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1.
理解早期成岩过程中有机质的化学和同位素分馏对于研究海洋和湖泊环境中的生物地球化学过程是很重要的。将珠江口外近海生物成因有机质分为可水解氨基酸、碳水化合物、脂类和酸不溶四个部分,分析了有机质的化学和同位素组成(δ13C,δ15N),借以讨论沉积有机质在埋藏的早期成岩过程中所发生的化学和同位素改变,结果表明,从浮游生物→悬浮颗粒物→表层沉积物→沉积柱内部,易降解组分可水解氨基酸、碳水化合物、脂类占样品总有机碳的份额依次降低。沉积物及四个有机部分的稳定碳同位素组成在纵向上随深度保持相对恒定,而在不同有机部分之间差异明显。不同类型有机物的分解速率差异在改变有机质化学成分的同时,导致其δ13C发生小幅度负向漂移;细菌有机质的形成和分解对有机质化学成分和同位素组成演化也有重要贡献,并且在一定程度上抵消了上述δ13C的负向漂移,其结果导致沉积有机质的δ13C略低于浮游生物;另一方面,由于异养菌生长过程中的氮同位素分馏系数与可利用氮源的特征和培养基的性质等多种因素有关,导致沉积物的δ15N变化范围增大。在这里δ13C可以可靠地指示该海域沉积有机质的来源,而δ15N变化范围较大且规律不明显,难以用作沉积有机质来源的指示。  相似文献   

2.
珠江口及近海表层沉积有机质的特征和来源   总被引:9,自引:0,他引:9       下载免费PDF全文
测定了珠江口及近海表层沉积物中总有机碳(TOC), 总氮(TN)及稳定碳同位素组成和几类主要有机化合物(水解氨基酸THAA、糖类TCHO、脂类lipid、酸不溶有机物AIOC), 并分析了沉积有机质及化合物的特征和来源。结果表明珠江口表层沉积有机质主要为陆源和水生混合来源, 而近海有机质主要为当地水生来源。大量的陆源高等植物(含有较多的木质素、纤维素等)输入珠江口, 使得珠江口个别站位沉积物中糖类物质含量大幅高于近海样品; 而珠江口与近海沉积物中水生来源有机质的含量相当。氨基酸和糖类占TOC的份额在浮游生物和悬浮颗粒物中分别为56%和48%, 在表层沉积物中为19%, 说明珠江口和近海的有机质从水柱到达沉积物-水界面的过程中经历了较充分的降解。珠江口样品中活性组分氨基酸和糖类占TOC的份额低于近海, 可能说明珠江口沉积有机质的降解程度高于近海。  相似文献   

3.
Relationships between organic carbon, total nitrogen and organic nitrogen concentrations and variations in δ13Corg and δ15Norg are examined in surface sediments from the eastern central Arctic Ocean and the Yermak Plateau. Removing the organic matter from samples with KOBr/KOH and determining residual as well as total N shows that there is a significant amount of bound inorganic N in the samples, which causes TOC/Ntotal ratios to be low (4–10 depending on the organic content). TOC/Norg ratios are significantly higher (8–16). This correction of organic TOC/N ratios for the presence of soil-derived bound ammonium is especially important in samples with high illite concentrations, the clay mineral mainly responsible for ammonium adsorption. The isotopic composition of the organic N fraction was estimated by determining the isotopic composition of the total and inorganic nitrogen fractions and assuming mass-balance. A strong correlation between δ15Norg values of the sediments and the nitrate concentration of surface waters indicates different relative nitrate utilization rates of the phytoplankton in various regions of the Arctic Ocean. On the Yermak Plateau, low δ15Norg values correspond to high nitrate concentrations, whereas in the central Arctic Ocean high δ15Norg values are found beneath low nitrate waters. Sediment δ13Corg values are close to −23.0‰ in the Yermak Plateau region and approximately −21.4‰ in the central Arctic Ocean. Particulate organic matter collected from meltwater ponds and ice-cores are relatively enriched in 13C (δ13Corg=−15.3 to −20.6‰) most likely due to low CO2(aq) concentrations in these environments. A maximum terrestrial contribution of 30% of the organic matter to sediments in the central Arctic Ocean is derived, based on the carbon isotope data and various assumptions about the isotopic composition of the potential endmembers.  相似文献   

