Carbon Isotopic Constrains on the Sources and Controls of the Terrestrial Carbon Transported in the Four Large Rivers in China

The Changjiang， Huanghe， Zhujiang and Heilongjiang are the four largest rivers in China and they transport large amount of fresh water and terrigenous materials， including both inorganic and organic carbon into the ocean. The sources of the terrestrial carbon transported in the four rivers， however， have not been well constrained and compared. In this study， we used carbon isotopes （¹³C and ¹⁴C） combined with concentration measurements to investigate and compare the sources and fluxes of Dissolved Inorganic Carbon （DIC）， Particulate Inorganic Carbon （PIC）， Dissolved Organic Carbon （DOC） and Particulate Organic Carbon （POC） in the four rivers. The contributions of the potential sources to both DIC and DOC were quantitatively calculated using a dual isotope and three end member model. The results showed that the concentrations and isotope characteristics of the carbon pools in the river depended largely on the geological setting， surrounding environment and the anthropogenic influence of the drainage basins. Compared with other large rivers in the world， the concentrations of DIC in the Changjiang， Huanghe and Zhujiang were higher， but the DIC fluxes in the Huanghe and Zhujiang were lower. The DOC concentrations in the Heilongjiang River were higher and lower in the other three rivers compared with the average value of the world largest 25 rivers. The Changjiang， Huanghe and Zhujiang all transport millennia aged carbon. The old riverine DIC reflects the influence of chemical weathering of carbonate rocks and the old DOC reflects influence mainly from pre-aged soil OC. These ancient terrestrial carbon discharged by the rivers could have significant effects on the carbon cycle and ecosystems in the China's marginal seas.     

Using Optical Properties to Quantify Fringe Mangrove Inputs to the Dissolved Organic Matter (DOM) Pool in a Subtropical Estuary

Dissolved organic carbon (DOC) concentration and dissolved organic matter (DOM) optical properties were analyzed along two estuarine river transects during the wet and dry seasons to better understand DOM dynamics and quantify mangrove inputs. A tidal study was performed to assess the impacts of tidal pumping on DOM transport. DOM in the estuaries showed non-conservative mixing indicative of mangrove-derived inputs. Similarly, fluorescence data suggest that some terrestrial humic-like components showed non-conservative behavior. An Everglades freshwater-derived fluorescent component, which is associated with soil inputs from the Northern Everglades, behaved conservatively. During the dry season, a protein-like component behaved conservatively until the mid-salinity range when non-conservative behavior due to degradation and/or loss was observed. The tidal study data suggests mangrove porewater inputs to the rivers following low tide. The differences in quantity of DOM exported by the Shark and Harney Rivers imply that geomorphology and tidal hydrology may be a dominant factor controlling the amount of DOM exported from the mangrove ecotone, where up to 21 % of the DOC is mangrove-derived. Additionally, nutrient concentrations and other temporal factors may control DOM export from the mangroves, particularly for the microbially derived fluorescent components, contributing to the seasonal differences. The wet and dry season fluxes of mangrove DOM from the Shark River is estimated as 0.27?×?10⁹ mg C d^?1 and 0.075?×?10⁹ mg C d^?1, respectively, and the Harney River is estimated as 1.9?×?10⁹ mg C d^?1 and 0.20?×?10⁹ mg C d^?1.     

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.     

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.     

Temporal variation and fluxes of dissolved and particulate organic carbon in the Apure,Caura and Orinoco rivers,Venezuela

