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1.
With the aim of evaluating temporal changes in sedimentation and organic carbon (Corg) supplied over the last ~100 years, a sediment core was collected at Soledad Lagoon, a costal ecosystem surrounded by mangroves, located in the Cispatá Estuary (Caribbean coast of Colombia). The core sediments were characterized by low concentrations of calcium carbonate (0.2–2.9%), organic matter (3–8%), total nitrogen (0.11–0.38%), and total phosphorus (0.19–0.65 mg g−1). Fe and Al concentrations ranged from 4% to 5%, and Mn from 356 to 1,047 μg g−1. The 210Pb-derived sediment and mass accumulation rates were 1.54 ± 0.18 mm year−1 and 0.08 ± 0.01 g cm−2 year−1, respectively. The sediment core did not provide evidence of human impact, such as enhancement of primary production or nutrient enrichment, which may result from recent land uses changes or climate change. The Corg fluxes estimated for Soledad Lagoon core lay in the higher side of carbon fluxes to coastal ecosystems (314–409 g m−2 year−1) and the relatively high Corg preservation observed (~45%) indicate that these lagoon sediments has been a net and efficient sink of Corg during the last century, which corroborate the importance of mangrove areas as important sites for carbon burial and therefore, long-term sequestration of Corg.  相似文献   

2.
210Pb geochronologies of Cd, Cu, Hg, and Pb fluxes were obtained from the intertidal mudflat sediments of the coastal lagoons Chiricahueto, Estero de Urías, and Ohuira in the Mexican Pacific. The Cu and Hg sediment concentrations at the three lagoons fell within the ranges of 6–76 μg g−1 and 0.1 to 592 ng g−1, respectively; Chiricahueto and Estero de Urías sediments had comparable Cd and Pb concentrations within the ranges of 0.2–2.1 μg g−1 and 10–67 μg g−1, respectively; whereas in Ohuira lagoon, Cd concentrations were lower (0.1–0.5 μg g−1) and Pb concentrations were higher (115–180 μg g−1) than in the other lagoons. The metal fluxes (μg cm−2 y−1) for the three lagoons fell within the ranges of 0.02–0.15 for Cd, 0.7–6.0 for Cu, 0.001–0.045 for Hg, and 0.7–20 for Pb. The Hg pollution in Estero de Urías was attributed to the exhausts of the thermoelectric plant of Mazatlan and the metal enrichment in Chiricahueto and Ohuira was related to the agrochemical wastes from the croplands surrounding these lagoons.  相似文献   

3.
In southern California, USA, wildfires may be an important source of mercury (Hg) to local watersheds. Hg levels and Hg accumulation rates were investigated in dated sediment cores from two southern California lakes, Big Bear Lake and Crystal Lake, located approximately 40-km apart. Between 1895 and 2006, fires were routinely minimized or suppressed around Big Bear Lake, while fires regularly subsumed the forest surrounding Crystal Lake. Mean Hg concentrations and mean Hg accumulation rates were significantly higher in Crystal Lake sediments compared to Big Bear Lake sediments (Hg levels: Crystal Lake 220 ± 93 ng g−1, Big Bear Lake 92 ± 26 ng g−1; Hg accumulation: Crystal Lake 790 ± 1,200 μg m−2 year−1, Big Bear 240 ± 54 μg m−2 year−1). In Crystal Lake, the ratio between post-1965 and pre-1865 Hg concentrations was 1.1, and several spikes in Hg levels occurred between 1910 and 1985. Given the remote location of the lake, the proximity of fires, and the lack of point sources within the region, these results suggested wildfires (rather than industrial sources) were a continuous source of Hg to Crystal Lake over the last 150 years.  相似文献   

