122 resultados para 88-PCM-01
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本文报导了用于热缩电缆附件中间连接的一种新型填充段电应力疏散胶的配方,研究了电性能调节剂,增粘剂,填料,氨酸橡胶等对产品性能的影响.
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本文详细解释先前测量的(YSZ)ZrO_2-Y_2O_3(88:12):CeO_2(0.01,0.3,0.5wt%),Fe:O:0.03wt%+CeO_20.01wt%,CoO(0.1,0.3wt%)晶体γ辐照前后的吸收光谱。以250—310nm激发,测量这些晶体的发光光谱,定性研究不同浓度铈、钻杂质对YSZ色心发光的影响。YSZ在400—600nm色心发光因受到铈、钴杂质再吸收,使它的发光强度减弱。这种现象在γ辐照后变得更为明显。为了证实掺杂YSZ缺陷结构存在和杂质离子价态,测量了这些晶体辐照前后的电子顺磁共振。由单电荷(Y_((zr),V_n)′自由自旋和Fe~(3+)离子的ESR信号变化,反推铈、钻杂质在YSZ晶体中的价态变化。并和吸收光谱加以比较。
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Jussiaea repens L. (JRL) is an edible medicinal plant and is also used as a vegetable by the local people in southwestern China. The crude extract and its four fractions derived from JRL were evaluated for the 1,1-diphenyl-2-picrylhydrazyl radical-scavenging ability, hydroxyl radical-scavenging capacity and the potassium ferricyanide reduction property. The ethyl acetate-soluble fraction (EAF) and EAF6 (a subfraction derived from EAF) were the most valuable fraction and subfraction, respectively. Furthermore, bioactivity-guided chromatographic fractionation revealed that three pure compounds greatly contributed to the antioxidant activities. Qualitative and quantitative analyses of the major antioxidant constituents in the extract were systematically conducted by NMR, mass spectral analyses and RP-HPLC. The result demonstrated that rosmarinic acid (2.00 mg g(-1) JRL dry weight) quercetin 3-O-beta-D-glucopyranoside (9.88 mg g(-1) JRL dry weight), and kaempferol 3-O-beta-D-glucopyranoside (1.85 mg g(-1) JRL dry weight) were the major antioxidative constituents in JRL. These compounds are reported for the first time from this plant.
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Fucoxanthin was extracted from the intact rhizoid of Laminaria japonica Aresch with dimethyl sulfoxide (DMSO), and then recovered from the DMSO extract by partitioning into ethyl acetate and subsequent evaporation. Some isolation conditions such as solvent volume and extraction time were screened. The quantity and quality of the extracted fucoxanthin were determined by spectral analysis (absorption spectra and fluorescence emission spectra). The results indicated that: (1) the average total content of fucoxanthin was 122.1 mu g in 1 g of fresh L japonica rhizoid; (2) in comparison with the widely used organic solvent, acetone, DMSO was much more effective for the extraction of fucoxanthin; (3) both DMSO volume and extraction time influenced extraction efficiency such as the recovery rate and purity of fucoxanthin (1 g of fresh L. japonica rhizoid treated with 4 mL DMSO for 60 min, yielded > 88% of the total fucoxanthin with purity 0.63); (4) when (NH4)(2)SO4 concentration was in the range of 0.5- 1.0 mol/L, the pigments rapidly and entirely moved from DMSO into the ethyl acetate phase; (5) the ethyl acetate and DMSO were recycled using a rotary evaporator.
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Calreticulin (CRT), as an endoplasmic reticulum luminal resident protein, plays important roles in Ca2+ homeostasis and molecular chaperoning. CRT on the surface of the cell can modulate cell adhesion, phagocytosis and integrin-dependent Ca2+ signaling. The full length cDNA of calreticulin (FcCRT) was cloned from Chinese shrimp Fenneropenaeus chinensis. It consists of 1672 by with an open reading frame of 1221 bp, encoding 406 amino acids. This is the first reported cDNA sequence of calreticulin in Crustacea. The deduced amino acid sequence of FcCRT showed high identity with those of Bombyx mori (88%), Drosophila melanogaster (83%), Mus musculus (82%) and Homo sapiens (82%). Highest expression of FcCRT was detected in ovary by Northern blot and in situ hybridization. Different mRNA levels of FcCRT were detected at various molting stages. Expression of FcCRT was induced significantly after 3 h of heat shock treatment, reached the maximum at 4 h and dropped after that. Differential expression profiles of FcCRT were observed in hepatopancreas and haemocytes when shrimp were challenged by white spot syndrome virus (WSSV). From the above results, we inferred that FcCRT might play important roles in Ca2+ homeostasis, chaperoning and immune function in shrimp. (c) 2007 Elsevier Inc. All rights reserved.
