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1.
太平洋东部CC48孔沉积物稀土元素地球化学研究   总被引:10,自引:0,他引:10  
研究样品于1988年采自太平洋东部CC48孔。通过对沉积物稀土元素地球化学特征的分析发现:(1)各种类型深海沉积物的稀土含量有所差别,以稀土元素总量而论,深海粘土>硅质软泥>硅钙质软泥>钙质软泥;沉积物中的自生矿物、硅质生物成因的非晶质SiO2及碎屑矿物对稀土元素起富集作用,而生物CaCO3则起分散作用。(2)稀土元素含量随深度发生变化。为地层划分提供了依据,应用元素地层学方法将岩芯分成5个层段。  相似文献   

2.
We analyzed the REE, Mn and Al concentrations and Nd isotopic ratios in marine suspensions collected on filters (0.65 μm porosity) with in situ pumping systems in the tropical northeastern Atlantic (20°N, 18–31°W). Previously we reported the same parameters on large sinking particles collected with moored sediment traps at the sites. Shale-normalized REE patterns of the filtered suspensions are characterized by a larger light REE (LREE) to heavy REE (HREE) enrichment compared to the trapped material and a Ce anomaly that evolves positively with depth. Depth profiles of REE/Al show maximum values at 50–100 m, where the Mn/Al ratio also reaches a maximum. The profile of the Nd isotopic ratios of the filtered suspensions shows variations similar to those of the seawater. These results suggest that the filtered suspensions preferentially scavenge the LREE, especially Ce, and that the particulate Mn oxides are potential REE carriers. The relationship between the Ce anomaly and the Ce/Al ratio demonstrates that the particulate Ce anomaly is formed by (1) the LREE adsorption onto the particulate Mn oxides in the surface water, (2) Ce(III) oxidation to insoluble Ce(IV)O2 and (3) preferential desorption of strict trivalent REE from the Mn oxides in deep water. Estimated authigenic Nd contents, using Nd isotopic ratios, decrease with depth. This is consistent with the adsorption of the REE in surface water and their desorption in deep water, suggested by the Ce anomaly formation. All the results show that the suspended particles record more clearly the authigenic REE contribution than the trapped material does. The suspended matter plays a key role in the scavenging of particle-reactive elements.  相似文献   

3.
Guest editorial     
Surficial sediments rich in apatite pellets were recovered from an 80‐m‐deep area that runs parallel to the eastern coast of Vizcaino Bay, Baja California. This area is subject to intense seasonal upwelling, the sediments presenting elevated phosphate (P2O5), organic carbon (Corg), and carbonate concentrations. The pellets are moderately well sorted, concentrated mainly in the 3ø size class within a poorly sorted sediment matrix. Abundant nodular apatite and phosphatized bone fragments were found in only one of the pellet‐bearing samples. This sample has a P2O5concentration of over 20%, the ≥ — 2.5ø to 0.5ø grain size classes alone being formed of up to 32% P2O5. The high proportion of fragmented nodules and the presence of volcanic rock pebbles indicate that at least part of this deposit is allochthonous. The apatite pellets have a flat to concave‐downward heavy rare earth (HREE) shale normalized pattern and, except for La, are depleted in light rare earth elements (LREE). The close resemblance between the HREE patterns and the relatively high La concentration in the pellets of Vizcaino Bay, and the onland phosphorites of the southern Baja California Peninsula, suggest similar depositional histories for these deposits. No significant Ce anomalies were observed, but a negative Eu deviation is common in all of the pellet‐bearing sediments. The depletion of LREE in the pellets of Vizcaino Bay may indicate the preferential removal of these elements by weathering processes.  相似文献   

4.
Six manganese crusts, 13 manganese nodules, and 16 sediments were analyzed by instrumental neutron activation analysis. Data were generated on selected major and minor elements but geochemical evaluations are based only on Fe, Sc, U, Th, and the rare earth elements (REE). Manganese crusts and manganese nodules have comparable trivalent REE contents and show a shale‐like distribution pattern. Both crusts and nodules are characterized by a positive Ce anomaly but the anomaly is higher in nodules. REE contents in manganese nodules show a linear dependence on the Fe content, and it is concluded that these elements are incorporated in the Fe‐rich (δ‐MnO2) phase. In the crusts, the REE correlate with Sc and are therefore assumed to be associated with the clay minerals. Uranium contents are significantly higher in the crusts than in nodules whereas Th is slightly higher in the nodules. There is a clear positive correlation between U and Th in nodules but there are too few data to make a similar conclusion for crusts. Compositional data suggest a division of the sediments into two groups. The carbonate sediments have much lower REE contents and a more pronounced negative Ce anomaly than the clays, while both show a lithogenous component as indicated by a slight negative Eu anomaly.  相似文献   