4.
The role of the Setúbal–Lisbon canyon in accumulation and transport of labile organic matter from the coastal sea and ocean surface water towards the deep sea was assessed by investigating the distribution of organic matter of different quality in sedimentary aggregates and surface sediments of the canyon and adjacent slopes. Total hydrolysable amino acids (THAA) and organic carbon (Corg) were measured from aggregates, and contents of Corg, chlorophyll a (chl a), phaeopigments (phaeo), chloroplastic pigment equivalents (CPE) from sediments. As indices of organic matter (OM) quality THAA:Corg, degradation index (DI), chl a:phaeo, chl a:Corg and C:N ratio were determined. Sediment profiles of chl a and the isotope 210 of lead (210Pb) were used as tracers in a transport model to estimate deposition rates and background levels of the tracers, and sediment mixing rates (Db). Whereas bulk Corg contents of canyon and slope sediments were practically similar at all depths, higher contents of THAA, chl a and CPE, as well as higher THAA:Corg, DI and chl a:Corg, in aggregates and sediments from the upper reaches of the canyon indicate that labile organic matter accumulates in the upper canyon. This is confirmed by higher chl a and 210Pb deposition and Db calculated from the model. Hence, the Setúbal–Lisbon canyon, specially the upper region, acts as a natural trap of organic matter that is transported to the region via lateral transport and vertical settling from primary productivity. Organic matter might be further transported in downward canyon direction via rebound processes. The chl a and 210Pb profiles reveal active sediment mixing by physical processes and/or animal reworking.  相似文献   

5.
Settling particles and surface sediments collected from the western region of the Sea of Okhotsk were analyzed for total organic carbon (TOC), long-chain n-alkanes and their stable carbon isotope ratio (δ13C) to investigate sources and transport of total and terrestrial organic matter in the western region of the sea. The δ13C measurements of TOC in time-series sediment traps indicate lateral transport of resuspended organic matter from the northwestern continental shelf to the area off Sakhalin via the dense shelf water (DSW) flow at intermediate depth. The n-alkanes in the surface sediments showed strong odd carbon number predominance with relatively lighter δ13C values (from −33‰ to −30‰). They fall within the typical values of C3-angiosperms, which is the main vegetation in east Russia, including the Amur River basin. On the other hand, the molecular distributions and δ13C values of n-alkanes in the settling particles clearly showed two different sources: terrestrial plant and petroleum in the Sea of Okhotsk. We reconstructed seasonal change in the fluxes of terrestrial n-alkanes in settling particles using the mixing model proposed by Lichtfouse and Eglinton [1995. 13C and 14C evidence of a soil by fossil fuel and reconstruction of the composition of the pollutant. Organic Geochemistry 23, 969–973]. Results of the terrestrial n-alkane fluxes indicate that there are two transport pathways of terrestrial plant n-alkanes to sediments off Sakhalin, the Sea of Okhotsk. One is lateral transport of resuspended particles with lithogenic material from the northwestern continental shelf by the DSW flow. Another is the vertical transport of terrestrial plant n-alkanes, which is independent of transport of lithogenic material. The latter may include dry/wet deposition of aerosol particles derived from terrestrial higher plants possibly associated with forest fires in Siberia.  相似文献   

6.
Several chemical markers of organic matter source and age are shown to be susceptible to light-induced alteration. To test for the photochemical lability of markers previously employed for sediments from the Louisiana coastal zone, we subjected sediments under resuspension conditions to simulated sunlight, and monitored changes in C:N and Br:OC ratios, δ13C, Δ14C, and lignin composition. Markers of terrigenous origin (high C:N, lignin) decreased and δ13C became enriched in sediments containing primarily terrigenous organic matter, while a marker of marine organic matter (Br:OC) decreased in samples containing significant contributions from this source. Preferential loss of 14C from all sediments indicated enhanced photochemical lability of organic matter of relatively recent origin, consistent with the changes in chemical markers. Most, but not all, experimental alterations are consistent with field distributions of these markers. Relatively small experimental changes in the markers in combination with confounding processes in the environment, however, prevent these parallel trends from providing any more than a consistency test for the importance of photochemical reactions in this region.  相似文献   

