁺, HCO₃^?, and Cl^? with the main water‐type of HCO₃^?–Cl^?–Na⁺. Saturation index values, Mg²⁺, Ca²⁺, and HCO₃^? analyses indicated the preferential Ca²⁺ removal by calcite precipitation. Gibbs plots and stoichiometry plots indicated that the dissolved solutes were mainly derived from rock weathering with minor anthropogenic and atmospheric inputs. Samples in the northwestern basin are also influenced by evaporation. A forward model of mass budget calculation showed that, owing to high soluble characteristics, evaporite dissolution was a major feature of river waters and contributed 41% to the total dissolved cations on average, while carbonate and silicate weathering contributed 28%,and 25% on average, respectively. Besides evaporite dissolution, cation exchange is also responsible for the high concentrations of Na⁺ in river water. Spatial variations showed that evaporite dissolution and silicate weathering were higher in the northern basin, whereas carbonate weathering was higher in the southern basin. Different from most rivers in the world, the physical erosion rates (varying from 117.7 to 4116.6 t/km²y) are much higher than the chemical weathering rates (varying from 3.54 to 6.76 t/km²y) in the MLP because of the loose structure of loess and poor vegetation in the basin. In the future, studies on comparison of water geochemistry in different seasons and on influence of different types of land use and soil salinization on water geochemistry, denudation rates, and water quality should be strengthened in the MLP. These results shed some lights on processes responsible for modern loess weathering and also indicate the importance of time‐series sampling strategy for river water chemistry. Copyright © 2016 John Wiley & Sons, Ltd.     

河库连续体中溶解性无机碳及其同位素的时空分异特征——以澜沧江云南段为例

河流及水库等水生态系统中的溶解性无机碳(DIC)是全球碳循环与大气、陆地和海洋之间碳相互作用的重要组成部分.以澜沧江云南段上游天然河段及下游梯级水库群形成的连续体为研究对象,分析了河库连续体表层水体中水化学特征、溶解性无机碳浓度及其碳同位素时空分布特征.研究结果表明:河库连续体水体中溶解无机碳(DIC)及其同位素(δ13 C DIC)组成特征总体表现为:DIC浓度丰水期较低,枯水期较高,平均值分别为2.59±0.44和3.30±0.37 mmol/L;δ13 C DIC值丰水期偏负、枯水期偏正,平均值分别为-8.52‰±0.38‰和-6.95‰±0.53‰,与自然河流的季节变化特征相似.水体DIC来源主要包括土壤及水体有机质分解生成的CO 2、碳酸盐风化和水气界面CO 2的交换过程.澜沧江河库连续体中DIC浓度及δ13 C DIC组成的时空异质性特征与流域岩性、土壤生物地球化学过程以及微生物活动强度等均有较大关系.当前,澜沧江梯级水库群建库时间短,梯级联合运行下调度复杂,水文条件多变,梯级水库对河流重要生源要素——碳累积影响方面的“水库效应”还不明显.     

Isotopic signature of nitrate in river waters of the lower Mississippi and its distributary,the Atchafalaya

Periodic summer hypoxia occurring in the Northern Gulf of Mexico has been attributed to large nutrient inputs, especially nitrate‐nitrogen, from the Mississippi–Atchafalaya River system. The 2008 Gulf Hypoxia Action Plan calls for river corridor wetland restoration to reduce nitrate loads, but it is largely unknown how effective riverine wetland systems in the lower Mississippi River are for nitrate removal. We carried out an intensive isotope study to address this question by comparing nitrate isotopic signatures of the well‐channelized Mississippi River with those of the Atchafalaya River, which has extensive floodplains and backwater swamps. We investigated changes in δ¹⁵N_NO3 and δ¹⁸O_NO3 for water samples collected biweekly to monthly over a 2‐year period at the Atchafalaya River outlets (Morgan City and Wax Lake) and on the Mississippi River at Baton Rouge. In addition, in situ water quality parameters including temperature, dissolved oxygen and pH were recorded for each sampling date. Waters from both rivers showed moderately high nitrate concentration (>1 mg l^?1) and undetectable (< 0.01 mg l^?1) nitrite throughout the study period. The Mississippi River had slightly, but significantly higher (p=0.01) mean nitrate concentrations (1.5 mg l^?1) and higher δ¹⁵N_NO3 (7.7‰) than the Atchafalaya (1.1 mg l^?1, 7.0‰); while no difference in δ¹⁸O_NO3 (4.6‰) was found between the rivers. Flux‐weighted mean isotope values were overall lower than mean values for both the Mississippi and Atchafalaya Rivers, with a greater difference between the two rivers (7.4‰ versus 6.5‰, respectively). River flooding and hurricane storm surge also appeared to affect nitrate isotopic values. The lack of large difference in isotopic values between the Atchafalaya and Mississippi Rivers suggests that the majority of nitrate is transported through the Atchafalaya River with relatively little processing, and that riverine floodplains and wetlands are not effective sinks for nitrate, as previously assumed, because of insufficient residence time and well‐oxygenated river waters. Copyright © 2012 John Wiley & Sons, Ltd.     

