62 resultados para math.OA

em Chinese Academy of Sciences Institutional Repositories Grid Portal


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本文叙述一个采取以“统计模式识别”为主,以“结构模式识别”方法为辅的识别技术路线实现的以办公室自动化(OA)为应用环境的一级印刷汉字文本识别系统。该系统从实用化角度出发,采用页式文本图象扫描输入。输入后将图象文本分割成单个汉字,并根据汉字的结构特点,抽取了汉字的内层,外层,局部等多个特征。识别采用多级分类方法。识别结果形成一个国标区位码文件。系统软件建立了一种与用户间的友好界面。该系统是在IBM PC/XT上实现的,对印刷字样识别率>99%,对各类实际的办公行文其统计识别率>95%,识别速度为1~2字/秒。

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We try to connect the theory of infinite dimensional dynamical systems and nonlinear dynamical methods. The sine-Gordon equation is used to illustrate our method of discussing the dynamical behaviour of infinite dimensional systems. The results agree with those of Bishop and Flesch [SLAM J. Math. Anal. 21 (1990) 1511].

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液相中扩散传质过程研究无论对于基础理论还是生产实践都具有重要的意义.但在通常的重力环境中,传质过程不是单因素地由浓度梯度来决定,对流和沉降会对实验研究产生重要的干扰.通过光学干涉技术的应用,实现对于扩散过程中的传质系数进行测量,实验中采用Math-Zehnder干涉仪对于整个传质过程进行监控并记录相关图像信息.这些图像信息是贯穿在整个实验过程中的连续录像,不同于其它实验记录的静态图像.通过计算这些随时间改变的干涉条纹的变化,就可以推导出传质系数的结果.实验液体选用水/葡萄糖溶液,之后还将进一步将该实验装置搭载TF-1火箭,进行微重力实验,以排除重力产生的影响.

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Spectroscopic properties of Ce-doped yttrium orthoaluminate (Ce:YAlO3 or Ce:YAP) crystals grown by temperature gradient technique (TGT) were investigated, and the effects of the growth conditions on the properties were analyzed.. Methods of optical absorption (OA), photoluminescence (PL), photoluminescence decay (PLD), X-ray excited luminescence (XL) and cathodeluminescence (CL) were used in these investigations. The results showed that the absorption band peak at 202, 394 and 532 nm originated from F and F+ color center induced by the weak reducing growth atmosphere, green emission band near 500 ran derived from Ce3+ -Ce3+ pairs and band at 650 similar to 850 run from some unintentional impurity in crystals.

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本文以桃(Prunus persica L. cv. Bayuecui.)栽培种‘八月脆’和芒果(Mangifera indica L.)栽培种‘圣心’为材料,研究外源草酸对采后果实的生理生化效应及其作用机理,为果实贮藏保鲜提供新方法。采后桃果实用1、5 mM的草酸溶液浸果10 min,以浸水10 min为对照,然后在常温下贮藏,测定果实在贮藏期间对草酸处理的一些生理生化反应。芒果经采后杀菌剂(post- P)、采后草酸(post-OA)、采前+采后草酸(pre-OA + post-OA)、采前Ca + 采后草酸处理(pre-Ca + post-OA)处理,以采后浸水为对照,然后分别将果实在常温(25 C)、低温(14 C)和控制性气调(3% CO2 + 2% O2 ,14 ± 1 C)下贮藏,测定草酸处理对芒果的成熟进程、病情发展及其相关生理指标的影响。研究结果表明如下: 1.与对照相比,草酸处理的桃果实在贮藏期间果实的电解质渗漏量和呼吸速率降低、果实硬度高、果实的抗氧化酶(超氧化物岐化酶、SOD;过氧化物酶,POD;过氧化氢酶、CAT;抗坏血酸过氧化物酶、APX)和多酚氧化酶(PPO)活性提高、脂氧合酶(LOX)活性降低。同时,在贮藏后期,果实的活性氧自由基(ROS)产量(超氧阴离子、O2.;过氧化氢、H2O2)和丙二醛(MDA)含量降低。草酸的这些生理效应有利于保持膜的完整性和延缓桃果实的成熟;草酸诱导POD、SOD、PPO活性可能有助于提高采后果实的抗病性。 2.外源5、10 mM浓度的草酸(pH值中和或不中和)对芒果炭疽病原菌(Colletotrichum gloeosporioides)孢子萌发和菌丝生长均表现出显著的抑制作用。这种作用不仅与草酸降低培养基(PDA)的pH值相关,而且与草酸独特的化学特性相关。 3.在常温、低温和控制性气调贮藏下,采后草酸、采前 + 采后草酸、采前Ca + 采后草酸处理均能有效减缓芒果果实的软化速率,延缓芒果的成熟进程,降低芒果的病情指数,同时改善芒果成熟时的表皮着色,对果实完全后熟时的可溶性固形物(SSC)、可滴定酸(TA)含量、果肉口感均没有产生负面的影响。 4.草酸处理增强芒果细胞膜的稳定性,诱导提高芒果抗氧化酶活性,特别是提高果皮SOD、APX活性,降低LOX活性,以及降低果皮O2.、H2O2 和果肉H2O2含量,抑制采后果实的乙烯生物合成。这些生理生化效应与延缓芒果的成熟衰老和提高果实的抗病性相关。 5. 采后草酸、采前 + 采后草酸和采前Ca + 采后草酸处理表现出高效低廉、无毒无副作用、易操作等优点,是芒果采后贮藏保鲜的可供选、具有实际应用前景的新方法。

