Freshwater-Saltwater Mixing Effects on Dissolved Carbon and CO<Subscript>2</Subscript> Outgassing of a Coastal River Entering the Northern Gulf of Mexico

The delivery of dissolved carbon from rivers to coastal oceans is an important component of the global carbon budget. From November 2013 to December 2014, we investigated freshwater-saltwater mixing effects on dissolved carbon concentrations and CO₂ outgassing at six locations along an 88-km-long estuarine river entering the Northern Gulf of Mexico with salinity increasing from 0.02 at site 1 to 29.50 at site 6 near the river’s mouth. We found that throughout the sampling period, all six sites exhibited CO₂ supersaturation with respect to the atmospheric CO₂ pressure during most of the sampling trips. The average CO₂ outgassing fluxes at site 1 through site 6 were 162, 177, 165, 218, 126, and 15 mol m^?2 year^?1, respectively, with a mean of 140 mol m^?2 year^?1 for the entire river reach. In the short freshwater river reach before a saltwater barrier, 0.079 × 10⁸ kg carbon was emitted to the atmosphere during the study year. In the freshwater-saltwater mixing zone with wide channels and river lakes, however, a much larger amount of carbon (3.04 × 10⁸ kg) was emitted to the atmosphere during the same period. For the entire study period, the river’s freshwater discharged 0.25 × 10⁹ mol dissolved inorganic carbon (DIC) and 1.77 × 10⁹ mol dissolved organic carbon (DOC) into the mixing zone. DIC concentration increased six times from freshwater (0.24 mM) to saltwater (1.64 mM), while DOC showed an opposing trend, but to a lesser degree (from 1.13 to 0.56 mM). These findings suggest strong effects of freshwater-saltwater mixing on dissolved carbon dynamics, which should be taken into account in carbon processing and budgeting in the world’s estuarine systems.     

Temporal Changes in Seawater Carbonate Chemistry and Carbon Export from a Southern California Estuary

Estuaries are important subcomponents of the coastal ocean, but knowledge about the temporal and spatial variability of their carbonate chemistry, as well as their contribution to coastal and global carbon fluxes, are limited. In the present study, we measured the temporal and spatial variability of biogeochemical parameters in a saltmarsh estuary in Southern California, the San Dieguito Lagoon (SDL). We also estimated the flux of dissolved inorganic carbon (DIC) and total organic carbon (TOC) to the adjacent coastal ocean over diel and seasonal timescales. The combined net flux of DIC and TOC (F_DIC?+?TOC) to the ocean during outgoing tides ranged from ??1.8±0.5?×?10³ to 9.5±0.7?×?10³?mol C h^?1 during baseline conditions. Based on these fluxes, a rough estimate of the net annual export of DIC and TOC totaled 10±4?×?10⁶?mol C year^?1. Following a major rain event (36 mm rain in 3 days), F_DIC?+?TOC increased and reached values as high as 29.0 ±?0.7?×?10³?mol C h^?1. Assuming a hypothetical scenario of three similar storm events in a year, our annual net flux estimate more than doubled to 25 ±?4?×?10⁶?mol C year^?1. These findings highlight the importance of assessing coastal carbon fluxes on different timescales and incorporating event scale variations in these assessments. Furthermore, for most of the observations elevated levels of total alkalinity (TA) and pH were observed at the estuary mouth relative to the coastal ocean. This suggests that SDL partly buffers against acidification of adjacent coastal surface waters, although the spatial extent of this buffering is likely small.     

Transport of terrestrial organic carbon to the oceans by rivers: re-estimating flux- and burial rates