5.
Detailed lithological, biogeochemical and molecular biological analyses of core sediments collected in 2002–2006 from the vicinity of the Malenky mud volcano, Lake Baikal, reveal considerable spatial variations in pore water chemical composition, with total concentrations of dissolved salts varying from 0.1 to 1.8‰. Values of methane δ13С in the sediments suggest a biogenic origin (δ13Сmin. ?61.3‰, δ13Сmax. ?72.9‰). Rates of sulphate reduction varied from 0.001 to 0.7 nmol cm?3 day?1, of autotrophic methanogenesis from 0.01 to 2.98 nmol CH4 cm?3 day?1, and of anaerobic oxidation of methane from 0 to 12.3 nmol cm?3 day?1. These results indicate that methanogenic processes dominate in gas hydrate-bearing sediments of Lake Baikal. Based on clone libraries of 16S rRNA genes amplified with Bacteria- and Archaea-specific primers, investigation of microbial diversity in gas hydrate-bearing sediments revealed bacterial 16S rRNA clones classified as Deltaproteobacteria, Gammaproteobacteria, Chloroflexi and OP11. Archaeal clone sequences are related to the Crenarchaeota and Euryarchaeota. Baikal sequences of Archaea form a distinct cluster occupying an intermediate position between the marine groups ANME-2 and ANME-3 of anaerobic methanotrophs.  相似文献   

6.
Abstract

Chemical parameters (pH, Eh, carbon, Kjeldahl nitrogen, total phosphorus, 0.5M H2SO4‐extractable phosphorus, organic phosphorus, and water‐soluble phosphorus) were measured in the surface layers of sediments collected from various depths in Lakes Rotowhero, Okaro, Ngapouri, Rotokakahi, Okareka, Tikitapu, Okataina, and. Rotoma during October 1972. The sediments of the productive geothermal lake, Rotowhero, were markedly different from those of the cold‐water lakes: they had relatively low pH values, high carbon (mean 8.5%) and organic phosphorus (mean 4160 μg.g?1) concentrations, and very high total phosphorus concentrations (mean 4770 μg.g?1), probably as a result of enrichment by hot springs.

The mean concentrations in the sediments of the cold‐water lakes were carbon 3.2–7.9%, Kjeldahl nitrogen 3380–8310 μg.g?1 and phosphorus 690–1780 μg.g?1. These concentrations are within the ranges for New Zealand terrestrial topsoils, but the lake sediments appear enriched in phosphorus relative to local topsoils. Total carbon, nitrogen, and phosphorus concentrations of sediments tended to be highest in the eutrophic lakes (Okaro, Ngapouri) although the deep oligotrophic lakes (Okataina, Rotoma) had relatively high total phosphorus concentrations (means 1400, 1510 μg.g?1). Overall, the carbon, nitrogen, and phosphorus concentrations of the sediments showed little relationship to the trophic state of the lake.

Organic phosphorus concentrations of the surface layers of sediments were similar in all the cold‐water lakes (mean 319 μg.g?1). The proportion of the total phosphorus apparently ‘fixed’ in mineral material was minimal (0–1%) in sediments from the eutrophic and mesotrophic lakes, but in the oligotrophic lakes was similar to that in New Zealand topsoils (9–14%). Reducing conditions may cause solution of a high proportion of the ‘fixed’ phosphorus in the eutrophic lakes.

The water‐soluble phosphorus concentrations in the sediments of the five shallow cold‐water lakes (Okaro, Ngapouri, Rotokakahi, Okareka, Tikitapu) correlated positively with trophic state and with concentrations of dissolved phosphorus in the lake waters.