4.
To determine if toxaphene residues in edible fish tissue decreased after removal of contaminated sediments from an estuarine site in 1999, 51 composite samples representing six finfish species were collected in 2001 and analyzed using gas chromatography with electron capture and negative ion mass spectrometric detection. The grand mean total toxaphene residue concentration on a wet weight basis (ΣTOXwet) was 1,400 ± 3,500 ng g−1 (range: < 18 to 18,000 ng g−1) and was positively correlated with extractable lipid. On a lipid basis, the mean ΣTOXlip was 26 ± 33 μg g1, which decreased with increasing distance from the study site. Although benthically-oriented species, such as spot (Leiostomus xanthurus) and striped mullet (Mugil cephalus), exhibited higher mean ΣTOXwet than those of higher trophic level fish, mean ΣTOXlip were not significantly different among species. The grand mean ΣTOX for 2001 was 3.8 (wet) and 2.6 (lipid) times less than corresponding preremedial action (1997) concentrations, suggesting that bioavailable toxaphene residues in this system have been reduced. Forage species, such as croaker (Micropogonias undulatus), mullet, and spot, preferentially accumulate toxaphene residues in this system and may serve as vectors of organochlorine contaminants in the estuarine and coastal ocean food web.  相似文献   

5.
An assessment of coastal pollution was made on the basis of trace element concentrations (arsenic — As, mercury — Hg) in the Gulf of Mannar. The beachrock samples were collected along the coastal tracts between Rameswaram and Kanyakumari. The samples were dried and digested to determine the As and Hg using atomic absorption spectrophotometer (AAS-air-acetylene and nitrous oxide method). The As and Hg accumulation status of the beachrock was assessed using geo-accumulation index values (I geo). The accumulation of As and Hg in the beachrock ranges from 2.75 to 20.72 μg g−1 and from 0.06 to 0.31 μg g−1, respectively. The As and Hg concentrations in the beachrocks are compared with crustal average values and average of other region sediments. The possible source of the contamination is from atmospheric deposition and anthropogenic activities.  相似文献   

6.
Oyster and sediment samples collected from six sites in Galveston Bay from 1986 to 1998 were analyzed for polynuclear aromatic hydrocarbons (PAHs). Total concentrations of parent PAHs in oysters ranged from 20 ng g−1 at one site to 9,242 ng g−1 at another and varied randomly with no clear trend over the 13 year period at any site. Concentrations of alkylated PAHs, which are indications of petroleum contamination, varied from 20 to 80,000 ng g−1 in oysters and were in higher abundance than the parent PAHs, indicating that one source of the PAH contaminants in Galveston Bay was petroleum and petroleum products. Four to six ring parent PAHs, which are indicative of combustion source , were higher than those of 2–3 ring parent PAHs, suggesting incomplete combustion generated PAHs was another source of PAHs into Galveston Bay. Concentrations of parent PAHs in sediments ranged from 57 to 670 ng g−1 and were much lower than those in oysters. Sediments from one site had a high PAH concentration of 5,800 ng g−1. Comparison of the compositions and concentrations of PAHs between sediment and oysters suggests that oysters preferentially bioaccumulate four to six ring PAHs. PAH composition in sediments suggests that the sources of PAH pollution in Galveston Bay were predominantly pyrogenic, while petroleum related PAHs were secondary contributions into the Bay.  相似文献   

7.
Sulfide Inhibition of Nitrate Removal in Coastal Sediments   总被引：1，自引：0，他引：1  
Microbial nitrate (NO3−) removal via denitrification (DNF) at high sulfide (H2S) concentrations was compared in sediment from a coastal freshwater pond in a developed area that receives salt-water influx during storm events, and a saline pond proximal to an undeveloped estuary. Sediments were incubated with added SO42− (1,000 μg per gram dry weight basis (gdw)) to determine whether acid volatile sulfides (AVS) were formed. DNF in the sediments was measured with NO3–N (300 μg gdw−1) alone, and with NO3–N and H2S (1,000 μg S2− gdw−1). SO42− addition to the freshwater sediments resulted in AVS formation (970 ± 307 μg S gdw−1) similar to the wetland with no added SO42− (986 ± 156 μg S gdw−1). DNF rates measured with no added H2S were greater in the freshwater than the wetland site (10.6 ± 0.6 vs. 6.4 ± 0.1 μg N2O–N gdw−1 h−1, respectively). High H2S concentrations retained NH4–N in the undeveloped wetland and retained NO3–N in the developed freshwater site, suggesting that potential salt-water influx may reduce the ability of the freshwater sediments to remove NO3–N.  相似文献   

