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1.
El Chichón crater lake appeared immediately after the 1982 catastrophic eruption in a newly formed, 1-km wide, explosive crater. During the first 2 years after the eruption the lake transformed from hot and ultra-acidic caused by dissolution of magmatic gases, to a warm and less acidic lake due to a rapid “magmatic-to-hydrothermal transition” — input of hydrothermal fluids and oxidation of H2S to sulfate. Chemical composition of the lake water and other thermal fluids discharging in the crater, stable isotope composition (δD and δ18O) of lake water, gas condensates and thermal waters collected in 1995–2006 were used for the mass-balance calculations (Cl, SO4 and isotopic composition) of the thermal flux from the crater floor. The calculated fluxes of thermal fluid by different mass-balance approaches become of the same order of magnitude as those derived from the energy-budget model if values of 1.9 and 2 mmol/mol are taken for the catchment coefficient and the average H2S concentration in the hydrothermal vapors, respectively. The total heat power from the crater is estimated to be between 35 and 60 MW and the CO2 flux is not higher than 150 t/day or ~ 200 gm− 2 day− 1.  相似文献   

2.
We observed a phytoplankton bloom downstream of a large estuarine plume induced by heavy precipitation during a cruise conducted in the Pearl River estuary and the northern South China Sea in May–June 2001. The plume delivered a significant amount of nutrients into the estuary and the adjacent coastal region, and enhanced stratification stimulating a phytoplankton bloom in the region near and offshore of Hong Kong. A several fold increase (0.2–1.8 μg Chl L−1) in biomass (Chl a) was observed during the bloom. During the bloom event, the surface water phytoplankton community structure significantly shifted from a pico-phytoplankton dominated community to one dominated by micro-phytoplankton (>20 μm). In addition to increased Chl a, we observed a significant drawdown of pCO2, biological uptake of dissolved inorganic carbon (DIC) and an associated enhancement of dissolved oxygen and pH, demonstrating enhanced photosynthesis during the bloom. During the bloom, we estimated a net DIC drawdown of 100–150 μmol kg−1 and a TAlk increase of 0–50 μmol kg−1. The mean sea–air CO2 flux at the peak of the bloom was estimated to be as high as ∼−18 mmol m−2 d−1. For an average surface water depth of 5 m, a very high apparent biological CO2 consumption rate of 70–110 mmol m−2 d−1 was estimated. This value is 2–6 times higher than the estimated air–sea exchange rate.  相似文献   

3.
Na–HCO3–CO2-rich thermomineral waters issue in the N of Portugal, within the Galicia-Trás-os-Montes region, linked to a major NNE-trending fault, the so-called Penacova-Régua-Verin megalineament. Along this tectonic structure different occurrences of CO2-rich thermomineral waters are found: Chaves hot waters (67 °C) and also several cold (16.1 °C) CO2-rich waters. The δ2H and δ18O values of the thermomineral waters are similar to those of the local meteoric waters. The chemical composition of both hot and cold mineral waters suggests that water–rock reactions are mainly controlled by the amount of dissolved CO2 (g) rather than by the water temperature. Stable carbon isotope data indicate an external CO2 inorganic origin for the gas. δ13CCO2 values ranging between ? 7.2‰ and ? 5.1‰ are consistent with a two-component mixture between crustal and mantle-derived CO2. Such an assumption is supported by the 3He/4He ratios measured in the gas phase, are between 0.89 and 2.68 times the atmospheric ratio (Ra). These ratios which are higher than that those expected for a pure crustal origin (≈ 0.02 Ra), indicating that 10 to 30% of the He has originated from the upper mantle. Release of deep-seated fluids having a mantle-derived component in a region without recent volcanic activity indicates that extensive neo-tectonic structures originating during the Alpine Orogeny are still active (i.e., the Chaves Depression).  相似文献   

