160 resultados para AL-2004-1

em Chinese Academy of Sciences Institutional Repositories Grid Portal


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Self-assembled In0.9Ga0.1As, In0.9Al0.1As, and InAs quantum dots (QD) were fabricated in an InAlAs matrix lattice-matched to an InP substrate by molecular beam epitaxy. Preliminary characterizations were performed using transmission electron microscopy, photoluminescence, and reflection high-energy electron diffraction. Experimental results reveal clear differences in QD formation, size distribution, and luminescence between the InAs and In-0.9(Ga/Al)(0.1)As samples, which show the potential of introducing ternary compositions to adjust the structural and optical properties of QDs on an InP substrate. (C) 2000 American Institute of Physics. [S0021-8979(00)10213-0].

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应用电容-电压、光致荧光和深能级瞬态谱技术研究了分子束外延生长的n型Al掺杂ZnS_(1-x)Te_x外延层深中心。Al掺杂ZnS_(0.977)Te_(0.023)的光致荧光强度明显低于不掺杂的ZnS_(0.977)Te_(0.023),这表明一部分Al原子形成非辐射深中心。Al掺杂ZnS_(1-x)Te_x(x=0,0.017,0.04和0.046)的深能级瞬态傅里叶谱表明,Al引进导带下的0.21和0.39eV电子陷阱,Te除了作为材料合金的成分和等电子中心外,还涉及到一个电子陷阱的形成,其相对导带的能级位置随Te组分增加而减小。实验结果还表明仅有少量掺杂的Al原子形成非辐射中心,这说明Al对于Te组分范围内(x≤0.046)的ZnS_(1-x)Te_x外延层的确是一种非常好的施主杂质。

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1,2-聚丁二烯和3,4-聚异戊二烯是制造高性能轮胎的原料。本论文研究了以含磷化合物为第三组份的铁催化剂合成1,2-聚丁二烯和3,4-聚异戊二烯的反应规律:1.以二乙基亚磷酸酷为第三组份的铁催化剂可在己烷中,较高温度(50℃)下聚合1,3-丁二烯。通过控制催化剂组份的配比,可制备间同和无规1,2-聚丁二烯。所得间同1,2-聚丁二烯的1,2-结构含量为91%,间规度为90%;所得无规1,2-聚丁二烯的硫化胶具有优异的抗干、湿滑性能。2.以三苯基磷酸酷为第三组份的铁催化剂是合成高间同1,2一聚丁二烯的高效催化剂。所得聚合物具有高的1,2-结构含量(ca.95%),高的间规度(ca.95%)。聚合物的微观结构与催化剂组成等反应因素无关。3.以二烷基亚磷酸醋为第三组份的铁催化剂可在己烷中,较高温度(50℃)下聚合异戊二烯。二烷基亚磷酸醋中烷基影响聚合活性的顺序为乙基一甲基>正丁基>异辛基。所得聚异戊二烯的3,4(含1,2)结构含量保持在60%左右,不受反应条件的影响。4.改性甲基铝氧烷(MMAO)活化的铁催化剂聚合异戊二烯,在相当低的MMAO用量下(Al/Fe=20,摩尔比)即有高的催化活性。溶剂影响聚合活性的顺序为甲苯>环己烷>己烷>二氯甲烷。所得聚异戊二烯的3,4(含1,2)结构含量稳定在60%。

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应用光致发光(PL)、电容-电压(C-V)、深能级瞬态谱(DLTS)和光电导(PC)技术系统研究Al掺杂ZnS_(1-x)Te_x中与Al有关的类DX中心。实验结果表明,ZnS_(1-x)Te_x中存在与Ⅲ-Ⅴ族半导体DX中心相类似的性质。获得与Al有关的类DX中心光离化能E_i(~1.0eV和2.0eV)和发射势垒E_e(0.21eV和0.39eV),这表明ZnS_(1-x)Te_x大晶格弛豫的出现是由类DX中心引起。

