Stable isotopic composition of riverine dissolved inorganic carbon of the Xijiang River Inner Estuary

For researching the spatio-temporal variation of the stable isotopic composition of the riverine dissolved inorganic carbon（DIC）,we had carried out a survey throughout the hydrologic year during which theδ^13CDIC of the surface water and its physicochemical parameter were examined along the Xijiang River Inner Estuarine waterway from September 2006 to June 2007.There was a striking seasonal variation on the averageδ^13CDIC,as the averageδ^13CDIC in summer（-13.91‰）or autumn（-13.09‰）was much less than those in spring（-11.71‰）or winter（-12.26‰）.The riverineδ13C DIC was controlled by decomposed condition of the riverine organic matter linking the seasonal variation of the physicochemical parameter in the surface water according to the correlation analysis which indicated notable relations betweenδ^13CDIC and water temperature（p=0.000;r=-0.569）or betweenδ^13CDIC and oxide-reduction potential（p=0.000;r=0.646）.The striking positive correlation between δ^13CDIC and the sampling distance happened in the summer rainy season,while striking negative correlation happened in the spring dry season,indicating that river-sea interaction influenced water physicochemical parameters and controlled the riverine DIC property in the survey waterway.In view of the riverineδ^13CDIC decreasing for the decomposition of the terrestrial organic matter in the rainy season in summer and increasing for the briny invaded zone extending in the spring dry season along the waterway from the Makou gauging station to the Modaomen outlet,theδ^13CDIC spatio-temporal variation was closely related to the geographical environment of the Xijiang drainage basin.

Damming effects on dissolved inorganic carbon in different kinds of reservoirs in Jialing River,Southwest China

To assess the effects of river damming on dissolved inorganic carbon in the Jialing River, a total of 40 water samples, including inflow, outflow, and stratified water in four cascade reservoirs(Tingzikou, Xinzheng,Dongxiguan, Caojie) were collected in January and July,2016. The major cations, anions, and δ^(13)C_(DIC) values were analyzed. It was found that the dissolved compositions are dominated by carbonate weathering, while sulfuric acids may play a relatively important role during carbonate weathering and increasing DIC concentration. Different reservoirs had variable characteristics of water physiochemical stratification. The DIC concentrations of reservoir water were lower in summer than those in winter due to the dilute effects and intensive aquatic photosynthesis, as well as imported tributaries. The δ^(13)C_(DIC) values in Tingzikou Reservoir were higher during summer than those in winter,which indicated that intensive photosynthesis increased the δ^(13)C_(DIC) values in residual water, but a similar trend was not obvious in other reservoirs. Except for in Xinzheng Reservoir, the δ^(13)C_(DIC) values in inflow and outflow reservoir water were lower than those in the surface water of stratified sampling in summer. For stratified sampling, it could be found that, in summer, the Tingzikou Reservoir δ^(13)C_(DIC) values significantly decreased with water depthdue to the anaerobic breakdown of organic matter. The significant correlation(p<0.01 or 0.05) between the DIC concentrations, the δ^(13)C_(DIC) values and anthropogenic species(Na^++K^+, Cl~–, SO_4^(2-) and NO_3^-) showed that the isotope composition of DIC can be a useful tracer of contaminants. In total, Tingzikou Reservoir showed lacustrine features, Xinzheng Reservoir and Dongxiguan Reservoir had "transitional'' features, and Caojie Reservoir had a total of "fluvial'' features. Generally, cascade reservoirs in the Jialing River exhibited natural river features rather than typical lake features due to characteristics of reservoir water in physiochemical stratification, spatiotemporal variations of DIC concentrations and isotopic compositions. It is evident that the dissolved inorganic carbon dynamics of natural rivers had been partly remolded by dam building.

