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1.
In sediments with oxidized surface layers, the percentage of mineralized nitrogen that is nitrified/denitrified, compared with that released directly as ammonium, appears to be affected by the presence of sea salts. In estuarine systems, a significant portion of the nitrogen is released as ammonium, whereas in freshwater systems, most of the mineralized nitrogen is often released from the sediments as nitrogen gas. We hypothesized that this discrepancy is caused by differential competition between physical diffusion and nitrification/denitrification in the two systems. The vertical migration (by Fickian diffusion) of ammonium out of the oxic layer may be hindered by cation exchange (or sorption) interactions with sediment particles to a greater extent in fresh water than in estuarine systems. The resulting relatively long residence time, and potentially high levels of particle-bound ammonium in the freshwater sediments, would favor nitrification as the major ammonium removal process. By contrast, ion pair formation of ammonium with seawater anions and blockage of sediment cation exchange sites with seawater cations may allow a sizable fraction of the ammonium to diffuse out of estuarine sediments before it is nitrified. A salt effect, consistent with this hypothesis, has been demonstrated in experimental systems by changing the ionic composition of water flowing above intact cores of freshwater and estuarine sediments. Steady-state ammonium release from Lake Michigan sediments was substantially enhanced in the presence of 30% seawater over that in the presence of lake water alone. Likewise, steady-state ammonium release, from Ochlockonee River and Bay sediments (Florida) and from Toms River and Barnegat Bay sediments (New Jersey), was usually higher in the presence of diluted synthetic seawater than it was in the presence of fresh water.  相似文献   

2.
The release of exchangeable Mg in marine sediments from displacement by ammonium ions was estimated by way of experimentally determining the parameters that govern this ion-exchange equilibrium on solid geochemical phases: smectite, humic acid, illite and opal.

We showed that: (a) both the conditional selectivity constant as well as the solid concentration are important parameters in determining the relative contribution of ammonium-exchangeable Mg from smectite, organic matter, illite and opal; and (b) that, except in the cases where opal or organic matter concentrations are very high, the clays are the dominant carrier phases for labile Mg which is exchangeable by ammonium.

A model, based on the sum of the contributions from the major geochemical phases present in the sediment reliably predicts the amount of Mg released by exchange with ammonium in marine sediments.  相似文献   


3.
In Carboniferous shales a relationship has been found between exchangeable cations and palaeosalinity. In the marine shales the concentration of exchangeable Mg is higher than in shales deposited in fresh and brackish water, and the concentrations of exchangeable Ca, Na and K are lower. The same relationships have been observed in modern sediments. When the cation concentrations in the whole rock are compared with the exchangeable cation concentrations, incorporation into the sediment of K and possibly Mg in the marine environment is indicated. Furthermore, the loss of Ca and Na from the sediment can be accounted for by the loss from exchange sites. Reactions taking place during halmyrolysis would appear to be more important than those taking place during diagenesis.  相似文献   

4.
The complex lithological, geochemical, geochronological, and micropaleontological (diatoms, spores, pollen) investigations of stratified bottom sediments that constitute facies-variable sedimentary sequences in a small isolated lake located near the upper limit of the sea on the White Sea coast made it possible to define lithostratigraphic units (LSU) forming the complete sedimentary succession in deep parts of isolated basins. It is shown that stratigraphy of heterogeneous sequences is determined by two regional transgressive–regressive cycles in relative sea level fluctuations: alternating late Glacial and Holocene transgressions and regressions. The lower part of a clastogenic clayey–sandy–silty sequence successively composed of freshwater (LSU 1) and brackish-water (LSU 2) sediments of the ice-marginal basins and marine postglacial facies (LSU 3) was formed during the late Glacial glacioeustatic marine transgression. Its upper part formed in different isolated basins at different stages of the Holocene is represented depending on its altimetric position on the coastal slope by costal marine sediments (LSU 4) and facies of the partly isolated inlet (LSU 5). The organogenic sapropelic sequence, which overlies sediments of the marine basin and partly isolated bay, corresponds to lithostratigraphic units represented by Holocene sediments accumulated in the meromictic lake (LSU 6), onshore freshwater basin (LSU 7), and freshwater basin with elevated water mineralization (LSU 8) deposited during maximum development of Holocene transgression and lacustrine sediments (LSU 9) formed in coastal environments during terminal phases of the Holocene. The defined lithostratigraphic units differ from each other in lithological, micropaleontological, and geochemical features reflected in structural and textural properties of their sediments, their composition, inclusions, and composition of paleophytocoenoses and diatom assemblages.  相似文献   

