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1.
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
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胶州湾沉积物中氨基酸对有机质降解及细菌源贡献的指示作用解析 总被引：2，自引：2，他引：0
基于对胶州湾表层沉积物中总可水解氨基酸（THAA）的含量、组成、构型及分布特征的系统研究，通过氨基酸碳氮归一化产率（THAA-C%，THAA-N%）、降解因子DI、反应活性指数RI以及D型氨基酸占比（D-AA%，摩尔百分比）等指标结合碳氮比（TOC/TN）、碳稳定同位素（δ13C）探析了胶州湾沉积物中有机质的来源与降解状态，利用细菌源有机质及胞外肽酶活性（EEA）探讨了微生物在有机质迁移转化过程中的作用与贡献。结果表明，胶州湾表层沉积物中氨基酸平均含量为（7.60±3.64）μmol/g，在陆源与海源混合影响下，其水平分布呈现湾内高于湾外、湾内东部高于西部的特点，表明湾内东部陆源输入对沉积物THAA具有较高贡献。THAA-C%、THAA-N%、DI、RI以及D-AA%等指示因子均显示胶州湾表层沉积物中有机质的降解程度呈现湾外高于湾内、湾内东部高于西部的变化趋势，有机质来源、微生物活性与上覆水水深共同影响了有机质的降解程度。胶州湾表层沉积物中细菌源有机碳的贡献率为（29.35±18.73）%，其水平分布显示出湾内西部与湾外相近且高于湾内东部的特点。细菌胞外肽酶活性（EEA）平均为（0.81±1.31）nmol/（g·h）（以MCA计），整体分布趋势与细菌贡献率相反，呈现湾内东部高于湾内西部和湾外的特性。沉积物中有机质的不同海源、陆源占比决定了有机质的可降解性，而有机质的降解程度进一步影响了细菌源有机质的贡献与胞外肽酶活性。 相似文献
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利用中国第18和21次南极考察获取的南极普里兹湾沉积物样品,分析了其中的有机碳和糖类物质的含量及组成,结果表明糖类和有机碳的分布受上层水体的初级生产、地形条件和水体垂直稳定度等多种因素的控制。表层沉积物中糖类物质的平均含量为3.03 mg/g,最高值为5.60mg/g,出现在湾内的毗邻陆架区。沉积物有机碳含量与表层海水叶绿素a具有良好的相关性,能够反映上层水体初级生产的变化。单糖组分的研究可以判定其生源母质,沉积物中有机质的来源主要是海洋上层生物。糖类是易被降解利用的有机质,通过糖类物质中六碳糖的比重及其垂直分布的变化可以判断出不同站位沉积速率的相对快慢。 相似文献
4.
南沙群岛西部海域两柱状沉积物中碳和氮的分布和来源特征及埋藏通量估算 总被引：6，自引：0，他引：6
对位于南沙群岛海域西部近大陆架-残留沉积区(NS01站)和深海沉积区(NS02站)的2个沉积物柱状样进行了研究,测定了它们的粒度组成、CaCO3含量、总有机碳含量(TOC)、总碳含量(TC)、总有机物含量(TOM)和总氮含量(TN),估算了它们的埋藏通量及陆/海源TOC和TN的相对含量.结果表明,该海域沉积物主要是粒径小于63μm的细粒度组分,粒度组成随深度的变化很小.沉积物粒度不是控制CaCO3含量、TOC、TC、TOM、TN和TOC/TN垂向变化的主要因素.NS01站CaCO3含量、TOC、TC、TOM和TN的含量及埋藏通量均低于NS02站.NS01站TOC/TN随深度的变化主要受控于TN的变化,而NS02站则主要受控于TOC的变化.2个研究站位的TOC和TN均以海洋自生为主,NS01站沉积物中海洋自生TOC和TN的平均值分别为53.2%和81.4%,NS02站沉积物中海洋自生TOC和TN的平均值分别为64.5%和87.7%. 相似文献
5.