8.
Phosphatase activity was measured in sediments from tidal freshwater habitats adjacent to the Cooper River in South Carolina representing different stages of ecological succession. It was found that sediment (0–5 cm) acid phosphatase activity, alkaline phosphatase activity and phosphodiesterase activity increased with increasing successional stage and phytomass. Acid phosphatase activity in creased from 7.5±1.2 (±1 SD) in subtidal sediment from a shallow open water habitat without vegetation to 61.2±4.9 μmol g−1 hr−1 (μmol of p-nitrophenol released per gram of dry sediment per hour) in intertidal sediments colonized by emergent macrophytes, while alkaline phosphatase activity increased from 2.1±0.1 to 19.01±1.5 μmol g−1 hr−1. Phosphodiesterase activity increased from 1.8±0.1 to 20.2±2.0 μmol g−1 hr−1 along the same gradient. Acid phosphatase activity was highly correlated (R2=0.92, P<0.001) with the organic matter content of the sediment. A study of phosphatase kinetics showed that Vmax of all phosphatases also increased along the successional gradient. Trends in phosphatase activity and Vmax correlated positively with plant biomass and negatively with concentrations of soluble reactive phosphorus in porewater, sediment extractable phosphorus, and total phosphourus. The porewater N∶P atom ratio decreased along the succession gradient from 25.3 in an early stage, open water community to 13.0 in a community dominated by emergent vegetation. The data also show that the distribution of the forms of phosphorus changed with successional stage. The change in distribution and the increased biological demand for phosphorus that paralleled succession were mediated by the activity of phosphatase enzymes.  相似文献   

9.
In order to avoid the pollution of trace metals in marine environment, it is necessary to establish the data and understand the mechanisms influencing the distribution of trace metals in marine environment. The concentration of heavy metals (Fe, Mn, Cr, Cu, Ni, Pb, Zn, Co and Cd) were studied in sediments of Ennore shelf, to understand the metal contamination due to heavily industrialized area of Ennore, south-east coast of India. Concentration of metals shows significant variability and range from 1.7 to 3.7% for Fe, 284–460 μg g−1 for Mn, 148.6–243.2 μg g−1 for Cr, 385–657 μg g−1 for Cu, 19.8–53.4 μg g−1 for Ni, 5.8–11.8 μg g−1 for Co, 24.9–40 μg g−1 for Pb, 71.3–201 μg g−1 for Zn and 4.6–7.5 μg g−1 for Cd. For various metals the contamination factor (CF) and geoaccumulation index (I geo) has been calculated to assess the degree of pollution in sediments. The geoaccumulation index shows that Cd, Cr and Cu moderately to extremely pollute the sediments. This study shows that the major sources of metal contamination in the Ennore shelf are land-based anthropogenic ones, such as discharge of industrial wastewater, municipal sewage and run-off through the Ennore estuary. The intermetallic relationship revealed the identical behavior of metals during its transport in the marine environment.  相似文献   

10.
Three undisturbed sediment samples were collected from the intertidal zone of the Jiaojiang Estuary of Zhejiang Province, China. The sediments were found to contain remarkably low concentrations of organic carbon (<0.6%) and acid volatile sulfide (AVS) (<30 μmol g−1). The availability of these two substrates likely constrained sulfate reduction and pyritization of several trace metals, respectively. This was especially true at one station where AVS concentrations in the upper 20 cm averaged less than 0.05 μmol g−1. Although the depth dependence of the degree of trace metal pyritization was generally consistent with expectations based on redox conditions, depth profiles of reactive-metal and pyrite-metal concentrations in several cases revealed more complex behavior and a positive correlation between reactive-metal concentrations and pore water metal concentrations.  相似文献   

11.
RTK-GPS data, aerial photographs and Aster images were used to quantify volume, surface elevation, terminus position and area changes of Glacier No. 4 of Sigong River over Mt. Bogda, Tianshan during the period from 1962 to 2009. Glacier surface elevation of the tongue area decreased by 15 ± 8 m (0.32 ± 0.17 m a−1) and ice volume loss reached 0.014 ± 0.008 km3 (0.013 ± 0.007 km3 w. e.). The glacier terminus retreated at a rate of 8.0 m a−1 and the area decreased by about 0.53 km2, accounting for 15.8% of the glacier area in 1962 (3.33 km2). The changes can be primarily attributed to the significant increase in temperature in this region. A comparison with glacier changes by field measurements in other regions of eastern Tianshan showed obvious spatial differences in the magnitude of the changes, owing to a combination of regional climate change and topographical factors.  相似文献   

