Heavy metal pollution in China: Origin, pattern and control

Goal, Scope and Background. Heavy metal is among one of the pollutants, which cause severe threats to humans and the environment in China. The aim of the present review is to make information on the source of heavy metal pollution, distribution of heavy metals in the environment, and measures of pollution control accessible internationally, which are mostly published in Chinese. Methods. Information from scientific journals, university journals and governmental releases are compiled focusing mainly on Cd, Cu, Pb and Zn. Partly Al, As, Cr, Fe, Hg, Mn and Ni are included also in part as well. Results and Discussion. In soil, the average contents of Cd, Cu, Pb and Zn are 0.097, 22.6, 26.0 and 74.2 mg/kg, respectively. In the water of. the Yangtze River Basin, the concentrations of Cd, Cu, Pb and Zn are 0.080, 7.91, 15.7 and 18.7 pg/L, respectively. In reference to human activities, the heavy metal pollution comes from three sources: industrial emission, wastewater and solid waste. The environment such as soil, water and air were polluted by heavy metals in some cases. The contents of Cd, Cu, Pb and Zn even reach 3.16, 99.3, 84.1 and 147 mg/kg, respectively, in the soils of a wastewater irrigation zone. These contaminants pollute drinking water and food, and threaten human health. Some diseases resulting from pollution of geological and environmental origin, were observed with long-term and non-reversible effects. Conclusions. In China, the geological background level of heavy metal is low, but with the activity of humans, soil, water, air, and plants are polluted by heavy metals in some cases and even affect human health through the food chain. Recommendations and Outlook. To remediate and improve environmental quality is a long strategy for the polluted area to keep humans and animals healthy. Phytoremediation would be an effective technique to remediate the heavy metal pollutions.

Fracture properties of silicon carbide thin films by bulge test of long rectangular membrane

This paper reports the mechanical properties and fracture behavior of silicon carbide (3C-SiC) thin films grown on silicon substrates. Using bulge testing combined with a refined load-deflection model of long rectangular membranes, which takes into account the bending stiffness and prestress of the membrane material, the Young's modulus, prestress, and fracture strength for the 3C-SiC thin films with thicknesses of 0.40 and 1.42 mu m were extracted. The stress distribution in the membranes under a load was calculated analytically. The prestresses for the two films were 322 +/- 47 and 201 +/- 34 MPa, respectively. The thinner 3C-SiC film with a strong (111) orientation has a plane-gstrain moduli of 415 +/- 61 GPa, whereas the thicker film with a mixture of both (111) and (110) orientations exhibited a plane-strain moduli of 329 +/- 49 GPa. The corresponding fracture strengths for the two kinds of SiC films were 6.49 +/- 0.88 and 3.16 +/- 0.38 GPa, respectively. The reference stresses were computed by integrating the local stress of the membrane at the fracture over edge, surface, and volume of the specimens and were fitted with Weibull distribution function. For the 0.40-mu m-thick membranes, the surface integration has a better agreement between the data and the model, implying that the surface flaws are the dominant fracture origin. For the 1.42-mu m-thick membranes, the surface integration presented only a slightly better fitting quality than the other two, and therefore, it is difficult to rule out unambiguously the effects of the volume and edge flaws.

Design of spectrometer based on volume phase grating for near infrared range

In order to design and fabricate a spectrometer for the infrared range widely used in the different applications, Volume Phase Grating (VPG) with. low Polarization Dependence Loss (PDL) and high efficiency has been adopted as the dispersion element. VPG is constructed by coating an optical substrate with a thin film of dichromated. gelatin and exposing the film to two mutually coherent laser beams to form index modulation. The diffraction efficiency for a VPG is governed by Bragg effects. The depth (d) and index modulation contrast of the grating structure control the efficiency at which the light is diffracted when the Bragg condition is satisfied. Gradient index lens with high performance and low aberration are used as collimating system instead of standard lens. The spot diagrams and MTF curve of the collimating lens are shown in the paper. The receive system is InCaAs photodiode (PD) array including 512 pixels with 25 mum pitch. The spectrum resolution of the spectrometer reaches to 0.2nm and wavelength accuracy is 40pm.

