Increase In Total Alkalinity Research Articles

Implementation and assessment of a model including mixotrophs and the carbonate cycle (Eco3M_MIX-CarbOx v1.0) in a highly dynamic Mediterranean coastal environment (Bay of Marseille, France) – Part 2: Towards a better representation of total alkalinity when modeling the carbonate system and air–sea CO2 fluxes

Abstract. The Bay of Marseille (BoM), located in the northwestern Mediterranean Sea, is affected by various hydrodynamic processes (e.g., Rhône River intrusion and upwelling events) that result in a highly complex local carbonate system. In any complex environment, the use of models is advantageous since it allows us to identify the different environmental forcings, thereby facilitating a better understanding. By combining approaches from two biogeochemical ocean models and improving the formulation of total alkalinity, we develop a more realistic representation of the carbonate system variables at high temporal resolution, which enables us to study air–sea CO2 fluxes and seawater pCO2 variations more reliably. We apply this new formulation to two particular scenarios that are typical for the BoM: (i) summer upwelling and (ii) Rhône River intrusion events. In both scenarios, our model was able to correctly reproduce the observed patterns of pCO2 variability. Summer upwelling events are typically associated with a pCO2 decrease that mainly results from decreasing near-surface temperatures. Furthermore, Rhône River intrusion events are typically associated with a pCO2 decrease, although, in this case, the pCO2 decrease results from a decrease in salinity and an overall increase in total alkalinity. While we were able to correctly represent the daily range of air–sea CO2 fluxes, the present configuration of Eco3M_MIX-CarbOx does not allow us to correctly reproduce the annual cycle of air–sea CO2 fluxes observed in the area. This pattern directly impacts our estimates of the overall yearly air–sea CO2 flux as, even if the model clearly identifies the bay as a CO2 sink, its magnitude was underestimated, which may be an indication of the limitations inherent in dimensionless models for representing air–sea CO2 fluxes.

Rapid shoaling of aragonite saturation horizon in the northern Indian Ocean

Anthropogenic carbon dioxide (CO2) penetrates up to 1000 m of water column in the Indian Ocean resulting in acidification and corrosion of aragonite skeletal material. The shallowest aragonite saturation horizon (ASH) was observed in the Bay of Bengal (BoB; 219 ± 10 m) within the tropical Indian Ocean. The ASH shoaled at the rate of 6.3 ± 5 and 4.4 ± 3 m yr−1 in the past four decades in the BoB and Arabian Sea respectively. As a result, an increase in total alkalinity (TA) was observed at the rate of 0.5 ± 0.3 and 0.25 ± 0.2 μmol kg−1 yr−1 at the depth of ASH in the BoB, and Arabian Sea respectively. While the shoaling rate of ASH remained the same in the Arabian Sea over the past four decades, in contrast, rapid shoaling was observed in the BoB in the recent decades due to higher accumulation of anthropogenic CO2 in the upper ocean associated with an increase in river discharge and decomposition of riverine organic matter. These two processes decreased the pH resulting in corrosion of aragonite skeletal material and increased TA at the depth of ASH in the BoB. Under a business-as-usual scenario, aragonite-secreting organisms will be seriously affected by the middle of this century in the BoB.

The impact of ICE‐6G ice sheet topography in the oceanic carbonate system

AbstractDuring the Last Glacial Maximum (approximately 21 ka BP) the presence of large ice sheets over the Northern Hemisphere (NH) caused significant changes in the ocean–atmosphere interaction. Remarkable changes are noticed in NH both topography and atmospheric CO2 levels. This paper investigates the impact of the most recent paleotopography (ICE6G) in the Earth's climate and the oceanic carbonate system, based on a series of experiments conducted with the oceanic‐atmosphere‐vegetation‐ice‐carbon model, UVic ESCM. Results indicate enhanced cooling in northern North America in the ICE6G compared to the ICE4G simulation due to the lapse rate effect. The decrease of −24°C in the surface temperature in the ICE6G relative to the present day (PD) led to a modification of the atmospheric circulation in the Atlantic and North Pacific regions. Positive and negative anomalies vary widely for the E–P (evaporation–precipitation) flux pattern, but colder and drier atmosphere leads to a reduction in precipitation in the ICE6G experiment. Changes in wind stress between ICE6G and PD induce low temperatures in the Northern Hemisphere. These features are related changes of Ekman's transport and evaporative cooling resulting in positive anomalies of SST. Thus, changes in sea surface temperature and salinity (SST, SSS), and E–P flux led to modifications in the oceanic carbonate system, resulting in an overall increase of total alkalinity and a reduction in the concentrations of total carbon dioxide (TCO2) in the ICE6G with respect to the PD values. This is a consequence of the low concentration of glacial CO2 and increment in concentrations. The total alkalinity (TA) and TCO2 do not show a similar response to the SST and SSS, in the sense that larger departures from the PD are found in the Pacific equatorial region, which are affected by changes in water dilution as a result of precipitation and evaporation processes.

