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1.
We used clear, acrylic chambers to measure in situ community oxygen and nutrient fluxes under day and night conditions in seagrass beds at five sites across Florida Bay five times between September 1997 and March 1999. Underlying sediments are biogenic carbonate with porosities of 0.7–0.9 and with low organic content (<1.6%). The seagrass communities always removed oxygen from the water column during the night and produced oxygen during daylight, and sampling date and site significantly affected both night and daytime oxygen fluxes. Net daily average fluxes of oxygen (?4.9 to 49 mmol m?2 day?1) ranged from net autotrophy to heterotrophy across the bay and during the 18-month sampling period. However, the Rabbit Key Basin site, located in the west-central bay and covered with a dense Thalassia testudinum bed, was always autotrophic with net average oxygen production ranging from 4.8 to 49 mmol m?2 day?1. In November 1998, three of the five sites were strongly heterotrophic and oxygen production was least at Rabbit, suggesting the possibility of hypoxic conditions in fall. Average ammonium (NH4) concentrations in the water column varied widely across the bay, ranging from a mean of 6.9 μmol l?1 at Calusa in the eastern bay to a mean of 0.6 μmol l?1 at Rabbit Key for the period of study. However, average NH4 fluxes by site and date (?240 to 110 μmol m?2 h?1) were not correlated with water column concentrations and did not vary in a consistent diel, seasonal, or spatial pattern. Concentrations of dissolved organic nitrogen (DON) in the water column, averaged by site (15–25 μmol l?1), were greater than mean NH4 concentrations, and the range of day and night DON fluxes (?920 to 1,300 μmol m?2 h?1), averaged by site and date, was greater than the range of mean NH4 fluxes. Average DON fluxes did not vary consistently from day to night, seasonally or spatially. Mean silicate fluxes ranged from ?590 to 860 μmol m?2 h?1 across all sites and dates, but mean net daily fluxes were less variable and most of the time contributed small amounts of silicate to the water column. Mean concentrations of filterable reactive phosphorus (FRP) in the water column across the bay were very low (0.021–0.075 μmol l?1); but site average concentrations of dissolved organic phosphorus (DOP) were higher (0.04–0.15 μmol l?1) and showed a gradient of increasing concentration from east to west in the bay. A pronounced gradient in average surficial sediment total phosphorus (1.1–12 μmol g DW?1) along an east-to-west gradient was not reflected in fluxes of phosphorus. FRP fluxes, averaged by site and date, were low (?5.2 to 52 μmol m?2 h?1), highly variable, and did not vary consistently from day to night or across season or location. Mean DOP fluxes varied over a smaller range (?8.7 to 7.4 μmol m?2 h?1), but also showed no consistent spatial or temporal patterns. These small DOP fluxes were in sharp contrast to the predominately organic phosphorus pool in surficial sediments (site means?=?0.66–7.4 μmol g DW?1). Significant correlations of nutrient fluxes with parameters related to seagrass abundance suggest that the seagrass community may play a major role in nutrient recycling. Integrated means of net daily fluxes over the area of Florida Bay, though highly variable, suggest that seagrass communities might be a source of DOP and NH4 to Florida Bay and might remove small amounts of FRP and potentially large amounts of DON from the waters of the bay. 相似文献
2.
Sediment-water oxygen and nutrient (NH4 +, NO3 ?+NO2 ?, DON, PO4 3?, and DSi) fluxes were measured in three distinct regions of Chesapeake Bay at monthly intervals during 1 yr and for portions of several additional years. Examination of these data revealed strong spatial and temporal patterns. Most fluxes were greatest in the central bay (station MB), moderate in the high salinity lower bay (station SB) and reduced in the oligohaline upper bay (station NB). Sediment oxygen consumption (SOC) rates generally increased with increasing temperature until bottom water concentrations of dissolved oxygen (DO) fell below 2.5 mg l?1, apparently limiting SOC rates. Fluxes of NH4 + were elevated at temperatures >15°C and, when coupled with low bottom water DO concentrations (<5 mg l?1), very large releases (>500 μmol N m?2 h?1) were observed. Nitrate + nitrite (NO3 ?+NO2 ?) exchanges were directed into sediments in areas where bottom water NO3 ?+NO2 ? concentrations were high (>18 μM N); sediment efflux of NO3 ?+NO2 ? occurred only in areas where bottom water NO3 ?+NO2 ? concentrations were relatively low (<11 μM N) and bottom waters well oxygenated. Phosphate fluxes were small except in areas of hypoxic and anoxic bottom waters; in those cases releases were high (50–150 μmol P m?2 h?1) but of short duration (2 mo). Dissolved silicate (DSi) fluxes were directed out of the sediments at all stations and appeared to be proportional to primary production in overlying waters. Dissolved organic nitrogen (DON) was released from the sediments at stations NB and SB and taken up by the sediments at station MB in summer months; DON fluxes were either small or noninterpretable during cooler months of the year. It appears that the amount and quality of organic matter reaching the sediments is of primary importance in determining the spatial variability and interannual differences in sediment nutrient fluxes along the axis of the bay. Surficial sediment chlorophyll-a, used as an indicator of labile sediment organic matter, was highly correlated with NH4 ?, PO4 3?, and DSi fluxes but only after a temporal lag of about 1 mo was added between deposition events and sediment nutrient releases. Sediment O:N flux ratios indicated that substantial sediment nitrification-denitrification probably occurred at all sites during winter-spring but not summer-fall; N:P flux ratios were high in spring but much less than expected during summer, particularly at hypoxic and anoxic sites. Finally, a comparison of seasonal N and P demand by phytoplankton with sediment nutrient releases indicated that the sediments provide a substantial fraction of nutrients required by phytoplankton in summer, but not winter, especially in the mid bay region. 相似文献
3.