Tolerance analysis for incident angle of volume phase holographic grating used in optical channel performance monitor

Transmission Volume Phase Holographic Grating (VPHG) is adopted as spectral element in the real-time Optical Channel Performance Monitor (OCPM), which is in dire need in the Dense Wavelength -division-multiplexing(DATDM) system. And the tolerance of incident angle, which can be fully determined by two angles: 6 and (p, is finally inferred in this paper. Commonly, the default setting is that the incident plane is perpendicular to the fringes when the incident angle is mentioned. Now the situation out of the vertical is discussed. By combining the theoretic analysis of VPHG with its use in OCPM and changing 6 and (0 precisely in the computation and experiment, the two physical quantities which can fully specify the performance of VPHG the diffraction efficiency and the resolution, are analyzed. The results show that the diffraction efficiency varies greatly with the change of 6 or (p. But from the view of the whole C-band, only the peak diffraction efficiency drifts to another wavelength. As for the resolution, it deteriorates more rapidly than diffraction efficiency with the change of (p, while more slowly with the change of theta. Only if \phi\less than or equal to+/-1degrees and alpha(B) -0.5 less than or equal to theta less than or equal to alpha(B) + 0.5, the performance of the VPHG would be good enough to be used in OCPM system.

杉木人工林凋落物对土壤碳平衡的影响

土壤碳循环过程是目前全球碳源碳汇研究的核心，目前对土壤碳循环过程和机制的研究还十分缺乏。杉木人工林约占我国人工林面积的1/4，由于近几十年经营管理措施不当，土壤有机碳的下降已经成为不争的事实，极大地影响了杉木人工林生产力的可持续发展。本研究通过对杉木人工林土壤有机碳来源、分解和释放动态的区分量化，结合13C标记示踪试验，开展了杉木凋落物分解对土壤有机碳平衡影响的研究，为土壤碳平衡和转化机理及杉木人工林的可持续经营提供了可靠的理论依据。通过系统的研究，得出以下结论： ⑴估算了典型杉木人工林土壤碳的周转状况，研究发现典型杉木人工林土壤碳更新较慢。土壤碳年输入量、形成量、转化量、输出量和贮存量分别为2.79 t hm-2、1.58 t hm-2、2.04 t hm-2、4.57 t hm-2、113.21 t hm-2。其中在土壤碳年排放量中矿质土层呼吸、根呼吸、凋落物层呼吸碳分别占土壤碳总排放量的50.6%、26.0%、23.1%。 ⑵计算了凋落物分解对土壤碳平衡的贡献。不同器官凋落物在土壤中的矿化释放碳量和进入土壤碳库量均随着凋落物易分解性的增大而增大，并且各器官凋落物分解以CO2-C释放最多，以微生物量碳存在的量次之，以可溶性碳存在的量最少。年均温16.5 ℃条件下培养100天，分别来自于叶、枝、细根、粗根有机碳的13.81%、9.26%、5.74%、4.62%被矿化释放，占总CO2-C释放量的比例分别为43.7%、37.2%、31.9%、29.0%。同时不同器官凋落物依次有3.05%、3.26%、2.24%、1.84%存在于土壤微生物碳库，占总微生物量碳的比例分别为12.9%、14.3%、10.5%、8.8%；不同器官凋落物依次有0.62%、0.62%、0.31%、0.24%存在于可溶性有机碳库，占总可溶性有机碳的比例分别为3.99%、4.10%、2.13%、1.73%。 ⑶不同器官凋落物进入土壤对土壤碳排放的激发效应不同，叶、枝、细根、粗根加入土壤产生了正激发效应，激发率依次为6.6%、7.0%、2.2%、2.8%。并且土壤风干－湿润过程影响了凋落物在土壤中的分解和转化过程。土壤风干－湿润使起始矿化底物库增大，培养初期凋落物分解速率上升，同时土壤原有机碳矿化速率降低，微生物对凋落物碳的利用以及凋落物对可溶性有机碳的贡献下降。 ⑷凋落物碳在不同轻组密度组分中的分布不同，但各器官凋落物间无明显差异，均为中等密度自由轻组最多，其次为最小密度自由轻组，最少为闭蓄轻组。室外培养224天，结果表明叶、枝、细根、粗根凋落物在各密度组分中的分配情况为：<1.0 g cm-3自由轻组中16.5~19.1%，1.0~1.8 g cm-3自由轻组中56.8~65.2%，闭蓄轻组中残留5.7~6.9%，其余的9.9～21.0%被矿化损失。研究还表明，凋落物粉碎添加方式能改变其在土壤组分中的分布比例，倾向于向较重的密度组分中分布而被保护起来利于有机碳的积累。

