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1.
铁作为地壳中丰度最高的元素之一,广泛参与到一系列地球化学循环中。现代海洋中的铁主要来源于河流、冰川和风的铁氧化物颗粒和溶解铁的输入。陆源输入的铁氧化物在有机质埋藏、降解的早期成岩作用过程中,发生一系列转化过程而埋藏下来,该过程被称作活性铁循环。氧化 强氧化条件利于沉积物中氧化铁的持续产生或者至少保持不被溶解的状态,从而形成棕色-红色沉积物;还原条件利于沉积物中铁氧化物的溶解,形成菱铁矿、黄铁矿(铁硫化物) 等形式的埋藏,并可能造成溶解铁在海洋内的迁移。Raiswell、Canfield、Poulton等通过对现代典型海洋环境活性铁循环研究,提出了一系列用于判别古海洋氧化 还原条件的活性铁指标体系,并成功地将太古宙以来的古海洋划分成为含铁的大洋、硫化的大洋和氧化的大洋等3个演化阶段。由于活性铁的不同形态对磷具有不同的生物地球化学效应,将造成“氧化条件下磷的优先埋藏、缺氧条件下优先释放的现象”。磷是海洋生产力的限制性元素,铁和磷循环的上述耦合关系将造成“缺氧的大洋生产力越高,富氧的大洋生产力越低”现象的出现。目前已在白垩纪古海洋缺氧 富氧沉积中初步证实了上述反馈关系的存在,但是对活性铁埋藏形式对该特殊沉积的贡献还需要进一步的工作。 相似文献
2.
太湖及其主要入湖河流沉积磷形态分布研究 总被引：57，自引：6，他引：57
选择了我国第三大浅水湖泊--太湖及其主要入湖河流进行沉积磷形态的连续提取研究.太湖湖区沉积磷中不稳态磷(LP)及铝结合态磷(Al-P)含量很低,其余形态磷为铁结合态磷(Fe-P)＜钙结合态磷(Ca-P)＜有机磷(Org-P).河流沉积物中有机磷的相对含量高于湖泊沉积物,绝对含量平均值约为湖泊沉积物的3.9倍,铁结合态磷的绝对含量约为湖泊沉积物的3/4,湖区沉积物Fe-P含量与水体中PO3-4-、Chla呈显著正相关关系,同时与间隙水的氧化性呈显著负相关关系.太湖各湖区沉积物的磷形态表现为空间差异较大,活性组分的差异性要大于活性较差的组分.总的来说北部湖区沉积物中Fe-P和Org-P含量高于其他湖区,这与太湖北部湖区水体高营养级和藻类爆发关系密切.湖区沉积磷的垂直分布规律较复杂,既有随深度增加的,也有随深度降低的,河流沉积物同样如此.这与太湖及河流生态条件、污染物排放以及沉积动力学条件不同有关. 相似文献
3.
北京官厅水库沉积物-水界面磷的分布和迁移特征 总被引：2，自引：0，他引：2
研究官厅水库一个沉积物柱及上覆水体磷的含量和形态特征,指出水体中的磷以颗粒态为主,界面上覆水中磷以无机磷酸盐为主,孔隙水中以有机磷占优势;界面附近湖水中总溶解磷、总无机磷、正磷酸盐和有机磷酸盐从远离界面到界面逐渐升高,孔隙水中总溶解磷、总无机磷、正磷酸盐在界面下10 cm左右达到最大值,有机磷含量由界面向下有增加趋势;计算了沉积物-水界面磷的沉降和扩散通量,分别为1967.5μg/a@cm2和0.5μg/a@cm2,结合沉积物中矿物组成、磷与Fe、Mn、SO2-4的关系,探讨影响磷分布和迁移的影响因素. 相似文献
4.