山东半岛东北岸近海表层沉积物中木质素的分布特征及有机物来源 总被引：1，自引：0，他引：1
山东半岛东北岸近海是黄河入海泥沙向外输送的主要通道和重要沉淀区,探讨该海域沉积物中木质素的分布特征和有机物来源,对理解其中记录的环境演变信息具有重要意义.本文通过分析该海域表层沉积物中总有机碳(TOC)、总氮(TN)、碳稳定同位素(δ13C),并结合木质素及其特征参数,研究了其中有机物的来源,以及木质素的分布、植被来源和降解程度.结果表明,海源有机物是山东半岛东北岸近海表层沉积物中有机物的主要来源,有机物的分布特征受河流输入和海洋环流的共同影响.被子植物草本和木本组织是木质素的主要植被来源,酸醛比值表明表层沉积物中木质素都经历了较高程度的降解. 相似文献
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7.
环渤海地区河流河口及海洋表层沉积物有机质特征和来源 总被引：4，自引：0，他引：4
2013年8月采集了环渤海地区35条主要河流河口表层沉积物样品,12月采集了渤海与北黄海24个表层沉积物样品,分析了其生物地球化学指标:总有机碳(TOC)、总氮(TN)、有机碳同位素(δ13C)和氮同位素(δ15N),探讨该区域表层沉积物有机质特征及组成。研究表明:河流河口表层沉积物有机碳同位素(δ13C)值在–26.4‰—–21.8‰,平均值为–24.5‰;渤海表层沉积物有机碳同位素(δ13C)值在–23.8‰—–21.7‰,平均值为–22.3‰。河口表层沉积物TOC含量在0.06%—3.87%,平均值为1.31%;渤海表层沉积物TOC含量在0.52%—2.09%,平均值为1.08%。河流δ13C富集较轻,偏向陆源;海洋δ13C富集较重,偏向水生有机质来源。河流河口表层沉积物的δ13C值差异较明显,最大值与最小值相差4.6‰,但是流域地理位置距离近的河流δ13C值差异不大。河流河口表层沉积物δ15N在1.5‰—10.2‰,平均值为5.5‰;渤海表层沉积物δ15N在4.4‰—5.6‰,平均值为5.0‰。河流表层沉积物δ15N范围比渤海表层沉积物δ15N范围广,原因是河流受陆源有机物影响,且陆源有机物来源差异大。海洋表层沉积物δ15N相对均一,说明海洋表层沉积物δ15N受物源影响较小,体现了水体中有机质的转化和微生物活动对氮同位素的影响。本研究中表层沉积物的δ13C与δ15N没有明显的相关性,也体现了陆源有机质输入的影响。根据经典的二元模式计算,35条河流陆源有机质的贡献比例范围为10%—90%,平均值为60%;渤海陆源贡献比例范围为10%—50%,平均值为20%。河流有机质的来源以陆源有机质为主,水生有机质为辅。渤海有机质的来源以水生有机质为主,环渤海河流的陆源输入也有重要贡献。需要指出的是,有机碳同位素(δ13C)、氮同位素(δ15N)和Corg/Ntotal对有机质来源判别有一定局限性,虽然稳定同位素有示踪性,然而其成分仍然不可避免地受到生物地球化学等过程的改造,在使用稳定同位素技术示踪物源时,须小心谨慎。 相似文献
8.