12.
Diffusion of tetravalent cations in zircon   总被引：18，自引：1，他引：18  
Diffusion rates for the three tetravalent cations U, Th and Hf have been measured in synthetic zircon. Diffusant sources included oxide powders and ground pre-synthesized silicates. Rutherford backscattering spectrometry (RBS) was used to measure depth profiles. Over the temperature range 1400–1650 °C, the following Arrhenius relations were obtained (diffusion coefficients in m2sec−1): log D Th = (1.936 ± 0.9820) + (− 792 ± 34 kJ mol−1 /2.303 RT) log D U = (0.212 ± 2.440) + (− 726 ± 83 kJ mol−1 /2.303 RT) log D Hf = (3.206 ± 1.592) + (− 812 ± 54 kJ mol−1 /2.303 RT) The data show a systematic increase in diffusivity with decreasing ionic radius (i.e., faster diffusion rates for Hf than for U or Th), a trend also observed in our earlier study of rare earth diffusion in zircon. Diffusive fractionation may be a factor in the Lu-Hf system given the much slower diffusion rates of tetravalent cations when compared with the trivalent rare earths. The very slow diffusion rates measured for these tetravalent cations suggest that they are essentially immobile under most geologic conditions, permitting the preservation of fine-scale chemical zoning and isotopic signatures of inherited cores. Received: 12 July 1996 / Accepted: 2 December 1996  相似文献   

13.
A 52-yr record of dissolved oxygen in Chesapeake Bay (1950–2001) and a record of nitrate (NO3 −) loading by the Susquehanna River spanning a longer period (1903, 1945–2001) were assembled to describe the long-term pattern of hypoxia and anoxia in Chesapeake Bay and its relationship to NO3 − loading. The effect of freshwater inflow on NO3 − loading and hypoxia was also examined to characterize its effect at internannual and longer time scales. Year to year variability in river flow accounted for some of the observed changes in hypoxic volume, but the long-term increase was not due to increased river flow. From 1950–2001, the volume of hypoxic water in mid summer increased substantially and at an accelerating rate. Predicted anoxic volume (DO<0.2 mg I−1) at average river flow increased from zero in 1950 to 3.6×109 m3 in 2001. Severe hypoxia (DO<1.0 mg I−1) increased from 1.6×109 to 6.5×109 m3 over the same period, while mild hypoxia (DO<2.0 mg I−1) increased from 3.4×109 to 9.2×109 m3. NO3 − concentrations in the Susquehanna River at Harrisburg, Pennsylvania, increased up to 3-fold from 1945 to a 1989 maximum and declined through 2001. On a decadal average basis, the superposition of changes in river flow on the long-term increase in NO3 − resulted in a 2-fold increase in NO3 − loading from the Susquehanna River during the 1960s to 1970s. Decadal average loads were subsequently stable through the 1990s. Hypoxia was positively correlated with NO3 − loading, but more extensive hypoxia was observed in recent years than would be expected from the observed relationship. The results suggested that the Bay may have become more susceptible to NO3 − loading. To eliminate or greatly reduce anoxia will require reducing average annual total nitrogen loading to the Maryland mainstem Bay to 50×106 kg yr−1, a reduction of 40% from recent levels.  相似文献   