Photochemical production of dissolved inorganic carbon from suwannee river humic acid

The photochemical mineralization of dissolved organic carbon(DOC) to dissolved inorganic carbon(DIC) is a key process in carbon cycling.Using a Suntest CPS solar simulator,Suwannee River humic acid(SRHA) was photooxidated to examine the effects of O2 levels,the wavelength of incident light,and the concentration of Fe on the photoproduction of DIC.Increasing the O2 abundance enhanced photodegradation of SRHA.The rate of DIC photoproduction under air saturation in the first 24 h(4.40 μmol/(L h)) was increased by a factor of 1.56 under O2 saturation,but fell by only 36% under N2 saturation.To evaluate the relative importance of UV-B,UV-A,and visible radiation in the photodegradation,we examined the above process using Mylar-d films and UF-3 and UF-4 plexiglass filters.The results indicated that the UV-B,UV-A and visible wavelengths accounted for 31.8%,32.6% and 25.6%,respectively,of DIC production with simulated sunlight irradiation.The above results also indicated that photoproduction of DIC could take place in natural water at depths greater than those that UV light can reach.When 20 μmol/L desferrioxamine mesylate(DFOM,a strong Fe complexing ligand) was added,the rate of DIC photoproduction fell to 55.6% that of the original SRHA samples with 5.46 μmol/L Fe.

Distribution of Dissolved Inorganic Carbon (DIC) and Its Related Parameters in Seawater of the North Yellow Sea and off the Qingdao Coast in October, 2007

Data on the distribution of dissolved inorganic carbon (DIC) were obtained from two cruises in the North Yellow Sea (NYS) and off the Qingdao Coast (QC) in October, 2007. Carbonate parameters were calculated. The concentrations of DIC are from 1.896-2.229 mmolL-1 in the NYS and from 1.939-2.032 mmolL-1 off the QC. In the southwest of the NYS, DIC in the upper layers decreases from the north of the SP (Shandong Peninsula) shelf to the center of the NYS; whereas in the lower layers DIC increases from the north of the SP shelf to the center of the NYS and South Yellow Sea. In the northeast of the NYS, DIC in all layers in- creases from the YR (Yalu River) estuary to the centre of the NYS. The distribution of DIC in NYS can be used as an indicator of Yellow Sea Cold Water Mass (YSCWM). Air-sea CO2 fluxes were calculated using three models and the results suggest that both the NYS and the QC waters are potential sources of atmospheric CO2 in October.

Sources of dissolved inorganic carbon in rivers from the Changbaishan area, an active volcanic zone in North Eastern China

Major elements and carbon isotopes of dissolved inorganic carbon(DIC)have been measured in the waters of Changbaishan mountain,a volcanic area in northeastern China,between June and September 2016 to decipher the origin of the CO_2 involved in chemical weathering reactions.Spatial variations of major elements ratios measured in water samples can be explained by a change of the chemical composition of the volcanic rocks between the volcanic cone(trachytes)and the basaltic shield as evidenced by the variations in the composition of these rocks.Hence,DIC results from the neutralization of CO_2 by silicate rocks.DIC concentrations vary from 0.3 to 2.5 mmol/L and carbon isotopic compositions of DIC measured in rivers vary from-14.2‰to 3.5‰.At a first order,the DIC transported by rivers is derived from the chemical weathering’s consumption of CO_2 with a magmatic origin,enriched in^(13)C(-5%)and biogenic soil CO_2 with lower isotopic compositions.The highest δ^(13)C values likely result from C isotopes fractionation during CO_2 degassing in rivers.A mass balance based on carbon isotopes suggest that the contribution of magmatic CO_2 varied from less than 20%to more than 70%.Uncertainties in this calculation associated with CO_2 degassing in rivers are difficult to quantify,and the consequence of CO_2 degassing would be an overestimation of the contribution of DIC derived from the neutralization of magmatic CO_2 by silicate rocks.

The influence of macronitrogen (NO_3^- and NH_4^+) addition with U lva pertusa on dissolved inorganic carbon system

The influence of macronitrogen （NO3 and NH＋） addition with Ulva pertusa on dissolved inorganic carbon system in seawater was studied. The results indicate that p（C02） and HCO3 concentration decrease significantly, while pH and CO32- concentration increase significantly. When the con- centration of NO3 was less than 71 μmol/dm3 or NH4＋ was less than 49.7μmol/dm3, dissolved inorganic carbon （DIC） absorption rates by Ulva pertusa generally increased with the increasing of nitrogen concentration. The DIC decreased 151 μmol/dm3 with the addition of 71 μmol/dm3 NO3 and decreased 232 μmol/dm3 with the addition of 49.7 μmol/dm3 NH＋ after the experiment compared with DIC measured without nitrogen addition. A significant negative-correlation was found between Ac（DIC） and growth rate （#） of Ulva pertusa （r =- 0.91, P 〈0.000 1, n=11）. NH＋ had more influence on the species of inorganic carbon system than NO3.