Seasonal Upwelling Conditions Modulate the Calcification Response of a Tropical Scleractinian Coral

Natural processes such as upwelling of deeper-water masses change the physical-chemical conditions of the water column creating localized ocean acidification events that can have an impact on the natural communities. This study was performed in a coral reef system of an archetypical bay within the Tayrona National Natural Park (PNNT) (Colombia), and aimed to quantify net calcification rates of a foundational coral species within a temporal context (6 months) taking into account the dynamics of seasonal upwelling that influence the study area. Net calcification rates of coral fragments were obtained in situ by the alkalinity anomaly technique in short-term incubations (~2.5 h). We found a significant effect of the upwelling on net calcification rates (Gnet) (p < 0.05) with an 42% increase in CaCO3 accretion compared to non-upwelling season. We found an increase in total alkalinity (AT) and dissolved inorganic carbon (DIC) with decreased aragonite saturation (Ωara) for the upwelling months, indicating an influence of the Subtropical Under Water mass (SAW) in the PNNT coral community. Significant negative correlations between net calcification with temperature and Ωara, which indicates a positive response of M. auretenra with the upwelling conditions, thus, acting as “enhancer” of resilience for coral calcification.

Stability of alkalinity in ocean alkalinity enhancement (OAE) approaches – consequences for durability of CO2 storage

Abstract. According to modelling studies, ocean alkalinity enhancement (OAE) is one of the proposed carbon dioxide removal (CDR) approaches with large potential, with the beneficial side effect of counteracting ocean acidification. The real-world application of OAE, however, remains unclear as most basic assumptions are untested. Before large-scale deployment can be considered, safe and sustainable procedures for the addition of alkalinity to seawater must be identified and governance established. One of the concerns is the stability of alkalinity when added to seawater. The surface ocean is already supersaturated with respect to calcite and aragonite, and an increase in total alkalinity (TA) together with a corresponding shift in carbonate chemistry towards higher carbonate ion concentrations would result in a further increase in supersaturation, and potentially to solid carbonate precipitation. Precipitation of carbonate minerals consumes alkalinity and increases dissolved CO2 in seawater, thereby reducing the efficiency of OAE for CO2 removal. In order to address the application of alkaline solution as well as fine particulate alkaline solids, a set of six experiments was performed using natural seawater with alkalinity of around 2400 µmol kgsw−1. The application of CO2-equilibrated alkaline solution bears the lowest risk of losing alkalinity due to carbonate phase formation if added total alkalinity (ΔTA) is less than 2400 µmol kgsw−1. The addition of reactive alkaline solids can cause a net loss of alkalinity if added ΔTA > 600 µmol kgsw−1 (e.g. for Mg(OH)2). Commercially available (ultrafine) Ca(OH)2 causes, in general, a net loss in TA for the tested amounts of TA addition, which has consequences for suggested use of slurries with alkaline solids supplied from ships. The rapid application of excessive amounts of Ca(OH)2, exceeding a threshold for alkalinity loss, resulted in a massive increase in TA (> 20 000 µmol kgsw−1) at the cost of lower efficiency and resultant high pH values > 9.5. Analysis of precipitates indicates formation of aragonite. However, unstable carbonate phases formed can partially redissolve, indicating that net loss of a fraction of alkalinity may not be permanent, which has important implications for real-world OAE application. Our results indicate that using an alkaline solution instead of reactive alkaline particles can avoid carbonate formation, unless alkalinity addition via solutions shifts the system beyond critical supersaturation levels. To avoid the loss of alkalinity and dissolved inorganic carbon (DIC) from seawater, the application of reactor techniques can be considered. These techniques produce an equilibrated solution from alkaline solids and CO2 prior to application. Differing behaviours of tested materials suggest that standardized engineered materials for OAE need to be developed to achieve safe and sustainable OAE with solids, if reactors technologies should be avoided.

