基于能源消费的中国不同产业空间的碳足迹分析

Using energy consumption and land use data of each region of China in 2007,this paper established carbon emission and carbon footprint model based on energy consumption,and estimated the carbon emission amount of fossil energy and rural biomass energy of dif-ferent regions of China in 2007.Through matching the energy consumption items with indus-trial spaces,this paper divided industrial spaces into five types:agricultural space,living & industrial-commercial space,transportation industrial space,fishery and water conservancy space,and other industrial space.Then the author analyzed the carbon emission intensity and carbon footprint of each industrial space.Finally,advices of decreasing industrial carbon footprint and optimizing industrial space pattern were put forward.The main conclusions are as following:(1) Total amount of carbon emission from energy consumption of China in 2007 was about 1.65 GtC,in which the proportion of carbon emission from fossil energy was 89%.(2) Carbon emission intensity of industrial space of China in 2007 was 1.98 t/hm2,in which,carbon emission intensity of living & industrial-commercial space and of transportation in-dustrial space was 55.16 t/hm2 and 49.65 t/hm2 respectively,they were high-carbon-emission industrial spaces among others.(3) Carbon footprint caused by industrial activities of China in 2007 was 522.34 106 hm2,which brought about ecological deficit of 28.69 106 hm2,which means that the productive lands were not sufficient to compensate for carbon footprint of industrial activities,and the compensating rate was 94.5%.As to the regional carbon footprint,several regions have ecological profit while others have not.In general,the present ecologi-cal deficit caused by industrial activities was small in 2007.(4) Per unit area carbon footprint of industrial space in China was about 0.63 hm2/hm2 in 2007,in which that of living & indus-trial-commercial space was the highest (17.5 hm2/hm2).The per unit area carbon footprint of different industrial spaces all presented a declining trend from east to west of China.     

The carbon cycle and biogeochemical dynamics in lake sediments

The concentrations of organic carbon (OC) and CaCO3 in lake sediments are often inversely related. This relation occurs in surface sediments from different locations in the same lake, surface sediments from different lakes, and with depth in Holocene sediments. Where data on accumulation rates are available, the relation holds for organic carbon and CaCO3 accumulation rates as well. An increase of several percent OC is accompanied by a decrease of several tens of percent CaCO3 indicating that the inverse relation is not due to simple dilution of one component by another. It appears from core data that once the OC concentration in the sediments becomes greater than about 12%, the CO2 produced by decomposition of that OC and production of organic acids lowers the pH of anoxic pore waters enough to dissolve any CaCO3 that reaches the sediment-water interface. In a lake with a seasonally anoxic hypolimnion, processes in the water column also can produce an inverse relation between OC and CaCO3 over time. If productivity of the lake increases, the rain rate of OC from the epilimnion increases. Biogenic removal of CO2 and accompanying increase in pH also may increase the production of CaCO3. However, the decomposition of organic matter in the hypolimnion will decrease the pH of the hypolimnion causing greater dissolution of CaCO3 and therefore a decrease in the rain rate of CaCO3 to the sediment-water interface.     

喜马拉雅珠峰地区冬季大气气溶胶化学组分及光学特征

为了研究喜马拉雅山北坡冬季大气气溶胶化学组分、光学特征及来源,2017年11—12月在珠穆朗玛峰站(QOMS)共采集22个PM2.5样品.结果显示:PM2.5中包括水溶性离子(WSIs)、有机质(OM)、元素碳(EC)在内的所有检测成分,总质量浓度为(3.36±1.06)μg·m-3;有机碳(OC)、元素碳(EC)和水...     

多巴胺在聚3，4-吡啶二羧酸修饰电极上的电化学行为及其测定

制备了聚3,4-吡啶二羧酸修饰电极,研究了多巴胺在修饰电极上的电化学行为。结果表明聚3,4-吡啶二羧酸聚合物膜对多巴胺的氧化具有明显的催化作用,并且可以消除抗坏血酸对多巴胺测定中的干扰。多巴胺的浓度在2.0×10-6～4.0×10-5mol/L内与其氧化电流呈线性关系,相对标准偏差为3.2%(n=10),检出限为8.0×10-8mol/L。将该修饰电极用于分析模拟样品和注射液样品中的多巴胺,分析结果表明,该修饰电极有望用于实际样品分析。     

硫酸参与的长江流域岩石化学风化速率与大气CO2消耗

流域的岩石化学风化过程是全球碳循环中的重要环节。以往的流域水化学碳汇通量估算大多是基于碳酸的风化作用。而实际上,硫酸和碳酸一样,也参与了流域碳元素的地球化学循环,从而对全球碳循环过程产生影响。长江流域水体近几年出现酸化现象,大部分河段SO42-和Ca2+含量增高,其对应的岩石风化过程和大气CO2消耗速率也发生变化。文章对长江干流及主要支流2013年不同季节的离子组成进行监测,利用水化学平衡法和Galy估算模型,对长江流域岩石化学风化速率和CO2消耗通量进行了估算,对硫酸参与下的长江流域岩石风化和碳循环过程进行了分析。结果表明,长江流域水体离子主要来源于硅酸盐岩风化和碳酸盐岩风化。其中碳酸盐岩风化对河水离子贡献率为92%。在硅酸盐岩广泛分布的赣江流域,碳酸盐岩风化离子贡献也达85%。分析表明,硫酸参与了长江流域的岩石风化过程,对水体中离子产生一定影响。硫酸的参与加快了碳酸盐岩的化学风化速率,平均提高约30%,但是使流域大气CO2消耗速率降低。在不考虑蒸发岩溶蚀作用下,平均从516×103 mol/km2·a降至356×103 mol/km2·a,降低约31%。在各支流中,硫酸对乌江流域碳酸盐岩的风化和碳循环的影响最大,而对雅砻江的影响最小,这与乌江流域的含煤地层、矿床硫化物及大气酸沉降有关。     

