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1.
Processes controlling the nitrogen (N) exchange between water and sediment in eutrophic Lake Sempach were studied using three different independent methods: benthic flux chambers, interstitial water data and hypolimnetic mass balances. The sediments released NH 4 + (1.1–16.1 mmoles m–2 d–1), NO 2 - (0.1–0.4 mmoles m–2 d–1) and dissolved organic N (<0.25 mmoles m–2 d–1). A net NO 3 - consumption (2.4–11.1 mmoles m–2 d–1) related to the NO 3 - concentrations in the overlying water was observed in all benthic chamber experiments. The flux of the reactive species NO 3 - and NH 4 + was found to depend on hydrodynamic conditions in the water overlying the sediment. For this reason, benthic chambers overestimated the fluxes of inorganic N compared to the other methods. Thus, in short-term flux chamber experiments the sediment may either become a sink or a source for inorganic N depending on the O2 concentration in the water overlying the sediment and the stirring rate. As demonstrated with a15NO 3 - experiment, nitrate-ammonification accounted for less than 12% of the total NO 3 - consumption. After six years of artificial oxygenation in Lake Sempach, a decrease in hypolimnetic total inorganic nitrogen (TIN) was observed in the last two years. The occurrence of dense mats of H2S-oxidizingBeggiatoa sp. indicated micro-aerobic conditions at the sediment surface. Under these conditions, a shorter distance between the ecological niches of nitrifying and denitrifying bacteria, and therefore a faster NO 3 - -transport, can possibly explain the lowering of TIN by enhanced net denitrification.  相似文献   

2.
The flow of carbon and nitrogen in sediments of the far northern and northern sections of the Great Barrier Reef continental shelf was examined. Most of the organic carbon (81–94%) and total nitrogen (74–92%) depositing to the seabed was mineralized, with burial of carbon (6–19%) and nitrogen (8–20%) being proportionally less on this tropical shelf compared with other non-deltaic shelves. Differences in carbon and nitrogen mineralization among stations related best to water depth and proximity to river basins, with rates of mineralization based on net ∑CO2 production ranging from 17 to 39 ( mean=23) mmol C m−2 d−1. The overall ratio of O2:CO2 flux was 1.3, close to the Redfield ratio, implying that most organic matter mineralized was algal. Sulfate reduction was estimated to account for ≈30% (range: 6–62%), and denitrification for ≈5% (range: 2–13%), of total C mineralization; there was no measurable CH4 production. Discrepancies between ∑CO2 production across the sediment–water interface and sediment incubations suggest that as much as 5 mmol m−2 d−1 (≈25% of ∑CO2 flux) was involved in carbonate mineral formation. Most microbial activity was in the upper 20 cm of sediment. Rates of net NH4+ production ranged from 1.6 to 2.7 mmol N m−2 d−1, with highly variable N2 fixation rates contributing little to total N input. Ammonification and nitrification rates were sufficient to support rapid rates of denitrification (range: 0.1–12.4 mmol N m−2 d−1). On average, nearly 50% of total N input to the shelf sediment was denitrified. The average rates of sedimentation, mineralization, and burial of C and N were greater in the northern section of the shelf than in the far northern section, presumably due to higher rainfall and river discharge, as plankton production was similar between regions. The relative proportion of plankton primary production remineralized at the seafloor was in the range of 30–50% which is at the high end of the range found on other shelves. The highly reactive nature of these sediments is attributed to the deposition of high-quality organic material as well as to the shallowness of the shelf, warm temperatures year-round, and a variety of physical disturbances (cyclones, trawling) fostering physicochemical conditions favorable for maintaining rapid rates of microbial metabolism. The rapid and highly efficient recycling of nutrients on the inner and middle shelf may help to explain why the coral reefs on the outer shelf have remained unscathed from increased sediment delivery since European settlement.  相似文献   

3.
Hydrographic and biogeochemical observations were conducted along the longitudinal section from Ise Bay to the continental margin (southern coast of Japan) to investigate changes according to the Kuroshio path variations during the summer. The strength of the uplift of the cold deep water was influenced by the surface intrusion of the Kuroshio water to the shelf region. When the intrusion of the Kuroshio surface water to the shelf region was weak in 2006, the cold and NO3−-rich shelf water intruded into the bottom layer in the bay from the shelf. This bottom intrusion was intensified by the large river discharge. The nitrogen isotope ratio (δ15N) of NO3− (4–5‰) in the bottom bay water was same as that in the deeper NO3− over the shelf, indicating the supply of new nitrogen to the bay. The warm and NO3−-poor shelf water intruded into the middle layer via the mixing region at the bay mouth when the Kuroshio water distributed in the coastal areas off Ise Bay in 2005. The regenerated NO3− with isotopically light nitrogen (δ15N=−1‰) was supplied from the shelf to the bay. This NO3− is regenerated by the nitrification in the upper layer over the shelf. The contribution rate of regenerated NO3− over the shelf to the total NO3− in the subsurface chlorophyll maximum layer in the bay was estimated at 56% by a two-source mixing model coupled with the Rayleigh equation.  相似文献   