Influence of Ammonia Concentration on Solvay Soda Process Parameters and Associated Environmental and Energetic Effects

Modifying the absorption process in soda production by the Solvay method requires performing many calculations and determining a new equilibrium process. An increase in ammonia concentration in the reaction solution causes kinetic changes in equilibrium. Changes to the Solvay soda production technology were determined using chemical and instrumental analysis methods. A modification of the process in the form of SAB was introduced. Information allowing the design of an additional absorber and its location in the network of technological devices was presented in the form of parameters using typical chemical engineering assumptions. Spectroscopic and electrochemical techniques were used for this purpose. The increase in total alkalinity due to the addition of ammonia to 135 mmol·20 cm−3 resulted in cooling savings of about 152.4 MJ·Mg−1 of soda. The ammonia desorption rate and process energy parameters were determined for the new system. The temperature requirements for the carbonation column were defined, and in particular, a technique was developed to minimize the cooling of the lower part of the reactor, which reduces the consumption of process energy. Emissions of CO2 were reduced from 11.70 to 7.85% and NH3 from 5.52 to 4.89% in exhaust gases from the carbonation column.

Glacial state of the global carbon cycle: time-slice simulations for the last glacial maximum with an Earth-system model

Abstract. Three time-slice carbon cycle simulations for the last glacial maximum (LGM) constrained by the CO2 concentration in the atmosphere and the increase in the mean concentration of dissolved inorganic carbon in the deep ocean were carried out with a fully coupled comprehensive climate model (the Community Earth System Model version 1.2). The three modelled LGM ocean states yielded different physical features in response to artificial freshwater forcing, and, depending on the physical states, suitable amounts of carbon and alkalinity were added to the ocean to satisfy constraints from paleo-data. In all the simulations, the amount of carbon added was in line with the inferred transfers of carbon among various reservoirs during the evolution from the LGM to the pre-industrial (PI) period, suggesting that the simulated glacial ocean states are compatible with the PI one in terms of the carbon budget. The increase in total alkalinity required to simulate ocean states that were deemed appropriate for the LGM was in broad quantitative accord with the scenario of post-glacial shallow water deposition of calcium carbonate, although a more precise assessment would demand further studies of various processes such as the land chemical weathering and deep-sea burial of calcium carbonates, which have affected the alkalinity budget throughout history since the LGM. On the other hand, comparisons between the simulated distributions of paleoceanographic tracers and corresponding reconstructions clearly highlighted the different water-mass geometries and favoured a shallower Atlantic meridional overturning circulation (AMOC) for the LGM as compared to PI.

Seasonal Assessment of Chemical and Physical Characterization of Khabur River, Zakho District, Kurdistan Region/Iraq -A Case Study

The river Khabur, the life line of more than 500 thousand of people, supplies water for the important requirements of life. In this work, a total of 192 samples of water were collected at Khabur River, Zakho District. The samples were collected monthly at four different seasons like spring, summer, autumn and winter from March, 2019 to February 2020. The samples of water were examined for total hardness (TH) , total alkalinity (TA), pH, Calcium( Ca2+) , Electrical conductivity (EC), Nitrate (NO3-), total dissolved solids (TDS), Sulfate (SO4 2−) , phosphate, magnesium (Mg2+) BOD, and DO according to the standard methods . The results of the chemical and physical characteristics indicate the water river samples with the following parameters. The total mean values of temperature ranged from (14.461± 14.1469) oC , pH varied from (7.831 ± 0.2842). Conductivity ranged from (560. 25 ±110. 805) µS/cm).Total alkalinity varied from (194.19 ± 69.591) mg/L. Total dissolved solids varied from (355.99 ±71.581) mg/L. Dissolved oxygen varied from (8.219 ± 0.7989) mg/L. Biochemical oxygen Demand (BOD) ranged from (9.857± 6.0760) mg/L. Total hardness varied from ( 535.02 ±78.014) mg/l. Calcium (Ca2+) varied from (409.19 ± 46.875) mg/l. Magnesium (Mg2+) ranged from ( 127.58 ± 46.875) mg/L. Chloride (CL-) varied from ( 26.938 ± 21.2133) mg/L. Nitrate (NO3-) ranged from ( 4.449 ± 2.0327) mg/L. Sulfate (SO4 2−) varied from( 43.24 ±22.479) mg/l. And phosphate ranged from (4.839 ± 1.9139) µg/L. Gradual increase in total alkalinity and hardness towards the downstream is, due to effluents in the Khabur River. Untreated from sewage discharge on river water it causes of high organic matter, phosphate and Nitrate, at high contents in Khabur River .TDS and EC were found moderate in all locations at Khabur River. The total hardness exceeded the permissible limit in all sites. The (Ca2+) and (Mg2+) were exceeded the permissible limit in all sites. In the present study an attempt had been made to determine the levels of wastewater that ultimately discharged into Khabor River without proper treatment.