对沉积物再悬浮的驱动力及其耦合效应、再悬浮-内源磷迁移转化机制及主要影响因素进行了阐述,探讨了该领域未来可能的研究方向。相关研究发现,沉积物再悬浮的各种驱动力既可以单独作用也可相互耦合,其耦合效应具有显著的时空变异性;再悬浮使还原态沉积物暴露于有氧环境,沉积物中铁、锰的氧化以及沉积物颗粒的吸附促进了内源水溶态无机磷(SRP)的去除,而进入水体的内源有机磷则通过生物矿化和光化学分解转化为SRP;沉积物物化特征、水动力、水生生物以及水体理化性质等因素控制着再悬浮过程中内源磷的迁移和转化。指出再悬浮条件下沉积物内源磷迁移转化的多过程耦合效应、沉积物中磷形态的转化及其生物有效性、内源有机磷矿化与光化学分解机制及其调控因素将是本领域需要进一步研究的重点。 相似文献
5.
《地质科技情报》2015,(5)
水土界面氟的迁移对高氟地下水的形成具有重要影响。以大同盆地典型氟中毒区为例,分析了不同岩性沉积物中的氟质量分数和形态分布特征,并通过室内静态实验,探究了水溶液的pH值、Ca2+、HCO-3以及H2PO-4质量浓度对水土界面氟迁移的影响。研究结果表明,沉积物中不同形态氟按含量由高到低的顺序依次为:残余态氟铁锰氧化态氟水溶态氟有机束缚态氟离子交换态氟;各形态氟在不同岩性沉积物中含量大小均表现为:黏土粉质黏土粉砂;在沉积物中,黏土矿物和方解石是主要的固氟矿物成分。溶液的pH值、Ca2+、HCO-3以及H2PO-4质量浓度与氟在沉积物表面的吸附-解吸和沉淀-溶解平衡密切相关,沉积物对氟的吸附量随溶液pH值和HCO-3质量浓度增大而降低,随Ca2+和H2PO-4质量浓度增大而增大。 相似文献
6.
三江平原土地利用变化对水体中铁环境行为的影响 总被引：1，自引：0，他引：1
三江平原湿地农田化对铁的赋存形态、迁移转化特征及输出量产生影响。以湿地沼泽水体和稻田水体为研究对象,利用切向超滤技术分离铁的形态,研究土地利用变化前后铁的形态、迁移转化特征的差异。结果表明：湿地农田化后水体中可溶态总铁质量浓度下降16.9%;由于水体pH值的升高,Fe2+质量浓度下降56.3%,非溶解态酸性不稳定铁含量显著升高。沼泽水和稻田水在迁移过程中,铁均以络合态铁和酸性不稳定态铁2种形态迁移。沼泽水在迁移过程中Fe2+和络合态铁含量下降,酸性不稳定态铁含量升高,胶体态铁含量变化不大;稻田水在迁移过程中,络合态铁和酸性不稳定态铁含量下降,Fe2+和胶体态铁含量较稳定。2种水体铁形态的转化有较大差异：日间沼泽水中非溶解态的酸性不稳定态铁向可溶态铁转化;稻田水体可溶态铁向酸性不稳定态铁转化。 相似文献
7.
通过在滇池开展原位实验,研究探讨了湖泊沉积物中磷灰石制约水铁矿分解和转化的机制,以及二者共存时的环境效应。结果表明:将水铁矿放置到沉积物中1个月,矿物保持稳定;放置时间达到3个月时,添加磷灰石实验中水铁矿发生了显著物相转变。冬天(12—2月)实验中,转化产物随深度的变化趋势为针铁矿+磁(赤)铁矿→针铁矿+纤铁矿→针铁矿;夏天(6—9月)实验中,转化产物随深度的变化趋势为针铁矿+纤铁矿+磁(赤)铁矿→针铁矿+纤铁矿→未转化。透射电镜分析结果显示冬天实验中生成的磁性铁氧化物为纳米磁铁矿和磁赤铁矿,夏天实验中产生的则主要为纳米磁铁矿。X射线光电子能谱分析结果显示冬天表层实验样品具有较高P含量。分析表明的湖泊沉积物中磷灰石促进水铁矿转化的过程为:(1)微生物促进磷灰石溶解;(2)磷灰石溶解释放的P促进铁还原菌生长;(3)铁还原菌促进水铁矿还原;(4)水铁矿还原产生的溶解态Fe2+催化水铁矿向针铁矿、纤铁矿和磁铁矿转化。冬天及沉积氧化-还原界面最适宜磷灰石分解菌和铁还原菌生长,水铁矿的转化和P释放能力也更强,相应地内源磷释放的风险也更大。 相似文献
8.