4.
The consequences of a coastal upwelling event on physical and chemical patterns were studied in the central Gulf of Finland. Weekly mapping of hydrographical and -chemical fields were carried out across the Gulf between Tallinn and Helsinki in July–August 2006. In each survey, vertical profiles of temperature and salinity were recorded at 27 stations and water samples for chemical analyses (PO43−, NO2−+NO3−) were collected at 14 stations along the transect. An ordinary distribution of hydrophysical and -chemical variables with the seasonal thermocline at the depths of 10–20 m was observed in the beginning of the measurements in July. Nutrient concentrations in the upper mixed layer were below the detection limit and nutriclines were located just below or in the lower part of the thermocline. In the first half of August, a very intense upwelling event occurred near the southern coast of the Gulf when waters with low temperature and high salinity from the intermediate layer surfaced. High nutrient concentrations were measured in the upwelled water – 0.4 μmol l−1 of phosphates and 0.6 μmol l−1 of nitrates+nitrites. We estimated the amount of nutrients transported into the surface layer as 238–290 tons of phosphorus (P)-PO43− and 175–255 tons of N-NOx for a 12 m thick, 20 km wide and 100 km long coastal stretch. Taking into account a characteristic along-shore extension of the upwelling of 200 km, the phosphate-phosphorus amount is approximately equal to the average total monthly riverine load of phosphorus to the Gulf of Finland. It is shown that TS-characteristics of water masses and vertical distribution of nutrients along the study transect experienced drastic changes caused by the upwelling event in the entire studied water column. TS-analysis of profiles obtained before and during the upwelling event suggests that while welled up, the cold intermediate layer water was mixed with the water from the upper mixed layer with a share of 85% and 15%. We suggest that the coastal upwelling events contribute remarkably to the vertical mixing of waters in the Gulf of Finland. Intrusions of nutrient-rich waters along the inclined isopycnal surfaces in the vicinity of upwelling front were revealed. The upwelling event widened the separation of phosphocline and nitracline which in turn prevented surfacing of nitrate+nitrite-nitrogen during the next upwelling event observed a week after the upwelling relaxation. A suggestion is made that such widening of nutricline separation caused by similar upwelling events in early summer could create favourable conditions for late summer cyanobacterial blooms.  相似文献   

5.
The Long Valley Exploratory Well, at the center of the Resurgent Dome of Long Valley caldera, penetrated pre-caldera basement rocks at a depth of 2101.72–2313.0 m, beneath the caldera-forming Bishop Tuff and post-caldera Early Rhyolite. The basement rocks contain prominent quartzites, with ubiquitous milky white quartz veins (with minor calcite and pyrite) and fractures of varied orientation and geometry. The other members of the basement sequence are very fine-grained quartz-rich graphitic pelites with calcite veins, spotted hornfels, and shallow intrusive rocks. Previous studies established the presence of a post-caldera, paleohydrothermal system (500–100 ka) to a depth of 2000 m that affected the Bishop Tuff and a recent (40 ka to present) hydrothermal system at shallow depth (<1 km). The deeper extent of these hydrothermal activities is established in this paper by a detailed oxygen isotope analysis of the drill core samples. 238 analyses of δ18O in 50 quartz veins within the 163.57 m depth interval of basement rocks reveal extreme heterogeneity in δ18O values (8–19.5‰). Majorities of the 84 bulk analyses of quartzites show variation of δ18O within a narrow range of 14–16‰. However, certain samples of these quartzites near the contacts with veins and fractures exhibit sharp drops in δ18O. The interbedded pelitic rocks and spotted hornfels have whole-rock δ18O ranging from 2.2 to 11.8‰. Clear, euhedral vuggy quartz that partially fills earlier open fractures in both the quartzites and quartz veins, has distinctive δ18O, ranging between −3.2 and +8.4‰. Low values of δ18O are also found in the hydrothermal minerals and whole rocks adjacent to the thin veins, clearly indicating infiltration of meteoric water. Three distinct observed patterns of fractionation in δ18O between veins and host quartzites are analyzed with the principles of mass balance, equilibrium oxygen isotope fractionation in closed system, and kinetically controlled oxygen isotope exchange in an open system. This analysis suggests that the early quartz veins formed due to a magmatic-hydrothermal activity with no influx of external water once the system comprising the sedimentary envelope and a magmatic-hydrothermal fluid phase became closed. Two-stage isotopic exchange processes caused fractionation in the δ values that originally formed arrays with slope 1 in a δvein quartz–δhost quartzite space. Another array in the same space, with near zero slope was also formed due to variation in temperature, initial isotopic compositions of the quartzite sequence and the fluid phase. Variation in temperature was mostly in the range of 300–400°C giving Δ (=δvein quartz–δhost quartzite)≈−2.8 to +2.8. The δ18O of the fluid could range from −5 to +10; however a narrower range of +5 to +10 can explain the data. This episode of hydrothermal activity could take place either as a single pulse or in multiple pulses but each as a closed system. A later, fracture-controlled, meteoric water (δ18O−0.46 to −12.13) flow and interaction (at 250°C) is interpreted from the analysis of δ18O values of the coexisting quartz and calcite pairs and existence of markedly 18O-depleted pelitic horizons interbedded with 18O-enriched quartzite layers. Thus, the interpreted earlier magmatic-hydrothermal activity was overprinted by a later meteoric-hydrothermal activity that resulted in steep arrays of δ18O values in the δvein quartz–δhost quartzite space. Calculations show that the likely life span of the post-caldera, hydrothermal activity in the depth range of 2.1–2.3 km beneath Long Valley was 0.08–0.12 Ma. Diffusive ±advective transport of oxygen isotopes from fracture-channelized meteoric water to nearly impermeable wall rocks caused a lowering of δ18O values in the quartz over short distances and in calcites over greater distances. Thus, the hydrothermal activity appears pervasive even though the meteoric water flow was primarily controlled by fractures.  相似文献   