4.
The air–sea ice CO2 flux was measured over landfast sea ice in the Chukchi Sea, off Barrow, Alaska in late May 2008 with a chamber technique. The ice cover transitioned from a cold early spring to a warm late spring state, with an increase in air temperature and incipient surface melt. During melt, brine salinity and brine dissolved inorganic carbon concentration (DIC) decreased from 67.3 to 18.7 and 3977.6 to 1163.5 μmol kg−1, respectively. In contrast, the salinity and DIC of under-ice water at depths of 3 and 5 m below the ice surface remained almost constant with average values of 32.4±0.3 (standard deviation) and 2163.1±16.8 μmol kg−1, respectively. The air–sea ice CO2 flux decreased from +0.7 to −1.0 mmol m−2 day−1 (where a positive value indicates CO2 being released to the atmosphere from the ice surface). During this early to late spring transition, brought on by surface melt, sea ice shifted from a source to a sink for atmospheric CO2, with a rapid decrease of brine DIC likely associated with a decrease in the partial pressure of CO2 of brine from a supersaturated to an undersaturated state compared to the atmosphere. Formation of superimposed ice coincident with melt was not sufficient to shut down ice–air gas exchange.  相似文献   

5.
In the summer of 2005, continuous surface water measurements of fugacity of CO2 (fCO2sw), salinity and temperature were performed onboard the IB Oden along the Northwest Passage from Cape Farwell (South Greenland) to the Chukchi Sea. The aim was to investigate the importance of sea ice and river runoff on the spatial variability of fCO2 and the sea–air CO2 fluxes in the Arctic Ocean. Additional data was obtained from measurements of total alkalinity (AT) by discrete surface water and water column sampling in the Canadian Arctic Archipelago (CAA), on the Mackenzie shelf, and in the Bering Strait. The linear relationship between AT and salinity was used to evaluate and calculate the relative fractions of sea ice melt water and river runoff along the cruise track. High-frequency fCO2sw data showed rapid changes, due to variable sea ice conditions, freshwater addition, physical upwelling and biological processes. The fCO2sw varied between 102 and 678 μatm. Under the sea ice in the CAA and the northern Chukchi Sea, fCO2sw were largely CO2 undersaturated of approximately 100 μatm lower than the atmospheric level. This suggested CO2 uptake by biological production and limited sea–air CO2 gas exchange due to the ice cover. In open areas, such as the relatively fresh water of the Mackenzie shelf and the Bering Strait, the fCO2sw values were close to the atmospheric CO2 level. Upwelling of saline and relatively warm water at the Cape Bathurst caused a dramatic fCO2sw increase of about 100 μatm relative to the values in the CAA. At the southern part of the Chukchi Peninsula we found the highest fCO2sw values and the water was CO2 supersaturated, likely due to upwelling. In the study area, the calculated sea–air CO2 flux varied between an oceanic CO2 sink of 140 mmol m−2 d−1 and an oceanic source of 18 mmol m−2 d−1. However, in the CAA and the northern Chukchi Sea, the sea ice cover prevented gas exchange, and the CO2 fluxes were probably negligible at this time of the year. Assuming that the water was exposed to the atmosphere by total melting and gas exchange would be the only process, the CO2 undersaturated water in the ice-covered areas will not have the time to reach the atmospheric CO2 value, before the formation of new sea ice. This study highlights the value of using high-frequency measurements to gain increased insight into the variable and complex conditions, encountered on the shelves in the Arctic Ocean.  相似文献   