5.
选取贵州百花湖入湖支流麦西河为对象,研究了上覆水—孔隙水—沉积物体系氮的形态差异,结果表明:麦西河上覆水中,以硝态氮(NO-3-N)为主,氨态氮(NH+4-N)次之,亚硝态氮(NO-2-N)最低;孔隙水中,溶解无机氮中以NH+4-N为主, NO-3-N次之, NO-2-N最低;沉积物中,总氮(TN)的含量为1110.67～4413.16mg/kg;固定态铵含量为34.56～170.05mg/kg,占TN的1.47%～6.25%;可交换态氮以NH+4-N为主, NO-3-N次之, NO-2-N最低。孔隙水NH+4-N是上覆水NH+4-N的2.65～19.51倍,上覆水NO-3-N是孔隙水NO-3-N的7.14～20.43倍。沉积物TN与孔隙溶解水无机氮(DIN)、孔隙水NH+4-N、沉积物可交换态氮和沉积物可交换性NH+4-N呈显著正相关;在沉积物中,可交换性NO-3-N与可交换性NH+4-N及可交换态氮呈显著正相关,可交换性NH+4-N与可交换态氮呈极显著正相关;孔隙水溶解无机氮与孔隙水NH+4-N呈极显著正相关。麦西河不同介质中氮的迁移关系则表现为:由于浓度梯度,上覆水中的NO-3-N扩散到孔隙水中,进而累积到沉积物中;沉积物的可交换性NH+4-N,进入孔隙水,最终扩散到上覆水中。   相似文献   

6.
Total organic nitrogen (TON) and phosphorus (TOP) were measured as a function of depth in 14 cores taken from a New England, tidal, freshwater marsh. TON and TOP ranged from 1.56 to 1.97% and 0.11 to 0.30% of dry weight sediments, respectively. The variation in both pool sizes over time was small and TON varied inconsistently with depth; however, TOP decreased regularly down to 20 cm. Consequently, the TON: TOP ratio increased linearly from 14∶1 at the surface to 32∶1 at 20 cm, then was nearly constant to 70 cm. This pattern may be a general feature of marsh sediments and may indicate 1) that phosphorus is recycled less efficiently than nitrogen, 2) that over time proportionately more introgen than phosphorus is incorporated into recalcitrant compounds, or 3) that phosphorus is more mobile than nitrogen in these marsh sediments. The total inorganic nitrogen pool was measured in this marsh also and was dominated by ammonium (97% of total). The annual average free ammonium concentration was 3.70±0.64 mg N per 1 at the surface and decreased to 0.92±0.18 mg N per 1 at 20 to 22 cm in the sediments. Sorptiondesorption studies showed that, on a fresh sediment volume basis, sediment sorbed ammonium was roughly equivalent to free porewater ammonium (K=0.8). The relationship between free and sorbed ammonium was linear between 0.4 and 24.0 mg NH4·N per 1 of pore water. The depth distribution of ammonium in these sediments is probably maintained by a dynamic balance between net microbial mineralization of litter, plant uptake, transpiration, diffusion, and porewater advection.  相似文献   

7.
Analyses of organic carbon, total nitrogen, and inorganically bound ammonium (exchangeable and fixed ammonium) in two oxic deep-sea sediment cores from the Central Pacific Ocean revealed insufficiently high inorganic ammonium contents of these sediments to explain the low C/N ratios, although representing 20–45% of the total nitrogen.Both, organic carbon/total nitrogen ratios (ranging from 3.9?1.3) and organic carbon/organic nitrogen ratios (5.6?1.9) decrease with increasing sediment depth, the latter indicating a real enrichment of organic nitrogen compounds during diagenesis relative to total organic matter.Organic matter/alumina relationships indicate that this unusual preservation of organic nitrogen compounds is probably caused by sorption to clay minerals protecting them against bacterial attack.  相似文献   