7.
Six sediment cores collected from various water depths and sampling locations along the western margin of the Bay of Bengal (BOB) were investigated for the total hydrolysable amino acids (THAA) and d-amino acids (d-AA) to understand their distribution, digenetic alteration and bacterial contribution to organic matter (OM). Irrespective of their location, THAA concentrations and yields generally decreased and mol% glycine increased with increasing water depth indicating that OM was degraded during its transit through the water column. Amino acid based degradation index (DI) indicated that OM of the surface sediments of shallow stations, BOB-1 to BOB-3 was relatively fresher than that of deeper stations, BOB-4, BOB-5 and BOB-6. The concentrations and mol% of the d-AA varied from 0.04 to 0.76 µmol gdw−1 and 0.3 to 8.5 mol%, respectively. Contribution of bacterial peptidoglycan amino acids to THAA (% THAApep/THAA) ranged between 4.0% and 55.0%. Both % THAApep/THAA and mol% d-AAs were significantly (p<0.01) higher in the surface sediments and decreased with sediment core depth. Based on the d-AA yields, bacterial OM accounted for 1.5–15.6% of TOC, and 3.7–50.0% of TN of the sediments of BOB.  相似文献   

8.
The Jiaozhou Bay is characterized by heavy eutrophication that is associated with intensive anthropogenic activities. Four core sediments from the Jiaozhou Bay are analyzed using bulk technologies, including sedimentary total organic carbon(TOC), total nitrogen(TN), the stable carbon(δ~(13)C) and nitrogen(δ~(15) N) isotopic composition to obtain the comprehensive understanding of the source and composition of sedimentary organic matter and further shed light on the environmental changes of the Jiaozhou Bay on a centennial time scale.Results suggest that the TOC and TN concentrations increase in the upper core, having indicated a probable eutrophication process since the 1920 s in the inner bay and the 2000 s in the bay mouth. The TOC and TN concentrations outside the bay have also changed since 1916 owing to the variation of terrigenous input.Considering TOC/TN ratio, δ~(13) C and δ~(15) N, it can be concluded there is a mixture of terrigenous and marine organic matter sources in the study area. A simple two end-member(terrigenous and marine) mixing model usingδ~(13) C indicats that 45%–79% of TOC in the Jiaozhou Bay is from the marine source. The environmental changes of the Jiaozhou Bay are recorded by geochemical proxies, which are influenced by the intensive anthropogenic activities(e.g., extensive use of fertilizers, and discharge of sewage) and climate changes(e.g., rainfall).  相似文献   

9.
Total hydrolysable amino acids (THAA), individual amino acid distributions, total organic carbon (TOC) and total nitrogen (TN) were measured in sediments across the Goban Spur continental slope at water depths of 651, 1296 and 3650 m. Objectives were to examine (1) differences in organic matter (OM) degradation state in surface sediments across the slope from sedimentary amino acid compositions, and (2) whether these differences are related to particle size distributions. Application of a ‘reaction–diffusion’ model to the sediment concentration profiles showed that TOC and THAA degradation rate constants decreased with increasing water depth. Ratios of degradation rate constants of THAA over TOC indicated that THAA turn over faster than TOC at 651 and 1296 m water depth only. From estimates of degradation rate constants of individual amino acids, it was concluded that with increasing water depth fewer amino acids contribute to overall THAA degradation. The contribution of THAA to TOC mineralisation decreased from the upper to the lower slope. Since at all three sampling stations the amino acids with the highest relative contribution to THAA had a higher abundance in sediments with reduced THAA mineralisation rates, we conclude that the overall amino acid reactivity decreases with increasing water column depth. A principal component analyses, carried out on normalised amino acid mole percentages, established significant shifts in amino acid compositions and confirmed that (1) OM degradation state increased from 651 to 3650 m and (2) that OM in the finest fraction at the shallowest station appeared to be considerably less degraded than in the coarser fractions or any size fractions at the deeper stations. Therefore, we conclude that downslope transport, sorting and accumulation of fine particles with continuous mineralisation of OM attached to the particles during vertical and lateral transport results in an increasing organic matter degradation state from the upper slope to the abyssal plain.  相似文献   

