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1.
Estimating the amount of gas-hydrate and free-gas is difficult in deep seas even with scientific coring and downhole measurements. Well data may be incompatible between holes of a site as well as with depth in the same hole. In this paper, we demonstrate an approach to estimate saturation of gas-hydrate from seismic velocities at any site where data set is limited. The study is carried out in the outer Blake Ridge, which is one of the most intensively studied regions of natural gas-hydrate occurrences and a very distinctive example of studying geophysical signatures of gas-hydrate and free-gas in deep marine sediments. Although, downhole measurements from both vertical seismic profiles (VSPs) and sonic logs provide the most accurate and direct measurements of velocity, only VSP velocities at Ocean Drilling Program (ODP) Sites 994, 995, and 997 on the Blake Ridge are used to estimate the saturation of gas-hydrate and free-gas as sonic logs at ODP sites are not reliable. Here we derive a general trend of the background velocity with depth using the porosity and mineralogy from coring at discrete depth intervals. Saturations of gas-hydrate and free-gas are then estimated from this background velocity using the effective medium modeling. The porosity and mineralogical compositions are taken from four different depths at Site 995, as data quality is the best in this hole. Average saturations of gas-hydrate and free-gas at three holes are estimated as 10–14 and 2–3%, respectively.  相似文献   

2.
The most commonly used marker for the investigation of gas-hydrates is the bottom simulating reflector (BSR), which is caused by gas-hydrate laden sediment underlain by either brine or gas-saturated sediment. A BSR has been identified by seismic experiment in the Kerala-Konkan Basin of the western continental margin of India. Here we perform AVA modeling of seismic reflection data from a BSR to investigate the seismic velocities for quantitative assessment of gas-hydrates and to understand the origin of the BSR. The result reveals a P-wave velocity of 2.245 km/s and an S-wave velocity of 0.895 km/s for the sediments above the BSR. This corresponds to a Poisson ratio of 0.406 and hydrates saturation of ∼30% in the study area. The comparison of estimated P-wave velocity (1.77 km/s) above the hydrates-bearing sediment to that (1.78 km/s) below the BSR implies that the origin of the BSR is mainly due to gas-hydrates, as the presence (even in small quantities) of free-gas reduces the P-wave velocity considerably.  相似文献   

3.
Gas hydrate stability conditions restrict the occurrence of gas hydrate to unconsolidated and high water-content sediments at shallow depths. Because of these host sediments properties, seismic and well log data acquired for the detection of free gas and associated gas hydrate-bearing sediments often require nonconventional analysis. For example, a conventional method of identifying free gas using the compressional/shear-wave velocity (Vp/Vs) ratio at the logging frequency will not work, unless the free-gas saturations are more than about 40%. The P-wave velocity dispersion of partially gas-saturated sediments causes a problem in interpreting well log velocities and seismic data. Using the White, J.E. [1975. Computed seismic speeds and attenuation in rocks with partial gas saturation. Geophysics 40, 224–232] model for partially gas-saturated sediments, the difference between well log and seismic velocities can be reconciled. The inclusion of P-wave velocity dispersion in interpreting well log data is, therefore, essential to identify free gas and to tie surface seismic data to synthetic seismograms.  相似文献   

4.
Coastal upwelling systems are regions with highly variable physical processes and very high rates of primary production and very little is known about the effect of these factors on the short-term variations of CO2 fugacity in seawater (fCO2w). This paper presents the effect of short-term variability (<1 week) of upwelling–downwelling events on CO2 fugacity in seawater (fCO2w), oxygen, temperature and salinity fields in the Ría de Vigo (a coastal upwelling ecosystem). The magnitude of fCO2w values is physically and biologically modulated and ranges from 285 μatm in July to 615 μatm in October. There is a sharp gradient in fCO2w between the inner and the outer zone of the Ría during almost all the sampling dates, with a landward increase in fCO2w.CO2 fluxes calculated from local wind speed and air–sea fCO2 differences indicate that the inner zone is a sink for atmospheric CO2 in December only (−0.30 mmol m−2 day−1). The middle zone absorbs CO2 in December and July (−0.05 and −0.27 mmol·m−2 day−1, respectively). The oceanic zone only emits CO2 in October (0.36 mmol·m−2 day−1) and absorbs at the highest rate in December (−1.53 mmol·m−2 day−1).  相似文献   