环雷州半岛近海表层沉积物有机碳分布及其控制因素分析 总被引：1，自引：0，他引：1
对环雷州半岛近海43个海底表层沉积物的总有机碳(TOC)、总氮(TN)、沉积介质条件(包括沉积物粒度)进行了分析,探讨了沉积物TOC、TN的区域分布特征以及影响有机碳分布的主要因素。结果表明,环雷州半岛近海海域海底表层沉积物有机碳含量在0~0.79%之间,平均值为0.26%。与中国其它近海海域相比,环雷州半岛大部分近海区域海底表层沉积物有机碳含量明显偏低,为有机质贫乏区,仅雷州半岛西南部流沙湾近海海域为TOC相对高值区。总氮含量也不高,在0.011%到0.100%之间,TOC与TN存在较强的正相关性,且平面上TOC与TN分布高度重合,显示氮元素主要以有机化合物形式存在。TOC/TN比值在5.1~14.3之间,表明沉积有机质具有陆源输入和海洋自生来源的混合特征,但以雷州半岛西侧北部及东侧中部海域受陆源有机质输入影响更大。大多数站位海底沉积物粒度构成以粉砂为主、粘土次之,少数站位以砂质沉积为主。沉积物有机碳含量与粘土及粉砂含量呈弱正相关性,与沉积物pH值、Eh值及砂含量呈弱负相关性,这表明海底沉积物有机质丰度受有机质来源输入、海底氧化还原状态和沉积水动力条件(沉积物粒度)等因素综合控制。 相似文献
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湛江湾沉积物中酸可挥发性硫和重金属含量分布及重金属生态风险评价 总被引：2，自引：0，他引：2
测定了湛江湾海域20个站位表层沉积物中的酸可挥发性硫（AVS）、同步浸提重金属（SEM）、TOC含量和Eh值,对AVS、SEM含量的平面分布及AVS与SEM、TOC含量、Eh值的相互关系进行了分析.结果表明：该海域表层沉积物中AVS含量范围为0.004～0.547μmol/g,平均值为0.155μmol/g,SEM含量范围为2.10～4.27μmol/g,平均值为3.32μmol/g,相对其他海域湛江湾海域沉积物表现出AVS含量较低,SEM含量较高的特征.AVS与SEM含量平面分布较一致,湾顶的含量都较高,含量均值分别为0.361和3.52μmol/g,特呈岛以南到湾口呈逐渐减小的明显趋势.调查海域沉积物AVS与TOC含量呈显著正相关,与Eh值呈显著负相关,说明高有机质含量、低氧化还原电位沉积环境有利于AVS的生成.20个站位CSEM5-CAVS的差值均为0〈（CSEM5-CAVS）〈5,说明该海域可能存在重金属的中等毒性生态风险. 相似文献
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南海北部和海南岛附近海域表层沉积物中有机质的分布和降解状态的差异 总被引：3，自引：0，他引：3
利用气相色谱法对南海北部和海南岛附近海域表层沉积物中正构烷烃(n-alkanes)和脂肪酸进行测定和分析,结合粒径、比表面积(specific surface area,SSA)、有机碳(OC%)、碳稳定同位素(δ~(13)C)等参数研究有机物来源和降解状态,并对其影响因素进行分析。研究结果表明:沉积物主要以粉砂为主,平均粒径分布范围在10.97—517.21μm之间,选取的16个站位的比表面积平均值为8.05m~2/g,最大值是S23站位的24.46m~2/g,最小值是S29站位的1.73m~2/g,OC%含量在0.15—1.18之间,δ~(13)C值为–23.05‰—–21.24‰。沉积物中正构烷烃碳链的分布范围是nC_(14)—nC_(33),低碳数峰群以nC_(16)、nC_(18)为主峰碳且具有偶碳数优势,高碳数峰群以nC_(29)为主峰碳。脂肪酸的碳数分布范围是nC_(14)—nC_(30),低碳数单峰型分布,短链饱和脂肪酸(short chain saturated fatty acids,SCSFA)和单不饱和脂肪酸(monounsaturated fatty acids,MUFA)的含量占总脂肪酸含量的70%以上,长链饱和脂肪酸(long chain saturated fatty acids,LCSFA)的含量不到10%,据此说明这两个区域有机质均以海源输入为主。在有机物保存和降解方面,海南岛附近海域有机质载荷(OC/SSA)和δ~(13)C之间的正相关,表现了良好的陆源和海源的有机物更替,但是珠江口附近海域系列样品却未见相似过程。不仅在物源更替方面,在有机质降解特征上珠江口附近海域中的有机物与海南岛附近海域和南海陆架深水区也有很大的差别。海南岛附近海域和南海陆架深水区有机质的降解符合一般规律,随着水深的增加降解程度逐渐变大,然而珠江口附近海域随着水深的增加有机质却越来越"新鲜"。结合前人对珠江口附近海域黏土矿物组成的研究,本文认为珠江口附近海域沉积物中有机质之所以会出现上述"异常"可能是因为该研究区域黏土矿物对有机质选择性吸附所导致。 相似文献
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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
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《Deep Sea Research Part I: Oceanographic Research Papers》2001,48(3):811-832
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
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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
14.