10.
To establish the relative importance of terrigenous and marine organic matter in the southern Beaufort Sea, we measured the concentrations and the stable isotopic compositions of organic carbon and total nitrogen in sediments and in settling particles intercepted by sediment traps. The organic carbon content of surface sediment in the Chukchi and southern Beaufort Seas ranged from 0.6 to 1.6% dry wt., without a clear geographical pattern. The CORG:NTOT ratio ranged from 7.0 to 10.4 and did not vary significantly downcore at any one station. Values of δ13CORG and δ15NTOT in the sediment samples were strongly correlated, with the highest values, indicative of a more marine contribution, in the Amundsen Gulf. In contrast, the organic matter content, elemental (CORG:NTOT ratio) and isotopic (δ13CORG and δ15NTOT) composition of the settling particles was different from and much more variable than in the bottom sediments. The isotopic signature of organic matter in the Beaufort Sea is well constrained by three distinct end-members: a labile marine component produced in situ by planktonic organisms, a refractory marine component, the end product of respiration and diagenesis, and a refractory terrigenous component. A three-component mixing model explains the scatter observed in the stable isotope signatures of the sediment trap samples and accommodates an apparent two-component mixing model of the organic matter in sediments. The suspended matter in the water column contains organic matter varying from essentially labile and marine to mostly refractory and terrigenous. As it settles through the water column, the labile marine organic matter is degraded, and its original stable isotope signature changes towards the signature of the marine refractory component. This process continues in the bottom sediment with the result that the sedimentary organic matter becomes dominated by the refractory terrigenous and marine components.  相似文献   

11.
We have conducted elemental, isotopic, and Rock-Eval analyses of Cenomanian–Santonian sediment samples from ODP Site 1138 in the southern Indian Ocean to assess the origin and thermal maturity of organic matter in mid-Cretaceous black shales found at this high-latitude location. Total organic carbon (TOC) concentrations range between 1 and 20 wt% in black to medium-gray sediments deposited around the Cenomanian–Turonian boundary. Results of Rock-Eval pyrolysis indicate that the organic matter is algal Type II material that has experienced modest alteration. Important contributions of nitrogen-fixing bacteria to the amplified production of organic matter implied by the high TOC concentrations is recorded in δ15N values between −5 and 1‰, and the existence of a near-surface intensified oxygen minimum zone that favored organic carbon preservation is implied by TOC/TN ratios between 20 and 40. In contrast to the marine nature of the organic matter in the Cenomanian–Turonian boundary section, deeper sediments at Site 1138 contain evidence of contributions land-derived organic matter that implies the former presence of forests on the Kerguelen Plateau until the earliest Cenomanian.  相似文献   

12.
通过对南海北部夏、冬两个季节的生源要素垂直输运剖面和时间系列沉积物捕获器的测量资料进行综合研究表明:南海北部颗粒物质主要是由钙质生物壳、生物硅、海洋浮游生物的有机质以及岩源物质组成,颗粒物质通量在1 000 m处大约为90.0 mg/(m2·d);研究还表明颗粒有机碳在进入沉积物保存之前被大量溶解,南海北部来自底层顺坡搬运的有机碳远大于垂直沉降;与开阔大洋(东太平洋海域)的对比研究表明,边缘海对于季节的变化更加敏感,而东太平洋调查区位于热带赤道高生产力带,生物作用十分明显,其海洋生物呼吸和物质转移同样也较活跃.  相似文献   

