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海水中胶体有机碳研究简介 总被引：3，自引：0，他引：3
随着海洋碳通量研究的深入和切向超滤技术的完善,对海洋中胶体有机碳的研究引起越来越广泛的重视,本文介绍了近年来海洋中胶体有机碳研究的发展状况。１胶体有机碳的定义及其研究意义１．１定义海水中的有机碳以溶解有机碳（ＤＯＣ）、颗粒有机碳（ＰＯＣ）和挥发有机碳（ＶＯＣ）３种形式存在［１］。其中,ＤＯＣ和ＰＯＣ之间的区分,在操作上是以能否通过０．４５μｍ孔径的滤膜为标准。近年来,随着对胶体粒子研究的发展,这一标准已不能满足对有机碳分类的要求［３］。水环境中的胶体,被定义为１ｎｍ到１μｍ范围内的粒子,而在分离… 相似文献
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东地中海沉积后氧化作用造成的腐泥的改造和清除Ｎ．Ｃ．Ｈｉｇｇｓ等厚度大于１ｃｍ、有机碳含量大于２％的沉积层叫腐泥。大部分深水沉积中有机碳含量低，因此腐泥的形成需要特定的海洋地理条件。然而，在近４００ｋａ中，东地中海发育有至少１２层这样的腐泥，它们具有... 相似文献
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宁波及其邻近海域沉积物释放耗氧有机物（COD）的初步研究 总被引：2，自引：0，他引：2
本文通过对城市污水纳污海区沉积物样品释放有机物的研究，初步揭示了沉积物释放耗氧有机物（ＣＯＤ）的一般规律。研究表明宁波海域沉积物释放ＣＯＤ的范围在０．１５×１０－３～０．８０×１０－３之间，释放速率平均为１０３．９ｍｇ／（ｍ２．ｄ）；舟山沈家门附近海域沉积物释放ＣＯＤ速率平均为２５３．１ｍｇ（ｍ２·ｄ）。沉积物释放ＣＯＤ的量与沉积物中有机质的含量成正比，而其释放速率与沉积物有机质的含量关系不大。 相似文献
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鸭绿江口溶解有机碳的研究 总被引：3，自引：2，他引：1
１９９６年５月采样测定鸭绿江口溶解有机碳（ＤＯＣ）的含量,得出分布变化特征,并同其它一些河口的溶解有机碳进行了比较。鸭绿江口表层水溶解有机碳的平均含量为２０８μｍｏｌＣ／Ｌ。在盐度大于１．６的河口区,溶解有机碳的分布主要受海水稀释作用控制;在盐度０～１．６的区域溶解有机碳的浓度随盐度的增加而明显增加。在最大混浊带,ＤＯＣ的浓度最高,表明有颗粒有机碳转化为溶解有机碳。丹东市以上流段,河水中溶解有机碳的含量相对较低,说明由丹东市引入的工业及生活污水对鸭绿江水体中溶解有机碳的含量有一定的影响。 相似文献
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台湾地区湖泊水库悬浮颗粒有机质之碳、氢、氧、氮、硫元素计量分析 总被引：1，自引：0，他引：1
对台湾地区１８个湖泊水库水体中悬浮颗粒有机质之碳，氢，氧，氮，硫和叶绿素α的含量进行了分析，其中ＰＯＯ乃首度以元素分析仪直接测量。结果为，ＰＯＣ，ＰＯＨ，ＰＯＯ，ＰＯＮ，ＰＯＳ含量分别介于１３８－８３７０μｇ／Ｌ，１３．７－９２６．１μｇ／Ｌ，３１－２６２３μｍ／Ｌ，１４－１２６５μｇ／Ｌ，１．９－４９．７μｇ／Ｌ之间，Ｃｈ１．ａ含量则介于０．３１－９６．７５μｇ／Ｌ之间，ＰＯＭ元素间原子数关系为 相似文献
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中国海域及邻区某些盆地生油岩的有机地球化学特征 总被引：1，自引：0，他引：1
蓝先洪 《海洋地质与第四纪地质》1992,(3)
本文根据有机地球化学资料,研究和探讨了中国海域及邻区某些盆地生油岩的有机质丰度、可溶有机质的组成特征和不溶有机质的性质。结果表明,绝大多数生油岩有机碳含量大于0.90％,氯仿沥青“A”含量平均值大于600ppm,总烃大于200ppm。母质类型为腐殖—腐泥型和腐泥—腐殖型。 相似文献
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沉积物插管短柱样品于2013年4月采自大连湾2010年“7·16”溢油事故污染区,BQ050站与BQ007站分别位于生物分散剂和化学分散剂喷洒区。沉积物的可溶有机质含量(沥青A)、有机碳同位素组成(δ13Corg)和210Pb比活度分析结果表明:喷洒生物分散剂的重污染区(BQ050站),沉积物中TOC含量为0.58%～1.51%,平均为1.15%;δ13Corg值为-22.2‰～-20.5‰PDB,平均为-21.74‰PDB;沥青A含量为0.061 5%～0.566 4%,平均为0.174 9%;沥青A/TOC比值为7.0%～34.8%,平均为14.13%;210Pbex比活度存在异常峰值分布,垂向分布特征与沥青A相似;2～16 cm段沉积物的可溶有机质具有明显的外来输入特征。喷洒化学分散剂的较轻污染区(BQ007站),沉积物中TOC含量为0.61%～1.14%,平均为0.87%,除8～14 cm层段外,比BQ050站略低;但沥青A含量与沥青A/TOC比值明显低于前者;δ13Corg值较BQ050站轻;210Pbex比活度随柱样深度呈指数衰减,对数相关;外来有机质输入量较低。截至2013年4月,BQ050站溢油污染物在海底下16 cm深度处有特征信号,溢油污染物沥青A 组分垂向迁移距离约为15 cm。 相似文献
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Rare earth element geochemistry in cold-seep pore waters of Hydrate Ridge, northeast Pacific Ocean 总被引：2，自引：1，他引：1
Tobias Himmler Brian A. Haley Marta E. Torres Gary P. Klinkhammer Gerhard Bohrmann Jörn Peckmann 《Geo-Marine Letters》2013,33(5):369-379