6.
Polyfluorinated compounds (PFCs) were investigated in waste water treatment plant (WWTP) effluents and surface waters of the River Elbe from samples collected in 2007. Concentrations of various PFCs, including C4–C8 perfluorinated sulfonates (PFSAs), C6 and C8 perfluorinated sulfinates, 6:2 fluorotelomer sulfonate, C5–C13 perfluorinated carboxylic acids (PFCAs), C4 and C8 perfluoroalkyl sulfonamides and 6:2, 8:2 and 10:2 unsaturated fluorotelomercarboxylic acids were quantified. ∑PFC concentrations of the river water ranged from 7.6 to 26.4 ng L−1, whereas ∑PFC concentrations of WWTP effluents were approximately 5–10 times higher (30.5–266.3 ng L−1), indicating that WWTPs are potential sources of PFCs in the marine environment. PFC patterns of different WWTP effluents varied depending on the origin of the waste water, whereas the profile of PFC composition in the river water was relatively constant. In both kinds of water samples, perfluorooctanoic acid (PFOA) was the major PFC, whereas perfluorobutane sulfonate (PFBS) was the predominant PFSA.  相似文献   

7.
Gas concentrations and isotopic compositions of water have been measured in hydrothermal waters from 13°N on the East Pacific Rise. In the most Mg-depleted samples ( 5 × 10−3 moles/kg) the gas concentrations are: 3–4.5 × 10−5 cm3 STP/kg helium, 0.62–1.24 cm3 STP/kg CH4, 10.80–16.71 × 10−3 moles/kg CO2. The samples contain large quantities (95–126 cm3/kg) of H2 and some carbon monoxide (0.26–0.36 cm3/kg) which result from reaction with the titanium sampling bottles. δ13C in methane and CO2 (−16.6 to −19.5 and −4.1 to −5.5 respectively) indicate temperatures between 475 and 550°C, whereas δ13CCO is compatible with formation by reduction of CO2 on Ti at 350°C close to the sampling temperature.3He/4He are very homogeneous at (7.5 ± 0.1)RA(3He/4He = 1.0 × 10−5) and very similar to already published data as well as CH4/3He ratios between 1.4 and 2.1 × 106.18O and D in water show enrichments from 0.39 to 0.69‰ and from 0.62 to 1.49‰ respectively. These values correspond to W/R ratios of 0.4–7. The distinct18O enrichments indicate that the isotopic composition of the oceans is not completely buffered by the hydrothermal circulations. The3He-enthalpy relationship is discussed in terms of both hydrothermal heat flux and3He mantle flux.  相似文献   

