首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 78 毫秒
1.
Intense thermochemical sulfate reduction (TSR) and up to 18% H2S are found in the Upper Permian Changxing Formation (P3ch) in the northeast (NE) Sichuan Basin, China, despite that rare gypsum or anhydrite was found in this formation. Here, we present new concentration data of carbonate-associated sulfate (CAS) from carbonate host rocks, C, O, and Sr isotope data for TSR-related calcites, and S isotope data for sulfur compounds obtained during this study. These data along with spatial-temporal changes in palaeogeopressure conditions, hydraulic conductivity and the physical capacity indicate that the H2S was generated locally from TSR within the P3ch reservoirs. We propose that the reactive sulfates were derived from CAS released during dolomitization and recrystallization of earlier dolomite within the P3ch Fm. and from the cross-formational migration of evaporative brines from the Lower Triassic Feixianguan Formation (T1f) to P3ch Fm. Our calculation shows that the two sources could provide enough SO42− for the generation of H2S within the P3ch reservoirs. Early downward migration of sulfate-rich evaporative brines from the T1f formation occurred in near-surface and shallow burial diagenetic settings (mainly <1000 m). The evaporative brines seeped into porous grainstones and displaced preexisting seawater, causing pervasive dolomitization within the P3ch Fm. Subsequently, TSR calcites precipitated from the pore water have high Sr concentrations (up to 7767 ppm), close to the T1f TSR calcites, and 87Sr/86Sr ratios mainly from 0.7074 to 0.7078, which are significantly higher than those of Late Permian seawater but within the range of early Triassic seawater.  相似文献   

2.
The speciation of sedimentary sulfur (pyrite, acid volatile sulfides (AVS), S0, H2S, and sulfate) was analyzed in surface sediments recovered at different water depths from the northwestern margin of the Black Sea. Additionally, dissolved and dithionite-extractable iron were quantified, and the sulfur isotope ratios in pyrite were measured. Sulfur and iron cycling in surface sediments of the northwestern part of the Black Sea is largely influenced by (1) organic matter supply to the sediment, (2) availability of reactive iron compounds and (3) oxygen concentrations in the bottom waters. Biologically active, accumulating sediments just in front of the river deltas were characterized by high AVS contents and a fast depletion of sulfate concentration with depth, most likely due to high sulfate reduction rates (SRR). The δ34S values of pyrite in these sediments were relatively heavy (−8‰ to −21‰ vs. V-CDT). On the central shelf, where benthic mineralization rates are lower, re-oxidation processes may become more important and result in pyrite extremely depleted in δ34S (−39‰ to −46‰ vs. V-CDT). A high variability in δ34S values of pyrite in sediments from the shelf-edge (−6‰ to −46‰ vs. V-CDT) reflects characteristic fluctuations in the oxygen concentrations of bottom waters or varying sediment accumulation rates. During periods of oxic conditions or low sediment accumulation rates, re-oxidation processes became important resulting in low AVS concentrations and light δ34S values. Anoxic conditions in the bottom waters overlying shelf-edge sediments or periods of high accumulation rates are reflected in enhanced AVS contents and heavier sulfur isotope values. The sulfur and iron contents and the light and uniform pyrite isotopic composition (−37‰ to −39‰ vs. V-CDT) of sediments in the permanently anoxic deep sea (1494 m water depth) reflect the formation of pyrite in the upper part of the sulfidic water column and the anoxic surface sediment. The present study demonstrates that pyrite, which is extremely depleted in 34S, can be found in the Black Sea surface sediments that are positioned both above and below the chemocline, despite differences in biogeochemical and microbial controlling factors.  相似文献   