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Peptidoglycan recognition protein (PGRP) specifically binds to peptidoglycan and plays a crucial role in the innate immune responses as a pattern recognition receptor (PRR). The cDNA of a short type PGRP was cloned from scallop Chlamys farreri (named CfPGRP-SI) by homology cloning with degenerate primers, and confirmed by virtual Northern blots. The full length of CfPGRP-SI cDNA was 1073 bp in length, including a 5 ' untranslated region (UTR) of 59 bp, a 3 ' UTR of 255 bp, and an open reading frame (ORF) of 759 bp encoding a polypeptide of 252 amino acids with an estimated molecular mass of 27.88 kDa and a predicted isoelectric point of 8.69. BLAST analysis revealed that CfPGRP-S1 shared high identities with other known PGRPs. A conserved PGRP domain and three zinc-binding sites were present at its C-terminus. The temporal expression of QPGRP-S1 gene in healthy, Vibrio anguillarum-challenged and Micrococcus lysodeikticus-challenged scallops was measured by RT-PCR analysis. The expression of CfPGRP-S1 was upregulated initially in the first 12 h or 24 h either by M. lysodeikticus or V. anguillarum challenge and reached the maximum level at 24 h or 36 h, then dropped progressively, and recovered to the original level as the stimulation decreased at 72 h. There was no significant difference between V. anguillarum and M. lysodeikticus challenge. The results indicated that the CfPGRP-S1 was a constitutive and inducible acute-phase protein which was involved in the immune response against bacterial infection. (c) 2007 Elsevier Ltd. All rights reserved.
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ISSR analysis was used to investigate genetic variations of 184 haploid and diploid samples from nine North Atlantic Chondrus crispus Stackhouse populations and one outgroup Yellow Sea Chondrus ocellatus Holmes population. Twenty-two of 50 primers were selected and 163 loci were scored for genetic diversity analysis. Genetic diversity varied among populations, percentage of polymorphic bands (PPB) ranged from 27.0 to 55.8%, H(Nei's genetic diversity) ranged from 0.11 to 0.20 and I(Shannon's information index) ranged from 0.16 to 0.30. Estimators PPB, H and I had similar values in intra-population genetic diversity, regardless of calculation methods. Analysis of molecular variance (AMOVA) apportioned inter-population and intra-population variations for C crispus, showing more genetic variance (56.5%) occurred in intra-population, and 43.5% variation among nine populations. The Mantel test suggested that genetic differentiation between nine C. crispus populations was closely related with geographic distances (R = 0.78, P = 0.002). Results suggest that, on larger distance scale (ca. > 1000 km), ISSR analysis is useful for determining genetic differentiations of C crispus populations including morphologically inseparable haploid and diploid individuals. (c) 2007 Elsevier B.V. All rights reserved.
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Morphology and culture studies on germlings of Sargassum thunbergii (Mertens et Roth) Kuntze were carried out under controlled laboratory conditions. Growth characteristics of these germlings grown under different temperatures (from 10 to 25A degrees C), irradiances (from 9 to 88 mu mol photons m(-2) s(-1)), and under blue and white light conditions are described. The development of embryonic germlings follows the classic "8 nuclei 1 egg" type described for Sargassaceae. Fertilized eggs spent 5-6 h developing into multicellular germlings with abundant rhizoids after fertilization. Under conditions of 20A degrees C, 44 mu mol photons m(-2) s(-1) and photoperiod of 12 h, young germlings with one or two leaflets reached 2-3 mm in length after 8 weeks. Temperature variations (10, 15, 20, 25A degrees C) under 88 mu mol photons m(-2) s(-1) significantly influenced the growth rate within the first week, although this effect became less obvious after 8 weeks, especially at 15 and 20A degrees C. Variation in germling growth was highly significant under different irradiances (9, 18, 44, 88 mu mol photons m(-2) s(-1)) at 25A degrees C. Low temperature (10A degrees C) reduced germling growth. Growth of germlings cultured under blue light was lower than in white light. Optimal growth of these germlings occurred at 25A degrees C and 44 mu mol photons m(-2) s(-1).