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Photosynthesis by phytoplankton cells in aquatic environments contributes to more than 40% of the global primary production (Behrenfeld et al., 2006). Within the euphotic zone (down to 1% of surface photosynthetically active radiation [PAR]), cells are exposed not only to PAR (400-700 nm) but also to UV radiation (UVR; 280-400 nm) that can penetrate to considerable depths (Hargreaves, 2003). In contrast to PAR, which is energizing to photosynthesis, UVR is usually regarded as a stressor (Hader, 2003) and suggested to affect CO2-concentrating mechanisms in phytoplankton (Beardall et al., 2002). Solar UVR is known to reduce photosynthetic rates (Steemann Nielsen, 1964; Helbling et al., 2003), and damage cellular components such as D1 proteins (Sass et al., 1997) and DNA molecules (Buma et al., 2003). It can also decrease the growth (Villafane et al., 2003) and alter the rate of nutrient uptake (Fauchot et al., 2000) and the fatty acid composition (Goes et al., 1994) of phytoplankton. Recently, it has been found that natural levels of UVR can alter the morphology of the cyanobacterium Arthrospira (Spirulina) platensis (Wu et al., 2005b). On the other hand, positive effects of UVR, especially of UV- A (315-400 nm), have also been reported. UV- A enhances carbon fixation of phytoplankton under reduced (Nilawati et al., 1997; Barbieri et al., 2002) or fast-fluctuating (Helbling et al., 2003) solar irradiance and allows photorepair of UV- B-induced DNA damage (Buma et al., 2003). Furthermore, the presence of UV-A resulted in higher biomass production of A. platensis as compared to that under PAR alone (Wu et al., 2005a). Energy of UVR absorbed by the diatom Pseudo-nitzschia multiseries was found to cause fluorescence (Orellana et al., 2004). In addition, fluorescent pigments in corals and their algal symbiont are known to absorb UVR and play positive roles for the symbiotic photosynthesis and photoprotection (Schlichter et al., 1986; Salih et al., 2000). However, despite the positive effects that solar UVR may have on aquatic photosynthetic organisms, there is no direct evidence to what extent and howUVR per se is utilized by phytoplankton. In addition, estimations of aquatic biological production have been carried out in incubations considering only PAR (i. e. using UV-opaque vials made of glass or polycarbonate; Donk et al., 2001) without UVR being considered (Hein and Sand-Jensen, 1997; Schippers and Lurling, 2004). Here, we have found that UVR can act as an additional source of energy for photosynthesis in tropical marine phytoplankton, though it occasionally causes photoinhibition at high PAR levels. While UVR is usually thought of as damaging, our results indicate that UVR can enhance primary production of phytoplankton. Therefore, oceanic carbon fixation estimates may be underestimated by a large percentage if UVR is not taken into account.

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Submitted by zhangdi (zhangdi@red.semi.ac.cn) on 2009-04-13T11:45:31Z

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联吡陡及其衍生物不仅用于化工和药物合成的中间体,而且具有独特的赘合作用,可被用于金属催化剂配体等方面,因此它的合成方法研究引起了人们广泛的兴趣。但是非对称联吡陡的合成日前方法仍很少。本文利用己经被成功使用于其他含氮杂环的二碳合成子-1,5-二氮杂戊二烯(vinamidiniulnsalts),合成了单取代的2,2'-,2,3'-,2,4,一二类联吡陡。在合成1,5-二氮杂戊二烯的过程中:确立了一条以四甲氧基丙烷为原料一步合成l,5一二氮杂戊二烯的简捷,经济,易工业化的合成路线,并成功进行了公斤级的放大实验;优化了1,5-二氮杂戊二烯的亲电取代反应,高收率的获得溟代,硝化的1,5-二氮杂戊二烯;优化了从取代乙酸合成p取代1,5-二氮杂戊二烯的合成方法,高收率的获得九种p芳基取代1,5-二氮杂戊二烯。本文研究了非对称联吡睫合成的一种新方法:在碱性条件下,取代的1,5-二氮杂戊二烯盐各种乙酞基吡陡亲核加成的产物,不经分离直接和氨进行[3+2+1〕的成环反应,可以高收率的合成出单取代的2,2气,2,3气,2,4气三类联吡陡。这一方法己经被成功的应用于芳基取代,卤素取代,硝基取代以及无取代基的1,5-二氮杂戊二烯与三种乙酞基吡陡的反应。这种成环反应的收率与1,5-二氮杂戊二烯俘位的吸电子特征相关。因此,针对不同取代基的1,5-二氮杂戊二烯在溶剂,碱的选择以及反应温度的控制等方面进行了优化。从而成功合成出近30种单取代的非对称联吡陡。一这种合成方法,原料价格低廉,实验操作简单,而且收率高,非常适合大量合成的要求。