Suspended sediment and dissolved load budgets of two Amazonian rivers from the Guiana Shield: Maroni River at Langa Tabiki and Oyapock River at Saut Maripa (French Guiana)

This study presents the data collected within the framework of an Observatory of Research in Environment on the Amazonian Basin—the ORE HYBAM. It relates to the dissolved and solid loads of the two main rivers of French Guiana, the Maroni and Oyapock rivers, running on the Guiana Shield and draining respectively 64 230 and 24 630 km². The low coefficient of variation of the average annual flows of the two rivers indicates an inter‐annual hydrological stability probably related to the immediate vicinity of the Atlantic Ocean. The sedimentary load is mainly composed of quartz and kaolinite. The total suspended solid (TSS) concentrations are among the world's lowest values; they range from 1 to 130 mg l⁻¹ during the hydrological cycle, with averages of 22 and 12 mg l⁻¹, for the Maroni and Oyapock rivers, respectively. The seasonal variability of these values is significantly higher than that of hydrologic flows, but without simple relationship with the discharge. Water chemical composition of the two rivers indicates a very weak mineralization, very similar to that found in the Amazonian rivers running on the Brazilian and Guianese shields, and in the Congo River and its tributaries in the Central African Shield. Seasonal variations are observed in both basins; they correspond to higher concentrations during low water stage (from October to February) and to more diluted water during the flood, from April to July. A signature enriched in Cl⁻ is present at the Saut Maripa station on the Oyapock River indicating a more marked influence of the trade winds in this basin. The computation of atmospheric contributions to ions budget indicated a weak contribution for Ca²⁺ and Mg²⁺, which originates mainly from water‐rock interactions in both stations, while more than half of Na⁺ is derived from atmospheric inputs. Copyright © 2010 John Wiley & Sons, Ltd.     

Source area and seasonal 87Sr/86Sr variations in rivers of the Amazon basin

We report the results of a detailed study of dissolved Sr isotopes in the Solimões and Beni‐Madeira Rivers of the Amazon basin. This study developed data collected over 8 years indicating large spatial and temporal variations in dissolved Sr isotopes among the rivers of the Amazon basin. The large ⁸⁷Sr/⁸⁶Sr variations were found to be correlated with the geology of the source areas of the suspended sediments. The Beni‐Madeira River displays a high average ⁸⁷Sr/⁸⁶Sr ratio and large ⁸⁷Sr/⁸⁶Sr fluctuations during the hydrological cycle. This large average value and fluctuations were related to the presence of Precambrian rocks and Ordovician sediments in the source area of the suspended sediment of the river. In contrast, the Solimões River displays a narrow range of Sr isotope ratio variations and an average value close to 0.709. This river drains mostly Phanerozoic rocks of northern Peru and Ecuador that are characterized by low Sr isotope ratios. The isotopic fluctuations in the Beni‐Madeira River were observed to propagate downstream at least as far as Óbidos. This signal is characterized by an inverse relationship between the concentration of elemental Sr and its isotopic ratios. We further demonstrate that the Sr isotopic composition and content in the Beni‐Madeira River is controlled by suspended sediments derived from the Andes. Despite draining areas underlain by Precambrian rocks and having high ⁸⁷Sr/⁸⁶Sr ratios, such rivers as the Negro and Tapajós play a minor role in the total Sr budget of the Amazon basin. Copyright © 2013 John Wiley & Sons, Ltd.     