13.
Sinking particles were analyzed for their nitrogen isotopic ratio δ15N) of total particulate nitrogen (PN), stable carbon isotopic ratio (δ13C) and radioactive isotopic ratio (δ14C) of total particulate organic carbon (POC), at three different latitudinal (temperate, subpolar and equatorial) and geomorphological (trench, proximal abyssal plain and distal abyssal plain) sites in the western North Pacific Ocean using year-long time series sediment trap systems, to clarify the common vertical trends of the isotopic signals in deep water columns. Although the δ15N and δ13C values of sinking particulate organic matter (POM) were partly affected by the resuspension of sedimentary POM from the sea floor, especially in the trench, the changes in δ15N and δ13C values owing to the resuspension could be corrected by calculation of the isotopic mass balance from δ14C of sinking POC. After this correction, common downward decreasing trends in δ15N and δ13C values were obtained in the deep water columns, irrespective of the latitudes and depths. These coincidental isotopic signals between δ15N and δ13C values provide new constraints for the decomposition process of sinking POM, such as the preferential degradation of 15N- and 13C-rich compounds and the successive re-formation of the sinking particles by higher trophic level organisms in the deep water column.  相似文献   

14.
《Marine Chemistry》2005,93(1):53-73
The provenance of organic matter in sediments from the Mackenzie River and Beaufort Shelf was investigated using the stable carbon and radiocarbon isotopic compositions of bulk organic matter and the stable carbon isotopic compositions of individual organic compounds, including lignin-derived phenols and lipid-derived fatty acids. Most river suspended sediments and shelf surface sediments contained organic carbon characterized by highly depleted Δ14C values that were consistent with average radiocarbon ages exceeding 7000 years. The stable carbon isotopic signatures of lignin phenols were uniformly depleted (−25≥δ13C≥−32‰), indicating the predominant contributions of C3 vascular plant sources. The isotopic compositions of C14 and C16 fatty acids exhibited important contrasts between the river (−36‰ to −40‰) and shelf (−25‰ to −29‰) sediments that were consistent with contributions from freshwater algae and/or vascular plants in the former and marine phytoplankton in the latter. Using 14C isotopic mass balance, the abundances of modern and ancient organic matter were quantitatively constrained. The fate of organic matter in the Beaufort Shelf was explored by normalizing these abundances to the specific surface area of sediments. Ancient organic carbon, which may include old pre-aged soil material as well as fossil bitumen or kerogen, accounted for the majority (∼70%) of the particulate organic matter exported by the Mackenzie River and deposited in surface sediments of the Beaufort Shelf. Modern organic carbon accounted for ∼30% in both river and shelf sediments, with significant contributions from vascular plant-derived materials in both river and shelf samples and from marine algae in the shelf sediments. Respiration (and/or leaching) of particle-bound marine organic matter dominates the carbon metabolism in the Mackenzie Delta/Beaufort Shelf region. However, land-derived pools, including modern carbon derived from vascular plants as well as ancient carbon also appeared to undergo a degree of post-depositional degradation prior to burial in the shelf. These novel source apportionments are reflected in an updated carbon budget for the study area.  相似文献   

15.
Evidence from geochemical tracers (salinity, oxygen, silicate, nutrients, alkalinity, dissolved inorganic carbon (DIC), carbon isotopes (δ13CDIC) and radiocarbon (Δ14C)) collected during the Pacific Ocean World Ocean Circulation Experiment (WOCE) voyages (P10, P15, P17 and P19) indicate there are three main water types at intermediate depths in the Pacific Ocean; North Pacific Intermediate Water (NPIW), Antarctic Intermediate Water (AAIW) and Equatorial Pacific Intermediate Waters (EqPIW). We support previous suggestions of EqPIW as a separate equatorial intermediate depth water as it displays a distinct geochemical signature characterised by low salinity, low oxygen, high nutrients and low Δ14C (older radiocarbon). Using the geochemical properties of the different intermediate depth waters, we have mapped out their distribution in the main Pacific Basin.From the calculated pre-formed δ13Cair–sea conservative tracer, it is evident that EqPIW is a combination of AAIW parental waters, while quasi-conservative geochemical tracers, such as radiocarbon, also indicate mixing with old upwelling Pacific Deep Waters (PDW). The EqPIW also displays a latitudinal asymmetry in non-conservative geochemical tracers and can be further split into North (NEqPIW) and South (SEqPIW) separated at ~2°N. The reason for this asymmetry is caused by higher surface diatom production in the north driven by higher silicate concentrations.The δ13C signature measured in benthic foraminifera, Cibicidoides spp.13CCib), from four core tops bathed in AAIW, SEqPIW and NPIW, reflects that of the overlying intermediate depth waters. The δ13CCib from these cores show similarities and variations down-core that highlight changes in mixing over the last 30,000 yr BP. The reduced offset between the δ13CCib of AAIW and SEqPIW during the last glacial indicates that AAIW might have had an increased influence in the eastern equatorial Pacific (EEP) region at this time. Additional intermediate depth cores and other paleo-geochemical proxies such as Cd/Ca and radiocarbon are required from the broader Pacific Ocean to further understand changes in intermediate depth water formation, circulation and mixing over glacial/interglacial cycles.  相似文献   