8.
The Khorat Plateau on the Indochina Terrane is known to have formed during the closure of the Tethys Ocean, although the origin of its potash mineral deposits is a topic of current debate. Data from a borehole on Savannakhet Basin is used in this study to re-define the evaporation processes of the study area. Geochemical analyses of halite from various borehole-derived evaporite strata have elucidated the fluid sources from which these ores formed. Measured δ11 B indicated that ore deposits formed primarily due to evaporation of seawater, although non-marine fluids affected the later stages of the evaporation process. Fluctuations in B and Br concentrations in carnallite-and sylvite-rich strata indicate the influence of fresh water. Boron concentration in carnallite unit indicated the influence of hydrothermal fluids. From the relative timings of these various fluid influxes, the evolution of these evaporates can be divided into four stages:(1) an initial marine evaporation at the beginning of the deposit's formation, where seawater(and minor fresh water) trapped on the uplifted Khorat Plateau produced sediments and salts with Br contents lower than those of normal marine-derived evaporites;(2) a transgression stage, where seawater recharged the basin;(3) a hydrothermal infiltration stage, which was coeval with the late Yanshan movement; and(4) a stage of fresh water supply, as recorded by fluctuations in B and Br contents, inferring intermittent fresh water influx into the basin. Thus, although evaporites on the Savannakhet Basin primarily formed via marine evaporation, they were also influenced to a significant degree by the addition of non–marine fresh water and hydrothermal fluids.  相似文献   

9.
《Applied Geochemistry》2005,20(2):295-316
A confined aquifer system has developed in argillaceous marine and freshwater sediments of Pliocene–Holocene age in the northeastern Osaka Basin (NEOB) in central Japan. The shallow groundwater (<100 m) in the system is recharged in a northern hilly to mountainous area with dominantly Ca-HCO3 type water, which changes as it flows toward the SW to Mg-HCO3 type and then to Na-HCO3 type water. Comparison of the chemical and Sr isotopic compositions of the groundwater with those of the bulk and exchangeable components of the underground sediments indicates that elements leached from the sediments contribute negligibly to the NEOB aquifer system. Moreover, model calculations show that contributions of paleo-seawater in the deep horizon and of river water at the surface are not major factors of chemical change of the groundwater. Instead, the zonal pattern of the HCO3-dominant groundwater is caused by the loss of Ca2+ from the water as it is exchanged for Mg2+ in clays, followed by loss of Mg + Ca as they are exchanged for Na + K in clays between the Ca-HCO3 type recharge water and the exchangeable cations in the clay layers, which were initially enriched in Na+. Part of this process was reproduced in a chromatographic experiment in which Na type water with high 87Sr/86Sr was obtained from Mg type water with low 87Sr/86Sr by passing it through marine clay packed in a column. The flux of recharge water into the confined aquifer system according to this chromatographic model is estimated to be 0.99 mm/day, which is compatible with the average recharge flux to unconfined groundwater in Japan (1 mm/day).  相似文献   

10.
A radiotracer technique, employing 27Mg, is used to determine the Mg released by ammonium exchange on undis-solved humic acid in a seawater medium. This new method allows for the measurement of exchangeable Mg on the solid phase surface, which eliminates the problem caused by the high-Mg background in the seawater matrix. The precision calculated from the counting statistics is better than ±2%; the reproducibility among repeated counts ranged from ±1% to ±3%. The higher sensitivity of the method allows for monitoring the Mg---NH4 exchange at concentrations as low as 30 mM NH4. This is a major improvement relative to the data obtained with the analytical methods used so far, which allow detection of exchangeable Mg only at NH4 concentrations higher than 1 M. The lower experimental concentrations are more in accordance with the natural ammonium levels found in anoxic marine sediments. For the undissolved humic acid used in this experiment, the amount of exchangeable Mg in apparent equilibrium with an ammonium-free seawater matrix was found to be 96.6 ± 0.4 meq/100g. The Mg---NH4 exchange on humic acid in seawater comes to a steady-state value in < 18 min. The conditional equilibrium constant obtained for this reaction, Kcond = 0.039 ± 0.001 M−1. The technique can be expanded to other geochemical solid phases in seawater and it can be modified to study the behavior of the major cations by using 24Na, 42K and 49Ca.  相似文献   