Characteristics of dissolved inorganic carbon in produced water from coalbed methane wells and its geological significance

Based on long-term dynamic tracing of dissolved inorganic carbon(DIC)and stable carbon isotope(δ13CDIC)in produced water from 20 coalbed methane(CBM)wells in western Guizhou,the spatial-temporal dynamic variations ofδ13CDIC of the GP well group produced in multi-layer commingled manner were analyzed,and the relationship between the value ofδ13CDIC and CBM productivity was examined.The produced water samples of typical wells in the GP well group were amplified and sequenced using 16S rDNA,and a geological response model ofδ13CDIC in produced water from CBM wells with multi-coal seams was put forward.The research shows that:δ13CDIC in produced water from medium-rank coal seams commonly show positive anomalies,the produced water contains more than 15 species of methanogens,and Methanobacterium is the dominant genus.The dominant methanogens sequence numbers in the produced water are positively correlated withδ13CDIC,and the positive anomaly of v is caused by reduction of methanogens,and especially hydrogenotrophic methanogens.Vertical segmentation of sedimentary facies and lithology in stratum with multi-coal seams will result in permeability and water cut segmentation,which will lead to the segmentation ofδ13CDIC and archaea community in produced water,so in the strata with better permeability and high water cut,theδ13CDIC of the produced water is abnormally enriched,and the dominant archaea is mainly Methanobacterium.In the strata with weak permeability and low water cut,theδ13CDIC of the produced water is small,and the microbial action is weak.The shallow layer close to the coal seam outcrop is likely to be affected by meteoric precipitation,so theδ13CDIC of the produced water is smaller.The geological response model ofδ13CDIC in produced water from multi-coal seams CBM wells in the medium-rank coal reveals the geological mechanism and microbial action mechanism of theδ13CDIC difference in the produced water from the multi-coal seams CBM wells.It also provides effective geochemical evidence for the superimposed fluid system controlled by sedimentary facies,and can also be used for the contribution analysis of the produced gas and water by the multi-layer CBM wells.

Distributions of dissolved inorganic carbon and total alkalinity in the Western Arctic Ocean

The third Chinese National Arctic Research Expedition （3rd CHINARE-Arctic in 2008） was carried out from July to September 2008. During the survey, numerous sea water samples were taken for CO2 parameter measurement （including total alkalinity TA and total dissolved inorganic carbon DIC）.The distribution of COs parameters in the Western Arctic Ocean was determined, and the controlling factors are addressed. The ranges of summertime TA, normalized TA （nTA）, DIC and normalized DIC （nDIC） in the surface seawater were 1 757 2 229 umol.kg 1 2 383-2 722 umol.kg-1, 1 681 2 034 pmol.kg 1, 2 119--2 600 umol.kg-1, respectively. Because of dilution from ice meltwater, the surface TA and DIC concentrations were relatively low. TA in the upper 100 m to the south of 78°N had good correlation with salinity, showing a conservative behavior. The distribution followed the seawater-river mixing line at salinity 〉30, then followed the seawater mixing line （diluted by river water to salinity = 30） with the ice meltwater. The DIC distribution in the Chukchi Sea was dominated by biological production or respiration of organic matter, whereas conservative mixing dominated the mixed layer TA distribution in the ice-free Canada Basin.

The Correlation between the Variation of Dissolved Inorganic Carbon Content and Cyanobacterial Blooms in Fubao Bay of Dianchi Lake

To explore variation of dissolved inorganic carbon content( DIC) caused by cyanobacterial blooms and provide a basis for formulating effective preventive and control measures of cyanobacterial blooms,the concentration of inorganic carbon and the concentration of planktonic algae were studied by sampling method,and the distribution and variation of the DIC and physicochemical factors in the ecological restoration area of Fubao Bay of Dianchi Lake were analyzed. Results indicated that the distribution of chlorophyll-a was significantly positive correlated with CO_3^(2-)( P < 0. 01) and pH values( P < 0. 05); and the distribution of chlorophyll-a was significantly negative correlated with CO_2( P <0. 01),DIC and HCO_3^-( P < 0. 05). In conclusion,the outbreak and extinction of cyanobacterial blooms is one of the important reasons for the variation of inorganic carbon form and concentration.