The concentrations of total suspended sediments (TSS), dissolved organic carbon (DOC) and particulate organic carbon (POC) were measured in water samples taken monthly in the Apure, Caura and Orinoco rivers during a hydrological cycle (between Sept. 2007 and Aug. 2008). The DOC concentration values ranged between 1.5 and 6.8 mgC l⁻¹ in the Apure River; 2.07 and 4.9 mgC l⁻¹ in the Caura River and 1.66 and 5.35 mgC l⁻¹ in the Orinoco River. The mean concentration of DOC was 3.9 mgC l⁻¹ in the Apure River, 3.24 mgC l⁻¹ in the Caura River and 2.92 mgC l⁻¹ in the Orinoco River at Puerto Ordaz. The three rivers showed a similar temporal pattern in the concentrations of DOC, with higher DOC values during the increasing branch of the hydrograph due to wash-out processes of the organic material stored in soils. The mean concentration values of POC were 1.33 mgC l⁻¹; 0.77 mgC l⁻¹ and 0.91 mgC l⁻¹ in the Apure, Caura and Orinoco rivers, respectively. The inverse relationship found between the percentage in weight of the POC and the concentrations of TSS in the three rivers fits a logarithmic model, as it has been previously reported for other worldwide rivers. The POC concentrations in the Orinoco River showed a positive relationship with the TSS, suggesting that the POC in the Orinoco is the result of terrestrially organic matter. Although the fluxes of organic carbon (OC) in the three studied rivers are dependent on the values of water discharge, the fluxes of DOC during the increasing branch of the hydrograph are higher than those found during the decreasing stage, due to the yield of organic material accumulated in soils during the preceding dry season. The mean annual flux of total organic carbon (TOC) of the Orinoco River at Puerto Ordaz was about 4.27 × 10⁶ TonC yr⁻¹. Of this, 3.28 × 10⁶ TonC yr⁻¹ (77%) represents the flux of DOC and about 0.99 TonC yr⁻¹ (23%) represents the flux of POC. The mean annual input of TOC from the Apure River to the Orinoco River was about 4.92 × 10⁵ TonC yr⁻¹ (11.5%), while the contribution of TOC from the Caura River to the Orinoco River was estimated at 3.05 × 10⁵ TonC yr⁻¹ (7.1%).The values of annual transport of TOC calculated for the Apure, Caura and Orinoco rivers were lower than those reported twenty years ago. This could be related to interannual variations of precipitation in the Orinoco Basin, due to runoff variations can have a strong effect on the fluxes of OC from land to rivers.     

Assessment of carbonaceous aerosol over Delhi in the Indo-Gangetic Basin: characterization, sources and temporal variability

Semi-continuous measurements of organic carbon (OC) and elemental carbon (EC) and continuous measurements of black carbon (BC) and PM_2.5 aerosols were conducted simultaneously during the winter period of 2010–2011 at Delhi, one of the polluted urban megacities in western part of the Indo-Gangetic Basin region. The average mass concentrations of OC, EC, BC and PM_2.5 were about 54 ± 39, 10 ± 5, 12 ± 5 and 210 ± 146 μg m^?3, respectively. Contribution of total carbonaceous aerosol mass to PM_2.5 mass was found to be ~46 %. Average OC/EC ratio was found to be 5 ± 2 during the study period, suggesting the presence of secondary organic aerosols in the atmosphere over Delhi. Estimated mean secondary organic aerosol mass concentration was found to be 25 μg m^?3 and varied between 14.6 (February) and 37.0 μg m^?3 (December). A diurnal variation of OC and EC shows lower values during the day time and higher during the morning and night, which are highly associated with the corresponding variability in mixing layer heights. OC and EC were also found to be significantly correlated (r = 0.71) to each other, indicating their common sources. Concentrations of OC and EC were about 45 and 13 % higher during weekdays than weekends, respectively. Higher OC (67 %) and EC (53 %) were observed in the late evening during weekdays than those on weekends, which could be due to different emission sources during these two periods. The night/day ratio of EC and OC was found to be larger than 1.0, suggesting the relative accumulation of EC and OC near the surface at night hours.     

