Potential source and diagenetic signatures of oceanic dissolved and particulate organic matter as distinguished by lipid biomarker distributions   总被引：1，自引：0，他引：1  

Ai Ning Loh  Elizabeth A. Canuel  James E. Bauer   《Marine Chemistry》2008,112(3-4):189-202

Potential biogenic sources of ultrafiltered dissolved and suspended particulate organic matter (UDOM and POM, respectively) from the Sargasso Sea (SS) and North Central Pacific (NCP) Ocean were investigated using lipid biomarker compounds. Organic carbon (OC) concentrations were ~ 20–40 times greater in UDOM than POM and decreased with depth. However, total OC-normalized lipid concentrations were 2–3 orders of magnitude higher in POM than in UDOM. Particulate total lipids decreased 3–10-fold with depth, compared to 10–20% for dissolved total lipids. Total fatty acids (FA), the most abundant lipids, showed similar patterns as total lipids, comprising ~ 62–88% of the total lipids analyzed in UDOM and ~ 57–84% in POM.FA were dominated by straight-chain saturated compounds followed by monounsaturated, polyunsaturated, and branched FA. Polyunsaturated FA were enriched in POM vs. UDOM and in surface vs. deep waters for both UDOM and POM, likely reflecting the algal origins and greater reactivity of surface-derived materials. In both UDOM and POM, sterols of planktonic origin dominated, including cholest-5-en-3β-ol (C₂₇Δ⁵), 24-methylcholesta-5,24(28)E-dien-3β-ol (C₂₈Δ^5,24(28)) and 24-ethylcholest-5-3β-ol (C₂₉Δ⁵), with varying contributions from cholesta-5,22E-3β-ol (C₂₇Δ^5,22), 24-methylcholesta-5,22E-3β-ol (C₂₈Δ^5,22) and 24-ethylcholesta-5,22E-3β-ol (C₂₉Δ^5,22).Factor analysis of lipid biomarkers showed major differences between the UDOM and POM pools and for each pool as a function of depth, but not between the SS and NCP. While UDOM and POM biomarkers were both dominated by autochthonous sources, differences between the two pools suggest potential effects from some combination of source and diagenetic factors. The lipid biomarker data are further evaluated relative to previous studies of radiocarbon (¹⁴C) and elemental (C:N:P) characteristics of UDOM and POM in the SS and NCP.  相似文献   

Sources and transport of dissolved and particulate organic carbon in the Mississippi River estuary and adjacent coastal waters of the northern Gulf of Mexico   总被引：5，自引：0，他引：5  

Xu-Chen Wang  Robert F. Chen  George B. Gardner 《Marine Chemistry》2004,89(1-4):241

Dissolved organic carbon (DOC), stable carbon isotopic (δ¹³C) compositions of DOC and particulate organic carbon (POC), and elemental C/N ratios of POC were measured for samples collected from the lower Mississippi and Atchafalaya rivers and adjacent coastal waters in the northern Gulf of Mexico during the low flow season in June 2000 and high flow season in April 2001. These isotopic and C/N results combined with DOC measurements were used to assess the sources and transport of terrestrial organic matter from the Mississippi and Atchafalaya rivers to the coastal region in the northern Gulf of Mexico. δ¹³C values of both POC (−23.8‰ to −26.8‰) and DOC (−25.0‰ to −29.0‰) carried by the two rivers were more depleted than the values measured for the samples collected in the offshore waters. Strong seasonal variations in δ¹³C distributions were observed for both POC and DOC in the surface waters of the region. Fresh water discharge and horizontal mixing played important roles in the distribution and transport of terrestrial POC and DOC offshore. Our results indicate that both POC and DOC exhibited non-conservative behavior during the mixing especially in the mid-salinity range. Based on a simple two end-member mixing model, the comparison of the measured DOC-δ¹³C with the calculated conservative isotopic mixing curve indicated that there was a significant in situ production of marine-derived DOC in the mid- to high-salinity waters consistent with our in situ chlorophyll-a measurements. Our DOC-δ¹³C data suggest that a removal of terrestrial DOC mainly occurred in the high-salinity (>25) waters during the mixing. Our study indicates that the mid- to high- (10–30) salinity range was the most dynamic zone for organic carbon transport and cycling in the Mississippi River estuary. Variability in isotopic and elemental compositions along with variability in DOC and POC concentrations suggest that autochthonous production, bacterial utilization, and photo-oxidation could all play important roles in regulating and removing terrestrial DOC in the northern Gulf of Mexico and further study of these individual processes is warranted.  相似文献   