5.
Biochemical characterization of cholinesterase activity (ChE) was carried out on the Antarctic scallop Adamussium colbecki collected in winter 2000 from Campo Icaro (Ross Sea, Antarctica) in order to increase its suitability as a sentinel organism for monitoring the Antarctic environment. The digestive gland, gills and adductor muscle were investigated for substrate specificity and inhibitors sensitivity using acetylthiocholine iodide (ASCh) and butyrylthiocholine iodide (BSCh) as substrates and tetra (monoisopropyl)pyrophosphor-tetramide (Iso-OMPA), 1,5-bis(4-allyldimethylammoniumphenyl)-penthan-3-one dibromide (BW284c51) and the insecticide chlorpyrifos as inhibitors. Effect of in vivo exposure to ZnCl2 was also investigated. All the tissues expressed ChE activity (gill > adductor muscle > digestive gland) and low substrates specificity throughout the hydrolysis of both ASCh and BSCh substrates. Partial (25–29%) and total inhibition (100%) of ChE activity in gills was demonstrated following in vitro incubation with Iso-OMPA and BW284c51 (3 mM), respectively. Concentration-dependent inhibition was also evident with chlorpyrifos in the range 10−4–10−10 M (IC50 10−6) while in vivo exposure to ZnCl2 did not seem to affect ChE activity in the scallop. The potential use of ChE in the A. colbecki as biomarker for monitoring water contamination in the marine Antarctic environment is discussed.  相似文献   

6.
The conditional acid dissociation constants (pKa′) of two sulfonephthalein dyes, thymol blue (TB) and m-cresol purple (mCP), were assessed throughout the estuarine salinity range (0<S<40) using a tris/tris–HCl buffer and spectrophotometric measurement. The salinity dependence of the pKa′ of both dyes was fitted to the equations (25 °C, total proton pH scale, mol kg soln−1):
The estimated accuracy of pH measurements using these calculated pKa′ values is considered to be comparable to that possible with careful use of a glass electrode (±0.01 pH unit) but spectrophotometric measurements in an estuary have the significant advantage that it is not necessary to calibrate an electrode at different salinities. pH was measured in an estuary over a tidal cycle with a precision of ±0.0005 pH unit at high (S>30) salinity, and ±0.002 pH unit at low (S<5) salinity. The pH increased rapidly in the lower salinity ranges (0<S<15) but less rapidly at higher salinities.  相似文献   

7.
Woei-Lih Jeng   《Marine Chemistry》2006,102(3-4):242-251
The n-alkane average chain length (ACL) is the weight-averaged number of carbon atoms of the higher plant C25–C33 n-alkanes. The abundance of individual n-alkanes from higher plant sources generally increases with increasing carbon number in coastal marine sediments around Taiwan, but this trend is reversed for petrogenic hydrocarbons. The ACL would potentially be lowered if petrogenic hydrocarbons were added to sediments containing biogenic hydrocarbons alone. To test this idea, a marine environment off southwestern Taiwan known to contain both biogenic and petrogenic hydrocarbons and two nearby rivers were selected for investigating possible difference in ACL values between their sediments. The average CPI of C25–C33 n-alkanes was 4.08 ± 2.04 (range 1.90–8.96, n = 15) for the river sediments and 1.70 ± 0.16 (range 1.43–1.97, n = 15) for the marine sediments. The ACL of C25–C33 n-alkanes for river sediments ranged from 29.2 to 30.5 (average 29.9 ± 0.4), and for marine sediments from 28.4 to 29.3 (average 28.9 ± 0.3). The ACL difference between marine and river sediments was significant (Student's t test at 99% confidence) although it appeared small. It is suggested that the ACL can be an additional indicator for detection of petrogenic hydrocarbons in coastal marine sediments.  相似文献   