海洋溶解态黑碳的研究进展

溶解态黑碳(DBC)作为黑碳(BC)降解的中间产物,是海洋溶解有机碳碳库的重要组分,涉及全球海洋碳收支并进一步影响全球气候变化;是有色溶解有机质的重要组分,可改变水体光学环境从而对生态系统产生影响;也是一类良好的有机配体,在环境中易与金属离子形成络合物从而影响金属污染物的行为与毒性。鉴于其在气候变化、生态和环境等方面的重要影响,近年来研究者越来越关注DBC,并取得了一些基础性成果。目前,在DBC的定性认识上还存在一些模糊区域,所以DBC还没有一个明确的定义,DBC只是一个术语,特指一类由浓缩稠环母体和亲水性取代基(主要为羧基)组成的复杂有机物。在DBC的来源方面,已有证据证明BC降解能够产生DBC;但DBC很可能还存在其他来源,仍需进一步研究确认。DBC主要随水体进行迁移,并已观察到了DBC的降解现象,但目前对DBC的降解机理及速率仍不了解。在定量分析方法上,由于DBC的极性很强,且与其共存的基质相当复杂,分析DBC具有很大的挑战,其中苯多羧酸分子标志物法(BPCA)是定量分析DBC很有前景的方法之一,但目前仍存在一些难点需要解决。DBC在全球不同水体中含量变化很大,但目前的数据相当有限,不足以全面评估DBC的储量和循环周期。从DBC的定性识别、来源、迁移转化、定量分析及含量分布等方面综述DBC的研究进展,重点讨论BPCA法定量DBC的研究现状及存在问题,并展望DBC的研究方向。     

青藏高原东部长江流域盆地陆地化学风化研究

长江河水主要离子由流域盆地碳酸盐岩的风化所控制,沱沱河和楚玛尔河受蒸发盐岩影响较为明显;河水溶质载荷Si,Si/TZ *,Si/(Na* K)等指标表明,长江流域盆地地表硅酸盐岩风化还是浅表层次的;金沙江地表化学剥蚀速率为1.74×103mol/yr.km2,雅砻江为1.69×103mol/yr.km2,大渡河为1.57×103mol/yr.km2,岷江为1.88×103mol/yr.km2,长江河源区楚玛尔河为2.32×103mol/yr.km2,沱沱河为1.37×103mol/yr.km2,流域地表化学剥蚀速率可与世界上其它造山带的河流进行对比。     

Assessment of air quality during 19th Common Wealth Games at Delhi, India

The 19th Common Wealth Games was organized at Delhi, India, during October 3 to 14, 2010, where more than 8,000 athletes from 71 Commonwealth Nations have participated. In order to give them better environment information for proper preparedness, mass concentrations of particulate matters below 10 microns (PM₁₀) and 2.5 microns (PM_2.5), black carbon (BC) particles and gaseous pollutants such as carbon monoxide (CO) and nitrogen oxide (NO) were monitored and displayed online for ten different locations around Delhi, including inside and outside the stadiums. This extensive information system for air quality has been set up for the period from September 24 to October 21, 2010, and data have been archived at 5-min interval for further research. During the study period, average concentration of PM₁₀ and PM_2.5 was observed to be 229.7 ± 85.5 and 112.1 ± 56.0 μg m^?3, respectively, which is far in excess of the corresponding annual averages, stipulated by the national ambient air quality standards. Significant large and positive correlation (r = 0.93) between PM₁₀ and PM_2.5 implies that variations in PM₁₀ mass are governed by the variations in PM_2.5 mass. The mass concentrations of PM_2.5 inside the stadium were found to be ~18 % lower than those outside; however, no large variations were observed in PM₁₀. Mean concentrations of BC, CO and NO for the observation period were 10.9 μg m^?3 (Min, 02 μg m^?3; Max, 31 μg m^?3), 1.83 ± 0.89 ppm (Min, 0.48 ppm; Max, 4.55 ppm) and 37.82 ppb (Min, 2.4 ppb; Max, 206.05 ppb), respectively. BC showed positive correlation (r = 0.73) with CO suggests unified source for both of them, mainly from combustion emissions. All the measured parameters, however, show a significant diurnal variation with enhanced peaks in the morning and late night hours and lower values during daytime.     

