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1.
Early Archean (3.46 Ga) hydrothermally altered basaltic rocks exposed near Marble Bar, eastern Pilbara Craton, have been studied in order to reveal geological and geochemical natures of seafloor hydrothermal carbonatization and to estimate the CO2 flux sunk into the altered oceanic crust by the carbonatization. The basaltic rocks are divided into basalt and dolerite, and the basalt is further subdivided into type I, having original igneous rock textures, and type II, lacking these textures due to strong hydrothermal alteration. Primary clinopyroxene phenocrysts are preserved in some part of the dolerite samples, and the alteration mineral assemblage of dolerite (chlorite + epidote + albite + quartz ± actinolite) indicates that the alteration condition was typical greenschist facies. In other samples, all primary minerals were completely replaced by secondary minerals, and the alteration mineral assemblage of the type I and type II basalts (chlorite + K-mica + quartz + carbonate minerals ± albite) is characterized by the presence of K-mica and carbonate minerals and the absence of Ca-Al silicate minerals such as epidote and actinolite, suggesting the alteration condition of high CO2 fugacity. The difference of the alteration mineral assemblages between basalt and dolerite is probably attributed to the difference of water/rock ratio that, in turn, depends on their porosity.Carbonate minerals in the carbonatized basalt include calcite, ankerite, and siderite, but calcite is quite dominant. The δ13C values of the carbonate minerals are −0.3 ± 1.2‰ and mostly within the range of marine carbonate, indicating that the carbonate minerals were formed by seafloor hydrothermal alteration and that carbonate carbon in the altered basalt was derived from seawater. Whole-rock chemical composition of the basaltic rocks is essentially similar to that of modern mid-ocean ridge basalt (MORB) except for highly mobile elements such as K2O, Rb, Sr, and Ba. Compared to the least altered dolerite, all altered basalt samples are enriched in K2O, Rb, and Ba, and are depleted in Na2O, reflecting the presence of K-mica replacing primary plagioclase. In addition, noticeable CO2 enrichment is recognized in the basalt due to the ubiquitous presence of carbonate minerals, but there was essentially neither gain nor loss of CaO. This suggests that the CO2 in the hydrothermal fluid (seawater) was trapped by using Ca originally contained in the basalt. The CaO/CO2 ratios of the basalt are generally the same as that of pure calcite, indicating that Ca in the basalt was almost completely converted to calcite during the carbonatization, although Mg and Fe were mainly redistributed into noncarbonate minerals such as chlorite.The carbon flux into the Early Archean oceanic crust by the seafloor hydrothermal carbonatization is estimated to be 3.8 × 1013 mol/yr, based on the average carbon content of altered oceanic crust of 1.4 × 10-3 mol/g, the alteration depth of 500 m, and the spreading rate of 1.8 × 1011 cm2/yr. This flux is equivalent to or greater than the present-day total carbon flux. It is most likely that the seafloor hydrothermal carbonatization played an important role as a sink of atmospheric and oceanic CO2 in the Early Archean.  相似文献   

2.
Acidification of surface seawater owing to anthropogenic activities has raised serious concerns on its consequences for marine calcifying organisms and ecosystems. To acquire knowledge concerning the future consequences of ocean acidification (OA), researchers have relied on incubation experiments with organisms exposed to future seawater conditions, numerical models, evidence from the geological record, and recently, observations from aquatic environments exposed to naturally high CO2 and low pH, e.g., owing to volcanic CO2 vents, upwelling, and groundwater input. In the present study, we briefly evaluate the distribution of dissolved CO2–carbonic acid parameters at (1) two locations in the Pacific and the Atlantic Ocean as a function of depth, (2) a mangrove environment in Bermuda, (3) a seasonally stratified body of water in a semi-enclosed sound in Bermuda, and (4) in temporarily isolated tide pools in Southern California. We demonstrate that current in situ conditions of seawater pCO2, pH, and CaCO3 saturation state (Ω) in these environments are similar or even exceed the anticipated changes to these parameters in the open ocean over the next century as a result of OA. The observed differences between the Pacific and Atlantic Oceans with respect to seawater CO2–carbonic acid chemistry, preservation of CaCO3 minerals, and the occurrence and distribution of deep-sea marine calcifiers, support the hypothesized negative effects of OA on the production and preservation of CaCO3 in surface seawater. Clues provided from shallow near-shore environments in Bermuda and Southern California support these predictions, but also highlight that many marine calcifiers already experience relatively high seawater pCO2 and low pH conditions.  相似文献   