禄春安息香种子和攀援孔药花全草的化学成分研究

本文对禄春安息香（Styrax macranthus）种子和攀援孔药花（Porandra scandens）全草的化学成分进行了研究，共获得30个化合物，其中2个为新化合物。 从禄春安息香种子95%乙醇提取物中分离并鉴定了12个化合物，其中2个新化合物鉴定为3-[7-methoxy-2-(3,4-methylenedioxy phenyl) benzofuran-5-yl] propyl 3-[7-methoxy-2-(3,4-methylenedioxyphenyl)benzofuran-5-yl] propanoate (1) 和去甲氧基-egonol-龙胆双糖甙 (2)；已知化合物分别为2-(3,4-二氧亚甲基苯基)-5-甲酰基-7-甲氧基-苯并呋喃 (3)、egonol (4)、去甲氧基-egonol (5)、去甲基-egonol (6)、egonol-葡萄糖甙 (7)、egonol-龙胆双糖甙 (8)、egonol-龙胆三糖甙 (9)、豆甾醇 (10)、二十四烷酸 1-甘油酯 (11) 和胡萝卜甙 (12)。生物活性测试发现，化合物2具有促进雌激素E2合成的作用。 从攀援孔药花全草95%乙醇提取物中分离并鉴定了19个化合物：(2S,3S,4R)-2-[(2R)-2-羟基-二十一烷酰基氨基]-二十一烷-1,3,4-三醇 (13)、(2S,3S,4R)–2–二十四烷酰基氨基-十八烷-1,3,4-三醇 (14)、胡萝卜甙 (12)、β-谷甾醇 (15)、(20S,22E,24R)-5α,8α-表二氧-麦角甾-6,22-二烯-3β-醇 (16)、6β-羟基-豆甾-4-烯-3-酮 (17)、十六烷酸 1-甘油酯 (18)、桦木酸 (19)、大黄素 (20)、二十二烷酸 1-甘油酯 (21)、对羟基苯甲醛 (22)、十七烷酸 1-甘油酯 (23)、金色酰胺醇乙酸酯(24)、十九烷酸 1-甘油酯 (25)、棕榈酸 (26)、(E)-p-香豆酸 (27)、(22E,24S)-24-麦角甾醇-7,22-二烯-3β,5α,6β-三醇 (28)、2-去氧-β-蜕皮激素 (29)和auranamide (30)。 综述了近十年来发现的2－芳基苯并呋喃类新木脂素的结构特征、来源、生物活性和化学全合成。 Phytochemical investigation on the seeds of Styrax macranthus and the whole plants of Porandra scandens led to the isolation of thirty compounds, two of which were new ones. Two new 2-aryl benzofuran derivatives, 3-[7-methoxy-2-(3,4-methylenedioxy phenyl) benzofuran-5-yl]propyl 3-[7-methoxy-2-(3,4-methylenedioxyphenyl)benzo furan-5-yl]propanoate (1) and demethoxy egonol gentiobioside (2), were isolated from the 95% aqueous ethanolic extract of the seeds of Styrax macranthus, together with 7-methoxy-2-(3,4-methylenedioxyphenyl) benzofuran-5-carbaldehyde (3), egonol (4), demethoxy egonol (5), demethyl egonol (6), egonol glucoside (7), egonol gentiobioside (8), egonol gentiotrioside (9), stigmasterol (10), 2,3-dihydroxypropyl tetracosoate (11), and daucosterol (12). In vitro test, compound 2 promote the synthesis of estrogen E2. Nineteen compounds were isolated from the 95% aqueous ethanolic extract of the whole plant of Porandra scandens for the first time. Their structures were identified as (2S,3S,4R)-2-[(2R)-2-hydroxy-heneicosanoylamino]-1,3,4- heneicosanetriol (13), (2S,3S,4R)-2-tetracosanoylamino-1,3,4-octadecanetriol (14), daucosterol (15), β-sitosterol (12), (20S,22E,24R)-5α,8α-epidioxy-ergosta-6,22-diene- 3β-ol (16), 6β-hydroxylstigmast-4-en-3-one (17), 1-glycerol-1-hexadecoate (18), betulinic acid (19), emodin (20), 1-glycerol-1-docosoate (21), p-hydroxybenzaldehyde (22), 1-glycerol-1-heptadecoate (23), aurantiamide acetate (24), 1-glycerol-1- nonadecoate (25), palmatic acid (26), (E)-p-coumaric acid (27), (22E,24S)- 24-metbylcbolesta-7,22-diene-3β,5α,6β-triol (28), 2-deoxycrustecdysone (29), and auranamide (30). The characteristic, natural resource, bioactivity, and the total synthesis of 2-aryl benzofurans were reviewed.