The rate of zooplankton ammonium regeneration was measured in Great South Bay, Long Island, New York, between July 1982 and May 1984. Ammonium excretion by macrozooplankton (>200 μm) ranged from 7 μg atoms NH4 1+?N m?3 d?1 in winter to 156 μg-atoms NH4 1+?N m?3 d?1 in spring. Ammonium excretion by ctenophores was greater than or equivalent to that of macrozooplankton during the period of ctenophore biomass maximum in summer and fall. The temperature coefficient (Q10) for NH4 1+ excretion was 1.74 from 2.2 to 27.5°C for macrozooplankton and 1.63 between 17 and 26°C for the ctenophores. Ammonium nitrogen excretion by macrozooplankton and ctenophores combined, accounted for 1 to 3% of phytoplankton nitrogen requirements in summer when primary productivity was high and 39% in the spring. *** DIRECT SUPPORT *** A01BY040 00005 相似文献
4.
Transport of ammonium (NH4 +), nitrate + nitrite (NO3 ?), total Kjeldahl nitrogen (TKN), soluble reactive phosphate (SRP), and total suspended solids (TSS) was measured in a freshwater tidal bayou located in a marsh system near the mouth of the Atchafalaya River in Louisiana. Sampling was conducted six times over one year and was timed to assess effects of seasonal variation in river flow and mean sea level of the Gulf of Mexico on material fluxes. Net fluxes of all materials were large and ebb directed in all seasons except fall, when net transport was 2 to 3 orders-of-magnitude smaller than in any other season. These results demonstrate that riverine forcing was the primary influence on materials transport in all seasons except fall when tidal forcing was most important. The range of net fluxes (g s?1) for each nutrient was as follows (a negative sign indicates a net export toward the Gulf): NO3 ?, ?0.006 to ?6.69; TKN, 0.09 to ?10.41; NH4 +, ?0.02 to ?1.36; SRP, ?0.001 to ?0.53; TSS, ?2 to ?81. Analysis of nutrient concentrations indicated the marsh/aquatic system removed NO3 ?, SRP, and TSS from the water column from late spring through early fall and released NH4 + and TKN in summer. The results of this study show that net materials export per unit cross section channel area increased as riverine influence increased. 相似文献
5.
Water samples from the Fraser, Skeena and Nass River basins of the Canadian Cordillera were analyzed for dissolved major element concentrations (HCO3−, SO42−, Cl−, Ca2+, Mg2+, K+, Na+), δ13C of dissolved inorganic carbon (δ13CDIC), and δ34S of dissolved sulfate (δ34SSO4) to quantify chemical weathering rates and exchanges of CO2 between the atmosphere, hydrosphere, and lithosphere. Weathering rates of silicates and carbonates were determined from major element mass balance. Combining the major element mass balance with δ34SSO4 (−8.9 to 14.1‰CDT) indicates sulfide oxidation (sulfuric acid production) and subsequent weathering of carbonate and to a lesser degree silicate minerals are important processes in the study area. We determine that on average, 81% of the riverine sulfate can be attributed to sulfide oxidation in the Cordilleran rivers, and that 25% of the total weathering cation flux can be attributed to carbonate and silicate dissolution by sulfuric acid. This result is validated by δ13CDIC values (−9.8 to −3.7‰ VPDB) which represents a mixture of DIC produced by the following weathering pathways: (i) carbonate dissolution by carbonic acid (−8.25‰) > (ii) silicate dissolution by carbonic acid (−17‰) ≈ (iii) carbonate dissolution by sulfuric acid derived from the oxidation of sulfides (coupled sulfide-carbonate weathering) (+0.5‰).δ34SSO4 is negatively correlated with δ13CDIC in the Cordilleran rivers, which further supports the hypothesis that sulfuric acid produced by sulfide oxidation is primarily neutralized by carbonates, and that sulfide-carbonate weathering impacts the δ13CDIC of rivers. The negative correlation between δ34SSO4 and δ13CDIC is not observed in the Ottawa and St. Lawrence River basins. This suggests other factors such as landscape age (governed by tectonic uplift) and bedrock geology are important controls on regional sulfide oxidation rates, and therefore also on the magnitude of sulfide-carbonate weathering—i.e., it is more significant in tectonically active areas.Calculated DIC fluxes due to Ca and Mg silicate weathering by carbonic acid (38.3 × 103 mol C · km−2 · yr−1) are similar in magnitude to DIC fluxes due to sulfide-carbonate weathering (18.5 × 103 mol C · km−2 · yr−1). While Ca and Mg silicate weathering facilitates a transfer of atmospheric CO2 to carbonate rocks, sulfide-carbonate weathering can liberate CO2 from carbonate rocks to the atmosphere when sulfide oxidation exceeds sulfide deposition. This implies that in the Canadian Cordillera, sulfide-carbonate weathering can offset up to 48% of the current CO2 drawdown by silicate weathering in the region. 相似文献
6.