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The pyrolytic and kinetic characteristics of Enteromorpha prolifera from the Yellow Sea were evaluated at heating rates of 10, 20 and 50 degrees C min(-1), respectively. The results indicated that three stages appeared during pyrolysis; dehydration, primary devolatilization and residual decomposition. Differences in the heating rates resulted in considerable differences in the pyrolysis of E. prolifera. Specifically, the increase of heating rates resulted in shifting of the initial temperature, peak temperature and the maximum weight loss to a higher value. The average activation energy of E. prolifera was 228.1 kJ mol(-1), the pre-exponential factors ranged from 49.93 to 63.29 and the reaction orders ranged from 2.2 to 3.7. In addition, there were kinetic compensation effects between the pre-exponential factors and the activation energy. Finally, the minimum activation energy was obtained when a heating rate of 20 degrees C min(-1) was used. (C) 2009 The Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
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C-type lectins are calcium-dependent carbohydrate-binding proteins that play Important roles in innate immunity In this study, a C-type lectin homologue (SmLec1) was identified from turbot (Scophthalmus maximus) and analyzed at expression and functional levels. The open reading frame of SmLec1 is 504 bp, with a 5'-untranslated region (UTR) of 101 bp and a 3'-UTR of 164 bp The deduced amino acid sequence of SmLec1 shares 34%-38% overall identities with the C-type lectins of several fish species In silico analysis identified in SmLec1 conserved C-type lectin features, including a carbohydrate-recognition domain, four disulfide bond-forming cysteine residues, and the mannose-type carbohydrate-binding motif In addition, SmLec1 possesses a putative signal peptide sequence and is predicted to be localized in the extracellular. Expression of SmLec1 was highest in liver and responded positively to experimental challenges with fish pathogens Recombinant SmLec1 (rSmLec1) purified from yeast was able to agglutinate the Gram-negative fish pathogen Listonella anguillarum but not the Gram-positive pathogen Streptococcus uncle The agglutinating ability of rSmLec1 was abolished in the presence of mannose and ethylenediaminetetraacetic acid and by elevated temperature (65 degrees C) Further analysis showed that rSmLec1 could stimulate kidney lymphocyte proliferation and enhance the killing of bacterial pathogen by macrophages Taken together, these results suggest that SmLec1 is a unique mannose-binding C-type lectin that possesses apparent immunomodulating property and is likely to be involved in host defense against bacterial infection (C) 2010 Elsevier Ltd. All rights reserved
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Fifty-six samples of nannofossil ooze were collected from Core PC5794 in the northern equatorial Pacific at 5 em intervals. With the methods of mass spectrometer (VG354) and ICP, the Nd isotopic compositions (epsilon(Nd)(t)), Mn contents and Mg/Sr ratios of carbonate phase have been analyzed. CaCO3 contents of bulk sediments were obtained by dissolution of 0.5 mol/L HCl. Based on these data, the high-resolution epsilon(Nd)(t) profile of seawater in early Miocene with core depth(or time) have been established. The values of epsilon(Nd)(t) range from -6.2 to -2.97 and 4 fluctuation cycles existed during 24.06-22.02 Ma. 4 low epsilon(Nd)(t) values (about -6.4) correspond to high CaCO3 contents, which implicates that there were 4 cold epochs or 4 times of Antarctic Bottom Water activity. They occurred at the time of 24.06 Ma, 23.85 Ma, 22.88 Ma and 22.26 Ma, respectively. High epsilon(Nd)(t) values correspond to the high Mn contents and high values of Mg/Sr ratio, which indicates the existence of 4 intense hydrothermal activity periods during 24.06-22 Ma, the durations of them are 4.05-23.98 Ma, 23.69-23.15 Ma, 22.74-22.37 Ma and 22.06-22.02 Ma, respectively.