 This study re-estimates one important component in the global carbon cycle: the modern global fluviatile organic carbon discharge- and burial rates. According to these results, approximately 430×10¹² g of terrestrial organic carbon are transported to the ocean in modern times. This amount is higher than the latest estimates but takes into account new data from Oceania not previously considered in global flux studies. However, only the minor amount of 10% or approximately 43×10¹² gC year^–1 is most likely buried in marine sediments. This amount is similar to the burial of marine organic carbon in the coastal ocean (55×10¹² gC year^–1). Adding both estimates gives approximately 100×10¹² gC year^–1, which is the value calculated by Berner (1982) for "terrestrial" deltaic-shelf sediments. However, the results in this study suggest that on a global scale the organic carbon content in coastal ocean sediments is not solely of terrestrial origin but a mixture of nearly equal amounts of marine and terrestrial organic carbon. The major part of the terrestrial organic carbon that enters the ocean by rivers (approximately 400×10¹² gC year^–1) seems to be either (a) remineralised in the ocean, whereas the mechanism by which the terrestrial organic carbon is oxidised in the ocean are unknown; or (b) is dispersed throughout the oceans and accumulates in pelagic sediments. Received: 9 November 1998 / Accepted: 25 May 1999     

Variability in Concentrations and Fluxes of Methane in the Indian Estuaries

In order to examine the fluxes of methane (CH₄) from the Indian estuaries, measurements were carried out by collecting samples from 26 estuaries along the Indian coast during high discharge (wet) and low water discharge (dry) periods. The CH₄ concentrations in the estuaries located along the west coast of India were significantly higher (113?±?40 nM) compared to the east coast of India (27?±?6 nM) during wet and dry periods (88?±?15 and 63?±?12 nM, respectively). Supersaturation of CH₄ was observed in the Indian estuaries during both periods ((0.18 to 22.3?×?10³ %). The concentrations of CH₄ showed inverse relation with salinity indicating that freshwater is a significant source. Spatial variations in CH₄ saturation were associated with the organic matter load suggesting that its decomposition may be another source in the Indian estuaries. Fluxes of CH₄ ranged from 0.01 to 298 μmol m^?2 day^?1 (mean 13.4?±?5 μmol m^?2 day^?1) which is ~30 times lower compared to European estuaries (414 μmol m^?2 day^?1). The annual emission from Indian estuaries, including Pulicat and Adyar, amounted to 0.39?×?10¹⁰ g CH₄?year^?1 with the surface area of 0.027?×?10⁶ km² which is significantly lower than that in European estuaries (2.7?±?6.8?×?10¹⁰ g CH₄?year^?1 with the surface area of 0.03?×?10⁶ km²). This study suggests that Indian estuaries are a weak source for atmospheric CH₄ than European estuaries and such low fluxes were attributed to low residence time of water and low decomposition of organic matter within the estuary. The CH₄ fluxes from the Indian estuaries are higher than those from Indian mangroves (0.01?×?10¹⁰ g CH₄?year^?1) but lower than those from Indian inland waters (210?×?10¹⁰ g CH₄?year^?1).     

Understanding the Cyclicity of Chemical Weathering and Associated CO<Subscript>2</Subscript> Consumption in the Brahmaputra River Basin (India): The Role of Major Rivers in Climate Change Mitigation Perspective

Weathering of rocks that regulate the water chemistry of the river has been used to evaluate the CO₂ consumption rate which exerts a strong influence on the global climate. The foremost objective of the present research is to estimate the chemical weathering rate (CWR) of the continental water in the entire stretch of Brahmaputra River from upstream to downstream and their associated CO₂ consumption rate. To establish the link between the rapid chemical weathering and thereby enhance CO₂ drawdown from the atmosphere, the major ion composition of the Brahmaputra River that drains the Himalaya has been obtained. Major ion chemistry of the Brahmaputra River was resolved on samples collected from nine locations in pre-monsoon, monsoon and post-monsoon seasons for two cycles: cycle I (2011–2012) and cycle II (2013–2014). The physico-chemical parameters of water samples were analysed by employing standard methods. The Brahmaputra River was characterized by alkalinity, high concentration of Ca²⁺ and HCO₃ ^? along with significant temporal variation in major ion composition. In general, it was found that water chemistry of the river was mainly controlled by rock weathering with minor contributions from atmospheric and anthropogenic sources. The effective CO₂ pressure (log\({{\text{P}}_{{\text{C}}{{\text{O}}_{\text{2}}}}}\)) for pre-monsoon, monsoon and post-monsoon has been estimated. The question of rates of chemical weathering (carbonate and silicate) was addressed by using TDS and run-off (mm year^?1). It has been found that the extent of CWR is directly dependent on the CO₂ consumption rate which may be further evaluated from the perspective of climate change mitigation The average annual CO₂ consumption rate of the Brahmaputra River due to silicate and carbonate weathering was found to be 0.52 (×10⁶ mol Km^?2 year^?1) and 0.55 (×10⁶ mol Km^?2 year^?1) for cycle I and 0.49 (×10⁶ mol Km^?2 year^?1) and 0.52 (×10⁶ mol Km^?2 year^?1) for cycle II, respectively, which were significantly higher than that of other Himalayan rivers. Estimation of CWR of the Brahmaputra River indicates that carbonate weathering largely dominates the water chemistry of the Brahmaputra River.     