11.
Extracellular enzymatic hydrolysis of high-molecular weight organic matter is the initial step in sedimentary organic carbon degradation and is often regarded as the rate-limiting step. Temperature effects on enzyme activities may therefore exert an indirect control on carbon mineralization. We explored the temperature sensitivity of enzymatic hydrolysis and its connection to subsequent steps in anoxic organic carbon degradation in long-term incubations of sediments from the Arctic and the North Sea. These sediments were incubated under anaerobic conditions for 24 months at temperatures of 0, 10, and 20 °C. The short-term temperature response of the active microbial community was tested in temperature gradient block incubations. The temperature optimum of extracellular enzymatic hydrolysis, as measured with a polysaccharide (chondroitin sulfate), differed between Arctic and temperate habitats by about 8-13 °C in fresh sediments and in sediments incubated for 24 months. In both Arctic and temperate sediments, the temperature response of chondroitin sulfate hydrolysis was initially similar to that of sulfate reduction. After 24 months, however, hydrolysis outpaced sulfate reduction rates, as demonstrated by increased concentrations of dissolved organic carbon (DOC) and total dissolved carbohydrates. This effect was stronger at higher incubation temperatures, particularly in the Arctic sediments. In all experiments, concentrations of volatile fatty acids (VFA) were low, indicating tight coupling between VFA production and consumption. Together, these data indicate that long-term incubation at elevated temperatures led to increased decoupling of hydrolytic DOC production relative to fermentation. Temperature increases in marine sedimentary environments may thus significantly affect the downstream carbon mineralization and lead to the increased formation of refractory DOC.  相似文献   

12.
The characteristics of nitrogen fractions in the surface sediments of lakes from Eastern Plain Region, Yunnan-Guizhou Plateau Region, Northeast China Region, Qinghai-Tibet Plateau Region and Mongolia-Xinjiang Plateau Region were investigated and the differences of five lake regions on nitrogen fractionation were discussed. The results indicated that organic nitrogen (Norg) was the major nitrogen fraction accounting for 76.38–92.02 % of Ntot in sediments. The rank order of average Norg and Ntot of sediments in five lake regions was: Yunnan-Guizhou Plateau Region > Northeast China Region > Mongolia-Xinjiang Plateau Region > Qinghai-Tibet Plateau Region > Eastern Plain Region. The exchangeable nitrogen had a similar distribution as organic nitrogen in the studied sediments. NH4 +–N is the main exchangeable nitrogen of sediments in the studied lakes except in Lake Qinghai and Lake Yamdrok which contained higher nitrate concentrations than ammonium. Fixed ammonium (Nfix) in the sediments of studied lakes was irregularly distributed with the values ranging from 99.45 to 329.02 mg/kg. TOC was significantly and positively correlated with ammonium, nitrate, Norg and Ntot, while Nfix was negatively correlated with nitrate probably due to electrostatic attraction between Nfix and nitrate in layers of sediments.  相似文献   

13.
《Applied Geochemistry》1999,14(1):41-52
Concentrations of S, organic C and Fe were investigated in profiles of sediments from two estuarine systems in the SW of Western Australia. In marine-affected sediments, inorganic S dominates total S and concentrations of total S correlate with Fe and not with organic C. In freshwater sediments, organic S dominates total S and concentrations of total S correlate with organic C and not with Fe. Molar Fe/S ratios in the estuarine sediments decrease with increasing salinity and approach unity for marine conditions. Net accumulation rates of S in sediments were estimated with a numerical computer model, calibrated with published data on profiles of marine sediments for diffusion of SO2−4, sedimentation rates and distributions of S. Measured depth-integrated reduction rates of SO2−4 in the marine-affected estuarine sediments approach those obtained for Fe-limited marine conditions at similar rates of sedimentation. Measured concentrations of inorganic S in anoxic freshwater sediments fit a numerically calculated relationship between inorganic S and sedimentation rate.  相似文献   