Carbon, nitrogen, and phosphorus concentrations in the sediments tended to vary with overlying water depth. This should be considered when comparisons are made between lakes.  相似文献   

7.
The circulation of methane-rich fluids at cold seeps often leads to the precipitation of seep carbonates close to the seafloor along continental margins, which can be used as records of past fluid seepage. Rare earth element (REE) concentrations in seep carbonates have been used to trace fluid sources and provide information on associated biogeochemical processes at cold seeps. The REE concentrations of a series of carbonates collected from cold seeps in the southwestern Dongsha area of the northern South China Sea are analyzed in this study. The total REE contents (ΣREE) of the seep carbonates analyzed show a wide variation from 17 ppm to 523 ppm with an average ΣREE value of 54 ppm, which are higher than the typical marine carbonate values of ∼28 ppm commonly reported and also higher than those of the carbonates from other cold seep areas. A positive correlation between Fe–Mn content and ΣREE was observed. These results suggest that the seep carbonates of this study were primarily controlled by the methane-derived fluid from which they precipitated. The Fe-rich dolomite and siderite, which are the main components of the carbonates, are responsible for the enrichment of the REE. A slight positive Ce anomaly observed in the shale-normalized REE patterns of the studied seep carbonates suggests that they formed in anoxic conditions, and the correlations between Ce/Ce* and LaN/SmN, Ce/Ce* and DyN/SmN, Ce/Ce* and ΣREE further reveal that the REE characteristics of most seep carbonate samples preserve the original redox conditions in which they precipitated and late diagenesis has had little effect on the REE. However, the REE characteristics of sub-samples DS2-2B, DS1-6A and DS1-7A are very different from those of the other sub-samples, indicating a greater impact of late diagenesis and post-oxidation favored REE enrichment.  相似文献   

8.
In conventional studies of tracing dolomitization and diagenetic fluids, REEs of dolomites were widely used as been normalized by PAAS, NASC or chondrite. However, most dolomites are formed in seawater or seawater-derived fluids. Thus, we conduct a new attempt to normalize the REEs of dolomite using seawater standard, based on case studies on 36 Triassic limestone–dolomite samples from the Geshan section of southeast China and 26 Permian–Triassic dolomite samples from the Panlongdong section of northeastern Sichuan Basin, southwest China.The Geshan seawater-normalized (SN) REE patterns are characterized by notable positive CeSN (average CeSN/Ce* = 6.823, SD = 0.192) and negative PrSN anomalies (average PrSN/Pr* = 0.310, SD = 0.010), and slightly negative GdSN anomalis (average GdSN/Gd* = 0.864, SD = 0.053), with no obvious EuSN anomaly (average EuSN/Eu* = 1.036, SD = 0.094). The signatures of REE patterns barely changed during the dolomitization process. For the REE compositions of the Panlongdong dolomite, it can be found that (1) the recrystallization process can result in varied total REE concentrations (between 7.16 ppm and 37.87 ppm), but do not alter the REE patterns, including consistent positive CeSN anomalies (average = 4.074, SD = 0.27) and LREE enrichment (average NdSN/YbSN = 3.164, SD = 0.787); (2) meteoric incursion can reverse Ce anomaly, from the strong positive Ce anomalies (CeSN/Ce* = 5.059) to slightly positive (CeSN/Ce* = 2.459) or even negative Ce anomalies; and (3) hydrothermal fluid altered REE pattern is complicated by fluctuated distribution curve, negative Ce anomaly and positive Eu anomaly (EuSN/Eu* = 1.862). These results suggest that the seawater normalized REE patterns of dolomite can serve as an index to study the source of the dolomitization fluids and distinguish complex diagenetic processes, providing a complement to previous works.  相似文献   