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The mineralogical and geochemical characteristics of Fe-oxyhydroxide samples from one dredge station (long. 103 degrees 54.48'W, lat. 12 degrees 42.30'N, water depth 2655 m) on the East Pacific Rise near lat 13 degrees N were analyzed by XRD, ICP-AES, and ICP-MS. Most Fe-oxyhydroxides are amorphous, with a few sphalerite microlites. In comparison with Fe-oxyhydroxides from other fields, the variable ranges in the chemical composition of Fe-oxyhydroxide samples are very narrow; their Fe, Si, and Mn contents were 39.90%, 8.92%, and 1.59%, respectively; they have high Cu (0.88%-1.85%) and Co (65x10(-6)-704x10(-6)) contents, and contain Co+Cu+Zn+Ni > 1.01%. The trace-element (As, Co, Ni, Cu, Zn, Ba, Sr) and major-element (Fe, Ca, Al, Mg) contents of these samples are in the range of hydrothermal sulfide from the East Pacific Rise near 13 degrees N, reflecting that this type of Fe-oxyhydroxide constitutes a secondary oxidation product of hydrothermal sulfide. The Fe-oxyhydroxide samples from one dredge station on the East Pacific Rise near 13 degrees N are lower in Sigma REE (5.44x10(-6)-17.01x10(-6)), with a distinct negative Ce anomaly (0.12-0.28). The Fe-oxyhydroxide samples have similar chondrite-normalized rare-earth-element (REE) patterns to that of seawater, and they are very different from the REE composition characteristics of hydrothermal plume particles and hydrothermal fluids, showing that the REEs of Fe-oxyhydroxide are a major constituent of seawater and that the Fe-oxyhydroxides can become a sink of REE from seawater. The quick settling of hydrothermal plume particles resulted in the lower REE content and higher Mn content of these Fe-oxyhydroxides, which are captured in part of the V and P from seawater by adsorption. The Fe-oxyhydroxides from one dredge station on the East Pacific Rise near 13 degrees N were formed by secondary oxidation in a low temperature, oxygenated environment. In comparison with the elemental (Zn, Cd, Pb, Fe, Co, Cu) average content of hydrothermal sulfide samples from the East Pacific Rise near 13 degrees N, the Zn, Cd, and Pb contents of the Fe-oxyhydroxides are lower, and their Fe, Co, and Cu contents are higher.
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该文对中国黄海和东海的蓝细菌在春、秋两季的生态分布特点进行了研究和比较,对黄海蓝细胞从10月至次年6月的生态分布进行了研究.1.东黄海海区:在秋季(2000年10月19日至11月29日)和春季(2001年3月26日至4月24日)两个季节中蓝细菌丰度在0.19~7.84×10<'4>cell/ml之间,生物量在0.56~13.74μgC/L之间,整体水平上春季比秋季高(蓝细菌的丰充与生物量平均值春季分析为4.83×10<'4>cell/ml和7.25μgC/L;秋季分别为1.72×10<'4>cell/ml和5.07μgC/L),东海比黄海高(蓝细菌生物量平均值春季黄海和东海分别为4.42μgC/L和5.52μgC/L;秋季黄海和东海分别为7.02μgC/L和7.45μgC/L).2.黄海海区:黄海蓝细菌丰度与生物量随时间变化趋势为10月至12月降低(蓝细菌丰度分别为15×10<'4>cell/ml和1.19×10<'4>cell/ml,生物量分别为4.41μgC/L和3.49×10<'4>cell/ml),4月(蓝细菌丰度与生物量分别为4.68×10<'4>cell/ml和7.02μgC/L)与12月相比有明显增高,蓝细菌丰度4月是12月的3.93倍,生物量4月是12月的2.01倍,4月至6月蓝细菌生物量大致稳定,略有增加(5月和6月蓝细菌丰度分别为5.23×10<'4>cell/ml和5.25×10<'4>cell/ml,生物量分别为7.85μgC/L和7.88μgC/L).研究发现蓝细菌在水体中的垂直分布与温度变化比较一致.