8.
Monthly seawater pH and alkalinity measurements were collected between January 1996 and December 2000 at 10°30′N, 64°40′W as part of the CARIACO (CArbon Retention In A Colored Ocean) oceanographic time series. One key objective of CARIACO is to study temporal variability in Total CO2 (TCO2) concentrations and CO2 fugacity (fCO2) at this tropical coastal wind-driven upwelling site. Between 1996 and 2000, the difference between atmospheric and surface ocean CO2 concentrations ranged from about − 64.3 to + 62.3 μatm. Physical and biochemical factors, specifically upwelling, temperature, primary production, and TCO2 concentrations interacted to control temporal variations in fCO2. Air–sea CO2 fluxes were typically depressed (0 to + 10 mmol C m− 2 day− 1) in the first few months of the year during upwelling. Fluxes were higher during June–November (+ 10 to 20 mmol C m− 2 day− 1). Fluxes were generally independent of the slight changes in salinity normally seen at the station, but low positive flux values were seen in the second half of 1999 during a period of anomalously heavy rains and land-derived runoff. During the 5 years of monthly data examined, only two episodes of negative air–sea CO2 flux were observed. These occurred during short but intense upwelling events in March 1997 (−10 mmol C m− 2 day− 1) and March 1998 (− 50 mmol C m− 2 day− 1). Therefore, the Cariaco Basin generally acted as a source of CO2 to the atmosphere in spite of primary productivity in excess of between 300 and 600 g C m− 2 year− 1.  相似文献   

9.
A method of high resolution seismic velocity analysis for ocean bottom seismometer (OBS) records is applied to the study of the shallow oceanic crust, especially sedimentary and basement layers. This method is based on the direct-p mapping and the-sum inversion. We use data obtained from a 1989 airgun-OBS experiment in the northern Yamato Basin, Japan Sea and derive P- and S-wave velocity functions that can be compared with the seismic reflection profiles. Using split-spread profile records, we obtain interface dips and true interval velocities from the OBS data. These results show good agreement with the reflection profile records, the acoustic velocities of core samples, and sonic log profiles. We also present a method for estimating errors in the derived velocity functions by calculating covariance of the derived layers' thicknesses. The estimated depth errors are about 150 m at shallow depths, which is close to the seismic wavelength used. The high resolution of this method relies on accurate determination of shot positions by GPS, spatially dense seismic observations, and the use of unsaturated reflected waves arriving after the direct water wave that are observed on low-gain component records.  相似文献   

10.
The reproductive cycle of anchovy, Engraulis encrasicolus (L.), was studied from monthly random samples of purse seine catches. A total of 1477 anchovy specimens were collected from January to December 2003 in the Zrmanja River estuary (Novigrad Sea). The analysis was based on the temporal evolution of gonadosomatic index, mass and stage of gonads. The total length of anchovy ranged from 4.5 to 14.5 cm and mass from 0.56 to 19.80 g. Sex ratio was slightly different from 1:1; the females were insignificantly predominated (♂/♀ = 0.99). The period of reproductive activity was from April to September coinciding with the most developed stages of gonads as well as with the highest gonad weights, and gonadosomatic indices. To estimate the length at maturity, a sub sample of 454 anchovy was taken from May to July (peak of anchovy spawning period). The length at which 50% of anchovy were mature (L50) was calculated to be 8.2 cm. The length–weight relationship of anchovy was described by the expression: W = 3.51 × 10−3 LT3.211 (r2 = 0.998). The relationships between total length–standard length and total length–fork length are LT = 1.1405LS + 0.2420 and LT = 1.0425 LF + 0.3944, respectively.  相似文献   