8.
Samples from Kawah Ijen crater lake, spring and fumarole discharges were collected between 1990 and 1996 for chemical and isotopic analysis. An extremely low pH (<0.3) lake contains SO4–Cl waters produced during absorption of magmatic volatiles into shallow ground water. The acidic waters dissolve the rock isochemically to produce “immature” solutions. The strong D and 18O enrichment of the lake is mainly due to enhanced evaporation at elevated temperature, but involvement of a magmatic component with heavy isotopic ratios also modifies the lake D and 18O content. The large ΔSO4–S0 (23.8–26.4‰) measured in the lake suggest that dissolved SO4 forms during disproportionation of magmatic SO2 in the hydrothermal conduit at temperatures of 250280°C. The lake δ18OSO4 and δ18OH2O values may reflect equilibration during subsurface circulation of the water at temperatures near 150°C. Significant variations in the lake's bulk composition from 1990 to 1996 were not detected. However, we interpret a change in the distribution and concentration of polythionate species in 1996 as a result of increased SO2-rich gas input to the lake system.Thermal springs at Kawah Ijen consist of acidic SO4–Cl waters on the lakeshore and neutral pH HCO3–SO4–Cl–Na waters in Blawan village, 17 km from the crater. The cation contents of these discharges are diluted compared to the crater lake but still do not represent equilibrium with the rock. The SO4/Cl ratios and water and sulfur isotopic compositions support the idea that these springs are mixtures of summit acidic SO4–Cl water and ground water.The lakeshore fumarole discharges (T=170245°C) have both a magmatic and a hydrothermal component and are supersaturated with respect to elemental sulfur. The apparent equilibrium temperature of the gas is 260°C. The proportions of the oxidized, SO2-dominated magmatic vapor and of the reduced, H2S-dominated hydrothermal vapor in the fumaroles varied between 1979 and 1996. This may be the result of interaction of SO2-bearing magmatic vapors with the summit acidic hydrothermal reservoir. This idea is supported by the lower H2S/SO2 ratio deduced for the gas producing the SO4–Cl reservoir feeding the lake compared with that observed in the subaerial gas discharges. The condensing gas may have equilibrated in a liquid–vapor zone at about 350°C.Elemental sulfur occurs in the crater lake environment as banded sediments exposed on the lakeshore and as a subaqueous molten body on the crater floor. The sediments were precipitated in the past during inorganic oxidation of H2S in the lake water. This process was not continuous, but was interrupted by periods of massive silica (poorly crystallized) precipitation, similar to the present-day lake conditions. We suggest that the factor controlling the type of deposition is related to whether H2S- or silica-rich volcanic discharges enter the lake. This could depend on the efficiency with which the lake water circulates in the hydrothermal cell beneath the crater. Quenched liquid sulfur products show δ34S values similar to those found in the banded deposits, suggesting that the subaqueous molten body simply consists of melted sediments previously accumulated at the lake bottom.  相似文献   

9.
Tropical mobile mud belts represent a major class of biogeochemical and diagenetic systems characterized by extensive and frequent physical reworking of fine-grained, organic-rich deposits underlying oxygenated waters. Large regions of the Gulf of Papua, Papua New Guinea deltaic complex are dominated by such conditions. A reworked mud belt lies within the inner shelf between 10 and 20 m depth on a sedimentary clinoform derived from coalescing deltas. Deposits across the topset are typically suboxic, nonsulfidic over the upper 0.5–1 m, and have low to moderate maximum pore water concentrations of dissolved Fe(II) and Mn(II) (100–200, but up to 800 μM). Sediments are reactive, with surficial ΣCO2 production 0.1–0.3 mM d−1 and benthic O2 fluxes 23±15 mmol m−2 d−1 (upper 20 cm). The highest rates occur within inner topset deposits (10–20 m) and near the high accumulation rollover region of the topset–foreset beds (40–50 m). Lower rates are found inshore along intertidal channels—mangrove fringe and within scoured or exposed consolidated deposits of the middle topset region. Remineralization rate patterns are independent of relative dominance by terrestrial or marine carbon in sediments. Dissolved O2 usually penetrates 2–5 mm into surface sediments when macrofaunal burrows are absent. More than 75% of the highly reactive sedimentary Fe(III) pool (350–400 μmol g−1) is typically diagenetically reduced in the upper 0.5 m. Pore water can be measureably depleted at depths >0.5 m, but dissolved H2S generally remains below detection over the upper 1–2 m. As in other deltaic topset regions, concentration gradients often indicate that compared to many marine deposits of similar sediment accumulation rates, relatively refractory Corg is supplied to the SO4 reducing zone. Sedimentary C/S ratios are 4–6 within the suboxic topset regions but decrease to <3 in offshore foreset beds where sulfidic diagenesis dominates. Only 15–20% of the diagenetically reduced Fe(II) is pyritic and a maximum of 10–25% is carbonate, implying that most Fe(II) is associated with authigenic or lithogenic silicates or oxides. The dominance of suboxic, nonsulfidic diagenetic processes reflect coupling between delivery of oxide-rich terrestrial debris, remobilization and reoxidation of deposits, and repetitive entrainment/remineralization of both labile and refractory organics. Distinct sedimentary indicators of reactive, suboxic mobile mud belts within tropical climatic zones are: abundant total highly reactive Fe (ΣFeR )>300 μmol g−1; most reactive Fe is diagenetically reduced (ΣFe(II)/ΣFeR0.7–0.8); the proportion of diagenetically reduced Fe present as pyrite is low (Py–Fe(II)<0.2); C/S 4–8; and Corg/particle surface area <0.4 (mg C m−2). These depositional environments must be most common in tropical climates during high sea stand.  相似文献   