The impact of the Three Gorges Dam on summer streamflow in the Yangtze River Basin

The Three Gorges Dam is the world's largest capacity hydropower station located in the Hubei province along the Yangtze River in China, which began operations in 2003. The dam also functions to store and regulate the downstream releases of water in order to provide flood control and navigational support in addition to hydropower generation. Flow regulation is particularly important for alleviating the impacts of low- and high-flow events during the summer rainy season (June, July, and August). The impact of dam operations on summer flows is the focus of this work. Naturalized flows are modelled using a canonical correlation analysis and covariates of subbasin-scale precipitation resulting in good model skill with an average correlation of 0.92. The model is then used to estimate natural flows in the period after dam operation. A comparison between modelled and gauged streamflow post 2003 is made and the impact of the dam on downstream flow is assessed. Streamflow variability is found to be strongly related to rainfall variability. An analysis of regional streamflow variability across the Yangtze River Basin showed a mode of spatially negatively correlated variability between the upper and lower basin areas. The Three Gorges Dam likely mitigated the occurrence of high-flow events at Yichang station located near the dam. However, the high flow at the remaining stations in the lower reach is not noticeably alleviated due to the diminishing influence of the dam on distant downstream flows and the impact of the lakes downstream of the dam that act to attenuate flows. Three types of flow regime changes between naturalized and observed flows were defined and used to assess the changes in the occurrence of high- and low-flow events resulting from dam operations.     

Alkalinity and dissolved inorganic carbon exports from tropical and subtropical river catchments discharging to the Great Barrier Reef,Australia

Dissolved inorganic carbon (DIC) transport by rivers is an important control on the pH and carbonate chemistry of the coastal ocean. Here, we combine DIC and total alkalinity (TAlk) concentrations from four tropical rivers of the Great Barrier Reef region in Australia with daily river discharge to quantify annual river loads and export rates. DIC in the four rivers ranged from 284 to 2,639 μmol kg⁻¹ and TAlk ranged from 220 to 2,612 μmol kg⁻¹. DIC:TAlk ratios were mostly greater than one suggesting elevated exports of free [CO₂*]. This was pronounced in the Johnstone and Herbert rivers of the tropical wet north. The largest annual loads were transported in the two large river catchments of the southern Great Barrier Reef region, the Fitzroy and Burdekin rivers. The carbon stable isotopic composition of DIC suggests that carbonate weathering was the dominant source of DIC in the southern rivers, and silicate weathering was likely a source of DIC in the northern Wet Tropics rivers. Annual loads and export rates were strongly driven by precipitation and discharge patterns, the occurrence of tropical cyclones, and associated flooding events, as well as distinct seasonal dry and wet periods. As such, short-lived hydrological events and long-term (seasonal and inter-annual) variation of DIC and TAlk that are pronounced in rivers of the tropical and subtropical wet and dry climate zone should be accounted for when assessing inorganic carbon loads to the coastal ocean and the potential to buffer against or accelerate ocean acidification.     

Weathering,Sr fluxes,and controls on water chemistry in the Lake Qinghai catchment,NE Tibetan Plateau

Strontium (Sr) concentrations and isotopic ratios have been measured in a series of water and rock samples from most of the major tributaries of the Lake Qinghai basin on the north‐eastern Tibetan Plateau. Dissolved Sr and ⁸⁷Sr/⁸⁶Sr show ranges of 488–12 240 nmol/l and 0·710497–0·716977, respectively. These data, together with measurements of major cations and anions in rivers and their tributaries and various lithologies of the catchment, were used to determine the contributions of Sr and its isotopic expense to rivers and lakes. Our results demonstrate that the chemical components and ⁸⁷Sr/⁸⁶Sr ratios of the alkaline waters are derived from mixing of carbonate and silicate sources, with the former contributing 72 ± 18% dissolved Sr to rivers. The difference in tributary compositions stems from the lithology of different river systems and low weathering intensity under a semi‐arid condition. Variation in ⁸⁷Sr/⁸⁶Sr ratios places constraint on the Sr‐isotopic compositions of the main tributaries surrounding Lake Qinghai. The water chemistry of the Buha River, the largest river within the catchment underlain by the late Paleozoic marine limestone and sandstones, dominates Sr isotopic composition of the lake water, being buffered by the waters from the other rivers and probably by groundwater. However, the characteristic chemical composition of the lake itself differs remarkably from the rivers, which can be attributed to precipitation of authigenic carbonates (low‐magnesium calcite, aragonite, and dolomite), though this does not impact the Sr isotope signature, which may remain a faithful indicator in paleo‐records. Regarding the potential role of groundwater input within the Lake Qinghai systems in the water budget and water chemistry, we have also determined the Sr concentration and ⁸⁷Sr/^S6Sr ratio of groundwater from diverse environments. This has allowed us to further constrain the Sr isotope systematic of this source. A steady‐state calculation gives an estimate for the groundwater flux of 0·19 ± 0·03 × 10⁸ m³/yr, accounting for about 8% of contemporary lake Sr budget. Copyright © 2010 John Wiley & Sons, Ltd.     