The chemical and physical characteristics of heavy metals in humus and till in the vicinity of the base metal smelter at Flin Flon, Manitoba, Canada   总被引：1，自引：0，他引：1  

P. J. Henderson  I. McMartin  G. E. Hall  J. B. Percival  D. A. Walker 《Environmental Geology》1998,34(1):39-58

 Trace element geochemistry of humus (<0.425 mm) and till (<0.002 mm) collected in the Flin Flon-Snow Lake area, northern Manitoba and Saskatchewan, provides a regional context for assessing smelter contamination in the environment. The area includes a Cu-Zn smelter known to discharge As, Cd, Cu, Fe, Hg, Pb, and Zn. In this study, sequential extraction analyses, scanning electron microscopy and x-ray diffraction analyses were used on a suite of samples to determine: (1) the chemical and physical characteristics of heavy metals in surficial sediments related to distance from the smelter, (2) criteria for assessing the relative contribution of these metals from natural and anthropogenic sources, and (3) the potential of these metals for remobilization in the environment. Humus geochemistry reflects the anthropogenic and natural component of heavy metal concentrations. Smelter-related elements show anomalously high values adjacent to the smelter, decreasing with distance until background values are reached at 70–104 km, depending on the element. In humus, Zn is associated primarily with labile phases; Hg with non-labile phases. Adjacent to the smelter, high proportions and concentrations of Zn and Hg in non-labile phases, indicative of smelter-derived particulates, are confirmed by SEM examination. The particles occur as spheres, irregular grains, and with organics. With increasing distance from the smelter, the geochemical response to bedrock composition is more obvious than the anthropogenic input. Till geochemistry reflects the natural variation imposed by bedrock composition. At highly contaminated sites (<3 km from the smelter), increased percentages of smelter-related elements in labile phases suggests heavy metals are leached from humus to the underlying sediment. Received: 5 November 1996 · Accepted: 31 March 1997  相似文献   

Geochemical characteristics of particulate matter in the atmosphere surrounding a ceramic industrialized area   总被引：3，自引：0，他引：3  

E.?T.?Gómez  T.?Sanfeliu  M.?M.?JordánEmail author  J.?Rius  C.?de la?Fuente 《Environmental Geology》2004,45(4):536-543

Total suspended particulate samples (TSP) were collected and concentrations measured during seventeen months in the vicinity of a ceramic industrial area. A method of fractionating was applied to the samples in order to obtain two fractions corresponding to mineral particulate coming from dust emissions (Upper-F fraction) and to amorphous matter (carbon plus small amounts of S, Ca, Fe, etc) coming mainly from traffic and other combustion processes. Also for TSP samples several element concentrations were measured following two previous treatments: extraction of elements mainly associated with the soluble fraction of the samples (B, Fe, P, As, NO^2–, NH⁴⁺, Cl^–, F) and acid digestion for trace metals and elements mainly associated with the non-soluble fractions of the samples (Fe, As, Cd, Ni, Pb, Zn Ca). Seasonal differences and the influence of meteorological parameters (temperature, relative humidity, pressure and wind conditions) on the air pollution levels, particles as well as ions, were studied.Results show different seasonal and weekly evolution for mineral and amorphous carbonaceous particles because of the different origins in dust emissions or combustion processes respectively, and the different physical properties such as size grain. Of the ions analyzed Fe, Ca and Zn were clearly associated to mineral phases and consequently related to dust emissions, and NO^2–, NH4+, P, Cl^– were related to amorphous matter coming from combustion. Ni and Cd show lower levels than those reported as guideline values and the source is mainly related to the enrichment of these elements in clay materials. B and As content result in elevated concentrations, with the tendency to increase during cold months. The emission of these elements was associated with vaporization or volatilization during high temperature ceramic processes. The original gaseous state is influenced by temperature. In the winter the content for B and As is higher due to enhanced condensation of gas-phase boron onto particles, while in the summer the increase of air temperature results in elevated evaporation.  相似文献   