Bacterial succession along a sediment porewater gradient at Lake Neusiedl in Austria

We provide bacterial 16S rRNA community and hydrochemical data from water and sediments of Lake Neusiedl, Austria. The sediments were retrieved at 5 cm intervals from 30–40 cm push cores. The lake water community was recovered by filtration through a 3.0/0.2 µm filter sandwich. For 16S rRNA gene amplicon-based community profiling, DNA was extracted from the sediment and filters and the bacterial V3-V4 regions were amplified and sequenced using a MiSeq instrument (Illumina). The reads were quality-filtered and processed using open source bioinformatic tools, such as PEAR, cutadapt and VSEARCH. The taxonomy was assigned against the SILVA SSU NR 132 database. The bacterial community structure was visualised in relation to water and porewater chemistry data. The bacterial community in the water column is distinct from the sediment. The most abundant phyla in the sediment shift from Proteobacteria to Chloroflexota (formerly Chloroflexi). Ammonium and total alkalinity increase while sulphate concentrations in the porewater decrease. The provided data are of interest for studies targeting biogeochemical cycling in lake sediments.

Anaerobic microbial activity affects earliest diagenetic pathways of bivalve shells

AbstractThe earliest diagenetic post‐mortem exposure of biogenic carbonates at the sea floor and in the uppermost sediment column results in the colonization of hard‐part surfaces by bacterial communities. Some of the metabolic redox processes related to these communities have the potential to alter carbonate shell properties, and hence affect earliest diagenetic pathways with significant consequences for archive data. During a three‐month in vitro study, shell subsamples of the ocean quahog Arctica islandica (Linnaeus, 1767) were incubated in natural anoxic sediment slurries and bacterial culture medium of the heterotrophic Shewanella sediminisHAW‐EB3. Bulk analyses of the liquid media from the Shewanella sediminis incubation revealed an over ten‐fold increase in total alkalinity, dissolved inorganic carbon and ΩAragonite, and the alteration of the Mg/Ca, Mg/Sr and Sr/Ca ratios relative to control incubations without cultures. Ion ratios were most affected in the incubation with anoxic sediment, depicting a 25% decrease in Mg/Ca relative to the control. Shell sample surfaces that were exposed to both incubations displayed visible surface dissolution features, and an 8 wt% loss in calcium content. No such alteration features were detected in control shells. Apparently, alteration of shell carbonate properties was induced by microbially driven decomposition of shell intercrystalline organic constituents and subsequent opening of pathways for pore fluid–crystal exchange. This study illustrates the potential influence of benthic bacterial metabolism on biogenic carbonate archives during the initial stages of diagenetic alteration within a relatively short experimental duration of only three months. These results suggest that foremost the biological effect of bacterial cation adsorption on divalent cation ratios has the potential to complicate proxy interpretation. Results shown here highlight the necessity to consider bacterial metabolic activities in marine sediments for the interpretation of palaeo‐environmental proxies from shell carbonate archives.

Slow acidification of the winter mixed layer in the subarctic western North Pacific

AbstractWe used carbon dioxide (CO2) system data collected during 1999–2015 to investigate ocean acidification at time series sites in the western subarctic region of the North Pacific Ocean. The annual mean pH at station K2 decreased at a rate of 0.0025 ± 0.0010 year−1 mostly in response to oceanic uptake of anthropogenic CO2. The Revelle factor increased rapidly (0.046 ± 0.022 year−1), an indication that the buffering capacity of this region of the ocean has declined faster than at other time series sites. In the western subarctic region, the pH during the winter decline at a slower rate of 0.0008 ± 0.0004 year−1. This was attributed to a reduced rate of increase of dissolved inorganic carbon (DIC) and an increase of total alkalinity (TA). The reduction of DIC increase was caused by the decline of surface water density associated with the pycnocline depression and the reduction of vertical diffusion flux from the upper pycnocline. These physical changes were probably caused by northward shrinkage of the western subarctic gyre and global warming. Meanwhile, the contribution of the density decline to the TA increase is canceled out by that of the reduced vertical diffusive flux. We speculated that the winter TA increase is caused mainly by the accumulation of TA due to the weakened calcification by organisms during the winter.