西藏搭格架地热区天然水的水化学组成与稳定碳同位素特征

为探究青藏高原搭格架地热区地热水、湖水、河水、冰雪融水等天然水体的水化学组成及物质来源控制因子,于2014年8月对该地区进行了考察和取样。利用紫外-可见光分光光度计和ICP-OES测定了水样中各阴、阳离子含量,利用Gas Bench连接同位素质谱仪测定了水样中溶解无机碳（DIC）同位素比值。结果表明,地热水中总溶解固体（TDS）含量为977.13~1 279.50 mg/L,阳离子以K+和Na+为主,阴离子以HCO3-和Cl-为主,湖水的TDS含量为77.81~810.94 mg/L,阳离子以Na+和Ca2+为主,阴离子以HCO3-(CO32-)和SO42-为主,地热水和湖水的水化学类型为HCO3-Na型;河水和冰雪融水的各离子含量较低,水化学类型为HCO3-Ca型;地热水的DIC浓度范围为9.2~15.4 mmol/L,δ13CDIC值为-9.09‰~-0.95‰;湖水的DIC浓度为1.1~9.7 mmol/L,δ13CDIC值为-8.84‰~-0.27‰。根据水化学Gibbs分布模式图判断出区域水化学特征主要受硅酸盐岩风化控制,以钠长石和钾长石风化为主,但是地热水的水化学组分受到硅酸盐岩和蒸发盐岩共同控制。通过碳同位素比值分析对区域主要风化过程中CO2的来源示踪表明,湖区周围的硅酸盐风化其碳源主要为土壤CO2,热泉区硅酸盐水解其碳源为地球深部CO2输入。      

河北坝上高原小滦河流域古土壤碳库地质成因和稳定性评价

土壤碳库是陆地生态系统中最大的碳库，以往研究主要针对现代土壤碳库，而古土壤的碳库特征研究相对薄弱。本文以河北坝上高原小滦河流域古土壤为研究对象，通过光释光（OSL）年代学、元素地球化学、团聚体分析方法，研究了风成沙地稀疏草地单元和河湖残积灌草混合单元内古土壤碳库特征。结果表明：古土壤形成时代为5. 7~3. 3 ka的全新世温暖期，气候温暖湿润，雨水充足，发育以松和蒿属为主要建群种的针叶林－草原植被。碳库以有机碳（SOC）为主，平均有机碳密度为3. 85 kg/m2，有机碳库储量为153. 1×107 kg。河湖相沉积物微团聚体的含量较高，对古土壤层碳库的物理保护作用较强，碳库稳定性较高；风积相沉积物微团聚体含量相对较低，加速有机碳的分解，碳库稳定性较差。提出不同沉积单元的土地利用保护方式，减少土壤有机碳的分解流失，支撑当地碳达峰、碳中和工作推进。     

土壤中总有机碳环境标准样品研制

土壤环境标准样品是土壤生态环境监测质量控制的重要技术工具.目前,土壤中总有机碳环境标准样品仍为中国环境标准样品体系的空缺,特别是配套燃烧氧化-非分散红外法的土壤标准样品一直未曾问世.本文以有机碳含量较高的农用地土壤为原材料,经干燥、研磨、混匀、装瓶、灭菌等加工步骤,制备获得土壤中总有机碳环境标准样品.分层随机抽取10瓶...     

河蚬壳体不同断面碳、氧同位素研究

生物壳体碳酸盐的稳定氧、碳同位素已经被广泛地应用在古气候、古环境研究中,在生物壳体就位分析中,壳体不同断面上同位素的差异将影响对壳体同位素所指示的环境意义的判断,从而对利用其提取气候环境信息造成不利影响。本文对河蚬壳体不同断面碳氧同位素进行了研究,结果表明:河蚬壳体碳同位素变化序列在不同断面上不存在显著差异,因此在做碳同位素时间序列研究时可以不考虑不同断面差异的问题,在取样过程中可以通过延长取样的长度来获得足够量的样品进行碳同位素的测定;而氧同位素变化序列在不同断面上存在差异,因此在进行壳体就位分析研究时,选取不同断面上氧同位素变化序列对研究结果影响较大,存在壳体断面选择的问题,而在取样过程中取样的长度应控制在一定范围内,避免同一生长环上距离较远位置粉末的混合。文中最后根据壳体不同断面同位素差异确定了在壳体就位分析中如何选取研究断面。     

攀西宁南地区上震旦统灯影组麦地坪段C、O同位素特征和震旦系/寒武系界线的划分

对上震旦统灯影组麦地坪段的C、O同位素组成进行了分析,并根据δ13C值在剖面上的变化特征,讨论了该地区震旦系/寒武系的界线。结果表明,麦地坪段白云岩δ13C值在-3.19‰～2.86‰之间,平均值为0.10‰;δ18O值在-10.75‰～-5.17‰之间,平均值为-7.82‰。在剖面上δ13C值出现了有规律的变化,剖面下部2～21层,δ13C值均为正值,在0.04‰～1.68‰之间,平均值为0.92‰;上部23～32层,δ13C值均为负值,在-3.19‰～-1.42‰之间,平均值为-2.13‰,δ13C值存在一个显著的负漂移,变化高达4‰。麦地坪段白云岩δ13C值的变化特征与国内外同期地层非常相似,具有全球可对比性,可作为震旦系/寒武系划分的地球化学标志。