Fluid infiltration and regional metamorphism of the Waits River Formation, north-east Vermont, USA 总被引：2，自引：0，他引：2
Abstract The Siluro-Devonian Waits River Formation of north-east Vermont was deformed, intruded by plutons and regionally metamorphosed during the Devonian Acadian Orogeny. Five metamorphic zones were mapped based on the mineralogy of carbonate rocks. From low to high grade, these are: (1) ankerite-albite, (2) ankerite-oligoclase, (3) biotite, (4) amphibole and (5) diopside zones. Pressure was near 4.5kbar and temperature varied from c. 450° C in the ankerite-albite zone to c. 525° C in the diopside zone. Fluid composition for all metamorphic zones was estimated from mineral equilibria. Average calculated χco2[= CO2/(CO2+ H2O)] of fluid in equilibrium with the marls increases with increasing grade from 0.05 in the ankerite-oligoclase zone, to 0.25 in the biotite zone and to 0.44 in the amphibole zone. In the diopside zone, χCO2 decreases to 0.06. Model prograde metamorphic reactions were derived from measured modes, mineral chemistry, and whole-rock chemistry. Prograde reactions involved decarbonation with an evolved volatile mixture of χCO2 > 0.50. The χCO2 of fluid in equilibrium with rocks from all zones, however, was generally <0.40. This difference attests to the infiltration of a reactive H2O-rich fluid during metamorphism. Metamorphosed carbonate rocks from the formation suggests that both heat flow and pervasive infiltration of a reactive H2O-rich fluid drove mineral reactions during metamorphism. Average time-integrated volume fluxes (cm3 fluid/cm2 rock), calculated from the standard equation for coupled fluid flow and reaction in porous media, are (1) ankerite-oligoclase zone: c. 1 × 104; (2) biotite zone: c. 3 × 104; (3) amphibole zone: c. 10 × 104; and diopside zone: c. 60 × 104. The increase in calculated flux with increasing grade is at least in part the result of internal production of volatiles from prograde reactions in pelitic schists and metacarbonate rocks within the Waits River Formation. The mapped pattern of time-integrated fluxes indicates that the Strafford-Willoughby Arch and the numerous igneous intrusions in the field area focused fluid flow during metamorphism. Many rock specimens in the diopside zone experienced extreme alkali depletion and also record low χCO2. Metamorphic fluids in equilibrium with diopside zone rocks may therefore represent a mixture of acid, H2O-rich fluids given off by the crystallizing magmas, and CO2-H2O fluids produced by devolatilization reactions in the host marls. Higher fluxes and different fluid compositions recorded near the plutons suggest that pluton-driven hydrothermal cells were local highs in the larger regional metamorphic hydrothermal system. 相似文献
7.
The short term climatic sensitivity of carbonate and silicate weathering fluxes: Insight from seasonal variations in river chemistry 总被引：2，自引：0，他引：2
Edward T. Tipper Mike J. Bickle A. Joshua West Hazel J. Chapman 《Geochimica et cosmochimica acta》2006,70(11):2737-2754
Large seasonal variations in the dissolved load of the headwater tributaries of the Marsyandi river (Nepal Himalaya) for major cations and 87Sr/86Sr ratios are interpreted to result from a greater dissolution of carbonate relative to silicate at high runoff. There is up to a 0.003 decrease in strontium isotope ratios and a factor of 3 reduction in the Si(OH)4/Ca ratio during the monsoon. These variations, in small rivers sampling uniform lithologies, result from a different response of carbonate and silicate mineral dissolution to climatic forcing. Similar trends are observed in compiled literature data, from both Indian and Nepalese Himalayan rivers. Carbonate weathering is more sensitive to monsoonal runoff because of its faster dissolution kinetics. Silicate weathering increases relative to carbonate during the dry season, and may be more predominant in groundwater with longer water-rock interaction times. Despite this kinetic effect, silicate weathering fluxes are dominated by the monsoon flux, when between 50% and 70% of total annual silicate weathering flux occurs. 相似文献
8.