唐古特瑞香和大果大戟的化学成分研究

本学位论文由两部分共3章组成。第一部分分别报道2种藏药唐古特瑞香和大果大戟化学成分的研究成果，从2种药用植物共分离鉴定了60个不同的化合物，其中12个为新结构，特别有意义的是发现了2个具有同一新骨架的二萜化合物。第二部分概述了大戟科植物多环二萜的研究进展。 第一部分包括第1和2章。在这2章中分别报道了唐古特瑞香（Daphne tangutica Maxim）和大果大戟（Euphorbia wallichii Hook. f. Fl）化学成分的分离纯化与结构鉴定。实验采用正、反相硅胶柱层析、薄层制备及HPLC等分离方法，从唐古特瑞香的根皮中共分离出32个化合物，通过红外、质谱及核磁共振等波谱方法鉴定了其中的31个，结构类型分别属于瑞香二萜类、木脂素类、香豆素类、苯丙素类及甾体类，其中有三个新的瑞香二萜型化合物，经波谱分析将它们的结构分别鉴定为1,2a-二氢-20-棕榈酰瑞香毒素、1,2a-二氢-5b-羟基-6a,7a-环氧-树脂大戟醇-14-苯甲酸酯及1,2b-二氢-5b-羟基-6a,7a-环氧-树脂大戟醇-14-苯甲酸酯，另外还有13个已知化合物为首次从该植物中分离得到。从大果大戟的根部共分离出33个化合物，鉴定了其中的30个，其主要成分为种类丰富的二萜，包括巨大戟烷型、续随子烷型、对映－阿替生烷型、对映－贝壳杉烷型、对映－松香烷型、ent-trachylobane型、对映－异海松烷型及一新骨架五环二萜ent-wallichane型，另外还有香豆素、甾体、三萜和一些简单的小分子化合物。其中新化合物有9个，经波谱分析将它们的结构分别鉴定为5-O-(2E,4E,6E)-癸三烯酰基-3,20-O-二乙酰基巨大戟醇、5-O-(2E,4Z)-癸二烯酰基-3-O-乙酰基-20-去氧巨大戟醇、3-O-(2E,4Z)-癸二烯酰基-5b,6b-氧-交京大戟醇、7-苯甲酰氧基-3,5,15-三乙酰基-续随子醇、ent-trachylobane-3-one-17-oic-acid、3α-羟基-对映-阿替斯-16-烯-14-酮、3α,6-二羟基-对映-异海松-7-烯-2,15-二酮、wallichanol A 和 wallichanol B，其中，wallichanol A 和 wallichanol B属于一新骨架类型的五环二萜。除此以外，另有13个已知化合物为首次从该植物中分离得到。 第2部分即第3章，首次概述了大戟属植物中多环二萜的化学和药理研究进展。 This dissertation is composed by two parts. The first part reports the phytochemical investigation of two Tibetan medicine plants, Daphne tangutica Maxim and Euphorbia wallichii Hook. f. Fl. Sixty different compounds including ten new compounds and two novel diterpenoids possessing a new carbon skeleton were isolated and identified. The second part is a review about the progress of studies on the polycyclic diterpeniods of the plant family of Euphorbia. The first part consists two chapters, which expatiate on the isolation and identification of chemical constituents from D. tangutica and E. wallichii. Thirty-one compounds were isolated from the root barks of D. tangutica by methods of column chromatography (silica gel, including reversed phase), preparative TLC and HPLC, and their structure were identified as nine daphnane diterpenes, six lignans, nine cumarin derivatives, five phenylpropanoid derivatives, a steroids and a benzoate on the basis of spectroscopic methods including IR, MS and NMR. Among them, three are new diterpenes with skeleton of daphnane and the structure were determined as 1,a-dihydro-20-palimoyl-daphnetoxin, 1,2a-dihydro-5b- hydroxy-6a,7a-epoxy-resiniferonol-14-benzoate and 1,2b-dihydro-5b-hydroxy- 6a,7a-epoxy-resiniferonol-14-benzoate. In addition, thirteen known ones were isolated from this plant for the first time. Isolation of the roots of E. wallichii yielded thirty compounds, twenty-four of them were elucidated as diterpenoids, which belong to different skeleton types of ingenol, lathyrane, ent-atisane, ent-kaurane, ent-abietane, ent-trachylobane, ent-isopimarane and a new pentacyclic skeleton ent-wallichane respectively. The remains including a cumarine, a triterpenoid, a steroid and three compounds with small molecule. Nine new compounds were characterized as 5-O-deca-2E,4E,6E- trienoyl-3,20-O-diacetylingenol, 5-O-deca-2E,4Z-dienoyl-3-O-acetyl-20- deoxyingenol, 3-O-deca-2E,4Z-dienoyl-jolkinol-5b,6b-oxide, 7-benzoyl-3,5,15- triacetyl-7-hydroxylathyrol, ent-trachylobane-3-one-17-oic-acid, 3α-hydroxy-ent- atis-16-en-14-one, 3α,6-dihydroxy-ent-isopimarane-7-en-2,15-dione, wallichanol A and wallichanol B, respectively, by means of comprehensive spectroscopic analysis. Among them, wallichanol A and wallichanol B were two notable novel pentacyclic diterpenoids processing a new rearranged carbon skeleton. And more, thirteen ones were firstly reported from this plant. The third chapter summarizes the research development on chemistry and pharmacology of polycyclic diterpenes from the plant family of Euphorbia for the first time.