11.
The seasonal and interannual variability of the air–sea CO2 flux (F) in the Atlantic sector of the Barents Sea have been investigated. Data for seawater fugacity of CO2 (fCO2sw) acquired during five cruises in the region were used to identify and validate an empirical procedure to compute fCO2sw from phosphate (PO4), seawater temperature (T), and salinity (S). This procedure was then applied to time series data of T, S, and PO4 collected in the Barents Sea Opening during the period 1990–1999, and the resulting fCO2sw estimates were combined with data for the atmospheric mole fraction of CO2, sea level pressure, and wind speed to evaluate F.The results show that the Atlantic sector of the Barents Sea is an annual sink of atmospheric CO2. The monthly mean uptake increases nearly monotonically from 0.101 mol C m− 2 in midwinter to 0.656 mol C m− 2 in midfall before it gradually decreases to the winter value. Interannual variability in the monthly mean flux was evaluated for the winter, summer, and fall seasons and was found to be ± 0.071 mol C m− 2 month− 1. The variability is controlled mainly through combined variation of fCO2sw and wind speed. The annual mean uptake of atmospheric CO2 in the region was estimated to 4.27 ± 0.68 mol C m− 2.  相似文献   

12.
We report several biogeochemical parameters (dissolved inorganic carbon (DIC), total alkalinity (TA), dissolved oxygen (DO), phosphate (PO4), nitrate + nitrite (NO3 + NO2), silicate (Si(OH)4)) in a region off Otaru coast in Hokkaido, Japan on a “weekly” basis during the period of April 2002–May 2003. To better understand the long-term temporal variations of the main factors affecting CO2 flux in this coastal region and its role as a sink/source of atmospheric CO2, we constructed an algorithm of DIC and TA using other hydrographic properties. We estimated the CO2 flux across the air–sea interface by using the classical bulk method. During 1998–2003 in our study region, the estimated fCO2sea ranged about 185–335 μatm. The maximum of fCO2sea in the summer was primarily due to the change of water temperature. The minimum of fCO2sea in the early spring can be explained not only by the change of water temperature but also the change of nutrients and chlorophyll-a. To clarify the factors affecting fCO2sea (water temperature, salinity, and biological activity), we carried out a sensitivity analysis of these effects on the variation of fCO2sea. In spring, the biological effect had the largest effect for the minimum of fCO2sea (40%). In summer, the water temperature effect had the largest effect for the maximum of fCO2sea (25%). In fall, the water temperature effect had the largest effect for the minimum of fCO2sea (53%). In winter, the biological effect had the largest effect for the minimum of fCO2sea (35%).We found that our study region was a sink region of CO2 throughout a year (−0.78 mol/m2/yr). Furthermore, we estimated that the increase of fCO2sea was about 0.56 μatm/yr under equilibrium with the atmospheric CO2 content for the period 1998–2003, with the temporal changes in the variables (T, S, PO4) on fCO2sea, thus as the maximum trend of each variable on fCO2sea was 0.22 μatm/yr, and the trend of residual fCO2 including gas exchange was 0.34 μatm/yr. This result suggests that interaction among variables would affect gas exchange between air and sea effects on fCO2sea. We conclude that this study region as a representative coastal region of marginal seas of the North Pacific is special because it was measured, but there is no particular significance in comparison to any other area.  相似文献   

