地质成因的甲烷释放对大气的影响   总被引：2，自引：1，他引：2  

唐俊红  向武  鲍征宇  乔胜英  郭清宏 《地质科技情报》2006,25(2):75-82

地质成因自然源的甲烷释放在整个大气甲烷估算中起着非常重要的作用,它既是不含放射性14C甲烷源(死碳源)缺失部分的重要代表,也是甲烷重碳源的重要部分.概述了国内外关于地质成因甲烷释放对大气甲烷源与汇影响的研究进展,详述了来自地质成因化石燃料泄漏的人为甲烷释放以及来自沉积盆地(含油气盆地)、泥火山、地热区、海洋和甲烷水合物的地质自然源甲烷释放对大气甲烷源与汇的贡献及其影响因素;说明由于地质成因甲烷分布的区域性、不均匀性和时空的高度变化性,以及目前地质成因甲烷的通量估算仅建立在区域性的少量甲烷通量测试基础上,造成了地质成因甲烷释放通量估算的高度不确定性;指出研究中国西北地区油气田集聚区的甲烷释放通量,对油气田地质成因甲烷释放通量的估算具有重要意义.  相似文献   

天然气成因碳同位素指标评述     

孙秀凤  崔永强  邹胜权 《化工矿产地质》2006,28(4):225-233

地球排气过程和费-托合成反应中碳同位素分馏作用使其具有非常大的变化范围,覆盖了目前所说的有机成因气和无机成因气,要求人们重新审视目前判别无机成因气的碳同位素指标。天然气水合物中甲烷和二氧化碳较轻碳同位素值表明,无机成因天然气可以有更宽的同位素分布范围．碳同位素不是天然气成因唯一的判别方法,利用甲烷伴生气体的组分含量、天然气运移方式、赋存特征、与构造作用的关系都可以判断天然气的无机成因．  相似文献   

中国煤层气选区评价标准探讨   总被引：10，自引：0，他引：10  

王一兵田文广  李五忠赵庆波 田立志 《地质通报》2006,25(9):1104-1107

煤层气选区评价关系到勘探的成功与否,是煤层气勘探研究最基础的工作.近年国内外煤层气成藏理论、开发技术的快速发展,使得低煤阶气藏、连续薄层气藏、高煤阶低渗气藏等都获得成功开发,大大拓宽了煤层气的开发领域.此前国内在中煤阶成藏优势论基础上建立的选区标准已不适合当前的要求.根据当前存在的问题,结合煤层气成藏类型、地质特点和技术现状,对中国煤层气勘探选区评价标准进行了研究,试图建立一套煤层气选区评价标准,以期对国内煤层气选区评价工作提供借鉴.  相似文献   

Evaluating the coalbed methane potential of the Gething coals in NE British Columbia, Canada: An example from the Highhat area, Peace River coalfield     

Thomas Gentzis  David Schoderbek  Sharlene Pollock   《International Journal of Coal Geology》2006,68(3-4):135-150

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A study of ventilation transients associated with a controlled district recirculation circuit     

I. S. Lowndes 《Geotechnical and Geological Engineering》1987,5(4):353-368

Summary This paper discusses the development of a mathematical model to describe the unsteady airflow created and the subsequent effect on both the production and transportation of methane around the recirculation zone. Examples of the response of a single face recirculation system to various disturbances are presented and discussed.  相似文献   

Constraining anthropogenic CH4 emissions in Nanjing and the Yangtze River Delta,China, using atmospheric CO2 and CH4 mixing ratios     

SHEN Shuanghe  YANG Dong  XIAO Wei  LIU Shoudong  Xuhui LEE 《大气科学进展》2014,31(6):1343-1352

Methane （CH4） emissions estimated with the Intergovernmental Panel on Climate Change （IPCC） inventory method at the city and regional scale are subject to large uncertainties.In this study,we determined the CH4：CO2 emissions ratio for both Nanjing and the Yangtze River Delta （YRD）,using the atmospheric CH4 and CO2 concentrations measured at a suburban site in Nanjing in the winter.The atmospheric estimate of the CH4：CO2 emissions ratio was in reasonable agreement with that calculated using the IPCC method for the YRD （within 20％）,but was 200％ greater for the municipality of Nanjing.The most likely reason for the discrepancy is that emissions from unmanaged landfills are omitted from the official statistics on garbage production.  相似文献   

Bathymetric influence on dissolved methane in hydrothermal plumes revealed by concentration and stable carbon isotope measurements at newly discovered venting sites on the Central Indian Ridge (11–13°S)     