14.
Carbonate concretions, lenses and bands in the Pleistocene, Palaeogene and Upper Triassic coalfields of Japan consist of various carbonate minerals with varied chemical compositions. Authigenic carbonates in freshwater sediments are siderite > calcite > ankerite > dolomite >> ferroan magnesite; in brackish water to marine sediments in the coal measures, calcite > dolomite > ankerite > siderite >> ferroan magnesite; and in the overlying marine deposits, calcite > dolomite >> siderite. Most carbonates were formed progressively during burial within a range of depths between the sediment-water interface and approximately 3 km. The mineral species and the chemical composition of the carbonates are controlled primarily by the initial sedimentary facies of the host sediments and secondarily by the diagenetic evolution of pore water during burial. Based on the regular sequence and burial depth of precipitation of authigenic carbonates in a specific sedimentary facies, three diagenetic stages of carbonates are proposed. Carbonates formed during Stage I (< 500 m) strongly reflect the initial sedimentary facies, e.g. low Ca-Mg siderite in freshwater sediments which are initially rich in iron derived from lateritic soil on the nearby landmass, and Mg calcite and dolomite in brackish-marine sediments whose pore waters abound in Ca2+ and Mg2+ originating in seawater and calcareous shells. Carbonates formed during Stage II (500–2000 m) include high Ca-Mg siderite, ankerite, Fe dolomite and Fe–Mg calcite in freshwater sediments. The assemblage of Stage II carbonates in brackish-marine sediments in the coal measures is similar to that in freshwater sediments. This suggests similar diagenetic environments owing to an effective migration and mixing of pore water due to the compaction of host sediments. Carbonates formed during Stage III (> 2000 m) are Fe calcite and extremely high Ca-Mg siderite; the latter is exclusively in marine mudstones. The supply of Ca is partly from the alteration of silicates in the sediments at elevated burial temperatures. After uplift, calcite with low Mg content precipitates from percolating groundwater and fills extensional cracks.  相似文献   

15.
We examined the effects of seasonal salinity changes on sediment ammonium (NH4 +) adsorption and exchange across the sediment–water interface in the Parker River Estuary, by means of seasonal field sampling, laboratory adsorption experiments, and modeling. The fraction of dissolved NH4 + relative to adsorbed NH4 + in oligohaline sediments rose significantly with increased pore water salinity over the season. Laboratory experiments demonstrated that small (∼3) increases in salinity from freshwater conditions had the greatest effect on NH4 + adsorption by reducing the exchangeable pool from 69% to 14% of the total NH4 + in the upper estuary sediments that experience large (0–20) seasonal salinity shifts. NH4 + dynamics did not appear to be significantly affected by salinity in sediments of the lower estuary where salinities under 10 were not measured. We further assessed the importance of salinity-mediated desorption by constructing a simple mechanistic numerical model for pore water chloride and NH4 + diffusion for sediments of the upper estuary. The model predicted pore water salinity and NH4 + profiles that fit measured profiles very well and described a seasonal pattern of NH4 + flux from the sediment that was significantly affected by salinity. The model demonstrated that changes in salinity on several timescales (tidally, seasonally, and annually) can significantly alter the magnitude and timing of NH4 + release from the sediments. Salinity-mediated desorption and fluxes of NH4 + from sediments in the upper estuary can be of similar magnitude to rates of organic nitrogen mineralization and may therefore be important in supporting estuarine productivity when watershed inputs of N are low.  相似文献   

16.
Since 1991, Mississippi River water has been diverted at Caernarvon, Louisiana, into Breton Sound estuary. Breton Sound estuary encompasses 1100 km2 of fresh and brackish, rapidly subsiding wetlands. Nitrite + nitrate, total Kjeldahl nitrogen, ammonium, total phosphorus, total suspended sediments, and salinity concentrations were monitored at seven locations in Breton Sound from 1988 to 1994. Statistical analysis of the data indicated decreased total Kjeldahl nitrogen with associated decrease in total nitrogen, and decreased salinity concentrations in the estuary due to the diversion. Spring and summer water quality transects indicated rapid reduction of nitrite + nitrate and total suspended sediment concentration as diverted Mississippi River water entered the estuary, suggesting near complete assimilation of these constituents by the ecosystem. Loading rates of nitrite + nitrate (5.6–13.4 g m−2 yr−1), total nitrogen (8.9–23.4 g m−2 yr−1), and total phosphorus (0.9–2.0 g m−2 yr−1) were calculated along with removal efficiencies for these constituents (nitrite + nitrate 88–97%; total nitrogen 32–57%; total phosphorus 0–46%). The low impact of the diversion on water quality in the Breton Sound estuary, along with assimilation of TSS over a very short distance, suggests that more water may be introduced into the estuary without detrimental affects. This would be necessary if freshwater diversions are to be used to distribute nitrients and sediments into the lower reaches of the estuary, in an effort to compensate for relative sea-level rise, and reverse the current trend of rapid loss of wetlands in coastal Louisiana.  相似文献   

