西部中国沙棘叶片稳定碳同位素组成的空间特征及其气候意义   总被引：5，自引：3，他引：2  

刘光琇  张威  陈桂琛  章高森  李田  安黎哲 《中国沙漠》2009,29(5):866-871

分析了西部中国沙棘（Hippophate rhamnoides sinensis）叶片稳定碳同位素组成特征及其与环境因子之间的关系。结果表明,中国沙棘叶片δ13C值在-30.40‰~-24.91‰之间变化,平均值约为-27.62‰,属于C3植物。随纬度和经度的升高,中国沙棘叶片δ13C值明显升高,而随海拔的升高而降低,具有明显的空间分布特征。中国沙棘叶片δ13C值与温度没有明显的关系,随蒸发量和日照时间的升高而升高,随降水量的升高有降低趋势,具有明显的气候意义。表明中国沙棘具有较高的水分利用效率,水分是控制中国沙棘δ13C值变化或生长的主导因子。  相似文献   

Organic structure and possible origin of ancient charred paddies at Chuodun Site in southern China     

LinChao Hu  Xia Li  BenDing Liu  Min Gu  JingYu Dai 《中国科学D辑(英文版)》2009,52(1):93-100

A number of ancient charred paddies with a ¹⁴C dating of about 5900 a BP were recovered in the sixth excavation at Chuodun Site and are assigned to the Majiabang culture (7–6 ka BP). To understand their formation mechanism, the ancient charred paddies were compared to modern paddies using FT-IR spectrum and thermaogravimetric analysis. At the same time, modern charred paddies were made in helium by the laboratory method, and the structural characteristics of them and the ancient ones were revealed using CP/MAS-¹³C-NMR. Our results show there are more aromatic moieties in ancient charred paddies compared to modern paddies. The aliphatic components of modern charred paddies decrease continuously, accompanied by the accumulation of aromatic components, when the duration and temperature of oxidation increase, and the structure buildings of modern charred paddies are more similar to ancient ones. Given the planting manner of paddies during Majiabang culture period, these ancient charred paddies might be a result of the original farming mode involving fire. Supported by the National Natural Science Foundation of China (Grant No. 40571088)  相似文献   

赣江上游河流水化学的影响因素及DIC 来源   总被引：20，自引：0，他引：20  

李甜甜  季宏兵  江用彬  王丽新 《地理学报》2007,62(7):764-775

对赣江上游38 处水体采样点的水化学特征和溶解无机碳稳定同位素的分析, 发现其总溶解质浓度较低, 其中, 阳离子以Na⁺、Ca²⁺ 为主, 阴离子以Cl^- 和HCO₃ ^- 为主, Si 的浓度较高, 表征了典型硅酸盐地区河流的水化学组成特征。通过海盐校正分析得出, 研究区大气降水对河水溶解质的贡献率为11.5%, 扣除降水的贡献部分, 利用主成分分析的方法, 计算得出赣南流域受硅酸盐岩风化作用强烈, 同时由于受附近盐矿的影响, 蒸发盐岩的风化作用显著。另外, 根据δ¹³C 溶解无机碳DIC 的测量值约为-8.35‰~-13.74‰, 平均为-11.65‰, 利用质量平衡计算得出, 研究区DIC 的主要来源, 约68.5%来自于土壤CO₂, 31.5%来自于碳酸盐矿物的溶解, 进而得出流域岩石化学风化过程消耗的土壤CO₂ 为2.11×105 mol/yr·km², 来自碳酸盐本身的HCO₃ ^-含量为9.6×104 mol/yr·km²。由于地理位置和流域环境以及人为因素的差异, 各支流DIC 来源的比例亦有所差异。  相似文献   

荒漠植物叶片碳同位素组成及其水分利用效率   总被引：46，自引：17，他引：29  

陈拓  冯虎元  徐世建  强维亚  安黎哲 《中国沙漠》2002,22(3):288-291

水分通常是影响荒漠植物生长的主要限制因子,然而当前很少有关于荒漠群落中植物水分利用效率的报道。作为指示水分利用效率的可靠指标,叶片稳定碳同位素组成(δ¹³ C值)可以用来探讨植物适应干旱环境的强弱程度。对阜康和金塔同种或同属的植物叶片δ¹³ C的测量结果表明,干旱可使植物叶片δ¹³ C升高:年降水量每增加1mm,叶片δ¹³ C则降低001‰~ 0015‰。阜康荒漠灌木叶片δ¹³ C值明显高于草本,这样的趋势也存在于甘肃金塔主要荒漠植物中,与前人的报道也基本一致。说明灌木可能更适应干旱胁迫,并且这种现象可能是全球荒漠生态系统的一种共性。对阜康四种荒漠代表植物红砂、梭梭、补血草和骆驼刺的SOD活性的测定结果间接地支持了这一结果。进一步的分析表明,藜科、豆科和某些禾本科植物适应干旱环境的能力相对较强。  相似文献   

A wavelet method for detecting S‐waves in seismic data     

P.J. Oonincx 《Computational Geosciences》1999,3(2):111-134

Seismic signals consist of several typically short energy bursts, called phases, exhibiting several patterns in terms of dominant frequency, amplitude and polarisation. We present a fast algorithm to detect the so‐called S‐phase in a three‐component seismic signal. This new approach combines traditional S‐phase detection methods and the discrete wavelet transform. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