Photo-production of dissolved inorganic carbon from dissolved organic matter in contrasting coastal waters in the southwestern Taiwan Strait, China

Photo-production of dissolved inorganic carbon （DIC） from chromophoric dissolved organic matter （CDOM） is an important transformation process in marine carbon cycle, but little is known about this process in Chinese coastal systems. This study investigated an estuarine water sample and a coastal seawater sample from the subtropical waters in southeast of China. Water samples were exposed to natural sunlight and the absorption and fluorescence of CDOM as well as the DIC concentration were measured in the summer of 2009. The estuarine water had higher CDOM level, molecular weight and proportion of humic-like fluorescent components than the seawater that exhibited abundant tryptophan-like fluorescent component. After a 3-day irradiation, the CDOM level decreased by 45% in the estuarine water and 20% in the seawater, accompanied with a decrease in the molecular weight and aromaticity of DOM which was inferred from an increase in the absorption spectral slope parameter. The photo-degradation rates of all the five fluorescent components were also notable, in particular two humic-like components （C4 and C5） were removed by 78% and 69% in the estuarine water and by 69% and 56% in the seawater. The estuarine water had a higher photo-production rate of DIC than the seawater （4.4 vs. 2.5 μmol/（L-day））, in part due to its higher CDOM abundance. The differences in CDOM compositions between the twO types of waters might be responsible for the higher susceptibility of the estuarine water to photo-degradation and hence could also affect the photo-production process of DIC.

Quantifying the sources of dissolved inorganic carbon within the sulfate-methane transition zone in nearshore sediments of Qi'ao Island, Pearl River Estuary, Southern China

The significance of the various biogeochemical pathways that drive carbon cycling and the relative fractions of dissolved inorganic carbon(DIC) produced by these reactions within the sulfate-methane transition zone(SMTZ) are still being debated. Unraveling these processes is important to our understanding of the benthic DIC sources and their contributions to the global carbon cycle. Here, we measure pore water geochemistry(chlorine, sulfate, methane, Ca^(2+), Mg^(2+), DIC and δ^(13)C-DIC) as well as solid geochemistry(sedimentary organic carbon(SOC) and δ^(13)C of SOC) in nearshore sediments from Qi'ao Island in the Pearl River Estuary of the Southern China Sea. Our analysis indicates that SOC originates from the mixing of carbon from terrestrial and marine sources, and that terrestrial materials dominate the net loss of SOC during the degradation of organic matter, especially at sites located near the river outlets. Sulfate reduction via SOC degradation is not appreciable in the upper sediment layer due to conservative mixing-dilution by freshwater. However, below this layer, the anaerobic oxidation of methane(AOM) and methanogenesis occur. Within the SMTZ, the δ^(13)C mass balance shows that the proportions of DIC derived from organoclastic SO_4^(2-) reduction(OSR) and AOM are 50.3% to 66.7% and 0.1% to 17.9%, respectively, whereas methanogenesis contributes 17.0% to 43.9%. This study reveals that the upward diffusion of DIC from ongoing methanogenesis significantly influences carbon cycling within the SMTZ in these estuarine sediments. As a result, we suggest that the plots of the ratio of change in sulfate to change in DIC in pore water should be used with caution when discriminating between sulfate reduction pathways in methane-rich sediments.