水体中富营养化水平与磷元素的赋存形态密切相关。目前围绕引起富营养化关键因子之一的磷形态的垂向分布特征、各磷形态间的迁移转化行为及其影响因素取得了比较明确的研究进展。为进一步揭示不同磷形态在沉积物-水体系中迁移转化行为随时空的变化特征,本文采用磷钼蓝分光光度法对沱江流域简阳段间隙水中可溶性活性磷(SRP)、可溶性非活性磷(SUP)及总溶解性磷(TDP)进行测定;采用SMT法和改进的沉积物无机磷形态连续提取法对沉积物中总无机磷(TIP)、总磷(TP)、难提取磷(Res-P)、可交换态磷(Exc-P)、铁结合态磷(Fe-P)、铝结合态磷(Al-P)、钙结合态磷(Ca-P)进行提取,磷钼蓝分光光度法进行测定,以揭示沉积物-水体系中磷的赋存形态垂向分布行为特征,并将实验数据与十年前该地区磷的赋存形态结果进行对比,探讨磷赋存形态的变化趋势及影响因素。结果表明:间隙水中SRP、SUP和TDP的含量分别为0.004～0.36mg/L、0.080～3.19mg/L和0.056～3.28mg/L;沉积物中TP、TIP、Res-P、Exc-P、Al-P、Ca-P含量分别为1235.40～1646.94mg/kg、860.00～1318.59mg/kg、130.31～537.13mg/kg、1.35～14.10mg/kg、0.007～0.12mg/kg、743.13～1109.91mg/kg,Fe-P未检出。对比十年前后沉积物-水体系中磷赋存形态的变化可知,由于受到外源磷输入的影响,间隙水中SRP、SUP以及TDP含量虽然在-10cm以上变化不明显,但在-10cm以下明显增大,且导致沉积物中TP、TIP含量增加;偏碱性的沉积环境导致Al-P的释放,其含量明显减小;Exc-P含量的减小与其转化为稳定的Ca-P或Res-P形态有关。研究认为:随着时空的变化,沱江简阳段沉积物呈现外源磷输入和内源磷释放的综合污染。总体而言,由于输入的磷形态大部分以稳定的Ca-P和Res-P形态存在于沉积物中,使得表层间隙水中生物可直接利用的磷含量总体变化不大,该地区富营养化程度不会加重。维持沉积环境的弱碱性,有利于Al-P、Exc-P等向Ca-P的有效转换,抑制河流富营养化。 相似文献
9.
为探析长江口沉积物-水界面砷的迁移转化机制,本文分析了2019年夏季长江口4个站位上覆水和间隙水中总As浓度及形态的剖面变化特征,耦合氧化还原敏感元素(Fe、Mn和S)的剖面变化剖析了沉积物-水界面砷循环的Fe-Mn-S控制机制,同时结合砷相关功能基因探讨了沉积物-水界面砷迁移转化的微生物调控过程,估算了沉积物-水界面总As的扩散通量。结果表明,除A7-4站位外,长江口其他3个站位间隙水总As以As3+为主要存在形态,且总As浓度均在上覆水中为最低值(0.748~1.57 μg·L-1),而在间隙水中随着深度增加而逐渐增加并在6~9 cm深度达到峰值(7.14~26.9 μg·L-1)。间隙水总As及As3+浓度的剖面变化趋势与溶解态Fe2+、Mn2+相似,其均在中间层出现高值,说明沉积物Fe/Mn还原带砷的释放可能是随固相Fe(Ⅲ)或Mn(Ⅳ)的还原而转移到间隙水中的。氧化层和Fe/Mn还原带过渡区间隙水砷浓度与砷异化还原菌功能基因arrA和arsC丰度存在对应关系(除A1-3站外),说明砷异化还原菌将溶解As5+或固相As5+还原为溶解As3+可能是该过渡层砷迁移转化的另一重要过程。硫酸盐还原带的间隙水总As和As3+浓度降低,但由于间隙水的低S2-浓度不利于砷硫化物生成,因此深层间隙水砷可能与铁硫矿物结合而被移除。底层环境氧化还原条件是影响沉积物-水界面砷迁移转化的重要因素,随底层水DO浓度的降低,砷迁移转化更倾向于微生物还原控制。长江口沉积物-水界面总As的扩散通量为1.18×10-7~2.07×10-7 μmol·cm-2·s-1,均表现为沉积物间隙水中总As向上覆水释放,即沉积物是研究区域水体总As的来源之一。 相似文献
10.