The concentrations of rare earth elements (REEs), sulphate, hydrogen sulphide, total alkalinity, calcium, magnesium and phosphate were measured in shallow (<12 cm below seafloor) pore waters from cold-seep sediments on the northern and southern summits of Hydrate Ridge, offshore Oregon. Downward-decreasing sulphate and coevally increasing sulphide concentrations reveal sulphate reduction as dominant early diagenetic process from ~2 cm depth downwards. A strong increase of total dissolved REE (∑REE) concentrations is evident immediately below the sediment–water interface, which can be related to early diagenetic release of REEs into pore water resulting from the re-mineralization of particulate organic matter. The highest pore water ∑REE concentrations were measured close to the sediment–water interface at ~2 cm depth. Distinct shale-normalized REE patterns point to particulate organic matter and iron oxides as main REE sources in the upper ~2-cm depth interval. In general, the pore waters have shale-normalized patterns reflecting heavy REE (HREE) enrichment, which suggests preferential complexation of HREEs with carbonate ions. Below ~2 cm depth, a downward decrease in ∑REE correlates with a decrease in pore water calcium concentrations. At this depth, the anaerobic oxidation of methane (AOM) coupled to sulphate reduction increases carbonate alkalinity through the production of bicarbonate, which results in the precipitation of carbonate minerals. It seems therefore likely that the REEs and calcium are consumed during vast AOM-induced precipitation of carbonate in shallow Hydrate Ridge sediments. The analysis of pore waters from Hydrate Ridge shed new light on early diagenetic processes at cold seeps, corroborating the great potential of REEs to identify geochemical processes and to constrain environmental conditions. 相似文献
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Diagenetic deposition of manganese in sediment of a historically meromictic lake,Lake Suigetsu,Japan
Vertical profiles of manganese concentration in interstitial waters and of manganese and iron contents in five chemically-separated fractions of sediments have been studied in a sediment core (73 cm long) from a meromictic lake, Lake Suigetsu, which changed from freshwater to brackish conditions in 1664 A.D. The interstitial waters show a minimum manganese concentration of 0.13 ppm near a depth of 10 cm and a maximum of 26 ppm near 65 cm in the core. A predominant amount of manganese, up to 0.17%, is found in the hydrogen peroxide-soluble fraction of sediments in layers above a depth of 52 cm. It is suggested that the manganese is included in stable iron sulfides such as pyrite. Manganese, which diffuses upward from the lower layer, is thought to be deposited along with stable iron sulfide during diagenetic formation of the latter near a depth of 10 cm in the core. 相似文献
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N. H. Khadge 《Marine Georesources & Geotechnology》2000,18(3):251-258