Coastal ocean acidification and increasing total alkalinity in the northwestern Mediterranean Sea

Abstract. Coastal time series of ocean carbonate chemistry are critical for understanding how global anthropogenic change manifests in near-shore ecosystems. Yet, they are few and have low temporal resolution. At the time series station Point B in the northwestern Mediterranean Sea, seawater was sampled weekly from 2007 through 2015, at 1 and 50 m, and analyzed for total dissolved inorganic carbon (CT) and total alkalinity (AT). Parameters of the carbonate system such as pH (pHT, total hydrogen ion scale) were calculated and a deconvolution analysis was performed to identify drivers of change. The rate of surface ocean acidification was −0.0028 ± 0.0003 units pHT yr−1. This rate is larger than previously identified open-ocean trends due to rapid warming that occurred over the study period (0.072 ± 0.022 °C yr−1). The total pHT change over the study period was of similar magnitude as the diel pHT variability at this site. The acidification trend can be attributed to atmospheric carbon dioxide (CO2) forcing (59 %, 2.08 ± 0.01 ppm CO2 yr−1) and warming (41 %). Similar trends were observed at 50 m but rates were generally slower. At 1 m depth, the increase in atmospheric CO2 accounted for approximately 40 % of the observed increase in CT (2.97 ± 0.20 µmol kg−1 yr−1). The remaining increase in CT may have been driven by the same unidentified process that caused an increase in AT (2.08 ± 0.19 µmol kg−1 yr−1). Based on the analysis of monthly trends, synchronous increases in CT and AT were fastest in the spring–summer transition. The driving process of the interannual increase in AT has a seasonal and shallow component, which may indicate riverine or groundwater influence. This study exemplifies the importance of understanding changes in coastal carbonate chemistry through the lens of biogeochemical cycling at the land–sea interface. This is the first coastal acidification time series providing multiyear data at high temporal resolution. The data confirm rapid warming in the Mediterranean Sea and demonstrate coastal acidification with a synchronous increase in total alkalinity.

On the problem of the scale and composition of Paleozoic and Mesozoic granitoid magmatism in the Khilok–Vitim fold belt of Central Transbaikalia

The paper presents a study of the gneissic granitoids of the Malkhan Complex and the intruisve granitoids of the Daur and Bichur complexes developed within the Khilok–Vitim fold belt of Central Transbaikalia. In the state geological map, these complexes have been attributed to the Early and Late Paleozoic. New 40Ar/39Ar geochronological data indicate that these rocks are Mesozoic rather than Paleozoic in age, which suggests the much broader manifestation of the Mesozoic granitoid complexes in this area. The studied Mesozoic granitoid massifs exhibit temporal and compositional zoning reflected in a westward decrease in age (from Early to Late Mesozoic) and increase in total alkalinity and potassium content at the appropriate trace-element characteristics. The obtained results of study of the Khilok–Vitim Belt are interpreted in the framework of the model of the formation of domal–cupola structures by the multiple activity of deep thermochemical plumes.

Simulation of carbon dynamics in the Baltic Sea with a 3D model

A full resolved three-dimensional physical–biogeochemical model ERGOM (Ecological ReGional Ocean model) was used to simulate the carbon dynamics in the Baltic Sea. Here, a simple carbon cycle has been included in the model. This was accomplished by the addition of dissolved inorganic carbon and total alkalinity to the model. Model results of the hindcast simulation (1961–2007) are in a good agreement with observations. Lateral gradients of the alkalinity are well reproduced by the model. A net inorganic carbon transport from the Baltic Sea to the Kattegat is in the range of the results of previous studies. Further, two climate projections with different nutrient load scenarios reflecting the possible development of the carbon system dynamics in the Baltic Sea were conducted.Climate scenario simulations (1961–2100) showed a continuous “acidification effect” of the Baltic Sea that mainly is controlled by changing of the atmospheric pCO2. However, changes in pH due to other factors (such as changing temperature, primary production) are different for different regions of the sea. Simulated mean total alkalinity and dissolved inorganic carbon decrease in scenarios of climate change despite the increase of total alkalinity and dissolved inorganic carbon loads. The performed climate simulations show that mean total alkalinity decreases by about 150mmolm−3 and dissolved inorganic carbon by about 80–120mmolm−3. At the same time total alkalinity to salinity relations change in future climate due to that salinity decreases “faster” than alkalinity. Simultaneously, export of the total alkalinity and the dissolved inorganic carbon from the Baltic Sea to the North Sea has the trend to increase from 11% to 18% depending on the climate scenario.