13.
We analysed the alkenone unsaturation ratio (UK′37) in 87 surface sediment samples from the western South Atlantic (5°N–50°S) in order to evaluate its applicability as a paleotemperature tool for this part of the ocean. The measured UK′37 ratios were converted into temperature using the global core-top calibration of Müller et al. (1998) and compared with annual mean atlas sea-surface temperatures (SSTs) of overlying surface waters. The results reveal a close correspondence (<1.5°C) between atlas and alkenone temperatures for the Western Tropical Atlantic and the Brazil Current region north of 32°S, but deviating low alkenone temperatures by −2° to −6°C are found in the regions of the Brazil–Malvinas Confluence (35–39°S) and the Malvinas Current (41–48°S). From the oceanographic evidence these low UK′37 values cannot be explained by preferential alkenone production below the mixed layer or during the cold season. Higher nutrient availability and algal growth rates are also unlikely causes. Instead, our results imply that lateral displacement of suspended particles and sediments, caused by strong surface and bottom currents, benthic storms, and downslope processes is responsible for the deviating UK′37 temperatures. In this way, particles and sediments carrying a cold water UK′37 signal of coastal or southern origin are transported northward and offshore into areas with warmer surface waters. In the northern Argentine Basin the depth between displaced and unaffected sediments appears to coincide with the boundary between the northward flowing Lower Circumpolar Deep Water (LCDW) and the southward flowing North Atlantic Deep Water (NADW) at about 4000 m.  相似文献   

14.
This paper evaluates the simultaneous measurement of dissolved gases (CO2 and O2/Ar ratios) by membrane inlet mass spectrometry (MIMS) along the 180° meridian in the Southern Ocean. The calibration of pCO2 measurements by MIMS is reported for the first time using two independent methods of temperature correction. Multiple calibrations and method comparison exercises conducted in the Southern Ocean between New Zealand and the Ross Sea showed that the MIMS method provides pCO2 measurements that are consistent with those obtained by standard techniques (i.e. headspace equilibrator equipped with a Li–Cor NDIR analyser). The overall MIMS accuracy compared to Li–Cor measurements was 0.8 μatm. The O2/Ar ratio measurements were calibrated with air-equilibrated seawater standards stored at constant temperature (0 ± 1 °C). The reproducibility of the O2/Ar standards was better than 0.07% during the 9 days of transect between New Zealand and the Ross Sea.The high frequency, real-time measurements of dissolved gases with MIMS revealed significant small-scale heterogeneity in the distribution of pCO2 and biologically-induced O2 supersaturation (ΔO2/Ar). North of 65°S several prominent thermal fronts influenced CO2 concentrations, with biological factors also contributing to local variability. In contrast, the spatial variation of pCO2 in the Ross Sea gyre was almost entirely attributed to the biological utilization of CO2, with only small temperature effects. This high productivity region showed a strong inverse relationship between pCO2 and biologically-induced O2 disequilibria (r2 = 0.93). The daily sea air CO2 flux ranged from − 0.2 mmol/m2 in the Northern Sub-Antarctic Front to − 6.4 mmol/m2 on the Ross Sea shelves where the maximum CO2 influx reached values up to − 13.9 mmol/m2. This suggests that the Southern Ocean water (south of 58°S) acts as a seasonal sink for atmospheric CO2 at the time of our field study.  相似文献   

15.
The uptake of atmospheric carbon dioxide in the water transported over the Bering–Chukchi shelves has been assessed from the change in carbon-related chemical constituents. The calculated uptake of atmospheric CO2 from the time that the water enters the Bering Sea shelf until it reaches the northern Chukchi Sea shelf slope (1 year) was estimated to be 86±22 g C m−2 in the upper 100 m. Combining the average uptake per m3 with a volume flow of 0.83×106 m3 s−1 through the Bering Strait yields a flux of 22×1012 g C year−1. We have also estimated the relative contribution from cooling, biology, freshening, CaCO3 dissolution, and denitrification for the modification of the seawater pCO2 over the shelf. The latter three had negligible impact on pCO2 compared to biology and cooling. Biology was found to be almost twice as important as cooling for lowering the pCO2 in the water on the Bering–Chukchi shelves. Those results were compared with earlier surveys made in the Barents Sea, where the uptake of atmospheric CO2 was about half that estimated in the Bering–Chukchi Seas. Cooling and biology were of nearly equal significance in the Barents Sea in driving the flux of CO2 into the ocean. The differences between the two regions are discussed. The loss of inorganic carbon due to primary production was estimated from the change in phosphate concentration in the water column. A larger loss of nitrate relative to phosphate compared to the classical ΔN/ΔP ratio of 16 was found. This excess loss was about 30% of the initial nitrate concentration and could possibly be explained by denitrification in the sediment of the Bering and Chukchi Seas.  相似文献   