17.
Subterranean estuary occupies the transition zone between hypoxic fresh groundwater and oxic seawater, and between terrestrial and marine sediment deposits. Consequently, we hypothesize, in a subterranean estuary, biogeochemical reactions of Fe respond to submarine groundwater discharge (SGD) and sea level rise. Porewater and sediment samples were collected across a 30-m wide freshwater discharge zone of the Indian River Lagoon (Florida, USA) subterranean estuary, and at a site 250 m offshore. Porewater Fe concentrations range from 0.5 μM at the shoreline and 250 m offshore to about 286 μM at the freshwater-saltwater boundary. Sediment sulfur and porewater sulfide maxima occur in near-surface OC-rich black sediments of marine origin, and dissolved Fe maxima occur in underlying OC-poor orange sediments of terrestrial origin. Freshwater SGD flow rates decrease offshore from around 1 to 0.1 cm/day, while bioirrigation exchange deepens with distance from about 10 cm at the shoreline to about 40 cm at the freshwater-saltwater boundary. DOC concentrations increase from around 75 μM at the shoreline to as much as 700 μM at the freshwater-saltwater boundary as a result of labile marine carbon inputs from marine SGD. This labile DOC reduces Fe-oxides, which in conjunction with slow discharge of SGD at the boundary, allows dissolved Fe to accumulate. Upward advection of fresh SGD carries dissolved Fe from the Fe-oxide reduction zone to the sulfate reduction zone, where dissolved Fe precipitates as Fe-sulfides. Saturation models of Fe-sulfides indicate some fractions of these Fe-sulfides get dissolved near the sediment-water interface, where bioirrigation exchanges oxic surface water. The estimated dissolved Fe flux is approximately 0.84 μM Fe/day per meter of shoreline to lagoon surface waters. Accelerated sea level rise predictions are thus likely to increase the Fe flux to surface waters and local primary productivity, particularly along coastlines where groundwater discharges through sediments.  相似文献   

18.
Benthic metabolism and nutrient exchange across the sediment-water interface were examined over an annual cycle at four sites along a freshwater to marine transect in the Parker River-Plum Island Sound estuary in northeastern Massachusetts, U.S. Sediment organic carbon content was highest at the freshwater site (10.3%) and decreased along the salinity gradient to 0.2% in the sandy sediments at the marine end of the estuary. C:N ratios were highest in the mid estuary (23:1) and lowest near the sea (11:1). Chlorophyll a in the surface sediments was high along the entire length of the estuary (39–57 mg chlorophyll a m−2) but especially so in the sandy marine sediments (172 mg chlorophyll a m−2). Chlorophyll a to phaeophytin ratios suggested most chlorophyll is detrital, except at the sandy marine site. Porewater sulfide values varied seasonally and between sites, reflecting both changes in sulfate availability as overlying water salinity changed and sediment metabolism. Patterns of sediment redox potential followed those of sulfide. Porewater profiles of inorganic N and P reflected strong seasonal patterns in remineralization, accumulation, and release. Highest porewater NH4 + values were found in upper and mid estuarine sediments, occasionally exceeding 1 mM N. Porewater nitrate was frequently absent, except in the sandy marine sediments where concentrations of 8 μM were often observed. Annual average respiration was lowest at the marine site (13 mmol O2 m−2 d−1 and 21 mmol TCO2 m−2 d−1) and highest in the mid estuary (130 mmol O2 m−2 d−1 and 170 mmol TCO2 m−2 d−1) where clam densities were also high. N2O and CH4 fluxes were low at all stations throughout the year: Over the course, of a year, sediments varied from being sources to sinks of dissolved organic C and N, with the overall spatial pattern related closely to sediment organic content. There was little correlation between PO4 3− flux and metabolism, which we attribute to geochemical processes. At the two sites having the lowest salinities, PO4 3− flux was directed into the sediments. On average, between 22% and 32% of total system metabolism was attributable to the benthos. The mid estuary site was an exception, as benthic metabolism accounted for 95% of the total, which is attributable to high densities of filter-feeding clams. Benthic remineralization supplied from less than 1% to over 190% of the N requirements and 0% to 21% of the P requirements of primary producers in this system. Estimates of denitrification calculated from stoichiometry of C and N fluxes ranged from 0% for the upper and mid estuary site to 35% for the freshwater site to 100% of sediment organic N remineralization at the marine site. We hypothesize that low values in the upper and mid estuary are attributable to enhanced NH4 + fluxes during summer due to desorption of exchangeable ammonium from rising porewater salinity. NH4 + desorption during summer may be a mechanism that maintains high rates of pelagic primary production at a time of low inorganic N inputs from the watershed.  相似文献   