Carbon dynamics of temperate grassland ecosystems in China from 1951 to 2007: an analysis with a process-based biogeochemistry model

Grasslands account for 40 % of the Chinese land area. About 80 % of the total grasslands are in the northern temperate zone. These grassland ecosystems provide goods and services to the local people and play an important role in the global carbon cycle. Remote sensing and ecosystem modeling approaches have been used to quantify the carbon budget of these grasslands. However, the intensive site measurements and meteorological data acquired in these ecosystems in the last few decades have not been adequately used to improve ecosystem model capabilities, in turn, better quantify their carbon budget. In this study an effort was made to examine the carbon budget and its spatial–temporal variation of the temperate grasslands in China from 1951 to 2007 using a process-based biogeochemistry model. It was found that the regional grasslands acted as a small carbon sink at 11.25 g C m^?2 year^?1 in the study area of 64.96 million hectares with a high inter-annual variability ranging from ?124 to 122.7 g C m^?2 year^?1 during the study period. As a result, the temperate grasslands sequestered about 410 Tg C in their vegetation and soils during the study period. The carbon sink occurred in typical steppe in central Inner Mongolia within the 300–400 mm rainfall zone and forest steppe in central and western China. By contrast, forest steppe in northeastern China mainly acted as a carbon source. Three major ecosystem types of forest steppe, typical steppe and desert steppe account for 54, 34, and 12 % of the total sink (7.3 Tg C year^?1) during 1951–2007, respectively. Soil moisture and evapotranspiration had a dominant effect on carbon budget in the typical steppe and the forest steppe while both water conditions and nitrogen mineralization rate were the major factors in the desert steppe. At a decadal scale, the air temperature significantly increased by 0.4 °C and annual precipitation insignificantly decreased by 0.2 mm; the regional carbon sink increased by 2.2 Tg C per decade during the period 1951–2007. However, further sensitivity analysis suggests that the sink of temperate grasslands will be reduced if the climate gets warmer and drier during this century since the increasing net primary production does not keep up with the increase of heterotrophic respiration.     

Isotope Constraints on the Aquatic Carbon Budget: Langat Watershed,Malaysia

Langat River drains a tropical watershed in the southwest of the Malaysian Peninsula. The watershed is heavily urbanized in its downstream portion. Water samples were collected from May 2010 to December 2011, at three localities along the main stem river, 1 location at its Semenyih tributary and from an upstream groundwater source. Concentration and δ¹³C data of riverine DIC and DOC indicate the dominance of C3 plant-derived material as the primary source of carbon, with δ¹³C_DIC values enriched in ¹³C relative to that of the C3 source. This enrichment is likely due to CO₂ outgassing, as calculated concentrations of riverine CO₂ are significantly higher than ambient atmospheric values, with methanogenic activity a theoretically possible contributing factor, particularly at the upstream location. The Langat River therefore acts as a net source of CO₂, with a total sub-basin flux of 19.7 × 10³ t C year^?1. This is comparable to the sum of riverine DOC, DIC and POC loss rates from the sub-basin, calculated as 24.5 × 10³ t C year^?1, and highlights the significance of CO₂ evasion from water bodies to the atmosphere for balancing the budget of the terrestrial carbon cycle. The DIC and DOC concentration and δ¹³C data also suggests that in the more urbanized downriver areas, much of the organic carbon input may be anthropogenicaly derived due to ubiquity of sewage treatment plants and landfill sites. Such human-induced perturbations to riverine carbon cycling should be taken into account in future studies of urbanized watersheds.     