16.
On the Vøring volcanic passive margin offshore mid-Norway, NE Atlantic, a lower crustal body with P-wave velocities in the range of 7.1–7.7 km/s has been mapped by twenty two-dimensional Ocean Bottom Seismograph (OBS) profiles. The main aim of the present paper is to evaluate to what extent the lower crust is consistent with magmatic intrusions or serpentinized peridotite. The relatively low V p/V s ratios of 1.75–1.78 modelled for the lower crust under the continental part of the Vøring Plateau are consistent with mafic intrusions mixed with blocks of stretched continental crust, but not with the presence of partially serpentinized peridotites. The lower crustal high-velocity body is restricted to the area of the Late Cretaceous/Early Tertiary rift that lead to continental break-up in Early Eocene. The same model can explain the observations in the northern Vøring Basin, but in the central and southern Vøring Basin the seismic velocities do not preclude a model involving serpentinized peridotite in addition to intrusions and continental remnants. On the west Iberia non-volcanic margin a similar layer is interpreted as serpentinized peridotite. The existence of Moho reflections, the observation of S-wave anisotropy but absence of P-wave anisotropy, uncertainties regarding supply of water to allow for significant serpentinization and very low stretching factors compared with the west Iberia Margin, are among factors that argue against the presence of serpentinized peridotite in the Vøring Basin.  相似文献   

17.
Alkenone unsaturation indices (UK37 and UK′37) have long been used as proxies for surface water temperature in the open ocean. Recent studies have suggested that in other marine environments, variables other than temperature may affect both the production of alkenones and the values of the indices. Here, we present the results of a reconnaissance field study in which alkenones were extracted from particulate matter filtered from the water column in Chesapeake Bay during 2000 and 2001. A multivariate analysis shows a strong positive correlation between UK37 (and UK′37) values and temperature, and a significant negative correlation between UK37 (and UK′37) values and nitrate concentrations. However, temperature and nitrate concentrations also co-vary significantly. The temperature vs. UK37 relationships (UK37=0.018 (T)−0.162, R2=0.84, UK′37=0.013 (T)−0.04, R2=0.80) have lower slopes than the open-ocean equations of Prahl et al. [1988. Further evaluation of long-chain alkenones as indicators of paleoceanographic conditions. Geochimica et Cosmochimica Acta 52, 2303–2310] and Müller et al. [1998. Calibration of the alkenone paleotemperature index UK′37 based on core-tops from the eastern South Atlantic and the global ocean (60°N–60°S). Geochimica et Cosmochimica Acta 62, 1757–1772], but are similar to the relationships found in controlled studies with elevated nutrient levels and higher nitrate:phosphate (N:P) ratios. This implies that high nutrient levels in Chesapeake Bay have either lowered the UK37 vs. temperature slope, or nutrient levels are the main controller of the UK37 index. In addition, particularly high abundances (>5% of total C37 alkenones) of the tetra-unsaturated ketone, C37:4, were found when water temperatures reached 25 °C or higher, thus posing further questions about the controls on alkenone production as well as the biochemical roles of alkenones.  相似文献   