6.
The Miocene Tejeda caldera on Gran Canaria erupted ~ 20 rhyolite–trachyte ignimbrites (Mogán Group 14–13.3 Ma), followed by ~ 20 phonolitic lava flows and ignimbrites (Fataga Group 13–8.5 Ma). Upper-Mogán tuffs have been severely altered immediately within the caldera margin, whereas extra-caldera Mogán ignimbrites, and overlying Fataga units, are apparently unaltered. The altered intra-caldera samples contain minerals characteristic of secondary fluid–rock interaction (clays, zeolites, adularia), and relics of the primary mineral assemblage identified in unaltered ignimbrites (K-feldspar, plagioclase, pyroxene, amphibole, and groundmass quartz). Major and trace-element data indicate that Si, Na, K, Pb, Sr, and Rb, were strongly mobilized during fluid–rock interaction, whereas Ti, Zr, and Nb behaved in a more refractory manner, experiencing only minor mobilization. The δ18O values of the altered intra-caldera tuffs are significantly higher than in unaltered extra-caldera ignimbrites, consistent with an overall low-temperature alteration environment. Unaltered extra-caldera ignimbrites have δD values between − 110‰ and − 173‰, which may reflect Rayleigh-type magma degassing and/or post-depositional vapour release. The δD values of the altered intra-caldera tuffs range from − 52‰ to − 131‰, with ambient meteoric water at the alteration site estimated at ca. − 15‰. Interaction and equilibration of the intra-caldera tuffs with ambient meteoric water at low temperature can only account for whole-rock δD values of around − 45‰, given that ?Dclay–water is ca. − 30‰ at 100 °C, and decreases in magnitude at higher temperatures. All altered tuff samples have δD values that are substantially lower than − 45‰, indicating interaction with a meteoric water source with a δD value more negative than − 15‰, which may have been produced in low-temperature steam fumaroles. Supported by numerical modeling, our Gran Canaria data reflect the near-surface, epithermal part of a larger, fault-controlled hydrothermal system associated with the emplacement of the high-level Fataga magma chamber system. In this near-surface environment, fluid temperatures probably did not exceed 200–250 °C.  相似文献   

7.
The Yangyi geothermal field, located 72 km northwest to Lhasa City, capital of Tibet, has a high reservoir temperature up to at least 207.2 °C. The geothermal waters from both geothermal wells and hot springs belong to the HCO3 (+CO3)–Na type. Factor analysis of all the chemical constituents shows that they can be divided into two factors: F1 factor receives the contributions of SO42−, Cl−, SiO2, As, B, Na+, K+, and Li+; whereas F2 factor is explained by HCO3−, F−, CO32−, Ca2+, and Sr2+. The F1 factor can be regarded as an indicator of the reservoir temperature distribution at Yangyi, but its variable correlation with the results of different geothermometers (Na–K, quartz and K–Mg) does not allow one to draw further inferences. Different from F1, the F2 factor is an indicator of a group of hydrogeochemical processes resulting from the CO2 pressure decrease in geothermal water during its ascent from the deep underground, including transformation of HCO3− to CO32−, precipitation of Ca2+ and Sr2+, and release of F− from some fluoride-bearing minerals of reservoir rocks. The plot of enthalpy vs. chloride, prepared on the basis of Na–K equilibrium temperatures, suggests that a parent geothermal liquid (PGL) with Cl− concentration of 185 mg/L (that of sample YYT-8) and enthalpy of 1020 J/g (corresponding to a temperature of 236–237 °C, i.e., somewhat higher than that of sample YYT-6) is present in the geothermal reservoir of the Yangyi area, below both the Qialagai valley and the Bujiemu valley, although the samples less affected by mixing and cooling (YYT-6 and YYT-7) come from the second site. The discharge of geothermal waters with high contents of toxic elements such as B, As and F into the Luolang River, the only drinking water source for local residents, has caused slight pollution of the river water. Great care should therefore be taken in the geothermal water resource management at Yangyi.  相似文献   