Alleviating eutrophication by reducing the abundance of Cyanophyta due to dissolved inorganic carbon fertilization:Insights from Erhai Lake,China

The eutrophication of lakes is a global environmental problem.Regulating nitrogen(N)and phosphorus(P)on phytoplankton is considered to be the most important basis of lake eutrophication management.Therefore,the effects of dissolved inorganic carbon(DIC)on phytoplankton and its role in mitigating lake eutrophication have often been overlooked.In this study,the relationships between phytoplankton and DIC concentrations,carbon isotopic composition,nutrients(N and P),and hydrochemistry in the Erhai Lake(a karst lake)were investigated.The results showed that when the dissolved carbon dioxide(CO_(2)(aq))concentrations in the water were higher than 15μmol/L,the productivity of phytoplankton was controlled by the concentrations of TP and TN,especially by that of TP.When the N and P were sufficient and the CO_(2)(aq)concentrations were lower than 15μmol/L,the phytoplankton productivity was controlled by the concentrations of TP and DIC,especially by that of DIC.Additionally,DIC significantly affected the composition of the phytoplankton community in the lake(p<0.05).When the CO_(2)(aq)concentrations were higher than 15μmol/L,the relative abundance of Bacillariophyta and Chlorophyta was much higher than those of harmful Cyanophyta.Thus,high concentrations of CO_(2)(aq)can inhibit harmful Cyanophyta blooms.

Inorganic Carbon Utilization in Some Marine Phytoplankton Species

In order to learn the ways and possible utilization mechanisms of dissolved inorganic carbon (DIC) in marine phytoplankton species under carbon-replete or -limited conditions, the activity of extracellular carbonic anhydrase (CA) was assayed in different pH, CO 2 and DIC concentrations. Extracellular CA in Amphidinium carterae and Prorocentrum minimum was detected under carbon-replete conditions, while in Melosira sp., Phaeodactylum tricornutum, Skeletonema costatum, Thalassiosira rotula, Emiliania huxleyi and Pleurochrysis carterae, CA activity was assayed under conditions of carbon limitation. No CA activity was found even under carbon-limited conditions in Chaetoceros compressus, Glenodinium foliaceum, Coccolithus pelagicus, Gephrocapsa oceanica and Heterosigma akashiwo. In species without extracellular CA activity, the direct HCO - 3 uptake was investigated using a pH drift technique and the anion exchange inhibitor 4′4′-diisothiocyanatostilbene-2,2-disulfonic acid (DIDS) in a closed system. The result showed that direct HCO - 3 transport might occur by an anion exchange mechanism in species Coc. pelagicus and G. oceanica. Of the 13 species investigated, only H. akashiwo did not have the potential for direct uptake or extracellular CA-catalyzed HCO - 3 utilization.

Inorganic Carbon Parameters Responding to Summer Hypoxia Outside the Changjiang Estuary and the Related Implications

The eutrophication, hypoxia and coastal acidification are attracting more and more attention. In this study, inorganic carbon parameters, including dissolved inorganic carbon （DIC）, total alkalinity （TA） and calculated partial pressure of CO2 （pCO2）, obtained from a summer cruise in August, 2009, were used to investigate their integrated response to biological processes accompanying the oxygen depletion in the areas off the Changjiang Estuary. According to the observations, the typical hypoxia occurred in the bottom water just outside the Changjiang Estuary with Dissolved Oxygen （DO） lower than 2.00 mg L^-1. The biological uptake in the surface water and the decomposition of organic matter in the bottom water were fully coupled with each other. The high concentration of Chl_a （Chl_a = 10.9μgL^-1） and DO （9.25 mgL^-1）, profoundly decreased DIC concentration 0828 μmolkg^-1） and elevated pH （8.42） was observed in the surface water. The correspondingly increased DIC and depletion of oxygen were observed in the bottom water. The semi-quantitative analysis proved that the locally-produced phytoplankton, determined by primary productivity, was deposited to the bottom and contributed about 76% of total amount of the organic carbon decomposition in the bottom. However, in the bottom hypoxia （DO = 2.05 mgL^-1） area observed in the Southern Zhejiang coastal water, the responding patterns of inorganic carbon parameters deviated from the previous one. The expanding of Changjiang Diluted Water （CDW）, the adding of Hangzhou Bay water （with high DIC concentration） and Coastal Current together modify the DIC background value in this area, and the local degeneration and upwelling process may also help to offset the local DIC removed by net biological uptake in surface water. In addition when the mixing occurring in autumn, which may break the summer stratification, the excess release of high DIC in the bottom water to the subsurface water could have an important influence on coastal acidification and the CO2 uptake capacity in this area.