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本文以山东近海野生和养殖牙鲆Paralichthys olivaceus(T.& S.)为研究对象,采用同工酶电泳和随机扩增多态性DNA(RAPD)两种方法,进行了群体遗传学研究;另外,用PCR扩增了牙鲆、桂皮斑鲆Pseudorhombus cinnamomeus(T.& S.)、石鲽Kareius bicoloratus,Basilewsky和大菱鲆Psetta maxima 4种鲽形目鱼类mtDNA 16s rRNA基因区的部分片段,采用生物信息、学方法构建了鲽形目分子系统树。主要结果如下:1.首先建立了适于牙鲆同工酶分析的水平淀粉凝胶和垂直聚丙烯酰胺凝胶电泳系统;对获得的牙鲆15种同工酶基本酶谱进行了生化遗传分析,进而对自然和养殖群体的生化遗传结构进行了分析,共记录了29个基因座位,发现了9个多态座位。2.野生群体的生化遗传参数多态基因座位比例(31.O%)、等位基因平均数(1.38)和群体平均杂合度(0.0802)都明显高于养殖群体(24.1%,1.28,O.0788);在野生群体中有9个多态基因座位,而养殖群体仅7个多态基因座位;其中,除了Cat和Idhp-1(仅养殖群体)(P < 0.05)有显著差异、Ldh-C(P < O.01)完全偏离Hardy-Weinberg定律外,其余多态座位基因频率均符合Hardy-Weinberg遗传平衡定律。野生和养殖群体的遗传相似性系数(I)为0.9877,它们的遗传距离(D)是0.0124;两群体间的遗传分化系数G_(st)为0.0681,D_m为0.01,表明总变异中的6.8%的遗传变异产生于群体间的基因差异。3.采用11个随机引物对20个野生个体和24个养殖个体进行了RAPD群体遗传多样性分析,分别扩增出88条和86条DNA带,片段大小在200-2500bp之间,平均每个引物扩增的带数是7.8-8.0。两个群体的多态座位比例分别是43.2%和34.9%,平均杂合度是0.2739和0.2255,而Shannon遗传多样性指数表明两群体的遗传变异中有88.12%的遗传变异来自种群内,只有11.88%的变异来自群体间。遗传分化指数G_(st)的结果也验证了Shannon遗传多样性指数的结果:总群体的遗传变异中约有12%是由两群体间的基因差异产生的。4.本文对牙鲆两个群体的同一批样品分别采用经典的同工酶方法和RAPD方法进行了较系统的比较分析。发现,RAPD所显示的多态性要比同工酶的高得多,因为大部分RAPD的变异是源于非编码区和重复DNA,可以遍布整个基因组,而同工酶仅是功能基因的产物,只表现编码区的变异。因此,自然选择在同工酶编码区的作用要多于RAPD标记。在遗传相似性系数(I)和遗传距离(D)上,RAPD的分析结果与同工酶的分析结果也是有差异的,用同工酶分析两个群体遗传距离只有0.0124,而用RAPD研究可达0.0508。遗传分化指数的差异也很大,同工酶为0.0681,RAPD为0.1237。5.RAPD和同工酶的分析结果是类似的,即自然群体的多态座位比例和平均杂合度要比养殖群体高,降低幅度在同工酶中界于1.7~22.3%之间,在RAPD中则界于15.9~19.2%之间。这充分证明了养殖群体的遗传多样性水平已有明显的丧失,值得我们注意。6.构建了鲽形目鱼类mtDNA 16S rRNA基因的分子系统树。通过分子克隆法将牙鲆、桂皮斑鲆、大菱鲆和石鲽mtDNA 16S rRNA目的基因片段连接到质粒载体上,经MegaBACE测序仪测序,分别获得了590、595、582和590bp序列,通过生物信息学方法对其进行了序列分析和核酸变异比较,结合NCBI上6种鲽形目鱼类的同源序列探讨了这4种鱼类在鲽形目中的遗传分化和分子系统进化,构建了系统树,其中,桂皮斑鲆的16S rRNA基因在系统树中的位置与物种形态资料的系统演化不相符,而其它三种很好地呈现了它们在鲽形目中的系统位置。同时,可以看出mtDNA 16S rRNA基因片段可以构建一个相对准确的树,特别是NJ树和ML树比较接近,更为客观一些。由比对序列获得的物种之间的遗传距离也基本可以反映种、属、科间的不同变异水平。