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Al-Li合金是近年发展起来的新型航空材料,具有低密度、高强度的特点。目前世界上正就如何进一步提高其断裂韧性,使Al-Li合金尽早走出实验室,获得实际用进行广泛,深入的研究。熔盐电解法就是在这种情况下发展起来的。虽然此法现在尚处于研究的初级阶段,但已以其能够在较简单的设备上制备低Na高纯Al-Li合金的特点受到广泛的重视,是一种很有前途的发展方向。针对我国的技术、设备现状,在参考国外研究结果的基础上,采用熔盐电解法制备Al-Li母合金 → 应用合金的制备方法是可以尽快赶上世界发步伐的有效途径。因此,本文作为整个熔盐电解制备Al-Li合金系统研究的一部分,针对目前在此领域中很多应用基础问题,诸如:作为新的电解体系正在探索中的LiCl-KCl-LiF三元相图,Li在液体Al阴极中的扩散系数,利用熔盐电解法制备低Na高纯Al-Li合金的热力学基础及如何克服LiCl强烈的吸水性给电解工艺带来的种种不便等均未得到系统研究的现状,设计完成了一系列有关熔盐电化学和热力学实验,填补了本领域的一些研究空白,并为进一步系统研究工艺条件提供了重要的参考数据。1.用NH_4Cl氯化Li_2CO_3的研究 根据热力学从理论上论证了在200 ℃左右下述氯化反应:Li_2CO_3 + 2NN_4Cl = 2LiCl + 2NH_3~↑ + H_2O~↑ + CO_2~↑可以进行完全。利用DSC方法测定反应产物LiCl的纯度,并用离子色谱法分析反应产物中CO_3~=的含量,结果均证明:在Li_2CO_3:NH_4Cl = 1:4 (mol)时,Li_2CO_3可以定量转化为LiCl,剩余的NH_4Cl完全分解。根据热重分析结果推测NH_4Cl氯化Li_2CO_3的反应历程为:Li_2CO_3 + 2NH_4Cl = 2LiCl + 2NH_3~↑ + H_2O~↑ + CO_2~↑ NH_4Cl = HCl~↑ + NH_3~↑ 而并非是想像中的:NH_4Cl = HCl~↑ + NH_3~↑ 2HCl + Li_2CO_3 = 2LiCl + H2O~↑ + CO_2~↑利用X-射线衍射方法分析产物,结果亦说明氯化可以成功。将1:4(mol)= Li_2CO_3:NH_4Cl混合样品在差热分析反应炉中直接加热测定反应产物LiCl的溶点,并与纯LiCl样品熔点的测定结果相比较,二者完全一致。以上结果说明:不仅可用此氯化反应产物代替LiCl应用于熔盐电解制备Al-Li合金中,而且还可将其应用于LiCl体系的相图测定中。因Li_2CO_3,NH_4Cl均不吸水,极易处理,因此以上研究结果无论对于Al-Li合金的工艺研究还是其他有关LiCl体系的基础研究都是很有价值的。2.直接氯化法制备LiCl-KCl-LiF三元相图的研究。LiCl-KCl-LiF三元相图是研究此体系电解机制的重要基础。为将以上直接氯化法应用于差热分析中制作此三元体系相图,首先用直接氯化法测定了三个已知二元LiCl体系相图:LiCl-KCl;LiCl-LiF;LiCl-NaCl。与文献结果吻合很好。说明将此法应用于差热分析中制作LiCl体系相图结果是可靠的。在LiCl-KCl-LiF三元相图的测定中共做出七个垂直截面,在各截面上读出等温条件下的相界点投影到浓度三角形中,得到等温投影图。结果说明LiCl-KCl-LiF是固态完全不互溶的三元共晶体系,共有三个液-固两相区;三个液-固-固三相区;一个液-固-固-固四相区,(三元共晶平面)和一个固-固-固三相区。四相点温度为348 ℃,其组成在三相平衡线的交点处,在实验上测出近似等于:41.4KCl + 57.3LiCl + 1.3LiF (mol)。3.氯化物体系中Li~+, Na~+析出电位的比较及其去极化作用的研究。在正常电化序中,Li~+应先于Na~+析出。但在以Al作阴极电解LiCl体系时,则由于Li~+在Al上有较强的去极化作用而提前析出。这是熔盐电解法可以制备低Na,高纯Al-Li合金的基础。本文在理论上对此问题进行了较深入的研究。具体内容包括(1)。测定Li~+, Na~+在二元氯化物体系中的析出电位。通过在Al阴极,Mo阴极上二离子析出电位的比较,确认了Li~+在Al阴极上产生很强的去极化作用是能利用电解法制备低Na高纯Al-Li合金的根本原因。并为在工艺研究中选择合适的电流密度提供了参考依据。(2).根据热力学理论推导出合金化反应产生的自由焓变化与去极化作用的关系:ΔG_x + ΔG_m = -nFΔE。揭示了产生去极化作用的原因。并根据ΔG_x(偏摩尔过剩自由焓)与合金结构的关系提出可以利用二元合金相图推测极化类型及极化大小。并根据动力学原理对温度对极化的影响提出了自己的看法。(3).求出合金化反应的热效应,认为在一定条件下亦可利用此值作为判断去极化作用大小的标准。(4).测定Li~+, Na~+在Al-Cu, -Al-RE合金上的析出电位。结果表明Cu,RE的存在均可加强Li~+在阴极上的去极化作用,进一步加大了Li~+, Na~+析出电位之间的差别,有利于制备更纯的Al-Li 使金。为直接生产Al-Cu-Li, Al-RE-Li三元母合金奠定了基础。(5)测定Li~+在不同组成配比的LiCl-KCl熔体中,在Al阴极上的析出电位,并求出LiCl的离子平均活度系数γ=0.71 (T = 740 ℃), 熔体对理想状态产生负偏离。4.利用阳极计时电位法测定T=720 ℃时Li在液体Al中的扩散系数D_(Li/Al) = 4.94 * 10~(-5)cm~2·s~(-1),与利用Stocks-Einstan公式计算出的理论值D_(Li/Al) = 4.85 * 10~(-5)cm~2·s~(-1)吻合较好。5.在上述理论研究的基础之上进行了工艺初探,所得初步结论有:(1).加入LiF可以提高电效。(2).采用电流密度为1 A/cm~2时,不加搅拌亦可制备出成份均匀,含Li量为10%(w.f)的Al-Li合金。(3).根据实验结果提出 Li在熔体中的熔解可能是影响电流效果的主要原因。