The Effects of Estuarine Processes on the Fluxes of Inorganic and Organic Carbon in the Yellow River Estuary

Riverine carbon flux is an important component of the global carbon cycle. The spatial and temporal variations of organic and inorganic carbon were examined during both dry and wet seasons in the Yellow River estuary. Concentrations of dissolved organic carbon （DOC） and dissolved inorganic carbon （DIC） in the Yellow River during dry seasons were higher than those during wet seasons. The effective concentrations of DOC （CDOC＊） were higher than the observed DOC at zero salinity. This input of DOC in the Yellow River estuary was due to sediment desorption processes in low salinity regions. In contrast to DOC, the effective concen- trations of DIC were 10% lower than the DIC measured at freshwater end, and the loss of DIC was caused by CaCO3 precipitation in low salinity region, Particulate organic carbon （POC） and particulate inorganic carbon （PIC） contents of the particles stabilized to constant values （0.5%：t：0.05% and 1.8%--0.2%, respectively） within the turbidity maximum zone （TMZ） and showed no noticeable seasonal variations. A rapid drop of PIC and rise of POC occurred simultaneously outside the TMZ due to an intense dilution of riv- erine inorganic-rich particles being transported into a pool of aquatic organic-poor particles outside the TMZ. Annually, the Yellow River transported 6.95× 10^5 t of DIC, 0.64× 10^5 t of DOC, 78.58× 10^5 t of PIC and 2.29× 10^5 t of POC to the sea.

RIVERINE INORGANIC CARBON DYNAMICS:OVERVIEW AND PERSPECTIVE

Inorganic carbon, the great part of the riverine carbon exported to the ocean, plays an important role in the global carbon cycle and ultimately impacts the coupled carbon-climate system. An overview was made on both methods and results of the riverine inorganic carbon researches. In addition to routine in situ survey, measurement and calculation, the direct precipitation method and the gas evolution technique were commonly used to analyze dissolved inorganic carbon in natural water samples. Soil CO2, carbonate minerals and atmospheric CO2 incorporated into riverine inorganic car- bon pool via different means, with bicarbonate ion being the dominant component. The concentration of inorganic carbon, the composition of carbon isotopes （8^13C and △^14C）, and their temporal or spatial variations in the streams were controlled by carbon input, output and changes of carbon biogeochemistry within the riverine system. More accurate flux es- timation, better understanding of different influential processes, and quantitative determination of various inputs or outputs need to be well researched in future.

The Response of Carbonate System to Watershed Urbanization Process in a Semi-Arid River

Different from rivers in humid areas,the variability of riverine CO_(2) system in arid areas is heavily impacted by anthropogenic disturbance with the increasing urbanization and water withdrawals.In this study,the water chemistry and the controls of carbonate system in an urbanized river(the Fenhe River)on the semi-arid Loess Plateau were analyzed.The water chemistry of the river water showed that the high dissolved inorganic carbon(DIC)concentration(about 37 mg L^(-1))in the upstream with a karst land type was mainly sourced from carbonate weathering involved by H_(2)CO_(3) and H_(2)SO_(4),resulting in an oversaturated partial pressure of CO_(2)(pCO_(2))(about 800μatm).In comparison,damming resulted in the widespread appearance of non-free flowing river segments,and aquatic photosynthesis dominated the DIC and pCO_(2) spatiality demonstrated by the enriched stable isotope of DIC(δ^(13)CDIC).Especially in the mid-downstream flowing through major cities in warm and low-runoff August,some river segments even acted as an atmospheric CO_(2) sink.The noteworthy is wastewater input leading to a sudden increase in DIC(>55 mg L^(-1))and pCO_(2)(>4500μatm)in the downstream of Taiyuan City,and in cold November the increased DIC even extended to the outlet of the river.Our results highlight the effects of aquatic production induced by damming and urban sewage input on riverine CO_(2) system in semi-arid areas,and reducing sewage discharge may mitigate CO_(2) emission from the rivers.