云南滇池微生物对磷循环与沉积作用的实验研究 总被引：6，自引：0，他引：6
对滇池磷的现代沉积作用的研究中发现,滇池微生物种群和数量繁多,但能对磷溶解、转化、迁移、聚集、沉积的微生物主要有解磷菌和聚磷菌两类。在底泥磷高含量区域,解磷菌的种群和数量与底泥磷含量成负相关关系,与水体磷含量成正相关关系,而聚磷菌的种群和数量与底泥磷含量成正相关关系,与水体磷含量成负相关关系;在底泥磷低含量区域,上述相关性则相反。表明当解磷菌的种群与繁衍量大于聚磷菌的种群和繁衍量时,底泥中的磷向水体迁移,反之,水体中的磷向底质迁移、聚集。这个事实令人信服的证明了微生物对磷循环的重要作用。滇池这种活着的微生物在自然环境条件下对磷的溶解、转化、迁移、聚集和沉积的作用,对古磷块岩微生物成矿说提供了可靠的证据,且对以磷为限制性因子的湖、海、江河环境污染的防治提供了理论资料。 相似文献
11.
边缘海沉积物是海洋重要的碳储库,其内部的碳循环主要是由有机质矿化分解过程来驱动的。有机碳进入边缘海沉积物后,矿化分解为溶解无机碳(DIC)进入沉积物孔隙水并扩散到上层水柱,参与海洋系统碳循环;同时还有部分DIC与钙镁等离子结合形成自生碳酸盐,保存于沉积物碳库。从生物地球化学角度探讨有机质埋藏机制和效率,在此基础上重点综述沉积物硫酸盐还原、产甲烷和甲烷厌氧氧化过程的耦合机制,以及有机质矿化对自生碳酸盐形成的影响等方面的研究进展,以期加深对陆架边缘海沉积物在全球碳循环收支平衡中的作用及其气候环境效应的认识。 相似文献
12.
Using some uranium deposits and recent U-bearing sediments as examples, it is shown that all U-bearing rocks are characterized by an association of organic matter and calcium phosphate, irrespective of the quantitative relationship between these components. A considerable proportion of these components was delivered into sediments with remains of marine planktonic and nektonic organisms. Along with organic matter, calcium phosphate played a significant role in uranium concentration. This is related to a high sorption ability of the calcium phosphate. Uranium accumulated during diagenesis as a result of diffusion exchange between bottom and interstitial waters. The combination of anoxic bottom environment with high bioproductivity in upper aerated waters, a typical phenomenon in oceanic upwelling zones, is the most favorable factor of uranium concentration in the sedimentary process. This determines the stable paragenetic association of organic matter, phosphorus, and uranium in marine sediments, such as black shales and organogenic phosphate deposits. 相似文献
13.
Continental margin sediments are important ocean carbon repository, and the internal carbon cycle is mainly driven by the mineralization processes of sedimentary organic matter. Most organic carbon is transformed to Dissolved Inorganic Carbon (DIC) by mineralization processes after being delivered to continental margin sediments, and DIC from pore water diffuses into the upper water column and participates in the ocean carbon cycle. At the same time, some DIC combines ions such as Ca2+ and Mg2+ and precipitates as authigenic carbonate minerals so that carbon is stored in the deposits. Based on the biogeochemical study of the mechanism and efficiency of organic matter burial, we discussed the interaction among sulfate reduction, methanogenesis and anaerobic oxidation of methane, and the effect of organic mineralization on the formation of authigenic carbonate. By reviewing the above-mentioned aspects, we can obtain a better understanding of the role of continental margin sediments in the global carbon cycling budgets as well as its climate and environmental effects. 相似文献
14.