10.
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11.
Isotopic compositions were determined for hydrothermal quartz, calcite, and siderite from core samples of the Newberry 2 drill hole, Oregon. The δ15O values for these minerals decrease with increasing temperatures. The values indicate that these hydrothermal minerals precipitated in isotopic equilibrium with water currently present in the reservoirs. The δ18O values of quartz and calcite from the andesite and basalt flows (700–932 m) have isotopic values which require that the equilibrated water δ18O values increase slightly (− 11.3 to −9.2‰) with increasing measured temperatures (150–265°C). The lithic tuffs and brecciated lava flows (300–700 m) contain widespread siderite. Calculated oxygen isotopic compositions of waters in equilibrium with siderite generally increase with increasing temperatures (76–100°C). The δ18O values of siderite probably result from precipitation in water produced by mixing various amounts of the deep hydrothermal water (− 10.5 ‰) with meteoric water (− 15.5 ‰) recharged within the caldera. The δ13C values of calcite and siderite decrease with increasing temperatures and show that these minerals precipitated in isotopic equilibrium with CO2 of about −8 ‰.The δ18O values of weakly altered (<5% alteration of plagioclase) whole-rock samples decrease with increasing temperatures above 100°C, indicating that exchange between water and rock is kinetically controlled. The water/rock mass ratios decrease with decreasing temperatures. The δ18O values of rocks from the bottom of Newberry 2 show about 40% isotopic exchange with the reservoir water.The calculated δ18O and δD values of bottom hole water determined from the fluid produced during the 20 hour flow test are −10.2 and −109‰, respectively. The δD value of the hydrothermal water indicates recharge from outside the caldera.  相似文献   

12.
Kawah Putih is a summit crater of Patuha volcano, West Java, Indonesia, which contains a shallow, 300 m-wide lake with strongly mineralized acid–sulfate–chloride water. The lake water has a temperature of 26–34°C, pH=<0.5–1.3, Stot=2500–4600 ppm and Cl=5300–12 600 ppm, and floating sulfur globules with sulfide inclusions are common. Sulfur oxyanion concentrations are unusually high, with S4O62−+S5O62−+S6O62−=2400 – 4200 ppm. Subaerial fumaroles (<93°C) on the lake shore have low molar SO2/H2S ratios (<2), which is a favorable condition to produce the observed distribution of sulfur oxyanion species. Sulfur isotope data of dissolved sulfate and native sulfur show a significant 34S fractionation (ΔSO4–Se of 20‰), probably the result of SO2 disproportionation in or below the lake. The lake waters show strong enrichments in 18O and D relative to local meteoric waters, a result of the combined effects of mixing between isotopically heavy fluids of deep origin and meteoric water, and evaporation-induced fractionation at the lake surface. The stable-isotope systematics combined with energy-balance considerations support very rapid fluid cycling through the lake system. Lake levels and element concentrations show strong seasonal fluctuations, indicative of a short water residence time in the lake as well.Thermodynamic modeling of the lake fluids indicates that the lake water is saturated with silica phases, barite, pyrite and various Pb, Sb, Cu, As, Bi-bearing sulfides when sulfur saturation is assumed. Precipitating phases predicted by the model calculations are consistent with the bulk chemistry of the sulfur-rich bottom sediments and their identified mineral phases. Much of the lake water chemistry can be explained by congruent rock dissolution in combination with preferential enrichments from entering fumarolic gases or brines and element removal by precipitating mineral phases, as indicated by a comparison of the fluids, volcanic rocks and lake bed sediment.Flank springs on the mountain at different elevations vary in composition, and are consistent with local rock dissolution as a dominant factor and pH-dependent element mobility. Discharges of warm sulfate- and chloride-rich water at the highest elevation and a near-neutral spring at lower level may contain a small contribution of crater-lake water. The acid fluid-induced processes at Patuha have led to the accumulation of elements that are commonly associated with volcano-hosted epithermal ore deposits. The dispersal of heavy metals and other potentially toxic elements from the volcano via the local drainage system is a matter of serious environmental concern.  相似文献   