As a part of the environmental impact assessment studies, geotechnical properties of sediments were determined in the Central Indian Basin. The undrained shear strength and index properties of the siliceous sediments were determined on 20 box cores of uniform dimension collected from various locations in five preselected sites. The maximum core length encountered was 41 cm and most of the sediments were siliceous oozes consisting of radiolarian or diatomaceous tests. The shear strength measurements revealed that surface sediments deposited in recent times (0-10 cm) have a shear strength of 0-1 kPa; this value increases with depth, reaching 10 kPa at 40 cm deep. Older sediments have greater strength because of compaction. Water content varies in the wide range of 312-577% and decreases with depth. The clay minerals such as smectite and illite are dominant and show some control over water content. Wet density, specific gravity, and porosity do not indicate any notable variation with depth, thereby indicating a uniform, slow rate of sedimentation. The average porosity of sediments is 90.2%, specific gravity 2.18, and wet bulk density 1.12 g/cm 3 . Sediments exhibit medium to high plasticity characteristics, with the average plasticity index varying between 105% and 136%. Preliminary studies on postdisturbance samples showed an increase in natural water content and a decrease in undrained shear strength of sediments in the top 10- to 15-cm layer. 相似文献
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An examination of split core photographs from the north-central Pacific reveals the presence of three different burrow morphologies. Simple burrows occur throughout the region. Halo burrows are present in water deeper than 4,000 m (3,000 m along the equator) and removed from continental areas. Imbricate burrows are uncommon and have an irregular distribution. Organisms responsible for the burrows are interpreted as surface to near-surface feeders which do not penetrate deeply into the sediments. Thus, the zone of sediment mixing caused by burrowing ranges from 10 to 30 cm and averages 20 cm. 相似文献
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The major and minor element contents in the sediment core H9 from the hydrothermal fields of the Okinawa Trough show a sharp change at the depth of 80 cm. The elements enriched in the upper 80 cm core are those enriched in the hydrothermal deposits and in the surface sediments recovered from the hydrothermal fields in the trough, which indicates the input of hydrothermal materials. Comparing with other hydrothermal sediments from Mid-ocean Ridges or the Lau Basin, the degree of the enrichment of elements iron, copper,cobalt, and nickel is relatively low. However, the enrichment of elements