The solubility of fish‐produced high magnesium calcite in seawater

Fish have been shown to produce high (10 to 48 mol %) magnesium calcite as part of the physiological mechanisms responsible for maintaining salt and water balance. The importance of this source to the marine carbon cycle is only now being considered. In this paper, we report the first measurements of the solubility of this CaCO3 in seawater. The resulting solubility (pK*sp = 5.89 ± 0.09) is approximately two times higher than aragonite and similar to the high magnesium calcite generated on the Bahamas Banks (pK*sp = 5.90). This high solubility of fish‐produced CaCO3 is a result of the high magnesium content and not a product of micro‐environments created by microbial activity. This material is soluble in near surface waters, contributing to the input of carbonate to surface ocean waters, and may at least partially explain the observed increase in total alkalinity above the aragonite saturation horizon.

Evolution of Jurassic–Cretaceous magmatism in the Khambin volcanotectonic complex ( western Transbaikalia)

The Khambin volcanotectonic complex is a horst framing the Late Cretaceous Lake Gusinoe basin in the northwest. This complex is due to the intracontinental rift conditions which existed in western Transbaikalia in the Late Mesozoic. They gave rise to a system of subparallel grabens and horsts in present-day topography. The magmatic evolution of this complex spans from 159 to 117 Ma and is divided into three stages. The first stage (159–156 Ma) witnessed the formation of thick (up to 1500 m) volcanic masses of trachybasalts, basaltic trachyandesites, trachytes, trachydacites, trachyrhyolites, and pantellerites. The next two stages were the formation of isolated ancient volcanoes (127–124 Ma) composed of trachybasalts, basaltic trachyandesites, phonotephrites, tephriphonolites, and alkali trachytes and the formation of the Murtoi (Lake Gusinoe) essexite dike (122–117 Ma). The main trends for igneous associations from early to late stages are reduced magmatism and reduced rock diversity because of the decreasing portion of felsic volcanic rocks. Mafic rocks show an increase in total alkalinity, the content of incompatible elements (Th, U, K, Rb, Pb, Nb, Ta, Zr, Hf), total REE content, and the LREE/HREE ratio. The Sr–Nd isotopic composition of these rocks remained nearly constant and corresponds to that of OIB-EMII mantle sources. Compositional variations are attributed to a time-dependent decrease in the degree of partial melting of a similar magma source.

A model for predicting changes in the electrical conductivity, practical salinity, and absolute salinity of seawater due to variations in relative chemical composition

Abstract. Salinity determination in seawater has been carried out for almost 30 years using the Practical Salinity Scale 1978. However, the numerical value of so-called practical salinity, computed from electrical conductivity, differs slightly from the true or absolute salinity, defined as the mass of dissolved solids per unit mass of seawater. The difference arises because more recent knowledge about the composition of seawater is not reflected in the definition of practical salinity, which was chosen to maintain historical continuity with previous measures, and because of spatial and temporal variations in the relative composition of seawater. Accounting for these spatial variations in density calculations requires the calculation of a correction factor δSA, which is known to range from 0 to 0.03 g kg−1 in the world oceans. Here a mathematical model relating compositional perturbations to δSA is developed, by combining a chemical model for the composition of seawater with a mathematical model for predicting the conductivity of multi-component aqueous solutions. Model calculations for this estimate of δSA, denoted δSRsoln, generally agree with estimates of δSA based on fits to direct density measurements, denoted δSRdens, and show that biogeochemical perturbations affect conductivity only weakly. However, small systematic differences between model and density-based estimates remain. These may arise for several reasons, including uncertainty about the biogeochemical processes involved in the increase in Total Alkalinity in the North Pacific, uncertainty in the carbon content of IAPSO standard seawater, and uncertainty about the haline contraction coefficient for the constituents involved in biogeochemical processes. This model may then be important in constraining these processes, as well as in future efforts to improve parameterizations for δSA.