Phosphorus distribution in sinking oceanic particulate matter   总被引：2，自引：1，他引：2  

Kristina L. Faul  Adina Paytan  Margaret L. Delaney 《Marine Chemistry》2005,97(3-4):307-333

Despite the recognition of the importance of phosphorus (P) in regulating marine productivity in some modern oceanic systems and over long timescales, the nature of particulate P within the ocean is not well understood. We analyzed P concentration in particulate matter from sediment traps and selected core tops from a wide range of oceanic regimes: open ocean environments (Equatorial Pacific, North Central Pacific), polar environments (Ross Sea, Palmer Deep), and coastal environments (Northern California Coast, Monterey Bay, Point Conception). These sites represent a range of productivity levels, temporal (seasonal to annual) distributions, and trap depths (200–4400 m). P associations were identified using an operationally defined sequential extraction procedure. We found that P in the sediment traps is typically composed of reactive P components including acid-insoluble organic P ( 40%), authigenic P ( 25%), and oxide associated and/or labile P ( 21%), with lesser proportions of non-reactive detrital P depending on location ( 13%). The concentrations and fluxes of all particulate P components except detrital P decrease or remain constant with depth between the shallowest and the deepest sediment traps, indicating some regeneration of reactive P components. Transformation from more labile forms of P to authigenic P is evident between the deepest traps and core top sediments. Although for most sites the magnitudes of reactive P fluxes are seasonally variable and productivity dependent, the fractional associations of reactive P are independent of season. We conclude that P is transported from the upper water column to the sediments in various forms previously considered unimportant. Thus, acid-insoluble organic P measurements (typically reported as particulate organic P) likely underestimate biologically related particulate P, because they do not include the labile, oxide-associated, or authigenic P fractions that often are or recently were biologically related. Organic C to reactive P ratios are typically higher than Redfield Ratio and are relatively constant with depth below 300 m suggesting that preferential regeneration of P relative to C occurs predominantly at shallow depths in the water column, but not deeper in the water column (> 300 m). The view of P cycling in the oceans should be revised (1) to include P fractions other than acid-soluble organic P as important carriers of reactive P in rapidly sinking particles, (2) to include the efficient transformation of labile forms of P to authigenic P in the water column as well as in sediments, and (3) to consider the occurrence of preferential P regeneration at very shallow depths.  相似文献   

Particulate barium fluxes on the continental margin: a study from the Alboran Sea (Western Mediterranean)     

Anna Sanchez-Vidal  Robert W. Collier  Antoni Calafat  Joan Fabres  Miquel Canals 《Marine Chemistry》2005,93(2-4):105-117

Particulate biogenic barium (bio-Ba) fluxes obtained from three instrumented arrays moored in the Alboran Sea, the westernmost basin in the Mediterranean Sea, are presented in this study. The mooring lines were deployed over almost 1 year, from July 1997 to May 1998, and were equipped with sediment traps at 500–700 m depth, 1000–1200 m depth and 30 m above the seafloor (1000–2200 m). The results obtained support the growing body of evidence that the relationship between particulate bio-Ba and Corg throughout the water column in margin systems is clearly different from this relation in the open ocean. In the Alboran Sea, the annual averaged bio-Ba fluxes range from 0.39 to 1.07 μmol m⁻² day⁻¹, with mean concentrations of 1.31–1.69 μmol g⁻¹ and bio-Ba/Corg ratios lower than in the open ocean. The low bio-Ba values obtained also indicate that calculating bio-Ba is extremely sensitive to the detrital Ba/Al ratio of each sample. The lithogenic Ba fraction in the Alboran Sea continental margin area contributes between 24% and 85% of the total Ba. Increased bio-Ba export efficiency was observed after periods of high primary productivity and suggests that the processes limiting the bio-Ba formation in the study area relate to settling dynamics of organic matter aggregates. Furthermore, the ballasting effect of the abundant lithogenic and carbonate particles may limit decomposition of organic matter aggregates and enhance the transfer of particles rich in Corg and relatively poor in bio-Ba to the deep seafloor. Lateral input of freshly sedimented biogenic material, including particulate bio-Ba, has been observed on the lower continental slope in the western Alboran Sea. These observations emphasize that the use of the bio-Ba as a proxy of export productivity from the surface ocean must be used cautiously in highly dynamic environments such as those in the Alboran Sea.  相似文献   