3.
We present results from a long term geochemical cycling model, with a focus on the sensitivity of atmospheric carbon dioxide, oxygen, and the major element composition of seawater to seafloor spreading rates. This model incorporates rock weathering, basalt–seawater exchange reactions, and the formation and destruction of chemical sediments and organic matter. Hydrothermal reactions between seafloor and seawater involving calcium, magnesium, sodium, potassium, sulfate and carbon are the high temperature counterparts to low temperature redox, weathering, precipitation and diagenetic reactions. A major source of uncertainty is the extent to which these exchange fluxes are controlled by seafloor spreading rate. In addition, the return fluxes of these components to the atmospheric and primary silicate reservoirs reflect not only the overall rates of subduction and metamorphism, but the distribution of the overlying sedimentary burden and authigenic minerals formed during basalt alteration as well. In particular, we show how the stoichiometry of exchange fluxes (Mg/Ca and SO4/Ca) may buffer atmospheric CO2 and O2 concentrations.  相似文献   

4.
The paired chemical reactions, Ca2+ + 2HCO3 ? ? CaCO3 + CO2 + H2O, overestimate the ratio of CO2 flux to CaCO3 flux during the precipitation or dissolution of CaCO3 in seawater. This ratio, which has been termed ??, is about 0.6 in surface seawater at 25°C and at equilibrium with contemporary atmospheric CO2 and increases towards 1.0 as seawater cools and pCO2 increases. These conclusions are based on field observations, laboratory experiments, and equilibrium calculations for the seawater carbonate system. Yet global geochemical modeling indicates that small departures of ?? from 1.0 would cause dramatic, rapid, and unrealistic change in atmospheric CO2. ?? can be meaningfully calculated for a water sample whether or not it is in equilibrium with the atmosphere. The analysis presented here demonstrates that the atmospheric CO2 balance can be maintained constant with respect to seawater CaCO3 reactions if one considers the difference between CaCO3 precipitation and burial and differing values for ?? (both <1.0) in regions of precipitation and dissolution within the ocean.  相似文献   

5.
Dolomite Controls on Phanerozoic Seawater Chemistry   总被引：1，自引：0，他引：1  
We investigate the potential role of dolomite as a long-term buffer on Phanerozoic seawater composition. Using a comprehensive model of Phanerozoic geochemical cycling, we show how variations in the formation rate of sedimentary marine dolomite have buffered seawater saturation state. The total inventory of inorganic carbon reflects the sum of fluxes derived from continental weathering, basalt-seawater exchange, alumino-silicate diagenesis (reverse weathering), and global deposition of calcium carbonate. Although these fluxes are approximately balanced, model results indicate that seawater saturation state is sensitive to the marine dolomite depositional flux. This conclusion is consistent with and constrained by independent proxy data for seawater ion ratios, paleo-atmospheric CO2 concentrations, and paleo-pH data, and dolomite mass-age distribution through Phanerozoic time. Abundant research indicates that dolomite’s occurrence in marine sediments is sensitive to many factors: temperature, seawater composition, paleogeographic setting, continental organization, etc. Although the complexity of the process of dolomite formation prevents a complete understanding of the relative role of these factors, our model results clearly underscore the importance of this mineral in the chemical history of Phanerozoic seawater.  相似文献   

6.
Instead of having been more or less constant, as once assumed, it is now apparent that the major ion chemistry of the oceans has varied substantially over time. For instance, independent lines of evidence suggest that calcium concentration ([Ca2+]) has approximately halved and magnesium concentration ([Mg2+]) approximately doubled over the last 100 million years. On the other hand, the calcite compensation depth, and hence the CaCO3 saturation, has varied little over the last 100 My as documented in deep sea sediments. We combine these pieces of evidence to develop a proxy for seawater carbonate ion concentration ([CO32−]) over this period of time. From the calcite saturation state (which is proportional to the product of [Ca2+] times [CO32−], but also affected by [Mg2+]), we can calculate seawater [CO32−]. Our results show that [CO32−] has nearly quadrupled since the Cretaceous. Furthermore, by combining our [CO32−] proxy with other carbonate system proxies, we provide calculations of the entire seawater carbonate system and atmospheric CO2. Based on this, reconstructed atmospheric CO2 is relatively low in the Miocene but high in the Eocene. Finally, we make a strong case that seawater pH has increased over the last 100 My.  相似文献   