13.
Sulfur isotope effects during the SO2 disproportionation reaction to form elemental sulfur (3SO2+3H2O→2HSO4−+S+2H+) at 200–330°C and saturated water vapor pressures were experimentally determined. Initially, a large kinetic isotopic fractionation takes place between HSO4− and S, followed by a slow approach to equilibrium. The equilibrium fractionation factors, estimated from the longest run results, are expressed by 1000 ln αHSO4−–S=6.21×106/T2+3.62. The rates at which the initial kinetic fractionation factors approach the equilibrium ones were evaluated at the experimental conditions.δ34S values of HSO4− and elemental sulfur were examined for active crater lakes including Noboribetsu and Niseko, (Hokkaido, Japan), Khloridnoe, Bannoe and Maly Semiachik (Kamchatka), Poás (Costa Rica), Ruapehu (New Zealand) and Kawah Ijen and Keli Mutu (Indonesia). ΔHSO4−–S values are 28‰ for Keli Mutu, 26‰ for Kawah Ijen, 24‰ for Ruapehu, 23‰ for Poás, 22‰ for Maly Semiachik, 21‰ for Yugama, 13‰ for Bannoe, 9‰ for Niseko, 4‰ for Khloridonoe, and 0‰ for Noboribetsu, in the decreasing order. The SO2 disproportionation reaction in the magmatic hydrothermal system below crater lakes where magmatic gases condense is responsible for high ΔHSO4−–S values, whereas contribution of HSO4− produced through bacterial oxidation of reduced sulfur becomes progressively dominant for lakes with lower ΔHSO4−–S values. Currently, Noboribetsu crater lake contains no HSO4− of magmatic origin. A 40-year period observation of δ34SHSO4− and δ34SS values at Yugama indicated that the isotopic variations reflect changes in the supply rate of SO2 to the magmatic hydrothermal system. This implies a possibility of volcano monitoring by continuous observation of δ34SHSO4− values. The δ18O values of HSO4− and lake water from the studied lakes covary, indicating oxygen isotopic equilibration between them. The covariance gives strong evidence that lake water circulates through the sublimnic zone at temperatures of 140±30°C.  相似文献   

14.
δ87Sr values and Ca/Sr ratios were employed to quantify solute inputs from atmospheric and lithogenic sources to a catchment in NW Germany. The aquifer consists primarily of unconsolidated Pleistocene eolian and fluviatile deposits predominated by >90% quartz sand. Accessory minerals include feldspar, glauconite, and mica, as well as disperse calcium carbonate in deeper levels. Decalcification of near-surface sediment induces groundwater pH values up to 4.4 that lead to enhanced silicate weathering. Consequently, low mineralized Ca–Na–Cl- and Ca–Cl-groundwater types are common in shallow depths, while in deeper located calcareous sediment Ca–HCO3-type groundwater prevails. δ87Sr values and Ca/Sr ratios of the dissolved pool range from 7.3 to −2.6 and 88 to 493, respectively. Positive δ87Sr values and low Ca/Sr ratios indicate enhanced feldspar dissolution in shallow depths of less than 20 m below soil surface (BSS), while equilibrium with calcite governs negative δ87Sr values and elevated Ca/Sr ratios in deep groundwater (>30 m BSS). Both positive and negative δ87Sr values are evolved in intermediate depths (20–30 m BSS). For groundwater that is undersaturated with respect to calcite, atmospheric supplies range from 4% to 20%, while feldspar-weathering accounts for 8–26% and calcium carbonate for 62–90% of dissolved Sr2+. In contrast, more than 95% of Sr2+ is derived by calcium carbonate and less than 5% by feldspar dissolution in Ca–HCO3-type groundwater. The surprisingly high content of carbonate-derived Sr2+ in groundwater of the decalcified portion of the aquifer may account for considerable contributions from Ca-containing fertilizers. Complementary tritium analyses show that equilibrium with calcite is restricted to old groundwater sources.  相似文献   