8.
The southern Yellow Sea (SYS), located to the north of the East China Sea (ECS), was considered part of the ECS when Tsunogai et al. (1999) proposed the “continental shelf pump” (CSP) hypothesis. However, the original CSP carbon dioxide (CO2) uptake flux (2.9 mol C m−2 yr−1) appears to have been overestimated, primarily due to the differences between the SYS and the ECS in terms of their CO2 system. In this paper, we estimated air-sea CO2 fluxes in the SYS using the surface water partial pressure of CO2 (pCO2) measured in winter, spring, and summer, as well as that estimated in fall via the relationship of pCO2 with salinity, temperature, and chlorophyll a. The results indicate that overall, the entire investigated area was a net source of atmospheric CO2 during summer, winter, and fall, whereas it was a net sink during spring. Spatially, the nearshore area was almost a permanent CO2 source, while the central SYS shifted from being a CO2 sink in spring to a source in the other seasons of the year. Overall, the SYS is a net source of atmospheric CO2 on an annual scale, releasing ∼7.38 Tg C (1 Tg=1012 g) to the atmosphere annually. Thus, the updated CO2 uptake flux in the combined SYS and ECS is reduced to ∼0.86 mol C m−2 yr−1. If this value is extrapolated globally following Tsunogai et al. (1999), the global continental shelf would be a sink of ∼0.29 Pg C yr−1, instead of 1 Pg C yr−1 (1 Pg=1015 g).The SYS as a net annual source of atmospheric CO2 is in sharp contrast to most mid- and high-latitude continental shelves, which are CO2 sinks. We argue that unlike the ECS and the North Sea where carbon on the shelf could be exported to the open ocean, the SYS lacks the physical conditions required by the CSP to transport carbon off the shelf effectively. The global validity of the CSP theory is thus questionable.  相似文献   

9.
We estimated the net annual air–sea exchange of carbon dioxide (CO2) using monitoring data from the East Gotland Sea, Bornholm Sea, and Kattegat for the 1993–2009 period. Wind speed and the sea surface partial pressure of CO2 (pCO2w), calculated from pH, total alkalinity, temperature, and salinity, were used for the flux calculations. We demonstrate that regions in the central Baltic Sea and the Kattegat alternate between being sinks (−) and sources (+) of CO2 within the −4.2 to +5.2 mol m−2 yr−1 range. On average, for the 1994–2008 period, the East Gotland Sea was a source of CO2 (1.64 mol m−2 yr−1), the Bornholm Sea was a source (2.34 mol m−2 yr−1), and the Kattegat was a sink (−1.16 mol m−2 yr−1). Large inter-annual and regional variations in the air–sea balance were observed. We used two parameterizations for the gas transfer velocity (k) and the choice varied the air–sea exchange by a factor of two. Inter-annual variations in pCO2w between summers were controlled by the maximum concentration of phosphate in winter. Inter-annual variations in the CO2 flux and gas transfer velocity were larger between winters than between summers. This indicates that the inter-annual variability in the total flux was controlled by winter conditions. The large differences between the central Baltic Sea and Kattegat were considered to depend partly on the differences in the mixed layer depth.  相似文献   

10.
The Alban Hills volcanic region (20 km south of Rome, in the Roman Province) emitted a large volume of potassic magmas (> 280 km3) during the Quaternary. Chemical interactions between ascending magmas and the ∼ 7000–8000-m-thick sedimentary carbonate basement are documented by abundant high temperature skarn xenoliths in the eruptive products and have been frequently corroborated by geochemical surveys. In this paper we characterize the effect of carbonate assimilation on phase relationships at 200 MPa and 1150–1050 °C by experimental petrology. Calcite and dolomite addition promotes the crystallization of Ca-rich pyroxene and Mg-rich olivine respectively, and addition of both carbonates results in the desilication of the melt. Furthermore, carbonate assimilation liberates a large quantity of CO2-rich fluid. A comparison of experimental versus natural mineral, glass and bulk rock compositions suggests large variations in the degree of carbonate assimilation for the different Alban Hills eruptions. A maximum of 15 wt.% assimilation is suggested by some melt inclusion and clinopyroxene compositions; however, most of the natural data indicate assimilation of between 3 and 12 wt.% carbonate. Current high CO2 emissions in this area most likely indicate that such an assimilation process still occurs at depth. We calculate that a magma intruding into the carbonate basement with a rate of ∼ 1 – 2 · 106 m3/year, estimated by geophysical studies, and assimilating 3–12 wt.% of host rocks would release an amount of CO2 matching the current yearly emissions at the Alban Hills. Our results strongly suggest that current CO2 emissions in this region are the shallow manifestation of hot mafic magma intrusion in the carbonate-hosted reservoir at 5–6 km depth, with important consequences for the present-day volcanic hazard evaluation in this densely populated and historical area.  相似文献   