19.
The paper reviews data (acquired in 2007–2016) on aliphatic and polycyclic aromatic hydrocarbons in comparison with data on concentrations of lipids, Corg, and chlorophyll a in the water and bottom sediments the river–sea geochemical barrier (for the Northern Dvina, Ob, Yenisei, and Lena rivers). It was established that the concentrations of anthropogenic hydrocarbons decrease and these compounds precipitate like other organic compounds and particulate matter, where riverine and marine waters mix. Relatively pure water flows in the pelagic zones of seas. In spite of low temperatures in the Arctic, anthropogenic hydrocarbons transform so rapidly that natural compounds dominate in the water and bottom sediments: autochthonous in the seawater and allochthonous in the bottom sediments.  相似文献   

20.
We measured archaeal lipid distributions from globally distributed samples of freshwater, marine, and hypersaline suspended particulate matter. Cluster analysis of relative lipid distributions identified four distinct groups, including: (1) marine epipelagic (<100 m) waters, (2) marine mesopelagic (200-1500 m) and upwelling waters, (3) freshwater/estuarine waters, and (4) hypersaline waters. A pronounced difference in lipid composition patterns is the near absence of ring-containing glycerol dialkyl glycerol tetraethers (GDGTs) at high salinity. Different archaeal communities populate marine (mesophilic Crenarchaeota and Euryarchaeota), and hypersaline environments (halophilic Euryarchaeota) and community shifts can regulate differences in lipid patterns between marine and hypersaline waters. We propose that community changes within meosphilic marine Archaea also regulate the lipid patterns distinguishing epipelagic and mesopelagic/upwelling zones. Changes in the relative amounts of crenarchaeol and caldarchaeol and low relative abundances of ringed structures in surface waters differentiate lipids from the epipelagic and mesopelagic/upwelling waters. Patterns of lipids in mesopelagic (and upwelling) waters are similar to those expected of the ammonia-oxidizing Group I Crenarchaeota, with predominance of crenarchaeol and abundant cyclic GDGTs; non-metric multidimensional analysis (NMDS) shows this pattern is associated with high nitrate concentrations. In contrast, limited culture evidence indicates marine Group II Euryarchaeota may be capable of producing mainly caldarchaeol and some, but not all, of the ringed GDGTs and we suggest that these organisms, along with the Crenarchaeota, contribute to lipids in epipelagic marine waters. Calculated TEX86 temperatures in mesopelagic samples (reported here and in published data sets) are always much warmer than measured in situ temperatures. We propose lipids used in the temperature proxy derive from both Euryarchaeaota and Crenarchaeota, and observed values of TEX86 are subject to changes in their ecology as influenced by nutrient fluctuations or other perturbations. Applications of published core-top TEX86-SST correlations require that (1) the surface waters are always composed of similar communities with the same temperature response and (2) that deeper water GDGT production is not transported to the sediments. Our lipid distribution patterns demonstrate both surface-water archaeal community differences (which accompany greater nutrient influxes, shoaling of mesopelagic Crenarchaeota during upwelling periods, and possibly due to an influx of terrestrial Archaea), and changes in organic matter transport through the water column can affect the distribution of lipids recorded in sediments. We therefore suggest that reported temperature shifts in ancient applications indicate TEX86 lipids recorded not only temperature changes, but also changes in archaeal ecology, nutrient concentrations, and possibly oceanographic conditions.  相似文献   

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