16.
鸭绿江河口西岸潮滩沉积物有机质对流域变化的响应   总被引:1,自引:1,他引:0  
河流颗粒有机质提供了陆地碳循环的重要信息以及人类活动的记录,通过河口地区沉积物有机质组成,可反映流域变化及海陆间相互作用。2010-2011年分两次于鸭绿江河口西岸潮滩采集柱样4根及表层样23个。对样品进行有机质碳氮总量(TOC、TN)、碳氮同位素(δ13C、δ15 N)及沉积物粒度测试。分析结果表明,由河口向西,有机质受改造程度加深且来源逐渐复杂化,致TOC/TN与δ13C的相关性逐渐降低,δ15 N与沉积物粒度的相关性也随之降低。文中以δ13C为主线探讨沉积物有机质的来源及运移,TOC/TN作为辅助,δ15 N则用于指示生化条件的改变。柱样的δ13 C分布与河流入海输沙密切相关,水库对入海泥沙的拦截,致河口潮滩沉积速率减缓,从而增加了沉积物中海源有机质的含量,δ13C随之增加。潮滩西侧柱样的δ15 N增加指示了生活工业污水的大量排放。此外,表层样δ13C分布的方向性,指示了西水道门口处的快速堆积及潮下带物质的向岸运移,并在西岸潮滩向岸一侧富集。  相似文献   

17.
Oxygen and carbon isotopes (δ18O and δ13C) have been investigated in carbonate tests of deep-sea foraminifera living in the Mozambique Channel (eastern Africa) to understand how environmental constraints (e.g., organic matter, oxygenation) control the intra- and interspecific variability of isotopic signatures. 197 living individuals, including eight different species, from various microhabitats within the sediment were sorted from sediment samples gathered at two stations on the Malagasy upper slope. Results show that the δ18O values of foraminiferal taxa were not controlled by microhabitat pattern. They presented tremendous and intriguing intraspecific variability that is not explained by the classical ontogenetic effect. The δ13C values of infaunal foraminiferal taxa do not show a 1:1 relationship with the bottom water δ13C DIC and do not present a constant offset from it; instead, they appear to be mainly controlled by a microhabitat effect. The lower δ13C values of shallow, intermediate, and deep infaunal taxa at the deeper station compared to those seen at the shallower station reflect the enhanced exportation of sedimentary organic matter at the sediment–water interface, and its related mineralization within the upper sediments. The ?δ13C between shallow/very shallow infaunal species (i.e., Hoeglundina elegans, Uvigerina hispida) and intermediate/deep infaunal species (i.e., Melonis barleeanus, Globobulimina barbata) permits insight into (1) the exportation of organic matter to the seafloor and (2) the various degradation pathways for organic detritus in the benthic environments off NW Madagascar.  相似文献   