Decadal change of dissolved inorganic carbon in the subarctic western North Pacific Ocean

Dissolved inorganic carbon (DIC) was measured from 1992 to 2008 at two time-series sites in the subarctic western North Pacific; this region is a source of atmospheric CO2 in winter due to vertical mixing of deep waters rich in DIC. To estimate the decadal DIC increase resulting from CO2 uptake from the atmosphere, we corrected DIC for the contribution of biological activity below the temperature minimum (Tmin) layer (¡«100 m), which is the remnant of the mixed layer from the preceding winter. Decadal DIC increases in the Tmin layer and upper intermediate water (1.3¨C1.5 ¦Ìmol kg-1 yr-1; 100¨C200 m) were higher than those expected from oceanic equilibration with increasing atmospheric CO2 and those previously reported in the open North Pacific. The increase in water column CO2 was estimated to be 0.40 ¡À 0.08 mol m-2 yr-1. The decadal DIC change in the Tmin layer affects winter CO2 emission. The increase of atmospheric xCO2 in winter (2.1 ± 0.0 ppm yr-1) is higher than that of oceanic CO2 (0.7 ¡À 0.5 ppm yr-1) that calculated from DIC and total alkalinity in the Tmin layer. This difference suggests reduction of CO2 emission in winter is possibly controlled by the increase of total alkalinity.

Oxic/anoxic oscillations and organic carbon mineralization in an estuarine maximum turbidity zone (The Gironde, France)

The study of vertical particle dynamics in the highly turbid Gironde Estuary has shown intense cycles of sedimentation and resuspension at both diurnal and neap‐spring time scales. Fluid mud, with suspended particulate matter (SPM) concentrations between 50 and 500 g liter−1, has been observed during neap tides. Vertical profiles of biogeochemical parameters have been measured in the fluid mud. Anoxic conditions have been detected when SPM concentration exceeded 50 g liter−1 in the upstream and 140 g liter−1 in the downstream parts of the maximum turbidity zone (MTZ). At the downstream part of the MTZ, anoxic fluid mud was partitioned into a denitrification layer (SPM = 140−250 g liter−1), intensively reworked at the tidal time scale, and by an Mn(IV)‐reduction layer (SPM > 250 g liter−1) preferentially reworked at the neap spring time scale. Due to the alternation of sedimentation and resuspension periods, most of the sediment experienced oxic/anoxic oscillations throughout the neap‐spring cycle. Fluid mud resuspension occurred without any observable incidence on the surface‐water oxygenation. An increase in total alkalinity was found in the fluid mud, due to both anaerobic respiration and a carbonate dissolution coupled to aerobic respiratory CO2 generation. This phenomenon significantly affected the inorganic carbon budget of the estuary, increasing the HCO3− input to the coastal ocean and reducing the CO2 flux to the atmosphere. An accumulation of labile dissolved organic carbon observed in the fluid mud suggests that these oscillations result in an acceleration of particulate organic matter (POM) decomposition. In the Gironde MTZ, a net loss of refractory land‐derived POM occurs. This system acts as an efficient oxic/suboxic “fluidized bed reactor,” similar to mobile deltaic muds.

Functional polarity of the tentacle of the sea anemone Anemonia viridis: role in inorganic carbon acquisition.

The oral epithelial layers of anthozoans have a polarized morphology: photosynthetic endosymbionts live within endodermal cells facing the coelenteric cavity and are separated from the external seawater by the ectodermal layer and the mesoglea. To study if this morphology plays a role in the supply of inorganic carbon for symbiont photosynthesis, we measured the change in pH and the rate of OH- (H+) fluxes induced by each cell layer on a tentacle of the sea anemone Anemonia viridis. Light-induced pH increase of the medium bathing the endodermal layers led to the generation of a transepithelial pH gradient of approximately 0.8 pH units across the tentacle, whereas darkness induced acidification of this medium. The light-induced pH change was associated with an increase of total alkalinity. Only the endodermal layer was able to induce a net OH- secretion (H+ absorption). The light-induced OH- secretion by the endodermal cell layer was dependent on the presence of HCO3- in the compartment facing the ectoderm and was sensitive to several inhibitors of ion transport. [14C] HCO3- incorporation into photosynthates confirmed the ectodermal supply, the extent of which varied from 25 to > 90%, according to HCO3- availability. Our results suggest that the light-induced OH- secretion by the endodermal cell layer followed the polarized transport of HCO3- and its subsequent decarboxylation within the endodermal cell layer. This polarity may play a significant role both in inorganic carbon absorption and in the control of light-enhanced calcification in scleractinian corals.