15.
We have used in-situ pumps which filter large volumes of sea water through a 1 μm cartridge prefilter and two MnO2-coated cartridges to obtain information on dissolved and particulate radionuclide distributions in the oceans. Two sites in the northwest Atlantic show subsurface maxima of the fallout radionuclides137Cs,239,240Pu and241Am. Although the processes of scavenging onto sinking particles and release at depth may contribute to the tracer distributions, comparison of predicted and measured water column inventories suggests that at least 35–50% of the Pu and241Am are supplied to the deep water by advection.The depth distributions of the naturally occurring radionuclides232Th,228Th and230Th reflect their sources to the oceans.232Th shows high dissolved concentrations in surface waters, presumably as a result of atmospheric or riverine supply. Activities of232Th decrease with depth to values 0.01 dpm/1000 l.228Th shows high activities in near surface and near bottom water, due to the distribution of its parent,228Ra. Dissolved230Th, produced throughout the water column from234U decay, increases with depth to 3000 m. Values in the deep water (> 3000 m) are nearly constant ( 0.6–0.7 dpm/1000 l), and the distribution of this tracer (and perhaps other long-lived particle-reactive tracers as well) may be affected by the advection inferred from Pu and241Am data.The ratio of particulate to dissolved activity for both230Th and228Th is 0.15–0.20. This similarity precludes the calculation of sorption rate constants using a simple model of reversible sorption equilibrium. Moreover, in mid-depths228Th tends to have a higher particulate/dissolved ratio than230Th, suggesting uptake and release of230Th and228Th by different processes. This could occur if228Th, produced in surface water, were incorporated into biogenic particles formed there and released as those particles dissolved or decomposed during sinking.230Th, produced throughout the water column, may more closely approach a sorption equilibrium at all depths.230Th,241Am and239,240Pu are partitioned onto particles in the sequence Th > Am > Pu with 15% of the230Th on particles compared with 7% for Am and 1% for Pu. Distribution coefficients (Kd) are 1.3–1.6 × 107 for Th, 5–6 × 106 for Am and 7–10 × 105 for Pu. The lower reactivity for Pu is consistent with analyses of Pu oxidation states which show 85% oxidized (V + VI) Pu. However, theKd value for Pu may be an upper limit because Pu, like228Th, may be incorporated into particles in surface waters and released at depth only by destruction of the carrier phase.  相似文献   

16.
Mean dissolved inorganic nitrogen concentrations ([DIN]) in deep, seasonally stratified lakes with comparable DIN inputs can differ by up to a factor of 3 depending on hydraulic and morphometric properties and/or different trophic states of the lakes. In such lakes, net N sedimentation rates were estimated with two independent methods (sediment core analysis and input-output mass balances). They were higher in eutrophic lakes (Mean: 5.1; SD: ± 1.6 g m–2 yr–1; n = 13) than in oligotrophic lakes (1.6 ± 1.0 g m–2 yr–1; n = 3), but independent of [DIN]. Gaseous N loss rates to the atmosphere, as calculated from combined N- and P-mass balances from selected lakes, ranged from 0.9 to 37.4 g m–2 yr–1 (n = 10) and were positively correlated with [DIN]. Reduction of NO 3 - to N2 is assumed to be the main cause for gaseous N losses. A simple one-box mass balance model for [DIN], based on DIN input and rates and kinetics of N removal processes (net sedimentation and gaseous N loss) is proposed, and validated with a data base on [DIN] and DIN input in 19 deep, seasonally stratified lakes of central Europe. The model illustrated that the amount of water loading per unit surface area of a lake (called water discharge height q) is the critical parameter determining mean lake [DIN] relative to mean input [DIN]. Lakes with a q > 50 m yr–1 have average [DIN] similar to the [DIN] of the inflows regardless of their trophic states, because input and outflow exceed lake-internal N removal processes. A high primary production favors DIN removal in lakes with q < 50 m yr–1. It is concluded that measures to decrease primary production, e.g. by means of P removal programs, lead to an increase of [DIN] in lakes.  相似文献   

17.
Data of hydrological and hydrochemical observations conducted in August 2000 at Lake Seliger and its major tributaries are presented. The analyzed characteristics included: O2, H2S, CH4, microelements; mineral and organic compounds of P and N, ionic composition components (HCO3 –, Cl–, Na+, K+, dry residue, pH; color index, electrical conductivity. Bottom sediment samples were analyzed for microelement concentrations, CH4, oil hydrocarbons. The influence of the basin on the ecological state of the lake was assessed, and tendencies in the evolution of its ecosystem are analyzed. It is shown that the ecological conditions of the lake has not changed significantly since 1960–1991, however, nutrient concentrations in the lake water was found to increase.  相似文献   