11.
Our understanding of the ancient ocean-atmosphere system has focused on oceanic proxies. However, the study of terrestrial proxies is equally necessary to constrain our understanding of ancient climates and linkages between the terrestrial and oceanic carbon reservoirs. We have analyzed carbon-isotope ratios from fossil plant material through the Valanginian and Lower Hauterivian from a shallow-marine, ammonite-constrained succession in the Crimean Peninsula of the southern Ukraine in order to determine if the Upper Valanginian positive carbon-isotope excursion is expressed in the atmosphere. δ13Cplant values fluctuate around − 23‰ to − 22‰ for the Valanginian-Hauterivian, except during the Upper Valanginian where δ13Cplant values record a positive excursion to ∼− 18‰. Based upon ammonite biostratigraphy from Crimea, and in conjunction with a composite Tethyan marine δ13Ccarb curve, several conclusions can be drawn: (1) the δ13Cplant record indicates that the atmospheric carbon reservoir was affected; (2) the defined ammonite correlations between Europe and Crimea are synchronous; and (3) a change in photosynthetic carbon-isotope fractionation, caused by a decrease in atmospheric pCO2, occurred during the Upper Valanginian positive δ13C excursion. Our new data, combined with other paleoenvironmental and paleoclimatic information, indicate that the Upper Valanginian was a cool period (icehouse) and highlights that the Cretaceous period was interrupted by periods of cooling and was not an equable climate as previously thought.  相似文献   

12.
The 3-d coupled physical–biogeochemical model ECOHAM (version 3) was applied to the Northwest-European Shelf (47°41′–63°53′N, 15°5′W–13°55′E) for the years 1993–1996. Carbon fluxes were calculated for the years 1995 and 1996 for the inner shelf region, the North Sea (511,725 km2). This period was chosen because it corresponds to a shift from a very high winter-time North Atlantic Oscillation Index (NAOI) in 1994/1995, to an extremely low one in 1995/1996, with consequences for the North Sea physics and biogeochemistry. During the first half of 1996, the observed mean SST was about 1 °C lower than in 1995; in the southern part of the North Sea the difference was even larger (up to 3 °C). Due to a different wind regime, the normally prevailing anti-clockwise circulation, as found in winter 1995, was replaced by more complicated circulation patterns in winter 1996. Decreased precipitation over the drainage area of the continental rivers led to a reduction in the total (inorganic and organic) riverine carbon load to the North Sea from 476 Gmol C yr−1 in 1995 to 340 Gmol C yr−1 in 1996. In addition, the North Sea took up 503 Gmol C yr−1 of CO2 from the atmosphere. According to our calculations, the North Sea was a sink for atmospheric CO2, at a rate of 0.98 mol C m−2 yr−1, for both years. The North Sea is divided into two sub-systems: the shallow southern North Sea (SNS; 190,765 km2) and the deeper northern North Sea (NNS; 320,960 km2). According to our findings the SNS is a net-autotrophic system (net ecosystem production NEP>0) but released CO2 to the atmosphere: 159 Gmol C yr−1 in 1995 and 59 Gmol C yr−1 in 1996. There, the temperature-driven release of CO2 outcompetes the biological CO2 drawdown. In the NNS, where respiratory processes prevail (NEP<0), 662 and 562 Gmol C yr−1 were taken up from the atmosphere in 1995 and 1996, respectively. Stratification separates the productive, upper layer from the deeper layers of the water column where respiration/remineralization takes place. Duration and stability of the stratification are determined by the meteorological conditions, in relation to the NAO. Our results suggest that this mechanism controlling the nutrient supply to the upper layer in the northern and central North Sea has a larger impact on the carbon fluxes than changes in lateral transport due to NAOI variations. The North Sea as a whole imports organic carbon and exports inorganic carbon across the outer boundaries, and was found to be net-heterotrophic, more markedly in 1996 than in 1995.  相似文献   