7.
The Mid-Brunhes dissolution interval (MBDI) represents a period of global carbonate dissolution, lasting several hundred thousand years, centred around Marine Isotope Stage (MIS) 11. Here we report the effects of dissolution in ODP core 982, taken from 1134 m in the North Atlantic. Paradoxically, records of atmospheric CO2 from Antarctic ice-cores reveal no long term trend over the last 400 kyr and suggest that CO2 during MIS 11 was no higher than during the present interglacial. We suggest that a global increase in pelagic carbonate production during this period, possibly related to the proliferation of the Gephyrocapsa coccolithophore, could have altered marine carbonate chemistry in such a way as to drive increased dissolution under the constraints of steady state. An increase in the production of carbonate in surface waters would cause a drawdown of global carbonate saturation and increase dissolution at the seafloor. In order to reconcile the record of atmospheric CO2 variability we suggest that an increase in the flux of organic matter from the surface to deep ocean, associated with either a net increase in primary production or the enhanced ballasting effect provided by an increased flux of CaCO3, could have countered the effect of increased calcification on CO2.  相似文献   

8.
A significant portion of calcium carbonate is deposited in lake sediments as a result of biological processes related to the photosynthetic activity of phytoplankton in the pelagic realm and, in addition, macrophytes in the littoral zone. Lake Wigry, one of the largest lakes in Poland (north‐east Poland), is characterized by: (i) carbonate sediments with a CaCO3 content exceeding 80% within the littoral zone; and (ii) large areas of submerged vegetation dominated by charophytes (macroscopic green algae, Characeae family). It is claimed that charophytes are highly effective in utilizing HCO3? and forming thick CaCO3 encrustations. Thus, this study was aimed at evaluating the CaCO3 production by dense Chara stands overgrowing the lake bottom reaching a depth of 4 m. In late July 2009, the fresh and dry mass of plants, the percentage contribution of calcium carbonate and the production of CaCO3 per 1 m2 were investigated along three transects at three depths (1 m, 2 m and 3 m, with each sample area equal to 0·0625 m2) per transect. The composition and structure of phytoplankton and the physico‐chemical properties of the water analysed in both the littoral and pelagic zones served as the environmental background and demonstrated moderately low fertility in the lake. The greatest dry plant mass exceeded 1000 g m?2 and CaCO3 encrustations constituted from 59% to over 76% of the charophyte dry weight. Thus, the maximum and average values of carbonates precipitated by charophytes were 685·5 and 438 g m?2, respectively, which exceeded previously reported results. A correlation of carbonate production with the depth of Chara stands was detected, and intermediate depths offered the most favourable conditions for carbonate precipitation (589 g m?2 on average). As precipitated carbonates are ultimately stored in bottom deposits, the results highlight the significance of charophytes in lacustrine CaCO3 sedimentation.  相似文献   

9.
Release of CO2 from surface ocean water owing to precipitation of CaCO3 and the imbalance between biological production of organic matter and its respiration, and their net removal from surface water to sedimentary storage was studied by means of a quotient θ = (CO2 flux to the atmosphere)/(CaCO3 precipitated). θ depends not only on water temperature and atmospheric CO2 concentration but also on the CaCO3 and organic carbon masses formed. In CO2 generation by CaCO3 precipitation, θ varies from a fraction of 0.44 to 0.79, increasing with decreasing temperature (25 to 5°C), increasing atmospheric CO2 concentration (195–375 ppmv), and increasing CaCO3 precipitated mass (up to 45% of the initial DIC concentration in surface water). Primary production and net storage of organic carbon counteracts the CO2 production by carbonate precipitation and it results in lower CO2 emissions from the surface layer. When atmospheric CO2 increases due to the ocean-to-atmosphere flux rather than remaining constant, the amount of CO2 transferred is a non-linear function of the surface layer thickness because of the back-pressure of the rising atmospheric CO2. For a surface ocean layer approximated by a 50-m-thick euphotic zone that receives input of inorganic and organic carbon from land, the calculated CO2 flux to the atmosphere is a function of the CaCO3 and Corg net storage rates. In general, the carbonate storage rate has been greater than that of organic carbon. The CO2 flux near the Last Glacial Maximum is 17 to 7×1012 mol/yr (0.2–0.08 Gt C/yr), reflecting the range of organic carbon storage rates in sediments, and for pre-industrial time it is 38–42×1012 mol/yr (0.46–0.50 Gt C/yr). Within the imbalanced global carbon cycle, our estimates indicate that prior to anthropogenic emissions of CO2 to the atmosphere the land organic reservoir was gaining carbon and the surface ocean was losing carbon, calcium, and total alkalinity owing to the CaCO3 storage and consequent emission of CO2. These results are in agreement with the conclusions of a number of other investigators. As the CO2 uptake in mineral weathering is a major flux in the global carbon cycle, the CO2 weathering pathway that originates in the CO2 produced by remineralization of soil humus rather than by direct uptake from the atmosphere may reduce the relatively large imbalances of the atmosphere and land organic reservoir at 102–104-year time scales.  相似文献   