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.     

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.     

Dissolved black nitrogen (DBN) in freshwater environments

Biomass burning results in the formation and accumulation of pyrogenic products such as black carbon (BC) and black nitrogen (BN) in soils. The ubiquitous presence of pyrogenic products in natural dissolved organic matter (DOM) and potential implications in global carbon cycling have recently been reported. However, little is known about the environmental dynamics or the importance in the global N cycle of dissolved BN (DBN; or heteroaromatic N). Here we report the coupling between DBN and dissolved BC (DBC) in ultrafiltered DOM from six headwater streams across a climatic region of North America, suggesting similar combustion sources, and that DOC may play an important role in the translocation of soil BN to the dissolved phase. The export of potentially recalcitrant riverine DBN to the ocean may affect the biogeochemical cycling of N and possibly the microbial community structure in aquatic environments.     

Seasonal and annual variations in the organic matter contributed by the St Lawrence River to the Gulf of St. Lawrence

The St. Lawrence River discharges a substantial volume of water (405 km³/a) containing suspended (SPM; 3.42 × 10⁶t) and dissolved (68.0 × 10⁶t) materials to the Gulf of St. Lawrence. The total load contains organic carbon in paniculate (POC; 3–14% of SPM), and dissolved (DOC; 3.76 ± 0.63 mg/l) form. The concentration of POC (and particulate organic nitrogen) is positively correlated with discharge (increased during the spring flood and the fall enhancement of flow), but concentration of DOC is not so simply related to discharge. In consequence, the total organic carbon (POC + DOC) load is relatively invariant, and increased annually by only 2–3% despite a progressive increase of 8% in discharge over the years of this study. Seasonal differences in the composition of the particulate organic matter (POM) are interpreted as reflecting dominant contributions from within-river production in summer and from terrestrial sources in spring and fall. In years when the annual discharge was greater than average, a higher proportion of the POM was terrigenous. The organic matter in surface sediments of the estuary to which the river discharges is predominantly of terrestrial provenance.     

Magnetic,geochemical and mineralogical properties of sediments from karstic and flysch rivers of Croatia and Slovenia

The aim of the present work was to investigate links between the low-field magnetic susceptibility (MS) and chemical and mineral composition of sediments from several Croatian and Slovenian rivers, as well as to determine possible anthropogenic influence on these sediments. MS measurements are a fast and simple method, which serves as a proxy for the estimation of pollution in different environmental systems. The investigated rivers are predominantly unpolluted rivers from Croatian and Slovenian karstic and flysch areas, which belong to the Adriatic or the Black Sea watersheds: the Dragonja, the Mirna, the Ra?a, the Ri?ana, the Reka, the Rak, the Cerkni?nica, the Unec and the Ljubljanica rivers. It was assumed that, due to their mostly unpolluted status, they could serve as a database for natural MS background values for this region. For comparison, several rivers and a lake from the Celje old metallurgic industrial area (Slovenia) were also investigated: the Savinja, the Hudinja, the Voglajna rivers and Slivni?ko Lake. They form a sub-basin of the Sava River drainage basin. Sediments of the clean karstic and flysch rivers showed extremely low MS values, with mass susceptibility values ranging from 0.58 × 10^?7 to 5.11 × 10^?7 m³/kg, and isothermal remanent magnetism (IRM) values ranging from 0.71 to 7.88 A/m. In the Celje industrial area, river sediments showed much higher MS values, with mass susceptibility values ranging from 1.31 × 10^?7 to 38.3 × 10^?7 m³/kg, and IRM values ranging from 0.91 to 100.42 A/m. The highest MS value was found in the Voglajna River at Teharje-?tore, a point which showed a significant number of anomalies of toxic metals in earlier investigations. Semiquantitative determination of relations between grain size and concentration of magnetite was performed using the Thompson-Oldfield method. X-ray diffraction (XRD) mineralogical analysis showed that sediments of the Celje area have mostly quartz as major mineral, with relatively small amount of carbonate minerals, while in sediments of karstic rivers carbonate minerals prevail. Statistically significant correlations were obtained between MS and Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd and Ba in the Slovenian karstic region and between MS and Cr, Fe, Co, Ni and Zn in flysch drainage basins. On the contrary, no correlation of MS and Hg content was obtained.     