9.
Rare earth elements (REEs) of 91 fine-grained bottom sediment samples from five major rivers in Korea (the Han, Keum, and Yeongsan) and China (the Changjiang and Huanghe) were studied to investigate their potential as source indicator for Yellow Sea shelf sediments, this being the first synthetic report on REE trends for bottom sediments of these rivers. The results show distinct differences in REE contents and their upper continental crust (UCC)-normalized patterns: compared to heavy rare earth elements (HREEs), light rare earth elements (LREEs) are highly enriched in Korean river sediments, in contrast to Chinese river sediments that have a characteristic positive Eu anomaly. This phenomenon is observed also in primary source rocks within the river catchments. This suggests that source rock composition is the primary control on the REE signatures of these river sediments, due largely to variations in the levels of chlorite and monazite, which are more abundant in Korean bottom river sediments. Systematic variations in ΣLREE/ΣHREE ratios, and in (La/Yb)–(Gd/Yb)UCC but also (La/Lu)–(La/Y)UCC and (La/Y)–(Gd/Lu)UCC relations have the greatest discriminatory power. These findings are consistent with, but considerably expand on the limited datasets available to date for suspended sediments. Evidently, the REE fingerprints of these river sediments can serve as a useful diagnostic tool for tracing the provenance of sediments in the Yellow Sea, and for reconstructing their dispersal patterns and the circulation system of the modern shelf, as well as the paleoenvironmental record of this and adjoining marginal seas.  相似文献   

10.
The aim of this study was to evaluate the erodibility of submarine coastal sediments for the purpose of modelling sediment dynamics in Mecklenburg Bay, south-western Baltic Sea. Erosion thresholds derived from experiments with a device microcosm on cores of fine sand (n=5, mean grain size=132 µm) and mud (n=5, medium silt size, mean=21 µm), collected at different times of the year, were compared to theoretical critical shear stress velocities based on grain-size measurements. For this purpose, a sedimentological map of natural surface sediments was constructed for the study area. Calculated values for critical shear stress velocities (u* cr-Hjulström ) are 1.2 cm s?1 for fine sand, and 3.75 cm s?1 for cohesive mud. At the mud station, erosion experiments showed an initial transport of the fluffy surface layer (u* cr-initial ) at a mean critical shear stress velocity of 0.39 cm s?1. Initial rolling transport at the fine sand station for single sand grains was recorded at values of 0.5 cm s?1. At higher shear stress velocities, the two sediment types showed diverging erosion behaviour. Measurable erosion (ε>5.0×10?6 kg m?2 s?1) of fine sand starts at a mean critical shear stress velocity (u* cr-erosion ) of 1.15 cm s?1 whereas fluffy surface material on mud cores was eroded at mean u* cr-erosion of 0.62 cm s?1. This indicates that measured erosion thresholds at the fine sand site fit well to calculated critical shear stress velocities whereas calculated erosion thresholds for cohesive mud are roughly 6 times higher than measured values. As erosion behaviour at the mud station was dominated by fluffy surface material, the comparability of measured and calculated threshold values may be reduced. The underlying silt-sized sediment itself was stable due to cohesive effects. This behaviour has to be taken into consideration by using sediment types instead of mean grain sizes for mapping and modelling sediment dynamics. A comparison of the near-bottom hydrodynamic conditions in the study area and experimentally derived critical shear stress velocities suggests that particle transport is controlled by storm events whereas under calm conditions shear stress velocities do not exceed the critical values.  相似文献   

11.
Chemical extraction techniques show that the majority of the arsenic in North Atlantic deep-sea sediments is associated with an iron phase compositionally similar to that found in deep-sea ferromanganese nodules (As/Fe ~ 11 · 10?4) and is probably of seawater origin. Some sediments also contain As associated with Fe oxides produced by continental weathering. A minority (~8%) of the arsenic is of detrital origin but is not associated with Fe or Mn oxides; it has a content (1.7 ppm) similar to the average crustal abundance. In the Eastern Mediterranean Sea, near-shore sediments contain As associated with land-derived Fe oxides (As/Fe ~ 2 · 10?4), but As/Fe ratios increase to ~ 13 · 10?4 in deep-sea sediments as the contribution of seawater derived arsenic becomes dominant. Arsenic is enriched in metalliferous sediments (As/Fe ~ 20?50 · 10?4) but As/P ratios of metalliferous sediments, deep-sea ferromanganese nodules and deep-ocean water are all similar. Although a hydrothermal contribution cannot be discounted, it is likely that the arsenic is also of seawater origin, suggesting that hydrothermal iron oxyhydroxides remove As more efficiently from seawater than do iron phases (goethite) in deep-sea sediments and nodules. Arsenic accumulates in deep-sea sediments (~ 6 μg cm?2 10?3 yr?1) at sediments (~ 120 μg cm?2 10?3 yr?1) at rate sufficient to balance river input input (~3 · 1010 g yr?1). These estimates give an oceanic residence time for arsenic of 1–2 · 105 yr.  相似文献   