10.
Cold springs upwelling through large serpentinite mud volcanoes in the outer half of the Mariana forearc provide a unique window into processes of devolatilization of the subducting Pacific Plate. We have sampled upwelling pore waters with lower chlorinity than seawater from six sites on five serpentinite mud volcanoes, by conventional gravity and piston coring, by push coring from the ROV Jason, by drilling on ODP Legs 125 and 195, and by manned submersible. The sites range from 13°47′N to 19°33′N and 52 to 90 km from the Mariana trench axis, corresponding to approximate depths to the top of the downgoing plate of 16 to 29 km. The composition of the springs varies systematically over this distance: nearer the trench the upwelling waters have much higher Ca and Sr than seawater and much lower carbonate alkalinity, sulfate, Na/Cl, K, Rb, and B. Farther from the trench the waters show the opposite trends relative to seawater. Chlorinity is consistently lower than in seawater and shows large variations that are not systematic with distance from the trench. Cs is consistently higher than in seawater and increases with distance from the trench. All of the waters have high pH and are heavily depleted in Mg, Si, Li, F, and 87Sr/86Sr relative to seawater. They tend to be enriched in O18/O16. Except for ODP drilling, none of the cores was long enough to produce an asymptotic compositional trend with depth. We have inferred the end-member compositions of the upwelling waters by extrapolation against Mg. At two sites we were able to compare data from gravity cores with data from drill cores or push cores collected at springs to estimate the effects of reactions that occur at shallow depth below the seafloor, on mixing of the upwelling waters with seawater. These effects are different for sites high in dissolved Ca, nearer the trench, vs. those high in alkalinity, farther from the trench. Common to both are large losses from solution of 1) Ca, as CaCO3 and in exchange for Na; 2) Mg, in exchange for Na or Ca and as brucite; 3) sulfate, probably reduced by microbes or possibly precipitated as gypsum; 4) Sr, Ba, Si, and F. Na is consistently leached from the solids into solution, whereas K and O18/O16 are relatively unreactive.We infer that the upwelling waters are uniformly saturated with CaCO3 and that the excess H2O and the trends in Ca, Sr, alkalinity, and sulfate with distance from the trench result from introduction of H2O and dissolved carbonate and sulfate from an external source, the sediment and altered basalt at the top of the subducting plate. The concurrent trends in Na/Cl, B, Cs, and especially K and Rb indicate that these species originate from the top of the subducting plate in response to increasing temperature. These systematic variations across the outer forearc imply that the solutions ascend more or less vertically from the source region and do not travel long distances laterally along the décollement before ascending. Based on leaching of K, the 150°C isotherm is crossed approximately beneath Big Blue Seamount at a depth of ∼22 km below the seafloor, 70 km behind the trench. By this point it appears that carbonate dissolution has joined dehydration as a significant process at the top of the subducting plate.  相似文献   

11.
Rising atmospheric pCO2 and ocean acidification originating from human activities could result in increased dissolution of metastable carbonate minerals in shallow-water marine sediments. In the present study, in situ dissolution of carbonate sedimentary particles in Devil’s Hole, Bermuda, was observed during summer when thermally driven density stratification restricted mixing between the bottom water and the surface mixed layer and microbial decomposition of organic matter in the subthermocline layer produced pCO2 levels similar to or higher than those levels anticipated by the end of the 21st century. Trends in both seawater chemistry and the composition of sediments in Devil’s Hole indicate that Mg-calcite minerals are subject to selective dissolution under conditions of elevated pCO2. The derived rates of dissolution based on observed changes in excess alkalinity and estimates of vertical eddy diffusion ranged from 0.2 mmol to 0.8 mmol CaCO3 m−2 h−1. On a yearly basis, this range corresponds to 175–701 g CaCO3 m−2 year−1; the latter rate is close to 50% of the estimate of the current average global coral reef calcification rate of about 1,500 g CaCO3 m−2 year−1. Considering a reduction in marine calcification of 40% by the year 2100, or 90% by 2300, as a result of surface ocean acidification, the combination of high rates of carbonate dissolution and reduced rates of calcification implies that coral reefs and other carbonate sediment environments within the 21st and following centuries could be subject to a net loss in carbonate material as a result of increasing pCO2 arising from burning of fossil fuels.  相似文献   