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对隆肛蛙属的物种构成进行了订正,建立新属肛刺蛙属Yerana gen. nov.;订正后的隆肛蛙属现仅隶2种, 即隆肛蛙F. quadrana和太行隆肛蛙F. taihangnicus。运用形态学分析探讨了隆肛蛙属物种及种群的形态差异和分类关系,通过分子系统学研究探讨了隆肛蛙属物种及种群的分类和系统发育关系,运用动物地理学方法结合系统发育关系探讨了隆肛蛙属种群的地理分布格局成因与历史过程。主要结果和推论如下: 1.隆肛蛙属物种构成的订正及一新属建立 建立新属肛刺蛙属,将隆肛蛙属中的原叶氏隆肛蛙F. yei归隶新属肛刺蛙属并更名为叶氏肛刺蛙Y. yei,,新属建立的主要依据为:(1)雄性肛部隆起,肛孔下方有两个布满黑刺的大的白色球形隆起,具单咽下内声囊, 第一指具婚刺;(2)形态量度分析表明叶氏肛刺蛙与隆肛蛙和太行隆肛蛙的形态差异远大于后两者之间的差异;(3)叶氏肛刺蛙的分布区与隆肛蛙和太行隆肛蛙的分布区距离较远且呈隔离状态;(4)分子系统学研究资料(Jiang et al.,2005)证明叶氏肛刺蛙与隆肛蛙和太行隆肛蛙非单系发生;叶氏肛刺蛙在第二支中位于基部。因此,隆肛蛙属现仅隶2种,即隆肛蛙和太行隆肛蛙。 2.隆肛蛙属种群形态学研究 对隆肛蛙属中隆肛蛙和太行隆肛蛙的15个地理种群565只标本的28项形态性状进行了测量,运用典型判别分析法对其分析的结果表明:(1)太行隆肛蛙与隆肛蛙形态差异明显,支持其为不同的物种;(2)原隆肛蛙河南伏牛山种群和山西中条山种群应为太行隆肛蛙的地理种群;(3)隆肛蛙不同地理种群之间形态差异明显,其中四川安县种群、陕西周至种群和湖北利川种群与模式产地重庆巫山种群的差异可能达到了亚种或亚种以上分化水平。对隆肛蛙属量度分析的15个种群进行定性形态分析表明其分为三种形态型,对应隆肛蛙、过渡型和太行隆肛蛙,其变异特征主要为内跗褶、雄性肛部隆起及疣粒分布、第五趾外侧缘膜等,这与量度分析结果相似。 3.隆肛蛙属种群分子系统学研究 测定隆肛蛙属Feirana的2种19种群的线粒体12S rRNA和16S rRNA基因片段、ND2基因的DNA序列,比对后共计1953bps。(1)遗传多样性与距离分析:结果表明,隆肛蛙属种群具很高的遗传多样性,19个种群样品表现出19种单倍型(遗传多样性指数Hd=1.0); ND2基因的进化信息含量远高于12SrRNA和16SrRNA。隆肛蛙属2种群组内的种群间的遗传距离远小于两种群组间的距离,种群在不同基因上的遗传距离表现的关系与对应的系统树一致。(2)系统发育关系分析:结果表明,不同基因片断基于不同方法构建的隆肛蛙属种群系统发育树结构基本一致,基本表明隆肛蛙属种群为单系发生;它们在系统树中分为两大支,分别对应于隆肛蛙和太行隆肛蛙;支持中条山种群(沁水、历山和济源种群)和伏牛山种群(栾川和内乡种群)为太行隆肛蛙的地理种群,而原隆肛蛙秦岭中东段的部分种群(柞水、宁陕、长安大坝沟种群)也应为太行隆肛蛙的地理种群。(3)亚种分化分析:根据遗传距离分析和系统发育关系分析结果,并考虑形态上的差异情况以及地理分布信息,隆肛蛙所隶种群组可分为2亚种,即隆肛蛙指名亚种F. quadrana quadrana包括四川盆地东缘大巴山东段-巫山-武陵山北麓种群和秦岭中段(周至板房子和长安广货街)种群,他们在系统关系树上聚为一支;安县亚种F. quadrana anxianensis包括四川盆地西缘岷山东麓-龙门山-大巴山和秦岭西段的种群(安县、青川、文县、南江和凤县种群),他们在系统关系树上聚为一支。太行隆肛蛙所隶种群组也可分为2亚种,即太行隆肛蛙指名亚种F. taihangnicus taihangnicus包括中条山的种群(沁水、历山和济源种群)和中东秦岭的部分种群(柞水、长安大坝沟和宁陕种群),他们在系统关系树上聚为一支;太行隆肛蛙伏牛亚种F. taihangnicus funiuensis,为伏牛山地区的种群(栾川和内乡种群),他们在系统关系树上聚为一支。 4.隆肛蛙属种群动物地理学研究 隆肛蛙属19种群的分歧年代分析: 以长江巫山段和黄河三门峡段的形成历史时期为参考点,根据已测隆肛蛙属19种群及其外群包括N. pleski、P. yunnanesis、P. robertingeri、F. limnocharis的1953bps DNA序列构建分子钟,获得各支系的分歧年代。结果表明:①棘蛙族在70Ma左右开始其独立演化历程,这与Roelants et al.(2004)的分析结果~60±15Ma左右开始分化基本一致,后者印证了本文的分子钟。②隆肛蛙属的起始分化年代较早,隆肛蛙和太行隆肛蛙两种群组的最近祖先种群大概在46Ma~50Ma左右;隆肛蛙和太行隆肛蛙种群组内的种群分化年代相对两种群组间晚得多, 隆肛蛙种群组内两亚种分化起始年代约为10Ma左右,而太行隆肛蛙种群组内两亚种分化起始年代约为6Ma。 隆肛蛙属种群分布格局形成过程分析: ①隆肛蛙属的系统关系与地理分布格局密切相关,大部分系统分支分级与地理距离成正比;②隆肛蛙属最近祖先种群的分化中心可能位于秦岭中部地区, 隆肛蛙属的种群分布格局的形成表现为隔离分化与扩散相结合的机制,由隔离分化产生的隆肛蛙祖先种群主要从秦岭中部向西南方向扩散,后隔离分化为两亚种;太行隆肛蛙祖先种群向东北方向扩散也分化为两亚种。 隆肛蛙属种群分布区域地质历史的探讨:本文所建分子钟和种群分化方式印证了该区域的几次主要地质事件,包括岷山-龙门山-西秦岭等地区的快速差异隆起、第四纪冰期等。 The specific composition of the genus Feirana should be revised. A new genus Yerana gen. nov.(Ranidae:Dicroglossinae)was established based on morphological data-set and molecular phylogeny, as a result, only two species F. quadrana and F. taihangnicus are classified into Feirana now. Morphological differences and taxonomy of populations of Feirana were investigated based on morphological and morphometric data; phylogenetic relationships and taxonomy of populations of Feirana were elucidated using molecular data, and then the proceeding of the distribution pattern of populations of Feirana were discussed. The main results and conclusions and proposals were presented as following: 1. Revising of the specific composition