14.
To determine the removal of regenerated nitrogen by estuarine sediments, we compared sediment N2 fluxes to the stoichiometry of nutrient and O2 fluxes in cores collected in the Childs River, Cape Cod, Massachusetts. The difference between the annual PO4 3− (0.2 mol P m−2 yr−1) and NH4 + (1.6 mol N m−2 yr−1) flux and the Redfield N∶P ratio of 16 suggested an annual deficit of 1.5 mol N m−2 yr−1. Denitrification predicted from O2∶NH4 + flux ratios and measured as N2 flux suggested a nitrogen sink of roughly the same magnitude (1.4 mol N m−2 yr−1). Denitrification accounted for low N∶P ratios of benthic flux and removed 32–37% of nitrogen inputs entering the relatively highly nutrient loaded Childs River, despite a relatively brief residence time for freshwater in this system. Uptake of bottom water nitrate could only supply a fraction of the observed N2 flux. Removal of regenerated nitrogen by denitrification in this system appears to vary seasonally. Denitrification efficiency was inversely correlated with oxygen and ammonium flux and was lowest in summer. We investigated the effect of organic matter on denitrification by simulating phytoplankton deposition to cores incubated in the lab and by deploying chambers on bare and macroaglae covered sediments in the field. Organic matter addition to sediments increased N2 flux and did not alter denitrification efficiency. Increased N2 flux co-varied with O2 and NH4 + fluxes. N2 flux (261±60 μmol m−2 h−1) was lower in chambers deployed on macroalgal beds than deployed on bare sediments (458±70 μmol m−2 h−1), and O2 uptake rate was higher in chambers deployed on macroalgal beds (14.6±2.2 mmol m−2 h−1) than on bare sediments (9.6±1.5 mmol m−2 h−1). Macroalgal cover, which can retain nitrogen in the system, is a link between nutrient loading and denitrification. Decreased denitrification due to increasing macroalgal cover could create a positive feedback because decreasing denitrification would increase nitrogen availability and could increase macroalgae cover.  相似文献   

15.
Concentrations of polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) were measured in 13 surficial sediment samples collected at three lacustrine locations in the surroundings of Mexico City and four coastal areas of the States of Sinaloa, Sonora, Oaxaca and Veracruz. Total PCB concentrations span the interval 3.18–621 ng g−1. The highest values (63.7–621 ng g−1) were found in Mexico City, which is a highly anthropogenically impacted area, whereas low concentrations (3.18–12.9 ng g−1) were characteristic of seven places, some of them subject to intense hydrodynamics. In these latter cases, values increase by 18–73 times if normalised against the fine fraction (silt plus clay) content in sediment. Two samples from Mexico City exceed the ERM (Effect Range Median) guidelines and are likely to cause adverse effects. Samples contain only lower chlorinated PCBs (mainly 2-, 3- and 4-CB), thus suggesting that the most used PCB commercial mixture was Aroclor 1242. The homologue composition of the sample taken close to the nuclear power plant of Laguna Verde is identical to this commercial mixture. PAHs in the same samples have relatively low concentrations (14.9–287 ng g−1), well below ERL (Effect Range Low) guidelines. The composition of PAH mixtures accounts for the influence of both petrogenic and pyrolitic sources, with these latter prevailing at some places in Mexico City.  相似文献   

16.
Daily and annual integrated rates of primary productivity and community respiration were calculated using physiological parameters measured in oxygen-based photosynthesis-irradiance (P-I) incubations at 8 stations throughout central and western Long Island Sound (cwLIS) during the summer and autumn of 2002 and 2003 and the late spring of 2003. Each calculation takes into account actual variations in incident irradiance over the day and underwater irradiance and standing stock with depth. Annual peak rates, ±95% confidence interval of propagated uncertainty in each measurement, of gross primary production (GPP, 1,730±610 mmol O2 m−2 d−1), community respiration (Rc, 1,660±270 mmol O2 m−2 d−1), and net community production (NCP, 1,160±1,100 mmol O2 m−2 d−1) occurred during summer at the western end of the Sound. Lowest rates of GPP (4±11 mmol O2 m−2 d−1), Rc (−50±300 mmol O2 m−2 d−1), and NCP (−1,250±270 mmol O2 m−2 d−1) occurred during late autumn-early winter at the outer sampled stations. These large ranges in rates of GPP, Rc, and NCP throughout the photic zone of cwLIS are attributed to seasonal and spatial variability. Algal respiration (Ra) was estimated to consume an average of 5% to 52% of GPP, using a literature-based ratio of Ra:Rc. From this range, we established that the estimated Ra accounts for approximately half of GPP, and was used to estimate daily net primary production (NPP), which ranged from 2 to 870 mmol O2 m−2 d−1 throughout cwLIS during the study. Annual NPP averaged 40±8 mol O2 m−2 yr−1 for all sampled stations, which more than doubled along the main axis of the Sound, from 32±14 mol O2 m−2 yr−1 at an eastern station to 82±25 mol O2 m−2 yr−1 at the western-most station. These spatial gradients in productivity parallel nitrogen loads along the main axis of the Sound. Daily integrals of productivity were used to test and formulate a simple, robust biomass-light model for the prediction of phytoplankton production in Long Island Sound, and the slope of the relationship was consistent with reports for other systems.  相似文献   