Impact of the Mediterranean Outflow Water on particle dynamics in intermediate waters of the Northeast Atlantic, as revealed by Th and Th     

Sabine Schmidt   《Marine Chemistry》2006,100(3-4):289

Over the last decade ²³⁴Th has become increasingly used to study particle transport in the ocean on a timescale of weeks. The application of ²³⁴Th is mainly focused on the determination of particle and associated carbon fluxes from oceanic surface water. However, ²³⁴Th is also suitable for investigating particle dynamic from the upper ocean down to interface sediments, as illustrated by the present work which reports unexpected behavior of ²³⁴Th in intermediate waters associated with the Mediterranean Outflow Water (MOW). Concentration profiles of dissolved ²³⁸U and ²²⁸Ra, and dissolved and particulate ²³⁴Th and ²²⁸Th were measured in the Mediterranean Outflow Water (MOW) near the Gibraltar Straits and at two sites (36°30′N–15°35′W, Nicole; 36°27′N–10°35′W, Yseult) which had hydrographic characteristics of Meddies, i.e. MOW that propagates as eddies in the Northeastern Atlantic at intermediate depths.There are marked differences in the distribution of thorium between MOW and the surrounding Atlantic waters. At the youngest Meddy Nicole salinity maximum at 1000 m depth, ²³⁴Th(total) : ²³⁸U and ²²⁸Th(total) : ²²⁸Ra activity ratios are significantly lower than radioactive equilibrium, indicating an unusual deficit of short half-life thorium nuclides. This implies an export of thorium, presumably on particles, from intermediate Meddy Nicole waters. This process is supported by an increase of particulate thorium fluxes measured in sediment traps deployed for two weeks above and within Meddy Nicole. In contrast, offshore Meddy Yseult has more typical profiles of both thorium nuclides that are nearly in equilibrium with their parents. These results indicate that at intermediate depths, the presence of MOW affects the exchange of reactive elements between particles and dissolved forms and enhances the downward flux of particles from intermediate waters in the Northeast Atlantic.  相似文献   

Analytical Electron-Microscopy Fractionation of Fine and Colloidal Particulate-Phosphorus in Riverbed and Suspended Sediments   总被引：4，自引：0，他引：4  

Jérôme Poulenard  Jean-Marcel Dorioz  Françoise Elsass 《Aquatic Geochemistry》2008,14(3):193-210

The impact particulate-phosphorus (particulate-P) has on eutrophication of aquatic systems that greatly depends on its composition. As a result, analysis methods for evaluating particulate-P speciation must be capable of identifying and/or quantifying the wide range of forms particulate-P can take. In the present study, we compare the particulate P speciation of the fine and colloidal fractions of riverbed sediment and suspended matter from two rivers in the Lake Geneva basin (French Alps) as determined with chemical extractions to results of a combined Transmission Electron Microscopy and Energy Dispersive Detection (TEM–EDS) analysis of the same samples. TEM–EDS provides semi-quantitative information about the distribution of P throughout the solid fraction of a sample and on the diversity of carrier phases, which are identified by their morphology and stochiometry. EDS-detectable quantities of phosphorus were found in 15–35% of the particles in the samples analyzed. As expected, particulate-P existed in a wide variety of forms, mostly associated with Al, Fe, Ca and Si. Some types of particles, often well-crystallized phosphate minerals, had high P contents (10–30%), but the dominant carrier phases of P were diffuse matrices of particles with low P contents (<5%). These matrices had a wide range of chemical compositions and included clay minerals, crystallized and amorphous phases of Fe, as well as intermediary components. Classical chemical extractions showed major differences in P content and speciation between the upstream and downstream sediment samples. The downstream samples showed higher frequencies of particles containing P, a larger diversity of carrier phases, a higher contribution of clays as carrier phases of P, and the presence of a new fraction with Al and Fe amorphous minerals. The processes that create and select carrier phases of particulate-P are part of the general dynamics of P within a watershed.  相似文献   