12.
Concentrations of dissolved methane in seawater and bottom sediments, as well as of methane emanating from gas seeps were measured at 18 stations including several small bays in the Sevastopol coastal area (Black Sea) during 2007–2008. Methane concentrations in surface waters ranged from 10 to 2,970 nmol l?1, and correlated well with values recorded for sediments. Methane concentrations in the water column were influenced by water depth, as well as by air and water temperatures. In the spring and summer of 2008, in situ CH4 saturation relative to air was in the range of 970–71,900%. Maximum saturation was in summer. CH4 fluxes to the atmosphere from the Sevastopol coastal area were estimated to vary from 190 to 1,550 μmol m?2 day?1. Gas bubbles escaping from the seepages contained about 57 vol% methane. Radiocarbon dating of the methane revealed an age not exceeding 150 years, implying a biogenic origin.  相似文献   

13.
Anaerobic salt marsh sediments were amended with a variety of organic pollutants and the effects on methanogenesis, sulfate reduction and carbon dioxide evolution were examined. Addition of 1000 μg g?1 (dry weight sediment) Arochlor 1221, lindane, endrin, benzene and phenanthrene resulted in no significant effects on the activities studied. Methanogenesis was inhibited by 1000 μg g?1toxaphene, PCP, chlordane, naphthalene, DDT, Kepone and heptachlor and by 100 μg g?1 PCP and toxaphene. At 1000 μg g?1 naphthalene and toxaphene and 100 μg g?1 PCP, a period of initial inhibition of methanogenesis was followed by stimulation relative to controls. Arochlor 1254 (1000 μg g?1) and Temik (500 and 10 μg g?1) stimulated methanogenesis from the outset. Temik at 500 μg g?1 gave the greatest stimulation of methanogenesis (900% of controls) of any of the compounds studied. Sulfate reduction was inhibited by 1000 μg g?1 PCP, toxaphene, naphthalene and chlordane and by 500 μg g?1 atrazine and 100 μg g?1 heptachlor. Sustained inhibition of sulfate reduction by naphthalene, toxaphene and PCP may have contributed to the stimulation of methanogenesis. Carbon dioxide evolution was not significantly affected by most of the compounds studied except for 100 μg g?1 PCP and 1000 μg g?1 aphthalene, each of which gave significant inhibition in only one of three experiments.Concentrations of individual organic pollutants required to cause observable effects were high. It is concluded that, except for highly polluted sediments, methanogenesis, sulfate reduction and CO2 evolution would not be affected by the compounds studied here at concentrations typically found in the environment.  相似文献   

14.
The different mineral phases of the ferromanganese (Fe–Mn) crusts stem from the interaction of biotic and abiotic components. It is therefore vital to study the activity of these components to decipher their contribution to the enrichment/depletion of metals in the crust. Thus, the present study examined sorption and release of Co and Ni by Fe-Mn crusts with associated microbial communities in the presence and absence of the metabolic poison sodium azide (15?mM). The study was conducted in the presence (G+) and absence (G?) of added glucose (0.1%) at temperatures of 4?±?1°C and 28?±?2°C. Results showed that the microbial community had maximal sorption of Co of 66.12?µg?g?1 at 4?±?1°C in the absence of added glucose and 479.75?µg?g?1 at 28?±?2°C in the presence of added glucose. Maximum sorption of Ni in the absence of added glucose was 1.89?µg?g?1 at 4?±?1°C and release of Ni was 51.28?µg?g?1 in the presence of added glucose. Under abiotic conditions with 15?mM sodium azide as a metabolic inhibitor, significant amounts of Co and Ni were released in the G+ medium. Total cell counts on the Fe-Mn crust in the presence of added glucose increased by an order of magnitude from 106 to 107 cells g?1 and in the absence of added glucose remained within the order of 106 cells?g?1 irrespective of temperature of incubation. Microscopic observation of the samples from biotic incubations showed numerous bacterial cells, exopolysaccharides, and structures resembling secondary minerals formed by bacteria. The results indicate that bacteria promote the enrichment of Co and Ni on the hydrogenetic Fe-Mn crusts by sorption processes and release of Ni by reductive dissolution of the oxides. The higher enrichment of Co than Ni is attributed to the way in which microbes interact with the metals.  相似文献   