中药射干的化学成分研究

本学位论文由4章组成。第一章是论文的主体，报道了中药射干的化学成分研究。第二章是中药射干代用品川射干的化学成分研究，并附带报道了西番莲化学成分的研究结果。第三章是射干、川射干及西番莲提取物化学成分串联质谱分析的报道。第四章为综述，概述了射干及鸢尾属植物的化学成分和药理研究进展。 在第一和二章中分别报道了射干（Belamcanda chinensis (L.) DC.）、川射干 （Iris tectorum Maxim.）及西番莲（Passiflora incarnate L.）化学成分的分离纯化与结构鉴定。采用正、反相硅胶柱层析、凝胶柱层析、薄层制备及HPLC等各种分离方法，从三种药用植物中共分离出68个不同的化合物，其中61个的结构得 得以鉴定，另外4个化合物的结构正在鉴定中，3个由于量少且有点杂质未作进一步的鉴定。 中药射干（Rhizoma Belamcandae）为射干植物的干燥根茎，从中共分离出53个化合物，通过红外、质谱及核磁共振等波谱方法鉴定了包括12个新化合物在内的48个，结构类型分别属于iridal型三萜及其新颖的二聚体、异黄酮、黄酮及黄酮醇、香豆素、甾体、芳香酸和脂肪酸及其甘油酯等。新化合物中有两个异黄酮类化合物，其结构分别鉴定为5,7,8,4′-四羟基-6-甲氧基异黄酮和5,6-二羟基-4′-甲氧基异黄酮-7-O-β-D-吡喃葡萄糖苷；八个新的iridal型三萜化合物分别鉴定为鸢尾烯（L）、16-甲氧基鸢尾烯、16-去羟基鸢尾烯、2-(E)-16-去羟基鸢尾烯、16-去羟基鸢尾烯B、3-乙酰基-16-去羟基鸢尾烯、iristectoroneL和iristectoroneM；两个结构骨架新颖的双三萜，分别命名为射干素A和射干素B，其分离纯化的困难以及结构的新颖和复杂突显出该论文的科学意义。除这些新化合物外，还有9个已知化合物为首次从中药射干中分离得到。此外，从中药射干的代用品川射干中分离得到7个已知化合物，主要是黄酮类成分及iridal型三萜化合物，其中1个三萜化合物为从射干中分离鉴定的新成分。另外还从西番莲中分离出8个化合物，鉴定了其中的6个，主要为黄酮碳苷。 第三章是关于射干、川射干及西番莲提取物化学成分的ESI-MS-MS分析，在初步探讨了从这些植物中分离鉴定出的一些异黄酮及黄酮碳苷的质谱裂解规律基础上，通过质谱和串联质谱分析，定性和半定量地检测了射干和川射干中主要的异黄酮成分以及西番莲中的黄酮碳苷成分，为这些药材品质的快速鉴定提供了一种简便方法。 第四章概述了射干及鸢尾属药用植物的化学和药理研究进展，特别是对其中异黄酮及三萜类成分的研究进展进行了深入系统的综述。 This dissertation is composed by four chapters. The first and second chapter reports the phytochemical investigation of three medicine plants, Belamcanda chinensis (L.)DC., Iris tectorum Maxim. and Passiflora incarnate L. Sixty eight different compounds were isolated and sixty one of them were identified. The third chapter described rapid ESI-MS-MS analysis of B. chinensis, I. tectorum, and P. incarnate. The forth part is a review about the progress of studies on the chemical constituents from Belamcanda chinensis and Iris species. Fifty-three compounds were isolated from Rhizoma Belamcandae, the rhizomes of B. chinensis by the methods of column chromatography (normal and reversed phase silica gel, Sephadex LH-20), preparative TLC and HPLC. On the basis of spectroscopic methods including IR, ESI-MS, 1-D and 2-D NMR, forty eight of them were identified as seventeen flavonoids, seventeen tritepenoids, one cumarin, five steroids and some benzene derivative etc. Among them, the structures of twelve new compounds were elucidated as 6-methoxy-5,7,8,4′-tetrahydryoxyisoflavoe, 4′-methoxy-5,6-dihydroxyisoflavone-7-O-β-D-glucopyranoside, iristectorene L, 16-methoxyisoiridogermanal, 16-dehydroxyisoiridogermanal, 2-(E)-16-dehydroxy isoiridogermanal, 16-dehydroxyiristectorene B, 3-acetyl-16-dehydroxyisoiridoger- manal, iristectorone L, iristectorone M, belamcandene A and belamcandene B. Last two new compounds are dimer of triterpenoids with a novel carbon skeleton. Beside the new compounds, nine known ones were isolated from this plant for the first time. Isolation of I. tectorum yielded seven compounds. On the basis of spectroscopic methods including ESI-MS, NMR and the comparison with authentic samples, three of them were determined as isoflavone, two of them were triterpenoids, and other two were β-sitosterol and apocynin. All of them are known compounds except one of iridal type triterpenoid, 16-dehydroxyiristectorene B, which also obtained from B. chinensis as a new compound. Isolation of P. incarnate yielded eight compounds. Six of them were determined on the basis of spectroscopic methods including ESI-MS, NMR and the comparison with authentic samples. Four of them are flavone-C-gluconside, and two are steroids. The third chapter describes the tandem mass spectrometry (ESI-MS-MS) analysis of the isoflavonoids from B. chinensis and I. tectorum, as well as C-glycosyl-flavonoide from P. incarnate, in order to explore the rapid methodology of validating the quality of the herbs. In addition, the fractionation rules of some iosflavonoids and C-glycosyl-flavonoids were discussed. The fourth chapter summarizes the research development on chemistry and pharmacology of medicine plants of B.chinensis and Iris species.