An Evaluation of Temporal Changes in Sediment Accumulation and Impacts on Carbon Burial in Mobile Bay,Alabama, USA

The estuarine environment can serve as either a source or sink of carbon relative to the coastal ocean carbon budget. A variety of time-dependent processes such as sedimentation, carbon supply, and productivity dictate how estuarine systems operate, and Mobile Bay is a system that has experienced both natural and anthropogenic perturbations that influenced depositional processes and carbon cycling. Sediments from eight box cores provide a record of change in bulk sediment accumulation and carbon burial over the past 110 years. Accumulation rates in the central part of the basin (0.09 g cm^?2) were 60–80 % less than those observed at the head (0.361 g cm^?2) and mouth (0.564 g cm^?2) of the bay. Sediment accumulation in the central bay decreased during the past 90 years in response to both anthropogenic (causeway construction) and natural (tropical cyclones) perturbations. Sediment accumulation inevitably increased the residence time of organic carbon in the oxic zone, as observed in modeled remineralization rates, and reduced the overall carbon burial. Such observations highlight the critical balance among sediment accumulation, carbon remineralization, and carbon burial in dynamic coastal environments. Time-series analysis based solely on short-term observation would not capture the long-term effects of changes in sedimentation on carbon cycling. Identifying these relationships over longer timescales (multi-annual to decadal) will provide a far better evaluation of coastal ocean carbon budgets.     

Carbon Dioxide and Methane Emissions from Mangrove-Associated Waters of the Andaman Islands,Bay of Bengal

We estimated CO₂ and CH₄ emissions from mangrove-associated waters of the Andaman Islands by sampling hourly over 24 h in two tidal mangrove creeks (Wright Myo; Kalighat) and during transects in contiguous shallow inshore waters, immediately following the northeast monsoons (dry season) and during the peak of the southwest monsoons (wet season) of 2005 and 2006. Tidal height correlated positively with dissolved O₂ and negatively with pCO₂, CH₄, total alkalinity (TAlk) and dissolved inorganic carbon (DIC), and pCO₂ and CH₄ were always highly supersaturated (330–1,627 % CO₂; 339–26,930 % CH₄). These data are consistent with a tidal pumping response to hydrostatic pressure change. There were no seasonal trends in dissolved CH₄ but pCO₂ was around twice as high during the 2005 wet season than at other times, in both the tidal surveys and the inshore transects. Fourfold higher turbidity during the wet season is consistent with elevated net benthic and/or water column heterotrophy via enhanced organic matter inputs from adjacent mangrove forest and/or the flushing of CO₂-enriched soil waters, which may explain these CO₂ data. TAlk/DIC relationships in the tidally pumped waters were most consistent with a diagenetic origin of CO₂ primarily via sulphate reduction, with additional inputs via aerobic respiration. A decrease with salinity for pCO₂, CH₄, TAlk and DIC during the inshore transects reflected offshore transport of tidally pumped waters. Estimated mean tidal creek emissions were ～23–173 mmol m^?2 day^?1 CO₂ and ～0.11–0.47 mmol m^?2 day^?1 CH₄. The CO₂ emissions are typical of mangrove-associated waters globally, while the CH₄ emissions fall at the low end of the published range. Scaling to the creek open water area (2,700 km²) gave total annual creek water emissions ～3.6–9.2?×?10¹⁰ mol CO₂ and 3.7–34?×?10⁷ mol CH₄. We estimated emissions from contiguous inshore waters at ～1.5?×?10¹¹ mol CO₂?year^?1 and 2.6?×?10⁸ mol CH₄?year^?1, giving total emissions of ～1.9?×?10¹¹ mol CO₂?year^?1 and ～3.0?×?10⁸ mol CH₄?year^?1 from a total area of mangrove-influenced water of ～3?×?10⁴ km². Evaluating such emissions in a range of mangrove environments is important to resolving the greenhouse gas balance of mangrove ecosystems globally. Future such studies should be integral to wider quantitative process studies of the mangrove carbon balance.     