JOÃO TRABUCHO ALEXANDRE JUAN PEDRO RODRÍGUEZ‐LÓPEZ POPPE L. DE BOER 《Sedimentology》2011,58(5):1217-1246
The Aptian/Albian oceanic anoxic event 1b contains the record of several perturbations in the global carbon cycle and multiple black shale levels, particularly in the Western Tethys. The local lithological expression of an oceanic anoxic event depends on palaeogeographical and depositional setting as well as on regional palaeoclimate. Marine sediments at a particular location may therefore be more or less organic‐rich (or not at all) and they may consist of different lithologies. In most studies, however, much of the lithological variability associated with oceanic anoxic events is left unaccounted for and, thus, the exact processes leading to the enrichment of organic matter in these marine sediments and their subsequent preservation in the geological record are unknown. This study focuses on the local sedimentary processes behind the deposition of organic‐rich sediments at Deep Sea Drilling Project Site 545 and Ocean Drilling Program Sites 1049 and 1276 in the North Atlantic during oceanic anoxic event 1b. Although specifically dealing with the sediments deposited during this particular event at these localities, it is expected that the same processes were responsible for determining the exact sedimentary products at localities in similar settings, as well as during other similar events in the Mesozoic. Here, it is shown that the deposition of organic‐rich sediments during oceanic anoxic event 1b was a consequence of the enhanced productivity favoured by upwelling and by riverine nutrient input, or aeolian fertilization of the euphotic zone depending on geographical location. Slope instability processes resulted in the transfer of part of these organic‐rich sediments from the shelf to deep sea depocentres as mud‐laden organic‐rich turbidites, especially in the northern North Atlantic. The so‐called ‘black shales’ are much more varied than their name implies. The end product of sedimentation during an oceanic anoxic event at a particular location is commonly the result of several equifinal processes acting on a local scale rather than the direct result of basinal or even global mechanisms. 相似文献
15.
The fractionation of P in Pandoh Lake surface sediments has been investigated for the first time in order to understand its environmental availability and sources, and the eutrophication status of this lake. Inorganic-P is present mainly as authigenic-P (step-III). The authigenic P concentration is higher in winter relative to the summer and monsoon seasons and ranged from 35.9 to 46.9 μg/g. The loosely sorbed or exchangeable-P (step-I), Fe(III)-bound-P (step-II) and detrital inorganic-P (step-IV) were higher in the monsoon season and varied from 3.70 to 11.1 μg/g, 16.9 to 32.0 μg/g and 9.89 to 17.0 μg/g, respectively. Organic-P reached a maximum in the summer season and ranged from 8.00 to 14.9 μg/g. Authigenic-P and detrital inorganic-P show seasonal changes, as pH influences the interaction between P and CaCO3 in the water column. In the winter season, phosphate is precipitated out of the water column and fixed in the sediments as a result of an increase in pH. Calcite-bound-P in the sediments may be redissolved by decreasing pH in the summer season. Relatively high rates of mineralization during the monsoon results in the seasonal pattern of organic-P fractionation to sediment as follows: monsoon = winter < summer. Iron, Ca, organic matter and silt and clay contents seem to play a significant role in regulating the seasonal P budget. Principal component analysis (PCA) was used to identify the factors which influence sedimentary P in the different seasons. 相似文献
16.