Iron and Trace Metals in Microbial Mats and Underlying Sediments: Results From Guerrero Negro Saltern, Baja California Sur, Mexico

Total trace metals (Cd, Co, Cu, Fe, Mn, Ni, Pb, Zn), Al, and pyrite- and reactive-associated metals were measured for the first time in a microbial mat and its underlying anoxic-sulfidic sediment collected in the saltern of Guerrero Negro (GN), Baja California Sur, Mexico. It is postulated that the formation of acid volatile sulfide (AVS) and pyrite in the area of GN could be limited by the availability of reactive Fe, as suggested by its limited abundance (mat and sediment combined average value of only 19 ± 10 ??mol g^?1; n = 22) as well as the low pyrite (0.89?C7.9 ??mol g^?1) and AVS (0.19?C21 ??mol g^?1) concentrations (for anoxic-sulfidic sediments), intermediate degrees of pyritization (12?C50%), high degrees of sulfidization (14?C100%), generally low degrees of trace metal pyritization, and slight impoverishment in total Fe. This is a surprising result considering the large potential reservoir of available Fe in the surrounding desert. Our findings suggest that pyrite formation in the cycling of trace metals in the saltern of GN is not very important and that other sedimentary phases (e.g., organic matter, carbonates) may be more important reservoirs of trace elements. Enrichment factors [EF_Me = (Me/Al)_sample/(Me/Al)_background] of Co, Pb, and Cd were high in the mat (EF_Me = 2.2 ± 0.4, 2.8 ± 1.6 and 34.5 ± 9.8, respectively) and even higher in the underlying sediment (EF_Me = 4.7 ± 1.5, 14.5 ± 6.2 and 89 ± 27, respectively), but Fe was slightly impoverished (average EF_Fe of 0.49 ± 0.13 and 0.50 ± 0.27 in both mat and sediment). Organic carbon to pyrite-sulfur (C/S) molar ratios measured in the mat (2.9 × 10²?C27 × 10²) and sediment (0.81 × 10²?C6.6 × 10²) were, on average, approximately 77 times higher than those typically found in marine sediments (7.5 ± 2.1). These results may indicate that ancient evaporation basins or hypersaline sedimentary environments could be identified on the basis of extremely high C/S ratios (e.g., >100) and low reactive Fe.     

Sedimentation and Organic Carbon Burial in the Yangtze River and Hudson River Estuaries: Implications for the Global Carbon Budget

One of the most important challenges in global climate change research is balancing the carbon budget within the global carbon cycle. Carbon burial in sediments at the land–ocean interface has been difficult to quantify and model because it represents non-steady-state boundary conditions that are also affected by human activities. In this study, we document carbon burial rates in the Yangtze River (1.6–4.9 × 10¹² gC year^?1) and Hudson River (1.8–3.6 × 10¹⁰ gC year^?1) estuaries and integrate our results with carbon burial rates determined by others in the world’s 25 largest river-estuarine systems (6–11 × 10¹³ gC year^?1). Our results indicate that carbon burial in estuaries, bays, coves, lagoons, mud flats, marshes, mangroves, and other highly productive or protected low-energy areas at the land–ocean interface along the entirety of the world’s coastlines may serve as an unrecognized sink within the global carbon budget.     