3.
The reaction pathways of nitrogen and carbon in the Framvaren Fjord (Norway) were studied through stable isotope analysis (δ15N and δ13C) of dissolved inorganic and particulate organic matter (POM). The variations in the isotopic compositions of the various C and N pools within the water column were use to evaluate the historical deposition of material to the sediments. The high δ15N-NH4+ at the O2/H2S interface, as a consequence of microbial uptake between 19 and 25 m, results in extremely depleted δ15N-particulate nitrogen (PN) of approximately 1‰ within the particulate maximum at approximately 19 m. The carbon isotopic distribution of dissolved inorganic carbon (DIC) and particulate organic carbon (POC) within the interface suggests that the distinct microbial flora (Chromatium sp. and Chlorobium sp.) fractionate inorganic carbon to different degrees. The extremely light δ13C-POC within the interface (−31‰) appears to be a result of carbon uptake by Chromatium sp. while δ13C-POC of −12‰ is more indicative of Chlorobium sp. Nitrogen isotopic mass balance calculations suggested that approximately 75% of the material sinking to the sediments was derived from the dense particulate maximum between 19 and 25 m. The sediment distribution of nitrogen isotopes varied from 2‰ at the surface to approximately 6‰ at 30 cm. The nitrogen isotopic variations with depth may be an indicator of the depth or position of the O2/H2S interface in the fjord. Low sediment δ15N indicated that the interface was within the photic zone of the water column, while more enriched values suggested that the interface was lower in the water column potentially allowing for less fractionation during biological incorporation of dissolved inorganic nitrogen. Results indicate that the dense layers of photo-autotrophic bacteria in the upper water column impart unique carbon and nitrogen isotopic signals that help follow processes within the water column and deposition to the sediments.  相似文献   

4.
The ion product of water in seawater and the total activity coefficients of hydroxide and hydrogen ions were determined over the temperature range 2° to 35°C, and the salinity range 20‰ to 44‰. At 25°C and 35‰ salinity, the measured values are pKWSW = 13.20, fOH = 0.22, fH = 0.71 on the molar concentration scale.  相似文献   

5.
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   

6.
The Yuanba gas field in the Permian Changxing Formation (P2c), which exhibits wide variations in its hydrogen sulfide (H2S) concentration (1.20–12.16%), is a typical sour gas field in the northern Sichuan Basin. The sulfur-rich reservoir's solid bitumen (atomic S/C ratios are 0.032–0.142), and late calcite cement δ13C values, which are smaller than the δ13C values of the host dolostone, indicate that the H2S originated from thermal sulfate reduction (TSR) and oil was involved in TSR. The gas souring index (GSI) of P2c's gases is generally lower than 0.1. The ethane δ13C values increase as the GSI increases, although no obvious increase was observed in the methane δ13C values. The calcite cements' δ13C values (−15.36 to +4.56‰) in dolostone are heavier than the typical reported values, which implies that only limited heavy hydrocarbon gases were involved in TSR. No anhydrites developed in P2c's reservoirs, and dissolved sulfate anions (SO42−) were mainly enriched during dolomitization. Insufficient dissolved SO42− most likely caused the lower H2S concentrations in the Permian to Triassic reservoirs in the northeastern Sichuan Basin compared to the Permian Khuff Formation in Saudi Arabia and the Jurassic Smackover Formation in Mississippi. Except for the SO42− in residual water in paleo-oil zones, SO42− from bottom water may also be involved in TSR; therefore, oil reservoirs with bottom water have more SO42− and can produce more H2S than pure oil reservoirs. This phenomenon may be the main cause of the great difference in the H2S concentrations between reservoirs, while gravitational differentiation during late uplift most likely creates differences in H2S concentrations in a single reservoir. Carbon dioxide (CO2), which has a relatively heavy δ13C value (−3.9 to −0.3‰), may be the combined result of TSR, the balance between CO2 and inorganic fluid systems, and carbonate decomposition.  相似文献   

7.
Data from piston cores collected from Carolina Rise and Blake Ridge, and from many DSDP/ODP sites indicate that extreme 13C-depletion of methane and ΣCO2 occurs within the uppermost methanogenic zone of continental rise sediments. We infer that 13C-depleted methane is generated near the top of the methanogenic zone when carbon of 13C-depleted ΣCO2, produced by microbially-mediated anaerobic methane oxidation, is recycled back to methane through CO2 reduction. Interstitial water and gas samples were collected in 27 piston cores, 16 of which penetrated through the sulfate reduction zone into methane-bearing sediments of the Carolina Rise and Blake Ridge. Isotopic measurements (δ13CCH4, δ13CCO2, δDCH4, and δDH2O) indicate that this methane is microbial in origin, produced by microbially-mediated CO2 reduction. Methane samples form two distinct isotopic pools. (1) Methane from a seafloor seep site shows a mean δ13CCH4 value of − 69 ± 2%., mirroring values found at ≥ 160 mbsf from a nearby DSDP site. (2) Twenty, areally-separated sites (sample depth, 10 to 25 mbsf) have δ13CCH4 values ranging from −85 to −103%., and δ13CCO2 as negative as −48%.. The very low δ13C values from the methane and CO2 pools highlight the importance of carbon cycling within continental rise sediments at and near the sulfate-methane boundary.  相似文献   