13.
Gas emissions from Tatun volcanic group, northern Taiwan, were studied for the first time using a multi-component gas analyser system (Multi-GAS) in combination with Giggenbach flask methods at fumaroles and mud pools at Da-you-keng (DYK) and Geng-tze-ping (GZP). CO2/S molar ratios observed at DYK ranged from 3–17, similar ratios were observed using a Multi-GAS sensor box of 8–16. SO2 at GZP was low, higher concentrations were observed at DYK where SO2/H2S ratios were close to 1 for both methods. A lower CO2/H2S ratio was measured via Giggenbach flask sampling (7.2) than was found in the plume using the gas sensor at GZP (9.2). This may reflect rapid oxidation of H2S as it mixes with background air. Gaseous elemental mercury (GEM) levels were observed in the fumarole gases using a portable mercury spectrometer. These are the first such measurements of mercury at Tatun. Mean GEM concentrations in the fumarole plumes were ∼ 20 ng m− 3, with much higher concentrations observed close to the ground (mean [GEM] 130 and 290 ng m− 3 at DYK and GZP, respectively). The GEM in the fumarole plume was elevated above concentrations in industrial/urban air in northern Taiwan and the increase in GEM observed when the instrument was lowered suggests high levels of mercury are present in the surrounding ground surface. The GEM/CO2 (10− 8) and GEM/S (10− 6) ratios observed in the fumarole gases were comparable to those observed at other low-temperature fumaroles. Combining the Hg/CO2 ratio with a previous CO2 flux value for the area, the annual GEM flux from the Tatun field is estimated as 5–50 kg/year.  相似文献   

14.
Cruises to Bering Strait and the Chukchi Sea in US waters from late June in 2002 to early September in 2004 and the Russian–American Long-term Census of the Arctic (RUSALCA) research cruise in 2004 covered all major water masses and contributed to a better understanding of the regional physics, nutrient dynamics, and biological systems. The integrated concentration of the high nitrate pool in the central Chukchi Sea was greater in this study than in previous studies, although the highest nitrate concentration (∼22 μM) in the Anadyr Water mass passing through the western side of Bering Strait was consistent with prior observations. The chlorophyll-a concentrations near the western side of the Diomede Islands ranged from 200 to 400 mg chl-a m−2 and the range in the central Chukchi Sea was 200–500 mg chl-a m−2 for the 2002–2004 Alpha Helix (HX) cruises. Chlorophyll-a concentrations for the 2004 RUSALCA cruise were lower than those from previous studies. The mean annual primary production of phytoplankton from this study, using a 13C–15N dual-isotope technique, was 55 g C m−2 for the whole Chukchi Sea and 145 g C m−2 for the plume of Anadyr–Bering Shelf Water in the central Chukchi Sea. In contrast, the averages of annual total nitrogen production were 13.9 g N m−2 (S.D.=±16.2 g N m−2) and 33.8 g N m−2 (S.D.=±14.1 g N m−2) for the Chukchi Sea and the plume, respectively. These carbon and nitrogen production rates of phytoplankton were consistently two-or three-fold lower than those from previous studies. We suggest that the lower rates in this study, and consequently more unused nitrate in the water column, were caused by lower phytoplankton biomass in the Bering Strait and the Chukchi Sea. However, we do not know if the lower rate of production from this study is a general decreasing trend or simply temporal variations in the Chukchi Sea, since temporal and geographical variations are substantially large and presently unpredictable.  相似文献   

15.
Coastal upwelling events in the California Current System can transport subsurface waters with high levels of carbon dioxide (CO2) to the sea surface near shore. As these waters age and are advected offshore, CO2 levels decrease dramatically, falling well below the atmospheric concentration beyond the continental shelf break. In May 2007 we observed an upwelling event off the coast of northern California. During the upwelling event subsurface respiration along the upwelling path added ∼35 μmol kg−1 of dissolved inorganic carbon (DIC) to the water as it transited toward shore causing the waters to become undersaturated with respect to Aragonite. Within the mixed layer, pCO2 levels were reduced by the biological uptake of DIC (up to 70%), gas exchange (up to 44%), and the addition of total alkalinity through CaCO3 dissolution in the undersaturated waters (up to 23%). The percentage contribution of each of these processes was dependent on distance from shore. At the time of measurement, a phytoplankton bloom was just beginning to develop over the continental shelf. A box model was used to project the evolution of the water chemistry as the bloom developed. The biological utilization of available nitrate resulted in a DIC decrease of ∼200 μmol kg−1, sea surface pCO2 near ∼200 ppm, and an aragonite saturation state of ∼3. These results suggest that respiration processes along the upwelling path generally increase the acidification of the waters that are being upwelled, but once the waters reach the surface biological productivity and gas exchange reduce that acidification over time.  相似文献   