of the genus Feirana and establishment of a new genus The new genus Yerana, only containing the type species Y. yei, was established based on the following evidences: (1) In adult male, distinct up-heaved circular vesicle presents around the anal, and under anal there are two white balls on which black spines exist, black horny spines scatter on the upper side of first finger, and internal single subgular vocal sac presents; (2) there is obvious morphometric differences between Yerana and Feirana; (3) Yerana is distributed far from Feirana; (4) evidences of molecular phylogeny(Jiang et al.,2005)suggested that Yerana take a special phylogenetic clade which is different from other genus included in the tribe Paini. As a result, there are only two species in Feirana, i.e., F. quadrana and F. taihangnicus. 2. Morphological research of populations of Feirana Twenty-eight characters of 565 individuals of 15 populations of the genus Feirana were measured, the results of Canonical Discriminant analysis of the morphometric data-set indicated that: (1) there are very prominent differences between the two species F. quadrana and F. taihangnicus. The validity of species F. taihangnicus was approved here; (2) Mt. Funiu population and Mt. Zhongtiao population should belong to the species F. taihangnicus; (3) Obvious differences exist among 12 populations of F. quadrana, the differentiation among Zhouzhi population, Anxian population, Lichuan population, and Wushan population together with the others probably reach sub-specific or specific level. Result of morphological comparison between 15 different populations show that 3 morphological types are recogenized in according with F. quadrana, F. taihangnicus and intergradation, this result conform to the result of morphometric analysis. 3. Molecular phylogenetic study on populaions of Feirana Fragment of 12SrRNA and 16SrRNA genes, and ND2 gene of 19 populations of two species of Feirana were sequenced and aligned, from which 1953 bps were received. (1) analyses of genetic distance and hereditary diversity indicated that: genetic distance between populations in each group were less than distance between two groups of Feirana, 19 haplotypes were recognized from 19 samples of 19 populations, so the hereditary diversity of populations of Feirana was very high (Hd=1.0), phylogenetic information in ND2 gene is more than fragment sequence of 12SrRNA and 16SrRNA genes. (2) Result of molecular phylogeny indicate that the phylogenetic trees constructed using different methods based on different sequence data sets showed the revised genus Feirana is monophyletic since the 19 populations of Feirana were firstly clustered together as one large clade, which was further clustered into two major clades, corresponding to F. quadrana(GroupⅠ) and F. taihangnicus(GroupⅡ), respectively. So populations of Qinshui and Lishan in Mt. Zhongtiao, populations of Luanchuan and Neixiang in Mt. Funiu, and populations of Zhashui, Dabagou of Chang’an and Ningshan in eastern Mt. Qinling should belong to the species F. taihangnicus; (3) Subspecific