Soil Organic Carbon Storage Changes in Coastal Wetlands of the Liaohe Delta,China, Based on Landscape Patterns

Growing wetland loss along a coastal area in China was examined through shoreline recession and land use changes. Carbon storage or sequestration in coastal wetland soils was based on vertical marsh accretion and aerial change data. Marshes sequester significant amounts of carbon through vertical accretion; however, large amounts of carbon previously sequestered in the soil profile are lost through rapid land use changes and shoreline recessions. The Liaohe Delta (LHD) was divided into nine landscape types based on Landsat TM digital images from 1991 to 2011. The distributed areas and transfer matrices of each landscape type were calculated. Combined with the organic carbon content and bulk density of 202 soil surface samples from field investigations in 2012, the soil organic carbon pools and stocks were estimated. Results showed that the soil organic carbon pools varied from 0.58 to 9.75 kg m^?2, and organic carbon storage in the upper 20 cm of soil was 1935.92 × 10⁴ and 1863.87 × 10⁴ t in 1991 and 2011, respectively. We attributed these large losses of carbon to rapid land use changes. The construction of levees along the shoreline has triggered large instantaneous losses of previously sequestered carbon through the destruction of 278.06 km² of tidal flats. Our results reveal that the LHD wetlands might not serve as a desired sink of carbon if maladministration practices are applied. These results can provide scientific guidance for decision makers in determining an effective way to maintain the soil carbon pool in the wetlands of the LHD.     

Methoxychlor bioremediation by defined consortium of environmental Streptomyces strains

Methoxychlor is an organochlorine pesticide used worldwide against several insect pests, resulting in human exposure. This pesticide mimics endocrine hormone functions, interfering with normal endocrine activity in humans and wildlife. For this reason, it is imperative to develop methods to remove this pesticide from the environment, and though, bioremediation using microorganisms results as an excellent strategy. Five Streptomyces spp. strains previously isolated from organochlorine-polluted sites and capable to grow and remove methoxychlor were combined as different mixed cultures to increase methoxychlor removal. From the 39 consortia tested, one consortium (Streptomyces spp. A6, A12, A14, M7) was selected because of its high pesticide removal and specific dechlorinase activity to be assayed on slurry and soil systems. This consortium showed higher biomass values (8.3 × 10⁶ ± 5.7 × 10⁵ CFU mL^?1) and methoxychlor removal (56.2 ± 2.3 %) on enriched slurry than in non-enriched slurry (7.3 × 10⁵ ± 1.2 × 10⁵ CFU mL^?1 and 45.6 ± 7.4 % of pesticide removal). In soil systems, Streptomyces consortium showed higher growth (1.0 × 10¹¹ ± 5.0 × 10¹⁰ CFU g^?1) than in enriched slurry, although differences in methoxychlor removal between both culture conditions were not statistically significant. Therefore, the selected Streptomyces consortium may be suitable for the development of in situ (soil) and ex situ (slurry bioreactor) bioremediation methods because of their potential to remove methoxychlor from different systems.     

Cadmium (II)-selective electrode based on palm shell activated carbon modified with task-specific ionic liquid: kinetics and analytical applications

In this study, palm shell activated carbon modified with task-specific ionic liquid was used as a novel electrode component for the potentiometric determination of cadmium ions in water samples. The proposed potentiometric sensor has good operating characteristics, including relatively high selectivity towards the Cd (II) ion, a Nernstian response to Cd (II) ions in a working concentration range of 1.0 × 10^?9–1.0 × 10^?2 M, with a reasonable detection limit of 1 × 10^?10 M and a slope of 30.90 ± 1.0 mV/decade. No significant changes in electrode potential were observed when the pH was varied over the range of 4–9. A direct technique based on the use of ion-selective electrode potentiometry has been developed in our laboratory for the study of reaction kinetics and kinetic methods of analysis by continuous monitoring of the rate of production or consumption of an ion. The apparent adsorption rate constant was estimated assuming pseudo-second-order kinetics. Additionally, the proposed electrode has been successfully used for the determination of the cadmium content in real samples without a significant interaction from other cationic or anionic species.     

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).