辽河口芦苇湿地土壤有机碳的积累特征研究 总被引：1，自引：0，他引：1
通过研究辽河口芦苇湿地土壤有机碳、石油类、阴离子表面活性剂(LAS)、多环芳烃(PAHs)及脂肪酸的垂直分布特征,探讨了不同来源有机物在芦苇湿地的埋藏和降解规律.土壤样品采集于2009年3月,研究发现,有机碳含量范围为0.3％～9.3％,石油烃含量范围为19.04～482.31mg/kg(干重)之间,LAS含量范围为0.84～19.28mg/kg(干重),PAHs含量范围为2.59～4.40 mg/kg(干重).总脂肪酸含量范围为5.72～190.69mg/kg(干重).表层有机碳含量丰富,来源广泛.辽河油田不同年代的采油环保措施可能是芦苇湿地土壤中石油类聚集量多寡的主要因素,芦苇根际的调控调节作用和微生物的选择性降解也对土壤石油类化合物分布起到重要作用.LAS含量从土壤表层向下迅速降低了67.0％,是所研究有机物中降解最迅速的一种.PAHs自表层至底层没有明显的变化趋势.细菌是辽河芦苇湿地土壤有机碳再生产的主要承担者,在次表层以下,细菌生产所利用的有机碳主要来自现场的生产. 相似文献
15.
《Marine Chemistry》2001,73(1):65-81
Radiocarbon (Δ14C) abundance and stable carbon isotope (δ13C) compositions were measured for total lipid, total hydrolyzable amino acids (THAA), total carbohydrates (TCHO), and acid-insoluble organic fractions separated from phytoplankton, zooplankton, and sediment cores collected from two abyssal sites, one in the northeast (NE) Pacific Ocean and one in the Southern Ocean. These results are compared with those obtained for a separate core from the NE Pacific and reported by Wang et al. [Geochim. Cosmochim. Acta 62 (1998) 1365.]. An uncharacterized acid-insoluble fraction dominated (43–57%) the sediment TOC pool at both sites. Sediment collected from the NE Pacific exhibited higher TOC, TN. and higher Δ14C values and contained both labile (THAA and TCHO) and refractory (lipid and acid-insoluble) fractions. In contrast, sediment from the Southern Ocean had much lower TOC and Δ14C values, which indicated that organic matter was extremely refractory. Sedimentation rates calculated from 14C ages of TOC for both sites indicate that the differences in the organic composition and Δ14C signatures of organic matter in the sediments likely resulted from the differences in production and deposition of organic matter to the sediment, and the diagenetic stages of sedimentary organic matter in the two oceans.Unlike Δ14C, stable carbon isotopic (δ13C) compositions of TOC in the sediments of the two oceans had similar values, which reflect not only the organic matter input from marine-derived sources but also the nature of degraded, predominately uncharacterized organic fraction in these sediments. The differences in δ13C values among the compound classes in sediments at both sites can be attributed to the carbon isotopic signatures in original sources during photosynthesis and associated environmental factors. Preferential degradation of organic matter and heterotrophic effects may also play important roles for the observed δ13C variations and these effects need to be further investigated. 相似文献
16.