differentiation. on the basis of genetic distance, phylogenetic trees and geographical distribution, F. quadrana should have two subspecies, i.e., F. quadrana qudadrana, consisting of the populations Guanghuojie of Chang’an and Zhouzhi in Mid-Mt. Qinling, populations in Wushan area and northern Mt. Wuling (Lichuan), and F. qudadrana anxianensis, consisting of the populations in eastern Mt. Ming shan-Mt. Longmen-western Mt. Daba-western Mt. Qinling (Anxian, Qingchuan, Wenxian, Nanjiang and Fengxian); F. taihangnicus should also has two subspecies, i.e., F. taihangnicus taihangnicus, consisting of the populations in Mt. Zhongtiao and eastern Mt. Qinling, and F. taihangnicus funiuensis, consisting of the populations in Mt. Funiu. 4. Zoogeography of populaions of Feirana Analysis for divergent time of 19 populations of Feirana: Using the dates of run-through of Wushan segment of Changjiang River as the time when the population of Lichuan started differentiated from the populations of Wushan and Shennongjia, and the dates of Sanmenxia segment of Yellow River as the time when the populations in Mt. Zhongtiao started differentiated from the population of Dabagou in Chang’an, molecular clock was established using sequences with 1953 bps of 19 populations of Feirana and outgroup including N. pleski, P. yunnanesis, P. robertingeri, F. limnocharis in order to estimate divergent time of all clades. Result of that indicated that: ① the tribe Paini started to evolve independently at about 70Ma when is in consistent with that estimated by Roelants et al.(2004)with result of about ~60±15Ma, they were corroborated by each other, this confirms the validity of this molecular clock; ② divergent time for speciation of Feriana is early, ancestral populations of F. quadrana and F. taihangnicus were found about 46Ma~50Ma; differentiation of populations within species is greatly late to the divergence of the two species, divergent time for F. quadrana is 10Ma and divergent time for F. taihangnicus is 6Ma. Proceeding of distribution pattern of Feirana. Phylogenetic relationships of populations of Feirana matched quite with distribution pattern of them, the relationships among clades showed in phylogenetic trees is direct ratio to geographical distance of them; the estimated date of speciation between two species of Feirana was as early as speciation of Paa yunnanesis and Nanara pleski; middle part of Mt. Qinling is the center of speciation of Feirana, combination of mult-events of dispersal and vicariance are probably the mechanism of speciation of Feirana, F. quadrana colonized the mid-Mt. Qinling and then differentiated into two subspecies in southwest direction, ancestral population of F. taihangnicus colonized the mid-Mt. Qinling and then differentiated into two subspecies in northeast direction. On geological history of the distribution of Feirana. According to molecular clock and speciation model of populations of Feirana, some geological events are confirmed, including special rise of Mt. Minshan- Mt. Longmen-western Mt. Qinling, glacial age.