16.
Partial pressure of CO2 in equilibrium with sample water (pCO2) for the coastal water in the Chukchi Sea was continuously observed in summer, 2008. Average daily CO2 flux calculated from the pCO2 and gas transfer coefficients ranged from −0.144 to −0.0701 g C m−2 day−1 depending on which gas transfer coefficient was used. The pCO2 before the landfast ice sheets melted appeared to be highly biologically controlled based on the following information: (1) the diurnal pattern of pCO2 was strongly correlated with Photosynthetic Photon Flux Density (PPFD); (2) high chlorophyll density was observed during periods of peak uptake; and (3) the day-to-day variation in the pCO2 strongly correlated with the presence or absence of near-shore ice sheets. The lowest pCO2 of 35 ppm together with the highest PPFD of 1362 μmol E m−2 s−1 were observed in the afternoon on June 28 in the presence of sea ice. The very low pCO2 observed in late June was likely caused by high photosynthetic rates related to high phytoplankton densities typically observed from spring to early summer near the ice edge, and by water low in salinity and CO2 released by melting sea ice early in the season.  相似文献   

17.
Mount Erebus, Antarctica, is a large (3794 m) alkaline open-conduit stratovolcano that hosts a vigorously convecting and persistently degassing lake of anorthoclase phonolite magma. The composition of the lake was investigated by analyzing glass and mineral compositions in lava bombs erupted between 1972 and 2004. Matrix glass, titanomagnetite, olivine, clinopyroxene, and fluor-apatite compositions are invariant and show that the magmatic temperature (∼ 1000°C) and oxygen fugacity (ΔlogFMQ = − 0.9) have been stable. Large temperature variations at the lake surface (~ 400–500°C) are not reflected in mineral compositions. Anorthoclase phenocrysts up to 10 cm in length feature a restricted compositional range (An10.3–22.9Ab62.8–68.1Or11.4–27.2) with complex textural and compositional zoning. Anorthoclase textures and compositions indicate crystallization occurs at low degrees of effective undercooling. We propose shallow water exsolution causes crystallization and shallow convection cycles the anorthoclase crystals through many episodes of growth resulting in their exceptional size. Minor variations in eruptive activity from 1972 to 2004 are decoupled from magma compositions. The variations probably relate to changes in conduit geometry within the volcano and/or variable input of CO2-rich volatiles into the upper-level magma chamber from deeper in the system.  相似文献   

18.
Saronikos Gulf (Greece) practically constitutes the sea border of the metropolitan city of Athens and the alongshore outskirts, and it receives the treated wastes of ∼4 million people from a point source that discharges on the sea bottom at ∼65 m water depth. Total organic carbon (TOC) was measured in 477 seawater samples collected in the Saronikos Gulf, during 10 cruises, from August 2001 to May 2004 and analyzed with the High Temperature Catalytic Oxidation method (HTCO). TOC concentrations ranged from 49 to 198 μmol C L−1 in agreement with other Mediterranean coastal waters. The highest TOC concentrations were found in the upper waters (0–75 m), whereas in the deeper parts of the Gulf (between 100 and 400 m) TOC concentrations were kept constantly low (49–70 μmol C L−1). A general pattern towards higher TOC concentrations during summer was also observed. Calculations of non-refractory (labile+semi-labile) organic material based on a one-dimensional (1D) conceptual model showed that it corresponds to 33% of the bulk TOC during summer and to 27% during winter. Bacterial production (BP) was measured at selected stations of ∼70–80 m depth using the [3H] leucine method. Depth integrated BP values varied from 2.8 to 10.9 mmol m−2 d−1, whereas extraordinary high integrated BP values (126 and 140 mmol m−2 d−1) were observed at the station over the treated sewage outflow. From the turnover time, τ, of the non-refractory TOC by bacteria it was implied that organic matter in the effluents is extremely labile (2–58 days). Moreover, τ values at the other sites showed that during summer non-refractory organic material resisted bacterial degradation (1–8 months), whereas during early spring it was easily degradable (20–50 days). The balance of TOC fluxes for the Inner Gulf for June and September 2003 showed that the Inner Gulf acts as a net producer of TOC during summer. Our results suggest that the presence of the Athens treated sewage outfall does not contribute to the observed summer accumulation of TOC in the Inner Gulf and other causes such as increased bacteria predation and/or nutrient limitation must be responsible.  相似文献   