Sustaining environmental flows in water-deficient rivers via inter-basin hydropower transfer

In water-deficient rivers, environmental flows (e-flows) are usually sustained via inter-basin water transfer projects from water-sufficient rivers, but these projects incur tremendous costs and may lead to many negative ecological effects, such as ecological invasion. This research proposed to transfer hydropower instead of water from water-sufficient rivers, because hydropower could substitute for water to promote economic development and reduce water withdrawal from water-deficient rivers (conserved water). In addition, based on the analysis of eco-hydrological processes, the flow regime alteration plays an important role in restoring riverine ecosystem. With the goal of minimum flow regime alternation, we set up two scenarios to distribute the annual conserved water, and determined the optimal amount of transferred hydropower and the optimal use of conserved water, which could effectively sustain the e-flows. Accordingly, this paper established a computable general equilibrium model to analyse the substitution of hydropower for water in a water-deficient river basin, and determined the water withdrawal volume that could be reduced. We adopted a range-of-variability approach to measure the degree of flow regime alteration, and optimized the flow regime management scheme. The Luanhe River Basin was adopted as a study case. The results showed that: the water-hydropower equivalent decreased as the transferred hydropower into the Luanhe River Basin increased; a transferred hydropower amount of 22.46 kWh/s, equivalent to 18.30 m³/s conserved water, was optimal for the river basin; the conserved water should be distributed to the Luanhe River in the proportions of 0.55:0.1:0.35 during the wet, normal and dry seasons, respectively, which is the optimal scheme to sustain the hydrological processes of the river.     

Carbon dioxide,methane, and dissolved carbon dynamics in an urbanized river system

Estimates of greenhouse gas evasion from rivers have been refined over the past decades to constrain their role in global carbon cycle processes. However, despite 55% of the human population living in urban areas, urban rivers have had limited attention. We monitored carbon dynamics in an urbanized river (River Kelvin, 331 km², UK) to explore the drivers of dissolved carbon lateral and vertical export. Over a 2-year sampling period, riverine methane (CH₄) and carbon dioxide (CO₂) concentrations were consistently oversaturated with respect to atmospheric equilibria, leading to continual degassing to the atmosphere. Carbon stable isotopic compositions (δ¹³C) indicated that terrestrially derived carbon comprised most of the riverine CH₄ and dissolved CO₂ (CO₂*) load while dissolved inorganic carbon (DIC) from groundwater was the main form of riverine DIC. The dynamics of CH₄, CO₂*, and DIC in the river were primarily hydrology-controlled, that is, [CH₄] and [CO₂*] both increased with elevated discharge, total [DIC] decreased with elevated discharge while the proportion of biologically derived DIC increased with increasing discharge. The concentration of dissolved organic carbon (DOC) showed a weak relationship with river hydrology in summer and autumn and was likely influenced by the combined sewer overflows. Carbon emission to the atmosphere is estimated to be 3.10 ± 0.61 kg C·m⁻²·yr⁻¹ normalized to water surface area, with more than 99% emitted as CO₂. Annual carbon loss to the coastal estuary is approximately 4.69 ± 0.70 Gg C yr⁻¹, with annual DIC export approximately double that of DOC. Per unit area, the River Kelvin was a smaller carbon source to the atmosphere than natural rivers/streams but shows elevated fluxes of DIC and DOC under comparable conditions. This research illustrates the role urban systems may have on riverine carbon dynamics and demonstrates the potential tight link between urbanization and riverine carbon export.     

Temporal and spatial patterns of low-flow changes in the Yellow River in the last half century

Low-flow is widely regarded as the primary flow conditions for the anthropogenic and aquatic communities in most rivers, particularly in such an arid and semi-arid area as the Yellow River. This study presents a method integrating Mann–Kendall trend test, wavelet transform analysis and spatial mapping techniques to identify the temporal and spatial patterns of low-flow changes in the Yellow River (1955–2005). The results indicate that: (1) no trend can be identified in the major low-flow conditions in the upper Yellow River, but downward trends can be found in the middle and lower Yellow River; (2) similar periodic patterns are detected in the 7-day minima (AM7Q) in the upper and middle Yellow River, while different patterns are found in the lower Yellow River; (3) the increasing coefficients of variance in the primary low-flow conditions suggest that the variability of the low-flow is increasing from the upper to lower stream; (4) climate change and uneven temporal-spatial patterns of precipitation, jointly with highly intensified water resource utilization, are recognized as the major factors that led to the decrease of low-flow in the lower Yellow River in recent decades. The current investigation should be helpful for regional water resources management in the Yellow River basin, which is characterized by serious water shortage.