manganese, lead, arsenic, antimony and mercury is remarkable. The average contents of these elements in the upper 80 cm core sediments are three to six times those in the lower section, and 3~12 times those in the surface sediments which are not influenced by hydrothermal activities. Hydrothermal activities have contributed significant manganese, lead, arsenic, antimony and mercury to the sediments, and these elements are distinct indicators for the hydrothermal activity in the Okinawa Trough. The significant enrichment of these elements in Core H9 upward from the depth 80 cm indicates the start or the significant enhancing of the hydrothermal activity in this area at about 5 740 aB.P. The average accumulation rate of manganese during this period is about 40 461 μg/(cm2·ka), which is similar to the hydrothermal sediments in the Lau Basin or the East Pacific Rise. 相似文献
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A new type of rock drill, which has compact size and a simple mechanism and which can be automatically operated in water, was developed. The drill can obtain 75 cm of rock core from a rocky bottom covered by thin sediments at a maximum depth of 300 m.The drill was operated under a current of 1.5 knots in Sagami Bay south of Tokyo and obtained a 40-cm core of volcanic conglomerate of Miocene age from the slope of a small bank at a depth of 130 m. During the operation the vessel was not anchored. 相似文献
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对东太平洋海盆 ４３０ 柱沉积物的组分、古生物、结构构造以及古地磁、铀系等进行研究后, 将沉积物进行分类、命名与分层, 并确定其年代。研究表明, 本柱由下至上的沉积物分别为含沸石粘土、深海粘土、硅质粘土和钙质粘土。该柱中存在 ４ 个沉积间断, 其中在 ３２５ ｃｍ附近层位有一厚约 １０ ｃｍ 的多金属结核层,此界面为中中新世至晚上新世的沉积间断,它在 Ｃ Ｃ区内普遍存在, 持续时间长, 分布范围广。反映此时南极底层流十分强盛, 对东太平洋 Ｃ Ｃ 区的沉积作用和多金属结核形成与发育产生重要的影响。 相似文献
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东海沉积物中微生物标志物GDGTs年代际变化及来源 总被引：2，自引：0，他引：2
甘油双烷基甘油四醚(Glycerol Dialkyl Glycerol Tetraethers,GDGTs)是近几年来新发现的一类生物标志化合物,基于GDGTs的各种指标以其在指示物质来源以及海洋和陆地古温度重建等方面显示出的巨大应用潜力,逐渐成为古海洋学、古湖沼学和古气候学研究的重要工具。对采自东海陆架区的DH5-1站位(29°28.118′N、123°06.639′E,水深63.5m)的柱状沉积物样品进行了总有机质和GDGTs分析,研究了GDGTs化合物在东海陆架区柱状沉积物样品中的含量和沉积通量变化,并利用δ13 C、C/N以及基于GDGTs化合物的BIT指标讨论了该海区近150年来沉积有机质的来源变化。结果显示,近百年来东亚冬季风的增强,加强了冬季闽浙沿岸流对长江口沉积物的搬运,使得该海区陆源输入量呈增加趋势,但20世纪80年代以来,人类活动的加剧导致营养盐输入的增加,使得海洋生产力提高,沉积有机质中陆源有机质比例下降。 相似文献
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对采自冲绳海槽中部现代海底热液活动区的H9岩心沉积物进行了常量、微量元素分析,结果表明大部分元素含量在岩心75~80 cm处有一个明显的突变,上段中明显富集多种微量元素,这些元素正好对应于海槽中非热液活动区沉积物中相对亏损的元素,是热液活动区沉积物中的富集特征元素.75~80 cm处岩心沉积物中元素含量突变标志着冲绳海槽中部现代海底热液活动的开始或显著加强.除锰外,在其他热液活动区(如洋中脊等)显著富集的铁、铜、钴、镍在该区富集程度不高,但铅、鉮、锑、汞在上段岩心沉积物中的平均含量较下段高3~6倍,较非热液活动区沉积物中含量高3~12倍.这些富集元素与冲绳海槽热液活动成因硫化物中富集元素非常一致,表明该区热液活动对沉积物中锰、铅、鉮、锑、汞具有重要贡献,锰、铅、鉮、锑、汞是海槽中部现代海底热液活动的特征性示踪元素组合.岩心沉积物中很好地记录了热液活动的发展演化,该区海底热液活动从距今5740a开始发生或显著增强,并且一直持续到现在,只是其间活动程度经历了强弱变化,岩心上段锰的平均堆积速率约为40.461μg/(cm2·ka),与其他热液活动区的相当. 相似文献