高效毛细管电泳法测定海参多糖的单糖组成 总被引：1，自引：0，他引：1
目的:采用高效毛细管电泳法测定3种不同海参多糖的单糖组成。方法:海参多糖水解后,经PMP衍生化,高效毛细管电泳分析。电泳条件:缓冲液为60 mmol.L-1硼砂溶液(pH=9.0);柱温25℃;运行电压25 kV;检测波长245 nm;压力进样50 mbar,进样时间5 s。结果:3种不同海参多糖中均含GalN、GlcN、GalNAC、Glc、Man、Fuc、Gal、GlcUA,梅花参多糖中各单糖的摩尔比为1.00∶1.02∶1.63∶1.19∶1.02∶10.26∶0.82∶0.38,四方刺参多糖中各单糖的摩尔比为1.00∶0.41∶0.43∶0.56∶0.29∶5.47∶0.43∶0.25,北极参多糖中各单糖的摩尔比为1.00∶0.26∶0.22∶0.25∶0.06∶1.36∶0.27∶0.16。结论:该方法具有简单、快速、分离效率高等特点,能同时测定海参多糖中氨基糖、中性糖、糖醛酸的组成。 相似文献
17.
Sediment and water column data from four sites in North, Central and South San Francisco Bays were collected monthly from November 1999 through November 2001 to investigate the seasonal variation of benthic organic matter and chlorophyll in channel sediments, the composition and quality of sediment organic matter (SOM), and the relationship between seasonal patterns in benthic organic matter and patterns in water column chlorophyll. Water column chlorophyll peaked in the spring of 2000 and 2001, characteristic of other studies of San Francisco Bay phytoplankton dynamics, however an unusual chlorophyll peak occurred in fall 2000. Cross-correlation analysis revealed that water column chlorophyll at these four channel sites lead sediment parameters by an average of 2 to 3 months. Sediment organic matter levels in the San Francisco Bay channel showed seasonal cycles that followed patterns of water column production: peaks in water column chlorophyll were followed by later peaks in sediment chlorophyll and organic matter. Cyclical, seasonal variations also occurred in sediment organic matter parameters with sediment total organic carbon (TOC) and total nitrogen (TN) being highest in spring and lowest in winter, and sediment amino acids being highest in spring and summer and lowest in winter. Sediment chlorophyll, total organic carbon, and nitrogen were generally positively correlated with each other. Sediment organic matter levels were lowest in North Bay, intermediate in Central Bay, and highest in South Bay. C:N ratio and the ratio of enzyme hydrolyzable amino acids to TOC (EHAA:TOC) data suggest that SOM quality is more labile in Central and northern South Bay, and more refractory in North Bay and southern South Bay. 相似文献
18.
Spatial and temporal variations of sedimented organic matter in Xiaohai Lagoon, Hainan Island 总被引：1，自引：1，他引：0
The characteristics of grain-size,total organic carbon(TOC) and total nitrogen(TN) contents,TOC/TN ratios,stable carbon isotope(δ13C) and 210 Pb dating were measured in six sediment cores from the Xiaohai Lagoon.The results show distinct spatial and temporal variations in sedimentation patterns.The sediments are dominated by clayey silt,sandy silt and by silty sand in the southern,middle lagoon and the northern lagoon,respectively.TOC and TN contents decline from south to north.Sedimentation rates,determined by 210 Pb dating,tend to decrease from south to middle.However,the determination of sedimentation rate in the north is difficult.These spatial variations are related to the variations in sediment sources and hydrodynamic conditions in the Xiaohai Lagoon.The variations of organic matter signatures can be divided into two stages in the cores from the southern and middle lagoon.Before 1988,the organic matter signatures are relatively stable.The contribution of terrestrial organic carbon sources varies between 60% and 85%.After 1988,the organic matter signatures demonstrate significant variations.TOC and TN contents increase rapidly,TOC/TN ratios decrease,δ13C values shift to higher and the contribution of terrestrial organic carbon sources decreases to 40%-50%.The contributions of phytoplankton organic matter have increased in the sediment since 1988.Increasing aquaculture activities have had a significant impact on organic matter signatures since 1988.The sedimentation rates have increased rapidly in the southern and middle lagoon since 1988 due to the anthropogenic activities which include aquaculture,mining and deforestation.These activities have caused eutrophication and increased siltation in the southern and middle lagoon. 相似文献