一种多阳极横向场电离室

描述了一种将用于兰州放射性束流线较重离子鉴别的多阳极横向场电离室。对其性能进行了初步测试,得到该电离室有较长的坪区和较好的能量分辨。在10~4Pa的P10工作气体(10％CH_4+90％Ar)下,坪区长度为700V。对~(244)Cm α放射源,在第4片阳极对应的灵敏区域能量损失为1.30MeV,能量分辨41.1keV,相对能量分辨约3.16％。

中子星物质中的K介子凝聚

用密度相关的相对论平均场理论计算了中子星物质中的K介子凝聚 ,结果表明中子星物质发生K介子凝聚的临界密度约为 2 .75 ρ0 .中子星物质URCA过程发生的临界密度在考虑DB核物质中核子自能动量修正时为 ρρ0≈ 3.16,在不考虑DB核物质中核子自能动量修正时为 ρρ0≈ 2 .2 5 ,并进一步计算了密度相关的相对论平均场理论两种参数形式对中子星物质状态方程的影响 .

枸杞体细胞胚发生中对痕量金属离子吸收的动态研究

以药用植物宁夏枸杞 (LyciumbarbarumL .)愈伤组织为材料 ,离体培养诱导体细胞胚发生。采用多重示踪技术和γ射线能谱分析法研究枸杞体细胞胚发生中对多种痕量金属离子的吸收动态。结果表明 :( 1)体胚发生中对多种痕量金属离子的吸收呈选择性。对多重示踪剂溶液中的 2 3种核素 ,只吸收了其中的 16种 (Mn_5 2、Zn_65、Co_5 6、Co_60、As_74、Se_75、mTc_95、Rh_99、V_4 8、Rb_83、Rb_84、Sr_85、Y_87、Y_88、Zr_88和Zr_89) ,而对另 7种未吸收 (Be_7、Tc_96、Ru_97、mRh_10 1、Sc_4 6、Ga_67和Cr_5 1)。 ( 2 )吸收呈动态变化 ,在同一发育期对不同的金属离子吸收率不同 ,如第 10天 ,大部分金属离子的吸收率在 5 % /g左右 ,而Se_75、Rb_83、Sr_85和Zr_89的则是 10 %～ 3 0 % /g ;在不同发育期对同一种金属离子的吸收率不同 ,如对Se_75的吸收总体呈上升趋势。第 5天达第 1峰值 14 % /g。随后缓慢下降 ,基本稳定 ,第 15天后急剧上升 ,至第 2 0天达第 2个峰值 2 0 % /g ;随着胚性细胞的分化与分裂 ,吸收既存在一致性 ,也存在非一致性。Se_75、Rb_83、Sr_85、Co_5 6和V_4 8等核素的吸收趋势相似 ,基本上呈上升曲线。而Mn_5 2的吸收趋势则类似正态分布曲线。

用于RIBLL和CSR的气体探测的研制