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2007年夏季对黄海冷水团及邻近海域共48个站位的小型底栖动物组成、丰度和生物量,以及环境因子进行了科考研究。所调查站位的小型底栖动物平均丰度达2194 ± 1598 inds./10cm2,其中北黄海17个站位平均丰度为3408 ± 1578 inds./10cm2,南黄海31个站位平均丰度为1529 ± 1121 inds./10cm2。调查站位平均生物量为1839 ± 1289 g dwt/10cm2,其中北黄海站位平均生物量为2760 ± 1340g dwt/10cm2,南黄海平均生物量为1335 ± 902g dwt/10cm2。在分选出的共18个小型底栖动物类群中,丰度上均以自由生线虫占绝对优势,达总量的88%,且在南(88.3%)、北黄海(87.7%)基本无差异。在生物量上,同样以自由生线虫贡献最多(42%),多毛类居次(22%),其他生物量较多的还有桡足类(13%)和甲壳类幼体(12%)。在小型底栖动物的垂直分布上,分布于沉积物表层0-2cm的小型底栖动物占79%,次表层2-5cm占17%,最底层5-8cm仅占4%。统计分析表明研究站位小型底栖动物丰度和生物量与沉积物叶绿素a、有机质含量、中值粒径显著或极显著正相关,与水深呈极显著负相关,此外小型底栖动物生物量与沉积物粉砂粘土含量显著负相关。 同年秋季搭载开放航次对黄海5个站位、东海3个站位、南海2个站位的小型底栖动物组成、丰度和生物量,以及环境因子进行了调查研究。对三个海域小型底栖动物的比较研究发现,平均丰度以黄海最高,达2132 ± 946 inds./10cm2,东海次之,为1954 ± 2047 inds./10cm2,而南海仅156 ± 56 inds./10cm2;三海域的平均生物量依次为2193 ± 1148 g dwt/10cm2、1865 ± 1555 g dwt/10cm2和212 ± 22 g dwt/10cm2。在分选出的共14个小型底栖动物类群中,丰度上均以自由生线虫占绝对优势,分别占总量的85%、89%、85%。在生物量上,黄海以自由生线虫贡献最多(33%),多毛类居次(18%);东海二者比例相近(约37%),而南海则以多毛类占绝对优势(56%),线虫居次(25%)。在小型底栖动物的垂直分布上,三个海区差异较大:分布于沉积物表层0-2cm的小型底栖动物在黄海高达90%,东海仅46%,在南海为63%。统计分析表明,本研究站位小型底栖动物丰度与沉积物中的叶绿素a及脱镁叶绿素a含量和底温呈显著正相关,与水深呈显著负相关。该结果与本航次之后在广东湛江和海南以东的南海海域开展的908调查结果形成了鲜明对照,后者的小型底栖动物及线虫丰度与沉积物中有机质含量呈显著正相关,与水深呈显著负相关,表明近海受人类干扰影响较大。 本文利用微宇宙实验方法,来确定不同浓度梯度的Cu、Pb以及Cu/ Pb混合重金属污染物对青岛湾小型底栖动物(主要是线虫)的影响。加入污染物后,分别在1、3、7、14、21天进行取样分析。结果显示,Cu和Cu/Pb混合高浓度实验单元组的线虫丰度除在第21天有较明显减少外,在整个实验周期内基本没有变化,分析可能系高浓度Cu的固定作用从而使小型底栖动物无法腐烂降解造成的。同一时间尺度上,各重金属污染物实验单元的线虫丰度均高于(或接近于)空白对照组,较高浓度的重金属污染物实验单元的线虫丰度高于(或接近于)较低浓度重金属污染物实验单元,Cu/Pb混合低浓度实验单元的线虫丰度高于同一时间尺度Cu低浓度和Pb低浓度实验单元。推测是由于采样点的线虫群落中存在对Cu和Pb的耐受种或者“机会种”造成的。