Role of Suspended Particulate Matter in Regulating the Behavior of Dissolved Uranium in the Yellow River Estuary

In order to examine the mixing behavior of dissolved uranium (U) in estuaries under different suspended particulate matter (SPM) regimes, three laboratory-based experiments were conducted by mixing seawater with river water containing different concentrations of SPM. Comparing this study with other field and laboratory-based experiments, dissolved U behaved differently depending upon the concentration of SPM. When SPM concentrations are >?0.8 g/L in the Yellow River, desorption/dissolution of U from SPM becomes predominant and dissolved U is enriched relative to the theoretical mixing line. However, when SPM concentrations are <?0.8 g/L, dissolved U behaves conservatively with some extent of removal during estuarine mixing. ²³⁴U/²³⁸U activity ratios were somewhat constant showing no measurable isotopic fractionation during physical mixing and U sorption/desorption to/from particles. Addition of dissolved ²³⁸U desorbed/dissolved from SPM during the annual Yellow River water-sediment regulation scheme (Jun 30th–Jul 14th, 2014) was estimated at 6.4?×?10¹¹ dpm, about 9% of the total riverine flux of dissolved ²³⁸U during that same period. This study represents a contribution to studies of dissolved U in muddy rivers and estuaries throughout the world. Results reported here provide not only a perspective to better estimate U flux from rivers to the ocean but also new insights into better understanding its estuarine mixing behavior and controlling factors.     

The streamflow trend in Tangwang River basin in northeast China and its difference response to climate and land use change in sub-basins

In this study, the hydro-climatic trends (1964–2006) of Tangwang River basin (TRB) were examined using the Kendall’s test. Moreover, the impacts of climate variability and land use change on streamflow in each sub-basin were assessed using the Soil and Water Assessment Tools (SWAT) model. The results indicated that annual mean flow and peak flow showed insignificant decreasing trends (?0.14 m³ s^?1 year^?1, 1 %; ?8.67 m³ s^?1 year^?1, 40 %), while annual low flow exhibited a slightly increasing trend (0.02 m³ s^?1 year^?1, 11 %). Correspondingly, the annual precipitation for the entire basin decreased by 0.02 mm year^?2, while the annual means of daily mean, maximum and minimum temperature increased significantly by 0.07, 0.10 and 0.02 °C year^?1, respectively. On the other hand, with the implementation of “Natural Forest Protection Project” and “Grain for Green Project”, the forests in TRB totally increased by 744.5 km² (4.00 %) from 1980 to 2000. Meanwhile, the grasslands and the farmlands decreased by 378.0 km² (?1.98 %) and 311.9 km² (?1.63 %), respectively. Overall, land use changes played a more important role for the streamflow reduction than climate change for SUB1, SUB2 and SUB3, in which the primary conversions were from grassland, farmland and bare land to forests. Conversely, in SUB4, the influence of climate variability was predominant. The results obtained could be a reference for water resources planning and management under changing environment.     

Carbon dioxide fluxes over a temperate meadow in eastern Inner Mongolia,China

Understanding the carbon dynamics in grassland is essential to precisely estimate global atmospheric carbon budget in response to climatic change. Eddy flux measurements were carried out during 2011 and 2012 to characterize seasonal and annual variability of carbon exchanges above a temperate meadow in eastern Inner Mongolia, China. The CO₂ flux showed obvious diurnal variations and the monthly mean amplitudes of diurnal course followed June/July > August > May > September. The daily maximum NEE reached up to ?8.0 and ?7.7 g C m^?2 for 2011 and 2012, respectively. CO₂ uptake was mainly from May to August, with seasonal peaks of ?16.0 g C m^?2 day^?1 in both two years. Gross primary production (GPP) and ecosystem respiration (Re) were ?1,084.5, 987.1 g C m^?2 year^?1 in 2011, and ?1,123.3, 1,040.2 g C m^?2 year^?1 in 2012, respectively. The meadow acted as a stable carbon sink, with integrated net ecosystem exchange (NEE) of ?97.4 and ?83.1 g C m^?2 year^?1 for 2011 and 2012, respectively. Compared with 2011, the ecosystem assimilated more carbon and meanwhile respired even more, leading to a less carbon sequestration in 2012. PAR and leaf area index (LAI) dominated the seasonal variations in NEE, with PAR explaining 61–69 % of the variance in NEE as LAI maintaining the plateau during June to July. Harvest significantly decreased ecosystem carbon uptake. The interannual variability in GPP and Re resulted primarily from the variations in temperature and its effect on biomass growth.     