Yannick Linard 《Geochimica et cosmochimica acta》2008,72(2):590-601
The enthalpies of solution of La2O3, TiO2, HfO2, NiO and CuO were measured in sodium silicate melts at high temperature. When the heat of fusion was available, we derived the corresponding liquid-liquid enthalpies of mixing. These data, combined with previously published work, provide insight into the speciation reactions in sodium silicate melts. The heat of solution of La2O3 in these silicate solvents is strongly exothermic and varies little with La2O3 concentration. The variation of heat of solution with composition of the liquid reflects the ability of La(III) to perturb the transient silicate framework and compete with other cations for oxygen. The enthalpy of solution of TiO2 is temperature-dependent and indicates that the formation of Na-O-Si species is favored over Na-O-Ti at low temperature. The speciation reactions can be interpreted in terms of recent spectroscopic studies of titanium-bearing melts which identify a dual role of Ti4+ as both a network-former end network-modifier. The heats of solution of oxides of transition elements (Ni and Cu) are endothermic, concentration-dependent and reach a maximum with concentration. These indicate a charge balanced substitution which diminishes the network modifying role of Na+ by addition of Ni2+ or Cu2+. The transition metal is believed to be in tetrahedral coordination, charge balanced by the sodium cation in the melts. 相似文献
9.
James P. McKinley John M. Zachara Steven C. Heald Brian W. Kempshall 《Geochimica et cosmochimica acta》2006,70(8):1873-1887
An alkaline brine containing uranyl (UO22+) leaked to the thick unsaturated zone at the Hanford Site. We examined samples from this zone at microscopic scale to determine the mode of uranium occurrence—microprecipitates of uranyl (UO22+) silicate within lithic-clast microfractures—and constructed a conceptual model for its emplacement, which we tested using a model of reactive diffusion at that scale. The study was driven by the need to understand the heterogeneous distribution of uranium and the chemical processes that controlled it. X-ray and electron microprobe imaging showed that the uranium was associated with a minority of clasts, specifically granitic clasts occupying less than four percent of the sediment volume. XANES analysis at micron resolution showed the uranium to be hexavalent. The uranium was precipitated in microfractures as radiating clusters of uranyl silicates, and sorbed uranium was not observed on other surfaces. Compositional determinations of the 1-3 μm precipitates were difficult, but indicated a uranyl silicate. These observations suggested that uranyl was removed from pore waters by diffusion and precipitation in microfractures, where dissolved silica within the granite-equilibrated solution would cause supersaturation with respect to sodium boltwoodite. This hypothesis was tested using a reactive diffusion model operating at microscale. Conditions favoring precipitation were simulated to be transient, and driven by the compositional contrast between pore and fracture space. Pore-space conditions, including alkaline pH, were eventually imposed on the microfracture environment. However, conditions favoring precipitation were prolonged within the microfracture by reaction at the silicate mineral surface to buffer pH in a solubility limiting acidic state, and to replenish dissolved silica. During this time, uranyl was additionally removed to the fracture space by diffusion from pore space. Uranyl is effectively immobilized within the microfracture environment within the presently unsaturated Vadose Zone. 相似文献
10.
Michael T. Hren C. Page Chamberlain Peter M. Blisniuk 《Geochimica et cosmochimica acta》2007,71(12):2907-2935
The Yarlung Tsangpo-Brahmaputra river drains a large portion of the Himalaya and southern Tibetan plateau, including the eastern Himalayan syntaxis, one of the most tectonically active regions on the globe. We measured the solute chemistry of 161 streams and major tributaries of the Tsangpo-Brahmaputra to examine the effect of tectonic, climatic, and geologic factors on chemical weathering rates. Specifically, we quantify chemical weathering fluxes and CO2 consumption by silicate weathering in southern Tibet and the eastern syntaxis of the Himalaya, examine the major chemical weathering reactions in the tributaries of the Tsangpo-Brahmaputra, and determine the total weathering flux from carbonate and silicate weathering processes in this region. We show that high precipitation, rapid tectonic uplift, steep channel slopes, and high stream power generate high rates of chemical weathering in the eastern syntaxis. The total dissolved solids (TDS) flux from the this area is greater than 520 tons km−2 yr−1 and the silicate cation flux more than 34 tons km−2 yr−1. In total, chemical weathering in this area consumes 15.2 × 105 mol CO2 km−2 yr−1, which is twice the Brahmaputra average. These data show that 15-20% of the total CO2 consumption by silicate weathering in the Brahmaputra catchment is derived from only 4% of the total land area of the basin. Hot springs and evaporite weathering provide significant contributions to dissolved Na+ and Cl− fluxes throughout southern Tibet, comprising more than 50% of all Na+ in some stream systems. Carbonate weathering generates 80-90% of all dissolved Ca2+ and Mg2+ cations in much of the Yarlung Tsangpo catchment. 相似文献
11.