The Contribution of Nutrients and Water Properties to the Carbonate System in Three Particular Areas of the Tropical Atlantic (NE-BRAZIL)

Tropical waters show different regional aspects due to specificities in their nutrient biogeochemical cycles, which can affect the carbon system and influence their regional role as sinks or sources of CO2. This study was performed on particular tropical areas that present a different seasonal behaviour related to the carbon cycle observed in the late rainy season (July 2013). Understanding the CO2 drawdown and outgassing potential in these areas is needed to call attention to more long-term monitoring efforts and protect understudied tropical coastal systems more efficiently. This study is focused on nutrient values, hydrological data, biogeochemical carbon behaviour linked to the carbonate system and includes estimates of CO2 fluxes in three contrasting areas off the northeastern Brazilian shelf: 1) an urbanised estuary (Recife-REC), 2) a coastal Island (Itamaracá-ITA) and 3) an oceanic archipelago (Fernando de Noronha-FN). In general, REC acted as a source, while ITA and FN as carbon sinks. In ITA, despite the high DIC and Total Alkalinity observed (mean ~2360 μmol·kg-1), the sink is associated with an effective cascading of atmospheric CO2 associated with turbulent shallow waters coupled with biogenic removal of and precipitation of CaCO3 by coralline algae. FN acted as a sink, linked to minor decreases in Total Alkalinity (mean~2295 μmol·kg-1) influenced by ammonium-based primary production, nitrogen fixation and sporadic entrainment of nutrient rich waters in the upper thermocline. More studies in different western tropical Atlantic coastal systems can improve the knowledge of tropical shelf seas and their contribution to the ocean carbon budget under specific regional trophic regimes.

Control factors of DIC in the Y3 seamount waters of the Western Pacific Ocean

An investigation was carried out in the Y3 seamount area of the Western Pacific Ocean in December 2014,and the distribution of dissolved inorganic carbon(DIC)and its relationship with environmental factors in this area were explored.The results show that DIC concentration was higher in the adjacent waters of the Y3 seamount area,and the uplift of DIC isolines at the stations was close to the seamount.Meanwhile,interaction between the North Equatorial Current(NEC)and the Y3 seamount affected the DIC distribution,i.e.,the upwelling in the same direction of the NEC was obvious,resulting in a decreasing trend of average concentration of DIC in the 200 m water column from the top to the two sides in this direction but in the cross direction.The DIC concentration increased with the water depth increase,and its distribution was affected by various environmental factors.In the surface water,high temperature was a decisive factor for the decrease of the DIC concentration,but the photosynthesis of phytoplankton showing only a weak influence.In the North Pacific Tropic Water(NPTW),DIC production rate from organic matter decomposition was higher than that of DIC consumption by phytoplankton photosynthesis,leading to a continual increase of DIC.In the North Pacific Intermediate Water(NPIW),organic matter decomposition played a leading role in the increase of DIC.In the deep water,decomposition of organic matter weakened,and the dissolution of CaCO3 controlled the carbonate system,and DIC had the smallest variation range.

Estimates and Variability of the Air-Sea CO2 Fluxes in the Gulf of Guinea during the 2005-2007 Period

Measurements of CO2 parameters (i.e. Total Alkalinity (TA) and Dissolved Inorganic Carbon (DIC)) were made from June 2005 to September 2007 in six EGEE (“Etude de la circulation océanique et de savariabilitédans le Golfe de GuinEE”) cruises to better assess air-sea CO2 fluxes in the Gulf of Guinea (6°N - 10°S, 10°E - 10°W). Two empirical relationships TA-Salinity and DIC-Salinity-Temperature were established. These relationships were then used to estimate the monthly fugacity of CO2 (fCO2) and air-sea CO2 fluxes. The monthly mean flux of CO2 reaches 1.76 ± 0.82 mmol·m-2·d-1 (resp. 2.90 ± 1.45 mmol·m-2·d-1) at the north of the Equator (resp. at the South). The north-south gradient observed as the patterns of the air-sea CO2 fluxes was mainly driven by the oceanic fCO2. This gradient was due to the low values of the CO2 parameters flowing by the Guinea Current (6°N - 0°) from the west to the east while the air-sea CO2 fluxes increased in the south (10°S - 0). In the north, the climatology of Takahashi underestimated the CO2 fluxes in the Gulf of Guinea when comparing to the estimated fluxes. This was due to the north-south gradient, which did not well reproduce by the climatology of Takahashi.