15.
Authigenic carbonates are common at cold seep sites as a result of microbial oxidation of hydrocarbons. Seep carbonate samples were collected from the surface of the Bush Hill (Green Canyon Block 185, Gulf of Mexico), a mound containing gas hydrate. The carbonates consisted of oily, porous limestone slabs and blocks containing bioclasts and matrix. Analysis by X-ray diffraction shows that aragonite is the dominant mineral (89–99 wt% with an average of 94 wt%) in the matrix of seep carbonate. This cement occurs in microcrystalline, microspar, and sparite forms. The moderate 13C depletion of the seep carbonate (the most depleted one has δ13C value of −29.4‰, and 26 of 38 subsamples have δ13C values >−20.0‰) indicates that the non-methane hydrocarbons was incorporated during seep carbonate precipitation. Relative enrichment of 18O may be related to localized destabilization of gas hydrate or derived from 18O-enriched pore water originated from smectite–illite transition in the deep sediments. The total content of rare earth elements (REE) of the 5% HNO3-treated solution of the carbonates is from 0.40 ppm to 30.9 ppm. The shale-normalized REE patterns show varied Ce anomalies from significantly negative, slightly negative, and no to positive Ce anomalies. Variable content of trace elements, total REE, and Ce anomalies in different samples and even in the different carbonate mineral forms (microcrystalline, microspar and sparite) of the same sample suggest that the formation condition of the Bush Hill seep carbonate is variable and complex, which is possibly controlled by the rate of fluid flux.  相似文献   

16.
北冰洋深海广泛分布的富锰棕色沉积层(棕色层)是海冰、洋流、物源供给等多种因素共同作用的结果,本文基于西北冰洋门捷列夫海岭ARC07-E25岩芯沉积物稀土元素与微量元素含量、颜色反射率参数、粗颗粒组分和无机碳含量的变化特征,对该类沉积层中稀土元素的组成特征、形成机制和物质来源进行了综合分析。结果显示,沉积物稀土元素总含量(∑REE)在122.37×10?6~231.94×10?6之间变化,北美页岩标准化配分模式显示出轻微的中稀土(MREE)富集以及由La、Ce、Nd主导的较强的轻稀土(LREE)优势。沉积物中∑REE随着粗组分颗粒(如冰筏碎屑)的增多而呈现降低趋势,表明门捷列夫海脊沉积物中的稀土元素主要富集在细粒沉积物中。根据∑REE在沉积物中的变化特征将E25岩芯沉积物划分为4种地层,反映出了冰期/间冰期的气候转变过程中温暖条件下形成的棕色层与寒冷条件下形成的浅灰绿色沉积层(灰色层)的岩性旋回中稀土元素组成的差异,由于两种沉积层在形成时受到不同的底层水氧化还原环境的控制,导致了铈(Ce)元素在氧化水体中会由Ce3+氧化为Ce4+并发生沉降,而在还原水体中则由Ce4+还原为Ce3+发生溶解,这一特性使LREE含量产生较大波动,进而影响到∑REE,使之趋于在代表氧化条件的棕色层中升高而在代表还原条件的灰色层中降低。R型因子分析和物质来源判别结果显示,E25岩芯沉积物中稀土元素与亲碎屑元素(Nb、U、Th)有较好的相关性,主要来源于东西伯利亚海和新西伯利亚群岛的近岸侵蚀物质以及勒拿河物质的输入。  相似文献   

17.
Myanmar is tenth among the world’s fish-producing countries and third in ASEAN (Association of Southeast Asian Nations). To understand the mechanisms underlying the high production, oceanographic and phytoplankton surveys, including primary productivity measurements based on pulse amplitude modulation fluorometry, were conducted near an active fishing ground near Myeik City. Three surveys, one in each of the representative seasons and covering the characteristic coastal environments, showed well-defined seasonality in primary production and phytoplankton occurrence. End of the dry season was the most productive, with productivity of 2.59 ± 1.56 g C m?2 day?1 and high concentration of chlorophyll a (3.14 ± 2.64 µg L?1). In this season, the phytoplankton population was dominated by high densities of the diatoms Bellerochea horologicalis and Chaetoceros curvisetus, whereas primary productivity was low at the onset of the dry season, 1.36 ± 0.77 g C m?2 day?1. However, this low primary production might be compensated by activation of microbial food chains originating from high dissolved organic carbon. The rainy season exhibited the lowest production, 6.6% of the end of the dry season, due to the extensive discharge of turbid water from the rivers which lowered euphotic layer depth and resulted in an unusually high diffuse attenuation coefficient of 2.30 ± 1.03 m?1. This incident of turbid water may be related to soil erosion from deforestation and mangrove deterioration. This research reveals the seasonal trend in Myanmar’s coastal productivity and its relationship to the tropical monsoon climate as well as emphasizing the importance of tropical coastal environments to the sustainability of the fisheries.  相似文献   