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Complete sets of chromosome-specific painting probes, derived from flow-sorted chromosomes of human (HSA), Equus caballus (ECA) and Equus burchelli (EBU) were used to delineate conserved chromosomal segments between human and Equits burchelli, and among four equid species, E. przewalskii (EPR), E. caballus, E. burchelli and E. zebra hartmannae (EZH) by cross-species chromosome painting. Genome-wide comparative maps between these species have been established. Twenty-two human autosomal probes revealed 48 conserved segments in E. burchelli. The adjacent segment combinations HSA3/21, 7/16p, 16q/19q, 14/15, 12/22 and 4/8, presumed ancestral syntenies for all eutherian mammals, were also found conserved in E. burchelli. The comparative maps of equids allow for the unequivocal characterization of chromosomal rearrangements that differentiate the karyotypes of these equid species. The karyotypes of E. przewalskii and E. caballus differ by one Robertsonian translocation (ECA5 = EPR23 + EPR24); numerous Robertsonian translocations and tandem fusions and several inversions account for the karyotypic differences between the horses and zebras. Our results shed new light on the karyotypic evolution of Equidae. Copyright (C) 2003 S. Karger AG, Basel.

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We have made a complete set of painting probes for the domestic horse by degenerate oligonucleotide-primed PCR amplification of flow-sorted horse chromosomes. The horse probes, together with a full set of those available for human, were hybridized onto metaphase chromosomes of human, horse and mule. Based on the hybridization results, we have generated genome-wide comparative chromosome maps involving the domestic horse, donkey and human. These maps define the overall distribution and boundaries of evolutionarily conserved chromosomal segments in the three genomes. Our results shed further light on the karyotypic relationships among these species and, in particular, the chromosomal rearrangements that underlie hybrid sterility and the occasional fertility of mules.

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Giant panda hair samples obtained by noninvasive methods served as a source of DNA for amplification of seven giant panda microsatellite loci utilizing the polymerase chain reaction. Thirteen giant pandas held in Chinese zoos were tested for identification of paternity. Some males listed as sires have been excluded as the biological father of captive-born giant pandas. Because of the death of some potential sires, paternity is still not assigned for some giant pandas, although there is a high likelihood that paternity assignment could be made if postmortem samples are available for genetic analysis. The DNA microsatellite variation assayed by the test we have developed provides a rapid, highly informative, and noninvasive method for paternity identification in giant pandas. (C) 1994 Wiley-Liss, Inc.

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We have investigated evolutionary rates of the mitochondrial genome among individuals of Madoqua kirkii using the relative rate test. Our results demonstrate that individuals of two chromosome races, East African cytotype A and Southwest African cytotype D, evolve about 2.3 times faster than East African cytotype B. Cytogenetic changes, DNA repair efficiency, mutagens, and more likely, hitherto unrecognized factors will account for the rate difference we have observed. Our results suggest additional caution when using molecular clocks in the estimation of divergence time, even within lineages of closely related taxa. Rate heterogeneity in microevolutionary timescales represents a potentially important aspect of basic evolutionary processes and may provide additional insights into factors which affect genome evolution. (C) 1995 Academic Press, Inc.