18.
We describe the fabrication of organically modified sol–gel (ORMOSIL) planar optodes for mapping the two-dimensional oxygen distribution in sediments. All sensor foils were based on the use of ruthenium(II)-tris-(4,7-diphenyl-1,10-phenantrolin)-perchlorate, which is a fluorescent dye quenched dynamically by oxygen. Sensors made with different sol–gel immobilisation matrices, different concentrations of precursors and indicator dye, as well as different types of scattering particles co-immobilised in the sensor foil were investigated systematically. Optimal sensor performance was obtained with dye concentrations of 2–10 mmol/kg in an immobilisation matrix made of diphenyldiethoxy-silan and phenyltriethoxy-silan precursors with addition of organically coated TiO2 particles. The sensors exhibited a good mechanical stability and a high sensitivity from 0% to 100% oxygen, which remained constant over at least 36 days. The planar optodes were used with a fluorescent lifetime imaging system for direct mapping of the spatio-temporal variation in oxygen distribution within marine sediment inhabited by the polychaete Hediste diversicolor. The measurements demonstrated the spatio-temporal heterogeneity of the oxygen distribution in bioturbated sediments due to burrow structures and non-constant irrigation activity of the polychaete, which is difficult to resolve with microsensors or with traditional biogeochemical techniques.  相似文献   

19.
An improved model is presented for the calculation of the solubility of carbon dioxide in aqueous solutions containing Na+, K+, Ca2+, Mg2+, Cl−, and SO42− in a wide temperature–pressure–ionic strength range (from 273 to 533 K, from 0 to 2000 bar, and from 0 to 4.5 molality of salts) with experimental accuracy. The improvements over the previous model [Duan, Z. and Sun, R., 2003. An improved model calculating CO2 solubility in pure water and aqueous NaCl solutions from 273 to 533K and from 0 to 2000 bar. Chemical Geology, 193: 257–271] include: (1) By developing a non-iterative equation to replace the original equation of state in the calculation of CO2 fugacity coefficients, the new model is at least twenty times computationally faster and can be easily adapted to numerical reaction-flow simulator for such applications as CO2 sequestration and (2) By fitting to the new solubility data, the new model improved the accuracy below 288 K from 6% to about 3% of uncertainty but still retains the high accuracy of the original model above 288 K. We comprehensively evaluate all experimental CO2 solubility data. Compared with these data, this model not only reproduces all the reliable data used for the parameterization but also predicts the data that were not used in the parameterization. In order to facilitate the application to CO2 sequestration, we also predicted CO2 solubility in seawater at two-phase coexistence (vapor–liquid or liquid–liquid) and at three-phase coexistence (CO2 hydrate–liquid water–vapor CO2 [or liquid CO2]). The improved model is programmed and can be downloaded from the website http://www.geochem-model.org/programs.htm.  相似文献   

20.
Elemental (TOC, TN, C/N) and stable carbon isotopic (δ13C) compositions and n-alkane (nC16–38) concentrations were measured for Spartina alterniflora, a C4 marsh grass, Typha latifolia, a C3 marsh grass, and three sediment cores collected from middle and upper estuarine sites from the Plum Island salt marshes. Our results indicated that the organic matter preserved in the sediments was highly affected by the marsh plants that dominated the sampling sites. δ13C values of organic matter preserved in the upper fresh water site sediment were more negative (−23.0±0.3‰) as affected by the C3 plants than the values of organic matter preserved in the sediments of middle (−18.9±0.8‰) and mud flat sites (−19.4±0.1‰) as influenced mainly by the C4 marsh plants. The distribution of n-alkanes measured in all sediments showed similar patterns as those determined in the marsh grasses S. alterniflora and T. latifolia, and nC21 to nC33 long-chain n-alkanes were the major compounds determined in all sediment samples. The strong odd-to-even carbon numbered n-alkane predominance was found in all three sediments and nC29 was the most abundant homologue in all samples measured. Both δ13C compositions of organic matter and n-alkane distributions in these sediments indicate that the marsh plants could contribute significant amount of organic matter preserved in Plum Island salt marsh sediments. This suggests that salt marshes play an important role in the cycling of nutrients and organic carbon in the estuary and adjacent coastal waters.  相似文献   

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