12.
The production of organic matter and calcium carbonate by a dense population of the brittle star Acrocnida brachiata (Echinodermata) was calculated using demographic structure, population density, and relations between the size (disk diameter) and the ash-free dry weight (AFDW) or the calcimass. During a 2-year survey in the Bay of Seine (Eastern English Channel, France), organic production varied from 29 to 50 gAFDW m−2 year−1 and CaCO3 production from 69 to 104 gCaCO3 m−2 year−1. Respiration was estimated between 1.7 and 2.0 molCO2 m−2 year−1. Using the molar ratio (ψ) of CO2 released: CaCO3 precipitated, this biogenic precipitation of calcium carbonate would result in an additional release between 0.5 and 0.7 molCO2 m−2 year−1 that represented 23% and 26% of total CO2 fluxes (sum of calcification and respiration). The results of the present study suggest that calcification in temperate shallow environments should be considered as a significant source of CO2 to seawater and thus a potential source of CO2 to the atmosphere, emphasizing the important role of the biomineralization (estimated here) and dissolution (endoskeletons of dead individuals) in the carbon budget of temperate coastal ecosystems.  相似文献   

13.
This paper deals with dissolved inorganic carbon (DIC) and organic carbon (DOC) in pore waters from a 150 m deep hole drilled through the carbonate barrier reef of Tahiti and its underlying basalt basement. Alkalinity-pH measurements were used to calculate the DIC species concentration, and DOC was analysed according to the high temperature catalytic oxidation technique. Salinity was used as a conservative tracer to help identify water origin and mixing within the hole. Water mixing, calcium carbonate dissolution and mineralization of organic carbon combined to form three distinct groups of pore water. In the deeper basalt layers, pore water with alkalinity of 1.4 meq kg–1 pH of 7.6 and p(CO2) of 1.2 mAtm was undersaturated with respect to both aragonite and calcite. In the intermediate carbonate layer, pore water with alkalinity of more than 2.0 meq kg–1, pH of 7.70 and p(CO2) of 1.4 mAtm was supersaturated with respect to both aragonite and calcite. The transition zone between those two groups extended between 80 and 100 m depth. The shift from aragonite undersaturation to supersaturation was mainly attributed to the mixing of undersaturated pore waters from the basalt basement with supersaturated pore waters from the overlaying limestone. In the top of the reef, inputs from a brackish water lens further increased p(CO2) up to 5.6 times the atmospheric P(CO2).  相似文献   

14.
This paper deals with dissolved inorganic carbon (DIC) and organic carbon (DOC) in pore waters from a 150 m deep hole drilled through the carbonate barrier reef of Tahiti and its underlying basalt basement. Alkalinity-pH measurements were used to calculate the DIC species concentration, and DOC was analysed according to the high temperature catalytic oxidation technique. Salinity was used as a conservative tracer to help identify water origin and mixing within the hole. Water mixing, calcium carbonate dissolution and mineralization of organic carbon combined to form three distinct groups of pore water. In the deeper basalt layers, pore water with alkalinity of 1.4 meq kg?1 pH of 7.6 and p(CO2) of 1.2 mAtm was undersaturated with respect to both aragonite and calcite. In the intermediate carbonate layer, pore water with alkalinity of more than 2.0 meq kg?1, pH of 7.70 and p(CO2) of 1.4 mAtm was supersaturated with respect to both aragonite and calcite. The transition zone between those two groups extended between 80 and 100 m depth. The shift from aragonite undersaturation to supersaturation was mainly attributed to the mixing of undersaturated pore waters from the basalt basement with supersaturated pore waters from the overlaying limestone. In the top of the reef, inputs from a brackish water lens further increased p(CO2) up to 5.6 times the atmospheric P(CO2).  相似文献   