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About 336-444 bp mitochondrial D-loop region and tRNA gene were sequenced for 40 individuals of the giant panda which were collected from Mabian, Meigu, Yuexi, Baoxing, Pingwu, Qingchuan, Nanping and Baishuijiang, respectively. 9 haplotypes were found in 21 founders. The results showed that the giant panda has low genetic variations, and that there is no notable genetic isolation among geographical populations. The ancestor of the living giant panda population perhaps appeared in the late Pleistocene, and unfortunately, might have suffered bottle-neck attacks. Afterwards, its genetic diversity seemed to recover to same extent.

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To expand the feasibility of applying simple, efficient, non-invasive DNA preparation methods using samples that can be obtained from giant pandas living in the wild, we investigated the use of scent markings and fecal samples. Giant panda-specific oligonucleotide primers were used to amplify a portion of the mitochondrial DNA control region as well as a portion of the mitochondrial DNA cytochrome b gene and tRNA(Thr) gene region. A 196 base pair (bp) fragment in the control region and a 449 bp fragment in the cytochrome b gene and tRNA(Thr) gene were successfully amplified. Sequencing of polymerase chain reaction (PCR) products demonstrated that the two fragments are giant panda sequences. Furthermore, under simulated field conditions we found that DNA can be extracted from fecal samples aged as long as 3 months. Our results suggest that the scent mark and fecal samples are simple, efficient, and easily prepared DNA sources. (C) 1998 Wiley-Liss, Inc.

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The classification and phylogenetic relationships of the Old World monkeys are still controversial. For Asian colobines, from three to nine genera were recognized by different primatologists. In the present study, we have sequenced a 424 bp mitochondrial tRNA(Thr) gene and cytochrome b gene fragment from Macaca mulatta, Mandrillus sphinx, Mandrillus leucophaeus, Semnopithecus entellus, Trachypithecus vetulus, T. johnii, T. phayrei, T. francoisi, Pygathrix nemaeus, Rhinopithecus roxellanae, R. bieti, R. avunculus, Nasalis larvatus, and Colobus polykomos in order to gain independent information on the classification and phylogenetic relationships of those species. Phylogenetic trees were constructed with parsimony analysis by weighting transversions 5 or 10 fold greater than transitions. Our results support the following conclusions: (1) the Old World monkeys are divided into two subfamilies; (2) that among the colobines, Colobus, the African group, diverged first, and Nasalis and Rhinopithecus form a sister clade to Pygathrix; (3) that there are two clades within leaf monkeys, i.e. 1) S. entellus, T. johnii, and T. vetulus, and 2) T, phayrei and T. francoisi; (4) that Rhinopithecus avunculus, R. roxellanae, and R. bieti are closely related to each other, and they should be placed into the same subgenus; (5) that Rhinopithecus is a distinct genus; and (6) that the ancestors of Asian colobines migrated from Africa to Asia during the late Pliocene or early Pleistocene.

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The chemokine receptor CCR5 can serve as a coreceptor for M-tropic HIV-1 infection and both M-tropic and T-tropic SIV infection. We sequenced the entire CCR5 gene from 10 nonhuman primates: Pongo pygmaeus, Hylobates leucogenys, Trachypithecus francoisi, Trachypithecus phayrei, Pygathrix nemaeus, Rhinopithecus roxellanae, Rhinopithecus bieti, Rhinopithecus avunculus, Macaca assamensis, and Macaca arctoides. When compared with CCR5 sequences from humans and other primates, our results demonstrate that:(1) nucleotide and amino acid sequences of CCR5 among primates are highly homologous, with variations slightly concentrated on the amino and carboxyl termini; and (2) site Asp13, which is critical for CD4-independent binding of SIV gp120 to Macaca mulatta CCR5, was also present in all other nonhuman primates tested here, suggesting that those nonhuman primate CCR5s might also bind SIV gp120 without the presence of CD4. The topologies of CCR5 gene trees constructed here conflict with the putative opinion that the snub-nosed langurs compose a monophyletic group, suggesting that the CCR5 gene may not be a good genetic marker for low-level phylogenetic analysis. The evolutionary rate of CCR5 was calculated, and our results suggest a slowdown in primates after they diverged from rodents. The synonymous mutation rate of CCR5 in primates is constant, about 1.1 x 10(-9) synonymous mutations per site per year. Comparisons of K-a and K-s suggest that the CCR5 genes have undergone negative or purifying selection. K-a/K-s ratios from cercopithecines and colobines are significantly different, implying that selective pressures have played different roles in the two lineages.