I. S. Peretyazhko E. A. Savina E. A. Khromova N. S. Karmanov A. V. Ivanov 《Petrology》2018,26(2):181-211
The paper presents mineralogical and geochemical data on clinkers and paralavas and on conditions under which they were formed at the Nyalga combustion metamorphic complex, which was recently discovered in Central Mongolia. Mineral and phase assemblages of the CM rocks do not have analogues in the world. The clinkers contain pyrogenically modified mudstone relics, acid silicate glass, partly molten quartz and feldspar grains, and newly formed indialite microlites (phenocrysts) with a ferroindialite marginal zone. In the paralava melts, spinel microlites with broadly varying Fe concentrations and anorthite–bytownite were the first to crystallize, and were followed by phenocrysts of Al-clinopyroxene ± melilite and Mg–Fe olivine. The next minerals to crystallize were Ca-fayalite, kirschsteinite, pyrrhotite, minerals of the rhönite–kuratite series, K–Ba feldspars (celsian, hyalophane, and Ba-orthoclase, Fe3+-hercynite ± (native iron, wüstite, Al-magnetite, and fresnoite), nepheline ± (kalsilite), and later calcite, siderite, barite, celestine, and gypsum. The paralavas contain rare minerals of the rhönite–kuratite series, a new end-member of the rhönite subgroup Ca4Fe 8 2+ Fe 4 3+ O4 [Si8Al4O36], a tobermorite-like mineral Ca5Si5(Al,Fe)(OH)O16 · 5H2O, and high- Ba F-rich mica (K,Ba)(Mg,Fe)3(Al,Si)4O10F2. The paralavas host quenched relics of microemulsions of immiscible residual silicate melts with broadly varying Si, Al, Fe, Ca, K, Ba, and Sr concentrations, sulfide and calcitic melts, and water-rich silicate–iron ± (Mn) fluid media. The clinkers were formed less than 2 Ma ago in various parts of the Choir–Nyalga basin by melting Early Cretaceous mudstones with bulk composition varies from dacitic to andesitic. The pyrogenic transformations of the mudstones were nearly isochemical, except only for volatile components. The CM melt rocks of basaltic andesitic composition were formed via melting carbonate–silicate sediments at temperatures above 1450°C. The Ca- and Fe-enriched and silicaundersaturated paralavas crystallized near the surface at temperatures higher than 900–1100°C and oxygen fugacity \(f_{O_2 }\) between the IW and QFM buffers. In local melting domains of the carbonate–silicate sedimentary rocks and in isolations of the residual melts among the paralava matrix the fluid pressure was higher than the atmospheric one. The bulk composition, mineral and phase assemblages of CM rocks of the Nyalga complex are very diverse (dacitic, andesitic, basaltic andesitic, basaltic, and silica-undersaturated mafic) because the melts crystallized under unequilibrated conditions and were derived by the complete or partial melting of clayey and carbonate–silicate sediments during natural coal fires. 相似文献
12.
Calcium carbonate dissolution in deep sea sediments: reconciling microelectrode, pore water and benthic flux chamber results 总被引：1，自引：0，他引：1
We report the benthic fluxes of O2, titration alkalinity (TA), Ca2+, NO3−, PO43−, and Si(OH)4 from in situ benthic flux chamber incubations on the Ceara Rise and Cape Verde Plateau and compare them to previously published results. We find within analytical uncertainty that the TA flux is twice the calcium flux, suggesting that dissolution/precipitation of CaCO3 is the principal mechanism controlling benthic TA and Ca2+ fluxes. At sites where the sediments contain significant (>35%) CaCO3 and the overlying waters are supersaturated with respect to CaCO3, the ratios of the total dissolution rate to the remineralization rate are significantly less than at all other study sites. We propose that these observations can be explained by precipitation of fresh CaCO3 at the supersaturated sediment surface followed by redissolution deeper in the sediments because of metabolically-produced CO2. A numerical simulation is presented to demonstrate the feasibility of this explanation. In addition, surface exchange reactions in high-CaCO3 sediments coupled with high rates of particle mixing may also impact rates of metabolic dissolution and depress chamber-derived estimates of carbonate alkalinity and calcium benthic fluxes. These results suggest that at supersaturated, high CaCO3 locations, previous models of sediment diagenesis may have overestimated the impact of metabolic dissolution on the preservation of CaCO3 deposited on the sea floor. 相似文献
13.