17.
Responses of autotrophic and heterotrophic processes to nutrients and trace elements were examined in a series of experimental estuarine food webs of increasing trophic complexity using twenty 1-m3 mesocosms. Nutrients (nitrogen and phosphorus) and trace elements (a mix of arsenic, copper, cadmium) were added alone and in combination during four experimental runs spanning from spring 1997 to spring 1998. Diel changes in dissolved oxygen were used to examine whole system gross primary production (WS-GPP), respiration (WS-RESP), and net ecosystem metabolism (NEM). Nutrient and trace element additions had the greatest effect on WS-GPP, WS-RESP, and NEM; trophic complexity did not significantly affect any of these parameters (p>0.3). Effects of trophic complexity were detected in nutrient tanks where bivalves significantly (p=0.03) reduced WS-GPP. Nutrient additions significantly enhanced WS-GPP and to a lesser extent WS-RESP during most mesocosm runs. The system shifted from net heterotrophy (−17.2±1.8 mmol C m−3 d−1) in the controls to net autotrophy (29.1±7.6 mmol C m−3 d−1) in the nutrient tanks. The addition of trace elements alone did not affect WS-GPP and WS-RESP to the same extent as nutrients, and their effects were more variable. Additions of trace elements alone consistently made the system more net heterotrophic (−24.9±1.4 mmol C m−3 d−1) than the controls. When trace elements were added in combination with nutrients, the nutrient-enriched system became less autotrophic (1.6±3.1 mmol C m−3 d−1). The effects of trace elements on NEM occurred primarily through reductions in WS-GPP rather than increases in WS-RESP. Our results suggest that autotrophic and heterotrophic processes respond differently to these stressors.  相似文献   

18.
A black shale sample collected from the Chimiari site(Tarbela) was analyzed for elemental contents.Inductively coupled plasma-optical emission spectrometry(ICP-OES) was employed to determine major and trace elements in the digests.Precise analysis was accomplished for the black shales,which was better than 2.0%.Result shows that the shales are very rich in Ca(25439 μg·g-1),Fe(13933 μg·g-1),Ti(6932 μg·g-1),Al(5993 μg·g-1) and K(2730 μg·g-1).  相似文献   

19.
The heat capacity of gadolinium orthophosphate (GdPO4) measured in the temperature range 11.15–344.11 K by adiabatic calorimetry and available literature data were used to calculate its thermodynamic functions at 0–1600 K. At 298.15 K, these functions are as follows: C p 0(298.15 K) = 101.85 ± 0.05 J K−1 mol−1, S 0(298.15 K) = 123.82 ± 0.18 J K−1 mol−1, H 0(298.15 K)–H 0(0) = 17.250 ± 0.012 kJ mol−1, and Φ 0(298.15 K) = 65.97 ± 0.18 J K−1 mol−1 The calculated Gibbs free energy of formation from the elements of GdPO4 is Δ f G 0 (298.15 K) = −1844.3 ± 4.7 kJ mol−1.  相似文献   

20.
We measured seasonal variations in microzooplankton grazing in Long Island Sound (LIS) and San Francisco Bay (SFB). There was consistent evidence of nutrient limitation in LIS, but not SFB. We found higher chlorophyll a concentrations in LIS compared with SFB. In spite of differences in phytoplankton, there were no differences in microzooplankton abundance (summer: LIS, 12.4 ± 1.8 × 103 indiv. L−1; SFB, 14.1 ± 3.0 × 103 indiv. L−1), biomass (summer: LIS, 30.4 ± 5.0 μg C L−1; SFB, 26.3 ± 5.9 μg C L−1), or grazing rates (summer: LIS, 0.66 ± 0.19 day−1; SFB, 0.65 ± 0.18 day−1) between the two estuaries. In common with many other investigators, we found many instances of saturated as well as insignificant grazing. We suggest that saturation in some cases may result from high particle loads in turbid estuarine systems and that insignificant grazing may result from extreme saturation of the grazing response due to the need to process non-food particles.  相似文献   

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