19.
The biogeochemistry of methane in the sediments of Lake Caviahue was examined by geochemical analysis, microbial activity assays and isotopic analysis. The pH in the water column was 2.6 and increased up to a pH of 6 in the deeper sediment pore waters. The carbon isotope composition of CH4 was between − 65 and − 70‰ which is indicative for the biological origin of the methane. The enrichment factor ε increased from − 46‰ in the upper sediment column to more than − 80 in the deeper sediment section suggesting a transition from acetoclastic methanogenesis to CO2 reduction with depth. In the most acidic surface layer of the sediment (pH < 4) methanogenesis is inhibited as suggested by a linear CH4 concentration profile, activity assays and MPN analysis. The CH4 activity assays and the CH4 profile indicate that methanogenesis in the sediment of Lake Caviahue was active below 40 cm depth. At that depth the pH was above 4 and sulfate reduction was sulfate limited. Methane was diffusing with a flux of 0.9 mmol m− 2 d− 1 to the sediment surface where it was probably oxidized. Methanogenesis contributed little to the sediments carbon budget and had no significant impact on lake water quality. The high biomass content of the sediment, which was probably caused by the last eruption of Copahue Volcano, supported high rates of sulfate reduction which probably raised the pH and created favorable conditions for methanogens in deeper sediment layers.  相似文献   

20.
We characterize and quantify volatile emissions at Hot Spring Basin (HSB), a large acid-sulfate region that lies just outside the northeastern edge of the 640 ka Yellowstone Caldera. Relative to other thermal areas in Yellowstone, HSB gases are rich in He and H2, and mildly enriched in CH4 and H2S. Gas compositions are consistent with boiling directly off a deep geothermal liquid at depth as it migrates toward the surface. This fluid, and the gases evolved from it, carries geochemical signatures of magmatic volatiles and water–rock reactions with multiple crustal sources, including limestones or quartz-rich sediments with low K/U (or 40?Ar/4?He). Variations in gas chemistry across the region reflect reservoir heterogeneity and variable degrees of boiling. Gas-geothermometer temperatures approach 300 °C and suggest that the reservoir feeding HSB is one of the hottest at Yellowstone. Diffuse CO2 flux in the western basin of HSB, as measured by accumulation-chamber methods, is similar in magnitude to other acid-sulfate areas of Yellowstone and is well correlated to shallow soil temperatures. The extrapolation of diffuse CO2 fluxes across all the thermal/altered area suggests that 410 ± 140 t d− 1 CO2 are emitted at HSB (vent emissions not included). Diffuse fluxes of H2S were measured in Yellowstone for the first time and likely exceed 2.4 t d− 1 at HSB. Comparing estimates of the total estimated diffuse H2S emission to the amount of sulfur as SO42− in streams indicates ~ 50% of the original H2S in the gas emission is lost into shallow groundwater, precipitated as native sulfur, or vented through fumaroles. We estimate the heat output of HSB as ~ 140–370 MW using CO2 as a tracer for steam condensate, but not including the contribution from fumaroles and hydrothermal vents. Overall, the diffuse heat and volatile fluxes of HSB are as great as some active volcanoes, but they are a small fraction (1–3% for CO2, 2–8% for heat) of that estimated for the entire Yellowstone system.  相似文献   

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