15.
《Geochimica et cosmochimica acta》1999,63(13-14):2001-2007
Stable oxygen isotope ratios of foraminiferal calcite are widely used in paleoceanography to provide a chronology of temperature changes during ocean history. It was recently demonstrated that the stable oxygen isotope ratios in planktonic foraminifera are affected by changes of the seawater chemistry carbonate system: the δ18O of the foraminiferal calcite decreases with increasing CO32− concentration or pH. This paper provides a simple explanation for seawater chemistry dependent stable oxygen isotope variations in the planktonic foraminifera Orbulina universa which is derived from oxygen isotope partitioning during inorganic precipitation. The oxygen isotope fractionation between water and the dissolved carbonate species S = [H2CO3] + [HCO3−] + [CO32−] decreases with increasing pH. Provided that calcium carbonate is formed from a mixture of the carbonate species in proportion to their relative contribution to S, the oxygen isotopic composition of CaCO3 also decreases with increasing pH. The slope of shell δ18O vs. [CO32−] of Orbulina universa observed in culture experiments is −0.0022‰ (μmol kg−1)−1 (Spero et al., 1997), whereas the slope derived from inorganic precipitation is −0.0024‰ (μmol kg−1)−. The theory also provides an explanation of the nonequilibrium fractionation effects in synthetic carbonates described by Kim and O’Neil (1997) which can be understood in terms of equilibrium fractionation at different pH. The results presented here emphasize that the oxygen isotope fractionation between calcium carbonate and water does not only depend on the temperature but also on the pH of the solution from which it is formed.  相似文献   

16.
The present analysis adjusts previous estimates of global ocean CaCO3 production rates substantially upward, to 133 × 1012 mol yr?1 plankton production and 42 × 1012 mol yr?1 shelf benthos production. The plankton adjustment is consistent with recent satellite-based estimates; the benthos adjustment includes primarily an upward adjustment of CaCO3 production on so-called carbonate-poor sedimentary shelves and secondarily pays greater attention to high CaCO3 mass (calcimass) and turnover of shelf communities on temperate and polar shelves. Estimated CaCO3 sediment accumulation rates remain about the same as they have been for some years: ~20 × 1012 mol yr?1 on shelves and 11 × 1012 mol yr?1 in the deep ocean. The differences between production and accumulation of calcareous materials call for dissolution of ~22 × 1012 mol yr?1 (~50 %) of shelf benthonic carbonate production and 122 × 1012 mol yr?1 (>90 %) of planktonic production. Most CaCO3 production, whether planktonic or benthonic, is assumed to take place in water depths of <100 m, while most dissolution is assumed to occur below this depth. The molar ratio of CO2 release to CaCO3 precipitation (CO2↑/CaCO3↓) is <1.0 and varies with depth. This ratio, Ψ, is presently about 0.66 in surface seawater and 0.85 in ocean waters deeper than about 1000 m. The net flux of CO2 associated with CaCO3 reactions in the global ocean in late preindustrial time is estimated to be an apparent influx from the atmosphere to the ocean, of +7 × 1012 mol C yr?1, at a time scale of 102–103 years. The CaCO3-mediated influx of CO2 is approximately offset by CO2 release from organic C oxidation in the water column. Continuing ocean acidification will have effects on CaCO3 and organic C metabolic responses to the oceanic inorganic C cycle, although those responses remain poorly quantified.  相似文献   

17.
Mangrove ecosystems play an important, but understudied, role in the cycling of carbon in tropical and subtropical coastal ocean environments. In the present study, we examined the diel dynamics of seawater carbon dioxide (CO2) and dissolved oxygen (DO) for a mangrove-dominated marine ecosystem (Mangrove Bay) and an adjacent intracoastal waterway (Ferry Reach) on the island of Bermuda. Spatial and temporal trends in seawater carbonate chemistry and associated variables were assessed from direct measurements of dissolved inorganic carbon, total alkalinity, dissolved oxygen (DO), temperature, and salinity. Diel pCO2 variability was interpolated across hourly wind speed measurements to determine variability in daily CO2 fluxes for the month of October 2007 in Bermuda. From these observations, we estimated rates of net sea to air CO2 exchange for these two coastal ecosystems at 59.8 ± 17.3 in Mangrove Bay and 5.5 ± 1.3 mmol m−2 d−1 in Ferry Reach. These results highlight the potential for large differences in carbonate system functioning and sea-air CO2 flux in adjacent coastal environments. In addition, observation of large diel variability in CO2 system parameters (e.g., mean pCO2: 390–2,841 μatm; mean pHT: 8.05–7.34) underscores the need for careful consideration of diel cycles in long-term sampling regimes and flux estimates.  相似文献   