8.
The apparent solubility product K′sp of calcite in seawater was measured as a function of temperature, salinity, and pressure using potentiometric saturometry techniques. The temperature effect was hardly discernible experimentally. The value of K′sp at 25°C was 4.59·10−7 mole2/(kg seawater)2 at 35‰S, 5.34·10−7 at 43‰S, and 3.24·10−7 at 27‰S. The apparent partial molal volume was found to be −34.4 cm3 at 25°C and −42.3 cm3 at 2°C from a linear fit of log(K′sp P/K′sp 1). These results were used in conjunction with field data to calculate the degree of saturation in the oceans and showed undersaturation at shallower depths than previously reported.  相似文献   

9.
The concentrations of total carbonate (Ct), sulphate, sulphide, thiols and oxygen, the ratio between the stable sulphur isotopes 34S and 32S in sulphate and sulphide, and the density (used to calculate salinity) were determined on samples from the water column of Framvaren, a superanoxic fjord in southern Norway. From a depth of 18m (the oxic-anoxic boundary) the initial sulphate concentration, ([SO4]init), as calculated from salinity, is significantly higher than the sum of the measured sulphur species. This is attributed to a loss of sulphur from the water column. The amount of total carbonate produced, corrected for the initial concentration (Ct - 2.4 Sal/35) is found to be proportional to the amount of sulphate consumed, ([SO4]init - [SO4]), according to the following relation Ct- 2.4 Sal/35 = 1.84 ([SO4]init - [SO4]). Isotopic fractionation caused by bacterial sulphate reduction in the anoxic part of the water column produces sulphide with a δ34S 40‰ lower than the δ34S for sulphate at corresponding depths. The isotopic fractionation also results in δ34S value for the remaining sulphate at depths below 80 m being considerably higher than the mean value for ocean water, which is close to + 20‰. The δ34S values for sulphate at depths between 10 and 50 m were lower than + 20‰ which indicates oxidation of sulphide, which follows upon diffusion of sulphide from deeper parts of the water column and inflow of oxygenated seawater over the sill into the anoxic water of the fjord. A conclusive scenario of the Framvaren sulphur chemistry is presented.  相似文献   

10.
The hydrolysis of silicic acid, Si(OH)4, was studied in a simplified seawater medium (0.6 M Na(Cl)) at 25°C. The measurements were performed as potentiometric titrations (hydrogen electrode) in which OH− was generated coulometrically. The total concentration of Si(OH)4, B, and log[H+] were varied within the limits 0.00075 B 0.008 M and 2.5 -log[H+] 11.7, respectively. Within these ranges the formation of SiO(OH)3− and SiO2(OH)22− with formation constants log β−11(Si(OH)4 SiO(OH)3− + H+) = −9.472 ±0.002 and log β−21(Si(OH)4 SiO2(OH)22− + 2H+) = −22.07 ± 0.01 was established. With B > 0.003 M polysilicate complexes are formed, however, with -log[H+] 10.7 their formation does not significantly affect the evaluated formation constants. Data were analyzed with the least squares computer program LETAGROPVRID.  相似文献   

11.
The C/N and stable C and N isotope ratios (δ13C, δ15N) of sedimentary and suspended particulate matter were determined in the Schelde Estuary. Suspended matter was divided into 2 to 5 size fractions by centrifugation. Four major pools of organic matter were recognized: riverine, estuarine, marine and terrestrial materials. Terrestrial organic matter (δ13C≈−26‰, δ15N≈3.5‰, C/N≈21) is important for the sedimentary pool, but suspended matter is dominated by the marine (δ13C≈−18‰, δ15N≈9‰, C/N≈8), riverine (δ13C≈−30‰, δ15N≈9‰, C/N≈7.5) and estuarine (δ13C≈−29‰, δ15N≈15‰, C/N≈8) end-members. In the upper estuary, the suspended matter size fractions vary systematically in their carbon and nitrogen biogeochemistry, with the small particles having low C/N ratios, depleted δ13C and enriched δ15N values relative to large particles. Moreover, sedimentary and suspended matter differ significantly in terms of C/N ratios (17 vs. 8.9), δ13C (−26.3 vs. −28.9‰) and δ15N (+6.9 vs. 12.0‰). In the lower estuary, suspended matter fractions are similar and sedimentary and suspended organic matter differ only in terms of δ13C (−23.5 vs. −20.1‰). Our data indicate that autochthonous organic matter contributes significantly to the total suspended matter and that the suspended organic matter composition cannot be explained in terms of conservative mixing of riverine and terrestrial sources on the one hand and marine sources on the other hand.  相似文献   