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完成了19F+27Al深部非弹性碰撞产物的角分布测量.初步分析了反应产物B,C,N,O,F,Ne,Na,Mg和Al的实验室系角分布,展现出深部非弹性反应机制的特点,显示了反应系统随时间的演化过程.

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报道了高电荷态离子12 6Xeq + (6≤q≤ 30 )入射到固体Al表面产生的 2 0 0~ 10 0 0nm波段的发射光谱的实验结果。实验表明 ,在弱束流 (nA量级 )高电荷态的情况下 ,通过入射离子与固体靶的相互作用可有效地产生原子和离子的复杂组态间跃迁所形成的可见光波段的特征谱线 ,而且当入射离子的电荷剥离数超过一临界值后 (对Al,q=2 6 ) ,谱线相对强度突然显著增强。根据经典过垒模型COB(Theclassicover barriermodel) ,在入射离子的动能较小 (~ 1keV/u)的条件下 ,高电荷态离子与表面相互作用过程中电子的俘获或转移起着非常重要的作用 ,通过提高入射离子的电荷态可增强入射离子俘获电子的能力 ,显著增强激发粒子的光谱线的强度。

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用600kev的kr~+对Cr/Al薄膜系统进行了离子束混合研究。实验样品是在单晶硅上蒸镀约5000 A厚的铝膜,相继再上所需不同厚度的铬膜。Kr~+注入剂量范围在2.0 * 10~(15)~2.5 * 10~(16) kr~+/cm~2之间。用2.0 Mev的α粒子对注入前后的样品进行了背散射分析,发现铝谱的前沿和铬谱的后沿有明显的展宽,且随剂量的增大而加宽,Cr/Al界面原子混合扩展量的平方α~2注入剂量φ成线性关系;当注入剂量大于1.0 * 10~(16) kr~+/cm~2时,铝谱前沿和铬谱的后沿出现有明显的平坦,经理论拟合计算,发现有化合物形成,x射线衍射实验结果证明化合物形式为Al_(13)Cr_2。本文还得到了混合量Q与剂量的线性关系。最后,对混合机制进行了讨论

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本论文对异辛酸铁(Fe)-亚磷酸二乙酯(P)-三异丁基铝/三乙基铝(Al)催化体系进行研究, 合成熔点低于130℃的间同1,2-聚丁二烯热塑性弹性体,并且发现三异丁基铝与三乙基铝比例对聚合活性有较大的影响。放大实验合成的间同1,2-聚丁二烯熔点为126℃ ,其1,2-结构含量为84%,间同度为81%;数均分子量13万,重均分子量40万,分子量分布为3.0;300%定伸应力为14.2MPa,拉伸强度20.5MPa,扯断伸长率420%,断裂强度20.4MPa,硬度为94邵尔A,热分解温度435℃,具有良好的力学性能和热稳定性。