Some of the most vanadium-rich silicate minerals known are present in green mica schist from the Hemlo gold deposit, Ontario, Canada. Vanadium-rich silicate minerals include green mica (up to 17.6 wt. % V2O3), phlogopite (10.1 wt. % V2O3), pumpellyite (25.7 wt. % V2O3), garnet (18.5 wt. % V2O3), epidote-group minerals (9.1 wt. % V2O3), antimonian vesuvianite (4.3 wt. % V2O3), and titanite (18.5 wt. % V2O5). In addition, minor amounts of V (<2 wt. % V2O3) are present in tourmaline, chlorite, talc and tremolite in other lithologies of the Hemlo deposit. The principal substitution that incorporates V into most of these silicate minerals is Al3+=V3+ in octahedral positions. Vanadium is incorporated into phlogopite mainly by the two substitutions: 3Mg2+ =2V3++ and VIMg2++IVSi4+=VIV3+ +IVAl3+, and all of the three substitutions Ti4++O2- =V3++(OH,F)-, Ti4+=V4+, and 5Ti4+=4V5+ + may have operated in titanite.Vanadium-enriched green mica schist from the Hemlo gold deposit is characterized by uniform Ti/Zr ratios, systematically low Ti, Ni, Co and Sc abundances, and low levels of incompatible elements Th, U, Hf and Zr and is distinct in these respects from its Cr-enriched counterpart. These geochemical features, along with textural evidence (relict quartz and oligoclase phenocrysts), indicate that the V-enriched green mica schist from Hemlo was most likely derived mainly from quartz-oligoclase porphyry. However, its anomalously high V and Cr contents were probably introduced metasomatically from local maficultramafic sources and were fixed in green mica and oxides during the waning of a second regional metamorphism. Vanadium was further remobilized, and its concentration probably enhanced, during the late hydrothermal alteration, which resulted in the formation of the characteristic V-rich calc-silicate minerals. 相似文献
14.
Methane and CO2 emissions from the two most active mud volcanoes in central Japan, Murono and Kamou (Tokamachi City, Niigata Basin), were measured in from both craters or vents (macro-seepage) and invisible exhalation from the soil (mini- and microseepage). Molecular and isotopic compositions of the released gases were also determined. Gas is thermogenic (δ13CCH4 from −32.9‰ to −36.2‰), likely associated with oil, and enrichments of 13C in CO2 (δ13CCO2 up to +28.3‰) and propane (δ13CC3H8 up to −8.6‰) suggest subsurface petroleum biodegradation. Gas source and post-genetic alteration processes did not change from 2004 to 2010. Methane flux ranged within the orders of magnitude of 101-104 g m−2 d−1 in macro-seeps, and up to 446 g m−2 d−1 from diffuse seepage. Positive CH4 fluxes from dry soil were widespread throughout the investigated areas. Total CH4 emission from Murono and Kamou were estimated to be at least 20 and 3.7 ton a−1, respectively, of which more than half was from invisible seepage surrounding the mud volcano vents. At the macro-seeps, CO2 fluxes were directly proportional to CH4 fluxes, and the volumetric ratios between CH4 flux and CO2 flux were similar to the compositional CH4/CO2 volume ratio. Macro-seep flux data, in addition to those of other 13 mud volcanoes, supported the hypothesis that molecular fractionation (increase of the “Bernard ratio” C1/(C2 + C3)) is inversely proportional to gas migration fluxes. The CH4 “emission factor” (total measured output divided by investigated seepage area) was similar to that derived in other mud volcanoes of the same size and activity. The updated global “emission-factor” data-set, now including 27 mud volcanoes from different countries, suggests that previous estimates of global CH4 emission from mud volcanoes may be significantly underestimated. 相似文献
15.
Sediment oxygen uptake and net sediment-water fluxes of dissolved inorganic and organic nitrogen and phosphorus were measured at two sites in Fourleague Bay, Louisiana, from August 1981, through May 1982. This estuary is an extension of Atchafalaya Bay which receives high discharge and nutrient loading from the Atchafalaya River. Sediment O2 uptake averaged 49 mg m?2 h?1. On the average, ammonium (NH4 +) was released from the sediments (mean flux =+129 μmol m?2 h?1), and NO3 ? was taken up (mean flux =?19 μmol m?2h?1). However, very different NO3 ? fluxes were observed at the two sites, with sediment uptake at the upper, river-influenced, high NO3 ? site (mean flux =?112 μmol m?2 h?1) and release at the lower, marine-influenced low NO3 ? site (mean flux =+79 μmol m?2 h?1). PO4 3? fluxes were low and often negative (mean flux =?8 μmol m?2 h?1), while dissolved organic phosphorus fluxes were high and positive (mean flux =+124 μmol m?2 h?1). Dissolved organic nitrogen fluxes varied greatly, ranging from a mean of +305 μmol m?2 h?1 at the lower bay, to ?710 μmol m?2 h?1 at the upper bay. Total dissolved nitrogen and phosphorus fluxes indicated the sediments were a nitrogen (mean flux =+543 μmol m?2 h?1) and phosphorus source (mean flux =+30 μmol m?2 h?1) at the lower bay, and a nitrogen sink (mean flux =?553 μmol m?2 h?1) and phosphorus source (mean flux =+17 μmol m?2 h?1) in the upper bay. Mean annual O∶N ration of the positive inorganic sediment fluxes were 27∶1 at the upper bay and 18∶1 at the lower bay. Based on these data we hypothesize that nitrification and denitrification are important sediment processes in the upper bay. We further hypothesize that Atchafalaya River discharge affects sediment-water fluxes through seasonally high nutrient loading which leads to net nutrient uptake by sediments in the upper bay and release in the lower bay, where there is less river influnces. 相似文献
16.