《Deep Sea Research Part I: Oceanographic Research Papers》2014

Methane is a useful tracer for studying hydrothermal discharge, especially where the source fluids are of low temperature and lack metal precipitates. However, the dual origins of deep-sea methane, both chemical and biological, complicate the interpretation of methane observations. Here, we use both the concentration and stable carbon isotopic composition (δ¹³C) of dissolved methane to trace hydrothermal plumes and identify the source and behavior of methane at two sites of newly discovered hydrothermal activity on the Central Indian Ridge (11–13°S). At both sites, methane and optical anomalies between 2500 and 3500 m at all stations indicate active hydrothermal discharge. We compared methane concentrations and δ¹³C at three stations, two (CTIR110136 and CTIR110208) with the most prominent anomalies at each site, and a third (CTIR110140) with near-background methane values. At stations CTIR110136 and CTIR110208, the concentration and δ¹³C of methane in distinct plumes ranged from 3.3 to 42.3 nmol kg⁻¹ and −30.0 to −15.4‰, respectively, compared to deep-water values of 0.5 to 1.2 nmol kg⁻¹ and −35.1 to −28.9‰ at the station with a near-background distal plume (CTIR110140). δ¹³C was highest in the center of the plumes at CTIR110136 (−15.4‰) and CTIR110208 (−17.8‰). From the plume values we estimate that the δ¹³C of methane in the hydrothermal fluids at these stations was approximately −19‰ and thus the methane was most likely derived from magmatic outgassing or the chemical synthesis of inorganic matter. We used the relationship between δ¹³C and methane concentration to examine the behavior of methane at the plume stations. In the CTIR110208 plume, simple physical mixing was likely the major process controlling the methane profile. In the CTIR110136 plume we interpret a more complicated relationship as resulting from microbial oxidation as well as physical mixing. We argue that this difference in methane behavior between the two areas stems from a distinct bathymetric dissimilarity between the two stations. The location of CTIR110208 on the open slope of a ridge allowed rapid plume dispersion and physical mixing, whereas the location of CTIR110136 in a small basin surrounded by wall structures inhibited physical mixing and enhanced microbial oxidation.  相似文献   

春、夏季长江口及邻近海域溶解甲烷的分布与释放通量     

孙明爽  张桂玲  王岚  叶旺旺  任景玲 《中国海洋大学学报(自然科学版)》2014,44(12):61-68

分别于2012年3和7月对长江口及其邻近海域进行了大面调查,测定了表、底层海水中溶解甲烷浓度,并对其海-气交换通量进行了估算。结果表明,春、夏季表层甲烷的平均浓度分别为(28.33±38.33)和(19.92±19.18)nmol·L-1,甲烷浓度从内河口向外海逐渐降低。长江口溶解甲烷浓度和饱和度有明显季节变化,其中春季内河口甲烷浓度和饱和度高于夏季,但外河口及邻近海域则相反,这主要是温度和长江冲淡水中甲烷浓度的季节差异造成的。该海域溶解甲烷的分布受陆源输入影响显著,夏季长江冲淡水影响范围较春季更广,但由于稀释效应夏季甲烷浓度低于春季。夏季沉积物的释放对河口区甲烷的贡献较春季更为明显。调查期间该海域溶解甲烷都处于过饱和状态,是大气甲烷的净源;根据W92公式初步估算出长江口及其邻近海区年释放CH4量约为8.81×108 mol·a-1,占全球海洋年释放量的0.08%,远高于其面积比0.01%,因此该海区是甲烷产生和释放的活跃海域。  相似文献   

南海F站位冷泉水体中的溶解甲烷     

张永  臧晚莹  杨庶 《海洋与湖沼》2022,53(3):590-596

目前对南海北部陆坡的F站位冷泉的研究多从地质和生物角度开展,而冷泉羽流在水平和垂直方向上的扩散范围尚不清晰,其影响因素尚不明确。针对该问题,于2021年6月6~23日搭乘“科学”轮对该冷泉海域的溶解甲烷进行调查,使用搭载遥控无人潜水器(Remote Operated Vehicle,ROV)和温盐深系统(Conductivity,Temperature,Depth,CTD)的采水瓶采集了该冷泉及邻近水体中从近海底(距底2.5 m)至表层(5~10 m)多个层位的水样,并使用气相色谱仪在现场分析了水样中溶解甲烷的含量。结果表明,溶解甲烷在覆盖喷口的生物繁茂区水体中的含量为6 590~11 300 nmol/L,在生物稀少的毗邻区迅速降至85.0~354.8 nmol/L。水柱剖面的测量结果显示冷泉喷口区1 000 m以深的水体中溶解甲烷含量高于背景区,而1 000 m以浅的水体中溶解甲烷的含量与背景区相同(2.01~3.90 nmol/L);自喷口区顺流向下1 500 m处,甲烷羽流信号消失。综上结果,甲烷羽流的水平扩散距离≤1 500 m,上升高度≤125 m。溶解甲烷的含量在生物繁茂区的迅速降低是由于底栖生物对溶解甲烷的摄食所致,而其在繁茂区之外扩散过程中的逐渐降低是海水湍流混合导致的稀释效应所致。  相似文献   

Methane adsorption comparison of different thermal maturity kerogens in shale gas system     

Haiyan Hu 《中国地球化学学报》2014,33(4):425-430

To determine the effect of thermal maturity on the methane sorption in shale gas system, two different thermal maturity kerogens of type II isolated from Barnett shale of Fort Worth Basin were used to measure the methane adsorption amount under the pressure ranging from 0 to 14 MPa at constant temperatures. One kerogen was called Lee C-5-1 with 0.58% of vitrinite reflectance; the other was called Blakely#1 kerogen with 2.01% of vitrinite reflectance. The results suggested that the methane sorption capacity of kerogen Blakely#1 was higher than the immature kerogen Lee C-5-1, and its Langmuir constant and Langmuir maximum sorption amount, which were reached by fitting the measured data for at least square method, greater than the immature kerogen Lee C-5-1. This may be associated with that nanopores opened up during the degradation of organic matter, and which increased the specific surface area of kerogen. Therefore, the over mature kerogen has greater methane adsorption capacity.  相似文献