18.
The nitrogen isotopic composition of time-series sediment trap samples, dissolved NO-3, and surficial sediments was determined in three regions along the margin of the eastern North Pacific: Monterey Bay, San Pedro Basin, and the Gulf of California (Carmen and Guaymas Basins). Complex physical regimes are present in all three areas, and each is influenced seasonally by coastal upwelling. Nevertheless, sediment trap material evidently records the isotopic composition of new nitrogen sources, since average δ15N is generally indistinguishable from δ15N values for subsurface NO-3. Surficial sediments are also very similar to the average δ15N value of the sediment traps, being within 1‰. This difference in δ15N between trap material and sediment is much less than the previously observed 4‰ difference for the deep sea. Better organic matter preservation at our margin sites is a likely explanation, which may be due to either low bottom O2 concentrations or higher organic matter input to the sediments. All sites have δ15N for sub-euphotic zone NO-3 (8–10‰) substantially elevated from the oceanic average (4.5–5‰). This isotopic enrichment is a result of denitrification in suboxic subsurface waters (Gulf of California) or northward transport of denitrification influenced water (Monterey Bay and San Pedro Basin). Our results therefore suggest that downcore δ15N data, depending on site location, would record the intensity of denitrification and the transport of its isotopic signature along the California margin. Temporal variations in δ15N for the sediment traps do appear to respond to upwelling or convective injections of NO-3 to surface waters as a result of isotopic fractionation during phytoplankton uptake. Overall, though, the coupling between NO-3 injection, δ15N, and flux is looser than previously observed for the open-ocean, most likely the result of the smaller time/space scales of the events. In the Gulf of California, wintertime convective mixing/upwelling does produce distinct δ15N minima co-occurring with particle flux maxima. Interannual variations are apparent in this region when these winter-time δ15N minima fail to occur during El Niño conditions. There appears to be a positive relationship between the Southern Oscillation Index (SOI) anomaly and annual average δ15N. One explanation calls for hydrographic changes altering the δ15N of subeuphotic zone NO-3.  相似文献   

19.
Incorporation of 14C-depleted (old) dissolved organic carbon (DOC) on/into particulate organic carbon (POC) has been suggested as a possible mechanism to explain the low Δ14C-POC values observed in the deep ocean [Druffel, E.R.M., Williams, P.M., 1990. Identification of a deep marine source of particulate organic carbon using bomb 14C. Nature, 347, 172–174.]. A shipboard incubation experiment was performed in the Sargasso Sea to test this hypothesis. Finely ground dried plankton was incubated in seawater samples from the deep Sargasso Sea, both with and without a biological poison (HgCl2). Changes in parameters such as biochemical composition and carbon isotopic signatures of bulk POC and its organic compound classes were examined to study the roles of sorptive processes and biotic activity on POC character. Following a 13-day incubation, the relative abundance of the acid-insoluble organic fraction increased. Abundances of extractable lipids and total hydrolyzable amino acids decreased for both treatments, but by a greater extent in the non-poisoned treatment. The Δ14C values of POC recovered from the non-poisoned treatment were significantly lower than the value of the unaltered plankton material used for the incubation, indicating incorporation of 14C-depleted carbon, most likely DOC. The old carbon was present only in the lipid and acid-insoluble fractions. These results are consistent with previous findings of old carbon dominating the same organic fractions of sinking POC from the deep Northeast Pacific [Hwang, J., Druffel, E.R.M., 2003. Lipid-like material as the source of the uncharacterized organic carbon in the ocean? Science, 299, 881–884.]. However, the Δ14C values of POC recovered from the poisoned treatment did not change as much as those from the non-poisoned treatment suggesting that biological processes were involved in the incorporation of DOC on/into POC.  相似文献   

20.
N. A. Shulga 《Oceanology》2018,58(5):672-678
This work presents the first results of a comparative study on the composition and distribution of organic matter (OM) (TOC, n-alkanes, pristane, phytane) in ferromanganese nodules and underlying sediments (0–1 cm) from three sites within the Clarion–Clipperton Fracture Zone, Pacific Ocean. Samples were collected during Cruise 120 of the RSS James Cook in 2015. The studied nodules differ in size, shape, and morphology. The TOC content in the nodules is 0.15% on average with insignificant variations which is less than in the sediments. The molecular composition of n-alkanes in the nodules is mainly determined by modern bacterial activity with high preservation of terrigenous n-alkanes in the environment of the ore deposit formation.  相似文献   

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