Anaerobic Carbon Mineralisation Through Sulphate Reduction in the Inner Shelf Sediments of Eastern Arabian Sea

Monsoon-induced coastal upwelling, land run-off, benthic and atmospheric inputs make the western Indian shelf waters biologically productive that is expected to lead to high rates of mineralisation of organic matter (OM) in the sediments. Dissimilatory sulphate reduction (SR) is a major pathway of OM mineralisation in near-shore marine sediments owing to depletion of other energetically more profitable electron acceptors (O₂, NO₃ ^?, Mn and Fe oxides) within few millimetres of the sediment-water interface. We carried out first ever study to quantify SR rates in the inner shelf sediments off Goa (central west coast of India) using the ³⁵S radiotracer technique. The highest rates were recorded in the upper 10 cm of the sediment cores and decreased gradually thereafter below detection. Despite significant SR activity in the upper ～12 to 21 cm at most of the sites, pore water sulphate concentrations generally did not show much variation with depth. The depth integrated SR rate (0.066–0.46 mol m^?2 year^?1) decreased with increasing water depth. Free sulphide was present in low concentrations (0–3 μM) in pore waters at shallow stations (depth <30 m). However, high build-up of sulphide (100–600 μM) in pore waters was observed at two deeper stations (depths 39 and 48 m), 7–11 cm below the sediment-water interface. The total iron content of the sediment decreased from ～7 to 5 % from the shallowest to the deepest station. The high pyrite content indicates that the shelf sediments act as a sink for sulphide accounting for the low free sulphide levels in pore water. In the moderately organic rich (2–3.5 %) sediments off Goa, the measured SR rates are much lower than those reported from other upwelling areas, especially off Namibia and Peru. The amount of organic carbon remineralised via sulphate reduction was ～0.52 mol m^?2 year^?1. With an estimated average organic carbon accumulation rate of ～5.6 (±0.5) mol m^?2 year^?1, it appears that the bulk of organic matter gets preserved in sediments in the study region.     

Increased Terrestrial to Ocean Sediment and Carbon Fluxes in the Northern Chesapeake Bay Associated With Twentieth Century Land Alteration

We calculated Chesapeake Bay (CB) sediment and carbon fluxes before and after major anthropogenic land clearance using robust monitoring, modeling and sedimentary data. Four distinct fluxes in the estuarine system were considered including (1) the flux of eroded material from the watershed to streams, (2) the flux of suspended sediment at river fall lines, (3) the burial flux in tributary sediments, and (4) the burial flux in main CB sediments. The sedimentary maximum in Ambrosia (ragweed) pollen marked peak land clearance (~1900 a.d.). Rivers feeding CB had a total organic carbon (TOC)/total suspended solids of 0.24?±?0.12, and we used this observation to calculate TOC fluxes from sediment fluxes. Sediment and carbon fluxes increased by 138–269% across all four regions after land clearance. Our results demonstrate that sediment delivery to CB is subject to significant lags and that excess post-land clearance sediment loads have not reached the ocean. Post-land clearance increases in erosional flux from watersheds, and burial in estuaries are important processes that must be considered to calculate accurate global sediment and carbon budgets.     