獐子岛养殖海域颗粒有机碳、颗粒氮的时空分布特征   总被引：1，自引：1，他引：0  

刘毅  张继红  杜美荣  蔺凡  丁刚  吴文广  房景辉 《海洋科学》2016,40(5):9-18

2011年8月、10月、12月和2012年4月对大连獐子岛养殖海域共14个站位进行了大面调查。对其中颗粒有机碳(POC)和颗粒氮(PN)的时空分布特征进行了研究。结果表明,獐子岛养殖海域水体中POC质量浓度的季节变化趋势是:夏季秋季春季冬季。夏季POC质量浓度最高,表、底层的质量浓度分别为0.159~1.672 mg/L和0.045~0.834 mg/L,平均值分别为(0.867±0.451)mg/L和(0.319±0.204)mg/L。冬季表、底层POC质量浓度最低,表、底层POC质量浓度分别为0.020~0.530 mg/L和0.061~0.458 mg/L。平均值分别为(0.240±0.125)mg/L和(0.221±0.129)mg/L。四个季节的POC质量浓度平面分布较为均匀。PN质量浓度的季节变化趋势是:夏季秋季冬季春季。夏季PN的质量浓度最高,表、底层PN的质量浓度分别为0.026~0.439 mg/L和0.020~0.393 mg/L,平均值分别为(0.193±0.067)mg/L和(0.172±0.060)mg/L。春季表、底层PN质量浓度最低,表、底层PN质量浓度分别为0.059~0.178 mg/L和0.024~0.212 mg/L,平均值分别为(0.120±0.047)mg/L和(0.100±0.050)mg/L。PN与POC的分布特征相似,空间分布均匀。叶绿素a(Chl-a)质量浓度的变化趋势为:夏季秋季春季冬季。POC、PN和Chl-a的垂直分布规律相似,春季底层质量浓度高于表层,夏秋两季表层质量浓度高于底层,冬季表、底层质量浓度基本一致。根据C/N以及POC/Chl-a的比值对POC的来源进行初步分析,表明该海域的POC主要来源于海洋生物,并且受陆源的影响较小。  相似文献   

Reed litter Si content affects microbial community structure and the lipid composition of an invertebrate shredder during aquatic decomposition     

《Limnologica》2016

The decomposition of plant litter is an important mechanism in regard to energy and nutrient dynamics of ecosystems. Silicon concentration of plant tissue can affect these processes by changing litter quality, i.e. nutrient stoichiometry and cellulose and phenols content. To determine which group of microbial decomposers benefits from high Si content in plants and how this impacts on animal decomposers, a batch experiment was conducted with reed leaf litter (Phragmites australis) differing in Si content in the presence/absence of invertebrate shredders (Gammarus pulex). Lipid concentration of G. pulex, in reed litter and fine particulate matter (FPOM) were examined. High Si concentration in reed resulted in a decline of gram positive bacteria in the heterotrophic biofilm and of gram negative bacteria in FPOM. The lipid composition in the next trophic level, the decomposer G. pulex, changed too, indicating a diet shift in favor of bacteria and algae with increasing litter Si concentration. Thus, basal decomposers were affected by the Si availability in plant resources, and these effects likely persist along the food chain, as FPOM is a dominant food supply for other groups, e.g. collectors. This impact of Si content on plant substrate quality for decomposer food webs may have global relevance, due to related modifications in carbon and nutrient cycling during litter decomposition.  相似文献