12.
Gas occurrences consisting of carbon dioxide (CO2), hydrogen sulfide (H2S), and hydrocarbon (HC) gases and oil within the Dodan Field in southeastern Turkey are located in Cretaceous carbonate reservoir rocks in the Garzan and Mardin Formations. The aim of this study was to determine gas composition and to define the origin of gases in Dodan Field. For this purpose, gas samples were analyzed for their molecular and isotopic composition. The isotopic composition of CO2, with values of −1.5‰ and −2.8‰, suggested abiogenic origin from limestone. δ34S values of H2S ranged from +11.9 to +13.4‰. H2S is most likely formed from thermochemical sulfate reduction (TSR) and bacterial sulfate reduction (BSR) within the Bakuk Formation. The Bakuk Formation is composed of a dolomite dominated carbonate succession also containing anhydrite. TSR may occur within an evaporitic environment at temperatures of approximately 120–145 °C. Basin modeling revealed that these temperatures were reached within the Bakuk Formation at 10 Ma. Furthermore, sulfate reducing bacteria were found in oil–water phase samples from Dodan Field. As a result, the H2S in Dodan Field can be considered to have formed by BSR and TSR.As indicated by their isotopic composition, HC gases are of thermogenic origin and were generated within the Upper Permian Kas and Gomaniibrik Formations. As indicated by the heavier isotopic composition of methane and ethane, HC gases were later altered by TSR. Based on our results, the Dodan gas field may have formed as a result of the interaction of the following processes during the last 7–8 Ma: 1) thermogenic gas generation in Permian source rocks, 2) the formation of thrust faults, 3) the lateral-up dip migration of HC-gases due to thrust faults from the Kas Formation into the Bakuk Formation, 4) the formation of H2S and CO2 by TSR within the Bakuk Formation, 5) the vertical migration of gases into reservoirs through the thrust fault, and 6) lateral-up dip migration within reservoir rocks toward the Dodan structure.  相似文献   

13.
A C25 highly branched isoprenoid (HBI) monoene hydrocarbon, designated IP25, has been proposed previously to originate from diatoms living in Arctic sea ice, while the presence of IP25 in sediments has been suggested to be a proxy for the occurrence of former Arctic sea ice. Here, we show that the 13C isotopic composition of IP25 in sea ice, in sediment trap material collected under sea ice, and in high latitude northern sediments, is distinctive (isotopically ‘heavy’) and distinguishable from that of organic matter of planktonic or terrigenous origin. Mean δ13C values for IP25 were − 22.3 ± 0.4‰ (sea ice), − 19.6 ± 1.1‰ (sediment traps) and − 19.3 ± 2.3‰ (sediments). These measurements, therefore, support further the proposed use of IP25 as an Arctic sea ice proxy.  相似文献   

14.
We used stable C and N isotope ratios of tissues from 29 fish species from a large subtropical lagoon in southern Brazil to examine spatial variability in isotopic composition and vertical trophic structure across freshwater and estuarine habitats. Nitrogen isotope ratios indicated a smooth gradation in trophic positions among species, with most fishes occupying the secondary and tertiary consumer level. Fish assemblages showed a significant shift in their carbon isotopic signatures between freshwater and estuarine sites. Depleted carbon signatures (from −24.7‰ to −17.8‰) were found in freshwater, whereas more enriched signatures (from −19.1‰ to −12.3‰) were obtained within the estuarine zone downstream. Based on our survey of the C3 and C4 plants and isotopic values for phytoplankton and benthic microalgae reported for ecosystems elsewhere, we hypothesized that the observed δ13C differences in the fish assemblage between freshwater and estuarine sites is due to a shift from assimilating organic matter ultimately derived from C3 freshwater marsh vegetation and phytoplankton at the freshwater site (δ13C ranging from −25‰ to −19‰), to C4 salt-marsh (e.g. Spartina) and widgeon grass (Ruppia maritima), benthic microalgae and marine phytoplankton at the estuarine sites (from −18‰ to −12‰). Our results suggested that fish assemblages are generally supported by autochthonous primary production. Freshwater fishes that likely were displaced downstream into the estuary during periods of high freshwater discharge had depleted δ13C values that were characteristic of the upper lagoon. These results suggest that spatial foodweb subsidies can occur within the lagoon.  相似文献   