Groundwater budget for the upper and middle parts of the River Gash Basin, eastern Sudan

The River Gash Basin is filled by the Quaternary alluvial deposits, unconformably overlying the basement rocks. The alluvial deposits are composed mainly of unconsolidated layers of gravel, sand, silt, and clays. The aquifer is unconfined and is laterally bounded by the impermeable Neogene clays. The methods used in this study include the carry out of pumping tests and the analysis of well inventory data in addition to the river discharge rates and other meteorological data. The average annual discharge of the River Gash is estimated to be 1,056?×?10⁶ m³ at El Gera gage station (upstream) and 587?×?10⁶ m³ at Salam-Alikum gage station (downstream). The annual loss mounts up to 40% of the total discharge. The water loss is attributed to infiltration and evapotranspiration. The present study proofs that the hydraulic conductivity ranges from 36 to 105 m/day, whereas the transmissivity ranges from 328 to 1,677 m²/day. The monitoring of groundwater level measurements indicates that the water table rises during the rainy season by 9 m in the upstream and 6 m in the midstream areas. The storage capacity of the upper and middle parts of the River Gash Basin is calculated as 502?×?10⁶ m³. The groundwater input reach 386.11?×?10⁶ m³/year, while the groundwater output is calculated as 365.98?×?10⁶ m³/year. The estimated difference between the input and output water quantities in the upper and middle parts of the River Gash Basin demonstrates a positive groundwater budget by about 20?×?10⁶ m³/year     

Conservative behaviour of riverine dissolved organic carbon in the Severn Estuary: chemical and geochemical implications

The distribution, variability and chemical behaviour of dissolved organic carbon (DOC) was investigated over 2$\text{1}\text{2}$ years in the Severn Estuary and Bristol Channel, UK. The concentrations of riverine DOC (3.1–7.8 mg C l^?1) covaried with river flow and were invariably conservative in this turbid slowly flushing (~200 days) estuary, indicating that any microbial degradation, chemical flocculation or adsorption processes do not affect the flux of riverine DOC through the estuary. The DOC inputs from the Severn (1.7–2.7 × 10¹⁰ g Cyr^?1) and other rivers (2.6–3.4 × 10¹⁰ g Cyr^?1) are the principal sources of DOC in the estuary and correspond to an export of 0.7–1.1% of the terrestrial productivity from the river catchment to the ocean. This export rate is in accord with recent predictions derived from global compilations of organic inputs from rivers and would imply that the global flux of riverine DOC could be as high as 7.8 × 10¹⁴ g Cyr^?1 which is 5 times greater than some previous estimates.The geochemical significance of a conservative delivery of riverine DOC to the ocean is that irrespective of which flux estimate is considered, such river inputs would make a significant contribution (~SO%) to oceanic DOC, and that the steady-state oceanic DOC flux would have to be significantly greater than present estimates (2.9 × 10¹⁴ g Cyr^?1) which are based on a mean radio carbon age of 3400 yr.An alternative, more realistic DOC flux model, which assumes a polydisperse age distribution about the mean age, is shown to yield the higher oceanic DOC fluxes required. Flocculation and adsorption processes would remove less than 10% and 0.2% respectively of riverine DOC in estuaries.     

Groundwater Discharge as a Source of Dissolved Carbon and Greenhouse Gases in a Subtropical Estuary

Groundwater may be highly enriched in dissolved carbon species, but its role as a source of carbon to coastal waters is still poorly constrained. Exports of deep and shallow groundwater-derived dissolved carbon species from a small subtropical estuary (Korogoro Creek, Australia, latitude ?31.0478°, longitude 153.0649°) were quantified using a radium isotope mass balance model (²³³Ra and ²²⁴Ra, natural groundwater tracers) under two hydrological conditions. In addition, air-water exchange of carbon dioxide and methane in the estuary was estimated. The highest carbon inputs to the estuary were from deep fresh groundwater in the wet season. Most of the dissolved carbon delivered by groundwater and exported from the estuary to the coastal ocean was in the form of dissolved inorganic carbon (DIC; 687 mmol m^?2 estuary day^?1; 20 mmol m^?2 catchment day^?1, respectively), with a large export of alkalinity (23 mmol m^?2 catchment day^?1). Average water to air flux of CO₂ (869 mmol m^?2 day^?1) and CH₄ (26 mmol m^?2 day^?1) were 5- and 43-fold higher, respectively, than the average global evasion in estuaries due to the large input of CO₂- and CH₄-enriched groundwater. The groundwater discharge contribution to carbon exports from the estuary for DIC, dissolved organic carbon (DOC), alkalinity, CO₂, and CH₄ was 22, 41, 3, 75, and 100 %, respectively. The results show that CO₂ and CH₄ evasion rates from small subtropical estuaries surrounded by wetlands can be extremely high and that groundwater discharge had a major role in carbon export and evasion from the estuary and therefore should be accounted for in coastal carbon budgets.     