18.
We investigated the water-column light utilization efficiency (Ψ) of phytoplankton photosynthesis in the Western Subarctic Gyre (WSG) of the North Pacific during summer 2008. The Ψ values (0.64–1.86 g C [g Chl a]?1 [mol photon]?1 m2) obtained were observed to increase significantly with decreasing daily photosynthetic available radiation (PAR) and were generally higher than those of previous studies, not only from the subarctic Pacific but also from the world’s oceans. To examine the effect of iron availability on Ψ in the WSG, Ψ values were estimated from the data of two in situ iron fertilization experiments: the Subarctic Pacific Iron Experiment for Ecosystem Dynamics Study I (SEEDS-I) and II (SEEDS-II). We found that iron availability did not affect Ψ values. Overall, this study revealed that Ψ values changed remarkably in the WSG during the summer, and that higher values were found at the stations where moderate PAR levels (ca. 10–30 mol photons m?2 day?1) were observed and where autotrophic flagellates predominated in the phytoplankton assemblages.  相似文献   

19.
Ferromanganese nodules and crusts contain relatively high concentration of rare earth elements(REE) and yttrium(REY),with a growing interest in exploitation as an alternative to land-based REY resources.On the basis of comprehensive geochemical approach,the abundance and distribution of REY in the ferromanganese nodules from the South China Sea are analyzed.The results indicate that the REY contents in ferromanganese deposits show a clear geographic regularity.Total REY contents range from 69.1×10~(–6) to 2 919.4×10~(–6),with an average value of 1 459.5×10~(–6).Especially,the enrichment rate of Ce content is high,accounting for almost 60% of the total REY.This REE enrichment is controlled mainly by the sorption of ferromanganese oxides and clay minerals in the nodules and crusts.Moreover,the total REY are higher in ferromanganese deposits of hydrogenous origin than of diagenetic origin.Finally,Light REE(LREE) and heavy REE(HREE) oxides of the ferromanganese deposits in the study area can be classified into four grades: non-enriched type,weakly enriched type,enriched type,and extremely enriched type.According to the classification criteria of rare earth resources,the Xisha and Zhongsha platform-central deep basin areas show a great potential for these rare earth metals.  相似文献   

20.
Rates of respiration and ammonia excretion of Euphausia hanseni and Nematoscelis megalops were determined experimentally at four temperatures representative of conditions encountered by these euphausiid species in the northern Benguela upwelling environment. The respiration rate increased from 7.7 µmol O2 h?1 gww ?1 at 5 °C to 18.1 µmol O2 h?1 gww ?1 at 20 °C in E. hanseni and from 7.0 µmol O2 h?1 gww ?1 (5 °C) to 23.4 µmol O2 h?1 gww ?1 (20 °C) in N. megalops. The impact of temperature on oxygen uptake of the two species differed significantly. Nematoscelis megalops showed thermal adaptations to temperatures between 5 °C and 10 °C (Q10 = 1.9) and metabolic constraint was evident at higher temperatures (Q10 = 2.6). In contrast, E. hanseni showed adaptations to temperatures of 10–20 °C (Q10 = 1.5) and experienced metabolic depression below 10 °C (Q10 = 2.6). Proteins were predominantly metabolised by E. hanseni in contrast to lipids by N. megalops. Carbon demand of N. megalops between 5 and 15 °C was lower than in E. hanseni versus equal food requirements at 20 °C. It is concluded that the two species display different physiological adaptations, based on their respective temperature adaptations, which are mirrored in their differential vertical positioning in the water column.  相似文献   

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