扬子地块北部被动边缘的南秦岭古生代沉积盆地中,发育一套自早古生代—中生代以来的碳酸盐岩夹细碎屑岩沉积建造,形成规模巨大独具特色的以铅锌金为主的多金属成矿带。伸展构造体制下形成的裂陷或断陷型盆地中,正常水成沉积与热水沉积同盆共存。正常水成沉积中叠加的热水沉积是一个"突发事件或灾变事件",具有特殊的物质组成和产态。通过对区内沉积成矿盆地的识别、分级,二级沉积盆地中边缘部位常发育多个三级构造热水沉积成矿盆地,它受控于沉积盆地中的同生断裂,具有沉积岩相、热水沉积岩组合、显著成矿作用及物化探异常广布的特点。三级构造热水沉积成矿盆地是矿床定位的构造空间,四级热水沉积洼地为矿体(矿层)的容纳空间。区内热水沉积岩主要为重晶石(毒重石)岩、硅质岩、钠长石岩和铁碳酸盐岩类,铅锌重晶石等矿产多产于热水沉积岩中或上盘。热水沉积形成一般由早期的热水喷发交代→主期热水喷流→晚期热水喷气演变。早期的热水喷发交代往往沿矿液喷发通道,形成网脉状、角砾状矿化;主期热水喷流主要形成多金属及热水喷流相,形成块状、条带状、层纹状矿石或热水沉积岩;晚期热水喷气主要形成浸染状矿石和热水喷气岩石。 相似文献
17.
Phosphate oxygen isotopes: Insights into sedimentary phosphorus cycling from the Benguela upwelling system 总被引：1，自引：0，他引：1
Tobias Goldhammer Benjamin Brunner Stefano M. Bernasconi Matthias Zabel 《Geochimica et cosmochimica acta》2011,75(13):3741-3756
Marine sediments are the main sink in the oceanic phosphorus (P) cycle. The activity of benthic microorganisms is decisive for regeneration, reflux, or burial of inorganic phosphate (Pi), which has a strong impact on marine productivity. Recent formation of phosphorites on the continental shelf and a succession of different sedimentary environments make the Benguela upwelling system a prime region for studying the role of microbes in P biogeochemistry. The oxygen isotope signature of pore water phosphate (δ18OP) carries characteristic information of microbial P cycling: Intracellular turnover of phosphorylated biomolecules results in isotopic equilibrium with ambient water, while enzymatic regeneration of Pi from organic matter produces distinct offsets from equilibrium. The balance of these two processes is the major control for δ18OP.Our study assesses the importance of microbial P cycling relative to regeneration of Pi from organic matter from a transect across the Namibian continental shelf and slope by combining pore water chemistry (sulfate, sulfide, ferrous iron, Pi), steady-state turnover rate modeling, and oxygen isotope geochemistry of Pi.We found δ18OP values in a range from 12.8‰ to 26.6‰, both in equilibrium as well as pronounced disequilibrium with water. Our data show a trend towards regeneration signatures (disequilibrium) under low mineralization activity and low Pi concentrations, and microbial turnover signatures (equilibrium) under high mineralization activity and high Pi concentrations. These findings are opposite to observations from water column studies where regeneration signatures were found to coincide with high mineralization activity and high Pi concentrations. It appears that preferential Pi regeneration in marine sediments does not necessarily coincide with a disequilibrium δ18OP signature. We propose that microbial Pi uptake strategies, which are controlled by Pi availability, are decisive for the alteration of the isotope signature. This hypothesis is supported by the observation of efficient microbial Pi turnover (equilibrium signatures) in the phosphogenic sediments of the Benguela upwelling system. 相似文献
18.
本文以前人对西秦岭地区地层、岩相及有机地球化学研究成果为基础,结合补充的实际资料,论述了生物礁与西秦岭铅锌矿的伴生关系及其成因联系.地质建造上,规模矿床赋矿地层的共同特点是相对发育灰岩及生物灰岩;空间上,生物礁为沉积成矿洼地的障壁;层序上,沉积型铅锌矿和改造型铅锌矿与生物礁的伴生关系有所不同,前者一般赋存于生物灰岩或碎屑岩中,后者的矿体常赋存在生物灰岩与泥质岩的过渡部位,表现为礁硅岩套.与造礁生物有关的有机质可能在沉积成矿或改造成矿作用发生前的成岩过程中,参与了硫酸盐的热化学还原及铅、锌等多金属元素的萃取、运聚过程.板内伸展阶段的深源流体、陆内俯冲阶段的深源或岩浆热液注入先存的中低温富有机质卤水,分别导致了沉积和改造成矿作用发生.沿生长断裂发生的热水沉积成矿作用促进了处于低纬度地区的生物礁生长,并形成成矿洼地的障壁.生物礁在改造成矿过程中的作用主要在于形成利于改造成矿作用发生的成矿构造. 相似文献
19.