Chemical and Strontium Isotopic Compositions of the Hanjiang Basin Rivers in China: Anthropogenic Impacts and Chemical Weathering 总被引：1，自引：0，他引：1
The Hanjiang River, the largest tributaries of the Changjiang (Yangtze) River, is the water source area of the Middle Route
of China’s South-to-North Water Transfer Project. The chemical and strontium isotopic compositions of the river waters are
determined with the main purpose of understanding the contribution of chemical weathering processes and anthropogenic inputs
on river solutes, as well as the associated CO2 consumption in the carbonate-dominated basin. The major ion compositions of the Hanjiang River waters are characterized by
the dominance of Ca2+ and HCO3
−, followed by Mg2+ and SO4
2−. The increase in TDS and major anions (Cl−, NO3
−, and SO4
2−) concentrations from upstream to downstream is ascribed to both extensive influences from agriculture and domestic activities
over the Hanjiang basin. The chemical and Sr isotopic analyses indicate that three major weathering sources (dolomite, limestone,
and silicates) contribute to the total dissolved loads. The contributions of the different end-members to the dissolved load
are calculated with the mass balance approach. The calculated results show that the dissolved load is dominated by carbonates
weathering, the contribution of which accounts for about 79.4% for the Hanjiang River. The silicate weathering and anthropogenic
contributions are approximately 12.3 and 6.87%, respectively. The total TDS fluxes from chemical weathering calculated for
the water source area (the upper Hanjiang basin) and the whole Hanjiang basin are approximately 3.8 × 106 and 6.1 × 106 ton/year, respectively. The total chemical weathering (carbonate and silicate) rate for the Hanjiang basin is approximately
38.5 ton/km2/year or 18.6 mm/k year, which is higher than global mean values. The fluxes of CO2 consumption by carbonate and silicate weathering are estimated to be 56.4 × 109 and 12.9 × 109 mol/year, respectively. 相似文献
17.
A detailed geochemical study on river waters of the Australian Victorian Alps was carried out to determine: (i) the relative significance of silicate, carbonate, evaporite and sulfide weathering in controlling the major ion composition and; (ii) the factors regulating seasonal and spatial variations of CO2 consumption via silicate weathering in the catchments. Major ion chemistry implies that solutes are largely derived from evaporation of precipitation and chemical weathering of carbonate and silicate lithologies. The input of solutes from rock weathering was determined by calculating the contribution of halite dissolution and atmospheric inputs using local rain and snow samples. Despite the lack of carbonate outcrops in the study area and waters being undersaturated with respect to calcite, the dissolution of vein calcite accounts for up to 67% of the total dissolved cations, generating up to 90% of dissolved Ca and 97% of Mg. Dissolved sulfate has δ34S values of 16 to 20‰CDT, indicating that it is derived predominantly from atmospheric deposition and minor gypsum weathering and not from bacterial reduction of FeS2. This militates against sulphuric acid weathering in Victorian rivers. Ratios of Si vs. the atmospheric corrected Na and K concentrations range from ~ 1.1 to ~ 4.3, suggesting incongruent weathering from plagioclase to smectite, kaolinite and gibbsite.Estimated long-term average CO2 fluxes from silicate weathering range from ~ 0.012 × 106 to 0.039 × 106 mol/km2/yr with the highest values in rivers draining the basement outcrops rather than sedimentary rocks. This is about one order of magnitude below the global average which is due to low relief, and the arid climate in that region. Time series measurements show that exposure to lithology, high physical erosion and long water–rock contact times dominate CO2 consumption fluxes via silicate weathering, while variations in water temperature are not overriding parameters controlling chemical weathering. Because the atmospheric corrected concentrations of Na, K and Mg act non-conservative in Victorian rivers the parameterizations of weathering processes, and net CO2 consumption rates in particular, based on major ion abundances, should be treated with skepticism. 相似文献
18.