Effects of glacier melting on socioeconomic development in the Manas River basin, China

This study used 46 years of recent data, including glacial area, temperature, precipitation, and runoff data, to examine the glacier melting and its possible socioeconomic effects in the Manas River basin in western China. The average yearly change in the glaciated area in the Manas River basin for the entire study period was 0.41 %, and the glacier mass balance mainly keeps negative in the last 46 years. The negative glacial mass balance observed between 1986 and 2006 was 2.8 times greater than that for the period 1960–1985. Additionally, the amount of meltwater runoff was 78 % greater in 1986–2006 than in 1960–1985, with a mean depth of 478 mm year^?1.Glacier melting and runoff in the Manas River basin during the late twentieth century were higher than at present. Annual meltwater volumes can reach 1 × 10⁸ m³, providing beneficial water resources to downstream areas. However, as the climate becomes warmer, the risk of meltwater flooding will also increase. Our calculations indicate that after the 2030s, the level of flooding risk will increase substantially.     

Quantities and Fluxes of Dissolved and Particulate Black Carbon in the Changjiang and Huanghe Rivers,China

Recent studies have suggested that large rivers play important roles in mobilizing and transporting black carbon (BC) from land to the ocean. However, the influence of the Changjiang and Huanghe, the two largest rivers in China, on the fate of BC has not been determined. In this paper, we present measurements of BC in both the dissolved and particulate phases in the Changjiang and Huanghe Rivers and in the coastal waters of the East China Sea (ECS). Our results show that dissolved black carbon (DBC) accounted for 3.0 ± 0.4 % and 4.8 ± 3.6 % of the total DOC pool in the Changjiang and Huanghe Rivers and 3.4 ± 0.6 % of the DOC pool in the coast of the ECS. In addition, particulate black carbon (PBC) accounted for 13 ± 0.9 % and 22 ± 11 % of the POC pool in the Changjiang and Huanghe Rivers, respectively. We calculate that the Changjiang and Huanghe transported 4.7 × 10¹⁰ gC and 1.7 × 10⁹ gC of DBC, and 2.0 × 10¹¹ gC and 1.2 × 10¹⁰ gC of PBC to the ECS and Bohai Sea in 2015. The large amounts of BC transported by the two rivers represent a major sink of anthropogenically derived organic carbon and could have a significant impact on the ecosystem and carbon cycling in China’s marginal seas.     

GIS-based lake sediment budget estimation taking into consideration land use change in an urbanizing catchment area

The objective of this study was to assess the lake sediment budget of land use changes using the Universal Soil Loss Equation (USLE), sediment delivery ratio (SDR), and trap efficiency (TE). The geographic information system was combined with the USLE to estimate the soil erosion of the Lake Asan watershed. Spatial data for each of the USLE factors were obtained from the land use, soil, and 1/25,000 scale digital contour maps. Landsat-5 TM images were selected for analyzing soil erosion changes due to land use changes. The sediment yield to Lake Asan was estimated using the SDR and TE. The estimated sediment budget was compared with observed data from the Lake Asan watershed between 1974 and 2003. The total estimated annual mean sediment budgets from Lake Asan in 1986, 1992, and 2000 were 0.267, 0.301, and 0.339 × 10⁶ ton, respectively, with an average of 0.302 × 10⁶ ton. The average measured sediment budget was 3.15 × 10⁶ ton year^?1. The average estimated value shows reasonable agreement with the observed sediment balance. The average estimated and measured sediment budgets contain uncertainties due to both the methods and the approach used by the observers. The simulated results indicated that soil erosion in the Lake Asan watershed increased at a rate of approximately 2 % per year from 1986 to 2000 due to land use change. This study may be useful for managers to identify reservoir rehabilitation management methods for stable irrigation water supply.