气体探测器是历史最悠久的核探测器之一气体探测器具有成本低廉、制备简单、性能可靠和使用方便等特点。而且气体探测器的形状和尺寸可任意设计，厚度可随气体气压的变化而改变，适合做大面积位置灵敏、大立本角探测和有较宽的动态测量范围。所以气体探测器在各自的应用范围内发挥着巨大的作用。在兰州放射性束流线（RIBLL）上开展次级束实验的过程中，束流的定位和发散度测定都是非常重要的。我们研制了两种高性能的双维位置灵勘平行板雪崩计数器（PPAC），一种为传统的三个极板结构，另外一种为五个极板的多极结构，分别适用于较重粒子和轻粒子的位置测量。对于五个极板的多极结构的探测器，灵敏面积为100mm×100mm，采用电荷分除法读出位置，我们用3组分α源测试，工作气体选用异丁烷。测试在6.5mb气压下，位置分辨为0.55mm（FWHM），探测效率大于99.2％，位置离散小于士0.2mm。一系列的性能指标都达到了同类探测器的最好水平。该探测器和以前研制的三极板PPAC的性能均已满足RIBLL的要求，将会用作RIBLL重要的束诊元件和位置探测器。同时改进后还能在即将建成的兰州重离子加速器冷却存储环（HIRFL-CSR）上的束流诊断过程中发挥重要的作用。同时，为在RIBLL上开展超重元素和超重核素的合成实验研制了一种多阳极横向场气体电离室（MAIC）。在100mbP10气体下，对应第四块大灵敏区域，5.806MeV~(244)Cm的α粒子的能量损失为1.30MeV，得出该探测器的能量分辨为41.1keV（FwHM），相对分辨为3.16％。该探测器适合于较重粒子的鉴别，性能指标已经满足RIBLL鉴glI灼子的要求。

不同土壤水分条件下北方稻田耗水规律研究

采用田测法研究不同土壤水分条件下稻田需水规律 .试验采用淹灌、湿润灌和间歇灌 3种灌水处理 .结果表明 ,在整个生育期内由田测法测得的淹灌、湿润灌和间歇灌 3种处理的蒸散量分别为 889.1、6 35 .9和 775 .9mm ,蒸散速率分别为 6 .9、4 .9和 6 .0mm·d-1.与淹灌处理相比 ,湿润灌和间歇灌处理分别节水 2 8.5 %和 12 .7% .在充分供水的情况下 ,由Penman法计算的潜在蒸散值分别比田测法小 2 9.30 % .淹灌、湿润灌和间歇灌 3种处理的生物产量分别为 16 4 38.2 2、15 887.94和 15 75 7.88kg·hm-2 ,经济产量分别为 80 14 .0 1、782 8.91和 785 3.93kg·hm-2 .统计分析结果表明 ,3种处理间的产量差别不显著 .淹灌、湿润灌和间歇灌 3种处理的水分利用效率 (WUE)分别为 9.0 1、12 .31和 10 .12kg·hm-2 ·mm-1,淹灌的WUE分别比湿润灌和间歇灌减少 2 6 .8%和 11.0 % .对比分析结果表明 ,湿润灌的节水效果最好