18.
Thermal springs of the Boundary Creek hydrothermal system in the southwestern part of Yellowstone Park outside the caldera boundary vary in chemical and isotopic composition, and temperature. The diversity may be accounted for by a combination of processes including boiling of a deep thermal water, mixing of the deep thermal water with cool meteoric water and/or with condensed steam or steam-heated meteoric water, and chemical reactions with surrounding rocks. Dissolved-silica, Na+, K+ and Ca2+ contents of the thermal springs could result from a thermal fluid with a temperature of 200 ± 20°C. Chloride-enthalpy and silica-enthalpy mixing models suggest mixing of 230°C, 220 mg/l Cl− thermal water with cool, low-Cl− components. A 350 to 390°C component with Cl− ≥ 300 mg/l is possibly present in thermal springs inside the caldera but is not required to fit observed spring chemical and isotopic compositions. Irreversible mass transfer models in which a low-temperature water reacts with volcanic glass as it percolates downward and warms, can account for observed pH and dissolved-silica, K+, Na+, Ca2+ and Mg2+ concentrations, but produces insufficient Cl− or F− for measured concentrations in the warm springs. The ratio of aNa/aH, and Cl− are best accounted for in mixing models. The water-rock interaction model fits compositions of acid-sulfate waters observed at Summit Lake and of low-Cl− waters involved in mixing.The cold waters collected from southwestern Yellowstone Park have δD values ranging from −118 to −145 per mil and δ18O values of −15.9 to −19.4 per mil. Two samples from nearby Island Park have δD values of −112 and −114 per mil and δ18O values of −15.1 and −15.3 per mil. All samples of thermal water plot significantly to the right of the meteoric water line. The low Cl− and variable δD values of the thermal waters indicate isotopic compositions are derived by extensive dilution with cold meteoric water and by steam separation on ascent to the surface. Many of the hot springs with higher δD values may contain in addition a significant amount of high-D, low-Cl−, acid-sulfate or steam-heated meteoric water. Mixing models, Cl− content and isotopic compositions of thermal springs suggest that 30% or less of a deep thermal component is present. For example, the highest-temperature springs from Three Rivers, Silver Scarf and Upper Boundary Creek thermal areas contain up to 70% cool meteoric water and 30% hot water components, springs at Summit Lake and Middle Boundary Creek spring 57 are acid-sulfate or steam-heated meteoric water; springs 27 and 48 from Middle Boundary Creek and 49 from Mountain Ash contain in excess of 50% acid-sulfate water; and Three Rivers spring 46 and Phillips could result from mixing hot water with 55% cool meteoric water followed by mixing of acid-sulfate water. Extensive dilution by cool meteoric water increases the uncertainties in quantity and nature of the deep meteoric, thermal component.  相似文献   

19.
Physical, chemical and isotopic parameters were measured in fumaroles at the Vulcano crater and in drowned fumaroles near the beach. The data were used to define boundary conditions for possible conceptual models of the system.Crater fumaroles: time variations of CO2 and SO2 concentrations indicate mixing of saline gas-rich water with local fresh water. Cl/Br ratios of 300– 400 favour sea-water as a major source for Cl, Brand part of the water in the fumaroles. Cl concentrations and D values revealed, independently, amixing of 0.75 sea-water with 0.25 local freshwaterin furmarole F-5 during September 1982.Patterns of parameter correlation and mass balances reveal that CO2, S, NH3 and B originate from sources other than sea water. The CO2 value of 13C = – 2%o favours, at least partial, origin from decomposition of sedimentary rocks rather than mantle-derived material. Radiogenic4He(1.3 × lO–3 ccSTP/g water) and radiogenic40Ar(10.6 × 10–4 ccSTP/g water) are observed, (4He/40Ar)radiogenic = 1.2, well in the range of values observed in geothermal systems.Drowned fumaroles: strongly bubbling gas at a pond and at the beachappears to have the same origin and initial compositionas the crater fumaroles (2 km away). The fumarolic gas is modified by depletion of the reactive gases, caused by dissolution in shallow-water. Atmospheric Ne, Ar, Kr and Xe are addeden route, some radiogenic He and Ar are maintained. The Vulcano system seems to be strongly influenced by the contribution of sea-water and decomposition of sedimentary rocks. Evidence of magmatic contributions is mainly derived from heat.  相似文献   

20.
Load relaxation and cross-head displacement rate-change experiments have been used to establish log10 stress intensity factor (K) versus log10 crack velocity (v) diagrams for double torsion specimens, of synthetic quartz cracked on thea plane in liquid water and moist air.For crack propagation normal toz and normal tor at 20°C,K Ic (the critical stress intensity factor) was found to be 0.852±0.045 MN·m–3/2 and 1.002±0.048 MN·m–3/2, respectively.Subcritical crack growth at velocities from 10–3 m·s–1 to 10–9 m·s–1 at temperatures from 20°C to 80°C is believed to be facilitated by chemical reaction between the siloxane bonds of the quartz and the water or water vapour of the environment (stress corrosion). The slopes, of isotherms in theK-v diagrams are dependent upon crystallographic orientation. The isotherms have a slope of 12±0.6 for cracking normal tor and 19.9±1.7 for cracking normal toz. The activation enthalpy for crack propagation in the former orientation in liquid water at temperatures from 20°C to 80°C is 52.5±3.8 kJ·mole–1.A discussion is presented of the characteristics of theK-v diagrams for quartz.  相似文献   

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