18.
We measured monthly dissolved oxygen (DO) changes in situ benthic incubations from March 2001 to October 2002 in aPosidonia oceanica meadow and unvegetated sediments of Magalluf Bay (Mallorca Island, Spain) to determine gross primary production (GPP), community respiration (R), and net community production (NCP). From June 2001 to October 2002, we also measured fluxes of dissolved inorganic carbon (DIC) and total alkalinity (TAlk). The yearly integrated metabolic rates based on DO changes show that theP. oceanica communities are net autotrophic while the metabolic rates in the unvegetated benthic communities are nearly balanced. Higher calcium carbonate (CaCO3) cycling, both in terms of production and dissolution, was observed inP. oceanica communities than in unvegetated benthic communities. In theP. oceanica meadow, the annual release of CO2 from net CaCO3 production corresponds to almost half of the CO2 uptake by NCP based on DIC incubations. In unvegetated benthic communities, the annual uptake of CO2 from net CaCO3 dissolution almost fully compensates the CO2 release by NCP based on DIC incubations. CaCO3 dynamics is potentially a major factor in CO2 benthic fluxes in seagrass and carbonate-rich temperate coastal ecosystems.  相似文献   

19.
A reassessment of the abundance of dolomite in carbonate sediments has confirmed that carbonates deposited during the past 150 Ma contain, on average, less dolomite than Proterozoic and Paleozoic carbonates. The lower dolomite content of the more recent carbonate sediments results from the increase in the deposition of CaCO3 in deep-sea sediments, and to the difficulty of dolomitizing deep-sea CaCO3 by reaction with cold, unevaporated seawater. The decrease in the rate of dolomite formation during the past 150 Ma has led to an increase in the output of oceanic Mg+2 by the reaction of seawater with clay minerals and with ocean-floor basalts. The increase in the output of marine Mg+2 into these reservoirs has been brought about by an increase in the Mg+2 concentration of seawater. During the past 40 Ma, the concentration of Mg+2 in seawater has probably increased by ～18 mmol/kg, and probably has been accompanied by an equimolar increase in the concentration of SO4?2.  相似文献   

20.
《Applied Geochemistry》1995,10(4):461-475
The storage of CO2(liquid) on the seafloor has been proposed as a method of mitigating the accumulation of greenhouse gases in the Earth's atmosphere. Storage is possible below 3000 m water depth because the density of CO2(liquid) exceeds that of seawater and, thus, injected CO2(liquid) will remain as a stable, density stratified layer on the seafloor. The geochemical consequences of the storage of CO2(liquid) on the seafloor have been investigated using calculations of chemical equilibrium among complex aqueous solutions, gases, and minerals. At 3000 m water depth and 4°C, the stable phases are CO2(hydrate) and a brine. The hydrate composition is CO2·6.3H2O. The equilibrium composition of the brine is a 1.3 molal sodium-calcium-carbonate solution with pH ranging from 3.5 to 5.0. This acidified brine has a density of 1.04 g cm−3 and will displace normal seawater and react with underlying sediments. Seafloor sediment has an intrinsic capacity to neutralize the acid brine by dissolution of calcite and clay minerals and by incorporation of CO2 into carbonates including magnesite and dawsonite. Large volumes of acidified brine, however, can deplete the sediments buffer capacity, resulting in growth of additional CO2(hydrates) in the sediment. Volcanic sediments have the greatest buffer capacity whereas calcareous and siliceous oozes have the least capacity. The conditions that favor carbonate mineral stability and CO2(hydrates) stability are, in general, mutually exclusive although the two phases may coexist under restricted conditions.The brine is likely to cause mortality in both plant and animal comunities: it is acidic, it does not resemble seawater in composition, and it will have reduced capacity to hold oxygen because of the high solute content. Lack of oxygen will, consequently, produce anoxic conditions, however, the reduction of CO2 to CH4 is slow and redox disequilibrium mixtures of CO2 and CH4 are likely. Seismic or volcanic activity may cause conversion of CO2(liquid) to gas with potentially catastrophic release in a Lake Nyos-like event. The long term stability of the CO2(hydrate) may be limited: once isolated from the CO2(liquid) pool, either through burial or through depletion of the CO2 pool, the hydrate will decopose, releasing CO2 back into the sediment-water system.  相似文献   

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