沉积盆地动力学与盆地流体成矿 总被引：13，自引：1，他引：12
刘建明 《矿物岩石地球化学通报》2000,19(2):76-84
沉积盆地实际上是地球动力学系统中一个巨大的动态化学反应器,其所处的地球动力学背景制约着它的边界条件、外部环境及其与外部环境的物质和能量交换。盆地内则是一个由固体无机,有机沉积物颗粒和盆地流体组成的多相反应体系,包括各种流-岩-烃及流-流反应、与有机质成熟演化有关的各种有机反应、在浅部还有细菌参与的生物化学反应。体系的上部边界不断有新沉积物颗粒和流体的加入,下部则有来自基底的流体或来自盆地边缘大气降水的加入循环,同时还有盆地的构造沉降和基底热能的交换,以及可能岩浆物质,能量的加入。沉积物的固结成岩和后生变化,以及其中储存的油气和金属矿床都是这个巨型化学反应器的一部分(并非全部)产物。因此,只有站在盆地动力学的高度,才可能从整体上去认识这些共存的复杂因素和作用过程的耦合关系,才可能从本质上理解有关矿床的形成机理和产出规律。 相似文献
20.
A quantitative reconstruction of organic matter and nutrient diagenesis in Mediterranean Sea sediments over the Holocene 总被引：2，自引：0，他引：2
Daniel C. Reed Caroline P. Slomp Gert J. de Lange 《Geochimica et cosmochimica acta》2011,75(19):5540-5558
A multicomponent diagenetic model was developed and applied to reconstruct the conditions under which the most recent sapropel, S1, was deposited in the eastern Mediterranean Sea. Simulations demonstrate that bottom waters must have been anoxic and sulphidic during the formation of S1 and that organic matter deposition was approximately three times higher than at present. Nevertheless, most present day sediment and pore water profiles — with the exception of pyrite, iron oxyhydroxides, iron-bound phosphorus and phosphate — can be reproduced under a wide range of redox conditions during formation of S1 by varying the depositional flux of organic carbon. As a result, paleoredox indicators (e.g., Corg:S ratio, Corg:Porg ratio, trace metals) are needed when assessing the contribution of oxygen-depletion and enhanced primary production to the formation of organic-rich layers in the geological record. Furthermore, simulations show that the organic carbon concentration in sediments is a direct proxy for export production under anoxic bottom waters.The model is also used to examine the post-depositional alteration of the organic-rich layer focussing on nitrogen, phosphorus, and organic carbon dynamics. After sapropel formation, remineralisation is dominated by aerobic respiration at a rate that is inversely proportional to the time since bottom waters became oxic once again. A sensitivity analysis was undertaken to identify the most pertinent parameters in regulating the oxidation of sapropels, demonstrating that variations in sedimentation rate, depositional flux of organic carbon during sapropel formation, bottom water oxygen concentration, and porosity have the largest impact. Simulations reveal that sedimentary nutrient cycling was markedly different during the formation of S1, as well as after reoxygenation of bottom waters. Accumulation of organic nitrogen in sediments doubled during sapropel deposition, representing a significant nitrogen sink. Following reventilation of deep waters, N2 production by denitrification was almost 12 times greater than present day values. Phosphorus cycling also exhibits a strong redox sensitivity. The benthic efflux of phosphate was up to 3.5 times higher during the formation of S1 than at present due to elevated depositional fluxes of organic matter coupled with enhanced remineralisation of organic phosphorus. Reoxygenation of bottom waters leads to a large phosphate pulse to the water column that declines rapidly with time due to rapid oxidation of organic material. The oxidation of pyrite at the redox front forms iron oxyhydroxides that bind phosphorus and, thus, attenuate the benthic phosphate efflux. These results underscore the contrasting effects of oxygen-depletion on sedimentary nitrogen and phosphorus cycling. The simulations also confirm that the current conceptual paradigm of sapropel formation and oxidation is valid and quantitatively coherent. 相似文献