15.
In Fiordland, New Zealand, large volumes of organic matter are deposited into the marine environment from pristine forested catchments. Analyses of δ15N, δ13C and δ34S were employed to determine whether these inputs were contributing to marine food webs via assimilation by common macroinvertebrates inhabiting the inner reaches of the fjords. Terrestrially derived organic matter (TOM) had values of δ15N, δ13C and δ34S that were distinct from other carbon source pools, providing sufficient power to quantify the contribution of TOM to the benthic food web. Isotopic values among macroinvertebrates varied significantly, with consistently low values of δ15N, δ13C and δ34S for the abundant deposit feeders Echinocardium cordatum (Echinodermata) and Pectinaria australis (Annelida), indicating assimilation of TOM. High concentrations of bacterial fatty acid biomarkers in E. cordatum, and values of δ13C of these biomarkers similar to TOM (−27 to −30‰) confirmed that TOM is indirectly assimilated by these sea urchins via heterotrophic bacteria. TOM was also found to enter the infaunal food web via chemoautotrophic bacteria that live symbiotically within Solemya parkinsonii (Bivalvia). Echinocardium cordatum, Pectinaria australis and S. parkinsonii comprised up to 33.5% of the biomass of the macroinfaunal community, and thus represent strong pathways for movement of organic matter from the forested catchments into the benthic food web. This demonstration of connectivity among adjacent marine and terrestrial habitats has important implications for coastal land management, and highlights the importance of intact coastal forests to marine ecosystem function.  相似文献   

16.
The stable carbon isotope composition of particulate organic carbon (POC) from plankton, sediment trap material and surface sediments from the Atlantic sector of the Southern Ocean were determined. Despite low and constant water temperatures, large variations in the δ13C values of plankton were measured. 13C enrichments of up to 10‰ coincided with a change in the diatom assemblage and a two-fold increase in primary production. Increased CO2 consumption as a result of rapid carbon fixation may result in diffusion limitation reducing the magnitude of the isotope fractionation. The δ13C values of plankton from sea-ice cores display a relationship with the chlorophyll a content. High ‘ice-algae’ biomass, in combination with a limited exchange with the surrounding seawater, results in values of about − 18 to − 20‰. It is assumed that these values are related to a reduced CO2 availability in the sea-ice system. In comparison with plankton, sinking krill faeces sampled by traps can be enriched by 2–5‰ in 13C (e.g. central Bransfield Strait). In contrast, the transport of particles in other faeces, diatom aggregates or chains results in minor isotope changes (e.g. Drake Passage, Powell Basin, NW Weddell Sea). A comparison between the δ13C values of sinking matter and those of surface sediments reveals that 13C enrichments of up to 3–4‰ may occur at the sediment-water boundary layer. These isotopic changes are attributed to high benthic respiration rates.  相似文献   

17.
This study examined the relationship between carbon isotopic composition of sinking organic matter (OM) and the biological, physical and chemical properties of the surface ocean in the Cariaco Basin. The 13C/12C ratio of OM (δ13Corg) in sinking particles was determined on sediment trap samples from four depths collected from 1996 to 1999 as part of the CArbon Retention In A Colored Ocean time series. Water column properties, including temperature, productivity, chlorophyll and concentration of dissolved CO2, were concurrently measured on monthly cruises. The δ13Corg varied from a high of –17.7‰ to a low of –22.6‰ during the study period. The variation of the δ13Corg throughout seasonal cycles was directly proportional to the strength of upwelling and was negatively correlated with temperature (r2=0.64). During the 1996–1997 upwelling event, the strongest during the study period, the δ13Corg increased by 4.4‰ whereas during the 1998–1999 upwelling event, the weakest during the study period, the δ13Corg only increased by 3.3‰. Contrary to most previous studies, we observed a negative relationship (r2=0.53) between [CO2 aq] and the estimated isotopic fractionation factor (εp). However, there was no correlation between εp and the calculated growth rates indicating that there was non-diffusive uptake of carbon into phytoplankton cells. It thus appears that [CO2 aq] does not control the δ13Corg in the water column of the study site. The best explanation for the isotopic enrichment observed is a carbon concentrating mechanism (CCM) in phytoplankton. The existence of a CCM in phytoplankton has major implications for the interpretation of the δ13Corg in the Cariaco Basin.  相似文献   