We continuously measured dissolved silicate concentrations and fluxes discharged from various Rhode River subwatersheds for a period of 14 yr from 1984 to 1998 and for 15 mo in 1971–1972. We also measured dissolved silicate concentrations along a transect from the head of the tide in Rhode River estuary to Chesapeake Bay. The average concentration of dissolved silicate discharged from the Rhode River watershed was 10.8 mg Si l?1. There were consistent and significant differences in silicate concentrations discharged over time and space among subwatersheds. Mean annual silicate flux from the watershed was 26.6 kg Si ha?1 and 93% of this occurred during the winter and spring seasons. There were large interannual variations in silicate flux, due primarily to differences in precipitation and water discharge, rather than silicate concentration. Land use had little or no effect on silicate flux from various subwatersheds. Silicate concentrations discharged from a subset of subwatersheds in 1995–1996 were 25% to 35% lower than in a period with similar precipitation in 1971–1972. Mean annual concentrations of silicate discharged from nine subwatersheds have been declining about 1.5% yr?1 or by 0.21–0.26 mg Si l?1 yr?1 over the last 25 yr. Despite high average silicate fluxes from the watershed, at times the Rhode River estuary developed low dissolved silicate concentrations, which could have been limiting to the growth of diatoms. Examples were in the spring after a winter with low watershed discharge (as low as 0.019 mg Si l?1 in 1995) and after protracted drought (as low as 0.041 mg Si l?1 in 1993). 相似文献
19.
We have investigated the geochemistry of supraglacial streams on the Canada Glacier, Taylor Valley, Antarctica during the
2001–2002 austral summer. Canada Glacier supraglacial streams represent the link between primary precipitation (i.e. glacier
snow) and proglacial Lake Hoare. Canada Glacier supraglacial stream geochemistry is intermediate between glacier snow and
proglacial stream geochemistry with average concentrations of 49.1 μeq L−1 Ca2+, 19.9 μeq L−1 SO42−, and 34.3 μeq L−1 HCO3−. Predominant west to east winds lead to a redistribution of readily soluble salts onto the glacier surface, which is reflected
in the geochemistry of the supraglacial streams. Western Canada Glacier supraglacial streams have average SO42−:HCO3− equivalent ratios of 1.0, while eastern supraglacial streams average 0.5, suggesting more sulfate salts reach and dissolve
in the western supraglacial streams. A graph of HCO3− versus Ca2+ for western and eastern supraglacial streams had slopes of 0.87 and 0.72, respectively with R2 values of 0.84 and 0.83. Low concentrations of reactive silicate (> 10 μmol L−1) in the supraglacial streams suggested that little to no silicate weathering occurred on the glacier surface with the exception
of cryoconite holes (1000 μmol L−1). Therefore, the major geochemical weathering process occurring in the supraglacial streams is believed to be calcite dissolution.
Proglacial stream, Anderson Creek, contains higher concentrations of major ions than supraglacial streams containing 5 times
the Ca2+ and 10 times the SO42−. Canada Glacier proglacial streams also contain higher concentrations (16.6–30.6 μeq L−1) of reactive silicate than supraglacial streams. This suggests that the controls on glacier meltwater geochemistry switch
from calcite and gypsum dissolution to both salt dissolution and silicate mineral weathering as the glacier meltwater evolves.
Our chemical mass balance calculations indicate that of the total discharge into Lake Hoare, the final recipient of Canada
Glacier meltwater, 81.9% is from direct glacier runoff and 19.1% is from proglacial Andersen Creek. Although during a typical,
low melt ablation season Andersen Creek contributes over 40% of the water added to Lake Hoare, its overall chemical importance
is diluted by the direct inputs from Canada Glacier during high flow years. Decadal warming events, such as the 2001–2002
austral summer produce supraglacial streams that are a major source of water to Lake Hoare. 相似文献
20.
Mud volcanoes are important pathways for CH4 emission from deep buried sediments; however, the importance of gas fluxes have hitherto been neglected in atmospheric source budget considerations. In this study, gas fluxes have been monitored to examine the stability of their chemical compositions and fluxes spatially, and stable C isotopic ratios of CH4 were determined, for several mud volcanoes on land in Taiwan. The major gas components are CH4 (>90%), “air” (i.e. N2 + O2 + Ar, 1–5%) and CO2 (1–5%) and these associated gas fluxes varied slightly at different mud volcanoes in southwestern Taiwan. The Hsiao-kun-shui (HKS) mud volcano emits the highest CH4 concentration (CH4 > 97%). On the other hand, the Chung-lun mud volcano (CL) shows CO2 up to 85%, and much lower CH4 content (<37%). High CH4 content (>90%) with low CO2 (<0.2%) are detected in the mud volcano gases collected in eastern Taiwan. It is suggestive that these gases are mostly of thermogenic origin based on C1 (methane)/C2 (ethane) + C3 (propane) and δ13CCH4 results, with the exception of mud volcanoes situated along the Gu-ting-keng (GTK) anticline axis showing unique biogenic characteristics. Only small CH4 concentration variations, <2%, were detected in four on-site short term field-monitoring experiments, at Yue-shi-jie A, B, Kun-shui-ping and Lo-shan A. Preliminary estimation of CH4 emission fluxes for mud volcanoes on land in Taiwan fall in a range between 980 and 2010 tons annually. If soil diffusion were taken into account, the total amount of mud volcano CH4 could contribute up to 10% of total natural CH4 emissions in Taiwan. 相似文献