¹³C示踪技术在利玛原甲藻中腹泻性贝毒合成研究的应用          下载免费PDF全文

张昊宇  谭志军  郑关超  吕颂辉  杨越聪  吴海燕 《海洋与湖沼》2023,54(2):457-464

选取具有显著产毒差异的利玛原甲藻(Prorocentrum lima) SHG株与2XS株为研究对象,以2-¹³C-甘氨酸为示踪原料结合高分辨质谱方法,为腹泻性贝类毒素及其酯化态毒素合成与代谢途径的研究提供新方法和思路。结果表明,两株藻共发现16种腹泻性贝毒及其酯化态毒素成分。对照培养条件下SHG株(大田软海绵酸毒素含量为7.88 pg/cell,鳍藻毒素1含量为4.35 pg/cell)的产毒能力高于2XS株(大田软海绵酸毒素5.70pg/cell),而甘氨酸作为氮源培养条件可显著提高两株藻的产毒总量(P<0.05)。¹³C-甘氨酸标记组与甘氨酸培养组单细胞产毒量无显著变化(P>0.05)。腹泻性贝毒被标记后其同位素异构体丰度发生变化,其中酯化态受¹³C标记的影响程度更高,二级质谱图清晰表示出其碎片离子及脱水峰的标记情况。该方法直观阐明了甘氨酸可作为P. lima标记原料的产毒供体,并使用稳定同位素标记方法首次实现了酯化态的同步标记,有助于腹泻性贝毒生成机制的进一步研究。  相似文献   

Spectroscopic Characterization of Organic Structures and Organic‐Inorganic Interactions in Paper Mill Sludge     

Claudia M. B. F. Maia  Fabio Simonelli  Antinio S. Mangrich 《洁净——土壤、空气、水》2001,28(7):372-377

The organic composition and organic‐inorganic interaction in paper mill sludge (PS) solvent extracts (hexane, ethyl acetate, acetone and ethanol) and humic fractions, humic acid (HA) and humin (HU) were studied by electron paramagnetic resonance spectroscopy (EPR), proton and carbon‐13 nuclear magnetic resonance spectroscopy (¹H NMR; ¹³C NMR), Fourier‐transformed infrared spectroscopy (FTIR), and ultraviolet‐visible spectroscopy (UV‐vis). The strategy of fractionating the PS, sequentially, with organic solvents of increasing polarity is a reliable analytical procedure for humic substance sample separation because it results in more purified fractions. FTIR, ¹H NMR and ¹³C NMR results showed that hexane extract consisted mainly of aliphatic hydrocarbon structures. Their contents in the extracts decreased as the polarity of the extracting solvent increased and the content of oxygen functional groups increased. Carboxylic and carboxylate functional groups were found in the acetone extract, and ester and ether functions were predominantly found in the ethanol extract. EPR spectra revealed some Fe³⁺ complexes with rhombic structure (g₁ = 4.3; g₂ = 9.0) in the humic fractions and in all solvent extracts, except hexane. Quasi‐octahedral Fe³⁺ complexes (g = 2.3; ΔH_pp ≤ 400 G) were found in the HU fraction and in the acetone extract. The organic free radical content in the HA fraction was higher than the non‐fractionated PS sample and HU fraction.  相似文献   

Stable carbon isotope variations in northwest Europe during the last glacial–interglacial transition     

Chris S. M. Turney  David J. Beerling  Douglas D. Harkness  J. John Lowe  E. Marian Scott 《第四纪科学杂志》1997,12(4):339-344

Stable carbon isotope data that span part of the last glacial–interglacial transition (ca. 14-9 ka ¹⁴C BP; ca. 15–11 ka cal. BP), and which derive from organ-specific plant macrofossils recovered from two lake sediment profiles in the UK and one in Norway, are compared. The recorded temporal variations show similar trends, which, over a millennial time-scale appear to parallel the main drift in δ¹⁸O as determined for the GRIP ice-core. It is postulated that some smaller scale variations in the δ¹³C profiles may reflect the shorter term oscillations in δ¹⁸O values evident in the GRIP record, although this is less certain. Overall, however, the results suggest that stable carbon isotope measurements based on organ-specific terrestrial plant macrofossils may provide (i) a means for establishing correlations between terrestrial successions and (ii) additional paleoenvironmental information, as the apparent ‘shadowing’ of the GRIP record indicates a common forcing mechanism for both Greenland δ¹⁸O and northwest European δ¹³C variations. From the evidence available we suggest that the recorded δ¹³C variations reflect fluctuations in air temperature and/or changes in water vapour pressure in the atmosphere. © 1997 John Wiley & Sons, Ltd.  相似文献   

利用浮石合成13X型分子筛最佳工艺条件的研究     

金为群  权新军  蒋引珊  张军 《吉林大学学报(地球科学版)》1997,(2)

以吉林省长白山地区的天然浮石为原料，成功地合成了１３Ｘ型分子筛，对其合成路线，反应条件进行了研究，确定了合成１３Ｘ型分子筛的最佳工艺条件，并通过Ｘ射线衍射法及差热分析等手段证明了产物的结构  相似文献   

Chemical structural models for coalified wood (vitrinite) in low rank coal     

Patrick G. Hatcher 《Organic Geochemistry》1990,16(4-6)

Examination of a series of coalified gymnospermous woods ranging in rank from brown coal to subbituminous coal by solid-state ¹³C NMR and analytical pyrolysis has provided sufficient information to construct structural models depicting the changes that occur to lignin, the primary precursor of vitrinite, during coalification. Progressive changes in the chemistry of coalified wood suggest the following series of reactions: (1) demethylation to form catechol-like structures that are dominant components of brown coal and lignite A; (2) cleavage of aryl ether linkages to form phenols and reactive carbocations that alkylate the catechol rings; (3) dehydration of the catechol rings; (3) dehydration of the catechol-like structures to form the structures of subbituminous coal dominated by alkylphenols; and (4) reduction of the 3-carbon alkyl side chain derived from lignin to form propyl substituents. The models developed for each stage of coalification are derived from chemical modifications of the structure of lignin.  相似文献