18.
Carbon and nitrogen stable isotope ratios of particulate organic matter (POM) were studied approximately weekly during spring and summer 2003 and 2004 in the Gulf of Trieste (northern Adriatic Sea) in order to track the temporal variations and differences between two years. In parallel, particulate organic carbon (POC) and particulate nitrogen (PN), phytoplankton biomass (chlorophyll a), and N and P nutrients were monitored. All studied parameters, especially N and P nutrients and chlorophyll a, showed higher concentrations and larger variability in spring 2004. As a consequence the macroaggregates were produced in late spring 2004. The C and N isotope composition of POM was not directly linked to phytoplankton biomass dynamics. The δ13CPOC values covaried with temperature. In 2004, δ13CPOC variations followed the δ15NPN values as well as the δ13CDIC values which were probably more dependent on the photosynthetic use of 12C. Variations in δ15NPOM values were most probably the consequence of variations in N nutrient sources used in phytoplankton assimilation. The significant correlation between δ15NPN values and nitrate concentrations in 2004 implies intense nitrate assimilation in the presence of higher nitrate concentration. This suggests nitrate as the key nutrient in the »new primary production«, later producing macroaggregates with a mean δ13C and δ15N values of − 19‰ and 5‰, respectively. A low fractionation factor ε, < 1‰, lower than that reported in other marine and lacustrine systems, was found probably to be a consequence of distinct phytoplankton species, i.e. several classes of autotrophic nanoflagellates, and specific growth conditions present in the Gulf of Trieste. The tentative use of C isotope composition of POM revealed a higher contribution of allochthonous organic matter in 2004 compared to 2003 due to higher riverine inflow.  相似文献   

19.
Extensive artificial waterways have replaced natural wetlands and created new estuarine habitats on the southern Queensland coast, Australia. Economically important fish species found in adjacent natural wetlands of mangrove, saltmarsh and seagrass also occur in the artificial waterways. Stable isotope analyses (δ13C, δ15N) were used to test whether the relative importance of basal sources of energy varied for foodwebs found in artificial (canals and tidal lakes) and natural waterways. None of the fish species differed in their isotope values between artificial waterways. In contrast, isotopic signatures of snub-nosed garfish (Arrhamphus sclerolepis; Hemiramphidae) varied greatly between natural and artificial waterways, having highly enriched δ13C values (−10.5‰) in natural wetlands, demonstrating reliance on seagrass (−11.4‰), and significantly less enriched values (−19.0‰) in artificial waterways, consistent with either local algal sources (−19.8 to −20.4‰) or a mixture of seagrass and other less enriched autotrophs from adjacent natural wetlands. Isotopic signatures of sand whiting (Sillago ciliata; Sillaginidae) were also significantly more enriched in natural (−18.2‰) than artificial (−21.0‰) habitats, but means were not far enough apart to distinguish between different sources of nutrition. δ13C values of yellowfin bream (Acanthopagrus australis; Sparidae) did not differ between artificial and natural habitats (about −20‰ in both). δ15N values of fish varied among habitats only for A. sclerolepis, which in artificial waterways had values enriched by 2‰ over those in natural waterways. This was consistent with a shift from seagrass (relatively depleted δ15N) as a source in natural habitat to algal sources (relatively enriched δ15N) in artificial habitats. This study provides some of the first evidence that at least some fish species rely on different autotrophs in artificial waterways than in adjacent natural wetlands.  相似文献   

20.
Carbon and nitrogen isotopic composition was used to identify the main sources of carbon and describe the main trophic pathways in Deluge Inlet, a near-pristine mangrove estuary in tropical north Queensland, Australia. Producers' δ13C varied from −28.9‰ for mangroves to −18.6‰ for seagrass. Animals were also well separated in δ13C (−25.4‰ to −16.3‰ for invertebrates and −25.2‰ to −17.2‰ for fish), suggesting considerable differences in ultimate sources of carbon, from a substantial reliance on mangrove carbon to an almost exclusive reliance on seagrass. In general, invertebrates had lower δ15N than fish, indicating lower trophic levels. Among fish, δ15N values reflected well the assumed trophic levels, as species from lower trophic levels had lower δ15N than species from higher trophic levels. Trophic levels and trophic length were estimated based on δ15N of invertebrate primary consumers (6.1‰), with results suggesting a food web with four trophic levels. There was also evidence of a high level of diet overlap between fish species, as indicated by similarities in δ13C for fish species of higher trophic levels. Stable isotope data was also useful to construct a general model for this food web, where five main trophic pathways were identified: one based on both mangrove and microphytobenthos, one on plankton, two on both microphytobenthos and seagrass, and one based mainly on seagrass. This model again suggested the presence of four trophic levels, in agreement with the value calculated based on the difference in δ15N between invertebrate primary consumers and top piscivores.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号